On the public citation graph

Only Half Right: Species with Female-Biased Sexual Size Dimorphism Consistently Break Rensch's Rule

https://doi.org/10.1371/journal.pone.0000897

0 signed · 189 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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.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.

inferreduses_data →https://doi.org/10.5281/zenodo.10723540zenodo-depositor-declared

inferredcites →https://doi.org/10.1006/bijl.1996.0020openalex-snapshot

Sexual size dimorphism and phylogeny in North American minnows

inferredcites →https://doi.org/10.1006/bijl.1996.0130openalex-snapshot

A phylogenetic analysis of the evolution of sexual dimorphism and mating systems in water striders (Hemiptera: Gerridae)

inferredcites →https://doi.org/10.1006/jhev.1996.0122openalex-snapshot

Body mass in comparative primatology

inferredcites →https://doi.org/10.1006/jhev.1998.0281openalex-snapshot

Statistics of sexual size dimorphism

inferredcites →https://doi.org/10.1007/bf01058194openalex-snapshot

Sexual dimorphism inAnastrepha suspensa (Loew) and other tephritid fruit flies (Diptera: Tephritidae): Possible roles of developmental rate, fecundity, and dispersal

inferredcites →https://doi.org/10.1016/j.zool.2006.04.003openalex-snapshot

Sexual size dimorphism in a Drosophila clade, the D. obscura group

inferredcites →https://doi.org/10.1016/s0022-5193(86)80090-xopenalex-snapshot

Sexual dimorphism in body size: Are larger species more dimorphic?

inferredcites →https://doi.org/10.1023/a:1019654100876openalex-snapshot

Scaling of Sexual Dimorphism in Body Mass: A Phylogenetic Analysis of Rensch's Rule in Primates

inferredcites →https://doi.org/10.1038/269797a0openalex-snapshot

Sexual dimorphism, socionomic sex ratio and body weight in primates

inferredcites →https://doi.org/10.1038/272652a0openalex-snapshot

Birds of the Western Palearctic

inferredcites →https://doi.org/10.1038/44766openalex-snapshot

Inferring the historical patterns of biological evolution

inferredcites →https://doi.org/10.1046/j.1095-8312.2002.00064.xopenalex-snapshot

Body size, male combat and the evolution of sexual dimorphism in eublepharid geckos (Squamata: Eublepharidae)

inferredcites →https://doi.org/10.1046/j.1095-8312.2003.00252.xopenalex-snapshot

Female-biased sexual size dimorphism in tinamous: a comparative test fails to support Rensch's rule

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

Sexual selection explains Rensch's rule of size dimorphism in shorebirds

inferredcites →https://doi.org/10.1073/pnas.0602994103openalex-snapshot

The allometry of ornaments and weapons

inferredcites →https://doi.org/10.1073/pnas.92.23.10614openalex-snapshot

Delayed male maturity is a cost of producing large sperm in Drosophila.

inferredcites →https://doi.org/10.1080/01621459.1994.10476871openalex-snapshot

Simulation-Extrapolation Estimation in Parametric Measurement Error Models

inferredcites →https://doi.org/10.1080/10635159950127330openalex-snapshot

The Phylogenetic Basis of Sexual Size Dimorphism in Orb-Weaving Spiders (Araneae, Orbiculariae)

inferredcites →https://doi.org/10.1080/15627020.2003.11657210openalex-snapshot

Evolutionary Ecology of Birds: Life Histories, Mating Systems and Extinction

inferredcites →https://doi.org/10.1086/285663openalex-snapshot

Sexual Selection and the Evolution of Allometry for Sexual Size Dimorphism in the Water Strider, Aquarius remigis

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/10.1086/303406openalex-snapshot

Rensch’s Rule Crosses the Line: Convergent Allometry of Sexual Size Dimorphism in Hummingbirds and Flower Mites

inferredcites →https://doi.org/10.1086/343873openalex-snapshot

Phylogenetic Analysis and Comparative Data: A Test and Review of Evidence

inferredcites →https://doi.org/10.1086/444600openalex-snapshot

Allometry for Sexual Size Dimorphism: Testing Two Hypotheses for Rensch’s Rule in the Water Strider Aquarius remigis

inferredcites →https://doi.org/10.1086/505763openalex-snapshot

Ecology Predicts Large‐Scale Patterns of Phylogenetic Diversification in Birds

inferredcites →https://doi.org/10.1086/510597openalex-snapshot

Proximate Causes of Rensch’s Rule: Does Sexual Size Dimorphism in Arthropods Result from Sex Differences in Development Time?

