Temporal range: Upper Jurassic–Upper Cretaceous
|SPV 300/45 foot model.|
Dromaeosaurs had a world-wide distribution. They first appeared in the Middle Jurassic, 167 million years ago (mya). The larger types are not found before about 124 mya in the Lower Cretaceous, and are only found in the northern hemisphere. They survived until the end of the Cretaceous, 65.5 mya at the K/T extinction event.
The presence of dromaeosaurs in the Middle Jurassic is shown by isolated fossil teeth, though no dromaeosaurid body fossils have been found this early.
Description[change | change source]
The Dromaeosaur skeleton suggests they were active, fast-running, and closely related to birds.
Dromaeosaurs, like most other theropods, had an S-curved neck, and their trunk was relatively short and deep. Like other maniraptorans, they had long arms, and relatively large hands with three long fingers ending in large claws.
The dromaeosaur hip structure featured a large 'pubic boot' (part of the hip) projecting beneath the base of the tail. These hip bones were places muscle and tendons attached.
Dromaeosaur feet bore a large, recurved claw on the second toe. Their tails were slender, and mainly used as a counter-balance.
Some, and probably all, dromaeosaurs were covered in feathers, including large, vaned, wing and tail feathers.
Foot[change | change source]
Like other theropods, dromaeosaurs were bipedal; that is, they walked on their hind legs. Whereas other theropods walked with three toes on the ground, fossilized footprint tracks show that most dromaeosaurs held the second toe off the ground, with only the third and fourth toes bearing the weight of the animal. The enlarged second toe bore an unusually large, curved sickle-shaped claw. It is thought to have been used in capturing prey and, in the smaller species, climbing trees.
One dromaeosaur species, Balaur bondoc, had 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 also held retracted and bore enlarged, sickle-shaped claws.
Tail[change | change source]
Dromaeosaurs had long tails. Most of the tail vertebrae bear bony, rod-like extensions, as well as bony tendons in some species. In his study of Deinonychus, Ostrom proposed that these features stiffened the tail so that it could only flex at the base, and the whole tail would then move as a single, rigid, lever. However, one well-preserved specimen of Velociraptor mongoliensis (IGM 100/986) has an articulated tail skeleton which is curved horizontally in an S-shape. This suggests that, in life, the tail could bend from side to side with some degree of flexibility. It has been proposed that this tail was used as a stabilizer and/or counterweight while running. In Microraptor, an elongate diamond-shaped fan of feathers is preserved on the end of the tail. This might have been used as a stabilizer and rudder during gliding.
Size[change | change source]
Dromaeosaurs were small to medium-sized dinosaurs, ranging from about 0.7 meters in length (2.3 ft, in the case of Mahakala) to over 6m (20 ft, in Utahraptor and Achillobator). Some were larger; undescribed specimens of Utahraptor in BYU collections may have been up to 11 m (36 ft) long. Large size appears to have evolved at least twice among dromaeosaurs. A possible third lineage of giant dromaeosaurs is represented by isolated teeth found on the Isle of Wight, England. The teeth belong to a Utahraptor-sized animal but are more similar in shape to the teeth of velociraptorines.
Mahakala is both the most primitive dromaeosaur ever described and the smallest. This evidence, and Microraptor and the troodontid Anchiornis, suggests the common ancestor of dromaeosaurs, troodontids, and birds – the 'ancestral paravian' – may have been very small, at around 65 cm in length and 600 to 700 grams of mass.
Feathers[change | change source]
Fossils show that dromaeosaurs were covered in feathers. Some fossils preserve long feathers on the hands and arms (remiges) and tail (rectrices), as well as shorter, down-like feathers covering the body.
Other fossils, which do not preserve actual impressions of feathers, still preserve the associated bumps on the forearm bones where long wing feathers would have attached in life. Overall, this feather pattern looks very much like Archaeopteryx.
