Wikipedia

Deinonychus

This article is about the dinosaur. For the doom metal group, see Deinonychus (band).
Not to be confused with Deinocheirus or Deinosuchus.

Deinonychus (/daɪˈnɒnɪkəs/[1] dy-NON-ih-kəs; from Ancient Greek δεινός (deinós) 'terrible' and ὄνυξ (ónux), genitive ὄνυχος (ónukhos) 'claw') is a genus of dromaeosaurid theropod dinosaur with one described species, Deinonychus antirrhopus. This species, which could grow up to 3.4 meters (11 ft) long, lived during the early Cretaceous Period, about 115–108 million years ago (from the mid-Aptian to early Albian stages). Fossils have been recovered from the U.S. states of Montana, Utah, Wyoming, and Oklahoma, in rocks of the Cloverly Formation and Antlers Formation, though teeth that may belong to Deinonychus have been found much farther east in Maryland.

Deinonychus
Temporal range: Early Cretaceous (Aptian to Albian), 115–108 Ma
Mounted skeleton cast, Field Museum
Scientific classification Edit this classification
Domain: Eukaryota
Kingdom: Animalia
Phylum: Chordata
Clade: Dinosauria
Clade: Saurischia
Clade: Theropoda
Family: †Dromaeosauridae
Clade: †Eudromaeosauria
Genus: †Deinonychus
Ostrom, 1969
Type species
†Deinonychus antirrhopus
Ostrom, 1969
Synonyms

Paleontologist John Ostrom's study of Deinonychus in the late 1960s revolutionized the way scientists thought about dinosaurs, leading to the "dinosaur renaissance" and igniting the debate on whether dinosaurs were warm-blooded or cold-blooded. Before this, the popular conception of dinosaurs had been one of plodding, reptilian giants. Ostrom noted the small body, sleek, horizontal posture, ratite-like spine, and especially the enlarged raptorial claws on the feet, which suggested an active, agile predator.[2]

"Terrible claw" refers to the unusually large, sickle-shaped talon on the second toe of each hind foot. The fossil YPM 5205 preserves a large, strongly curved ungual. In life, archosaurs have a horny sheath over this bone, which extends the length. Ostrom looked at crocodile and bird claws and reconstructed the claw for YPM 5205 as over 120 millimetres (4.7 in) long.[2] The species name antirrhopus means "counter balance", which refers to Ostrom's idea about the function of the tail. As in other dromaeosaurids, the tail vertebrae have a series of ossified tendons and super-elongated bone processes. These features seemed to make the tail into a stiff counterbalance, but a fossil of the very closely related Velociraptor mongoliensis (IGM 100/986) has an articulated tail skeleton that is curved laterally in a long S-shape. This suggests that, in life, the tail could bend to the sides with a high degree of flexibility.[3] In both the Cloverly and Antlers formations, Deinonychus remains have been found closely associated with those of the ornithopod Tenontosaurus. Teeth discovered associated with Tenontosaurus specimens imply they were hunted, or at least scavenged upon, by Deinonychus.

Discovery and naming

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Fossilized remains of Deinonychus have been recovered from the Cloverly Formation of Montana and Wyoming[2] and in the roughly contemporary Antlers Formation of Oklahoma,[4] in North America. The Cloverly formation has been dated to the late Aptian through early Albian stages of the early Cretaceous, about 115 to 108 Ma.[5][6] Additionally, teeth found in the Arundel Clay Facies (mid-Aptian), of the Potomac Formation on the Atlantic Coastal Plain of Maryland may be assigned to the genus.[7]

The first remains were uncovered in 1931 in southern Montana near the town of Billings. The team leader, paleontologist Barnum Brown, was primarily concerned with excavating and preparing the remains of the ornithopod dinosaur Tenontosaurus, but in his field report from the dig site to the American Museum of Natural History, he reported the discovery of a small carnivorous dinosaur close to a Tenontosaurus skeleton, "but encased in lime difficult to prepare."[8] He informally called the animal "Daptosaurus agilis" and made preparations for describing it and having the skeleton, specimen AMNH 3015, put on display, but never finished this work.[9] Brown brought back from the Cloverly Formation the skeleton of a smaller theropod with seemingly oversized teeth that he informally named "Megadontosaurus". John Ostrom, reviewing this material decades later, realized that the teeth came from Deinonychus, but the skeleton came from a completely different animal. He named this skeleton Microvenator.[9]

 
Cast of the holotype foot YPM 5205 from two angles

A little more than thirty years later, in August 1964, paleontologist John Ostrom led an expedition from Yale's Peabody Museum of Natural History which discovered more skeletal material near Bridger. Expeditions during the following two summers uncovered more than 1,000 bones, among which were at least three individuals. Since the association between the various recovered bones was weak, making the exact number of individual animals represented impossible to determine properly, the type specimen (YPM 5205) of Deinonychus was restricted to the complete left foot and partial right foot that definitely belonged to the same individual.[10] The remaining specimens were catalogued in fifty separate entries at Yale's Peabody Museum although they could have been from as few as three individuals.[10]

Later study by Ostrom and Grant E. Meyer analyzed their own material as well as Brown's "Daptosaurus" in detail and found them to be the same species. Ostrom first published his findings in February 1969, giving all the referred remains the new name of Deinonychus antirrhopus. The specific name "antirrhopus", from Greek ἀντίρροπος, means "counterbalancing" and refers to the likely purpose of a stiffened tail.[11] In July 1969, Ostrom published a very extensive monograph on Deinonychus.[10]

Though a myriad of bones was available by 1969, many important ones were missing or hard to interpret. There were few postorbital skull elements, no femurs, no sacrum, no furcula or sternum, missing vertebrae, and (Ostrom thought) only a tiny fragment of a coracoid. Ostrom's skeletal reconstruction of Deinonychus included a very unusual pelvic bone—a pubis that was trapezoidal and flat, unlike that of other theropods, but which was the same length as the ischium and which was found right next to it.[10]

Further findings

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Specimen MCZ 4371 with skull cast at Harvard Museum of Natural History, Harvard University

In 1974, Ostrom published another monograph on the shoulder of Deinonychus in which he realized that the pubis that he had described was actually a coracoid—a shoulder element.[12] In that same year, another specimen of Deinonychus, MCZ 4371, was discovered and excavated in Montana by Steven Orzack during a Harvard University expedition headed by Farish Jenkins. This discovery added several new elements: well preserved femora, pubes, a sacrum, and better ilia, as well as elements of the pes and metatarsus. Ostrom described this specimen and revised his skeletal restoration of Deinonychus. This time it showed the very long pubis, and Ostrom began to suspect that they may have even been a little retroverted like those of birds.[13]

 
Reconstructed skeleton of specimen AMNH 3015, with outdated hand posture
 
The similarity of the forelimbs (left) with those of Archaeopteryx (right) led John Ostrom to revive the link between dinosaurs and birds

