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The interplay between natural and sexual selection in the evolution of sexual size dimorphism inSceloporuslizards (Squamata: Phrynosomatidae)
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/ece3.1998openalex-snapshot
Reproductive cycles and reproductive strategies among populations of the Rose‐bellied Lizard Sceloporus variabilis (Squamata: Phrynosomatidae) from central Mexico
inferredcites →https://doi.org/10.1002/ece3.310openalex-snapshot
Atypical reproductive cycles in a population of S celoporus grammicus ( S quamata: P hrynosomatidae) from the M exican P lateau
inferredcites →https://doi.org/10.1006/anbe.1993.1242openalex-snapshot
Contextual signalling and the structure of dyadic encounters in Anolis carolinensis
inferredcites →https://doi.org/10.1006/anbe.1998.1080openalex-snapshot
Female territorial aggression and steroid hormones in mountain spiny lizards
inferredcites →https://doi.org/10.1007/978-3-662-43550-2openalex-snapshot
Modern Phylogenetic Comparative Methods and Their Application in Evolutionary Biology
inferredcites →https://doi.org/10.1007/978-3-662-43550-2_4openalex-snapshot
Graphical Methods for Visualizing Comparative Data on Phylogenies
inferredcites →https://doi.org/10.1007/bf00328427openalex-snapshot
Maternal body-volume as a constraint on reproductive output in lizards: evidence from the evolution of viviparity
inferredcites →https://doi.org/10.1007/s00360-007-0162-7openalex-snapshot
Steroid correlates of multiple color traits in the spiny lizard, Sceloporus pyrocephalus
inferredcites →https://doi.org/10.1007/s10682-008-9242-8openalex-snapshot
A test of Rensch’s rule in dwarf chameleons (Bradypodion spp.), a group with female-biased sexual size dimorphism
inferredcites →https://doi.org/10.1007/s10682-011-9551-1openalex-snapshot
Did sexually dimorphic dorsal coloration evolve by a pre-existing bias in males in the lizard Sceloporus minor?
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/s11692-012-9166-7openalex-snapshot
Is the Evolution of Viviparity Accompanied by a Relative Increase in Maternal Abdomen Size in Lizards?
inferredcites →https://doi.org/10.1016/0003-3472(75)90076-7openalex-snapshot
Comparative aggression in Sceloporus virgatus, S. undulatus consobrinus, and S. u. tristichus (Sauria: Iguanidae)
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.anbehav.2003.02.003openalex-snapshot
Locomotor performance and social dominance in male Anolis cristatellus
inferredcites →https://doi.org/10.1016/j.ympev.2009.09.006openalex-snapshot
Species trees for spiny lizards (Genus Sceloporus): Identifying points of concordance and conflict between nuclear and mitochondrial data
inferredcites →https://doi.org/10.1016/j.ympev.2009.09.008openalex-snapshot
Phylogenetic relationships of phrynosomatid lizards based on nuclear and mitochondrial data, and a revised phylogeny for Sceloporus
inferredcites →https://doi.org/10.1017/cbo9780511608483openalex-snapshot
The Allometry of Growth and Reproduction
inferredcites →https://doi.org/10.1017/s1464793106007007openalex-snapshot
Bivariate line‐fitting methods for allometry
inferredcites →https://doi.org/10.1038/44766openalex-snapshot
Inferring the historical patterns of biological evolution
inferredcites →https://doi.org/10.1046/j.1095-8312.2002.00101.xopenalex-snapshot
Relations between microhabitat use and limb shape in phrynosomatid lizards
inferredcites →https://doi.org/10.1086/284325openalex-snapshot
Phylogenies and the Comparative Method
inferredcites →https://doi.org/10.1086/286013openalex-snapshot
Phylogenies and the Comparative Method: A General Approach to Incorporating Phylogenetic Information into the Analysis of Interspecific Data
inferredcites →https://doi.org/10.1086/393620openalex-snapshot
The Evolution of Body Size: What Keeps Organisms Small?
