Primate and Human Evolution Susan Cachel New York: Cambridge University Press, 2006, 469 Pp
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EAZA Best Practice Guidelines Bonobo (Pan Paniscus)
EAZA Best Practice Guidelines Bonobo (Pan paniscus) Editors: Dr Jeroen Stevens Contact information: Royal Zoological Society of Antwerp – K. Astridplein 26 – B 2018 Antwerp, Belgium Email: [email protected] Name of TAG: Great Ape TAG TAG Chair: Dr. María Teresa Abelló Poveda – Barcelona Zoo [email protected] Edition: First edition - 2020 1 2 EAZA Best Practice Guidelines disclaimer Copyright (February 2020) by EAZA Executive Office, Amsterdam. All rights reserved. No part of this publication may be reproduced in hard copy, machine-readable or other forms without advance written permission from the European Association of Zoos and Aquaria (EAZA). Members of the European Association of Zoos and Aquaria (EAZA) may copy this information for their own use as needed. The information contained in these EAZA Best Practice Guidelines has been obtained from numerous sources believed to be reliable. EAZA and the EAZA APE TAG make a diligent effort to provide a complete and accurate representation of the data in its reports, publications, and services. However, EAZA does not guarantee the accuracy, adequacy, or completeness of any information. EAZA disclaims all liability for errors or omissions that may exist and shall not be liable for any incidental, consequential, or other damages (whether resulting from negligence or otherwise) including, without limitation, exemplary damages or lost profits arising out of or in connection with the use of this publication. Because the technical information provided in the EAZA Best Practice Guidelines can easily be misread or misinterpreted unless properly analysed, EAZA strongly recommends that users of this information consult with the editors in all matters related to data analysis and interpretation. -
Order Representations + a Rich Memetic Substrate
Language Needs A 2nd Order Representations + A Rich Memetic Substrate Joanna J. Bryson ([email protected]) Artificial models of natural Intelligence (AmonI) Group, University of Bath, England, UK Recent research has shown that human semantics can be 2nd-ord. soc. rep. no 2nd-ord reps replicated by surprisingly simple statistical algorithms for vocal imit. people birds memorizing the context in which words occur (McDonald no voc. imit. other primates most animals and Lowe, 1998; Landauer and Dumais, 1997). Assum- ing one accepts the point that semantics is the way that the word is used (which cannot be argued in one page, but see Figure 1: Human-like cultural evolution might require both Wittgenstein (1958) or Quine (1960), and which is the un- a rich memetic substrate as provided by vocal imitation, and derlying assumption of memetics) then why wouldn’t more the capacity for second order social representations. species have supported the evolution of this useful system of rapidly evolving cultural intelligence? Recent work in primatology tells us three relevant facts. might have evolved a sign language as rich as our vocal one. First, we know that apes and even monkeys do have cul- However, if I am correct, and the trick is that the richness of ture (de Waal and Johanowicz, 1993; Whiten et al., 1999). the substrate representing the strictly semantic, ungrounded That is, behavior is reliably and consistently transmitted be- cultural transmission is the key, then we now have an ex- tween individuals by non-genetic means. So we know that planation for why other primates don’t share our level of the question is not “why doesn’t animal culture exist”, but culture. -
New Fossil Discovery Illuminates the Lives of the Earliest Primates 24 February 2021
