Social learning of a communicative signal in captive chimpanzees

The acquisition of linguistic competency from more experienced social partners is a fundamental aspect of human language. However, there is little evidence that non-human primates learn to use their vocalizations from social partners. Captive chimpanzees (Pan troglodytes) produce idiosyncratic vocal signals that are used intentionally to capture the attention of a human experimenter. Interestingly, not all apes produce these sounds, and it is unclear what factors explain this difference. We tested the hypothesis that these attention-getting (AG) sounds are socially learned via transmission between mothers and their offspring. We assessed 158 chimpanzees to determine if they produced AG sounds. A significant association was found between mother and offspring sound production. This association was attributable to individuals who were raised by their biological mother-as opposed to those raised by humans in a nursery environment. These data support the hypothesis that social learning plays a role in the acquisition and use of communicative vocal signals in chimpanzees.     

Uncertain availability of a preferred food affects choice in a captive group of chimpanzees (Pan troglodytes)

Food-choice was investigated in a social group of 16 chimpanzees (Pan troglodytes) maintained in a large outdoor compound. Three feeding stations located along the periphery of the compound were considered analogous to food patches. Color-coded aluminum panels temporarily covered each feeding apparatus, with one color corresponding to nonpreferred food (commercial biscuits) available at two locations and other colors corresponding to the certain or uncertain availability of preferred food (oranges) available at one location. Only nine chimpanzees met the criterion for learning the color/food associations and thus only those animals were included in the analysis. There was a significant decrease in choosing the station associated with oranges when the probability of availability of oranges was reduced from 0.5 to 0.1 but not from 1.0 to 0.5. In addition, there was a significant increase in the frequency with which the subjects made no choice when the probability of availability of oranges was reduced from 1.0 to 0.1. The data indicate that the uncertain availability of preferred food in a choice situation affects choice behavior in a social group of chimpanzees studied under controlled conditions.     

Social factors influencing choice of food source in a captive group of chimpanzees (Pan troglodytes)

The influence of social factors, including social relationship, kinship, estrous cycle stage and hierarchical rank, on choice of a food source was studied in a group of 16 chimpanzees (Pan troglodytes) maintained in a large, outdoor compound. The subjects chose among three feeding stations that were spatially separated and located along the periphery of the compound. One feeding station was associated with a preferred food (orange), and two stations contained a less-preferred food (commercial chow or biscuit). A significant positive correlation was found between (a) the frequency with which one animal groomed another and the frequency with which they chose the same station during a given trial and (b) the percent of time that subjects were in close proximity and the frequency with which they chose the same station during a given trial, and this result was mediated by kinship. There was a significant difference in same-station choice by the adult male and by a maximally tumescent female compared to the choice when that female was detumescent. Finally, there was no significant correlation between social rank and the percent of trials during which the station associated with the more highly preferred food type was chosen. This study provided quantitative data supporting postulations that factors such as social relationship, kinship, and estrous cycle stage affect the composition of groupings of chimpanzees at feeding stations, and the results are consistent with field observations.     

Hand preferences of captive chimpanzees (Pan troglodytes) in simple reaching for food

We examined chimpanzee hand preference in simple reaching for food, with special reference to manipulative patterns and the developmental shift. We observed 80 captive chimpanzees, ranging from 1 to 25 years old. We also studied the manipulative patterns (grip- types) of 70 individuals as they reached for raisins scattered randomly on the floor. We employed LQ score as a measure of hand preference and designated the subjects right- handers (or left- handers) if they used their right hands (left hands) above chance level. Although the numbers of right- handers and left- handers are almost equal, the distribution of the strength is not symmetrical in both groups. Strong preference was exhibited by more left- handers than right- handers. Subjects > 9 years old exhibited greater hand preference, whereas subjects < 9 years old were ambidextrous. We classified manipulative patterns for reaching into five basic grip- types and analyzed them vis- à- vis age. There is no significant correlation between preferred hand and manipulative patterns. However, adult subjects tended to use an index- and - middle- finger grip with the left hand and to use imprecise grips with the right hand more often than other patterns regardless which hand they preferred. These data demonstrate a developmental shift in hand preference and manipulative patterns and also reveal functional asymmetries between the right and the left hand in Pan troglodytes.     

