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Relationships between environmental gradients and geographic variation in the intraspecific body size of three species of frogs (Anura)

https://doi.org/10.1111/aec.12267
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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/joc.1276openalex-snapshot
Very high resolution interpolated climate surfaces for global land areas
inferredcites →https://doi.org/10.1007/978-1-4757-2917-7openalex-snapshot
Model Selection and Inference
inferredcites →https://doi.org/10.1007/bf00649503openalex-snapshot
Latitudinal patterns in European ant assemblages: variation in species richness and body size
inferredcites →https://doi.org/10.1007/s00442-014-3147-8openalex-snapshot
Andrew meets Rensch: sexual size dimorphism and the inverse of Rensch’s rule in Andrew’s toad (Bufo andrewsi)
inferredcites →https://doi.org/10.1007/s10531-008-9434-0openalex-snapshot
Diversity of reproductive modes in anurans communities in the Caatinga (dryland) of northeastern Brazil
inferredcites →https://doi.org/10.1007/s10682-011-9501-yopenalex-snapshot
Adult body size = f (initial size + growth rate × age): explaining the proximate cause of Bergman’s cline in a toad along altitudinal gradients
inferredcites →https://doi.org/10.1016/0010-406x(69)91342-5openalex-snapshot
Studies on anuran water balance—I. Dynamics of evaporative water loss by the coquí, eleutherodactylus portoricensis
inferredcites →https://doi.org/10.1016/0306-4565(94)00028-hopenalex-snapshot
Effects of temperature on the size of aquatic ectotherms: Exceptions to the general rule
inferredcites →https://doi.org/10.1016/j.ics.2004.08.061openalex-snapshot
A preliminary assessment of anuran physiological and morphological adaptation to the Caatinga, a Brazilian semi-arid environment
inferredcites →https://doi.org/10.1016/s0065-2504(08)60212-3openalex-snapshot
Temperature and Organism Size—A Biological Law for Ectotherms?
inferredcites →https://doi.org/10.1016/s0169-5347(97)01058-6openalex-snapshot
Why are organisms usually bigger in colder environments? Making sense of a life history puzzle
inferredcites →https://doi.org/10.1046/j.1365-2656.2003.00696.xopenalex-snapshot
Geographic variation in life‐history characteristics of amphibians: a review
inferredcites →https://doi.org/10.1046/j.1472-4642.1999.00046.xopenalex-snapshot
Geographic gradients in body size: a clarification of Bergmann's rule
inferredcites →https://doi.org/10.1046/j.1523-1739.1994.08010060.xopenalex-snapshot
Amphibian Declines: Judging Stability, Persistence, and Susceptibility of Populations to Local and Global Extinctions
inferredcites →https://doi.org/10.1086/303400openalex-snapshot
Is Bergmann’s Rule Valid for Mammals?
inferredcites →https://doi.org/10.1086/377187openalex-snapshot
The Temperature‐Size Rule in Ectotherms: Simple Evolutionary Explanations May Not Be General
inferredcites →https://doi.org/10.1093/icb/23.1.85openalex-snapshot
Interpreting Geographic Variation in Life-History Traits
inferredcites →https://doi.org/10.1093/icb/44.6.498openalex-snapshot
Temperature, Growth Rate, and Body Size in Ectotherms: Fitting Pieces of a Life-History Puzzle
inferredcites →https://doi.org/10.1111/bij.12018openalex-snapshot
Environmental steepness, tolerance gradient, and ecogeographical rules in glassfrogs (Anura: Centrolenidae)
inferredcites →https://doi.org/10.1111/j.0014-3820.2003.tb00324.xopenalex-snapshot
BERGMANN'S RULE IN NONAVIAN REPTILES: TURTLES FOLLOW IT, LIZARDS AND SNAKES REVERSE IT
inferredcites →https://doi.org/10.1111/j.1095-8312.1938.tb00182k.xopenalex-snapshot
SOME PROBLEMS OF GEOGRAPHICAL VARIATION AND SPECIES-FORMATION.
inferredcites →https://doi.org/10.1111/j.1095-8312.2004.00315.xopenalex-snapshot
Variation in body size and sexual dimorphism across geographical and environmental space in the frogs Limnodynastes tasmaniensis and L. peronii
inferredcites →https://doi.org/10.1111/j.1365-2699.2006.01435.xopenalex-snapshot
Broad‐scale patterns of body size in squamate reptiles of Europe and North America
inferredcites →https://doi.org/10.1111/j.1365-2699.2007.01708.xopenalex-snapshot
Subterranean rodents of the genusCtenomys(Caviomorpha, Ctenomyidae) follow the converse to Bergmann's rule
inferredcites →https://doi.org/10.1111/j.1365-2699.2007.01772.xopenalex-snapshot
Ecogeographical rules: elements of a synthesis
inferredcites →https://doi.org/10.1111/j.1365-2699.2009.02163.xopenalex-snapshot
Climate history, human impacts and global body size of Carnivora (Mammalia: Eutheria) at multiple evolutionary scales
inferredcites →https://doi.org/10.1111/j.1439-0469.2008.00504.xopenalex-snapshot
Bergmann’s rule in amphibians: combining demographic and ecological parameters to explain body size variation among populations in the common toadBufo bufo
inferredcites →https://doi.org/10.1111/j.1466-8238.2007.00309.xopenalex-snapshot
Energy and interspecific body size patterns of amphibian faunas in Europe and North America: anurans follow Bergmann's rule, urodeles its converse
inferredcites →https://doi.org/10.1111/j.1466-8238.2007.00343.xopenalex-snapshot
The geography of body size – challenges of the interspecific approach
inferredcites →https://doi.org/10.1111/j.1466-8238.2007.00363.xopenalex-snapshot
Bergmann's rule and the geography of mammal body size in the Western Hemisphere
inferredcites →https://doi.org/10.1111/j.1466-8238.2010.00577.xopenalex-snapshot
Bergmann's Rule – what's in a name?
