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The Facial Action Coding System (FACS) is a widely recognised coding scheme for analysing human facial behaviour, providing an objective method to quantify discrete movements associated with facial muscles, known as Action Units (AUs), and reducing subjective bias. FACS has been adapted for nine other taxa, including apes, macaques, and domestic animals, but not yet bonobos. To carry out cross species studies of facial behaviours within and beyond apes, it is essential to include bonobos. Hence, we aimed at adapting FACS for bonobos. We followed a similar methodology as in previous FACS adaptations: first, we examined the facial muscular plan of bonobos from previously published dissections. Given the similarity between bonobo and chimpanzee musculature, we tested if ChimpFACS for chimpanzees could be applied to bonobos. Second, we used ChimpFACS to analyse spontaneous facial behaviour in bonobos through videos recorded in various contexts. Third, we noted any differences in appearance changes between the AUs included in ChimpFACS and the AUs observed in bonobos. Our findings showed that bonobos exhibit all the facial movements observed in chimpanzees, and thus ChimpFACS can reliably be applied to bonobos. Bonobos presented a diverse repertoire of 28 facial movements (22 AUs, three Action Descriptors, and three Ear Action Descriptors). Although the range of facial movement is lower than in humans, bonobo's potential for facial movement is comparable to that of chimpanzees, underscoring the significance of this behaviour modality during social interactions for both species. The ChimpFACS Extension for bonobos is an objective coding scheme for measuring facial movements in bonobos, designed to be used in conjunction with ChimpFACS. This coding scheme extension will allow us to better understand bonobos' behaviour and communication, with practical applications for assessing their welfare, particularly in human care. It also provides a framework for comparing primate species, contributing to insights into the origin and evolution of facial emotion and communication.
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http://dx.doi.org/10.7717/peerj.19484 | DOI Listing |
Virology
August 2025
Department of Cell & Chemical Biology, Leiden University Medical Center, Leiden, the Netherlands. Electronic address:
Many adenovirus (AdV) species have been isolated from human and non-human primates. Here we describe the isolation of a new AdV from a western lowland gorilla held captive in a zoo. Analysis of the genome sequence demonstrated that this virus is a member of the Mastadenovirus genus, but markedly distinct from all previously described species.
View Article and Find Full Text PDFZoo Biol
September 2025
Department of Ecology, Evolution, & Organismal Biology, Kennesaw State University, Kennesaw, Georgia, USA.
For social animals, group living can serve to buffer against stressors. However, changes in the social environment may also represent a stressor leading to changes in glucocorticoids-hormones responsible for maintaining homeostasis under stressful conditions. We studied glucocorticoids in captive bonobos (Pan paniscus), a social species of great ape with a complex social organization.
View Article and Find Full Text PDFR Soc Open Sci
August 2025
Department for Primate Cognition, Johann-Friedrich-Blumenbach Institute, Georg-August-Universität Göttingen, Göttingen, Niedersachsen, Germany.
Evaluating others' prosocial tendencies can benefit individuals by allowing them to interact with prosocial individuals and avoid antisocial ones. The ontogeny of humans' strong prosocial preference has been widely investigated using the hill paradigm. Infants' preference for helper over hinderer agents was measured after they watched a scene in which the helper agent pushed a climber up a hill while the hinderer agent pushed the climber down the hill.
View Article and Find Full Text PDFProc Biol Sci
August 2025
Department of Psychological & Brain Sciences, Johns Hopkins University, Baltimore, MD, USA.
Humans are adept at navigating the social world in part because we flexibly map the locations and identities of agents around us. While field studies suggest primates can track individual conspecifics, controlled experiments are needed to determine the complexity of this capacity and isolate the underlying representations. Across five object-choice tasks, we show that our closest relative, a bonobo (Kanzi), can concurrently track the locations and identities of multiple (specifically, two) hidden agents (Experiment 1), that this capacity deploys mental representations rather than tracking agents' last observed locations (Experiment 2), and that these representations can integrate visual or auditory signatures of identity (Experiment 3).
View Article and Find Full Text PDFCell Rep
August 2025
Behavioural Ecology and Ecophysiology Research Group, Department of Biology, University of Antwerp, 2610 Antwerp, Belgium; Zoo Antwerp Centre for Research and Conservation, Royal Zoological Society of Antwerp, 2018 Antwerp, Belgium. Electronic address:
In great apes, the gut bacteriome shapes key physiological functions and is influenced by both the exposome and the host. Yet, isolating these independent contributions remains challenging. We sequenced 644 fecal samples from 212 wild and zoo-housed bonobos (Pan paniscus), matched with detailed data collection on host and exposome factors.
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