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A biogeographic reversal in sexual size dimorphism along a continental temperature gradient

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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
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Thermal biology of reproduction in viviparous skinks, Eulamprus tympanum: why do gravid females bask more?
inferredcites →https://doi.org/10.1007/bf00346972openalex-snapshot
?Costs? of reproduction in reptiles
inferredcites →https://doi.org/10.1007/bf00348113openalex-snapshot
Sexual size dimorphism and male combat in snakes
inferredcites →https://doi.org/10.1007/bf00572678openalex-snapshot
Sexual size dimorphism and sexual selection in turtles (order testudines)
inferredcites →https://doi.org/10.1007/s10228-005-0286-2openalex-snapshot
Dimorphism, parasitism, and sex revisited: modes of reproduction among deep-sea ceratioid anglerfishes (Teleostei: Lophiiformes)
inferredcites →https://doi.org/10.1007/s11284-009-0607-4openalex-snapshot
A phylogenetic analysis of sex‐specific evolution of ecological morphology in Liolaemus lizards
inferredcites →https://doi.org/10.1007/s11692-011-9118-7openalex-snapshot
Fecundity Selection and the Evolution of Reproductive Output and Sex-Specific Body Size in the Liolaemus Lizard Adaptive Radiation
inferredcites →https://doi.org/10.1007/s11692-013-9232-9openalex-snapshot
An Intercontinental Analysis of Climate-Driven Body Size Clines in Reptiles: No Support for Patterns, No Signals of Processes
inferredcites →https://doi.org/10.1016/0169-5347(89)90212-7openalex-snapshot
The evolution of sexual dimorphism in animals: Hypotheses and tests
inferredcites →https://doi.org/10.1016/j.biocon.2016.03.039openalex-snapshot
Fully-sampled phylogenies of squamates reveal evolutionary patterns in threat status
inferredcites →https://doi.org/10.1016/j.tree.2014.08.003openalex-snapshot
Mistaking geography for biology: inferring processes from species distributions
inferredcites →https://doi.org/10.1016/j.ympev.2016.09.008openalex-snapshot
Lineage diversification of fringe-toed lizards (Phrynosomatidae: Uma notata complex) in the Colorado Desert: Delimiting species in the presence of gene flow
inferredcites →https://doi.org/10.1016/j.ympev.2017.04.004openalex-snapshot
Species delimitation of the blue-spotted spiny lizard within a multilocus, multispecies coalescent framework, results in the recognition of a new Sceloporus species
inferredcites →https://doi.org/10.1038/s41559-017-0332-2openalex-snapshot
The global distribution of tetrapods reveals a need for targeted reptile conservation
inferredcites →https://doi.org/10.1046/j.0021-8790.2001.00577.xopenalex-snapshot
The life‐history basis of latitudinal diversity gradients: how do species traits vary from the poles to the equator?
inferredcites →https://doi.org/10.1046/j.1365-2435.1999.00305.xopenalex-snapshot
Sexual dimorphism of head size in Gallotia galloti: testing the niche divergence hypothesis by functional analyses
inferredcites →https://doi.org/10.1086/284778openalex-snapshot
The Evolution of Large Body Size in Females: A Critique of Darwin's "Fecundity Advantage" Model
inferredcites →https://doi.org/10.1086/285144openalex-snapshot
Energy and Large-Scale Patterns of Animal- and Plant-Species Richness
inferredcites →https://doi.org/10.1086/286004openalex-snapshot
A Comparative Analysis of Allometry for Sexual Size Dimorphism: Assessing Rensch's Rule
inferredcites →https://doi.org/10.1086/416458openalex-snapshot
Ecological Causes for the Evolution of Sexual Dimorphism: A Review of the Evidence
inferredcites →https://doi.org/10.1086/520118openalex-snapshot
Geographic Variation in Body Size and Sexual Size Dimorphism of a Seed‐Feeding Beetle
inferredcites →https://doi.org/10.1086/678084openalex-snapshot
Untangling Intra- and Interspecific Effects on Body Size Clines Reveals Divergent Processes Structuring Convergent Patterns in Anolis Lizards
