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Phylogenetic relationships of Aristida and relatives (Poaceae, Aristidoideae) based on noncoding chloroplast (trnL‐F, rpl16) and nuclear (ITS) DNA sequences
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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/fedr.19931040511openalex-snapshot
Leaf anatomical studies and its bearing on the taxonomy of the tribe Aristideae (Poaceae) from Nigeria With 6 Figures and one Table
inferredcites →https://doi.org/10.1002/j.1537-2197.1958.tb10608.xopenalex-snapshot
CHROMOSOME NUMBERS IN SOUTHWESTERN GRASSE
inferredcites →https://doi.org/10.1002/j.1537-2197.1977.tb07611.xopenalex-snapshot
CHROMOSOME NUMBERS IN WESTERN GRASSES
inferredcites →https://doi.org/10.1002/j.1537-2197.1985.tb08293.xopenalex-snapshot
DIFFERING ONTOGENETIC ORIGINS OF PCR (“KRANZ”) SHEATHS IN LEAF BLADES OF C4 GRASSES (POACEAE)
inferredcites →https://doi.org/10.1002/j.1537-2197.1996.tb12724.xopenalex-snapshot
Low Levels of Intraspecific Genetic Variation at a Rapidly Evolving Chloroplast DNA Locus in North American Duckweeds (Lemnaceae)
inferredcites →https://doi.org/10.1002/j.1537-2197.1996.tb13940.xopenalex-snapshot
Parallelism and diversity in multiple origins of c4 photosynthesis in the grass family
inferredcites →https://doi.org/10.1002/tax.583015openalex-snapshot
Globally grown, but poorly known: species limits and biogeography of Gazania Gaertn. (Asteraceae) inferred from chloroplast and nuclear DNA sequence data
inferredcites →https://doi.org/10.1002/tax.604014openalex-snapshot
Centropodieae and Ellisochloa , a new tribe and genus in Chloridoideae (Poaceae)
inferredcites →https://doi.org/10.1006/mpev.1997.0432openalex-snapshot
Molecular Evolution and Phylogenetic Utility of the Chloroplastrpl16Intron inChusqueaand the Bambusoideae (Poaceae)
inferredcites →https://doi.org/10.1006/mpev.2000.0845openalex-snapshot
Noise and Incongruence: Interpreting Results of the Incongruence Length Difference Test
inferredcites →https://doi.org/10.1007/bf00037152openalex-snapshot
Universal primers for amplification of three non-coding regions of chloroplast DNA
inferredcites →https://doi.org/10.1007/bf00226978openalex-snapshot
Phylogenetic analysis of Sorghum and related taxa using internal transcribed spacers of nuclear ribosomal DNA
inferredcites →https://doi.org/10.1007/bf00388331openalex-snapshot
Biochemical and cytological relationships in C4 plants
inferredcites →https://doi.org/10.1007/bf01287454openalex-snapshot
Occurrence of the suberized lamella in leaves of grasses of different photosynthetic types. I. In parenchymatous bundle sheaths and PCR (?Kranz?) sheaths
inferredcites →https://doi.org/10.1007/bf02868851openalex-snapshot
Phylogenetics and character evolution in the grass family (Poaceae): Simultaneous analysis of morphological and Chloroplast DNA restriction site character sets
inferredcites →https://doi.org/10.1007/s10592-005-9073-xopenalex-snapshot
Development and characterization of polymorphic microsatellite loci in endangered fern Adiantum reniforme var. sinense
inferredcites →https://doi.org/10.1016/0031-0182(79)90071-3openalex-snapshot
Geo- and biodynamic effects of the Messinian salinity crisis in the Mediterranean
inferredcites →https://doi.org/10.1016/0031-0182(79)90082-8openalex-snapshot
Geo- and biodynamic effects of the Messinian salinity crisis in the Mediterranean
inferredcites →https://doi.org/10.1016/0031-0182(90)90178-aopenalex-snapshot
Neogene stratigraphy, paleoceanography and paleobiogeography in northwest South America and the evolution of the Panama seaway
inferredcites →https://doi.org/10.1016/0031-9422(80)85004-7openalex-snapshot
Deviations from michaelis-menten behaviour of plant glutamate dehydrogenase with ammonium as variable substrate
inferredcites →https://doi.org/10.1016/0968-0004(90)90252-7openalex-snapshot
PCR protocols — A guide to methods and applications
inferredcites →https://doi.org/10.1016/b978-0-12-372180-8.50042-1openalex-snapshot
AMPLIFICATION AND DIRECT SEQUENCING OF FUNGAL RIBOSOMAL RNA GENES FOR PHYLOGENETICS
