Centrosaurinae (from the Greek, meaning "pointed lizards") is a subfamily of ceratopsid, a group of large quadrupedal ornithischian dinosaur. Centrosaurine fossil remains are known primarily from the northern region of Laramidia (modern day Alberta, Montana, and Alaska) but isolated taxa have been found in China and Utah as well.[3]
| Centrosaurines Temporal range: Late Cretaceous,
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| Centrosaurus "nasicornus" skeleton, Palaeontological Museum Munich | |
Scientific classification 
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| Domain: | Eukaryota |
| Kingdom: | Animalia |
| Phylum: | Chordata |
| Clade: | Dinosauria |
| Clade: | †Ornithischia |
| Clade: | †Neornithischia |
| Clade: | †Ceratopsia |
| Family: | †Ceratopsidae |
| Subfamily: | †Centrosaurinae Lambe, 1915 |
| Type species | |
| †Centrosaurus apertus Lambe, 1904
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| Subgroups | |
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| Synonyms | |
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Defining features of centrosaurines include a large nasal horn, short supratemporal horns, and an ornamented frill projecting from the back of the skull.[4] With the exception of Centrosaurus apertus, all adult centrosaurines have spike-like ornaments midway up the skull.[5] Morphometric analysis shows that centrosaurines differ from other ceratopsian groups in skull, snout, and frill shapes.[6] There is evidence to suggest that male centrosaurines had an extended period of adolescence, and sexual ornamentation did not appear until adulthood.[4]
Centrosaurinae was named by paleontologist Lawrence Lambe in 1915, with Centrosaurus as the type genus. The centrosaurines are further divided into three tribes: the Nasutoceratopsini, the Centrosaurini, and the Pachyrhinosaurini by Ryan et al (2016).[7] Nasutoceratopsins are defined as centrosaurines closer to Nasutoceratops titusi than to Centrosaurus apertus and centrosaurins are defined as centrosaurines (more specifically eucentrosaurans) closer to Centrosaurus apertus than to Pachyrhinosaurus canadensis. Until 2016, the only division used was Pachyrhinosaurini, which is defined as centrosaurines closer to Pachyrhinosaurus canadensis than to Centrosaurus apertus.
Classification
editThe classification of centrosaurines and the relationships among the various species is complicated by a wide degree of variation between individuals and growth stages. Some features that have traditionally been used to classify these dinosaurs, like the number and arrangement of frill ornaments or spikes, have been discovered to be more variable than previously thought. For example, the cladogram presented below follows a 2016 phylogenetic analysis by Chiba et al. (2017).[8] These authors treated the species Rubeosaurus ovatus as distinct from Styracosaurus albertensis, and recovered several distinct clades within Centrosaurini, which together formed a sister group to the Pachyrhinosaurini:
| Centrosaurinae |
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However, subsequent studies have cast doubt on the usefulness of minor variations in frill spike arrangement for classifying centrosaurines. In particular, large sample sizes of the species Centrosaurus apertus and Styracosaurus albertensis have shown a higher than predicted amount of variation. In 2020, Holmes et al. explored what the effect of recognizing such diversity would have on centrosaur classification. They used the same data as Chiba et al.'s 2017 study, but treated Rubeosaurus as a synonym of Styracosaurus, dropping it from their taxon list. The resulting cladogram (below) found Centrosaurini as a polytomy, a grouping with no discernable sister group relationships within it. The authors concluded that this meant the variation present within these species made it difficult to find any real resolution among them, and may even provide support for the hypothesis that centrosaurines evolved primarily via anagenesis (a single lineage changing through time) rather than cladogenesis (multiple branching lineages with shared common ancestors).[9]
| Centrosaurinae |
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Pachyrhinosaurini was defined in 2012 by Fiorillo & Tykoski. It was defined as all centrosaurine ceratopsids more closely related to Pachyrhinosaurus canadensis than to Centrosaurus apertus. It was defined during the description of Pachyrhinosaurus perotorum, a species from Alaska.[10] The substituent clade Pachyrostra, compromising centrosaurs with bossed instead of horned noses, is defined as "the least inclusive clade including both Pachyrhinosaurus canadensis and Achelousaurus horneri.[11]