Evaluation of introduction procedures in captive chimpanzees

Chimpanzee introductions can be stressful and even dangerous for the individuals involved, and different facilities use different approaches to group formation. However, little empirical evidence has been available to evaluate the different factors related to successful or unsuccessful chimpanzee introductions. This study evaluated a variety of factors, such as age, sex, previous experience, and the behavior displayed during the initial introduction period, to determine any influence on the outcome of the introduction in 165 dyadic introduction events. The direct introduction of one chimpanzee to a group or to another individual resulted in an overall success rate of 86.7%. The first few social interactions were characterized by more aggressive and submissive behavior than afffiliative behavior, but this trend was quickly reversed. Unsuccessful outcomes were more common if wounding occurred, if either individual was male, and if the newcomer had high levels of submissive behavior. Among male chimpanzees, the behaviors during the first 10 min of the introductions were characterized by more submissive behavior of the newcomer and more aggressive behavior of the introduction partner. The frequency of aggression by the introduction partner was higher when the newcomer was introduced to one chimpanzee at a time rather than to the group as a whole. This information may have important consequences for how we view chimpanzee group formation, and factors such as previous experience and aggression may be less important than the method of introduction and the level of submissive behavior. Zoo Biol 16:335–342, 1997. © 1997 Wiley-Liss, Inc.     

Sleeping behavior and associations in a group of captive chimpanzees.

The present study investigated the sleeping behavior and preferences of a group of six adolescent chimpanzees at the Delta Regional Primate Research Center in Louisiana, USA. The study sought to relate sleeping partner preferences to other aspects of social relationships. Comparative observations between those chimpanzee behaviors seen in the wild and in this group are noted.     

Hand preferences of captive chimpanzees (Pan troglodytes) in simple reaching for food

We examined chimpanzee hand preference in simple reaching for food, with special reference to manipulative patterns and the developmental shift. We observed 80 captive chimpanzees, ranging from 1 to 25 years old. We also studied the manipulative patterns (grip- types) of 70 individuals as they reached for raisins scattered randomly on the floor. We employed LQ score as a measure of hand preference and designated the subjects right- handers (or left- handers) if they used their right hands (left hands) above chance level. Although the numbers of right- handers and left- handers are almost equal, the distribution of the strength is not symmetrical in both groups. Strong preference was exhibited by more left- handers than right- handers. Subjects > 9 years old exhibited greater hand preference, whereas subjects < 9 years old were ambidextrous. We classified manipulative patterns for reaching into five basic grip- types and analyzed them vis- à- vis age. There is no significant correlation between preferred hand and manipulative patterns. However, adult subjects tended to use an index- and - middle- finger grip with the left hand and to use imprecise grips with the right hand more often than other patterns regardless which hand they preferred. These data demonstrate a developmental shift in hand preference and manipulative patterns and also reveal functional asymmetries between the right and the left hand in Pan troglodytes.     

The acquisition of stone-tool use in captive chimpanzees

In order to investigate the acquisition of stone-tool use to crack nuts, experiments were conducted with five captive chimpanzees, employing combinations of trial-and-error, and three types of observation learning of varied difficulty. Two adults and one sub-adult succeeded in acquiring this behavior in the tests where tool use was demonstrated by the experimenter, or by a successful chimpanzee. Analysis of their behavior patterns showed the adults' and sub-adult's process to success to be divided into three stages; these can be characterized as trial-and-error, understanding of the method, and learning the technique, respectively. A factor for distinguishing success from failure is whether or not a subject observes demonstrations with interest in the behavior itself. This interest, in turn, depends on the intensity of the desire for nuts. When released, the successful chimpanzees practiced the same behavior in a group of chimpanzees, and the behavior newly diffused to an infant. Unlike the adults, the infant did not go through the staged process but reached the solution through goal-directed trial-and-error.     

