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Phylogenetic analysis ofIridaceae with parsimony and distance methods using the plastid generps4
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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.1994.1001openalex-snapshot
Anatomy and systematics of Iridaceae
inferredcites →https://doi.org/10.1006/mpev.1995.1024openalex-snapshot
A Phylogenetic Analysis of Monocotyledons Based on the Chloroplast Gene rps4, Using Parsimony and a New Numerical Phenetics Method
inferredcites →https://doi.org/10.1007/978-1-4020-6754-9_12413openalex-snapshot
PAUP (phylogenetic analysis using parsimony)
inferredcites →https://doi.org/10.1007/978-1-4615-3276-7_1openalex-snapshot
Chloroplast DNA and the Study of Plant Phylogeny: Present Status and Future Prospects
inferredcites →https://doi.org/10.1007/978-3-642-61663-1openalex-snapshot
The Families of the Monocotyledons
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/bf00161168openalex-snapshot
Rapid evolution of the plastid translational apparatus in a nonphotosynthetic plant: Loss or accelerated sequence evolution of tRNA and ribosomal protein genes
inferredcites →https://doi.org/10.1007/bf00351678openalex-snapshot
Molecular evolution of noncoding regions of the chloroplast genome in the Crassulaceae and related species
inferredcites →https://doi.org/10.1007/bf00418529openalex-snapshot
Conservation of chloroplast genome structure among vascular plants
inferredcites →https://doi.org/10.1007/bf00983551openalex-snapshot
Sedum surculosum andS. jaccardianum (Crassulaceae) share a unique 70 bp deletion in the chloroplast DNA trnL (UAA)-trnF (GAA) intergenic spacer
inferredcites →https://doi.org/10.1007/bf00985340openalex-snapshot
The chloroplast generps 4 as a tool for the study ofPoaceae phylogeny
inferredcites →https://doi.org/10.1007/bf00986193openalex-snapshot
Phylogeny ofRubiaceae-Rubieae inferred from the sequence of a cpDNA intergene region
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/s0254-6299(16)30815-8openalex-snapshot
Relationships of the southern African genus Bobartia (Iridaceae–Iridoideae)
inferredcites →https://doi.org/10.1016/s0959-437x(05)80202-3openalex-snapshot
Ins and outs of plastid genome evolution
inferredcites →https://doi.org/10.1073/pnas.79.16.5006openalex-snapshot
Chloroplast DNA evolution and phylogenetic relationships in Lycopersicon
inferredcites →https://doi.org/10.1073/pnas.91.15.6795openalex-snapshot
Rates and patterns of chloroplast DNA evolution.
inferredcites →https://doi.org/10.1086/284693openalex-snapshot
Evolutionary Analysis of Plant DNA Sequences
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/oxfordjournals.molbev.a040157openalex-snapshot
The use of chloroplast DNA to resolve plant phylogenies: noncoding versus rbcL sequences.
inferredcites →https://doi.org/10.1104/pp.63.4.660openalex-snapshot
Chloroplast DNA Sequence Homologies among Vascular Plants
inferredcites →https://doi.org/10.1111/j.1558-5646.1985.tb00420.xopenalex-snapshot
CONFIDENCE LIMITS ON PHYLOGENIES: AN APPROACH USING THE BOOTSTRAP
inferredcites →https://doi.org/10.1111/j.1558-5646.1988.tb02497.xopenalex-snapshot
THE LIMITS OF AMINO ACID SEQUENCE DATA IN ANGIOSPERM PHYLOGENETIC RECONSTRUCTION
inferredcites →https://doi.org/10.1111/j.1558-5646.1989.tb04260.xopenalex-snapshot
CHLOROPLAST‐DNA VARIATION AND MULTIPLE ORIGINS OF AUTOPOLYPLOIDY INHEUCHERA MICRANTHA(SAXIFRAGACEAE)
inferredcites →https://doi.org/10.1111/j.1558-5646.1990.tb05207.xopenalex-snapshot
EVOLUTIONARY SIGNIFICANCE OF THE LOSS OF THE CHLOROPLAST‐DNA INVERTED REPEAT IN THE LEGUMINOSAE SUBFAMILY PAPILIONOIDEAE
inferredcites →https://doi.org/10.1146/annurev.pp.38.060187.002135openalex-snapshot
Evolution of Higher-Plant Chloroplast DNA-Encoded Genes: Implications for Structure-Function and Phylogenetic Studies
