Boyer diss 2009 1046..

Boyer diss 2009 1046.. Boyer diss 2009 1046..

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Major cranial differences between Plesiadapis cookei and P. tricuspidens The crania of P. cookei and P. tricuspidens are not highly divergent. In fact, they are uniquely similar among known plesiadapid skulls in their laterally expanded, tubular external auditory meati, and in the minimal exposure of the molar roots on the dorsal surface of their maxillae. On the other hand, P. cookei differs distinctly from P. tricuspidens in having proportionally broader nasals (Table 2.6: N/GM), and a proportionally smaller glenoid fossa (Table 2.6: Gld/GM). Additionally, P. cookei appears to differ from P. tricuspidens in having an ectotympanic ring that does not flare beyond its attachment to the bullar part of the ectotympanic as substantially, and possibly in having a more posteriorly projecting nuchal crest. Interestingly, the features separating P. cookei from P. tricuspidens, also separate smaller North American plesiadapids from P. tricuspidens, including P. anceps, N. intermedius, N. gidleyi, and Pr. gaoi (see Chapter 2). Some previously undocumented dental differences between P.cookei and P. tricuspidens are also revealed by UM 87990: unlike P. tricuspidens, P. cookei lacks a P 2 and a has more molariform P 4 . IMPLICATIONS OF CRANIODENTAL MATERIAL FOR BODY SIZE IN PLESIADAPIDAE Though it is clear that both P. cookei and P. tricuspidens were absolutely large among plesiadapids generally, the comparison of body size in these species has remained ambiguous. P. cookei has molar teeth with occlusal areas that are 140% (M 1 ), 127% (M 2 ) and 119% (M 3 ) larger than those of P. tricuspidens [data from Gingerich (1976: table A- 202

16) for P. tricuspidens and Rose (1981: table 14) for P. cookei]. These data lead to the hypothesis that P. cookei was a bigger animal than P. tricuspidens (Gingerich et al., 1982; Fleagle, 1999). However, side-by-side comparison of the UM 87990 cranium and MNHN CR 125 (or the Pellouin skull) in dorsal or ventral view shows that the P. tricuspidens specimens dwarf P. cookei, the opposite of what tooth size differences would lead one to predict. Close inspection reveals that this contradiction is mainly due to differential patterns of deformation among the different skulls. Whereas UM 87990 is compressed anteroposteriorly and mediolaterally so that it is now smaller in these dimensions than it was in life, the P. tricuspidens specimens are compressed dorsoventrally, so that they probably still retain their transverse plane dimensions. The degree to which size differences have been accentuated is revealed by a series of 39 measurements on individual cranial bones (Table 2.5: Table 3.3). This exercise shows that the skulls of P. cookei and P. tricuspidens are almost identical in the size of almost every feature measured except for the glenoid fossae, which are distinctly larger in the two P. tricuspidens specimens. Specifically, measurements from all regions of the P. cookei skull (UM 87990) are, on average, 99% the size of those of both skulls of P. tricuspidens (MNHN CR 125 and the Pellouin skull). The value “99%” is literally the antilogged average of 39 natural log ratios of P. cookei to P. tricuspidens cranial measurements. In other words, it is an average of 39 direct comparisons. A less direct comparison using a geometric mean of these 39 measurements yields a slightly different but comparable result. The geometric mean of the P. cookei measurements is 10.7, while that of MNHN CR 125 is 10.6, suggesting that, instead, the P. tricuspidens skull is 99% the size of that of P. cookei. Comparisons between P. cookei and a sample of P. 203

16) for P. tricuspidens and Rose (1981: table 14) for P. cookei]. These data lead to the<br />

hypothesis that P. cookei was a bigger animal than P. tricuspidens (Gingerich et al.,<br />

1982; Fleagle, 1999). However, side-by-side comparison of the UM 87990 cranium and<br />

MNHN CR 125 (or the Pellouin skull) in dorsal or ventral view shows that the P.<br />

tricuspidens specimens dwarf P. cookei, the opposite of what tooth size differences<br />

would lead one to predict. Close inspection reveals that this contradiction is mainly due<br />

to differential patterns of deformation among the different skulls. Whereas UM 87990 is<br />

compressed anteroposteriorly and mediolaterally so that it is now smaller in these<br />

dimensions than it was in life, the P. tricuspidens specimens are compressed<br />

dorsoventrally, so that they probably still retain their transverse plane dimensions. The<br />

degree to which size differences have been accentuated is revealed by a series of 39<br />

measurements on individual cranial bones (Table 2.5: Table 3.3). This exercise shows<br />

that the skulls of P. cookei and P. tricuspidens are almost identical in the size of almost<br />

every feature measured except for the glenoid fossae, which are distinctly larger in the<br />

two P. tricuspidens specimens. Specifically, measurements from all regions of the P.<br />

cookei skull (UM 87990) are, on average, 99% the size of those of both skulls of P.<br />

tricuspidens (MNHN CR 125 and the Pellouin skull). The value “99%” is literally the<br />

antilogged average of 39 natural log ratios of P. cookei to P. tricuspidens cranial<br />

measurements. In other words, it is an average of 39 direct comparisons. A less direct<br />

comparison using a geometric mean of these 39 measurements yields a slightly different<br />

but comparable result. The geometric mean of the P. cookei measurements is 10.7, while<br />

that of MNHN CR 125 is 10.6, suggesting that, instead, the P. tricuspidens skull is 99%<br />

the size of that of P. cookei. Comparisons between P. cookei and a sample of P.<br />

203

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