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The Allometry of Avian Basal Metabolic Rate: Good Predictions Need Good Data
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Outgoing claims: the papers this work cites, builds on, or argues with.
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Effect of air temperature on the rate of energy metabolism in the English sparrow
inferredcites →https://doi.org/10.1006/jare.2000.0742openalex-snapshot
Heat production and body temperature of Arabian babblers (Turdoides squamiceps): a bird from hot desert habitats
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Energetic Features of Avian Thermoregulatory Responses
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Climatic adaptation in Svian standard metabolic rate
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Ventilation and oxygen consumption inAmazona viridigenalis
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Cost of flight in the zebra finch ( Taenopygia guttata ): a novel approach based on elimination of 13 C labelled bicarbonate
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The influence of climate on the basal metabolic rate of small mammals: a slow-fast metabolic continuum
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Heterothermic responses in the speckled mousebird ( Colius striatus )
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Thermoregulation in the titmouse (Parus major L.)
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The influence of distribution and ecology on the thermoregulation of small birds
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Thermoregulatory responses of the peruvian penguin, Spheniscus humboldti
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Resting metabolic rates of ratite birds: The kiwis and the emu
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Evaporative water loss from birds: Effects of artificial radiation
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inferredcites →https://doi.org/10.1016/0300-9629(81)90157-2openalex-snapshot
Body temperature and metabolism in the red-backed mousebird (Colius castanotus) during fasting and torpor
inferredcites →https://doi.org/10.1016/0300-9629(81)90172-9openalex-snapshot
Bioenergetics of captive Belding's savannah sparrows (Passerculus sanwichensis beldingi)
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inferredcites →https://doi.org/10.1016/0300-9629(82)90061-5openalex-snapshot
Metabolic rate and evaporative water loss in the least seed-snipe, Thinocorus rumicivorus
inferredcites →https://doi.org/10.1016/0300-9629(82)90275-4openalex-snapshot
Torpor and metabolism in hummingbirds
inferredcites →https://doi.org/10.1016/0300-9629(83)90086-5openalex-snapshot
Development of homeothermy in the diving petrels Pelecanoides urinatrix exsul and P. georgicus, and the Antarctic prion Pachyptila desolata
inferredcites →https://doi.org/10.1016/0300-9629(83)90332-8openalex-snapshot
Comparative physiology of the Scrub Jay (Aphelocoma coerulescens) and the Steller's Jay (Cyanocitta Stelleri)
inferredcites →https://doi.org/10.1016/0300-9629(83)90363-8openalex-snapshot
Rates of oxygen consumption in four species of seabird at Palmer Station, Antarctic Peninsula
inferredcites →https://doi.org/10.1016/0300-9629(83)90715-6openalex-snapshot
Metabolic cost of incubation in the Laysan albatross and Bonin petrel
inferredcites →https://doi.org/10.1016/0300-9629(83)90726-0openalex-snapshot
Heat balance of the partridge Alectoris chukar exposed to moderate, high and extreme thermal stress
inferredcites →https://doi.org/10.1016/0300-9629(84)90030-6openalex-snapshot
Metabolic rates of sub-antarctic procellariiformes: A comparative study
inferredcites →https://doi.org/10.1016/0300-9629(84)90071-9openalex-snapshot
Resting metabolic rate and energetic cost of incubation in macaroni penguins Eudyptes chrysolophus and rockhopper penguins E. chrysocome
inferredcites →https://doi.org/10.1016/0300-9629(88)91142-5openalex-snapshot
Seasonal changes in standard metabolic rates in the white-browed scrubwren Sericornis frontalis (Acanthizidae) from arid, semi-arid and mesic environments
inferredcites →https://doi.org/10.1016/0300-9629(89)90154-0openalex-snapshot
Metabolism in malleefowl (Leipoa ocellata)
inferredcites →https://doi.org/10.1016/0300-9629(89)90581-1openalex-snapshot
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inferredcites →https://doi.org/10.1016/0300-9629(92)90190-2openalex-snapshot
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inferredcites →https://doi.org/10.1016/s1095-6433(01)00499-8openalex-snapshot
Metabolism, body temperature and thermal conductance of fruit-doves (Aves: Columbidae, Treroninae)
inferredcites →https://doi.org/10.1038/417166aopenalex-snapshot
Allometric cascade as a unifying principle of body mass effects on metabolism
inferredcites →https://doi.org/10.1038/44766openalex-snapshot
Inferring the historical patterns of biological evolution
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Is ‘nocturnal hypothermia’ a valid physiological concept in small birds?: a study on Bronze MannikinsSpermestes cucullatus
inferredcites →https://doi.org/10.1071/zo9770193openalex-snapshot
Temperature regulation in the Dusky Munia, Lonchura fuscans (Cassin) (Estrildidae)
inferredcites →https://doi.org/10.1071/zo98058openalex-snapshot
Thermoregulation and ventilation in the tawny frogmouth, Podargus strigoides : a low-metabolic avian species
inferredcites →https://doi.org/10.1071/zo9860025openalex-snapshot
Thermoregulation, Oxygen-Consumption and Water Turnover in Stubble Quail, Coturnix-Pectoralis, and King Quail, Coturnix-Chinensis
inferredcites →https://doi.org/10.1071/zo99023openalex-snapshot
Standard metabolic rates of three nectarivorous meliphagid passerine birds
inferredcites →https://doi.org/10.1071/zo9910131openalex-snapshot
Metabolism and Water Flux of Captive and Free-Living Australian Parrots
inferredcites →https://doi.org/10.1071/zo9960445openalex-snapshot
Field Metabolic Rate and Water Flux of Nectarivorous Honeyeaters
inferredcites →https://doi.org/10.1073/pnas.012579799openalex-snapshot
Allometric scaling of metabolic rate from molecules and mitochondria to cells and mammals
inferredcites →https://doi.org/10.1073/pnas.162216899openalex-snapshot
Supply–demand balance and metabolic scaling
inferredcites →https://doi.org/10.1080/00040851.1972.12003640openalex-snapshot
Bioenergetics of the Snowy Owl ( Nyctea Scandiaca )
inferredcites →https://doi.org/10.1086/284325openalex-snapshot
Phylogenies and the Comparative Method
inferredcites →https://doi.org/10.1086/285877openalex-snapshot
Phylogenetic Analysis of Avian Energetics: Passerines and Nonpasserines Do Not Differ
inferredcites →https://doi.org/10.1086/303327openalex-snapshot
