| scholarly article | Q13442814 |
| P50 | author | David Mark Richardson | Q11256815 |
| Jan Suda | Q26713876 | ||
| Petr Pyšek | Q28028614 | ||
| Mariska te Beest | Q92348788 | ||
| Johannes J. Le Roux | Q37371338 | ||
| P2093 | author name string | Anne K Brysting | |
| Magdalena Kubesová | |||
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| Introduced plants of the invasive Solidago gigantea (Asteraceae) are larger and grow denser than conspecifics in the native range | Q55870803 | ||
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| Polyploid Incidence and Evolution | Q22065392 | ||
| Neopolyploidy in Flowering Plants | Q22065401 | ||
| PATHWAYS, MECHANISMS, AND RATES OF POLYPLOID FORMATION IN FLOWERING PLANTS | Q22065403 | ||
| Ploidy influences rarity and invasiveness in plants | Q22065697 | ||
| ‘Why polyploidy is rarer in animals than in plants’: myths and mechanisms | Q22065707 | ||
| Flow cytometry and GISH reveal mixed ploidy populations and Spartina nonaploids with genomes of S. alterniflora and S. maritima origin | Q22066080 | ||
| The frequency of polyploid speciation in vascular plants | Q22066293 | ||
| The advantages and disadvantages of being polyploid | Q22122019 | ||
| Molecular mechanisms of polyploidy and hybrid vigor | Q24647639 | ||
| Genetic and epigenetic mechanisms for gene expression and phenotypic variation in plant polyploids | Q24679271 | ||
| Coincidence, coevolution, or causation? DNA content, cell size, and the C-value enigma | Q28185889 | ||
| Polyploidy and genome evolution in plants | Q28238570 | ||
| The origin, evolution and proposed stabilization of the terms 'genome size' and 'C-value' to describe nuclear DNA contents | Q28298127 | ||
| Spread of Exotic Cordgrasses and Hybrids (Spartina sp.) in the Tidal Marshes of San Francisco Bay, California, USA | Q28314822 | ||
| A proposed unified framework for biological invasions | Q28342438 | ||
| The large genome constraint hypothesis: evolution, ecology and phenotype | Q28651140 | ||
| Genome size evolution in relation to leaf strategy and metabolic rates revisited | Q28749369 | ||
| Genome size scaling through phenotype space | Q28752265 | ||
| Plants with double genomes might have had a better chance to survive the Cretaceous-Tertiary extinction event | Q28754782 | ||
| Neopolyploidy and pathogen resistance | Q28755281 | ||
| Rates of evolution in seed plants: Net increase in diversity of chromosome numbers and species numbers through time | Q28775774 | ||
| The significance of responses of the genome to challenge | Q28913697 | ||
| The Biosystematics of Achlys | Q28952317 | ||
| Minority Cytotype Exclusion in Local Plant Populations | Q28954054 | ||
| Cytology and Cytogenetics as a Fundamental Taxonomic Resource for the 20th and 21st Centuries | Q28958932 | ||
| DNA Amounts in Two Samples of Angiosperm Weeds | Q57067710 | ||
| Recent and recurrent polyploidy in Tragopogon (Asteraceae): cytogenetic, genomic and genetic comparisons | Q58044795 | ||
| Seed size and plant strategy across the whole life cycle | Q58396352 | ||
| The production of hybrids with high ecological amplitude between exotic Spartina densiflora and native S. maritima in the Iberian Peninsula | Q58879955 | ||
| Patterns of hybridization and hybrid survival in the invasive alienFallopia complex(Polygonaceae) | Q59293106 | ||
| Ecological, morphological and allozymic differentiation between diploid and tetraploid knapweeds (Centaurea jacea) from a contact zone in the Belgian Ardennes | Q59293304 | ||
| Niche differentiation between diploid and hexaploid Aster amellus | Q60315002 | ||
| Cytogeography and chromosome evolution of subgenus Tridentatae of Artemisia (Asteraceae) | Q73284328 | ||
| Genomic change and gene silencing in polyploids | Q77219252 | ||
| Polyploidy: recurrent formation and genome evolution | Q78109192 | ||
| Selfish DNA is maladaptive: evidence from the plant Red List | Q79224478 | ||
| Transcriptome shock after interspecific hybridization in senecio is ameliorated by genome duplication | Q80141703 | ||
| Multiple spindles and cellularization during microsporogenesis in an artificially induced tetraploid accession of Brachiaria ruziziensis (Gramineae) | Q80559779 | ||
| Polyploidy: doubling up for evolutionary success | Q81554000 | ||
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| Effects of Polyploidy on Photosynthetic Rates, Photosynthetic Enzymes, Contents of DNA, Chlorophyll, and Sizes and Numbers of Photosynthetic Cells in the C(4) Dicot Atriplex confertifolia | Q83269103 | ||
| Focus on polyploidy | Q84087199 | ||
| Genome duplication and the evolution of physiological responses to water stress | Q84457158 | ||
| Genetic improvement of Egyptian henbane, Hyoscyamus muticus L. through induced tetraploidy | Q86759271 | ||
| Aneuploidy and inbreeding depression in random mating and self-fertilizing autotetraploid populations | Q86780049 | ||
| Variation for 2n pollen production in clones of Solanum phureja Juz. and Buk | Q86844797 | ||
| EVIDENCE FOR AUTOPOLYPLOIDY IN EPILOBIUM ANGUSTIFOLIUM (ONAGRACEAE) | Q88195980 | ||
| PLANT POLYPLOIDY AND POLLINATION: FLORAL TRAITS AND INSECT VISITS TO DIPLOID AND TETRAPLOID HEUCHERA GROSSULARIIFOLIA | Q88201138 | ||
