Proceedings of the CITES
workshop on the conservation of
sea cucumbers in the families
Holothuriidae and Stichopodidae
,
1-3 March 2004
Kuala Lumpur
Malaysia
Edited by
Andrew W. Bruckner
U.S. Department of Commerce
National Oceanic and Atmospheric Administration
National Marine Fisheries Service
NOAA Technical Memorandum NMFS-OPR-34
August 2006
This publication should be cited as:
Bruckner, A.W. (editor). 2006. Proceedings of the CITES workshop on the conservation of sea
cucumbers in the families Holothuriidae and Stichopodidae. NOAA Technical Memorandum NMFSOPR 34 , Silver Spring, MD 244 pp.
Significant support for the development and printing of this document was provided by NOAA Fisheries,
Office of Protected Resources and NOAA’s Coral Conservation Program. The views expressed in this
document are those of the participants of the workshop, and do not necessarily reflect the official views or
policies of the U.S. Government or NOAA.
Additional copies of this publication may be requested from:
Dr. Andrew W. Bruckner
National Oceanic and Atmospheric Administration
NOAA Fisheries
Office of Habitat Conservation
1315 East West Highway
Silver Spring, MD 20910
andy.bruckner@noaa.gov
Cover photos. Upper photo: Bodaschia argus, Sulawesi Indonesia (Andy Bruckner, NOAA Fisheries) ;
lower photo: Sea cuucmbers drying on the beach, Papa New Guinea (Jeff Kinch, University of Papua New
Guinea)
Proceedings of the CITES
workshop on the conservation of
sea cucumbers in the families
Holothuriidae and Stichopodidae
Edited by Andrew Bruckner
Office of Habitat Conservation, Rm 15829
NOAA National Marine Fisheries Service
1315 East-West Highway
Silver Spring, MD 20910-3282
NOAA Technical Memorandum NMFS-OPR-34
August 2006
U.S. Department of Commerce
Carlos Gutierrez, Secretary
National Oceanic and Atmospheric Administration
Vice Admiral Conrad C. Lautenbacher, Jr., USN (Ret.)
Under Secretary for Oceans and Atmosphere
National Marine Fisheries Service
William T. Hogarth, Assistant Administrator for Fisheries
Proceedings of the CITES workshop on the
conservation of sea cucumbers in the families
Holothuriidae and Stichopodidae
Organizing Committee
Tom De Meulenaer
Alice Burke
Paula Henry
Andrew Bruckner
Working Group Leaders
Warwick Nash
Kim Friedman
Chantall Conand
Mohammad Pourkazemi
Logistical Support
Liz Burgess
James Compton
Sponsors
CITES Secretariat
Scientific Support Unit
Geneva, Switzerland
NOAA Fisheries
Office of Protected Resources
Silver Spring, MD, USA
NOAA’S Coral Reef Conservation Program
NOAA Fisheries
Office of Habitat Conservation
Silver Spring, MD, USA
Department of Fisheries Malaysia
Jalan Sultan Salahuddin
50628 Kuala Lumpur, Malaysia
Department of Wildlife and National Parks
KM 10, Jalan Cheras
56100 Kuala Lumpur, Malaysia
TRAFFIC Southeast Asia
47400 Petaling Jaya
Selangor, Malaysia
ACKNOWLEDGMENTS
The Proceedings of the CITES Workshop on the Conservation of Sea Cucumbers summarizes the outcome
of an International CITES meeting on sea cucumbers held in Kuala Lumpur, Malaysia in March 2004. This
was funded through the NOAA Coral Reef Conservation Program and NOAA Fisheries Office of Protected
Species, with additional financial and logistical support from the CITES Secretariat, TRAFFIC Southeast Asia
and the Department of Fisheries, Malaysia. The workshop was developed and conducted in response to a
Decision adopted at the 12th Conference of Parties directing the CITES Secretariat to convene a technical
workshop on sea cucumbers to review information on the biological and trade status and identify possible
conservation actions. The workshop objectives and terms of reference for the working groups were developed
by the Organizing Committee through consultations with the CITES Animals Committee working group on
sea cucumbers, and sea cucumber experts invited to the workshop. This team set the vision for the sea
cucumber workshop and worked together to develop these proceedings.
The workshop would not have been possible without the dedicated efforts of all the participants. In particular,
we wish to acknowledge the Working Group Chairs, Warwick Nash, Kim Friedman, Chantall Conand, and
Mohammad Pourkazemi, and their Rapporteurs, who presided over the deliberations during the workshop
and provided draft reports that were used in preparing this document. The success of the workshop is also
due to TRAFFIC Southeast Asia for their efforts in coordinating the logistics, including travel arrangements,
lodging, meeting facilities, and meals. We would like to thank the people behind the scenes, especially Liz
Burgess and James Compton, who were responsible for the audiovisual equipment, set-up, copying and
distribution of the materials and organization of the reception. Alice Burke and Paula Henry from the CITES
Secretariat need to be commended for all their hard work in compiling, formatting, printing and distributing the
white papers and country reports, assistance with powerpoint presentations, and compilation and distribution
of the working group reports and other materials to participants during and after the workshop. We would like
to thank The Department of Fisheries Malaysia and National Parks Peninsula Malaysia for their assistance in
logistical arrangements, their support for the reception, and their contributions through the opening address,
keynote speeches and Malaysia Country Report. Special thanks go to Alassandra Lovatelli for his efforts to
coordinate FAO efforts on sea cucumbers with CITES and this workshop, and his contributions from the
ASCAM workshop.
The background information for the participants was provided in the form of four white papers and 16 country
reports. A special thanks goes to each of the authors and speakers. Dr Chantal Conand presented a paper
and talk on Sea Cucumber Biology, Taxonomy, Distribution and Conservation Status and on Harvest
and Trade in Sea Cucumbers. This was followed by Dr. Andrew Bruckner, who discussed Management
and Conservation Strategies and Practices for Sea Cucumbers and Mr. Glenn Sant, who presented a talk
on CITES and Sea Cucumbers. Country Reports were presented by Lu Xiaoping (China), Irma Hernandez
(Cuba), Veronica Toral-Granda (Ecuador), Asep Sugiharta (Indonesia), Karl Aiken (Jamaica),Shingo Fukui
(Japan), Dinorah Perezrul (Mexico), Zaidnuddin Ilias (Malaysia), Ludivina Labe (Philippines), Andrew Bruckner
(USA), and Philip Lambert (Canada).
iii
TABLE OF CONTENTS
Acknowledgments ............................................................................................................................ iii
Executive Summary .......................................................................................................................... 2
Workshop Agenda ............................................................................................................................ 7
Introduction ...................................................................................................................................... 9
Terms of Reference for Working Groups ......................................................................................... 11
Report of Working Group 1: National fisheries management ........................................................ 14
Report of Working Group 2: Priorities for international conservation and protection ..................... 20
Report of Working Group 3: Potential CITES implementation issues ........................................... 30
Background Documents .................................................................................................................. 33
Sea Cucumber Biology, Taxonomy, Distribution and Conservation Status, C. Conand .......... 33
Harvest and Trade in Sea Cucumbers, C. Conand ................................................................... 51
Management and Conservation Strategies and Practices for Sea Cucumbers, A.Bruckner ....... 74
CITES and Sea Cucumbers, G. Sant ...................................................................................... 104
Country Reports ........................................................................................................................... 122
China .................................................................................................................................... 122
Hong Komg SAR of China .................................................................................................... 135
Cuba ..................................................................................................................................... 141
Ecuador (Galapagos Islands) ................................................................................................. 145
Fiji ........................................................................................................................................ 149
Indonesia .............................................................................................................................. 153
Jamaica ................................................................................................................................. 154
Japan .................................................................................................................................... 158
Mexico ................................................................................................................................. 166
Malaysia ............................................................................................................................... 169
Philippines ............................................................................................................................. 181
United States of America ....................................................................................................... 192
Canada ................................................................................................................................. 203
Egypt .................................................................................................................................... 205
Australia ............................................................................................................................... 207
Costa Rica ............................................................................................................................ 215
Russian Far East .................................................................................................................... 217
Papua New Guinea ............................................................................................................... 218
Recommendations of Advances in Sea Cucumber Aquaculture and Management............................ 228
Appendix III. List of Participants .................................................................................................. 236
1
EXECUTIVE SUMMARY
The CITES Workshop on the Conservation of Sea Cucumbers in the Families Holothuriidae and
Stichopodidae (Kuala Lumpur, Malaysia, March 1-3, 2004) was convened to review biological, fishery and
trade information for commercially important sea cucumber species, and identify possible national, regional
and international conservation mechanisms to ensure that the harvest and trade in these species is sustainable.
The workshop was attended by 56 representatives from governments of exporting and importing countries,
universities, industry, and NGOs. On the first day, background information was presented on 1) the biology,
taxonomy and distribution of commercially important sea cucumbers species; 2) the main species in trade and
the origin, trade routes and utilization patterns; 3) current fishing practices and management options; 4)
opportunities for sustainable wild harvest and trade controls; and 5) reports from 18 participating countries.
Three concurrent working groups (WG) met to discuss (i) national fisheries management; (ii) priorities for
international conservation and protection; and (iii) potential CITES implementation issues. All participants
were requested to work together to formulate specific recommendations on conservation, fishery management
approaches and trade measures needed to conserve and sustainably manage sea cucumber resources.
The primary threat to sea cucumber populations identified by the participants at this workshop was
overexploitation to supply growing international markets for beche-de-mer and other products. Sea cucumbers
are prone to overexploitation due to their life history (e.g., limited mobility as adults, late sexual maturity,
density-dependent reproduction, and low rates of recruitment) and ease of collection (adults are large, often
diurnal, easy to detect and collect, and do not require sophisticated fishing or processing techniques). Historical
reports describe a ‘boom-and-bust’ cycle, where over-exploitation of traditional fishing grounds has prompted
fishers to expand into deeper water, move to new locations, and target less valuable species. World sea
cucumber capture fisheries increased approximately 500% between 1950 to 2000, with the largest growth
since the 1980s. Increases are largely due to:1) larger numbers of producing countries; 2) greater numbers of
species harvested; and 3) expansion of fishing activities into remote locations and deepwater habitats.
The two most urgent needs for sea cucumber conservation identified during this workshop were the development
of national fishery management plans and harmonized trade reporting. Management plans should include specific
regulations adopted through an adaptive management process, with emphasis on size limits, quotas, spatial
closures, and other mechanisms as appropriate under particular situations. These plans should also address
bycatch and habitat impacts associated with certain gear types, include development of aquaculture and restocking
programs, and involve implementation of national monitoring programs that emphasize stock assessments and
collection and analysis of fisheries data. While there was no specific endorsement for additional CITES listings,
there was recognition that certain species qualify for listing. CITES listings could offer substantial benefits by
preventing illegal trade and harvest, and ensuring that exports are sustainable. Additional CITES listings could
help promote increased partnerships with importing countries, non-gopvernment organizations and sea cucumber
experts, and provide a mechanism for comprehensive and standardized trade and quota reporting. Furthermore,
future listings could contribute to enhanced opportunities for technical assistance and capacity building and the
development of Regional Fishery Management Organizations for sea cucumbers. Implementation of additional
CITES listings would also place additional burdens on exporting and importing countries, due to permitting
requirements, paucity of information needed to make non-detriment findings, and enforcement problems
dassociated with taxonomic discrepencies and difficulties in identifying sea cucumbers, especially in a processed
state. Some of the critical information needs that could contribute to national management and facilitate successful
implementation of possible CITES listings include 1) research on taxonomy, with emphasis on identification
tools and marking schemes; 2) basic biological and ecological research; 3) improved collection, reporting and
sharing of fishery-dependent data; 4) adoption of field monitoring programs; 4) improved education, training
and dissemination of information and tools; and 5) improved enforcement capacity to address poaching and
illegal trade.
2
National Fisheries Management
Working Group 1 (WG1) evaluated fishery management options for sea cucumber and commented on their
feasibility, achievability, and relative ease in implementation. No one best management tool was identified
that was applicable to all fisheries. The participants highlighted the points that management measures need to
be practical, should be adopted to fit the particular circumstances of the fishery, should involve community
participation in the development, and should be implemented through an adaptive management process.
WG1 laid out the essential steps of an adaptive management process: 1) characterization of the fishery; 2)
application of minimum size limit; 3) evaluation of impacts of size limits (monitoring); 4) implementation of
small area closures (if catch/population data indicate the fishery is declining); 5) implementation of seasonal
closures, rotational harvest and other measures as precautionary approaches (in absence of scientific data);
6) establishment of total allowable catch (as soon as sufficient data are available); 7) continued monitoring of
the condition of stocks; and 8)reduction of TAC or implement total closures for affected species (if stocks
continue to decline) to allow recovery of stocks.
The group reviewed six possible management measures:
Minimum size was recognized as a measure to protect pre-reproductive individuals from collection, but
management and enforcement of this measure may be difficult due to extreme size/shape changes of sea
cucumbers and shrinkage during processing. Through an adaptive management process, this was
recommended as the first measure that needs to be implemented.
Areas closures were recognized as a mechanism to protect a portion of a fished population, thereby
enhancing stocks in surrounding fished areas. The effectiveness of this measure depends on the location
relative to larval transport, condition and abundance of the spawning stock within the reserve, community
support for the measure. This measure would need to be applied in areas where size limits do not appear to
be adequate to protect and restore populations in fished areas.
Total allowable catch (TAC) was identified as the most effective way to limit fishing, but limits need to
be set for each species to avoid serial depletion. This measure requires extensive fishery dependent and
independent data and a monitoring program to determine realistic quotas, and could only be applied once
monitoring programs are in place.
Gear restrictions: Bans on trawling were not supported, although efforts to minimize habitat damage
by modifying gear and efforts to protect important sea cucumber habitats (e.g., nursery areas) were
supported. Restrictions on the use of compressed air was recognized as one way to maintain deep water
populations. A complete ban on the use of compressed air was not supported, although the group
recommended depth restrictions and more education on safe diving practices.
Rotational Harvest was identified as a measure that would allow individual sea cucumbers to achieve
a larger size before being collected. The group noted that information is not currently available to determine
appropriate rotation rates, and implementation may be difficult in some areas with traditional management or
resource tenure (e.g., Fiji).
Seasonal Closures could protect reproductive stocks of sea cucumbers. However, this measure
would be difficult to implement because reproductive seasons may extend for many months and species
exhibit asynchronous spawning periods. This would be especially problematic in the IndoPacific, where
fisheries are multi-species.
Limited entry provides a way to reduce fishing effort. However the group felt that this measure may
work in developed countries, but it not feasible in countries where this measure is not socially or culturally
acceptable.
3
Priorities for International Conservation and Protection
Working Group 2 (WG2) reviewed biological and trade status of sea cucumbers and identified biogeographical
hotspots, taxa of concern, and possible conservation and management measures. A specific level of concern
was identified for each commercially important sea cucumber (e.g., high concern throughout its range; concern
in specific range countries; potential for future concern as harvest increases; no concern; and minor specific of
little commercial value), based on their commercial value, vulnerability to harvest, distribution, historical and
present status of different populations, life history, importance in world trade, and specific issues raised by
range or importing countries.
Statement of Priority
There is a high demand for sea cucumber products on the international markets This has caused the
over-exploitation of certain fisheries. Inadequate or non-existent appropriate management plans at
both national and regional levels have allowed such exploitation to take place. It is highly recommended
that relevant regional and international institutions be engaged in the preparation of management
plans. Priority actions to be taken concern trade measures, fishery assessments and basic research
studies, as well as public awareness.
WG 2 identified 41 commercial sea cucumber species in the families Holothuridae and Stichopodidae that
were commercially harvested. This includes 31 species from the western Pacific and Indian Ocean, 4 Caribbean
species, 1 tropical eastern Pacific species, and 5 temperate species. Tropical fisheries in the Indo-Pacific target
multiple species, whereas temperate fisheries are largely monospecific. The highest value species from the
tropical IndoPacific are H. scabra, H. fuscogilva, and H. nobilis; species of medium value include A. echinites,
A. miliaris and T. ananas, and low value species include B. marmorata, H. atra, H. fuscopunctata, S.
chloronotus and S. variegatus. In the Eastern Pacific, the most important sea cucumber fishery is in the
Galápagos Islands and Mexico for I. fuscus. North American fisheries target Cucumaria frondosa (Atlantic)
and P. californicus (Pacific northwest), both of which are high volume, low value species. The species with
the longest record of exploitation, and the largest amount of recent investment in aquaculture and mariculture is
A. japonicus (Family Stichopodidae).
Geographical hotspots with a high concern of overfishing were identified off east coast of Africa and the Red
Sea, Western Pacific, Asia and Central and northwestern part of South America. These hotspots included 27
countries, or approximately half of all countries with existing sea cucumber fisheries. Overfishing was also
identified as a medium or high level of concern in about half (15 species) of all commercially important species
from the western Pacific and Indian Oceans, and also for the species collected off South America and the
Galapagos. Populations of certain high value species (e.g. H. scabra, H. nobilis H. fuscogilva, T. ananas
and I fuscus) were identified as the species of highest concern. These taxa are overfished throughout much of
their range, and populations have collapsed in some locations.
Overall, the WG participants recognized that a number of sea cucumbers are overfished, but there was no
scientific evidence that sea cucumber stocks presently under exploitation were at risk of extinction. It was
noted that overexploited species reach a scarcity level that makes them uneconomic to fisheries long before
critical levels of stock failure are reached. However, there was also recognition that depletion of one high value
species from an area triggers more pressure on other medium and low value species; as long as fisheries
continue to operate in that area, rare or depleted species will continue to be collected when found.
4
WG2 highlighted the need for the development of management strategies and harmonized trade reporting.
They noted that the framework that would support sea cucumber management and reporting is in early stages
of development in most locations. Furthermore, the establishment of management strategies is hampered by 1)
a lack of basic biological and ecological information for most commercial species, 2) limited information on
existing and historic sea cucumber fisheries, and 3) an absence of harmonized reporting codes. WG2 identified
seven overarching measures that are needed, specific actions for each measure, implications of these measures
from a conservation perspective, and possible organizations that could assist in the development and
implementation of these measures. The key information needs include:
1) research on biology and ecology, with emphasis on taxonomy, population dynamics, restocking, habitat
preferences, and role of sea cucumbers in healthy ecosystems;
2) fishery dependent and independent monitoring of specific fisheries and across regions;
3) better trade reporting;
4) development of management plans that are regionally harmonized;
5) aquaculture, mariculture and restocking efforts;
6) capacity building and training in fisheries management, reporting by fishers, training for enforcement and
customs officers, and training in research and monitoring; and
7) communication and awareness.
Potential CITES Implementation Issues
Working Group 3 (WG 3) evaluated the benefits and drawbacks of a CITES Appendix II or III listing for one
or more species of sea cucumbers. They outlined measures to assist in the management and conservation of
sea cucumbers under a “no listing” and “listing “scenario and identified measures that range states should
consider if sea cucumber species are included in Appendix II or III.
WG3 recognized the significant conservation benefits associated with a CITES listing. The WG felt that a
listing would curtail illegal trade and harvest, and provide a mechanisms to ensure that exports are sustainable
through the requirement of a non-detriment finding. A listing would result in comprehensive and standardized
trade and quota reporting. A CITES listing was also recognized as an important mechanism to raise awareness,
enhance opportunities for capacity building and technical assistance, and encourage development of new
regional fishery management organizations (RFMO) for sea cucumbers.
WG3 identified major issues regarding implementation of additional CITES listings. They emphasized burdens
associated with 1) permitting requirements; 2) costs for new management planning, monitoring, and enforcement;
3) training requirements and regulatory measures that are needed to comply with CITES provisions; 4) limited
availability of data that could be applied towards non-detriment findings; 5) taxonomic issues and difficulties in
identifying taxa of sea cucumbers in trade; and 6) socioeconomic impacts to local fishing communities.
5
The WG identified a series of priorities for sea cucumbers that need to be considered by CITES Parties under
a listing and no listing scenario. If sea cucumbers are not proposed for listing, there is a need to:
1) Endorse and adopt the findings of the FAO ASCAM workshop.
2) Encourage national fisheries agencies to develop national fishery management plans with harvest
regulations, efforts to minimize bycatch, monitoring programs, and aquaculture and restocking
programs.
3) Support the formation of RFMOs for sea cucumbers.
4) Raise awareness of conservation concerns surrounding sea cucumbers in other International Fora and
Conventions.
5) Develop standardized methodologies for monitoring populations, fisheries and trade.
6) Develop universal marking and labeling schemes.
Under a listing scenario, the WG recommended:
1) Appendix III listings for I. fuscus in additional range states;
2) Appendix III listings for additional species where needed to complement national management measures;
3) possible Appendix II listing of all or a limited number of commercially traded species of sea cucumbers.
The group recognized that range states would need to consider existing laws that affect international trade;
permit systems; knowledge of species in trade and forms in which they are traded; monitoring to determine
quotas and ensure sustainable harvest and trade, and law enforcement training.
6
CONVENTION ON INTERNATIONAL TRADE IN ENDANGERED SPECIES
OF WILD FAUNA AND FLORA
___________________
CITES Technical workshop on the conservation of sea cucumbers
in the families Holothuriidae and Stichopodidae
Kuala Lumpur (Malaysia), 1-3 March 2004
AGENDA
Opening ceremony
1.
Adoption of the agenda and working programme
Session 1: Background; biology and uses of sea cucumbers
2.
Objectives of and background to the workshop
3.
Sea cucumber biology
- Taxonomy and distribution
- Biology
- Conservation status
4.
Utilization of and trade in sea cucumbers
- Utilization as food, in traditional East Asian Medicine and other uses
- Sea cucumber fisheries
- Legal trade
- Illegal, unreported and unregulated trade
- Bycatch
- Socio-economic characteristics of the trade in sea cucumbers
Session 2: Fisheries management and conservation
5.
Management and conservation strategies & practices
- Fisheries management approaches of wild harvest (minimum size limits, closed seasons, closed
areas, etc.)
- Aquaculture and Restocking
- Trade controls and enforcement, including identification of specimens in trade
7
6.
CITES and sea cucumbers
- CITES requirements and provisions
- Compliance with Article IV, making of non-detriment findings and ‘legal acquisition’ issues
- Experience with the inclusion of Isostichopus fuscus in CITES Appendix III
Session 3: Country status reports
6.1.
China
6.2.
China (Hong Kong)
6.3.
Cuba
6.4.
Ecuador
6.5.
Fiji
6.6.
Indonesia
6.7.
Jamaica
6.8.
Japan
6.9.
Malaysia
6.10.
Mexico
6.11.
Philippines
6.12.
Solomon Islands
6.13.
United States of America
6.14.
Northern Territories (Australia)
6.15.
Canada
6.16.
Egypt
Session 4: Working Groups
7.
Major findings and recommendations from the Workshop on Advances in Sea Cucumber Aquaculture and
Management (ASCAM), 14-18 October 2003, Dalian, China.
8.
Establishment of working groups: tasks, composition and reporting
9.
Working group sessions (addressing conservation strategies;` fisheries management; `national and
international measures; and potential CITES implementation issues)
Session 5: Working group reports; findings and recommendations
10. Working group reports
11. Identification of priorities and actions to secure the conservation status of sea cucumbers in the families
Holothuridae and Stichopodidae
12. Implementation of Decision 12.60 by the Animals Committee: communication and reporting to the
Conference of the Parties
13. Closure of the workshop
8
INTRODUCTION
At the 12th meeting (Santiago, 2002), the Conference of the Parties adopted Decisions 12.60 and 12.61
related to sea cucumbers within the families Holothuriidae and Stichopodidae. The CITES Secretariat was
mandated through Decision 12.61 to convene a technical workshop on the conservation of sea cucumbers in
cooperation with relevant bodies with the outcomes to be reviewed by the Animals Committee. The technical
workshop on the conservation of sea cucumbers in the families Holothuriidae and Stichopodidae was
held from 1-3 March 2004 in Kuala Lumpur, Malaysia.
The objectives of the three-day workshop were as follows:
a) to review information on the status, catches and bycatches of and trade in specimens of sea cucumbers
within the families Holothuridae and Stichopodidae; and on domestic measures for their conservation,
including considerations of the adequacy of these measures;
b) to establish conservation priorities and actions to secure the conservation status of sea cucumbers within
the families Holothuridae and Stichopodidae, addressing inter alia trade monitoring and controls, national
legislation and regulations, fisheries management options, conservation management and research,
enforcement and capacity building; and
c) to consider and review biological and trade information, and to assist in establishing conservation priorities
and actions to secure their conservation status. The workshop will deal with species that are currently not
listed under CITES, but for which CITES offers an important forum to address their conservation,
management and regulatory needs.
The workshop was conducted in English and was attended by 56 participants, bringing together
representatives of the fisheries sector, exporting and importing countries, intergovernmental organizations such
as FAO, knowledgeable non-governmental organizations, and other stakeholders and experts.
The workshop began (Session 1) with a review by Chantal Conand, Emeritus Professor, University of La
Réunion of the biology, taxonomy and distribution of sea cucumbers in the families Holothuridae and
Stichopodidae; a short description of the main species in trade; a summary of the conservation status of sea
cucumbers and the main threatsaffecting these families; and a report on the knowledge gaps and research
priorities for biology, taxonomy and conservation.
Professor Conand then followed with a presentation on the levels of harvest and trade in sea cucumbers, with
indications of recent trends in harvest and trade, main fisheries, main exporting and importing countries, sources
of sea cucumbers (i.e. wild or aquaculture), origins, bycatch, trade routes, and principal species in trade; a
description of sea cucumbers used as food, in Traditional East Asian Medicines, live aquarium trade, and other
uses, and the socio-economic aspects of the sea cucumber fishery, including relative economic importance, a
description of the chain of custody, values and prices, and market trends.
9
In Session 2, Dr Andrew Bruckner, NOAA Fisheries, U.S. Department of Commerce presented a summary
of current sea cucumber fishery practices and management options, with discussion on opportunities for
sustainable wild harvest, aquaculture, efforts to enhance wild populations and trade controls. Mr Glenn Sant,
TRAFFIC Oceania, provided a general background on the Convention on International Trade in Endangered
Species of Wild Fauna and Flora (CITES); the different implementation requireements for species of sea
cucumbers that may belisted in either Appendix II or Appendix III; and non-CITES related institutional
measures. Ms Verónica Toral-Granda, Charles Darwin Foundation Ecuador, ended the session with a
discussion of the inclusion of Isostichopus fuscus in Appendix III by Ecuador.
In Session 3, 16 country delegates presented country status reports. Delegates reported on the status,
fisheries and trade in sea cucumbers in the families Holothuriidae and Stichopodidae in their country, addressing
national policies on management, conservation and protection.
In Session 4, the major findings and recommendations from the Workshop on Advances in Sea Cucumber
Aquaculture and Management (ASCAM) held in China on 14-18 October 2003 were presented by Mr
Alessandro Lovatelli, FAO Fishery Resources Division, Italy. Three working groups were established and
tasks were assigned under the Terms of Reference at the conclusion of the session.
In Session 5, working groups conferred and then reported their findings on:
(1) National fisheries management;
(2) Priorities for international conservation and protection; and
(3) Potential CITES implementation issues.
In the last session the implementation of Decision 12.60 by the Animals Committee and the communications
and reporting to the Conference of the Parties were discussed. As defined by the objectives of the workshop,
comments were made on the preparation of a discussion paper on the biological and trade status of these sea
cucumbers to provide scientific guidance on the actions needed to secure their conservation status for
consideration at the 13th meeting of the Conference of the Parties (October 2004).
10
TERMS OF REFERENCE OF WORKING GROUPS
Working group 1: National fisheries management
Task:
1. Identify and review existing and potential national fisheries measures for conservation and management of sea
cucumbers in the families Holothuriidae and Stichopodidae.
2. Identify and prioritise elements of workable management plans, including adaptive management measures,
fishery-dependent and fishery-independent monitoring activities, and reporting.
3. Evaluate the pros and cons of the proposed fishery management measures from a biological, socio-economic
and enforceability standpoint.
4. Provide suggestions to which audiences and actors these fisheries management actions should be directed,
and to what taxa and geographical regions they could apply.
5. Formulate and prioritise recommendations and actions to ensure adequate fisheries management of sea
cucumbers in the families Holothuriidae and Stichopodidae.
Take into consideration:
• Recommendations from the FAO workshop.
• Trade characteristics: single species/multiple species; international/national and local; food/medicinal/
live; captive bred/aquaculture/wild collected; artisenal/targeted/bycatch removal;
• Management options: quotas; size limits; certification and labelling; aquaculture; restocking; gear
restrictions; licensing; MPAs and habitat protection; and
• Challenges: knowledge, costs, time, resource needs, socio-economic implications.
Outputs:
A prioritised list of fisheries management options, that should lead to better conservation and management
of sea cucumbers in the families Holothuriidae and Stichopodidae. Identify for each the pros and cons,
actors and audiences, cost and benefits, regional and taxonomic scope, and feasibility.
11
Working group 2: Priorities for international conservation and protection
1. Review the biological and trade status of sea cucumbers within the families Holothuriidae and Stichopodidae
and identify and prioritise the threats to their long-term survival.
2. Indicate the bio geographical hotspots for sea cucumbers in the families Holothuriidae and Stichopodidae,
and the taxa that are most under threat and/or require most urgently conservation attention.
3. Review approaches to regionally and internationally manage and conserve sea cucumbers in the families
Holothuriidae and Stichopodidae, taking into consideration voluntary measures, guidelines and certification,
and regional or international regulatory measures (incl. CITES). Prioritise these policies.
4. Assess biological, social and economic requirements and implications of the different policies, and recommend
actions by relevant stakeholders.
5. Provide suggestions to what taxa and geographical regions these measures should apply, and to which audiences
and stakeholders they should be directed.
Take into consideration:
• Biological and trade information on sea cucumbers in the families Holothuriidae and Stichopodidae.
• Research needs.
• The costs and benefits of different international measures and policy options in terms of implementation,
enforcement and control, social and economic impacts, resource requirements, conservation, future
utilization of the resource.
• Recommendations from the FAO workshop.
Outputs:
• A list of bio geographical ‘hot spots’ for sea cucumbers in the families Holothuriidae and Stichopodidae
• A list of taxa of conservation concern, with justifications and an indication of measures to be taken to
ensure their long-term management and conservation.
• A table listing types of measure identified (voluntary; regulatory; regional and international) with proposed
actions, and identifying for each the implications for the stakeholders, and the impact on conservation
and management of sea cucumbers in the families Holothuriidae and Stichopodidae.
12
Working group 3: Potential CITES implementation issues
Task:
1. Discuss the appropriateness and feasibility (costs and benefits) of CITES as a tool to assist in the management
and conservation of sea cucumbers in the families Holothuriidae and Stichopodidae.
2. Identify the scientific and management requirements concerning the inclusion of species of sea cucumbers in
the families Holothuriidae and Stichopodidae in the Appendices of CITES, and assess the needs to and
possibilities of range States in meeting these requirements.
3. Address options on how to handle the problem of illegal, unrecorded and unregulated trade, considering
CITES and other mechanisms.
4. Address options for enforcement, includingidentification problems for specimens of sea cucumbers in the
families Holothuriidae and Stichopodidae in trade, and how to control international trade in parts, derivatives,
and finished products.
Take into consideration:
• CITES provisions concerning trade in species included in Appendix II and III.
• Article IV of the Convention (the making of Non-detriment Findings; legal acquisition).
• Species and specimens in international trade (whole live and dried; parts and derivatives; processed
products; origins of specimens in trade) and their taxonomy.
• Identification issues, including recognition of specimens in international trade to the species level, labelling
and marking.
• Taxa and range States of particular concern.
• Controls of international trade in CITES-listed species, and CITES reporting and data gathering
requirements.
• Recommendations from the FAO workshop.
Outputs:
• An evaluation of the pros and cons of including species of sea cucumbers in the families Holothuridae
and Stichopodidae in the Appendices of CITES.
• If appropriate suggestions for further CITES activities concerning the management and conservation of
sea cucumbers in the families Holothuriidae and Stichopodidae, including geographical and species
priorities.
• A list of measures that range States should consider in case species of sea cucumbers in the families
Holothuriidae and Stichopodidae are included in Appendix III or II, indicating their feasibility,
implications for stakeholders, practical recommendations for their implementation, and an evaluation
of their costs and benefits.
13
Report from WORKING GROUP 1
National fisheries management
Participants: Warwick Nash (Chairman), Jun Akamine, Irma Alfonso, Ahmad Ali, Manfred
Altamirano, Mark Baine, Andy Bruckner, Liz Burgess (Rapporteur), Chow Wing-kuen, Ridzwan
Hashim, Dinorah Herrero, Ramli Khamis, Ludivinia Labe, Grant Leeworthy, Stephen Sly, Alvin
Wong, Suhaila Mohd. Omar, Rozeta Zaharan.
General Recommendations
1. National Management Programs
•
A number of management tools have been recommended or are in use in countries with sea cucumber
fisheries, such as minimum size, gear restrictions, spatial and seasonal closures, rotational harvest,
limited entry have biological and economic benefits. Adoption of these measures need to be considered
through an adaptive management process based on the status of the fishery, available information, and
feasibility within each location.
•
There is no one best management tool. Specific management measures that are practical and can be
adopted will depend on the particular circumstances in each fishery, with specific considerations for
tropical and temperate fisheries; number of target species; existing knowledge and capacity; and
fishery arrangements.
•
Where possible and appropriate, management development should involve community
participation, with emphasis on building a sense of community resource ownership.
•
As an initial step, three different management scenarios could be developed depending on the existing
arrangements, including:
1) open-access fisheries with little or no information on the fishery;
2) marine tenure or community-based managed areas with some knowledge of the fishery;
3) local to national managed fisheries with certain protective measures in place and methods
to obtain catch and resource data but an incomplete understanding of effectiveness of
measures and critical gaps in necessary information.
14
The essential steps of an adaptive management process could include:
1) Characterization of the fishery (number of fishers, location and amount of catch by species etc),
markets and domestic trade routes;
2) Application of minimum size limit for export;
3) Evaluation of minimum size limit on sea cucumber populations using fishery dependent data and
population assessments;
4a) If catch data and/or population data indicate the fishery is declining, small area closures would be
implemented within collection areas; or
4b) In absence of sufficient fishery dependent/independent data area closures and other options such as
seasonal closures and rotational harvest could be applied as a precautionary approach;
5) As soon as sufficient data are available, a total allowable catch should be implemented;
6) If stocks continue to decline, the implementation of total area closures for the affected species are
recommended to allow recovery of stocks; and
7) Catch data and population surveys should continue to be obtained and analyzed; for the worst case
scenario described in #7, the fishery could be reopened at precautionary levels once population
surveys indicate recovery.
•
More specific recommendations on an adaptive management process could be made on country by
country basis through an analysis of present fishery status, existing management measures, and perceived
problems using information obtained from country reports presented at ASCAM and CITES workshops,
beche-de-mer bulletin and other publications, and through expert consultations.
•
There is some information that certain sea cucumber populations and/or species are in decline and
pressures on these resources are increasing. Given the vulnerable status of these fisheries, difficulties in
obtaining critical data needed for management, and challenges in implementing protective measures to
address overexploitation, international measures such as a CITES Appendix II listing could offer
substantial benefits through the required reporting of trade statistics and the non-detriment finding
provided by this listing.
2. Resource, fishery and trade monitoring and data acquisition
•
Countries should work to implement monitoring programs with emphasis on:
1) improved collection, reporting and information sharing of fishery-dependent data on species-specific
catch, effort, sizes, locations; and
2) implementation of field monitoring programs to obtain information on cucumber distribution, densities,
and other relevant data.
15
•
Standards for reporting of exports by species and products should be encouraged. Trade routes
should be identified and if possible, they should be consolidated. Legitimate trade routes should be
encouraged to prevent the proliferation of black market trading that hampers the accurate estimation
of stock removals.
•
Wherever possible, existing monitoring programs should be encouraged to add sea cucumbers to their
purview. While the specific method used to monitor populations can vary, standardized approaches
should be utilized within individual fisheries to allow comparison of data over time, with pilot studies
undertaken to identify the optimal approach for the particular situation. Field monitoring should utilize
stratified random sampling approaches to obtain relevant information for each habitat type or zone,
with sufficient replication in as many locations as feasible.
•
Sea cucumber fishers, industry and community members should be encouraged to participate in
monitoring programs. Technical assistance should be provided in the form of training programs in
monitoring approaches, species id, and application of monitoring data towards management should be
recommended.
3. Education and capacity building
•
One of the greatest needs is for improved education, training and dissemination of resource tools to
assist in sea cucumber identification, best collection practices, reporting provisions, processing techniques,
and management approaches for all levels of the chain of custody as appropriate (e.g., local fishers,
processors, buyers, middlemen, resource managers and owners, and enforcement officials).
•
Communication networks should be encouraged, possibly through a web-based forum, with emphasis
on possible regional networks that transfer information and provide technical assistance to local
communities through some form of national/rural extension network. This could be attached to existing
networks or programs (e.g., SPC, SPREP) or involve the creation of a more specific network for
related multispecies (invertebrate) fisheries. New programs that have started since this workshop was
held are compiled in a table prepared in 2006 by Conand and Bruckner.
•
National and local advisory groups involving fishers, processors, buyers, resource owners/managers
and fisheries agencies should also be encouraged to enhance conservation and management, and
address socioeconomic needs.
4. Enforcement
•
There is an overarching need to improve enforcement capacity to address poaching and illegal trade,
and ensure that user groups adhere to adopted management measures. The specific enforcement
approach will depend on the individual circumstances and could involve national or local governments,
or communities. An effective enforcement program in developing countries is likely to require substantial
support and assistance from developed countries.
16
Output 1: Prioritised list of fisheries m anagement options
Table I
The management measures in the following table were prioritised by feasibility, achievability and
relative ease of obtaining the necessary information to implement them. The fishery management
measures in the table below may be used individually or in combination. For some species it is
likely that more than one measure will be necessary to ensure sustainability.
Priority
Measure
Recommendations
Comments
Information
needs
Minimum
size limit
(SL)
That a minimum
size limit be set,
based on size at
onset of sexual
maturity (O SM).
The SL regulation
should be based on
dried animals.
Recognizing the
difficulty of
enforcing individual
SL for each species,
two alternative
approaches are
proposed: (1) that
four size limits be
set; (2) that a SL be
set in a form of
relevance to the
trade—i.e., ban
trade in the XS
(extra small) and
perhaps S (small)
categories.
Minimum SL was identified as an
important measure to protect against
overfishing and recruitment failure if
set at a level that ensures adequate
reproduction below the SL.
Samples of each
species, spanning
the size range over
which the
transition from
immature to
sexually mature is
made, should be
taken. Sexual
condition (male,
female, immature)
should be
determined for
each animal by
inspecting the
gonad. The
maturation ogive
(an S-shaped
curve, from 0%
mature to 100%
mature with
increasing size)
should be created.
The size at 50%
maturity is then
determined, and
the minimum SL
set as slightly
above this length.
(With information
on growth and the
length-fecundity
relationship, it is
possible to use
more detailed
methods (egg-perrecruit analysis) to
determine an
appropriate SL
more precisely.)
To avoid the
wasteful harvesting
of undersized sea
cucumber it is
recommended that
communities be
educated as to the
minimum wet
length of sea
cucumber species so
that undersized sea
cucumber are not
harvested. Wet SL
should be set for
each species, based
on size at O SM.
Minimum SL based on wet weight is
impossible because of extreme
size/shape changes.
If international/regional SLs are set,
these should be regarded as minima
for each country. Each country may
choose to set higher SL to provide
further protection if desired, or if
biological analysis demonstrates this
is advisable.
Since bêche-de-mer is traded in
various forms (dried, frozen, salted,
etc) a SL for only dried product is
practical since all other forms have
variable water content and therefore
degrees of shrinkage.
Note that, under the PNG BDM FMP,
trade in portions of bêche-de-mer is
prohibited. This should be adopted so
that chopped undersized bêche-de-mer
are not sold.
A minimum SL on dried product will
not work for value-added product
(pills, meals, etc) created in-country.
This needs to be addressed. A
minimum SL is not sufficient for
species where juveniles are not
findable (i.e., the catch is only of
mature adults), (e.g., Holothuria
nobilis) but still are prone to depletion.
So SL needs to be used in combination
with other measures to constrain
fishing pressure.
17
Priority
Measure
Recommendations
Comments
Area
closures
That communities identify
good habitat for their
commercially harvested sea
cucumber species, and set
aside a portion of habitat in
a protected area for
protection of a portion of
the population to safeguard
against depletion of
spawning stock biomass.
Total
Allowable
Catch
(TAC)
That the
effectiveness and
enforceability of
a TAC for sea
cucumber be
evaluated by
reviewing its
success
elsewhere (e.g.,
in Papua New
Guinea, where a
TAC is part of
the management
plan: The TAC
should be set for
each Province
using the best
information
available.)
Information needs
In principle the idea of protecting a
portion of a fished population within
areas closed to fishing makes sense.
The effectiveness of this management
measure depends on its location with
respect to larval transport (sources
and sinks), and on planktonic larval
duration (among other things).
Information for optimal
placement and size of
protected areas is difficult
to obtain. In many
countries and locations it
will not be possible to
obtain this information. It
may be necessary (and
In areas with resource tenure, closures sufficient) to use local
knowledge on water
may have to be very small, thus
Spatial closures are
communities should be encouraged to currents and species to
best locate a closed area.
recommended as a possible identify areas with diverse, high
tool to enhance stocks in
density sea cucumber areas that could In many places it will be
necessary to obtain the
surrounding fished areas
be protected to maximize possible
approval of the local
but these need to be flexible benefits.
community in the
and developed using best
It is noted that setting aside marine
location of the reserve.
available information on
protected areas can foster within a
current flows (likely
community a sense of stewardship
‘source’ and ‘sink’ areas),
and sustainable fishery management,
sea cucumber biology, and and this may include the recommunity needs and
establishment of traditional fishery
interests.
management measures.
It is noted that a TAC may be an effective way
of controlling fishing, but may require large
amounts of monitoring for effective compliance.
A TAC may be set in two ways: (1) as a
proportion of the spawning stock biomass (e.g.,
30% in Mexico); or (2) from historical catch
records. The latter approach can only work
when there is a long time series of catch (and
catch rate) data. It is noted that a TAC is
appropriate when stock levels are in good
condition but TAC will likely be too high if
stocks have become depleted.
Method 1: Estimates of
abundance of fishable
biomass (i.e., of legal
size). These may be
obtained using area-based
(e.g., transect) methods,
or other methods where
appropriate. This is most
feasible, and likely to be
more reliable, when the
fishing areas are small (as
in Mexico).
Monitoring of catch as it happens is essential.
Implementation and compliance are likely to be
major obstacles in many countries.
A TAC would have to be set for each species to
avoid serial depletion. This is probably
impossible if using method (2) because catch
data are not often collected by species (this
applies especially to catch rates).
Method 2: From a time
series of catch data,
determine catch levels at
which harvests appear
sustainable. (This is a
very simplified approach,
but not much more may
be possible in most of the
countries.)
There may be equitability issues associated with
quotas when issued as individual quotas; or in
the case of a competitive TAC may result in
uncontrolled fishing and likely quota over-runs.
18
Priority
Measure
Recommendations
Comments
Information
needs
Pros: Some fisheries (e.g.,
U.S.) can only feasibly
involve harvest using dive
gear, as other methods
(trawling) would be more
destructive.
Cons: Trawling is the only
possible method in deep
water.
Gear
restrictions
1. Diving (SCUBA or HOOKAH):
Rotational
harvest
Rotational harvest could benefit
certain fisheries but it would have to
be used in combination with other
management tools.
Pros: Can offer biological
benefits by allowing
individuals to achieve a larger
size
Cons: Very difficult to
implement in areas with
resource tenure like Fiji,
where community-owned.
Determining
appropriate rotation
rates requires
adaptive
management (i.e.,
not feasible to
determine this
using population or
recruitment
information).
Seasonal
closures
Seasonal closures could include
closures during reproductive periods
to protect spawning stock, or closures
during other times of the year to
reduce overall effort. However
natural closures during certain periods
of the year (such annual closures
during the monsoon season) would
still be beneficial to sea cucumber
populations.
Where the reproductive
season is extended over many
months, seasonal closure
must be for reasons other than
to protect reproductive stock.
The multi-species nature of
many fisheries, and the
asynchrony of spawning
season between species,
compounds the problem. It is
noted, however, that
restricting the fishing season,
for whatever reason, provides
conservation benefits by
constraining fishing
mortality.
Where the rationale
for closure is the
spawning season,
information on
duration of the
spawning season is
needed.
Limited
entry
Limited entry provides a way to cap
effort and get information on the
fishery with required submission of
logbooks.
Cons: Not feasible to
implement in countries where
limited entry is not acceptable
for social or cultural reasons.
Requires a socioeconomic analysis
to determine
impacts and
benefits of this
approach.
Prohibition on use of compressed air
was not supported, but depth
restrictions and education on safe
diving practices are essential.
2. Trawling: A prohibition on the use
of trawl gear is not feasible, but
efforts should be directed towards
minimizing habitat damage overall
and protecting vulnerable habitats that
are important for sea cucumbers and
other species. In general, trawling
should be prohibited in any high relief
coral or rocky bottom habitat to
reduce bycatch and habitat damage to
these fragile habitats, and gear should
be as benign as possible.
19
Report from WORKING GROUP 2
Priorities for international conservation and protection
Participants: Kim Friedman (Chairman), Sufian Ahmad, Karl Aiken, Daud Awang, Chantal Conand,
Giam Choo-hoo, Allen Hansen, He Jian Xiang, Paula Henry (Rapporteur), Jeff Kinch, Alessandro
Lovatelli, Stanley Qalovaki, Yves Samyn, Glenn Sant, Yusof Sharif, Sukarno Wagiman.
Some qualifying statements to introduce the tables presented
Sea cucumber fisheries have a long history of exploitation, with records dating back to the early 18th century.
These fisheries should be viewed through 3 characteristics: multi-specific versus mono-specific; tropical versus
temperate; traditional (artisenal) versus recent (industrial).
There was no scientific evidence or perception from the working group that sea cucumber stocks presently
under exploitation were in any way at risk from extinction. Generally, sea cucumber stocks reach a scarcity
level that makes them un-economic to fish long before critical levels of stock failure are reached. The negative
effects of stock depletions are not known. The recorded ‘boom and bust’ nature of these fisheries (unregulated)
has followed recoveries and declines in stock abundance.
From an international perspective the technical committee recognized that the framework that would support
sea cucumber fisheries management and reporting is at an early stage of development for most fishing nations.
Basic biological and ecological information is still limited for most commercial species. In addition, the recorded
history of fisheries is not detailed enough to allow useful determination of sustainable catch rates.
The establishment of appropriate management for sea cucumber fisheries is generally hampered by this situation.
However, it is critical for the following measures to be seen as a priority, and for there to be some leverage
which promotes the development of management strategies and harmonised trade reporting.
Explanatory notes to describe criteria discussed when formulating the levels of concern designations
1)
2)
3)
4)
5)
High concern
Concern in certain countries of its range
Potential for future concern as harvests increase
No concern
Minor species of little commercial importance
The criteria used for designating concern levels do not relate to perceptions that stocks of sea cucumbers are
in danger of extinction. The levels 1-5 reflect concerns for more careful management and trade stabilisation.
20
+
Criteria used to designate categories 1-5 took into account the following 7 elements:
-
Commercial value;
Vulnerability to harvest and environmental fluctuations;
Geographic distribution;
Historical and present status of the different populations;
Importance in the world trade;
Concern raised by several countries; and
Knowledge of particular life strategies (e.g. slow growth) or genetic information (e.g. isolated
populations)
Output 1: Geographical Hotspots
1. East Coast of Africa and the Red Sea, including:
Egypt, Kenya, Mozambique, Somalia, Sudan, Tanzania, Yemen and the West Indian Ocean Island
countries, including Comoros, Madagascar, Seychelles
2. Western Pacific, including:
Fiji, New Caledonia, Papua New Guinea, Solomon Islands, Tonga, Vanuatu
3. Asia, including:
China, Indonesia, Malaysia, Philippines, Thailand, Viet Nam
4. Central and north western part of South America, including:
Costa Rica, Ecuador, Guatemala, Honduras, Mexico
Output 2: Main commercial holothurian species
A list of taxa of conservation concern, with an indication of measures to be taken to ensure their long-term
management and conservaton (see See Annex 1, Tables 1 and 2)
Output 3: Types of measures identified with proposed actions
A table listing types of measure identified (voluntary; regulatory; regional and international) with proposed
actions, and identifying for each the implications for the stakeholders, and the impact on conservation and
management of sea cucumbers in the families Holothuridae and Stichopodidae (see Annex 1, Table 3)
21
Statement of Priority
There is a high demand for sea cucumber products on the international market has caused the over-exploitation
of certain fisheries. Inadequate or non-existent appropriate management plans at both national and regional
levels have allowed such exploitation to take place. It is highly recommended that relevant regional and
international institutions be engaged in the preparation of management plans.
Priority actions to be taken concern trade measures, fishery assessments and basic research studies, as well as
public awareness.
22
2 Actinopyga Holothuriidae Deep
echinites*
water
redfish
2
Pacific Western PWC 71
Central, Indian IOE 51
Ocean Eastern IOE 57
3 Actinopyga Holothuriidae Stonefish Zone 2, notable in PNG fishery
lecanora
2
Pacific Western PWC 71
Central, Indian IOE 51,
Ocean Eastern IOE 57
Holothuriidae Blackfish Taxonomic confusion - species
mixing, Zone 2, susceptible to
harvest, Species found at high
densities in protected bays
(shallow water), widely
distributed
2
Pacific Western PWC 71
Central, Indian IOE 51,
Ocean Eastern IOE 57
2
Pacific Western PWC 71
Central, Indian IOE 51,
Ocean Eastern IOE 60
4 Actinopyga Holothuriidae
palauensis
2
Pacific Western PWC 71
Central, Indian IOE 51,
Ocean Eastern IOE 61
5 Bohadschia Holothuriidae
atra
3
Pacific Western PWC 71
Central, Indian IOE 51,
Ocean Eastern IOE 62
3 Bohadschia Holothuriidae Tigerfish Future species of concern, Zone
argus
2
3
Pacific Western PWC 71
IOE 63
Indian Ocean
Eastern
4 Bohadschia Holothuriidae Brown This species and B. vitiensis
marmorata *
sandfish intereported due to similarities
in appearance
3
Pacific Western PWC 71
Central, Indian IOE 51,
Ocean Eastern IOE 64
4 Bohadschia Holothuriidae Brown This species and B. marmorata
vitiensis *
sandfish intereported due to similarities
in appearance
3
Pacific Western PWC 71
Central, Indian IOE 51,
Ocean Eastern IOE 65
5 Bohadschia Holothuriidae Tigerfish
subrubra
3
Central, Indian
Ocean Eastern
4 Bohadschia Holothuriidae Chalkfish
similis
3
Pacific Western PWC 71
Central, Indian IOE 51,
Ocean Eastern IOE 67
2 Actinopyga
miliaris *
2 Actinopyga Holothuriidae Surf
mauritiana*
redfish
Taxonomic only
FAO code
NOTE: Indonesia and the
Philippines, both producers
of significant quantities of
sea cucumbers for export
have limited data available of
what is fished and the state of
stocks
REGION
CONCERN COMMENT
Commercial value
1: high; 2: medium:
3: low
COMMON NAME
FAMILY
SPECIES
* taxonomy to be revised
CONCERN LEVEL
Table 1 - Main commercial holothurian species (Stichopodidae, Holothuriidae and Cucumariidae)
Zone 1, esp. Red Sea
23
IOE 51,
IOE 66
FAO code
REGION
1: high; 2: med; 3: low
CONCERN COMMENT
Commercial value
COMMON NAME
FAMILY
SPECIES
* taxonomy to be
revised
CONCERN LEVEL
Table 1(cont) - Main commercial holothurian species (Stichopodidae, Holothuriidae and
Cucumariidae)
5 Holothuria
arenicola
Holothuriidae
3
Pacific Western PWC
Central, Indian 71,
Ocean Eastern IOE 51,
IOE 68
5 Holothuria
cinerascens
Holothuriidae
3
Pacific Western PWC
Central, Indian 71,
Ocean Eastern, IOE 51,
IOE 69
4 Holothuria
atra
Holothuriidae Lollyfish
3
4 Holothuria
coluber
Holothuriidae Snakefish
3
4 Holothuria
edulis
Holothuriidae Pinkfish
3
1 Holothuria
fuscogilva*
Holothuriidae White
teatfish
Pacific Western PWC
Central, Indian 71,
Ocean Eastern, IOE 51,
IOE 70
Pacific Western PWC
Central, Indian 71,
Ocean Eastern, IOE 51,
IOE 71
Pacific Western PWC
Central, Indian 71,
Ocean Eastern, IOE 51,
IOE 72
Pacific Western PWC
Central, Indian 71,
Ocean Eastern IOE 51,
IOE 73
Zones 1, 2, 3. Species not easily
accessible (deep water refuge
provides surrogate protection). Slow
growth and high commercial value.
Even qotas in well managed fisheries
(E. coast Australia) have been
reduced as a precautionary measure.
3 Holothuria
Holothuriidae Elephant Future species of concern, Zone 2.
fuscopunctata
trunkfish Species not easily accessible (deep
1
3
Pacific Western PWC
Central, Indian 71,
Ocean Eastern, IOE 51,
IOE 74
3
Pacific Western PWC
Central, Indian 71,
Ocean Eastern, IOE 51,
IOE 75
3
Pacific Western PWC
Central, Indian 71,
Ocean Eastern, IOE 51,
IOE 76
water refuge provides surrogate
protection).
4 Holothuria
leucospilota
Holothuriidae
5 Holothuria
impatiens
Holothuriidae
low commercial value - some concern
in Madagascar.
24
1 Holothuria
nobilis*
(H. whitmaei
in EIO and
Pacific)
Holothuriidae Black
teatfish
1 Holothuria
scabra
Holothuriidae Sandfish
2 Holothuria
scabra var.
versicolor*
Holothuriidae Golden
sandfish
FAO code
REGION
1: high; 2: med; 3: low
CONCERN COMMENT
Commercial value
COMMON NAME
FAMILY
SPECIES
* taxonomy to be
revised
CONCERN LEVEL
Table 1(cont) - Main commercial holothurian species (Stichopodidae, Holothuriidae and
Cucumariidae)
Zones 1, 2, 3. Susceptible easily
accessed shallow water stock of
concern. Slow growing species found at
low densities. Even in well managed
fisheries (e.g. East coast Australia) the
quota has needed to be withdrawn
pending further studies.
Zones 1, 2, 3. Susceptible shallow water
stock (studies presently planned to
investigate for deeper water stocks in
Australia). Muddy bottom species easily
targeted. Can be found at high densities.
Subject to population fluctuations due to
environmental location. Genetically
isolated populations found on relatively
small scales. Represents most of the
global market. Aquaculture potential.
Evidence of localised economic
depletions found across Pacific,
Madagascar, Tanzania, Red Sea.
Australia presents a contrary view with
a stable fishery at 200-300 metric tonnes
(wet weight) per annum.
1
Pacific
Western
Central,
Indian
Ocean
Eastern,
PW C
71,
IOE
51,
IOE
77
1
Pacific
Western
Central,
Indian
Ocean
Eastern,
PW C
71,
IOE
51,
IOE
78
Zone 2. More information needed for
other zones. Catches of this species are
often reported under sandfish. Has a
high commercial value.
1
Pacific
Western
Central,
Indian
Ocean
Eastern,
Pacific
Western
Central,
Indian
Ocean
Eastern,
PW C
71,
IOE
51,
IOE
79
PW C
71,
IOE
51,
IOE
80
Pacific
Western
Central,
Indian
Ocean
Eastern,
Pacific
Western
Central,
Indian
Ocean
Eastern,
PW C
71,
IOE
51,
IOE
81
PW C
71,
IOE
51,
IOE
82
4 Pearsonothuria Holothuriidae Flowerfish
graeffei
3
2 Stichopus
chloronotus
Stichopodidae Greenfish Future species of concern, Zone 2.
Value increasing.
2
2 Stichopus
herrmanni *
Stichopodidae Curryfish Zones 1, 3. Future concern in Zone 2.
Found in protected waters, easily fished,
problems with processing.
2
(formerly
S. variagatus)
25
2 Stichopus
horrens
Stichopodidae Dragonfish Zones 3, especially in parts of
Malaysia and Thailand.
3
1 Thelenota
ananas
Stichopodidae Prickly
redfish
1
3
4
3
5
4
Zones 1, 2, 3. Large species of
medium to high value.
Susceptible due to low
fecundity and late sexual
maturity.
Thelenota anax Stichopodidae Amberfish Potential replacement of
higher value species.
Thelenota
Stichopodidae
Large species; poorly known
rubralineata
Athyonidium Cucumariidae
More info needed. Recent
chilensis
non-traditional fishery.
Stichopus
Stichopodidae
mollis
Apostichopus Stichopodidae
japonicus
3 Cucumaria
frondosa
4 Actinopyga
agassizi
4 Holothuria
mexicana
4 Astichopus
multifidus
3 Isostichopus
badionotus
3
REGION
FAO code
PWC 71
IOE 51,
IOE 83
PWC
71, IOE
51, IOE
84
Pacific Western PWC 71
Pacific Southeast PSE 87
1
Future concern
2
Concern in Ecuador,
(Galapagos) and Mexico.
Note small range. Generally
mono species fishery without
other options for fishers. Pls
refer to Doc. 6.4
2
Cucumariidae
2
Holothuriidae
3
Holothuriidae
3
Stichopodidae
3
Stichopodidae
3
26
Pacific Western
Central, Indian
Ocean Eastern,
Indian Ocean
Eastern
Pacific Western
Central, Indian
Ocean Eastern,
2
4 Parastichopus Stichopodidae
parvimensis
3 Parastichopus Stichopodidae
californicus
Stichopodidae
1 Isostichopus
fuscus
1: high; 2: med; 3: low
CONCERN COMMENT
Commercial value
COMMON NAME
FAMILY
SPECIES
* taxonomy to be
revised
CONCERN LEVEL
Table 1(cont) - Main commercial holothurian species (Stichopodidae, Holothuriidae and
Cucumariidae)
Pacific
Southwest
Pacific
Northwest
PSW 81
PNW 61
Pacific Eastern
Central
PEC 77
Pacific Eastern
Central
Pacific Eastern
Central
PEC 77
PEC 77
ANW
Atlantic
21
Northwest
Atlantic Western AWC
31
Central
Atlantic Western AWC
31
Central
Atlantic Western AWC
31
Central
Atlantic Western AWC
31
Central
CONCERN
LEVEL
Table 2. Main commercial holothurian species from concern levels 1, 2 and 3 (see Table 1)
SPECIES
* taxonomy
to be
revised
FAMILY
1
Holothuria
fuscogilva*
Holothuriidae
1
Holothuria
nobilis*
Holothuriidae
1
Holothuria
scabra
Holothuriidae
1
Thelenota
ananas
Stichopodidae
1
Isostichopus
fuscus
Stichopodidae
2
Actinopyga
echinites*
Holothuria
scabra
versicolor*
Holothuriidae
2
Actinopyga
lecanora
Holothuriidae
2
Actinopyga
miliaris*
Holothuriidae
2
Holothuriidae
MEASURES THAT COULD BE TAKEN
High level of concern. Generally overfished. Exporting countries
need to have a regionally harmonised national management plan for
this species. Need Internationally harmonised reporting codes for
export. Priority given to this species for basic biological and
ecological research and stock assessments.
High level of concern. Generally overfished. Exporting countries
need to have a regionally harmonised national management plan for
species. Need Internationally harmonised reporting codes for
export. Priority given to this species for basic biological and
ecological research and stock assessments.
High level of concern. Generally overfished. Exporting countries
need to have a regionally harmonised national management plan for
this species. Need Internationally harmonised reporting codes for
export. Priority given to this species for basic biological and
ecological research and stock assessments.
High level of concern. Generally overfished. Exporting countries
need to have a regionally harmonised national management plan for
this species. Need Internationally harmonised reporting codes for
export. Priority given to this species for basic biological and
ecological research and stock assessments.
High level of concern. Generally overfished. Exporting countries
need to have a regionally harmonised national management plan for
this species. Need Internationally harmonised reporting codes for
export. Priority given to this species for basic biological and
ecological research and stock assessments.
Compare taxonomic differences in Indian and Pacific populations.
Medium level of concern. Catches difficult to determine. Exporting
need to have a regionally harmonised national management plan for
this species. Need Internationally harmonised reporting codes for
export. Priority given to this species for basic biological and
ecological research and stock assessments.
Medium level of concern. Overfishing becoming more widespread.
Exporting countries need have a regionally harmonised national
management plan for this species. Internationally harmonised
reporting codes for export need to be adopted. Priority given to this
species for basic biological and ecological research.
Medium level of concern. Overfishing becoming more widespread.
Exporting countries to have a regionally harmonised national
management plan for this species. Internationally harmonised
reporting codes for export need to be adopted. Priority given to this
species for basic biological and ecological research.
27
CONCERN
LEVEL
Table 2 (cont) Main commercial holothurian species from concern levels 1, 2 and 3.
SPECIES
* taxonomy
to be revised
FAMILY
2
Actinopyga
mauritiana
Holothuriidae
2
Stichopus
herrmanni *
Stichopodidae
2
Stichopus
horrens
Stichopodidae
2
Stichopus
chloronotus
Stichopodidae
3
Bohadschia
argus
Holothuriidae
3
Holothuria
fuscopunctata
Holothuriidae
3
Parastichopus
californicus
Stichopodidae
3
Isostichopus
badionotus
Stichopodidae
MEASURES THAT COULD BE TAKEN
Medium level of concern. Overfishing becoming more widespread.
Exporting countries to have a regionally harmonised national
management plan for this species. Internationally harmonised
reporting codes for export adopted. Priority given to this species
for basic biological and ecological research.
Medium level of concern. Overfishing becoming more widespread.
Exporting countries to have a regionally harmonised national
management plan for this species. Internationally harmonised
reporting codes for export adopted. Priority given to this species
for basic biological and ecological research.
Medium level of concern. Overfishing becoming more widespread.
Exporting countries to have a regionally harmonised national
management plan for this species. Internationally harmonised
reporting codes for export adopted. Priority given to this species
for basic biological and ecological research.
Medium level of concern. Overfishing becoming more widespread.
Exporting countries to have a regionally harmonised national
management plan for this species. Internationally harmonised
reporting codes for export adopted. Priority given to this species
for basic biological and ecological research.
Future concern. Overfishing present once higher value species
depleted. Exporting countries to have a regionally harmonised
national management plan for this species. Internationally
harmonised reporting codes for export adopted. Priority given to
this species for basic biological and ecological research.
Future concern. Overfishing present once higher value species
depleted. Exporting countries to have a regionally harmonised
national management plan for this species. Internationally
harmonised reporting codes for export adopted. Priority given to
this species for basic biological and ecological research.
Future concern. Overfishing present once higher value species
depleted. Exporting countries to have a regionally harmonised
national management plan for this species. Internationally
harmonised reporting codes for export adopted. Priority given to
this species for basic biological and ecological research.
Future concern. Overfishing present once higher value species
depleted. Exporting countries to have a regionally harmonised
national management plan for this species. Internationally
harmonised reporting codes for export adopted. Priority given to
this species for basic biological and ecological research.
28
Table 3. The types of measures identified (voluntary; regulatory; regional and international) with
proposed actions, implications for the stakeholders, and the impact on conservation and
management of Sea cucumbers in the families Holothuridae and Stichopodidae
IMPLICATION FOR
MEASURE
DETAILED ACTION
POSSIBLE BODY
STAKEHOLDERS
FOR ACTION OR
ASSISTANCE
Trade definition/legal
Basic biology
Taxonomic research
Global Taxonomic
definitions. Distribution
ecology
Initiative, National
awareness. Design of
and regional Bodies
MPA’s
University
Understanding of species
Population parameters
vulnerability in order to
(larval, recruitment,
design appropriate
growth, mortality)
management strategies
Restocking issues
WORLDFISH
Habitat understanding &
IRD, WIOMSA
effects of sea cucumber
removal
Fishery
Design improvement &
SPC, CSIRO,
Allow comparisons
assessment
Harmonization of
GBRMPA, FAO,
across regions of fishery
(Density and
methodology
WIOMSA
experience
biomass, indirect Case study reports (both
SPC, USP, FAO,
Potential of
measures, MSY) good &bad)
WIOMSA
understanding of carrying
capacity & TAC settings
Trade measures
Harmonization of trade
CITES, FAO,
Understanding catch and
reporting
WIOMSA
trends and commercial
activity
Trade bulletins
Understanding the
market
Stock awareness,
FAO, SPC, Other
Fisheries
Management plans with
achieving optimal
regional fisheries
management
regionally harmonized
sustainability
bodies
comparable data
collection
Short- to medium-term
economic hardship
WORLDFISH
Research into restocking
effects
Capacity
Management plans
FAO, SPC,
building
Post harvest for fishers
SPC, FAO WIOMSA
Management training for
national administrators
Training of customs /
CITES
clearance officers
Research and assessment WIOMSA
training
SPC, CITES
Communication
Educational training
and awareness
material for fishers/
administrator
Trade bulletin
29
Report from WORKING GROUP 3
Potential CITES implementation issues
Participants: Mohammad Pourkazemi (Chariman), Tom De Meulenaer (Rapporteur), John Field, Shingo
Fukui, Gilbert Hanson, Zaidnuddin Ilias, Kwan Sai-ping, Philip Lambert, Ahmad Saktian Langgang,
Andrew Lawrence, Loo Kean Seong, Lu Xioaping, Azhar Noraini, David Pawson, Sim Yee Kwang,
Asep Sugiharta, Veronica Toral, Thalathiah Saidin, Zaihatun Mahani Zakaria.
Output 1: An evaluation of the pros and cons of including species of sea cucumbers in the families
Holothuriidae and Stichopodidae in the Appendices of CITES
Pros:
1. Curtail illegal trade and harvest
2. Requirement for ensuring exports are sustainable (Appendix II)
3. Cessation of overharvest /perpetuation of sustainable fisheries
4. Awareness raising amongst stakeholders and decision-makers
5. Enhanced opportunities for technical assistance and capacity building
6. Could help address FAO concerns about overexploitation, as expressed in the ASCAM workshop
(October 2003, Dalian, China)
7. Listing in Appendix II or III can assist in the conservation and management of sea cucumber species
for long-term socioeconomic benefits from sustainable fisheries
8. Regulatory measures to comply with CITES provisions
9. Comprehensive and standardized trade and quota reporting, to species level
10. May encourage the development of new Regional Fishery Management Organizations (RFMO’s) for
sea cucumbers
Cons:
1. Burden on both range countries and importing countries
• Permitting requirements
• Institutional infrastructure to deal with new CITES trade (e.g., cost of management planning, monitoring
programs, new research initiatives, development of new legislation, elevated wildlife inspection)
• New training required for trade interdiction and specimen ID
• New set of non-detriment findings with little data
• Regulatory measures to comply with CITES provisions
30
2. Short-term socio-economic impacts
• Reduction in fisheries income
• Reduction in tax revenue
• Disruption of local fishing communities
3. Potential to diminish cooperation in market surveys, IUU trade investigations
Output 2: If appropriate, suggestions for further CITES activities concerning the management and
conservation of sea cucumbers in the families Holothuriidae and Stichopodidae, including
geographical and species priorities
“No additional listings” scenario:
1. CITES Parties should endorse the findings of the FAO ASCAM workshop.
2. CITES Authorities should draw the attention of their national fisheries agencies to the importance of
sea cucumber fisheries and the vulnerability of particular species in international trade. This could
include the need for:
a.
b.
c.
d.
Development of national fishery management plans or fishery regulations
Minimization of sea cucumber bycatch in other fisheries
National or provincial monitoring programs for sea cucumbers of commercial importance
Development of aquaculture and restocking programs, as appropriate
3. CITES Parties should encourage the regional cooperative management of commercially important sea
cucumber species, including the formation of appropriate Regional Fishery Management Organizations
(RFMO’s).
4. CITES Parties should encourage their national fisheries agencies to collaborate in the international
development of standardized population surveys and trade monitoring protocols.
5. CITES Parties should raise awareness of sea cucumber conservation problems in other Conventions
and agreements.
6. CITES Parties involved in the international trade of sea cucumbers should collaborate in the development
of universal marking and labeling schemes for specimens.
“Listing” scenario:
1. Appendix-III listing of Isostichopus fuscus by additional range States.
2. Appendix-III listing of additional sea cucumber species where necessary to complement national laws,
regulations, and management plans
31
3. Appendix II
a. Parties should propose all sea cucumber species currently in commercial trade for inclusion in
Appendix II (c. 30-45 spp. in Holothuriidae and Stichopodidae)
b. Parties should propose limited number of commercially important species in Appendix II and
monitor effectiveness
c. Parties should propose both families Stichopodidae and Holothuriidae under Article II 2(a)
and 2(b) (attach annex of all species in these families, noting range states)
4. Adopt measures and decisions noted above in the “non-listing” scenario
Output 3: A list of measures that range States should consider in case species of sea cucumbers
are included in Appendix II or III, indicating their feasibility, implications for stake holders,
practical recommendations for their implementation, and an evaluation of their costs and benefits.
Appendix III measures:
1. Pre-existing laws, regulations, or management measures that directly affect the international
trade in a given species from a given range State.
2. Establishment of a permit issuance system, in coordination with relevant national agencies
3. Consultation as per Res. Conf. 9.25 (rev).
4. Knowledge of species in trade, and forms in which they are traded.
5. Labeling and identification of products in trade.
Appendix-II measures:
1. All measures above, as per Appendix III listing.
2. Nature of export levels: ensure non-detrimental trade.
3. Monitor export levels to ensure species is sustainably harvested and in keeping with its role in
the ecosystem.
4. Law enforcement training.
Additional measures to facilitate Appendix-II listing:
1. Feasibility analysis for labeling
2. Identification tools/practical guides and forensic techniques
3. Technical assistance for: population survey methods, quota setting, cooperative management
4. Training and consultation on non-detriment findings
5. Public outreach to stakeholders, decision-makers, NGOs
6. Interagency collaboration between CITES authorities, law enforcement agencies, fisheries
agencies, NGOs
7. Call for assistance from other Parties
8. Collaboration with traders, fishers, and others for pragmatic implementation
32
Sea Cucumber Biology, Taxonomy,
Distribution and Conservation Status
Chantal Conand
Emeritus Professor, University of La Réunion, France
1. Basic information on the biology, taxonomy and distribution of sea cucumbers in the families
Holothuridae and Stichopodidae
1.1 Basic information on sea cucumbers
Holothurians have a long history of consumption by oriental populations, mostly chinese and japanese (Conand
1990). The most important sea cucumber product is the dried body wall which is marketed as beche-de-mer
(trepang or hai-som). In some countries medicines are produced, for example “gamat oil” in Malaysia (Baine
& Choo Poh Sze 1999). Holothurians represent one of the five extant classes of the phylum Echinodermata.
Dating back to 460 million years, they are characterized by their lack of segmentation, an endoskeleton of
calcareous ossicles and a large coelome with complex chambering giving the ambulacral or water-vascular
system where respiration, locomotion and sensory function are combined. The body symmetry is typically
pentaradial with a secondary bilateral symmetry. The alimentary canal is complete, the nervous system is not
centralized and the reproductive system is simple (Hyman 1955; Boolootian 1966).
They share a typical morphology, with a soft, cylindrical body, elongated from mouth to anus. They lie on the
sea floor, on the trivium the three ambulacral zones (ABE of the Carpenter system). They feed using buccal
tentacles which morphology varies according to the systematic of the orders within the class.
There are present in all regions of the ocean, from intertidal to deep ocean and from polar to tropical. There are
around 1500 species, new species being described each year with an increase of interest on the group (Massin
et al. 1999; Massin et al. 2004, Samyn & Berghe 2000 ; Samyn et al 2001 ;Uthicke et al 2004). The six
orders of this class are Dendrochirotida, Dactylochirotida, Aspidochirotida, Elasopodida, Apodida and
Molpadida. These are distinguished by the presence or absence of tube feet or podia (ambulacral system), the
shape of the mouth tentacles, and the presence or absence of oral retractor muscles, respiratory trees and
cuvierian tubules (see Conand 1990 for a general figure of the anatomy). Most commercial species belong to
the Aspidochirota (families Holothuridae and Stichopodidae) but a few Dendrochirota are showing some
interest and will be presented shortly.
1.2 Basic information on Aspidochirota (families Holothuridae and Stichopodidae) and Dendrochirota
Aspidochirota have many oral tentacles of peltate type used to feed on the bottom, as they are, with the
exception of the species Holothuria cinerascens detritus–feeders. On the trivium (which forms a creeping
ventral sole) the podia are arranged in three rows. On the bivium (dorsal surface) they occur in modified forms
as papillae. The body wall, the edible part, is composed of an epidermis and an underlying dermis of fibrous
connective tissue with spicules, pigments, coelomocytes. The spicules form the internal squeleton. These
microscopic calcareous components occur in a wide variety of forms used for the identification, which is there
fore not easy and requires special preparations, from different parts of the body (dorsal as well as ventral body
wall, tentacles and podia). The main forms are tiny rods, plates, rosettes, buttons, and different kinds of
tables.The anatomy is also characterized by the peripharyngeal calcareous ring formed of calcified plates,
differing between the species. They are attached to five longitudinal muscles. The digestive tract is long, comprising
a muscular pharynx, an oesophagus, and an intestine in three loops. The third loop going backwards terminates
into a large cloaca, opening through an anus sometimes ringed with anal teeth (example of Actinopyga species).
