Ornitholestes Scale

''Ornitholestes'' (meaning "bird robber") is a small theropod dinosaur of the late Jurassic ( Brushy Basin Member of the Morrison Formation, middle Kimmeridgian age, about 154 million years agoTurner, C.E. and Peterson, F., (1999). "Biostratigraphy of dinosaurs in the Upper Jurassic Morrison Formation of the Western Interior, U.S.A." Pp. 77–114 in Gillette, D.D. (ed.), ''Vertebrate Paleontology in Utah''. Utah Geological Survey Miscellaneous Publication 99-1.) of Western Laurasia (the area that was to become North America).

To date, ''Ornitholestes'' is known only from a single partial skeleton with a badly crushed skull found at the Bone Cabin Quarry near Medicine Bow, Wyoming, in 1900. It was described by Henry Fairfield Osborn in 1903. An incomplete hand was later attributed to ''Ornitholestes'', although it now appears to belong to ''Tanycolagreus''. The type (and only known) species is ''O. hermanni''. The specific name honors the American Museum of Natural History preparator Adam Hermann.

Discovery and naming

''Ornitholestes'' was the first theropod to be discovered in the 1900s. The holotype skeleton (AMNH 619) was excavated in July 1900 in the Bone Cabin Quarry in Wyoming by an American Museum of Natural History expedition by Peter C. Kaisen, Paul Miller and Frederic Brewster Loomis. It represents a partial skeleton with skull, including numerous elements of the vertebral column, the forelimbs, pelvis and hindlimbs. Henry Fairfield Osborn named and scientifically described the specimen in 1903. The genus name ''Ornitholestes'', initially suggested by Theodore Gill, means "bird robber" and is derived from the Greek ''ὄρνις''/''ornis'', ''ornithos'' ("bird") and ''λῃστήσ''/''lestes'' ("robber"). The species name (''O. hermanni'') honors Adam Hermann, the head preparator at the Museum, who directed the restoration and mounting of the skeleton.

An incomplete hand (AMNH 587) was assigned to ''Ornitholestes'' by Osborn in his 1903 description of the genus. However, as Gregory S. Paul (1988) noted, the poor preservation of the corresponding elements in the type specimen made this association "tentative." In 2005, Kenneth Carpenter ''et al''. described a new small theropod, ''Tanycolagreus'', whose skeleton was found in Bone Cabin Quarry only a few hundred yards from AMNH 587. Since AMNH 587 was virtually identical to the preserved hand of the ''Tanycolagreus'' type specimen, it is now considered to belong to that dinosaur and not to ''Ornitholestes''. Following this reassignment, Phil Senter (2006) noted that "our knowledge of ''Ornitholestes'' can be drawn now only from the holotype." John Foster (2007) reported that some fragments from Dry Mesa Quarry may belong to ''Ornitholestes'', though these have not yet been described.

In 1920 Charles Whitney Gilmore concluded that ''Ornitholestes'' was identical to '' Coelurus''; in 1934 Oliver Perry Hay recognised only a difference at the species level, naming a ''Coelurus hermanni'', but in 1980 John Ostrom revived the genus.

Description

In his 1903 description, Osborn wrote that the length of ''Ornitholestes'' along "the skull and vertebral column as restored" was .Osborn (1903), p. 459 However, this reconstruction was inaccurate, being based in part on Othniel Charles Marsh's restoration of the basal sauropodomorph '' Anchisaurus'', and the neck and trunk were both too elongated. David Norman (1985) and John Foster (2007) both estimated that ''Ornitholestes'' was about long. Gregory S. Paul's 1988 ''Predatory Dinosaurs of the World'' listed the length of ''Ornitholestes'' as approximately . Paul (1988) and Foster (2007) both estimated that ''Ornitholestes'' weighed . John A. Long and Peter Schouten (2008) suggested a slightly higher figure, .

''Ornitholestes'' was a bipedal carnivore. Its head was proportionally smaller than that of most other predatory dinosaurs, but the skull was heavily built, with a short snout and robust lower jaw. The orbits (eye sockets) were quite large, measuring over 25 percent of the skull's length. There is no indication of a bony eye ring.Paul (1988b), p. 6

The front teeth of ''Ornitholestes'' were somewhat conical, with reduced serrations; the back teeth were recurved and more sharply serrated, similar to those of other theropod dinosaurs. Henry Fairfield Osborn (1903) counted four teeth in the premaxilla, of which the front tooth was the largest in the upper jaw. In contrast, Gregory S. Paul (1988) depicted the skull with only three premaxillary teeth remaining, much smaller than those illustrated by Osborn. Each maxilla (main tooth-bearing bone in the upper jaw) contained ten teeth, and each dentary (tooth-bearing bone in the lower jaw) contained twelve teeth. The tooth rows of ''Ornitholestes'' were short, with the dentary (lower) row being even shorter than the maxillary (upper) row, even though the dentary bone itself was exceptionally long at the back, reaching a point below the middle of the eye socket. Teeth did not extend as far back as the orbits, and neither tooth row spanned much more than one-third of the skull.

