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Assembling the Tree of the Monocotyledons: Plastome Sequence Phylogeny and Evolution of Poales 1
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/j.1537-2197.1989.tb15145.xopenalex-snapshot
WIND POLLINATION, SELF‐INCOMPATIBILITY, AND ALTITUDINAL SHIFTS IN POLLINATION SYSTEMS IN THE HIGH ANDEAN GENUS ESPELETIA (ASTERACEAE)
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/10.1002/tax.574004openalex-snapshot
Phylogeny and evolutionary patterns in Nymphaeales: integrating genes, genomes and morphology
inferredcites →https://doi.org/10.1006/anbo.1994.1145openalex-snapshot
Investigation of the Presence of Phenolic Compounds in Monocotyledonous Cell Walls, using UV Fluorescence Microscopy
inferredcites →https://doi.org/10.1006/bojl.2000.0380openalex-snapshot
Angiosperm phylogeny inferred from 18S rDNA, rbcL, and atpB sequences
inferredcites →https://doi.org/10.1006/jmbi.1995.0460openalex-snapshot
Complete Sequence of the Maize Chloroplast Genome: Gene Content, Hotspots of Divergence and Fine Tuning of Genetic Information by Transcript Editing
inferredcites →https://doi.org/10.1006/mpev.1997.0409openalex-snapshot
Consistency, Characters, and the Likelihood of Correct Phylogenetic Inference
inferredcites →https://doi.org/10.1006/mpev.1999.0601openalex-snapshot
Polyphyly and Convergent Morphological Evolution in Commelinales and Commelinidae: Evidence from rbcL Sequence Data
inferredcites →https://doi.org/10.1007/978-1-4615-1773-3_24openalex-snapshot
Species, Nitrogen, and Grassland Dynamics: The Constraints of Stuff
inferredcites →https://doi.org/10.1007/978-3-642-61663-1openalex-snapshot
The Families of the Monocotyledons
inferredcites →https://doi.org/10.1007/bf00055101openalex-snapshot
Insect-induced wind pollination of the palm Chamaedorea pinnatifrons and pollination in the related Wendlandiella sp.
inferredcites →https://doi.org/10.1007/bf00160154openalex-snapshot
Maximum likelihood phylogenetic estimation from DNA sequences with variable rates over sites: Approximate methods
inferredcites →https://doi.org/10.1007/bf00161167openalex-snapshot
Relative rates of nucleotide substitution at the rbcl locus of monocotyledonous plants
inferredcites →https://doi.org/10.1007/bf00323782openalex-snapshot
Controls of nitrogen limitation in tallgrass prairie
inferredcites →https://doi.org/10.1007/bf00936149openalex-snapshot
Floral biological observations onHeliamphora tatei (Sarraceniaceae) and other plants from Cerro de la Neblina in Venezuela
inferredcites →https://doi.org/10.1007/bf00985442openalex-snapshot
Phylogenetics of the slipper orchids (Cypripedioideae, Orchidaceae): Nuclear rDNA ITS sequences
inferredcites →https://doi.org/10.1007/bf02464880openalex-snapshot
The complete sequence of the rice (Oryza sativa) chloroplast genome: Intermolecular recombination between distinct tRNA genes accounts for a major plastid DNA inversion during the evolution of the cereals
inferredcites →https://doi.org/10.1007/bf02860996openalex-snapshot
A review of pollination studies in the Palmae
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/bf02935930openalex-snapshot
The Nucellus and Chalaza in monocotyledons: Structure and systematics
inferredcites →https://doi.org/10.1007/s00122-007-0567-4openalex-snapshot
Complete chloroplast genome sequences of Hordeum vulgare, Sorghum bicolor and Agrostis stolonifera, and comparative analyses with other grass genomes
inferredcites →https://doi.org/10.1007/s00239-008-9091-7openalex-snapshot
Complete Sequence of the Duckweed (Lemna minor) Chloroplast Genome: Structural Organization and Phylogenetic Relationships to Other Angiosperms
inferredcites →https://doi.org/10.1007/s00239-009-9275-9openalex-snapshot
The Complete Chloroplast Genome of Coix lacryma-jobi and a Comparative Molecular Evolutionary Analysis of Plastomes in Cereals
inferredcites →https://doi.org/10.1007/s00239-009-9317-3openalex-snapshot
Implications of the Plastid Genome Sequence of Typha (Typhaceae, Poales) for Understanding Genome Evolution in Poaceae
inferredcites →https://doi.org/10.1007/s00438-001-0606-9openalex-snapshot
Structural features of a wheat plastome as revealed by complete sequencing of chloroplast DNA
inferredcites →https://doi.org/10.1007/s00606-003-0056-4openalex-snapshot
The chloroplast genome of the ?basal? angiosperm Calycanthus fertilis ? structural and phylogenetic analyses
inferredcites →https://doi.org/10.1007/s00606-008-0135-7openalex-snapshot
DNA variation within Juncaceae: comparison of impact of organelle regions on phylogeny
inferredcites →https://doi.org/10.1007/s11101-009-9146-4openalex-snapshot
The distribution of ester-linked ferulic acid in the cell walls of angiosperms
inferredcites →https://doi.org/10.1007/s11104-006-9002-xopenalex-snapshot
Competition for Nutrients and Optimal Root Allocation
inferredcites →https://doi.org/10.1007/s11248-006-9009-3openalex-snapshot
Transformation of poplar (Populus alba) plastids and expression of foreign proteins in tree chloroplasts
inferredcites →https://doi.org/10.1007/s12229-008-9019-3openalex-snapshot
Phylogeny of Cyperaceae Based on DNA Sequence Data: Current Progress and Future Prospects
inferredcites →https://doi.org/10.1016/0025-5564(95)00172-7openalex-snapshot
Inconsistency of evolutionary tree topology reconstruction methods when substitution rates vary across characters
inferredcites →https://doi.org/10.1016/0305-1978(80)90008-3openalex-snapshot
Phenolic constituents of the cell walls of monocotyledons
inferredcites →https://doi.org/10.1016/b978-0-12-583980-8.50012-0openalex-snapshot
Wind Pollination: Some Ecological and Evolutionary Perspectives
inferredcites →https://doi.org/10.1016/c2009-0-00736-3openalex-snapshot
Principles of Pollination Ecology
inferredcites →https://doi.org/10.1016/j.bse.2004.12.004openalex-snapshot
Floral scent of Eleocharis elegans (Kunth) Roem. & Schult. (Cyperaceae)
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.tree.2007.01.012openalex-snapshot
Deciphering ancient rapid radiations
inferredcites →https://doi.org/10.1016/j.ympev.2003.10.010openalex-snapshot
Utility of plastid psaB gene sequences for investigating intrafamilial relationships within Orchidaceae
inferredcites →https://doi.org/10.1016/j.ympev.2007.06.004openalex-snapshot
Phylogenetic and evolutionary implications of complete chloroplast genome sequences of four early-diverging angiosperms: Buxus (Buxaceae), Chloranthus (Chloranthaceae), Dioscorea (Dioscoreaceae), and Illicium (Schisandraceae)
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.2010.03.003openalex-snapshot
Phylogenetic relationships within Orchidaceae based on a low-copy nuclear coding gene, Xdh: Congruence with organellar and nuclear ribosomal DNA results
inferredcites →https://doi.org/10.1016/s0074-7696(08)61084-0openalex-snapshot
Wind Pollination Mechanisms and Aerobiology
inferredcites →https://doi.org/10.1016/s0076-6879(05)95020-9openalex-snapshot
Methods for Obtaining and Analyzing Whole Chloroplast Genome Sequences
inferredcites →https://doi.org/10.1016/s0169-5347(02)02540-5openalex-snapshot
The evolution of wind pollination in angiosperms
inferredcites →https://doi.org/10.1023/a:1006478403810openalex-snapshot
The plastid chromosome of spinach (Spinacia oleracea): complete nucleotide sequence and gene organization
inferredcites →https://doi.org/10.1038/nature05612openalex-snapshot
Hydatellaceae identified as a new branch near the base of the angiosperm phylogenetic tree
inferredcites →https://doi.org/10.1038/nature06039openalex-snapshot
Dating the origin of the Orchidaceae from a fossil orchid with its pollinator
inferredcites →https://doi.org/10.1046/j.1095-8339.2003.t01-1-00158.xopenalex-snapshot
An update of the Angiosperm Phylogeny Group classification for the orders and families of flowering plants: APG II
inferredcites →https://doi.org/10.1055/s-2000-5953openalex-snapshot
A Phylogenetic Analysis of the Plastid matK Gene with Emphasis on Melanthiaceae sensu lato
inferredcites →https://doi.org/10.1055/s-2004-821278openalex-snapshot
Biosystematic Studies on the Family Tofieldiaceae I. Phylogeny and Circumscription of the Family Inferred from DNA Sequences of matK and rbcL
inferredcites →https://doi.org/10.1071/bt08119openalex-snapshot
Pollination biology of Syngonanthus elegans (Eriocaulaceae – Poales)
inferredcites →https://doi.org/10.1071/sb08050openalex-snapshot
Early Eocene Ripogonum (Liliales: Ripogonaceae) leaf macrofossils from southern Australia
inferredcites →https://doi.org/10.1073/pnas.0407174101openalex-snapshot
Araceae from the Early Cretaceous of Portugal: Evidence on the emergence of monocotyledons
inferredcites →https://doi.org/10.1073/pnas.0708072104openalex-snapshot
Using plastid genome-scale data to resolve enigmatic relationships among basal angiosperms
inferredcites →https://doi.org/10.1073/pnas.0709121104openalex-snapshot
Analysis of 81 genes from 64 plastid genomes resolves relationships in angiosperms and identifies genome-scale evolutionary patterns
inferredcites →https://doi.org/10.1073/pnas.080421597openalex-snapshot
Early Cretaceous lineages of monocot flowering plants
inferredcites →https://doi.org/10.1073/pnas.0813376106openalex-snapshot
Rosid radiation and the rapid rise of angiosperm-dominated forests
inferredcites →https://doi.org/10.1073/pnas.0909672107openalex-snapshot
Phylogenetic analyses reveal the shady history of C 4 grasses
inferredcites →https://doi.org/10.1073/pnas.89.16.7722openalex-snapshot
Chloroplast DNA inversions and the origin of the grass family (Poaceae).
