Tyrannosaurus

Skin and possible feathers

Head model showing "traditional" naked skin and lipless jaws, Natural History Museum of Vienna

While there is no direct evidence for Tyrannosaurus rex having had feathers, many scientists now consider it likely that T. rex had feathers on at least parts of its body,^[31] due to their presence in related species. Mark Norell of the American Museum of Natural History summarized the balance of evidence by stating that: "we have as much evidence that T. rex was feathered, at least during some stage of its life, as we do that australopithecines like Lucy had hair."^[32]

The first evidence for feathers in tyrannosauroids came from the small species Dilong paradoxus, found in the Yixian Formation of China, and reported in 2004. As with many other coelurosaurian theropods discovered in the Yixian, the fossil skeleton was preserved with a coat of filamentous structures which are commonly recognized as the precursors of feathers.^[33] Because all known skin impressions from larger tyrannosauroids known at the time showed evidence of scales, the researchers who studied Dilong speculated that feathers may correlate negatively with body size—that juveniles may have been feathered, then shed the feathers and expressed only scales as the animal became larger and no longer needed insulation to stay warm.^[33] Subsequent discoveries showed that even some large tyrannosauroids had feathers covering much of their bodies, casting doubt on the hypothesis that they were a size-related feature.^[34]

Full-size model in Poland, depicting Tyrannosaurus with both feathers and scales, as well as lipped jaws

While skin impressions from a Tyrannosaurus rex specimen nicknamed "Wyrex" (BHI 6230) discovered in Montana in 2002,^[35] as well as some other giant tyrannosauroid specimens, show at least small patches of mosaic scales,^[36] others, such as Yutyrannus huali (which was up to 9 meters (30 ft) long and weighed about 1,400 kilograms (3,100 lb)), preserve feathers on various sections of the body, strongly suggesting that its whole body was covered in feathers.^[34] It is possible that the extent and nature of feather covering in tyrannosauroids may have changed over time in response to body size, a warmer climate, or other factors.^[34] In 2017, based on skin impressions found on the tail, ilium and neck of the "Wyrex" (BHI 6230) specimen and other closely related tyrannosaurids, it was suggested that large-bodied tyrannosaurids were scaly and, if partly feathered, these were limited to the dorsum.^[37]

A study in 2016 proposed that large theropods like Tyrannosaurus had teeth covered in lips like extant lizards instead of bare teeth like crocodilians. This was based on the presence of enamel, which according to the study needs to remain hydrated, an issue not faced by aquatic animals like crocodilians or toothless animals like birds.^[38][39]

Based on comparisons of bone texture of Daspletosaurus with extant crocodilians, a detailed study in 2017 by Thomas D. Carr et al. found that tyrannosaurs had large, flat scales on their snouts. At the center of these scales were small keratinised patches. In crocodilians, such patches cover bundles of sensory neurons that can detect mechanical, thermal and chemical stimuli.^[40][41] They proposed that tyrannosaurs probably also had bundles of sensory neurons under their facial scales and may have used them to identify objects, measure the temperature of their nests and gently pick-up eggs and hatchlings.^[42] Although the study did not explicitly discuss the evidence for or against lips, many major news outlets considered it as evidence against tyrannosaurs having lips. Comparisons with crocodilian facial tissue and Thomas D. Carr's personal interpretation of the findings were cited as support for the conclusion that tyrannosaurs did not have lips.^[43][44]

Earliest finds

Type specimen of Dynamosaurus imperiosus

Teeth from what is now documented as a Tyrannosaurus rex were found in 1874 by Arthur Lakes near Golden, Colorado. In the early 1890s, John Bell Hatcher collected postcranial elements in eastern Wyoming. The fossils were believed to be from a large species of Ornithomimus (O. grandis) but are now considered Tyrannosaurus rex remains. Vertebral fragments found by Edward Drinker Cope in western South Dakota in 1892 and assigned to Manospondylus gigas have also been recognized as belonging to Tyrannosaurus rex.^[48]

Barnum Brown, assistant curator of the American Museum of Natural History, found the first partial skeleton of Tyrannosaurus rex in eastern Wyoming in 1900. H. F. Osborn originally named this skeleton Dynamosaurus imperiosus in a paper in 1905. Brown found another partial skeleton in the Hell Creek Formation in Montana in 1902. Osborn used this holotype to describe Tyrannosaurus rex in the same paper in which D. imperiosus was described.^[47] In 1906, Osborn recognized the two as synonyms, and acted as first revisor by selecting Tyrannosaurus as the valid name.^[49] The original Dynamosaurus material resides in the collections of the Natural History Museum, London.^[50]

In total, Brown found five Tyrannosaurus partial skeletons. In 1941, Brown's 1902 find was sold to the Carnegie Museum of Natural History in Pittsburgh, Pennsylvania. Brown's fourth and largest find, also from Hell Creek, is on display in the American Museum of Natural History in New York.^[51]

Manospondylus

Illustration of the type specimen (AMNH 3982) of Manospondylus gigas

The first named fossil specimen which can be attributed to Tyrannosaurus rex consists of two partial vertebrae (one of which has been lost) found by Edward Drinker Cope in 1892. Cope believed that they belonged to an "agathaumid" (ceratopsid) dinosaur, and named them Manospondylus gigas, meaning "giant porous vertebra" in reference to the numerous openings for blood vessels he found in the bone.^[48] The M. gigas remains were later identified by Hatcher as those of a theropod rather than a ceratopsid,^[52] and H. F. Osborn recognized the similarity between M. gigas and Tyrannosaurus rex as early as 1917. Owing to the fragmentary nature of the Manospondylus vertebrae, Osborn did not synonymize the two genera.^[53]

In June 2000, the Black Hills Institute located the type locality of M. gigas in South Dakota and unearthed more tyrannosaur bones there. These were judged to represent further remains of the same individual, and to be identical to those of Tyrannosaurus rex.^[54] According to the rules of the International Code of Zoological Nomenclature (ICZN), the system that governs the scientific naming of animals, Manospondylus gigas should therefore have priority over Tyrannosaurus rex, because it was named first. The Fourth Edition of the ICZN, which took effect on January 1, 2000, states that "the prevailing usage must be maintained" when "the senior synonym or homonym has not been used as a valid name after 1899" and "the junior synonym or homonym has been used for a particular taxon, as its presumed valid name, in at least 25 works, published by at least 10 authors in the immediately preceding 50 years ..."^[55] Tyrannosaurus rex may qualify as the valid name under these conditions and would most likely be considered a nomen protectum ("protected name") under the ICZN if it is ever formally published on, which it has not yet been. Manospondylus gigas could then be deemed a nomen oblitum ("forgotten name").^[56]

