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Is Diet Quality an Overlooked Mechanism for Bergmann’s Rule?
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/bies.20456openalex-snapshot
A role for genetic accommodation in evolution?
inferredcites →https://doi.org/10.1007/bf00320811openalex-snapshot
Influence of aphid size, age and behaviour on host choice by the parasitoid wasp Ephedrus californicus: a test of host-size models
inferredcites →https://doi.org/10.1007/bf00341355openalex-snapshot
Geographical and latitudinal variation in growth patterns and adult body size of Swedish moose (Alces alces)
inferredcites →https://doi.org/10.1007/s00442-006-0364-9openalex-snapshot
Geographic variation in body size: the effects of ambient temperature and precipitation
inferredcites →https://doi.org/10.1007/s00442-006-0519-8openalex-snapshot
Environmental phenology and geographical gradients in moose body mass
inferredcites →https://doi.org/10.1007/s00442-006-0609-7openalex-snapshot
Nutrients stimulate leaf breakdown rates and detritivore biomass: bottom-up effects via heterotrophic pathways
inferredcites →https://doi.org/10.1007/s12237-007-9026-3openalex-snapshot
Grasshopper (Orthoptera: Tettigoniidae) Species Composition and Size Across Latitude in Atlantic Coast Salt Marshes
inferredcites →https://doi.org/10.1016/0022-0981(80)90179-3openalex-snapshot
Studies on the nutrition and feeding preferences of Aplysia: Development of an artificial diet
inferredcites →https://doi.org/10.1016/s0065-2504(08)60212-3openalex-snapshot
Temperature and Organism Size—A Biological Law for Ectotherms?
inferredcites →https://doi.org/10.1038/nature02403openalex-snapshot
The worldwide leaf economics spectrum
inferredcites →https://doi.org/10.1073/pnas.0501844102openalex-snapshot
Developmental plasticity and the origin of species differences
inferredcites →https://doi.org/10.1086/285038openalex-snapshot
Experimental Aquatic Food Webs: Interactions between Two Predators and Two Prey
inferredcites →https://doi.org/10.1086/374346openalex-snapshot
Bergmann’s Rule and Body Size in Mammals
inferredcites →https://doi.org/10.1086/377187openalex-snapshot
The Temperature‐Size Rule in Ectotherms: Simple Evolutionary Explanations May Not Be General
inferredcites →https://doi.org/10.1086/425222openalex-snapshot
Bergmann’s Clines in Ectotherms: Illustrating a Life‐History Perspective with Sceloporine Lizards
inferredcites →https://doi.org/10.1086/498277openalex-snapshot
Imbalance of Predator and Prey Armament: Geographic Clines in Phenotypic Interface and Natural Selection
inferredcites →https://doi.org/10.1086/501029openalex-snapshot
The Temperature‐Size Rule in Ectotherms: May a General Explanation Exist after All?
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/10.1093/icb/44.6.413openalex-snapshot
Bergmann and Converse Bergmann Latitudinal Clines in Arthropods: Two Ends of a Continuum?
inferredcites →https://doi.org/10.1111/j.0014-3820.2006.tb01838.xopenalex-snapshot
WHEN RENSCH MEETS BERGMANN: DOES SEXUAL SIZE DIMORPHISM CHANGE SYSTEMATICALLY WITH LATITUDE?