An area of broken bone near the external naris (nostril) appears to bulge upward, which led Gregory S. Paul to suggest in ''Predatory Dinosaurs of the World'' (1988) that ''Ornitholestes'' had a nasal horn "rather like a chicken's comb in looks."Paul (1988a), p. 303 Both Oliver W.M. Rauhut (2003) and Kenneth Carpenter ''et al''. (2005a) rejected that interpretation, and indicated that the upward flare of bone was due to post-mortem crushing of the skull. Paul's updated illustration of ''Ornitholestes'' in his 2010 ''Princeton Field Guide to Dinosaurs'' no longer contains the nasal horn.

''Ornitholestes'' had a relatively short neck with a slight sigmoidal (S-shaped) curve. The tail was long and whiplike, comprising over half of the body's length. Not all of the vertebrae were preserved, but Osborn (1917) estimated that ''Ornitholestes'' had nine or ten cervical (neck) vertebrae, thirteen dorsal (back) vertebrae, four sacral (hip) vertebrae, and 39 to 44 caudal (tail) vertebrae. Carpenter ''et al''. (2005a) recorded that the specimen contained five sacral vertebrae. ''Ornitholestes'' was a short-bodied theropod, and this was reflected in the short front-to-back dimensions of the cervical and dorsal vertebrae.

The forelimbs of ''Ornitholestes'' were relatively long, slightly under two-thirds the length of the hind legs. The humerus (upper arm bone) was heavily built, and somewhat longer than the radius and ulna (forearm bones). Both the humerus and radius were straight-shafted. The claws on digits I and II of the hand were about the same size.Senter (2006), p. 1030 Although the hand's third ungual (claw bone) was not preserved, extrapolation from the closest relatives of ''Ornitholestes'' indicates that it was probably shorter than the first two.

''Ornitholestes'' is often portrayed as a fast, long-legged theropod, but its lower limb bones were fairly short. Osborn (1917) calculated that the, missing, tibia (shin bone) was only about 70.6% as long as the femur (thigh bone). The metatarsals (foot bones) were spaced closely, but not fused together. As is typical of theropods, the feet were tridactyl (with three clawed weight-bearing toes). John H. Ostrom (1969) noted that the claw of digit II (the innermost toe) was larger than those of digits III and IV, and suggested that this digit may have borne a modified sickle claw similar to that of '' Deinonychus''. However, as both Ostrom (1969) and Paul (1988) noted, the poor preservation of digit II makes this hypothesis difficult to confirm.

Classification

The infraorder Coelurosauria, coined in 1914 by Friedrich von Huene, was traditionally a taxonomic wastebasket into which all small theropods were placed. ''Ornitholestes'', due to its small size, was therefore generally classified as a coelurosaur.Glut (1997), p. 645 In 1986, Jacques Gauthier redefined this and several other paleontological terms in a more rigorous fashion, based on cladistic methods. Tetanurae was defined as modern birds and all theropods more closely related to modern birds than to ceratosaurs, while Coelurosauria now comprised all members of Tetanurae more closely related to modern birds than to carnosaurs. In 1988, Gregory S. Paul suggested that ''Ornitholestes'' was very similar in skull structure to '' Proceratosaurus'', a Middle Jurassic theropod from England. He placed these two genera together in Ornitholestinae—a new subfamily under Allosauridae—and speculated that they were more closely related to the much larger '' Allosaurus'' than to other small theropods. However, the classification of ''Ornitholestes'' and ''Proceratosaurus'' as allosaur relatives proved untenable (the latter has since proved to be a tyrannosauroid), and Paul eventually abandoned it. All published cladistic analyses have shown ''Ornitholestes'' to be a coelurosaur as defined by Gauthier. Some analysis have shown support for the hypothesis that it is the most primitive member of the group Maniraptora, though more thorough analyses have suggested it is more primitive than the Maniraptoriformes, and possibly a close relative of the "compsognathid" '' Juravenator starkii''.

The following family tree illustrates a synthesis of the relationships of the major coelurosaurian groups based on various studies conducted in the 2010s.Hendrickx, C., Hartman, S.A., & Mateus, O. (2015). An Overview of Non- Avian Theropod Discoveries and Classification. ''PalArch’s Journal of Vertebrate Palaeontology'', 12(1): 1-73.

Paleobiology

In a 2001 study conducted by Bruce Rothschild and other paleontologists, 20 foot bones referred to ''Ornitholestes'' were examined for signs of stress fracture, but none were found.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.

