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Size-Dependent Selective Mechanisms on Males and Females and the Evolution of Sexual Size Dimorphism in Frogs

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What this work says

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

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Defining sexual selection as sex-dependent selection

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inferredcites →https://doi.org/10.1073/pnas.0404503101openalex-snapshot

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inferredcites →https://doi.org/10.1086/284325openalex-snapshot

Phylogenies and the Comparative Method

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/10.1086/673282openalex-snapshot

Correlated Evolution of Allometry and Sexual Dimorphism across Higher Taxa

inferredcites →https://doi.org/10.1093/icb/24.2.397openalex-snapshot

Alternative Mating Behaviors of Young Male Bullfrogs

inferredcites →https://doi.org/10.1093/sysbio/41.1.18openalex-snapshot

Procedures for the Analysis of Comparative Data Using Phylogenetically Independent Contrasts

inferredcites →https://doi.org/10.1093/sysbio/42.4.569openalex-snapshot

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Extreme lifespan of the human fish ( Proteus anguinus ): a challenge for ageing mechanisms

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Detecting correlated evolution on phylogenies: a general method for the comparative analysis of discrete characters

inferredcites →https://doi.org/10.1098/rspb.2002.2170openalex-snapshot

Sexual size dimorphism in anurans

inferredcites →https://doi.org/10.1098/rspb.2007.1043openalex-snapshot

Sexual selection explains Rensch's rule of allometry for sexual size dimorphism

inferredcites →https://doi.org/10.1098/rstb.1995.0078openalex-snapshot

A composite estimate of primate phylogeny

inferredcites →https://doi.org/10.1111/(issn)1095-8312openalex-snapshot

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A COMPARATIVE TEST OF ADAPTIVE HYPOTHESES FOR SEXUAL SIZE DIMORPHISM IN LIZARDS

inferredcites →https://doi.org/10.1111/j.1095-8312.2008.01035.xopenalex-snapshot

The evolution of sexual size dimorphism in cottontail rabbits (Sylvilagus, Leporidae)

inferredcites →https://doi.org/10.1111/j.1095-8312.2010.01430.xopenalex-snapshot

A test of Rensch's rule in varanid lizards

inferredcites →https://doi.org/10.1111/j.1365-2907.2005.00045.xopenalex-snapshot

Potential causes and life‐history consequences of sexual size dimorphism in mammals

inferredcites →https://doi.org/10.1111/j.1420-9101.2008.01567.xopenalex-snapshot

Sexual selection, sexual size dimorphism and Rensch’s rule in Odonata

inferredcites →https://doi.org/10.1111/j.1420-9101.2009.01768.xopenalex-snapshot

Evolution of sexual size monomorphism: the influence of passive mate guarding

inferredcites →https://doi.org/10.1111/j.1558-5646.1994.tb05313.xopenalex-snapshot

SEXUAL SELECTION IN AMERICAN TOADS: A TEST OF A GOOD‐GENES HYPOTHESIS

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/jeb.12349openalex-snapshot

Ecological divergence and sexual selection drive sexual size dimorphism in new world pitvipers (Serpentes: Viperidae)

inferredcites →https://doi.org/10.1111/jzo.12137openalex-snapshot

R ensch's rule and sexual dimorphism in salamanders: patterns and potential processes

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

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Comportamento territorial e de acasalamento de Phyllomedusa azurea (Anura, Hylidae) em uma lagoa temporária do centro-oeste do Brasil

inferredcites →https://doi.org/10.1163/1568538054253375openalex-snapshot

Breeding activity patterns, reproductive modes, and habitat use by anurans (Amphibia) in a seasonal environment in the Pantanal, Brazil

inferredcites →https://doi.org/10.1163/15685381-00002836openalex-snapshot

Habitat use, reproductive traits and social interactions in a stream-dweller treefrog endemic to the Brazilian Cerrado

inferredcites →https://doi.org/10.1163/156853888x00035openalex-snapshot

Multiple clutches, egg mortality and mate choice in the mid-wife toad, Alytes obstetricans

