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

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S. Meiri et al.<br />

Insular mean SVL (log 10 scale)<br />

Insular mean mass (log 10 scale)<br />

Birds<br />

(a) (b)<br />

Continental mean SVL (log 10 scale)<br />

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

Of 8069 bird species in our dataset, 1347 are insular endemics<br />

(we have maximum mass data <strong>for</strong> all, and <strong>for</strong> 7552, including<br />

1268 insular endemic species, we have data on mean <strong>size</strong>;<br />

Appendix S1b). In 90 out of 223 avian genera the largest<br />

member of the clade is an insular endemic. This is significantly<br />

more than expected under our randomizations (median<br />

expected = 71; P < 0.01, Table 1). However, at the family<br />

and order levels (see <strong>size</strong> frequency histograms in Appendix<br />

S3b) the largest member of a clade is no more often an<br />

insular endemic than expected at random. The frequency with<br />

which the smallest member of a clade is an insular endemic<br />

does not depart from the null expectation <strong>for</strong> any taxonomic<br />

level. Moreover, when we repeated the analysis at the genus<br />

level using the maximum rather than mean <strong>body</strong> <strong>size</strong> (data are<br />

the maximum reported <strong>for</strong> a species in Dunning, 2008),<br />

neither the frequency of gigantism nor dwarfism departed<br />

from the null expectation (67 observed insular maxima across<br />

219 genera, median expected = 71, P = 0.53).<br />

There was no <strong>evidence</strong> <strong>for</strong> the island rule at the genus and<br />

family level in birds, with slopes equal to 1.00 and 0.98,<br />

Continental mean mass (log 10 scale)<br />

respectively (Fig. 3a,b). The slope at the order level, however,<br />

was significantly shallower than 1 (SMA slope = 0.76, 95%<br />

CI = 0.66–0.88, r = )0.70, P < 0.01; P randomization < 0.01;<br />

Fig. 3c), even when ratites are excluded (SMA slope = 0.78,<br />

95% CI = 0.64–0.95, r = )0.56, P < 0.05; Prandomization <<br />

0.05).<br />

Mammals<br />

Figure 2 Standardized major axis regression<br />

of mean <strong>body</strong> <strong>size</strong> [log 10-trans<strong>for</strong>med<br />

snout–vent length (SVL) in mm] on islands<br />

versus continents <strong>for</strong> species in lizard genera<br />

(a) and families (b). The dashed line has a<br />

slope of 1 and an intercept of 0. The solid line<br />

represents the standardized major axis<br />

regression slope estimate.<br />

Figure 3 Standardized major axis regression of mean <strong>body</strong> <strong>size</strong> (log 10-trans<strong>for</strong>med mass, in g) on islands versus continents <strong>for</strong> species in<br />

bird genera (a), families (b) and orders (c). The dashed line has a slope of 1 and an intercept of 0. The solid line represents the standardized<br />

major axis regression slope estimate.<br />

Of 3961 extant mammal species, 670 are insular endemics (778<br />

of 4213 when extinct species are included). The frequency of<br />

insular endemics that are either the largest or smallest<br />

members of their clades does not depart from the null<br />

expectation derived by randomization at any taxonomic level,<br />

either including or excluding extinct taxa (Table 1, Appendix<br />

S3c).<br />

In agreement with the results from randomizations, the<br />

frequency of gigantism and dwarfism tended not to exceed the<br />

null expectation generated under a single-rate Brownian model<br />

on the mammalian phylogeny. This was true <strong>for</strong> all taxonomic<br />

levels, both including and excluding extinct species, except <strong>for</strong><br />

6 Journal of Biogeography<br />

ª 2010 Blackwell Publishing Ltd

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