delBarco-Trillo J.,Kalahari Research Trust |
delBarco-Trillo J.,Duke University |
delBarco-Trillo J.,Liverpool John Moores University |
Greene L.K.,Kalahari Research Trust |
And 16 more authors.
Hormones and Behavior | Year: 2016
In male vertebrates, androgens are inextricably linked to reproduction, social dominance, and aggression, often at the cost of paternal investment or prosociality. Testosterone is invoked to explain rank-related reproductive differences, but its role within a status class, particularly among subordinates, is underappreciated. Recent evidence, especially for monogamous and cooperatively breeding species, suggests broader androgenic mediation of adult social interaction. We explored the actions of androgens in subordinate, male members of a cooperatively breeding species, the meerkat (. Suricata suricatta). Although male meerkats show no rank-related testosterone differences, subordinate helpers rarely reproduce. We blocked androgen receptors, in the field, by treating subordinate males with the antiandrogen, flutamide. We monitored androgen concentrations (via baseline serum and time-sequential fecal sampling) and recorded behavior within their groups (via focal observation). Relative to controls, flutamide-treated animals initiated less and received more high-intensity aggression (biting, threatening, feeding competition), engaged in more prosocial behavior (social sniffing, grooming, huddling), and less frequently initiated play or assumed a 'dominant' role during play, revealing significant androgenic effects across a broad range of social behavior. By contrast, guarding or vigilance and measures of olfactory and vocal communication in subordinate males appeared unaffected by flutamide treatment. Thus, androgens in male meerkat helpers are aligned with the traditional trade-off between promoting reproductive and aggressive behavior at a cost to affiliation. Our findings, based on rare endocrine manipulation in wild mammals, show a more pervasive role for androgens in adult social behavior than is often recognized, with possible relevance for understanding tradeoffs in cooperative systems. © 2015 Elsevier Inc.
Smyth K.N.,Duke University |
Smyth K.N.,Kalahari Research Trust |
Drea C.M.,Duke University |
Drea C.M.,Kalahari Research Trust
Behavioral Ecology | Year: 2016
Within animal societies, demographic and social factors, as well as the different reproductive efforts of group members, may influence individual patterns of reproductive success and parasitism. In mammals, such relationships have been studied primarily in male-dominant species. To better understand these linkages in other social systems, we studied a female-dominant cooperative breeder, the meerkat (Suricata suricatta). This species is characterized by intense intrasexual competition and extreme reproductive skew in both sexes. Within adults, we examined heterogeneities in infection by 6 species of endoparasites in relation to host factors (e.g., weight, age, social status, sex, and group size). We explored potential trade-offs between reproduction and parasitism in dominant and subordinate animals of both sexes. Whereas weight and age were predictive of a few parasite taxa, social status or sex predicted parasite species richness and patterns of infection for the majority of parasites examined. Moreover, a significant interaction between sex and status for 2 nematode taxa revealed that dominant females were the most at risk of infection. Lastly, a positive relationship between group size and parasitism was evident in females only. In sum, compared with subordinates, dominant meerkats may experience increased exposure to directly transmitted parasites. Coupled with hormone-mediated immunosuppression, the increased susceptibility of dominant females may reflect energy allocation for preferentially maintaining dominance and breeding status over parasite defense. In species in which female intrasexual competition is intense, this trade-off between reproduction and health may be more pronounced in females than in males. © 2015 The Author 2015. Published by Oxford University Press on behalf of the International Society for Behavioral Ecology. All rights reserved. For permissions, please e-mail: firstname.lastname@example.org.
PubMed | Kalahari Research Trust and Duke University
Type: Journal Article | Journal: Biology letters | Year: 2017
The immunocompetence handicap hypothesis posits that androgens in males can be a double-edged sword, actively promoting reproductive success, while also negatively impacting health. Because there can be both substantial androgen concentrations in females and significant androgenic variation among them, particularly in species portraying female social dominance over males or intense female-female competition, androgens might also play a role in mediating female health and fitness. We examined this hypothesis in the meerkat (Suricata suricatta), a cooperatively breeding, social carnivoran characterized by aggressively mediated female social dominance and extreme rank-related reproductive skew. Dominant females also have greater androgen concentrations and harbour greater parasite loads than their subordinate counterparts, but the relationship between concurrent androgen concentrations and parasite burdens is unknown. We found that a females faecal androgen concentrations reliably predicted her concurrent state of endoparasitism irrespective of her social status: parasite species richness and infection by Spirurida nematodes, Oxynema suricattae, Pseudandrya suricattae and coccidia were greater with greater androgen concentrations. Based on gastrointestinal parasite burdens, females appear to experience the same trade-off in the costs and benefits of raised androgens as do the males of many species. This trade-off presumably represents a health cost of sexual selection operating in females.