On the public citation graph

Phenotypic plasticity in Carlina vulgaris: effects of geographical origin, population size, and population isolation

0 signed · 93 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.
Claim with ORCID
Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

What this work says

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

inferredcites →https://doi.org/10.1002/j.1537-2197.1984.tb12511.xopenalex-snapshot
PHENOTYPIC PLASTICITY OF ANNUAL PHLOX: TESTS OF SOME HYPOTHESES
inferredcites →https://doi.org/10.1002/j.1537-2197.1988.tb13428.xopenalex-snapshot
PHENOTYPIC PLASTICITY IN PHLOX. I. WILD AND CULTIVATED POPULATIONS OF P. DRUMMONDII
inferredcites →https://doi.org/10.1002/j.1537-2197.1989.tb15147.xopenalex-snapshot
POPULATION DIFFERENTIATION FOR PHENOTYPIC PLASTICITY IN THE STELLARIA LONGIPES COMPLEX
inferredcites →https://doi.org/10.1002/j.1537-2197.1995.tb11582.xopenalex-snapshot
R eaction norms of A rabidopsis ( Brassicaceae ). III. R esponse to nutrients in 26 populations from a worldwide collection
inferredcites →https://doi.org/10.1007/bf00317601openalex-snapshot
The significance of genetic erosion in the process of extinction
inferredcites →https://doi.org/10.1007/bf00378740openalex-snapshot
Phenotypic plasticity in Phlox
inferredcites →https://doi.org/10.1007/bf00941151openalex-snapshot
Phenotypic plasticity inLemna minor (Lemnaceae)
inferredcites →https://doi.org/10.1016/b978-0-12-473542-2.x5000-7openalex-snapshot
Mineral Nutrition of Higher Plants
inferredcites →https://doi.org/10.1016/s0065-2660(08)60048-6openalex-snapshot
Evolutionary Significance of Phenotypic Plasticity in Plants
inferredcites →https://doi.org/10.1016/s0367-2530(17)31500-1openalex-snapshot
Zur ökophysiologischen und ökogeographischen Differenzierung nah verwandter Carlina-Arten
inferredcites →https://doi.org/10.1023/a:1023289519129openalex-snapshot
Patch distribution and dispersal limitation of four plant species in Swedish semi-natural grasslands
inferredcites →https://doi.org/10.1023/b:coge.0000029999.10808.c2openalex-snapshot
Genetic diversity and fitness in Scabiosa columbaria in the Swiss Jura in relation to population size
inferredcites →https://doi.org/10.1038/hdy.1994.167openalex-snapshot
Reaction norm variation in a rare plant, Senecio integrifolius (Asteraceae)
inferredcites →https://doi.org/10.1038/hdy.1997.154openalex-snapshot
Reaction norm variation between and within populations of two rare plant species, Vicia pisiformis and V. dumetorum (Fabaceae)
inferredcites →https://doi.org/10.1046/j.1365-2745.1998.00246.xopenalex-snapshot
Effects of population size on performance in the rare plant Gentianella germanica
inferredcites →https://doi.org/10.1046/j.1365-2745.2000.00422.xopenalex-snapshot
Reduced fecundity and offspring performance in small populations of the declining grassland plants Primula veris and Gentiana lutea
inferredcites →https://doi.org/10.1046/j.1365-2745.2003.00785.xopenalex-snapshot
Effects of population size and genetic variation on the response of Succisa pratensis to eutrophication and acidification
inferredcites →https://doi.org/10.1046/j.1365-294x.2001.01169.xopenalex-snapshot
Genetic structure of the annual weedSenecio vulgarisin relation to habitat type and population size
inferredcites →https://doi.org/10.1046/j.1420-9101.1990.3050411.xopenalex-snapshot
Phenotypic plasticity in Phlox. III. Variation among natural populations of P. drummondii
inferredcites →https://doi.org/10.1046/j.1461-0248.2000.00188.xopenalex-snapshot
Genetic Allee effects on performance, plasticity and developmental stability in a clonal plant
inferredcites →https://doi.org/10.1046/j.1523-1739.1999.98278.xopenalex-snapshot
Genetic Diversity, Population Size, and Fitness in Central and Peripheral Populations of a Rare Plant Lychnis viscaria
inferredcites →https://doi.org/10.1046/j.1523-1739.2000.99283.xopenalex-snapshot
