Loss of genetic variation in geographically marginal populations of Atriplex tatarica (Chenopodiaceae)

. 2005 Oct ; 96 (5) : 901-12. [epub] 20050817

Jazyk angličtina Země Velká Británie, Anglie Médium print-electronic

Typ dokumentu časopisecké články, práce podpořená grantem

Perzistentní odkaz   https://www.medvik.cz/link/pmid16107428

BACKGROUND AND AIMS: Genetic variability was estimated for Atriplex tatarica from 25 populations in the Czech Republic. Since its north-western range margin is in central Europe, a relationship between marginality and low within-population genetic diversity was tested in accordance with the Central-Marginal Model. METHODS: Population genetic diversity was expressed by assessing patterns of variation at 13 putatively neutral allozyme loci (comprising 30 putative alleles) within and between 25 natural populations of A. tatarica along a north-west-south-east transect in the Czech Republic. KEY RESULTS: Atriplex tatarica is a species of human-made habitats with a mixed mating system and wide geographic distribution. Overall, A. tatarica displayed moderate levels of genetic diversity in comparison with other herbaceous plants. The percentage of loci that were polymorphic was 47.1%, with average values of 1.55, 0.151 and 0.155 for the average number of alleles per polymorphic locus (A), observed heterozygosity (Ho) and expected heterozygosity (He), respectively. There was only weak evidence of inbreeding within populations (FIS=0.031) and significant population differentiation (FST=0.214). Analysis of the data provides no evidence for isolation-by-distance for the whole study area. However, Mantel tests were highly significant for the marginal Bohemian region and non-significant for the central Moravian region. While northern populations of A. tatarica showed significantly lower allelic richness (A=1.462) than populations from the southern part of the study area (A=1.615), they did not differ in observed heterozygosity (Ho), gene diversity (HS), inbreeding within populations (FIS) or population differentiation (FST), despite generally lower values of particular genetic measurements in the marginal region. CONCLUSIONS: Genetic diversity, with the exception of allelic richness, was not significantly lower at the margins of the species' range. This, therefore, provides only weak support for the predictions of the Central-Marginal Model.

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Aellen P. 1960.Atriplex In: Hegi G, ed. Illustrierte Flora von Miteleuropa. München, 3/2: 664–693 [in German].

Arnold ML. 1997.Natural hybridization and evolution. Oxford: Oxford University Press.

Barrett SCH. 1982. Genetic variation in weeds. In: Charudattan R, Walker H, eds. Biological control of weeds with plant pathogens. New York: John Wiley and Sons, 73–98.

Betancourt JL, Schuster WS, Mitton JB, Anderson RS. 1991. Fossil and genetic history of a pinyon pine (Pinus edulis) isolate. Ecology 72: 1685–1697.

Bosbach K, Hurka H. 1981. Biosystematic studies on Capsella bursa-pastoris (Brassicaceaea): enzyme polymorphism in natural populations. Plant Systematics and Evolution 137: 73–94.

Brown AHD, Burdon JJ. 1983. Multilocus diversity in an outbreeding weed, Echium plantagineum L. Australian Journal of Biological Science 36: 503–509.

Broyles SB. 1998. Postglacial migration and the loss of allozyme variation in northern populations of Asclepias exaltata (Asclepiaceae). American Journal of Botany 85: 202–206. PubMed

Chauvet S, van der Velde M, Imbert E, Guillemin ML, Mayol M, Riba M, et al. 2004. Past and current gene flow in the selfing, wind dispersed species Mycelis muralis in western Europe. Molecular Ecology 13: 1391–1407. PubMed

Cole CT. 2003. Genetic variation in rare and common plants. Annual Review of Ecology, Evolution and Systematics 34: 213–237.

Comps B, Thiébaut B, Paule L, Merzead D, Letouzey J. 1990. Allozyme variability in beechwoods (Fagus sylvatica L.) over central Europe: spatial differentiation among and within populations. Heredity 65: 407–417.

