Nesting strategy shapes territorial aggression but not testosterone: A comparative approach in female and male birds.

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2021-07

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Abstract

Our understanding of the proximate and ultimate mechanisms shaping competitive reproductive phenotypes primarily stems from research on male-male competition for mates, even though competition is widespread in both sexes. We evaluate the hypothesis that the restricted nature of a resource required for reproduction, i.e. nest site, is a key variable driving territorial competition and testosterone secretion in female and male birds. Obligate secondary cavity-nesting has evolved repeatedly across avian lineages, providing a useful comparative context to explore how competition over limited nest cavities shapes aggression and its underlying mechanisms across species. Although evidence from one or another cavity-nesting species suggests that territorial aggression is adaptive in both females and males, this has not yet been tested in a comparative framework. We predicted that cavity-nesting generates more robust territorial aggression, in comparison to close relatives with less restrictive nesting strategies. Our focal species were two obligate secondary cavity-nesting species and two related species with more flexible nesting strategies in the same avian family: tree swallow (Tachycineta bicolor) vs. barn swallow (Hirundo rustica); Eastern bluebird (Sialia sialis) vs. American robin (Turdus migratorius). We assayed conspecific aggression using simulated territorial intrusion and found that cavity-nesting species displayed greater territorial aggression than their close relatives. This pattern held for both females and males. Because territorial aggression is often associated with elevated testosterone, we also hypothesized that cavity-nesting species would exhibit higher testosterone levels in circulation. However, cavity-nesting species did not have higher testosterone in circulation for either sex, despite some correlative evidence that testosterone is associated with higher rates of physical attack in female tree swallows. Our focus on a context that is relevant to both sexes - competition over essential breeding resources - provides a useful framework for co-consideration of proximate and ultimate drivers of reproductive competition in females and males.

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10.1016/j.yhbeh.2021.104995

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Lipshutz, Sara E, and Kimberly A Rosvall (2021). Nesting strategy shapes territorial aggression but not testosterone: A comparative approach in female and male birds. Hormones and behavior, 133. p. 104995. 10.1016/j.yhbeh.2021.104995 Retrieved from https://hdl.handle.net/10161/28955.

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Lipshutz

Sara E Lipshutz

Assistant Professor of Biology

Our research focuses on the evolution of behavior across weird and wonderfully diverse species of birds. This work bridges “muddy boots” experimental fieldwork with a variety of molecular and computational approaches in genetics, genomics, neuroscience, and endocrinology. We have several research foci:  

 

1. Female perspectives in biology. Cultural biases shape our predictions for how and why animals behave the way they do, and female animals have historically been neglected in biological research. We study the evolution of female competition across diverse avian species, ranging from social polyandry to monogamy in shorebirds and songbirds. Critically, hypotheses derived from studying males (i.e. testosterone focus) do not explain interspecific variation in female aggression. We use population genomic and transcriptomic data to evaluate the proximate causes and ultimate consequences of female competition.  

 

2. Global change biology. In the age of the Anthropocene, animals are facing evolutionary unprecedented environmental changes. Sensory pollutants like anthropogenic noise and artificial light at night can alter animal physiology, behavior, and ecology on a rapid timescale. Behavior flexibility and adaptation may lead the way in helping animals respond to novel challenges. We investigate why some individuals and species may be better prepared to face global change.  


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