| Preface |
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Introduction to biogeography |
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1 | (14) |
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11 | (1) |
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12 | (1) |
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13 | (2) |
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A history of biogeography |
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15 | (30) |
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15 | (3) |
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Ecological versus historical biogeography, and plants versus animals |
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18 | (1) |
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Biogeography and Creation |
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19 | (2) |
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Distribution of life today |
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21 | (2) |
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Evolution--a flawed and dangerous idea! |
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23 | (1) |
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24 | (1) |
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World maps: the biogeographical regions of plants and animals |
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25 | (3) |
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28 | (3) |
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The origins of modern historical biogeography |
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31 | (5) |
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The development of ecological biogeography |
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36 | (1) |
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37 | (2) |
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39 | (2) |
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41 | (2) |
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43 | (1) |
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43 | (1) |
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43 | (2) |
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45 | (28) |
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How many species are there? |
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46 | (6) |
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52 | (8) |
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60 | (2) |
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62 | (6) |
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68 | (1) |
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68 | (2) |
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70 | (1) |
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70 | (1) |
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70 | (3) |
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73 | (46) |
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74 | (1) |
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75 | (2) |
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A successful family: the daisies (Asteraceae) |
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77 | (3) |
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80 | (3) |
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Magnolias: evolutionary relicts |
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83 | (2) |
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85 | (4) |
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89 | (1) |
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90 | (1) |
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91 | (5) |
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96 | (3) |
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99 | (2) |
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101 | (6) |
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107 | (3) |
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110 | (2) |
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112 | (4) |
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116 | (1) |
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116 | (1) |
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116 | (3) |
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Communities and ecosystems |
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119 | (24) |
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120 | (2) |
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122 | (3) |
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Ecosystems and biodiversity |
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125 | (3) |
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Biotic assemblages on a global scale |
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128 | (4) |
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132 | (6) |
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Modelling biomes and climate |
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138 | (2) |
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Biomes in a changing world |
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140 | (1) |
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141 | (1) |
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141 | (1) |
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142 | (1) |
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143 | (22) |
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144 | (1) |
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Darwin's explanation and Darwin's finches |
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145 | (4) |
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Controlling forces within the organism |
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149 | (1) |
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From populations to species |
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150 | (2) |
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152 | (1) |
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Barriers to interbreeding |
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153 | (2) |
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155 | (1) |
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The `theory' of natural selection |
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156 | (2) |
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Controversies and evolutionary theory |
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158 | (2) |
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Evolution and the human race(s) |
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160 | (2) |
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162 | (1) |
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162 | (1) |
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162 | (3) |
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Life, death and evolution on islands |
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165 | (36) |
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166 | (2) |
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Getting there: problems of access |
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168 | (2) |
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Dying there: problems of survival |
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170 | (2) |
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Integrating the data: the Theory of Island Biogeography |
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172 | (2) |
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Second thoughts about the Theory |
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174 | (2) |
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The Theory of Island Biogeography and the design of nature reserves |
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176 | (3) |
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Starting afresh: the story of Rakata |
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179 | (7) |
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180 | (1) |
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181 | (5) |
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Evolving there: opportunities for adaptive radiation |
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186 | (4) |
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190 | (7) |
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192 | (1) |
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Evolutionary radiations within the Hawaiian Islands |
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193 | (4) |
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197 | (1) |
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197 | (1) |
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197 | (4) |
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201 | (24) |
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202 | (3) |
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Evidence for past geographies |
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205 | (1) |
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Early land life on the moving continents |
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206 | (3) |
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209 | (5) |
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Rise of the flowering plants |
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214 | (2) |
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Late Cretaceous and Cenozoic changes in geography, ocean currents and climate |
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216 | (3) |
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Late Cretaceous and Cenozoic floral changes |
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219 | (3) |
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222 | (1) |
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222 | (1) |
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222 | (3) |
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The geography of life today |
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225 | (36) |
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Mammals: the final patterns |
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227 | (6) |
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The distribution of flowering plants today |
