Edmontosaurus regalis

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Edmontosaurus regalis
Temporal range: Late Cretaceous, 73–70  Ma
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Edmontosaurus annectens specimen.jpg
Holotype skeleton of Thespesius edmontoni, now thought to be a young E. regalis
Scientific classification OOjs UI icon edit-ltr.svg
Domain: Eukaryota
Kingdom: Animalia
Phylum: Chordata
Clade: Dinosauria
Clade: Ornithischia
Clade: Ornithopoda
Family: Hadrosauridae
Subfamily: Saurolophinae
Genus: Edmontosaurus
Species:
E. regalis
Binomial name
Edmontosaurus regalis
Synonyms
  • Trachodon avatusCope, 1871
  • Thespesius edmontoniGilmore, 1924
  • Anatosaurus edmontoni(Gilmore, 1924) Lull & Wright, 1942
  • Edmontosaurus edmontoni(Gilmore, 1924) Russell and Chamney, 1967
  • Thespesius edmontonensisGilmore, 1924 emend Olshevsky, 1991

Edmontosaurus regalis is a species of comb-crested hadrosaurid dinosaur. Fossils of E. regalis have been found in rocks of western North America that date from the late Campanian age of the Cretaceous Period 73 million years ago, but it may have possibly lived into the early Maastrichtian. [1]

Contents

E. regalis was one of the largest hadrosaurids, measuring up to 12 metres (39 ft) long and weighing around 4.0 metric tons (4.4 short tons). It is classified as a genus of saurolophine (or hadrosaurine) hadrosaurid, a member of the group of hadrosaurids that lacked large, hollow crests, and instead had smaller, solid crests or fleshy combs. [2] The distribution of E. regalis fossils suggests that it preferred coasts and coastal plains. It was a herbivore that could move on both two legs and four. Because it is known from several bone beds, E. regalis is thought to have lived in large groups. The wealth of fossils has allowed researchers to study its paleobiology in detail, including its brain, how it may have fed, and its injuries and pathologies.

Description

Scale diagram comparing E. regalis and E. annectens to a human Edmontosaurus scale.png
Scale diagram comparing E. regalis and E. annectens to a human

Edmontosaurus regalis is known from several fossil specimens. [3] [4] [5] [6] E. regalis was among the largest of hadrosaurids, as a fully grown adult could have been 9 metres (30 ft) long. Some of the larger specimens reached the range of 12 metres (39 ft) [7] to 13 metres (43 ft) long. [8] Its weight was on the order of 4.0 metric tons (4.4 short tons). [9] The type specimen of E. regalis, NMC  2288, is estimated as 9 to 12 metres (30 to 39 ft) long. [10] A 2022 study proposed that E. regalis may have been heavier than its generic relative, E. annectens, but not enough samples exist to provide a valid estimate and examination on its osteohistology and growth, so the results for E. regalis aren't statistically significant. [11]

The skull was roughly triangular in profile. [12] One specimen preserved a soft tissue crest or wattle on top of its head. [2] The beak was toothless, with both the upper and lower beaks being extended by keratinous material. [9] Its teeth were present only in the maxillae (upper cheeks) and dentaries (main bone of the lower jaw). [13] [14] They grew in columns, with an observed maximum of six in each and the number of columns varied based on the animal's size. [6] There were 51 to 53 columns per maxilla and 48 to 49 per dentary (teeth of the upper jaw being slightly narrower than those in the lower jaw). [12]

Life restoration Edmontosaurus BW.jpg
Life restoration

E. regalis had thirteen neck vertebrae, eighteen back vertebrae, nine hip vertebrae, and an unknown number of tail vertebrae. [12] The front legs were shorter and less heavily built than the back legs. Each hand had four fingers, but no thumb (first finger). The second, third, and fourth fingers were approximately the same length and unified in life within a fleshy covering. Although the second and third finger had hoof-like claws, these bones were also within the skin and not apparent from the outside. The little finger was separate from the other three and was much shorter. [15] Each foot had three toes, with no big toe or little toe. The toes had keratinous hoof-like tips. [6]

