Elsevier

Cretaceous Research

Volume 49, May 2014, Pages 163-171
Cretaceous Research

Tyrannosaurid teeth from the Lomas Coloradas Formation, Cabullona Group (Upper Cretaceous) Sonora, México

https://doi.org/10.1016/j.cretres.2014.02.018Get rights and content

Highlights

  • Six unknown isolated theropod teeth were collected in the state of Sonora, Mexico.

  • Morphological and statistical analyses assigned the specimens to the Tyrannosauridae.

  • The discriminant function analysis classified four of the six teeth as Tyrannosaurus.

  • These specimens represent the most southern record of this genus in North America.

Abstract

The Lomas Coloradas Formation (Cabullona Group, Upper Cretaceous) in the state of Sonora, Mexico, has yielded a great diversity of continental vertebrates, especially dinosaurs. In this study we describe, analyze and illustrate six theropod teeth (ERNO specimens) that were found isolated and surface collected. Identification of the specimens is based upon the methodology provided by Smith (2005), Smith et al. (2007) and Smith et al. (2005). The results showed that the ERNO teeth are comparable to those of tyrannosaurid dinosaurs and some of them probably correspond to a new taxon. Their referral to the Tyrannosauridae family is supported by the presence of semi-conical, laterally compressed crowns with an ovoid cross-sectional base; slightly offset carinae with chisel-shaped denticles that are wider labio-lingually than longer proximo-distally; and the presence of enamel wrinkles at the base of some denticles on the labial surface. These wrinkles are not prominent adjacent to the serrations but they take the form of high relief deep enamel bands across the labial and lingual crown faces. Statistical principal component analysis (PCA) and discriminant function analysis (DFA) corroborated the taxonomically assignation of these teeth into this family. Particularly, the DFA analysis yielded very interesting results. This analysis classified ERNO 8549, 8550, 8551 and 8552 specimens as belonging to Tyrannosaurus, so they represent the most southern record of this genus in Western North America. Finally, the misclassification of ERNO 005 and ERNO 006 specimens remains puzzling. It probably was the result of the presence of juvenile individuals.

Introduction

Tyrannosaurids are one of the best-represented clades of large bodied theropods in the fossil record. During late Campanian the high diversity of tyrannosaurids on western North America represents the evolutionary radiation of a successful predatory morphotype that culminated with the apparition of Tyrannosaurus rex by the end of the Cretaceous period (Currie, 2003, Holtz, 2004, Brusatte et al., 2009, Carr et al., 2011; Brusatte et al., 2010; Loewen et al., 2013). Their fossils have a widespread occurrence ranging from the North Slope of Alaska (Brouwers et al., 1987, Clemens and Nelms, 1993, Rich et al., 1997) south to Coahuila Province of Mexico (Hernández-Rivera, 1997). However the bulk of articulated skeletal remains have been collected from Alberta (Cope, 1892, Lambe, 1902, Lambe, 1914, Lambe, 1917), Montana (Cope, 1876, Osborn, 1905, Osborn, 1912, Horner et al., 1992), Wyoming (Osborn, 1905, Osborn, 1912) and recently from Utah (Carr et al., 2011, Loewen et al., 2013). Tyrannosaurid fossils to the north and south of those regions tend to consist of isolated bones and teeth (e.g., Brouwers et al., 1987).

Tyrannosaurid tooth remains have been reported by Leidy since 1856. The dentition inside this group is markedly heterodont (Holtz, 1994, Holtz, 1996, Holtz, 2000, Farlow et al., 1991, Smith, 2005). Tyrannosaurid crowns correspond to semi-conical structures made up of stacked dentine cones with a thin external layer of enamel (Abler, 1992). Premaxillary tooth have D-shaped bases in cross section and have two serrated ridges – also known as carinae – located on the lingual side. Maxillary and dentary teeth are more laterally compressed and less recurved than in other theropods. These teeth have a round to ovoid cross-sectional base and stout saddle or chisel-shaped serrations on the mesial and distal margins of the tooth crown (Sankey, 2001, Samman et al., 2005). The carinae are slightly offset from the rostral and caudal margins of the tooth, especially in more robust teeth than in slender ones (Holtz, 2004). Sometimes the serrations are angled towards the apex of the tooth and are generally aligned along the carinae that curve lingually (Smith and Dodson, 2003). Distinct enamel wrinkles and bands are present at the denticle bases and across the labial and lingual surfaces (Brusatte et al., 2007).