Population Persistence and Offspring Fitness in the Rare Bellflower Campanula cervicaria in Relation to Population Size and Habitat Quality
inferredcites →https://doi.org/10.1086/282558openalex-snapshot
Phenotypic Placticity of Avena fatua and A. barbata
inferredcites →https://doi.org/10.1086/297291openalex-snapshot
Phenotypic Plasticity and Genetic Variation of Vaccinium macrocarpon, the American Cranberry. I. Reaction Norms of Clones from Central and Marginal Populations in a Common Garden
inferredcites →https://doi.org/10.1086/368395openalex-snapshot
Adaptive Differentiation in Response to Water Stress by Edaphic Races of Lasthenia californica (Asteraceae)
inferredcites →https://doi.org/10.1093/aob/mcf164openalex-snapshot
Phenotypic Plasticity and Integration in Response to Flooded Conditions in Natural Accessions of Arabidopsis thaliana (L.) Heynh (Brassicaceae)
inferredcites →https://doi.org/10.1111/j.0014-3820.2002.tb01454.xopenalex-snapshot
EVOLUTION IN THE REAL WORLD: STOCHASTIC VARIATION AND THE DETERMINANTS OF FITNESS IN CARLINA VULGARIS
inferredcites →https://doi.org/10.1111/j.0014-3820.2003.tb01541.xopenalex-snapshot
POPULATION SIZE AND IDENTITY INFLUENCE THE REACTION NORM OF THE RARE, ENDEMIC PLANT COCHLEARIA BAVARICA ACROSS A GRADIENT OF ENVIRONMENTAL STRESS
inferredcites →https://doi.org/10.1111/j.0014-3820.2004.tb01644.xopenalex-snapshot
THE GENETIC BASIS OF ADAPTIVE POPULATION DIFFERENTIATION: A QUANTITATIVE TRAIT LOCUS ANALYSIS OF FITNESS TRAITS IN TWO WILD BARLEY POPULATIONS FROM CONTRASTING HABITATS
inferredcites →https://doi.org/10.1111/j.1365-2745.2004.00857.xopenalex-snapshot
Phenotypic plasticity of vegetative and reproductive traits in monoecious and dioecious populations of Sagittaria latifolia (Alismataceae): a clonal aquatic plant
inferredcites →https://doi.org/10.1111/j.1438-8677.1992.tb01333.xopenalex-snapshot
Meta-population dynamics of biennial plants: how to exploit temporary habitats
inferredcites →https://doi.org/10.1111/j.1438-8677.1995.tb00793.xopenalex-snapshot
Phenotypic plasticity and plant adaptation*
inferredcites →https://doi.org/10.1111/j.1469-8137.1984.tb04155.xopenalex-snapshot
ON THE ECOLOGY OF SHORT‐LIVED FORBS IN CHALK GRASSLANDS: LIFE‐HISTORY CHARACTERISTICS
inferredcites →https://doi.org/10.1111/j.1523-1739.1991.tb00120.xopenalex-snapshot
Seed Germination Percentage Increases with Population Size in a Fragmented Prairie Species
inferredcites →https://doi.org/10.1111/j.1558-5646.1993.tb02133.xopenalex-snapshot
PHENOTYPIC PLASTICITY INPOLYGONUM PERSICARIA.II. NORMS OF REACTION TO SOIL MOISTURE AND THE MAINTENANCE OF GENETIC DIVERSITY
inferredcites →https://doi.org/10.1111/j.1558-5646.1993.tb02134.xopenalex-snapshot
PHENOTYPIC PLASTICITY INPOLYGONUM PERSICARIA.III. THE EVOLUTION OF ECOLOGICAL BREADTH FOR NUTRIENT ENVIRONMENT
inferredcites →https://doi.org/10.1111/j.1600-0587.1995.tb00133.xopenalex-snapshot
Species abundance patterns of plants in Swedish semi‐natural pastures
inferredcites →https://doi.org/10.1146/annurev.es.11.110180.001313openalex-snapshot
The Mineral Nutrition of Wild Plants
inferredcites →https://doi.org/10.1146/annurev.es.17.110186.003315openalex-snapshot
THE EVOLUTION OF PHENOTYPIC PLASTICITY IN PLANTS
inferredcites →https://doi.org/10.1146/annurev.es.18.110187.001233openalex-snapshot
MATERNAL EFFECTS IN PLANTS
inferredcites →https://doi.org/10.1890/0012-9658(2001)082[0328:ppffci]2.0.co;2openalex-snapshot
PHENOTYPIC PLASTICITY FOR FITNESS COMPONENTS INPOLYGONUMSPECIES OF CONTRASTING ECOLOGICAL BREADTH
inferredcites →https://doi.org/10.2307/1219025openalex-snapshot
Illustrierte Flora von Mittel-Europa
inferredcites →https://doi.org/10.2307/1940405openalex-snapshot
Individualistic Growth Response of Tundra Plant Species to Environmental Manipulations in the Field
inferredcites →https://doi.org/10.2307/2287349openalex-snapshot
Biometry: The Principles and Practice of Statistics in Biological Research (2nd ed.).