Discovery and history

Fossil skull ROM 801 Edmontosaurus regalis skull and jaws, Near Drumheller, Alberta, Canada, Late Cretaceous - Royal Ontario Museum - DSC00020.JPG
Fossil skull ROM 801

The first known fossil remains that may belong to Edmontosaurus regalis were named Trachodon cavatus in 1871 by Edward Drinker Cope. [16] The name is spelled in more recent sources as Trachodon avatus [7] or as Trachodon atavus. [9] [17] This species was assessed without comment as a synonym of Edmontosaurus regalis in two reviews, [9] [17] although T. atavus predates E. regalis by several decades. In 1874, Cope named (but did not describe) Agathaumas milo for a sacral vertebra and shin fragments from the late Maastrichtian-age Upper Cretaceous Laramie Formation of Colorado. [7] [18] [19] Later that same year, he described these bones under the name Hadrosaurus occidentalis. [7] [19] [20] Sadly, the bones are now lost to history. [19] As with Trachodon atavus, Agathaumas milo has been assigned without comment to Edmontosaurus regalis in two reviews, [9] [17] although predating E. regalis by several decades. Neither species has attracted much attention, as both are absent from Lull and Wright's 1942 monograph, for example. A third and obscure early species, Trachodon selwyni, described by Lawrence Lambe in 1902 for a lower jaw from what is now known as the Dinosaur Park Formation of Alberta, [21] was erroneously described by Glut (1997) as having been assigned to Edmontosaurus regalis by Lull and Wright. [7] It was not, instead being designated "of very doubtful validity." [22] More recent reviews of hadrosaurids have concurred. [9] [17]

The type specimen of E. regalis is NMC  2288, which consists of a skull, articulated vertebrae up to the sixth tail vertebra, ribs, partial hips, an upper arm bone, and most of a hind limb. It was discovered in 1912 by Levi Sternberg. The second specimen, paratype NMC 2289, consists of a skull and skeleton lacking the beak, most of the tail, and part of the feet. It was discovered in 1916 by George F. Sternberg. Both skeletons were found in the Horseshoe Canyon Formation (formerly the lower Edmonton Formation) along the Red Deer River of southern Alberta. [23] Thus, the Edmonton Formation lent Edmontosaurus its name. [24] The name Edmontosaurus regalis (meaning "regal," or, more loosely, "king-sized"), [24] was coined in 1917 by Lawrence Lambe. Lambe found that his new dinosaur compared best to specimens of " Diclonius mirabilis " (now assigned to Edmontosaurus annectens ) and drew attention to the size and robustness of Edmontosaurus regalis. [23] Initially, Lambe only described the skulls of the two skeletons, but returned to the genus in 1920 to describe the skeleton of NMC 2289. [3] The postcrania of the type specimen remains undescribed, still in its plaster jackets. [7]

Skull NHM R8927 at the Natural History Museum Edmontosaurus regalis skull.jpg
Skull NHM R8927 at the Natural History Museum

Two more species that would come to be included with Edmontosaurus regalis were named from Canadian remains in the 1920s, but both would initially be assigned to the dubious genus Thespesius . Gilmore named the first, Thespesius edmontoni, in 1924. T. edmontoni also came from the Horseshoe Canyon Formation. It was based on NMC 8399, another nearly complete skeleton lacking most of the tail. NMC 8399 was discovered on the Red Deer River in 1912 by a Sternberg party. [4] Its forelimbs, ossified tendons, and skin impressions were briefly described in 1913 and 1914 by Lambe, who at first thought it was an example of a species he'd named Trachodon marginatus, [25] but he changed his mind. [26] The specimen became the first dinosaur skeleton to be mounted for exhibition in a Canadian museum. Gilmore found that his new species compared closely to what he called Thespesius annectens , but left the two apart because of details of the arms and hands. He also noted that his species had more vertebrae than Marsh's in the back and neck, but proposed that Marsh was mistaken in assuming that the annectens specimens were complete in those regions. [4]