inferredcites →https://doi.org/10.2307/1222465openalex-snapshot
An Integrated System of Classification of Flowering Plants
inferredcites →https://doi.org/10.2307/2399667openalex-snapshot
Phylogeny and Classification of Iridaceae
inferredcites →https://doi.org/10.2307/2399833openalex-snapshot
Pollination Biology of Lapeirousia Subgenus Lapeirousia (Iridaceae) in Southern Africa; Floral Divergence and Adaptation for Long-Tongued Fly Pollination
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/10.2307/2399875openalex-snapshot
Phylogenetic Inference in Saxifragaceae Sensu Stricto and Gilia (Polemoniaceae) Using matK Sequences
inferredcites →https://doi.org/10.2307/2399876openalex-snapshot
Evidence for the Polyphyly of the Scrophulariaceae Based on Chloroplast rbcL and ndhF Sequences
inferredcites →https://doi.org/10.2307/2399877openalex-snapshot
The Utility of atpB Gene Sequences in Resolving Phylogenetic Relationships: Comparison with rbcL and 18S Ribosomal DNA Sequences in the Lardizabalaceae
inferredcites →https://doi.org/10.2307/2419717openalex-snapshot
Phylogenetic Analyses of Polemoniaceae Using Nucleotide Sequences of the Plastid Gene matK
inferredcites →https://doi.org/10.2307/2419718openalex-snapshot
matK DNA Sequences and Phylogenetic Reconstruction in Saxifragaceae s. str.
inferredcites →https://doi.org/10.2307/2806386openalex-snapshot
An Integrated System of Classification of Flowering Plants.
inferredcites →https://doi.org/10.2307/2807789openalex-snapshot
Monocotyledons: Systematics and Evolution.
inferredcites →https://doi.org/10.5860/choice.39-2183openalex-snapshot
MacClade 4.0: analysis of phylogeny and character evolution
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Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Chloroplast phylogenies of Australasian Gleichenia ferns (Gleicheniaceae) reveal incongruence with current taxonomy, and frequent long-distance dispersal
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inferred← citeshttps://doi.org/10.1007/s12041-017-0755-1openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s12228-016-9437-1openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.palwor.2007.07.003openalex-snapshot
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inferred← citeshttps://doi.org/10.1093/botlinnean/boag011openalex-snapshot
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inferred← citeshttps://doi.org/10.1093/botlinnean/boag048openalex-snapshot
Cenozoic diversification in a Pan-Himalayan context: the case of Chinese ferns Hymenophyllum subg. Mecodium (Hymenophyllaceae)
inferred← citeshttps://doi.org/10.1094/cchem.1999.76.3.371openalex-snapshot
Fate of Maize DNA During Steeping, Wet‐Milling, and Processing
inferred← citeshttps://doi.org/10.1111/boj.12360openalex-snapshot
Is it really you, Orthotrichum acuminatum ? Ascertaining a new case of intercontinental disjunction in mosses
inferred← citeshttps://doi.org/10.1111/cla.12094openalex-snapshot
A global plastid phylogeny of the brake fern genus Pteris (Pteridaceae) and related genera in the Pteridoideae
inferred← citeshttps://doi.org/10.1111/cla.12384openalex-snapshot
A global plastid phylogeny of the fern genus Asplenium (Aspleniaceae)
inferred← citeshttps://doi.org/10.1111/cla.12408openalex-snapshot
Evolutionary relationships of the ancient fern lineage the adder's tongues (Ophioglossaceae) with description of Sahashia gen. nov
inferred← citeshttps://doi.org/10.1111/cla.12539openalex-snapshot
Splitting one species into 22: an unusual tripling of molecular, morphological, and geographical differentiation in the fern family Didymochlaenaceae (Polypodiales)
inferred← citeshttps://doi.org/10.1111/j.0024-4074.2004.00246.xopenalex-snapshot
Phylogeny of the Afro-Madagascan Aristea (Iridaceae) revisited in the light of new data on pollen morphology