Notable specimens

Sue specimen, Field Museum of Natural History, Chicago

Sue Hendrickson, amateur paleontologist, discovered the most complete (approximately 85%) and the largest Tyrannosaurus fossil skeleton known in the Hell Creek Formation near Faith, South Dakota, on August 12, 1990. This Tyrannosaurus, nicknamed Sue in her honor, was the object of a legal battle over its ownership. In 1997 this was settled in favor of Maurice Williams, the original land owner. The fossil collection was purchased by the Field Museum of Natural History at auction for $7.6 million, making it the most expensive dinosaur skeleton to date. From 1998 to 1999 Field Museum of Natural History preparators spent over 25,000 man-hours taking the rock off each of the bones.^[57] The bones were then shipped off to New Jersey where the mount was made. The finished mount was then taken apart, and along with the bones, shipped back to Chicago for the final assembly. The mounted skeleton opened to the public on May 17, 2000 in the great hall (Stanley Field Hall) at the Field Museum of Natural History. A study of this specimen's fossilized bones showed that Sue reached full size at age 19 and died at age 28, the longest any tyrannosaur is known to have lived.^[58] Early speculation that Sue may have died from a bite to the back of the head was not confirmed. Though subsequent study showed many pathologies in the skeleton, no bite marks were found.^[22][59] Damage to the back of the skull may have been caused by post-mortem trampling. Recent speculation indicates that Sue may have died of starvation after contracting a parasitic infection from eating diseased meat; the resulting infection would have caused inflammation in the throat, ultimately leading Sue to starve because she could no longer swallow food. This hypothesis is substantiated by smooth-edged holes in her skull which are similar to those caused in modern-day birds that contract the same parasite.^[60]

Skeleton of Bucky and cast of Stan, at the Children's Museum of Indianapolis

Another Tyrannosaurus, nicknamed Stan, in honor of amateur paleontologist Stan Sacrison, was found in the Hell Creek Formation near Buffalo, South Dakota, in the spring of 1987. It was not collected until 1992, as it was mistakenly thought to be a Triceratops skeleton. Stan is 63% complete and is on display in the Black Hills Institute of Geological Research in Hill City, South Dakota, after an extensive world tour during 1995 and 1996.^[35] This tyrannosaur, too, was found to have many bone pathologies, including broken and healed ribs, a broken (and healed) neck and a spectacular hole in the back of its head, about the size of a Tyrannosaurus tooth.^[61]

In the summer of 2000, Jack Horner discovered five Tyrannosaurus skeletons near the Fort Peck Reservoir in Montana. One of the specimens was reported to be perhaps the largest Tyrannosaurus ever found.^[62]

The specimens "Sue", AMNH 5027, "Stan", and "Jane", to scale with a human.

In 2001, a 50% complete skeleton of a juvenile Tyrannosaurus was discovered in the Hell Creek Formation in Montana, by a crew from the Burpee Museum of Natural History of Rockford, Illinois. Dubbed Jane, the find was initially considered the first known skeleton of the pygmy tyrannosaurid Nanotyrannus but subsequent research has revealed that it is more likely a juvenile Tyrannosaurus.^[63] It is the most complete and best preserved juvenile example known to date. Jane has been examined by Jack Horner, Pete Larson, Robert Bakker, Greg Erickson, and several other renowned paleontologists, because of the uniqueness of her age. Jane is currently on exhibit at the Burpee Museum of Natural History in Rockford, Illinois.^[64][65]

In a press release in 2006, Montana State University revealed that it possessed the largest Tyrannosaurus skull yet discovered. Discovered in the 1960s and only recently reconstructed, the skull measured 59 inches (150 cm) long compared to the 55.4 inches (141 cm) of Sue's skull, a difference of 6.5%.^[66]

Life history

A graph showing the hypothesized growth curve, body mass versus age (drawn in black, with other tyrannosaurids for comparison). Based on Erickson et al. 2004

The identification of several specimens as juvenile Tyrannosaurus rex has allowed scientists to document ontogenetic changes in the species, estimate the lifespan, and determine how quickly the animals would have grown. The smallest known individual (LACM 28471, the "Jordan theropod") is estimated to have weighed only 30 kg (66 lb), while the largest, such as FMNH PR2081 (Sue) most likely weighed about 5,650 kg (12,460 lb). Histologic analysis of Tyrannosaurus rex bones showed LACM 28471 had aged only 2 years when it died, while Sue was 28 years old, an age which may have been close to the maximum for the species.^[15]

Histology has also allowed the age of other specimens to be determined. Growth curves can be developed when the ages of different specimens are plotted on a graph along with their mass. A Tyrannosaurus rex growth curve is S-shaped, with juveniles remaining under 1,800 kg (4,000 lb) until approximately 14 years of age, when body size began to increase dramatically. During this rapid growth phase, a young Tyrannosaurus rex would gain an average of 600 kg (1,300 lb) a year for the next four years. At 18 years of age, the curve plateaus again, indicating that growth slowed dramatically. For example, only 600 kg (1,300 lb) separated the 28-year-old Sue from a 22-year-old Canadian specimen (RTMP 81.12.1).^[15] A 2004 histological study performed by different workers corroborates these results, finding that rapid growth began to slow at around 16 years of age.^[88]

11-year-old juvenile (Jane) specimen, with adult in the background, Burpee Museum of Natural History

A study by Hutchinson et al. in 2011 corroborated the previous estimation methods in general, but their estimation of peak growth rates is significantly higher; it found that the "maximum growth rates for T. rex during the exponential stage are 1790 kg/year".^[4] Although these results were much higher than previous estimations, the authors noted that these results significantly lowered the great difference between its actual growth rate and the one which would be expected of an animal of its size.^[4] The sudden change in growth rate at the end of the growth spurt may indicate physical maturity, a hypothesis which is supported by the discovery of medullary tissue in the femur of a 16 to 20-year-old Tyrannosaurus rex from Montana (MOR 1125, also known as B-rex). Medullary tissue is found only in female birds during ovulation, indicating that B-rex was of reproductive age.^[89] Further study indicates an age of 18 for this specimen.^[90] In 2016, it was finally confirmed by Mary Higby Schweitzer and Lindsay Zanno et al that the soft tissue within the femur of MOR 1125 was medullary tissue. This also confirmed the identity of the specimen as a female. The discovery of medullary bone tissue within Tyrannosaurus may prove valuable in determining the sex of other dinosaur species in future examinations, as the chemical makeup of medullary tissue is unmistakable.^[91] Other tyrannosaurids exhibit extremely similar growth curves, although with lower growth rates corresponding to their lower adult sizes.^[92]

