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2009 VOSS AND JANSA: DIDELPHID MARSUPIALS 67<br />

TABLE 11<br />

Results <strong>of</strong> Maximum-likelihood Model Fitting with Single-gene Datasets<br />

BRCA1 vWF IRBP DMP1 RAG1 a<br />

Model<br />

Parameter estimates:<br />

GTR + C TVMef + I + C GTR + I + C GTR + C GTR + I + C<br />

pA 0.37 0.25 0.25 0.37 0.31<br />

pC 0.19 0.25 0.26 0.18 0.23<br />

pG 0.21 0.25 0.27 0.26 0.24<br />

pT 0.23 0.25 0.22 0.18 0.22<br />

rAC 0.91 2.03 1.96 1.12 3.03<br />

rAG 4.75 7.01 5.88 2.64 4.59<br />

rAT 0.76 1.26 1.46 0.39 0.77<br />

rCG 1.05 1.07 1.13 0.77 1.73<br />

rCT 5.52 7.01 7.43 6.74 7.22<br />

a 1.48 0.83 0.81 0.69 0.41<br />

pinv 0.00 0.19 0.32 0.00 0.52<br />

Ln-likelihood b<br />

215078.42 26648.62 26817.82 25943.66 26343.58<br />

a First <strong>and</strong> second codon positions only.<br />

b Of best tree.<br />

thy features <strong>of</strong> this topology (fig. 27), <strong>didelphid</strong><br />

monophyly is only weakly supported, as<br />

are most patterns <strong>of</strong> intergeneric <strong>relationships</strong>.<br />

In fact, only six genera <strong>and</strong> intergeneric<br />

clades are strongly supported (with bootstrap<br />

values .75%) by parsimony analysis <strong>of</strong> these<br />

data: (1) a group containing Lestodelphys <strong>and</strong><br />

Thylamys; (2) a group that includes Caluromys<br />

<strong>and</strong> Caluromysiops; (3) the genus<br />

Didelphis; (4) a group that includes Lutreolina,<br />

Phil<strong>and</strong>er, <strong>and</strong> Didelphis; (5) a group<br />

that includes the latter three genera plus<br />

Chironectes; <strong>and</strong> (6) the genus Monodelphis.<br />

However, several other groups (e.g., the<br />

genus Thylamys, the genus Marmosops, the<br />

genus Caluromys, the genus Phil<strong>and</strong>er, <strong>and</strong><br />

Phil<strong>and</strong>er + Didelphis) receive moderate<br />

bootstrap support.<br />

Bayesian analysis <strong>of</strong> these nonmolecular<br />

data (implementing the Mkv model <strong>of</strong> Lewis,<br />

2001) provides strong support (posterior<br />

probabilities .95%) for most <strong>of</strong> the same<br />

clades that are strongly supported by parsimony,<br />

with the notable exception <strong>of</strong> (4)<br />

among those listed above. In addition, there<br />

is strong Bayesian support for the monophy-<br />

TABLE 12<br />

Results <strong>of</strong> Parsimony Analyses <strong>of</strong> Datasets with Nonmolecular Characters<br />

Nonmolecular data a<br />

Combined data b<br />

w/ Chacodelphys w/o Chacodelphys w/ Chacodelphys w/o Chacodelphys<br />

Ingroup taxa 44 43 44 43<br />

Outgroup taxa 7 7 7 7<br />

Total characters 129 129 7449 7449<br />

Informative characters 114 114 2073 2073<br />

Minimum-length trees 1068 21,803 12 12<br />

Length <strong>of</strong> best trees 362 356 5960 5954<br />

Consistency Index 0.508 0.517 0.638 0.639<br />

Retention Index 0.788 0.793 0.777 0.777<br />

Resolved nodes (%) c<br />

37 (77.1) 27 (57.4) 44 (91.7) 43 (91.5)<br />

a Morphological <strong>and</strong> karyotypic characters.<br />

b Nonmolecular data plus concatenated sequences from five loci.<br />

c In strict consensus <strong>of</strong> minimum-length trees.

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