Every reference with a DOI in the deposited reference list resolved to a known
work in Crossref or DataCite at the dated check, and none carried a retraction,
withdrawal, or removal notice.
The 104 checked references that resolve
resolves10.1073/pnas.0811087106Nine exceptional radiations plus high turnover explain species diversity in jawed vertebrates
resolves10.1111/nph.13698On the relative abundance of autopolyploids and allopolyploids
resolves10.3732/ajb.1600272Spreading Winge and flying high: The evolutionary importance of polyploidy after a century of study
resolves10.3732/ajb.1600113Most Compositae (Asteraceae) are descendants of a paleohexaploid and all share a paleotetraploid ancestor with the Calyceraceae
resolves10.1111/evo.13305Diversification rates are more strongly related to microhabitat than climate in squamate reptiles (lizards and snakes)
resolves10.1093/sysbio/syw022Detecting Hidden Diversification Shifts in Models of Trait-Dependent Speciation and Extinction
resolves10.1093/sysbio/syv027Heterogeneous Rates of Molecular Evolution and Diversification Could Explain the Triassic Age Estimate for Angiosperms
resolves10.1105/tpc.021345Widespread Paleopolyploidy in Model Plant Species Inferred from Age Distributions of Duplicate Genes[W]
resolves10.1126/science.1240561Polyploids Exhibit Higher Potassium Uptake and Salinity Tolerance in
<i>Arabidopsis</i>
resolves10.1098/rspb.2017.0912Constraining the timing of whole genome duplication in plant evolutionary history
resolves10.1007/s00606-017-1416-9Time-calibrated phylogenetic trees establish a lag between polyploidisation and diversification in Nicotiana (Solanaceae)
resolves10.1101/gr.4825606Widespread genome duplications throughout the history of flowering plants
resolves10.1186/1471-2148-13-38Exploring power and parameter estimation of the BiSSE method for analyzing species diversification
resolves10.1073/pnas.1300127110Convergent gene loss following gene and genome duplications creates single-copy families in flowering plants
resolves10.1111/boj.12357Is post-polyploidization diploidization the key to the evolutionary success of angiosperms?
resolves10.1111/nph.13367Confluence, synnovation, and depauperons in plant diversification
resolves10.1093/sysbio/syp067Estimating Trait-Dependent Speciation and Extinction Rates from Incompletely Resolved Phylogenies
resolves10.1086/284307Ecological Constraints on the Establishment of a Novel Polyploid in Competition with Its Diploid Progenitor
resolves10.1073/pnas.93.19.10274Substitution rate comparisons between grasses and palms: synonymous rate differences at the nuclear gene Adh parallel rate differences at the plastid gene rbcL.
resolves10.2307/3647457How many species of seed plants are there? ‐ a response
resolves10.1093/aob/mcu244Are tetraploids more successful? Floral signals, reproductive success and floral isolation in mixed-ploidy populations of a terrestrial orchid
resolves10.1371/journal.pone.0050284Increased Phenotypic Plasticity to Climate May Have Boosted the Invasion Success of Polyploid Centaurea stoebe
resolves10.1093/sysbio/syw021RevBayes: Bayesian Phylogenetic Inference Using Graphical Models and an Interactive Model-Specification Language
resolves10.1093/molbev/msw157Multiple Polyploidization Events across Asteraceae with Two Nested Events in the Early History Revealed by Nuclear Phylogenomics
resolves10.1093/sysbio/syu024Standard Sister Clade Comparison Fails when Testing Derived Character States
resolves10.1111/nph.13835Increased diversification rates follow shifts to bisexuality in liverworts
resolves10.2307/1218997MINORITY CYTOTYPE EXCLUSION IN LOCAL PLANT POPULATIONS
resolves10.1016/j.pbi.2017.09.010Factors promoting polyploid persistence and diversification and limiting diploid speciation during the K–Pg interlude
resolves10.1098/rspb.2013.2881A well-constrained estimate for the timing of the salmonid whole genome duplication reveals major decoupling from species diversification
resolves10.1038/hdy.2012.79Polyploidy and its effect on evolutionary success: old questions revisited with new tools
