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Geographic variation and thermal plasticity shape salamander metabolic rates under current and future climates
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/2017jd027283openalex-snapshot
Maximum and Minimum Soil Surface Temperature Trends Over China, 1965–2014
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Evaluating within‐population variability in behavior and demography for the adaptive potential of a dispersal‐limited species to climate change
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Low acclimation capacity of narrow‐ranging thermal specialists exposes susceptibility to global climate change
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The Bogert effect revisited: Salamander regulatory behaviors are differently constrained by time and space
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Geographic variation and thermal plasticity shape salamander metabolic rates under current and future climates
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Local adaptation reduces the metabolic cost of environmental warming
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Evaluating changes in season length, onset, and end dates across the United States (1948–2012)
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WorldClim 2: new 1‐km spatial resolution climate surfaces for global land areas
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Physiological flexibility in the Andean lizard Liolaemus bellii: seasonal changes in energy acquisition, storage and expenditure
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Past and future changes in climate and hydrological indicators in the US Northeast
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Spatial variation in water loss predicts terrestrial salamander distribution and population dynamics
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Regional climate change projections for the Northeast USA
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Acclimation to constant and variable temperatures in plethodontid salamanders—I. Rates of oxygen consumption
inferredcites →https://doi.org/10.1016/j.agrformet.2003.08.030openalex-snapshot
Soil temperature under forests: a simple model for predicting soil temperature under a range of forest types
inferredcites →https://doi.org/10.1016/j.jtherbio.2010.01.006openalex-snapshot
Influence of temperature and body mass on standard metabolic rate of eastern red-backed salamanders (Plethodon cinereus)
inferredcites →https://doi.org/10.1016/j.jtherbio.2016.06.010openalex-snapshot
Thermal equilibrium and temperature differences among body regions in European plethodontid salamanders
inferredcites →https://doi.org/10.1038/nature09407openalex-snapshot
Global metabolic impacts of recent climate warming
inferredcites →https://doi.org/10.1038/nclimate2457openalex-snapshot
Physiological plasticity increases resilience of ectothermic animals to climate change
inferredcites →https://doi.org/10.1038/ncomms15399openalex-snapshot
A dynamic eco-evolutionary model predicts slow response of alpine plants to climate warming
inferredcites →https://doi.org/10.1038/s41467-018-03384-9openalex-snapshot
Strong phenotypic plasticity limits potential for evolutionary responses to climate change
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The ecological importance of intraspecific variation
inferredcites →https://doi.org/10.1046/j.1523-1739.2001.015003558.xopenalex-snapshot
A Case for Using Plethodontid Salamanders for Monitoring Biodiversity and Ecosystem Integrity of North American Forests
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Energetic consequences of metabolic depression in tropical and temperate-zone lizards
inferredcites →https://doi.org/10.1073/pnas.0709472105openalex-snapshot
Impacts of climate warming on terrestrial ectotherms across latitude
inferredcites →https://doi.org/10.1073/pnas.1702584114openalex-snapshot
Behavioral responses to annual temperature variation alter the dominant energy pathway, growth, and condition of a cold-water predator
inferredcites →https://doi.org/10.1073/pnas.212251999openalex-snapshot
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inferredcites →https://doi.org/10.1086/381872openalex-snapshot
Effects of Body Size and Temperature on Population Growth
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Linking Traits to Energetics and Population Dynamics to Predict Lizard Ranges in Changing Environments
inferredcites →https://doi.org/10.1093/acprof:oso/9780195310610.001.0001openalex-snapshot
Measuring Metabolic Rates
inferredcites →https://doi.org/10.1093/acprof:oso/9780198570875.001.1openalex-snapshot
Thermal Adaptation
inferredcites →https://doi.org/10.1093/acprof:oso/9780198570875.003.0005openalex-snapshot
Thermal Acclimation
inferredcites →https://doi.org/10.1093/icb/19.1.357openalex-snapshot
Integrating Thermal Physiology and Ecology of Ectotherms: A Discussion of Approaches
inferredcites →https://doi.org/10.1093/icb/icj003openalex-snapshot
Are mountain passes higher in the tropics? janzen's hypothesis revisited
inferredcites →https://doi.org/10.1098/rspb.2011.1778openalex-snapshot
What causes intraspecific variation in resting metabolic rate and what are its ecological consequences?
