| review article | Q7318358 |
| scholarly article | Q13442814 |
| P2093 | author name string | Tony D Williams | |
| P2860 | cites work | Selection Experiments as a Tool in Evolutionary and Comparative Physiology: Insights into Complex Traits--an Introduction to the Symposium | Q22066038 |
| Phylogenetic approaches in comparative physiology | Q28265799 | ||
| Evolution of a polyphenism by genetic accommodation | Q28295324 | ||
| Superspreading and the effect of individual variation on disease emergence | Q29618989 | ||
| Hormone-mediated suites as adaptations and evolutionary constraints | Q30439667 | ||
| Selection-Based Biodiversity at a Small Spatial Scale in a Low-Dispersing Insular Bird | Q30760651 | ||
| Physiological effects on demography: a long-term experimental study of testosterone's effects on fitness | Q34521345 | ||
| The evolutionary ecology of individual phenotypic plasticity in wild populations | Q34623676 | ||
| Quantitative evolutionary design | Q34745019 | ||
| Behavioral syndromes: an intergrative overiew | Q35941358 | ||
| Endocrinology of the stress response. | Q36041015 | ||
| Actions of glucocorticoids at a seasonal baseline as compared to stress-related levels in the regulation of periodic life processes | Q36453528 | ||
| Variation within and among species in gene expression: raw material for evolution | Q36454404 | ||
| Orchestration of avian reproductive effort: an integration of the ultimate and proximate bases for flexibility in clutch size, incubation behaviour, and yolk androgen deposition | Q36622268 | ||
| Sources of individual variation in plasma testosterone levels | Q36632986 | ||
| Integrating animal temperament within ecology and evolution | Q36793190 | ||
| Individual variation and the endocrine regulation of behaviour and physiology in birds: a cellular/molecular perspective | Q37019517 | ||
| A phylogenetically controlled test of hypotheses for behavioral insensitivity to testosterone in birds | Q38448093 | ||
| Corticosterone and foraging behavior in a pelagic seabird | Q40229548 | ||
| Hormones and the physiological architecture of life history evolution | Q40514596 | ||
| Variation within and between birds in corticosterone responses of great tits (Parus major). | Q40655112 | ||
| The matches, achieved by natural selection, between biological capacities and their natural loads | Q41125043 | ||
| The relationship of central and peripheral organ masses to aerobic performance variation in house sparrows | Q41684381 | ||
| Variation in continuous reaction norms: quantifying directions of biological interest | Q42040314 | ||
| Physiological and morphological correlates of among-individual variation in standard metabolic rate in the leopard frog Rana pipiens | Q42475556 | ||
| Plasma steroid-binding globulin mediation of differences in stress reactivity in alternative male phenotypes in tree lizards, Urosaurus ornatus | Q42497365 | ||
| Genetic characterization of stress responsiveness in Japanese quail. 2. Analyses of maternal effects, additive sex linkage effects, heterosis, and heritability by diallel crosses | Q44311004 | ||
| Comparative analysis of male androgen responsiveness to social environment in birds: the effects of mating system and paternal incubation | Q44466610 | ||
| Individual variation in plasma estradiol-17beta and androgen levels during egg formation in the European starling Sturnus vulgaris: implications for regulation of yolk steroids | Q44842646 | ||
| Mediation of a corticosterone-induced reproductive conflict | Q44950341 | ||
| The ecology of individuals: incidence and implications of individual specialization | Q45221147 | ||
| Heritability of plasma sex hormones and hormone binding globulin in adult male twins | Q45310736 | ||
| Behavioral syndromes: an ecological and evolutionary overview | Q46239775 | ||
| Is BMR repeatable in deer mice? Organ mass correlates and the effects of cold acclimation and natal altitude | Q46268792 | ||
| Experimental (antiestrogen-mediated) reduction in egg size negatively affects offspring growth and survival | Q46339736 | ||
| Interindividual differences in leg muscle mass and pyruvate kinase activity correlate with interindividual differences in jumping performance of Hyla multilineata. | Q46625135 | ||
| Does individual variation in stress responses and agonistic behavior reflect divergent stress coping strategies in juvenile rainbow trout? | Q46630932 | ||
