Skip to main content
Log in

Gene flow among vestimentiferan tube worm (Riftia pachyptila) populations from hydrothermal vents of the eastern Pacific

  • Published:
Marine Biology Aims and scope Submit manuscript

Abstract

Allozyme data are presented for six discrete populations of the giant hydrothermal vent tube worm Riftia pachyptila Jones, 1981 collected throughout the species' known range along mid-ocean spreading ridges of the eastern Pacific Ocean. Contrary to an earlier report, levels of genetic variation are relatively high in this species. Estimates of gene flow based on F-statistics revealed that dispersal throughout the surveyed region is sufficiently high to counter random processes that would lead to losses of genetic diversity and significant population differentiation. R. pachyptila, like other species of tube worms, displays considerable morphologic variation among populations, but this diversity is not reflected in allozyme variation. Vestimentifera, in general, appear to show extensive phenotypic plasticity. In the light of the available genetic data, caution is warranted when making inferences about the taxonomic status of collections based on morphological variation alone. A general decrease in estimated rates of gene flow between geographically more distant populations supports the hypothesis that dispersal in this species follows a stepping-stone model, with exchange between neighboring populations in great excess of long-distance dispersal. High levels of gene flow have been recorded in a variety of vent fauna and may be a prerequisite for success of species found in the ephemeral habitats associated with regions of sea-floor hydrothermal activity.

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

  • Aebersold PB, Winans GA, Teel DJ, Milner GB, Utter FM (1987) Manual for starch gel electrophoresis: a method for the detection of genetic variation. U. S. Department of Commerce, National Oceanic and Atmospheric Administration, National Marine Fisheries Service

  • Black MB (1991) Genetic (allozyme) variation in Vestimentifera (Ridgeia spp.) from hydrothermal vents of the Jaun de Fuca Ridge (Northeast Pacific Ocean). M. Sci. thesis, University of Victoria, BC, Canada

    Google Scholar 

  • Bucklin A (1988) Allozymic variability of Riftia pachyptila populations from the Galápagos Rift and 21°N hydrothermal vents. Deep-Sea Res 35:1759–1768

    Google Scholar 

  • Cary, SC, Felbeck H, Holland ND (1989) Observations on the reproductive biology of the hydrothermal vent tube worm Riftia pachyptila. Mar Ecol Prog Ser 52:89–94

    Google Scholar 

  • Clayton JW, Tretiak DN (1972) Amine-citrate buffers for pH control in starch gel electrophoresis. J Fish Res Bd Can 29:1169–1172

    Google Scholar 

  • Elston RC, Forthofer R (1977) Testing for Hardy-Weinberg equilibrium in small samples. Biometrics 33:536–542

    Google Scholar 

  • France SC, Hessler RR, Vrijenhoek RC (1992) Genetic differentiation between spatially-disjunct populations of the deep-sea, hydrothermal vent-endemic amphipod Ventiella sulfuris. Mar Biol 11:551–559

    Google Scholar 

  • Gilpin ME (1991) The genetic effective size of a metapopulation. Biol J Linn Soc 42:165–175

    Google Scholar 

  • Grassle JF (1986) The ecology of deep-sea hydrothermal vent communities. Adv mar Biol 23:301–362

    Google Scholar 

  • Grassle JP (1985) Genetic differentiation in populations of hydrothermal vent mussels (Bathymodiolus thermophilus) from the Galápagos Rift and 13°N on the East Pacific Rise. Bull biol Soc Wash 64:429–442

    Google Scholar 

  • Haymon RM, Fornari DJ, Von Damm KL, Lilley MD, Perfit MR, Edmonds JM, Shanks WC III, Lutz RA, Grebmair JM, Carbotte S, Wright D, McLaughlin E, Smith M, Beedle N, Olson E (1993) Volcanic eruption of the mid-ocean ridge along the East Pacific Rise crest at 9°45–52′N: direct submersible observations of sea-floor phenomena associated with an eruption event in April, 1991. Earth planet Sci Lett 119:85–101

    Google Scholar 

  • International Union of Biochemistry (1984) Enzyme nomenclature. Academic Press, New York, NY

    Google Scholar 

  • Jones M (1984) The giant tube worms. Oceanus 27:47–52

    Google Scholar 

  • Jones ML (1981) Riftia pachyptila, new genus, new species, the vestimentiferan worm from the Galapagos Rift geothermal vents (Pogonophora). Proc biol Soc Wash 93:1295–1313

    Google Scholar 

  • Jones ML (1985) On the Vestimentifera, new phylum: six new species, and other taxa, from hydrothermal vents and elsewhere. Bull biol Soc Wash 6:117–158

    Google Scholar 

  • Jones ML, Gardiner SL (1989) On the early development of the vestimentiferan tube worm Ridgea sp. and Riftia pachyptila. Biol Bull mar biol Lab, Woods Hole 177:254–276