New fossil discovery illuminates the lives of the earliest primates 24 February 2021 Royal Society Open Science. "This discovery is exciting because it represents the oldest dated occurrence of archaic primates in the fossil record," Chester said. "It adds to our understanding of how the earliest primates separated themselves from their competitors following the demise of the dinosaurs." Chester and Gregory Wilson Mantilla, Burke Museum Curator of Vertebrate Paleontology and University of Washington biology professor, were co-leads on this study, where the team analyzed fossilized teeth found in the Hell Creek area of northeastern Montana. The fossils, now part of the collections at the University of California Museum of Paleontology, Berkeley, are estimated to be 65.9 Shortly after the extinction of the dinosaurs, the earliest million years old, about 105,000 to 139,000 years known archaic primates, such as the newly described after the mass extinction event. species Purgatorius mckeeveri shown in the foreground, quickly set themselves apart from their competition -- like Based on the age of the fossils, the team estimates the archaic ungulate mammal on the forest floor -- by that the ancestor of all primates (the group specializing in an omnivorous diet including fruit found including plesiadapiforms and today's primates up in the trees. Credit: Andrey Atuchin such as lemurs, monkeys, and apes) likely emerged by the Late Cretaceous—and lived alongside large dinosaurs. Stephen Chester, an assistant professor of anthropology and paleontologist at the Graduate Center, CUNY and Brooklyn College, was part of a team of 10 researchers from across the United States who analyzed several fossils of Purgatorius, the oldest genus in a group of the earliest-known primates called plesiadapiforms. -
Proposal for Inclusion of the Chimpanzee
CMS Distribution: General CONVENTION ON MIGRATORY UNEP/CMS/COP12/Doc.25.1.1 25 May 2017 SPECIES Original: English 12th MEETING OF THE CONFERENCE OF THE PARTIES Manila, Philippines, 23 - 28 October 2017 Agenda Item 25.1 PROPOSAL FOR THE INCLUSION OF THE CHIMPANZEE (Pan troglodytes) ON APPENDIX I AND II OF THE CONVENTION Summary: The Governments of Congo and the United Republic of Tanzania have jointly submitted the attached proposal* for the inclusion of the Chimpanzee (Pan troglodytes) on Appendix I and II of CMS. *The geographical designations employed in this document do not imply the expression of any opinion whatsoever on the part of the CMS Secretariat (or the United Nations Environment Programme) concerning the legal status of any country, territory, or area, or concerning the delimitation of its frontiers or boundaries. The responsibility for the contents of the document rests exclusively with its author. UNEP/CMS/COP12/Doc.25.1.1 PROPOSAL FOR THE INCLUSION OF CHIMPANZEE (Pan troglodytes) ON APPENDICES I AND II OF THE CONVENTION ON THE CONSERVATION OF MIGRATORY SPECIES OF WILD ANIMALS A: PROPOSAL Inclusion of Pan troglodytes in Appendix I and II of the Convention on the Conservation of Migratory Species of Wild Animals. B: PROPONENTS: Congo and the United Republic of Tanzania C: SUPPORTING STATEMENT 1. Taxonomy 1.1 Class: Mammalia 1.2 Order: Primates 1.3 Family: Hominidae 1.4 Genus, species or subspecies, including author and year: Pan troglodytes (Blumenbach 1775) (Wilson & Reeder 2005) [Note: Pan troglodytes is understood in the sense of Wilson and Reeder (2005), the current reference for terrestrial mammals used by CMS). -
The Evolution of Human Vocal Emotion
EMR0010.1177/1754073920930791Emotion ReviewBryant 930791research-article2020 SPECIAL SECTION: EMOTION IN THE VOICE Emotion Review Vol. 13, No. 1 (January 2021) 25 –33 © The Author(s) 2020 ISSN 1754-0739 DOI:https://doi.org/10.1177/1754073920930791 10.1177/1754073920930791 The Evolution of Human Vocal Emotion https://journals.sagepub.com/home/emr Gregory A. Bryant Department of Communication, Center for Behavior, Evolution, and Culture, University of California, Los Angeles, USA Abstract Vocal affect is a subcomponent of emotion programs that coordinate a variety of physiological and psychological systems. Emotional vocalizations comprise a suite of vocal behaviors shaped by evolution to solve adaptive social communication problems. The acoustic forms of vocal emotions are often explicable with reference to the communicative functions they serve. An adaptationist approach to vocal emotions requires that we distinguish between evolved signals and byproduct cues, and understand vocal affect as a collection of multiple strategic communicative systems subject to the evolutionary dynamics described by signaling theory. We should expect variability across disparate societies in vocal emotion according to culturally evolved pragmatic rules, and universals in vocal production and perception to the extent that form–function relationships are present. Keywords emotion, evolution, signaling, vocal affect Emotional communication is central to social life for many ani- 2001; Pisanski, Cartei, McGettigan, Raine, & Reby, 2016; mals. Beginning with Darwin -
