Deinonychosauria

Bilateria

Deinonychosaurs
Temporal range: Middle Jurassic-Late Cretaceous, 167–65.5 Ma
Mounted skeleton of Deinonychus antirrhopus
Scientific classification
Phylum: Chordata
Class: Reptilia
Superorder: Dinosauria
Order: Saurischia
Suborder: Theropoda
Apomorphy: Aviremigia
Branch: Paraves
Infraorder: Deinonychosauria
Colbert & Russell, 1969
Subgroups

The Deinonychosauria ("fearsome claw lizards") were a clade of coelurosaurian theropod dinosaurs from the Late Jurassic and Cretaceous periods. These omnivores and carnivores are known for their switchblade-like second toe claws and for displaying numerous bird-like characteristics. The clade has been divided into two further groups — Dromaeosauridae and Troodontidae. The largest known of these was Utahraptor (7 m or 23 ft), and Anchiornis was the smallest (34 cm or 13 in). By modern classifications, birds are closely related to this group of dinosaurs, and share a common ancestor with them.

Contents

Description

Like other theropods, deinonychosaurs were bipedal; that is, they walked on their two hind legs. However, whereas most theropods walked with three toes contacting the ground, fossilized footprint tracks confirm that most deinonychosaurs held the second toe off the ground in a hyperextended position, with only the third and fourth toes bearing the weight of the animal. This is called functional didactyly.[1] The enlarged second toe bore an unusually large, curved sickle-shaped claw (held off the ground or 'retracted' when walking). This claw was especially large and flattened from side to side in the large-bodied predatory eudromaeosaurs.[2] The first toe (hallux) was relatively small and angled inward toward the center of the body, but was not fully reversed as in modern birds.[3] One eudromaeosaur species, Balaur bondoc, possessed a first toe which was highly modified in parallel with the second. Both the first and second toes on each foot of B. bondoc were held retracted and bore enlarged, sickle-shaped claws.[4]

The teeth of deinonychosaurs were curved and serrated, but not blade-like except in some advanced species such as Dromaeosaurus albertensis. The serrations on the front edge of deinonbychosaur teeth were very small and fine, while the back edge had serrations which were very large and hooked.[3] Deinonychosaurs generally had long, winged forelimbs, though these were smaller in some troodontids. The wings usually bore three large, flexible claws.[3]

Most deinonychosaurs seem to have been predatory, though some smaller species especially among the troodontids are known to have been at least omnivorous.[5][3]

Claw function

One of the best-known features of deinonychosaurs is the presence of an enlarged and strongly curved "sickle claw" on a hyper-extendible second toe, modified to hold the sickle claw clear of the ground when walking. While this characteristic claw and its associated modifications to the anatomy of the foot (such as a shortened metatarsus in eudromaeosaurs) had been known since the mid 20th Century, their possible functions were the subject mainly of speculation, and few actual studies were published. Initial speculation regarded the claws as slashing implements used to disembowel large prey. In this scenario, the shortened upper foot would serve as an anchor point for powerful tendons to improve kicking ability. However, subsequent studies of the actual claw shape showed that the underside of the claw was only weakly keeled and would not have been an effective cutting instrument. Instead, it appeared to be more of a hooking implement. Manning et al. suggested in 2006 that the claws were similar to crampons and were used for climbing, and in the case of larger species or individuals, climbing up the flanks of very large prey.[6]

