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Polyploidy increases overall diversity despite higher turnover than diploids in the Brassicaceae
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/ajb2.1019openalex-snapshot
Constructing a broadly inclusive seed plant phylogeny
inferredcites →https://doi.org/10.1002/ajb2.1060openalex-snapshot
Impact of whole‐genome duplication events on diversification rates in angiosperms
inferredcites →https://doi.org/10.1002/ajb2.1212openalex-snapshot
Autopolyploid lineage shows climatic niche expansion but not divergence in Arabidopsis arenosa
inferredcites →https://doi.org/10.1002/ece3.1430openalex-snapshot
Ecological differentiation, lack of hybrids involving diploids, and asymmetric gene flow between polyploids in narrow contact zones of Senecio carniolicus (syn. Jacobaea carniolica, Asteraceae)
inferredcites →https://doi.org/10.1002/j.1537-2197.1938.tb09203.xopenalex-snapshot
CYTOLOGICAL CHARACTERISTICS ASSOCIATED WITH THE DIFFERENT GROWTH HABITS IN THE DICOTYLEDONS
inferredcites →https://doi.org/10.1002/j.1537-2197.1973.tb05955.xopenalex-snapshot
SEXUAL AND SUBSEXUAL SYSTEMS IN HOMOSPOROUS PTERIDOPHYTES: A NEW HYPOTHESIS
inferredcites →https://doi.org/10.1002/tax.595006openalex-snapshot
What we still don't know about polyploidy
inferredcites →https://doi.org/10.1007/978-1-4613-3069-1_13openalex-snapshot
Polyploidy in Angiosperms: Monocotyledons
inferredcites →https://doi.org/10.1007/978-1-4615-9585-4_6openalex-snapshot
Variation and Evolution in Plants: Progress During the Past Twenty Years
inferredcites →https://doi.org/10.1007/978-3-662-43550-2_8openalex-snapshot
An Introduction to Phylogenetic Path Analysis
inferredcites →https://doi.org/10.1007/s00606-006-0415-zopenalex-snapshot
Systematics and phylogeny of the Brassicaceae (Cruciferae): an overview
inferredcites →https://doi.org/10.1007/s00606-013-0920-9openalex-snapshot
Chromosome studies in southern species of Mimosa (Fabaceae, Mimosoideae) and their taxonomic and evolutionary inferences
inferredcites →https://doi.org/10.1007/s00606-018-1507-2openalex-snapshot
Brassicales: an update on chromosomal evolution and ancient polyploidy
inferredcites →https://doi.org/10.1016/j.cell.2007.10.022openalex-snapshot
The Evolutionary Consequences of Polyploidy
inferredcites →https://doi.org/10.1016/j.gde.2007.09.007openalex-snapshot
Consequences of genome duplication
inferredcites →https://doi.org/10.1016/j.pbi.2012.03.010openalex-snapshot
Rarely successful polyploids and their legacy in plant genomes
inferredcites →https://doi.org/10.1016/j.tplants.2016.01.024openalex-snapshot
Turnip Time Travels: Age Estimates in Brassicaceae
inferredcites →https://doi.org/10.1016/j.tree.2005.07.008openalex-snapshot
Genome duplication and the origin of angiosperms
inferredcites →https://doi.org/10.1038/44766openalex-snapshot
Inferring the historical patterns of biological evolution
inferredcites →https://doi.org/10.1038/hdy.2012.79openalex-snapshot
Polyploidy and its effect on evolutionary success: old questions revisited with new tools
inferredcites →https://doi.org/10.1038/nature06148openalex-snapshot
The grapevine genome sequence suggests ancestral hexaploidization in major angiosperm phyla
inferredcites →https://doi.org/10.1038/nature09916openalex-snapshot
Ancestral polyploidy in seed plants and angiosperms
inferredcites →https://doi.org/10.1038/nature11631openalex-snapshot
The global diversity of birds in space and time
inferredcites →https://doi.org/10.1038/nature25794openalex-snapshot
Global elevational diversity and diversification of birds
inferredcites →https://doi.org/10.1038/nplants.2016.115openalex-snapshot
Whole-genome duplication as a key factor in crop domestication
inferredcites →https://doi.org/10.1038/nrg.2017.26openalex-snapshot