33
Two respiratory trees terminate in the cloaca. Cuvierian organs attached at the base of the respiratory trees,
are very sticky tubules. They can be expelled through the anus and are used as defensive organs. The reproductive
system consists of an unpaired genital gland composed of one or two tufts of tubules, terminating anteriorly by
a genital papilla. The main difference between the families Holothuridae and Stichopodidae is the anatomy of
the genital gland with one tuft in Holothuridae and two in Stichopodidae which also have special forms of
spicules.
Dendrochirota have an introvert, which is a collar of flexible tissue behind the tentacles pulled into the body
by retractor muscles; the tentacles are dendritic (branched) adapted to filter-feeding; the body wall is firm or
soft; the calcareous ring has developed posterior processes; the separate two gonad tufts characterize this
order.
2 . A short description of the main species in trade
Commercial sea-cucumber species are harvested according to the main geographical areas. In general, more
interest has been given to the biology of the species targeted in traditional fisheries than to more recent ones.
Despite the abundance and the large size of these animals and their importance in benthic communities, little
information is published on their population biology, compared with other living marine resources.
Tropical fisheries from the Indo-Pacific are multispecific, whereas temperate fisheries are generally monospecific.
Traditional tropical fisheries in the Western-Pacific and Indian Oceans produce dry product. Recently, some
countries have started exploitations on the Eastern-Pacific coasts. Temperate fisheries for fresh or frozen
product were long limited to the North-Western Pacific Ocean and there are now other countries interested on
different species.
Table 1 lists the commercial species according to the geographical regions, based on the FAO zones. When
possible the commercial interest from 1 (high value) to 3 (low value) is added in Table 1.
Many species are largely distributed in the tropical Indo-West Pacific. Recent careful observations are showing problems in taxonomy and several of the species listed could be different between these two oceans and
necessite revisions. This raises the important issue about modern taxonomy, based on cladistic studies and
genetics. This point deserves special attention, as the genetics of holothurians is a new field which should
develop, but it is money consuming.
2.1 Indo-West Pacific Regions
The genus are listed alphabetically for the Holothuridae first. Only the species with high and medium
commercial value will be presented briefly. More detailed descriptions and photographs are found in several
books or papers, as many countries have published inventories (Cherbonnier 1988 ; SPC 1994; Guille et
al.1986; Conand 1990; Conand 1998; Conand 1999; Richmond 1997; Samyn 2003). A programme granted
by WIOMSA, has started in the Western Indian Ocean and will bring new data on the main species, as well as
on the fisheries, in view of a better mamagement (Conand et al. 2006 ; www.wiomsa.org)
Genus Actinopyga
Actinopyga echinites is a medium sized species whose tegument varies in color, from light brown to orange.
It has numerous papillae dorsally and the anus is ringed by five calcareous teeth as for the other species of this
genus. The cuvierian tubules are rarely expelled. It is a common species on the shallow reef flats. Some traits
of its population biology (densities, reproduction, biometry) have been studied from New Caledonia and
Papua New Guinea.
34
Table 1 - Main commercial holothurian species. Commercial value code 1: high; 2: medium; 3: low. *
taxonomy to be revised. 1 H. whitmaei has been re-described ; H.nobilis distribution is now restricted to the IO ,
and H. whitmaei to the PWC and the W. Coast of Australia
Commercial
REGION
FAO code SPECIES
Family
value
Pacific Western Central- PWC 71+
Indian Ocean Eastern+ IOE 51+
IOE 57
Indian Ocean Eastern
Actinopyga echinites
Actinopyga lecanora
Actinopyga miliaris *
Actinopyga mauritiana
Actinopyga palauensis
Bohadschia atra
Bohadschia argus
Bohadschia marmorata *
Bohadschia subrubra
Bohadschia vitiensis *
Bohadschia similis
Holothuria arenicola
Holothuria cinerascens
Holothuria atra
Holothuria coluber
Holothuria edulis
Holothuria fuscogilva
Holothuria fuscopunctata
Holothuria leucospilota
Holothuria impatiens
Holothuria nobilis
Holothuria scabra
Holothuria whitmaei1
H. scabra versicolor
Pearsonothuria graefei
Stichopus chloronotus
Stichopus hermanni *
Stichopus horrens
Thelenota ananas
Thelenota anax
Thelenota rubralineata
Holothuridae
Holothuridae
Holothuridae
Holothuridae
Holothuridae
Holothuridae
Holothuridae
Holothuridae
Holothuridae
Holothuridae
Holothuridae
Holothuridae
Holothuridae
Holothuridae
Holothuridae
Holothuridae
Holothuridae
Holothuridae
Holothuridae
Holothuridae
Holothuridae
Holothuridae
Holothuridae
Holothuridae
Holothuridae
Stichopodidae
Stichopodidae
Stichopodidae
Stichopodidae
Stichopodidae
Stichopodidae
2
2
2
2
2
3
3
3
3
3
3
3
3
3
3
3
1
3
3
3
1
1
1
1
3
2
2
3
1
2
3
Pacific Eastern Central
Isostichopus fuscus
Actinopyga agassizi
Holothuria mexicana
Astichopus multifidus
Isostichopus badionotus
Apostichopus japonicus
Cucumaria japonica
Parastichopus parvimensis
Parastichopus californicus
Stichopus mollis
Athyonidium chilensis
Cucumaria frondosa
Stichopodidae
Holothuridae
Holothuridae
Stichopodidae
Stichopodidae
Stichopodidae
Cucumariidae
Stichopodidae
Stichopodidae
Stichopodidae
Cucumariidae
Cucumariidae
?
?
?
?
1
?
?
2?
?
?
?
PEC 77
AWC 31
Atlantic Western Central
PNW 61
Pacific Northwest
PNE 67
Pacific Northeast
Pacific Southwest
Pacific Southeast
Atlantic Northwest
PSW 81
PSE 87
ANW 21
35
Actinopyga lecanora is also a medium sized species whose tegument makes it look as a stone. It is relatively
rare in most sites and its biology has never been studied.
Actinopyga mauritiana is relatively larger. Its color is variable according to locations, from uniform brown to
brown with many white dots and small papillae. There could be different morphs in the Pacific and Indian
Ocean. Its habitat is restricted to the outer reef flats under the influence of the surf. Several studies have been
conducted on the population biology and particularly the sexual reproduction in New Caledonia, the Solomon
Islands, Guam.
Actinopyga miliaris and Actinopyga palauensis are two species with black tegument; they are of medium
size. Despite the high densities of some populations, there are no references on the populations of these
species.
Genus Bohadschia
The species are of low commercial value. Their cuvierian tubules are very abundant and sticky which makes
the processing difficult. They are collected in countries where the over-exploitation has diminished the other
commercial species.
Bohadschia atra is a large species found in Madagascar during an enquiry made with the collectors and
recently described (Massin et al. 1999). This shows that even large species, exploited in some places are
probably still undescribed.
Genus Holothuria
Holothuria fuscogilva is one of the two (or more) teatfish species, as the body wall presents lateral processes.
It has been described in 1980 by Cherbonnier, but the fishermen from the tropical Pacific used different names
for this white teatfish and H. nobilis the black teatfish. It is a large species (mean length 40 cm); its color is
variable from yellow to grey and often presents brown patches. It is a rather deep species found to 40 m depth,
but its densities are generally rather low. An example of scientific over-exploitation appeared due to the monthly
sampling in New Caledonia, where the catch per unit effort (CPUE) decreased strongly after a few months.
Holothuria nobilis the black teatfish is entirely black in the Pacific but the presence of white “teats” in the
Indian ocean has led to conduct a revision (Uthicke et al. 2004, Uthicke & Byrne pers. comm.). The population
biology of the black teatfish has been studied in several countries as this is one of the most exploited species.
It is smaller than the white teatfish (with a mean length of 37 cm in New Caledonia; Conand, 1989 ; Shiell &
Uthicke 2005). It is a typical reef flat species. It has not yet been studied in details in the Indian Ocean.
The two sandfish Holothuria scabra and Holothuria scabra versicolor (Conand 1986, 1999) have also
raised the interest recently. The genetics, as there is no difference in the spicules and calcareous ring and there
were some debate about the differences observed, will allow to distinguish them clearly (Rasolofonirina R.,
Vaïtilingon, D., Eeckhaut, I. & Jangoux M., 2005 and Purcell 2005).
Holothuria scabra is the sand fish, a species largely distributed and probably giving most of the tropical
captures for trepang. It shows some variability in color but most often it is entirely gray to dark. Its lateral
wrinkles are characteristic. It shows a preference for muddy sands and is often found in the vicinity of mangroves.
Many studies and a recent synthesis (Hamel et al. 2001) have been conducted on this important species,
which is used for stock enhancement or aquaculture in different places (India, the Solomon Islands, Madagascar,
Indonesia).
36
Holothuria scabra versicolor differs by a number of characters, by a larger mean size and a deeper habitat.
The dorsal tegument is highly variable from beige to black, with many specimens having black patches. The
papillae and tube feet are also more developed. Its seasonal reproductive cycle differs from H. scabra.
Many other Holothuria species have low value but are often collected when the high valued species are
becoming too rare.
Family Stichopodidae
The main Stichopodidae are less numerous they belong to two genera Stichopus and Thelenota. Their
characteristics are: a body square-shaped or trapezoidal in cross section, cuvierian organs always
absent, gonad in two tufts appended on each side of the dorsal mesentery and dominant spicules in branched
rods and C- and S-shaped rods.
Genus Stichopus
The genus Stichopus has a bivium covered by tubercules and papillae at least on its sides; the spicules develop
as tables, branched rods and C and S rods.
Stichopus chloronotus is a rather small species with a firm body of quadrangular shape; its green tegument
gives it the name of greenfish the ventral mouth is surrounded by a row of 20 stout tentacles. It lives in shallow
areas of the coral environment, with some populations attaining high densities. Some populations show a high
rate of asexual reproduction by fission. The genetic has been compared for Pacific and Indian ocean sites,
showing that asexual reproduction is an important feature in most populations, over a wide geographic range,
but also that the potential for widespread dispersal mediated by sexually produced larvae is large (Uthicke et
al. 2001; Conand et al.2002).
Stichopus hermanni (former S. variegatus) is a medium-sized species (mean about 35 cm) with a firm body
wall which disintegrates easily when collected as the other Stichopus. Its color yellow to greenish gives it its
name of curryfish. The bivium is covered by irregular conical warts arranged in 8 longitudinal rows, with
smaller papillae in between. It occurs in reefs and lagoons, in sea-grass beds, rubbles and muddy-sand bottoms.
As for most species the sexual reproduction takes place during the warm season. Its potential fecundity is low
and sexual maturity late, compared with the Holothuridae already studied, which makes it vulnerable to overexploitation.
Genus Thelenota
Thelenota ananas is a large species (maximum length 98 cm, mean 45 cm in New Caledonia) found in the reef
environment. Its bright orange-red color and the large papillae makes it very vulnerable to fishing. Its densities
are generally low. Its potential fecundity is low and sexual maturity late, compared with the Holothuridae
already studied, which makes it vulnerable to over-exploitation. Few studies have been made and the species
is now becoming rare.
Thelenota anax is even larger (mean length 60 cm) and rare, but is exploited in several countries. It lives on
the white coral sand of the reef slopes and is relatively deep. Nothing is known about its biology.
37
2.2 Other tropical Regions
Eastern Central Pacific
The fisheries are more recent than in the indo west pacific and target only a few species of large size and thick
tegument.
Isostichopus fuscus (Stichopodidae) is exploited in the Golf of California, Mexico, Ecuador mainland and
Galapagos islands. It is a conspicuous species (mean length 25 cm), living in the shallow waters (coral and
rocky bottoms). Many studies have been conducted on its reproductive biology (Herrero-Perezrul et al.
1999), on the population density and the fishery impact (Toral-Granda and Martinez in press). It is the only sea
cucumber which is listed on CITES Appendix III (Ecuador).
Western Central Atlantic
Small fisheries have recently started in Venezuela, Mexico and Cuba, based on Actinopyga agassizi, Holothuria
mexicana (Holothuridae family), Astichopus multifidus and Isostichopus badionotus (Stichopodidae family).
The description is after Hendler et al. 1995.
Actinopyga agassizi (Holothuridae) is a large species (maximum 35 cm in the Florida keys). Its body has
numerous wartlike papillae. The five anal teeth are conspicuous. The coloration is variable, most individuals are
mottled. It is a nocturnal species, living on coral reefs, rocky areas and sea-grass beds.
Holothuria mexicana (Holothuridae) is also a large species (max 50 cm). The body wall is rigid; there are a
few warts on the smooth upper surface; the colour is dark grey, brown or black in adults, but brownish yellow
in young specimens; the tube feet are brown with dark tips. It is encountered as solitary individuals on offshore
reefs.usually between 2-10 m depth. Its feeding activity is cyclical, peaking before midnight.
Astichopus multifidus (Stichopodidae) can reach 50 cm. Its bivium (dorsal side) is covered with numerous
papillae which give a hairy appearance. The body wall is soft with numerous spicules C-, O-, S-shaped and
also miliary grains. This species crawls slowly across the bottom and do not attach to the substrate. It is
characteristic of soft bottom, muddy or sandy, in and around seagrass beds.
Isostichopus badionotus (Stichopodidae) can reach 45 cm. It is distinguished by many dark darts on the
dorsal side and thick conical papillae on the lateral sides and three bands of crowded cylindrical tube feet. The
body wall is thick and rigid; its color varies largely. It is a common shallow -water species in the western
Atlantic, living on mud, sand or rocks, exposed when adult but the juveniles attach under the rubble. Its feeding
activity is cyclical, peaking before midnight.
2.3 Temperate Regions
Many articles published in the Beche-de-mer Information Bulletins from number 1 to 19 (SPC) have been
used to present the following species.
Northeast Pacific
Parastichopus californicus (Stichopodidae) is a common species from British Columbia to Mexico. Its
distribution goes from tide pools to 80 m. This large species (50 cm max) has a red to brown color. This
species, as Apostichopus japonicus can eviscerate seasonally in autumn. It can escape to sea star predation
38
by swimming movements. Its fishery has been monitored in Washington State (Bradbury 1997; Bradbury et
al. 1998).
Parastichopus parvimensis (Stichopodidae) has a geographical distribution.from California to Mexico
It is fished in Mexico. It is common on soft sediments and on rocks, from shallow waters to 60 m, with a strong
seasonal component, as they migrate into the deep in autumn. Spawning occurs in May-June; juveniles (0.56.0 cm) recruit to kelp holdfasts, from October to December; sub-adults (2-6 cm) are found under rocks and
adults (8-20 cm) on sand. Many specimens have no viscera from August to December, but it is not known if
this is from evisceration (as other species) or resorption (Muscat 1983).
Northwest Pacific
Apostichopus japonicus (Stichopodidae) is probably the first sea cucumber species to have been exploited
and studied by Chinese and Japanese in the Northwest Pacific (Choe 1963; Arakawa, 1990; Ito and Kitamura,
1998). The literature is therefore important. During many years of artisanal cultures have taken place. Recently
this species has given rise to an industrial large scale aquaculture in North East China (Chen Jiaxin and other
contributions in Lovatelli et al. in press), It would be of interest to compile all the data referring to this species
as it is the most studied temperate species
Cucumaria japonica (Dendrochitotida: Cucumariidae) is called Kinko in japanese. It is distributed from
northern Japan to Russia. Its body length is up to 20 cm and roundish; its color varies from grayish purple to
white. The young specimens inhabit shallow kelp habitat while the adults can aggregate on much deeper rocky
or muddy substrates. It is catched by trawling and is not used for dried product but rather for eating raw or
boiled. (Levin 1995).
Pacific Southwest and Southeast
Athyonidium chilensis (Dendrochitotida: Cucumariidae) is abundant in Peru and Chile (Ravest Presa 2000).
Little is known about this species.
Stichopus mollis ( Stichopodidae) is a common species, up to 36 cm in length, in shallow water of New
Zealand and parts of Australia. The knowledge is restricted to the seasonal evisceration and regeneration and
to the ecology and reproductive biology (Sewell 1990). Mladenov and Campbell (1998) presented a resource
evaluation in the Fiordland of New Zealand, from an experimental harvest; they pointed out that the potential
impact on the environment should be monitored.
Atlantic and other
Cucumaria frondosa (Dendrochitotida: Cucumariidae) is a cold water species of a large size (up to 50 cm).
It has been a by-catch of dredging before the project of a fishery as a pilot projet was set up (Hamel and
Mercier 1999). It is also a species which biology has been extensively studied (Hamel and Mercier 1996).
There are presently prospections in some countries for other species, as Holothuria forskali and Stichopus
regalis, but their commercial value is not known.
39
3. Summaries of the conservation status of sea cucumbers in the families Holothuridae and
Stichopodidae, indicating the main threats
3.1 Conservation status
The “Fishery System” of sea cucumbers is very complex, involving many levels from the fisherman to the
consumer and where different actors intervene. Table 2 shows the different levels for the sea cucumber and
there are interactions between the actors.(Conand 2001; Conand 2004). Therefore conservation has to be
well explained and understood at each level.
Table 2 - The different levels of the « Holothurian System » and the possible management
Fishery system
Management actions
1 Natural resources in commercial species
1a Research on biology and stock assessment
1b Hatcheries - production of juveniles
1c Sea ranching - mariculture
2 Fishermen catches collected by wading,
snorkelling, scuba diving
2a Respect of fishery legislations: size (bans of
juveniles), period, zones, national or
international (CITES?) legislations
2b Collection of standardized statistics
2c Education
3 Processing by fishermen or processors
3a Improving the quality during all phases of
processing
3b Storage, grading
3c Education
4 Fishery services national, then
international trade
4a
4b
4c
4d
5 Import and consumption
5 Information on market regulations and
preferences
Communication between the actors
Storage, grading
Standardized statistics
Access to information - legislations
The conservation status of sea cucumber mostly varies with the fishing region and therefore groups of species.
Both Bruckner et al. (2003) and Baine (2004) have distributed questionnaires in different countries and from
the results obtained presented the existing regulations for 20 to 30 countries, which are the main fishing places.
The following is based on their reviews, many contributions from the Beche-de-mer Information Bulletins
(SPC) and the ASCAM presentations (Lovatelli et al. 2004).
In temperate regions, the public awareness for conservation is generally stronger and new fisheries, when
they have started, have been followed, monitored and management decided. This is the case for the east and
west coast of Canada and USA. In Japan, the fishery for Apostichopus japonicus, as the other species are
only occasionally fished, is traditional (Choe 1963) and has also been managed using several measures as
Fishery laws, permits and a complex Fishery Adjustment System. These are presented, using the case study of
the Fishery Organization: Semposhi Fisheries Cooperative Association, Northern Hokkaido, by Akamine
(2004).
40
In tropical regions, the fisheries are on a small scale but have a great socio-economic importance for these
less developed countries. In the Indo west pacific, an exception is Australia where the fishery has a long history
but regulations have now been introduced for H. whitmaei and the results followed (Uthicke 2004). The main
fishing countries Indonesia and the Philippines are traditional but have no regulations. Some Pacific islands
(Fiji, Tonga) have introduced legal size limits (but are they controlled ?) or even a ban (Mozambique, Solomon
islands). In other countries, as Mexico, Galapagos, Cuba and Venezuela, the fisheries are more recent and the
attention has been raised on their management but despite this fact several conflicts or illegal fisheries have
occurred for these resources.
3.2 Threats
The main threat is over-exploitation by the fisheries for the processed dry product trepang (beche-de-mer in
the Pacific). The species with the high economic value (see Table 1) are more threatened, but given their
rarefaction other species with lower commercial value are now declining. The major consequence is the depletion
of sustainable breeding populations to permit natural replenishment of populations. In Malaysia other utilizations
are made from sea cucumber, for medicines, as “gamat oil” “gamat water”, balms after extraction from
Stichopodidae and pharmaceutical research for new products is also ongoing. (Baine and Choo 1999; Choo
et al. 2004). Another more general threat is the degradation of the habitats. This is more important in the
tropics and the overall decrease of the coral reefs worldwide is widely recognized and evaluated. The coralreef holothurians are particularly vulnerable.
4 . Knowledge gaps and research priorities in the area of biology, taxonomy and conservation status
4.1 Taxonomy
As already shown during the description of the main commercial species, it appears that the taxonomy is a very
difficult field in holothurians. There are only a few specialists, as this field has lost interest in the last decades.
But recently with the development of new methods of cladistic and more recently genetics, the systematic is
being revisited. It is no more based (as it used to be) on one or a few type specimens from one site. Therefore
questions about the large distribution of some species are asked. Research is urgently needed on the main
commercial species when differences have been noticed by observers. It could lead to the description of
different new species. The knowledge of the distinction of the species is a prerequisite to any conservation
based on individual species. This kind of conservation is necessary as it is the case for other marine resources.
Scientific teams from different zones of distribution of the targeted species and with capacities in classical
taxonomy, cladistic and genetics should be encouraged to collaborate. The more acute problems are in the
tropical Indian and west Pacific, as they the centers of biodiversity. As a priority, the commercial species of the
genera Actinopyga, Bohadschia, Holothuria, Stichopus certainly need further studies.
Another aspect, which has never been approached, is the identification of the processed specimens. It is
generally based on photographs, but some species look very much the same when they are dried. As the trade
is mostly done with the dried product, the identification at this stage has to be improved. It will be necessary to
check if enough spicules are kept on the body wall after processing.
4.2 Biology and ecology
Many parameters of the population biology of most commercial species are poorly or even not known. Very
often holothurians are considered to share the same characteristics and traits; this is entirely wrong and the
different species probably have different strategies; thus the findings on one species cannot be applied to
others. It should be clearly recognized that ecological traits differ markedly among species, thus a management
as a multi species fishery is strongly discouraged.
41
The recent ASCAM workshop organized by FAO in China (see Lovatelli et al. 2004 and many references to
the papers of the sessions) has allowed to develop recommendations agreed by the participants. From the
reports presented during this workshop on sea cucumber fisheries, management and aquaculture, it was clear
that sea cucumbers in most countries are suffering from heavy exploitation and population depletion. The main
recommendations deal with parameters for fishery models and have been used to prepare this contribution.
Research on growth rates, particularly in early stages must be gained from individual species, obtained in
laboratory and field studies. In addition, data from several locations need to be available in order to know if
patterns are general or location-specific. Information on mortality and longevity in the wild are also needed, to
allow sustainable catch rates to be estimated.
Research on larval ecology and recruitment processes of holothurians is also needed to develop fishery
models, and these processes will be widely variable in space and time. More studies should examine the
factors affecting the movement of sea cucumber larvae within the water column and factors influencing settlement. An understanding of larval movement and settlement processes will improve predictions on dispersal and
the likelihood of self-recruitment and natural replenishment of populations. Specifically, more information is
needed on the source and sink of recruits for local populations.
Stock assessment and stock delineation are also essential for conservation. Common methods of data
collection and presentation of results should be developed for commercially exploited species. Ideally, initial
stock surveys should be conducted before a fishery commences, in order to obtain information on virgin
biomass. Monitoring the recovery of stocks after fisheries have been closed should also be encouraged.
Research should focus on:
•
Habitat types (e.g. cover of sea grass or corals, sediment or substratum characteristics) should be
recorded for each survey unit (e.g. transect).
•
The size and spatial context of the populations need to be defined, in particular, the area surveyed and
the likely area occupied by the sub-population.
•
Stock delineation is important for managing stocks and understanding recruitment. Such information is
particularly relevant for restocking over broad spatial scales, due to likely adverse effects on genetic
diversity if genetically different stocks are mixed.
Maximum sustainable yields should be estimated for different types of sea cucumber fisheries, based on
surveys of stock size and estimates of recruitment, growth and natural mortality. In many cases, however, these
data may not be available. If this is the case, total allowable catch (TAC) should be conservative, assuming a
low % of virgin biomass can be taken, until monitoring of stocks, recruitment and catch data indicates that
catch rates could be increased. Moreover, TACs alone are not sufficient for the management because this tool
does not consider the size structure of existing stocks. A fishery could be made up of small animals, which are
harvested at the expense of egg production of the site.
Minimum stock size for viable breeding populations need to be maintained at a minimum threshold level to
ensure successful reproduction in the wild. This is because sea cucumbers use chemical cues to spawn and
need to be close to mates for fertilization of oocytes. Below such threshold densities of adults, populations will
fail to repopulate naturally. A disproportionate reduction of recruitment when densities of spawners are reduced
has been termed the “Allee” effect in the general ecological literature. Studies are needed to establish the
thresholds for minimum size of effective breeding populations.
42
The role of sea cucumbers in ecosystems has to be more studied. Data available indicate that removal of
these animals could lead to major changes to the ecosystem, such as decreased overall productivity. However,
to confirm this effect, large-scale experimental work in multiple areas with natural densities and over-fished
areas must be conducted.
4.3 Conservation Status
There is a general lack of information on appropriate management approaches and analytical tools. The fact
that over fishing and stock depletion is still occurring indicates that specific approaches are needed for
managing sea cucumber trading and fisheries. During the FAO ASCAM workshop it was recognized that a
critical need is to establish and implement management plans towards sustainability of adequate breeding
populations of all fished species (Lovatelli et al. 2004). Countries should also aim to develop management
prior to opening further fisheries. Management plans for sea cucumbers fisheries should be conservative
because stocks are vulnerable to over fishing. The most incipient threat is the depletion of sustainable breeding
populations to permit natural replenishment of populations. Different modes of management have been used
for sea cucumber fisheries, but few cases, both of failures and successes, have been documented. There is a
need for a review that summarizes case studies where management has worked and how participatory
management can be used.
Sea cucumber fishing is very important to the livelihoods of coastal communities, particularly artisanal and
small-scale fishers in developing countries. Therefore, socioeconomic issues in sea cucumber fisheries are
important, and should be recognized and incorporated in fishery management programs. In particular,
livelihood options should be made available to fishers if management regulation put restrictions on the fisheries,
such as bans on fishing.
Fisheries regulations should aim to protect ample breeding populations of each species. If the populations of
any species are fished below levels perceived to be minimal for breeding populations, then bans or moratoria
should be placed. For areas that have been closed to fishing by moratoria, the lifting of fishing bans should only
proceed after it is established that stocks are viable for reproduction and can sustain fishing.
The participants of ASCAM flagged a number of recommendations for fisheries managers, which should
be followed to prevent depletion of breeding stocks:
• The collection of sea cucumbers using compressed air (either SCUBA gear or hookah), or weighted
hooks should be restricted. Bans on using compressed air can protect deep stocks, but caution should
be given, because shallow stocks may be more important for spawning. In cases where scuba or
“hookah” diving is permitted, the divers need to be trained to avoid risk to life of the divers and adhere
to accepted OH&S guidelines, including the use of safe equipment.
• A “code of conduct” should be promoted for responsible fishing practices. This would involve common
sense fishing practices such as not collecting under-sized sea cucumbers and preserving a proportion
of the populations to act as breeding stock.
• Habitats should be protected as well as the resource. Authorities should endeavor to protect the
ecosystems in which sea cucumbers live and, conversely, recognize the important role that sea cucumbers
play in ecosystem processes. Where sea cucumber habitats have been damaged, rehabilitation should
be considered.
43
• Attention should be given to evaluating the occurrence and significance of sea cucumbers as by-catch
in trawl nets and dredges. These indiscriminant fishing methods can have impact populations and
habitat. By-catch of sea cucumbers in other fisheries needs to be both researched and documented.
Socio-economic and legislation. Public awareness of sea cucumber fisheries should be raised at a range of
levels, to highlight their importance and vulnerability to over fishing. Networking and cooperation among
researchers and fishery workers should be promoted. This could be by forming associations for processors
and traders, researchers, fishery managers and farmers. Additionally, newsgroups via email or internet would
be valuable for exchange of information.
Legislation should involve the following:
• Participation of stakeholders (including fishers, processors, policy makers, managers, exporters) in
forming management plans
• Authority divested at local/customary level, in certain circumstances (e.g. Melanesian artisanal fisheries
with customary tenure)
• Enforcement to ensure protection of sea cucumbers and their habitats
Scientists should test the effectiveness of Marine Protected Areas (MPAs) or No-Take Zones and methods
of management have not been documented. There is a need for a review that summarizes case studies where
management has worked and how participatory management can be used.
Knowledge on the effectiveness of MPAs (especially No-Take Zones) and comparison of a range of
management methods (such as broad fishery closure) should be collated. Research should also be encouraged
to determine the appropriate sizes, numbers and spatial design of MPAs. This could also include a review of
existing literature and case studies on MPAs.
Restocking is generally only a last resort if other management measures to recover a depleted fishery have
failed. Good management to preserve breeding populations should be the first solution, because there are risks
of changing genetic diversity of existing stocks when juveniles are released for restocking or stock
enhancement(Purcell, 2005).
Several recommendations from the Ascam workshop for restocking are:
• Studies needed about economic viability and returns from restocking programs in which hatcheryproduced juveniles are released into the wild.
• The value and significance of restocking to ecosystem functioning and long-term repopulation needs to
be included in cost-benefit analyses.
• Release of hatchery-produced juveniles should only be conducted at sites with the same genetic stock
as the broodstock used for production. Translocation of animals into foreign grounds should be
prohibited.
• Spawners (both male and female) must be chosen in sufficient numbers to warrant genetic diversity and
gene frequencies in the offspring similar to that in the receiving areas.
• Transfer of disease, parasites and introduced species from restocking needs care. Transfer protocols
and disease checks need to be developed to ensure healthy juveniles are used for restocking.
44
• The carrying capacity of the habitat (in terms of both number and biomass) should be evaluated before
restocking.
• Methods on the best strategies for releasing juveniles should be well determined prior to restocking.
Recent progress in aquaculture were presented at ASCAM (Lovatelli et al. 2004; SPC Beche de Mer
Bulletin 2004). The importance of this sector in northern China has been demonstrated by several participants
and will certainly influence the international trade. It will be necessary to follow its development and impacts.
Several programmes have started to cultivate H. scabra in the Indo-Pacific, as WorldFish in New Caledonia
(Purcell 2005) and Madagascar (Rasolofonirina & Jangoux 2004). Several recommendations from the Ascam
workshop are:
•
•
•
•
•
Publication of a manual or guide on sea cucumber aquaculture.
Enhancement of international exchanges.
Fundamental biological research including a better knowledge of the diseases and parasites.
Hatchery techniques.
Farming/sea ranching.
One of the concerns is the potential effect commercial-size aquaculture facilities on the environment. As the
industry develops, the benefit and usefulness of farming and sea ranching in different environments and
countries should be addressed and weighed against the cultural and environmental costs. Ultimately, guidelines
for ethics and conservation measures should be developed and promoted.
If international interventions (e.g. IUCN/CITES) are used to assist in the conservation and management
of sea cucumbers, caution should be placed on intervening or regulating trade for all regions due to differences
in the socio-economical situation of fishermen and the status of sea cucumbers habitats and environment.
5 - Information on key-reference materials and standard literature for sea cucumbers.
The SPC Beche-de-mer Informations Bulletins regularly published as issues (SPC) and immediately put on the
web http://www.spc.int/coastfish/news/BDM/23/index.htm are key-reference materials and http://
www.spc.int/coastfish/news/search_bdm.asp to search into the data base. They include original contributions
and abstracts of the recent litterature on holothurians. The Bulletin « Echinoderms Newsletter » on the web
http://www.nmnh.si.edu/iz/echinoderm also include useful informations. The International Echinoderm
Conference takes place every three year. Numerous presentations concern sea cucumbers. The Proceedings
are in books published previously by Balkema, now by Swets and Zeilinger, The Netherlands. (see Mooi &
Telford 1998; Barker 2001). In different countries inventories have been published (Cherbonier 1988; Guille
et al. 1986; Schoppe 2000) and manuals for processing sea-cucumbers intended for fishermen and trade, in
simple terms and local languages (T. & Nebelsick J. 2004).
Akamine J. 2004. Historical overview on holothurian exploitation, utilization and trade in Japan. In A. Lovatelli,
C. Conand, S. Purcell, S. Uthicke, J.-F. Hamel & A. Mercier, eds. Advances in sea cucumber aquaculture
and management. FAO, Rome. Fisheries Technical Paper No. 463, 425 pp.
Alfonso, I Ma. del Pilar Frías, L. Aleaga and C. R. Alonso. 2004. Current status of the sea cucumber fishery in
the south eastern region of Cuba. In A. Lovatelli, C. Conand, S. Purcell, S. Uthicke, J.-F. Hamel & A.
Mercier, eds. Advances in sea cucumber aquaculture and management. FAO, Rome. Fisheries Technical
Paper No. 463, 425 pp.
Altamirano M.H. and Toral-Granda M. V 2004. The application of the adaptive principle to the management and
conservation of Stichopus fuscus in the Galápagos islands, Ecuador In A. Lovatelli, C. Conand, S. Purcell, S.
Uthicke, J.-F. Hamel & A. Mercier, eds. Advances in sea cucumber aquaculture and management. FAO,
Rome. Fisheries Technical Paper No. 463, 425 pp.
45
Arakawa K.Y., 1990 - A handbook on the japanese sea cucumber : its biology, propagation and utilisation. Midori
Dhabo (ed.), Tokyo, Japan (en japonais).
Aumeeruddy R. and Rondolph Payet R. 2004. Management of the Seychelles sea cucumber fishery: status and
prospects. In A. Lovatelli, C. Conand, S. Purcell, S. Uthicke, J.-F. Hamel & A. Mercier, eds. Advances in
sea cucumber aquaculture and management. FAO, Rome. Fisheries Technical Paper No. 463, 425 pp.
Aumeeruddy R. & Skewes T. 2005. Resource assessment of the holothurian populations in the Seychelles S.P.C.
Bêche-de-mer Information Bull. 21: 19-21.
Aumeeruddy R, Skewes T, Dorizo J, Cedras M, Carocci F. & Coeur de Lion F 2005. Resource assessment
of the holothurian populations of the Seychelles. 4th Wiomsa Scientific Symposium (abstract)
Baine M. 2004. From the sea to the market place: an examination of the issues, problems and opportunities in
unravelling the complexities of sea cucumber fisheries and trade. In A. Lovatelli, C. Conand, S. Purcell, S.
Uthicke, J.-F. Hamel & A. Mercier, eds. Advances in sea cucumber aquaculture and management. FAO,
Rome. Fisheries Technical Paper No. 463, 425 pp.
Baine, M. & Choo Poh Sze 1999. Sea cucumber fishery and trade in Malaysia. In The conservation of sea
cucumbers in Malaysia: Their ecology, taxonomy and trade. Baine (ed.): 49-63.
Baine, M. (ed.) 1999. The conservation of sea cucumbers in Malaysia: Their ecology, taxonomy and trade: 82p.
Barker M. (ed.) 2001. Echinoderms 2000. Proceedings of the 10th Int. Echinoderm Conference. Balkema, Swets
and Zeilinger The Netherlands, 590 pp.
Boolootian R.A., 1966 - Physiology of Echinodermata. Wiley (ed) Interscience, New York : 822 p.
Bradbury A. 1997. Fishery in Washington State. Beche-De-Mer Information Bulletin 9: 11.
Bradbury A., Palsson W.A. and Pacunski R.E. 1998. Stock assessment of the sea cucumber Parastichopus
californicus in Washington. In Echinoderms San Francisco, Mooi & Telford (eds). Balkema : 441-446
Bruckner A.W. 2002. Correspondence. Beche-De-Mer Information Bulletin 17: 39.
Bruckner A. 2005. The recent status of sea cucumber fisheries in the continental United States of America. SPC
Beche-de-mer Information Bulletin 22
Bruckner A.W., Johnson K.A. and Field J.D. 2003. Conservation strategies for sea cucumbers: can a CITES
Appendix II listing promote international trade? Beche-de-mer Information Bulletin 18 : 24-33
Bunce, L., Townsley P., Pomeroy, R., and Pollnac, R. 2000. Socioeconomics manual for coral reef
management. Australian Institute of Marine Science, p. 92-168.
Cherbonnier G. 1988 Echinodermes : Holothuries. In : Faune de Madagascar, 70, ORSTOM, Paris: 292 p
Cherbonnier G., 1980 - Holothuries de Nouvelle-Calédonie. Bull. Mus. natl. Hist. nat., Paris, 4e ser., 2(3) : 615667.
Choe S., 1963 - Biology of the Japanese Common Sea Cucumber Stichopus japonicus, Selenka. Pusan National
University, Pusan : 226 p. (en japonais).
Choo P-S. 2004. Fisheries, Trade and Utilization of Sea Cucumbers in Malaysia. In A. Lovatelli, C. Conand, S.
Purcell, S. Uthicke, J.-F. Hamel & A. Mercier, eds. Advances in sea cucumber aquaculture and
management. FAO, Rome. Technical Paper No. 463, 425 pp.
Clark, A. M. & F. W. E. Rowe 1971. Monograph of the Shallow-Water Indo-West Pacific Echinoderms.
Bath,England, Pitman Press.
Conand, C. 1989. Les holothuries aspidochirotes du lagon de Nouvelle-Calédonie : Biologie, Ecologie et exploitation.
Etudes et thèses, ORSTOM: 393 p.
Conand, C. 1990. The fishery resources of Pacific island countries. Part 2: Holothurians. F.A.O. Fisheries Technical
Paper, Rome, No. 272 (2): 143 pp.
Conand C. 1993. Reproductive biology of the characteristic holothurians from the major communities of the
New Caledonia lagoon. Mar.Biol. 116 : 439-450.
Conand C., 1996. Asexual reproduction by fission in Holothuria atra : Variability of some parameters in populations
from the tropical Indo-Pacific. Oceanologica Acta 19, 3: 209-216.
Conand, C. 1998. Overexploitation in the present sea cucumber fisheries and perspectives in mariculture. In:
Echinoderms: San Francisco (eds. R. Mooi and M. Telford): 449-454.
Conand C., 1998 - Holothurians. in FAO species identification guide. The marine living resources of the
Western Central Pacific. vol 2 cephalopods, crustaceans, holothurians and sharks, K Carpenter & V. Niem
eds. : 1157-1190.
46
Conand C, 1999. Manuel de qualité des holothuries commerciales du Sud-Ouest de l’Océan Indien. PRE/COI:
39p.
Conand C., 2001. Overview of sea cucumbers fisheries over the last decade - what possibilities for a durable
management ? : 339-344, in: Echinoderm 2000, Barker M. (scientific ed.), Balkema, Swets & Zeitlinger:, The
Netherlands.
Conand C., 2004. Present status of world sea cucumber resources and utilisation: An international overview. In
A. Lovatelli, C. Conand, S. Purcell, S. Uthicke, J.-F. Hamel & A. Mercier, eds. Advances in sea cucumber
aquaculture and management. FAO, Rome. Technical Paper No. 463, 425 pp.
Conand C. 2004b. Convention on International Trade in Endangered Species of Wild Fauna and Flora
(CITES):conservation and trade in sea cucumbers. S.P.C. Bêche-de-mer Information Bull., 20: 3-5.
Conand C 2004c. Suivi de la population scissipare de Holothuria atra d’un récif frangeant de l’Ile de La
Reunion (Ocean indien) S.P. C. Bêche-de-mer Information Bull 20: 22-25
Conand, C. and Byrne, M. 1993. A review of recent developments in the world sea cucumber fisheries. Marine
Fisheries Review 55: 1-13.
Conand, C., De San, M., Refeno, G., Razafintseheno, G., Mara, E. and Andriajatovo, S. 1998. Sustainable
management of the sea cucumber fishery in Madagascar. Beche-de-mer Information Bulletin 10: 7-9.
Conand C, Uthicke S. & Hoareau T. 2002. Sexual and asexual reproduction of the holothurian Stichopus
chloronotus (Echinodermata) : a comparison between La Réunion (Indian Ocean) and east Australia (Pacific
Ocean). Invert. Reprod. Develop. 41 (1-3): 235-242.
Conand C. & Mangion P. 2002. Sea cucumbers on La Reunion Island fringing reefs: diversity, distribution,
abundance and structure of the populations. S.P.C. Bêche-de-mer Information Bull 17 : 27-32
Conand C., Dinhut V., Quod J-P & R. Rolland 2005. Eléments pour l’inventaire des holothuries de Mayotte, sudouest océan indien S.P.C. Bêche-de-mer Information Bulletin, 22 :19-22
Conand C., Muthiga N., Aumeeruddy R., De La Torre Castro M, Frouin P, Mgaya Y, Mirault E, Ochiewo J.,
Rasolofonirina R. 2006. A three year regional project on sea cucumbers in the south-western indian ocean :
national and regional analyses to improve management S.P.C. Bêche-de-mer Information Bull., 23:11-15.
De la Torre-Castro M. & Rönnback P. 2004. Links between humans and sea grasses- an example from
tropical East Africa. Ocean and coastal Management 47: 361-387
FAO 1994 to 2003. Fishery statistics 1992 to 2001. Vol. 68: Catches and landings. FAO Rome.
Ferdouse F. 1999. Beche-de-mer markets and utilisation.. Beche-de-mer Information Bulletin 11: 3 – 8.
Ferdouse F. 2004. World markets and trade flows of sea cucumber/beche-de-mer. In A. Lovatelli, C. Conand, S.
Purcell, S. Uthicke, J.-F. Hamel & A. Mercier, eds. Advances in sea cucumber aquaculture and
management. FAO, Rome. Technical Paper No. 463, 425 pp.
Gamboa R., Gomez L., Nievales M.F., Bangi H.G. Juino-Menez M.A. 2004. The status of sea cucumber fisheries
and mariculture in the Philippines. In A. Lovatelli, C. Conand, S. Purcell, S. Uthicke, J.-F. Hamel & A.
Mercier, eds. Advances in sea cucumber aquaculture and management. FAO, Rome. Technical Paper
No. 463, 425 pp.
Grandcourt E.M. & Cesar H.S. 2003. The bio-economic impact of mass coral mortality on the coastal reef
fisheriesof the Seychelles. Fisheries Research 60: 539-550.
Guille A.., Laboute P. & Menou J.L., 1986 - Guide des étoiles de mer, oursins et autres echinodermes du lagon de
Nouvelle-Calédonie. ORSTOM (ed), Coll. Faune tropicale, Paris, 25 : 238 p.
Hamel J.F. and Mercier A. 1996 - Early development, settlement, growth, and spacial distribution of the sea
cucumber Cucumaria frondosa (Echinodermata : Holothuroidea). Can. J. Fish. Aquat. Sci. 53: 0-00
Hamel J.F. and Mercier A. 1999. Recent developments in the commercialisation of the northern sea cucumber
Cucumaria frondosa. Beche-de-mer Information Bulletin 11: 21-22
Hamel J-F, Conand C., Pawson D. L., & A. Mercier, 2001 - Biology of the sea cucumber Holothuria scabra
(holothuroidea: echinodermata) and its exploitation as beche-de-mer. Advances in Mar. Biol., 41 : 129-223
Hendler G., Miller J E., Pawson D. and Kier P. 1995 - Sea stars, sea urchins and allies Echinoderms of Florida and
the caribbean. Smithsonian Institution Press, 390 pp
Heinzeller T. & Nebelsick J. (eds) 2004. Echinoderms : Mundchen. Balkema, London ; 633 pp
Herrero-Perezrul D., Reyes-Bonilla H., Garcia-Dominguez and Cintra-Buenrostro C. 1999 Reproduction and
growth of Isostichopus fuscus in the southern gulf of California, Mexico. Mar. Biol. 135: 521-532.
47
Horsfall I.M. 1998. Sea cucumbers of Tanzania. Miombo 18: 4-5.
Humphreys, W. F. 1981. “The Echinoderms of Kenya’s marine parks and adjacent regions.” Zoologische
Documentatie 19:1-37.
Hyman L.H., 1955 - The Invertebrates : Echinodermata. In : The Coelomate bilateria, Mc. Graw Hill (ed), vol.
IV : 1-763.
Ibarra A. A. and Soberon G. R. 2002. Economic reasons, ecological actions and social consequences in the
Mexican sea cucumber fishery. Beche-de-mer Information Bulletin 17:33-36
Ito S. & Kitamura H. (1998) Technical development in seed production of the sea cucumber Stichopus japonicus.
Beche-de-mer Information Bulletin 10: 24-28
Jangoux, M., Rasolofonirina, R., Vaïtilingon, D., Ouin, J.M., Seghers, G., Mara, E., & Conand, C. 2001. A sea
cucumber hatchery and mariculture project in Toliara, Madagascar. SPC Bêche-de-mer Bull, 14: 2-5..
Jennings S. & Polunin N.V.C. 1996. Impacts of fishing on tropical reef ecosystems. Ambio 25(1) 44-49
Jennings S. & Kaiser M.J. 1998. The effects of fishing on marine ecosystems. Adv. Mar. Biol. 34, 203-352.
Jiddawi N.S. & Öhman M.C. 2003. Marine fisheries in Tanzania. Ambio 31: 518-27.
Jiaxin C. 2003. Overview of sea cucumber farming and sea ranching practices in China. Beche-de-mer Information
Bulletin 18: 18-23
Jiaxin C. 2004. Present status and prospects of sea cucumber industry in China. In A. Lovatelli, C. Conand, S.
Purcell, S. Uthicke, J.-F. Hamel & A. Mercier, eds. Advances in sea cucumber aquaculture and
management. FAO, Rome. Technical Paper No. 463, 425 pp.
Lawrence, A.J, Ahmed, M., Hanafy, M, Gabr, H and Ibrahim, A. 2004. Status of the Sea Cucumber Fishery in the
Red Sea – The Egyptian Experience. In A. Lovatelli, C. Conand, S. Purcell, S. Uthicke, J.-F. Hamel & A.
Mercier, eds. Advances in sea cucumber aquaculture and management. FAO, Rome.
Levin V. 1995. Japanese sea cucumber Cucumaria japonica in the far eastern seas of Russia. Beche-de-mer
Information Bulletin 7: 18-19.
Lovatelli, C. Conand, S. Purcell, S. Uthicke, J.-F. Hamel & A. Mercier, (eds). 2004 Advances in sea cucumber
aquaculture and management. FAO, Rome. Technical Paper No. 463, 425 pp.
Mangion P., Taddei D., Frouin P. & Conand C. 2004. Feeding rate and impact of sediment reworking by
twodeposit feeders Holothuria leucospilota and Holothuria atra on a fringing reef (Reunion Island,
Indian), Echinoderms: München - Heinzeller & Nebelsick (eds), Taylor & Francis, London: 311-317
Mara, E., Rasolofonirina, R., Rabesandratana, H., Rakotoarinivo, W., Ravelo, I. & Conand, C. (1998). Etude de
la pêcherie aux holothuries et propositions de mesures d’aménagement dans le Sud-ouest de Madagascar.
Report IH.SM/ONE/BM, Toliara. 40pp.
Marshall NT, Milledge AH & Afonso PS 2001. Trade Review: Stormy Seas for Marine Invertebrate: trade in
Sea Cucumbers, Seashells and Lobsters in Kenya, Tanzania and Mozambique. WWF IUCN (1-70)
Massin C, Rasolofonirina R., Conand C. & Samyn Y., 1999 - A new species of Bohadschia (Echinodermata,
Holothuroidea) from the Western Indian Ocean with a redescription of Bohadschia subrubra. Bull inst.
Royal Sciences Belgique 69 : 151-160
Massin C. , Samyn Y., Thandar AS in press. The genus Labidodemas (Holothuroidea: Aspidochirota) revisited
with description of three new species and with re-positioning of Holothuria maccullochi Deichmann 1958.
Journal of Natural History.
Martinez P.C. 2001. The Galapagos sea cucumber fishery: a risk or an opportunity for conservation? Beche-deMer Information Bulletin 14: 22-23.
McClanahan T.R. & N.A. Muthiga. 1992. Comparative sampling of epibenthic subtidal gastropods. Journal of
Experimental Marine Biology and Ecology 164: 87-101.
McClanahan T.R. & L. Pet-Soede 2000. Kenyan coral reef fish, fisheries and economics - trends and status
afterthe 1998 coral mortality. S. Westmacott, H. Cesar and L. Pet-Soede. Amsterdam, Institute of
Environmental Studies, Free University: 79-100.
McClanahan T.R. & C.R. Sheppard (Eds). 2000. Coral Reefs of the Indian Ocean: Their Ecology and
Conservation. New York, Oxford University Press.
McClanahan, T.R. & J. Maina. 2002. Effects of the 1998 coral mortality event on Kenyan coral reefs and
fisheries. Ambio 31(7-8): 543-550.
48
Mladenov P. & Campbell A. 1998. Resource evaluation of the sea cucumber Stichopus mollis, in the
environmentally sensitive Fiordland region of New Zealand. Echinoderms: San Francisco, Mooi & Telford eds,
Balkema, Rotterdam : 481-487
Mmbaga T.K.and Mgaya Y.D. 2004. Studies on sea cucumber in Tanzania and the gaps towards resource
inventory and management. In A. Lovatelli, C. Conand, S. Purcell, S. Uthicke, J.-F. Hamel & A. Mercier,
eds. Advances in sea cucumber aquaculture and management. FAO, Rome. Technical Paper No. 463, 425
pp.
Mooi R. and Telford M. (eds) 1998. Echinoderms: San Francisco. Proceedings of the 9th Int.Echinoderm
Conference. Balkema, Rotterdam, 923 pp.
Muscat A. 1983. Population dynamics and the effects on the infauna of the deposit feeding holothurian Parastichopus
parvimensis (Clark). Ph. D. Thesis, Univ. of Southern California : 328 p.
Muthiga, N.A. & Ndirangu, S. 2000. Village based larviculture and stock enhancement of sea cucumbers
(Echinodermata: Holothuroidea) on the Kenyan coast pp 66. Final Technical Report, Biodiversity Support
Fund.
Muthiga, N.A. 2005. The reproductive biology of a new species of sea cucumber, Holothuria (Mertensiothuria)
arenacava in a Kenyan marine protected area: the possible role of light and temperature on gametogenesis
and spawning. Marine Biology (on line)
Polon P. 2004. The Papua New Guinea national Beche-de-mer fishery management plan. In A. Lovatelli, C. Conand,
S. Purcell, S. Uthicke, J.-F. Hamel & A. Mercier, eds. Advances in sea cucumber aquaculture and
management. FAO, Rome. Technical Paper No. 463, 425 pp.
Pouget A. 2005. Abundance and distribution of holothurians on the fringing reef flats of Mayotte. S.P.C.
Bêche-de-mer Information Bull. 21:22-25
Purcell S.W. 2004. Criteria for release strategies and evaluating the restocking of sea cucumbers. In A. Lovatelli,
C. Conand, S. Purcell, S. Uthicke, J.-F. Hamel & A. Mercier, eds. Advances in sea cucumber aquaculture
and management. FAO, Rome.Technical Paper No. 463, 425 pp.
Purcell S.W. 2005. Developing technologies for restocking sandfish:Update on the WorldFish–SPC project in
New Caledonia. SPC Beche-de-mer Information Bulletin #22 : 30-33.
Ramofafia C., Foyle T.P. & Bell J.D., 1997. Growth of juvenile Actinopyga mauritiana (Holothuroidea) in
captivity. Aquaculture 152: 119-128
Ramofafia C., Lane I. and Oengpepa C. 2004. Customary marine tenure in Solomon islands: a shifting paradigm
for management of sea cucumbers in artisanal fisheries. In A. Lovatelli, C. Conand, S. Purcell, S. Uthicke, J.F. Hamel & A. Mercier, eds. Advances in sea cucumber aquaculture and management. FAO, Rome.
Rasolofonirina R., Vaïtilingon, D., Eeckhaut, I. & Jangoux M., 2005. Reproductive Cycle of Edible Echinoderms
from the SouthWestern Indian Ocean II: The sandfish Holothuria scabra (Jaëger, 1833). Western Indian
Ocean J. Mar. Sci. Vol. 4, No. 1, pp. 61–75 (on line on www.wiomsa.org).
Rasolofonirina R 2005. Reproduction et développement de l’holothurie Holothuria scabra à Madagascar
(Holothuroidea : Echinodermata). PhD, ULB, Bruxelles. Summary in Beche-de-mer Info. Bull. 21 : 38-39
Rasolofonirina R. & Conand C.; 1998. Sea cucumber exploitation in the Toliara region of south-west Madagascar.
Beche-de-mer Information Bulletin 10:10–13.
Rasolofonirina R., Mara E. & Jangoux M. 2004. Sea cucumber fishery and mariculture in Madagascar: A
case study of Toliara, south-west of Madagascar :133-149 in Lovatelli, C. Conand, S. Purcell,S. Uthicke,
J-F.Hamel & A. Mercier (eds.) Advances in sea cucumber aquaculture and management. FAO Fisheries
Technical Paper No. 463, 425 pp
Ravest Presa C. 2000. Athyonidium chilensis Beche-de-mer Information Bulletin 13: 9.
Richmond M. 1997. A guide to the seashores of eastern Africa and the western indian ocean islands. SIDA ,
448 p
Rowe F. & Richmond M. 2004. A preliminary account of the shallow-water Echinoderms of Rodrigues,
Mauritius,western Indian Ocean. Journal of Natural History. 38 :3273-3314.
Rodriguez-Millet E. and Pauls S.M. 1998. Sea cucumber fisheries in Venezuela. In Echinoderms San
Francisco, Mooi & Telford (eds). Balkema : 513-516
49
Samyn Y, & Berghe V.E. 2000. Annotated checklist of the echinoderms from the Kiunga Marine National
Reserve,Kenya. Part 1: Echinoidea and Holothuroidea. Journal of East African Natural History 89: 1-36
Samyn Y., Massin C. & Muthiga N.A. 2001. A new species of Holothuria (Aspidochirotida, Holothuriidae)
fromKenya. Annals Sciences Zoologiques 285: 101-110
Samyn Y. 2003. Towards an understanding of the shallow-water holothuroid fauna (Echnodermata: holothuroidea)
of the western indian Ocean. PhD Thesis Vrije Universiteit Brussel : 384 pp.
Samyn Y., VandenSpiegel D. & C. Massin . 2005. Sea Cucumbers of the Comoros Archipelago. S.P.C. Bêchede-mer Information Bull., 22 :14-18
Schoppe S. 2000. Sea cucumber fishery in the Philippines. Beche-de-Mer Information Bulletin 13: 10-12.
Schroeter S.C., Reed D. C., Kushner D.J., Estes J.A. and Ono D.S. 2001. The use of marine reserves in
evaluating the dive fishery for the warty sea cucumber (Parastichopus parvimensis) in California, USA.
Can. J. Fish. Aquat. Sci. 58: 1773-1781.
Sewell M.A 1990. Aspects of the ecology of Stichopus mollis (Echinodermata: Holothuroidea) in north-eastern
New Zealand. New Zeal. J. Mar. Freshw. Res., 24: 97-103.
Shelley C.C. and Puig P. 2004. Management of trepang in the Northern Territory, Australia, and current research
to further improve understanding of the fishery. In A. Lovatelli, C. Conand, S. Purcell, S. Uthicke, J.-F. Hamel
& A. Mercier, eds. Advances in sea cucumber aquaculture and management. FAO, Rome. Technical
Paper No. 463, 425 pp.
Shiell G.R. 2004. Bêche-de-mer; the west australian perspective: the fishing history and aspects of the reproductive
biology and ecology of the black teat fish, Holothuria nobilis. In A. Lovatelli, C. Conand, S. Purcell, S.
Uthicke, J.-F. Hamel & A. Mercier, eds. Advances in sea cucumber aquaculture and management. FAO,
Rome. Technical Paper No. 463, 425 pp.
Shiell G. & Uthicke S. 2005 Reproduction of the commercial sea cucumber Holothuria whitmaei
[Holothuroidea: Aspidochirotida] in the Indian and Pacific Ocean regions of Australia. Mar Biol (on line)
Shiell G. 2004. Questionnaire on the field observation of juvenile sea cucumbers. S.P.C. Bêche-de-mer
InformationBull., 19 : 41
S.P.C 1990 to 2006. Beche-de-mer Information Bulletin 1 to 23. Secretariat of the Pacific Community
http://www.spc.int/coastfish/news/BDM/
S.P.C. 1994. Sea cucumbers and beche-de-mer of the Tropical Pacific. Secretariat of the Pacific Community.
Handbook 18, 51 pp.
Toral-Granda M.V. & Martínez P.C. 2004. Population density and fishery impacts on the sea cucumber (Stichopus
fuscus) in the Galápagos islands. In A. Lovatelli, C. Conand, S. Purcell, S. Uthicke, J.-F. Hamel & A.
Mercier, eds. Advances in sea cucumber aquaculture and management. FAO, Rome.Technical Paper No.
463, 425 pp.
Tuwo A. 2004. Status on sea cucumber fisheries and farming in Indonesia. In A. Lovatelli, C. Conand, S. Purcell,
S. Uthicke, J.-F. Hamel & A. Mercier, eds. Advances in sea cucumber aquaculture and management.
FAO, Rome.Technical Paper No. 463, 425 pp.
Uthicke S., C. Conand & J. A. H. Benzie 2001 - Population genetics of the fissiparous holothurians and Stichopus
chloronotus and Holothuria atra (Aspidochirotida): a comparison between Torres Strait and La Réunion
Mar. Biol. 139 : 257-265
Uthicke S. 2004. Over fishing of holothurians: lessons from the Great Barrier Reef. In A. Lovatelli, C. Conand,
S. Purcell, S. Uthicke, J.-F. Hamel & A. Mercier, eds. Advances in sea cucumber aquaculture and
management. FAO, Rome.Technical Paper No. 463, 425 pp.
Uthicke S. & Conand C. 2005a. Local examples of beche-de-mer overfishing: an initial summary and request
for information. Bêche-de-mer Information Bull., 21 : 9-14
Uthicke S. & Conand C. 2005b . Amplified fragment length polymorphism (AFLP) analysis indicates
importance of both asexual and sexual reproduction in the fissiparous holothurian Stichopus chloronotus
(Aspidochirotida) in the Indian and Pacific Ocean. Coral reefs, 24: 103–111
Uthicke S., O’Hara T. & Byrne M. 2004 b. Species composition and molecular phylogeny of the Indo-Pacific
teatfish (Echinodermata:Holothuroidea) bêche-de-mer Fishery. Marine and Freshwater Research. 55:1–12
50
Harvest and Trade; Utilization of Sea Cucumbers: Sea Cucumber Fisheries;
Current International Trade; Illegal, Unreported and Unregulated Trade;
Bycatch; Socio-Economic Characteristics of the Trade in Sea Cucumbers
Chantal Conand,
Emeritus Professor, University of La Réunion, France
Introduction
The "Holothurian Fishery System" presented earlier (Conand & Byrne 1993; Conand 1998, 2001 and 2004)
is a good model for all sea cucumber fisheries (Figure 1). The five levels of this system between the resource
on the sea floor and the plate of the consumer, are very important both for fishery evaluations and for durable
management (see also Table 2 in document 1 for this CITES workshop). At each level and between the levels,
different participants intervene.
Figure 1. The holothurian fishery, from the sea-bed to the consumer and the levels of collecting statistics
51
In most of the fisheries, the catch is processed into a dried product, called "Trepang" in the Indian ocean,
"Beche-de Mer" in the tropical pacific, "Hai-som" by Chinese and "Iriko" by Japanese (Conand 1990; Preston
1993). This processing is complex (see paragraph 5); the dehydratation is variable between holothurian species
and processors, but a mean decrease in weight is of about 90%. The studies and reports must therefore be
very careful in the unit used and many inaccuracies have resulted from not taking this point into account.
The recent meeting "Advances in Sea Cucumber Aquaculture and Management (ASCAM), organized by
FAO in China in October 2003 (Lovatelli et al. 2004) has gathered fifty experts from different parts of the
world and from China. The contributions have presented the recent status of many fisheries, the existing
management and the aquaculture advances. The participants have also made recommendations on these three
topics. The present document will take these new findings and ideas into account.
As presented in the document 1 for this CITES workshop, The SPC Beche-de-Mer Information Bulletins
contains many useful publications (http://www.spc.int/coastfish/news/BDM/).
1. General information on the current levels of harvest and trade in sea cucumbers, with wherever
possible: indications of recent trends in harvest and trade, main fisheries, main exporting and
importing countries, sources of sea cucumbers (i.e. wild or aquaculture), origins, trade routes, and
principal species in trade
1.1. Current levels and recent trends of harvest and trade in sea cucumbers and main fisheries
The fisheries can be presented according to the geographical area and the species harvested. Tropical fisheries
from the Indo-Pacific are multispecific, whereas temperate fisheries are generally monospecific. Traditional
tropical fisheries in the Western-Pacific and Indian Oceans produce dry product. Recently, some countries
have started exploitations on the Eastern-Pacific coasts. Temperate fisheries for fresh or frozen product were
long limited to the NorthWestern Pacific Ocean and there are now other countries interested. Fishery statistics
have been collected from several sources, including producer countries (catch and export statistics) and
international FAO data (annual yearbooks for catches, FAO 1992 to 2001). These data are synthesized for
the last decade to show where most products originate and which are the new trends. The gaps or inaccuracies
will be discussed to help formulate recommendations for a future better fishery knowledge and management.
Table 1 presents the data on the harvest of sea cucumbers, adapted from FAO Statistics by country and
corrected with the recent information obtained for several countries, during the ASCAM Workshop in
October 2004. This table is in two parts: 1) All the species excepted Apostichopus japonicus, as the data are
mainly for dry product; 2) Apostichopus japonicus data for Japan, Korea and China (partly) with data in
fresh weight. As the processed product is only 10% or less of the live sea cucumber weight, it is essential to
distinguish these categories.
In Table 1, the countries are presented alphabetically, but the FAO regions are precised. The data are given
for the last decade and its mean is calculated, which helps to follow the recent trends.
52
Table 1: Captures or beche-de-mer productions (t) by country and mean value for the decade (from
FAO data and other sources)
Country
Holothurioidea
dry weight
Chili
Cuba
Ecuador
Egypt
Fidji
Indonésie
Indonésie
Solomon
Kenya
Kiribati
Madagascar
Malaysia
Maldives
Mexico
Mozambique
New Caledonia
New Zealand
Palau
Papua New
Guinea
Spain
Philippines
Sri Lanka
Tanzania
Tonga
Canada
U.S.A.
U.S.A.
Vanuatu
Yemen
Total
holothuroidea
Apostichopus
japonicus
Japan
Repub Korea
China
Total
Apostichopus
FAO
region 1992 1993 1994
P SE
237
13
1995
4
1996
106
1997 1998
1999
115
1
30
P EC
29 12
12
12
12
IOW
P WC
447 191
400
835
850
IOE
269
P WC 3,130 2,364 3,130 2,562 2,800
P WC
715 720
700
700
750
IO W
277 14
41
55
15
PWC
IO W
423 450 1,800 1,800 1,800
P WC
...
...
...
...
...
IO W
119 72
66
94
145
PEC
IO W
0
0
0
6
54
P WC 1,090 777
798
480
493
P SW
0
0
0
4
1
P WC
2
2
2
2
6
12
790
338
2800
203
41
136
1800
…
318
7
565
0
7
15
P WC
600 650
600
640
650
M
4
P WC 3,679 3,109 1,497 2,062 2,123
IO W
65 65
92
100
100
IO W
535 980 1,591 1,460 1,644
P WC
...
...
...
...
86
PNE
0
0 1,505
0 1 288 ?
ANW
1 288 ?
P NE
481 472
636
729
491
P WC
39 40
40
50
45
IO W
48 65
63
60
60
1515
4
1191
272
1527
80
50
2000
400
630
2428
253
38
154
482
108
20
15
880
689
1928
376
15
89
500
1510
20
15
20
800
903
2138
48
30
64
500
85
271
2
402
54
234
8
493
205
426
12
615
7
6
2037
4
830
203
1800
90
1185
1
849
170
189
1824
9
730
145
372
2406
3504
228
50
1
4309
274
50
50
2001 mean
107 223
13
15
15
139
16
824 642
970 380
2280 2556
50 452
13
54
60
50
500 1006
226
481
12
489
2
138
141
10
620
1
3
1453 1115
4
3
791 1686
120 133
340 1044
26
279
1504 1301
300 361
50
46
30
11916 9996 12977 11757 12513 11657 12617 11592 15019 10743 12331
P NW 6,072 5,996 6,106 6,602 7,226
P NW 1,583 2,068 2,117 1,892 1,979
7160
2217
6952
1439
6662
1204
6957
1419
7229 6696
900 1682
358
7,655 8,064 8,223 8,494 9,205 9,377 8,391 7,866 8,376 8,487 8378
53
1) All the species except Apostichopus japonicus
In 2001, the last statistics show, if considering the countries with data over 1000 tons, that:
• Indonesia is the first world fishery, with products mostly coming from the pacific western central zone.
• The second in the statistics are U.S.A; but these data seem questionable, as there could be some problem
with the Canadian production, from 1996. Another problem could be the data from the Atlantic Northwest
fishery, which is not documented….
• The third fishery is in Papua-New-Guinea.
• The world total is over 10 000 tons, which corresponds to more than 100 000 tons captured.
• 3 countries are no more reporting, Palau, Tonga and Yemen;
• On the whole, there are 23 countries listed, with among them, 3 countries over 1000 tons, 11 countries
between 1000 and 100 tons and 9 countries under 100 tons.
Figure 2 shows the captures by FAO zones for 2001. Some countries do not appear despite some fisheries,
for example Australia, Bangladesh, Chagos, Venezuela and India.
300
1504
4
848 7*
53
442
5997
1230
122
1090
2
Figure 2: Beche-de-mer production(t)in bold, for 2001, according to FAO zones and different data.
*captures (t) for zone 61
54
For the last decade (1992-2001), the calculated mean catches show:
• Indonesia is the world leader, but there is a small decrease since 1997; more information is given by Tuwo
(in press).
• The second is the Philippines, as it was traditionally (Sachithananthan 1972; Conand 1990, Conand 2004).
The decrease started in 1994 and the present catch is only 1/5 of the previous one. Gamboa (2004) gives
more information about this country.
• The third is the U.S.A., with the issues already raised for 2001
• The fourth is Papua-New-Guinea, with a strong increase since 1997 (see Polon 2004)
• The fifth is Tanzania where the catches regularly decrease since 1997 (see Mmbaga and Mgaya 2004)
On the whole, from the 26 countries listed, the mean catch for the decade is over 1000 tons for 6 countries,
between 1000 and 100 tons for 8 and under 100 tons for 12.
2) Apostichopus japonicus fisheries
In 2001, the last statistics show:
• Japan is the major country for the fishery with 7 229 tons (live weights)
• Rep of Korea is second with 900 tons
• China is appearing with 358 tons in 2001
For the last decade (1992-2001), the calculated mean catches show:
• Japan has remained stable
• Rep of Korea is slightly decreasing
• The data are not available for the period for China.
Table 2: World imports of sea cucumber, fresh/frozen/dried/salted/ in brine, 1995-2001
(Q=TONS; V=US$’000) (after Ferdhouse 2004) Source: FAO FISHDAB
Country
China
Hong Kong
Japan
Korea, Rep
Malaysia
Singapore
Taiwan PC
Thailand
World total
(incl. others)
Q
V
Q
V
Q
V
Q
V
Q
V
Q
V
Q
V
Q
V
1995
5 789
40 898
25
799
7
128
521
755
1 273
5 792
32
102
1996
49
49
5 020
43 376
10
350
36
154
358
564
1 079
5 327
32
90
1997
1
3
4 523
38 147
5
134
16
302
4
1 014
5 291
71
446
1998
9
30
3 975
39 565
5
163
2
23
18
8
859
4 549
78
282
1999
139
265
2 922
33 571
4
121
10
68
21
34
899
4 735
75
417
2000
186
793
4 759
55 533
3
141
29
127
32
24
887
4 514
133
528
2001
2 059
1 229
4 382
50 430
3
81
51
400
2
16
676
3 979
115
504
Q
V
7 653
48 507
6 597
49 987
5 630
44 327
4 946
44 620
4 079
39 331
6 040
61 691
7 299
56 722
55
1.2 Main exporting and importing countries
Exporting countries: as the fisheries for the dried products, presented in part 1.1, are occurring in countries
where there is no, or little, consumption, these countries are also exporting.
The main importing countries are traditionally Hong Kong, Singapore, Taïwan and China; Malaysia also
imports but smaller quantities (Sachithananthan 1972; Conand and Byrne 1993; Conand 1990; Conand 2001;
Conand 2004; Ferdhouse 2004):
Based on FAO (2003), the global imports of fresh, frozen and dried sea cucumber (including salted in brine
but excluding canned products) totaled 7 299 tons in quantity and US$ 56.7 million in value in 2001 (Table 2).
Note that the imports of sea cucumber into Singapore, were not reported in these trade figures.
• Hong Kong (after Ferdhouse, in press and Conand, 2001)
Hong Kong, special Administrative Region of China, is the largest importer of sea cucumber in the international
market since 1930 (Sella and Sella 1940; Sachithananthan 1972; Conand 1989; Conand 1990; Conand and
Byrne 1993; Conand 2001). The market is dominated by imports of dried tropical sea cucumber of all varieties.
The cold water species are imported from the USA and Canada in gutted frozen form for the up markets in
mainland. Imports of sea cucumbers declined by almost 50% in 2000s compared to mid 1990s. The import
market has stabilized at a volume of about 4 000 TONS per annum during the last 6 years. In 2002, imports
recovered to 4 417 tons at a value of HK$ 440 million (US$ 56 million) (Table 3A and 3B). The main suppliers
were Indonesia, the Philippines, Singapore, Papua New Guinea, Solomon Islands, Madagascar and Australia.
For the last few years, supplies have been dwindling from regular sources except from Indonesia. New
supplies from Africa and the Middle East have entered the market. However, the quantity is not sufficient to
offset the lower exports from the other sources.
A survey indicated that in general sea cucumber is perceived as an expensive product. The consumption is
limited to the middle-aged group, festival celebration (Chinese New Year), wedding dinners, banquets etc.
Hence, demand fluctuates according to the age group and most of all by disposable income. The market
preference is similar to the mainland. Consumers in Hong Kong prefer large and medium sized dried skin-on
calcium coated sandfish and teatfish which are the high value species, but also Apostichopus japonicus.
However, for Hong Kong traders the main attraction is the expanding mainland market. In 2002, Hong Kong
re-exported nearly 3 000 tons of sea cucumber which was 67% of the total imports in that year. China was the
largest outlet (72%); all types of sea cucumber are exported to the China market mainly by road and also by
sea depending on the destination. The other markets are Taiwan PC, the USA and some other niche markets
(Table 3C).
As direct imports to China is subject to high import duty and rather complicated procedures, exporters from
other countries prefer to supply to Hong Kong traders. The territory still retains the status of a duty free port
for imported products.
56
Table 3A: Hong Kong: Imports of beche-de-mer (dried, salted or in brine), 1997 – June 2003 (Q=TONS;
V=HK$ 1000) (after Ferdhouse 2004) Source: Agriculture, Fisheries and Conservation Dept., Hong
Kong.
Countries
1997
1998
1999
2000
2001
2002 Jan-Jun 2003
USA
Q
41
44
114
182
90
155
88
V
3 307
3 242
6 032
10 473
5 439
10 318
5 790
Canada
Q
18
20
5
3
59
18
13
V
2 337
2 911
660
80
3 332
1 373
630
UA Emirates
Q
21
11
0.2
21
1
V
600
1 393
13
1 585
0
Yemen
Q
3
3
113
71
V
256
332
11 497
3 831
Taiwan
Q
22
71
41
40
57
119
34
V
2 024
5 300
6 255
7 695
17 705
29 485
9 447
Indonesia
Q
1 097
961
757
1 007
1 060
1 008
429
V
484 424
42 073
31 207
40 907
34 084
31 986
13 467
Philippines
Q
165
467
591
1 070
737
775
268
V
18 931
18 855
31 608
63 751
39 400
39 004
15 109
Korea PR
Q
2
2
3
1
12
V
232
369
273
211
782
Japan
Q
29
53
55
75
103
127
94
V
23 321
41 386
53 593
81 230
90 771 131 763
121 827
China
Q
27
77
30
13
12
27
22
V
1 314
214
1 830
2 074
778
1 218
837
Vietnam
Q
56
47
34
1
3
1
4
V
2 516
2 904
957
215
950
142
448
Maldives
Q
117
23
4
39
29
38
25
V
6 085
1 296
229
2 345
1 626
1 080
1 080
Sri Lanka
Q
76
52
19
65
33
50
49
V
8 982
4 616
1 838
3 732
1 894
2 918
2 441
India
Q
1
2
1
4
2
V
396
523
114
807
356
Malaysia
Q
22
60
19
59
66
124
69
V
1 452
3 090
1 382
3 939
3 677
8 982
5 267
Singapore
Q
479
349
212
345
335
364
149
V
33 471
22 834
15 872
24 005
24 925
28 305
7 969
Mozambique
Q
82
25
1
0
1
37
33
V
1 932
204
76
40
220
3 307
2 558
Madagascar
Q
204
216
154
178
179
169
122
V
28 400
22 080
18 084
17 745
15 497
9 946
4 837
South Africa
Q
47
49
21
28
29
53
34
V
2 303
4 151
1 085
2 188
969
1 035
584
Kenya
Q
2
52
39
20
9
V
148
3 377
1 407
1 873
2 447
Mauritius
Q
3
6
1 716
V
271
1 408
339
Tanzania
Q
182
72
31
115
56
92
40
V
10 853
4 781
5 237
8 708
4 676
5 462
1 613
US Oceania
Q
29
20
12
18
41
V
2 680
2 463
1 789
1 935
-
57
Table 3B: Hong Kong: Imports of beche-de-mer (dried, salted or in brine), 1997 – June 2003 (Q=TONS;
V=HK$ 1000) (after Ferdhouse 2004) Source: Agriculture, Fisheries and Conservation Dept., Hong
Kong
Countries
1997
1998
1999
2000
2001
2002 Jan-Jun 2003
Aust & Oceania
Q
70
39
32
14
22
17
12
V
11 776
6 769
5 737
2 735
3 703
3 383
2 539
Kiribati
Q
4
3
4
9
14
9
1
V
104
264
522
683
1 005
883
192
Tonga
Q
12
V
1 705
W. Samoa
Q
11
4
6
V
1 045
833
533
Australia
Q
63
73
118
139
187
139
59
V
13 008
16 870
23 615
42 061
40 910
32 792
19 154
Solomon Is.
