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A Gigantic Shark from the Lower Cretaceous Duck Creek Formation of Texas


Three large lamniform shark vertebrae are described from the Lower Cretaceous of Texas. We interpret these fossils as belonging to a single individual with a calculated total body length of 6.3 m. This large individual compares favorably to another shark specimen from the roughly contemporaneous Kiowa Shale of Kansas. Neither specimen was recovered with associated teeth, making confident identification of the species impossible. However, both formations share a similar shark fauna, with Leptostyrax macrorhiza being the largest of the common lamniform sharks. Regardless of its actual identification, this new specimen provides further evidence that large-bodied lamniform sharks had evolved prior to the Late Cretaceous.


Shark (Chondrichthyes; Elasmobranchii) vertebrae are less common than teeth in the fossil record, and unlike teeth, are relatively undiagnostic at the species level when found in isolation. Nevertheless, isolated vertebrae are scientifically useful as they produce more accurate total body length estimates than do individual teeth [1,2]. Thus, shark vertebrae yield important data on the biology and ecology of fossil sharks, even without clear species association. Here we describe three isolated vertebrae (Sam Noble Oklahoma Museum of Natural History [OMNH] 68860) from a very large lamniform shark found within Albian-age rocks of north-central Texas. Taxonomic identification is difficult, as no teeth were recovered in association with the vertebrae. However, these specimens are important because they represent some of the largest published lamniform shark vertebrae from the Early Cretaceous of North America.

Geologic setting

The specimens described herein, OMNH 68860, were collected in the Duck Creek Formation of Tarrant County, Texas (Fig 1). The Duck Creek is the second lowest formation of the Lower Cretaceous Washita Group (Albian)[3]. Underlying the Duck Creek is the basal Kiamichi Formation, which shares a contact with the Duck Creek defined lithologically by a transition from pebble-conglomerates and breccias to limestone, and faunally by a sharp decrease in Gryphaea and Schloenbachia [4, 5]. The Duck Creek is conformably overlain by the Fort Worth Formation; the intervening contact is lithologically inconspicuous but is instead marked biostratigraphically by the appearance of Holaster simplex, Hemiaster elegans, and Exogyra americana [5].

Fig 1. A map of Albian-age rocks in Tarrant County, Texas, showing the approximate location of OMNH V1727.

Within Tarrant County, the Duck Creek Formation is approximately 13 m thick and is comprised of limestone, marl, and chalky marl deposits exposed in the western half of the county (Fig 1) [4]. The Duck Creek Formation is subdivided into two primary units based on lithology, and four primary zones based on fauna. Lithologically, the first 7 m above the base of the Duck Creek are dominated by limestone. Above 7 m, limestone beds become increasingly indurated, decrease in thickness, and are further interlaminated by marl or marly limestone [4, 6]. Biostratigraphic zones consist of three ammonoid faunas including the basal Desmoceras zone, followed by the Schloenbachia zone and a Scaphites zone; the uppermost faunal zone is marked by the appearance of the brachiopod genus Kingena [4].

The base of a measured section at V1727 begins within the Duck Creek Formation and correlates both lithologically and faunally with the ammonoid-rich limestone beds as described by Winton and Adkins [4] (Fig 2). Limestone dominates the measured section from the base to 6 m, where the first thinly-bedded marl deposits occur. Despite significant portions of the section being covered by talus, the lithological transition to marl-dominated strata above 6 m is clearly defined and further supported by the appearance of Kingena among the talus. The uppermost strata of the measured section consist of weathered, Kingena-bearing marl with various echinoid fragments belonging to Holaster simplex. These taxa imply the transition to the overlying Fort Worth Formation; however, no in situ bedforms were observed; thus, at present, the contact can be inferred but not directly observed.