Many other dromaeosaur fossils have been found with feathers covering their bodies, some with fully-developed feathered wings. Microraptor even shows evidence of a second pair of wings on the hind legs. While direct feather impressions are only possible in fine-grained sediments, some fossils found in coarser rocks show evidence of feathers by the presence of quill knobs, the attachment points for wing feathers possessed by some birds. The dromaeosaurids Rahonavis and Velociraptor have both been found with quill knobs, showing that these forms had feathers despite no impressions having been found.
In light of this, it is most likely that even the larger ground-dwelling dromaeosaurs bore feathers, since even flightless birds today retain most of their plumage, and relatively large dromaeosaurs, like Velociraptor, are known to have had feathers.
Paleobiology[change | change source]
Claw function[change | change source]
There is some discussion about the function of the enlarged "sickle claw" on the second toe. When John Ostrom described it for Deinonychus in 1969, he interpreted the claw as a blade-like slashing weapon, much like the canines of some saber-toothed cats, used with powerful kicks to cut into prey. Adams (1987) suggested that the talon was used to disembowel large ceratopsian dinosaurs. The interpretation of the sickle claw as a killing weapon applied to all dromaeosaurs.
In Manning's interpretation, the second toe claw would be used as a climbing aid when subduing bigger prey and also as stabbing weapon.
Ostrom compared Deinonychus to the ostrich and cassowary. He noted that the bird species can inflict serious injury with the large claw on the second toe. The cassowary has claws up to 125 millimetres (4.9 in) long. The seriema also has an enlarged second toe claw, and uses it to tear apart small prey items for swallowing.
The Manning team also compared the curvature of the dromaeosarid "sickle claw" on the foot with curvature in modern birds and mammals. Previous studies had shown that the amount of curvature in a claw corresponded to what lifestyle the animal has: animals with strongly curved claws of a certain shape tend to be climbers, while straighter claws indicate ground-dwelling lifestyles. The sickle-claws of the dromaeosaurid Deinonychus have a curvature of 160 degrees, well within the range of climbing animals. The forelimb claws they studied also fell within the climbing range of curvature.
Paleontologist Peter Mackovicky said that small, primitive dromaeosaurids (such as Microraptor) were likely to have been tree-climbers, but that climbing did not explain why later, gigantic dromaeosaurids such as Achillobator retained highly curved claws when they were too large to have climbed trees.
Group behavior[change | change source]
Deinonychus fossils have been uncovered in small groups near the remains of the herbivore Tenontosaurus, a larger ornithischian dinosaur. This had been interpreted as evidence that these dromaeosaurs hunted in coordinated packs like some modern mammals. However, not all paleontologists found the evidence conclusive, and a study in 2007 by Roach and Brinkman suggests that the Deinonychus may have actually displayed a disorganized mobbing behavior.
The first known extensive dromaeosaur trackway was found in Shandong, China.
The trackway, (made by a large, Achillobator-sized species), showed the sickle-claw was held off the ground. Six individuals of about equal size moved together along a shoreline. The individuals were spaced about one meter apart, and retained the same direction of travel, walking at a fairly slow pace. The trackways are evidence that some species of dromaeosaurs lived in groups. While the trackways clearly do not represent hunting behavior, the idea that groups of dromaeosaurs may have hunted together can not be ruled out.
Flying and gliding[change | change source]
The ability to fly or glide has been suggested for at least two dromaeosaur genera. The first, Rahonavis was originally classified as avian bird, but found to be a dromaeosaur in later studies. It may have been capable of powered flight. The forelimbs of Rahonavis were more powerfully built than Archaeopteryx, and show evidence that they bore strong ligament attachments necessary for flapping flight. Luis Chiappe concluded that, given these adaptations, Rahonavis could probably fly but would have been more clumsy in the air than modern birds.
Another species of dromaeosaur, Microraptor, may have been capable of gliding using its well-developed wings on both the fore and hind limbs. A 2005 study by Sankar Chatterjee suggested that the wings of Microraptor functioned like a split-level "biplane", and that it likely employed a style of gliding, in which it would launch from a perch and swoop downward in a 'U' shaped curve, then lift again to land on another tree, with the tail and hind wings helping to control its position and speed. Chatterjee also found that Microraptor had the basic requirements to sustain level powered flight in addition to gliding.