The evolutionary significance of polyploidy
inferredcites →https://doi.org/10.1038/nrg1711openalex-snapshot
The advantages and disadvantages of being polyploid
inferredcites →https://doi.org/10.1038/nrg2600openalex-snapshot
The evolutionary significance of ancient genome duplications
inferredcites →https://doi.org/10.1073/pnas.0307901101openalex-snapshot
Ancient polyploidization predating divergence of the cereals, and its consequences for comparative genomics
inferredcites →https://doi.org/10.1073/pnas.0811575106openalex-snapshot
The frequency of polyploid speciation in vascular plants
inferredcites →https://doi.org/10.1073/pnas.0900906106openalex-snapshot
Plants with double genomes might have had a better chance to survive the Cretaceous–Tertiary extinction event
inferredcites →https://doi.org/10.1073/pnas.1404177111openalex-snapshot
Allopolyploidy, diversification, and the Miocene grassland expansion
inferredcites →https://doi.org/10.1073/pnas.1818058116openalex-snapshot
Macroevolutionary diversification rates show time dependency
inferredcites →https://doi.org/10.1080/10635150701607033openalex-snapshot
Estimating a Binary Character's Effect on Speciation and Extinction
inferredcites →https://doi.org/10.1086/285180openalex-snapshot
A Model for Divergent, Allopatric Speciation of Polyploid Pteridophytes Resulting from Silencing of Duplicate-Gene Expression
inferredcites →https://doi.org/10.1086/499251openalex-snapshot
Polyploidy and Diversification: A Phylogenetic Investigation in Rosaceae
inferredcites →https://doi.org/10.1086/677752openalex-snapshot
Polyploid Formation Shapes Flowering Plant Diversity
inferredcites →https://doi.org/10.1093/aob/mcm326openalex-snapshot
The Ups and Downs of Genome Size Evolution in Polyploid Species of Nicotiana (Solanaceae)
inferredcites →https://doi.org/10.1093/aob/mcz123openalex-snapshot
Temporal patterns of diversification in Brassicaceae demonstrate decoupling of rate shifts and mesopolyploidization events
inferredcites →https://doi.org/10.1093/bioinformatics/btg412openalex-snapshot
APE: Analyses of Phylogenetics and Evolution in R language
inferredcites →https://doi.org/10.1093/bioinformatics/btm538openalex-snapshot
GEIGER: investigating evolutionary radiations
inferredcites →https://doi.org/10.1093/bioinformatics/btu181openalex-snapshot
geiger v2.0: an expanded suite of methods for fitting macroevolutionary models to phylogenetic trees
inferredcites →https://doi.org/10.1093/gbe/evw251openalex-snapshot
The Evolution of Haploid Chromosome Numbers in the Sunflower Family
inferredcites →https://doi.org/10.1093/molbev/msl087openalex-snapshot
Toward a Global Phylogeny of the Brassicaceae
inferredcites →https://doi.org/10.1093/molbev/msu122openalex-snapshot
ChromEvol: Assessing the Pattern of Chromosome Number Evolution and the Inference of Polyploidy along a Phylogeny
inferredcites →https://doi.org/10.1093/oso/9780198546412.001.0001openalex-snapshot
The Comparative Method in Evolutionary Biology
inferredcites →https://doi.org/10.1093/sysbio/syp067openalex-snapshot
Estimating Trait-Dependent Speciation and Extinction Rates from Incompletely Resolved Phylogenies
inferredcites →https://doi.org/10.1093/sysbio/syp083openalex-snapshot
Probabilistic Models of Chromosome Number Evolution and the Inference of Polyploidy
inferredcites →https://doi.org/10.1093/sysbio/syw022openalex-snapshot
Detecting Hidden Diversification Shifts in Models of Trait-Dependent Speciation and Extinction
inferredcites →https://doi.org/10.1098/rspb.2016.1334openalex-snapshot
Diversification rates and species richness across the Tree of Life
inferredcites →https://doi.org/10.1101/369124openalex-snapshot
Tip rates, phylogenies, and diversification: what are we estimating, and how good are the estimates?