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/10.1186/1471-2148-13-27openalex-snapshot

Does life history shape sexual size dimorphism in anurans? A comparative analysis

inferredcites →https://doi.org/10.1186/1742-9994-10-10openalex-snapshot

Sexual size dimorphism in anurans fails to obey Rensch’s rule

inferredcites →https://doi.org/10.1206/0003-0090(2005)294[0001:srotff]2.0.co;2openalex-snapshot

SYSTEMATIC REVIEW OF THE FROG FAMILY HYLIDAE, WITH SPECIAL REFERENCE TO HYLINAE: PHYLOGENETIC ANALYSIS AND TAXONOMIC REVISION

inferredcites →https://doi.org/10.1206/0003-0090(2006)297[0001:tatol]2.0.co;2openalex-snapshot

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inferredcites →https://doi.org/10.1206/834.1openalex-snapshot

Phylogeny, Taxonomic Revision, and Character Evolution of the Genera Chiasmocleis and Syncope (Anura, Microhylidae) in Amazonia, with Descriptions of Three New Species

inferredcites →https://doi.org/10.1590/s0031-10492007001300001openalex-snapshot

Comportamento reprodutivo e seleção sexual em Dendropsophus bipunctatus (Spix, 1824) (Anura, 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/10.1643/ce-05-294openalex-snapshot

Strategic Male Calling Behavior in an Australian Terrestrial Toadlet (Pseudophryne Bibronii)

inferredcites →https://doi.org/10.1644/09-mamm-a-018.1openalex-snapshot

Cranial sexual dimorphism in New World marsupials and a test of Rensch's rule in Didelphidae

inferredcites →https://doi.org/10.1670/0022-1511(2003)037[0354:tsilfa]2.0.co;2openalex-snapshot

Testes Size in Leptodactylid Frogs and Occurrence of Multimale Spawning in the Genus Leptodactylus in Brazil

inferredcites →https://doi.org/10.1890/0012-9658(1999)080[2555:idlars]2.0.co;2openalex-snapshot

INDIVIDUAL DIFFERENCES, LONGEVITY, AND REPRODUCTIVE SENESCENCE IN BIGHORN EWES

inferredcites →https://doi.org/10.2307/1443418openalex-snapshot

Sexual Selection and Sexual Dimorphism in the Amphibia

inferredcites →https://doi.org/10.2307/1446982openalex-snapshot

Sexual Size Dimorphism in Snakes Revisited

inferredcites →https://doi.org/10.2307/1564657openalex-snapshot

Satellite Behavior in the Neotropical Treefrog Hyla minuta

inferredcites →https://doi.org/10.2307/1565172openalex-snapshot

Breeding Activity of the Neotropical Treefrog Hyla elegans (Anura, Hylidae)

inferredcites →https://doi.org/10.2307/2387922openalex-snapshot

Reproductive Behavior and Male Mating Success in a Neotropical Toad, Bufo typhonius

inferredcites →https://doi.org/10.2307/2408361openalex-snapshot

Proximate Mechanisms of Sexual Selection in Wood Frogs

inferredcites →https://doi.org/10.2307/4080883openalex-snapshot

Bonner Zoologische Beiträge

inferredcites →https://doi.org/10.2307/j.ctvh1djdq.10openalex-snapshot

Growth, development and aging

inferredcites →https://doi.org/10.33256/hjopenalex-snapshot

The Herpetological Journal

inferredcites →https://doi.org/10.7208/chicago/9780226893334.001.0001openalex-snapshot

The Ecology and Behavior of Amphibians

What points at this work

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

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inferred← citeshttps://doi.org/10.1002/ece3.3450openalex-snapshot

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inferred← citeshttps://doi.org/10.1002/ece3.9953openalex-snapshot

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inferred← citeshttps://doi.org/10.1007/s00265-023-03418-3openalex-snapshot

