Skip to main content
Log in

Spatial autocorrelation analysis of small-scale genetic structure in a clonal soft coral with limited larval dispersal

  • Published:
Marine Biology Aims and scope Submit manuscript

Abstract

The philopatric larval dispesal and small effective population sizes characteristic of many clonal species should promote the development of significant small-scale genetic structure within populations as a result of isolation-by-distance. We used spatial autocorrelation statistics to detect genetic structure, arising from both clonal reproduction and philopatric dispersal of sexual propagules, for five allozyme loci within populations of the soft coral Alcyonium sp. In a population on Tatoosh Island, Washington, USA, sampled in 1991/1992, we found significant positive spatial autocorrelation at all loci among individuals separated by <40 cm, reflecting the presence of significant smallscale genetic structure due to associations among clonemates. For 4 of 5 loci, however, we detected no significant spatial autocorrelation among the different clones within this population over distances of 1 to 40 m. Analysis of soft-coral populations from six additional, topographically diverse sites in the north-east Pacific also did not reveal significant spatial autocorrelation among clones at any loci. This general lack of spatial autocorrelation of genotypes among clones suggests that significant small-scale genetic structure has not arisen in populations of Alcyonium sp. as a consequence of isolation-by-distance.

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

  • Argyres AZ, Schmitt J (1991) Microgeographic genetic structure of morphological and life history traits in a natural population of Impatiens capensis. Evolution 45: 178–189

    Google Scholar 

  • Ayre DJ (1984) The effects of sexual and asexual reproduction on geographic variation in the sea anemone Actinia tenebrosa. Oecologia 62: 222–229

    Google Scholar 

  • Ayre DJ (1988) Evidence for genetic determination of sex in Actinia tenebrosa. J exp mar Biol Ecol 116: 23–43

    Google Scholar 

  • Ayre DJ, Dufty S (1994) Evidence for restricted gene flow in the viviparous coral Seriatopora hystrix on Australia's Great Barrier Reef. Evolution 48: 1183–1201

    Google Scholar 

  • Ayre DJ, Read J, Wishart J (1991) Genetic subdivision within the eastern Australian population of the sea anemone Actinia tenebrosa. Mar Biol 109: 379–390

    Google Scholar 

  • Ayre DJ, Resing JM (1986) Sexual and asexual production of planulae in reef corals. Mar Biol 90: 187–190

    Google Scholar 

  • Babcock RC (1991) Comparative demography of three species of scleractinian corals using age-and size-dependent classifications. Ecol Monogr 61: 225–244

    Google Scholar 

  • Berg EE, Hamrick JL (1985) Fine-scale genetic structure of a Turkey oak forest. Evolution 49: 110–120

    Google Scholar 

  • Black R, Johnson MS (1979) Asexual viviparity and population genetics of Actinia tenebroasa. Mar Biol 53: 27–31

    Google Scholar 

  • Brazeau DA, Harvell CD (1994) Genetic structure of local populations and divergence between growth forms in a clonal invertebrate, the Caribbean octocoral Briareum asbestinum. Mar Biol 119: 53–60

    Google Scholar 

  • Brazeau DA, Lasker HR (1992) Reproductive success in the Caribbean octocoral Briareum asbestinum. Mar Biol 114: 157–163

    Google Scholar 

  • Burnett WJ, Benzie JAH, Beardmore JA, Ryland JS (1995) Patterns of genetic subdivision in populations of a clonal cnidarian, Zoanthus coppingeri, from the Great Barrier Reef. Mar Biol 122: 665–673

    Google Scholar 

  • Cliff AD, Ord JK (1981) Spatial processes. Pion Ltd., London

    Google Scholar 

  • Coates DJ (1992) Genetic consequences of a bottleneck and spatial genetic structure in the triggerplant Stylidium coroniforme (Stylidiaceae). Heredity, Lond 69: 512–520

    Google Scholar 

  • Coffroth MA, Lasker HR, Diamond ME, Bruenn JA, Bermingham E (1992) DNA fingerprints of a gorgonian coral: a method for detecting clonal structure in a vegetative species. Mar Biol 114: 317–325

    Google Scholar 

  • Crawford TJ (1984) What is a population? In: Shorrocks B (ed) Evolutionary ecology. Blackwell Scientific Publications, Oxford, pp 135–173

    Google Scholar 

  • Denny MW (1988) Biology and the mechanics of the wave-swept environment. Princeton University Press, Princeton, New Jersey

    Google Scholar 

  • Denny MW, Shibata MF (1989) Consequences of surf-zone turbulence for settlement and external fertilization. Am Nat 134: 859–889

    Google Scholar 

  • Dewey SE, Heywood JS (1988) Spatial genetic structure in a population of Psychotria nervosa. I. Distribution of genotypes. Evolution 42: 834–838

    Google Scholar 

  • Endler JA (1977) Geographic variation, speciation, and clines. Princeton University Press, Princeton, New Jersey