| Monitoring reproductive aging in a 5-year prospective study: aggregate and individual changes in steroid hormones and menstrual cycle lengths with age. | Q46689656 | ||
| Growth selection in mice reveals conserved and redundant expression patterns of the insulin-like growth factor system | Q47931975 | ||
| Seasonal and individual variation in response to GnRH challenge in male dark-eyed juncos (Junco hyemalis). | Q48440761 | ||
| Plasma-binding globulins and acute stress response. | Q48447098 | ||
| Individual variation in cortisol responses to acute "on-back" restraint in an outbred hamster. | Q48699906 | ||
| Disparate release of prolactin and growth hormone from the tilapia pituitary in response to osmotic stimulation. | Q48720536 | ||
| Individual diurnal plasma profiles of thyroid hormones in rainbow trout (Oncorhynchus mykiss) in relation to cortisol, growth hormone, and growth rate. | Q50948721 | ||
| Fear of humans in Japanese quail selected for low or high adrenocortical response. | Q51132412 | ||
| Fasting-induced changes of immunological and stress indicators in breeding female eiders. | Q51500831 | ||
| Molecular and cellular studies in evolutionary physiology of natural vertebrate populations: influences of individual variation and genetic components on sampling and measurements. | Q51708372 | ||
| Individually variable energy management strategies in relation to energetic costs of egg production. | Q51718556 | ||
| Effects of testosterone and corticosterone on immunocompetence in the zebra finch. | Q51719525 | ||
| Antioxidant protection and plasma carotenoids of incubating great tits (Parus major L.) in relation to health state and breeding conditions. | Q51719866 | ||
| Multiple pathways of maternal effects in black-headed gull eggs: constraint and adaptive compensatory adjustment. | Q51799606 | ||
| Development of stress reactivity in white-crowned sparrow nestlings: total corticosterone response increases with age, while free corticosterone response remains low. | Q51999948 | ||
| Experimental manipulation of female reproduction reveals an intraspecific egg size-clutch size trade-off. | Q55399128 | ||
| Spatial ability is impaired and hippocampal mineralocorticoid receptor mRNA expression reduced in zebra finches (Taeniopygia guttata) selected for acute high corticosterone response to stress | Q57199237 | ||
| NATURAL SELECTION AND GENETIC VARIATION FOR REPRODUCTIVE REACTION NORMS IN A WILD BIRD POPULATION | Q57614395 | ||
| Mechanistic Analysis of Natural Selection and a Refinement of Lack's and Williams's Principles | Q59884550 | ||
| Heritability of corticosterone response and changes in life history traits during selection in the zebra finch | Q60430763 | ||
| Optimal immune responses: immunocompetence revisited | Q60430765 | ||
| Individual and sex specificity in the electric organ discharges of breeding mormyrid fish (Pollimyrus isidori) | Q68121816 | ||
| Individual differences among female rats in the timing of the preovulatory LH surge are predicted by lordosis reflex intensity | Q72567725 | ||
| Effect of divergent selection for total plasma phosphorus on plasma and yolk very low density lipoproteins and plasma concentrations of selected hormones in laying Japanese quail | Q73068762 | ||
| Follicular development and plasma yolk precursor dynamics through the laying cycle in the European starling (Sturnus vulgaris) | Q73825478 | ||
| Testosterone treatment is immunosuppressive in superb fairy-wrens, yet free-living males with high testosterone are more immunocompetent | Q73895740 | ||
| Cortisol levels are positively associated with pup-feeding rates in male meerkats | Q82825381 | ||
| Adaptation, Exaptation, and Constraint: A Hormonal Perspective | Q88190684 | ||
| P433 | issue | 1497 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 1687-1698 | |
| P577 | publication date | 2008-05-01 | |
| P1433 | published in | Philosophical Transactions of the Royal Society B | Q2153239 |
| P1476 | title | Individual variation in endocrine systems: moving beyond the 'tyranny of the Golden Mean'. | |
| P478 | volume | 363 |
| Q50963183 | A multidisciplinary study on social status and the relationship between inter-individual variation in hormone levels and agonistic behavior in a Neotropical cichlid fish. |
| Q64105446 | A negative correlation between behavioural and physiological performance under ocean acidification and warming |