inferredcites →https://doi.org/10.1016/b978-0-12-715007-9.50014-1openalex-snapshot
tRNAs and tRNA Genes of Plastids
inferredcites →https://doi.org/10.1016/b978-012614440-6/50006-9openalex-snapshot
Leaf Structure and Development in C4 Plants
inferredcites →https://doi.org/10.1016/b978-012614440-6/50017-3openalex-snapshot
The Taxonomic Distribution of C4 Photosynthesis
inferredcites →https://doi.org/10.1016/j.cub.2007.11.058openalex-snapshot
Oligocene CO2 Decline Promoted C4 Photosynthesis in Grasses
inferredcites →https://doi.org/10.1016/j.earscirev.2011.02.002openalex-snapshot
Regional and global context of the Late Cenozoic Langebaanweg (LBW) palaeontological site: West Coast of South Africa
inferredcites →https://doi.org/10.1016/j.plantsci.2004.10.005openalex-snapshot
Evidence that C4 species in genus Stipagrostis, family Poaceae, are NADP-malic enzyme subtype with nonclassical type of Kranz anatomy (Stipagrostoid)
inferredcites →https://doi.org/10.1016/j.sajb.2010.12.003openalex-snapshot
A new species of Sartidia (Graminae), endemic to ultramafic soils
inferredcites →https://doi.org/10.1016/j.tig.2003.12.003openalex-snapshot
Reading the entrails of chickens: molecular timescales of evolution and the illusion of precision
inferredcites →https://doi.org/10.1016/j.tplants.2005.09.006openalex-snapshot
Evolution of diversity: the Cape flora
inferredcites →https://doi.org/10.1016/j.ympev.2003.12.006openalex-snapshot
PRAP—computation of Bremer support for large data sets
inferredcites →https://doi.org/10.1016/j.ympev.2008.01.035openalex-snapshot
Large multi-gene phylogenetic trees of the grasses (Poaceae): Progress towards complete tribal and generic level sampling
inferredcites →https://doi.org/10.1016/j.ympev.2010.07.019openalex-snapshot
The evolutionary history and biogeography of Mimosoideae (Leguminosae): An emphasis on African acacias
inferredcites →https://doi.org/10.1016/s0021-9258(20)81919-xopenalex-snapshot
Nucleotide sequences of five maize chloroplast transfer RNA genes and their flanking regions.
inferredcites →https://doi.org/10.1017/s1464793103006171openalex-snapshot
The radiation of the Cape flora, southern Africa
inferredcites →https://doi.org/10.1023/a:1018325026863openalex-snapshot
Floristic biodiversity and history of African arid regions
inferredcites →https://doi.org/10.1071/bru9800271openalex-snapshot
Aristida L. (Poaceae, Aristideae) in Australia.
inferredcites →https://doi.org/10.1071/fp04118openalex-snapshot
Functional compartmentation of C4 photosynthesis in the triple layered chlorenchyma of Aristida (Poaceae)
inferredcites →https://doi.org/10.1071/pp9770523openalex-snapshot
In situ Immunofluorescent Labelling of Ribulose-1,5-Bisphosphate Carboxylase in Leaves of C3 and C4 Plants
inferredcites →https://doi.org/10.1071/pp9870403openalex-snapshot
New Structural/Biochemical Associations in Leaf Blades of C4 Grasses (Poaceae)
inferredcites →https://doi.org/10.1071/sb06020openalex-snapshot
Multiple sequence alignment for phylogenetic purposes
inferredcites →https://doi.org/10.1071/sb97001openalex-snapshot
A molecular phylogeny of the subfamily Arundinoideae (Poaceae) based on sequences of rDNA
inferredcites →https://doi.org/10.1071/sb97012openalex-snapshot
A molecular phylogeny of the grass family (Poaceae) based on the sequences of nuclear ribosomal DNA (ITS)
inferredcites →https://doi.org/10.1071/sb9920129openalex-snapshot
A revision of the genus Aristida (Poaceae) in Australia
inferredcites →https://doi.org/10.1080/10635150290102456openalex-snapshot
Divergence Time and Evolutionary Rate Estimation with Multilocus Data
inferredcites →https://doi.org/10.1080/10635150490264752openalex-snapshot
Congruence Versus Phylogenetic Accuracy: Revisiting the Incongruence Length Difference Test
inferredcites →https://doi.org/10.1093/aob/mcr213openalex-snapshot
Diversity, phylogeny, and evolution in the monocotyledons
inferredcites →https://doi.org/10.1093/bioinformatics/14.9.817openalex-snapshot
MODELTEST: testing the model of DNA substitution.