Using the Past to Predict the Present: Confidence Intervals for Regression Equations in Phylogenetic Comparative Methods
inferredcites →https://doi.org/10.1086/303383openalex-snapshot
The Zoogeography of Mammalian Basal Metabolic Rate
inferredcites →https://doi.org/10.1086/317740openalex-snapshot
The Adjustment of Avian Metabolic Rates and Water Fluxes to Desert Environments
inferredcites →https://doi.org/10.1086/319669openalex-snapshot
Thermoregulation and the Energetic Significance of Clustering Behavior in the White‐Backed Mousebird (Colius colius)
inferredcites →https://doi.org/10.1086/341998openalex-snapshot
Physiological Adjustments to Arid and Mesic Environments in Larks (Alaudidae)
inferredcites →https://doi.org/10.1086/342803openalex-snapshot
Metabolic and Thermal Physiology of Pigeons and Doves
inferredcites →https://doi.org/10.1086/343873openalex-snapshot
Phylogenetic Analysis and Comparative Data: A Test and Review of Evidence
inferredcites →https://doi.org/10.1086/515881openalex-snapshot
On the Utility of Uniformity in the Definition of Basal Rate of Metabolism
inferredcites →https://doi.org/10.1086/physzool.28.3.30159915openalex-snapshot
The Metabolism of Some Alaskan Animals in Winter and Summer
inferredcites →https://doi.org/10.1086/physzool.33.4.30152668openalex-snapshot
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inferredcites →https://doi.org/10.1086/physzool.37.3.30152402openalex-snapshot
Thermal and Metabolic Responses of the Gray Jay to Cold Stress
inferredcites →https://doi.org/10.1086/physzool.46.1.30152517openalex-snapshot
Temperature Regulation of the Pyrrhuloxia and the Arizona Cardinal
inferredcites →https://doi.org/10.1086/physzool.50.1.30155714openalex-snapshot
Respiration, Metabolism, and Heat Exchange of Euthermic and Torpid Poorwills and Hummingbirds
inferredcites →https://doi.org/10.1086/physzool.53.4.30157874openalex-snapshot
Metabolism and Solar Radiation in Dark and White Herons in Hot Climates
inferredcites →https://doi.org/10.1086/physzool.54.3.30159949openalex-snapshot
Physiological Thermoregulation in Heat-Stressed Birds: Consequences of Body Size
inferredcites →https://doi.org/10.1086/physzool.56.2.30156052openalex-snapshot
Environmental Influences on the Energetics and Behavior of Anhingas and Double-Crested Cormorants
inferredcites →https://doi.org/10.1086/physzool.56.3.30152601openalex-snapshot
Energy Metabolism and Nocturnal Hypothermia in Two Tropical Passerine Frugivores, Manacus vitellinus and Pipra mentalis
inferredcites →https://doi.org/10.1086/physzool.56.4.30155880openalex-snapshot
Energy, Water, and Solute Balance of the Ostrich Struthio camelus
inferredcites →https://doi.org/10.1086/physzool.59.6.30158612openalex-snapshot
Daily Energy expenditure by Adult Leach's Storm-Petrels during the Nesting Cycle
inferredcites →https://doi.org/10.1086/physzool.66.1.30158285openalex-snapshot
Black-Bellied Sandgrouse (Pterocles orientalis) and Pin-Tailed Sandgrouse (Pterocles alchata): Closely Related Species with Differing Bioenergetic Adaptations to Arid Zones
inferredcites →https://doi.org/10.1086/physzool.66.4.30163806openalex-snapshot
Seasonal Patterns of Time and Energy Allocation by Birds
inferredcites →https://doi.org/10.1093/auk/100.4.977openalex-snapshot
Basal Metabolism of the Apapane: Comparison of Freshly Caught Birds with Long-term Captives
inferredcites →https://doi.org/10.1093/auk/101.1.25openalex-snapshot
Reproductive Energetics of Two Tropical Bird Species
inferredcites →https://doi.org/10.1093/auk/94.1.72openalex-snapshot
Oxygen Consumption, Evaporative Water Loss, and Body Temperature in the Sooty Tern
inferredcites →https://doi.org/10.1093/auk/99.4.667openalex-snapshot
Temperature Regulation in Two Endangered Hawaiian Honeycreepers: The Palila (Psittirostra bailleui) and the Laysan Finch (Psittirostra cantans)
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/42.3.265openalex-snapshot
Phylogenetic Analysis of Covariance by Computer Simulation
inferredcites →https://doi.org/10.1111/j.1469-7998.1987.tb03708.xopenalex-snapshot
Active and resting metabolism in birds: allometry, phylogeny and ecology
inferredcites →https://doi.org/10.1111/j.1469-7998.1998.tb00004.xopenalex-snapshot
Circadian metabolic and thermoregulatory patterns of red‐billed woodhoopoes (Phoeniculus purpureus): the influence of huddling
inferredcites →https://doi.org/10.1111/j.1748-1716.1957.tb01485.xopenalex-snapshot
Heat Regulation and Metabolism in some Tropical Mammals and Birds.
inferredcites →https://doi.org/10.1126/science.284.5420.1677openalex-snapshot
The Fourth Dimension of Life: Fractal Geometry and Allometric Scaling of Organisms
inferredcites →https://doi.org/10.1126/science.635577openalex-snapshot
Behavioral Thermoregulation: Orientation Toward the Sun in Herring Gulls
inferredcites →https://doi.org/10.1126/science.835018openalex-snapshot
Terrestrial Locomotion in Penguins: It Costs More to Waddle
inferredcites →https://doi.org/10.1139/z75-007openalex-snapshot
The energy cycle and thermal tolerance of the starlings (Aves, Sturnidae) in North America
inferredcites →https://doi.org/10.1139/z92-003openalex-snapshot
Winter energy requirements of blue grouse
inferredcites →https://doi.org/10.1152/ajplegacy.1932.101.2.260openalex-snapshot
THE BASAL METABOLISM OF THE MOURNING DOVE AND SOME OF ITS HYBRIDS
inferredcites →https://doi.org/10.1152/ajplegacy.1967.213.4.883openalex-snapshot
Temperature regulation and evaporation in the pigeon and the roadrunner
inferredcites →https://doi.org/10.1152/ajplegacy.1976.231.3.903openalex-snapshot
Energy expenditure for thermoregulation and locomotion in emperor penguins
inferredcites →https://doi.org/10.1152/ajpregu.1990.259.2.r333openalex-snapshot
Avian basal metabolic rates: their association with body composition and energy expenditure in nature
inferredcites →https://doi.org/10.1242/jeb.205.1.101openalex-snapshot
Passerinesversusnonpasserines: so far, no statistical differences in the scaling of avian energetics
inferredcites →https://doi.org/10.1242/jeb.205.4.475openalex-snapshot
Heart rate and energy expenditure of incubating wandering albatrosses: basal levels, natural variation, and the effects of human disturbance
inferredcites →https://doi.org/10.12987/9780300237856openalex-snapshot
Phylogeny and Classification of the Birds
inferredcites →https://doi.org/10.1642/0004-8038(2001)118[0781:saceoa]2.0.co;2openalex-snapshot
Standard and Comparative Energetics of a Small Avian Herbivore (Phytotoma rara)
inferredcites →https://doi.org/10.1642/0004-8038(2001)118[0916:eotaba]2.0.co;2openalex-snapshot
ENERGETICS OF TOUCANS, A BARBET, AND A HORNBILL: IMPLICATIONS FOR AVIAN FRUGIVORY
inferredcites →https://doi.org/10.2307/1365200openalex-snapshot
Bioenergetics of Growth in Nestling Wood Storks
inferredcites →https://doi.org/10.2307/1365224openalex-snapshot
