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Evolution of sexual systems and growth habit in Mussaenda (Rubiaceae): Insights into the evolutionary pathways of dioecy
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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/10.1006/anbo.1999.1067openalex-snapshot
The Evolution and Function of Stylar Polymorphisms in Flowering Plants
inferredcites →https://doi.org/10.1006/bijl.1998.0219openalex-snapshot
Reproductive trait variation in the functionally dioecious and morphologically heterostylous island endemic Chassalia corallioides (Rubiaceae)
inferredcites →https://doi.org/10.1007/978-3-540-68486-2_1openalex-snapshot
New Insights on Heterostyly: Comparative Biology, Ecology and Genetics
inferredcites →https://doi.org/10.1007/978-3-642-83962-7openalex-snapshot
Molecular Techniques in Taxonomy
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DNA Protocols for Plants
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Heterostylous Genetic Polymorphisms: Model Systems for Evolutionary Analysis
inferredcites →https://doi.org/10.1007/978-3-642-86656-2_6openalex-snapshot
The Evolution of Heterostyly
inferredcites →https://doi.org/10.1007/978-3-662-03908-3openalex-snapshot
Gender and Sexual Dimorphism in Flowering Plants
inferredcites →https://doi.org/10.1007/978-3-662-03908-3_3openalex-snapshot
Empirical Studies: Evolution and Maintenance of Dimorphic Breeding Systems
inferredcites →https://doi.org/10.1007/978-3-662-03908-3_4openalex-snapshot
Theories of the Evolution of Sexual Dimorphism
inferredcites →https://doi.org/10.1007/bf00984123openalex-snapshot
Evolution towards dioecy in heterostylous populations
inferredcites →https://doi.org/10.1007/s00606-011-0588-yopenalex-snapshot
Functional dioecy in Morinda parvifolia (Rubiaceae), a species with stigma-height dimorphism
inferredcites →https://doi.org/10.1007/s11258-004-0057-6openalex-snapshot
Patterns of male sterility within and among populations of the distylous shrub Erythroxylum havanense (erythroxylaceae)
inferredcites →https://doi.org/10.1016/0040-5809(76)90050-2openalex-snapshot
The transmission of genes via pollen and ovules in gynodioecious angiosperms
inferredcites →https://doi.org/10.1016/j.ympev.2008.07.018openalex-snapshot
Phylogeny of Nolana (Solanaceae) of the Atacama and Peruvian deserts inferred from sequences of four plastid markers and the nuclear LEAFY second intron
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/j.ympev.2012.01.009openalex-snapshot
Phylogenetic insights into the correlates of dioecy in meadow-rues (Thalictrum, Ranunculaceae)
inferredcites →https://doi.org/10.1016/j.ympev.2014.05.022openalex-snapshot
Phylogenetic position of Guihaiothamnus (Rubiaceae): Its evolutionary and ecological implications
inferredcites →https://doi.org/10.1016/s0169-5347(02)02491-6openalex-snapshot
The ecology of lianas and their role in forests
inferredcites →https://doi.org/10.1016/s1360-1385(97)01012-1openalex-snapshot
Genetics of sex determination in flowering plants
inferredcites →https://doi.org/10.1017/cbo9780511897658.003openalex-snapshot
The distribution and evolution of climbing plants
inferredcites →https://doi.org/10.1038/nature14649openalex-snapshot
Parent–progeny sequencing indicates higher mutation rates in heterozygotes
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/10.1046/j.1442-1984.1999.00021.xopenalex-snapshot
Pollination system and evolution of dioecy from distyly in Mussaenda parviflora (Rubiaceae)
inferredcites →https://doi.org/10.1080/0028825x.1979.10432574openalex-snapshot
The biology of heterostyly
inferredcites →https://doi.org/10.1080/10635150490522304openalex-snapshot
Model Selection and Model Averaging in Phylogenetics: Advantages of Akaike Information Criterion and Bayesian Approaches Over Likelihood Ratio Tests
inferredcites →https://doi.org/10.1086/282748openalex-snapshot
The Concept of r- and K-Selection: Evidence from Wild Flowers and Some Theoretical Considerations
inferredcites →https://doi.org/10.1086/282864openalex-snapshot
Growth Form and Reproductive Effort in Goldenrods (Solidago, Compositae)
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A Model for the Evolution of Dioecy and Gynodioecy
