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Along with ''[[Tyrannosaurus]]'', ''Allosaurus'' has come to represent the quintessential large, carnivorous dinosaur in popular culture. It is a common dinosaur in museums, due in particular to the excavations at the Cleveland Lloyd Dinosaur Quarry; by 1976, as a result of cooperative operations, 38&nbsp;museums in eight countries on three continents had Cleveland-Lloyd allosaur material or casts.<ref name=JM76/> ''Allosaurus'' is the official [[state fossil]] of Utah.<ref name=statefossil>{{cite web |url=http://pioneer.utah.gov/utah_on_the_web/utah_symbols/fossil.html |title=Utah Symbols – State Fossil |accessdate=2007-09-30|publisher=State of Utah }}</ref>
Along with ''[[Tyrannosaurus]]'', ''Allosaurus'' has come to represent the quintessential large, carnivorous dinosaur in popular culture. It is a common dinosaur in museums, due in particular to the excavations at the Cleveland Lloyd Dinosaur Quarry; by 1976, as a result of cooperative operations, 38&nbsp;museums in eight countries on three continents had Cleveland-Lloyd allosaur material or casts.<ref name=JM76/> ''Allosaurus'' is the official [[state fossil]] of Utah.<ref name=statefossil>{{cite web |url=http://pioneer.utah.gov/utah_on_the_web/utah_symbols/fossil.html |title=Utah Symbols – State Fossil |accessdate=2007-09-30|publisher=State of Utah }}</ref>


''Allosaurus'' has been depicted in popular culture since the early years of the 20th century. It is top predator in both [[Arthur Conan Doyle]]'s 1912 novel, ''[[The Lost World (Conan Doyle novel)|The Lost World]]'', and its [[The Lost World (1925 film)|1925 film adaptation]], the first full-length motion picture to feature dinosaurs.<ref>Glut, Donald F.; Brett-Surman, Michael K. (1997). "Dinosaurs and the media", in Farlow, James; and Brett-Surman, Michael K. (eds.): The Complete Dinosaur. Bloomington and Indianapolis: Indiana University Press, 675–706. ISBN 0-253-33349-0.</ref> It later became the starring dinosaur of the 1956 film ''[[The Beast of Hollow Mountain]]'',<ref name=DL90>Lambert, ''Dinosaur Data Book'', p. 299.</ref> and the 1969 film ''[[The Valley of Gwangi]]'', two [[genre]] combinations of living dinosaurs with [[Western (genre)|Westerns]]. In ''The Valley of Gwangi'', Gwangi is billed as an ''Allosaurus'', although [[Ray Harryhausen]] based his model for the creature on Charles R. Knight's depiction of a ''Tyrannosaurus''. Harryhausen sometimes confuses the two, stating in a DVD interview "They're both meat eaters, they're both tyrants... one was just a bit larger than the other."<ref>''Return to the Valley'', a documentary on the Region 1 ''Valley of Gwangi'' DVD.</ref> ''Allosaurus'' also made appearances in the [[Hammer Film Productions|Hammer]] 1966 remake ''[[One Million Years B.C.]]'' and the 1975 film adaptation of ''[[The Land That Time Forgot (film)|The Land that Time Forgot]]''. In nonfictional presentations, ''Allosaurus'' appears in the second and fifth episodes of the [[BBC]] television series ''[[Walking with Dinosaurs]]'', ''[[Jurassic Fight Club]]'', and the ''Walking with Dinosaurs'' special ''[[The Ballad of Big Al]]'' which chronicles the life of the ''Allosaurus'' specimen nicknamed "Big Al".
''Allosaurus'' has been depicted in popular culture since the early years of the 20th century. It is top predator in both [[Arthur Conan Doyle]]'s 1912 novel, ''[[The Lost World (Conan Doyle novel)|The Lost World]]'', and its [[The Lost World (1925 film)|1925 film adaptation]], the first full-length motion picture to feature dinosaurs.<ref>Glut, Donald F.; Brett-Surman, Michael K. (1997). "Dinosaurs and the media", in Farlow, James; and Brett-Surman, Michael K. (eds.): The Complete Dinosaur. Bloomington and Indianapolis: Indiana University Press, 675–706. ISBN 0-253-33349-0.</ref> It later became the starring dinosaur of the 1956 film ''[[The Beast of Hollow Mountain]]'',<ref name=DL90>Lambert, ''Dinosaur Data Book'', p. 299.</ref> and the 1969 film ''[[The Valley of Gwangi]]'', two [[genre]] combinations of living dinosaurs with [[Western (genre)|Westerns]]. In ''The Valley of Gwangi'', Gwangi is billed as an ''Allosaurus'', although [[Ray Harryhausen]] based his model for the creature on Charles R. Knight's depiction of a ''Tyrannosaurus''. Harryhausen sometimes confuses the two, stating in a DVD interview "They're both meat eaters, they're both tyrants... one was just a bit larger than the other."<ref>''Return to the Valley'', a documentary on the Region 1 ''Valley of Gwangi'' DVD.</ref> ''Allosaurus'' also made appearances in the [[Hammer Film Productions|Hammer]] 1966 remake ''[[One Million Years B.C.]]'' and the 1975 film adaptation of ''[[The Land That Time Forgot (film)|The Land that Time Forgot]]''. In nonfictional presentations, ''Allosaurus'' appears in the second and fifth episodes of the [[BBC]] television series ''[[Walking with Dinosaurs]]'', ''[[Jurassic Fight Club]]'', and the ''Walking with Dinosaurs'' special ''[[The Ballad of Big Al]]'' which chronicles the life of the ''Allosaurus'' specimen nicknamed "Big Al". [[Iron Maiden]], [[Slayer]], [[*Britney Spears*]]


==References==
==References==

Revision as of 00:58, 13 November 2009

Allosaurus
Temporal range: Late Jurassic, 155–145 Ma
Mounted A. fragilis skeleton, San Diego Natural History Museum
Scientific classification
Kingdom:
Animalia
Phylum:
Chordata
Class:
Reptilia
Superorder:
Dinosauria
Order:
Saurischia
Suborder:
Theropoda
Infraorder:
†Carnosauria
Family:
†Allosauridae
Genus:
†Allosaurus

Marsh, 1877
Species
  • A. fragilis Marsh, 1877 (type)
  • ?A. europaeus Mateus et al., 2006
  • A. "jimmadseni" Chure, 2000 vide Glut, 2003 (nomen nudum)
  • ?A. tendagurensis Janensch, 1925
Synonyms

Allosaurus (Template:Pron-en) is a genus of large theropod dinosaur that lived 155 to 145 million years ago, in the late Jurassic period (Kimmeridgian to Tithonian). The name Allosaurus means "different lizard" and is derived from the Greek αλλος/allos ("different, strange") and σαυρος/sauros ("lizard"). The first remains that can definitely be ascribed to this genus were described in 1877 by Othniel Charles Marsh. As one of the first well-known theropod dinosaurs, it has long attracted attention outside of paleontological circles, and has been a lead dinosaur in several films and documentaries.

Allosaurus was a large bipedal predator with a large skull, equipped with dozens of large, sharp teeth. It averaged 8.5 meters (28 ft) in length, though fragmentary remains suggest it could have reached over 12 meters (39 ft). Relative to the large and powerful hindlimbs, its three-fingered forelimbs were small, and the body was balanced by a long, heavy tail. It is classified as an allosaurid, a type of carnosaurian theropod dinosaur. The genus has a complicated taxonomy, and includes an uncertain number of valid species, the best known of which is A. fragilis. The bulk of Allosaurus remains have come from North America's Morrison Formation, with material also known from Portugal and possibly Tanzania. It was known for over half of the 20th century as Antrodemus, but study of the copious remains from the Cleveland Lloyd Dinosaur Quarry brought the name Allosaurus back to prominence, and established it as one of the best-known dinosaurs.

As the prominent large predator in the Morrison Formation, Allosaurus was at the top of the food chain, probably preying on contemporaneous large herbivorous dinosaurs and perhaps even other predators (e.g Ceratosaurus). Potential prey included ornithopods, stegosaurids, and sauropods. Some paleontologists interpret Allosaurus as having had cooperative social behavior, and hunting in packs, while others believe individuals may have been aggressive toward each other, and that congregations of this genus are the result of lone individuals feeding on the same carcasses. It may have attacked large prey by ambush, using its upper jaws like a hatchet.

