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Molecular phylogeny, genome sizes and chromosome numbers in melic grasses and its relatives (Pooideae, Poaceae) with a revised classification of the genus Melica

https://doi.org/10.1002/tax.70050
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What this work says

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

inferredcites →https://doi.org/10.1002/9781119312994.apr0622openalex-snapshot
Evolution and Taxonomy of the Grasses (Poaceae): A Model Family for the Study of Species‐Rich Groups
inferredcites →https://doi.org/10.1002/fedr.19280250702openalex-snapshot
Monographie der südamerikanischen Arten der Gattung Melica L
inferredcites →https://doi.org/10.1002/fedr.19700810111openalex-snapshot
Taxonomische und chorologische Untersuchungen an Arten von Melica L. Subgen. Melica
inferredcites →https://doi.org/10.1002/fedr.19710811002openalex-snapshot
Die systematische Stellung von Melica uniflora Retz. und Melica rectiflora Boiss. er Heldr. (Melica L. Subgen. Bulbimelica, subgen. nov.) (Vorarbeiten zu einer Revision der Gattung Melica L.–I)
inferredcites →https://doi.org/10.1002/fedr.19710811003openalex-snapshot
Die Verwandtschaft der Gattungen Molinia Schrank, Moliniopsis Hayata und Schizachne Hack. mit dem Formenkreis Melica L. Subgen. Bulbimelica Hempel (Vorarbeiten zu einer Revision der Gattung Melica L. – II)
inferredcites →https://doi.org/10.1002/fedr.19730840704openalex-snapshot
Die systematische Stellung von Melica altissima L. und des Melica minuta L.‐Melica ramosa Vill.‐Komplexes (Melica L. Subgen. Altimelica Hempel) (Vorarbeiten zu einer Revision der Gattung Melica L. — III)
inferredcites →https://doi.org/10.1002/fedr.201100029openalex-snapshot
Revision und Phylogenie der Arten der Gattung Melica L. (Poaceae) in Eurasien und Nordafrika
inferredcites →https://doi.org/10.1002/tax.582008openalex-snapshot
Phylogenetic structure of the grass subfamily Pooideae based on comparison of plastid matK gene–3′ trnK exon and nuclear ITS sequences
inferredcites →https://doi.org/10.1002/tax.611002openalex-snapshot
Systematics and evolution of the needle grasses (Poaceae: Pooideae: Stipeae) based on analysis of multiple chloroplast loci, ITS, and lemma micromorphology
inferredcites →https://doi.org/10.1006/anbo.1998.0783openalex-snapshot
Phylogenetic Analysis of DNA C-values provides Evidence for a Small Ancestral Genome Size in Flowering Plants
inferredcites →https://doi.org/10.1006/mpev.2001.0941openalex-snapshot
Molecular Analysis of Phylogenetic Relationships among Myrmecophytic Macaranga Species (Euphorbiaceae)
inferredcites →https://doi.org/10.1007/978-1-0716-3389-2_10openalex-snapshot
The Chromosome Counts Database (CCDB)
inferredcites →https://doi.org/10.1007/978-3-7091-1160-4_19openalex-snapshot
Genome Size Diversity and Evolution in Land Plants
inferredcites →https://doi.org/10.1007/978-3-7091-1160-4_9openalex-snapshot
Mechanisms of Chromosome Rearrangements
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/bf00986805openalex-snapshot
Application of Giemsa banding to orchid karyotype analysis
inferredcites →https://doi.org/10.1007/bf02858328openalex-snapshot
The system of grasses (Poaceae) and their evolution
inferredcites →https://doi.org/10.1007/s00606-024-01934-xopenalex-snapshot
Genome sizes of grasses (Poaceae), chromosomal evolution, paleogenomics and the ancestral grass karyotype (AGK)
inferredcites →https://doi.org/10.1007/s00606-025-01946-1openalex-snapshot
Reductional dysploidy and genome size diversity in Pooideae, the largest subfamily of grasses (Poaceae)
inferredcites →https://doi.org/10.1007/s11104-013-1794-xopenalex-snapshot
Small genomes dominate in plants growing on serpentine soils in West Balkans, an exhaustive study of 8 habitats covering 308 taxa
inferredcites →https://doi.org/10.1016/j.cpb.2020.100181openalex-snapshot
Antagonistic effects of whole-genome duplications and dysploidy on genome sizes in the pantropical monocot family Marantaceae: Consequences in the light of a new molecular phylogeny
inferredcites →https://doi.org/10.1016/j.molp.2022.01.015openalex-snapshot
A well-supported nuclear phylogeny of Poaceae and implications for the evolution of C4 photosynthesis
inferredcites →https://doi.org/10.1016/j.tplants.2016.06.003openalex-snapshot
Genome Stability and Evolution: Attempting a Holistic View