inferredcites →https://doi.org/10.1098/rspb.2013.1869openalex-snapshot
A heuristic model on the role of plasticity in adaptive evolution: plasticity increases adaptation, population viability and genetic variation
inferredcites →https://doi.org/10.1098/rspb.2015.0401openalex-snapshot
Plasticity in thermal tolerance has limited potential to buffer ectotherms from global warming
inferredcites →https://doi.org/10.1098/rspb.2015.1946openalex-snapshot
Why does offspring size affect performance? Integrating metabolic scaling with life-history theory
inferredcites →https://doi.org/10.1098/rspb.2016.0323openalex-snapshot
Metabolic rate covaries with fitness and the pace of the life history in the field
inferredcites →https://doi.org/10.1098/rspb.2017.0386openalex-snapshot
Evolution of plasticity and adaptive responses to climate change along climate gradients
inferredcites →https://doi.org/10.1098/rstb.2012.0005openalex-snapshot
Predicting organismal vulnerability to climate warming: roles of behaviour, physiology and adaptation
inferredcites →https://doi.org/10.1098/rstb.2018.0180openalex-snapshot
Ecological and evolutionary consequences of metabolic rate plasticity in response to environmental change
inferredcites →https://doi.org/10.1111/1365-2435.12098openalex-snapshot
Climate warming and ectotherm body size – from individual physiology to community ecology
inferredcites →https://doi.org/10.1111/1365-2435.12406openalex-snapshot
Thermoregulatory behaviour limits local adaptation of thermal niches and confers sensitivity to climate change
inferredcites →https://doi.org/10.1111/1365-2656.12083openalex-snapshot
Phenotypic clines, energy balances and ecological responses to climate change
inferredcites →https://doi.org/10.1111/ele.12348openalex-snapshot
The effects of phenotypic plasticity and local adaptation on forecasts of species range shifts under climate change
inferredcites →https://doi.org/10.1111/ele.12686openalex-snapshot
Can we predict ectotherm responses to climate change using thermal performance curves and body temperatures?
inferredcites →https://doi.org/10.1111/ele.13107openalex-snapshot
The complex drivers of thermal acclimation and breadth in ectotherms
inferredcites →https://doi.org/10.1111/ele.13636openalex-snapshot
Three questions about the eco‐physiology of overwintering underground
inferredcites →https://doi.org/10.1111/eva.12108openalex-snapshot
Evolutionary and plastic responses of freshwater invertebrates to climate change: realized patterns and future potential
inferredcites →https://doi.org/10.1111/eva.12114openalex-snapshot
Plasticity and genetic adaptation mediate amphibian and reptile responses to climate change
inferredcites →https://doi.org/10.1111/gcb.13000openalex-snapshot
Intraspecific trait variation across scales: implications for understanding global change responses
inferredcites →https://doi.org/10.1111/gcb.13211openalex-snapshot
Population variability complicates the accurate detection of climate change responses
inferredcites →https://doi.org/10.1111/gcb.14562openalex-snapshot
Incorporating local adaptation into forecasts of species’ distribution and abundance under climate change
inferredcites →https://doi.org/10.1111/j.1365-2435.2010.01813.xopenalex-snapshot
Thermal plasticity of metabolic rates linked to life-history traits and foraging behaviour in a parasitic wasp
inferredcites →https://doi.org/10.1111/j.1461-0248.2008.01277.xopenalex-snapshot
Mechanistic niche modelling: combining physiological and spatial data to predict species’ ranges
inferredcites →https://doi.org/10.1111/j.1472-4642.2010.00641.xopenalex-snapshot
Moving beyond static species distribution models in support of conservation biogeography
inferredcites →https://doi.org/10.1111/j.1558-5646.1949.tb00021.xopenalex-snapshot
THERMOREGULATION IN REPTILES, A FACTOR IN EVOLUTION
inferredcites →https://doi.org/10.1111/j.1558-5646.2008.00603.xopenalex-snapshot
NATURAL SELECTION REDUCES ENERGY METABOLISM IN THE GARDEN SNAIL,HELIX ASPERSA(CORNU ASPERSUM)
inferredcites →https://doi.org/10.1111/j.1570-7458.2010.01067.xopenalex-snapshot
Thermal variability alters climatic stress resistance and plastic responses in a globally invasive pest, the Mediterranean fruit fly ( Ceratitis capitata )
inferredcites →https://doi.org/10.1126/sciadv.aar5471openalex-snapshot
Plasticity reveals hidden resistance to extinction under climate change in the global hotspot of salamander diversity
inferredcites →https://doi.org/10.1126/science.1184695openalex-snapshot
Erosion of Lizard Diversity by Climate Change and Altered Thermal Niches
inferredcites →https://doi.org/10.1126/science.aaa4984openalex-snapshot
Accelerating extinction risk from climate change
inferredcites →https://doi.org/10.1126/science.aad8466openalex-snapshot
Improving the forecast for biodiversity under climate change
inferredcites →https://doi.org/10.1139/z02-049openalex-snapshot
Do amphibians follow Bergmann's rule?
