Hostname: page-component-586b7cd67f-2plfb Total loading time: 0 Render date: 2024-11-23T00:45:18.791Z Has data issue: false hasContentIssue false

Demography of the Agassiz's parrotfish Sparisoma frondosum (Agassiz, 1831) in north-eastern Brazil

Published online by Cambridge University Press:  08 July 2015

Rosângela Lessa*
Affiliation:
Departamento de Pesca e Aqüicultura (DEPAq), Universidade Federal Rural de Pernambuco (UFRPE), Dois Irmãos, 52171-900 Recife, PE, Brazil Programa de Pós-Graduação em Biologia Animal, Universidade Federal de Pernambuco (UFPE), Cidade Universitária, Recife, PE, Brazil
Camila R. Da Silva
Affiliation:
Programa de Pós-Graduação em Biologia Animal, Universidade Federal de Pernambuco (UFPE), Cidade Universitária, Recife, PE, Brazil
June F. Dias
Affiliation:
Instituto Oceanográfico (IO), Universidade de São Paulo (USP), Praça do Oceanográfico, 191, 05508-120 São Paulo, SP, Brazil
Francisco M. Santana
Affiliation:
Unidade Acadêmica de Serra Talhada (UAST), Universidade Federal Rural de Pernambuco (UFRPE), Serra Talhada, 56903-970 PE, Brazil
*
Correspondence should be addressed to:R. Lessa, Departamento de Pesca e Aqüicultura (DEPAq), Universidade Federal Rural de Pernambuco (UFRPE), Dois Irmãos, 52171-900 Recife, PE, Brazil email: [email protected]

Abstract

Age and growth of Agassiz's parrotfish Sparisoma frondosum captured off Brazil (Pernambuco) were estimated using sagittal otoliths from 251 specimens. Sex of each specimen was determined and showed that 130 specimens were females (13.1 to 36.8 cm TL) and 121 were males (17.5 to 36.6 cm TL). The otolith marginal increment analysis indicated a single translucent ring formed every year. Parameters of growth curves were derived for the von Bertalanffy (VBGF) and Gompertz models. Based on the Akaike information criterion (AIC), both models were suitable for describing the growth of this species. VBGF parameters were estimated for males L = 39.74 cm TL, K = 0.22, t 0 = −1.63 years, females L = 32.38 cm TL, K = 0.44; t 0 = −0.23 years; and for the sexes combined L = 33.66 cm TL, K = 0.41, t 0 = −0.27 years. The study showed that 55% of individuals were 3 and 4 years of age, with maximal age of 9 years. Mature females (>17.6 cm TL) accounted for 45% of the sample. The age at first maturity for females was 1.6 years. For males the size at first maturity was not determined as immature individuals were not present in the overall sample. Also, primary males (PM) and specimens with gonads undergoing sexual transition were not found. The age structure and growth parameters for S. frondosum are an important contribution to the assessment of the state of exploitation of this species.

Type
Research Article
Copyright
Copyright © Marine Biological Association of the United Kingdom 2015 

