Skip to main content
Log in

Allozyme variation in populations of the dog-whelkNucella lapillus (Prosobranchia: Muricacea) from the South West peninsula of England

  • Published:
Marine Biology Aims and scope Submit manuscript

Abstract

Four populations of the predatory gastropodNucella lapillus were sampled at sites around the South West Peninsula of England in 1986, and analysed for allozyme variation at 18 enzyme loci. Two of these loci, αGpd-1 andHk-1, exhibited sex-specific phenotypes. An absolute locus association was observed between two other loci,Mdh-1 andEst-3. This association was only found at one site (Prawle), and it is suggested that the presence of chromosomal polymorphisms could explain this finding. As a measure of overall similarity, Nei's genetic identity statistic,I, was calculated; the mean for all populations was 0.989, with values ranging from 0.981 to 0.997. Although similar on this gross level, considerable interpopulation variation was evident. Observed mean heterozygosity (per locus) ranged from 0.043 to 0.104 (mean 0.074). Populations differed also in the loci at which significant heterozygote deficits were seen (of the seven deficits recorded only those at thePep-1 locus were consistent across sites) and in the presence of rare alleles undetected elsewhere. The variation observed showed no correlation to shell morphology or geographical distance and confirmed the conclusion that species of the genusNucella show considerable disjunct variation.

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

Literature cited

  • Ahmad, M., Skibinski, D. O. F., Beardmore, J. A. (1977). An estimate of the amount of genetic variation in the common musselMytilus edulis. Biochem. Genet. 15: 833–846

    Google Scholar 

  • Avise, J. C. (1976). Genetic differentiation during speciation. In: Ayala, F. J. (ed.) Molecular evolution. Sinauer, Sunderland, Massachusetts, p. 106–122

    Google Scholar 

  • Ayala, F. J. (1975). Genetic differentiation during the speciation process. Evolutionary Biol. 8: 1–78

    Google Scholar 

  • Ballantine, W. J. (1961). A biologically-defined exposure scale for the comparative description of rocky shores. Fld Stud. 1: 1–19

    Google Scholar 

  • Bantock, C. R., Cockayne, W. C. (1976). Chromosomal polymorphism inNucella lapillus. Heredity, Lond. 34: 231–245

    Google Scholar 

  • Beaumont, A. R., Day, T. R., Gade, G. (1980). Genetic variation at the octopine dehydrogenase locus in the adductor muscle ofCerastoderma edule (L.) and six other bivalve species. Mar. Biol. Lett. 1: 137–148

    Google Scholar 

  • Berger, E. M. (1973). Gene-enzyme variation in three sympatric species ofLittorina. Biol. Bull. mar. biol. Lab., Woods Hole 145: 83–90

    Google Scholar 

  • Berger, E. M. (1977). Gene-enzyme variation in three sympatric species ofLittorina, II. The Roscoff population, with a note on the origin of North AmericanL. littorea. Biol. Bull. mar. biol. Lab., Woods Hole 153: 255–264

    Google Scholar 

  • Berry, R. J. (1983). Polymorphic shell-banding in the dog whelkNucella lapillus (Mollusca). J. Zool., Lond. 200: 455–470

    Google Scholar 

  • Berry, R. J., Crothers, J. H. (1968). Stabilizing selection in the dog whelk (Nucella lapillus). J. Zool., Lond. 155: 5–17

    Google Scholar 

  • Berry, R. J., Crothers, J. H. (1970). Genotypic stability and physiological tolerance in the dog-whelk (Nucella lapillus). J. Zool., Lond. 162: 293–302

    Google Scholar 

  • Berry, R. J., Crothers, J. H. (1974). Visible variation in the dog-whelk,Nucella lapillus. J. Zool., Lond. 174: 123–148

    Google Scholar 

  • Campbell, C. A. (1978). Genetic divergence between populations ofT. lamellosa (Gmelin). In: Battaglia, B., Beardmore, J. A. (eds.) Marine organisms: genetics, ecology and evolution. Plenum Press, New York, p. 157–170

    Google Scholar 

  • Crothers, J. H. (1983). Variation in dog whelk shells in relation to wave action and crab predation. Biol. J. Linn. Soc. 20: 85–102

    Google Scholar 

  • Fretter, V., Graham, A. (1962). British prosobranch molluscs. Their functional anatomy and ecology. Ray Society, London

    Google Scholar 

  • Gooch, J. L., Smith, B. S., Knupp, D. (1972). Regional survey of gene frequencies in the mud snail,Nassarius obsoletus. Biol. Bull. mar. biol. Lab., Woods Hole 142: 36–48

    Google Scholar 

  • Harris, H., Hopkinson, D. A. (1978). Handbook of enzyme electrophoresis in human genetics. North-Holland, Elsevier, Amsterdam

    Google Scholar 

  • Heller, J. (1975). The taxonomy of some BritishLittorina species with notes on their reproduction (Mollusca: Prosobranchia). Zool. J. Linn. Soc. 56: 131–151