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/10.1093/acprof:oso/9780199208784.001.0001openalex-snapshot
Sex, Size and Gender Roles
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/acprof:oso/9780199208784.003.0008openalex-snapshot
Sexual size dimorphism in spiders: patterns and processes
inferredcites →https://doi.org/10.1093/beheco/arl001openalex-snapshot
Female-specific color is a signal of quality in the striped plateau lizard (Sceloporus virgatus)
inferredcites →https://doi.org/10.1093/beheco/arm041openalex-snapshot
Sex and social costs of escaping in the striped plateau lizard Sceloporus virgatus
inferredcites →https://doi.org/10.1093/bioinformatics/btg412openalex-snapshot
APE: Analyses of Phylogenetics and Evolution in R language
inferredcites →https://doi.org/10.1093/molbev/msw054openalex-snapshot
MEGA7: Molecular Evolutionary Genetics Analysis Version 7.0 for Bigger Datasets
inferredcites →https://doi.org/10.1093/nar/gkh340openalex-snapshot
MUSCLE: multiple sequence alignment with high accuracy and high throughput
inferredcites →https://doi.org/10.1093/oso/9780198546412.001.0001openalex-snapshot
The Comparative Method in Evolutionary Biology
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a003974openalex-snapshot
Estimating Absolute Rates of Molecular Evolution and Divergence Times: A Penalized Likelihood Approach
inferredcites →https://doi.org/10.1093/sysbio/sys029openalex-snapshot
MrBayes 3.2: Efficient Bayesian Phylogenetic Inference and Model Choice Across a Large Model Space
inferredcites →https://doi.org/10.1111/2041-210x.12066openalex-snapshot
Two new graphical methods for mapping trait evolution on phylogenies
inferredcites →https://doi.org/10.1111/azo.12037openalex-snapshot
Reproduction and sexual dimorphism in two populations of the polymorphic spiny lizard S celoporus minor from H idalgo, M éxico
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/evo.12053openalex-snapshot
DIVERSITY AND NICHE EVOLUTION ALONG ARIDITY GRADIENTS IN NORTH AMERICAN LIZARDS (PHRYNOSOMATIDAE)
inferredcites →https://doi.org/10.1111/j.0014-3820.2002.tb01464.xopenalex-snapshot
SEXUAL DIMORPHISM IN LIZARD BODY SHAPE: THE ROLES OF SEXUAL SELECTION AND FECUNDITY SELECTION
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.0014-3820.2004.tb01684.xopenalex-snapshot
PHYLOGENETIC COMPARATIVE ANALYSIS OF LIFE-HISTORY VARIATION AMONG POPULATIONS OF THE LIZARD SCELOPORUS UNDULATUS: AN EXAMPLE AND PROGNOSIS
inferredcites →https://doi.org/10.1111/j.1439-0310.1998.tb00071.xopenalex-snapshot
Morphological and Behavioural Traits Affecting the Intensity and Outcome of Male Contests inGallotia galloti galloti(Family Lacertidae)
inferredcites →https://doi.org/10.1111/j.1439-0310.2005.01147.xopenalex-snapshot
Behavioral Causes and Consequences of Sexual Size Dimorphism
inferredcites →https://doi.org/10.1111/j.1558-5646.1990.tb05225.xopenalex-snapshot
THE EVOLUTION OF FORM AND FUNCTION: MORPHOLOGY AND LOCOMOTOR PERFORMANCE IN WEST INDIAN ANOLIS LIZARDS
inferredcites →https://doi.org/10.1111/j.1558-5646.1998.tb02259.xopenalex-snapshot
THE EVOLUTION OF FEMALE-BIASED SEXUAL SIZE DIMORPHISM: A POPULATION-LEVEL COMPARATIVE STUDY IN HORNED LIZARDS (PHRYNOSOMA)
inferredcites →https://doi.org/10.1111/j.1558-5646.1999.tb04570.xopenalex-snapshot
MOLECULAR PHYLOGENETICS AND EVOLUTION OF SEXUAL DICHROMATISM AMONG POPULATIONS OF THE YARROW'S SPINY LIZARD (SCELOPORUS JARROVII)
inferredcites →https://doi.org/10.1111/j.2041-210x.2010.00044.xopenalex-snapshot
