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

Fig. 34. Alternative resolutions for three patterns <strong>of</strong> intergeneric <strong>relationships</strong> that exhibit nodal<br />

posterior probabilities ,0.95 in the Bayesian analysis <strong>of</strong> the concatenated five-gene dataset (see fig. 33). A,<br />

B, C, alternative <strong>relationships</strong> among Glironia, Hyladelphys + Didelphinae, <strong>and</strong> Caluromys +<br />

Caluromysiops; D, E, F, alternative <strong>relationships</strong> among Tlacuatzin, Marmosa, <strong>and</strong>Monodelphis; G, H,<br />

I, alternative <strong>relationships</strong> among Cryptonanus, Thylamys + Lestodelphys, <strong>and</strong>Gracilinanus. Black <strong>and</strong><br />

grey circles at nodes indicate posterior probabilities $0.95 or ,0.95, respectively. Branch lengths are<br />

shown at the same scale across all trees.<br />

(from 80% to 93%), as does the Bayesian<br />

posterior probability for placing the ingroup<br />

root between (Glironia (Caluromys + Caluromysiops))<br />

<strong>and</strong> other <strong>didelphid</strong>s (from 0.51 to<br />

0.87). Similarly, adding nonmolecular characters<br />

marginally improves the Bayesian<br />

posterior probability for Marmosa + Tlacuatzin<br />

(from 0.63 to 0.83).<br />

By contrast, including Chacodelphys in a<br />

combined-data parsimony analysis dramatically<br />

erodes bootstrap support for five<br />

intergeneric nodes (fig. 36). In fact, the strict<br />

consensus <strong>of</strong> 12 minimum-length trees (not<br />

shown) places Chacodelphys as the sister<br />

group <strong>of</strong> Monodelphis with weak (MPBS 5<br />

49%) support. Bayesian analysis, however,<br />

strongly supports the membership <strong>of</strong> Chacodelphys<br />

in a clade that also includes Gracilinanus,<br />

Cryptonanus, <strong>and</strong>Thylamys + Lestodelphys,<br />

<strong>and</strong> posterior probabilities for other<br />

nodes are substantially unaffected by taxon<br />

addition.<br />

Discussion<br />

Analyses <strong>of</strong> our combined dataset (excluding<br />

Chacodelphys; fig. 35) effectively summarize<br />

all <strong>of</strong> the shared <strong>phylogenetic</strong> signal that<br />

we have found to date in morphology,<br />

karyotypes, <strong>and</strong> five unlinked protein-coding<br />

nuclear genes. Additional support is provided<br />

by 16 parsimony-informative indels (figs. 29,<br />

30, 31) that were not coded as <strong>phylogenetic</strong><br />

characters but which optimize as synapomorphies<br />

on this topology. Lastly, this tree is<br />

congruent with the results <strong>of</strong> independent<br />

<strong>phylogenetic</strong> analyses based on sequence data<br />

from intron 1 <strong>of</strong> the nuclear transthyretin<br />

(TTR) gene <strong>and</strong> the mitochondrial 12S<br />

rDNA gene (Steiner et al., 2005). To the best

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