Carcharodontosaurus

Carcharodontosaurus
Temporal range: EarlyLate Cretaceous, 100–93 Ma
Cast of a Carcharodontosaurus skull in Santa Barbara
Scientific classification
Kingdom: Animalia
Phylum: Chordata
Class: Reptilia
Superorder: Dinosauria
Order: Saurischia
Suborder: Theropoda
Family: Carcharodontosauridae
Subfamily: Carcharodontosaurinae
Stromer, 1931
Genus: Carcharodontosaurus
Stromer, 1931
Species
  • C. saharicus (Depéret & Savornin, 1927) (type)
  • C. iguidensis Brusatte & Sereno, 2007

Carcharodontosaurus (play /ˌkɑrkərɵˌdɒntɵˈsɔrəs/) was a gigantic carnivorous carcharodontosaurid dinosaur that lived around 100 to 93 million years ago, during the late Albian to early Cenomanian stages of the mid-Cretaceous Period. It was discovered to be the second largest predatory dinosaur, larger than Tyrannosaurus and Giganotosaurus, but not as large as Spinosaurus.

The Carcharodontosaurus is named after the shark genus Carcharodon (from the Greek καρχαρο karcharo meaning "jagged" or "sharp" and οδοντο odonto meaning "teeth", and σαυρος sauros, meaning "lizard"[1]) — "jagged-toothed lizard" or "sharp-toothed lizard".

Contents

Description

Life restoration of Carcharodontosaurus saharicus

Carcharodontosaurus is one of the longest and heaviest known carnivorous dinosaurs, with various scientists proposing length estimates ranging between 12 and 13 m (39-43.5 ft) and weight estimates between 6 and 15 metric tons.[2]

Carcharodontosaurus was a carnivore, with enormous jaws and long, serrated teeth up to eight inches long. Paleontologists once thought that Carcharodontosaurus had the longest skull of any of the theropod dinosaurs. However, the premaxilla and quadrate bones were missing from the original African skull, which led to misinterpretation of its actual size by researchers. A more modest length of 1.6 meters (5.2 ft) has now been proposed for C. saharicus, and the skull of C. iguidensis is reported to have been slightly larger at 1.75 m in length (5.5 ft).[3] Currently, the largest known theropod skull belongs to another huge carcharodontosaurid dinosaur, the closely related Giganotosaurus (with skull length estimates up to 1.95 m) (6.3 ft).[4]

Brain and inner ear

In 2001, Hans C. E. Larsson published a description of the inner ear and endocranium of Carcharodontosaurus saharicus.[5] Larsson observed that the C. saharicus braincase "completely encloses the endocranial region." This "high degree of ossification" made his analysis of its anatomy significantly easier to perform.[6] The C. saharicus endocast is similar to that of a related dinosaur, Allosaurus fragilis.[6] Larsson describes the olfactory bulbs and peduncles as lying "on approximately the same horizontal plane as the forebrain."[7] The midbrain is angled downwards and towards the rear of the animal, while the hind brain is roughly parallel to the forebrain.[7] The cephalic flexure, the bend between the fore- and midbrain, has an angle of 45 degrees.[8] The pontine flexure, the bend between the mid- and hindbrain has an angle of about 40 degrees.[8] Carcharodontosaurus had a large optic (II) nerve.[9] The C. saharicus vena capitis dorsalis "drains the anterior neck muscles through a pair of long canals on the posterior surface of the endocast."[10] This configuration is found in Allosaurus and Dromaeosaurus albertensis, although in C. saharicus and Troodon "the transverse sinus probably drained into a middle cerebral vein that exited the brain in the ridge present on the dorsal edge of the trigeminal foramen."[10]

Size comparison of selected giant theropod dinosaurs, C. saharicus in violet
Allosaurus fragilis skull. Allosaurus and Carcharodontosaurus had very similar reptile-like brain and inner ear anatomy.

The three semicircular canals of the inner ear of Carcharodontosaurus saharicus, when viewed from the side, had a subtriangular outline.[10] This subtriangular inner ear configuration is present in Allosaurus, lizards, turtles, but not in birds.[10] The pointed apex "at the junction of the anterior and posterior semicircular canals" is caused by the near linearity of the canals and closely resembles the condition of modern crocodiles.[10] The subtriangular configuration may be the basal condition of archosauromorphs.[10] A recess which would have held the floccular lobe of the brain projects into the area surrounded by the semicircular canals.[11] This condition is also present in other non-avian theropods, birds, and pterosaurs.[12] The orientation of the lagena of C. saharicus resembles the condition in crocodilians and some birds.[12] The extent of its perilymphatic duct resembled those of Varanus, crocodilians, and birds.[12] The crista which would have supported the secondary tympanic membrane in C. saharicus was either absent, or not preserved.[13] This contrasts with Troodon, whose crista were ossified at least in their dorsal and ventral regions and their remaining portions either cartilaginous or too delicate to be preserved.[13] The metotic strut of C. saharicus is reduced and medial compared to the "laterally hypertrophied" condition of non-avian maniraptors like Dromaeosaurus and Troodon, as well as primitive birds like Archaeopteryx and Hesperornis.[13]