Forelimb function

A biomechanical study conducted by Phil Senter (2006) used articulated casts of the ''Ornitholestes'' type specimen's right forelimb to determine its range of motion. Senter found that the antebrachium (forearm) could swing freely within a 95 ° range.Senter (2006), p. 1030–1031 When flexed (bent inward) at the elbow joint to the maximum possible extent, the humerus (upper arm bone) and radius (a lower arm bone) formed a 53° angle. The ability of ''Ornitholestes'' to bend the forearm to an angle significantly more acute than 90° is characteristic of Maniraptoriformes, but absent in more primitive theropods such as '' Coelophysis'' and ''Allosaurus''.

Even when fully extended (straightened) at the elbow, the forearm did not form a straight angle, falling short of this by 22°. Pronation (twisting to make the palmar side of the hand face downwards) of the forearm was impossible, because the radius and ulna lacked rolling surfaces, meaning the forearm was in a permanent state of supination.

When ''Ornitholestes'' bent its elbows, this would cause the forearms to move inward, towards its midline. It may have used that ability to grasp prey with both hands simultaneously.

Diet

Henry Fairfield Osborn, in his 1903 description of ''Ornitholestes'', noted its large and conical front teeth, the "rapid grasping power" of its hand, and the "balancing power" of its tail; these he interpreted as adaptations to prey on contemporary birds. Osborn later repudiated this hypothesis, suggesting in 1917 that ''Ornitholestes'' presented the early stages of a transition from a carnivorous to a more herbivorous lifestyle, but not before Charles R. Knight had drawn an influential and widely published illustration of ''Ornitholestes'' chasing ''Archaeopteryx''. Knight's illustration, and others derived from it, continued to appear in dinosaur books aimed at a popular audience throughout the 20th century.

David Norman (1985) conceded it was "just possible, though not very likely" that ''Ornitholestes'' might have caught and eaten primitive birds. Most recent authors, however, have instead suggested a diet of small terrestrial vertebrates. Mammals, lizards, frogs, salamanders, rhynchocephalians, and hatchling dinosaurs would all have been potential prey items. Gregory S. Paul (1988) thought that ''Ornitholestes'' might have used its conical front teeth to catch fish. Norman (1985) suggested that the robust skull and jaws might have allowed ''Ornitholestes'' to tackle "larger and more active prey" than other small theropods. In this vein, David Lambert (1993) speculated that ''Ornitholestes'', if it was a pack hunter, might have been able to "take on ornithopods as big as a half-grown '' Camptosaurus''."

In 2007, John Foster, a specialist on the Morrison Formation, suggested the possibility of niche partitioning between ''Ornitholestes'' and its contemporary ''Coelurus'', which was within the same size range.Foster (2007), p. 180 He theorized that big-eyed ''Ornitholestes'' might have been specialized for nocturnal hunting, while ''Coelurus'' may have focused on those prey species that were active during the day. Foster noted, however, that this hypothesis was largely speculative; a lack of preserved skull material from ''Coelurus'' makes it impossible to verify whether its eyes were proportionally smaller than those of ''Ornitholestes''.

Paul (1988) estimated that a endothermic ''Ornitholestes'' would have a daily dietary requirement of about of flesh.

Feathers

Ornithologist Percy Lowe hypothesized in 1944 that ''Ornitholestes'' might have borne feathers. However, this interpretation was largely disregarded for over half a century; most reconstructions of theropod dinosaurs, including ''Ornitholestes'', portrayed them with reptile-like scaly skin. One of the few exceptions to this was Gregory S. Paul's ''Predatory Dinosaurs of the World'' (1988). Robert T. Bakker's ''The Dinosaur Heresies'' (1986) accurately predicted the presence of feathers on dromaeosaurids and contended that all dinosaurs were endothermic, yet did not incorporate feathers in its illustration of ''Ornitholestes''.

In 1996, the primitive coelurosaur '' Sinosauropteryx'' was discovered in China. The well-preserved fossil showed that this dinosaur bore a coat of rudimentary furlike feathers. As a result of this and other similar discoveries, most paleontologists now consider it likely that all coelurosaurs had insulating feathers of some kind, or were descended from ancestors that did.Chatterjee and Templin (2004), p. 277; Fastovsky and Weishampel (2005), p. 329–330; Currie (2005), p. 368 Based on its phylogenetic position, John Foster (2007) inferred that the feathers of ''Ornitholestes'' would probably have been more primitive than those of birds; they likely "would have covered the body except the legs in a short coat, perhaps with longer feathers lining the top of the skull or neck and the back edge of the forearms."Foster (2007), p. 179 Assuming they were present, these feathers would have been used for insulation, and possibly also for brooding eggs.

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{{Taxonbar, from=Q14449

Prehistoric coelurosaurs
Late Jurassic dinosaurs of North America
Dinosaurs of the Morrison Formation
Fossil taxa described in 1903
Taxa named by Henry Fairfield Osborn
Paleontology in Wyoming