Evolution of Grasping Among Anthropoids
doi: 10.1111/j.1420-9101.2008.01582.x Evolution of grasping among anthropoids E. POUYDEBAT,* M. LAURIN, P. GORCE* & V. BELSà *Handibio, Universite´ du Sud Toulon-Var, La Garde, France Comparative Osteohistology, UMR CNRS 7179, Universite´ Pierre et Marie Curie (Paris 6), Paris, France àUMR 7179, MNHN, Paris, France Keywords: Abstract behaviour; The prevailing hypothesis about grasping in primates stipulates an evolution grasping; from power towards precision grips in hominids. The evolution of grasping is hominids; far more complex, as shown by analysis of new morphometric and behavio- palaeobiology; ural data. The latter concern the modes of food grasping in 11 species (one phylogeny; platyrrhine, nine catarrhines and humans). We show that precision grip and precision grip; thumb-lateral behaviours are linked to carpus and thumb length, whereas primates; power grasping is linked to second and third digit length. No phylogenetic variance partitioning with PVR. signal was found in the behavioural characters when using squared-change parsimony and phylogenetic eigenvector regression, but such a signal was found in morphometric characters. Our findings shed new light on previously proposed models of the evolution of grasping. Inference models suggest that Australopithecus, Oreopithecus and Proconsul used a precision grip. very old behaviour, as it occurs in anurans, crocodilians, Introduction squamates and several therian mammals (Gray, 1997; Grasping behaviour is a key activity in primates to obtain Iwaniuk & Whishaw, 2000). On the contrary, the food. The hand is used in numerous activities of manip- precision grip, in which an object is held between the ulation and locomotion and is linked to several func- distal surfaces of the thumb and the index finger, is tional adaptations (Godinot & Beard, 1993; Begun et al., usually viewed as a derived function, linked to tool use 1997; Godinot et al., 1997). -
Phylogenomic Evidence of Adaptive Evolution in the Ancestry of Humans
Phylogenomic evidence of adaptive evolution in the ancestry of humans Morris Goodmana,b,1 and Kirstin N. Sternera aCenter for Molecular Medicine and Genetics and bDepartment of Anatomy and Cell Biology, Wayne State University School of Medicine, Detroit, MI 48201 In Charles Darwin’s tree model for life’s evolution, natural selection nomic studies of human evolution. We then highlight the concepts adaptively modifies newly arisen species as they branch apart from that motivate our own efforts and discuss how phylogenomic evi- their common ancestor. In accord with this Darwinian concept, the dence has enhanced our understanding of adaptive evolution in the phylogenomic approach to elucidating adaptive evolution in genes ancestry of modern humans. and genomes in the ancestry of modern humans requires a well supported and well sampled phylogeny that accurately places Darwin’s Views humans and other primates and mammals with respect to one In The Descent of Man, and Selection in Relation to Sex (5), Charles another. For more than a century, first from the comparative immu- Darwin suggested that Africa was the birthplace for humankind. nological work of Nuttall on blood sera and now from comparative The following five passages encapsulate for us Darwin’s thinking genomic studies, molecular findings have demonstrated the close about the place of humans in primate phylogeny and about the kinship of humans to chimpanzees. The close genetic correspond- uniqueness of modern humans. ence of chimpanzees to humans and the relative shortness of our evolutionary separation suggest that most distinctive features of If the anthropomorphous apes be admitted to form a natural subgroup, then as man agrees with them, not only in all those the modern human phenotype had already evolved during our characters which he possesses in common with the whole Cata- ancestry with chimpanzees. -
Oxytocin Is a Nonapeptide Involved in a Wide Range of Physiologic OXT Activity Depends on Adequate Interaction with Its Unique and Behavioral Functions