Initially, the three vertebrae discussed herein were collected from a displaced block of limestone resting among marl debris situated above the lower limestone strata of the Duck Creek Formation. Further specimens bearing similar dimensions, taphonomic characteristics, and proximity to OMNH 68860 were recovered in situ by a private collector within the indurated limestone beds lying just below the Kingena-bearing marls approximately 11.5 m above the base of section (Fig 3; L. Hall, personal communication). The lithology of the strata containing the shark vertebrae found in situ matches the remaining matrix from OMNH 68860. Furthermore, taphonomic similarities shared among all vertebrae indicated that the specimens recovered by the private collector must indeed represent one individual (discussed below). The stratigraphic origin of the shark vertebrae can therefore be confidently placed below the lower Kingena-bearing marl and within the indurated limestone of the upper Duck Creek Formation, approximately 10.5 m above the base of the section.

Fig 3. Additional shark vertebrae found in situ in the same locality as OMNH 68860.

The surrounding lithology correlates with the indurated limestone bedforms 10.5 m above the base of the measured section (photo courtesy of L. Hall, 2013).

Materials and Methods

Size estimation

In order to estimate the total body lengths from individual vertebra, we made comparisons with Cretaceous sharks that possess a more robust postcranial fossil record. As it is impossible to determine vertebral position in a shark based on isolated vertebrae alone [1], we conservatively regard the vertebra with the maximum centrum diameter as the largest vertebra in the entire individual. This ensures that the estimates achieved represent the smallest hypothetical length possible for this specimen. Additionally, we assume that the relationship between vertebral size and total body length is consistent between well-represented species and OMNH 68860. This assumption is reasonable because most pelagic sharks have a consistent body form [2].

Shimada [2] created a formula to estimate total body length from individual vertebrae in Cretoxyrhina mantelli. The relationship between centrum diameter (CD in mm) and total length (TL) can be estimated with the following formula:

Similarly, Gottfried et al. [7] used a different formula to calculate the total body length of individual vertebra in Carcharocles megalodon using Carcharodon carcharias as a proxy.

We calculated total lengths for OMNH 68860 using both formulas.


No permits were required for the described study, which complied with all relevant regulations.

Results and Discussion

Systematic Paleontology

  • Class CHONDRICHTHYES Huxley 1880 [8]
  • Subclass ELASMOBRANCHII Bonaparte 1838 [9]
  • Order LAMNIFORMES Berg 1958 [10]
  • Family, Genus and Species Indet.


OMNH 68860; three vertebral centra, discovered by members of the Paleontology Club of the University of Wisconsin-Milwaukee, and prepared and curated at the Sam Noble Oklahoma Museum of Natural History in Norman, Oklahoma. Specimens were prepared by K. Davies at SNOMNH using a 10% buffered acetic acid bath for two of the three specimens. Additional vertebrae have also been recovered from the same site, but these specimens were not collected by the authors and are currently in a private collection.

Geologic Occurrence.

Indurated limestone interval of the Duck Creek Formation (Lower Cretaceous: Washita Group) of north-central Texas.


The vertebrae were recovered at OMNH locality V1727, northwest of Fort Worth, Tarrant County, Texas (Fig 1). Locality data are on file at OMNH and are available upon request from qualified investigators.


When discovered, all three vertebrae were disarticulated and were separated by a thin layer of limestone. The centra were recovered in a single vertical stack, with one vertebra situated perpendicular to the other two. All three are approximately the same size and proportions, implying that they represent vertebrae from the same area of the body. The largest, most-rostral vertebra measures approximately 110 mm in diameter, with a width of 34 mm (Fig 4). All three are rostrocaudally biconcave (amphicoelous) and roughly spherical in outline, with little to no deformation as a result of crushing. Both of the articular surfaces possess well-marked concentric lamellae on each vertebra. As in other lamniform sharks, all three vertebrae have multiple thin, radial lamellae circumventing at high densities around the outer surface of each centra. These lamellae measure up to 1.3 mm in diameter and run rostrocaudally with occasional bifurcations (Fig 4 right and left lateral view). Both articular surfaces possess a well-developed corpus calcareum, with a thickness measuring approximately 6 mm each.