In 1926, Charles Mortram Sternberg named Thespesius saskatchewanensis for NMC 8509, which is a skull and partial skeleton from the Wood Mountain plateau of southern Saskatchewan. He had collected this specimen in 1921 from rocks that were assigned to the Lance Formation, [5] now the Frenchman Formation. [9] NMC 8509 included an almost complete skull, numerous vertebrae, partial shoulder and hip girdles, and partial legs. This represented the first substantial dinosaur specimen recovered from Saskatchewan. Sternberg opted to assign it to Thespesius because that was the only hadrosaurid genus known from the Lance Formation at the time. [5] T. saskatchewanensis was unusual because of its small size, estimated at 7 to 7.3 metres (23 to 24 ft) in length. [12]

Classification

Reconstruction of E. regalis Edmontosaurus regalis.PNG
Reconstruction of E. regalis
Most known complete Edmontosaurus skulls (E. regalis from left to upper middle) Edmontosaurus skulls.png
Most known complete Edmontosaurus skulls (E. regalis from left to upper middle)

The cladogram below follows an analysis from Godefroit et al. (2012). [27]

Paleobiology

Close up of tooth crowns Edmontosaurus regalis tooth crowns.png
Close up of tooth crowns

In a 2011 study, Campione and Evans recorded data from all known edmontosaur skulls and used it to plot a morphometric graph, comparing variable features of the skull with skull size. Their results showed that within Edmontosaurus regalis, many features previously used to classify additional species were directly correlated with skull size. Campione and Evans interpreted these results as strongly suggesting that the shape of E. regalis skulls changed dramatically as they grew. This has led to several apparent mistakes in past classification. The Campanian species Thespesius edmontoni, previously considered a synonym of E. annectens because of its small size and skull shape, is more likely a subadult specimen of E. regalis. [28] In a 2014 study, researchers proposed that E. regalis reached maturity at 10-15 years of age. [29] A preserved rhamphotheca present in specimen LACM 23502, housed in the Los Angeles County Museum, also indicates the beak of the related Edmontosaurus annectens was more hook-shaped and extensive than many illustrations in scientific and public media have previously depicted. Whether this was true of E. regalis as well is still unknown as of this time. [30] [31]

Extensive bone beds are known for Edmontosaurus regalis and such groupings of hadrosaurids are used to suggest that they were gregarious, living in herds. [9] Two quarries containing E. regalis remains were identified in a 2007 database of fossil bone beds, including ones in Alaska (Prince Creek Formation) and Alberta (Horseshoe Canyon Formation). [32]

Paleoecology

Horseshoe Canyon Formation near Drumheller. The dark bands are coal seams. Horseshoe Canyon Alberta Nov 1988.jpg
Horseshoe Canyon Formation near Drumheller. The dark bands are coal seams.

The Edmontonian land vertebrate age is defined by the first appearance of Edmontosaurus regalis in the fossil record. [33] Although sometimes reported as of exclusively the early Maastrichtian age, [34] the Horseshoe Canyon Formation was of somewhat longer duration. Deposition began approximately 73 million years ago, in the late Campanian, and ended between 68.0 and 67.6 million years ago. [35] Edmontosaurus regalis is known from the lowest of five units within the Horseshoe Canyon Formation, but is absent from at least the second to the top. [36]

Because of its wide distribution, which covers a distance from Alaska to Colorado and includes polar settings that would have had little light during a significant part of the year, Edmontosaurus regalis has been considered possibly migratory. A 2008 review of dinosaur migration studies by Phil R. Bell and Eric Snively proposed that E. regalis was capable of an annual 2,600 kilometres (1,600 mi) round-trip journey, provided it had the requisite metabolism and fat deposition rates. Such a trip would have required walking speeds of about 2 to 10 kilometres per hour (1 to 6 mph) and could have brought it from Alaska to Alberta. The possible migratory nature of E. regalis contrasts with many other dinosaurs, such as theropods, sauropods, and ankylosaurians, which Bell and Snively found were more likely to have overwintered. [37] [38] In contrast to Bell and Snively, Anusuya Chinsamy and colleagues concluded from a study of bone microstructure that polar edmontosaurs overwintered. [39]

