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Boyer diss 2009 1046..

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INTRODUCTION<br />

Among North American plesiadapids (Fig. 1.1), one of the latest occurring and<br />

largest species is Plesiadapis cookei (Jepsen, 1930; Gingerich, 1976). The only known<br />

skull and skeleton of P. cookei, UM 87990, was discovered in late Paleocene strata of the<br />

Clarks Fork Basin in 1987 (Gunnell and Gingerich, 1987; Gingerich and Gunnell, 1992;<br />

Gingerich and Gunnell, 2005). The specimen has not yet received a thorough description<br />

or analysis despite the fact that it is arguably the most completely preserved skeleton of a<br />

plesiadapiform yet recovered (Bloch and <strong>Boyer</strong>, 2007).<br />

The relative completeness of the skeleton allows for documentation of inter- and<br />

intra-limb skeletal element proportions, and assessment of likely habitual configurations<br />

and ranges of mobility of the major joints of the limbs. Estimates of the latter two<br />

parameters have never been made for the radiocarpal and mid-carpal joints.<br />

An initial obstacle to study of this fossil was its preservation in a freshwater<br />

limestone nodule along with an individual of Uintacyon, a similarly sized apparently<br />

arboreal carnivoran (Carnivora, Miacidae): this made the process of preparation and<br />

documentation difficult. The skeletons were prepared using acid reduction techniques<br />

described in Bloch and <strong>Boyer</strong> (2001). Detailed records of skeletal associations were not<br />

kept and there is thus substantial confusion as to which postcranial elements were<br />

originally components of P. cookei and which belong to Uintacyon. This uncertainty is<br />

becoming increasingly minor due to recent description of plesiadapiform specimens with<br />

documented skeletal-dental associations (e.g., Beard, 1989; Bloch et al., 2007). Some<br />

elements are easily identified as belonging to P. cookei, because they are well known<br />

242

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