EQUIPPED FOR LIFE: THE ADAPTIVE ROLE OF THE STRESS AXIS IN MALE MAMMALS

By R. Boonstra. 2005

191 citations recorded by the source corpus.

Subfields: Behavioral Neuroscience, Ecology, Evolution, Behavior and Systematics, Social Psychology

View Paper: https://www.semanticscholar.org/paper/1d2757cfcc6fc3ef5a6038e5f52e8da3564d520f

How researchers see this paper

The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.

In Behavioral Neuroscience

1. D. Reeder
2. K. M. Kramer
3. R. Boonstra
4. M. Sheriff
5. J. Wingfield
6. P. Monaghan
7. D. Nussey
8. R. Ricklefs

In Ecology, Evolution, Behavior and Systematics

1. J. Wingfield
2. D. Reeder
3. K. M. Kramer
4. W. Goymann
5. M. Sheriff
6. R. Boonstra
7. D. Nussey
8. Denis Réale

In Social Psychology

1. D. Reeder
2. K. M. Kramer
3. J. Wingfield
4. Brendan Delehanty
5. M. Sheriff
6. D. Nussey
7. P. Monaghan
8. R. Ricklefs

Citations in the corpus

• The evolutionary ecology of senescence (2008, methodology): “The hormesis hypothesis is similar to Wingfield et al. ’s ideas about the effects of stress realised through the hypothalamic‐ pituitary‐adrenal (HPA) axis, mediated by glucocorticoid secretions ( Boonstra 1994, 2005; Wingfield et al. 1998).”
• Personality differences are related to long-term stress reactivity in a population of wild eastern chipmunks, Tamias striatus (2012, background): “…differences inboldness, exploration and aggressiveness are related to differences in the autonomic nervous system and the hypothalamicepituitaryeadrenal axis, regulating how individuals react to environmental perturbations or stress (Koolhaas et al. 1999; Boonstra 2005; Reeder & Kramer 2005).”
• Maternal adversity and ecological stressors in natural populations: the role of stress axis programming in individuals, with implications for populations and communities (2013, background): “Functional Ecology © 2012 British Ecological Society hypthothalamus-pituitary-adrenal (‘stress’) axis across vertebrate taxa underscores the biological importance of optimal GC management (Boonstra 2005; Wingfield 2005; Breuner, Patterson & Hahn 2008).”
• Hair cortisol concentration as a noninvasive measure of long-term stress in free-ranging grizzly bears (Ursus arctos): considerations with implications for other wildlife (2010, background): “Differences in basal levels of circulating glucocorticoids along with the strength and activity of the stress response have been attributed to variation in sex and age in a variety of mammals (Boonstra 2005; Reeder and Kramer 2005).”
• STRESS IN FREE-RANGING MAMMALS: INTEGRATING PHYSIOLOGY, ECOLOGY, AND NATURAL HISTORY (2005, methodology): “…the necessity of collecting samples within 3 min but the results represent total Downloaded from https://academic.oup.com/jmammal/article-abstract/86/2/225/890330 by guest on 29 July 2018 glucocorticoid output over an unknown period of time rather than acute or immediate values (Boonstra 2005).”
• The ecology of stress: effects of the social environment (2013, background): “The HPA axis integrates environmental information and the downstream release of glucocorticoids can potentiate an adaptive behavioural response (Monclús et al. 2005; Schulkin, Morgan & Rosen 2005) or alteration in life-history strategy (Wingfield et al. 1998; Boonstra 2005).”
• Evaluating stress in natural populations of vertebrates: total CORT is not good enough (2013, background): “In the case of the latter, animals may have evolved to repress or accentuate certain portions of the stress axis (Wingfield & Sapolsky 2003; Boonstra 2005).”
• THE CONCEPT OF ALLOSTASIS: COPING WITH A CAPRICIOUS ENVIRONMENT (2005, background): “Examples of type 2 allostatic overload in natural populations of vertebrates are few, but it is of interest to note that the effect of predator density on populations of snowshoe hares (Lepus americanus) may be an example (Boonstra 2005; Boonstra and Singleton 1993).”