inferredcites →https://doi.org/10.1111/j.1469-185x.2009.00097.xopenalex-snapshot
Body size variation in insects: a macroecological perspective
inferredcites →https://doi.org/10.1111/j.1558-5646.1956.tb02836.xopenalex-snapshot
GEOGRAPHICAL CHARACTER GRADIENTS AND CLIMATIC ADAPTATION
inferredcites →https://doi.org/10.1111/j.1558-5646.1979.tb04714.xopenalex-snapshot
COUNTERGRADIENT SELECTION IN THE GREEN FROG, RANA CLAMITANS
inferredcites →https://doi.org/10.1111/j.1558-5646.1997.tb02453.xopenalex-snapshot
ECTOTHERMS FOLLOW THE CONVERSE TO BERGMANN'S RULE
inferredcites →https://doi.org/10.1111/j.1558-5646.2007.00297.xopenalex-snapshot
AMPHIBIANS DO NOT FOLLOW BERGMANN'S RULE
inferredcites →https://doi.org/10.1111/j.1600-0587.2008.05632.xopenalex-snapshot
Geographic body size gradients in tropical regions: water deficit and anuran body size in the Brazilian Cerrado
inferredcites →https://doi.org/10.1111/j.1600-0587.2010.06244.xopenalex-snapshot
Cross‐species and assemblage‐based approaches to Bergmann's rule and the biogeography of body size in Plethodon salamanders of eastern North America
inferredcites →https://doi.org/10.1111/j.1600-0706.2009.17959.xopenalex-snapshot
Bergmann's rule; a concept cluster?
inferredcites →https://doi.org/10.1111/j.1600-0706.2011.19319.xopenalex-snapshot
“Nullius in Bergmann” or the pluralistic approach to ecogeographical rules: a reply to Watt et al. (2010)
inferredcites →https://doi.org/10.1111/j.2007.0906-7590.05171.xopenalex-snapshot
Methods to account for spatial autocorrelation in the analysis of species distributional data: a review
inferredcites →https://doi.org/10.1139/z02-049openalex-snapshot
Do amphibians follow Bergmann's rule?
inferredcites →https://doi.org/10.1139/z06-180openalex-snapshot
Comparative demography of a temperate anuran, Rana chensinensis, along a relatively fine elevational gradient
inferredcites →https://doi.org/10.1146/annurev.es.11.110180.000435openalex-snapshot
Complex Life Cycles
inferredcites →https://doi.org/10.1163/156853888x00206openalex-snapshot
Vocalizations and reproductive behaviour in the smith frog, Hyla faber Wied (Amphibia: Hylidae)
inferredcites →https://doi.org/10.1641/0006-3568(2005)055[0207:rmifat]2.0.co;2openalex-snapshot
Reproductive Modes in Frogs and Their Unexpected Diversity in the Atlantic Forest of Brazil
inferredcites →https://doi.org/10.1670/09-202.1openalex-snapshot
Inter- and Intraspecific Geographic Variation of Body Size in South American Redbelly Toads of the Genus Melanophryniscus Gallardo, 1961 (Anura: Bufonidae)
inferredcites →https://doi.org/10.2307/1934189openalex-snapshot
Adaptive Variation in Size of Cricket Frogs
inferredcites →https://doi.org/10.2307/1935374openalex-snapshot
Geographic Size Variation in Birds and Its Relationship to Climate
inferredcites →https://doi.org/10.2307/1942232openalex-snapshot
Role of Temperature and Water in the Ecology of Lungless Salamanders
inferredcites →https://doi.org/10.2307/3802723openalex-snapshot
Model Selection and Multimodel Inference: A Practical Information-Theoretic Approach
inferredcites →https://doi.org/10.32614/r.manualsopenalex-snapshot
R: A Language and Environment for Statistical Computing
inferredcites →https://doi.org/10.56021/9780801847806openalex-snapshot
Biology of Amphibians

What points at this work

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

inferred← citeshttps://doi.org/10.3897/herpetozoa.37.e108976zenodo-depositor-declared
Diet, sexual dimorphism, and fertility aspects of Melanophryniscus fulvoguttatus (Mertens, 1937) from Central-East Brazil
inferred← citeshttps://doi.org/10.1002/ece3.4007openalex-snapshot
Geographic variation in body size and its relationship with environmental gradients in the Oriental Garden Lizard, Calotes versicolor
inferred← citeshttps://doi.org/10.1002/ece3.73298openalex-snapshot
Spatial Structure Explains Morphological Variation Better Than Climatic Gradients in the South American Rattlesnake ( Crotalus durissus )
inferred← citeshttps://doi.org/10.1007/978-1-4939-8919-5_8openalex-snapshot
Multidimensional Analyses for Testing Ecological, Ethnobiological, and Conservation Hypotheses
