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An evaluation of sponge-associated amphipods from the Antarctic Peninsula

Published online by Cambridge University Press:  02 September 2009

Margaret O. Amsler*
Affiliation:
Department of Biology, University of Alabama at Birmingham, Birmingham, AL 35294-1170, USA
James B. Mcclintock
Affiliation:
Department of Biology, University of Alabama at Birmingham, Birmingham, AL 35294-1170, USA
Charles D. Amsler
Affiliation:
Department of Biology, University of Alabama at Birmingham, Birmingham, AL 35294-1170, USA
Robert A. Angus
Affiliation:
Department of Biology, University of Alabama at Birmingham, Birmingham, AL 35294-1170, USA
Bill J. Baker
Affiliation:
Department of Chemistry, University of South Florida, Tampa, FL 33620, USA

Abstract

Nearshore marine benthic algal communities along the western Antarctic Peninsula harbour extremely high densities of amphipods that probably play important roles in nutrient and energy flow. This study extends our evaluation of the importance of amphipods in the nearshore Antarctic Peninsular benthic communities and focuses on sponge associations. We found a mean density of 542 amphipods per litre (L) sponge for twelve species of ecologically dominant sponges. The highest mean density (1295 amphipods per L sponge) occurred with Dendrilla membranosa Pallas. The amphipod community associated with the 12 sponges was diverse (38 species), with mean species richness values ranging from two to eight species. Mean Shannon diversity indices (H’) ranged from 0.52 to 1.49. Amphipods did not appear to have obligate host relationships. Qualitative gut content analyses indicated that 12 of the 38 amphipod species were found with sponge spicules in their guts. However, only one of the amphipods, Echiniphimedia hodgsoni Walker, had considerable amounts of spicules in the gut. Organic lipophilic and hydrophilic extracts of the twelve sponges were presented in alginate food disks to a sympatric omnivorous amphipod in feeding bioassays and extracts of only two sponges deterred feeding.

