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Dioecy is associated with higher diversification rates in flowering plants

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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/j.1537-2197.1995.tb11504.xopenalex-snapshot
D ioecy and its correlates in the flowering plants
inferredcites →https://doi.org/10.1007/bf01237724openalex-snapshot
Colonial breeding and speciation in birds
inferredcites →https://doi.org/10.1016/j.tree.2007.06.013openalex-snapshot
Estimating diversification rates from phylogenetic information
inferredcites →https://doi.org/10.1016/j.tree.2011.09.016openalex-snapshot
The many costs of sex
inferredcites →https://doi.org/10.1016/j.ympev.2005.10.002openalex-snapshot
Phylogeny of the Cucurbitales based on DNA sequences of nine loci from three genomes: Implications for morphological and sexual system evolution
inferredcites →https://doi.org/10.1016/j.ympev.2009.08.006openalex-snapshot
A three-genome phylogeny of Momordica (Cucurbitaceae) suggests seven returns from dioecy to monoecy and recent long-distance dispersal to Asia
inferredcites →https://doi.org/10.1016/s0169-5347(97)01273-1openalex-snapshot
Key innovations and the ecology of macroevolution
inferredcites →https://doi.org/10.1016/s1360-1385(97)01012-1openalex-snapshot
Genetics of sex determination in flowering plants
inferredcites →https://doi.org/10.1038/263125a0openalex-snapshot
Why be an hermaphrodite?
inferredcites →https://doi.org/10.1038/hdy.1994.181openalex-snapshot
Evolution of dioecy: can nuclear–cytoplasmic interactions select for maleness?
inferredcites →https://doi.org/10.1038/nrg2526openalex-snapshot
Effective population size and patterns of molecular evolution and variation
inferredcites →https://doi.org/10.1038/nrg776openalex-snapshot
The evolution of plant sexual diversity
inferredcites →https://doi.org/10.1046/j.1420-9101.2003.00559.xopenalex-snapshot
Phylogenetic analysis of the ecological correlates of dioecy in angiosperms
inferredcites →https://doi.org/10.1073/pnas.0308127100openalex-snapshot
Darwin's abominable mystery: Insights from a supertree of the angiosperms
inferredcites →https://doi.org/10.1073/pnas.0811087106openalex-snapshot
Nine exceptional radiations plus high turnover explain species diversity in jawed vertebrates
inferredcites →https://doi.org/10.1073/pnas.1016876108openalex-snapshot
Mammalian phylogeny reveals recent diversification rate shifts
inferredcites →https://doi.org/10.1073/pnas.1205818109openalex-snapshot
Phylogenomics and a posteriori data partitioning resolve the Cretaceous angiosperm radiation Malpighiales
inferredcites →https://doi.org/10.1080/0028825x.1979.10432573openalex-snapshot
Parental strategies of angiosperms
inferredcites →https://doi.org/10.1080/10635150701607033openalex-snapshot
Estimating a Binary Character's Effect on Speciation and Extinction
inferredcites →https://doi.org/10.1086/283342openalex-snapshot
A Model for the Evolution of Dioecy and Gynodioecy
inferredcites →https://doi.org/10.1086/285570openalex-snapshot
Diversification of Carnivorous Parasitic Insects: Extraordinary Radiation or Specialized Dead End?