    Google Scholar 

  • Kimura M, Weiss WH (1964) The stepping stone model of genetic structure and the decrease of genetic correlation with distance. Genetics, Princeton 49:561–576

    Google Scholar 

  • Levene H (1949) On a matching problem arising in genetics. Ann math Statist 20:91–94

    Google Scholar 

  • Li CC, Horvitz DG (1953) Some methods of estimating the inbreeding coefficient. Am J hum Genet 95:107–117

    Google Scholar 

  • Lutz RA (1988) Dispersal of organisms at deep-sea hydrothermal vents: a review. Oceanol Acta (Spec Vol) 8:23–30

    Google Scholar 

  • Lutz RA, Bouchet P, Jablonski D, Turner RD, Waren A (1986) Larval ecology of mollusks at deep-sea hydrothermal vents. Am malac Bull 4:49–54

    Google Scholar 

  • Malécot G (1968) The mathematics of heredity. W. H. Freeman & Co., San Francisco

    Google Scholar 

  • Maruyama T, Kimura M (1980). Genetic variabilityand effective population size when local extinciton and recolonization of subpopulations are frequent. Proc natn Acad Sci USA 77:6710–6714

    Google Scholar 

  • Murphy RW, Sites JW Jr, Buth DG, Haufler CH (1990) Proteins I: Isozyme electrophoresis. In: Hillis D, Moritz C (eds) Molecular systematics. Sinauer Assoc. Inc., Sunderland, Massachusetts, pp 45–126

    Google Scholar 

  • Nei M (1973) Analysis of gene diversity in subdivided populations. Proc natn Acad Sci USA 70:3321–3323

    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, Chesser RK (1983) Estimation of fixation indices and gene diversities. Ann hum Genet 47:253–259

    Google Scholar 

  • Nei M, Maruyama T, Chakraborty R (1975) The bottleneck effect and genetic variability in populations. Evolution 29:1–10

    Google Scholar 

  • Nevo E, Beiles A, Ben-Shlomo R (1983) The evolutionary significance of genetic diversity: ecological, demographic and life history correlates. Lecture Notes Biomaths 53:13–213

    Google Scholar 

  • Rona PA (1987) Oceanic ridge crest processes. Rev Geophys 25:1089–1114

    Google Scholar 

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

    Google Scholar 

  • Slatkin M (1977) Gene flow and genetic drift in a species subject to frequent local extinctions. Theor Popul Biol 12:253–262

    Google Scholar 

  • Slatkin M (1993) Isolation by distance in equilibrium and non-equilibrium populations. Evolution 47:264–279

    Google Scholar 

  • Sokal RR, Wartenberg DE (1983) A test of spatial autocorrelation analysis using an isolation-by-distance model. Genetics, Austin, Tex 105:219–237

    Google Scholar 

  • Southward EC (1988) Development of the gut and segmentation of newly settled stages of Ridgeia (Vestimentifera): implications for relationship between Vestimentifera and Pogonophora. J mar Biol Ass UK 68:465–487

    Google Scholar 

  • Swofford DL, Selander RK (1981) BIOSYS-1: a Fortran program for the comprehensive analysis of electrophoretic data in population genetics and systematics. J Hered 72:281–283

    Google Scholar 

  • Thorpe JP (1983) Enzyme variation, genetic distance and evolutinary divergence in relation to levels of taxonomic separation. In: Oxford GS, Rollinson D (eds) Protein polymorphism: adaptive and taxonomic significance. Academic Press, New York, pp 131–152

    Google Scholar 

  • Tunnicliffe V (1988) Biogeography and evolution of hydrothermalvent fauna in the eastern Pacific Ocean. Proc R Soc (Ser B) 233:347–366

    Google Scholar 

  • Tunnicliffe V (1991) The biology of hydrothermal vents: ecology and evolution. Oceanogr mar Biol A Rev 29:319–407

    Google Scholar 

  • Wade MJ, McCauley DE (1988) Extinction and recolonization: their effects on the genetic differentiation of local populations. Evolution 42:995–1005

    Google Scholar 

  • Weir BS, Cockerham CC (1984) Estimating F-statistics for the analysis of population structure. Evolution 38:1358–1370

    Google Scholar 

  • Workman PL, Niswander JD (1970) Population studies on South-western Indian tribes. II. Local genetic differentiation in the Papago. Am J hum Genet 22:24–49

    Google Scholar 

  • Wright S (1931) Evolution in Mendelian populations. Genetics, Princeton 16:97–159

    Google Scholar 

  • Wright S (1943) Isolation by distance. Genetics, Princeton 28: 114–138

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

Communicated by N. H. Marcus, Tallahassee

Rights and permissions

Reprints and permissions

About this article

Cite this article

Black, M.B., Lutz, R.A. & Vrijenhoek, R.C. Gene flow among vestimentiferan tube worm (Riftia pachyptila) populations from hydrothermal vents of the eastern Pacific. Mar. Biol. 120, 33–39 (1994). https://doi.org/10.1007/BF00381939

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00381939

Keywords

Navigation