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Intestinal helminth communities in the green lizard, Lacerta viridis, from Bulgaria

Published online by Cambridge University Press:  05 June 2009

V. Biserkov  and
A. Kostadinova
V. Biserkov
Affiliation:
Department of Biodiversity, Central Laboratory of General Ecology, Bulgarian Academy of Sciences, 2 Gagarin Street, 1113 Sofia, Bulgaria
A. Kostadinova
Affiliation:
Department of Biodiversity, Central Laboratory of General Ecology, Bulgarian Academy of Sciences, 2 Gagarin Street, 1113 Sofia, Bulgaria
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Abstract

A data set comprising individual host/parasite lists from 100 Lacerta viridis (Reptilia: Lacertidae) belonging to four isolated populations in Bulgaria was studied. A total of seven helminth species was recovered (Leptophallus nigrovenosus, Plagiorchis molini, Oswaldocruzia filiformis, Spauligodon extenuatus, Skrjabinelazia hoffmanni, Physaloptera clausa and Mesocestoides sp.). Lacerta viridis is a new host record for the first five of these species. Communities of intestinal helminths of L. viridis consist of a few species which resulted in a low species richness, abundance and diversity of infracommunities, which exhibit substantial homogeneity among the four samples. A similar pattern of dominance of two nematode species leading to a relatively high community similarity at both infra- and component community levels was observed. While intestinal helminth communities in lizards from ‘marginal’ habitats were dominated by the host generalist, O. filiformis, those in hosts from ‘typical’ habitats were dominated by the lizard specialist S. extenuatus. The results indicate that the characteristics of the host's habitat are important in determining the composition rather than structure of intestinal helminth communities in L. viridis.

Type
Research Papers
Information
Journal of Helminthology , Volume 72 , Issue 3 , September 1998 , pp. 267 - 271
Copyright
Copyright © Cambridge University Press 1998

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References

Aho, J.M. (1990) Helminth communities of amphibians and reptiles: comparative approaches to understanding patterns and processes, pp. 157–190in Esch, G.W., Bush, A.O. & Aho, J.M.(Eds) Parasite communities: patterns and processes. London and New York, Chapman and Hall.CrossRefGoogle Scholar
Arnold, E.N. & Burton, J.A. (1978) A field guide to the reptiles and amphibians of Britain and Europe. 272 pp. London, Collins.Google Scholar
Baev, P. & Penev, L. (1993) BIODIV. Program for calculating biological diversity parameters, similarity, niche overlap, and cluster analysis. Version 4.1. 43 pp. Sofia, Pensoft.Google Scholar
Barker, M.R. (1987) Synopsis of the Nematoda parasitic in amphibians and reptiles. Memorial University of Newfoundland. Occasional Papers in Biology, No. 11. 325 pp.Google Scholar
Bush, A.O., Aho, J.M. & Kennedy, C.R. (1990) Ecological versus phylogenetic determinants of helminth parasite community richness. Evolutionary Ecology 4, 1–20.CrossRefGoogle Scholar
Bush, A.O., Lafferty, K.D., Lotz, J.M. & Shostak, A.W. (1997) Parasitology meets ecology on its own terms: Margolis et al. revisited. Journal of Parasitology 83, 575–583.CrossRefGoogle Scholar
Dobson, A.P., Pacala, S.V., Roughgarden, J.D., Carper, E.R. & Harris, E.A. (1992) The parasites of Anolis lizards in the northern Lesser Antilles. I. Patterns of distribution and abundance. Oecologia 91, 110–117.CrossRefGoogle ScholarPubMed
Georgiev, B., Biserkov, V. & Genov, T. (1986) In toto staining method for cestodes with iron acetocarmine. Helminthologia 23, 279–281.Google Scholar
Krebs, C.J. (1989) Ecological methodology, pp. 293–309. New York, Harper Collins Publishers.Google Scholar
Lewin, J. (1992) Parasites of the sand lizard (Lacerta agilis L.) in Poland. Acta Parasitologica 37, 19–24.Google Scholar
Moravec, F. (1963) Prispevek k poznani helmintofauny nasich plazu. Publications of the Faculty of Sciences, University J.E. Purkyne, Brno 446, 353–395.Google Scholar
Roca, V., Lluch, J. & Navarro, P. (1986) Contribution al conocimiento de la helmintofauna de los herpetos ibericos. I. Parasitos de Lacertidae: Lacerta lepida Daudin, 1802 y Podarcis hispanica Steindachner, 1870. Revista Iberica de Parasitologia 46, 129–136.Google Scholar
Sharpilo, V.P. (1961) [Helminth fauna of Lacerta agilis L. in the Ukraine]. Zbirnik prac' zoologichnogo muzeyu, 30, 85–90 (In Ukrainian.)Google Scholar
Sharpilo, V.P. (1976) [Parasitic worms of the reptilian fauna of the USSR: systematics, chorology, biology.] Naukova Dumka, Kiev, 287 pp. (In Russian.)Google Scholar
Sharpilo, V.P. & Iskova, N.I. (1989) [Fauna Ukrainy, vol. 34 (3), Trematody. Plagiorkhiaty (Plagiorchiata).] Kiev, Naukova Dumka, 277 pp. (In Russian.)Google Scholar
Sokal, R.R. & Rohlf, F.J. (1981) Biometry. The principles and practice of statistics in biological research. Second edition. 859 pp. New York, W.H.Freeman and Co.Google Scholar