inferredcites →https://doi.org/10.1086/283497openalex-snapshot
The Maintenance and Breakdown of Distyly
inferredcites →https://doi.org/10.1086/283837openalex-snapshot
Selection for Outcrossing, Sexual Selection, and the Evolution of Dioecy in Plants
inferredcites →https://doi.org/10.1086/283911openalex-snapshot
Five Evolutionary Pathways to Subdioecy
inferredcites →https://doi.org/10.1086/283959openalex-snapshot
Outcrossing Versus Ecological Constraints in the Evolution of Dioecy
inferredcites →https://doi.org/10.1086/283960openalex-snapshot
Outcrossing and the Incidence of Dioecism in Island Floras
inferredcites →https://doi.org/10.1086/284260openalex-snapshot
Some Functions of Dioecy in Seed Plants
inferredcites →https://doi.org/10.1086/303389openalex-snapshot
Lower Species Richness in Dioecious Clades
inferredcites →https://doi.org/10.1086/503444openalex-snapshot
Bayesian Analysis of Correlated Evolution of Discrete Characters by Reversible‐Jump Markov Chain Monte Carlo
inferredcites →https://doi.org/10.1093/aob/mcq146openalex-snapshot
Cryptic dioecy in Mussaenda pubescens (Rubiaceae): a species with stigma-height dimorphism
inferredcites →https://doi.org/10.1093/aob/mct053openalex-snapshot
Post-Boreotropical dispersals explain the pantropical disjunction in Paederia (Rubiaceae)
inferredcites →https://doi.org/10.1093/bioinformatics/btg180openalex-snapshot
MrBayes 3: Bayesian phylogenetic inference under mixed models
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/molbev/mss075openalex-snapshot
Bayesian Phylogenetics with BEAUti and the BEAST 1.7
inferredcites →https://doi.org/10.1093/sysbio/18.1.1openalex-snapshot
Quantitative Phyletics and the Evolution of Anurans
inferredcites →https://doi.org/10.1098/rspb.2004.2827openalex-snapshot
Evolution of a climbing habit promotes diversification in flowering 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.1996.0112openalex-snapshot
Effects of life history traits on genetic diversity in plant species
inferredcites →https://doi.org/10.1111/1365-2435.12274openalex-snapshot
Heterostyly promotes disassortative pollination and reduces sexual interference in Darwin's primroses: evidence from experimental studies
inferredcites →https://doi.org/10.1111/1442-1984.12013openalex-snapshot
Dioecy derived from distyly and pollination in Psychotria rubra ( R ubiaceae) occurring in the R yukyu I slands, J apan
inferredcites →https://doi.org/10.1111/boj.12038openalex-snapshot
Phylogenetic relationships and new tribal delimitations in subfamily Ixoroideae (Rubiaceae)
inferredcites →https://doi.org/10.1111/j.0014-3820.2002.tb00847.xopenalex-snapshot
THE EVOLUTION AND MAINTENANCE OF MONOECY AND DIOECY IN SAGITTARIA LATIFOLIA (ALISMATACEAE)
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.1096-0031.1989.tb00573.xopenalex-snapshot
THE RETENTION INDEX AND THE RESCALED CONSISTENCY INDEX
inferredcites →https://doi.org/10.1111/j.1420-9101.2005.00904.xopenalex-snapshot
Growth form evolution and shifting habitat specialization in annual plants
inferredcites →https://doi.org/10.1111/j.1438-8677.2009.00242.xopenalex-snapshot
Cryptic self‐incompatibility and distyly in Hedyotis acutangula Champ. (Rubiaceae)
inferredcites →https://doi.org/10.1111/j.1467-7652.2007.00245.xopenalex-snapshot
The complete nucleotide sequence of the coffee ( Coffea arabica L.) chloroplast genome: organization and implications for biotechnology and phylogenetic relationships amongst angiosperms
inferredcites →https://doi.org/10.1111/j.1469-185x.1942.tb00431.xopenalex-snapshot
THE EVOLUTION OF SEX IN FLOWERING PLANTS
inferredcites →https://doi.org/10.1111/j.1469-8137.1975.tb01346.xopenalex-snapshot
BREEDING SYSTEMS IN COTULA IV. REVERSION FROM DIOECY TO MONOECY
inferredcites →https://doi.org/10.1111/j.1469-8137.2012.04158.xopenalex-snapshot
Menispermaceae and the diversification of tropical rainforests near the Cretaceous–Paleogene boundary
inferredcites →https://doi.org/10.1111/j.1558-5646.1980.tb04055.xopenalex-snapshot
ROLE OF POLLINATORS IN THE EVOLUTION OF DIOECY FROM DISTYLY
inferredcites →https://doi.org/10.1111/j.1558-5646.1980.tb04795.xopenalex-snapshot
THE DISTRIBUTIONS OF GENDER IN FOUR ANGIOSPERM SPECIES ILLUSTRATING TWO EVOLUTIONARY PATHWAYS TO DIOECY
