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Phylogenetic Hypotheses for the Monocotyledons Constructed from rbcL Sequence Data

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inferredcites →https://doi.org/10.1007/978-3-642-61663-1openalex-snapshot
The Families of the Monocotyledons
inferredcites →https://doi.org/10.1007/bf01734359openalex-snapshot
Evolutionary trees from DNA sequences: A maximum likelihood approach

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Premeiotic Microsporocyte Cell Shape Influences Shape of Tetrads during Microsporogenesis
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Five vicarious genera from Gondwana: the Velloziaceae as shown by molecules and morphology
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Five vicariant genera from Gondwana: the Velloziaceae as shown by molecules and morphology
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Using Phylogenomic Patterns and Gene Ontology to Identify Proteins of Importance in Plant Evolution
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Organellar data sets confirm overall angiosperm relationships if problematic RNA-edit sites are accounted for in mitochondrial genomes
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Victorin Induction of an Apoptotic/Senescence-Like Response in Oats
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An update of the Angiosperm Phylogeny Group classification for the orders and families of flowering plants: APG IV
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Morphological analysis, phylogenies and classification in Velloziaceae
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Evidence for the involvement of GLOBOSA‐like gene duplications and expression divergence in the evolution of floral morphology in the Zingiberales
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Plastid genomes reveal support for deep phylogenetic relationships and extensive rate variation among palms and other commelinid monocots
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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.
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Inference of phylogenetic relationships among the subfamilies of grasses (Poaceae: Poales) using meso-scale exemplar-based sampling of the plastid genome
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STRUCTURE AND BIOGENESIS OF THE CELL WALLS OF GRASSES
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The Grasses: A Case Study in Macroevolution
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Evolutionary History of Poales
inferred← citeshttps://doi.org/10.1159/000082393openalex-snapshot
The controversial telomeres of lily plants
inferred← citeshttps://doi.org/10.1186/1471-2148-4-35openalex-snapshot
Long branch attraction, taxon sampling, and the earliest angiosperms: Amborella or monocots?
inferred← citeshttps://doi.org/10.1186/s12976-015-0013-2openalex-snapshot
In silico characterization and Molecular modeling of double-strand break repair protein MRE11 from Phoenix dactylifera v deglet nour
inferred← citeshttps://doi.org/10.12705/636.31openalex-snapshot
Molecular phylogenetics and morphology of Beaucarnea (Ruscaceae) as distinct from Nolina , and the submersion of Calibanus into Beaucarnea
inferred← citeshttps://doi.org/10.12705/673.5openalex-snapshot
Nuclear genes, matK and the phylogeny of the Poales
inferred← citeshttps://doi.org/10.13102/scb420openalex-snapshot
Flora da Bahia: Typhaceae
inferred← citeshttps://doi.org/10.1371/journal.pone.0019954openalex-snapshot
A Set of 100 Chloroplast DNA Primer Pairs to Study Population Genetics and Phylogeny in Monocotyledons
inferred← citeshttps://doi.org/10.1590/2175-7860201970021openalex-snapshot
Edmundoa, Neoregelia e Wittrockia (Bromeliaceae: Bromelioideae) no Parque Nacional da Serra dos Órgãos, Rio de Janeiro, Brasil
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1600/0363644054223710openalex-snapshot
DNA Taxonomy—the Riddle of Oxychloë (Juncaceae)
inferred← citeshttps://doi.org/10.1600/036364407781179707openalex-snapshot
Monophyly and Phylogenetic Relationships in Lymania (Bromeliaceae: Bromelioideae) Based on Morphology and Chloroplast DNA Sequences
inferred← citeshttps://doi.org/10.1600/036364409790139619openalex-snapshot
Morphological Phylogenetics of Quesnelia (Bromeliaceae, Bromelioideae)
inferred← citeshttps://doi.org/10.1663/0006-8101(2002)068[0524:spaeom]2.0.co;2openalex-snapshot
Sieve-Element Plastids and Evolution of Monocotyledons, with Emphasis on Melanthiaceae sensu lato and Aristolochiaceae-Asaroideae, a Putative Dicotyledon Sister Group
inferred← citeshttps://doi.org/10.1663/0006-8101(2003)069[0002:stnbed]2.0.co;2openalex-snapshot
Should Taxon Names Be Explicitly Defined?
