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A Phylogenetic Analysis of Loasaceae Subfamily Loasoideae Based on Plastid DNA Sequences

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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/mpev.1999.0769openalex-snapshot
The Phylogeny of the Asteridae sensu lato Based on Chloroplast ndhF Gene Sequences
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/bf00160154openalex-snapshot
Maximum likelihood phylogenetic estimation from DNA sequences with variable rates over sites: Approximate methods
inferredcites →https://doi.org/10.1007/bf00983214openalex-snapshot
Implications ofrbcL sequence data for higher order relationships of theLoasaceae and the anomalous aquatic plantHydrostachys (Hydrostachyaceae)
inferredcites →https://doi.org/10.1007/bf02101694openalex-snapshot
Dating of the human-ape splitting by a molecular clock of mitochondrial DNA
inferredcites →https://doi.org/10.1016/j.ode.2003.12.001openalex-snapshot
A preliminary phylogeny of Loasaceae subfam. Loasoideae (Angiospermae: Cornales) based on L sequence data, with consequences for systematics and historical biogeography
inferredcites →https://doi.org/10.1016/s0031-9422(98)00744-4openalex-snapshot
Iridoid glucosides—chemotaxonomic markers in Loasoideae
inferredcites →https://doi.org/10.1016/s1055-7903(02)00267-1openalex-snapshot
Relationships within Cornales and circumscription of Cornaceae—matK and rbcL sequence data and effects of outgroups and long branches
inferredcites →https://doi.org/10.1080/106351500750049752openalex-snapshot
Likelihood-Based Tests of Topologies in Phylogenetics
inferredcites →https://doi.org/10.1080/10635150290069922openalex-snapshot
Model Misspecification and Probabilistic Tests of Topology: Evidence from Empirical Data Sets
inferredcites →https://doi.org/10.1080/10635150390235494openalex-snapshot
Performance-Based Selection of Likelihood Models for Phylogeny Estimation
inferredcites →https://doi.org/10.1080/10635150490423520openalex-snapshot
The Importance of Proper Model Assumption in Bayesian Phylogenetics
inferredcites →https://doi.org/10.1086/320789openalex-snapshot
A Phylogenetic Analysis of Hydrangeaceae Based on Sequences of the Plastid Gene matK and Their Combination with rbcL and Morphological Data
inferredcites →https://doi.org/10.1086/376873openalex-snapshot
Homology and Developmental Transformation: Models for the Origins of the Staminodes of Loasaceae Subfamily Loasoideae
inferredcites →https://doi.org/10.1093/bioinformatics/13.3.235openalex-snapshot
Seq-Gen: an application for the Monte Carlo simulation of DNA sequence evolution along phylogenetic trees
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a026201openalex-snapshot
Multiple Comparisons of Log-Likelihoods with Applications to Phylogenetic Inference
inferredcites →https://doi.org/10.1093/sysbio/45.4.546openalex-snapshot
A Likelihood-Ratio Test of Monophyly
inferredcites →https://doi.org/10.1111/j.1558-5646.1983.tb05533.xopenalex-snapshot
PHYLOGENETIC INFERENCE FROM RESTRICTION ENDONUCLEASE CLEAVAGE SITE MAPS WITH PARTICULAR REFERENCE TO THE EVOLUTION OF HUMANS AND THE APES
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/10.2307/2399856openalex-snapshot
Phylogenetic Relationships of Cornus L. Sensu Lato and Putative Relatives Inferred 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/10.2307/2418496openalex-snapshot
Cytotaxonomic Observations in Loasaceae Subfamily Loasoideae
inferredcites →https://doi.org/10.2307/2419163openalex-snapshot
A Reevaluation of Klaprothia and Sclerothrix (Loasaceae: Klaprothieae)
inferredcites →https://doi.org/10.2307/2419252openalex-snapshot
Seed Morphology of Eucnide and Other Loasaceae
inferredcites →https://doi.org/10.2307/2446317openalex-snapshot
Phylogenetic relationships of Cornaceae and close relatives inferred from matK and rbcL sequences
inferredcites →https://doi.org/10.2307/2656658openalex-snapshot
Phytochemistry and the systematics and ecology of Loasaceae and Gronoviaceae (Loasales)
inferredcites →https://doi.org/10.2307/2657022openalex-snapshot
Phylogenetic relationships of Loasaceae subfamily Gronovioideae inferred from matK and ITS sequence data
inferredcites →https://doi.org/10.2307/4118687openalex-snapshot
Notes on Kissenia and the Geographical Distribution of the Loasaceae
inferredcites →https://doi.org/10.3732/ajb.90.8.1215openalex-snapshot
The major clades of Loasaceae: phylogenetic analysis using the plastid matK and trnL‐trnF regions
inferredcites →https://doi.org/10.5281/zenodo.16060396openalex-snapshot
Loasoideae in Eastern South America and on Hispaniola: Names, Types and a Key

