Boyer diss 2009 1046..

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

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described plesiadapid bones including those of P. tricuspidens (MNHN BR-3-L, MNHN R 450, MNHN BR-16-L and MNHN R 444), N. intermedius (USNM 442229), and N. gidleyi (AMNH 17379). They found that these taxa had limbs that were shorter than those of extant gliders, arboreal nongliders and paromomyids, but similar in proportional length to those of terrestrial sciurids. Although the authors did not discuss the significance of this finding, the results support the view of Gingerich (1976). Hamrick (2001) plotted third digit ray proportions (metacarpal, proximal phalanx and intermediate phalanx) of archontan mammals on ternary diagrams (a graph with three axes where each axis represents the length of one of the bones of a digit ray in the form of its percentage of the entire digit ray length). He included measurements from undescribed bones of P. cookei (UM 87990) and found them to plot with scandentians and to be separated from those of modern primates. He argued that euprimate manual digit proportions were a “novel” innovation associated with the evolutionary origin and subsequent adaptive radiation of the clade. Bloch and Boyer (2002) added to Hamrick’s (2001) ternary diagram by plotting digits of P. cookei and other plesiadapiforms (although they do not indicate which particular specimens were plotted). They also provided the first figure (p. 1609, fig. 5B) of a digit ray based on bones of P. cookei (UM 87990). They showed that nonplesiadapid plesiadapiforms plot with euprimates and suggested that P. cookei is derived in having scandentian-like proportions. Thus, they disagreed with Hamrick’s (2001) suggestion that euprimates were characterized by a change in finger proportions compared to plesiadapiforms. Instead, they concluded that long fingers, and the manual 272

prehensility they provide, is an innovation of the ancestor of a clade comprised of euprimates and plesiadapiforms (but probably excluding dermopterans and treeshrews). Youlatos and Godinot (2004) quantitatively compared the morphology of P. tricuspidens and P. n. sp. material from Berru and the early Eocene Le Quesnoy locality, respectively, to that of a sample of extant terrestrial and arboreal rodents. Much of the material listed in their table 1 (p. 105) has been figured or mentioned elsewhere (not including the list from Russell, 1964) including ulnae (MNHN R 546 and MNHN R 443), radii (MNHN R 550), femora (MNHN BR-16-L, MNHN R 408, MNHN R 444) and ungual phalanges (MNHN R 5361, MNHN R 5381, MNHN R 5309). Additionally they analyzed for the first time several new ulnae (MNHN R 411 and MNHN R 615), radii (MNHN R 553 and MNHN R 597), a femur (MNHN R 407), and claws (MNHN R 612- 613). They also included newly recognized uncatalogued specimens of radii and ungual phalanges. The authors listed “MNHN R 542” as a proximal ulna. I could not find this specimen when I visited the MNHN. I did, however, find a proximal ulna with the number MNHN R 452 and presume that this is the specimen to which the authors intended to refer. Russell does not list MNHN R 542 as an element of Plesiadapis. According to Russell (1964: p. 309), “MNHN R 542” is a partial humerus of Pleursapidotherium aumonieri. Youlatos and Godinot also listed “MNHN R 2527,” which I could not locate and Russell did not list. Another problem appears to be their listing of “MNHN R 5370” as a claw; Russell (1964) listed this bone as a metapodial and Beard (1989) confirmed his identification. Youlatos and Godinot also listed “MNHN R 549” as a claw. Again, I could not locate this element and Russell did not list it as an ungual. Instead, Russell (1964: p. 309) listed MNHN R 549 under Pleuraspidotherium 273

prehensility they provide, is an innovation of the ancestor of a clade comprised of<br />

euprimates and plesiadapiforms (but probably excluding dermopterans and treeshrews).<br />

Youlatos and Godinot (2004) quantitatively compared the morphology of P.<br />

tricuspidens and P. n. sp. material from Berru and the early Eocene Le Quesnoy locality,<br />

respectively, to that of a sample of extant terrestrial and arboreal rodents. Much of the<br />

material listed in their table 1 (p. 105) has been figured or mentioned elsewhere (not<br />

including the list from Russell, 1964) including ulnae (MNHN R 546 and MNHN R 443),<br />

radii (MNHN R 550), femora (MNHN BR-16-L, MNHN R 408, MNHN R 444) and<br />

ungual phalanges (MNHN R 5361, MNHN R 5381, MNHN R 5309). Additionally they<br />

analyzed for the first time several new ulnae (MNHN R 411 and MNHN R 615), radii<br />

(MNHN R 553 and MNHN R 597), a femur (MNHN R 407), and claws (MNHN R 612-<br />

613). They also included newly recognized uncatalogued specimens of radii and ungual<br />

phalanges. The authors listed “MNHN R 542” as a proximal ulna. I could not find this<br />

specimen when I visited the MNHN. I did, however, find a proximal ulna with the<br />

number MNHN R 452 and presume that this is the specimen to which the authors<br />

intended to refer. Russell does not list MNHN R 542 as an element of Plesiadapis.<br />

According to Russell (1964: p. 309), “MNHN R 542” is a partial humerus of<br />

Pleursapidotherium aumonieri. Youlatos and Godinot also listed “MNHN R 2527,”<br />

which I could not locate and Russell did not list. Another problem appears to be their<br />

listing of “MNHN R 5370” as a claw; Russell (1964) listed this bone as a metapodial and<br />

Beard (1989) confirmed his identification. Youlatos and Godinot also listed “MNHN R<br />

549” as a claw. Again, I could not locate this element and Russell did not list it as an<br />

ungual. Instead, Russell (1964: p. 309) listed MNHN R 549 under Pleuraspidotherium<br />

273

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