So Closely Related and Yet So Different: Strong Contrasts Between the Evolutionary Histories of Species of the Cardamine pratensis Polyploid Complex in Central Europe
Status PubMed-not-MEDLINE Jazyk angličtina Země Švýcarsko Médium electronic-ecollection
Typ dokumentu časopisecké články
PubMed
33391302
PubMed Central
PMC7775393
DOI
10.3389/fpls.2020.588856
Knihovny.cz E-zdroje
- Klíčová slova
- Brassicaceae, environmental niche, genome size, hybridization, microsatellites, phylogeography, polyploidy, target enrichment,
- Publikační typ
- časopisecké články MeSH
Recurrent polyploid formation and weak reproductive barriers between independent polyploid lineages generate intricate species complexes with high diversity and reticulate evolutionary history. Uncovering the evolutionary processes that formed their present-day cytotypic and genetic structure is a challenging task. We studied the species complex of Cardamine pratensis, composed of diploid endemics in the European Mediterranean and diploid-polyploid lineages more widely distributed across Europe, focusing on the poorly understood variation in Central Europe. To elucidate the evolution of Central European populations we analyzed ploidy level and genome size variation, genetic patterns inferred from microsatellite markers and target enrichment of low-copy nuclear genes (Hyb-Seq), and environmental niche differentiation. We observed almost continuous variation in chromosome numbers and genome size in C. pratensis s.str., which is caused by the co-occurrence of euploid and dysploid cytotypes, along with aneuploids, and is likely accompanied by inter-cytotype mating. We inferred that the polyploid cytotypes of C. pratensis s.str. are both of single and multiple, spatially and temporally recurrent origins. The tetraploid Cardamine majovskyi evolved at least twice in different regions by autopolyploidy from diploid Cardamine matthioli. The extensive genome size and genetic variation of Cardamine rivularis reflects differentiation induced by the geographic isolation of disjunct populations, establishment of triploids of different origins, and hybridization with sympatric C. matthioli. Geographically structured genetic lineages identified in the species under study, which are also ecologically divergent, are interpreted as descendants from different source populations in multiple glacial refugia. The postglacial range expansion was accompanied by substantial genetic admixture between the lineages of C. pratensis s.str., which is reflected by diffuse borders in their contact zones. In conclusion, we identified an interplay of diverse processes that have driven the evolution of the species studied, including allopatric and ecological divergence, hybridization, multiple polyploid origins, and genetic reshuffling caused by Pleistocene climate-induced range dynamics.
Botanical Garden Pavol Jozef Šafárik University Košice Slovakia
Central European Institute of Technology Masaryk University Brno Czechia
Department of Botany Faculty of Science Charles University Prague Czechia
Department of Experimental Biology Faculty of Science Masaryk University Brno Czechia
National Centre for Biomolecular Research Faculty of Science Masaryk University Brno Czechia
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Ančev M. (2006). Polyploidy and hybridization in Bulgarian Brassicaceae (Cruciferae): distribution and evolutionary role.
Ančev M., Yurukova-Grancharova P., Ignatova P., Goranova V., Stoyanov S., Yankova-Tsvetkova E., et al. (2013).