inferredcites →https://doi.org/10.1016/j.tplants.2017.09.011openalex-snapshot
Mixed-Ploidy Species: Progress and Opportunities in Polyploid Research
inferredcites →https://doi.org/10.1016/j.ympev.2015.03.010openalex-snapshot
A multi-locus analysis of phylogenetic relationships within grass subfamily Pooideae (Poaceae) inferred from sequences of nuclear single copy gene regions compared with plastid DNA
inferredcites →https://doi.org/10.1016/j.ympev.2021.107110openalex-snapshot
A 313 plastome phylogenomic analysis of Pooideae: Exploring relationships among the largest subfamily of grasses
inferredcites →https://doi.org/10.1038/ng.807openalex-snapshot
The Arabidopsis lyrata genome sequence and the basis of rapid genome size change
inferredcites →https://doi.org/10.1038/nprot.2007.310openalex-snapshot
Estimation of nuclear DNA content in plants using flow cytometry
inferredcites →https://doi.org/10.1038/nrg.2017.26openalex-snapshot
The evolutionary significance of polyploidy
inferredcites →https://doi.org/10.1038/nrg2600openalex-snapshot
The evolutionary significance of ancient genome duplications
inferredcites →https://doi.org/10.1073/pnas.0904339106openalex-snapshot
Rapid DNA loss as a counterbalance to genome expansion through retrotransposon proliferation in plants
inferredcites →https://doi.org/10.1073/pnas.95.5.2005openalex-snapshot
Relationships of cereal crops and other grasses
inferredcites →https://doi.org/10.1080/14772000.2010.544339openalex-snapshot
Duthieeae, a new tribe of grasses (Poaceae) identified among the early diverging lineages of subfamily Pooideae: molecular phylogenetics, morphological delineation, cytogenetics and biogeography
inferredcites →https://doi.org/10.1080/17550870802331912openalex-snapshot
Temporal patterns of evolution in the Arctic explored inArtemisiaL. (Asteraceae) lineages of different age
inferredcites →https://doi.org/10.1080/23802359.2019.1660258openalex-snapshot
The complete chloroplast genome sequence of Melica scabrosa (Poaceae)
inferredcites →https://doi.org/10.1086/346168openalex-snapshot
Potential of the 5′ and 3′ Ends of the Intergenic Spacer (IGS) of rDNA in the Cyperaceae: New Sequences for Lower‐Level Phylogenies in Sedges with an Example from Uncinia Pers.
inferredcites →https://doi.org/10.1086/700636openalex-snapshot
Polyploidy, the Nucleotype, and Novelty: The Impact of Genome Doubling on the Biology of the Cell
inferredcites →https://doi.org/10.1093/aob/mcab102openalex-snapshot
The nature of intraspecific and interspecific genome size variation in taxonomically complex eyebrights
inferredcites →https://doi.org/10.1093/aob/mcac151openalex-snapshot
Diverse mangroves deviate from other angiosperms in their genome size, leaf cell size and cell packing density relationships
inferredcites →https://doi.org/10.1093/aob/mcad136openalex-snapshot
Melica as an emerging model system for comparative studies in temperate Pooideae grasses
inferredcites →https://doi.org/10.1093/aob/mci019openalex-snapshot
The Origin, Evolution and Proposed Stabilization of the Terms 'Genome Size' and 'C-Value' to Describe Nuclear DNA Contents
inferredcites →https://doi.org/10.1093/aobpla/plv046openalex-snapshot
Plastid phylogenomics of the cool-season grass subfamily: clarification of relationships among early-diverging tribes
inferredcites →https://doi.org/10.1093/bfgp/elu005openalex-snapshot
Plant genome size variation: bloating and purging DNA
inferredcites →https://doi.org/10.1093/biolinnean/blad070openalex-snapshot
Correlations among chromosome numbers, nuclear DNA contents and climatic variables of South American Cactaceae in a phylogenetic context
inferredcites →https://doi.org/10.1093/botlinnean/boae041openalex-snapshot
The migration history of the Kamchatka rhododendron (Therorhodion camtschaticum s.l.) indicates two distinct dispersal routes towards Eastern Beringia
inferredcites →https://doi.org/10.1093/jxb/erac149openalex-snapshot
Major niche transitions in Pooideae correlate with variation in photoperiodic flowering and evolution of CCT domain genes
inferredcites →https://doi.org/10.1093/molbev/msac026openalex-snapshot
Phylotranscriptomics Resolves the Phylogeny of Pooideae and Uncovers Factors for Their Adaptive Evolution
inferredcites →https://doi.org/10.1093/molbev/mst010openalex-snapshot