inferredcites →https://doi.org/10.1111/j.1096-3642.1974.tb00793.xopenalex-snapshot
Aplysiid species from East Africa with notes on the Indian Ocean Aplysiomorpha (Gastropoda: Opisthobranchia)
inferredcites →https://doi.org/10.1111/j.1365-2311.2003.00554.xopenalex-snapshot
Bergmann's rule in larval ant lions: testing the starvation resistance hypothesis
inferredcites →https://doi.org/10.1111/j.1461-0248.2006.00928.xopenalex-snapshot
Ecotypic variation in the context of global climate change: revisiting the rules
inferredcites →https://doi.org/10.1111/j.1558-5646.1956.tb02836.xopenalex-snapshot
GEOGRAPHICAL CHARACTER GRADIENTS AND CLIMATIC ADAPTATION
inferredcites →https://doi.org/10.1111/j.1558-5646.1973.tb00673.xopenalex-snapshot
GENETIC DIVERGENCE IN BODY SIZE AMONG EXPERIMENTAL POPULATIONS OFDROSOPHILA PSEUDOOBSCURAKEPT AT DIFFERENT TEMPERATURES
inferredcites →https://doi.org/10.1111/j.1558-5646.1994.tb05311.xopenalex-snapshot
EVOLUTION AND DEVELOPMENT OF BODY SIZE AND CELL SIZE INDROSOPHILA MELANOGASTERIN RESPONSE TO TEMPERATURE
inferredcites →https://doi.org/10.1111/j.1558-5646.1996.tb02366.xopenalex-snapshot
BERGMANN SIZE CLINES: A SIMPLE EXPLANATION FOR THEIR OCCURRENCE IN ECTOTHERMS
inferredcites →https://doi.org/10.1111/j.1558-5646.1996.tb03621.xopenalex-snapshot
THERMAL EVOLUTION OF EGG SIZE INDROSOPHILA MELANOGASTER
inferredcites →https://doi.org/10.1111/j.1558-5646.1997.tb02453.xopenalex-snapshot
ECTOTHERMS FOLLOW THE CONVERSE TO BERGMANN'S RULE
inferredcites →https://doi.org/10.1111/j.1558-5646.2008.00467.xopenalex-snapshot
SELECTION DOES NOT FAVOR LARGER BODY SIZE AT LOWER TEMPERATURE IN A SEED-FEEDING BEETLE
inferredcites →https://doi.org/10.1126/science.258.5086.1348openalex-snapshot
Predator-Induced Phenotypical Change in Body Morphology in Crucian Carp
inferredcites →https://doi.org/10.1126/science.287.5451.308openalex-snapshot
Rapid Evolution of a Geographic Cline in Size in an Introduced Fly
inferredcites →https://doi.org/10.1890/0012-9658(2001)082[1344:ldippi]2.0.co;2openalex-snapshot
LATITUDINAL DIFFERENCES IN PLANT PALATABILITY IN ATLANTIC COAST SALT MARSHES
inferredcites →https://doi.org/10.1890/0012-9658(2002)083[3369:lvipos]2.0.co;2openalex-snapshot
LATITUDINAL VARIATION IN PALATABILITY OF SALT-MARSH PLANTS: WHICH TRAITS ARE RESPONSIBLE?
inferredcites →https://doi.org/10.1890/0012-9658(2003)084[1032:prarso]2.0.co;2openalex-snapshot
PREDATION RISK AFFECTS RELATIVE STRENGTH OF TOP-DOWN AND BOTTOM-UP IMPACTS ON INSECT HERBIVORES
inferredcites →https://doi.org/10.1890/04-1257openalex-snapshot
LATITUDINAL VARIATION IN PALATABILITY OF SALT-MARSH PLANTS: ARE DIFFERENCES CONSTITUTIVE?
inferredcites →https://doi.org/10.1890/08-0222.1openalex-snapshot
Latitudinal variation in herbivore pressure in Atlantic Coast salt marshes
inferredcites →https://doi.org/10.2307/1931800openalex-snapshot
Energy Flow of a Salt Marsh Grasshopper Population
inferredcites →https://doi.org/10.2307/1935374openalex-snapshot
Geographic Size Variation in Birds and Its Relationship to Climate
inferredcites →https://doi.org/10.2307/1936032openalex-snapshot
On the Ecological Significance of Bergmann's Rule
inferredcites →https://doi.org/10.2307/1937508openalex-snapshot
An Experimental Test of the Effects of Predation Risk on Habitat Use in Fish
inferredcites →https://doi.org/10.2307/1938021openalex-snapshot
Crowding and Host Plant Nutrition: Environmental Determinants of Wing‐form in Prokelisia marginata
inferredcites →https://doi.org/10.2307/2265730openalex-snapshot
Are Tropical Plants Better Defended? Palatability and Defenses of Temperate vs. Tropical Seaweeds
inferredcites →https://doi.org/10.2307/2963487openalex-snapshot
Habitat Persistence Underlies Intraspecific Variation in the Dispersal Strategies of Planthoppers
inferredcites →https://doi.org/10.2331/suisan.27.395openalex-snapshot
BIOLOGY OF THE SEA-HARE, APLYSIA JULIANA, AS A PREDATOR OF THE BROWN SEAWEED, UNDARIA PINNATIFIDA-I
inferredcites →https://doi.org/10.5962/bhl.part.11725openalex-snapshot
Revision of the world species of Aplysia (Gastropoda, Opisthobrancia)
