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Evolution__3rd_Edition

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..<br />

Variable evolutionary rates upset<br />

distance methods<br />

Cladists prefer parsimony<br />

15.9.6 Distance, parsimony, and maximum likelihood methods are all<br />

used, but their popularity has changed over time<br />

Distance methods, parsimony, and maximum likelihood, in that order, require<br />

increasing amounts of data, and increasing computer power, in order for them to be<br />

used. Partly for this reason, the historic trend in phylogenetic research has been from<br />

using distance methods, which were used in the pioneering years of the late 1960s<br />

through to the early 1980s, to increasing use of parsimony, from the late 1970s to the<br />

1990s, to an increasing use of maximum likelihood through the 1990s and into the<br />

twenty-first century. Maximum likelihood is likely now the most widely used method<br />

of molecular phylogenetics.<br />

However, many biologists still use, and defend the use of, parsimony and distance<br />

methods. Some biologists think that molecules evolve in a basically clock-like manner,<br />

meaning that distance methods will usually give the right answer, and the sophistications<br />

of parsimony and maximum likelihood are unnecessary. But if some lineages<br />

evolve faster than others, distance methods misbehave a for much the same reason<br />

that simple phenetic similarity gives the wrong answer when comparing birds,<br />

crocodiles, and lizards (see Figure 15.6). Parsimony and maximum likelihood are less<br />

likely to go wrong.<br />

Parsimony has a particularly close relation with the methods of cladistics. The cladistic<br />

methods we looked at in the first part of this chapter are logically almost identical to<br />

the principle of parsimony. Parsimony counts evolutionary events, and each event generates<br />

a new derived character state. The use of homologies rather than homoplasies,<br />

and of derived rather than ancestral homologies, correspond to the principle of parsimony.<br />

Methods such as outgroup comparison (Section 15.6.1) are simple applications<br />

of parsimony. It is therefore no coincidence that the use of parsimony in phylogenetic<br />

inference, and of cladistics in systematics, rose hand-in-hand from about 1980<br />

onwards. (Chapter 16 considers cladistic systematics further.)<br />

The sheer quantity of DNA data that are available now, along with increased computer<br />

power, makes maximum likelihood (arguably) the most powerful method in<br />

modern biology. However, the use of maximum likelihood is still seriously limited by<br />

the power of computers (for reasons we return to in Section 15.11.2).<br />

15.10 Molecular phylogenetics in action<br />

CHAPTER 15 / The Reconstruction of Phylogeny 449<br />

15.10.1 Different molecules evolve at different rates and molecular<br />

evidence can be tuned to solve particular phylogenetic<br />

problems<br />

Different proteins, and stretches of DNA, evolve at different rates (Table 7.1, p. 161,<br />

and Table 7.6, p. 177), and they can be used like clocks with hands that revolve at<br />

different rates. If you use a rapidly evolving molecule for an ancient group, the<br />

molecule will have “turned over” many times during the phylogeny, and once multiple

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