| Comparative ecophysiology of the chromosome races in Viola adunca J.E. Smith | Q89573379 | ||
| Human Agency in Biological Invasions: Secondary Releases Foster Naturalisation and Population Expansion of Alien Plant Species | Q110985301 | ||
| Ploidy Level versus DNA Ploidy Level: An Appeal for Consistent Terminology | Q28960248 | ||
| Evolutionary consequences of autopolyploidy | Q29394621 | ||
| Stomatal size in fossil plants: evidence for polyploidy in majority of angiosperms | Q29547784 | ||
| The evolutionary significance of ancient genome duplications | Q29617105 | ||
| Naturalization and invasion of alien plants: concepts and definitions | Q30052190 | ||
| Outcrossing rate and inbreeding depression in the herbaceous autotetraploid, Campanula americana | Q30310765 | ||
| Demography of the invasive geophyte Oxalis pes-caprae across a Mediterranean island | Q30397111 | ||
| Genomic admixture increases fitness during a biological invasion | Q30451329 | ||
| Disentangling the role of environmental and human pressures on biological invasions across Europe | Q30495396 | ||
| Variation in DNA-ploidy Levels of Reynoutria Taxa in the Czech Republic | Q30601874 | ||
| Comparison of genetic diversity of the invasive weed Rubus alceifolius poir. (Rosaceae) in its native range and in areas of introduction, using amplified fragment length polymorphism (AFLP) markers. | Q30850963 | ||
| Ecological factors influencing tetraploid speciation in snow buttercups (Ranunculus Adoneus): niche differentiation and tetraploid establishment | Q31014998 | ||
| Untangling complex histories of genome mergings in high polyploids | Q33287371 | ||
| Genomic plasticity and the diversity of polyploid plants | Q33330809 | ||
| Plant origin and ploidy influence gene expression and life cycle characteristics in an invasive weed | Q33421093 | ||
| Distribution of flower morphs, ploidy level and sexual reproduction of the invasive weed Oxalis pes-caprae in the western area of the Mediterranean region | Q33576661 | ||
| Hybridization and sexual reproduction in the invasive alien Fallopia (Polygonaceae) complex in Belgium | Q33576757 | ||
| The making of a rapid plant invader: genetic diversity and differentiation in the native and invaded range of Senecio inaequidens | Q33696445 | ||
| Do invasive species show higher phenotypic plasticity than native species and, if so, is it adaptive? A meta-analysis | Q33818626 | ||
| Testing Darwin's naturalization hypothesis in the Azores | Q33820176 | ||
| Native perennial grasses show evolutionary response to Bromus tectorum (cheatgrass) invasion | Q33867315 | ||
| Altered gene expression and ecological divergence in sibling allopolyploids of Dactylorhiza (Orchidaceae) | Q33882312 | ||
| Ecological impacts of invasive alien plants: a meta-analysis of their effects on species, communities and ecosystems | Q33904581 | ||
| Hybridization as a stimulus for the evolution of invasiveness in plants? | Q33947000 | ||
| Chromosomal rearrangements and speciation | Q33951087 | ||
| The epigenetics of nucleolar dominance | Q34080527 | ||
| Stable epigenetic effects impact adaptation in allopolyploid orchids (Dactylorhiza: Orchidaceae) | Q34120946 | ||
| Understanding mechanisms of novel gene expression in polyploids | Q34180932 | ||
| Distribution and habitat segregation on different spatial scales among diploid, tetraploid and hexaploid cytotypes of Senecio carniolicus (Asteraceae) in the Eastern Alps | Q34344373 | ||
| Genes duplicated by polyploidy show unequal contributions to the transcriptome and organ-specific reciprocal silencing | Q34532390 | ||
| On the abundance of polyploids in flowering plants | Q34554901 | ||
| Genomewide nonadditive gene regulation in Arabidopsis allotetraploids | Q34587400 | ||
| Shift in cytotype frequency and niche space in the invasive plant Centaurea maculosa | Q34609066 | ||
| Cytotype distribution at a diploid-tetraploid contact zone in Chamerion (Epilobium) angustifolium (Onagraceae). | Q34630703 | ||
| The evolutionary consequences of polyploidy | Q34709080 | ||
| Evolutionary and ecological implications of genome size in the North American endemic sagebrushes and allies (Artemisia, Asteraceae) | Q56287642 | ||
| Trees and shrubs as invasive alien species - a global review | Q56744539 | ||
| Macroecology meets invasion ecology: linking the native distributions of Australian acacias to invasiveness | Q56744608 | ||
| Invasiveness in introduced Australian acacias: the role of species traits and genome size | Q56744619 | ||
| Predicting invasiveness of Australian acacias on the basis of their native climatic affinities, life history traits and human use | Q56744659 | ||
| The phenology of plant invasions: a community ecology perspective | Q56752474 | ||
| Polyploidy and invasion success: trait trade-offs in native and introduced cytotypes of two Asteraceae species | Q56764400 | ||
| Functional differences between native and alien species: a global-scale comparison | Q56765695 | ||
| Limits to the niche and range margins of alien species | Q56766785 | ||
| Evidence for climatic niche and biome shifts between native and novel ranges in plant species introduced to Australia | Q56767287 | ||