inferredcites →https://doi.org/10.1086/285586openalex-snapshot
Testing Whether Certain Traits have Caused Amplified Diversification: An Improved Method Based on a Model of Random Speciation and Extinction
inferredcites →https://doi.org/10.1086/303303openalex-snapshot
Phylogenetic Analysis of Dioecy in Monocotyledons
inferredcites →https://doi.org/10.1086/303389openalex-snapshot
Lower Species Richness in Dioecious Clades
inferredcites →https://doi.org/10.1086/519856openalex-snapshot
Animal Dispersal Dynamics Promoting Dioecy over Hermaphroditism
inferredcites →https://doi.org/10.1086/599084openalex-snapshot
The Evolutionary Enigma of Sex
inferredcites →https://doi.org/10.1086/666649openalex-snapshot
Linking the Investigations of Character Evolution and Species Diversification
inferredcites →https://doi.org/10.1093/aob/mcp035openalex-snapshot
Wind of change: new insights on the ecology and evolution of pollination and mating in wind-pollinated plants
inferredcites →https://doi.org/10.1093/molbev/mss075openalex-snapshot
Bayesian Phylogenetics with BEAUti and the BEAST 1.7
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/syp069openalex-snapshot
Heritability of Extinction Rates Links Diversification Patterns in Molecular Phylogenies and Fossils
inferredcites →https://doi.org/10.1093/sysbio/syq053openalex-snapshot
Quantitative Traits and Diversification
inferredcites →https://doi.org/10.1093/sysbio/syr126openalex-snapshot
Multiple Continental Radiations and Correlates of Diversification in Lupinus (Leguminosae): Testing for Key Innovation with Incomplete Taxon Sampling
inferredcites →https://doi.org/10.1093/sysbio/sys031openalex-snapshot
A New Method for Handling Missing Species in Diversification Analysis Applicable to Randomly or Nonrandomly Sampled Phylogenies
inferredcites →https://doi.org/10.1093/sysbio/syu024openalex-snapshot
Standard Sister Clade Comparison Fails when Testing Derived Character States
inferredcites →https://doi.org/10.1098/rspb.2002.2004openalex-snapshot
When looks can kill: the evolution of sexually dimorphic floral display and the extinction of dioecious plants
inferredcites →https://doi.org/10.1098/rspb.2013.0913openalex-snapshot
The evolution of plant reproductive systems: how often are transitions irreversible?
inferredcites →https://doi.org/10.1098/rstb.1991.0070openalex-snapshot
Abiotic pollination: an evolutionary escape for animal-pollinated angiosperms
inferredcites →https://doi.org/10.1105/tpc.016667openalex-snapshot
Sex-Determining Mechanisms in Land Plants
inferredcites →https://doi.org/10.1111/j.0014-3820.2001.tb00605.xopenalex-snapshot
THE CONSEQUENCES OF DIOECY FOR SEED DISPERSAL: MODELING THE SEED-SHADOW HANDICAP
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.0014-3820.2004.tb00405.xopenalex-snapshot
THE ROLE OF DIVERSIFICATION IN CAUSING THE CORRELATES OF DIOECY
inferredcites →https://doi.org/10.1111/j.1095-8312.1981.tb00748.xopenalex-snapshot
Allocation of resources to male and female functions in hermaphrodites
inferredcites →https://doi.org/10.1111/j.1365-2699.2006.01504.xopenalex-snapshot
Anagenetic evolution in island plants
inferredcites →https://doi.org/10.1111/j.1469-8137.1972.tb01996.xopenalex-snapshot
BREEDING SYSTEMS IN COTULA L. (COMPOSITAE, ANTHEMIDEAE)
inferredcites →https://doi.org/10.1111/j.1558-5646.1980.tb04034.xopenalex-snapshot
ECOLOGICAL CONSTRAINTS ON THE EVOLUTION OF BREEDING SYSTEMS IN SEED PLANTS: DIOECY AND DISPERSAL IN GYMNOSPERMS
inferredcites →https://doi.org/10.1111/j.1558-5646.1982.tb05462.xopenalex-snapshot
INTRASEXUAL SELECTION AND THE SEGREGATION OF POLLEN AND STIGMAS IN HERMAPHRODITE PLANTS, EXEMPLIFIED BYWAHLENBERGIA ALBOMARGINATA(CAMPANULACEAE)
inferredcites →https://doi.org/10.1111/j.1558-5646.1994.tb02200.xopenalex-snapshot
SPECIES RICHNESS WITHIN FAMILIES OF FLOWERING PLANTS
inferredcites →https://doi.org/10.1111/j.1558-5646.1999.tb05367.xopenalex-snapshot
PHYLOGENETIC ANALYSIS OF TRAIT EVOLUTION AND SPECIES DIVERSITY VARIATION AMONG ANGIOSPERM FAMILIES
inferredcites →https://doi.org/10.1111/j.1558-5646.2011.01378.xopenalex-snapshot
LOSS OF SEXUAL RECOMBINATION AND SEGREGATION IS ASSOCIATED WITH INCREASED DIVERSIFICATION IN EVENING PRIMROSES
inferredcites →https://doi.org/10.1111/j.1558-5646.2012.01730.xopenalex-snapshot
TEMPO AND MODE IN PLANT BREEDING SYSTEM EVOLUTION
inferredcites →https://doi.org/10.1111/nph.12182openalex-snapshot
Is self‐fertilization an evolutionary dead end?
