Hostname: page-component-78c5997874-v9fdk Total loading time: 0 Render date: 2024-11-03T02:22:28.149Z Has data issue: false hasContentIssue false
  • English
  • Français

Effects of local hydrodynamic regime on the individual's size in intertidal Sabellaria (Annelida: Polychaeta: Sabellariidae) and associated fauna at Cabo Branco beach, north-east Brazil

Published online by Cambridge University Press:  24 October 2011

Cecília Lomônaco ,
André S. Santos  and
Martin L. Christoffersen
Cecília Lomônaco
Affiliation:
Laboratório de Ecologia Evolutiva, Instituto de Biologia, Universidade Federal de Uberlândia, 38.400-902, Uberlândia, Minas Gerais, Brazil
André S. Santos
Affiliation:
Departamento de Sistemática e Ecologia, Centro de Ciências Exatas e da Natureza, Universidade Federal da Paraíba Campus I, 58.059-900, João Pessoa, Paraíba, Brazil
Martin L. Christoffersen*
Affiliation:
Departamento de Sistemática e Ecologia, Centro de Ciências Exatas e da Natureza, Universidade Federal da Paraíba Campus I, 58.059-900, João Pessoa, Paraíba, Brazil
*
Correspondence should be addressed to: M.L. Christoffersen, Departamento de Sistemática e Ecologia, Centro de Ciências Exatas e da Natureza, Universidade Federal da Paraíba Campus I, 58.059-900, João Pessoa, Paraíba, Brazil email: [email protected]
Get access

Abstract

We aimed to verify the effects of local environmental hydrodynamics on the individual size of two sand-reef sabellariids (Sabellaria wilsoni and S. nanella) on a tropical intertidal beach in north-east Brazil. We also tested the hypothesis that the richness and abundance of their reef-building associated fauna would be influenced by environmental conditions related to the wind and wave action intensity. Individuals from three distinct intertidal levels at Cabo Branco beach (7o8′46″S 34°47′55″W), João Pessoa, Paraíba, Brazil, were sampled, identified, sexed, measured and the fauna associated with the reef samples was identified and quantified. Our statistical tests indicated that reef builders have distinct organization patterns which are related to environmental conditions. The aggregates exposed to the strongest wave and wind conditions presented reduced density and sabellariids of smaller sizes in comparison with the other aggregates. The associated fauna abundance and composition was also influenced by the local hydrodynamic regime.

Keywords

community structureenvironmental hydrodynamicstropical marine faunaSabellariidaeSabellaria
Type
Research Article
Information
Marine Biodiversity Records , Volume 4 , December 2011 , e76
Copyright
Copyright © Marine Biological Association of the United Kingdom 2011

