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Molecular Markers Reject Monophyly of the Subgenera of Satyrium (Orchidaceae)

https://doi.org/10.1600/0363644054223530
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What this work says

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

inferredcites →https://doi.org/10.1006/bojl.1995.0013openalex-snapshot
Comparative vegetative anatomy and classification of Diseae (Orchidaceae)
inferredcites →https://doi.org/10.1006/clad.1996.0016openalex-snapshot
ON SIMULTANEOUS ANALYSIS
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/bf00985575openalex-snapshot
Do pollinators determine hybridization patterns in sympatricSatyrium (Orchidaceae) species?
inferredcites →https://doi.org/10.1007/s00606-004-0133-3openalex-snapshot
A phylogenetic analysis of Apostasioideae (Orchidaceae) based on ITS, trnL-F and matK sequences
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/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/s0367-2530(17)30686-2openalex-snapshot
Floral morphology and ontogeny in subtribe Satyriinae (Fam. Orchidaceae)
inferredcites →https://doi.org/10.1016/s1055-7903(02)00235-xopenalex-snapshot
Radiation in the Cape flora and the phylogeny of peacock irises Moraea (Iridaceae) based on four plastid DNA regions
inferredcites →https://doi.org/10.1080/10635150116801openalex-snapshot
Failure of the ILD to Determine Data Combinability for Slow Loris Phylogeny
inferredcites →https://doi.org/10.1093/bioinformatics/13.3.235openalex-snapshot
Seq-Gen: an application for the Monte Carlo simulation of DNA sequence evolution along phylogenetic trees
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/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/sysbio/38.1.7openalex-snapshot
A Concern for Evidence and a Phylogenetic Hypothesis of Relationships among Epicrates (Boidae, Serpentes)
inferredcites →https://doi.org/10.1093/sysbio/42.3.368openalex-snapshot
For Consensus (Sometimes)
inferredcites →https://doi.org/10.1093/sysbio/42.3.384openalex-snapshot
Partitioning and Combining Data in Phylogenetic Analysis
inferredcites →https://doi.org/10.1093/sysbio/44.1.3openalex-snapshot
Approaches for Assessing Phylogenetic Accuracy
inferredcites →https://doi.org/10.1093/sysbio/44.1.64openalex-snapshot
Testing Species Phylogenies and Phylogenetic Methods with Congruence
inferredcites →https://doi.org/10.1093/sysbio/45.4.546openalex-snapshot
A Likelihood-Ratio Test of Monophyly
inferredcites →https://doi.org/10.1093/sysbio/49.2.369openalex-snapshot
Gaps as Characters in Sequence-Based Phylogenetic Analyses
inferredcites →https://doi.org/10.1111/j.1095-8339.1889.tb00795.xopenalex-snapshot
Contributions to South-African Botany.- Part IV. (With a Revised List of published Species of Extra-tropical South-African Orchids).
inferredcites →https://doi.org/10.1111/j.1096-0031.1994.tb00181.xopenalex-snapshot
TESTING SIGNIFICANCE OF INCONGRUENCE
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.es.26.110195.003301openalex-snapshot
SEPARATE VERSUS COMBINED ANALYSIS OF PHYLOGENETIC EVIDENCE
inferredcites →https://doi.org/10.2307/2398858openalex-snapshot
An Analysis of the Flora of Southern Africa: Its Characteristics, Relationships, and Orgins
inferredcites →https://doi.org/10.2307/2399916openalex-snapshot
The Phylogeny and Classification of the Diseae (Orchidoideae: Orchidaceae)
inferredcites →https://doi.org/10.2307/2656709openalex-snapshot
Molecular phylogenetics of Diseae (Orchidaceae): a contribution from nuclear ribosomal ITS sequences
inferredcites →https://doi.org/10.2307/2656837openalex-snapshot
Subtribal and generic relationships of Maxillarieae (Orchidaceae) with emphasis on Stanhopeinae: combined molecular evidence
inferredcites →https://doi.org/10.2307/2657022openalex-snapshot