Q
122
252
50
144
260
249
141
V
6 897
12 779
2 641
7 325
14 896
12 027
4 846
Fiji
Q
528
291
166
364
276
162
86
V
26 232
23 956
14 523
28 149
21 770
12 659
4 973
New Zealand
Q
15
8
1
11
31
16
3
V
1 333
469
186
2 227
3 998
1 241
192
Vanuatu
Q
35
25
8
28
16
8
1
V
1 038
1 116
286
1 315
888
401
44
PN Guinea
Q
453
613
336
532
493
368
212
V
33 215
52 684
27 201
45 655
37 405
38 097
23 711
Total
Q
4 523
3 975
2 922
4 759
4 382
4 417
2 222
(incl. minor
V
295 341 306 442 260 425 432 665 393 297 439 628
270 499
exporters)
5788
3907
HONG-KONG
300
550
40
SINGAPORE
TAIWAN
34
1051
759
Total Imports
715
Total Re-exports
Flux of bêche-de-mer from reciprocal exchanges
between markets
Figure 3: Reciprocal exchanges of product between the main markets (from Conand 2001)
58
Table 3C: Hong Kong: Re-export of beche-de-mer (dried/salted/in brine), 1997 – June 2003
(Q=TONS; V=HK$1000) Source: Agriculture, Fisheries and Conservation Dept., Hong Kong.
Country
USA
Canada
France
UK
Taiwan
Indonesia
Korea RP
Thailand
Japan
China
Malaysia
Singapore
Australia
Total
Q
V
Q
V
Q
V
Q
V
Q
V
Q
V
Q
V
Q
V
Q
V
Q
V
Q
V
Q
V
Q
V
Q
V
1998
1999
2000
2001
2002
21
2 938
27
3 779
224
20 797
50
4 616
1
302
2 780
97 438
9
714
37
5 769
1
277
3 174
139 691
17
2 544
16
2 722
0.001
158
15 479
10
236
50
4 780
31
5 265
0.1
46
2 268
78 159
22
2 550
81
12 293
3
288
2 658
125 099
23
2 880
13
2 717
209
25 164
0.1
13
82
7 102
30
6 005
1
711
3 771
176 034
21
2 866
70
9 854
1
79
4 221
233 885
38
2 750
27
3 395
0.001
28
117
9 927
62
4 294
40
6 555
1
325
3 543
141 171
6
667
28
6 122
2
359
3 867
176 792
106
6 409
14
3 906
152
16 662
36
2 703
40
7 656
1
213
2 127
73 903
6
1 046
19
4 253
2
203
2 944
130 575
Jan-Jun
2003
48
3 657
8
1 232
39
4 488
10
644
8
2 000
0.2
92
938
25 544
1
78
10
2 664
2
129
1 305
49 288
• Singapore (after Ferdhouse, 2004 and Conand, 2001)
Sea cucumber is a preferred seafood delicacy of the highest order, a positioned shared with dried sharkfins.
However, sea cucumber is expensive, thus followed the demand pattern dictated by consumer's disposable
income.
From Singapore a large share of imports are re-exported to other destinations. Imports fluctuated from 820
tons in 1997 to 629 tons in 2000 due to the economic recession in the region. Hong Kong was the main supply
source. The other exporters to this market were India, Yemen, the USA and South Pacific island countries.
During late 1990s, imports increased from Madagascar, Tanzania consisted of cheaper quality sandfish and
some white teatfish. The best quality products come from Australia and the other pacific sources. Imports
also take place from Indonesia which are not reflected on the official statistics (Table 4A and 4B).
59
Table 4A: Singapore: Imports of beche-de-mer (dried/salted/in brine), 1997-2000 (Q=TONS;
V=S$ 1000) (after Ferdhouse 2004) Source: National Statistics, Singapore.
1997
1998
1999
2000
Country
Q
V
Q
V
Q
V
Q
V
Australia
12
NA
7
585
14 1 185
4
337
New Zealand
5
NA
13
820
12 1 428
19 1 047
China RP
13
NA
21 1 437
4
385
5
853
Taiwan
86
NA
75 3 852
16
865
27 1 340
Hog Kong
201
NA
73 7 374
93 9 972
104 12 964
India
97
NA
58 3 332
43 2 837
82 6 732
Sri Lanka
36
NA
30 2 282
18 1 203
15 2 388
Malaysia
2
NA
5
111
5
317
3
296
Myanmar
1
NA
1
83
Vietnam
3
317
1
162
Fiji
20
890
Maldives
23
NA
18 2 139
11
974
10 1 644
Papua New
2
80
1
70
1
129
Guinea
Solomon Islands
4
NA
82
Mauritius
5
NA
4
224
4
170
Kenya
7
NA
6
275
2
76
Madagascar
10
137
5
349
UAE
9
NA
1
71
5
288
7
369
Yemen
2
NA
9
430
23
506
21
382
USA
3
82
57 2 255
49 2 751
Oceania
12
443
101 3 840
122 6 218
Total (incl.
820
538 32 448
692 37 221
629 48 145
others)
Table 4B: Singapore Exports of beche-de-mer (dried/salted/in brine), 1997-2000
(Q=TONS; V=S$ 1000) (after Ferdhouse 2004) Source: National Statistics, Singapore
Country
Hong Kong
Malaysia
Taiwan
Myanmar
Thailand
USA
Brunei
Total (incl.
others)
1997
Q
V
502
255
116
19
1
-
1998
Q
V
236
3 543
146
3 943
81
3 359
20
586
2
139
-
1999
Q
V
161
3 111
238
6 247
132
6 146
8
177
1
87
-
2000
Q
V
295
4 351
214
7 143
138
5 236
17
345
2
111
-
895
542
586
723
-
12 251
60
16 530
18 356
Although the market demands high value products, the small population in Singapore (2.3 million) is not able to
support the total import. Thus a loin share gets re-exported to Hong Kong, Malaysia, Taiwan PC, Myanmar
and Thailand. AFTA (ASEAN Free Trade Agreement) also allows re-exports to the ASEAN member countries
(Malaysia, Thailand, Myanmar). While exports to Malaysia consist of medium grade sandfish of different sizes
and a small quantity of teatfish, high quality products are exported to Taiwan PC.
Domestic consumption of sea cucumber in Singapore has been low during the last few years. The economic
recession since 1998 coupled with the SARS problem in 2002-2003, have affected the domestic seafood
consumption.
• China (after Ferdhouse, 2004)
China is the largest market for sea cucumber. However, the actual trend in the market is not reflected on the
published data. The official trade statistics from Hong Kong indicated that re-exports to mainland varied
between 2 000 - 3 500 tons annually during 2000-2002 (Table 5). In 2001, re-exports to China from Hong
Kong SAR were 3 543 tons.
The 2001 official statistics from China reported an annual imports of 2 059 tons according to which only 13
tons came from Hong Kong (Table 5). Imports from Indonesia in that year were 1 146 tons - 50% of the total
official imports in that year. The other major suppliers were the Philippines (791 tons), Korea (21 tons) and
Thailand (55 tons). Minor supplies came from Canada and Russia.
Table 5: China: Imports of sea cucumber, frozen/dried/salted/in brine, 1999-2001
(Q=TONS; V=US$’000) (after Ferdhouse 2004) Source: Bureau of Fisheries, PR China.
Country
Russia
Ecuador
Philippines
South Korea
Papua New
Guinea
Canada
Madagascar
USA
South Africa
Japan
Sudan
Thailand
Hong Kong
Indonesia
Chile
Total
1999
Q
V
0.5
7 500
0.09
525
28.8
23 599
0.06
1 300
14.63
7.19
9.47
14.28
50.19
9.12
139.15
22 107
13 793
10 293
19 795
154 001
4 766
265 306
2000
Q
V
0.85
8 500
45.02 348 241
12.34
76 766
10.58
27.17
13.76
44.06
186.24
61
24 031
65 397
54 509
84 846
793 045
2001
Q
V
1.20
6 000
1.16
11 258
791.48
489 250
21.10
107 840
0.62
4 992
17.54
0.94
6.41
1.08
0.02
55.91
13.50
1 146.41
1.20
2 059.05
41 385
2 560
40 276
1 642
1 023
18 780
11 369
488 502
720
1 229 799
Taking into consideration the exports from Hong Kong to this market, the annual import into China
could be around 5 500 tons. This shows the importance and supremacy of China in the international market for
sea cucumber. It is important to note that the market is capable to absorb all kinds and qualities of sea
cucumber due to the varied degrees of purchasing power. Per capita income of the population in southern
provinces is much higher than the average national per capita income of the country. Hence both high and low
valued species and qualities of sea cucumbers are imported into China for domestic consumption.
• Taiwan (after Ferdhouse, 2004 and Conand, 2001)
Demand for high value fish and fishery products is relatively high in Taiwan. This is related to high per capita
income and the traditional influence of the Fijian and Teochew provinces (the origins of the Taiwanese). Household
consumption of processed sea cucumber is high, although the species are not popular with highlanders.
Traditionally the Taiwanese market has preference for various kinds of spiky sea cucumber which are both
tropical and coldwater species. The coldwater prickly redfish are imported from Alaska and Canada in frozen
form. Taiwan also imports frozen sea cucumber from Peru which are processed into dried
Table 6: Taiwan: Imports of beche-de-mer, 1997-2002 (Q=TONS; V=NT$1000) (after
Ferdhouse 2004) Source: Fisheries Statistical Year Book, Taiwan PC.
Year
1997
1998
1999
2000
2001
2002
Products
Spiked
Frozen
Dried
Salted/in brine
Total
Frozen
Dried
Salted/in brine
Total
Frozen
Dried
Salted/in brine
Total
Frozen
Dried
Salted/in brine
Total
Frozen
Dried
Salted/in brine
Total
Frozen
Dried
Salted/in brine
Total
Q
39
39
41
41
37
37
32
32
20
20
12
12
Others
V
19 675
19 675
25 763
23 763
25 033
25 033
23 126
23 126
16 089
16 089
10 468
10 468
62
Q
348
658
14
1 020
274
530
1
805
299
508
54
862
295
517
44
855
198
426
624
208
733
62
1 002
V
47 762
90 039
1 562
139 449
42 812
81 581
163
124 572
43 343
75 592
4 535
123 489
44 594
68 406
4 507
117 507
35 483
62 237
97 720
38 429
89 047
9 599
137 075
Total
Q
348
697
14
1 059
274
371
1
846
299
545
54
899
295
549
44
887
198
446
32
676
208
745
62
1 015
V
47 762
109 714
1 562
159 124
42 812
107 344
163
150 335
43 343
100 625
4 535
148 522
44 594
91 532
4 507
140 633
35 483
78 326
3 736
117 545
38 429
99 515
9 599
147 543
products for the domestic market. Demand for high value sandfish is rather limited but increasing slowly
through supplies from Hong Kong. Consumption of sea cucumber was low during the economic recession in
1998-2000. However, imports (Table 6) recovered since 2001 and totaled 1 015 tons in 2002, against 624
tons in 2001. Nearly 28% of these were frozen products imported from coldwater sources. Imports of tropical
species take place from India, Indonesia, the Philippines and from mainland China.
Import duty on sea cucumber is high in Taiwan. The tariffs also differ according to the species that range from
20-40% on the invoice value. The spiky varieties enjoy lower tariff compared to the other species. Import
duty on frozen products is also lower than that of dried/salted products. Unlike Hong Kong, a few importers
dominate the market in Taiwan. The market also demands high quality products.
•Malaysia (after Ferdhouse, 2004)
Malaysian population is multi-racial where Chinese are the second largest group. The country’s population has
increased since then to 23 million in 2003 but the ratio of Chinese origin people has declined, as the average
family size has became smaller than before. Hence the market for sea cucumber in Malaysia has shrunken.
Consumption of sea cucumber among the ethnic Chinese in Malaysia is not as high as Singapore or Hong
Kong. The market imports a small volume of fresh/chilled and frozen sea cucumber from the neighboring
Indonesia but dried products are the predominant type. Nearly half of the imported sea cucumber is reexported to other markets. Imports in 2002 were low at 160 tons, compared to over 500 tons in 1998. The
major share of supplies came from Indonesia followed by Hong Kong and China. Dried sea cucumber were
re-exported from Malaysia to Hong Kong, Taiwan, Singapore and Thailand .
Local consumption is related to the festive season and occasions (wedding/birthday etc.) due to the price
factor. Households buy processed/soaked products particularly during the Chinese New Year for family
dinner. These are sold at traditional wet markets, some supermarkets and also at Chinese wholesale shops
who sell other dried fishery products and Chinese herbs. In Malaysia the Chinese traders dominate the import
and domestic markets.
• Reciprocal exchanges between the main markets
The Reciprocal exchanges take place between some of the markets, leading to an over-evaluation of the world
tonnage. This important characteristic of this market has been studied by Conand (2001). It is not easy to
understand and complicates the evaluation of catches from the market data. In fact the same product can
appear twice, or even three times, in the imports if it has been re-exported. As observed earlier, though the
detail of the figures do differ, between Hong Kong and Singapore the data spread is the same interval. The
general flux is always from Singapore to Hong Kong. The reciprocal exchanges between Taiwan and the other
markets are limited. They are non-significant with Hong Kong and minor with Singapore. The interaction is
mainly between Hong Kong and Singapore (Figure 3, from Conand and Byrne 1993).
1.3 Sources of sea cucumbers (i.e. wild or aquaculture), origins
The natural resource has been the only source of sea cucumbers for a very long time, as the Chinese have
thought them for more than thousand years and the Japanese for some hundred years (Akamine 2004).
The aquaculture experiences in Japan and in China for Apostichopus japonicus date back to the years 50,
but have only recently been increased to an industrial size in the Northeast of China (Jiaxin 2003; Jiaxin 2004;
Yaqing C. 2004). In the issue 19 of the Beche-de Mer Bulletin (S.P.C.) two Chinese companies are presented,
showing the present development and promising prospective. The country data are not available to the author's
knowledge, but it is essential to follow this production, its development and consequences.
63
Some tropical Indian and Western Pacific countries are developing aquaculture for Holothuria scabra (Indonesia
see Tuwo 2004; India see James 2004; the Solomon see Battaglene 1999; Madagascar see Rasolonofirina et
al. 2004. In Ecuador, Isostichopus fuscus is the targeted species (Mercier et al. 2004).
A particular attention should be given in the future to follow these activities and their impact.
1.4
Trade routes, and principal species in trade
Trade routes are very similar in the tropical indo-Pacific countries. The processing is generally made in the
local communities by the fishermen, their wife or local collectors. Then, the Chinese merchants buy the products,
and eventually re-do some steps of the processing if necessary (drying for example). They then ship the
products to the main markets (see part 1.2), according to their commercial or family relations. Re-exports and
subsequent double reporting of trade figures is a characteristic of this trade (Conand 1990, 2001).
Principal species in trade: they have been presented in the document 1, prepared for this workshop by C.
Conand (see Table 1 list of species, according to FAO zones and commercial value).
In the traditional tropical Indo-Pacific fisheries, there are about 30 species of some commercial interest but
only 13 in categories 1 (high value) and 2 (medium value). Altogether at the world scale, there are about 42
exploited species, and a few more could be added in the future.
The S.P.C. handbook (1994) shows photographs of the live and dried specimens and details the processing
methods.
2. Description of the main utilization of sea cucumbers as food, in Traditional East Asian Medicines,
live aquarium trade, and other uses
2.1 Body wall processed as food
The main utilization of sea cucumbers as food is the consumption of the body wall, prepared as dried product
then soaked before cooking; other preparations of the tegument also exist and appear in some statistics:
•
Dried product (trepang, beche-de-mer, hai-som) The Chinese are the main consumers. China is the
largest market and consumer of sea cucumber. Unfortunately, the level of total annual supply in this market
is not yet known. Most of the imported sea cucumber in China comes through Hong Kong. The other
major consuming countries and territories in the region are Hong Kong, Taiwan, Singapore and Malaysia.
In the minor markets in North America (USA and Canada) and Western Europe, consumption of sea
cucumber is rather occasional, compared to other seafood preferred by the Oriental people living in those
countries.
•
Boiled: some imports appear in the statistics of several countries as boiled or salted (see tables).
•
Raw: Japan is the market for raw sea cucumbers. The body wall is consumed raw, but also the preserved
gonads (konoko) and the intestines (konowata) are delicacies.
•
Traditional food in Pacific islands: in Fiji, there is a local market for Holothuria scabra which is sold to
be cooked in coconut milk (see one photograph in Conand 1990).
64
2.2 Other organs used for human consumption
• Japanese eat raw sea cucumber body wall, but they also like the preserved gonads (konoko) and the
intestines (konowata) are delicacies.
• The fresh gonads are consumed in some South Pacific Islands as Cook Islands where "matu" the ripe
gonads of male Holothuria leucospilota are harvested traditionally (Zoutendyk 1989).
• Various species are eaten pickled in limejuice in some Pacific Islands, but the subsistence use of the
intestines of Stichopus hermanni in Palau and Pohnpei is of interest and has been described by Lambeth
(2000). The sea cucumbers are collected during the morning low-tide when the intestines are clear of sand,
before feeding, and cut in two pieces or a small slit is done. The intestines are removed and the animal
rejected to the reef to regenerate; the women believe that they regenerate very fast.
2.3 Traditional East Asian Medicines
East Asia countries have utilized sea cucumbers as medicines since ancient times.
For Malaysia Baine and Choo (1999 a and b) and Choo (2004) have given some information's. Malaysians
value sea cucumbers for their medicinal benefits. Malays have traditionally utilized certain species of Stichopus
(locally known as gamat) for their medicinal properties and traditional medicines processed from gamat are
used in wound healing, treatment of stomach ulcers and as a painkiller. Apart from the traditional gamat water
and oil, sea cucumbers have been incorporated into products, which include juice, balm, liniment oil, cream,
toothpaste, gel facial wash, body lotion, facial wash and soap. Sea cucumber is cholesterol-free. It is high in
protein (55% of dry body weight) and contains 10-16% mucopolysaccharides (substances used for building
cartilage) and saponins; it is helpful in reducing arthritis pain and arthralgia (due to the mucopolysaccharides
content) and pharmacology studiesindicate that the saponins of sea cucumber have anti-inflammatory and
anticancer properties (Dharmananda, undated).
Scientists from the University of Malaya working on S. hermanni reported on the painkilling, anti-inflammatory
and anti-itching properties of this sea cucumber (Awaluddin 2001). Research carried out by Malaysian scientists
indicated that three types of antimicrobial agents, namely atratoxin A, B1 and B2 were found in H. atra, and
these agents exhibited high activity against various species of yeast and fungi. Ethanol extracts from H. atra
have antifungal properties.
The Chinese have long regarded sea cucumbers as a general health tonic, beneficial for treating tendonitis and
arthritis, and as an aphrodisiac, among many other medicinal claims (Jiaxin 2003; Jiaxin 2004). Eating Trepang
is a hobby of Chinese. The history can be traced back to Ming Dynasty (1368-1644 BC.) at least. Afterwards,
sea cucumber was recognized as a tonic and a traditional medicine of animal source recorded in so many
ancient litterature, from Ming Dynasty to Qing Dynasty (Fan 2001). According to analysis by principles of
traditional Chinese medicine, the sea cucumber nourishes the blood and vital essence (jing), tonifies kidney
(treats disorders of the kidney system, including reproductive organs), and moistens dryness (especially of the
intestines). It has a salty quality and warming nature. Common uses include treating weakness, impotence,
debility of the aged, constipation due to intestinal dryness, and frequent urination. Thereunder the tradition, the
preference of Chinese eating sea cucumber is derived from the belief of a tonic, but than seafood. Hence, the
popular Chinese name for sea cucumber is haishen, which means, roughly, ginseng of the sea.
65
other delicacies, such as shark fin and bird’s nest soup, as a disease preventive and longevity tonic. From the
nutritional viewpoint, sea cucumber is an ideal tonic food. It is higher in protein than most any other food
except egg whites (at 99%), and it is lower in fat than most foods (Table 1). While the amino acids, especially
necessary amino acids and necessary trace elements is good enough for healthy of people, who suffer some
illness.
For modern applications, the dried or extracted sea cucumber is useful as a nutritional supplement, prepared in
capsules or tablets. The fully dried material has a protein concentration as high as 83%. From the Western
medical viewpoint, the reason sea cucumber is valuable is because it serves as a rich source of the polysaccharide
condroiton sulfate, which is well-known for its ability to reduce arthritis pain: as little as 3 grams per day of the
dried sea cucumber has been helpful in significantly reducing arthralgia. Its action is similar to that of glucosamine
sulfate, which is useful for treating osteoarthritis. Sulfated polysaccharides also inhibit viruses; there is a Japanese
patent for sea cucumber chondroitin sulfate for HIV therapy.
Chinese studies reveal that sea cucumbers also contain saponin glycosides. These compounds have a structure
similar to the active constituents of ginseng, ganoderma, and other famous tonic herbs. Additional Chinese
studies indicate anticancer properties of both the sea cucumber saponins and the polysaccharides.
Natural substances
There are many references on the chemical composition of sea cucumbers and the research looking for new
compounds, molecules, or bio-active substances, is progressing fast, but some of the results stay confidential,
as the pharmaceutical industries are involved.
A synthesis has been presented by Verbist (1993) for the Echinoderms, where the following substances have
been detected in sea cucumbers; the references are given in tables:
• Hematolytic substances are found in 38 species of holothurians
• Hemaglutinating substances found in 5 species of holothurians
• Cytotoxic and antitumoral substances found in 31 species; 35% of the extracts are giving a positive response.
The cytotoxic compounds have been isolated (ex: holothurin A and B, Stichoposide, Cucumarioside).
• Antimicrobial and antifungal activities have been shown with many extracts.
• Immune factors are found in holothurins, which are also active on nerve and muscle.
• Other substances (saponins, muccopolysaccharides, etc.) have been less studied but are present.
Another more recent synthesis is more focalized on the triterpene glycosides from holothurians (Kalinin et al.
1996).
These pharmaceutical researches are an important, but not well documented field.
2.4 Live aquarium trade
To the author's knowledge, there is no live aquarium trade. The main reason could be that the body wall
contains toxins, which are able to kill other animals, if they are put in contact with sea cucumbers, or the sticky
cuvierian tubules for the species, which have these organs.
66
2.5 Other uses
Toxins contained in the body wall of tropical species (ex: Holothuria atra) are traditionally used for poisoning
small fish in tide pools (Conand 1990).
Dendrochirotes as they are filter-feeders are said to be useful as biofilters.
3. Information or recent examples of illegal, unreported or unregulated fisheries and trade, with an
indication of the overall scale, trends, and the impacts on sea cucumber stocks
Information about of illegal, unreported or unregulated fisheries and trade is not easily accessible. From a
questionnaire widely distributed in many countries, Baine (2004) has given a summary of the replies presented
here and organised in Table 7:
Table 7. Information on illegal fishing supplied by respondents to the questionnaire
exercise (after Baine 2004).
Country
Australia
(Northern)
Brazil
China
Cook Islands
Cuba
Ecuador
(Galapagos)
Indonesia
Kiribati
Malaysia
Marshall Islands
N. Caledonia
(NP)
N. Mariana
Islands
Papua New
Guinea
Philippines
Solomon Islands
Vietnam
Are you aware of illegal sea-cucumber fisheries and trade
activities?
N
Y Some private collection and consumption (Japanese)
N
N Suspicion that an opportunistic fishery may exist from transient
fishermen.
N
N Not at present.
Y Indonesian fishermen fish in Australian waters.
Y Fishing in foreign waters, smuggling pout of the country,
deliberate under reporting
N Amount exported is not high.
Y Especially not sparing spawning and immature individuals.
Y Occurs on some atolls although species remain abundant
Y Fishermen do not declare their activities. No regulation of
trade.
Y Some personal use despite moratorium.
Y Mainly through one vessel in a remote area of the country
N No clear regulations so no illegal fishing. Fishers do illegally
Y fish Malaysian waters.
Illegal fishing by trawl and some probable illegal exports.
N All exporters are licensed – no limit on tonnes exported
Y Regulation needed.
67
Additional information about of illegal, unreported or unregulated fisheries and trade includes:
• Historically, the Galapagos marine reserve in Ecuador has suffered high levels of illegal fishing,
coinciding with increased migration to the islands. Fishers have been provided with boats and motors
financed by mainland and foreign traders (Martinez 2001). The impetus to fish has been high and
violent clashes with the National Park Service have occurred in the past. The Galapagos history of the
fishery management will be detailed in Sant's document prepared for this workshop (Sant 2006).·
• Illegal fishing has also been recorded in other countries: Madagascar (Irwing 1994), Malaysia (Baine
and Choo 1999), Mexico (Ibarra and Soberon 2002), Papua New Guinea (Kinch 2002) and Venezuela
(Rodriguez and Marques Pauls 1998).
• The questionnaire exercise (Table 7) additionally identifies some illegal activities in other countries
New Caledonia, Vietnam, the Philippines, Indonesia, the Marshall Islands and Brazil. But, illegal
fishing is not thought to occur in the Cook Islands, Kiribati, China, Ecuador (at present), and the
Northern Territory of Australia.
• Many references are also found in the Beche-de-Mer Bulletins.
The complexity of trade routes for sea cucumbers, often involving import and subsequent re-export, or
transshipment ports that export mixed shipments of different origins makes it difficult to determine the country
of origin. It is also difficult to determine whether the harvest was legal, as shipments often include multiple
species that are difficult to differentiate when dried, and those countries that have established regulations for
holothurian fisheries generally prohibit the harvest of selected species or in specific locations. Furthermore, the
processed product generally passes from the producing country to the main world distribution centers (Hong
Kong, Singapore and Taiwan) before being imported to the consumer country. Trade statistics are further
complicated by the variety of products available in international markets, including several types of dried
holothurians (spiked & not spiked), as well as frozen, live, fresh or chilled, and salted or in brine.
Illegal sea cucumber fishing is not a prolific problem in countries with this resource. However, being such a
lucrative market, it has caused major problems in certain areas and is a point important for the discussion in the
CITES perspectives.
4. Examples of sea-cucumber-bycatch and indications of scale and impact
In most tropical countries, fishing is done by hand, at low-tide wadding on the reefs or bottom, by snorkeling
and in some cases by scuba-diving (S.P.C. 1994; Conand 1999). These techniques are very selective and
therefore there is no by-catch. In a few cases dredging or trawling are used, for example in Madagascar, and
it has been reported to the author that large Holothuria scabra are found with prawns.In temperate countries,
dredging is used. In Japan Apostichopus japonicus can by collected with different fishing gears but the fishery
is regulated (Choe 1963). In Quebec (Canada) Cucumaria frondosa (Hamel and Mercier 1999) are
accidentally dredged during the scallops harvest season aand returned to sea where most die. The exploitation
was suppose to start on this by-catch. Inin Russia, C. japonica are also collected using dredges, but this is
very little documented.
68
5. Socio-economic aspects of the sea cucumber fishery, including relative economic importance, a
description of the chain of custody, values and prices, and market trends.
5.1. Socio-economic aspects
Traditional fisheries. The sea cucumber fisheries were traditionally situated in less developed counties of the
tropical Indo-West Pacific. These small-scale artisanal fisheries do not necessite sophisticated gears, nor ice
and were an important source of incomes for the villagers. A participative management, with all the actors
trying to collaborate, has thus been encouraged in Madagascar, but with the shortage in money, this program
has not been sustainable (Rasolofonirina, and Conand 1998; Conand, De San, Refeno,,Razafintseheno, Mara,
Galet-Lalande and Andriajatovo 1998; Conand 1999).
Table 8: Prices of Sea Cucumber in the International Market, October 2003 (after
Ferdhouse 2004). Source: INFOFISH Trade News, 1 October 2003.
Products
White teatfish, skin-on, 3-5
pc/kg
H. fuscogilva
- Grade-A
- Grade-B
Prickly Redfish, 6-15 pc/kg
Thelenota ananas
Black teatfish, 3-5 pc/kg
- Grade-A
- Grade-B
Stonefish
Sandfish, Grade A
10-30 pc/kg
15-40 pc/kg
Greenfish 50-120 pc/kg
Stichopus chloronotus
Surf Redfish, 15-35 pc/kg
Actinopyga mauritiana
Tigerfish, 25-55 pc/kg
Brown Sandfish, 25-110 pc/kg
Bohadschia marmorata
Curryfish
Stichopus hermanni
Elephant Trunkfish, 3-8 pc/kg
Lollyfish
US$/kg
Market
Origin
23.00
13.00
c&f South East
Asian Ports
South Pacific
15.00
18.00
10.00
18.00
48.00
56.00
40.00
25.00
11.00
3.00
5.00
19.00
5.00
1.50
69
Australia
c&f Singapore
Indonesia
South Pacific
Recent fisheries. The Ecuador sea cucumber fishery for Isostichopus fuscus (Galapagos and mainland)
with its numerous conflicts in the first years of development, is a good example of the socio-economic impacts.
It is described in many papers (see Martinez 2001; Sant 2004 among other) and it has temporarily been solved
by putting recently the species on CITES Appendix III.
In the different countries and fishery context, it is important to give more attention to the socio-economic issues
of these fisheries, to help sustainable management measures being introduced and evaluated.
5.2. Values and prices and market trends (after Conand 1990 and Ferdhouse 2004)
Prices of dried sea cucumber in the international (Table 8 for 10/2003) as well as domestic marketsvary
according to the species (high, medium and low value), sizes and quality of the species. Data have been
presented for the period 1980 in New Caledonia and the South Pacific (Conand 1989; Conand 1990).
Presently, sandfish fetches the high-life prices, the lowest are offered for lollyfish.Over the decade the ranking
of the species has also changed. Some medium value species have moved to the category of high value species
as supplies of sandfish, the high value species as teatfish are getting scarce due to low supplies. In the Hong
Kong market for 2001-2003) (Table 9), the average import prices of Australian origin sea cucumber have
been the highest in recent years due to the species and quality factor. A similar trend is also observed for the
pacific origin sea cucumber. The Hong Kong market also controls international market pricesof sea cucumber.
However, quality is the main factor that determines prices of sea cucumber in general.
Outside China the difference between the import and retail prices is very wide for all categories of sea cucumber.
For example, in Malaysian market the retail price of quality dried sandfish is around US$110/kg. The retail
price of processed frozen wet sea cucumber is US$ 23-24/kg. A similar trend is also noticed in the other
markets in Asia.
Table 9: Hong Kong: Average import prices of Sea Cucumber, 2001-January/June 2003
(US$/kg) (after Ferdhouse 2004). Source: Agriculture, Fisheries and Conservation
Dept., Hong Kong.
Country
2001
2002
Australia
Indonesia
PNG
Philippines
Singapore
Sri Lanka
Madagascar
South Africa
Mozambique
Tanzania
Fiji
Solomon Islands
India
Maldives
28.05
4.12
9.73
6.85
9.54
7.36
11.10
4.28
28.21
10.71
10.11
7.35
25.86
7.19
30.25
4.07
13.27
6.45
9.97
7.48
7.55
2.50
11.46
7.61
10.02
6.19
22.82
3.64
70
January-June
2003
41.62
4.02
14.34
7.23
6.86
6.39
5.08
2.20
9.94
5.17
7.41
4.41
5.54
6. References
The SPC Beche-de-mer Information Bulletins regularly published as issues (SPC) and immediately put on the
web http://www.spc.int/coastfish/news/BDM/23/index.htm are key-reference materials. They include original
contributions and abstracts of the recent literature on holothurians.
The statistics published yearly by F.A.O. and the monthly published Infofish trade News are very useful.
Akamine J. 2004. Historical overview on holothurian exploitation, utilization and trade in Japan. In A.
Lovatelli, C. Conand, S. Purcell, S. Uthicke, J.-F. Hamel & A Mercier, eds. Advances in sea cucumber
aquaculture and management. FAO, Rome. Fisheries Technical Paper No. 463, 425 pp.
Awaluddin, A. 2001. Pharmaceuticals. p.118-119. In: The Encyclopedia of Malaysia: The Seas. Ong, J. E.
Baine, M. and P. S. Choo. 1999. Sea cucumber fisheries and trade in Malaysia. p.49-63. In: The
conservation of sea cucumbers in Malaysia- their taxonomy, ecology and trade: proceedings of an
international conference. Department of Agriculture, Kuala Lumpur, Malaysia. February 1999. HeriotWatt University.and W. K. Gong (eds.). Editions Didier Millet, Kuala Lumpur.
Baine M. 2004. From the sea to the market place: an examination of the issues, problems and opportunities
in unravelling the complexities of sea cucumber fisheries and trade. In A. Lovatelli, C. Conand, S. Purcell,
S. Uthicke, J.-F. Hamel & A. Mercier, eds. Advances in sea cucumber aquaculture and
management. FAO, Rome. Fisheries Technical Paper No. 463, 425 pp.
Baine M. and P.S. Choo. 1999. Sea cucumber fisheries in Malaysia, towards a conservation strategy. BecheDe-Mer Information Bulletin 12: 6-10.
Baine, M. (ed.) 1999. The conservation of sea cucumbers in Malaysia: Their ecology, taxonomy and trade:
proceedings of an international conference. Department of Agriculture, Kuala Lumpur, Malaysia.
February 1999. Heriot-Watt University. 82p.
Battaglene, S. C. 1999. Culture of tropical sea cucumbers for the purposes of stock restoration and
enhancement. p.11-25. In: The conservation of sea cucumbers in Malaysia- their taxonomy, ecology and
trade: proceedings of an international conference. Department of Agriculture, Kuala Lumpur, Malaysia.
February 1999. Heriot-Watt University.
Bruckner AW, Johnson KA and Field JD 2003. Conservation strategies for sea cucumbers: can a CITES
Appendix II listing promote international trade? Beche-de-mer Information Bull.18:24-33
Choe S., 1963 - Biology of the Japanese Common Sea Cucumber Stichopus japonicus, Selenka. Pusan
National University, Pusan : 226 p. (en japonais).
Choo P-S. 2004. Fisheries, Trade and Utilization of Sea Cucumbers in Malaysia. In A. Lovatelli,
C. Conand, S. Purcell, S. Uthicke, J.-F. Hamel & A. Mercier, Eds. Advances in sea cucumber
aquaculture and management. FAO, Rome. Fisheries Technical Paper No. 463, 425 pp.
Conand, C. 1989. Les holothuries aspidochirotes du lagon de Nouvelle-Calédonie : Biologie, Ecologie et
exploitation. Etudes et thèses, ORSTOM: 393 p.
Conand, C. 1990. The fishery resources of Pacific island countries. Part 2: Holothurians. F.A.O. Fisheries
Technical Paper, Rome, No. 272 (2): 143 pp.
Conand, C. 1998. Overexploitation in the present sea cucumber fisheries and perspectives in mariculture.
In: Echinoderms: San Francisco (Eds. R. Mooi and M. Telford): 449-454.
Conand C, 1999. Manuel de qualité des holothuries commerciales du Sud-Ouest de l’Océan Indien. PRE/
COI: 39p.
Conand C., 2001. Overview of sea cucumbers fisheries over the last decade - what possibilities for a
durable management ? : 339-344, in: Echinoderm 2000, Barker M. (scientific ed.), Balkema, Swets &
Zeitlinger:, The Netherlands.
71
Conand C., 2004. Present status of world sea cucumber resources and utilisation: An international overview.
In A. Lovatelli, C. Conand, S. Purcell, S. Uthicke, J.-F. Hamel & A. Mercier, eds. Advances in sea
cucumber aquaculture and management. FAO, Rome. Fisheries Technical Paper No. 463, 425 pp.
Conand, C. and Byrne, M. 1993. A review of recent developments in the world sea cucumber fisheries.
Marine Fisheries Review 55: 1-13.
Conand C., M de San, N.Galet-Lalande, H.Randriamiarana & G.Razafintseheno 1997 - Sea cucumbers in
Madagascar: exploitation difficulties and durable management S.P.C. Bêche-de-mer Information Bull., 9
:4p
Conand C , M De San, G. Refeno, G.Razafintseheno, E. Mara, Galet-Lalande N. & S. Andriajatovo 1998 Gestion durable de la filière holothuries a Madagascar. Bêche-de-mer Information Bull., 10: 7-9.
Dharmananda, S. undated. Sea cucumber: food and medicine. http://www.itmonline.org/arts/seacuke.htm
Fan H. 2001. Sea cucumber: Ginseng of sea. <Zhongguo Marine Medicine>, 82(4): 37-44.
FAO 1994 to 2003. Fishery statistics 1992 to 2001. Vol. 68: Catches and landings. FAO Rome.
Ferdouse F. 1999. Beche-de-mer markets and utilisation.. Beche-de-mer Information Bulletin 11: 3 – 8.
Ferdouse F. 2004. World markets and trade flows of sea cucumber/beche-de-mer. In A. Lovatelli, C. Conand,
S. Purcell, S. Uthicke, J.-F. Hamel & A. Mercier, eds. Advances in sea cucumber aquaculture and
management. FAO, Rome. Fisheries Technical Paper No. 463, 425 pp.
Gamboa R., Gomez L., Nievales M.F., Bangi H.G. Juino-Menez M.A. 2004. The status of sea cucumber
fisheries and mariculture in the Philippines. In A. Lovatelli, C. Conand, S. Purcell, S. Uthicke, J.-F. Hamel
& A. Mercier, eds. Advances in sea cucumber aquaculture and management. FAO, Rome. Technical
Paper No. 463, 425 pp.
Hamel J-F. and Mercier A. 1999. Recent developments in the commercialisation of the northern sea cucumber
Cucumaria frondosa. Beche-de-mer Information Bulletin 11: 21-22
Ibarra A.A. and G.R. Soberon. 2002. Economic reasons, ecological actions and social consequences in the
Mexican sea cucumber fishery. Beche-De-Mer Information Bulletin 17: 33-36.
Infofish. Infofish Trade News.
Irwing, M.A. 1994. Fishing beche-de-mer in Madagascar. Beche-De-Mer Information Bulletin 6: 10-11.
James D.B. 2004. Captive breeding of the sea cucumber Holothuria scabra from India. In A. Lovatelli,
C. Conand, S. Purcell, S. Uthicke, J.-F. Hamel & A. Mercier, eds. Advances in sea cucumber aquaculture
and management. FAO, Rome. Fisheries Technical Paper No. 463, 425 pp.
Jiaxin C. 2003. Overview of sea cucumber farming and sea ranching practices in China. Beche-de-mer
Information Bulletin 18: 18-23
Jiaxin C. 2004. Present status and prospects of sea cucumber industry in China. In A. Lovatelli, C. Conand,
S. Purcell, S. Uthicke, J.-F. Hamel & A. Mercier, eds. Advances in sea cucumber aquaculture and
management. FAO, Rome. Fisheries Technical Paper No. 463, 425 pp.
KalininV.I., Anisimov M.M., Prokofiev N.G., Avilov S.A. Afiyatullov S.H. and Stonik V.A. 1996. Biological
activities and biological role of triterpene glycosides from holothuroids. Echinoderm Studies 5:139-181
Kinch J. 2002. Overview of the beche-de-mer fishery in Milne Bay Province, Papua New Guinea. Bechede-Mer Information Bulletin 17: 2-16.
Lambeth L. 2000. The subsistence use of Stichopus variegatus (now S. hermanni) in the Pacific Islands.
Beche-de-mer Information Bulletin 13: 18-21
Lovatelli A. , C. Conand, S. Purcell, S. Uthicke, J-F. Hamel & A. Mercier, eds. 2004. Advances in sea
cucumber aquaculture and management. FAO, Rome.Fisheries Technical Paper No. 463, 425 pp.
Martinez P.C. 2001. The Galapagos sea cucumber fishery: a risk or an opportunity for conservation? Bechede-Mer Information Bulletin 14: 22-23.
72
Mmbaga Twalibu K. and Yunus D. Mgaya 2004. Studies on sea cucumber in Tanzania and the gaps towards
resource inventory and management. In A. Lovatelli, C. Conand, S. Purcell, S. Uthicke, J.-F. Hamel & A.
Mercier, eds. Advances in sea cucumber aquaculture and management. FAO, Rome. Fisheries Technical
Paper No. 463, 425 pp.
Mercier A., Hidalgo R.Y and Hamel J-F. 2004. Aquaculture of the Galapagos sea cucumber Isostichopus
fuscus In A. Lovatelli, C. Conand, S. Purcell, S. Uthicke, J-F. Hamel & A. Mercier, eds. Advances in sea
cucumber aquaculture and management. FAO, Rome. Fisheries Technical Paper No. 463, 425 pp.
Polon P. 2004. The Papua New Guinea national Beche-de-mer fishery management plan. In A. Lovatelli,
C. Conand, S. Purcell, S. Uthicke, J.-F. Hamel & A. Mercier, eds. Advances in sea cucumber aquaculture
and management. FAO, Rome. Fisheries Technical Paper No. 463, 425 pp.
Preston GL 1993. Beche-de-mer. In: Nearshore Marine Resources of the South Pacific. Wright A & Hill L,
eds., pp. 371--407. Institute of Pacific Studies, Suva; Forum Fisheries Agency, Honiara; International
Centre for Ocean Development, Canada.
Rasolofonirina, R. and Conand C., 1998 - L’exploitation des holothuries dans le sud-ouest de Madagascar,
région de Toliara. Bêche-de-mer Information Bull., 10 : 10-13.
Rasolofonirina R. and Jangoux M.. 2004. Sea cucumber fishery and mariculture in Madagascar. A case study
of Toliara, south-west of Madagascar. In A. Lovatelli, C. Conand, S. Purcell, S. Uthicke, J.-F. Hamel & A.
Mercier, eds.. Advances in sea cucumber aquaculture and management. FAO, RomeFisheries Technical
Paper No. 463, 425 pp.
Sachithanantan K., 1972 - South Pacific Islands Bêche-de-mer fishery. F.A.O., Fi : DP. RAS, Rome, 69,
102.11 : 32 p.
Sant G. 2006. CITES and sea cucumbers. Document prepared for the workshop on Conservation of sea
cucumbers, Kuala Lumpur March 2004.
Sella A. and Sella M. 1940 - L'industria del trepang. Thalassia, 4, 1 : 116 p.
S.P.C 1990 to 2004. Beche-de-mer Information Bulletin 1 to 19. Secretariat of the Pacific Community
S.P.C. 1994. Sea cucumbers and beche-de-mer of the Tropical Pacific. Secretariat of the Pacific Community.
Handbook 18, 51 pp.
Rodriguez E. and S. Marques Pauls. 1998. Sea cucumber fisheries in Venezuela. Echinoderms san Francisco
Intern; Echinoderm Conference, Mooi and Telford (eds), Balkema, Rotterdam: 513-522
Tuwo A. 2004. Status on sea cucumber fisheries and farming in Indonesia. In A. Lovatelli, C. Conand, S.
Purcell, S. Uthicke, J.-F. Hamel & A. Mercier, eds. Advances in sea cucumber aquaculture and
management. FAO, Rome.Fisheries Technical Paper No. 463, 425 pp.
Verbist J.F. 1993. Pharmacological effects of compounds from Echinoderms. Echinoderm studies 4: 111-186
Yaqing C., Changqing Y. and Xin S. 2004. Sea cucumber (Apostichopus japonicus) pond polyculture in Dalian,
Liaoning province, China In A. Lovatelli, C. Conand, S. Purcell, S. Uthicke, J.-F. Hamel & A. Mercier,
eds. Advances in sea cucumber aquaculture and management. FAO, Rome.Fisheries Technical Paper
No. 463, 425 pp.
Zoutendick D. 1989. Beche-de-Mer. Rori of the Cook Islands. Report for the Ministry of marine Resources
Cook Islands, 6.
73
Management and Conservation Strategies
and Practices for Sea Cucumbers
Andrew Bruckner
NOAA Fisheries,U.S. Department of Commerce, USA
EXECUTIVE SUMMARY
This document presents a summary of current sea cucumber fishery practices and management options, with
discussion on opportunities for sustainable wild harvest, aquaculture, efforts to enhance wild populations and
trade controls. Sea cucumbers are both economically and ecologically valuable marine invertebrates, with a
growing international trade for food, medicinals, nutritional supplements, biomedical research, aquarium displays
and other uses. The greatest threat to sea cucumber resources is overfishing, primarily as a result of the present
fishery system, which usually involves foreign buyers offering a low price to indigenous fishermen for valuable
species. While indigenous fishermen may be concerned with sustainable resource utilization, buyers focus on
the largest profit in the shortest time period. As a result, fishermen initially target the largest individuals of the
high value species; once these are fished out, larger numbers of individuals of a smaller size are taken, along
with harvest of medium and low value species. Once an area is depleted, fishermen and buyers must look for
new sources.
Developing management strategies for an exploited fishery resource requires consideration of specific details
of the biology of the target species and their population dynamics, details on the fishery, processing and
marketing methods, and the social and economic context of the fishery. Alternative and complementary
conservation measures such as aquaculture and stock enhancement programs can help conserve and rebuild
wild populations. However, these measures also require considerable investment in research on life history
and ecological data, as well as information on optimal conditions for reproduction, settlement, growth and
release into the wild. Proposed or existing fishery management strategies have included minimum sizes, spatial
and temporal closures, rotational harvest, harvest or export quotas, gear restrictions and limited entry. While
each of these approaches can assist in sustainable management of the resources, they are likely to be most
effective when multiple strategies are combined under one plan, such as a minimum size and quota for each
target species along with establishment of protected areas. In developing countries, regional management plans
combining multiple fishery approaches and emphasizing adaptive management are likely to be most successful
at ensuring conservation and sustainable harvest, provided that the measures are adopted through consensus
with multiple stakeholders and local communities take on some of the responsibilities for management.
INTRODUCTION
Trends in Sea Cucumber Fisheries and Trade
The harvest of sea cucumbers for bêche-de-mer provides a valuable source of income for many coastal
communities in developing countries throughout the tropical and subtropical IndoPacific. Until recently, sea
cucumbers were harvested primarily at low subsistence levels through small scale artisanal fisheries, as access
was restricted due to smaller and fewer boats and certain gear types such as SCUBA and hookah were not
used. Many of these fisheries had been operating for up to 1000 years, with the particular species, product
type and use varying between islands (Conand, 2001). Since the 1980s, sea cucumber fisheries have been
characterized by boom and bust cycles, with a growing number of reports of over-harvesting as fishermen
74
attempt to supply an increasing demand for bêche-de-mer in Asian markets (Adams, 1992; Trinidad-Roa,
1987; Conand 2000; 2001; Ibarra and Soberon, 2002). Production from tropical holothurian fisheries increased
almost fivefold between 1985 and 1989, reaching an estimated worldwide trade of 9,000 metric tons (mt)
dried (Conand and Byrne, 1993). By 1995, exports of sea cucumbers to Chinese markets were approximately
13,000 mt, valued at over USD $60 million (Conand 1997; 1999). Recent trends in the export fishery include
increases in the number of producing countries and species in trade, and an expansion of fisheries in both
tropical and temperate regions into non-traditional fishing areas such as the Caribbean, eastern Pacific and
North America (Conand and Byrne, 1993; Ibarra and Soberon, 2002; Fiendel, 2002; Buitrago and Boada,
1996; Rodríguez and Marques-Pauls, 1998; Fuente-Betancourt et al. 2001). Statistics from one of the largest
importers show an increase from 25 source countries in 1987-1989 to 49 countries in 2000-2001 (Hong
Kong Special Administrative Region data). In addition to a growing international trade of bêche-de-mer,
additional species are being harvested for aquarium organisms, biomedical research, pharmaceuticals, traditional
medicines, nutritional supplements and plant fertilizer (Beumer, 1992; Baine and Sze, 1999; Chen, 2003).
Recent Status of Sea Cucumber Fisheries and Target Stocks
The rapid decline of sea cucumber populations worldwide has triggered fluctuations in market prices, rapid
expansion and spread of fisheries, severe overfishing, and poaching by nationals and foreign fishermen (Conand,
1999; Kinch, 2002; Jun, 2002; Conand, 2001). During the 1980s and 1990s, increased commercial harvesting
and export of sea cucumbers stimulated financial gains for fishermen and local communities that process the
meat, but the benefits to any one fishing community are typically short-lasting (Kinch, 2002). In at least 10
countries, catch per unit effort for high value species declined shortly after fisheries became established, forcing
a shift in fishing effort to smaller individuals and lower value species [e.g., Australia (Uthicke and Benzie,
2000); Fiji (Adams, 1992); India (Nithyanandan, 2003); Indonesia (Moore, 1998); Madagascar (Jangoux et
al., 2001); Malaysia (Baine and Choo, 1999); New Caledonia (Conand and Byrne, 1993); Papua New
Guinea (Kinch, 2002); Philippines (Trinidad-Roa, 1987); and Solomon Islands (Holland, 1994)]. Sea cucumber
fisheries were historically managed by local communities or through tenurial systems. In more modern times,
commercial fisheries have often been poorly managed, with management measures applied in response to
dwindling stocks. For example, commercial harvest in most developing countries initially begins as an open
access fisheries, with a subsequent closure or relocation of the fishery within a few years due to overexploitation
(Castro, 1995; Lokani, 1996; Trianni, 2002).
The marked increase in landings and export of holothurians in combination with few existing management
measures, as well as limited fisheries, trade, biological and population data for commercially important species,
are key factors contributing to the decline and extirpation of holothurian populations (Conand and Byrne,
1993). Certain aspects of sea cucumber life history and ecology such as a late maturity and ease of collection
renders them highly susceptible to over-exploitation, and may result in recruitment failure with prolonged
recovery times (Richmond, 1996). It is now apparent that certain populations of high value sea cucumbers like
the sandfish (Holothuria scabra) have been exploited so heavily in some Pacific Islands that it will take decades
for stocks to recover in absence of adaptive management measures (Preston, 1993; Kinch, 2002).
Purpose of this Document
This document has been prepared by NOAA Fisheries for a technical workshop that will be convened by the
CITES Secretariat in Kula Lumpar, Malaysia from 1-5 March, 2004. The purpose of the workshop is to
develop conservation priorities and actions to secure the conservation status of sea cucumbers, addressing
trade monitoring and controls, national legislation, f isheries management provisions, other conservation
75
approaches, enforcement, and capacity building. This document summarizes current sea cucumber fisheries
practices, management options and conservation practices applied both domestically and regionally, including
opportunities for sustainable wild harvest, aquaculture, and efforts to enhance wild populations. The benefits
and drawbacks of these measures and their contribution to the recovery of overfished stocks are evaluated.
Brief descriptions of sea cucumber fisheries are provided for each of the major exporting countries, as well as
possible adaptive management approaches that have been recommended and/or implemented to reduce pressure
on depleted stocks or promote sustainable harvest.
CURRENT SEA CUCUMBER FISHERIES PRACTICES
Holothurian fisheries are based on about 30 of the over 1000 existing species, with most utilized as a raw,
frozen, salted or dried product for human consumption (e.g., bêche-de-mer; trepang); numerous additional
species are harvested at a much lower volume for aquarium displays, biomedical research, dietary supplements
and other uses (Conand, 1993; Baine and Sze, 1999; Chen, 2003; Conand, 2001). Tropical and subtropical
fisheries in the western Pacific are multi-species as compared to tropical fisheries in the Indian Ocean (H.
scabra), eastern Pacific (Isostichopus fuscus) and Caribbean (Isostichopus badionotus, Holothuria mexicana
and Astichopus multifidus). In the western Pacific, fisheries primarily target shallow water (up to 50 m depth)
deposit-feeding holothurians belonging to two families and eight genera: Actinopyga, Bohadschia, Microthele
and Holothuria (Holothuridae) and Isostichopus, Parastichopus, Stichopus and Thelenota (Stichopodidae).
The more recent temperate water fisheries are each based on one or two species that are found in the western
Pacific around Japan, Korea and Russia (S. japonicus), southern hemisphere off New Zealand (S. mollis),
eastern Pacific coast of North America (P. californicus and P. parvimensis) and western Atlantic coast of
North America (Cucumaria frondosa).
Holothurians that are targeted by bêche-de-mer fisheries range in size from about 5 cm to over 1 m in length,
while aquarium specimens are typically smaller (2-20 cm). Bêche-de-mer species may be classified into three
categories of commercial importance based on their abundance, appearance, odor and color, thickness and
quality of body wall, and main market demand and value (Conand, 1993). Worldwide, the single most
important species by volume is the temperate holothurian, S. japonicus, with over 12,000 mt consumed in
Japan and Korea in 1983 (McElroy, 1990). However, the total landings of S. japonicus in Japan declined
from 25,000 mt in 1983 to 7000 mt in 1995, while the volume of tropical sea cucumbers in trade has grown
considerably (Conand, 1986; McElroy, 1990; Ito and Kitamura, 1998). Currently, the species of highest
commercial value are H. fuscogilva (white teatfish), H. nobilis (black teatfish) and H. scabra (sandfish),
worth US$15-40/kg on the Asian market in 2002, with bigger specimens fetching a higher price per kilogram
than smaller specimens (Infofish trade news, 2002). Species of medium value include A. echinites (brownfish),
A. miliaris (blackfish) and T. ananas (prickly redfish) (USD $10-12/kg). Species of low value include B.
marmorata, H. atra, H. fuscopunctata, S. chloronotus and S. variegates (USD $2-10/kg). Most other
tropical and temperate species are medium to low value.
Fishermen may operate from shore, or out of small boats (dugout canoes, sailing boats, motor boats) fitted
with SCUBA, a hookah system or trawl gear. For instance, in Papua New Guinea, small, motorized banana
boats and outrigger canoes with sails and outboards are used to access sites, but most collection is done by
walking on the reef flat at low tide and snorkeling while hand collecting (Lokani et al., 1996). In British
Columbia, geoduck and urchin dive fishermen target sea cucumbers to supplement their operations; boats are
22 foot skiffs to 40 foot salmon boats converted for diving, with 2-3 divers and one tender per boat (Muse,
1998). In tropical countries, the sea cucumber fishery is often one part of a multi-species fishery for reef fishes,
corals, and other invertebrates. In remote tropical areas, vessels may remain at sea for several weeks.
76
Fishing gear and methods for sea cucumber fisheries include:
• Small bottom trawls (roller pulling nets, beam trawl nets, scallop-drag gear etc.) used primarily in soft
bottom habitats away from reef structures;
• Direct collection by hand (reef flat gleaning at low tide or wading) or collection with spears, hooks and
scoop nets in shallow-water mangrove lagoons, reef flats and grass beds;
• Collection by hand using snorkel and diving gear (SCUBA and hookah) and lift bags for deeper reef
and lagoonal environments; and
• Collection at night with SCUBA, snorkeling or wading using underwater lights or torches.
MEASURES TO ENSURE SUSTAINABLE OR ENHANCED SEA CUCUMBER FISHERIES
Possible approaches to ensure sustainable sea cucumber fisheries include:
1) Aquaculture and mariculture to provide an alternative source of bêche-de-mer;
2) Reseeding and relocation of juveniles/adults to rehabilitate degraded areas and enhance wild stocks;
3) National controls on harvest or export, including a CITES Appendix III listing (Ecuador) or placement of
overharvested species on National endangered or threatened species lists, with prohibitions on take or
export (India, Mexico);
4) Specific domestic fishery management strategies to conserve wild populations while allowing sustainable
harvest.
5) Regional management approaches and cooperation in resource harvesting and marketing by multiple
stakeholders and resource management agencies; and
6) International controls on exports such as a possible CITES Appendix II listings for one or more species.
Aquaculture and Mariculture
Sea cucumber farming practices have greatly expanded over the last five years, with programs underway in
China, Indonesia, Vietnam, Marshall Islands, Japan, Maldives, New Zealand, India and other countries. Aspects
of the development of sea cucumber larvae are described for a number of commercially important species, and
researchers are successful at inducing spawning, gamete fertilization and early larval rearing for several of these
(Conand, 1993; Ito, 1995; Ramofafia et al., 1995; Morgan, 2000; Pitt, 2001). Broodstock can be collected
from the wild and induced to spawn in captivity. In addition, several high-value species have been reported to
reproduce asexually by fission and induced fission is being examined as a potential technique to propagate
commercially important species (Reichenbach et al., 1998). For many species reliable feeding regimes for sea
cucumber larvae through the planktonic part of their life cycle to settlement have been developed (Purcell et al.,
2002). One, temperate species (A. japonicus) can be produced successfully in large commercial quantities.
The rapid expansion and intensification of sea cucumber farming has led to the occurrence of various diseases,
causing economic losses and becoming one of the limiting factors in the sustainable development of the industry
(Yin-Geng et al., 2003). while Aquaculture of tropical sea cucumbers has been more challenging due to can be
difficulties in to holding adults in in captivity, and reduced feeding, weight loss and poor gonadal development
has been reported (Battaglene, 1999). Currently, most effort in the tropics is geared towards H. scabra.
Some of the recent successful sea cucumber farming venturesculturing efforts include:
•
The Sea Farming Center in southern Japan that can produce up to 1 million juveniles per year (Ito and
Kitamura, 1998).
77
Table 1. Information needed to develop sustainable management plans for sea cucumber
fisheries.
Information
Requirement
Taxonomy
Distribution
Habitat
Stock
structure
Reproduction
Recruitment
Growth
Natural
mortality
Fishing
mortality
Density
dependence
Description
Methods
Unambiguous identification of species
Morphological, microscopical
(spicule analyses) & molecular
analyses; photographic keys for
live and dried specimens.
Museum specimens, fisheriesdependent & fisheriesindependent surveys
Extent of species occurrence within- and
between-countries
Spatial structure of populations
(clumped or uniform)
Habitat requirements and preferences;
effects of habitat type (e.g., soft
sediment, grassbed, cobble) on growth,
reproduction and survival
Single or multiple stocks
Standing stock (size, biomass)
Exchange of individuals among stocks
Number, timing and season of broadcast
spawning events
Age- & size-specific fecundity
Age & size at first reproduction
Duration of larval existence;
Dispersal of larvae and juveniles;
Settlement cues (physical, chemical or
biological)
Age-specific growth rates
Seasonal growth rates
Relationship between environmental
attributes and growth
Age-specific mortality rates
Size-specific mortality rates
Size of fishing fleet
Spatial and temporal distribution of
fishing effort
Size-specific fishing mortality
Sex-specific fishing mortality
Compensatory or dispensatory (?)
reproductive output (including Allee
effects); Density-dependent growth
(resource limitation)
78
Remote sensing and in situ
mapping and habitat
characterization; fisheriesdependent & fisheriesindependent surveys; broadbased underwater censuses,
physio-chemical measurements
Genetics, tagging, habitat
surveys, fisheries-independent
surveys
Fisheries-dependent & fisheriesindependent surveys, laboratory
studies, tagging and underwater
studies
Tagging, genetic analyses,
ecological surveys
Tagging, cohort analysis
Fisheries-independent surveys,
life-table analysis
Logbooks, fisheries-dependent
surveys, fisheries observers,
catch sampling
Fisheries-independent surveys,
meta-analyses from multiple
populations and years
Table 2. Management approaches to enhance sustainability of sea cucumber fisheries.
Approach
Description
Benefits
Seasonal
closure
Fishery closure during
breeding season
Spatial
closure
Fishery closure in sensitive
areas or in areas that are
depleted
Rotational
closure
Rotate between participating
islands; divide collection areas
into sections, each open to
harvest during a certain time
period on a rotational basis.
Fishery closed at night.
Enhance recruitment of stocks; one problem is
that some species reproduce from Nov-Jan while
others peak between June-July.
Can include establishment of no-take areas which
may help in the recruitment of stocks to fished
areas and zoning for multiple uses which may
reduce conflicts among different user groups.
This will reduce pressure in one area and allow a
fished site to recover. Allows countries to pool
resources and obtain minimum needed for export
without destroying resources in one area.
Temporal
closure
Quotas
Minimum
size
Maximum
size
Gear
restrictions
Gear
restrictions
Limited
entry
Logbooks
Species-specific total
allowable catch for each
location; total closures for
certain species with low
abundance.
No take until species have
reached reproductive maturity.
Take of juvenile species for
mariculture grow-out,
aquarium organisms, and other
uses.
Limitations on use of trawls
Prohibitions on use of SCUBA
or hookah.
Limitations on amount of
effort based on a licensing or
permitting system; restrict
entry to locals or nationals.
Information on catch location,
species composition, method
of collection, quantity and
Certain species such as H. scabra emerge at night
and would be easily overexploited at night.
Avoid declines in CPUE masked by shifts in
fishing effort to other less valuable species; ensure
that the total depletion of high value species does
not occur.
Biological justification: maximize yield per
recruit; allows individuals to reach reproductive
maturity and spawn at least once before harvest.
Economic justification: bigger specimens
commend a higher price than smaller specimens
Drawback: animals can change size and shape
dramatically once caught; at least one species
(curryfish) fetches a higher price at a smaller size.
Harvest of juveniles at a vulnerable stage in their
development may provide a source for individuals
for commercial grow-out with minimal
implications to wild populations.
Reduce bycatch and habitat destruction.
Provides a refuge for part of the population (depth).
Improves compliance with management measures.
Ensures that profits from fishery benefit local
community. Assigning territorial rights to fishing
coops may reduce problems associated with
uncontrolled open-access fishing.
Facilitate acquisition of more reliable fishery
dependent data for use in management; increase
compliance with management measures.
79
•
•
•
•
•
•
•
•
China is is one of the first locations to successfully raise A. japonicus sea cucumbers on a large
commercial scale in ponds and enclosures at sea. For instance, Chen (2003) , with reports of production
of about 1000 mt of A. japonicus each year, and 1025 mt of several other species in another location
during 2001. (Chen, 2003). Total landings of A. japonicus from farms in Liaoning and Shandong
Provinces is reported to have exceeded 5,800 mt in 2000 (Jiaxin, 2003). In addition, in the Dalian
area more than 2000 hectares of ponds are being used for polyculture of shrimp and sea cucumbers
(Yaqing et al., 2003)
A sea cucumber ranching operation was established on an atoll in the Maldives involving H. scabra
from India, a species that is not native to this area. In less than one year, juveniles have grown to 15 cm
and are being harvested for export.
Collection of small (juvenile) sandfish (H. scabra) from the wild for grow out in ponds and pens has
been reported from India, Indonesia and Vietnam (Pitt, 2001).
India is able to produce larvae and juveniles of H. scabra from wild brood stock, which are produced
in a hatchery, and are grown out in cages and pens on the sea floor in several Bays and harbours, and
also in shrimp ponds in polyculture (James, 2003)
Madagascar established a sea cucumber hatchery in 2000 that can now produce juveniles (1-2 cm) of
H. scabra, and a sea cucumber grow-out farm has been established (Jangoux et al., 2001).
Indonesia has developed sea cucumber farms in four areas with substantial production, including
Papua (378 mt), Central Sulawesi (200 mt), southeast Sulawesi (3 mt) and East Kalimantan (1 mt);
some of the production is actually wild harvested juveniles that are grown to market size in cages or
ponds (Tuwo, 2003).
The possibility of usingIn several countries commercial shrimp farming ponds are being used for grow
out of sea cucumbers is being explored, as holothurians ingest large amounts of sediment and may
improve water conditions by removing organic debris. Preliminary experiments show high survivorship
and rapid rates of growth until the wet season, when salinities fluctuate andnd mass mortalities may
occur (Pitt, 2001; Chen, 2003).
Rearing of Isostichopus on land and in abandoned shrimp ponds is underway in Ecaudor, with 30-50%
survival of larvae and rapid growth (8 cm in 3.5 months) (Mercier et al., 2003).
Restocking
The release of juvenile sea cucumbers produced in hatcheries is thought to be one way of rebuilding wild
stocks (e.g., “restocking” or “reseeding”) to the point where they can sustain regular harvest. There is also the
potential to increase harvests beyond historical levels by releasing sufficient cultured juveniles into the wild to
reach the carrying capacity of the habitat and overcoming recruitment limitations (e.g., “stock enhancement”)
(Munro and Bell, 1997; Battaglene and Bell, 1999). Relocation of recruits and juveniles from areas of high
abundance to depleted areas as a form of sea ranching has also been recommended, but not attempted on a
large experimental scale. In addition, artificially aggregating adults is also another option to enhance stocks.
These approaches may be beneficial in areas where populations of certain species have been reduced to such
low levels by fishing that remaining individuals are incapable of successful reproduction due to Allee effects, or
when recruitment is be limited due to a) certain physio-chemical properties of the site (e.g., water circulation
patterns); or b) the larvae of target species have limited dispersal capabilities. However, there are numerous
concerns associated with reintroduction of hatchery produced species, including possible genetic considerations
and disease introductions.
Holothuria scabra appears to be the tropical holothurian most suited to restocking in the western Pacific and
Southeast Asia; however, it has not been demonstrated that farm-raised juveniles will survive in the wild and
80
information is lacking on optimal release strategies (Pitt, 2001). Research in restocking and stock enhancement of tropical sea cucumbers is being undertaken or has been proposed in Ecuador, Philippines, India,
Kiribati, Maldives, Marshall Islands and the Solomon Islands (Battaglene and Bell, 1999).
•
Some of the earliest restocking experiments were attempted in Japan. In one area, 1,700 juveniles
were released and fishing was closed for two years to allow these to mature. At the end of the
prohibition, the 90 fishing boats that targeted this area had an estimated total catch that was 30 X
higher than previous catches in this area (Arakawa, 1990). More recently, 11 farming centers released
2,557,000 juvenile sea cucumbers (9 mm) in 1995 (Ito, 1995); it is unclear whether follow-up studies
were conducted to determine what proportion of these survived.
•
International Center for Living Aquatic Resources Management (ICLARM) has been examining the
potential for releasing cultured juveniles of H. scabra and A. mauritiana in the Solomon Islands as a
means of restoring and enhancing tropical sea cucumber stocks (Battaglene, 1999). ICLARM produced over 200,000 juveniles from six spawning events in the mid-1990s. In 2000, they released
2600 juveniles in the Western Province in areas where spawning adults were found; survival rates are
unknown (Battaglene, 2000).
•
In preliminary trials from the Solomon Islands, 15-90% of the hatchery bred animals released in sea
grass sites were missing after 24 hours (Dance et al., 2000). In a second trial, juveniles were released
in sand or silt reef flat, mangrove and seagrass sites, with the highest short-term survival at mangrove
sea grass sites and high rates of predation occurring in reef environments (Dance et al., 2000).
• A sea cucumber project in New Caledonia aims to determine the best strategies for releasing into the
wild the sandfish (Holothuria scabra), for purposes of restocking and stock enhancement of inshore
fisheries. The sandfish have beenwill be cultured from local broodstock and have shown high survival
and growth in certain habitat types. Transportation methods and the sizes, densities, habitats, times of
the day and year for release will be optimized by tracking the fates of juveniles at inshore sites in the
Provinces of New Caledonia (Purcell, Gardner and Bell, 2003).
•
In Suez Canal University, the release of cultured juveniles of A. mauritiana on the red Sea coast is
being explored to restore depleted populations and possible enhancement of fisheries (Gabr et al.,
2003).
CONSERVATION PRACTICES AND STRATEGIES
While sea cucumber fisheries remain unregulated in most developing countries, other developing and developed
countries have established measures to manage and conserve holothurian resources, in an attempt to prevent
over-harvesting (Table 4, 5; Appendix I). In most countries with open-access sea cucumber fisheries, fisheries
have passed through four phases, inevitably leading to overfishing (Ibarra and Soberon, 2002). Fishermen first
target dense populations with easy access, especially nearshore, shallow environments; stocks are initially
underexploited, but the catch keeps on growing as effort increases and the industry flourishes. As the industry
matures, the level of capture becomes constant, but more fishing effort is needed to achieve these levels. As all
of the suitable species and size classes are removed from one area, the distribution of fishing effort expands to
more remote areas and deeper environments. This practice may result in extensive areas that are essentially
free of harvesting pressure, but it also leads to the localized depletion of stocks where fishing has occurred.
81
Development of sustainable management approaches for sea cucumber fisheries are not easy, and current
management tools like size limits, gear restrictions, spatial and temporal closures, quotas and marine reserves
have not been very effective in managing large commercial export fisheries in tropical regions (Preston, 1993;
Dalzell et al., 1996). Part of the problem is that developing countries do not have the human resources to
collect data on the biology, ecology and population dynamics of sea cucumbers necessary to develop adaptive
management plans, or the capacity to enforce regulations. The multi-species nature of most tropical sea
cucumber fisheries, as well as the remote and artisanal nature of these fisheries, makes it difficult to obtain data
needed to manage sea cucumber fisheries.
Traditional Management and Tenurial Arrangements
Traditional, tenure or community-based management approaches were highly successful in Pacific islands and
other areas when holothurians were harvested at much lower levels only for traditional and subsistence uses.
These approaches are less effective now, since:
1) some of the traditional cultures are being lost;
2) population growth and increasing international demand places greater pressure on the resources;
3) sea cucumbers populations are being targeted that were not traditionally exploited, due to availability of
motorized boats, SCUBA and hookah gear which allows fishers to reach distant and deepwater habitats;
and
4) non-local collectors are fishing in many areas, and poaching and illegal trade has increased (Samyn, 2000).
Regional Management Approaches
When developing management plans for sea cucumber fisheries, the target species in some locations should be
considered as transboundary stocks. Management of these stocks plans requires bilateral and international
agreements targeted at protection of reef habitats, spawning aggregation areas and parental stocks. Although
adult sea cucumbers are relatively sedentary, fertilized eggs and developing larvae may disperse away from the
natal reef. If larvae are widely dispersed, managing an adult population of sea cucumbers may not guarantee
a healthy stock if that managed population depends on an upstream source of larvae for replenishment. This is
particularly relevant in the Indo-Pacific where larval dispersion may occur across international borders, separating
healthy and overexploited reef systems. Conversely, if larvae are locally retained, local management will have
local consequences. In these situations, poor ecosystem and fisheries management may cause declining stocks,
but good management will lead to local recovery of fished populations and sustainable fisheries.
To date, only Papua New Guinea and Australia have initiated a regional management approach for the Torres
Strait Fishery. They have ratified the Torres Strait Treaty, which includes provisions for joint management and
cooperation in surveillance activities (Lokani et al., 1996).
There has also been a recent resurgence of interest in community involvement and participation in all aspects of
marine resource management and monitoring. One approach involves collaborative efforts between industry,
resource management agencies, local communities and non-governmental conservation and sustainable
management organizations.As an alternative approach, communities have taken on the responsibility for managing
their resources, with the government providing limited support and infrastructure. Examples include:
82
•
Development of an association of licensed exporters in Fiji (Bêche-de-mer Exporter’s Association) to
maintain quality standards and provide the Fiji government data on the fishery (Preston, 1990).
• While the Fisheries Division in Fiji has no authority to set up no-take reserves, the Fisheries Act allows
resource custodians to endorse fishing permits and to ban fishing for a particular species in an area
under their control (Adams, 1992).
• Sea cucumber fishermen from a village in Sulawesi near the Wakatobi Marine National Park have
agreed to avoid harvesting juveniles (Moore, 1998).
•
Shared management was introduced in Madagascar in 1998, with partnership between the Madagascar
National Trepang traders group and the government resource managers.
National Conservation Measures
Several countries have adopted conservation measures to prevent illegal fishing and export, and to recover
depleted sea cucumber stocks. These include:
•
The Ecuadorian government requested international assistance in preventing illegal exports and adopted
a CITES Appendix III listing in 2003.
•
India added all sea cucumbers to Schedule I list of the Wildlife Protection Act in 2001, with a prohibition
on exports.
•
Mexico declared I. fuscus in danger of extinction in May of 1994; the species was placed on a
“species under special protection” list in March 2000.
MEASURES IN FISHERIES COUNTRIES TO CONTROL OR MONITOR HARVEST AND
TRADE AND TO PROTECT OR ENHANCE STOCKS
The management goal for sea cucumber fisheries is to preserve, protect, and perpetuate sea cucumber resources;
provide for their sustainable harvest; protect the habitat necessary to sustain these harvests; and minimize bycatch mortalities of other species. For effective conservation, a sea cucumber fishery must conserve target
stocks, sustain marine ecosystems and non-target species, and also provide economic and social benefits
consistent with the goals and desires of coastal communities. Domestic management options include a number
of tools that have been applied to manage tropical and temperate fisheries, summarized under input controls
(restrictions on fishing effort) and output controls (restrictions on sea cucumbers that can be retained by the
fishery) (Table 2, 4 and 5; Appendix I).
