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Phylogeny of the restiid clade (Poales) and implications for the classification of Anarthriaceae, Centrolepidaceae and Australian Restionaceae
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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.20011120111openalex-snapshot
Restionaceae seedlings: Morphology, anatomy and systematic implications
inferredcites →https://doi.org/10.1002/j.1537-2197.1988.tb11258.xopenalex-snapshot
MEGAGAMETOPHYTE AND NUCELLUS IN RESTIONACEAE AND FLAGELLARIACEAE
inferredcites →https://doi.org/10.1002/j.1537-2197.1990.tb13546.xopenalex-snapshot
CLADISTIC ANALYSIS OF PATTERNS OF ENDOTHECIAL THICKENINGS IN THE POALES/RESTIONALES
inferredcites →https://doi.org/10.1002/j.1537-2197.1993.tb15391.xopenalex-snapshot
The megagametophyte in Anarthria (Anarthriaceae, Poales) and its implications for the phylogeny of the Poales
inferredcites →https://doi.org/10.1006/bojl.2000.0368openalex-snapshot
Vicariance, climate change, anatomy and phylogeny of Restionaceae
inferredcites →https://doi.org/10.1007/1-4020-5906-x_19openalex-snapshot
Role of Root Clusters in Phosphorus Acquisition and Increasing Biological Diversity in Agriculture
inferredcites →https://doi.org/10.1007/978-3-642-61663-1openalex-snapshot
The Families of the Monocotyledons
inferredcites →https://doi.org/10.1007/978-3-642-68935-2_14openalex-snapshot
Strategies for Maximizing Nutrient Uptake in Two Mediterranean Ecosystems of Low Nutrient Status
inferredcites →https://doi.org/10.1007/978-94-009-8629-9_15openalex-snapshot
Three old southern families-Myrtaceae, Proteaceae and Restionaceae
inferredcites →https://doi.org/10.1007/bf02426962openalex-snapshot
Phylogenetic affinities of the grasses to other monocots as revealed by molecular analysis of chloroplast DNA
inferredcites →https://doi.org/10.1007/bf02860714openalex-snapshot
Mechanisms for enhancing nutrient uptake in plants, with particular reference to mediterranean South Africa and Western Australia
inferredcites →https://doi.org/10.1007/pl00013995openalex-snapshot
Floral Ontogenetic Evidence in Support of the Willdenowia Clade of South African Restionaceae
inferredcites →https://doi.org/10.1007/s00299-001-0399-7openalex-snapshot
Regeneration and molecular characterization of intergeneric somatic hybrids between Citrus reticulata and Poncirus trifoliata
inferredcites →https://doi.org/10.1007/s006060200021openalex-snapshot
Ontogeny and evolution of the flowers of South African Restionaceae with special emphasis on the gynoecium
inferredcites →https://doi.org/10.1007/s12225-011-9259-yopenalex-snapshot
Summary of recent systems of angiosperm classification
inferredcites →https://doi.org/10.1016/j.ympev.2004.12.006openalex-snapshot
Taxon sampling effects in molecular clock dating: An example from the African Restionaceae
inferredcites →https://doi.org/10.1016/j.ympev.2007.02.030openalex-snapshot
A congruent molecular signature of vicariance across multiple plant lineages
inferredcites →https://doi.org/10.1016/j.ympev.2007.04.001openalex-snapshot
The relative performance of indel-coding methods in simulations
inferredcites →https://doi.org/10.1016/s0031-9422(97)00139-8openalex-snapshot
Flavonoid evidence and the classification of the anarthriaceae within the poales
inferredcites →https://doi.org/10.1016/s0031-9422(98)00050-8openalex-snapshot
Flavonoid patterns and the revised classification of Australian Restionaceae
inferredcites →https://doi.org/10.1071/9780643090149openalex-snapshot
Monocots: Systematics and Evolution
inferredcites →https://doi.org/10.1071/bt01089openalex-snapshot
Evolutionary strategies for reproduction and dispersal in African Restionaceae
inferredcites →https://doi.org/10.1071/bt9760281openalex-snapshot
Alexgeorgea , a bizarre new genus of Restionaceae from Western Australia
inferredcites →https://doi.org/10.1071/sb9900751openalex-snapshot
The species of Alexgeorgea , a Western Australian genus of the restionaceae
inferredcites →https://doi.org/10.1071/sb9920227openalex-snapshot
The gynocecia of Australian restionaceae: Morphology, anatomy and systematic implications
inferredcites →https://doi.org/10.1080/00173134.1977.11864634openalex-snapshot
Pollen Morphology of Some Members of the Restionaceae and Related Families, with Notes on the Fossil Record
inferredcites →https://doi.org/10.1080/00173136609430033openalex-snapshot
On the Pollen Morphology of the Centrolepidaceae, Restionaceae and Flagellariaceae, with Special Reference to Taxonomy
inferredcites →https://doi.org/10.1080/00173136709432845openalex-snapshot