Phylogenetic signal and linear regression on species data
inferredcites →https://doi.org/10.1111/j.2041-210x.2011.00153.xopenalex-snapshot
smatr 3– an R package for estimation and inference about allometric lines
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/mec.13122openalex-snapshot
Estimating the temporal and spatial extent of gene flow among sympatric lizard populations (genus Sceloporus ) in the southern Mexican highlands
inferredcites →https://doi.org/10.1139/z84-260openalex-snapshot
Desert lizard reproduction: seasonal and annual variation in Urosaurus ornatus (Iguanidae)
inferredcites →https://doi.org/10.1146/annurev-ento-112408-085500openalex-snapshot
Sex Differences in Phenotypic Plasticity Affect Variation in Sexual Size Dimorphism in Insects: From Physiology to Evolution
inferredcites →https://doi.org/10.1146/annurev-ento-120710-100604openalex-snapshot
Group Size and Its Effects on Collective Organization
inferredcites →https://doi.org/10.1146/annurev.ecolsys.28.1.659openalex-snapshot
Allometry for Sexual Size Dimorphism: Pattern and Process in the Coevolution of Body Size in Males and Females
inferredcites →https://doi.org/10.1146/annurev.ecolsys.36.102003.152631openalex-snapshot
Life-History Evolution in Reptiles
inferredcites →https://doi.org/10.11646/zootaxa.1800.1.1openalex-snapshot
A monographic catalogue on the systematics and phylogeny of the South American iguanian lizard family Liolaemidae (Squamata, Iguania)
inferredcites →https://doi.org/10.1186/1471-2148-14-82openalex-snapshot
Selecting optimal partitioning schemes for phylogenomic datasets
inferredcites →https://doi.org/10.1186/s12862-014-0204-1openalex-snapshot
Strong genetic structure corresponds to small-scale geographic breaks in the Australian alpine grasshopper Kosciuscola tristis
inferredcites →https://doi.org/10.1186/s12862-016-0628-xopenalex-snapshot
Phylogenomics of a rapid radiation: is chromosomal evolution linked to increased diversification in north american spiny lizards (Genus Sceloporus)?
inferredcites →https://doi.org/10.13128/acta_herpetol-10472openalex-snapshot
Reproductive strategy of male and female eastern spiny lizards Sceloporus spinosus (Squamata: Phrynosomatidae) from a region of the Chihuahuan Desert, México
inferredcites →https://doi.org/10.1371/journal.pone.0000897openalex-snapshot
Only Half Right: Species with Female-Biased Sexual Size Dimorphism Consistently Break Rensch's Rule
inferredcites →https://doi.org/10.1371/journal.pone.0011495openalex-snapshot
Identification of Pathway-Biased and Deleterious Melatonin Receptor Mutants in Autism Spectrum Disorders and in the General Population
inferredcites →https://doi.org/10.1371/journal.pone.0014355openalex-snapshot
Sex, Ecology and the Brain: Evolutionary Correlates of Brain Structure Volumes in Tanganyikan Cichlids
inferredcites →https://doi.org/10.1371/journal.pone.0093197openalex-snapshot
Female Preference for Sympatric vs. Allopatric Male Throat Color Morphs in the Mesquite Lizard (Sceloporus grammicus) Species Complex
inferredcites →https://doi.org/10.1371/journal.pone.0145248openalex-snapshot
Body Size Adaptations to Altitudinal Climatic Variation in Neotropical Grasshoppers of the Genus Sphenarium (Orthoptera: Pyrgomorphidae)
inferredcites →https://doi.org/10.1515/9781400863945.117openalex-snapshot
Chapter 6. Phylogenetic Perspectives on the Evolution of Lizard Territoriality
inferredcites →https://doi.org/10.15517/rbt.v47i4.19317openalex-snapshot