Description

The size range of Allosaurus, compared with a human.

Allosaurus was a typical large theropod, having a massive skull on a short neck, a long tail and reduced forelimbs. Allosaurus fragilis, the best-known species, had an average length of 8.5 meters (28 ft),[1] with the largest definitive Allosaurus specimen (AMNH 680) estimated at 9.7 meters long (32 ft),[2] and an estimated weight of 2.3 metric tons (2.5 short tons).[2] In his 1976 monograph on Allosaurus, James Madsen mentioned a range of bone sizes which he interpreted to show a maximum length of 12 to 13 meters (40 to 43 ft).[3] As with dinosaurs in general, weight estimates are debatable, and since 1980 have ranged between 1500 kilograms (3300 lb), 1000 to 4000 kilograms (2200 to 8800 lb), and 1010 kilograms (2230 lb) for modal adult weight (not maximum).[4] John Foster, a specialist on the Morrison Formation, suggests that 1000 kg (2200 lb) is reasonable for large adults of A. fragilis, but that 700 kg (1500 lb) is a closer estimate for individuals represented by the average-sized thigh bones he has measured.[5]

Several gigantic specimens have been attributed to Allosaurus, but may in fact belong to other genera. The closely related genus Saurophaganax (OMNH 1708) reached perhaps 10.9 meters (36 ft) in length,[2] and its single species has sometimes been included in the genus Allosaurus as Allosaurus maximus, though recent studies support it as a separate genus.[6] Another potential specimen of Allosaurus, once assigned to the genus Epanterias (AMNH 5767), may have measured 12.1 meters in length (40 ft).[2] A more recent discovery is a partial skeleton from the Peterson Quarry in Morrison rocks of New Mexico; this large allosaurid may be another individual of Saurophaganx.[7]

Skull

Skull cast, Oklahoma Museum of Natural History

The skull and teeth of Allosaurus were modestly proportioned for a theropod of its size. Paleontologist Gregory S. Paul gives a length of 845 millimeters (33.3 in) for a skull belonging to an individual he estimates at 7.9 meters long (26 ft).[8] Each premaxilla (the bones that formed the tip of the snout), held five teeth with D-shaped cross-sections, and each maxilla (the main tooth-bearing bones in the upper jaw) had between fourteen and seventeen teeth; the number of teeth does not exactly correspond to the size of the bone. Each dentary (the tooth-bearing bone of the lower jaw) had between fourteen and seventeen teeth, with an average count of sixteen. The teeth became shorter, more narrow, and more curved toward the back of the skull. All of the teeth had saw-like edges. They were shed easily, and were replaced continually, making them common fossils.[3]

The skull had a pair of horns above and in front of the eyes. These horns were composed of extensions of the lacrimal bones,[3] and varied in shape and size. There were also lower paired ridges running along the top edges of the nasal bones that led into the horns.[3] The horns were probably covered in a keratin sheath and may have had a variety of functions, including acting as sunshades for the eye,[3] being used for display, and being used in combat against other members of the same species[8][9] (although they were fragile).[3] There was a ridge along the back of the skull roof for muscle attachment, as is also seen in tyrannosaurids.[8]

Inside the lacrimal bones were depressions that may have held glands, such as salt glands.[10] Within the maxillae were sinuses that were better developed than those of more basal theropods such as Ceratosaurus and Marshosaurus; they may have been related to the sense of smell, perhaps holding something like Jacobson's organ. The roof of the braincase was thin, perhaps to improve thermoregulation for the brain.[3] The skull and lower jaws had joints that permitted motion within these units. In the lower jaws, the bones of the front and back halves loosely articulated, permitting the jaws to bow outward and increasing the animal's gape.[11] The braincase and frontals may also have had a joint.[3]

Postcranial skeleton

Mounted A. fragilis specimen (AMNH 5753)

Allosaurus had nine vertebrae in the neck, fourteen in the back, and five in the sacrum supporting the hips.[12] The number of tail vertebrae is unknown and varied with individual size; James Madsen estimated about 50,[3] while Gregory S. Paul considered that to be too many and suggested 45 or less.[8] There were hollow spaces in the neck and anterior back vertebrae.[3] Such spaces, which are also found in modern theropods (that is, the birds), are interpreted as having held air sacs used in respiration.[13] The rib cage was broad, giving it a barrel chest, especially in comparison to less derived theropods like Ceratosaurus.[14] Allosaurus had gastralia (belly ribs), but these are not common findings,[3] and they may have ossified poorly.[8] In one published case, the gastralia show evidence of injury during life.[15] A furcula (wishbone) was also present, but has only been recognized since 1996; in some cases furculae were confused with gastralia.[15][16] The ilium, the main hip bone, was massive, and the pubic bone had a prominent foot that may have been used for both muscle attachment and as a prop for resting the body on the ground. Madsen noted that in about half of the individuals from the Cleveland Lloyd Dinosaur Quarry, independent of size, the pubes had not fused to each other at their foot ends. He suggested that this was a sexual characteristic, with females lacking fused bones to make egg-laying easier.[3] This proposal has not attracted further attention, however.

Hand and claws of A. fragilis

The forelimbs of Allosaurus were short in comparison to the hindlimbs (only about 35% the length of the hindlimbs in adults)[17] and had three fingers per hand, tipped with large, strongly curved and pointed claws.[3] The arms were powerful,[8] and the forearm was somewhat shorter than the upper arm (1:1.2 humerus/ulna ratio).[18] The wrist had a version of the semilunate carpal[19] also found in more derived theropods like maniraptorans. Of the three fingers, the innermost (or thumb) was the largest,[8] and diverged from the others.[18] The legs were not as long or suited for speed as those of tyrannosaurids, and the claws of the toes were less developed and more hoof-like than those of earlier theropods.[8] Each foot had three weight-bearing toes and an inner dewclaw, which Madsen suggested could have been used for grasping in juveniles.[3] There was also what is interpreted as the splint-like remnant of a fifth (outermost) metatarsal, perhaps used as a lever between the Achilles tendon and foot.[20]

Classification

Life restoration of Allosaurus fragilis.

Allosaurus was an allosaurid, a member of a family of large theropods within the larger group Carnosauria. The family name Allosauridae was created for this genus in 1878 by Othniel Charles Marsh,[21] but the term was largely unused until the 1970s in favor of Megalosauridae, another family of large theropods that eventually became a wastebasket taxon. This, along with the use of Antrodemus for Allosaurus during the same period, is a point that needs to be remembered when searching for information on Allosaurus in publications that predate James Madsen's 1976 monograph. Major publications using the name Megalosauridae instead of Allosauridae include Gilmore, 1920,[18] von Huene, 1926,[22] Romer, 1956 and 1966,[23][24] Steel, 1970,[25] and Walker, 1964.[26]

Following the publication of Madsen's influential monograph, Allosauridae became the preferred family assignment, but it too was not strongly defined. Semi-technical works used Allosauridae for a variety of large theropods, usually those that were larger and better-known than megalosaurids. Typical theropods that were thought to be related to Allosaurus included Indosaurus, Piatnitzkysaurus, Piveteausaurus, Yangchuanosaurus,[27] Acrocanthosaurus, Chilantaisaurus, Compsosuchus, Stokesosaurus, and Szechuanosaurus.[28] Given modern knowledge of theropod diversity and the advent of cladistic study of evolutionary relationships, none of these theropods is now recognized as an allosaurid, although several, like Acrocanthosaurus and Yangchuanosaurus, are members of closely related families.[13]

Allosauridae is one of three families in Carnosauria; the other two are Carcharodontosauridae and Sinraptoridae.[13] Allosauridae has at times been proposed as ancestral to the Tyrannosauridae (which would make it paraphyletic), one recent example in Gregory S. Paul's Predatory Dinosaurs of the World,[29] but this has been rejected, with tyrannosaurids identified as members of a separate branch of theropods, the Coelurosauria.[30] Allosauridae is the smallest of the carnosaur families, with only Saurophaganax and a currently unnamed French allosauroid accepted as possible valid genera besides Allosaurus in the most recent review.[13] Another genus, Epanterias, is a potential valid member, but it and Saurophaganax may turn out to be large examples of Allosaurus.[8] Recent reviews have kept the genus Saurophaganax and included Epanterias with Allosaurus.[4][13]

Discovery and history

Early discoveries and research

The discovery and early study of Allosaurus is complicated by the multiplicity of names coined during the Bone Wars of the late 1800s. The first described fossil in this history was a bone obtained secondhand by Ferdinand Vandiveer Hayden in 1869. It came from Middle Park, near Granby, Colorado, probably from Morrison Formation rocks. The locals had identified such bones as "petrified horse hoofs". Hayden sent his specimen to Joseph Leidy, who identified it as half of a tail vertebra, and tentatively assigned it to the European dinosaur genus Poekilopleuron as Poicilopleuron [sic] valens.[31] He later decided it deserved its own genus, Antrodemus.[32]

The skeletal mount of AMNH 5753, posed as scavenging an Apatosaurus.
AMNH 5753 in a Charles R. Knight life restoration.

