Foraminacephale (meaning "foramina head") is a genus of pachycephalosaurid dinosaur from Late Cretaceous (Campanian stage) deposits of Canada.[1]
| Foraminacephale Temporal range: Late Cretaceous,
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| Holotype specimen CMN 1423 | |
Scientific classification 
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| Domain: | Eukaryota |
| Kingdom: | Animalia |
| Phylum: | Chordata |
| Clade: | Dinosauria |
| Clade: | †Ornithischia |
| Clade: | †Neornithischia |
| Clade: | †Pachycephalosauria |
| Family: | †Pachycephalosauridae |
| Genus: | †Foraminacephale Schott & Evans, 2016 |
| Species: | †F. brevis
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| Binomial name | |
| †Foraminacephale brevis (Lambe, 1918)
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| Synonyms | |
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Description
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Foraminacephale, as a pachycephalosaurid, was a small, bipedal herbivore with a thickened dome on its skull. In 2016, Gregory S. Paul estimated its length at 1.5 metres (4.9 ft), its weight at 10 kilograms (22 lb).[2] In Foraminacephale, the top surface of the dome is punctuated by many small pits, the eponymous foramina; the dome itself consists of a large, central lobe with a sloped frontal half, and two smaller lateral lobes at the front.[3] The squamosal bone forms a tall bar of completely smooth bone underneath the dome, save for six bony nodes that line the bottom edge of the dome and an additional "corner" node just below. These features differentiate Foraminacephale from all other pachycephalosaurids.[1]
Unlike Stegoceras, Hanssuesia, and Colepiocephale, the parietal bone of Foraminacephale (which constitutes the back part of the dome) projects backwards and downwards over the base of the skull.[3] Two traits also differentiate Foraminacephale from Sphaerotholus and Prenocephale: there are prominent grooves between the central lobe and the lateral lobes, and the opening of the temporal bone is slit-like.[1] Micro-CT scans of a potential specimen, identified as cf. Foraminacephale brevis, support that pachycephalosaurids likely engaged in head-butting.[4]
Ontogeny
editAs with Stegoceras,[5] the wide age range present in specimens of Foraminacephale allows for analysis of the ontogeny, or growth, of the dome. Measurements of 27 different points on 21 Foraminacephale skulls showed that the dome became proportionally taller with age, but did not become significantly wider. Histology of the specimens showed that the domes became less porous with age - the smallest specimen's skull was 1.67% empty space, while the largest specimen's skull was 0.25% empty space. Generally, the frontal part of the dome was more porous than the parietal part.[1]
The growth series of the dome allows Foraminacephale to be differentiated further from Stegoceras. In young Stegoceras, the dome is flat; however, in even the smallest Foraminacephale specimens, the parietal is already slightly domed. The supratemporal fenestrae on the top of the skulls of Foraminacephale are slit-like, as opposed to Stegoceras where they are round, and they seal shut very early in ontogeny as opposed to remaining open more-or-less throughout the animal's lifespan. The amount of empty space in the skull roof was also smaller relative to Stegoceras, and more similar to Acrotholus. Furthermore, in Foraminacephale, the squamosal and postorbital bones became part of the dome much quicker, the dome thickened at a slower rate, and the sides of the dome were less angled than in Stegoceras.[1]
Discovery and naming
editThe holotype of Foraminacephale is CMN 1423, a nearly complete frontoparietal dome collected in Dinosaur Provincial Park, Alberta in 1902 and reported on during the same year.[6] The layers of rock where the specimen were found belong to the Dinosaur Park Formation of the Belly River Group. Various other fragments of the skull are also known from the Dinosaur Park Formation, representing juvenile, subadult, and adult individuals.[1]
Although it has been reported that many specimens are known from the contemporary Oldman Formation,[7] only one (catalogued as TMP 2015.044.0041) can definitely be assigned to Foraminacephale. Another specimen from the Horseshoe Canyon Formation formerly assigned to Foraminacephale, CMN 11316, was re-identified as a small, juvenile indeterminate pachycephalosaurine.[1]
CMN 1423 was first assigned to a new species of Stegoceras by Lawrence Lambe in 1918;[8] there was considerable debate over whether "S." brevis represented a truly distinct animal or simply a morph, perhaps the female, of S. validum.[9][10][11] Later, it was assigned to Prenocephale by Robert M. Sullivan in 2000,[3] and then it was assigned to Sphaerotholus by Longrich, Sankey & Tanke in 2010.[12] In 2011, Ryan Schott suggested a new generic name, Foraminacephale, in his Master of Science thesis, resulting in a new combination Foraminacephale brevis.[13] It remained an invalid nomen ex dissertatione until Schott and David Evans formally renamed "S." brevis to Foraminacephale brevis in 2016. The generic name combines Latin foramina ("foramina") with cephale, Latinised Greek for "head", referring to the many pits that covered the top of its dome.[1]
Classification
editA phylogenetic analysis in 2016 found that Foraminacephale was a member of the Pachycephalosaurinae, in a more derived position than Stegoceras, but in a more basal position than Prenocephale. The consensus of the phylogenetic trees recovered is shown below.[1]
The topology of this phylogenetic tree is not very stable, likely due to the incompleteness of most pachycephalosaur specimens.[1]
Paleoecology
editThe Belly River Group is particularly rich in pachycephalosaur remains; 70% of all known pachycephalosaur fossils come from this region. Because of a lack of understanding of pachycephalosaur ontogeny, various authors have assigned this material to anywhere from a single species, Stegoceras validum, to four different genera. This has significant implications for the Late Cretaceous biodiversity of herbivorous dinosaurs. The 2016 description of Foraminacephale recognized four distinct species of pachycephalosaur from the Belly River Group: Stegoceras, Foraminacephale, Hanssuesia, and Colepiocephale, although the specimens that have been referred to Hanssuesia likely represent more than one of the existing species.[1]
See also
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References
edit- ^ a b c d e f g h i j k Schott, R.K.; Evans, D.C. (2016). "Cranial variation and systematics of Foraminacephale brevis gen. nov. and the diversity of pachycephalosaurid dinosaurs (Ornithischia: Cerapoda) in the Belly River Group of Alberta, Canada". Zoological Journal of the Linnean Society. doi:10.1111/zoj.12465.