Phylogenetic relationships of Loasaceae subfamily Gronovioideae inferred from matK and ITS sequence data
inferredcites →https://doi.org/10.2307/2657116openalex-snapshot
The dalbergioid legumes (Fabaceae): delimitation of a pantropical monophyletic clade
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/10.2307/3558367openalex-snapshot
Molecular phylogeny of Coelogyne (Epidendroideae; Orchidaceae) based on plastid RFLPS, matK, and nuclear ribosomal ITS sequences: evidence for polyphyly
inferredcites →https://doi.org/10.2307/3558390openalex-snapshot
Phylogenetic relationships in Pleurothallidinae (Orchidaceae): combined evidence from nuclear and plastid DNA sequences
inferredcites →https://doi.org/10.2307/3558433openalex-snapshot
Molecular systematics of Iridaceae: evidence from four plastid DNA regions
inferredcites →https://doi.org/10.2307/3558434openalex-snapshot
Phylogenetic relationships in Disa based on non‐coding trnL‐trnF chloroplast sequences: evidence of numerous repeat regions
inferredcites →https://doi.org/10.3732/ajb.90.3.481openalex-snapshot
Phylogenetic analysis of Asplenium subgenus Ceterach (Pteridophyta: Aspleniaceae) based on plastid and nuclear ribosomal ITS DNA sequences
inferredcites →https://doi.org/10.3732/ajb.90.5.777openalex-snapshot
Phylogenetics of Cranichideae with emphasis on Spiranthinae (Orchidaceae, Orchidoideae): evidence from plastid and nuclear DNA sequences
inferredcites →https://doi.org/10.5860/choice.31-2679openalex-snapshot
Phylogeny and classification of the orchid family

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.696.3.4zenodo-depositor-declared
Chromosome numbers and molecular phylogenetics of some endemic orchid species (Orchidaceae) of Sri Lanka
inferred← citeshttps://doi.org/10.1002/tax.594006openalex-snapshot
Contribution of mitochondrial cox1 intron sequences to the phylogenetics of tribe Orchideae (Orchidaceae): Do the distribution and sequence of this intron in orchids also tell us something about its evolution?
inferred← citeshttps://doi.org/10.1007/978-981-99-4853-6_6openalex-snapshot
Plants of Tribe Orchideae
inferred← citeshttps://doi.org/10.1007/s00606-010-0411-1openalex-snapshot
Diverse pollination systems of the twin-spurred orchid genus Satyrium in African grasslands
inferred← citeshttps://doi.org/10.1007/s00606-016-1378-3openalex-snapshot
Ancient divergence and contrasting floral biology of the two species of Pachites (Orchidaceae)
inferred← citeshttps://doi.org/10.1007/s10531-017-1343-7openalex-snapshot
High-throughput sequencing of African chikanda cake highlights conservation challenges in orchids
inferred← citeshttps://doi.org/10.1016/j.cub.2020.10.024openalex-snapshot
Food Reward Chemistry Explains a Novel Pollinator Shift and Vestigialization of Long Floral Spurs in an Orchid
inferred← citeshttps://doi.org/10.1016/j.flora.2026.152967openalex-snapshot
Multiple lines of evidence confirm predicted moth pollination of the fragrant, foliage-coloured Cape orchid Satyrium odorum
inferred← citeshttps://doi.org/10.1016/j.sajb.2008.01.002openalex-snapshot
The phylogenetic position of the enigmatic orchid genus Pachites
inferred← citeshttps://doi.org/10.1016/j.sajb.2008.06.006openalex-snapshot
Satyrium situsanguinum (Orchidaceae): A new species from the Western Cape, South Africa
inferred← citeshttps://doi.org/10.1016/j.sajb.2010.08.010openalex-snapshot
Disa albomagentea (Orchidaceae), a new species from the Hottentots Holland Mountains in the Cape Floristic Region, South Africa
inferred← citeshttps://doi.org/10.1016/j.sajb.2017.03.018openalex-snapshot
Satyrium liltvedianum: A newly discovered orchid species from the Kogelberg Mountains of the Cape Floristic Region (South Africa)
inferred← citeshttps://doi.org/10.1016/j.sajb.2018.05.023openalex-snapshot
Autonomous self-pollination in the South African orchid Satyrium rupestre Schltr.
