Temporal range: Middle Jurassic – Late Cretaceous, 164–65.5Ma
|Deinonychus antirrhopus (large) and Buitreraptor gonzalezorum (small), Field Museum of Natural History|
Matthew & Brown, 1922
Matthew & Brown, 1922
Matthew & Brown, 1922
Ornithodesmidae Hooley, 1913
Dromaeosauridae is a family of bird-like theropod dinosaurs. They were small- to medium-sized feathered carnivores that flourished in the Cretaceous Period. The name Dromaeosauridae means 'running lizards', from Greek dromeus (δρομευς) meaning 'runner' and sauros (σαυρος) meaning 'lizard'. In informal usage they are often called raptors (after Velociraptor), a term popularized by the film Jurassic Park; a few types include the term "raptor" directly in their name and have come to emphasize their supposed bird-like habits.
Dromaeosaurid fossils have been found in North America, Europe, Africa, Japan, China, Mongolia, Madagascar, Argentina, and Antarctica. They first appeared in the mid-Jurassic Period (late Bathonian stage, about 164 million years ago) and survived until the end of the Cretaceous (Maastrichtian stage, 65.5 ma), existing for over 100 million years, up until the Cretaceous–Paleogene extinction event. The presence of dromaeosaurs as early as the Middle Jurassic has been confirmed by the discovery of isolated fossil teeth, though no dromaeosaurid body fossils have been found from this period.
The distinctive dromaeosaurid body plan helped to rekindle theories that at least some dinosaurs may have been active, fast, and closely related to birds. Robert Bakker’s illustration for John Ostrom’s 1969 monograph, showing the dromaeosaurid Deinonychus in a fast run, is among the most influential paleontological reconstructions in history. The dromaeosaurid body plan includes a relatively large skull, serrated teeth, narrow snout, and forward-facing eyes which indicate some degree of binocular vision. Dromaeosaurids, like most other theropods, had a moderately long S-curved neck, and their trunk was relatively short and deep. Like other maniraptorans, they had long arms that could be folded against the body in some species, and relatively large hands with three long fingers (the middle finger being the longest and the first finger being the shortest) ending in large claws. The dromaeosaurid hip structure featured a characteristically large pubic boot projecting beneath the base of the tail. Dromaeosaurid feet bore a large, recurved claw on the second toe. Their tails were slender, with long, low, vertebrae lacking transverse process and neural spines after the 14th caudal vertebra.
It is now known that at least some, and probably all, dromaeosaurids were covered in feathers, including large, vaned, wing and tail feathers. This development, first hypothesized in the mid-late 1980s and confirmed by fossil discoveries in 1999, represents a significant change in the way dromaeosaurids have historically been depicted in art and film (see “Feathers” below).
Like other theropods, dromaeosaurids were bipedal; that is, they walked on their hind legs. However, whereas most theropods walked with three toes contacting the ground, fossilized footprint tracks confirm that most deinonychosaurs, including the dromaeosaurids, 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. The enlarged second toe bore an unusually large, curved sickle-shaped claw (held off the ground or 'retracted' when walking), which is thought to have been used in capturing prey and climbing trees (see "Claw function" below). This claw was especially blade-like in the large-bodied predatory eudromaeosaurs. One eudromaeosaur species, Balaur bondoc, also 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 also held retracted and bore enlarged, sickle-shaped claws.
Dromaeosaurids 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 that is curved horizontally in a long S-shape. This suggests that, in life, the tail could bend from side to side with a substantial degree of flexibility. It has been proposed that this tail was used as a stabilizer and/or counterweight while running or in the air; in Microraptor, an elongate diamond-shaped fan of feathers is preserved on the end of the tail. This may have been used as an aerodynamic stabilizer and rudder during gliding and/or powered flight (see "Flight and gliding" below).