Reproductive characteristics of the black-tailed brush lizard, Urosaurus nigricaudus (Phrynosomatidae)
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/10.1655/0733-1347(2007)20[147:eoerit]2.0.co;2openalex-snapshot
EVOLUTION OF EGG RETENTION IN THE SCELOPORUS SPINOSUS GROUP: EXPLORING THE ROLE OF PHYSIOLOGICAL, ENVIRONMENTAL, AND PHYLOGENETIC FACTORS
inferredcites →https://doi.org/10.1670/0022-1511(2002)036[0036:rcotsl]2.0.co;2openalex-snapshot
Reproductive Characteristics of the Spiny Lizards, Sceloporus horridus and Sceloporus spinosus (Squamata: Phrynosomatidae) from México
inferredcites →https://doi.org/10.1670/0022-1511(2003)037[0001:reosus]2.0.co;2openalex-snapshot
Reproductive Ecology of Sceloporus utiformis (Sauria: Phrynosomatidae) from a Tropical Dry Forest of México
inferredcites →https://doi.org/10.1670/08-140r1.1openalex-snapshot
Reproductive Activity of Three Sympatric Viviparous Lizards at Omiltemi, Guerrero, Sierra Madre del Sur, Mexico
inferredcites →https://doi.org/10.1670/200-01aopenalex-snapshot
Reproduction in the Boulder Spiny Lizard, Sceloporus pyrocephalus (Sauria: Phrynosomatidae), from a Tropical Dry Forest of México
inferredcites →https://doi.org/10.1890/0012-9615(2002)072[0541:msdssa]2.0.co;2openalex-snapshot
MULTIVARIATE SEXUAL DIMORPHISM, SEXUAL SELECTION, AND ADAPTATION IN GREATER ANTILLEAN ANOLIS LIZARDS
inferredcites →https://doi.org/10.1894/0038-4909(2003)048<0123:bssdac>2.0.co;2openalex-snapshot
BODY SIZE, SEXUAL DIMORPHISM, AND CLUTCH SIZE IN TWO POPULATIONS OF THE LIZARD SCELOPORUS OCHOTERANAE
inferredcites →https://doi.org/10.1894/0038-4909(2005)050[0178:rcosgs]2.0.co;2openalex-snapshot
REPRODUCTIVE CYCLE OF SCELOPORUS GRAMMICUS (SQUAMATA: PHRYNOSOMATIDAE) FROM TEOTIHUACÁN, MÉXICO
inferredcites →https://doi.org/10.1894/0038-4909(2006)51[157:rcomaf]2.0.co;2openalex-snapshot
REPRODUCTIVE CYCLE OF MALE AND FEMALE SPINY LIZARDS, SCELOPORUS MELANORHINUS, IN A TROPICAL DRY FOREST
inferredcites →https://doi.org/10.1894/0038-4909(2007)52[600:eotsls]2.0.co;2openalex-snapshot
ECOLOGY OF THE SPINY LIZARD SCELOPORUS JARROVII IN THE CENTRAL CHIHUAHUAN DESERT
inferredcites →https://doi.org/10.1894/0038-4909-58.1.54openalex-snapshot
Reproductive Cycle of a High-Elevation, Oviparous Lizard (Sceloporus spinosus: Reptilia: Phrynosomatidae)
inferredcites →https://doi.org/10.1894/gc-164.1openalex-snapshot
Reproductive Characteristics of a Population of Sceloporus dugesii (Squamata: Phrynosomatidae) from Michoacán, Mexico
inferredcites →https://doi.org/10.21829/azm.2003.902553openalex-snapshot
An annotated list of the species-group names applied to the lizard genus Sceloporus
inferredcites →https://doi.org/10.21829/azm.2004.2022335openalex-snapshot
Infestación y distribución corporal de la nigua Eutrombicula alfreddugesi (Acari: Trombiculidae) en el lacertilio de las rocas Sceloporus couchii (Sauria: Phrynosomatidae)
inferredcites →https://doi.org/10.21829/azm.2005.2131974openalex-snapshot
CICLO REPRODUCTOR DE SCELOPORUS POINSETTII BAIRD Y GIRARD 1852 (SQUAMATA: PHRYNOSOMATIDAE) EN EL CENTRO DEL DESIERTO CHIHUAHUENSE, MÉXICO
inferredcites →https://doi.org/10.22201/ib.20078706e.2011.2.471openalex-snapshot
Ciclo reproductor de Sceloporus ochoterenae en el estado de Morelos, México
inferredcites →https://doi.org/10.2307/1439090openalex-snapshot
The Mexican and Central American Lizards of the Genus Sceloporus
inferredcites →https://doi.org/10.2307/1441282openalex-snapshot
