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Evolution__3rd_Edition

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..<br />

Other factors are probably at work<br />

too<br />

Competition is strongest within a species. Each individual will, in many cases,<br />

encounter more members of its own species than of other species. Also, the members of<br />

its own species are more similar to it, exploiting more similar resources. One way to<br />

avoid competition is to become different from the competitors; hence there will be a<br />

force pushing similar competing types apart in evolution. Competition between similar<br />

individuals will make for the evolution of new adaptations in each that reduce the<br />

intensity of competition; divergence will thus result. Character displacement (Section<br />

13.6, p. 366) provides evidence that competition can cause divergence between closely<br />

related species. <strong>Evolution</strong>ary divergence is not inevitable, however. It depends on the<br />

contingencies of competition in particular cases. Provided that, on average, more similar<br />

individuals compete more closely, divergence is likely to result.<br />

Other factors probably also contribute to causing divergence. For instance, speciation<br />

is often allopatric and each pair of sister species becomes increasingly isolated<br />

over time by the Dobzhansky–Muller process (Section 14.4, p. 389). While the members<br />

of two populations interbreed, natural selection favors genetic changes that are<br />

advantageous in both populations. The two populations are kept relatively similar.<br />

Once the two populations have evolved apart and no longer interbreed, no force<br />

constrains the genetic changes that occur in one population also to be favorable in<br />

members of the other population. Incompatible genetic changes accumulate in the<br />

two populations (or species, as they are by this stage). The two gene pools have<br />

evolutionarily “escaped” from each another and are free to diverge further. Our<br />

modern genetic understanding of speciation has added to Darwin’s explanation for<br />

divergence.<br />

16.9 Conclusion<br />

CHAPTER 16 / Classification and <strong>Evolution</strong> 489<br />

Most biologists now accept that cladism is theoretically the best justified system of<br />

classification. It has a deep justification that phenetic and partly phenetic systems lack.<br />

Cladism is objective, and objective classifications are preferable to subjective ones. But<br />

despite cladism’s theoretical advantages, it can run into practical problems. The uncertainties<br />

of phylogenetic inference make cladistic classifications liable to frequent revision.<br />

True cladists are not very worried about that, and remark that all healthy theories<br />

are modified as new facts come in.<br />

Cladistic classification has become popular only recently. <strong>Evolution</strong>ary classification<br />

was the orthodox school from the “modern synthesis” of the 1930s (or even from<br />

Darwin’s time in the 1860s) until about 20 years ago. Numerical phenetics enjoyed a<br />

surge of support from the late 1950s to the early 1970s. Now, however, both schools<br />

have succumbed to cladistic criticism and have relatively few supporters. At all events,<br />

the most important point is to understand the arguments that have been used for and<br />

against each school: these arguments are of permanent importance in evolutionary<br />

biology.

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