inferredcites →https://doi.org/10.1126/science.1091483openalex-snapshot
The Significance of Few Versus Many in the Tree of Life
inferredcites →https://doi.org/10.1126/science.1194513openalex-snapshot
Species Selection Maintains Self-Incompatibility
inferredcites →https://doi.org/10.1126/science.1207205openalex-snapshot
Recently Formed Polyploid Plants Diversify at Lower Rates
inferredcites →https://doi.org/10.1127/1869-6155/2010/0128-0011openalex-snapshot
Major events in the evolution of sexual systems in Apiales: ancestral andromonoecy abandoned
inferredcites →https://doi.org/10.1146/annurev-arplant-042110-103914openalex-snapshot
Sex Chromosomes in Land Plants
inferredcites →https://doi.org/10.1146/annurev.ecolsys.110308.120203openalex-snapshot
Flower Evolution: The Origin and Subsequent Diversification of the Angiosperm Flower
inferredcites →https://doi.org/10.1146/annurev.ecolsys.110308.120310openalex-snapshot
The Role of Animal Pollination in Plant Speciation: Integrating Ecology, Geography, and Genetics
inferredcites →https://doi.org/10.1146/annurev.es.02.110171.002341openalex-snapshot
Seed Predation by Animals
inferredcites →https://doi.org/10.1146/annurev.es.11.110180.000311openalex-snapshot
Evolution of Dioecy in Flowering Plants
inferredcites →https://doi.org/10.1146/annurev.es.18.110187.001321openalex-snapshot
INBREEDING DEPRESSION AND ITS EVOLUTIONARY CONSEQUENCES
inferredcites →https://doi.org/10.1186/1471-2148-10-109openalex-snapshot
The origins of species richness in the Hymenoptera: insights from a family-level supertree
inferredcites →https://doi.org/10.1186/1471-2148-12-108openalex-snapshot
Evolution and loss of long-fringed petals: a case study using a dated phylogeny of the snake gourds, Trichosanthes (Cucurbitaceae)
inferredcites →https://doi.org/10.1186/1471-2148-13-38openalex-snapshot
Exploring power and parameter estimation of the BiSSE method for analyzing species diversification
inferredcites →https://doi.org/10.1371/journal.pbio.0020183openalex-snapshot
Everything You Always Wanted to Know about Sexes
inferredcites →https://doi.org/10.1554/0014-3820(2001)055[0880:tcodfs]2.0.co;2openalex-snapshot
THE CONSEQUENCES OF DIOECY FOR SEED DISPERSAL: MODELING THE SEED-SHADOW HANDICAP
inferredcites →https://doi.org/10.1554/05-481.1openalex-snapshot
THE EVOLUTION OF GENDER SPECIALIZATION FROM DIMORPHIC HERMAPHRODITISM: PATHS FROM HETERODICHOGAMY TO GYNODIOECY AND ANDRODIOECY
inferredcites →https://doi.org/10.1890/0012-9658(1999)080[0116:eofhom]2.0.co;2openalex-snapshot
EFFECTS OF FOLIAR HERBIVORY ON MALE AND FEMALE REPRODUCTIVE TRAITS OF WILD RADISH,RAPHANUS RAPHANISTRUM
inferredcites →https://doi.org/10.2307/2412748openalex-snapshot
Expected Asymmetry of Phylogenetic Trees
inferredcites →https://doi.org/10.2307/2656594openalex-snapshot
Gender specialization in heterodichogamous Grayia brandegei (Chenopodiaceae): evidence for an alternative pathway to dioecy
inferredcites →https://doi.org/10.2307/2656726openalex-snapshot
Phylogenetic relationships of functionally dioecious FICUS (Moraceae) based on ribosomal DNA sequences and morphology
inferredcites →https://doi.org/10.2307/3079015openalex-snapshot
Phylogenetic Analysis of Dioecy in Monocotyledons
inferredcites →https://doi.org/10.2307/3079146openalex-snapshot
Lower Species Richness in Dioecious Clades
inferredcites →https://doi.org/10.2307/4541112openalex-snapshot
Animal Dispersal Dynamics Promoting Dioecy over Hermaphroditism
inferredcites →https://doi.org/10.3732/ajb.0800047openalex-snapshot
Reconstructing the ancestral angiosperm flower and its initial specializations
inferredcites →https://doi.org/10.3732/ajb.0800187openalex-snapshot
Hybridization, polyploidy, and evolutionary transitions between monoecy and dioecy in Bryonia (Cucurbitaceae)
inferredcites →https://doi.org/10.3732/ajb.1000311openalex-snapshot
Factors influencing diversification in angiosperms: At the crossroads of intrinsic and extrinsic traits
inferredcites →https://doi.org/10.3732/ajb.91.5.767openalex-snapshot
On the origin of the fig: phylogenetic relationships of Moraceae from ndhF sequences

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.5852/ejt.2023.888.2241zenodo-depositor-declared
Notes on cauliflory, sexual dimorphism and biogeography in Drypetes (Putranjivaceae, Malpighiales) and a taxonomic treatment for D. gabonensis and two new cauliflorous threatened species from Central Africa, D. aphanes sp. nov. and D. cauta sp. nov.
