Appearance
Adults are usually 20–35 mm long. The skin and flesh are watery and fairly transparent. The colour of the skin varies between light greyish-brown to almost black. Close inspection reveals fine dark spotting usually over the whole body; this shows up better in alcohol-preserved specimens. Often, but not always, the respiratory pore is pale and unspotted. The mucus is colourless.Particularly in North America, some "Deroceras laeve" grow large enough that they closely resemble "D. invadens". A useful clue to distinguish them is the profile of the end of the tail when the animal has been disturbed or is preserved. The tail of "D. invadens" usually slants vertically upward from the sole for a short distance, or even bends backwards. The tail of "D. laeve" slopes forward above the sole. Also, the tail of "D. invadens" is longer than the mantle, whereas it is the same length or shorter in "D. laeve".
Nevertheless, dissection is required to distinguish "D. invadens" reliably from "D. laeve" and from various similar "Deroceras" species occurring in Europe, such as "Deroceras sturanyi", the true "Deroceras panormitanum", and "Deroceras golcheri". Reise et al. discuss and figure the most critical anatomical characters. In most populations of "D. invadens", the proximal penis has two side pockets; these have roughly equal widths and both have rounded, stout ends. A prominent appending penial gland with 3–7 branches attaches between the caecum and lobe on the dorsal side; these branches are less knobbly in outline than those of "D. panormitanum". The penial retractor muscle attaches between the caecum and lobe on the ventral side. The intestinal caecum is either absent or represented merely by a widening of the rectum. Barker and Sirgel detail various other aspects of the anatomy.
Distribution
The distribution has been extensively reviewed by Hutchinson et al.. The native range is thought to be Italy but the first certain record is from Britain in 1930. "Deroceras invadens" now occurs in very many other parts of the world, although there is only one record from Asia. The list below gives dates of first reports; oceanic Islands are considered separately at the end.Europe
⤷ Italy – believed native
⤷ Great Britain – 1930
⤷ Denmark – 1937
⤷ France – 1945
⤷ Sweden – c. 1957, ≤1980
⤷ Ireland – 1959
⤷ Finland – ≤1961, ≤2014
⤷ Norway – 1967, 1983
⤷ Belgium – 1968
⤷ Netherlands – 1969
⤷ Spain – 1974
⤷ Portugal – 1977
⤷ Austria – 1977
⤷ Germany – 1978
⤷ Switzerland – 1982
⤷ Czech Republic – 1996
⤷ Luxembourg – 1997
⤷ Poland – 2001
⤷ Slovakia – 2003
⤷ Greece – 2011
⤷ Monaco – 2012
⤷ San Marino – 2013
⤷ Montenegro - 2014
Earlier records of ""D. panormitanum" sensu lato" from south-eastern Europe should be rechecked, given the taxonomic confusion prior to 2011; records from Romania, Lithuania and Hungary are erroneous or unconfirmed.
Africa
⤷ South Africa – 1963
⤷ Egypt – 2005–7
⤷ Kenya – 2012
Asia and Australasia
⤷ Israel – 2013
⤷ Australia – 1936
⤷ New Zealand – 1974
North America:
⤷ USA: California, Washington State and Oregon, Colorado, Utah, Washington D.C.
⤷ Canada: Quebec, British Columbia, Newfoundland. Records from Ontario and Alberta require confirmation.
⤷ Mexico – 1974
Central and South America
⤷ Costa Rica – 2006
⤷ Panamá – 2007
⤷ Colombia – 1975
⤷ Ecuador – 2012
⤷ Peru – 2012
⤷ Chile – ≤2003
⤷ Argentina – 2004
⤷ Brazil – 1991
Oceanic Islands
⤷ Faroe Islands – 1970
⤷ Madeira – 1980
⤷ Azores – 1957
⤷ Canary Islands – 1947
⤷ Tristan da Cunha – 1982
⤷ Raoul Island – 1973
⤷ Chatham Islands – 1976
⤷ Norfolk Island - 2013
⤷ Marion Islands – 1972
⤷ Juan Fernández Islands – 1962
Behavior
The mating behaviour of this species has been particularly well studied, partly to provide taxonomic characters. Mating starts when one individual closely follows the flattened tail of the other. Typically after some minutes the leader turns back and protrudes its sarcobelum, as does its partner shortly afterwards. The partners often form a circle head to tail. Early courtship involves violent biting of the partner, lashing the sarcobelum against the partner, and bursts of tail wagging. This is gradually replaced by more gentle-looking stroking of the sarcobelum across the partner. During courtship, sperm accumulates in the penial caecum. After about 90 minutes the partners orient themselves face-to-face, nibble the base of the partner's raised sarcobelum, and suddenly their penises simultaneously evert. The finger-like penial caecum curves round the back of the partner's sarcobelum, transferring sperm onto it. The penes remain everted for a variable period before the penial lobe and then the penial gland also evert. The latter transfers a secretion onto the partner. This is directly followed by retraction of the penis and then separation.Laboratory experiments suggest that "D. invadens" shows a diurnal rhythm of active locomotion and feeding at night, then inactivity in or below the litter layer during the day; the rhythm is entrained by light. This feeding cycle is accompanied by regular cytological changes in the organs of digestion.
"Deroceras invadens" exhibited the highest crawling speed amongst measurements from 28 species of terrestrial slug and snail.
Habitat
"Deroceras invadens" typically occurs in disturbed sites and is often easiest to find under rubbish. However, this species has also spread to natural habitats such as woodland and grassland. It prefers areas of high humidity and cannot survive temperatures below –7 °C. Its distribution appears restricted by low winter temperatures, which could explain its slow and only partial colonisation of central Europe and its recent range expansion in Sweden following climate amelioration.It can be a significant pest in gardens, greenhouses, pasture, and arable fields. In captivity, slugs eat their own body weight of lettuce in two or three days.
In North Wales, most adults start to lay eggs in autumn and have died by early spring; the species can be found in any season, but it is most abundant in late spring. In New Zealand pastureland, populations fall considerably in summer.
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