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Ploidy dimorphism and reproductive biology inStenodrepanum bergii(Leguminosae), a rare South American endemism
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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.1537-2197.1988.tb11268.xopenalex-snapshot
REPRODUCTIVE BIOLOGY OF DIPLOID AND TRIPLOID APIOS AMERICANA (LEGUMINOSAE)
inferredcites →https://doi.org/10.1002/j.1537-2197.1992.tb13725.xopenalex-snapshot
LOCAL POLYPLOID VARIATION IN THE NATIVE PRAIRIE GRASS ANDROPOGON GERARDII
inferredcites →https://doi.org/10.1007/bf00935987openalex-snapshot
Phylogenetic relationships and gene flow between sympatric diploid and tetraploid plants ofDactylis glomerata (Gramineae)
inferredcites →https://doi.org/10.1007/bf02860830openalex-snapshot
On Ö. Winge and a Prayer: The origins of polyploidy
inferredcites →https://doi.org/10.1016/s0006-3207(02)00312-9openalex-snapshot
Genetic variation in the endangered Inner Mongolia endemic shrub Tetraena mongolica Maxim. (Zygophyllaceae)
inferredcites →https://doi.org/10.1038/nrg1711openalex-snapshot
The advantages and disadvantages of being polyploid
inferredcites →https://doi.org/10.1046/j.1095-8339.2003.00116.xopenalex-snapshot
Cytotypes of Andropogon gerardii Vitman (Poaceae): fertility and reproduction of aneuploids
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a026092openalex-snapshot
Phylogenetic relationships among ascomycetes: evidence from an RNA polymerse II subunit
inferredcites →https://doi.org/10.1111/j.0014-3820.2004.tb01645.xopenalex-snapshot
EVOLUTION OF TRIPLOIDY IN APIOS AMERICANA (LEGUMINOSAE) REVEALED BY GENEALOGICAL ANALYSIS OF THE HISTONE H3-D GENE
inferredcites →https://doi.org/10.1139/b76-276openalex-snapshot
Studies on the genus Apios. I. Chromosome number and distribution of Apios americana and A. priceana
inferredcites →https://doi.org/10.1139/g87-056openalex-snapshot
Permanent odd polyploidy in a grass ( Andropogon ternatus )
inferredcites →https://doi.org/10.1139/g90-015openalex-snapshot
Distribution of polyploid variation in big bluestem (Andropogon gerardii, Poaceae) across the tallgrass prairie region
inferredcites →https://doi.org/10.1146/annurev.ecolsys.29.1.467openalex-snapshot
PATHWAYS, MECHANISMS, AND RATES OF POLYPLOID FORMATION IN FLOWERING PLANTS
inferredcites →https://doi.org/10.2307/2446081openalex-snapshot
Evolutionary implications of meiotic Chromosome Behavior, Reproductive Biology, and Hybridization in 6X and 9X Cytotypes of Andropogon gerardii (Poaceae)
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.3897/phytokeys.240.101716zenodo-depositor-declared
Advances in Legume Systematics 14. Classification of Caesalpinioideae. Part 2: Higher-level classification
inferred← citeshttps://doi.org/10.1002/tax.614006openalex-snapshot
The phylogenetic relationships of four monospecific caesalpinioids (Leguminosae) endemic to southern South America
inferred← citeshttps://doi.org/10.1007/7397_2015_17openalex-snapshot
Phylogeny and Evolution of the Genus Brachypodium
inferred← citeshttps://doi.org/10.1007/s00425-016-2472-zopenalex-snapshot
Characterization of wheat-Secale africanum chromosome 5Ra derivatives carrying Secale specific genes for grain hardness
inferred← citeshttps://doi.org/10.1007/s00438-014-0825-5openalex-snapshot
What does the nr5S DNA multigene family tell us about the genomic relationship between Dasypyrum breviaristatum and D. villosum (Triticeae: Poaceae)?