Classification[change | change source]
Relationship with birds[change | change source]
- Further information: Origin of birds
Mark Norell and colleagues analyzed a survey of coelurosaur fossils and suggested that dromaeosaurs were most closely related to birds, with troodontids as a more distant outgroup. In 2002, Hwang and colleagues suggested that birds (avialans) were better thought of as cousins to the dromaeosaurids and troodontids.
The current consensus among paleontologists agrees with Hwang that dromaeosaurids are most closely related to the troodontids, and together with the troodontids form the clade Deinonychosauria. Deinonychosaurians in turn are the sister taxon to avialans, and therefore the closest relatives of avialan birds.
A consensus of paleontologists has concluded that there is not yet enough evidence to say whether any dromaeosaurs could fly or glide, or whether they evolved from ancestors that could.
Other ideas[change | change source]
In 2002, Hwang et al. found that Microraptor was the most primitive dromaeosaur. Xu and colleagues in 2003 cited the basal position of Microraptor, along with feather and wing features, as evidence that the ancestral dromaeosaur could glide. In that case the larger dromaeosaurs would be secondarily terrestrial—having lost the ability to glide later in their evolutionary history.
A few researchers, like Larry Martin, believe that dromaeosaurs, along with all maniraptorans are not dinosaurs at all. Martin asserted for decades that birds were unrelated to maniraptorans, but in 2004 he changed his position, and now he agrees that the two are the closest of relatives. Martin believes that maniraptorans are secondarily flightless birds, and that birds evolved from non–dinosaurian archosaurs, so that most of the species formerly called theropods would now not even be classified as dinosaurs.
A challenge to all of these alternative scenarios came when Turner and colleagues in 2007 described a new dromaeosaur, Mahakala, which they found to be the most basal and most primitive member of the Dromaeosauridae, more primitive than Microraptor.
Mahakala had short arms and no ability to glide. Turner et al. also inferred that flight evolved only in the Avialae, and these two points suggested that the ancestral dromaeosaurid could not glide or fly. Based on this cladistic analysis, Mahakala suggests that the ancestral condition for dromaeosaurids is non-flying.
Phylogeny and taxonomy[change | change source]
Dromaeosauridae was first defined as a clade by Paul Sereno in 1998, as the most inclusive natural group containing Dromaeosaurus but not Troodon, Ornithomimus or Passer. The various "subfamilies" have also been re-defined as clades.
The subfamilies of Dromaeosauridae is not yet settled. Mahakala, for example, the most primitive dromaeosaur in terms of structure, falls outside any named sub-group. The most basal subfamily of dromaeosaurs is often found to be the Unenlagiinae.
All known dromaeosaur skin impressions come from this group, and all show an extensive covering of feathers and well-developed wings. Some species may have been capable of active flight.
The following classification of the various genera of dromaeosaurids is based on studies by Sereno (2005), Senter (2004), Makovicky et al. (2005), Norell et al. (2006), and Turner et al. (2007).
- Family Dromaeosauridae
- Subfamily Dromaeosaurinae
- Subfamily Microraptorinae
- Subfamily Saurornitholestinae
- Subfamily Unenlagiinae
- Subfamily Velociraptorinae Velociraptorinae is a subfamily of the Dromaeosauridae. It existed from the Late Jurassic period to the end of the Cretaceous period. The Velociraptorinae consists of Velociraptor, Deinonychus, Tsaagan, Saurornitholestes, and Balaur. Teeth belonging to a giant velociraptorine the size of Utahraptor have also been reported from the Isle of Wight, England.
In general, velociraptorines tend to have longer, narrower jaws and more slender bodily proportions than the dromaeosaurines.
In popular culture[change | change source]
A Deinonychus appears in John Brosnan's 1984 novel Carnosaur and its movie adaptation though the book itself received little press attention.