Physiological Responses to Temperature in the Common Nighthawk
inferredcites →https://doi.org/10.2307/1365471openalex-snapshot
Food and Oxygen Consumption in Three Species of Owls (Strigidae)
inferredcites →https://doi.org/10.2307/1365995openalex-snapshot
Relation of Metabolism to Ambient Temperature in the Verdin
inferredcites →https://doi.org/10.2307/1366012openalex-snapshot
Temperature Regulation in the Little Papuan Frogmouth, Podargus ocellatus
inferredcites →https://doi.org/10.2307/1366047openalex-snapshot
Responses to Temperature by the Spotted Nightjar (Eurostopodus guttatus)
inferredcites →https://doi.org/10.2307/1366305openalex-snapshot
Respiratory Metabolism of the Red-Winged Blackbird in Relation to Ambient Temperature
inferredcites →https://doi.org/10.2307/1366368openalex-snapshot
A Re-Examination of the Relation between Standard Metabolic Rate and Body Weight in Birds
inferredcites →https://doi.org/10.2307/1366605openalex-snapshot
Migration and Bioenergetics of Flight in the Pacific Golden Plover
inferredcites →https://doi.org/10.2307/1366621openalex-snapshot
Thermoregulation in the Red-Breasted Nuthatch (Sitta canadensis)
inferredcites →https://doi.org/10.2307/1366623openalex-snapshot
Temperature Regulation in the Speckled Mousebird, Colius striatus
inferredcites →https://doi.org/10.2307/1366710openalex-snapshot
Standard Metabolism Comparisons between Orders of Birds
inferredcites →https://doi.org/10.2307/1366730openalex-snapshot
Seasonal Variation in the Metabolism and Thyroid Activity of the Black-Capped Chickadee (Parus atricapillus)
inferredcites →https://doi.org/10.2307/1367037openalex-snapshot
Basal Metabolic Rate and Energy Expenditure during Incubation in the Wandering Albatross (Diomedea exulans)
inferredcites →https://doi.org/10.2307/1367113openalex-snapshot
Effects of Nasal Tufts and Nasal Respiration on Thermoregulation and Evaporative Water Loss in the Common Crow
inferredcites →https://doi.org/10.2307/1367336openalex-snapshot
Temperature Regulation and Climatic Adaptation in Black-Billed and Yellow-Billed Magpies
inferredcites →https://doi.org/10.2307/1367753openalex-snapshot
The Relationship of Energetics of Falconiform Birds to Body Mass and Climate
inferredcites →https://doi.org/10.2307/1367864openalex-snapshot
Metabolic Rate in Five Tropical Bird Species
inferredcites →https://doi.org/10.2307/1368192openalex-snapshot
Daily Allocation of Time and Energy of Western Bluebirds Feeding Nestlings
inferredcites →https://doi.org/10.2307/1368232openalex-snapshot
Breeding Energetics and Thermal Ecology of the Acorn Woodpecker in Central Coastal California
inferredcites →https://doi.org/10.2307/1368498openalex-snapshot
Metabolic, Water and Thermal Relations of the Chilean Tinamou
inferredcites →https://doi.org/10.2307/1368732openalex-snapshot
Metabolic and Respiratory Physiology of an Arid-Adapted Australian Bird, the Spinifex Pigeon
inferredcites →https://doi.org/10.2307/1370011openalex-snapshot
Heat Production and Evaporative Water Loss of Dune Larks from the Namib Desert
inferredcites →https://doi.org/10.2307/1370228openalex-snapshot
Energetics, Thermoregulation and Nocturnal Hypothermia in Australian Silvereyes
inferredcites →https://doi.org/10.2307/1538742openalex-snapshot
ADAPTATION TO COLD IN ARCTIC AND TROPICAL MAMMALS AND BIRDS IN RELATION TO BODY TEMPERATURE, INSULATION, AND BASAL METABOLIC RATE
inferredcites →https://doi.org/10.2307/1550225openalex-snapshot
Bioenergetics of the Snowy Owl (Nyctea scandiaca)
inferredcites →https://doi.org/10.2307/2261605openalex-snapshot
On Misinterpreting the `Phylogenetic Correction'
inferredcites →https://doi.org/10.2307/2261640openalex-snapshot
Further Remarks on Phylogenetic Correction
inferredcites →https://doi.org/10.2307/2389354openalex-snapshot
Basal Metabolic Rates in Mammals: Allometry, Phylogeny and Ecology
inferredcites →https://doi.org/10.2307/3545598openalex-snapshot
Applications of Phylogenetically Independent Contrasts: A Mixed Progress Report
inferredcites →https://doi.org/10.2307/3546637openalex-snapshot
Are 'Comparative Methods' Always Necessary?
inferredcites →https://doi.org/10.2307/3676282openalex-snapshot
Growth and Development of Heat Regulation in Nestlings, and Metabolism of Adult Common and Thick-Billed Murres
inferredcites →https://doi.org/10.2307/3677098openalex-snapshot
Basal Metabolic Rates of Migrating Waders in the Eurasian Arctic
inferredcites →https://doi.org/10.2307/3677259openalex-snapshot
Seasonal Variation in Cold Tolerance, Basal Metabolic Rate, and Maximal Capacity for Thermogenesis in White-Breasted Nuthatches Sitta carolinensis and Downy Woodpeckers Picoides pubescens, Two Unrelated Arboreal Temperate Residents
inferredcites →https://doi.org/10.2307/3677350openalex-snapshot
Migration-Induced Variation in Thermogenic Capacity in Migratory Passerines
inferredcites →https://doi.org/10.2307/4083408openalex-snapshot
Some Aspects of Temperature Relations in Small Owls
inferredcites →https://doi.org/10.2307/4086838openalex-snapshot
Basal Metabolic Rate in Tropical Seabirds
inferredcites →https://doi.org/10.2307/4089034openalex-snapshot
Maximum Metabolic Rate, Thermal Insulation and Aerobic Scope in a Small-Sized Chilean Hummingbird (Sephanoides sephanoides)
inferredcites →https://doi.org/10.2307/4089429openalex-snapshot
Metabolic Rate, Temperature Regulation, and the Energetic Implications of Roost Nests in the Bananaquit (Coereba flaveola)
inferredcites →https://doi.org/10.2307/4089474openalex-snapshot
Maintenance Energy Costs of Two Partially Folivorous Tropical Passerines
inferredcites →https://doi.org/10.3382/ps.0190239openalex-snapshot
Seasonal Metabolic Rhythms in the Domestic Fowl
inferredcites →https://doi.org/10.5253/arde.v72.p1openalex-snapshot
Ecological Energetics of the Long-Eared Owl (Asio Otus)
inferredcites →https://doi.org/10.5253/arde.v75.p175openalex-snapshot
High Levels of Energy Expenditure in Shorebirds; Metabolic Adaptations to an Energetically Expensive Way of Life
inferredcites →https://doi.org/10.5281/zenodo.16089485openalex-snapshot
Metabolic Rate and Evaporative Water Loss of Mexican Spotted and Great Horned Owls
inferredcites →https://doi.org/10.5281/zenodo.16376646openalex-snapshot
Standard Metabolic Rate and Lower Critical Temperature for the Ruffed Grouse
inferredcites →https://doi.org/10.5860/choice.29-5104openalex-snapshot
The comparative method in evolutionary biology
inferredcites →https://doi.org/10.5962/bhl.title.34390openalex-snapshot
The influence of distribution and ecology on the thermoregulation of small birds
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.6620/zs.2019.58-06zenodo-depositor-declared
Physiological and Biochemical Thermoregulatory Responses in Male Chinese Hwameis to Seasonal Acclimatization: Phenotypic Flexibility in a Small Passerine.