Biogeography
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Centrosaurine fossils have mostly been found in Western North America (Alberta, Montana, and Alaska).[3] In the United States, two taxa, Diabloceratops and Machairoceratops, have been found as far south as Utah. Yehuecauhceratops, a nasutoceratopsin from Coahuila, Mexico, is the southernmost occurrence of a centrosaurine in North America.[3] No centrosaurine fossils had been uncovered outside Western North America until the 2010 discovery of Sinoceratops in the Shandong Province of China.[12] However, some authors question the placement of Sinoceratops within Centrosaurinae. All other Late Cretaceous dinosaur groups from North America have also been found in Asia, so the initial absence of Asian centrosaurines had been surprising.[12] The current evidence suggests that Centrosaurinae originated in Laramidia 90-80 million years ago,[3] with the discovery of the oldest known centrosaurine, Menefeeceratops further proving this.[13][1] This means Sinoceratops would have migrated to China from North America.[7] Some hypothesize that centrosaurines originated in southern Laramidia and later radiated north.[14]
Body size
editCompared to their sister group, Chasmosaurinae, centrosaurines are relatively small. The primitive Sinoceratops is an exception, with an estimated skull length of 180 centimetres (71 in).[12] By contrast, the skull length of Albertoceratops was more typical for this group at only 67 centimetres (26 in).[5] In general, centrosaurines were about the size of a rhinoceros with body lengths ranging from 2.5–8 metres (8.2–26.2 ft).[15]
Reproduction
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Possible neonate sized centrosaurine fossils have been documented in the scientific literature.[16] Research indicates that centrosaurines did not achieve fully developed mating signals until nearly fully grown.[17][4] Scott D. Sampson found commonality between the slow growth of mating signals in centrosaurines and the extended adolescence of animals whose social structures are ranked hierarchies founded on age-related differences.[17] In these sorts of groups, young males are typically sexually mature for several years before actually beginning to breed, when their mating signals are most fully developed.[18] Females, by contrast, do not have such an extended adolescence.[18]
See also
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Footnotes
edit- ^ a b Dalman, Sebastian G.; Lucas, Spencer G.; Jasinki, Steven G.; Lichtig, Asher J.; Dodson, Peter (2021). "The oldest centrosaurine: a new ceratopsid dinosaur (Dinosauria: Ceratopsidae) from the Allison Member of the Menefee Formation (Upper Cretaceous, early Campanian), northwestern New Mexico, USA". PalZ. 95 (2): 291–335. doi:10.1007/s12542-021-00555-w. ISSN 0031-0220. S2CID 234351502.
- ^ Fiorillo, Anthony R. and Tykoski, Ronald S. (2012). "A new Maastrichtian species of the centrosaurine ceratopsid Pachyrhinosaurus from the North Slope (Prince Creek Formation: Maastrichtian) of Alaska". Acta Palaeontologica Polonica. 57 (3): 561–573. doi:10.4202/app.2011.0033.
- ^ a b c d Sampson, Scott D.; Lund, Eric K.; Loewen, Mark A.; Farke, Andrew A.; Clayton, Katherine E. (2013-09-07). "A remarkable short-snouted horned dinosaur from the Late Cretaceous (late Campanian) of southern Laramidia". Proc. R. Soc. B. 280 (1766): 20131186. doi:10.1098/rspb.2013.1186. ISSN 0962-8452. PMC 3730592. PMID 23864598.
- ^ a b c Sampson, Scott D.; Ryan, Michael J.; Tanke, Darren H. (1997-11-01). "Craniofacial ontogeny in centrosaurine dinosaurs (Ornithischia: Ceratopsidae): taxonomic and behavioral implications". Zoological Journal of the Linnean Society. 121 (3): 293–337. doi:10.1111/j.1096-3642.1997.tb00340.x. ISSN 0024-4082.
- ^ a b Ryan, Michael J. (2007-03-01). "A new basal centrosaurine ceratopsid from the oldman formation, southeastern alberta". Journal of Paleontology. 81 (2): 376–396. doi:10.1666/0022-3360(2007)81[376:ANBCCF]2.0.CO;2. ISSN 0022-3360. S2CID 130607301.
- ^ Maiorino, Leonardo; Farke, Andrew A; Kotsakis, Tassos; Piras, Paolo (2017). "Macroevolutionary patterns in cranial and lower jaw shape of ceratopsian dinosaurs (Dinosauria, Ornithischia): phylogeny, morphological integration, and evolutionary rates" (PDF). Evolutionary Ecology Research. 18: 123–167.
- ^ a b Ryan, Michael J.; Holmes, Robert; Mallon, Jordan; Loewen, Mark; Evans, David C. (2016-10-27). "A basal ceratopsid (Centrosaurinae: Nasutoceratopsini) from the Oldman Formation (Campanian) of Alberta, Canada". Canadian Journal of Earth Sciences. 54 (1): 1–14. doi:10.1139/cjes-2016-0110. ISSN 0008-4077.