inferred← citeshttps://doi.org/10.1111/j.1095-8339.2007.00743.xopenalex-snapshot
Origin and relationships of the myco-heterotrophic liverwort Cryptothallus mirabilis Malmb. (Metzgeriales, Marchantiophyta)
inferred← citeshttps://doi.org/10.1111/j.1469-8137.2010.03351.xopenalex-snapshot
Diversification and biogeography of Juniperus (Cupressaceae): variable diversification rates and multiple intercontinental dispersals
inferred← citeshttps://doi.org/10.1111/j.1469-8137.2011.03783.xopenalex-snapshot
Evolution of sexual systems, dispersal strategies and habitat selection in the liverwort genus Radula
inferred← citeshttps://doi.org/10.1111/j.1601-5223.2004.01839.xopenalex-snapshot
The genomic organization and evolutionary distribution of a tandemly repeated DNA sequence family in the genus Crocus (Iridaceae)
inferred← citeshttps://doi.org/10.1111/j.1759-6831.2009.00063.xopenalex-snapshot
Evaluation of 10 plant barcodes in Bryophyta (Mosses)
inferred← citeshttps://doi.org/10.1111/jse.12305openalex-snapshot
Pteridryaceae: A new fern family of Polypodiineae (Polypodiales) including taxonomic treatments
inferred← citeshttps://doi.org/10.1111/jse.13194openalex-snapshot
Phylogeny and biogeography of the fern genus Hymenasplenium (Aspleniaceae), with special reference to island speciation
inferred← citeshttps://doi.org/10.1111/jse.70088openalex-snapshot
Molecular phylogenetic analysis sheds light on the diversity and evolutionary history of the Neotropical and African Triplophyllum (Tectariaceae)
inferred← citeshttps://doi.org/10.11110/kjpt.2019.49.2.127openalex-snapshot
Exploring natural hybridizations among Asplenium ruprechtii and related taxa in Korea
inferred← citeshttps://doi.org/10.11110/kjpt.2020.50.4.403openalex-snapshot
Identification of three independent fern gametophytes and Hymenophyllum wrightii f. serratum from Korea based on molecular data
inferred← citeshttps://doi.org/10.11110/kjpt.2024.54.4.267openalex-snapshot
Reticulate evolution in the Asplenium anogrammoides complex from Korea
inferred← citeshttps://doi.org/10.1134/s0012496609030144openalex-snapshot
The species status of Iris vorobievii N.S. Pavlova, I. mandshurica Maxim., and I. humilis Georgi (Iridaceae): Evidence from the plastid genome
inferred← citeshttps://doi.org/10.1134/s1022795409110143openalex-snapshot
Independent species status of Iris vorobievii N.S. Pavlova, Iris mandshurica Maxim., and Iris humilis Georgi (Iridaceae): Evidence from the nuclear and chloroplast genomes
inferred← citeshttps://doi.org/10.11646/phytotaxa.9.1.11openalex-snapshot
20,000 species and five key markers: The status of molecular bryophyte phylogenetics
inferred← citeshttps://doi.org/10.1179/1743282011y.0000000015openalex-snapshot
The status ofStruckiaMüll.Hal. (Plagiotheciaceae, Bryopsida) inferred from multiple nuclear and chloroplast loci
inferred← citeshttps://doi.org/10.1179/1743282011y.0000000035openalex-snapshot
Differences in spatial genetic structure and diversity in two mosses with different dispersal strategies in a fragmented landscape
inferred← citeshttps://doi.org/10.1179/1743282013y.0000000072openalex-snapshot
The identity ofRadula carringtoniiJack
inferred← citeshttps://doi.org/10.1186/1471-2148-12-180openalex-snapshot
Molecular circumscription and major evolutionary lineages of the fern genus Dryopteris (Dryopteridaceae)
inferred← citeshttps://doi.org/10.1186/s12862-016-0626-zopenalex-snapshot
Using a multilocus phylogeny to test morphology-based classifications of Polystichum (Dryopteridaceae), one of the largest fern genera
inferred← citeshttps://doi.org/10.1186/s12870-014-0361-9openalex-snapshot
Identification of the relationship between Chinese Adiantum reniforme var. sinense and Canary Adiantum reniforme
inferred← citeshttps://doi.org/10.12705/626.13openalex-snapshot
The fern genus Adenoderris (family incertae sedis) is artificial
