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Patterns of infracommunity species richness in eels, Anguilla anguilla

Published online by Cambridge University Press:  12 April 2024

J. Norton ,
D. Rollinson  and
J.W. Lewis
J. Norton*
Affiliation:
Wolfson Wellcome Biomedical Laboratories, Department of Zoology, The Natural History Museum, Cromwell Road, London, SW7 5BD, UK, : School of Biological Sciences, Royal Holloway, University of London, Egham, Surrey, TW20 0EX, UK
D. Rollinson
Affiliation:
Wolfson Wellcome Biomedical Laboratories, Department of Zoology, The Natural History Museum, Cromwell Road, London, SW7 5BD, UK, :
J.W. Lewis
Affiliation:
School of Biological Sciences, Royal Holloway, University of London, Egham, Surrey, TW20 0EX, UK
*
*Fax: +44(0) 207 942 5054 Email: jern@nhm.ac.uk
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Abstract

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Between October 1999 and October 2001, a total of 510 European eels Anguilla anguilla were captured in 13 different samples from the rivers Thames (five locations) and Test (one location) in southern England. The relationship between parasite component community species richness (CCR) and maximum infracommunity species richness (ICRmax) compared with that previously observed in bird and mammal hosts. Specifically, the maximum number of parasite species occurring in infracommunities equalled or exceeded half the number of parasite species in the component community at that time, across a wide range of CCR values (2–9 parasite species). Furthermore, the frequency distribution of infracommunity richness (ICR) suggested that the species composition of infracommunities is probably random. These findings suggest that intestinal macroparasite infracommunities in eels are unsaturated and potentially species rich assemblages and, in these respects, share a fundamental similarity with the infracommunities of birds and mammals.

Type
Review Article
Information
Journal of Helminthology , Volume 78 , Issue 2 , June 2004 , pp. 141 - 146
Copyright
Copyright © Cambridge University Press 2004

References

Conneely, J.J. McCarthy, T.K. (1986) Ecological factors influencing the composition of the parasite fauna of the European eel, Anguilla anguilla (L.), in Ireland. Journal of Fish Biology 28: 207–219.CrossRefGoogle Scholar
Cornell, H.V. Lawton, J.H. (1992) Species interactions, local and regional processes, and limits to the richness of ecological communities: a theoretical perspective. Journal of Animal Ecology 61: 1–12.CrossRefGoogle Scholar
Janovy, J. Jr. Clopton, R.E., Clopton, D.A., Snyder, S.D., Efting, A. Krebs, L. (1995) Species density distributions as null models for ecolocically significant interactions of parasite species in an assemblage. Ecological Modelling 77: 189–196.CrossRefGoogle Scholar
Kennedy, C.R. (1990) Helminth communities in freshwater fish: structured communities or stochastic assemblages? pp. 131–156 in Esch, G.W., Bush, A.O. & Aho, J.M. (Eds) Parasite communities: patterns and processes. London, Chapman & Hall.CrossRefGoogle Scholar
Kennedy, C.R. Guégan, J.F. (1994) Regional versus local helminth parasite richness in British freshwater fish: saturated or unsaturated parasite communities? Parasitology 109: 175–185.CrossRefGoogle ScholarPubMed
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
Kennedy, C.R. Hartvigsen, R.A. (2000) Richness and diversity of metazoan communities in brown trout Salmo trutta compared to those of eels Anguilla anguilla in their European heartlands. Parasitology 121: 55–64.CrossRefGoogle ScholarPubMed
Kennedy, C.R., Bush, A.O. Aho, J.M. (1986) Patterns in helminth communities: why are birds and fish different? Parasitology 93: 205–215.CrossRefGoogle ScholarPubMed
Lotz, J.M., Bush, A.O. Font, W.F. (1995) Recruitment-driven, spatially discontinuous communities: a null model for transferred patterns in target communities of intestinal helminths. Journal of Parasitology 81: 12–24.CrossRefGoogle Scholar
Poulin, R. (1996) Richness, nestedness, and randomness in parasite infracommunity structure. Oecologia 105: 545–551.CrossRefGoogle ScholarPubMed
Poulin, R. (1998) Evolutionary ecology of parasites. 212 pp. London, Chapman & Hall.Google Scholar
Poulin, R. (2001) Interactions between species and the structure of helminth communities. Parasitology 122 S3–S11.CrossRefGoogle ScholarPubMed
Poulin, R. Guégan, J.F. (2000) Nestedness, anti-nestedness, and the relationship between prevalence and intensity in ectoparasite assemblages of marine fish: a spatial model of species coexistence. International Journal for Parasitology 30: 1147–1152.CrossRefGoogle Scholar
Price, P.W. Clancy, K.M. (1983) Patterns in the number of helminth parasite species in freshwater fishes. Journal of Parasitology 69: 449–454.CrossRefGoogle Scholar
Rohde, K. (1991) Intra- and interspecific interactions in low density populations in resource-rich habitats. Oikos 60: 91–104.CrossRefGoogle Scholar
Rohde, K. (1994) Niche restriction in parasites: proximate and ultimate causes. Parasitology 109, S69–S84.CrossRefGoogle ScholarPubMed