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.2020 May 6;15(5):e0232410.
doi: 10.1371/journal.pone.0232410. eCollection 2020.

Re-examination of the cranial osteology of the Arctic Alaskan hadrosaurine with implications for its taxonomic status

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Re-examination of the cranial osteology of the Arctic Alaskan hadrosaurine with implications for its taxonomic status

Ryuji Takasaki et al. PLoS One..

Abstract

Hadrosaurid fossils from the Liscomb Bonebed (Prince Creek Formation, North Slope, Alaska) were the first dinosaur bones discovered from the Arctic. While the Prince Creek Formation hadrosaurids were long identified as Edmontosaurus, a member of the sub-clade Hadrosaurinae, they were recently assigned to a newly-erected taxon, Ugrunaaluk kuukpikensis. However, taxonomic status of the new taxon is ambiguous largely due to the immature nature of the specimens upon which it was based. Here we reexamine cranial elements of the Prince Creek Formation hadrosaurine in order to solve its taxonomic uncertainties. The Prince Creek Formation hadrosaurine possesses a short dorsolateral process of the laterosphenoid, one of the diagnostic characters of Edmontosaurus. The Prince Creek Formation hadrosaurine also shows affinity to Edmontosaurus regalis in the presence of a horizontal shelf of the jugal. Our morphological comparisons with other North American Edmontosaurus specimens and our phylogenetic analyses demonstrate that the Prince Creek Formation hadrosaurine should be re-assigned to Edmontosaurus. Because the Prince Creek Formation Edmontosaurus shows differences with lower latitude Edmontosaurus in a dorsoventrally short maxilla, presence of a secondary ridge on the dentary teeth, and the absence of the transverse ridge between basipterygoid processes of the basisphenoid, we consider that the Prince Creek Formation Edmontosaurus should be regarded as Edmontosaurus sp. until further discoveries of mature hadrosaurines from the Prince Creek Formation Bonebed and/or equivalently juvenile Edmontosaurus specimens from the lower latitudes allow direct comparisons. The retention of the Prince Creek Formation hadrosaurine as Edmontosaurus re-establishes a significant latitudinal distribution for this taxon. Despite the large latitudinal distribution of the taxon, the morphological disparity of Edmontosaurus is small within Hadrosaurinae. The small morphological disparity may be related to the relatively low latitudinal temperature gradient during the latest Cretaceous compared to present day, a gradient which might not have imposed significant pressure for much morphological adaptations across a broad latitudinal range.

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Conflict of interest statement

The authors have declared that no competing interests exist.

