Population dynamics of diploid and hexaploid populations of a perennial herb
Jazyk angličtina Země Anglie, Velká Británie Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
17881342
PubMed Central
PMC2759246
DOI
10.1093/aob/mcm204
PII: mcm204
Knihovny.cz E-zdroje
- MeSH
- Asteraceae genetika růst a vývoj MeSH
- diploidie * MeSH
- polyploidie * MeSH
- populační dynamika MeSH
- populační genetika MeSH
- roční období MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
BACKGROUND AND AIMS: Despite the recent enormous increase in the number of studies on polyploid species, no studies to date have explored the population dynamics of these taxa. It is thus not known whether the commonly reported differences in single life-history traits between taxa of different ploidy levels result in differences in population dynamics. METHODS: This study explores differences in single life-history traits and in the complete life cycle between populations of different ploidy levels and compares these differences with differences observed between different habitat types and years. Diploid and hexaploid populations of a perennial herb, Aster amellus, are used as the study system. Transition matrix models were used to describe the dynamics of the populations, and population growth rates, elasticity values and life-table response experiments were used to compare the dynamics between populations and years. KEY RESULTS: The results indicate that between-year variation in population dynamics is much larger than variation between different ploidy levels and different habitat conditions. Significant differences exist, however, in the structure of the transition matrices, indicating that the dynamics of the different ploidy levels are different. Strong differences in probability of extinction of local populations were also found, with hexaploid populations having higher probability than diploid populations, indicating strong potential differences in persistence of these populations. CONCLUSIONS: This is the first study on complete population dynamics of plants of different ploidy levels. This knowledge will help to understand the ability of new ploidy levels to spread into new areas and persist there, and the interactions of different ploidy levels in secondary contact zones. This knowledge will also contribute to understanding of interactions of different ploidy levels with other plant species or other interacting organisms such as pollinators or herbivores.
Zobrazit více v PubMed
Abbott RJ, Lowe AJ. Origins, establishment and evolution of new polyploid species: Senecio cambrensis and S. eboracensis in the British Isles. Biological Journal of the Linnean Society. 2004;82:467–474.
Alvarez-Buylla ER, Slatkin M. Finding confidence limits on population-growth rates – 3 real examples revised. Ecology. 1994;75:255–260. PubMed
Bayer RJ, Stebbins GL. A revised classification of Antennaria (Asteraceae: Inuleae) of the eastern United States. Systematic Botany. 1982;7:300–313.
Berdahl JD, Ries RE. Development and vigor of diploid and tetraploid Russian wildrye seedlings. Journal of Range Management. 1997;50:80–84.
Brys R, Jacquemyn H, Endels P, De Blust G, Hermy M. The effects of grassland management on plant performance and demography in the perennial herb Primula veris. Journal of Applied Ecology. 2004;41:1080–1091.
Burton TL, Husband BC. Fitness differences among diploids, tetraploids, and their triploid progeny in Chamerion angustifolium: mechanisms of invasibility and implications for polyploid evolution. Evolution. 2000;54:1182–1191. PubMed
Caswell H. Prospective and retrospective perturbation analyses: their roles in conservation biology. Ecology. 2000;81:619–627.
Caswell H. Matrix population models, construction, analysis, and interpretation. Sunderland, MA: Sinauer Associates; 2001.
Colling G, Matthies D. Effects of habitat deterioration on population dynamics and extinction risk of an endangered, long-lived perennial herb (Scorzonera humilis) Journal of Ecology. 2006;94:959–972.
Damman H, Cain ML. Population growth and viability analyses of the clonal woodland herb, Asarum canadense. Journal of Ecology. 1998;86:13–26.
Efron B, Tibshirani RJ. Introduction to the bootstrap. New York: Chapman and Hall; 1994.
Ehrlén J. Demography of the perennial herb Lathyrus vernus.2. Herbivory and population-dynamics. Journal of Ecology. 1995;83:297–308.
Ehrlén J. Fitness components versus total demographic effects: evaluating herbivore impacts on a perennial herb. American Naturalist. 2003;162:796–810. PubMed
Eriksson A, Eriksson O. Population dynamics of the perennial Plantago media in semi-natural grasslands. Journal of Vegetation Science. 2000;11:245–252.
Evans GM, Rees H. Mitotic cycles in dicotyledons and monocotyledons. Nature. 1971;233:350–351. PubMed
Freville H, Colas B, Riba M, Caswell H, Mignot A, Imbert E, Olivieri I. Spatial and temporal demographic variability in the endemic plant species Centaurea corymbosa (Asteraceae) Ecology. 2004;85:694–703.
Gornall RJ, Wentworth JE. Variation in the chromosome number of Parnassia palustris L. in the British-Isles. New Phytologist. 1993;123:383–388.
Griffith AB, Forseth IN. Population matrix models of Aeschynomene virginica, a rare annual plant: implications for conservation. Ecological Applications. 2005;15:222–233.
Husband BC. Constraints on polyploid evolution: a test of the minority cytotype exclusion principle. Proceedings of the Royal Society B: Biological Sciences. 2000;267:217–223. PubMed PMC
Husband BC. The role of triploid hybrids in the evolutionary dynamics of mixed-ploidy populations. Biological Journal of the Linnean Society. 2004;82:537–546.
Jay M, Reynaud J, Blaise S, Cartier D. Evolution and differentiation of Lotus corniculatus/Lotus alpinus populations from French south-western Alps. Evolutionary Trends in Plants. 1991;5:157–160.