A skeleton of Deinonychus, including bones from the original (and most complete) AMNH 3015 specimen, can be seen on display at the American Museum of Natural History,[14] with another specimen (MCZ 4371) on display at the Museum of Comparative Zoology at Harvard University. The American Museum and Harvard specimens are from a different locality than the Yale specimens. Even these two skeletal mounts are lacking elements, including the sterna, sternal ribs, furcula, and gastralia.[15]

Even after all Ostrom's work, several small blocks of lime-encased material remained unprepared in storage at the American Museum. These consisted mostly of isolated bones and bone fragments, including the original matrix, or surrounding rock in which the specimens were initially buried. An examination of these unprepared blocks by Gerald Grellet-Tinner and Peter Makovicky in 2000 revealed an interesting, overlooked feature. Several long, thin bones identified on the blocks as ossified tendons (structures that helped stiffen the tail of Deinonychus) turned out to actually represent gastralia (abdominal ribs). More significantly, a large number of previously unnoticed fossilized eggshells were discovered in the rock matrix that had surrounded the original Deinonychus specimen.[16]

In a subsequent, more detailed report, on the eggshells, Grellet-Tinner and Makovicky concluded that the egg almost certainly belonged to Deinonychus, representing the first dromaeosaurid egg to be identified.[8] Moreover, the external surface of one eggshell was found in close contact with the gastralia suggesting that Deinonychus might have brooded its eggs. This implies that Deinonychus used body heat transfer as a mechanism for egg incubation, and indicates an endothermy similar to modern birds.[17] Further study by Gregory Erickson and colleagues finds that this individual was 13 or 14 years old at death and its growth had plateaued. Unlike other theropods in their study of specimens found associated with eggs or nests, it had finished growing at the time of its death.[18]

Implications

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Ostrom's description of Deinonychus in 1969 has been described as the most important single discovery of dinosaur paleontology in the mid-20th century.[19] The discovery of this clearly active, agile predator did much to change the scientific (and popular) conception of dinosaurs and opened the door to speculation that some dinosaurs may have been warm-blooded. This development has been termed the dinosaur renaissance. Several years later, Ostrom noted similarities between the forefeet of Deinonychus and that of birds, an observation which led him to revive the hypothesis that birds are descended from dinosaurs.[20] Forty years later, this idea is almost universally accepted.

Because of its extremely bird-like anatomy and close relationship to other dromaeosaurids, paleontologists hypothesize that Deinonychus was probably covered in feathers.[21][22][23] Clear fossil evidence of modern avian-style feathers exists for several related dromaeosaurids, including Velociraptor and Microraptor, though no direct evidence is yet known for Deinonychus itself.[24][25] When conducting studies of such areas as the range of motion in the forelimbs, paleontologists like Phil Senter have taken the likely presence of wing feathers (as present in all known dromaeosaurs with skin impressions) into consideration.[26]

Description

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Life restoration

Based on the few fully mature specimens,[27] Paul estimated that Deinonychus could reach 3.3–3.4 meters (10 ft 10 in – 11 ft 2 in) in length, with a skull length of 410 millimeters (16 in), a hip height of 0.87 meters (2.9 ft) and a body mass of 60–73 kg (132–161 lb).[28][29] Campione and his colleagues proposed a higher mass estimate of 100 kg (220 lb) based on femur and humerus circumference.[30] The skull was equipped with powerful jaws lined with around seventy curved, blade-like teeth. Studies of the skull have progressed a great deal over the decades. Ostrom reconstructed the partial, imperfectly preserved skulls that he had as triangular, broad, and fairly similar to Allosaurus. Additional Deinonychus skull material and closely related species found with good three-dimensional preservation[31] show that the palate was more vaulted than Ostrom thought, making the snout far narrower, while the jugals flared broadly, giving greater stereoscopic vision. The skull of Deinonychus was different from that of Velociraptor, however, in that it had a more robust skull roof, like that of Dromaeosaurus, and did not have the depressed nasals of Velociraptor.[32] Both the skull and the lower jaw had fenestrae (skull openings) which reduced the weight of the skull. In Deinonychus, the antorbital fenestra, a skull opening between the eye and nostril, was particularly large.[31]

 
Size compared with a human

Deinonychus possessed large "hands" (manus) with three claws on each forelimb. The first digit was shortest and the second was longest. Each hind foot bore a sickle-shaped claw on the second digit, which was probably used during predation.[10]

No skin impressions have ever been found in association with fossils of Deinonychus. Nonetheless, the evidence suggests that the Dromaeosauridae, including Deinonychus, had feathers.[24] The genus Microraptor is both older geologically and more primitive phylogenetically than Deinonychus, and within the same family.[33] Multiple fossils of Microraptor preserve pennaceous, vaned feathers like those of modern birds on the arms, legs, and tail, along with covert and contour feathers.[24] Velociraptor is geologically younger than Deinonychus, but even more closely related. A specimen of Velociraptor has been found with quill knobs on the ulna. Quill knobs are where the follicular ligaments attached, and are a direct indicator of feathers of modern aspect.[25]

Classification

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Deinonychus antirrhopus is one of the best known dromaeosaurid species,[34] and also a close relative of the smaller Velociraptor, which is found in younger, Late Cretaceous-age rock formations in Central Asia.[35][36] The clade they form is called Velociraptorinae. The subfamily name Velociraptorinae was first coined by Rinchen Barsbold in 1983[37] and originally contained the single genus Velociraptor. Later, Phil Currie included most of the dromaeosaurids.[38] Two Late Cretaceous genera, Tsaagan from Mongolia[35] and the North American Saurornitholestes,[28] may also be close relatives, but the latter is poorly known and hard to classify.[35] Velociraptor and its allies are regarded as using their claws more than their skulls as killing tools, as opposed to dromaeosaurines like Dromaeosaurus, which have stockier skulls.[28] Phylogenetically, the dromaeosaurids represent one of the non-avialan dinosaur groups most closely related to birds.[39] The cladogram below follows a 2015 analysis by paleontologists Robert DePalma, David Burnham, Larry Martin, Peter Larson, and Robert Bakker, using updated data from the Theropod Working Group. This study currently classifies Deinonychus as a member of the Dromaeosaurinae.[40]

 
Size of Deinonychus (6) compared with other dromaeosaurids
Dromaeosauridae

A 2021 study of the dromaeosaurid Kansaignathus recovered Deinonychus as a velociraptorine rather than a dromaeosaurine, with Kansaignathus being an intermediate basal form more advanced than Deinonychus but more primitive than Velociraptor.[41][42] The cladogram below showcases these newly described relationships:

Dromaeosauridae

A study in 2022 however, reclassified Deinonychus as a basal member of Dromaeosaurinae again.[43]

Paleobiology

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Predatory behavior

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Interpretation of a Deinonychus preying on a Zephyrosaurus in manner suggested by Fowler et al. (2011)