Evolutionary pattern in the OXT-OXTR system in primates: Coevolution and positive selection footprints Pedro Vargas-Pinillaa,1, Vanessa Rodrigues Paixão-Côrtesa,1, Pamela Paréa, Luciana Tovo-Rodriguesa, Carlos Meton de Alencar Gadelha Vieiraa, Agatha Xaviera, David Comasb, Alcides Pissinattic, Marialva Sinigagliaa, Maurício Menegatti Rigoa, Gustavo Fioravanti Vieiraa, Aldo B. Luciond, Francisco Mauro Salzanoa,2, and Maria Cátira Bortolinia,2 aDepartamento de Genética, Instituto de Biociências, Universidade Federal do Rio Grande do Sul, 91501-970 Porto Alegre, RS, Brazil; bInstitut de Biologia Evolutiva, Departament de Ciències Experimentals i de la Salut, Universitat Pompeu Fabra, 08003 Barcelona, Spain; cCentro de Primatologia do Rio de Janeiro, 20940-200 Rio de Janeiro, RJ, Brazil; and dDepartamento de Fisiologia, Instituto de Ciências Básicas da Saúde, Universidade Federal do Rio Grande do Sul, 90050-170 Porto Alegre, RS, Brazil Contributed by Francisco Mauro Salzano, November 26, 2014 (sent for review July 11, 2014; reviewed by Guido Barbujani and Rafal Slusarz) Oxytocin is a nonapeptide involved in a wide range of physiologic OXT activity depends on adequate interaction with its unique and behavioral functions. Until recently, it was believed that an receptor, OXTR, although it can also bind to the vasopressin unmodified oxytocin sequence was present in all placental mam- receptors (AVPR1a, AVPR1b, and AVPR2) with lower affinity mals. This study analyzed oxytocin (OXT) in 29 primate species and (11–13). Similar to other receptors that use G proteins as OXTR the oxytocin receptor ( ) in 21 of these species. We report transducer signals across the cell membranes, OXTR is com- here three novel OXT forms in the New World monkeys, as well posed of seven transmembrane (TM1–TM7), four extracellular as a more extensive distribution of a previously described variant (N-terminal tail-ECL3), and four intracellular (ICL1-C-terminal (Leu8Pro). -
8. Primate Evolution
8. Primate Evolution Jonathan M. G. Perry, Ph.D., The Johns Hopkins University School of Medicine Stephanie L. Canington, B.A., The Johns Hopkins University School of Medicine Learning Objectives • Understand the major trends in primate evolution from the origin of primates to the origin of our own species • Learn about primate adaptations and how they characterize major primate groups • Discuss the kinds of evidence that anthropologists use to find out how extinct primates are related to each other and to living primates • Recognize how the changing geography and climate of Earth have influenced where and when primates have thrived or gone extinct The first fifty million years of primate evolution was a series of adaptive radiations leading to the diversification of the earliest lemurs, monkeys, and apes. The primate story begins in the canopy and understory of conifer-dominated forests, with our small, furtive ancestors subsisting at night, beneath the notice of day-active dinosaurs. From the archaic plesiadapiforms (archaic primates) to the earliest groups of true primates (euprimates), the origin of our own order is characterized by the struggle for new food sources and microhabitats in the arboreal setting. Climate change forced major extinctions as the northern continents became increasingly dry, cold, and seasonal and as tropical rainforests gave way to deciduous forests, woodlands, and eventually grasslands. Lemurs, lorises, and tarsiers—once diverse groups containing many species—became rare, except for lemurs in Madagascar where there were no anthropoid competitors and perhaps few predators. Meanwhile, anthropoids (monkeys and apes) emerged in the Old World, then dispersed across parts of the northern hemisphere, Africa, and ultimately South America. -
Human-Nonhuman Primate Interconnections and Their Relevance to Anthropology
University of Nebraska - Lincoln DigitalCommons@University of Nebraska - Lincoln Ecological and Environmental Anthropology Wildlife Damage Management, Internet Center (University of Georgia) for November 2006 Human-Nonhuman Primate Interconnections and Their Relevance to Anthropology Agustin Fuentes University of Notre Dame Follow this and additional works at: https://digitalcommons.unl.edu/icwdmeea Part of the Environmental Sciences Commons Fuentes, Agustin, "Human-Nonhuman Primate Interconnections and Their Relevance to Anthropology" (2006). Ecological and Environmental Anthropology (University of Georgia). 