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/9780199208784.003.0004openalex-snapshot

Sexual size dimorphism in birds

inferredcites →https://doi.org/10.1111/j.0014-3820.2001.tb00659.xopenalex-snapshot

PHYLOGENETIC ANALYSIS OF SEXUAL DIMORPHISM AND EYE-SPAN ALLOMETRY IN STALK-EYED FLIES (DIOPSIDAE)

inferredcites →https://doi.org/10.1111/j.1095-8312.2002.tb02089.xopenalex-snapshot

Body size, male combat and the evolution of sexual dimorphism in eublepharid geckos (Squamata: Eublepharidae)

inferredcites →https://doi.org/10.1111/j.1095-8312.2005.00549.xopenalex-snapshot

Sexual size dimorphism and sex ratios in dragonflies (Odonata)

inferredcites →https://doi.org/10.1111/j.1365-2656.2006.01141.xopenalex-snapshot

Why do we still use stepwise modelling in ecology and behaviour?

inferredcites →https://doi.org/10.1111/j.1558-5646.1992.tb01158.xopenalex-snapshot

SEXUAL DIMORPHISM, MATING SYSTEM AND BODY SIZE IN NEW WORLD BLACKBIRDS (ICTERINAE)

inferredcites →https://doi.org/10.1111/j.1558-5646.1996.tb03927.xopenalex-snapshot

SEXUAL SELECTION AND THE EVOLUTION OF SEXUAL SIZE DIMORPHISM IN THE WATER STRIDER,AQUARIUS REMIGIS

inferredcites →https://doi.org/10.1139/z03-194openalex-snapshot

Body size, sexual size dimorphism, and Rensch's rule in adult hydropsychid caddisflies (Trichoptera: Hydropsychidae)

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/10.1201/9781003449973openalex-snapshot

Linear Models with R

inferredcites →https://doi.org/10.1371/journal.pbio.0040208openalex-snapshot

Global Patterns of Geographic Range Size in Birds

inferredcites →https://doi.org/10.1890/03-9000openalex-snapshot

TOWARD A METABOLIC THEORY OF ECOLOGY

inferredcites →https://doi.org/10.2307/3078855openalex-snapshot

Phylogenetic Analysis and Comparative Data: A Test and Review of Evidence

inferredcites →https://doi.org/10.2307/3473067openalex-snapshot

Allometry for Sexual Size Dimorphism: Testing Two Hypotheses for Rensch's Rule in the Water Strider Aquarius remigis

inferredcites →https://doi.org/10.2307/4089462openalex-snapshot

Evolution of Reversed Sexual Size Dimorphism in Skuas and Jaegers

inferredcites →https://doi.org/10.2307/j.ctt1xp3v3ropenalex-snapshot

Phylogeny and Classification of the Birds

inferredcites →https://doi.org/10.32614/r.manualsopenalex-snapshot

R: A Language and Environment for Statistical Computing

inferredcites →https://doi.org/10.5281/zenodo.16292283openalex-snapshot

The Evolution of Reversed Sexual Dimorphism in Owls: An Empirical Analysis of Possible Selective Factors

inferredcites →https://doi.org/10.5860/choice.28-5665openalex-snapshot

Phylogeny and classification of birds: a study in molecular evolution

inferredcites →https://doi.org/10.5860/choice.30-4983openalex-snapshot

The evolution of life histories: theory and analysis

inferredcites →https://doi.org/10.7312/rens91062openalex-snapshot

Evolution Above the Species Level

What points at this work

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

inferred← citeshttps://doi.org/10.1002/ajpa.21541openalex-snapshot

Rensch's rule, Bergmann's effect and adult sexual dimorphism in wild monogamous owl monkeys (Aotus azarai) of Argentina

inferred← citeshttps://doi.org/10.1002/ajpa.24836openalex-snapshot

Morphological variability or inter‐observer bias? A methodological toolkit to improve data quality of multi‐researcher datasets for the analysis of morphological variation

inferred← citeshttps://doi.org/10.1002/ece3.11163openalex-snapshot

The origins and drivers of sexual size dimorphism in sharks

inferred← citeshttps://doi.org/10.1002/ece3.2480openalex-snapshot

Sexual size dimorphism in musteloids: An anomalous allometric pattern is explained by feeding ecology

inferred← citeshttps://doi.org/10.1002/ece3.2572openalex-snapshot

The interplay between natural and sexual selection in the evolution of sexual size dimorphism inSceloporuslizards (Squamata: Phrynosomatidae)

inferred← citeshttps://doi.org/10.1002/ece3.2658openalex-snapshot

Latitudinal variation in sexual dimorphism in life‐history traits of a freshwater fish