inferredcites →https://doi.org/10.1101/709329openalex-snapshot
Interaction Between Ploidy, Breeding System, and Lineage Diversification
inferredcites →https://doi.org/10.1101/gr.168997.113openalex-snapshot
Analysis of 41 plant genomes supports a wave of successful genome duplications in association with the Cretaceous–Paleogene boundary
inferredcites →https://doi.org/10.1105/tpc.021345openalex-snapshot
Widespread Paleopolyploidy in Model Plant Species Inferred from Age Distributions of Duplicate Genes[W]
inferredcites →https://doi.org/10.1105/tpc.15.00482openalex-snapshot
A Time-Calibrated Road Map of Brassicaceae Species Radiation and Evolutionary History
inferredcites →https://doi.org/10.1109/tac.1974.1100705openalex-snapshot
A new look at the statistical model identification
inferredcites →https://doi.org/10.1111/ele.12438openalex-snapshot
Relative roles of ecological and energetic constraints, diversification rates and region history on global species richness gradients
inferredcites →https://doi.org/10.1111/ele.13402openalex-snapshot
Polyploid plants have faster rates of multivariate niche differentiation than their diploid relatives
inferredcites →https://doi.org/10.1111/j.0014-3820.2001.tb00826.xopenalex-snapshot
ABSOLUTE DIVERSIFICATION RATES IN ANGIOSPERM CLADES
inferredcites →https://doi.org/10.1111/j.0014-3820.2006.tb01198.xopenalex-snapshot
ON THE ABUNDANCE OF POLYPLOIDS IN FLOWERING PLANTS
inferredcites →https://doi.org/10.1111/j.1523-1739.2010.01455.xopenalex-snapshot
Selectivity in Mammalian Extinction Risk and Threat Types: a New Measure of Phylogenetic Signal Strength in Binary Traits
inferredcites →https://doi.org/10.1111/j.2041-210x.2011.00169.xopenalex-snapshot
phytools: an R package for phylogenetic comparative biology (and other things)
inferredcites →https://doi.org/10.1111/j.2041-210x.2012.00234.xopenalex-snapshot
Diversitree: comparative phylogenetic analyses of diversification in R
inferredcites →https://doi.org/10.1111/jbi.12085openalex-snapshot
Divergent and narrower climatic niches characterize polyploid species of European primroses inPrimulasect.Aleuritia
inferredcites →https://doi.org/10.1111/jeb.12308openalex-snapshot
Comparative analysis reveals that polyploidy does not decelerate diversification in fish
inferredcites →https://doi.org/10.1111/nph.12756openalex-snapshot
Are polyploids really evolutionary dead‐ends (again)? A critical reappraisal of Mayrose et al . (2011)
inferredcites →https://doi.org/10.1111/nph.13191openalex-snapshot
The Chromosome Counts Database ( CCDB ) – a community resource of plant chromosome numbers
inferredcites →https://doi.org/10.1111/nph.13192openalex-snapshot
Methods for studying polyploid diversification and the dead end hypothesis: a reply to Soltis et al . (2014)
inferredcites →https://doi.org/10.1111/nph.13264openalex-snapshot
A metacalibrated time‐tree documents the early rise of flowering plant phylogenetic diversity
inferredcites →https://doi.org/10.1111/nph.13698openalex-snapshot
On the relative abundance of autopolyploids and allopolyploids
inferredcites →https://doi.org/10.1111/nph.14069openalex-snapshot
Patterns of abiotic niche shifts in allopolyploids relative to their progenitors
inferredcites →https://doi.org/10.1111/nph.15357openalex-snapshot
Widespread ancient whole‐genome duplications in Malpighiales coincide with Eocene global climatic upheaval
inferredcites →https://doi.org/10.1126/science.1207205openalex-snapshot
Recently Formed Polyploid Plants Diversify at Lower Rates
inferredcites →https://doi.org/10.1146/annurev-arplant-042916-041040openalex-snapshot
