Boyer diss 2009 1046..

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notch and radial facet on the lateral side, there is not such a pronounced depression as on the opposite side. However, there is a sharp, faint groove caused by a narrow lip that protrudes from the posterior surface of the ulna. Farther distally, the lateral aspect of the shaft obtains a more distinctive, yet still shallow, depression. Toward the distal end of the bone the shaft develops two diverging dorsal ridges. The lateral one approaches the distal radial facet, while the other passes medial to it before meeting up with a surface that is contiguous with the radial facet and the carpal facet more distally. The more lateral of the two ridges appears to be the interosseous crest, while the medial one probably represents the medial edge of the area of origination for the pronator quadratus muscle (George, 1977). The distal end is marked by a dorsodistally-facing, convex facet for the distal radius and the lunate (see below). Distal to this, the styloid process sports a convex, dorsodistomedially facing facet for the triquetrum and pisiform of the proximal carpal row. Function.—The ulnar trochlea complements the morphology of the radius and humerus in the rather flat form and lateral orientation of its radial facet, which would have permitted the head of the radius to rotate on it. A dorsally projecting olecranon process suggests habitually flexed forearms and may even have limited the capacity for full extension, depending on the undistorted size of the olecranon process (Szalay et al., 1975). The only notable muscle scars are the groove on the medial surface of the proximal end, which likely provided a large area for insertion of the flexor carpi ulnaris muscle (George, 1977) and the ridge denoting the edge of the attachment for what was probably a well-developed pronator quadratus muscle (George, 1977). The presence of a 296
distinct, convex distal radial facet reinforces the inference that there was substantial axial mobility in the radius with respect to the ulna. Its location on the dorsal aspect of the ulna is consistent with morphology of the radius, suggesting that the wrist was maintained in a semi-supinated orientation most of the time. Comparison.—In general, the ulna of P. cookei does not differ appreciably from those of other plesiadapids. None of the shape indices in Table 4.6A reveal any quantified differences. Qualitatively comparing more subtle aspects of the morphology, it can be stated that the ulna of P. cookei seems to be unique in the shallowness of the longitudinal groove marking the lateral side of its shaft for origination of extensor musculature. The ulna of P. cookei also appears more gracile than those of other plesiadapids; however, as mentioned, this is not borne out by any measurements (e.g., Table 4.5A: NSV and SSV). Scaphoid Description.—The right scaphoid is preserved (Table 4.6; Fig. 4.7A). It was originally identified by comparisons to the scaphoid of N. intermedius USNM 442229 (Beard, 1993a) and a scaphoid dentally associated to the paromomyid Acidomomys hebeticus (<strong>Boyer</strong> and Bloch, 2008). Aside from being “boat-shaped,” as the etymology of the bone’s name suggests, with a convex proximal articular surface forming the “hull of the boat” and the concave distal articular surface forming the “boat’s interior,” the scaphoid of P. cookei could also be described as “barbell-shaped” because the ventral tubercle is quite large and distinct from the articular surface for the radius. On the proximal surface, the radius facet is triangular to pyriform in outline (Figs. 4.7A, 4.8: 5), 297
Page 1 and 2:
NEW CRANIAL AND POSTCRANIAL REMAINS
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Stony Brook University The Graduate
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postcranial anatomy more accurately
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Table of Contents List of Figures .
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Zygomatic. . . . . . . . . . . . .
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Zygomatic. . . . . . . . . . . . .
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Humerus . . . . . . . . . . . . . .
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Description . . . . . . . . . . . .
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Description . . . . . . . . . . . .
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Craniodental material of Plesiadapi
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Figure 2.25. MNHN CR 965 Plesiadapi
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Figure 4.24. UM 87990 Plesiadapis c
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Table List Chapter 2 Table 2.1. Num
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Table 4.30. Caudal vertebrae measur
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CHAPTER 1: INTRODUCTION Plesiadapif
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primates, sharing many dental featu
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were acquired. Specifically, the
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of the plesiadapiform skeleton. Ext
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Gervais, M.P., 1877. Enumération d
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Szalay, F.S., 1972. Cranial morphol
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CHAPTER 2: A REEVALUATION OF CRANIA
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Information on the cranium of basal
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petrosal bulla predicts that a sutu
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History of descriptive study of ple
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Gingerich (1971) rebutted Szalay (1
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9c, Gingerich (1976) labeled a groo
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portion of the bulla medial to the
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Bloch and Silcox (2006) described t
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MATERIALS AND METHODS Material exam
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whitening, dark and light areas on
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SYSTEMATIC PALEONTOLOGY Class MAMMA
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efore meeting a large, anteroposter
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The canine is a simple, single-root
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existence and/or nature of contacts
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outlined. This includes description
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eneath it while also extending post
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y a pair of parallel grooves (Fig.