| Evidence for a combination of pre-adapted traits and rapid adaptive change in the invasive plant Centaurea stoebe | Q56767290 | ||
| How well do we understand the impacts of alien species on ecosystem services? A pan-European, cross-taxa assessment | Q56768110 | ||
| Invasibility or invasiveness? Effects of habitat, genotype, and their interaction on invasive Rhododendron ponticum populations | Q56768355 | ||
| Spreading to a limit: the time required for a neophyte to reach its maximum range | Q56768385 | ||
| The global invasion success of Central European plants is related to distribution characteristics in their native range and species traits | Q56770533 | ||
| Impact of invasive plants on the species richness, diversity and composition of invaded communities | Q56771690 | ||
| Seedling establishment of Asteraceae forbs along altitudinal gradients: a comparison of transplant experiments in the native and introduced ranges | Q56772122 | ||
| Mahonia invasions in different habitats: local adaptation or general-purpose genotypes? | Q56772420 | ||
| The distribution of range sizes of native and alien plants in four European countries and the effects of residence time | Q56772739 | ||
| Cytogeography ofSolidago gigantea(Asteraceae) and its invasive ploidy level | Q56773457 | ||
| Trait interactions help explain plant invasion success in the German flora | Q56773812 | ||
| Selection of preadapted populations allowed Senecio inaequidens to invade Central Europe | Q56774148 | ||
| The potential role of polyploidy and hybridisation in the further evolution of the highly invasive Fallopia taxa in Europe | Q56776804 | ||
| Predicting naturalization of southern African Iridaceae in other regions | Q56777881 | ||
| Explaining and predicting the success of invading species at different stages of invasion | Q56779890 | ||
| Polyploidy in invasive plant species of Singapore | Q56780579 | ||
| Local and regional assessments of the impacts of plant invaders on vegetation structure and soil properties of Mediterranean islands | Q56781069 | ||
| Life-history correlates of plant invasiveness at regional and continental scales | Q56782652 | ||
| Do vigour of introduced populations and escape from specialist herbivores contribute to invasiveness? | Q56784151 | ||
| Conifers as invasive aliens: a global survey and predictive framework | Q56785174 | ||
| Latitudinal trends in growth and phenology of the invasive alien plant Impatiens glandulifera (Balsaminaceae) | Q56785190 | ||
| Breeding systems of invasive alien plants in South Africa: does Baker's rule apply? | Q56785201 | ||
| Asexual populations of the invasive weed Oxalis pes-caprae are genetically variable | Q56894926 | ||
| Fifty years of invasion ecology - the legacy of Charles Elton | Q56922903 | ||
| Residence time and potential range: crucial considerations in modelling plant invasions | Q56922965 | ||
| What Attributes Make Some Plant Species More Invasive? | Q56923184 | ||
| Clone-specific differences in Phragmites australis: Effects of ploidy level and geographic origin | Q56947321 | ||
| Ploidy-specific interactions of three host plants with arbuscular mycorrhizal fungi: Does genome copy number matter? | Q57014920 | ||
| Applications of Flow Cytometry to Evolutionary and Population Biology | Q57014937 | ||
| The Biology of Invasive Alien Plants in Canada. 5. Polygonum cuspidatum Sieb. & Zucc. [= Fallopia japonica (Houtt.) Ronse Decr.] | Q57049513 | ||
| Polyploidy in arctic plants | Q57061530 | ||
| Genome downsizing in polyploid plants | Q57067661 | ||
| The adaptive value of remnant native plants in invaded communities: an example from the Great Basin. | Q45937514 | ||
| Evolution of genome size in pines (Pinus) and its life-history correlates: supertree analyses | Q46321351 | ||
| Differential accumulation of retroelements and diversification of NB-LRR disease resistance genes in duplicated regions following polyploidy in the ancestor of soybean. | Q46325461 | ||
| Polyploidy and ecological adaptation in wild yarrow | Q34880439 | ||
| Polyploidy and ecological transfiguration in Achillea | Q34880802 | ||
| Evolution and expression of homeologous loci in Tragopogon miscellus (Asteraceae), a recent and reciprocally formed allopolyploid | Q34898004 | ||
| Epigenetic phenomena and the evolution of plant allopolyploids | Q35582638 | ||
| Increased genetic variation and evolutionary potential drive the success of an invasive grass | Q35652763 | ||
| Novel patterns of gene expression in polyploid plants | Q36228503 | ||
| Jack of all trades, master of some? On the role of phenotypic plasticity in plant invasions | Q36567792 | ||
| Strong human association with plant invasion success for Trifolium introductions to New Zealand | Q36609181 | ||
| Evolution of duplicate gene expression in polyploid and hybrid plants | Q36701858 | ||
| Genome plasticity a key factor in the success of polyploid wheat under domestication | Q36864536 | ||
| Ecological factors influencing tetraploid establishment in snow buttercups (Ranunculus adoneus , Ranunculaceae): minority cytotype exclusion and barriers to triploid formation | Q39114698 | ||
| To succeed globally, disperse locally: effects of local pollen and seed dispersal on tetraploid establishment | Q39129972 | ||