In 2009, Manning and colleagues interpreted dromaeosaur claw tips as functioning as a puncture and gripping element, whereas the expanded rear portion of the claw transferred load stress through the structure.[44] They argue that the anatomy, form, and function of the foot's recurved digit II and hand claws of dromaeosaurs support a prey capture/grappling/climbing function. The team also suggest that a ratchet-like ‘‘locking’’ ligament might have provided an energy-efficient way for dromaeosaurs to hook their recurved digit II claw into prey. Shifting body weight locked the claws passively, allowing their jaws to dispatch prey. They conclude that the enhanced climbing abilities of dromaeosaur dinosaurs supported a scansorial (climbing) phase in the evolution of flight.[44]

 
 
Illustrations of various hypotheses for how dromaeosaurids used their sickle-claws (left, feathers omitted for clarity), and of the "Raptor Prey Restraint" model, a hypothesis supported by 21st century studies (right)

In 2011, Denver Fowler and colleagues suggested a new method by which Deinonychus and other dromaeosaurs may have captured and restrained prey.[45] This model, known as the "raptor prey restraint" (RPR) model of predation, proposes that Deinonychus killed its prey in a manner very similar to extant accipitrid birds of prey: by leaping onto its quarry, pinning it under its 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. However, the short metatarsus and foot strength would have been more similar to that of owls. The RPR method of predation would be consistent with other aspects of Deinonychus's anatomy, such as their unusual jaw and arm morphology. The arms were likely covered in long feathers, and may have been used as flapping stabilizers for balance while atop struggling prey, along with the stiff counterbalancing tail. Its jaws, thought to have had a comparatively weak bite force,[46] might be used for saw motion bites, like the modern Komodo dragon which also has a weak bite force, to finish off its prey if its kicks were not powerful enough.[47]

Bite force

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Reconstructed skull and neck, Royal Ontario Museum

Bite force estimates for Deinonychus were first produced in 2005, based on reconstructed jaw musculature. This study concluded that Deinonychus likely had a maximum bite force only 15% that of the modern American alligator.[46] A 2010 study by Paul Gignac and colleagues attempted to estimate the bite force based directly on newly discovered Deinonychus tooth puncture marks in the bones of a Tenontosaurus. These puncture marks came from a large individual, and provided the first evidence that large Deinonychus could bite through bone. Using the tooth marks, Gignac's team were able to determine that the bite force of Deinonychus was significantly higher than earlier studies had estimated by biomechanical studies alone. They found the bite force of Deinonychus to be between 4,100 and 8,200 newtons, greater than living carnivorous mammals including the hyena, and equivalent to a similarly-sized alligator.[48]

However, this estimate has come into question, as it was based on bite marks rather than a Deinonychus skull. A recent 2022 study used a Deinonychus skull for their estimate and calculated 706 Newtons.[49]

Gignac and colleagues also noted, however, that bone puncture marks from Deinonychus are relatively rare, and unlike larger theropods with many known puncture marks like Tyrannosaurus, Deinonychus probably did not frequently bite through or eat bone. Instead, they probably used their strong bite force for defense or to capture prey, rather than for feeding.[48]

A 2024 study by Tse, Miller, and Pittman et al., focusing on the skull morphology and bite forces of various dromaeosaurids discovered that Deinonychus, the largest taxon examined, had a skull that was well adapted to hunting of large vertebrates and delivering powerful bites to prey alongside Dromaeosaurus, to which it was compared. In this study, Deinonychus represented the most extreme specializations compared to other dromaeosaurids when it came to its adaptations. The same study also revealed that Deinonychus' skull was less resistant to bite forces than that of Velociraptor, which apparently was engaging in more scavenging behavior, suggesting high bite force resistance was more common in dromaeosaurid taxa that were obtaining food through scavenging more than engaging in active predation. It is also suggested in these findings that Deinonychus may have fed by using neck-driven pullback movements to dismember carcasses when feeding, akin to modern varanid lizards.[50]

Limb function

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Cast in climbing posture

Despite being the most distinctive feature of Deinonychus, the shape and curvature of the sickle claw varies between specimens. The type specimen described by Ostrom in 1969 has a strongly curved sickle claw, while a newer specimen described in 1976 had a claw with much weaker curvature, more similar in profile with the 'normal' claws on the remaining toes.[13] Ostrom suggested that this difference in the size and shape of the sickle claws could be due to individual, sexual, or age-related variation, but admitted he could not be sure.

There is anatomical[2] and trackway[51] evidence that this talon was held up off the ground while the dinosaur walked on the third and fourth toes.

Ostrom suggested that Deinonychus could kick with the sickle claw to cut and slash at its prey.[2] Some researchers even suggested that the talon was used to disembowel large ceratopsian dinosaurs.[52] Other studies have suggested that the sickle claws were not used to slash but rather to deliver small stabs to the victim.[53] In 2005, Manning and colleagues ran tests on a robotic replica that precisely matched the anatomy of Deinonychus and Velociraptor, and used hydraulic rams to make the robot strike a pig carcass. In these tests, the talons made only shallow punctures and could not cut or slash. The authors suggested that the talons would have been more effective in climbing than in dealing killing blows.[54] In 2009, Manning and colleagues undertook additional analysis dromaeosaur claw function, using a numerical modelling approach to generate a 3D finite element stress/ strain map of a Velociraptor hand claw.[44] They went on to quantitatively evaluate the mechanical behavior of dromaeosaur claws and their function. They state that dromaeosaur claws were well-adapted for climbing as they were resistant to forces acting in a single (longitudinal) plane, due to gravity.

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.[2] The cassowary has claws up to 125 mm (4.9 in) long.[55] Ostrom cited Gilliard (1958) in saying that they can sever an arm or disembowel a man.[56] 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.[57][58] Cassowaries use their claws to defend themselves, to attack threatening animals, and in agonistic displays such as the Bowed Threat Display.[55] The seriema also has an enlarged second toe claw, and uses it to tear apart small prey items for swallowing.[59] In 2011, a study suggested that the sickle claw would likely have been used to pin down prey while biting it, rather than as a slashing weapon.[45]

 
Hand bones of MOR 747

Biomechanical studies by Ken Carpenter in 2002 confirmed that the most likely function of the forelimbs in predation was grasping, as their great lengths would have permitted longer reach than for most other theropods. The rather large and elongated coracoid, indicating powerful muscles in the forelimbs, further strengthened this interpretation.[60] Carpenter's biomechanical studies using bone casts also showed that Deinonychus could not fold its arms against its body like a bird ("avian folding"), contrary to what was inferred from the earlier 1985 descriptions by Jacques Gauthier[61] and Gregory S. Paul in 1988.[28]