Tyrannosaurid denticles on the maxillary and dentary teeth have additional characteristics: they are larger and more widely spaced than in other theropods (Farlow et al., 1991); the mesial and distal serrations are equivalent in size (Chandler, 1990); they are wider labially–lingually than they are long proximo-distally; generally they decrease in size towards the base and apex of the tooth; they possess sharp ridges of enamel along the midline and they are smaller relative to tooth length in larger individuals, but are larger in basal diameter and height (Samman et al., 2005, Chandler, 1990, Currie et al., 1990).

In this work we described and analyze six unknown theropod teeth that were found isolated and surface collected in the Lomas Coloradas Formation of the Cabullona Group (Upper Cretaceous) in northeastern Sonora, Mexico. This formation has yielded a great diversity of continental vertebrates, especially dinosaurs.

Section snippets

Geological setting

The teeth described in this study were collected from the upper part of the Lomas Coloradas Formation (Taliaferro, 1933). This formation is the uppermost unit of the 2.5-km-thick Cabullona Group (Taliaferro, 1933, González-León and Lawton, 1995) that crop out in northeastern Sonora (Fig. 1). The Cabullona Group composed from base upwards of the Corral de Enmedio Formation, Camas Sandstone, Packard Shale and Lomas Coloradas Formation represent fluvial, lacustrine and deltaic deposits, while the

Material and methods

All specimens described and discussed in this paper are housed at the paleontological collection of the Estación Regional del Noroeste (ERNO) in Sonora, Mexico. To classify qualitatively the ERNO specimens to a bone origin, we follow Samman et al. (2005) methodology for the different types of teeth that can be found in a jaw. The teeth were morphologically described and then a series of statistical analyses were run to assess the effectiveness in correlating morphological characters with

Systematic palaeontology

  • Order Saurischia Seeley, 1887

  • Suborder Theropoda Marsh, 1881

  • Family Tyrannosauridae Osborn, 1905

  • Material. Six isolated teeth (ERNO 8549, ERNO 8550, ERNO 8551, ERNO 8552, ERNO 005 and ERNO 006).

  • Locality and horizon. Lomas Coloradas Formation, Cabullona Group; age: Maastrichtian.

  • Measurements. Table 1

  • Description. Specimens corresponded to shed crowns that have different degrees of preservation ranging from medium to poorly preserve. The carinae in these teeth are slightly offset from the mesial and

Morphology

The specimens described in this paper possess a series of characteristics that match the ones present in tyrannosaurid teeth: they correspond to semi-conical shed crowns that are laterally compressed and have an ovoid cross-sectional base. Two of the specimens correspond to incrassate teeth while the remaining are ziphodonts (Brusatte et al., 2010; Loewen et al., 2013). They have slightly offset carinae with chisel-shaped denticles that are wider labio-lingually than longer proximo-distally and

Conclusions

Isolated theropod teeth are common fossils in Mesozoic rocks and are frequently used to extend the temporal and geographic ranges of taxa known for more complete specimens (Brusatte et al., 2007). It has been observed that theropod teeth display a series of qualitative and quantitative characters that could be used as an important discrimination source for taxa recognition.

In this article, six unknown isolated teeth that were collected in the Lomas Coloradas Formation, Cabullona Group (Upper

Acknowledgments

The authors want to thank Dr. Steve Brusatte and an anonymous reviewer for their detailed and thoughtful reviews that greatly improved the preparation of this manuscript.

References (58)

  • R.E. Molnar et al.