Anderson M. J. (2006). Distance-based tests for homogeneity of multivariate dispersions. PubMed DOI
Arrigo N., de La Harpe M., Litsios G., Zozomová-Lihová J., Španiel S., Marhold K., et al. (2016). Is hybridization driving the evolution of climatic niche in PubMed DOI
Baduel P., Bray S., Vallejo-Marin M., Kolář F., Yant L. (2018). The “Polyploid Hop”: shifting challenges and opportunities over the evolutionary lifespan of genome duplications. DOI
Baer K. C., Maron J. L. (2019). Declining demographic performance and dispersal limitation influence the geographic distribution of the perennial forb DOI
Bankevich A., Nurk S., Antipov D., Gurevich A. A., Dvorkin M., Kulikov A. S., et al. (2012). SPAdes: a new genome assembly algorithm and its applications to single-cell sequencing. PubMed DOI PMC
Bardy K. E., Albach D. C., Schneeweiss G. M., Fischer M. A., Schönswetter P. (2010). Disentangling phylogeography, polyploid evolution and taxonomy of a woodland herb ( PubMed DOI PMC
Bastkowski S., Mapleson D., Spillner A., Wu T., Balvociute M., Moulton V. (2018). SPECTRE: a suite of phylogenetic tools for reticulate evolution. PubMed DOI PMC
Bennetzen J. L., Ma J., Devos K. M. (2005). Mechanisms of recent genome size variation in flowering plants. PubMed DOI PMC
Birks H. J. B., Willis K. J. (2008). Alpines, trees, and refugia in Europe. DOI
Bolger A. M., Lohse M., Usadel B. (2014). Trimmomatic: a flexible trimmer for Illumina sequence data. PubMed DOI PMC
Borowiec M. L. (2016). AMAS: a fast tool for alignment manipulation and computing of summary statistics. PubMed DOI PMC
Brandrud M. K., Baar J., Lorenzo M. T., Athanasiadis A., Bateman R. M., Chase M. W., et al. (2020). Phylogenomic relationships of diploids and the origins of allotetraploids in PubMed DOI PMC
Brukhin V., Osadtchiy J. V., Florez-Rueda A. M., Smetanin D., Bakin E., Nobre M. S., et al. (2019). The PubMed DOI PMC
Bruvo R., Michiels N. K., D’Souza T. G., Schulenburg H. (2004). A simple method for the calculation of microsatellite genotype distances irrespective of ploidy level. PubMed DOI
Carter K. A., Liston A., Bassil N. V., Alice L. A., Bushakra J. M., Sutherland B. L., et al. (2019). Target capture sequencing unravels PubMed DOI PMC
Castro M., Loureiro J., Serrano M., Tavares D., Husband B. C., Siopa C., et al. (2019). Mosaic distribution of cytotypes in a mixed-ploidy plant species, DOI
Chernomor O., von Haeseler A., Minh B. Q. (2016). Terrace aware data structure for phylogenomic inference from supermatrices. PubMed DOI PMC
Clark L. V., Jasieniuk M. (2011). POLYSAT: an R package for polyploid microsatellite analysis. PubMed DOI
Coyne J. A., Orr H. A. (2004).
Dauphin B., Grant J. R., Farrar D. R., Rothfels C. J. (2018). Rapid allopolyploid radiation of moonwort ferns ( PubMed DOI
Dersch G. (1969). Über das Vorkommen von diploidem Wiesenschaumkraut (
Doležel J., Greilhuber J., Suda J. (2007a). Estimation of nuclear DNA content in plants using flow cytometry. PubMed DOI
Doležel J., Greilhuber J., Suda J. (2007b). “Flow cytometry with plants: an overview,” in DOI
Doležel J., Sgorbati S., Lucretti S. (1992). Comparison of three DNA fluorochromes for flow cytometric estimation of nuclear DNA content in plants. DOI
Dormann C. F., Elith J., Bacher S., Buchmann C., Carl G., Carré G., et al. (2013). Collinearity: a review of methods to deal with it and a simulation study evaluating their performance. DOI
Doyle J. J., Doyle J. L., Brown A. H., Grace J. P. (1990). Multiple origins of polyploids in the PubMed DOI PMC
Dray S., Dufour A. B. (2007). The ade4 package: implementing the duality diagram for ecologists. DOI
Dufresne F., Stift M., Vergilino R., Mable B. K. (2014). Recent progress and challenges in population genetics of polyploid organisms: an overview of current state-of-the-art molecular and statistical tools. PubMed DOI
Durović S., Schönswetter P., Niketić M., Tomović G., Frajman B. (2017). Disentangling relationships among the members of the DOI