I nput Controls
Fisheries closures: Sea cucumber fishery closures include prohibitions on the take of certain species, or entire
closures of the fishery. Entire fisheries (e.g., Venezuela, Ecuador) or certain sites (e.g., Mexico, Panama) have
been closed to harvest a short time after the fishery commenced, due to rapid overexploitation and biological
or commercial extirpations of target species (Castro, 1995; Rodríguez and Marques-Pauls, 1997; Guzman
and Guevara, 2002). In other locations, the take of certain species is now prohibited due to their rarity. This
83
Table 3. Other tools, approaches, and information needs that contribute to the development
of sustainable management plans for sea cucumbers.
Approach
Description
Benefits
Baseline surveys
and monitoring
Baseline surveys and
monitoring of Population
abundance estimates including
abundance and diversity in
areas under exploitation and
control areas.
Fishery-dependent
data
Monitoring of catch data
(numbers of individuals
harvested, sizes, dates and
location of collection) and
trade.
Development of associations
of licensed fishers and
exporters in partnership with
local communities and national
resource management
agencies.
Field data necessary to determine
sustainable harvest guidelines including
which sites are feasible for harvest and to
set their quotas; establish permanent
surveys sites to monitor harvest pressure,
recovery from harvest and seasonal
variation in recruitment.
Fishery dependent data necessary to feed
into development of management plan and
subsequent adaptive management
measures.
Industry/
community
associations
Training in
processing
Sea cucumber
research
Aquaculture/
mariculture
Sea ranching
operations
Restocking
programs
Multi-stakeholder decision making
process increases likelihood of success:
Improve understanding of conservation
and management needs; facilitate
enforcement of community-adopted
management measures; provide training
and reporting of catch and export data;
contribute to resource assessments.
Improve skills of sea cucumber A proportion of the catch is rejected due
processors to minimize
to decomposition caused by incomplete
wastage.
drying and improper storage.
Research programs on
Provide information needed on life
taxonomy, biology and
history, population connectivity, habitat
ecology, including growth,
requirements etc. than can feed into
length and weight analyses;
management actions.
reproductive biology; and
genetics.
Spawning, growth and
Reduce demand on wild populations;
settlement of larvae; raise
grow-out may be preferable for curryfish,
juveniles to commercial size.
which fetches a higher price at a smaller
size and can be grown to market size
faster.
Grow-out of farm raised
May reduce demand on wild populations.
juveniles or juveniles removed Effect of harvest on juveniles unknown.
from wild.
Release of farm-raised
Recover extirpated stocks; Increase yield
juveniles.
of fishery.
84
includes bans on the harvest or export of three of the most widespread and highest value species, including H.
scabra (Fiji, PNG), H. atra and H. nobilis (parts of Australia). In India, all sea cucumbers were placed on
Schedule I list of the Wildlife Protection Act (1992) in 2001, and their collection was strictly banned. This was
a conservation step taken by the government of India to revive depleted stocks, but illegal fishing pressure has
persisted and field monitoring studies indicate low biomass of target species with little or no recovery
(Nithyanandan, 2003).
While a closure may be necessary to prevent extirpations or to rebuild depleted stocks, there are few social or
economic benefits of this approach, as it is likely to lead to illegal fishing and export and substantial loss of
revenue for fishermen.
Gear Restrictions: The most common gear restrictions for sea cucumber fisheries include prohibitions on
the use of SCUBA, hookah and other types of underwater breathing apparatus; restrictions on locations that
can be trawled; and limitations on the size and shape of trawl gear. Restricting collection to free-diving,
wading, and reef flat gleaning (ban on SCUBA or hookah) would limit the amount of time available to search
for animals hidden away in the coral reef and it would prevent most fishing below 30 m. This is a conservative
method that should reduce recruitment overfishing because up to half the stock of some species live at depths
greater than 30 m (Preston and Lokani, 1990). In New Caledonia, black and grey color morphs of sandfish
occur in different habitats, with black primarily found in deeper water. Genetic studies indicated that both
populations were closely linked, suggesting that deep populations can constitute a buffer and a source of new
recruits to the fished shallow zones, as long as trawl or dive fisheries are prohibited in these areas (Uthicke and
Benzie, 1999). While a ban on the use of underwater breathing gear may protect a critical portion of the
population of species such as white teatfish and prickly redfish that have a wide depth distribution, other high
value species have a relatively shallow distribution and are unlikely to benefit from this measure (Lokani et al.,
1996).
Spatial closures: Spatial closures that have been used to protect sea cucumber populations include limits on
the depth of collection, closure of specific locations, and closure of a certain percentage of the coastline. The
establishment of no-take protected areas or other types of marine reserves and sanctuaries can benefit sea
cucumber fisheries by protecting a portion of the spawning stock that may provide recruits to replenish fishing
grounds, and by enhancing catches in adjacent, fished areas through emigration of juveniles or adults. Marine
reserves offer benefits to both fishery and non-fishery interests, but these are likely to be successful only when
developed in consensus with local communities and user groups, and when properly enforced. Other factors
fundamental to the design of effective sanctuaries include size, shape, and number of protected areas; habitat
types included; the life histories of the target species; the location of protected areas relative to currents that
may disperse larvae; and, the type of activities that are allowed.
A recent study from Australia found that the protection of whole reefs from fishing is an effective management
tool for the conservation of sea cucumbers, while the division of a reef into a fished and unfished zone is only
effective when protected areas are large or there is considerable genetic exchange among sites (Uthicke and
Benzie, 2000). In Australia, H. nobilis populations were found to have high gene flow, suggesting that recruits
can be received from a wide geographical area and stocks could be managed on a regional scale. In contrast,
separate genetic stocks of H. scabra were detected, which implies limited recruitment within regions that may
reduce the potential for recovery of overfished areas. Thus, H. scabra needs to be managed as separate
stocks and local refugia adjacent to collection sites must be established that have breeding populations of this
species (Uthicke and Benzie, 2001).
85
Seasonal closures or rotational harvest areas: Temporal closures are generally timed to protect certain
life history stages of a population or certain critical periods in their life, such as the time of spawning, and may
also be applied to maximize the quality of the product. Often referred to as “pulse fishing”, rotational harvest
typically involves harvesting a stock heavily, letting it lie fallow for a few years, and then harvesting it heavily
again. Seasonal closures and rotational harvest areas are effective strategies to control effort and limit yield in
one particular area to sustainable levels.
The main benefit of rotational harvest is that there would be an accumulation of individuals during the closed
period, with many growing to larger sizes, increasing their value in the marketplace. One concern is that each
time the closure is lifted, the removal of all or most of the spawning stock occurs. Thus, all new recruits must
come from elsewhere, unless the closure is left in place for a sufficient period to allow self-seeding. Another
disadvantage is that fishermen cannot fish in those areas during the closed years, and other sites must be
available to provide continuing employment. One way to address this involves designing a system where
different island states rotate harvest closures among species and countries, so that when the harvest is closed
in one area, it would be open in others.
Limited entry: Limited entry typically involves some form of licensing or permitting to restrict the number of
fishermen or the number of vessels. Restricted access to a fishery resource can reduce competition among
fishermen, help ensure long term economic and social viability and promote conservation among fishery
participants by giving those in the fishery a greater stake in the resource. It may also assist in obtaining data on
the fishery necessary for management, as most licensing schemes typically involve a requirement of logbook
submissions detailing location and amount of catch and other fishery-dependent statistics. This approach
appears to work well in developed countries, including the U.S. and Australia, where other alternative sources
of income are available for displaced sea cucumber fishers. In the U.S., licenses are given only to those
fishermen that landed a certain volume of sea cucumber in previous years. However, limited entry may not be
favored in developing countries, as it may have negative social effects. By reducing take or by limiting the
number of fishermen or vessels, certain fishermen or communities dependent on these resources for their
livelihood may become unemployed, with few alternative sources of income.
Output Controls
Quotas: A quota is a set limit on the amount of resource that can be harvested or exported during any year or
fishing season. Quotas are usually established to achieve a desired level of harvest, such that maximum sustainable
yield will not be exceeded. Quotas for sea cucumber fisheries have included total allowable catch for the
fishery overall, specific quotas for individual species, or quotas for specific areas. To be effective,
a desired maximum catch must be established and continuous monitoring of the catch must occur to determine
when the quota is reached. When the quota limit is reached, harvesting must cease until the next fishing year.
Management by total harvest quotas (e.g., "sea cucumbers ") versus managing for individual species may be
problematic because of the patchy spatial component of the fishery and holothurian populations, and the
possibility that the high value species will continue to be fished until stocks are extirpated. Another disadvantage
of using a quota is that a substantial amount of data on the fishery and the resource is necessary to determine
maximum sustainable yield. There are several approaches to determining maximum sustainable yield including:
86
•
Application of data on total catch and fishing effort over a number of years, with the maximum catch
per unit effort providing an estimate of the maximum sustainable yield (Richmond, 1996). In a typical
scenario, when a bêche-de-mer fishery is first established, the total catch increases as harvesting effort
increases. Some maximum level of harvest is rapidly reached at which time additional fishing effort
becomes less and less effective, and ultimately catch declines. The point at which catch per unit effort
is maximized would be equivalent to MSY. This scenario may not work for multi-species fisheries,
however. As one species is depleted, fishing effort shifts to less valuable species, but the total CPUE
for the "sea cucumber" fishery may actually increase, giving a false sense of security. There is also the
danger that fisheries targeting more abundant species can support continued fishing pressure on rare,
but extremely valuable, species. Thus, the management presumption that a fishery will become economically extinct before it is biologically extinct is not necessarily true. The most effective quota system
would involve dividing a location into harvest areas, each with its own quota developed for each target
species.
•
MSY can be estimated from biological parameters of the harvested stock, such as growth rates,
natural and fishing mortality rates, stock size and recruitment rates. This requires data on size and age
structure of populations and patterns of growth, which is not be available in most areas.
•
MSY can also be estimated more simplistically by 1) estimating the size of the harvested stock; 2)
determining the average age of individuals in the exploitable size classes; and 3) set an annual harvest
quota at a value equal to the stock size divided by its age. For example, if the harvestable portion of the
stock is 10 years old and you take 10% of the population each year, 10 years later the stock would
have rebuilt itself to the original condition (Richmond, 1996).
When a quota is used to manage sea cucumber fisheries, it is important that this quota is reevaluated frequently,
as new information becomes available, so any necessary adjustments can be made to prevent overexploitation.
Minimum sizes: Minimum sizes are typically based on the size at first sexual maturity, to ensure that the stock
does not crash because of recruitment failure. There are numerous benefits to delaying harvest until a species
has reached some minimum size, including the contribution of an individual to the population before its removal
and a higher market value typically associated with larger individuals. Large female sea cucumbers typically
produce more eggs than small females, there by contributing more to the abundance of future generations
(Richmond, 1996). Blanket size limits on all bêche-de-mer species has been suggested as one of the mechanisms
to prevent growth overfishing, but this is impractical because the size at sexual maturity established size
requirement. Nevertheless, a number of countries such as Australia, Papua New Guinea, Fiji, and Tonga have
recommended or adopted separate size limits for each species (Table 7; Appendix I). The advantage of using
minimum size for managing an export fishery is that enforcement can be done at the market place, avoiding the
need to intercept harvesters while fishing. Since the price of sea cucumbers is based on size, cucumbers have
to be weighed at the market already, providing an opportunity to detect undersized animals.
The disadvantage of this approach is that rejected undersized animals are already dead, and they represent a
loss to the reproductive capacity of the stock as well as economic loss to the fishermen (Richmond, 1996).
Another disadvantage of using minimum sizes is that this method does not guarantee that the maximum sustainable
yield will be harvested, and it does not predict how many sea cucumbers will be harvested. In fisheries
managed solely by minimum size, the harvest will be large in initial years, as all the individuals larger than the
minimum size will be subject to harvest. Over time, the largest individuals will become scarce, and annual
fishery will depend on how many animals grow to legal size in a year. However, determining size at reproductive
87
Table 4. Examples of existing regulations for sea cucumber fisheries in temperate waters.
THQ= Total harvest quota; HAQ=Harvest area quota; mt= metric tons.
Location and
species
Alaska,
USA
Open
Season
OctMarch
Harvest Area
Gear type
Quota
13 Fishery Management
units (FMU).
Max harvest
for each
fisher and
each FMU.
Washington,
USA
All year
5 management areas;
Rotation of harvest with
3.5 yr closure after 6
month fishing period.
SCUBA, Surface
supplied air;
snorkel. No
mixed gas or
saturation diving.
SCUBA or
surface supplied
air. Experimental
trawl fishery.
Oregon, USA All year
Permits issued
geographically until
2003, with half for the
southern coast and half
for the northern coast.
25% coast open under a
quota; 25% under
experimental fishery to
evaluate effects of
varying harvest levels;
50% of coast is no-take.
Dive gear and
trawl gear.
Recreational dive harvest
allowed below 6 m; Sea
cucumber trawl gear
prohibited in trawl
rockfish conservation
areas; small closed sites
around Channel Islands.
No area restrictions.
Trawl and dive
fishery.
British
Columbia,
Canada
October;
1-20
days
long
California
All year
Maine
OctJune; no
night
harvest
Newfoundland
Year
round
fishery
Canada
No area restrictions.
88
Dive fishery;
hookah and
SCUBA.
Trawl gear
(modified “urchin
drag”gear or
scallop drag
gear).
Harvested as
scallop bycatch,
also small dive
fishery (12
divers).
Quota for
each area;
quota for
recreational
harvest.
No quota.
THQ=385.6
mt;
individual
license
quotas of 4.5
mt; HAQ for
each area .
No quota.
No quota.
Max catch by
divers,
24,000 lbs
daily.
Table 4a. Specific details on temperate fisheries in North America
1.Alaska fishery is based on Parastichopus californicus Closed Season: selected to protect
spawning aggregations; can be closed early if harvest level is reached; Fishery management units:
each has biomass estimate completed within last two years; Quota: harvest level for each site based
on surplus production model that includes 1) an estimate of virgin population size and allowance of
harvest rate of 5%; and 2) additional conservative measures: quota is reduced to 50% of the harvest
rate derived from the model plus another 30% to account for field sampling variability (Ruccio and
Jackson, 2000).
2. Washington fishery is based on Parastichopus californicus and P. parvimensis Season: Year
round dive fishery; Experimental trawl fishery closed during soft-shell Dungeness crab periods and
in shrimp areas. Experimental trawl fishery in specific locations; beam trawl gear with max beam
width or otter trawl with minimum mesh size. Quota: for each area determined using surplus
production models and estimates of biomass from catch-effort data, video surveys, and dive
surveys. There is also a daily limit of 25 animals for two species (P. californicus and P.
parvimensis) for the recreational fishery (Bradbury, 1994)
3. Oregon’s fishery is primarily a dive fishery based on Parastichopus californicus; harvest by
trawl required an experimental gear permit until 2003. The target species has been placed under
category B of the Developmental Fisheries List, which include species with less potential for viable
fisheries; a permit is no longer required (McCrae, 1994; pers. comm).
4. British Columbia fishery is based on Parastichopus californicus Season: occurs during October
after reproduction (when internal organs are atrophied) to maximize product quality. Total quota is
determined from a precautionary fixed exploitation rate which is divided into harvest area quotas
based on an estimate of a coastwide density of 2.5 sea cucumbers per meter of shoreline, an
allowable harvest of 4.2% of biomass, shoreline length and average weight (Muse, 1998; Fisheries
and Oceans Canada, 2002).
5. California fishery started in 1978 and is based on Parastichopus californicus and P. parvimensis.
A special permit was required for sea cucumber harvest beginning in 1992-1993, with separate
permits for each gear type and a limit on the total number of permits implemented in 1997. There
are no restrictions on catch. Until 1996 an average of 75% of the annual catch was from the
southern California trawl fishery. Between 1997-199, the dive fishery accounted for 80% of the
take. Recent surveys show a 50-60% decline in abundance between 1994-1998, but no correlation
was noted between decline in abundance and data on landings. The only increase in abundance was
noted at two no-take reserves (39% increase) (Rogers-Bennett and One, 2001; Schroeter et al.,
2001).
6. Maine fishery is a low value/high volume fishery that started in 1994 and is based on Cucumaria
frondosa. The “urchin drag”gear used in the fishery is limited to 5”6” width and 22’ length; head
bail constructed of less than 1.5” round steel stock. Logbook data indicates fishing effort is
clumped with most cucumbers coming from three locations in eastern Maine (Feindel, 2002).
89
maturity requires a significant amount of data and the primary burden is placed on the fishermen, who must
determine the species being harvested and whether that species meets the minimumestablished size requirement.
Nevertheless, a number of countries such as Australia, Papua New Guinea, Fiji, and Tonga have recommended
or adopted separate size limits for each species (Table 7; Appendix I).
CONCLUSIONS
Commercially valuable sea cucumber populations are in decline or overexploited in many locations due to a
high demand for bêche-de-mer and other holothurian products, and the high value to fishermen, particularly in
developing countries where this provides a substantial component of their livelihood. One of the primary
reasons for the decline is that management measures have not been applied until after the stocks crashed. In
most countries, sea cucumbers have been harvested through open-access fisheries which initially target dense
populations with easy access, especially nearshore, shallow environments; stocks are initially underexploited,
but the catch keeps on growing and the industry flourishes. As the industry matures, the level of capture
becomes constant, but more fishing effort is needed to achieve these levels. As all of the suitable species and
size classes are removed from one area, the distribution of fishing effort expands to more remote areas and
deeper environments. While this practice may result in extensive areas that are essentially free of harvesting
pressure, it also leads to the localized depletion of stocks where fishing has occurred (Ibarra and Soberon,
2002).
Management strategies for holothurian fishery resources have many problems, and in most instances have been
reactive in response to dwindling stocks. Some of the issues hindering effective management include 1) a lack
of information on the population dynamics of exploited species and on holothurian biology and ecology; 2) few
reliable fishery and trade statistics; 3) illegal fishing and export; 4) unregulated or ineffective regulations combined
with insufficient enforcement; and 5) difficulties in measuring the effectiveness of management measures.
However, it is difficult to identify overarching problems with sea cucumber fisheries, as each fishery is unique.
Available information on the resource and the fishery varies by country or area, trade routes are complex and
existing fishery, and trade statistics are often insufficient to determine location of fisheries and catch on species
by species basis. In addition, monitoring is problematic, particularly in developing countries due to the widespread
and often remote nature of the fishery and lacking financial and human resources.
The management of sea cucumbers resources has to be approached on a site by site basis with appropriate
controls for each region. The most effective management plans are those that combine multiple controls, such
as a minimum size in combination with rotational fishing. In addition to effective fishery management plans and
regulations, additional capacity is necessary through training programs and better monitoring efforts for the
resource, the fisheries and exports, and enforcement programs must be in place. One way to achieve this is by
involving local communities, fishermen and other stakeholders in managing the resource and monitoring fishery
impacts. Several countries and regions are already exploring the possibility of developing bêche-de-mer
associations to control prices and maximize product quality. These associations are likely to be most effective
when they involve partnerships among the fishermen, processors, exporters and other resource users as well
as the resource management agencies, with increased involvement in all aspects of resource management and
monitoring. In addition, marine park rangers can be trained in dive survey methodology and holothurian
taxonomy, and can be encouraged to expand existing monitoring programs to include sea cucumbers. This will
provide a constant supply of field data on species presence, temporal and spatial distribution, and growth.
Marine parks and no-take reserves could also be sites for sea cucumber research.
90
Table 5. Examples of fishery management measures in the tropical western Pacific.
Location
and
species
Permits
Harvest area, species
and season
Australia:
Great
Barrier
Reef
Licensing
system and
logbooks.
Quota on
number of
licenses; 18
active
fishermen .
Permit system
through Island
Community
Councils.
Great Barrier Reef
Marine Park Act 1975
closed several reefs to
fishing. H. nobilis fishery
closed in October 1999.
None?
Hand or hand-held
non-mechanical
implements only; a
ban on SCUBA and
hookah gear; 7 m
maximum length of
Islander dinghies.
Total
allowable
catch of 260
mt and
minimum size
limits of 18
cm.
Australia:
Northern
Territory
6 commercial
licenses, 3 per
management
zone, 4 divers
per license
Hand collection
only by diving.
TAC is 380
mt (127 mt
white teatfish
and 253 mt of
other spp.;
minimum
sizes.
Fiji
Harvesting and
processing
restricted to
Fiji nationals .
PNG citizens
only; license
for storing or
export.
2 management zones;
collection restricted to
areas covered by water at
low tide; no take in
marine parks, reserves or
sanctuaries and around
particular islands and
shoals.
A 5.6 square mile area
around Namena Atoll
closed to harvest in 2001.
No export of H scabra.
Open season from 16 JanSep 30. Quota divided
into two value groups
(high and low). Torres
Strait fishery closed in
1992.
Scheduled closed season
and closed areas; 10 year
moratorium in 1999.
Use of SCUBA
gear prohibited, but
hookah was not
prohibited.
Hookah, SCUBA
and lights
prohibited.
7.6 cm 3 inch
minimum
export size.
Moratorium in certain
areas of Makira in 1994.
1998 ban on collection
and sale of sandfish.
Ban on SCUBA
and hookah in the
Western Province.
Australia:
Torres
Strait
Papua
New
Guinea
(PNG)
Tonga
Solomon
Islands
Exporters
limited to 10
licenses.
91
Gear type
Quota
Minimum
size: 15 cm;
TAC = 500 mt
(90% of the
estimated
yield .
Ban on SCUBA
and hookah.
TAC for each
province;
Minimum
sizes for 17
species (live
and dried) .
Min size for
some species
(live and
dried).
Table 6. Examples of controls and enforcement measures for sea cucumber fisheries in
temperate waters.
Location
British
Columbia
Canada
Alaska, USA
Washington,
USA
Oregon, USA
California,
USA
Maine, USA
Licensing
Limited entry;
85 licensed
fishers;
maximum 5
licenses per
vessel.
Divers
registered and
permitted.
Reporting
Fishers use
standard
logbooks .
Dive/harvest
logbook with
date, location
(GPS), depth,
bottom time,
quantity.
Limited entry;
Logbooks with
190 divers in
daily reporting
2000.
of catch to
avoid
exceeding
quota.
Fish receiving
Commercial
shellfish license tickets (dock
ticket) required
was required
for dive fishery from sea
cucumber
until 2003,
dealers with
when only 2
fishermen’s
permits were
name, location,
issued.
date and
amount.
Separate annual Dive and trawl
fisheries target
permits for
each gear type: different
species; all data
113 dive
permits and 36 lumped as sea
cucumber
sea cucumber
landings.
trawl permits.
16
Harvester
endorsements
Logbooks.
(only 3 active).
92
Validation
All landings are monitored by an
independent industry funded
firm; dockside landings only at
designated ports; license holders
pay a fee.
Divers can only obtain permits
for urchins or sea cucumbers but
not both.
Must submit logbooks every
month with data on date, depth
location and amount (number
and weight) collected.
Cucumbers are listed under
Developmental Fisheries species
list category B. As of 2004 a
permit is no longer required.
Limit permits by requiring a
minimum landing of 50 lbs
during the previous year. Trawl
fishery declined in 1998-1999
due to prosecution of 16 trawl
fishermen that fraudulently
obtained sea cucumber permits.
Limit licenses to fishermen that
landed >250,000 lbs in a
previous year. No incidental
take allowed, only take through
targeted, licensed fishery.
Table 7. Minimum size restrictions for tropical sea cucumbers. Other tropical nations
with minimum sizes for sea cucumbers include: 1) Queensland, Australia- 15 cm live
minimum size for all species; 2) Fiji- 7.6 cm size dried for all species; 3) Maldives- 15
cm size for H. atra only.
Scientific name
Trade name
Actinopyga lecanora
stone fish
Papua New Guinea
Live
Dry
15 cm
10 cm
H. scabra
H. scabra versicolor
sandfish
22 cm
10 cm
A. miliaris
black fish
15 cm
10 cm
A. mauritiana
surf red fish
20 cm
8 cm
H. fuscogilva
white teatfish
35 cm
10 cm
S. chloronotus
green fish
20 cm
10 cm
S. variegates (S.
hermanni)
curry fish
25 cm
10 cm
H. nobilis
black teatfish
22 cm
10 cm
26 cm
Thelenota ananas
prickly redfish
25 cm
15 cm
30 cm
Actinopyga lecanora
stone fish
15 cm
10 cm
T. anax
amberfish
20 cm
10 cm
B. argus
leopard (tiger) fish
20 cm
10 cm
Bohadschia vitiensis
brown sandfish
20 cm
10 cm
H. edulis
pink fish
25 cm
10 cm
Holothuria
fuscopunctata
elephant trunk fish
45 cm
15 cm
Halodeima
(Holothuria) atra
A. echinites
lolly fish
30 cm
15 cm
15 cm
25 cm
15 cm
12 cm
25 cm
7 cm
B. marmorata
mamorata (B.
similes)
brownfish
(deepwater red
fish)
93
W Australia
Live
16 cm
32 cm
Appendix I: Current Status of Existing Sea Cucumber Fisheries
Australia. Sea cucumber fisheries date back to the 1700s, with Indonesians most active participants of the
fishery until the late 1880s. Increasing interests in the 1980s led to an expansion of fisheries off Queensland,
Torres Strait and around the Great Barrier Reef (GBRMP), along with the development of management
measures and regulations. In the GBRMP intensive fishing in the mid 1980s-1990s led to depletion of the main
target species (H. nobilis) and the fishery on this species was closed in 1998 (Uthicke, 2003). Surveys in
GBRMP within fished areas and no-take areas showed that fishing reduced densities of sea cucumbers by
about 75%.
British Columbia, Canada: Sea cucumbers have been commercially harvested in British Columbia Canada
since 1971, with substantial changes in the management regime over time to address resource declines and to
avoid overfishing. The fishery was an open access fishery through 1990. Management measures include: 1) a
regional quotas and area closures first introduced in 1986; 2) a reduction in the regional quota in 1989 and
1991; 3) rotational harvest with six months of fishing followed by a two year closure in each defined site
between 1993-1996; 4) a license-type limited entry system was introduced in 1991 with individual quotas in
1995; and 5) adaptive management practices were introduced in 1997, with closed areas and areas open to
dive fishery, as well as an experimental fishery to assess affects of different harvest levels and determine what
is sustainable. In experimental areas resource managers conduct annual pre-harvest surveys, allow take at 0,
2, 4, 8 and 16% of the biomass, and then conduct follow-up surveys to evaluate effects of variable fishing
pressure on stocks. Three experimental fisheries are underway in three different habitat types, with annual
surveys and experimental fisheries continuing for at least 10 years. At the end of the study management
measures will be further refined.
Cook Islands: The only commercially exploitable sea cucumber species in Cook Islands is A. mauritiana,
with exports from 2 areas reported in the 1980s and some subsistence use in the southern islands.
Recommendations were presented in 1988 that included: 1) establishment of conservative management guidelines;
2) conducting baseline surveys prior to start of fishery; 3) implementation of seasonal closure during breeding
seasons; rotational fishing; quotas; minimum sizes; and reserve areas; 4) limited entry and required reporting
guidelines; and 5) a ban on the use of SCUBA (Adams, 1993b).
Cuba: A fishery was established in 1999, with over 3 million animals landed during the first two years by one
company operating out of 12 boats in the southeast region. The CPUE averaged around 1,153 +/- 630
animals per boat per day, with a decline throughout the year to about 350 animals/boat/day. In the southeastern
region, a quota of 611 tons has been established.
Ecuador: In 1989, sea cucumber fishermen from mainland Ecuador began setting up operations in the Galapagos,
as the fisheries off the coast of Ecuador were depleted. There was no management plan enacted at this time.
Populations of Stichopus fuscus became dramatically reduced almost immediately, prompting a ban on all
harvesting of sea cucumbers. Illegal fishing continued, however, and in early 1994, under protest by fisherman
and pressure from environmental groups the ban was lifted. In 1996 a consensus based participatory management
process was adopted for the sea cucumber fishery, with representatives of various stakeholders. In 1999
Ecuador passed the Galapagos Marine Management Plan and harvesting of sea cucumbers became regulated
under a concrete legal and conservation framework. Current management initiatives include a season of 60
consecutive days between March and May; open areas must have minimum observed density; zoning plan
with closed areas that correspond with spawning zones; minimum size (20 cm); and a fixed quota (Traffic
South America, 2000). In 2002 the Participatory Management Board (PMB) prepared a proposal for the five
94
year period fishing calendar. This proposal had the agreement from the local sectors (fishing, conservation,
tourism and Galapagos National Park) for the management of sea cucumber fisheries. This proposal was
approved by the Interinstitutional Management Authority (IMA) on February 25th and established that the
fishery would open when the results of a study on the sea cucumber population density was completed. The
study was carried out by the fishing sector, the Galapagos National Park and the Charles Darwin Foundation
from March 4th to April 10th, 2002 on 6 islands of the archipelago. The results from this joint study indicated
that none of the island in the study met the criteria of having a density of 40 sea cucumbers per 100 square
meters that were larger than 22 cm.
Egypt: A fishery began in 1998 with catch primarily associated with trawling. Expansion of fishery effort in
2000 led to a ban on sea cucumber fishing in 2001 until baseline stock assessments were completed. The
fishery was reopened in 2002, but population surveys indicated resource depletion and a new ban was declared
in 2003.
Fiji. Sea cucumbers are harvested for subsistence (sandfish) and export, with the export fishery dating back
to the early 1800s, when collection and processing facilities for sea cucumber were established in Fiji primarily
to supply Chinese markets (Adams, 1992). Numerous reports of overexploitation of sandfish are associated
with the bêche-de-mer boom of the mid 1980s, with exports increasing from less than 15 mt prior to 1982 to
717 mt in 1988. Severe depletion of stocks led to declining exports and a subsequent total ban on export of
sandfish; A. miliaris now accounts for up to 95% of the exports. Bêche-de mer Exploitation Guidelines were
first published by the Fisheries Division in 1985 with amended regulations in 1988 in response to a 10-20 fold
increase in exports (Adams, 1992).
India: Sea cucumbers are taken in a trawl fishery, as bycatch of “thallumadi”, a local fishing gear, and by skin
diving primarily in the Gulf of Mannar and Palk Bay. H. scabra, H. spinifera and B. marmorata were the most
important species over last 1000 years, but fishermen began collecting other species in 1990, in response to
high export value and population declines of the preferred species. In 1982, a ban on export of bêche-de-mer
below 3 inches was implemented and collection of all sea cucumbers was also banned in Andaman and
Nicobar Islands. A fishery exists in Gulf of Manner, Palk Bay, but CPUE and size of specimens has dramatically
declined in these areas. Problems with the fishery include an overlap between the peak fishing season and the
peak spawning season for H. scabra during July and October; other problems include habitat damage associated
with fishing gear. Drag-nets used for sea cucumbers in shallow sea grass beds cause severe destruction of sea
grasses. In 2001, all sea cucumbers added to Schedule I list of the Wildlife Protection Act, which bans their
collection. However, illegal fishing continues and most stocks are depleted (Nithyanandan, 2003).
Indonesia: Indonesia has the worlds largest sea cucumber fishery with estimated exports increasing from 878
mt in 1981 to over 4600 mt per year from 1987-1990 (Tuwo and Conand, 1992). There are few management
measures, although regulations exist in various regions on trawling for sea cucumbers and maximum densities
for cage culture of juveniles collected from the wild. Some locations are implementing various voluntary community
based conservation measures.
Japan: Sea cucumbers have been consumed locally for centuries, with one species (S. japonicus) harvested in
local waters and now also under intense aquaculture. The catch of S. japonicus in Japan declined from 25,000
mt in 1983 to 7000 mt in 1995. Hatchery production increased substantially during this period (Ito and Kitamura,
1998). Japan prohibits fishing between March and November to take into account spawning and seasonal high
water temperatures. In addition, area closures are in place in some locations and gear restrictions have been
implemented (Arakawa, 1990).
95
Kenya: Sea cucumbers are collected for export with little or no local consumption. Exports have increased
since 1993.Exports increased from 78-86 mt per year between 1989-1991, to 277 mt in 1992, followed by
a sharp decline in the next 3 years (14, 41, 55 mt respectively). Fourteen species are exported (Marshall et al.,
2001). The only regulations in place are licenses, which are required to collect or trade in sea cucumbers,
although most fishermen do not hold licenses.
Madagascar: Export fishery began in 1921, with exports of 50-140 mt annually. Exports increased from 56
mt in 1986 to over 500t in 1991 and 1994. Although it is now illegal to fish with SCUBA, this has been difficult
to enforce. Shared management was introduced in 1998, which included a partnership between the Madagascar
National Trepang traders group and the government resource managers to administer management and
exploitation of trepang (Conand et al., 1998). Madagascar fishers and exporters also formed the National
Association of Sea Cucumber Producers (ONET). Some of the proposed initiatives of these associations
include: studies of current status of resource; formulation of a monitoring and joint management system using
simple assessment methods to evaluate resource and its fluctuation; creation a management manual; and sea
farming experiments.
Malaysia. There are three different fisheries for sea cucumbers, including one near Pulua Langkawi with well
established trade routes through Thailand; a small artisanal fishery in western Malaysia with a single fisherman,
and an expanding fishery along the coast of Sabah in northeast Borneo. In Pulua Langkawi, one target species,
S. hermanni, has been depleted and may possibly be extirpated around Langkawi Islands. In Sabah, annual
catch was about 400-500 mt, while annual catch in the 1990s has fallen to around 100 mt. Currently there are
no countrywide regulations of the sea cucumber fishery (Baine and Sze, 1999).
Maldives. Bêche-de-mer production began around 1986, with three species targeted: T. ananas, H. nobilis
and B.marmorata. Exports increased from 3 mt in 1986 to 740 mt in 1990 (Reichenbach et al., 1998). The
only formal regulations are a ban on SCUBA implemented in 1996. The Bay of Bengal programme made
recommendations that include a 4-5 yr ban on take of Thelenota ananas, a min size of 6 inches for H. atra,
and they discourage night fishing.
Mexico: In Baja California, harvesting of the sea cucumber Isostichopus fuscus for export to Asian markets
rose very sharply between 1985 and the mid nineties. A permitted commercial dive fishery was established in
1992. In 1994 a closed season was imposed in Baja and size limits for Isostichopus fuscus and P. parvimensis
were established; in May of 1994 I. fuscus was declared in danger of extinction by the National Institute of
Ecology of Mexico (NOM-059-ECOL-94) with a ban on fishing (Castro, 1995). Illegal fishing continued into
1997, when I. fuscus stocks reached 2% of their original estimated size. In March 200, I. fuscus was placed on
a “species under special protection” list, which authorizes scientific research by fishermen and government
scientists. Illegal fishing continues (Ibarra and Soberon, 2002).
Micronesia: A small fishery for A. mauritiana and H. whitmaei occurred in Saipan, CNMI during 1996
and 1997, but was halted in early 1997 due to declining CPUE (Trianni, 2003). The Saltonstall Kennedy grant
program funded a five year project in Micronesia (American Samoa, Guam, and FSM) on resource surveys,
aquaculture and management with emphasis on three species. The project resulted in a general moratorium on
export harvests in Palau and portions of the FSM and the development of a generic sea cucumber Management
Plan for Micronesian states (Richmond, 1996).
96
Mozambique. The sea cucumber fishery targets 11 species, with apreference for H. scabra, H. nobilis, H.
fuscogilva, H. atra, A. echinites and A. mauritiana. Collection occurs in intertidal areas while wading (by
women and children) and in deeper areas with snorkel and SCUBA gear (men); some bycatch in trawl and gillnet fisheries is reported. Between 1979-1990 exports fluctuated from about 20-110 mt; during the 1990s
exports fluctauated between 17.7-52.4 mt with a drop to 2.9 mt inm 1997 (Marshall et al., 2001). with a high
fluctuation in exports. The primary management measure has involved closed seasons, although fishermen
continue to exploit the resource during closed periods. The fishery has been closed in one area due to
overexploitation.
New Caledonia. The bêche-de-mer fishery dates to the 19th century, with a recent revival in 1983 and harvest
of 55-180 mt per year until 1990, when the fishery declined. About 100 fishermen were involved in the fishery
in 1993 at the tribal level or in cooperatives on the northeast Coast of Caledonia (Conand and Byrne, 1993).
There is no formal management by the government, but local communities have implemented certain conservation
measures. In 1992 the people of Arama undertook a voluntary suspension of fishing by during the crab season
(April and January). Fishers of Nepoui Poum and Pouebo also established independent minimum size limits.
Panama. Exploitation of sea cucumbers began in an unplanned way, with a permit granted by the government
in 1997 for harvesting and processing bêche-de-mar in Bo-cas del Toro. The negative effect of this unmanaged
extraction occurred immediately and the permit was revoked 30 days later. An estimated 750 000 sea cucumbers
of the three species had been caught during the period, and illegal fishing continues. A recent study comparing
population survey data with fishing effort reported severe overfishing and suggested these species will collapse
within a year if fishing pressure is maintained or permitted (Guzman and Guevera, 2002). The authors recommend
no fishing of A. multifidus and I. badionotus in the entire archipelago for 3-5 years followed by a tightly
controlled harvest for Bo-cas del Toro that includes the creation of no-take areas that are stocked with adult
holothurians. They also recommended a fishery for H. mexicana with limited access, quotas, season, minimum
size and site-based closures in depleted areas that are currently affected by illegal fishing (Guzman and Guevera,
2002).
Palau, Ponphei and Samoa: A number of species are harvested in the Pacific Islands for subsistence use,
with some species harvested for their body wall while others are harvested for their gonads and intestines
(Lambeth, 2000). Traditional knowledge and resource management practices are commonplace, including
collection only during morning hours over four mornings twice per month (Palau), use of a finger to induce
evisceration instead of cutting the animal thereby leading to faster regeneration times (Pohnpei), and a requirement
that removal of the intestine must be processed on the spot, with animals returned to the water (Samoa).
Philippines. The sea cucumber fishery is a year round activity with a peak season from March to June.
Holothurians are collected primarily by women during low tide at night by walking along the intertidal zone,
while men snorkel or use hookah gear to collect from deeper areas. Exports of sea cucumbers from the
Philippines have occurred for over 300 years, with little or no local consumption (Jun, 2002). Export statistics
available since 1970 indicate that the Philippines has emerged as the second largest producer in the world, with
catches of around 20,000 mt per year since the mid 1980s (Conand and Byrne, 1993). Exports have been
maintained at about 1000 mt, although there has been a decline in high value species compensated for with low
value species. There is very little information on the fishery, and there are no management measures specific for
sea cucumber fisheries. Many areas stripped of high commercial value species and others of all species
(Trinidad-Roa, 1987).
97
Papua New Guinea (PNG). The fishery dates back to the 18th century, with some local consumption of H.
scabra. After a period of low activity from 1977-1985, the fishery has been an important source of income for
coastal communities (Conand and Byrne, 1993). The primary target in 1989 was H. scabra, leading to
establishment of a minimum size in 1996 as a measure to protect stocks. In Torres Strait, problems of illegal
fishing in Australian waters led to a closure of the fishery in 1993, which was extended through 1995 (Lokani,
1996). A closed season, licensing and logbook system proposed but not adopted (Lokani et al., 1996). In
2001, a National Bêche-de-mer Fishery Management Plan was adopted. The Plan outlines access, size and
catch limits, and storage and export requirements and includes a closed season (Oct 1- Jan 15), total allowable
catch by Province and species, and a licensing and logbook system (Polon, 2003). The Plan also encourages
provinces in forming Provincial Management and Advisory Committees. The Provincial Fisheries Management
Committee made thorough stock assessment in Oct/Nov 2001 throughout Milne Bay and found that most
commercial sea cucumber species occur at very low densities. Fisheries data indicate that catch of high value
species declined from 36% in early 1990s to 15% in 2002. Although regulations are in place for sea cucumber
fisheries, illegal fishing occurs during closed seasons; quotas are often exceeded; and prohibited gear (hookah
and lights) is still used (D’Silva, 2001).
Seychelles. A small open access fishery has occurred since the 1950s, with recent increases in harvest of six
species mainly for export markets. In 1999 management measures were introduced by the Seychelles Fishing
Authority, including The Seychelles Fishing Authority requires licenses for fishing and processingsea cucumber
fishermen to be licensed,, with 25 fishing licenses granted per year (Seychelles Nation Online, 2003).Thailand.
Sea cucumbers are harvested for local consumption and export with H. scabra and H. atra being most
popular. An export fishery emerged in the late 1970s, with collection primarily by hand during low tide. As
resources declined, snorkelling to depths of 5-10 m became popular; use of SCUBA or hookah is not reported. Overexploitation and a shift to less valuable species have been reported. There is currently an
absence of management, with recommendations for the establishment of minimum sizes and stock management
in marine national parks and sanctuaries (Bussarawit and Thongtham, 1999).
Solomon Islands. The fishery increased from 8 mt in 1985 to 622 mt in 1992, which represented 62% of the
countries exports worth $3.4 million USD (Richards et al., 1994). Since 1992, landings have decreased to
240 mt in 2001, with over 75% of the landings derived from species with medium and low commercial value.
The South Pacific Commission Inshore Fisheries Research Project 1992 recommended community management,
alternate closed seasons of 6-12 months, possible application of size, effort, gear or seasonal limitations that
apply to subsistence and commercial fishing, establishment of marine reserves, and monitoring of catch data.
None of these recommendations were adopted except for a ban on the use of SCUBA (Adams, 1993). Due
to failure of centralized management of the fishery, there is a push to return to customary marine tenure with
active participation by fishers and resource owners in implementing management measures (Ramofafia et al.,
2003) .
98
Tanzania. Sea cucumbers are collected by hand-picking, free diving and SCUBA, with a small amount of
bycatch associated with commercial trawlers. Collection is year round, with peak periods between March and
May and September to November. The fishery targets 7 species, with a lower take of 13 other species. The
fishery is currently unregulated (Mmbaga and Mgaya, 2003). Landings increased from 324 mt in 1989 to
1460 mt in 1995, although official exports during the 1990s ranged from 189-565 mt with a peak in 1994 and
subsequent declines to about 277-324 mt in subsequent years (Marshall et al., 2001). Separate licenses are
required for traders and exporters and exports are taxed.
Tonga. The fishery began in the early 1980s with rapid expansion in the late 1980s and early 1990s with the
introduction of assisted underwater breathing apparatus. By 1994, exports exceeded 60 mt. In 1996 a
widespread public awareness campaign targeted towards fishermen was initiated to develop the fishery in a
more sustainable manner. The government encouraged community management, recommending bêche-demer liason officers, closed seasons at the end of each year, and closed areas (Ministry of Fisheries 1996). In
1999, a ban with a ten year moratorium on all species was implemented.
Tuvalu. A small fishery existed between 1979 and 1982. The fishery was revived in 1993, with 871 kg of
exports; exports increased four-fold in 1994-1995 (Belhajali, 1997). The fishery is not regulated, but there are
recommendations to ban use of SCUBA and hookah gear to harvest sessile organisms including sea cucumbers.
United States. Sea cucumber fisheries in the U.S. are primarily temperate water fisheries with commercial
harvest by trawl or dive gear occurring off the east coast (Maine) and west coast (California, Oregon, Washington and Alaska). There is currently little to no harvest in tropical regions. On a state-wide basis, these
appear to be sustainably managed, although localized depletions have been reported.
Vanuatu. No fishery in Vanuatu has operated under a formal management plan. The Fisheries (Amendment)
Act No. 2 (1989) provides the Minister and the Director with broad discretionary power to manage the
country’s fish stocks. An annual quota of 40 mt was established by Ministerial order in 1991 and put in place
in 1996. Cooperative management was introduced between 1990-1993, in which the government fisheries
department provides scientific information and advice, while coastal villages assume the bulk of the responsibility
for local management. While bêche-de-mer fishing per se was not being managed, many villages employ total
fishing ground closures which constitute de facto bans on bêche-de-mer harvesting.
Venezuela. One year licenses for 200kg/wk were first issued in 1993 and later suspended; four licenses were
issued in 1994 for the original site plus a new area (Rodríguez and Marques-Pauls, 1998).
99
Literature Cited
Adams, T. 1992. Resource aspects of the Fiji beche-de-mer industry. Beche-De-Mer Information Bulletin,
SPC 4: 13.
Adams, T. 1993. Management of beche-de-mer (sea cucumber) fisheries. Beche-De-Mer Information Bulletin,
SPC 5: 15-22.
Adams, T. 1993b. Resource profile No. 6, Bêche-de-mer, rori of the Cook Islands, 1988.
Arakawa, K.Y. 1990. A handbook on the Japanese Sea cucumber- its biology, propagation and utilisation.
Beche-De-Mer Information Bulletin, SPC 4: 5-8.
Baine, M. and C.P. Sze, 1999. Sea cucumber fisheries and trade in Malaysia. 49-63. In Baine M (ed). The
Conservation of sea cucumbers in Malaysia: their taxonomy, ecology and trade. Heriot-Watt University,
Edinburgh. ISBN 0-9531575-3-9. pp.49-63.
Baine M. and P.S. Choo. 1999. Sea cucumber fisheries in Malaysia, towards a conservation strategy. BecheDe-Mer Information Bulletin, SPC 12:6-10.
Battaglene, S. 1999. Culture of tropical sea cucumbers for the purpose of stock restoration and enhancement.
The Conservation of sea cucumbers in Malaysia: their taxonomy, ecology and trade. Heriot-Watt University,
Edinburgh. ISBN 0-9531575-3-9. pp. 11-25.
Battaglene, S. 2000. ICLARM restocks sandfish at Western Province. Beche-De-Mer Information Bulletin,
SPC 13: 30-31.
Battaglene, S.C. and J.D. Bell, 1999. Potential of the tropical Indo-Pacific sea cucumber, Holothuria scabra,
for stock enhancement. In: E.S. Moksness et al., eds. Proceedings of the First International Symposium
on Stock Enhancement and Sea Ranching. Blackwell Science. 478-490.
Belhajali, K. 1997. Beche-de-mer production in Tuvalu. Beche-De-Mer Information Bulletin, SPC 9: 2-4.
Beumer, J. 1992 Queensland’s bêche-de-mer fishery. Beche-De-Mer Information Bulletin, SPC 4: 12.
Bradbury, A. 1994. Sea cucumber dive fishery in Washington State. Beche-De-Mer Information Bulletin,
SPC 6: 15-16.
Buitrago, J and J.A. Boada, 1996. La pesca de la holothuria Isostichopus badionotus en el oriente de Venezuela.
Memoria Sociedad de Ciencias Naturalas La Salle. 146:33-40.
Bussarawit S. and N. Thongtham. 1999. Sea cucumber fisheries and trade in Thailand. Pp.26-36. In Baine
M (ed). The Conservation of sea cucumbers in Malaysia: Their taxonomy, ecology and trade. HeriotWatt University, Edinburgh. ISBN 0-9531575-3-9.
Castro, L.R.S. 1995. Management options of the commercial dive fisheries for sea cucumbers in Baja California,
Mexico. Beche-De-Mer Information Bulletin, SPC 7:20.
Chen, J. 2003. Overview of sea cucumber farming and sea ranching practices in China. Beche-De-Mer
Information Bulletin, SPC 18: 18-23.
Conand, C. 1986. The fisheries resources of the Pacific Islands. Part two. Holothurians. FAO Fish Tech. Pap,
272.2: 108 pp.
Conand, 1993. Reproductive biology of the holothurians from the major communities of the New Caledonia
Lagoon. Mar. Biol. 116:439-450.
Conand C. and Byrne, M. 1993. A review of recent developments in the world sea cucumber fisheries. Marine
Fisheries Review. 55:1-13.
Conand, C. 1997. Are holothurian fisheries for export sustainable? Proc. Eighth Intern. Coral Reef Symp.
Panama. 2: 2021-2026.
Conand, C. 1999. World sea cucumber exploitation and the market for trepang: an overview. In Baine M (ed).
The Conservation of sea cucumbers in Malaysia: Their taxonomy, ecology and trade. Heriot-Watt University,
Edinburgh. ISBN 0-9531575-3-9 pp1-10.
100
Conand, C. 2001. Overview of sea cucumbers fisheries over the last decade- What possibilities for durable
management? Echinoderms 2000: 339-344.
Conand, C and M. Byrne. 1993. A review of recent developments in the world of sea cucumber fisheries.
Mar. Fisheries Rev. 55: 1-13.
Conand, C, M.De San, G. Refeno, G. Razafintseheno, E. Mara and S. Andriajatovo. 1998. Sustainable
management of the sea cucumber fishery sector in Madagascar. Beche-De-Mer Information Bulletin,
SPC10:7-9.
D’Silva, D. 2001. The Torres Strait bêche-de-mer (sea cucumber) fishery. Beche-De-Mer Information Bulletin,
SPC 15: 2-4.
Dance, S. I. Lane, and J. Bell. 2000. Variation in short-term survival of cultured sandfish (Holothuria scabra)
released in mangrove-seagrass and coral reef flat habitats in Solomon Islands.
Dalzell P., T.J.H. Adams, and N.V.C. Polunin. 1996. Coastal fisheries in the Pacific Islands. Ocean and
Marine Biology: an Annual Review. 34:395-531.
Feindel, S. 2002. Status of the Maine Sea Cucumber (Cucumaria frondosa) Fishery. Submitted to Standing
Legislative Committee on Marine Resources. Department of Marine Resources, Maine. 35 pp.
Fisheries and Oceans Canada, 2002. Pacific region integrated management plan. Sea cucumber by dive
October 1, 2001 to September 30, 2002. 16 pp.
Fuente-Betancourt, de la G.M., A. Jesús-Navarrete, E. Sosa-Cordero, and M.D. Herrero-Perezrul. 2001.
Assessment of the sea cucumber (Echinodermata: Holothuroidea) as potential fishery resource in Banco
Chinchorro, Quintana Roo, Mexico. Bull. Mar. Sci. 68: 59-67.
Guzman, H.M. and C.A. Guevara. 2002. Population structure, distribution and abundance of three commercial
species of sea cucumber (Echinodermata) in Panama. Carib Jour Sci. 38:230-238.
Holland, A. 1994. The beche-de-mer industry in the Solomon Islands: recent trends and suggestions for
management. Beche-De-Mer Information Bulletin, SPC 6:2-9.
Ibarra, A.A. and G.R. Soberon. 2002. Economic reasons, ecological actions and social consequences in the
Mexican sea cucumber fishery. Beche-De-Mer Information Bulletin, SPC 17:33-36.
Infofish trade news, 2002
Ito, S. 1995. Studies on the technological development of the mass production for sea cucumber juvenile
Stichopus japonicus. Saga Prefectural Sea farming Center, Japan. 87 pp. Beche-De-Mer Information
Bulletin, SPC 10: 24-28.
Ito, S and H Kitamura. 1998. Technical development in seed production of the Japanese sea cucumber,
Stichopus japonicus. Beche-De-Mer Information Bulletin, SPC 10:24-28.
James, D.B. 2003. Captive breeding of the sea cucumber Holothuria scabra from India. Abstract: Workshop
on Advances in sea cucumber aquaculture and management. FAO. Oct 14-18 2003.
Jangoux, M., R. Rasolofonirana, D. Vaitilingon, J-M. Ouin, G. Seghers, E. Mara, and C. Conand. 2001. A
sea cucumber hatchery and mariculture project in Tulear, Madagascar. Beche-De-Mer Information Bulletin,
SPC 14:2-5.
Jiaxin, C. 2003. Present status and prospects of sea cucumber industry in China. Abstract: Workshop on
Advances in sea cucumber aquaculture and management. FAO. Oct 14-18 2003.
Jun, A. 2002 Trepang exploitation in the Philippines: Updated information. Beche-De-Mer Information Bulletin,
SPC 17: 17-21.
Kinch, J. 2002. Overview of the beche-de-mer fishery of Milne Bay Province, Papua New Guinea. BecheDe-Mer Information Bulletin, SPC 17: 2-16.
Lambeth, L. 2000. The subsistence use of Stichopus variegates (now S. hermanni) in the Pacific Islands.
Beche-De-Mer Information Bulletin, SPC 13: 18-21.
Lokani, P. 1996. Illegal fishing for sea-cucumber (beche-de-mer) by Papua New Guinea artisanal fishermen in
the Torres Strait protected zone. Beche-De-Mer Information Bulletin, SPC 8:2-6.
101
Lokani, P, P. Polon and R. Lari. 1996. Management of beche-de-mer fisheries in the Western province of
Papua New Guinea. Beche-De-Mer Information Bulletin, SPC 8:7-13.
Marshall, N., S.A.H. Milledge and P.S. Afonso. 2001. Trade Review. Stormy Seas for Marine Invertebrates.
Trade in sea cucumbers, seashells and lobsters in Kenya, Tanzania and Mozambique. TRAFFIC East/
Southern Africa. 70 pp.
McCrae, J. 1994. Oregon developmental species. Sea cucumbers Parastichopus sp. Oregon Dept. of Fish
and Wildlife. 1-4.
McElroy, 1990.Beche-de-mer species of commercial value-an update. Beche-De-Mer Information Bulletin,
SPC 2:2-6.
Mercier, A., R. Ycaza Hidalgo, and J-F Hamel. 2003 Aquaculture of the Galapagos sea cucumber Isostichopus
fuscus. Abstract: Workshop on Advances in sea cucumber aquaculture and management. FAO. Oct. 1418 2003.
Ministry of Fisheries. 1996. Status and management of inshore fisheries in the kingdom of Tonga: beche-demer. Beche De-Mer Information Bulletin 8:12-1321.
Mmbaga, T.K. and Y.D. Mgaya. Studies on sea cucumber in Tanzania and the gaps towards resource inventory
and management . Abstract: Workshop on Advances in sea cucumber aquaculture and management.
FAO. Oct. 14-18 2003.
Moore, A. 1998. Preliminary notes o the exploitation of holothurians in the new Wakatobi Marine National
Park, Sulawesi, Indonesia. Beche De-Mer Information Bulletin 12: 15-16.
Morgan, A. 2000. Induction of spawning in the sea cucumber Holothuria scabra (Echinodermata:Holothuridae).
Journal of the World Aquaculture Society. 31 (2):186-194.
Munro, J.L. and J.D. Bell, 1997. Enhancement of marine fisheries resources. Reviews in Fisheries Sciences.
5:185-222.
Muse, B. 1998. Management of the British Columbia Sea Cucumber Fishery. CFEC 98-4N Alaska Commission
Fisheries Entry Commission. 25 pages.
Nithyanandan, 2003. Sea cucumbers. A resource in peril. Indiscriminate fishing of sea cucumbers in Indian
Seas has led to their overexploitation. Samudra November: 24-26.
Pitt, R. 2001. Review of sandfish breeding and rearing methods. Beche-De-Mer Information Bulletin, SPC
14: 14-21.
Polon, P. 2003. The Papua New Guinea National Beche-de-mer fishery management plan. Abstract: Workshop
on Advances in sea cucumber aquaculture and management. FAO. Oct. 14-18 2003.
Preston, G. 1990. Beche-de-mer survey in Tonga. Beche-De-Mer Information Bulletin, SPC 2:2-6.
Preston, G.L. 1993. Beche-de-mer. In: Wright A, Hill L. (eds). Nearshore resources of the South Pacific.
Institute of Pacific Studies, Suva, pp.371-408.
Preston, G.L. and Lokani P. 1990. Report of a survey of the sea cucumber resources of Ha’apai Tonga. June
1990. South Pacific Commission. Noumea New Caledonia.
Purcell, S., D. Gardner and J. Bell. 2003. Developing optimal strategies for restocking sandfish: a collaborative
project in New Caledonia. Beche-De-Mer Information Bulletin, SPC 16:2-4.
Ramofafia, C. M. Gervis and J. Bell. 1995. Spawning and early larval rearing of Holothuria atra. Beche-DeMer Information Bulletin, SPC 7:2-6.
Ramofafia C., I. Lane and C. Oengpepa. 2003. Customary marine tenure in Solomon Islands: a shifting
paradigm for management of sea cucumbers in artisanal fisheries. Abstract: Workshop on Advances in
sea cucumber aquaculture and management. FAO. Oct. 14-18 2003.Reichenbach N, Y. Nishar and A.
Shakeel. 1998. Laamu atoll mariculture project: Low profile cage for retaining sea cucumbers. BecheDe-Mer Information Bulletin, SPC 10:14.
Richards, A.H., L.J. Bell, and J.D. Bell. 1994. Inshore fisheries resources of Solomon Islands. Mar. Pollut.
Bull. 29: 90-98.
102
Richmond, R.H. 1996. Suggestions for the management of sea cucumber resources in Micronesia. Results of
the workshop “A Regional Management Plan for A Sustainable Sea Cucumber Fishery for Micronesia.
Technical Report 101. University of Guam Marine Laboratory. 68 pp.
Rodríguez, E., and S. Marques Pauls. 1998. Sea cucumbers fisheries in Venezuela. Proc. 9th Inter. Echinoderm
Conf. 513-516.
Rogers-Bennett, L. and D.S. One, 2001. Sea cucumbers. California Department of Fish and Game California’s
Living Marine resources: A status report. 131-134.
Ruccio, M.P. and D.R. Jackson, 2000. Red sea cucumber and green sea urchin commercial fisheries management
plans for the westward region, 2000-01. Regional Information Report No. 4K00-59. Alaska Department
of Fish and Game Division of Commercial Fisheries.
Samyn, Y. 2000. Conservation of aspidochirotid holothurians in the littoral waters of Kenya. ). Beche-De-Mer
Information Bulletin, SPC 13: 12-17.
Schroeter, S.C., D. Reed, D. Kusher, J. Estes and D.S. Ono. 2001.The use of marine reserves in evaluating
the dive fishery for the warty sea cucumber, Parastichopus parvimensis. Can. J. Fish Aquat Sci. 58:17731781.
Seychelles Nation Online, 2003. Protection for sea cucumbers. www.seychelles-online.com.sc/archives/
102501103.html 2 pp.
Trianni, M.S. 2002. Summary of data collected from the sea cucumber fishery on Rota, Commonwealth of the
Northern Mariana Islands. Beche-De-Mer Information Bulletin, SPC 16:5-11.
Trianni, M. S. 2003. Evaluation of the resource following the sea cucumber fishery of Saipan, Northern Mariana
Islands. Proc. 9th Intl Coral reef Symp. 2:829-834.
TRAFFIC South America. 2000. Evaluation of the trade of sea cucumber Isostichopus fuscus (Echinodermata:
Holothuroidea) in the Galapagos during 1999. Quito. 19 pp.
Trinidad-Roa, M.J. 1987. Beche-de-mer fishery in the Philippines. Naga, the ICLARM quarterly, Manila,
10(4): 15-17.
Tuwo, A. and C. Conand. 1992. Developments in beche-de-mer production in Indonesia during the last
decade. Beche-De-Mer Information Bulletin, SPC 4:2-3.
Tuwo, A. 2003. Status of sea cucumber fisheries and farming in Indonesia. Abstract: Workshop on Advances
in sea cucumber aquaculture and management. FAO. 14-18 2003.
Uthicke S. and J.A.H. Benzie. 1999. Allozyme variation as a tool for the beche-de-mer fisheries management:
A study on Holothuria scabra (sandfish). Beche-De-Mer Information Bulletin, SPC 12: 18-23
Uthicke S. and J.A.H. Benzie. 2000. Effect of bêche-de-mer fishing on densities and size structure of Holothuria
nobilis (Echinodermata: Holothuridae) populations on the Great Barrier Reef. Coral reefs. 19: 271-276.
Uthicke S. and J.A.H. Benzie. 2001. Restricted gene flow between Holothuria scabra (Echinodermata:
Holothuroidea) populations along the north-east coast of Australia and the Solomon Islands. Mar. Ecol.
Prog. Ser. 216:109-117.
Uthicke, S. 2003 Over fishing of holothurians: lessons from the Great Barrier Reef. Abstract: Workshop on
Advances in sea cucumber aquaculture and management. FAO. Oct. 14-18 2003.
Yaqing, C., Y Changqing and S. Xing. 2003 Sea cucumber (Apostichopus japonicus) pond polyculutre in
Dalian, Liaoning Province, China. Abstract: Workshop on Advances in sea cucumber aquaculture and
management. FAO. October 14-18 2003.
Yin-Geng, W., Z Chun-yun, R Xiao-Jun, C. Jie-Jun, S. Cheng-Yin, S. Hui-ling and Y. Jing-Ping. 2003 Diseases
of cultured sea cucumber (Apostichopus japonicus) in China. Abstract: Workshop on Advances in sea
cucumber aquaculture and management. FAO. October 14-18 2003.
103
CITES and Sea Cucumbers
Glenn Sant
TRAFFIC Oceania, Australia
This paper gives an overview of and highlights issues of relevance to this workshop on the following topics:
1. General background on the Convention on International Trade in Endangered Species of Wild Fauna and
Flora (CITES), the Appendices and differences between Appendices II and III;
2. The inclusion in Appendix III of Isostichopus fuscus by Ecuador;
3. The differences between implementing the provisions of the Convention for species of sea cucumber listed
in Appendix II and III; and
4. Non-CITES related institutional measures.
This document expresses the views of TRAFFIC and should not be assumed to reflect the views of the CITES
Secretariat. The content of this background paper has been derived from a number of sources, but of particular
relevance are Sant (1995), Willock (2002) and Willock et al. (in prep.).
Background to CITES and Sea Cucumbers
At its 12th meeting (Santiago, 2002), the Conference of the Parties adopted Decisions 12.60 and 12.61
related to sea cucumbers within the families Holothuridae and Stichopodidae. The CITES Secretariat was
mandated through Decision 12.61 to convene a technical workshop on the conservation of sea cucumbers in
co-operation with relevant bodies. The outcomes are to be reviewed by the Animals Committee. The CITES
Secretariat consulted the Animals Committee in August 2003 concerning the workshop’s proposed objectives,
agenda, participation and practical arrangements (see document AC19 Doc. 17, and the relevant report from
the AC Working Group). The objectives of the workshop were agreed as follows:
a) to review information on the status, catches and bycatches of and trade in specimens of sea cucumbers
within the families Holothuridae and Stichopodidae; and on domestic measures for their conservation,
including considerations of the adequacy of these measures;
b) to establish conservation priorities and actions to secure the conservation status of sea cucumbers within
the families Holothuridae and Stichopodidae, addressing inter alia trade monitoring and controls, national
legislation and regulations, fisheries management options, conservation management and research,
enforcement and capacity building; and
c) to formulate findings and recommendations that can contribute towards the discussion paper on the biological
and trade status of sea cucumbers within the families Holothuridae and Stichopodidae to be prepared by
the Animals Committee.
Of particular relevance is the entry into force in October 2003 of the inclusion by Ecuador of Isostichopus
fuscus in Appendix III.
104
General background to CITES
CITES has three Appendices that list species of wildlife. Each Appendix has different requirements and levels
of protection afforded to the species listed in them through the Convention text and Resolutions and Decisions
agreed by the Parties to the Convention. A proposal by a Party for a species to be included in Appendix I or
Appendix II is discussed and put to a vote at the regular meetings of the Conference of the Parties. Listing
proposals may be co-sponsored by other Parties. The criteria to be used for determining whether species
should be included in Appendix I or II are contained in Resolution Conf. 9.24 (Rev.
CoP12) on Criteria for amendment of Appendices I and II. In case the proposal concerns a species that
occurs in more than one country, proponent Parties have normally to consult with other range States about its
proposal. Decisions on amending Appendix I and II require the support from at least two-thirds of Parties
present at the meeting of the Conference of the Parties and voting, including decisions to list or de-list a
species, or to transfer it between the Appendices. Any Party may enter a reservation on an Appendix I or II
listing within 90 days after the adoption by the Conference of the Parties, which results in the Party being
treated as a non-Party to the Convention with respect to that species, until the reservation is withdrawn. A
Party may unilaterally decide to list a species in Appendix III at any time. A reservation on an Appendix III
listing can be taken by a Party at any time and in relation to either the species or certain parts or derivatives
thereof.
By including an animal species in Appendix I or II, live and dead specimens, and all readily recognizable parts
and derivatives thereof become subject to the provisions of the Convention. The inclusion can concern an
entire species, subspecies or geographically separated populations.
The role of each of the three CITES Appendices
Appendix I
An Appendix-I listing offers the highest protection for a species under CITES and includes species that are
threatened with extinction and potentially at risk from international trade. Trade in wild-collected specimens of
these species must be subject to particularly strict regulation and only authorized in exceptional circumstances
(Wijnstekers, 2001). There are nearly 600 animal species and 300 plant species included within Appendix-I.
Appendix II
An Appendix II listing of a species does not necessarily mean that it is currently threatened with extinction nor
that trade in that species will be limited, however any such trade must be determined not to be detrimental to
the survival of the species in the wild, and should only involve specimens that were obtained in compliance with
national laws for the protection of fauna and flora. This means that trade in Appendix-II species should only
involve wildlife that was legally acquired and sustainably produced. Appendix II includes species that may
become threatened if their trade is not effectively regulated. Through the adoption of listing criteria, the CITES
Parties have concluded that Appendix II should include species for which the harvesting of specimens from the
wild for international trade has, or may have, a detrimental impact on the species by either exceeding, over an
extended period, the level of harvesting that can be continued in perpetuity, or reducing the species to a
population level at which its survival would be threatened by other influences.
105
To ensure that trade in an Appendix II-listed species is non-detrimental, a number of steps must be completed
prior to export. First, the Scientific Authority of the State must advise that the export would not be detrimental
to the survival of the species. Second, the Management Authority of the State must be satisfied that the
specimens were not illegally obtained. The Scientific Authority may also determine that limits should be placed
on the export of a species in order to maintain it throughout its range at a level consistent with its role in the
ecosystems in which it occurs. Annual quotas are one example of such limits. The Management Authority is
ultimately responsible for the issuing of permits.
In relation to importation of Appendix II-listed species, the importing State must require the prior presentation
of the export permit or re-export certificate. Some importing states, most notably the members of the European
Union, have taken stricter measures and require the prior issuance of an import permit before Appendix-II
specimens can be imported. If a species is re-exported, the re-exporting State’s Management Authority must
be satisfied that the species was imported in accordance with CITES provisions.
The above requirements relate to species that are harvested from areas that are under the jurisdiction of a
State. Provisions also exist under CITES for “introduction from the sea” (Art. I (e)) which is defined as
“…transportation into a State of specimens of any species which were taken in the marine environment not
under the jurisdiction of any State”. To date CITES has not formally clarified what constitutes waters under a
State’s jurisdiction beyond the 12 nautical mile territorial sea.
Appendix III
Appendix III is unique among the three CITES Appendices in that a Party may unilaterally list, and de-list, a
species at any time. However, the Parties have developed a recommended process to be followed by Parties
wishing to list a species in Appendix III. While still able to submit a species for listing at any time, Resolution
Conf. 9.25 on Inclusion of species in Appendix III requests Parties to first consult more widely with any other
range States and the Animals Committee before moving to include a species in Appendix III. A listing Party is
also requested to ensure that its “…national regulations are adequate to prevent or restrict exploitation and to
control trade, for the conservation of the species” and that its “…national enforcement measures are adequate
to implement these regulations” (Res. Conf. 9.25).
Despite Appendix III being an integral part of CITES a number of Parties do not have domestic legislation in
place enabling them to enforce the listing of a species in that Appendix (Anon., 2003a).
The main purpose of Appendix III is to provide assistance to a Party in the enforcement of its national regulations
for a species subject to exploitation for international trade. In practice this circumstance usually arises when
there is a significant level of illegal trade that the Party needs the co-operation of other Parties to address. The
listing in Appendix III therefore provides for this co-operation through enabling CITES Parties to apply their
domestic laws to ensure that trade in the listed species occurs in a manner consistent with the laws of the State
of origin for that species (Anon., 2003b; Willock et al., in prep.).
Any country having listed a species in Appendix III must issue an export permit prior to the specimens being
exported. An export permit is granted when the Management Authority of the State is satisfied that the specimen
was not illegally obtained. Unlike with species listed in Appendix II, Parties issuing export permits for Appendix
III specimens are not required to ensure that exports are within sustainable levels, i.e. to make a “non-detriment”
finding. Exports from Parties that are range States for the species that have not listed it in Appendix III must be
accompanied by a Certificate of Origin. Resolution Conf. 12.3 on Permits and Certificates recommends that
106
Certificates of Origin follow the format for other CITES permit documents and be issued by the Management
Authority. These certificates can be valid for a period of up to 12 months (other documents are generally valid
for only six months). Parties re-exporting specimens of the species must issue a Certificate of Re-export,
which, as with Certificates of Origin, should be issued by the Management Authority and follow the format for
other CITES permit documents.
Parties importing specimens of species listed in Appendix III must confirm that the shipments are accompanied
by a Certificate of Origin from a Party that has not listed the species or an export permit where the exporting
Party has listed the species. In the case of re-export, a Certificate of Origin from the re-exporting State stating
that the specimen was processed in that State or is being re-exported is required upon import. On the basis of
this certificate, the importing State decides if the provisions of the Convention have been met. A State may
query the validity of a certificate.
Key differences between Appendix II and III
In contrast to Appendix II there are no provisions relating to introduction from the sea under Appendix III. In
addition, as noted above, unlike the granting of export permits in relation to species listed in Appendix I and
Appendix II, there is no requirement for exporting Parties that list the species in Appendix II to make a nondetriment finding for Appendix III species. Further, Management Authorities issuing Certificates of Origin do
not have to ‘be satisfied’ that specimens to be exported have been obtained in accordance with their national
conservation laws, a requirement for exports of Appendix II species.
A further difference is that the provisions of Appendix III only apply to the parts or derivatives specified in the
listing. For example, the listing of Big-leaf Mahogany Swietenia macrophylla in Appendix III included an
annotation designating that only logs, sawn wood and veneer sheets were included under that listing. By
contrast, an Appendix II listing for animal species applies to the species as a whole, and no parts or derivatives
can be exempted. For plants in Appendix II, however, only whole specimens (live or dead) are covered, with
other parts and derivatives only included if specified in accompanying annotations.
Another difference with important implications for marine species is in relation to what are commonly referred
to as look-alike species. Article II 2(b) of the Convention allows for species to be included in Appendix II if
this is necessary to ensure the effective regulation of trade in species listed in that Appendix owing to trade
threats. Resolution Conf. 9.24 requires that this should occur when “…the specimens resemble specimens of
a species included in Appendix II under the provisions of Article II, paragraph 2(a), or in Appendix I, such that
a non-expert, with reasonable effort, is unlikely to be able to distinguish between them.” This is an important
provision for marine species as these are often traded in high volumes and in a highly processed state, making
some species difficult to distinguish from others. There is no such provision under CITES relating to the listing
of look-alike species in Appendix III (Willock et al., in prep.).
A final difference is that in all circumstances personal and household effects are exempt under Appendix III.
This means that international movement of products derived from marine species that are considered to be
personal or household effects, for example necklaces made from shark tooth, require no CITES documentation.
107
Table 1: Summary of main differences between Appendix II and Appendix III Source:
Adapted from Anon. (2003b) and Willock et al.( in prep.)
Provision
Appendix II
Appendix III
Listing process
Proposal requires 2/3 majority A Party may unilaterally list
support
to
be
accepted; a species at any time
proposals are generally to be
decided upon at meetings of the
Conference of the Parties
Introduction from the Sea
Provisions apply
No provision
Non-detriment finding
Required
Not required
Nature of listing
By species;
By
species
but
may
annotated to include only
species of fauna cannot be
certain parts or derivatives
annotated to exempt certain parts
of a species of fauna or flora
and
derivatives
from
the
provisions of the convention
parts and derivatives (other than
whole specimens) must be
specifically
included
by
“annotation” for species of flora
Reservation
Only within 90 days of the Can be taken at any time
listing
Can be taken in respect to
Only in respect to the species as any particular part or
a whole
derivative
Look-alike species
Look-alike species may also be No provision for the listing
listed
of look-alike species
Personal and household Included
under
effects
circumstances
108
certain All personal and household
effects are exempt
Issues surrounding the listing in Appendix III of Isostichopus fuscus by Ecuador1
The listing in Appendix III of Isostichopus fuscus by Ecuador provides useful background to examining issues
associated with management of sea cucumber fisheries, trade in specimens and the implementation of a CITES
listing.
Background
The sea cucumber I. fuscus is distributed in the Eastern Pacific from Baja California, Mexico to Ecuador,
including the Revillagigedo, Cocos and Galapagos Islands (Hickman, 1998). I. fuscus has an elongated body,
with a soft texture and thick borders. It is dark brown in colour and spotted with orange papillae. It can grow
up to 39 cm in length and is sexually mature at around 21 cm, corresponding to 4 to 5 years of age (HerreroPerezrul et al., 1999). In the Galapagos the species is distributed throughout the archipelago usually in shallow
waters (to 39 m depth; but mainly between 5 to 12 m) (Altamirano and Martinez, 2002), therefore it is easily
harvested with the use of a hookah2. Since 1999 the sea cucumber fishery has been the most important source
of income of the Galapagos fishing sector (Murillo et al., 2003). The domestic market for sea cucumber in the
Galapagos and Ecuador mainland is extremely small and the vast majority of the harvest is exported; for
example around 90% of the harvest was exported in 2002. In the Galapagos, the sea cucumber fishery is
authorised exclusively by the Inter-Institutional Management Authority (AIM).3
Mexico, the only other country that has significantly traded this species, declared it as "threatened" in 1994 and
closed the fishery. Since March 2000, the species has been included under a special protection regulation and
commercial fishing permits have not been issued for Holothurians since that time.