| Polyploidy and habitat differentiation in Dactylis glomerata L. from Galicia (Spain). | Q39193867 | ||
| Latitudinal population differentiation in two species of Solidago (Asteraceae) introduced into Europe | Q39226612 | ||
| Nuclear volume control by nucleoskeletal DNA, selection for cell volume and cell growth rate, and the solution of the DNA C-value paradox | Q39791026 | ||
| Nuclear DNA content and minimum generation time in herbaceous plants | Q39907465 | ||
| Sensitivity of the invasive geophyte Oxalis pes-caprae to nutrient availability and competition | Q41884555 | ||
| Genome size reduction can trigger rapid phenotypic evolution in invasive plants | Q41907469 | ||
| The relationship between nuclear DNA content and leaf strategy in seed plants | Q42006778 | ||
| Evolution of polyploidy and the diversification of plant-pollinator interactions | Q42028171 | ||
| Plant polyploidy and host expansion in an insect herbivore. | Q42052339 | ||
| Chloroplast DNA diversity of Hieracium Pilosella (Asteraceae) introduced to New Zealand: reticulation, hybridization, and invasion | Q42604062 | ||
| Transcriptomic changes following recent natural hybridization and allopolyploidy in the salt marsh species Spartina x townsendii and Spartina anglica (Poaceae). | Q43995893 | ||
| Hybridization between invasive Spartina densiflora (Poaceae) and native S. foliosa in San Francisco Bay, California, USA. | Q44594939 | ||
| Correlated evolution of genome size and seed mass | Q44619898 | ||
| Reliable DNA ploidy determination in dehydrated tissues of vascular plants by DAPI flow cytometry--new prospects for plant research | Q44957192 | ||
| Plant polyploidy and insect/plant interactions | Q45716580 | ||
| Mitotic instability in resynthesized and natural polyploids of the genus Arabidopsis (Brassicaceae). | Q45772076 | ||
| P433 | issue | 1 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | polyploidy | Q213410 |
| plant invasion | Q106035592 | ||
| invasion facilitation | Q112111173 | ||
| invasion biology | Q42985020 | ||
| P6104 | maintained by WikiProject | WikiProject Invasion Biology | Q56241615 |
| P1104 | number of pages | 27 | |
| P304 | page(s) | 19-45 | |
| P577 | publication date | 2012-01-01 | |
| P1433 | published in | Annals of Botany | Q1821243 |
| P1476 | title | The more the better? The role of polyploidy in facilitating plant invasions | |
| P478 | volume | 109 |
| Q92098781 | A new biological species in the Mercurialis annua polyploid complex: functional divergence in inflorescence morphology and hybrid sterility |
| Q30619500 | A review of the allozyme data set for the Canarian endemic flora: causes of the high genetic diversity levels and implications for conservation |
| Q35151597 | A synergism between adaptive effects and evolvability drives whole genome duplication to fixation |
| Q55253963 | AFLP-based genetic diversity of wild orchardgrass germplasm collections from Central Asia and Western China, and the relation to environmental factors. |
| 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 |
| Q28654997 | Analysis of 41 plant genomes supports a wave of successful genome duplications in association with the Cretaceous-Paleogene boundary |
| Q35545535 | Assignment of homoeologs to parental genomes in allopolyploids for species tree inference, with an example from Fumaria (papaveraceae). |
| Q91639132 | Beyond Arabidopsis: Differential UV-B Response Mediated by UVR8 in Diverse Species |
| Q30990801 | Binucleation to breed new plant species adaptable to their environments. |
| Q56525146 | Biogeographic comparisons of herbivore attack, growth and impact of Japanese knotweed between Japan and France |
| Q48309713 | Biological invasion of oxeye daisy (Leucanthemum vulgare) in North America: Pre-adaptation, post-introduction evolution, or both? |
| Q30890746 | Biological invasions, climate change and genomics |
| Q56929404 | CHARACTERISTICS OF SUCCESSFUL ALIEN PLANTS |
| Q110531546 | Can enemy release explain the invasion success of the diploid Leucanthemum vulgare in North America? |
| Q96822305 | Can polyploidy confer invasive plants with a wider climatic tolerance? A test using Solidago canadensis |
| Q36560882 | Can resource costs of polyploidy provide an advantage to sex? |
| Q38548568 | Cancer quasispecies and stem-like adaptive aneuploidy |
| Q58627928 | Characterizing the allopolyploid species among the wild relatives of soybean: Utility of reduced representation genotyping methodologies |
| Q36643343 | Chromosome numbers in three species groups of freshwater flatworms increase with increasing latitude. |
| Q33680303 | Chromosome numbers of populations of three varieties of Bidens pilosa in Taiwan |
| Q44645885 | Chromosome numbers, characterization of chromosomal pairing during meiosis, origin and natural propagation in polyploid cytotypes (4x, 5x and 6x) of Agrimonia eupatoria L. (Rosaceae) in northwest Himalayas (India). |
| Q55397891 | Climatic differentiation in polyploid apomictic Ranunculus auricomus complex in Europe. |
| Q56484365 | Clonal structure and reduced diversity of the invasive alien plant Erigeron annuus in Lithuania |
| Q34416290 | Community impacts of Prosopis juliflora invasion: biogeographic and congeneric comparisons |
