Hostname: page-component-78c5997874-94fs2 Total loading time: 0 Render date: 2024-10-31T13:18:33.221Z Has data issue: false hasContentIssue false
  • English
  • Français

Comparative reproductive biology of Sciaenidae family species in the Río de la Plata and Buenos Aires Coastal Zone, Argentina

Published online by Cambridge University Press:  16 October 2012

M.I. Militelli ,
G.J. Macchi  and
K.A. Rodrigues
M.I. Militelli*
Affiliation:
Instituto Nacional de Investigación y Desarrollo Pesquero (INIDEP), Paseo Victoria Ocampo N° 1, CC.175, Mar del Plata (7600), Argentina Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), República Argentina
G.J. Macchi
Affiliation:
Instituto Nacional de Investigación y Desarrollo Pesquero (INIDEP), Paseo Victoria Ocampo N° 1, CC.175, Mar del Plata (7600), Argentina Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), República Argentina
K.A. Rodrigues
Affiliation:
Instituto Nacional de Investigación y Desarrollo Pesquero (INIDEP), Paseo Victoria Ocampo N° 1, CC.175, Mar del Plata (7600), Argentina Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), República Argentina
*
Correspondence should be addressed to: M.I. Militelli, Instituto Nacional de Investigación y Desarrollo Pesquero (INIDEP), Paseo Victoria Ocampo N° 1, CC.175, Mar del Plata (7600) email: militell@inidep.edu.ar
Get access Rights & Permissions [Opens in a new window]

Abstract

A comparative analysis on various aspects of the reproductive biology of 7 Sciaenidae family species was done. In addition the reproductive parameters needed for stock assessment models were provided. The research covered the analysis of the duration of the breeding season and the estimation of reproductive variables such as size at maturity, fecundity and spawning frequency. When all species were considered together, some aspects of reproduction were similar, regarding the reproductive strategy; all species are batch spawners with indeterminate fecundity and an extensive reproductive season (approximately six months) except for Pogonias cromis, which showed a more limited spawning season (three months). With regard to reproductive potential, wide differences in fecundity values mainly due to the different sizes attained by each species were observed (range in batch fecundity values between 5000 and 2,800,000 hydrated oocytes). However, when relative fecundity was compared, average values were generally similar, ranging approximately between 150 and 200 hydrated oocytes per female gram. Pogonias cromis is the exception within this group, because the mean relative fecundity ranged between 75 and 98 hydrated oocytes per ovary-free female gram. This difference may be a consequence of the greater oocyte size reached by P. cromis eggs (1100–1400 μm) compared to the rest of sciaenid analysed (750–900).

Keywords

Sciaenidaereproductive strategyreproductive potentiallength at first maturityfecundityspawning frequency
Type
Research Article
Information
Journal of the Marine Biological Association of the United Kingdom , Volume 93 , Special Issue 2: Fish and Fisheries , March 2013 , pp. 413 - 423
Copyright
Copyright © Marine Biological Association of the United Kingdom 2012

