Imaginary Play in chimpanzees (Pan troglodytes)

Imaginary Play was studied in a group of five signing chimpanzees and it was found that chimpanzees engage in imaginary play similar to that found in human children. Fifteen hours of remote videotapes were analyzed for instances of imaginary play. Behaviors were defined as imaginary play by meeting a predetermined criteria which allowed them to be classified into one of six different categories of imaginary play. Six instances of imaginary play were found and these were classified into the two categories of Animation and Substitution. Observations of imaginary play in other research with chimpanzees were discussed.     

Comparing infant and juvenile behavior in bonobos (Pan paniscus) and chimpanzees (Pan troglodytes): a preliminary study

The dichotomy between the two Pan species, the bonobo (Pan paniscus) and chimpanzee (Pan troglodytes) has been strongly emphasized until very recently. Given that most studies were primarily based on adult individuals, we shifted the “continuity versus discontinuity” discussion to the infant and juvenile stage. Our aim was to test quantitatively, some conflicting statements made in literature considering species differences between immature bonobos and chimpanzees. On one hand it is suggested that infant bonobos show retardation in motor and social development when compared with chimpanzees. Additionally it is expected that the weaning process is more traumatic to chimpanzee than bonobo infants. But on the other hand the development of behaviors is expected to be very similar in both species. We observed eight mother–infant pairs of each species in several European zoos. Our preliminary research partially confirms that immature chimpanzees seem spatially more independent, spending more time at a larger distance from their mother than immature bonobos. However, the other data do not seem to support the hypothesis that bonobo infants show retardation of motor or social development. The development of solitary play, environmental exploration, social play, non-copulatory mounts and aggressive interactions do not differ between the species. Bonobo infants in general even groom other group members more than chimpanzee infants. We also found that older bonobo infants have more nipple contact than same aged chimpanzees and that the weaning process seems to end later for bonobos than for immature chimpanzee. Additionally, although immature bonobos show in general more signs of distress, our data suggest that the weaning period itself is more traumatic for chimpanzees.     

Spatial aspects of spontaneous object grouping by young chimpanzees(Pan troglodytes)

I report spontaneous spatial object grouping in five chimpanzees (Pan troglodytes)ranging from 1 to 4 years of age. I recorded subjects' spontaneous interactions with groups of objects, noting the spatial relations in the groupings and the constructive processes that the subjects adopted. Though one subject developed vertical stacks, none of them realized horizontal alignments or spatial correspondences between groups. All subjects showed consistent trends in their constructive processes toward manipulating objects in relation to the body: they increasingly manipulated objects globally, that is to say, they moved or held objects together with the same part of the body. They also increasingly placed objects on the body or in correspondence to their symmetrical body parts. The increasing importance assigned by chimpanzees to body- object relations over object- object relations contrasts with human developmental trends in the domain of manipulative space.     

Establishing the presence of a body temperature rhythm in chimpanzees (Pan troglodytes) using a tympanic membrane thermometer

Seven chimpanzees (Pan troglodytes) were trained to present their ears so that a tympanic nembrane thermometer could be inserted. Temperatures were collected from both ears of each subject every 3 hours for 72 consecutive hours. The presence of a body temperature rhythm, well documented in other mammals, was established. Each ear demonstrated its own rhythm, but the rhythms in both ears generally mirrored each other. Similarities in the temperature rhythms of cagemates were found. These data are the first evidence of a body temperature rhythm in chimpanzees, and they represent a non-invasive method of measuring the 24-hr rhythms in both human and non-human primates.     

Play behaviour and its effects on social development of common chimpanzees (Pan troglodytes)

The aim of the study was to monitor the social development of infant and juvenile common chimpanzees (Pan troglodytes) through their play behaviour at Taronga Zoo in Sydney in order to examine the possible effects of captivity (such as limited opportunities to play) on social development. Play behaviour was observed by focal animal sampling to determine individual differences, and their relationship to age, sex, and relatedness of the subjects. Analysis revealed marked individual variations in social, solitary, and object play behaviours indicative of a relatively well-balanced social and physical environment. Subjects showed a marked preference for play-partners of a different age compared to their own, and initiated interactions with similar frequency with members of both sexes. Many social-play dyads consisted of related individuals, and familiarity with prospective play-mates was the most decisive factor in social interactions.     