| Q89793272 | Competition among native and invasive Phragmites australis populations: An experimental test of the effects of invasion status, genome size, and ploidy level |
| Q90218933 | Competition of Parental Genomes in Plant Hybrids |
| Q51151780 | Competitive ability of Capsella species with different mating systems and ploidy levels. |
| Q37335870 | Conserved but Attenuated Parental Gene Expression in Allopolyploids: Constitutive Zinc Hyperaccumulation in the Allotetraploid Arabidopsis kamchatica. |
| Q35586918 | Contrasting growth phenology of native and invasive forest shrubs mediated by genome size |
| Q28818377 | Cryptic diversity, geographical endemism and allopolyploidy in NE Pacific seaweeds |
| Q92406454 | Cytogeography and chromosomal variation of the endemic East Asian herb Lycoris radiata |
| Q57014892 | Cytogeography of Oxalis pes-caprae in its native range: where are the pentaploids? |
| Q35863502 | Cytonuclear Coordination Is Not Immediate upon Allopolyploid Formation in Tragopogon miscellus (Asteraceae) Allopolyploids |
| Q37518771 | De novo transcriptome assembly, development of EST-SSR markers and population genetic analyses for the desert biomass willow, Salix psammophila |
| Q64061965 | Difference in reproductive mode rather than ploidy explains niche differentiation in sympatric sexual and apomictic populations of |
| Q48243622 | Differential content of secondary metabolites in diploid and tetraploid cytotypes of Siegesbeckia orientalis L. |
| Q26810452 | Disaggregating polyploidy, parental genome dosage and hybridity contributions to heterosis in Arabidopsis thaliana |
| 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. |
| Q56946586 | Do ploidy level and nuclear genome size and latitude of origin modify the expression of Phragmites australis traits and interactions with herbivores? |
| Q33649414 | Does polyploidy facilitate long-distance dispersal? |
| Q48540758 | Double trouble: taxonomy and definitions of polyploidy |
| Q33951897 | Drought tolerance and plasticity in the invasive knapweed Centaurea stoebe s.l. (Asteraceae): effect of populations stronger than those of cytotype and range |
| Q35866835 | Ecological differentiation of diploid and polyploid cytotypes of Senecio carniolicus sensu lato (Asteraceae) is stronger in areas of sympatry |
| Q89749749 | Ecological niche differences between two polyploid cytotypes of Saxifraga rosacea |
| 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 |
| Q56502024 | Ecophysiological plasticity and local differentiation help explain the invasion success ofTaraxacum officinale(dandelion) in South America |
| Q51161111 | Effect of Environmental Factors on Germination and Emergence of Invasive Rumex confertus in Central Europe. |
| Q45864607 | Effect of phosphorus availability on the selection of species with different ploidy levels and genome sizes in a long-term grassland fertilization experiment |
| Q93165271 | Effects of Temperature Treatments on Cytosine-Methylation Profiles of Diploid and Autotetraploid Plants of the Alpine Species Ranunculus kuepferi (Ranunculaceae) |
| Q59800050 | Effects of ploidy variation on promoter DNA methylation and gene expression in rice (Oryza sativa L.) |
| Q91912367 | Effects of soil nitrogen on diploid advantage in fireweed, Chamerion angustifolium (Onagraceae) |
| Q47170930 | Empirical evidence of fixed and homeostatic patterns of polyploid advantage in a keystone grass exposed to drought and heat stress. |
| Q35061876 | Epigenetic rather than genetic factors may explain phenotypic divergence between coastal populations of diploid and tetraploid Limonium spp. (Plumbaginaceae) in Portugal |
| Q59006334 | Ethnobotany and Ethnomedicinal Uses, Chromosomal Status and Natural Propagation of Some Plants of Lahaul-Spiti and Adjoining Hills |
| Q28661140 | Evolutionary consequences, constraints and potential of polyploidy in plants |
| Q33564771 | Evolutionary dynamics of tree invasions: complementing the unified framework for biological invasions |
| Q46890315 | Evolutionary history of two divergent Dmrt1 genes reveals two rounds of polyploidy origins in gibel carp |
| Q110951156 | Evolutionary importance of the relationship between cytogeography and climate: New insights on creosote bushes from North and South America |
| Q51148917 | Expansive reed populations-alien invasion or disturbed wetlands? |
| Q38614968 | Extensive analysis of native and non-native Centaurea solstitialis L. populations across the world shows no traces of polyploidization. |
| Q28830316 | Extensive variation, but not local adaptation in an Australian alpine daisy |
| Q57040210 | Functional trait divergence and trait plasticity confer polyploid advantage in heterogeneous environments |
| Q36246645 | GBS-based single dosage markers for linkage and QTL mapping allow gene mining for yield-related traits in sugarcane |
| Q46613613 | Gene Duplicability of Core Genes Is Highly Consistent across All Angiosperms. |
| Q88562627 | Gene retention, fractionation and subgenome differences in polyploid plants |
| Q92005887 | Genes Encoding Teleost Fish Ligands and Associated Receptors Remained in Duplicate More Frequently than the Rest of the Genome |
