... of adult growth. Life history Climate change Gill-oxygen limitation theory (GOLT) Growth modelling Energy allocation Australian Research Council http://dx.doi.org/10.13039/501100000923 FT180100154 Deakin University http://dx.doi.org/10.13039/501100001778...

...Alyssa M. Bonfoey; Jessica Chen; Zachary R. Stahlschmidt ABSTRACT Artificial light at night (ALAN) is increasingly prevalent worldwide, but life-history strategy may mitigate the costs of ALAN for animals. Yet, interactions among ALAN, life-history strategy and tolerance to climate-related...

... as a framework for future studies of animal form and function. First, studies of performance should consider the broader life-history context of the organism, and vice versa, as performance expression can require a large portion of acquired resources. Second, studies of life histories or mechanistic pathways...

...-flying mammals . Mech. Ageing Dev. 125 , 11 - 20 . 10.1016/j.mad.2003.09.003 Calder , W. A. ( 1984 ). Size, Function, and Life History . Courier Corporation . Clayton , D. H. , Koop , J. A. H. , Harbison , C. W. , Moyer , B. R. and Bush , S. E. ( 2010...

... of fast growth on telomerase activity, thus providing a new mechanism through which growth rates may affect telomere dynamics and potentially life-history trajectories. Body mass growth was not directly related to telomere length change in our initial SEM (standardized coefficient: −0.16, P =0.375...

...: Precocial birds incubated at low temperature take longer to develop cold tolerance, with possible costs for energy acquisition in early life. Body temperature Development Endothermy Heterothermy Life history Poultry Thermoregulation The demands of avian incubation often parallel, or even...

... life histories . Arch. Insect Biochem. Physiol.   35 , 359 - 373 . 10.1002/(SICI)1520-6327(1997)35:4<359::AID-ARCH2>3.0.CO;2-N Fernandez-Duque , E. ( 2009 ). Natal dispersal in monogamous owl monkeys (Aotus azarai) of the Argentinean Chaco . Behaviour   146 , 583 - 606 . 10.1163...

.../user-licence-1-1/ Highlighted Article: Related albatrosses have similar guard-stage foraging costs despite life history and foraging strategy differences; however, lighter forecasted wind in endemic albatross ranges may increase take-off costs and increase sit-and-wait strategies...

... that producing antibodies is either not very costly for green anoles or that all groups equally invest in antibodies regardless of energy limitation, as predicted by life-history theory ( Lochmiller and Deerenberg, 2000 ; Lee, 2006 ). Wound healing, by contrast, does appear costly, and high protein use may...

...Ben Dantzer; Freya van Kesteren; Sarah E. Westrick; Stan Boutin; Andrew G. McAdam; Jeffrey E. Lane; Robert Gillespie; Ariana Majer; Mark F. Haussmann; Pat Monaghan ABSTRACT Elevations in glucocorticoid (GC) levels in breeding females may induce adaptive shifts in offspring life histories. Offspring...

...Andy J. Turko; Justine E. Doherty; Irene Yin-Liao; Kelly Levesque; Perryn Kruth; Joseph M. Holden; Ryan L. Earley; Patricia A. Wright ABSTRACT Metabolic rate and life-history traits vary widely both among and within species, reflecting trade-offs in energy allocation, but the proximate and ultimate...

... leverage declines during growth in cottontail rabbits, likely promoting increased locomotor performance during the precarious juvenile period of life history. Muscle leverage Allometry Development Muscle force Life history Sub-adulthood can be a risky time of life for many animals...

.... This suggests that overwinter survival in diapause does not require larger energy reserves than direct development, likely because of metabolic suppression in diapause pupae. The results, nevertheless, demonstrate that physiological changes coincide with the divergence of life histories between the alternative...

... the mechanistic basis of fitness costs. Fourth, I propose the ‘redox signalling hypothesis’ of life history to complement the current ‘oxidative stress hypothesis’ of life history. The latter states that oxidative damage underlies trade-offs because it affects traits like growth, reproduction or cell senescence...

...-specific and varies with the life history traits of the individual. While the focus of this investigation was on the interaction between prior reproduction and oxidant exposure, we also evaluated the effects of reproduction, X-irradiation and reproduction+X-irradiation on the bioenergetic...

... and nutrient costs of glucocorticoid-accelerated development alter fitness trade-offs across life stages. Amphibian Life history Trade-off Glucocorticoids Corticosterone Stable isotopes Larval development is shaped by genetic and environmental interactions, and variation in conditions during...

... an ecological perspective, oxidative stress may serve as an important constraint to life-history traits, such as lifespan, reproduction and the immune system, and is gaining interest as a potential mechanism underlying life-history trade-offs. Of late, there has been much interest in understanding the role...

... that trained adults have enhanced growth, so juvenile growth is either insensitive to stimulation with exercise, or they are already growing at maximal rates. Our results add to a growing body of literature indicating that locomotor performance is an important part of life-history trade-offs that are sex...

...Jacob A. Jezovit; Joel D. Levine; Jonathan Schneider; Joel D. Levine; Daniel J. C. Kronauer; Michael H. Dickinson ABSTRACT Social behaviour emerges from the local environment but is constrained by the animal's life history and its evolutionary lineage. In this perspective, we consider the genus...

... temperature and CO 2 on life-history traits of two Drosophila species (Diptera: Drosophilidae) . Eur. J. Entomol.   93 , 451 - 459 . Brickner-Braun , I. ( 2014 ). The interrelationships between rodent respiration in a burrow environment and the physical ventilation of the burrow system...