Hostname: page-component-586b7cd67f-2plfb Total loading time: 0 Render date: 2024-11-30T15:22:39.288Z Has data issue: false hasContentIssue false

Parasite infracommunities of a specialized marine fish species in a compound community dominated by generalist parasites

Published online by Cambridge University Press:  22 May 2009

A.L. Lanfranchi*
Affiliation:
Departamento de Biología, Laboratorio de Parasitología, Facultad de Ciencias Exactas y Naturales, Universidad Nacional de Mar del Plata, Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Funes 3350, (7600)Mar del Plata, Argentina
M.A. Rossin
Affiliation:
Departamento de Biología, Laboratorio de Parasitología, Facultad de Ciencias Exactas y Naturales, Universidad Nacional de Mar del Plata, Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Funes 3350, (7600)Mar del Plata, Argentina
J.T. Timi
Affiliation:
Departamento de Biología, Laboratorio de Parasitología, Facultad de Ciencias Exactas y Naturales, Universidad Nacional de Mar del Plata, Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Funes 3350, (7600)Mar del Plata, Argentina
*
*Fax: +54 223 475-3150 E-mail: [email protected]

Abstract

The structure and composition of parasite communities of Mullus argentinae were analysed under two alternative hypotheses in a sample of 75 specimens caught off Mar del Plata, Argentina (38°27′S, 57°90′W). The first, based on the dominance of trophically transmitted larval parasites of low host-specificity among fish species in the region, predicts that infracommunities will be random subsets of regionally available species. The second, based on previous studies on other mullids, predicts that infracommunities will be dominated by adult digeneans. The parasite fauna of goatfishes was mainly composed of endoparasites, with metacercariae of Prosorhynchus australis accounting for most individual parasites and greatly affecting infracommunity descriptors. Its importance was reinforced by the low number of trophically transmitted larval parasites. Both hypotheses were refuted; parasite communities were not dominated either by trophically transmitted larval parasites of low host-specificity or by adult digeneans. Prosorhynchus australis was the only species displaying any degree of phylogenetic specificity. Therefore, the influence of phylogenetic factors seems to exceed that of ecological ones in determining the observed structure of infracommunities. However, it is precisely host ecology that allows P. australis to become the determinant of infracommunity structure by constraining the acquisition of other parasites. Studies aiming to determine the relative importance of evolutionary and ecological processes as structuring forces of parasite communities should take into account not only the identity and specificity of their component parasites, but also their availability in the compound community.

