Gorgosaurus

''Gorgosaurus'' ( ; ) is a genus of tyrannosaurid theropod dinosaur that lived in western North America during the Late Cretaceous Period (Campanian), between about 76.5 and 75 million years ago. Fossil remains have been found in the Canadian province of Alberta and the U.S. state of Montana. Paleontologists recognize only the type species, ''G. libratus'', although other species have been erroneously referred to the genus.

Like most known tyrannosaurids, ''Gorgosaurus'' was a large bipedal predator, measuring in length and in body mass. Dozens of large, sharp teeth lined its jaws, while its two-fingered forelimbs were comparatively small. ''Gorgosaurus'' was most closely related to ''Albertosaurus'', and more distantly related to the larger ''Tyrannosaurus''. ''Gorgosaurus'' and ''Albertosaurus'' are extremely similar, distinguished mainly by subtle differences in the teeth and skull bones. Some experts consider ''G. libratus'' to be a species of ''Albertosaurus''; this would make ''Gorgosaurus'' a junior synonym of that genus.

''Gorgosaurus'' lived in a lush floodplain environment along the edge of an inland sea. It was an apex predator, preying upon abundant ceratopsids and hadrosaurs. In some areas, ''Gorgosaurus'' coexisted with another tyrannosaurid, '' Daspletosaurus''. Although these animals were roughly the same size, there is some evidence of niche differentiation between the two. ''Gorgosaurus'' is the best-represented tyrannosaurid in the fossil record, known from dozens of specimens. These plentiful remains have allowed scientists to investigate its ontogeny, life history and other aspects of its biology.

Discovery and naming

''Gorgosaurus libratus'' was first described by Lawrence Lambe in 1914. Its name is derived from the Greek (''gorgos'' – "fierce" or "terrible") and (''saurus'' – "lizard"). The type species is ''G. libratus''; the specific epithet "balanced" is the past participle of the Latin verb ''librare'', meaning "to balance".

The holotype of ''Gorgosaurus libratus'' ( NMC 2120) is a nearly complete skeleton associated with a skull, discovered in 1913 by Charles M. Sternberg. This specimen was the first tyrannosaurid found with a complete hand. It was found in the Dinosaur Park Formation of Alberta and is housed in the Canadian Museum of Nature in Ottawa. Prospectors from the American Museum of Natural History in New York City were active along the Red Deer River in Alberta at the same time, collecting hundreds of spectacular dinosaur specimens, including four complete ''G. libratus'' skulls, three of which were associated with skeletons. Matthew and Brown described four of these specimens in 1923.

Matthew and Brown also described a fifth skeleton ( AMNH 5664), which Charles H. Sternberg had collected in 1917 and sold to their museum. It was smaller than other ''Gorgosaurus'' specimens, with a lower, lighter skull and more elongate limb proportions. Many sutures between bones were unfused in this specimen as well. Matthew and Brown noted that these features were characteristic of juvenile tyrannosaurids, but still described it as the holotype of a new species, ''G. sternbergi''. Today's paleontologists regard this specimen as a juvenile ''G. libratus''. Dozens of other specimens have been excavated from the Dinosaur Park Formation and are housed in museums across the United States and Canada. ''G. libratus'' is the best-represented tyrannosaurid in the fossil record, known from a virtually complete growth series.

In 1856, Joseph Leidy described two tyrannosaurid premaxillary teeth from Montana. Although there was no indication of what the animal looked like, the teeth were large and robust, and Leidy gave them the name '' Deinodon''. Matthew and Brown commented in 1922 that these teeth were indistinguishable from those of ''Gorgosaurus'', but in the absence of skeletal remains of ''Deinodon'', opted not to unequivocally synonymize the two genera, provisionally naming a ''?Deinodon libratus''. Although ''Deinodon'' teeth are very similar to those of ''Gorgosaurus'', tyrannosaurid teeth are extremely uniform, so it cannot be said for certain which animal they belonged to. ''Deinodon'' is usually regarded as a ''nomen dubium'' today. Additional likely synonyms of ''G. libratus'' and/or ''D. horridus'' include '' Laelaps falculus'', '' Laelaps hazenianus'', ''Laelaps incrassatus'', and '' Dryptosaurus kenabekides''.