inferredcites →https://doi.org/10.2307/2529087openalex-snapshot
Biometry. The Principles and Practice of Statistics in Biological Research
inferredcites →https://doi.org/10.2307/2656702openalex-snapshot
Dynamic phenotypic plasticity for root growth in Polygonum: a comparative study
inferredcites →https://doi.org/10.2307/2679863openalex-snapshot
Phenotypic Plasticity for Fitness Components in Polygonum Species of Contrasting Ecological Breadth
inferredcites →https://doi.org/10.2307/3236106openalex-snapshot
Changes in chalk‐grassland structure and species richness resulting from selective nutrient additions
inferredcites →https://doi.org/10.2307/3545410openalex-snapshot
The Control of Flowering in the Monocarpic Perennial Carlina vulgaris
inferredcites →https://doi.org/10.2307/3546249openalex-snapshot
An Eight-Year Study of Population Dynamics and Life-History Variation of the "Biennial" Carlina vulgaris
inferredcites →https://doi.org/10.2307/3558403openalex-snapshot
Adaptation of Senecio vulgaris (Asteraceae) to ruderal and agricultural habitats

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.11646/zootaxa.4521.4.1zenodo-depositor-declared
The oak gall wasps of Israel (Hymenoptera, Cynipidae, Cynipini)—diversity, distribution and life history
inferred← citeshttps://doi.org/10.1002/ajb2.16360openalex-snapshot
Clinal variation in quantitative traits but not in evolutionary potential along elevational and latitudinal gradients in the widespread Anthyllis vulneraria
inferred← citeshttps://doi.org/10.1002/ecy.3078openalex-snapshot
Interactive effects of large‐ and local‐scale environmental gradients on phenotypic differentiation
inferred← citeshttps://doi.org/10.1007/s00227-007-0879-6openalex-snapshot
Reproductive plasticity in mole crabs, Emerita brasiliensis, in sandy beaches with contrasting morphodynamics
inferred← citeshttps://doi.org/10.1007/s00442-006-0534-9openalex-snapshot
Local adaptation in the monocarpic perennial Carlina vulgaris at different spatial scales across Europe
inferred← citeshttps://doi.org/10.1007/s00442-010-1798-7openalex-snapshot
Differentiation and adaptation in Brassica nigra populations: interactions with related herbivores
inferred← citeshttps://doi.org/10.1007/s00606-008-0126-8openalex-snapshot
Phenological and morphological differentiation in annual Chaetanthera moenchioides (Asteraceae) over an aridity gradient
inferred← citeshttps://doi.org/10.1007/s10682-008-9285-xopenalex-snapshot
Microgeographic variation in temperature-induced plasticity in an isolated amphibian metapopulation
inferred← citeshttps://doi.org/10.1016/j.actao.2011.11.001openalex-snapshot
Region and site conditions affect phenotypic trait variation in five forest herbs
inferred← citeshttps://doi.org/10.1016/j.baae.2009.09.002openalex-snapshot
A question of origin: Where and how to collect seed for ecological restoration
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2013.09.004openalex-snapshot
Ecological and evolutionary responses of Mediterranean plants to global change
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2023.169208openalex-snapshot
Rise, fall and hope for the Sicilian endemic plant Muscari gussonei: A story of survival in the face of narrow germination optimum, climate changes, desertification and habitat fragmentation
inferred← citeshttps://doi.org/10.1017/s0960258521000234openalex-snapshot
How regional climate and seed traits interact in shaping stress–tolerance of savanna seeds?