inferred← citeshttps://doi.org/10.1007/978-3-030-46012-9_9openalex-snapshot
Sex-Biased Herbivory and Its Effects on Tritrophic Interactions
inferred← citeshttps://doi.org/10.1007/978-3-319-94139-4_2openalex-snapshot
Phylogeny, Evolution, and Ecology of Sexual Systems Across the Land Plants
inferred← citeshttps://doi.org/10.1007/978-3-319-94139-4_3openalex-snapshot
Transitions Between Combined and Separate Sexes in Flowering Plants
inferred← citeshttps://doi.org/10.1007/s10531-023-02700-0openalex-snapshot
Uneven patterns of palm species loss due to climate change are not driven by their sexual systems
inferred← citeshttps://doi.org/10.1007/s11258-026-01631-4openalex-snapshot
Reproductive ecology of the dioecious endemic Erodium sibthorpianum subsp. sibthorpianum in Türkiye
inferred← citeshttps://doi.org/10.1007/s12228-023-09759-7openalex-snapshot
Miconia burkeae (Melastomataceae), a new dioecious tree from the montane forests of the Peruvian Andes
inferred← citeshttps://doi.org/10.1016/b978-0-12-800049-6.00161-xopenalex-snapshot
Mating Systems in Flowering Plants
inferred← citeshttps://doi.org/10.1016/b978-0-12-800049-6.00320-6openalex-snapshot
Mating Systems in Plants, Genome Evolution and
inferred← citeshttps://doi.org/10.1016/j.actao.2017.11.001openalex-snapshot
Rush hour at the Museum – Diversification patterns provide new clues for the success of figs (Ficus L., Moraceae)
inferred← citeshttps://doi.org/10.1016/j.baae.2018.05.009openalex-snapshot
Sexual systems in gymnosperms: A review
inferred← citeshttps://doi.org/10.1016/j.cub.2020.12.028openalex-snapshot
The rapid dissolution of dioecy by experimental evolution
inferred← citeshttps://doi.org/10.1016/j.ecolmodel.2022.110135openalex-snapshot
Transition model for the hermaphroditism-dioecy continuum in higher plants
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2017.11.005openalex-snapshot
Does sexual dimorphism in plants promote sex chromosome evolution?
