Higher dominance rank is associated with lower glucocorticoids in wild female baboons: A rank metric comparison.

Journal Article (Journal Article)

In vertebrates, glucocorticoid secretion occurs in response to energetic and psychosocial stressors that trigger the hypothalamic-pituitary-adrenal (HPA) axis. Measuring glucocorticoid concentrations can therefore shed light on the stressors associated with different social and environmental variables, including dominance rank. Using 14,172 fecal samples from 237 wild female baboons, we test the hypothesis that high-ranking females experience fewer psychosocial and/or energetic stressors than lower-ranking females. We predicted that high-ranking females would have lower fecal glucocorticoid (fGC) concentrations than low-ranking females. Because dominance rank can be measured in multiple ways, we employ an information theoretic approach to compare 5 different measures of rank as predictors of fGC concentrations: ordinal rank; proportional rank; Elo rating; and two approaches to categorical ranking (alpha vs non-alpha and high-middle-low). Our hypothesis was supported, but it was also too simplistic. We found that alpha females exhibited substantially lower fGCs than other females (typical reduction = 8.2%). If we used proportional rank instead of alpha versus non-alpha status in the model, we observed a weak effect of rank such that fGCs rose 4.2% from the highest- to lowest-ranking female in the hierarchy. Models using ordinal rank, Elo rating, or high-middle-low categories alone failed to explain variation in female fGCs. Our findings shed new light on the association between dominance rank and the stress response, the competitive landscape of female baboons as compared to males, and the assumptions inherent in a researcher's choice of rank metric.

Full Text

Duke Authors

Cited Authors

  • Levy, EJ; Gesquiere, LR; McLean, E; Franz, M; Warutere, JK; Sayialel, SN; Mututua, RS; Wango, TL; Oudu, VK; Altmann, J; Archie, EA; Alberts, SC

Published Date

  • September 2020

Published In

Volume / Issue

  • 125 /

Start / End Page

  • 104826 -

PubMed ID

  • 32758500

Pubmed Central ID

  • PMC7541639

Electronic International Standard Serial Number (EISSN)

  • 1095-6867

International Standard Serial Number (ISSN)

  • 0018-506X

Digital Object Identifier (DOI)

  • 10.1016/j.yhbeh.2020.104826


  • eng