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Composition and structure of helminth communities in eels Anguilla anguilla from Italian coastal lagoons

Published online by Cambridge University Press:  05 June 2009

C.R. Kennedy ,
D. Di Cave ,
F. Berrilli  and
P. Orecchia
C.R. Kennedy
Affiliation:
Department of Biological Sciences, Hatherly Laboratories, University of Exeter, Prince of Wales Road, Exeter, EX4 4PS, UK
D. Di Cave
Affiliation:
Dipartimento di Sanità Pubblica e Biologia Cellulare, Università di Roma “Tor Vergata”, Via di Tor Vergata 135, 00133 Roma, Italy
F. Berrilli
Affiliation:
Dipartimento di Sanità Pubblica e Biologia Cellulare, Università di Roma “Tor Vergata”, Via di Tor Vergata 135, 00133 Roma, Italy
P. Orecchia
Affiliation:
Dipartimento di Sanità Pubblica e Biologia Cellulare, Università di Roma “Tor Vergata”, Via di Tor Vergata 135, 00133 Roma, Italy
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Abstract

The composition and diversity of total and intestinal helminth component and infracommunities were determined in eels Anguilla anguilla from four shallow coastal lagoons near Rome. The lagoons differed principally in respect of their salinity. Only Lake Burano still received an input of freshwater, and both freshwater and marine helminth species were found in eels. In the other three lagoons all helminth species were marine or euryhaline and communities were dominated by digeneans. At component community level these three lagoons were far more similar to each other than to Lake Burano, but this distinction almost disappeared at infracommunity level. Species richness and diversity declined with increasing salinity at component community level but not at infracommunity level. Despite the changes and differences in helminth community composition, intestinal helminth infracommunity structure was very similar in all four lagoons and to that in eels from freshwater localities in Britain. The findings thus provide further and unexpected support for the view that some factor(s) other than supply side ones must be operating to produce the fundamental structural similarity in helminth communities in eels.

Type
Research Papers
Information
Journal of Helminthology , Volume 71 , Issue 1 , March 1997 , pp. 35 - 40
Copyright
Copyright © Cambridge University Press 1997

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References

Crane, J.S. & Eversole, A.G. (1981) Helminth parasites of American eels from brackish water. Proceedings of the Annual Conference of the South East Association of Fish and Wildlife Agencies 35, 355–364.Google Scholar
Dawes, B. (1946) The Trematoda. Cambridge, University Press.Google Scholar
Esch, G.W., Kennedy, C.R., Bush, A.O. & Aho, J.M. (1988) Patterns in helminth communities in freshwater fish in Great Britain: alternative strategies for colonisation. Parasitology 96, 519–532.CrossRefGoogle Scholar
Holmes, J.C. & Price, P.W. (1986) Communities of parasites, pp. 187–213in Kikkawa, J. & Anderson, D.J. (Eds) Community ecology: pattern & process. Oxford, Blackwell Scientific Publications.Google Scholar
Kazic, D., Ubelaker, J.F. & Canovic, M. (1982) The endohelminths of eel (Anguilla anguilla L., 1758) of Lake Skadar and some tributaries. Ichthyologia 14, 41–53.Google Scholar
Kennedy, C.R. (1985) Site segregation by species of Acanthocephala in fish, with special reference to eels, Anguilla anguilla. Parasitology 90, 375–390.CrossRefGoogle Scholar
Kennedy, C.R. (1990) Helminth communities in fresh water fish: structured communities or stochastic assemblages? pp. 131–156in Esch, G.W., Bush, A.O. & Aho, J.M. (Eds) Parasite communities: patterns and processes. London, Chapman and Hall.CrossRefGoogle Scholar
Kennedy, C.R. (1993) The dynamics of intestinal helminth communities in eels Anguilla anguilla in a small stream:long term changes in richness and structure. Parasitology 107, 71–78.CrossRefGoogle Scholar
Kennedy, C.R. (1995) Richness and diversity of helminth communities in tropical eels Anguilla reinhardtii in Queensland, Australia. Parasitology 111, 233–245.CrossRefGoogle Scholar
Kennedy, C.R. & Guégan, J.-F. (1996) The number of niches in intestinal helminth communities of Anguilla anguilla: are there enough spaces for parasites? Parasitology 113, 293–302.CrossRefGoogle Scholar
Køie, M. (1988 a) Parasites in European eel Anguilla anguilla (L.) from Danish freshwater, brackish and marine localities. Ophelia 29, 93–118.CrossRefGoogle Scholar
Køie, M. (1988 b) Parasites in eels, Anguilla anguilla (L.)from eutrophic Lake Esrum (Denmark). Acta Parasitologica Polonica 33 89–100.Google Scholar
Magurran, A.E. (1988) Ecological diversity and its measurement.London, Croom Helm Ltd.CrossRefGoogle Scholar
Margolis, L., Esch, G.W., Holmes, J.C., Kuris, A.M. & Schad, G.A. (1982) The use of ecological terms in parasitology (Report of an ad hoc committee of the American Society of Parasitologists). Journal of Parasitology 68, 131–133.CrossRefGoogle Scholar
Moravec, F. (1985) Occurrence of endoparasitic helminths in eels (Anguilla anguilla (L.)) from the Macha Lake fishpond system, Czechoslovakia. Folia Parasitologica 32, 113–125.Google Scholar
Orecchia, P., Bianchini, M., Catalini, N., Cataudella, S. & Paggi, L. (1987) Parasitological study of a population from of Tiber River eels (Anguilla anguilla). Parassitologia 29, 37–47.Google ScholarPubMed
Seyda, M. (1973) Parasites of eel Anguilla anguilla (L.) from the Szczecin Firth and adjacent waters. Acta Ichthyologia et Piscatoria 3, 67–76.CrossRefGoogle Scholar
Tesch, F.-W. (1977) The eel. London, Chapman & Hall.CrossRefGoogle Scholar