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Relationships of the genus Azorella (Apiaceae) and other hydrocotyloids inferred from sequence variation in three plastid markers

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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/j.1537-2197.1977.tb12369.xopenalex-snapshot

POLLEN OF KLOTZSCHIA (UMBELLIFERAE): A POSSIBLE LINK TO ARALIACEAE

inferredcites →https://doi.org/10.1002/j.1537-2197.1996.tb12731.xopenalex-snapshot

Higher level relationships of Apiales (Apiaceae and Araliaceae) based on phylogenetic analysis of rbcL sequences

inferredcites →https://doi.org/10.1006/bojl.2000.0380openalex-snapshot

Angiosperm phylogeny inferred from 18S rDNA, rbcL, and atpB sequences

inferredcites →https://doi.org/10.1006/mpev.2000.0920openalex-snapshot

Relationships among “Ancient Araliads” and Their Significance for the Systematics of Apiales

inferredcites →https://doi.org/10.1007/bf00985737openalex-snapshot

Therps16 intron and the phylogeny of theRubioideae (Rubiaceae)

inferredcites →https://doi.org/10.1007/bf00987959openalex-snapshot

Chloroplastrps16 intron phylogeny of the tribeSileneae (Caryophyllaceae)

inferredcites →https://doi.org/10.1007/bf02344283openalex-snapshot

Phylogenetic relationship of medicinally importantCnidium officinale and Japanese Apiaceae based onrbcL sequences

inferredcites →https://doi.org/10.1016/s0254-6299(15)30220-9openalex-snapshot

Recent advances in understanding Apiales and a revised classification

inferredcites →https://doi.org/10.1016/s1055-7903(02)00240-3openalex-snapshot

Phylogenetics of asterids based on 3 coding and 3 non-coding chloroplast DNA markers and the utility of non-coding DNA at higher taxonomic levels

inferredcites →https://doi.org/10.1017/s0960428601000567openalex-snapshot

RELATIONSHIP OF THE ORDER APIALES TO SUBCLASS ASTERIDAE: A RE-EVALUATION OF MORPHOLOGICAL CHARACTERS BASED ON INSIGHTS FROM MOLECULAR DATA

inferredcites →https://doi.org/10.1017/s0960428601000634openalex-snapshot

TOWARDS AN UNDERSTANDING OF THE PHYLOGENETIC RELATIONSHIPS OF AUSTRALIAN Hydrocotyloideae (Apiaceae)

inferredcites →https://doi.org/10.1080/0028825x.1999.9512628openalex-snapshot

Evolution of Stilbocarpa , a megaherb from New Zealand's sub‐antarctic islands

inferredcites →https://doi.org/10.1111/j.1095-8339.2001.tb01097.xopenalex-snapshot

Phylogeny and classification of Marantaceae

inferredcites →https://doi.org/10.1111/j.1095-8339.2003.00247.xopenalex-snapshot

Evolution in Apiales: nuclear and chloroplast markers together in (almost) perfect harmony

inferredcites →https://doi.org/10.1111/j.1756-1051.2002.tb01915.xopenalex-snapshot

The taxonomic value of fruit structure in the Chinese endemic genus Dickinsia (Apiaceae)

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/b99-086openalex-snapshot

Phylogenetic analysis of chloroplast rps16 intron sequences reveals relationships within the woody southern African Apiaceae subfamily Apioideae

inferredcites →https://doi.org/10.2307/1554966openalex-snapshot

Relationships among genera in Saniculoideae and selected Apioideae (Umbelliferae) inferred from nrITS sequences

inferredcites →https://doi.org/10.2307/2399875openalex-snapshot

Phylogenetic Inference in Saxifragaceae Sensu Stricto and Gilia (Polemoniaceae) Using matK Sequences

inferredcites →https://doi.org/10.2307/2418914openalex-snapshot

The Evolution and Classification of Flowering Plants.

inferredcites →https://doi.org/10.2307/2419610openalex-snapshot

Evolutionary Patterns in Apiaceae: Inferences Based on matK Sequence Data

inferredcites →https://doi.org/10.2307/2446032openalex-snapshot

Clarification of the relationship between Apiaceae and Araliaceae based on matK and rbcL sequence data

inferredcites →https://doi.org/10.2307/2446441openalex-snapshot

Molecular systematics of Apiaceae subfamily Apioideae: phylogenetic analyses of nuclear ribosomal DNA internal transcribed spacer and Plastid rpoC1 intron sequences

inferredcites →https://doi.org/10.2307/25065412openalex-snapshot

Phylogeny of the tribe Cinchoneae (Rubiaceae), its position in Cinchonoideae, and description of a new genus, Ciliosemina

inferredcites →https://doi.org/10.2307/2656619openalex-snapshot

Major lineages within Apiaceae subfamily Apioideae: a comparison of chloroplast restriction site and DNA sequence data

inferredcites →https://doi.org/10.2307/2656687openalex-snapshot

A phylogeny of Apiaceae tribe Scandiceae: evidence from nuclear ribosomal DNA internal transcribed spacer sequences

inferredcites →https://doi.org/10.2307/2656915openalex-snapshot

A phylogeny of the flowering plant family Apiaceae based on chloroplast DNA rpl16 and rpoC1 intron sequences: towards a suprageneric classification of subfamily Apioideae

inferredcites →https://doi.org/10.2307/2666224openalex-snapshot

Phylogenetic Analysis of Asterids Based on Sequences of Four Genes

inferredcites →https://doi.org/10.2307/4111112openalex-snapshot

Re-Establishment of Carapichea (Rubiaceae, Psychotrieae)