Reproduction in the Granite Spiny Lizard, Sceloporus orcutti
inferredcites →https://doi.org/10.2307/1442682openalex-snapshot
Reproductive Ecology of the Florida Scrub Lizard, Sceloporus woodi
inferredcites →https://doi.org/10.2307/1442967openalex-snapshot
A Population Analysis of the Sagebrush Lizard, Sceloporus graciosus in Southern Utah
inferredcites →https://doi.org/10.2307/1466998openalex-snapshot
Modeling Dominance: The Influence of Size, Coloration, and Experience on Dominance Relations in Tree Lizards (Urosaurus ornatus)
inferredcites →https://doi.org/10.2307/1467007openalex-snapshot
Phylogeny of the Spiny Lizards (Sceloporus) Based on Molecular and Morphological Evidence
inferredcites →https://doi.org/10.2307/1467079openalex-snapshot
Reproduction and Lipid Utilization of Tropical Populations of Sceloporus variabilis
inferredcites →https://doi.org/10.2307/1564933openalex-snapshot
The Reproductive Cycle of the Viviparous Mexican Lizard Sceloporus torquatus
inferredcites →https://doi.org/10.2307/1565712openalex-snapshot
Variation in Clutch Size and Offspring Size Relative to Environmental Conditions in the Lizard Sceloporus virgatus
inferredcites →https://doi.org/10.2307/1566029openalex-snapshot
Diet and Reproductive Biology of the Viviparous Lizard Sceloporus torquatus torquatus (Squamata: Phrynosomatidae)
inferredcites →https://doi.org/10.2307/1934336openalex-snapshot
Comparative Demography of Two Viviparous Iguanid Lizards (Sceloporus Jarrovi and Sceloporus Poinsetti)
inferredcites →https://doi.org/10.2307/1935309openalex-snapshot
Demography of the Striped Plateau Lizard, Sceloporus Virgatus
inferredcites →https://doi.org/10.2307/1937584openalex-snapshot
Elevational Covariation in Environmental Constraints and Life Histories of the Desert Lizard Sceloporus Merriami
inferredcites →https://doi.org/10.2307/2424171openalex-snapshot
Life History Phenomena in Two Populations of the Lizard Sceloporus undulatus in Southwestern New Mexico
inferredcites →https://doi.org/10.2307/3545893openalex-snapshot
Sexual Dimorphism in Lacertid Lizards: Male Head Increase vs Female Abdomen Increase?
inferredcites →https://doi.org/10.32614/cran.package.caperopenalex-snapshot
caper: Comparative Analyses of Phylogenetics and Evolution in R
inferredcites →https://doi.org/10.3398/064.069.0403openalex-snapshot
Reproductive Cycle of the LizardSceloporus mucronatuswith Comments on Intraspecific Geographic Variation
inferredcites →https://doi.org/10.3398/1527-0904(2007)67[492:gadoop]2.0.co;2openalex-snapshot
GROWTH AND DEMOGRAPHY OF ONE POPULATION OF THE LIZARD SCELOPORUS MUCRONATUS MUCRONATUS
inferredcites →https://doi.org/10.4067/s0716-078x2009000400009openalex-snapshot
Sexual dimorphism and reproductive cycle in the arboreal spiny lizard Sceloporus formosus Wiegmann (Squamata: Phrynosomatidae) from central Oaxaca, México
inferredcites →https://doi.org/10.5281/zenodo.13464657openalex-snapshot
Die Abhängigkeit der relativen Sexualdifferenz von der Körpergröße
inferredcites →https://doi.org/10.5860/choice.29-5104openalex-snapshot
The comparative method in evolutionary biology
inferredcites →https://doi.org/10.5860/choice.44-0314openalex-snapshot
Sexual segregation in vertebrates: ecology of the two sexes
inferredcites →https://doi.org/10.5860/choice.45-3188openalex-snapshot
Sex, size, and gender roles: evolutionary studies of sexual size dimorphism
inferredcites →https://doi.org/10.5962/bhl.part.17244openalex-snapshot
Sexual size differences in the genus Sceloporus