Studies by Phil Senter in 2006 indicated that Deinonychus forelimbs could be used not only for grasping, but also for clutching objects towards the chest. If Deinonychus had feathered fingers and wings, the feathers would have limited the range of motion of the forelimbs to some degree. For example, when Deinonychus extended its arm forward, the 'palm' of the hand automatically rotated to an upward-facing position. This would have caused one wing to block the other if both forelimbs were extended at the same time, leading Senter to conclude that clutching objects to the chest would have only been accomplished with one arm at a time. The function of the fingers would also have been limited by feathers; for example, only the third digit of the hand could have been employed in activities such as probing crevices for small prey items, and only in a position perpendicular to the main wing.[26] Alan Gishlick, in a 2001 study of Deinonychus forelimb mechanics, found that even if large wing feathers were present, the grasping ability of the hand would not have been significantly hindered; rather, grasping would have been accomplished perpendicular to the wing, and objects likely would have been held by both hands simultaneously in a "bear hug" fashion, findings which have been supported by the later forelimb studies by Carpenter and Senter.[62] In a 2001 study conducted by Bruce Rothschild and other paleontologists, 43 hand bones and 52 foot bones referred to Deinonychus were examined for signs of stress fracture; none were found.[63] The second phalanx of the second toe in the specimen YPM 5205 has a healed fracture.[64]

 
Foot (MOR 747) in flexion

Parsons and Parsons have shown that juvenile and sub-adult specimens of Deinonychus display some morphological differences from the adults. For instance, the arms of the younger specimens were proportionally longer than those of the adults, a possible indication of difference in behavior between young and adults.[65] Another example of this could be the function of the pedal claws. Parsons and Parsons have suggested that the claw curvature (which Ostrom [1976] had already shown was different between specimens[13]) maybe was greater for juvenile Deinonychus, as this could help it climb in trees, and that the claws became straighter as the animal became older and started to live solely on the ground.[66] This was based on the hypothesis that some small dromaeosaurids used their pedal claws for climbing.[54]

Locomotion

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Dromaeosaurids, especially Deinonychus, are often depicted as unusually fast-running animals in the popular media, and Ostrom himself speculated that Deinonychus was fleet-footed in his original description.[10] However, when first described, a complete leg of Deinonychus had not been found, and Ostrom's speculation about the length of the femur (upper leg bone) later proved to have been an overestimate. In a later study, Ostrom noted that the ratio of the femur to the tibia (lower leg bone) is not as important in determining speed as the relative length of the foot and lower leg. In modern fleet-footed birds, like the ostrich, the foot-tibia ratio is .95. In unusually fast-running dinosaurs, like Struthiomimus, the ratio is .68, but in Deinonychus the ratio is .48. Ostrom stated that the "only reasonable conclusion" is that Deinonychus, while far from slow-moving, was not particularly fast compared to other dinosaurs, and certainly not as fast as modern flightless birds.[13]

The low foot to lower leg ratio in Deinonychus is due partly to an unusually short metatarsus (upper foot bones). The ratio is actually larger in smaller individuals than in larger ones. Ostrom suggested that the short metatarsus may be related to the function of the sickle claw, and used the fact that it appears to get shorter as individuals aged as support for this. He interpreted all these features—the short second toe with enlarged claw, short metatarsus, etc.—as support for the use of the hind leg as an offensive weapon, where the sickle claw would strike downwards and backwards, and the leg pulled back and down at the same time, slashing and tearing at the prey. Ostrom suggested that the short metatarsus reduced overall stress on the leg bones during such an attack, and interpreted the unusual arrangement of muscle attachments in the Deinonychus leg as support for his idea that a different set of muscles was used in the predatory stroke than in walking or running. Therefore, Ostrom concluded that the legs of Deinonychus represented a balance between running adaptations needed for an agile predator, and stress-reducing features to compensate for its unique foot weapon.[13]

 
Restoration of a walking individual

In his 1981 study of Canadian dinosaur footprints, Richard Kool produced rough walking speed estimates based on several trackways made by different species in the Gething Formation of British Columbia. Kool estimated one of these trackways, representing the ichnospecies Irenichnites gracilis (which may have been made by Deinonychus), to have a walking speed of 10.1 kilometers per hour (6 miles per hour).[67]

In a 2015 paper, it was reported after further analysis of immature fossils that the open and mobile nature of the shoulder joint might have meant that young Deinonychus were capable of some form of flight.[68]

Eggs

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Artist's impression of an individual in brooding position

The identification, in 2000, of a probable Deinonychus egg associated with one of the original specimens allowed comparison with other theropod dinosaurs in terms of egg structure, nesting, and reproduction. In their 2006 examination of the specimen, Grellet-Tinner and Makovicky examined the possibility that the dromaeosaurid had been feeding on the egg, or that the egg fragments had been associated with the Deinonychus skeleton by coincidence. They dismissed the idea that the egg had been a meal for the theropod, noting that the fragments were sandwiched between the belly ribs and forelimb bones, making it impossible that they represented contents of the animal's stomach. In addition, the manner in which the egg had been crushed and fragmented indicated that it had been intact at the time of burial, and was broken by the fossilization process. The idea that the egg was randomly associated with the dinosaur was also found to be unlikely; the bones surrounding the egg had not been scattered or disarticulated, but remained fairly intact relative to their positions in life, indicating that the area around and including the egg was not disturbed during preservation. The fact that these bones were belly ribs (gastralia), which are very rarely found articulated, supported this interpretation. All the evidence, according to Grellet-Tinner and Makovicky, indicates that the egg was intact beneath the body of the Deinonychus when it was buried. It is possible that this represents brooding or nesting behavior in Deinonychus similar to that seen in the related troodontids and oviraptorids, or that the egg was in fact inside the oviduct when the animal died.[8]

Examination of the Deinonychus egg's microstructure confirms that it belonged to a theropod, since it shares characteristics with other known theropod eggs and shows dissimilarities with ornithischian and sauropod eggs. Compared to other maniraptoran theropods, the egg of Deinonychus is more similar to those of oviraptorids than to those of troodontids, despite studies that show the latter are more closely related to dromaeosaurids like Deinonychus. While the egg was too badly crushed to accurately determine its size, Grellet-Tinner and Makovicky estimated a diameter of about 7 cm (2.8 in) based on the width of the pelvic canal through which the egg had to have passed. This size is similar to the 7.2 cm (2.8 in) diameter of the largest Citipati (an oviraptorid) eggs; Citipati and Deinonychus also shared the same overall body size, supporting this estimate. Additionally, the thicknesses of Citipati and Deinonychus eggshells are almost identical, and since shell thickness correlates with egg volume, this further supports the idea that the eggs of these two animals were about the same size.[8]

A study published in November 2018 by Norell, Yang and Wiemann et al., indicates that Deinonychus laid blue eggs, likely to camouflage them as well as creating open nests. The study also indicates that Deinonychus and other dinosaurs that created open nests likely represent an origin of color in modern bird eggs as an adaptation both for recognition and camouflage against predators.[69][70][71]

Social behavior

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Whether or not Deinonychus could’ve practiced cooperative pack hunting is still a hot debate.