inferred← citeshttps://doi.org/10.12705/626.15openalex-snapshot
Unnoticed diversity within the disjunct moss Orthotrichum tenellum s.l. validated by morphological and molecular approaches
inferred← citeshttps://doi.org/10.12705/641.4openalex-snapshot
Didymochlaenaceae: A new fern family of eupolypods I (Polypodiales)
inferred← citeshttps://doi.org/10.12705/646.3openalex-snapshot
Molecular phylogeny and character evolution of Anemiaceae (Schizaeales)
inferred← citeshttps://doi.org/10.12705/654.3openalex-snapshot
Circumscription and phylogeny of the fern family Tectariaceae based on plastid and nuclear markers, with the description of two new genera: Draconopteris and Malaifilix (Tectariaceae)
inferred← citeshttps://doi.org/10.1371/journal.pone.0018212openalex-snapshot
Does Variation in Genome Sizes Reflect Adaptive or Neutral Processes? New Clues from Passiflora
inferred← citeshttps://doi.org/10.1371/journal.pone.0112510openalex-snapshot
Novel Biogenic Aggregation of Moss Gemmae on a Disappearing African Glacier
inferred← citeshttps://doi.org/10.1371/journal.pone.0172729openalex-snapshot
Revision of series Gravesiana (Adiantum L.) based on morphological characteristics, spores and phylogenetic analyses
inferred← citeshttps://doi.org/10.1371/journal.pone.0211017openalex-snapshot
The long journey of Orthotrichum shevockii (Orthotrichaceae, Bryopsida): From California to Macaronesia
inferred← citeshttps://doi.org/10.1371/journal.pone.0358245openalex-snapshot
Molecular identification and diversity assessment of Tyrrhenian Romulea species (Iridaceae)
inferred← citeshttps://doi.org/10.15298/arctoa.30.03openalex-snapshot
A further range extension of Redfearnia (Bryophyta, Amblystegiaceae), with new data on its phylogenic position
inferred← citeshttps://doi.org/10.15298/arctoa.35.02openalex-snapshot
New species of liverwort from Yakutia (Russian Arctic): when striking morphological differences are not supported from DNA
inferred← citeshttps://doi.org/10.1590/s1415-47572012000600018openalex-snapshot
Studies on diversity and evolution of Iridaceae species in southern Brazil
inferred← citeshttps://doi.org/10.1590/s1415-47572012000600019openalex-snapshot
Phylogeny, biogeography and divergence times in Passiflora (Passifloraceae)
inferred← citeshttps://doi.org/10.1600/036364406775971697openalex-snapshot
Rank-Free Monography: A Practical Example From the Moss Clade Leucophanella (Calymperaceae)
inferred← citeshttps://doi.org/10.1600/036364408785679806openalex-snapshot
Iridaceae 'Out of Australasia'? Phylogeny, Biogeography, and Divergence Time Based on Plastid DNA Sequences
inferred← citeshttps://doi.org/10.1600/036364412x616666openalex-snapshot
Phylogeny of the New World Genus Sisyrinchium (Iridaceae) Based on Analyses of Plastid and Nuclear DNA Sequence Data
inferred← citeshttps://doi.org/10.1600/036364414x680933openalex-snapshot
The Phylogenetic Relationship of Tectaria brauniana and Tectaria nicotianifolia, and the Recognition of Hypoderris (Tectariaceae)
inferred← citeshttps://doi.org/10.1600/036364416x690660openalex-snapshot
Maidenhair Ferns, Adiantum, are Indeed Monophyletic and Sister to Shoestring Ferns, Vittarioids (Pteridaceae)
inferred← citeshttps://doi.org/10.1600/036364417x694557openalex-snapshot
Two Beringian Origins for the Allotetraploid Fern Polystichum braunii (Dryopteridaceae)
inferred← citeshttps://doi.org/10.1600/036364417x695952openalex-snapshot
Taxonomic Placement of Unassigned Species of Lastreopsid Ferns (Dryopteridaceae) Using Phylogeny
inferred← citeshttps://doi.org/10.1600/036364420x16033962925150openalex-snapshot
Revision of Hymenophyllum subg. Sphaerocionium (Hymenophyllaceae) in the Atlantic Forest Domain (Brazil), Based on Molecular and Morphological Evidence
inferred← citeshttps://doi.org/10.1600/036364421x16231782047451openalex-snapshot