inferredcites →https://doi.org/10.1073/pnas.90.10.4641openalex-snapshot
Phylogenetic analysis of rbcL sequences identifies Acorus calamus as the primal extant monocotyledon.
inferredcites →https://doi.org/10.1073/pnas.93.19.10274openalex-snapshot
Substitution rate comparisons between grasses and palms: synonymous rate differences at the nuclear gene Adh parallel rate differences at the plastid gene rbcL.
inferredcites →https://doi.org/10.1078/0367-2530-00090openalex-snapshot
Floral anatomy of Eriocaulon elichrysoides and Syngonanthus caulescens (Eriocaulaceae)
inferredcites →https://doi.org/10.1080/00173139309429987openalex-snapshot
Exine Sculpture inParianaPollen (Gramineae)
inferredcites →https://doi.org/10.1080/0028825x.1976.10428894openalex-snapshot
Hydatellaceae — a new family of monocotyledoneae
inferredcites →https://doi.org/10.1080/0028825x.1986.10409725openalex-snapshot
The avoidance of interference between the presentation of pollen and stigmas in angiosperms I. Dichogamy
inferredcites →https://doi.org/10.1080/0028825x.1986.10409726openalex-snapshot
The avoidance of interference between the presentation of pollen and stigmas in angiosperms II. Herkogamy
inferredcites →https://doi.org/10.1080/10635150117959openalex-snapshot
Bias in Phylogenetic Estimation and Its Relevance to the Choice between Parsimony and Likelihood Methods
inferredcites →https://doi.org/10.1080/106351501753462885openalex-snapshot
Unraveling the Evolutionary Radiation of the Families of the Zingiberales Using Morphological and Molecular Evidence
inferredcites →https://doi.org/10.1080/106351502753475899openalex-snapshot
A Molecular Phylogenetic Study of the Palmae (Arecaceae) Based on atpB, rbcL, and 18S nrDNA Sequences
inferredcites →https://doi.org/10.1080/10635150390132911openalex-snapshot
Is Sparse Taxon Sampling a Problem for Phylogenetic Inference?
inferredcites →https://doi.org/10.1080/10635150701499563openalex-snapshot
Experimental Design Criteria in Phylogenetics: Where to Add Taxa
inferredcites →https://doi.org/10.1080/106351598260996openalex-snapshot
Is It Better to Add Taxa or Characters to a Difficult Phylogenetic Problem?
inferredcites →https://doi.org/10.1080/106351598261012openalex-snapshot
Inferring Complex Phylogenies Using Parsimony: An Empirical Approach Using Three Large DNA Data Sets for Angiosperms
inferredcites →https://doi.org/10.1086/284014openalex-snapshot
Selection of Combined Versus Separate Sexes in Seed Plants
inferredcites →https://doi.org/10.1086/284325openalex-snapshot
Phylogenies and the Comparative Method
inferredcites →https://doi.org/10.1086/285485openalex-snapshot
Why are Unisexual Flowers Associated with Wind Pollination and Unspecialized Pollinators?
inferredcites →https://doi.org/10.1086/421067openalex-snapshot
Ancient Vicariance or Recent Long‐Distance Dispersal? Inferences about Phylogeny and South American–African Disjunctions in Rapateaceae and Bromeliaceae Based onndhF Sequence Data
inferredcites →https://doi.org/10.1086/431800openalex-snapshot
Phylogenetic Analyses of Basal Angiosperms Based on Nine Plastid, Mitochondrial, and Nuclear Genes
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/10.1086/519857openalex-snapshot
Resource Use Patterns Predict Long‐Term Outcomes of Plant Competition for Nutrients and Light
inferredcites →https://doi.org/10.1086/523365openalex-snapshot
A Phylogenetic Analysis of the Evolution of Wind Pollination in the Angiosperms
inferredcites →https://doi.org/10.1093/aob/mci191openalex-snapshot
Pollination in Brazilian Syngonanthus (Eriocaulaceae) Species: Evidence for Entomophily Instead of Anemophily
inferredcites →https://doi.org/10.1093/aob/mcl231openalex-snapshot
Floral Anatomy of Paepalanthoideae (Eriocaulaceae, Poales) and their Nectariferous Structures
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/aob/mcr213openalex-snapshot
Diversity, phylogeny, and evolution in the monocotyledons
inferredcites →https://doi.org/10.1093/bioinformatics/bth352openalex-snapshot
Automatic annotation of organellar genomes with DOGMA
inferredcites →https://doi.org/10.1093/bioinformatics/btl446openalex-snapshot
RAxML-VI-HPC: maximum likelihood-based phylogenetic analyses with thousands of taxa and mixed models
inferredcites →https://doi.org/10.1093/dnares/11.2.93openalex-snapshot
Complete Nucleotide Sequence of the Sugarcane (Saccharum Officinarum) Chloroplast Genome: A Comparative Analysis of Four Monocot Chloroplast Genomes
inferredcites →https://doi.org/10.1093/dnares/11.4.247openalex-snapshot
Complete Chloroplast Genome Sequences from Korean Ginseng (Panax schinseng Nees) and Comparative Analysis of Sequence Evolution among 17 Vascular Plants
inferredcites →https://doi.org/10.1093/molbev/msg159openalex-snapshot
Analysis of the Amborella trichopoda Chloroplast Genome Sequence Suggests That Amborella Is Not a Basal Angiosperm
inferredcites →https://doi.org/10.1093/molbev/msh147openalex-snapshot
The Chloroplast Genome of Nymphaea alba: Whole-Genome Analyses and the Problem of Identifying the Most Basal Angiosperm
inferredcites →https://doi.org/10.1093/molbev/msi173openalex-snapshot
Analysis of Acorus calamus Chloroplast Genome and Its Phylogenetic Implications
inferredcites →https://doi.org/10.1093/molbev/msi212openalex-snapshot
Maximum Likelihood Outperforms Maximum Parsimony Even When Evolutionary Rates Are Heterotachous
inferredcites →https://doi.org/10.1093/molbev/msj029openalex-snapshot
The Chloroplast Genome of Phalaenopsis aphrodite (Orchidaceae): Comparative Analysis of Evolutionary Rate with that of Grasses and Its Phylogenetic Implications
inferredcites →https://doi.org/10.1093/nar/gkh340openalex-snapshot
MUSCLE: multiple sequence alignment with high accuracy and high throughput
inferredcites →https://doi.org/10.1093/oxfordjournals.aob.a085414openalex-snapshot
The Receptive Surface of the Angiosperm Stigma
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040261openalex-snapshot
The robustness of two phylogenetic methods: four-taxon simulations reveal a slight superiority of maximum likelihood over neighbor joining.
