So Closely Related and Yet So Different: Strong Contrasts Between the Evolutionary Histories of Species of the Cardamine pratensis Polyploid Complex in Central Europe

. 2020 ; 11 () : 588856. [epub] 20201218

Status PubMed-not-MEDLINE Jazyk angličtina Země Švýcarsko Médium electronic-ecollection

Typ dokumentu časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/pmid33391302

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.

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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

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