In animals, signaling behavior is often context-dependent, with variation in the probability of emitting certain signals dependent on fitness advantages. Senders may adjust signaling rate depending on receiver identity, presence of audiences, or noise masking the signal, all of which can affect the benefits and costs of signal production. In the cooperative breeding meerkat Suricata suricatta, group members emit soft contact calls, termed as “close calls”, while foraging in order to maintain group cohesion. Here, we investigated how the close calling rate during foraging was affected by the presence of pups, that produce continuous, noisy begging calls as they follow older group members. Adults decreased their overall close call rate substantially when pups were foraging with the group in comparison to periods when no pups were present. We suggest this decrease was likely due to a masking effect of the loud begging calls, which makes the close call function of maintaining group cohesion partly redundant as the centrally located begging calls can be used instead to maintain cohesion. There was some support that adults use close calls strategically to attract specific pups based on fitness advantages, that is, as the philopatric sex, females should call more than males and more to female pups than male pups. Dominant females called more than dominant males when a pup was in close proximity, while subordinates showed no sex-based differences. The sex of the nearest pup did not affect the calling rate of adults. The study shows that meerkats modify their close call production depending on benefits gained from calling and provides an example of the flexible use of one calling system in the presence of another, here contact calls versus begging calls, within the same species.
Solar power is a renewable energy source with great potential to help meet increasing global energy demands and reduce our reliance on fossil fuels. However, research is scarce on how solar facilities affect wildlife. With input from professionals in ecology, conservation, and energy, we conducted a research-prioritization process and identified key questions needed to better understand impacts of solar facilities on wildlife. We focused on animal behavior, which can be used to identify population responses before mortality or other fitness consequences are documented. Behavioral studies can also offer approaches to understand the mechanisms leading to negative interactions (e.g., collision, singeing, avoidance) and provide insight into mitigating effects. Here, we review how behavioral responses to solar facilities, Rachel Y. Chock, Barbara Clucas, and Elizabeth K. Peterson contributed equally to this study.
When the fitness costs and benefits of sons and daughters differ, offspring sex ratio manipulation could be an important reproductive tactic. We explored the effects of environment and maternal caring ability on offspring sex to test four adaptive sex ratio modification hypotheses: the extrinsic modification hypothesis (EMH), carrying capacity hypothesis (CCH), Trivers-Willard hypothesis (TWH), and cost-of-reproduction hypothesis (CRH). The EMH and CCH propose that environmental conditions shape offspring sex ratios, directly or in interaction with maternal condition. The TWH and CRH predict a positive relationship between maternal condition and production of the costlier sex. The TWH predicts that mothers with superior caring ability should produce more of the sex that can provide the greatest fitness returns from additional maternal allocation, and the CRH proposes that females with limited caring ability should reduce fitness costs by producing the cheaper sex. Repeated measures on 83 known-age eastern gray kangaroos, polygynous marsupials with strong sexual dimorphism, revealed that offspring sex ratio was independent of per capita forage, supporting neither the EMH nor CCH, but was dependent on maternal mass, consistent with the TWH and CCH. Our results, however, cannot clearly identify the ultimate cause of the relationship between maternal mass and greater production of sons. One of the three assumptions of the TWH could not be verified, and mothers of sons suffered only marginal additional fitness costs. Sex ratios in higher vertebrates are likely not solely explained by factors dependent on maternal control.
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