An apparatus and procedure for studying the choice component of foraging in a captive group of chimpanzees (Pan troglodytes)

An apparatus is described which was used to investigate the choice component of foraging in a captive group of chimpanzees maintained in a large, outdoor compound at the Yerkes Regional Primate Research Center Field Station. The utilization of more than one apparatus would allow the investigation of other ecological and psychological concepts in nonhuman primates housed under semi-natural conditions.     

Preliminary report on predatory behavior and meat sharing in tschego chimpanzees (Pan troglodytes troglodytes) in the Ndoki forest,northern Congo

Predatory behavior ofPan t. troglodytes in the Ndoki Forest was confirmed by both direct observation and fecal evidence. Eight out of 214 fecal samples (3.7%), collected during 16 months, contained vertebrate tissue. The prey species were a terrestrial bird, two monkey species including crowned guenon, a squirrel, and probably a pangolin. This rate suggested that predation in the Ndoki population can occur as frequently as in other populations. Chimpanzees were also directly observed to eat an infant crowned guenon, a hornbill, and a duiker. An adult female used a branch apparently in an attempt to drive out a hornbill from its nest hole, though no bird was observed to come out. Chimpanzees were attracted to meat, and were observed begging and sharing over the meat. Predatory behavior is common toPan andHomo, but not toGorilla, implying that the common ancestor of the former two genera acquired this behavior after separating from gorillas.     

Piagetian stage 5 in two infant chimpanzees (Pan troglodytes): The development of permanence of objects and the spatialization of causality

We investigated the level of cognitive development of two chimpanzee infants, both tested at 14 and 19 months of age, within the Piagetian framework of cognitive development. We administered tasks related to the understanding of object-concept—visible displacement tasks-and the operation of physical causality—the support problem-and observed responses similar to those of human infants. Both subjects reached stage 5 object-concept when they were 19 months of age: only at this time, in fact, were chimpanzees able to find the object wherever it was hidden. Stage 4 errors still characterized infants' performance when they were 14 months old. However, only one of the 19-month-old subjects was able to solve the support problem: she ignored the support when the goal object did not rest on it, showing that the understood the necessity of spatial contact between the target and the intermediary object. On the contrary, the other subject was not proficient in such a task because he drew the support even when the reward was placed beside it. At 19 months of age its level of causality still remained characteristic of the fourth stage.     

Chimpanzees (Pan troglodytes) use markers to monitor the movement of a hidden item

Four chimpanzees (Pan troglodytes) monitored the movement of hidden items in arrays of opaque cups. A chocolate candy was hidden in an array of four cups and temporarily presented paper markers indicated the location of the candy (which otherwise was not visible). These markers were either non-symbolic or symbolic (lexigram) stimuli that in other contexts acted as a label for the hidden candy, and the array was either rotated 180° after the marker was removed or the array remained in the same location. For three of four chimpanzees, performance was better than chance in all conditions and there was no effect of the type of marker. These experiments indicate that chimpanzees can track the movement of a hidden item in an array of identical cups even when they never see the item itself, but only see a temporarily presented marker for the location of that item. However, there was no benefit to the use of symbolic as opposed to non-symbolic stimuli in this performance.     

Chimpanzees' (Pan troglodytes) choice of prey among termites (macrotermitinae) in western Tanzania

This study examines factors affecting chimpanzees' preying on termites, especially their choice of prey species. Regular surveys of a large sample of termite-mounds in the Mahale Mountains, Tanzania, confirmed that chimpanzees of B Group obtainedMacrotermes, which were relatively uncommon, by the use of fishing-tools, but ignored the much more abundantOdontotermes. This preference appeared to reflectMacrotermes' more extended swarming period, greater accessibility, larger size, and less noxious taste than the soldiers ofOdontotermes. Similar factors probably underly the chimpanzees' choice ofMacrotermes at Gombe, butPseudacanthotermes spiniger are also common there, and their absence from the diet is less easily explained. In contrast, the chimpanzees of K Group at Mahale prey mainly onP. spiniger;Macrotermes are apparently absent, andP. spiniger appear to be more abundant, accessible, and palatable than the alternativeOdontotermes.     

