Hostname: page-component-77c89778f8-sh8wx Total loading time: 0 Render date: 2024-07-23T13:02:45.177Z Has data issue: false hasContentIssue false

The brown mussel Perna perna in the native mussel beds of Cerro Verde (Uruguay)

Published online by Cambridge University Press:  16 April 2009

Alvar Carranza*
Affiliation:
Investigación & Desarrollo, Facultad de Ciencias, Iguá 4225, C.P.11.400, Montevideo, Uruguay UNDECIMAR, Facultad de Ciencias, Iguá 4225, C.P.11.400, Montevideo, Uruguay
Ana Inés Borthagaray
Affiliation:
Investigación & Desarrollo, Facultad de Ciencias, Iguá 4225, C.P.11.400, Montevideo, Uruguay Departamento de Ecología and Centro de Estudios Avanzados en Ecología y Biodiversidad (CASEB), Pontificia Universidad Católica de Chile, Casilla 114-D, Santiago, Chile Instituto de Ecología y Biodiversidad (IEB), Casilla 653, Santiago, Chile. (Equal authorship)
*
Correspondence should be addressed to: A. Carranza, Investigación & Desarrollo, Facultad de Ciencias, Iguá 4225, C.P.11.400, Montevideo, Uruguay email: alvardoc@fcien.edu.uy
Get access

Abstract

Uruguayan mussel beds are located along the estuarine gradient caused by the interaction of the Río de la Plata run-off and the Atlantic Ocean, changing in species composition across this gradient. In the oceanic portion of the gradient, the exotic Perna perna showed a sequence of local extinction–colonization episodes since at least the second half of the 20th Century, thus altering the dominance relationships within the mussel beds. Owing to its larger size, this species may have caused profound effects on the spatial structure of the mussel beds and consequently on its associated macrofauna. In this vein, we analysed patterns in zonation, abundance and dominance of mussel species in a mussel bed located in the oceanic portion of the Uruguayan coast in relation to tidal and exposure level. We also evaluated if these factors could affect the dominance patterns between mussel species. The main results showed that the dominance of the native mussel Brachidontes rodriguezii was consistent across all tidal levels in all sites in terms of absolute and relative abundance, with the exception of the shallow subtidal at the intermediate site, where P. perna dominated over this species in terms of relative abundance. This suggests that the effect of an invasive mussel is highly dependent on the receptive assemblage, and that the outcome of interspecific competition can also be modulated by small-scale factors.