Allosaurus itself is based on YPM 1930, a small collection of fragmentary bones including parts of three vertebrae, a rib fragment, a tooth, a toe bone, and, most useful for later discussions, the shaft of the right humerus (upper arm). Othniel Charles Marsh gave these remains the formal name Allosaurus fragilis in 1877. Allosaurus comes from the Greek allos/αλλος, meaning "strange" or "different" and saurus/σαυρος, meaning "lizard" or "reptile".[33] It was named 'different lizard' because its vertebrae were different from those of other dinosaurs known at the time of its discovery.[34][35] The species epithet fragilis is Latin for "fragile", referring to lightening features in the vertebrae. The bones were collected from the Morrison Formation of Garden Park, north of Cañon City.[34] Marsh and Edward Drinker Cope, who were in scientific competition, went on to coin several other genera based on similarly sparse material that would later figure in the taxonomy of Allosaurus. These include Marsh's Creosaurus[21] and Labrosaurus,[36] and Cope's Epanterias.[37]

In their haste, Cope and Marsh did not always follow up on their discoveries (or, more commonly, those made by their subordinates). For example, after the discovery by Benjamin Mudge of the type specimen of Allosaurus in Colorado, Marsh elected to concentrate work in Wyoming; when work resumed at Garden Park in 1883, M. P. Felch found an almost complete Allosaurus and several partial skeletons.[10] In addition, one of Cope's collectors, H. F. Hubbell, found a specimen in the Como Bluff area of Wyoming in 1879, but apparently did not mention its completeness, and Cope never unpacked it. Upon unpacking in 1903 (several years after Cope had died), it was found to be one of the most complete theropod specimens then known, and in 1908 the skeleton, now cataloged as AMNH 5753, was put on public view.[38] This is the well-known mount poised over a partial Apatosaurus skeleton as if scavenging it, illustrated as such by Charles R. Knight. Although notable as the first free-standing mount of a theropod dinosaur, and often illustrated and photographed, it has never been scientifically described.[39]

Mounted A. fragilis skeleton (USNM4734) found by Gilmore, at the National Museum of Natural History

The multiplicity of early names complicated later research, with the situation compounded by the terse descriptions provided by Marsh and Cope. Even at the time, authors such as Samuel Wendell Williston suggested that too many names had been coined.[40] For example, Williston pointed out in 1901 that Marsh had never been able to adequately distinguish Allosaurus from Creosaurus.[41] The most influential early attempt to sort out the convoluted situation was produced by Charles W. Gilmore in 1920. He came to the conclusion that the tail vertebra dubbed Antrodemus by Leidy was indistinguishable from those of Allosaurus, and Antrodemus thus should be the preferred name because as the older name it had priority.[18] Antrodemus became the accepted name for this familiar genus for over fifty years, until James Madsen published on the Cleveland-Lloyd specimens and concluded that Allosaurus should be used because Antrodemus was based on material with poor, if any, diagnostic features and locality information (for example, the geological formation that the single bone of Antrodemus came from is unknown).[3] "Antrodemus" has been used informally for convenience when distinguishing between the skull Gilmore restored and the composite skull restored by Madsen.[42]

Cleveland-Lloyd discoveries

Although sporadic work at what became known as the Cleveland-Lloyd Dinosaur Quarry in Emery County, Utah had taken place as early as 1927, and the fossil site itself described by William J. Stokes in 1945,[43] major operations did not begin there until 1960. Under a cooperative effort involving nearly 40 institutions, thousands of bones were recovered between 1960 and 1965.[3] The quarry is notable for the predominance of Allosaurus remains, the condition of the specimens, and the lack of scientific resolution on how it came to be. The majority of bones belong to the large theropod Allosaurus fragilis (it is estimated that the remains of at least 46 A. fragilis have been found there, out of at minimum 73 dinosaurs), and the fossils found there are disarticulated and well-mixed. Nearly a dozen scientific papers have been written on the taphonomy of the site, coming up with numerous contradictory explanations for how it formed. Suggestions have ranged from animals getting stuck in a bog, to becoming trapped in deep mud, to falling victim to drought-induced mortality around a waterhole, to getting trapped in a spring-fed pond or seep.[44] Regardless of the actual cause, the great quantity of well-preserved Allosaurus remains has allowed this genus to be known in detail, making it among the best-known theropods. Skeletal remains from the quarry pertain to individuals of almost all ages and sizes, from less than 1 meter (3.3 ft)[45] to 12 meters (39 ft) long, and the disarticulation is an advantage for describing bones usually found fused.[3]

Recent work: 1980s–present

The period since Madsen's monograph has been marked by a great expansion in studies dealing with topics concerning Allosaurus in life (paleobiological and paleoecological topics). Such studies have covered topics including skeletal variation,[46] growth,[47][48] skull construction,[49] hunting methods,[50] the brain,[51] and the possibility of gregarious living and parental care.[52] Reanalysis of old material (particularly of large 'allosaur' specimens),[8][53] new discoveries in Portugal,[54] and several very complete new specimens[15][55][56] have also contributed to the growing knowledge base. Fossil footprints attributed to Allosaurus were discovered in Bałtów, Poland, by Polish paleontologist Gerard Gierliński in the early 2000s.[57]

"Big Al"

Cast of "Big Al Two"

One of the more significant Allosaurus finds was the 1991 discovery of "Big Al" (MOR 693), a 95% complete, partially articulated specimen that measured about 8 meters (about 26 ft) in length. MOR 693 was excavated near Shell, Wyoming, by a joint Museum of the Rockies and University of Wyoming Geological Museum team.[58] This skeleton was discovered by a Swiss team, led by Kirby Siber. The same team later excavated a second Allosaurus, "Big Al Two", which is the best preserved skeleton of its kind to date.[56]

The completeness, preservation, and scientific importance of this skeleton gave "Big Al" its name; the individual itself was below the average size for Allosaurus fragilis,[58] and was a subadult estimated at only 87% grown.[59] The specimen was described by Breithaupt in 1996.[55] Nineteen of its bones were broken or showed signs of infection, which may have contributed to "Big Al's" death. Pathologic bones included five ribs, five vertebrae, and four bones of the feet; several damaged bones showed osteomyelitis, a bone infection. A particular problem for the living animal was infection and trauma to the right foot that probably affected movement and may have also predisposed the other foot to injury because of a change in gait.[59]

Species and taxonomy

Main article: Species of Allosaurus

It is unclear how many species of Allosaurus there were. Seven species have been considered potentially valid since 1988 (A. amplexus,[8] A. atrox,[8] A. europaeus,[60] the type species A. fragilis,[13] the as-yet not formally described "A. jimmadseni",[6] A. maximus,[46] and A. tendagurensis[13]), although only a fraction are usually considered valid at any given time. Additionally, there are at least ten dubious or undescribed species that have been assigned to Allosaurus over the years, along with the species belonging to genera now sunk into Allosaurus. In the most recent review of basal tetanuran theropods, only A. fragilis (including A. amplexus and A. atrox as synonyms), "A. jimmadseni" (as an unnamed species), and A. tendagurensis were accepted as potentially valid species, with A. europaeus not yet proposed and A. maximus assigned to Saurophaganax.[13]

Allosaurus sp. skull (DINO 11541) from Dinosaur National Monument, still partially encased in matrix.