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1007/s13127-020-00471-yzenodo-depositor-declared
From biggest to smallest mud dragons: size-latitude trends in a group of meiobenthic animals worldwide
inferred← citeshttps://doi.org/10.1002/ajpa.22002openalex-snapshot
Testing Bergmann's rule and the resource seasonality hypothesis in Malagasy primates using GIS‐based climate data
inferred← citeshttps://doi.org/10.1002/ece3.1openalex-snapshot
Natural selection on body size is mediated by multiple interacting factors: a comparison of beetle populations varying naturally and experimentally in body size
inferred← citeshttps://doi.org/10.1002/ece3.5883openalex-snapshot
The fiddler crab, Minuca pugnax, follows Bergmann's rule
inferred← citeshttps://doi.org/10.1002/ece3.8913openalex-snapshot
Oh, the places you will grow: Intraspecific latitudinal clines in butterfly size suggest a phylogenetic signal
inferred← citeshttps://doi.org/10.1002/jez.b.22602openalex-snapshot
Do turtles follow the rules? Latitudinal gradients in species richness, body size, and geographic range area of the world's turtles
inferred← citeshttps://doi.org/10.1002/oik.11426openalex-snapshot
Functional and phylogenetic beta diversity response of nocturnal moth assemblages to land‐use intensity in grasslands and forests
inferred← citeshttps://doi.org/10.1007/s00227-010-1486-5openalex-snapshot
Variation in size of living articulated brachiopods with latitude and depth
inferred← citeshttps://doi.org/10.1007/s00442-013-2785-6openalex-snapshot
Life history traits associated with body size covary along a latitudinal gradient in a generalist grasshopper
inferred← citeshttps://doi.org/10.1007/s00442-016-3603-8openalex-snapshot
Larval growth rate is associated with the composition of the gut microbiota in the Glanville fritillary butterfly
inferred← citeshttps://doi.org/10.1007/s10336-016-1383-xopenalex-snapshot
Morphological variation in the specialist Dupont’s Lark Chersophilus duponti: geographical clines vs. local ecological determinants
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/s11692-024-09628-5openalex-snapshot
Bergmann-Rensch Continuum Under Shell: Gender-Specific Trend in Response to Latitudinal Gradient
inferred← citeshttps://doi.org/10.1016/j.baae.2018.09.002openalex-snapshot
Shallow water ray-finned marine fishes follow Bergmann’s rule
inferred← citeshttps://doi.org/10.1016/j.jcz.2011.12.003openalex-snapshot
Observations on variation in skull size of three mammals in Israel during the 20th century
inferred← citeshttps://doi.org/10.1017/9781108683319.002openalex-snapshot
Extreme environments: responses and adaptation to change
inferred← citeshttps://doi.org/10.1017/9781108683319.003openalex-snapshot
Physiological traits of the Greenland sharkSomniosus microcephalusobtained during the TUNU-Expeditions to Northeast Greenland
inferred← citeshttps://doi.org/10.1017/9781108683319.004openalex-snapshot
Metazoan adaptation to deep-sea hydrothermal vents
inferred← citeshttps://doi.org/10.1017/9781108683319.005openalex-snapshot
Extremophiles populating high-level natural radiation areas (HLNRAs) in Iran
inferred← citeshttps://doi.org/10.1017/9781108683319.006openalex-snapshot
Biodiversity, bioenergetic processes, and biotic and abiotic interactions
inferred← citeshttps://doi.org/10.1017/9781108683319.007openalex-snapshot
Metazoan life in anoxic marine sediments
inferred← citeshttps://doi.org/10.1017/9781108683319.009openalex-snapshot
Vertebrate viruses in polar ecosystems
inferred← citeshttps://doi.org/10.1017/9781108683319.010openalex-snapshot
Life in extreme environments and the responses to change: the example of polar environments
inferred← citeshttps://doi.org/10.1017/9781108683319.011openalex-snapshot
Life in the extreme environments of our planet under pressure
inferred← citeshttps://doi.org/10.1017/9781108683319.012openalex-snapshot
The ecophysiology of responding to change in polar marine benthos
inferred← citeshttps://doi.org/10.1017/9781108683319.013openalex-snapshot
The Southern Ocean: an extreme environment or just home of unique ecosystems?
