Hostname: page-component-78c5997874-m6dg7 Total loading time: 0 Render date: 2024-11-04T21:52:21.738Z Has data issue: false hasContentIssue false

Population biology of shrimp Artemesia longinaris (Crustacea: Decapoda: Penaeidae) from the southern coast of Brazil

Published online by Cambridge University Press:  19 January 2010

Rogério Caetano da Costa*
Affiliation:
LABCAM, Departamento Ciências Biológicas—Faculdade de Ciências—UNESP, Bauru, SP, Brazil, Avenida Eng. Edmundo Carrijo Coube, s/n—Vargem Limpa, 17033-360, Brazil
Joaquim Olinto Branco
Affiliation:
Centro de Ensino em Ciências Tecnológicas da Terra e do Mar, UNIVALI. Caixa Postal 360, 88301-970, Itajaí, Santa Catarina, Brazil
Irecê Farina Machado
Affiliation:
Laboratório de Crustáceos Decapodos, Instituto de Oceanografia—Universidade Federal do Rio Grande—FURG, Km 8 Rio Grande (RS), 96201-900, Brazil
Bruno Ribeiro Campos
Affiliation:
Laboratório de Aqüicultura, Instituto de Oceanografia—Universidade Federal do Rio Grande—FURG, Km 8 Rio Grande (RS), 96201-900, Brazil
Marcelo Gentil Avila
Affiliation:
Centro de Ensino em Ciências Tecnológicas da Terra e do Mar, UNIVALI. Caixa Postal 360, 88301-970, Itajaí, Santa Catarina, Brazil
*
Correspondence should be addressed to: R. Caetano da Costa, LABCAM, Departamento Ciências, Biológicas—Faculdade de Ciências—UNESP, Bauru, SP, Brazil, Avenida Eng. Edmundo Carrijo Coube, s/n—Vargem Limpa, 17033-360, Brazil email: [email protected]

Abstract

Size at morphological sexual maturity, sex-ratio, and the seasonal variation in abundance of the shrimp Artemesia longinaris Bate, 1888 were assessed off Pinheira Beach, Palhoça, Santa Catarina southern Brazil. Shrimp were collected monthly from November 2003 through to October 2004, in two areas that are customarily used by local traditional fishermen (27°52′–27°51′S and 48°33′–48°29′W). Of the total of 1099 specimens measured, 23.93% were males and 76.07% females. Mean size at first maturity (LM50) was estimated as 56.38 mm total length (TL) for males, and 70.34 mm TL for females. Females were significantly larger than males. Abundance of juveniles varied seasonally. A high predominance of juveniles in the areas sampled occurred in winter for both sexes, and in spring for females. In the summer and autumn, we observed a decrease in juveniles in both areas, mainly, area II. We suggest that the differential migration pattern of sexes during the reproductive cycle was the principal reason for the larger catch of females. The classical paradigm of continuous reproduction at lower latitude, with increased seasonality of the breeding period at higher latitudes, seems to apply to this species.