Contemporary fauna

Reconstruction of the Tyrants Aisle tracksite, featuring an E. regalis herd and contemporary paleofauna Tyrants Aisle tracksite reconstruction.png
Reconstruction of the Tyrants Aisle tracksite, featuring an E. regalis herd and contemporary paleofauna

As many as three quarters of the dinosaur specimens from the badlands near Drumheller may pertain to Edmontosaurus regalis. [40] The Horseshoe Canyon Formation is interpreted as having a significant marine influence, due to the encroaching Western Interior Seaway. This shallow sea stretched from the Gulf of Mexico to the Arctic Ocean, covering the midsection of North America through much of the Cretaceous. [41] E. regalis shared this setting with fellow hadrosaurids Hypacrosaurus and Saurolophus , the parksosaurid Parksosaurus , the ceratopsids Montanoceratops , Anchiceratops , Arrhinoceratops , and Pachyrhinosaurus , the pachycephalosaurid Stegoceras , the ankylosaurid Euoplocephalus , the nodosaurid Edmontonia , the ornithomimids Ornithomimus and Struthiomimus , a variety of poorly known small theropods that included troodontids and dromaeosaurids, and the tyrannosaurid Albertosaurus . [34]

Edmontosaurus is found in coastal, near-marine settings, while Hypacrosaurus and Saurolophus are found in more continental lowlands. [42] Edmontosaurus and Saurolophus are not usually found together. [43] The typical edmontosaur habitat of this formation has been described as the back regions of bald cypress swamps and peat bogs on delta coasts. Pachyrhinosaurus also preferred this habitat to the floodplains dominated by Hypacrosaurus, Saurolophus, Anchiceratops, and Arrhinoceratops. [40] The Edmontonian-age coastal Pachyrhinosaurus-Edmontosaurus association is recognized as far north as Alaska. [44]

See also

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<i>Edmontosaurus</i> mummy SMF R 4036 Dinosaur fossil in Naturmuseum Senckenberg

The Edmontosaurus mummy SMF R 4036 is an exceptionally well-preserved dinosaur fossil in the collection of the Naturmuseum Senckenberg (SM) in Frankfurt am Main, Germany. Found in 1910 in Wyoming, United States, it is ascribed to the species Edmontosaurus annectens, a member of the Hadrosauridae. The fossil comprises a nearly complete skeleton that was found wrapped in impressions of its skin, a rare case of exceptional preservation for which the term "dinosaur mummy" has been used. Notably, the horny beak is preserved with this specimen. Plant remains found within the thorax cavity had been interpreted as stomach contents, although later research questioned this identification. The mummy's hands are wrapped in skin impression, which was interpreted as evidence for interdigital webbing and an aquatic lifestyle in hadrosaurids; this hypothesis, although universally accepted once, is now widely refused. SMF R 4036 is one of the four best preserved hadrosaurid mummies, and was the second to be discovered. The find was made by fossil hunter Charles Hazelius Sternberg and his sons, who sold their numerous finds to various museums in North America and Europe. Only two years earlier the Sternbergs had discovered the Edmontosaurus mummy AMNH 5060 in the same region, which is now on display at the American Museum of Natural History (AMNH) in New York City.