A Reassessment of the Little-Known Amazonian Fern Diplazium praestans Based on Molecular and Morphological Evidence
inferred← citeshttps://doi.org/10.1600/036364421x16312067913507openalex-snapshot
Studies of Vietnamese Pteridophyte Flora 1
inferred← citeshttps://doi.org/10.1600/036364421x16370109698605openalex-snapshot
Phylogeny and Character Evolution of the Neotropical Fern Genus Cyclodium (Dryopteridaceae)
inferred← citeshttps://doi.org/10.1600/036364423x16847773873062openalex-snapshot
Hymenophyllum subg. Hymenophyllum (Hymenophyllaceae) in the Atlantic Forest Domain, Brazil: Phylogenetic Relationships and Taxonomic Review
inferred← citeshttps://doi.org/10.1600/036364423x16847773873161openalex-snapshot
Studies of Vietnamese Pteridophyte Flora 2
inferred← citeshttps://doi.org/10.1639/0007-2745(2000)103[0257:prwthm]2.0.co;2openalex-snapshot
Phylogenetic Relationships Within the Haplolepideous Mosses
inferred← citeshttps://doi.org/10.1639/0007-2745(2006)109[224:psoggb]2.0.co;2openalex-snapshot
Phylogenetic study ofGrimmia(Grimmiaceae) based on plastid DNA sequences (trnL-trnF andrps4) and on morphological characters
inferred← citeshttps://doi.org/10.1639/0007-2745(2007)110[46:potcwa]2.0.co;2openalex-snapshot
Phylogeny of the Calymperaceae with a rank-free systematic treatment
inferred← citeshttps://doi.org/10.1639/0007-2745-112.1.80openalex-snapshot
Phylogenetic relationships of the Thuidiaceae and the non-monophyly of the Thuidiaceae and the Leskeaceae based onrbcL,rps4 and therps4-trnS intergenic spacer
inferred← citeshttps://doi.org/10.1639/0007-2745-112.3.447openalex-snapshot
Phylogenetic analyses reveal high levels of polyphyly among pleurocarpous lineages as well as novel clades
inferred← citeshttps://doi.org/10.1639/0007-2745-114.3.547openalex-snapshot
Phylogenetic relationships of Yunnanobryon (Musci: Regmatodontaceae)
inferred← citeshttps://doi.org/10.1639/0007-2745-122.4.559openalex-snapshot
Reappraisal of Taxiphyllum arcuatum (Bosch & Sande Lac.) S.He based on molecular and morphological data
inferred← citeshttps://doi.org/10.1639/0007-2745-123.4.601openalex-snapshot
Morphology of gemmae, an overlooked taxonomic trait in the genus Marchantia L. (Marchantiaceae)
inferred← citeshttps://doi.org/10.1639/0007-2745-124.3.403openalex-snapshot
So close yet so far: the disjunct global range of Orthotrichum consobrinum (Orthotrichaceae) includes North America
inferred← citeshttps://doi.org/10.1639/0007-2745-125.2.343openalex-snapshot
Encalypta sylvatica, a new species of Encalyptaceae from northern China
inferred← citeshttps://doi.org/10.1639/0007-2745-127.1.095openalex-snapshot
Systematic Position of Calypogeia asakawana S.Hatt. ex Inoue (Calypogeiaceae, Marchantiophyta), with Description of a New Genus Protocalypogeia
inferred← citeshttps://doi.org/10.1640/0002-8444(2004)094[0126:protst]2.0.co;2openalex-snapshot
Phylogenetic Relationships of the Subfamily Taenitidoideae, Pteridaceae
inferred← citeshttps://doi.org/10.1640/0002-8444-101.3.142openalex-snapshot
Phylogenetic Positions of the Enigmatic Asiatic Fern Genera Diplaziopsis and Rhachidosorus from Analyses of Four Plastid Genes
inferred← citeshttps://doi.org/10.1640/0002-8444-103.2.118openalex-snapshot
Polystichum montevidenseDemystified: Molecular and Morphological Data Reveal a Cohesive, Widespread South American Species
inferred← citeshttps://doi.org/10.1640/0002-8444-110.4.151openalex-snapshot
Speciation and Reticulation in the Polystichum Allotetraploids of the Costa Rican Cordillera Talamanca
inferred← citeshttps://doi.org/10.1640/0002-8444-111.1.24openalex-snapshot
The Platycerium Variant from Mount Lewis, Australia
inferred← citeshttps://doi.org/10.18475/cjos.v51i2.a13openalex-snapshot
DNA Barcoding of Adiantum (Pteridaceae: Vittarioideae) in Puerto Rico
inferred← citeshttps://doi.org/10.18968/hattoria.9.0_41openalex-snapshot