Ehrich D. (2006). AFLPdat: a collection of R functions for convenient handling of AFLP data. DOI
Esselink G. D., Nybom H., Vosman B. (2004). Assignment of allelic configuration in polyploids using the MAC-PR (microsatellite DNA allele counting—peak ratios) method. PubMed DOI
Evanno G., Regnaut S., Goudet J. (2005). Detecting the number of clusters of individuals using the software STRUCTURE: a simulation study. PubMed DOI
Excoffier L., Smouse P. E., Quattro J. M. (1992). Analysis of molecular variance inferred from metric distances among DNA haplotypes: application to human mitochondrial DNA restriction data. PubMed PMC
Feulner M., Weig A., Voss T., Schott L. F., Aas G. (2019). Central European polyploids of DOI
Fick S. E., Hijmans R. J. (2017). WorldClim 2: new 1-km spatial resolution climate surfaces for global land areas. DOI
Frajman B., Rešetnik I., Niketić M., Ehrendorfer F., Schönswetter P. (2016). Patterns of rapid diversification in heteroploid PubMed DOI PMC
Franzke A., Hurka H. (2000). Molecular systematics and biogeography of the DOI
Friedman J., Hastie T., Tibshirani R. (2010). Regularization paths for generalized linear models via coordinate descent. PubMed DOI PMC
Gómez A., Lunt D. H. (2007). “Refugia within Refugia: Patterns of Phylogeographic Concordance in the Iberian Peninsula,” in DOI
Grabherr M. G., Haas B. J., Yassour M., Levin J. Z., Thompson D. A., Amit I., et al. (2011). Full-length transcriptome assembly from RNA-Seq data without a reference genome. PubMed DOI PMC
Greilhuber J., Dolezel J., Lysák M. A., Bennett M. D. (2005). The origin, evolution and proposed stabilization of the terms ‘genome size’ and ‘C-value’ to describe nuclear DNA contents. PubMed DOI PMC
Grünewald S., Spillner A., Bastkowski S., Bögershausen A., Moulton V. (2013). SuperQ: computing supernetworks from quartets. PubMed DOI
Hanušová K., Čertner M., Urfus T., Koutecký P., Košnar J., Rothfels C. J., et al. (2019). Widespread co-occurrence of multiple ploidy levels in fragile ferns ( PubMed DOI PMC
Heibl C. (2008).
Heuertz M., Carnevale S., Fineschi S., Sebastiani F., Hausman J. F., Paule L., et al. (2006). Chloroplast DNA phylogeography of European ashes, PubMed DOI
Heuertz M., Fineschi S., Anzidei M., Pastorelli R., Salvini D., Paule, et al. (2004). Chloroplast DNA variation and postglacial recolonization of common ash ( PubMed DOI
Hewitt G. (2000). The genetic legacy of the Quaternary ice ages. PubMed DOI
Hewitt G. M. (1999). Post-glacial re-colonization of European biota. DOI
Hewitt G. M. (2001). Speciation, hybrid zones and phylogeography—or seeing genes in space and time. PubMed
Hewitt G. M. (2004). Genetic consequences of climatic oscillations in the Quaternary. PubMed DOI PMC
Hodel R. G., Segovia-Salcedo M. C., Landis J. B., Crowl A. A., Sun M., Liu X., et al. (2016). The report of my death was an exaggeration: a review for researchers using microsatellites in the 21st century. PubMed DOI PMC
Hu Y. N., Zhao L., Buggs R. J., Zhang X. M., Li J., Wang N. (2019). Population structure of PubMed DOI PMC
Huang X. C., German D. A., Koch M. A. (2020). Temporal patterns of diversification in Brassicaceae demonstrate decoupling of rate shifts and mesopolyploidization events. PubMed DOI PMC
Hülber K., Sonnleitner M., Suda J., Krejčíková J., Schönswetter P., Schneeweiss G. M., et al. (2015). Ecological differentiation, lack of hybrids involving diploids, and asymmetric gene flow between polyploids in narrow contact zones of PubMed DOI PMC
Husband B. C. (2004). The role of triploid hybrids in the evolutionary dynamics of mixed-ploidy populations. DOI
Jakobsson M., Rosenberg N. A. (2007). CLUMPP: a cluster matching and permutation program for dealing with label switching and multimodality in analysis of population structure. PubMed DOI
Jankovská V., Pokorný P. (2008). Forest vegetation of the last full-glacial period in the Western Carpathians (Slovakia and Czech Republic).