Traditional comparisons of brain volume to body mass has estimated brain size as the volume of the endocast.[14] However, the brain of Sphenodon fills only about half of its endocranial volume.[15] Some paleontologists used the fifty percent estimate to ascertain the brain size of dinosaur endocasts.[14] Other workers have observed that details on the endocranial surface indicates that some fossil reptiles had brains that occupied a much larger portion of the endocranium.[16] Larsson notes that the transition from reptiles to birds prevents using a set ratio from being a valid approach to estimating the volume of the endocranium occupied by a dinosaur's brain.[16]

Adding difficulty to examining the ratio of the brain volume of a dinosaur to its body mass is the wide range of estimates for live mass.[16] Larsson observes that one study which estimated the live masses for many dinosaur genera typically had a fourfold range.[16]

Dromaeosaurus albertensis skull. Dromaeosaurus and Carcharodontosaurus had somewhat similar vasculature near the brain, but slightly differing inner ear anatomy.

Larsson laments that "[t]he broad ranges of body mass estimates, combined with the ambiguous ratio of endocranial volume occupied by the brain, present a high degree of uncertainty for [creating an] index of brain size."[16] Consequently, he attempted to minimize errors in his study by making a different kind of comparison.[16]

Life restoration of C. saharicus.

Noting that while it is difficult to estimate the absolute volume of the brain, the proportions of its various regions should the same in the endocast as it was in the large brain Larsson's study compared the ratio of the cerebrum, which is highly demarcated, to the rest of the endocast's volume.[16] However, if the thickness of the dura covering the various parts of the brain itself differed, then that could alter the relative proportions within the endocast.[16] In Caiman the dura covering the medullary region seemed to increase proportionally in thickness compared to the dura covering the forebrain, although this might not impact the ratio between the regions.[16] Nevertheless, Larsson reaffirmed the superiority of his technique to traditional comparisons of brain volume to estimated live body mass.[16]

"As brain mass increases, cerebral mass increases with slight negative allometry in nonavian reptiles," Larsson concludes, larger nonavian reptile have proportionately smaller cerebra than smaller ones.[17] Further, the opposite is true in birds, larger avian brains have cerebra which are slightly larger, proportionally speaking.[17] Larsson found that both C. saharicus and Allosaurus lie within the 95% confidence limits of the nonavian reptile ratio, while Tyrannosaurus lies just outside it in the direction of a more avian proportion.[18] The extinct crocodile Sebecus had a ratio similar to those of the non-coelurosaurian theropods studied.[18] Since tyrannosaurs are coelurosaurs, this is evidence that the advent of the Coelurosauria marks the beginning of trend in theropod brain enlargement.[18]

Pathology

SGM-Din 1, a Carcharodontosaurus saharicus skull, has a circular puncture wound in the nasal and "an abnormal projection of bone on the antorbital rim".[19]

Discovery, etymology and taxonomic history

Carcharodontosaurus tooth, which was found in the Sahara Desert, compared to a Carcharodon megalodon tooth and an American quarter.

Carcharodontosaurus fossils were first found by Charles Depéret and J. Savornin in the Continental intercalaire of Algeria (dating to the Albian stage) in 1927. Originally called Megalosaurus saharicus[20] (many theropods were once erroneously referred to as Megalosaurus), its name was changed in 1931 by Ernst Stromer von Reichenbach to that used today. Stromer named Carcharodontosaurus "for its mainly Carcharodon-like teeth", which were "not recurved, almost bilaterally symmetrical but with convex edges."[1] Further fossils were collected from the Baharija Formation of Egypt, dating to the slightly later Cenomanian stage. These first fossils of Carcharodontosaurus were destroyed during World War II. However, cranial material from a Carcharodontosaurus was again discovered in the Kem Kem Formation of Morocco in 1995 by paleontologist Paul Sereno. Stephen Brusatte and Paul Sereno reported a second species of Carcharodontosaurus, found in the Echkar Formation of Niger, differing from C. saharicus in some aspects of the maxilla and braincase.[21] This second species, which was discovered in Niger in 1997, was named C. iguidensis in December 2007.[22]

