Hostname: page-component-78c5997874-ndw9j Total loading time: 0 Render date: 2024-11-05T10:30:48.972Z Has data issue: false hasContentIssue false

Allometry and population structure of Nicolea uspiana (Polychaeta: Terebellidae)

Published online by Cambridge University Press:  12 February 2010

A.R.S. Garraffoni*
Affiliation:
Laboratório de Macrobentos Marinho, Departamento de Biologia Animal, Instituto de Biologia, Universidade Estadual de Campinas, CEP: 13083-970, CP: 6109, Campinas, Brazil
L.Q. Yokoyama
Affiliation:
Pós-Graduação em Zoologia, Departamento de Zoologia, IB, Universidade de São Paulo, São Paulo, Brazil Laboratório de Macrobentos Marinho, Departamento de Biologia Animal, Instituto de Biologia, Universidade Estadual de Campinas, CEP: 13083-970, CP: 6109, Campinas, Brazil
A.C.Z. Amaral*
Affiliation:
Laboratório de Macrobentos Marinho, Departamento de Biologia Animal, Instituto de Biologia, Universidade Estadual de Campinas, CEP: 13083-970, CP: 6109, Campinas, Brazil
*
Correspondence should be addressed to: A.R.S. Garraffoni and A.C.Z. Amaral, Laboratório de Macrobentos Marinho, Departamento de Biologia Animal, Instituto de Biologia, Universidade Estadual de Campinas, CEP: 13083-970, CP: 6109 Campinas, Brazil emails: [email protected]; [email protected]
Correspondence should be addressed to: A.R.S. Garraffoni and A.C.Z. Amaral, Laboratório de Macrobentos Marinho, Departamento de Biologia Animal, Instituto de Biologia, Universidade Estadual de Campinas, CEP: 13083-970, CP: 6109 Campinas, Brazil emails: [email protected]; [email protected]

Abstract

The relative growth and population structure of the terebellid Nicolea uspiana were investigated in the intertidal zone of a rocky shore on the south-east coast of Brazil, from May 2006 to May 2007. Eight hundred and forty-seven individuals of N. uspiana were analysed: 391 males, 163 females, and 293 immatures. Although significant differences in some morphometric parameters were found, there was no sexual dimorphism between males and females. There were differences in total length, width of segment 5, and length of the notopodial region between matures and immatures. The negative allometry of the total length in relation to five other parameters showed that this feature is a good measure for estimating the individual size, which was then used in the analysis of population structure. This population of N. uspiana showed a bimodal size–frequency distribution, with immature and mature individuals found during the entire year. This pattern indicates continuous reproduction, with each cohort growing for at least three to four months and being responsible for two consecutive settlement peaks.

Type
Research Article
Copyright
Copyright © Marine Biological Association of the United Kingdom 2010