inferredcites →https://doi.org/10.5962/bhl.title.16254openalex-snapshot
Variation in clutch and litter size in New World reptiles
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.39.e178597zenodo-depositor-declared
It's not all about size: sexual size dimorphism and caudal autotomy of Campbell's Alligator Lizard, Abronia campbelli Brodie & Savage, 1993
inferred← citeshttps://doi.org/10.1002/ece3.10590openalex-snapshot
Chigger mite (Eutrombicula alfreddugesi) ectoparasitism does not contribute to sex differences in growth rate in eastern fence lizards (Sceloporus undulatus)
inferred← citeshttps://doi.org/10.1002/ece3.3986openalex-snapshot
Function‐related Drivers of Skull Morphometric Variation and Sexual Size Dimorphism in a Subterranean Rodent, Plateau Zokor (Eospalax baileyi)
inferred← citeshttps://doi.org/10.1002/ece3.6897openalex-snapshot
Influence of size, sex, and reproductive status on the thermal biology of endemic Florida scrub lizards
inferred← citeshttps://doi.org/10.1002/ece3.70594openalex-snapshot
Evolutionary Links Between Skull Shape and Body Size Suggest Allometric Forces and Selection at Work in a Generalist Group of Lizards
inferred← citeshttps://doi.org/10.1002/ece3.71709openalex-snapshot
Rethinking Phenotypic Categorization: Evidence From Morphological and Life‐History Traits in Spiny Lizards ( Sceloporus )
inferred← citeshttps://doi.org/10.1002/ece3.71858openalex-snapshot
Sexual Size Dimorphism in Rays and Skates (Elasmobranchii: Batoidea)
inferred← citeshttps://doi.org/10.1002/ece3.7237openalex-snapshot
Occurrence data uncover patterns of allopatric divergence and interspecies interactions in the evolutionary history of Sceloporus lizards
inferred← citeshttps://doi.org/10.1002/ece3.9066openalex-snapshot
Exploring the interplay between natural and intersexual selection on the evolution of a cognitive trait
inferred← citeshttps://doi.org/10.1002/gcb4.70055openalex-snapshot
Contrasting Climate‐Associated Shifts in Male and Female Body Size Reduce Sexual Size Dimorphism in the Sagebrush Lizard ( Sceloporus graciosus )
inferred← citeshttps://doi.org/10.1007/s00435-025-00731-5openalex-snapshot
Insights into Secondary Sexual Dimorphism in a Northeastern Brazilian population of Bogert’s gecko, Phyllopezus lutzae
inferred← citeshttps://doi.org/10.1007/s10682-021-10104-1openalex-snapshot
Sexual size dimorphism and its allometry in Chinese lizards
inferred← citeshttps://doi.org/10.1016/j.jaridenv.2023.104985openalex-snapshot
The lizard with kaleidoscope eyes: Population characteristics of the Namib web-footed gecko, Pachydactylus rangei
inferred← citeshttps://doi.org/10.1016/j.zool.2020.125781openalex-snapshot
Sexual dimorphism in size and shape among populations of the lizard Sceloporus variabilis (Squamata: Phrynosomatidae)
inferred← citeshttps://doi.org/10.1016/j.zool.2026.126337openalex-snapshot
Is developmental instability sex-specific? Case study in two spiny lizards with different reproductive modes
inferred← citeshttps://doi.org/10.1016/j.zool.2026.126350openalex-snapshot
Influence of population density and vegetation on the expression of ventral ornaments in male Sceloporus lizards
inferred← citeshttps://doi.org/10.1038/s41467-022-30535-wopenalex-snapshot
Exceptional parallelisms characterize the evolutionary transition to live birth in phrynosomatid lizards
inferred← citeshttps://doi.org/10.1038/s41467-024-50386-xopenalex-snapshot
Sexual size dimorphism in mammals is associated with changes in the size of gene families related to brain development