Janská V., Jiménez-Alfaro B., Chytrý M., Divíšek J., Anenkhonov O., Korolyuk A., et al. (2017). Palaeodistribution modelling of European vegetation types at the Last Glacial Maximum using modern analogues from Siberia: Prospects and limitations. DOI
Johnson M. G., Gardner E. M., Liu Y., Medina R., Goffinet B., Shaw A. J., et al. (2016). HybPiper: Extracting coding sequence and introns for phylogenetics from high-throughput sequencing reads using target enrichment. PubMed DOI PMC
Junier T., Zdobnov E. M. (2010). The Newick utilities: high-throughput phylogenetic tree processing in the UNIX shell. PubMed DOI PMC
Kalyaanamoorthy S., Minh B. Q., Wong T. K., von Haeseler A., Jermiin L. S. (2017). ModelFinder: fast model selection for accurate phylogenetic estimates. PubMed DOI PMC
Kamvar Z. N., Brooks J. C., Grünwald N. J. (2015). Novel R tools for analysis of genome-wide population genetic data with emphasis on clonality. PubMed DOI PMC
Kamvar Z. N., Tabima J. F., Grünwald N. J. (2014). Poppr: an R package for genetic analysis of populations with clonal, partially clonal, and/or sexual reproduction. PubMed DOI PMC
Kates H. R., Johnson M. G., Gardner E. M., Zerega N. J., Wickett N. J. (2018). Allele phasing has minimal impact on phylogenetic reconstruction from targeted nuclear gene sequences in a case study of PubMed DOI
Katoh K., Toh H. (2008). Recent developments in the MAFFT multiple sequence alignment program. PubMed DOI
Kearse M., Moir R., Wilson A., Stones-Havas S., Cheung M., Sturrock S., et al. (2012). Geneious Basic: an integrated and extendable desktop software platform for the organization and analysis of sequence data. PubMed DOI PMC
Knaus B. J., Grünwald N. J. (2016). VcfR: a package to manipulate and visualize VCF format data in R. PubMed DOI
Knaus B. J., Grünwald N. J. (2017). VCFR: a package to manipulate and visualize variant call format data in R. PubMed DOI
Köhler C., Mittelsten Scheid O., Erilova A. (2010). The impact of the triploid block on the origin and evolution of polyploid plants. PubMed DOI
Kolář F., Čertner M., Suda J., Schönswetter P., Husband B. C. (2017). Mixed-ploidy species: progress and opportunities in polyploid research. PubMed DOI
Kolář F., Fuxová G., Záveská E., Nagano A. J., Hyklová L., Lučanová M., et al. (2016). Northern glacial refugia and altitudinal niche divergence shape genome-wide differentiation in the emerging plant model PubMed DOI
Kozlov A. M., Darriba D., Flouri T., Morel B., Stamatakis A. (2019). RAxML-NG: a fast, scalable and user-friendly tool for maximum likelihood phylogenetic inference. PubMed DOI PMC
Kučera J., Valko I., Marhold K. (2005). On-line database of the chromosome numbers of the genus
Kuhn M. (2019).
Landolt E. (1984). Über die Artengruppe der
Lawrence W. J. C. (1931). The chromosome constitution of DOI
Levin D. A. (1975). Minority cytotype exclusion in local plant populations. DOI
Li F.-W., Rushworth C. A., Beck J. B., Windham M. D. (2017). PubMed DOI PMC
Li H., Durbin R. (2009). Fast and accurate short read alignment with Burrows-Wheeler transform. PubMed DOI PMC
Li H., Handsaker B., Wysoker A., Fennell T., Ruan J., Homer N., et al. (2009). The Sequence Alignment/Map format and SAMtools. PubMed DOI PMC
Lihová J., Marhold K. (2003). Taxonomy and distribution of the
Lihová J., Marhold K. (2006). “Phylogenetic and diversity patterns in
Lihová J., Tribsch A., Marhold K. (2003). The DOI
Lihová J., Tribsch A., Stuessy T. F. (2004). DOI
Lövkvist B. (1956). The
Lynch M. (1990). The similarity index and DNA fingerprinting. PubMed DOI