Apertural Types in Pollen of the Restionaceae and Flagellariaceae
inferredcites →https://doi.org/10.1080/00173138509429917openalex-snapshot
Notes on the Pollen Morphology and Phylogeny Restionales and Poales
inferredcites →https://doi.org/10.1080/09670260802207530openalex-snapshot
Building trees of algae: some advances in phylogenetic and evolutionary analysis
inferredcites →https://doi.org/10.1080/106351501753462876openalex-snapshot
A Likelihood Approach to Estimating Phylogeny from Discrete Morphological Character Data
inferredcites →https://doi.org/10.1080/10635150390235520openalex-snapshot
A Simple, Fast, and Accurate Algorithm to Estimate Large Phylogenies by Maximum Likelihood
inferredcites →https://doi.org/10.1080/10635150590923317openalex-snapshot
Intraspecific Variability and Timing in Ancestral Ecology Reconstruction: A Test Case from the Cape Flora
inferredcites →https://doi.org/10.1080/10635150701397643openalex-snapshot
Detecting and Overcoming Systematic Errors in Genome-Scale Phylogenies
inferredcites →https://doi.org/10.1080/10635150801888871openalex-snapshot
Resolving an Ancient, Rapid Radiation in Saxifragales
inferredcites →https://doi.org/10.1086/526467openalex-snapshot
A Phylogeny for the African Restionaceae and New Perspectives on Morphology’s Role in Generating Complete Species Phylogenies for Large Clades
inferredcites →https://doi.org/10.1093/aob/mcr213openalex-snapshot
Diversity, phylogeny, and evolution in the monocotyledons
inferredcites →https://doi.org/10.1093/molbev/msn083openalex-snapshot
jModelTest: Phylogenetic Model Averaging
inferredcites →https://doi.org/10.1093/nar/22.22.4673openalex-snapshot
CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice
inferredcites →https://doi.org/10.1093/nar/gki352openalex-snapshot
PHYML Online--a web server for fast maximum likelihood-based phylogenetic inference
inferredcites →https://doi.org/10.1093/sysbio/49.2.369openalex-snapshot
Gaps as Characters in Sequence-Based Phylogenetic Analyses
inferredcites →https://doi.org/10.1093/sysbio/sys001openalex-snapshot
Overcoming Deep Roots, Fast Rates, and Short Internodes to Resolve the Ancient Rapid Radiation of Eupolypod II Ferns
inferredcites →https://doi.org/10.1093/sysbio/sys005openalex-snapshot
Searching for Ancestral Areas and Artifactual Centers of Origin in Biogeography: with Comment on East–West Patterns Across Southern Australia
inferredcites →https://doi.org/10.1098/rspb.2000.1130openalex-snapshot
Early–branching or fast–evolving eukaryotes? An answer based on slowly evolving positions
inferredcites →https://doi.org/10.1098/rstb.2004.1528openalex-snapshot
Radiation of the Australian flora: what can comparisons of molecular phylogenies across multiple taxa tell us about the evolution of diversity in present–day communities?
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.0908-8857.2004.03297.xopenalex-snapshot
Glacial history and colonization of Europe by the blue tit Parus caeruleus
inferredcites →https://doi.org/10.1111/j.1095-8339.1992.tb00282.xopenalex-snapshot
The structure and evolution of the female flower of the African Restionaceae
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.1096-0031.2005.00059.xopenalex-snapshot
A review of long‐branch attraction
inferredcites →https://doi.org/10.1111/j.1438-8677.1962.tb02521.xopenalex-snapshot
17. Ulrich Hamann: Beitrag zur Embryologie der Centrolepidaceae mit Bemerkungen über den Bau der Blüten und Blütenstände und die systematische Stellung der Familie
inferredcites →https://doi.org/10.1111/j.1469-8137.2004.01032.xopenalex-snapshot
Evolution of zygomorphy in monocot flowers: iterative patterns and developmental constraints
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/10.1146/annurev.ecolsys.36.102403.135635openalex-snapshot
Evolutionary History of Poales
inferredcites →https://doi.org/10.1600/036364405775097842openalex-snapshot
Molecular Phylogeny and Generic Delimitation in the Elegia Group (Restionaceae, South Africa) Based on a Complete Taxon Sampling and Four Chloroplast DNA Regions
inferredcites →https://doi.org/10.1663/0006-8101(2004)069[0377:sabosb]2.0.co;2openalex-snapshot
Systematics and Biology of Silica Bodies in Monocotyledons
inferredcites →https://doi.org/10.2307/1222979openalex-snapshot
Confidence limits in phylogenies: An example from the African Restionaceae
inferredcites →https://doi.org/10.2307/2666728openalex-snapshot
Congruence and Complementarity of Morphological and trnL-trnF Sequence Data and the Phylogeny of the African Restionaceae
inferredcites →https://doi.org/10.2307/2807789openalex-snapshot
Monocotyledons: Systematics and Evolution.
