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Further support for thermal ecosystem engineering by wandering albatross

Published online by Cambridge University Press:  17 September 2015

Tanya M. Haupt ,
Brent J. Sinclair ,
Justine D. Shaw  and
Steven L. Chown
Tanya M. Haupt
Affiliation:
Centre for Invasion Biology, Department of Botany and Zoology, Stellenbosch University, Private Bag X1, Matieland 7602, South Africa Current address: Department of Environmental Affairs, Oceans and Coasts Branch, Marine Biodiversity and Ecosystem Research, Private Bag X2, Roggebaai 8012, South Africa
Brent J. Sinclair
Affiliation:
Department of Biology, University of Western Ontario, London, Ontario N6A 5B7, Canada
Justine D. Shaw
Affiliation:
School of Biological Sciences, University of Queensland, St. Lucia, QLD 4072, Australia Terrestrial and Nearshore Ecosystems, Australian Antarctic Division, Kingston, TAS 7050, Australia
Steven L. Chown*
Affiliation:
School of Biological Sciences, Monash University, VIC 3800, Australia
*
*corresponding author: steven.chown@monash.edu
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Abstract

On sub-Antarctic Marion Island, wandering albatross (Diomedea exulans) nests support high abundances of tineid moth, Pringleophaga marioni, caterpillars. Previous work proposed that the birds serve as thermal ecosystem engineers by elevating nest temperatures relative to ambient, thereby promoting growth and survival of the caterpillars. However, only 17 days of temperature data were presented previously, despite year-long nest occupation by birds. Previous sampling was also restricted to old and recently failed nests, though nests from which chicks have recently fledged are key to understanding how the engineering effect is realized. Here we build on previous work by providing nest temperature data for a full year and by sampling all three nest types. For the full duration of nest occupancy, temperatures within occupied nests are significantly higher, consistently by c. 7°C, than those in surrounding soils and abandoned nests, declining noticeably when chicks fledge. Caterpillar abundance is significantly higher in new nests compared to nests from which chicks have fledged, which in turn have higher caterpillar abundances than old nests. Combined with recent information on the life history of P. marioni, our data suggest that caterpillars are incidentally added to the nests during nest construction, and subsequently benefit from an engineering effect.

Keywords

abundancedetritivoredevelopmentmicroclimatesoil biologysurvivalthermal biology
Type
Biological Sciences
Information
Antarctic Science , Volume 28 , Supplement 1 , February 2016 , pp. 35 - 43
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Copyright
© Antarctic Science Ltd 2015 