Type
Biological Sciences
Copyright
Copyright © Antarctic Science Ltd 2009

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References

Abdo, D.A. 2007. Endofauna differences between two temperate marine sponges (Demospongiae; Haploclerida) from southwest Australia. Marine Biology, 152, 845854.CrossRefGoogle Scholar
Amsler, C.D., McClintock, J.B.Baker, B.J. 2008. Macroalgal chemical defenses in polar marine communities. In Amsler, C.D., ed. Algal chemical ecology. Berlin: Springer, 91103.CrossRefGoogle Scholar
Amsler, C.D., Amsler, M.O., Mcclintock, J.B.Baker, B.J. 2009. Filamentous algal endophytes in macrophytic Antarctic algae: prevalence in hosts and palatability to mesoherbivores. Phycologia, 48.CrossRefGoogle Scholar
Amsler, C.D., Moeller, C.B., McClintock, J.B., Iken, K.B.Baker, B.J. 2000. Chemical defenses against diatom fouling in Antarctic marine sponges. Biofouling, 16, 2945.CrossRefGoogle Scholar
Amsler, C.D., Rowley, R.J., Laur, D.R., Quetin, L.B.Ross, R.M. 1995. Vertical distribution of Antarctic Peninsular macroalgae: cover, biomass, and species composition. Phycologia, 34, 424430.CrossRefGoogle Scholar
Amsler, C.D., Iken, K., McClintock, J.B., Amsler, M.O., Peters, K.J., Hubbard, J.M., Furrow, F.B.Baker, B.J. 2005. Comprehensive evaluation of the palatability and chemical defenses of subtidal macroalgae from the Antarctic Peninsula. Marine Ecology Progress Series, 294, 141159.CrossRefGoogle Scholar
Ankisetty, S., Amsler, C.D., McClintock, J.B.Baker, B.J. 2004. Further membranolide diterpenes from the Antarctic sponge Dendrilla membranosa. Journal of Natural Products, 67, 11721174.CrossRefGoogle ScholarPubMed
Baker, B.J., Kopitzke, R.W., Yoshida, W.Y.McClintock, J.B. 1995. Chemical and ecological studies of the Antarctic sponge Dendrilla membranosa. Journal of Natural Products, 58, 14591462.CrossRefGoogle Scholar
Barnard, J.L.Karaman, G.S. 1991. The families and genera of marine gammaridean Amphipoda (except marine gammaroids). Records of the Australian Museum, 13, 1866.CrossRefGoogle Scholar
Biernbaum, C.K. 1981. Seasonal changes in the amphipod fauna of Microciona prolifera (Ellis and Solander) (Porifera: Demospongia) and associated sponges in a shallow salt-marsh creek. Estuaries, 4, 8596.CrossRefGoogle Scholar
Coleman, C.O. 1989. On the nutrition of two Antarctic Acanthonotozomatidae (Crustacea: Amphipoda). Polar Biology, 9, 287294.CrossRefGoogle Scholar
Coleman, C.O. 1991. Comparative fore-gut morphology of Antarctic Amphipoda (Crustacea) adapted to different food sources. Hydrobiologia, 223, 19.CrossRefGoogle Scholar
Costello, M.J.Myers, A.A. 1987. Amphipod fauna of the sponges Halichondria panicea and Hymeniacidon perleve in Lough Hyne, Ireland. Marine Ecology Progress Series, 41, 115121.CrossRefGoogle Scholar
Crowe, S.E.Thomas, J.D. 2002. Abundance and distribution of commensal amphipods from common marine sponges of southeast Florida. In Escobar-Briones, E. & Alverez, F., eds. Modern approaches to the study of Crustacea. New York: Springer, 105110.CrossRefGoogle Scholar
Daniels, R.A. 1982. Feeding ecology of some fishes of the Antarctic Peninsula. Fisheries Bulletin, 80, 575588.Google Scholar
Dauby, P., Scaliteur, Y.De Broyer, C. 2001. Trophic diversity within the eastern Weddell Sea amphipod community. Hydrobiologia, 443, 6986.CrossRefGoogle Scholar
Dayton, P.K. 1979. Observations on growth, dispersal and population dynamics of some sponges in McMurdo Sound, Antarctica. In Vacelet, J. & Bourney-Esnault, J.N., eds. Biologie des Spongaires, vol. 291. Paris: CNRS, 271282.Google Scholar
Dayton, P.K. 1989. Interdecadal variation in an Antarctic sponge and its predators from oceanographic climate shifts. Science, 245, 14841486.CrossRefGoogle Scholar
Dayton, P.K., Robilliard, G.A., Paine, R.T.Dayton, L.B. 1974. Biological accommodation in the benthic community at McMurdo Sound, Antarctica. Ecological Monographs, 44, 105128.CrossRefGoogle Scholar