The brutal elimination of a rival among captive male chimpanzees

The relationships among three adult male chimpanzees (Pan troglodytes) were observed over a period of 6 years. The males were members of a large, mixed colony of chimpanzees at Arnhem Zoo (Netherlands). In spite of several power takeovers and coalition changes among the males, aggression was restrained during most of the period. This article analyzes a dramatic exception, which occurred after months of instability in the coalition network. At night, the alpha male was attacked and fatally injured in the sleeping quarters. The incident is discussed against the background of the complex balance of power among the males, especially the discrepancy between coalitions serving hierarchical status and coalitions serving sexual competition. Quantitative data support most of the hypotheses.     

The effects of social status on food-associated calling behaviour in captive cotton-top tamarins

We examined the effects of social environment on food-asociated calling of cotton-top tamarins, Saguinus oedipus, in two experiments. In experiment 1, we compared the food-associated calling behaviour of six juvenile tamarins living in their natal groups with their calling behaviour 9 months after being removed from family groups and paired. In experiment 2, we studied food-associated calling behaviour of nine cotton-top tamarins immediately before and after removal from their natal groups and pairing. The tamarins underwent three separate developmental processes in their calling behaviour. Animals removed from their natal groups showed an immediate reduction in vocalizations other than food-associated calls (C and D chirps). The development of precise adult forms of C and D chirps was more gradual and was a function of time since removal from their natal group rather than time since pairing. Finally, the postremoval tamarins persisted in applying C chirps to nonfood objects and showed no correlation between C-chirp rate and food preference, which is typical of immature tamarins. We conclude that social status plays an important role in the development of adult forms and usage of food-associated calls. Copyright 1999 The Association for the Study of Animal Behaviour.     

Social grooming and play behavior of a captive group of chimpanzees

Aspects of the social grooming and play behavior of a group of six adolescent and young adult chimpanzees are contrasted and compared. Eleven months’ data indicate that older chimpanzees groomed more and played less than younger individuals. This transition period occurred earlier for females than males. Grooming behavior appeared to vary with reproductive state. A positive correlation was found between the estrous condition of cycling females and the amount of grooming that they received from the males. A mother of a young infant received particularly high levels of grooming from the other group members. Less variation among individuals was found for frequencies of play as compared to grooming. Play dropped following the death of one individual and was entirely inhibited for three weeks following the group’s transfer to a new environment and the reintroduction of a former group member. Comparison to a free-ranging population indicates important differences in both frequencies and general patterns of play and grooming.     

Hand preference in a captive island group of chimpanzees (Pan troglodytes)

Morphological cerebral asymmetries in chimpanzee brains, similar to those found in humans, in whom they are associated with speech and handedness, suggest the possibility of functional lateralization in the chimpanzee. This possibility was investigated by examining hand preferences in an island group of five chimpanzees on a series of unimanual and bimanual tasks that are diagnostic of human hand and cerebral dominance. Each subject was tested in a double compartment cage on three unimanual nonsequential, three unimanual sequential, and three bimanual coordination tasks. One of the three unimanual sequential tasks was a bar-press task that is analogous to the commonly used human finger-tapping task. For the unimanual tasks, exclusive of the bar-press, the chimpanzees showed a highly individualistic pattern of hand preference that did not change as a function of task complexity. On the bar-press task, four of five subjects produced higher rates with one hand compared to the other; however, relative hand performance on this task was unrelated to hand preference on the other unimanual tasks. For the group of subjects, performance rates did not differ between the left and right hands; however, a practice effect was observed for the right hand in all subjects. The bimanual tasks also revealed a complex pattern of individual handedness, with no trends apparent for the group as a whole. Consistent with previous findings, the results from these tests on this group of five chimpanzees suggest that cerebral morphological asymmetries in the chimpanzee are not associated with motor dominance as reflected in handedness.     