- ^ Kentaro Chiba; Michael J. Ryan; Federico Fanti; Mark A. Loewen; David C. Evans (2018). "New material and systematic re-evaluation of Medusaceratops lokii (Dinosauria, Ceratopsidae) from the Judith River Formation (Campanian, Montana)". Journal of Paleontology. 92 (2): 272–288. doi:10.1017/jpa.2017.62. S2CID 134031275.
- ^ Holmes RB, Persons WS, Rupal, BS, Qureshi, AJ, Currie PJ (2020). "Morphological variation and asymmetrical development in the skull of Styracosaurus albertensis". Cretaceous Research. 107: 104308. doi:10.1016/j.cretres.2019.104308. S2CID 210260909.
- ^ Fiorillo, Anthony R. & Gangloff, Roland A. (2001). "Theropod teeth from the Prince Creek Formation (Cretaceous) of northern Alaska, with speculations on Arctic dinosaur paleoecology". Journal of Vertebrate Paleontology. 20 (4): 675–682. doi:10.1671/0272-4634(2000)020[0675:TTFTPC]2.0.CO;2. S2CID 130766946.
- ^ Madzia, Daniel; Arbour, Victoria M.; Boyd, Clint A.; Farke, Andrew A.; Cruzado-Caballero, Penélope; Evans, David C. (2021-12-09). "The phylogenetic nomenclature of ornithischian dinosaurs". PeerJ. 9: e12362. doi:10.7717/peerj.12362. ISSN 2167-8359. PMC 8667728. PMID 34966571.
- ^ a b c Xu, Xing; Wang, KeBai; Zhao, XiJin; Li, DunJing (2010-06-01). "First ceratopsid dinosaur from China and its biogeographical implications". Chinese Science Bulletin. 55 (16): 1631–1635. Bibcode:2010ChSBu..55.1631X. doi:10.1007/s11434-009-3614-5. ISSN 1001-6538. S2CID 128972108.
- ^ Williamson, TE (1997). "A new Late Cretaceous (early Campanian) vertebrate fauna from the Allison Member, Menefee Formation, San Juan Basin, New Mexico". In Lucas, SG; Estep, JW; Williamson, TE; Morgan, GS (eds.). New Mexico's Fossil Record 1. Albuquerque: New Mexico Museum of Natural History and Science Bulletin 11. pp. 51–59. Retrieved 21 April 2021..
- ^ Lund, Eric K.; O’Connor, Patrick M.; Loewen, Mark A.; Jinnah, Zubair A. (2016-05-18). "A New Centrosaurine Ceratopsid, Machairoceratops cronusi gen et sp. nov., from the Upper Sand Member of the Wahweap Formation (Middle Campanian), Southern Utah". PLOS ONE. 11 (5): e0154403. Bibcode:2016PLoSO..1154403L. doi:10.1371/journal.pone.0154403. ISSN 1932-6203. PMC 4871575. PMID 27192148.
- ^ Rey, Luis V. (2007). Dinosaurs : the most complete, up-to-date encyclopedia for dinosaur lovers of all ages. Random House. ISBN 9780375824197. OCLC 930042495.
- ^ "Abstract," Tanke and Brett-Surman (2001). Page 207.
- ^ a b "Retarded Growth of Mating Signals," Sampson (2001); page 270.
- ^ a b "Sociological Correlates in Extant Vertebrates," Sampson (2001); page 265.
References
edit- Sampson, S. D. (1995b). "Two new horned dinosaurs from the Upper Cretaceous Two Medicine Formation of Montana; with a phylogenetic analysis of the Centrosaurinae (Ornithischia: Ceratopsidae)". Journal of Vertebrate Paleontology. 15 (4): 743–760. doi:10.1080/02724634.1995.10011259.
- Sampson, S. D., 2001, Speculations on the socioecology of Ceratopsid dinosaurs (Orinthischia: Neoceratopsia): In: Mesozoic Vertebrate Life, edited by Tanke, D. H., and Carpenter, K., Indiana University Press, pp. 263–276.
- Tanke, D.H. and Brett-Surman, M.K. 2001. Evidence of Hatchling and Nestling-Size Hadrosaurs (Reptilia:Ornithischia) from Dinosaur Provincial Park (Dinosaur Park Formation: Campanian), Alberta, Canada. pp. 206–218. In: Mesozoic Vertebrate Life—New Research Inspired by the Paleontology of Philip J. Currie. Edited by D.H. Tanke and K. Carpenter. Indiana University Press: Bloomington. xviii + 577 pp.