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.478.1.1zenodo-depositor-declared

Morphology of pollen in Apiales (Asterids, Eudicots)

inferred← citeshttps://doi.org/10.1002/ajb2.1701openalex-snapshot

A higher‐level nuclear phylogenomic study of the carrot family (Apiaceae)

inferred← citeshttps://doi.org/10.1002/ece3.3206openalex-snapshot

Growth form evolution and hybridization in Senecio (Asteraceae) from the high equatorial Andes

inferred← citeshttps://doi.org/10.1007/s00606-008-0086-zopenalex-snapshot

Ezosciadium (Apiaceae): a taxonomic revision of yet another early diverging South African apioid genus

inferred← citeshttps://doi.org/10.1007/s00606-009-0160-1openalex-snapshot

Evidence from fruit structure supports in general the circumscription of Apiaceae subfamily Azorelloideae

inferred← citeshttps://doi.org/10.1007/s00606-010-0338-6openalex-snapshot

Wood and bark anatomy of Centella: scalariform perforation plates support an affinity with the subfamily Mackinlayoideae (Apiaceae)

inferred← citeshttps://doi.org/10.1007/s00606-022-01833-zopenalex-snapshot

A pentaploid endosperm and a Penaea-type embryo sac are likely synapomorphies of Azorella (Apiaceae, Azorelloideae)

inferred← citeshttps://doi.org/10.1007/s00606-025-01977-8openalex-snapshot

Phylogenetic relationships and molecular identification of Hydrocotyle species in North America (Araliaceae)

inferred← citeshttps://doi.org/10.1007/s12228-016-9446-0openalex-snapshot

Assessing Azorella (Apiaceae) and its allies: Phylogenetics and a new classification

inferred← citeshttps://doi.org/10.1007/s12229-010-9061-9openalex-snapshot

Tropical and Temperate: Evolutionary History of Páramo Flora

inferred← citeshttps://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

inferred← citeshttps://doi.org/10.1016/j.ympev.2009.06.010openalex-snapshot

The demise of subfamily Hydrocotyloideae (Apiaceae) and the re-alignment of its genera across the entire order Apiales

inferred← citeshttps://doi.org/10.1016/j.ympev.2017.01.016openalex-snapshot

Chloroplast and ITS phylogenies to understand the evolutionary history of southern South American Azorella, Laretia and Mulinum (Azorelloideae, Apiaceae)

inferred← citeshttps://doi.org/10.1016/j.ympev.2025.108469openalex-snapshot

Resolving reticulate evolutionary histories of polyploid species of Azorella (Apiaceae) endemic to New Zealand

inferred← citeshttps://doi.org/10.1093/aob/mcq084openalex-snapshot

False paracarpy in Seemannaralia (Araliaceae): from bilocular ovary to unilocular fruit

inferred← citeshttps://doi.org/10.1093/aob/mcs204openalex-snapshot

The phylogenetic significance of the carpophore in Apiaceae

inferred← citeshttps://doi.org/10.1111/j.1365-2699.2007.01757.xopenalex-snapshot

The Austral floristic realm revisited

inferred← citeshttps://doi.org/10.1111/jbi.15161openalex-snapshot

So Young, So Rich: Habitat Shifts Combined With Trait Evolution Promoted Species Radiation in Senecio in the Andes

inferred← citeshttps://doi.org/10.1111/jse.13170openalex-snapshot

Tracing the biogeographic history of the world's most isolated insular floras

inferred← citeshttps://doi.org/10.1111/nph.70824openalex-snapshot

Climate adaptation and functional constraints drive pollen evolution in Apiales

inferred← citeshttps://doi.org/10.1371/journal.pone.0020552openalex-snapshot

DNA Barcode Sequence Identification Incorporating Taxonomic Hierarchy and within Taxon Variability

inferred← citeshttps://doi.org/10.1600/036364416x691821openalex-snapshot

Domeykoa andina (Apiaceae; Azorelloideae), a New Species from Northern Chile

inferred← citeshttps://doi.org/10.1600/036364416x692370openalex-snapshot

Morphology, Fruit Anatomy and Taxonomy of the South Andean Genus Laretia (Azorelloideae, Apiaceae)

inferred← citeshttps://doi.org/10.1663/0006-8101(2007)73[67:aucotc]2.0.co;2openalex-snapshot

An Updated Classification of the Class Magnoliopsida (“Angiospermae”)

inferred← citeshttps://doi.org/10.21203/rs.3.rs-1645824/v1openalex-snapshot

A pentaploid endosperm and a Penaea-type embryo sac are likely synapomorphies of Azorella (Apiaceae, Azorelloideae)

inferred← citeshttps://doi.org/10.3732/ajb.1100006openalex-snapshot

Molecular phylogenetic analysis of the Persea group (Lauraceae) and its biogeographic implications on the evolution of tropical and subtropical Amphi‐Pacific disjunctions

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