A. amplexus, A. atrox, A. fragilis, "A. jimmadseni", and A. maximus are all known from remains discovered in the Kimmeridgian–Tithonian Upper Jurassic-age Morrison Formation of the United States, spread across the states of Colorado, Montana, New Mexico, Oklahoma, South Dakota, Utah, and Wyoming. A. fragilis is regarded as the most common, known from the remains of at least sixty individuals.[13] Debate has gone on since the 1980s regarding the possibility that there are two common Morrison Formation species of Allosaurus, with the second known as A. atrox;[8][61] recent work has followed a "one species" interpretation,[13] with the differences seen in the Morrison Formation material attributed to individual variation.[62][63] A. europaeus was found in the Kimmeridgian-age Porto Novo Member of the Lourinhã Formation,[60] but may be the same as A. fragilis.[64] A. tendagurensis was found in Kimmeridgian-age rocks of Tendaguru, in Mtwara, Tanzania.[65] Although the most recent review tentatively accepted it as a valid species of Allosaurus, it may be a more basal tetanuran,[66] or simply a dubious theropod.[1] Although obscure, it was a large theropod, possibly around 10 meters long (33 ft) and 2.5 metric tons (2.8 short tons) in weight.[2]

Allosaurus is regarded as a probable synonym of the genera Antrodemus, Creosaurus, Epanterias, and Labrosaurus.[13] Most of the species that are regarded as synonyms of A. fragilis, or that were misassigned to the genus, are obscure and were based on scrappy remains. One exception is Labrosaurus ferox, named in 1884 by Marsh for an oddly formed partial lower jaw, with a prominent gap in the tooth row at the tip of the jaw, and a rear section greatly expanded and turned down.[67] Later researchers suggested that the bone was pathologic, showing an injury to the living animal,[18] and that part of the unusual form of the rear of the bone was due to plaster reconstruction.[68] It is now regarded as an example of A. fragilis.[13] Other remains thought to pertain to Allosaurus have come from across the world, including Australia,[69] Siberia,[70] and Switzerland,[1] but these fossils have been reassessed as belonging to other dinosaurs.

Paleoecology

Locations in the Morrison Formation (yellow) where Allosaurus remains have been found.

Allosaurus was the most common large theropod in the vast tract of Western American fossil-bearing rock known as the Morrison Formation, accounting for 70 to 75% of theropod specimens,[5] and as such was at the top trophic level of the Morrison food web.[71] The Morrison Formation is interpreted as a semiarid environment with distinct wet and dry seasons, and flat floodplains.[72] Vegetation varied from river-lining forests of conifers, tree ferns, and ferns, to fern savannas with rare trees.[73]

The Morrison Formation has been a rich fossil hunting ground, holding fossils of green algae, fungi, mosses, horsetails, ferns, cycads, ginkgoes, and several families of conifers. Other fossils discovered include bivalves, snails, ray-finned fishes, frogs, salamanders, turtles, sphenodonts, lizards, terrestrial and aquatic crocodylomorphans, several species of pterosaur, numerous dinosaur species, and early mammals such as docodonts, multituberculates, symmetrodonts, and triconodonts. Such dinosaurs as the theropods Ceratosaurus, Ornitholestes, and Torvosaurus, the sauropods Apatosaurus, Brachiosaurus, Camarasaurus, and Diplodocus, and the ornithischians Camptosaurus, Dryosaurus, and Stegosaurus are known from the Morrison.[74] The Late Jurassic formations of Portugal where Allosaurus is present are interpreted as having been similar to the Morrison but with a stronger marine influence. Many of the dinosaurs of the Morrison Formation are the same genera as those seen in Portuguese rocks (mainly Allosaurus, Ceratosaurus, Torvosaurus, and Apatosaurus), or have a close counterpart (Brachiosaurus and Lusotitan, Camptosaurus and Draconyx).[75]

Outcrop of the Brushy Basin Member of the Morrison Formation, west of Green River, Utah, on the Colorado Plateau.

Allosaurus coexisted with fellow large theropods Ceratosaurus and Torvosaurus in both the United States and Portugal,[75] The three appear to have had different ecological niches, based on anatomy and the location of fossils. Ceratosaurs and torvosaurs may have preferred to be active around waterways, and had lower, thinner bodies that would have given them an advantage in forest and underbrush terrains, whereas allosaurs were more compact, with longer legs, faster but less maneuverable, and seem to have preferred dry floodplains.[76] Ceratosaurus, better known than Torvosaurus, differed noticeably from Allosaurus in functional anatomy by having a taller, narrower skull with large, broad teeth.[42] Allosaurus was itself a potential food item to other carnivores, as illustrated by an Allosaurus pubic foot marked by the teeth of another theropod, probably Ceratosaurus or Torvosaurus. The location of the bone in the body (along the bottom margin of the torso and partially shielded by the legs), and the fact that it was among the most massive in the skeleton, indicates that the Allosaurus was being scavenged.[77]

Paleobiology

Life history

The wealth of Allosaurus fossils, from nearly all ages of individuals, allows scientists to study how the animal grew and how long its lifespan may have been. Remains may reach as far back in the lifespan as eggs—crushed eggs from Colorado have been suggested as those of Allosaurus.[1] Based on histological analysis of limb bones, the upper age limit for Allosaurus is estimated at 22 to 28 years, which is comparable to that of other large theropods like Tyrannosaurus. From the same analysis, its maximum growth appears to have been at age 15, with an estimated growth rate of about 150 kilograms (330 lb) per year.[47]

Medullary bone tissue, also found in dinosaurs as diverse as Tyrannosaurus and Tenontosaurus, has been found in at least one Allosaurus specimen, a shin bone from the Cleveland-Lloyd Quarry. Today, this bone tissue is only formed in female birds that are laying eggs, as it is used to supply calcium to shells. Its presence in the Allosaurus individual establishes sex and shows she had reached reproductive age. By counting growth lines, it was shown that she was 10 years old at death, so sexual maturity in Allosaurus was attained well before maximum growth and size.[78]

Mounted cast of a juvenile specimen, A. "jimmadseni", North American Museum of Ancient Life

The discovery of a juvenile specimen with a nearly complete hindlimb shows that the legs were relatively longer in juveniles, and the lower segments of the leg (shin and foot) were relatively longer than the thigh. These differences suggest that younger Allosaurus were faster and had different hunting strategies than adults, perhaps chasing small prey as juveniles, then becoming ambush hunters of large prey upon adulthood.[48] The thigh bone became thicker and wider during growth, and the cross-section less circular, as muscle attachments shifted, muscles became shorter, and the growth of the leg slowed. These changes imply that juvenile legs has less predictable stresses compared with adults, which would have moved with more regular forward progression.[79]

Feeding

Allosaurus and Stegosaurus skeletons, Denver Museum of Nature and Science

Paleontologists accept Allosaurus as an active predator of large animals. Sauropods seem to be likely candidates as both live prey and as objects of scavenging, based on the presence of scrapings on sauropod bones fitting allosaur teeth well and the presence of shed allosaur teeth with sauropod bones.[80] There is dramatic evidence for allosaur attacks on Stegosaurus, including an Allosaurus tail vertebra with a partially healed puncture wound that fits a Stegosaurus tail spike, and a Stegosaurus neck plate with a U-shaped wound that correlates well with an Allosaurus snout.[81] However, as Gregory Paul noted in 1988, Allosaurus was probably not a predator of fully grown sauropods, unless it hunted in packs, as it had a modestly sized skull and relatively small teeth, and was greatly outweighed by contemporaneous sauropods.[8] Another possibility is that it preferred to hunt juveniles instead of fully grown adults.[5][61] Research in the 1990s and 2000s may have found other solutions to this question. Robert T. Bakker, comparing Allosaurus to Cenozoic sabre-toothed carnivorous mammals, found similar adaptations, such as a reduction of jaw muscles and increase in neck muscles, and the ability to open the jaws extremely wide. Although Allosaurus did not have sabre teeth, Bakker suggested another mode of attack that would have used such neck and jaw adaptations: the short teeth in effect became small serrations on a saw-like cutting edge running the length of the upper jaw, which would have been driven into prey. This type of jaw would permit slashing attacks against much larger prey, with the goal of weakening the victim.[50]

Allosaurus attacking, based on the theories of Bakker (1998) and Rayfield et al. (2001).

