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Age, growth and reproduction of the protandrous hermaphrodite fish, Sarpa salpa, from the Portuguese continental coast

Published online by Cambridge University Press:  11 October 2016

Rafaela Barros Paiva ,
Ana Neves ,
Vera Sequeira ,
Ana Rita Vieira ,
Maria José Costa  and
Leonel Serrano Gordo
Rafaela Barros Paiva*
Affiliation:
MARE – Marine and Environmental Sciences Centre, Faculdade de Ciências da Universidade de Lisboa, Campo Grande, 1749–016 Lisboa, Portugal Departamento de Biologia Animal, Faculdade de Ciências da Universidade de Lisboa, Campo Grande, 1749–016 Lisboa, Portugal
Ana Neves
Affiliation:
MARE – Marine and Environmental Sciences Centre, Faculdade de Ciências da Universidade de Lisboa, Campo Grande, 1749–016 Lisboa, Portugal Departamento de Biologia Animal, Faculdade de Ciências da Universidade de Lisboa, Campo Grande, 1749–016 Lisboa, Portugal
Vera Sequeira
Affiliation:
MARE – Marine and Environmental Sciences Centre, Faculdade de Ciências da Universidade de Lisboa, Campo Grande, 1749–016 Lisboa, Portugal
Ana Rita Vieira
Affiliation:
MARE – Marine and Environmental Sciences Centre, Faculdade de Ciências da Universidade de Lisboa, Campo Grande, 1749–016 Lisboa, Portugal Departamento de Biologia Animal, Faculdade de Ciências da Universidade de Lisboa, Campo Grande, 1749–016 Lisboa, Portugal
Maria José Costa
Affiliation:
MARE – Marine and Environmental Sciences Centre, Faculdade de Ciências da Universidade de Lisboa, Campo Grande, 1749–016 Lisboa, Portugal
Leonel Serrano Gordo
Affiliation:
MARE – Marine and Environmental Sciences Centre, Faculdade de Ciências da Universidade de Lisboa, Campo Grande, 1749–016 Lisboa, Portugal Departamento de Biologia Animal, Faculdade de Ciências da Universidade de Lisboa, Campo Grande, 1749–016 Lisboa, Portugal
*
Correspondence should be addressed to: R.B. Paiva, MARE – Marine and Environmental Sciences Centre, Faculdade de Ciências da Universidade de Lisboa, Campo Grande, 1749–016 Lisboa, Portugal email: [email protected]
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Abstract

Salema, Sarpa salpa is a commercial exploited species in the Atlantic Ocean with little available information for the essential population parameters, such as age, growth and reproduction. The present study aims to describe these parameters for S. salpa obtained off the coast of Portugal. Ages were estimated from the whole otolith readings; the minimum and the maximum ages observed were 0 and 14 years, respectively, corresponding to 5.2 and 41.4 cm of total length (TL). Whole otolith readings and back-calculation approaches were used to estimate the parameters of the von Bertalanffy growth function and the Akaike's information criterion value suggested that the second approach was the best one to describe the growth of salema: L∞ = 45.07 cm, k = 0.14 year−1 and t0 = −1.43 year. The species is a protandric hermaphrodite and the sex change process occurred between 28.6 and 40.9 cm TL. A short spawning season was identified, extending from September to November. The estimated length at first maturity for males was 24.5 cm TL, corresponding to an age of 2 years at first maturity. This species exhibited a determinate fecundity type and the relative annual fecundity varied between 462 and 2662 oocytes per gram of gutted weight.

Keywords

Sarpa salpasalemaage estimationlength and age at first maturityspawning seasonfecundity
Type
Research Article
Information
Journal of the Marine Biological Association of the United Kingdom , Volume 98 , Issue 2 , March 2018 , pp. 269 - 281
Copyright
Copyright © Marine Biological Association of the United Kingdom 2016 