| Q56689607 | Genetic and Biochemical Consequences of Polyploidy in Tragopogon |
| Q34507910 | Genetic diversity of natural orchardgrass (Dactylis glomerata L.) populations in three regions in Europe |
| Q42117310 | Genetic variability within and among populations of an invasive, exotic orchid |
| Q33578807 | Genome expression balance in a triploid trihybrid vertebrate |
| Q35923462 | Genome size and ploidy influence angiosperm species' biomass under nitrogen and phosphorus limitation |
| Q36192925 | Geographic Variation in Festuca rubra L. Ploidy Levels and Systemic Fungal Endophyte Frequencies. |
| Q64359178 | Global Diversity of the Brachypodium Species Complex as a Resource for Genome-Wide Association Studies Demonstrated for Agronomic Traits in Response to Climate |
| Q56451724 | Global approaches to addressing biofuel-related invasive species risks and incorporation into U.S. laws and policies |
| Q46243132 | Global grass (Poaceae) success underpinned by traits facilitating colonization, persistence and habitat transformation. |
| Q51547016 | High male incidence and evolutionary implications of triploid form in northeast Asia Carassius auratus complex. |
| Q39277442 | High-performance genotypes in an introduced plant: insights to future invasiveness |
| Q36103424 | Historical biogeography of the fern genus Deparia (Athyriaceae) and its relation with polyploidy. |
| Q46228888 | Hitting the right target: taxonomic challenges for, and of, plant invasions. |
| Q36833827 | Homeotic Genes and the ABCDE Model for Floral Organ Formation in Wheat |
| Q52308982 | Homoeolog-specific activation of genes for heat acclimation in the allopolyploid grass Brachypodium hybridum. |
| Q48183515 | Homoeologous exchanges cause extensive dosage-dependent gene expression changes in an allopolyploid crop |
| Q34511104 | Hybridisation is associated with increased fecundity and size in invasive taxa: meta-analytic support for the hybridisation-invasion hypothesis. |
| Q36240944 | Hybridization of common reed in North America? The answer is blowing in the wind |
| Q107670733 | Identifying evolutionary lineages in the Elaeocarpus obovatus complex: population genetics and morphometric analyses support a new subspecies, Elaeocarpus obovatus subsp. umbratilis, from northern Queensland, Australia |
| Q28710579 | Increased phenotypic plasticity to climate may have boosted the invasion success of polyploid Centaurea stoebe |
| Q34315227 | Increased population growth rate in invasive polyploid Centaurea stoebe in a common garden |
| Q36114581 | Interspecific hybridization in Cucumis leads to the divergence of phenotypes in response to low light and extended photoperiods. |
| Q104736822 | Introduced plants of Lupinus polyphyllus are larger but flower less frequently than conspecifics from the native range: Results of the first year |
| Q38838966 | Invasion Fosters Change: Independent Evolutionary Shifts in Reproductive Traits after Oxalis pes-caprae L. Introduction |
| Q35545561 | Invasion genetics of the Bermuda buttercup (Oxalis pes-caprae): complex intercontinental patterns of genetic diversity, polyploidy and heterostyly characterize both native and introduced populations |
| Q56334705 | Invasion success in polyploids: the role of inbreeding in the contrasting colonization abilities of diploid versus tetraploid populations ofCentaurea stoebes.l |
| Q91876931 | Invasion, isolation and evolution shape population genetic structure in Campanula rotundifolia |
| Q35072694 | Invasive and non-invasive congeners show similar trait shifts between their same native and non-native ranges |
| Q56379919 | Invasive tall annual willowherb (Epilobium brachycarpum C. Presl) in Central Europe originates from high mountain areas of western North America |
| Q46242082 | Karyotype analysis in Bignonieae (Bignoniaceae): chromosome numbers and heterochromatin |
| Q55008312 | Low genetic diversity contrasts with high phenotypic variability in heptaploid Spartina densiflora populations invading the Pacific coast of North America. |
| Q35958265 | Macroevolutionary dynamics in the early diversification of Asteraceae |
| Q89683391 | Metabolome and Transcriptome Analysis of Hexaploid Solidago canadensis Roots Reveals its Invasive Capacity Related to Polyploidy |
| Q34390364 | Microsatellite polymorphism among Chrysanthemum sp. polyploids: the influence of whole genome duplication |
| Q91874266 | Molecular Mechanism of Vegetative Growth Advantage in Allotriploid Populus |
| Q64117441 | Molecular basis underlying the successful invasion of hexaploid cytotypes of Solidago canadensis L.: Insights from integrated gene and miRNA expression profiling |
| Q102152269 | Morphological differentiation across the invasive range in Senecio madagascariensis populations |
| Q57070602 | Morphometric traits in the fine-leaved fescues depend on ploidy level: the case of L |
| Q35794381 | Multiple and mass introductions from limited origins: genetic diversity and structure of Solidago altissima in the native and invaded range |
| Q28606481 | Multiple origins of BBCC allopolyploid species in the rice genus (Oryza) |
| Q46287973 | Multispeed genome diploidization and diversification after an ancient allopolyploidization. |
