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Journal of Paleontology 92(2):272–288
12 3 ep 1
ep 1 ep 2 ep 3
ep 2 ep 4
ep 5 ep 3 ep 3
ep 4 ep 5
Figure 4. Comparison of frill ornamentations of (1) Albertaceratops nesmoi in Ryan (2007), (2) previous reconstruction of Medusaceratops lokii frill in Ryan et al. (2010) (gray part represents where the holotype [WDC-DJR-001] corresponds), and (3) new reconstruction of M. lokii frill in this study, mainly based on ROM 73832, ROM 73836, and WDC-DJR-001. Abbreviation: ep, epiparietal.
centrosaurines in that the body exhibits a slight torsion such that its medial portion is located on the dorsal surface of the posterior ramus, but the lateral portion is on the posterior margin (Fig. 3.1–3.3). This epiparietal is proportionally broad and low (114.2 by 15.7mm), but projects forward (Fig. 3.1). Although smaller, it is most similar in morphology and position to the ep 1 of Xenoceratops foremostensis Ryan, Evans, and Shepherd, 2012 (P2 in Ryan et al., 2012) among known centrosaurines. ROM 73836 (Fig. 3.8–3.10).—ROM 73836 is an antero-
lateral segment of the parietal that includes the three lateralmost epiparietals (ep 3–5, also see description of WDC-DJR-001 below) and the squamosal contact of the right lateral ramus. Although all three epiparietals are completely fused, the boundary between the epiparietals and the underlying parietal ramus is clearly delineated (Fig. 3.9). On both dorsal and ventral surfaces, the specimen exhibits the combination of a long-grained texture on the lateral side and adult bone texture on themedial side of the lateral parietal ramus (Fig. 3.10). Note that the long-grained texture is always proximally associated with the mottled texture but not the adult texture in centrosaurines (e.g., Avaceratops, “Brachyceratops,”“Monoclonius,” Coronosaurus brinkmani, Centrosaurus, Styracosaurus, Pachyrhinosaurus) that were examined by Brown et al. (2009). The intriguing mixture of textures on ROM73836may suggest a unique ontogenetic textual transition in Medusaceratops. The squamosal contact is rugose and convex, which is typical of centrosaurines but not known in chasmosaurines (Dodson et al., 2004). The two epiparietals closest to the squamosal contact (ep 4
and 5) have a low and rounded triangular morphology when viewed dorsally, similar to unmodified epiparietals in other centrosaurines. Comparatively, the epiparietal (ep 3) posterior to these has a shorter base and a tall, triangular profile with an acute apex (Fig. 3.9). Ep 3 closely resembles the morphology and proportions of the lateral epiparietals on the holotype of Albertaceratops (TMP 2001.026.0001). All of the epiparietals on ROM 73836 are strongly imbricated (Fig. 3.8), and the
squamosal contact is convex, both of which support a centrosaurine assignment for the Mansfield bonebed material (Dodson et al., 2004). WDC-DJR-001 (holotype, Fig. 2.1–2.4).—Part of the
posterior ramus and all of the lateral ramus of the parietal are preserved on WDC-DJR-001, the holotype of M. lokii. Long- grained bone texture occurs on the lateral side of the lateral ramus, as seen on ROM 73836. The posterior ramus thickness (28.1mm) is also similar to that ofROM73832, the midline bar. Ryan et al. (2010) recognized only three epiparietals on this specimen: from medial to lateral these are; a large, wide-based, and pachyostotic hook; a smaller lobe-shaped process; and a round triangular-shaped epiparietal (Ryan et al., 2010). However, comparisons toROM73832 andROM73836 suggest that WDC-DJR-001 actually possesses two previously uniden- tified epiparietal loci, for a total of five. The additional epiparietals include a diminutive epiparietal
medial to the large pachyostotic hook, which we interpret as ep 1, and an open sutural locus for ep 5. The medialmost epiparietal (ep 1) is represented by a small eminence with a porous texture on the posterodorsal margin of the posterior ramus (Fig. 2.2, 2.3). Although the size of the epiparietal differs from the ep 1 on ROM 73832, the incipient nature and the location of these epiparietals on the holotype and ROM 73832 suggests that they are homologous. Other parietals exhibit the presence of a variably sized epiparietal (ep 1) medial to the enlarged pachyostotic hook (ep 2) (see below for detailed description of WDC-DJR-002, ROM 73837 [Fig. 3.6, 3.7] and TMP 2002.069.0006). The smaller pachyostotic process (ep 3) and the round
triangular-shaped epiparietal (ep 4) are imbricated (Fig. 2.4). The pattern of imbrication indicates that the holotype preserves the left side of the frill, instead of the right side as Ryan et al. (2010) originally described. According to the re-orientation, the large pachyostotic hook (ep 2) slightly flexes ventrally at its base and has a distinct margin of the overgrowth on the ramus ventrally, which is similar to the condition of P1 and 2 of
ep 2
ep 1
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