inferredcites →https://doi.org/10.1086/686055openalex-snapshot
Life-History Patterns of Lizards of the World
inferredcites →https://doi.org/10.1086/687575openalex-snapshot
Macroecology of Sexual Selection: A Predictive Conceptual Framework for Large-Scale Variation in Reproductive Traits
inferredcites →https://doi.org/10.1093/acprof:oso/9780199208784.003.0001openalex-snapshot
Introduction: the enigma of sexual size dimorphism
inferredcites →https://doi.org/10.1093/acprof:oso/9780199208784.003.0005openalex-snapshot
The evolution of sexual size dimorphism in reptiles
inferredcites →https://doi.org/10.1093/bioinformatics/btm538openalex-snapshot
GEIGER: investigating evolutionary radiations
inferredcites →https://doi.org/10.1093/icb/44.6.433openalex-snapshot
Body Size Clines in Sceloporus Lizards: Proximate Mechanisms and Demographic Constraints
inferredcites →https://doi.org/10.1098/rspb.2014.2213openalex-snapshot
Independent evolution of the sexes promotes amphibian diversification
inferredcites →https://doi.org/10.1111/1365-2435.12353openalex-snapshot
Sex‐specific differences in ecomorphological relationships in lizards of the genus G allotia
inferredcites →https://doi.org/10.1111/1365-2656.12248openalex-snapshot
The number of competitor species is unlinked to sexual dimorphism
inferredcites →https://doi.org/10.1111/bij.12147openalex-snapshot
Sexual dimorphism of heads and abdomens: Different approaches to ‘being large’ in female and male lizards
inferredcites →https://doi.org/10.1111/brv.12232openalex-snapshot
Fecundity selection theory: concepts and evidence
inferredcites →https://doi.org/10.1111/ecog.01531openalex-snapshot
Global geographic patterns of sexual size dimorphism in birds: support for a latitudinal trend?
inferredcites →https://doi.org/10.1111/ecog.01696openalex-snapshot
Sex‐specific responses of phenotypic diversity to environmental variation
inferredcites →https://doi.org/10.1111/ecog.02880openalex-snapshot
ENVIREM: an expanded set of bioclimatic and topographic variables increases flexibility and improves performance of ecological niche modeling
inferredcites →https://doi.org/10.1111/geb.12052openalex-snapshot
The evolution of viviparity opens opportunities for lizard radiation but drives it into a climatic cul‐de‐sac
inferredcites →https://doi.org/10.1111/geb.12053openalex-snapshot
Are lizards feeling the heat? A tale of ecology and evolution under two temperatures
inferredcites →https://doi.org/10.1111/geb.12398openalex-snapshot
Body sizes and diversification rates of lizards, snakes, amphisbaenians and the tuatara
inferredcites →https://doi.org/10.1111/geb.12722openalex-snapshot
Sexes and species as rival units of niche saturation during community assembly
inferredcites →https://doi.org/10.1111/geb.12773openalex-snapshot
Traits of lizards of the world: Variation around a successful evolutionary design
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.0014-3820.2003.tb00371.xopenalex-snapshot
A COMPARATIVE TEST OF ADAPTIVE HYPOTHESES FOR SEXUAL SIZE DIMORPHISM IN LIZARDS
inferredcites →https://doi.org/10.1111/j.1095-8312.2001.tb01298.xopenalex-snapshot
Clinal variation in body size and sexual dimorphism in an Indian fruit bat, Cynopterus sphinx (Chiroptera: Pteropodidae)
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.1420-9101.2005.00936.xopenalex-snapshot
The importance of phylogenetic scale in tests of Bergmann's and Rapoport's rules: lessons from a clade of South American lizards
inferredcites →https://doi.org/10.1111/j.1461-0248.2005.00791.xopenalex-snapshot
Ecological and community‐wide character displacement: the next generation
inferredcites →https://doi.org/10.1111/j.1466-822x.2005.00189.xopenalex-snapshot
Species turnover on elevational gradients in small rodents
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.1466-8238.2008.00414.xopenalex-snapshot
Evolution and ecology of lizard body sizes
inferredcites →https://doi.org/10.1111/j.1466-8238.2011.00700.xopenalex-snapshot