inferredcites →https://doi.org/10.1093/pcp/pcm170openalex-snapshot
The Model Plant Medicago truncatula Exhibits Biparental Plastid Inheritance
inferredcites →https://doi.org/10.1093/sysbio/40.3.315openalex-snapshot
The Discovery and Importance of Multiple Islands of Most-Parsimonious Trees
inferredcites →https://doi.org/10.1093/sysbio/42.3.247openalex-snapshot
Success of Phylogenetic Methods in the Four-Taxon Case
inferredcites →https://doi.org/10.1093/sysbio/syp021openalex-snapshot
Complete Generic-Level Phylogenetic Analyses of Palms (Arecaceae) with Comparisons of Supertree and Supermatrix Approaches
inferredcites →https://doi.org/10.1093/treephys/tpp015openalex-snapshot
Complete nucleotide sequence of Dendrocalamus latiflorus and Bambusa oldhamii chloroplast genomes
inferredcites →https://doi.org/10.1098/rspb.2001.1782openalex-snapshot
Evolution of the angiosperms: calibrating the family tree
inferredcites →https://doi.org/10.1098/rspb.2004.2849openalex-snapshot
Environmental energy and evolutionary rates in flowering plants
inferredcites →https://doi.org/10.1098/rspb.2005.3067openalex-snapshot
Repeated evolution of net venation and fleshy fruits among monocots in shaded habitats confirms a priori predictions: evidence from an ndhF phylogeny
inferredcites →https://doi.org/10.1098/rstb.1991.0070openalex-snapshot
Abiotic pollination: an evolutionary escape for animal-pollinated angiosperms
inferredcites →https://doi.org/10.1101/gr.1917404openalex-snapshot
Using the miraEST Assembler for Reliable and Automated mRNA Transcript Assembly and SNP Detection in Sequenced ESTs
inferredcites →https://doi.org/10.1101/gr.8.3.195openalex-snapshot
Consed: A Graphical Tool for Sequence Finishing
inferredcites →https://doi.org/10.1111/boj.12385openalex-snapshot
An update of the Angiosperm Phylogeny Group classification for the orders and families of flowering plants: APG IV
inferredcites →https://doi.org/10.1111/j.0014-3820.2000.tb01237.xopenalex-snapshot
MOLECULAR EVOLUTION, ADAPTIVE RADIATION, AND GEOGRAPHIC DIVERSIFICATION IN THE AMPHIATLANTIC FAMILY RAPATEACEAE: EVIDENCE FROM ndhF SEQUENCES AND MORPHOLOGY
inferredcites →https://doi.org/10.1111/j.0014-3820.2002.tb01451.xopenalex-snapshot
GONDWANAN EVOLUTION OF THE GRASS ALLIANCE OF FAMILIES (POALES)
inferredcites →https://doi.org/10.1111/j.0014-3820.2003.tb01513.xopenalex-snapshot
CONTRASTING PATTERNS OF RADIATION IN AFRICAN AND AUSTRALIAN RESTIONACEAE
inferredcites →https://doi.org/10.1111/j.0030-1299.2004.12687.xopenalex-snapshot
Bottom‐up control and co‐occurrence in complex communities: honeydew and nectar determine a rainforest ant mosaic
inferredcites →https://doi.org/10.1111/j.1095-8339.1988.tb01584.xopenalex-snapshot
Development of ovule and seed in Rapateaceae
inferredcites →https://doi.org/10.1111/j.1095-8339.2004.00345.xopenalex-snapshot
The age of major monocot groups inferred from 800+rbcL sequences
inferredcites →https://doi.org/10.1111/j.1095-8339.2009.00996.xopenalex-snapshot
An update of the Angiosperm Phylogeny Group classification for the orders and families of flowering plants: APG III
inferredcites →https://doi.org/10.1111/j.1365-2656.2004.00789.xopenalex-snapshot
Preferences for sugars and amino acids and their conditionality in a diverse nectar‐feeding ant community
inferredcites →https://doi.org/10.1111/j.1442-9993.2004.01380.xopenalex-snapshot
Sugar and amino acid composition of ant‐attended nectar and honeydew sources from an Australian rainforest
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.1558-5646.1977.tb00979.xopenalex-snapshot
POLLEN-OVULE RATIOS: A CONSERVATIVE INDICATOR OF BREEDING SYSTEMS IN FLOWERING PLANTS
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/10.1126/science.1163197openalex-snapshot
Rates of Molecular Evolution Are Linked to Life History in Flowering Plants
inferredcites →https://doi.org/10.1127/0340-269x/2005/0035-0201openalex-snapshot
Ephemeral wetland vegetation of Western Australia
inferredcites →https://doi.org/10.1139/b08-063openalex-snapshot
Phylogenetic relationships in the monocot order Commelinales, with a focus on PhilydraceaeThis paper is one of a selection of papers published in the Special Issue on Systematics Research.
inferredcites →https://doi.org/10.1139/b09-093openalex-snapshot
Inference of phylogenetic relationships among the subfamilies of grasses (Poaceae: Poales) using meso-scale exemplar-based sampling of the plastid genome
inferredcites →https://doi.org/10.1146/annurev.ecolsys.31.1.217openalex-snapshot
The Grasses: A Case Study in Macroevolution
inferredcites →https://doi.org/10.1146/annurev.ecolsys.36.102403.135635openalex-snapshot
Evolutionary History of Poales
inferredcites →https://doi.org/10.1146/annurev.ento.44.1.183openalex-snapshot
THE ROLE OF STINGLESS BEES IN CROP POLLINATION
inferredcites →https://doi.org/10.1146/annurev.es.07.110176.002023openalex-snapshot
Why Bamboos Wait So Long to Flower
inferredcites →https://doi.org/10.1146/annurev.es.13.110182.002433openalex-snapshot
Pollination by Wind and Animals: Ecology of Geographic Patterns
inferredcites →https://doi.org/10.1186/1471-2148-6-32openalex-snapshot
Phylogenetic analyses of Vitis (Vitaceae) based on complete chloroplast genome sequences: effects of taxon sampling and phylogenetic methods on resolving relationships among rosids
inferredcites →https://doi.org/10.1186/1471-2148-6-77openalex-snapshot
Complete plastid genome sequences of Drimys, Liriodendron, and Piper: implications for the phylogenetic relationships of magnoliids
inferredcites →https://doi.org/10.1186/1471-2148-7-s1-s4openalex-snapshot
Suppression of long-branch attraction artefacts in the animal phylogeny using a site-heterogeneous model
inferredcites →https://doi.org/10.1186/1471-2164-8-174openalex-snapshot
Comparative chloroplast genomics: analyses including new sequences from the angiosperms Nuphar advena and Ranunculus macranthus
inferredcites →https://doi.org/10.1186/1471-2229-6-17openalex-snapshot
Rapid and accurate pyrosequencing of angiosperm plastid genomes.
inferredcites →https://doi.org/10.1590/s0100-204x2008000300001openalex-snapshot
Polinização do dendezeiro por besouros no sul da Bahia
inferredcites →https://doi.org/10.1600/0363644041744365openalex-snapshot
A Phylogeny of the Monocots, as Inferred from rbcL and atpA Sequence Variation, and a Comparison of Methods for Calculating Jackknife and Bootstrap Values
inferredcites →https://doi.org/10.1600/0363644053661931openalex-snapshot
Phylogeny of Orchidantha (Lowiaceae) and the Zingiberales Based on Six DNA Regions
inferredcites →https://doi.org/10.1600/036364407780360102openalex-snapshot
Reinstatement and Emendation of Subfamily Micrairoideae (Poaceae)
inferredcites →https://doi.org/10.1663/0007-196x(2003)055[0214:rotmfp]2.0.co;2openalex-snapshot
Recircumscription of the monocotyledonous family Petrosaviaceae to include Japonolirion
inferredcites →https://doi.org/10.1890/0012-9658(1997)078[2359:fnaapr]2.0.co;2openalex-snapshot
FIRE, N AVAILABILITY, AND PLANT RESPONSE IN GRASSLANDS: A TEST OF THE TRANSIENT MAXIMA HYPOTHESIS
inferredcites →https://doi.org/10.1890/04-0407openalex-snapshot
ECOLOGICAL CONSEQUENCES OF C4GRASS INVASION OF A C4GRASSLAND: A DILEMMA FOR MANAGEMENT
inferredcites →https://doi.org/10.1890/08-0116.1openalex-snapshot
A fungus among us: broad patterns of endophyte distribution in the grasses
inferredcites →https://doi.org/10.2193/2007-045openalex-snapshot
African Grazing Lawns—How Fire, Rainfall, and Grazer Numbers Interact to Affect Grass Community States
inferredcites →https://doi.org/10.2307/2388036openalex-snapshot
A Commentary on the Bamboos (Poaceae: Bambusoideae)
inferredcites →https://doi.org/10.2307/2398809openalex-snapshot
Some Evolutionary Trends in the Bambusoideae (Poaceae)
inferredcites →https://doi.org/10.2307/2398810openalex-snapshot
Evolution of Reproductive Systems in the Gramineae
inferredcites →https://doi.org/10.2307/2399846openalex-snapshot
Phylogenetics of Seed Plants: An Analysis of Nucleotide Sequences from the Plastid Gene rbcL
inferredcites →https://doi.org/10.2307/2399849openalex-snapshot
Phylogenetic Hypotheses for the Monocotyledons Constructed from rbcL Sequence Data
inferredcites →https://doi.org/10.2307/2407542openalex-snapshot
Pollen-Ovule Ratios: A Conservative Indicator of Breeding Systems in Flowering Plants
inferredcites →https://doi.org/10.2307/2419593openalex-snapshot
Molecular Evolution and Adaptive Radiation.