Type
Research Papers
Copyright
Copyright © Cambridge University Press 2009

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Aguirre, H. & Sánchez, P. (2005) Feeding resource partitioning between Mullus barbatus and M. surmuletus in the Catalan Sea (northwestern Mediterranean). Ciencias Marinas 31, 429439.CrossRefGoogle Scholar
Braicovich, P.E. & Timi, J.T. (2008) Parasites as biological tags for stock discrimination of the Brazilian flathead, Percophis brasiliensis Quoy & Gaimard, 1824, in the South Western Atlantic. Journal of Fish Biology 73, 557571.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, 575583.CrossRefGoogle Scholar
Cousseau, M.B. & Perrotta, R.G. (2004) Peces marinos de Argentina. Biología, distribución, pesca. 167 pp. 2nd edn.Mar del Plata, Argentina, Publicaciones especiales INIDEP.Google Scholar
Cremonte, F. & Sardella, N.H. (1997) The parasitofauna of Scomber japonicus Houttuyn, 1782 (Pisces: Scombridae) in two zones of the Argentine Sea. Fisheries Research 31, 19.CrossRefGoogle Scholar
Etchegoin, J.A., Timi, J.T., Cremonte, F. & Lanfranchi, A.L. (2005) Redescription of Prosorhynchus australis Szidat, 1961 (Digenea: Bucephalidae) parasitizing Conger orbignyanus Valenciennes, 1847 (Pisces: Congridae) from Argentina. Acta Parasitologica 50, 102104.Google Scholar
Ferrer-Castelló, E., Raga, J.A. & Aznar, E.J. (2007) Parasites as fish population tags and pseudoreplication problems: the case of striped red mullet Mullus surmuletus in the Spanish Mediterranean. Journal of Helminthology 81, 169178.Google Scholar
Figus, V., Culurgioni, J., Cortis, M., D'Amico, V. & Canestri Trotti, G. (2004) Digenetic trematodes of Mullus surmuletus (L., 1758) from Gulf of Cagliari, southern Sardinia. Ittiopatologia 1, 4148.Google Scholar
Guégan, J.-F., Lambert, A., Lévêque, C., Combes, C. & Euzet, L. (1992) Can host body size explain the parasite species richness in tropical freshwater fishes? Oecologia 90, 197204.Google Scholar
Holmes, J.C. (1990) Helminth communities in marine fishes. pp. 101130in Esch, G., Bush, A. & Aho, J. (Eds) Parasite communities: patterns and processes. London, Chapman & Hall.CrossRefGoogle Scholar
Laffargue, P., Baudouin, G., Sasal, P., Arnaud, C., Begout Anras, M.L. & Lagardère, F. (2004) Parasitic infection of sole Solea solea by Prosorhynchus spp. metacercariae (Digenea, Bucephalidae) in Atlantic nurseries under mussel cultivation influence. Diseases of Aquatic Organisms 58, 179184.CrossRefGoogle ScholarPubMed
Le Pommelet, E., Bartoli, P. & Silan, P. (1997) Biodiversité des digènes et autres helminthes intestinaux des Rougets: synthèse pour Mullus surmulentus (Linné, 1758) et M. barbatus (L. 1758) dans le basin méditerranéen. Annales des Sciences naturelles, Zoologie Paris, 13th Series 18, 117133.Google Scholar
Luque, J.L., Porrozzi, F. & Alves, D.R. (2002) Community ecology of the metazoan parasites of argentine goatfish, Mullus argentinae (Osteichthyes: Mullidae), from the coastal zone of the state of Rio de Janeiro, Brazil. Revista Brasileira de Parasitolgia Veterinaria 11, 3338.Google Scholar
Luque, J.L., Mouillot, D. & Poulin, R. (2004) Parasite biodiversity and its determinants in coastal marine teleost fishes of Brazil. Parasitology 128, 671682.CrossRefGoogle ScholarPubMed
Magurran, A.E. (1988) Ecological diversity and its measurement. 179 pp. Princeton, Princeton University Press.CrossRefGoogle Scholar
Marcogliese, D.J. (2002) Food webs and the transmission of parasites to marine fish. Parasitology 124, S83S99.CrossRefGoogle ScholarPubMed
Matthews, R.A. (1973) The life-cycle of Prosorhynchus crucibulum (Rudolphi, 1819) Odhner, 1905, and a comparison of its cercaria with that of Prosorhynchus squamatus Odhner, 1905. Parasitology 66, 133164.CrossRefGoogle Scholar
Poulin, R. (2003) The decay of similarity with geographical distance in parasite communities of vertebrate hosts. Journal of Biogeography 30, 16091615.CrossRefGoogle Scholar
Poulin, R. & Morand, S. (1999) Geographical distances and the similarity among parasite communities of conspecific host populations. Parasitology 119, 369374.Google Scholar
Poulin, R. & Morand, S. (2004) Parasite biodiversity. 216 pp. Washington, DC, Smithsonian Institution Press.Google Scholar
Roubal, F.R. (1994) Infection of the kidney of Acanthopagrus australis (Pisces: Sparidae) with Sphaerospora sp. (Myxosporea), Prosorhynchus sp. (Digenea), and cysts of unknown origin. Diseases of Aquatic Organisms 20, 8393.CrossRefGoogle Scholar
Sardella, N.H. & Timi, J.T. (1996) Parasite communities of Merluccius hubbsi from the Argentinian–Uruguayan common fishing zone. Fisheries Reseach 27, 8188.CrossRefGoogle Scholar
Sardella, N.H. & Timi, J.T. (2004) Parasites of Argentine hake in the Argentine Sea: population and infracommunity structure as evidences for host stock discrimination. Journal of Fish Biology 65, 14721488.Google Scholar
Serrano, A., Velasco, F. & Olaso, I. (2003) Polychaete annelids in the diet of demersal fish from the southern shelf of the Bay of Biscay. Journal of the Marine Biological Association of the United Kingdom 83, 619623.CrossRefGoogle Scholar
Stunkard, H.W. (1976) The life cycles, intermediate hosts, and larval stages of Rhipidocotyle transversale Chandler, 1935 and Rhipidocotyle lintoni Hopkins, 1954: life-cycles and systematics of bucephalid trematodes. Biological Bulletin 150, 294317.CrossRefGoogle Scholar
Szidat, L. (1961) Versuch einer Zoogeographie des Süd-Atlantik mit Hilfe von Leitparasiten der Meeresfische. Parasitologische Schriftenreihe 13, 198.Google Scholar
Tanzola, R.D. & Guagliardo, S.E. (2000) Helminth fauna of the Argentine conger, Conger orbignyanus (Pisces: Anguilliformes). Helminthologia 37, 229232.Google Scholar
Timi, J.T. (2003) Parasites of Argentine anchovy in the Southwest Atlantic: latitudinal patterns and their use for discrimination of host populations. Journal of Fish Biology 63, 90107.CrossRefGoogle Scholar
Timi, J.T. (2007) Parasites as biological tags for stock discrimination in marine fish from South American Atlantic waters. Journal of Helminthology 81, 107111.CrossRefGoogle ScholarPubMed
Timi, J.T. & Poulin, R. (2003) Parasite community structure within and across host populations of a marine pelagic fish: how repeatable is it? International Journal for Parasitology 33, 13531362.Google Scholar
Timi, J.T. & Lanfranchi, A.L. (2009) The importance of the compound community on the parasite infracommunity structure in a small benthic fish. Parasitology Research 104, 295302.CrossRefGoogle Scholar
Timi, J.T., Luque, J.L. & Sardella, N.H. (2005) Parasites of Cynoscion guatucupa along South American Atlantic coasts: evidence for stock discrimination. Journal of Fish Biology 67, 16031618.Google Scholar
Timi, J.T., Lanfranchi, A.L., Etchegoin, J.A. & Cremonte, F. (2008) Parasites of the Brazilian sandperch, Pinguipes brasilianus: a tool for stock discrimination in the Argentine Sea. Journal of Fish Biology 72, 13321342.Google Scholar