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Hybridization and crossability in Caiophora (Loasaceae subfam. Loasoideae): Are interfertile species and inbred populations results of a recent radiation?
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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.1537-2197.1979.tb06321.xopenalex-snapshot
BIOSYSTEMATICS OF THE GENUS HYDROPHYLLUM L. (HYDROPHYLLACEAE)
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Relationships between African species of the genus Cucumis L. Estimated by the production, vigour and fertility of F1 hybrids
inferredcites →https://doi.org/10.1007/bf00936094openalex-snapshot
Hybridization studies in the genusSilene sectt.Siphonomorpha andAuriculatae (Caryophyllaceae)
inferredcites →https://doi.org/10.1007/bf01725743openalex-snapshot
Interspecific hybridization inRibes
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Plant genetic differences influence herbivore community structure: evidence from a hybrid willow system
inferredcites →https://doi.org/10.1007/s006060170008openalex-snapshot
Natural hybridization between species of Calceolaria with different pollination syndromes in southern Patagonia, Argentina
inferredcites →https://doi.org/10.1016/j.biocon.2007.02.004openalex-snapshot
Interspecific hybridisation between alien and native plant species in Germany and its consequences for native biodiversity
inferredcites →https://doi.org/10.1016/j.flora.2005.06.009openalex-snapshot
The seeds of Loasaceae subfam. Loasoideae (Cornales) II: Seed morphology of “South Andean Loasas” (Loasa, Caiophora, Scyphanthus and Blumenbachia)
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/10.1023/a:1026194227110openalex-snapshot
Hard X-rays, ejecta, and their associated decimetric radio emission in solar flares
inferredcites →https://doi.org/10.1038/sj.hdy.6800687openalex-snapshot
Hybrid zones between invasive Rorippa austriaca and native R. sylvestris (Brassicaceae) in Germany: ploidy levels and patterns of fitness in the field
inferredcites →https://doi.org/10.1046/j.1365-294x.2003.01854.xopenalex-snapshot
Hybridization andRorippa austriaca(Brassicaceae) invasion in Germany
inferredcites →https://doi.org/10.1046/j.1469-8137.2003.00919.xopenalex-snapshot
Natural selection in Ipomopsis hybrid zones: implications for ecological speciation
inferredcites →https://doi.org/10.1049/ic:19950209openalex-snapshot
Teaching real-time DSP using digital signal processors at the University of Leicester
inferredcites →https://doi.org/10.1055/s-2005-873034openalex-snapshot
Evolution of Funnel-Revolver Flowers and Ornithophily in Nasa (Loasaceae)
inferredcites →https://doi.org/10.1073/pnas.0510270103openalex-snapshot
High biological species diversity in the arctic flora
inferredcites →https://doi.org/10.1073/pnas.0601928103openalex-snapshot
Island radiation on a continental scale: Exceptional rates of plant diversification after uplift of the Andes
inferredcites →https://doi.org/10.1073/pnas.2237235100openalex-snapshot
Genetic introgression as a potential to widen a species' niche: Insights from alpine Carex curvula
inferredcites →https://doi.org/10.1073/pnas.93.10.5090openalex-snapshot
Distribution of spontaneous plant hybrids.