Deinonychus teeth found in association with fossils of the ornithopod dinosaur Tenontosaurus are quite common in the Cloverly Formation. Two quarries have been discovered that preserve fairly complete Deinonychus fossils near Tenontosaurus fossils. The first, the Yale quarry in the Cloverly of Montana, includes numerous teeth, four adult Deinonychus and one juvenile Deinonychus. The association of this number of Deinonychus skeletons in a single quarry suggests that Deinonychus may have fed on that animal, and perhaps hunted it. Ostrom and Maxwell have even used this information to speculate that Deinonychus might have lived and hunted in packs.[72] The second such quarry is from the Antlers Formation of Oklahoma. The site contains six partial skeletons of Tenontosaurus of various sizes, along with one partial skeleton and many teeth of Deinonychus. One tenontosaur humerus even bears what might be Deinonychus tooth marks. Brinkman et al. (1998) point out that Deinonychus had an adult mass of 70–100 kg (150–220 lb), whereas adult tenontosaurs were 1–4 metric tons. A solitary Deinonychus could not kill an adult tenontosaur, suggesting that pack hunting is possible.[4]

A 2007 study by Roach and Brinkman has called into question the cooperative pack hunting behavior of Deinonychus, based on what is known of modern carnivore hunting and the taphonomy of tenontosaur sites. Modern archosaurs (birds and crocodiles) and Komodo dragons typically display little cooperative hunting; instead, they are usually either solitary hunters, or are drawn to previously killed carcasses, where much conflict 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 will attack smaller Komodos that attempt to feed; if the smaller animal is killed, it is cannibalized. When this information is applied to the tenontosaur sites, it appears that what is found is consistent with Deinonychus having a Komodo or crocodile-like feeding strategy. Deinonychus skeletal remains found at these sites are from subadults, with missing parts consistent with having been eaten by other Deinonychus.[73]

On the other hand, a paper by Li et al. describes track sites with similar foot spacing and parallel trackways, implying gregarious packing behavior instead of uncoordinated feeding behavior.[74] Contrary to the claim crocodilians do not hunt cooperatively, they have actually been observed to hunt cooperatively,[75][76] meaning that the notion of infighting, competition for food and cannibalism ruling out cooperative feeding may actually be a false dichotomy.

In 2020, study of carbon isotopes in Deinonychus teeth suggests precociality in the genus. The isotopes found for different aged specimens indicate that adults and juveniles had different diets across the various age groups. The data suggests that Deinonychus had a more typical archosaurian set of life stages, with any parental feeding of young ending before the young were large enough to share the typical adult diet. The examinations also have been stated to indicate a lack of mammal-like pack hunting. Despite this, the authors stated that this doesn’t exclude the possibility of gregarious and probably practiced ratite-like parental care, instead of a complete agnostic relationship as seen in Komodo dragons, due to the lack of spatial separation of juveniles and adults.[77]

Paleoenvironment

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Mounted skeletons of Deinonychus and the contemporary Zephyrosaurus (left), Natural History Museum of Denmark

Geological evidence suggests that Deinonychus inhabited a floodplain or swamplike habitat.[34] The paleoenvironment of both the upper Cloverly Formation and the Antlers Formation, in which remains of Deinonychus have been found, consisted of tropical or sub-tropical forests, deltas and lagoons, perhaps similar to the environment of modern-day Louisiana.[78][79] Other animals Deinonychus shared its world with include herbivorous dinosaurs such as the nodosaurid Sauropelta and the ornithopods Zephyrosaurus and Tenontosaurus. In Oklahoma, the ecosystem of Deinonychus also included the large theropod Acrocanthosaurus, the huge sauropod Sauroposeidon, the crocodilians Goniopholis and Paluxysuchus, and the gar Lepisosteus.[79] If the teeth found in Maryland are those of Deinonychus, then its contemporaries would include the sauropod Astrodon and the poorly-known nodosaur Priconodon. The middle portion of the Cloverly Formation ranges in age from 115 ± 10 Ma near the base[5] to 108.5 ± 0.2 Ma near the top.[6]

Cultural significance

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Feathered model adjacent to an earlier, featherless model from the Westphalian Museum of Natural History

Deinonychus were featured prominently in Harry Adam Knight's novel Carnosaur and its film adaption, and Michael Crichton's novels Jurassic Park and The Lost World and their film adaptations, directed by Steven Spielberg. Crichton ultimately chose to use the name Velociraptor for these dinosaurs, rather than Deinonychus. Crichton had met with John Ostrom several times during the writing process to discuss details of the possible range of behaviors and life appearance of Deinonychus. Crichton at one point apologetically told Ostrom that he had decided to use the name Velociraptor in place of Deinonychus for his book, because he felt the former name was "more dramatic". Despite this, according to Ostrom, Crichton stated that the Velociraptor of the novel was based on Deinonychus in almost every detail, and that only the name had been changed.[80]

The Jurassic Park filmmakers followed suit, designing the film's models based almost entirely on Deinonychus instead of the actual Velociraptor, and they reportedly requested all of Ostrom's published papers on Deinonychus during production.[80] As a result, they portrayed the film's dinosaurs with the size, proportions, and snout shape of Deinonychus.[2] The 20-foot-long (6.1 m) Utahraptor is commonly considered to be a close match to the film's dinosaurs, which are much larger than either Deinonychus or Velociraptor were in life.[81][82]

