Sexual segregation of forage patch use: Support for the social-factors and predation hypotheses.

Nearly all species of sexually dimorphic ungulates sexually segregate. Several hypotheses have been proposed to explain this phenomenon, including the social-factors hypothesis (SFH) and the predation hypothesis (PH). Interestingly, previous studies have accepted and rejected each hypothesis within and across species but few studies have simultaneously tested both hypotheses in the same population. In August 2011 and 2012 using 7680 photographs taken with camera traps in standardized forage patches, we tested two predictions of the SFH: 1) foraging efficiency of both sexes would decrease when foraging rate in mixed-sex groups relative to single-sex groups, and 2) activity patterns (i.e., the pattern of temporal use of forage patches on a diel scale) of the sexes would decrease in temporal overlap at the forage patch level (i.e., social segregation) compared to the overall temporal overlap of activity patterns of the population. Also, we tested two predictions of the +PH : 1) the relationship between feeding rates of each sex, and 2) temporal activity overlap would change with changing risk level of forage patches as a result of differing risk perception between sexes. In support of the SFH for temporal segregation, when in mixed-sex groups, mature males and all females decreased feeding rate 30% and 10%, respectively; further, the sexes had similar activity patterns overall (94-95% overlap), though temporal overlap was lower in individual forage patches (68-74% overlap). In multi-male mixed sex groups, at least one male exhibited aggressive posture toward females during all foraging bouts suggesting intersex aggression was the cause of the observed decrease in foraging rates. In support of the PH , the sexes adjusted feeding rate differently in response to changing risk level of a forage patch, encouraging spatial segregation; however, the PH was not supported for temporal segregation because temporal activity pattern overlap did not vary as a function of predation risk. Coupling our results with previous reports indicates that the SFH is supported for only temporal segregation of forage patch use, and the PH may only be supported for spatial segregation in forage patch use. Thus, both social factors and predation risk may interact to encourage sexual segregation.

White-tailed deer vigilance: the influence of social and environmental factors.

Vigilance behavior may directly affect fitness of prey animals, and understanding factors influencing vigilance may provide important insight into predator-prey interactions. We used 40,540 pictures taken withcamera traps in August 2011 and 2012to evaluate factors influencing individual vigilance behavior of white-tailed deer (Odocoileus virginianus) while foraging at baited sites. We used binary logistic regression to determine if individual vigilance was affected by age, sex, and group size. Additionally, we evaluated whether the time of the day,moon phase,and presence of other non-predatorwildlife species impacted individual vigilance. Juveniles were 11% less vigilant at baited sites than adults. Females were 46% more vigilant when fawns were present. Males and females spent more time feeding as group size increased, but with each addition of 1 individual to a group, males increased feeding time by nearly double that of females. Individual vigilance fluctuated with time of day andwith moon phase but generally was least during diurnal and moonlit nocturnal hours, indicating deer have the ability to adjust vigilance behavior to changing predation risk associated with varyinglight intensity.White-tailed deer increased individual vigilance when other non-predator wildlife were present. Our data indicate that differential effects of environmental and social constraints on vigilance behavior between sexes may encourage sexual segregation in white-tailed deer.