scholarly article | Q13442814 |
P356 | DOI | 10.1111/J.1095-8312.2004.00337.X |
P2093 | author name string | A. K. BRYSTING | |
A.-C. SCHEEN | |||
C. BROCHMANN | |||
H. H. GRUNDT | |||
I. G. ALSOS | |||
L. BORGEN | |||
R. ELVEN | |||
P433 | issue | 4 | |
P921 | main subject | polyploidy | Q213410 |
P304 | page(s) | 521-536 | |
P577 | publication date | 2004-08-09 | |
P1433 | published in | Biological Journal of the Linnean Society | Q2653025 |
P1476 | title | Polyploidy in arctic plants | |
P478 | volume | 82 |
Q46606470 | A high frequency of allopolyploid speciation in the gymnospermous genus Ephedra and its possible association with some biological and ecological features. |
Q35151597 | A synergism between adaptive effects and evolvability drives whole genome duplication to fixation |
Q42083279 | A world-wide perspective on crucifer speciation and evolution: phylogenetics, biogeography and trait evolution in tribe Arabideae |
Q111742507 | Adaptive responses drive the success of polyploid yellowcresses (Rorippa, Brassicaceae) in the Hengduan Mountains, a temperate biodiversity hotspot |
Q33661685 | Agronomic Trait Variations and Ploidy Differentiation of Kiwiberries in Northwest China: Implication for Breeding |
Q47246215 | Allopolyploid origin of highly invasive Centaurea stoebe s.l. (Asteraceae). |
Q31130676 | Amplified fragment length polymorphisms and sequence data in the phylogenetic analysis of polyploids: multiple origins of Veronica cymbalaria (Plantaginaceae). |
Q51615961 | An Andean radiation: polyploidy in the tree genus Polylepis (Rosaceae, Sanguisorbeae). |
Q30890746 | Biological invasions, climate change and genomics |
Q104736947 | Breeding system of diploid sexuals within the Ranunculus auricomus complex and its role in a geographical parthenogenesis scenario |
Q46403850 | Chasing ghosts: allopolyploid origin of Oxyria sinensis (Polygonaceae) from its only diploid congener and an unknown ancestor |
Q33563010 | Comparative molecular cytogenetic characterization of seven Deschampsia (Poaceae) species. |
Q35546424 | Conditions in home and transplant soils have differential effects on the performance of diploid and allotetraploid anthericum species |
Q28818377 | Cryptic diversity, geographical endemism and allopolyploidy in NE Pacific seaweeds |
Q100714890 | Cryptic genetic variability in Swainsona sericea (A. Lee) H. Eichler (Fabaceae): lessons for restoration |
Q92406454 | Cytogeography and chromosomal variation of the endemic East Asian herb Lycoris radiata |
Q37518771 | De novo transcriptome assembly, development of EST-SSR markers and population genetic analyses for the desert biomass willow, Salix psammophila |
Q46309136 | Disparity, diversity, and duplications in the Caryophyllales |
Q41043925 | Distribution, karyomorphology, and morphology of Aspidistra subrotata (Asparagaceae) at different ploidy levels in limestone areas of Asia |
Q37218198 | Divergence in Eco-Physiological Responses to Drought Mirrors the Distinct Distribution of Chamerion angustifolium Cytotypes in the Himalaya-Hengduan Mountains Region |
Q46439984 | Do floral and niche shifts favour the establishment and persistence of newly arisen polyploids? A case study in an Alpine primrose. |
Q56411426 | Do hybrid-origin polyploid amphibians occupy transgressive or intermediate ecological niches compared to their diploid ancestors? |
Q33649414 | Does polyploidy facilitate long-distance dispersal? |
Q100714897 | Ecological genetics of the wind-pollinated, tetraploid, Allocasuarina emuina L. Johnson (Casuarinaceae) from southeast Queensland reveals montane refugia for coastal heath during the last interglacial |
Q36239798 | Ecological range shift in the polyploid members of the South American genus Fosterella (Bromeliaceae). |
Q33808778 | Ecological studies of polyploidy in the 100 years following its discovery |
Q45864607 | Effect of phosphorus availability on the selection of species with different ploidy levels and genome sizes in a long-term grassland fertilization experiment |
Q38607379 | Endopolyploidy as a potential driver of animal ecology and evolution |
Q31043113 | Environmental aridity is associated with cytotype segregation and polyploidy occurrence in Brachypodium distachyon (Poaceae). |
Q35166887 | Evidence for shared broad-scale climatic niches of diploid and polyploid plants |
Q36186254 | Evolution in African tropical trees displaying ploidy-habitat association: The genus Afzelia (Leguminosae). |
Q47294916 | Evolution of biogeographic patterns, ploidy levels, and breeding systems in a diploid-polyploid species complex of Primula |
Q28603233 | Flow cytometry, microsatellites and niche models reveal the origins and geographical structure of Alnus glutinosa populations in Europe |