See also

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References

edit
  1. ^ "deinonychus". Dictionary.com Unabridged (Online). n.d.
  2. ^ a b c d e f g Ostrom, John Harold (1970). "Stratigraphy and paleontology of the Cloverly Formation (Lower Cretaceous) of the Bighorn Basin area, Wyoming and Montana". Bulletin of the Peabody Museum of Natural History. 35: 1–234.
  3. ^ 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.
  4. ^ a b Brinkman, D. L.; Cifelli, R. L.; Czaplewski, N. J. (1998). "First occurrence of Deinonychus antirrhopus (Dinosauria: Theropoda) from the Antlers Formation (Lower Cretaceous: Aptian–Albian) of Oklahoma". Oklahoma Geological Survey Bulletin. 146: 1–27.
  5. ^ a b Chen, Z.-Q.; Lubin, S. (1997). "A fission track study of the terrigenous sedimentary sequences of the Morrison and Cloverly Formations in northeastern Bighorn Basin, Wyoming". The Mountain Geologist. 34: 51–62.
  6. ^ a b Burton, D.; Greenhalgh, B.W.; Britt, B.B.; Kowallis, B.J.; Elliott, W.S.; Barrick, R. (2006). "New radiometric ages from the Cedar Mountain Formation, Utah and the Cloverly Formation, Wyoming: implications for contained dinosaur faunas". Geological Society of America Abstracts with Programs. 38 (7): 52.
  7. ^ Lipka, T. R. (1998). "The Affinities of the Enigmatic Theropods of the Arundel Clay Facies (Aptian), Potomac Formation, Atlantic Coastal Plain of Maryland". In Lucas, S.G.; Kirkland, J.I.; Estep, J.W. (eds.). Lower and Middle Cretaceous Terrestrial Ecosystems. New Mexico Museum of Natural History and Science Bulletin, 14. Albuquerque: New Mexico Museum of Natural History and Science. pp. 229–234. OCLC 40283894.
  8. ^ a b c d Grellet-Tinner, G.; Makovicky, P. (2006). "A possible egg of the dromaeosaur Deinonychus antirrhopus: phylogenetic and biological implications". Canadian Journal of Earth Sciences. 43 (6): 705–719. Bibcode:2006CaJES..43..705G. doi:10.1139/E06-033.
  9. ^ a b Norell, M. A.; Gaffney, E. S.; Dingus, L. (1995). Discovering Dinosaurs in the American Museum of Natural History. New York: Knopf. pp. 126–130. ISBN 978-0-679-43386-6.
  10. ^ a b c d e f 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.
  11. ^ Ostrom, John Harold (1969). "A new theropod dinosaur from the Lower Cretaceous of Montana". Postilla. 128: 1–17.
  12. ^ Ostrom, John H. (1974). "The Pectoral Girdle and Forelimb Function of Deinonychus (Reptilia: Saurischia) : A Correction". Postilla, Peabody Museum of Natural History Bulletin. 165: 1–11.
  13. ^ a b c d e Ostrom, J.H. (1976). "On a new specimen of the Lower Cretaceous theropod dinosaur Deinonychus antirrhopus". Breviora. 439: 1–21.
  14. ^ American Museum of Natural History (2007). "Deinonychus". American Museum of Natural History. Archived from the original on August 12, 2007. Retrieved July 13, 2007.
  15. ^ Parsons, W.L. & K.M. (2009). "Further Descriptions of the Osteology of Deinonychus antirrhopus (Saurischia, Theropoda)". Bulletin of the Buffalo Society of Natural Sciences. 38.
  16. ^ Makovicky, P.J.; Grellet-Tinner, G. (2000). "Association between a specimen of Deinonychus antirrhopus and theropod eggshell". In Bravo, A.M.; T. Reyes (eds.). First international symposium on dinosaur eggs and babies, Isona i Conca Dellà Catalonia, Spain, 23–26 September 1999. pp. 123–128.
  17. ^ Grellet-Tinner, Gerard (2006). "Oology And The Evolution Of Thermophysiology In Saurischian Dinosaurs: Homeotherm And Endotherm Deinonychosaurians?". Papéis Avulsos de Zoologia. 46 (1): 1–10. doi:10.1590/S0031-10492006000100001.
  18. ^ Erickson, Gregory M.; Curry Rogers, Kristina; Varricchio, David J.; Norell, Mark A.; Xu, Xing (2007). "Growth patterns in brooding dinosaurs reveals the timing of sexual maturity in non-avian dinosaurs and genesis of the avian condition". Biology Letters. 3 (5): 558–61. doi:10.1098/rsbl.2007.0254. PMC 2396186. PMID 17638674.
  19. ^ Fastovsky, D.E.; Weishampel, D.B. (2005). "Theropoda I: Nature Red in Tooth and Claw". In Fastovsky, D.E.; Weishampel, D.B. (eds.). The Evolution and Extinction of the Dinosaurs (2nd ed.). Cambridge: Cambridge University Press. pp. 265–299. ISBN 978-0-521-81172-9.
  20. ^ Ostrom, J. H. (1976). "Archaeopteryx and the origin of birds" (PDF). Biological Journal of the Linnean Society. 8 (2): 91–182. doi:10.1111/j.1095-8312.1976.tb00244.x.
  21. ^ Bakker, R.T. (1986). The Dinosaur Heresies. Kensington Publishing. p. 310. ISBN 978-0-8065-2260-9.
  22. ^ Long, J.A.; Schouten, P. (2008). "Deinonychus". Feathered Dinosaurs: The Origin of Birds. Oxford University Press. pp. 142–143. ISBN 978-0-19-537266-3.
  23. ^ Dixon, Dougal (2007). "Fast Hunters". The Illustrated Encyclopedia of Dinosaurs. Lorenz Books. pp. 160–161. ISBN 978-0-7548-1573-0.
  24. ^ a b c Xu, X.; Zhou, Z.; Wang, X.; Kuang, X.; Zhang, F. & Du, X. (2003). "Four-winged dinosaurs from China" (PDF). Nature. 421 (6921): 335–340. Bibcode:2003Natur.421..335X. doi:10.1038/nature01342. PMID 12540892. S2CID 1160118.
  25. ^ a b Turner, Alan H.; Makovicky, Peter J.; Norell, Mark A. (2007). "Feather quill knobs in the dinosaur Velociraptor". Science. 317 (5845): 1721. Bibcode:2007Sci...317.1721T. doi:10.1126/science.1145076. PMID 17885130. S2CID 11610649.
  26. ^ a b Senter, Phil (2006). "Comparison of Forelimb Function Between Deinonychus And Bambiraptor (Theropoda: Dromaeosauridae)". Journal of Vertebrate Paleontology. 26 (4): 897–906. doi:10.1671/0272-4634(2006)26[897:COFFBD]2.0.CO;2. S2CID 85919882.
  27. ^ Parsons, William L.; Parsons, Kristen M. (2009). "Further descriptions of the osteology of Deinonychus antirrhopus (Saurischia, Theropoda)". Bulletin of the Buffalo Society of Natural Sciences. 38.
  28. ^ a b c d Paul, Gregory Scott (1988). Predatory Dinosaurs of the World. New York: Simon and Schuster. pp. 358, 366–369. ISBN 978-0-671-61946-6.
  29. ^ Paul, G. S. (2016). The Princeton Field Guide to Dinosaurs (2nd ed.). Princeton, New Jersey: Princeton University Press. p. 153. ISBN 9780691167664.