inferred← citeshttps://doi.org/10.1017/9781108683319.014openalex-snapshot
Microorganisms in cryoturbated organic matter of Arctic permafrost soils
inferred← citeshttps://doi.org/10.1017/9781108683319.015openalex-snapshot
Chemical ecology in the Southern Ocean
inferred← citeshttps://doi.org/10.1017/9781108683319.016openalex-snapshot
Metabolic and taxonomic diversity in antarctic subglacial environments
inferred← citeshttps://doi.org/10.1017/9781108683319.018openalex-snapshot
Analytical astrobiology: the search for life signatures and the remote detection of biomarkers through their Raman spectral interrogation
inferred← citeshttps://doi.org/10.1017/9781108683319.019openalex-snapshot
Adaptation/acclimatisation mechanisms of oxyphototrophic microorganisms and their relevance to astrobiology
inferred← citeshttps://doi.org/10.1017/s0025315416001557openalex-snapshot
Connecting pH with body size in the marine gastropod Trophon geversianus in a latitudinal gradient along the south-western Atlantic coast
inferred← citeshttps://doi.org/10.1038/s41437-019-0239-6openalex-snapshot
Genomic and phenotypic consequences of two independent secondary contact zones between allopatric lineages of the anadromous ice goby Leucopsarion petersii
inferred← citeshttps://doi.org/10.1038/s41467-022-32108-3openalex-snapshot
Thermal adaptation best explains Bergmann’s and Allen’s Rules across ecologically diverse shorebirds
inferred← citeshttps://doi.org/10.1086/671170openalex-snapshot
The Relative Importance of Predation Risk and Water Temperature in Maintaining Bergmann’s Rule in a Marine Ectotherm
inferred← citeshttps://doi.org/10.1086/682072openalex-snapshot
Macronutrient Balance Modulates the Temperature-Size Rule in an Ectotherm
inferred← citeshttps://doi.org/10.1086/695767openalex-snapshot
Southern Ocean Mesopelagic Fish Comply with Bergmann’s Rule
inferred← citeshttps://doi.org/10.1093/biolinnean/bly209openalex-snapshot
Pacific island invasions: how do settlement time, latitude, island area and number of competitors affect body size of the kiore (Polynesian rat) across the Pacific?
inferred← citeshttps://doi.org/10.1093/jisesa/iey121openalex-snapshot
Morphological Variation Tracks Environmental Gradients in an Agricultural Pest,Phaulacridium vittatum(Orthoptera: Acrididae)
inferred← citeshttps://doi.org/10.1093/zoolinnean/zlz080openalex-snapshot
Latitudinal gradients in body size in marine tardigrades
inferred← citeshttps://doi.org/10.1098/rsbl.2017.0453openalex-snapshot
Tropical bird species have less variable body sizes
inferred← citeshttps://doi.org/10.1101/2024.10.30.621136openalex-snapshot
Spiders bring new insight into the eco-evolutionary drivers of body size variation and sexual size dimorphism in arthropods
inferred← citeshttps://doi.org/10.1101/775957openalex-snapshot
Mechanistic macroecology: exploring the drivers of latitudinal variation in terrestrial body size in a General Ecosystem Model
inferred← citeshttps://doi.org/10.1111/1365-2435.70281openalex-snapshot
Bergmann's rule: Why does body size increase with latitude?
inferred← citeshttps://doi.org/10.1111/1365-2656.70359openalex-snapshot
Beta diversity of Arctiinae moths (Lepidoptera: Erebidae) along a recovering tropical forest gradient
inferred← citeshttps://doi.org/10.1111/1365-2745.12137openalex-snapshot
Importance of local vs. geographic variation in salt marsh plant quality for arthropod herbivore communities
inferred← citeshttps://doi.org/10.1111/1744-7917.12027openalex-snapshot
Humidity and seasonality drives body size patterns in males of the bush cricket Isophya rizeensis Sevgili, 2003 (Orthoptera: Tettigoniidae: Phaneropterinae)
inferred← citeshttps://doi.org/10.1111/bij.12900openalex-snapshot
Evolution of gigantism and size-based female mate choice in ice goby (Leucopsarion petersii) populations in a semi-enclosed sea basin
inferred← citeshttps://doi.org/10.1111/brv.13081openalex-snapshot
Diet effects on ectotherm thermal performance
inferred← citeshttps://doi.org/10.1111/ecog.03917openalex-snapshot
Moth body size increases with elevation along a complete tropical elevational gradient for two hyperdiverse clades
inferred← citeshttps://doi.org/10.1111/ecog.05545openalex-snapshot
Testing Bergmann's rule in marine copepods
inferred← citeshttps://doi.org/10.1111/ecog.06452openalex-snapshot
Do marine planktonic ciliates follow Bergmann's rule?
