Skip to main content
Log in

Gametic incompatibility and genetic divergence of Pacific and Kumamoto oysters, Crassostrea gigas and C. sikamea

  • Published:
Marine Biology Aims and scope Submit manuscript

Abstract

The biological and taxonomic separation of the Pacific oyster Crassostrea gigas (Thunberg, 1793) from the Kumamoto oyster C. sikamea (Amemiya, 1928) is affirmed by three concordant lines of evidence: (1) fixed differences in 2% of a mtDNA sequence coding for large subunit rRNA; (2) a genetic distance of 0.440 based on 19 allozyme loci, including 5 diagnostic loci (Aat-1, Idh-1, Idh-2, Mpi-1, Mdh-2); (3) one-way gametic incompatibility resulting in partial reproductive isolation in interspecific crosses. C. gigas sperm x C. sikamea egg fertilizations form viable hybrid offspring, but C. sikamea sperm do not fertilize C. gigas eggs. Divergence between these two species is mediated by differing peaks in the periods for gamete release and by one-way sperm/egg incompatibility. Two attempts to recover C. sikamea from its place of origin in southern Japan have yielded only individuals with the mitochondrial haplotype that characterizes C. gigas. We thus identify a crucial need for careful screening, management, and conservation of the cultivated populations of C. sikamea on the US west coast.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Ahmed M (1975) Speciation in living oysters. Adv mar Biol 13:275–397

    Google Scholar 

  • Allen SK, Bushek D (1992) Large-scale production of triploid oysters, Crassostrea virginica (Gmelin), using “stripped” gametes. Aquaculture, Amsterdam 103:241–251

    Google Scholar 

  • Allen SK, Downing SL, Chew KK (1989) Hatchery manual for producing triploid oysters. University of Washington, Seattle, USA (Washington Sea Grant Program, Publ WSG 89-3)

    Google Scholar 

  • Amemiya I (1928) Ecological studies of Japanese oysters, with special reference to the salinity of their habitats. J Coll Agric imp Univ 9:333–382

    Google Scholar 

  • Ayala FJ, Powell JR (1972) Allozymes as diagnostic characters of sibling species of Drosophila. Proc natn Acad Sci USA 69:1094–1096

    Google Scholar 

  • Ayala FJ, Tracey ML, Hedgecock D, Richmond RC (1973) Genetic differentiation during the speciation process in Drosophila. Evolution 28:576–592

    Google Scholar 

  • Banks MA, Waters C, Hedgecock D (1993) Discrimination between closely related Pacific oyster species (Crassostrea) via mitochondrial DNA sequences coding for large subunit rRNA. Molec mar Biol Biotechnol 2:129–136

    Google Scholar 

  • Berg CJ (1969) Seasonal gonadal changes of adult oviparous oysters in Tomales Bay, California Veliger 12:27–36

    Google Scholar 

  • Breese WP, Malouf RE (1975) Hatchery manual for the Pacific oyster. Oregon State University Sea Grant Publ No. ORESU-5-002. Agricultural Experiment Station, Corvallis, Oregon, USA (Spec Rep #443)

    Google Scholar 

  • Buroker NE, Hershberger WK, Chew KK (1979 a) Population genetics of the family Ostreidae. I. Intraspecific studies of Crassostrea gigas and Saccostrea commercialis. Mar Biol 54:157–169

    Google Scholar 

  • Buroker NE, Hershberger WK, Chew KK (1979 b) Population genetics of the family Ostreidae. II. Interspecific studies of the genera Crassostrea and Saccostrea. Mar Biol 54:171–184

    Google Scholar 

  • Chew KK (1979) The Pacific oyster (Crassostrea gigas) in the west coast of the United States. In: Mann R (ed) Exotic species in mariculture. MIT Press, Cambridge, Massachusetts, USA, pp 54–82

    Google Scholar 

  • Foltz KR, Lennarz, WJ (1993) Review: The molecular basis of sea urchin gamete interactions at the egg plasma membrane. Devl Biol 158:46–61

    Google Scholar 

  • Grant V (1966) The selective origin of incompatibility barriers in the plant genus Gilia Am Nat 100:99–118