inferred← citeshttps://doi.org/10.1007/s00027-023-00943-1openalex-snapshot
Living in a changing world: effects of roads and Pinus monocultures on an anuran metacommunity in southern Brazil
inferred← citeshttps://doi.org/10.1007/s10682-025-10352-5openalex-snapshot
Geographic variation of body size in a plateau anuran: evidence supporting the water availability and heat balance trade-off hypothesis
inferred← citeshttps://doi.org/10.1080/02724634.2026.2689465openalex-snapshot
A new extinct Pleistocene species of spadefoot toad and comments on the paleoecology and paleobiogeography of anurans from Rancho La Brea, California
inferred← citeshttps://doi.org/10.1086/700833openalex-snapshot
Biophysical Modeling of Water Economy Can Explain Geographic Gradient of Body Size in Anurans
inferred← citeshttps://doi.org/10.1093/zoolinnean/zlaf183openalex-snapshot
Integrating allometry for accurate identification of Anura fossils from the Naracoorte Caves World Heritage Area
inferred← citeshttps://doi.org/10.1111/aec.12532openalex-snapshot
Body size variation and sexual size dimorphism across climatic gradients in the widespread treefrog Scinax fuscovarius (Anura, Hylidae)
inferred← citeshttps://doi.org/10.1111/gcb.15997openalex-snapshot
Survival of climate warming through niche shifts: Evidence from frogs on tropical islands
inferred← citeshttps://doi.org/10.1111/jbi.12842openalex-snapshot
Geographical clines of body size in terrestrial amphibians: water conservation hypothesis revisited
inferred← citeshttps://doi.org/10.1111/jbi.15095openalex-snapshot
Temperature and Moisture Interact to Shape Body Size of Appalachian Salamanders Across Elevation
inferred← citeshttps://doi.org/10.1111/jzo.12787openalex-snapshot
Seasonality drives body size variation in a widely distributed Neotropical treefrog
inferred← citeshttps://doi.org/10.1111/mec.16035openalex-snapshot
Phenotypic and genomic diversification with isolation by environment along elevational gradients in a neotropical treefrog
inferred← citeshttps://doi.org/10.1186/s40850-021-00090-wopenalex-snapshot
The Atacama toad (Rhinella atacamensis) exhibits an unusual clinal pattern of decreasing body size towards more arid environments
inferred← citeshttps://doi.org/10.13047/kjee.2018.32.6.575openalex-snapshot
Relationship between Body Size Variation and Habitat Environment of Hyla japonica in Jeju Island, South Korea
inferred← citeshttps://doi.org/10.1371/journal.pone.0191691openalex-snapshot
The advertisement calls of Brazilian anurans: Historical review, current knowledge and future directions
inferred← citeshttps://doi.org/10.1655/herpetologica-d-19-00046.1openalex-snapshot
Geographic Variation in the Acoustic Signals of Dendropsophus nanus (Boulenger 1889) (Anura: Hylidae)
inferred← citeshttps://doi.org/10.22541/au.159645990.05594317openalex-snapshot
Environmental variation predicts patterns of phenotypic and genomic variation in an African tropical forest frog
inferred← citeshttps://doi.org/10.3390/biology11121766openalex-snapshot
Geographical Variation in Body Size and the Bergmann’s Rule in Andrew’s Toad (Bufo andrewsi)
inferred← citeshttps://doi.org/10.3390/insects15020125openalex-snapshot
Demography and Behaviour of Teinopodagrion oscillans (Odonata: Megapodagrionidae) in a Protected Area of the Colombian Andean Region
inferred← citeshttps://doi.org/10.35537/10915/60932openalex-snapshot
Efectos de la degradación del hábitat sobre la composición del ensamble de anuros del Bosque Atlántico en Misiones (Argentina)
inferred← citeshttps://doi.org/10.52050/9788579175633openalex-snapshot
Análises ecológicas no R
inferred← citeshttps://doi.org/10.6084/m9.figshare.16584339openalex-snapshot
Additional file 1 of The Atacama toad (Rhinella atacamensis) exhibits an unusual clinal pattern of decreasing body size towards more arid environments
inferred← citeshttps://doi.org/10.6084/m9.figshare.16584342openalex-snapshot
Additional file 2 of The Atacama toad (Rhinella atacamensis) exhibits an unusual clinal pattern of decreasing body size towards more arid environments
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