Hostname: page-component-586b7cd67f-2plfb Total loading time: 0 Render date: 2024-11-24T14:38:37.091Z Has data issue: false hasContentIssue false

Impacts of gastropods on epiphytic microalgae on the brown macroalga Himantothallus grandifolius

Published online by Cambridge University Press:  15 March 2019

Charles D. Amsler*
Affiliation:
Department of Biology, University of Alabama at Birmingham, 1300 University Blvd., Birmingham, AL 35233-1405, USA
Margaret O. Amsler
Affiliation:
Department of Biology, University of Alabama at Birmingham, 1300 University Blvd., Birmingham, AL 35233-1405, USA
Michelle D. Curtis
Affiliation:
Department of Biology, University of Alabama at Birmingham, 1300 University Blvd., Birmingham, AL 35233-1405, USA
James B. McClintock
Affiliation:
Department of Biology, University of Alabama at Birmingham, 1300 University Blvd., Birmingham, AL 35233-1405, USA
Bill J. Baker
Affiliation:
Department of Chemistry, University of South Florida, 4202 E. Fowler Ave., Tampa, FL 33620, USA

Abstract

Chemically defended benthic macroalgae that dominate shallow, hard bottom communities along the western Antarctic Peninsula support very high densities of mesograzers, particularly amphipods but also small gastropods. Previous studies have demonstrated that the macroalgae and amphipods form a mutualistic relationship. The chemically defended macroalgae provide the amphipods with a refuge from predation while the macroalgae benefit from the amphipods greatly reducing surface fouling by smaller algae. One of the three most important macroalgae in terms of overstory cover, Himantothallus grandifolius, forms huge blades that can carpet the benthos. Field observations suggest that gastropods may be higher in relative abundance in proportion to amphipods on H. grandifolius than on other overstory macroalgae. The present study documents the finding that natural abundances of gastropods on H. grandifolius maintained in mesocosms reduce fouling by microscopic algae, primarily diatoms. However, amphipods are probably also important in keeping the macroalga clean of diatoms in nature. In a smaller scale experiment, three gastropod species were differentially effective at reducing diatom coverage on H. grandifolius. The hypothesis that gastropods benefit from associating with H. grandifolius in potentially gaining a refuge from sea-star predation was also tested but not supported by the experimental results.