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References

REFERENCES

Akaike, H. (1973) Information theory and an extension of the maximum likelihood principle. In Petrov, B.N. and Csaki, F. (eds) 2nd International Symposium on Information Theory. Budapest: Akadémiai Kiadó, pp. 267–281.Google Scholar
Alonso-Fernández, A. (2011) Bioenergetics approach to fish reproductive potential: case of Trisopterus luscus (Teleostei) on the Galician Shelf (NW Iberian Peninsula) . PhD Thesis. University of Vigo, Spain, 352 pp.Google Scholar
Antolic, B., Skaramuca, B., Span, A., Musin, D. and Sanko-Njire, J. (1994) Food and feeding habits of a herbivore fish Sarpa salpa (L.) (Teleostei, Sparidae) in the southern Adriatic (Croatia). Acta Adriatica 35, 45–52.Google Scholar
Beamish, R.J. and Fourier, D.A. (1981) A method for comparing the precision of a set of age determinations. Canadian Journal of Fisheries and Aquatic Sciences 38, 982–983.CrossRefGoogle Scholar
Begg, G.A. (2005) Chapter 6: life history parameters. In Cadrin, S.X., Friedland, K.D. and Waldman, J.R. (eds) Stock identification methods, applications in fishery science. Cambridge, MA: Elsevier Academic Press, pp. 119–150.CrossRefGoogle Scholar
Bowker, A.H. (1948) A test for symmetry in contingency tables. Journal of the American Statistical Association 43, 572–574.CrossRefGoogle ScholarPubMed
Brown-Peterson, N.J., Wyanski, D.M., Saborido-Rey, F., Macewicz, B.J. and Lowerre-Barbieri, S.K. (2011) A standardized terminology for describing reproductive development in fishes. Marine and Coastal Fisheries: Dynamics, Management, and Ecosystem Science 3, 52–70.CrossRefGoogle 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, 197–242.CrossRefGoogle Scholar
Chang, W.Y.B. (1982) A statistical method for evaluating the reproducibility of age determination. Canadian Journal of Fisheries and Aquatic Sciences 39, 1208–1210.CrossRefGoogle Scholar
Criscoli, A., Colloca, F., Carpentieri, P., Belluscio, A. and Ardizzone, G. (2006) Observations on the reproductive cycle, age and growth of the salema, Sarpa salpa (Osteichthyes: Sparidae) along the western central coast of Italy. Scientia Marina 70, 131–138.CrossRefGoogle Scholar
DGRM (2015) Direcção Geral de Recursos Naturais, Segurança e Serviços Marítimos (General Directorate for Natural Resources, Safety and Maritime Services). Available at http://www.dgrm.mam.gov.pt (accessed 28 October 2015).Google Scholar
Dulčić, J. and Kraljević, M. (1996) Weight-length relationships for 40 fish species in the eastern Adriatic (Croatian waters). Fisheries Research 28, 243–251.CrossRefGoogle Scholar
Dulčić, J., Kraljevic, M., Grbec, B. and Pallaoro, A. (1997) Composition and temporal fluctuations of inshore juvenile fish populations in the Kornati Archipelago, eastern middle Adriatic. Marine Biology 129, 267–277.Google Scholar
El-Etreby, S.G., Ahmed, A.I., Alwany, M.A. and Ali, R.A. (2015) Reproductive biology of the Salema, fish Sarpa salpa (Osteichthyes: Sparidae) along the eastern coast of Libya. Egyptian Journal of Aquatic Biology and Fisheries 19, 83–94.Google Scholar
Falcón, J., Besseau, L., Fazzari, D., Attia, J., Gaildrat, P., Beauchaud, M. and Boeuf, G. (2003) Melatonin modulates secretion of growth hormone and prolactin by trout pituitary glands and cells in culture. Endocrinology 144, 4648–4658.CrossRefGoogle ScholarPubMed
FAO (2014) Food and Agriculture Organization of the United Nations: the state of world fisheries and aquaculture – opportunities and challenges. Rome: FAO, 243 pp.Google Scholar
Folkvord, A. and Mosegaard, H. (2002) Growth and growth analysis. In Panfili, J., Pontual, H., Troadec, H. and Wright, P. (eds) Manual of fish sclerochronology. Brest: Ifremer-IRD coedition, pp. 146–166.Google Scholar
Fowler, A.J. and Short, D.A. (1998) Validation of age determination from otoliths of the King George whiting Sillaginodes punctate (Perciformes). Marine Biology 130, 577–587.CrossRefGoogle Scholar
