On the public citation graph

Whole genome duplication enables rapid evolution of male-biased sex allocation in Galax urceolata

https://doi.org/10.1101/2025.06.19.660553
0 signed · 89 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.
Claim with ORCID
Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/ajb2.1161openalex-snapshot
Climatic niche comparison among ploidal levels in the classic autopolyploid system, Galax urceolata
inferredcites →https://doi.org/10.1002/ajb2.1258openalex-snapshot
A meta‐analysis of whole genome duplication and the effects on flowering traits in plants
inferredcites →https://doi.org/10.1002/ajb2.1412openalex-snapshot
Active pollination drives selection for reduced pollen‐ovule ratios
inferredcites →https://doi.org/10.1002/ajb2.16177openalex-snapshot
Beyond pollen:ovule ratios: Evolutionary consequences of pollinator dependence and pollination efficiency for pollen and ovule production in angiosperms
inferredcites →https://doi.org/10.1002/ajb2.16180openalex-snapshot
Pollen production per flower increases with floral display size across animal‐pollinated flowering plants
inferredcites →https://doi.org/10.1002/ajb2.16197openalex-snapshot
Ploidy effects on the relationship between floral phenotype, reproductive investment, and fitness in an autogamous species complex
inferredcites →https://doi.org/10.1002/cyto.a.24495openalex-snapshot
Reference standards for flow cytometric estimation of absolute nuclear DNA content in plants
inferredcites →https://doi.org/10.1002/j.1537-2197.1940.tb13952.xopenalex-snapshot
DEMONSTRATION OF THE THREE GERM LAYERS IN THE SHOOT APEX OF DATURA BY MEANS OF INDUCED POLYPLOIDY IN PERICLINAL CHIMERAS
inferredcites →https://doi.org/10.1002/j.1537-2197.1948.tb08143.xopenalex-snapshot
CYTOLOGICAL AND GROWTH CORRELATIONS IN THE FLOWER BUD AND ANTHER OF LILIUM LONGIFLORUM
inferredcites →https://doi.org/10.1002/j.1537-2197.1980.tb07680.xopenalex-snapshot
INTRA‐INFLORESCENCE VARIABILITY IN POLLEN/OVULE RATIOS IN THE CLEISTOGAMOUS SPECIES LAMIUM AMPLEXICAULE (LABIATAE)
inferredcites →https://doi.org/10.1002/j.1537-2197.1992.tb13752.xopenalex-snapshot
THE EFFECTS OF GENOTYPE AND PLOIDY LEVEL ON POLLEN SURFACE SCULPTURING IN MAIZE (ZEA MAYS L.)
inferredcites →https://doi.org/10.1006/anbo.1998.0730openalex-snapshot
Plant Genome Size Estimation by Flow Cytometry: Inter-laboratory Comparison*1
inferredcites →https://doi.org/10.1007/bf00232939openalex-snapshot
Easy determination of ploidy level in Arabidopsis thaliana plants by means of pollen size measurement
inferredcites →https://doi.org/10.1007/bf00985263openalex-snapshot
Variation of pollen and ovule parameters among different ploidy levels ofCorydalis (Fumariaceae)
inferredcites →https://doi.org/10.1007/bf02860830openalex-snapshot
On Ö. Winge and a Prayer: The origins of polyploidy
inferredcites →https://doi.org/10.1007/s00497-021-00426-zopenalex-snapshot
Consequences of whole genome duplication for 2n pollen performance
inferredcites →https://doi.org/10.1007/s00497-022-00448-1openalex-snapshot
Learning to tango with four (or more): the molecular basis of adaptation to polyploid meiosis
inferredcites →https://doi.org/10.1007/s10265-022-01373-0openalex-snapshot
Higher frequency of legitimate pollinators and fruit set of autotetraploid trees of Libidibia ferrea (Leguminosae) compared to diploids in a mixed tropical urban population
inferredcites →https://doi.org/10.1016/j.pbi.2014.05.008openalex-snapshot
Dosage, duplication, and diploidization: clarifying the interplay of multiple models for duplicate gene evolution over time
inferredcites →https://doi.org/10.1016/j.ppees.2025.125872openalex-snapshot
Untangling the relationship between pollination efficiency and pollen-ovule ratios
inferredcites →https://doi.org/10.1017/s1464793106007007openalex-snapshot
Bivariate line‐fitting methods for allometry
inferredcites →https://doi.org/10.1038/s41559-018-0787-9openalex-snapshot
The global biogeography of polyploid plants
inferredcites →https://doi.org/10.1073/pnas.1910631117openalex-snapshot
The maleness of larger angiosperm flowers
inferredcites →https://doi.org/10.1080/0028825x.1979.10432573openalex-snapshot
Parental strategies of angiosperms
inferredcites →https://doi.org/10.1086/284115openalex-snapshot
Polyploidy and Novelty in Flowering Plants
inferredcites →https://doi.org/10.1086/332991openalex-snapshot
Developmental Selection in Vascular Plants
inferredcites →https://doi.org/10.1086/336193openalex-snapshot
Studies of Floral Morphology in the Ericales VI. The Diapensiaceae
inferredcites →https://doi.org/10.1086/376813openalex-snapshot
Habitat Differentiation between Diploid and Tetraploid Galax urceolata (Diapensiaceae)
inferredcites →https://doi.org/10.1086/523367openalex-snapshot
Mating Consequences of Polyploid Evolution in Flowering Plants: Current Trends and Insights from Synthetic Polyploids