Footnotes

  1. ^ a b Stromer (1931).
  2. ^ Sereno, et al. (1996). Seebacher (2001). Therrien and Henderson (2007).
  3. ^ Briggs (2007).
  4. ^ Calvo and Coria (1998).
  5. ^ "Abstract," Larsson (2001). Page 19.
  6. ^ a b "Description," Larsson (2001). Page 20.
  7. ^ a b "Description," Larsson (2001). Pages 20-21.
  8. ^ a b "Description," Larsson (2001). Page 21.
  9. ^ "Description," Larsson (2001). Page 22.
  10. ^ a b c d e f "Description," Larsson (2001). Page 23.
  11. ^ "Description," Larsson (2001). Pages 23-24.
  12. ^ a b c "Description," Larsson (2001). Page 24.
  13. ^ a b c "Description," Larsson (2001). Page 25.
  14. ^ a b "Allometric Comparison," Larsson (2001). Page 25.
  15. ^ "Allometric Comparison," Larsson (2001). Pages 25-26.
  16. ^ a b c d e f g h i j "Allometric Comparison," Larsson (2001). Page 26.
  17. ^ a b "Allometric Comparison," Larsson (2001). Page 27.
  18. ^ a b c "Allometric Comparison," Larsson (2001). Page 29.
  19. ^ "Acrocanthosauridae fam. nov.," in Molnar (2001). Pg. 342.
  20. ^ Deparet and Savornin (1927).
  21. ^ Brusatte and Sereno (2005).
  22. ^ Brusatte and Sereno (2007).

References

  • Briggs, Helen (2007-12-12). "New meat-eating dinosaur unveiled" (Web). News article about; Carcharodontosaurus iguidensis was one of the largest meat-eaters that ever lived. BBC NEWS. http://news.bbc.co.uk/2/hi/science/nature/7138782.stm. Retrieved December 15, 2007. 
  • Brusatte, S. and Sereno, P.C. (2005). "A new species of Carcharodontosaurus (Dinosauria: Theropoda) from the Cenomanian of Niger and its implications for allosauroid phylogeny." Journal of Vertebrate Paleontology, 25: 40A.
  • Brusatte, S.L. and Sereno, P.C. (2007). "A new species of Carcharodontosaurus (dinosauria: theropoda) from the Cenomanian of Niger and a revision of the genus." Journal of Vertebrate Paleontology, 27(4): .
  • Calvo, J.O., and Coria, R.A. (1998) "New specimen of Giganotosaurus carolinii (CORIA & SALGADO, 1995), supports it as the largest theropod ever found." Gaia, 15: 117–122.
  • Deparet, C. and Savornin, J. (1927). "Sur la decouverte d'une faune de vertebres albiens a Timimoun (Sahara occidental)." Comptes Rendus, Academie du Sciences, Paris, 181: 1108-1111.
  • Discovery Channel Videos: Monsters Resurrected: Biggest Killer Dino
  • Larsson, H.C.E. 2001. Endocranial anatomy of Carcharodontosaurus saharicus (Theropoda: Allosauroidea) and its implications for theropod brain evolution. pp. 19–33. In: Mesozioc Vertebrate Life. Ed.s Tanke, D. H., Carpenter, K., Skrepnick, M. W. Indiana University Press.
  • Seebacher, F. (2001). "A new method to calculate allometric length-mass relationships of dinosaurs." Journal of Vertebrate Paleontology, 21(1): 51–60.
  • Sereno, P. C., D. B. Dutheil, M. Iarochene, H. C. E. Larsson, G. H. Lyon, P. M. Magwene, C. A. Sidor, D. J. Varricchio, and J. A. Wilson. (1996). "Predatory dinosaurs from the Sahara and the Late Cretaceous faunal differentiation." Science, 272: 986–991.
  • Stromer, E. (1931). "Wirbeltiere-Reste der Baharijestufe (unterestes Canoman). Ein Skelett-Rest von Carcharodontosaurus nov. gen." Abhandlungen der Bayerischen Akademie der Wissenschaften, Mathematisch-naturwissenschaftliche Abteilung, 9(Neue Folge): 1–23.
  • Therrien, F.; and Henderson, D.M. (2007). "My theropod is bigger than yours...or not: estimating body size from skull length in theropods". Journal of Vertebrate Paleontology 27 (1): 108–115. doi:10.1671/0272-4634(2007)27[108:MTIBTY]2.0.CO;2. 

External links

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