Velociraptor, a dromaeosaur, got attention after it was featured in the 1993 Steven Spielberg movie Jurassic Park. However, the size of the Velociraptor in the movie is much larger than the largest members of that genus. Robert Bakker recalled that Spielberg had been disappointed with the dimensions of Velociraptor and so upsized it, adding that soon afterwards he named Utahraptor which was more the size depicted, or larger.
Michael Crichton used the name Velociraptor for the much larger raptor in his novels, on which the first two movies were based. The depiction of the dromaeosaur in the original Jurassic Park movie, while accurate for its time, is now known to have been inaccurate in some respects, such as the lack of feathers. While Jurassic Park III attempted to address this last oversight by adding quill-like structures around the head of some of its dromaeosaurs, they did not resemble the structure or distribution of actual dromaeosaurid feathers known from fossil remains.
Dromaeosaurids also appear in many of The Land Before Time movies, beginning with the third.
References[change | change source]
- Acorn J. (2007). Deep Alberta: fossil facts and dinosaur digs. University of Alberta Press. pp. 13. ISBN 0888644817.
- Case J.A. Martin J.E. and Reguero M. 2007. A dromaeosaur from the Maastrichtian of James Ross Island and the Late Cretaceous Antarctic dinosaur fauna. Pp. 1–4 in Cooper A. Raymond C. and Team I.E. (eds), Antarctica: a keystone in a changing world. Online Proceedings for the Tenth International Symposium on Antarctic Earth Sciences, U.S. Geological Survey Open-File Report 2007-1047, SRP 083. U.S. Geological Survey, Washington D.C.
- Metcalf S.J. et al (1992). "A new Bathonian (Middle Jurassic) microvertebrate site, within the Chipping Norton Limestone Formation at Hornsleaslow Quarry, Gloucestershire". Proceedings of the Geologists’ Association 103: 321–342. doi:10.1016/S0016-7878(08)80129-0.
- Makovicky, Peter J., Apesteguía, Sebastián & Agnolín, Federico L. 2005. The earliest dromaeosaurid theropod from South America. Nature, 437: 1007–1011. doi:10.1038/nature03996
- Norell M.A. and Makovicky P.J. (2004). "Dromaeosauridae". In Weishampel D.B. Dodson P. Osmólska H.. The Dinosauria (2nd ed.). Berkeley: University of California Press. pp. 196–210. ISBN 0-520-24209-2.
- Li et al, Rihui (2007). "Behavioral and faunal implications of Early Cretaceous deinonychosaur trackways from China". Naturwissenschaften. http://www.springerlink.com/content/v1u455854212404r/.
- Z. et al, Csiki (2010). "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 preprint (35): 15357–61. doi:10.1073/pnas.1006970107. PMC 2932599. PMID 20805514. Supporting Information
- Ostrom, J. H. (1969). "Osteology of Deinonychus antirrhopus, an unusual theropod from the Lower Cretaceous of Montana". Peabody Museum of Natural History Bulletin 30: 1–165.
- Norell, Mark A.; & Makovicky, Peter J. (1999). "Important features of the dromaeosaurid skeleton II: information from newly collected specimens of Velociraptor mongoliensis". American Museum Novitates 3282: 1–45. http://hdl.handle.net/2246/3025.
- Chatterjee S. and Templin R.J. 2007. Biplane wing planform and flight performance of the feathered dinosaur Microraptor gui. Proceedings of the National Academy of Sciences, 104(5): 1576–1580. 
- Hwang S.H. Norell M.A. Ji Q. and Gao K. 2002. "New Specimens of Microraptor zhaoianus (Theropoda: Dromaeosauridae) from Northeastern China." American Museum Novitates, 3381: 44pp.al.2002.pdf
- Perle A. Norell M.A. and Clark J. 1999. A new maniraptoran theropod - Achillobator giganticus (Dromaeosauridae) - from the Upper Cretaceous of Burkhant, Mongolia. Contributions of the Mongolian-American Paleontological Project, 101: 1–105.