inferredcites →https://doi.org/10.1093/bioinformatics/btg180openalex-snapshot
MrBayes 3: Bayesian phylogenetic inference under mixed models
inferredcites →https://doi.org/10.1093/bioinformatics/btg427openalex-snapshot
Parallel Metropolis coupled Markov chain Monte Carlo for Bayesian phylogenetic inference
inferredcites →https://doi.org/10.1093/jxb/err048openalex-snapshot
The C4 plant lineages of planet Earth
inferredcites →https://doi.org/10.1093/molbev/msg190openalex-snapshot
Patterns and Relative Rates of Nucleotide and Insertion/Deletion Evolution at Six Chloroplast Intergenic Regions in New World Species of the Lecythidaceae
inferredcites →https://doi.org/10.1093/nar/13.21.7543openalex-snapshot
Chloroplast promoters from higher plants
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a025677openalex-snapshot
The phytochrome gene family in grasses (Poaceae): a phylogeny and evidence that grasses have a subset of the loci found in dicot angiosperms
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a025811openalex-snapshot
Bayesian phylogenetic inference using DNA sequences: a Markov Chain Monte Carlo Method
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a026043openalex-snapshot
Molecular evolution of a tandemly repeated trnF(GAA) gene in the chloroplast genomes of Microseris (Asteraceae) and the use of structural mutations in phylogenetic analyses
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040082openalex-snapshot
Maximum-likelihood estimation of phylogeny from DNA sequences when substitution rates differ over sites.
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040442openalex-snapshot
Slipped-strand mispairing: a major mechanism for DNA sequence evolution.
inferredcites →https://doi.org/10.1093/sysbio/18.1.1openalex-snapshot
Quantitative Phyletics and the Evolution of Anurans
inferredcites →https://doi.org/10.1093/sysbio/22.3.240openalex-snapshot
Maximum Likelihood and Minimum-Steps Methods for Estimating Evolutionary Trees from Data on Discrete Characters
inferredcites →https://doi.org/10.1093/sysbio/syp035openalex-snapshot
Accounting for Calibration Uncertainty in Phylogenetic Estimation of Evolutionary Divergence Times
inferredcites →https://doi.org/10.1098/rstb.2004.1533openalex-snapshot
Palaeobotanical studies from tropical Africa: relevance to the evolution of forest, woodland and savannah biomes
inferredcites →https://doi.org/10.1098/rstb.2008.0075openalex-snapshot
Plant species radiations: where, when, why?
inferredcites →https://doi.org/10.1111/j.1095-8339.2010.01041.xopenalex-snapshot
Biogeography of the grasses (Poaceae): a phylogenetic approach to reveal evolutionary history in geographical space and geological time
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.1096-0031.1994.tb00181.xopenalex-snapshot
TESTING SIGNIFICANCE OF INCONGRUENCE
inferredcites →https://doi.org/10.1111/j.1096-0031.1999.tb00277.xopenalex-snapshot
The Parsimony Ratchet, a New Method for Rapid Parsimony Analysis
inferredcites →https://doi.org/10.1111/j.1365-2486.2008.01688.xopenalex-snapshot
The age of the grasses and clusters of origins of C4 photosynthesis
inferredcites →https://doi.org/10.1111/j.1365-2486.2009.01860.xopenalex-snapshot
The origins and diversification of C4 grasses and savanna‐adapted ungulates
inferredcites →https://doi.org/10.1111/j.1399-3054.1992.tb04722.xopenalex-snapshot
Immunogold localization of photosynthetic enzymes in leaves of Aristida latifolia, a unique C4 grass with a double chlorenchymatous bundle sheath
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.1601-5223.1983.tb00895.xopenalex-snapshot
Interspecific hybridization with cultivated barley (Hordeum vulgare L.)