References

  1. Campbell, J. A.; Ryan, M. J.; Anderson, J. S. (2020). "A taphonomic analysis of a multitaxic bonebed from the St. Mary River Formation (uppermost Campanian to lowermost Maastrichtian) of Alberta, dominated by cf. Edmontosaurus regalis (Ornithischia: Hadrosauridae), with significant remains of Pachyrhinosaurus canadensis (Ornithischia: Ceratopsidae)". Canadian Journal of Earth Sciences. 57 (5): 617–629. Bibcode:2020CaJES..57..617C. doi:10.1139/cjes-2019-0089. S2CID   210287585.
  2. 1 2 Bell, P. R.; Fanti, F.; Currie, P. J.; Arbour, V.M. (2013). "A Mummified Duck-Billed Dinosaur with a Soft-Tissue Cock's Comb". Current Biology. 24 (1): 70–75. doi: 10.1016/j.cub.2013.11.008 . PMID   24332547.
  3. 1 2 Lambe, Lawrence M. (1920). The hadrosaur Edmontosaurus from the Upper Cretaceous of Alberta. Memoir. Vol. 120. Department of Mines, Geological Survey of Canada. pp. 1–79. ISBN   978-0-659-96553-0.
  4. 1 2 3 Gilmore, Charles W. (1924). A new species of hadrosaurian dinosaur from the Edmonton Formation (Cretaceous) of Alberta. Bulletin. Vol. 38. Department of Mines, Geological Survey of Canada. pp. 13–26.
  5. 1 2 3 Sternberg, Charles M. (1926). A new species of Thespesius from the Lance Formation of Saskatchewan. Bulletin. Vol. 44. Department of Mines, Geological Survey of Canada. pp. 77–84.
  6. 1 2 3 Lull, Richard Swann; Wright, Nelda E. (1942). Hadrosaurian Dinosaurs of North America. Geological Society of America Special Paper 40. Geological Society of America. pp. 50–93.
  7. 1 2 3 4 5 6 Glut, Donald F. (1997). "Edmontosaurus". Dinosaurs: The Encyclopedia . Jefferson, North Carolina: McFarland & Co. pp.  389–396. ISBN   978-0-89950-917-4.
  8. Lambert, David; the Diagram Group (1990). The Dinosaur Data Book . New York: Avon Books. p.  60. ISBN   978-0-380-75896-8.
  9. 1 2 3 4 5 6 7 8 Horner, John R.; Weishampel, David B.; Forster, Catherine A. (2004). "Hadrosauridae". In Weishampel, David B.; Dodson, Peter; Osmólska, Halszka (eds.). The Dinosauria (2nd ed.). Berkeley: University of California Press. pp.  438–463. ISBN   978-0-520-24209-8.
  10. Lull, Richard Swann; and Wright, Nelda E. (1942). Hadrosaurian Dinosaurs of North America. p. 225.
  11. Wosik, M.; Evans, D.C. (2022). "Osteohistological and taphonomic life-history assessment of Edmontosaurus annectens (Ornithischia: Hadrosauridae) from the Late Cretaceous (Maastrichtian) Ruth Mason dinosaur quarry, South Dakota, United States, with implication for ontogenetic segregation between juvenile and adult hadrosaurids". Journal of Anatomy. 241 (2): 272–296. doi:10.1111/joa.13679. PMC  9296034. PMID   35801524.
  12. 1 2 3 4 Lull, Richard Swann; and Wright, Nelda E. (1942). Hadrosaurian Dinosaurs of North America. pp. 151–164.
  13. Stanton Thomas, Kathryn J.; Carlson, Sandra J. (2004). "Microscale δ18O and δ13C isotopic analysis of an ontogenetic series of the hadrosaurid dinosaur Edmontosaurus: implications for physiology and ecology". Palaeogeography, Palaeoclimatology, Palaeoecology. 206 (2004): 257–287. Bibcode:2004PPP...206..257S. doi:10.1016/j.palaeo.2004.01.007.
  14. Erickson, Gregory M.; Krick, Brandon A.; Hamilton, Matthew; Bourne, Gerald R.; Norell, Mark A.; Lilleodden, Erica; Sawyer, W. Gregory. (2012). "Complex dental structure and wear biomechanics in hadrosaurid dinosaurs". Science. 338 (6103): 98–101. Bibcode:2012Sci...338...98E. doi:10.1126/science.1224495. PMID   23042891. S2CID   35186603.