- Britt et al 2001. New osteological data and the affinities of Utahraptor from the Cedar Mountain Fm. (Early Cretaceous) of Utah. Journal of Vertebrate Paleontology, 21(3): 36A.
- Naish, D. Hutt, and Martill D.M. 2001. Saurischian dinosaurs: theropods. in Martill D.M. and Naish D. (eds). Dinosaurs of the Isle of Wight. The Palaeontological Association, Field Guides to Fossils. 10, 242-309.
- Turner, A.S.; Hwang S.H.; and Norell M.A. (2007). "A small derived theropod from Öösh, Early Cretaceous, Baykhangor Mongolia" (PDF). American Museum Novitates 3557: 1–27. doi:10.1206/0003-0082(2007)3557[1:ASDTFS]2.0.CO;2. http://digitallibrary.amnh.org/dspace/bitstream/2246/5845/1/N3557.pdf. Retrieved 2007-03-29.
- Xing, Xu; et al. (2003). "Four-winged dinosaurs from China". Nature 421 (6921): 335–340. doi:10.1038/nature01342. PMID 12540892.
- Xu X. Wang X.-L. and Wu X.-C. (1999). "A dromaeosaur dinosaur with a filamentous integument from the Yixian Formation of China". Nature 401: 262–266. doi:10.1038/45769.
- Turner, A.H.; Makovicky P.J.; and Norell M.A. (2007). "Feather quill knobs in the dinosaur Velociraptor" (pdf). Science 317 (5845): 1721. doi:10.1126/science.1145076. PMID 17885130. http://www.sciencemag.org/cgi/reprint/317/5845/1721.pdf.
- Paul, Gregory S. 2002. Dinosaurs of the Air: the evolution and loss of flight in dinosaurs and birds. Baltimore: Johns Hopkins University Press. 472 pp.
- Prum R. and Brush A.H. 2002. The evolutionary origin and diversification of feathers. The Quarterly Review of Biology, 77: 261–295.
- Adams, Dawn (1987) "The bigger they are, the harder they fall: Implications of ischial curvature in ceratopsian dinosaurs" pg 1–6 in Currie, Philip J. and Koster, E. (eds) Fourth symposium on mesozoic terrestrial ecosystems. Tyrrell Museum, Drumheller, Canada
- Manning P.L. et al (2005). "Dinosaur killer claws or climbing crampons?". Biology Letters 2 (1): 110–112. doi:10.1098/rsbl.2005.0395. PMC 1617199. PMID 17148340. http://www.journals.royalsoc.ac.uk/openurl.asp?genre=article&eissn=1744-957X&volume=2&issue=1&spage=110.
- Davies S.J.J.F. 2002. Ratites and Tinamous Oxford University Press. New York, USA
- Redford, Kent H. Peters, Gustav. 1986. Notes on the biology and song of the red-legged seriema (cariama cristata) Journal of Field Ornithology, 57, 261–269.
- Manning P.L. et al 2009. Biomechanics of dromaeosaurid dinosaur claws: Application of X-ray microtomography, nanoindentation, and finite element analysis. The Anatomical Record: Advances in Integrative Anatomy and Evolutionary Biology, 292(9): 1397-1405.
- "Velociraptor's 'killing' claws were for climbing". New Scientist (2725). September 2009. https://www.newscientist.com/article/mg20327254.100-velociraptors-killing-claws-were-for-climbing.html. Retrieved 2009-09-15.
- Maxwell, W. D.; Ostrom, J.H. (1995). "Taphonomy and paleobiological implications of Tenontosaurus-Deinonychus associations". Journal of Vertebrate Paleontology 15 (4): 707–712. doi:10.1080/02724634.1995.10011256.
- Makovicky, Peter J. et al 2005. The earliest dromaeosaurid theropod from South America. Nature, 437: 1007–1011. doi:10.1038/nature03996
- Norell M.A. et al 2006. A new dromaeosaurid theropod from Ukhaa Tolgod (Omnogov, Mongolia). American Museum Novitates, 3545: 1–51.