Type
Biological Sciences
Copyright
Copyright © Antarctic Science Ltd 2019 

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

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, 10.3354/meps294141.Google 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, 313 pp.Google 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, 10.2216/08-79.1.Google Scholar
Amsler, C.D., McClintock, J.B. & Baker, B.J. 2012. Amphipods exclude filamentous algae from the western Antarctic Peninsula benthos: experimental evidence. Polar Biology, 35, 10.1007/s00300-011-1049-3.Google Scholar
Amsler, C.D., McClintock, J.B. & Baker, B.J. 2014. Chemical mediation of mutualistic interactions between macroalgae and mesograzers structure unique coastal communities along the western Antarctic Peninsula. Journal of Phycology, 50, 10.1111/jpy.12137.Google Scholar
Amsler, M.O., Huang, Y.M., Engl, W., McClintock, J.B. & Amsler, C.D. 2015. Abundance and diversity of gastropods associated with dominant subtidal macroalgae from the western Antarctic Peninsula. Polar Biology, 38, 10.1007/s00300-015-1681-4.Google Scholar
Aumack, C.F., Amsler, C.D., McClintock, J.B. & Baker, B.J. 2010. Chemically mediated resistance to mesoherbivory in finely branched macroalgae along the western Antarctic Peninsula. European Journal of Phycology, 45, 10.1080/09670260903171668.Google Scholar
Aumack, C.F., Amsler, C.D., McClintock, J.B. & Baker, B.J. 2011a. Impacts of mesograzers on epiphyte and endophyte growth associated with chemically defended macroalge from the western Antarctic Peninsula: a mesocosm experiment. Journal of Phycology, 47, 10.1111/j.1529-8817.2010.00927.x.Google Scholar
Aumack, C.F., Amsler, C.D., McClintock, J.B. & Baker, B.J. 2011b. Changes in amphipod densities among macroalgal habitats in day versus night collections along the western Antarctic Peninsula. Marine Biology, 158, 10.1007/s00227-011-1700-0.Google Scholar
Aumack, C.F., Lowe, A.T., Amsler, C.D., Amsler, M.O., McClintock, J.B. & Baker, B.J. 2017. Gut content, fatty acid, and stable isotope analyses reveal dietary sources of macroalgal-associated amphipods along the western Antarctic Peninsula. Polar Biology, 40, 10.1007/s00300-016-2061-4.Google Scholar
Daglio, Y., Sacristán, H., Ansaldo, M. & Rodríguez, M.C. 2018. Benthic diatoms from Potter Cove, 25 de Mayo (King George) Island, Antarctica: mucilage and glucan storage as a C-source for limpets. Polar Science, 15, 10.1016/j.polar.2018.01.004.Google Scholar
De Broyer, C., Koubbi, P., Griffiths, H.J., Raymond, B., d'Udekem d'Acoz, C., van de Putte, A.P., et al. , eds. 2014. Biogeographic atlas of the Southern Ocean. Cambridge: Scientific Committee on Antarctic Research, 498 pp.Google Scholar
Drew, E.A. & Hastings, R.M. 1992. A year-round ecophysiological study of Himantothallus grandifolius (Desmarestiales, Phaeophyta) at Signy Island, Antarctica. Phycologia, 31, 10.2216/i0031-8884-31-3-4-262.1.Google Scholar
Huang, Y.M., Amsler, M.O., McClintock, J.B., Amsler, C.D. & Baker, B.J. 2007. Patterns of gammarid amphipod abundance and species composition associated with dominant subtidal macroalgae along the western Antarctic Peninsula. Polar Biology, 30, 10.1007/s00300-007-0303-1.Google Scholar
Iken, K. 1999. Feeding ecology of the Antarctic herbivorous gastropod Laevilacunaria antarctica Martens. Journal of Experimental Marine Biology and Ecology, 236, 10.1016/S0022-0981(98)00199-3.Google Scholar
McClintock, J.B. 1994. Trophic biology of Antarctic echinoderms. Marine Ecology Progress Series, 111, 191202.Google Scholar
Núñez-Pons, L., Rodríguez-Arias, M., Gómez-Garreta, A., Ribera-Siguán, A. & Avila, C. 2012. Feeding deterrency in Antarctic marine organisms: bioassays with the omnivore amphipod Cheirimedon femoratus. Marine Ecology Progress Series, 462, 10.3354/meps09840.Google Scholar
Peters, A.F. 2003. Molecular identification, taxonomy and distribution of brown algal endophytes, with emphasis on species from Antarctica. Proceedings of the International Seaweed Symposium, 17, 293302.Google Scholar
Picken, G.B. 1979. Growth, production and biomass of the Antarctic gastropod Laevilacunaria antarctica Martens 1885. Journal of Experimental Marine Biology and Ecology, 40, 10.1016/0022-0981(79)90035-2.Google Scholar
Picken, G.B. 1980. The nearshore prostobranch gastropod epifauna of Signy Island, South Orkney Islands. PhD thesis, University of Aberdeen, 257 pp. (Unpublished)Google Scholar
Provasoli, L. 1968. Media and prospects for the cultivation of marine algae. In Watanabe, A. & Hattori, A., eds. Cultures and Collections of Algae, Proceedings of the U.S.-Japan Conference held at Hakone, September 12–15, 1966. Kyoto: Japanese Society of Plant Physiologists, 100 pp.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, 165 pp. (Unpublished)Google Scholar
Steneck, R.S. & Watling, L. 1982. Feeding capabilities and limitation of herbivorous molluscs: a functional group approach. Marine Biology, 68, 10.1007/BF00409596.Google Scholar
Valdivia, N., Pardo, L.M., Macaya, E.C., Huovinen, P. & Gómez, I. In press. Different ecological mechanisms lead to similar grazer controls on the functioning of periphyton Antarctic and sub-Antarctic communities. Progress in Oceanography, 10.1016/j.pocean.2018.01.008.Google Scholar
Wiencke, C. & Amsler, C.D. 2012. Seaweeds and their communities in polar regions. In Wiencke, C. & Bischof, K., eds. Seaweed biology: novel insights into ecophysiology, ecology and utilization. Berlin: Springer, 514 pp.Google Scholar
Wiencke, C., Amsler, C.D. & Clayton, M.N. 2014. Macroalgae. In De Broyer, C., Koubbi, P., Griffiths, H.J., Raymond, B., d'Udekem d'Acoz, C., Van de Putte, A.P., et al. , eds. Biogeographic atlas of the Southern Ocean. Cambridge: Scientific Committee on Antarctic Research, 498 pp.Google Scholar
Zamzow, J.P., Amsler, C.D., McClintock, J.B. & Baker, B.J. 2010. Habitat choice and predator avoidance by Antarctic amphipods: the roles of algal chemistry and morphology. Marine Ecology Progress Series, 400, 10.3354/meps08399.Google Scholar
Zamzow, J.P., Aumack, C.F., Amsler, C.D., McClintock, J.B., Amsler, M.O. & Baker, B.J. 2011. Gut contents and stable isotope analyses of the Antarctic fish, Notothenia coriiceps Richardson, from two macroalgal communities. Antarctic Science, 23, 10.1017/S095410201000091X.Google Scholar
Supplementary material: PDF

Amsler et al. supplementary material

Figures S1-S4

Download Amsler et al. supplementary material(PDF)
PDF 1.2 MB