Crow JF, Aoki K. 1984. Group selection for a polygenic behavioral trait: estimating the degree of population subdivision. Proceedings of the National Academy of Sciences of the USA 81: 6073–6077. PubMed PMC

Culley TM, Wallace LE, Gengler-Nowak KM, Crawford DJ. 2002. A comparison of two methods of calculating GST, a genetic measure of population differentiation. American Journal of Botany 89: 460–465. PubMed

Da Cunha AB, Dobzhansky T. 1954. A further study of chromosomal polymorphism in Drosophila willistoni in relation to environment. Evolution 8: 119–134.

Ellstrand NC, Schierenbeck KA. 2000. Hybridization as a stimulus for the evolution of invasiveness in plants? In: Ayala FJ, Fitch WM, Clegg MT, eds. Variation and evolution in plants and microorganisms. Washington, DC: National Academy Press, 289–309. PubMed PMC

Franks SJ, Richards CL, Gonzales E, Cousins JE, Hamrick JL. 2004. Multi-scale analysis of Uniola paniculata (Poaceae): a coastal species with linear, fragmented distribution. American Journal of Botany 91: 1345–1351. PubMed

Godt MJW, Hamrick JL. 1991. Genetic variation in Lathyrus latifolius (Leguminosae). American Journal of Botany 78: 1163–1171.

Goodnight CJ. 1987. On the effect of founder events on epistatic genetic variance. Evolution 41: 80–91. PubMed

Goodnight CJ. 1988. Epistasis and the effect of founder events on the additive genetic variance. Evolution 42: 441–454. PubMed

Goudet J. 1995. Fstat version 1·2: a computer program to calculate F-statistics. Journal of Heredity 86: 485–486.

Griffin SR, Barrett SCH. 2004. Genetic variation in Trillium erectum (Melanthiaceae), a widespread forest herb in eastern North America. Canadian Journal of Botany 82: 316–321.

Haddioui A, Baaziz M. 2001. Genetic diversity of natural populations of Atriplex halimus L. in Marocco: an isoenzyme-based overview. Euphytica 121: 99–106.

Hamrick JL, Godt JW. 1996. Effects of life history traits on genetic diversity in plant species. Philosophical Transactions of the Royal Society of London 351: 1291–1298.

Hayward MD, Zaruk MTM. 1982. Allozyme variation in the inbreeding species Lolium temulentum L. Heredity 49: 255–257.

Hewitt GM. 1996. Some genetic consequences of ice ages, and their role in divergence and speciation. Biological Journal of the Linnean Society 58: 247–276.

Hewitt GM. 1999. Post-glacial re-colonization of Europaean biota. Biological Journal of the Linnean Society 68: 87–112.

Hollingsworth ML, Bailey JP. 2000. Evidence for massive clonal growth in the invasive Fallopia japonica (Japanese Knotweed). Botanical Journal of the Linnean Society 133: 463–472.

Ibrahim KM, Nichols RA, Hewitt GM. 1996. Spatial patterns of genetic variation generated by different forms of dispersal during range expansion. Heredity 77: 282–291.

Ingvarsson PK, Olsson K, Ericson L. 1997. Extinction–recolonization dynamics in the mycophagous beetle Phalacrus substriatus Evolution 51: 187–195. PubMed

Jalas J, Suominen J. eds. 1988.Atlas florae Europaeae: distribution of vascular plants in Europe, Volume II. Cambridge: Cambridge University Press.

Jorgensen S, Hamrick JL, Wells PV. 2002. Regional patterns of genetic diversity in Pinus flexilis (Pinaceae) reveal complex species history. American Journal of Botany 89: 792–800. PubMed

Koniuszek JWJ, Verkeij JAC. 1982. Genetic variation in two related annual Senecio species occurring in the same habitat. Genetica 59: 133–137.

Kubetin WR, Schaal BA. 1979. Apportionment of isozyme variability in Polygonum pemsylvanicum (Polygonaceaea). Systematic Botany 4: 148–156.

Levin DA. 1977. The organisation of genetic diversity in Phlox drummondii Evolution 31: 477–494. PubMed

Mahy G, Vekemans X, Jacquemart A, De Sloover J. 1997. Allozyme diversity and genetic structure in south-western population of heather (Calluna vulgaris). New Phytologist 137: 325–334. PubMed

Mandák B. 2003. Distribution of four Atriplex species with different degrees of invasiveness in the Czech Republic. In: Child LE, Brock JH, Brundu G, Prach K, Pyšek P, Wade PM, et al, eds. Plant invasions: ecological threats and management solutions. Leiden: Backhuys Publisher, 313–328.

