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Boyer diss 2009 1046..

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medial side facet on MT IV from a ventrally placed one. As for dorsal facets, the<br />

ventrally placed facet is larger than the corresponding medial side facet on MT III. The<br />

lateral side of the proximal end of MT IV differs from that of MT III in having a<br />

continuous concave articular surface for the more lateral metatarsal (MT V) with no<br />

nonarticular gaps separating it into dorsal and ventral regions.<br />

In most respects the proximal end of the “set 2” MT IV is similar to that of the<br />

“set 1” element. However, it is diagnostically different in the morphology of the medial<br />

side, dorsal facet for MT III. Specifically, this facet is larger and strongly concave in the<br />

“set 2” MT IV (instead of slightly convex). As a result of these differences in articular<br />

surface morphology, the “set 2” MT IV, which is a left side element, will not articulate<br />

securely with the left side MT III.<br />

Metatarsal V description.—Only a proximal fragment of the right MT V is<br />

preserved (Fig. 4.40B). It is identifiable as MT V by its large peroneal tuberosity.<br />

However, it clearly did not belong to P. cookei, as revealed by MT V’s preserved with<br />

two other plesiadapid skeletons (Table 4.23). Although not described by Beard (1989), a<br />

proximal base and distal shaft of an MT V of Nannodectes intermedius USNM 442229<br />

are preserved. A specimen of cf. P. churchilli (SMM P77.33.517) from Wannagan Creek<br />

in North Dakota also preserves this element (Fig. 4.39B, C). The plesiadapid MT V is<br />

revealed to be treeshrew or dermopteran-like by these specimens. The UM 87990 MT V<br />

does not fit this pattern and does not even articulate well with the “set 1” MT IV.<br />

Presumably, it articulates with the “set 2” MT IV better, however the MT V facet on MT<br />

IV is too broken to assess this possibility.<br />

357

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