Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

Advertisement

Heredity
  • View all journals
  • Search
  • Log in
  • Content Explore content
  • About the journal
  • Publish with us
  • Sign up for alerts
  • RSS feed
  1. nature
  2. heredity
  3. original article
  4. article
Genetic variation in continental and island populations of Eichhornia paniculata (Pontederiaceae)
Download PDF
Download PDF
  • Original Article
  • Published: 01 August 1987

Genetic variation in continental and island populations of Eichhornia paniculata (Pontederiaceae)

  • D E Glover1 nAff2 &
  • S C H Barrett1 

Heredity volume 59, pages 7–17 (1987)Cite this article

  • 720 Accesses

  • 66 Citations

  • Metrics details

Abstract

Genetic variation was examined at 21 allozyme loci in 11 populations of Eichhornia paniculata (Pontederiaceae) from N.E. Brazil and Jamaica. Populations from Jamaica are genetically depauperate with respect to electrophoretically detectable variation, containing a significantly lower number of polymorphic loci, alleles per locus, mean observed heterozygosity and genetic diversity than Brazilian populations. These measures were significantly correlated with the outcrossing rate (t) of populations. The allozyme data were used to examine the patterns of genetic variation within and between populations by estimates of gene correlation and Nei's gene diversity statistics. Populations within both regions are highly differentiated from one another, with those from Jamaica more strongly so. Brazilian populations contain more variation than is distributed among populations, while the reverse pattern occurs among Jamaican populations. The genetic distance between Jamaican populations is less than between Brazilian populations as a result of the low overall variability on the island. It is proposed that the founding of populations on Jamaica by long-distance dispersal, genetic drift and high levels of self-fertilisation all contribute to reducing levels of genetic variation in Jamaican populations.

Similar content being viewed by others

Chromosome evolution and the genetic basis of agronomically important traits in greater yam

Article Open access 14 April 2022

Transcriptome-wide analysis of introgression-resistant regions reveals genetic divergence genes under positive selection in Populus trichocarpa

Article 19 November 2020

Accumulating candidate genes for broad-spectrum resistance to rice blast in a drought-tolerant rice cultivar

Article Open access 02 November 2021

Article PDF

References

  • Avise, J C, Smith, M H, Selander, R K, Lawlor, T E, and Ramsey, P R. 1974. Biochemical polymorphism and systematics in the genus Peromyscus, V: Insular and mainland species of the subgenus Hapolomyomys. Syst Zool, 23, 226–238.

    Article  Google Scholar 

  • Ayala, F J, Powell, J R, and Dobzhansky, T. 1971. Enzyme variability in the Drosophila willistoni group. II. Polymorphisms in continental and island populations of Drosophila willistoni. Proc Nat Acad Sci USA, 68, 2480–2483.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Baker, H G. 1955. Self-compatibility and establishment after “long-distance” dispersal. Evolution, 9, 347–348.

    Google Scholar 

  • Barrett, S C H. 1979. The evolutionary breakdown of tristyly in Eichhornia crassipes (Mart.) Solms (Water Hyacinth). Evolution, 33, 449–510.

    Article  Google Scholar 

  • Barrett, S C H. 1985a. Floral trimorphism and monomorphism in continental and island populations of Eichhornia paniculata (Spreng.) Solms. (Pontederiaceae). Biol J Linn Soc, 25, 41–60.

    Article  Google Scholar 

  • Barrett, S C H. 1985b. Ecological genetics of breakdown in tristyly. In Haeck, J. and J. W. Woldendorp (eds.) Structure and Functioning of Plant Populations 2: Phenotypic and Genotypic Variation in Plant Populations. North-Holland Publishing Company, Amsterdam, pp. 267–275.

    Google Scholar 

  • Barrett, S C H, Brown, A H D, and Shore, J S. 1987. Disassortative mating in tristylous Eichhornia paniculata (Pontederiaceae). Heredity, 58, 49–55.

    Article  Google Scholar 

  • Bosbach, K, and Hurka, H. 1981. Biosystematic studies on Capsella bursapastoris (Brassicaceae): Enzyme polymorphism in natural populations. Plant Syst and Evol 137, 73–94.