Fig 4. OMNH 68860 in (descending order) rostral, caudal, ventral, right lateral, dorsal, and left lateral views.

Each vertebra possesses readily distinguishable cartilage foramina on both the dorsal and ventral surfaces. The dorsal surface was identified using techniques described by Shimada et al. [11], where the midline foramina with the smallest inter-pit distance in each centrum are designated the basidorsal cartilage foramina. Surprisingly, each of the two prepared vertebrae has multiple dorsal and ventral foramina (five ventrals, seven dorsals each). The two foramina on the midline are generally the largest; however, most do not extend to contact the corpus calcareum. All foramina are generally square with rounded corners and have a relatively smooth septum traveling into the vertebra. The additional foramina on the dorsal and ventral surface range in size, from 5.2–16.0 mm wide.


There were no other shark fossils associated with OMNH 68860. However, all three possessed traces of encrusting ostreids on the articular surfaces, indicating that these vertebrae were exposed at the surface for some period of time. Further, pyrite has developed near the center of both articular surfaces on the largest vertebra. The smallest of the three vertebrae retains a cast of the next vertebra’s corresponding articular surface, giving this specimen a concavo-convex appearance in lateral view. The three centra also possess a single radial fracture (37 mm long in each vertebra). The common location of this fracture indicates that breakage occurred prior to the rearrangement of the vertebrae. Although it cannot be completely determined whether OMNH 68860 represents reworked material, abrasion is minimal, indicating that transportation was not extensive.


Using the formulas of Shimada [2] and Gottfried et al. [7], and the maximum vertebral diameter of 110 mm, the minimum total length of the individual represented by OMNH 68860 is calculated to be 6.3 and 6.6 m respectively. According to these calculations, OMNH 68860 would rival the largest Cretoxyrhina mantelli specimens (6–7 m) [2] in total length and approximately equal the length of the largest documented extant great white shark (Carcharodon carcharias) (6.4 m) [12].

Although relatively large, OMNH 68860 are not the largest shark vertebrae known from the Early Cretaceous of North America. Shimada [13] described an isolated and incomplete large lamniform shark centrum, Kansas University Vertebrate Paleontology (KUVP) 16343, from the Kiowa Shale of Kansas. This incomplete specimen has a conservative estimated diameter of between 144–170 mm and a calculated complete body length of 8.3–9.8 m. Although smaller, OMNH 68860 compares favorably in appearance to the preserved portions of KUVP 16343 [13]. Shimada [13] tentatively assigned KUVP 16343 to the paraphyletic family Cretoxyrhinidae based on the large size of the specimen and the known presence of other ‘cretoxyrhinid’ sharks from the Kiowa Shale, Cretalamna appendiculata and Leptostyrax macrorhiza (recently reclassified as a member of family Eoptolamnidae [14]); both of which are also found in the Duck Creek Formation of Texas and Oklahoma [15]. Given their large size and the overlapping shark fauna between the two formations in which they were found, we hypothesize that the Kiowa and Duck Creek specimens are from the same species.

Both OMNH 68860 and KUVP 16343 represent relatively large Mesozoic lamniform sharks; however neither specimen would be considered extraordinary compared to some Cenozoic species. For example, an associated specimen of Carcharocles angustidens from the Late Oligocene has an estimated total body length of 6.6 – 9.3 m [16]; roughly matching that OMNH 68860 and KUVP 16343. Neither species, however, comes close to the maximum length estimates for the largest lamniform shark, Carcharocles megalodon. Total length estimates for this species vary depending on the method, but multiple techniques yield a gigantic size ranging from 9.2–16 m [3].