    Google Scholar 

  • Hughes, R. N. (1972). Annual production of two Nova Scotian populations ofNucella lapillus (L.). Oecologia 8: 356–370

    Google Scholar 

  • Janson, K. (1983). Selection and migration in two distinct phenotypes ofLittorina saxatilis in Sweden. Oecologia 59: 58–61

    Google Scholar 

  • Janson, K. (1985). Genetic and morphological variation within and between populations ofLittorina angulifera from Florida. Ophelia 24: 125–134

    Google Scholar 

  • Janson, K., Ward, R. D. (1984). Microgeographic variation in allozyme and shell characters inLittorina saxatilis Olivi. (Prosobranchia: Littorinidae). Biol. J. Linn. Soc. 22: 289–307

    Google Scholar 

  • Kincaid, T. (1957). Local races and clines in the marine gastropod,Thais lamellosa Gmelin. A population study. Calliostoma Press, Seattle, Washington

    Google Scholar 

  • Kitching, J. A. (1976). Distribution and changes in shell form ofThais spp. (Gastropoda) near Bamfield, B.C. J. exp. mar. Biol. Ecol. 23: 109–126

    Google Scholar 

  • Kool, S. P. (1986). Systematic revision of thaidid genera based on anatomy. Bull. Am. malac. Un. 4: p. 110

    Google Scholar 

  • Lewontin, R. C. (1974). The genetic basis of evolutionary change. Columbia University Press, New York

    Google Scholar 

  • Mastro, E., Chow, V., Hedgecock, D. (1982).Littorina scrutalata, Littorina plena. Sibling species status of two prosobranch gastropod species confirmed by electrophoresis. Veliger 24: 239–246

    Google Scholar 

  • Morris, S. (1979). Genetic variation in the genusLittorina. Ph.D. dissertation. University of Wales

  • Nei, M. (1972). Genetic distance between populations. Am Nat. 106: 282–292

    Google Scholar 

  • Page, C. (1985). Investigation of the cytogenetics of marine and terrestrial gastropods. Ph. D. disseration. Polytechnic of North London

  • Palmer, A. R. (1984). Species cohesiveness and genetic control of shell colour and form inThais emarginata (Prosobranchia, Muricacea): preliminary results. Malacologia 25: 477–491

    Google Scholar 

  • Palmer, A. R. (1985). Genetic basis of shell variation inThais emarginata (Prosobranchia, Muricacea). 1. Banding in populations from Vancouver Island. Biol. Bull. mar. biol. Lab., Woods Hole 169: 638–651

    Google Scholar 

  • Pamilo, P., Varvio-Aho, S., (1984). Testing genotype frequencies and heterozygosities. Mar. Biol. 79: 99–100

    Google Scholar 

  • Schaal, B. A., Anderson, W. W. (1974). An outline of techniques for starch gel electrophoresis of enzymes from the American oysterCrassostrea virginica Gmelin. Tech. Rep. Ser. Ga mar. Sci. Cent. Savannah, Ga 74: 1–17

    Google Scholar 

  • Scheffe, H. (1959). The analysis of variance. John Wiley, New York

    Google Scholar 

  • Shaw, C. R., Prasad, R. (1970). Starch gel electrophoresis of enzymes — a compilation of recipes. Biochem. Genet 4: 297–320

    Google Scholar 

  • Snyder, T. P., Gooch, J. L. (1973). Genetic differentiation inLittorina saxatilis (Gastropoda). Mar. Biol. 22: 177–182

    Google Scholar 

  • Spight, T. M. (1973). Ontogeny, environment and shape of a marine snail,Thais lamellosa Gmelin. J. exp. mar. Biol. Ecol. 13: 215–228

    Google Scholar 

  • Staiger, H. (1957). Genetical and morphological variation inPurpura lapillus with respect to local and regional differentiation of population groups. Année biol. 33: 251–258

    Google Scholar 

  • Stern, E. M. (1975). The chromosomes ofViviparus subpurpureus (Say) (Streptoneura, Viviparidae). Malac. Rev. 13: 107–108

    Google Scholar 

  • Struhsaker, J. W. (1967). Selection mechanisms associated with intraspecific shell variation inLittorina picta. Evolution 22: 459–480

    Google Scholar 

  • Ward, R. D., Warwick, T. (1980). Genetic differentiation in the molluscan speciesLittorina rudis andLittorina arcana (Prosobranchia, Littorinidae). Biol. J. Linn. Soc. 14: 417–428

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

Communicated by J. Mauchline, Oban

Rights and permissions

Reprints and permissions

About this article

Cite this article

Day, A.J., Bayne, B.L. Allozyme variation in populations of the dog-whelkNucella lapillus (Prosobranchia: Muricacea) from the South West peninsula of England. Mar. Biol. 99, 93–100 (1988). https://doi.org/10.1007/BF00644981

Download citation

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00644981

Keywords

Navigation