| Q54987353 | A physiological perspective on fisheries-induced evolution. |
| Q90327267 | Across time and space: Hormonal variation across temporal and spatial scales in relation to nesting success |
| Q53586440 | Acute peaks of testosterone suppress paternal care: evidence from individual hormonal reaction norms. |
| Q42984705 | Acute stress induces a rapid increase of testosterone in a songbird: implications for plasma testosterone sampling |
| Q44935505 | Adrenocortical responses in zebra finches (Taeniopygia guttata): individual variation, repeatability, and relationship to phenotypic quality |
| Q43291918 | Aggression and related behavioral traits: the impact of winning and losing and the role of hormones |
| Q30487169 | Apparatus for collection of fecal samples from undisturbed spiny mice (Acomys cahirinus) living in a complex social group |
| Q44736874 | Are most samples of animals systematically biased? Consistent individual trait differences bias samples despite random sampling. |
| Q46520787 | Are yolk androgens adjusted to environmental conditions? A test in two seabirds that lay single-egg clutches. |
| Q52603707 | Avoiding the misuse of BLUP in behavioural ecology. |
| Q51409637 | Baseline and stress-induced glucocorticoid concentrations are not repeatable but covary within individual great tits (Parus major). |
| Q51175177 | Behavioural mediators of genetic life-history trade-offs: a test of the pace-of-life syndrome hypothesis in field crickets. |
| Q35754662 | Body Condition Indices Predict Reproductive Success but Not Survival in a Sedentary, Tropical Bird |
| Q33727854 | Child mortality, hypothalamic-pituitary-adrenal axis activity and cellular aging in mothers |
| Q30422540 | Competitive females are successful females; phenotype, mechanism and selection in a common songbird |
| Q46474843 | Conservation implications of a lack of relationship between baseline glucocorticoids and fitness in a wild passerine |
| Q31112768 | Context dependency of trait repeatability and its relevance for management and conservation of fish populations |
| Q48020666 | Corticosterone responses differ between lines of great tits (Parus major) selected for divergent personalities. |
| Q39989204 | Corticosterone responses in birds: individual variation and repeatability in Adelie penguins (Pygoscelisadeliae) and other species, and the use of power analysis to determine sample sizes. |
| Q48543037 | Corticosterone stress response shows long-term repeatability and links to personality in free-living Nazca boobies. |
| Q50439545 | Cortisol but not testosterone is repeatable and varies with reproductive effort in wild red deer stags. |
| Q38064515 | Determining the adaptive potential of maternal stress |
| Q47719624 | Distinct responses of baseline and stress-induced corticosterone levels to genetic and environmental factors |
| Q28600938 | Distribution and Abundance of Glucocorticoid and Mineralocorticoid Receptors throughout the Brain of the Great Tit (Parus major) |
| Q51165358 | Do smart birds stress less? An interspecific relationship between brain size and corticosterone levels. |
| Q43881695 | Do testosterone declines during the transition to marriage and fatherhood relate to men's sexual behavior? Evidence from the Philippines |
| Q38622508 | Does corticosterone regulate the onset of breeding in free-living birds?: The CORT-Flexibility Hypothesis and six potential mechanisms for priming corticosteroid function. |
| Q35082345 | Does feather corticosterone reflect individual quality or external stress in arctic-nesting migratory birds? |
| Q51134559 | Does stress response predict return rate in a migratory bird species? A study of American redstarts and their non-breeding habitat. |
| Q47755283 | Early-developmental stress, repeatability, and canalization in a suite of physiological and behavioral traits in female zebra finches |
| Q34765165 | Ecoimmunology for psychoneuroimmunologists: Considering context in neuroendocrine-immune-behavior interactions |
| Q47836266 | Effect of the early social environment on behavioural and genomic responses to a social challenge in a cooperatively breeding vertebrate. |
| Q90197269 | Emergence of consistent intra-individual locomotor patterns during zebrafish development |
| Q37343328 | Employing individual measures of baseline glucocorticoids as population-level conservation biomarkers: considering within-individual variation in a breeding passerine |