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.1558-5646.1985.tb00420.xopenalex-snapshot
CONFIDENCE LIMITS ON PHYLOGENIES: AN APPROACH USING THE BOOTSTRAP
inferredcites →https://doi.org/10.1111/j.1558-5646.1985.tb00455.xopenalex-snapshot
ON IRREVERSIBLE EVOLUTION
inferredcites →https://doi.org/10.1111/j.1558-5646.1994.tb02224.xopenalex-snapshot
NUCLEO-CYTOPLASMIC MALE STERILITY AND ALTERNATIVE ROUTES TO DIOECY
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/jeb.12385openalex-snapshot
Dioecy is associated with higher diversification rates in flowering plants
inferredcites →https://doi.org/10.1111/jipb.12140openalex-snapshot
Pre‐ and post‐zygotic reproductive isolation between co‐occurring Mussaenda pubescens var. alba and M. shikokiana (Rubiaceae)
inferredcites →https://doi.org/10.1111/jipb.12325openalex-snapshot
Reproductive isolation between sympatric sister species, Mussaenda kwangtungensis and M. pubescens var. alba
inferredcites →https://doi.org/10.1111/jse.12031openalex-snapshot
Self‐pollination in buds and homostyly in Mussaenda shikokiana ( R ubiaceae), a monomorphic species in a distylous clade
inferredcites →https://doi.org/10.1111/jse.12142openalex-snapshot
Distyly and cryptic heteromorphic self‐incompatibility inMussaenda macrophylla(Rubiaceae)
inferredcites →https://doi.org/10.1146/annurev.es.11.110180.000311openalex-snapshot
Evolution of Dioecy in Flowering Plants
inferredcites →https://doi.org/10.11646/phytotaxa.265.2.9openalex-snapshot
Mussaenda campanulata (Rubiaceae), a new monomorphic species from China
inferredcites →https://doi.org/10.1177/117693430600200024openalex-snapshot
LASER: A Maximum Likelihood Toolkit for Detecting Temporal Shifts in Diversification Rates from Molecular Phylogenies
inferredcites →https://doi.org/10.1186/1471-2148-7-214openalex-snapshot
BEAST: Bayesian evolutionary analysis by sampling trees
inferredcites →https://doi.org/10.1201/9780429310720-10openalex-snapshot
The Evolutionary Breakdown of Heterostyly
inferredcites →https://doi.org/10.1371/journal.pbio.0040088openalex-snapshot
Relaxed Phylogenetics and Dating with Confidence
inferredcites →https://doi.org/10.1371/journal.pone.0040851openalex-snapshot
Evolution of Growth Habit, Inflorescence Architecture, Flower Size, and Fruit Type in Rubiaceae: Its Ecological and Evolutionary Implications
inferredcites →https://doi.org/10.1371/journal.pone.0115653openalex-snapshot
Correlations of Life Form, Pollination Mode and Sexual System in Aquatic Angiosperms
inferredcites →https://doi.org/10.14601/phytopathol_mediterr-14998u1.29openalex-snapshot
BIOEDIT: A USER-FRIENDLY BIOLOGICAL SEQUENCE ALIGNMENT EDITOR AND ANALYSIS PROGRAM FOR WINDOWS 95/98/ NT
inferredcites →https://doi.org/10.2307/2412407openalex-snapshot
Quantitative Phyletics and the Evolution of Anurans
inferredcites →https://doi.org/10.2307/2426124openalex-snapshot
Effects of Pollen Vector and Plant Geometry on Floral Sex Ratio in Monoecious Plants
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/10.2307/3668266openalex-snapshot
Pseudomussaenda and Schizomussaenda (Rubiaceae): Close Allies of Mussaenda
inferredcites →https://doi.org/10.3389/fgene.2014.00452openalex-snapshot
Global diversification of a tropical plant growth form: environmental correlates and historical contingencies in climbing palms
inferredcites →https://doi.org/10.3417/2006191openalex-snapshot
Evolutionary Trends, Major Lineages, and New Generic Limits in the Dioecious Group of the Tribe Vanguerieae (Rubiaceae): Insights into the Evolution of Functional Dioecy1
inferredcites →https://doi.org/10.3732/ajb.1400196openalex-snapshot
The relative and absolute frequencies of angiosperm sexual systems: Dioecy, monoecy, gynodioecy, and an updated online database
inferredcites →https://doi.org/10.3732/ajb.90.3.404openalex-snapshot
Allometry and development in herbaceous plants: functional responses of meristem allocation to light and nutrient availability
inferredcites →https://doi.org/10.3732/ajb.92.1.142openalex-snapshot
The tortoise and the hare II: relative utility of 21 noncoding chloroplast DNA sequences for phylogenetic analysis
inferredcites →https://doi.org/10.3732/ajb.92.3.544openalex-snapshot
