| Literature DB >> 34133269 |
Cédric Girard-Buttoz1,2, Patrick J Tkaczynski1,2, Liran Samuni2,3,4, Pawel Fedurek5, Cristina Gomes6, Therese Löhrich7,8, Virgile Manin1,2, Anna Preis3, Prince F Valé2,3,9,10, Tobias Deschner11, Roman M Wittig1,2, Catherine Crockford1,2,12.
Abstract
The biological embedding model (BEM) suggests that fitness costs of maternal loss arise when early-life experience embeds long-term alterations to hypothalamic-pituitary-adrenal (HPA) axis activity. Alternatively, the adaptive calibration model (ACM) regards physiological changes during ontogeny as short-term adaptations. Both models have been tested in humans but rarely in wild, long-lived animals. We assessed whether, as in humans, maternal loss had short- and long-term impacts on orphan wild chimpanzee urinary cortisol levels and diurnal urinary cortisol slopes, both indicative of HPA axis functioning. Immature chimpanzees recently orphaned and/or orphaned early in life had diurnal cortisol slopes reflecting heightened activation of the HPA axis. However, these effects appeared short-term, with no consistent differences between orphan and non-orphan cortisol profiles in mature males, suggesting stronger support for the ACM than the BEM in wild chimpanzees. Compensatory mechanisms, such as adoption, may buffer against certain physiological effects of maternal loss in this species.Entities:
Keywords: biological embedding model; chimpanzees; developmental biology; early life adversity; evolutionary biology; long-lived mammals; orphan; stress physiology
Year: 2021 PMID: 34133269 DOI: 10.7554/eLife.64134
Source DB: PubMed Journal: Elife ISSN: 2050-084X Impact factor: 8.140