resolves10.1111/nph.13264A metacalibrated time‐tree documents the early rise of flowering plant phylogenetic diversity
resolves10.1186/s12862-015-0320-6Five major shifts of diversification through the long evolutionary history of Magnoliidae (angiosperms)
resolves10.1093/sysbio/syw026How Well Can We Detect Lineage-Specific Diversification-Rate Shifts? A Simulation Study of Sequential AIC Methods
resolves10.1111/nph.13192Methods for studying polyploid diversification and the dead end hypothesis: a reply to Soltis
<i>et al</i>
. (2014)
resolves10.1038/nplants.2016.119Transgressive phenotypes and generalist pollination in the floral evolution of Nicotiana polyploids
resolves10.1073/pnas.1518659113Critically evaluating the theory and performance of Bayesian analysis of macroevolutionary mixtures
resolves10.1111/jeb.12460How traits shape trees: new approaches for detecting character state‐dependent lineage diversification
resolves10.3732/ajb.1600012Past, future, and present of state‐dependent models of diversification
resolves10.1371/journal.pone.0120928Diversity Dynamics in Nymphalidae Butterflies: Effect of Phylogenetic Uncertainty on Diversification Rate Shift Estimates
resolves10.1093/jpe/rtv047An updated megaphylogeny of plants, a tool for generating plant phylogenies and an analysis of phylogenetic community structure
resolves10.1111/evo.12820Challenges in the estimation of extinction from molecular phylogenies: A response to Beaulieu and O'Meara
resolves10.1111/evo.13227FiSSE: A simple nonparametric test for the effects of a binary character on lineage diversification rates
resolves10.1111/2041-210X.12199<scp>BAMM</scp>tools: an R package for the analysis of evolutionary dynamics on phylogenetic trees
resolves10.1093/molbev/msr112Next Generation Sequencing Reveals Genome Downsizing in Allotetraploid Nicotiana tabacum, Predominantly through the Elimination of Paternally Derived Repetitive DNAs
resolves10.1086/677752Polyploid Formation Shapes Flowering Plant Diversity
resolves10.1016/j.pbi.2012.03.011Ancient whole genome duplications, novelty and diversification: the WGD Radiation Lag-Time Model
resolves10.1098/rspb.2016.2816Hummingbird pollination and the diversification of angiosperms: an old and successful association in Gesneriaceae
resolves10.3732/ajb.1000481Understanding angiosperm diversification using small and large phylogenetic trees
resolves10.1111/nph.13491Nested radiations and the pulse of angiosperm diversification: increased diversification rates often follow whole genome duplications
resolves10.1093/aob/mcr277The more the better? The role of polyploidy in facilitating plant invasions
resolves10.1038/nature11119The tomato genome sequence provides insights into fleshy fruit evolution
resolves10.1086/499251Polyploidy and Diversification: A Phylogenetic Investigation in Rosaceae
resolves10.3732/ajb.1500445Flower power and the mustard bomb: Comparative analysis of gene and genome duplications in glucosinolate biosynthetic pathway evolution in Cleomaceae and Brassicaceae
resolves10.1101/gr.168997.113Analysis of 41 plant genomes supports a wave of successful genome duplications in association with the Cretaceous–Paleogene boundary
resolves10.1016/j.ympev.2017.01.002Myrteae phylogeny, calibration, biogeography and diversification patterns: Increased understanding in the most species rich tribe of Myrtaceae
resolves10.1093/aob/mcs117Range expansion of a selfing polyploid plant despite widespread genetic uniformity
resolves10.1038/nature10625The Medicago genome provides insight into the evolution of rhizobial symbioses
resolves10.1038/nature12872Three keys to the radiation of angiosperms into freezing environments
resolves10.3732/ajb.1500408Evaluating the role of genome downsizing and size thresholds from genome size distributions in angiosperms
resolves10.1111/jeb.12308Comparative analysis reveals that polyploidy does not decelerate diversification in fish
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