Social parameters and urinary testosterone level in male chimpanzees (Pan troglodytes)

Studies investigating relationships between social parameters (such as dominance rank, rates of aggressive and sexual behaviors) and androgen (particularly, testosterone) levels in male primates have yielded inconsistent results. In the present study, we address the relationship between androgens, male dominance rank and rank-associated behaviors in two groups of captive chimpanzees, a species characterized by a pronounced dominance hierarchy between adult males. By combining behavioral observations with urinary testosterone (T) measurements, we found that the differences in T concentrations between males were small and not obviously related to their dominance rank. T levels were not related to the rates of initiated aggression and copulatory behavior, but a significant negative relationship between male T level and the rates of strong aggression received was apparent. Our findings, combined with those of others, suggest that any relationship between dominance rank and T depends upon the extent to which individual rank-associated behaviors (e.g. aggressive/sexual) are themselves related to T.     

Inversion effect in perception of human faces in a chimpanzee (Pan troglodytes)

Three experiments investigated the inversion effect in face perception by a chimpanzee (Pantroglodytes) under the matching-to-sample paradigm. The first two experiments addressed the inversion effect in the perception of human faces. In Experiment 1, the subject received identity matching using 104 photographs of faces and houses presented in four different orientations. The chimpanzee showed better accuracy when the faces were presented upright than when they were inverted. The inversion effect was not found for photographs of houses. In Experiment 2, the subject received rotational matching in which the sample and comparisons differed in orientation. The subject showed a clear inversion effect for faces but not for houses. Experiment 3 explored the hemispheric specialization of the face inversion effect with chimeric (artificially composed) faces. The subject showed no visual-field preference when the chimeric faces were presented as samples under nonreinforced probe testing, while the inversion effect was evident when the discrimination was based on the left part of the chimeric sample. The results suggested that the face-inversion was specific to the left visual field (i.e. right hemispheric processing). In general, these results were consistent with those found in humans in similar testing situations.     

Predation on mammals by the chimpanzee (Pan troglodytes)

With respect to prey selectivity and predation frequency, chimpanzees (Pan troglodytes) show local differences as well as diachronic variability within the same population. When data on predation from three long-term studies at Mahale, Gombe, and Tai are compared, some differences and similarities emerge; Mahale is more like Gombe than Tai in regard of prey selection but features of hunting at Tai with respect to predation frequency are not conspicuous. The most responsible factor for diversity in prey selectivity is a distinct “prey image” maintained by chimpanzees of different populations, although it is necessary to clarify in future studies why and how such tradition develops. Relative body size of chimpanzees to prey species and/or the degree of cooperation among members of a hunting party may explain the variability in prey size selected at each site, the latter influencing the frequency of successful hunts at the same time. Although various degrees of habituation and different sampling methods including artificial feeding might have obscured the real differences, recent data from the three populations do not seem to be biased greatly by such factors. Nevertheless, it is still difficult to make strict comparisons due to the lack of sufficient standardized data across the three populations on the frequency of hunting and predation. It is suggested that the size or demographic trend of a chimpanzee unit-group, especially the number of adult males included, necessarily influences its hunting frequency as well as its prey profile. It is also suggested that factors which bring these males together into a party (e.g. fruit abundance, swollen females, conflict between unit-groups etc.) strongly affect theactual hunting and kill rates. Other possible factors responsible for the local differences are forest structure (e.g. tree height), skilful “hero” chimpanzees, and competition with sympatric carnivorous animals. A total of at least 32 species have been recorded as prey mammals of chimpanzees from 12 study sites and the most common prey mammals are primates (18 species), of which 13 species are forest monkeys. Forest monkeys, colobine species in particular, are often the most common victims of the predation by chimpanzees at each site. We may point out a tendency toward selective hunting for the forest monkeys in terms of the selectivity of prey fauna among all three subspecies of chimpanzees, including populations living in drier environment. The mode of chimpanzee hunting seems to correspond to the highest available biomass of gregarious, arboreal monkeys in the forest, colobine species in particular. In contrast, bonobos (P. paniscus) are less carnivorous than chimpanzees, only rarely preying on a few species of small mammals. The sharp contrast of the two allied species in their predatory tendencies appears to have something to do with the differences in the structure of primary production between their habitats.     

