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Population dynamics of the harvested clam Anomalocardia brasiliana (Bivalvia: Veneridae) in Cidade Beach, south-east Brazil

Published online by Cambridge University Press:  23 March 2015

Guilherme Nascimento Corte Open the ORCID record for Guilherme Nascimento Corte [Opens in a new window] ,
Leonardo Querobim Yokoyama ,
Ross A. Coleman  and
A. Cecília Z. Amaral
Guilherme Nascimento Corte*
Affiliation:
Programa de Pós-Graduação em Ecologia, Departamento de Biologia Animal, Instituto de Biologia, Universidade Estadual de Campinas, Campinas, São Paulo, Brasil
Leonardo Querobim Yokoyama
Affiliation:
Departamento de Biologia Animal, Instituto de Biologia, Universidade Estadual de Campinas, Campinas, SP, Brasil
Ross A. Coleman
Affiliation:
School of Biological Sciences, The University of Sydney, Sydney, New South Wales, Australia
A. Cecília Z. Amaral
Affiliation:
Departamento de Biologia Animal, Instituto de Biologia, Universidade Estadual de Campinas, Campinas, São Paulo, Brasil
*
Correspondence should be addressed to: G. N. Corte, Programa de Pós-Graduação em Ecologia, Departamento de Biologia Animal, Instituto de Biologia, Universidade Estadual de Campinas, Campinas, São Paulo, Brasil email: [email protected]
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Abstract

Knowledge of the population dynamics and productivity of exploited species is essential to achieve the sustainable development of fisheries, and to ensure sustainable, long-term use of these resources. The venerid clam Anomalocardia brasiliana is harvested as a fishery resource from the French West Indies to Brazil. Yet, the exploitation of this species is not backed by management or regulations based on scientific knowledge. This can result in reduced (or even depleted) A. brasiliana density and biomass. Here, we examined the population dynamics of A. brasiliana over the course of 1 year at Cidade Beach, a sheltered sandy beach located in south-eastern Brazil. Sampling was done monthly from March 2007 to February 2008. The sampled population was predominantly juvenile. Growth and recruitment were continuous, indicating no major fluctuation in limiting factors, such as temperature, salinity and food. Nevertheless, the abundance and the turnover rate (P/B ratio) of A. brasiliana at Cidade were much smaller than the values observed in other areas of occurrence. The mortality was more intense in young individuals, and the peak of individual production occurred in individuals with a 25 mm shell length, suggesting that individuals smaller than this size should not be exploited.

Keywords

fisheriesgrowthproductionmortalitybivalve
Type
Research Article
Information
Journal of the Marine Biological Association of the United Kingdom , Volume 95 , Issue 6 , September 2015 , pp. 1183 - 1191
Copyright
Copyright © Marine Biological Association of the United Kingdom 2015 