inferred← citeshttps://doi.org/10.1002/cphy.c100079openalex-snapshot
Phylogenetic Analyses: Comparing Species to Infer Adaptations and Physiological Mechanisms
inferred← citeshttps://doi.org/10.1002/cphy.c110049openalex-snapshot
Metabolic Scaling in Animals: Methods, Empirical Results, and Theoretical Explanations
inferred← citeshttps://doi.org/10.1002/cphy.c130032openalex-snapshot
Metabolism at the Max: How Vertebrate Organisms Respond to Physical Activity
inferred← citeshttps://doi.org/10.1002/cphy.c220003openalex-snapshot
The Mouse‐To‐Elephant Metabolic Curve: Historical Overview
inferred← citeshttps://doi.org/10.1002/ecy.4206openalex-snapshot
Equivocal support for the climate variability hypothesis within a N eotropical bird assemblage
inferred← citeshttps://doi.org/10.1002/ecy.4279openalex-snapshot
Evolution of avian heat tolerance: The role of atmospheric humidity
inferred← citeshttps://doi.org/10.1002/j.2040-4603.2012.tb00401.xopenalex-snapshot
Phylogenetic Analyses: Comparing Species to Infer Adaptations and Physiological Mechanisms
inferred← citeshttps://doi.org/10.1002/j.2040-4603.2014.tb00540.xopenalex-snapshot
Metabolic Scaling in Animals: Methods, Empirical Results, and Theoretical Explanations
inferred← citeshttps://doi.org/10.1002/j.2040-4603.2015.tb00654.xopenalex-snapshot
Metabolism at the Max: How Vertebrate Organisms Respond to Physical Activity
inferred← citeshttps://doi.org/10.1002/j.2040-4603.2023.tb00258.xopenalex-snapshot
The Mouse‐To‐Elephant Metabolic Curve: Historical Overview
inferred← citeshttps://doi.org/10.1002/jmor.20053openalex-snapshot
Scaling of the ballistic tongue apparatus in chameleons
inferred← citeshttps://doi.org/10.1007/978-1-4419-6421-2_3openalex-snapshot
Seasonal Metabolic Variation in Birds: Functional and Mechanistic Correlates
inferred← citeshttps://doi.org/10.1007/978-3-031-35180-8_4openalex-snapshot
Function of the Avian Respiratory System
inferred← citeshttps://doi.org/10.1007/s00244-016-0288-2openalex-snapshot
Trace Elements in Sea Ducks of the Alaskan Arctic Coast: Patterns of Variation Among Species, Sexes, and Ages
inferred← citeshttps://doi.org/10.1007/s00360-007-0218-8openalex-snapshot
Phenotypic flexibility in basal metabolic rate and the changing view of avian physiological diversity: a review
inferred← citeshttps://doi.org/10.1007/s00360-011-0590-2openalex-snapshot
The allometry of parrot BMR: seasonal data for the Greater Vasa Parrot, Coracopsis vasa, from Madagascar
inferred← citeshttps://doi.org/10.1007/s00360-012-0676-5openalex-snapshot
Determinants of inter-specific variation in basal metabolic rate
inferred← citeshttps://doi.org/10.1007/s00360-014-0850-zopenalex-snapshot
Behavioral and ecological factors account for variation in the mass-independent energy expenditures of endotherms
inferred← citeshttps://doi.org/10.1007/s00360-016-0964-6openalex-snapshot
A ‘slow pace of life’ in Australian old-endemic passerine birds is not accompanied by low basal metabolic rates
inferred← citeshttps://doi.org/10.1007/s00360-020-01322-0openalex-snapshot
Phenotypic flexibility in heat production and heat loss in response to thermal and hydric acclimation in the zebra finch, a small arid-zone passerine
inferred← citeshttps://doi.org/10.1007/s00411-010-0302-4openalex-snapshot
Energy metabolism used as a tool to model the transfer of 14C and 3H in animals
inferred← citeshttps://doi.org/10.1007/s00442-006-0522-0openalex-snapshot
Correlation of metabolism with tissue carbon and nitrogen turnover rate in small mammals
inferred← citeshttps://doi.org/10.1007/s10336-007-0186-5openalex-snapshot
Avian senescence: underlying mechanisms
inferred← citeshttps://doi.org/10.1007/s10336-021-01915-8openalex-snapshot
Essential amino acid requirements of granivorous and omnivorous songbirds and the provision of natural foods
inferred← citeshttps://doi.org/10.1007/s10336-022-01962-9openalex-snapshot
A trait-based approach to seasonal dynamics of an alpine and subalpine passerine bird assemblage
inferred← citeshttps://doi.org/10.1007/s10336-026-02380-xopenalex-snapshot
Seasonal dynamics of urban bird communities: impact of habitat on breeding and wintering bird communities in a northern temperate region
inferred← citeshttps://doi.org/10.1007/s11284-014-1182-xopenalex-snapshot
The intraspecies relationship between tissue turnover and metabolic rate in rats
inferred← citeshttps://doi.org/10.1007/s11538-008-9382-6openalex-snapshot
Evolutionary Entropy: A Predictor of Body Size, Metabolic Rate and Maximal Life Span
inferred← citeshttps://doi.org/10.1016/b978-0-12-819770-7.00025-6openalex-snapshot
Regulation of body temperature
inferred← citeshttps://doi.org/10.1016/b978-0-7234-3832-8.00003-1openalex-snapshot
Nutrition and Nutritional Management
inferred← citeshttps://doi.org/10.1016/j.actao.2007.12.001openalex-snapshot
Geographic differences between functional groups in patterns of bird species richness in North America
inferred← citeshttps://doi.org/10.1016/j.actao.2023.103889openalex-snapshot
On the natural selection of body mass allometries
inferred← citeshttps://doi.org/10.1016/j.bone.2013.08.010openalex-snapshot
Measurement, variation, and scaling of osteocyte lacunae: a case study in birds
inferred← citeshttps://doi.org/10.1016/j.cbpa.2005.07.013openalex-snapshot
Sample size and mass range effects on the allometric exponent of basal metabolic rate
inferred← citeshttps://doi.org/10.1016/j.cbpa.2005.09.019openalex-snapshot
Allometric estimation of metabolic rate from heart rate in penguins
inferred← citeshttps://doi.org/10.1016/j.cbpa.2006.03.018openalex-snapshot
Development of maximum metabolic rate and pulmonary diffusing capacity in the superprecocial Australian Brush Turkey Alectura lathami: An allometric and morphometric study
inferred← citeshttps://doi.org/10.1016/j.cbpa.2007.08.007openalex-snapshot
Time–activity budgets and energetics of Dipper Cinclus cinclus are dictated by temporal variability of river flow
inferred← citeshttps://doi.org/10.1016/j.cbpa.2008.04.599openalex-snapshot
Short-term thermoregulatory adjustments in a South American anseriform, the black-necked swan (Cygnus melanocoryphus)
inferred← citeshttps://doi.org/10.1016/j.cbpa.2008.05.008openalex-snapshot
An analysis of the factors that influence the level and scaling of mammalian BMR
inferred← citeshttps://doi.org/10.1016/j.cbpa.2008.07.009openalex-snapshot
Seasonal acclimatization of metabolism in Eurasian tree sparrows (Passer montanus)
inferred← citeshttps://doi.org/10.1016/j.cbpa.2008.08.021openalex-snapshot
Ecological factors affect the level and scaling of avian BMR
inferred← citeshttps://doi.org/10.1016/j.cbpa.2009.08.019openalex-snapshot
Seasonal variation in energy expenditure and body composition in captive White Storks (Ciconia ciconia)
inferred← citeshttps://doi.org/10.1016/j.cbpa.2010.07.018openalex-snapshot
Metabolic rate and specific dynamic action of the Red-legged Honeycreeper,a nectar-feeding Neotropical passerine
inferred← citeshttps://doi.org/10.1016/j.cbpa.2010.10.004openalex-snapshot
Allometric estimation of metabolic rates in animals
inferred← citeshttps://doi.org/10.1016/j.cbpa.2012.12.004openalex-snapshot
Geographic variation in basal thermogenesis in little buntings: Relationship to cellular thermogenesis and thyroid hormone concentrations
inferred← citeshttps://doi.org/10.1016/j.cbpa.2014.07.009openalex-snapshot
Cellular metabolic rates from primary dermal fibroblast cells isolated from birds of different body masses
inferred← citeshttps://doi.org/10.1016/j.cbpa.2014.07.026openalex-snapshot
How do measurement duration and timing interact to influence estimation of basal physiological variables of a nocturnal rodent?