Dromaeosaurids were small to medium-sized dinosaurs, ranging from about 0.7 metres (2.3 ft) in length (in the case of Mahakala) to over 6 metres (20 ft) (in Utahraptor and Achillobator). Some may have grown larger; undescribed specimens of Utahraptor in Brigham Young University collections belonged to individuals that may have reached up to 11 m (36 ft) long, though these await more detailed study. Large size appears to have evolved at least twice among dromaeosaurids; once among the dromaeosaurines Utahraptor and Achillobator, and again among the unenlagiines (Austroraptor, which measured 5 metres (16 ft) long). A possible third lineage of giant dromaeosaurs is represented by isolated teeth found on the Isle of Wight, England. The teeth belong to an animal the size of the dromaeosaurine Utahraptor, but they appear to belong to velociraptorines, judging by the shape of the teeth.
Mahakala is both the most primitive dromaeosaurid ever described and the smallest. This evidence, combined with the small size of other primitive relatives such as Microraptor and the troodontid Anchiornis, indicates that the common ancestor of dromaeosaurids, troodontids, and birds (which is called the ancestral paravian) may have been very small, at around 65 cm in length and 600 to 700 grams of mass.
There is a large body of evidence showing that dromaeosaurids were covered in feathers. Some dromaeosaurid fossils preserve long, pennaceous 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.
The first known dromaeosaur with definitive evidence of feathers was Sinornithosaurus, reported from China by Xu et al. in 1999. Many other dromaeosaurid 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 dromaeosaurids bore feathers, since even flightless birds today retain most of their plumage, and relatively large dromaeosaurids, like Velociraptor, are known to have retained pennaceous feathers. Though some scientists had suggested that the larger dromaeosaurids lost some or all of their insulatory covering, the discovery of feathers in Velociraptor specimens has been cited as evidence that all members of the family retained feathers.
There is currently disagreement 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 dromaeosaurids. However, Manning et al. argued that the claw instead served as a hook, reconstructing the keratinous sheath with an elliptical cross section, instead of the previously inferred inverted teardrop shape. 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. Ostrom cited Gilliard (1958) in saying that they can sever an arm or disembowel a man. Kofron (1999 and 2003) studied 241 documented cassowary attacks and found that one human and two dogs had been killed, but no evidence that cassowaries can disembowel or dismember other animals. Cassowaries use their claws to defend themselves, to attack threatening animals, and in agonistic displays such as the Bowed Threat Display. The seriema also has an enlarged second toe claw, and uses it to tear apart small prey items for swallowing.
Phillip Manning and colleagues (2009) attempted to test the function of the sickle claw and similarly shaped claws on the forelimbs. They analyzed the bio-mechanics of how stresses and strains would be distributed along the claws and into the limbs, using X-ray imaging to create a three dimensional contour map of a forelimb claw from Velociraptor. For comparison, they analyzed the construction of a claw from a modern predatory bird, the Eagle Owl. They found that, based on the way that stress was conducted along the claw, they were ideal for climbing. The scientists found that the sharpened tip of the claw was a puncturing and gripping instrument, while the curved and expanded claw base helped transfer stress loads evenly.
The Manning team also compared the curvature of the dromaeosaurid "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 commented on the Manning team's study, stating 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. Mackovickey speculated that giant dromaeosaurids may have adapted the claw to be used exclusively for latching on to prey.
In 2009 Phil Senter published a study on dromaeosaurid toes and showed that their range of motion was compatible with the excavation of tough insect nests. Senter suggested that small dromaeosaurids such as Rahonavis and Buitreraptor were small enough to be partial insectivores, while larger genera such as Deinonychus and Neuquenraptor could have used this ability to catch vertebrate prey residing in insect nests. However, Senter did not test whether the strong curvature of dromaeosaurid claws was also conductive to such activities.