- ^ Paul, Gregory S. (2016). The Princeton Field Guide to Dinosaurs: Second Edition. Princeton, New Jersey: Princeton University Press. p. 268. ISBN 978-0-691-16766-4.
- ^ a b c Sullivan, R.M. (2000). "Prenocephale edmontonensis (Brown & Schlaikjer) new comb. and P. brevis (Lambe) new comb. (Dinosauria: Ornithischia: Pachycephalosauria) from the Upper Cretaceous of North America". In Lucas, S.G.; Heckert, A.B. (eds.). Dinosaurs of New Mexico. New Mexico Museum of Natural History and Science Bulletin. Vol. 17. pp. 177–190.
- ^ Dyer, Aaron D.; LeBlanc, Aaron R.H.; Doschak, Michael R.; Currie, Philip J. (2021). "Taking a crack at the dome: histopathology of a pachycephalosaurid (Dinosauria: Ornithischia) frontoparietal dome". Biosis: Biological Systems. 2 (2): 248–270. doi:10.37819/biosis.002.02.0101.
- ^ Schott, R.K.; Evans, D.C.; Goodwin, M.B.; Horner, J.R.; Brown, C.M.; Longrich, N.R. (2011). "Cranial Ontogeny in Stegoceras validum (Dinosauria: Pachycephalosauria): A Quantitative Model of Pachycephalosaur Dome Growth and Variation". PLOS ONE. 6 (6): e21092. Bibcode:2011PLoSO...621092S. doi:10.1371/journal.pone.0021092. PMC 3126802. PMID 21738608.
- ^ Lambe L. M. (1902). New genera and species from the Belly River series (Mid-Cretaceous). Contributions to Canadian Paleontology, Geological Survey of Canada 3: 25–81.
- ^ Sullivan, R.M. (2006). "A taxonomic review of the Pachycephalosauridae (Dinosauria: Ornithischia)" (PDF). In Lucas, S.G.; Sullivan, R.M. (eds.). Late Cretaceous vertebrates from the Western Interior. New Mexico Museum of Natural History and Science Bulletin. Vol. 35. pp. 347–365. Archived from the original (PDF) on 2007-09-27. Retrieved 2016-11-26.
- ^ Lambe, L.M. (1918). "The Cretaceous genus Stegoceras typifying a new family referred provisionally to the Stegosauria". Proceedings and Transactions of the Royal Society of Canada. Series 3. 12: 23–36.
- ^ Brown, B.; Schlaikjer, E.M. (1943). "A study of the troodont dinosaurs with the description of a new genus and four new species". Bulletin of the American Museum of Natural History. 82: 121–149. hdl:2246/387.
- ^ Sternberg, C.M. (1945). "Pachycephalosauridae proposed for dome-headed dinosaurs, Stegoceras lambei, n. sp., described". Journal of Paleontology. 19 (5): 534–538. JSTOR 1299007.
- ^ Chapman, R.E.; Galton, P.M.; Sepkoski, J.J.; Wall, W.P. (1981). "A morphometric study of the cranium of the pachycephalosaurid dinosaur Stegoceras". Journal of Paleontology. 55 (3): 608–618. JSTOR 1304275.
- ^ Longrich, N.R.; Sankey, J. & Tanke, D. (2010). "Texacephale langstoni, a new genus of pachycephalosaurid (Dinosauria: Ornithischia) from the upper Campanian Aguja Formation, southern Texas, USA". Cretaceous Research. 31 (2): 274–284. Bibcode:2010CrRes..31..274L. doi:10.1016/j.cretres.2009.12.002.
- ^ Schott, R.K. (2011). Ontogeny, Diversity, and Systematics of Pachycephalosaur Dinosaurs from the Belly River Group of Alberta (M.Sc.). Department of Ecology and Evolutionary Biology, University of Toronto. p. 173.