MAFFT Multiple Sequence Alignment Software Version 7: Improvements in Performance and Usability
inferredcites →https://doi.org/10.1093/molbev/msz189openalex-snapshot
ModelTest-NG: A New and Scalable Tool for the Selection of DNA and Protein Evolutionary Models
inferredcites →https://doi.org/10.1093/nsr/nwz035openalex-snapshot
Asymmetric biotic interchange across the Bering land bridge between Eurasia and North America
inferredcites →https://doi.org/10.1093/plcell/koaa015openalex-snapshot
Polyploidy: an evolutionary and ecological force in stressful times
inferredcites →https://doi.org/10.1093/sysbio/sys029openalex-snapshot
MrBayes 3.2: Efficient Bayesian Phylogenetic Inference and Model Choice Across a Large Model Space
inferredcites →https://doi.org/10.1101/gr.5282906openalex-snapshot
Differential lineage-specific amplification of transposable elements is responsible for genome size variation in Gossypium
inferredcites →https://doi.org/10.1101/gr.5290206openalex-snapshot
Doubling genome size without polyploidization: Dynamics of retrotransposition-driven genomic expansions in Oryza australiensis , a wild relative of rice
inferredcites →https://doi.org/10.1105/tpc.9.9.1509openalex-snapshot
Do Plants Have a One-Way Ticket to Genomic Obesity?
inferredcites →https://doi.org/10.1111/j.1469-8137.2011.03972.xopenalex-snapshot
New grass phylogeny resolves deep evolutionary relationships and discovers C 4 origins
inferredcites →https://doi.org/10.1111/j.1558-5646.2007.00270.xopenalex-snapshot
PARALLEL EVOLUTIONARY PATTERNS IN MULTIPLE LINEAGES OF ARCTIC ARTEMISIA L. (ASTERACEAE)
inferredcites →https://doi.org/10.1111/jse.12150openalex-snapshot
A worldwide phylogenetic classification of the Poaceae (Gramineae)
inferredcites →https://doi.org/10.1111/jse.12222openalex-snapshot
Intercontinental disjunctions between eastern Asia and western North America in vascular plants highlight the biogeographic importance of the Bering land bridge from late Cretaceous to Neogene
inferredcites →https://doi.org/10.1111/jse.12262openalex-snapshot
A worldwide phylogenetic classification of the Poaceae (Gramineae) II: An update and a comparison of two 2015 classifications
inferredcites →https://doi.org/10.1111/jse.12302openalex-snapshot
The role of land bridges, ancient environments, and migrations in the assembly of the North American flora
inferredcites →https://doi.org/10.1111/jse.12847openalex-snapshot
A worldwide phylogenetic classification of the Poaceae (Gramineae) III: An update
inferredcites →https://doi.org/10.1111/jse.12857openalex-snapshot
Grasses through space and time: An overview of the biogeographical and macroevolutionary history of Poaceae
inferredcites →https://doi.org/10.1111/jse.13174openalex-snapshot
East Asia–eastern North America disjunction revisited: Possible westward colonization route via the Western Palearctic in Carex sect. Paniceae (Cyperaceae)
inferredcites →https://doi.org/10.1111/nph.13191openalex-snapshot
The Chromosome Counts Database ( CCDB ) – a community resource of plant chromosome numbers
inferredcites →https://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
inferredcites →https://doi.org/10.1111/nph.16666openalex-snapshot
Increased above‐ground resource allocation is a likely precursor for independent evolutionary origins of annuality in the Pooideae grass subfamily
inferredcites →https://doi.org/10.1111/nph.20263openalex-snapshot
A nuclear phylogenomic tree of grasses (Poaceae) recovers current classification despite gene tree incongruence
inferredcites →https://doi.org/10.1155/2010/862516openalex-snapshot
Genome Size Dynamics and Evolution in Monocots
inferredcites →https://doi.org/10.1186/1471-2148-6-62openalex-snapshot
Retrotranspositions in orthologous regions of closely related grass species
inferredcites →https://doi.org/10.1186/1471-2229-10-265openalex-snapshot
Correlated evolution of LTR retrotransposons and genome size in the genus eleocharis
inferredcites →https://doi.org/10.1371/journal.pone.0192869openalex-snapshot
Karyotype evolution in Phalaris (Poaceae): The role of reductional dysploidy, polyploidy and chromosome alteration in a wide-spread and diverse genus
inferredcites →https://doi.org/10.17816/ecogen9463-69openalex-snapshot
The ITS1-5.8S rRNA gene -ITS2 sequence variability during the divergence of sweet-grass species (gen us Glyceria R. Br.)
