| Preface |
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xi | |
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18 | (54) |
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The Emergence of the Genetic Paradigm |
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19 | (3) |
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Mathematical, Material, and Computational Genetics |
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22 | (3) |
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The Power and Pervasiveness of Statistics |
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25 | (2) |
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R.A. Fisher: Statistics, Genetics, and Eugenics |
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27 | (3) |
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30 | (3) |
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33 | (31) |
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Questioning European Origins |
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34 | (3) |
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Evolution within Africa; Migrations Out of Africa |
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37 | (6) |
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Our Ancestral Mother and Father |
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43 | (9) |
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52 | (4) |
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56 | (8) |
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64 | (3) |
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67 | (5) |
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3 The Mind, the Lab, and the Field: Three Kinds of Populations |
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72 | (26) |
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Three Kinds of Populations |
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75 | (10) |
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Fisher on Theoretical Populations |
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76 | (3) |
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Park on Laboratory Populations |
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79 | (3) |
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Lack on Natural Populations |
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82 | (3) |
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Distinguishing Population Types |
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85 | (10) |
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"Effective Population Size" as a Barrier: Distinguishing Theoretical from Natural Populations |
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86 | (4) |
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The Danger of Conflation: Theoretical and Natural Populations in Structure Analyses |
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90 | (5) |
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Assumption Archaeology and Population Pluralism |
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95 | (3) |
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98 | (32) |
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The Meanings of Metrics and Measures: Realism or Constructivism? |
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101 | (2) |
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Three Metrics and Measures of Genetic Variation |
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103 | (9) |
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103 | (2) |
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105 | (4) |
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109 | (1) |
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Contrasting (Genetic) Diversity, Heterozygosity, and Differentiation |
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110 | (2) |
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Theoretical and Disciplinary Homes |
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112 | (14) |
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114 | (2) |
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116 | (2) |
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Lewontin (1972): Taxonomy Meets Conservation Biology |
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118 | (4) |
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122 | (4) |
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Homo sapiens: A Special Case |
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126 | (4) |
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5 Models and Methodologies |
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130 | (34) |
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A Tale of Two Methodologies |
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134 | (15) |
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138 | (6) |
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144 | (4) |
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Mutual Methodological Consistency |
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148 | (1) |
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When Maps Become the World |
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149 | (13) |
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150 | (7) |
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157 | (2) |
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159 | (1) |
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Statistic--Parameter Reification |
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160 | (2) |
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Whither the Two Methodologies? |
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162 | (2) |
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6 Six Patterns of Human Genomic Variation |
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164 | (26) |
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166 | (23) |
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1 There Is Low Intraspecies Genomic Variation |
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167 | (1) |
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2 There Are Small, But Often Critical, Interspecies Differences |
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168 | (3) |
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3 Of All Continental Regions, Africa Has The Oldest - And Thus The Richest And Most Encompassing -- Human Genomic Variation |
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171 | (5) |
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4 Most Genetic Variation Is Among Individuals Within Populations, Not Across Populations Within Continental Regions, Nor Across Different Continental Regions (Lewontin's Distribution) |
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176 | (9) |
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5 Despite Lewontin's Distribution, Clustering Populations And Classifying Individuals Is Possible |
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185 | (2) |
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6 Genomic Heterozygosity Of Populations Decreases With Increasing Distance From Africa, Along Human Migration Routes |
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187 | (2) |
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189 | (1) |
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190 | (36) |
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Natural Selection: Distinctions and Complementarity |
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192 | (7) |
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The Genomic Signature of Natural Selection |
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199 | (2) |
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Determining the Legible Signature of Selection |
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201 | (13) |
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Case Study: Freediving Physiology |
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214 | (9) |
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217 | (1) |
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218 | (1) |
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219 | (2) |
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221 | (1) |
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221 | (1) |
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222 | (1) |
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223 | (3) |
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8 Intelligence, Female Orgasm, and Future Discovery |
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226 | (36) |
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Gene versus Environment in Disease |
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228 | (9) |
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Intelligence, Female Orgasm, and Future Discovery |
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237 | (22) |
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238 | (5) |
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243 | (16) |
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The Distinction Between Gene and Environment, and the Adaptationist Paradigm |
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259 | (3) |
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262 | (22) |
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Philosophers of Race Speak |
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264 | (3) |
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The Reality and Reification of Race |
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267 | (3) |
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Lewontin's Distribution and "Lewontin's Fallacy": When the Single Shannon Just Isn't Enough |
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270 | (5) |
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The Song Remains the Same |
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275 | (4) |
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Political Consequences and Possible Futures |
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279 | (4) |
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283 | (1) |
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10 The Conscious Universe: Genes in Complex Systems |
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284 | (30) |
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Clockwork, Soup, and Consciousness |
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286 | (2) |
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Chance, Law, and the Limits of Total Explanation |
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288 | (7) |
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Statistics in a Conscious Universe |
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295 | (9) |
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Philosophies of Causation |
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304 | (1) |
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305 | (2) |
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An Invitation to the Reader |
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307 | (1) |
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308 | (3) |
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311 | (3) |
| References |
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314 | (44) |
| Index |
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358 | |