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inferred← citeshttps://doi.org/10.1007/s10682-023-10280-2openalex-snapshot

Intraspecific divergence of sexual size dimorphism and reproductive strategies in a polytypic poison frog

inferred← citeshttps://doi.org/10.1007/s10682-024-10306-3openalex-snapshot

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inferred← citeshttps://doi.org/10.1007/s11692-020-09509-7openalex-snapshot

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Egg-laying site, fecundity and degree of sexual size dimorphism in frogs

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inferred← citeshttps://doi.org/10.1093/jhered/esaa019openalex-snapshot

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Sexual dimorphism in Scutiger boulengeri, an endemic toad from the Tibetan Plateau

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Phenotypic integration mediated by hormones: associations among digit ratios, body size and testosterone during tadpole development

inferred← citeshttps://doi.org/10.1186/s12983-021-00425-wopenalex-snapshot

Life history traits and reproductive ecology of North American chorus frogs of the genus Pseudacris (Hylidae)

inferred← citeshttps://doi.org/10.1371/journal.pone.0149879openalex-snapshot

Bigger Is Not Always Better: Females Prefer Males of Mean Body Size in Philautus odontotarsus

inferred← citeshttps://doi.org/10.1371/journal.pone.0246401openalex-snapshot

A new reproductive mode in anurans: Natural history of Bokermannohyla astartea (Anura: Hylidae) with the description of its tadpole and vocal repertoire

inferred← citeshttps://doi.org/10.1655/herpetologica-d-19-00070openalex-snapshot

Reproductive Biology and Sexual Dimorphism in Bokermannohyla alvarengai (Anura: Hylidae)

inferred← citeshttps://doi.org/10.1670/20-027openalex-snapshot

Reproductive Phenology of Five Species of Terrestrial Frogs (Genus Eleutherodactylus) from Cuba

inferred← citeshttps://doi.org/10.25225/fozo.v66.i1.a4.2017openalex-snapshot

Sexual dimorphism in size and shape of traits related to locomotion in nine anuran species from Serbia and Montenegro

inferred← citeshttps://doi.org/10.2984/74.1.4openalex-snapshot

Vocal Repertoire and Extreme Sexual Size Dimorphism in the Fijian Ground Frog Cornufer vitianus (Anura, Ceratobatrachidae)1

inferred← citeshttps://doi.org/10.2994/sajh-d-17-00039.1openalex-snapshot

Sexual Dimorphism in Bokermannohyla martinsi (Bokermann, 1964) (Anura, Hylidae) with a Report of Male–Male Combat

inferred← citeshttps://doi.org/10.2994/sajh-d-17-00060.1openalex-snapshot

Reproductive Cycle, Size and Age at Sexual Maturity, and Sexual Dimorphism in the Stream-Breeding Frog Crossodactylus schmidti (Hylodidae)

inferred← citeshttps://doi.org/10.31274/etd-20210609-82openalex-snapshot

Macroevolution of jumping performance, sexual dimorphism, and habitat in Anura

inferred← citeshttps://doi.org/10.3389/fevo.2023.1159037openalex-snapshot

Comparative transcriptome analysis revealed genes involved in the sexual size dimorphisms and expressed sequence tag-Simple Sequence Repeat loci validation in Odorrana graminea

inferred← citeshttps://doi.org/10.3390/ani15172566openalex-snapshot

Sexual Differences in Appendages of a Fossorial Narrow-Mouth Frog, Kaloula rugifera (Anura, Microhylidae)

inferred← citeshttps://doi.org/10.3390/biology10111081openalex-snapshot

Ecogeographical Adaptation Revisited: Morphological Variations in the Plateau Brown Frog along an Elevation Gradient on the Qinghai–Tibetan Plateau

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/10.35885/1684-7318-2024-3-304-322openalex-snapshot