Morphological similarities between the Kiowa and the Duck Creek sharks are further supported by the age of their respective assemblages. Resemblances between the Early Cretaceous marine faunas of Texas and Kansas have long been recognized [17], and more recent studies have indicated that the Kiowa fauna correlates with that of the uppermost Fredericksburg Group and the lower Washita Group of Texas [18]. The index fossil Inoceramus comancheanus is found in the lower Duck Creek Formation and the middle Kiowa Shale, demonstrating that at least some of the Kiowa Shale is equivalent in age to the Duck Creek Formation. Based on their stratigraphy, the Kiowa Shale and Duck Creek have both been placed in the Upper Albian Stage of the Lower Cretaceous [19].

Of the two lamniform species found in both formations, Leptostyrax macrorhiza tend to be larger. In fact, teeth of this species represent some of the largest known shark fossils from the Albian of Texas, making it the most appealing suspect for the identification of OMNH 68860. However, these teeth are still generally smaller than those of the Late Cretaceous Cretoxyrhina mantelli, a species with known vertebral proportions similar to those of OMNH 68860 [15, 20]. However, biostratigraphic evidence suggests that the Texas vertebrae are not from C. mantelli, as teeth from this species do not appear in Texas until the Cenomanian [15]. Further comparisons of OMNH 68860 to those vertebrae of C. mantelli from the Niobrara Formation demonstrate stark differences.

Unlike most sharks, C. mantelli has a surprisingly complete fossil record, with multiple specimens preserving both teeth and postcranial material. Vertebrae from this species tend to be large, exhibiting typical lamnoid-type centra, with a pair of cartilage foramina for both the neural and haemal arches (personal observation). Numerous radiating lamellae are also present that progressively decrease in number caudally down the vertebral column. These vertebrae differ from OMNH 68860 in size, shape, and number of the cartilage foramina. Specifically these foramina in OMNH 68860 do not contact the corpus calcareum, are squarer, and are more numerous than in any published specimens of C. mantelli [11, 20].

Another Late Cretaceous lamniform shark with known postcranial material is Cardabiodon ricki. C. ricki was first described based on teeth and vertebrae from the Cenomanian of Australia [21]. Subsequently, teeth were also described from the Cenomanian of Kansas [22] and the Turonian of central Montana [23]. Superficially, vertebrae from C. ricki are more comparable to the Texas specimens than any of C. mantelli; for example, the vertebrae are more elongate, have a thick corpus calcareum, and small cartilage foramina. However, OMNH 68860 can be differentiated in that they have thinner and less densely spaced radial lamellae, square cartilage foramina, and concentric lamellae. These features, plus the absence of Cardabiodon teeth from the Albian of North America, make it unlikely that the Texas specimen belongs to this genus.

Aside from Leptostyrax macrorhiza, the only other lamniform shark known from both the Kiowa Shale and the Duck Creek Formation is Cretalamna appendiculata. The genus has a relatively long temporal range throughout the Cretaceous, with a worldwide distribution [24, 25]. In Texas, there is an apparent size shift in teeth of C. appendiculata through the Early to Late Cretaceous, where Albian teeth tend to be relatively small, but gradually increase until reaching their largest sizes (up to 30 mm) in the Maastrichtian. These larger Late Cretaceous specimens are considerably abundant in marine fossil sites [15].

Shimada [26] described a relatively complete specimen (Los Angeles County Museum of Natural History [LACM] 128126) of Cretalamna from the Niobrara Formation (Upper Cretaceous). This specimen preserves the 35 anteriormost vertebral centra, with the largest measuring 48 mm in maximum diameter. These vertebrae are of typical lamnoid-form, with lamellae radiating around an amphicoelous centrum. The dorsal foramina are subovate and large, extending to meet the corpus calcareum on both sides. The ventral foramina also abut the corpus calcareum and possess smoothly reinforced edges, giving them a raised appearance [25]. This specimen differs substantially from OMNH 68860. For example, OMNH 68860 contains basidorsal and basiventral foramina that tend to be smaller and do not contact the corpus calcareum. Further, the raised edges of the ventral foramina are absent in this specimen. Lastly, most C. appendiculata tooth fossils from Texas are relatively small (up to 30 mm in height). Using LACM 128126 as an analog (maximum tooth length is 19.9 mm and vertebral width is 48 mm), a Cretalamna with the skeletal proportions of OMNH 68860 should have teeth between 45–50 mm in length. The only known species with teeth of this size from both the Kiowa Shale and the Duck Creek Formation is Leptostyrax macrorhiza (Fig 5).