inferredcites →https://doi.org/10.1086/700636openalex-snapshot
Polyploidy, the Nucleotype, and Novelty: The Impact of Genome Doubling on the Biology of the Cell
inferredcites →https://doi.org/10.1093/aob/mcaa007openalex-snapshot
For things to stay the same, things must change: polyploidy and pollen tube growth rates
inferredcites →https://doi.org/10.1093/aob/mci245openalex-snapshot
Polyploidy and Cellular Mechanisms Changing Leaf Size: Comparison of Diploid and Autotetraploid Populations in Two Species of Lolium
inferredcites →https://doi.org/10.1093/aob/mcn038openalex-snapshot
A Strong Nucleotypic Effect on the Cell Cycle Regardless of Ploidy Level
inferredcites →https://doi.org/10.1093/aob/mcr023openalex-snapshot
The selfing syndrome: a model for studying the genetic and evolutionary basis of morphological adaptation in plants
inferredcites →https://doi.org/10.1093/aob/mcr120openalex-snapshot
Angiosperm ovules: diversity, development, evolution
inferredcites →https://doi.org/10.1093/aob/mcr267openalex-snapshot
Genome size and DNA base composition of geophytes: the mirror of phenology and ecology?
inferredcites →https://doi.org/10.1093/jxb/erv432openalex-snapshot
Whole genome duplications in plants: an overview fromArabidopsis
inferredcites →https://doi.org/10.1093/molbev/msab096openalex-snapshot
Novelty and Convergence in Adaptation to Whole Genome Duplication
inferredcites →https://doi.org/10.1093/oxfordjournals.jhered.a105053openalex-snapshot
GALAX: THE GENUS AND ITS CHROMOSOMES
inferredcites →https://doi.org/10.1093/plcell/koac287openalex-snapshot
Anther development—The long road to making pollen
inferredcites →https://doi.org/10.1098/rspb.1971.0066openalex-snapshot
The duration of meiosis
inferredcites →https://doi.org/10.1098/rspb.1972.0041openalex-snapshot
The effects of polyploidy on meiotic duration and pollen development in cereal anthers
inferredcites →https://doi.org/10.1098/rspb.2002.2196openalex-snapshot
Pollen competition as a unilateral reproductive barrier between sympatric diploid and tetraploidChamerion angustifolium
inferredcites →https://doi.org/10.1098/rspb.2010.2208openalex-snapshot
Genome duplication and the evolution of conspecific pollen precedence
inferredcites →https://doi.org/10.1098/rstb.2013.0352openalex-snapshot
Ecological studies of polyploidy in the 100 years following its discovery
inferredcites →https://doi.org/10.1098/rstb.2020.0510openalex-snapshot
The selfing syndrome and beyond: diverse evolutionary consequences of mating system transitions in plants
inferredcites →https://doi.org/10.1104/pp.18.00967openalex-snapshot
Polyploidy Affects Plant Growth and Alters Cell Wall Composition
inferredcites →https://doi.org/10.1105/tpc.110.076133openalex-snapshot
Heterosis
inferredcites →https://doi.org/10.1105/tpc.18.00344openalex-snapshot
Ploidy and Size at Multiple Scales in the Arabidopsis Sepal
inferredcites →https://doi.org/10.1111/geb.13469openalex-snapshot
Increasing pollen production at high latitudes across animal‐pollinated flowering plants
inferredcites →https://doi.org/10.1111/j.1420-9101.2010.02057.xopenalex-snapshot
Spatial seed and pollen games: dispersal, sex allocation, and the evolution of dioecy
inferredcites →https://doi.org/10.1111/j.1469-8137.2009.03043.xopenalex-snapshot
Correlated evolution of mating system and floral display traits in flowering plants and its implications for the distribution of mating system variation
inferredcites →https://doi.org/10.1111/j.1469-8137.2011.03932.xopenalex-snapshot
A piece of the puzzle: a method for comparing pollination quality and quantity across multiple species and reproductive events
inferredcites →https://doi.org/10.1111/j.1558-5646.1984.tb00383.xopenalex-snapshot
POLLEN-OVULE RATIOS AND HERMAPHRODITE SEXUAL ALLOCATION STRATEGIES
inferredcites →https://doi.org/10.1111/j.1558-5646.1995.tb05962.xopenalex-snapshot
OVULE PACKAGING IN STOCHASTIC POLLINATION AND FERTILIZATION ENVIRONMENTS
inferredcites →https://doi.org/10.1111/j.1601-5223.1936.tb03204.xopenalex-snapshot
The Evolutionary Significance of Autopolyploidy
inferredcites →https://doi.org/10.1111/j.1744-7348.1970.tb04610.xopenalex-snapshot
Pollen release by diploid and tetraploid sugar‐beet plants
inferredcites →https://doi.org/10.1111/jeb.12986openalex-snapshot
Ordinary least squares regression is indicated for studies of allometry
inferredcites →https://doi.org/10.1111/jipb.13314openalex-snapshot
Ovule initiation: the essential step controlling offspring number in Arabidopsis
inferredcites →https://doi.org/10.1111/nph.12184openalex-snapshot
Sexual polyploidization in plants – cytological mechanisms and molecular regulation
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.13499openalex-snapshot
Meiosis evolves: adaptation to external and internal environments
inferredcites →https://doi.org/10.1111/nph.13750openalex-snapshot
Does an ‘oversupply’ of ovules cause pollen limitation?
