Hostname: page-component-cd9895bd7-gxg78 Total loading time: 0 Render date: 2024-12-23T12:06:08.707Z Has data issue: false hasContentIssue false
  • English
  • Français

Algal-dwelling Eophliantidae (Amphipoda): description of a new species and key to the world species, with notes on their biogeography

Published online by Cambridge University Press:  09 December 2009

A.N. Lörz ,
N.M. Kilgallen  and
M. Thiel
A.N. Lörz*
Affiliation:
National Institute of Water and Atmospheric Research, Greta Point, Wellington, New Zealand
N.M. Kilgallen
Affiliation:
National Institute of Water and Atmospheric Research, Greta Point, Wellington, New Zealand
M. Thiel
Affiliation:
Universidad Católica del Norte, Larrondo 1281, Coquimbo, Chile Centro de Estudios Avancados en Zonos Aridas (CEAZA), Coquimbo, Chile
*
Correspondence should be addressed to: A.N. Lörz, National Institute of Water and Atmospheric Research, Greta Point, Wellington, New Zealand email: [email protected]
Get access Rights & Permissions [Opens in a new window]

Abstract

Eophliantidae are poorly studied marine algal-dwelling amphipods with a wide distribution. A new species was found to excavate burrows across the main stem of Carpophyllum maschalocarpum (Turner) Grev. in the New Zealand subtidal, and a detailed morphological description of this amphipod is given. Bircenna macayai sp. nov. can be distinguished from other Bircenna species by a combination of the following characters: bilobed coxa 1, merus and carpus of pereopods 5–7 strongly extended posteriorly, crenulate basis of pereopod 7 and smooth posterior margin of epimeron 3, pereopod 7 basis longer than wide. A key to the fourteen world species of Eophliantidae is provided. Taxonomy, evolutionary sequences, functional morphology and biogeography of the Eophliantidae are briefly discussed. New Zealand and Australian shallow waters show the highest species diversity of Eophliantidae, containing both species bearing plesiomorphic and highly derived characters, suggesting that Australasia is an evolutionary centre for this amphipod family.

Keywords

AmphipodaEophliantidaeBircenna macayainew speciesCarpophyllum maschalocarpumfunctional morphologyalgal-dwellingbiogeographyNew ZealandAustralasiaevolutionary centre
Type
Research Article
Information
Journal of the Marine Biological Association of the United Kingdom , Volume 90 , Issue 5 , August 2010 , pp. 1055 - 1063
Copyright
Copyright © Marine Biological Association of the United Kingdom 2009