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

Bauer, R.T. (1992) Testing generalizations about latitudinal variation in reproduction and recruitment patterns with sicyoniid and caridean shrimp species. Invertebrate Reproduction and Development 22, 193202.CrossRefGoogle Scholar
Branco, J.O. (2005) Biologia e pesca do camarão sete-barbas Xiphopenaeus kroyeri (Heller) (Crustacea, Penaeidae), na Armação do Itapocoroy, Penha, Santa Catarina, Brasil. Revista Brasileira de Zoologia 22, 10501062.CrossRefGoogle Scholar
Branco, J.O. and Verani, J.R. (1998a) Aspectos bioecológicos do camarão-rosa Penaeus brasiliensis Latreille (Natantia, Penaeidae) da Lagoa da Conceição, Florianópolis, Santa Catarina, Brasil. Revista Brasileira de Zoologia 15, 345351.CrossRefGoogle Scholar
Branco, J.O. and Verani, J.R. (1998b) Estudo populacional do camarão-rosa Penaeus paulensis Pérez Farfante (Natantia, Penaeidae) na Lagoa da Conceição, Santa Catarina, Brasil. Revista Brasileira de Zoologia 15, 353364.CrossRefGoogle Scholar
Branco, J.O. and Fracasso, H.A.A. (2004) Ocorrência e abundância da carcinofauna acompanhante na pesca do Camarão Sete-Barbas (Xiphopenaeus kroyeri Heller) (Crustácea, Decapoda), na Armação do Itapocory, Penha, SC, Brasil. Revista Brasileira de Zoologia 21, 295301.Google Scholar
Branco, J.O., Lunardon-Branco, M.J., Souto, F.X. and Guerra, C.R. (1999) Estrutura populacional do camarão sete-barbas Xiphopenaeus kroyeri (Heller, 1862), na foz do rio Itajaí-Açú, Itajaí, SC, Brasil. Brazilian Archives of Biology and Technology 42, 115126.CrossRefGoogle Scholar
Boschi, E.E. (1969) Estudio biológico pesquero del camarón Artemesia longinaris Bate de Mar del Plata. Boletín del Instituto Nacional de Investigación y Desarrollo Pesquero 18, 147.Google Scholar
Boschi, E.E. (1997) Las pesquerías de crustáceos decápodos en el litoral de la República Argentina. Investigaciones Marinas 25, 1940.CrossRefGoogle Scholar
Boschi, E.E. and Mistakidis, M. (1966) Resultados preliminares de las campañas de pesca exploratoria del langostino y el camarón en Rawson, 1962–1963. Carpas FAO Technical Report 6, 115.Google Scholar
Boschi, E.E. and Scelzo, M.A. (1977) Desarrollo larval y cultivo del camarón comercial de Argentina Artemesia longinaris Bate (Crustacea, Decapoda, Penaeidae). FAO—Pesca 159, 287327.Google Scholar
Castilho, A.L., Gavio, M.A., Costa, R.C., Boschi, E.E., Bauer, R. and Fransozo, A. (2007a) Latitudinal variation in population structure and reproductive pattern of the endemic South American shrimp Artemesia longinaris (Penaeoidea). Journal of Crustacean Biology 27, 548552.Google Scholar
Castilho, A.L., Costa, R.C., Fransozo, A. and Boschi, E.E. (2007b) Reproductive biology of the shrimp Artemesia longinaris Bate, 1888 (Crustacea, Decapoda, Penaeidae) in the northern Coast of São Paulo State, Brazil. Revista de Biologia Tropical 55, 3948.Google Scholar
Castilho, A.L., Pie, M.R., Fransozo, A., Pinheiro, A.P. and Costa, R.C. (2008a) The relationship between environmental variation and species abundance in shrimp communities (Crustacea: Decapoda: Penaeoidea) in south-eastern Brazil. Journal of the Marine Biological Association of the United Kingdom 88, 119123.CrossRefGoogle Scholar
Castilho, A.L., Furlan, M., Costa, R.C. and Fransozo, V. (2008b) Reproductive biology of the rock shrimp Sicyonia dorsalis (Decapoda, Penaeoidea) from the southeastern coast of Brazil. Invertebrate Reproduction and Development 52, 5968.CrossRefGoogle Scholar
Castilho, A.L., Costa, R.C., Fransozo, A. and Negreiros-Fransozo, M.A. (2008c) Reproduction and recruitment of the South American red shrimp, Pleoticus muelleri (Crustacea, Solenoceridae), from the southeastern coast of Brazil. Marine Biology Research 4, 361368.Google Scholar