inferredcites →https://doi.org/10.1078/0367-2530-00170openalex-snapshot
The seeds of Loasaceae subfam. Loasoideae (Cornales) I: Seed release, seed numbers and fatty acid composition
inferredcites →https://doi.org/10.1086/427477openalex-snapshot
A Phylogenetic Analysis of Loasaceae Subfamily Loasoideae Based on Plastid DNA Sequences
inferredcites →https://doi.org/10.1093/aob/mcl136openalex-snapshot
Nectar, Floral Morphology and Pollination Syndrome in Loasaceae subfam. Loasoideae (Cornales)
inferredcites →https://doi.org/10.1093/genetics/150.3.1209openalex-snapshot
Genetics of Adaptive Radiation in Hawaiian and Cook Islands Species of Tetramolopium (Asteraceae). II. Genetic Linkage Map and Its Implications for Interspecific Breeding Barriers
inferredcites →https://doi.org/10.1098/rspb.2000.1578openalex-snapshot
Asymmetrical crossing barriers in angiosperms
inferredcites →https://doi.org/10.1111/j.0014-3820.2000.tb00551.xopenalex-snapshot
POPULATION DIFFERENTIATION IN AN ANNUAL LEGUME: GENETIC ARCHITECTURE
inferredcites →https://doi.org/10.1111/j.0014-3820.2003.tb00360.xopenalex-snapshot
COMPONENTS OF REPRODUCTIVE ISOLATION BETWEEN THE MONKEYFLOWERS MIMULUS LEWISII AND M. CARDINALIS (PHRYMACEAE)
inferredcites →https://doi.org/10.1111/j.0014-3820.2006.tb01092.xopenalex-snapshot
HETEROSIS IN AN ISOLATED, EFFECTIVELY SMALL, AND SELF-FERTILIZING POPULATION OF THE FLOWERING PLANT LEAVENWORTHIA ALABAMICA
inferredcites →https://doi.org/10.1111/j.1365-294x.2005.02670.xopenalex-snapshot
Asymmetrical introgression between twoMorusspecies (M. alba,M. rubra) that differ in abundance
inferredcites →https://doi.org/10.1111/j.1420-9101.2005.00965.xopenalex-snapshot
Inbreeding depression and heterosis in populations of Schiedea viscosa, a highly selfing species
inferredcites →https://doi.org/10.1111/j.1420-9101.2005.01067.xopenalex-snapshot
Increased ecological amplitude through heterosis following wide outcrossing in Banksia ilicifolia R.Br. (Proteaceae)
inferredcites →https://doi.org/10.1111/j.1438-8677.1997.tb00626.xopenalex-snapshot
Micro‐Foraging Routes of Bicolletes pampeana (Colletidae) and Bee‐Induced Pollen Presentation in Cajophora arechavaletae (Loasaceae)
inferredcites →https://doi.org/10.1111/j.1558-5646.1958.tb02954.xopenalex-snapshot
CROSSING RELATIONSHIPS IN THE GENUS CARICA
inferredcites →https://doi.org/10.1111/j.1558-5646.1997.tb03958.xopenalex-snapshot
THE EFFECT OF HABITAT ON PARENTAL AND HYBRID FITNESS: TRANSPLANT EXPERIMENTS WITH LOUISIANA IRISES
inferredcites →https://doi.org/10.1111/j.1601-5223.1928.tb02491.xopenalex-snapshot
CYTOLOGICAL STUDIES IN THE GENUS RIBES L
inferredcites →https://doi.org/10.1111/j.1601-5223.1964.tb01945.xopenalex-snapshot
CYTOLOGISCHE UNTERSUCHUNGEN AN TETRAPLOIDEN PFLANZEN DER GATTUNG RIBES L.
inferredcites →https://doi.org/10.1146/annurev.genet.35.102401.085719openalex-snapshot
Genetics and the Fitness of Hybrids
inferredcites →https://doi.org/10.21273/hortsci.40.3.532openalex-snapshot
Artificial Hybridizations in Five Species of Chilean Nolana (Solanaceae)
inferredcites →https://doi.org/10.2307/2398789openalex-snapshot
The Systematics and Evolution of Fuchsia Sect. Fuchsia (onagraceae)
inferredcites →https://doi.org/10.2307/2399500openalex-snapshot
Observations on Polyploidy in Fuchsia Sects. Quelusia and Kierschlegeria (Onagraceae)
inferredcites →https://doi.org/10.2307/2418372openalex-snapshot
Artificial Hybridization Among Species of Chenopodium sect. Chenopodium
inferredcites →https://doi.org/10.2307/2418649openalex-snapshot
A New Tabular and Diagrammatic Method for Displaying Artificial Hybridization Data, with an Example from Aphelandra (Acanthaceae)
inferredcites →https://doi.org/10.2307/2418921openalex-snapshot
Patterns of Crossability and Interfertility in Subtribe Maurandyinae (Scrophulariaceae-Antirrhineae)
inferredcites →https://doi.org/10.2307/2419349openalex-snapshot