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/ece3.4935openalex-snapshot

Patterns of sexual size dimorphism in stingless bees: Testing Rensch’s rule and potential causes in highly eusocial bees (Hymenoptera: Apidae, Meliponini)

inferred← citeshttps://doi.org/10.1002/ece3.5492openalex-snapshot

Female‐biased gape and body‐size dimorphism in the New World watersnakes (tribe: Thamnophiini) oppose predictions from Rensch's rule

inferred← citeshttps://doi.org/10.1002/ece3.65openalex-snapshot

Macroevolutionary patterns of bumblebee body size: detecting the interplay between natural and sexual selection

inferred← citeshttps://doi.org/10.1002/ece3.70188openalex-snapshot

Annual temperature, body size, and sexual size dimorphism in the evolution of Pyrgomorphidae

inferred← citeshttps://doi.org/10.1002/ece3.71501openalex-snapshot

Sex on the Beach: Sexual Size Dimorphism Among Aquatic Bugs (Nepomorpha) Inhabiting Different Habitats

inferred← citeshttps://doi.org/10.1002/ece3.71858openalex-snapshot

Sexual Size Dimorphism in Rays and Skates (Elasmobranchii: Batoidea)

inferred← citeshttps://doi.org/10.1002/ece3.73825openalex-snapshot

Variations in Sexual Size Dimorphism in Two Anurans Along an Urbanization Gradient in Shanghai: Assessment of Rensch's Rule

inferred← citeshttps://doi.org/10.1002/ece3.74202openalex-snapshot

Sexual Dimorphism as a Potential Driver of Trophic Specialisation in a Sedentary Synanthropic Bat Species

inferred← citeshttps://doi.org/10.1002/ece3.8070openalex-snapshot

An evolutionary explanation of female‐biased sexual size dimorphism in North Sea plaice, Pleuronectes platessa L.

inferred← citeshttps://doi.org/10.1002/ece3.9907openalex-snapshot

Sexual size and shape dimorphism, and allometric scaling in the pupal and adult traits of Eristalis tenax

inferred← citeshttps://doi.org/10.1007/978-3-030-88800-8_11-1openalex-snapshot

Trait Variation in American Marsupials Based on Biological Rules

inferred← citeshttps://doi.org/10.1007/978-3-032-23194-9_2openalex-snapshot

Allometry and the Evolution of Sexual Size Dimorphism in Scorpions: Insights from Neotropical Species

inferred← citeshttps://doi.org/10.1007/978-3-319-41324-2_8openalex-snapshot

Evolutionary Pathways Maintaining Extreme Female-Biased Sexual Size Dimorphism: Convergent Spider Cases Defy Common Patterns

inferred← citeshttps://doi.org/10.1007/s00040-016-0491-1openalex-snapshot

Variable patterns of intraspecific sexual size dimorphism and allometry in three species of eusocial corbiculate bees

inferred← citeshttps://doi.org/10.1007/s00114-015-1264-9openalex-snapshot

Strong support for Rensch’s rule in an American clade of lizards (Teiidae and Gymnophtalmidae) and a paradox of the largest tejus

inferred← citeshttps://doi.org/10.1007/s00265-013-1498-5openalex-snapshot

Evolution of mating systems and sexual size dimorphism in North American cyprinids

inferred← citeshttps://doi.org/10.1007/s00435-011-0143-yopenalex-snapshot

Sexual dimorphism in the skull geometry of newt species of Ichthyosaura, Triturus and Lissotriton (Salamandridae, Caudata, Amphibia)

inferred← citeshttps://doi.org/10.1007/s00436-022-07437-3openalex-snapshot

Relationship between body size and sexual size dimorphism in syringophilid quill mites

inferred← citeshttps://doi.org/10.1007/s10682-010-9354-9openalex-snapshot

Patterns of sexual size dimorphism in cattle breeds support Rensch’s rule

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/s10750-022-04844-6openalex-snapshot