Over half of the known Tyrannosaurus rex specimens appear to have died within six years of reaching sexual maturity, a pattern which is also seen in other tyrannosaurs and in some large, long-lived birds and mammals today. These species are characterized by high infant mortality rates, followed by relatively low mortality among juveniles. Mortality increases again following sexual maturity, partly due to the stresses of reproduction. One study suggests that the rarity of juvenile Tyrannosaurus rex fossils is due in part to low juvenile mortality rates; the animals were not dying in large numbers at these ages, and so were not often fossilized. This rarity may also be due to the incompleteness of the fossil record or to the bias of fossil collectors towards larger, more spectacular specimens.^[92] In a 2013 lecture, Thomas Holtz Jr. suggested that dinosaurs "lived fast and died young" because they reproduced quickly whereas mammals have long life spans because they take longer to reproduce.^[93] Gregory S. Paul also writes that Tyrannosaurus reproduced quickly and died young, but attributes their short life spans to the dangerous lives they lived.^[94]

Sexual dimorphism

Skeleton casts mounted in a mating position, Jurassic Museum of Asturias

As the number of known specimens increased, scientists began to analyze the variation between individuals and discovered what appeared to be two distinct body types, or morphs, similar to some other theropod species. As one of these morphs was more solidly built, it was termed the 'robust' morph while the other was termed 'gracile'. Several morphological differences associated with the two morphs were used to analyze sexual dimorphism in Tyrannosaurus rex, with the 'robust' morph usually suggested to be female. For example, the pelvis of several 'robust' specimens seemed to be wider, perhaps to allow the passage of eggs.^[95] It was also thought that the 'robust' morphology correlated with a reduced chevron on the first tail vertebra, also ostensibly to allow eggs to pass out of the reproductive tract, as had been erroneously reported for crocodiles.^[96]

In recent years, evidence for sexual dimorphism has been weakened. A 2005 study reported that previous claims of sexual dimorphism in crocodile chevron anatomy were in error, casting doubt on the existence of similar dimorphism between Tyrannosaurus rex sexes.^[97] A full-sized chevron was discovered on the first tail vertebra of Sue, an extremely robust individual, indicating that this feature could not be used to differentiate the two morphs anyway. As Tyrannosaurus rex specimens have been found from Saskatchewan to New Mexico, differences between individuals may be indicative of geographic variation rather than sexual dimorphism. The differences could also be age-related, with 'robust' individuals being older animals.^[22]

Only a single Tyrannosaurus rex specimen has been conclusively shown to belong to a specific sex. Examination of B-rex demonstrated the preservation of soft tissue within several bones. Some of this tissue has been identified as a medullary tissue, a specialized tissue grown only in modern birds as a source of calcium for the production of eggshell during ovulation. As only female birds lay eggs, medullary tissue is only found naturally in females, although males are capable of producing it when injected with female reproductive hormones like estrogen. This strongly suggests that B-rex was female, and that she died during ovulation.^[89] Recent research has shown that medullary tissue is never found in crocodiles, which are thought to be the closest living relatives of dinosaurs, aside from birds. The shared presence of medullary tissue in birds and theropod dinosaurs is further evidence of the close evolutionary relationship between the two.^[98]

Posture

Outdated reconstruction (by Charles R. Knight), showing upright pose

Modern representations in museums, art, and film show Tyrannosaurus rex with its body approximately parallel to the ground and tail extended behind the body to balance the head.^[99]

Like many bipedal dinosaurs, Tyrannosaurus rex was historically depicted as a 'living tripod', with the body at 45 degrees or less from the vertical and the tail dragging along the ground, similar to a kangaroo. This concept dates from Joseph Leidy's 1865 reconstruction of Hadrosaurus, the first to depict a dinosaur in a bipedal posture.^[100] In 1915, convinced that the creature stood upright, Henry Fairfield Osborn, former president of the American Museum of Natural History, further reinforced the notion in unveiling the first complete Tyrannosaurus rex skeleton arranged this way. It stood in an upright pose for 77 years, until it was dismantled in 1992.^[101]

By 1970, scientists realized this pose was incorrect and could not have been maintained by a living animal, as it would have resulted in the dislocation or weakening of several joints, including the hips and the articulation between the head and the spinal column.^[102] The inaccurate AMNH mount inspired similar depictions in many films and paintings (such as Rudolph Zallinger's famous mural The Age of Reptiles in Yale University's Peabody Museum of Natural History)^[103] until the 1990s, when films such as Jurassic Park introduced a more accurate posture to the general public.^[104]

Arms

The forelimbs might have been used to help T. rex rise from a resting pose, as seen in this cast (Bucky specimen)

When Tyrannosaurus rex was first discovered, the humerus was the only element of the forelimb known.^[47] For the initial mounted skeleton as seen by the public in 1915, Osborn substituted longer, three-fingered forelimbs like those of Allosaurus.^[53] A year earlier, Lawrence Lambe described the short, two-fingered forelimbs of the closely related Gorgosaurus.^[105] This strongly suggested that Tyrannosaurus rex had similar forelimbs, but this hypothesis was not confirmed until the first complete Tyrannosaurus rex forelimbs were identified in 1989, belonging to MOR 555 (the "Wankel rex").^[51] The remains of Sue also include complete forelimbs.^[22] Tyrannosaurus rex arms are very small relative to overall body size, measuring only 1 meter (3.3 ft) long, and some scholars have labelled them as vestigial. The bones show large areas for muscle attachment, indicating considerable strength. This was recognized as early as 1906 by Osborn, who speculated that the forelimbs may have been used to grasp a mate during copulation.^[49] It has also been suggested that the forelimbs were used to assist the animal in rising from a prone position.^[102]

Diagram illustrating arm anatomy

Another possibility is that the forelimbs held struggling prey while it was killed by the tyrannosaur's enormous jaws. This hypothesis may be supported by biomechanical analysis. Tyrannosaurus rex forelimb bones exhibit extremely thick cortical bone, which has been interpreted as evidence that they were developed to withstand heavy loads. The biceps brachii muscle of an adult Tyrannosaurus rex was capable of lifting 199 kilograms (439 lb) by itself; other muscles such as the brachialis would work along with the biceps to make elbow flexion even more powerful. The M. biceps muscle of T. rex was 3.5 times as powerful as the human equivalent. A Tyrannosaurus rex forearm had a limited range of motion, with the shoulder and elbow joints allowing only 40 and 45 degrees of motion, respectively. In contrast, the same two joints in Deinonychus allow up to 88 and 130 degrees of motion, respectively, while a human arm can rotate 360 degrees at the shoulder and move through 165 degrees at the elbow. The heavy build of the arm bones, strength of the muscles, and limited range of motion may indicate a system evolved to hold fast despite the stresses of a struggling prey animal. In the first detailed scientific description of Tyrannosaurus forelimbs, paleontologists Kenneth Carpenter and Matt Smith dismissed notions that the forelimbs were useless or that Tyrannosaurus rex was an obligate scavenger.^[106]

