Breeding-Related Changes in Social Interactions Among Female Vulturine Guineafowl

IF 2.3 2区 生物学 Q2 ECOLOGY Ecology and Evolution Pub Date : 2025-01-31 DOI:10.1002/ece3.70943
Tobit Dehnen, Brendah Nyaguthii, Wismer Cherono, Neeltje J. Boogert, Damien R. Farine
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Abstract

Agonistic and affiliative interactions with group members dictate individual access to resources, and investment in competing for resources is often traded off with other needs. For example, reproductive investment can reduce body condition and, thereby, an individual's ability to win future agonistic interactions. However, group members may also alter their behaviour towards reproductive individuals, such as becoming more or less aggressive. Here, we investigated the social consequences of reproduction in female vulturine guineafowl Acryllium vulturinum, a plural breeder in which females disperse and are subordinate to males. We found opposing patterns for within- and between-sex dominance interactions experienced by females from before to after breeding. Specifically, breeding females became far less likely to win dominance interactions with non-breeding females after breeding than before breeding, but received considerably fewer male aggressions than non-breeding females after breeding. Despite a limited sample size, our study reveals that reproduction can have nuanced trade-offs with dominance and suggests that the study of dominance may benefit from explicitly considering variation in interaction rates as an additional factor affecting individuals.

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雌性兀鹰珍珠鸡社会交往的繁殖相关变化。
与群体成员的竞争和从属互动决定了个人对资源的访问,而对资源竞争的投资往往与其他需求相交换。例如,生殖投资可以降低身体状况,从而降低个体赢得未来竞争相互作用的能力。然而,群体成员也可能改变他们对繁殖个体的行为,比如变得更有攻击性或更少攻击性。本文研究了秃鹰(acrylium vulturinum)雌性繁殖的社会后果。秃鹰是一种雌性分散并服从于雄性的多元繁殖动物。我们发现雌性在繁殖前和繁殖后所经历的性别内和性别间优势互动是相反的模式。具体来说,繁殖雌性在繁殖后与非繁殖雌性的优势互动比繁殖前要少得多,但在繁殖后受到的雄性攻击却比非繁殖雌性少得多。尽管样本量有限,但我们的研究表明,繁殖可以与优势进行微妙的权衡,并建议将相互作用率的变化作为影响个体的另一个因素明确考虑,对优势的研究可能有益。
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来源期刊
CiteScore
4.40
自引率
3.80%
发文量
1027
审稿时长
3-6 weeks
期刊介绍: Ecology and Evolution is the peer reviewed journal for rapid dissemination of research in all areas of ecology, evolution and conservation science. The journal gives priority to quality research reports, theoretical or empirical, that develop our understanding of organisms and their diversity, interactions between them, and the natural environment. Ecology and Evolution gives prompt and equal consideration to papers reporting theoretical, experimental, applied and descriptive work in terrestrial and aquatic environments. The journal will consider submissions across taxa in areas including but not limited to micro and macro ecological and evolutionary processes, characteristics of and interactions between individuals, populations, communities and the environment, physiological responses to environmental change, population genetics and phylogenetics, relatedness and kin selection, life histories, systematics and taxonomy, conservation genetics, extinction, speciation, adaption, behaviour, biodiversity, species abundance, macroecology, population and ecosystem dynamics, and conservation policy.
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