inferredcites →https://doi.org/10.2135/cropsci2004.0604openalex-snapshot
Evolution of Genome Size in the Grasses
inferredcites →https://doi.org/10.2307/1223481openalex-snapshot
Flora of North America North of Mexico
inferredcites →https://doi.org/10.2307/2399224openalex-snapshot
Polyploidy, Hybridization, and the Invasion of New Habitats
inferredcites →https://doi.org/10.2307/25065407openalex-snapshot
The Families and Genera of Vascular Plants
inferredcites →https://doi.org/10.2307/2807332openalex-snapshot
Genera Graminum. Grasses of the World.
inferredcites →https://doi.org/10.2307/2807477openalex-snapshot
Grass Systematics and Evolution.
inferredcites →https://doi.org/10.2307/3298585openalex-snapshot
Phylogeny and Subfamilial Classification of the Grasses (Poaceae)
inferredcites →https://doi.org/10.23855/preslia.2019.117openalex-snapshot
Genome sizes and genomic guanine+cytosine (GC) contents of the Czech vascular flora with new estimates for 1700 species
inferredcites →https://doi.org/10.3264/fg.2019.1022openalex-snapshot
The DNA weights per nucleus (genome size) of more than 2350 species of the Flora of The Netherlands, of which 1370 are new to science, including the pattern of their DNA peaks
inferredcites →https://doi.org/10.3389/fpls.2022.901733openalex-snapshot
Evolutionary Dynamics of the Repeatome Explains Contrasting Differences in Genome Sizes and Hybrid and Polyploid Origins of Grass Loliinae Lineages
inferredcites →https://doi.org/10.3389/fpls.2024.1419255openalex-snapshot
Expansions and contractions of repetitive DNA elements reveal contrasting evolutionary responses to the polyploid genome shock hypothesis in Brachypodium model grasses
inferredcites →https://doi.org/10.3390/biology11050636openalex-snapshot
A Reappraisal of Polyploidy Events in Grasses (Poaceae) in a Rapidly Changing World
inferredcites →https://doi.org/10.3390/genes9020088openalex-snapshot
Genome Size Diversity and Its Impact on the Evolution of Land Plants
inferredcites →https://doi.org/10.3732/ajb.0900228openalex-snapshot
Migration of endpoints of two genes relative to boundaries between regions of the plastid genome in the grass family (Poaceae)
inferredcites →https://doi.org/10.3732/ajb.91.10.1709openalex-snapshot
The evolution of nuclear genome structure in seed plants
inferredcites →https://doi.org/10.4103/ijpvm.ijpvm_200_22openalex-snapshot
The "P"-Value: The Primary Alphabet of Research Revisited
inferredcites →https://doi.org/10.54830/bmnhn.v40.1984.434openalex-snapshot
Revisión de las especies chilenas del genero Mélica L. (Gramineae)
inferredcites →https://doi.org/10.5642/aliso.20072301.02openalex-snapshot
Table of Contents
inferredcites →https://doi.org/10.5860/choice.38-2737openalex-snapshot
Grasses: systematics and evolution
inferredcites →https://doi.org/10.5962/bhl.title.64674openalex-snapshot
The genera of grasses of the United States : with special reference to the economic species
inferredcites →https://doi.org/10.7717/peerj.3815openalex-snapshot
Are diversification rates and chromosome evolution in the temperate grasses (Pooideae) associated with major environmental changes in the Oligocene-Miocene?
inferredcites →https://doi.org/10.7717/peerj.4299openalex-snapshot
A 250 plastome phylogeny of the grass family (Poaceae): topological support under different data partitions

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

inferred← citeshttps://doi.org/10.5091/plecevo.204621zenodo-depositor-declared
Morphological and molecular evidence for a new endemic species of Triniochloa (Poaceae) from Jalisco, Mexico
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