Q43297086 | Frozen ploidies: a phylogeographical analysis of the Leucanthemopsis alpina polyploid complex (Asteraceae, Anthemideae) |
Q34839318 | Genetic roadmap of the Arctic: plant dispersal highways, traffic barriers and capitals of diversity. |
Q110951054 | Genome size variation in Deschampsia cespitosa sensu lato (Poaceae) in Eurasia |
Q38751676 | Genome-wide analysis of the HD-ZIP IV transcription factor family in Gossypium arboreum and GaHDG11 involved in osmotic tolerance in transgenic Arabidopsis |
Q35586836 | Genomics in a changing arctic: critical questions await the molecular ecologist |
Q35193783 | Genomics of homoploid hybrid speciation: diversity and transcriptional activity of long terminal repeat retrotransposons in hybrid sunflowers |
Q36192925 | Geographic Variation in Festuca rubra L. Ploidy Levels and Systemic Fungal Endophyte Frequencies. |
Q111629061 | Geographical distribution of cytotypes in the Chrysanthemum indicum complex as evidenced by ploidy level and genome-size variation |
Q111629321 | Geographical distribution of cytotypes in theChrysanthemum indicumcomplex as evidenced by ploidy level and genome-size variation |
Q47288416 | Glacial in situ survival in the Western Alps and polytopic autopolyploidy in Biscutella laevigata L. (Brassicaceae). |
Q35121351 | High mountain origin, phylogenetics, evolution, and niche conservatism of arctic lineages in the hemiparasitic genus Pedicularis (Orobanchaceae). |
Q91942031 | Historical biogeography of the fern genus Polystichum (Dryopteridaceae) in Austral South America |
Q110697261 | Homoploid hybrids, allopolyploids, and high ploidy levels characterize the evolutionary history of a western North American quillwort (Isoëtes) complex |
Q46298198 | How much do we know about the frequency of hybridisation and polyploidy in the Mediterranean region? |
Q48266162 | How much of the invader's genetic variability can slip between our fingers? A case study of secondary dispersal of Poa annua on King George Island (Antarctica). |
Q29615012 | Hybrid speciation |
Q34483916 | Hybridisation and genetic diversity in introduced Mimulus (Phrymaceae). |
Q46738905 | Hybridization and reproductive isolation between diploid Erythronium mesochoreum and its tetraploid congener E. albidum (Liliaceae). |
Q50792223 | Hybridization, polyploidy, and the evolution of sexual systems in Mercurialis (Euphorbiaceae). |
Q34549657 | Hybridization, speciation and novelty |
Q33219929 | Impact of ice ages on circumpolar molecular diversity: insights from an ecological key species |
Q54716946 | In situ hybridization with genomic and rDNA probes reveals complex origins for polyploid New Zealand species ofPlantago(Plantaginaceae) |
Q111629490 | Increasing phylogenetic support for explosively radiating taxa: The promise of high-throughput sequencing for Oxytropis (Fabaceae) |
Q28651519 | Integrating environmental, molecular, and morphological data to unravel an ice-age radiation of arctic-alpine Campanula in western North America |
Q38404852 | Karyotypic changes through dysploidy persist longer over evolutionary time than polyploid changes |
Q104581391 | Maintenance of Species Differences in Closely Related Tetraploid Parasitic Euphrasia (Orobanchaceae) on an Isolated Island |
Q28727664 | Minority cytotypes in European populations of the Gymnadenia conopsea complex (Orchidaceae) greatly increase intraspecific and intrapopulation diversity |
Q35008419 | Miocene-Pliocene speciation, introgression, and migration of Patis and Ptilagrostis (Poaceae: Stipeae). |
Q24647639 | Molecular mechanisms of polyploidy and hybrid vigor |
Q30664388 | Molecular phylogeny of Koenigia L. (Polygonaceae: Persicarieae): implications for classification, character evolution and biogeography |
Q36049393 | Northern glacial refugia and altitudinal niche divergence shape genome-wide differentiation in the emerging plant model Arabidopsis arenosa |
Q33298665 | Nuclear vs. plastid data: complex Pleistocene history of a circumpolar key species. |
Q46659193 | On the relative abundance of autopolyploids and allopolyploids |
Q45040529 | Parallel evolutionary patterns in multiple lineages of arctic Artemisia L. (Asteraceae). |
Q36072699 | Patterns of abiotic niche shifts in allopolyploids relative to their progenitors |
Q91907678 | Pervasive population genomic consequences of genome duplication in Arabidopsis arenosa |
Q113676620 | Pioneering polyploids: the impact of whole-genome duplication on biome shifting in New Zealand Coprosma (Rubiaceae) and Veronica (Plantaginaceae) |
Q28754782 | Plants with double genomes might have had a better chance to survive the Cretaceous-Tertiary extinction event |