Francis, R.I.C.C. (1990) Back-calculation of fish length: a critical review. Journal of Fish Biology 36, 883–902.CrossRefGoogle Scholar
Froese, R. (2006) Cube law, condition factor and weight-length relationships: history, meta-analysis and recommendations. Journal of Applied Ichthyology 22, 241–253.CrossRefGoogle Scholar
Ganias, K., Lowerre-Barbieri, S. and Cooper, W. (2015) Understanding the determinate–indeterminate fecundity dichotomy in fish populations using a temperature dependent oocyte growth model. Journal of Sea Research 96, 1–10.CrossRefGoogle Scholar
Ganias, K., Murua, H., Claramunt, G., Dominguez-Petit, R., Gonçalves, P., Juanes, F., Keneddy, J., Klibansky, N., Korta, M., Kurita, Y., Lowerre-Barbieri, S., Macchi, G., Matsuyama, M., Medina, A., Nunes, C., Plaza, G., Rideout, R., Somarakis, S., Thorsen, A., Uriarte, A. and Yoneda, M. (2014) Egg production. In Domínguez-Petit, R., Murua, H., Saborido-Rey, F. and Trippel, E. (eds) Handbook of applied fisheries reproductive biology for stock assessment and management. Vigo: Digital CSIC. Available at http://hdl.handle.net/10261/87768 Google Scholar
Gerking, S.D. (1984) Assimilation and maintenance ration of an herbivorous fish, Sarpa salpa, feeding on a green alga. Transactions of the American Fisheries Society 113, 378–387.2.0.CO;2>CrossRefGoogle Scholar
Gordo, L.S. (1989) Age, growth and sexuality of sea bass, Dicentrarchus labrax (L.) from Aveiro lagoon, Portugal. Scientia Marina 53, 121–126.Google Scholar
Gordo, L.S., Costa, A., Abaunza, P., Lucio, P., Eltink, A.T.G.W. and Figueiredo, I. (2008) Determinate versus indeterminate fecundity in horse mackerel. Fisheries Research 89, 181–185.CrossRefGoogle Scholar
Greer-Walker, M., Witthames, P.R. and Bautista de los Santos, I. (1994) Is the fecundity of the Atlantic mackerel (Scomber scombrus: Scombridae) determinate? Sarsia 79, 13–26.CrossRefGoogle Scholar
Havelange, S., Lepoint, G., Dauby, P. and Bouquegneau, J. M. (1997) Feeding of the sparid fish Sarpa salpa in a seagrass ecosystem – diet and carbon flux. P.S.Z.N.J. Marine Ecology 18, 289–297.CrossRefGoogle Scholar
Hislop, J.R.G. and Hall, W.B. (1974) The fecundity of whiting, Merlangius merlangus (L.) in the North Sea, the Minch and at Iceland. Journal du Conseil/Conseil Permanent International pour l'Exploration de la Mer 36, 42–49.CrossRefGoogle Scholar
Hunter, J.R. and Macewicz, B.J. (1985) Rates of atresia in the ovary of captive and wild northern anchovy, Engraulis mordax . Fishery Bulletin 83, 119–136.Google Scholar
Hunter, J.R., Macewicz, B.J. and Kimbrell, C.A. (1989) Fecundity and other aspects of the reproduction of sablefish, Anoplopoma fimbria, in central California waters. CalCOFl Report 30, 61–72.Google Scholar
Hunter, J.R., Macewicz, B.J., Lo, N.C.H. and Kimbrel, C.A. (1992) Fecundity, spawning, and maturity of female Dover sole, Microstomus pacificus, with an evaluation of assumptions and precision. Fishery Bulletin 90, 101–128.Google Scholar
INE (2014) Statistical data for fisheries. Available at http://www.ine.pt (accessed 10 August 2015).Google Scholar
Jadot, C., Donnay, A., Acolas, M., Cornet, Y. and Bégout-Anras, M. (2006) Activity patterns, home-range size, and habitat utilization of Sarpa salpa (Teleostei: Sparidae) in the Mediterranean Sea. ICES Journal of Marine Science 63, 128–139.CrossRefGoogle Scholar
Joubert, C.S.W. (1981) Aspects of the biology of five species of inshore reef fishes on the Natal Coast, South Africa. Oceanographic Research Institute Investigational Report 51, 1–16.Google Scholar
Kjesbu, O.S., Witthames, P.R., Solemdal, P. and Greer-Walker, M. (1990) Ovulatory rhythm and a method to determine the stage of spawning in Atlantic cod (Gadus morhua). Canadian Journal of Fisheries and Aquatic Sciences 47, 1185–1193.CrossRefGoogle Scholar