Fig 5. Reconstruction of the large lamniform sharks from the Duck Creek Formation and Kiowa Shale.

KUVP 16343 and OMNH 68860 are both reconstructed as Leptostyrax macrorhiza and modeled after an odontaspidid. This reconstruction was based on dental similarities shared between Eoptolamnidae and Odontaspididae [14]. Both specimens represent the smallest calculated estimate based on the formula of Shimada [2]. Cretalamna appendiculata is reconstructed as a classic lamnid shark based on shared dental patterns between this genus and members of the family Lamnidae [26].

Alternatively, a third lamniform species is recognized in the Albian of Texas and Kansas. Carcharias amonensis, an odontaspidid, has been reported from the upper Albian Paw Paw Formation and the lower Kiowa Shale [15, 27]. Although this species is not known from associated vertebral material, known teeth are relatively small (11 mm in maximum height [15]), making this species an unlikely candidate for the vertebrae. Given the absolute size and distinct morphology of OMNH 68860, it is highly unlikely that these vertebrae belong to any commonly known shark from the Duck Creek Formation, except possibly Leptostyrax macrorhiza.

Associated skeletal material is unknown for L. macrorhiza, but teeth are relatively abundant. In a recent reevaluation of the genus, Kriwet et al. [14] moved L. macrorhiza into a new family, Eoptolamnidae, along with the genera Protolamna and Eoptolamna. This family is characterized by a weak monognathic heterodonty, a single pair of symphyseal teeth, and high and robust anterior to lateral teeth that possess a well-developed nutritive groove. Interestingly, this group shares many similarities with multiple shark families, including Cretoxyrhinidae, Miitsukurinidae, and Odontaspididae. Unfortunately this diagnosis does not include vertebral characters, but leaves the possibility open that the unique anatomy of the Texas specimen is representative of the group. Further, given the unknown phylogenetic placement of these vertebrae, the size calculations produced here should be viewed as a coarse approximation to the actual size of the animal because lamniform families each possess different skeletal proportions. For example, a modern odontaspidid with a total length of 2.9 m has a largest vertebra equaling 36.6 mm [28]. Using this proportion, OMNH 68860 would have a total length of 8.9 m, or approximately 29% above the smallest calculated total length using Shimada’s [2] equation based on a cretoxyrhinid. Because of the uncertainties regarding the animal’s proportions in life and whether the known material actually represents the largest vertebra in the body, we must assume that the smallest estimates (6.3 m) represent a minimum size for this individual, with the likely possibility that these sharks could far exceed those estimates.

Ecological Implications

Whether or not OMNH 68860 belongs to Leptostyrax remains unclear; however, the unique vertebral morphology and gigantic size indicate the presence of a very large shark during the mid-Cretaceous of North America. The mid-Cretaceous is increasingly being recognized as an important time in shark evolutionary history, as the fossil record improves and increasingly reveals previously unknown diversity. Although Lamniformes likely evolved in the Jurassic, it is not until the Aptian when multiple genera appear together in a single assemblage. Similarly, size increased for the entire order, with multiple families containing relatively large species by the Late Cretaceous [29]. This increase in size and diversity was likely influenced by the warming trend beginning in the mid-Cretaceous; where midocean temperatures at 30–35°N paleolatitude rise from 13–14°C in the early Albian to 28–29°C in the Cenomanian [30]. However, more research is needed to determine the cause of gigantism in lamniform sharks.

