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Spatial variability of larval parasites harboured by two crab species in an estuarine environment in Argentina

Published online by Cambridge University Press:  08 June 2015

Agustina Mendez Casariego*
Affiliation:
FCEyN, Universidad Nacional de Mar del Plata, CC 1260 Correo Central, B7600WAG, Mar del Plata, Argentina Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Rivadavia 1917, CP C1033AAJ, Ciudad de Buenos Aires, Argentina
Matias Merlo
Affiliation:
FCEyN, Universidad Nacional de Mar del Plata, CC 1260 Correo Central, B7600WAG, Mar del Plata, Argentina Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Rivadavia 1917, CP C1033AAJ, Ciudad de Buenos Aires, Argentina
Jorge Etchegoin
Affiliation:
FCEyN, Universidad Nacional de Mar del Plata, CC 1260 Correo Central, B7600WAG, Mar del Plata, Argentina Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Rivadavia 1917, CP C1033AAJ, Ciudad de Buenos Aires, Argentina
*
Correspondence should be addressed to:A. Mendez Casariego, FCEyN, Universidad Nacional de Mar del Plata, CC 1260 Correo Central, B7600WAG, Mar del Plata, Argentina email: [email protected]

Abstract

Soft bottom intertidals of the Atlantic SW are dominated by the semi-terrestrial crab Neohelice granulata and the grapsid crab Cyrtograpsus angulatus. They are similar in size but C. angulatus is mainly a subtidal species, while N. granulata inhabits the intertidal zones, thus the two species overlap only during high tides in this area. Since these distribution differences between crab species across the Mar Chiquita Coastal lagoon may affect digenean infection success, the objective of this work is to describe the spatial differences in parasite infection levels and their selectivity on the host. To determine possible spatial differences in parasitism levels between sites and crab species across the lagoon, three areas dominated by N. granulata were selected and adult crabs of N. granulata and C. angulatus were collected. Both crab species harboured metacercariae of the digeneans Microphallus szidati and Maritrema bonaerensis (Microphallidae), and cystacanths of the acanthocephalan Profilicollis chasmagnathi (Profilicollidae). Digenean species showed preferences between the two crabs. Maritrema bonaerensis mean intensity was higher in N. granulata than in C. angulatus, while the opposite trend was found for M. szidati and could indicate some level of specificity. These results, nevertheless, depended on the study site. For P. chasmagnathi the highest values of mean intensity depended more on the site than on the crab species. The values found here, compared with previous works from both crab species, suggest that besides the spatial heterogeneity, interspecific competition between parasites could explain the differences observed.

Type
Research Article
Copyright
Copyright © Marine Biological Association of the United Kingdom 2015 