- Forster, Catherine A. et al (1998a). "The theropod ancestry of birds: new evidence from the late Cretaceous of Madagascar". Science 279 (5358): 1915–1919. doi:10.1126/science.279.5358.1915.. (HTML abstract).
- Chiappe, L.M.. Glorified dinosaurs: The origin and early evolution of birds. Sydney: UNSW Press.
- Norell M. Clark J.M., Makovicky P.J. 2001. "Phylogenetic relationships among coelurosaurian theropods." New Perspectives on the Origin and Evolution of Birds: Proceedings of the International Symposium in Honor of John H. Ostrom”, Yale Peabody Museum: 49–67.
- Senter, Phil et al 2004. Systematics and evolution of Dromaeosauridae (Dinosauria, Theropoda). Bulletin of the Gunma Museum of Natural History 8: 1–20.
- Padian K. and Dial K.P. 2005. Could 'four-winged' dinosaurs fly? Nature, 438 17 November 2005: E3. doi:0.1038/nature04354
- Olshevsky, George. 1994. The birds first? A theory to fit the facts — evolution of reptiles into birds. Omni, June 1994. Volume 16 No. 9
- Martin L.S. 2004. A basal archosaurian origin for birds. Acta Geologica Sinica, 50(6): 978–990.
- Turner Alan H. et al (2007). "A basal dromaeosaurid and size evolution preceding avian flight" (pdf). Science 317 (5843): 1378–1381. doi:10.1126/science.1144066. PMID 17823350. http://www.sciencemag.org/cgi/reprint/317/5843/1378.pdf.
- Matthew W.D. and Brown B. 1922. The family Deinodontidae, with notice of a new genus from the Cretaceous of Alberta. Bulletin of the American Museum of Natural History, 46: 367–385.
- Sereno P.C. 2005. Stem Archosauria—TaxonSearch [version 1.0, November 7, 2005
- Longrich, N.R. and Currie, P.J. 2009. A microraptorine (Dinosauria–Dromaeosauridae) from the Late Cretaceous of North America. Proceedings of the National Academy of Sciences, online preprint 16 March 2009.
- Bonaparte, (1999).
- Novas F.E. et al 2008. A bizarre Cretaceous theropod dinosaur from Patagonia and the evolution of Gondwanan dromaeosaurids. Proceedings of the Royal Society B, doi:10.1098/rspb.2008.1554
- Barsbold, R. (1983). "O ptich'ikh chertakh v stroyenii khishchnykh dinozavrov. ["Avian" features in the morphology of predatory dinosaurs]." Transactions of the Joint Soviet Mongolian Paleontological Expedition 24: 96–103. [Original article in Russian.] Translated by W. Robert Welsh, copy provided by Kenneth Carpenter and converted by Matthew Carrano. PDF fulltext
- "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 preprint (35): 15357–61. doi:10.1073/pnas.1006970107. PMC 2932599. PMID 20805514. Supporting Information
- Sweetman, S.C. (2004). "The first record of velociraptorine dinosaurs (Saurischia, Theropoda) from the Wealden (Early Cretaceous, Barremian) of southern England." Cretaceous Research, 25(3): 353–364. doi:10.1016/j.cretres.2004.01.004
- Bakker, Robert T. (1995). Raptor Red. New York: Bantam Books. pp. 4. ISBN 0-553-57561-9.
Other websites[change | change source]
|Wikispecies has information on: Dromaeosauridae.|
|Wikimedia Commons has media related to Dromaeosauridae.|
- Dromaeosauridae at DinoData.
- The Dromaeosauridae: The Raptors!, from the University of California Berkeley Museum of Paleontology.
- Dromaeosauridae, by Justin Tweet from Thescelosaurus.
- Dinosaurs – Complete and free online edition of the book "Dinosaurs" as written by W. D. Matthew (cited in this article with authorship of the family Dromaeosauridae), and former Curator of Vertebrate Paleontology at the American Museum of Natural History in New York; Originally published in 1915
- Dromaeosauridae, Dinosaur-world reference with in-depth description and pictures of many dromaeosauridae dinosaurs