Ornitholestes

File:Ornitholestes Holotype AMNH.jpg

Ornitholestes was the first theropod to be discovered in the 1900s.Fastovsky and Weishampel (2005), p. 291 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.Paul D. Brinkman, 2010, The Second Jurassic Dinosaur Rush: Museums & Paleontology in America at the Turn of the Twentieth Century. University of Chicago Press, 345 pp., {{ISBN|978-0-226-07472-6}} 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.Osborn (1903), p. 459–464 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").Osborn (1903), p. 459; Osborn (1917), p. 733{{cite book |last1=Colbert |first1=Edwin H. (Edwin Harris) |last2=Knight |first2=Charles Robert |title=The dinosaur book: the ruling reptiles and their relatives |date=1951 |publisher=McGraw-Hill |location=New York |page=152 |url=https://archive.org/details/bookruli00colb/page/152/mode/2up}} 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.Osborn (1903), p. 459; Osborn (1917), p. 736 However, as Gregory S. Paul (1988) noted, the poor preservation of the corresponding elements in the type specimen made this association "tentative."Paul (1988b), p. 3 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.Carpenter et al. (2005b), p. 23, 39 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.Carpenter et al. (2005b), p. 39 Following this reassignment, Phil Senter (2006) noted that "our knowledge of Ornitholestes can be drawn now only from the holotype."Senter (2006), p. 1029 John Foster (2007) reported that some fragments from Dry Mesa Quarry may belong to Ornitholestes,Foster (2007), p. 78, 179 though these have not yet been described.

In 1920 Charles Whitney Gilmore concluded that Ornitholestes was identical to Coelurus;Gilmore, C.W., 1920, "Osteology of the carnivorous Dinosauria in the United States National Museum, with special reference to the genera Antrodemus (Allosaurus) and Ceratosaurus", Bulletin U.S. National Museum CX: 1-154 in 1934 Oliver Perry Hay recognised only a difference at the species level, naming a Coelurus hermanni,Hay, O.P., 1930, Second Bibliography and Catalogue of the Fossil Vertebrata of North America. Carnegie Institution of Washington. 390(II): 1-1074 but in 1980 John Ostrom revived the genus.Ostrom (1980)

File:Ornitholestes Scale.svg

In his 1903 description, Osborn wrote that the length of Ornitholestes along "the skull and vertebral column as restored" was {{Convert|2.22|m|ft|sigfig=3|abbr=on}}.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.Osborn (1917), p. 735; Paul (1988b), p. 3 David Norman (1985) and John Foster (2007) both estimated that Ornitholestes was about {{Convert|2|m|ft|sigfig=2|abbr=on}} long.Norman (1985), p. 39; Foster (2007), p. 178 Gregory S. Paul's 1988 Predatory Dinosaurs of the World listed the length of Ornitholestes as approximately {{Convert|2.08|m|ft|sigfig=3|abbr=on}}.Paul (1988a), p. 305 Paul (1988) and Foster (2007) both estimated that Ornitholestes weighed {{Convert|12.6|kg|lb|sigfig=3|abbr=on}}.Paul (1988a), p. 305; Foster (2007), p. 178 John A. Long and Peter Schouten (2008) suggested a slightly higher figure, {{Convert|15|kg|lb|sigfig=2|abbr=on}}.Long and Schouten (2008), p. 73

Ornitholestes was a bipedal carnivore.Lambert (1993), p. 79 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.Paul (1988a), p. 306; Norman (1985), p. 42; Norman (1990), p. 293 The orbits (eye sockets) were quite large, measuring over 25 percent of the skull's length.Osborn (1903), p. 460; Chure (1998), p. 238 There is no indication of a bony eye ring.Paul (1988b), p. 6

File:Ornitholestes reconstruction.png]]

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.Paul (1988b), p. 3; Norman (1990), p. 293 Henry Fairfield Osborn (1903) counted four teeth in the premaxilla, of which the front tooth was the largest in the upper jaw.Osborn (1903), p. 460; Osborn (1917), p. 734 In contrast, Gregory S. Paul (1988) depicted the skull with only three premaxillary teeth remaining, much smaller than those illustrated by Osborn.Paul (1988b), p. 4; Norman (1990), p. 293 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.Osborn (1903), p. 460 The tooth rows of Ornitholestes were short, with the dentary (lower) row being even shorter than the maxillary (upper) row,Paul (1988b), p. 3; Norman (1990), p. 292 even though the dentary bone itself was exceptionally long at the back, reaching a point below the middle of the eye socket.Cristiano dal Sasso & Simone Maganuco, 2011, Scipionyx samniticus (Theropoda: Compsognathidae) from the Lower Cretaceous of Italy — Osteology, ontogenetic assessment, phylogeny, soft tissue anatomy, taphonomy and palaeobiology, Memorie della Società Italiana de Scienze Naturali e del Museo Civico di Storia Naturale di Milano XXXVII(I): 1-281 Teeth did not extend as far back as the orbits, and neither tooth row spanned much more than one-third of the skull.Osborn (1903), p. 460; Norman (1990), p. 293

File:Ornitholestes skull.jpg

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.Rauhut (2003), p. 27; Carpenter et al. (2005a), p. 53 Paul's updated illustration of Ornitholestes in his 2010 Princeton Field Guide to Dinosaurs no longer contains the nasal horn.Paul (2010), p. 123

File:Ornitholestes hand.jpg

Ornitholestes had a relatively short neck with a slight sigmoidal (S-shaped) curve.Carpenter et al. (2005a), pp. 49, 54 The tail was long and whiplike, comprising over half of the body's length.Osborn (1917), p. 734; Lambert (1993), p. 78 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.Osborn (1917), p. 735–736 Carpenter et al. (2005a) recorded that the specimen contained five sacral vertebrae.Carpenter et al. (2005a), p. 58 Ornitholestes was a short-bodied theropod, and this was reflected in the short front-to-back dimensions of the cervical and dorsal vertebrae.Carpenter et al. (2005a), p. 49, 69