De Broyer, C.Jażdżewski, K. 1996. Biodiversity of the Southern Ocean: towards a new synthesis for the Amphipoda (Crustacea). Bollettino del Museo Civico di Storia Naturale Verona, 20, 547568.Google Scholar
De Broyer, C., Lowry, J.K., Jażdżewski, K.Robert, H. 2007. Catalogue of the Gammaridean and Corophiidean Amphipoda of the Southern Ocean, with distribution and ecological data. In De Broyer, C., ed. Census of Antarctic Marine Life: Synopsis of the Amphipoda of the Southern Ocean, vol. 1, part 1. Bulletin de l’Institut Royal des Sciences Naturelles de Belgique, Biologie, 77, supplement 1, 1–325.Google Scholar
De Broyer, C., Scailteur, Y., Chapelle, G.Rauschert, M. 2001. Diversity of epibenthic habitats of gammaridean amphipods in the eastern Weddell Sea. Polar Biology, 24, 744753.CrossRefGoogle Scholar
Delaca, T.E.Lipps, J.H. 1976. Shallow water marine associations, Antarctic Peninsula. Antarctic Journal of the United States, 11, 1, 1220.Google Scholar
Delépine, R., Lamb, I.M.Zimmerman, M.H. 1966. Preliminary report on the marine vegetation of the Antarctic Peninsula. Proceedings of the International Seaweed Symposium, 5, 107116.Google Scholar
Frith, D.W. 1977. A preliminary analysis of the associations of amphipods Microdeutopus damnoniensis (Bate), M. anomalus (Rathke) and Corophium sextoni Crawford with sponges Halichondria panacea (Pallas) and Hymeniacidon perleve (Montagu). Crustaceana, 32, 8118.CrossRefGoogle Scholar
Graeve, M., Dauby, D.Scailteur, Y. 2001. Combined lipid, fatty acid and digestive tract content analyses: a penetrating approach to estimate feeding modes of Antarctic amphipods. Polar Biology, 24, 853862.Google Scholar
Huang, J.P., McClintock, J.B., Amsler, C.D.Huang, Y.M. 2008. Mesofauna associated with the marine sponge Amphimedon viridis: do its physical and chemical attributes provide a prospective refuge from fish predation? Journal of Experimental Marine Biology and Ecology, 362, 95100.CrossRefGoogle Scholar
Huang, Y.M. 2006. An examination of morphological and biological traits of dominant marine plants that regulate patterns of mesograzer communities. PhD thesis, University of Alabama at Birmingham, 142 pp. [Unpublished].Google Scholar
Huang, Y.M., Amsler, M.O., McClintock, J.B., Amsler, C.D.Baker, B.J. 2007. Patterns of gammaridean amphipod abundance and species composition associated with dominant subtidal macroalgae from the western Antarctic Peninsula. Polar Biology, 30, 14171430.CrossRefGoogle Scholar
Iken, K., Quartino, M.L., Barrera-Ora, E., Palermo, J., Wiencke, C.Brey, T. 1998. Trophic relations between macroalgae and herbivores. Berichte zur Polarforschung, 299, 258262.Google Scholar
Jażdżewski, K., Teodorczyk, W., Sicinski, J.Kontek, B. 1991. Amphipod crustaceans as an important component of zoobenthos of the shallow Antarctic sublittoral. Hydrobiologia, 223, 105117.CrossRefGoogle Scholar
Klöser, H., Quartino, M.L.Wiencke, C. 1996. Distribution of macroalgae and macroalgal communities in gradients of physical conditions in Potter Cove, King George Island, Antarctica. Hydrobiologia, 333, 117.CrossRefGoogle Scholar
Koltun, V.M. 1970. Sponges of the Arctic and the Antarctic: a faunistic review. Symposia of the Zoological Society of London, 25, 285297.Google Scholar
Koukouras, A., Rosso, A., Voultsiadou-Koukoura, E., Arvanitidis, C.Stefanidou, D. 1996. Macrofauna associated with sponge species of different morphology. Marine Ecology (P.S.N.Z.), 17, 569582.CrossRefGoogle Scholar
Kunzmann, K. 1996. Die mit ausgewählten Schwämmen (Hexactinellida und Demospongiae) aus dem Weddellmeer, Antarktis, vergesellschaftete fauna. Berichte zur Polarforschung, 210, 193.Google Scholar
Lippert, H., Iken, K., Rachor, E.Wiencke, C. 2001. Macrofauna associated with macroalgae in the Kongsfjord (Spitsbergen). Polar Biology, 24, 512522.Google Scholar