A larger study of deinonychosaur claw function, published in 2011 by Fowler and colleagues, concluded that the earlier study by Manning and colleagues was correct and that the "sickle claws" of deinonychusaurs would have been ineffective as cutting weapons. They compared the claw and overall foot anatomy of various deinonychosaurs with modern birds to shed light on their actual function. Fowler and colleagues showed that many modern predatory birds also have enlarged claws on the second toes. In modern raptors, these claws are used to help grip and hold prey of sizes smaller than or equal to the predator, while the birds use their body weight to pin their prey to the ground and eat it alive.[3] Folwer and colleagues suggested that this behavior is entirely consistent with the anatomy of advanced deinonychosaurs like Deinonychus, which had slightly opposing first toes and strong tendons in the toes and foot. This makes it likely that advanced dromaeosaurids also used their claws to puncture and grip their prey to aid in pinning it to the ground, while using shallow wing beats and tail movements to stabilize themselves.[3] Other lines of evidence for this behavior include teeth which had large, hooked serrations only on the back edge (useful in pulling flesh upward rather than slicing it) and large claws on the wings (for greater maneuvering of prey while mantling it with the wings).[3]

In more primitive dromaeosaurids and in troodontids, the feet were not as specialized and the claws were not as large or as hooked. Additionally, the toe joints allowed more range of motion than the simple up-down movements of advanced dromaeosaurids. This makes it likely that these species specialized in smaller prey that could be pinned using only the inner toes, not requiring the feet to be as strong or sturdy.[3]

Classification

Dromaeosauridae

The subgroup dromaeosauridae includes such dinosaurs as Velociraptor and Deinonychus. They are commonly called "raptors" and were smart, fast, and agile hunters that may have cooperated in groups.

Troodontidae

Much less is known about the dromaeosaurids' sister group, the troodontids, because fossils of them are less common. The best known troodontids are Troodon and Saurornithoides. Troodontids were generally small and slender, and had long, narrow skulls containing sharp, curved teeth.[7] They may be the most intelligent dinosaurs known, with a remarkably large brain-to-body mass ratio. Like their sister group, they were smart, active and agile hunters who displayed bird-like characteristics.

Taxonomy

References

  1. ^ Li, Rihui; Lockley, M.G., Makovicky, P.J., Matsukawa, M., Norell, M.A., Harris, J.D. and Liu, M. (2007). "Behavioral and faunal implications of Early Cretaceous deinonychosaur trackways from China". Naturwissenschaften 95 (3): 185–91. doi:10.1007/s00114-007-0310-7. PMID 17952398. http://www.springerlink.com/content/v1u455854212404r/. 
  2. ^ Longrich, N.R.; Currie, P.J. (2009). "A microraptorine (Dinosauria–Dromaeosauridae) from the Late Cretaceous of North America". PNAS 106 (13): 5002–7. doi:10.1073/pnas.0811664106. PMC 2664043. PMID 19289829. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=2664043. 
  3. ^ a b c d e f g h Fowler, D.W., Freedman, E.A., Scannella, J.B., and Kambic, R.E. (2011). "The Predatory Ecology of Deinonychus and the Origin of Flapping in Birds." PLoS ONE, 6(12): e28964. doi:10.1371/journal.pone.0028964
  4. ^ Z., Csiki; Vremir, M.; Brusatte, S. L.; and Norell, M. A. (in press). "An aberrant island-dwelling theropod dinosaur from the Late Cretaceous of Romania". Proceedings of the National Academy of Sciences of the United States of America 107 (35): 15357–61. doi:10.1073/pnas.1006970107. PMC 2932599. PMID 20805514. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=2932599.  Supporting Information
  5. ^ Zanno, L.E. and Makovicky, P.J. (2011). "Herbivorous ecomorphology and specialization patterns in theropod dinosaur evolution." Proc Natl Acad Sci USA, 108: 232–237.
  6. ^ Manning, P.L., Payne, D., Pennicott, J., Barrett, P.M., and Ennos, R.A. (2006). "Dinosaur killer claws or climbing crampons?" Biology Letters, 22: 110–112.
  7. ^ Troodontids - Berkeley.edu
  8. ^ Xing Xu, Hailu You, Kai Du and Fenglu Han (28 July 2011). "An Archaeopteryx-like theropod from China and the origin of Avialae". Nature 475 (7357): 465–470. doi:10.1038/nature10288. PMID 21796204. http://www.nature.com/nature/journal/v475/n7357/full/nature10288.html.