This discovery has further implications on the ecology of Mesozoic oceans. In modern oceans, many large lamniform sharks are apex pelagic predators of marine and nearshore ecosystems. Chondrichthyans the size of OMNH 68860 would be among the largest predatory animals of the Albian oceans, dwarfed only by some of the contemporaneous pliosaurs [31, 32]. Fossil tooth marks on dinosaurs [33], mosasaurs [34], plesiosaurs [35], teleost fishes [36], and turtles [37], indicate that large lamniform sharks of the Late Cretaceous occupied the ecological position of generalist predator and scavenger, much as they do today. The discovery of OMNH 68860 highlights an important ecological transition during the Albian, where lamniform sharks begin to take on the massive sizes and trophic abilities seen most predominately in later occurring species. Further, both OMNH 68860 and KUVP 16343 represent Albian species with minimum total lengths between 6.3–8.3 m. This suggests that the late Early Cretaceous was home to some of the largest Mesozoic lamniform sharks of North America.


The principal conclusions of this paper are:

  1. Large shark vertebrae were recovered from the Lower Cretaceous Duck Creek Formation of Texas. These vertebrae represent a single animal of approximately 6.3 m in minimum total length, making this individual one of the largest documented sharks from the Early Cretaceous of N. America.
  2. This specimen has unique morphology undocumented in any other Cretaceous shark from North America, but shares large size with a contemporaneous vertebra from the Kiowa Shale of Kansas.
  3. We hypothesize that these vertebrae belong to Leptostyrax macrorhiza based on their size and co-occurrence in both the Duck Creek Formation and Kiowa Shale. However, without associated teeth, this identification cannot be confirmed.
  4. The Albian oceans contained some of the largest lamniform sharks of the Mesozoic, which hypothetically represented an ecological precursor to the large sharks of the Late Cretaceous and Cenozoic.


We thank the members of the Paleontology Club at the University of Wisconsin-Milwaukee for their involvement in the planning, research, data collection, and recovery of these specimens, allowing us to bring this publication to fruition. We also thank the Paleontology Club academic advisors Dr. M.L Fraiser and Dr. S.Q. Dornbos for their guidance as well as the UWM Department of Geosciences for their support and encouragement. Similarly, all persons involved owe a great debt of gratitude to Mr. L. Hall for his repeated and continuing support and information relay throughout this endeavor and without whose assistance the scientific community may never have known the true stratigraphic origin of these fossils. Further thanks go out to R.A. Farrish for his assistance during the initial reconnaissance and recovery of these specimens. We also express our gratitude to N. Thomas, W.D. Weichert, and D. Wilmeth for their detailed field observations that contributed significantly to the construction of our stratigraphic interpretation. We recognize and thank the contributions of K. Davies, J. Larsen, Dr. R. Cifelli, and the VP volunteers at SNOMNH for preparing, curating, and cataloging these specimens at the SNOMNH. We also thank Dr. L. Wilson for granting access to a comparative collection at the Sternberg Museum of Natural History. We thank Dr. K. Shimada and Dr. M. Becker for sharing their expertise on Mesozoic sharks to the benefit of this project. Last we thank Prof. G. Cuny and Prof. J. Kriwet for their thoughtful and professional reviews of this manuscript.

Author Contributions

Conceived and designed the experiments: JAF SNS JAD-F. Analyzed the data: JAF SNS. Wrote the paper: JAF SNS.