Ma J. X., Li Y. N., Vogl C., Ehrendorfer F., Guo Y. P. (2010). Allopolyploid speciation and ongoing backcrossing between diploid progenitor and tetraploid progeny lineages in the PubMed DOI PMC
Magri D., Vendramin G. G., Comps B., Dupanloup I., Geburek T., Gömöry D., et al. (2006). A new scenario for the Quaternary history of European beech populations: palaeobotanical evidence and genetic consequences. PubMed DOI
Mandák B., Krak K., Vít P., Lomonosova M. N., Belyayev A., Habibi F., et al. (2018). Hybridization and polyploidization within the PubMed DOI
Mandáková T., Lysak M. A. (2018). Post-polyploid diploidization and diversification through dysploid changes. PubMed DOI
Mandáková T., Gloss A. D., Whiteman N. K., Lysak M. A. (2016). How diploidization turned a tetraploid into a pseudotriploid. PubMed DOI
Mandáková T., Kovařík A., Zozomová-Lihová J., Shimizu-Inatsugi R., Shimizu K. K., Mummenhoff K., et al. (2013). The more the merrier: recent hybridization and polyploidy in PubMed DOI PMC
Mandáková T., Zozomová-Lihová J., Kudoh H., Zhao Y., Lysak M. A., Marhold K. (2019). The story of promiscuous crucifers: origin and genome evolution of an invasive species, PubMed DOI PMC
Mantel N. (1967). The detection of disease clustering and a generalized regression approach. PubMed
Marhold K. (1992).
Marhold K. (1994a). Chromosome numbers of the genus
Marhold K. (1994b). Taxonomy of the genus
Marhold K. (1995).
Marhold K. (1996). Multivariate morphometric study of the DOI
Marhold K. (2000). Chromosome numbers of the
Marhold K., Záborský J. (1986). A new species of
Marhold K., Lihová J., Perný M., Grupe R., Neuffer B. (2002). Natural hybridization in DOI
Marhold K., Šlenker M., Zozomová-Lihová J. (2018). Polyploidy and hybridization in the Mediterranean and neighbouring areas towards the north: examples from the genus DOI
Martin M., Patterson M., Garg S., Fischer S., Pisanti N., Klau G. W., et al. (2016). WhatsHap: fast and accurate read-based phasing. DOI
Mason A. S., Pires J. C. (2015). Unreduced gametes: meiotic mishap or evolutionary mechanism? PubMed DOI
McCullagh P., Nelder J. A. (1989).
McKenna A., Hanna M., Banks E., Sivachenko A., Cibulskis K., Kernytsky A., et al. (2010). The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data. PubMed DOI PMC
Meirmans P. G., van Tienderen P. H. (2004). GENOTYPE and GENODIVE: two programs for the analysis of genetic diversity of asexual organisms. DOI
Meirmans P. G., Liu S., van Tienderen P. H. (2018). The analysis of polyploid genetic data. PubMed DOI
Melichárková A., Španiel S., Marhold K., Hurdu B. I., Drescher A., Zozomová-Lihová J. (2019). Diversification and independent polyploid origins in the disjunct species PubMed DOI
Monnahan P., Kolář F., Baduel P., Sailer C., Koch J., Horvath R., et al. (2019). Pervasive population genomic consequences of genome duplication in PubMed DOI
Nieto Feliner G. (2011). Southern European glacial refugia: a tale of tales. DOI
Nieto Feliner G. (2014). Patterns and processes in plant phylogeography in the Mediterranean Basin. DOI
Novikova P. Y., Hohmann N., Van de Peer Y. (2018). Polyploid PubMed DOI
Novikova P. Y., Tsuchimatsu T., Simon S., Nizhynska V., Voronin V., Burns R., et al. (2017). Genome sequencing reveals the origin of the allotetraploid PubMed DOI PMC
Obbard D. J., Harris S. A., Pannell J. R. (2006). Simple allelic-phenotype diversity and differentiation statistics for allopolyploids. PubMed DOI
Oksanen J., Blanchet F. G., Kindt R., Legendre P., Minchin P. R., O’Hara R. B., et al. (2019).
