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The role of the invasive polychaete Ficopomatus enigmaticus (Fauvel, 1923) (Serpulidae) as facilitator of parasite transmission in Mar Chiquita coastal lagoon (Buenos Aires, Argentina)

Published online by Cambridge University Press:  19 July 2012

J. A. ETCHEGOIN*
Affiliation:
Laboratorio de Parasitología, IIMyC, Facultad de Ciencias Exactas y Naturales, Universidad Nacional de Mar del Plata/CONICET, Funes 3350, 7600 Mar del Plata, Argentina
M. J. MERLO
Affiliation:
Laboratorio de Parasitología, IIMyC, Facultad de Ciencias Exactas y Naturales, Universidad Nacional de Mar del Plata/CONICET, Funes 3350, 7600 Mar del Plata, Argentina
M. PARIETTI
Affiliation:
Laboratorio de Parasitología, IIMyC, Facultad de Ciencias Exactas y Naturales, Universidad Nacional de Mar del Plata/CONICET, Funes 3350, 7600 Mar del Plata, Argentina
*
*Corresponding author: Tel: +54 223 4752426. Fax: +54 223 4753150. E-mail: [email protected]

Summary

In Mar Chiquita coastal lagoon (Argentina), the reefs of the invasive polychaete Ficopomatus enigmaticus (Serpulidae) serve as concentration areas for invertebrates and vertebrates and as potential foci of parasite transmission (mainly digeneans). To analyse the role of F. enigmaticus as facilitator of parasite transmission, and to evaluate the influence of the habitats selected by 2 species of cochliopid snails (Heleobia conexa and Heleobia australis), on the richness and on the prevalence of the digenean assemblages that parasitize them, 1945 snails were collected from 2 sampling sites. The comparisons between larval digenean communities parasitizing both snail hosts revealed significant differences related to the overall prevalence and the prevalence contributed by birds in the snails collected from reefs. These results support the idea that the reefs may increase the number of links between intermediate and definitive hosts of digeneans, facilitating parasite transmission only when the aggregates of F. enigmaticus become the unique habitat of the snail host. This first report of an exotic species acting as facilitator of parasite transmission in an estuarine area highlights the importance of analysing the effects of the assimilation process of exotic species by recently colonized environments (including the possible effects on parasite transmission).