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

Akaike, H. (1974) A new look at the statistical model identification. IEEE Transactions on Automatic Control 19, 716723.Google Scholar
Alonso-Fernández, A., Alós, J., Gran, A., Domingues-Petit, R. and Saborido-Rey, F. (2011) The use of histological techniques to study the reproductive biology of the hermaphroditic Mediterranean fishes Coris julis, Serranus scriba and Diplodus annularis. Special Section: Fisheries Reproductive Biology. Marine and Coastal Fisheries: Management and Ecosystem Science, American Fisheries Society 3, 145159.Google Scholar
Bannerot, S.P. (1984) The Dynamics of Exploited Groupers (Serranidae): an investigation of the Protogynous Hermaphroditic Reproductive Strategy . PhD dissertation, University of Miami, FL.Google Scholar
Beamish, R.J. and Fournier, D.A. (1981) A method for comparing the precision of a set of age determinations. Canadian Journal of Fisheries and Aquatic Sciences 38, 982983.Google Scholar
Brazil, Ministério do Meio Ambiente. Portarias No. 445, de 17 de Dezembro de 2014, Diário Oficial da União–Seção 1, 245, 110 (18 December 2014); http://pesquisa.in.gov.br/imprensa/jsp/visualiza/index.jsp?data=18/12/2014&jornal.Google Scholar
Burnham, K.P. and Anderson, D.R. (2002) Model selection and multimodel inference. A practical information – theoretical approach, 2nd edn. New York, NY: Springer.Google Scholar
Cadvallader, P.L. (1978) Age, growth and condition of common river galaxias, Galaxias vulgaris Stolkell, in the Glentni river, Canterbury, New Zealand. Fishery Research Bulletin 17, 1520.Google Scholar
Campana, S.E. (2001) Accuracy, precision and quality control in age determination, including a review of the use and abuse of age validation methods. Journal of Fish Biology 59, 197242.Google Scholar
Cheung, W.W.L., Pitcher, T.J. and Pauly, D. (2005) A fuzzy logic expert system to estimate intrinsic extinction vulnerabilities of marine fishes to fishing. Biological Conservation 124, 97111.CrossRefGoogle Scholar
Choat, J.H. and Robertson, D.R. (2002) Age-based studies. In Sale, P.F. (ed.) Coral reef fishes. Dynamics and diversity in a complex ecosystem. New York, NY: Academic Press, pp. 5780.Google Scholar
Choat, J.H., Robertson, D.R., Ackerman, J.L. and Posada, J.M. (2003) An age-based demographic analysis of the Caribbean spotlight parrotfish Sparisoma viridae . Marine Ecology Progress Series 246, 265277.CrossRefGoogle Scholar
Collins, A.B. and McBride, R.S. (2011) Demographics by depth: spatially explicit life-history dynamics of a protogynous reef fish. Fishery Bulletin 109, 232242.Google Scholar
Crabtree, R.E., Harnden, C.W., Snodgrass, D. and Stevens, C. (1996) Age, growth, and mortality of bonefishes, Albula vulpes, from the waters of the Florida Keys. Fishery Bulletin 94, 442451.Google Scholar
Francis, R.C. (1992) Sexual lability in teleosts: developmental factors. Quarterly Review of Biology, 67, 117.Google Scholar
Freitas, R., Osmar, J.L., Silva, P.N., Floeter, S.R., Bernardi, G. and Ferreira, C.E.L. (2014) The occurrence of Sparisoma frondosum (Teleostei: Labridae) in the Cape Verde Archipelago with a summary of expatriated Brazilian endemic reef fishes. Marine Biodiversity 44, 173179.Google Scholar
Gompertz, B. (1825) On the nature of the function expressive of the law of human mortality and on a new method of determining the value of life contingencies. Philosophical Transactions of the Royal Society of London 115, 513585.Google Scholar
Hastings, P.A. (1981) Gonad morphology and sex succession in the protogynous hermaphrodite Hemanthias vivanus (Jordan and Swain). Journal of Fish Biology 18, 443454.Google Scholar
Hewitt, D.A. and Hoenig, J.M. (2005) Comparison of two approaches for estimating natural mortality based on longevity. Fishery Bulletin 103, 433437.Google Scholar
Hixon, M.A., Johnson, D.W. and Sogard, S.M. (2014) BOFFFFs: on the importance of conserving old-growth age structure in fishery populations. ICES Journal of Marine Science 71, 21712185.CrossRefGoogle Scholar
IBAMA (2005) Boletim estatístico da pesca marítima e estuarina do Nordeste do Brasil- 2004. ESTATPESCA/Centro de Pesquisa e Gestão de Recursos Pesqueiros do Litoral Nordeste Tamandaré, PE: CEPENE, 152 pp.Google Scholar
Jonna, R. (2003) “Scaridae” Animal Diversity Web. Available at http://animaldiversity.ummz.umich.edu/site/accounts/information/Scaridae.html (last accessed 4 May 2013).Google Scholar
King, M. (1995) Fisheries biology, assessment and management. Oxford: Blackwell Science.Google Scholar
Kume, G., Kubo, Y., Yoshimura, T., Kiriyama, T. and Yamaguchi, A. (2010) Life history characteristics of the protogynous parrotfish Calotomus japonicus from northwest Kyushu, Japan. Ichthyological Research 57, 113120.Google Scholar
Lessa, R. and Araújo, B.M. (2009) Resultados: Séries históricas. In Lessa, R., Bezerra, J.L. Jr and Nóbrega, M.F. (eds) Dinâmica das frotas pesqueiras da Região Nordeste do Brasil. Fortaleza, Brazil: Martins & Cordeito LTDA, pp. 3558.Google Scholar