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

Acha, E.M., Mianzan, H., Lasta, C.A. and Guerrero, R.A. (1999) Estuarine spawning of whitemouth croaker Micropogonias furnieri (Pisces: Sciaenidae), in the Río de la Plata, Argentina. Marine and Freshwater Research 50, 57–65.Google Scholar
Aubone, A. and Wöhler, O.C. (2000) Aplicación del método de máxima verosimilitud a la estimación de parámetros y comparación de curvas de crecimiento de Von Bertalanffy. Serie INIDEP Informes Técnicos 37, 21.Google Scholar
Barbieri, L.R., Chittenden, M.E. Jr and Lowerre-Barbieri, S.K. (1994) Maturity, spawning, and ovarian cycle of Atlantic croaker, Micropogonias undulatus, in the Chesapeake Bay and adjacent coastal waters. Fishery Bulletin 92, 671–685.Google Scholar
Beacham, T.D. (1983) Growth and maturity of Atlantic cod (Gadus morhua) in the southern Gulf of St Lawrence. Canadian Technical Report of Fisheries and Aquatic Science 1142.Google Scholar
Brown-Peterson, N.J., Wyanski, D.M., Saborido-Rey, F. Macewicz, B.J. and Lowerre-Barbieri, S. (2011) A standardized terminology for describing reproductive development in fishes. Marine and Coastal Fisheries 3, 52–70.Google Scholar
Bumguardner, B.W., Colua, R.L., Young, E., Westbrook, D. and Buckley, R. (1995) Black drum life history in Texas Bays with emphasis on the Upper Laguna Madre. Texas Parks and Wildlife Department, Coastal Fisheries Division. Final Report for project F-36-R.Google Scholar
Carozza, C., Navarro, L., Jaureguizar, A., Lasta, C. and Bertolotti, M.I. (2001) Asociación íctica costera bonaerense 'Variado Costero'. Informe I. INIDEP Technical Report 48, 28 pp.Google Scholar
Cassia, M.C. (1986) Reproducción y fecundidad de la pescadilla de red (Cynoscion striatus). Publicación de la Comisión Técnica Mixta del Frente Marítimo 1, 191–203.Google Scholar
Cordo, H.D. (1986) Estudios biológicos sobre peces costeros con datos de dos campañas de investigación realizadas en 1981. IV. La pescadilla real (Macrodon ancylodon). Publicación de la Comisión Técnica Mixta del Frente Marítimo 1, 47–52.Google Scholar
Cousseau, M.B. (1985) Los peces del Río de la Plata y de su Frente Marítimo. In Yañez Arancibia, A. (ed.) Fish community ecology in estuaries and coastal lagoons: towards an ecosystem integration. DR (R) UNAM Press México, pp. 515–534.Google Scholar
Cousseau, M.B., Cotrina, C.P., Cordo, H.D. and Burgos, G.E. (1986) Análisis de datos biológicos de corvina rubia (Micropogonias furnieri) y pescadilla de red (Cynoscion striatus) obtenidos en dos campañas del año 1983. Publicación de la Comisión Técnica Mixta del Frente Marítimo 1, 319–332.Google Scholar
Díaz de Astarloa, J.M., Aubone, A. and Cousseau, M.B. (1999) Asociaciones ícticas de la plataforma costera de Uruguay y norte de Argentina, y su relación con los parámetros ambientales. Physis 57, 29–45.Google Scholar
Draper, N. and Smith, H. (1981) Applied regression analysis. 2nd edition. New York: John Wiley and Sons.Google Scholar
Fernández Aráoz, N.C., Lagos, N. and Carozza, C. (2005) Asociación ictica costera bonaerense ‘variado costero’ evolución de las capturas desembarcadas por la flota comercial argentina (1990–2003). INIDEP Technical Report 4, 21 pp.Google Scholar
García del Moral, R. (1993) Laboratorio de anatomía patológica. Madrid: McGraw-Hill and Ed. Interamericana.Google Scholar
Giannini, R. and Paiva-Filho, A.M. (1992) Aspectos da Bioecologia de Menticirrhus americanus (Teleostei, Sciaenidae) na Bahía de Santos, SP, Brasil. Boletim do Instituto de Pesca 19, 1–15.Google Scholar
Haimovici, M. (1982) Estructura y dinámica poblacional del pargo blanco Umbrina canosai (Sciaenidae, Pisces) del litoral de Rio Grande do Sul, Brasil. PhD thesis. Universidad Nacional de Buenos Aires, Facultad de Ciencias Exactas y Naturales, Buenos Aires, Argentina, 273 pp.Google Scholar
Harding, S.M. and Chittenden, M.E. Jr (1987) Reproduction, movements and population dynamics of the southern kingfish Menticirrhus americanus in the northwestern Gulf of Mexico. NOAA Technical Report NMFS 49, 1–21.Google Scholar
Hinckley, S. (1990) Variation of egg size of walleye pollock Theragra chalcogramma with a preliminary examination of the effect of egg size on larval size. Fishery Bulletin US 88, 471–483.Google Scholar
Hubold, G. (1978) Variations in growth rate and maturity of herring in the North Sea in the years 1955–1973. Rapports et Procès-Verbaux des Réunions du Conseil International pour l'Exploration de la Mer 172, 154–163.Google Scholar
Hunter, J.R. and Goldberg, S.R. (1980) Spawning incidence and batch fecundity in northern anchovy, Engraulis mordax . Fishery Bulletin US 77, 641–652.Google 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 US 83, 119–136.Google Scholar
Hunter, J.R., Lo, N.C.H. and Leong, R.J.H. (1985) Batch fecundity in multiple spawning fishes. In Lasker, R.M. (ed.) An egg production method for estimating spawning biomass of pelagics fish: application to the northern anchovy, Engraulis mordax. NOAA Technical Report NMFS 36, pp. 67–77.Google Scholar
Hunter, J.R., Macewicz, B.J. and Sibert, J.R. (1986) The spawning frequency of Skipjack Tuna, Katsuwonus pelamis, from the South Pacific. Fishery Bulletin US 84, 895–903.Google Scholar