Several tyrannosaurid skeletons from the Two Medicine Formation and Judith River Formation of Montana probably belong to ''Gorgosaurus'', although it remains uncertain whether they belong to ''G. libratus'' or a new species. One specimen from Montana ( TCMI 2001.89.1), housed in the Children's Museum of Indianapolis, shows evidence of severe pathologies, including healed leg, rib, and vertebral fractures, osteomyelitis (infection) at the tip of the lower jaw resulting in permanent tooth loss, and possibly a brain tumor.

Formerly assigned species

Several species were incorrectly assigned to ''Gorgosaurus'' in the 20th century. A complete skull of a small tyrannosaurid ( CMNH 7541), found in the younger, late Maastrichtian-age Hell Creek Formation of Montana, was named ''Gorgosaurus lancensis'' by Charles Whitney Gilmore in 1946. This specimen was renamed '' Nanotyrannus'' by Bob Bakker and colleagues in 1988. Currently, many paleontologists regard ''Nanotyrannus'' as a juvenile ''Tyrannosaurus rex''. Similarly, Evgeny Maleev created the names ''Gorgosaurus lancinator'' and ''Gorgosaurus novojilovi'' for two small tyrannosaurid specimens ( PIN 553-1 and PIN 552–2) from the Nemegt Formation of Mongolia in 1955. Kenneth Carpenter renamed the smaller specimen '' Maleevosaurus novojilovi'' in 1992, but both are now considered juveniles of '' Tarbosaurus bataar''.

Description

''Gorgosaurus'' was smaller than ''Tyrannosaurus'' or ''Tarbosaurus'', close in size to ''Albertosaurus''. Adults reached in length from snout to tail, and weighed in body mass. The largest known skull measures long, just slightly smaller than that of ''Daspletosaurus''. As in other tyrannosaurids, the skull was large compared to its body size, although chambers within the skull bones and large openings (fenestrae) between bones reduced its weight. ''Albertosaurus'' and ''Gorgosaurus'' share proportionally longer and lower skulls than ''Daspletosaurus'' and other tyrannosaurids. The end of the snout was blunt, and the nasal and parietal bones were fused along the midline of the skull, as in all other members of the family. The eye socket was circular rather than oval or keyhole-shaped as in other tyrannosaurid genera. A tall crest rose from the lacrimal bone in front of each eye, similar to ''Albertosaurus'' and ''Daspletosaurus''. Differences in the shape of bones surrounding the brain set ''Gorgosaurus'' apart from ''Albertosaurus''.

''Gorgosaurus'' teeth were typical of all known tyrannosaurids. The eight premaxillary teeth at the front of the snout were smaller than the rest, closely packed and ''D''-shaped in cross section. In ''Gorgosaurus'', the first tooth in the maxilla was also shaped like the premaxillary teeth. The rest of the teeth were oval in cross section, rather than blade-like as in most other theropods. Along with the eight premaxillary teeth, ''Gorgosaurus'' had 26 to 30 maxillary teeth and 30 to 34 teeth in the dentary bones of the lower jaw. This number of teeth is similar to ''Albertosaurus'' and ''Daspletosaurus'' but is fewer than those of ''Tarbosaurus'' or ''Tyrannosaurus''.
''Gorgosaurus'' shared its general body plan with all other tyrannosaurids. Its massive head was perched on the end of an ''S''-shaped neck. In contrast to its large head, its forelimbs were very small. The forelimbs had only two digits, although a third metacarpal is known in some specimens, the vestigial remains of the third digit seen in other theropods. ''Gorgosaurus'' had four digits on each hindlimb, including a small first toe (hallux) which did not contact the ground. Tyrannosaurid hindlimbs were long relative to overall body size compared with other theropods. The largest known ''Gorgosaurus'' femur measured long. In several smaller specimens of ''Gorgosaurus'', the tibia was longer than the femur, a proportion typical of fast-running animals. The two bones were of equal length in the largest specimens. The long, heavy tail served as a counterweight to the head and torso and placed the center of gravity over the hips.