Similar conclusions were drawn by another study using finite element analysis on an Allosaurus skull. According to their biomechanical analysis, the skull was very strong but had a relatively small bite force. By using jaw muscles only, it could produce a bite force of 805 to 2,148 N, less than the values for alligators (13,000 N), lions (4,167 N), and leopards (2,268 N), but the skull could withstand nearly 55,500 N of vertical force against the tooth row. The authors suggested that Allosaurus used its skull like a hatchet against prey, attacking open-mouthed, slashing flesh with its teeth, and tearing it away without splintering bones, unlike Tyrannosaurus, which is thought to have been capable of damaging bones. They also suggested that the architecture of the skull could have permitted the use of different strategies against different prey; the skull was light enough to allow attacks on smaller and more agile ornithopods, but strong enough for high-impact ambush attacks against larger prey like stegosaurids and sauropods.[49] Their interpretations were challenged by other researchers, who found no modern analogues to a hatchet attack and considered it more likely that the skull was strong to compensate for its open construction when absorbing the stresses from struggling prey.[82] The original authors noted that Allosaurus itself has no modern equivalent, that the tooth row is well-suited to such an attack, and that articulations in the skull cited by their detractors as problematic actually helped protect the palate and lessen stress.[83] Another possibility for handling large prey is that theropods like Allosaurus were "flesh grazers" which could take bites of flesh out of living sauropods that were sufficient to sustain the predator so it would not have needed to expend the effort to kill the prey outright. This strategy would also potentially have allowed the prey to recover and be fed upon in a similar way later.[13] An additional suggestion notes that ornithopods were the most common available dinosaurian prey, and that allosaurs may have subdued them by using an attack similar to that of modern big cats: grasping the prey with their forelimbs, and then making multiple bites on the throat to crush the trachea.[5] This is compatible with other evidence that the forelimbs were strong and capable of restraining prey.[19]

Allosaurus skull cast in front view at the Museum für Naturkunde, Berlin

Other aspects of feeding include the eyes, arms, and legs. The shape of the skull of Allosaurus limited potential binocular vision to 20° of width, slightly less than that of modern crocodilians. As with crocodilians, this may have been enough to judge prey distance and time attacks.[84] The similar wide field of view suggests that allosaurs, like modern crocodilians, were ambush hunters.[85] The arms, compared with those of other theropods, were suited for both grasping prey at a distance or clutching it close,[19] and the articulation of the claws suggests that they could have been used to hook things.[18] Finally, the top speed of Allosaurus has been estimated at 30 to 55 kilometers per hour (19 to 34 miles per hour).[86]

Social behavior

Allosaurus has long been regarded in the semitechnical and popular literature as an animal that preyed on sauropods and other large dinosaurs by hunting in groups.[10][27][61] Robert T. Bakker has extended social behavior to parental care, and has interpreted shed allosaur teeth and chewed bones of large prey animals as evidence that adult allosaurs brought food to lairs for their young to eat until they were grown, and prevented other carnivores from scavenging on the food.[52] However, there is actually little evidence of gregarious behavior in theropods,[13] and social interactions with members of the same species would have included antagonistic encounters, as shown by injuries to gastralia[15] and bite wounds to skulls (the pathologic lower jaw named Labrosaurus ferox is one such possible example). Such head-biting may have been a way to establish dominance in a pack or to settle territorial disputes.[87]

Although Allosaurus may have hunted in packs,[88] it has recently been argued that Allosaurus and other theropods had largely aggressive instead of cooperative interactions with other members of their own species. The study in question noted that cooperative hunting of prey much larger than an individual predator, as is commonly inferred for theropod dinosaurs, is rare among vertebrates in general, and modern diapsid carnivores (including lizards, crocodiles, and birds) very rarely cooperate to hunt in such a way. Instead, they are typically territorial and will kill and cannibalize intruders of the same species, and will also do the same to smaller individuals that attempt to eat before they do when aggregated at feeding sites. According to this interpretation, the accumulation of remains of multiple Allosaurus individuals at the same site, e.g. in the Cleveland-Lloyd quarry, are not due to pack hunting, but to the fact that Allosaurus individuals were drawn together to feed on other disabled or dead allosaurs, and were sometimes killed in the process. This could explain the high proportion of juvenile and subadult allosaurs present, as juveniles and subadults are disproportionally killed at modern group feeding sites of animals like crocodiles and komodo dragons. The same interpretation applies to Bakker's lair sites.[89] There is some evidence for cannibalism in Allosaurus, including Allosaurus shed teeth found among rib fragments, possible tooth marks on a shoulder blade,[90] and cannibalized allosaur skeletons among the bones at Bakker's lair sites.[76]

Brain and senses

The brain of Allosaurus, as interpreted from spiral CT scanning of an endocast, was more consistent with crocodilian brains than those of the other living archosaurs, birds. The structure of the vestibular apparatus indicates that the skull was held nearly horizontal, as opposed to strongly tipped up or down. The structure of the inner ear was like that of a crocodilian, and so Allosaurus probably could have heard lower frequencies best, and would have had trouble with subtle sounds. The olfactory bulbs were large and seem to have been well suited for detecting odors, although the area for evaluating smells was relatively small.[51]

Allosaurus model in Bałtów, Poland.

Along with Tyrannosaurus, Allosaurus has come to represent the quintessential large, carnivorous dinosaur in popular culture. It is a common dinosaur in museums, due in particular to the excavations at the Cleveland Lloyd Dinosaur Quarry; by 1976, as a result of cooperative operations, 38 museums in eight countries on three continents had Cleveland-Lloyd allosaur material or casts.[3] Allosaurus is the official state fossil of Utah.[91]

Allosaurus has been depicted in popular culture since the early years of the 20th century. It is top predator in both Arthur Conan Doyle's 1912 novel, The Lost World, and its 1925 film adaptation, the first full-length motion picture to feature dinosaurs.[92] It later became the starring dinosaur of the 1956 film The Beast of Hollow Mountain,[28] and the 1969 film The Valley of Gwangi, two genre combinations of living dinosaurs with Westerns. In The Valley of Gwangi, Gwangi is billed as an Allosaurus, although Ray Harryhausen based his model for the creature on Charles R. Knight's depiction of a Tyrannosaurus. Harryhausen sometimes confuses the two, stating in a DVD interview "They're both meat eaters, they're both tyrants... one was just a bit larger than the other."[93] Allosaurus also made appearances in the Hammer 1966 remake One Million Years B.C. and the 1975 film adaptation of The Land that Time Forgot. In nonfictional presentations, Allosaurus appears in the second and fifth episodes of the BBC television series Walking with Dinosaurs, Jurassic Fight Club, and the Walking with Dinosaurs special The Ballad of Big Al which chronicles the life of the Allosaurus specimen nicknamed "Big Al". Iron Maiden, Slayer, *Britney Spears*