Sexual size dimorphism of two common European percid fish: linkage with spatial distribution and diet

inferred← citeshttps://doi.org/10.1007/s11284-013-1090-5openalex-snapshot

Altitudinal variation in body size in Abacarus panticis Keifer (Acari: Eriophyidae)

inferred← citeshttps://doi.org/10.1007/s11692-012-9199-yopenalex-snapshot

Phylogenetic Patterns of Sexual Size Dimorphism in Turtles and Their Implications for Rensch’s Rule

inferred← citeshttps://doi.org/10.1007/s11692-012-9212-5openalex-snapshot

Evolution of Sexual Size Dimorphism in a Frog Obeys the Inverse of Rensch’s Rule

inferred← citeshttps://doi.org/10.1007/s11692-017-9416-9openalex-snapshot

Latitudinal Influence on the Sexual Dimorphism of the Marine Fish Bathygobius soporator (Gobiidae: Teleostei)

inferred← citeshttps://doi.org/10.1007/s11692-019-09482-wopenalex-snapshot

The Shape of Weaver: Investigating Shape Disparity in Orb-Weaving Spiders (Araneae, Araneidae) Using Geometric Morphometrics

inferred← citeshttps://doi.org/10.1007/s13744-014-0196-yopenalex-snapshot

Allometry for Sexual Size Dimorphism in Stoneflies Defies the Rensch’s Rule

inferred← citeshttps://doi.org/10.1007/s42991-022-00239-1openalex-snapshot

Sexual dimorphism in toothed whales (Odontoceti) follows Rensch’s rule

inferred← citeshttps://doi.org/10.1016/b978-0-12-800049-6.00157-8openalex-snapshot

Sexual Dimorphism

inferred← citeshttps://doi.org/10.1016/b978-0-443-15750-9.00008-2openalex-snapshot

Sexual Dimorphism

inferred← citeshttps://doi.org/10.1016/j.anireprosci.2012.02.007openalex-snapshot

Mammalian sexual dimorphism

inferred← citeshttps://doi.org/10.1016/j.ijpara.2018.05.006openalex-snapshot

Sexual size dimorphism and sex ratio in arthropod ectoparasites: contrasting patterns at different hierarchical scales

inferred← citeshttps://doi.org/10.1016/j.jcz.2020.01.003openalex-snapshot

Sexual dimorphism and variability of craniomandibular morphology in the Japanese giant flying squirrel, Petaurista leucogenys (Rodentia: Sciuridae)

inferred← citeshttps://doi.org/10.1016/j.mambio.2014.11.008openalex-snapshot

A re-assessment of Rensch's rule in tuco-tucos (Rodentia: Ctenomyidae: Ctenomys) using a phylogenetic approach

inferred← citeshttps://doi.org/10.1038/s41598-018-21077-7openalex-snapshot

Patterns of sexual size dimorphism in horseshoe bats: Testing Rensch’s rule and potential causes

inferred← citeshttps://doi.org/10.1038/s41598-019-44370-5openalex-snapshot

Rensch’s rule in avian lice: contradictory allometric trends for sexual size dimorphism

inferred← citeshttps://doi.org/10.1038/s41598-022-22181-5openalex-snapshot

Ecological and evolutionary trends of body size in Pristimantis frogs, the world's most diverse vertebrate genus

inferred← citeshttps://doi.org/10.1080/00222933.2014.886343openalex-snapshot

Butterflies (Lepidoptera: Papilionoidea) of Mount Kilimanjaro: family Pieridae, subfamily Pierinae

inferred← citeshttps://doi.org/10.1080/01647954.2017.1370012openalex-snapshot

Postembryonic development of Sejus togatus CL Koch, 1836 (Parasitiformes: Mesostigmata: Sejida) with notes on moulting behaviour

inferred← citeshttps://doi.org/10.1086/662175openalex-snapshot

Allometry of Sexual Size Dimorphism in Dioecious Plants: Do Plants Obey Rensch’s Rule?

inferred← citeshttps://doi.org/10.1086/673282openalex-snapshot

Correlated Evolution of Allometry and Sexual Dimorphism across Higher Taxa

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/aesa/101.5.802openalex-snapshot

