Capuchins (Sapajus apella) and squirrel monkeys (Saimiri sciureus) participated in 3 experiments in which they were presented with 2 objects, one appropriately oriented and the other inappropriately oriented to retrieve a food reward by pulling, replicating prior experiments with nonhuman primates described as evaluating "tool choice." Choice patterns were analyzed to assess whether monkeys learned that tools needed to be oriented with part of the tool on the far side of the reward to pull in the food. Both species learned to choose appropriately oriented tools after a similar number of sessions with a cane-shaped tool in the first task.
View Article and Find Full Text PDFAlthough play is seen in many species, its evolutionary function is still largely unknown. Several relevant, proposed hypotheses (such as the training for the unexpected, self-assessment, social skills, and dominance hierarchy hypotheses) make predictions about how animals should optimally choose their play partners based on their familiarity or other demographic variables. We used a social network approach to analyze focal sample data on brown capuchins (Cebus apella), hamadryas baboons (Papio hamadryas), and diademed sifaka (Propithecus diadema) to understand how these species choose their play partners with respect to demographic variables.
View Article and Find Full Text PDFLearning by watching others can provide valuable information with adaptive consequences, such as identifying the presence of a predator or locating a food source. The extent to which nonhuman animals can gain information by reading the cues of others is often tested by evaluating responses to human gestures, such as a point, and less often evaluated by examining responses to conspecific cues. We tested whether ten brown capuchin monkeys (Cebus [Sapajus] apella) were able to use cues from monkeys and a pointing cue from a human to obtain hidden rewards.
View Article and Find Full Text PDFPrevious research has suggested that several primate species may be capable of reasoning by exclusion based on the finding that they can locate a hidden object when given information about where the object is not. The present research replicated and extended the literature by testing 2 Old World monkey species, lion-tailed macaques (Macaca silenus) and a hamadryas baboon (Papio hamadryas), and 2 New World species, capuchin monkeys (Sapajus apella) and squirrel monkeys (Saimiri sciureus). The New World monkeys were tested on the traditional 2-way object choice task, and all 4 species were also tested on a more complex 3-way object choice task.
View Article and Find Full Text PDFMotor planning is a relatively complex cognitive skill in which an actor modifies a behavior to anticipate the future consequences of the action. Studying motor planning in nonhuman primates may provide a better understanding of the roots of human planning abilities. In this study we presented capuchin monkeys (Sapajus apella) with a horizontal dowel baited on either the left or right end.
View Article and Find Full Text PDFReduced space can lead to crowding in social animals. Crowding increases the risk of agonistic interactions that, in turn, may require additional physiological defensive coping mechanisms affecting health. To determine the stress induced from increased social density in a group of nineteen baboons living in an indoor/outdoor enclosure, saliva cortisol levels and rates of anxiety-related behavior were analyzed across two unique crowding episodes.
View Article and Find Full Text PDFCapuchin monkeys (Cebus sp.) are notable among New World monkeys for their widespread use of tools. Like chimpanzees, they use both hammer tools and insertion tools in the wild to acquire food that would be unobtainable otherwise.
View Article and Find Full Text PDFPictorial representations of three-dimensional objects are often used to investigate animal cognitive abilities; however, investigators rarely evaluate whether the animals conceptualize the two-dimensional image as the object it is intended to represent. We tested for picture recognition in lion-tailed macaques by presenting five monkeys with digitized images of familiar foods on a touch screen. Monkeys viewed images of two different foods and learned that they would receive a piece of the one they touched first.
View Article and Find Full Text PDFIn humans and several nonhuman animals, repetitive behavior is associated with deficits on executive function tasks involving response inhibition. We tested for this relationship in nonhuman primates by correlating rates of normative behavior to performance on a reversal-learning task in which animals were required to inhibit a previously learned rule. We focused on rates of self-directed behavior (scratch, autogroom, self touch and manipulation) because these responses are known indicators of arousal or anxiety in primates, however, we also examined rates of other categories of behavior (e.
View Article and Find Full Text PDFCirculating cortisol levels are often used to assess the biological stress response in captive primates. Some methods commonly used to collect blood samples may alter the stress response. As such, noninvasive means to analyze cortisol levels are increasingly being developed.
View Article and Find Full Text PDFJ Exp Psychol Anim Behav Process
January 2005
Using techniques established by E. M. Brannon and H.
View Article and Find Full Text PDFSome cercopithecine primates direct disproportionate amounts of grooming, huddling, and agonistic support toward maternal kin. Disproportionate amounts of aggression are also directed toward maternal kin, however, suggesting that mechanisms that restore relationships damaged by aggression, such as reconciliation, might be biased toward these preferred social partners. Studies investigating kinship effects and reconciliation are inconsistent, however, perhaps because of differences in the environmental conditions under which behavior was observed.
View Article and Find Full Text PDFData on social interactions with matrilineal kin were collected from two groups of rhesus monkeys for 6 years. All behavioral states, including time within one meter of another, involved kin more often than would be expected by chance. Significant associations were also found between kinship and the frequencies of various forms of agonistic as well as affiliative acts.
View Article and Find Full Text PDFSex differences in the behavior of 2.5- to 4.5-year-old rhesus monkeys, living in two social groups approximating natural compositions, were studied over a period of 3 years.
View Article and Find Full Text PDFTestosterone levels of 59 male rhesus monkeys were monitored over a period of 5 years. Longitudinal comparisons revealed consistent rises in mid-morning levels of circulating hormone in successive years from age 2.5 to 6.
View Article and Find Full Text PDFAdult male rhesus monkeys lose weight during the breeding season and regain it during the nonbreeding season. The annual pattern of maximum weight gain just prior to the onset of breeding resembles the seasonal "fattening" seen in squirrel monkeys, but the period of weight gain is less discrete. The magnitude of weight change is less in younger males, in that sexually immature males gain weight in both seasons, but significantly less during the breeding season.
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