In 2011, Denver Fowler and colleagues suggested a new method by which dromaeosaurs may have taken smaller prey. This model, known as the "raptor prey restraint" (RPR) model of predation, proposes that dromaeosaurs killed their prey in a manner very similar to extant accipitrid birds of prey: by leaping onto their quarry, pinning it under their body weight, and gripping it tightly with the large, sickle-shaped claws. Like accipitrids, the dromaeosaur would then begin to feed on the animal while still alive, until it eventually died from blood loss and organ failure. This proposal is based primarily on comparisons between the morphology and proportions of the feet and legs of dromaeosaurs to several groups of extant birds of prey with known predatory behaviors. Fowler found that the feet and legs of dromaeosaurs most closely resemble those of eagles and hawks, especially in terms of having an enlarged second claw and a similar range of grasping motion. The short metatarsus and foot strength, however, would have been more similar to that of owls. The RPR method of predation would be consistent with other aspects of dromaeosaurid anatomy, such as their unusual dentition and arm morphology. The arms, which could exert a lot of force but were likely covered in long feathers, may have been used as flapping stabilizers for balance while atop a struggling prey animal, along with the stiff counterbalancing tail. Dromaeosaurid jaws, thought by Fowler and colleagues to be comparatively weak, would have been useful for eating prey alive but not as useful for quick, forceful dispatch of the prey. These predatory adaptations working together may also have implications for the origin of flapping in paravians.
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 subsequent study published in 2007 by Roach and Brinkman suggests that the Deinonychus may have actually displayed a disorganized mobbing behavior. Modern diapsids, including birds and crocodiles (the closest relatives of dromaeosaurs), display minimal cooperative hunting; instead, they are usually either solitary hunters, or are drawn to previously killed carcasses, where conflict often occurs between individuals of the same species. For example, in situations where groups of komodo dragons are eating together, the largest individuals eat first and might attack smaller komodo dragons that attempt to feed; if the smaller animal dies, it is usually cannibalized. When this information is applied to the sites containing putative pack-hunting behavior in dromaeosaurs, it appears somewhat consistent with a komodo- or crocodile-like feeding strategy. Deinonychus skeletal remains found at these sites are from subadults, with missing parts that may have been eaten by other Deinonychus, which a study by Roach et al. presented as evidence against the idea that the animals cooperated in the hunt.
In 2007, scientists described the first known extensive dromaeosaur trackway, in Shandong, China. In addition to confirming the hypothesis that the sickle-claw was held retracted off the ground, the trackway (made by a large, Achillobator-sized species) showed evidence of six individuals of about equal size moving 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 authors of the paper describing these footprints interpreted the trackways as 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, according to the authors, could not be ruled out.
Flying and gliding
The ability to fly or glide has been suggested for at least two dromaeosaurid species. The first, Rahonavis ostromi (originally classified as avian bird, but found to be a dromaeosaurid in later studies) may have been capable of powered flight, as indicated by its long forelimbs with evidence of quill knob attachments for long sturdy flight feathers. 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 dromaeosaurid, Microraptor gui, 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 phugoid 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.
Comparisons between the scleral rings of several dromaeosaurids (Microraptor, Sinornithosaurus, and Velociraptor) and modern birds and reptiles indicate that some dromaeosaurids (including Microraptor and Velociraptor) may have been nocturnal predators, while Sinornithosaurus is inferred to be cathemeral (active throughout the day at short intervals). However, the discovery of iridescent plumage in Microraptor has cast doubt on the inference of nocturnality in this genus, as no modern birds that have iridescent plumage are known to be nocturnal.
Studies of the olfactory bulbs of dromaeosaurids reveal that they had similar olfactory ratios for their size to other non-avian theropods and modern birds with an acute sense of smell, such as tyrannosaurids and the Turkey Vulture, probably reflecting the importance of the olfactory sense in the daily activities of dromaeosaurids such as finding food.
In 2001, Bruce Rothschild and others published a study examining evidence for stress fractures and tendon avulsions in theropod dinosaurs and the implications for their behavior. Since stress fractures are caused by repeated trauma rather than singular events they are more likely to be caused by regular behavior than other types of injuries. The researchers found lesion like those caused by stress fractures on a dromaeosaurid hand claw, one of only two such claw lesions discovered in the course of the study. Stress fractures in the hands have special behavioral significance compared to those found in the feet since stress fractures there can be obtained while running or during migration. Hand injuries, by contrast, are more likely to be obtained while in contact with struggling prey.