inferredcites →https://doi.org/10.2307/2996198openalex-snapshot
The Monocotyledons: A Comparative Study.
inferredcites →https://doi.org/10.2307/4108207openalex-snapshot
Anarthriaceae and Ecdeiocoleaceae: Two New Monocotyledonous Families, Separated from the Restionaceae
inferredcites →https://doi.org/10.2307/4110139openalex-snapshot
Pollen Morphology of Calorophus and Empodisma (Restionaceae) and Its Taxonomic Significance
inferredcites →https://doi.org/10.2307/4113660openalex-snapshot
Australian Rushes. Biology, Identification and Conservation of Restionaceae and Allied Families
inferredcites →https://doi.org/10.3417/2009142openalex-snapshot
Evolutionary History of the Monocot Flower 1
inferredcites →https://doi.org/10.3417/2010023openalex-snapshot
Assembling the Tree of the Monocotyledons: Plastome Sequence Phylogeny and Evolution of Poales 1
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.1100290openalex-snapshot
Homologies of the flower and inflorescence in the early‐divergent grass Anomochloa (Poaceae)
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.91.10.1645openalex-snapshot
Monocot relationships: an overview
inferredcites →https://doi.org/10.3897/phytokeys.13.3259openalex-snapshot
Systematics and ecology of the Australasian genus Empodisma (Restionaceae) and description of a new species from peatlands in northern New Zealand
inferredcites →https://doi.org/10.4102/abc.v40i1.178openalex-snapshot
A generic classification of the Restioneae (Restionaceae), southern Africa
inferredcites →https://doi.org/10.5281/zenodo.16031410openalex-snapshot
New combinations in Chordifex (Restionaceae) from eastern Australia and new species from Western Australia
inferredcites →https://doi.org/10.5642/aliso.20062201.06openalex-snapshot
Multigene Analyses of Monocot Relationships
inferredcites →https://doi.org/10.5642/aliso.20072301.16openalex-snapshot
Phylogeny and Historical Ecology of Rhodocoma (Restionaceae) from the Cape Floristic Region
inferredcites →https://doi.org/10.7751/telopea19982005openalex-snapshot
New genera and species of Australian Restionaceae (Poales)
inferredcites →https://doi.org/10.7751/telopea20002006openalex-snapshot
Hopkinsiaceae and Lyginiaceae, two new families of Poales in Western Australia, with revision of Hopkinsia and Lyginia
inferredcites →https://doi.org/10.7751/telopea20013002openalex-snapshot
New species of Harperia, Loxocarya, Onychosepalum, Platychorda and Tremulina (Restionaceae) in Western Australia
inferredcites →https://doi.org/10.7751/telopea20024023openalex-snapshot
Chromosome numbers of some native and naturalised plant species in 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)
inferredcites →https://doi.org/10.7751/telopea2012004openalex-snapshot
New species of Sporadanthus and Lepyrodia (Restionaceae) from eastern and western Australia
inferredcites →https://doi.org/10.7751/telopea2012005openalex-snapshot
New species and variation in Lepidobolus (Restionaceae) from Western Australia
inferredcites →https://doi.org/10.7751/telopea2012006openalex-snapshot
Chromosome numbers in some Australian Restionaceae (Poales): new counts and an inferred base number for Leptocarpoideae.
