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Marine and Freshwater Research Marine and Freshwater Research Society
Advances in the aquatic sciences
RESEARCH ARTICLE

Assessing the trophic link between seagrass habitats and piscivorous fishes

Jeremy S. Hindell
+ Author Affiliations
- Author Affiliations

A Department of Zoology, University of Melbourne, VIC 3010, Australia.

B Marine and Freshwater Systems, PO Box 114, Queenscliff, VIC 3225, Australia. Email: jeremy.hindell@dpi.vic.gov.au

Marine and Freshwater Research 57(1) 121-131 https://doi.org/10.1071/MF05082
Submitted: 5 May 2005  Accepted: 8 November 2005   Published: 17 January 2006

Abstract

Links between piscivorous fishes and seagrass habitat were investigated in Port Phillip Bay, Australia. Abundances of piscivorous fish were estimated, the contribution of fish to their diets was measured and the trophic link between these fish and seagrass beds was assessed with stable isotopes. Piscivorous fishes were common in seagrass and included eight species from seven families (33% by abundance). They consumed at least eight families of teleost prey, including juveniles of seagrass-associated taxa, such as monacanthids (e.g. Meuschenia freycineti) and syngnathids (Stigmatopora argus). No fish were exclusively piscivorous and contribution of fish to the diets of the most common species (Arripis truttacea and Kestratherina esox) varied strongly through time. Putative contributions of each source (primary producer – plant) to the nutrition of piscivorous fishes were: (1) fishes whose base for nutritional support was driven mostly (>50%) by seagrass (e.g. Platycephalus speculator and Platycephalus laevigatus); and (2) fishes whose base for nutritional support was not driven by any particular primary producer (e.g. Arripis truttacea and Pseudocaranx dentex). The propensity for piscivorous fish to include seagrass-associated fish in their diets, their perennial presence in seagrass and the strong putative contribution by seagrass to their nutrition, suggest that seagrass habitats can be valuable habitat for piscivorous fishes.

Extra keywords: carbon, diet analysis, habitat links, nitrogen, piscivory, prey, stable isotope.


Acknowledgments

Earlier versions of this manuscript were improved by comments from A. Longmore, E. Morris, R. Connolly and anonymous reviewers. Thanks also to M. Hendricks, L. McGrath, M. Wheatley and R. Watson for assistance in the field and at the research station. I gratefully acknowledge funding from the Fisheries Research and Development Corporation (1999/215) and the University of Melbourne. Research was done using the facilities at the Queenscliff Marine Station. This research complies with current laws in Australia.


References

Beaudoin, C. P. , Tonn, W. M. , Prepas, E. E. , and Wassenaar, L. I. (1999). Individual specialization and trophic adaptability of northern pike (Esox lucius): an isotope and dietary analysis. Oecologia 120, 386–396.
Crossref | GoogleScholarGoogle Scholar | Bell J. D., and Pollard D. A. (1989). Ecology of fish assemblages and fisheries associated with seagrasses. In ‘Biology of Seagrasses: A Treatise on the Biology of Seagrasses with Special Reference to the Australian Region’. (Eds A. W. D. Larkum, A. J. McComb and S. Shepherd.) pp. 565–609. (Elsevier: Amsterdam.)

Bouillon, S. , Raman, A. , Dauby, P. , and Dehairs, F. (2002). Carbon and nitrogen stable isotope ratios of subtidal benthic invertebrates in an estuarine mangrove ecosystem (Andhra Pradesh, India). Estuarine, Coastal and Shelf Science 54, 901–913.
Crossref | GoogleScholarGoogle Scholar | Connolly R., Jenkins G., and Loneragan N. (1999). Seagrass dynamics and fisheries sustainability. In ‘Seagrass in Australia: Strategic Review and Development of an R&D Plan’. (Eds A. Butler and P. Jernakoff.) pp. 25–64. (CSIRO Marine Research: Melbourne.)

Currin, C. A. , Newell, S. Y. , and Paerl, H. W. (1995). The role of standing dead Spartina alterniflora and benthic microalgae in salt marsh food webs – considerations based on multiple stable isotope analysis. Marine Ecology Progress Series 121, 99–116.
Howard R. K., Edgar G. J., and Hutchings P. A. (1989). Faunal assemblages of seagrass beds. In ‘Biology of Seagrasses’. (Eds A. W. D. Larkum, A. J. McComb and S. A. Shepherd.) pp. 536–564. (Elsevier: Amsterdam.)

