Skip to main content
Log in

Genetic population structure of the southern oyster drillStramonita (=Thais)haemostoma

  • Published:
Marine Biology Aims and scope Submit manuscript

Abstract

Nine collections in the southeastern USA of the thaidid molluscStramonita haemastoma, comprising 963 individuals, were made between June 1988 and November 1989, and examined for allozyme variation at 18 electrophoretically-detected loci. Two genetically-differentiated groups were identified and are referred to ascanaliculata-like andfloridana-like snails, based on previously-described subspecies ofS. haemastoma. The two groups were differentiated genetically at a level that is characteristic of congeneric species in other molluscan taxa. The two groups maintained their genetic differences in areas of sympatry, although rare hybrid individuals occurred (about 1.2% of the total set). Shell and radular characters showed little variation within or between the two groups. Within each group, allozyme allele frequencies showed little geographic variation across distances as great as 1 500 km. This result is consistent with the suggestion that species with planktonic larvae (such asS. haemastoma) should have higher rates of gene flow than related brooding species.

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.

Institutional subscriptions

Similar content being viewed by others

Literature cited

  • Abbott, R. T. (1974). American seashells; the marine Mollusca of the Atlantic and Pacific coasts of North America. Van Nostrand Reinhold Co., New York

    Google Scholar 

  • Andrews, J. (1977). Shells and shores of Texas. University of Texas Press, Austin

    Google Scholar 

  • Bandel, K. (1984). The radulae of Caribbean and other Mesogastropoda and Neogastropoda. Zool. Verh., Leiden 214: 1–188

    Google Scholar 

  • Barton, N. H., Hewitt, G. M. (1983). Hybrid zones as barriers to gene flow. In: Oxford, G. S., Rollinson, D. (eds.) Protein polymorphism: adaptive and taxonomic significance. Academic Press, London, p. 341–359

    Google Scholar 

  • Bert, T. M. (1986). Speciation in western Atlantic stone crabs (genusMenippe): the role of geological processes and climatic events in the formation and distribution of species. Mar. Biol. 93: 157–170

    Article  Google Scholar 

  • Butler, P. A. (1954). The southern oyster drill. Proc. natn. Shellfish. Ass. 44: 67–75

    Google Scholar 

  • Burton, R. S. (1983). Protein polymorphisms and genetic differentiation of marine invertebrate populations. Mar. Biol. Lett. 4: 193–206

    Google Scholar 

  • Chambers, S. M. (1978). An electrophoretically detected sibling species of “Goniobasis floridensis” (Mesogastropoda: Pleuroceridae). Malacologia 17: 157–162

    Google Scholar 

  • Clench, W. J. (1947). The generaPurpura andThais in the western Atlantic. Johnsonia 2: 61–91

    Google Scholar 

  • Crisp, D. J. (1978). Genetic consequences of different reproductive strategies in marine invertebrates. In: Battaglia, B., Beardmore, J. A. (eds.) Marine organisms: genetics, ecology, and evolution. Plenum Press, New York, p. 257–273

    Google Scholar 

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

    Article  Google Scholar 

  • Grant, W. S., Utter, F. M. (1988). Genetic heterogeneity on different geographic scales inNucella lamellosa (Prosobranchia, Thaididae). Malacologia 28: 275–287

    Google Scholar 

  • Gunter, G. (1979). Studies of the southern oyster borer,Thais haemastoma. Gulf Res. Rep. 6: 249–260

    Google Scholar 

  • Hedgecock, D. (1986). Is gene flow from pelagic larval dispersal important in the adaptation and evolution of marine invertebrates? Bull. mar. Sci. 39: 550–564

    Google Scholar 

  • Hickman, C. S. (1980). Gastropod radula and the assessment of form in evolutionary paleontology. Paleobiology 6: 276–294

    Google Scholar 

  • Highsmith, R. C. (1985). Floating and algal rafting as potential dispersal mechanisms in brooding invertebrates. Mar. Ecol. Prog. Ser. 25: 169–179