The ecology of lizard reproductive output
inferredcites →https://doi.org/10.1111/j.1558-5646.1984.tb00327.xopenalex-snapshot
ECOLOGICAL CAUSES OF SEXUAL DIMORPHISM
inferredcites →https://doi.org/10.1111/j.2041-210x.2011.00169.xopenalex-snapshot
phytools: an R package for phylogenetic comparative biology (and other things)
inferredcites →https://doi.org/10.1111/jbi.12953openalex-snapshot
Structural bias in aggregated species‐level variables driven by repeated species co‐occurrences: a pervasive problem in community and assemblage data
inferredcites →https://doi.org/10.1111/jbi.13067openalex-snapshot
The fast‐slow life‐history continuum in insular lizards: a comparison between species with invariant and variable clutch sizes
inferredcites →https://doi.org/10.11646/zootaxa.3790.3.3openalex-snapshot
A new species of bunchgrass lizard (Squamata: Phrynosomatidae) from the southern sky islands of the Sierra Madre Occidental, Mexico
inferredcites →https://doi.org/10.11646/zootaxa.3915.1.5openalex-snapshot
Anolis marsupialis Taylor 1956, a valid species from southern Pacific Costa Rica (Reptilia, Squamata, Dactyloidae)
inferredcites →https://doi.org/10.11646/zootaxa.4015.1.1openalex-snapshot
A taxonomic revision of the Phrynosoma douglasii species complex (Squamata: Phrynosomatidae)
inferredcites →https://doi.org/10.1525/california/9780520234017.001.0001openalex-snapshot
LizardsWindows to the Evolution of Diversity
inferredcites →https://doi.org/10.1554/0014-3820(2000)054[0259:trbssd]2.0.co;2openalex-snapshot
THE RELATIONSHIP BETWEEN SEXUAL SIZE DIMORPHISM AND HABITAT USE IN GREATER ANTILLEAN ANOLIS LIZARDS
inferredcites →https://doi.org/10.1554/06-110.1openalex-snapshot
WHEN RENSCH MEETS BERGMANN: DOES SEXUAL SIZE DIMORPHISM CHANGE SYSTEMATICALLY WITH LATITUDE?
inferredcites →https://doi.org/10.1670/14-162openalex-snapshot
A New Species ofAbronia(Squamata: Anguidae) from the Sierra Madre del Sur of Oaxaca, Mexico
inferredcites →https://doi.org/10.1670/15-024openalex-snapshot
A New Species ofMesaspis(Squamata: Anguidae) from the High Cuchumatanes of Guatemala
inferredcites →https://doi.org/10.2307/1445187openalex-snapshot
The Anolis Dewlap: Interspecific Variability and Morphological Associations with Habitat
inferredcites →https://doi.org/10.2307/1445294openalex-snapshot
Reproductive Influences on the Thermoregulatory Behavior of a Live-Bearing Lizard
inferredcites →https://doi.org/10.2307/1446982openalex-snapshot
Sexual Size Dimorphism in Snakes Revisited
inferredcites →https://doi.org/10.3897/zookeys.619.9650openalex-snapshot
Resurrection of Anolis ustus Cope, 1864 from synonymy with Anolis sericeus Hallowell, 1856 (Squamata, Dactyloidae)
inferredcites →https://doi.org/10.4159/harvard.9780674183384.c11openalex-snapshot
9. SEXUAL SELECTION, SEXUAL DIMORPHISM, AND TERRITORIALITY
inferredcites →https://doi.org/10.5281/zenodo.16829840openalex-snapshot
Description of two new species similar to Anolis insignis (Squamata: Iguanidae) and resurrection of Anolis (Diaphoranolis) brooksi
inferredcites →https://doi.org/10.5860/choice.47-2001openalex-snapshot
Lizards in an evolutionary tree: ecology and adaptive radiation of anoles
inferredcites →https://doi.org/10.5962/bhl.title.16228openalex-snapshot
Sexual size differences in reptiles

What points at this work

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

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New species of Paktongius and convergent evolution of the gonyleptoid-like habitus in Southeast Asian Assamiidae (Opiliones: Laniatores)
inferred← citeshttps://doi.org/10.1002/1438-390x.70012openalex-snapshot
Shorter Recruitment Periods and Higher Fecundity in High‐Latitude Populations of the Oryzias latipes Species Complex
inferred← citeshttps://doi.org/10.1002/ece3.10211openalex-snapshot
A practical guide to collections‐based research on ecogeographic rules
inferred← citeshttps://doi.org/10.1002/ece3.10393openalex-snapshot
RETRACTED: Female lizards (Eremias argus) reverse Bergmann's rule across altitude