inferred← citeshttps://doi.org/10.1016/j.cbpa.2014.09.026openalex-snapshot
Seasonal variation in body mass, body temperature and thermogenesis in the Hwamei, Garrulax canorus
inferred← citeshttps://doi.org/10.1016/j.cbpa.2015.10.005openalex-snapshot
Avian energetics: The passerine/non-passerine dichotomy
inferred← citeshttps://doi.org/10.1016/j.cbpa.2016.02.023openalex-snapshot
Physiological constraints and dive behavior scale in tandem with body mass in auks: A comparative analysis
inferred← citeshttps://doi.org/10.1016/j.cbpa.2016.07.013openalex-snapshot
The increase in fat content in the warm-acclimated striped hamsters is associated with the down-regulated metabolic thermogenesis
inferred← citeshttps://doi.org/10.1016/j.cbpa.2019.06.003openalex-snapshot
Flight costs in volant vertebrates: A phylogenetically-controlled meta-analysis of birds and bats
inferred← citeshttps://doi.org/10.1016/j.cbpa.2019.110541openalex-snapshot
Reassessing the definition of basal metabolic rate: Circadian considerations in avian studies
inferred← citeshttps://doi.org/10.1016/j.cbpa.2024.111688openalex-snapshot
Reporting guidelines for terrestrial respirometry: Building openness, transparency of metabolic rate and evaporative water loss data
inferred← citeshttps://doi.org/10.1016/j.chnaes.2010.11.013openalex-snapshot
Seasonal changes of thermogenic capacity in Melano-bellied oriental voles (Eothenomys melanogaster)
inferred← citeshttps://doi.org/10.1016/j.cub.2025.05.025openalex-snapshot
Energy conversion efficiency peaks at intermediate flight speed in a migratory songbird
inferred← citeshttps://doi.org/10.1016/j.ecoinf.2024.102492openalex-snapshot
Population dynamic life history models of the birds and mammals of the world
inferred← citeshttps://doi.org/10.1016/j.ecolmodel.2018.04.001openalex-snapshot
Temperature-influenced energetics model for migrating waterfowl
inferred← citeshttps://doi.org/10.1016/j.imr.2016.01.002openalex-snapshot
A model for allometric scaling of mammalian metabolism with ambient heat loss
inferred← citeshttps://doi.org/10.1016/j.isci.2023.107743openalex-snapshot
Biophysical models accurately characterize the thermal energetics of a small invasive passerine bird
inferred← citeshttps://doi.org/10.1016/j.jhevol.2006.03.006openalex-snapshot
Costs of encephalization: the energy trade-off hypothesis tested on birds
inferred← citeshttps://doi.org/10.1016/j.jtherbio.2007.11.001openalex-snapshot
Thermoregulatory responses in seasonally acclimatized captive Southern White-faced Scops-owls
inferred← citeshttps://doi.org/10.1016/j.jtherbio.2008.03.003openalex-snapshot
Seasonal variation on metabolism and thermoregulation in Chinese bulbul
inferred← citeshttps://doi.org/10.1016/j.jtherbio.2008.06.005openalex-snapshot
Seasonal effects on thermoregulatory responses of the Rock Kestrel, Falco rupicolis
inferred← citeshttps://doi.org/10.1016/j.jtherbio.2010.05.002openalex-snapshot
Remote sensing of physiological data: Impact of long term captivity on body temperature variation of the feral cat (Felis catus) in Australia, recorded via Thermochron iButtons
inferred← citeshttps://doi.org/10.1016/j.jtherbio.2010.06.010openalex-snapshot
The link between metabolic rate and body temperature in galliform birds in thermoneutral and heat exposure conditions: The classical and phylogenetically corrected approach
inferred← citeshttps://doi.org/10.1016/j.jtherbio.2011.07.007openalex-snapshot
Does use of the torpor cut-off method to analyze variation in body temperature cause more problems than it solves?
inferred← citeshttps://doi.org/10.1016/j.jtherbio.2011.08.001openalex-snapshot
Baby in the bathwater: Should we abandon the use of body temperature thresholds to quantify expression of torpor?