Phylogenetic position of the East Asian endemic genus Hattoria (Anastrophyllaceae) based on chloroplast DNA sequences
inferred← citeshttps://doi.org/10.2307/25065733openalex-snapshot
Evolution of leafy liverworts (Jungermanniidae, Marchantiophyta): estimating divergence times from chloroplast DNA sequences using penalized likelihood with integrated fossil evidence
inferred← citeshttps://doi.org/10.2307/3391858openalex-snapshot
Reduction of Barnardiella, Galaxia, Gynandriris, Hexaglottis, Homeria, and Roggeveldia in Moraea (Iridaceae: Irideae)
inferred← citeshttps://doi.org/10.2307/3558433openalex-snapshot
Molecular systematics of Iridaceae: evidence from four plastid DNA regions
inferred← citeshttps://doi.org/10.2478/s11756-010-0008-8openalex-snapshot
Historical herbarium specimens in plant molecular systematics — an example from the fern genus Lindsaea (Lindsaeaceae)
inferred← citeshttps://doi.org/10.31111/nsnr/2026.60.2.b1openalex-snapshot
Contribution to the bryoflora of Svalbard (Norway): new finds of species and deviating forms of mosses regarding from integrative study
inferred← citeshttps://doi.org/10.3389/fevo.2018.00108openalex-snapshot
Phylogeny and Biogeography of Carnivorous Plant Family Nepenthaceae With Reference to the Indian Pitcher Plant Nepenthes Khasiana Reveals an Indian Subcontinent Origin of Nepenthes Colonization in South East Asia During the Miocene Epoch
inferred← citeshttps://doi.org/10.3389/fpls.2020.502359openalex-snapshot
Latitudinal Biogeographic Structuring in the Globally Distributed Moss Ceratodon purpureus
inferred← citeshttps://doi.org/10.3389/fpls.2021.629035openalex-snapshot
Insights Into the Evolutionary History of the Subfamily Orthotrichoideae (Orthotrichaceae, Bryophyta): New and Former Supra-Specific Taxa So Far Obscured by Prevailing Homoplasy
inferred← citeshttps://doi.org/10.3389/fpls.2023.1066708openalex-snapshot
A phylogenomic study of Iridaceae Juss. based on complete plastid genome sequences
inferred← citeshttps://doi.org/10.3390/plants11243557openalex-snapshot
Codonoblepharonteae, a New Major Lineage among Orthotrichoideae (Orthotrichaceae, Bryophyta)
inferred← citeshttps://doi.org/10.3390/taxonomy1030019openalex-snapshot
Finding Hidden Outliers to Promote the Consistency of Key Morphological Traits and Phylogeny in Dennstaedtiaceae
inferred← citeshttps://doi.org/10.3417/2019371openalex-snapshot
The Decursivum Group of Elaphoglossum sect. Polytrichia (Dryopteridaceae): Non-subulate Species Nested in an Otherwise Subulate-scaled Clade
inferred← citeshttps://doi.org/10.3724/sp.j.1003.2011.08239openalex-snapshot
The rps4 locus as an alternative marker for barcoding bryo-phytes: eva-luation based on data mining from GenBank
inferred← citeshttps://doi.org/10.3732/ajb.0900019openalex-snapshot
Deciphering the origins of apomictic polyploids in the Cheilanthes yavapensis complex (Pteridaceae)
inferred← citeshttps://doi.org/10.3732/ajb.0900393openalex-snapshot
Molecular phylogeny, character evolution, and biogeography of the grammitid fern genus Lellingeria (Polypodiaceae)
inferred← citeshttps://doi.org/10.3732/ajb.1100125openalex-snapshot
Biogeographic disjunction between eastern Asia and North America in the Adiantum pedatum complex (Pteridaceae)
inferred← citeshttps://doi.org/10.3732/ajb.1300191openalex-snapshot
Phylogeny and biogeography of exindusiate Andean Polystichum (Dryopteridaceae)
inferred← citeshttps://doi.org/10.3732/ajb.1300269openalex-snapshot
A comparison of 16 DNA regions for use as phylogenetic markers in the pleurocarpous moss genus Plagiothecium (Hypnales)
inferred← citeshttps://doi.org/10.3732/ajb.1400071openalex-snapshot
Phylogeny and historical biogeography of the lastreopsid ferns (Dryopteridaceae)
inferred← citeshttps://doi.org/10.3732/ajb.90.12.1777openalex-snapshot
Polarity of peatmoss ( Sphagnum ) evolution: who says bryophytes have no roots?