inferredcites →https://doi.org/10.2307/2419803openalex-snapshot
A Phylogeny of the Grass Family (Poaceae) Based on ndhF Sequence Data
inferredcites →https://doi.org/10.2307/2419820openalex-snapshot
Phylogenetic Studies in Alismatidae, II: Evolution of Marine Angiosperms (Seagrasses) and Hydrophily
inferredcites →https://doi.org/10.2307/2445418openalex-snapshot
Dioecy and Its Correlates in the Flowering Plants
inferredcites →https://doi.org/10.2307/2446396openalex-snapshot
Dioecy and the evolution of pollination systems in Schiedea and Alsinidendron (Caryophyllaceae: Alsinoideae) in the Hawaiian Islands
inferredcites →https://doi.org/10.2307/2656611openalex-snapshot
Wind pollination and reproductive assurance in Linanthus parviflorus (Polemoniaceae), a self‐incompatible annual
inferredcites →https://doi.org/10.2307/2666637openalex-snapshot
The Puelioideae, A New Subfamily of Poaceae
inferredcites →https://doi.org/10.2307/2806385openalex-snapshot
The Monocotyledons. A Comparative Study
inferredcites →https://doi.org/10.2307/2989701openalex-snapshot
Insect Pollination in Tropical Rain Forest Grasses
inferredcites →https://doi.org/10.2307/2992015openalex-snapshot
An Ordinal Classification for the Families of Flowering Plants
inferredcites →https://doi.org/10.2307/2992325openalex-snapshot
The Discovery and Importance of Multiple Islands of Most-Parsimonious Trees
inferredcites →https://doi.org/10.2307/2997255openalex-snapshot
Advances in Angiosperm Systematics: Examples from the Liliales and Asparagales
inferredcites →https://doi.org/10.2307/3235637openalex-snapshot
Centrolepidi‐Hydrocotyletea alatae, a new class of ephemeral communities in Western Australia*
inferredcites →https://doi.org/10.2307/3298585openalex-snapshot
Phylogeny and Subfamilial Classification of the Grasses (Poaceae)
inferredcites →https://doi.org/10.2307/4109686openalex-snapshot
The Evolutionary History of the Poales/Restionales: A Hypothesis
inferredcites →https://doi.org/10.2307/4117102openalex-snapshot
A Scanning Electron Microscope Survey of Grass Pollen
inferredcites →https://doi.org/10.2478/s11658-007-0029-7openalex-snapshot
The complete structure of the cucumber (Cucumis sativus L.) chloroplast genome: Its composition and comparative analysis
inferredcites →https://doi.org/10.3732/ajb.0900033openalex-snapshot
Seed fertilization, development, and germination in Hydatellaceae (Nymphaeales): Implications for endosperm evolution in early angiosperms
inferredcites →https://doi.org/10.3732/ajb.0900074openalex-snapshot
Morphology and development of the gynoecium in Centrolepidaceae: The most remarkable range of variation in Poales
inferredcites →https://doi.org/10.3732/ajb.0900226openalex-snapshot
The chloroplast genome of Anomochloa marantoidea (Anomochlooideae; Poaceae) comprises a mixture of grass‐like and unique features
inferredcites →https://doi.org/10.3732/ajb.90.1.93openalex-snapshot
Phylogenetic relationships among Poaceae and related families as inferred from morphology, inversions in the plastid genome, and sequence data from the mitochondrial and plastid genomes
inferredcites →https://doi.org/10.3732/ajb.90.7.1071openalex-snapshot
Phylogenetic relationships in Cyperaceae subfamily Mapanioideae inferred from pollen and plastid DNA sequence data
inferredcites →https://doi.org/10.3732/ajb.91.10.1645openalex-snapshot
Monocot relationships: an overview
inferredcites →https://doi.org/10.3732/ajb.91.6.997openalex-snapshot
Amborella not a “basal angiosperm”? Not so fast
inferredcites →https://doi.org/10.3732/ajb.91.9.1364openalex-snapshot
Testing the adaptive nature of radiation: growth form and life history divergence in the African grass genus Ehrharta (Poaceae: Ehrhartoideae)
inferredcites →https://doi.org/10.5642/aliso.20062201.02openalex-snapshot
Robust Inference of Monocot Deep Phylogeny Using an Expanded Multigene Plastid Data Set
inferredcites →https://doi.org/10.5642/aliso.20062201.24openalex-snapshot
Phylogeny, Genome Size, and Chromosome Evolution of Asparagales
inferredcites →https://doi.org/10.5642/aliso.20072301.04openalex-snapshot
Phylogeny, Adaptive Radiation, and Historical Biogeography of Bromeliaceae Inferred from ndhF Sequence Data
inferredcites →https://doi.org/10.5642/aliso.20072301.19openalex-snapshot
Large Trees, Supertrees, and Diversification of the Grass Family
inferredcites →https://doi.org/10.5860/choice.39-2183openalex-snapshot
MacClade 4.0: analysis of phylogeny and character evolution
inferredcites →https://doi.org/10.5962/p.185770openalex-snapshot
A Study of the Genus Joinvillea (Flagellariaceae)
inferredcites →https://doi.org/10.7751/telopea19982001openalex-snapshot
Georgeantha hexandra, a new genus and species of Ecdeiocoleaceae (Poales) from Western Australia
inferredcites →https://doi.org/10.7751/telopea20075743openalex-snapshot
Ecdeiocoleaceae and Joinvilleaceae, sisters of Poaceae (Poales): evidence from rbcL and matK data
inferredcites →https://doi.org/10.7751/telopea20095822openalex-snapshot
A new subfamilial and tribal classification of Restionaceae (Poales)
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.574.1.1zenodo-depositor-declared
A checklist of Iranian Grasses
inferred← citeshttps://doi.org/10.1002/9781119312994.apr0622openalex-snapshot
Evolution and Taxonomy of the Grasses (Poaceae): A Model Family for the Study of Species‐Rich Groups
inferred← citeshttps://doi.org/10.1002/ajb2.1016openalex-snapshot
Quartet Sampling distinguishes lack of support from conflicting support in the green plant tree of life
inferred← citeshttps://doi.org/10.1002/ajb2.1048openalex-snapshot
Plastid phylogenomic analysis of green plants: A billion years of evolutionary history
inferred← citeshttps://doi.org/10.1002/ajb2.1070openalex-snapshot
Phylogenomic inference in extremis: A case study with mycoheterotroph plastomes
inferred← citeshttps://doi.org/10.1002/ajb2.1178openalex-snapshot
Monocot plastid phylogenomics, timeline, net rates of species diversification, the power of multi‐gene analyses, and a functional model for the origin of monocots
inferred← citeshttps://doi.org/10.1002/ajb2.1688openalex-snapshot
Phylogenomics and biogeography of Cunoniaceae (Oxalidales) with complete generic sampling and taxonomic realignments
inferred← citeshttps://doi.org/10.1002/ajb2.70153openalex-snapshot
Phylogenomics, ecomorphological evolution, and historical biogeography in Deuterocohnia (Bromeliaceae: Pitcairnioideae)
inferred← citeshttps://doi.org/10.1002/ajb2.70267openalex-snapshot
Placing very long branch taxa in the plant tree of life: A case study with Dioscoreales mycoheterotrophs
inferred← citeshttps://doi.org/10.1002/ajp.23609openalex-snapshot
Dietary flexibility of the greater bamboo lemur ( Prolemur simus ), a specialized feeder, in eastern Madagascar
inferred← citeshttps://doi.org/10.1002/ece3.10630openalex-snapshot
Is there silicon in flowers and what does it tell us?