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.213.2.7zenodo-depositor-declared
Centrolepis milleri (Centrolepidaceae: Poales), a new species from Western Australia
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/ajb2.1178openalex-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/10.1007/s00606-024-01933-yopenalex-snapshot
Genome size variation and whole-genome duplications in the monocot order Poales
inferred← citeshttps://doi.org/10.1007/s11104-015-2764-2openalex-snapshot
Biodiversity hotspots and Ocbil theory
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/j.ppees.2018.08.001openalex-snapshot
Resolving the puzzle of Martin’s broad embryo: A solution based on morphology, taxonomy and phylogeny
inferred← citeshttps://doi.org/10.1071/bt14138openalex-snapshot
Synchronous monoecy in Ecdeiocoleaceae (Poales), in Western Australia
inferred← citeshttps://doi.org/10.1093/aesa/sav105openalex-snapshot
Restiid-Feeding Semiini (Hemiptera: Miridae: Phylinae) From Western Australia: Description and Phylogenetic Analysis of the New Plant Bug Genus Restiophylus , n. gen
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/botlinnean/boz011openalex-snapshot
Structure and development of female flowers in early-diverging restiids, Anarthria, Lyginia and Hopkinsia (Restionaceae s.l.): further evidence of multiple pathways of gynoecium reduction in wind-pollinated lineages of Poales
inferred← citeshttps://doi.org/10.1093/jxb/erac182openalex-snapshot
Evolutionary history of the grass gynoecium
inferred← citeshttps://doi.org/10.1111/boj.12233openalex-snapshot
Monocot fossils suitable for molecular dating analyses
inferred← citeshttps://doi.org/10.1111/boj.12283openalex-snapshot
The monocot fossil pollen record of New Zealand and its implications for palaeoclimates and environments
inferred← citeshttps://doi.org/10.1111/boj.12284openalex-snapshot
An update of monocot macrofossil data from New Zealand and Australia
inferred← citeshttps://doi.org/10.1111/boj.12285openalex-snapshot
Results from an online survey of family delimitation in angiosperms and ferns: recommendations to the Angiosperm Phylogeny Group for thorny problems in plant classification
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/nph.13331openalex-snapshot
On the complexity of triggering evolutionary radiations
inferred← citeshttps://doi.org/10.1111/nph.70667openalex-snapshot
Cryptic signals: substomatal architecture influences stomatal responses to red light and CO 2
inferred← citeshttps://doi.org/10.11648/j.plant.20251303.13openalex-snapshot
J. L. Reveal’s Revelance Re-revealed: Addenda to Newly Required Infrafamilial Ranks in Selected Families
inferred← citeshttps://doi.org/10.1186/1471-2148-14-102openalex-snapshot
Reconstructing the age and historical biogeography of the ancient flowering-plant family Hydatellaceae (Nymphaeales)
inferred← citeshttps://doi.org/10.12705/643.9openalex-snapshot
A genus‐level phylogenetic linear sequence of monocots
inferred← citeshttps://doi.org/10.12705/673.5openalex-snapshot
Nuclear genes, matK and the phylogeny of the Poales
inferred← citeshttps://doi.org/10.3103/s0096392517030105openalex-snapshot
Gynoecium evolution in angiosperms: Monomery, pseudomonomery, and mixomery
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/10.3390/d14090776openalex-snapshot
Plastomes Provide Insights into Differences between Morphology and Molecular Phylogeny: Ostericum and Angelica (Apiaceae) as an Example
inferred← citeshttps://doi.org/10.3390/plants15010097openalex-snapshot
Sexual Dimorphism on a Conserved Scaffold: Insights from the Floral Ontogeny of Eurychorda (Restionaceae: Poales)
inferred← citeshttps://doi.org/10.3732/ajb.1400434openalex-snapshot
Morphological diversity and evolution of Centrolepidaceae (Poales), a species‐poor clade with diverse body plans and developmental patterns
inferred← citeshttps://doi.org/10.7717/peerj.10935openalex-snapshot
Two centuries from species discovery to diagnostic characters: molecular and morphological evidence for narrower species limits in the widespread SW Australian Anarthria gracilis complex (Restionaceae s.l./Anarthriaceae, Poales)
inferred← citeshttps://doi.org/10.7751/telopea15543openalex-snapshot
Seeds and indehiscent fruit of Anarthriaceae and Australian Restionaceae: a gallery of micromorphology
inferred← citeshttps://doi.org/10.7751/telopea20147401openalex-snapshot
Apodasmia ceramophila, a new Western Australian species of Restionaceae
inferred← citeshttps://doi.org/10.7751/telopea20147402openalex-snapshot
Desmocladus (Restionaceae) enlarged to include the Western Australian Harperia, Kulinia and Onychosepalum
inferred← citeshttps://doi.org/10.7751/telopea8753openalex-snapshot
The identity of Restio trisepalus Nees, the new combination Leptocarpus trisepalus and lectotypifications in Australian Restionaceae
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