  15. Lull, Richard Swann; and Wright, Nelda E. (1942). Hadrosaurian Dinosaurs of North America. pp. 98–110.
  16. Cope, Edward Drinker (1871). "Supplement to the synopsis of the extinct Batrachia and Reptilia of North America". Proceedings of the American Philosophical Society. 12 (86): 41–52.
  17. 1 2 3 4 Weishampel, David B.; Horner, Jack R. (1990). "Hadrosauridae". In Weishampel, David B.; Dodson, Peter; Osmólska, Halszka (eds.). The Dinosauria (1st ed.). Berkeley: University of California Press. pp. 534–561. ISBN   978-0-520-06727-1.
  18. Cope, Edward Drinker (1874). "Report on the stratigraphy and Pliocene vertebrate paleontology of northern Colorado". U.S. Geological and Geographical Survey of the Territories Annual Report. 1: 9–28.
  19. 1 2 3 Carpenter, Kenneth; Young, D. Bruce (2002). "Late Cretaceous dinosaurs from the Denver Basin, Colorado" (PDF). Rocky Mountain Geology. 37 (2): 237–254. Bibcode:2002RMGeo..37..237C. doi:10.2113/11.
  20. Cope, Edward Drinker (1874). "Report on the vertebrate paleontology of Colorado". U.S. Geological and Geographical Survey of the Territories Annual Report. 2: 429–454.
  21. Lambe, Lawrence M. (1902). "On Vertebrata of the mid-Cretaceous of the Northwest Territory. 2. New genera and species from the Belly River Series (mid-Cretaceous)". Contributions to Canadian Paleontology. 3: 25–81.
  22. Lull, Richard Swann; and Wright, Nelda E. (1942). Hadrosaurian Dinosaurs of North America. pp. 220–221.
  23. 1 2 Lambe, Lawrence M. (1917). "A new genus and species of crestless hadrosaur from the Edmonton Formation of Alberta" (pdf (entire volume, 18 mb)). The Ottawa Naturalist. 31 (7): 65–73. Retrieved 2009-03-08.
  24. 1 2 Creisler, Benjamin S. (2007). "Deciphering duckbills: a history in nomenclature". In Carpenter Kenneth (ed.). Horns and Beaks: Ceratopsian and Ornithopod Dinosaurs. Bloomington and Indianapolis: Indiana University Press. pp. 185–210. ISBN   978-0-253-34817-3.
  25. Lambe, Lawrence M. (1913). "The manus in a specimen of Trachodon from the Edmonton Formation of Alberta". The Ottawa Naturalist. 27: 21–25.
  26. Lambe, Lawrence M. (1914). "On the fore-limb of a carnivorous dinosaur from the Belly River Formation of Alberta, and a new genus of Ceratopsia from the same horizon, with remarks on the integument of some Cretaceous herbivorous dinosaurs". The Ottawa Naturalist. 27: 129–135.
  27. Godefroit, P.; Bolotsky, Y. L.; Lauters, P. (2012). ""Joger, Ulrich, ed. "A New Saurolophine Dinosaur from the Latest Cretaceous of Far Eastern Russia". PLOS ONE. 7 (5): e36849. Bibcode:2012PLoSO...736849G. doi: 10.1371/journal.pone.0036849 . PMC   3364265 . PMID   22666331.
  28. Campione, N. S. E.; Evans, D. C. (2011). "Cranial Growth and Variation in Edmontosaurs (Dinosauria: Hadrosauridae): Implications for Latest Cretaceous Megaherbivore Diversity in North America". PLOS ONE. 6 (9): e25186. Bibcode:2011PLoSO...625186C. doi: 10.1371/journal.pone.0025186 . PMC   3182183 . PMID   21969872.
  29. Vanderven, E.; Burns, M.E.; Currie, P.J. (2014). "Histologic growth dynamic study of Edmontosaurus regalis (Dinosauria: Hadrosauridae) from a bonebed assemblage of the Upper Cretaceous Horseshoe Canyon Formation, Edmonton, Alberta, Canada". Canadian Journal of Earth Sciences. 51 (11): 1023–1033. Bibcode:2014CaJES..51.1023V. doi:10.1139/cjes-2014-0064.