According to paleontologist Steven Stanley from the University of Hawaii, the roughly 1 meter long arms of a Tyrannosaurus rex were used for slashing prey, especially by juvenile dinosaurs, as their arms grow slower in proportion to their bodies and a younger Tyrannosaurus rex would have proportionally much longer arms than an adult one.^[107]

Soft tissue

In the March 2005 issue of Science, Mary Higby Schweitzer of North Carolina State University and colleagues announced the recovery of soft tissue from the marrow cavity of a fossilized leg bone from a Tyrannosaurus rex. The bone had been intentionally, though reluctantly, broken for shipping and then not preserved in the normal manner, specifically because Schweitzer was hoping to test it for soft tissue.^[108] Designated as the Museum of the Rockies specimen 1125, or MOR 1125, the dinosaur was previously excavated from the Hell Creek Formation. Flexible, bifurcating blood vessels and fibrous but elastic bone matrix tissue were recognized. In addition, microstructures resembling blood cells were found inside the matrix and vessels. The structures bear resemblance to ostrich blood cells and vessels. Whether an unknown process, distinct from normal fossilization, preserved the material, or the material is original, the researchers do not know, and they are careful not to make any claims about preservation.^[109] If it is found to be original material, any surviving proteins may be used as a means of indirectly guessing some of the DNA content of the dinosaurs involved, because each protein is typically created by a specific gene. The absence of previous finds may be the result of people assuming preserved tissue was impossible, therefore not looking. Since the first, two more tyrannosaurs and a hadrosaur have also been found to have such tissue-like structures.^[108] Research on some of the tissues involved has suggested that birds are closer relatives to tyrannosaurs than other modern animals.^[110]

T. rex femur (MOR 1125) from which demineralized matrix and peptides (insets) were obtained

In studies reported in Science in April 2007, Asara and colleagues concluded that seven traces of collagen proteins detected in purified Tyrannosaurus rex bone most closely match those reported in chickens, followed by frogs and newts. The discovery of proteins from a creature tens of millions of years old, along with similar traces the team found in a mastodon bone at least 160,000 years old, upends the conventional view of fossils and may shift paleontologists' focus from bone hunting to biochemistry. Until these finds, most scientists presumed that fossilization replaced all living tissue with inert minerals. Paleontologist Hans Larsson of McGill University in Montreal, who was not part of the studies, called the finds "a milestone", and suggested that dinosaurs could "enter the field of molecular biology and really slingshot paleontology into the modern world".^[111]

The presumed soft tissue was called into question by Thomas Kaye of the University of Washington and his co-authors in 2008. They contend that what was really inside the tyrannosaur bone was slimy biofilm created by bacteria that coated the voids once occupied by blood vessels and cells.^[112] The researchers found that what previously had been identified as remnants of blood cells, because of the presence of iron, were actually framboids, microscopic mineral spheres bearing iron. They found similar spheres in a variety of other fossils from various periods, including an ammonite. In the ammonite they found the spheres in a place where the iron they contain could not have had any relationship to the presence of blood.^[113] Schweitzer has strongly criticized Kaye's claims and argues that there is no reported evidence that biofilms can produce branching, hollow tubes like those noted in her study.^[114] San Antonio, Schweitzer and colleagues published an analysis in 2011 of what parts of the collagen had been recovered, finding that it was the inner parts of the collagen coil that had been preserved, as would have been expected from a long period of protein degradation.^[115] Other research challenges the identification of soft tissue as biofilm and confirms finding "branching, vessel-like structures" from within fossilized bone.^[116]

Thermoregulation

Restoration showing partial feathering

As of 2014, it is not clear if Tyrannosaurus was endothermic (warm-blooded). Tyrannosaurus, like most dinosaurs, was long thought to have an ectothermic ("cold-blooded") reptilian metabolism. The idea of dinosaur ectothermy was challenged by scientists like Robert T. Bakker and John Ostrom in the early years of the "Dinosaur Renaissance", beginning in the late 1960s.^[117][118] Tyrannosaurus rex itself was claimed to have been endothermic ("warm-blooded"), implying a very active lifestyle.^[13] Since then, several paleontologists have sought to determine the ability of Tyrannosaurus to regulate its body temperature. Histological evidence of high growth rates in young Tyrannosaurus rex, comparable to those of mammals and birds, may support the hypothesis of a high metabolism. Growth curves indicate that, as in mammals and birds, Tyrannosaurus rex growth was limited mostly to immature animals, rather than the indeterminate growth seen in most other vertebrates.^[88]

Oxygen isotope ratios in fossilized bone are sometimes used to determine the temperature at which the bone was deposited, as the ratio between certain isotopes correlates with temperature. In one specimen, the isotope ratios in bones from different parts of the body indicated a temperature difference of no more than 4 to 5 °C (7 to 9 °F) between the vertebrae of the torso and the tibia of the lower leg. This small temperature range between the body core and the extremities was claimed by paleontologist Reese Barrick and geochemist William Showers to indicate that Tyrannosaurus rex maintained a constant internal body temperature (homeothermy) and that it enjoyed a metabolism somewhere between ectothermic reptiles and endothermic mammals.^[119] Other scientists have pointed out that the ratio of oxygen isotopes in the fossils today does not necessarily represent the same ratio in the distant past, and may have been altered during or after fossilization (diagenesis).^[120] Barrick and Showers have defended their conclusions in subsequent papers, finding similar results in another theropod dinosaur from a different continent and tens of millions of years earlier in time (Giganotosaurus).^[121] Ornithischian dinosaurs also showed evidence of homeothermy, while varanid lizards from the same formation did not.^[122] Even if Tyrannosaurus rex does exhibit evidence of homeothermy, it does not necessarily mean that it was endothermic. Such thermoregulation may also be explained by gigantothermy, as in some living sea turtles.^{[123][124][125]}

Footprints

Probable footprint from New Mexico

Two isolated fossilized footprints have been tentatively assigned to Tyrannosaurus rex. The first was discovered at Philmont Scout Ranch, New Mexico, in 1983 by American geologist Charles Pillmore. Originally thought to belong to a hadrosaurid, examination of the footprint revealed a large 'heel' unknown in ornithopod dinosaur tracks, and traces of what may have been a hallux, the dewclaw-like fourth digit of the tyrannosaur foot. The footprint was published as the ichnogenus Tyrannosauripus pillmorei in 1994, by Martin Lockley and Adrian Hunt. Lockley and Hunt suggested that it was very likely the track was made by a Tyrannosaurus rex, which would make it the first known footprint from this species. The track was made in what was once a vegetated wetland mud flat. It measures 83 centimeters (33 in) long by 71 centimeters (28 in) wide.^[126]