inferred← citeshttps://doi.org/10.1007/s00438-014-0907-4openalex-snapshot
Diversity within the genus Elymus (Poaceae: Triticeae) as investigated by the analysis of the nr5S rDNA variation in species with St and H haplomes
inferred← citeshttps://doi.org/10.1007/s00438-015-1096-5openalex-snapshot
Diversity within the genus Elymus (Poaceae: Triticeae) II: analyses of variation within 5S nrDNA restrict membership in the genus to species with StH genomes
inferred← citeshttps://doi.org/10.1007/s10722-017-0519-zopenalex-snapshot
Lophopyrum Á. Löve (1980), Thinopyrum Á. Löve (1980), Trichopyrum Á. Löve (1986): one, two or three genera? A study based on the nuclear 5S DNA
inferred← citeshttps://doi.org/10.1007/s11032-016-0574-8openalex-snapshot
Thai jasmine rice cultivar KDML105 carrying Saltol QTL exhibiting salinity tolerance at seedling stage
inferred← citeshttps://doi.org/10.1007/s11105-019-01138-5openalex-snapshot
Application of High-Throughput Sequencing to Evaluate the Genetic Diversity Among Wild Apple Species Indigenous to Shandong, China, and Introduced Cultivars
inferred← citeshttps://doi.org/10.1007/s13258-013-0056-xopenalex-snapshot
Evolution of plant Ash1 SET genes: structural divergence and functional differentiation
inferred← citeshttps://doi.org/10.1016/j.actatropica.2015.05.015openalex-snapshot
Simulium ( Gomphostilbia ) (Diptera: Simuliidae) from Southern Western Ghats, India: Two new species and DNA barcoding
inferred← citeshttps://doi.org/10.1016/j.bse.2014.04.017openalex-snapshot
Isozyme variation and differentiation of morphologically cryptic species in the Brachypodium distachyon complex
inferred← citeshttps://doi.org/10.1016/j.flora.2024.152519openalex-snapshot
Facing climate change: Range dynamics and chromosome diversity in Hedeoma multiflora Benth., a South American aromatic-medicinal plant at risk
inferred← citeshttps://doi.org/10.1016/j.ppees.2017.11.004openalex-snapshot
Heterochromatic and cytomolecular diversification in the Caesalpinia group (Leguminosae): Relationships between phylogenetic and cytogeographical data
inferred← citeshttps://doi.org/10.1016/j.ppees.2019.03.002openalex-snapshot
Do tropical plants have smaller genomes? Correlation between genome size and climatic variables in the Caesalpinia Group (Caesalpinioideae, Leguminosae)
inferred← citeshttps://doi.org/10.1071/bt14229openalex-snapshot
Causes of infertility in the endangered Australian endemic plant Borya mirabilis (Boryaceae)
inferred← citeshttps://doi.org/10.1080/00087114.2013.829690openalex-snapshot
Genome size variation and evolution in the family Asteraceae
inferred← citeshttps://doi.org/10.1111/pbr.12321openalex-snapshot
Identification of salt tolerance‐improving quantitative trait loci alleles from a salt‐susceptible rice breeding line by introgression breeding
inferred← citeshttps://doi.org/10.1371/journal.pone.0051058openalex-snapshot
A DNA Barcoding Method to Discriminate between the Model Plant Brachypodium distachyon and Its Close Relatives B. stacei and B. hybridum (Poaceae)
inferred← citeshttps://doi.org/10.1600/036364417x696005openalex-snapshot
A New Allopolyploid Species of Saccharum (Poaceae ‐ Andropogoneae) from South America, with Notes on its Cytogenetics
inferred← citeshttps://doi.org/10.3389/fpls.2017.00041openalex-snapshot
Marker Aided Incorporation of Saltol, a Major QTL Associated with Seedling Stage Salt Tolerance, into Oryza sativa ‘Pusa Basmati 1121’
inferred← citeshttps://doi.org/10.3389/fpls.2018.01460openalex-snapshot
Genetic Characterization of the Apple Germplasm Collection in Central Italy: The Value of Local Varieties
inferred← citeshttps://doi.org/10.3897/phytokeys.71.9203openalex-snapshot
A new generic system for the pantropical Caesalpinia group (Leguminosae)
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