inferredcites →https://doi.org/10.1146/annurev.es.26.110195.003301openalex-snapshot
SEPARATE VERSUS COMBINED ANALYSIS OF PHYLOGENETIC EVIDENCE
inferredcites →https://doi.org/10.1186/1471-2148-7-214openalex-snapshot
BEAST: Bayesian evolutionary analysis by sampling trees
inferredcites →https://doi.org/10.1371/journal.pbio.0040088openalex-snapshot
Relaxed Phylogenetics and Dating with Confidence
inferredcites →https://doi.org/10.1600/036364407780360102openalex-snapshot
Reinstatement and Emendation of Subfamily Micrairoideae (Poaceae)
inferredcites →https://doi.org/10.2307/1222917openalex-snapshot
Electrophoreíic and immunological studies of prolamins in the Poaceae: II. Phylogenetic affinities of the Aristideae
inferredcites →https://doi.org/10.2307/1222975openalex-snapshot
Silica gel: An ideal material for field preservation of leaf samples for DNA studies
inferredcites →https://doi.org/10.2307/1223934openalex-snapshot
An improved method of DNA isolation from plants collected in the field and conserved in saturated NaCl/CTAB solution
inferredcites →https://doi.org/10.2307/2399681openalex-snapshot
A Method for Collecting Dried Plant Specimens for DNA and Isozyme Analyses, and the Results of a Field Test in Xinjiang, China
inferredcites →https://doi.org/10.2307/2399839openalex-snapshot
Numeros Cromosomicos de Algunas Especies Mexicanas de Aristida (Poaceae: Aristideae)
inferredcites →https://doi.org/10.2307/2399851openalex-snapshot
Phylogenetic Relationships Among Members of Saxifragaceae Sensu Lato Based on rbcL Sequence Data
inferredcites →https://doi.org/10.2307/2412304openalex-snapshot
Maximum Likelihood and Minimum-Steps Methods for Estimating Evolutionary Trees from Data on Discrete Characters
inferredcites →https://doi.org/10.2307/2412407openalex-snapshot
Quantitative Phyletics and the Evolution of Anurans
inferredcites →https://doi.org/10.2307/2419509openalex-snapshot
Sequences of the Grass-Specific Insert in the Chloroplast rpoC2 Gene Elucidate Generic Relationships of the Arundinoideae (Poaceae)
inferredcites →https://doi.org/10.2307/2419802openalex-snapshot
Polyphyly of Arundinoideae (Poaceae): Evidence from rbcL Sequence Data
inferredcites →https://doi.org/10.2307/2419803openalex-snapshot
A Phylogeny of the Grass Family (Poaceae) Based on ndhF Sequence Data
inferredcites →https://doi.org/10.2307/2656688openalex-snapshot
Phylogenetic structure in the grass family (Poaceae): evidence from the nuclear gene phytochrome B
inferredcites →https://doi.org/10.2307/2666171openalex-snapshot
Phylogeny of Poaceae Inferred from matK Sequences
inferredcites →https://doi.org/10.2307/2666185openalex-snapshot
The History of Neotropical Vegetation: New Developments and Status
inferredcites →https://doi.org/10.2307/2666186openalex-snapshot
The Origin of Grass-Dominated Ecosystems
inferredcites →https://doi.org/10.2307/2807332openalex-snapshot
Genera Graminum. Grasses of the World.
inferredcites →https://doi.org/10.2307/2807694openalex-snapshot
The Aristida pansa Complex and a Key to the Divaricatae Group of North America (Gramineae: Aristideae)
inferredcites →https://doi.org/10.2307/3298585openalex-snapshot
Phylogeny and Subfamilial Classification of the Grasses (Poaceae)
inferredcites →https://doi.org/10.2307/3669912openalex-snapshot
Chromosome Numbers in the Aristida purpurea Complex (Gramineae)
inferredcites →https://doi.org/10.2307/4114451openalex-snapshot
Genera Graminum. Grasses of the World
inferredcites →https://doi.org/10.3372/wi.38.38108openalex-snapshot
The genera Aristida and Stipagrostis (Poaceae) in Iran
inferredcites →https://doi.org/10.3732/ajb.0800185openalex-snapshot
Phylogeny of the tribe Indigofereae (Leguminosae–Papilionoideae): Geographically structured more in succulent‐rich and temperate settings than in grass‐rich environments
inferredcites →https://doi.org/10.3732/ajb.0800265openalex-snapshot
C3 photosynthesis in Aristida longifolia: Implication for photosynthetic diversification in Aristidoideae (Poaceae)
inferredcites →https://doi.org/10.3732/ajb.0900111openalex-snapshot
Two independent C 4 origins in Aristidoideae (Poaceae) revealed by the recruitment of distinct phosphoenolpyruvate carboxylase genes
inferredcites →https://doi.org/10.3732/ajb.0900229openalex-snapshot
Biogeography of Cedrela (Meliaceae, Sapindales) in Central and South America
inferredcites →https://doi.org/10.3732/ajb.1000339openalex-snapshot
Old-New World and trans-African disjunctions of Thamnosma (Rutaceae): Intercontinental long-distance dispersal and local differentiation in the succulent biome
inferredcites →https://doi.org/10.4102/abc.v4i1.1713openalex-snapshot
AN ACCOUNT OF THE SOUTH AFRICAN MATERIAL OF ARISTIDA LINN: IN CERTAIN EUROPEAN AND SOUTH AFRICAN HERBARIA.