Relationship with birds
Dromaeosaurids share many features with early birds (clade Avialae or Aves). The precise nature of their relationship to birds has undergone a great deal of study, and hypotheses about that relationship have changed as large amounts of new evidence became available. As late as 2001, Mark Norell and colleagues analyzed a large survey of coelurosaur fossils and produced the tentative result that dromaeosaurids were most closely related to birds, with troodontids as a more distant outgroup. They even suggested that Dromaeosauridae could be paraphyletic relative to Avialae. In 2002, Hwang and colleagues utilized the work of Norell et al., including new characters and better fossil evidence, to determine that birds (avialans) were better thought of as cousins to the dromaeosaurids and troodontids.
The current consensus among paleontologists agrees with the findings of Hwang et al. (2002); 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 determine whether any dromaeosaurs could fly or glide, or whether they evolved from ancestors that could.
Alternative theories and flightlessness
Dromaeosaurids are so birdlike that they have led some researchers to argue that they would be better classified as birds. First, since they had feathers, dromaeosaurs (along with many other coelurosaurian theropod dinosaurs) are “birds” under traditional definitions of the word “bird”, or “Aves”, that are based on the possession of feathers. However, other scientists, such as Lawrence Witmer, have argued that calling a theropod like Caudipteryx a bird because it has feathers may stretch the word past any useful meaning. (See the article Avialae for a discussion about the definitions of the clades Aves and Avialae.)
At least two schools of researchers have proposed that dromaeosaurs may actually be descended from flying ancestors. Hypotheses involving a flying ancestor for dromaeosaurs are sometimes called “Birds Came First” (BCF). George Olshevsky is usually credited as the first author of BCF. In his own work, Gregory S. Paul pointed out numerous features of the dromaeosaurid skeleton that he interpreted as evidence that the entire group had evolved from flying, dinosaurian, ancestors, perhaps something like Archaeopteryx. In that case, the larger dromaeosaurids were secondarily flightless, like the modern ostrich. In 1988, Paul suggested that dromaeosaurids may actually be more closely related to modern birds than to Archaeopteryx. By 2002, however, Paul placed dromaeosaurs and Archaeopteryx as the closest relatives to one another.
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.
Also in 2002, Steven Czerkas described Cryptovolans, though it is a probable junior synonym of Microraptor. He reconstructed the fossil inaccurately with only two wings and thus argued that dromaeosaurs were proper birds, rather than possible gliders. He later issued a revised reconstruction in agreement with that of Microraptor
Other 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.
In 2005, Mayr and Peters described the anatomy of a very well preserved specimen of Archaeopteryx, and determined that its anatomy was more like non-avian theropods than previously understood. Specifically, they found that Archaeopteryx had a primitive palatine, unreversed hallux, and hyper-extendable second toe. Their phylogenetic analysis produced the controversial result that Confuciusornis was closer to Microraptor than to Archaeopteryx, making the Avialae a paraphyletic taxon. They also suggested that the ancestral paravian was able to fly or glide, and that the dromaeosaurs and troodontids were secondarily flightless (or had lost the ability to glide). Corfe and Butler criticized this work on methodological grounds.
A challenge to all of these alternative scenarios came when Turner and colleagues in 2007 described a new dromaeosaurid, 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-volant. However in 2012, an expanded and revised study incorporating the most recent Dromaeosaurid finds recovered the Archaeopteryx-like Xiaotingia as the most primitive member of the clade Dromaeosauridae, which appears to suggest the earliest members of the clade may have been capable of flight.
The authorship of the family Dromaeosauridae is credited to William Diller Matthew and Barnum Brown, who erected it as a subfamily (Dromaeosaurinae) of the family Deinodontidae in 1922, containing only the new genus Dromaeosaurus. Dromaeosauridae, along with Troodontidae, make up the infraorder Deinonychosauria.