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

Achary, G.P.K. (1974) Polychaetes of the family Sabellariidae with special reference to their intertidal habitat. Proceedings of the Indian National Science Academy 38, 442–455.Google Scholar
Agrawal, A.A. (2001) Phenotypic plasticity in the interactions and evolution of species. Science 294, 321–326.CrossRefGoogle ScholarPubMed
Borgia, G. (1979) Sexual selection and the evolution of mating systems. In Blum, S.M. and Blum, N.A. (eds) Sexual selection and reproductive competition in insects. New York: Academic Press, pp. 19–80.Google Scholar
Cognie, B., Haure, J. and Barillé, L. (2006) Spatial distribution in a temperate coastal ecosystem of the wild stock of the farmed oyster Crassostrea gigas (Thunberg). Aquaculture 259, 249–259.CrossRefGoogle Scholar
Cooper, K., Boyd, S., Aldridge, J. and Rees, H. (2007) Cumulative impacts of aggregate extraction on seabed macro-invertebrate communities in an area off the east coast of the United Kingdom. Journal of Sea Research 57, 288–302.CrossRefGoogle Scholar
Davies, A.J., Last, K.S., Attard, K. and Hendrix, V.J. (2009) Maintaining turbidity and current flow in laboratory aquarium studies: a case study using Sabellaria spinulosa. Journal of Experimental Marine Biology and Ecology 370, 35–40.CrossRefGoogle Scholar
De Jong, G. (1995) Phenotypic plasticity as a product of selection in a variable environment. American Naturalist 145, 493–512.CrossRefGoogle Scholar
Dubois, S., Commito, J., Olivier, F. and Retiere, C. (2006) Effects of epibionts on Sabellaria alveolata (L.) biogenic reef sand and their associated fauna in the Bay of Mont Saint-Michel. Estuarine, Coastal and Shelf Science 68, 635–646.CrossRefGoogle Scholar
Fausto-Filho, J. and Furtado, E. (1970) Nota preliminar sobre a fauna das colônias de Sabellariidae do litoral do Estado do Ceará (Annelida, Sedentaria). Revista Brasileira de Biologia 30, 285–289.Google Scholar
Giangrande, A. (1997) Polychaete reproductive patterns, life cycle and life histories: an overview. Oceanography and Marine Biology: an Annual Review 35, 323–386.Google Scholar
Gorur, G., Lomônaco, C. and Mackenzie, A. (2005) Phenotypic plasticity in host-plant specialisation in Aphis fabae. Ecological Entomology 30, 657–664.CrossRefGoogle Scholar
Holt, T.J., Rees, E.I., Hawkins, S.J. and Seed, R. (1998) Biogenic reefs. An overview of dynamic and sensitivity characteristics for conservation management of marine SACs. Volume 4. Liverpool: Scottish Association for Marine Science, 170 pp.Google Scholar
Honeck, A. (1993) Intraspecific variation in body size and fecundity in insects: a general relationship. Oikos 66, 483–492.CrossRefGoogle Scholar
Hutchenson, K. (1970) A test for comparing diversities based on the Shannon formula. Journal of Theoretical Biology 29, 151–154.CrossRefGoogle Scholar
Hutchings, P.A. (2000) Family Sabellariidae. In Beesley, P.L., Ross, G.J.B. and Glasby, C.J. (eds) Polychaetes & allies: the southern synthesis. Fauna of Australia. Polychaeta, Mystozomida, Pogonophora, Equiura, Sipuncula, Volume 4. Melbourne: CSIRO Publishing, pp. 115–218.Google Scholar
Jones, L.A., Hiscock, K. and Connor, D.W. (2000) Marine habitat reviews. A summary of ecological requirements and sensitivity characteristics for conservation and management of marine SACs. Peterborough: Joint Nature Conservation Committee, 178 pp.Google Scholar
Kirtley, D.W. (1994) A review and taxonomic revision of the family Sabellariidae Johnston, 1865 (Annelida; Polychaeta). Vero Beach, FL: Sabecon Press Science Series.Google Scholar
Lana, P.C. and Bremec, C.S. (1994) Sabellariidae (Annelida, Polychaeta) from South America. In Dauvin, J.C., Laubier, L. and Reish, D.J. (eds) Actes de la 4ème Conference Internacionale des Polychètes. Mémoires du Muséum National d'Historire Naturelle de Paris 162, 211–222.Google Scholar
Lana, P.C. and Gruet, Y. (1989) Sabellaria wilsoni sp. n. (Polychaeta, Sabellariidae) from the southeast coast of Brazil. Zoologica Scripta 18, 239–244.CrossRefGoogle Scholar
La Porta, B., La Valle, P. and Chimenz, G. (2006) Sabellaria alveolata (Linnaeus, 1776): la selezione dei granuli di sedimento per la costruzione dei tubi. Biologia Marina Mediterranea 13, 593–596.Google Scholar