Sexual dimorphism of the Pallas spadefoot toad (Pelobates vespertinus: Anura, Pelobatidae) metamorphs is reduced when tadpoles are developed in an overheated water body

inferred← citeshttps://doi.org/10.36253/a_h-11995openalex-snapshot

Age estimation and body size of the Parsley Frog, Pelodytes caucasicus Boulenger, 1896 from Lake Borçka Karagöl, Turkey

inferred← citeshttps://doi.org/10.36253/a_h-8955openalex-snapshot

Morphometric differentiation and sexual dimorphism in Limnomedusa macroglossa (Duméril & Bibron, 1841) (Anura: Alsodidae) from Uruguay

inferred← citeshttps://doi.org/10.3724/ahr.2095-0357.2023.0019openalex-snapshot

Redefinition of the Odorrana versabilis Group, with a New Species from China (Anura, Ranidae, Odorrana)

inferred← citeshttps://doi.org/10.3724/ahr.2095-0357.2024.0026openalex-snapshot

A New Species of the Genus Boulenophrys (Anura: Megophryidae: Megophryinae) from Zhuhai, Guangdong, China

inferred← citeshttps://doi.org/10.3897/herpetozoa.36.e95863openalex-snapshot

Trophic ecology of the Atlantic Forest endemic tree frog Boana bischoffi (Boulenger, 1887) (Anura, Hylidae)

inferred← citeshttps://doi.org/10.3897/vz.73.e98558openalex-snapshot

A new species of stream-living toad (Anura: Bufonidae: Bufo) from Guangdong, China

inferred← citeshttps://doi.org/10.6084/m9.figshare.16528768openalex-snapshot

Additional file 1 of Life history traits and reproductive ecology of North American chorus frogs of the genus Pseudacris (Hylidae)

inferred← citeshttps://doi.org/10.6084/m9.figshare.16528771openalex-snapshot

Additional file 2 of Life history traits and reproductive ecology of North American chorus frogs of the genus Pseudacris (Hylidae)

inferred← citeshttps://doi.org/10.6084/m9.figshare.16528774openalex-snapshot

Additional file 3 of Life history traits and reproductive ecology of North American chorus frogs of the genus Pseudacris (Hylidae)

inferred← citeshttps://doi.org/10.6084/m9.figshare.16528777openalex-snapshot

Additional file 4 of Life history traits and reproductive ecology of North American chorus frogs of the genus Pseudacris (Hylidae)

inferred← citeshttps://doi.org/10.7287/peerj.4050v0.1/reviews/1openalex-snapshot

Peer Review #1 of "Fitness implications of sex-specific catch-up growth in Nephila senegalensis, a spider with extreme reversed SSD (v0.1)"

inferred← citeshttps://doi.org/10.7287/peerj.4050v0.1/reviews/2openalex-snapshot

Peer Review #2 of "Fitness implications of sex-specific catch-up growth in Nephila senegalensis, a spider with extreme reversed SSD (v0.1)"

inferred← citeshttps://doi.org/10.7287/peerj.4050v0.2/reviews/2openalex-snapshot

Peer Review #2 of "Fitness implications of sex-specific catch-up growth in Nephila senegalensis, a spider with extreme reversed SSD (v0.2)"

inferred← citeshttps://doi.org/10.7717/peerj.15393openalex-snapshot

Integrative species delimitation helps to find the hidden diversity of the leaf-litter frog Ischnocnema manezinho (Garcia, 1996) (Anura, Brachycephalidae), endemic to the southern Atlantic Forest

inferred← citeshttps://doi.org/10.7717/peerj.4050openalex-snapshot

Fitness implications of sex-specific catch-up growth in Nephila senegalensis , a spider with extreme reversed SSD

inferred← citeshttps://doi.org/10.7717/peerj.5897openalex-snapshot

Amphibian life history in a temperate environment of the Mexican Plateau: dimorphism, phenology and trophic ecology of a hylid frog,Hyla eximia(=Dryophytes eximius)

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.