Rensch's Rule in Dichroplus pratensis: a Reply to Wolak

inferred← citeshttps://doi.org/10.1093/biolinnean/blad090openalex-snapshot

On the evolution of body size and of sexual dimorphism in corbiculate bees

inferred← citeshttps://doi.org/10.1093/cz/zoab070openalex-snapshot

Sexual dimorphism in cranial shape and size in geomyoid rodents: multivariate and evolutionary perspectives

inferred← citeshttps://doi.org/10.1093/iob/obae025openalex-snapshot

Sharks Violate Rensch's Rule for Sexual Size Dimorphism

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

Macroevolutionary Patterns of Sexual Size Dimorphism Among African Tree Frogs (Family: Hyperoliidae)

inferred← citeshttps://doi.org/10.1093/jmammal/gyv120openalex-snapshot

Patterns of secondary sexual size dimorphism in New World Myotis and a test of Rensch’s rule

inferred← citeshttps://doi.org/10.1093/obo/9780199941728-0110openalex-snapshot

Sexual Size Dimorphism

inferred← citeshttps://doi.org/10.1093/sysbio/syy082openalex-snapshot

Golden Orbweavers Ignore Biological Rules: Phylogenomic and Comparative Analyses Unravel a Complex Evolution of Sexual Size Dimorphism

inferred← citeshttps://doi.org/10.1098/rsbl.2024.0301openalex-snapshot

Patterns of sexual dimorphism in the armoured tardigrades

inferred← citeshttps://doi.org/10.1098/rsos.170453openalex-snapshot

Rensching cats and dogs: feeding ecology and fecundity trends explain variation in the allometry of sexual size dimorphism

inferred← citeshttps://doi.org/10.1098/rspb.2014.0739openalex-snapshot

Macroevolutionary patterns of sexual size dimorphism in copepods

inferred← citeshttps://doi.org/10.1098/rspb.2019.2640openalex-snapshot

Selection for increased male size predicts variation in sexual size dimorphism among fish species

inferred← citeshttps://doi.org/10.1111/1365-2435.12172openalex-snapshot

Sexual size dimorphism requires a corresponding sex difference in development time: a meta‐analysis in insects

inferred← citeshttps://doi.org/10.1111/1744-7917.12272openalex-snapshot

Lack of support for Rensch's rule in an intraspecific test using red flour beetle (Tribolium castaneum) populations

inferred← citeshttps://doi.org/10.1111/1749-4877.12896openalex-snapshot

Nephila spider male aggregation: preference for optimal female size and web clustering

inferred← citeshttps://doi.org/10.1111/afe.12399openalex-snapshot

Is body size a good indicator of fecundity in the genus Thaumetopoea ? A story told by two intrageneric Mediterranean forest defoliators

inferred← citeshttps://doi.org/10.1111/azo.12183openalex-snapshot

Intraspecific variation in body size and sexual size dimorphism, and a test of Rensch's rule in bats

inferred← citeshttps://doi.org/10.1111/bij.12848openalex-snapshot

Sexual size dimorphism and Rensch's rule in Canidae

inferred← citeshttps://doi.org/10.1111/ecog.03382openalex-snapshot

Interrelations of global macroecological patterns in wing and thorax size, sexual size dimorphism, and range size of the Drosophilidae

inferred← citeshttps://doi.org/10.1111/evo.13799openalex-snapshot

Sexual dimorphism explains residual variance around the survival‐reproduction tradeoff in lizards: Implications for sexual conflict over life‐history evolution*

inferred← citeshttps://doi.org/10.1111/evo.14642openalex-snapshot

Influence of microhabitat, fecundity, and parental care on the evolution of sexual size dimorphism in Caribbean Eleutherodactylus frogs

inferred← citeshttps://doi.org/10.1111/j.1095-8312.2010.01430.xopenalex-snapshot

A test of Rensch's rule in varanid lizards

inferred← citeshttps://doi.org/10.1111/j.1095-8312.2011.01633.xopenalex-snapshot

Which proximate factor determines sexual size dimorphism in tiger snakes?