inferred← citeshttps://doi.org/10.1016/j.jtherbio.2012.06.004openalex-snapshot
Is respirometry a standardized technique? A review of measurement of avian resting metabolic rates
inferred← citeshttps://doi.org/10.1016/j.jtherbio.2013.10.003openalex-snapshot
Metabolic thermogenesis and evaporative water loss in the Hwamei Garrulax canorus
inferred← citeshttps://doi.org/10.1016/j.jtherbio.2022.103197openalex-snapshot
The seasonal variation of basal metabolic rate is related to the expression of torpor among small mammals
inferred← citeshttps://doi.org/10.1016/j.mad.2007.11.001openalex-snapshot
Intra-specific variation in resting metabolic rate in MF1 mice is not associated with membrane lipid desaturation in the liver
inferred← citeshttps://doi.org/10.1016/j.plrev.2006.08.001openalex-snapshot
Allometric scaling laws of metabolism
inferred← citeshttps://doi.org/10.1016/j.resp.2008.07.015openalex-snapshot
Cost of growth and maintenance in chicken embryos during normoxic or hypoxic conditions
inferred← citeshttps://doi.org/10.1017/s0954102012001149openalex-snapshot
Persistent organic pollutants in bird, fish and invertebrate samples from King George Island, Antarctica
inferred← citeshttps://doi.org/10.1017/s1464793105006834openalex-snapshot
Beyond the ‘3/4‐power law’: variation in the intra‐and interspecific scaling of metabolic rate in animals
inferred← citeshttps://doi.org/10.1021/acs.est.2c02177openalex-snapshot
Biomagnification of Persistent Organic Pollutants from Terrestrial and Aquatic Invertebrates to Songbirds: Associations with Physiochemical and Ecological Indicators
inferred← citeshttps://doi.org/10.1038/s41467-018-05898-8openalex-snapshot
Reflection of near-infrared light confers thermal protection in birds
inferred← citeshttps://doi.org/10.1038/s41559-023-02307-2openalex-snapshot
Shrinking body size may not provide meaningful thermoregulatory benefits in a warmer world
inferred← citeshttps://doi.org/10.1038/s41598-024-67222-3openalex-snapshot
Contrasting morphometric responses to increasing urbanisation in congeneric sparrow species
inferred← citeshttps://doi.org/10.1038/srep18625openalex-snapshot
Off like a shot: scaling of ballistic tongue projection reveals extremely high performance in small chameleons
inferred← citeshttps://doi.org/10.1071/ea08142openalex-snapshot
Thermoregulation in ratites: a review
inferred← citeshttps://doi.org/10.1073/pnas.0702212104openalex-snapshot
Tropical birds have a slow pace of life
inferred← citeshttps://doi.org/10.1073/pnas.0707683104openalex-snapshot
Cold- and exercise-induced peak metabolic rates in tropical birds
inferred← citeshttps://doi.org/10.1073/pnas.1907360117openalex-snapshot
Physical limits of flight performance in the heaviest soaring bird
inferred← citeshttps://doi.org/10.1073/pnas.2116645119openalex-snapshot
Adaptive variation in the upper limits of avian body temperature
inferred← citeshttps://doi.org/10.1073/pnas.2216016120openalex-snapshot
Long-duration wind tunnel flights reveal exponential declines in protein catabolism over time in short- and long-distance migratory warblers
inferred← citeshttps://doi.org/10.1080/03014223.2016.1148746openalex-snapshot
Analysis of factors that influence energy expenditure in honeyeaters (Meliphagidae)
inferred← citeshttps://doi.org/10.1080/08912961003787598openalex-snapshot
Giants on the landscape: modelling the abundance of megaherbivorous dinosaurs of the Morrison Formation (Late Jurassic, western USA)
inferred← citeshttps://doi.org/10.1086/501063openalex-snapshot
Environmental Correlates of Physiological Variables in Marsupials
inferred← citeshttps://doi.org/10.1086/502814openalex-snapshot
Allometry, Antilog Transformations, and the Perils of Prediction on the Original Scale
inferred← citeshttps://doi.org/10.1086/523318openalex-snapshot
Behavioral and Physiological Significance of Minimum Resting Metabolic Rate in King Penguins
inferred← citeshttps://doi.org/10.1086/527491openalex-snapshot
The Scaling of Diving Time Budgets: Insights from an Optimality Approach
inferred← citeshttps://doi.org/10.1086/589456openalex-snapshot
Interspecific Associations between Circulating Antioxidant Levels and Life‐History Variation in Birds
inferred← citeshttps://doi.org/10.1086/590222openalex-snapshot
Intrapopulation Variation in the Standard Metabolism of a Terrestrial Mollusc: Repeatability of the CO2Production in the Land SnailHelix aspersa
inferred← citeshttps://doi.org/10.1086/592821openalex-snapshot
Modeling the Marine Resources Consumed in Raising a King Penguin Chick: An Energetics Approach
inferred← citeshttps://doi.org/10.1086/605336openalex-snapshot
Low Metabolism and Inactive Lifestyle of a Tropical Rain Forest Bird Investigated via Heart‐Rate Telemetry
inferred← citeshttps://doi.org/10.1086/647904openalex-snapshot
Insect Rate‐Temperature Relationships: Environmental Variation and the Metabolic Theory of Ecology
inferred← citeshttps://doi.org/10.1086/651564openalex-snapshot
A New Model for the Body Size–Metabolism Relationship
inferred← citeshttps://doi.org/10.1086/658084openalex-snapshot
Basal Metabolic Rate of Endotherms Can Be Modeled Using Heat-Transfer Principles and Physiological Concepts: Reply to “Can the Basal Metabolic Rate of Endotherms Be Explained by Biophysical Modeling?”
inferred← citeshttps://doi.org/10.1086/676832openalex-snapshot
Seasonal Variation of Metabolic Thermogenesis in Eurasian Tree Sparrows (Passer montanus) over a Latitudinal Gradient
inferred← citeshttps://doi.org/10.1086/676933openalex-snapshot
Experimental Sources of Variation in Avian Energetics: Estimated Basal Metabolic Rate Decreases with Successive Measurements
inferred← citeshttps://doi.org/10.1086/682700openalex-snapshot
The (Mostly) Good, the (Few) Bad, and the (Couple of) Ugly Chapters inSturkie’s Avian PhysiologySturkie’s Avian Physiology. Edited by Colin G. Scanes. Waltham, MA: Academic Press, 2014. ISBN 978-0-124-07160-5.
inferred← citeshttps://doi.org/10.1086/685411openalex-snapshot
Basal Metabolic Rate of the Black-Faced Sheathbill (Chionis minor): Intraspecific Variation in a Phylogenetically Distinct Island Endemic
inferred← citeshttps://doi.org/10.1086/686716openalex-snapshot
Reexamining Echidna Physiology: The Big Picture forTachyglossus aculeatus acanthion
inferred← citeshttps://doi.org/10.1086/692326openalex-snapshot
The Evolution of Energetic Scaling across the Vertebrate Tree of Life
inferred← citeshttps://doi.org/10.1086/714018openalex-snapshot
Using Integrative Biology to Infer Adaptation from Comparisons of Two (or a Few) Species
inferred← citeshttps://doi.org/10.1086/736561openalex-snapshot
Insensible Evaporative Water Loss Control by an Australian Arid-Habitat Psittacine, the Mulga Parrot (Psephotellus varius)
inferred← citeshttps://doi.org/10.1086/737777openalex-snapshot
Migratory Birds on Wintering Grounds in Tropics Have a Higher Basal Metabolic Rate than Tropical Residents
inferred← citeshttps://doi.org/10.1093/auk/ukz069openalex-snapshot
Environmental determinants of total evaporative water loss in birds at multiple temperatures
inferred← citeshttps://doi.org/10.1093/beheco/araf073openalex-snapshot
Behavior across time and space – how large scale “trait-based” approaches can shape behavioral ecology
inferred← citeshttps://doi.org/10.1093/condor/108.1.166openalex-snapshot