inferred← citeshttps://doi.org/10.1016/j.isci.2023.106362openalex-snapshot
Opposing effects of plant traits on diversification
inferred← citeshttps://doi.org/10.1016/j.jep.2018.04.011openalex-snapshot
Ethnobotany of dioecious species: Traditional knowledge on dioecious plants in India
inferred← citeshttps://doi.org/10.1016/j.ympev.2018.02.015openalex-snapshot
Evolution of sexual systems and growth habit in Mussaenda (Rubiaceae): Insights into the evolutionary pathways of dioecy
inferred← citeshttps://doi.org/10.1016/j.ympev.2018.06.035openalex-snapshot
Evolution of floral traits and impact of reproductive mode on diversification in the phlox family (Polemoniaceae)
inferred← citeshttps://doi.org/10.1016/j.ympev.2023.107863openalex-snapshot
Genomic data provide a robust phylogeny backbone for Rhodiola L. (Crassulaceae) and reveal extensive reticulate evolution during its rapid radiation
inferred← citeshttps://doi.org/10.1038/s41437-020-00397-3openalex-snapshot
Sex determination through X–Y heterogamety in Salix nigra
inferred← citeshttps://doi.org/10.1038/s41477-024-01726-8openalex-snapshot
Transition of survival strategies under global climate shifts in the grape family
inferred← citeshttps://doi.org/10.1038/s41598-024-84367-3openalex-snapshot
Large range sizes link fast life histories with high species richness across wet tropical tree floras
inferred← citeshttps://doi.org/10.1038/s42003-024-06687-4openalex-snapshot
Key innovations and niche variation promoted rapid diversification of the widespread Juniperus (Cupressaceae)
inferred← citeshttps://doi.org/10.1086/697148openalex-snapshot
Explaining Ovule Sterility inRauvolfiaL. (Apocynaceae)
inferred← citeshttps://doi.org/10.1086/729063openalex-snapshot
Characterizing the Frequency, Morphological Gradient, and Distribution of Dioecy in Miconia (Melastomataceae)
inferred← citeshttps://doi.org/10.1093/aob/mcab056openalex-snapshot
In situradiation explains the frequency of dioecious palms on islands
inferred← citeshttps://doi.org/10.1093/aob/mcab129openalex-snapshot
Simulated herbivory enhances leaky sex expression in the dioecious herb Mercurialis annua
inferred← citeshttps://doi.org/10.1093/aob/mcac085openalex-snapshot
Macroevolutionary trends and diversification dynamics in Atripliceae (Amaranthaceae s.l., Chenopodioideae): a first approach
inferred← citeshttps://doi.org/10.1093/aob/mcu134openalex-snapshot
An angiosperm-wide analysis of the gynodioecy–dioecy pathway
inferred← citeshttps://doi.org/10.1093/aob/mcy159openalex-snapshot
Estimating divergence times and ancestral breeding systems inFicusand Moraceae
inferred← citeshttps://doi.org/10.1093/aobpla/plag031openalex-snapshot
Maternal sex influences seed dormancy in a gynodioecious species
inferred← citeshttps://doi.org/10.1093/botlinnean/boab032openalex-snapshot
Long-distance dispersal events rather than growth habit and life-history traits affect diversification rate in tribe Apieae (Apiaceae)
inferred← citeshttps://doi.org/10.1093/gbe/evw282openalex-snapshot
The Evolution of Sex Chromosomes and Dosage Compensation in Plants
inferred← citeshttps://doi.org/10.1093/molbev/msaa229openalex-snapshot
Dioecy Is Associated with High Genetic Diversity and Adaptation Rates in the Plant Genus Silene
inferred← citeshttps://doi.org/10.1093/sysbio/syu024openalex-snapshot
Standard Sister Clade Comparison Fails when Testing Derived Character States
inferred← citeshttps://doi.org/10.1098/rstb.2021.0224openalex-snapshot
Recurrent allopolyploidization, Y-chromosome introgression and the evolution of sexual systems in the plant genus Mercurialis
inferred← citeshttps://doi.org/10.1101/414771openalex-snapshot
Dioecy in plants: an evolutionary dead end? Insights from a population genomics study in the Silene genus
inferred← citeshttps://doi.org/10.1101/430041openalex-snapshot
A ghost of dioecy past and the legacy of sexual dimorphism: low siring success of hermaphrodites after the breakdown of dioecy
inferred← citeshttps://doi.org/10.1101/724377openalex-snapshot
Hybridization and diversification are positively correlated across vascular plant families
inferred← citeshttps://doi.org/10.1111/ele.13207openalex-snapshot
Low siring success of females with an acquired male function illustrates the legacy of sexual dimorphism in constraining the breakdown of dioecy
inferred← citeshttps://doi.org/10.1111/ele.13815openalex-snapshot
Global distribution and evolutionary transitions of angiosperm sexual systems