Hutchings, P. (1981). The fauna of Australian Seagrass Beds. Proceedings of the Linnean Society of NSW 106, 181–200.
Jenkins G. P., Edgar G. J., May H. M. A., and Shaw C. (1993). Ecological basis for parallel declines in seagrass habitat and catches of commercial fish in Western Port Bay, Victoria. In ‘Sustainable Fisheries Through Sustaining Fish Habitat. Australian Society for Fish Biology Workshop, Victor Harbour, SA, 12–13 August, Bureau of Resource Sciences Proceedings’. (Ed. D. A. Hancock.) pp. 124–136. (AGPS: Canberra.)

Jenkins, G. P. , Watson, G. F. , Hammond, L. S. , Black, K. P. , Wheatley, M. J. , and Shaw, C. (1996). Importance of shallow water, reef-algal habitats as nursery areas for commercial fish from southeastern Australia. Marine and Freshwater Resources Institute Fisheries Research and Development Corporation 92(44),
Keough M. J., and Jenkins G. P. (1995). Seagrass meadows and their inhabitants. In ‘Coastal Marine Ecology of Temperate Australia’. (Eds A. J. Underwood and M. G. Chapman.) pp. 341. (University of NSW Press: Sydney.)

Klumpp, D. W. , and Nichols, P. D. (1983). Utilisation of the seagrass Posidonia australis as food by the rock crab Nectocarcinus integrifrons (Latreille) (Crustacea: Decapoda: Portunidae). Marine Biology Letters 4, 331–339.
Klumpp D. W., Howard R. K., and Pollard D. A. (1989). Trophodynamics and nutritional ecology of seagrass communities. In ‘Biology of Seagrasses’. (Eds A. W. D. Larkum, A. J. McComb and S. A. Shepherd.) pp. 394–457. (Elsevier: Amsterdam.)

Loneragan, N. R. , Bunn, S. E. , and Kellaway, D. M. (1997). Are mangroves and seagrasses sources of organic carbon for penaeid prawns in a tropical Australian estuary? A multiple stable-isotope study. Marine Biology 130, 289–300.
Crossref | GoogleScholarGoogle Scholar | Longmore A., Nicholson G., and Abbott B. (2003). Identifying habitats important to the food supply of commercial fish in Western Port. Marine and Freshwater Resources Institute Report 36.

Melville, A. J. , and Connolly, R. M. (2003). Spatial analysis of stable isotope data to determine primary sources of nutrition for fish. Oecologia 136, 499–507.
Crossref | GoogleScholarGoogle Scholar | PubMed | Orth R. J. (1992). A perspective on plant-animal interactions in seagrasses: physical and biological determinants influencing plant and animal abundance. In ‘Plant–Animal Interactions in the Marine Benthos’. (Eds D. M. John, S. J. Hawkins and J. H. Price.) pp. 147–164. (Clarendon Press: Oxford.)

OzEstuaries (2005). Estuary Assessment 2000. National Land & Water Resources Audit: A program of the Natural Heritage Trust. Available online at: http://www.ozestuaries.org/ (verified December 2005).

Peterson, B. J. , and Fry, B. (1987). Stable isotopes in ecosystem studies. Annual Review of Ecology and Systematics 18, 293–320.
Crossref | GoogleScholarGoogle Scholar | Quinn G., and Keough M. (2002). ‘Experimental Design and Data Analysis for Biologists.’ (Cambridge University Press: Cambridge.)

Sheaves, M. (2001). Are there really few piscivorous fishes in shallow estuarine habitats? Marine Ecology Progress Series 222, 279–290.


Sydeman, W. J. , Hobson, K. A. , Pyle, P. , and McLaren, E. B. (1997). Trophic relationships among seabirds in central California: combined stable isotope and conventional dietary approach. The Condor 99, 327–336.


Thresher, R. E. , Nichols, P. D. , Gunn, J. S. , Bruce, B. D. , and Furlani, D. M. (1992). Seagrass detritus as the basis of a coastal planktonic food chain. Limnology and Oceanography 37, 1754–1758.


Vizzini, S. , Sara, G. , Michener, R. , and Mazzola, A. (2002). The role and contribution of the seagrass Posidonia oceanica (L.) Delile organic matter for secondary consumers as revealed by carbon and nitrogen stable isotope analysis. Acta Oecologica 23, 277–285.
Crossref | GoogleScholarGoogle Scholar |