inferred← citeshttps://doi.org/10.1111/j.1095-8312.2012.02015.xopenalex-snapshot

Patterns of sexual size dimorphism in Chelonia

inferred← citeshttps://doi.org/10.1111/j.1365-2656.2010.01665.xopenalex-snapshot

Rensch’s rule inverted – female‐driven gigantism in nine‐spined stickleback Pungitius pungitius

inferred← citeshttps://doi.org/10.1111/j.1420-9101.2010.01933.xopenalex-snapshot

Macroevolutionary pattern of sexual size dimorphism in geckos corresponds to intraspecific temperature‐induced variation

inferred← citeshttps://doi.org/10.1111/j.1420-9101.2010.02126.xopenalex-snapshot

Domestic chickens defy Rensch’s rule: sexual size dimorphism in chicken breeds

inferred← citeshttps://doi.org/10.1111/j.1439-0469.2008.00479.xopenalex-snapshot

Sexual size and shape evolution in European newts (Amphibia: Caudata: Salamandridae) on the Balkan Peninsula

inferred← citeshttps://doi.org/10.1111/jbi.13680openalex-snapshot

Assessing Rensch’s rule in a newt: Roles of primary productivity and conspecific density in interpopulation variation of sexual size dimorphism

inferred← citeshttps://doi.org/10.1111/jeb.12349openalex-snapshot

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

inferred← citeshttps://doi.org/10.1111/jeb.13131openalex-snapshot

Ecological drivers of body size evolution and sexual size dimorphism in short‐horned grasshoppers (Orthoptera: Acrididae)

inferred← citeshttps://doi.org/10.1111/jeb.14172openalex-snapshot

Extra‐pair paternity and sexual dimorphism in birds

inferred← citeshttps://doi.org/10.1111/jfb.13675openalex-snapshot

Female‐biased dimorphism in size and age at maturity is reduced at higher latitudes in lake whitefish Coregonus clupeaformis

inferred← citeshttps://doi.org/10.1111/jfb.14145openalex-snapshot

Sexually selected traits are larger and more variable in male than female beach‐spawning capelin, Mallotus villosus

inferred← citeshttps://doi.org/10.1111/jfb.14647openalex-snapshot

The growth and age structure of Chilean jack mackerel ( Trachurus murphyi ) following its influx to New Zealand waters

inferred← citeshttps://doi.org/10.1111/jzo.12042openalex-snapshot

Elevation‐related variation in life history traits among P hrynocephalus lineages on the T ibetan P lateau: do they follow typical squamate ecogeographic patterns?

inferred← citeshttps://doi.org/10.1111/jzo.12137openalex-snapshot

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

inferred← citeshttps://doi.org/10.1111/jzo.12243openalex-snapshot

Large‐scale variation of size‐ and age‐related life‐history traits in the common frog: a sensitive test case for macroecological rules

inferred← citeshttps://doi.org/10.1111/maec.12534openalex-snapshot

The Cabo Frio upwelling overrides geographical patterns in the population dynamics of the shrimp Artemesia longinaris Spence Bate, 1888 (Decapoda: Penaeidae)

inferred← citeshttps://doi.org/10.1111/maec.70041openalex-snapshot

Ecological Process Explains the Rensch's Rule in Penaeidae (Decapoda, Dendrobranchiata)

inferred← citeshttps://doi.org/10.1134/s1062359023070300openalex-snapshot

Sexual Dimorphism in the Ontogeny of the Black Forest–Steppe Adder (Pelias berus nikolskii (Vedmederja, Grubant et Rudaeva 1986), Serpentes, Viperidae) from Voronezh Oblast, Based on Traditional Measurements

inferred← citeshttps://doi.org/10.1139/cjz-2018-0063openalex-snapshot

Testing Rensch’s rule in Acanthoscelides macrophthalmus, a seed-feeding beetle infesting Leucaena leucocephala plants

inferred← citeshttps://doi.org/10.1139/z08-103openalex-snapshot

Plasticity in sexual size dimorphism and Rensch’s rule in Mediterranean blennies (Blenniidae)

inferred← citeshttps://doi.org/10.1146/annurev-ento-011019-025032openalex-snapshot

