Growth and reproductive biology of tarwhine Rhabdosargus sarba (Sparidae) in eastern Australia
Julian M. Hughes A B , John Stewart A , Benjamin W. Kendall A and Charles A. Gray AA New South Wales Department of Primary Industries, Cronulla Fisheries Research Centre of Excellence, PO Box 21, Cronulla, NSW 2230, Australia.
B Corresponding author. Email: Julian.Hughes@dpi.nsw.gov.au
Marine and Freshwater Research 59(12) 1111-1123 https://doi.org/10.1071/MF08102
Submitted: 31 March 2008 Accepted: 26 September 2008 Published: 19 December 2008
Abstract
The growth and reproductive biology of the commercially and recreationally important sparid fish, tarwhine (Rhabdosargus sarba), was examined from the coastal waters of New South Wales (NSW), south-eastern Australia. Previous research on this species in other parts of the world has yielded conflicting results concerning its growth and reproductive biology. Age estimates were made by counting opaque zones in otolith sections. The method was validated by marking the otoliths of captive fish with alizarin complexone, and also by marginal increment analyses using otoliths from wild-caught fish. Both sexes grew at a similar rate. Von Bertalanffy growth function parameters were: L∞ = 26.40 ± 0.40 cm fork length (FL), k = 0.39 ± 0.02 year–1 and to = –0.56 ± 0.09 years. The maximum estimated age was 16.5 years. Spawning occurred from May to August with a peak in July. Both sexes matured at a similar size (L50 = 19.44 ± 0.15 cm FL), which was larger than the current minimum legal length in NSW. Ovotestes were identified in adult tarwhine and were confirmed by histological analyses. Results of this study provided evidence that tarwhine are likely to be rudimentary hermaphrodites in eastern Australia and are more similar in growth rate, maximum size/age, and reproductive biology to tarwhine from Western Australia than those from other parts of the world.
Additional keywords: maturity, minimum legal length, rudimentary hermaphrodite, spawning seasonality.
Acknowledgements
We thank W. Robbins and two anonymous reviewers for comments which significantly improved the manuscript. We also thank S. Barbosa for carrying out the histological analyses. This study was funded by the NSW Recreational Fishing Trust, the NSW Department of Primary Industries and the Fisheries Research and Development Corporation (Project No. 2004/035). Fish were collected under Scientific Research Permit No. P01/0059(A) and maintained in captivity under Animal Care and Ethics Approval No. 02/08.
Besseau, L. , and Bruslé-Sicard, S. (1995). Plasticity of gonad development in hermaphroditic sparids – ovotestis ontogeny in a protandric species, Lithognathus mormyrus. Environmental Biology of Fishes 43, 255–267.
| Crossref | GoogleScholarGoogle Scholar |
García-Rodríguez, M. , Fernández, Á. M. , and Esteban, A. (2006). Characterisation, analysis and catch rates of the small-scale fisheries of the Alicante Gulf (SE Spain) over a 10 years time series. Fisheries Research 77, 226–238.
| Crossref | GoogleScholarGoogle Scholar |
Grandcourt, E. M. , Al Abdessalaam, T. Z. , Francis, F. , and Al Shamsi, A. T. (2004). Biology and stock assessment of the sparids, Acanthopagrus bifasciatus and Argyrops spinifer (Forsskål, 1775), in the Southern Arabian Gulf. Fisheries Research 69, 7–20.
| Crossref | GoogleScholarGoogle Scholar |
Gray, C. A. , and Kennelly, S. J. (2003). Catch characteristics of the commercial beach-seine fisheries in two Australian barrier estuaries. Fisheries Research 63, 405–422.
| Crossref | GoogleScholarGoogle Scholar |
Kingsford, M. J. , and Hughes, J. M. (2005). Patterns of growth, mortality, and size of the tropical damselfish Acanthochromis polyacanthus across the continental shelf of the Great Barrier Reef. Fishery Bulletin 103, 561–573.
Leu, M. Y. (1994). Natural spawning and larval rearing of silver bream, Rhabdosargus sarba (Forsskal), in captivity. Aquaculture 120, 115–120.
| Crossref | GoogleScholarGoogle Scholar |
Patnaik, S. (1973). Some aspects of the fishery and biology of the Chilka khuranti, Rhabdosargus sarba (Forskal). Journal of the Inland Fisheries Society of India 5, 102–114.
Smale, M. J. (1998). Distribution and reproduction of the reef fish Petrus rupestris (Pisces, Sparidae) off the coast of South Africa. South African Journal of Zoology 23, 272–287.
Whitfield, A. K. (1998). Biology and ecology of fishes in southern African estuaries. Ichthyological Monographs of the J. L. B. Smith Institute of Ichthyology 2, 1–223.
Willis, T. J. , Millar, R. B. , and Babcock, R. C. (2003). Protection of exploited fish in temperate regions: high density and biomass of snapper Pagrus auratus (Sparidae) in northern New Zealand marine reserves. Journal of Applied Ecology 40, 214–227.
Worthington, D. G. , Ferrell, D. J. , McNeill, S. E. , and Bell, J. D. (1992). Growth of four species of juvenile fish associated with the seagrass Zostera capricorni in Botany Bay, New South Wales. Australian Journal of Marine and Freshwater Research 43, 1189–1198.
| Crossref | GoogleScholarGoogle Scholar |
Yeung, W. S. B. , and Chan, S. T. H. (1987). The gonadal anatomy and sexual pattern of the protandrous sex-reversing fish, Rhabdosargus sarba (Teleostei, Sparidae). Journal of Zoology 212, 521–532.