    The Jordan Theropod (Maastrichtian, Montana, U.S.A.) Referred to the Genus Aublysodon

    Geobios

    (1989)
  • W.L. Abler

    The serrated teeth of tyrannosaurid dinosaurs, and biting structures in other animals

    Paleobiology

    (1992)
  • R.B.J. Benson et al.

    A new clade of archaic large-bodied predatory dinosaurs (Theropoda: Allosauroidea) that survived to the latest Mesozoic

    Naturwissenschaften

    (2010)
  • E.M. Brouwers et al.

    Dinosaurs on the North Slope, Alaska: high latitude, Latest Cretaceous environments

    Science

    (1987)
  • S.L. Brusatte et al.

    The systematic utility of theropod enamel wrinkles

    Journal of Vertebrate Paleontology

    (2007)
  • S.L. Brusatte et al.

    A long-snouted multihorned tyrannosaurid from the Late Cretaceous of Mongolia

    Proceedings of the National Academy of Sciences

    (2009)
  • S.L. Brusatte et al.

    Tyrannosaur Paleobiology: New Research on Ancient Exemplar Organisms

    Science

    (2010)
  • T.D. Carr

    Craniofacial ontogeny in Tyrannosauridae (Dinosauria, Coelurosauria)

    Journal of Vertebrate Paleontology

    (1999)
  • T.D. Carr et al.

    Evidence for high taxonomic and morphologic tyrannosauroid diversity in the Late Cretaceous (Late Campanian) of the American Southwest and a new short-skulled tyrannosaurid from the Kaiparowitz formation of Utah

    Naturwissenschaften

    (2011)
  • T.D. Carr et al.

    A Review of Tyrannosauridae (Dinosauria, Coelurosauria) From New Mexico

  • C.L. Chandler

    Taxonomic and functional significance of serrated tooth morphology in Theropod dinosaurs

    (1990)
  • A.J. Charig et al.

    Baryonyx, a remarkable new theropod dinosaur

    Nature

    (1986)
  • W.A. Clemens et al.

    Paleoecological implications of Alaskan terrestrial vertebrate fauna in latest Cretaceous time at high paleolatitudes

    Geology

    (1993)
  • E.D. Cope

    Description of some vertebrate remains from the Fort Union beds of Montana

    Proceedings of the Academy of Natural Sciences of Philadelphia

    (1876)
  • E.D. Cope

    On the skull of the dinosaurian Laelaps incrassatus Cope

    American Philosophical Society

    (1892)
  • R.A. Coria et al.

    A new charcarodontosaurid (Dinosauria, Theropoda) from the upper Cretaceous of Argentina

    Geodiversitas

    (2006)
  • R.A. Coria et al.

    A new giant carnivorous dinosaur from the Cretaceous of Patagonia

    Nature

    (1995)
  • P.J. Currie

    Cranial anatomy of tyrannosaurid dinosaurs from the Late Cretaceous of Alberta, Canada

    Acta Paleontologica Polonica

    (2003)
  • P.J. Currie et al.
  • P.J. Currie et al.
  • J.O. Farlow et al.

    Size, shape and serration density of theropod dinosaur lateral teeth

    Modern Geology

    (1991)
  • C. González-León et al.

    Stratigraphy, depositional environments and origin of the Late Cretaceous Cabullona basin, northeastern Sonora, Mexico

    Geological Society of America, Special Paper

    (1995)
  • R. Hernández-Rivera

    Mexican Dinosaurs

  • T.R. Holtz

    The phylogenetic position of the Tyrannosauridae: implications for theropod systematics

    Journal of Paleontology

    (1994)
  • T.R. Holtz

    Phylogenetic taxonomy of the Coelurosauria (Dinosauria, Theropoda)

    Journal of Paleontology

    (1996)
  • T.R. Holtz

    A new phylogeny of the carnivorous dinosaurs

    Gaia

    (2000)
  • T.R. Holtz

    The phylogeny and taxonomy of the Tyrannosauridae

  • T.R. Holtz

    Tyrannosauroidea

  • J.R. Horner et al.

    Marine transgressions and the evolution of Cretaceous dinosaurs

    Nature

    (1992)
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