    Article  CAS  Google Scholar 

  • Brown, A H D. 1979. Enzyme polymorphism in plant populations. Theor Pop Biol, 15, 1–42.

    Article  Google Scholar 

  • Brown, A H D, and Marshall, D R. 1981. Evolutionary changes accompanying colonization in plants. In Scudder, G. C. E. and Reveal, J. L. (Eds.) Evolution Today. Carnegie-Mellon University, Pittsburgh, pp. 351–363.

    Google Scholar 

  • Brown, C R, and Jain, S K. 1979. Reproductive system and pattern of genetic variation in two Limnanthes species. Theor and Appl Genet, 54, 181–190.

    Article  CAS  Google Scholar 

  • Cardy, B J, Stuber, C W, and Goodman, M M. 1981. Techniques for starch gel electrophoresis of enzymes from maize (Zea mays L.). Institute of Statistics Mimeograph Series No. 1317, North Carolina State University, Raleigh, 31 pp.

  • Carlquist, S. 1974. Island Biology. Columbia Press, New York.

    Book  Google Scholar 

  • Clarke, C A, and Sheppard, P M. 1963. Interactions between major genes and polygenes in the determination of the mimetic patterns of Papilio dardanus. Evolution, 17, 404–413.

    Article  Google Scholar 

  • Cockerham, C C. 1969. Variance of gene frequencies. Evolution, 23, 72–84.

    Article  PubMed  Google Scholar 

  • Cockerham, C C. 1973. Analysis of gene frequencies. Genetics, 74, 679–700.

    CAS  PubMed  PubMed Central  Google Scholar 

  • Darlington, P J. Jr. 1957. Zoogeography. John Wiley and Sons, New York.

    Google Scholar 

  • Dietz, E J. 1983. Permutation tests for association between two distance matrices. Syst Zool, 32, 21–26.

    Article  Google Scholar 

  • Dobzhansky, T. 1957. Genetics of natural populations. XXVI Chromosome variability in island and continental populations of Drosophila willistoni from Central America and the West Indies. Evolution, 11, 280–293.

    Article  Google Scholar 

  • Ganders, F R, Denny, S E, and Tsai, D. 1985. Breeding systems and genetic variation in Amsinckia spectabilis (Boraginaceae). Can J Bot, 66, 533–538.

    Article  Google Scholar 

  • Glover, D E. 1985. Mating systems and genetic variation in continental and island populations of Eichhornia paniculata (Spreng.) Solms (Pontederiaceae). M.Sc. Thesis, University of Toronto.

  • Glover, D E, and Barrett, S C H. 1986. Variation in the mating system of Eichhornia paniculata (Spreng.) Solms (Pontederiaceae). Evolution, 40, 1122–1131.

    Article  PubMed  Google Scholar 

  • Gottlieb, L D. 1973. Enzyme differentiation and phylogeny in Clarkia franciscana, C. rubicunda and C. amoena. Evolution, 27, 205–214.

    Article  CAS  PubMed  Google Scholar 

  • Gottlieb, L D. 1981. Electrophoretic evidence and plant populations. Prog, in Phytochemistry, 7, 1–46.

    CAS  Google Scholar 

  • Guries, R P, and Ledig, F T. 1982. Genetic diversity and population structure in pitch pine (Pinus rigida Mill.). Evolution, 36, 387–402.

    Article  PubMed  Google Scholar 

  • Harding, J, and Mankinen, C B. 1978. Genetics of Lupinus IV. Colonization and genetic variability in Lupinus suc-culentus. Theor Appl Genet, 42, 267–271.

    Article  Google Scholar 

  • Hamrick, J L, Linhart, Y B, and Mitton, J B. 1979. Relationships between life history characters and elec-trophoretically detectable genetic variation in plants. Ann Rev Ecol Syst, 10, 173–200.

    Article  Google Scholar 

  • Jain, S K. 1976. The evolution of inbreeding in plants. Ann Rev Ecol Syst, 7, 469–495.

    Article  Google Scholar 

  • Jain, S K, and Martins, P S. 1979. Ecological genetics of the colonizing ability of rose clover (Trifolium hirtum All.). Amer J Bot, 66, 361–366.

    Article  Google Scholar 

  • Lack, D. 1976. Darwin's Finches. Cambridge University Press, Cambridge.