The subfamilies of Dromaeosauridae frequently shift in content based on new analysis, but typically consist of the following groups. A number of dromaeosaurids have not been assigned to any particular subfamily, often because they are too poorly preserved to be placed confidently in phylogenetic analysis (see section Phylogeny below), or because they are basal relative to the primary subdivisions of Dromaeosauridae (Mahakala, for example, is the most primitive known dromaeosaurid and falls outside any named sub-group). The most basal subfamily of dromaeosaurids is often found to be the Unenlagiinae. This enigmatic group is the most poorly supported subfamily of dromaeosaurs and it is possible that some or all of its members belong outside of Dromaeosauridae. The larger, ground-dwelling members like Buitreraptor and Unenlagia show strong flight adaptations, although they were probably too large to 'take off'. One member of this group, Rahonavis, is very small, with well-developed wings that show evidence of quill knobs (the attachment points for flight feathers) and it is very likely that it could fly. The next most primitive clade of dromaeosaurs is the Microraptoria. This group includes many of the smallest dromaeosaurs, which show adaptations for living in trees. All known dromaeosaur skin impressions hail from this group and all show an extensive covering of feathers and well-developed wings. Like the unenlagiines, some species may have been capable of active flight. The subfamily Velociraptorinae has traditionally included Velociraptor, Deinonychus, and Saurornitholestes, and while the discovery of Tsaagan lent support to this grouping, the inclusion of Saurornitholestes is still uncertain. The Dromaeosaurinae is usually found to consist of medium to giant-sized species, with generally box-shaped skulls (the other subfamilies generally have narrower snouts).
The following classification of the various genera of dromaeosaurids follows the table provided in Holtz, 2011 unless otherwise noted.
- Family Dromaeosauridae
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, usually defined as all species closer to the groups namesake than to Dromaeosaurus or any namesakes of other sub-clades (for example, Makovicky defined the clade Unenlagiinae as all dromaeosaurids closer to Unenlagia than to Velociraptor). The Microraptoria is the only dromaeosaurid sub-clade not converted from a subfamily. Senter and colleagues expressly coined the name without the subfamily suffix -inae to avoid perceived issues with erecting a traditional family-group taxon, should the group be found to lie outside dromaeosauridae proper. Sereno offered a revised definition of the sub-group containing Microraptor to ensure that it would fall within Dromaeosauridae, and erected the subfamily Microraptorinae, attributing it to Senter et al., though this usage has only appeared on his online TaxonSearch database and has not been formally published.
The cladogram below follows a 2012 analysis by paleontologists Phil Senter, James I. Kirkland, Donald D. DeBlieux, Scott Madsen and Natalie Toth.
Dromaeosaurs are diagnosed by the following features; short T-shaped frontals that form the rostral boundary of the supratemporal fenestra; a caudolateral overhanging shelf of the squamosal; a lateral process of the quadrate that contacts the quadratojugal; raised, stalked, parapophyses on the dorsal vertebrae, a modified pedal digit II; chevrons and prezygapophyses of the caudal vertebrae elongate and spanning several vertebrae; the presence of a subglenoid fossa on the coracoid.
In popular culture
Velociraptor, a dromaeosaurid, gained much attention after it was featured prominently in the 1993 Steven Spielberg film Jurassic Park. However, the dimensions of the Velociraptor in the film are 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. Gregory S. Paul, in his book Predatory Dinosaurs of the World, considered Deinonychus antirrhopus a species of Velociraptor, and so rechristened the species Velociraptor antirrhopus. This taxonomic opinion has not been widely followed.
- Senter P., Kirkland J.I., DeBlieux D.D., Madsen S., Toth N. (2012). "New Dromaeosaurids (Dinosauria: Theropoda) from the Lower Cretaceous of Utah, and the Evolution of the Dromaeosaurid Tail". PLoS ONE 7 (5): e36790. Bibcode:2012PLoSO...7E6790S. doi:10.1371/journal.pone.0036790.
- Holtz, Thomas R. Jr. (2012) Dinosaurs: The Most Complete, Up-to-Date Encyclopedia for Dinosaur Lovers of All Ages, Winter 2011 Appendix.
- Acorn, J. (2007). Deep Alberta: Fossil Facts and Dinosaur Digs. University of Alberta Press. p. 13. ISBN 0-88864-481-7.
