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Distribution and habitat segregation on different spatial scales among diploid, tetraploid and hexaploid cytotypes of Senecio carniolicus (Asteraceae) in the Eastern Alps

https://doi.org/10.1093/aob/mcq192
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What this work says

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

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inferredcites →https://doi.org/10.1007/bf00385262openalex-snapshot
Polyploidy and habitat differentiation in Dactylis glomerata L. from Galicia (Spain)
inferredcites →https://doi.org/10.1007/bf00419154openalex-snapshot
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inferredcites →https://doi.org/10.1007/s10265-007-0108-xopenalex-snapshot
Sympatric diploid and hexaploid cytotypes of Senecio carniolicus (Asteraceae) in the Eastern Alps are separated along an altitudinal gradient
inferredcites →https://doi.org/10.1007/s10682-007-9228-yopenalex-snapshot
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inferredcites →https://doi.org/10.1111/j.1365-2656.2007.01300.xopenalex-snapshot
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inferredcites →https://doi.org/10.1111/j.1365-2699.2004.01065.xopenalex-snapshot
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inferredcites →https://doi.org/10.1111/j.1365-294x.2005.02683.xopenalex-snapshot
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inferredcites →https://doi.org/10.2307/3647447openalex-snapshot
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inferredcites →https://doi.org/10.32614/r.manualsopenalex-snapshot
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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.213.1.1zenodo-depositor-declared
Underestimated diversity in one of the world’s best studied mountain ranges: The polyploid complex of Senecio carniolicus (Asteraceae) contains four species in the European Alps
inferred← citeshttps://doi.org/10.3897/phytokeys.267.162132zenodo-depositor-declared
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inferred← citeshttps://doi.org/10.1002/ajb2.1431openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ajb2.1534openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ajb2.16077openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ece3.1430openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ece3.3684openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ece3.7791openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-3-7091-1160-4_16openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00035-011-0091-7openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00035-018-0209-2openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00035-021-00254-xopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00035-025-00331-5openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00606-011-0530-3openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00606-014-1163-0openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00606-019-01621-2openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10577-011-9232-5openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11056-021-09901-xopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s12224-012-9126-0openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.ppees.2015.02.001openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.sajb.2013.05.005openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tplants.2017.09.011openalex-snapshot
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inferred← citeshttps://doi.org/10.1086/691460openalex-snapshot
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inferred← citeshttps://doi.org/10.1093/aob/mcab123openalex-snapshot
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inferred← citeshttps://doi.org/10.1093/aob/mcae096openalex-snapshot
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inferred← citeshttps://doi.org/10.1093/aob/mcr277openalex-snapshot
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inferred← citeshttps://doi.org/10.1093/aob/mcs171openalex-snapshot
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inferred← citeshttps://doi.org/10.1093/aob/mct030openalex-snapshot
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inferred← citeshttps://doi.org/10.1093/aob/mct074openalex-snapshot
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inferred← citeshttps://doi.org/10.1093/aob/mcv176openalex-snapshot
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inferred← citeshttps://doi.org/10.1093/aob/mcx032openalex-snapshot