    Google Scholar 

  • Layton, C R, and Ganders, F R. 1984. The genetic consequences of contrasting breeding systems in Plectritis (Valerianaceae). Evolution, 38, 1308–1325.

    Article  PubMed  Google Scholar 

  • Levin, D A. 1977. The organization of genetic variability in Phlox drummondii. Evolution, 38, 477–494.

    Article  Google Scholar 

  • Levin, D A. 1978. Genetic variation in annual Phlox: Self-compatible versus self-incompatible species. Evolution, 32, 245–263.

    Article  PubMed  Google Scholar 

  • Loveless, M D, and Hamrick, J L. 1984. Ecological determinants of genetic structure in plant populations. Ann Rev Ecol Syst, 15, 65–95.

    Article  Google Scholar 

  • Macarthur, R H, and Wilson, E O. 1967. The Theory of Island Biogeography. Princeton University Press, Princeton.

    Google Scholar 

  • Miller, R G. 1974. The jackknife-a review. Biometrika, 61, 1–15.

    Google Scholar 

  • Mitton, J B, Linhart, Y B, Hamrick, J L, and Beckman, J S. 1977. Observations on the genetic structure and mating system of ponderosa pine in the Colorado front range. Theor Appl Genet, 51, 5–13.

    Article  CAS  PubMed  Google Scholar 

  • Nei, M. 1972. Genetic distance between populations. Amer Natur, 106, 283–292.

    Article  Google Scholar 

  • Nei, M. 1973. Analysis of gene diversity in subdivided populations. Proc Nat Acad Sci, 70, 3321–3323.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Nei, M, and Roychoudhury, A K. 1974. Sampling variances of heterozygosity and genetic distance. Genetics, 76, 379–390.

    CAS  PubMed  PubMed Central  Google Scholar 

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

    Article  PubMed  Google Scholar 

  • Price, S C, and Jain, S K. 1981. Are inbreeders better colonizers? Oecologia, 49, 283–286.

    Article  CAS  PubMed  Google Scholar 

  • Rick, C M, and Fobes, J F. 1975. Allozymes of Galapagos tomatoes: Polymorphism, geographic distribution and affinities. Evolution, 29, 443–457.

    Article  PubMed  Google Scholar 

  • Rick, C M, Fobes, J F, and Holle, M. 1977. Genetic variation in Lycopersicon pimpinellifolium : evidence of evolutionary change in mating systems. Pl Syst Evol, 127, 139–170.

    Article  Google Scholar 

  • Rick, C M, Fobes, J F, and Tanksley, S D. 1979. Evolution of mating systems in Lycopersicon hirsutum as deduced from genetic variation in electrophoretic and morphological characters. Pl Syst Evol, 132, 279–298.

    Article  Google Scholar 

  • Scandalios, J G. 1969. Genetic control of molecular forms of isozymes in plants-a review. Biochem Genet, 3, 37–39.

    Article  CAS  Google Scholar 

  • Schoen, D J. 1982. Genetic variation and the breeding system of Gilia achilleifolia. Evolution, 36, 361–370.

    Article  PubMed  Google Scholar 

  • Schwaegerle, K E, and Schaal, B A. 1979. Genetic variability and founder effect in the pitcher plant Sarracenia purpurea L. Evolution, 33, 1210–1218.

    Article  PubMed  Google Scholar 

  • Shaw, C R, and Prasad, R. 1970. Starch gel electrophoresis of enzymes-A compilation of recipes. Biochem Genet, 3, 207–320.

    Google Scholar 

  • Vallejos, C E. 1983. Enzyme activity staining. In Tanksley, S. D. and Orton, T. J. (Eds.) Isozymes in Plant Genetics and Breeding Part A. Elsevier Science Publishers, B.V. Amsterdam, pp. 469–515.

    Google Scholar 

  • Weir, B S, and Cockerham, C C. 1984. Estimating F-statis-tics for the analysis of population structure. Evolution, 38, 1358–1370.

    CAS  PubMed  Google Scholar 

  • Williamson, M. 1981. Island Populations. Oxford University Press, Oxford.

    Google Scholar 

  • Wright, S. 1951. The genetical structure of populations. Ann Eugen, 15, 313–354.