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the skull (Fig. 2.1). The length of
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margin clearly had a posteriorly pr
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groove measures about 0.29 mm in di
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2.13: 50). The suture with the supr
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preserved (Fig. 2.15: 55). In fact,
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the posterior septum, a deeply inci
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Plesiadapis tricuspidens MNHN CR 12
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is roughly 2.8 mm long. Medial to t
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is not convoluted like many other s
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110) and the only squamosal/alisphe
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two regions for the internal jugula
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ventral to the sinuous suture (132)
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provides measurements of these and
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of the promontorium of the Pellouin
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seen on the HRxCT scan is expressed
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primates, as well as treeshrews and
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canaliculus are present on the sept
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it is missing from the other side o
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observations and interpretations ma
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REFERENCES Beard, K.C., 1993. Phylo
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Russell, D.E., 1959. Le crâne de P
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TABLES Table 2.1. Numerical list of
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81 - Occipital/petrosal suture (Fig
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Table 2.2. Abbreviations for crania
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Table 2.3a. Petrosal features of pl
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Table 2.4. List of cranial measurem
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Shape variables (Table 2.6) ac/GM -
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Table 2.5. continued Specimen MNHN
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Appendix Table 2.1. Specimens scann
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Fig. 2.39 - bs, Ptr, rtp, s1, s2 Fi
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Figure 2.1. UALVP 46685 Pronothodec
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Figure 2.8. USNM 309902 Nannodectes
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Figure 2.9. USNM 309902 Nannodectes
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Figure 2.10. USNM 309902 Nannodecte
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Figure 2.15. AMNH 17388 Nannodectes
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Figure 2.16. AMNH 17388 Nannodectes
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Figure 2.22. MNHN CR 965, Plesiadap
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Figure 2.26. Pellouin skull Plesiad
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Figure 2.30. MaPhQ 33y Adapis paris
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Figure 2.32. SBU MRd-12 Sciurus car
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Figure 2.33. UMMZ 58983 Tupaia glis
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Figure 2.34. Boyer coll. Marmota mo
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Figure 2.35. UMMZ TS13 Lagostomus m
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Figure 2.36. AMNH 41527 Lagostomus
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Figure 2.37. AMNH 185638 Indri indr
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Figure 2.38. USNM 482353 Ignacius c
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Figure 2.39. UM 108207 Acidomomys h
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Figure 2.40. Reconstruction of ples
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CHAPTER 3: DESCRIPTION OF THE FIRST
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these species. Changing ecological
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Institutional abbreviations AMNH, A
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Methods of examination and document
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SYSTEMATIC PALEONTOLOGY Class MAMMA
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Premaxilla and premaxillary dentiti
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nerve and vessels in life (Fig. 3.5
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identifiable. No ethmoid foramina c
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process is quite large, projecting
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vestibuli. This groove’s point of
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9: 40). The right side reveals an a
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e seen as a wedge-shaped, rugose de
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process appears as solid bone. Admi
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16) for P. tricuspidens and Rose (1
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DENTAL FUNCTIONAL MORPHOLOGY OF P.
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Lower premolar molarization As indi
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SUMMARY AND CONCLUSION The skull of
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REFERENCES Bloch, J.I., Boyer, D.M.
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TABLES Table 3.1. List of anatomica
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Table 3.2. Anatomical abbreviations
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Table 3.3. Size comparison among pl
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Table 3.4 continued. European plesi
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Figure 3.1. Cranium of Plesiadapis
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Figure 3.3. Right maxillary teeth (
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Figure 3.8. Fragment from right nuc
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Figure 3.9. Right promontorium of P
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Figure 3.12. Right dentary of Plesi
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Figure 3.14. A, Plot of relief inde
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CHAPTER 4: THE FIRST KNOWN SKELETON
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among plesiadapiforms (e.g., Szalay
Page 273 and 274: Institutional and collections abbre
Page 275 and 276: CaL - capitulum (of humerus) antero
Page 277 and 278: HSV - head shape variable = ln(DEW/
Page 279 and 280: MSD - mid-shaft dorsoventral or ant
Page 281 and 282: Ry - ray (as in “digit ray”) S-
Page 283 and 284: History of descriptive study of the
Page 285 and 286: illustrations of this material, exc
Page 287 and 288: astragalus and calcaneum was highly
Page 289 and 290: discussion of the femur indicates t
Page 291 and 292: supinator crests. He also noted tha
Page 293 and 294: that it may not even be an archonta
Page 295 and 296: unstudied material. Specifically, h
Page 297 and 298: 5321), some metapodials (MNHN R 529
Page 299 and 300: Gingerich and Gunnell (1992) publis
Page 301 and 302: prehensility they provide, is an in
Page 303 and 304: euarchontans (Fig. 1.1). Their anal
Page 305 and 306: for comparison. These include isola
Page 307 and 308: plesiadapid samples have the same m
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
Page 317 and 318: epicondyle actually projects somewh
Page 319 and 320: cookei is absolutely longer than an
Page 321 and 322: tuberosity. This crest probably del
Page 323: olecranon process to estimate its t
Page 327 and 328: of the midcarpal joint), and its pr
Page 329 and 330: (there is no evidence for more than
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 and 360: The femoral shaft is smooth, lackin
Page 361 and 362: lacking a lateral extension of its
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
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tubercle, which is centrally locate
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Cuboid Description.—The right cub
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Ectocuneiform Description.—A left
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Metatarsals Hallucal metatarsal des
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articulation with the entocuneiform
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medial side facet on MT IV from a v
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Vertebral column Vertebral column d
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measurements, see caption of Fig. 4
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transverse processes, and the poste
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taxa appear to have slightly more p
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dorsoventrally than craniocaudally.