Pachschwöll C., Garcia P. E., Winkler M., Schneeweiss G. M., Schönswetter P. (2015). Polyploidisation and geographic differentiation drive diversification in a European high mountain plant group ( PubMed DOI PMC
Padilla-García N., Rojas-Andrés B. M., López-González N., Castro M., Castro S., Loureiro J., et al. (2018). The challenge of species delimitation in the diploid-polyploid complex PubMed DOI
Paradis E., Claude J., Strimmer K. (2004). APE: analyses of phylogenetics and evolution in R language. PubMed DOI
Parisod C., Holderegger R., Brochmann C. (2010). Evolutionary consequences of autopolyploidy. PubMed DOI
Paule J., Gregor T., Schmidt M., Gerstner E. M., Dersch G., Dressler S., et al. (2017). Chromosome numbers of the flora of Germany—A new online database of georeferenced chromosome counts and flow cytometric ploidy estimates. DOI
Pritchard J. K., Stephens M., Donnelly P. (2000). Inference of population structure using multilocus genotype data. PubMed PMC
R Core Team (2019).
Ramsey J., Schemske D. W. (1998). Pathways, mechanisms, and rates of polyploid formation in flowering plants. DOI
Rao C. R. (1964). The use and interpretation of principal component analysis in applied research.
Rešetnik I., Frajman B., Schönswetter P. (2016). Heteroploid PubMed DOI
Rojas-Andrés B. M., Padilla-García N., de Pedro M., López-González N., Delgado L., Albach D. C., et al. (2020). Environmental differences are correlated with the distribution pattern of cytotypes in PubMed DOI PMC
Ronikier M. (2011). Biogeography of high mountain plants in the Carpathians: an emerging phylogeographical perspective. DOI
Rosenberg N. A. (2004). DISTRUCT: a program for the graphical display of population structure. DOI
Saha S., Moorthi S., Pan H. L., Wu X., Wang J., Nadiga S., et al. (2010). The NCEP climate forecast system reanalysis. DOI
Sampson J. F., Byrne M. (2012). Genetic diversity and multiple origins of polyploid DOI
Schmickl R., Liston A., Zeisek V., Oberlander K., Weitemier K., Straub S. C., et al. (2016). Phylogenetic marker development for target enrichment from transcriptome and genome skim data: the pipeline and its application in southern African PubMed DOI
Schmickl R., Paule J., Klein J., Marhold K., Koch M. A. (2012). The evolutionary history of the PubMed DOI PMC
Schneider U., Becker A., Finger P., Meyer-Christoffer A., Ziese M., et al. (2014). GPCC’s new land surface precipitation climatology based on quality-controlled in situ data and its role in quantifying the global water cycle. DOI
Schönswetter P., Tribsch A. (2005). Vicariance and dispersal in the alpine perennial DOI
Schönswetter P., Suda J., Popp M., Weiss-Schneeweiss H., Brochmann C. (2007). Circumpolar phylogeography of PubMed DOI
Servick S., Visger C. J., Gitzendanner M. A., Soltis P. S., Soltis D. E. (2015). Population genetic variation, geographic structure, and multiple origins of autopolyploidy in PubMed DOI
Skokanová K., Šingliarová B., Kochjarová J., Paule J. (2019). Nuclear ITS and AFLPs provide surprising implications for the taxonomy of DOI
Slater G. S., Birney E. (2005). Automated generation of heuristics for biological sequence comparison. PubMed DOI PMC
Slovák M., Kučera J., Turis P., Zozomová-Lihová J. (2012). Multiple glacial refugia and postglacial colonization routes inferred for a woodland geophyte, DOI
Soltis D. E., Soltis P. S., Tate J. A. (2003). Advances in the study of polyploidy since plant speciation. DOI
Soltis D. E., Soltis P. S., Pires J. C., Kovařík A., Tate J. A., Mavrodiev E. (2004). Recent and recurrent polyploidy in DOI
Soltis D. E., Soltis P. S., Schemske D. W., Hancock J. F., Thompson J. N., Husband B. C., et al. (2007). Autopolyploidy in angiosperms: have we grossly underestimated the number of species? DOI