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

REFERENCES

Adami, M.L., Tablado, A. and López Gappa, J. (2004) Spatial and temporal variability in intertidal assemblages dominated by the mussel Brachidontes rodriguezii (d'Orbigny, 1846). Hydrobiologia 520, 4959.CrossRefGoogle Scholar
Amaro, J.A. (1965) La familia Mytilidae en el Uruguay. Revista del Instituto de Investigaciones Pesqueras (Uruguay) 1, 323339.Google Scholar
Barattini, L.P., and Uretta, E.H. (1961) La fauna de las costas del este (Invertebrados). Montevideo: Publicaciones de Divulgación Científica, Museo ‘Dámaso Antonio Larrañaga’.Google Scholar
Borthagaray, A.I. and Carranza, A. (2007) Mussels as ecosystem engineers: their contribution to species richness in a rocky littoral community. Acta Oecologica 31, 243250.CrossRefGoogle Scholar
Carlton, J.T. (1985) Transoceanic and interoceanic dispersal of coastal marine organisms: the biology of ballast water. Oceanography and Marine Biology. Annual Review 23, 313374.Google Scholar
Clavijo, C., Scarabino, F., Rojas, A. and Martínez, S. (2005) Lista sistemática de los moluscos marinos y estuarinos del Cuaternario de Uruguay. Comunicaciones de la Sociedad Malacológica del Uruguay 9, 381411.Google Scholar
del Rio, C.J. (2004) Tertiary marine molluscan assemblages of eastern Patagonia (Argentina); a biostratigraphic analysis. Journal of Paleontology 78, 10971122.2.0.CO;2>CrossRefGoogle Scholar
Erlandsson, J. and McQuaid, C.D. (2004) Spatial structure of recruitment in the mussel Perna perna at local scales: effects of adults, algae and recruit size. Marine Ecology Progress Series 267, 173.CrossRefGoogle Scholar
Giménez, L., Borthagaray, A.I., Rodríiguez, M., Brazeiro, A. and Dimitriadis, C. (2005) Scale-dependent patterns of macrofaunal distribution in soft-sediment intertidal habitats along a large-scale estuarine gradient. Helgoland Marine Research 59, 224236.CrossRefGoogle Scholar
Gutiérrez, J.L., Jones, C.G., Strayer, D.L. and Iribarne, O.O. (2003) Molluscs as ecosystem engineers: the role of shell production in aquatic habitats. Oikos 101, 7990.CrossRefGoogle Scholar
Hanekom, N. (2008) Invasion of an indigenous Perna perna mussel bed on the south coast of South Africa by an alien mussel Mytilus galloprovincialis and its effect on the associated fauna. Biological Invasions 10, 233244.CrossRefGoogle Scholar
Henriques, M.B., Marques, H.L. , d. A., Pereira, O.M. and Bastos, G.C.C. (2004) Aspectos da estrutura populacional do mexilhão Perna perna, relacionados à extração em bancos naturais da Baía de Santos, estado de São Paulo, Brasil. Boletim do Instituto de Pesca, São Paulo 30, 117126.Google Scholar
Hernández, G. and Defeo, O. (2005) Relación masa corporal-abundancia en un gremio de mitílidos suspensívoros del sublitoral rocoso de dos islas de Uruguay. Interciencia 30, 711716.Google Scholar
Ihering, H. von, (1900) On the South American species of Mytilidae. Proceedings of the Malacological Society of London 4, 8498.Google Scholar
IUCN Uruguayan Committee (2002) Áreas marinas protegidas: un enfoque bioregional en el contexto de Manejo Costero Integrado. Montevideo, Uruguay: Facultad de Ciencias.Google Scholar
Klappenbach, M.A. (1965) Lista preliminar de los Mytilidae brasileños con claves para su determinación y notas sobre su distribución. Anais da Academia Brasileira de Ciencias 37, 327352.Google Scholar
Maytía, S. and Scarabino, V. (1979) Las comunidades del litoral rocoso del Uruguay: zonación, distribución local y consideraciones biogeográficas. Memorias del Seminario sobre Ecología Bentónica y Sedimentación de la Plataforma Continental del Atlántico Sur 1, 149160.Google Scholar
McQuaid, C.D. and Branch, G.M. (1985) Trophic structure of rocky intertidal communities: response to wave action and implications for energy flow. Marine Ecology Progress Series 22, 153161.CrossRefGoogle Scholar
McQuaid, C.D. and Lindsay, T.L. (2000) Effect of wave exposure on growth and mortality rates of the mussel Perna perna: bottom up regulation of intertidal populations. Marine Ecology Progress Series 206, 147154.CrossRefGoogle Scholar
Milstein, A., Juanicó, M. and Olazarri, J. (1976) Algunas asociaciones bentónicas frente a las costas de Rocha, Uruguay. Resultados de la campaña del R/V “Hero”, viaje 72–3a. Comunicaciones de la Sociedad Malacológica del Uruguay 4(30), 143164.Google Scholar
Neirotti, E. (1981) Estudio comparativo del supralitoral y mesolitoral rocoso en diferentes localidades del estuario del Río de la Plata. Comunicaciones de la Sociedad Malacológica del Uruguay 5(40), 347370.Google Scholar
Orensanz, J.M.L., Schwindt, E., Pastorino, G., Bortolus, A., Casas, G., Darrigran, G., Elíıas, R., López Gappa, J.J., Obenat, S., Pascual, M., Penchaszadeh, P., Piriz, M.L., Scarabino, F., Spivak, E.D. and Vallarino, E.A. (2002) No longer the pristine confines of the world ocean: a survey of exotic marine species in the south-western Atlantic. Biological Invasions 4, 115143.CrossRefGoogle Scholar
Parmesan, C., Gaines, S., Gonzalez, L., Kaufman, D.M., Kingsolver, J., Townsend Peterson, A. and Sagarin, R. (2005) Empirical perspectives on species borders: from traditional biogeography to global change. Oikos 108, 5875.CrossRefGoogle Scholar
Riestra, G. and Defeo, O. (2000) La comunidad macrobentónica asociada al mejillon Mytilus edulis platensis en costas del departamento de Maldonado: variación espacio-temporal e incidencia del impacto pesquero. In Rey, M. (ed.) Recursos pesqueros no tradicionales: moluscos bentónicos marinos. Montevideo, Uruguay: Proyecto URU/92/003, INAPE-PNUD, pp. 1757.Google Scholar
Rivadeneira, M.M. and Fernández, M. (2005) Shifts in southern endpoints of distribution in rocky intertidal species along the south-eastern Pacific coast. Journal of Biogeography 32, 203209.CrossRefGoogle Scholar
Sagarin, R.D., Barry, J.P., Gilman, S.E. and Baxter, C.H. (1999) Climate-related change in an intertidal community over short and long time scales. Ecological Monographs 69, 465490.CrossRefGoogle Scholar
Sagarin, R.D., Gaines, S.D. and Gaylord, B. (2006) Moving beyond assumptions to understand abundance distributions across the ranges of species. Trends in Ecology and Evolution 21, 524530.CrossRefGoogle ScholarPubMed
Scarabino, F., Zaffaroni, J.C., Clavijo, C., Carranza, A. and Nin, M. (2006a) Bivalvos marinos y estuarinos de la costa uruguaya: faunística, distribución, taxonomía y conservación. In Menafra, R. et al. (eds) Bases para la conservación y el manejo de la costa uruguaya. Montevideo, Uruguay: VIDA SILVESTRE (Sociedad Uruguaya para la Conservación de la Naturaleza), pp. 157169.Google Scholar
Southward, A.J. (1991) Forty years of changes in species composition and population density of barnacles on a rocky shore near Plymouth. Journal of the Marine Biological Association of the United Kingdom 71, 495.CrossRefGoogle Scholar
Steffani, C.N. and Branch, G.M. (2005) Mechanisms and consequences of competition between an alien mussel, Mytilus galloprovincialis, and an indigenous limpet, Scutellastra argenvillei. Journal of Experimental Marine Biology and Ecology 317, 127142.CrossRefGoogle Scholar
Stephenson, T.A. and Stephenson, A. (1949) The universal features of zonation between tide-marks on rocky coasts. Journal of Ecology 37, 289305.CrossRefGoogle Scholar
Wood, A.R., Apte, S., MacAvoy, E.S. and Gardner, J.P.A. (2007) A molecular phylogeny of the marine mussel genus Perna (Bivalvia: Mytilidae) based on nuclear (ITS1 & 2) and mitochondrial (COI) DNA sequences. Molecular Phylogenetics and Evolution 44, 685698.CrossRefGoogle Scholar
Zaffaroni, J.C. (2000) Presencia de Modiolus carvalhoi (Mollusca, Pelecypoda) en aguas uruguayas. Comunicaciones de la Sociedad Malacológica del Uruguay 8, 101103.Google Scholar