| Field Guide | MOLLUSCA |
Antarctic soft-shelled
clam Laternula elliptica
Laternula elliptica is found
throughout Antarctica and the Antarctic Peninsula, South Shetland Islands, South
Orkney Islands, South Sandwich Islands, South Georgia Island, Kerguelen Island,
Marion and Prince Edward Islands at depths from 1 to 458+ meters [3,5,10,11,12,14,15]. The shell of L. elliptica can be
up to twelve centimeters in length, and grows to nine centimeters in 12 - 13 years
[1,17]. The shell of L. elliptica is elongated with
coarse growth lines and a brownish edge along the margin [11]. The shell color of L. elliptica is white with a
pinkish or greenish shell covering (periostracum) when alive [12].
Empty
shells of Laternula elliptica are shown here. The primary predator of
unburied L. elliptica is the seastar Odontaster validus; 12% of
its diet can be L. elliptica [2,9]. Predators of
damaged L. elliptica that have been unburied by iceberg scouring include
the seastar Cryptasterias turqueti, the nemertean Parborlasia
corrugatus, the Antarctic whelk Neobuccinum eatoni, and amphipods
[9]. Other predators include the fish Trematomus
bernacchii and the muricid gastropod Trophon longstaffi [16,18].
Here, two
Laternula elliptica have dug themselves into the seafloor so that only
their sparkling greenish siphon pairs show above the gravel bottom.
Laternula elliptica lives buried in gravelly or soft mud
(infaunal) with a large siphon that cannot be fully retracted into its shell;
there is a large gape where the two valves do not close. L. elliptica
filter feeds through these siphons and its food includes benthic diatoms [13]. Its fecal material creates a sediment of organic and
terrigenous mineral particles which enriches the benthic environment [6]. L. elliptica can burrow into the sediment over fifty
centimeters [9]. L. elliptica is found in greatest
density in water shallower than thirty meters [5,10].
Population density ranges up to 140 individuals per square meter [4,5,12].
In shallower depths where its food is more plentiful, the deep burrowing of
L. elliptica keeps it safe from seafloor scouring by pack ice and
icebergs and, secondarily, from predation [5,13]. L.
elliptica can re-burrow itself when exposed and is unusual among burrowing
bivalves because it is capable of surface movement powered by its siphon muscles
and by siphon water jetting [7]. Surface mobility combined
with the ability to re-burrow are adaptations by this deep burrowing bivalve to
periodic natural environmental disturbances like ice scouring [7].
L. elliptica has a protected mode of development where its
embryo develops through larval stages within a protective capsule which
facilitates dispersal in the environment [8].
Laternula elliptica is considered to have been a member of an earlier
Antarctic fauna when the climate was more genial; it is a common fossil found
in beach formations in Antarctica [3,5]. The Laternula genus is widely distributed
in the subtropical and tropical Indo-Pacific. Its deep burrowing lifestyle may
have given a warm-water mollusc sufficient insulation to adjust to a cold-water
habitat [3].
1: Marine Biology 42(2):171-175, 1977;
2: Ecological Monographs 44(1):105-128, 1974; 3: Biogeography and
Ecology in Antarctica. J Van Mieghem and P va Oye, eds. The Hague : W. Junk,
1965. Monographiae Biologicae. Volume 15. pp.333-380; 4: Report of the
Underwater Association 4:91-95, 1969; 5: Holocene Environmental Changes
in Antarctic Coastal Areas : Proceedings of International Workshop held at the
National Institute of Polar Research, Tokyo, October 20-22, 1993. PA Berkman and
Y Yoshida, eds. Tokyo : National Institute of Polar Research, 1994. Memoirs of
National Institute of Polar Research. Special Issue, no. 50 . pp.1-10; 6:
Journal of Experimental Marine Biology and Ecology 171(1):75-90, 1993; 7:
Journal of Molluscan Studies 63(1):109-111, 1997; 8: Journal of
Molluscan Studies 63(2):285-286, 1997; 9: Polar Biology 6(3):139-143,
1986; 10: Antarctic Mollusca : with Special Reference to the Fauna of the
Ross Sea. RK Dell. Wellington, NZ : Royal Society of New Zealand, 1990.
Bulletin 27, Royal Society of New Zealand; 11: Korean Journal of Polar
Research 5(2):15-28, 1994; 12: FAO Species Identification Sheets for
Fishery Purposes : Southern Ocean (Fishing Areas 48, 58 and 88) (CCAMLR
Convention Area). W Fischer & JC Hureau, eds. Rome: Food and Agriculture
Organization of the United Nations, 1985; 13: Antarctic Communities:
Species, Structure, and Survival. B Battaglia, J Valencia, and DWH Walton, eds.
Cambridge: Cambridge University Press, 1997; 14: South African Journal of
Antarctic Research 21(1):45-64, 1991; 15: Polar Biology 20(4):229-247,
1998; 16: Polar Biology 13:291-296, 1993; 17: Ross Sea ecology : Italiantartide Expeditions (1987-
1995). FM Faranda, L Guglielmo, A Ianora, eds. Berlin : Springer, 2000; 18: Polar
Biology 26(3):208-217, 2003
| Text ©Peter Brueggeman. Photographs ©Eva
Philipp & Norbert Wu. Photographs may not be used in any form without the
express written permission of Eva Philipp & Norbert Wu.
Norbert Wu no longer grants permission for uncompensated use of his photos under any circumstances whatsoever;
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