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References

REFERENCES

Alda, P. (2011) Estadios larvales de digeneos parásitos de Heleobia australis (d'Orbigny 1835) en el estuario de Bahía Blanca. Tesis doctoral. Facultad de Ciencias Naturales y Museo. Universidad Nacional de La Plata.Google Scholar
Alda, P., La Sala, L., Marcotegui, P. and Martorelli, S. (2011) Parasites and epibionts of grapsid crabs in Bahia Blanca estuary, Argentina. Crustaceana 84, 559571.Google Scholar
Bortolus, A. and Iribarne, O. (1999) The effect of the SW Atlantic burrowing crab Chasmagnathus granulata on a Spartina salt marsh. Marine Ecology Progress Series 178, 7988.Google Scholar
Boschi, E.E. (2000) Species of Decapod Crustaceans and their distribution in the American marine zoogeographic provinces. Revista de Investigacion y Desarrollo Pesquero (Argentina) 13, 1136.Google Scholar
Botto, F., Mendez Casariego, A., Valiñas, M. and Iribarne, O. (2008) Spatial heterogeneity created by burrowing crabs affects human impact on migratory shorebirds. Estuaries and Coasts 31, 134143.Google Scholar
Bush, A.O., Lafferty, K.D., Lotz, J.M. and Shostak, A.W. (1997) Parasitology meets ecology in its own terms: Margolis et al. revisited. Journal of Parasitology 83, 575583.Google Scholar
Byers, J.E., Blakeslee, A.M.H., Linder, E., Cooper, A.B. and Maguire, T.J. (2008) Controls of spatial variation in the prevalence of trematode parasites infecting a marine snail. Ecology 89, 439451.Google Scholar
Etchegoin, J.A. (2001) Dinámica de los sistemas parasitarios. In Iribarne, O.O. (ed.) Reserva de Biosfera Mar Chiquita: características físicas, biológicas y ecológicas. Editorial Martin: Mar del Plata, pp. 171185.Google Scholar
Etchegoin, J.A. and Martorelli, S.R. (1997) Description of a new species of Maritrema (Digenea: Microphallidae) from Mar Chiquita coastal lagoon (Buenos Aires, Argentina) with notes on its life cycle. Journal of Parasitology 83, 709713.Google Scholar
Etchegoin, J., Merlo, M. and Parietti, M. (2012) The role of the invasive polychaete Ficopomatus enigmaticus (Fauvel, 1923) (Serpulidae) as facilitator of parasite transmission in Mar Chiquita coastal lagoon (Buenos Aires, Argentina). Parasitology 139, 15061512.Google Scholar
Faltýnková, A., Valtonen, E.T. and Karvonen, A. (2008) Spatial and temporal structure of the trematode component community in Valvata macrostoma (Gastropoda, Prosobranchia). Parasitology 135, 16911699.Google Scholar
Fasano, J.L., Hernandez, M.A., Isla, F.I. and Schnack, E.J. (1982) Aspectos evolutivos y ambientales de la laguna Mar Chiquita (provincia de Buenos Aires, Argentina). Oceanologica Acta Número especial 285292.Google Scholar
Fredensborg, B., Mouritsen, K.N. and Poulin, R. (2005) Impact of trematodes on host survival and population density in the intertidal gastropod Zeacumantus subcarinatus. Marine Ecology Progress Series 290, 109117.Google Scholar
Iribarne, O., Bortolus, A. and Botto, F. (1997) Between-habitat differences in burrow characteristics and trophic modes in the southwestern Atlantic burrowing crab Chasmagnathus granulata. Marine Ecology Progress Series 155, 137145.Google Scholar
Iribarne, O., Martinetto, P., Schwindt, E., Botto, F., Bortolus, A. and Garcia Borboroglu, P. (2003) Evidences of habitat displacement between two common soft-bottom SW Atlantic intertidal crabs. Journal of Experimental Marine Biology and Ecology 296, 167182.Google Scholar
Koehler, A. and Poulin, R. (2010) Host partitioning by parasites in an intertidal crustacean community. Journal of Parasitology 96, 862868.Google Scholar
Kuris, A.M. (1991) Guild structure of larval trematodes in molluscan hosts: prevalence, dominance and significance of competition. In Esch, G.W., Bush, A. and Aho, J. (eds) Parasite communities: patterns and processes. London: Chapman and Hall, pp. 69100.Google Scholar
Lei, F. and Poulin, R. (2011) Effects of salinity on multiplication and transmission of an intertidal trematode parasite. Marine Biology 158, 9951003.Google Scholar
Lewis, E., Campbell, J. and Sukhdeo, M. (2002) Parasite behavioural ecology in a field of diverse perspectives. In Lewis, E., Campbell, J. and Sukhdeo, M. (eds) The behavioural ecology of parasites. Wallingford: CABI Publishing, pp. 337346.Google Scholar
Lomovasky, B., Mendez Casariego, A., Brey, T. and Iribarne, O. (2006) The effect of the SW Atlantic burrowing crab Chasmagnathus granulatus on the intertidal razor clam Tagelus plebeius. Journal of Experimental Marine Biology and Ecology 337, 1929.Google Scholar
Martinetto, P., Valiñas, M., Palomo, G. and Iribarne, O. (2007) Negative interactions between two SW Atlantic intertidal crabs in soft-bottom habitats. Marine Biology 151, 14791490.Google Scholar
Martorelli, S.R. (1986) Estudio sistemático y biológico de un digeneo perteneciente a la familia Microphallidae Travassos, 1920. I: Microphallus szidati sp. nov. parásito intestinal de Rallus sanguinolentus sanguinolentus (Aves: Rallidae) e Himantopus melanurus (Aves: Recurvirostridae). Revista Iberica de Parasitologia 46, 373378.Google Scholar
Parietti, M. (2011) Distribución espacial y estabilidad temporal de la comunidad de digeneos larvales que parasitan a Heleobia australis (Mollusca: Cochliopidae) en la laguna Mar Chiquita. Tesis de Licenciatura. Facultad de Ciencias Exactas y Naturales, Universidad Nacional de Mar del Plata: Argentina.Google Scholar
Poulin, R. (2006) Global warming and temperature-mediated increases in cercarial emergence in trematode parasites. Parasitology 132, 143151.Google Scholar
Reta, R., Martos, P., Perillo, G., Piccolo, M. and Ferrante, A. (2001) Características hidrográficas del estuario de la laguna Mar Chiquita. In Iribarne, O.O. (ed.) Reserva de Biósfera Mar Chiquita: características físicas, biológicas y ecológicas. Mar del Plata: Editorial Martín, pp. 3152.Google Scholar
Skirnisson, K., Galaktionov, K.V. and Kozminsky, E.V. (2004) Factors influencing the distribution of digenetic trematode infections in a mudsnail (Hydrobia ventrosa) population inhabiting salt marsh ponds in Iceland. Journal of Parasitology 90, 5059.Google Scholar
Spivak, E., Anger, K., Luppi, T., Bas, C. and Ismael, D. (1994) Distribution and habitat preferences of two grapsid crab species in Mar Chiquita Lagoon (Province of Buenos Aires, Argentina). Helgolander Meeresunters 48, 5978.Google Scholar
Stephens, D.W. and Krebs, J.R. (1986) Foraging theory. Princeton, NJ: Princeton University Press.Google Scholar
Thieltges, D., De Montaudouin, X., Fredensborg, B., Jensen, K., Koprivnikar, J. and Poulin, R. (2008) Production of marine trematode cercariae: a potentially overlooked path of energy flow in benthic systems. Marine Ecology Progress Series 372, 147155.Google Scholar
Thieltges, D.W. and Rick, J. (2006) Effect of temperature on emergence, survival and infectivity of cercariae of the marine trematode Renicola roscovita (Digenea: Renicolidae). Diseases of Aquatic Organisms 73, 6368.Google Scholar
Vizcaino, S.I. (1989) Acanthocephalan parasites of Argentine birds I. Morphological complements to the knowledge of Polymorphus (Prosilicollis) chasmagnathi comb. nov. (Polymorphidae). Studies on Neotropical Fauna and Environment 24, 189192.Google Scholar
Zar, J.H. (1999) Biostatistical analysis. Englewood Cliffs, NJ: Prentice-Hall.Google Scholar