In 2001, paleontologist Phil Currie reported skin impressions from the holotype specimen of ''G. libratus''. He originally reported the skin as being essentially smooth and lacking the scales found in other dinosaurs, similar to the secondarily featherless skin found in large modern birds.Currie, P. (2001). 2001 A. Watson Armour Symposium: The Paleobiology and Phylogenetics of Large Theropods. Field Museum of Natural History, Chicago. Scales of some sort were present in this specimen, but they are reportedly widely dispersed from each other and very small. Other patches of isolated ''Gorgosaurus'' skin shows denser, and larger though still relatively fine scales (smaller than hadrosaurid scales and approximately as fine as a Gila monster's).Holtz, T. 2001. Phil Currie celebration, tyrant skin, and other things. Dinosaur Mailing List post. http://dml.cmnh.org/2001Jul/msg00243.html . Accessed: March 15, 2014 Neither of these specimens was associated with any particular bone or specific body area. In the ''Encyclopedia of Dinosaurs'' Kenneth Carpenter pointed out that traces of skin impressions from the tail of ''Gorgosaurus'' showed similar small rounded or hexagonal scales.

Classification and systematics

''Gorgosaurus'' is classified in the theropod subfamily Albertosaurinae within the family Tyrannosauridae. It is most closely related to the slightly younger ''Albertosaurus''. These are the only two definite albertosaurine genera that have been described, although other undescribed species may exist. '' Appalachiosaurus'' was described as a basal tyrannosauroid just outside Tyrannosauridae, although American paleontologist Thomas Holtz published a phylogenetic analysis in 2004 which indicated it was an albertosaurine. More recent, unpublished work by Holtz agrees with the original assessment. All other tyrannosaurid genera, including ''Daspletosaurus'', ''Tarbosaurus'' and ''Tyrannosaurus'', are classified in the subfamily Tyrannosaurinae. Compared to the tyrannosaurines, albertosaurines had slender builds, with proportionately smaller, lower skulls and longer bones of the lower leg (tibia) and feet (metatarsals and phalanges).

The close similarities between ''Gorgosaurus libratus'' and ''Albertosaurus sarcophagus'' have led many experts to combine them into one genus over the years. ''Albertosaurus'' was named first, so by convention it is given priority over the name ''Gorgosaurus'', which is sometimes considered its junior synonym. William Diller Matthew and Barnum Brown doubted the distinction of the two genera as early as 1922. ''Gorgosaurus libratus'' was formally reassigned to ''Albertosaurus'' (as ''Albertosaurus libratus'') by Dale Russell in 1970, and many subsequent authors followed his lead. Combining the two greatly expands the geographical and chronological range of the genus ''Albertosaurus''. Other experts maintain the two genera as separate. Canadian paleontologist Phil Currie claims there are as many anatomical differences between ''Albertosaurus'' and ''Gorgosaurus'' as there are between ''Daspletosaurus'' and ''Tyrannosaurus'', which are almost always kept separate. He also notes that undescribed tyrannosaurids discovered in Alaska, New Mexico and elsewhere in North America may help clarify the situation. Gregory S. Paul has suggested that ''Gorgosaurus libratus'' is ancestral to ''Albertosaurus sarcophagus''.Paul. G.S. ''The Princeton Field Guide to Dinosaurs'', Princeton University Press, 2010. P. 105.

Below is the cladogram of Tyrannosauridae based on the phylogenetic analysis conducted by Loewen ''et al.'' in 2013.

Paleobiology

Diet and feeding

Just like other tyrannosaurids, bite force of ''Gorgosaurus'' and ''Albertosaurus'' increases slowly among young individuals, and then it increases exponentially when they reach the late juvenile stage. In 2012, Jovannelly and Lane estimated that ''Gorgosaurus'' could exert a bite force of at least 22,000, possibly up to 42,000 newtons. Other paleontologists have produced significantly lower bite force estimates. In 2021, given that the largest known ''Gorgosaurus'' had a similar bite force to the similar-sized ''Tyrannosaurus'', Therrien and colleagues proposed that the maximum bite force that could be produced by adult albertosaurines is around 12,200 to 21,800 newtons. In 2022, Sakamoto estimated that ''Gorgosaurus'' had an anterior bite force of 6,418 newtons and a posterior bite force of 13,817 newtons.