inferred← citeshttps://doi.org/10.1002/ecy.3636openalex-snapshot
Anthers in blue: A hidden rhapsody in A mazonian E riocaulaceae
inferred← citeshttps://doi.org/10.1007/s00239-019-09920-5openalex-snapshot
In-Silico Evaluation of a New Gene From Wheat Reveals the Divergent Evolution of the CAP160 Homologous Genes Into Monocots
inferred← citeshttps://doi.org/10.1007/s00425-016-2527-1openalex-snapshot
Structural diversity of xylans in the cell walls of monocots
inferred← citeshttps://doi.org/10.1007/s00606-012-0721-6openalex-snapshot
The taxonomic value of floral characters in Rapateaceae (Poales-Monocotyledons)
inferred← citeshttps://doi.org/10.1007/s00606-013-0964-xopenalex-snapshot
Ovule ontogeny in Billbergia nutans in the evolutionary context of Bromeliaceae (Poales)
inferred← citeshttps://doi.org/10.1007/s00606-013-0971-yopenalex-snapshot
Phylogenomics, molecular evolution, and estimated ages of lineages from the deep phylogeny of Poaceae
inferred← citeshttps://doi.org/10.1007/s00606-014-0984-1openalex-snapshot
Leaf and inflorescence peduncle anatomy: a contribution to the taxonomy of Rapateaceae
inferred← citeshttps://doi.org/10.1007/s00606-016-1361-zopenalex-snapshot
Floral anatomy and development of Saxofridericia aculeata (Rapateaceae) and its taxonomic and phylogenetic significance
inferred← citeshttps://doi.org/10.1007/s00606-017-1438-3openalex-snapshot
Floral ontogeny and vasculature in Xyridaceae, with particular reference to staminodes and stylar appendages
inferred← citeshttps://doi.org/10.1007/s00606-019-01592-4openalex-snapshot
Floral organogenesis and vasculature in Mayacaceae, an enigmatic family of Poales
inferred← citeshttps://doi.org/10.1007/s00606-020-01681-9openalex-snapshot
Comparative floral morphology and anatomy of Thurniaceae, an early-diverging family in the cyperids (Poales, Monocotyledons)
inferred← citeshttps://doi.org/10.1007/s00606-022-01825-zopenalex-snapshot
Ecological and evolutionary aspects of seed coat and seedling development in Juncus tenuis (Juncaceae, Poales)
inferred← citeshttps://doi.org/10.1007/s00606-024-01933-yopenalex-snapshot
Genome size variation and whole-genome duplications in the monocot order Poales
inferred← citeshttps://doi.org/10.1007/s00709-020-01583-0openalex-snapshot
Development of the permanent tetrad wall in Juncus L. (Juncaceae, Poales)
inferred← citeshttps://doi.org/10.1007/s11104-015-2764-2openalex-snapshot
Biodiversity hotspots and Ocbil theory
inferred← citeshttps://doi.org/10.1007/s11105-012-0461-3openalex-snapshot
Loss of the Acetyl-CoA Carboxylase (accD) Gene in Poales
inferred← citeshttps://doi.org/10.1007/s11105-013-0616-xopenalex-snapshot
Complete Chloroplast Genome of Chionographis japonica (Willd.) Maxim. (Melanthiaceae): Comparative Genomics and Evaluation of Universal Primers for Liliales
inferred← citeshttps://doi.org/10.1007/s11105-015-0914-6openalex-snapshot
Phylogenetic Inferences and the Evolution of Plastid DNA in Campynemataceae and the Mycoheterotrophic Corsia dispar D.L Jones & B. Gray (Corsiaceae)
inferred← citeshttps://doi.org/10.1007/s12229-012-9096-1openalex-snapshot
Monocot Xylem Revisited: New Information, New Paradigms
inferred← citeshttps://doi.org/10.1007/s12229-012-9103-6openalex-snapshot
Systematic Placement of Dasypogonaceae Among Commelinid Monocots: Evidence from Flowers and Fruits
inferred← citeshttps://doi.org/10.1007/s12229-014-9133-3openalex-snapshot
Epidermal Patterning and Silica Phytoliths in Grasses: An Evolutionary History
inferred← citeshttps://doi.org/10.1007/s12229-018-9202-0openalex-snapshot
Phylogeny and Systematics of Cyperaceae, the Evolution and Importance of Embryo Morphology
inferred← citeshttps://doi.org/10.1007/s13127-018-0384-4openalex-snapshot
The origin and diversification of the Entorrhizales: deep evolutionary roots but recent speciation with a phylogenetic and phenotypic split between associates of the Cyperaceae and Juncaceae
inferred← citeshttps://doi.org/10.1007/s40415-025-01069-4openalex-snapshot
Ambophily ensures high reproductive success in a generalist species: Paepalanthus calvus (Eriocaulaceae) as study case
inferred← citeshttps://doi.org/10.1016/b978-0-12-812628-8.50007-9openalex-snapshot
Diversity and Classification of Flowering Plants: Amborellales, Nymphaeales, Austrobaileyales, Magnoliids, Monocots, and Ceratophyllales
inferred← citeshttps://doi.org/10.1016/b978-0-12-819166-8.00066-9openalex-snapshot
Prehistoric Wetlands
inferred← citeshttps://doi.org/10.1016/bs.abr.2017.11.016openalex-snapshot
Plastome Phylogenetics: 30 Years of Inferences Into Plant Evolution
inferred← citeshttps://doi.org/10.1016/j.agee.2023.108740openalex-snapshot
Effect of spontaneous vegetation on beneficial arthropods in Mediterranean vineyards
inferred← citeshttps://doi.org/10.1016/j.flora.2012.03.001openalex-snapshot
Contributions to the floral anatomy of Juncaceae (Poales – Monocotyledons)
inferred← citeshttps://doi.org/10.1016/j.flora.2020.151538openalex-snapshot
Androecium and gynoecium anatomy of Bromeliaceae species
inferred← citeshttps://doi.org/10.1016/j.flora.2020.151691openalex-snapshot
Diversity and evolutionary trends of the ovary and ovule in Bromeliaceae
inferred← citeshttps://doi.org/10.1016/j.flora.2023.152238openalex-snapshot
Understanding the seedling development in sedge species (Cyperaceae, Poales) from micromorphological and anatomical perspectives
inferred← citeshttps://doi.org/10.1016/j.gene.2012.03.061openalex-snapshot
Characterization of the chloroplast genome sequence of oil palm (Elaeis guineensis Jacq.)
inferred← citeshttps://doi.org/10.1016/j.gene.2013.08.067openalex-snapshot
Transcriptome sequencing and phylogenetic analysis of floral and leaf MIKCC MADS-box and R2R3 MYB transcription factors from the monocot Iris fulva
inferred← citeshttps://doi.org/10.1016/j.gene.2016.11.038openalex-snapshot
Complete plastid genome sequence of goosegrass (Eleusine indica) and comparison with other Poaceae
inferred← citeshttps://doi.org/10.1016/j.pld.2022.11.003openalex-snapshot
Insights into cryptic speciation of quillworts in China
inferred← citeshttps://doi.org/10.1016/j.revpalbo.2014.08.017openalex-snapshot
Fossil Araceae from the Upper Cretaceous of Patagonia, Argentina, with implications on the origin of free-floating aquatic aroids
inferred← citeshttps://doi.org/10.1016/j.ympev.2012.01.009openalex-snapshot
Phylogenetic insights into the correlates of dioecy in meadow-rues (Thalictrum, Ranunculaceae)
inferred← citeshttps://doi.org/10.1016/j.ympev.2012.05.010openalex-snapshot
Complete cpDNA genome sequence of Smilax china and phylogenetic placement of Liliales – Influences of gene partitions and taxon sampling
inferred← citeshttps://doi.org/10.1016/j.ympev.2013.10.010openalex-snapshot
Adaptive radiation, correlated and contingent evolution, and net species diversification in Bromeliaceae
inferred← citeshttps://doi.org/10.1016/j.ympev.2014.02.017openalex-snapshot
Phylogenomics of the plant family Araceae
inferred← citeshttps://doi.org/10.1016/j.ympev.2014.11.003openalex-snapshot
Deep phylogenetic incongruence in the angiosperm clade Rosidae
inferred← citeshttps://doi.org/10.1016/j.ympev.2015.10.003openalex-snapshot
Utilizing next-generation sequencing to resolve the backbone of the Core Goodeniaceae and inform future taxonomic and floral form studies
inferred← citeshttps://doi.org/10.1016/j.ympev.2015.12.015openalex-snapshot
Nuclear phylogenomics of the palm subfamily Arecoideae (Arecaceae)
inferred← citeshttps://doi.org/10.1016/j.ympev.2016.02.022openalex-snapshot
Multilocus phylogeny and phylogenomics of Eriochrysis P. Beauv. (Poaceae–Andropogoneae): Taxonomic implications and evidence of interspecific hybridization
inferred← citeshttps://doi.org/10.1016/j.ympev.2016.08.011openalex-snapshot
Evolutionary history of chloridoid grasses estimated from 122 nuclear loci
inferred← citeshttps://doi.org/10.1016/j.ympev.2016.12.031openalex-snapshot
First plastid phylogenomic study reveals potential cyto-nuclear discordance in the evolutionary history of Ficus L. (Moraceae)
inferred← citeshttps://doi.org/10.1016/j.ympev.2019.106540openalex-snapshot
Phylogenomics of Orchidaceae based on plastid and mitochondrial genomes