Cha, K.H., Oh, C-W., Hong, S.Y. and Park, K.Y. (2002) Reproduction and population dynamics of Penaeus chinensis (Decapoda: Penaeidae) on the western coast of Korea, Yellow Sea. Fisheries Research 56, 2536.CrossRefGoogle Scholar
Christiansen, H.E. and Scelzo, M.A. (1971) Ciclo de maduración sexual y observaciones sobre la morfologia del aparato genital del camarón Artemesia longinaris Bate. Carpas 16, 122.Google Scholar
Costa, R.C. and Fransozo, A. (2004) Reproductive biology of the shrimp Rimapenaeus constrictus (Decapoda, Penaeidae) in the Ubatuba region of Brazil. Journal of Crustacean Biology 24, 274281.CrossRefGoogle Scholar
Costa, R.C., Fransozo, A., Melo, G.A.S. and Freire, F.A.M. (2003) Chave ilustrada para identificação dos camarões Dendrobranchiata do litoral norte do estado de São Paulo, Brasil. Biota Neotropica 3, 112, avaliable in http://www.biotaneotropica.org.br/v3n1.CrossRefGoogle Scholar
Costa, R.C., Fransozo, A., Castilho, A.L. and Freire, F.A.M. (2005) Annual, seasonal and spatial variation of abundance of the shrimp Artemesia longinaris (Decapoda, Penaeoidea) in a south-eastern region of Brazil. Journal of the Marine Biological Association of the United Kingdom 85, 107112.CrossRefGoogle Scholar
Costa, R.C., Fransozo, A., Freire, F.A.M. and Castilho, A.L. (2007) Abundance and ecological distribution of the ‘sete-barbas’ shrimp Xiphopenaeus kroyeri (Heller, 1862) (Decapoda, Penaeoidea) in three bays of the Ubatuba region, southeastern Brazil. Gulf and Caribbean Research 19, 3341.CrossRefGoogle Scholar
Costa, R.C., Lopes, M., Castilho, A.L., Fransozo, A. and Simões, S.M. (2008) Abundance and distribution of juveniles pink shrimps Farfantepenaeus spp. in a mangrove estuary and adjacent bay on the northern shore of São Paulo State, southeastern Brazil. Invertebrate Reproduction and Development 52, 5158.CrossRefGoogle Scholar
D'Incao, F., Valentini, H. and Rodrigues, L.F. (2002) Avaliação da pesca de camarões nas regiões Sudeste e Sul do Brasil. 1965–1999. Atlântica 24, 4962.Google Scholar
Dumont, L.F.C. and D'Incao, F. (2004) Estágios de desenvolvimento gonadal de fêmeas do camarão-barba-ruça (Artemesia longinaris—Decapoda: Penaeidae). Iheringia, Série Zoológica 94, 389393.CrossRefGoogle Scholar
Gavio, M.A. and Boschi, E.E. (2004) Biology of the shrimp Artemesia longinaris Bate, 1888 (Crustacea: Decapoda: Penaeidae) from Mar del Plata coast, Argentina. Nauplius 12, 8394.Google Scholar
Kevrekidis, K. and Thessalou-Legaki, M. (2006) Catch rates, size structure and sex ratio of Melicertus kerathurus (Decapoda: Penaeidae) from an Aegean Sea trawl fishery. Fisheries Research 80, 270279.CrossRefGoogle Scholar
Nascimento, P.A.M. (1981) Variações no tamanho médio de maturação em Artemesia longinaris Bate, 1888 (Crustacea, Decapoda, Penaeidae). Naturalia 6, 3342.Google Scholar
Rodriguez, M., Gómez, M., Verdi, A. and Muniz, P. (2002) Presencia de Artemesia longinaris (BATE, 1888) y peisos petrunkevitchi (BURKENROAD, 1945) (Crustacea, Decapoda) en aguas de baja salinidad en la costa de Montevideo. Boletín de la Sociedad Zoológica del Uruguay 13, 2124.Google Scholar
Semensato, X.E.G. and Di Beneditto, A.P.M. (2008) Population dynamic and reproduction of Artemesia longinaris (Decapoda: Penaeidae) in Rio de Janeiro State, south-eastern Brazil. Boletim do Instituto de Pesca 34, 8998.Google Scholar
Vazzoler, A.E.A.M. (1996) Biologia da reprodução de peixes teleósteos: teoria e prática. Maringá: Editora Eduem.Google Scholar
Zar, T.H. (1984) Biostatistical analysis. New Jersey: Prentice-Hall Inc.Google Scholar