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

Benham, W.B. (1927) External sexual differences in the terebellid worms. Proceedings of the Zoological Society of London 1, 141148.CrossRefGoogle Scholar
Burnham, K.P. and Anderson, D.R. (2002) Model selection and multimodel inference: a practical information–theoretic approach. 2nd edition. New York: Springer.Google Scholar
Desrosiers, G., Vincent, B., Retière, C. and Boucher, L. (1988) Comparison de critères utilisables pour l'etude de la structure des populations du polychète Nereis virens (Sars). Canadian Journal of Zoology 66, 14541459.CrossRefGoogle Scholar
Ebert, T.A. and Russell, M.P. (1994) Allometry and Model II non-linear regression. Journal of Theoretical Biology 168, 367372.CrossRefGoogle Scholar
Florêncio, M.A.P. (2000) Dinâmica populacional e produção secundária de Laeonereis acuta (Treadwell, 1923) na Praia de Enseada dos Corais, Cabo de Santo Agostinho, Pernambuco, Brasil. Unpublished thesis. Federal University of Permanbuco, Recife, Brazil.Google Scholar
Garraffoni, A.R.S. and Amaral, A.C.Z. (2009) Postlarval development of Nicolea uspiana (Polychaeta: Terebellidae). Zoologia 26, 6166.CrossRefGoogle Scholar
Garraffoni, A.R.S. and Lana, P.C. (2008) Phylogenetic relationships within Terebellidae (Polychaeta: Terebelomorpha) based on morphological characters. Invertebrate Systematics 22, 605626.CrossRefGoogle Scholar
Giangrande, A. (1997) Polychaeta reproductive patterns, life cycles and life histories: an overview. Oceanography and Marine Biology: an Annual Review 35, 323386.Google Scholar
Gillet, P. and Gorman, E. (2002) Population structure and secondary production of Heteromastus filiformis (Polychaeta: Capitellidae) in the Loire estuary, France. Journal of the Marine Biological Association of the United Kingdom 82, 395402.CrossRefGoogle Scholar
Hurvich, C.M. and Tsai, C.L. (1989) Regression and time series model selection in small samples. Biometrika 76, 297307.CrossRefGoogle Scholar
Jolicoeur, P. (1990) Bivariate allometry: interval estimation of the slopes of the ordinary and standardized major axes and structural relationship. Journal of Theoretical Biology 144, 275285.CrossRefGoogle Scholar
Katsanevakis, S., Thessalou-Legaki, M., Karlou-Riga, C., Lefkaditou, C., Dimitriou, E. and Verriopoulos, G. (2007) Information–theory approach to allometric growth of marine organisms. Marine Biology 151, 949959.CrossRefGoogle Scholar
Lewis, J.B. (1998) Reproduction, larval development and functional relationships of the burrowing, spionid polychaeta Dipolydora armata with the calcareous hydrozoan Millepora complanata. Marine Biology 130, 651662.CrossRefGoogle Scholar
MacCord, F.S. (2005) Dinâmica populacional e biologia reprodutiva de duas espécies de Scolelepis (Spionidae) e de Laeonereis acuta (Nereididae) (Annelida: Polychaeta). Unpublished thesis. University of São Paulo, São Paulo, Brazil.Google Scholar
MacCord, F.S. and Amaral, A.C.Z. (2005) Morphometric analyses of two species of Scolelepis (Polychaeta: Spionidae). Journal of the Marine Biological Association of the United Kingdom 85, 829834.CrossRefGoogle Scholar
Manly, B.F.J. (1986) Multivariate statistical methods—a primer. London: Chapman & Hall.Google Scholar
Martin, J.P. and Bastida, R. (2006) Population structure, growth and production of Laeonereis culveri (Nereididae: Polychaeta) in tidal flats of Río de la Plata estuary, Argentina. Journal of the Marine Biological Association of the United Kingdom 86, 235244.CrossRefGoogle Scholar
McHugh, D. (1993) A comparative study of reproduction and development in the polychaeta family Terebellidae. Biological Bulletin. Marine Biological Laboratory, Woods Hole 185, 153167.CrossRefGoogle Scholar
Méndez, N., Romero, J. and Flos, J. (1997) Population dynamics and production of the polychaete Capitella capitata in the littoral zone of Barcelona (Spain, NW Mediterranean). Journal of Experimental Marine Biology and Ecology 218, 263284.CrossRefGoogle Scholar
Nogueira, J.M.M. (2003) A new species of Paraeupolymnia Young and Kritzler, 1986 (Polychaeta, Terebellidae, Terebellinae) from Brazil. Scientia Marina 67, 407413.Google Scholar
Omena, E.P. and Amaral, A.C.Z. (2000) Population dynamics and secondary production of Laeonereis acuta (Treadwell, 1923) (Nereididae: Polychaeta). Bulletin of Marine Science 67, 421431.Google Scholar
Omena, E.P. and Amaral, A.C.Z. (2001) Morphometric study of the nereidid Laeonereis acuta (Annelida: Polychaeta). Journal of the Marine Biological Association of the United Kingdom 81, 423426.CrossRefGoogle Scholar
Pagliosa, P.R. and Lana, P.C. (2000) Population dynamics and secondary production of Nereis oligohalina (Nereididae: Polychaeta) from a subtropical marsh in Southeast Brazil. Bulletin of Marine Science 67, 259268.Google Scholar
Preston, S.J. and Roberts, D. (2007) Variation in shell morphology of Calliostoma zizyphinum (Gastropoda: Trochidae). Journal of Molluscan Studies 73, 101104.CrossRefGoogle Scholar
Protopapas, N., Katsanevakis, S., Thessalou-Legaki, M. and Verriopoulos, G. (2007) Relative growth of the semi-terrestrial crab Pachygrapsus marmoratus: an information–theory approach. Scientia Marina 71, 383394.Google Scholar
Santos, P.J.P. (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, 657664.Google Scholar
Santos, P.J.P. (1994) Population dynamics and production of Scolelepis gaucha (Polychaeta: Spionidae) on the sandy beaches of southern Brazil. Marine Ecology Progress Series 110, 159165.CrossRefGoogle Scholar
Schroeder, P.C. and Hermans, C.O. (1975) Annelida: Polychaeta. In Giese, A.C. and Pearse, J.S. (eds) Reproduction of marine invertebrates, Volume 3. New York, San Francisco, London: Academic Press, pp. 1213.Google Scholar
Seitz, R.D. and Schaffner, L.C. (1995) Population ecology and secondary production of the polychaeta Loimia medusa (Terebellidae). Marine Biology 121, 701707.CrossRefGoogle Scholar
Shimizu, R.M. (1997) Ecologia populacional de Scolelepis squamata (Müller, 1806) (Polychaeta: Spionidae) e Callichirus major (Say, 1818) (Crustacea: Decapoda: Thalassinidae) da Praia de Barequeçaba (São Sebastião, SP). Unpublished thesis. University of São Paulo, São Paulo, Brazil.Google Scholar
Souza, J.R.B. and Borzone, C.A. (2000) Population dynamics and secondary production of Scolelepis squamata (Polychaeta: Spionidae) in an exposed sandy beach, southern Brazil. Bulletin of Marine Science 67, 221233.Google Scholar
Souza, J.R.B. and Borzone, C.A. (2007) Population dynamics and secondary production of Euzonus furciferus (Polychaeta: Opheliidae) in an exposed sandy beach of Southern Brazil. Revista Brasileira de Zoologia 24, 11391144.CrossRefGoogle Scholar
Warwick, R.M. and Price, R. (1975) Macrofauna production in an estuarine mud-flat. Journal of the Marine Biological Association of the United Kingdom 55, 118.CrossRefGoogle Scholar
Yokoyama, H. (1988) Effects of temperature on the feeding activity and growth rate of the spionid polychaete Paraprionospio sp. (form A). Journal of Experimental Marine Biology and Ecology 123, 4160.CrossRefGoogle Scholar
Yokoyama, H. (1990) Life history and population structure of the spionid polychaeta Paraprionospio sp. (form A). Journal of Experimental Marine Biology and Ecology 144, 125143.CrossRefGoogle Scholar
Zajac, R.N. (1991a) Population ecology of Polydora ligni (Polychaeta: Spionidae). I. Seasonal variation in population characteristics and reproductive activity. Marine Ecology Progress Series 77, 197206.CrossRefGoogle Scholar
Zajac, R.N. (1991b) Population ecology of Polydora ligni (Polychaeta: Spionidae). II. Seasonal demographic variation and its potential impact on life history evolution. Marine Ecology Progress Series 77, 207220.CrossRefGoogle Scholar