Sequencing and Analyzing the Transcriptomes of a Thousand Species Across the Tree of Life for Green Plants
inferredcites →https://doi.org/10.1146/annurev.arplant.043008.092039openalex-snapshot
The Role of Hybridization in Plant Speciation
inferredcites →https://doi.org/10.1146/annurev.genet.34.1.401openalex-snapshot
POLYPLOID INCIDENCE AND EVOLUTION
inferredcites →https://doi.org/10.1186/s12864-017-3555-3openalex-snapshot
Plastome phylogeny and early diversification of Brassicaceae
inferredcites →https://doi.org/10.2179/0008-7475(2008)73[74:dpdbpg]2.0.co;2openalex-snapshot
Does Phylogenetic Distance Between Parental Genomes Govern the Success of Polyploids
inferredcites →https://doi.org/10.2307/1217945openalex-snapshot
BIOSYSTEMATICS AND EVOLUTIONARY NOISE
inferredcites →https://doi.org/10.2478/abcsb-2014-0001openalex-snapshot
Chromosome Numbers and Polyploidy in Life Forms of Asteraceae, Poaceae and Rosaceae in Polish Flora
inferredcites →https://doi.org/10.32614/cran.package.chromeropenalex-snapshot
chromer: Interface to Chromosome Counts Database API
inferredcites →https://doi.org/10.3389/fevo.2018.00117openalex-snapshot
The “Polyploid Hop”: Shifting Challenges and Opportunities Over the Evolutionary Lifespan of Genome Duplications
inferredcites →https://doi.org/10.3732/ajb.0800065openalex-snapshot
Brassicaceae phylogeny inferred from phytochrome A and ndhF sequence data: tribes and trichomes revisited
inferredcites →https://doi.org/10.3732/ajb.0800079openalex-snapshot
Polyploidy and angiosperm diversification
inferredcites →https://doi.org/10.3732/ajb.1300417openalex-snapshot
Climate niche modeling in the perennial Glycine (Leguminosae) allopolyploid complex
inferredcites →https://doi.org/10.3732/ajb.1400184openalex-snapshot
Climatic niche differences between diploid and tetraploid cytotypes of Chamerion angustifolium (Onagraceae)
inferredcites →https://doi.org/10.3732/ajb.1500052openalex-snapshot
Cytotype distribution patterns, ecological differentiation, and genetic structure in a diploid–tetraploid contact zone of Cardamine amara
inferredcites →https://doi.org/10.3732/ajb.1500128openalex-snapshot
Environmental niche variation and evolutionary diversification of the Brachypodium distachyon grass complex species in their native circum‐Mediterranean range
inferredcites →https://doi.org/10.3732/ajb.1600108openalex-snapshot
Phylogenetic evidence for cladogenetic polyploidization in land plants
inferredcites →https://doi.org/10.3732/ajb.1600130openalex-snapshot
Niche divergence between diploid and autotetraploid Tolmiea
inferredcites →https://doi.org/10.3732/ajb.89.11.1826openalex-snapshot
Phylogeny of Capparaceae and Brassicaceae based on chloroplast sequence data
inferredcites →https://doi.org/10.3732/ajb.93.4.607openalex-snapshot
Brassicaceae phylogeny and trichome evolution
inferredcites →https://doi.org/10.7717/peerj.4473openalex-snapshot
pcr: an R package for quality assessment, analysis and testing of qPCR data
inferredcites →https://doi.org/10.7717/peerj.4718openalex-snapshot
phylopath : Easy phylogenetic path analysis in R
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1007/978-981-15-6345-4_1openalex-snapshot
The Plant Family Brassicaceae: Introduction, Biology, And Importance
inferred← citeshttps://doi.org/10.1534/g3.120.401493openalex-snapshot
Genome-Wide Duplication of Allotetraploid Brassica napus Produces Novel Characteristics and Extensive Ploidy Variation in Self-Pollinated Progeny
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