Sexual Size Dimorphism: Evolution and Perils of Extreme Phenotypes in Spiders

inferred← citeshttps://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

inferred← citeshttps://doi.org/10.1155/2012/167420openalex-snapshot

Abiotic Factors and Insect Abundance

inferred← citeshttps://doi.org/10.1155/2012/863947openalex-snapshot

Effects of Abiotic Factors on the Geographic Distribution of Body Size Variation and Chromosomal Polymorphisms in Two Neotropical Grasshopper Species (Dichroplus: Melanoplinae: Acrididae)

inferred← citeshttps://doi.org/10.1163/15707563-00002431openalex-snapshot

Pattern of sexual size dimorphism supports the inverse of Rensch’s rule in two frog species

inferred← citeshttps://doi.org/10.1163/15707563-bja10076openalex-snapshot

Nest site selection and breeding ecology of the red-billed blue magpie Urocissa erythrorhyncha in central China

inferred← citeshttps://doi.org/10.1177/17581559251331754openalex-snapshot

Comparative analysis of weight in male and female sihek ( Todiramphus cinnamominus) chicks at Brookfield Zoo Chicago

inferred← citeshttps://doi.org/10.1186/1742-9994-10-10openalex-snapshot

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

inferred← citeshttps://doi.org/10.1186/1742-9994-10-27openalex-snapshot

Sexual size dimorphism in ground squirrels (Rodentia: Sciuridae: Marmotini) does not correlate with body size and sociality

inferred← citeshttps://doi.org/10.12976/jib/2013.1.12openalex-snapshot

Rensch's rule is not verified in melanopline grasshoppers (Acrididae)

inferred← citeshttps://doi.org/10.1371/journal.pone.0046125openalex-snapshot

Allometry of Sexual Size Dimorphism in Domestic Dog

inferred← citeshttps://doi.org/10.1371/journal.pone.0086085openalex-snapshot

A Test of Rensch’s Rule in Greater Horseshoe Bat (Rhinolophus ferrumequinum) with Female-Biased Sexual Size Dimorphism

inferred← citeshttps://doi.org/10.1371/journal.pone.0145248openalex-snapshot

Body Size Adaptations to Altitudinal Climatic Variation in Neotropical Grasshoppers of the Genus Sphenarium (Orthoptera: Pyrgomorphidae)

inferred← citeshttps://doi.org/10.1371/journal.pone.0215317openalex-snapshot

Ontogeny of sexual size dimorphism revisited: Females grow for a longer time and also faster

inferred← citeshttps://doi.org/10.1556/1777.2024.00027openalex-snapshot

Among-population variation in sexual size dimorphism of Nepa cinerea (Heteroptera: Nepomorpha)

inferred← citeshttps://doi.org/10.1603/0013-8746(2008)101[802:rridpa]2.0.co;2openalex-snapshot

Rensch’s Rule in Dichroplus pratensis: A Reply to Wolak

inferred← citeshttps://doi.org/10.17352/gjz.000010openalex-snapshot

Centrobolus silvanus dimorphism based on tergite width

inferred← citeshttps://doi.org/10.18699/vj17.263openalex-snapshot

Cats and dogs cross the line: domestic breeds follow Rensch’s rule, their wild relatives do not

inferred← citeshttps://doi.org/10.20431/2454-941x.0403003openalex-snapshot

Centrobolus dubius (Schubart, 1966) Monomorphism

inferred← citeshttps://doi.org/10.21203/rs.3.rs-9898794/v1openalex-snapshot

Sexual dimorphism in the canines and mandibles of the Icelandic Arctic fox

inferred← citeshttps://doi.org/10.22271/j.ento.2017.v5.i2u.04openalex-snapshot

Relative sexual size dimorphism in Centrobolus digrammus (Pocock) compared to 18 congenerics

inferred← citeshttps://doi.org/10.22271/j.ento.2017.v5.i3b.01openalex-snapshot

Relative sexual size dimorphism in Centrobolus fulgidus (Lawrence) compared to 18 congenerics

inferred← citeshttps://doi.org/10.22271/j.ento.2017.v5.i3c.07openalex-snapshot

Relative sexual size dimorphism Centrobolus ruber (Attems) compared to 18 congenerics

inferred← citeshttps://doi.org/10.22271/j.ento.2018.v6.i1b.03openalex-snapshot

Allometry for sexual dimorphism in millipedes (Diplopoda)

inferred← citeshttps://doi.org/10.22271/j.ento.2018.v6.i1i.03openalex-snapshot

Sexual dimorphism in pill millipedes (Diplopoda)

inferred← citeshttps://doi.org/10.22271/j.ento.2018.v6.i1v.07openalex-snapshot

Sexual size dimorphism and the rejection of Rensch’s rule in Diplopoda (Arthropoda)

