Boyer diss 2009 1046..
Boyer diss 2009 1046.. Boyer diss 2009 1046..
more abduction could have really occured, but lateral rotation, followed by extension, allowed the condyles to shift farther caudally. Relatively small greater and third trochanters, and a medially projecting (rather than posteriorly projecting) lesser trochanter are further indicative that the femur was not flexed and extended forcefully using the gluteal musculature (Sargis, 2002b). However, the expansive trochanteric fossa and expanded area distal to the intertrochanteric crest for the obturators and quadratus femoris, respectively, would have given the limb a capacity for powerful abduction and lateral rotation of a flexed, adducted thigh. The large, medially projecting lesser trochanter would have provided a large lever arm for the iliopsoas muscle: from a somewhat extended, abducted, medially rotated posture, iliopsoas would also have served to flex, adduct, and laterally rotate the femur. The proximally restricted patellar groove and distally extensive condyles suggest that full extension of the knee was infrequent or impossible, and that a flexed knee was a habitual posture. Relatively shallow femoral condyles suggest extension of the knee was not particularly forceful (Beard, 1989; Sargis, 2002b) when it occurred. The pattern of buttressing of the patellar groove margins are consistent with a posture wherein the femur was habitually flexed and abducted, and the knees were flexed (Boyer and Bloch, 2008). Comparison.—The femur of plesiadapids does not exhibit a drastic amount of variation in the species for which it is known. Most aspects of the description given for P. cookei apply equally to P. tricuspidens, N. gidleyi and a newly recognized specimen of N. intermedius (Table 4.17A-C). The description of the femoral head of P. cookei differs from that given by Beard (1989) for other plesiadapids. He characterized the plesadapid femoral head as being spherical, having a centrally placed fovea capitis femoris, and as 332
lacking a lateral extension of its articular facet. He made this point in order to contrast plesiadapids with non-plesiadapid plesiadapiforms (Beard, 1989: fig. 76). While I agree that plesiadapids differ from non-plesiadapids to a degree, based on my observations of the entire collection of P. tricuspidens in Paris and N. gidleyi, almost all appear to exhibit the three features they were said to lack. Plesiadapids appear to differ from nonplesiadapids in having a slightly less posteriorly positioned fovea capitis femoris and in having a smaller lateral articular surface extension. It is important to make this clear because of the functional implications for these features, as discussed above. Because of the large sample of P. tricuspidens from France, an assessment of shape variation can be done with the potential for statistical confidence. Using t-tests on data from Table 4.17C, it can be shown that the femur of P. cookei differs from all relatively complete femora from the Berru locality in France in being longer (ln[Le]: t = -5.98, P = 0.0003), more gracile (SSV: t = -7.06, P = 0.0001), having a proportionally smaller femoral head (HShV:t = -13.25, P
- Page 309 and 310: Organization of results Each bone i
- Page 311 and 312: Bloch and Boyer (2002) and N. inter
- Page 313 and 314: clavicle reflects some basic aspect
- Page 315 and 316: Humerus Description.—The right an
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- Page 321 and 322: tuberosity. This crest probably del
- Page 323 and 324: olecranon process to estimate its t
- Page 325 and 326: distinct, convex distal radial face
- Page 327 and 328: of the midcarpal joint), and its pr
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- Page 331 and 332: matches the opposing facet on the t
- Page 333 and 334: mobility at the trapezoid-trapezium
- Page 335 and 336: Function.—The three proximal carp
- Page 337 and 338: the bone presently being described:
- Page 339 and 340: the “set 2” MC II is a larger,
- Page 341 and 342: differs from MC II and III in havin
- Page 343 and 344: even more pronounced. The distal en
- Page 345 and 346: etween the distal carpals and the
- Page 347 and 348: have stouter shaft diameters for th
- Page 349 and 350: difference makes them more like kno
- Page 351 and 352: antipronograde clinging postures, o
- Page 353 and 354: foramina, and faces slightly proxim
- Page 355 and 356: spine at the superior tip of the il
- Page 357 and 358: the thigh (Gambaryan, 1974). The ha
- Page 359: The femoral shaft is smooth, lackin
- Page 363 and 364: The anteromedial side of the tibial
- Page 365 and 366: fibular notch and the strong crest
- Page 367 and 368: to the peroneal surface. The perone
- Page 369 and 370: could even be described as having t
- Page 371 and 372: Function.—The functional features
- Page 373 and 374: flexor fibularis groove surface. Ex
- Page 375 and 376: tubercle, which is centrally locate
- Page 377 and 378: Cuboid Description.—The right cub
- Page 379 and 380: Ectocuneiform Description.—A left
- Page 381 and 382: Metatarsals Hallucal metatarsal des
- Page 383 and 384: articulation with the entocuneiform
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- Page 387 and 388: Vertebral column Vertebral column d
- Page 389 and 390: measurements, see caption of Fig. 4
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- Page 393 and 394: taxa appear to have slightly more p
- Page 395 and 396: dorsoventrally than craniocaudally.
- Page 397 and 398: The zygapophyses increase in size b
- Page 399 and 400: vertebrae. It is also similar to th
- Page 401 and 402: identifications have been reversed.
- Page 403 and 404: preserved. The ribs are slender and
- Page 405 and 406: Carpolestes simpsoni (UM 101963) an
- Page 407 and 408: third metacarpal, similar to arbore
- Page 409 and 410: autapomorphy, because it appears th
more abduction could have really occured, but lateral rotation, followed by extension,<br />
allowed the condyles to shift farther caudally. Relatively small greater and third<br />
trochanters, and a medially projecting (rather than posteriorly projecting) lesser<br />
trochanter are further indicative that the femur was not flexed and extended forcefully<br />
using the gluteal musculature (Sargis, 2002b). However, the expansive trochanteric fossa<br />
and expanded area distal to the intertrochanteric crest for the obturators and quadratus<br />
femoris, respectively, would have given the limb a capacity for powerful abduction and<br />
lateral rotation of a flexed, adducted thigh. The large, medially projecting lesser<br />
trochanter would have provided a large lever arm for the iliopsoas muscle: from a<br />
somewhat extended, abducted, medially rotated posture, iliopsoas would also have served<br />
to flex, adduct, and laterally rotate the femur. The proximally restricted patellar groove<br />
and distally extensive condyles suggest that full extension of the knee was infrequent or<br />
impossible, and that a flexed knee was a habitual posture. Relatively shallow femoral<br />
condyles suggest extension of the knee was not particularly forceful (Beard, 1989; Sargis,<br />
2002b) when it occurred. The pattern of buttressing of the patellar groove margins are<br />
consistent with a posture wherein the femur was habitually flexed and abducted, and the<br />
knees were flexed (<strong>Boyer</strong> and Bloch, 2008).<br />
Comparison.—The femur of plesiadapids does not exhibit a drastic amount of<br />
variation in the species for which it is known. Most aspects of the description given for P.<br />
cookei apply equally to P. tricuspidens, N. gidleyi and a newly recognized specimen of N.<br />
intermedius (Table 4.17A-C). The description of the femoral head of P. cookei differs<br />
from that given by Beard (1989) for other plesiadapids. He characterized the plesadapid<br />
femoral head as being spherical, having a centrally placed fovea capitis femoris, and as<br />
332