inferred← citeshttps://doi.org/10.1016/j.ympev.2006.08.014openalex-snapshot
A molecular phylogeny for the large African orchid genus Disa
inferred← citeshttps://doi.org/10.1016/j.ympev.2007.12.008openalex-snapshot
Dealing with incongruence in the quest for the species tree: A case study from the orchid genus Satyrium
inferred← citeshttps://doi.org/10.1016/j.ympev.2008.05.020openalex-snapshot
Pollinators underestimated: A molecular phylogeny reveals widespread floral convergence in oil-secreting orchids (sub-tribe Coryciinae) of the Cape of South Africa
inferred← citeshttps://doi.org/10.1016/j.ympev.2008.09.004openalex-snapshot
Phylogenetic relationships of Ruteae (Rutaceae): New evidence from the chloroplast genome and comparisons with non-molecular data
inferred← citeshttps://doi.org/10.1093/aob/mcaf074openalex-snapshot
Geographical variation in flower colour of a food-deceptive orchid reflects local pollinator preferences
inferred← citeshttps://doi.org/10.1093/aob/mcr048openalex-snapshot
Carrion mimicry in a South African orchid: flowers attract a narrow subset of the fly assemblage on animal carcasses
inferred← citeshttps://doi.org/10.1093/botlinnean/boaa018openalex-snapshot
A morphometric and molecular phylogenetic analysis of the African orchid genusStenoglottis(Orchidaceae: Orchidoideae)
inferred← citeshttps://doi.org/10.1093/botlinnean/boaa041openalex-snapshot
Is biodiversity underestimated by classical herbarium-based taxonomy? A multi-disciplinary case study inSatyrium(Orchidaceae)
inferred← citeshttps://doi.org/10.1093/botlinnean/boac078openalex-snapshot
Widespread coexistence of genetically distinct morphotypes in theSatyrium longicaudacomplex (Orchidaceae)
inferred← citeshttps://doi.org/10.1111/boj.12136openalex-snapshot
Phylogenetic position and floral morphology of the Brazilian endemic, monospecific genusCotylolabium: a sister group for the remaining Spiranthinae (Orchidaceae)
inferred← citeshttps://doi.org/10.1111/j.1095-8339.2011.01143.xopenalex-snapshot
More than meets the eye: a morphological and phylogenetic comparison of long-spurred, white-flowered Satyrium species (Orchidaceae) in South Africa
inferred← citeshttps://doi.org/10.1111/j.1095-8339.2011.01161.xopenalex-snapshot
Molecular phylogenetics, floral convergence and systematics of Dichromanthus and Stenorrhynchos (Orchidaceae: Spiranthinae)
inferred← citeshttps://doi.org/10.1111/j.1467-8748.2011.01742.xopenalex-snapshot
710. SATYRIUM PRINCEPS
inferred← citeshttps://doi.org/10.1111/j.1529-8817.2006.00175.xopenalex-snapshot
PROPOSAL OF THE EUPTILOTEAE HOMMERSAND ET FREDERICQ, TRIB. NOV. AND TRANSFER OF SOME SOUTHERN HEMISPHERE PTILOTEAE TO THE CALLITHAMNIEAE (CERAMIACEAE, RHODOPHYTA)1
inferred← citeshttps://doi.org/10.1111/plb.12196openalex-snapshot
Is the timing of scent emission correlated with insect visitor activity and pollination in long‐spurred Satyrium species?
inferred← citeshttps://doi.org/10.1186/s12870-017-1160-xopenalex-snapshot
Phylogenetics of subtribe Orchidinae s.l. (Orchidaceae; Orchidoideae) based on seven markers (plastid matK, psaB, rbcL, trnL-F, trnH-psba, and nuclear nrITS, Xdh): implications for generic delimitation
inferred← citeshttps://doi.org/10.2478/biorc-2021-0004openalex-snapshot
Contribution to the taxonomic revision ofBrachycorythis-complex (Orchidaceae, Orchidoideae)
inferred← citeshttps://doi.org/10.3897/subtbiol.10.4154openalex-snapshot
Molecular divergence and evolutionary relationships among Aemodogryllinae from Southern China, Laos and Thailand (Orthoptera, Rhaphidophoridae)
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