The Allometric Relationship between Resting Metabolic Rate and Body Mass in Wild Waterfowl (Anatidae) and an Application to Estimation of Winter Habitat Requirements
inferred← citeshttps://doi.org/10.1093/conphys/coaa048openalex-snapshot
Avian mortality risk during heat waves will increase greatly in arid Australia during the 21st century
inferred← citeshttps://doi.org/10.1093/conphys/cox058openalex-snapshot
Reduced metabolic rate indicates declining viability in seed collections: an experimental proof-of-concept
inferred← citeshttps://doi.org/10.1093/cz/zox018openalex-snapshot
Basal metabolic rate in free-living tropical birds: the influence of phylogenetic, behavioral, and ecological factors
inferred← citeshttps://doi.org/10.1093/czoolo/56.6.741openalex-snapshot
Sources and significance of variation in basal, summit and maximal metabolic rates in birds
inferred← citeshttps://doi.org/10.1093/gerona/62.2.149openalex-snapshot
An Analysis of the Relationship Between Metabolism, Developmental Schedules, and Longevity Using Phylogenetic Independent Contrasts
inferred← citeshttps://doi.org/10.1093/icb/icu035openalex-snapshot
Testing Hypotheses in Ecoimmunology Using Mixed Models: Disentangling Hierarchical Correlations
inferred← citeshttps://doi.org/10.1093/icb/icz017openalex-snapshot
Does Cellular Metabolism from Primary Fibroblasts and Oxidative Stress in Blood Differ between Mammals and Birds? The (Lack-thereof) Scaling of Oxidative Stress
inferred← citeshttps://doi.org/10.1098/rsbl.2005.0378openalex-snapshot
The scaling and temperature dependence of vertebrate metabolism
inferred← citeshttps://doi.org/10.1098/rsbl.2006.0538openalex-snapshot
Metabolic costs of brain size evolution
inferred← citeshttps://doi.org/10.1098/rsbl.2009.0691openalex-snapshot
Group-foraging is not associated with longevity in North American birds
inferred← citeshttps://doi.org/10.1098/rsbl.2026.0055openalex-snapshot
Migrating by night, inactive by day: ecological barrier crossing in a migratory songbird
inferred← citeshttps://doi.org/10.1098/rspb.2005.3415openalex-snapshot
Phenotypic plasticity in the scaling of avian basal metabolic rate
inferred← citeshttps://doi.org/10.1098/rspb.2006.3727openalex-snapshot
Basal metabolic rate of birds is associated with habitat temperature and precipitation, not primary productivity
inferred← citeshttps://doi.org/10.1098/rspb.2008.0118openalex-snapshot
Effects of metabolic level on the body size scaling of metabolic rate in birds and mammals
inferred← citeshttps://doi.org/10.1098/rspb.2008.1012openalex-snapshot
Genome size and wing parameters in passerine birds
inferred← citeshttps://doi.org/10.1098/rspb.2012.0884openalex-snapshot
An information-theoretic approach to evaluating the size and temperature dependence of metabolic rate
inferred← citeshttps://doi.org/10.1098/rspb.2017.0232openalex-snapshot
Global patterns of thermal tolerances and vulnerability of endotherms to climate change remain robust irrespective of varying data suitability criteria
inferred← citeshttps://doi.org/10.1098/rspb.2020.2348openalex-snapshot
Aminopeptidase-N modulation assists lean mass anabolism during refuelling in the white-throated sparrow
inferred← citeshttps://doi.org/10.1098/rspb.2023.1251openalex-snapshot
Endotherms trade body temperature regulation for the stress response
inferred← citeshttps://doi.org/10.1098/rspb.2024.2489openalex-snapshot
The hummingbird’s adipostat: can a simple rule explain torpor frequency and duration in hummingbirds?
inferred← citeshttps://doi.org/10.1098/rspb.2024.2683openalex-snapshot
Metabolic rate of angiosperm seeds: effects of allometry, phylogeny and bioclimate
inferred← citeshttps://doi.org/10.1101/188656openalex-snapshot
A whole genome analysis of the red-crowned crane provides insight into avian longevity
inferred← citeshttps://doi.org/10.1101/694067openalex-snapshot
Scaling of organ masses in mammals and birds: phylogenetic signal and implications for metabolic rate scaling
inferred← citeshttps://doi.org/10.1111/1365-2435.12348openalex-snapshot
Basal metabolism in tropical birds: latitude, altitude, and the ‘pace of life’
inferred← citeshttps://doi.org/10.1111/1365-2435.13152openalex-snapshot
Diet complementation as a frequency‐dependent mechanism conferring advantages to rare plants via dispersal
inferred← citeshttps://doi.org/10.1111/1365-2435.13230openalex-snapshot
Non‐invasive measurement of metabolic rates in wild, free‐living birds using doubly labelled water
inferred← citeshttps://doi.org/10.1111/1365-2435.13238openalex-snapshot
Fuel for the pace of life: Baseline blood glucose concentration co‐evolves with life‐history traits in songbirds
inferred← citeshttps://doi.org/10.1111/1365-2435.13526openalex-snapshot
Environmental and ecological correlates of avian field metabolic rate and water flux
inferred← citeshttps://doi.org/10.1111/1365-2435.13693openalex-snapshot
Heat tolerances of temperate and tropical birds and their implications for susceptibility to climate warming
inferred← citeshttps://doi.org/10.1111/1365-2656.70162openalex-snapshot
Sweat the small stuff: A review of the use of accelerometers to estimate energy expenditure in wild animals
inferred← citeshttps://doi.org/10.1111/brv.12350openalex-snapshot
Comparative analyses of basal rate of metabolism in mammals: data selection does matter
inferred← citeshttps://doi.org/10.1111/ecog.01465openalex-snapshot
Disentangling environmental drivers of metabolic flexibility in birds: the importance of temperature extremes versus temperature variability
inferred← citeshttps://doi.org/10.1111/ele.13464openalex-snapshot
Metabolic rate is negatively linked to adult survival but does not explain latitudinal differences in songbirds
inferred← citeshttps://doi.org/10.1111/ele.14525openalex-snapshot
Territory Sizes and Patterns of Habitat Use by Forest Birds Over Five Decades: Ideal Free or Ideal Despotic?
inferred← citeshttps://doi.org/10.1111/geb.13069openalex-snapshot
No evidence for the ‘rate‐of‐living’ theory across the tetrapod tree of life
inferred← citeshttps://doi.org/10.1111/ivb.12199openalex-snapshot
Metabolic scaling in modular animals
inferred← citeshttps://doi.org/10.1111/j.0908-8857.2007.03774.xopenalex-snapshot
Seasonal sex–specific energy expenditure in breeding and non-breeding Palestine sunbirds Nectarinia osea
inferred← citeshttps://doi.org/10.1111/j.0908-8857.2008.04427.xopenalex-snapshot
Daily energy expenditure of singing great reed warblers Acrocephalus arundinaceus
inferred← citeshttps://doi.org/10.1111/j.1365-2435.2006.01170.xopenalex-snapshot
A comparative analysis of the diving behaviour of birds and mammals
inferred← citeshttps://doi.org/10.1111/j.1365-2435.2007.01245.xopenalex-snapshot
Scaling of insect metabolic rate is inconsistent with the nutrient supply network model
inferred← citeshttps://doi.org/10.1111/j.1365-2435.2007.01371.xopenalex-snapshot
Scaling metabolic rate with body mass and inverse body temperature: a test of the Arrhenius fractal supply model
inferred← citeshttps://doi.org/10.1111/j.1365-2435.2008.01399.xopenalex-snapshot
Allometric scaling of maximum metabolic rate: the influence of temperature
inferred← citeshttps://doi.org/10.1111/j.1365-2435.2009.01583.xopenalex-snapshot
Metabolic level and size scaling of rates of respiration and growth in unicellular organisms