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233 | (2) |
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Mammalian versus flowering plant geography: comparisons and contrasts |
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235 | (2) |
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The Old World tropics: Africa, India and South-East Asia |
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237 | (6) |
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238 | (2) |
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240 | (1) |
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241 | (1) |
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India and South-East Asia |
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242 | (1) |
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243 | (2) |
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245 | (2) |
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247 | (4) |
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251 | (4) |
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Late Cretaceous/Early Cenozoic |
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251 | (1) |
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251 | (1) |
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Late Cenozoic/Pleistocene |
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252 | (3) |
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The Northern Hemisphere: Holarctic mammals and Boreal plants |
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255 | (3) |
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258 | (1) |
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258 | (1) |
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258 | (3) |
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261 | (36) |
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262 | (2) |
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Interglacials and interstadials |
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264 | (2) |
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Biological changes in the Pleistocene |
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266 | (2) |
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268 | (6) |
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274 | (5) |
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The current interglacial: a false start |
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279 | (3) |
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282 | (5) |
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287 | (1) |
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288 | (2) |
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290 | (1) |
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291 | (2) |
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293 | (1) |
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294 | (1) |
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294 | (1) |
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295 | (2) |
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297 | (22) |
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297 | (6) |
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Modern humans and the megafaunal extinctions |
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303 | (1) |
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Domestication and agriculture |
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304 | (7) |
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The biogeography of human parasitic diseases |
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311 | (3) |
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Environmental impact of early human cultures |
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314 | (1) |
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315 | (1) |
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316 | (1) |
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316 | (3) |
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Drawing lines in the water |
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319 | (34) |
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Zones in the ocean and upon the sea floor |
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323 | (2) |
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Basic biogeography of the seas |
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325 | (1) |
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326 | (11) |
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Dynamics of the ocean basins |
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326 | (3) |
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Patterns of life in the ocean waters: biomes and provinces within the oceans |
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329 | (4) |
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Patterns of life on the ocean floor |
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333 | (3) |
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Biogeography of hydrothermal vent faunas |
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336 | (1) |
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337 | (13) |
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Faunal breaks within the shelf faunas |
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339 | (2) |
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Coastal faunas of islands |
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341 | (1) |
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Trans-oceanic links and barriers between shelf faunas |
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341 | (2) |
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Latitudinal patterns in the shelf faunas |
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343 | (1) |
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344 | (6) |
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350 | (1) |
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350 | (1) |
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350 | (3) |
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Interpreting the past: I. Molecular and isotopic biogeography |
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353 | (18) |
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354 | (2) |
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DNA, RNA, enzymes and phylogeny |
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356 | (2) |
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358 | (1) |
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Molecular evolution and bird biogeography |
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359 | (3) |
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Human biogeography and molecular methods |
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362 | (1) |
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Population crashes, bottlenecks and catastrophes |
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363 | (2) |
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365 | (2) |
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Isotopes in biogeochemical cycles |
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367 | (1) |
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368 | (1) |
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369 | (1) |
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369 | (1) |
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369 | (2) |
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Interpreting the past: II. Principles and practice |
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371 | (20) |
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The great divide: dispersal versus vicariance |
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371 | (3) |
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Centres of dispersal and centres of origin |
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374 | (1) |
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Current methods of biogeographical analysis |
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374 | (2) |
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Phylogenetic biogeography |
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376 | (1) |
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377 | (2) |
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379 | (1) |
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380 | (1) |
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Parsimony analysis of endemicity |
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381 | (1) |
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Endemicity and Pleistocene problems |
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382 | (3) |
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The `New Zealand school' of panbiogeography |
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385 | (2) |
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387 | (1) |
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388 | (1) |
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388 | (1) |
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389 | (2) |
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391 | (26) |
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392 | (3) |
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395 | (4) |
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Nitrogen and sulphur overload |
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399 | (2) |
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401 | (1) |
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Biogeographical consequences of global change |
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402 | (4) |
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Population declines and extinctions |
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406 | (3) |
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Changing communities and biomes |
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409 | (1) |
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Where do we go from here? |
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410 | (3) |
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413 | (1) |
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413 | (1) |
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413 | (4) |
| Index |
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417 | |