In 2023, a juvenile ''Gorgosaurus'' (TMP 2009.12.14) with its ''in situ'' stomach contents containing two ''Citipes'' juveniles about a year old intact was reported from the Dinosaur Park Formation. This juvenile would have been 5-7 years old at the time of death, measuring about long and weighing around . It is much larger than the two ''Citipes'' juveniles that weigh about , contrary to the assumption that tyrannosaurids fed on prey of their size once they reached , indicating that juvenile tyrannosaurids still consumed much smaller prey after exceeding a certain size threshold. It’s a direct dietary evidence that reinforces the theory of 'ontogenetic dietary shift' for tyrannosaurids, as previously inferred by ecological modeling and anatomical features among different age groups. Only the remains of the hindlimbs and caudal vertebrae of juvenile ''Citipes'' were present in the tyrannosaurid's stomach cavity, suggesting that a juvenile ''Gorgosaurus'' may have had preferential consumption of the muscular hindlimbs. Thomas R. Holtz Jr., a paleontologist who also previously theorized that tyrannosaurs underwent a big dietary shift with maturation, said that the fossil "looks like it was Thanksgiving," as the juvenile ''Gorgosaurus'' was mostly eating the legs of ''Citipes''.

Life history

Gregory Erickson and colleagues have studied the growth and life history of tyrannosaurids using bone histology, which can determine the age of a specimen when it died. A growth curve can be developed when the ages of various individuals are plotted against their sizes on a graph. Tyrannosaurids grew throughout their lives, but underwent tremendous growth spurts for about four years, after an extended juvenile phase. Sexual maturity may have ended this rapid growth phase, after which growth slowed down considerably in adult animals. Examining five ''Gorgosaurus'' specimens of various sizes, Erickson calculated a maximum growth rate of about per year during the rapid growth phase, slower than in tyrannosaurines like ''Daspletosaurus'' and ''Tyrannosaurus'', but comparable to ''Albertosaurus''.

''Gorgosaurus'' spent as much as half its life in the juvenile phase before ballooning up to near-maximum size in only a few years. This, along with the complete lack of predators intermediate in size between huge adult tyrannosaurids and other small theropods, suggests that these niches may have been filled by juvenile tyrannosaurids. This pattern is seen in modern Komodo dragons, whose hatchlings start off as tree-dwelling insectivores and slowly mature into massive apex predators capable of taking down large vertebrates. Other tyrannosaurids, including ''Albertosaurus'', have been found in aggregations that some have suggested to represent mixed-age packs, but there is no evidence of gregarious behavior in ''Gorgosaurus''. ot printed until 2000/ref>

The discovery of two exceptionally preserved juvenile skulls from ''Gorgosaurus'' suggests that ''Gorgosaurus'' underwent the morphological shift from gracile juveniles to robust adults at an earlier age than ''Tyrannosaurus'', to which it was compared in a study published by Jared Voris ''et al.,'' suggests that the ontogenetic changes occurred at roughly 5-7 years of age in ''Gorgosaurus''; much earlier than its larger and later relative. However, both tyrannosaur genera underwent these ontogenetic transformations at a similar percent of skull length relative to the large known adult individuals. The study's results likewise indicate that there is a dissociation between body size and cranial development in tyrannosaurs, while simultaneously allowing better identification of juvenile remains that may have been misidentified in museum fossil collections. It is estimated that an ontogenetic dietary shift of ''Gorgosaurus'' and ''Albertosaurus'' occurs when the mandibular length reaches , indicating that this is the stage when their bite force increases exponentially and when they begin to pursuit large prey.

Paleopathology

Several pathologies have been documented in the ''Gorgosaurus libratus'' holotype, NMC 2120. These include the third right dorsal rib, as well as healed fractures on the 13th and 14th gastralia and left fibula. Its fourth left metatarsal bore roughened exostoses both in the middle and at the far end. The third phalanx of the third right toe is deformed, as the claw on that digit has been described as "quite small and amorphous". The three pathologies may have been received in a single encounter with another dinosaur.Rothschild, B., Tanke, D. H., and Ford, T. L., 2001, Theropod stress fractures and tendon avulsions as a clue to activity: In: Mesozoic Vertebrate Life, edited by Tanke, D. H., and Carpenter, K., Indiana University Press, p. 331–336.