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References

REFERENCES

Amaral, A.C.Z. and Denadai, M.R. (2011) Caracterização das praias arenosas. In: Amaral, A.C.Z. and Nallin, S.A.H. (eds) Biodiversidade e Ecossistemas Bentônicos Marinhos do Litoral Norte de São Paulo, Sudeste do Brasil. 1st ed.Campinas (SP): UNICAMP/IB, pp. 354–369.Google Scholar
Anderson, S.C., Flemming, J.M., Watson, R. and Lotze, H.K. (2011) Rapid global expansion of invertebrate fisheries: trends, drivers, and ecosystem effects. PLoS ONE 6, e14735.CrossRefGoogle ScholarPubMed
Arruda-Soares, H., Schaeffrer-Novell, Y. and Mandelli, J. Jr (1982) Berbigão Anomalocardia brasiliana (Gmelin, 1791), bivalve comestível da região da Ilha do Cardoso, Estado de São Paulo, Brasil: Aspectos biológicos de interesse para a pesca comercial. Boletim do Instituto de Pesca 9, 21–38.Google Scholar
Barreira, C.A.R. and Araujo, M.L.R. (2005) Ciclo reprodutivo de Anomalocardia brasiliana (Gmelin, 1791) (Mollusca, Bivalvia, Veneridae) na praia do Canto da Barra, Fortim, Ceará, Brasil. Boletim do Instituto de Pesca 31, 9–20.Google Scholar
Bayne, B.L., Thompson, R.J. and Widdows, J. (1976) Physiology. In Bayne, B.L. (ed) Marine mussels: their ecology and physiology. Cambridge: Cambridge University Press, pp. 121–206.Google Scholar
Benke, A.C. (1993) Concepts and patterns of invertebrate production in running waters. Verhandlungen des Internationalen Verein Limnologie 25, 15–28.Google Scholar
Boehs, G., Absher, T.M. and Cruz-Kaled, A.C. (2008) Ecologia populacional de Anomalocardia brasiliana (Gmelin, 1791) (Bivalvia, Veneridae) na Baía de Paranaguá, Paraná, Brasil. Boletim do Instituto de Pesca 34, 259–270.Google Scholar
Brey, T. (2001) Population dynamics in benthic invertebrates. A virtual handbook. Version 01.2 at: http://www.thomas-brey.de/science/virtualhandbook.Google Scholar
Castilla, J.C. and Defeo, O. (2001) Latin American benthic shellfisheries: emphasis on co-management and experimental practices. Reviews in Fish Biology and Fisheries 11, 1–30.CrossRefGoogle Scholar
Corte, G.N., Yokoyama, L.Q. and Amaral, A.C.Z. (2014) An attempt to extend the Habitat Harshness Hypothesis to tidal flats: a case study of Anomalocardia brasiliana (Bivalvia: Veneridae) reproductive biology. Estuarine Coastal and Shelf Science 150, 136–141.CrossRefGoogle Scholar
Corte, G.N. (2015) Reproductive cycle and parasitism in the clam Anomalocardia brasiliana (Bivalvia: Veneridae). Invertebrate Reproduction & Development. http://dx.doi.org/10.1080/07924259.2015.1007215CrossRefGoogle Scholar
Crisp, D.J. (1984) Energy flow measurements. In Holme, N.A. and McIntyre, A.D. (eds) Methods for the study of marine benthos, IBP Handbook, Volume 16. Oxford: Blackwell Scientific Publications, pp. 284–372.Google Scholar
Defeo, O. (2003) Marine invertebrate fisheries in sandy beaches: an overview. Journal of Coastal Research 35, 56–65.Google Scholar
Defeo, O., Arreguín-Sánchez, F. and Sánchez, J. (1992) Growth study of the yellow clam Mesodesma mactroides: a comparative analysis of three length-based methods. Scientia Marina 56, 53–59.Google Scholar
Defeo, O., Gomez, J. and Lercari, D. (2001) Testing the swash exclusion hypothesis in sandy beach populations: the mole crab Emerita brasiliensis in Uruguay. Marine Ecology Progress Series 212, 159–170.CrossRefGoogle Scholar
Defeo, O., Lercari, D. and Gomez, J. (2003) The role of morphodynamics in structuring sandy beach populations and communities: what should be expected? Journal of Coastal Research 35, 352–362.Google Scholar
Defeo, O. and Rueda, M. (2002) Spatial structure, sampling design and abundance estimates in sandy beach macroinfauna: some warnings and new perspectives. Marine Biology 140, 1215–1225.Google Scholar
Dolbeth, M., Cusson, M., Sousa, R. and Pardal, M.A. (2012) Secondary production as a tool for better understanding of aquatic ecosystems. Canadian Journal of Fisheries and Aquatic Sciences 69, 1230–1253.CrossRefGoogle Scholar
Folk, R.L. and Ward, W.C. (1957) Brazos river bar: a study in the significance of grain size parameters. Journal of Sedimentary Petrology 27, 3–26.CrossRefGoogle Scholar