Lockhart, S.J.Jones, C.D. 2008. Biogeographic patterns of benthic invertebrate megafauna on shelf areas with the Southern Ocean Atlantic sector. CCAMLR Science, 15, 167192.Google Scholar
Lörz, A.-N. 2001. Low diversity of spongiculous amphipods observed in the Antarctic autumn. Organisms, Diversity and Evolution, 1, 133138.CrossRefGoogle Scholar
Lörz, A.-N.De Broyer, C. 2004. Description of the ecology of a spongicolous lysianassoid amphipod (Crustacea) from Antarctica. Journal of Natural History, 38, 889899.CrossRefGoogle Scholar
McClintock, J.B., Baker, B.J., Hamman, M., Slattery, M., Kopitzke, R.W.Heine, J. 1994. Tube-foot chemotactic responses of the spongivorous sea star Perknaster fuscus to organic extracts of Antarctic sponges. Journal of Chemical Ecology, 20, 859870.CrossRefGoogle Scholar
McClintock, J.B., Amsler, C.D., Baker, B.J.Van Soest, R. 2005. Ecology of Antarctic marine sponges: an overview. Integrative and Comparative Biology, 45, 359368.CrossRefGoogle ScholarPubMed
Neves, G.Omena, E. 2003. Influence of sponge morphology on the composition of the polychaete fauna of Rocas Atoll, northeast Brazil. Coral Reefs, 22, 123129.CrossRefGoogle Scholar
Oshel, P.E.Steele, D.H. 1985. Amphipod Paramphithoe hystrix: a micropredator on the sponge Haliclona ventilabrum. Marine Ecology Progress Series, 23, 307309.CrossRefGoogle Scholar
Peters, K.J., Amsler, C.D., Mcclintock, J.B., Van Soest, R.W.M., Baker, B.J. In press. Palatability and chemical defenses of sponges from the western Antarctic Peninsula. Marine Ecology Progress Series..Google Scholar
Peterson, C.H.Renaud, P.E. 1989. Analysis of feeding preference experiments. Oecologia, 80, 8286.CrossRefGoogle ScholarPubMed
Poore, A.G.B., Watson, M.J., De Nys, R., Lowry, J.K.Steinberg, P.K. 2000. Patterns of host use amount alga- and sponge-associated amphipods. Marine Ecology Progress Series, 208, 183196.CrossRefGoogle Scholar
Ribeiro, S.M., Omena, E.P.Muricy, G. 2003. Macrofauna associated to Mycale microsignatosa (Porifera: Demospongia) in Rio de Janeiro State, SE Brazil. Estuarine, Coastal and Shelf Science, 57, 952959.CrossRefGoogle Scholar
Richardson, M.G. 1971. The ecology and physiological aspects of Antarctic weed dwelling amphipods (Preliminary report, II). British Antarctic Survey Report, N9/1971 (72)/H, 116. [Unpublished].Google Scholar
Richardson, M.G. 1977. The ecology (including physiological aspects) of selected Antarctic marine invertebrates associated with inshore macrophytes. PhD thesis, University of Durham, 296 pp. [Unpublished].Google Scholar
Skilleter, G.A., Russell, D.B., Degnan, B.M.Garson, M.J. 2005. Living in a potentially toxic environment: comparisons of endofauna in two congeneric sponges from the Great Barrier Reef. Marine Ecology Progress Series, 304, 6775.CrossRefGoogle Scholar
Takeuchi, I.Watanabe, K. 2002. Mobile epiphytic invertebrates inhabiting the brown macroalgae, Desmarestia chordalis, under the coastal fast ice of Lutzow-Holm Bay, East Antarctica. Polar Biology, 25, 624628.CrossRefGoogle Scholar
Thiel, M. 2000. Populations and reproductive biology of two sibling amphipod species from ascidians and sponges. Marine Biology, 137, 661674.CrossRefGoogle Scholar
Thurber, A.R. 2007. Diets of Antarctic sponges: links between the pelagic microbial loop and benthic metazoan food web. Marine Ecology Progress Series, 351, 7789.CrossRefGoogle Scholar
Thurston, M.H. 1972. The crustacean amphipoda of Signy Island, South Orkney Islands. British Antarctic Survey Scientific Report, No. 71, 133 pp.Google Scholar
Thurston, M.H. 1974. Crustacea Amphipoda from Graham Land and the Scotia Arc, collected by Operation Tabarin and the Falkland Islands Dependencies Survey, 1944–1959. British Antarctic Survey Scientific Report, No. 85, 89 pp.Google Scholar
Vader, W. 1984. Notes on Norwegian marine Amphipoda. 8. Amphipods found in association with sponges and tunicates. Fauna Norvegica, A5, 1621.Google Scholar