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Herbivory in small carnivores: benthic hydroids as an example

Published online by Cambridge University Press:  18 December 2008

Josep-Maria Gili*
Affiliation:
Institut de Ciències del Mar (CSIC), Passeig Maritim de la Barceloneta 37–49, 08003 Barcelona, Spain
Alicia Duró
Affiliation:
Institut de Ciències del Mar (CSIC), Passeig Maritim de la Barceloneta 37–49, 08003 Barcelona, Spain
Josep García-Valero
Affiliation:
Facultat de Biología, Universitat de Barcelona, avinguda Diagonal 645, 08028, Spain
Josep M. Gasol
Affiliation:
Institut de Ciències del Mar (CSIC), Passeig Maritim de la Barceloneta 37–49, 08003 Barcelona, Spain
Sergio Rossi
Affiliation:
Institut de Ciència i Technologià Ambientals ICTA, UAB, Campus Cn s/n, Cerdanyola del Vallés 08193, Barcelona, Spain
*
Correspondence should be addressed to: J.-M. Gili, Institut de Ciències del Mar (CSIC), Passeig Maritim de la Barceloneta 37–49, 08003 Barcelona, Spain email: [email protected]

Abstract

Previous evidence has shown that benthic hydroids capture all kinds of available prey and the only known constraint was prey size. Among the prey captured are phytoplankton cells but it is not known whether they are digested and assimilated. To test the hypothesis that benthic hydroids assimilate phytoplankton cells, a series of feeding experiments was carried out with the Mediterranean species Eudendrium racemosum. Ingestion rates and assimilation efficiency were determined by analysing the 14C incorporated from a labelled population of the diatom species Thalassiosira weissflogii. Eudendrium racemosum fed on T. weissflogii, after a period of starvation, and with the diatoms as the sole food item. In the presence of approximately 15,000 diatoms ml−1, Eudendrium fed at rates ranging from 16 to 55 diatoms polyp−1 hour−1. Accumulation of radioactivity in the hydrocaulus and the polyps of the hydroids were observed. A maximum ingestion of 31.6 diatoms per μgC of polyp (i.e. 175 diatoms per polyp) was observed in the experiments. Most of the diatom 14C ingested would have ended up in the Eudendrium tissue (efficiency 94%), and it was expected that a certain percentage would have been respired by the polyps. These data show that Eudendrium feed on phytoplankton, which can satisfy almost 100% of their energy demand when this type of food is sufficiently abundant.

Type
Research Article
Copyright
Copyright © Marine Biological Association of the United Kingdom 2008

