Boyer diss 2009 1046..

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

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RESULTS Phylogenetic reconstructions Species level cladistic analysis – 144 trees resulted from analysis of the dental matrix of 32 characters. The strict consensus of these is shown in Figure 5.1A. Plesiadapidae is monophyletic with Elphidotarsius forming the sister taxon of the group. Pronothodectes is the most basal genus of the family. Nannodectes, Chiromyoides, and Platychoerops are monophyletic, and P. cookei is recovered as the sister taxon of Platychoerops. The length of each most parsimonious tree is 66. The consistency index is 59. The retention index is 83. In most respects the reconstructed phylogeny is congruent with that of Gingerich (1976) based on stratophenetic methodology, if less resolved in some ways. Addition of stratigraphic data will likely resolve many of these polytomies. Character optimization - Table 5.3 is a list of characters from Bloch et al. (2007) and seven additional characters. These characters were scored for the crania described in chapters 2 and 3, and postcrania described in Chapter 4. Internal carotid artery functionality was also scored (Table 5.4A-B). These character states were optimized onto the consensus cladogram recovered through the species level analysis. The optimized state for the ancestral node is given in the last row of Table 5.4A-C. A drawing of a cranium based on the ancestral node and P. tricuspidens illustrates the differences that appear to distinguish basal, Pr. gaoi-like taxa, and more derived, later-occurring P. tricuspidens-like taxa (Fig. 5.2). 510

Various plesiadapid taxa differ from the reconstruction representing the ancestral node for Plesiadapidae. For instance, N. gidleyi differs in having an apparently relatively larger glenoid fossa (Table 5.4B: 30) and an internal carotid plexus route that probably did not have an intratympanic route. However, if the posterior carotid foramen is correctly identified in N. gidleyi (Chapter 2), the route for the internal carotid plexus was similar to that of other plesiadapids in being relatively laterally positioned on the basicranium. P. tricuspidens differs in a number of respects illustrated in Figure 5.2: it exhibits a tubular external auditory meatus (Table 5.4A: 3), a narrow nasal bone (Table 5.4A: 16), a broad premaxilla/frontal contact (Table 5.4B: 27), and an annular component to its ectotympanic that flares substantially beyond the bony struts connecting it to the bullar wall (Table 5.4B: 28). Additionally, P. tricuspidens lacks exposure of molar tooth roots other than the distobuccal root of M 3 (Table 5.4B: 29), has a proportionally larger glenoid fossa (Table 5.4B: 30), and appears to have a less posteriorly projecting nuchal crest (Table 5.4B: 31). P. cookei is similar to P. tricuspidens in the tubular form of its external auditory meatus and in the lack of dorsal exposure of most tooth roots on its maxilla in the orbit. Major features shared by basal and most derived plesiadapids include a premaxilla that contacts the frontal bone, an apparently petrosal bulla, and an internal carotid artery that has a posterolateral entrance, is non-functional, and crosses the lateral aspect of the promontorium (see chapters 2-3). Plesiadapids have previously been considered to lack a lacrimal tubercle. However, as discussed in Chapter 2, the best preserved lacrimal specimen of P. tricuspidens (MNHN CR 126) has a blunt lacrimal tubercle. 511

Various plesiadapid taxa differ from the reconstruction representing the ancestral<br />

node for Plesiadapidae. For instance, N. gidleyi differs in having an apparently relatively<br />

larger glenoid fossa (Table 5.4B: 30) and an internal carotid plexus route that probably<br />

did not have an intratympanic route. However, if the posterior carotid foramen is<br />

correctly identified in N. gidleyi (Chapter 2), the route for the internal carotid plexus was<br />

similar to that of other plesiadapids in being relatively laterally positioned on the<br />

basicranium. P. tricuspidens differs in a number of respects illustrated in Figure 5.2: it<br />

exhibits a tubular external auditory meatus (Table 5.4A: 3), a narrow nasal bone (Table<br />

5.4A: 16), a broad premaxilla/frontal contact (Table 5.4B: 27), and an annular component<br />

to its ectotympanic that flares substantially beyond the bony struts connecting it to the<br />

bullar wall (Table 5.4B: 28). Additionally, P. tricuspidens lacks exposure of molar tooth<br />

roots other than the distobuccal root of M 3 (Table 5.4B: 29), has a proportionally larger<br />

glenoid fossa (Table 5.4B: 30), and appears to have a less posteriorly projecting nuchal<br />

crest (Table 5.4B: 31). P. cookei is similar to P. tricuspidens in the tubular form of its<br />

external auditory meatus and in the lack of dorsal exposure of most tooth roots on its<br />

maxilla in the orbit.<br />

Major features shared by basal and most derived plesiadapids include a<br />

premaxilla that contacts the frontal bone, an apparently petrosal bulla, and an internal<br />

carotid artery that has a posterolateral entrance, is non-functional, and crosses the lateral<br />

aspect of the promontorium (see chapters 2-3). Plesiadapids have previously been<br />

considered to lack a lacrimal tubercle. However, as discussed in Chapter 2, the best<br />

preserved lacrimal specimen of P. tricuspidens (MNHN CR 126) has a blunt lacrimal<br />

tubercle.<br />

511

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