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Evidence for selective mortality in Chlamys varia (L.) transplant experiments

Published online by Cambridge University Press:  11 May 2009

E. M. Gosling  and
G. M. Burnell
E. M. Gosling
Affiliation:
Regional Technical College and Zoology Department, University College, Galway, Ireland
G. M. Burnell
Affiliation:
Zoology Department, University College, Cork, Ireland
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Abstract

Two hundred Chlamys varia (L.) from Roskeeda Bay (W. Ireland) and Lough Hyne (S. Ireland) were collected and labelled in December 1979. One hundred individuals from the L. Hyne sample were then transferred to Roskeeda; similarly, 100 Roskeeda scallops were transferred to L. Hyne. At each site 100 indigenous scallops were held as controls.

After a period of approximately 1 year, survivors at each site were scored at 13 enzyme/protein loci using starch gel electrophoresis. Significant genetic differences were observed at the Pgm and Lap loci between native L. Hyne and native Roskeeda scallops. These differences persisted between surviving Roskeeda scallops (92% of the original sample) transferred to L. Hyne. However, after one year L. Hyne scallops transferred to Roskeeda (61% of original sample) did not differ significantly from indigenous Roskeeda scallops. Possible reasons for the observed selective mortality at this site are discussed.

Type
Research Article
Information
Journal of the Marine Biological Association of the United Kingdom , Volume 68 , Issue 2 , May 1988 , pp. 251 - 258
Copyright
Copyright © Marine Biological Association of the United Kingdom 1988

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References

Ayala, F. J., Powell, J. R., Tracy, M. L., Mourao, C. L. & Perez-Salas, S., 1972. Enzyme variability in the Drosophila willistoni group. IV. Genetic variation in natural populations of Drosophila willistoni. Genetics, 70, 113–139.CrossRefGoogle ScholarPubMed
Beaumont, A. R. & Beveridge, C. M., 1984. Electrophoretic survey of genetic variation in Pecten maximus, Chlamys opercularis, C. varia and C. distorta from the Irish Sea. Marine Biology, 81, 299–306.CrossRefGoogle Scholar
Burnell, G. M., 1983. Growth and Reproduction of the Scallop Chlamys varia (L.)on the West Coast of Ireland. Ph.D. Thesis, National University of Ireland, Dublin, Ireland.Google Scholar
Diehl, W. J. & Koehn, R. K., 1985. Multiple-locus heterozygosity, mortality and growth in a cohort of Mytilus edulis. Marine Biology, 88, 265–271.CrossRefGoogle Scholar
Gosling, E. M., 1982. Genetic variability in hatchery-produced Pacific oysters (Crassostrea gigas Thunberg). Aquaculture, 26, 273–287.CrossRefGoogle Scholar
Johnson, A. G. & Utter, F. M., 1973. Electrophoretic variants of aspartate aminotransferase of the bay mussel, Mytilus edulis (Linnaeus, 1758). Comparative Biochemistry and Physiology, 44B, 317–323.Google Scholar
Kitching, J. A., Ebling, F. J., Gamble, J. C., Hoare, R., McLeod, A. A. Q. R. & Norton, T. A., 1976. The ecology of Lough Hyne. XIX. Seasonal changes in the western trough. Journal of Animal Ecology, 45, 731–758.CrossRefGoogle Scholar
Koehn, R. K., 1984. The Application of Genetics to Problems in the Marine Environment: Future Areas of Research. Swindon: Natural Environment Research Council.Google Scholar
Koehn, R. K., Milkman, R. & Mitton, J. B., 1976. Population genetics of marine pelecypods. IV. Selection, migration and genetic differentiation in the blue mussel Mytilus edulis. Evolution, 30, 2–32.CrossRefGoogle ScholarPubMed
Mathers, N. F., 1975. Environmental variability at the phosphoglucose isomerase locus in the genus Chlamys. Biochemical Systematics and Ecology, 3, 123–127.CrossRefGoogle Scholar
Minchin, D., 1984. Aspects of the Biology of Young Escallops Pecten maximus. L. (Pectinidae: Bivalvia) about the Irish Coast. Ph.D. Thesis, Trinity College, University of Dublin, Ireland.Google Scholar
Murdock, E. A., Furguson, A. & Seed, R., 1975. Geographical variation in leucine aminopeptidase in Mytilus edulis L. from the Irish coasts. Journal of Experimental Marine Biology and Ecology, 19, 33–41.CrossRefGoogle Scholar
Raine, R. T. C. & Patching, J. W., 1979. Seasonal cycles of decomposition and production of organic material by the benthos of a semi-enclosed bay. In Cyclic Phenomena in Marine Plants and Animals. Proceedings of the 13th European Marine Biology Symposium, Isle of Man, 1978 (ed. Naylor, E. and Hartnoll, R. G.), pp. 241–248. Oxford: Pergamon Press.CrossRefGoogle Scholar
Rodhouse, P. G. & Burnell, G. M., 1979. In situ studies on the scallop Chlamys varia. Progress in Underwater Science, 4, 87–97.Google Scholar
Scopes, R. K., 1968. Method for starch gel electrophoresis of sarcoplasmic proteins. An investigation of the relative mobilities of the glycolytic enzymes from the muscles of a variety of species. Biochemical Journal, 107, 139–150.CrossRefGoogle ScholarPubMed
Smith, P. J. & Francis, R. I. C. C., 1983. Relationship between esterase gene frequencies and length in juvenile snapper Chryophrys auratus Forster. Animal Blood Groups and Biochemical Genetics, 14, 151–158.CrossRefGoogle Scholar
Sokal, R. R. & Rohlf, F. J., 1981. Biometry. San Francisco: W. H. Freeman & Co.Google Scholar
Theisen, B. F., 1978. Allozyme clines and evidence of strong selection in three loci in Mytilus edulis L. (Bivalvia) from Danish waters. Ophelia, 17, 135–142.CrossRefGoogle Scholar
Vahl, O., 1980. Seasonal variations in seston and in the growth rate of the Iceland scallop, Chlamys islandica (O. F. Müller) from Balsfjord, 70° N. Journal of Experimental Marine Biology and Ecology, 48, 195–204.CrossRefGoogle Scholar
Wilkins, N. P., 1978. Length-correlated changes in heterozygosity at an enzyme locus in the scallop (Pecten maximus L.). Animal Blood Groups and Biochemical Genetics, 9, 69–77.CrossRefGoogle Scholar