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.329.1.3zenodo-depositor-declared
A taxonomic revision of the western South American genus Presliophytum (Loasaceae)
inferred← citeshttps://doi.org/10.11646/phytotaxa.365.3.5zenodo-depositor-declared
An unusual disjunction in Loasaceae: Central American Chichicaste grandis is nested in Brazilian Aosa
inferred← citeshttps://doi.org/10.1002/9780470015902.a0003729.pub2openalex-snapshot
Cornales (Dogwood)
inferred← citeshttps://doi.org/10.1002/ajb2.16455openalex-snapshot
Comparative diversification analyses of Hydrangeaceae and Loasaceae reveal complex evolutionary history as species disperse out of Mesoamerica
inferred← citeshttps://doi.org/10.1002/tax.13289openalex-snapshot
Resolving the early‐diverging clades of Loasaceae subfam. Loasoideae – Segregating the new genus Prosa from the Atacama Desert genus Huidobria
inferred← citeshttps://doi.org/10.1007/s10682-016-9826-7openalex-snapshot
Flower reshaping in the transition to hummingbird pollination in Loasaceae subfam. Loasoideae despite absence of corolla tubes or spurs
inferred← citeshttps://doi.org/10.1007/s13127-016-0312-4openalex-snapshot
Diversification of Caiophora (Loasaceae subfam. Loasoideae) during the uplift of the Central Andes
inferred← citeshttps://doi.org/10.1016/j.sajb.2026.05.035openalex-snapshot
Species and names of Cnidone (Cornales: Loasaceae), the genus formerly known as Kissenia
inferred← citeshttps://doi.org/10.1016/j.ympev.2019.106601openalex-snapshot
Plastid phylogenomics and biogeographic analysis support a trans-Tethyan origin and rapid early radiation of Cornales in the Mid-Cretaceous
inferred← citeshttps://doi.org/10.1016/j.ympev.2019.106616openalex-snapshot
Major lineages of Loasaceae subfam. Loasoideae diversified during the Andean uplift
inferred← citeshttps://doi.org/10.1038/s41598-018-32384-4openalex-snapshot
A case of behavioural diversification in male floral function – the evolution of thigmonastic pollen presentation
inferred← citeshttps://doi.org/10.1055/s-2005-873034openalex-snapshot
Evolution of Funnel-Revolver Flowers and Ornithophily in Nasa (Loasaceae)
inferred← citeshttps://doi.org/10.1093/aob/mcl136openalex-snapshot
Nectar, Floral Morphology and Pollination Syndrome in Loasaceae subfam. Loasoideae (Cornales)
inferred← citeshttps://doi.org/10.1093/aob/mcw035openalex-snapshot
Exploring the ontogenetic scaling hypothesis during the diversification of pollination syndromes inCaiophora(Loasaceae, subfam. Loasoideae)
inferred← citeshttps://doi.org/10.1093/botlinnean/boab010openalex-snapshot
Morphological, ecological and geographical evolution of the Neotropical genusNasa(Loasaceae subfamily Loasoideae)
inferred← citeshttps://doi.org/10.12705/662.5openalex-snapshot
Phylogenetic relationships and generic re‐arrangements in “South Andean Loasas” (Loasaceae)
inferred← citeshttps://doi.org/10.14522/darwiniana.2019.72.858openalex-snapshot
THE FIRST COLLECTION OF PINNASA VOLUBILIS (LOASACEAE) FOR THE FLORA OF ARGENTINA
inferred← citeshttps://doi.org/10.14522/darwiniana.2020.81.880openalex-snapshot
NEW INSIGHTS INTO GRAUSA: REINSTATEMENT, DISTRIBUTION AND AFFINITIES OF LOASA ACAULIS (LOASACEAE, LOASOIDEAE)
inferred← citeshttps://doi.org/10.1600/036364410792495809openalex-snapshot
Effects of Substitution Models on Divergence Time Estimates: Simulations and an Empirical Study of Model Uncertainty Using Cornales
inferred← citeshttps://doi.org/10.1600/036364422x16674054154179openalex-snapshot
A New Endemic Species ofLoasaser.Macrospermae(Loasaceae) from Northern Chile
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/10.2307/25065594openalex-snapshot
Validating subfamily, genus and species names in Loasaceae ( Cornales )
inferred← citeshttps://doi.org/10.3390/plants10112324openalex-snapshot
Stinging Trichomes in Apocynaceae and Their Evolution in Angiosperms
inferred← citeshttps://doi.org/10.3732/ajb.2007403openalex-snapshot
Hybridization and crossability in Caiophora (Loasaceae subfam. Loasoideae): Are interfertile species and inbred populations results of a recent radiation?
inferred← citeshttps://doi.org/10.3897/phytokeys.121.33927openalex-snapshot
A new striking and critically endangered species of Nasa (Loasaceae, Cornales) from North Peru
inferred← citeshttps://doi.org/10.3897/phytokeys.47.8347openalex-snapshot
Plant endemism in the Sierras of Córdoba and San Luis (Argentina): understanding links between phylogeny and regional biogeographical patterns1
inferred← citeshttps://doi.org/10.4067/s0717-66432015000200011openalex-snapshot
Consideraciones sobre la sistemática de las familias y los géneros de plantas vasculares endémicos de Chile
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