| Q38801104 | Endocrine Flexibility: Optimizing Phenotypes in a Dynamic World? |
| Q38431781 | Endocrine and neuroendocrine regulation of fathering behavior in birds |
| Q26774046 | Endocrine mechanisms, behavioral phenotypes and plasticity: known relationships and open questions |
| Q44540680 | Endocrine phenotype, reproductive success and survival in the great tit, Parus major |
| Q93380796 | Enzymatic antioxidants but not baseline glucocorticoids mediate the reproduction-survival trade-off in a wild bird |
| Q39264390 | Evidence for baseline glucocorticoids as mediators of reproductive investment in a wild bird |
| Q51145032 | Evolution of sex-specific pace-of-life syndromes: genetic architecture and physiological mechanisms. |
| Q46538890 | Evolutionary Endocrinology of Hormonal Rhythms: Juvenile Hormone Titer Circadian Polymorphism in Gryllus firmus |
| Q34355110 | Evolutionary and ecological approaches to the study of personality |
| Q51259012 | Experimental elevation of testosterone lowers fitness in female dark-eyed juncos. |
| Q34489111 | Experimental food restriction reveals individual differences in corticosterone reaction norms with no oxidative costs |
| Q57811389 | Experimental manipulation of a signal trait reveals complex phenotype-behaviour coordination |
| Q43117163 | Fecal cortisol metabolite levels in free-ranging North American red squirrels: Assay validation and the effects of reproductive condition |
| Q48121556 | Fuel, fasting, fear: routine metabolic rate and food deprivation exert synergistic effects on risk-taking in individual juvenile European sea bass |
| Q35596414 | Genetic variation in male sexual behaviour in a population of white-footed mice in relation to photoperiod |
| Q33550774 | Genotype-temperature interaction in the regulation of development, growth, and morphometrics in wild-type, and growth-hormone transgenic coho salmon. |
| Q91921033 | Glucocorticoids, male sexual signals, and mate choice by females: Implications for sexual selection |
| Q37168097 | Habits of the heart: life history and the developmental neuroendocrinology of emotion |
| Q58554675 | Habituation and individual variation in the endocrine stress response in the Trinidadian guppy (Poecilia reticulata) |
| Q33352846 | Hormonal organization and activation: evolutionary implications and questions |
| Q51609554 | Hormone levels predict individual differences in reproductive success in a passerine bird. |
| Q30439667 | Hormone-mediated suites as adaptations and evolutionary constraints |
| Q54997709 | HormoneBase, a population-level database of steroid hormone levels across vertebrates. |
| Q46167907 | Hormones and phenotypic plasticity in an ecological context: linking physiological mechanisms to evolutionary processes. |
| Q45035317 | Hormones as Mediators of Phenotypic and Genetic Integration: an Evolutionary Genetics Approach |
| Q37966424 | Hormones, life-history, and phenotypic variation: opportunities in evolutionary avian endocrinology |
| Q45377986 | Hormones, performance and fitness: Natural history and endocrine experiments on a lizard (Sceloporus undulatus). |
| Q41667452 | House finch responses to Mycoplasma gallisepticum infection do not vary with experimentally increased aggression. |
| Q28079737 | How can we estimate natural selection on endocrine traits? Lessons from evolutionary biology |
| Q48025491 | Individual variation and repeatability in urinary corticosterone metabolite responses to capture in the cane toad (Rhinella marina). |
| Q93076602 | Individual variation and the challenge hypothesis |
| Q47548670 | Individual variation in ACTH-induced cortisol levels in females of the livebearing fish at different gestational stages |
| Q51553924 | Individual variation in avian reproductive physiology does not reliably predict variation in laying date. |
| Q43291646 | Individual variation in baseline and stress-induced corticosterone and prolactin levels predicts parental effort by nesting mourning doves |
| Q30413171 | Individual variation in testosterone and parental care in a female songbird; the dark-eyed junco (Junco hyemalis) |
| Q46369909 | Individual versus pseudo-repeatability in behaviour: Lessons from translocation experiments in a wild insect. |
| Q47889371 | Initial reactivity and magnitude of the acute stress response associated with personality in wild great tits (Parus major). |