| Q35777717 | Natural variation, differentiation, and genetic trade-offs of ecophysiological traits in response to water limitation in Brachypodium distachyon and its descendent allotetraploid B. hybridum (Poaceae). |
| Q34581250 | New pasture plants intensify invasive species risk |
| Q56979444 | Niche conservatism and spread of seaweed invasive lineages with different residence time in the Mediterranean Sea |
| Q46331229 | Niche differences may explain the geographic distribution of cytotypes in Erysimum mediohispanicum. |
| Q38607646 | No difference in plasticity between different ploidy levels in the Mediterranean herb Mercurialis annua |
| Q46251287 | Non-Additive Transcriptomic Responses to Inoculation with Rhizobia in a Young Allopolyploid Compared with Its Diploid Progenitors |
| Q64234793 | Nutrient Deficiency Tolerance in Citrus Is Dependent on Genotype or Ploidy Level |
| Q98225793 | Occurrence of apomictic conspecifics and ecological preferences rather than colonization history govern the geographic distribution of sexual Potentilla puberula |
| Q26764749 | Of dups and dinos: evolution at the K/Pg boundary |
| Q104561652 | On the Origin of Coexisting Species |
| Q46659193 | On the relative abundance of autopolyploids and allopolyploids |
| Q64232938 | Parental legacy, demography, and admixture influenced the evolution of the two subgenomes of the tetraploid Capsella bursa-pastoris (Brassicaceae) |
| Q36072699 | Patterns of abiotic niche shifts in allopolyploids relative to their progenitors |
| Q91907678 | Pervasive population genomic consequences of genome duplication in Arabidopsis arenosa |
| Q56384469 | Phenotypic plasticity and population differentiation in response to salinity in the invasive cordgrass Spartina densiflora |
| Q58126737 | Phenotypic plasticity of polyploid plant species promotes transgressive behaviour in their hybrids |
| Q36054101 | Phylogenetic and ecological patterns in nighttime transpiration among five members of the genus Rubus co-occurring in western Oregon |
| Q89187554 | Phylogenetics of Camelina Crantz. (Brassicaceae) and insights on the origin of gold-of-pleasure (Camelina sativa) |
| Q28661709 | Physiological and proteomic responses of diploid and tetraploid black locust (Robinia pseudoacacia L.) subjected to salt stress |
| Q113676620 | Pioneering polyploids: the impact of whole-genome duplication on biome shifting in New Zealand Coprosma (Rubiaceae) and Veronica (Plantaginaceae) |
| Q46526105 | Plant adaptive radiation mediated by polyploid plasticity in transcriptomes. |
| Q28654226 | Polyploid evolution of the Brassicaceae during the Cenozoic era |
| Q58099150 | Polyploidy and introgression in invasive giant knotweed (Fallopia sachalinensis) during the colonization of remote volcanic islands |
| Q28657583 | Polyploidy and novelty: Gottlieb's legacy |
| Q39045260 | Polyploidy enhances the occupation of heterogeneous environments through hydraulic related trade-offs in Atriplex canescens (Chenopodiaceae). |
| Q56455529 | Polyploidy, alien species and invasiveness in Polish angiosperms |
| Q35903267 | Population Genetic Structure and Reproductive Strategy of the Introduced Grass Centotheca lappacea in Tropical Land-Use Systems in Sumatra |
| Q90887574 | Population genetic structure, migration, and polyploidy origin of a medicinal species Gynostemma pentaphyllum (Cucurbitaceae) |
| Q64067237 | Postglacial colonization history reflects in the genetic structure of natural populations of in Europe |
| Q31082553 | Potential Implications of Climate Change on Aegilops Species Distribution: Sympatry of These Crop Wild Relatives with the Major European Crop Triticum aestivum and Conservation Issues |
| Q97519482 | Preferential Disomic Segregation and C. micrantha/C. medica Interspecific Recombination in Tetraploid 'Giant Key' Lime; Outlook for Triploid Lime Breeding |
| Q90055857 | Preferential gene retention increases the robustness of cold regulation in Brassicaceae and other plants after polyploidization |
| Q42587513 | Present-day sympatry belies the evolutionary origin of a high-order polyploid |
| Q92430170 | Qualidade polínica, anormalidades meióticas e poliploidia emSisyrinchium commutatum (Iridaceae) |
| Q56066500 | Recent autopolyploidization in a naturalized population of Mimulus guttatus (Phrymaceae) |
| Q36217940 | Recreating Stable Brachypodium hybridum Allotetraploids by Uniting the Divergent Genomes of B. distachyon and B. stacei |
| Q30052971 | Relatedness defies biogeography: the tale of two island endemics (Acacia heterophyllaandA. koa) |
| Q46241624 | Residence time, native range size, and genome size predict naturalization among angiosperms introduced to Australia |
| Q43563391 | Response to competition of bulbous geophyte Allium oleraceum differing in ploidy level. |
| Q36749791 | Rethinking phenotypic plasticity and its consequences for individuals, populations and species |
| Q43242118 | Role of adaptive and non-adaptive mechanisms forming complex patterns of genome size variation in six cytotypes of polyploid Allium oleraceum (Amaryllidaceae) on a continental scale |
| Q51531876 | Sensitivity to phosphorus limitation increases with ploidy level in a New Zealand snail. |