Hunter, J.R., Macewicz, B.J., Lo, N.C.H. and Kimbrell, C.A. (1992) Fecundity, spawning, and maturity of female Dover sole Microstomus pacificus, with an evaluation of assumptions and precision. Fishery Bulletin US 90, 101–128.Google Scholar
Jaureguizar, A.J., Menni, R.C., Lasta, C.A. and Guerrero, R.A. (2006) Fish assemblages of the northern Argentine coastal system: spatial patterns and their temporal variations. Fisheries Oceanography 15, 326–344.Google Scholar
Juras, A.A. and Yamaguti, N. (1989) Sexual maturity, spawning and fecundity of king weakfish Macrodon ancylodon, caught off Rio Grande do Sul State (southern coast of Brazil). Boletim do Instituto Oceanográfico da USP 37, 51–58.CrossRefGoogle Scholar
Kendall, M.G. and Stuart, A. (1967) The advanced theory of statistics. London: Charles Griffin and Company Limited, 690 pp.Google Scholar
Kjesbu, O.S., Solemdal, P., Bratland, P. and Fonn, M. (1996) Variation in annual egg production in individual captive Atlantic cod (Gadus morhua). Canadian Journal of Fisheries and Aquatic Sciences 53, 610–620.CrossRefGoogle Scholar
Lewis, D. dos, S. and Fontoura, N.F. (2005) Maturity and growth of Paralonchurus brasiliensis females in southern Brazil (Teleostei, Perciformes, Sciaenidae). Journal of Applied Ichthyology 21, 94–100.Google Scholar
Macchi, G.J. (1998) Preliminary estimate of spawning frequency and batch fecundity of striped weakfish, Cynoscion striatus, in coastal waters off Buenos Aires province. Fishery Bulletin US 96, 375–381.Google Scholar
Macchi, G.J. and Acha, M.E. (1998) Aspectos reproductivos de las principales especies de peces en la Zona Común de Pesca Argentino–Uruguaya y en El Rincón. Noviembre 1994. In Lasta, C.A. (ed.) Resultados de una campaña de evaluación de recursos demersales costeros de la provincia de Buenos Aires y del Litoral Uruguayo. Noviembre 1994. INIDEP Technical Report 21, 67–89.Google Scholar
Macchi, G.J. and Christiansen, H.E. (1992) Estimación de la fecundidad de la corvina rubia (Micropogonias furnieri) mediante la aplicación del método estereométrico. Publicación de la Comisión Técnica Mixta del Frente Marítimo 12, 17–22.Google Scholar
Macchi, G.J., Acha, E.M and Lasta, C.A. (2002) Reproduction of black drum (Pogonias cromis) in the Río de la Plata estuary, Argentina. Fisheries Research 59, 83–92.Google Scholar
Macchi, G.J., Acha, E.M. and Militelli, M.I. (2003) Seasonal egg production pattern of whitemouth croaker (Micropogonias furnieri) of the Río de la Plata estuary, Argentina–Uruguay. Fishery Bulletin US 101, 332–342.Google Scholar
Macchi, G.J., Pájaro, M. and Ehrlich, M. (2004) Seasonal egg production pattern of the Patagonian stock of Argentine hake (Merluccius hubbsi). Fisheries Research 67, 25–38.Google Scholar
Militelli, M.I. (2007) Biología reproductiva comparada de especies de la familia Sciaenidae en aguas del Río de la Plata y Costa Bonaerense. PhD thesis. Universidad Nacional de Mar del Plata, Facultad de Ciencias Exactas y Naturales, Mar del Plata, Argentina, 145 pp.Google Scholar
Militelli, M.I. and Macchi, G.J. (2004) Spawning and fecundity of king weakfish, Macrodon ancylodon, in the Río de la Plata estuary, Argentina–Uruguay. Journal of the Marine Biological Association of the United Kingdom 84, 443–447.Google Scholar
Militelli, M.I. and Macchi, G.J. (2006) Spawning and fecundity of striped weakfish, Cynoscion guatucupa, in the Río de la Plata estuary and adjacent marine waters, Argentina–Uruguay. Fisheries Research 77, 110–114.Google Scholar
Murphy, M.D. and Taylor, R.G. (1989) Reproduction and growth of black drum, Pogonias cromis, in the Northeast Florida. Northeast Gulf Science 10, 127–137.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.Google Scholar
Nieland, D.L. and Wilson, C.A. (1993) Reproductive biology and annual variation of reproductive variables of black drum in the northern Gulf of Mexico. Transactions of the American Fisheries Society 122, 318–327.Google Scholar
Norbis, W. and Pagano, D. (1985) Aspectos biológicos de Macrodon ancylodon . Comunicación Preliminar Actas Jornadas de Zoología de Uruguay: 12–13.Google Scholar
Rico, M.R. (2000) La salinidad y la distribución espacial de la ictiofauna en el estuario del Río de la Plata. Tesis de Licenciatura. Facultad de Ciencias Exactas y Naturales, UNMdP, 74 pp.Google Scholar
Smith, J.W. and Wenner, C.A. (1985) Biology of the southern kingfish in the South Atlantic Bight. Transactions of the American Fishery Society 114, 356–366.Google Scholar
Tyler, C.R. and Sumper, J.P. (1996) Oocyte growth and development in teleosts. Reviews in Fish Biology and Fisheries 6, 287–318.Google Scholar
Trippel, E.A. (1995) Age at maturity as a stress indicator in fisheries. Bioscience 45, 759–771.Google Scholar
Vizziano, D. and Berois, N. (1990) Ciclo histológico del ovario de Macrodon ancylodon (Bloch & Shneider, 1801) (Teleostei: Sciaenidae). Biología Pesquera 19, 39–47.Google Scholar
Wootton, R.J. (1994) Life histories as sampling devices: optimum egg size in pelagic fishes. Journal of Fish Biology 45, 1067–1077.Google Scholar