inferred← citeshttps://doi.org/10.1016/j.ympev.2019.106699openalex-snapshot
Phylogeny of Diplazium (Athyriaceae) revisited: Resolving the backbone relationships based on plastid genomes and phylogenetic tree space analysis
inferred← citeshttps://doi.org/10.1016/j.ympev.2021.107171openalex-snapshot
Plastid genomes and phylogenomics of liverworts (Marchantiophyta): Conserved genome structure but highest relative plastid substitution rate in land plants
inferred← citeshttps://doi.org/10.1016/j.ympev.2023.107961openalex-snapshot
Plastid phylogenomics of the tribe potentilleae (Rosaceae)
inferred← citeshttps://doi.org/10.1016/j.ympev.2024.108184openalex-snapshot
Phylogenomics resolves the backbone of Poales and identifies signals of hybridization and polyploidy
inferred← citeshttps://doi.org/10.1016/j.ympev.2025.108327openalex-snapshot
Phylogenomic and morphological evidence supports the reinstatement of the bamboo genus Clavinodum from Oligostachyum (Poaceae: Bambusoideae)
inferred← citeshttps://doi.org/10.1017/9781139939867.001openalex-snapshot
Introduction: Wilting Leaves and Rotting Branches
inferred← citeshttps://doi.org/10.1017/cbo9781139002950.002openalex-snapshot
A well-supported phylogenetic framework for the monocot order Alismatales reveals multiple losses of the plastid NADH dehydrogenase complex and a strong long-branch effect
inferred← citeshttps://doi.org/10.1017/cbo9781139002950.015openalex-snapshot
Contrasting patterns of support among plastid genes and genomes for major clades of the monocotyledons
inferred← citeshttps://doi.org/10.1017/s0960258521000209openalex-snapshot
Relationship of the lateral embryo (in grasses) to other monocot embryos: a status up-grade
inferred← citeshttps://doi.org/10.1038/nature11241openalex-snapshot
The banana (Musa acuminata) genome and the evolution of monocotyledonous plants
inferred← citeshttps://doi.org/10.1038/s41467-023-38836-4openalex-snapshot
The genome of Acorus deciphers insights into early monocot evolution
inferred← citeshttps://doi.org/10.1038/s41597-026-06640-6openalex-snapshot
Chromosome-level genome assembly of narrow-leaf bur-reed (Sparganium angustifolium Michx., Typhaceae)
inferred← citeshttps://doi.org/10.1038/srep09040openalex-snapshot
The location and translocation of ndh genes of chloroplast origin in the Orchidaceae family
inferred← citeshttps://doi.org/10.1038/srep28598openalex-snapshot
Gibberellin deficiency is responsible for shy-flowering nature of Epipremnum aureum
inferred← citeshttps://doi.org/10.1071/bt14138openalex-snapshot
Synchronous monoecy in Ecdeiocoleaceae (Poales), in Western Australia
inferred← citeshttps://doi.org/10.1080/11263504.2020.1845846openalex-snapshot
Insect pollination in temperate sedges? A case study in Rhynchospora alba (Cyperaceae)
inferred← citeshttps://doi.org/10.1080/14772000.2014.890137openalex-snapshot
Phylogenetic relationships in the grass family (Poaceae) based on the nuclear single copy locus topoisomerase 6 compared with chloroplast DNA
inferred← citeshttps://doi.org/10.1080/17550874.2012.745909openalex-snapshot
Making next-generation sequencing work for you: approaches and practical considerations for marker development and phylogenetics
inferred← citeshttps://doi.org/10.1080/23802359.2019.1572475openalex-snapshot
The complete chloroplast genome of Eriocaulon sexangulare (Eriocaulaceae)
inferred← citeshttps://doi.org/10.1080/23802359.2019.1638840openalex-snapshot
Characterization of the complete chloroplast genome of Malus baccata var. xiaojinensis
inferred← citeshttps://doi.org/10.1080/23802359.2023.2183070openalex-snapshot
Complete chloroplast genome of Isoetes orientalis (Isoetaceae), an endangered quillwort from China
inferred← citeshttps://doi.org/10.1086/666664openalex-snapshot
Floral Anatomy of Xyrids (Poales): Contributions to Their Reproductive Biology, Taxonomy, and Phylogeny
inferred← citeshttps://doi.org/10.1086/673247openalex-snapshot
Experimental Evidence of Insect Pollination in Juncaceae, a Primarily Wind-Pollinated Family
inferred← citeshttps://doi.org/10.1086/674317openalex-snapshot
Evolution and Development of the Spikelet and Flower of Rhynchospora (Cyperaceae)
inferred← citeshttps://doi.org/10.1086/676675openalex-snapshot
Angiosperm Phylogeny Based on 18S/26S rDNA Sequence Data: Constructing a Large Data Set Using Next-Generation Sequence Data
inferred← citeshttps://doi.org/10.1086/680401openalex-snapshot
Anther Wall Development, Microsporogenesis, and Microgametogenesis inAbolbodaandOrectanthe: Contributions to the Embryology of Xyridaceae (Poales)
inferred← citeshttps://doi.org/10.1086/689617openalex-snapshot
Ovule, Fruit, and Seed Development ofOrectanthe sceptrumand Its Systematic Relevance to Xyridaceae (Poales)
inferred← citeshttps://doi.org/10.1086/726005openalex-snapshot
Mitochondrial Genome Sequencing and Analysis of the Invasive Microstegium vimineum: A Resource for Systematics, Invasion History, and Management
inferred← citeshttps://doi.org/10.1093/aob/mcab100openalex-snapshot
Floral development and vasculature in Eriocaulon (Eriocaulaceae) provide insights into the evolution of Poales
inferred← citeshttps://doi.org/10.1093/aob/mcaf167openalex-snapshot
Hygroscopic awns and inflorescence architecture in a wind-pollinated Australian monocot: functional convergence with grasses
inferred← citeshttps://doi.org/10.1093/aob/mcaf311openalex-snapshot
Between wind and visitors? Insights into floral anatomy, taxonomy and reproductive biology in Cryptangieae (Cyperaceae)
inferred← citeshttps://doi.org/10.1093/aob/mcs124openalex-snapshot
Self-sterility in flowering plants: preventing self-fertilization increases family diversification rates
inferred← citeshttps://doi.org/10.1093/aob/mct264openalex-snapshot
Resolving ancient radiations: can complete plastid gene sets elucidate deep relationships among the tropical gingers (Zingiberales)?
inferred← citeshttps://doi.org/10.1093/aob/mcy025openalex-snapshot
Fusoid cells in the grass family Poaceae (Poales): a developmental study reveals homologies and suggests new insights into their functional role in young leaves
inferred← citeshttps://doi.org/10.1093/aobpla/plv046openalex-snapshot
Plastid phylogenomics of the cool-season grass subfamily: clarification of relationships among early-diverging tribes
inferred← citeshttps://doi.org/10.1093/botlinnean/boaa052openalex-snapshot
Rapid diversification rates in Amazonian Chrysobalanaceae inferred from plastid genome phylogenetics
inferred← citeshttps://doi.org/10.1093/botlinnean/boab031openalex-snapshot
Inferences on gynoecium evolution in Xyris (Xyridaceae, Poales) based on floral anatomy and development
inferred← citeshttps://doi.org/10.1093/botlinnean/boad042openalex-snapshot
Can flowers help to disentangle the Vriesea oligantha complex (Bromeliaceae: Tillandsioideae)? Taxonomic implications and contributions to the floral anatomy and biology of Stigmatodon
inferred← citeshttps://doi.org/10.1093/botlinnean/boad067openalex-snapshot
Inherit the wind: evolution of reproductive traits in Cyperaceae
inferred← citeshttps://doi.org/10.1093/botlinnean/boy026openalex-snapshot
A phylogenetic analysis of the genus Aloe (Asphodelaceae) in Madagascar and the Mascarene Islands
inferred← citeshttps://doi.org/10.1093/botlinnean/boz039openalex-snapshot
Ecological niche modelling and genetic diversity of Anomochloa marantoidea (Poaceae): filling the gaps for conservation in the earliest-diverging grass subfamily
inferred← citeshttps://doi.org/10.1093/botlinnean/boz060openalex-snapshot
Plastome phylogenomics of Poaceae: alternate topologies depend on alignment gaps
inferred← citeshttps://doi.org/10.1093/botlinnean/boz111openalex-snapshot
Seed development and its relationship to fruit structure in species of Bromelioideae (Bromeliaceae) with fleshy fruits
inferred← citeshttps://doi.org/10.1093/gbe/evac183openalex-snapshot
Phylotranscriptomic Analyses of Mycoheterotrophic Monocots Show a Continuum of Convergent Evolutionary Changes in Expressed Nuclear Genes From Three Independent Nonphotosynthetic Lineages
inferred← citeshttps://doi.org/10.1093/gbe/evv134openalex-snapshot
The Highly Reduced Plastome of MycoheterotrophicSciaphila(Triuridaceae) Is Colinear with Its Green Relatives and Is under Strong Purifying Selection