Captive breeding, paternity determination, and genetic variation in chimpanzees (Pan troglodytes) in the Australasian region

DNA “fingerprinting” using polymorphic (CA)-repeat microsatellite markers was used to quantify the level of genetic variation present in chimpanzees (Pan troglodytes) in the Australasian region. These markers were also used to determine the paternity of chimpanzees born at Taronga Zoo over a 20-year period. The results suggested that the dominant male in the colony was responsible for siring most, but not all, of the offspring. Where the dominant male was excluded from paternity, the sire was identifiable if all candidate males were available for typing. This enabled us to prove the captive origin of offspring born in the colony during this period. Thus, microsatellite analysis was a useful tool for assignment of familial relationships and improving genetic management of breeding colonies.     

A longitudinal study on hand and wrist skeletal maturation in chimpanzees ( Pan troglodytes), with emphasis on growth in linear dimensions

Skeletal maturation in the chimpanzee hand and wrist (the RUS system; radius, ulna, and short bones) was studied both longitudinally and cross-sectionally. Maturity states were evaluated in each of the 13 bones of the RUS system based on the TW2 method (Tanner and Whitehouse method), and the RUS score was calculated by the summation of scores for these bones. Individual variation was examined by means of residual curves and pseudo-velocity curves of RUS score and anterior trunk length (ATL). Norms of the age change pattern in RUS skeletal maturation and the growth of ATL were determined for each sex, and the relationships among ATL growth and skeletal and reproductive maturation were examined. We found a fairly good relationship between ATL growth and RUS skeletal maturation. Comparison of growth and development between humans and chimpanzees showed that growth characteristics are coupled with each other at puberty in male chimpanzees and in both sexes of humans. Although nutritional condition influenced ATL growth in infancy, it had no effect on the RUS maturational process. Social relationships appeared to influence both ATL growth and RUS maturation. Analyses on relationships between RUS skeletal maturation, ATL growth, and reproductive maturation, showed that RUS skeletal maturation is a good indicator of "physiological age".     

Do chimpanzees cooperate in a learning task?

The aim of this study was to assess the ability of chimpanzees (Pan troglodytes) to cooperate in an instrumental task. A specially constructed fruit distributor was presented to a group of six captive chimpanzees. A cooperative response required two chimpanzees: both had to pull a handle simultaneously to make a fruit fall into the cage. The dominant male of the group and an infant produced most of the operant responses, and the male got nearly all the fruits. Other conspecifics avoided the dominant male at the apparatus. Social influences appear to limit the possibility of co-operation between individuals because a certain level of interindividual tolerance is required. The results revealed a significant increase in the number of pulls each time both chimpanzees were together at the apparatus. Operant chimpanzees learn to coordinate their actions in time and space.     