    Google Scholar 

  • Janson, K. (1987). Allozyme and shell variation in two marine snails (Littorina, Prosobranchia) with different dispersal abilities. Biol. J. Linn. Soc. 30: 245–256

    Google Scholar 

  • Johannesson, K. (1988). The paradox of Rockall: why is a brooding gastropod (Littorina saxatilis) more widespread than one having a planktonic larval dispersal stage (L. littorea)? Mar. Biol. 99: 507–513

    Article  Google Scholar 

  • Johnson, C. W. (1934). List of the marine molluscs of the Atlantic coast from Labrador to Texas. Proc. Boston Soc. nat. Hist. 40: p. 118

    Google Scholar 

  • Jokiel, P. L. (1990). Long-distance dispersal by rafting: reemergence of an old hypothesis. Endeavour (New Ser.) 14: 66–73

    Article  Google Scholar 

  • Kool, S. P. (1987). Significance of radular characters in reconstruction of thaidid phylogeny (Neogastropoda: Muricacea). Nautilus 101: 117–132

    Article  Google Scholar 

  • Kool, S. P. (1989). Phylogenetic analysis of the subfamily Thaidinae (Prosobranchia: Neogastropoda: Muricidae). Ph. D. dissertation. George Washington University, Washington, DC

    Google Scholar 

  • Kwast, K. E., Foltz, D. W., Stickle, W. B. (1990). Population genetics and systematics of theLeptasterias hexactis (Echinodermata: Asteroidea) species complex. Mar. Biol. 105: 477–489

    Article  Google Scholar 

  • Liu, L. L. (1990). Genotypic and phenotypic variations of the southern oyster drills,Stramonita canaliculata andS. haemastoma floridana to salinity. Ph.D. dissertation. Louisiana State University, Baton Rouge

    Google Scholar 

  • Manwell, C., Baker, C. M. A. (1963). A sibling species of sea-cucumber discovered by starch gel electrophoresis. Comp. Biochem. Physiol. 10: 39–53

    Article  PubMed  Google Scholar 

  • McDonald, J. H., Koehn, R. K. (1988). The musselsMytilus galloprovincialis andM. trossulus on the Pacific coast of North America. Mar. Biol. 99: 111–118

    Article  Google Scholar 

  • Munksgaard, C. (1990). Electrophoretic separation of morphologically similar species of the genusRissoa (Gastropoda: Prosobranchia). Ophelia 31: 97–104

    Google Scholar 

  • Murphy, P. G. (1978).Collisella austrodigitalis sp. nov.: a sibling species of limpet (Acmaeidae) discovered by electrophoresis. Biol. Bull. mar. biol. Lab., Woods Hole 155: 193–206

    Google Scholar 

  • Murphy, R. W., Sites, J. W., Buth, D. G., Haufler, C. H. (1990). Proteins. I: Isozyme electrophoresis. In: Hillis, D. M., Moritz, C. (eds.) Molecular systematics. Sinauer, Sunderland, Massachusetts, p. 45–126

    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 

  • O'Foighil, D., Eernisse, D. J. (1988). Geographically widespread, non-hybridizing, sympatric strains of the hermaphroditic, brooding clamLasaea in the northeastern Pacific Ocean. Biol. Bull. mar. biol. Lab., Woods Hole 175: 218–229

    Google Scholar 

  • Palmer, A. R., Gayron, S. D., Woodruff, D. S. (1990). Reproductive, morphological, and genetic evidence for two cryptic species of northeastern PacificNucella. Veliger 33: 325–338

    Google Scholar 

  • SAS Institute, Inc. (1985). SAS user's guide: statistics. Version 5 ed. SAS Institute, Inc., Cary, North Carolina

    Google Scholar 

  • Scheltema, R. S. (1971). Larval dispersal as a means of genetic exchange between geographically separated populations of shallow-water benthic marine gastropods. Biol. Bull. mar. biol. Lab., Woods Hole 140: 284–322