A second footprint that may have been made by a Tyrannosaurus was first reported in 2007 by British paleontologist Phil Manning, from the Hell Creek Formation of Montana. This second track measures 72 centimeters (28 in) long, shorter than the track described by Lockley and Hunt. Whether or not the track was made by Tyrannosaurus is unclear, though Tyrannosaurus and Nanotyrannus are the only large theropods known to have existed in the Hell Creek Formation.^[127][128]

A set of footprints in Glenrock, Wyoming dating to the Maastrichtian stage of the late cretaceous and hailing from the Lance Formation were described by Scott Persons, Phil Currie et al. in January 2016, and are believed to belong to either a juvenile Tyrannosaurus rex or the dubious tyrannosaurid Nanotyrannus lancensis. From measurements and based on the positions of the footprints, the animal was believed to be traveling at a walking speed of around 2.8 to 5 miles per hour and was estimated to have a hip height of 1.56 m (5.1 ft) to 2.06 m (6.8 ft).^{[129][130][131]} A follow-up paper appeared in 2017, increasing the speed estimations by 50-80 %.^[132]

Locomotion

Only known tyrannosaurid trackway (Bellatoripes fredlundi), from the Wapiti Formation, British Columbia

Scientists have produced a wide range of maximum running speed estimates for Tyrannosaurus, mostly around 11 meters per second (40 km/h; 25 mph), but a few as low as 5–11 meters per second (18–40 km/h; 11–25 mph), and a few as high as 20 meters per second (72 km/h; 45 mph). Researchers have to rely on various estimating techniques because, while there are many tracks of very large theropods walking, so far none have been found of very large theropods running—and this absence may indicate that they did not run.^[133] A 2002 paper in Nature used a mathematical model (validated by applying it to three living animals, alligators, chickens, and humans; later eight more species including emus and ostriches^[133]) to gauge the leg muscle mass needed for fast running (over 40 km/h or 25 mph).^[134] They found that proposed top speeds in excess of 40 kilometers per hour (25 mph) for Tyrannosaurus were infeasible, because they would require very large leg muscles (more than approximately 40–86% of total body mass). Even moderately fast speeds would have required large leg muscles. This discussion is difficult to resolve, as it is unknown how large the leg muscles actually were in Tyrannosaurus. If they were smaller, only 18 kilometers per hour (11 mph) walking or jogging might have been possible.^[134] A study in 2007 used computer models to estimate running speeds, based on data taken directly from fossils, and claimed that Tyrannosaurus rex had a top running speed of 8 meters per second (29 km/h; 18 mph). An average professional football (soccer) player would be slightly slower, while a human sprinter can reach 12 meters per second (43 km/h; 27 mph). These computer models predict a top speed of 17.8 meters per second (64 km/h; 40 mph) for a 3-kilogram (6.6 lb) Compsognathus^[135][136] (probably a juvenile individual).^[137]

Femur (thigh bone)

Tibia (shin bone)

Metatarsals (foot bones)

Dewclaw

Phalanges (toe bones)

Skeletal anatomy of a T. rex right leg

Jack Horner and Don Lessem argued in 1993 that Tyrannosaurus was slow and probably could not run (no airborne phase in mid-stride), because its ratio of femur (thigh bone) to tibia (shin bone) length was greater than 1, as in most large theropods and like a modern elephant.^[51] Christiansen (1998) estimated that the leg bones of Tyrannosaurus were not significantly stronger than those of elephants, which are relatively limited in their top speed and never actually run (there is no airborne phase), and hence proposed that the dinosaur's maximum speed would have been about 11 meters per second (40 km/h; 25 mph), which is about the speed of a human sprinter. But he also noted that such estimates depend on many dubious assumptions.^[138] A 2017 study found that an adult Tyrannosaurus was incapable of running due to very high skeletal loads. Using the latest computing technology and a calculated weight estimate of 7 tons. Their model showed that speeds above 11 mph (18 km/h) would have probably shattered the leg bones of Tyrannosaurus. The finding may mean that running was also not possible for other giant theropod dinosaurs like Giganotosaurus, Mapusaurus and Acrocanthosaurus.^[139]

A study in 2017 by researchers from the German Centre for Integrative Biodiversity Research (iDiv) found that the top speed of Tyrannosaurus was around 17 mph (27 km/h). Other dinosaurs including Triceratops, Velociraptor and Brachiosaurus were also analyzed in the study, as were many living animals like elephants, cheetahs and rabbits. It found that large animals like Tyrannosaurus exhaust their energy reserves long before they reach their theoretical top speed, resulting in a parabola-like relationship between size and speed. The equation can calculate the top speed of an animal with almost 90% accuracy and can be applied to both living and extinct animals.^[140][141] Farlow and colleagues (1995) have argued that a Tyrannosaurus weighing 5.4 metric tons (6.0 short tons) to 7.3 metric tons (8.0 short tons) would have been critically or even fatally injured if it had fallen while moving quickly, since its torso would have slammed into the ground at a deceleration of 6 g (six times the acceleration due to gravity, or about 60 meters/s²) and its tiny arms could not have reduced the impact.^[16] Giraffes have been known to gallop at 50 kilometers per hour (31 mph), despite the risk that they might break a leg or worse, which can be fatal even in a safe environment such as a zoo.^[142][143] Thus it is possible that Tyrannosaurus also moved fast when necessary and had to accept such risks.^[144][145]

Scientists who think that Tyrannosaurus was able to run point out that hollow bones and other features that would have lightened its body may have kept adult weight to a mere 4.5 metric tons (5.0 short tons) or so, or that other animals like ostriches and horses with long, flexible legs are able to achieve high speeds through slower but longer strides. Some have also argued that Tyrannosaurus had relatively larger leg muscles than any animal alive today, which could have enabled fast running at 40–70 kilometers per hour (25–43 mph).^[134] Holtz (1998) noted that tyrannosaurids and some closely related groups had significantly longer distal hindlimb components (shin plus foot plus toes) relative to the femur length than most other theropods, and that tyrannosaurids and their close relatives had a tightly interlocked metatarsus (foot bones) that more effectively transmitted locomotory forces from the foot to the lower leg than in earlier theropods He therefore concluded that tyrannosaurids and their close relatives were the fastest large theropods.^[146]

