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Evolution__3rd_Edition

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..<br />

<strong>Evolution</strong>ary classification admits<br />

paraphyletic and monophyletic<br />

groups<br />

CHAPTER 16 / Classification and <strong>Evolution</strong> 485<br />

reasonable response to the problem of how to represent our phylogenetic knowledge in<br />

a formal classification. While only tens or hundreds of thousands of species had been<br />

named, and phylogenetics was a backwater of biological research, Hennig’s cladistic<br />

principles posed little challenge to the Linnaean system of ranks. Now we know about<br />

millions of species, and molecular systematics is a major research program. Some<br />

adjustments to the Linnaean system may yet be needed to accommodate our expanding<br />

phylogenetic knowledge, but meanwhile, it remains useful to classify biological species<br />

into the Linnaean higher taxa. But decisions about which levels of the Linnaean hierarchy<br />

to apply to which nodes in a phylogeny are arbitrary and subjective.<br />

16.7 <strong>Evolution</strong>ary classification is a synthesis of phenetic<br />

and phylogenetic principles<br />

Finally, we should look at evolutionary classification. <strong>Evolution</strong>ary classification<br />

incorporates both phenetic and phylogenetic elements, and both paraphyletic and<br />

monophyletic groups. In terms of the kinds of taxonomic groups (see Figure 16.4),<br />

evolutionary classification recognizes paraphyletic and monophyletic but not polyphyletic<br />

groups. In terms of the kinds of characters used to infer phylogeny (see<br />

Figure 16.3), it forms groups by homologies rather than homoplasies, but does not distinguish<br />

ancestral from derived homologies. Referring back to Figure 16.1, evolutionary<br />

classification picks the phenetic classification in the reptilian case (Figure 16.1c) but<br />

the phylogenetic where there is convergence (Figure 16.1b).<br />

How can evolutionary taxonomy be justified? The evolutionary school predates<br />

both numerical phenetics and cladism and the main original discussions of the school<br />

therefore did not meet the phenetic and cladistic arguments head on. Moreover, no<br />

complete modern evolutionary taxonomic defense against numerical and cladistic<br />

taxonomy exists. As such, the school differs from the other two, which were conceived<br />

partly in opposition to evolutionary taxonomy and made their objections to it clear.<br />

Nevertheless, a case can be made.<br />

<strong>Evolution</strong>ary taxonomists disagree with phenetic classification for much the same<br />

reasons we discussed above, though they express the argument differently. They<br />

criticized phenetic systems for being idealistic, that is for supposing that a phenetic<br />

classification represents some “ideal” phenetic relationship between species. The<br />

ideal relationship would be some “idea” or “plan” in nature. An example is the pre-<br />

Darwinian theory that classifications represent the thoughts of God. An idealist would<br />

then aim to classify species according to an idea that exists in the mind of God. That<br />

idea, arguably, manifests itself in (and is inferrable from) living nature. It is difficult for<br />

a modern scientist to make much sense of these old arguments, but “divine” taxonomy<br />

at least provides a concrete example of what idealism means. Other versions of idealism<br />

supposed that it was possible to deduce the existence of fundamental forms or plans of<br />

nature from a purely scientific analysis of species’ morphology. 1<br />

1 Section 13.5, p. 363, about “typological thinking,” is concerned with much the same point. Idealism is an<br />

example of typological thinking.

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