inferred← citeshttps://doi.org/10.1002/ece3.7784openalex-snapshot
Spatial patterns in the size of Chinese lizards are driven by multiple factors
inferred← citeshttps://doi.org/10.1007/s10682-021-10104-1openalex-snapshot
Sexual size dimorphism and its allometry in Chinese lizards
inferred← citeshttps://doi.org/10.1007/s10682-024-10295-3openalex-snapshot
Variation in female-biased sexual size dimorphism of northern pike (Esox lucius) associated with environment and life history
inferred← citeshttps://doi.org/10.1007/s10682-025-10347-2openalex-snapshot
Inter-population variation in fin sexual dimorphism in Medaka (Oryzias latipes)
inferred← citeshttps://doi.org/10.1038/s41559-024-02600-8openalex-snapshot
Evolution of sexual size dimorphism in tetrapods is driven by varying patterns of sex-specific selection on size
inferred← citeshttps://doi.org/10.1086/734457openalex-snapshot
Evolutionary Lability of Sexual Selection and Its Implications for Speciation and Macroevolution
inferred← citeshttps://doi.org/10.1086/735583openalex-snapshot
Beyond Size Dimorphism: The Past, Present, and Future of Rensch’s Rule
inferred← citeshttps://doi.org/10.1093/biolinnean/blaa166openalex-snapshot
Latitudinal variation in sexual dimorphism in a freshwater fish group
inferred← citeshttps://doi.org/10.1093/biolinnean/blac136openalex-snapshot
Climate shapes patterns of sexual size and shape dimorphism across the native range of the green anole lizard,Anolis carolinensis(Squamata: Dactyloidae)
inferred← citeshttps://doi.org/10.1093/cz/zoaf033openalex-snapshot
Elevational patterns of sexual size dimorphism in a Mediterranean lizard
inferred← citeshttps://doi.org/10.1101/2022.01.18.476846openalex-snapshot
Bergmann’s rule in Microlophus lizards: testing for latitudinal and climatic gradients of body size
inferred← citeshttps://doi.org/10.1111/1365-2656.14170openalex-snapshot
Viviparity is associated with larger female size and higher sexual size dimorphism in a reproductively bimodal lizard
inferred← citeshttps://doi.org/10.1111/1749-4877.12569openalex-snapshot
Sexual size dimorphism in lizards: Rensch's rule, reproductive mode, clutch size, and line fitting method effects
inferred← citeshttps://doi.org/10.1111/1749-4877.12923openalex-snapshot
Climate and Socio‐Sexual Environment Predict Interpopulation Variation in Chemical Signaling Glands in a Widespread Lizard
inferred← citeshttps://doi.org/10.1111/evo.14049openalex-snapshot
Interspecific allometry for sexual shape dimorphism: Macroevolution of multivariate sexual phenotypes with application to Rensch's rule
inferred← citeshttps://doi.org/10.1111/geb.13230openalex-snapshot
The multiple origins of sexual size dimorphism in global amphibians
inferred← citeshttps://doi.org/10.1111/geb.70076openalex-snapshot
Ecology and Biogeography of Sexual Size Dimorphism in Squamates
inferred← citeshttps://doi.org/10.1111/jbi.13996openalex-snapshot
Latitudinal and environmental patterns of species richness in lizards and snakes across continental North America
inferred← citeshttps://doi.org/10.1111/jbi.70214openalex-snapshot
Geographical Variation in Body Size and Sexual Size Dimorphism ( SSD ) in the Epaulette Shark ( Hemiscyllium ocellatum )
inferred← citeshttps://doi.org/10.1111/jeb.13881openalex-snapshot
Environmental drivers of sexual dimorphism in a lizard with alternative mating strategies
inferred← citeshttps://doi.org/10.1111/mec.17578openalex-snapshot
Evolution of Size‐Fecundity Relationship in Medaka Fish From Different Latitudes
inferred← citeshttps://doi.org/10.2108/zs200114openalex-snapshot
Variation in Mating Behaviors Between a Tropical and a Temperate Species of Medaka Fishes
inferred← citeshttps://doi.org/10.22541/au.166925707.79058806/v1openalex-snapshot
Living in difficult situations: Lizards living in high altitudes have smaller body sizes due to extreme climatic conditions and limited resources
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