Matić-Skoko, S., Kraljević, M., Dulčić, J. and Pallaoro, A. (2004) Growth of juvenile salema, Sarpa salpa (Teleostei: Sparidae), in the Kornati Archipelago, eastern Adriatic Sea. Scientia Marina 68, 411–417.CrossRefGoogle Scholar
Murua, H., Kraus, G., Saborido-Rey, F., Witthames, P.R., Thorsen, A. and Junquera, S. (2003) Procedures to estimate fecundity of marine fish species in relation to their reproductive strategy. Journal of Northwest Atlantic Fishery Science 33, 33–54.CrossRefGoogle Scholar
Murua, H. and Saborido-Rey, F. (2003) Female reproductive strategies of marine fish species of the North Atlantic. Journal of Northwest Atlantic Fishery Science 33, 23–31.CrossRefGoogle Scholar
Paiva, R.B., Neves, A., Sequeira, V., Vieira, A.R., Costa, M.J., Domingos, I. and Gordo, L.S. (2013) Age, growth and mortality of Pontinus kuhlii (Bowdich, 1825) (Scorpaeniformes: Scorpaenidae) in the Gorringe, Ampère, Unicorn and Lion seamounts. Scientia Marina 77, 95–104.CrossRefGoogle Scholar
Paiva, R.B., Neves, A., Vieira, A.R., Sequeira, V., Vendrell, C., Costa, M.J., Peleteiro, M. and Gordo, L.S. (2014) Cystic structures in fish ovaries: more common than we think. The case study of Sarpa salpa (Sparidae). Cybium 38, 158–160.Google Scholar
Pallaoro, A., Dulčić, J., Matić-Skoko, S., Kraljević, M. and Jardas, I. (2008) Biology of the salema, Sarpa salpa (L. 1758) (Pisces, Sparidae) from the middle-eastern Adriatic. Journal of Applied Ichthyology 24, 276–281.CrossRefGoogle Scholar
Pashkov, A.N. and Reshetnikov, S.I. (2012) First catch of salema Sarpa salpa (Perciformes, Sparidae) in waters of Russia. Journal of Ichthyology 52, 566–568.CrossRefGoogle Scholar
Ruitton, S., Francour, P. and Boudouresque, C.F. (2000) Relationships between algae, benthic herbivorous invertebrates and fishes in rocky sublittoral communities of a temperate sea (Mediterranean). Estuarine, Coastal and Shelf Science 50, 217–230.CrossRefGoogle Scholar
Russell, B., Pollard, D., Mann, B.Q., Buxton, C.D. and Carpenter, K.E. (2014) Sarpa salpa. In The IUCN red list of threatened species. Version 2015.2. Available at http://www.iucnredlist.org.Google Scholar
Sarkar, A. and Upadhyay, B. (2011) Influence of photoperiod and temperature on reproduction and gonadal maturation in goldfish: Carassius auratus . International Journal of Applied Biology and Pharmaceutical Technology 2, 352–358.Google Scholar
Schneider, C.A., Rasband, W.S. and Eliceiri, K.W. (2012) NIH Image to ImageJ: 25 years of image analysis. Nature Methods 9, 671–675.CrossRefGoogle ScholarPubMed
Tuset, V.M., González, J.I., Lozano, I.J. and García-Días, M.M. (2004) Age and growth of the backtail comber, Serranus atricauda (serranidae), off the Canary Islands (Central-Eastern Atlantic). Bulletin of Marine Science 74, 53–68.Google Scholar
Villamil, M.M., Lorenzo, J.M., Pajuelo, J.G., Ramos, A. and Coca, J. (2002) Aspects of the life history of the salema, Sarpa salpa (Pisces, Sparidae), off the Canarian Archipelago (central-east Atlantic). Environmental Biology of Fishes 63, 183–192.CrossRefGoogle Scholar
von Bertalanffy, L. (1938) A quantitative theory of organic growth (inquiries on growth laws II). Human Biology 10, 181–213.Google Scholar
Walt, B.A. and Beckley, L.E. (1997) Age and growth of Sarpa salpa (Pisces: Sparidae) off the east coast of South Africa. Fisheries Research 31, 241–248.CrossRefGoogle Scholar
Walt, B.A. and Mann, B.Q. (1998) Aspects of the reproductive biology of Sarpa salpa (Pisces: Sparidae) off the east coast of South Africa. South African Journal of Zoology 33, 241–248.CrossRefGoogle Scholar
Witthames, P.R. and Greer-Walker, M. (1995) Determinacy of fecundity and oocyte atresia in sole (Solea solea) from the Channel, the North Sea and Irish Sea. Aquatic Living Resources 8, 91–109.CrossRefGoogle Scholar
Wootton, R.J. (1992) Constraints in the evolution of fish life histories. Netherlands Journal of Zoology 42, 291–303.CrossRefGoogle Scholar
Zar, J.H. (1999) Biostatistical analysis. New York, NY: Prentice Hall, 663 pp.Google Scholar