The forelimbs of Ornitholestes were relatively long, slightly under two-thirds the length of the hind legs.Ostrom (1969), p. 146; Paul (2002), p. 236 The humerus (upper arm bone) was heavily built, and somewhat longer than the radius and ulna (forearm bones).Osborn (1917), p. 738; Carpenter et al. (2005b), p. 45 Both the humerus and radius were straight-shafted.Carpenter et al. (2005a), p. 60, 62 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.Paul (1988a), p. 306 Osborn (1917) calculated that the, missing, tibia (shin bone) was only about 70.6% as long as the femur (thigh bone).Osborn (1917), p. 737 The metatarsals (foot bones) were spaced closely, but not fused together.Carpenter et al. (2005a), p. 67 As is typical of theropods, the feet were tridactyl (with three clawed weight-bearing toes).Osborn (1903), p. 463 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.Ostrom (1969), p. 161 However, as both Ostrom (1969) and Paul (1988) noted, the poor preservation of digit II makes this hypothesis difficult to confirm.Ostrom (1969), p. 161; Paul (1988b), p. 6

The infraorder Coelurosauria, coined in 1914 by Friedrich von Huene, was traditionally a taxonomic wastebasket into which all small theropods were placed.Paul (1988a), p. 188–189; Norman (1990), p. 280 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.Holtz et al. (2004), p. 71 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.Paul (1988a), p. 302; Paul (1988b), p. 3, 6 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.Paul (2010), p. 124 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.{{Cite journal | last1 = Godefroit | first1 = Pascal | last2 = Cau| first2 = Andrea | last3 = Hu | first3 = Dong-Yu| last4 = Escuillié | first4 = François| last5 = Wu | first5 = Wenhao| last6 = Dyke | first6 = Gareth| doi = 10.1038/nature12168 | title = A Jurassic avialan dinosaur from China resolves the early phylogenetic history of birds | journal = Nature | volume = 498| issue = 7454| pages =359–362| year = 2013 | pmid = 23719374| bibcode = 2013Natur.498..359G | s2cid = 4364892 }}

File:Ornitholestesskeleton.JPG, which stands much the same today]]

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.

{{clade| style=font-size:100%;line-height:80%

|label1=Coelurosauria

|1={{clade

|1=†Bicentenaria

|2={{clade

|1=†Zuolong 100 px

|label2=Tyrannoraptora

|2={{clade

|1=†Tyrannosauroidea100 px

|label2={{color|white|unnamed}}

|2={{clade

|1=†Aorun

|2={{clade

|1=†Scipionyx

|2={{clade

|1=†Ornitholestes100 px

|2={{clade

|1=†Compsognathidae

|label2=Maniraptoriformes

|2={{clade

|1=†Ornithomimosauria100 px

|2=Maniraptora100px

}} }} }} }} }} }} }} }} }}In an abstract presented at the 2021 conference of the Society of Vertebrate Paleontology, Kimberley Chapelle and colleagues found "robust evidence" that Ornitholestes is the earliest-diverging oviraptorosaur, based on a CT scan analysis of the skull.{{Cite journal |last1=Chapelle |first1=Kimberley E. |last2=Norell |first2=Mark |last3=Ford |first3=David P. |last4=Hendrickx |first4=Christophe |last5=Radermacher |first5=Viktor J. |last6=Balanoff |first6=Amy |last7=Zanno |first7=Lindsay E. |last8=Choiniere |first8=Jonah N. |date=2021 |title=A CT-based revised description and phylogenetic analysis of the skull of the basal maniraptoran Ornitholestes hermanni Osborn 1903 |url=https://ri.conicet.gov.ar/handle/11336/202364 |journal=Conference Program of the 81st Annual Meeting of the Society of Vertebrate Paleontology}}

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.

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 (2006), p. 1029–1030 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.Senter (2006), p. 1032

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.Senter (2006), p. 1030–1032 It may have used that ability to grasp prey with both hands simultaneously.Senter (2006), p. 1031

File:The American Museum journal (c1900-(1918)) (17537482124).jpg portrays Ornitholestes hunting Archaeopteryx, though they were not contemporaries]]

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.Osborn (1917), p. 733–734; Glut (1997), p. 645 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.Norman (1985), p. 39 Most recent authors, however, have instead suggested a diet of small terrestrial vertebrates. Frogs, salamanders, mammals, lizards, rhynchocephalians, and hatchling dinosaurs would all have been potential prey items.Norman (1985), p. 39; Paul (1988), p. 306; Foster (2007), p. 179; Long and Schouten (2008), p. 73 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.Norman (1985), p. 42 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."Lambert (1993), p. 78

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.Foster (2007), p. 180–181

Paul (1988) estimated that a {{Convert|12|kg|lb|sigfig=2|abbr=on}} endothermic Ornitholestes would have a daily dietary requirement of about {{Convert|700|g|lb|sigfig=3|abbr=on}} of flesh.Paul (1988a), p. 404

Ornithologist Percy Lowe hypothesized in 1944 that Ornitholestes might have borne feathers.Witmer (1992), p. 444 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).Paul (1988a), p. 122–123, 211 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.Bakker (1986), p. 99, 310

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.

{{Reflist|colwidth=30em}}

{{Portal|Dinosaurs}}

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{{Theropoda|O.}}

{{Taxonbar|from=Q14449}}

Category:Coelurosauria

Category:Dinosaurs of the Morrison Formation

Category:Fossil taxa described in 1903

Category:Taxa named by Henry Fairfield Osborn

Category:Paleontology in Wyoming