inferredcites →https://doi.org/10.5281/zenodo.16238161openalex-snapshot
The Kranz syndrome and its subtypes in grass systematics
inferredcites →https://doi.org/10.5281/zenodo.16437583openalex-snapshot
A TAXONOMIC COMPARISON OF ARISTIDA TERNIPES AND ARISTIDA HAMULOSA (GRAMINEAE)
inferredcites →https://doi.org/10.5642/aliso.19981702.03openalex-snapshot
Cladistic Parsimony Analysis of Internal Transcribed Spacer Region (nrDNA) Sequences of Bouteloua and Relatives (Gramineae: Chloridoideae)
inferredcites →https://doi.org/10.5642/aliso.20062201.51openalex-snapshot
Phlogeny and Biogeography of the Prayer Plant Family
inferredcites →https://doi.org/10.5642/aliso.20072301.38openalex-snapshot
Phylogenetic Relationships Within the Centothecoideae + Panicoideae Clade (Poaceae) Based on ndhF and rpl16 Intron Sequences and Structural Data
inferredcites →https://doi.org/10.5642/aliso.20072301.42openalex-snapshot
Phylogenetics of Chloridoideae (Gramineae): a Preliminary Study Based on Nuclear Ribosomal Internal Transcribed Spacer and Chloroplast trnL–F Sequences
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.11646/phytotaxa.362.1.9zenodo-depositor-declared
Aristida tovariana (Poaceae, Aristidoideae), a new species from the Andes of Southern Peru
inferred← citeshttps://doi.org/10.11646/phytotaxa.393.1.6zenodo-depositor-declared
Lifeforms as criterion for species delimitation: Are Aristida adscensionis and A. coerulescens (Aristidoideae, Poaceae) two species?
inferred← citeshttps://doi.org/10.11646/phytotaxa.578.1.4zenodo-depositor-declared
Leaf micromorphology and anatomy in the tribe Aristideae (Poaceae) in Iran and its systematic implications
inferred← citeshttps://doi.org/10.1002/ajb2.16286openalex-snapshot
Smut fungus (Langdonia walkerae) incidence is lower in two bunchgrass species (Aristida stricta and A. beyrichiana) after fires early in the year
inferred← citeshttps://doi.org/10.1002/ajb2.70192openalex-snapshot
Evaluating the African arid corridor hypothesis: A meta‐analysis including the phylogenetic and biogeographical history of Sesamothamnus
inferred← citeshttps://doi.org/10.1007/s00442-018-4191-6openalex-snapshot
Some like it hot: the physiological ecology of C4 plant evolution
inferred← citeshttps://doi.org/10.1007/s10539-020-09775-xopenalex-snapshot
The evolutionary community concept is fully armed and operational: a reply to Sagoff
inferred← citeshttps://doi.org/10.1007/s11104-016-2984-0openalex-snapshot
Effects of nitrogen availability on the competitive interactions between an invasive and a native grass from Brazilian cerrado
inferred← citeshttps://doi.org/10.1007/s11557-021-01750-4openalex-snapshot
More than meets the eye — unexpected diversity in downy mildews (Oomycetes) on grasses in Australia
inferred← citeshttps://doi.org/10.1016/j.dib.2026.113043openalex-snapshot
Enhanced DNA barcode datasets for Aristida grasses: new whole genome skimming data for the protected species Aristida triseta Keng integrated with public sequences
inferred← citeshttps://doi.org/10.1016/j.flora.2025.152681openalex-snapshot
Variability of Bilobate silicomorphs in different species of Aristida L. from Western Ghats part of Maharashtra, India and its systematic and environmental implications
inferred← citeshttps://doi.org/10.1016/j.geoderma.2026.117788openalex-snapshot
The influence of tropical grass species on soil nitrification and denitrification across savanna ecosystems
inferred← citeshttps://doi.org/10.1016/j.ympev.2026.108607openalex-snapshot
Geological events and climate oscillations shaped the divergence and evolutionary history of Rehmannia species (Orobanchaceae)