- 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., Vaughan, R.F., Benton, M.J., Cole, J., Simms, M.J. and Dartnall, D.L. (1992). "A new Bathonian (Middle Jurassic) microvertebrate site, within the Chipping Norton Limestone Formation at Hornsleaslow Quarry, Gloucestershire". Proceedings of the Geologists' Association 103 (4): 321–342. doi:10.1016/S0016-7878(08)80129-0.
- Ostrom, J. H. (1969). "Osteology of Deinonychus antirrhopus, an unusual theropod from the Lower Cretaceous of Montana" (PDF). Peabody Museum of Natural History Bulletin 30: 1–165.
- Paul, Gregory S. (2006) "Drawing Dinosaurs"(2006). "Geotimes", January 2006. http://www.geotimes.org/jan06/feature_drawingdinos.html
- Makovicky, Peter J.; Apesteguía, Sebastián; Agnolín, Federico L. (2005). "The earliest dromaeosaurid theropod from South America". Nature 437 (7061): 1007–1011. Bibcode:2005Natur.437.1007M. doi:10.1038/nature03996. PMID 16222297.
- 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, 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. Bibcode:2008NW.....95..185L. doi:10.1007/s00114-007-0310-7. PMID 17952398.
- Longrich, N.R.; Currie, P.J. (2009). "A microraptorine (Dinosauria–Dromaeosauridae) from the Late Cretaceous of North America". PNAS 106 (13): 5002–7. Bibcode:2009PNAS..106.5002L. doi:10.1073/pnas.0811664106. PMC 2664043. PMID 19289829.
- Z., Csiki; Vremir, M.; Brusatte, S. L.; and Norell, M. A. (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 107 (35): 15357–61. Bibcode:2010PNAS..10715357C. doi:10.1073/pnas.1006970107. PMC 2932599. PMID 20805514. Supporting Information
- 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. hdl:2246/3025.
- Chatterjee, S.; 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. Bibcode:2007PNAS..104.1576C. doi:10.1073/pnas.0609975104. PMC 1780066. PMID 17242354.
- Hwang, S.H.; Norell, M.A.; Ji, Q.; Gao, K. (2002). "New Specimens of Microraptor zhaoianus (Theropoda: Dromaeosauridae) from Northeastern China". American Museum Novitates (3381): 44pp. hdl:2246/2870.
- Perle, A.; Norell, M.A.; 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; Chure; Stadtman; Madsen; Scheetz; Burge (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. doi:10.1080/02724634.2001.10010852.
- 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. 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 dromaeosaurid dinosaur with a filamentous integument from the Yixian Formation of China". Nature 401 (6750): 262–266. Bibcode:1999Natur.401..262X. 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. Bibcode:2007Sci...317.1721T. doi:10.1126/science.1145076. PMID 17885130.
- 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.; Brush, A.H. (2002). "The evolutionary origin and diversification of feathers". The Quarterly Review of Biology 77 (3): 261–295. doi:10.1086/341993. PMID 12365352.
- 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., Payne, D., Pennicott, J., Barrett, P.M., and Ennos, R.A. (2005). "Dinosaur killer claws or climbing crampons?". Biology Letters 2 (1): 110–112. doi:10.1098/rsbl.2005.0395. PMC 1617199. PMID 17148340.
- Davies, S.J.J.F. (2002) "Ratites and Tinamous" Oxford University Press. New York, USA
- Gilliard, E. T. (1958) "Living birds of the world" Doubleday, garden City, NY. USA. 400p.
- Kofron, Christopher P. (1999). "Attacks to humans and domestic animals by the southern cassowary (Casuarius casuarius johnsonii) in Queensland, Australia". Journal of Zoology 249 (4): 375–381. doi:10.1111/j.1469-7998.1999.tb01206.x.
- Kofron, Christopher P. (2003). "Case histories of attacks by the southern cassowary in Queensland". Memoirs of the Queensland Museum 49 (1): 335–338.