Mandák B. 2003. Germination requirements of invasive and non-invasive Atriplex species: a comparative study. Flora 198: 45–54.

Mandák B, Bímová K, Pyšek P, Štěpánek J, Plačková I. 2005. Isoenzyme diversity in Reynoutria taxa: escape from sterility by hybridization. Plant Systematics and Evolution 253: 219–230.

Mandák B, Pyšek P, Lysák M, Suda J, Krahulcová A, Bímová K. 2003. Variation in DNA-ploidy levels of Reynoutria taxa in the Czech Republic. Annals of Botany 92: 265–272. PubMed PMC

Miller M. 1997.Tools for population genetic analyses (TFPGA) 1·3: a Windows program for the analysis of allozyme and molecular population genetic data http://bioweb.usu.edu/mpmbio/tfpga.asp (6 Dec. 2004). Website now at http://www.marksgeneticsoftware.net

Nei M. 1973. Analysis of gene diversity in subdivided populations. Proceedings of the National Academy of Sciences of the USA 70: 3321–3323. PubMed PMC

Nei M. 1978. Estimation of average heterozygosity and genetic distance from a small number of individuals. Genetics 89: 583–590. PubMed PMC

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

Novak GF, Mack RN. 1993. Genetic variation in Bromus tectorum (Poaceae): comparison between native and introduced populations. Heredity 71: 167–176.

Osmond CB, Björkman O, Anderson DJ. 1980.Physiological processes in plant ecology – towards a synthesis with Atriplex. Berlin: Springer Verlag.

Pappert RA, Hamrick JL, Donovan LA. 2000. Genetic variation in Pueraria lobata (Fabaceaea), an introduced, clonal, invasive plant of the southeastern United States. American Journal of Botany 87: 1240–1245. PubMed

Persson H, Widén B, Andersson S, Svensson L. 2004. Allozyme diversity and genetic structure of marginal and central populations of Corylus avellana (Betulaceae) in Europe. Plant Systematics and Evolution 244: 157–179.

Rieseberg LH, Raymond O, Rosenthal DM, Lai Z, Livingstone K, Nakazato T, et al. 2003. Major ecological transitions in wild sunflowers facilitated by hybridisation. Science 301: 1211–1216. PubMed

Schiemann K, Tyler T, Widén B. 2000. Allozyme diversity in relation to geographic distribution and population size in Lathyrus vernus (L.) Bernh. (Fabaceae). Plant Systematics and Evolution 225: 119–132.

Schierenbeck KA, Hamrick JL, Mack RN. 1995. Comparison of allozyme variability in a native and an introduced species of Lonicera Heredity 75: 1–9.

Vallejos CE. 1983. Enzyme activity staining. In: Tanksley SD, Orton TJ, eds. Isozyme in plant genetics and breeding, Part A. Amsterdam: Elsevier, 469–516.

Vila M, Weber E, D'Antonio CM. 2000. Conservation implications of invasion by plant hybridization. Biological Invasions 2: 207–217.

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

Wendel JF, Weeden NF. 1989. Visualisation and interpretation of plant isozymes. In: Soltis DE, Soltis PS, eds. Isozymes in plant biology. Portland, OR: Dioscoroides Press, 5–45.

Whitlock MC, McCauley DE. 1990. Some population genetic consequences of colony formation and extinction – genetic correlations within founding groups. Evolution 44: 1717–1724. PubMed

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

Yeh FC, O'Malley DO. 1980. Enzyme variation in natural populations of Douglas fir, Pseudotsuga menziesii (Mibr.) Franco, from British Columbia. 1. Genetic variation in coastal populations. Silvae Genetica 29: 83–92.

Yeh FC, Yang R-C, Boyle T. 1999.POPGENE version 1·32. Microsoft Window-based freeware for population genetic analysis http://www.ualberta.ca/~fyeh/. 6 Dec. 2004.

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