    Google Scholar 

  • Epperson BK (1989) Spatial patterns of genetic variation within plant populations. In: Brown AHD, Clegg MT, Kahler AL, Weir BS (eds) Plant population genetics, breeding, and genetic resources. Sinauer Associates, Sunderland, Mass, pp 229–253

    Google Scholar 

  • Epperson BK (1990) Spatial autocorrelation of genotypes under directional selection. Genetics, Austin, Tex 124: 757–771

    Google Scholar 

  • Epperson BK (1995) Spatial distribution of genotypes under isolation by distance. Genetics, Austin, Tex 140: 1431–1440

    Google Scholar 

  • Epperson BK, Allard RW (1989) Spatial autocorrelation analysis of the distribution of genotypes within populations of lodgepole pine. Genetics, Austin, Tex 121: 369–377

    Google Scholar 

  • Epperson BK, Clegg MT (1986) Spatial-autocorrelation analysis of flower color polymorphisms within substructured populations of morning glory (Ipomoea purpurea). Am Nat 128: 840–858

    Google Scholar 

  • Gabriel KR, Sokal RR (1969) A new statistical approach to geographic variation analysis. Syst Zool 18: 259–270

    Google Scholar 

  • Gerrodette T (1981) Dispersal of the solitary coral Balanophyllia elegans by demersal planular larvae. Ecology 62: 611–619

    Google Scholar 

  • Grosberg RK (1991) Sperm-mediated gene flow and the genetic structure of a population of the colonial ascidian Botryllus schlosseri. Evolution 45: 130–142

    Google Scholar 

  • Hartl DL, Clark AG (1988) Principles of population genetics. 2nd edn. Sinauer Associates Inc. Sunderland, Mass

    Google Scholar 

  • Hellberg ME (1995) Stepping-stone gene flow in the solitary coral Balanophyllia elegans: equilibrium and nonequilibrium at different spatial scales. Mar Biol 123: 573–581

    Google Scholar 

  • Hoffmann RJ (1986) Variation in contributions of asexual reproduction to the genetic structure of populations of the sea anemone Metridium senile. Evolution 40: 357–365

    Google Scholar 

  • Hughes TP, Ayre D, Connell JH (1992) The evolutionary ecology of corals. Trends Ecol Evolut 7: 292–295

    Google Scholar 

  • Hunter CL (1993) Genotypic variation and clonal structure in coral populations with different disturbance histories. Evolution 47: 1213–1228

    Google Scholar 

  • Jackson JBC (1985) Distribution and ecology of clonal and aclonal benthic invertebrates. In: Jackson JBC, Buss LW, Cook RE (eds) Population biology and evolution of clonal organisms. Yale University Press, New Haven, pp 297–355

    Google Scholar 

  • Jackson JBC (1986) Modes of dispersal of clonal benthic invertebrates: consequences for species distributions and genetic structure of local populations. Bull mar Sci 39: 588–606

    Google Scholar 

  • Jackson JBC, Coates AG (1986) Life cycles and evolution of clonal (modular) animals. Phil Trans R Soc (Ser B) 313: 7–22

    Google Scholar 

  • Jokiel PL (1984) Long distance dispersal of reef corals by rafting. Coral Reefs 3: 113–116

    Google Scholar 

  • Knowlton N, Jackson JBC (1993) Inbreeding and outbreeding in marine invertebrates. In: Thornhill N (ed) The natural history of inbreeding and outbreeding. University of Chicago Press, Chicago, pp 200–249

    Google Scholar 

  • Levitan DR (1991) Influence of body size and population density on fertilization success and reproductive output in a free-spawning invertebrate. Biol Bull mar biol Lab, Woods Hole 181: 261–268

    Google Scholar 

  • Li CC, Horvitz DG (1953) Some methods of estimating the inbreeding coefficient. Am J hum Genet 5: 107–117

    Google Scholar 

  • Mayr E (1970) Populations, species, and evolution. Harvard University Press, Cambridge, Mass

    Google Scholar 

  • McFadden CS (1986) Colony fission increases particle capture rates of a soft coral: advantages of being a small colony. J exp mar Biol Ecol 103: 1–20

    Google Scholar 

  • McFadden CS (1991) A comparative demographic analysis of clonal reproduction in a temperate soft coral. Ecology 72: 1849–1866

    Google Scholar 

  • McFadden CS (1996) A genetic analysis of clonal reproduction in a temperate soft coral: can population genetic structure be predicted from clonal demography? (In preparation)

  • Mladenov PV, Emson RH (1988) Density, size structure and reproductive characteristics of fissiparous brittle stars in algae and sponges: evidence for interpopulational variation in levels of sexual and asexual reproduction. Mar Ecol Prog Ser 42: 181–194

    Google Scholar 

  • Pennington JT (1985) The ecology of fertilization of echinoid eggs: the consequences of sperm dilution, adult aggregation, and synchronous spawning. Biol Bull mar biol Lab, Woods Hole 169: 417–430

    Google Scholar 

  • Perry DJ, Knowles P (1991) Spatial genetic structure within three sugar maple (Acer saccharum Marsh.) stands. Heredity, Lond 66: 137–142