inferred← citeshttps://doi.org/10.3732/ajb.90.8.1229openalex-snapshot
A first molecular phylogenetic analysis of Passiflora (Passifloraceae)
inferred← citeshttps://doi.org/10.3732/ajb.91.2.274openalex-snapshot
Phylogenetics and biogeography of the neotropical fern genera Jamesonia and Eriosorus (Pteridaceae)
inferred← citeshttps://doi.org/10.3897/phytokeys.14.3446openalex-snapshot
Phylogenetic analyses place the Australian monotypic Revwattsia in Dryopteris (Dryopteridaceae)
inferred← citeshttps://doi.org/10.3897/phytokeys.186.73739openalex-snapshot
Dipteris shenzhenensis, a new endangered species of Dipteridaceae from Shenzhen, southern China
inferred← citeshttps://doi.org/10.3897/phytokeys.187.77035openalex-snapshot
Two new species in the fern genus Lomariopsis (Lomariopsidaceae) from East Asia
inferred← citeshttps://doi.org/10.3897/phytokeys.204.86045openalex-snapshot
Hymenophyllum chamaecyparicola (Hymenophyllaceae), a new filmy fern species from Taiwan
inferred← citeshttps://doi.org/10.3897/phytokeys.35.6886openalex-snapshot
Tryonia, a new taenitidoid fern genus segregated from Jamesonia and Eriosorus (Pteridaceae)
inferred← citeshttps://doi.org/10.4462/annbotrm-9059openalex-snapshot
PHYLOGENY AND CLASSIFICATION OF THE IRIDACEAE AND THE RELATIONSHIPS OF IRIS
inferred← citeshttps://doi.org/10.4462/annbotrm-9060openalex-snapshot
MOLECULAR SYSTEMATICS OF IRIDACEAE: A COMBINED ANALYSIS OF FOUR PLASTID DNA SEQUENCE MATRICES
inferred← citeshttps://doi.org/10.4462/annbotrm-9063openalex-snapshot
FLORAL ANATOMY AND SYSTEMATIC POSITION OF DIPLARRHENA (IRIDACEAE): A NEW TRIBE DIPLARRHENEAE
inferred← citeshttps://doi.org/10.48550/arxiv.1902.06032openalex-snapshot
Molecular Phylogeny of Chinese Thuidiaceae with emphasis on Thuidium and Pelekium
inferred← citeshttps://doi.org/10.54207/bsmps1000-2004-4hx573openalex-snapshot
Geographical distribution of Iridaceae in India
inferred← citeshttps://doi.org/10.5504/bbeq.2011.0075openalex-snapshot
Genetic Diversity and Molecular Taxonomy Study of Three Genera fromIridaceaeFamily in the Bulgarian Flora Based on ISSR Markers
inferred← citeshttps://doi.org/10.7717/peerj.9109openalex-snapshot
At the crossroads of botanical collections and molecular genetics laboratory: a preliminary study of obtaining amplifiable DNA from moss herbarium material
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