Hostname: page-component-78c5997874-dh8gc Total loading time: 0 Render date: 2024-11-19T14:13:12.996Z Has data issue: false hasContentIssue false

High genetic similarity between geographically distant populations in a sea anemone with low dispersal capabilities

Published online by Cambridge University Press:  09 October 2019

A.M. Cava-Solé
Affiliation:
Department of Environmental and Evolutionary Biology, The University of Liverpool, Port Erin Marine Laboratory, Port Erin, Isle of Man. Departamento de Genética, Instituto de Biologia, Universidade Federal do Rio de Janeiro, Bloco A, CCS, Cidade Universitária, Ilha do Fundão, 21.941-Rio de Janeiro-RJ, Brazil.
J.P. Thorpe
Affiliation:
Department of Environmental and Evolutionary Biology, The University of Liverpool, Port Erin Marine Laboratory, Port Erin, Isle of Man.
C.D. Todd
Affiliation:
Gatty Marine Laboratory, Department of Biology and Preclinical Medicine, University of St Andrews, St Andrews, Fife, Scotland, KY16 8LB

Abstract

Samples of the large sublittoral sea anemone Urticina eques (Gosse) were collected from three localities in the northern North Sea and from one locality in the northern Irish Sea. Around the coast the total distance between sampling sites is approximately 1,200 km. The species has a large lecithotrophic larva which may not be planktonic. All samples were screened genetically for 13 loci coding for 11 different enzymes. Results overall indicated a high degree of genetic uniformity over the four populations sampled (FST = 0·025). The data are discussed in relation to current ideas of larval dispersal and results from other similar studies. It is concluded that the lack of genetic differentiation shown by Urticina eques is surprising given the apparently poor dispersive powers of the larva.

Type
Research Article
Copyright
Copyright © Marine Biological Association of the United Kingdom 1994