inferred← citeshttps://doi.org/10.17129/botsci.1509openalex-snapshot
Phylogenetic analysis of large molecular data sets
inferred← citeshttps://doi.org/10.2307/1223578openalex-snapshot
A comparison of traditional and phylogenetic nomenclature
inferred← citeshttps://doi.org/10.2307/1224136openalex-snapshot
Resurrection of Themidaceae for the Brodiaea alliance, and recircumscription of Alliaceae, Amaryllidaceae and Agapanthoideae
inferred← citeshttps://doi.org/10.2307/1224762openalex-snapshot
Toxic Plants of North America
inferred← citeshttps://doi.org/10.2307/1547811openalex-snapshot
Phylogeny of the Vittariaceae: Convergent Simplification Leads to a Polyphyletic Vittaria
inferred← citeshttps://doi.org/10.2307/2399846openalex-snapshot
Phylogenetics of Seed Plants: An Analysis of Nucleotide Sequences from the Plastid Gene rbcL
inferred← citeshttps://doi.org/10.2307/2419449openalex-snapshot
A Chloroplast DNA Study of the Agavaceae
inferred← citeshttps://doi.org/10.2307/2419573openalex-snapshot
The Phylogenetic Position of Prionium (Juncaceae) within the Order Juncales Based on Morphological and rbcL Sequence Data
inferred← citeshttps://doi.org/10.2307/2419806openalex-snapshot
A Phylogenetic Structure for the Monocotyledons, as Inferred from Chloroplast DNA Restriction Site Variation, and a Comparison of Measures of Clade Support
inferred← citeshttps://doi.org/10.2307/2419824openalex-snapshot
A Revised Circumscription of the Genera of the Fern Family Vittariaceae
inferred← citeshttps://doi.org/10.2307/2445819openalex-snapshot
The matK gene: sequence variation and application in plant systematics
inferred← citeshttps://doi.org/10.2307/2445903openalex-snapshot
Examination of subfamilial phylogeny in Bromeliaceae using comparative sequencing of the plastid locus ndhF
inferred← citeshttps://doi.org/10.2307/2446009openalex-snapshot
The fossil monocot Limnobiophyllum scutatum: Resolving the Phylogeny of Lemnaceae
inferred← citeshttps://doi.org/10.2307/2446015openalex-snapshot
The structure and function of RuBisCO and their Implications for Systematic Studies
inferred← citeshttps://doi.org/10.2307/2446206openalex-snapshot
Phylogeny of Agavaceae Based on ITS rDNA Sequence Variation
inferred← citeshttps://doi.org/10.2307/2446365openalex-snapshot
Phylogeny of Podocarpaceae: comparison of Evidence from Morphology and 18s rDNA
inferred← citeshttps://doi.org/10.2307/25065681openalex-snapshot
Are mitochondrial genes useful for the analysis of monocot relationships?
inferred← citeshttps://doi.org/10.2307/2656778openalex-snapshot
Circumscription and phylogeny of the Laurales: evidence from molecular and morphological data
inferred← citeshttps://doi.org/10.2307/2656780openalex-snapshot
Systematics of Amaryllidaceae based on cladistic analysis of plastid sequence data
inferred← citeshttps://doi.org/10.2307/2656790openalex-snapshot
A developmental and evolutionary analysis of embryology in Platanus (platanaceae), abasal eudicot
inferred← citeshttps://doi.org/10.2307/2657094openalex-snapshot
Coding and noncoding plastid DNA in palm systematics
inferred← citeshttps://doi.org/10.2307/2666727openalex-snapshot
Phylogenetic Relationships in the Commelinaceae: I. A. Cladistic Analysis of Morphological Data
inferred← citeshttps://doi.org/10.2307/3558411openalex-snapshot
Generic circumscription and relationships in the tribe Melanthieae (Liliales, Melanthiaceae), with emphasis on Zigadenus: evidence from ITS and trnL‐F sequence data
inferred← citeshttps://doi.org/10.2307/3558433openalex-snapshot
Molecular systematics of Iridaceae: evidence from four plastid DNA regions
inferred← citeshttps://doi.org/10.2307/4118869openalex-snapshot
Taxonomy of Cyanastroideae (Tecophilaeaceae): A Multidisciplinary Approach
inferred← citeshttps://doi.org/10.2307/4135547openalex-snapshot
Recognition of Martellidendron , a new genus of Pandanaceae, and its biogeographic implications
inferred← citeshttps://doi.org/10.24275/uami.1r66j1327openalex-snapshot
Filogenia del género Viridantha Espejo (Bromeliaceae) con base en caracteres morfológicos y moleculares
inferred← citeshttps://doi.org/10.31390/gradschool_theses.2102openalex-snapshot
Palm community development and influence on seedling establishment in a tropical moist forest, Panama
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/d18030174openalex-snapshot
Plastid Genome Characterization and Development of Plastid and Nuclear SNP Markers for Juncus decipiens (Juncaceae)
inferred← citeshttps://doi.org/10.3417/2009130openalex-snapshot
A New Species ofHechtia(Bromeliaceae) from Chihuahua, Mexico
inferred← citeshttps://doi.org/10.3417/2010023openalex-snapshot
Assembling the Tree of the Monocotyledons: Plastome Sequence Phylogeny and Evolution of Poales 1
inferred← citeshttps://doi.org/10.3417/2014014openalex-snapshot
Evolution of Angiosperm Pollen. 3. Monocots1
inferred← citeshttps://doi.org/10.3732/ajb.0800073openalex-snapshot
Phylogenetic relationships of aroids and duckweeds (Araceae) inferred from coding and noncoding plastid DNA
inferred← citeshttps://doi.org/10.3732/ajb.2007310openalex-snapshot
Phylogenetic analyses of two mitochondrial metabolic genes sampled in parallel from angiosperms find fundamental interlocus incongruence
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.3732/ajb.91.10.1645openalex-snapshot
Monocot relationships: an overview
inferred← citeshttps://doi.org/10.3732/ajb.91.3.490openalex-snapshot
Intergeneric and infrafamilial phylogeny of subfamily Monsteroideae (Araceae) revealed by chloroplast <011>trnL‐F sequences
inferred← citeshttps://doi.org/10.3732/ajb.92.2.337openalex-snapshot
Phylogenetic relationships in subfamily Tillandsioideae (Bromeliaceae) based on DNA sequence data from seven plastid regions
inferred← citeshttps://doi.org/10.3732/ajb.93.7.963openalex-snapshot
Origins and nature of vessels in monocotyledons: 8. Orchidaceae
inferred← citeshttps://doi.org/10.3923/pjbs.2023.504.509openalex-snapshot
Research on Passiflora foetida L. as a Pharmaceutical Treatment for Neurasthenia in Humans
inferred← citeshttps://doi.org/10.4314/gjpas.v23i2.2openalex-snapshot
Sequence analysis of Maturase K (matK): A chloroplast-encoding gene in some selected pulses
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