T. rex foot showing the compressed arctometatarsalian condition of the middle metatarsal, compared to that of Allosaurus

In one study, Gregory S. Paul pointed out that the flexed kneed and digitigrade adult Tyrannosaurus were much better adapted for running than elephants or humans, pointing out that Tyrannosaurus had a large ilium bone and cnemial crest that would have supported large muscles needed for running. He also mentioned that Alexander's (1989) formula to calculate speed by bone strength was only partly reliable. He suggests that the formula is overly sensitive to bone length; making long bones artificially weak. He also pointed out that the lowered risk of being wounded in combat may have been worth the risk of Tyrannosaurus falling while running.^[147] A 2003 also found that the tyrannosaurid arctometatarsals and elastic ligaments worked together in what he called a 'tensile keystone model' to strengthen the feet of Tyrannosaurus, increase the animal's stability and add greater resistance to dissociation over that of other theropod families; while still allowing resiliency that is otherwise reduced in modern animals with metapodia to a single element. The study suggested that the mechanism of storing and returning energy in the tendon could have worked efficiently in tyrannosaurids as they do in modern large vertebrates. The scientists also noted that the arctometatarsals may have enabled tyrannosaurid feet to absorb forces such as linear deceleration, lateral acceleration and torsion more effectively than those of other theropods. This could suggest that tyrannosaurids such as Tyrannosaurus had greater agility than other large theropods without an arctometatarsus.^[148]

Muscle mass reconstruction of M. caudofemoralis longus

A 2010 study proposed that Tyrannosaurus's speed may have been enhanced by strong tail muscles.^[149] The researchers found that theropods such as T. rex had certain muscle arrangements that are different from modern day birds and mammals but with some similarities to modern reptiles. They concluded that the caudofemoralis muscles which link the tail bones and the upper leg bones could have assisted Tyrannosaurus in leg retraction and enhanced its running ability, agility and balance. The caudofemoralis muscle would have been a key muscle in femoral retraction; pulling back the leg at the femur.^[149] The study also found that theropod skeletons such as those of Tyrannosaurus had adaptations (such as elevated transverse processes in the tail vertebrae) to enable the growth of larger tail muscles and that Tyrannosaurus's tail muscle mass may have been underestimated by over 25 percent and perhaps as much as 45 percent. ^[149] Mallison (2011), suggested that Tyrannosaurus and many other dinosaurs may have achieved relatively high speeds through short rapid strides instead of the long strides employed by modern birds and mammals when running, likening their movement to power-walking. This, according to Mallison, would have been achievable irrespective of joint strength and lessened the need for additional muscle mass in the legs, particularly at the ankles. John Hutchinson advised caution regarding this theory, suggesting that they must first look into dinosaur muscles to see how frequently they could have contracted.^[150]

Tyrannosaurus may have been faster than its prey species, hadrosaurids and ceratopsians.^[134] In addition, some advocates of the idea that Tyrannosaurus was a predator claim that tyrannosaur running speed is not important, since it may have been slow but still faster than its probable prey.^[151] Thomas Holtz also noted that Tyrannosaurus had proportionately longer feet than the animals it hunted: duck-billed dinosaurs and horned dinosaurs.^[93] Paul and Christiansen (2000) argued that at least the later ceratopsians had upright forelimbs and the larger species may have been as fast as rhinos.^[152] Tyrannosaurus may have been slow to turn, possibly taking one to two seconds to turn only 45° — an amount that humans, being vertically oriented and tailless, can spin in a fraction of a second.^[153] The cause of the difficulty is rotational inertia, since much of Tyrannosaurus' mass was some distance from its center of gravity, like a human carrying a heavy timber horizontally — although it might have reduced the average distance by arching its back and tail and pulling its head and forelimbs close to its body, rather like the way ice skaters pull their arms closer in order to spin faster.^[154]

Brain and senses

The eye-sockets faced mainly forwards, giving it good binocular vision (Sue specimen).

A study conducted by Lawrence Witmer and Ryan Ridgely of Ohio University found that Tyrannosaurus shared the heightened sensory abilities of other coelurosaurs, highlighting relatively rapid and coordinated eye and head movements, as well as an enhanced ability to sense low frequency sounds that would allow tyrannosaurs to track prey movements from long distances and an enhanced sense of smell.^[155] A study published by Kent Stevens of the University of Oregon concluded that Tyrannosaurus had keen vision. By applying modified perimetry to facial reconstructions of several dinosaurs including Tyrannosaurus, the study found that Tyrannosaurus had a binocular range of 55 degrees, surpassing that of modern hawks. Stevens also estimated that Tyrannosaurus had 13 times the visual acuity of a human, thereby surpassing the visual acuity of an eagle which is 3.6 times that of a person, and a limiting far point (that is the distance at which an object can be seen as separate from the horizon) as far as 6 km (3.7 mi) away, which is greater than the 1.6 km (1 mi) that a human can see.^{[24][25][156]}

Thomas Holtz Jr. would note that high depth perception of Tyrannosaurus may have been due to the prey it had to hunt, noting that it had to hunt horned dinosaurs such as Triceratops, armored dinosaurs such as Ankylosaurus, and the duck-billed dinosaurs and their possibly complex social behaviors. He would suggest that this made precision more crucial for Tyrannosaurus enabling it to, "get in, get that blow in and take it down." In contrast, Acrocanthosaurus had limited depth perception because they hunted large sauropods, which were relatively rare during the time of Tyrannosaurus.^[93]

Cast of the braincase at the Australian Museum, Sydney.

Tyrannosaurus had very large olfactory bulbs and olfactory nerves relative to their brain size, the organs responsible for a heightened sense of smell. This suggests that the sense of smell was highly developed, and implies that tyrannosaurs could detect carcasses by scent alone across great distances. The sense of smell in tyrannosaurs may have been comparable to modern vultures, which use scent to track carcasses for scavenging. Research on the olfactory bulbs has shown that Tyrannosaurus rex had the most highly developed sense of smell of 21 sampled non-avian dinosaur species.^[157]

Somewhat unusually among theropods, T. rex had a very long cochlea. The length of the cochlea is often related to hearing acuity, or at least the importance of hearing in behavior, implying that hearing was a particularly important sense to tyrannosaurs. Specifically, data suggests that Tyrannosaurus rex heard best in the low-frequency range, and that low-frequency sounds were an important part of tyrannosaur behavior.^[155]

A study by Grant R. Hurlburt, Ryan C. Ridgely and Lawrence Witmer obtained estimates for Encephalization Quotients (EQs), based on reptiles and birds, as well as estimates for the ratio of cerebrum to brain mass. The study concluded that Tyrannosaurus had the relatively largest brain of all adult non-avian dinosaurs with the exception of certain small maniraptoriforms (Bambiraptor, Troodon and Ornithomimus). The study found that Tyrannosaurus's relative brain size was still within the range of modern reptiles, being at most 2 standard deviations above the mean of non-avian reptile EQs. The estimates for the ratio of cerebrum mass to brain mass would range from 47.5 to 49.53 percent. According to the study, this is more than the lowest estimates for extant birds (44.6 percent), but still close to the typical ratios of the smallest sexually mature alligators which range from 45.9–47.9 percent.^[158]