inferredcites →https://doi.org/10.1175/1520-0450(2003)042<1139:adstda>2.0.co;2openalex-snapshot
A Daily Soil Temperature Dataset and Soil Temperature Climatology of the Contiguous United States
inferredcites →https://doi.org/10.1175/bams-d-11-00197.1openalex-snapshot
NOAA's 1981–2010 U.S. Climate Normals: An Overview
inferredcites →https://doi.org/10.1242/jeb.161984openalex-snapshot
Developmental phenotypic plasticity helps bridge stochastic weather events associated with climate change
inferredcites →https://doi.org/10.1242/jeb.178236openalex-snapshot
Physiological responses to elevated temperature across the geographic range of a terrestrial salamander
inferredcites →https://doi.org/10.1242/jeb.187559openalex-snapshot
Environmental temperature alters the digestive performance and gut microbiota of a terrestrial amphibian
inferredcites →https://doi.org/10.1371/journal.pbio.1002281openalex-snapshot
Live Fast, Die Young: Experimental Evidence of Population Extinction Risk due to Climate Change
inferredcites →https://doi.org/10.1371/journal.pcbi.1006100openalex-snapshot
The AmP project: Comparing species on the basis of dynamic energy budget parameters
inferredcites →https://doi.org/10.1371/journal.pone.0062184openalex-snapshot
Fine-Scale Habitat Associations of a Terrestrial Salamander: The Role of Environmental Gradients and Implications for Population Dynamics
inferredcites →https://doi.org/10.1371/journal.pone.0086854openalex-snapshot
Effects of Red-Backed Salamanders on Ecosystem Functions
inferredcites →https://doi.org/10.1643/ot-14-188openalex-snapshot
Effects of Elevation on Plethodontid Salamander Body Size
inferredcites →https://doi.org/10.1643/ot-14-223openalex-snapshot
Physiology of Plethodontid Salamanders: A Call for Increased Efforts
inferredcites →https://doi.org/10.1670/104-05n.1openalex-snapshot
Effects of Temperature, Sex, and Gravidity on the Metabolism of Small-Mouthed Salamanders, Ambystoma texanum, during the Reproductive Season
inferredcites →https://doi.org/10.18637/jss.v067.i01openalex-snapshot
Fitting Linear Mixed-Effects Models Using lme4
inferredcites →https://doi.org/10.1890/11-0150.1openalex-snapshot
Height‐growth response to climatic changes differs among populations of Douglas‐fir: a novel analysis of historic data
inferredcites →https://doi.org/10.1890/es14-00360.1openalex-snapshot
Geographic variation of resistance to water loss within two species of lungless salamanders: implications for activity
inferredcites →https://doi.org/10.2307/1443655openalex-snapshot
Salamander Populations and Biomass in the Hubbard Brook Experimental Forest, New Hampshire
inferredcites →https://doi.org/10.2307/1444003openalex-snapshot
Microhabitats of a Terrestrial Forest Salamander
inferredcites →https://doi.org/10.2307/1933498openalex-snapshot
The Distribution of the Red‐Backed Salamander, Plethodon C. Cinereus, within the Soil
inferredcites →https://doi.org/10.2307/2389880openalex-snapshot
Seasonal Acclimatization and Latitudinal Compensation in Metabolism: Do They Exist?
inferredcites →https://doi.org/10.32614/r.manualsopenalex-snapshot
R: A Language and Environment for Statistical Computing
inferredcites →https://doi.org/10.3354/cr00897openalex-snapshot
Adaptive phenotypic plasticity and resilience of vertebrates to increasing climatic unpredictability
inferredcites →https://doi.org/10.4236/acs.2015.53014openalex-snapshot
Correlation between Atmospheric Temperature and Soil Temperature: A Case Study for Dhaka, Bangladesh
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4809405openalex-extracted
The Jumping Performance of Two Eleutherodactylus Frogs: The Effect of Temperature
inferred← citeshttps://doi.org/10.1016/j.jtherbio.2025.104113openalex-snapshot
The jumping performance of two Eleutherodactylus frog species: the effect of temperature
inferred← citeshttps://doi.org/10.1016/j.jtherbio.2025.104356openalex-snapshot
Sex and reproductive condition shape thermal acclimation strategy in a plethodontid salamander
inferred← citeshttps://doi.org/10.1093/icb/icag142openalex-snapshot
Weak Coupling Between Gas Exchange and Water Loss in Lungless Salamanders
inferred← citeshttps://doi.org/10.1098/rsbl.2024.0033openalex-snapshot
Range-wide salamander densities reveal a key component of terrestrial vertebrate biomass in eastern North American forests
inferred← citeshttps://doi.org/10.1098/rspb.2025.0374openalex-snapshot
Evolutionary diversity of muscle OXPHOS efficiency in vitro across ectothermic vertebrates
inferred← citeshttps://doi.org/10.1098/rspb.2025.1319openalex-snapshot
Shifts in salamander body size associated with 60 years of climate change
inferred← citeshttps://doi.org/10.1111/eth.13552openalex-snapshot
Thermal Plasticity Changes Competitive Ability Across a Woodland Salamander Hybrid System
inferred← citeshttps://doi.org/10.1111/jbi.14813openalex-snapshot
Climate‐related variation of metabolic rate across the distribution of a broadly tolerant invasive forest pest
inferred← citeshttps://doi.org/10.70675/3c9ce44dz9168z4fb8z9dbdz465c34eb809eopenalex-snapshot
Se reproduire dans des climats changeants : déterminants et conséquences des modifications de la phénologie de la reproduction chez un reptile vivipare
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