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References

REFERENCES

Barangé, M. and Gili, J.M. (1988) Feeding cycles and prey capture in Eudendrium racemosum (Cavolini, 1785). Journal of Experimental Marine Biology and Ecology, 115, 281293.CrossRefGoogle Scholar
Barangé, M., Zabala, M., Riera, T. and Gili, J.M. (1989) A general approach to the in situ energy budget of Eudendrium racemosum (Cnidaria, Hydrozoa) in the Western Mediterranean. Scientia Marina 53, 423427.Google Scholar
Boero, F. (1984) The ecology of marine hydroids and effects of environmental factors: a review. Pubblazione de la Stazione Zoologica di Napoli I: Marine Ecology 5, 93118.CrossRefGoogle Scholar
Boero, F., Bucci, C., Colucci, A.M.R., Gravili, C. and Stabili, L. (in press) Obelia (Cnidaria, Hydrozoa, Campanulariidae) a microphagus, filter feeding medusa. Pubblazione de la Stazione Zoologica di Napoli I: Marine EcologyGoogle Scholar
Bouillon, J. (1995) Classe des Hydrozoaires. In Grassé, P.P. and Doumenc, D. (eds) Traité de Zoologie. Tome III, Fascicle 2: Cnidaires, Cténaires. Paris: Masson, pp. 29416.Google Scholar
Bouillon, J. and Houvenaghel, G. (1970) Histophysiologie de la digestion chez Cladonema radiatum, Dujardin 1843 (Anthomeduse). Pubblazione de la Stazione Zoologica di Napoli 38, 71108.Google Scholar
Buss, L.W. and Jackson, J.B.C. (1981) Planktonic food availability and suspension-feeder abundance: evidence of in situ depletion. Journal of Experimental Marine Biology and Ecology 49, 151161.CrossRefGoogle Scholar
Coma, R., Ribes, M., Gili, J-M. and Zabala, M. (1998) An energetic approach to the study of life-history traits of two modular colonial benthic invertebrates. Marine Ecology Progress Series 162, 89103.CrossRefGoogle Scholar
Coma, R., Ribes, M., Gili, J.M. and Hughes, R.N. (2001) The ultimate opportunists: consumers of seston. Marine Ecology Progress Series 219, 305308.CrossRefGoogle Scholar
Delgado, M., Latasa, M. and Estrada, M. (1992) Variability in the size-fractionated distribution of the phytoplankton across the Catalan front of the north-west Mediterranean. Journal of Plankton Research 14, 753771.CrossRefGoogle Scholar
Fabricius, K., Benayahu, Y. and Genin, A. (1995) Herbivory in asymbiotic soft corals. Science 286, 9092.CrossRefGoogle Scholar
Fabricius, K., Yahel, G. and Genin, A. (1998) In situ depletion of phytoplankton by an azooxanthellate soft coral. Limnology and Oceanography 43, 354356.CrossRefGoogle Scholar
Gili, J.M. and Hughes, R.G. (1995) The ecology of marine benthic hydroids. Oceanography and Marine Biology: an Annual Review 33, 351426.Google Scholar
Gili, J.M., Alvà, V., Pagès, F., Klöser, H. and Arntz, W.E. (1996) Benthic diatoms as the major food source in the sub-Antarctic marine hydroid Silicularia rosea. Polar Biology 16, 507512.CrossRefGoogle Scholar
Gili, J.M., Alvà, V., Coma, R., Orejas, C., Pagès, F., Ribes, M., Zabala, M., Arntz, W., Bouillon, J., Boero, F. and Hughes, R.G. (1997) The impact of small benthic passive suspension feeders in shallow marine ecosystems: the hydroids as an example. Zoologische Verhandelingen 323, 99105.Google Scholar
Gili, J.M. and Coma, R. (1998) Benthic suspension feeders: their paramount role in littoral marine food webs. Trends in Ecology and Evolution 13, 316321.CrossRefGoogle ScholarPubMed
Harris, V.A. (1990) Sessile animals of the sea shore. London: Chapman and Hall, pp. 379.Google Scholar
Herring, T. L., Cohan, C.S., Welnhofer, E.A., Mills, L.R. and Morris, C.E. (1999) F-actin at newly invaginated membrane in neurons: implications for surface area regulation. Journal of Membrane Biology 171, 151169.CrossRefGoogle ScholarPubMed
Lesser, M.P., Witman, J.D. and Sebens, K.P. (1994) Effects of flor and seston availability on scope for growth of benthic suspension feeding invertebrates from the Gulf of Maine. Biological Bulletin. Marine Biological Laboratory, Woods Hole 187, 319335.CrossRefGoogle Scholar
Lunger, P.D. (1963) Fine-structural aspects of digestion in a colonial hydroid. Journal of Ultrastructure Research 9, 362380.CrossRefGoogle Scholar
Marfenin, N.N. (1985) The functioning of the pulsatory–peristaltic type transport system in colonial hydroids. Zhurnal Obshchej Biologii 46, 153164.Google Scholar
Mohlenberg, F. and Riisgård, H.U. (1979) Filtration rates, using a new indirect technique, in thirteen species of suspension-feeding bivalves. Marine Biology 54, 143147.CrossRefGoogle Scholar
Orejas, C., Gili, J.M., Alvà, V. and Arntz, W. (2000) Predatory impact of an epiphytic hydrozoan in an upwelling area in the Bay of Coliumo (Dichato, Chile). Journal of Sea Research 44, 209220.CrossRefGoogle Scholar
Riisgård, H.U. and Larsen, P.S. (2005) Water pumping and analysis of flow burrowing zoobenthos: an overview. Aquatic Ecology 39, 237258.CrossRefGoogle Scholar
Rubenstein, D.I. and Koehl, M.A.R. (1977) The mechanisms of filter feeding: some theoretical considerations. American Naturalist 111, 981994.CrossRefGoogle Scholar
Schierwater, B., Piekos, B. and Buss, L.W. (1992) Hydroid stolonal contractions mediated by contractile vacuoles. Journal of Experimental Biology 162, 121.CrossRefGoogle Scholar
Sebens, K.P. (1987) Coelenterata. In Pandian, T.J. and Vernberg, F.J. (eds) Animal energetics. Volume 1. Protozoa through Insecta. San Diego, CA: Academic Press, Inc, pp. 55120.CrossRefGoogle Scholar
Shimeta, J. and Jumars, P.A. (1991) Physical mechanisms and rates of particle capture by suspension feeders. Oceanography and Marine Biology: an Annual Review 29, 191257.Google Scholar
Widdig, A. and Schlichter, D. (2001) Phytoplankton: a significant trophic source for soft corals? Helgolander Marine Research 55, 198211.CrossRefGoogle Scholar