    Google Scholar 

  • Yeh, F C, and Layton, C R. 1979. The organization of genetic variability in central and marginal populations of lodgepole pine Pinus contorta spp. Latifolia Can J Genet Cytol, 11, 487–503.

    Article  Google Scholar 

Download references

Author information

Author notes
  1. D E Glover

    Present address: Department of Botany and Plant Sciences, University of California, Riverside, California, 92521, U.S.A.

Authors and Affiliations

  1. Department of Botany, University of Toronto, Toronto, M5S 1A1, Ontario, Canada

    D E Glover & S C H Barrett

Authors
  1. D E Glover
    View author publications

    Search author on:PubMed Google Scholar

  2. S C H Barrett
    View author publications

    Search author on:PubMed Google Scholar

Rights and permissions

Reprints and permissions

About this article

Cite this article

Glover, D., Barrett, S. Genetic variation in continental and island populations of Eichhornia paniculata (Pontederiaceae). Heredity 59, 7–17 (1987). https://doi.org/10.1038/hdy.1987.91

Download citation

  • Received: 22 July 1986

  • Issue date: 01 August 1987

  • DOI: https://doi.org/10.1038/hdy.1987.91

Share this article

Anyone you share the following link with will be able to read this content:

Sorry, a shareable link is not currently available for this article.

Provided by the Springer Nature SharedIt content-sharing initiative

This article is cited by

  • Genetic Diversity Within and among Disjunct Populations of the Mediterranean Island Endemic Delphinium pictum and D. requienii (Ranunculaceae)

    • Maria Renée Orellana
    • Cèsar Blanché
    • Maria Bosch

    Folia Geobotanica (2009)

  • Colonisation as a common denominator in plant metapopulations and range expansions: effects on genetic diversity and sexual systems

    • John R. Pannell
    • Marcel E. Dorken

    Landscape Ecology (2006)

  • Legitimate pollination of the tristylous flowers ofEichhornia azurea (Pontederiaceae) byAncyloscelis gigas bees (Anthophoridae, Apoidea)

    • I. Alves Dos Santos
    • D. Wittmann

    Plant Systematics and Evolution (2000)

  • Do island populations have less genetic variation than mainland populations?

    • R Frankham

    Heredity (1997)

  • The successful founder: genetics of introduced Carduelis chloris (greenfinch) populations in New Zealand

    • Juha Merilä
    • Mats Björklund
    • Allan J Baker

    Heredity (1996)

Download PDF

Advertisement

Explore content

  • Research articles
  • Reviews & Analysis
  • News & Comment
  • Podcasts
  • Current issue
  • Collections
  • Follow us on Twitter
  • Sign up for alerts
  • RSS feed

About the journal

  • Journal Information
  • Open access publishing
  • About the Editors
  • Contact
  • About the Partner
  • For Advertisers
  • Subscribe

Publish with us

  • For Authors & Referees
  • Language editing services
  • Open access funding
  • Submit manuscript

Search

Advanced search

Quick links

  • Explore articles by subject
  • Find a job
  • Guide to authors
  • Editorial policies

Heredity (Heredity)

ISSN 1365-2540 (online)

ISSN 0018-067X (print)

nature.com sitemap

About Nature Portfolio

  • About us
  • Press releases
  • Press office
  • Contact us

Discover content

  • Journals A-Z
  • Articles by subject
  • protocols.io
  • Nature Index

Publishing policies

  • Nature portfolio policies
  • Open access

Author & Researcher services

  • Reprints & permissions
  • Research data
  • Language editing
  • Scientific editing
  • Nature Masterclasses
  • Research Solutions

Libraries & institutions

  • Librarian service & tools
  • Librarian portal
  • Open research
  • Recommend to library

Advertising & partnerships

  • Advertising
  • Partnerships & Services
  • Media kits
  • Branded content

Professional development

  • Nature Awards
  • Nature Careers
  • Nature Conferences

Regional websites

  • Nature Africa
  • Nature China
  • Nature India
  • Nature Japan
  • Nature Middle East
  • Privacy Policy
  • Use of cookies
  • Legal notice
  • Accessibility statement
  • Terms & Conditions
  • Your US state privacy rights
Springer Nature

© 2025 Springer Nature Limited