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Ontogenetic niche feeding partitioning in juvenile of white sea catfish Genidens barbus in estuarine environments, southern Brazil

Published online by Cambridge University Press:  01 August 2008

Manuel Mendoza-Carranza  and
João Paes Vieira
Manuel Mendoza-Carranza*
Affiliation:
El Colegio de la Frontera Sur—ECOSUR, Sistemas de Producción Alternativos, Pesquerías Artesanales Apartado Postal 1042, Admon. de Correos Tabasco, 2000, Calle Planetario Sin Número Esquina Con Circuito 86031, Villahermosa, Tabasco, México
João Paes Vieira
Affiliation:
Laboratório de Ictiologia, Departamento de Oceanografia, Fundação Universidade Federal do Rio Grande, Avenida Itália Km 8, Caixa Postal 474, Rio Grande—RS—Brazil
*
Correspondence should be addressed to: Manuel Mendoza-Carranza, El Colegio de la Frontera Sur—ECOSUR, Sistemas de Producción Alternativos, Pesquerías Artesanales Apartado Postal 1042, Admon. de Correos, Tabasco 2000, Calle Planetario Sin Número Esquina Con Circuito 86031, Villahermosa, Tabasco, México email: [email protected]
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Abstract

Ontogenetic diet changes (prey species richness and size) in juveniles of white sea catfish (Genidens barbus) were tested in three southern Brazilian estuaries: Mampituba (29°12′S), Tramandaí (30°02′S), Chuí (33°44′S). Cluster analysis revealed that white sea catfish juvenile populations in the three estuaries are composed of two feeding groups. These two feeding groups are coincident with a bimodal size–age distribution of the juveniles of white sea catfish. In small catfish (5 to 10 cm TL) copepods were the most numerous prey (Chuí = 86.66%N, Tramandaí = 85.52%N and Mampituba = 52.34%N). In large catfish (10 to 20 cm TL) the most abundant and frequent prey was fish (Chuí: 73.19%N and 74.56%FO; Tramandaí: 85.92%N and 73.33%FO; Mampituba: 52.34%N and 61.54%FO). The Morisita overlap index among small and large fish was low in all estuaries; high values of Morisita's similarity index were observed among same size catfish groups. In all cases, no differences were observed among prey bio-volume curves of same size predator groups (small, F = 0.41, P = 0.65; large, F = 2.19, P = 0.11). In all estuaries, prey size increased significantly with increasing predator size. The 90th regression quantile estimated with most precision the predator–prey size relationship.

Keywords

trophic ecologydiet overlapprey sizepredator–prey relationship
Type
Research Article
Information
Journal of the Marine Biological Association of the United Kingdom , Volume 89 , Issue 4 , June 2009 , pp. 839 - 848
Copyright
Copyright © Marine Biological Association of the United Kingdom 2008