- Redford, Kent H.; Peters, Gustav (1986). "Notes on the biology and song of the red-legged seriema (cariama cristata)". Journal of Field Ornithology 57 (4): 261–269. JSTOR 4513154.
- Manning, P.L.; Margetts, L.; Johnson, M.R.; Withers, P.J.; Sellers, W.I.; Falkingham, P.L.; Mummery, P.M.; Barrett, P.M. 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. doi:10.1002/ar.20986.
- "Velociraptor's 'killing' claws were for climbing". New Scientist (2725). September 2009. Retrieved 2009-09-15.
- Senter, P. (2009). "Pedal function in deinonychosaurs (Dinosauria: Theropoda): a comparative study". Bulletin of the Gunma Museum of Natural History 13: 1–14.
- Fowler, D.W., Freedman, E.A., Scannella, J.B., 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. PMID 22194962.
- Choi, Charles (14 December 2011), "Velociraptors' Killer Claws Helped Them Eat Prey Alive", LiveScience
- 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.
- Roach, B. T.; D. L. Brinkman (2007). "A reevaluation of cooperative pack hunting and gregariousness in Deinonychus antirrhopus and other nonavian theropod dinosaurs". Bulletin of the Peabody Museum of Natural History 48 (1): 103–138. doi:10.3374/0079-032X(2007)48[103:AROCPH]2.0.CO;2.
- Norell, M.A.; Clark, J.M.; Turner, A.H.; Makovicky, P.J.; Barsbold, R.; Rowe, T. (2006). "A new dromaeosaurid theropod from Ukhaa Tolgod (Omnogov, Mongolia)". American Museum Novitates 3545: 1–51. doi:10.1206/0003-0082(2006)3545[1:ANDTFU]2.0.CO;2.
- Forster, Catherine A.; Sampson, Scott D.; Chiappe, Luis M. & Krause, David W. (1998a). "The Theropod Ancestry of Birds: New Evidence from the Late Cretaceous of Madagascar". Science 279 (5358): 1915–1919. Bibcode:1998Sci...279.1915F. doi:10.1126/science.279.5358.1915. PMID 9506938.. (HTML abstract).
- Chiappe, L.M. Glorified Dinosaurs: The Origin and Early Evolution of Birds. Sydney: UNSW Press. ISBN 0-471-24723-5.
- Schmitz, L.; Motani, R. (2011). "Nocturnality in Dinosaurs Inferred from Scleral Ring and Orbit Morphology". Science 332 (6030): 705–8. Bibcode:2011Sci...332..705S. doi:10.1126/science.1200043. PMID 21493820.
- Li, Quanguo (9 March 2012), "Reconstruction of Microraptor and the Evolution of Iridescent Plumage", Science 335: 1215–1219, Bibcode:2012Sci...335.1215L, doi:10.1126/science.1213780 More than one of
- Zelenitsky, D.K.; Therrien, F.; Kobayashi, Y. (2009). "Olfactory acuity in theropods: palaeobiological and evolutionary implications". Proceedings of the Royal Society B 276 (1657): 667–673. doi:10.1098/rspb.2008.1075. PMC 2660930. PMID 18957367.
- Zelenitsky, D.K.; Therrien, F.; Ridgely, R.C.; McGee, A.R.; Witmer, L.M. (2011). "Evolution of olfaction in non-avian theropod dinosaurs and birds". Proceedings of the Royal Society B. in press (1725): 3625. doi:10.1098/rspb.2011.0238.
- Rothschild, B., Tanke, D. H., and Ford, T. L., 2001, Theropod stress fractures and tendon avulsions as a clue to activity: In: Mesozoic Vertebrate Life, edited by Tanke, D. H., and Carpenter, K., Indiana University Press, p. 331-336.
- 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; Barsbold, R.; Britt, Brooks B.; Burnham, David B. (2004). "Systematics and evolution of Dromaeosauridae (Dinosauria, Theropoda)". Bulletin of the Gunma Museum of Natural History 8: 1–20.