    Google Scholar 

  • Hedgecock D (1994) Does variance in reproductive success limit effective population sizes of marine organisms? In: Beaumont AR (ed) Genetics and evolution of aquatic organisms. Chapman & Hall, Lond, pp 122–134

    Google Scholar 

  • Hedgecock D, Banks MA, McGoldrick DJ (1993) The status of the Kumamoto oyster Crassostrea sikamea (Amemiya 1928) in U.S. commercial brood stocks. J Shellfish Res 12:215–221

    Google Scholar 

  • Hedgecock D, Cooper K, Hershberger W (1991) Genetic and environmental components of variance in harvest body size among pedigreed Pacific oysters Crassostrea gigas from controlled crosses. J Shellfish Res 10:p 516

    Google Scholar 

  • Hedgecock D, Sly F (1990) Genetic drift and effective population size of hatchery-propagated stocks of the Pacific oyster Crassostrea gigas. Aquaculture, Amsterdam 88:21–38

    Google Scholar 

  • Imai T, Sakai S (1961) Study of breeding the Japanese oyster, Crassostrea gigas. Tohoku J agric Res 12:125–171

    Google Scholar 

  • Lannan JE, Robinson A, Breese WP (1980) Broodstock management of Crassostrea gigas. II. Broodstock conditioning to maximize larval survival. Aquaculture, Amsterdam 21:337–345

    Google Scholar 

  • Leyton L, LeGuen P, Bunch D, Saling PM (1992) Regulation of mouse gamete interaction by sperm tyrosine kinase. Proc natn Acad Sci USA 89:11692–11695

    Google Scholar 

  • Majima R (1989) Cenozoic fossil naticidae (Mollusca: Gastropoda) in Japan. Bull Am Paleont 96:1–159

    Google Scholar 

  • Miller DJ, Macek MB, Shur BD (1992) Complementarity between sperm surface β-1,4-galactosyltransferase and egg-coat ZP3 mediates sperm-egg binding. Nature, Lond 357:589–593

    Google Scholar 

  • Nei M (1978) Estimation of average heterozygosity and genetic distance from a small number of individuals. Genetics, Austin, Tex 89:583–590

    Google Scholar 

  • Nei M (1987) Molecular evolutionary genetics. Academic Press. New York

    Google Scholar 

  • Numachi R (1978) Biological research on the oyster. In: Imai T (ed) Aquaculture in shallow seas. Balkema, Rotterdam, pp 115–204

    Google Scholar 

  • Ozaki H, Fujio Y (1985) Genetic differentiation in geographical populations of the Pacific oyster (Crassostrea gigas) around Japan. Tohoku J agric Res 36:49–61

    Google Scholar 

  • Palumbi SR (1992) Marine speciation on a small planet. Trends Ecol Evol 7:114–118

    Google Scholar 

  • Quayle DB (1988) Pacific oyster culture in British Columbia. Can Bull Fish aquat Sciences 218:1–241

    Google Scholar 

  • Robinson AM (1992) Gonadal cycle of Crassostrea gigas kumanoto (Thunberg) in Yaquina Bay, Oregon, and optimal conditions for broodstock conditioning and larval culture. Aquaculture, Amsterdam 106:89–97

    Google Scholar 

  • Saiki RK, Bugawan TL, Horn GT, Mullis KB, Erlich HA (1986) Analysis of enzymatically amplified-globin and HLA-DQa DNA with allele-specific oligonucleotide probes. Nature, Lond 324:163–166

    Google Scholar 

  • Stephano J, Gould M (1988) Avoiding polyspermy in the oyster (Crassostrea gigas). Aquaculture, Amsterdam. 73:295–307

    Google Scholar 

  • Woelke CE (1955) Introduction of the Kumamoto oyster Ostrea (Crassostrea) gigas to the Pacific coast. Fish Res Pap St Wash 1(3):41–50

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

Communicated by M. F. Strathmann, Friday Harbor

Rights and permissions

Reprints and permissions

About this article

Cite this article

Banks, M.A., McGoldrick, D.J., Borgeson, W. et al. Gametic incompatibility and genetic divergence of Pacific and Kumamoto oysters, Crassostrea gigas and C. sikamea . Marine Biology 121, 127–135 (1994). https://doi.org/10.1007/BF00349481

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00349481

Keywords

Navigation