Despite a range of management measures being in force for the sea cucumber fishery in Ecuador I. fuscus has
remained the subject of over-harvest and extensive illegal trade from the Galapagos to supply international
markets. On 16 October 2003 the Ecuadorian government included I. fuscus in CITES Appendix III as a
complementary control measure to address international trade of this species.
Commercial fishery
I. fuscus is the only species of sea cucumber commercially harvested in Ecuador’s waters. Harvesting
commenced in the mainland waters of Ecuador in the late 1980’s and within a short time there was a steep
increase in the national harvest, from 3 t in 1988 to 29 t in 1991. The resource became over-exploited in
mainland waters and the harvest subsequently moved to the Galapagos in 1991 (De Paco et al., 1993).
In 1994 the sea cucumber fishery was opened for three months with a maximum quota of 500,000 sea
cucumbers. However, around 6 million sea cucumbers were harvested during the first half of the season, which
led to the early closure of the fishery. A ban on harvest was subsequently introduced until 1998.
In 1999 AIM authorised the opening of the fishery on an ‘experimental’ basis, with a decision to be made on
whether or not to allow it to continue based on the outcomes from the 1999 season. Since then, a fishery has
been authorised every year with that decision based on results from monitoring the sea cucumber populations
as well as socio-economic factors.
In addition to the wild capture fishery for I. fuscus, attempts to farm the species have recently commenced in
abandoned shrimp ponds on mainland Ecuador. By the end of 2003 there had only been success in production
109
up to the larval stage therefore no trade has taken place. Sea cucumber farming has taken place in several
Asian countries (China, Indonesia, India, Philippines and Viet Nam) for restocking and commercial culture as
measures to reduce pressure on wild populations. There are two main growing methods for sea cucumbers:
monoculture of holothurians in old shrimp ponds, or policulture with shrimp. Both proved to be financially
profitable (Chang et al., 2003). It is not known whether farming of I. fuscus has commenced in any other
country (Hamel et al., 2003).
Table 2: Captures of sea cucumbers in the Galapagos Source: Altamirano and Martínez
(2002); M. Altamirano, Charles Darwin Research Station, in litt. to A. Sancho,
TRAFFIC South America, November 2003; M.V. Toral-Granda in litt. to A. Sancho,
TRAFFIC South America, January 2004
Year
Quota authorised
(units)
Number of sea
cucumbers
captured (units)
Total green
weight (t)
Average green
weight of sea
cucumbers
harvested
1999
4,000,000
4,401,657
1,512 0.344
2000
4,500,000
4,946,947
1,561 0.316
2001
4,000,000
2,672,345
924 0.346
2002
No quota
established
8,301,449
1,660 0.200
2003
4,700,000
5,005,574
1,200 0.240
Table 2 shows a decline in the average weight per sea cucumber harvested from 1999 to 2003, with a total
decrease of 33% over the five-year period. This is shown most starkly in 2002 when, despite a three-fold
increase in the number of sea cucumbers harvested compared to the previous year, the total biomass of the
harvest only increased by just over half. The decrease in the weight of sea cucumbers harvested is highlighted
by the fact that in the 2003 56% of the harvest was below the 20 cm minimum size limit (Murillo et al., 2003).
Management measures for the Galapagos fishery
There is a comprehensive management regime in place for the sea cucumber fishery in Ecuador covering both
the harvesting of the resource and subsequent movement of the product within the country. Management
measures in place include the following:
-
Minimum size for both dried (6cm) and green (20cm) sea cucumbers
No-take areas
Closed seasons
Limits on the number of licences granted to harvest sea cucumbers
Annual quota (expressed in numbers of sea cucumbers)
Chain of custody from harvest to export
Scientific monitoring of the population
Carriage of government observers if requested
110
A significant amount of further work is also currently underway in the Galapagos to improve the existing
conservation and management measures within the Galapagos Marine Reserve. Improvements in such areas
as monitoring, control and surveillance of commercial fishing vessels are anticipated within the next couple of
years, including the implementation of satellite-based vessel monitoring systems.
Trade in I. fuscus from Ecuador
From 1990 to 2003, Ecuador exported 554 t of dried sea cucumbers, with an FOB value of almost USD 7.5
million FOB price. Table 3, below, shows recorded exports of dried sea cucumber from Ecuador since 1990
and the FOB price.
Table 3: Ecuadorian exports of dried sea cucumbers in tonnes
and FOB value Source: Banco Central del Ecuador, 2003.
a
until September 2003
Year
Weight (t)
FOB (USD)*
1990
2.93
1991
8.12
1992
32.06
121,034
1993
2.01
16,000
1994
23.12
2,493,398
1995
40.20
417,100
1996
7.67
38,361
1999
112.64
885,261
2000
110.37
1,212,744
2001
48.48
457,710
2002
116.51
1,072,711
2003
50.01 a
1,170,698
Total
554.12
7,473,078
1997
1998
111
Although the sea cucumber fishery was closed during 1993, 1995, 1996, 1997 and 1998 exports of sea
cucumbers were recorded in most of those years. A possible explanation for this is that export of dried products
can occur at any time. Therefore, products legally acquired in previous years may be exported in a later year
due to the long shelf life of the dried product. An alternative explanation is that these exports represent illegally
harvested sea cucumber. It is not possible to determine which explanation is correct, or whether the answer lies
in a combination of the two.
Comparison of export data with official import data from Taiwan (province of China) and Hong Kong reveals
significant discrepancies. From 1998 to 2002, imports of dried sea cucumbers from Ecuador into Hong Kong
and Taiwan (province of China) in each year exceeded the reported exports by at least ten per cent and in
some years by 25 per cent. In addition to imports of dried sea cucumber, Taiwan (province of China) Customs
data also record a total of 211 t of frozen sea cucumbers and 100 t of salted or in brine product as having been
imported from Ecuador over that period. On the basis of import figures from Hong Kong and Taiwan (province
of China) alone, the Ecuadorian export data would appear to substantially under-record exports of sea
cucumbers.
Illegal trade
There have been numerous cases of illegal harvest and trade of sea cucumbers detected by authorities in the
Galapagos. These include harvest outside the fishing season, harvest in no-take areas and harvest under the
allowed minimum size.
The illegal harvest is taken out of the Galapagos by diverse means, including hidden in ships, probably in larger
foreign vessels that illegally enter the Galapagos Marine Reserve (GMR) to pick up illegal cargo of shark fins
on their way to non-Ecuadorian ports and in luggage declared to contain personal effects (M. Altamirano,
Charles Darwin Research Station, pers. comm. to A. Sancho, TRAFFIC South America, October 2003).
One of the known routes for the laundering of illegal Galapagos sea cucumbers includes final processing in
Guayaquil, on the Ecuador mainland, followed by overland transportation to Peruvian ports where it is exported
as a local product. The volume of domestic sea cucumber trade in Peru is much larger than in Ecuador, not only
because several species are harvested but also because there is a higher local consumption due to a significant
population of Asian origin (J. Vizcaíno, Galapagos National Park Service, pers. comm. to A. Sancho, TRAFFIC
South America, October 2003).
Within the Galapagos and the Ecuador mainland, a regulated chain of custody has been established for sea
cucumbers. However it has not prevented the continuation of illegal harvest for international trade. This is in
part due to the fact that the control ends when the product is exported therefore illegally harvested sea cucumbers
that circumvent domestic controls may then freely enter international trade.
CITES Appendix III listing of I. fuscus
The listing of I. fuscus in CITES Appendix III entered into force on 16 October 2003. As of 1 February 2004,
no CITES Party had entered a reservation to this listing. This is an important consideration given that a reservation
by a major importing country would result in the listing not being implemented by that Party. The regulated
chain of custody ceases when the cargo leaves Ecuador and little is known of what happens to it from this point
on to the end consumers in international markets. The Appendix-III listing is potentially a useful complementary
measure to the current chain of custody requirements as it will require documentation to accompany the sea
cucumbers wherever the cargo goes.
112
Implementation issues relating to the I. fuscus listing in Appendix III
Look-alike species
One of the main issues to be addressed for the successful implementation of the listing is that of look-alike
species to I. fuscus, as many sea cucumber species are very similar when dried or frozen. When processed,
most of their external characteristics disappear and only the presence or absence of spikes, which remain after
processing, can be used by a non-expert to separate them in these two large groups, each of which include
many different species. It is worth noting that Taiwan (province of China) has separate import codes for spiked
and non-spiked sea cucumbers (S. Lee, TRAFFIC East Asia, in litt. to A. Sancho, TRAFFIC South America,
January 2004). More recent research has found that body wall ossicles, unique taxonomic characters to each
species of sea cucumber, remain intact after all processing techniques in I. fuscus, thus providing a potential
tool to be used for identification (Verónica Toral, in litt. to A. Sancho, TRAFFIC South America, February
2004).
Some 76 countries and territories are known to have traded sea cucumber species with Hong Kong in the past
10 years (S. Lee, TRAFFIC East Asia, in litt. to A. Sancho, TRAFFIC South America, January 2004).
Development of an identification guide that allows clear identification of I. fuscus from all other sea cucumbers
subject to international trade is essential. Given the influential role of major consumers in Asia such as China
(including Hong Kong and Taiwan) in the international trade of sea cucumber, it is essential to ensure adequate
provisions in these countries to implement the Appendix III listing of I. fuscus.
In the absence of the ability to identify I. fuscus from other sea cucumber species in trade, it is likely that
illegally harvested specimens will not be detected and so will be traded as part of a general group of sea
cucumbers of similar appearance. The listing not only includes whole specimens, but all derivatives. This poses
extra difficulties with identification.
Range States for I. fuscus
All range States for the species are Parties to CITES4, however Ecuador is the only country that has included
I. fuscus in Appendix III thus far. Nevertheless, other potential exporting range States must issue CITES
certificates of origin for their exports of this species.
The effectiveness of the implementation of Appendix III in helping close down illegal trade routes would
increase significantly if all range States were to list I. fuscus in Appendix III. This would then mean that all I.
fuscus in international trade would be accompanied by export permits determining the legality of the specimens
in trade. The absence of the requirement under a Certificate of Origin to make a finding that the specimens have
been legally obtained provides for the continuing possibility that products illegally harvested and transshipped
to another range State from the Galapagos may enter international trade.
Ecuador’s decision to include I. fuscus in Appendix III is being viewed as a pilot exercise and other countries
are awaiting the results before making any further decisions (S. Lasso, CITES Management Authority, Ministry of Environment of Ecuador, pers. comm. to A. Sancho, TRAFFIC South America, November 2003). Of
relevance to the decision of other range States may be the fact that Guzmán et al. (2002) state that management and conservation problems in Ecuador has led to traders searching for alternative sources of the product
in the region. This has already resulted in the development of unregulated or illegal fisheries for sea cucumbers
along the Pacific and Caribbean coasts of countries in tropical America, mainly Venezuela and Mexico.
113
Trade in specimens from captive breeding5
Although there is no trade yet in captive bred I. fuscus from Ecuador it is likely to occur in the future. It is worth
noting that if the Management Authority is satisfied that the specimens were bred in captivity in compliance with
the provisions of the Convention and Resolution Conf. 10.16 (Rev.) on specimens of animal species bred in
captivity, a certificate of captive breeding may be issued by the Management Authority in lieu of an export
permit. Captive breeding as defined by CITES is distinct and dealt with differently from the situation where
specimens are taken from the wild (often as an egg or juvenile) and reared in captivity. This is referred to as
“ranching”.
Conclusions drawn from an examination of the Appendix III listing of I. fuscus
The Ecuadorian Government has utilized the possibility within CITES to unilaterally include a species in Appendix
III with the expectation that the co-operation of other Parties will assist in addressing the illegal harvest of I.
fuscus for international trade. With the listing only recently entering into force it is unclear the extent to which it
will assist in addressing current issues relating to the fishery. However it is likely that, even with effective
implementation of the Appendix-III listing, there will remain a need to strengthen national controls and management
measures.
A significant amount of work is currently underway in the Galapagos to improve the existing conservation and
management measures for the Galapagos Marine Reserve. Improvements in such areas as monitoring, control
and surveillance of commercial fishing vessels are anticipated within the next couple of years, including the
implementation of satellite-based vessel monitoring systems. Effective implementation of the CITES Appendix
III listing of I. fuscus would therefore complement efforts being undertaken at a local and national level.
There are a number of areas in which further action may need to be taken in order to ensure the effective
implementation of the Appendix III listing of I. fuscus including:
• Develop and distribute an identification guide for I. fuscus with descriptions of the exported products to
enable identification of the species by the authorities of exporting, re-exporting and importing countries.
• Provide training in Appendix-III implementation to management and control authorities, including I. fuscus
identification and familiarization with CITES export permits. Such training should be undertaken on a
regular basis as rotation of control personnel (airports, ports) is high.
• Improve the awareness and understanding of CITES within the fisheries sector in the country by giving
short training seminars on CITES including the role of the Appendices and its implementation.
• Maintain a high level of communication with other range States to create awareness of the I. fuscus listing
and assist in identifying potential illegal imports from Ecuador.
• Urge range States to reconcile harvest of I. fuscus within their waters with the export figures to help
prevent illegally obtained products from Ecuador being exported from that country.
• The Central Bank of Ecuador should assign species- and product-specific export codes for sea cucumbers
in order to improve ability to trace exports of this commodity.
114
Comparison between Appendix II and III listings of sea cucumber species
Look-alike provisions of the Convention and the recording of species in trade
The Ecuador example above identified the issue of look-alike species as being crucial to the success of the
Appendix III listing given the difficulty in identifying individual species of sea cucumber when traded in dried or
frozen form beyond generic ‘spiked’ and ‘non-spiked’ categories. This issue will arise regardless of whether a
sea cucumber species is listed in Appendix II or Appendix III. Given that illegal trade is often a factor in Parties
listing or proposing the listing of a species, the possibility of a listed species being traded under a different
name, and thus avoiding CITES requirements, is a serious one.
Identification guides are a widely used tool under CITES to assist in differentiating traded specimens at the
species level. Such guides have been developed for a range of listed marine species such as corals while a
seahorse identification guide is currently in preparation. Further, increasingly sophisticated identification tools
are being developed to identify species in trade, including the use of genetic testing and microscopic examination.
In the case of sea cucumbers there has not been extensive work to date on readily available means to identify
individual species in trade (Bruckner et al., 2003) with the Ecuador listing likely to be the first test of the
potential to develop such tools.
As noted, there are unique taxonomic characters to each species of sea cucumber that remain intact after
processing. However, as this technique requires the use of fixing agents over a number of hours and the use of
microscopic analysis, it is probably an analysis that only an expert would use. This raises the important issue of
the appropriateness of different identification techniques, particularly where species are traded in large volumes
(for example, in 2003 there were over five million sea cucumbers harvested in Ecuador alone). In some cases,
more complex techniques may be most efficiently used to confirm species identification where there is already
some suspicion that illegal trade is occurring. In addition, sophisticated tools such as DNA testing or examination
of microscopic details may also prove beyond the current capacity of a number of developing countries, from
whose waters much of the trade in sea cucumbers originates.
In relation to Appendix II in addition to the potential use of identification tools CITES provides that other
species may also be listed in Appendix II in order to ensure effective control over trade in the species of
conservation concern. This provision would enable, for example, all species of ‘spiked’ sea cucumbers in trade
to be listed in Appendix II were one such species of sea cucumber listed.
Species listed in Appendix II as look-alike species are subject to the same provisions as those listed due to
concerns over their conservation status. Therefore, this approach would not remove the requirement for the
exporting Party to ensure that the trade was without detriment to the species. However, experience under
CITES with listings of species groupings or orders, such as Antipatharia spp. (black corals) and Scleractinia
spp. (stony corals), has shown that this can result in low reliability of trade data for individual species within the
listing due to permitting and reporting at taxonomic levels higher than species6. In some instances this has led to
a reduced confidence that trade is not negatively impacting on a particular species’ conservation status. For
example if all species in the family Stichopodidae or the genus Stichopus were listed, trade data on individual
sea cucumber species might still remain elusive if correct permitting and reporting did not occur. In relation to
Appendix III, there is no provision under CITES for look-alike species to also be listed in that Appendix.
Therefore, unless a Party took the step of unilaterally listing all potential look-alike species, identification
problems at species level would require different approaches to be taken cantered on the availability of
identification guides and information-sharing about trade routes of legal and illegal product.
115
Availability of trade data
Regardless of in which Appendix a species is listed, it is important that correct marking of shipments and
identification of species is made to not only enable compliance with CITES permitting, but also to ensure that
accurate recording is taking place in import and export statistics.
Trade information at the importing level provides export countries with valuable information on what is being
exported from their shores. In many cases this may be the only current information available to the exporting
country to interpret what level of harvesting of their resources is occurring. Given the importance of this
information for the collection of data and for use in relation to helping monitor the implementation of a CITES
listing, the need for adequate Customs codes for the reporting of export and import must be one of the highest
priorities for action in relation to sea cucumber conservation. This involves the need for countries to have
adequate codes to include all commodity types that are being traded. Consideration needs to be given to
determining at what minimum taxonomic level trade information should be collected. At a minimum the major
importing countries of China, Hong Kong, Singapore and Taiwan (province of China) need to have adequate
Customs codes in place as this would then cover the majority of the world’s sea cucumber trade. These issues
should be addressed regardless of any future listings of sea cucumber species in CITES.
Non-detriment findings
Export of a sea cucumber species listed in Appendix II requires the prior grant by the Party of an export
permit. This requires the Scientific Authority of that Party to advise the Management Authority of that Party that
the export will not be detrimental to the survival of that species. Appendix III listings do not require the issuing
of non-detriment findings prior to granting an export permit or a certificate of origin. This raises the question of
the potential basis for non-detriment findings by exporting Parties.
There are currently few countries that actively manage their fisheries for sea cucumbers (Bruckner et.al, 2003;
Sant, 1995) with notable exceptions such as Ecuador, the United States of America, Australia, Canada and
New Zealand (Anon., in prep.; Bruckner et al., 2003; Willock et. al., in prep.). Further, there is a lack of
availability of information on many biological characteristics of sea cucumber species and harvest levels (Bruckner
et al., 2003). The lack of active management and information in many range countries on which to base a nondetriment finding for sea cucumber species may be a significant short to medium term impediment to an effective
listing in Appendix II. There is a need to collect biological and catch/trade information on sea cucumbers,
particularly in the major exporting countries, so that sufficient knowledge can be gained to determine how a
non-detriment finding can be made for particular populations of sea cucumber.
Management regimes for fisheries vary in complexity from stock assessment models reliant on extensive catch
and monitoring data to the application of relatively simple measures such as closed areas and minimum sizes.
Depending on the nature of the resource an effective management regime may not necessarily require the most
extensive and complex measures to be applied to support a non-detriment finding. There is, however, a fine
balance between allowing harvest at levels that are probably sustainable and being precautionary enough to
ensure the survival of the species is not put at risk.
116
There is no “one fit all” method within CITES that is applied to non-detriment findings and hence it is the
responsibility of a Party to decide at which level a harvest is sustainable and how that decision is reached. An
important function within CITES exists whereby through the Animals and Plants Committees, species that are
being traded at significant levels at what may potentially be of detriment to the species may be subject to review
Hence there are provisions within CITES to identify and prevent long-term trade at levels that are not sustainable.
Legality findings
The lack of active management in most range States for sea cucumber species raises a second question in
relation to implementation of any future Appendix II listings – the basis for a finding that specimens being
exported were legally obtained.
An absence of management measures may make this a relatively straightforward finding in theory, there potentially
being no domestic laws that could be contravened. However, a finding by a Management Authority that a
specimen had been legally obtained under such circumstances may be incongruous with any attendant nondetriment finding required for an export permit to be granted. In certain circumstances it may be considered
that unregulated harvest was not a potential threat to the conservation of the species concerned however in
most cases where harvest is stimulated by a demand for trade this is unlikely to be the case. Findings on the
legality of the acquisition of specimens for trade may also be complicated by difficulties in identifying individual
species if subject to different management regimes. For any future Appendix-II listing two key elements would
therefore need to be addressed by exporting countries: first, to implement domestic management regulations
for sea cucumbers in support of sustainable harvest of the resource and, second, to ensure the ability exists to
determine when these regulations were contravened.
In relation to Appendix III, only the second of these two key elements arises. This is because a listing in
Appendix III requires (under Resolution Conf. 9.25) the listing Party to already have in place national regulations
relating to the management of the species in question. Range States not having listed the sea cucumber in
Appendix III are only required to issue a Certificate of Origin, which does not require a finding that the
specimens were legally obtained. With regard to the current listing of I. fuscus in Appendix III if any other
range State wished to also list the species in that Appendix they would first need to ensure that adequate
domestic measures were in place for the species.
Captive Breeding
Captive breeding of sea cucumber species occurs in a range of countries. In some cases the purpose of these
operations is the re-seeding of depleted stocks while in other cases it is rearing for the purposes of commercial
trade. Consideration needs to be given to the potential conservation impacts of captive breeding and what
methods may need to be developed to distinguish individuals sourced from captive breeding facilities and wildcaught individuals.
Whether a sea cucumber is listed on CITES or not there are two particular areas of relevance for the conservation
of sea cucumber species. The first is the issue of management at the national level and whether the captive
breeding has any impact on the status of the wild population; for example, whether wild harvested parental
stock is utilized and whether there is any re-seeding of wild stocks. The second issue is whether captive-bred
individuals entering trade should be considered separate from wild harvested individuals for the purposes
of, for example, monitoring of quotas.
117
If wild and captive-bred specimens are to be treated in a different manner this then raises the question of the
ability to recognize certain specimens as captive bred, which may require the development of tagging or
marking procedures.Under CITES there are specific provisions relating to the treatment of captive bred animals,
with the Management Authority needing to be satisfied that specimens have been captive bred. In such
circumstances a certificate of captive breeding may be granted in lieu of export permits or other certificates.
Costs and benefits of listing of Sea cucumbers in Appendix II and III
In terms of conservation costs and benefits of listing sea cucumber species in either Appendix II or III of
CITES, it is clear that a number of implementation issues would need to be addressed in order for benefit to be
derived from such a listing.
Identification of individual species in trade is perhaps of most importance as conservation benefit will be
dependent on the ability to ensure that harvest of a species of concern is occurring at a sustainable level. The
potential for illegally harvested species of sea cucumber to be traded as non-listed species would also need to
be addressed, particularly in relation to Appendix III listings where illegal trade is often the main threat to the
conservation of species.
It is possible that a listing in Appendix II or Appendix III of CITES would stimulate management action being
taken in range States for sea cucumber species that would improve the conservation status of these species, a
situation that may not occur in many countries in the absence of a listing. This could involve management being
put in place and/or non-detriment findings being undertaken to ensure that the harvest of sea cucumbers is
sustainable. The other main benefit derived from a CITES listing is the checks that occur through the CITES
processes such as the significant trade review, mentioned earlier.
The costs, which are primarily financial in nature, are that all the implementation issues such as species identification,
issuing of permits, non-detriment findings etc. require a certain level of administrative investment and sufficient
investment in science.
Confiscation and disposal of confiscated specimens
Under Article VIII 1(b) Parties are required to implement domestic legislation allowing them to confiscate
illegally traded specimens so as to ensure enforcement of the provisions of the Convention.
In relation to trade in sea cucumbers under CITES Appendix II, any dead (e.g., dried, salted or in brine)
specimens seized by the Management Authority of a Party may be subsequently sold by that Authority. Resolution
Conf. 9.10 (Rev) provides that such confiscated specimens ‘…be disposed of in the best manner possible to
benefit enforcement and administration of the Convention’. No such guidance is given with respect to AppendixIII specimens, with the exception that specimens not be re-exported if there is evidence they were imported in
violation of the Convention. Depending on the legislation of individual Parties, the proceeds from the sale of
confiscated sea cucumbers could be used to recover costs incurred in the seizure and sale or more generally be
attributed to enforcement of CITES by that Party. Subsequent export or re-export of confiscated sea cucumbers
would then require a special notation to be made on the export permit that these were confiscated items. The
majority of international trade in sea cucumber species is in dead animals, however it is possible that live
specimens of species destined for the aquarium trade would be confiscated if CITES provisions were not met.
In such cases Parties have identified a decision-making process to determine the best means of disposal of live
animals including the possibility of returning the animal to the country of origin, destroying it or maintaining it in
captivity.
118
CITES provisions for Introduction from the Sea
Introduction from the sea is an important provision under the Convention for many off-shore marine species
that are harvested from high seas areas. However, while some species of sea cucumbers may occur in high
seas areas, harvest occurs from waters under the jurisdiction of a State. It is unlikely that provisions relating to
introduction from the sea will be relevant to sea cucumbers under CITES.
Non-CITES related institutional measures
Improved domestic management of sea cucumber fisheries is clearly a precursor to any future complementary
use of the provisions under CITES. The identification of minimum requirements for data collection and monitoring
of sea cucumbers and their associated fisheries to ensure their conservation is required in support of the
development of management measures. Such information is fundamental for the management of fisheries to
ensure these stay within sustainable levels, whether or not there are any future listings in CITES.
In Ecuador and in some other fisheries around the world a number of different management tools have been put
in place to limit effort within fisheries, assist with the collection of particular fishery dependent catch/trade
information and directly protect species at particular biological developmental stages.
Within Article 63 of the United Nations Convention on the Law of the Sea (UNCLOS) Coastal States which
are fishing shared stocks from within their EEZ’s should either directly through bilateral or multilateral arrangements
manage their stocks or through action within sub-regional, regional or international agreements. There are
numerous Regional Fisheries Bodies which include all marine resources under their preview, but they vary as to
the extent to which they either offer management advice on fisheries or directly manage fisheries. For example
the South Pacific Community (SPC) advises its members on scientific and management measures for marine
species, but do not directly manage fisheries resources.
Recently the members of the Food and Agriculture Organization (FAO) have agreed on International Plans of
Action, one of which being the conservation and management of sharks. Such a plan could possibly be considered
by FAO members for sea cucumbers. FAO also provides expert management, marketing and trade advice on
many marine species.
Institutions such as these offer opportunity to coordinate management of shared stocks and/or improve national
management of sea cucumber fisheries.
For Discussion
This paper discusses the requirements and implications in relation to a listing of sea cucumbers in either
Appendices II or III of CITES. This discussion has identified particular issues that would need to be addressed
for such listings to be effectively implemented. Regardless of any future listings of sea cucumbers in the CITES
Appendices discussion is also required concerning improved management of sea cucumber fisheries and trade
at the national and international level.
119
References
Altamirano, M. and Martínez P. (2002). Propuesta para inclusión del pepino de mar, Isostichopus fuscus
en el apéndice III de CITES. Galápagos, Ecuador. Unpublished report.
Anon. (2003a). Appendix III and national legislation. CITES World 11:14.
Anon. (2003b). What is Appendix III and how does it work? CITES World 11:2.
Anon. (in prep.). Fisheries Snaphots On Trade and Conservation Issues: Sea Cucumber. TRAFFIC North
America, Washington D.C., USA.
Bruckner A, Johnson K. and Field J. (2003). Conservation strategies for sea cucumbers: Can a CITES
Appendix II listing promote sustainable international trade? SPC Beche de mer Information Bulletin
18.
Chang Yaqing, Yu Changqing and Song Xin. (2003). Sea cucumber (Apostichopus japonicus) pond
polyculture in Dalian, Liaoning Province, China. Abstracts. Workshop on advances in sea cucumber
aquaculture and Management (ASCAM).
De Paco C, Hurtado M, MacFarland C, Martinez P, Reck G. and Richmond R. (1993). Evaluación de la
Pesquería de pepinos de mar en las Islas Galápagos - UICN. Ecuador. Unpublished report.
Guzmán H. and Guevara C. (2002). Population Structure, distribution and abundance of three commercial
species of sea cucumber (Echinodermata) in Panama. Caribbean Journal of Science 38(3-4):230–238.
Hamel J.F, Ycaza R. and Mercier A. (2003). Larval development and juvenile growth of the Galapagos sea
cucumber Isostichopus fuscus. SPC Beche de mer Information Bulletin 18.
Herrero Pérezrul M.D, Reyes Bonilla H, García Domínguez F. and Cintra-Buenrostro C.E. (1999). Reproduction and growth of Isostichopus fuscus (Echinodermata: Holothuroidea) in the southern Gulf of
California Mexico. Marine Biology 135:521-532
Hickman C.P. (1998). A Field Guide to Sea Stars and other Equinoderms of Galapagos. Galapagos
Marine Life Series. Sugar Spring Press, Lexington, Virginia, USA, 83pp.
Murillo J.C, Martínez P, Toral M. V. and Hearn A. (2003). Pepino de mar. In: Danulat, E. and Edgar, G.J.,
eds. (2003). Reserva Marina de Galápagos: Línea Base de la Biodiversidad. Fundación Charles
Darwin/Servicio Parque Nacional Galápagos, Galapagos, Ecuador.
Sant, G. (1995). Marine Invertebrates of the South Pacific: and examination of the trade. TRAFFIC
International, UK.
Wijnstekers, W. (2001) The Evolution of CITES, 6th edn. CITES Secretariat, Geneva, Switzerland.
Willock, A. (2002). Uncharted Waters. Implementation issues and potential benefits of listing
Toothfish in Appendix II of CITES. TRAFFIC International, Cambridge.
Willock, A, Burgener, M. and Sancho, A. (in prep.). First Choice or Fallback? An examination of issues
relating to the application of Appendix III of CITES to marine species. TRAFFIC.
120
FOOTNOTES
1
The information in this section is adapted from Willock et al. in prep
2
Hookah is the name given to the system whereby an air compressor pumps air to the diver via a length of
hose.
3
AIM is the decision-making body for the Galapagos Marine Reserve.
4
Range States are, from North to South, Mexico, Guatemala, El Salvador, Honduras, Nicaragua, Costa Rica,
Panama, Colombia, Ecuador and possibly Peru.
5
Captive-bred specimens, for CITES purposes, must be shown to be offspring born or otherwise produced
in a controlled environment from parents that reproduced in a controlled environment. A controlled environment is one that humans manipulate for the purpose of producing a species and that has boundaries to prevent
the entering or leaving of animals, eggs or gametes. The parental breeding stock must be established in a
manner that poses no threat to their wild populations. The stock must also be maintained regularly without
augmentation from the wild and managed in a manner designed to maintain the stock indefinitely and which has
been demonstrated to be capable of reliably producing second-generation offspring (Sant, 1995). Where an
animal has been born in captivity but does not necessarily meet the requirements of captive breeding its source
code within CITES records is “F”. The source codes for “ranching” is “R”, captive breeding is “C” and
specimens taken from the wild “W”.
6
Non-detriment findings are required at the species specific level and CITES documents should use species
names.
121
NATIONAL REPORT – CHINA
Lu Xiaoping1 and He Jianxiang2
1
CITES Management Authority of China,
Fishery Bureau, Ministry of Agriculture, P.R. China
2
1. Information on wild populations
A total of 43 species of sea cucumbers in the families Holothuridae and Stichopedidae has been described in the
Chinese waters, of which 9 are wildly regarded as the edible sea cucumbers and therefore become the major
harvest targets (Appendix I). These 9 species could be regarded as major commercial species in China. Five of
these 9 species belong to the family of Holothuridae, and are distributed in the South waters; while the other 4
species belong to the family of Stichopodidae, and are also mostly found in the South waters, but Apostichopus
japonicus (or Stichopus japonicus) is mainly found in the coast areas of the Bohai Sea and the Yellow Sea up to
the northern China.
Since China is in the dramatic change and fast growing stage in terms of economic reform and development, the
situation of the resource of sea cucumber and its administrative conservation is really connected with many various
different areas, such as the construction of the system of laws and regulations on the fishery resources, specific
national technical standard change and upgraded etc. Although some preliminary investigations and researches on
the distribution and species identification of sea cucumbers have been conducted by some institutes for aquatic
product sciences, no any intensive and/or comprehensive survey or assessment on the resource of sea cucumbers
have been done in China.
2. Nature of sea cucumber fisheries
a. Types of landing & fisheries
China has a long history to harvest the sea cucumber for food; however, no systematic statistics data are available
to sketch the sea cucumber fishery situation in China. Based on the incomplete statistics, nationally, a amount of
sea cucumber fishery industry is estimated to about 50 tons in 2000, 20 tons in 2001, 10 tons in 2002, and under
5 tons in 2003 (Table 1). Major harvested species are Stichopus spp. & Apostichopus japonicus. The above
statistics should be regarded as commercial sea cucumber fishery landings. None of other available information
could be taken as references to illustrate the scale of sea cucumber landings for the purpose of artisanal or
subsistence by local fishermen, but general understanding to the costal area development, the amount of such
nature of sea cucumber harvest have less value to be considered while set up the policy for conservation.
Table1. Yearly Natural Harvest Volume
Year
Natural Harvesting (tn.)
2000
50
2001
20
2002
10
2003
5 (lower)
122
b. Types of harvest methods
The major method to catch the sea cucumber in China is by diving, some of the by diving people directly, and
some others use diving boat with about 4 to 5 submarine inside. In the area where the sea bed is quiet flat, small
steamboat (also called as sea cucumber harrow) with dragnet could be used for sea cucumber landing, the
important condition is that this practice should happen under good weather, as the sea cucumbers normally search
for food in upside standing position, it is easier to catch them inside the dragnet.
c. Harvest seasons
The first harvest season comes to the spring, most of days in April and May. The products from this season are
normally called Spring-Cumber. Fall, from the beginning of October to the mid of December, is the second
harvest season, and the landings from this season are normally called Fall-Cucumber. The quality of SpringCucumber is better than that of Fall-Cucumber. The harvest seasons are formed through the history, and further
strengthened by the consideration of conservation. It mainly related with breeding season in summer and some
sea cucumber species have the habit of aestivation.Another recommendation comes out from the above consideration
is to stop the spring harvest if the harvest amount goes down year by year. This can provide more time for sea
cucumbers to grow and let more sea cucumbers join the breeding so that the fall harvest could get a balance in
term of total landings.
d. Sea cucumber conservation
i) Laws and Regulations
♦ None of any species of sea cucumbers have been included in the list of species under national key protection,
in other words, at the national level, the Wild Animal Protection Law (WAPL, 1989) have no measure to
control either harvest or trade activities of sea cucumbers.
♦ However, the Fishery Act (1986, modified in 2000), Fishery Licences and Permit Administrative
Regulation (FLPAR, 2002) do require some kinds of limitations on the sea cucumber harvesting. The
harvest permit could be applied from the competent fishery department at and above the county level, and in
addition to that the system of issuing person is also established to strengthen the permit administration, it
make the permit issuing person some additional obligations to monitor and regulate the fishery activities, and
make the units where issuing person gets authority more serious in monitoring the issuing person’s behaviours.
Whenever the case of exceed authority happened, the unit should get punishment accordingly besides to the
punishment on the issuing person himself. But both of these permit and system of issuing person are generally
towards to the management of common fishery, there is no special request to the sea cucumber conservation.
In addition to the above, the different types of fishery boats and to where these boats could start fishery production
activities are all subject to the permit management system. Fishery department will grant the permit in accordance
with indicators previously set up by the competent authority. The net will be used by the boat need to be inspected
and subject to separate permit too.
♦ Ocean Environment Protection Law (OEPL, 1982) provides some protections on the habitat of the sea
cucumbers, although there are no specific provisions towards to protections of sea cucumbers. The general
environment protection will benefit all marine species in those waters.
♦ Enforcement Regulations on Aquatic Wildlife Species’ Protection (ERAWSP, 1993) provides the
guidance to local governments to promulgate the more strict measures to protect the sea cucumbers. Hebei
123
provincial government and Qingdao city government published the local policy to .set up limitations towards
to wild sea cucumbers harvest, and encourage wild the sea cucumber harvest only for the use to produce
more hatchlings so that eventually could help the development of the farming and culture industry.
♦ Marine Fishery Management Regulation of Qingdao (1997) is one of above-mentioned
local policy; Article 16 states that to collect the natural resources of sea cucumbers, abalone and
agar etc, subject to the approval from competent fishery department and the collection permit
should be obtained in prior.
♦ Local key protected wildlife species list is the other document mentioned above. Apostichopus
japonicus was included in this list after 1995. It becomes the species into wildlife and changes
the legal status of this species from a major fishery species under the regulation of the Fishery Act
into a wildlife species which are mainly managed by the WAPL. All activities like catch in the
province, breeding, transportation, exploration etc., shall be under the management set forth for
all other key protected wildlife species. To catch this species in Hebei province, the fishery permit
issued by the fishery department have to be obtained, other permits for breeding, transportation
and utilization are all also required.
ii) Artificial proliferation and releasing program
The Fishery Act (modified in 2000) clearly requests that fishery departments should conduct relevant measures
to proliferate the fishery resources. And the following FLPAR issued in 2002 by the Ministry of Agriculture
further states that ”Encouraging and supporting the practice of proliferation and releasing…”
The practice on the sea cucumber artificial proliferation and set free back to the ocean program started in
1970s in Liaoning province. During the period from 1990 to1995, Shandong province established one
demonstration area of sea cucumber artificial proliferation and released them to the ocean. The size of this
demonstration area is 23 ha., about 10,000,000 hatchlings with the size around 2-3 cm have been released
back to the ocean.
In accordance with relevant statistics, from 1999 to 2002, a total of about 18.5 billion of hatchlings have been
released back to the sea. The most recently program was conducted by the Hebei provincial fishery department
in July of 2002, and 100 thousands of 2-3 cm hatchlings were released to the sea. Up to now, a total of about
more than decades of thousands of hectors have already been selected as areas for the sea cucumber hatching
and releasing program, and the proliferation numbers of about 1000 millions could be used to recover the wild
population, for a better ecological living environment and also much stronger potentials for fishery activities in
the future.
iii)
Other conservation measures employed
♦ Summer fishery moratorium: From the year of 1995, China started to conduct summer fishery
moratorium policy, and the marine area of the Yellow Sea, East China Sea and South China Sea are
all covered in this program. Including sea cucumber catch or harvest, no fishery activities could be
allowed in the above sea areas.
♦ Zero increase & negative increase program: Started from the year of 1999, China fishery policy
request the zero increase and negative increase in the marine fishery production. This policy seriously
decreases the pressure caused by human production activities. It is not only to protect marine resource,
124
but also to be a sort of measures to encourage marine culture growing up to be one of the major
fishery industry types.
♦ Fishermen transformation: This is to encourage the fishermen to change their daily life from marine
collection or harvest to the marine culture collection, to connect with local economy’s transformation,
and to well incorporate the fisherman’s future into the whole society transform plan. Some fishermen
could be transferred to other professional works, like workers, farmers or even businessman. This
program is a kind of support measure to the Zero increase policy described in above.
e. Sea cucumber farming
The sea cucumber farming mainly develops along the costal areas of Bohai Sea and Yellow Sea. The major
farmed species are Apostichopus japonicus and other Stichopus species. There almost are no sea cucumber
farming activities along the costal areas of south waters of China. The effort to develop hatchery techniques for the
marine-culture on Apostichopus japonicus started from 1954, the break through progress achieved in 1985 by
the Liaoning Provincial Oceanic & Water Products Research Institute. Around 200-400 thousands hatchlings
could be produced in per cubic meters of salt water, almost half of them can survive. For the time being, the
hatchery techniques of Apostichopus japonicus have started to be used to support the farming industry, and the
hatchling field size is about 500 thousands of square meters. According to some incomplete surveys, three provinces
including, Liaoning, Shandong and Hebei, produced about 1.2-1.5 billions of commercial hatchlings of 1 cm in
length in recent years.
The sea cucumber farming mainly happens in those of cofferdams, shallow beaches and shrimp ponds. The
operation cost is pretty low if the risk of diseases and stealing etc. won’t be counted.
The major sea cucumber farming activities started from 1980’s, along with the break through progress achieved
in hatchery techniques, the scale of the farming is growing up steadily. The statistics for these past years could tell
something in the direction of the industry (Table 2). The culture area is up to 190,000 mu in the year of 2000 and
the sea cucumber yield is 32,000 T; for the year of 2001, the culture area is 280,000 mu and the annual yield is
50,000 T; to the next year of 2002, the area increased to the 400,000 mu and the yield for this year is about
70,000 T.
Table 2. Sea Cucumbers Culture & Natural Harvesting
Year
2003
2002
2001
2000
Sea Cucumber Culture Area
(Chinese Acre)
Annual Yielding
(tn.)
400,000
280,000
190,000
70,000
50,000
32,000
Natural Harvesting
(tn.)
5
10
20
50
* acres devoted to culturing and the annual yield of cultured sea cucumbers increased between 20002003, while the levels of wild harvest have declined over this period
125
The farmed sea cucumber output exceed the natural harvesting, the development in artificial proliferation and
culture have step by step to use the cultured specimens to replace the natural harvested specimens for human
consumption, it infinitely softens pressures created by human on wild populations of sea cucumbers. In the meantime,
fishery departments become very helpful to the local economy by providing the necessary scientific guidance and
technical services. Sea cucumber farming already becomes the new economic increase point and it does help
both in promotion on life of local fishermen and the conservation of sea cucumbers in the wild. For example, there
are more than 100 families are specializing sea cucumbers farming in the small town of Chang Xing Island,
WaFangDian city, Liaoning province. More than 3000 people are employed in this industry and the annual
income of these families could be high up to 2 million RMB (is about 250,000 USD) ; Another example is WeiHai
city of Shandong province, the city promulgated a policy to support the sea cucumber farming industry. It provisions
that “any of units or individuals would like to be involved sea cucumber farming in tidal zone shrimp pond and the
area bigger than 100 mu, the city will provide additional funds in a certain rate connect with 50% of the total
investment to support, and the owner will get some taxes exemption”. Till now, in this city, more than 350 families
have invested their money and energy into 6000 mu shrimp ponds for sea cucumber culture, the annual production
value has reached to about 0.24 billion RMB (30,000,000 USD), and the average of family annual income is
about 686,000 RMB (80,000 USD)
f. Preferred markets and most important uses
Domestic markets are major and preferred markets of sea cucumbers in China, among various of use of sea
cucumber, more than 85% of sea cucumbers will be used as human’s delicacy. For the reason of transportation
and reserve, the major part of this type of consumption is mainly from the dried sea cucumbers. Water soaked sea
cucumbers with low quality both in species and taste are frequently sold in most of free markets. Fresh sea
cucumbers can also be used for dishes, but it is very rare and very difficult to reserve. Other 15% is used as
ingredients of medicines, tonic stuff and other products. Again, the dried sea cucumber is the major form being
utilized in China.
3. Domestic and international trade
g. Domestic trade
While in the section 2.e., the data on the growing up of farming activities and economy income of operation
involved in sea cucumber farming provided a good explanation to the levels of domestic consumption and trade
trends. It’s almost impossible to give a price list by species, however, the commodity in different type reference
price could sketch a little of understandings to the price of sea cucumber and its products (Table 3).
From dried sea cucumbers to other products, all seem very expensive, no matter what origin they are. The
foodstuff in the restaurant could be very high but too many factors such as waiter’s attitude, cook skill of chef,
eating environment etc, involved in that price setting up, the price quoted from restaurant should not be taken as
the reference of the marketing price.
126
Table 3. Price information quoted for reference
Products & Origin
Dried SC from Cheli
Light dried SC in Shandong
Half dried SC in Dalian, Liaoning
Standard
3-7 cm
100-160 individuals per
kg
50 individuals per kg
Salty SC in Dalian, Liaoning
40 individual per kg
Branded dried SC in Dalian, No information
Liaoning
HaiYanTang in Dalian, Liaoning
HaiYanTang: SC Nutriment
Price
23.3 USD
3800 RMB (459
USD)
700 RMB (85
USD)
440 RMB (53
USD)
Under negotiation
Units
Kg
Kg
Kg
Kg
Kg
Fine packing, 18 g
496 RMB (60 Packing
USD)
HaiYanTang: SC Nutriment
Fine packing, 24 g
868 RMB (105 Packing
USD)
HaiYanTang: SC Nutriment
Common packing, 9 g
198 RMB (24 Packing
USD)
HaiYanTang: SC Nutriment
Common packing, 18 g 396 RMB (48 Packing
USD)
HaiYanTang: SC Nutriment
Common packing, 19.2 420 RMB (51 Packing
g
USD)
260 RMB (31 Box
SC oral liq. in Changdao, 6 bottles in 1 box
USD)
Shandong
106 RMB (13 Box
*XinYiDai
SC,in
Qingdao, 1 box, 150 g
USD)
Shandong
Sun Dragon SC can in Qingdao, 4 can in 1 present 168 RMB (20 Packing
USD)
packing
Shandong
In present packing
863 RMB (104 Packing
OuShenBao SC living ingredients
USD)
* Using the US techniques produced in Qingdao, Shandong province.
h. International trade
The information on the international trade of sea cucumbers (rock, dried, salted) could provide some hints to the
degree or the level of the international trade of these species. From the data showing in the below tables and
charts, ggenerally, China is a country import more sea cucumbers than its export, no matter we use the volume or
the value as the factor to make analysis. From the data listed below, there is not a clear trend in directions, but for
the importation, the cost seems going up steadily and the volume seems going up for a long term. There is not a
trend could be referred from the data for these years. The reason for the difficulties while to analysis could be lack
of enough information; the following studies will provide more information for this area.
127
Table 4. Sea Cucumbers Import and Export
Year
Volume
(kg)
139,152
186,234
2,058,574
481,092
1,619,079
4,484,131
1999
2000
2001
2002
2003
Total
Import
Value
(usd)
265,306
793,045
1,229,090
1,281,770
3,459,259
7,028,470
Average
(usd/kg)
1.91
4.26
0.60
2.66
2.14
Volume
(kg)
87,919
298,479
653,487
581,237
152,323
1,773,445
Export
Value
(usd)
208,872
612,301
845,137
519,203
243,976
2,429,489
Average
(usd/kg)
2.38
2.05
1.29
0.89
1.60
Chart 1: The Sea Cucumber importation
3,500,000
3,000,000
2,500,000
2,000,000
1,500,000
1,000,000
500,000
0
1999
2000
2001
2002
Sea cucumber import volum (kg)
2003
Value (usd)
Chart 1 &2 on the importation and exportation of sea cucumbers showing some results that is a little confused to
us generally. The potential reason could be the change of price in the international market, the trend in Chart 1
seems support this explanation, but the chart 2 does not. Other reasons will be too many even need to review the
validity of the information kept in the Customs.
Chart 2 The Sea Cucumber exportation
1,000,000
800,000
600,000
400,000
200,000
0
1999
2000
2001
Sea cucumber export volum (kg)
128
2002
Value (usd)
2003
From the Appendix II and III, the list of county of origins included 34 counties and/or territories, while the
destined countries and/or territories for the export of sea cucumber are only about 15 countries. From which, the
data of import and export have been included at the annual bases for reference.
I. Others
The information requested in this section is normally for those species already listed in the CITES appendices. The
sea cucumber species have not been listed into the CITES and have not been included in the wildlife protection list
of China. Mainly regulated by the Fishery Act, having very little connection with wild animal protection law,
therefor, the information provided in this section is mostly based on the personal analysis, more substantial information
collected through formal governmental channels will be provided in the future.
♦ There is no any trade controls at all, since no limitation nationally applied towards to the trade of sea cucumbers,
there is no need to establish a team or to use the existed enforcement power to regulate the trade of these
resources.
♦ The identification of specimens in trade is not for regulation, but to tell the difference for the inspection of
products. There is not a comprehensive identification manual at all, mostly based on the common knowledge
to the commerce, the relation established between the commerce and species normally is based on the area
and its common production either by wild caught or from the sea cucumbers farming operations.
♦ Information regarding the illegal trade of sea cucumbers in China is currently not available. The reasons could
be various, such as lack of understanding to the limitations set up by the authority, lack of power to check
fisherman with sea cucumbers whether they get permit or not, sea cucumber species will not encounter any
law enforcement (except for Hebei province) problems as if the authority cannot stop the illegal catch around
the costal line; there is no any control on the sales in markets and to the restaurant. All of possible reasons are
personal analysis; none of them could be confirmed by any sense at this time.
REFERENCES
Chen Jiaxin. 2003. Present Status and Prospects of Sea Cucumber Industry in China. Yellow Sea Fisheries
Research Institute.
Committee of Natural Resources of China. 1995. Series of Natural Resources of China: Fisheries. Publishing
House of Environmental Sciences of China.
Huang Zhongguo. 1994. Oceanic Species and Distribution in China. Ocean Press.
Fishery Bureau of Ministry of Agriculture. 2000. CHINA FISHERIES YEARBOOK. Publishing House of
Chinese Agriculture.
Fishery Bureau of Ministry of Agriculture. 2001. CHINA FISHERIES YEARBOOK. Publishing House of
Chinese Agriculture.
Fishery Bureau of Ministry of Agriculture. 2002. CHINA FISHERIES YEARBOOK. Publishing House of
Chinese Agriculture.
129
Annex I: Species List of Sea Cucumbers in the families of Holothuridae & Stichopus In China
Latin Name
Distribution area
Bohadschia marmorata Jaeger
Dazhou island of Hainan, Xisha & Nansha
B. bivittata, B. koellikeri
Bohadschia argus Jaeger
Xisha, Nansha islands
Bohadschia graeffei (Semper)
Nansha islands
Actinopyga lecanora (Jaeger)
Xisha, Nansha islands
Actinopyga echinites (Jaeger)
Sanya, Xisha, Baoan and Aotou county of Guangdong
Actinopyga mauritiana (Quoy et Gaimard)
South of Hainan, Xisha & Nansha
Actinopyga miliaris (Quoy et Gaimard)
Xisha
Labidodemas semperianum Selenka
YongXing island of Xisha & Nansha
Holothuria moebi Ludwig
Middle and south costal area of Guangdong & south of Hainan
Holothuria cinerascens (Brandt)
YongXing island of Xisha & Hainan
Halodeima atra
Holothuria flavomaculata Semper
Tidle zone of Sanya, Hainan
Holothuria atra Jaeger
Hainan, Xisha & Nansha
Halodeima atra
Holothuria edulis Lesson
South of Hainan
Halodeima edulis
Holothuria dicrepans Semper
Yongxing island of Xisha
Holothuria olivacea Ludwig
Yongxing island of Xisha
Holothuria difficilis Semper
Xisha, south of Hainan, Taiwan & Nansha
Microthele difficilis
Holothuria impatiens (Forskaal)
Xisha, Hainan & Nansha
Holothuria arenicola Semper
Xisha
Holothuria gracilis Semper
South of Hainan
Holothuria hilla Lesson
Xisha, Nansha & Hainan
Holothuria monacaria
Holothuria leucospilota (Brandt)
Xisha, Hainan & Guangdong
Holothuria vagabunda
Holothuria fuscocinerea Jaeger
Xisha, Hainan; Baoan county & Daya Bay of Guangdong
Holothuria pervicax Selenka
Xisha, south of Hainan
Holothuria dietrichi Ludwig
HongKong
Holothuria pardalis Selenka
Xisha, Hainan
Holothuria verrucosa Selenka
Xisha
Holothuria multipilula Liao
Xisha
Holothuria rigida Selenka
Yongxing island of Xisha
Holothuria inhabilis Selenka
Xisha
Holothuria spinifera Théel
Xisha
Holothuria ocellata Jaeger
Northern bay, south of Hainan, Nansha & peral river estuary
130
Annex I (continued)
Latin Name
Distribution area
Holothuria scabra Jaeger
Xisha, Hainan, west coast of Guangdong
Holothuria albiventer Semper
South of Hainan
Holothuria martensi Semper
Northern bay
Holothuria nobilis (Selenka)
Xisha & south of Hainan
Microthele nobilis
Holothuria axiologa H.L. Clark
STICHOPODIDAE – 7 Species
Xisha
Latin Name
Distribution area
Stichopus chloronotus Brandt
Stichopus variegatus Semper
Xisha & south of Hainan, edible
Northern bay, Xisha, Nansha, Hainan & Leizhou peninsular.
Edible
Stichopus horrens Selenka
Xisha, Nansha & Hainan
Stichopus flaccus Liao
Apostichopus japonicus (Selenka )
Middle and west part of Northern bay
Costal area of Bohai Sea & Yellow Sea, the best of edible
stichopus japonicus
cucumber
Thelenota ananas (Jaeger)
Xisha & Nansha, high quality edible cucumber
Thelenota anax H.L. Clark
Xisha
131
Annex II: List of Country & territory of origin - annual import volume & value (total 34 )
Year
1999
2000
2002
2001
1999
1999
2000
2001
2002
2003
2001
2002
2000
2003
1999
2001
2002
2003
2003
2001
1999
2000
2001
2002
2003
1999
2000
2001
2002
2003
1999
2001
2002
2003
1999
2000
2001
2002
2002
2003
2002
2003
Country / territory
Australia
Belgium
Burma
Canda
Chile
Cuba
Ecuador
Egypt
Guinea
HongKong SAR
Indonesia
Japan
Madagascar
Malaysia
Maldives
New Zeland
import volume (kg)
58
629
1,209
15
2,000
14,630
28,426
17,541
16,629
142,359
1,200
5,904
1,881
700
91
1,160
8,465
8,430
210
624
50,187
13,760
13,500
2,600
17,680
9,120
44,062
1,145,943
279,758
605,589
14,275
20
256
29,637
7,189
10,581
940
5,575
595
505
11,475
10,625
132
import value (usd)
294
4,403
2,053
67
2,892
22,107
81,361
41,385
114,008
515,489
720
3,554
41,382
13,300
525
11,258
108,089
123,176
4,213
4,992
154,001
54,509
11,369
6,208
21,536
4,766
84,846
487,793
499,035
677,791
19,795
1,023
5,232
389,732
13,793
24,031
2,560
18,422
14,862
8,392
11,475
14,391
Year
Country / territory
import volume (kg)
import value (usd)
1999
N orth K orea
55
1,300
2001
234
2,808
2002
537
11,782
2003
25
750
Pakistan
302
1,363
2001
Papua New G uinea
225
1,327
2002
Peru
700
4,332
5,520
4,429
Philippines
28,803
23,599
2000
45,017
348,241
2001
791,482
489,250
2002
63,371
251,969
2003
142,765
254,990
500
7,500
2000
850
8,500
2001
1,200
6,000
2002
2003
1999
1999
R ussia Federation
2003
1999
Singapore
2000
2002
2001
South A frica
2002
2000
South K orea
5,169
265,652
568
1,776
905
2,940
80
967
1,076
1,642
10,211
10,211
12,340
76,766
2001
21,096
107,840
2002
6,470
32,448
2003
1999
Spain
2002
5,900
29,589
2,190
2,609
8,496
16,994
2003
Sri Lanka
324
7,376
2002
T aiwan province
1,496
3,106
567,809
690,700
2003
2000
T anzania
200
154
2002
10,805
10,633
2003
22,565
27,530
55,910
18,780
2001
T hailand
2002
4,050
1,557
T urkey
2,100
10,532
1,800
9,000
U SA
9,473
10,293
2000
27,172
65,397
2001
6,408
40,276
2002
37,533
140,463
2003
46,282
389,602
2002
2003
1999
2000
V iet N am
200
346
2002
2,475
2,475
2003
5,185
11,621
211
169
2000
Fiji
133
Annex III: List of destined countries/territories - annual export volume & value (total 15 )
Year
2002
2003
2001
1999
2000
2002
1999
2000
2001
2002
2003
1999
2000
2001
2002
2003
2003
2000
2003
2001
2002
2003
1999
2000
2003
1999
2000
2001
2002
2003
2001
2002
2003
2000
2003
1999
2000
Country/territory
Australia
Import volume (kg)
885
3,660
Belgium
750
5,100
Canada
629
Finland
60
HongKong SAR
22,330
26,342
13,039
12,077
7,588
Japan
1,235
200
131
48
181
Macao SAR
280
Malaysia
15
Russian Federation 168
150
230
Singapore
10
80
5
South Korea
59,234
265,951
639,359
567,817
140,115
Sudan
40
200
200
Taiwan province
5,252
64
USA
10
Zimbabwe
10
134
import value (usd)
3,275
3,660
1,906
27,550
5,032
300
64,442
82,148
54,958
49,038
23,533
3,266
6,750
327
244
25,855
564
114
28
393
600
820
400
103
10
113,134
511,650
785,345
455,280
177,712
2,208
10,466
11,494
6,303
300
80
201
NATIONAL REPORT –
HONG KONG SPECIAL ADMINISTRATIVE REGION, CHINA
Kwan Sai-Ping and Chow Wing Kuen
Agriculture, FIsheries and Conservation Department, Hong Kong
1. Information on wild populations
Distribution and abundance of sea cucumber (also known as Bêche-de-mer) species are not well documented
in Hong Kong. However, at least, the following species have been recorded in Hong Kong waters:
Holothuria leucospilota (previous known as Holothuria vagabunda) 1, 2, 3, 4, 5
Holothuria arenicola 3
Holothuria insignis 1
Holothuria fuscocinerea 1
Holothuria cinerascens 1
Holothuria dietrichi 4
Holothuria impatiens 5
Polycheira rufescens 1,2,3,5
Colochirus quadrangularis 1
Pseudocolochirus violaceus 1,4
Afrocucumis africana 1
Acaudina molpadioides 1
Protankyra bidentata 1
Thyone papuensis 1
Havelockia sp. 1
Stichopus sp. 3
2. Nature of sea cucumber fisheries
No sea cucumber fishery is observed in Hong Kong waters.
3.Domestic and International trade
Hong Kong is reported as one of the major importers and re-exporters of sea cucumber 6. Among abalone,
sharkfin and fish maw, sea cucumber is regarded as a food delicacy in Chinese tradition. In Hong Kong, sea
cucumbers are mainly imported in dried form 7 even though it was also reported that specialized products are
also produced from the gonad, respiratory trees and viscera of sea cucumber 8. Sea cucumber is also traded
in aquarium trade but the trade volume and pattern are not known.
The customs data from 1999-2003 (annex 1) showed that Hong Kong imported sea cucumber from more
than 70 countries and territories all around the world. Indonesia, Philippines and Papua New Guinea were the
major exporting countries in terms of volume. The total import volume varied from 2, 992 to 4, 759 tonnes
annually.
The export data (annex 1) shows that Hong Kong export dried sea cucumber to 46 different countries and
territories. Mainland China, Vietnam, Taiwan, USA and Thailand was the top 5 destination in the year 2003.
135
The most expensive sea cucumbers observed are the ones from Japan (presumably Stichopus japonicus) and
their import price ranged from HKD 910 -1482 per kilogram while the average price of the rest sea cucumber
imported ranged from HKD 67-75 per kilogram. The retail price observed in the market in 2002 ranged from
HKD 260 -620 per catty and that of Stichopus japonicus from Japan was over HKD 2000 per catty.
Many of the sea cucumbers imported were later on re-exported elsewhere. Table 1 shows that more than a
half of the sea cucumbers were not consumed in Hong Kong. It also shows an apparent trend of declining reexport ratio from 1999-2003. This may indicate the local consumption of sea cucumber is increasing but more
precise trade studies should be carried out to verify this interpretation.
Table 1: Import and re-export volume of sea cucumber from 1999-2003
1999
2000
2001
2002
2003
Total import (kg)
2,922,332
4,758,719
4,382,272
4,417,354
4,655,496
Total re-export (kg)
2,657,502
4,221,073
3,866,623
2,943,878
2,528,543
91%
89%
88%
69%
54%
Re-export ratio
Legislations:
(1) Marine Parks Ordinance, Cap. 476
The Marine Parks Ordinance (Cap. 476) was enacted in 1995 to provide for the designation, control and
management of marine parks and marine reserves in Hong Kong. To date, there are 4 marine parks and 1
marine reserve designated in Hong Kong waters. Unauthorized fishing, hunting, collecting or possessing any
wild animals or plants, or their parts are strictly prohibited within marine parks and marine reserves. Anyone
contravenes this ordinance may lead to a fine of HKD 25, 000 and 1 year imprisonment.
(2) Animals and plants (Protection of Endangered Species) Ordinance, Cap 187
The Animals and Plants (Protection of Endangered Species) Ordinance, Cap 187 is the local legislation that
gives effect to CITES. The Schedules to the Ordinance have recently been amended to effect the changes to
CITES Appendices as adopted at the 12th Conference of the Parties to CITES. The amended Schedules,
which include the listing of Isostichopus fuscus, will take effect from mid 2004. Since then, import of Isostichopus
fuscus from Ecuador would require a CITES export permit and import from elsewhere would require a
certificate of origin. An export licence would also be required for its re-export. The maximum penalty is HKD
500, 000, 1 years of imprisonment and mandatory forfeiture of the concerned specimens.
(3) Customs declaration
The commodity code of sea cucumber (Beche-de-mer, dried, salted or in brine) is 0307 9930 under the Hong
Kong Harmonized System 9. Under the Import and Export (Registration) Regulations, every person who
imports or exports any article other than an exempted article is required to lodge an accurate and complete
import or export/re-export declaration within 14 days after the importation or exportation. Prosecution may
be initiated against any person who fails to lodge the required declaration, or knowingly or recklessly lodges
any declaration that is inaccurate in any material particular.
136
Feasibility of enforcement:
There are potential problems in enforcement work of trade control of sea cucumber. Firstly, there are a lot of
sea cucumber species. There are approximately 1200 species of sea cucumber in the world and about 300 of
these can be utilized in the dried sea cucumber trade 6. It is impossible to enforce the trade regulation if there
is no user-friendly identification method available.
Secondly, most of the sea cucumbers are traded in dried form. Some of the diagnostic characteristics would
have been destroyed in the drying process. This may make it impossible to identify the specimens to the
species level.
Lastly, specialized products produced from the gonad, respiratory trees and viscera of sea cucumber are also
traded internationally. Thus far, their trade is not yet clear and their identification is still unavailable. In light of
the above problems, it is recommended more studies should be carried out in order to sort out the above
matters. In order to generate real conservation benefits, it is recommended any regulations, including CITES
listing proposals, should consider the feasibility of enforcement thoroughly before they are imposed.
References:
1. Clark, A.M. (1980) Echinoderms of Hong Kong. In Proceeding of the First International Marine
Biological Workshop: The Marine Flora and Fauna of Hong Kong and Southern China,
Hong Kong, 1980 (Eds. B. Morton and C.K. Tseng). The Hong Kong University Press, Hong
Kong, p.485-501.
2. Hill, D.S. and K. Phillipps (1981) A Colour Guide to Hong Kong Animals, Hong Kong Government
Printer, Hong Kong.
3. Morton, B and J. Morton (1983). The seashore ecology of Hong Kong, Hong Kong University Press.
4. Huang, Z.G. (ed) (1994). Marine species and their distributions on China’s Seas, China Ocean Press,
Beijing.
5. Morton, B and E, Harper (1995) Introduction to the Cape d’Aguilar Marine Reserve, Hong Kong, Hong
Kong University Press, Hong Kong .
6. Sant, G. (1995) Marine Invertebrates of the South Pacific: An Examination of the Trade. A
TRAFFIC Network Species in Danger Report, TRAFFIC International.
7. Clarke, S. (2002) Trade in Asian Dried Seafood: Characterization, Estimation and Implications for
Conservation, Wildlife Conservation Society.
8. USA (2002) Trade in Sea Cucumbers in the Families Holothuridae and Stichopodidae. CoP12
Doc. 45.
9, Cenus and Statistics Department (2002) Hong Kong Imports and Exports Classfication List
(Harmonized System), 2002 Edition, Volume One: Commodity Section I-X, Hong Kong
Special Adminstrative Region Government, Hong Kong, China.
Remarks:
USD 1 = HKD 7.78
1 catty = 600 gram
137
Table 2. Imports of sea cucumbers.
Import
1999
Country/Territory HKD
Indonesia
Philippines
Papua N Guinea
Singapore R
Fiji
Solomon Is
Madagascar
Japan
Malaysia
Djibouti
Yemen R
Australia
USA
Thailand
Tanzania
Sri Lanka
Mozambique
Canada
Maldives R
South Africa R
Taiwan
The Mainland of
Kenya
Aust & Oceania
African Nes
Egypt Arab R
Seychelles
Tunisia
Haiti
Vanuatu
Peru
Cuba
India
Kiribati R
Vietnam
U A Emirates
Mauritius
New Zealand
Ecuador
Marshall Islands
Micronesia FS &
Turkey
Mexico
Hong Kong SAR
Chile
31,341
31,608
28,817
10,715
15,048
2,641
18,729
53,879
1,471
0
256
25,206
5,684
3,410
5,989
2,008
76
623
229
649
6,164
1,680
148
5737
0
0
0
0
0
286
879
570
928
737
957
5
12
186
1,274
0
0
0
0
0
0
2000
2001
Quantity
2002
2003
HKD '000 Quantity HKD '000 Quantity HKD Quantity HKD '000 Quantity
762,707
42,938 1,041,559
35,252 1,068,768 33,548 1,010,698
29,900 977,893
591,092
63,830 1,070,154
39,697 737,232 40,845 802,023
33,306 666,841
350,321
45,482 524,101
41,165
54,122 40,344 380,595
41,146 447,632
165,911
18,531 284,804
16,583 249,278 20,092 284,657
21,414 409,315
168,264
28,149 364,369
22,893 291,093 18,313 235,503
16,150 264,253
49,737
7,646 149,115
14,896 259,727 12,027 248,751
7,438 222,763
166,364
17,745 178,392
17,529 194,129 14,217 193,551
8,821 216,354
58,343
81,952
75,528 100,602 110,558 147,874 137,999 305,792 206,359
19,854
4,617
67,975
4,090
73,158 10,276 144,754
10,657 147,523
0
0
0
0
1
567
4,133
5,012 134,999
3,287
0
0
798
4,848 10,454 102,414
15,266 134,919
125,289
43,646 146,524
41,282 185,952 30,964 124,665
35,416 118,827
112,283
8,311 170,423
4,964
88,816 10,251 154,837
9,074 113,119
60,331
12,492 133,858
9,695 101,020 7,329
78,528
4,552
69,207
41,352
8,930 118,166
4,676
56,382 5,462
91,672
3,662
67,555
21,381
3,647
53,867
1,964
33,288 3,610
54,523
3,836
64,972
500
40
109
197
853 3,307
37,000
5,210
63,363
4,883
2,242
13,837
3,332
58,541 1,363
17,861
4,533
60,506
4,170
2,780
53,915
1,563
27,928 1,080
37,829
2,451
49,013
10,149
2,188
27,876
1,274
30,178 1,119
53,792
620
37,800
40,958
6,606
37,830
6,360
40,143 5,545
40,800
5,187
34,570
25,020
2,395
14,946
451
4,031
898
37,400
1,830
30,657
1,707
3,377
51,580
1,407
39,444 1,873
20,429
4,235
22,658
32294
3822
24227
6515
37574
4300
22558
4456
21256
0
0
0
0
0
144
2,340
1,417
19,977
0
102
677
0
0
961
6,510
2,496
17,220
0
1,309
7,121
2,142
15,678
681
5,662
3,412
13,028
0
0
0
0
0
0
0
622
11,300
0
0
0
0
0
242
1,000
2,362
9,680
7,966
1,315
28,467
936
16,647
460
8,363
352
9,001
4,170
1,450
7,331
1,364
3,881
185
1,828
798
8,354
2,920
3,593
19,023
3,042
13,941
904
3,800
1,862
7,648
6,610
454
1,906
930
9,810
356
2,391
1,622
5,655
6,523
683
9,073
1,556
22,774
883
8,561
694
5,528
34,093
186
600
950
3,274
142
756
637
5,415
140
983
9,100
13
256 1,159
17,141
1,065
4,508
300
271
3,185
0
0
131
667
768
3,682
530
1,664
7,583
115
317
276
1,440
305
3,471
24,567
5,769
15,285
384
991 3,983
10,130
1,414
3,026
0
0
0
0
0
0
0
757
2,739
0
0
0
0
0
335
6,368
123
2,252
0
0
0
0
0
68
1,290
106
1,995
0
68
150
758
1,818 1,339
3,302
477
1,270
0
0
0
0
0
0
0
66
874
0
486
22,318
200
7,599
85
2,906
137
527
138
Table 2. Imports of sea cucumbers (continued).
Import
1999
2000
2001
2002
2003
Country/Territory HKD
Quantity HKD '000 Quantity HKD '000 Quantity HKD Quantity HKD '000 Quantity
Korea R
0
0
0
0
0
0
29
651
45
510
Tonga
0
0
0
0
0
0
0
0
180
296
Korea Dem P R
0
0
0
0
0
0
0
0
373
284
Nicaragua
0
0
0
0
0
0
0
0
111
252
Sao Tome And
0
0
0
0
0
0
0
0
23
202
Asian Nes
0
0
0
0
0
0
0
0
20
96
Dominican R
0
0
0
0
0
0
54
2,562
4
45
Costa Rica
29
108
254
664
41
325
0
0
4
7
Yugoslavia F R
0
0
0
0
0
0
80
200
0
0
Netherlands
0
0
0
0
2
8
0
0
0
0
France
0
0
0
0
20
155
0
0
0
0
Brazil
0
0
0
0
42
444
10
50
0
0
Spain
0
0
211
1,000
0
0
0
0
0
0
Colombia
0
0
0
0
35
540
0
0
0
0
Puerto Rico
0
0
0
0
0
0
56
1,300
0
0
Oman
60
180
146
960
93
490
161
507
0
0
Saudi Arabia
72
782
0
0
5
30
0
0
Macao
0
0
0
0
20
1,200
0
0
0
0
Morocco
0
0
0
0
447
7,438
205
1,932
0
0
Somali Dem R
0
0
0
0
0
0
702
3,835
0
0
Comoros
0
0
62
600
0
0
0
0
0
0
Mauitania
0
0
0
0
0
0
146
1,860
0
0
Senegal
0
0
0
0
0
0
189
3,000
0
0
Swaziland
0
0
83
354
0
0
0
0
0
0
US Oceania
1,789
11,528
1,935
17,623
3,019
40,622
0
0
0
0
W Samoa
533
5,718
0
0
0
0
0
0
0
0
Total
260,422 2,922,332 432,666 4,758,719 393,292 4,382,272 439,628 4,417,354 602,212 4,655,496
139
Table 3. Reexports
Re-export
HS code: 0307 9930 Beche-de-mer, dried, salted or in brine (KG)
1999
Country/Territory of
HKD '000
consignment
China
Vietnam
Taiwan
USA
78,159
2000
Quantity
(kg)
HKD '000
2,268,382
176,034
2001
Quantity
(kg)
HKD '000
3,770,695
141,171
2002
2003
Quantity
(kg)
HKD
'000
Quantity
(kg)
HKD
'000
Quantity
(kg)
3,542,713
73,903
2,126,617
56,700
2,034,399
240,870
0
0
0
0
0
0
13,097
439,233
8,695
15,479
158,408
25,164
208,791
9,927
117,081
16,662
152,440
9,229
81,761
2,544
16,775
2,880
22,677
2,750
37,799
6,409
105,765
13,847
72,138
Thailand
5,265
31,025
6,005
29,864
6,555
39,652
7,656
39,798
5,482
25,173
Korea R
4,780
50,178
7,102
81,900
4,294
62,211
2,703
35,728
1,886
23,788
Canada
2,722
16,362
2,717
12,960
3,395
27,210
3,906
14,491
3,116
21,543
12,293
80,820
9,854
70,054
6,122
28,474
4,253
18,820
4,457
19,457
Malaysia
2,550
21,918
2,866
21,347
667
5,583
1,046
5,839
956
4,545
Australia
288
2,559
79
570
359
1,920
203
1,506
258
2,902
Singapore R
Sri Lanka
Japan
Korea Dem P R
Spain
0
0
0
0
0
0
38
808
91
1,403
46
147
711
833
325
521
213
1,243
530
519
644
750
0
0
94
50
0
0
10
20
0
0
0
0
46
1,026
0
0
21
15
10
Trinidad & Tobago
0
0
0
0
0
0
0
0
1
Switzerland
0
0
13
15
39
16
0
0
0
0
Portugal
Germany F R
0
0
42
19
28
10
56
20
0
0
3
4
6
8
0
0
67
25
0
0
France
0
1
0
0
28
10
0
0
0
0
Italy
28
10
28
12
39
14
0
0
0
0
Rep of Ireland
0
0
0
0
27
60
0
0
0
0
Macedonia R
0
0
0
0
0
0
14
5
0
0
Kazakhstan R
0
0
0
0
28
10
28
29
0
0
Ukraine
0
0
0
0
0
0
28
20
0
0
Brazil
0
0
0
0
70
250
63
25
0
0
Panama R
0
0
0
0
9
23
0
0
0
0
Venezuela
0
0
0
0
126
45
0
0
0
0
Syrian Arab R
0
0
0
0
28
10
0
0
0
0
Romania
0
0
54
60
0
0
0
0
0
0
Russian f
0
0
11
12
0
0
0
0
0
0
Costa Rica
0
0
26
478
0
0
0
0
0
0
Turkey
8
42
0
0
0
0
0
0
0
0
Poland
22
24
0
0
0
0
0
0
0
0
Israel
13
6
14
5
0
0
0
0
0
0
236
10,080
13
129
0
0
0
0
0
0
0
0
188
594
586
1,905
7
8
0
0
Indonesia
Macao
Philippines
0
0
0
0
0
0
150
1,428
0
0
Pakistan
0
0
1
1
0
0
0
0
0
0
India
0
0
56
38
0
0
0
0
0
0
Brunei
0
0
0
0
38
15
0
0
0
0
Bangladesh
0
0
0
0
45
20
0
0
Mali
0
0
0
0
28
10
0
0
0
0
Algeria
0
0
10
5
0
0
0
0
0
0
Djibouti
New Zealand
Nepal
TOTAL
0
0
11
6
0
0
0
0
0
0
19
11
0
0
0
0
0
0
0
0
0
0
0
0
13
5
28
10
125,098 2,657,502
233,886 4,221,073
140
176,789 3,866,623 130,574 2,943,878 105,280 2,528,543
NATIONAL REPORT – CUBA
Irma Alfonso Hernandez
Fisheries Research Center, CUBA
1. Information on wild populations
a) Commercial Species:
STICHOPODIDAE
There are 32 species of sea cucumber reported on Cuban waters but only one of these Isostichopus badionotus
has been commercially fished in Cuba from 1999.