- Padian, Kevin; Dial, Kenneth P. (2005). "Origin of flight: Could 'four-winged' dinosaurs fly?". Nature 438 (7066): E3; discussion E3–4. Bibcode:2005Natur.438E...3P. doi:10.1038/nature04354. PMID 16292258.
- Witmer, L.M. (2005) “The Debate on Avian Ancestry; Phylogeny, Function and Fossils.” In “Mesozoic Birds: Above the Heads of Dinosaurs”, pp. 3–30. ISBN 0-520-20094-2
- Olshevsky, George. (1994). "The birds first? A theory to fit the facts — evolution of reptiles into birds". Omni, June 1994. Volume 16 No. 9
- Paul, Gregory S. (1988). Predatory Dinosaurs of the World. New York: Simon and Schuster. 464 pp.
- Czerkas, S.A., Zhang, D., Li, J., and Li, Y. (2002). "Flying Dromaeosaurs", in Czerkas, S.J. (ed.): Feathered Dinosaurs and the Origin of Flight: The Dinosaur Museum Journal 1. Blanding: The Dinosaur Museum, 16–26.
- Martin, L.D. (2004). "A basal archosaurian origin for birds" (PDF). Acta Geologica Sinica 50 (6): 978–990.
- National Geographic News- Earliest Bird Had Feet Like Dinosaur, Fossil Shows – Nicholas Bakalar, December 1, 2005, Page 2. Retrieved 2006-10-18.
- Mayr, G; et al. (2005). "A Well-Preserved Archaeopteryx Specimen with Theropod Features". Science 310 (5753): 1483–1486. Bibcode:2005Sci...310.1483M. doi:10.1126/science.1120331. PMID 16322455.
- Mayr, G; Peters, SD (2006). "Response to comment on 'A Well-Preserved Archaeopteryx Specimen with Theropod Features'". Science 313 (5791): 1238c. Bibcode:2006Sci...313.1238M. doi:10.1126/science.1130964.
- Corfe, IJ; Butler, RJ (2006). "Comment on 'A Well-Preserved Archaeopteryx Specimen with Theropod Features'". Science 313 (5791): 1238b. Bibcode:2006Sci...313.1238C. doi:10.1126/science.1130800. PMID 16946054.
- Turner, Alan H.; Pol, Diego; Clarke, Julia A.; Erickson, Gregory M.; and Norell, Mark (2007). "A basal dromaeosaurid and size evolution preceding avian flight". Science 317 (5843): 1378–1381. Bibcode:2007Sci...317.1378T. doi:10.1126/science.1144066. PMID 17823350.
- Matthew, W. D.; 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. hdl:2246/1300.
- Agnolin, F.L.; Novas, F.E. (2011). "Unenlagiid theropods: are they members of the Dromaeosauridae (Theropoda, Maniraptora)?" (PDF). Anais da Academia Brasileira de Ciências 83: 117–162. doi:10.1590/S0001-37652011000100008. Retrieved 2011-04-23.
- Sereno, P. C. 2005. Stem Archosauria—TaxonSearch [version 1.0, November 7, 2005
- Turner, A. H.; Makovicky, P. J.; Norell, M. A. (2012). "A Review of Dromaeosaurid Systematics and Paravian Phylogeny". Bulletin of the American Museum of Natural History 371: 1. doi:10.1206/748.1.
- Bakker, Robert T. (1995). Raptor Red. New York: Bantam Books. p. 4. ISBN 0-553-57561-9.
- Pérez-Moreno, B.P.; J. L. Sanz, J. Sudre and B. Sigé (1994). "A theropod dinosaur from the Lower Cretaceous of southern France". Dinosaurs and Other Fossil Reptiles of Europe, Second Georges Cuvier Symposium, Montbéliard; Revue de Paléobiologie, Volume spécial 7: 173–188.
- Currie, P. J. (1995). "New information on the anatomy and relationships of Dromaeosaurus albertensis (Dinosauria: Theropoda)". Journal of Vertebrate Paleontology 15 (3): 576–591. doi:10.1080/02724634.1995.10011250. (abstract)
|Wikispecies has information related to: 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