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Spatio-temporal structure of the communities of helminths in the digestive tract of Sciaena umbra L. 1758 (Teleostei)

Published online by Cambridge University Press:  06 April 2009

J. Holmes  and
P. Bartoli
J. Holmes
Affiliation:
Centre de Biologie et d’Ecologie Tropicale et Méditerranéenne, CNRS, URA No. 698, Université de Perpignan, 66860 Perpignan cédex, France Department of Zoology, University of Alberta, Edmonton, Alberta, Canada T6G 2E9
P. Bartoli
Affiliation:
Centre de Biologie et d’Ecologie Tropicale et Méditerranéenne, CNRS, URA No. 698, Université de Perpignan, 66860 Perpignan cédex, France Laboratoire de Biologie Marine et d’Ecologie du Benthos, Faculté des Sciences de Luminy — Case 901, 13288 Marseilles cédex 09, France
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Summary

The helminth community in the digestive tract of the sedentary predatory fish, Sciaena umbra, near the Scandola Nature Reserve, Corsica, consists of 5 species of digeneans. Anoiktostoma coronatum (in the rectum) and Metadena pauli (in the intestine) were found in almost all the fish, and in high numbers; they are considered core species. Distomum aloysiae, Pleorchis polyorchis (both in the intestine), and Stephanostomum bicoronatum (in the rectum) were relatively uncommon, usually found in small numbers, and are considered satellite species. The two core species were very abundant in June, when the size of their populations was strongly correlated with the size of the host fish. At this time, M. pauli was found mainly in the duodenum, but in high populations was spread throughout the intestine (s. strict.). Both species were much less abundant in October, their populations were less dependent on host size, and M. pauli was more limited to the anterior intestine. Pleorchis polyorchis and Distomum aloysiae were more frequent in October, were found predominately in fish with few M. pauli, and were found posterior to M. pauli, suggesting some interactions between these species. Stephano-stomum bicoronatum showed no seasonal patterns, and no apparent interactions with A. coronatum.

Keywords

community structurecompetitionDigeneadigestive tractmicrohabitat
Type
Research Article
Information
Parasitology , Volume 106 , Issue 5 , June 1993 , pp. 519 - 525
Copyright
Copyright © Cambridge University Press 1993

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References

REFERENCES

Aho, J. M., Bush, A. O. & Wolfe, R. (1991). Helminth parasites of bowfin (Amia calva) from South Carolina. Journal of the Helminthological Society of Washington 58, 171–5.Google Scholar
Bartoli, P. (1987). Caractères adaptatifs originaux des digènes intestinaux de Sarpa salpa (Teleostei, Sparidae) at leur interprétation en termes d'évolution. Annales de Parasitologie Humaine et Comparée 62, 542–76.CrossRefGoogle Scholar
Bartoli, P. (1990). Spatiotemporal isolation of intestinal digeneans of Mullus surmuletus. Bulletin de la Société Française de Parasitologie 8 (Suppl. 2), 664 (Abstract).Google Scholar
Bartoli, P. & Gibson, D. I. (1991). On Podocotyle scorpaenae, Poracanthium furcatum and Derogenes latus, three poorly known digenean parasites of western Mediterranean teleosts. Systematic Parasitology 20, 29–46.Google Scholar
Bartoli, P., Gibson, D. I. & Bray, R. A. (1989). The Opecoelidae (Digenea) of sparid fishes of the western Mediterranean. IV. Peracreadium Nicoll, 1909 and Cainocreadium Nicoll, 1909. Systematic Parasitology 14, 53–67.CrossRefGoogle Scholar
Bartoli, P., Gibson, D. I. & Bray, R. A. (1993). The Opecoelidae (Digenea) of sparid fishes of the western Mediterranean. VI. A redescription of Macvicaria mormyri (Stossich, 1885) n. comb, and a key to the Opecoelids from western Mediterranean sparids. Systematic Parasitology (in the Press).Google Scholar
Buchmann, K. (1991). Niche restriction of intestinal helminths from the Baltic flounder (Platichthys flesus). Bulletin of the European Association of Fish Pathologists 11, 86–8.Google Scholar
Bush, A. O. & Holmes, J. C. (1986). Intestinal helminths of lesser scaup ducks: an interactive community. Canadian Journal of Zoology 64, 142–52.Google Scholar
Fischthal, J. H. (1980). Some digenetic trematodes of marine fishes from Israel's Mediterranean coast and their zoogeography, especially those from Red Sea immigrant fishes. Zoologica Scripta 9, 11–23.Google Scholar
Gibson, D. I. & Bray, R. A. (1982). A Study and reorganization of Plagioporus Stafford, 1904 (Digenea: Opecoelidae) and related genera, with special reference to forms from European Atlantic waters. Journal of Natural History 16, 529–59.Google Scholar
Holmes, J. C. (1987). The structure of helminth communities. International Journal for Parasitology 17, 203–8.Google Scholar
Holmes, J. C. (1990). Helminth communities in marine fishes. In Parasite Communities: Patterns and Processes (ed. Esch, G. W., Bush, A. O. & Aho, J. M.) pp. 101–130. London: Chapman and Hall.CrossRefGoogle Scholar
Kennedy, C. R. (1991). The role of interspecific competition in structuring helminth parasite communities. In Second International School: Parasite–Host–Environment (ed. Poljakova-Krusteva, O. et al. ), pp. 185–201. Sofia, Bulgaria: Institute of Parasitology, Bulgarian Academy of Sciences.Google Scholar
Levins, R. (1968). Evolution in Changing Environments: Some Theoretical Explorations. Princeton, N. J.: Princeton University Press.CrossRefGoogle Scholar
Mackenzie, K. & Gibson, D. I. (1970). Ecological studies of some parasites of plaice Pleuronectes platessa L. and flounder Platichthys flesus (L.). In Aspects of Fish Parasitology (ed. Taylor, A. E. R. & Muller, R.). Symposia of the British Society for Parasitology, Vol. 8, pp. 1–42. Oxford: Blackwell Scientific Publications.Google Scholar
Naidjenova, N. N. & Gaevskaya, A. V. (1978). Revision of some trematode species parasites of Black Sea fishes. Biologiya Morya Kiev 45, 49–55.Google Scholar
Papoutsoglou, S. E. (1976). Metazoan parasites of fishes from Saronicos Gulf, Athens, Greece. Thalassographica 1, 69–102.Google Scholar
Sey, O. (1970). Parasitic helminths occurring in Adriatic fishes. Part II (flukes and tapeworms). Acta Adriatica 13, 3–15.Google Scholar
Sogandares-Bernal, F. (1959). Digenetic trematodes of marine fishes from the Gulf of Panama and Bimini, British West Indies. Tulane Studies in Zoology 7, 69–117.Google Scholar
Weldon, C. W. & Slauson, W. L. (1986). The intensity of competition versus its importance: an overlooked distinction. Quarterly Review of Biology 61, 23–44.CrossRefGoogle Scholar
Wilkinson, L. (1990). SYSTAT: The System for Statistics. Evanston, IL.: Systat Inc.Google Scholar
Yamaguti, S. (1958). Systema Helminthum. Vol. I. The Digenetic Trematodes of Vertebrates. New York and London: Interscience Publishers.Google Scholar