inferred← citeshttps://doi.org/10.1093/gbe/evw060openalex-snapshot
A phylogenomic assessment of ancient polyploidy and genome evolution across the Poales
inferred← citeshttps://doi.org/10.1093/gbe/evy189openalex-snapshot
Mobile Elements Shape Plastome Evolution in Ferns
inferred← citeshttps://doi.org/10.1093/gbe/evz092openalex-snapshot
Ancient Polyploidy and Genome Evolution in Palms
inferred← citeshttps://doi.org/10.1093/molbev/msw031openalex-snapshot
Evolutionary Dynamics of Floral Homeotic Transcription Factor Protein–Protein Interactions
inferred← citeshttps://doi.org/10.1093/sysbio/syt072openalex-snapshot
Molecular Dating, Evolutionary Rates, and the Age of the Grasses
inferred← citeshttps://doi.org/10.1101/2020.06.22.165738openalex-snapshot
Wetland plant evolutionary history influences soil and endophyte microbial community composition
inferred← citeshttps://doi.org/10.1101/2023.02.10.527995openalex-snapshot
Mitochondrial genome sequencing and analysis of the invasive Microstegium vimineum : a resource for systematics, invasion history, and management
inferred← citeshttps://doi.org/10.1101/2024.11.06.622220openalex-snapshot
Genomes of Poaceae sisters reveal key metabolic innovations preceding the evolution of grasses
inferred← citeshttps://doi.org/10.1104/pp.18.00298openalex-snapshot
Commelinid Monocotyledon Lignins Are Acylated by p-Coumarate
inferred← citeshttps://doi.org/10.1111/1755-0998.12246openalex-snapshot
Genome skimming by shotgun sequencing helps resolve the phylogeny of a pantropical tree family
inferred← citeshttps://doi.org/10.1111/1755-0998.12487openalex-snapshot
Phylogenetic marker development for target enrichment from transcriptome and genome skim data: the pipeline and its application in southern African Oxalis (Oxalidaceae)
inferred← citeshttps://doi.org/10.1111/1755-0998.13562openalex-snapshot
Chromosome‐level de novo genome assembly and whole‐genome resequencing of the threatened species Acanthochlamys bracteata (Velloziaceae) provide insights into alpine plant divergence in a biodiversity hotspot
inferred← citeshttps://doi.org/10.1111/1755-0998.13850openalex-snapshot
Genomic analysis of the emergent aquatic plant Sparganium stoloniferum provides insights into its clonality, local adaptation and demographic history
inferred← citeshttps://doi.org/10.1111/bij.12551openalex-snapshot
Phylogenomic analyses of species relationships in the genusSabal(Arecaceae) using targeted sequence capture
inferred← citeshttps://doi.org/10.1111/boj.12152openalex-snapshot
Ovule, fruit and seed development inAbolboda(Xyridaceae, Poales): implications for taxonomy and phylogeny
inferred← citeshttps://doi.org/10.1111/boj.12160openalex-snapshot
A revised evolutionary history of Poales: origins and diversification
inferred← citeshttps://doi.org/10.1111/boj.12265openalex-snapshot
Development of ovule, fruit and seed of X yris (Xyridaceae, Poales) and taxonomic considerations
inferred← citeshttps://doi.org/10.1111/boj.12275openalex-snapshot
Photosynthetic pathways in Bromeliaceae: phylogenetic and ecological significance of CAM and C 3 based on carbon isotope ratios for 1893 species
inferred← citeshttps://doi.org/10.1111/boj.12385openalex-snapshot
An update of the Angiosperm Phylogeny Group classification for the orders and families of flowering plants: APG IV
inferred← citeshttps://doi.org/10.1111/boj.12431openalex-snapshot
Advances in and perspectives on evolution in Bromeliaceae
inferred← citeshttps://doi.org/10.1111/cla.12133openalex-snapshot
Plastid phylogenomics and molecular evolution of Alismatales
inferred← citeshttps://doi.org/10.1111/cla.12153openalex-snapshot
Phylogenomics and historical biogeography of the monocot order Liliales: out of Australia and through Antarctica
inferred← citeshttps://doi.org/10.1111/j.1095-8339.2012.01267.xopenalex-snapshot
Flower development and vasculature in Xyris grandis (Xyridaceae, Poales); a case study for examining petal diversity in monocot flowers with a double perianth
inferred← citeshttps://doi.org/10.1111/j.1095-8339.2012.01283.xopenalex-snapshot
Morphological evolution in the graminid clade: comparative floral anatomy of the grass relatives Flagellariaceae and Joinvilleaceae
inferred← citeshttps://doi.org/10.1111/j.1096-0031.2012.00418.xopenalex-snapshot
Plastid genomes and deep relationships among the commelinid monocot angiosperms
inferred← citeshttps://doi.org/10.1111/jbi.12486openalex-snapshot
Ancient Gondwana break‐up explains the distribution of the mycoheterotrophic family Corsiaceae (Liliales)
inferred← citeshttps://doi.org/10.1111/jbi.12711openalex-snapshot
Correlates of range size variation in the Australian seed‐plant flora
inferred← citeshttps://doi.org/10.1111/jse.12526openalex-snapshot
Revisiting the phylogeny of Dipsacales: New insights from phylogenomic analyses of complete plastomic sequences
inferred← citeshttps://doi.org/10.1111/jse.12579openalex-snapshot
Evaluating character partitioning and molecular models in plastid phylogenomics at low taxonomic levels: A case study using Amphilophium (Bignonieae, Bignoniaceae)
inferred← citeshttps://doi.org/10.1111/jse.12757openalex-snapshot
A new classification of Cyperaceae (Poales) supported by phylogenomic data
inferred← citeshttps://doi.org/10.1111/mec.12870openalex-snapshot
Genomics of the divergence continuum in an African plant biodiversity hotspot, I: drivers of population divergence in Restio capensis (Restionaceae)
inferred← citeshttps://doi.org/10.1111/njb.01800openalex-snapshot
Anatomy of vegetative organs, inflorescence axis and pedicel in the Neoregelia bahiana complex (Bromeliaceae): taxonomic and ecological importance
inferred← citeshttps://doi.org/10.1111/njb.04121openalex-snapshot
Pollination biology of a rare serpentine plant, Japonolirion osense (Petrosaviaceae)
inferred← citeshttps://doi.org/10.1111/nph.13331openalex-snapshot
On the complexity of triggering evolutionary radiations
inferred← citeshttps://doi.org/10.1111/nph.13471openalex-snapshot
Analysis of the giant genomes of F ritillaria ( L iliaceae) indicates that a lack of DNA removal characterizes extreme expansions in genome size
inferred← citeshttps://doi.org/10.1111/nph.13617openalex-snapshot
Plastid genomes reveal support for deep phylogenetic relationships and extensive rate variation among palms and other commelinid monocots
inferred← citeshttps://doi.org/10.1111/ppl.70463openalex-snapshot
Bulliform Cell‐Induced Leaf Curling Contributes to Water Loss and Water Potential Regulation of Bamboos During Dry Season
inferred← citeshttps://doi.org/10.1111/tpj.12715openalex-snapshot
Evolutionary divergence of β–expansin structure and function in grasses parallels emergence of distinctive primary cell wall traits
inferred← citeshttps://doi.org/10.1126/science.adv0443openalex-snapshot
Genomes of Poaceae relatives reveal key metabolic innovations preceding the evolution of grasses
inferred← citeshttps://doi.org/10.1139/b09-093openalex-snapshot
Inference of phylogenetic relationships among the subfamilies of grasses (Poaceae: Poales) using meso-scale exemplar-based sampling of the plastid genome
inferred← citeshttps://doi.org/10.1186/1471-2164-12-211openalex-snapshot
Building a model: developing genomic resources for common milkweed (Asclepias syriaca) with low coverage genome sequencing
inferred← citeshttps://doi.org/10.1186/2041-2223-5-1openalex-snapshot
DNA fingerprinting in botany: past, present, future
inferred← citeshttps://doi.org/10.1186/s12862-018-1160-yopenalex-snapshot
Phylogenomics and barcoding of Panax: toward the identification of ginseng species
inferred← citeshttps://doi.org/10.1186/s12862-025-02396-6openalex-snapshot
Plastome phylogenomics of the diverse neotropical orchid genus Lepanthes with emphasis on subgenus Marsipanthes (Pleurothallidinae: Orchidaceae)
inferred← citeshttps://doi.org/10.1186/s12864-017-3904-2openalex-snapshot
Molecular dating of phylogenetic divergence between Urochloa species based on complete chloroplast genomes
inferred← citeshttps://doi.org/10.1186/s12864-017-4303-4openalex-snapshot
Identification of differentially expressed genes in flower, leaf and bulb scale of Lilium oriental hybrid ‘Sorbonne’ and putative control network for scent genes