Behavioral Adaptation of Pan troglodytes troglodytes

As wild primate populations decline, numbers of orphaned primates, sanctuaries, and attempts to release primates back to the natural environment increase. Release projects frequently are poorly documented despite IUCN guidelines recommending post-release monitoring and systematic data collection as central to the process. Since 1996, Habitat Ecologique et Liberté des Primates (HELP) has been releasing wild-born orphaned chimpanzees into natural habitat in the Conkouati-Douli National Park, Republic of Congo. HELP developed a post-release monitoring system as an integral component. We present activity budgets and diet of released chimpanzees, and compared them to those of wild chimpanzee, as primary indicators of successful release. Feeding, moving, and resting dominated activity budgets, reflecting the overall patterns in wild populations. Diet was diverse and dominated by fruit, and the released chimpanzees showed specialization on a smaller number of species, as in many wild communities. The high survival rates of the chimpanzees and overall success of the release program are attributed to careful planning and post-release support facilitated via the monitoring process. Systematic post-release data collection monitoring has confirmed that wild-born chimpanzees can adjust behaviorally and nutritionally to the wild. Survival statistics of the reintroduced chimpanzees—confirmed 56%, possible 88%— reflect the behavioral adaptability.2nd revision March 11, 2005An erratum to this article can be found at     

Food Supply and Chimpanzee (Pan troglodytes schweinfurthii) Party Size in the Budongo Forest Reserve,Uganda

A central issue in socioecology is the nature of the relationship between an organism's environment and its social structure. In chimpanzees, the fission-fusion social system is thought to minimize feeding competition for primary dietary components: ephemeral, dispersed patches of ripe fruit. Intragroup feeding competition is thought to force individuals into small parties. Informal observations in the Sonso region of the Budongo forest had suggested that in this habitat, food supply was such that feeding competition was less important in determining grouping patterns than elsewhere. We used data collected on food supply and party sizes over a 4-year period to investigate this suggestion. In accord with theoretical expectation, sizes of foraging parties fluctuated with the size of food patches. However, party sizes showed either negative or no relationship with habitat-wide measures of food abundance. Likewise party sizes showed little relationship to overall measures of food dispersion. For important dietary items, both fruit and leaves had patchy distributions, though the degree of clumping was not strong, and fruit was not more clumped than leaves. Generally, abundant food appeared to be less patchy, and chimpanzees appeared to use more patches as food became more abundant rather than forming larger parties. We suggest that both dispersal and abundance need to be considered when investigating the impact of food supply on grouping patterns, and that the importance of food as a factor in determining chimpanzee grouping patterns declines with increasing levels of abundance.     

Body size and proportions in chimpanzees,with special reference toPan troglodytes schweinfurthii from Gombe National Park,Tanzania

Body weight, cranial capacity, linear and joint area data from ten free-ranging adult chimpanzees from Gombe National Park, Tanzania with known life histories allow study of variation in a local population and comparison to other populations ofPan troglodytes and toPan paniscus. Because individuals in the Gombe population are small compared to other common chimpanzees, they provide a useful comparison toPan paniscus. Body weight and some linear dimensions overlap withPan paniscus. However, cranial capacity, tooth size, and body proportions of Gombe individuals lie within the range of otherPan troglodytes and are distinct fromPan paniscus.     

Severe Aggression Among Female Pan troglodytes schweinfurthii at Gombe National Park, Tanzania

Aggression is generally more severe between males than between females because males gain greater payoffs from escalated aggression. Males that successfully defeat rivals may greatly increase their access to fertile females. Because female reproductive success depends on long-term access to resources, competition between females is often sustained but low key because no single interaction leads to a high payoff. Nonetheless, escalated aggression can sometimes immediately improve a female’s reproductive success. Resisting new immigrants can reduce feeding competition, and infanticide of other females’ young can increase a female’s access to resources. East African chimpanzees live in fission-fusion communities in which females occupy overlapping core areas. Growing evidence indicates that reproductive success correlates with core area quality, and that females compete for long-term access to core areas. Here we document 5 new cases of severe female aggression in the context of such competition: 2 attacks by resident females on an immigrant female, a probable intracommunity infanticide, and 2 attacks on a female and her successive newborn infants by females whose core areas overlapped hers. The cases provide further evidence that females are occasionally as aggressive as males. Factors influencing the likelihood and severity of such attacks include rank and size differences and the presence of dependable allies. Counterstrategies to the threat of female aggression include withdrawing from others around the time of parturition and seeking male protection. We also discuss an unusual case of a female taking the newborn infant of another, possibly to protect it from a potentially infanticidal female.