inferred← citeshttps://doi.org/10.1073/pnas.2309825120openalex-snapshot
Fossil evidence sheds light on sexual selection during the early evolution of birds
inferred← citeshttps://doi.org/10.1093/biolinnean/blab169openalex-snapshot
Variation in size and shape sexual dimorphism in the Sceloporus scalaris species group (Squamata: Phrynosomatidae) from the Transvolcanic Belt of Mexico
inferred← citeshttps://doi.org/10.1093/biolinnean/blad051openalex-snapshot
Fashion or function? Relaxed selection and stasis are key features of the evolution of stripes, bands and collars in Sceloporus lizards (Squamata: Phrynosomatidae)
inferred← citeshttps://doi.org/10.1093/biolinnean/blaf109openalex-snapshot
Habitat use and morphological evolution in Sceloporus : a single- and multi-trait comparative analysis
inferred← citeshttps://doi.org/10.1093/cz/zoac033openalex-snapshot
Sexual size monomorphism may evolve in lizards with a body size maximizing reproductive performance for both sexes
inferred← citeshttps://doi.org/10.1093/cz/zoaf033openalex-snapshot
Elevational patterns of sexual size dimorphism in a Mediterranean lizard
inferred← citeshttps://doi.org/10.1093/cz/zoy007openalex-snapshot
Multiple color patches and parasites in Sceloporus occidentalis: differential relationships by sex and infection
inferred← citeshttps://doi.org/10.1093/iob/obac025openalex-snapshot
Species-Specific Expression of Growth-Regulatory Genes in 2 Anoles with Divergent Patterns of Sexual Size Dimorphism
inferred← citeshttps://doi.org/10.1093/jhered/esad046openalex-snapshot
Species differences in hormonally mediated gene expression underlie the evolutionary loss of sexually dimorphic coloration inSceloporuslizards
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/10.1111/1749-4877.12779openalex-snapshot
Trophic niche and adaptation in highland lizards: sex has greater influences than species matching
inferred← citeshttps://doi.org/10.1111/azo.12258openalex-snapshot
Lack of spermatogenic variation in a polymorphic lizard, Sceloporus aeneus (Squamata: Phrynosomatidae)
inferred← citeshttps://doi.org/10.1111/azo.12315openalex-snapshot
Reproduction and sexual dimorphism in the viviparous lizard Sceloporus palaciosi (Squamata: Phrynosomatidae) from the Trans‐Mexican Volcanic Belt, Mexico
inferred← citeshttps://doi.org/10.1111/azo.12329openalex-snapshot
Sexual dimorphism in size and shape in the viviparous lizard Abronia taeniata (Squamata: Anguidae) in central Mexico
inferred← citeshttps://doi.org/10.1111/azo.12342openalex-snapshot
Reproduction in Sceloporus licki (Reptilia: Phrynosomatidae) in the Cape Region, Baja California Sur
inferred← citeshttps://doi.org/10.1111/ele.14515openalex-snapshot
Pre‐Copulatory Sexual Selection Predicts Sexual Size Dimorphism: A Meta‐Analysis of Comparative Studies
inferred← citeshttps://doi.org/10.1111/geb.13255openalex-snapshot
Rensch’s rule—Definitions and statistics
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.13067openalex-snapshot
The fast‐slow life‐history continuum in insular lizards: a comparison between species with invariant and variable clutch sizes
inferred← citeshttps://doi.org/10.1139/cjz-2018-0263openalex-snapshot
High-mountain altitudinal gradient influences thermal ecology of the Mesquite Lizard ( Sceloporus grammicus )
inferred← citeshttps://doi.org/10.1163/1568539x-00003469openalex-snapshot
Mating system, male territoriality and agility as predictors of the evolution of sexual size dimorphism in hummingbirds (Aves: Trochilidae)