inferredcites →https://doi.org/10.1111/nph.13881openalex-snapshot
Genome size and ploidy influence angiosperm species' biomass under nitrogen and phosphorus limitation
inferredcites →https://doi.org/10.1111/nph.19929openalex-snapshot
Pollination efficiency and the pollen–ovule ratio
inferredcites →https://doi.org/10.1111/oik.10267openalex-snapshot
Polyploidy‐induced floral changes lead to unexpected pollinator behavior in Arabidopsis arenosa
inferredcites →https://doi.org/10.1126/science.adh0755openalex-snapshot
Defective pollen tube tip growth induces neo-polyploid infertility
inferredcites →https://doi.org/10.1139/g72-063openalex-snapshot
THE DURATION OF MEIOSIS IN DIPLOID AND AUTOTETRAPLOID BARLEY
inferredcites →https://doi.org/10.1146/annurev.ecolsys.33.010802.150437openalex-snapshot
Neopolyploidy in Flowering Plants
inferredcites →https://doi.org/10.1186/s13059-020-1935-5openalex-snapshot
Opportunities and challenges in long-read sequencing data analysis
inferredcites →https://doi.org/10.1242/dev.196618openalex-snapshot
Asynchrony of ovule primordia initiation in Arabidopsis
inferredcites →https://doi.org/10.1371/journal.pone.0083729openalex-snapshot
Does Ploidy Level Directly Control Cell Size? Counterevidence from Arabidopsis Genetics
inferredcites →https://doi.org/10.1508/cytologia.52.309openalex-snapshot
Cell volume ratios of natural and of induced tetraploid and diploid flowering plants.
inferredcites →https://doi.org/10.1674/0003-0031-177.2.299openalex-snapshot
The Reproductive Ecology of Diploid and Tetraploid Galax urceolata
inferredcites →https://doi.org/10.1890/06-1017openalex-snapshot
EXPANDING THE LIMITS OF THE POLLEN-LIMITATION CONCEPT: EFFECTS OF POLLEN QUANTITY AND QUALITY
inferredcites →https://doi.org/10.21273/jashs05376-24openalex-snapshot
Flow Cytometry for Estimating Plant Genome Size: Revisiting Assumptions, Sources of Variation, Reference Standards, and Best Practices
inferredcites →https://doi.org/10.2307/1218997openalex-snapshot
MINORITY CYTOTYPE EXCLUSION IN LOCAL PLANT POPULATIONS
inferredcites →https://doi.org/10.2307/2389709openalex-snapshot
Allocations to Pollen, Seeds and Pollination Mechanisms in Self-Fertilizing Plants
inferredcites →https://doi.org/10.2307/2398913openalex-snapshot
Form and Function in Angiosperm Pollen
inferredcites →https://doi.org/10.2307/2407542openalex-snapshot
Pollen-Ovule Ratios: A Conservative Indicator of Breeding Systems in Flowering Plants
inferredcites →https://doi.org/10.2307/2418558openalex-snapshot
Flavonoid Chemistry of Cytotypes in Galax (Diapensiaceae)
inferredcites →https://doi.org/10.2307/2445530openalex-snapshot
Size-Number Trade-Offs and Pollen Production by Papilionaceous Legumes
inferredcites →https://doi.org/10.3390/plants11131647openalex-snapshot
Developmental Differences between Anthers of Diploid and Autotetraploid Rice at Meiosis
inferredcites →https://doi.org/10.3732/ajb.0800183openalex-snapshot
Ovule number per flower in a world of unpredictable pollination
inferredcites →https://doi.org/10.3732/ajb.1400554openalex-snapshot
Population genetic variation, geographic structure, and multiple origins of autopolyploidy in Galax urceolata
inferredcites →https://doi.org/10.3732/ajb.1600183openalex-snapshot
The role of polyploidy in shaping morphological diversity in natural populations of Phlox amabilis
inferredcites →https://doi.org/10.3732/ajb.94.9.1527openalex-snapshot
Polyploidy and self‐fertilization in flowering plants
inferredcites →https://doi.org/10.5962/p.185365openalex-snapshot
Stomata Size and Distribution in Diploid and Polyploid Plants
inferredcites →https://doi.org/10.7312/steb94536openalex-snapshot
Variation and Evolution in Plants
Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.