Q33205385 | Polyploid origins in a circumpolar complex in Draba (Brassicaceae) inferred from cloned nuclear DNA sequences and fingerprints |
Q34573988 | Polyploidy and microsatellite variation in the relict tree Prunus lusitanica L.: how effective are refugia in preserving genotypic diversity of clonal taxa? |
Q28657583 | Polyploidy and novelty: Gottlieb's legacy |
Q36999861 | Polyploidy can Confer Superiority to West African Acacia senegal (L.) Willd. Trees |
Q24657696 | Polyploidy in the olive complex (Olea europaea): evidence from flow cytometry and nuclear microsatellite analyses |
Q58495751 | Population genetic structure and conservation of the Azorean tree Prunus azorica (Rosaceae) |
Q64067237 | Postglacial colonization history reflects in the genetic structure of natural populations of in Europe |
Q90055857 | Preferential gene retention increases the robustness of cold regulation in Brassicaceae and other plants after polyploidization |
Q56066500 | Recent autopolyploidization in a naturalized population of Mimulus guttatus (Phrymaceae) |
Q48072291 | Reciprocal Pleistocene origin and postglacial range formation of an allopolyploid and its sympatric ancestors (Androsace adfinis group, Primulaceae). |
Q92162729 | Relaxed purifying selection in autopolyploids drives transposable element over-accumulation which provides variants for local adaptation |
Q46656013 | Revisiting the evolutionary events in Allium subgenus Cyathophora (Amaryllidaceae): Insights into the effect of the Hengduan Mountains Region (HMR) uplift and Quaternary climatic fluctuations to the environmental changes in the Qinghai-Tibet Plateau |
Q34097437 | Secondary metabolite profile in induced tetraploids of wild Solanum commersonii Dun. |
Q34609066 | Shift in cytotype frequency and niche space in the invasive plant Centaurea maculosa |
Q35084696 | Should I stay or should I go: biogeographic and evolutionary history of a polyploid complex (Chrysanthemum indicum complex) in response to Pleistocene climate change in China |
Q52616265 | Snapshot of DNA methylation changes associated with hybridization in Xenopus. |
Q35918241 | Spatial Genetic Structure of the Abundant and Widespread Peatmoss Sphagnum magellanicum Brid |
Q28657578 | Tangled up in two: a burst of genome duplications at the end of the Cretaceous and the consequences for plant evolution |
Q34520067 | Taxonomy and Biogeography of Apomixis in Angiosperms and Associated Biodiversity Characteristics |
Q38095683 | Temperature-size relations from the cellular-genomic perspective |
Q36245420 | Testing the Efficacy of DNA Barcodes for Identifying the Vascular Plants of Canada |
Q57061479 | Tetraploids do not form cushions: association of ploidy level, growth form and ecology in the High Arctic Saxifraga oppositifolia L. s. lat. (Saxifragaceae) in Svalbard |
Q36263909 | The Evolution of Vicia ramuliflora (Fabaceae) at Tetraploid and Diploid Levels Revealed with FISH and RAPD |
Q22122019 | The advantages and disadvantages of being polyploid |
Q38218016 | The causes and molecular consequences of polyploidy in flowering plants |
Q36546564 | The complex causality of geographical parthenogenesis |
Q62659224 | The global biogeography of polyploid plants |
Q28741287 | The more the better? The role of polyploidy in facilitating plant invasions |
Q35560368 | The origin of unique diversity in deglaciated areas: traces of Pleistocene processes in north-European endemics from the Galium pusillum polyploid complex (Rubiaceae). |
Q41918920 | The shock of being united and symphiliosis. Another lesson from plants? |
Q43806048 | Tracking the evolutionary history of polyploidy in Fragaria L. (strawberry): new insights from phylogenetic analyses of low-copy nuclear genes. |
Q48655251 | Two reproductively isolated cytotypes and a swarm of highly inbred, disconnected populations: a glimpse into Salicornia's evolutionary history and challenging taxonomy |
Q58700297 | Unscrambling phylogenetic effects and ecological determinants of chromosome number in major angiosperm clades |
Q28740913 | Unstable transcripts in Arabidopsis allotetraploids are associated with nonadditive gene expression in response to abiotic and biotic stresses |
Q33287371 | Untangling complex histories of genome mergings in high polyploids |
Q38952360 | What does the geography of parthenogenesis teach us about sex? |
Q34465043 | Widespread triploidy in Western North American aspen (Populus tremuloides) |
Q53383866 | microRNAs contribute to enhanced salt adaptation of the autopolyploid Hordeum bulbosum compared with its diploid ancestor. |
Q36199864 | rDNA Loci Evolution in the Genus Glechoma (Lamiaceae). |
Q22065707 | ‘Why polyploidy is rarer in animals than in plants’: myths and mechanisms |
Search more.