Type
Research Article
Copyright
Copyright © Cambridge University Press 2012

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References

REFERENCES

Botto, F., Iribarne, O. O. and Martínez, M. M. (1998). The effect of migratory shorebirds on the benthic species of three southwestern Atlantic Argentinean Estuaries. Estuaries 21, 700709. doi:10.2307/1353274.CrossRefGoogle Scholar
Brooks, D. R. and Hoberg, E. P. (2007). How will global climate change affect parasite-host assemblages? Trends in Parasitology 23, 571574. doi: 10.1016/j.pt.2007.08.016.CrossRefGoogle ScholarPubMed
Bruschetti, M., Luppi, T., Fanjul, E., Rosenthal, A. and Iribarne, O. (2008). Grazing effect of the invasive reef-forming polychaete Ficopomatus enigmaticus (Fauvel) on phytoplankton biomass in a SW Atlantic coastal lagoon. Journal of Experimental Marine Biology and Ecology 354, 212219. doi:10.1016/j.jembe.2007.11.009.CrossRefGoogle Scholar
Bruschetti, M., Bazterrica, C., Luppi, T. A. and Iribarne, O. O. (2009). An invasive intertidal reef-forming polychaete affect habitat use and feeding behavior of migratory and locals birds in a SW Atlantic coastal lagoon. Journal of Experimental Marine Biology and Ecology 375, 7693. doi:10.1016/j.jembe.2009.05.008.CrossRefGoogle 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. doi:10.1890/06-1036.1.CrossRefGoogle ScholarPubMed
Curtis, L. A. (1997). Ilyanassa obsoleta (Gastropoda) as a host for trematodes in Delaware estuaries. Journal of Parasitology 83, 793803. doi:10.2307/3284270.CrossRefGoogle ScholarPubMed
Curtis, L. A. and Hubbard, K. M. (1990). Trematode infections in a gastropod host misrepresented by observing shed cercarie. Journal of Experimental Marine Biology and Ecology 143, 131137. doi:10.1016/0022-0981(90)90115-S.CrossRefGoogle Scholar
Curtis, L. A. and Hurd, L. E. (1983). Age, sex, and parasites: spatial heterogeneity in a sandflat population of Ilyanassa obsoleta. Ecology 64, 819828. doi:10.2307/1937205.CrossRefGoogle Scholar
De Francesco, C. G. and Isla, F. I. (2003). Distribution and abundance of hydrobiid snails in mixed estuary and coastal lagoon, Argentina. Estuaries 26, 790797. doi:10.1007/BF02711989.CrossRefGoogle Scholar
Esch, G. W. and Fernández, J. (1994). Snail trematode interactions and parasite community dynamics in aquatic systems: a review. The American Midland Naturalist 131, 209237. doi:10.2307/2426248.CrossRefGoogle Scholar
Etchegoin, J. A. (1997). Sistemas parasitarios presentes en la albufera Mar Chiquita. Tesis Doctoral. Facultad de Ciencias Exactas y Naturales. Universidad Nacional de Mar del Plata, Argentina.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. doi:10.2307/3284251.CrossRefGoogle Scholar
Etchegoin, J. A. and Martorelli, S. R. (1998). Nuevos estadios larvales de digeneos parásitos de Heleobia conexa (Mollusca: Hydrobiidae) en Mar Chiquita (Buenos Aires, Argentina). Neotrópica 44, 4150.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. doi:10.1017/S0031182008005027.CrossRefGoogle ScholarPubMed
Fasano, J. L., Hernández, 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 [Spec Publ], 285292.Google Scholar
Ferrero, L. (2001). La avifauna de Mar Chiquita. Sintesis de la tesis Doctoral de M. M. Martínez. In Reserva de Biósfera Mar Chiquita: Características Físicas, Biológicas y Ecológicas (ed. Iribarne, O. O.), pp. 227250. Editorial Martín, Mar del Plata, Argentina.Google Scholar
Jokela, J. and Lively, C. M. (1995). Spatial variation in infection by digenetic trematodes in a population of freshwater snails (Potamopyrgus antipodarum). Oecologia 103, 509517. doi:10.1007/BF00328690.CrossRefGoogle Scholar
Kelly, D. W., Paterson, R. A., Townsend, C. R., Poulin, R. and Tompkins, D. M. (2009). Parasite spillback: a neglected concept in invasion ecology?. Ecology 90, 20472056. doi:10.1890/081085.1.CrossRefGoogle ScholarPubMed
Kube, J., Kube, S. and Dierschke, V. (2002). Spatial and temporal variation in the trematode component community of the mudsnail Hydrobia ventrosa in relation to the occurrence of waterfowl as definitive hosts. Journal of Parasitology 88, 10751086.CrossRefGoogle Scholar
Kuris, A. M. (1991). Guild structure of larval trematodes in molluscan hosts: prevalence, dominance and significance of competition. In Parasite Communities: Patterns and Processes (ed. Esch, G. W., Bush, A. and Aho, J.), pp. 69100. Chapman and Hall, London, UK.Google Scholar
Lafferty, K. D., Sammond, D. T. and Kuris, A. M. (1994). Analysis of larval trematode communities. Ecology 75, 22752285. doi:10.2307/1940883.CrossRefGoogle Scholar
Ludwig, J. A. and Reynolds, J. F. (1988). Statistical Ecology. John Wiley and Sons, Inc. New York. USA.Google Scholar
Luppi, T. A. and Bas, C. C. (2002). The rol of invasive polychaete Ficopomatus enigmatus Fauvel 1923 (Polychaeta: Serpulidae) reefs in the recruitment of Cyrtograpsus angulatus Dana 1851 (Brachyura: Grapsidae) in the Mar Chiquita coastal lagoon, Argentina. Ciencias Marinas 28, 319330.CrossRefGoogle Scholar
Magurran, A. E. (1988). Ecological Diversity and its Measurement. 1st Edn. Princeton University Press, Princeton, NJ, USA.CrossRefGoogle Scholar
Marcogliese, D. J. (2008). The impact of climate change on the parasites and infectious diseases of aquatic animals. Revue scientifique et technique Office international des eÏpizooties 27, 467484.CrossRefGoogle ScholarPubMed