The Evolution of Self-Pollination in Granite Outcrop Species of Arenaria (Caryophyllaceae) V. Artificial Crosses Within and Between Populations
inferredcites →https://doi.org/10.2307/2419350openalex-snapshot
Cytogenetics and Hybridization of Portulaca in Hawaii
inferredcites →https://doi.org/10.2307/2419813openalex-snapshot
Species Concepts and Problems in Practice: Insight from Botanical Monographs
inferredcites →https://doi.org/10.2307/2446534openalex-snapshot
Artificial hybridization in the Hawaiian endemic genus Labordia (Loganiaceae)
inferredcites →https://doi.org/10.2307/2656739openalex-snapshot
Inbreeding, outbreeding, and heterosis in the yellow pitcher plant, Sarracenia flava (Sarraceniaceae), in Virginia
inferredcites →https://doi.org/10.2307/2657086openalex-snapshot
Cross‐fertility in two tropical tree species: evidence of inbreeding depression within populations and genetic divergence among populations
inferredcites →https://doi.org/10.2307/3558414openalex-snapshot
Assessment of hybridization and introgression in lava‐colonizing Hawaiian Dubautia (Asteraceae: Madiinae) using RAPD markers
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
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.110.1.2zenodo-depositor-declared
A revision of loasoid Caiophora (Caiophora pterosperma-group, Loasoideae, Loasaceae) from Peru
inferred← citeshttps://doi.org/10.11646/phytotaxa.202.4.2zenodo-depositor-declared
Notes on Malesherbia (Passifloraceae) in Peru: a new species from southern Peru, a new record and a first report on interspecific hybridization in Malesherbia
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/10.1007/s00606-012-0646-0openalex-snapshot
Interspecific and intergeneric hybridization in South American Rhamnaceae-Colletieae
inferred← citeshttps://doi.org/10.1007/s12229-013-9125-8openalex-snapshot
Molecular Markers and Conservation of Plant Species in the Latin-America: The Case of Phaedranassa viridiflora (Amaryllidaceae)
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/10.1093/aob/mcw035openalex-snapshot
Exploring the ontogenetic scaling hypothesis during the diversification of pollination syndromes inCaiophora(Loasaceae, subfam. Loasoideae)
inferred← citeshttps://doi.org/10.1093/aobpla/plw034openalex-snapshot
Genetic admixture and lineage separation in a southern Andean plant
inferred← citeshttps://doi.org/10.1093/botlinnean/boab070openalex-snapshot
Hybridisation: A ‘double-edged sword’ for neotropical plant diversity
inferred← citeshttps://doi.org/10.1093/sysbio/syr084openalex-snapshot
Species Delimitation: Inferring Gaps in Morphology across Geography
inferred← citeshttps://doi.org/10.1111/boj.12447openalex-snapshot
Maintenance of species integrity in the context of a recent radiation: the case ofJamesbrittenia(Scrophulariaceae: Limoselleae) in southern Africa
inferred← citeshttps://doi.org/10.1111/jse.12726openalex-snapshot
Integrative taxonomy of herbaceous plants with narrow fragmented distributions: A case study on Primula merrilliana species complex
inferred← citeshttps://doi.org/10.1111/plb.70189openalex-snapshot
Heterosis and hybrid breakdown in the Dimorphandra hybrid zone in a savanna/forest ecotone
inferred← citeshttps://doi.org/10.14522/darwiniana.2022.101.1031openalex-snapshot
Caiophora vallegrandensis (Loasaceae, Loasoideae, Loaseae): Una nueva especie de Argentina
inferred← citeshttps://doi.org/10.3417/d-16-00013openalex-snapshot
New Species ofCalceolaria(Calceolariaceae) from Northern Peru
inferred← citeshttps://doi.org/10.3732/ajb.0900165openalex-snapshot
New insights into the phylogenetic relationships, character evolution, and phytogeographic patterns of Calceolaria (Calceolariaceae)
inferred← citeshttps://doi.org/10.64898/2026.05.28.728564openalex-snapshot
Divergent habitat selection across many loci maintains species boundaries during introgression
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