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New insights into the phylogeny and taxonomy of Chinese Physospermopsis (Apiaceae)

https://doi.org/10.3897/phytokeys.175.57681
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Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/fedr.20001110717openalex-snapshot
Taxonomic revision ofPleurospermumHoffm. and related genera of Umbelliferae I. General part
inferredcites →https://doi.org/10.1002/fedr.20001110718openalex-snapshot
Taxonomic revision of Pleurospermum Hoffm. and related genera of Umbelliferae II. The genera Pleurospermum, Pterocyclus, Trachydium, Keraymonia, Pseudotrachydium, Aulacospermum, and Hymenolaena
inferredcites →https://doi.org/10.1002/fedr.20001110719openalex-snapshot
Taxonomic revision of Pleurospermum Hoffm. and related genera of Umbelliferae III. The genera Physospermopsis and Hymenidium
inferredcites →https://doi.org/10.1002/fedr.4870270109openalex-snapshot
Umbelliferae Asiaticae novae relictae descriptae
inferredcites →https://doi.org/10.1002/j.1537-2197.1996.tb12724.xopenalex-snapshot
Low Levels of Intraspecific Genetic Variation at a Rapidly Evolving Chloroplast DNA Locus in North American Duckweeds (Lemnaceae)
inferredcites →https://doi.org/10.1002/tax.583004openalex-snapshot
Generic delimitations within the Sium alliance (Apiaceae tribe Oenantheae) inferred from cpDNA rps16 ‐5′ trnK (UUU) and nrDNA ITS sequences
inferredcites →https://doi.org/10.1006/mpev.1997.0432openalex-snapshot
Molecular Evolution and Phylogenetic Utility of the Chloroplastrpl16Intron inChusqueaand the Bambusoideae (Poaceae)
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/j.ympev.2009.05.029openalex-snapshot
Towards a more robust molecular phylogeny of Chinese Apiaceae subfamily Apioideae: Additional evidence from nrDNA ITS and cpDNA intron (rpl16 and rps16) sequences
inferredcites →https://doi.org/10.1016/j.ympev.2014.09.028openalex-snapshot
Chloroplast capture and intra- and inter-continental biogeographic diversification in the Asian – New World disjunct plant genus Osmorhiza (Apiaceae)
inferredcites →https://doi.org/10.1016/s0968-0004(98)01285-7openalex-snapshot
Multiple sequence alignment with Clustal X
inferredcites →https://doi.org/10.1080/00378941.1906.10831901openalex-snapshot
LeLinaria pallidasubspontané en Suisse
inferredcites →https://doi.org/10.1093/bioinformatics/btu033openalex-snapshot
RAxML version 8: a tool for phylogenetic analysis and post-analysis of large phylogenies
inferredcites →https://doi.org/10.1093/botlinnean/boy055openalex-snapshot
Taxonomy of the traditional medicinal plant genus Ferula (Apiaceae) is confounded by incongruence between nuclear rDNA and plastid DNA
inferredcites →https://doi.org/10.1093/molbev/msw054openalex-snapshot
MEGA7: Molecular Evolutionary Genetics Analysis Version 7.0 for Bigger Datasets
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/10.1109/tac.1974.1100705openalex-snapshot
A new look at the statistical model identification
inferredcites →https://doi.org/10.1111/j.1095-8339.1892.tb02268.xopenalex-snapshot
Observations on a Botanical Collection made by Mr. A. E. Pratt in Western China, with Descriptions of some new Chinese Plants from various Collections.
inferredcites →https://doi.org/10.1111/j.1744-7909.2005.00141.xopenalex-snapshot
Creation of Transgenic Bananas Expressing Human Lysozyme Gene for Panama Wilt Resistance
inferredcites →https://doi.org/10.1127/1869-6155/2010/0128-0005openalex-snapshot
Major clades within Apiaceae subfamily Apioideae as inferred by phylogenetic analysis of nrDNA ITS sequences
inferredcites →https://doi.org/10.1139/b00-029openalex-snapshot
Molecular systematics of Old World Apioideae (Apiaceae): relationships among some members of tribe Peucedaneae sensu lato, the placement of several island-endemic species, and resolution within the apioid superclade
inferredcites →https://doi.org/10.1139/b06-016openalex-snapshot
Phylogenetic relationships within Cicuta (Apiaceae tribe Oenantheae) inferred from nuclear rDNA ITS and cpDNA sequence data
inferredcites →https://doi.org/10.1139/b99-086openalex-snapshot
Phylogenetic analysis of chloroplast rps16 intron sequences reveals relationships within the woody southern African Apiaceae subfamily Apioideae
inferredcites →https://doi.org/10.11646/phytotaxa.376.1.1openalex-snapshot
Phylogeny of Chinese Chamaesium (Apiaceae: Apioideae) inferred from ITS, cpDNA and morphological characters
inferredcites →https://doi.org/10.1186/1471-2148-7-214openalex-snapshot
BEAST: Bayesian evolutionary analysis by sampling trees
inferredcites →https://doi.org/10.12705/653.9openalex-snapshot
A tool for the analysis of chromosomes: KaryoType
inferredcites →https://doi.org/10.1385/1-59259-192-2:71openalex-snapshot
DNASTAR's Lasergene Sequence Analysis Software
inferredcites →https://doi.org/10.14258/turczaninowia.20.2.9openalex-snapshot
Updated checklist of Chinese Umbelliferae: nomenclature, synonymy, typification, distribution
inferredcites →https://doi.org/10.1600/036364411x583745openalex-snapshot
A Phylogenetic and Biogeographic Study of the Genus Lilaeopsis (Apiaceae tribe Oenantheae)
inferredcites →https://doi.org/10.1600/036364412x635593openalex-snapshot
Broad Polyphyly in Pleurospermum s. l. (Umbelliferae-Apioideae) as Inferred from nrDNA ITS and Chloroplast Sequences
inferredcites →https://doi.org/10.2307/1224129openalex-snapshot
Vascular Plants of the Hengduan Mountains
inferredcites →https://doi.org/10.2307/25066012openalex-snapshot
A molecular phylogeny of Chinese Apiaceae subfamily Apioideae inferred from nuclear ribosomal DNA internal transcribed spacer sequences
inferredcites →https://doi.org/10.2307/3994550openalex-snapshot
Neue Umbelliferen-Gattungen aus Ostasien
inferredcites →https://doi.org/10.3732/ajb.93.12.1828openalex-snapshot
A molecular phylogenetic study of southern African Apiaceae
inferredcites →https://doi.org/10.5169/seals-879801openalex-snapshot
Apiaceae himalayenses : III