1. https://digitalcommons.unl.edu/icwdmeea/1 This Article is brought to you for free and open access by the Wildlife Damage Management, Internet Center for at DigitalCommons@University of Nebraska - Lincoln. It has been accepted for inclusion in Ecological and Environmental Anthropology (University of Georgia) by an authorized administrator of DigitalCommons@University of Nebraska - Lincoln. Vol. 2, No. 2 Ecological and Environmental Anthropology 2006 Articles Human-Nonhuman Primate Interconnections and Their Relevance to Anthropology Agustín Fuentes The human-nonhuman primate interface is a core component in conservation and an emerging area of discourse across anthropology. There is a growing recognition of the relevance of long-term sympatry between human and nonhuman primates. Until recently these relationships received limited attention in the anthropological literature and in the primatological construction of models for the behavior and evolution of primate societies. Most socioecological investigations into primate groups and human populations do not incorporate their interactions (beyond predation or crop raiding), potential pathogen sharing, or the role of the anthropogenically impacted environment. Current relationships between humans and nonhuman primates are generally assumed to be rooted in conflict over land use and relatively recent, and thus have limited evolutionary and long term ecological impact. -
Primate Conservation
Primate Conservation Global evidence for the effects of interventions Jessica Junker, Hjalmar S. Kühl, Lisa Orth, Rebecca K. Smith, Silviu O. Petrovan and William J. Sutherland Synopses of Conservation Evidence ii © 2017 William J. Sutherland This work is licensed under a Creative Commons Attribution 4.0 International license (CC BY 4.0). This license allows you to share, copy, distribute and transmit the work; to adapt the work and to make commercial use of the work providing attribution is made to the authors (but not in any way that suggests that they endorse you or your use of the work). Attribution should include the following information: Junker, J., Kühl, H.S., Orth, L., Smith, R.K., Petrovan, S.O. and Sutherland, W.J. (2017) Primate conservation: Global evidence for the effects of interventions. University of Cambridge, UK Further details about CC BY licenses are available at https://creativecommons.org/licenses/by/4.0/ Cover image: Martha Robbins/MPI-EVAN Bwindi Impenetrable National Park, Uganda Digital material and resources associated with this synopsis are available at https://www.conservationevidence.com/ iii Contents About this book ............................................................................................................................. xiii 1. Threat: Residential and commercial development ............................ 1 Key messages ........................................................................................................................................ 1 1.1. Remove and relocate ‘problem’ -
Ancestral Facial Morphology of Old World Higher Primates (Anthropoidea/Catarrhini/Miocene/Cranium/Anatomy) BRENDA R
Proc. Natl. Acad. Sci. USA Vol. 88, pp. 5267-5271, June 1991 Evolution Ancestral facial morphology of Old World higher primates (Anthropoidea/Catarrhini/Miocene/cranium/anatomy) BRENDA R. BENEFIT* AND MONTE L. MCCROSSINt *Department of Anthropology, Southern Illinois University, Carbondale, IL 62901; and tDepartment of Anthropology, University of California, Berkeley, CA 94720 Communicated by F. Clark Howell, March 11, 1991 ABSTRACT Fossil remains of the cercopithecoid Victoia- (1, 5, 6). Contrasting craniofacial configurations of cercopithe- pithecus recently recovered from middle Miocene deposits of cines and great apes are, in consequence, held to be indepen- Maboko Island (Kenya) provide evidence ofthe cranial anatomy dently derived with regard to the ancestral catarrhine condition of Old World monkeys prior to the evolutionary divergence of (1, 5, 6). This reconstruction has formed the basis of influential the extant subfamilies Colobinae and Cercopithecinae. Victoria- cladistic assessments ofthe phylogenetic relationships between pithecus shares a suite ofcraniofacial features with the Oligocene extant and extinct catarrhines (1, 2). catarrhine Aegyptopithecus and early Miocene hominoid Afro- Reconstructions of the ancestral catarrhine morphotype pithecus. AU three genera manifest supraorbital costae, anteri- are based on commonalities of subordinate morphotypes for orly convergent temporal lines, the absence of a postglabellar Cercopithecoidea and Hominoidea (1, 5, 6). Broadly distrib- fossa, a moderate to long snout, great facial