inferred← citeshttps://doi.org/10.1186/s12862-018-1299-6openalex-snapshot
Macroevolution of sexual size dimorphism and reproduction-related phenotypic traits in lizards of the Chaco Domain
inferred← citeshttps://doi.org/10.15414/afz.2023.26.03.263-272openalex-snapshot
Sexual dimorphism and dietary composition of the sandfish lizard Scincus scincus (Linnaeus, 1758) of southeastern Algeria
inferred← citeshttps://doi.org/10.15446/abc.v26n3.88388openalex-snapshot
DIMORFISMO SEXUAL EN TAMAÑO Y FORMA EN UNA POBLACIÓN DE ESCÍNCIDOS DE COLA AZUL DEL GÉNERO Plestiodon (SCINCIDAE)
inferred← citeshttps://doi.org/10.1643/ce-18-135openalex-snapshot
The Allometry of Sexual Dimorphism in Sceloporus formosus (Squamata: Phrynosomatidae)
inferred← citeshttps://doi.org/10.1655/herpetologica-d-22-00008openalex-snapshot
Sexual Dimorphism in Namibian Endemic Herero Nama Lizards ( Namazonurus pustulatus)
inferred← citeshttps://doi.org/10.22201/fc.25942158e.2026.2.1670openalex-snapshot
TAMAÑO MÁXIMO DE LA LAGARTIJA ESPINOSA DE HUNSAKER, Sceloporus hunsakeri (SQUAMATA: PHRYNOSOMATIDAE), UNA ESPECIE ENDÉMICA DE MÉXICO
inferred← citeshttps://doi.org/10.22541/au.167342626.60283320/v1openalex-snapshot
Sexual dimorphism in morphology and bite force in the mountain dragon, Diploderma batangense (Squamata: Anguidae), from the Hengduan Mountains in western China
inferred← citeshttps://doi.org/10.2994/sajh-d-18-00056.1openalex-snapshot
Sexual Dimorphism and Feeding Ecology of the Black-bellied Bunchgrass Lizard Sceloporus aeneus (Squamata: Phrynosomatidae) in Central Mexico
inferred← citeshttps://doi.org/10.2994/sajh-d-20-00010.1openalex-snapshot
Reproductive Strategies in Relation to Maternal Phenotype in a Model Lizard (Salvator merianae)
inferred← citeshttps://doi.org/10.2994/sajh-d-20-00025.1openalex-snapshot
Season, Body Condition, and Sex Variation of Ectoparasite Abundance in Tarentola delalandii (Squamata: Phyllodactylidae) from Two Ecologically Contrasting Populations of Tenerife (Canary Islands)
inferred← citeshttps://doi.org/10.3389/fevo.2022.1016885openalex-snapshot
Sexual and natural selection interplay in sexual head shape dimorphism of two sympatric racerunners (Squamata: Lacertidae)
inferred← citeshttps://doi.org/10.3390/ani14233373openalex-snapshot
Life–History Traits of Eremias pleskei Nikolsky, 1905 from Northeastern Anatolia
inferred← citeshttps://doi.org/10.3897/vz.71.e71995openalex-snapshot
Hidden diversity within a polytypic species: The enigmatic Sceloporus torquatus Wiegmann, 1828 (Reptilia, Squamata, Phrynosomatidae)
inferred← citeshttps://doi.org/10.3897/vz.73.e94004openalex-snapshot
Allometric analysis of sexual dimorphism and morphological variation in two chromosome races of the Sceloporus grammicus complex (Squamata: Phrynosomatidae) from Mexico
inferred← citeshttps://doi.org/10.46309/biodicon.2021.991685openalex-snapshot
Body size and age structure of Lacerta agilis LINNAEUS, 1758 (Reptilia: Lacertidae) from two different populations in Turkey
inferred← citeshttps://doi.org/10.5358/hsj.39.19openalex-snapshot
Sexual Dimorphism and Reproductive Characteristics of the Cozumel Spiny Lizard, Sceloporus cozumelae (Squamata: Phrynosomatidae) from Mexico
inferred← citeshttps://doi.org/10.5358/hsj.44.210openalex-snapshot
Sexual Size Dimorphism of Two Species of the Sceloporus Pyrocephalus Species Group from Mexico
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