Polyphyly of Mussaenda inferred from ITS and trnT‐F data and its implication for generic limits in Mussaendeae (Rubiaceae)
inferredcites →https://doi.org/10.3732/ajb.92.7.1068openalex-snapshot
The evolution of unisexual flowers: morphological and functional convergence results from diverse developmental transitions
inferredcites →https://doi.org/10.3732/ajb.94.3.275openalex-snapshot
Comparison of whole chloroplast genome sequences to choose noncoding regions for phylogenetic studies in angiosperms: the tortoise and the hare III
inferredcites →https://doi.org/10.3767/000651908x608025openalex-snapshot
Revision of Schizomussaenda (Rubiaceae)
inferredcites →https://doi.org/10.5962/bhl.title.110054openalex-snapshot
The different forms of flowers on plants of the same species /
inferredcites →https://doi.org/10.5962/p.185680openalex-snapshot
The Rubiaceous Genus Mussaenda: the Species of the Philippine Islands
inferredcites →https://doi.org/10.5962/p.325961openalex-snapshot
Contribution à l'étude biologique et taxonomique des Mussendeae (Rubiaceae) d'Afrique Tropicale
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/ece3.6768openalex-snapshot
In situ glacial survival maintains high genetic diversity of Mussaenda kwangtungensis on continental islands in subtropical China
inferred← citeshttps://doi.org/10.1002/tax.13167openalex-snapshot
Phylogeny and classification of the coffee family (Rubiaceae, Gentianales): Overview and outlook
inferred← citeshttps://doi.org/10.1007/s00606-020-01698-0openalex-snapshot
Gynodioecy or leaky dioecy? The unusual sexual system of a coral dune-habitant Tournefortia argentea (Boraginaceae)
inferred← citeshttps://doi.org/10.1007/s00606-024-01932-zopenalex-snapshot
Consistency in patterns of pollen sterility between floral morphs in distylous populations of Erythroxylum (Erythroxylaceae)
inferred← citeshttps://doi.org/10.1007/s10265-023-01492-2openalex-snapshot
Long-and short-billed hummingbirds as pollinators of Palicourea demissa, a distylous treelet of Neotropical cloud forests
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/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/syab083openalex-snapshot
Pulled Diversification Rates, Lineages-Through-Time Plots, and Modern Macroevolutionary Modeling
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/10.1111/brv.70043openalex-snapshot
Reversibility of sex changes in the plant kingdom: more important than we thought?
inferred← citeshttps://doi.org/10.1111/njb.02523openalex-snapshot
Mussaenda yunnanensis sp. nov. (Rubiaceae), a new functionally dioecious species from Yunnan, China
inferred← citeshttps://doi.org/10.1111/nph.16026openalex-snapshot
‘A most complex marriage arrangement’: recent advances on heterostyly and unresolved questions
inferred← citeshttps://doi.org/10.1111/nph.70311openalex-snapshot
Genomic evidence unveils the genetic architecture and evolution of the S‐locus controlling heterostyly in Rubiaceae
inferred← citeshttps://doi.org/10.1111/nph.70521openalex-snapshot
Genetic architecture of the S ‐locus supergene revealed in a tetraploid distylous species
inferred← citeshttps://doi.org/10.1111/plb.13310openalex-snapshot
Variation in pollen sterility and gender specialization: an investigation with distylous species of Erythroxylum (Erythroxylaceae)
inferred← citeshttps://doi.org/10.1371/journal.pone.0232295openalex-snapshot
Chloroplast genomes of Rubiaceae: Comparative genomics and molecular phylogeny in subfamily Ixoroideae
inferred← citeshttps://doi.org/10.1590/0102-33062021abb0242openalex-snapshot
Evolution of distyly breakdown in Palicoureeae Robbr. & Manen and Psychotrieae Cham. & Schltdl. (Rubiaceae)
inferred← citeshttps://doi.org/10.28979/jarnas.1162623openalex-snapshot
The role of PCD in sexual dimorphism of dioecious Spinacia oleracea L.
inferred← citeshttps://doi.org/10.3389/fpls.2019.01315openalex-snapshot
Pollinator Behavior Drives Sexual Specializations in the Hermaphrodite Flowers of a Heterodichogamous Tree
inferred← citeshttps://doi.org/10.70675/f7015cdez0ad2z460cz8a9bza337e41b4296openalex-snapshot
Écologie des Rubiacées des Petites Antilles : le cas de la Martinique
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