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References

REFERENCES

Adriaens, D., Aerts, P. and Verraes, W. (2001) Ontogenetic shift in mouth opening mechanisms in a catfish (Clariidae, Siluriformes): a response to increasing functional demands. Journal of Morphology 247, 197–216.3.0.CO;2-S>CrossRefGoogle Scholar
Araújo, F.G. (1984) Hábitos alimentares de três bagres marinhos (Ariidae) no estuário da Lagoa dos Patos (RS), Brasil. Atlântica 7, 47–63.Google Scholar
Araújo, M.S., Bolnick, D.I., Machado, G., Giaretta, A.A. and Reis, S.F. (2007) Using δ13C stable isotope to quantify individual-level diet variation. Oecologia 152, 643–654.CrossRefGoogle ScholarPubMed
Asmus, M.L. (1996) Coastal plain and Patos Lagoon. In Seeliger, U., Odebrecht, C. and Castello, J.P. (eds) Subtropical convergence environments, the coast and sea in the south-western Atlantic. Berlin: Springer, pp. 9–12.Google Scholar
Bock, H.H. (2005) On some significance tests in cluster analysis. Journal of Classification 2, 77–108.CrossRefGoogle Scholar
Buckel, J. and McKown, K.A. (2002) Competition between juvenile striped bass and bluefish: resource partitioning and growth rate. Marine Ecology Progress Series 234, 191–204.CrossRefGoogle Scholar
Cade, B.S. and Noon, B.R. (2003) A gentle introduction to quantile regression for ecologists. Frontiers in Ecology and the Environment 1, 412–420.CrossRefGoogle Scholar
Cade, B.S., Noon, B.R. and Flather, C.H. (2005) Quantile regression reveals hidden bias and uncertainty in habitat models. Ecology 86, 786–800.CrossRefGoogle Scholar
Capitoli, R.R. (1992) Métodos para estimar volumes do conteúdo alimentar de peixes e macroinvertebrados. Atlântica, Rio Grande 4, 117–120.Google Scholar
Chaves, P.T.C. and Vendel, A.L. (1996) Aspectos da alimentação de Genidens genidens (VALENCIENNES) (SILURIFORMES, ARIIDAE) na Baía de Garatuba, Paraná. Revista Brasileira de Zoologia 13, 669–675.CrossRefGoogle Scholar
Chao, L.N., Pereira, L.E. and Vieira, J.P. (1985) Estuarine fish community of the Patos Lagoon (Lagoa dos patos, RS) Brasil. A baseline study. In Yáñez-Arancibia, A. (ed.) Fish community ecology in estuaries and coastal lagoons. Towards an ecosystem integration. México: Universidad Nacional Autónoma de México, pp. 429–450.Google Scholar
Cook, A. (1996) Ontogeny of feeding morphology and kinematics in juvenile fishes: a case study of the cottid fish Clinocottus analis. Journal of Experimental Biology 199, 1961–1971.CrossRefGoogle ScholarPubMed
Crow, M.E. (1982) Some statistical techniques for analyzing the stomach contents of fish. In Cailliet, G.M. and Simenstad, C.A. (eds) Gutshop'81, fish food habits studies. Proceedings of the Third Pacific Workshop, Pacific Grove, CA, 6–9 December 1981. Washington: Washington Sea-Grant Publications, pp. 8–15.Google Scholar
Denny, C.M. and Schiel, D.R. (2001) Feeding ecology of the banded wrasse Notolabrus fucicola (Labridae) in southern New Zealand: prey items, seasonal differences, and ontogenetic variation. New Zealand Journal of Marine and Freshwater Research 35, 925–33.CrossRefGoogle Scholar
Dopman, E.B., Sword, G.A. and Hillis, D.M. (2002) The importance of the ontogenetic niche in resource-associated divergence: evidence from a generalist grasshopper. Evolution 56, 731–740.Google ScholarPubMed
Efron, B. and Tibshirani, R. (1993) An introduction to the bootstrap. New York: Chapman and Hall.CrossRefGoogle Scholar
Eggold, B.T. and Motta, P.J. (1992) Ontogenetic dietary shifts and morphological correlates in striped mullet, Mugil cephalus. Environmental Biology of Fishes 34, 139–158.CrossRefGoogle Scholar
Floeter, J. and Temming, A. (2003) Explaining diet composition of North Sea cod (Gadus morhua): prey size preferences vs. prey availability. Canadian Journal of Fisheries and Aquatic Sciences 60, 140–150.CrossRefGoogle Scholar
Galarowicz, T.L., Adams, J.A. and Wahl, D.H. (2006) The influence of prey availability on ontogenetic diet shifts of a juvenile piscivore. Canadian Journal of Fisheries and Aquatic Sciences 63, 1722–1733.CrossRefGoogle Scholar