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inferred← citeshttps://doi.org/10.1093/aob/mcz070openalex-snapshot
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inferred← citeshttps://doi.org/10.1093/aobpla/plab015openalex-snapshot
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inferred← citeshttps://doi.org/10.1093/aobpla/plac052openalex-snapshot
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inferred← citeshttps://doi.org/10.1093/aobpla/plz028openalex-snapshot
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inferred← citeshttps://doi.org/10.1093/biolinnean/bly065openalex-snapshot
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inferred← citeshttps://doi.org/10.1093/botlinnean/bow009openalex-snapshot
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inferred← citeshttps://doi.org/10.1093/jpe/rtw039openalex-snapshot
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inferred← citeshttps://doi.org/10.1098/rspb.2022.2456openalex-snapshot
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inferred← citeshttps://doi.org/10.1098/rstb.2013.0352openalex-snapshot
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inferred← citeshttps://doi.org/10.1101/2023.02.23.529645openalex-snapshot
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inferred← citeshttps://doi.org/10.1111/1755-0998.12641openalex-snapshot
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inferred← citeshttps://doi.org/10.1111/boj.12190openalex-snapshot
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inferred← citeshttps://doi.org/10.1111/boj.12214openalex-snapshot
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inferred← citeshttps://doi.org/10.1111/boj.12232openalex-snapshot
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inferred← citeshttps://doi.org/10.1111/boj.12306openalex-snapshot
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inferred← citeshttps://doi.org/10.1111/evo.14077openalex-snapshot
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inferred← citeshttps://doi.org/10.1111/jbi.12663openalex-snapshot
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inferred← citeshttps://doi.org/10.1111/jbi.13629openalex-snapshot
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inferred← citeshttps://doi.org/10.1111/jbi.14133openalex-snapshot
Impact of Quaternary climatic oscillations on phylogeographic patterns of three habitat‐segregated Cerastium taxa endemic to the Dinaric Alps
inferred← citeshttps://doi.org/10.1111/jbi.14627openalex-snapshot
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inferred← citeshttps://doi.org/10.1111/jse.12471openalex-snapshot
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inferred← citeshttps://doi.org/10.1111/nph.15426openalex-snapshot
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inferred← citeshttps://doi.org/10.1111/rec.12408openalex-snapshot
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inferred← citeshttps://doi.org/10.1159/000351727openalex-snapshot
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inferred← citeshttps://doi.org/10.1186/s12862-015-0425-yopenalex-snapshot
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inferred← citeshttps://doi.org/10.1186/s12862-016-0773-2openalex-snapshot
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inferred← citeshttps://doi.org/10.12705/624.8openalex-snapshot
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inferred← citeshttps://doi.org/10.12705/676.9openalex-snapshot
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inferred← citeshttps://doi.org/10.1371/journal.pone.0078959openalex-snapshot
Parental Ploidy Strongly Affects Offspring Fitness in Heteroploid Crosses among Three Cytotypes of Autopolyploid Jacobaea carniolica (Asteraceae)
inferred← citeshttps://doi.org/10.1371/journal.pone.0086247openalex-snapshot
DNA Content Variation and Its Significance in the Evolution of the Genus Micrasterias (Desmidiales, Streptophyta)
inferred← citeshttps://doi.org/10.1371/journal.pone.0118197openalex-snapshot
Polyploidisation and Geographic Differentiation Drive Diversification in a European High Mountain Plant Group (Doronicum clusii Aggregate, Asteraceae)
inferred← citeshttps://doi.org/10.1371/journal.pone.0218389openalex-snapshot
Polyploid evolution: The ultimate way to grasp the nettle
inferred← citeshttps://doi.org/10.23855/preslia.2019.143openalex-snapshot
Genetically divergent cytotypes of Vaccinium uliginosum co-occurring in the central Eastern Alps can be distinguished based on the morphology of their flowers
inferred← citeshttps://doi.org/10.23855/preslia.2021.305openalex-snapshot