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

REFERENCES

Adams, N.M. (1997) Common seaweeds of New Zealand. Christchurch: Canterbury University Press, 48 pp. and 48 plates.Google Scholar
Alonso, G. (1980) Anfipodos de la Ria Deseado (Santa Cruz, Argentina) I. Contribucion Cientifica del Centro de Investigacion de Biologia Marina, Argentina 175, 315.Google Scholar
Barnard, J.L. (1972) The marine fauna of New Zealand: algae-living littoral Gammaridea (Crustacea, Amphipoda). New Zealand Department of Scientific and Industrial Research Bulletin 210, 1–216.Google Scholar
Barnard, J.L. (1974) Evolutionary patterns in gammaridean Amphipoda. Crustaceana 27, 137–146.CrossRefGoogle Scholar
Barnard, J.L. and Karaman, G.S. (1991) The families and genera of marine gammaridean Amphipoda (except marine gammaroids). Records of the Australian Museum Supplement 13, 1–866.CrossRefGoogle Scholar
Beckley, L.E and Branch, G.M. (1992) A quantitative scuba-diving survey of the sublittoral macrobenthos at subantarctic Marion Island. Polar Biology 11, 553–565.CrossRefGoogle Scholar
Chevreux, E. (1906) Crustacés amphipodes. Expédition Antarctiques francaise (1903–1905). Sciences Naturelles: Documents Scientifiques 1–100.Google Scholar
Chilton, C. (1884) Notes on a few Australian Edriophthalmata 9, 1035–1044, Pl. 1046, 1047.Google Scholar
Choat, J.H. and Clements, K.D. (1993) Daily feeding rates in herbivorous labroid fishes. Marine Biology 117, 205–211.CrossRefGoogle Scholar
Coleman, C.O. (2003) ‘Digital inking’: how to make perfect line drawings on computers. Organism, Diversity and Evolution, Electronic Supplement, http://senckenberg.de/odes/03-14.htm 14, 1–14.Google Scholar
De Broyer, C., Lowry, J.K., Jażdżewski, K. and Robert, H. (2007) Synopsis of the Amphipoda of the Southern Ocean. Volume 1, Part 1. Catalogue of the Gammaridean and Corophiidean Amphipoda (Crustacea) of the Southern Ocean, with distribution and ecological data. Bulletin de l'Institute Royal des Sciences Naturelles de Belgique 77 Supplement 1, 1–325.Google Scholar
Donald, K.M., Kennedy, M. and Spencer, H.G. (2005) Cladogenesis as the result of long-distance rafting events in South Pacific topshells (Gastropoda, Trochidae). Evolution 59, 1701–1711.Google ScholarPubMed
Fraser, C.I., Nikula, R., Spencer, H.G. and Waters, J.M. (2009) Kelp genes reveal effects of subantarctic sea ice during the Last Glacial Maximum. Proceedings of the National Academy of Sciences USA 106, 3249–3253.CrossRefGoogle ScholarPubMed
Gonzalez, E.R., Haye, P.A., Balanda, M.J. and Thiel, M. (2008) Systematic list of species of peracarids from Chile (Crustacea, Eumalacostraca). Gayana 72, 157–177.Google Scholar
Heads, M. (2005) Towards a panbiogeography of the seas. Biological Journal of the Linnean Society 84, 675–723.CrossRefGoogle Scholar
Helmuth, B., Veit, R.R. and Holberton, R. (1994) Long-distance dispersal of a subantarctic brooding bivalve (Gaimardia trapesina) by kelp-rafting. Marine Biology 120, 421–426.CrossRefGoogle Scholar
Kingsford, M.J. (1992) Drift algae and small fish in coastal waters of northeastern New Zealand. Marine Ecology Progress Series 80, 41–55.CrossRefGoogle Scholar
Kreibhom de Paternoster, I. and Escofet, A. (1976) La fauna de anfipodos asociada a los bosques de Macrocystis pyrifera en El Chubut: Amphithoe femorata (Krøyer) (Amphithoidae) y Bircenna fulva Chilton (Eophliantidae). Physis 35, 77–91.Google Scholar
Myers, A.A. (1985) Shallow-water, coral reef and mangrove Amphipoda (Gammaridea) of Fiji. Records of the Australian Museum Supplement 5, 1–143.CrossRefGoogle Scholar
Stephensen, K. (1933) Amphipoda. In The Galathea Expedition 1928, Volume 79. Copenhagen: C.A. Reitzels Forlag, pp. 28–31.Google Scholar
Taylor, R.B. (1998) Seasonal variation in assemblages of mobile epifauna inhabiting three subtidal brown seaweeds in northeastern New Zealand. Hydrobiologia 361, 25–35.CrossRefGoogle Scholar
Taylor, R. and Cole, R. (1994) Mobile epifauna on subtidal brown seaweeds in northeastern New Zealand. Marine Ecology Progress Series 115, 271–282.CrossRefGoogle Scholar
Thiel, M. (2002) The zoogeography of algae-associated peracarids along the Pacific coast of Chile. Journal of Biogeography 29, 999–1008.CrossRefGoogle Scholar
Thiel, M. and Haye, P.A. (2006) The ecology of rafting in the marine environment—III. Biogeographical and evolutionary consequences. Oceanography and Marine Biology: an Annual Review 44, 323–429.Google Scholar
Waters, J.M. and Roy, M.S. (2004) Out of Africa: the slow train to Australasia. Systems Biology 53, 18–24.CrossRefGoogle ScholarPubMed
Waters, J.M. (2008) Marine biogeographic disjunction in temperate Australia: historical landbridge, contemporary currents, or both? Diversity and Distributions 14, 692–700.CrossRefGoogle Scholar
Watling, L. (1989) Classification system for crustacean setae based on the homology concept. In Felgenhauer, B.E., Watling, L. and Thistle, A.B. (eds) Functional morphology of feeding and grooming in Crustacea. Rotterdam: A.A. Balkema, p. 214.Google Scholar