References

  1. ^ a b c d Glut, Donald F. (1997). "Allosaurus". Dinosaurs: The Encyclopedia. Jefferson, North Carolina: McFarland & Co. pp. 105–117. ISBN 0-89950-917-7.
  2. ^ a b c d e Mortimer, Mickey (2003-07-21). "And the largest Theropod is..." The Dinosaur Mailing List. Retrieved 2007-09-08.
  3. ^ a b c d e f g h i j k l m n o p q r Madsen, James H., Jr. (1993) [1976]. Allosaurus fragilis: A Revised Osteology. Utah Geological Survey Bulletin 109 (2nd ed.). Salt Lake City: Utah Geological Survey.{{cite book}}: CS1 maint: multiple names: authors list (link)
  4. ^ a b Foster, John R. (2003). Paleoecological Analysis of the Vertebrate Fauna of the Morrison Formation (Upper Jurassic), Rocky Mountain Region, U.S.A. New Mexico Museum of Natural History and Science Bulletin 23. Albuquerque: New Mexico Museum of Natural History and Science. p. 37.
  5. ^ a b c d Foster, John (2007). "Allosaurus fragilis". Jurassic West: The Dinosaurs of the Morrison Formation and Their World. Bloomington, Indiana: Indiana University Press. pp. 170–176. ISBN 978-0-253-34870-8. OCLC 77830875.
  6. ^ a b Chure, Daniel J. (2000). A new species of Allosaurus from the Morrison Formation of Dinosaur National Monument (Utah–Colorado) and a revision of the theropod family Allosauridae. Ph.D. dissertation. Columbia University.
  7. ^ Foster, John. 2007. Jurassic West: the Dinosaurs of the Morrison Formation and Their World. Bloomington, Indiana:Indiana University Press. p. 117.
  8. ^ a b c d e f g h i j k l m n Paul, Gregory S. (1988). "Genus Allosaurus". Predatory Dinosaurs of the World. New York: Simon & Schuster. pp. 307–313. ISBN 0-671-61946-2.
  9. ^ Molnar, Ralph E. (1977). "Analogies in the evolution of combat and display structures in ornithopods and ungulates". Evolutionary Theory. 3: 165–190.
  10. ^ a b c Norman, David B. (1985). "'Carnosaurs'". The Illustrated Encyclopedia of Dinosaurs: An Original and Compelling Insight into Life in the Dinosaur Kingdom. New York: Crescent Books. pp. 62–67. ISBN 0-517-468905.
  11. ^ Paul, Gregory S. (1988). Predatory Dinosaurs of the World. 91 and Figure 4–5 (93).
  12. ^ Madsen, 1976; note that not everyone agrees on where the neck ends and the back begins, and some authors such as Gregory S. Paul interpret the count as ten neck and thirteen back vertebrae.
  13. ^ a b c d e f g h i j k l m n Holtz, Thomas R., Jr. (2004). Weishampel, David B.; Dodson, Peter; and Osmólska, Halszka (eds.) (ed.). The Dinosauria (2nd ed.). Berkeley: University of California Press. pp. 71–110. ISBN 0-520-24209-2. {{cite book}}: |editor= has generic name (help); Unknown parameter |coauthors= ignored (|author= suggested) (help)CS1 maint: multiple names: authors list (link)
  14. ^ Paul, Gregory S. (1988). Predatory Dinosaurs of the World. 277.
  15. ^ a b c d Chure, Daniel J. (2000). "Observations on the morphology and pathology of the gastral basket of Allosaurus, based on a new specimen from Dinosaur National Monument". Oryctos. 3: 39–37. ISSN 1290-4805.
  16. ^ Chure, Daniel J. (1996). "On the presence of furculae in some non-maniraptoran theropods". Journal of Vertebrate Paleontology. 16 (3): 573–577. {{cite journal}}: Unknown parameter |coauthors= ignored (|author= suggested) (help)
  17. ^ Middleton, Kevin M. (2000). "Theropod forelimb design and evolution" (PDF). Zoological Journal of the Linnean Society. 128: 149–187. doi:10.1006/zjls.1998.0193. Retrieved 2007-10-25. {{cite journal}}: Unknown parameter |coauthors= ignored (|author= suggested) (help)
  18. ^ a b c d e f Gilmore, Charles W. (1920). "Osteology of the carnivorous dinosauria in the United States National Museum, with special reference to the genera Antrodemus (Allosaurus) and Ceratosaurus". Bulletin of the United States National Museum. 110: 1–159.
  19. ^ a b c Carpenter, Kenneth (2002). "Forelimb biomechanics of nonavian theropod dinosaurs in predation" (pdf). Senckebergiana lethaea. 82 (1): 59–76.
  20. ^ Paul, Gregory S. (1988). Predatory Dinosaurs of the World. 113; note illustrations of Allosaurus on 310 and 311 as well; Madsen (1976) interpreted these bones as possible upper portions of the inner metatarsal.
  21. ^ a b Marsh, Othniel Charles (1878). "Notice of new dinosaurian reptiles". American Journal of Science and Arts. 15: 241–244.
  22. ^ von Huene, Friedrich (1926). "The carnivorous Saurischia in the Jura and Cretaceous formations, principally in Europe". Revista del Museo de La Plata. 29: 35–167.
  23. ^ Romer, Alfred S. (1956). Osteology of the Reptiles. Chicago: University of Chicago Press. ISBN 0-89464985-X.
  24. ^ Romer, Alfred S. (1966). Vertebrate Paleontology (Third ed.). Chicago: University of Chicago Press. ISBN 0-7167-1822-7.
  25. ^ Steel, R. (1970). "Part 14. Saurischia. Handbuch der Paläoherpetologie/Encyclopedia of Paleoherpetology". Gustav Fischer Verlag, Stuttgart: 1–87.
  26. ^ Walker, Alick D. (1964). "Triassic reptiles from the Elgin area: Ornithosuchus and the origin of carnosaurs". Philosophical Transactions of the Royal Society of London, Series B, Biological Sciences. 248 (744): 53–134. doi:10.1098/rstb.1964.0009.
  27. ^ a b Lambert, David (1983). "Allosaurids". A Field Guide to Dinosaurs. New York: Avon Books. pp. 80–81. ISBN 0-380-83519-3. {{cite book}}: Unknown parameter |coauthors= ignored (|author= suggested) (help)
  28. ^ a b Lambert, David (1990). "Allosaurids". The Dinosaur Data Book. New York: Avon Books. p. 130. ISBN 0-380-75896-3. {{cite book}}: Check |isbn= value: checksum (help); Unknown parameter |coauthors= ignored (|author= suggested) (help) Cite error: The named reference "DL90" was defined multiple times with different content (see the help page).
  29. ^ Paul, Gregory S. (1988). "The allosaur-tyrannosaur group", Predatory Dinosaurs of the World. 301–347.
  30. ^ Holtz, Thomas R., Jr. (1994). "The phylogenetic position of the Tyrannosauridae: Implications for theropod systematics". Journal of Paleontology. 68 (5): 1100–1117.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  31. ^ Leidy, Joseph (1870). "Remarks on Poicilopleuron valens, Clidastes intermedius, Leiodon proriger, Baptemys wyomingensis, and Emys stevensonianus". Proceedings of the Academy of Natural Sciences, Philadelphia. 22: 3–4.
  32. ^ Leidy, Joseph (1873). "Contribution to the extinct vertebrate fauna of the western territories". Report of the U.S. Geological Survey of the Territories I: 14–358.
  33. ^ Liddell & Scott (1980). Greek–English Lexicon, Abridged Edition. Oxford: Oxford University Press. ISBN 0-19-910207-4. OCLC 17396377 187441362 213803616 217157617 225305941 237142939 43379590 78588771. {{cite book}}: Check |oclc= value (help)
  34. ^ a b Marsh, Othniel Charles (1877). "Notice of new dinosaurian reptiles from the Jurassic formation". American Journal of Science and Arts. 14: 514–516.
  35. ^ Creisler, Ben (2003-07-07). "Dinosauria Translation and Pronunciation Guide A". Dinosauria On-Line. Retrieved 2007-09-11.
  36. ^ Marsh, Othniel Charles (1879). "Principal characters of American Jurassic dinosaurs. Part II". American Journal of Science, Series 3. 17: 86–92.
  37. ^ Cope, Edward Drinker (1878). "A new opisthocoelous dinosaur". American Naturalist. 12 (6): 406. doi:10.1086/272127.
  38. ^ Norell, Mark A. (1995). Discovering Dinosaurs in the American Museum of Natural History. New York: Knopf. pp. 112–113. ISBN 0-679-43386-4. {{cite book}}: Unknown parameter |coauthors= ignored (|author= suggested) (help)