Garcia, A.M., Vieira, J.P. and Winemiller, K.O. (2001) Dynamics of the shallow-water fish assemblage of the Patos Lagoon estuary (Brazil) during cold and warm ENSO episodes. Journal of Fish Biology 59, 1218–1238.Google Scholar
Garcia, A.M., Vieira, J.P. and Winemiller, K.O. (2003) Effects of 1997–1998 El Niño on the dynamics of the shallow water fish assemblage of the Patos Lagoon estuary (Brazil). Estuarine, Coastal and Shelf Science 57, 489–500.CrossRefGoogle Scholar
Gelwick, F.P. (1990) Longitudinal and temporal composition of riffle and pool fish assemblages in a northeastern Oklahoma Ozark stream. Copeia 4, 1072–1082.CrossRefGoogle Scholar
Gould, W. (1992) Quantile regression with bootstrapped standard errors. Stata Technical Bulletin 9, 19–21.Google Scholar
Hall, S.J., Raffaelli, D., Basford, D.J., Robertson, M.R. and Fryer, R. (1990) The feeding relationship of the larger fish species in a Scottish Sea Loch. Journal of Fish Biology 37, 775–791.CrossRefGoogle Scholar
Higuichi, H., Reis, E.G. and Araújo, F.G. (1982) Uma nova espécie de bagre marinho do litoral do Rio Grande do Sul e considerações sobre o gênero nominal Netuma Bleeker, 1858 no Atlântico sul ocidental (Siluriformes, Ariidae). Atlântica 5, 1–15.Google Scholar
Hoese, H.D. (1966) Ectoparisitism by juvenile sea catfish, Galeichthys felis. Copeia 1996, 880–881.CrossRefGoogle Scholar
Hyslop, E.J. (1980) Stomach contents analysis: a review of methods and their application. Journal of Fish Biology 17, 411–429.CrossRefGoogle Scholar
Kelly, J.F. (2000) Stable isotopes of carbon and nitrogen in the study of avian and mammalian trophic ecology. Canadian Journal of Zoology 78, 1–27.CrossRefGoogle Scholar
Krebs, C.J. (1989) Ecological methodology. New York: Harper and Row Publishers.Google Scholar
Livingston, R.J. (1988) Inadequacy of species-level designations for ecological studies of coastal migratory fishes. Environmental Biology of Fishes 22, 225–234.CrossRefGoogle Scholar
Livingston, R.J. (2003) Trophic organization in coastal systems. New York: CRC Press.Google Scholar
Labropoulou, M. and Eleftheriou, A. (1997) The foraging ecology of two pairs of congeneric demersal fish: importance of morphological characteristics in prey selection. Journal of Fish Biology 50, 324–340.CrossRefGoogle Scholar
Ludwig, J.A. and Reynolds, J.F. (1988) Statistical ecology: a primer on methods and computing. New York: John Wiley & Sons, Inc.Google Scholar
Mendoza-Carranza, M. and Vieira, J.P. (2008) Whitemouth croaker Micropogonias furnieri (Desmarest, 1823) feeding strategies across four southern Brazilian estuaries. Aquatic Ecology 42, 83–93.CrossRefGoogle Scholar
Menezes, N.A. and Figueiredo, J.L. (1980) Manual de peixes marinhos do sudeste do Brasil. IV. Teleostei (3). São Paulo: Museu de Zoologia. Universidade de São Paulo.Google Scholar
Pereira, L.E., Ramos, L.A. and Pontes, S.X. (1998) Lista comentada dos peixes e crustáceos decápodos do estuário do Arroio Chuí e região costeira adjacente, RS. Atlântica 20, 165–172.Google Scholar
Petrik, R. and Levin, P. (2000) Estimating relative abundance of seagrass fishes: a quantitative comparison of three methods. Environmental Biology of Fishes 58, 461–466.CrossRefGoogle Scholar
Polis, G.A. (1984) Age structure components of niche width and intraspecific resource partitioning: can age function as ecological species? American Naturalist 123, 541–564.CrossRefGoogle Scholar
Ramos, L.A. and Vieira, J.P. (2001) Composição específica e abundância de peixes de zonas rasas dos cinco estuários do Rio Grande do Sul, Brasil. Boletim do Instituto de Pesca, São Paulo 27, 109–121.Google Scholar
Reis, E.G. (1986a) Age and growth of the marine catfish, Netuma barba (Siluriformes, Ariidae), in the estuary of the Patos Lagoon (Brazil). Fishery Bulletin 84, 679–686.Google Scholar
Reis, E.G. (1986b) Reproduction and feeding habits of the marine catfish, Netuma barba (Siluriformes, Ariidae), in the estuary of the Patos Lagoon (Brazil). Atlântica 8, 35–55.Google Scholar
Rosa-Filho, J.S. and Bemvenuti, C.E. (1998) Caracterización de las comunidades macrobentónicas de fondos blandos en regiones estuarinas de Rio Grande do Sul (Brasil). Thalassas 14, 43–56.Google Scholar