Non-commercial species:
STICHOPODIDAE
Astichopus multifidus
HOLOTHURIIDAE
Actinopyga agassizii
H. floridana
H. mexicana
H. cubana
H. grisea
H. thomasi
H. impatiens
H. princeps
H. glaberrima
H. arenicola
H. surinamensis
b) Area of distribution and habitats.
- I. badionotus is distributed all around the Cuban shelf in mouth-sandy and sand-slushy bottoms.
- A. agassizii, H. floridana and H. grisea (under stones, the last) are distributed in north central coast of
Cuba. They are also present but scarce at southern region.
- H. mexicana and A. multifidus, are well distributed around the island.
- H. thomasi is reported only for the south western region, located on sandy bottom.
- H. arenicola (under stones) highest abundance at south-central Cuban region.
141
c) Abundance
I. badionotus, The highest abundances (0 up to 8 800 /ha) are located at southeastern region and also
in some bays of the northeastern region of the island. A. agassizi (to 1 800/ha), H. floridana (to 2
800/ha) in the north central Cuban region. H. mexicana (to 17 000/ha) and A. multifidus (to 6 300/
ha). H.grisea (under stones, the last) with few local abundances and the rest of the species, are very
scarce in Cuba.
2. Nature of sea cucumber fisheries
a) Commercial, artisanal, subsistence : Commercial
b) Estimated number of fishers: 28 fishers and 18 proccesors
c) Type of fishing methods and gear equipment used:
Each speedboat is provided with compressed air tanks for use by the divers and four “on board tanks”
with recycled water to hold the sea cucumbers. The divers use a “narquilex” or ¨hookas¨ system with
a hose (95 m long) coupled to the compressor tank with the other end fitted with a mouthpiece. An air
regulator system is used to supply air and allow longer time under the water. The fishery is carried out
at depths between 3 to 15 meters.
d) Licensing/permitting requirements: Yes
To date I. badionotus has been captured from quotes recommended and assigned by fishery localities,
for the Fishery Research Centre, after a potential population’s assessment. A rational catch plans by
the authorities PESCACUBA, who has the control trough the OPIP (Inspection Fishery Office) from
the Fishery Industry Ministry.
e) Sea cucumber farming, if any:
Studies are underway to detemrine the feasibility of a pilot land-based hatchery
f) Preferred markets (live vs. dried):
The product is sold to NENEKA c.a., a Korean company who export this product to Hong
Kong. The average live vs. dried has been approximately 20:1.
g) Identification of the most important uses of sea cucumbers. Commercial.
To date the principal use is for commercial export. Since 2002 research has been underway to use
fishery by-products, mainly gonads and the boiled freshwater from processing, for bioactive extracts
and medicines against certain illnesses and other uses.
142
h) Landing data (species, by catch, kg, sizes, etc), if available:
Average 48 pieces/kg and 6 cm/pieces.
i) Conservation measures (minimum harvesting size, closed areas, closed seasons, etc):
Fishery regulations were established to protect the population since mid-2000, enforced by the National
Office of Fishery Inspection. The regulations also established catch’s quota for each locality, an effort
limited by each fishing campaign, a minimal legal size of 22 cm., a seasonal restriction recently extended
(June-October) to protect the reproductive season. A rule is to prevent more than 60 sea cucumbers
collected in the bag by immersion, and the maintenance of covered “on board tanks” to protect the sea
cucumbers from the sun light.
3. Domestic and International Trade
a) Information on value, retail, wholesale prices and trends.
Around dry weight 89 104 kg., have been sold. Prices have steadily increased during this period from
US$13.5/kg dry product ¨Class A¨ in 1999-2001, US$18.0 in 2001-2002 to US$20.0/kg during
December 2002 to March 2003, and US$22.0/kg during April 2003 to date as a result of improved
¨Class A¨ and ¨Class B¨ product quality. The variability in ¨Class B¨ quality prize has fluctuated between
US $6.00/kg.to US $10.00/kg on depending of others pay off.
b) Export volumes:
Year
1999
2000
2001
2002
2003
2004
Totals
Export
volumes
Value (Cuba)
Clase A
(kg dry
weight)
($ usd)
(%)
5510
31796
18234
8642
8242
5140
77564
71 630
341 718
306 708
133 186
148 634
81 529
1 083 405
17
70
80
81
83
85
143
c) Information on key sea cucumber trading countries and territories:
All the production dehydrated-salted is sold to NENEKA c.a. a Korean company.
d) Trade controls and enforcement, including identification of specimens in trade:
Authorities emit a sanitary certificate with a product quantity’s and qualities, by a customs officer
before the product send to Hong Kong.
e) Information on illegal, unreported and unregulated trade:
No illegal fishery.
g) Levels of domestic consumption, trends and trade.
No domestic consumption.
144
NATIONAL REPORT: ECUADOR
M. Verónica Toral-Granda1, Manfred Altamirano1 & Mario Piu2
1
Charles Darwin Foundation, Ecuador & 2Galápagos National Park Service, Galápagos Is., Ecuador
1. Information on wild populations
a) Species of non-commercial and commercial sea cucumbers in your country's waters: There are 38
species of sea cucumbers in the Galápagos islands (Maluf 1991) out of which only one species
Isostichopus fuscus is commercially harvested. In mainland Ecuador the populations are overexploited
and the only viable populations are found in the Galapagos Marine Reserve (GMR).
b) Area of distribution, and habitats if known: I. fuscus can be found in the eastern Pacific, from Baja
California, México to Ecuador, including Cocos Island (Costa Rica), Socorro Island (México) and the
Galápagos Islands (Ecuador) (Deichman 1958, Maluf 1991). In the Galápagos islands I. fuscus can be
found in all islands in rocky bottoms down to 39 m depth (Maluf 1991).
c) Abundance (including anecdotal information): Please refer to Martínez & Toral (2004).
2. Nature of sea cucumber fisheries
a) Commercial, artisanal, subsistence: There is an artisanal fishery with all catches for commercial exportation
to oriental markets.
b) Estimated number of fishers: 845 fishers and 313 fishing vessels were active in the 2003 season (Murillo
et al. 2003).
c) Type of fishing methods and gear equipment used: Hookah diving and hand collecting. All animals collected
are placed in a diving bag where kept until brought to the surface.
d) Licensing/permitting requirements: Any fishing activity within the Galápagos Marine Reserve (GMR)
must be done by a fishermen with a PARMA fishing license. No other specific licence or permit required
to partipate in a sea cucumber fishing season.
e) Sea cucumber farming, if any. None in the Galápagos islands, however studies are being undertaken in
mainland Ecuador to use abandoned shrimp farms to start rearing I. fuscus.
f)
Preferred markets (live vs. dried): Dried in the final destination; however, the produce leaves Galápagos
in brine.
g) Identification of the most important uses of sea cucumbers.
h) Landing data (species, bycatch, kg, sizes, etc), if available: Only I. fuscus is commercially harvested in
the Galápagos islands. No bycatch species have been recognised.
i)
Conservation measures (minimum harvesting size, closed areas, closed seasons, etc).
145
Table 1. Percentage of catches per fishing macrozone of I. fuscus in the fishing
seasons since 1999 until 2003 (Murillo et al. 2003).
Fishing macrozone
Isabela Oeste
1999
2000
37.3
2001
52.9
2002
2003
64.9
65.0
61.0
23.4
9.1
14.7
Fernandina
3.9
Santa Cruz
10.8
14.5
3.3
Isabela Sur
2.2
2.4
2.7
26.4
12.6
2.0
Isabela Norte y Este
6.4
7.6
2.0
18.7
Floreana
1.8
4.8
1.8
2.8
Española
11.1
5.2
0.0
1.0
TOTAL (%)
100
100
100
100
San Cristóbal
6.8
3.4
9.7
2.4
5.4
100
Total number of
individuals harvested 4 401 657 4 946 947 2 672 345 8 301 449 5 005 574
Average landing size
(live) (cm)
25.2
22.2
146
22.8
22.4
20.9
Table 3. Technical criteria used for the management of the sea cucumber
(Isostichopus fuscus) fishery in the Galápagos Marine Reserve since 1999
(Altamirano et al. 2004).
Technical Criteria
Fishing Season
1999
2000
2001
2002
2003
Two-Month season
1
1
1
1
1
Total Allowable Catch
(TAC)
1
1
1
−
1
Individual TAC
−
−
1
−
−
Fisheries Monitoring
1
1
1
1
1
Minimum Landing Size
−
−
1
1
1
2001
2002
2003
1
1
1
1
1
1
2001
2002
2003
Technical Criteria
Coastal Zoning
Closure of nursery
grounds
Technical Criteria
Closure of islands
Population density
evaluation
Catch Per Unit of Effort
(CPUE)
TOTAL
Fishing Season
1999
2000
−
−
−
−
Fishing Season
1999
2000
−
−
−
1
1
1
1
1
1
1
−
−
−
−
1
4
4
8
7
9
147
3. Domestic and International Trade: From Altamirano et al. 2004
a) Information on value, retail, wholesale prices and trends: To date, sea cucumber fishery is the most
lucrative fishing activity in the GMR (Murillo et al. 2003). From 1999 to 2003, a total of 25 327 972 sea
cucumbers were harvested. This equals 6856.41 tonnes fresh weight whole. After processing, this species
losses approximately 90% of its weight, giving approximately 671.2 tonnes dry weight.
This fishing activity has yielded a gross income of US$14 436 589 to the local artisanal fishing sector.
The market price per kg of individuals in brine in Galápagos was US$ 22.88 in 1999, $US 24.1 in 2000,
US$ 12.32 in 2001, US$ 14.96 in 2002 and US$ 22.88 in 2003 (Murillo et al. 2003).
According to Ecuadorian Export Statistics, Taiwan is the most important importer (73% of the total),
followed by USA and Hong Kong.
b) Export volumes, values and trends; import volumes, values and trends. N/A import data.
c) Information on key sea cucumber trading countries and territories.
d) Trade controls and enforcement, including identification of specimens in trade. The calcareous ossicles
(spicules) (taxonomic character for ID) remain untouched through the processing stages, thus validating
the use of this tool for identifying this species in the major importing countries.
e) Information on illegal, unreported and unregulated trade: Illegal fishing activities take place all year round
in the GMR, despite great effort from the Galapagos National Park Service. Most of the illegal catches
are shipped to mainland Ecuador, where it is transported by land to Peru where it is exported to Hong
Kong and other oriental markets.
f)
Levels of domestic consumption, trends and trade: No domestic consumption in Ecuador.
148
NATIONAL REPORT – FIJI
Mr Stanley A. Qalovaki
Department of Fisheries, Research Division, FIJI
1. Background
The harvesting, processing and export of sea cucumbers dates back to 1882, which was the beginning of
commercial exploitation of marine resources in Fiji waters. Since then, this fishery has fluctuated from very
extreme to almost non-existent. Lately, the sea cucumber fisheries have seen an increase in exploitation due to
various contributing factors, which are discussed below.
2. Information on wild populations
Table 1: A list of the commercial species of sea cucumbers in Fiji waters. Note: in the family
column, H = Holothuridae, S = Stichopodidae.
Common name
White teatfish
Black teatfish
Prickly redfish
Sandfish
Sandfish
Deepwater redfish
Stonefish
Surf redfish
Blackfish
Greenfish
Lollyfish
Elephant trunkfish
Curryfish
Amberfish
Brown sandfish
Tigerfish
Leopard fish
Pinkfish
Scientific name
Microthele fuscogilva
M. versicolor
Thelenota ananas
Holothuria scabra
H. versicolor
Actinopyga echinitus
A. lecanora
A. Mauritania
A. miliaris
Stichopus cholonotus
Holothuria atra
H. fuscopunctata
Stichopus variegatus
Thelenota anax
Bohadshia marmorata
B. argus
B. anaes
Holothuria edulis
Family
H
H
S
H
H
H
H
H
H
S
H
H
S
S
H
H
H
H
Value
High
High
High
Med/high
Med/high
Med
Med
Med
Med
Med
Low
Low
Low
Low
Low
Low
Low
Low
Two non-commercial species in the wild are:
i)
ii)
Bohadschia geoffreyi (Holothuridae)
B. graeffei (Holothuridae)
These sea cucumbers are distributed throughout all the inshore coastal waters of the islands of Fiji, their
habitats ranging from shallow sea grass beds and sandy bottoms (sandfish), deep lagoons ( Blackfish), reef
flats (leopardfish), backreef slopes (surf redfish) to very deep parts of the backreef (white teatfish).
149
However, the abundance of individual species vary greatly from one coastal water to another, due to the
following factors:
a) Environmental factors – which might favour one species over another;
b) Traditional beliefs – some tribes have certain species of sea cucumbers as their totem thus
protect it more than others;
c) Religious practice – some religions ban the consumption of sea cucumbers and in some cases
in Fiji a whole clan (which could be one 3-4 villages) along the coast might observe this ritual;
d) Degree of isolation – if the reefs are very far from the main urban centres, than it won’t be
under high fishing pressure; and
e) Habitat destruction.
3. Nature of sea cucumber fisheries
Commercial harvesting is the greatest threat to this marine resource, and has a huge impact on artisanal and
subsistence fisheries as well. Licensed companies not only buy from artisanal fishers, but also send out diving
teams (15-30 divers/team) who use UBA to gather for sea cucumbers from deeper waters. The use of SCUBA
(both scuba or hookah) is illegal for any fishing activity unless approved by “special exemption” of the minister
concerned, and most diving teams have had their request denied but use UBA anyway. All stakeholders
(Fisheries Dept, Police and local communities) work together in trying to eradicate this illegal activity.
Artisanal and subsistence fisheries almost always occur together but at present, it is becoming more frequent
because of the presence of ‘commercial traders’ or agents of licensed companies. These agents are located at
strategic positions amongst the coastal villages, even on isolated island that have only 2-3 villages. This factor
has really accelerated the gleaning rate of sea cucumbers, and especially when the companies are willing to buy
it live because it is cheaper for them, while the fishers favour it because it involves less work, no risks and quick
cash.
Any Fijian can indulge in artisanal and subsistence a fishery of sea cucumbers without a licence, provided it is
done within their customary fishing grounds, so practically everyone gleans. From the list of companies in table
2, one can deduce the number of agents they have and how many fishers are out there for them
Table 2: List of approved BDM exporters as of 10/02/04.
COMPANY
OPERATION STATUS
1. Gold Hold Co. Ltd
Active
2. Kung Wah Trading Co. Ltd
Active
3. Star Dragon General Trading Co.
Active
4. Golden Dove Investment Ltd
Active
5. C&J Enterprise
Active
6. Tuvu seafood (Fiji) Ltd
Active
There are 7 more approved companies who are under the ‘yet to operate’ status, so when they are active, the
total number of companies would be 13.
150
The main fishing methods for sea cucumbers are:
a) Gleaning – occurs during low tide
b) Free dive – occurs in deeper waters during low and high tides
c) Bomb – a spear head partly embedded in concrete is dropped on target species at location too
far down for diver to free dive
d) SCUBA – scuba or hooker is used to access depths where free diving is impossible for prolonged
periods. This is illegal but is becoming more frequently employed by divers.
At present there is no sea cucumber farming by any private entrepreneur, but it is part of the Fisheries
Department’s ongoing trial at it’s Makogai Research Station.
Apart from it’s economic value, only 2 species (Holothuria scabra & H. versicolor) are frequently used as
food.
4. Management and conservation
Government is concerned about the current status of the sea cucumber fisheries, thus it has taken the following
steps:
a) Working in collaboration with NGOs, research institutions and concerned communities in over
fished areas to set up management plans where such tools as ‘Closed Areas’, or ‘reduction of
licence issued’ are employed
b) The formation of a BDM council by all companies concerned with Fisheries Department. The
council is working on a set of guidelines that will protect the industry and ensure the sustainability
of the sea cucumber fisheries
c) In 1984, Government approved the ‘BDM exploitation guidelines’ that clearly states who
should harvest and process BDM, which species are banned from exporting, the size limitations
for harvesting (3 inches), and which gears are banned for sea cucumber harvesting. Most of
these regulations need education / awareness campaigns and tighter enforcement of the law
but for size limitation, government is looking into the ‘one size fits all’ issue which are continually
being raised by researcher and industry members.
However, one of the major hindrance to the effectiveness of the Fisheries Department’s role in regards to the
policing, enforcement and research of sea cucumber issues is funding.
5. Domestic and international trade
Out of all the sea cucumbers species in Fiji, only 18 are of commercial importance. Sea cucumbers processed
into BDM products are traded internationally to Asian and American markets. An increase in market demand
has led to the harvesting and processing of more quantities of low value species, irrespective of size limitations.
The export markets have now extended to the European countries of Italy and Spain, Asian markets of Hong
Kong, China, Korea, Singapore and Taiwan, American markets in the USA and Canada.
151
The commercial exploitation of sea cucumbers began in the 18th century; however, export volumes recorded
over the last century revealed that BDM had never exceeded 50 tonnes per annum. Yet, the industry have
expanded and diversified into isolated areas in the last 20 years due to improved transportation infrastructure,
and harvesting effort has intensified to meet the market demand. This has led to an increase in fishing pressure
at new fishing grounds and isolated reefs, increase in number of fishers and extensive use of UBA’s.
Unfortunately, the production volume still remains low despite an increase in fishing effort. The production of
800,000 Kg with a value of $15m peaked in the early 1990’s; however, it continually declined after that (refer
table 3).
Table 3: Export weight and value of BDM
YEAR
Early 1990
1998
1999
2000
2001
WEIGHT (Kg)
800,000.00
369,261.50
140,695.00
246,001.50
244,971.00
VALUE (FJD$)
15,000,000.00
9,785,918.00
3,585,618.00
6,659,532.00
6,468,610.50
The data clearly indicates that the resource is under pressure, and if no proactive measures are enforced, than
there will be a catastrophic effect on the - industry, economy, recovery period for the resource in the wild,
inshore coastal marine ecosystem, employment opportunity and readily available food source in disastrous
times.
152
NATIONAL REPORT – INDONESIA
Asep Sugiharta
Directorate of Biodiversity Conservation, Ministry of Forestry INDONESIA
1. Introduction
Sea cucumbers or holothurians are sausage-shaped marine animals commonly observed on sand bottoms.
They are harvested for food such as a base for soups in Asia (Allen, 1996). Sea cucumber known as teripang
is one of alternative-valuable marine resources for local fishermen in Indonesia. Habitat distributions of sea
cucumbers are widespread over the country, perhaps potentially in middle to eastern parts such as Sulawesi
and Maluku. Practices of sea cucumber harvest have been running for years especially in a difficult season
during extreme west and east monsoon. Sea cucumber is relatively easy to be collected by local inhabitants
because its habitat is in shallow seashore water generally adjacent to villages. Collected sea cucumbers are
sun dried for a few days before being sold to traders.
2. Conservation and trade
Harvesting on sea cucumbers by local people is under authority of the Ministry of Marine and Fishery, and
regulated under the Act of Fishery (number 9, year 1985). There is lack of information concerning a number of
sea cucumbers in trade as sea cucumbers are a non-target commodity of marine resources. The large number
of fisheries still concentrate in their activities to catch fishes which is abundance over the country, besides the
domestic market are not familiar to consume sea cucumbers. Neglecting to understand the biology of the
species within high market demand would be endangered of the species in the near future. The cultivation of
sea cucumbers that has been initiated is focused to fulfill a potential overseas-market, especially to the countries
such as Hongkong and Taiwan (personal communication with a staff of the Ministry of Marine and Fishery).
Action to be designed in Year 2004-2005
•
Setting a management and conservation of sea cucumbers for short, middle, and long terms.
•
Identifying habitat distribution and status population of sea cucumbers in selected locations.
•
Recording sea cucumbers in trade in selected landing ports.
References
Allen, Gerald. 1996. Marine Life of Indonesia and Southeast Asia. Periplus Editions. Singapore.
153
NATIONAL REPORT – JAMAICA, WEST INDIES
Karl A. Aiken, PhD
Department of Life Sciences, University of the West Indies, Mona Campus, Kingston, Jamaica
1. Information on wild populations
a) Species
The species of the Class Holothuroidea, families Holothuroidae and Stichiopidae thought to be occurring in
Jamaican waters include the following. Table 1 also provides an assessment of potential commercial use
based mainly on size.
Table 1. Species of sea cucumbers known from Jamaican and adjacent waters with
assessment of potential commercial importance (Adapted from Humann, 1992; Kaplan,
1982 ; Colin, 1978).
Scientific name
Common name
Astichopus
Furry sea cucumber
multifidus
Actinopygia agassizii Five-Toothed Sea
Cucumber
Isostichopus
Three-rowed sea
badionotus
cucumber
Eostichopus amesoni Conical Sea
Cucumber
Holothuria mexicana Donkey Dung Sea
Cucumber
Holothuria
Surinam sea
surinamensis
cucumber
Holothuria arenicola Burrowing sea
cucumber
Holothuria impatiens Slender Sea
Cucumber
Holothuria thomasi
Tiger Tail Sea
Cucumber
Holothuria
Brown rock sea
glaberrima
cucumber
Holothuria grisea
Grey sea cucumber
Holothuria floridana Florida sea cucumber
Euapta lappa
Beaded sea cucumber
Holothuria parvula
Golden sea cucumber
Pentacta pygmea
Pygmy sea cucumber
154
Potential
commercial use
(size range or
max. size, cm)
* (to 45 cm) but
deep (see Table 2)
* 20 – 30 cm)
Noncommercial
species
*(20 – 45 cm)
*(20 – 40 cm)
* (25 - 40 cm)
* (to 20 cm)
*(10 - 25 cm)
* (20 – 30 cm)
*(90 – 180 cm)
*(10 -15 cm)
*(to 20 cm)
*(to 20 cm)
* (22 - 90 cm)
*(3.5 cm)
*(to 10 cm)
b) Area of distribution, habitats & abundance
Preliminary data of the species listed in Table 1 is summarized in Table 2 below.
Table 2. Distribution, habitat preferences and abundance of species of sea cucumbers from
Jamaica (adapted from Humann, 1992; Kaplan, 1982; Colin, 1978).
SPECIES
DISTRIBUTION
HABITAT
Astichopus
multifidus
Actinopygia
agassizii
Isostichopus
badionotus
Florida, Bahamas,
Caribbean, Jamaica
Florida, Bahamas,
Caribbean, Jamaica.
Florida, Bahamas,
Caribbean incl. Jamaica.
Eostichopus
amesoni
Holothuria
mexicana
Holothuria
surinamensis
Caribbean incl. Jamaica.
Deep sandy areas around
reefs.
Sea grass beds and sandy
around reefs.
Sea grass beds, shallow
reef rubble patches, sandy
areas around reefs.
Reef rubble patches and
sandy areas around reefs.
Sea grass beds and sandy
areas around reefs.
Among algal tufts, among
finger-coral colonies
Holothuria
arenicola
Holothuria
impatiens
Holothuria thomasi
Holothuria
glaberrima
Holothuria grisea
Holothuria
floridana
Euapta lappa
Holothuria parvula
Pentacta pygmea
Caribbean incl. Jamaica;
Bahamas, not in Florida.
Bermuda, Florida
Jamaica, Antigua.
Bermuda to Brazil (incl.
Jamaica)
Florida, Bahamas,
Caribbean incl. Jamaica,
also circumtropical.
Florida, Bahamas,
Caribbean incl. Jamaica.
Caribbean incl. Jamaica,
not in Florida
Caribbean incl. Jamaica,
Florida, not in Bermuda
Coral debris, sand flats
Under rocks, crevices in
reefs, reef rubble and in
open water.
Lagoons, protected water
with rubble bottoms.
On & under rocks in surf
zone
Young among rock or
coral debris, adults in
Turtle grass
Florida, Jamaica, western Near mangrove swamps,
Caribbean, Dutch
turtle grass beds
Antilles
South Florida, Bahamas, Hide under coral slabs,
Caribbean incl. Jamaica
rubble and in recesses
during the day.
Bermuda , Caribbean,
Under rocks in reef flat,
(Jamaica?
shallow water and tide
pools
Florida Gulf Coast,
Shallow rocky bottoms,
Puerto Rico, Trinidad,
turtle grass beds
Brazil, (Jamaica)?
155
ABUNDANCE
IN JAMAICA
Occasional but
deep
Occasional
Common
Uncommon
Common
Common
Occasional
Uncommon
Occasional
Occasional
Common
Common
Occasional
Unknown
Unknown
Abundance notes
Generally, little is known of the relative abundance of the species of sea cucumbers in Jamaica’s waters. What
little exists is summarized in the preceding tables and is based on identification texts and personal observations
during 30 years of diving and marine field trips and research in coastal waters.
Certain species may have apparently changed in their abundance. For example, the large species Holothuria
mexicana, donkey dung sea cucumber, between 1980 and 1988 was relatively abundant around the University
of the West Indies Discovery Bay Marine Laboratory precincts, which is located almost exactly in the middle
of the north coastline. They were readily observed in the shallows around the lab and near the adjoining back
reef lagoon. For the last few years their number is relatively few. What factor(s) might have brought about this
apparent significant decline in abundance is unknown. It must, however, be mentioned that there were two
major hurricanes (tropical cyclones) in 1980 and the other in 1988 which seriously impacted the reefs in the
area. Combined with coral diseases, sea urchin die-offs and sea surface temperature increases over the same
time, one or more or all of these factors may be related to or responsible for this change.
2. Nature of sea cumber fisheries
a) Sea cucumbers are not consumed in Jamaica and historically never were consumed by the population.
Thus, there is no traditional fishery for or interest of any kind in them. There are a very few anecdotal
stories of Japanese embassy staff asking for marine biology students to deliver any sea cucumbers
collected to them for consumption in the late 1980’s (M. Jones-Williams, pers. comm.. 2004).
b) Estimated number of fishers: None
c) Type of fishing methods and gear: None
d) Licensing/permitting: None
e) Sea cucumber farming: None
f) Preferred market(s): None, although in 1991 a small team of Chinese businessmen asked a local
fishing business to organise an assessment of the sea cucumber stock in local waters. This was done,
but the results are unknown. Importantly, no directed fishery for sea cucumbers was known to have
developed after this survey.
g) Identification of most important uses of sea cucumbers: No sea cucumber species is caught or
consumed.
h) Landing data: None are landed.
i)
Conservation measures: As no sea cucumbers are landed, none is in place. If a market were to develop,
the species would be protected under the new Fisheries Bill which is shortly to be introduced. This Bill
replaces the older Fishing Industry Act of 1976. They would also be included under parts of the
Wildlife Protection Act which is administered by the National Environmental Planning Agency (NEPA).
156
3. Domestic and international trade
There is no landing of seas cucumbers in Jamaica, so there is no trade. The only known interest from outside
Jamaica in possibly exporting Jamaican sea cucumbers, took place in 1991. Though a small survey was done,
nothing apparently came of this effort by a Chinese business enterprise.
4. Summary
It would appear that there is a great lack of detailed relevant, basic biological and ecological information on the
members of the Order Holothuroidea in Jamaican waters. Even information on the identification of the species
that actually occur in Jamaica is uncertain and poor at the time of writing. Data included in this present paper
would represent the first known compilation. Therefore, there is considerable need for the investigation into
these biological aspects, and an assessment of the status of the several species occurring, prior to any
conservation measures that may be suggested and/or introduced. Any potential decisions on international
trade enquiries must be based on sound recent scientific data on local species of sea cucumbers, of which there
is almost none at present. The University of the West Indies, Life Sciences Department, Mona campus, is thus
presently seeking funding a proposal for baseline biological research into Jamaican sea cucumber species.
Such research when completed, could form the basis of preliminary conservation and management regulations
for the species should they be necessary.
REFERENCES
Colin, P.L. 1978. Caribbean reef invertebrates and plants, a field guide to the invertebrates and plants
occurring on coral reefs of the Caribbean, the Bahamas & Florida. T.F.H. Publications, New Jersey,
USA
Humann, P. (Loach, N. ed.) 1992. Reef creature identification, Florida, Caribbean, Bahamas. New World
Publications, Inc. Florida
Kaplan, E.H. 1982. A field guide to coral reefs of the Caribbean and Florida including Bermuda and the
Bahamas. Petersen Field Guide Series. Houghton Mifflin Company, Boston.
157
NATIONAL REPORT – JAPAN
Shingo Fukui
Fisheries Agency, Government of Japan
INTRODUCTION
More than 100 species of sea cucumbers are found in Japan. Among sea cucumbers belonging to the families
Holothuridae and Stichopodidae, the species mainly harvested and used commercially is Apostichopus japonicus.
Historically, descriptions on the use of sea cucumbers in Japan are found in the writings of early 8th century.
Further, since the end of the 17th century, dried sea cucumber, called "iriko", had been exported to China (then
Qing dynasty), constituting Japan's major export item. At present, most of Apostichopus japonicus harvested in
Japan are distributed in the domestic market. It is eaten raw with soy sauce and vinegar, and salted fermented
products (shiokara) of digestive organs called "konowata" and dried gonad called "konoko" are cherished as
delicacies and high-grade food materials.
In sea cucumber fishery in Japan, diverse resource management measures adapted to the regional situation are
taken, such as regulations on fishing gear, fishing methods, fishing season and size limitation as well as larvae
release. Thus sea cucumbers are used in a sustainable way. Further, as the bulk of the harvest is used for domestic
consumption, it is considered that international trade in this species has little or no impact on the population.
Therefore, management under the Convention for Trade in Endangered Species of Wild Fauna and Flora (CITES)
is not an appropriate approach.
In order to discuss conservation and management regarding sea cucumbers, it should be emphasized that each
country and the United Nations Food and Agriculture Organization (FAO) need to collect and collate on a
preliminary basis the basic data such as the state of the sea cucumber resources, situation of the catch, and actual
state of utilization. If each country and FAO implement fisheries management based on such basic data, it will be
possible to ensure sustainable utilization of sea cucumbers in the world. Japan expects that its experience in the
management of sea cucumber fisheries will contribute to the realization of sustainable utilization of sea cucumbers
in the world.
1. Information on wild populations
a) Species of non-commercial and commercial sea cucumbers in your country´s waters
In Japan, many species of temperate and tropical sea cucumbers are found. Subjected to harvesting among them
are Apostichopus japonicus, Thelenota ananas, Stichopus chloronotus belonging to Stichopidea family, and
Holothuria (Halodeima) arta, H.scabra belonging to Holothuriidae family. The species harvested for commercial
purpose is mostly Apostichopus japonicus. The list of sea cucumber found in Japan is shown in Attachment 1.
2. Nature of sea cucumber fisheries
a) Commercial, artisanal, subsistence.
Most of the fisheries targeting sea cucumbers are commercial operation targeting temperate-zone Apostichopus
japonicus, and the catch is distributed as live products in the domestic market. In some part of Okinawa, artisanal
fisheries targeting tropical sea cucumbers are practiced.
158
b) Estimated number of fishers
The number of people engaged in coastal fisheries in Japan is about 215,000. In many cases, sea cucumber
fisheries are conducted seasonally by coastal fishermen, and the number of fishing enterprises engaging in sea
cucumber fisheries is estimated to be at least over 10,000. Therefore the number of fishers engaging in this fishery
is estimated at several tens of thousand.
c) Type of fishing methods and gear equipment used
Sea cucumbers are harvested mainly by trawling using small-size engine-powered fishing vessels (sea cucumber
dredge net fisheries) and fisheries using diving equipment. It is also harvested by diving, spear and ring nets.
d) Licensing/permitting requirements
In order to promote protection of breeding habitat and rational utilization of sea cucumbers, the Japanese government
is adopting fishery license and fishery right systems, as in the following, based on fisheries-related laws. Any
person engaging in violation relating to the fisheries license and fishery rights is subjected, as juridical penalties, to
imprisonment and/or fines and other administrative proceedings.
Fisheries license: The government is placing the types of fisheries having high-level capability to harvest sea
cucumbers (e.g. bottom trawl fisheries) under the license system in all areas of Japan. Further, prefecture governors
are placing under the license system the fisheries capable of harvesting sea cucumbers exceeding certain quantities
(bottom trawl fisheries using small-size engine-powered fishing vessels (sea cucumber dredge net fisheries) and
fisheries using diving equipment).
Fishery right: Besides the fisheries license, the prefecture governors confer, based of the fisheries-related laws,
the responsibility to conserve resources to fishermen's groups utilizing and depending on sea cucumber resources
historically and socio-economically, by granting them the right to harvest sea cucumbers exclusively in certain
areas of sea. Prefecture governors implement protection of sea cucumber resources by establishing limitations
and conditions to the fishery right in case fishermen's groups do not take appropriate resource conservation
measures for sea cucumbers.
e) Sea cucumber farming, if any
No aquaculture of sea cucumbers is carried out, but farming of Apostichopus japonicus is widely practiced.
Full-scale development of artificial larvae production technology has been promoted since 1977, and in 2001, a
total of 1,877,000 artificial larvae were produced at 10 larvae production centers in Japan. Also, natural larvae
harvesting has been conducted to collect juvenile sea cucumbers attached to oyster shells, etc. in the natural sea
environment. The number of larvae released for both types of culture in 2001 was 3,648,000.
f) Preferred markets (live vs. dried)
g) Identification of the most important uses of sea cucumbers
At present, most of Apostichopus japonicus harvested in Japan are distributed as live products in the domestic
market, and are consumed raw with soy sauce and vinegar. Salted fermented products of digestive organs called
"konowata" and dried gonads called "konoko" are cherised as delicacies and high-grade food materials. Some
sea cucumbers are processed into dried products and are exported.
159
h) Landing data (species, bycatch, kg, sizes, etc), if available
The catch volume in 2001 was 7,229 tons, worth about 4.1 billion yen, all of them being Apostichopus japonicus.
Apostichopus japonicus is harvested by fisheries mainly targeting this species, and there is little or no bycatch by
other fisheries nor are there bycatches of other species of sea cucumbers.
i) Conservation measures (minimum harvesting size, closed areas, closed seasons, etc)
Regarding conservation and management of sea cucumber fisheries, sustainable utilization is ensured with detailed
region-to-region regulations, including obligatory and voluntary measures. Major conservation and management
measures include the establishment of closed seasons (protection during the spawning seasons), limitations on the
number of licensed fishing vessels, vessel tonnage, fishing gear, fishing seasons, fishing hours, fishing areas, size
and weight, and catch volume and value. As an example, a specific case of conservation and management measures
implemented in Hokkaido, the most producing prefecture, is presented in Attachment 2.
Further, in addition to management measures, improvement of fishing ground, which serve as resting habitat and
reproduction area of sea cucumber, by accumulating rocks and establishing reefs for sea cucumber in order to
ensure increase of the population.
3. Domestic and International Trade
a) Information on value, retail, wholesale prices and trends
The prices of fresh Apostichopus japonicus distributed in Japan differ from season to season. (Prices are highest
in the New Year season when demand is high.) The average wholesale price per kilogram is about 500 yen, with
retail prices standing at 1,500 yen to 5,000 yen. "Konowata"(salted fermented products of digestive organs),
which is a delicacy fetches 2,500 yen per 80g container, and "konoko" (dried gonad) is about 4,000 yen per 20g.
b) Export volumes, values and trends; import volumes, values and trends
The only sea cucumber product being exported is dried sea cucumber, and a small amount of frozen and salted
dried products are imported.
Exports: There is no export statistic item of dried sea cucumber in Japan, and the products are included in the
category of "Other mollusk and aquatic non-vertebrate animals." Exports in 2002 were about 90 tons, with
export value of about 1.7 billion yen, of which a substantial part is taken by dried sea cucumbers.
Imports: A total of 270kg of frozen products worth 800,000 yen, and 1.2 tons of salted dried products worth 4
million yen were imported in the same year.
c) Information on key sea cucumber trading countries and territories
Dried sea cucumbers from Japan are being exported to China, Hong Kong, and Taiwan.
d) Trade controls and enforcement, including identification of specimens in trade
160
Effective from January 2004, "dried sea cucumber" was added to Japan's export statistic item, and exports
volume came to be accurately grasped by the customs office. However, accurate species-to-species identification
is not possible even by experts. Unless species-to-species trade enforcement method is established, it would not
be possible to control trade properly.
e) Information on illegal, unreported and unregulated trade: None
f) Levels of domestic consumption, trends and trade
At present, a dominant portion of Apostichopus japonicus harvested in Japan are distributed in Japan as
live products, and consumed raw with soy sauce and vinegar. Salted fermented products of digestive tube called
"konowata" and dried gonads called "konoko" are cherished as delicacies and high-grade food materials
Sea cucumbers belonging to the families Stichopodidae and Holothuriidae found in Japan
Family Stichopodidae
Apostichopus japonicus (Liao, 1980):
Commonly sighted in various parts of Japan (from Hokkaido to Kyushu). Found in the boulder stone zone in
the shallow sea area. It is an important edible species. "Iriko"(dried sea cucumber) is used in the Chinese
cuisine, and salted fermented products of internal organs is cherished as "konowata".
Thelenota anax (H.L.Clark, 1912):
Distributed in Japan (shallow sea south of Okinawa), Madagascar, Australia, New Caledonia, Guam, and
China.
Parastichopus nigripunctatus (Augstin, 1908):
Japan (found at the sea depth of 20-600m from Hokkaido to Kyushu)
P. multidentis (Imaoka, 1991):
Japan (East China Sea (136m), off Koshiki island (330-380m))
Thelenota ananas (Jager, 1833):
Japan (found on the coral sand filter in the shallow sea of south of the main Okinawa Island), Australia, Fiji,
New Caledonia, Indonesia, Guam, China, and Taiwan. Dried products of this species are called "gajimaru" in
Okinawa, and "bai-ka-san" in China. They are both high-graded products.
Stichopus chloronotus (Brandt, 1835):
Japan (found in the reef zone in the shallow sea south of the Amami Oshima Islands). Distributed extensively
from the Indian Ocean to western Pacific (New Caledonia, Australia, Guam, the Philippines, Hawaii, and
China).
Stichopus ohshimae (Mitsukuri, 1912):
Japan (found in reef zone of the shallow sea south of Izu Peninsula).
Stichopus horrens (Selenka, 1867):
Japan (Kakeroma Island in the Amami Oshima Islands), Maldive, Australia, New Caledonia, New Guinnea,
the Philippines, Guam, Hawaii, China, and Taiwan.
Stichopus pseudhorrens (Cherbonnier, 1967):
Japan (Kurosaki in Amami Oshima Islands, Okinawa), and New Caledonia.
Stichopus hermanni (Semper, 1868):
Japan (found in the sandy area of the reef area, south of Okinawa), Australia, the Philippines, and Sumatra.
Stichopus variegatus (Semper, 1868):
Japan (Okinawa), Red Sea, Australia, New Caledonia, Indonesia, the Philippines, Palau, China, and Taiwan.
161
Sea cucumbers belonging to the families Stichopodidae and Holothuriidae found in Japan
Family Holothuriidae
Actinopyga lecanora (Jager, 1833):
Southeastern Asia south of Japan (Okinawa, Ogasawara Islands), South Pacific.
A. miliaris (Quoy et Gaimard, 1833):
Japan (south of Amami Oshima Islands, Ogasawara Islands)
Bohadschina marmorata (Jager, 1833):
Southeast Asia south of Japan (coral reefs in the shallow sea south of Okinawa), and South Pacific.
Holothuria (Platyperona) macteari (Bell, 1884):
Southeastern Asia south of Japan (Okinawa, Ogasawara Islands), and South Pacific
H. (Lessonothuria) isuga (Mitsukuri, 1912):
Southeast Asia south of Japan (Chinenzaki on the main Okinawa Island), and South Pacific.
Actinopyga mauritiana (Quoy et Gaimard, 1833):
Japan (Ogasawara Islands, reef zone south of Amami Oshima Islands), Fiji, New Caledonia, Samoa, Tahiti,
Australia, Guam, China, and Taiwan.
Actinopyga echinites (Jager, 1833):
Japan (found in sand filter zone at the sea depth of 0-30m in Okinawa), Sri Lanka, Celebes, Fiji, Australia,
New Caledonia, China, and Taiwan.
Actinopyga sp.:
Japan (Kahi Island and Kuroshima Island in the Okinawa Islands; found in the coral sand filter zone in the
shallow sea).
Bohadschia graeffei (Semper, 1876):
Japan (found in the sand filter and reef zones at the sea depth of 5-20m in southern Okinawa), Red Sea,
Maldive, Australia, New Caledonia, Indonesia, the Philippines, Guam, Papua New Guinnea, China, and
Taiwan.
Bohadschia vitiensis (Semper, 1867):
Japan (found in the sandy zone of shallow sea south of Amami Oshima Islands), New Caledonia, Fiji, Samoa,
and Java.
Bohadschia bivittata (Mitsukuri, 1912):
Japan (found in the shallow sea of Okinawa)
Bohadschia argus (Jager, 1833)
Japan (found in the shallow sea of Amami Oshima Islands), Sri Lanka, Timor, Celebes, Fiji, Samoa, Tahiti, the
Philippines, New Caledonia, Guam, Indonesia, Malaysia, Australia, China, and Taiwan.
Bohadschia sp.:
Japan (found in the coral sand filter zone in Kuroshima in Okinawa Islands).
Holothuria (Selenkothuria) moebii (Ludwig, 1883):
Japan (found in the sand filter on the beaches from Boso Peninsula to Okinawa), China, and Taiwan.
Holothuria (Semperothuria) cinerascens (Brandt, 1835):
Japan (southern Kii Peninsula, Makurazaki, Okinawa, Ogasawara Islands. Found in the dent of rocks near
low-tide zone).
H. (Halodeima) edulis (Lesson, 1830):
Japan (found in the shallow sea south of Amami Oshima Islands), Red Sea, Sri Lanka, Timor, New Caledonia,
Guam, Celebes, Fiji, Tahiti, Hawaii, and China.
H. (Platyperona) difficilis (Semper, 1868):
Japan (Kushimoto, Amami Oshima Islands, Ogasawara Islands. Small individuals are found in the tide pools
and under rolling rocks in the low-tide area while large individuals are found in the boulder stone zone at the
sea depth of several meters), Samoa, Australia, Guam, China, and Taiwan.
162
Sea cucumbers belonging to the families Stichopodidae and Holothuriidae found in Japan
H. (Thymiosycia) hilla (Lesson, 1830):
Japan (found in reef zone in Okinawa Islands), Red Sea, Australia, New Caledonia, Guam, Hawaii, Panama,
China, and Taiwan
H. (Thymiosycia) arenicola (Semper, 1868):
Japan (coral sand filter zones in Okinawa Islands), Australia, Guam, the Philippines, China, and Taiwan.
H. (Thymiosycia) impatiens (Forskal, 1775):
Japan (Kuroshima in the Okinawa Islands. Found from reef to sand filter zones in the shallow sea.), the
Mediterranean Sea, Red Sea, Sri Lanka, Timor, the Philippines, Australia, Samoa, Tonga, Tahiti, New
Caledonia, Guam, Hawaii, Panama, Florida, China, and Taiwan
Holothuria (Thymiosycia) decorata (von Marenzeller, 1882):
Japan (Miura Misaki, Kominato, Shirahama, Awaji Island, Iki Island, Bungo, Kochi. Found at the sea depth
of 0-200m. In the shallow water, found in the sand filter zone). Host to pearl fish.
H. (Halodeima) arta (Jager, 1833):
Japan (found reef zone south of Tokara Archipelago), Red Sea, Sri Lanka, Timor, New Caledonia, Guam,
Celebes, the Philippines, Australia, Tonga, Tahiti, Samoa, Hawaii, Florida, Jamaica, China, and Taiwan.
Large individuals of over 50cm are found in the tropical region. "Iriko" is produced.
H. (Mertensiothuria) leucospirota (Brandt, 1835):
Japan (south of Izu Peninsula; reef zone of the shallow sea), Sri Lanka, Australia, Fiji, the Philippines, Samoa,
Tahiti, New Caledonia, Guam, Hawaii, China, and Taiwan. Poisonous with Cuvierian tubles.
H. (Mertensiothuria) pervicax (Selenka, 1967):
Japan (south of Miura Peninsula; found in the reef and boulder stone zones in the shallow sea), Red Sea, the
Philippines, Australia, Samoa, New Caledonia, Guam, China, and Taiwan
H. (Mertensiothuria) fuscocinera (Jager, 1833):
Japan (Kuroshima of the Okinawa Islands; found in the sandy zone of coral reef or in sand filters), New
Caledonia, Australia, China, and Taiwan
H. (Mertensiothuria) sp.:
Japan (Taira Bay of the main Okinawa Island; found in the sand of reef)
H. (Lessonothuria) pardalis (Selenka, 1867) :
Japan (South of Izu Peninsula; somewhat buried in the sand filter under the boulder stones around low-tide
zone, or found among boulder stones), Red Sea, Sri Lanka, Samoa, Australia, the Philippines, New Caledonia,
Guam, Hawaii, China, and Taiwan
H. (Metriatyla) scabra (Jager, 1833)Japan (south of Amami Oshima Islands; found in coral sand in the shallow
sea), India, Solomon Islands, Indonesia, Red Sea, Sri Lanka, Singapore, Celebes, the Philippines, Fiji, New
Caledonia, and China.
H. (Microthele) nobilis (Selenka, 1867) : Distributed in Japan (found in the coral sand filter in the shallow sea
of Okinawa Islands), New Caledonia, Australia, Guam, China, and Taiwan.
163
Management measures for sea cucumber fishery in Hokkaido
Contents of regulations
Regulations, etc.
Hokkaido marine fisheries
# License system for fisheries
- trawl fishery using small-type engine-powered boats (sea adjustment regulation
Article 5
cucumber dredge net)
*All require approval for
- Diving fishery
implementation based
on fishery right
# Establishment of closed season (protection of spawning season)
Hokkaido marine fishery
- May 1-June 15--Offshore area of Ishikari, Shiribeshi, Abashiri, adjustment regulation
Soya and Rumoi Districts
Article 39
- June 21-August 20--Offshore area of Hiyama, Watarijima and
Iburi Districts
- July11-September 20--Offshore area of Hidaka, Tokachi, Kushiro
and Nemuro Districts
(i) Limitation on the number of license and the number of operating Regulation on the exercise
vessels [entire Hokkaido]
of fishery right
(ii) Limitation on tonnage of fishing vessels used
- Hamamasu: less than 5 tons; Atsuta: less than 10 tons [Ishikari]
- Rausu: less than 5 tons; Notsuke, Betsuumi, mid part of Nemuro
Bay, Nemuro, Habomai, Ochiisi: less than 10 tons; Shibetsu: less
than 15 tons [Nemuro]
- Oumu: outboard motor; Monbetsu: spoon net: less than 3 tons;
Saruru, Monbetsu: diving equipment; Shari, Utoro: less than 5 tons;
Yuubetsu: less than 10 tons; Oumu, Saroma, Tokoro: less than 15
tons [Abashiri]
- Esashi: less than 7 tons [Soya]
Regulation on the exercise
of fishery right
voluntary regulation
Regulation on the exercise
of fishery right
(iii) Limitation on fishing gear used
# Limitation on fishing methods, etc.
- dredge net, Rausu diving equipment, Notsuke spoon net fishery
[Nemuro]
Regulation on the exercise
- dredge net, spoon net or diving equipment, gaff or diving of fishery right
equipment [Abashiri]
- dredge net: up to 2; Tomamai-Haboro: gaff 2-3; Yagishiri: spoon
net: up to 2 [Rumoi]
voluntary regulation
# Limitation on the scale of fishing gear
Regulation on the exercise
- Length of nets: up to 280cm [Ishikari]
of fishery right
- Sawara-Otoshibe: dredge net mesh size: 75mm or larger voluntary regulation
[Watarijima]
- dredge net mesh size: 45.45-75mm; dredge length: 3.18m-4m
[Abashiri]
(iv)Limitation on fishing season
- Yoichi: July 16-March 30; voluntary halt of operation [Shiribeshi]
- Esashi, Kaminokuni area: December, January: harvesting voluntary regulation
prohibited
Otobe area: November, December: harvesting prohibited
Taisei(Kaitorima) area: November 21-April 9: harvesting prohibited
Sedana area: January-March: harvesting prohibited [Hiyama]
- Operation season: Yakumo: November 1-March 31 [Watarijima]
voluntary regulation
164
(i) Limitation on the number of license and the number of operating Regulation on the exercise
of fishery right
vessels [entire Hokkaido]
(ii) Limitation on tonnage of fishing vessels used
- Hamamasu: less than 5 tons; Atsuta: less than 10 tons [Ishikari]
- Rausu: less than 5 tons; Notsuke, Betsuumi, mid part of Nemuro
Bay, Nemuro, Habomai, Ochiisi: less than 10 tons; Shibetsu: less
than 15 tons [Nemuro]
- Oumu: outboard motor; Monbetsu: spoon net: less than 3 tons;
Saruru, Monbetsu: diving equipment; Shari, Utoro: less than 5 tons;
Yuubetsu: less than 10 tons; Oumu, Saroma, Tokoro: less than 15
tons [Abashiri]
- Esashi: less than 7 tons [Soya]
Regulation on the exercise
of fishery right
voluntary regulation
Regulation on the exercise
of fishery right
(iii) Limitation on fishing gear used
# Limitation on fishing methods, etc.
- dredge net, Rausu diving equipment, Notsuke spoon net fishery
Regulation on the exercise
[Nemuro]
- dredge net, spoon net or diving equipment, gaff or diving of fishery right
equipment [Abashiri]
- dredge net: up to 2; Tomamai-Haboro: gaff 2-3; Yagishiri: spoon
net: up to 2 [Rumoi]
voluntary regulation
Regulation on the exercise
# Limitation on the scale of fishing gear
of fishery right
- Length of nets: up to 280cm [Ishikari]
- Sawara-Otoshibe: dredge net mesh size: 75mm or larger voluntary regulation
[Watarijima]
- dredge net mesh size: 45.45-75mm; dredge length: 3.18m-4m
[Abashiri]
(iv)Limitation on fishing season
- Yoichi: July 16-March 30; voluntary halt of operation [Shiribeshi]
- Esashi, Kaminokuni area: December, January: harvesting
prohibited
Otobe area: November, December: harvesting prohibited
Taisei(Kaitorima) area: November 21-April 9: harvesting prohibited
Sedana area: January-March: harvesting prohibited [Hiyama]
- Operation season: Yakumo: November 1-March 31 [Watarijima]
- January-May, July-December; voluntary halt of operation
[Hidaka]
- Period for use of dredge net: Wakkanai: March 10-April 30, June
16-September 20; Tombetsu: June 16-August 31; Rirei area: August
1-September 30, Funadomari: November 20-March 31; Kabuka:
November 1-April 30 [Soya]
- Fishing season: Shosanbetsu: July-October; Haboro, Teuri,
Yagishiri, Tomamae: July-August; Onishika: July 1-August 15
[Rumoi]
voluntary regulation
voluntary regulation
Regulation on the exercise
of fishery right
voluntary regulation
voluntary regulation
(v) Limitation on operating hours
- Yakumo: 6:30-noon [Watarijima]
- Soya: until 4: 00 p.m.; Esashi-Wakkanai: return to port by 3: 00
p.m. [Soya]
- Rumoi: no operation every Saturday, operation hour: 9-17
voluntary regulation
[Rumoi]
(vi) Limitation on operation area
- Suttsu: 10 fathoms or shallower: Harvesting prohibited
165
NATIONAL REPORT – MEXICO
Ma. Dinorah Herrero Perezrul.
Centro Interdisciplinario de Ciencias Marinas, Instituto Politecnico Nacional
1. Information on wild populations
a) Species of non-commercial and commercial sea cucumbers in your country´s waters
In México, Isostichopus fuscus is the main target of holothurian fishery in the Gulf of California since the late
80’s. Another sea cucumber, Parastichopus parvimensis is also exploited in the west coast of the Peninsula
of Baja California.
b) Area of distribution, and habitats if known.
Isostichopus fuscus is distributed in shallow waters (0.5 to 40 m depth) from the northern Gulf of California
(30 °N) to Ecuador and the Galápagos Islands, with a Panamic distribution. This holothurian is found in rocky
bottoms and associated to corals, mostly Pocillopora and Porites spp.
c) Abundance.
The abundances of this holothurian range from 0.3 to 0.7 ind/m2 in the Gulf of California and in the Mexican
Pacific from 0.25 to 0.40 ind/m2
2. Nature of sea cucumber fisheries
a) Commercial, artisanal, subsistence.
Isostichopus fuscus is exploited by artisanal fishery, and all the production is exported.
b) Estimated number of fishers
There are currently 8 UMA’s (management units for wild life conservation), which are the only way to extract
the resource. Each UMA works with 3-6 motorized boats (21 feet long). Each boat is operated by the driver
and one or two divers. There can not be more than two divers per boat.
c) Type of fishing methods and gear equipment used
Fishermen use Hookas, (air compressor) and basic dive equipment for the extraction of Isostichopus fuscus,
which are collected by hand and using a net for carrying them to the boat.
d) Licensing and permitting requirements
To date, in Mexico, permits for extraction are denominated UMA (management units for wild life conservation),
on which a management plan is developed for a designated area. After an assessment of the potential populations,
a rational extraction rate is assigned by the authorities (SEMARNAT, Environment and natural resources
secretariat). The license holders must present periodic reports on the activities that enable to control the
appropriate use of the resource. The management plan for this fishery establishes catch quotas in number of
individuals per season rather than weight quotas.
166
e) Sea cucumber farming
There have been several attempts to develop larvae in controlled conditions in the lab, unfortunately they have
not been successful, although we have described the first stages of embryonic development (two cells to early
gastrula).
f) Preferred markets (live vs dried)
All the production is exported to USA and then re-exported to Asian countries. The product is exported dried
after being boiled for two hours approximately for food and traditional medicine
g) Identification of the most important uses of sea cucumbers.
In Mexico holothurian fishery is not a traditional activity and Isostichopus fuscus is not consumed in the
country. However in Ecuador, this sea cucumber is used locally as medicine for respiratory problems, and pain
killers.
h) Landing data (species, bycatch, kg, sizes, etc)
There are two species for export: Isostichopus fuscus and Parastichopus parvimensis.
In 1991, I. fuscus catch reached its maximum peak (about 2,000 metric tones), and then diminished drastically
to 395 mt in 1993 (Table 1). Because of this, the Mexican government banned the fishery in1994 and the
holothurian was considered as an endangered species. This drastic solution had no scientific background, and
in the year 2000 its status changed to a protected species and special permits were emitted. This permits
changed in 2002 to UMA’s, because populations are recovering (at least in the Gulf of California) to allow
rational levels of exploitation. I. fuscus is a large holothurian and they are generally fished between 350 and
450 g and 19 and 25 cm. Since length is highly variable, weight is used to delimit minimum harvesting size,
which is 400 g for this species in the Gulf of California.
On the other hand, Parastichopus parvimensis has been exploited since the early 1990’s, in the west coast
of the Peninsula of Baja California reaching its maximum peak in 1995 (about 600 mt). Despite the fact that
this sea cucumber was exploited with the same intensity as I. fuscus, its populations have remained stable until
the last couple of years, when it is beginning to decline. This situation could be controlled by the establishment
of a management plan, including reproductive bans, which currently is the catch season for this species. There
are no regulations for this fishery at all.
i) Conservation measures (minimum harvesting size, closed areas, closed season, etc)
Isostichopus fuscus is currently considered under special protection in Mexican legislation (NOM-059—
ECOL-2001), but is still extracted on the UMA’s frame. There is a reproductive ban during summer (July to
September), a minimum harvesting size of 400 g, a limited quota in number of individuals. As a precautionary
measure, areas where the smallest specimens were found were closed for extraction, these areas are characterized
by small reefs of Pocillopora and Porites spp and sometimes associated with algae. Ecuador also exploits I.
fuscus and they have already included this holothurian in CITES appendix III.
167
Año
Table 1. Commercial catch of Isostichopus
fuscus in Baja California, Mexico.
3. Domestic and International trade
a)
Information on value, retail,
wholesale prices and trends.
1989
1990
1991
1992
1993
1994
1995
1996
1997
1998
1999
2000
2001
2002
G o lf o d e
C a li f o r n i a
(I. fu sc u s)
336
623
1767
646
395
419
219
58
129
24
36
43
120
20
P a c í f ic o O c c id e n ta l
(P . p a rv im e n sis)
----169
339
469
294
519
421
530
371
247
175
358
286
59
In the early 1990’s sea cucumbers were sold either fresh, boiled or dried. Fresh holothurians were sold at
USD $ 0.65 per kg, boiled (two hours) at USD $30.00 per kg and the dried product was the most expensive,
at USD $60.00 per kg. To this date, the product is sold almost entirely boiled at around USD $12.00 per kg.
All the production is exported to USA, and then re-exported to Asian countries.
b) Export and import volumes, values and trends
As it was mentioned, all the production was and is still exported to foreign countries, but there are no official
data. Mexico does not import sea cucumbers.
c) Information on key sea cucumber trading countries and territories
All the production is exported to USA and then re-exported to Asian countries, mostly Japan, Hong Kong
and Korea. The product is exported dried after being boiled for two hours approximately.
d) Trade controls and enforcement, including identification of specimens in trade.
Authorities emitting export permits (DGVS wild life general administration, SEMARNAT) corroborate that
the catch was legal and under the UMA’s frame and they register all information regarding catch and
exports.
There are no ID manuals to help identify the exportation product, both species are traded as sea cucumber.
e) Information on illegal, unreported and unregulated trade
Illegal fishery has existed previous to the emission of permits for Isostichopus fuscus. This activity continues
to date, this information is presented in Table 2
f) Levels of domestic consumption, trends and trade.
Holothurian fishery is not a traditional activity and all production is exported; there is recent evidence that
some of the product from the UMA’s is being sold locally to restaurants, at an unknown price.
168
NATIONAL REPORT – MALAYSIA
Zaidnuddin Ilias and Kamarruddin Ibrahim,
Turtle and Marine Ecosystem Center, Rantau Abang, Dungun, Terengganu
Introduction
Sea cucumber in Malaysia is known with various terminology for example gamat, balat and timun laut. On the
west coast of Peninsular Malaysia, the term gamat is used to refer to a specific species of sea cucumber which
is the Stichopus horrens. In Malaysia sea cucumber is used in many ways, the Malays used it in traditional
medicine and the Chinese exploit it as delicacies. Sea cucumber was accepted to be highly beneficial in
pharmaceutical industries and studies being done on the chemical components of the sea cucumber especially
the Stichopus horrens. Extraction of the pharmaceutical substances was done from various types of sea
cucumbers found. Samples used were collected from similar morphological body type and from the same area
as the species utilized by the traditional collectors (Figure 1a,b and c).
Collection is still done in Pulau Langkawi as a part time activity for personal consumption during low tides
without using special apparatus in the shallow intertidal reef flats (Baine and Choo, 1999). The sea cucumber
is collected from under dead corals, and rocks by turning it over while wading. The collectors may catch up
from several individuals to a few hundreds normally small fresh sea cucumbers. Collection from wild is the main
and only source of sea cucumber for the industry in Malaysia. Aquaculture, mainly raising wild stock to
marketable size has been tried in some part of Malaysia for example in Sabah and Pulau Pangkor (Yusnizar et
al. 1995). Production of sea cucumber has yet to be tried and succeed in Malaysia.
The main problem faced by the industry is over exploitation, which led to resource depletion. In other part
of the world, over exploitation was the major problem followed by destruction of natural area by pollution
from the development (Erdman, 1995; Kelso, 1996).
Research and Biodiversity
Research on sea cucumber in Malaysia was carried out mainly by Department of Fisheries and the local
universities. Past reports focuses on species density and usage. A short study was carried out by the Fisheries
Research Institute on the possibility of translocation of Stichopus horrens from Pulau Pangkor to Pulau Singa
of Langkawi (Pers. comm.). The study proved successful in techniques utilized for transporting the sea cucumber.
A study was also carried out on the density of Acaudina sp. in the waters of Penang Island and found a high
density area of this species on muddy coastal sea bed of southern Penang (Zaidnuddin, 2001).
Identification of the sea cucumber species is challenging, as there were lack of scientific guide for most of the
sea cucumber (Forbes & Zaidnuddin, 1999). Identification was done from physical body appearance but
problem arises as in certain area the same species may have body taxonomy that is slightly different. A number
of Stichopus sp. found around Malaysian waters were still unidentified to species level but most have been
used for food or medicine (Siti Zaama et al. 1999). On the West Coast of Peninsular Malaysia sea cucumbers
(S. horrens) were collected for traditional medicine and food from Port Dickson, Pulau Sembilan and
Pulauangkor. However in Pulau Langkawi, even though known as one of the producers of sea cucumber
medicine,natural stock of sea cucumber has diminished. Here the sea cucumber supply was imported from
other places.
169
A
Figure 1a: Stichopus sp. at Mersing
Johor Marine Park.
Figure 1b: The red variant of
Stichopus horrens at Pulau Payar
Marine Park
Figure 1c: Sea cucumber wholesaler
C
B
170
Figure 2: Peninsular Malaysia and Sabah surveyed sites
In the year 1999 a conference on “Conservation of sea cucumbers in Malaysia, their Taxonomy, Ecology
and Trade” was held at the Department of Fisheries Malaysia to present a comprehensive summary of the
research undertook by the Heriot-Watt University and the Fisheries Research Institute of Malaysia as part
of the Darwin Initiative for the Survival of Species. It also provided an opportunity for other Malaysian
Universities and fisheries managers to present their results of research projects. It was emphasized that the
problems facing the industry in Malaysia are common to many countries exploiting sea cucumbers (Baine &
Choo, 1999). Through the workshop much progress has been achieved in the three years project promoting
a better understanding of the taxonomy, ecology, fishery and trade of holothurians in Malaysia. Information
on the Malaysian sea cucumber has started to increased through compilation of the research work done by
local and foreign expert.
The Department of Fisheries Malaysia in collaboration with the University of Heriot-Watt has carried out sea
cucumber surveys at Marine Park islands, Sabah and non-marine park islands (Figure 2). From these survey,
distribution of major species was identified. Other studies for example seasonal density variation and gonadal
index were also carried out by other DOF researchers. Seasonal variation of selected species was studied at
two places which were at Pulau Payar and Pulau Tioman. The result shows the fluctuation of the number of sea
cucumber recorded along a permanent transect at Pulau Payar in 1998 (Figure 3). Spawning behaviour of
Stichopus chloronotus was determine using gonad index method showing the spawning behaviour of the
species (Figure 4)
171
Number
20
18
16
14
12
10
8
6
4
2
0
S. horrens
H. atra
H. leucospilota
M
ay
Ju
J
ne uly
N
Au Se
O
D
gu pte ctob ovem isem
st
mb
e
be ber
er r
r
Month
Figure 3: Total number of selected species of Sea cucumber along a
permanent transect at Pulau Payar in 1998
Major progress has been made on the taxonomy and ecology of sea cucumbers in Malaysia. At the end of the
1999 sea cucumber project, some 37 species have been identified, and a few others still remain to be described
as they appear to be new species to science (Table 1)(Forbes et al., 1999). Underwater photographs of the
sea cucumbers and their characteristic habitats have also been compiled. The importance of the sea cucumber
has been overlook for sometimes with the evidence that it has not yet comprehensively describe eventhough
sea cucumber has many large and conspicuous species living in shallow waters.
To enhance research and management activities of marine organisms and protecting it, the Department of
Fisheries has set up a research center for conservation of marine ecosystem named TUMEC, Turtle and
Marine Ecosystem Center in the state of Terengganu. TUMEC functions as a center for marine biodiversity
and conservation. The center was given the task to help the department in conservation and protection of
endangered species.
3. Domestic and international trade
Worldwide trends in fisheries and trade indicate that the number of countries producing beche-de-mer has
recently increased, both in tropical and temperate regions (Conand, 1999). Nevertheless the records for many
countries are incomplete and in some case inaccurate (Baine and Choo, 1999). The situation in Malaysia
appears to be particularly difficult, the country being simultaneously an importer, consumer, producer and
exporter (Baine and Choo, 1999). Nevertheless data is collected by the Department of Fisheries and produced
in the annual fisheries statistic. Recent data shows that the import of sea cucumber for Malaysia exceeded the
export quantity (Figure 5). It will be important to collect and standardize the statistics at the different levels of
the “holothurian system”. It is also vital to emphasize the importance of correct processing methods, to discourage
172
Table 1: The sea cucumber species list (Forbes et al. 1999)
SPECIES
Stichopus chloronotus
S. horrens
S. variegatus
S. noctivagus
S. pseudohorrens
Stichopus hermanni
Stichopus vastus
Thelenota ananas
T. anax
Holothuria coluber
H. atra
H. edulis
H. pardalis
H. verrucosa
H. leucospilota
H. parvicax
H. scabra
H. nobilis
H. fuscopuntata
H. fuscogilva
H. hilla
H. impatiens
Colochirus robustus
Neothynodium violaceus
Cucumaria sp.
Euapta godeffroyi
Synapta maculata
Synaptula media
S. lamperti
Synaptidae sp.indet
Actinopyga echinites
A. leconora
A. miliaris
A. obesa
Bohadschia argus
B. graeffei
B. marmorata
B. paradoxa
4 .0 0
3 .5 0
3 .0 0
Gonad index
2 .5 0
2 .0 0
1 .5 0
1 .0 0
0 .5 0
0 .0 0
Feb 96
M ac 96
Apr 96
M ei 9 6
Jun 9 6
Jul 9 6
O go 9 6
S ep 9 6
O kt 96
S amp ling d ates
Figure 4: Gonad index of Stichopus chloronotus at Pulau Payar in 1996
173
N ov 96
D is 9 6
wastage and improve the profitability of the declining catches. The recent conflicts appearing within or between,
several countries in the region might be interpreted as further signs of overexploitation of the resource, and of
a high level of demand.
Examination of the total import and export of sea cucumber from Malaysia shows that the import of sea
cucumber into Malaysia was always high between 172.53 tonnes to 958.85 tonnes (DOF Statistic 19862001). Nevertheless there are no proves showing the increase in sea cucumber production either from natural
harvesting or aquaculture. Further analysis of the data also shows that the import of sea cucumber is declining
but the export shows an increasing pattern. The export of sea cucumber was low, in 1993 through 1997 less
than 25 tonnes of sea cucumber exported. The import of sea cucumber was high with an average of 565.69
tonnes between 1996 and 2001.
In the year 2001, sea cucumber was imported from various countries mainly Hong Kong (100.2 tonnes),
Japan (151.26 tonnes), Korea, Singapore, Taiwan and Thailand (DOF, 2001)(Figure 6). This gave Malaysia
a total expenditure of RM 4.9 million from a total import of 403.27 tonnes of sea cucumber. On the other hand
the export of sea cucumber from Malaysia was 158.41 tonnes with a total of RM 1.9 million revenue (DOF,
2001).
The management of sea cucumber resources has to be approached on locality basis and appropriate controls
should be put in place for each region. Development of fishery regulations should focus on stocks consisting
monitoring and effective enforcement. The threats on stocks of sea cucumbers in Malaysia were confined to
the Stichopus horrens of Pulau Langkawi and the west coast of Peninsular Malaysia while in Sabah the
targeted species were the larger size sea cucumbers. Other more abundant species for example the Holothuria
atra, Stichopus chloronotus and H. leucospilota were not targeted in Malaysia. Better and proper management
strategies should be focused on these targeted species. At present the use of sea cucumber is not limited to
traditional medicine but also processed in scientific ways to produce food supplement (Figure 7)
The problems facing the Malaysian sea cucumber industry are complex. Development of a regional network,
dealing with the same set of fisheries problems, species and management controls is a desirable need.
Broadercommunication between parties can be of benefit to the environment and industry. It would help
disseminate the information on the issues an also help others to avoid making the same mistakes, promote
research and recovery of stocks.
There is a growing concern, surrounding trade between bordering country for example Malaysia, Thailand,
Indonesia and Phillipine, that requires a concerted collaborative effort from Malaysia and the neighbouring
country (Baine and Choo, 1999). The potential for overfishing in Thailand waters is high, given the evidence of
levels of trade to Pulau Langkawi combined with observations on the widening geographical focus of Thai
fishers within their own territory to meet the demand within Pulau Langkawi. The potential for overfishing and
subsequent possible domino effects in Malaysia, such as the development of an intensive fishery in the waters
off the west coast of peninsular Malaysia (for example Pulau Pangkor) in order to meet the demand can be
detrimental. This situation should be addressed appropriately and requires immediate attention.
In Pulau Langkawi and Sabah an extensive infrastructure has developed (fishers, processor and traders)
(Figure 8)around holothurian fisheries (Baine and Choo, 1999). Although this may not contribute significantly
to the country’s economy, there are important source of income for small coastal and island communities which
cannot be ignored. In the Pulau Langkawi for example, there are more than 100 local families involved in sea
cucumber medicine production line from producer to trader on which some depend on it as a main source of
income.
174
4. Conservation effort
Effort to conserve the resources started due to the depletion of the natural resources in some part of Malaysia.
The Department of Fisheries has started a study on S. horrens in early 1993 and also tried a translocation
program. Nevertheless it was clear that further studies were needed on different aspects of the sustainable
exploitation of sea cucumbers in Malaysia. For that purpose a study was also carried out to identify the sea
cucumber species was carried out by DOF in collaboration with a local university in 1994. This was then
followed by a three years collaboration project with Heriot Watt University under the Darwin Initiative funding.
These studies mainly focus on biology and ecology of the species in Malaysia and also the possibility of
aquaculture production.
The sustainable exploitation of sea cucumbers from the area will be dependent on a better understanding of the
resources available in the country and it threats. Unfortunately, the life-history traits and the population ecology
of many of the commercial species have not yet been intensively studied in the region. Worldwide there is very
little data available on recruitment, growth and mortality for most species. In general, it appears that many
commercial species are slow-growing and very vulnerable to over exploitation. Research into population
dynamics and stock assessments are also needed, even though the resource seems to be already severely
depleted in some areas. The variable nature of the fishery indicates that management solutions will differ
between areas depending on the degree of over-exploitation. There may be future cause for concern for a
fishery that targets juveniles. On the other hand the situation in Pulau Langkawi and Sabah, demands immediate
mobilization of Department of Fisheries resources.
Research, education and extensive knowledge are needed for the best conservation effort. Action for example
total prohibition of specific species, creating sanctuaries for sea cucumber, aquaculture production and restocking
the wild are some of the actions to be considered. One of the appealing management options is restocking sea
cucumbers stock with juveniles produced in hatcheries. Hatchery production techniques are now available for
only one tropical species, the high value sandfish, Holothuria scabra (Battaglene, 1999). Restocking sandfish
and potentially enhancing stocks above historical harvest levels is a priority area for research but does not
currently offer an immediate solution to the declining stocks of the most commonly exploited species in Malaysia.
Other action for example farming of sea cucumbers is practiced in China, Indonesia and India but not yet in
Malaysia. Grow-out of cultured sandfish in cages or enclosures may be another alternative way for fishermen
to provide product for processors. It may also elevate pressure on natural stocks.
Research on culture aspects of Stichopus horrens should be emphasized as this is the target species for local
consumption, industrially produced food supplement and traditional medicine. Success in production of these
species will be of benefit to the local public and the conservation of threatens sea cucumber species.
There is growing interest in the potential for culture and restocking of juveniles holothurians. This should be
approached with cautions, as this is not the ultimate answer to all holothurian’s management problems, indeed
there is still considerable research to be undertaken into refining basic premises behind their rearing and stocking.
175
5. Monitoring and Enforcement
Enforcement of sea cucumber conservation strategies require good data and proper authority for this is the
marine park section of the Department of Fisheries and the research section. Proper training of the staffs prior
to the collection of the data and monitoring is vital. Staffs have to be trained in diving survey methodology and
holothurian’s taxonomy. The knowledge should be utilised to the full in the monitoring surveys within the
conservation area and other area under the jurisdiction of the Department of Fisheries. This will result in a
constant supply of extensive field data on species presence, their temporal and spatial distribution, and growth
(length and weight analyses). This will enable future research to interpret comprehensive information available
in the form of a well established database on stock dynamics. At present, the research wing of the Department
of Fisheries carries out monitoring and study of the marine organism. The marine park islands provide ideal
areas for future research on other aspects of holothurian reproductive biology and ecology. Trained marine
park personnel can also be utilized within such research and they can be trained in SCUBA, survey and
taxonomy techniques (Forbes and Zaidnuddin, 1999).