inferred← citeshttps://doi.org/10.1186/s12864-019-5886-8openalex-snapshot
RNA-Seq analysis of soft rush (Juncus effusus): transcriptome sequencing, de novo assembly, annotation, and polymorphism identification
inferred← citeshttps://doi.org/10.1186/s12870-015-0587-1openalex-snapshot
Complete chloroplast genome sequence of MD-2 pineapple and its comparative analysis among nine other plants from the subclass Commelinidae
inferred← citeshttps://doi.org/10.1186/s12915-024-01890-5openalex-snapshot
Unprecedented variation pattern of plastid genomes and the potential role in adaptive evolution in Poales
inferred← citeshttps://doi.org/10.1186/s13020-018-0164-2openalex-snapshot
Complete chloroplast genome of the medicinal plant Amomum compactum: gene organization, comparative analysis, and phylogenetic relationships within Zingiberales
inferred← citeshttps://doi.org/10.1186/s13104-017-3077-8openalex-snapshot
The complete chloroplast genome sequence of Asian Palmyra palm (Borassus flabellifer)
inferred← citeshttps://doi.org/10.1206/3860.1openalex-snapshot
Two New Species ofPulvillophylusfrom Western Australia (Insecta: Hemiptera: Miridae: Phylinae: Cremnorrhinini)
inferred← citeshttps://doi.org/10.12705/631.1openalex-snapshot
Phylogeny of the restiid clade (Poales) and implications for the classification of Anarthriaceae, Centrolepidaceae and Australian Restionaceae
inferred← citeshttps://doi.org/10.12705/643.9openalex-snapshot
A genus‐level phylogenetic linear sequence of monocots
inferred← citeshttps://doi.org/10.12705/653.12openalex-snapshot
The identity and application of Coletia madida and notes on the typification of Mayacaceae
inferred← citeshttps://doi.org/10.12705/673.5openalex-snapshot
Nuclear genes, matK and the phylogeny of the Poales
inferred← citeshttps://doi.org/10.1360/ssv-2020-0345openalex-snapshot
Significance of plant taxonomy in Chinese material medica resources: the changes of family and genus category and standardization of scientific names in Chinese Pharmacopoeia
inferred← citeshttps://doi.org/10.1371/journal.pone.0048995openalex-snapshot
Reference-Free Comparative Genomics of 174 Chloroplasts
inferred← citeshttps://doi.org/10.1371/journal.pone.0067350openalex-snapshot
The Complete Chloroplast Genome of Banana (Musa acuminata, Zingiberales): Insight into Plastid Monocotyledon Evolution
inferred← citeshttps://doi.org/10.1371/journal.pone.0068180openalex-snapshot
Comparative Genome Analysis and Phylogenetic Relationship of Order Liliales Insight from the Complete Plastid Genome Sequences of Two Lilies (Lilium longiflorum and Alstroemeria aurea)
inferred← citeshttps://doi.org/10.1371/journal.pone.0106459openalex-snapshot
At Least 23 Genera Instead of One: The Case of Iris L. s.l. (Iridaceae)
inferred← citeshttps://doi.org/10.1371/journal.pone.0142215openalex-snapshot
Seven New Complete Plastome Sequences Reveal Rampant Independent Loss of the ndh Gene Family across Orchids and Associated Instability of the Inverted Repeat/Small Single-Copy Region Boundaries
inferred← citeshttps://doi.org/10.1371/journal.pone.0163218openalex-snapshot
The First Complete Plastid Genome from Joinvilleaceae (J. ascendens; Poales) Shows Unique and Unpredicted Rearrangements
inferred← citeshttps://doi.org/10.1371/journal.pone.0198513openalex-snapshot
Not stealing from the treasure chest (or just a bit): Analyses on plant derived writing supports and non-invasive DNA sampling
inferred← citeshttps://doi.org/10.1371/journal.pone.0221423openalex-snapshot
Understanding evolution in Poales: Insights from Eriocaulaceae plastome
inferred← citeshttps://doi.org/10.1534/g3.119.400214openalex-snapshot
Transcriptome Analysis Reveals Unique Relationships AmongEleusineSpecies and Heritage ofEleusine coracana
inferred← citeshttps://doi.org/10.1590/0001-3765201520140071openalex-snapshot
Leaf and inflorescence axis anatomy of Brazilian species of Rapateoideae (Rapateaceae, Poales)
inferred← citeshttps://doi.org/10.1590/0102-33062020abb0236openalex-snapshot
Breaking the misconception of a dry and lifeless semiarid region: the diversity and distribution of aquatic flora in wetlands of the Brazilian Northeast
inferred← citeshttps://doi.org/10.1590/1678-4685-gmb-2018-0371openalex-snapshot
RNA editing in the chloroplast of Asian Palmyra palm (Borassus flabellifer)
inferred← citeshttps://doi.org/10.1590/2175-7860201566203openalex-snapshot
Overview of the systematics and diversity of Poales in the Neotropics with emphasis on the Brazilian flora
inferred← citeshttps://doi.org/10.1590/2175-7860201566204openalex-snapshot
An overview on pollination of the Neotropical Poales
inferred← citeshttps://doi.org/10.1590/2175-7860201566210openalex-snapshot
Revisiting Mayacaceae Kunth towards to future perspectives in the family
inferred← citeshttps://doi.org/10.1590/2175-7860202071102openalex-snapshot
Polinização por vibração em Saxofridericia (Poales: Rapateaceae): o caso de S. brasiliensis e abelhas Euglossini
inferred← citeshttps://doi.org/10.1590/2179-8087.170764openalex-snapshot
Are Seeds of Genipa americana L. (Rubiaceae) Tolerance to Water Submersion?
inferred← citeshttps://doi.org/10.1590/2236-8906-78/2015openalex-snapshot
Anatomia floral de Aechmea distichantha Lem. e Canistropsis billbergioides (Schult. & Schult.f) Leme (Bromeliaceae)
inferred← citeshttps://doi.org/10.17520/biods.2015052openalex-snapshot
Families and genera of Chinese angiosperms: a synoptic classification based on APG III
inferred← citeshttps://doi.org/10.22146/jtbb.76956openalex-snapshot
Region of Nuclear Ribosomal DNA (ITS2) and Chloroplast DNA (rbcL and trnL-F) as A Suitable DNA Barcode for Identification of Zingiber loerzingii Valeton From North Sumatera, Indonesia
inferred← citeshttps://doi.org/10.3100/hpib.v21iss1.2016.n9openalex-snapshot
Morphology and Anatomy ofGuacamaya superba(Rapateaceae) and Schoenocephalieae with Notes on the Natural History of theFlor de inírida
inferred← citeshttps://doi.org/10.3103/s0095452721010096openalex-snapshot
Application of 5S Ribosomal DNA for Molecular Taxonomy of Subtribe Loliinae (Poaceae)
inferred← citeshttps://doi.org/10.3159/torrey-d-11-00027.1openalex-snapshot
On the taxonomic value of the anatomical structure of vegetative organs and inflorescence axis of Abolboda species (Xyridaceae – Poales)1
inferred← citeshttps://doi.org/10.3389/fpls.2013.00250openalex-snapshot
Early inflorescence development in the grasses (Poaceae)
inferred← citeshttps://doi.org/10.3389/fpls.2016.01993openalex-snapshot
Phylogenomics and Plastome Evolution of Tropical Forest Grasses (Leptaspis, Streptochaeta: Poaceae)
inferred← citeshttps://doi.org/10.3389/fpls.2021.699226openalex-snapshot
Phylogeny, Age, and Evolution of Tribe Lilieae (Liliaceae) Based on Whole Plastid Genomes
inferred← citeshttps://doi.org/10.3389/fpls.2021.710383openalex-snapshot
The Streptochaeta Genome and the Evolution of the Grasses
inferred← citeshttps://doi.org/10.3389/fpls.2021.813915openalex-snapshot
Flower and Spikelet Construction in Rapateaceae (Poales)
inferred← citeshttps://doi.org/10.3389/fpls.2021.824672openalex-snapshot
Organelle Phylogenomics and Extensive Conflicting Phylogenetic Signals in the Monocot Order Poales
inferred← citeshttps://doi.org/10.3389/fpls.2022.876779openalex-snapshot
Phylogenomic resolution of order- and family-level monocot relationships using 602 single-copy nuclear genes and 1375 BUSCO genes
inferred← citeshttps://doi.org/10.3389/fpls.2022.918155openalex-snapshot
Untying the Gordian knot of plastid phylogenomic conflict: A case from ferns
inferred← citeshttps://doi.org/10.3389/fpls.2025.1647198openalex-snapshot
Interactive effects of life cycle and monocot-dicot lineage on genome size–trait relationships in angiosperms: a phylogenetically informed analysis
inferred← citeshttps://doi.org/10.3390/d18030174openalex-snapshot
Plastid Genome Characterization and Development of Plastid and Nuclear SNP Markers for Juncus decipiens (Juncaceae)
inferred← citeshttps://doi.org/10.3390/genes17030353openalex-snapshot
Genome-Wide Identification and Expression Analysis of the WSD Gene Family in Wheat
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