  39. ^ Breithaupt, Brent H. (1999). "AMNH 5753: The world's first free-standing theropod skeleton". Journal of Vertebrate Paleontology. 19 (3, Suppl.): 33A. {{cite journal}}: Unknown parameter |coauthors= ignored (|author= suggested) (help)
  40. ^ Williston, Samuel Wendell (1878). "American Jurassic dinosaurs". Transactions of the Kansas Academy of Science. 6: 42–46.
  41. ^ Williston, Samuel Wendell (1901). "The dinosaurian genus Creosaurus, Marsh". American Journal of Science, series 4. 11 (11): 111–114.
  42. ^ a b Henderson, Donald M. (1998). "Skull and tooth morphology as indicators of niche partitioning in sympatric Morrison Formation theropods" (pdf). Gaia. 15: 219–266. ISSN 0871-5424.
  43. ^ Stokes, William J. (1945). "A new quarry for Jurassic dinosaurs". Science. 101 (2614): 115–117. doi:10.1126/science.101.2614.115-a. PMID 17799203.
  44. ^ Hunt, Adrian P (2006). "The taphonomy of the Cleveland-Lloyd Dinosaur Quarry, Upper Jurassic Morrison Formation, Utah: a re-evaluation". In Foster, John R.; and Lucas, Spencer G. (eds.) (ed.). Paleontology and Geology of the Upper Jurassic Morrison Formation. New Mexico Museum of Natural History and Science Bulletin, 36. Albuquerque, New Mexico: New Mexico Museum of Natural History and Science. pp. 57–65. {{cite book}}: |editor= has generic name (help); Unknown parameter |coauthors= ignored (|author= suggested) (help)CS1 maint: multiple names: editors list (link)
  45. ^ Loewen, Mark A. (2003). "Morphology, taxonomy, and stratigraphy of Allosaurus from the Upper Jurassic Morrison Formation". Journal of Vertebrate Paleontology. 23 (3, Suppl.): 72A. {{cite journal}}: Unknown parameter |coauthors= ignored (|author= suggested) (help)
  46. ^ a b Smith, David K. (1998). "A morphometric analysis of Allosaurus". Journal of Vertebrate Paleontology. 18 (1): 126–142.
  47. ^ a b Bybee, Paul J. (2006). "Sizing the Jurassic theropod dinosaur Allosaurus: Assessing growth strategy and evolution of ontogenetic scaling of limbs". Journal of Morphology. 267 (3): 347–359. doi:10.1002/jmor.10406. {{cite journal}}: Unknown parameter |coauthors= ignored (|author= suggested) (help)
  48. ^ a b Foster, John R. (2006). "Hindlimb allometry in the Late Jurassic theropod dinosaur Allosaurus, with comments on its abundance and distribution". In Foster, John R.; and Lucas, Spencer G. (eds.) (ed.). Paleontology and Geology of the Upper Jurassic Morrison Formation. New Mexico Museum of Natural History and Science Bulletin, 36. Albuquerque, New Mexico: New Mexico Museum of Natural History and Science. pp. 119–122. {{cite book}}: |editor= has generic name (help); Unknown parameter |coauthors= ignored (|author= suggested) (help)CS1 maint: multiple names: editors list (link)
  49. ^ a b Rayfield, Emily J. (2001). "Cranial design and function in a large theropod dinosaur". Nature. 409: 1033–1037. doi:10.1038/35059070. {{cite journal}}: Unknown parameter |coauthors= ignored (|author= suggested) (help)
  50. ^ a b Bakker, Robert T. (1998). "Brontosaur killers: Late Jurassic allosaurids as sabre-tooth cat analogues" (pdf). Gaia. 15: 145–158. ISSN 0871-5424. {{cite journal}}: Cite has empty unknown parameter: |coauthors= (help)
  51. ^ a b Rogers, Scott W. (1999). "Allosaurus, crocodiles, and birds: Evolutionary clues from spiral computed tomography of an endocast" (pdf). The Anatomical Record. 257 (5): 163–173. doi:10.1002/(SICI)1097-0185(19991015)257:5<162::AID-AR5>3.0.CO;2-W.
  52. ^ a b Bakker, Robert T. (1997). "Raptor Family values: Allosaur parents brought giant carcasses into their lair to feed their young". In Wolberg, Donald L.; Sump, Edmund; and Rosenberg, Gary D. (eds.) (ed.). Dinofest International, Proceedings of a Symposium Held at Arizona State University. Philadelphia: Academy of Natural Sciences. pp. 51–63. ISBN 0-935868-94-1. {{cite book}}: |editor= has generic name (help)CS1 maint: multiple names: editors list (link)
  53. ^ Chure, Daniel J. (1995). "A reassessment of the gigantic theropod Saurophagus maximus from the Morrison Formation (Upper Jurassic) of Oklahoma, USA". Sixth Symposium on Mesozoic Terrestrial Ecosystems and Biota, Short Papers. Beijing: China Ocean Press. pp. 103–106. ISBN 7-5027-3898-3. {{cite book}}: Unknown parameter |editors= ignored (|editor= suggested) (help)
  54. ^ Pérez-Moreno, B.P. (1999). "On the presence of Allosaurus fragilis (Theropoda: Carnosauria) in the Upper Jurassic of Portugal: First evidence of an intercontinental dinosaur species" (pdf). Journal of the Geological Society. 156 (3): 449–452. doi:10.1144/gsjgs.156.3.0449. {{cite journal}}: Unknown parameter |coauthors= ignored (|author= suggested) (help)
  55. ^ a b Breithaupt, Brent (1996). "The discovery of a nearly complete Allosaurus from the Jurassic Morrison Formation, eastern Bighorn Basin, Wyoming". Forty-Seventh Annual Field Conference Guidebook. Casper, Wyoming: Wyoming Geological Association. pp. 309–313. OCLC 36004754. {{cite book}}: Unknown parameter |editors= ignored (|editor= suggested) (help)
  56. ^ a b "Howe Dinosaur Quarry – Wyoming's Jurassic Treasure". GeoScience Adventures. 2007-07-24. Retrieved 2007-09-27.
  57. ^ Piotrowska, Anna (2001.12.09). "Tropami dinozaurów". Newsweek (Polish edition) (in Polish): 68–70. {{cite journal}}: Check date values in: |date= (help)
  58. ^ a b Breithaupt, Brent H. "The case of "Big Al" the Allosaurus: a study in paleodetective partnerships". Retrieved 2007-10-03.
  59. ^ a b Hanna, Rebecca R. (2002). "Multiple injury and infection in a sub-adult theropod dinosaur (Allosaurus fragilis) with comparisons to allosaur pathology in the Cleveland-Lloyd dinosaur quarry collection". Journal of Vertebrate Paleontology. 22 (1): 76–90. doi:10.1671/0272-4634(2002)022[0076:MIAIIA]2.0.CO;2.
  60. ^ a b Mateus, Octávio (2006). "The large theropod fauna of the Lourinha Formation (Portugal) and its similarity to that of the Morrison Formation, with a description of a new species of Allosaurus". In Foster, John R.; and Lucas, Spencer G. (eds.) (ed.). Paleontology and Geology of the Upper Jurassic Morrison Formation. New Mexico Museum of Natural History and Science Bulletin, 36. Albuquerque, New Mexico: New Mexico Museum of Natural History and Science. pp. 123–129. {{cite book}}: |editor= has generic name (help); Unknown parameter |coauthors= ignored (|author= suggested) (help)CS1 maint: multiple names: editors list (link)
  61. ^ a b c Lessem, Don (1993). "Allosaurus". The Dinosaur Society's Dinosaur Encyclopedia. Random House. pp. 19–20. ISBN 0-679-41770-2. OCLC 30361459. {{cite book}}: Unknown parameter |coauthors= ignored (|author= suggested) (help)
  62. ^ Smith, David K. (1996). "A discriminant analysis of Allosaurus population using quarries as the operational units". Museum of Northern Arizona Bulletin. 60: 69–72.
  63. ^ Smith, David K. (1999). "Patterns of size-related variation within Allosaurus". Journal of Vertebrate Paleontology. 19 (2): 402–403.
  64. ^ Malafaia, Elisabete (2007). "Nuevos restos de Allosaurus fragilis (Theropoda: Carnosauria) del yacimiento de Andrés (Jurásico Superior; centro-oeste de Portugal)" (pdf). Cantera Paleontológica (in Spanish with English abstract): 255–271. {{cite journal}}: Unknown parameter |coauthors= ignored (|author= suggested) (help)CS1 maint: unrecognized language (link)