inferred← citeshttps://doi.org/10.22271/j.ento.2018.v6.i3.9.09openalex-snapshot

Trigoniulid size dimorphism breaks Rensch

inferred← citeshttps://doi.org/10.22271/j.ento.2018.v6.i4.13.16openalex-snapshot

Centrobolus anulatus (Attems, 1934) reversed sexual size dimorphism

inferred← citeshttps://doi.org/10.22271/j.ento.2018.v6.i6.3.05openalex-snapshot

Centrobolus sagatinus sexual size dimorphism based on differences in horizontal tergite widths

inferred← citeshttps://doi.org/10.22271/j.ento.2018.v6.i6.3.07openalex-snapshot

Allometry in Centrobolus

inferred← citeshttps://doi.org/10.22271/j.ento.2019.v7.i2.9.07openalex-snapshot

Lawrence’s red millipede Centrobolus lawrencei shows length-based variability and size dimorphism

inferred← citeshttps://doi.org/10.2298/abs160229060iopenalex-snapshot

Sexual dimorphism in Apfelbeckia insculpta (L. Koch, 1867) (Myriapoda: Diplopoda: Callipodida)

inferred← citeshttps://doi.org/10.26757/pjsb2019a13011openalex-snapshot

Sexual dimorphism of invasive knifefish (Chitala ornata) in Laguna de bay, Philippines

inferred← citeshttps://doi.org/10.30550/j.azl/2199openalex-snapshot

Incumplimiento del postulado de Rensch en páridos (Paridae: Passeriformes)

inferred← citeshttps://doi.org/10.33545/27080013.2022.v3.i1a.57openalex-snapshot

Does sexual size dimorphism vary with female size in forest millipedes Centrobolus Cook, 1897?

inferred← citeshttps://doi.org/10.3389/fcell.2021.743722openalex-snapshot

Integration of Transcriptome and Methylome Highlights the Roles of Cell Cycle and Hippo Signaling Pathway in Flatfish Sexual Size Dimorphism

inferred← citeshttps://doi.org/10.3389/fevo.2021.638754openalex-snapshot

Effects of Sex and Breeding Status on Skull Morphology in Cooperatively Breeding Ansell’s Mole-Rats and an Appraisal of Sexual Dimorphism in the Bathyergidae

inferred← citeshttps://doi.org/10.3389/fevo.2023.1155261openalex-snapshot

Island and Rensch’s rules do not apply to cave vs. surface populations of Asellus aquaticus

inferred← citeshttps://doi.org/10.3390/d10030085openalex-snapshot

High Duty Cycle Echolocation May Constrain the Evolution of Diversity within Horseshoe Bats (Family: Rhinolophidae)

inferred← citeshttps://doi.org/10.3390/insects16121249openalex-snapshot

Sexual Size Dimorphism Depends Drastically on Environment: The Case Study in Ground Beetles

inferred← citeshttps://doi.org/10.64898/2026.06.26.734866openalex-snapshot

Doublesex- mediated regulation of insulin signaling drives sex-specific body growth

inferred← citeshttps://doi.org/10.7287/peerj.2914v0.1/reviews/1openalex-snapshot

Peer Review #1 of "Allometry of sexual size dimorphism in turtles: a comparison of mass and length data (v0.1)"

inferred← citeshttps://doi.org/10.7287/peerj.2914v0.1/reviews/2openalex-snapshot

Peer Review #2 of "Allometry of sexual size dimorphism in turtles: a comparison of mass and length data (v0.1)"

inferred← citeshttps://doi.org/10.7287/peerj.2914v0.1/reviews/3openalex-snapshot

Peer Review #3 of "Allometry of sexual size dimorphism in turtles: a comparison of mass and length data (v0.1)"

inferred← citeshttps://doi.org/10.7287/peerj.2914v0.2/reviews/1openalex-snapshot

Peer Review #1 of "Allometry of sexual size dimorphism in turtles: a comparison of mass and length data (v0.2)"

inferred← citeshttps://doi.org/10.7287/peerj.2914v0.2/reviews/3openalex-snapshot

Peer Review #3 of "Allometry of sexual size dimorphism in turtles: a comparison of mass and length data (v0.2)"

inferred← citeshttps://doi.org/10.7717/peerj.2914openalex-snapshot

Allometry of sexual size dimorphism in turtles: a comparison of mass and length data

inferred← citeshttps://doi.org/10.7818/ecos.2014.23-1.05openalex-snapshot

A phylogenetic approach to the study of sexual size dimorphism in Felidae and an assessment of Rensch´s rule.

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.