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Little is known about white-tailed deer (Odocoileus virginianus) vigilance and how social interactions and rank, breeding chronology, and other factors affect their anti-predator behaviors. White-tailed deer typically are sexually segregated throughout most of the year  with males forming loose aggregations consisting of different age-classes outside of the breeding season [26,27]. Older and larger males tend to be dominant over immature males and adult females [28,29]. Among mature males, dominance is more correlated with body mass than age . In contrast, dominance among females is correlated with both increasing age  and body mass . Nevertheless, large, mature males hold the highest social rank followed by adult females, immature males, and juveniles.
There is an inverse relationship between foraging and vigilance whereby the cost of vigilance is a decrease in foraging. Therefore, in order to better understand foraging-vigilance tradeoffs, we investigated factors influencing foraging behavior, specifically the probability of feeding while at a concentrated food resource. We hypothesized that each sex-age class would show unique responses to reproductive (phase of breeding season), social (presence of different sex-age class, group size), predation risk (distance-to-forest), and abiotic (time-of-day) cues. We predicted males would exhibit stronger responses to socio-sexual factors than adult females and juveniles. We predicted adult females would be most sensitive to predation risk during the pre-breeding season when their offspring were more vulnerable to predation [13,16]. We predicted feeding would be greater during diurnal periods  but decrease as distance-to-forest increased because of greater perceived risk associated with open areas. We predicted that all sex-age classes would perceive less individual predation risk when foraging in larger groups [7,33] and consequently increase feeding. Finally, we predicted subordinate sex-age classes would decrease feeding when in the presence of a mature male as vigilance would likely be directed at avoiding agonistic interactions with the more dominant sex-age class [13,15].
Predictor variables include standardized distance-to-forest, time-of-day (day = 1, night = 0), season (pre-breeding, breeding, post-breeding), presence of a mature male, presence of an immature male, presence of an adult female, presence of a juvenile, group size, year, feeder type, and feeding site. Each model included year, feeder type, and feeding site. Feeding site was treated as a random effect.
We included the interactions between distance-to-forest and time-of-day as well as distance-to-forest and season because perceived predation risk may change according to the diel cycle or as physiological condition changes relative to the breeding season. For the mature and immature male models, we included an interaction between their presence and season as the frequency of agonistic interactions between males is influenced by the phase of the breeding season , and these interactions may influence resource acquisition rates. Additionally, for the adult female and juvenile models, we included interaction terms for their presence in the respective models and season as females may decrease feeding rates when juveniles are present . To control for potential differences in feeding rates influenced by year and feeder type, we included year and feeder type in each of our candidate models. We used Program R 3.1.2 for all statistical analyses .
Camera trapping effort was 375, 411, and 402 camera days for the pre-breeding, breeding, and post-breeding seasons, respectively. We collected 6,994 photographs containing images of 8,469 white-tailed deer for which we could assign a sex-age class. We recorded a total of 2,078 mature male, 2,479 immature male, 2,225 adult female, and 1,687 juvenile images. 041b061a72