Fröcklin, S., de la Torre-Castro, M., Hakansson, E., Carlsson, A., Magnusson, M. and Jiddawi, N.S. (2014) Towards improved management of tropical invertebrate fisheries: including time series and gender. PLoS ONE 9, e91161. doi: 10.1371/journal.pone.0091161.CrossRefGoogle ScholarPubMed
García-Berthou, E., Carmona-Catot, G., Merciai, R. and Ogle, D.H. (2012) A technical note on seasonal growth models. Reviews in Fish Biology and Fisheries 22, 635–640.CrossRefGoogle Scholar
Gayanilo, F.C., Sparre, P. and Pauly, D. (2005) FAO-ICLARM Stock Assessment Tools II (FiSAT II). Revised version. User's guide. FAO Computerized Information Series (Fisheries). No. 8, Revised version. Rome: FAO. 168 pp.Google Scholar
Gómez, J. and Defeo, O. (1999) Life history of the sandhopper Pseudorchestoidea brasiliensis (Amphipoda) in sandy beaches with contrasting morphodynamics. Marine Ecology Progress Series 182, 209–220.CrossRefGoogle Scholar
Hobday, A.L., Tegner, M.J. and Haaker, P.L. (2001) Over-exploitation of a broadcast spawning marine invertebrate: decline of the white abalone. Reviews in Fish Biology and Fisheries 10, 493–514.CrossRefGoogle Scholar
Lomovasky, B.J., Brey, T. and Morriconi, E. (2005) Population dynamics of the venerid bivalve Tawera gayi (Hupé, 1854) in the Ushuaia Bay, Beagle Channel. Journal of Applied Ichthyology 21, 64–69.CrossRefGoogle Scholar
McArdle, S.B. and McLachlan, A. (1991) Dynamics of the swash zone and effluent line on sandy beaches. Marine Ecology Progress Series 76, 91–99.CrossRefGoogle Scholar
McArdle, S.B. and McLachlan, A. (1992) Sand beach ecology: swash features relevant to the macrofauna. Journal of Coastal Research 8, 398–407.Google Scholar
Mattos, G. and Cardoso, R.S. (2012) Population dynamics of two suspension-feeding bivalves on a sheltered beach in southeastern Brazil. Helgoland Marine Research 66, 393–400. doi: 10.1007/s10152–011-0280-1.CrossRefGoogle Scholar
McLachlan, A. and Brown, A.C. (2006) The ecology of sandy shores. 2nd edn.Burlington, MA: Academic Press.Google Scholar
McLachlan, A. and Dorvlo, A. (2005) Global patterns in sandy beach macrobenthic communities. Journal of Coastal Research 21, 674–687.CrossRefGoogle Scholar
Mendonça, V.D., Raffaelli, D.J. and Boyle, P.R. (2007) Interactions between shorebirds and benthic invertebrates at Culbin Sands lagoon, NE Scotland: effects of avian predation on their prey community density and structure. Scientia Marina 71, 579–591.CrossRefGoogle Scholar
Metaxatos, A. (2004) Population dynamics of the venerid bivalve Callista chione L. in a coastal area of the eastern Mediterranean. Journal of Sea Research 52, 293–305.CrossRefGoogle Scholar
Monti, D., Frenkiel, L. and Moueza, M. (1991) Demography and growth of Anomalocardia brasiliana (Gmelin) (Bivalvia: Veneridae) in a mangrove, in Guadeloupe (French West Indies). Journal of Molluscan Studies 57, 249–257.CrossRefGoogle Scholar
Mouëza, M., Gros, O. and Frenkiel, L. (1999) Embryonic, larval and postlarval development of the tropical clam, Anomalocardia brasiliana, Bivalvia: Veneridae). Journal of Molluscan Studies 64, 73–88.CrossRefGoogle Scholar
Moura, P., Gaspar, M.B. and Monteiro, C.C. (2009) Age determination and growth rate of a Callista chione population from the southwestern coast of Portugal. Aquatic Biology 5, 97–106.CrossRefGoogle Scholar
Olafson, E.B. (1989) Contrasting influences of suspension-feeding and deposit-feeding populations of Macoma balthica on infaunal recruitment. Marine Ecology Progress Series 55, 171–179.CrossRefGoogle Scholar
Ortega Cisneros, K., Smit, A.J., Laudien, J. and Schoeman, D.S. (2011) Complex, dynamic combination of physical, chemical and nutritional variables controls spatio-temporal variation of sandy beach community structure. PLoS ONE 6, e23724. doi: 10.1371/journal.pone.0023724.CrossRefGoogle Scholar
Pauly, D. (1983) Length-converted catch curves: a powerful tool for fisheries research in the tropics (part I). Fishbyte 1, 9–13.Google Scholar
Pauly, D. and Munro, J.L. (1984) Once more on the comparison of growth in fish and invertebrates. Fishbyte 2, 21.Google Scholar