Holothurian taxonomy is currently in confusion with many reviews going on. It is important that the monitoring
programme maintain adequate photographic and morphological records. The monitoring should also incorporate
examination of spicule distribution and composition within different holothurian species and at varying stages of
their life cycle.
An integrated approach to holothurian fisheries management in Malaysia should be carried out not only in
research and regulation but in its widening of scope to involve other countries in SE Asia with a view to
approach a common problem that already sees a maze of existing international trade links.
6. Legal and Fisheries Act
At present the Fisheries act gazetted 25 species of marine organisms; Dugong, whale, dolphin, whale shark
and giant clams as endangered and protected (Control of endangered fish species, DOF, Fisheries Act P.U.(A)
1985) . Legally the sea cucumber in Malaysia is not protected specifically under Fisheries Act or Marine Park
act. The sea cucumber species within the boundary of Marine Park is protected but harvesting outside of the
park is legal.
Promoting the fisheries act to protect the sea cucumber species in Malaysia is possible now as there are strong
indications of high exploitation of resource and probable case of stock depletion. There are many potential
approaches to the problems and opportunities unearthed by past research. Possible options for direct
management of sea cucumber might be the application procedures adopted elsewhere including the setting of
minimum landing sizes, establishing closed areas and seasons and even complete prohibition of fishing. Sabah
state is the area that may most require such regulation, but the following points must be considered (Baine and
Choo, 1999):
•
•
•
Preparation of baseline data for the fishery;
Determining associated political and social repercussions that may arise;
The lack of resources within the Fisheries Department to enforce regulations in a fishery which is not
seen as priority for internal management.
176
1200
1000
total import
Total export
Tonne
800
600
400
200
20
00
19
98
19
96
19
94
19
92
19
90
19
88
19
86
0
Year
Figure 5: Total import and export of sea cucumber from Malaysia in
various forms (Source Baine & Choo, 1999; Department of Fisheries
Malaysia 1986-2001 Statistics
17.52 2.4
46.77
1.62
100.2
84.5
Hong Kong
Japan
Korea
Singapore
Taiwan
Thailand
Indonesia
151.26
Figure 6: Countries exporting sea cucumber to Malaysia (DOF 2001) value in tonne
177
Acknowledgements
The authors would like to thank the Director General of Fisheries Malaysia, Darwin Initiative, The Marine
Park Division, Director of Research and others who help make this paper come through.
Reference
Yusnizar,Y., Awaluddin, A., Kadri, A. and Mustafa, S. (1995) Kajian kesan pemakanan ke atas tumbesaran
timun laut (Holothuria scabra Jaeger) yang di kultur sangkar di Teluk Ambong, Kota Belud Sabah. Proc.
Coll. Sumber Alam UKM(Sabah) 3:8
Erdmann, M. 1995. An ABC guide to coral reef fisheries in Southwest Sulawesi, Indonesia. In. Naga, The
ICLARM quarterly, April 1995: 4-6
Kelso,B.J. 1996. Warning signs unheeded in South Pacific invertebrate trade. In. Naga, The ICLARM
quarterly, January: 9-12
Baine, M. and Choo,P.Z.(1999) Sea cucumber fisheries and trade in Malaysia. In, Baine, M. (ed) 1999. The
Conservation of Sea cucumbers in Malaysia: their taxonomy, ecology and trade. Proceeding of an International
Conference, Ministry of Agriculture, Department of Fisheries, Kuala Lumpur Malaysia: 49-64
Siti Zaama, R.B., Zulfigar, Y. and Tan, A.S.H. (1999) Species of sea cucumber found in Pulau Besar, Johor,
with special emphasis on the genus Stichopus. In, Baine, M. (ed) 1999. The Conservation of Sea cucumbers
in Malaysia: their taxonomy, ecology and trade. Proceeding of an International Conference, Ministry of
Agriculture, Department of Fisheries, Kuala Lumpur Malaysia: 11-26
Forbes, R.(main), Ilias,Z.,Baine,M.,Choo,P.S. and Wallbank,A. 1999. Ataxonomic key and guide to the sea
cucumbers of Malaysia. Pub. Heriot-Watt University. 62p, ISBN 0-9531575-4-7
Forbes, R. and Zaidnuddin I.(1999) The Taxonomy and Ecology of Sea Cucumbers in Malaysia. In, Baine,
M. (ed) 1999. The Conservation of Sea cucumbers in Malaysia: their taxonomy, ecology and trade.
Proceeding of an International Conference, Ministry of Agriculture, Department of Fisheries, Kuala Lumpur
Malaysia: 42-49
Conand, C.(1999) World Sea Cucumber Exploitation and Market For Trepang: An Overview. In, Baine, M.
(ed) 1999. The Conservation of Sea cucumbers in Malaysia: their taxonomy, ecology and trade. Proceeding
of an International Conference, Ministry of Agriculture, Department of Fisheries, Kuala Lumpur Malaysia:
1-10
Department of Fisheries Statistics (2001).
Zaidnuddin, I. (2001) Sea cucumber species diversity and abundancefrom the south-western waters of Balik
Pulau, Penang. Workshop on the impact of development on the coastal fisheries off south-west Penang
Island 7-8 June 2001, Fisheries Research Institute, 11960 Batu Maung, Penang, Malaysia: 57-62
178
Figure 7: New product from sea cucumber (Stichopus horrens)
179
Figure 8: Processing sea cucumber before selling
180
NATIONAL REPORT – THE PHILIPPINES
Ludivina L. Labe
BFAR/National Fisheries Research & Development Institute,
CITES Scientific Authority for Aquatic Species, Philippines.
1. Information on wild populations
a. Non-commercial and commercial species, distribution and habitats.
The holothurians (Echinodermata: Holothuroidea), commonly known as sea cucumbers, once abound in nearly
all the shallow-water reef areas of the Philippines (Clark and Rowe, 1971; Schoppe, 2000) (Fig. 1). Of the
approximately 1400 described species worldwide, about 100 species of Philippine holothurians have been
recorded by past distribution and taxonomic accounts. Recent surveys have accounted 41 species belonging
to five families around the provinces of Pangasinan, northern Luzon; Batangas, Mindoro and Palawan in
southern Luzon; Bohol and Negros Occidental in central Visayas; Leyte, eastern Visayas and Zamboanga,
northern Mindanao (Colin and Arneson, 1995; Gosliner, et al., 1996; Carpenter and Niem, 1998; Schoppe, et
al., 1998; Schoppe, 2000). They abound in all habitat types: sandy, mudflats, reef flats and lagoons (Table 1).
Colin and Arneson (1996) recorded the world’s largest sea cucumber, Stichopus variegatus measuring 39 x
9.5 inches from the Philippines. About 30 commercial species in the families Holothuriidae and Stichopodidae
are being utilized as food source for domestic and international markets (Roa, 1987, Ferrer, 2001) (Table 2).
b. Information on abundance.
The present status of the resource is unknown due to the absence of statistical monitoring in the once rich areas
of the country (Schoppe, 2000; Gamboa, et al., 2003). The increasing depletion of natural stocks is obvious
based on these reports, the available fisheries data and anecdotal accounts. Collection sizes of commercial
species are reportedly getting smaller and the collection sites, which were for many years within the littoral
zone, have now moved to deeper waters (Roa, 1987; Schoppe, 2000). The accessibility of the collection sites
of commercial species and the high demand for the products particularly in the world markets make the
resource vulnerable to over-exploitation. There is a current move by the research staff of the National Fisheries
Research and Development Institute (NFRDI), which is the research arm of the Bureau of Fisheries and
Aquatic Resources (BFAR) to conduct studies on the natural population and catch statistics of sea cucumbers
for conservation and management purposes.
2. Nature of sea cucumber fisheries
a. Artisanal fisheries.
The advent of sea cucumber fisheries in the Philippines dates back to c1911 (Roa, 1987). The methods of
collection and equipment used remained the same through the years as reported by various authors. In 1995,
this author had the personal experience of observing holothurian collection and processing in an island village in
Bohol, central Visayas. The commercial species in the families Holothuriidae and Stichopodidae are heavily
collected by gleaning during low tide by members of fishing families in coastal villages all over the country. The
deep-water species are collected by diving from small boats by divers using improvised air compressor or
“hookah” (Table 1). These species are known by various local names based on the distinctive external
characteristic of the animal (Table 2). The works of Alcala and Alcazar (1984), Roa (1987) and Schoppe
(2000) gave glimpses on the status of sea cucumber fisheries in selected areas. The frequently collected
species are Holothuria scabra, Bohadschia marmorata, Actinopyga lecanora, Holothuria fuscocinerea,
Holothuria atra and Stichopus hermanni (Schoppe, 2000).
181
Table 1. Commercial and non-commercial species of sea cucumbers in Philippine waters and methods of
collection of commercial species. (Source: Colin & Arneson (1995); Gosliner, Behrens & Williams (1996);
Carpenter & Niem (1998); Schoppe (2000).
S C IE N T I FI C N A M E
E N G L IS H N A M E
D IS T R IB U T IO N
M ETHO D OF
C O L L E C T IO N
H O L O T H U R IID A E
Ac tino py ga leca no ra (Jaeger, 1 83 3)
E ast A frica; M ad ag asca r to
A u stralia; N e w C aled o n ia;
In do n esia; P hilipp ine s;
so u th ern Jap an
g le an ing
Ac tino py ga ech inites (Jaeg er, 1 83 3)
*
D eep -w a te r red fish
In do -W est P acific fro m
Z an zib ar ea st to so uth ern
C h in a; th e R yu kyu Islan d s;
P h ilip p in es; E ast Ind ies ; F iji
an d no rth ern A us tralia
g le an ing
Ac tino py ga m au ritian a (Q u o y &
G aim ard , 1 83 3) *
S u rf red fis h
W ide spread in the tro p ic al
In do -P acific
g le an ing
Ac tino py ga m iliaris (Q u o y &
G aim ard , 1 83 3) *
H airy b lack fish
W ide spread in the pro pic al
In do -P acific in clud ing the
R ed S ea b ut ex clu din g the
P ersian G u lf a nd H aw aii
g le an ing
Ac tino py ga ob esa (S elen ka, 18 67)
Bo h ad sch ia a rg us Ja eger, 1 83 3
S o lo m o n Island s;
P h ilip p in es; C h in a an d
H a w aiian Islan ds
Le op ard fis h
d ivin g
R ed S ea; M ald ives to
A u stralia; N e w C aled o n ia;
N e w G uin ea ; In d on esia a nd
P h ilip p in es; M ad ang ; P N G
Bo h ad sch ia g ra effei (Se m p er,
18 68 )
Bo h ad sch ia m a rm o ra ta Jaege r,
18 33
S e ych elles to A u stralia; N e w
C ale do n ia; In do n esia;
M ala ysia; P h ilip pin es an d
n o rth ern Jap an
C h alk y se a cu cu m b er
Bo h ad sch ia p ar ad oxa (S elen ka,
18 67 )
T hro u gh ou t th e In do -W est
P acific e xclu d ing th e
H a w aiian Islan ds
d ivin g
A u stralia; P h ilipp in es to
H a w aiian Islan ds (M a ui)
Bo h ad sch ia v itie nsis (S em pe r,
18 67 )
B ro w n san d fish
W ide spread in the tro p ic al
In do -P acific
g le an ing /div ing
Pe ar son o th u ria g rae ffei (S em p er,
18 68 )
B lack spo tted sea
cu cu m be r
W ide spread in the tro p ic al
In do -P acific, exclu d in g th e
P ersian G u lf & H aw aii
d ivin g
H olo thu ria (H a lo de im a ) a tra
Jaeg er, 1 83 3
lo llyfish
T hro u gh ou t th e tro pica l
In do -w est P ac ific
g le an ing /div ing
H olo thu ria (H a lo de im a ) edu lis
Lesso n , 1 83 0
P in kfish
W ide spread in the tro p ic al
In do -P acific; exclu d in g
H a w aii
g le an ing
H olo thu ria (H a lo de im a ) pu lla
H olo thu ria (A ca n tho trap eza )
co lu b er S em p er, 18 6 8
E ast A frica an d M ad agasc ar;
E ast In d ies; P h ilip pin es a nd
th e S ou th P acific Islan d s
S n ake fish
W ide spread in the tro p ic al
P acific , e xclu d in g H aw a ii;
n o t reco rd ed in the In dia n
O c ean
182
g le an ing /div ing
SCIENTIFIC NAME
ENGLISH NAME
METHOD OF
COLLECTION
DISTRIBUTION
Holothuria (Microthele) fuscogilva
Cherbonnier, 1980
White teatfish
Widespread in the tropical
Indo-Pacific
diving
Holothuria (Microthele)
fuscopunctata Jaeger, 1833
Elephant trunkfish
Australia; New Caledonia;
New Guinea; Belau; the
Mariana Islands; Philippines
diving
Holothuria (Microthele) nobilis
(Selenka, 1867)
White teatfish
Widespread in the tropical
Indo-West Pacific
gleaning/diving
Holothuria (Microthele) whitmae
Teatfish; mammy
blackfish
Throughout the tropical
indo-West Pacific
Holothuria (Thymiosycia) hilla
Lesson, 1830
Throughout the Indo-West
Pacific
gleaning
Holothuria (Thymiosycia)
impatiens (Forskal, 1775)
East Africa; Red Sea to the
Hawaiian Islands; tropical
Atlantic; Mediterranean
gleaning
Western Indian Ocean and
Red Sea; western Pacific to
the Hawaiian Islands (Cook
Islands)
gleaning/diving
Holothuria (Cystipus) inhabilis
SE Arabia; China;
Philippines; East Indies;
Pacific Islands; Australia
gleaning/diving
Holothuria (Cystipus) rigida
(Selenka, 1867)
East Africa to Hawaii;
western coast of North
America; Panamanian
Region; Galapagos and the
West Indies
Holothuria (Mertensiothuria)
leucospilota (Brandt, 1835)
White threadfish
Holothuria (Metriatyla) scabra
Jaeger, 1833
Sandfish
Widespread in the IndoPacific excluding Hawaii
gleaning
Holothuria (Metriatyla) scabra var.
versicolor (Conand, 1986)
Sandfish
Widespread in the tropical
Pacific, excluding coral reef
islands
gleaning
Stichopus chloronotus Brandt, 1835
Greenfish
Widespread in the tropical
Indo-Pacific excluding the
Persian Gulf
gleaning/diving
Stichopus hermanni
Curryfish
Throughout the tropical
Indo-West Pacific except the
Hawaiian Islands
gleaning/diving
Stichopus horrens Selenka, 1835
Selenka’s sea
cucumber
Widespread in the tropical
Indo-Pacific
gleaning/diiving
STICHOPODIDAE
Stichopus noctivagus Cherbonnier,
1980
New Caledonia; New
Guinea; Philippines and
Hawaiian Islands
183
Table 1. Continued
SCIENTIFIC NAME
ENGLISH NAME
DISTRIBUTION
METHOD OF
COLLECTION
Stichopus variegatus Semper,
1868
Curryfish
Widespread in the tropical
Indo-Pacific excluding
Hawaii
gleaning
Thelenota ananas (Jaeger,
1833)
Prickly redfish;
pineapple sea
cucumber
Widespread in the tropical
Indo-Pacific, excluding
Hawaii
diving
Thelenota anax Clark, 1921
Amberfish; giant
beche-de-mer
In the tropical Indian
Ocean; in the tropical
Pacific; from northern
Australia to Enewok,
Guam, China Sea and
Ryukyu Islands
southwards to New
Caledonia, Fiji and the
Society Islands
diving
New Guinea; Solomon
Islands; Guam; Banda
Islands; New Caledonia;
Philippines; Indonesia;
SCS; Fiji & Palau
diving
Thelenota rubralineata Massin &
Lane, 1991
CUCUMARIDAE
Colochirus robustus Ostergren,
1898
Indonesia; Belau and
Philippines
Cucumaria miniata
Indonesia; Palau;
Philippines (Pamilacan Is)
Neothyonidium magnum
(Ludwig, 1882)
Western Pacific; New
Caledonia; New Guinea;
Indonesia; Philippines
Pseudocolochirus violaceus
(Theel, 1886)
SYNAPTIDAE
India; northern Australia
and Philippines
Euapta godeffroyi (Semper,
1868)
Sticky snake sea
cucumber
Throughout the Indo-West
Pacific
Opheodesoma grisea (Semper,
1868)
Serpent synaptid
East Africa and the Red
Sea to Hainan Island;
Philippines; the East
Indies and Hawaiian
Islands
Synapta maculata (Chamisso &
Eysenhardt, 1821)
Maculated synaptid
Throughout the Indo-West
Pacific excluding the
Hawaiian Islands
Synaptula media Cherbonnier &
Feral, 1985
New Caledonia; New
Guinea; Micronesia and
Philippines
184
b.Number of fishermen and landing data
Due to the scarcity of fisheries data, the number of fishermen who depend on sea cucumber fisheries for
livelihood is unavailable. However, historical data on sea cucumber production based on landed catches from
artisanal fisheries are on hand until 1997. The usefulness of these historical catch data in conservation and
management initiatives is diminished by the inability of field workers to identify the landed catch and processed
products to species level. The latest available data shows fluctuating annual landed catch from as high as 3109
metric tons in 1993 to a low 1191 metric tons in 1997 (Figure 2). Ferrer (2001) conducted a study of artisanal
fisheries in Danao, Misamis Occidental on the island of Mindanao. Based on data collected from the fishers
and historical catches in Danao Bay, the fishers could only collect 0.5 kg of live weight per hour in 1997,
compared to 100 kg/hr in 1960s and 1980s.
c. Licensing and permitting requirements
In most municipal waters, there is the so-called “open access” in the utilization of marine resources. In some
areas, however, the local government unit, which has jurisdiction over the coastal waters, issues a “license or
permit to collect” with validity of three years to the fisherfolks engaged in the collection or stakeholders. This
permitting requirement is not in any way a form of regulation or control in the use of the resource as the license/
permit is issued to all applicants. Moreover, not all local government units in the country require the stakeholders
to secure such license/permit (BFAR-FRQD, pers. comm.)
d. Sea cucumber farming
Sea cucumber culture in the Philippines is still in its infancy with initiatives coming from academic institutions.
Grow-out culture and seedstock production of the highly valued Holothuria scabra is being done at the
marine laboratory of the University of the Philippines Marine Science Institute with the primary purpose of
reseeding marine protected areas (MPAs) (Gamboa, et al., 2003). It is hoped that commercial quantities of
seedstock will become available in the future for interested entrepreneurs and relieve the pressure on natural
population.
e. Most important uses of sea cucumbers
Besides being high value commodity as food source, the pharmaceutical potential and other commercial uses
of sea cucumbers are being discovered. The processed products were found to have curative powers for
ailments like high blood pressure and muscular disorders. Cuvierian tubules are being used as crude plaster for
minor wounds (Roa, 1987). The scientists from the University of the Philippines in Los Banos, Laguna have
found the chloroform extracts called lectins from Holothuria nobilis, H. axiologa, Bohadschia marmorata
and Stichopus chloronatus as having promising anticancer and antibacterial activity (Mojica, et al., 2003).
f. Conservation measures
Philippine sea cucumber fishery depends solely on natural stocks. At present, there are no laws governing the
exploitation and utilization of the commercial species. The local government units have the authority to draft
and pass conservation measures, e.g. limited access, closed seasons, and closed areas, minimum harvestable
size, in the form of municipal ordinance with or without scientific bases for such measures. The dearth of best
available data on their population and ecological status in Philippine waters is primarily due to budget constraints
on scientific research, while the “precautionary approach” to conservation seems not a popular option in the
absence of scientific bases.
185
Table 2. Prices of sea cucumber species (US$1.00 = PHP 56.00) (Source: modified from Schoppe, 2000)
SCIENTIFIC NAME
LOCAL NAME
PRICE/kg (US$)
Actinopyga echinites **
brown beauty; khaki
20.5
Actinopyga lecanora ***
buli-buli; monang/manang
37.00
Actinopyga mauritiana ***
bakungan
31.00
Actinopyga miliaris **
khaki
26.00
Bohadschia argus **
leopard; matang itik
23.50
Bohadschia marmorata **
lawayan; pulutan
22.50
Holothuria atra **
black beauty
21.00
Holothuria edulis **
red beauty
21.00
Holothuria coluber *
patola white; tambor
16.50
Holothuria fuscocinerea *
labuyo
17.38
Holothuria fuscogilva *
patola
16.76
Holothuria fuscopunctata *
sapatos
18.00
Holothuria leucospilota **
patola
20.75
Holothuria nobilis ***
susuan
41.00
Holothuria inhabilis *
batunan
local consumption
Holothuria pulla **
patola red
Holothuria rigida *
batunan
Holothuria scabra ***
kurtido; putian
41.00
Holothuria scabra var. versicolor *
kurtido bato
16.50
Holothuria whitmae ***
susuan
41.00
Pearsonothuria graeffei *
pina; hanginan; mani-mani
17.75
Stichopus hermanni ***
hanginan
37.25
Stichopus horrens ***
hanginan
37.25
Stichopus variegatus **
hanginan; gadul
20.20
Thelenota ananas **
talipan; taripan
28.50
Thelenota anax **
legs
20.25
21.00
local consumption
186
Figure 1. Philippine map showing the sea cucumber collection and processing areas
187
Sea cucumber production 1993-1997 (in m etric ton)
3500
3109
CATCH (metric ton)
3000
2500
2123
2062
2000
1497
1500
1191
1000
500
0
1993
1994
1995
1996
1997
YEAR
Figure 2. Municipal production of sea cucumbers, 1993-1997 (MT)
Volume of Export (metric
ton)
Dried sea cucumber export 1993-2001 (in m etric ton)
2500
2049
2000
1692
1565
1692
1459
1500
1384
1297
1040
1270
1125
1000
500
0
1992 1993
1994
1995 1996
1997
1998
1999
2000 2001
Year
Figure 3. Export volume of dried sea cucumbers 1992-2001 (MT)
Export Value (million P)
Export value of dried sea cucumber 1993-2001 (m illion P)
300
266
285
250
200
150
100
108
107
1993
1994
124
126
147
135
99
82
50
0
1992
1995
1996
1997
1998
1999
2000
2001
Year
Figure 4. Export value of dried sea cucumbers 1992-2001 (millionP)
188
3. Domestic and international trade
a. Domestic trade
In the Philippines, the trade in sea cucumbers involves the fisherfolks, middlemen and exporters as key players.
After collection, the cleaning and processing of gutted sea cucumbers into fresh/frozen, dried and smoked
products are carried out by the collectors themselves or brought to processors in their respective areas. The
processed products are deposited in designated trading places within the community until a commercial volume
is reached (BFAR FRQD, pers. comm.). The existence of sea cucumber fisheries and processing has been
confirmed in northern Luzon provinces of Pangasinan, La Union and Cagayan; eastern Luzon province of
Zambales; southern Luzon provinces of Quezon, Batangas and Palawan; central Visayas provinces of Cebu,
Bohol and Negros Occidental; The middlemen from different parts of the country have the knowledge of the
trading season in each locality and have complete control over domestic prices. The prices of processed
products depend on the size (small, medium, large) or grade (class A, B, C). From the fisherfolk collectors to
middlemen, trading shifts hands from the middlemen to local businessmen who are engaged in the supermarket,
hotel, restaurant and export businesses (Gamboa, et al., 2003). The prevailing domestic price of sea cucumbers
is unavailable.
b. International trade: export volume and trends
The international market is dominated by dried sea cucumber products with the Philippines as the 2nd major
producer and exporter. From 1997 to 2001, dried sea cucumbers ranked 8th in the country’s top 10 major
export commodities (BAS, 2002). The markets in Asia receive the bulk of dried products from all exporting
countries. Philippine export statistics show a decline in export volume from 2049 tons in 1993 to 1125 in 1999
with slight increase in 2000 (1692 tons), and then dropped to 1270 tons in 2001 (Fig. 3). The decline in the
volume of export may be the result of the Asian economic crisis in the late 1990s or low supply from exporting
countries due to over-exploitation of high priced species such as Holothuria scabra, Stichopus spp., Holothuria
nobilis, H. whitmae and Actinopyga lecanora (Roa, 1987; Schoppe, 2000).
c. Export values
Despite the recession and low supply of commercial species, there is a steady increase in prices of processed
products. The exported dried sea cucumber in 1992 was valued at PHP 82 million and increased to PHP 285
million in 2001 (Fig. 4). The most recent trading prices from the traders in Palawan, southern Luzon was
obtained from Schoppe (2000). The prices of high value species ranged from US$ 8.75 to 25.00 per kg of dry
weight with exchange rate of PHP 40.00 to US$ 1.00. These figures increased by more than 71% with the
current exchange rate of PHP 56.00 to US$ 1.00 (Table 2).
d. Trading countries and territories
Asia is still the biggest market for dried sea cucumber from the Philippines. At least five exporters are regularly
supplying the markets of China, Hong Kong, Taiwan, Singapore, Malaysia, Korea and Indonesia. Canada is
the only trading partner outside of Asia (BAS, 1996 and 2002). The breakdown of the annual export volume
and value are not available from the current statistics.
189
e. Trade controls, enforcement and identification of traded specimens
Traders and middlemen of sea cucumber products are required to secure quarantine clearance from the
Regulatory and Quarantine Division of the Bureau of Fisheries and Aquatic Resources (BFAR) regional field
office at the point of origin when transporting the commodity within the country. The clearance, which is being
issued free of charge, contains the generic/common name and volume of the products to be transported.
Sea cucumber products intended for the foreign markets should be accompanied by an export commodity
clearance, duly signed by the fisheries officer and all trade-related agencies at the One Stop Export Processing
Center. The commodity clearance likewise contains the generic name (scientific name, whenever possible),
English and local name and volume of the products. Identification of specimens from the landed catch and
processed products for trade is only up to family level as field enumerators and quarantine officers have limited
knowledge about sea cucumber identification, particularly of the processed products (BFAR FRQD pers.
comm.).
f. Illegal, unreported and unregulated trade
The collection and trade in Philippine sea cucumbers are unregulated. Likewise, there is greater possibility of
non-compliance with the permitting procedure by some exporters. This is likely the situation in countries where
there is open access to resources and the absence of any conservation measure.
g. Levels of domestic consumption, trends and trade
Sea cucumbers are not a basic food source of Filipinos, but fresh meat is a delicacy in coastal villages. The
fresh/frozen, dried and smoked sea cucumber products are being marketed locally in supermarkets and form
part of cuisines in local hotels and restaurants (Roa, 1987; Gomez et al., 2003). The bulk of processed
products, particularly the dried and smoked forms are intended for the export markets where they remain in
demand and high value products (Roa, 1987, Schoppe, 2000).
190
References
Bureau of Agricultural Statistics. 1998 and 2002. Fisheries Statistics of the Philippines. Quezon City: DA/
BAR.
Bureau of Fisheries and Aquatic Resources, Fisheries Regulatory and Quarantine Division (personal
communication).
Carpenter, K.E. and V.H. Niem (Eds.). 1998. Living marine resources of the Western Central Pacific. Vol. 2.
Cephalopods, crustaceans, holothurians and sharks. FAO Identification Guide for Fishery Purposes.
Rome: UN/FAO.
Clark, A.M. and F.W.E. Rowe. 1971. Monograph of shallow-water Indo-West Pacific echinoderms. London:
Trustees of the British Museum (Natural History). 269p.
Colin, P.L. and C. Arneson. 1995. Tropical Pacific Invertebrates: a field guide for the marine invertebrates
occurring on tropical Pacific coral reefs, seagrass beds and mangroves. USA: The Coral Reef Research
Foundation. 297p.
Deocaris, C.C., M. Altamia, C. Saloma. 2003. Fluorescent proteins in sea cucumbers. In: 7th National
Symposium in Marine Science, 22-24 October 2003. Manila: The Philippine Association of Marine
Science, Inc.
Ferrer, E.M. (ed.) 2001. Hope takes root: community based coastal resources management stories from
Southeast Asia.
Gamboa, R., L. Gomez, M.F. Nievales, H.G. Bangi and M.A. Menez. 2003. The status of sea cucumber
fisheries and mariculture in the Philippines. In: 7th National Symposium in Marine Science, 22-24
October 2003. Manila: The Philippine Association of Marine Science, Inc.
Gosliner, T.M., G.C. Williams and D.W. Behrens. 1996. Coral reef animals of the Indo-Pacific: animal life from
Africa to Hawaii exclusive of the vertebrates. CA: Sea Challengers. 314p.
Leonardo, L.R. and M.E. Cowan. 1984. Shallow-water holothurians of Calatagan, Batangas, Philippines.
Quezon City: Filipinas Foundation.
Mojica, E., R.J. Layson, M.C. Rodil, C.C. Deocaris. 2003. Anticancer and antibacterial activities of echinoderm
extracts. In: 7th National Symposium in Marine Science, 22-24 October 2003. Manila: The Philippine
Association of Marine Science, Inc.
Nievales, M.F. and M.A. Juinio-Menez. 2003. Effect of stocking density and substrate addition on growth
and survival of hatchery produced Holothuria scabra juveniles. In: 7th National Symposium in Marine
Science, 22-24 October 2003. Manila: The Philippine Association of Marine Science, Inc.
Schoppe, S. 2000. A guide to common shallow-water sea stars, brittlestars, sea urchins, sea cucumbers and
feather stars (Echinoderms) of the Philippines. Singapore: Times Media Pty. Ltd. 144p.
Schoppe, S. 2000. Sea cucumber fishery in the Philippines. SPC Beche-de-mer Information Bulletin #13
Schoppe, S., P.P. Gatus and M.R. Seronay. 1998. Gleaning activities on the islands of Apid, Digyo and
Mahaba, Inopacan, Leyte, Philippines. Phil. Scient. 18: 130-140
Tan Tiu, A. 1981. The intertidal holothurian fauna (Echinodermata: Holothuroidea) of Mactan and the neighboring
islands, Central Philippines. Phil. Scient. 18: 45-118.
Roa, M.J.T. 1987. Beche-de-mer fishery in the Philippines. NAGA, the ICLARM Quarterly, Oct. 1987: 1517.
191
Sea Cucumber Population Status, Fisheries and Trade in the United States
Andrew Bruckner
NOAA Fisheries, U.S. Department of Commerce
1. Information on wild populations
A) Tropical
i) Western Atlantic
There are seven sea cucumbers of potential commercial value in the waters surrounding Florida, Puerto Rico
and the U.S. Virgin Islands (Astichopus multifidus, Actinopygia agassizii, Isostichopus badionotus,
Eostichopus amesoni, Holothuria mexicana, H. thomasae, and H. impatiens). These occur in mangrove,
grassbed, coral reef and sandy or silty environments. All species are most common from about 1 m to 10 m
depth, except A. multifidus which is most common from 5-40 m depth. These species generally occur at
densities of up to 1-2 animals per 10 m2. Higher densities are occasionally observed for some species. For
instance, I badionotus has been reported in sandflats at densities of 1 individual per 7-8 m2.
ii) Pacific
A high diversity of sea cucumbers have been identified in the U.S. territories of Guam (30 species), CNMI,
and American Samoa, and in the U.S. Freely Associated States (28 species), including 16 of commercial
importance (Richmond, 1996). Fewer species occur in Hawaii. Most of the species that occur in the U.S.
Pacific territories overlap with those found throughout southeast Asia and the south Pacific.
The primary commercial species in the U.S. Pacific has been Actinopyga mauritiana, which inhabits the
surge zone of fringing and barrier reefs. It occurs to about 10 m depth, with the highest densities at about 2 m.
In Saipan, Northern Marianas, it is reported at densities of 1-6 animals per 100 m2 on the reef flat and 0.1-1.3/
100m2 on the reef slope. This species attains sexual maturity at about 22 cm, or 2-3 years in age, with a
lifespan of about 12 years.
B) Temperate
i) Northeastern Pacific
There are 14 species of sea cucumbers found in the Pacific northwest. Two of these are commercially
important, Parastichopus californicus (giant red sea cucumber) and P. parvimensis (warty sea cucumber).
They are both epibenthic detritivores (deposit feeders) that consume organic detritus and small organisms
within sediments and mud. These species are broadcast spawners, with separate sexes and a sex ratio of close
to 1:1. Spawning occurs in late spring and summer (May to August), typically in shallow water (<16 m); they
undergo visceral atrophy each year after spawning. Recruitment is sporadic and adults have a relatively high
natural mortality. The primary predators are the sea stars, Pycnopodia and Solaster. Because of their life
history traits, they are thought to have a low maximum yield per recruit and are particularly vulnerable to
overfishing (Rogers-Bennett and Ono, 2001).
Parastichopus californicus occurs from Baja California (Cedros Island) to the Gulf of Alaska, from the
lower intertidal to about 250 m. It is widely distributed throughout a variety of habitats (mud, gravel, rock
rubble and solid bedrock) and environments (exposed coastal areas to sheltered inlets), with the greatest
192
density in areas with accumulations of high organic sediments. Animals are slow growing (5-20 mm at 1 yr;
maximum size of 50 cm), and reach sexual maturity at 4-8 years; the lifespan is about 8-12 years (Cameron
and Frankboner, 1989).
Parastichopus parvimensis is most common from Baja California (Mexico) to Monterey Bay, California, but
occurs at lower abundances as far north as Point Conception. It is found from the intertidal to about 30 m
depth in areas with little water movement. This species is smaller than P. californicus, with a maximum length
of 30-40 cm.
A limited number of field surveys have been conducted to evaluate the status of P. californicus populations,
with information used to manage commercial fisheries. In California, these species have a patchy distribution
on rocky or sandy substrates, and do not appear to form seasonal, spawning or feeding aggregations. Population surveys have been monitored in the Channel Islands and Santa Barbara Islands since 1982. Between
1990-1994 the average density at all the monitored sites has declined but populations have been at about the
same levels as in the 1980s for the last several years. However, populations at fished sites were 50-80%
lower than at non-fished sites. For instance, at an established reserve in northern California (Cabrillo Reserve,
40-60 m) densities averaged around 1,000 per acre. Densities at a newly established reserve (Punta Gorda
Ecological Reserve) ranged from 120 to 350 per acre, with only the large size classes observed surveys
(Rogers-Bennett and Ono, 2001).
Oregon Department of Fish and Wildlife (ODFW) submersible surveys off southern Oregon found densities of
cucumbers of 0.1 - 0.22/m2 in 44 - 71 fathoms. Densities were less at shallower depths. Commercial densities
in British Columbia are estimated at less than 0.25/m2. However, at depths greater than 1300-1600 fathoms,
sea cucumbers are the most numerous animal found.
ii) North Atlantic
There are four species of sea cucumbers found off the Northwestern Atlantic. Only one of these, Cucumaria
frondosa (orange footed cucumber; pumpkins; great northern cucumber) is commercially important. C. frondosa
ranges throughout North Atlantic and Artic Oceans, including the Norwegian, Barents and North Sea and the
waters around Iceland. Its southern range along the northwestern Atlantic is Cape Cod and Nantucket,
Massachusetts. It is distributed from the intertidal to over 300 m depth, with the highest abundance from 3060 m. It inhabits a variety of substrates, including gravel, shell rocks, mud, with the densest populations found
in rocky areas.
This species is a suspension (filter) feeder, consuming phytoplankton and organic detritus. It is slow growing,
reaching a maximum size of 20 cm in inshore areas and 50 cm in deeper offshore waters. Sexes are separate
and animals reach sexual maturity at 2.5-3 years, when about 3.5 cm in length. Spawning occurs between
March and August. Animals grow to 12 cm within 5.5 years, and have an estimated lifespan of 10 years
(Chenoweth and McGowan, 2004).
In Maine, population densities can reach 5 individuals/m2 and populations can comprise up to 50% of the
benthic biomass. Dive surveys using transects demonstrate the patchy nature of the species, with abundances
ranging from 0.01 to 7.45 animals per square meter, with substantial differences in size and weight of animals
between sites.
193
2. Nature of sea cucumber fisheries
In the United States, sea cucumber fisheries can be separated into: 1) those occurring in state waters, each of
which is managed by individual states; and 2) those located in the EEZ (3-200 miles off the U.S. mainland and
surrounding Hawaii and the Caribbean and Pacific territories), which are managed by NOAA Fisheries in
coordination with Regional Fishery Management Councils.
There is no reported sea cucumber farming in the United States.
A) Tropical fisheries
i) Pacific
An intermittent fishery for holothurians in the Commonwealth of the Northern Marianas Islands (CNMI) dates
back to the 1930s, primarily for export to Japan. In 1941, total catch on Saipan was 54,284 kg. A small
commercial fishery for A. mauritiana and H. whitmaei was reopened for the first time in 1995, but was halted
in early 1997 due to declining CPUE (Trianni, 2003). From October 1995-May 1997 the total catch was
268,068 animals (76 metric tons), most from Saipan and Rota, primarily for export to Taiwan and Hong Kong.
One species (H. atra) is currently harvested on a subsistence level (Green, 1997).
In American Samoa, a small sea cucumber fishery targets the internal organs, which are bottled, fermented and
marketed locally as “sea”. The animals are returned after they eviscerate to allow for regeneration of the
organs. There are no official records of sea cucumber exports, although occasional exports are thought to
occur via foreign fishing vessels which visit American Samoa (T. Beeching, pers. Comm.).
In Guam, Stichopus horrens and Holothuria atra are harvested sporadically, at levels much less than in the
1800s, when catch of 2-3 tons were documented (Green, 1997). There is currently no active commercial
fishery, although certain public access areas experience subsistence collection by Micronesians.
In State waters of Hawaii a low amount of commercial harvest of sea cucumbers (“lole”) occurs (Table 1).
Table 1. Annual reported landings for the state of Hawaii. Source: Hawaii Division of Aquatic Resources
reported landings tables, 1984-2003. Available on line at http://wpacfin.nmfs.hawaii.edu/hi/dar/Pages/
hi_data_1.htm
Year
2003
2002
2001
2000
1999
1998
1997
1996
1995
1994
Landings
Total value (USD$)
130.6
$929
102.1
$699
54.0
$333
113.4
$811
51.3
$867
52.6
$920
50.3
$792
53.1
$534
23.1
$462
28.6
$443
Price per kg
$1.47
1.61
1.28
2.38
3.64
3.60
3.24
2.10
4.11
3.19
A Federal grant program funded a five-year project in several Pacific Islands [American Samoa, Guam, and
Federated States of Micronesia (FSM)] on resource surveys, aquaculture and management with emphasis on
three species, H. nobilis, A. mauritiana and H. atra. The project resulted in a general moratorium on export
194
harvests in Palau and portions of the FSM, and the development of a generic sea cucumber Management Plan
for Micronesian states (Richmond, 1996).
ii) Atlantic
Sea cucumbers (Holothuria spp.) are included in the fishery management unit (FMU) of the Fishery Management Plan for Corals and Reef Associated Plants and Invertebrates of Puerto Rico and the U.S. Virgin Islands.
However, there is no known harvest in federal waters of the U.S. Caribbean.
B) Temperate fisheries
Temperate North American sea cucumber fisheries are based on one or two species in each location.
Parastichopus californicus is the primary target on the west coast, with limited take of P. parvimensis, while
the east coast fishery is based on Cucumaria frondosa. According to FAO statistics, the total capture
fisheries production for the U.S. over the last 10 years (1992-2001) is 18,127 metric tons with a maximum
production of 4,583 mt in 2000 (Table 5).
i) California
The California fishery started in 1978 and is based on P. californicus and P. parvimensis. It is both a dive
and trawl fishery, with most trawling concentrated in southern California and diving in northern California. Until
1997 an average of 75% of the annual catch was from the southern California trawl fishery; this has declined in
recent years, partially due to prosecution of illegal trawl fishers which reduced the total number of trawl
fishermen. Beginning in 1997, divers who held sea urchin and abalone permits shifted their efforts to sea
cucumbers, and the dive fishery increased substantially, accounting for 80% of the total harvest (RogersBennett and Ono, 2001).
Annual landings remained under 40,000 kg until 1982, when the principal trawl areas shifted from Los Angeles
area ports to the Santa Barbara Channel. Annual landings fluctuated between about 20,000-60,000 kg until
1991 when it climbed to over 261,871 kg. In 1996, combined trawl and dive harvest peaked at 380,703 kg
with an ex-vessel value of USD $582,370 (Rogers-Bennett and Ono, 2001).
Since 1992-1993, a special permit has been required for sea cucumber harvest. Permit recipients must have
landed a minimum of 20 kg during the previous four year period. In 1997, separate permits were issued for
each gear type, with a limit on the total number of permits issued. There are currently 113 sea cucumber dive
permits and 36 trawl permits. There are no restrictions on catch.
ii) Oregon
Oregon’s sea cucumber fishery began in 1993 and is based on P. californicus, with most collection by hand
using dive gear. Harvest by trawl was also allowed, but it required an experimental gear permit (McCrae,
1994).
Oregon Department of Fish and Wildlife placed sea cucumbers within the Developmental Fisheries Program,
which was developed in 1993 to allow for the controlled development of new commercial fisheries. Under the
firs year of the program landings were 2335 kg by 9 divers, although 44 permits were issued; 4777 kg were
landed by 22 divers in 1994. Since this time very little harvest of sea cucumber has occurred in Oregon
waters, with exception of 1997 (Table 2). Permits were issued until 2003, when sea cucumbers were moved
to category B of the Developmental Fisheries Program species list, which include those species with less
potential for a viable fishery. For 2004, sea cucumber harvest no longer requires a developmental fishery
permit (McCrae, pers. Comm.).
195
Table 2. Kilograms of sea cucumbers landed and fishing effort in Oregon, 1995-2003.
1995 1996 1997 1998 1999 2000
2001
2002
2003
Kg landed
0
0 3295
0 3.28
132
15.9
0
312
Harvesters
5
2
1
2
2
Permits issued
15
3
7
9
2
7
8
4
2
iii)Washington
The Washington sea cucumber fishery is based one managed species, Parastichopus californicus. Commercial
harvest primarily involves the use of dive gear, with lower levels of harvest by an experimental trawl fishery.
Sea cucumbers may also be collected while diving for personal use, with a daily limit of 10 animals. There are
13 nonclassified sea cucumber species in Washington State waters that are collected at low levels for research
and aquariums under Washington Department of Fish and Wildlife (WDFW) Scientific Collecting permits.
The commercial dive fishery is open year round; the experimental trawl fishery is closed during soft-shell
Dungeness crab (reproductive) periods and trawling is prohibited in shrimp areas. The average statewide
CPUE has increased since 1996 and has reached a historic high, possibly as a result of a smaller, more efficient
fleet (Table 5). There are currently 46 licensed commercial divers, with a license reduction program initiated in
2002, with the goal of a reduction of the total number of licenses to 25.
Harvest in Washington State occurs under a cooperative management agreement with treaty tribes. There are
five management regions in Puget Sound, with about 50% of the total quota allocated for state harvest and
50% tribal harvest. The annual statewide harvest guideline (1997-2002) was 427,690 kg, with a total estimated
available commercial biomass of 5.58 million kg. The landed product has an ex-vessel value of about USD
$1.2 million. As a precautionary approach, the 2003-2004 quota has been reduced by 15% of that calculated
for 1997 until more recent biomass estimates are completed (Table 3). The quota has been developed determined
using the Schaefer (1954) surplus production model based on estimates of biomass from catch-effort data,
video surveys, and dive surveys (Bradbury, 1994).
Table 3. Harvest guidelines for sea cucumbers in Washington.
Source: Anonymous, 2003.
M anagement Region
San Juan
Strait of Juan de Fuca
C entral Puget Sound (26C)
C entral Puget Sound (rem aining areas)
Hood Canal
South Puget Sound
TOTA L
Harvestable
Surplus (kg)
295,372
70,755
17,280
906
3,084
30,840
372,055
Seven area closures for the dive fishery have been established in the current management plan, including two
that are closed for human health reasons. Regulations on the trawl fishery include spatial closures (no trawling
in water less than about 20 m depth), specific fishing locations, and restrictions on gear type and size, including
maximum beam width for beam trawl gear and minimum mesh size for otter trawl gear.
Fish receiving tickets are submitted to WDFW after each fishing trip for use in determining when the annual
tribal and State commercial harvest quota is reached. Fishermen also submit monthly harvest logs that include
the date, vessel name or boat registration number, location fished, pounds landed, average depth of harvest,
number of divers, and total diver hours spent fishing.
196
iv) Alaska
The Alaska sea cucumber fishery for P. californicus began in 1981 in Southeast Alaska as an experimental
fishery, and in 1987 around Kodiak Island. Sea cucumbers are collected by hand using dive gear, typically at
depths of 3-20 m, with no restrictions on the use of mixed gases or saturation diving. Initially most vessels
were small skiffs operating as a day fishery. More recently, larger vessels with two divers and a crewman and
living quarters have extended the range and duration of fishing trips.
The dive fishery in both locations was initially based only on a permit system. However, due to rapid expansion,
the fishery exceeded the ability of the Alaska Department of Fish and Game to manage by a permit system. The
fishery was closed in May 1990, until a management plan was written. This plan relies on a quota developed
based on historic production, fisheries performance and biannual survey data of population biomass with a
total harvest rate of 6%. The harvest rate is estimated to be 50% of MSY, calculated using surplus production
model that incorporates 1) an estimate of virgin population size; 2) a reduction of the quota to 50% of the
harvest rate derived from the model; and 3) with another 30% reduction to account for field sampling variability.
In addition, there is no allowable harvest in areas with biomass estimates below a threshold of 1kg/m of
shoreline (Woodby, Kruse and Larson, 1993).
The Southeast Alaska Sea Cucumber Commercial Fisheries Management plan was completed in October
1990. The management plan established 18 areas closed to fishing and annual guideline harvest levels of 6.4%
of the total sea cucumber biomass taken on a 3 year rotational basis. There is also a seasonal closure (AprilSeptember), and a limit on the number of fishing days and hours per week, and trip limits for each vessel.
There a progressive increase in effort to a maximum of 424 divers in 1995-1996 season. Beginning in 1996,
a moratorium on the dive fishery was imposed, limiting the number of divers able to participate in the fishery to
472. There were 235 permits issued for the 2001/2002 season (Hebert and Pritchett, 2002). The quota for
2001/2002 was 646,466 kg, with an actual harvest of 652,477 kg with an estimated ex-vessel value of USD
$2,517,289 (Table 4b). For the 2002/2003 an additional 58,000 kg were added to the quota within three new
collection areas.
The commercial fishery was reopened in Kodiak in 1991 under a new management plan. Current management
measures include 1) a closed season from May through September to protect spawning aggregations; and 2)
fifteen large harvest refugia within the managed area. In addition, sea cucumber research control sites are
monitored annually to differentiate environmental effects from fishing effects. Since 1995, fishing periods have
also been reduced to three days per week to allow analysis of fishing performance and monitor progress
towards the established harvest guidelines (Ruccio and Jackson, 2002). Divers are licensed and must obtain a
Commercial Fisheries Entry Commission interim use permit. Fish tickets are required from fishermen, operators
of commercial fishing vessels, processors and buyers. In addition, completed logbooks that provide coordinates
of fishing areas must be submitted by each fishing vessel as one component of each fish ticket (Ruccio and
Jackson, 2002). The number of permits has ranged from 18-86 each year, with a maximum number issued in
1986 and 18 permits issued in 2001. Annual quotas have been established for each area as guideline levels of
harvest, currently amounting to 113,759 kg divided among Kodiak (90,719 kg) and Chignick (23,040 kg).
Harvest in the 2000/2001 season amounted to 69,216 kg . Prices have fluctuated between USD $0.42-0.68
per kg with a total landed value in 2001 of about USD $190,000. Starting in 2002/2003 season, an additional
four areas in Kodiak district and three other areas in the Aleutian Islands were open to experimental fisheries,
with a guideline harvest level of 2268 kg for each area (Ruccio and Jackson, 2002).
197
Table 4a. Thousands of kilograms of sea cucumbers landed, fishing effort and landed
value for Kodiak Island in Alaska, 1993-2001.
1993 1994 1995 1996 1997 1998
1999
2000 2001
Kg landed
256.1 187.6 65.8 73.7
60 64.6
52.7
52.7
69.2
No landings
487
269
60
93
65
55
36
56
73
Permits issued
50
86
21
31
26
16
19
20
18
Value/kg (USD)
0.42 0.54 0.57 0.57 0.53 0.54
0.54
0.68
0.57
Table 4b. Total landings of sea cucumbers (thousands of kg), number of divers and exvessel value in millions of USD from 1986-2001 in Southeast Alaska.
Year
1986
1987
1988
1989
1990
1991
1992
1993
1994
1995
1996
1997
1998
1999
2000
2001
Kg landed
15.44
29.51
363.51
1051.58
364.78
394.62
566.82
437.42
599.75
604.23
411.32
405.85
478.80
711.98
525.44
652.48
No divers
7
11
57
205
143
187
240
320
261
424
294
226
219
200
220
235
Ex-vessel Value
0.007
0.014
0.169
0.969
0.472
0.697
0.988
0.995
2.361
1.846
1.169
1.458
1.636
3.060
2.583
2.517
v) Maine
The Maine sea cucumber fishery is a low value/high volume fishery that targets C. frondosa. The fishery began
in 1988 with one operator, and expanded in 1994 when Asian markets for this species emerged. Fishermen
use boats ranging from 12-30 m in length equipped with either scallop chain sweeps or light urchin drag gear.
The gear is limited to 167 cm width and 7 m length and has a head bail constructed of less than 3.8 cm round
steel stock. On a typical day, each boat harvests 70-200 totes of sea cucumbers. Catch per boat per day was
about 7,212 kg, with an average of 16 (+/-5) tows per day. There are currently 16 endorsements, although
only three are active (Feindel, 2002).
In the mid 1990s, the industry employed from 75-100 individuals that processed sea cucumbers and 15-20
fishermen, with annual harvest of 453,542-1,360,512 kg. Landings had increased to over 3.6 million kg in
1999 and over 4.08 million kg in 2000. In 2001, landings decreased to 1.27 million kg. The decline was
associated with the closure of two of the three processing plants (Feindel, 2002).
There have been some problems associated with the fishery. The primary concern is that most of the fishing
effort is clumped in a few sites in three locations in eastern Maine, and there are anecdotal reports that some
sites have been fished out. In some areas there are substantial amounts of bycatch associated with the fishery.
198
In general, bycatch is low in rocky areas where the species forms dense aggregations, while bycatch is much
higher in muddy and gravel environments (Feindel, 2002).
To address concerns of possible depletion of the resource as interest in the fishery peaked, and to address gear
conflict issues among lobster fisheries, regulations were implemented in March 2000 under the 1999 Sustainable
Development of Emerging Fisheries Act. This included restrictions that limited the fishing season (closures
between July 1 and Sept 31), defined gear size, and established a maximum number of endorsements, with
licenses given only to individuals that had sold 100,000 kg during the previous year. Licensed fishermen are
required to submit logbooks that include information on catch, time at sea, area fished and the value (Feindel,
2002). Maine has established a small (USD$500) Sea Cucumber Management Fund (§6813) to research and
manage the State’s sea cucumber fishery and enforce laws related to sea cucumbers.
3. Domestic and international trade
A. Exports and domestic consumption
Most of the Parastichopus spp. harvested in Alaska, California, Oregon and Washington are exported to
Hong Kong, Chinese Taipei, mainland China and Korea. Chinese markets within the United States also
purchase a portion of the sea cucumber catch. The majority are boiled, dried and salted before export, while
lesser quantities are marketed as a frozen, pickled or live product. Exports of Parastichopus spp. are worth
0.31-0.68/kg. while the processed sea cucumbers can sell for up to $9 per kg (wholesale).
In Maine, fishermen are paid about USD $0.05 per unprocessed animal ($7 per tote) of C. frondosa. Internal
muscle bands and the dried body wall are the primary export product, currently worth about $1.59 per kg.
After harvest the animals are either loaded onto refrigerated trucks at the dock and shipped to Seattle for
processing, or they are processed in Maine and shipped to mainland China, Hong Kong, South Korea, Singapore,
Chinese Taipei and Japan. The peak export value of this fishery is estimated to be less than 1% of the global
trade (Feindel, 2002).
The byproduct of processing from C. frondosa is marketed in the United States as nutritional supplement
providing chondroiton (NutriSea), and is also sold as a treatment for arthritis for people (ArthriSea and
SeaCuMAX) and pets (Sea Jerky) (Coast side Bio Resources, Stonington, Maine). The by product is also
marketed as compost in Maine.
In American Samoa, the viscera of sea cucumbers are bottled, fermented and sold locally as a product called
“sea”.
B. Imports
i) Beche-de-mer
No commercial statistics are available on U.S. sea cucumber imports for food.
The west coast of the U.S. is a trans-shipment point for sea cucumbers originating in Latin America en route to
Asia.
199
ii) Aquarium trade
The United States imports a small volume of live sea cucumbers for the aquarium trade primarily from southeast Asia. The genus Pseudocolochirus is the dominant import, although several smaller species such as
Pentacta anceps and Colochirus robustus are also available. One Caribbean species, I. badionatus, is
commonly imported and also collected in U.S. waters
.
In Washington state, imports of live sea cucumbers is prohibited except by permit for scientific research or
display under WDFW invertebrate disease control permits. There are no restrictions on import of market
ready species for human consumption.
Table 5. Sea cucumber production and export. Production is in metric tons (FAO
FishStat Plus v. 2.3; Hong Kong SAR import statistics).
U.S.
Production
Hong Kong
imports
1991 1992 1993 1994 1995 1996 1997 1998 1999
<0.5 481 472 2141 729 1779
- 2406 3732
2000
4583
181.57
Table 6. Summary of available information on commercial landings of sea cucumbers in
the United States in metric tons (mt), live weight. * Washington data for 1999-2001 is
the total allowable quota (not landings).
Alaska
Oregon
California
1993
1994
693.5
786.7
670
2.3
4.8
265.8
293.0
Washington
Maine
1451
1995
1996
1997
1998
1999
485
465.8
543.4
764.6
578
721.7
0
0
2.9
0
0.003
0.1
0.01
267.6
381
193.0
341
272
529
237
227.0
208
427*
427*
427*
1950
1270
453.0
2359
3630
4080
1270
200
2000
2001
Table 7. Controls and enforcement measures for sea cucumber fisheries in U.S. temperate
waters.
Location
Alaska, USA
Licensing
Divers
registered and
permitted.
Washington,
USA
Limited entry;
190 divers in
2000.
Oregon, USA
Licenses issued
up to 2003,
with only two
divers
requesting a
license.
California,
USA
Separate annual
permits for
each gear type:
113 dive
permits and 36
sea cucumber
trawl permits.
16
endorcements
(only 3 active).
Maine, USA
Reporting
Dive/harvest
logbook with
date, location
(GPS), depth,
bottom time,
quantity.
Logbooks with
daily reporting
of catch to
avoid
exceeding
quota.
Fish receiving
tickets (dock
ticket) required
from sea
cucumber
dealers with
fishermen’s
name, location,
date and
amount.
Dive and trawl
fisheries target
different
species; all data
lumped as sea
cucumber
landings.
Harvester
Logbooks.
201
Validation
Divers can only obtain permits
for urchins or sea cucumbers but
not both.
Must submit logbooks every
month with data on date, depth
location and amount (number
and weight) collected.
Cucumbers are listed under
developmental fisheries species
list category B. As of 2004 the
fishery no longer requires a
permit.
Limit permits by requiring a
minimum landing of 50 lbs
during the previous year. Trawl
fishery declined in 1998-1999
due to prosecution of 16 trawl
fishermen that fraudulently
obtained sea cucumber permits.
Limit licenses to fishermen that
landed >250,000 lbs in a
previous year. No incidental
take allowed, only take through
targeted, licensed fishery.
Literature Cited
Alaska Department of Fish and Game, 1990.
Anonymous, 2003. Sea cucumber harvest management plan 2003-2004 for commercial fisheries conducted
by U.S. v. Washington Subproceeding 89-3 Treaty Tribes and the state of Washington. 14 pp.
Bradbury, A. 1994. Sea cucumber dive fishery in Washington State. Beche-De-Mer Information Bulletin,
SPC 6: 15-16.
Cameron, J. L. and P. V. Frankboner. 1989. Reproductive biology of the commercial sea cucumber
Parastichopus californicus (Stimpson)(Echinodermata: Holothuroidea). II. Observations on the ecology
of development, recruitment, and the juvenile life stage. Journal of Experimental Marine Biology and
Ecology. 127:43-67.
Chenoweth, S. and J McGowan 2004. Sea Cucumbers in Maine: Fishery and Biology. Maine Department of
Marine Resources. http://www.state.me.us/dmr/publications/seacucumbers.html
Feindel, S. 2002. Status of the Maine Sea Cuucmber (Cucumaria frondosa) Fishery. Submitted to Standing
Legislative Committee on Marine Resources. Department of Marine Resources, . 35 pp.
Green, A. 1997. An assessment of the status of the coral reef resources, and their patterns of use, in the U.S.
Pacific Islands. A report to NOAA award no. NA67AC0940. 278 pp.
Hebert, K and M Pritchett. 2002 Report to the board of fisheries, miscellaneous dive fisheries. Regional
Information report No IJ02-45. Alaska Department of Fish and Game, Division of Commercial Fisheries,
Juneau Alaska. 10.1-10.30.
McCrae, J. 1994. Oregon Developmental Species. Sea cucumbers Parastichopus sp. Oregon Dept. of Fish
and Wildlife
Richmond, R.H. 1996. Suggestions for the management of sea cucumber resources in Micronesia. Results of
the workshop “A Regional Management Plan for A Sustainable Sea Cucumber Fishery for Micronesia.
Technical Report 101. University of Guam Marine Laboratory. 68 pp.
Rogers-Bennett and D.S. Ono. 2001. Sea cucumbers. In: California Living Marine Resources: a status report.
California Department of Fish and Game. pp 131-134.
Ruccio, M.P. and D.R. Jackson, 2002. Red sea cucumber and green sea urchin commercial fisheries management
plans for the registration area J (westward region), 2002/03. Regional Information Report No. 4K02-44.
Alaska Department of Fish and Game Division of Commercial Fisheries. 14 pp.
Schroeter, S.C., D. Reed, D. Kusher, J. Estes and D.S. Ono. 2001.The use of marine reserves for fishery
independent monitoring: a case study for the warty sea cucumber, Parastichopus parvimensis.
Trianni, M.S. 2002. Summary of data collected from the sea cucumber fishery on Rota, Commonwealth of the
Northern Mariana Islands. Beche-De-Mer Information Bulletin, SPC 16:5-11.
Trianni, M. S. 2003. Evaluation of the resource following the sea cucumber fishery of Saipan, Northern Mariana
Islands. Proc. 9th Intl Coral reef Symp. 2:829-834.
Woodby, DA, GH Kruse and RC Larson, 1993. A conservative application of a surplus production model to
the sea cucumber fishery in southeast Alaska. Proceedings of the International Symposium on Management
for Exploited Fish Populations. Alaska Sea Grant. pp. 191-202.
202
NATIONAL REPORT – CANADA
Philip Lambert
Royal British Columbia Museum, Canada
1. Nature of sea cuucumber fisheries
a. Species harvested
Species: Parastichopus californicus (Stichopodidae)
Location: British Columbia, west coast of Canada.
Range of species: Gulf of Alaska to Baja California; 0-249m.
Species: Cucumaria frondosa (Cucumariidae)
Location: Newfoundland, east coast of Canada. Test fishery. Most from by-catch of scallop dragging.
b. History of fishery
•
•
•
•
•
•
•
Commercial exploitation began in 1971.
Licensed fishery began in 1980 with many quotas overruns.
Area closures and adjusted quotas began in 1986.
Licenses limited in 1991.
1993-1996 a 3 year rotation introduced.
In 1995 individual quota system introduced. Rotation no longer used.
Quota management areas are being broken into smaller parcels to distribute effort.
c. Status of fishery in British Columbia
•
•
•
•
•
Total allowable catch (TAC) based on stock assessment research earlier in the year. Commercial
license holders and First Nations participate in biomass surveys.
TAC in 2000 816,000 lbs
TAC in 2001 850,000 lbs
25% of BC coast is open for commercial harvesting, 25% for research, 50% closed to harvesting
pending more basic biological information and a review of adaptive management plan.
80% of fishery is on north and central coast of BC; 20% south coast.
d. Harvesting
•
•
•
•
Harvested by divers.
3 to 4 week fishery in the fall of year.
Product sold as frozen muscle strips and dried skin.
Exported to Hong Kong, Taiwan, mainland China, and Korea plus some domestic market.
203
e. Value of sea cucumbers in British Columbia
In 2002:
• 1,200 tonnes were harvested.
• Landed value was 1.5 million CAN$
• Wholesale value was 6.5 million CAN$
• Recreational harvesters are allowed 12 per day with a possession limit of 24.
Landed Value
Wholesale Value
7.0
2.5
6.0
5.0
Millions $CAN
Millions of $CAN
2.0
1.5
1.0
4.0
3.0
2.0
0.5
1.0
0.0
0.0
1995 1996 1997 1998 1999 2000 2001 2002
1995 1996 1997 1998 1999 2000 2001 2002
YEAR
YEAR
f. National Policy
•
•
•
•
•
Federal Department of Fisheries and Oceans manages the fishery through an adaptive management
strategy.
Sea cucumber Sectoral committee meets twice a year to discuss research objectives and plans, review
stock assessment advice, and draft a management plan.
85 licenses based on an individual quota system.
Minimum 2% of TAC goes to First Nations food, social and ceremonial use. The rest is distributed to
the commercial licenses.
The fishers are required to develop and fund a catch monitoring and validation program to ensure area
and individual quotas are not exceeded.
g. Outlook
•
•
•
With over 50% of the coast closed to harvesting there is presently no risk of stock collapse.
Annual quotas are closely adhered to through the port validation of all landings.
The effort or removing these detritus feeders from the ecosystem has not been investigated.
204
NATIONAL REPORT – EGYPT
AJ Lawrence1, M Ahmed, M Hanafy, H Gabr, A Ibrahim, and AA-FA Gab-Alla
1
Department of Biological Sciences, University of Hull, United Kingdom
1. Nature of sea cucumber fisheries
First noted in the mid-1990s, the sea cucumber fishery started officially in 1998 in the southern part of Egypt.
In the Red Sea the harvesting of sea cucumber involves two processes. In the south and in the Gulf of Suez
trawlers harvest the sea cucumber using a benthic trawl. Initially part of the bi-catch, sea cucumber were later
specifically targeted and subject to heavy trawling activity. In the central part of the Red Sea and the Gulf of
Aqaba, scuba-diving is used for collecting the animals. In addition, some species are harvested by hand at low
tide on the reef flats. In Egypt the processing of sea cucumber is not significantly different from the methods
described previously in other fisheries and many descriptions have been given.
The catch and the total income derived from Bech-de-mer fishing in the Red Sea is known to have increased
significantly between 1998 and 2000, mainly due to the dramatic increase in the value of sea cucumber over
that period. In 1999, as the price of Bech-de-mer increased, the fishery expanded to cover the rest of the
Egyptian coast of the Red Sea. During this time the number of boats using either SCUBA or trawling techniques
doubled and the number of companies involved in the fishery increased significantly.
In April 2000 the Red Sea Governorate banned the fishing of sea cucumber in the Red Sea until a stock
assessment supported by the Darwin Initiative could be performed. However, this ban only existed for the area
of coastline under the jurisdiction of the Red Sea Governorate. The neighboring Suez Governorate, for example,
continued with an open fishery. This lead to further depletion of stocks in the Red Sea as a whole, and added
to the difficulty of policing of Red Sea Governorate coastal areas.
Furthermore, the ban also resulted in the development of a large illegal fishery in the region under the jurisdiction
of the Red Sea Governorate. This illegal fishery continued unabated both as a result of the low level of patrolling
(and difficulty of policing such a large area) and the development of a conflict between the EEAA, which
wanted to limit the fishery, and the Ministry of Agriculture, Department of Fisheries, which aimed to exploit the
resource to its maximum. There was a further, social, consequence of the illegal fishery. The official number of
recorded deaths of fishermen involved in fishing for sea cucumber using SCUBA increased six-fold between
2000-2002.
Further evidence of the likely over-exploitation of the commercial species of sea cucumber in Egypt was
illustrated by the fact that during the period 1998-2002 the number of species fished increased from an initial
two, to up to 14 in the case of SCUBA. Thus, as the fishery increased, the numbers of the most valued species
decreased and fishermen attempted to compensate for this by collecting other, less valuable species.
205
As a result of the conflict between different government agencies, the sea cucumber fishery was re-opened in
2002 and licenses were given to fishermen to collect sea cucumber. A total number of 52 boat licenses and 100
individual fishermen licenses were issued. Due to the further depletion of commercial holothuria, in March
2003 a meeting was held in the Red Sea Governorate to discuss the problem of seacucumber fishing in the Red
Sea. The meeting included representatives from the EEAA, Ministry of Agriculture and Red Sea Governor. As
a result of this meeting a second, complete ban on the fishery was instigated until the report of the current stock
assessment could be provided.
Clear differences have been found in the abundance of the main commercial species when fished and nonfished areas are compared. There has been an almost complete loss of the most valuable species H. scabra
and H. nobilis, as well as the removal of most commercial species from most fished areas. Whilst both
seagrass and coral sites have been targeted by fishermen, their impact on seagrass areas appears to have been
more severe.
Based on the interview data it is estimated that approximately 2400 tonnes of H. scabra were collected by
trawling in 1998, dropping to 48 tonnes by 2001. Collection of H. scabra by divers peaked in 2001 with 896
tonnes and fell in 2002 to 67 tonnes. These figures are masked partly by the collection of other species, most
of which have also shown a marked decline in catch. Based on the area survey it is estimated that there is
approximately 400 tonnes of H. scabra left throughout the Red Sea coast of Egypt. This figure takes no
account of habitat selectivity by this or any other species.
206
NATIONAL REPORT – AUSTRALIA
The CITES Management Authority of Australia
The Australian Government Department of the Environment and Heritage (DEH)]
Sea cucumber fisheries and current trade
- Legal trade
The Department of the Environment and Heritage (DEH), the CITES Management Authority of Australia, is
responsible for the implementation of Australia’s environmental legislation, the Environment Protection and
Biodiversity Conservation Act 1999 (EPBC Act). The international movement of wildlife specimens is regulated
under Part 13A of the EPBC Act, the objectives of which are:
•
•
•
•
•
•
•
To ensure that Australia complies with its obligations under CITES and the Biodiversity Convention;
To protect wildlife that may be adversely affected by trade;
To promote the conservation of biodiversity in Australia and other countries;
To ensure that any commercial utilisation of Australian native wildlife for the purposes of export is
managed in an ecologically sustainable way;
To promote humane treatment of wildlife;
To ensure ethical conduct during any research associated with the utilisation of wildlife; and
To ensure that the precautionary principle is taken into account in making decisions relating to the
utilisation of wildlife.
Exporting
Sea cucumbers are considered regulated native specimens under Part 13A of the EPBC Act and therefore
require an export permit from DEH. In order to get this permit, the operation from which the specimens are
sourced needs to be an approved wildlife trade operation under the EPBC Act. There are a number of
requirements that need to be met in order for an operation to be approved under the EPBC Act, including
meeting the objectives of the Part (as listed above) and a 20 business day public comment period. Permits may
also be issued for non-commercial purposes including education and research. Further detail regarding
requirements for an approved operation under the EPBC Act can be found at http://www.deh.gov.au/coasts/
fisheries/index.html .
Currently six sea cucumber fisheries in Australia have export approval under the EPBC Act (see Table 1 for
details). A number of permits have been issued to companies to export sea cucumber product from these
fisheries. These fisheries will all be undergoing a comprehensive assessment of their ecologically sustainable
management against the Guidelines for the Ecologically Sustainable Management of Fisheries (http://
www.deh.gov.au/coasts/fisheries/assessment/guidelines.html) within the next year.
Importing
No conservation-based import controls currently exist for non-live sea-cucumbers (controls may exist for
other purposes such as animal or human health quarantine). For live sea-cucumbers, some species may be
imported under an import permit; the remainder may not be imported.
- Illegal, unreported and unregulated trade
No data is available on levels of illegal, unreported and unregulated export or import.
207
- Bycatch
A very minor amount of sea cucumber is taken as bycatch in a number of trawl fisheries around Australia. For
further detail on fisheries that have reported sea cucumber bycatch please see Table 1. Sea cucumber is not
permitted to be retained if taken as bycatch in any of these fisheries.
- Socio economic characteristics of the trade is sea cucumbers
No information is available on the socio-economic characteristics of Australian trade in sea cucumbers.
Management and conservation strategies and practices
-
Fisheries management approaches
-
Wild harvest
-
Aquaculture
-
Restocking
Information relating to these items can be found in Table 1.
Australian sea cucumber fisheries are separately managed by the Commonwealth and State fisheries management
authorities, therefore management arrangements vary across the different Australian jurisdictions.
208
Table 1 Summary of Australian sea cucumber fisheries
Commonwealth
M anagement
agency
Fishery
Total Catch
2002-2003
Status
Species
harvested
Management
measures
Other
information
-
Australian Fisheries M anagement Authority
Coral Sea Fishery (holothurian component)
10,042kg were taken during the financial year. Almost no fishing has taken
place since then.
Unknown.
Actinopyga mauritiana (Surf redfish)
Actinopyga miliaris (Blackfish)
Holothuria atra (Lollyfish)
Holothuria nobilis (W hite teatfish)
Holothuria scabra (Sandfish)
Holothuria whitmaei (Black teatfish)
Stichopus chloronatus (Greenfish)
Thelenota ananas (Prickly redfish)
Thelenota anax (Amberfish)
• Harvest not permitted within Nature Reserves within the fishery boundaries.
• Sea cucumber may only be collected by hand with the use of SCUBA
diving equipment.
• Number of persons in the fishing operation limited to seven.
• Catch limit of 75 t landed weight, per permit per year.
• Species specific minimum size limit guidelines.
• Catch limits for high value species per permit, comprising:
- W hite teatfish – 2 tonnes
- Black teatfish – 500 kg
- Prickly redfish – 10 tonnes
- Sandfish – 5 tonnes
- Surf redfish – 5 tonnes
- All other species – Uncaught proportion of 75 tonnes.
Two permits have been granted for the sea cucumber sector of the Coral Sea
Fishery.
Fishery
Total Catch
2002
Torres Strait Sea Cucumber Fishery
Queensland logbooks recorded 126,556kg
Status
Species
harvested
Sandfish, black teatfish and surf redfish overfished.
Actinopyga echinites (Deepwater redfish)
Actinopyga lecanora (Stonefish)
Actinopyga mauritiana (Surf redfish)
Actinopyga miliaris (Blackfish)
Bohadschia vitiensis (Brown sandfish)
Holothuria atra (Lollyfish)
Holothuria edulis (Pinkfish)
Holothuria fuscopunctata (Elephant’s trunkfish)
Holothuria nobilis (W hite teatfish)
Holothuria scabra (Sandfish)
Holothuria whitmaei (Black teatfish)
Stichopus chloronatus (Greenfish)
Stichopus variegates (Curry fish)
Thelenota ananas (Prickly redfish)
Thelenota anax (Amberfish)
209
Management
measures
Other
information
•
Limiting the method of taking sea cucumber to either hand or hand held nonmechanical implement, without underwater breathing apparatus.
•
A ban on the use of hookah gear.
•
Limiting Islander dinghies to less than 7 metres in length.
•
Non-Islander boat limited to 20 metres.
•
Size limits.
•
Bag limits for traditional fishing.
•
Total Allowable Catch (TAC) of:
- Sandfish – 0 tonnes
- Black teatfish – 0 tonnes
- Surf redfish – 0 tonnes
- White teatfish 260 tonnes
- Prickly redfish – 260 tonnes
- All other sea cucumber – collectively 80 tonnes
Fishing is limited to traditional inhabitants with the exception of one long-term
non-Islander operator. Additional restrictions apply to this license holder to
promote participation of Islanders in these activities. There are approximately 180
Islander dinghies in the fishery.
Fishing for sea cucumber became important to the economy in the Torres Strait in
the early 18th century. The fishery has been through periods of expansion and
contraction primarily as a result of changes in market demand. During the 1990s,
the fishery in Torres Strait experienced a resurgence.
Fishing for sandfish on the Papua New Guinea side of Torres Strait was closed in
1993 due to concerns about overfishing. The closure remained in force until
October 1995 and the fishery then operated under a management plan which
included a 40 t (dry wt)/year Total Allowable Catch, a closed season and minimum
sizes. Following a few years of fishing the sandfish fishery on Warrior Reef was
again closed. Fishery independent assessments of the reef conducted since the
closure have shown very little, if any signs of recovery.
The sea cucumber fishery on the Australian side of Torres Strait experienced a
similar boom which began in 1994, with catches in 1995 estimated to be between
1200 t and 1400 t; all but ~50 t of this being sandfish. Levels of exploitation were
similar to those prior to the closure of the PNG Torres Strait fishery, and a survey
in November 1995 found that the fishery was probably over exploited.
A zero TAC has been placed on three species in response to concerns about
sustainability of the species.
Recreational
harvest
Illegal harvest
Bycatch
Re-stocking /
Aquaculture
None
There are some reports of illegal harvesting of sea cucumber by Papua New
Guinean fishermen. Quantities taken are unknown.
