Book contents
- The Chimpanzees of the Taï Forest
- The Chimpanzees of the Taï Forest
- Copyright page
- Dedication
- Contents
- Contributors
- Preface
- Acknowledgements
- 1 War and peace in the Taï chimpanzee forest: running a long-term chimpanzee research project
- 2 Developments in statistical methods applied over four decades of research in the Taï Chimpanzee Project
- 3 Observation protocol and long-term data collection in Taï
- 4 The Wild Chimpanzee Foundation (WCF) and the Taï Chimpanzee Project (TCP)
- 5 Insights from genetic analyses of the Taï chimpanzees
- 6 Endocrinological analyses at Taï
- 7 Chimpanzee behavioural diversity and the contribution of the Taï Chimpanzee Project
- 8 An energetic model of foraging optimization: wild chimpanzee hammer selection for nut-cracking
- 9 Demography and life history of five chimpanzee communities in Taï National Park
- 10 Adoption in the Taï chimpanzees: costs, benefits and strong social relationships
- 11 Spatial integration of unusually high numbers of immigrant females into the South Group: further support for the bisexually bonded model in Taï chimpanzees
- 12 Forty years striving to capture culture among the Taï chimpanzees
- 13 Cultural diversity of nut-cracking behaviour between two populations of wild chimpanzees (Pan troglodytes verus) in the Côte d’Ivoire
- 14 Ecological and social influences on rates of social play in immature wild chimpanzees (Pan troglodytes verus)
- 15 Long-term diet of the chimpanzees (Pan troglodytes verus) in Taï National Park: interannual variations in consumption
- 16 Why Taï mangabeys do not use tools to crack nuts like sympatric-living chimpanzees: a cognitive limitation on monkey feeding ecology
- 17 Providing research for conservation from long-term field sites
- 18 Rank changes in female chimpanzees in Taï National Park
- 19 Effects of large-scale knockouts on chimpanzee association networks
- 20 Why do the chimpanzees of the Taï Forest share meat? The value of bartering, begging and hunting
- 21 Group-specific social dynamics affect urinary oxytocin levels in Taï male chimpanzees
- 22 The chimpanzees of the Taï Forest as models for hominine microorganism ecology and evolution
- 23 Acute infectious diseases occurring in the Taï chimpanzee population: a review
- 24 Why does the chimpanzee vocal repertoire remain poorly understood and what can be done about it?
- 25 Evidence for sexual dimorphism in chimpanzee vocalizations: a comparison of male and female call production and acoustic parameters
- 26 Gestural usage and development in two chimpanzee groups of different subspecies (Pan troglodytes verus/P.t. schweinfurthii)
- 27 Spatial cognitive abilities in foraging chimpanzees
- 28 Temporal cognition in Taï chimpanzees
- Index
- References
24 - Why does the chimpanzee vocal repertoire remain poorly understood and what can be done about it?
Published online by Cambridge University Press: 25 November 2019
Book contents
- The Chimpanzees of the Taï Forest
- The Chimpanzees of the Taï Forest
- Copyright page
- Dedication
- Contents
- Contributors
- Preface
- Acknowledgements
- 1 War and peace in the Taï chimpanzee forest: running a long-term chimpanzee research project
- 2 Developments in statistical methods applied over four decades of research in the Taï Chimpanzee Project
- 3 Observation protocol and long-term data collection in Taï
- 4 The Wild Chimpanzee Foundation (WCF) and the Taï Chimpanzee Project (TCP)
- 5 Insights from genetic analyses of the Taï chimpanzees
- 6 Endocrinological analyses at Taï
- 7 Chimpanzee behavioural diversity and the contribution of the Taï Chimpanzee Project
- 8 An energetic model of foraging optimization: wild chimpanzee hammer selection for nut-cracking
- 9 Demography and life history of five chimpanzee communities in Taï National Park
- 10 Adoption in the Taï chimpanzees: costs, benefits and strong social relationships
- 11 Spatial integration of unusually high numbers of immigrant females into the South Group: further support for the bisexually bonded model in Taï chimpanzees
- 12 Forty years striving to capture culture among the Taï chimpanzees
- 13 Cultural diversity of nut-cracking behaviour between two populations of wild chimpanzees (Pan troglodytes verus) in the Côte d’Ivoire
- 14 Ecological and social influences on rates of social play in immature wild chimpanzees (Pan troglodytes verus)
- 15 Long-term diet of the chimpanzees (Pan troglodytes verus) in Taï National Park: interannual variations in consumption
- 16 Why Taï mangabeys do not use tools to crack nuts like sympatric-living chimpanzees: a cognitive limitation on monkey feeding ecology
- 17 Providing research for conservation from long-term field sites
- 18 Rank changes in female chimpanzees in Taï National Park
- 19 Effects of large-scale knockouts on chimpanzee association networks
- 20 Why do the chimpanzees of the Taï Forest share meat? The value of bartering, begging and hunting
- 21 Group-specific social dynamics affect urinary oxytocin levels in Taï male chimpanzees
- 22 The chimpanzees of the Taï Forest as models for hominine microorganism ecology and evolution
- 23 Acute infectious diseases occurring in the Taï chimpanzee population: a review
- 24 Why does the chimpanzee vocal repertoire remain poorly understood and what can be done about it?
- 25 Evidence for sexual dimorphism in chimpanzee vocalizations: a comparison of male and female call production and acoustic parameters
- 26 Gestural usage and development in two chimpanzee groups of different subspecies (Pan troglodytes verus/P.t. schweinfurthii)
- 27 Spatial cognitive abilities in foraging chimpanzees
- 28 Temporal cognition in Taï chimpanzees
- Index
- References
Summary
After decades of research, the origins of human speech remain little understood. One undoubted problem is that the vocal repertoires of humans’ closest living relatives, the apes, remain poorly described. Given that the evolution of language has left few fossils, many researchers interested in this question adopt a comparative approach, examining differences and consistencies between human and animal communication. However, comparisons will remain limited in the absence of a comprehensive analysis of the vocal repertoires of the other extant apes, especially of our two closest living relatives, the chimpanzee and bonobo. After years of observing and conducting field experiments with both western and eastern chimpanzees, I posit several reasons why a comprehensive analysis of the chimpanzee vocal repertoire has not yet been completed, in spite of 45 years of research, and what can be done to remedy this situation. I also tabulate cross-site consensus in call categorization, associated contexts of usage and potential call functions. I also note cross-site variation in presence and absence of vocalizations.
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- The Chimpanzees of the Taï Forest40 Years of Research, pp. 394 - 409Publisher: Cambridge University PressPrint publication year: 2019
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