  1. 1. Becker MA, Chamberlain RB, Chamberlain JA (2008) Large carcharhinoid-type shark vertebrae in the Upper Cretaceous of New Jersey: evidence for an anacoracid origin. Northeastern Geology and Environmental Sciences 30: 118–129.
  2. 2. Shimada K (2008) Ontogenetic parameters and life history strategies of the Cretaceous lamniform shark, Cretoxyrhina mantelli, based on the vertebral growth increments. Journal of Vertebrate Paleontology 28: 21–33.
  3. 3. Scott RW, Benson DG, Morin RW, Schaffer BL, Oboh-Ikuenobe FE (2002) Integrated Albian-lower Cenomanian chronostratigraphy standard, Trinity River section, Texas. US Gulf Coast Cretaceous Stratigraphy and Paleoecology Perkins Memorial Volume: 277–344.
  4. 4. Winton WM, Adkins WS (1919) The geology of Tarrant County. University of Texas Bulletin 1931: 1–122.
  5. 5. Bullard FM (1931) The geology of Grayson County, Texas. University of Texas Bulletin 3125: 1–71.
  6. 6. Perkins BF, Albritton CC Jr. (1955) The Washita Group in the valley of the Trinity River, Texas. Fondren Science Series 5: 1–27.
  7. 7. Gottfried MD, Compagno LJV, Bowman SC (1996) Size and skeletal anatomy of the giant megatooth shark Carcharodon megalodon. In: Klimley AP, Ainley DG, editors. Great white sharks: the biology of Carcharodon carcharias. San Diego: Academic Press. pp. 55–89.
  8. 8. Huxley TH (1880) On the application of the laws of evolution to the arrangement of the Vertebrata and more particularly of the Mammalia. Proceedings of the Zoological Society of London 1880: 649–662.
  9. 9. Bonaparte CLJL (1838) Selachorum tabula analytica. Nuovi Annali della Scienze Naturali, Bologna (1)2: 195–214
  10. 10. Berg LS (1958) System der rezenten und fossilen Fischartigen und Fische. Berlin: Deutscher Verlag Wissenschaften. 310 p.
  11. 11. Shimada K, Cumbaa SL, Van Rooyen D (2006) Caudal fin skeleton of the Late Cretaceous shark, Cretoxyrhina mantelli (Lamniformes: Cretoxyrhinidae) from the Niobrara Chalk of Kansas. Bulletin of the New Mexico Museum of Natural History 35: 185–192.
  12. 12. Randall JE (1973) Size of the great white shark (Carcharodon). Science 181: 169–170. pmid:17746627
  13. 13. Shimada K (1997) Gigantic lamnoid shark vertebra from the Lower Cretaceous Kiowa Shale of Kansas. Journal of Paleontology 71: 522–524.
  14. 14. Kriwet J, Klug S, Canudo JI, Cuenca‐Bescos G (2008). A new early Cretaceous lamniform shark (Chondrichthyes, Neoselachii). Zoological Journal of the Linnean Society 154: 278–290.
  15. 15. Welton BJ, Farish RF (1993) The Collector’s Guide to Fossil Sharks and Rays from the Cretaceous of Texas. Lewisville, Texas: Before Time. 204 p.
  16. 16. Gottfried MD, Fordyce RE (2001) An associated specimen of Carcharodon angustidens (Chondrichthyes, Lamnidae) from the Late Oligocene of New Zealand, with comments on Carcharodon interrelationships. Journal of Vertebrate Paleontology 21: 730–739.
  17. 17. St. John OP (1887) Notes on the geology of southwest Kansas: Kansas State Board of Agriculture, 5th Biennial Report: 132–152.
  18. 18. Cobban WA, Reeside JB Jr. (1952) Correlation of the Cretaceous formations of the Western Interior of the United States: Geological Society of America, Bulletin, 63: 1011–1044.
  19. 19. Scott RW (1970) Paleoecology and paleontology of the Lower Cretaceous Kiowa Formation, Kansas. The University of Kansas Paleontological Contributions 52: 5–94.
