Hostname: page-component-8448b6f56d-42gr6 Total loading time: 0 Render date: 2024-04-25T05:58:14.281Z Has data issue: false hasContentIssue false

Distribution, abundance, population structure and activity of Halobatrachus didactylus in the Tagus estuary (Portugal) and adjacent coastal waters

Published online by Cambridge University Press:  01 November 2011

João Carlos Cotter
Affiliation:
Center of Oceanography, Faculty of Sciences, University of Lisbon, Lisbon, Portugal
Tadeu José Pereira*
Affiliation:
Center of Oceanography, Faculty of Sciences, University of Lisbon, Lisbon, Portugal
Maria José Costa
Affiliation:
Center of Oceanography, Faculty of Sciences, University of Lisbon, Lisbon, Portugal Department of Animal Biology, Faculty of Sciences, University of Lisbon, Lisbon, Portugal
José Lino Costa
Affiliation:
Center of Oceanography, Faculty of Sciences, University of Lisbon, Lisbon, Portugal Department of Animal Biology, Faculty of Sciences, University of Lisbon, Lisbon, Portugal
*
Correspondence should be addressed to: T.J. Pereira, Center of Oceanography, Faculty of Sciences, University of Lisbon, Campo Grande, 1749-016 Lisbon, Portugal email: tjpereira@fc.ul.pt

Abstract

The Lusitanian toadfish Halobatrachus didactylus is a demersal teleost and the only species of the family Batrachoididae that occurs along the continental Portuguese coast. It is a subtropical species that is more abundant in the south of Portugal, whereas along the western coast it is concentrated in discrete populations, located in estuaries and coastal recesses. The distinct features of these estuaries have revealed important changes in the respective Lusitanian toadfish populations, namely particularities in their distribution and population structure, and also in the morphology and breeding behaviour of the specimens. A survey covering 31 stations in the Tagus estuary, Portugal, and adjacent coastal waters sampled these stations over an 18 month period. This study characterized the distribution, abundance, population structure and activity of H. didactylus in this coastal zone. Toadfish showed a preferential distribution in the intermediate and lower estuarine stretches, and was more abundant in the Montijo Bay, a small bay within the Tagus estuary. Three length-groups were identified, with larger specimens more abundant in deeper areas. The specimens also revealed a preference for areas of higher water temperature, low water current and muddy substrates. Female specimens were slightly more abundant than males and type II males had a very low frequency of occurrence (3.2%). Captures of toadfish were high in spring and late summer and very low in winter.

Type
Research Article
Copyright
Copyright © Marine Biological Association of the United Kingdom 2011

