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Slaying dragons: limited evidence for unusual body size evolution ...

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Body <strong>size</strong> of island taxa<br />

Body <strong>size</strong> of island taxa<br />

No island rule, no insular <strong>size</strong> extremes<br />

the more dramatic cases of insular <strong>size</strong> <strong>evolution</strong>, where<br />

changes are drastic enough to merit different specific status.<br />

Thus intra-specific studies will omit from consideration, <strong>for</strong><br />

example, Elephas falconeri, which evolved to just 1% of the<br />

mass of its mainland ancestor (Roth, 1992), and even studies<br />

conducted on species within genera will miss members of<br />

insular endemic genera such as the c. 100 kg insular rodent<br />

Amblyrhiza inundata (Biknevicius et al., 1993) and the largest<br />

gecko, Hoplodactylus delcourti (Russell & Bauer, 1986).<br />

Here we examine, in a purely inter-specific fashion, whether:<br />

(1) species with extreme <strong>body</strong> <strong>size</strong>s (i.e. the largest and smallest<br />

species) in a subclade are more often insular endemics than<br />

expected by chance given the number of insular endemics in<br />

the subclade; and (2) if there is <strong>evidence</strong> <strong>for</strong> a pattern<br />

consistent with the island rule above the species level using<br />

mean <strong>size</strong>s of insular and mainland species within clades.<br />

No island rule, insular <strong>size</strong> extremes<br />

(a) (b) (c)<br />

Body <strong>size</strong> of mainland taxa<br />

Island rule, insular <strong>size</strong> extremes No island rule, insular <strong>size</strong> extremes<br />

(d) (e) (f)<br />

Body <strong>size</strong> of mainland taxa<br />

We use nearly complete datasets of species <strong>body</strong> <strong>size</strong>s of<br />

mammals, birds and lizards. For mammals (only) a comprehensive<br />

species-level phylogeny and an excellent late Pleistocene<br />

fossil record exist. This meant that we were also able to<br />

use a sister-clade comparison, and include data <strong>for</strong> species<br />

that went extinct since the end of the last glacial, which<br />

include some of the most pronounced cases of insular <strong>size</strong><br />

<strong>evolution</strong>.<br />

MATERIALS AND METHODS<br />

Data<br />

Island vertebrates and <strong>body</strong> <strong>size</strong> extremes<br />

Island rule, no insular <strong>size</strong> extremes<br />

Reversed island rule, insular <strong>size</strong> extremes<br />

Figure 1 Schemes showing possible ways in which patterns of <strong>body</strong> <strong>size</strong> on islands and mainland within taxa (<strong>size</strong> extremes or average<br />

<strong>size</strong>s) can combine to produce patterns of <strong>body</strong> <strong>size</strong> across taxa (slope 1). x-axis, mainland <strong>body</strong> <strong>size</strong>; y-axis,<br />

island <strong>body</strong> <strong>size</strong>; dashed line, a line with an intercept of 0 and a slope of 1; solid line, slope returned by standardized major axis regression<br />

(can mask the dashed line). The <strong>body</strong> <strong>size</strong> frequency distributions depict insular (top) and mainland members of a clade (bottom). The<br />

mainland mean <strong>size</strong> is indicated by the vertical, dashed line. (a) The null distribution. No insular <strong>size</strong> extremes, no island rule (slope of 1,<br />

similar insular and mainland <strong>size</strong> ranges). (b) There are <strong>size</strong> extremes because island taxa have wider <strong>size</strong> distributions, but no island<br />

rule because mean <strong>size</strong>s are similar (slope of 1). (c) The island rule holds (small animals evolve larger <strong>size</strong> and large ones dwarf, slope

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