La Porta, B., Targusi, M., Lattanzi, L., La Valle, P., Paganelli, D. and Nicoletti, L. (2009) Relict sand dredging for beach nourishment in the central Tyrrhenian Sea (Italy): effects on benthic assemblages. Marine Ecology 30, 97–104.CrossRefGoogle Scholar
Lerner, I.M. (1954) Genetic homeostasis. London: Oliver and Boyd.Google Scholar
Lima, P.J. and Heckendorff, W.D. (1985) Climatologia. Governo do Estado da Paraíba. Atlas do Estado da Paraíba. João Pessoa: Grafset.Google Scholar
Magurran, A.E. (1989) Ecological diversity and its measurement. Princeton, NJ: Princeton University Press.Google Scholar
Manly, B.F.J. (1994) Multivariate statistical methods. A primer. London: Chapman and Hall.Google Scholar
Nimer, E. (1977) Clima. Fundação Instituto Brasileiro de Geografia e Estatística. Geografia do Brasil: Região Nordeste, Volume 2. Rio de Janeiro: Instituto Brasileiro de Geografia e Estatística, 454 pp.Google Scholar
Occhioni, G., Brasil, A.C.S. and Araújo, A.F.B. (2009) Morphometric study of Phragmatopoma caudate (Polychaeta: Sabellida: Sabellaridae). Zoologia 26, 739–746.CrossRefGoogle Scholar
Porras, R., Bataller, J.V., Murgui, E. and Torregrosa, M.T. (1996) Trophic structure and community composition of polychaetes inhabiting some Sabellaria alveolata (L.) reefs along the Valencia Gulf Coast, Western Mediterranean. Marine Ecology 17, 583–602.CrossRefGoogle Scholar
Posey, M.H., Pregnal, A.M. and Graham, R.A. (1984) A brief description of a subtidal sabellariid (Polychaeta) reef on the southern Oregon coast. Pacific Science 38, 28–33.Google Scholar
Rodrigues, F.M.A., Lomônaco, C. and Christoffersen, M.L. (2009) Habitat partition, and variations of size and symmetry of three sympatric species of Alpheus (Decapoda: Caridea) along an intertidal gradient in the southwestern Atlantic. Journal of Crustacean Biology 29, 333–441.Google Scholar
Rossiter, M.C. (1996) Incidence and consequences of inherited environmental effects. Annual Review of Ecology, Evolution, and Systematics 27, 451–476.CrossRefGoogle Scholar
Rullier, F. and Amoureux, L. (1979) Campagne de la Calypso au large des côtes atlantiques de ĺAmerique du Sud (1961–1962). I. 33. Annélides polychétes. Annales de l'Institut Océanographique de Monaco Supplement 55, 145–206.Google Scholar
Santos, P.J.P.D. (1991) Morphodynamical influence of a temporary freshwater stream on the population dynamics of Scolelepis gaucha (Polychaeta: Spionidae) on a sandy beach in southern Brazil. Bulletin of Marine Science 48, 657–664.Google Scholar
Scheiner, S.M. (1993) Genetics and evolution of phenotypic plasticity. Annual Review of Ecology, Evolution, and Systematics 24, 35–68.CrossRefGoogle Scholar
Schmidt-Nielsen, K. (1984) Scaling: why is animal size so important? Cambridge: Cambridge University Press.CrossRefGoogle Scholar
Seiderer, L.J. and Newell, R.C. (1999) Analysis of relationship between sediment composition and benthic community structure in coastal deposits: implications for marine aggregate dredging. Journal of Marine Science 56, 757–765.Google Scholar
Stearns, S.C. (1992) The evolution of life stories. Oxford: Oxford University Press.Google Scholar
Suguio, K. and Nogueira, A.C.R. (1999) Revisão crítica dos conhecimentos geológicos sobre a Formação (ou grupo) Barreiras do Neógeno e o seu possível significado como testemunho de alguns eventos geológicos mundiais. Geociências 18, 461–479.Google Scholar
Vaz, L.A.L., Tavares, M. and Lomônaco, C. (2004) Diversidade e tamanho de himenópteros parasitóides de Brevicoryne brassicae L. e Aphis nerii Boyer de Foscolombe (Hemiptera: Aphididae). Neotropical Entomology 33, 225–230.CrossRefGoogle Scholar
Vorberg, R. (1995) On the decrease of sabellarian reefs along the German North Sea. Publicacion Service de Géologie Luxembourg 29, 87–93.Google Scholar
Young, P.S. (1986) Análise qualitativa e quantitativa da fauna associada a corais hermatípicos (Coelenterata, Scleractinia) nos recifes de João Pessoa, PB. Revista Brasileira de Biologia 46, 99–126.Google Scholar
Zar, J.H. (1984) Biostatistical analysis. Englewood Cliffs, NJ: Prentice-Hall.Google Scholar