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References

Bancroft, W.J., Garkaklis, M.J. & Roberts, J.D. 2005. Burrow building in seabird colonies: a soil-forming process in island ecosystems. Pedobiologia, 49, 149–165.CrossRefGoogle Scholar
Barendse, J. & Chown, S.L. 2001. Abundance and seasonality of mid-altitude fellfield arthropods from Marion Island. Polar Biology, 24, 73–82.CrossRefGoogle Scholar
Burger, A.E. 1978. Terrestrial invertebrates: a food resource for birds at Marion Island. South African Journal of Antarctic Research, 8, 87–99.Google Scholar
Chown, S.L. & Froneman, P.W. 2008. The Prince Edward Islands. Land-sea interactions in a changing ecosystem. Stellenbosch: Sun Press, 450 pp.CrossRefGoogle Scholar
Chown, S.L., McGeoch, M.A. & Marshall, D.J. 2002. Diversity and conservation of invertebrates on the sub-Antarctic Prince Edward Islands. African Entomology, 10, 67–82.Google Scholar
Cloern, J.E., Foster, S.Q. & Kleckner, A.E. 2014. Phytoplankton primary production in the world’s estuarine-coastal ecosystems. Biogeosciences, 11, 2477–2501.Google Scholar
Colinet, H., Sinclair, B.J., Vernon, P. & Renault, D. 2015. Insects in fluctuating thermal environments. Annual Review of Entomology, 60, 123–140.Google Scholar
Crafford, J.E. & Scholtz, C.H. 1986. Impact of Embryonopsis halticella Eaton larvae (Lepidoptera: Yponomeutidae) feeding in Marion Island tussock grassland. Polar Biology, 6, 191–196.CrossRefGoogle Scholar
Crafford, J.E. & Scholtz, C.H. 1987. Quantitative differences between the insect faunas of sub-Antarctic Marion and Prince Edward Islands: a result of human intervention? Biological Conservation, 40, 255–262.CrossRefGoogle Scholar
Crafford, J.E., Scholtz, C.H. & Chown, S.L. 1986. The insects of sub-Antarctic Marion and Prince Edward Islands with a bibliography of entomology of the Kerguelen Biogeographical Province. South African Journal of Antarctic Research, 16, 42–84.Google Scholar
Crawford, R.J.M. & Cooper, J. 2003. Conserving surface-nesting seabirds at the Prince Edward Islands: the roles of research, monitoring and legislation. African Journal of Marine Science, 25, 415–426.Google Scholar
Crawley, M.J. 2012. The R book, 2nd ed. Chichester: John Wiley & Sons, 1076 pp.CrossRefGoogle Scholar
Erskine, P.D., Bergstrom, D.M., Schmidt, S., Stewart, G.R., Tweedie, C.E. & Shaw, J.D. 1998. Subantarctic Macquarie Island: a model ecosystem for studying animal-derived nitrogen sources using 15N natural abundance. Oecologia, 117, 187–193.Google Scholar
Gabriel, A.G.A., Chown, S.L., Barendse, J., Marshall, D.J., Mercer, R.D., Pugh, P.J.A. & Smith, V.R. 2001. Biological invasions of Southern Ocean islands: the Collembola of Marion Island as a test of generalities. Ecography, 24, 421–430.Google Scholar
Gaston, K.J., Blackburn, T.M. & Gregory, R.D. 1999. Does variation in census area confound density comparisons? Journal of Applied Ecology, 36, 191–204.Google Scholar
Gremmen, N.J.M. 1982. The vegetation of the subantarctic islands Marion and Prince Edward. The Hague: W. Junk, 164 pp.Google Scholar
Hänel, C. 1999. The distribution and abundance of macro-invertebrates in the major vegetation communities of Marion Island and the impact of alien species. MSc thesis, University of Pretoria, South Africa, 121 pp. [Unpublished].Google Scholar
Haupt, T.M., Crafford, J.E. & Chown, S.L. 2014a. Solving the puzzle of Pringleophaga – threatened, keystone detritivores in the sub-Antarctic. Insect Conservation and Diversity, 7, 308–313.Google Scholar
Haupt, T.M., Sinclair, B.J. & Chown, S.L. 2014b. Chemosensory and thermal cue responses in the sub-Antarctic moth Pringleophaga marioni: do caterpillars choose wandering albatross nest proxies? Polar Biology, 37, 555–563.CrossRefGoogle Scholar
Jackman, S. 2014. Package ‘pscl’. Available at: https://cran.r-project.org/web/packages/pscl/pscl.pdf.Google Scholar
Jones, M.G.W. & Ryan, P.G. 2010. Evidence of mouse attacks on albatross chicks on sub-Antarctic Marion Island. Antarctic Science, 22, 39–42.Google Scholar
Joly, Y., Frenot, Y. & Vernon, P. 1987. Environmental modifications of a subantarctic peat-bog by the wandering albatross (Diomedea exulans): a preliminary study. Polar Biology, 8, 61–72.CrossRefGoogle Scholar
Klok, C.J. & Chown, S.L. 1997. Critical thermal limits, temperature tolerance and water balance of a sub-Antarctic caterpillar, Pringleophaga marioni (Lepidoptera: Tineidae). Journal of Insect Physiology, 43, 685–694.Google Scholar
Moravcová, A., Beyens, L. & van de Vijver, B. 2010. Diatom communities in soils influenced by the wandering albatross (Diomedea exulans). Polar Biology, 33, 241–255.CrossRefGoogle Scholar
Polis, G.A., Anderson, W.B. & Holt, R.D. 1997. Toward an integration of landscape and food web ecology: the dynamics of spatially subsidized food webs. Annual Review of Ecology and Systematics, 28, 289–316.Google Scholar
Polis, G.A., Sànchez-Piñero, F., Stapp, P.T., Anderson, W.B. & Rose, M.D. 2004. Trophic flows from water to land: marine input affects food webs of islands and coastal ecosystems worldwide. In Polis, G.A., Power, M.E. & Huxe, G.R., eds. Food webs at the landscape level. Chicago: University of Chicago Press, 200–216.Google Scholar
R Development Core Team. 2013. R: a language and environment for statistical computing. Vienna: R Foundation for Statistical Computing, Available at: http://www.R-project.org, accessed 3 April 2013.Google Scholar
Ryan, P.G. & Bester, M.N. 2008. Pelagic predators. In Chown, S.L. & Froneman, P.W., eds. The Prince Edward Islands. Land-sea interactions in a changing ecosystem. Stellenbosch: Sun Press, 121–164.Google Scholar
Sànchez-Piñero, F. & Polis, G.A. 2000. Bottom-up dynamics of allochthonous input: direct and indirect effects of seabirds on islands. Ecology, 81, 3117–3132.Google Scholar
Sinclair, B.J. & Chown, S.L. 2005. Deleterious effects of repeated cold exposure in a freeze-tolerant sub-Antarctic caterpillar. Journal of Experimental Biology, 208, 869–879.CrossRefGoogle Scholar
Sinclair, B.J. & Chown, S.L. 2006. Caterpillars benefit from thermal ecosystem engineering by wandering albatrosses on sub-Antarctic Marion Island. Biology Letters, 2, 51–54.Google Scholar
Smith, V.R. 1978. Animal-plant-soil nutrient relationships on Marion Island (sub-Antarctic). Oecologica, 32, 239–253.CrossRefGoogle Scholar
Smith, V.R. 2008. Terrestrial and freshwater primary production and nutrient cycling. In Chown, S.L. & Froneman, P.W., eds. The Prince Edward Islands. Land-sea interactions in a changing ecosystem. Stellenbosch: Sun Press, 181–214.CrossRefGoogle Scholar
Smith, V.R., Avenant, N.L. & Chown, S.L. 2002. The diet and impact of house mice on a sub-Antarctic island. Polar Biology, 25, 703–715.Google Scholar
Vincke, S., van de Vijver, B., Ledeganck, P., Nijs, I. & Beyens, L. 2007. Testacean communities in perturbed soils: the influence of the wandering albatross. Polar Biology, 30, 395–406.Google Scholar
Warham, J. 1990. The petrels, their ecology and breeding systems. London: Academic Press, 452 pp.Google Scholar
Wright, J.P. & Jones, C.G. 2006. The concept of organisms as ecosystem engineers ten years on: progress, limitations, and challenges. BioScience, 56, 203–209.Google Scholar
Zuur, A.F., Ieno, E.N., Walker, N., Saveliev, A.A. & Smith, G.M. 2009. Mixed effects models and extensions in Ecology with R. New York, NY: Springer, 600 pp.Google Scholar
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Haupt supplementary material

Figure S1 and Table S1-S2

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