    Google Scholar 

  • Schopf, T. J. M., Murphy, L. S. (1973). Protein polymorphism of the hybridizing seastarsAsterias forbesi andAsterias vulgaris and implications for their evolution. Biol. Bull. mar. biol. Lab., Woods Hole 145: 589–597

    Google Scholar 

  • Sieling, F. W. (1960). A notable range extension of the southern drill,Thais haemastoma floridana, into Chincoteague Bay. Chesapeake Sci. 1: 212–215

    Google Scholar 

  • Sneath, P. H. A., Sokal, R. R. (1973). Numerical taxonomy — the principles and practice of numerical classification. W. H. Freeman & Co., San Francisco

    Google Scholar 

  • Spight, T. M. (1977). Latitude, habitat, and hatching type for muricacean gastropods. Nautilus 91: 67–71

    Google Scholar 

  • St. Amant, L. S. (1938). Studies on the biology of the Louisiana oyster drillThais floridana haysae Clench. M. S. thesis. Louisiana State University, Baton Rouge

    Google Scholar 

  • Staub, K. C., Woodruff, D. S., Upatham, E. S., Viyanant, V. (1990). Genetic variation inNeotricula aperta, the intermediate snail host ofSchistosoma mekongi: allozyme differences reveal a group of sibling species. Am. malac. Bull. 7: 93–103

    Google Scholar 

  • Steiner, W. W. M., Lisowski, E. A., Osterbur, D. (1977). Biochemical differences in sympatric color morphs of an aquatic isopod (Asellus brevicauda). Comp. Biochem. Physiol. 56B: 371–374

    Google Scholar 

  • Strathmann, R. R., Strathmann, M. F., Emson, R. H. (1984). Does limited brood capacity link adult size, brooding, and simultaneous hermaphroditism? A test with the starfishAsterina phylactica. Am. Nat. 123: 796–818

    Article  Google Scholar 

  • Thorpe, J. P., Beardmore, J. A., Ryland, J. S. (1978). Genetic evidence for cryptic speciation in the marine bryozoanAlcyonidium gelatinosum. Mar. Biol. 49: 27–32

    Article  Google Scholar 

  • Tuttle, R. D., Lindahl, R. (1980). Genetic variability in 3 co-occurring forms of the starfish genusOthilia (=Echinaster). Experientia 36: 923–925

    Article  Google Scholar 

  • Walker, R. L. (1982). The gastropodThais haemastoma in Georgia:T. h. floridana orT. h. canaliculata? Gulf Res. Rep. 7: 183–184

    Google Scholar 

  • Weir, B. S., Cockerham, C. C. (1984). EstimatingF-statistics for the analysis of population structure. Evolution 38: 1358–1370

    Google Scholar 

  • Wiley, E. O. (1981). Phylogenetics — the theory and practice of phylogenetic systematics. John Wiley & Sons, New York

    Google Scholar 

  • Williams, A. B., Felder, D. L. (1986). Analysis of stone crabs:Menippe mercenaria (Say), restricted, and a previously unrecognized species described (Decapoda: Xanthidae). Proc. biol. Soc. Wash. 99: 517–543

    Google Scholar 

  • Woodruff, D. S., Staub, K. C., Upatham, E. S., Viyanant, V., Yuan, H.-C. (1988). Genetic variation inOncomelania hupensis:Schistosoma japonicum transmitting snails in China and the Philippines are distinct species. Malacologia 29: 347–361

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

Communicated by J.M. Lawrence, Tampa

Rights and permissions

Reprints and permissions

About this article

Cite this article

Liu, L.L., Foltz, D.W. & Stickle, W.B. Genetic population structure of the southern oyster drillStramonita (=Thais)haemostoma . Mar. Biol. 111, 71–79 (1991). https://doi.org/10.1007/BF01986348

Download citation

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF01986348

Keywords

Navigation