Longhurst, A.R. and Pauly, D.E. (1987) Ecology of tropical oceans. San Diego, CA: Academic Press.Google Scholar
Lou, D.C. (1992) Validation of annual growth bands in the otolith of tropical parrotfishes (Scarus schlegeli Bleeker). Journal of Fish Biology 41, 775790.CrossRefGoogle Scholar
Moura, R.L., Figueiredo, J.L. and Sazima, I. (2001) A new parrotfish (Scaridae) from Brazil, and revalidation of Sparisoma amplum (Ranzani, 1842), Sparisoma frondosum (Agassiz, 1831), Sparisoma axillare (Steindachner, 1878) and Scarus trispinosus (Valenciennes, 1840). Bulletin of Marine Science 68, 505524.Google Scholar
Muñoz, R.C. and Warner, R.R. (2003) A new version of the size-advantage hypothesis for sex change: incorporating sperm competition and size–fecundity skew. American Naturalist 161, 749761.Google Scholar
Nelson, J.S. (2006) Fishes of the world, 4th edn. New York, NY: John Wiley and Sons.Google Scholar
Padovani-Ferreira, B., Rocha, L.A., Ferreira, C.E., Francini-Filho, R., Moura, R., Gaspar, A.L., Feitosa, C., Choat, J.H., Myers, R. and Russell, B. (2012) Sparisoma frondosum. The IUCN Red List of Threatened Species. Version 2014.2. Available at www.iucnredlist.org (last accessed 27 July 2014).Google Scholar
Panfili, J., de Pontual, H., Troadec, H. and Wright, P.J. (2002) Manual of fish sclerochronology. Brest: IFREMER-IRD Coedition.Google Scholar
Pauly, D., Christensen, V., Dalsgaard, J., Froese, R. and Torres, F. Jr (1998) Fishing down marine food webs. Science 279, 860863.CrossRefGoogle ScholarPubMed
Petersen, C.W. and Warner, R.R. (2002) The ecological context of reproductive behavior. In Sale, P.F. (ed.) Coral reef fishes: dynamics and diversity in a complex ecosystem. New York, NY: Academic Press, pp. 103118.CrossRefGoogle Scholar
Reinboth, R. (1967) Diandric Teleost species. General and Comparative Endrocrinology 9, abstract 146.Google Scholar
Ribeiro, F.P. (2004) Composição da biocenose e abundância relativa de peixes capturados com covos nos Estados do Rio Grande do Norte e Pernambuco (BRASIL). Boletim Técnico Científico do CEPENE 12, 115128.Google Scholar
Robertson, D.R. and Warner, R.R. (1978) Sexual patterns in the labroid fishes of the western Caribbean. II. The parrotfishes (Scaridae). Smithsonian Contributions to Zoology 255, 126.Google Scholar
Robertson, R.D., Karg, F., Moura, R.L., De Victor, B.V. and Bernardi, G. (2006) Mechanisms of speciation and faunal enrichment in Atlantic parrotfishes. Molecular Phylogenetics and Evolution 40, 795807.Google Scholar
Sadovy de Mitcheson, Y. and Liu, M. (2008) Functional hermaphroditism in teleosts. Fish and Fisheries 9, 143.Google Scholar
Sadovy, Y. and Colin, P.L. (1995) Sexual development and sexuality in the Nassau grouper. Journal of Fish Biology 46, 961976.CrossRefGoogle Scholar
Sadovy, Y. and Shapiro, D.Y. (1987) Criteria for the diagnoses of hermaphroditism in fishes. Copeia 1987, 136156.Google Scholar
Shapiro, D.Y. (1987) Differentiation and evolution of sex change in fishes: a coral reef fish's social environment can control its sex. BioScience 37, 490497.Google Scholar
Shapiro, D.Y., Sadovy, Y. and McGehee, M.A. (1993) Periodicity of sex change and reproduction in the red hind, Epinephelus guttatus, a protogynous grouper. Bulletin of Marine Science 53, 11511162.Google Scholar
Sparre, P. and Venema, S.C. (1997) Introdução à avaliação de mananciais de peixes tropicais. Rome: FAO Documento técnico sobre as pescas, No. 306/1.Google Scholar
Takada, M. and Tachihara, K. (2009) Comparisons of age, growth, and maturity between male and female, and diploid and triploid individuals in Carassius auratus from Okinawa-jima Island, Japan. Aquatic Conservation: Marine and Freshwater Ecosystems 19, 806814.Google Scholar
Taylor, B.M. (2014) Drivers of protogynous sex change differ across spatial scales. Proceedings of the Royal Society B 281: 20132423. http://dx.doi.org/10.1098/rspb.2013.2423.Google Scholar
Vaske, T. Jr, Lessa, R.P.T., Ribeiro, A.C.B., de Nóbrega, M.F., Pereira, A. de A. and de. Andrade, C.D.P. (2006) A pesca comercial de peixes pelágicos no Arquipélago de São Pedro e São Paulo, Brasil. Tropical Oceanography 34, 3141.Google Scholar
Véras, D.P. (2008) Biologia reprodutiva dos budiões-batata, Sparisoma axillare e Sparisoma frondosum (Actinopterygii: Scaridae), capturados na costa central do estado de Pernambuco . MSc dissertation. Universidade Federal Rural de Pernambuco, Recife, Brazil.Google Scholar
von Bertalanffy, L. (1938) A quantitative theory of organic growth (inquiries on growth laws). Human Biology 10, 181213.Google Scholar
Warner, R.R. (1984) Mating behaviour and hermaphroditism in coral reef fishes: the diverse forms of sexuality found among tropical marine fishes can be viewed as adaptations to their equally diverse mating systems. American Scientist 72, 128136.Google Scholar
Westneat, M.W. & Alfaro, M.E. (2005) Phylogenetic relationships and evolutionary history of the reef fish family Labridae. Molecular Phylogenetics and Evolution 36, 370390.CrossRefGoogle ScholarPubMed
Zar, J.H. (1999) Biostatistical analysis, 4th edn. Upper Saddle River, NJ: Prentice Hall.Google Scholar