  30. "Enough with the "Duck-Billed Dinosaurs"".
  31. "Shovel-Beaked, Not Duck-Billed".
  32. Behrensmeyer, Anna K. (2007). "Evolution of Terrestrial Ecosystems Bonebed Database" (Excel spreadsheet). Bonebeds: Genesis, Analysis, and Paleobiological Significance. University of Chicago Press. Retrieved 2008-12-07.
  33. Sullivan, Robert M.; Lucas, Spencer G. (2006). "The Kirtlandian land-vertebrate "age" – faunal composition, temporal position and biostratigraphic correlation in the nonmarine Upper Cretaceous of western North America" (PDF). Late Cretaceous Vertebrates fvry and Science. New Mexico Museum of Natural History and Science Bulletin 35. Albuquerque, New Mexico. pp. 7–29.{{cite book}}: CS1 maint: location missing publisher (link)[ permanent dead link ]
  34. 1 2 Weishampel, David B.; Barrett, Paul M.; Coria, Rodolfo A.; Le Loueff, Jean; Xu Xing; Zhao Xijin; Sahni, Ashok; Gomani, Elizabeth M.P.; Noto, Christopher N. (2004). "Dinosaur distribution". In Weishampel, David B.; Dodson, Peter; Osmólska, Halszka (eds.). The Dinosauria (2nd ed.). Berkeley: University of California Press. pp.  517–606. ISBN   978-0-520-24209-8.
  35. Wu, X-C.; Brinkman, D.B.; Eberth, D.A.; Braman, D.R. (2007). "A new ceratopsid dinosaur (Ornithischia) from the uppermost Horseshoe Canyon Formation (upper Maastrichtian), Alberta, Canada". Canadian Journal of Earth Sciences. 44 (9): 1243–1265. Bibcode:2007CaJES..44.1243W. doi:10.1139/E07-011.
  36. Eberth, David A. (2002). "Review and comparison of Belly River Group and Edmonton Group stratigraphy and stratigraphic architecture in the southern Alberta Plains" (PDF). Canadian Society of Petroleum Geology Diamond Jubilee Convention, Programs and Abstracts. 117: (cd). Archived from the original (PDF) on 2007-11-13. Retrieved 2009-03-08.
  37. Bell, Phil R.; Snively, E. (2008). "Polar dinosaurs on parade: a review of dinosaur migration". Alcheringa. 32 (3): 271–284. Bibcode:2008Alch...32..271B. doi: 10.1080/03115510802096101 .
  38. Lloyd, Robin (2008-12-04). "Polar Dinosaurs Endured Cold Dark Winters". LiveScience.com. Imaginova. Retrieved 2008-12-11.
  39. Chinsamy, A.; Thomas, D. B.; Tumarkin-Deratzian, A. R.; Fiorillo, A. R. (2012). "Hadrosaurs were perennial polar residents". The Anatomical Record. online preprint (4): 610–614. doi: 10.1002/ar.22428 . PMID   22344791.
  40. 1 2 Russell, Dale A. (1989). An Odyssey in Time: Dinosaurs of North America. Minocqua, Wisconsin: NorthWord Press, Inc. pp. 170–171. ISBN   978-1-55971-038-1.
  41. Dodson, Peter (1996). The Horned Dinosaurs: A Natural History . Princeton: Princeton University Press. pp.  14–15. ISBN   978-0-691-05900-6.
  42. Russell, Dale A.; Chamney, T. P. (1967). "Notes on the biostratigraphy of dinosaurian and microfossil faunas in the Edmonton Formation (Cretaceous), Alberta". National Museum of Canada Natural History Papers. 35: 1–35.
  43. "City Site Was Dinosaur Dining Room". ScienceDaily. 2007-07-03. Retrieved 2008-12-07.
  44. Lehman, Thomas M. (2001). "Late Cretaceous dinosaur provinciality". In Tanke, Darren; Carpenter, Kenneth (eds.). Mesozoic Vertebrate Life. Bloomington and Indianapolis: Indiana University Press. pp.  310–328. ISBN   978-0-253-33907-2.