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 Ibérica de Parasitología 46, 373378.Google Scholar
Martorelli, S. R. (1988). El ciclo biológico de Levinseniella cruzi Travassos, 1920 (Digenea, Microphallidae) parásita de los ciegos cólicos de Rollandia rolland chilensis (Aves, Podicipedidae) e Himantopus melanurus (Aves, Recurvirostridae). Iheringia 68, 4962.Google Scholar
Martorelli, S. R. (1989). Estudios parasitológicos en la albufera Mar Chiquita, provincia de Buenos Aires, República Argentina. II. Cercarias (Digenea) parásitas de Heleobia conexa (Mollusca: Hydrobiidae), pertenecientes a las familias Schistosomatidae, Haploporidae y Homalometridae. Neotrópica 35, 8190.Google Scholar
Martorelli, S. R. (1990). Estudios parasitológicos en la albufera Mar Chiquita, provincia de Buenos Aires, República Argentina. III: Sobre dos cercarias parásitas de Heleobia conexa (Mollusca: Hydrobiidae) pertenecientes a la superfamilia Echinostomatoidea. Neotrópica 36, 5563.Google Scholar
Martorelli, S. R. (1991). El ciclo biológico de Microphallus simillimus (Travassos, 1920), comb. n. (Digenea: Microphallidae), parásito de Heleobia conexa (Mollusca: Hydrobiidae) y de Himantopus melanurus (Aves: Recurvirostridae) en Argentina. Iheringia 71, 9198.Google Scholar
Martorelli, S. R. and Etchegoin, J. A. (1996). Cercarias de la superfamilia Opistorchioidea en Heleobia conexa (Mollusca: Hydrobiidae) de la albufera de Mar Chiquita. Neotrópica 42, 6167.Google Scholar
Merlo, M. J. (2009). Los sistemas molusco-trematode como indicadores ambientales en la laguna Mar Chiquita, provincia de Buenos Aires. Tesis de Licenciatura. Facultad de Ciencias Exactas y Naturales, Universidad Nacional de Mar del Plata, Argentina.Google Scholar
Merlo, M. J. and Etchegoin, J. A. (2011). Testing temporal stability of the larval digenean community in Heleobia conexa (Mollusca: Cochliopidae) and its possible use as an indicator of environmental fluctuations. Parasitology 138, 249256. doi:10.1017/S0031182010001150.CrossRefGoogle ScholarPubMed
Merlo, M. J., Parietti, M. and Etchegoin, J. A. (2010). Evaluation of species richness estimators in studies of diversity involving two larval digenean communities parasitizing snail hosts. Parasitology Research 107, 10931102. doi: 10.1007/s00436-010-1977-9.CrossRefGoogle ScholarPubMed
Obenat, S. and Pezzani, S. (1994). Life cycle and population structure of the polychaete Ficopomatus enigmaticus (Serpulidae) in Mar Chiquita coastal lagoon, Argentina. Estuaries 17, 263270. doi:10.2307/1352574.CrossRefGoogle Scholar
Obenat, S., Spivak, E., and Garrido, L. (2006). Life history and reproductive biology of the invasive amphipod Melita palmata (Amphipoda: Melitidae) in the Mar Chiquita coastal lagoon, Argentina. Journal of the Marine Biological Association of the United Kingdom 86, 13811387. doi:10.1017/S002531540601441X.CrossRefGoogle Scholar
Orensanz, J. M. and Estivariz, M. C. (1972). Los anélidos poliquetos de aguas salobres de la Provincia de Buenos Aires. Revista del Museo de La Plata 11, 95112.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. doi:10.1017/S0031182005008693.CrossRefGoogle ScholarPubMed
Poulin, R. (2007). The structure of parasite communities in fish hosts: ecology meets geography and climate. Parassitologia 49, 169172.Google ScholarPubMed
Poulin, R., Paterson, R. A., Townsend, C. R., Tompkins, D. M. and Kelly, D. W. (2011). Biological invasions and the dynamics of endemic diseases in freshwater ecosystems. Freshwater Biology 56, 676688. doi:10.1111/j.1365-2427.2010.02425.x.CrossRefGoogle Scholar
Reta, R., Martos, P., Perillo, G. M. E., Piccolo, M. C. and Ferrante, A. (2001). Características hidrográficas del estuario de la laguna Mar Chiquita. In Reserva de Biósfera Mar Chiquita: Características Físicas, Biológicas y Ecológicas (ed. Iribarne, O. O.), pp. 3152. Editorial Martín, Mar del Plata, Argentina.Google Scholar
Schwindt, E., Bortolus, A. and Iribarne, O. O. (2001). Invasion of a reef-builder polychaete: direct and indirect impacts on the native benthic community structure. Biological Invasions 3, 137149. doi:10.1023/A:1014571916818.CrossRefGoogle Scholar
Schwindt, E., Iribarne, O. and Isla, I. (2004a). Physical effects of an invading reefbuilding polychaete on an Argentinean estuarine environment. Estuarine, Coastal and Shelf Science 59, 109120. doi:10.1016/j.ecss.2003.06.004.CrossRefGoogle Scholar
Schwindt, E., De Francesco, C. G. and Iribarne, O. O. (2004b). Individual and reef growth of the introduced reef-building polychaete Ficopomatus enigmaticus in a south-western Atlantic coastal lagoon. Journal of the Marine Biological Associattion of the United Kingdom 84, 987993. doi:10.1017/S0025315404010288h.CrossRefGoogle 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. doi:10.1645/GE-118R.CrossRefGoogle Scholar
Sousa, W. P. (1991). Spatial scale and the processes structuring a guild of larval trematode parasites. In Parasite Communities: Patterns and Processes (ed. Esch, G. W., Bush, A. and Aho, J.), pp. 4167. Chapman and Hall, London, UK.Google Scholar
Zar, J. H. (2009). Biostatistical Analysis. 5th Edn. Pearson Education, Inc. New Jersey, USA.Google Scholar