    Google Scholar 

  • Potts DC (1984) Generation times and the Quaternary evolution of reef-building corals. Paleobiology 10: 48–58

    Google Scholar 

  • Potts DC, Done TJ, Isdale PJ, Fisk DA (1985) Dominance of a coral community by the genus Porites (Scleractinia). Mar Ecol Prog Ser 23: 79–84

    Google Scholar 

  • Schnabel A, Laushmann RH, Hamrick JL (1991) Comparative genetic structure of two co-occurring tree species, Maclura pomifera (Moraceae) and Gleditsia triacanthos (Leguminosae). Heredity, Lond 67: 357–364

    Google Scholar 

  • Schoen DJ, Latta RG (1989) Spatial autocorrelation of genotypes in populations of Impatients pallida and Impatiens capensis. Heredity, Lond 63: 181–189

    Google Scholar 

  • Shapcott A (1995) The spatial genetic structure in natural populations of the Australian temperate rainforest tree Atherosperma moschatum (Labill.) (Monimiaceae). Heredity, Lond 74: 28–38

    Google Scholar 

  • Shick JM, Lamb AN (1977) Asexual reproduction and genetic population structure in the colonizing sea anemone Haliplanella luciae. Biol Bull mar biol Lab, Woods Hole 153: 604–617

    Google Scholar 

  • Sokal RR (1979) Ecological parameters inferred from spatial correlograms. In: Patil GP, Rosenzweig ML (eds) Contemporary quantitative ecology and related ecometrics. International Cooperative Publishing House, Fairland, Md, pp 167–196

    Google Scholar 

  • Sokal RR, Jacquez GM, Wooten MC (1989) Spatial autocorrelation analysis of migration and selection. Genetics, Austin, Tex 121: 845–855

    Google Scholar 

  • Sokal RR, Oden NL (1978a) Spatial autocorrelation in biology. I. Methodology. Biol J Linn Soc 10: 199–228

    Google Scholar 

  • Sokal RR, Oden NL (1978b) Spatial autocorrelation in biology. II. Some biological implications and four applications of evolutionary and ecological interest. Biol J Linn Soc 10: 229–249

    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 

  • Stoddart JA (1983) Asexual production of planulae in the coral Pocillopora damicornis. Mar Biol 76: 279–284

    Google Scholar 

  • Stoddart JA (1984a) Genetical structure within populations of the coral Pocillopora damicornis. Mar Biol 81: 19–30

    Google Scholar 

  • Stoddart JA (1984b) Genetic differentiation amongst populations of the coral Pocillopora damicornis off southwestern Australia. Coral Reefs 3: 149–156

    Google Scholar 

  • Stoddart JA (1988) Historecognition and fine-scale spatial genetic structure in sessile benthic invertebrates. In: Grosberg RK, Hedgecock D, Nelson K (eds) Invertebrate historecognition. Plenum Publishing Corp, New York, pp 111–125

    Google Scholar 

  • Swofford DL, Selander RB (1981) BIOSYS-1: a computer program for the analysis of allelic variation in genetics. University of Illinois at Urbana-Champagne, Urbana, Illinois

    Google Scholar 

  • Turner ME, Stephens JC, Anderson WW (1982) Homozygosity and patch structure in plant populations as a result of nearestneighbor pollination. Proc natn Acad Sci USA 79: 203–207

    Google Scholar 

  • Waser NM (1987) Spatial genetic heterogeneity in a population of the montane perennial plant Delphinium nelsonii. Heredity, Lond 58: 249–256

    Google Scholar 

  • Weir BS (1990) Intraspecific differentiation. In: Hillis DM, Moritz C (eds) Molecular systematics. Sinauer Associates, Sunderland, Mass, pp 373–410

    Google Scholar 

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

    Google Scholar 

  • Williams CF (1994) Genetic consequences of seed dispersal in three sympatric forest herbs. II. Microspatial genetic structure within populations. Evolution 48: 1959–1972

    Google Scholar 

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

    Google Scholar 

  • Wright S (1946) Isolation by distance under diverse systems of mating. Genetics, Princeton 31: 39–59

    Google Scholar 

  • Wright S (1951) The genetical structure of populations. Ann Eugen 15: 323–354

    Google Scholar 

  • Wright S (1965) The interpretation of population structure by F-statistics with special regard to systems of mating. Evolution 19: 395–420

    Google Scholar 

  • Wright S (1969) Evolution and the genetics of populations, Vol 2. The theory of gene frequencies. University of Chicago Press, Chicago

    Google Scholar 

  • Yund PO (1990) An in situ measurement of sperm dispersal in a colonial marine hydroid. J exp Zool 253: 102–106

    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

McFadden, C.S., Aydin, K.Y. Spatial autocorrelation analysis of small-scale genetic structure in a clonal soft coral with limited larval dispersal. Marine Biology 126, 215–224 (1996). https://doi.org/10.1007/BF00347446

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00347446

Keywords

Navigation