| Q51285901 | Introduction to the Symposium: Beyond the Mean: Biological Impacts of Changing Patterns of Temperature Variation. |
| Q36672009 | Introduction. Integration of ecology and endocrinology in avian reproduction: a new synthesis |
| Q86756807 | Is testis variation the key to understanding why males seem so different from one another? Commentary on "Examining sources of variation in HPG axis function among individuals and populations of the dark-eyed juncos". By Christine M. Bergeon Burns, |
| Q57235608 | Light loggers reveal weather-driven changes in the daily activity patterns of arboreal and semifossorial rodents |
| Q101632289 | Male mating success in a North American pitviper: influence of body size, testosterone, and spatial metrics |
| Q37153052 | Maternal effects in cooperative breeders: from hymenopterans to humans |
| Q38693268 | Measuring Selection on Physiology in the Wild and Manipulating Phenotypes (in Terrestrial Nonhuman Vertebrates). |
| Q54172406 | Micro-scale environmental variation amplifies physiological variation among individual mussels. |
| Q42633330 | Natural selection and glucocorticoid physiology |
| Q43527381 | Natural variation in steroid hormone profiles of male Timber Rattlesnakes, Crotalus horridus, in northwest Arkansas |
| Q39836312 | Natural variation in stress response is related to post-stress parental effort in male house sparrows |
| Q48790529 | Natural variation in the molecular stress network correlates with a behavioural syndrome. |
| Q51333784 | Neural sensitivity to sex steroids predicts individual differences in aggression: implications for behavioural evolution. |
| Q30538685 | Neural steroid sensitivity and aggression: comparing individuals of two songbird subspecies |
| Q33906980 | New insights into the hormonal and behavioural correlates of polymorphism in white-throated sparrows, Zonotrichia albicollis |
| Q34355064 | Personality and the emergence of the pace-of-life syndrome concept at the population level |
| Q33685171 | Phenology, seasonal timing and circannual rhythms: towards a unified framework |
| Q43814651 | Phenotypic integration and independence: Hormones, performance, and response to environmental change |
| Q46851928 | Physiological flexibility in an avian range expansion |
| Q59336190 | Physiological predictors of reproductive performance in the European Starling () |
| Q33421734 | Physiological stress mediates the honesty of social signals. |
| Q64241808 | Plasma mammalian leptin analogue predicts reproductive phenology, but not reproductive output in a capital-income breeding seaduck |
| Q47822043 | Pre-GnRH and GnRH-induced testosterone levels do not vary across behavioral contexts: A role for individual variation. |
| Q38424705 | Prolactin stress response does not predict brood desertion in a polyandrous shorebird |
| Q26824205 | Proximate perspectives on the evolution of female aggression: good for the gander, good for the goose? |
| Q48768617 | Receptors rather than signals change in expression in four physiological regulatory networks during evolutionary divergence in threespine stickleback. |
| Q38428932 | Repeatability of baseline and stress-induced corticosterone levels across early life stages in the Florida scrub-jay (Aphelocoma coerulescens). |
| Q51150450 | Repeatability of glucocorticoid hormones in vertebrates: a meta-analysis. |
| Q43110968 | Repeatable intra-individual variation in plasma testosterone concentration and its sex-specific link to aggression in a social lizard |
| Q30053374 | Reproductive rate, not dominance status, affects fecal glucocorticoid levels in breeding female meerkats |
| Q94538463 | Rising to the challenge? Inter-individual variation of the androgen response to social interactions in cichlid fish |
| Q41352047 | Risk-averse personalities have a systemically potentiated neuroendocrine stress axis: A multilevel experiment in Parus major. |
| Q57174551 | Sampling baseline androgens in free-living passerines: Methodological considerations and solutions |
| Q34899734 | Seasonal and individual variation in singing behavior correlates with α2-noradrenergic receptor density in brain regions implicated in song, sexual, and social behavior. |
| Q45814421 | Serum IGF-I in middle age covaries with reproductive life-history traits in British men and women |