Epidemiological study of zoonoses derived from humans in captive chimpanzees

Emerging infectious diseases (EIDs) in wildlife are major threats both to human health and to biodiversity conservation. An estimated 71.8 % of zoonotic EID events are caused by pathogens in wildlife and the incidence of such diseases is increasing significantly in humans. In addition, human diseases are starting to infect wildlife, especially non-human primates. The chimpanzee is an endangered species that is threatened by human activity such as deforestation, poaching, and human disease transmission. Recently, several respiratory disease outbreaks that are suspected of having been transmitted by humans have been reported in wild chimpanzees. Therefore, we need to study zoonotic pathogens that can threaten captive chimpanzees in primate research institutes. Serological surveillance is one of several methods used to reveal infection history. We examined serum from 14 captive chimpanzees in Japanese primate research institutes for antibodies against 62 human pathogens and 1 chimpanzee-borne infectious disease. Antibodies tested positive against 29 pathogens at high or low prevalence in the chimpanzees. These results suggest that the proportions of human-borne infections may reflect the chimpanzee’s history, management system in the institute, or regional epidemics. Furthermore, captive chimpanzees are highly susceptible to human pathogens, and their induced antibodies reveal not only their history of infection, but also the possibility of protection against human pathogens.     

Geographic variation in the calls of wild chimpanzees: A reassessment

Male chimpanzees produce a species‐typical call, the pant hoot, to communicate to conspecifics over long‐distances. Calls given by males from the well‐known Gombe and Mahale populations typically consist of four different phases: an introduction, build‐up, climax, and let‐down. Recent observations suggest that chimpanzees living in the Kibale National Park, Uganda, consistently give calls that lack a build‐up and are thus qualitatively distinguishable acoustically from those made by other East African conspecifics. We analyzed additional recordings from Mahale and Kibale to re‐examine geographic variation in chimpanzee calls. Results indicate that males from both sites produce pant hoots containing all four parts of the call. Calls made by chimpanzees from the two populations, however, differ in quantitative acoustic measures. Specifically, males at Kibale initiate their calls with significantly longer elements and build‐up over briefer periods at slower rates than individuals from Mahale. Kibale males also deliver acoustically less variable calls than chimpanzees at Mahale. Although climax elements do not differ between populations in any single acoustic feature, discriminant function analysis reveals that acoustic variables can be used in combination to assign calls to the correct population at rates higher than that expected by chance. Ecological factors related to differences in habitat acoustics, the sound environment of the local biota, and body size are likely to account for these observed macrogeographic variations in chimpanzee calls. Am. J. Primatol. 47:133–151, 1999. © 1999 Wiley‐Liss, Inc.     

Acoustic variation of pant hoot calls by male chimpanzees: a playback experiment

Pant hoots, a type of long-distance calls of chimpanzees (Pan troglodytes), were played back to two male chimpanzees in a group of seven captive individuals to determine if chimpanzees would modify those vocalizations in response to strange males. Subjects emitted pant hoots with higher rates of delivery, shorter duration of buildup, and lower minimum fundamental frequency of climax when they were presented with pant hoots of strangers than when they produced the calls spontaneously. Considering the direction of acoustical change, we concluded that the rate of delivery, duration of buildup, and minimum frequency of climax might be associated with the underlying emotional states of the callers rather than call matching. Individual difference between two subject males was significant in minimum frequency and duration of climax and in average frequency of call, which appears to reflect differences of the caller's age and social status. These results suggest that different acoustic variables relate to within- and interindividual differences of these vocalizations. Received: March 7, 2000 / Accepted: May 8, 2000     

The behavior of a group of captive pygmy chimpanzees (Pan paniscus)

A group of captive pygmy chimpanzees (Pan paniscus) was studied in the San Diego Zoological Gardens. The behavior patterns that these animals exhibit are described. Each of these behavior patterns is compared to those described for wild and captive common chimpanzees (P. troglodytes). Differences in behavior between these two species are attributed to specialization of the pygmy chimpanzee to a rain forest habitat and to a monogamous social system.