Soltis P. S., Soltis D. E. (2009). The role of hybridization in plant speciation. PubMed DOI
Soltis P. S., Liu X., Marchant D. B., Visger C. J., Soltis D. E. (2014). Polyploidy and novelty: Gottlieb’s legacy. PubMed DOI PMC
Sonnleitner M., Weis B., Flatscher R., García P. E., Suda J., Krejčíková J., et al. (2013). Parental ploidy strongly affects offspring fitness in heteroploid crosses among three cytotypes of autopolyploid PubMed DOI PMC
Španiel S., Marhold K., Zozomová-Lihová J. (2017). The polyploid DOI
Španiel S., Marhold K., Zozomová-Lihová J. (2019). Polyphyletic DOI
Španiel S., Marhold K., Filová B., Zozomová-Lihová J. (2011). Genetic and morphological variation in the diploid-polyploid DOI
Šrámková-Fuxová G., Záveská E., Kolář F., Lučanová M., Španiel S., Marhold K. (2017). Range-wide genetic structure of DOI
Stachurska-Swakoń A., Cieślak E., Ronikier M., Nowak J., Kaczmarczyk A. (2020). Genetic structure of DOI
Stewart J. R., Lister A. M., Barnes I., Dalén L. (2010). Refugia revisited: individualistic responses of species in space and time. PubMed DOI PMC
Stift M., Kolář F., Meirmans P. G. (2019). STRUCTURE is more robust than other clustering methods in simulated mixed-ploidy populations. PubMed DOI PMC
Sutherland B. L., Galloway L. F. (2017). Postzygotic isolation varies by ploidy level within a polyploid complex. PubMed DOI
Svenning J. C., Skov F. (2007). Could the tree diversity pattern in Europe be generated by postglacial dispersal limitation? PubMed DOI
Szpiech Z. A., Jakobsson M., Rosenberg N. A. (2008). ADZE: a rarefaction approach for counting alleles private to combinations of populations. PubMed DOI PMC
Temsch E. M., Greilhuber J., Krisai R. (2010). Genome size in liverworts.
Těšitel J., Malinová T., Štech M., Herbstová M. (2009). Variation in the
Tibshirani R. (1996). Regression shrinkage and selection via the lasso. DOI
Tomasello S., Karbstein K., Hodač L., Paetzold C., Hörandl E. (2020). Phylogenomics unravels Quaternary vicariance and allopatric speciation patterns in temperate-montane plant species: a case study on the PubMed DOI
Udall J. A., Long E., Ramaraj T., Conover J. L., Yuan D., Grover C. E., et al. (2019). The genome sequence of PubMed DOI PMC
Urbanska K. M., Hurka H., Landolt E., Neuffer B., Mummenhoff K. (1997). Hybridization and evolution in DOI
Urbanska-Worytkiewicz K., Landolt E. (1974). Biosystematics investigations in
Villaverde T., Pokorny L., Olsson S., Rincón-Barrado M., Johnson M. G., Gardner E. M., et al. (2018). Bridging the micro-and macroevolutionary levels in phylogenomics: Hyb-Seq solves relationships from populations to species and above. PubMed DOI
Weitemier K., Straub S. C., Cronn R. C., Fishbein M., Schmickl R., McDonnell A., et al. (2014). Hyb-Seq: Combining target enrichment and genome skimming for plant phylogenomics. PubMed DOI PMC
Wickham H. (2016).
Willner W., Di Pietro R., Bergmeier E. (2009). Phytogeographical evidence for post-glacial dispersal limitation of European beech forest species. DOI
Wos G., Mořkovská J., Bohutínská M., Šrámková G., Knotek A., Lučanová M., et al. (2019). Role of ploidy in colonization of alpine habitats in natural populations of PubMed DOI PMC
Zozomová-Lihová J., Krak K., Mandáková T., Shimizu K. K., Španiel S., Vít P., et al. (2014a). Multiple hybridization events in PubMed DOI PMC
Zozomová-Lihová J., Malánová-Krásná I., Vít P., Urfus T., Senko D., Svitok M., et al. (2015). Cytotype distribution patterns, ecological differentiation, and genetic structure in a diploid-tetraploid contact zone of PubMed DOI
Zozomová-Lihová J., Mandáková T., Kovaříková A., Mühlhausen A., Mummenhoff K., Lysak M. A., et al. (2014b). When fathers are instant losers: homogenization of rDNA loci in recently formed PubMed DOI