Figures

Fig 1
Fig 1
Premaxillae of the PCF hadrosaurine (A-F). DMNH 22716, partial left and right premaxillae in left lateral (A), dorsal (B), and anterior (C) views. UAMES 12995, cast of a partial right premaxilla in right lateral (D), anterior (E), and dorsal (F) views. Premaxillae of immatureEdmontosaurus annectens ROM 53525(G), matureEdmontosaurus annectens ROM 64076 (H),Edmontosaurus regalis FMNH P15004 (I),Prosaurolophus maximus CMN 2870 (J),Brachylophosaurus canadensis CMN 8893 (K), andGryposaurus notabilis CMN 2278 (L) in dorsal views.
Fig 2
Fig 2
Cast of left maxilla (UAMES 4250) in lateral (A) and medial (B) views. (C) Height-length relationships of hadrosaurine maxillae, demonstrating negative allometry among Edmontosaurini.
Fig 3
Fig 3
Cast of left nasal (UAMES 4940) in lateral (A) and medial (B) views. Right prefrontal (DMNH 22972) in lateral (C), medial (D), and posterior (E) views. Casts of left (UAMES 4245; F-H) and right (UAMES 4254; I-K) lacrimals the PCF hadrosaurine in lateral (F, I), posterior (G, J), and medial (H, K) views. Isolated right lacrimals of a large (ROM 64076; L, M) and a small (ROM 53512; N, O)Edmontosaurus annectens in lateral (L, N) and medial (M, O) views.
Fig 4
Fig 4
Cast of right jugal of the PCF hadrosaurine (UAMES 4187) in lateral (A) and medial (B) views. Anterior process of left jugal ofEdmontosaurus annectens (C: ROM 53518; D: DMNH EPV. 95220; E: DMNH EPV. 130653) in medial view, demonstrating intraspecific variation of the angle between the palatine process and the posterior margin of the maxilla contact surface. Left quadratojugal (DMNH 2014-12-661) in lateral (F), medial (G), and posterior (H) views. Right quadrate (DMNH 21044) in lateral (I), anterior (J), medial (K), and posterior (L) views.
Fig 5
Fig 5
Cast of left squamosal (UAMES 12266) in lateral (A), dorsal (B), and posterior (C) views. Right postorbital (DMNH 2014-12-486) in lateral (D), anterior (E), and medial (F) views. Parietal (DMNH 2014-12-265) in dorsal (G) and ventral (H) views. Left frontal (DMNH 2014-12-635) in dorsal (I), ventral (J), lateral (K), and medial (L) views.
Fig 6
Fig 6
Cast of left pterygoid (UAMES 4215) in lateral (A) and medial (B) views. Right ectopterygoid (DMNH 2014-12-492) in lateral (C) and medial (D) views. Cast of left palatine (UAMES 4257) in lateral (E) and medial (F) views. Cast of right laterosphenoid of the PCF hadrosaurine (UAMES 4352) in lateral (G) and medial (H) views. Laterosphenoids ofEdmontosaurus annectens (I; ROM 53507),Hypacrosaurus stebingeri (J; USNM 11893), andEolambia caroljonesa (K; CEUM 34366) in lateral view.
Fig 7
Fig 7
Cast of left prootic (UAMES 4357) in lateral (A) and medial (B) views. Cast of left exoccipital (UAMES 4263) in lateral (C) and anterior (D) views. Supraoccipital (DMNH 22807) in dorsal (E), right lateral (F), anterior (G), and posterodorsal (H) views. Cast of basisphenoid (UAMES 4301) in left lateral (J), dorsal (K), anterior (L), and ventral (M) views. Cast of basioccipital (UAMES 34723) in left lateral (N), dorsal (O), anterior (P), and ventral (Q) views.
Fig 8
Fig 8
Cast of a partial predentary (UAMES 4437) in dorsal (A), ventral (B), and anterior (C) views. Right dentary (DMNH 2014-12-531) in lateral (D), dorsal (E), and medial (F) views. Left surangular (DMNH 2014-12-456) in lateral (G), medial (H), and dorsal (I) views.
Fig 9
Fig 9
Maxillary teeth (DMNH 22718) in labial (A) and lingual (B) views. Dentary teeth (DMNH 22851) in lingual view (C). Isolated dentary tooth (DMNH 22338) in lingual (D) and mesial (E) views. Close-up of the marginal denticles of the dentary tooth (F).
Fig 10
Fig 10
(A) Strict consensus tree of the MPTs obtained from the first phylogenetic analysis which excludes the two immatureEdmontosaurus annectens OTUs. Numbers above each branch represent bootstrap values and those below the branch represent Bremer decay values. Bootstrap values below 20 and Bremer decay values below 1 are not shown. The polytomy consisting of the PCF hadrosaurine +Edmontosaurus annectens +Edmontosaurus regalis is the result of the two conflicting topologies shown in the small box. (B) A simplified strict consensus tree of MPTs obtained from the second phylogenetic analysis which incorporated two juvenileEdmontosaurus annectens OTUs, showing relationship within Hadrosaurinae. The polytomy consisting of the PCF hadrosaurine +Edmontosaurus annectens (including immature OTUs) +Edmontosaurus regalis is the result of the three conflicting topologies shown in the bottom box.
Fig 11
Fig 11. Morphospace of hadrosaurines recovered from the principal coordinate analysis using the phylogenetic cranial characters.
Abbreviations:Ag:Acristavus gagslarsoni,Bc:Brachylophosaurus canadensis,Ea:Edmontosaurus annectens,Er:Edmontosaurus regalis,Gl:Gryposaurus latidens,Gm:Gryposaurus monumentensis,Gn:Gryposaurus notabilis,Hf:Hadrosaurus foulkii,Kj:Kamuysaurus japonicus,Km:Kerberosaurus manakini,Kn:Kritosaurus navajovius,La:Lophorhothon atopus,Ly:Laiyangosaurus youngi,Mp:Maiasaura peeblesorum,Pb:Probrachylophosaurus bergei,Pm:Prosaurolophus maximus,Rc:Rhinorex condrupus,Sa:Saurolophus angustirostris,Sg:Shantungosaurus giganteus,Sk:Secernosaurus koerneri,So:Saurolophus osborni,Wd:Wulagasaurus dongi.
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