  20. 20. Shimada K (1997) Skeletal anatomy of the Late Cretaceous lamniform shark, Cretoxyrhina mantelli from the Niobrara Chalk in Kansas. Journal of Vertebrate Paleontology 17: 642–652.
  21. 21. Siverson M (1999). A new large lamniform shark from the uppermost Gearle Siltstone (Cenomanian, Late Cretaceous) of Western Australia. Transactions of the Royal Society of Edinburgh: Earth Sciences 90: 49–66.
  22. 22. Dickerson AA, Shimada K, Reilly B, Rigsby CK (2013). New data on the Late Cretaceous cardabiodontid lamniform shark based on an associated specimen from Kansas. Transactions of the Kansas Academy of Science 115: 125–133.
  23. 23. Siverson M, Lindgren J (2005). Late Cretaceous sharks Cretoxyrhina and Cardabiodon from Montana, USA. Acta Palaeontologica Polonica 50: 301–314.
  24. 24. Cappetta H (1987) Handbook of palaeoichthyology. Volume 3B. Mesozoic and Cenozoic Elasmobranchii: Chondrichthyes. Stuttgart; New York: Gustav Fisher Verlag. 193 p.
  25. 25. Siverson M, Lindgren J, Newbrey MG, Cederström P, Cook TD (2013). Late Cretaceous (Cenomanian–Campanian) mid-palaeolatitude sharks of Cretalamna appendiculata type. Acta Palaeontologica Polonica: in press.
  26. 26. Shimada K (2007) Skeletal and dental anatomy of lamniform shark, Cretalamna appendiculata, from Upper Cretaceous Niobrara Chalk of Kansas. Journal of Vertebrate Paleontology 27: 584–602.
  27. 27. Everhart MJ (2009) First occurrence of marine vertebrates in the Early Cretaceous of Kansas: Champion Shell Bed, basal Kiowa Formation. Transactions of the Kansas Academy of Science 112: 201–210.
  28. 28. Hansen BB, Cuny G, Rasmussen BW, Shimada K, Jacobs P, Heilmann-Clausen C (2013) Associated skeletal and dental remains of a fossil odontaspidid shark (Elasmobranchii: Lamniformes) from the Middle Eocene Lillebælt Clay Formation in Denmark. Bulletin of the Geological Society of Denmark 61: 37–46.
  29. 29. Underwood CJ (2006) Diversification of the Neoselachii (Chondrichthyes) during the Jurassic and Cretaceous. Paleobiology 32: 215–235.
  30. 30. Pucéat E, Lécuyer C, Sheppard SM, Dromart G, Reboulet S, Grandjean P (2003) Thermal evolution of Cretaceous Tethyan marine waters inferred from oxygen isotope composition of fish tooth enamels. Paleoceanography 18: 1–12.
  31. 31. Longman HA (1924) Kronosaurus queenslandicus. A gigantic Cretaceous pliosaur. Memoirs of the Queensland Museum 10: 1–7.
  32. 32. Kear BP (2003) Cretaceous marine reptiles of Australia: a review of taxonomy and distribution. Cretaceous Research 24: 277–303.
  33. 33. Everhart MJ, Hamm SA (2005) A new nodosaur specimen (Dinosauria: Nodosauridae) from the Smoky Hill Chalk (Upper Cretaceous) of western Kansas. Transactions of the Kansas Academy of Science 108: 15–21.
  34. 34. Everhart MJ (2004) Late Cretaceous interaction between predators and prey. Evidence of feeding by two species of shark on a mosasaur. PalArch, Vertebrate Palaeontology Series 1: 1–7.
  35. 35. Everhart MJ (2005) Bite marks on an elasmosaur (Sauropterygia: Plesiosauria) paddle from the Niobrara Chalk (Upper Cretaceous) as probable evidence of feeding by the lamniform shark, Cretoxyrhina mantelli. PalArch, Vertebrate Paleontology Series 2: 14–24.
  36. 36. Shimada K, Everhart MJ (2004) Shark-bitten Xiphactinus audax (Teleostei: Ichthyodectiformes) from the Niobrara Chalk (Upper Cretaceous) of Kansas. Mosasaur 7: 35–39.
  37. 37. Shimada K, Hooks GE III (2004) Shark-bitten protostegid turtles from the Upper Cretaceous Mooreville Formation of Alabama. Journal of Paleontology 78: 205–210.