Whole genome duplication increases ecological niche breadth of the perennial herb Urtica dioica
inferred← citeshttps://doi.org/10.2985/026.029.0111openalex-snapshot
Cytogenetic Characteristics of Four Gymnocalycium (Cactaceae) Species along Altitudinal Gradients
inferred← citeshttps://doi.org/10.3389/fgene.2018.00639openalex-snapshot
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inferred← citeshttps://doi.org/10.3389/fpls.2016.01329openalex-snapshot
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inferred← citeshttps://doi.org/10.3389/fpls.2020.00315openalex-snapshot
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inferred← citeshttps://doi.org/10.3389/fpls.2020.591137openalex-snapshot
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inferred← citeshttps://doi.org/10.3389/fpls.2021.589093openalex-snapshot
Eunuchs or Females? Causes and Consequences of Gynodioecy on Morphology, Ploidy, and Ecology of Stellaria graminea L. (Caryophyllaceae)
inferred← citeshttps://doi.org/10.3389/fpls.2022.873471openalex-snapshot
Genetic Variability in Balkan Paleoendemic Resurrection Plants Ramonda serbica and R. nathaliae Across Their Range and in the Zone of Sympatry
inferred← citeshttps://doi.org/10.3390/plants11111481openalex-snapshot
Genome Size Variation in Dianthus sylvestris Wulfen sensu lato (Caryophyllaceae)
inferred← citeshttps://doi.org/10.3390/plants12040973openalex-snapshot
Disentangling Relationships among the Alpine Species of Luzula Sect. Luzula (Juncaceae) in the Eastern Alps
inferred← citeshttps://doi.org/10.3398/064.071.0201openalex-snapshot
Natural Polyploidization within Tetraploid and Hexaploid Populations of the Desert ShrubAtriplex confertifolia
inferred← citeshttps://doi.org/10.3732/ajb.1100018openalex-snapshot
Differences in spatial distribution, morphology, and communities of herbivorous insects among three cytotypes of Solidago altissima (Asteraceae)
inferred← citeshttps://doi.org/10.3732/ajb.1400005openalex-snapshot
Nonadaptive processes governing early stages of polyploid evolution: Insights from a primary contact zone of relict serpentine Knautia arvensis (Caprifoliaceae)
inferred← citeshttps://doi.org/10.3732/ajb.1400296openalex-snapshot
Environmental correlates of cytotype distribution in Andropogon gerardii (Poaceae)
inferred← citeshttps://doi.org/10.3732/ajb.1500052openalex-snapshot
Cytotype distribution patterns, ecological differentiation, and genetic structure in a diploid–tetraploid contact zone of Cardamine amara
inferred← citeshttps://doi.org/10.3732/ajb.1600365openalex-snapshot
Cytogeography of the subalpine marsh marigold polyploid complex (Caltha leptosepala s.l., Ranunculaceae)
inferred← citeshttps://doi.org/10.4081/nhs.2015.246openalex-snapshot
Four new combinations in Jacobaea Mill. (Asteraceae, Senecioneae) for the European flora
inferred← citeshttps://doi.org/10.53846/goediss-7292openalex-snapshot
Cytotype Associations, Ecological Divergence and Genetic Variation in the Apomictic Complex Paspalum intermedium Munro Ex Morong (Poaceae)
inferred← citeshttps://doi.org/10.5735/085.056.0111openalex-snapshot
Complex Pattern of Ploidal and Genetic Variation in Seseli libanotis (Apiaceae)
inferred← citeshttps://doi.org/10.64898/2026.01.21.700804openalex-snapshot
Flow cytometry protocols, relative genome size and ploidy levels for 1104 species of non-apomictic angiosperms from the Eastern Alps – a community resource based on the screening of 45,000 samples
inferred← citeshttps://doi.org/10.7287/peerj.5209v0.1/reviews/1openalex-snapshot
Peer Review #1 of "Distribution and ecological segregation on regional and microgeographic scales of the diploid Centaurea aspera L., the tetraploid C. seridis L., and their triploid hybrids (Compositae) (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.5209v0.1/reviews/2openalex-snapshot
Peer Review #2 of "Distribution and ecological segregation on regional and microgeographic scales of the diploid Centaurea aspera L., the tetraploid C. seridis L., and their triploid hybrids (Compositae) (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.5209v0.1/reviews/3openalex-snapshot
Peer Review #3 of "Distribution and ecological segregation on regional and microgeographic scales of the diploid Centaurea aspera L., the tetraploid C. seridis L., and their triploid hybrids (Compositae) (v0.1)"
inferred← citeshttps://doi.org/10.7717/peerj.5209openalex-snapshot
Distribution and ecological segregation on regional and microgeographic scales of the diploid Centaurea aspera L., the tetraploid C. seridis L., and their triploid hybrids (Compositae)
Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.