Rudershausen, P.J., Tuomikoski, J.A. and Buckel, J.A. (2005) Prey selectivity and diet of striped bass in Western Albemarle Sound, North Carolina. Transactions of the American Fisheries Society 134, 1059–1074.CrossRefGoogle Scholar
Sardiña, P. and Lopez, A.C. (2005) Feeding interrelationships and comparative morphology of two young sciaenids co-occurring in south-western Atlantic waters. Hydrobiologia 548, 41–49.CrossRefGoogle Scholar
Sazima, I. (1983) Scale-eating characoids and other fishes. Environmental Biology of Fishes 9, 87–101.CrossRefGoogle Scholar
Sazima, I. and Uieda, V.S. (1980) Comportamento lepidofágico de Oligoplites saurus e registro de lepidofagia em O. palometa e O. saliens (PISCES: CARANGIDAE). Revista Brasileira de Biologia 40, 701–710.Google Scholar
Scharf, F.S., Juanes, F. and Sutherland, M. (1998) Inferring ecological relationships from the edges of scatter diagrams: comparison of regression techniques. Ecology 79, 448–460.CrossRefGoogle Scholar
Scharf, F.S., Juanes, F. and Rountree, R.A. (2000) Predator size–prey size relationships of marine fish predators: interspecific variation and effects of ontogeny and body size on trophic-niche breadth. Marine Ecology Progress Series 208, 229–248.CrossRefGoogle Scholar
Scharf, F.S., Manderson, J.P., Fabrizio, M.C., Pessutti, J.P., Rosendale, J.E., Chant, R.J. and Bejda, A.J. (2004) Seasonal and interannual patterns of distribution and diet of bluefish within a middle Atlantic bight estuary in relation to abiotic and biotic factors. Estuaries 27, 426–436.CrossRefGoogle Scholar
Schoener, T.W. (1974) Resources partitioning in ecological communities. Science 185, 27–39.CrossRefGoogle ScholarPubMed
Schwarzbold, A. and Schäfer, A. 1984. Gênese das lagoas costeiras do Rio Grande do Sul—Brasil. Amazoniana 9, 87–104.Google Scholar
Seeliger, U. (2001) The Patos Lagoon estuary, Brazil. In Seeliger, U. and Kjerfve, V. (eds) Coastal marine ecosystems of Latin America. Berlin: Springer-Verlag, pp. 167–184.CrossRefGoogle Scholar
Sokal, R.R. and Rohlf, F.J. (1981) Biometry. 2nd edition. New York: Freeman.Google Scholar
Stehlik, L.L. and Meise, C.J. (2000) Diet of winter flounder in a New Jersey estuary: ontogenetic change and spatial variation. Estuaries 23, 381–391.CrossRefGoogle Scholar
Szedlmayer, S.D. and Lee, J.D. (2004) Diet shifts of juvenile red snapper (Lutjanus campechanus) with changes in habitat and fish size. Fishery Bulletin 102, 366–375.Google Scholar
Velasco, G., Reis, E.G. and Vieira, J.P. (2007) Calculating growth parameters of Genidens barbus (Siluriformes, Ariidae) using length composition and age data. Journal of Applied Ichthyology 23, 64–69.CrossRefGoogle Scholar
Vieira, J.P. (2006) Ecological analogies between estuarine bottom trawl fish assemblages from Patos Lagoon (32S), Brazil, and York River (37N), USA. Revista Brasileira de Zoologia 23, 234–247.CrossRefGoogle Scholar
Vieira, J.P., Castello, J.P. and Pereira, L.E. (1998) Ictiofauna. In Seeliger, U., Odebrecht, C. and Castello, J.P. (eds) Os ecossistemas costeiro e marinho do extremo sul de Brasil. Brasil: Editora Ecoscientia, pp. 60–68.Google Scholar
Wallace, R.K. (1981) An assessment of diet-overlap indexes. Transactions of the American Fisheries Society 110, 72–76.2.0.CO;2>CrossRefGoogle Scholar
Werner, E.E. and Guilliam, J.F. (1984) The ontogenetic niche and species interactions in size-structured populations. Annual Review of Ecology and Systematics 15, 393–426.CrossRefGoogle Scholar
Wheeler, A.P. and Allen, M.A. (2003) Habitat and diet partitioning between shoal bass and largemouth bass in the Chipola River, Florida. Transactions of the American Fisheries Society 132, 438–449.2.0.CO;2>CrossRefGoogle Scholar
Zahorcsak, P., Silvano, R.A.M. and Sazima, I. (2000) Feeding biology of a guild of benthivorous fishes in a sandy shore on south-eastern Brazilian coast. Revista Brasileira de Biologia 60, 511–518.CrossRefGoogle Scholar
Zar, J.H. (1984) Biostatistical analysis. 2nd edition. Upper Saddle River, NJ: Prentice Hall Inc.Google Scholar