Feeding strategies

Tyrannosaurus tooth marks on bones of various herbivorous dinosaurs

A study in 2012 by Karl Bates and Peter Falkingham demonstrated that Tyrannosaurus had the most powerful bite of any terrestrial animal that has ever lived. They found that an adult Tyrannosaurus could have exerted 35,000 to 57,000 N (7,868 to 12,814 lbf) of force in the back teeth.^{[159][160][161]} Even higher estimates were made by professor Mason B. Meers of the University of Tampa in 2003. In his study, Meers estimated a possible bite force of 183,000 to 235,000 N (41,140 to 52,830 lbf).^[9] A study in 2017 by Greg Erikson and Paul Gignac and published in the journal Scientific Reports found that Tyrannosaurus could exert bite forces of 8,526 N to 34,522 N (1,917 to 7,761 lbf) and tooth pressures of 718 to 2,974 MPa (104,137 to 431,342 psi). This allowed it to crush bones during repetitive biting and fully exploit the carcasses of large dinosaurs, giving it access to the mineral salts and marrow within bone that smaller carnivores could not access.^[162] Research done by Stephan Lautenschlager et al. from the University of Bristol, reveals Tyrannosaurus was also capable of a maximum jaw gape of around 80 degrees, a necessary adaptation for a wide range of jaw angles in order to power the creature's strong bite.^[163][164]

The debate about whether Tyrannosaurus was a predator or a pure scavenger is as old as the debate about its locomotion. Lambe (1917) described a good skeleton of Tyrannosaurus close relative Gorgosaurus and concluded that it and therefore also Tyrannosaurus was a pure scavenger, because the Gorgosaurus teeth showed hardly any wear.^[165] This argument is no longer taken seriously, because theropods replaced their teeth quite rapidly. Ever since the first discovery of Tyrannosaurus most scientists have speculated that it was a predator; like modern large predators it would readily scavenge or steal another predator's kill if it had the opportunity.^[166]

Paleontologist Jack Horner has been a major advocate of the idea that Tyrannosaurus was exclusively a scavenger and did not engage in active hunting at all,^{[51][167][168]} though Horner himself has claimed that he never published this idea in the peer-reviewed scientific literature and used it mainly as a tool to teach a popular audience, particularly children, the dangers of making assumptions in science (such as assuming T. rex was a hunter) without using evidence.^[169] Nevertheless, Horner presented several arguments in the popular literature to support the pure scavenger hypothesis:

• Tyrannosaur arms are short when compared to other known predators. Horner argues that the arms were too short to make the necessary gripping force to hold on to prey.^[170]
• Tyrannosaurs had large olfactory bulbs and olfactory nerves (relative to their brain size). These suggest a highly developed sense of smell which could sniff out carcasses over great distances, as modern vultures do. Research on the olfactory bulbs of dinosaurs has shown that Tyrannosaurus had the most highly developed sense of smell of 21 sampled dinosaurs.^[171] Opponents of the pure scavenger hypothesis have used the example of vultures in the opposite way, arguing that the scavenger hypothesis is implausible because the only modern pure scavengers are large gliding birds, which use their keen senses and energy-efficient gliding to cover vast areas economically.^[172] Researchers from Glasgow concluded that an ecosystem as productive as the current Serengeti would provide sufficient carrion for a large theropod scavenger, although the theropod might have had to be cold-blooded in order to get more calories from carrion than it spent on foraging (see Metabolism of dinosaurs). They also suggested that modern ecosystems like the Serengeti have no large terrestrial scavengers because gliding birds now do the job much more efficiently, while large theropods did not face competition for the scavenger ecological niche from gliding birds.^[173]
• Tyrannosaur teeth could crush bone, and therefore could extract as much food (bone marrow) as possible from carcass remnants, usually the least nutritious parts. Karen Chin and colleagues have found bone fragments in coprolites (fossilized feces) that they attribute to tyrannosaurs, but point out that a tyrannosaur's teeth were not well adapted to systematically chewing bone like hyenas do to extract marrow.^[174]
• Since at least some of Tyrannosaurus's potential prey could move quickly, evidence that it walked instead of ran could indicate that it was a scavenger.^[167][175] On the other hand, recent analyses suggest that Tyrannosaurus, while slower than large modern terrestrial predators, may well have been fast enough to prey on large hadrosaurs and ceratopsians.^[134][151]

Other evidence suggests hunting behavior in Tyrannosaurus. The eye sockets of tyrannosaurs are positioned so that the eyes would point forward, giving them binocular vision slightly better than that of modern hawks. Horner also pointed out that the tyrannosaur lineage had a history of steadily improving binocular vision. It is not obvious why natural selection would have favored this long-term trend if tyrannosaurs had been pure scavengers, which would not have needed the advanced depth perception that stereoscopic vision provides.^[24][25] In modern animals, binocular vision is found mainly in predators.

The damage to the tail vertebrae of this Edmontosaurus annectens skeleton (on display at the Denver Museum of Nature and Science) indicates that it may have been bitten by a Tyrannosaurus

A skeleton of the hadrosaurid Edmontosaurus annectens has been described from Montana with healed tyrannosaur-inflicted damage on its tail vertebrae. The fact that the damage seems to have healed suggests that the Edmontosaurus survived a tyrannosaur's attack on a living target, i.e. the tyrannosaur had attempted active predation.^[176] There is also evidence for an aggressive interaction between a Triceratops and a Tyrannosaurus in the form of partially healed tyrannosaur tooth marks on a Triceratops brow horn and squamosal (a bone of the neck frill); the bitten horn is also broken, with new bone growth after the break. It is not known what the exact nature of the interaction was, though: either animal could have been the aggressor.^[177] Since the Triceratops wounds healed, it is most likely that the Triceratops survived the encounter and managed to overcome the Tyrannosaurus. Paleontologist Peter Dodson estimates that in a battle against a bull Triceratops, the Triceratops had the upper hand and would successfully defend itself by inflicting fatal wounds to the Tyrannosaurus using its sharp horns.^[178]