Peterson, C.H. (1982) The importance of predation and intra- and interspecific competition in the population biology of two infaunal suspension-feeding bivalves, Protothaca staminea and Chione undatella. Ecological Monographs 52, 437–475.CrossRefGoogle Scholar
Peterson, C.H. and Black, R. (1987) Resource depletion by active suspension feeders on tidal flats: influence of local density and tidal elevation. Limnology and Oceanography 32, 143–166.CrossRefGoogle Scholar
Petracco, M., Cardoso, R.S. and Turra, A. (2013) Patterns of sandy-beach macrofauna production. Journal of the Marine Biological Association of United Kingdom 93, 1717–1725.CrossRefGoogle Scholar
Petracco, M., Veloso, V.G. and Cardoso, R.S. (2003) Population dynamics and secondary production of Emerita brasiliensis (Crustacea: Hippidae) at Prainha. Marine Ecology 24, 231–245.CrossRefGoogle Scholar
Pezzuto, P.R., Schio, C. and Almeida, T.C.M. (2010) Efficiency and selectivity of the Anomalocardia brasiliana (Mollusca: Veneridae) hand dredge used in southern Brazil. Journal of the Marine Biological Association of United Kingdom 90, 1455–1464.CrossRefGoogle Scholar
Rodrigues, A.M.L., Borges-Azevedo, C.M., Costa, R.S. and Henry-Silva, G.G. (2013) Population structure of the bivalve Anomalocardia brasiliana (Gmelin, 1791) in the semi-arid estuarine region of northeastern Brazil. Brazilian Journal of Biology 73, 819–833.CrossRefGoogle ScholarPubMed
Schoeman, D.S. and Richardson, A.J. (2002) Investigating biotic and abiotic factors affecting the recruitment of an intertidal clam on an exposed sandy beach using a generalized additive model. Journal of Experimental Marine Biology and Ecology 276, 67–81.CrossRefGoogle Scholar
Seitz, R.D., Lipcius, R.N., Hines, A.H. and Eggleston, D.B. (2001) Density-dependent predation, habitat variation, and the persistence of marine bivalve prey. Ecology 82, 2435–2451.CrossRefGoogle Scholar
Silva-Cavalcanti, J. and Costa, M. (2009) Fisheries in protected and non-protected areas: is it different? The case of Anomalocardia brasiliana at tropical estuaries of northeast Brazil. Journal of Coastal Research 56, 1454–1458.Google Scholar
Silva-Cavalcanti, J. and Costa, M. (2011) Fisheries of Anomalocardia brasiliana tropical estuaries. Pan-American Journal of Aquatic Sciences 6, 86–89.Google Scholar
Somers, I.F. (1988) On a seasonally oscillating growth function. Fishbyte 6, 8–11.Google Scholar
Sparre, P., Ursin, E. and Venema, S. (1989) Introduction to tropical fish stock assessment. Part I. Fao Fisheries Technical Paper 306/1 Rev. 2. Rome: FAO, 407 pp.Google Scholar
Turra, A., Petracco, M., Amaral, A.C.Z. and Denadai, M.R. (2014a) Population biology and secondary production of the harvested clam Tivela mactroides (Born, 1778) (Bivalvia, Veneridae) in southeastern Brazil. Marine Ecology doi: 10.1111/maec.12137.Google Scholar
Turra, A., Petracco, M., Amaral, A.C.Z. and Denadai, M.R. (2014b) Temporal variation in life-history traits of the clam Tivela mactroides (Bivalvia: Veneridae): density-dependent processes in sandy beaches. Estuarine Coastal and Shelf Science 150, 157–164.CrossRefGoogle Scholar
Urban, H.J. (2000) Culture potential of the pearl oyster (Pinctada imbricata) from the Caribbean. I. Gametogenic activity, growth, mortality and production of a natural population. Aquaculture 189, 361–373.CrossRefGoogle Scholar
Urban, H.J. and Campos, B. (1994) Population dynamics of the bivalves Gari solida, Semele solida and Protothaca thaca from a small bay in Chile at 36″ S. Marine Ecology Progress Series 115, 93–102.CrossRefGoogle Scholar
Waters, T.F. (1977) Secondary production in inland waters. Advances in Ecological Research 10, 91–164.CrossRefGoogle Scholar
Wilson, W.H. (1990) Competition and predation in marine soft-sediment communities. Annual Review of Ecology and Systematics 21, 221–241.CrossRefGoogle Scholar
Woodin, S.A. (1976) Adult-larval interactions in dense infaunal assemblages: patterns of abundance. Journal of Marine Research 34, 24–41.Google Scholar
Yokoyama, L.Q. and Amaral, A.C.Z. (2011) Allometric growth of a common Nassariidae (Gastropoda) in south-east Brazil. Journal of the Marine Biological Association of the United Kingdom 91, 1095–1105.CrossRefGoogle Scholar