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Preface |
page xv |
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Acknowledgments |
xvii |
| 1. |
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Introduction |
1 |
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The primate order |
1 |
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Ape and monkey bias |
11 |
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Evolution before natural selection |
13 |
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1858–1859: The advent of natural selection theory |
15 |
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Essentialism versus population-thinking |
20 |
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1863: Thomas Henry Huxley and the place of humans in nature |
22 |
| 2. |
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A brief history of primatology and human evolution |
26 |
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Introduction |
26 |
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Antiquity and the Middle Ages |
30 |
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The Renaissance to the late eighteenth century |
32 |
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The nineteenth century |
36 |
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The early twentieth century |
37 |
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The “new” physical anthropology |
43 |
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1959 – annus mirabilis |
44 |
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The baboon renaissance |
50 |
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Sociobiology and behavioral ecology |
53 |
| 3. |
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The catarrhine fossil record |
56 |
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The geological time scale |
56 |
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Major features of primate evolution |
56 |
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The shape and pattern of primate evolution |
57 |
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The early catarrhine primates |
62 |
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Hominoid systematics |
64 |
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The Miocene hominoid radiation |
65 |
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Community structure and competition between primate species |
70 |
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The end of the hominoid radiation and the rise of the cercopithecoids |
73 |
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Climate change in the late Miocene and the first hominids |
76 |
| 4. |
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Primate speciation and extinction |
81 |
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Primate speciation and extinction in the geological past |
81 |
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Speciation in modern primates |
86 |
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Extinction in modern primates |
94 |
| 5. |
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Anatomical primatology |
107 |
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Introduction |
107 |
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Phylogeny and cladistic methodology |
107 |
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Adaptation and the “adaptationist program” |
115 |
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Studying adaptation |
117 |
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The functional morphology of fossil species |
119 |
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Ontogeny and anatomical genomics |
124 |
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Phenotypic variability |
126 |
| 6. |
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Captive studies of non-human primates |
128 |
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Introduction |
128 |
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The influence of captivity on behavior |
128 |
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Harry Harlow’s research |
130 |
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An inventory of abnormal captive behaviors |
130 |
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Biomedical primatology |
137 |
| 7. |
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What can non-human primate anatomy, physiology, and development reveal about human evolution? |
141 |
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The catarrhine substrate |
141 |
| 8. |
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Natural history intelligence and human evolution |
146 |
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Introduction |
146 |
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Ideas on the origins of hominid intelligence |
150 |
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Hominid attention to natural history |
155 |
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Animal behavior and artificial intelligence |
157 |
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Natural history intelligence |
159 |
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Problems with the social cognition model |
163 |
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Further primatological evidence against social cognition as a generator of intelligence |
167 |
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Brain mechanisms underlying natural history intelligence |
171 |
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Other tests of the social cognition theory |
179 |
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Natural history intelligence over the course of human evolution |
180 |
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Conclusions |
182 |
| 9. |
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Why be social? – the advantages and disadvantages of social life |
185 |
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Why be social? |
185 |
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How to become social |
188 |
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Explanations of primate social complexity |
194 |
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What is the catarrhine substrate for sociality? |
194 |
| 10. |
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Evolution and behavior |
196 |
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Proximate and ultimate factors in behavioral evolution |
196 |
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Factors limiting population size |
197 |
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Diet and foraging behavior |
198 |
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Cultural traditions |
199 |
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Phylogenetic inertia and phylogenetic constraint |
201 |
| 11. |
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The implications of body size for evolutionary ecology |
203 |
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Introduction |
203 |
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Measuring body size in fossil species |
208 |
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Body size and paleocommunity reconstructions |
209 |
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Body size and behavior |
213 |
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The all-too-familiar use of sexual dimorphism to infer sociality in fossil species |
215 |
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Reversible body size changes in individuals |
218 |
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Size and shape changes: adaptation and plasticity |
220 |
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Population-level differences in body size |
231 |
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What can be inferred from body size in fossil species? |
236 |
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The sweating response, body shape, and heat adaptation |
239 |
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The evolution of body size in primates |
245 |
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Conclusions |
248 |
| 12. |
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The nature of the fossil record |
252 |
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Does the fossil record faithfully record past events? |
252 |
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Decimation and recovery from extinction |
259 |
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Rates of evolutionary change |
262 |
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Time-averaging |
265 |
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Taphonomy and experimental studies |
266 |
| 13. |
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The bipedal breakthrough |
271 |
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Introduction |
271 |
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Ape models for bipedal origins |
271 |
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Behavior and morphology |
276 |
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Bipedal efficiency |
277 |
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Paleoenvironment |
280 |
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Bipedal origins |
280 |
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Lessons from Oreopithecus |
288 |
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A mixture of morphologies |
290 |
| 14. |
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The hominid radiation |
292 |
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The earliest hominids |
292 |
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Plio-Pleistocene hominids |
293 |
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The single-species hypothesis |
293 |
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Sympatry and multiple hominid niches |
298 |
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Sexual dimorphism and niche structure |
303 |
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The origin of genus Homo |
305 |
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Hominid dispersion from sub-Saharan Africa |
306 |
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Asian ape-men: Early ideas about hominid origins in Asia |
306 |
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The origins of anatomically modern humans |
308 |
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Genetic variation in modern humans |
310 |
| 15. |
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Modeling human evolution |
311 |
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Baboon models |
311 |
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Referential and conceptual models |
313 |
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A “composite mammal” model |
314 |
| 16. |
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Archeological evidence and models of human evolution |
317 |
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Human antiquity |
317 |
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Recognition that the archeological record is not coeval with the human paleontological record |
321 |
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Bone modification and inferences of hominid behavior |
329 |
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Climatic events and the archeological record |
331 |
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“Man the Hunter” and the new physical anthropology |
333 |
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Food, food-sharing, and division of labor |
336 |
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Pair-bonding |
340 |
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Taphonomy and the nature of “sites” |
343 |
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The hominization process |
344 |
| 17. |
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What does evolutionary anthropology reveal about human evolution? |
351 |
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Phenotypic change and “contemporary evolution” |
351 |
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Body size and shape changes |
353 |
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What factors are responsible for the origin of generalized species? |
361 |
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Tool behavior and technology |
366 |
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Language |
369 |
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Early hominid sociality |
371 |
| 18. |
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Final thoughts on primate and human evolution |
382 |
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Speciation, extinction, and other evolutionary processes |
382 |
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Terrestrial life and bipedality |
384 |
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Tool behavior |
385 |
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Intelligence |
386 |
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Complex sociality |
387 |
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References |
389 |
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Index |
452 |