BeRMS source details

Clarke, Andrew; Johnston, Nadine M. (2003). Antarctic marine benthic diversity. Oceanography and Marine Biology: an Annual Review. 41: 47-114.
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Clarke, Andrew; Johnston, Nadine M
2003
Antarctic marine benthic diversity
Oceanography and Marine Biology: an Annual Review
41: 47-114
Publication
An unpublished species checklist compiled for background to this paper by the two authors was later used as basis for the Register of Antarctic Marine Species. The review article itself contains no species lists. The journal series is available at https://www.routledge.com but there is no link to the article. The original spreadsheet checklist might be obtainable from the author, accl@bas.ac.uk
Ant'Phipoda Literature database.
Available for editors  PDF available
Species lists have been compiled for all the major groups of Southern Ocean benthic marine invertebrates, eliminating synonymies where possible and providing a subjective estimate of completeness and reliability for each group. Antarctic marine diversity (pelagic and benthic) is relatively high at the phylum and class level, with the gaps mostly comprising minor, meiofaunal or parasitic groups. Most benthic diversity data come from the continental shelves, with relatively few samples from deeper water. Even for the continental shelves, however, sampling is highly patchy with some areas hardly investigated at all. Over 4100 benthic species have been reported from the Southern Ocean, with the most speciose groups being polychaetes, gastropods and amphipods. Comparison with tropical and temperate regions suggest that decapods, bivalves and teleost fishes are poorly represented in the Southern Ocean benthic marine fauna, whereas pycnogonids, echinoderms and many suspension feeding groups are rich and diverse. Some groups that are currently low in diversity were previously well represented in the Antarctic shallow water marine fauna, notably decapods and many fishes. Other groups have undergone marked radiations in the Southern Ocean, including pycnogonids, amphipods, isopods and teleost fishes; in all cases, however, it is only some lineages that have diversified. This indicates that evolutionary questions concerning the origin, diversification or extinction of the Southern Ocean marine fauna will have no single answer; the evolutionary history of each group appears to reflect a different response to the tectonic, climatic and oceanographic changes to which they have been subject through history. The disposition of southern hemisphere continents makes it difficult to assess whether there is a latitudinal cline in shallow-water marine diversity to mirror that known from the northern hemisphere. Within Antarctica, many species appear to have circumpolar distributions, and the long established biogeographical division into continental Antarctic, Antarctic Peninsula and sub-Antarctic regions have not been challenged by recent sampling. For most groups the frequency distribution of species per genus ratios is typical, though none is well described by the predictions from current evolutionary or null models. Where data are available, size spectra indicate that many Southern Ocean taxa are small, a few spectacular examples of gigantism notwithstanding, and species abundance plots are normal. Knowledge of the Southern Ocean benthic marine fauna has reached a stage where we can now ask powerful evolutionary questions, and the development of new molecular techniques provides the mechanism for answering them
Antarctic
Fauna and Flora, Faunistic inventories, Checklists, Catalogues
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2013-01-12 18:30:12Z
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Alcyonidium Lamouroux, 1813 (additional source)
Alcyonidium mytili Dalyell, 1848 accepted as Alcyonidioides mytili (Dalyell, 1848) (additional source)
Amphiblestrum Gray, 1848 (additional source)
Anasca accepted as Flustrina (additional source)
Aricidea (Allia) Strelzov, 1973 accepted as Aricidea (Strelzovia) Aguirrezabalaga, 2012 (additional source)
Beania Johnston, 1840 (additional source)
Beaniidae Canu & Bassler, 1927 (additional source)
Bowerbankia Farre, 1837 accepted as Amathia Lamouroux, 1812 (additional source)
Bryozoa (additional source)
Bugula Oken, 1815 (additional source)
Bugulidae Gray, 1848 (additional source)
Caberea Lamouroux, 1816 (additional source)
Calloporidae Norman, 1903 (additional source)
Cellaria Ellis & Solander, 1786 (additional source)
Cellariidae Fleming, 1828 (additional source)
Celleporella Gray, 1848 (additional source)
Celleporidae Johnston, 1838 (additional source)
Cheilostomatida (additional source)
Conchoderma auritum (Linnaeus, 1767) (additional source)
Cribrilinidae Hincks, 1879 (additional source)
Diastopora Lamouroux, 1821 (additional source)
Electra Lamouroux, 1816 (additional source)
Electridae Stach, 1937 (1851) (additional source)
Escharella Gray, 1848 (additional source)
Escharoides Milne Edwards, 1836 (additional source)
Exochellidae Bassler, 1935 (additional source)
Fenestrulina Jullien, 1888 (additional source)
Figularia Jullien, 1886 (additional source)
Filicrisia d'Orbigny, 1853 (additional source)
Flustridae Fleming, 1828 (additional source)
Golfingia (Golfingia) Lankester, 1885 (basis of record)
Gymnolaemata (additional source)
Hippothoidae Busk, 1859 (additional source)
Limnoriidae White, 1850 (additional source)
Lineidae McIntosh, 1873-1874 (additional source)
Microporellidae Hincks, 1879 (additional source)
Munna Krøyer, 1839 (additional source)
Mycale Gray, 1867 (additional source)
Myxilla Schmidt, 1862 (additional source)
Phascolion (Phascolion) Théel, 1875 (basis of record)
Phascolion (Phascolion) strombus (Montagu, 1804) represented as Phascolion (Phascolion) strombus strombus (Montagu, 1804) (basis of record)
Phidoloporidae Gabb & Horn, 1862 (additional source)
Phorbas Duchassaing & Michelotti, 1864 (additional source)
Rhynchozoon Hincks, 1895 (additional source)
Schizoporellidae Jullien, 1882 (additional source)
Scrupariidae Gray, 1848 (additional source)
Smittina Norman, 1903 (additional source)
Smittinidae Levinsen, 1909 (additional source)
Smittoidea Osburn, 1952 (additional source)
Stomatopora Bronn, 1825 (additional source)
Stomatopora major (Johnston, 1847) accepted as Annectocyma major (Johnston, 1847) (basis of record)
Tricellaria Fleming, 1828 (additional source)
Tubulipora Lamarck, 1816 (additional source)
Umbonulidae Canu, 1904 (additional source)