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Anon., , 1981. Atlas of the seas around the British Isles. Lowestoft: Ministry of Agriculture, Fisheries and Food.Google Scholar
Avise, J.C., 1994. Molecular markers, natural history and evolution. London: Chapman and Hall.Google Scholar
Ayre, D.J., 1984. The effects of sexual and asexual reproduction on geographic variation in the sea anemone Actinia tenebrosa . Oecologia, 62, 222229.Google Scholar
Ayre, D.J., Read, J. & Wishart, J., 1991. Genetic subdivision within the eastern Australian population of the sea anemone Actinia tenebrosa . Marine Biology, 109, 379390.Google Scholar
Carlgren, O., 1906. Die Actinien-larven. Nordisches Plankton, 6, 6589.Google Scholar
Carlgren, O., 1924. Die larven der Ceriantherien, Zoantharien und Actiniarien der Deutschen Tiefsee-Expedition mit einem Nachtrag zu den Zoantharien. Wissenschaftliche Ergebnisse der Deutschen Tiefsee-Expedition, aufdem Dampfer ‘Vivaldia', 1898–1899, 19, 342476.Google Scholar
Carter, M.A. & Miles, J., 1989. Gametogenic cycles and reproduction in the beadlet sea anemone Actinia equina (Cnidaria: Anthozoa). Biological Journal of the Linnean Society of London, 36, 129155.Google Scholar
Chia, F.-S., 1976. Sea anemone reproduction: patterns and adaptive radiations. In Coelenterate ecology and behavior (ed. Mackie, G.O.), pp. 261270. New York: Plenum Press.Google Scholar
Chia, F.-S. & Spaulding, J.G., 1972. Development and juvenile growth of the sea anemone, Tealia crassicornis. Biological Bulletin . Marine Biological Laboratory, Woods Hole, 142, 206218.Google Scholar
Endler, J.A., 1973. Gene flow and population differentiation. Science, New York, 179, 243250.Google Scholar
Hedgecock, D., 1986. Is gene flow from pelagic larval dispersal important in the adaptation and evolution of marine invertebrates? Bulletin of Marine Science, 39, 550564.Google Scholar
Hunt, A. & Ayre, D.J., 1989. Population structure in the sexually reproducing sea anemone Oulactis muscosa . Marine Biology, 102, 537544.Google Scholar
Jokiel, P.L., 1987. Ecology, biogeography and evolution of corals in Hawaii. Trends in Ecology and Evolution, 2, 179182.Google Scholar
Jokiel, P.L., 1989. Rafting of reef corals and other organisms at Kwajalein Atoll. Marine Biology, 101, 483493.Google Scholar
Knowlton, N. & Keller, B.D., 1986. Larvae which fall far short of their potential: highly localized recruitment in an alpheid shrimp with extended larval development. Bulletin of Marine Science, 39, 213223.Google Scholar
Manuel, R.L., 1988. British Anthozoa . Leiden: E.J. Brill. [Synopses British Fauna (New Series) no. 18 (revised).]Google Scholar
Maynard Smith, J., 1989. Evolutionary genetics. Oxford University Press.Google Scholar
McCave, I.N., Caston, V.N.D. & Fannin, N.G.T., 1977. The Quaternary of the North Sea. In British Quaternary studies (ed. Shotton, F.W.), pp. 187204. Oxford University Press.Google Scholar
Nei, M., 1978. Estimation of average heterozygosity and genetic distance from a small number of individuals. Genetics, 89, 583590.Google Scholar
Nei, M., 1987. Molecular evolutionary genetics. New York: Columbia University Press.Google Scholar
Russo, C.A.M., Solé-Cava, A.M. & Thorpe, J.P., 1994. Population structure and genetic variation in two tropical sea anemones (Cnidaria, Actinidae) with different reproductive strategies. Marine Biology, 119, 267276.Google Scholar
Shick, J.M., 1991. A functional biology of sea anemones. London: Chapman and Hall.Google Scholar
Skibinski, D.O.F. & Ward, R.D., 1981. Relationship between allozyme heterozygosity and rates of divergence. Genetical Research, 38, 7192.Google Scholar
Slatkin, M., 1985. Gene flow in natural populations. Annual Review of Ecology and Systematics, 16, 393430.Google Scholar
Slatkin, M., 1987. Gene flow and the geographic structure of natural populations. Science, New York, 236, 787792.Google Scholar
Sneath, P.H.A. & Sokal, R.R., 1973. Numerical taxonomy: the principles and practice of numerical taxonomy. San Francisco: Freeman Press.Google Scholar
Solé-Cava, A.M. & Thorpe, J.P., 1992. Genetic divergence between colour morphs in populations of the common intertidal sea anemones Actinia eauina and A. prasina (Anthozoa: Actiniaria) in the Isle of Man. Marine Biology, 112, 243252.Google Scholar
Solé-Cava, A.M., Thorpe, J.P. & Kaye, J.G., 1985. Reproductive isolation with little genetic divergence between Urticina (= Tealia) felina and U. eaues (Anthozoa: Actiniaria). Marine Biology, 85, 279284.Google Scholar
Stephenson, T.A., 1935. The British sea anemones, vol. 2. London: Ray Society.Google Scholar
Strathmann, R.R., 1985. Feeding and non feeding larval development and life history evolution in marine invertebrates. Annual Review of Ecology and Systematics, 16, 339361.Google Scholar
Swofford, D.L. & Selander, R.K., 1981. BIOSYS-1: a FORTRAN program for the comprehensive analysis of electrophoretic data in population genetics and systematics. Journal of Heredity, 72, 281283.Google Scholar
Thorpe, J.P., 1979. Enzyme variation and taxonomy: the estimation of sampling errors in measures of interspecific genetic similarity. Biological Journal of the Linnean Society of London, 11, 369386.Google Scholar
Thorpe, J.P., 1982. The molecular clock hypothesis: biochemical evolution, genetic differentiation and systematics. Annual Review of Ecology and Systematics, 13, 139168.Google Scholar
Todd, C.D., 1985. Reproductive strategies of north temperate rocky shore invertebrates. In The ecology of rocky coasts: essays presented to J.R. Lewis (ed. Moore, P.G. and Seed, R.), pp. 203219. London: Hodder and Stoughton.Google Scholar
Todd, C.D., Havenhand, J.N. & Thorpe, J.P., 1988. Genetic differentiation, pelagic larval transport and gene flow between local populations of the intertidal marine mollusc Adalaria proxima (Alder and Hancock). Functional Ecology, 2, 441451.Google Scholar
Todd, C.D., Lambert, W.J. & Thorpe, J.P., 1994. The genetic structure of intertidal populations of two species of mollusc on the Scottish west coast: some biogeographic considerations and an assessment of realized larval dispersal. In The islands of Scotland: a living marine heritage (ed. Baxter, J. and Usher, M.B.), pp. 6788. Edinburgh: Scottish Natural Heritage.Google Scholar
Todd, C.D., Thorpe, J.P. & Hadfield, M.G., 1991. Genetic structure of populations of the aplysiid opisthobranch Stylocheilus longicaudus (Quoy & Gaimard) around the shores of O'Ahu, Hawaii. Journal of Molluscan Studies, 57(4) supplement, 153166.Google Scholar
Wright, S., 1978. Evolution and the genetics of populations. Vol. 4. Variability within and among natural populations . Chicago: University of Chicago Press.Google Scholar