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Of the 44 inferred citing records listed on this page, 34 match the GBIF occurrence-download DOI prefix (10.15468/dl.).

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Circumscription of the East Asia clade (Apiaceae subfamily Apioideae) and the taxonomic placements of several problematic genera
inferred← citeshttps://doi.org/10.1016/j.ympev.2026.108699openalex-snapshot
Phylogenomics and morphological evidence reveal a new genus Callibractia gen. Nov. (Apiaceae, Apioideae), a distinct alpine lineage of Sino-Himalaya shaped by uplift of the Pan-Tibetan Highlands
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The complete chloroplast genome sequence of Pittosporum illicioides Makino, 1900 (Pittosporaceae)
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Phylogenetic position of Ligusticopsis (Apiaceae, Apioideae): evidence from molecular data and carpological characters
inferred← citeshttps://doi.org/10.1093/botlinnean/boaf029openalex-snapshot
Taxonomy of the Chinese Ligusticum s.l. revisited by molecular data and mericarp morphology
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The complete plastomes of thirteen Libanotis (Apiaceae, Apioideae) plants: comparative and phylogenetic analyses provide insights into the plastome evolution and taxonomy of Libanotis
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inferred← citeshttps://doi.org/10.3389/fpls.2023.1148303openalex-snapshot
Backbone phylogeny and adaptive evolution of Pleurospermum s. l.: New insights from phylogenomic analyses of complete plastome data
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Plastid phylogenomics contributes to the taxonomic revision of taxa within the genus Sanicula L. and acceptance of two new members of the genus
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Tongoloa cuneata, A New Combination Separated from Physospermopsis s. lato (Apiaceae)
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Additional file 1 of The complete plastomes of thirteen Libanotis (Apiaceae, Apioideae) plants: comparative and phylogenetic analyses provide insights into the plastome evolution and taxonomy of Libanotis
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