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      Distribution and habitat segregation on different spatial scales among diploid, tetraploid and hexaploid cytotypes of Senecio carniolicus (Asteraceae) in the Eastern Alps

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          Abstract

          Background and Aims

          The spatial distribution of cytotypes can provide valuable insights into evolutionary patterns of polyploid complexes. In a previous study the macro-scale distribution of the three main cytotypes in Senecio carniolicus (Asteraceae) within the Eastern Alps was characterized. Employing a roughly 12-fold extended sampling, the present study focuses on unravelling patterns of cytotype distribution on the meso- and microscale and on correlating those with ecological properties of the growing sites.

          Methods

          DAPI flow cytometry of dried samples was used to determine DNA ploidy level in 5033 individuals from 100 populations spread over the entire Eastern Alpine distribution area of S. carniolicus. Descriptors of microhabitats as well as spatial data were recorded in the field, and analysed with a mixed-effects ANOVA.

          Key Results

          Extensive variation in DNA ploidy levels (2 x, 3 x, 4 x, 5 x, 6 x, 7 x, 8 x, 9 x) was detected. Of the main cytotypes, diploids and hexaploids were widespread and had strongly overlapping distributions resulting in the frequent occurrence of cytotype mixtures (half of the investigated populations), whereas tetraploids were disjunctly distributed and occurred in the south-west and the east of the species' distribution area. In spite of the frequent co-occurrence of cytotypes, only 1 % of the samples belonged to secondary cytotypes (3 x, 5 x, 7 x, 8 x, 9 x). Diploids, tetraploids and hexaploids were altitudinally segregated, but with broad overlap. Similarly, highly significant differences in vegetation and rock cover as well as microhabitat exposure were found between the main cytotypes.

          Conclusions

          Senecio carniolicus shows a remarkable diversity of cytotypes. The distribution of the three main cytotypes (2 x, 4 x, 6 x) has been shaped by Pleistocene glaciations to different extents. Whereas tetraploids are nearly entirely restricted to refugia, hexaploids colonized areas that were extensively glaciated. Diploid and hexaploid individuals often co-occur in mixed populations, where they are spatially and ecologically segregated at both the meso-scale (altitudinal differentiation, exposure of the growing site) and the micro-scale (cover of vegetation and bare rock). With regard to the ecological parameters investigated, the tetraploid cytotype occupies an intermediate position. The rareness of secondary cytotypes suggests the presence of strong pre- or post-zygotic mating barriers.

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          Most cited references63

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          R: a language and environment for statistical computing

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            Genome evolution in polyploids.

            J Wendel (2000)
            Polyploidy is a prominent process in plants and has been significant in the evolutionary history of vertebrates and other eukaryotes. In plants, interdisciplinary approaches combining phylogenetic and molecular genetic perspectives have enhanced our awareness of the myriad genetic interactions made possible by polyploidy. Here, processes and mechanisms of gene and genome evolution in polyploids are reviewed. Genes duplicated by polyploidy may retain their original or similar function, undergo diversification in protein function or regulation, or one copy may become silenced through mutational or epigenetic means. Duplicated genes also may interact through inter-locus recombination, gene conversion, or concerted evolution. Recent experiments have illuminated important processes in polyploids that operate above the organizational level of duplicated genes. These include inter-genomic chromosomal exchanges, saltational, non-Mendelian genomic evolution in nascent polyploids, inter-genomic invasion, and cytonuclear stabilization. Notwithstanding many recent insights, much remains to be learned about many aspects of polyploid evolution, including: the role of transposable elements in structural and regulatory gene evolution; processes and significance of epigenetic silencing; underlying controls of chromosome pairing; mechanisms and functional significance of rapid genome changes; cytonuclear accommodation; and coordination of regulatory factors contributed by two, sometimes divergent progenitor genomes. Continued application of molecular genetic approaches to questions of polyploid genome evolution holds promise for producing lasting insight into processes by which novel genotypes are generated and ultimately into how polyploidy facilitates evolution and adaptation.
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              Molecular evidence for glacial refugia of mountain plants in the European Alps.

              Many mountain ranges have been strongly glaciated during the Quaternary ice ages, and the locations of glacial refugia of mountain plants have been debated for a long time. A series of detailed molecular studies, investigating intraspecific genetic variation of mountain plants in the European Alps, now allows for a first synopsis. A comparison of the phylogeographic patterns with geological and palaeoenvironmental data demonstrates that glacial refugia were located along the southwestern, southern, eastern and northern border of the Alps. Additional glacial refugia were present in central Alpine areas, where high-elevation plants survived the last glaciation on ice-free mountain tops. The observed intraspecific phylogeographies suggest general patterns of glacial survival, which conform to well-known centres of Alpine species diversity and endemism. This implies that evolutionary or biogeographic processes induced by climatic fluctuations act on gene and species diversity in a similar way.
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                Author and article information

                Journal
                Ann Bot
                annbot
                annbot
                Annals of Botany
                Oxford University Press
                0305-7364
                1095-8290
                December 2010
                29 September 2010
                29 September 2010
                : 106
                : 6
                : 967-977
                Affiliations
                [1 ]Department of Biogeography and Botanical Garden, University of Vienna, Rennweg 14, Vienna 1030, Austria
                [2 ]Institute of Botany, Academy of Sciences of the Czech Republic, Průhonice 1, CZ-252 43, Czech Republic
                [3 ]Department of Botany, Faculty of Science, Charles University in Prague, Benátská 2, Prague, CZ-128 01, Czech Republic
                [4 ]Systematic Botany and Mycology, Ludwig-Maximilians-University Munich, Menzingerstrasse 61, D-80638 Munich, Germany
                [5 ]Vienna Institute for Nature Conservation & Analyses, Giessergasse 6/7, Vienna 1090, Austria
                [6 ]Department of Conservation Biology, Vegetation Ecology and Landscape Ecology, University of Vienna, Rennweg 14, Vienna 1030, Austria
                [7 ]Department of Systematics, Palynology and Geobotany, Institute of Botany, University of Innsbruck, Sternwartestrasse 15, 6020 Innsbruck, Austria
                Author notes
                [* ]For correspondence. E-mail Karl.Huelber@ 123456univie.ac.at
                Article
                mcq192
                10.1093/aob/mcq192
                2990664
                20880930
                7256810d-e573-40d4-8708-3ccfb6170e3b
                © The Author 2010. Published by Oxford University Press on behalf of the Annals of Botany Company.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License ( http://creativecommons.org/licenses/by-nc/2.5), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 14 July 2010
                : 27 July 2010
                : 24 August 2010
                Categories
                Original Articles

                Plant science & Botany
                contact zones,eastern alps,refugia,cytotype mixture,polyploidy,senecio carniolicus,flow cytometry,ploidy level,habitat segregation

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