inferred← citeshttps://doi.org/10.1111/een.12151openalex-snapshot
Genetic, morphological, and dietary changes associated with novel habitat colonisation in the C anary I sland endemic grasshopper A crostira bellamyi
inferred← citeshttps://doi.org/10.1111/ele.14375openalex-snapshot
Mean reef fish body size decreases towards warmer waters
inferred← citeshttps://doi.org/10.1111/eva.12129openalex-snapshot
Climate warming and Bergmann's rule through time: is there any evidence?
inferred← citeshttps://doi.org/10.1111/gcb.16860openalex-snapshot
A global assessment of Bergmann's rule in mammals and birds
inferred← citeshttps://doi.org/10.1111/j.1095-8312.2012.02028.xopenalex-snapshot
Temporal and geographical variation in skull size of the red fox (Vulpes vulpes) and the Eurasian badger (Meles meles) in Austria
inferred← citeshttps://doi.org/10.1111/j.1365-2699.2012.02710.xopenalex-snapshot
Patterns in body size and melanism along a latitudinal cline in the wingless grasshopper,Phaulacridium vittatum
inferred← citeshttps://doi.org/10.1111/j.1420-9101.2010.02174.xopenalex-snapshot
Limited gene flow may enhance adaptation to local optima in isolated populations of the Roesel’s bush cricket (Metrioptera roeselii)
inferred← citeshttps://doi.org/10.1111/j.1469-185x.2010.00168.xopenalex-snapshot
Recent spatial and temporal changes in body size of terrestrial vertebrates: probable causes and pitfalls
inferred← citeshttps://doi.org/10.1111/j.1600-0706.2010.18670.xopenalex-snapshot
Are latitudinal clines in body size adaptive?
inferred← citeshttps://doi.org/10.1111/j.1600-0706.2011.19593.xopenalex-snapshot
The role of host seed size in mediating a latitudinal body size cline in an introduced bruchid beetle in Japan
inferred← citeshttps://doi.org/10.1111/jbi.14730openalex-snapshot
Water temperature and season length interact to explain a rare non‐linear ecogeographic cline in body size
inferred← citeshttps://doi.org/10.1111/jbi.70158openalex-snapshot
Eco‐Evolutionary Drivers of Body Size Variation in Arthropods, With a Focus on Spiders
inferred← citeshttps://doi.org/10.1111/let.12104openalex-snapshot
Normal giants? Temporal and latitudinal shifts of Palaeozoic marine invertebrate gigantism and global change
inferred← citeshttps://doi.org/10.1111/let.12324openalex-snapshot
Conch size evolution of Silurian–Devonian tentaculitoids
inferred← citeshttps://doi.org/10.1111/mam.12229openalex-snapshot
Latitudinal and seasonal plasticity in American bison Bison bison diets
inferred← citeshttps://doi.org/10.1111/oik.03468openalex-snapshot
How foraging allometries and resource dynamics could explain Bergmann's rule and the body‐size diet relationship in mammals
inferred← citeshttps://doi.org/10.1111/oik.03698openalex-snapshot
Bergmann's rule: a biophysiological rule examined in birds
inferred← citeshttps://doi.org/10.1134/s2079086414030098openalex-snapshot
On the applicability of Bergmann’s rule to ectotherms: The state of the art
inferred← citeshttps://doi.org/10.1242/jeb.067066openalex-snapshot
Why might they be giants? Towards an understanding of polar gigantism
inferred← citeshttps://doi.org/10.1242/jeb.242846openalex-snapshot
Diet mediates thermal performance traits: implications for marine ectotherms
inferred← citeshttps://doi.org/10.1371/journal.pone.0015323openalex-snapshot
Global Patterns and Predictions of Seafloor Biomass Using Random Forests
inferred← citeshttps://doi.org/10.1371/journal.pone.0059829openalex-snapshot
Preference and Performance in Plant–Herbivore Interactions across Latitude–A Study in U.S. Atlantic Salt Marshes
inferred← citeshttps://doi.org/10.1371/journal.pone.0288276openalex-snapshot
Effects of leaf traits of tropical trees on the abundance and body mass of herbivorous arthropod communities
inferred← citeshttps://doi.org/10.1525/cond.2013.120031openalex-snapshot
Minimal Genetic Structure in the Cerulean Warbler Despite Evidence for Ecological Differentiation among Populations
inferred← citeshttps://doi.org/10.1890/10-1523.1openalex-snapshot
Regulation of animal size by eNPP, Bergmann's rule, and related phenomena
inferred← citeshttps://doi.org/10.26215/heal.uoa.8600openalex-snapshot
Variation in body size of terrestrial isopods (crustacea: oniscidea) and application of ecogeographical rules
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