  30. ^ Campione, Nicolas E.; Evans, David C.; Brown, Caleb M.; Carrano, Matthew T. (2014). "Body mass estimation in non-avian bipeds using a theoretical conversion to quadruped stylopodial proportions". Methods in Ecology and Evolution. 5 (9): 913–923. Bibcode:2014MEcEv...5..913C. doi:10.1111/2041-210X.12226. S2CID 84317234.
  31. ^ a b Maxwell, W. D. & Witmer, L. M. (1996). "New Material of Deinonychus (Dinosauria, Theropoda)". Journal of Vertebrate Paleontology. 16 (3): 51A. doi:10.1080/02724634.1996.10011371.
  32. ^ Witmer, Lawrence M. & Maxwell, William D. (1996). "The skull of Deinonychus (Dinosauria:Theropoda): New insights and implications". Journal of Vertebrate Paleontology. 16 (3): 73A. doi:10.1080/02724634.1996.10011371.
  33. ^ Hwang, S. H.; Norell, M. A.; Ji, Q. & Gao, K. (2002). "New Specimens of Microraptor zhaoianus (Theropoda: Dromaeosauridae) from Northeastern China" (PDF). American Museum Novitates (3381): 1–44. doi:10.1206/0003-0082(2002)381<0001:nsomzt>2.0.co;2. hdl:2246/2870. S2CID 54995804. Archived from the original (PDF) on January 2, 2014. Retrieved September 1, 2013.
  34. ^ a b Norell, M.A.; Makovicky, P.J. (2004). "Dromaeosauridae". In Weishampel, D.B.; Dodson, P.; Osmólska, H. (eds.). The Dinosauria (2nd ed.). Berkeley: University of California Press. pp. 196–210. ISBN 978-0-520-24209-8.
  35. ^ a b c Norell, M.A.; Clark, J.M.; Turner, A.H.; Makovicky, P.J.; Barsbold, R.; Rowe, T. (2006). "A new dromaeosaurid theropod from Ukhaa Tolgod (Ömnögov, Mongolia)" (PDF). American Museum Novitates (3545): 1–51. doi:10.1206/0003-0082(2006)3545[1:ANDTFU]2.0.CO;2. hdl:2246/5823. Archived from the original (PDF) on June 12, 2007. Retrieved July 7, 2007.
  36. ^ Turner, A.S.; Hwang, S.H.; 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. hdl:2246/5845. S2CID 31096081. Archived from the original (PDF) on March 26, 2009. Retrieved April 30, 2007.
  37. ^ Barsbold, R. (1983). "Carnivorous Dinosaurs from the Cretaceous of Mongolia". The Joint Soviet–Mongolian Palaeontological Expedition, Transactions. 19: 1–117.
  38. ^ Currie, P.J. (1995). "New information on the anatomy and relationships of Dromaeosaurus albertensis (Dinosauria: Theropoda)". Journal of Vertebrate Paleontology. 15 (3): 576–591. Bibcode:1995JVPal..15..576C. doi:10.1080/02724634.1995.10011250. (abstract Archived September 27, 2007, at the Wayback Machine)
  39. ^ Benton, M.J. (2004). Vertebrate Palaeontology (Third ed.). Blackwell Publishing. p. 472. ISBN 978-0-632-05637-8. Archived from the original on October 19, 2008. Retrieved July 8, 2007.
  40. ^ DePalma, Robert A.; Burnham, David A.; Martin, Larry D.; Larson, Peter L.; Bakker, Robert T. (2015). "The First Giant Raptor (Theropoda: Dromaeosauridae) from the Hell Creek Formation". Paleontological Contributions (14): 1–16. doi:10.17161/paleo.1808.18764. hdl:1808/18764.
  41. ^ Averianov, A. O.; Lopatin, A. V. (July 1, 2021). "A New Theropod Dinosaur (Theropoda, Dromaeosauridae) from the Late Cretaceous of Tajikistan". Doklady Earth Sciences. 499 (1): 570–574. Bibcode:2021DokES.499..570A. doi:10.1134/S1028334X21070047. S2CID 236478552 – via Springer Link.
  42. ^ Averianov, A. O.; Lopatin, A. V. (2021). "Новый хищный динозавр (Theropoda, Dromaeosauridae) из позднего мела Таджикистана" [A new theropod dinosaur (Theropoda, Dromaeosauridae) from the Late Cretaceous of Tajikistan]. Reports of the Russian Academy of Sciences. Earth Sciences (in Russian). 499 (1): 49–53. doi:10.31857/S2686739721070045. S2CID 239088573..
  43. ^ Powers, Mark J.; Fabbri, Matteo; Doschak, Michael R.; Bhullar, Bhart-Anjan S.; Evans, David C.; Norell, Mark A.; Currie, Philip J. (2022). "A new hypothesis of eudromaeosaurian evolution: CT scans assist in testing and constructing morphological characters". Journal of Vertebrate Paleontology. 41 (5): e2010087. Bibcode:2021JVPal..41E0087P. doi:10.1080/02724634.2021.2010087. S2CID 247039404.
  44. ^ a b c Manning, P. L., Margetts, L., Johnson, M. R., Withers, P., Sellers, W. I., Falkingham, P. L., Mummery, P. M., Barrett, P. M. and Raymont, D. R. 2009. Biomechanics of dromaeosaurid dinosaur claws: application of x-ray microtomography, nanoindentation and finite element analysis. Anatomical Record, 292, 1397-1405.
  45. ^ a b Fowler, D. W.; Freedman, E. A.; Scannella, J. B.; Kambic, R. E. (2011). Farke, Andrew Allen (ed.). "The Predatory Ecology of Deinonychus and the Origin of Flapping in Birds". PLOS ONE. 6 (12): e28964. Bibcode:2011PLoSO...628964F. doi:10.1371/journal.pone.0028964. PMC 3237572. PMID 22194962.
  46. ^ a b Therrien, F.; Henderson, D.M.; Huff, C.B. (2005). "Bite me: biomechanical models of theropod mandibles and implications for feeding behavior". In Carpenter, Kenneth (ed.). The Carnivorous Dinosaurs. Indianapolis: Indiana University Press. pp. 179–237. ISBN 978-0-253-34539-4.
  47. ^ Sakamoto, M. (2010). "Jaw biomechanics and the evolution of biting performance in theropod dinosaurs". Proceedings of the Royal Society B: Biological Sciences. 277 (1698): 3327–3333. doi:10.1098/rspb.2010.0794. PMC 2981932. PMID 20534620.
  48. ^ a b Gignac, P.M.; Makovicky, P.J.; Erickson, G.M.; Walsh, R.P. (2010). "A description of Deinonychus antirrhopus bite marks and estimates of bite force using tooth indentation simulations". Journal of Vertebrate Paleontology. 30 (4): 1169–1177. Bibcode:2010JVPal..30.1169G. doi:10.1080/02724634.2010.483535. S2CID 86182457.
  49. ^ "Estimating bite force in extinct dinosaurs using phylogenetically predicted physiological cross-sectional areas of jaw adductor muscles" (PDF).
  50. ^ Tse, Yuen Ting; Miller, Case Vincent; Pittman, Michael (2024). "Morphological disparity and structural performance of the dromaeosaurid skull informs ecology and evolutionary history". BMC Ecology and Evolution. 24 (1): 39. Bibcode:2024BMCEE..24...39T. doi:10.1186/s12862-024-02222-5. PMC 11020771. PMID 38622512.
  51. ^ Li, Rihui; Lockley, Martin G.; Makovicky, Peter J.; Matsukawa, Masaki; Norell, Mark A.; Harris, Jerald D.; Liu, Mingwei (2007). "Behavioral and faunal implications of deinonychosaur trackways from China". Naturwissenschaften. 95 (3): 185–91. Bibcode:2008NW.....95..185L. doi:10.1007/s00114-007-0310-7. PMID 17952398. S2CID 16380823.