| Q52658996 | Sequence and functional characterization of MIRNA164 promoters from Brassica shows copy number dependent regulatory diversification among homeologs. |
| Q47894193 | Sexy males and sexless females: the origin of triploid apomicts |
| Q47744305 | Small genome separates native and invasive populations in an ecologically important cosmopolitan grass. |
| Q94461588 | Synthetic hybrids of six yeast species |
| Q28657578 | Tangled up in two: a burst of genome duplications at the end of the Cretaceous and the consequences for plant evolution |
| Q59146757 | Target Transportation of Auxin on Mesoporous Au/SiO2 Nanoparticles as a Method for Somaclonal Variation Increasing in Flax (L. usitatissimum L.) |
| Q35342459 | Tetrasomic recombination is surprisingly frequent in allotetraploid Arachis. |
| Q30315413 | The Genetic Paradox of Invasions revisited: the potential role of inbreeding × environment interactions in invasion success |
| Q94464415 | The Role of Transcriptional Regulation in Hybrid Vigor |
| Q38218016 | The causes and molecular consequences of polyploidy in flowering plants |
| Q35139018 | The contrasting effects of genome size, chromosome number and ploidy level on plant invasiveness: a global analysis |
| Q47813721 | The direct effects of plant polyploidy on the legume-rhizobia mutualism |
| Q38729078 | The effects of genome duplications in a community context |
| Q39305536 | The evolutionary significance of polyploidy |
| Q56526210 | The expansion of sterile Arundo donax (Poaceae) in southeastern Australia is accompanied by genotypic variation |
| Q62659224 | The global biogeography of polyploid plants |
| Q30861745 | The hidden side of plant invasions: the role of genome size |
| Q92981071 | The influence of experimentally induced polyploidy on the relationships between endopolyploidy and plant function in Arabidopsis thaliana |
| Q38823503 | The interplay between aridity and competition determines colonization ability, exclusion and ecological segregation in the heteroploid Brachypodium distachyon species complex |
| Q35560368 | The origin of unique diversity in deglaciated areas: traces of Pleistocene processes in north-European endemics from the Galium pusillum polyploid complex (Rubiaceae). |
| Q34368040 | The oxidative damage initiation hypothesis for meiosis |
| Q56388344 | The population genetics of the fundamental cytotype-shift in invasive Centaurea stoebe s.l.: genetic diversity, genetic differentiation and small-scale genetic structure differ between cytotypes but not between ranges |
| Q39943280 | Trait responses of invasive aquatic macrophyte congeners: colonizing diploid outperforms polyploid |
| Q92566079 | Trait-dependent resemblance of the flowering phenology and floral morphology of the allopolyploid Cardamine flexuosa to those of the parental diploids in natural habitats |
| Q96136255 | Transcriptional analyses reveal the molecular mechanism governing shade tolerance in the invasive plant Solidago canadensis |
| Q38429678 | Transcriptome analysis reveals plant response to colchicine treatment during on chromosome doubling |
| Q34668800 | Transcriptome divergence between introduced and native populations of Canada thistle, Cirsium arvense |
| Q92566121 | Transgenerational effects of inter-ploidy cross direction on reproduction and F2 seed development of Arabidopsis thaliana F1 hybrid triploids |
| Q92012429 | Transgressivity in Key Functional Traits Rather Than Phenotypic Plasticity Promotes Stress Tolerance in A Hybrid Cordgrass |
| Q51147612 | Transient Activation of Apomixis in Sexual Neotriploids May Retain Genomically Altered States and Enhance Polyploid Establishment. |
| Q34768807 | Two colonisation stages generate two different patterns of genetic diversity within native and invasive ranges of Ulex europaeus |
| Q34386479 | Two sides of the same coin? Rare and pest plants native to the United States and Canada. |
| Q38630217 | Use of genotyping-by-sequencing to determine the genetic structure in the medicinal plant chamomile, and to identify flowering time and alpha-bisabolol associated SNP-loci by genome-wide association mapping. |
| Q92311763 | Using digital organisms to study the evolutionary consequences of whole genome duplication and polyploidy |
| Q111630318 | Variation of genome size and the ribosomal DNA ITS region of Alternanthera philoxeroides (Amaranthaceae) in Argentina, the USA, and China |
| Q38952360 | What does the geography of parthenogenesis teach us about sex? |
| Q35489352 | What we still don't know about invasion genetics |
| Q38594942 | Whole genome duplications in plants: an overview from Arabidopsis |
| Q39537676 | Whole-genome duplication as a key factor in crop domestication |
| Q33906263 | Wider geographic distribution and higher diversity of hexaploids than tetraploids in Carassius species complex reveal recurrent polyploidy effects on adaptive evolution |
| Q90379720 | Widespread ancient whole-genome duplications in Malpighiales coincide with Eocene global climatic upheaval |
| Q34465043 | Widespread triploidy in Western North American aspen (Populus tremuloides) |
| Q61451131 | and Visualizing chromosome count data from plants |
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