  65. ^ Janensch, Werner (1925). "Die Coelurosaurier und Theropoden der Tendaguru-Schichten Deutsch-Ostafrikas". Palaeontographica, Supplement 7 (in German). 1: 1–99.
  66. ^ Rauhut, Oliver W.M. (2005). "Post-cranial remains of 'coelurosaurs' (Dinosauria, Theropoda) from the Late Jurassic of Tanzania". Geological Magazine. 142 (1): 97–107. doi:10.1017/S0016756804000330.
  67. ^ Marsh, Othniel Charles (1884). "Principal characters of American Jurassic dinosaurs. Part VIII". American Journal of Science, Series 3. 27: 329–340.
  68. ^ Madsen, James H. (2000). Ceratosaurus (Dinosauria, Theropoda), a Revised Osteology. Miscellaneous Publication, 00-2. Utah Geological Survey. {{cite book}}: Unknown parameter |coauthors= ignored (|author= suggested) (help)
  69. ^ Molnar, Ralph E. (1981). "An allosaurid theropod dinosaur from the Early Cretaceous of Victoria, Australia". Alcheringa. 5: 141–146. doi:10.1080/03115518108565427. {{cite journal}}: Unknown parameter |coauthors= ignored (|author= suggested) (help)
  70. ^ Riabinin, Anatoly Nikolaenvich (1914). "Zamtka o dinozavry ise Zabaykalya". Trudy Geologichyeskago Muszeyah Imeni Petra Velikago Imperatorskoy Academiy Nauk (in Russian). 8 (5): 133–140.
  71. ^ Foster, John R. (2003). Paleoecological Analysis of the Vertebrate Fauna of the Morrison Formation (Upper Jurassic), Rocky Mountain Region, U.S.A. New Mexico Museum of Natural History and Science Bulletin, 23. Albuquerque, New Mexico: New Mexico Museum of Natural History and Science. p. 29.
  72. ^ Russell, Dale A. (1989). An Odyssey in Time: Dinosaurs of North America. Minocqua, Wisconsin: NorthWord Press. pp. 175–176. ISBN 1-55971-038-1.
  73. ^ Carpenter, Kenneth (2006). "Biggest of the big: a critical re-evaluation of the mega-sauropod Amphicoelias fragillimus". Paleontology and Geology of the Upper Jurassic Morrison Formation (pdf). New Mexico Museum of Natural History and Science Bulletin, 36. Albuquerque, New Mexico: New Mexico Museum of Natural History and Science. pp. 131–138. {{cite book}}: Unknown parameter |editors= ignored (|editor= suggested) (help)
  74. ^ Chure, Daniel J. (2006). "The fauna and flora of the Morrison Formation: 2006". In Foster, John R.; and Lucas, Spencer G. (eds.) (ed.). Paleontology and Geology of the Upper Jurassic Morrison Formation. New Mexico Museum of Natural History and Science Bulletin, 36. Albuquerque, New Mexico: New Mexico Museum of Natural History and Science. pp. 233–248. {{cite book}}: |editor= has generic name (help); Unknown parameter |coauthors= ignored (|author= suggested) (help)CS1 maint: multiple names: editors list (link)
  75. ^ a b Mateus, Octávio (2006). "Jurassic dinosaurs from the Morrison Formation (USA), the Lourinhã and Alcobaça Formations (Portugal), and the Tendaguru Beds (Tanzania): A comparison". In Foster, John R.; and Lucas, Spencer G. (eds.) (ed.). Paleontology and Geology of the Upper Jurassic Morrison Formation. New Mexico Museum of Natural History and Science Bulletin, 36. Albuquerque, New Mexico: New Mexico Museum of Natural History and Science. pp. 223–231. {{cite book}}: |editor= has generic name (help)CS1 maint: multiple names: editors list (link)
  76. ^ a b Bakker, Robert T. (2004). "Dinosaur crime scene investigations: theropod behavior at Como Bluff, Wyoming, and the evolution of birdness". In Currie, Philip J.; Koppelhus, Eva B.; Shugar, Martin A.; and Wright, Joanna L. (eds.) (ed.). Feathered Dragons: Studies on the Transition from Dinosaurs to Birds. Bloomington and Indianapolis: Indiana University Press. pp. 301–342. ISBN 0-253-34373-9. {{cite book}}: |editor= has generic name (help); Unknown parameter |coauthors= ignored (|author= suggested) (help)CS1 maint: multiple names: editors list (link)
  77. ^ Chure, Daniel J. (2000). "Prey bone utilization by predatory dinosaurs in the Late Jurassic of North America, with comments on prey bone use by dinosaurs throughout the Mesozoic" (pdf). Gaia. 15: 227–232. ISSN 0871-5424. {{cite journal}}: Unknown parameter |coauthors= ignored (|author= suggested) (help)
  78. ^ Lee, Andrew H. (2008). "Sexual maturity in growing dinosaurs does not fit reptilian growth models". Proceedings of the National Academy of Sciences. 105 (2): 582–587. doi:10.1073/pnas.0708903105. PMID 18195356. {{cite journal}}: Unknown parameter |coauthors= ignored (|author= suggested) (help)
  79. ^ Loewen, Mark A. (2002). "Ontogenetic changes in hindlimb musculature and function in the Late Jurassic theropod Allosaurus". Journal of Vertebrate Paleontology. 22 (3, Suppl.): 80A. {{cite journal}}: Unknown parameter |coauthors= ignored (|author= suggested) (help)
  80. ^ Fastovsky, David E.; and Smith, Joshua B. (2004). "Dinosaur Paleoecology", in The Dinosauria (2nd). 614–626.
  81. ^ Kenneth, Carpenter (2005). "Evidence for predator-prey relationships: Examples for Allosaurus and Stegosaurus". In Carpenter, Kenneth (ed.) (ed.). The Carnivorous Dinosaurs (pdf). Bloomington and Indianapolis: Indiana University Press. pp. 325–350. ISBN 0-253-34539-1. {{cite book}}: |editor= has generic name (help); Unknown parameter |coauthors= ignored (|author= suggested) (help)
  82. ^ Frazzetta, T.H. (2002). "Prey attack by a large theropod dinosaur". Nature. 416: 387–388. doi:10.1038/416387a. {{cite journal}}: Unknown parameter |coauthors= ignored (|author= suggested) (help)
  83. ^ Rayfield, Emily J. (2002). "Prey attack by a large theropod dinosaur: Response to Frazzetta and Kardong, 2002". Nature. 416: 388. doi:10.1038/416388a. {{cite journal}}: Unknown parameter |coauthors= ignored (|author= suggested) (help)
  84. ^ Stevens, Kent A. (2006). "Binocular vision in theropod dinosaurs". Journal of Vertebrate Paleontology. 26 (2): 321–330. doi:10.1671/0272-4634(2006)26[321:BVITD]2.0.CO;2.
  85. ^ "Evolve: Eyes". History channel Evolve. {{cite episode}}: External link in |transcripturl= (help); Unknown parameter |transcripturl= ignored (|transcript-url= suggested) (help)
  86. ^ Christiansen, Per (1998). "Strength indicator values of theropod long bones, with comments on limb proportions and cursorial potential" (pdf). Gaia. 15: 241–255. ISSN 0871-5424.
  87. ^ Tanke, Darren H. (1998). "Head-biting behavior in theropod dinosaurs: Paleopathological evidence" (pdf). Gaia (15): 167–184. ISSN 0871-5424. {{cite journal}}: Unknown parameter |coauthors= ignored (|author= suggested) (help)
  88. ^ Currie, Philip J. (1999). "Theropods". In Farlow, James; and Brett-Surman, M.K. (eds.) (ed.). The Complete Dinosaur. Indiana: Indiana University Press. p. 228. ISBN 0253213134. {{cite book}}: |editor= has generic name (help)CS1 maint: multiple names: editors list (link)
  89. ^ Roach, Brian T. (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. {{cite journal}}: Unknown parameter |coauthors= ignored (|author= suggested) (help)
  90. ^ Goodchild Drake, Brandon (2004). "A new specimen of Allosaurus from north-central Wyoming". Journal of Vertebrate Paleontology. 24 (3, Suppl.): 65A.
  91. ^ "Utah Symbols – State Fossil". State of Utah. Retrieved 2007-09-30.
  92. ^ Glut, Donald F.; Brett-Surman, Michael K. (1997). "Dinosaurs and the media", in Farlow, James; and Brett-Surman, Michael K. (eds.): The Complete Dinosaur. Bloomington and Indianapolis: Indiana University Press, 675–706. ISBN 0-253-33349-0.
  93. ^ Return to the Valley, a documentary on the Region 1 Valley of Gwangi DVD.
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