Abstract: The processing of Kanizsa-square illusory figures was studied in two experiments with four humans and two chimpanzees. Subjects of the two species were initially trained to select a Kanizsa-square illusory figure presented in a computerized two-alternative forced choice task. After training, adding narrow closing segments to the pacman inducers that composed the Kanisza illusory figures lowered performance in both chimpanzees and humans, suggesting that the discrimination could be controlled by the perception of illusory forms. A second experiment assessed transfer of performance with five sets of figures in which the size of the inducers and their separation were manipulated. Only for chimpanzees was performance directly controlled by separation, suggesting that chimpanzees are more sensitive than humans to the separation between visual elements.

Abstract: Chimpanzees follow conspecific and human gaze direction reliably in some situations, but very few chimpanzees reliably use gaze direction or other communicative signals to locate hidden food in the object-choice task. Three studies aimed at exploring factors that affect chimpanzee performance in this task are reported. In the first study, vocalizations and other noises facilitated the performance of some chimpanzees (only a minority). In the second study, various behavioral cues were given in which a human experimenter either touched, approached, or actually lifted and looked under the container where the food was hidden. Each of these cues led to enhanced performance for only a very few individuals. In the third study – a replication with some methodological improvements of a previous experiment – chimpanzees were confronted with two experimenters giving conflicting cues about the location of the hidden food, with one of them (the knower) having witnessed the hiding process and the other (the guesser) not. In the crucial test in which a third experimenter did the hiding, no chimpanzee found the food at above chance levels. Overall, in all three studies, by far the best performers were two individuals who had been raised in infancy by humans. It thus seems that while chimpanzees are very good at “behavior reading” of various sorts, including gaze following, they do not understand the communicative intentions (informative intentions) behind the looking and gesturing of others – with the possible exception of enculturated chimpanzees, who still do not understand the differential significance of looking and gesturing done by people who have different knowledge about states of affairs in the world.

Abstract: Current research on face processing in primates has focused on a few species, mostly macaques and chimpanzees; to date, only one New World monkey, the squirrel monkey, has been tested. We explored face processing, and the inversion effect in particular, in a New World primate species, the cotton-top tamarin (Saguinus oedipus). In phase 1 of our study, we trained subjects to discriminate between two faces and two scrambled faces; we then presented the tamarins with a series of novel probes in order to determine the features underlying classification. Results showed that the tamarins relied on the external contour of the face for discrimination more than the internal features and their configuration. Statistical analyses revealed no differences in accuracy or response times to upright versus inverted stimuli, and thus no inversion effect. In phase 2, we provided subjects with additional training on the face versus scrambled face discrimination task in order to focus their attention on the configuration of the internal features. Accuracy data revealed individual differences in how tamarins classified these stimuli, even though each subject was trained in the same way. In phase 3, we tested for generalization to a new set of face stimuli, as well as for the capacity to show an inversion effect. For one subject who attended to the configuration of internal features, we found significant evidence of generalization, but no evidence for an inversion effect.

Abstract: The use of leaves for drinking water by wild chimpanzees ( Pan troglodytes verus) at Bossou, Guinea, was observed intensively. The natural hollow of a tree, used by chimpanzees, was filled up with fresh water every morning. Seventy episodes of leaf-using behavior by 14 chimpanzees were directly observed and video-recorded. The chimpanzees at Bossou most frequently (70.3%) used a particular kind of leaf, Hybophrynium braunianum as tool material. The chimpanzees folded one or more leaves in the mouth. This technique, “leaf folding”, was observed more frequently (57.9 %) than “leaf sponge” or “leaf spoon”. Chimpanzees began to perform this behavior at about 2.5 years old. Infant chimpanzees showed more frequent observations of others (especially their mothers) using leaves before trying to drink water with leaves. Both observation and trial and error might be necessary for the acquisition of this tool-use behavior.

Abstract: Abstract  Most studies of spatial memory in primates focus on species that inhabit large home ranges and have dispersed, patchy resources. Researchers assume that primates use memory to minimize distances traveled between resources. We investigated the use of spatial memory in a group of six white-faced sakis (Pithecia pithecia) on 12.8-ha Round Island, Guri Lake, Venezuela during a period of fruit abundance. The sakis movements were analyzed with logistic regressions, a predictive computer model and a computer model that simulates movements. We considered all the resources available to the sakis and compared observed distances to predicted distances from a computer model for foragers who know nothing about the location of resources. Surprisingly, the observed distances were four times greater than the predicted distances, suggesting that the sakis passed by a majority of the available fruit trees without feeding. The odds of visiting a food tree, however, were significantly increased if the tree had been visited in the previous 3 days and had more than 100 fruit. The sakis preferred resources were highly productive fruit trees, Capparis trees, and trees with water holes. They traveled efficiently to these sites. The sakis choice of feeding sites indicate that they combined knowledge acquired by repeatedly traveling through their home range with “what” and “where” information gained from individual visits to resources. Although the sakis foraging choices increased the distance they traveled overall, choosing more valued sites allowed the group to minimize intragroup feeding competition, maintain intergroup dominance over important resources, and monitor the state of resources throughout their home range. The sakis foraging decisions appear to have used spatial memory, elements of episodic-like memory and social and nutritional considerations.