Jongejans E, de Kroon H. Space versus time variation in the population dynamics of three co-occurring perennial herbs. Journal of Ecology. 2005;93:681–692.
Kalisz S, McPeek MA. Demography of an age-structured annual – resampled projection matrices, elasticity analyses, and seed bank effects. Ecology. 1992;73:1082–1093.
de Kroon H, van Groenendael J, Ehrlén J. Elasticities: a review of methods and model limitations. Ecology. 2000;81:607–618.
Lindner R, Garcia A. Genetic differences between natural populations of diploid and tetraploid Dactylis glomerata ssp. izcoi. Grass and Forage Science. 1997;52:291–297.
Mandáková T, Münzbergová Z. Distribution and ecology of Aster amellus aggregates in the Czech Republic. Annals of Botany. 2006;98:845–856. PubMed PMC
Masterson J. Stomatal size in fossil plants – evidence for polyploidy in majority of angiosperms. Science. 1994;264:421–424. PubMed
Merxmüller H, Schreiber A, Yeo PF. Aster. In: Tutin TG, Heywood VH, Burges NA, Valentine DH, Walters SM, Webb DA, editors. Flora Europaea. Vol. 4. New York: Cambridge University Press; 1976.
Meusel H, Jäger E. Vergleichende chorologie der Zentraleuropäischen flora. Jena: Gustav Fischer Verlag; 1992.
Münzbergová Z. Effect of spatial scale on factors limiting species distributions in dry grassland fragments. Journal of Ecology. 2004;92:854–867.
Münzbergová Z. Determinants of species rarity: population growth rates of species sharing the same habitat. American Journal of Botany. 2005;92 1987–1994. PubMed
Münzbergová Z. Effect of population size on prospect of species survival. Folia Geobotanica. 2006;a 41:137–150.
Münzbergová Z. Ploidy level interacts with population size and habitat conditions to determine degree of herbivory damage in plant populations. Oikos. 2006;b 115:443–452.
Münzbergová Z. No effect of ploidy level in plant response to competition in a common garden experiment. Biological Journal of the Linnean Society. 2007 in press.
Münzbergová Z, Ehrlén J. How best to collect demographic data for PVA models. Journal of Applied Ecology. 2005;42:1115–1120.
Nordbakken JF, Rydgren K, Okland RH. Demography and population dynamics of Drosera anglica and D. rotundifolia. Journal of Ecology. 2004;92:110–121.
Oostermeijer JGB, Brugman ML, De Boer ER, Den Nijs HCM. Temporal and spatial variation in the demography of Gentiana pneumonanthe, a rare perennial herb. Journal of Ecology. 1996;84:153–166.
Petit C, Thompson JD. Variation in phenotypic response to light availability between diploid and tetraploid populations of the perennial grass Arrhenatherum elatius from open and woodland sites. Journal of Ecology. 1997;85:657–667.
Petit C, Thompson JD, Bretagnolle F. Phenotypic plasticity in relation to ploidy level and corm production in the perennial grass Arrhenatherum elatius. Canadian Journal of Botany-Revue Canadienne de Botanique. 1996;74 1964–1973.
Pfeifer M, Wiegand K, Heinrich W, Jetschke G. Long-term demographic fluctuations in an orchid species driven by weather: implications for conservation planning. Journal of Applied Ecology. 2006;43:313–324.
Rausch JH, Morgan MT. The effect of self-fertilization, inbreeding depression, and population size on autopolyploid establishment. Evolution. 2005;59:1867–1875. PubMed
Silvertown J, Franco M, Pisanty I, Mendoza A. Comparative plant demography – relative importance of life-cycle components to the finite rate of increase in woody and herbaceous perennials. Journal of Ecology. 1993;81:465–476.
Soltis PS. Ancient and recent polyploidy in angiosperms. New Phytologist. 2005;166:5–8. PubMed
Stebbins GL. Variation and evolution in plants. New York: Columbia University Press; 1950.
Stebbins GL. Polyploidy, hybridization and the invasion of new habitats. Annals of the Missourii Botanical Garden. 1985;72:824–832.
Thompson JN, Cunningham BM, Segraves KA, Althoff DM, Wagner D. Plant polyploidy and insect/plant interactions. American Naturalist. 1997;150:730–743. PubMed
Tyler B, Borrill M, Chorlton K. Studies in Festuca. 10. Observations on germination and seedling cold tolerance in diploid Festuca pratensis and tetrapoid F. pratensis var. apennina in relation to their altitudinal distribution. Journal of Applied Ecology. 1978;15:219–226.
Van't Hof J, Sparrow AH. A relatiohsip between DNA content, nuclear volume, and minimum cell cycle time. Proceedings of the National Academy of Sciences, USA. 1963;49:897–902. PubMed PMC
Vega E, Montana C. Spatio-temporal variation in the demography of a bunch grass in a patchy semiarid environment. Plant Ecology. 2004;175:107–120.
Weppler T, Stoll P, Stocklin J. The relative importance of sexual and clonal reproduction for population growth in the long-lived alpine plant Geum reptans. Journal of Ecology. 2006;94:869–879.
Unmasking cryptic biodiversity in polyploids: origin and diversification of Aster amellus aggregate
Contrasting effects of ploidy level on seed production in a diploid tetraploid system
Comparative population dynamics of two closely related species differing in ploidy level
Niche differentiation between diploid and hexaploid Aster amellus