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phylogenetic relationships and classification of didelphid marsupials ...

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66 BULLETIN AMERICAN MUSEUM OF NATURAL HISTORY NO. 322<br />

Fig. 26. Scatterplot <strong>of</strong> percent GC content among <strong>didelphid</strong> sequences at first <strong>and</strong> second codon<br />

positions versus percent GC content at third codon positions for the five genes included in this study.<br />

<strong>didelphid</strong> terminal taxa. 21 To simplify comparisons<br />

<strong>of</strong> support values among the many<br />

(.1000) ingroup nodes recovered by these<br />

analyses, we restrict our attention to bootstrap<br />

frequencies (from MP <strong>and</strong> ML analyses)<br />

<strong>and</strong> Bayesian posterior probabilities, both <strong>of</strong><br />

which have respectable statistical pedigrees<br />

(Felsenstein, 1985; Efron et al., 1996; Huelsenbeck<br />

et al., 2002) despite their imperfect<br />

21 Marsupial interordinal <strong>relationships</strong> <strong>and</strong> <strong>relationships</strong><br />

among congeneric <strong>didelphid</strong> species will be treated in<br />

subsequent reports.<br />

relationship to type I error rates (Erixon et al.,<br />

2003; Alfaro <strong>and</strong> Holder, 2006).<br />

Analyses <strong>of</strong> Nonmolecular Data<br />

Despite the large amount <strong>of</strong> missing data<br />

from Chacodelphys (table 2), including this<br />

taxon in a parsimony analysis <strong>of</strong> our<br />

nonmolecular (morphological + karyotypic)<br />

characters resulted in fewer equally parsimonious<br />

trees (with a correspondingly betterresolved<br />

strict consensus) than we obtained<br />

from a parsimony analysis with Chacodelphys<br />

excluded (table 12). Among other notewor-

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