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

Amorim, M.C.P., Simões, J.M. and Fonseca, P.J. (2008) Acoustic communication in the Lusitanian toadfish, Halobatrachus didactylus: evidence for an unusual large vocal repertoire. Journal of the Marine Biological Association of the United Kingdom 88, 10691073.CrossRefGoogle Scholar
Amorim, M.C.P. and Vasconcelos, R.O. (2008) Variability in the mating calls of the Lusitanian toadfish Halobatrachus didactylus: potential cues for individual recognition. Journal of Fish Biology 73, 12771283.CrossRefGoogle Scholar
Archer, J. (1988) The behavioural biology of aggression. Cambridge, UK: Cambridge University Press.Google Scholar
Bauchot, M.-L. (1987) Poissons osseaux. In Fischer, W., Schneider, M. and Bauchot, M.-L. (eds) Fiches FAO d'identification des espèces pour les besoins de la pêche. Mediterranée et Mer Noire (Zone de Pêche 37). Revision 1. Volume II—Vertébrés. Rome: Organisation des Nations-Unies pour l'Alimentation et l'Agriculture, pp. 8911421.Google Scholar
Beja, P.R. (1995) Structure and seasonal fluctuations of rocky littoral fish assemblages in south-western Portugal: implications for otter prey availability. Journal of the Marine Biological Association of the United Kingdom 75, 833847.CrossRefGoogle Scholar
Bettencourt, A.M., Gomes, F.V., Dias, J.A., Ferreira, J.G., Silva, M.C. and Costa, J.L. (2003) Estuários portugueses. Lisbon: Instituto da Água.Google Scholar
Cabral, H. and Costa, M.J. (1999) Differential use of nursery areas within the Tagus estuary by sympatric soles, Solea solea and Solea senegalensis . Environmental Biology of Fishes 56, 389397.CrossRefGoogle Scholar
Cabral, H.N., Costa, M.J. and Salgado, J.P. (2001) Do the Tagus estuary fish community reflect environmental changes? Climate Research 18, 119126.CrossRefGoogle Scholar
Campos, M.C., Costa, J.L., Quintella, B.R. and Almeida, P.R. (2008) Activity and movement patterns of the Lusitanian toadfish inferred from pressure sensitive data-loggers in the Mira estuary (Portugal). Fisheries Management and Ecology 15, 449458.CrossRefGoogle Scholar
Cárdenas, S. (1977) Régimen alimenticio del sapo, Halobatrachus didactylus (Schneider, 1801) (Pisces: Batrachoididae), en la Bahía de Cádiz (España sudoccidental). Vie et Milieu Serie A—Biolgie Marine 28, 111129.Google Scholar
Costa, J.L. (2004) A biologia do xarroco Halobatrachus didactylus (Bloch & Schneider, 1801) e o seu papel na estrutura e funcionamento dos ecossistemas em que se insere; referência especial à população do estuário do Mira. PhD thesis. University of Lisbon, Portugal.Google Scholar
Costa, J.L., Almeida, P.R. and Costa, M.J. (2003) A morphometric and meristic investigation of Lusitanian toadfish Halobatrachus didactylus (Bloch & Schneider, 1801): evidence of population fragmentation on Portuguese coast. Scientia Marina 67, 219231.CrossRefGoogle Scholar
Costa, J.L. and Costa, M.J. (2002) Distribution and abundance of the Lusitanian toadfish, Halobatrachus didactylus (Bloch & Schneider, 1801) in Portugal with some remarks on its population fragmentation. Revista de Biologia 20, 155167.Google Scholar
Costa, J.L., Domingos, I., Almeida, A.J., Feunteun, E. and Costa, M.J. (2008) The interaction between Halobatrachus didactylus and Anguilla anguilla: what happens when these species occur in sympatry? Cybium 32, 111117.Google Scholar
Costa, J.L., Silva, G., Almeida, P.R. and Costa, M.J. (2000) Activity and diet of Halobatrachus didactylus (Bloch & Schneider, 1801) adults in the Tagus estuary. Thalassas 16, 2125.Google Scholar
Costa, M.J., Vasconcelos, R., Costa, J.L. and Cabral, H.N. (2007) River flow influence on the fish community of the Tagus estuary (Portugal). Hydrobiologia 587, 113123.CrossRefGoogle Scholar
Hair, J.F. Jr, Anderson, R.E., Tatham, R.L. and Black, W.C. (1998) Multivariate data analysis. 5th edition. Upper Saddle River, NJ: Prentice-Hall.Google Scholar
Henriques, M., Gonçalves, E.J. and Almada, V.C. (1999) The conservation of littoral fish communities: a case study at Arrábida coast (Portugal). In Almada, V.C., Oliveira, R.F. and Gonçalves, E.J. (eds) Behaviour and conservation of littoral fishes. Lisbon: Instituto Superior de Psicologia Aplicada, pp. 473519.Google Scholar
Modesto, T. and Canário, V.M. (2003) Morphometric changes and sex steroid levels during the annual reproductive cycle of the Lusitanian toadfish, Halobatrachus didactylus . General and Comparative Endocrinology 131, 220231.CrossRefGoogle ScholarPubMed
Nikolsky, G.V. (1963) The ecology of fishes. London: Academic Press.Google Scholar
Palazón-Fernández, J.L., Arias, A.M. and Sarasquete, C. (2001) Aspects of the reproductive biology of the toadfish, Halobatrachus didactylus (Schneider, 1801) (Pisces: Batrachoididae). Scientia Marina 65, 131138.CrossRefGoogle Scholar
Pereira, T.J., Silva, G., Costa, M.J. and Costa, J.L. (2011) Life strategies of Halobatrachus didactylus (Bloch and Schneider, 1801) in the Tagus estuary: comparison among different morphotypes. Estuarine, Coastal and Shelf Science 93, 328335.CrossRefGoogle Scholar
Robertson, D.R. (1998) Implications of body size for interspecific interactions and assemblage organization among coral-reef fishes. Australian Journal of Ecology 23, 252257.CrossRefGoogle Scholar
Roux, C. (1986) Batrachoididae. In Whitehead, P.J., Bauchot, M.-L., Hureau, J.-C., Nielsen, J. and Tortonese, E. (eds) Fishes of the north-eastern Atlantic and the Mediterranean. Volume III. Paris: United Nations Educational, Scientific and Cultural Organisation, pp. 13601361.Google Scholar
Siegel, S. and Castellan, N.J. Jr (1988) Nonparametric statistics for the behavioral sciences. 2nd edition. New York: McGraw-Hill.Google Scholar
Silva, G., Costa, J.L., Almeida, P.R. and Costa, M.J. (2006) Structure and dynamics of a benthic invertebrate community in an intertidal area of the Tagus estuary, western Portugal: a six year data series. Hydrobiologia 555, 115128.CrossRefGoogle Scholar
Sokal, R.R. and Rohlf, F.J. (1995) Biometry: the principles and practice of statistics in biological research. 3rd edition. New York: W.H. Freeman.Google Scholar
ter Braak, C.J. and Šmilauer, P. (2002) CANOCO reference manual and CanoDraw for Windows user's guide: software for Canonical Community Ordination (version 4.5). Ithaca, NY: Microcomputer Power.Google Scholar