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The zygapophyses increase in size b
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vertebrae. It is also similar to th
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identifications have been reversed.
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preserved. The ribs are slender and
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Carpolestes simpsoni (UM 101963) an
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third metacarpal, similar to arbore
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autapomorphy, because it appears th
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Jenkins (1974) found that Tupaia gl
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Nannodectes and other plesiadapids,
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are consistent with more frequent u
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differences generated from informat
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Perry, M. Silcox, R. Secord and man
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ubriventer: implications for the fu
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Linnaeus, C., 1758. Systema naturae
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Stern, J.T.,Jr., 1988. Essentials o
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Table 4.3A. Measurements of the pro
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Table 4.3C. Comparative shape varia
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Table 4.5A. Measurements and shape
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Table 4.10. Measurements and shape
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Table 4.13. Measurements of plesiad
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Table 4.17B. Measurements of the di
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Table 4.18B. Measurements of the di
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Table 4.20B. Measurements 11-18 of
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Table 4.21A. Measurements 1-10 and
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Table 4.23. Measurements and shape
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Table 4.35. Body segment lengths (m
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Table 4.37A. Parameters for Gingeri
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Table 4.38C. Summary of plesiadapid
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Appendix Table 4.1B. Plesiadapis co
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Appendix Table 4.3. Other plesiadap
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Figure 4.2. Plesiadapis cookei (UM
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Figure 4.4. Plot of principal coord
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Figure 4.6. Surface reconstructions
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Figure 4.10. Surface reconstruction
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Figure 4.14. Plesiadapis cookei or
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Figure 4.17. Plot of principal coor
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Figure 4.30 472
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Figure 4.31. Measurements of astrag
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Figure 4.33 476
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Figure 4.34. Measurements of calcan
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Figure 4.40. Stereophotographic vie
Page 514 and 515:
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Figure 4.46. 490
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Figure 4.47 492
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Figure 4.50. 496
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INTRODUCTION Bloch et al. (2007) an
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have a lacrimal bone that retains i
Page 532 and 533:
Institutional abbreviations AMNH, A
Page 534 and 535:
level cladogram. A total of 33 cran
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plesiadapiform Ignacius graybullian
Page 538 and 539:
RESULTS Phylogenetic reconstruction
Page 540 and 541:
Optimization of postcranial traits
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Therefore, character optimization r
Page 544 and 545:
carpolestid bulla is not split into
Page 546 and 547:
2008). I therefore changed the codi
Page 548 and 549:
Re-coding and optimization of crani
Page 550 and 551:
and paromomyids. This, however, is
Page 552 and 553:
REFERENCES Beard, K.C., 1989. Postc
Page 554 and 555:
Novacek, M.J., 1986. The skull of l
Page 556 and 557:
TABLES Table 5.1. Dental characters
Page 558 and 559:
Table 5.2. Dental character matrix.
Page 560 and 561:
asisphenoid and basioccipital bones
Page 562 and 563:
111 (p3). Deltopectoral crest of hu
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158 (p50). Metatarsal I facet on en
Page 566 and 567:
Table 5.4C. Postcranial characters
Page 568 and 569:
Table 5.7. Posterior carotid forame
Page 570 and 571:
Figure 5.2. 542
Page 572 and 573:
Figure 5.3 544
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Figure 5.4. Plot of posterior carot
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ostral end of the nasals) and prema
Page 578 and 579:
its body size would fit predictions
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vertically-to-caudally projecting t
Page 582 and 583:
More generally speaking, this disse
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Figure 6.1. CT reconstruction of Pl
Page 586 and 587:
BIBLIOGRAPHY Alexander, R.M., Jayes
Page 588 and 589:
Coleman, M. N. and Boyer, D.M. 2008
Page 590 and 591:
Godinot, M., Beard, K.C., 1991. Fos
Page 592 and 593:
MacPhee, R.D.E., 1981. Auditory Reg
Page 594 and 595:
Savage, D.E., Russell, D.E., 1983.
Page 596 and 597:
Szalay, F.S., Drawhorn, G., 1980. E
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