  52. ^ Adams, Dawn (1987) "The bigger they are, the harder they fall: Implications of ischial curvature in ceratopsian dinosaurs" pp. 1–6 in Currie, Philip J. and Koster, E. (eds) Fourth symposium on mesozoic terrestrial ecosystems. Tyrrell Museum, Drumheller, Canada
  53. ^ Carpenter, Kenneth (1998). "Evidence of predatory behavior by carnivorous dinosaurs". Gaia. 15: 135–144.
  54. ^ a b Manning, Phil L.; Payne, David; Pennicott, John; Barrett, Paul M.; Ennos, Roland A. (2006). "Dinosaur killer claws or climbing crampons?". Biology Letters. 2 (1): 110–112. doi:10.1098/rsbl.2005.0395. PMC 1617199. PMID 17148340.
  55. ^ a b Davies, S. J. J. F. (2002). Ratites and Tinamous. New York: Oxford University Press. ISBN 978-0-19-854996-3.
  56. ^ Gilliard, E. T. (1958). Living birds of the world. Garden City, NY: Doubleday.
  57. ^ Kofron, Christopher P. (1999) "Attacks to humans and domestic animals by the southern cassowary (Casuarius casuarius johnsonii) in Queensland, Australia
  58. ^ Kofron, Christopher P. (2003). "Case histories of attacks by the southern cassowary in Queensland". Memoirs of the Queensland Museum. 49 (1): 335–338.
  59. ^ Redford, Kent H.; Peters, Gustav. "Notes on the biology and song of the red-legged seriema (cariama cristata)". Journal of Field Ornithology. 57 (4): 261–269.
  60. ^ Carpenter, Kenneth (2002). "Forelimb biomechanics of nonavian theropod dinosaurs in predation". Senckenbergiana Lethaea. 82: 59–76. doi:10.1007/BF03043773. S2CID 84702973.
  61. ^ Gauthier, J.; Padian, K. (1985). M.K. Hecht; J.H. Ostrom; G. Viohl; P. Wellnhofer (eds.). Phylogenetic, Functional, And Aerodynamic Analyses Of The Origin Of Birds And Their Flight. The Beginnings Of Birds. Proceedings of the International Archaeopteryx Conference, Eichstätt, 1984. Eischtatt: Freunde des Jura-Museums Eichstätt. pp. 185–197. ISBN 3-9801178-0-4.
  62. ^ Gishlick, A.D. (2001). "The function of the manus and forelimb of Deinonychus antirrhopus and its importance for the origin of avian flight". In Gauthier, J.; Gall, L.F. (eds.). New Perspectives on the Origin and Early Evolution of Birds. New Haven: Yale Peabody Museum. pp. 301–318.
  63. ^ 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, pp. 331–336.
  64. ^ Molnar, R. E., 2001, Theropod paleopathology: a literature survey: In: Mesozoic Vertebrate Life, edited by Tanke, D. H., and Carpenter, K., Indiana University Press, pp. 337–363.
  65. ^ Parsons, W.; Parsons, K. (2006). "Morphology and size of an adult specimen of Deinonychus antirrhopus, (Saurischia, Theropoda)". Journal of Vertebrate Paleontology. 26 (3 sup): 109A. doi:10.1080/02724634.2006.10010069. S2CID 220413406.
  66. ^ Parsons, W. L.; Parsons, K. M. (2009). "Further descriptions of the osteology of Deinonychus antirrhopus (Saurischia, Theropoda)" (PDF). Bulletin of the Buffalo Society of Natural Sciences. 38: 43–54. Archived from the original (PDF) on July 3, 2010. Retrieved November 14, 2010.
  67. ^ Kool, R. (1981). "The walking speed of dinosaurs from the Peace River Canyon, British Columbia, Canada". Canadian Journal of Earth Sciences. 18 (4): 823–825. Bibcode:1981CaJES..18..823K. doi:10.1139/e81-077.
  68. ^ Parsons, W. L.; Parsons, K. M. (2015). "Morphological Variations within the Ontogeny of Deinonychus antirrhopus (Theropoda, Dromaeosauridae)". PLOS ONE. 10 (4): e0121476. Bibcode:2015PLoSO..1021476P. doi:10.1371/journal.pone.0121476. PMC 4398413. PMID 25875499. e0121476.
  69. ^ Wiemann, Jasmina; Yang, Tzu-Ruei; Norell, Mark A. (2018). "Dinosaur egg colour had a single evolutionary origin". Nature. 563 (7732): 555–558. Bibcode:2018Natur.563..555W. doi:10.1038/s41586-018-0646-5. PMID 30464264. S2CID 53188171.
  70. ^ "Dinosaur Egg Color Had a Single Evolutionary Origin". November 2018.
  71. ^ "Dinosaurs put all colored bird eggs in one basket, evolutionarily speaking". October 31, 2018.
  72. ^ Maxwell, W. D.; Ostrom, J.H. (1995). "Taphonomy and paleobiological implications of Tenontosaurus–Deinonychus associations". Journal of Vertebrate Paleontology. 15 (4): 707–712. Bibcode:1995JVPal..15..707M. doi:10.1080/02724634.1995.10011256. (abstract Archived September 27, 2007, at the Wayback Machine)
  73. ^ 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. S2CID 84175628.
  74. ^ Li, Rihui; Lockley, Martin G.; Makovicky, Peter J.; Matsukawa, Masaki; Norell, Mark A.; Harris, Jerald D.; Liu, Mingwei (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. S2CID 16380823.
  75. ^ Lang, J. W. (2002). "Crocodilians". In Halliday, T.; Adler, K. (eds.). The Firefly Encyclopedia of Reptiles and Amphibians. Firefly Books. pp. 212–221. ISBN 978-1-55297-613-5.
  76. ^ Dinets, Vladimir (2015). "Apparent coordination and collaboration in cooperatively hunting crocodilians". Ethology Ecology & Evolution. 27 (2): 244–250. Bibcode:2015EtEcE..27..244D. doi:10.1080/03949370.2014.915432. S2CID 84672219.
  77. ^ Frederickson, J. A.; Engel, M. H.; Cifelli, R. L. (August 15, 2020). "Ontogenetic dietary shifts in Deinonychus antirrhopus (Theropoda; Dromaeosauridae): Insights into the ecology and social behavior of raptorial dinosaurs through stable isotope analysis". Palaeogeography, Palaeoclimatology, Palaeoecology. 552: 4–7. Bibcode:2020PPP...55209780F. doi:10.1016/j.palaeo.2020.109780. S2CID 219059665.
  78. ^ Forster, C. A. (1984). "The paleoecology of the ornithopod dinosaur Tenontosaurus tilletti from the Cloverly Formation, Big Horn Basin of Wyoming and Montana". The Mosasaur. 2: 151–163.
  79. ^ a b Wedel, M. J.; Cifelli, R. L. (2005). "Sauroposeidon: Oklahoma's Native Giant" (PDF). Oklahoma Geology Notes. 65 (2): 40–57. Archived from the original (PDF) on July 5, 2008.
  80. ^ a b Cummings, M. "Yale's legacy in Jurassic World." Yale News, June 18, 2015.
  81. ^ Vanhooker, Brian (September 16, 2021). "Spielberg's raptor: The wild, true story behind "Utahraptor spielbergi"". Inverse. Retrieved August 26, 2023.
  82. ^ Black, Riley (February 22, 2011). "What Do We Really Know About Utahraptor? | Dinosaur Tracking". Smithsonian Magazine. doi:10.1080/02724634.2001.10010852. S2CID 220414868. Retrieved January 24, 2013.
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