inferred← citeshttps://doi.org/10.1111/j.1365-2435.2009.01599.xopenalex-snapshot
Ecological and physiological determinants of dive duration in the freshwater crocodile
inferred← citeshttps://doi.org/10.1111/j.1365-2656.2006.01127.xopenalex-snapshot
Moving towards acceleration for estimates of activity‐specific metabolic rate in free‐living animals: the case of the cormorant
inferred← citeshttps://doi.org/10.1111/j.1365-2699.2007.01772.xopenalex-snapshot
Ecogeographical rules: elements of a synthesis
inferred← citeshttps://doi.org/10.1111/j.1365-2869.2006.00559.xopenalex-snapshot
A phylogenetic analysis of the correlates of sleep in birds
inferred← citeshttps://doi.org/10.1111/j.1365-3032.2009.00714.xopenalex-snapshot
Scaling of metabolic rate in the lesser wax moth Achroia grisella does not fit the 3/4‐power law and shows significant sex differences
inferred← citeshttps://doi.org/10.1111/j.1420-9101.2009.01783.xopenalex-snapshot
A database of vertebrate longevity records and their relation to other life‐history traits
inferred← citeshttps://doi.org/10.1111/j.1439-0396.2007.00791.xopenalex-snapshot
Symmorphosis and livestock bioenergetics: production animal muscle has low mitochondrial volume fractions
inferred← citeshttps://doi.org/10.1111/j.1466-8238.2008.00388.xopenalex-snapshot
Environmental factors, regional body size distributions and spatial variation in body size of local avian assemblages
inferred← citeshttps://doi.org/10.1111/j.1469-185x.2009.00095.xopenalex-snapshot
A unifying explanation for diverse metabolic scaling in animals and plants
inferred← citeshttps://doi.org/10.1111/j.1469-7998.2006.00138.xopenalex-snapshot
Physiological correlates of habitat association in East African sunbirds (Nectariniidae)
inferred← citeshttps://doi.org/10.1111/j.1558-5646.2008.00522.xopenalex-snapshot
THE EVOLUTION OF HIGH SUMMIT METABOLISM AND COLD TOLERANCE IN BIRDS AND ITS IMPACT ON PRESENT-DAY DISTRIBUTIONS
inferred← citeshttps://doi.org/10.1111/j.1558-5646.2009.00747.xopenalex-snapshot
PHYLOGENETICALLY INFORMED ANALYSIS OF THE ALLOMETRY OF MAMMALIAN BASAL METABOLIC RATE SUPPORTS NEITHER GEOMETRIC NOR QUARTER-POWER SCALING
inferred← citeshttps://doi.org/10.1111/j.1600-048x.2013.00126.xopenalex-snapshot
Antioxidant status in relation to age, condition, reproductive performance and pollution in three passerine species
inferred← citeshttps://doi.org/10.1111/j.1600-048x.2013.05869.xopenalex-snapshot
Metabolic response to changes in temperature in northern wheatears from an arctic and a temperate populations
inferred← citeshttps://doi.org/10.1111/j.1744-7429.2006.00216.xopenalex-snapshot
Energetics of East African Pycnonotids1
inferred← citeshttps://doi.org/10.1111/j.1749-4877.2012.00287.xopenalex-snapshot
Direct impacts of climatic warming on heat stress in endothermic species: seabirds as bioindicators of changing thermoregulatory constraints
inferred← citeshttps://doi.org/10.1111/j.2007.0908-8857.03774.xopenalex-snapshot
Seasonal sex–specific energy expenditure in breeding and non‐breeding Palestine sunbirds Nectarinia osea
inferred← citeshttps://doi.org/10.1111/jav.02067openalex-snapshot
Differences between temperate and tropical birds in seasonal acclimatization of thermoregulatory traits
inferred← citeshttps://doi.org/10.1111/jbi.13068openalex-snapshot
Phylogenetic signals in thermal traits remain stronger in the tropics if we can believe published physiological data. A reply to McKechnie et al., “Data quality problems undermine analyses of endotherm upper critical temperatures”
inferred← citeshttps://doi.org/10.1111/jzo.13029openalex-snapshot
Macrophysiology for decision‐making
inferred← citeshttps://doi.org/10.1111/pala.12583openalex-snapshot
Palaeohistological inferences of resting metabolic rates inConcornisandIberomesornis(Enantiornithes, Ornithothoraces) from the Lower Cretaceous of Las Hoyas (Spain)
inferred← citeshttps://doi.org/10.1121/1.5005495openalex-snapshot
Allometric trends reveal distinct evolutionary trajectories for avian communication
inferred← citeshttps://doi.org/10.1126/science.1253143openalex-snapshot
Evidence for mesothermy in dinosaurs
inferred← citeshttps://doi.org/10.1134/s1062359012080055openalex-snapshot
Fundamental avian energetics: 2. The ability of birds to change heat loss and explanation of the mass exponent for basal metabolism in homeothermic animals
inferred← citeshttps://doi.org/10.1139/z07-051openalex-snapshot
Establishing elemental turnover in exercising birds using a wind tunnel: implications for stable isotope tracking of migrants
inferred← citeshttps://doi.org/10.1152/physiol.00015.2023openalex-snapshot
How and Why Does Metabolism Scale with Body Mass?
inferred← citeshttps://doi.org/10.1152/physrev.00047.2006openalex-snapshot
Life and Death: Metabolic Rate, Membrane Composition, and Life Span of Animals
inferred← citeshttps://doi.org/10.11606/t.21.2011.tde-20042012-095950openalex-snapshot
Poluentes orgânicos e isótopos estáveis no ecossistema da Baía do Almirantado, Ilha Rei George, Antártida
inferred← citeshttps://doi.org/10.1186/s40657-015-0011-4openalex-snapshot
Daily variation in body mass and thermoregulation in male Hwamei (Garrulax canorus) at different seasons
inferred← citeshttps://doi.org/10.1186/s40657-017-0083-4openalex-snapshot
Seasonal phenotypic flexibility in body mass, basal thermogenesis, and tissue oxidative capacity in the male Silky Starling (Sturnus sericeus)
inferred← citeshttps://doi.org/10.1186/s40657-018-0131-8openalex-snapshot
Food restriction decreases BMR, body and organ mass, and cellular energetics, in the Chinese Bulbul (Pycnonotus sinensis)
inferred← citeshttps://doi.org/10.1186/s40665-016-0027-yopenalex-snapshot
An estimate of the water budget for the endangered night parrot of Australia under recent and future climates
inferred← citeshttps://doi.org/10.1242/jeb.01501openalex-snapshot
Allometric scaling of mammalian metabolism
inferred← citeshttps://doi.org/10.1242/jeb.01745openalex-snapshot
Phylogenetic approaches in comparative physiology
inferred← citeshttps://doi.org/10.1242/jeb.02362openalex-snapshot
A critical understanding of the fractal model of metabolic scaling
inferred← citeshttps://doi.org/10.1242/jeb.02724openalex-snapshot
Characterization of very-low density lipoprotein particle diameter dynamics in relation to egg production in a passerine bird
inferred← citeshttps://doi.org/10.1242/jeb.055046openalex-snapshot
Aerobic capacity in wild satin bowerbirds: repeatability and effects of age, sex and condition
inferred← citeshttps://doi.org/10.1242/jeb.088914openalex-snapshot
Phylogenetic analysis of mammalian maximal oxygen consumption during exercise
inferred← citeshttps://doi.org/10.1242/jeb.108894openalex-snapshot
Ways to be different: foraging adaptations that facilitate higher intake rates in a northerly-wintering shorebird compared to a low-latitude conspecific
inferred← citeshttps://doi.org/10.1242/jeb.144972openalex-snapshot
Energetics of communal roosting in chestnut-crowned babblers: implications for group dynamics and breeding phenology
inferred← citeshttps://doi.org/10.1242/jeb.171108openalex-snapshot
Avian thermoregulation in the heat: metabolism, evaporative cooling and gular flutter in two small owls
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