Sea cucumber are taken as bycatch in the Northern Prawn Fishery and Torres Strait
Prawn Fishery, but are not retained.
None currently
210
Table 1 Summary of Australian sea cucumber fisheries (continued)
Queensland
Management
agency
Fishery
Total Catch
2002/2003
Status
Species
harvested
Management
measures
Other
information
Queensland Fisheries Service
Queensland East Coast Beche-de-mer Fishery
264 tonnes (wet gutted weight)
Black teatfish overfished.
Actinopyga echinites (Deepwater redfish)
Actinopyga mauritiana (Surf redfish)
Actinopyga miliaris (Blackfish)
Holothuria atra (Lollyfish)
Holothuria fuscopunctata (Elephant’s trunkfish)
Holothuria nobilis (White teatfish)
Holothuria scabra (Sandfish)
Holothuria scabra var. versicolor (Golden sandfish)
Holothuria whitmaei (Black teatfish)
Stichopus chloronatus (Greenfish)
Stichopus variegates (Curry fish)
Thelenota ananas (Prickly redfish)
•
Limited entry.
•
Minimum size limit of 15 cm for all species.
•
Specimens may only be taken by hand, and commercial
fishers may use underwater breathing apparatus
•
TAC of 380 tonnes (wet weight) comprising:
- Black teatfish – 0 tonnes
- White teatfish – 127 tonnes
- All other sea cucumber – 253 tonnes
•
TAC is divided among the 18 authority holders using a
system of individual quotas.
•
Zones associated with Marine Parks closed to beche-de-mer
harvest.
•
Permanent closure at the southern end of the fishery.
•
Only 4 dories may be used in association with the primary
fishing vessel.
•
Prior reporting of product landings
Access to black teatfish populations in the Queensland East Coast
Fishery was closed in October 1999 in response to serious decline
in abundance of the species. Since this time fishery independent
assessments of black teatfish stocks have shown very little, if any
signs of recovery.
211
Queensland (continued)
Fishery
Total Catch
2003
Status
Species
harvested
Management
measures
Other
information
Fishery
Recreational
harvest
Bycatch
Re-stocking /
Aquaculture
Queensland Morton Bay Beche-de-mer Fishery
24 tonnes sandfish (wet gutted weight )
Developmental fishery – underfished.
Holothuria scabra (Sandfish)
Stichopus horrens (Peanutfish)
•
Limited entry.
•
Minimum size limit of 17 cm for both species.
•
Specimens may only be taken by hand. Hookah and scuba
equipment is not permitted.
•
Fishery closed between 1 October and 30 November each year.
•
TAC of 45 tonnes gutted wet weight of sandfish and 25 tonnes
gutted wet weight of peanutfish each year.
•
Zonal trigger limits for tonnage collected and time fished.
•
No more than two boats (less than 7m in length), each with no
more than 3 persons, may be used at any one time.
•
Prior reporting of fishing activity
Only one non-transferable authority has been issued for the fishery.
The fishery commenced harvesting in April 2003.
There are small amounts of colourful holothurians collected in the
Queensland Marine Aquarium Fishery for ornamental aquarium
purposes.
Unknown, however thought to be very low.
Sea cucumber taken as very minor bycatch in prawn trawl fishery.
They are not able to be retained.
One licensed hatchery (sandfish) and arrangements being made for
trial growout.
212
Table 1 Summary of Australian sea cucumber fisheries (continued)
Western Australia
Management
agency
Fishery
Total Catch
2001/02
Status
Species
harvested
Management
measures
Other
information
Department of Fisheries, Western Australia
West Australian Beche-de-mer Fishery
71,360 kg (live weight)
Developmental fishery
Actinopyga echinites (Deep water red fish)
Holothuria atra (Lolly fish)
Holothuria fuscogilva (White teatfish)
Holothuria nobilis (Black teatfish)
Holothuria scabra (Sandfish)
Thelenota ananas (Prickly red fish)
•
Limited entry.
•
Specimens can only be harvested by diving or direct
collection by hand.
•
Species specific size limits.
•
Limited species permitted to be collected.
•
Maximum of 4 divers at any one time.
Access to the fishery is limited to six endorsed operators, all
owned by the same company. There is one Aboriginal community
with a non-transferable permit but it is not currently active.
Since the rapid development of the fishery in the mid 1990’s,
when catch rates reflected the ‘virgin’ nature of the stock,
production from the fishery has begun to stabilise. Fishing occurs
in a relatively limited area compared to the wide distribution of the
species within Western Australia.
Sandfish dominates harvest from the fishery.
Recreational
harvest
Bycatch
Re-stocking /
Aquaculture
Negligible
Sea cucumber taken as bycatch in trawling fisheries but they are
not allowed to retain it.
No established activity.
213
Northern Territory
Management
agency
Fishery
Total Catch
2002
Status
Species
harvested
Management
measures
Other
information
Northern Territory Department of Business, Industry and Resource
Development (DBIRD)
Northern Territory Trepang Fishery
207 tonnes
Ecologically sustainable. Low participants (only 6 operators), large area.
Actinopyga echinites (Deep water red fish)
Holothuria atra (Lolly fish)
Holothuria nobilis (Black teatfish)
Holothuria scabra (Sandfish)
Thelenota ananas (Prickly red fish)
•
Limited entry.
•
Specimens can only be harvested by hand.
•
Species specific size limits.
•
Fishery split into two zones, with no more than three licences in
each.
Entry is limited to six licences, and all are owned by a single company.
The functional fishery only utilises a small proportion of the available
fishing grounds. Sandfish dominates harvest from the fishery.
The DBIRD advises that the NT Trepang (sea cucumber) fishery is a well
managed sustainable fishery. The fishery is still in the developmental
stage with catches well below the long term historical catch rates from
periods when the fishery was heavily fished. The management
arrangements aim to reduce any uncertainties by limiting the total number
of licences available, fishing capacity, permitted methods and protecting
adequate numbers of breeding stock. The adoption of such a strategy aims
to ensure there is a high probability of the fishery not exceeding
sustainable harvest levels, acknowledging that historical limits were a
significant magnitude higher than current catch.
Recreational
harvest
Bycatch
Negligible
Re-stocking /
Aquaculture
Great interest in stocking and ranching for aquaculture in regional and
indigenous communities.
Nil
214
NATIONAL REPORT – COSTA RICA
1. Information on wild populations
a) Species of non-commercial and commercial sea cucumbers in your country's waters:
Commercial: Holothuria inornata y Stichopus fuscus
Non-commercial: There is no information
b) Area of distribution, and habitats if known:
Distribution: In Costa Rica there are cucumbers of sea on both coasts: Pacific and Caribbean.It is known
that there are cucumbers in the zones of sand, rocks, coral reef, to little depth, in clear and not contaminated waters.
American Pacific: In Costa Rica: Bay Salinas, Bay Cuajiniquil, Bay Santa Elena, Bay Culebra (Snake)
(according to study realized in the place).
Habitat: superficial Waters in botton sandy, rocky (preferred).
c) Abundance (including anecdotal information): There is no information.
2. Nature of sea cucumber fisheries
a) Commercial, artisanal, subsistence: The harvest was with commercial ends between 1993 and 1994. At
present there are not fisheries of these species.
b) Estimated number of fishers: 10 fishermen, according to the decree that regulates the harvest of sea
cucumbers. Nevertheless, before the emission of the decree there was not a control of this situation.
c) Type of fishing methods and gear equipment used: Diving to lung, diving using compressor on board,
hose, regulator, boats, outboard motor.
d) Licensing/permitting requirements: According to the Decree N° 23138-MAG, publishing in La Gaceta
N° 80 on April 27, 1994: Licenses: 10
Requisites: 1-1200 sea cucumbers for fisherman per month
2- the fishing would be for two months per year
3- fishermen should land the product only in the ports of Cuajiniquil and Coco Beach.
4- fishermen will have to present a monthly report.
5- facilities for the process of the product must possess the permissions of
industrialization, marketing and conservation of fishing products.
215
e) Sea cucumber farming, if any: In Costa Rica does not exist sea cucumbers farming.
f) Preferred markets (live vs. dried): Does not arrange of information of markets, but they were
commercialized dried.
g) Identification of the most important uses of sea cucumbers: Information does not exist, but seemingly it
was for consumption.
h) Landing data (species, bycatch, kg, sizes, etc), if available: There is no landing data.
i)
Conservation measures (minimum harvesting size, closed areas, closed seasons, etc):
-
-
Minimum harvest size: 20 cm
Closed areas: only the crop was allowed between the bordering zone with Nicaragua and Punta
Mala in Costa Rica, except in Bay Cuajiniquil, Muñeco Island , Bay El Hachal and Bay Tomas and
in protected areas.
Closed seasons: only the crop was allowed between October and April.
3. Domestic and International Trade
a) Information on value, retail, wholesale prices and trends:
Value or price: 30-40 colons at the cost of 10 years ago (it is equivalent at present to 0.07 to 0.09 dollars)
exchange rates 1 $ = ¢ 425
Other information: There is no available data due to the fact that the activity of crop was left 10 years ago.
b) Export volumes, values and trends; import volumes, values and trends: There is no available data.
c) Information on key sea cucumber trading countries and territories: There is no information.
d) Trade controls and enforcement, including identification of specimens in trade: Before the decree there
was neither regulations nor control, as soon as the decree was published, the Headquarter of Fishing
Resources and Aquaculture realized control in the ports of discharge, in addition to the monthly reports
that there had to present the fishermen who had to include: number of captured individuals, zone of
harvest, invoices of selling of the product, date of selling, quantity and buyer.
e) Information on illegal, unreported and unregulated trade: There is no data.
f) Levels of domestic consumption, trends and trade: In Costa Rica there does not exist the habit of consuming
sea cucumbers.
216
HARVEST AND TRADE OF TREPANG
(FAR EAST SEA CUCUMBER) FROM THE RUSSIAN FAR EAST
TRAFFIC Europe-Russia
Far East sea cucumber (trepang) (Apostychopus japonicus, Selenka, 1867; old scientific name Stychopus
japonicus var. armatus, Selenka, 1867) lives along Primorie coast up to Vladimir Bay to the north, near
southern coast of Sakhalin island (Aniva Bay. isle of Moneron), along Korea peninsular and in the Yellow sea
up to 33° northern latitude. Some of the latest research shows that the different species inhabit waters near
Japan. Trepang lives on sea bottom at depth 20-50 m but could be found up to 150 m.
Trepang plays an important role in the littoral ecosystem as it adsorbs organics from bottom sediments (the
only big benthos species in the area). One animal could process bottom ground from the area of 10-50 m2
annually. Thus serious decrease in population of trepang could lead to intensification of eutrophication process
in littoral areas.
Trepang is traditionally in high demand in Eastern medicine and cuisine. It contains biologically active elements
such as tri-terpene glycosides. Sometimes trepang is called “sea ginseng” and believed to be effective for
prophylactics of many diseases including cancer and impotency.
Harvest of trepang started in the region since the end of 19 century. At present the main technique is a diving.
In 1970es the day norm for one boat (3 divers) was 242 kg (raw weight). According to the Pacific Institute of
Fishery and Oceanography the trepang stock in Peter the Great Bay in 1970 was 6,030 tons (21,600 tons in
1959); about 1800 tons in Aniva Bay. Only 5% were matured animals good for harvest. Due to extensive
harvest and several unfavorable for breading years total catch decreased significantly by the year 1977 (1970
– 274 tons; 1975 – 150 tons; 1977 – 35 tons). As a result the trepang harvest in Primorie was prohibited since
1978, and since 1980 on Sakhalin. At that time according to the experts the official harvest by state organizations
was almost equal to private. By the year 1998 the stock of trepang in Primorie waters was estimated at about
300 tons (but the last real field census had taken place in 1970). Additional factors threatening trepang population
are harvest during spawning period and harvest of animals at early estrus period.
Intensive illegal harvest started since the catch ban was established. Initially it was harvested for restaurant
business but since early 1990s the main destination became China. Very soon harvest of trepang from small
private business was converted into well organized and centralized criminal activity. Cost of raw trepang at
black market is $2.5-4 per kilogram or $85-120 for kg of dried trepang (boiling and drying reduce weight by
16 times). Average cost of 1 dry kg at the Chinese border is USD100.
In some locations up to 80% of local male population is involved into this business, which is localized by
several areas of trepang habitats. Usually dry trepang is going for export. Only in Peter the Great Bay about
300 ????????? are involved who harvest about 160 tons (in dry weight worth at 1 million USD). Far East
Customs Department reported about 10 tons of seized dry trepang during 1995-1999 and 554 kg in 2001.
Usually trepang is traded in large stocks.
The real status of the population and harvest pressure are unknown. The evidences and interview with locals
and specialists show that trepang is already extinct in some areas and its population is decreasing rapidly.
217
NATIONAL REPORT – PAPUA NEW GUINEA
Jeff Kinch
Motupore Island Research Centre, University of Papua New Guinea
INTRODUCTION
The tropical fisheries for beche-de-mer in Papua New Guinea (PNG) is one of the most important sources of
income for rural coastal and island villagers throughout the country. The beche-de-mer fishery in PNG has a
direct impact to the sociological and economic well being of communities as it allows for greater participation
than any other fisheries in PNG. It assists in maintaining rural social stability by providing income-earning
opportunities in remote locations where other earning opportunities are limited. Due to the simple, low technology
methods of processing, it is an ideal commodity for rural areas as it does not require large capital outlays and
can be stored for long periods without deterioration and without the need for immediate transport.
The income derived by coastal communities from the sale of beche-de-mer has increased dramatically throughout
the 1990's in PNG. The large increase in production of beche-de-mer can be attributed to the decline in copra
prices, the effects of drought in previous years, increased fishing for beche-de-mer in remote locations, a
decline in the value of trochus and blacklip, and the establishment of new markets for previously low-value or
non-commercial species, associated with the economic boom experienced by China. The diversity of bechede-mer is now being altered in some areas due to this intensified and extensive exploitation and thus represents
a threat to community livelihood strategies, and the fishery itself.
There is a need for a positive long-term impact on the development of the beche-de-mer fishery in a sustainable
manner whilst maximising long term yields from the fishery.
1. Information on wild populations
In PNG, populations of commercial beche-de-mer are thought to be found in the Milne Bay, Manus, New
Britain, New Ireland, Western and Central Provinces (DPI, 1983). Previous surveys have been limited to
several species found in coastal lagoons along the South Papuan Coast (Shelly, 1981), and in some areas of
New Ireland (Tenakanai, 1991), Madang (Lokani et al, 1992), Western (Mohiba et al,1993), Milne Bay
(Lindholm, 1978; DFMR, no date; Chesher, 1980; Lokani et al, 1997; Skewes et al, 2002), Manus (Lokani
and Chapau, 1992) and New Britian (Mobiha et al, 2000; Gisawa, 2002). See Annex 1 for distribution
table.
The PNG National Fisheries Authority has an active stock assessment program, and surveys are ongoing
around the country. Further follow up work is still required if the beche-de-mer fishery in PNG is to remain
viable. There has been no annual surveys done during closure and prior to opening to assess the inter-annual
change in stock variability.
218
2. Nature of sea cucumber fisheries
a) Culinary and Traditional Usage
With some exceptions, beche-de-mer does not appear on either traditional or modern menus of most Melanesian
and Pacific communities, and thus the export trade does not conflict with local nutrition (except indirectly when
it draws fishermen and gardeners away from their normal activities). In PNG, black teatfish, H. fucogilva
(white teatfish), sandfish, and Thelenota ananus (prickly redfish) are consumed in different localities notably
Central, Manus, West New Britain, Milne Bay province and New Ireland Provinces (Shelley, 1986; Lindholm,
1978).
b) Harvesting
Traditional methods of harvesting of beche-de-mer in PNG are done either by hand-collection or free diving.
If it is in shallow enough water, people will wade across the reef collecting or if slightly deeper water, will dive
down and spear it with a lengthened spear. If it is in deeper water, a small harpoon embedded in a lead weight
will be dropped. The small harpoon punctures the beche-de-mer and brought by them to the surface. Dinghies are beginning to take the place of sailing canoes. The exporters sell them to villagers outright or on a hirepurchase scheme (see Smaalders and Kinch, 2003). The use of lights is a common practice. Hookah gear has
been used in recent years.
c) Processing
Beche-de-mer is produced by a process of boiling, cleaning, drying and smoking and requires the use of
boiling containers (typically discarded 200 litre oil drums); smoke sheds and racks, and large quantities of
firewood. The boiling and drying process is to preserve and prepare the product for marketing. Beche-demer is usually boiled for a period of 2-3 hours. The cooled, cooked beche-de-mer is then taken to the sea
where they are washed. Remnants of the stomach are then removed either by cutting down the length of the
body in the case of black teat, white teat and prickly redfish, or by reaming a stick down the inside of them in
the case of blackfish and greenfish. Prior to drying the body of beche-de-mer is opened wide and short sticks
are inserted across the body cavity. The function of the sticks is to hold the cut edges apart to allow the interior
to dry evenly by smoke and sun drying. Some are later wrapped in bark string or twine to ensure they achieve
the shape desired by the purchasers. Drying is a slow process taking several days. The drying racks are
usually housed in a small wooden stick-framed building covered with woven coconut palm fronds, which helps
to concentrate the heat and smoke. After the curing process is finished, the beche-de-mer is then packed in
copra or plastic sacks and delivered to market or sold to trade stores.
d) Sea cucumber farming, if any
There is no aquaculture of beche-de-mer in PNG though several proposals have been developed for it implementation.
e) Landing data
See Annex 2 for export figures.
219
f) Conservation measures
The need for the management of beche-de-mer fisheries in PNG was recognised from its inception in the 19th
century due to declining catches. In 1881 a closed season was attempted by the colonial government, but
failed to stop illegal fishing. In the early 20th Century attempts were made to manage the beche-de-mer at the
Trobriand Islands in the MBP with an Act in the Colonial Administration (Territoty of Papua, 1934).
Today, the National Fisheries Authority (NFA) has gazetted the National Beche-de-mer Management Plan
2001, for regulation and management of the industry and the implementation of Provincial Management
and Advisory Committees. The objectives of the National Management Plan are to manage the beche-demer fishery so that Papua New Guinea gains the maximum economic benefits from the fishery; to ensure that
the development of the bêche-de-mer fishery benefits coastal communities, particularly customary users; and
to ensure use of the bêche-de-mer resource is sustainable and that bêche-de-mer fishing has minimal impact on
the marine and coastal environment.
One issue that needs to be recognised is the lack of extension for fishers on minimum size limits, appropriate
collection and processing techniques. This has resulted in a loss of potential income and depletion of future
stocks through the indiscriminate collection and subsequent rejection of undersized bêche-de-mer. Also a
proportion of animals are rejected by purchasers due to decomposition caused by incomplete processing,
drying and improper storage. Diving at night with torches and with under water breathing devices is prohibited.
Table 1. Size Limits for Beche-de-mer from the National Management Plan
High Value Species Scientific Name
Live Length Dry Length
(cms)
(cms)
Sandfish
Holothuria scabra
22
10
Black Teatfish
H. nobilis
22
10
White Teatfish
H. fuscogilva
35
15
Greenfish
Stichopus chloronotus
20
10
Curryfish
S. variegatus
25
10
Prickly Redfish
Thelenota ananus
25
15
Surf Redfish
Actinopyga mauritiana
20
8
Blackfish
A. miliaris
15
10
Stonefish
A. lecanora
15
10
Low Value Species
Scientific Name
Tigerfish
Brown Sandfish
Chalkfish
Flowerfish
Amberfish
Lollyfish
Elephant Trunkfish
Pinkfish
Snakefish
Deepwater Redfish
Bohadschia argus
B. vitiensis/B.marmorata
B. similes
B. graeffei
Thelenota anax
Holuthuria atra
H. fuscopuntata
H. edulis
H. leucospilata
Actinopyga echinites
220
Live
(cms)
20
20
25
20
30
45
25
25
Length Dry Length
(cms)
10
10
7
10
15
15
10
15
Currently the compulsory closed season will occur each year from October 1-January 15 or when the TAC is
reached. Each province has a set TAC.
An issue for the NFA who has responsibility for enforcing the TAC and the beche-de-mer fishery in the MBP
is that the TAC has been continuously exceeded in recent years. For example the TAC set for the MBP in
2000 was 60 metric tonnes, but records show that nearly 184 metric tonnes were exported. In 2001, the TAC
was set at 140 metric tonnes and nearly 210 metric tonnes was exported. The National Beche-de-mer
Management Plan 2001 has now been amended whereby if a province exceeds it’s TAC it has the amount
that is over deducted from the next year. There are currently moratoriums on harvesting in the Manus and
Western Provinces’ fisheries.
The PNG government is faced with the difficult decision of whether to take further management measures in
an effort to make the fishery sustainable (albeit at a lower level of catch, and without any assurance of success), or to accept the unsatisfactory ‘boom and bust’ cycle of harvesting and wait for a long-term recovery.
The latter is not in the interest of the fishery as slow recovery rates for depleted beche-de-mer populations
have been recorded for some beche-de-mer fisheries in the South Pacific.
Overall the enforcement of the management plan has been poor.
3. Domestic and international trade
a) History of Commercial Exploitation
The beche-de-mer fishery in PNG is documented from 1878 but was probably exploited earlier than that (see
Russell, 1970; Shelley, 1981). Beche-de-mer exports in PNG peaked in 1883 and then declined until 1888
where it peaked once again and declined again after. Factors contributing to this were the competition from
sandalwood and falling beche-de-mer prices (Lokani, 1995). During this period, the value of beche-de-mer
export for British New Guinea [Papua] ranged from 70-95% of all exports (see Lokani, 1990, 1995).
Anecdotal evidence suggests that exploitation of beche-de-mer in PNG declined in the latter half of the 19th
century probably because of over-fishing. The harvesting of beche-de-mer was also affected in the first half of
the 20th Century when the Chinese and Japanese markets were closed due to the Sino-Japanese War and
World War II. The volume of exports during the 1960s and 1970s was due to enterprising Chinese based in
Port Moresby, Samarai, Rabaul, Kavieng and Kieta (DFMR, no date). During the 1970s the only area of
PNG that was producing beche-de-mer in commercial quantities was the MBP.
All the commercially-exploited species of beche-de-mer are in the two families Holothuriidae and Stichopodidae
in the order Aspidochirotida. Currently 19 species of beche-de-mer are taken from PNG waters with most of
these being low value species and the fishery is currently changing from a low-volume, high-value fishery to a
high-volume, low-value trade.
b) Export volumes, values and trends
Like all of the other Melanesian countries experiencing the current boom, there are now many more different
beche-de-mer species being fished in than previously and prices have increased exponentially. Brown sandfish,
greenfish and Bohadschia similes (chalkfish) were not previously exported and some common names often
represent a number of species, particularly H. atra (lollyfish) and Actinopyga miliaris (blackfish). Some
species of previously low-value beche-de-mer have shown increases in prices between approximately
221
1,000-3,000 per cent indicating that the process of depletion could progress through the value chain if not
properly managed. This increase in value may also be due to market acceptance as previously unknown lowvalue product becomes better known to consumers
The MBP is the largest producing province in PNG and now contributes roughly 40% of the total exports. The
increased production, can also be related to declines in other provinces, notably Western and Manus and also
the opening up of previous unfished areas within the MBP.
c) Information on key sea cucumber trading countries and territories
All beche-de-mer exported from PNG is usually exported to Hong Kong (a Special Administrative Region of
the Republic of China), Singapore and Korea.
d) Licensing and permitting requirements
The beche-de-mer industry is a restricted activity under the laws of PNG and a non-citizen should not be
issued with any license, engage in any part of the domestic beche-de-mer fishing industry or finance any aspect
of the domestic industry. Despite this, non-citizens are still actively involved in the beche-de-mer fishery
throughout the country, usually they advance money to a local buyers in order that they can purchase product.
One major issue of smuggling activities is that there are no official records, which has serious implications for
the enforcement of the TAC.
CONCLUSION
Management of the beche-de-mer fishery in PNG is required to achieve sustainable levels because it provides
the only realistic self-generated source of cash to island and coastal communities. Since beche-de-mer stocks
are under increasing pressure from over-fishing some immediate steps need to be undertaken to limit the effort
exerted on the stocks as a loss of income and depletion of future stocks through the indiscriminate collection
and subsequent rejection of undersized bêche-de-mer will cause dire social problems.
Management strategies that could be tested include having TACs at the Local level Government level and for
certain species with low abundances it maybe necessary to implement specific closures on these species by the
setting of species specific TACs. Resources need to be allocated for awareness and capacity building at the
village level for management of these valuable resources. This would include extension and training materials
on processing and appropriate harvesting methods; village awareness of over fishing on resource sustainability;
the possible incorporation of traditional closed seasons or areas (the best means of policing closed areas may
be through village involvement) and limited entry.
Effective monitoring is necessary to prevent over-exploitation and depletion of beche-de-mer resources and
further study is required on models of resource extraction. There is a need to continue stock assessments;
monitor active fisheries and recovery rates; apply proper enforcement of recording of data; empowerment and
support for fisheries inspectors and monitoring of overseas market. Finally, the potential for hatchery and reseeding programs should be investigated.
222
Fig. 2 Boiling and processing beche-de-mer
223
References
Chesher, R. 1980. Stock Assessment: Commercial Invertebrates of Milne Bay Coral Reefs. Report
prepared for the Fisheries Division, Department of Primary Industries, Port Moresby, Papua New Guinea.
DFMR. 1979. Annual Fisheries Report. Port Moresby: Department of Fisheries and Marine Resources.
DFMR. No date. Fisheries Commodity Statement: Beche-de-mer. Fisheries Archive Paper No.: P179.
Port Moresby: Department of Fisheries and Marine Resources.
DPI. 1983. Beche-de-mer. Fishery Commodity Statement released by the Department of Primary Industry,
Port Moresby, Papua New Guinea.
Gisawa, L. 2002. A Survey of some of the Marine Resources of the South Coast Area of the East New
Britian of Papua new Guinea. Report to the National Fisheries Authority, Port Moresby, Papua New
Guinea.
Kailola, P. with Lokani, P. no date. Sea Cucumbers. Paper prepared for the National Fisheries Authority, Port
Moresby, Papua New Guinea.
Lindholm, R. 1978. Beche-de-mer Fishery. Internal Report prepared for the Department of Primary Industry,
Port Moresby, Papua New Guinea.
Lokani, P. 1990. Beche-de-mer Research and Development in Papua New Guinea. Beche-de-mer Information
Bulletin. 2: 8-10.
Lokani, P. 1991. Survey of Commercial Sea Cucumbers (Beche-de-mer) in the West New Britain Province,
Papua New Guinea. Report to the Department of Fisheries and Marine Resources, Kavieng, New Ireland
Province, Papua New Guinea.
Lokani, P. 1995. Beche-de-mer Fisheries in PNG. In DFMR. Fisheries Research Annual Report: 19911993. Research and Surveys Branch, Technical Report, No.: 95-04. Port Moresby: Department of Fisheries
and Marine Resources.
Lokani, P. and Chapau, M. 1992. A Survey of the Commercial Sedentary Marine Resources of Manus
Island. Report to the Department of Fisheries and Marine Resources, Kavieng, New Ireland Province,
Papua New Guinea.
Lokani, P. and Kubohojam, G. no date. Beche-de-mer Processing and Marketing in Papua New Guinea.
Report to the Department of Fisheries and Marine Resources, Kavieng, New Ireland Province, Papua
New Guinea.
Lokani, P.; Matato, S. and Ledua, E. 1997. Beche-de-mer Resource Assessment in Milne Bay Province.
Report to the National fisheries Authority, Port Moresby, Papua New Guinea.
Lokani, P.; Mobiha, A. and Wafy, A. 1992. (eds.). Marine Resources Survey of Madang Province. Report
to the Department of Fisheries and Marine Resources, Kavieng, New Ireland Province, Papua New Guinea.
Lokani, P.; Polon, P. and Lari, R. 1996. Management of Beche-de-mer Fisheries in the Western Province of
Papua New Guinea. Beche-de-mer Information Bulletin. 8: 7-14.
Mobiha, A.; Polon, P.; Lari, R. and Jogo, S. 1993. A Survey of the Marine Resources of the Daru Area in
Western Province of Papua New Guinea. Report to the Department of Fisheries and Marine Resources,
Kavieng, New Ireland Province, Papua New Guinea.
Mobiha, A.; Tumi, C. and Robinson, E. 2000. A Survey of some of the Marine Resources of the North
Coast Area of the East New Britian of Papua new Guinea. Report to the Department of Fisheries and
Marine Resources, Kavieng, New Ireland Province, Papua New Guinea.
Myint, T. 1996. Beche-de-mer Exports. Papua New Guinea National Fisheries Authority Newsletter. 2
(1): 20-21.
224
Russell, P. 1970. The Papuan Beche-de-mer Trade to 1900. Unpublished MA Thesis. Port Moresby: University
of Papua New Guinea.
Shelley, C. 1981. Aspects of the Distribution, Reproduction, Growth and ‘Fishery’ Potential of
Holothurians (Beche-de-mer) in the Papuan Coastal Lagoon. Unpublished M.Sc Thesis. University of
Papua New Guinea.
Shelley, C. 1986. The Potential for Re-introduction of a Beche-de-mer Fishery in Torres Strait. In Haines, A.;
Williams, D. and Coates, D. (eds.). Torres Strait Fisheries Seminar, Port Moresby, 11-14 February
1985. Canberra: Australian Government Publishing Service.
Skewes, T.; Kinch, J.; Polon, P.; Dennis, D.; Lokani, P.; Seeto, P.; Wassenberg, T. and Sarke, J. 2002.
Research for the Sustainable Use of Beche-de-mer in the Milne Bay Province, Papua New Guinea:
CSIRO Division of Marine Research Interim Report. A report prepared for the National Fisheries Authority,
Port Moresby, Papua New Guinea; and the Australian Centre for International Agricultural Research, Sydney,
New South Wales, Australia.
Smaalders, M. and Kinch, J. 2003. Canoes, Subsistence and Conservation in Papua New Guinea’s Louisiade
Archipelago. SPC Traditional Marine Resource Management and Knowledge Information Bulletin.
15: 11-21.
SPC. 1996. ICFMap Milne Bay Fieldwork. SPC Fisheries Newsletter. 79: 6-7.
Tenakanai, C. 1991. An Overview of the Exploitation and State of Stocks of Marine Sedenatary Resources
in Waters of New Ireland. Memorandum (file 3-3-7) to the Department of Fisheries and Marine Resources,
Kavieng, New Ireland Province, Papua New Guinea.
Territory of Papua. 1934. Proclamation: Pearl, Pearl Shell and Beche-de-mer Ordinance, 1911-1934, of
the Territory of Papua. Samarai: Territory of Papua.
225
Annex 1: Species Density for PNG
Maximum
Species
Mean
Density
Density
(No./ha)
(No./ha)
Holothuria
275
nobilis
9.75
(black teatfish)
16.83
0.18
H. fuscogilva
54
(white teatfish)
3.50
3.27
0.42
H. scabra
2,900.00
13,500
(sandfish)
19.13
22.23
Province
Reference
0.04
West New Britain
Manus
Madang
Milne Bay
West New Britain
Manus
Madang
Milne Bay
Central
Manus
Madang
Western
Milne Bay
Madang
Western
Milne Bay
Madang
Western
Milne Bay
Lokani, 1991
Lokani and Chapau, 1992
Lokani et al, 1992
Skewes et al, 2002
Lokani, 1991
Lokani and Chapau, 1992
Lokani et al, 1992
Skewes et al, 2002
Shelly, 1981
Lokani and Chapau, 1992
Lokani et al, 1992
Mobiha et al, 1993
Skewes et al, 2002
Lokani et al, 1992
Mobiha et al, 1993
Skewes et al, 2002
Lokani et al, 1992
Mobiha et al, 1993
Skewes et al, 2002
3.29
Madang
Lokani et al, 1992
Central
West New Britain
Manus
Madang
West New Britain
Madang
Milne Bay
West New Britain
Manus
Madang
Western
Milne Bay
Manus
Madang
Western
Milne Bay
West New Britain
Manus
Madang
Milne Bay
Manus
Madang
Milne Bay
West New Britain
Manus
Madang
Western
Milne Bay
West New Britain
Manus
Madang
Western
Milne Bay
Madang
Western
Milne Bay
Madang
Western
Milne Bay
Madang
Western
Shelly, 1981
Lokani, 1991
Lokani and Chapau, 1992
Lokani et al, 1992
Lokani, 1991
Lokani et al, 1992
Skewes et al, 2002
Lokani, 1991
Lokani and Chapau, 1992
Lokani et al, 1992
Mobiha et al, 1993
Skewes et al, 2002
Lokani and Chapau, 1992
Lokani et al, 1992
Mobiha et al, 1993
Skewes et al, 2002
Lokani, 1991
Lokani and Chapau, 1992
Lokani et al, 1992
Skewes et al, 2002
Lokani and Chapau, 1992
Lokani et al, 1992
Skewes et al, 2002
Lokani, 1991
Lokani and Chapau, 1992
Lokani et al, 1992
Mobiha et al, 1993
Skewes et al, 2002
Lokani, 1991
Lokani and Chapau, 1992
Lokani et al, 1992
Mobiha et al, 1993
Skewes et al, 2002
Lokani et al, 1992
Mobiha et al, 1993
Skewes et al, 2002
Lokani et al, 1992
Mobiha et al, 1993
Skewes et al, 2002
Lokani et al, 1992
Mobiha et al, 1993
Milne Bay
Skewes et al, 2002
Abundance
Range
(No./200 m²)
0.40-9.82
H. atra
(lollyfish)
H.
fuscopunctata
(elephant
trunkfish)
H. leucospilota
(snakefish)
Actinpyga
echinites
(deepwater
redfish)
A. lecanora
(stonefish)
A. mauritiana
(surf redfish)
0.00
80.04
0.00-17.00
9.81
18.21
0.00-0.02
1,800.00
12,500
4,025
105.50
6.69
25
0.86
0.02
304
9.50
38.69
0.00-0.21
A. miliaris
(blackfish)
0.12
36.9
4.34
0.00-0.75
0.12
Thelenota
ananus
(prickly redfish)
T. Anax
(amberfish)
Stichopus
chloronotus
(greenfish)
79
1.63
8.04
0.47
4.50
6.03
0.63
4,258
16.00
128.20
0.00-1.21
3.81
S. hermanii
(curryfish)
456
8.63
8.06
0.06-3.08
Bohadschia
graeffei
(flowerfish)
B. argus
(tigerfish)
B. vitiensis
(brown
sandfish)
B. marmorata
(brown
sandfish)
0.09
3.45
0.00-9.06
0.37
9.48
0.00-0.21
1.33
4.43
0.00-1.00
0.99
226
Annex 2: PNG Beche-de-mer Exports 1960 – 2001
Year
Quantity
Price in Kina Reference
1960
1,623
Lindohlm, 1978
1961
2,400
Lindohlm, 1978
1962
4,448
Lindohlm, 1978
1963
12,845
Lindohlm, 1978
1964
6,295
Lindohlm, 1978
1965
4,092
Lindohlm, 1978
1966
4,413
Lindohlm, 1978
1967
10,468
Lindohlm, 1978
1968
11,183
Lindohlm, 1978
1969
12,401
Lindohlm, 1978
1970-71 6,527
Lindohlm, 1978
1971-72 3,872
Lindohlm, 1978
1972-73 9,869
Lindohlm, 1978
1973-74 4,068
7,041
DFMR, no date
1974-75 1,214
2,590
Lindohlm, 1978; DFMR, no date
1975-76 1,665
4,470
Lindohlm, 1978; DFMR, no date
1977
5,325
13,297
Lindohlm, 1978
1978
5,903
Lindohlm, 1978
(Jan-Apr)
1979
1980
1981
1982
1983
1984
1,300
2,351
11,090
22,960
7,630
4,668
4,000
7,445
25,966
73,409
23,938.97
13,472.49
DFMR, 1979
Wright, 1986 cited in Kailola with Lokani,
Wright, 1986 cited in Kailola with Lokani,
Wright, 1986 cited in Kailola with Lokani,
Lokani and Kubohojam, no date; Lokani, 1990
Lokani and Kubohojam, no date; Kailola with
Lokani, no date; Lokani, 1990
1985
19,491
58,192.00
Lokani and Kubohojam, no date; Lokani, 1990
1986
119,376
361,336
Kailola with Lokani, no date
1987
192,055
591,009.22
Lokani and Kubohojam, no date; Lokani, 1990
1988
202,789
801,770.13
Lokani and Kubohojam, no date; Lokani, 1990
1989
194,896
1,146,584.85
Lokani, 1990
1990
238,923
Lokani and Kubohojam, no date;
626,047.50 4,637,807.43
Lokani and Kubohojam, no date; Gaudechoux,
1991
(Jan-Aug)
1993
1992
655,462.00 4,993,123.00
Myint, 1996
1993
499,489.46 3,044,843.86
Myint, 1996
1994
208,795.70 NFA database
1995
444,747.00 4,491,037.71
Myint, 1996
1996
586,201.80 7,872,385.78
NFA database
1997
505,402.40 7,683,437.15
NFA database
1998
678,848.85 16,892,866.13 NFA database
1999
394,682.45 11,023,884.90 NFA database
2000
607,311.06 16,311,191.35 NFA database
2001
482.281.40 17,196,625.33 NFA database
(Note: This Table is to be used as a guide only. All data supplied by the NFA database may
be incomplete as the database is still under development and all entries may have not yet be
included).
227
Recommendations of Advances in Sea Cucumber
Aquaculture and Management.
This document is an extract from Advances in Sea Cucumber Aquaculture and Management. 2004. Lovatelli,
A., C. Conand, S. Purcell, S. Uthicke, J.-F. Hamel & A. Mercier, eds. regarding the recommendations made
at the Workshop on Advances in Sea Cucumber Aquaculture and Management (ASCAM),
14-18 October 2003, Dalian, China.
Recommendations for sea cucumber fisheries and management – Sessions 1 and 2
From the reports presented during this workshop on sea cucumber fisheries and aquaculture, it was clear that
sea cucumbers in most countries are suffering from heavy exploitation and population depletion. The discussion
sessions were used to develop recommendations agreed by the participants.
During these discussions, it was recognized that a critical need is to establish and implement management plans
towards sustainability of adequate breeding populations of all fished species. Countries should also aim to
develop management plans prior to opening further fisheries - only one of the counties reported at this conference
(Cuba) had data of virgin stock biomass.
An overriding issue is the lack of information on appropriate management approaches and analytical tools. The
fact that over fishing and stock depletion is still occurring indicates that specific approaches are needed for
managing sea cucumber trading and fisheries.
Catches and processed products records
In order to manage the existing resources and regulate trade, data at the national level (on catches, processing
and exports) need to be collected. Because these activities demand human resources, governments should
incorporate these activities into the fishery section of their national budgets.
Statistics at national and international levels should be standardized to ease cross-referencing between countries.
Major points to be considered, as inaccuracies still appear in several countries:
•
Records on the main species or taxonomic groups should be made available to the public.
•
Wet weights should be recorded for landings, and it should be clearly defined if these are gutted or whole
animal wet weights (and, if possible, conversion factors between these given).
•
The grades and sizes need to be recorded in order to quantify the extent of harvests and processed
products.
•
The numbers of animals should also be listed in records, to allow an estimation of the sizes.
•
Data from processors should reflect the actual weight of the product forms (e.g. fresh, frozen, dried).
•
Compilation of the statistics should be the responsibility of the national authority.
•
If data are collected through exporters/ traders at the national level, regulations (and possibly penalties)
should be placed on the non-reporting of exports.
•
Double-reporting in trading (import and re-export) needs to be monitored and documented by regional/
international bodies.
•
A uniform taxonomic guide is needed for fishery workers and traders. This point will need some agreements
between scientists, as the names of several species changed recently.
228
Harvesting and post-harvesting methods and information
In many sea cucumber-producing countries, a large section of the harvest is produced as a sub-standard
product that enters international trade as low value items. In many cases, both fishermen and exporters fail to
realize the maximum value of the resource. Therefore technical assistance on post harvest handling, processing
and quality assurance is required in developing countries. This may reduce pressure on the existing sea cucumber
resources if fewer animals need to be harvested to earn equivalent money.
A strong recommendation was for the development of manuals and training courses/workshops for best practices
in post-harvest handling and processing. These should be presented in local languages and in simple terms.
These manuals should include, but not be restricted to, the following:
•
Fishing and handling methods to minimize damage of harvested animals
•
Post-harvest handling techniques
•
Updated and reliable methods for processing, established from both research and sourcing of existing
information. These should be described for different species, but recognizing differences in needs of different
buyers and markets
Additionally, research is needed to analyse the supply and demand for sea cucumbers with projections for the
next 15-20 years. In particular, it should be investigated as to what effect the large increase in production of A.
japonicus in China will have on the global market.
Socio-economics and legislation
Public awareness of sea cucumber fisheries should be raised at a range of levels to highlight their importance
and vulnerability to overfishing. Networking and cooperation among researchers and fishery workers should
be promoted. This could be achieved by forming associations for processors and traders, researchers, fishery
managers and farmers. Additionally, newsgroups via email or the internet would be valuable for exchange of
information.
Sea cucumber fishing is very important to the livelihoods of coastal communities, particularly artisanal and
small-scale fishers in developing countries. Therefore, socioeconomic issues in sea cucumber fisheries are
important and should be recognised and incorporated in fishery management programmes. In particular, livelihood
options should be made available to fishers if management regulation put restrictions on the fisheries, such as
bans on fishing.
International intervention (e.g. IUCN/CITES) may be needed to assist in the conservation and management of
sea cucumbers. However, caution should be exercised when intervening in or regulating trade for all regions, as
there are regional differences in the status of populations of sea cucumbers, habitats and environment. The
possibility to initiate listing in CITES Appendix 2 or 3 for certain countries should be examined and the effects
analysed. A sea cucumber species from South America and the Galapagos Islands were the first such animals
listed in Appendix 3.
229
Legislation should involve the following:
•
Participation of stakeholders (including fishers, processors, policy makers, managers, exporters) in
formulating management plans
•
Authority divested at local/customary level, in certain circumstances (e.g. Melanesian artisanal fisheries
with customary tenure)
•
Enforcement to ensure protection of sea cucumbers and their habitats
Stock assessment
Common methods of data collection and presentation of results should be developed for commercially exploited
species. However, it should be clearly recognized that ecological traits differ markedly amongst species, thus a
management as a multi species fishery is strongly discouraged.
Initial stock surveys should be conducted before a fishery commences in order to obtain information on the
virgin biomass. Monitoring the recovery of stocks after fisheries have been closed should also be encouraged.
Several key recommendations:
•
Habitat types (e.g. cover of sea grass or corals, sediment or substratum characteristics) should be recorded
for each survey unit (e.g. transect).
•
GPS waypoint referencing should be applied where possible. This technique will allow sites to be visualized
using GIS technology and can allow more accurate calculation of stock densities and, in certain circumstances,
distances between individual holothurians.
•
The size and spatial context of the populations need to be defined, in particular, the area surveyed and the
likely area occupied by the sub-population.
Management plans
Management plans for sea cucumbers fisheries should be conservative because stocks are vulnerable to
overfishing. The most incipient threat is the depletion of sustainable breeding populations that endangers natural
replenishment of populations.
The participants identified a number of recommendations for fisheries managers that should be followed to
prevent depletion of breeding stocks:
•
The collection of sea cucumbers using compressed air (either SCUBA gear or hookah) or weighted hooks
should be restricted. Bans on using compressed air can protect deep stocks, but caution should be given
because shallow stocks may be more important for spawning. In cases where SCUBA or “hookah” diving
is permitted, the divers need to be trained to avoid risk to life of the divers and adhere to accepted OH&S
guidelines, including the use of safe equipment.
•
A “code of conduct” should be promoted for responsible fishing practices. This would involve common
sense fishing practices such as not collecting under-sized sea cucumbers and preserving a proportion of the
populations to act as breeding stock.
•
Habitats should be protected as well as the resource. Authorities should endeavour to protect the ecosystems
in which sea cucumbers live and, conversely, recognize the important role that sea cucumbers play in
ecosystem processes. Where sea cucumber habitats have been damaged, rehabilitation should be considered.
230
•
Attention should be given to evaluating the occurrence and significance of sea cucumbers as by-catch in
trawl nets and dredges. These indiscriminate fishing methods can impact populations and habitat. By-catch
of sea cucumbers in other fisheries needs to be both researched and documented.
•
Sea cucumbers should be recognized as significant marine resources, whether fished or not. The management
of sea cucumbers should be embodied within the broader context of sustaining marine resources.
•
Regular monitoring of populations should be employed and, in the case of restocking or use of moratoria,
the recovery of depleted populations should be evaluated.
Fisheries regulations should aim to protect ample breeding populations of each species. If the populations of
any species are fished below levels perceived to be minimal for breeding populations, then bans or moratoria
should be placed to halt further fishing. For areas that have been closed to fishing by moratoria, the lifting of
fishing bans should only proceed after it is established that stocks are viable for reproduction and can sustain
fishing.
Critical Research Needs
Research and assistance should have a stronger emphasis in countries where sea cucumber fisheries are important,
where exploitation has been high, or where knowledge is critically lacking. Research should also be promoted
in a range of countries to test generalities among regions and cultures. The main research topics needing
attention are listed below.
1) Parameters for fishery models: Growth, mortality and recruitment
Most crucial is the need for research on growth rates, particularly in early stages (juveniles) in the wild. This
information must be gained from individual species obtained in laboratory and field studies. In addition, data
from several locations need to be available in order to know if patterns are general or location-specific.
Information on mortality and longevity in the wild are also needed, to allow sustainable catch rates to be
estimated.
Research on larval ecology and recruitment processes of holothurians is also needed to develop fishery models,
and these processes will be widely variable in space and time.
Maximum sustainable yields should be estimated for different types of sea cucumber fisheries, based on surveys
of stock size and estimates of recruitment, growth and natural mortality. In many cases, however, these data
may not be available. If this is the case, TACs should be set conservatively (e.g. assuming less that 10% of
virgin biomass can be taken) until subsequent monitoring of stocks, recruitment and catch data indicates that
catch rates could be increased without jeopardizing larval production and subsequent recruitment.
Moreover, TACs alone are not sufficient for the management because this tool does not consider the size
structure of existing stocks. A fishery could be made up of small animals, which are harvested at the expense of
egg production of the site.
2) Minimum stock size for viable breeding populations
Populations need to be maintained at a minimum threshold level to ensure successful reproduction in the wild.
This is because sea cucumbers use chemical cues to spawn and need to be close to mates in order for
fertilization of oocytes. Below such threshold densities of adults, populations will fail to repopulate naturally. A
disproportionate reduction of recruitment when densities of spawners are reduced has been termed the “Allee”
effect in the general ecological literature.
231
Studies are needed to establish the thresholds for minimum size of effective breeding populations to avoid Allee
effects. Some literature exists for other taxa, but research is needed on the research tools to establish this
threshold. Therefore, substantial information on fertilization kinetics, reproduction and chemical cues in
holothurians is required. Research related to population size-dependent reproductive success exists, but these
studies have long been considered theoretical aspects with little practical use and therefore not used by the
fisheries industries/program managers. This means, not only more research but also better distribution and
application of the existing literature is needed.
3) General ecological studies
In addition to studies on larval recruitment (see above), other studies should examine the factors affecting the
movement of sea cucumber larvae within the water column and factors influencing settlement. An understanding
of larval movement and settlement processes will improve predictions on dispersal and the likelihood of selfrecruitment and natural replenishment of populations. Specifically, more information is needed on the source
and sink of recruits for local populations.
General research tools are needed for collecting and analysing quantitative data on the ecology of sea cucumbers,
taking into consideration their seasonal and diurnal behaviours.
Information on the juvenile ecology of holothurians is sparse, but is needed.
Little research exists on the effects and benefits of sea cucumbers on ecosystem. Data available indicate that
removal of these animals could lead to major changes to the ecosystem, such as decreased overall productivity.
However, to confirm this effect, large-scale experimental work in multiple areas with natural densities and
over-fished areas must be conducted.
4) Effectiveness of MPAs or No-Take Zones and methods of management
Different modes of management have been used for sea cucumber fisheries but few cases, both of failures and
successes, have been documented. There is a need for a review that summarizes case studies where management
has worked and how participatory management can be used.
Knowledge on the effectiveness of MPAs (especially No-Take Zones) and comparison of a range of management
methods (such as broad fishery closure) should be collated. Research should also be encouraged to determine
the appropriate sizes, numbers and spatial design of MPAs, and to investigate if "spillover" effects from these
zones into fished areas occur. This could also include a review of existing literature and case studies on MPAs.
Research is needed generally for understanding which management tools/approaches are best for sea cucumber
fisheries and under which circumstances. This could include tax, regulating the number of fishers, fishing effort,
times, sites, sizes.
5) Stock delineation
Stock delineation and quantifying the extent of populations are important for managing stocks and understanding
recruitment. Such information is particularly relevant for restocking over broad spatial scales, due to likely
adverse effects on genetic diversity if genetically different stocks are mixed.
6) Taxonomy
The taxonomic status of some of the most valuable holothurian species is uncertain and recent studies indicated
the potential for the existence of a number of cryptic species among holothurians. Classical and genetic taxonomic
studies are needed to clarify the status of beche-de-mer species.
232
7) Restocking
Restocking is generally only a last resort if other management measures to recover a depleted fishery have
failed. Good management to preserve breeding populations should be the first solution, because there are risks
of changing genetic diversity of existing stocks when juveniles are released for restocking or stock enhancement.
Recommendations for restocking:
•
Definitive studies are needed about the economic viability and returns from restocking programs in which
hatchery-produced juveniles are released into the wild.
•
The value and significance of restocking to ecosystem functioning and long-term repopulation needs to be
included in cost-benefit analyses.
•
Release of hatchery-produced juveniles should only be conducted at sites with the same genetic stock as
the broodstock used for production. Translocation of animals into foreign grounds should be prohibited.
•
Spawners (both male and female) must be chosen in sufficient numbers to warrant genetic diversity and
gene frequencies in the offspring similar to that in the receiving areas.
•
The danger of the transfer of disease, parasites and introduced species from restocking programmes needs
to be controlled. Transfer protocols and disease checks need to be developed to ensure healthy juveniles
are used for restocking.
•
The carrying capacity of the habitat (in terms of both number and biomass) should be evaluated before
restocking.
•
Methods on the best strategies for releasing juveniles should be researched prior to restocking.
Recommendations for aquaculture – Session III
1. Dissemination of available data on sea cucumber aquaculture
The presentations and following discussions have brought to light a huge amount of knowledge. Several ways
to disseminate and share this information have been proposed.
Publication of a manual or guide on sea cucumber aquaculture. The chief recommendation made by the
participants of the workshop was to prepare and publish a reference manual that would compile the various
aquaculture techniques currently available or being developed for the main commercial species of sea cucumbers.
This practical guide should be well illustrated and be written in a clear accessible
language that would address the needs of prospective aquaculturists and farmers. It would indirectly provide
basic information on sea cucumber aquaculture to stakeholders and policy makers. Although it should first be
published in English, the book could eventually be translated to reach a broader audience, especially the
Chinese community who has made a significant contribution to this field. Topics that are likely to be covered in
such a manual include:
Hatchery techniques
o
Brood stock collection and handling
o
Spawning induction
o
Larval rearing
o
Early juvenile rearing
233
-
-
Farming/sea ranching techniques
o
Juvenile grow-out
o
Pond preparation/management
o
Co-culture with other species (polyculture)
General advice
o
Summary of cautions and known difficulties
o
Main components and basic costs of a sea cucumber aquaculture project
o
Glossary of technical and popular terms
Enhancement of international exchanges The bringing together of experts from the scientific, technical and
business aspects of sea cucumber aquaculture was another important outcome of the workshop. In order to
encourage collaboration and technology transfer, it has been suggested that a directory of specialists from the
different fields of activity be compiled and made available. It could include a complete listing of available
references pertaining to the main commercial species as well as a list of available directories/contacts pertaining
to import/exports and markets. This index of literature and experts should be accessible in print as well as
through the internet. An additional means of encouraging communication, cooperation and collaborative efforts
that has been proposed is the creation of workgroups and networks, perhaps through international agencies
such as the World Aquaculture Society.
Because communication relies on a certain degree of uniformity, consideration should be given to the
standardization of the vocabulary used to report the data in the future.
2. Suggestions for future research and development
The presentations and discussions have shown that although significant breakthroughs and advances have been
made by many teams in the field of sea cucumber aquaculture, a number of aspects still need to be investigated
in order to allow further development. This is especially true for tropical species of sea cucumbers being
cultivated in developing nations.
2.1 Fundamental biological research. Several problems in the culture of sea cucumbers stem from the lack
of basic knowledge on the general biology of both adults and juveniles. Main areas of research should include
reproduction, feeding ecology, substrate selection, predation on all life stages and chemical defences.
It has been suggested that hatchery-reared juveniles could develop a behavioural deficit that would lower their
survival rate once they are released in the field during the course of restocking procedures. This has to be
studied as well as the potential effect of captive-breeding on the presence or levels of bioactive substances in
the tissues, which have various roles: some can serve as defence mechanisms and other have properties that
are valued in processed products sold for human consumption.
A better knowledge of the diseases and parasites that affect all the life stages has to be acquired in order to
identify the causal agents of the major culture failures, and discriminate between the deleterious and potentially
beneficial species that live in association with sea cucumbers.
234
2.2 Hatchery techniques. Most of the existing methods used to induce spawning in sea cucumbers are still not
very reliable. Furthermore, the common practice of shocking the brood stock (thermally or mechanically) is
suspected to result in the shedding of immature or deteriorated gametes. Alternative methods for spawning
induction should be investigated to maximize both the quantity and quality of gametes obtained, and optimise
the success of the cultures.
Metamorphosis from pelagic to benthic forms remains a crucial step in sea cucumber aquaculture during which
high mortality rates are recorded. Hence, investigation of settlement requirements and preferences should
remain a priority. The formulation of feeds should also be studied to improve the growth and survival rates of
the larval and juvenile stages.
Another important research area is the control of disease outbreak in aquaculture. The uncontrolled utilization
of antibiotics is a growing concern. Their effect on the sea cucumbers themselves, on the environment and on
the eventual consumers should be investigated closely and alternatives developed and promoted.
2.3 Farming/sea ranching. For the species that have been successfully reared to juveniles, methods used in
the growout of post-metamorphic stages should be improved to maximize cost-effectiveness. More specifically,
different factors pertaining to the preparation and optimisation of ponds and sea ranching sites (habitats,
substrates, enclosure materials, control of environmental factors, etc.) could be studied.
The possibility of recycling abandoned infrastructures used to grow other marine species to meet the needs of
sea cucumber aquaculture should be assessed, as well as the prospects for co-culture of sea cucumbers with
other commercial species, either simultaneously or successively.
3. General preoccupations
Even though the purpose of the workshop was to gather knowledge from different experts in order to promote
and help in the development of sea cucumber aquaculture, several participants have expressed a number of
concerns. One of the concerns is the potential effect that commercial-size aquaculture facilities could have on
the environment. As the industry develops, the benefit and usefulness of farming and sea ranching in different
environments and countries should be addressed and weighed against the cultural and environmental costs.
Ultimately, guidelines for ethics and conservation measures should be developed and promoted.
235
LIST OF PARTICIPANTS
Australia
Mr Stephen SLY
Aquatic Resource Manager - ESD
Department of Business, Industry & Resource Development – Fisheries Group
GPO Box 3000
Darwin NT 0801
AUSTRALIA
Tel.: +61 (8) 89 99 23 93
Fax: +61 (8) 89 99 20 65
Email: steve.sly@nt.gov.au
China
Mr LU Xiaoping
Chief
Division of Fauna Affairs
CITES Management Authority of China
18 Hepingli East St.
Beijing 100714
P.R. CHINA
Tel.: +86 (10) 84 23 90 01
Fax: +86 (10) 64 21 41 80
Email: lxpc@263.net
Mr He Jianxiang
Deputy Chief
Division of Aquatic Wildlife Administration
Aquatic Wild Fauna and Flora Administrative Office
Ministry of Agriculture
No.11 Nongzhanguan Nanli
Beijing 100026
P.R. China
Tel: +86-10-6419 3273
Fax: +86-10-6419 3100
Email: fisheryccf@agri.gov.cn
Mr KWAN Sai-Ping (Boris)
Endangered Species Protection Officer
Agriculture, Fisheries & Conservation Dept
6/F Cheung Sha Wan Government Offices
303 Cheung Sha Wan Road
Kowloon, Hong Kong (SAR)
CHINA
Tel.: +85 (2) 21 50 69 82
Fax: +85 (2) 23 77 44 13
Email: boris_sp_kwan@afcd.gov.hk
Mr CHOW Wing Kuen
Acting Senior Fisheries Officer
Aquaculture Fisheries
8/F Cheung Sha Wan Government Offices,
303 Cheung Sha Wan Road, Kowloon,
Hong Kong (SAR), CHINA
Tel: (852) 2150 7090
Fax: (852) 2314 2866
Email: wk_chow@afcd.gov.hk
Cuba
Ms Irma ALFONSO HERNÁNDEZ
Sea Cucumber Project Leader
Fisheries Research Center
5ta Ave. #246, Sta Fé, Barlovento.
Mpio. Playa. Ciudad de La Habana
CUBA CP 19 000
Tel.: +57 (7) 209 80 55
Fax: +57 (7) 204 58 95
Email: irma@cip.telemar.cu
236
Ecuador
Mr Manfred ALTAMIRANO
Charles Darwin Foundation
P. O. Box 17-01-3891
Quito ECUADOR
Fax: +593 (52) 527 425 (ext 3)
Email: maltamirano@fcdarwin.org.ec
Ms M. Verónica TORAL-GRANDA
Sea Cucumber Research Group - Coordinator
Charles Darwin Foundation
P. O. Box 17-01-3891
Quito ECUADOR
Tel.: +593 (52) 527 425 (ext 221)
Fax: +593 (52) 527 425 (ext 3)
Email: vtoral@fcdarwin.org.ec
vtoral@excite.com
Fiji
Mr Stanley A. QALOVAKI
Researcher (Resource Assessment)
Department of Fisheries
Research Division
Queen’s Highway
Draunibota, Lami FIJI
Tel.: +679 336 11 22
Fax: +679 336 11 84
Email: sqalovaki@fisheries.gov.fj
Indonesia
Mr Asep SUGIHARTA
Head Section of Foreign Traffic Control on Flora & Fauna Utilisation
Directorate of Biodiversity Conservation
Ministry of Forestry
Manggala Wanabakil Building, Block VII, Floor 7
Jalan Gatot Subroto
Jarkata INDONESIA
Tel.: +62 (21) 572 02 27
Fax: +62 (21) 572 02 27
Email: cites@dephut.cbn.net.id
Jamaica
Dr Karl A. AIKEN
Lecturer in Life Sciences
Department of Life Sciences
University of the West Indies
Mona Campus
Kingston 7 JAMAICA, West Indies
Tel.: +(876) 927 12 02
Fax: +(876) 977 10 75
Email: karl.aiken@uwimona.edu.jm
237
Japan
Mr Shingo FUKUI
Ecosystem Conservation Officer
Fisheries Agency
Government of Japan
1-2-1 Kasumigaseki, Chiyoda-ku
Tokyo 100-8907 JAPAN
Tel.: +81 (3) 35 02 07 36
Fax: +81 (3) 35 02 16 82
Email: shingo_fukui@nm.maff.go.jp
Malaysia
Assoc. Prof. Ridzan HASHIM
University Islam Antarabangsa (UIA)
MALAYSIA
Mr Zaidnuddin ILIAS
Fisheries Research Officer
Department of Fisheries Malaysia
Turtle & Marine Ecosystem Center
23050 Rantau Abang
Dungun, Teregganu MALAYSIA
Tel.: +60 (9) 845 81 69
Fax: +60 (9) 845 80 17
Email: zaiali01@yahoo.com
Mr Jackson CLIVE JUSAN
Department of Fisheries Malaysia
Level 8 & 9, Wisma Tani
Jalan Sultan Salahuddin
50628 Kuala Lumpur
MALAYSIA
Tel.: +60 (3) 26 17 56 12
Fax: +60 (3) 26 94 29 84
Email: jack_clive@yahoo.com
Ms Thalathiah SAIDIN
Director Fish Health & Quality Assurance Division
Department of Fisheries Malaysia
Level 8 & 9, Wisma Tani
Jalan Sultan Salahuddin
50628 Kuala Lumpur MALAYSIA
Tel.: +60 (3) 26 17 56 16
Fax: +60 (3) 26 98 02 27
Email: thalathiah@hotmail.com
Mr LOO Kean-Seong
CITES Officer
Department of Wildlife & National Parks
KM 10, Jalan Cheras
56100 Kuala Lumpur
MALAYSIA
Tel.: +60 (3) 90 75 28 72 (ext 163)
Fax: +60 (3) 90 75 28 73
Email: looks@wildlife.gov.my
Mr Ahmad ALI
Research Officer
Marine Fishery Resources Development &
Management Development (MFRDMD)
21080 Chendering, Terengganu
MALAYSIA
Tel.: +60 (9) 616 31 50
Fax: +60 (9) 617 51 36
Email: aaseafdec@mfrdmd.org.my
Ms Suhaila MOHD. OMAR
Assistant Lecturer
International Islamic University Malaysia
Kulliyyah of Science, IIUM
Jalan Gombak
53100 Gombak, Kuala Lumpur
MALAYSIA
Tel.: +60 (3) 20 56 40 00 (ext 3379)
Email: combizo@hotmail.com
238
Malaysia (continued)
Mr Ahmad Saktian LANGGANG
Section Head of Resource Management
Department of Fisheries Malaysia
Level 8 & 9, Wisma Tani
Jalan Sultan Salahuddin
50628 Kuala Lumpur
MALAYSIA
Tel.: +60 (3) 26 17 56 47
Fax: +60 (3) 26 91 03 05
Email: saktian@dof.moa.my
Mr Yusof SHARIFF
Wildlife Officer
Department of Wildlife & National Parks
KM 10, Jalan Cheras
56100 Kuala Lumpur
MALAYSIA
Tel.: +60 (3) 90 75 28 72 (ext 233)
Fax: +60 (3) 90 75 28 73
Email: yusoff@wildlife.gov.my
Ms Rozeta ZAHARAN
Wildlife Officer
Department of Wildlife & National Parks
KM 10, Jalan Cheras
56100 Kuala Lumpur
MALAYSIA
Tel.: +60 (3) 90 75 28 72
Fax: +60 (3) 90 75 28 73
Email: rozeta@wildlife.gov.au
Mr Ramli KHAMIS
Fisheries Officer
Department of Fisheries Malaysia
Level 8 & 9, Wisma Tani
Jalan Sultan Salahuddin
50628 Kuala Lumpur
MALAYSIA
Tel.: +60 (3) 26 17 54 93
Fax: +60 (3) 26 91 03 05
Mr Sukarno WAGIMAN, Head
Section of Resources Rehabilitation & Recreational Fishery
Department of Fisheries Malaysia
Level 8 & 9, Wisma Tani
Jalan Sultan Salahuddin
50628 Kuala Lumpur
MALAYSIA
Tel.: +60 (3) 26 98 25 00
Email: sukarnow@hotmail.com
Mr Sim YEE KWANG
Research Officer
Muka Head Marine Research Station
Universiti Sains Malaysia
11800 Minden, Penang
MALAYSIA
Tel.: +60 (4) 653 38 88 (ext 2195)
Fax: +60 (4) 656 36 72
Email: mrsimyk@yahoo.com
Mrs Zaihatun Mahani ZAKARIAH
Researcher (Maritime Policy)
Maritime Institute of Malaysia (MIMA)
B-06-08-B-06-11, Megan Avenue II
Jalan Yap Kwan Seng
50450 Kuala Lumpur
MALAYSIA
Tel.: +60 (3) 21 61 29 60
Fax: +60 (3) 21 61 70 45
Email: zahaitun@mima.gov.my
Mr Sufian AHMAD
Fisheries Officer
Department of Fisheries Malaysia
Agricultural Ministry Malaysia
Level 8 & 9, Wisma Tani
Jalan Sultan Salahuddin
50628 Kuala Lumpur
MALAYSIA
Email: sufian7174@yahoo.com
sufian@dof.moa.my
Mr Alvin WONG
Ketua Cawangan Pengurusan Sumber
PPN Sabah
MALAYSIA
239
Malaysia (continued)
Mr Azhar NORAINI
Principal Assistant Director
Ministry of Science, Technology & the Environment (MOSTE)
Block L5, Parcel C
Federal Government Administrative Centre
Putrajaya
MALAYSIA
Tel.: +60 (3) 88 85 80 27
Fax: +60 (3) 88 89 29 73
Email: nazhar.01@yahoo.com
azhar@@moste.gov.my
Mexico
Ms Maria Dinorah HERRERO PEREZRUL
Profesor Investigador “C”
CICIMAR-IPN
Ave. IPN S/N. Col. Playa Palo de Santa Rita
C.P. 23096
La Paz, B.C.S.
MEXICO Apdo 592
Tel.: +52 (612) 122 53 66
Fax: +52 (612) 122 53 22
Email: dherrero@ipn.mx
dainoper@hotmail.com
Philippines
Ms Ludivinia L. LABE
Officer-In-Charge, Marine Invertebrate Research Section
BFAR / National Fisheries Research & Development Institute
940 Kayumanggi Press Bldg
Quezon Ave
Quezon City 1100
PHILIPPINES
Tel.: +63 (2) 372 50 62
Fax: +63 (2) 372 50 63
Email: lubbai@yahoo.com
luvil@nfrdi.da.gov.ph
240
United States of America
Mr John FIELD
Fisheries Biologist
U.S. Fish & Wildlife Service
4401 N. Fairfax Drive, Room 750
Arlington, VA 22203
U.S.A.
Tel.: +1 (703) 358 24 96
Fax: +1 (703) 358 22 76
Email: john_field@fws.gov
Organizations
Mr Alessandro LOVATELLI
Fishery Resources Officer (Aquaculture)
Inland Water Resources & Aquaculture Service
FAO - Fishery Resources Division
Viale delle Terme di Caracalla
00100 Rome
ITALY
Tel.: +39 (06) 57 05 64 48
Fax: +39 (06) 57 05 30 20
Email: alessandro.lovatelli@fao.org
Dr Kim J. FRIEDMAN
Kim Friedman
Senior Reef Fisheries Scientist
Secretariat of the Pacific Community (SPC)
B.P. D5-98848 Noumea Cedex
NEW CALEDONIA
Tel: +(687) 26 54 74
Fax: +(687) 26 38 18
Email: kimf@spc.int
Mr Glenn SANT
Director, TRAFFIC Oceania
GPO Box 528
Sydney NSW 2001
AUSTRALIA
Tel.: +61 (2) 92 80 16 71
Fax: +61 (2) 92 12 17 94
Email: gsant@traffico.org
241
Experts/Resource participants
Prof Chantal CONAND
Emeritus Professor
Laboratoire ECOMAR
Université de La Réunion
97715 Saint-Denis mes. Cx 9
FRANCE
Tel.: +(262) 262 93 81 30
Fax: +(262) 262 93 86 85
Email: conand@univ-reunion.fr
Mr James COMPTON
Regional Director, TRAFFIC Southeast Asia
Unit 9-3A, 3rd Floor
Jalan SS23/11, Taman SEA
47400 Petaling Jaya
Selangor
MALYSIA
Tel.: +60 (3) 78 80 39 40
Fax: +60 (3) 78 82 01 71
Email: james.compton@po.jaring.my
Dr Andrew BRUCKNER
Coral Reef Ecologist
NOAA Fisheries
Coral Reef Conservation Program
Office of Habitat Conservation
1315 East West Highway
Silver Spring, MD 20910
U.S.A
Tel.: +(301) 713 34 59 (x 190)
Fax: +(301) 713 01 74
Email: andy.bruckner@noaa.gov
Mrs Noorainie AWANG ANAK
Country Coordinator, TRAFFIC Southeast Asia
Unit 9-3A, 3rd Floor
Jalan SS23/11, Taman SEA
47400 Petaling Jaya
Selangor
MALAYSIA
Tel.: +60 (3) 78 80 39 40
Fax: +60 (3) 78 82 01 71
Email: naatsea@po.jaring.my
Mr Warwick NASH
OIC, World Fish Center – Pacific Office
World Fish Center
c/- Secretariat of the Pacific Community (SPC)
B.P. D5-98848 Noumea Cedex
NEW CALEDONIA
Tel.: +68 (7) 26 01 31
Fax: +68 (7) 26 38 18
Email: w.nash@cgiar.org
Ms Elizabeth A. BURGESS
Consultant, TRAFFIC Southeast Asia
Unit 9-3A, 3rd Floor
Jalan SS23/11, Taman SEA
47400 Petaling Jaya
Selangor
MALAYSIA
Tel.: +60 (3) 78 80 39 40
Fax: +60 (3) 78 82 01 71
Email: lizardtravels@yahoo.com.au
Mr David L. PAWSON
Senior Scientist
National Museum of Natural History
Mail Stop MRC163
Smithsonian Institution
Washington DC 20013-7012
U.S.A.
Tel.: +(202) 786 21 27
Fax: +(202) 357 30 43
Email: pawson.david@nmnh.si.edu
Dr Mark BAINE
Director, Motupore Isl& Research Centre
University of Papua New Guinea
P. O. Box 320
University 134, National Capital District
Papua New Guinea
Tel.: +(675) 325 46 45
Fax: +(675) 325 46 45
Email: bainemsp@upng.ac.pg
242
Dr Andrew J. LAWRENCE
Senior Lecturer
Aquatic Ecology & Resource Management
Department of Biological Sciences
University of Hull
Cottingham Road
Hull HU6 7RX
UNITED KINGDOM
Tel:
+44 (0) 1482 46 53 98
Fax: +44 (0) 1482 46 54 98
Email: a.j.lawrence@hull.ac.uk
r Yves SAMYN
CBD-National Focal Point
Assistant, Tutor for the Global Taxonomy Initiative
Royal Belgium Institute of Natural Sciences
Vautierstraat 29
B-1000 Brussels
BELGIUM
Tel.: +32 (2) 627 43 41
Fax: +32 (2) 627 41 41
Email: yves.samyn@naturalsciences.be
cbd-gti@naturalsciences.be
Mr Jeffery P. KINCH
Regional Community Development Officer-Pacific
Marine Aquarium Council
P. O. Box S23, MH Superfresh
Tamavua, Suva
FIJI
Tel.: +67 (9) 337 13 00
Fax: +67 (9) 337 17 73
Email: jeffkinch@connect.com.fj
Mr Philip LAMBERT
Curator of Invertebrates
Royal British Columbia Museum
675 Belleville St.
Victoria, British Columbia
V8W 9W2
CANADA
Tel.: +(250) 387 65 13
Fax: +(250) 356 81 97
Email: plambert@royalbcmuseum.bc.ca
Mr Grant LEEWORTHY
Fisheries Research Manager
Tasmanina Seafoods P/L
13-17 Redgum Drive
Dandegong South, VIC 3175
AUSTRALIA
Tel.: +61 (3) 97 68 36 15
Fax: +61 (3) 97 68 36 16
Email: grantl@tasmanianseafoods.com.au
Dr Jun AKAMINE
Professor
Nagoya City University
Nagoya
JAPAN
Tel.: +81 (52) 872 58 12
Fax: +81 (52) 872 58 12
Email: akamine@hum.nagoya-cu.ac.jp
Mr Allen HANSEN
Managing Director
Tasmanina Seafoods P/L
PO Box 239
Smithton, TAS 7330
AUSTRALIA
Tel.: +61 (3) 64 52 12 75
Fax: +61 (3) 64 52 20 47
Email: allenh@tasmanianseafoods.com.au
Mr Gilbert HANSON
Manager
Tasmanina Seafoods P/L
13-17 Redgum Drive
Dandenong South, VIC 3175
AUSTRALIA
Tel.: +61 (3) 97 68 36 15
Fax: +61 (3) 97 68 36 16
Email: gilberth@tasmanianseafoods.com.au
243
Animals Committee Members
Dr Mohammad POURKAZEMI
International Sturgeon Research Institute
P.O. Box 41635-3464
RASHT
Iran (Islamic Republic of)
Tel.: +98 (131) 660 65 03
Fax: +98 (131) 660 65 02
Email: pkazemi_m@yahoo.com
Dr Choo-hoo GIAM
CITES Animals Committee Member
78 Jalan Haji Alias
SINGAPORE 268559
Tel.: +65 64 66 64 86
Email: giamc@singnet.com.sg
CITES Secretariat
Mr Tom DE MEULENAER
Acting Chief
Scientific Support Unit
CITES Secretariat
International Environment House
Chemin des Anémones
1219 CHATELAINE, Genève
SWITZERLAND
Tel.: +41 (22) 917 81 31
Fax: +41 (22) 797 34 17
Email: tom.de-meulenaer@unep.ch
Ms Paula HENRY
Scientific Support Unit
CITES Secretariat
CH-1219 Ch telaine,
International Environmental House
Chemin des Anémones
1219 CHATELAINE, Genève
SWITZERLAND
Tel.: +41 (22) 917 81 31
Fax: +41 (22) 797 34 17
Email: paula.henry@unep.ch
244