When examining Sue, paleontologist Pete Larson found a broken and healed fibula and tail vertebrae, scarred facial bones and a tooth from another Tyrannosaurus embedded in a neck vertebra. If correct, these might be strong evidence for aggressive behavior between tyrannosaurs but whether it would have been competition for food and mates or active cannibalism is unclear.^[179] Further recent investigation of these purported wounds has shown that most are infections rather than injuries (or simply damage to the fossil after death) and the few injuries are too general to be indicative of intraspecific conflict.^[167] Some researchers argue that if Tyrannosaurus were a scavenger, another dinosaur had to be the top predator in the Amerasian Upper Cretaceous. Top prey were the larger marginocephalians and ornithopods. The other tyrannosaurids share so many characteristics that only small dromaeosaurs and troodontids remain as feasible top predators. In this light, scavenger hypothesis adherents have suggested that the size and power of tyrannosaurs allowed them to steal kills from smaller predators,^[175] although they may have had a hard time finding enough meat to scavenge, being outnumbered by smaller theropods.^[180] Most paleontologists accept that Tyrannosaurus was both an active predator and a scavenger like most large carnivores.^[11]

Two teeth from the lower jaw of specimen MOR 1125, "B-rex", showing the variation in tooth size within an individual

Tyrannosaurus may have had infectious saliva used to kill its prey. This theory was first proposed by William Abler.^[181] Abler examined the teeth of tyrannosaurids between each tooth serration; the serrations may have held pieces of carcass with bacteria, giving Tyrannosaurus a deadly, infectious bite much like the Komodo dragon was thought to have. Jack Horner regards Tyrannosaurus tooth serrations as more like cubes in shape than the serrations on a Komodo monitor's teeth, which are rounded.^[182] All forms of saliva contain possibly hazardous bacteria, so the prospect of it being used as a method of predation is disputable.

Tyrannosaurus, and most other theropods, probably primarily processed carcasses with lateral shakes of the head, like crocodilians. The head was not as maneuverable as the skulls of allosauroids, due to flat joints of the neck vertebrae.^[183]

Pack behavior

Mounted skeletons of different age groups, Los Angeles Natural History Museum

Philip J. Currie of the University of Alberta has suggested that Tyrannosaurus may have been pack animals. Currie compared Tyrannosaurus rex favorably to related species Tarbosaurus bataar and Albertosaurus sarcophagus, fossil evidence from which Currie had previously used to suggest that they lived in packs.^[186] Currie pointed out that a find in South Dakota preserved three Tyrannosaurus rex skeletons in close proximity to each other.^[187] After using CT scanning, Currie stated that Tyrannosaurus would have been capable of such complex behavior, because its brain size is three times greater than what would be expected for an animal of its size. Currie elaborated that Tyrannosaurus had a larger brain-to-body-size proportion than crocodiles and three times more than plant eating dinosaurs such as Triceratops of the same size. Currie believed Tyrannosaurus to be six times smarter than most dinosaurs and other reptiles.^[186][188] Because the available prey, such as Triceratops and Ankylosaurus, were well-armored, and that others were fast-moving, it would have been necessary for Tyrannosaurus to hunt in groups. Currie speculated that juveniles and adults would have hunted together, with the faster juveniles chasing down the prey and the more powerful adults making the kill, by analogy to modern-day pack hunters where each member contributes a skill.^[186]

Currie's pack-hunting hypothesis has been harshly criticized by other scientists. Brian Switek, writing for The Guardian in 2011,^[189] noted that Currie's pack hypothesis has not been presented as research in a peer-reviewed scientific journal, but primarily in relation to a television special and tie-in book called Dino Gangs. Switek also noted that Currie's argument for pack hunting in Tyrannosaurus rex is primarily based on analogy to a different species, Tarbosaurus bataar, and that the supposed evidence for pack hunting in T. bataar itself has not yet been published and subjected to scientific scrutiny. According to Switek and other scientists who have participated in panel discussions about the Dino Gangs television program, the evidence for pack hunting in Tarbosaurus and Albertosaurus is weak, based primarily on the association of several skeletons, for which numerous alternative explanations have been proposed (e.g. drought or floods forcing numerous specimens together to die in one place). In fact, Switek notes that the Albertosaurus bonebed site, on which Currie has based most of the interpretations of supposed pack hunting in related species, preserves geological evidence of just such a flood. Switek said, "bones alone are not enough to reconstruct dinosaur behaviour. The geological context in which those bones are found – the intricate details of ancient environments and the pace of prehistoric time – are essential to investigating the lives and deaths of dinosaurs,"^[189] and noted that Currie must first describe the geological evidence from other tyrannosaur bonebed sites before jumping to conclusions about social behavior. Switek described the sensational claims provided in press releases and news stories surrounding the Dino Gangs program as "nauseating hype" and noted that the production company responsible for the program, Atlantic Productions, has a poor record involving exaggerating claims about new fossil discoveries, most notably the controversial claim it published regarding the supposed early human ancestor Darwinius, which soon turned out to be a relative of lemurs instead.^[189]

Nonetheless, in 2014, McCrea et al. presented evidences of gregarious behavior in the form of fossilized trackways found in northeastern British Columbia, Canada, that were left by three Tyrannosaurus heading towards the same direction.^[190][191]

Pathology

Restoration of an individual (based on MOR 980) with parasite infections

In 2001, Bruce Rothschild and others published a study examining evidence for stress fractures and tendon avulsions in theropod dinosaurs and the implications for their behavior. Since stress fractures are caused by repeated trauma rather than singular events they are more likely to be caused by regular behavior than other types of injuries. Of the 81 Tyrannosaurus foot bones examined in the study one was found to have a stress fracture, while none of the 10 hand bones were found to have stress fractures. The researchers found tendon avulsions only among Tyrannosaurus and Allosaurus. An avulsion injury left a divot on the humerus of Sue the T. rex, apparently located at the origin of the deltoid or teres major muscles. The presence of avulsion injuries being limited to the forelimb and shoulder in both Tyrannosaurus and Allosaurus suggests that theropods may have had a musculature more complex than and functionally different from those of birds. The researchers concluded that Sue's tendon avulsion was probably obtained from struggling prey. The presence of stress fractures and tendon avulsions in general provides evidence for a "very active" predation-based diet rather than obligate scavenging.^[192]

A 2009 study showed that holes in the skulls of several specimens that were previously explained by intraspecific attacks might have been caused by Trichomonas-like parasites that commonly infect avians.^[193] Further evidence of intraspecific attack were found by Joseph Peterson and his colleagues in the juvenile Tyrannosaurus nicknamed Jane. Peterson and his team found that Jane's skull showed healed puncture wounds on the upper jaw and snout which they believe came from another juvenile Tyrannosaurus. Subsequent CT scans of Jane's skull would further confirm the team's hypothesis, showing that the puncture wounds came from a traumatic injury and that there was subsequent healing.^[194] The team would also state that Jane's injuries were structurally different from the parasite-induced lesions found in Sue and that Jane's injuries were on her face whereas the parasite that infected Sue caused lesions to the lower jaw.^[195]