Boyer diss 2009 1046..

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and paromomyids. This, however, is actually what is suggested by one of the MP trees resulting from revision and reanalysis of the Bloch and Silcox (2006) matrix (Fig. 5.3B), even though it contains no dental characters. Results of the analysis of modified character matrices notwithstanding, the phylogenetic significance of the foregoing facts regarding morphology of paromomyids, plesiadapids, and carpolestids is unclear. Cranial and postcranial similarities uniting paromomyids and plesiadapids, and postcranial similarities uniting carpolestids and euprimates, may mean that carpolestids along with some other “plesiadapoids” (of Bloch et al., 2007) are closer to Euprimates within a “plesiadapoid + euprimate” clade than to plesiadapids. In other words, Plesiadapoidea may be paraphyletic with respect to Euprimates. In this case a topology similar to that depicted in Figure 5.3A, or that recovered by the cladistic analysis of postcranial characters by Bloch and <strong>Boyer</strong> (2002) may be closer to the truth. It is important to note that the decrease in tree length and the increase in consistency index that resulted from analysis of the modified matrices suggest that the recovered topologies are more parsimonious than those of the original matrices. This means that the newly encoded morphology of plesiadapids can be considered as actually strengthening the phylogenetic hypothesis of Bloch et al. (2007), although this may not be intuitive, as revealed by the above discussion. Clearly, there is much still to be learned regarding the phylogenetic relationships among various plesiadapiforms and extant euarchontan mammals including dermopterans, treeshrews and euprimates. New matrices that more intensively sample 522
the anatomy of a broader array of relevant taxa, and the discovery of more plesiadapiform fossils are necessary to increase knowledge on this subject ACKNOWLEDGMENTS I thank K. C. Beard for access to undescribed material of Ch. caesor and N. gazini from the Carnegie Museum of Natural History. I thank M. O’Leary for encouraging me to assess features characterizing basal plesiadapids in a more organized, better documented, and more methodologically rigorous fashion than I had done previously. I thank M. Silcox for forwarding me the data from Kay et al. (1992) presented in Table 5.7. D. Krause, M. O’Leary, J. Fleagle, W. Jungers, and P .Gingerich read and enhanced previous versions of this manuscript. 523
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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
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Institutional and collections abbre
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CaL - capitulum (of humerus) antero
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HSV - head shape variable = ln(DEW/
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MSD - mid-shaft dorsoventral or ant
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Ry - ray (as in “digit ray”) S-
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History of descriptive study of the
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illustrations of this material, exc
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astragalus and calcaneum was highly
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discussion of the femur indicates t
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supinator crests. He also noted tha
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that it may not even be an archonta
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unstudied material. Specifically, h
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5321), some metapodials (MNHN R 529
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Gingerich and Gunnell (1992) publis
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prehensility they provide, is an in
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euarchontans (Fig. 1.1). Their anal
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for comparison. These include isola
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plesiadapid samples have the same m
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Organization of results Each bone i
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Bloch and Boyer (2002) and N. inter
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clavicle reflects some basic aspect
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Humerus Description.—The right an
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epicondyle actually projects somewh
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cookei is absolutely longer than an
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tuberosity. This crest probably del
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olecranon process to estimate its t
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distinct, convex distal radial face
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of the midcarpal joint), and its pr
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(there is no evidence for more than
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matches the opposing facet on the t
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mobility at the trapezoid-trapezium
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Function.—The three proximal carp
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the bone presently being described:
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the “set 2” MC II is a larger,
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differs from MC II and III in havin
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even more pronounced. The distal en
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etween the distal carpals and the
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have stouter shaft diameters for th
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difference makes them more like kno
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antipronograde clinging postures, o
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foramina, and faces slightly proxim
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spine at the superior tip of the il
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the thigh (Gambaryan, 1974). The ha
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The femoral shaft is smooth, lackin
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lacking a lateral extension of its
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The anteromedial side of the tibial
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fibular notch and the strong crest
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to the peroneal surface. The perone
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could even be described as having t
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Function.—The functional features
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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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Page 500 and 501: Figure 4.30 472
Page 502 and 503: Figure 4.31. Measurements of astrag
Page 504 and 505: Figure 4.33 476
Page 506 and 507: Figure 4.34. Measurements of calcan
Page 508 and 509: Figure 4.36. Plesiadapis cookei (UM
Page 512 and 513: Figure 4.40. Stereophotographic vie
Page 518 and 519: Figure 4.46. 490
Page 520 and 521: Figure 4.47 492
Page 524 and 525: Figure 4.50. 496
Page 526 and 527: Figure 4.51. Surface reconstruction
Page 528 and 529: INTRODUCTION Bloch et al. (2007) an
Page 530 and 531: 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
Page 536 and 537: plesiadapiform Ignacius graybullian
Page 538 and 539: RESULTS Phylogenetic reconstruction
Page 540 and 541: Optimization of postcranial traits
Page 542 and 543: 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 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
Page 564 and 565: 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
Page 574 and 575: Figure 5.4. Plot of posterior carot
Page 576 and 577: ostral end of the nasals) and prema
Page 578 and 579: its body size would fit predictions
Page 580 and 581: vertically-to-caudally projecting t
Page 582 and 583: More generally speaking, this disse
Page 584 and 585: 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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