inferred← citeshttps://doi.org/10.1111/ele.14170openalex-snapshot
Trait‐dependent diversification in angiosperms: Patterns, models and data
inferred← citeshttps://doi.org/10.1111/evo.13181openalex-snapshot
Macroevolutionary synthesis of flowering plant sexual systems
inferred← citeshttps://doi.org/10.1111/evo.13245openalex-snapshot
Lineages ofSilene nutansdeveloped rapid, strong, asymmetric postzygotic reproductive isolation in allopatry
inferred← citeshttps://doi.org/10.1111/evo.14291openalex-snapshot
Limited evidence for a positive relationship between hybridization and diversification across seed plant families
inferred← citeshttps://doi.org/10.1111/jeb.12424openalex-snapshot
Sex uncovered: the evolutionary biology of reproductive systems
inferred← citeshttps://doi.org/10.1111/jvs.13291openalex-snapshot
Trait correlation and the assembly of island plant communities: Evidence from the Southwest Pacific
inferred← citeshttps://doi.org/10.1111/mec.14020openalex-snapshot
On the rarity of dioecy in flowering plants
inferred← citeshttps://doi.org/10.1111/mec.14540openalex-snapshot
Transitions in sex determination and sex chromosomes across vertebrate species
inferred← citeshttps://doi.org/10.1111/mec.16623openalex-snapshot
A low‐latitude species pump: Peripheral isolation, parapatric speciation and mating‐system evolution converge in a marine radiation
inferred← citeshttps://doi.org/10.1111/nph.13696openalex-snapshot
Dioecy does not consistently accelerate or slow lineage diversification across multiple genera of angiosperms
inferred← citeshttps://doi.org/10.1111/nph.13835openalex-snapshot
Increased diversification rates follow shifts to bisexuality in liverworts
inferred← citeshttps://doi.org/10.1111/nph.13926openalex-snapshot
Why is gynodioecy a rare but widely distributed sexual system? Lessons from the Lamiaceae
inferred← citeshttps://doi.org/10.1111/nph.15104openalex-snapshot
Key questions and challenges in angiosperm macroevolution
inferred← citeshttps://doi.org/10.1111/nph.70894openalex-snapshot
An angiosperm‐wide perspective on reproductive strategies and floral traits
inferred← citeshttps://doi.org/10.1146/annurev-arplant-042817-040348openalex-snapshot
Macroevolutionary Patterns of Flowering Plant Speciation and Extinction
inferred← citeshttps://doi.org/10.1186/s12862-025-02388-6openalex-snapshot
Experimental evidence of pollination by deception in a dioecious palm
inferred← citeshttps://doi.org/10.1186/s12870-026-08350-yopenalex-snapshot
Plastid genomes and phylogenomic relationships in Cheilosoideae, a poorly known early-diverging subfamily of Euphorbiaceae
inferred← citeshttps://doi.org/10.1270/jsbbs.22082openalex-snapshot
Evolution of sex in crops: recurrent scrap and rebuild
inferred← citeshttps://doi.org/10.17520/biods.2022065openalex-snapshot
Angiosperm sexual systems-Concepts, evolution, ecology, and future directions
inferred← citeshttps://doi.org/10.3389/fpls.2020.01222openalex-snapshot
Spatial Patterns and Drivers of Angiosperm Sexual Systems in China Differ Between Woody and Herbaceous Species
inferred← citeshttps://doi.org/10.3390/agriculture12030364openalex-snapshot
Dioecy in Flowering Plants: From the First Observations of Prospero Alpini in the XVI Century to the Most Recent Advances in the Genomics Era
inferred← citeshttps://doi.org/10.3732/ajb.1400196openalex-snapshot
The relative and absolute frequencies of angiosperm sexual systems: Dioecy, monoecy, gynodioecy, and an updated online database
inferred← citeshttps://doi.org/10.3732/ajb.1700289openalex-snapshot
More than sixty origins of pantoporate pollen in angiosperms
inferred← citeshttps://doi.org/10.64898/2026.06.13.732039openalex-snapshot
Organelle Capture, Lineage-Specific Genomic Responses, and the Lability of Dioecy in Amaranthus
inferred← citeshttps://doi.org/10.70675/38bac37bz8736z4009z995bz26579e2e8f89openalex-snapshot
Phylogeny, biogeography, and breeding system evolution in Moraceae
inferred← citeshttps://doi.org/10.70675/9f3944efzedfbz4cf6zb4e3zc229fb4ad00copenalex-snapshot
Pollinators : demanding partners : Investigating the interplay between plant-pollinator interactions and plant traits evolution
inferred← citeshttps://doi.org/10.70675/f3138083z60eez4bbcz84afz69529d38aa24openalex-snapshot
Cooperation and competition as drivers of the evolutionary transition from simultaneous hermaphroditism to separate sexes in Ophryotrocha worms
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