Gene flow, colonisation and demographic history of the flat oyster Ostrea angasi
David A. Hurwood A C , Mike P. Heasman B and Peter B. Mather AA School of Natural Resource Sciences, Queensland University of Technology, Gardens Point, GPO Box 2434, Brisbane, Qld 4001, Australia.
B New South Wales Fisheries, Port Stephens Fisheries Centre, Private Bag 1, Nelson Bay, NSW 2315, Australia.
C Corresponding author. Email: d.hurwood@qut.edu.au
Marine and Freshwater Research 56(8) 1099-1106 https://doi.org/10.1071/MF04261
Submitted: 12 October 2004 Accepted: 7 September 2005 Published: 22 November 2005
Abstract
The Australian flat oyster Ostrea angasi is currently being assessed for its potential as a species for culture in New South Wales. It is considered important to determine the population genetic structure of wild stocks among estuaries before translocation of juveniles (spat) for growout in order to avoid possible deleterious effects of hybridisation of genetically divergent stocks (i.e. outbreeding depression). Five estuaries were sampled in southern New South Wales as well as another four from across the natural range of the species in Australia. Sequence analysis of a 594 base pair fragment of the mitochondrial cytochrome oxidase I gene was used to determine the degree of population structuring inferred from pairwise ΦST estimates and spatial analysis of molecular variance analysis. The analyses revealed that there is no significant genetic differentiation among the sampled New South Wales estuaries (P > 0.05) and all eastern samples represent a geographically homogeneous population. This essentially removes any potential constraints on broodstock sourcing and spat translocation within this region. Although levels of differentiation among all sites varied, little divergence was evident across the entire range of the sample. Furthermore, the study revealed extremely low levels of divergence between O. angasi and its northern hemisphere congener, O. edulis, raising the possibility that O. angasi may have only recently colonised Australian estuaries.
Extra keywords: aquaculture, cytochrome oxidase I, Ostrea edulis, outbreeding depression, population structure.
Acknowledgments
We thank Nick Savva (Springbay Seafoods P/L, Tasmania), Xiaoxu Li (South Australian Aquaculture Research and Development Institute), Steve Feletti (Batemans Bay), David Maidment (Narooma), John Smith (Bermagui), Chris and Dominic Boyton (Merimbula), Mike ‘Banjo’ Young (Pambula), Matthew Muggleton (Yorke Regional Development Board, South Australia) and Phil Button (OceanFoods International P/L, Western Australia) for the supply of oyster tissue samples. Assistance in the laboratory from Juanita Renwick, Vincent Chand and Tanya Walsh is gratefully acknowledged. The manuscript was greatly improved through the comments of four anonymous reviewers.
Barber, P. H. , Palumbi, S. R. , Erdmann, M. V. , and Moosa, M. K. (2002). Sharp genetic breaks among populations of Haptosquilla pulchella (Stomatopoda) indicates limits to larval transport: patterns, causes, and consequences. Molecular Ecology 11, 659–674.
| Crossref | GoogleScholarGoogle Scholar | PubMed |
Cross, T. F. (2000). Genetic implications of translocation and stocking of fish species, with particular reference to Western Australia. Aquaculture Research 31, 83–94.
| Crossref | GoogleScholarGoogle Scholar |
Hoskin, M. G. (2000). Effects of the East Australian Current on the genetic structure of a direct developing muricid snail (Bedeva hanleyi, Angas): variability within and among local populations. Biological Journal of the Linnean Society 69, 245–262.
| Crossref | GoogleScholarGoogle Scholar |
Slatkin, M. (1993). Isolation by distance in equilibrium and non-equilibrium populations. Evolution 47, 264–279.
Youngson, A. F. , Dosdat, A. , Saroglia, M. , and Jordan, W. C. (2001). Genetic interactions between marine finfish species in European aquaculture and wild conspecifics. Journal of Applied Ichthyology 17, 153–162.
| Crossref | GoogleScholarGoogle Scholar |