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Evolution__3rd_Edition

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Full Contents xv<br />

14.2 A newly evolving species could theoretically have an allopatric,<br />

parapatric, or sympatric geographic relation with its ancestor 382<br />

14.3 Reproductive isolation can evolve as a by-product of divergence<br />

in allopatric populations 383<br />

14.3.1 Laboratory experiments illustrate how separately evolving<br />

populations of a species tend incidentally to evolve<br />

reproductive isolation 384<br />

14.3.2 Prezygotic isolation evolves because it is genetically correlated<br />

with the characters undergoing divergence 386<br />

14.3.3 Reproductive isolation is often observed when members of<br />

geographically distant populations are crossed 387<br />

14.3.4 Speciation as a by-product of divergence is well documented 389<br />

14.4 The Dobzhansky–Muller theory of postzygotic isolation 389<br />

14.4.1 The Dobzhansky–Muller theory is a genetic theory of<br />

postzygotic isolation, explaining it by interactions among<br />

many gene loci 389<br />

14.4.2 The Dobzhansky–Muller theory is supported by extensive<br />

genetic evidence 391<br />

14.4.3 The Dobzhansky–Muller theory has broad biological<br />

plausibility 392<br />

14.4.4 The Dobzhansky–Muller theory solves a general problem<br />

of “valley crossing” during speciation 394<br />

14.4.5 Postzygotic isolation may have ecological as well as genetic<br />

causes 395<br />

14.4.6 Postzygotic isolation usually follows Haldane’s rule 396<br />

14.5 An interim conclusion: two solid generalizations about speciation 399<br />

14.6 Reinforcement 399<br />

14.6.1 Reproductive isolation may be reinforced by natural selection 399<br />

14.6.2 Preconditions for reinforcement may be short lived 401<br />

14.6.3 Empirical tests of reinforcement are inconclusive or fail to<br />

support the theory 402<br />

14.7 Some plant species have originated by hybridization 405<br />

14.8 Speciation may occur in non-allopatric populations, either<br />

parapatrically or sympatrically 408<br />

14.9 Parapatric speciation 409<br />

14.9.1 Parapatric speciation begins with the evolution of a<br />

stepped cline 409<br />

14.9.2 Evidence for the theory of parapatric speciation is<br />

relatively weak 411<br />

14.10 Sympatric speciation 411<br />

14.10.1 Sympatric speciation is theoretically possible 411<br />

14.10.2 Phytophagous insects may split sympatrically by host shifts 412<br />

14.10.3 Phylogenies can be used to test whether speciation has been<br />

sympatric or allopatric 413<br />

14.11 The influence of sexual selection in speciation is one current trend<br />

in research 413

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