inferred← citeshttps://doi.org/10.1093/aesa/sav053openalex-snapshot
Taxonomy and Biology ofAndricus miriami(Hymenoptera: Cynipidae: Cynipini)—A Remarkable Bud-Galling Cynipid from the Middle East
inferred← citeshttps://doi.org/10.1111/1365-2745.12372openalex-snapshot
Environmental heterogeneity leads to higher plasticity in dry‐edge populations of a semi‐arid Chilean shrub: insights into climate change responses
inferred← citeshttps://doi.org/10.1111/brv.12313openalex-snapshot
Geographic variation in genetic and demographic performance: new insights from an old biogeographical paradigm
inferred← citeshttps://doi.org/10.1111/gcb.12509openalex-snapshot
The influence of local spring temperature variance on temperature sensitivity of spring phenology
inferred← citeshttps://doi.org/10.1111/j.1095-8312.2008.01175.xopenalex-snapshot
Volatile leaf oil diversity in the narrow range endemic Eucalyptus argutifolia (Myrtaceae) and its widespread congener Eucalyptus obtusiflora
inferred← citeshttps://doi.org/10.1111/j.1365-2435.2010.01748.xopenalex-snapshot
Quantifying phenological plasticity to temperature in two temperate tree species
inferred← citeshttps://doi.org/10.1111/j.1365-2745.2006.01174.xopenalex-snapshot
Detecting local adaptation in widespread grassland species – the importance of scale and local plant community
inferred← citeshttps://doi.org/10.1111/j.1365-2745.2006.01176.xopenalex-snapshot
Quantitative estimation of phenotypic plasticity: bridging the gap between the evolutionary concept and its ecological applications
inferred← citeshttps://doi.org/10.1111/j.1365-2745.2009.01612.xopenalex-snapshot
Region versus site variation in the population dynamics of three short‐lived perennials
inferred← citeshttps://doi.org/10.1111/j.1365-2745.2011.01909.xopenalex-snapshot
Phenotypic differentiation in a common garden reflects the phylogeography of a widespread Alpine plant
inferred← citeshttps://doi.org/10.1111/j.1420-9101.2010.02138.xopenalex-snapshot
Consequences of genetic erosion on fitness and phenotypic plasticity in European tree frog populations (Hyla arborea)
inferred← citeshttps://doi.org/10.1111/j.1438-8677.2010.00342.xopenalex-snapshot
Limited phenotypic plasticity in range‐edge populations: a comparison of co‐occurring populations of two Agrimonia species with different geographical distributions
inferred← citeshttps://doi.org/10.1111/jbi.12215openalex-snapshot
Effects of marginality on plant population performance
inferred← citeshttps://doi.org/10.1111/jeb.14218openalex-snapshot
High-performing plastic clones best explain the spread of yellow monkeyflower from lowland to higher elevation areas in New Zealand
inferred← citeshttps://doi.org/10.11606/t.11.2019.tde-22032019-135219openalex-snapshot
Diversidade genética, domesticação e plasticidade fenotípica de feijão-fava (>i /i< L.)
inferred← citeshttps://doi.org/10.1590/2236-8906-01/2021openalex-snapshot
Efeitos do Tegumento e teor de água de sementes de Plathymenia reticulata e Stryphnodendron adstringens na tolerância a choques térmicos
inferred← citeshttps://doi.org/10.1890/14-1378.1openalex-snapshot
Similar plastic responses to elevated temperature among different‐sized brook trout populations
inferred← citeshttps://doi.org/10.1890/es15-00223.1openalex-snapshot
Divergent responses of leaf phenology to changing temperature among plant species and geographical regions
inferred← citeshttps://doi.org/10.26512/2014.10.t.18916openalex-snapshot
Fatores ambientais e a germinação de espécies arbóreas do Brasil Central e de áreas disjuntas da Amazônia no bioma Cerrado
inferred← citeshttps://doi.org/10.26686/wgtn.17067698openalex-snapshot
Realised Niche Shifts, Rapid Evolution and Phenotypic Plasticity in Introduced Plants
inferred← citeshttps://doi.org/10.26686/wgtn.17067698.v1openalex-snapshot
Realised Niche Shifts, Rapid Evolution and Phenotypic Plasticity in Introduced Plants
inferred← citeshttps://doi.org/10.29278/azd.476663openalex-snapshot
Phenotypic plasticity of ecotypes across habitats
inferred← citeshttps://doi.org/10.29278/azd.503049openalex-snapshot
Phenotypic plasticity of ecotypes across habitats
inferred← citeshttps://doi.org/10.3159/09-br-060.1openalex-snapshot
Noteworthy plants reported from the Torrey Range—2007 and 20081
inferred← citeshttps://doi.org/10.3389/fpls.2017.00843openalex-snapshot
Habitat Fragmentation Differentially Affects Genetic Variation, Phenotypic Plasticity and Survival in Populations of a Gypsum Endemic
inferred← citeshttps://doi.org/10.3732/ajb.0800327openalex-snapshot
Variation in flowering size and age of a facultative biennial, Aster kantoensis (Compositae), in response to nutrient availability
inferred← citeshttps://doi.org/10.3732/ajb.1100479openalex-snapshot
Effects of inbreeding and interpopulation crosses on performance and plasticity of two generations of offspring of a declining grassland plant
inferred← citeshttps://doi.org/10.5451/unibas-005676726openalex-snapshot
How glacial history and environmental variation affect population differentiation and gene flow dynamics in Alpine plant species
inferred← citeshttps://doi.org/10.70675/71fe2c9az228bz477az9710z9053891ff5beopenalex-snapshot
Variations altitudinales de traits fonctionnels foliaires chez les arbres : déterminismes environnemental et génétique
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.