inferred← citeshttps://doi.org/10.1079/cabicompendium.119794openalex-snapshot
Aristida ternipes (spidergrass)
inferred← citeshttps://doi.org/10.1093/aobpla/plag012openalex-snapshot
Severe inbreeding depression in an ecologically important grass is revealed by examining germination, not seed production
inferred← citeshttps://doi.org/10.1093/jxb/eru395openalex-snapshot
From museums to genomics: old herbarium specimens shed light on a C3 to C4 transition
inferred← citeshttps://doi.org/10.1111/1365-2664.70041openalex-snapshot
Fire season and drought influence fire effects on invasive grasses: A meta‐analysis
inferred← citeshttps://doi.org/10.1111/geb.13747openalex-snapshot
Longleaf pine savannas reveal biases in current understanding of savanna biogeography
inferred← citeshttps://doi.org/10.1111/jse.12150openalex-snapshot
A worldwide phylogenetic classification of the Poaceae (Gramineae)
inferred← citeshttps://doi.org/10.1111/jse.12262openalex-snapshot
A worldwide phylogenetic classification of the Poaceae (Gramineae) II: An update and a comparison of two 2015 classifications
inferred← citeshttps://doi.org/10.1111/jse.12857openalex-snapshot
Grasses through space and time: An overview of the biogeographical and macroevolutionary history of Poaceae
inferred← citeshttps://doi.org/10.1111/nph.13033openalex-snapshot
The evolutionary ecology of C 4 plants
inferred← citeshttps://doi.org/10.12664/mycobiota.2015.05.03openalex-snapshot
First record of Langdonia aristidae (Ustilaginales) from Madagascar
inferred← citeshttps://doi.org/10.1371/journal.pone.0097722openalex-snapshot
C4 Photosynthesis Promoted Species Diversification during the Miocene Grassland Expansion
inferred← citeshttps://doi.org/10.14522/darwiniana.2016.41.682openalex-snapshot
ARISTIDA PSEUDOCHICLAYENSIS (POACEAE), UNA ESPECIE NUEVA DEL NORTE DE PERÚ
inferred← citeshttps://doi.org/10.14522/darwiniana.2022.102.1071openalex-snapshot
Aristida diego-santiagoii, una nueva especie de Aristida (Poaceae) para Perú
inferred← citeshttps://doi.org/10.1590/1676-0611-bn-2022-1445openalex-snapshot
Rediscovery of presumably extinct species of Aristida in São Paulo State, Brazil
inferred← citeshttps://doi.org/10.21829/abm126.2019.1379openalex-snapshot
Riqueza de especies, clasificación y listado de las gramíneas (Poaceae) de México
inferred← citeshttps://doi.org/10.3114/fuse.2021.08.04openalex-snapshot
Morphological and molecular characterization of Langdonia walkerae sp. nov. infecting Aristida stricta and A. beyrichiana in longleaf pine-grassland ecosystems in the southeastern USA
inferred← citeshttps://doi.org/10.31610/zsr/2019.28.1.155openalex-snapshot
Leafhoppers of the subtribe Paradorydiina Evans (Hemiptera, Auchenorrhyncha: Cicadellidae) in the United Arab Emirates
inferred← citeshttps://doi.org/10.3390/biology11010063openalex-snapshot
Comparative and Phylogenetic Analysis of Complete Plastomes among Aristidoideae Species (Poaceae)
inferred← citeshttps://doi.org/10.3897/phytokeys.163.38393openalex-snapshot
Checklist of the grasses of India
inferred← citeshttps://doi.org/10.3897/phytokeys.47.8347openalex-snapshot
Plant endemism in the Sierras of Córdoba and San Luis (Argentina): understanding links between phylogeny and regional biogeographical patterns1
inferred← citeshttps://doi.org/10.5958/2231-1750.2015.00017.7openalex-snapshot
Diversity of Aristida L. [Poaceae] and its Extensive Geographical Distribution in India
inferred← citeshttps://doi.org/10.7740/kjcs.2021.66.3.220openalex-snapshot
Evolution and Breeding of Members of Pooideae Subfamily: Focusing on Upland Cereal Crops
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