| Q42693644 | Small increases in corticosterone before the breeding season increase parental investment but not fitness in a wild passerine bird |
| Q37367312 | Sources of variation in HPG axis reactivity and individually consistent elevation of sex steroids in a female songbird |
| Q91921027 | Stress hypothesis overload: 131 hypotheses exploring the role of stress in tradeoffs, transitions, and health |
| Q36329133 | Stress response to handling is short lived but may reflect personalities in a wild, Critically Endangered tortoise species. |
| Q39446253 | Stress responsiveness predicts individual variation in mate selectivity. |
| Q44171945 | Stress-induced rise in body temperature is repeatable in free-ranging Eastern chipmunks (Tamias striatus). |
| Q89499076 | Tales of testosterone: Advancing our understanding of environmental endocrinology through studies of neotropical birds |
| Q36069662 | Testosterone Mediates Seasonal Growth of the Song Control Nuclei in a Tropical Bird |
| Q93222252 | Testosterone administration in human social neuroendocrinology: Past, present, and future |
| Q38994933 | Testosterone and Haemosporidian Parasites Along a Tropical Elevational Gradient in Rufous-Collared Sparrows (Zonotrichia capensis). |
| Q36601784 | Testosterone and cortisol concentrations vary with reproductive status in wild female red deer |
| Q92129751 | Testosterone as a mediator of the tradeoff between cooperation and competition in the context of cooperative reproductive behaviors |
| Q39232696 | Testosterone production ability predicts breeding success and tracks breeding stage in male finches. |
| Q88882166 | Testosterone production and social environment vary with breeding stage in a competitive female songbird |
| Q57566237 | Testosterone production, sexually dimorphic morphology, and digit ratio in the dark-eyed junco |
| Q89858330 | Testosterone secretion varies in a sex- and stage-specific manner: Insights on the regulation of competitive traits from a sex-role reversed species |
| Q39981255 | The 'home advantage' is necessary for a full winner effect and changes in post-encounter testosterone. |
| Q46313722 | The Ecology of Exercise: Mechanisms Underlying Individual Variation in Behavior, Activity, and Performance: An Introduction to Symposium. |
| Q46754326 | The Power of Physiology in Changing Landscapes: Considerations for the Continued Integration of Conservation and Physiology |
| Q38906543 | The Tangled Evolutionary Legacies of Range Expansion and Hybridization |
| Q36961263 | The ecological and physiological bases of variation in the phenology of gonad growth in an urban and desert songbird |
| Q102063296 | The effects of food supply on reproductive hormones and timing of reproduction in an income-breeding seabird |
| Q51583248 | The glucocorticoid stress response is repeatable between years in a wild teleost fish. |
| Q28728288 | The role of motivation and reward neural systems in vocal communication in songbirds |
| Q38808827 | The role of the hypothalamus-pituitary-adrenal/interrenal axis in mediating predator-avoidance trade-offs. |
| Q47405227 | Uncoupling clutch size, prolactin, and luteinizing hormone using experimental egg removal |
| Q36050028 | Understanding the individual to implement the ecosystem approach to fisheries management |
| Q37922135 | Unfolding personalities: the importance of studying ontogeny |
| Q26752900 | Using an integrative approach to investigate the evolution of behaviour |
| Q40033313 | Using life-histories to predict and interpret variability in yolk hormones. |
| Q52838088 | Validation of a radioimmunoassay for measuring testosterone concentrations in plasma samples of the subterranean rodent Ctenomys talarum: outstandingly elevated levels in the wild and the effect of captivity. |
| Q46683811 | Variation among individuals in photoperiod responses: Effects of breeding schedule, photoperiod, and age-related photoperiodic experience in birds. |
| Q30432043 | Variation in levels of luteinizing hormone and reproductive photoresponsiveness in a population of white-footed mice (Peromyscus leucopus). |
| Q26778778 | When cooperation begets cooperation: the role of key individuals in galvanizing support |
| Q47999017 | Who is stressed? Comparing cortisol levels between individuals. |
| Q90685025 | Zebra finches bi-directionally selected for personality differ in repeatability of corticosterone and testosterone |
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