Another specimen cataloged as TMP94.12.602 bears multiple pathologies. A longitudinal fracture is present in the middle of the right fibula's shaft. Multiple ribs bear healed fractures and the specimen had a pseudoarthortic gastralium. Lesions from a bite received to the face were present and showed evidence that the wounds were healing before the animal died.

Another specimen has a poorly healed fracture of the right fibula, which left a large callus on the bone. In a 2001 study conducted by Bruce Rothschild and other paleontologists, 54 foot bones referred to ''Gorgosaurus'' were examined for signs of stress fracture, but none were found.Molnar, R. E., 2001, Theropod paleopathology: a literature survey: In: Mesozoic Vertebrate Life, edited by Tanke, D. H., and Carpenter, K., Indiana University Press, p. 337–363.

As with many tyrannosaurids, several ''Gorgosaurus'' specimens show evidence of intraspecific face biting.

Specimen TMP 1994.143.1, a juvenile skull from the Dinosaur Park Formation with several tyrannosaur bite marks, was previously believed to be '' Daspletosaurus'' sp. but was later assigned to ''Gorgosaurus libratus''.

TMP 2017.012.0002, is a ''Gorgosaurus'' right maxilla with 5 raised scars; healed injuries from face biting by conspecifics.

TMP91.36.500 is a very complete sub-adult ''Gorgosaurus'' with preserved face bite injuries and also has a thoroughly healed fracture in the right fibula. Also present was a healed fracture in the dentary and what the authors describing the specimen referred to as "a mushroom-like hyperostosis of a right pedal phalanx." Ralph Molnar has speculated that this may be the same kind of pathology afflicting an unidentified ornithomimid discovered with a similar mushroom shaped growth on a toe bone. TMP91.36.500 is also preserved in a characteristic death pose.

Paleoenvironment

Most specimens of ''Gorgosaurus libratus'' have been recovered from the Dinosaur Park Formation in Alberta. This formation dates to the middle of the Campanian, between 76.5 and 74.8 million years ago,Eberth, D.A. (2005). "The geology." In: Currie, P.J., and Koppelhus, E.B. (eds), ''Dinosaur Provincial Park: A Spectacular Ancient Ecosystem Revealed''. Indiana University Press: Bloomington and Indianapolis, 54–82. and ''Gorgosaurus libratus'' fossils are known specifically from the lower to middle section of the formation, between 76.6 and 75.1 million years ago. The Two Medicine Formation and Judith River Formation of Montana have also yielded possible ''Gorgosaurus'' remains. At this time, the area was a coastal plain along the western edge of the Western Interior Seaway, which divided North America in half. The Laramide Orogeny had begun uplifting the Rocky Mountains to the west, from which flowed great rivers that deposited eroded sediment in vast floodplains along the coast. The climate was subtropical with marked seasonality, and periodic droughts sometimes resulted in massive mortality among the great herds of dinosaurs, as represented in the numerous bonebed deposits preserved in the Dinosaur Park Formation. Conifers formed the forest canopy, while the understory plants consisted of ferns, tree ferns and angiosperms. Around 73 million years ago, the seaway began to expand, transgressing into areas formerly above sea level and drowning the Dinosaur Park ecosystem. This transgression, called the Bearpaw Sea, is recorded by the marine sediments of the massive Bearpaw Shale.

The Dinosaur Park Formation preserves a great wealth of vertebrate fossils. A wide variety of fish swam the rivers and estuaries, including gars, sturgeons, sharks and rays, among others. Frogs, salamanders, turtles, crocodilians and champsosaurs also dwelled in the aquatic habitats. Azhdarchid pterosaurs and ornithuran birds like '' Apatornis'' flew overhead, while the enantiornithine bird '' Avisaurus'' lived on the ground alongside multituberculate, metatherian and eutherian mammals. A number of species of terrestrial lizards were also present, including whiptails, skinks, monitors and alligator lizards. Dinosaur fossils in particular are found with unrivaled abundance and diversity. Huge herds of ceratopsids roamed the floodplains alongside equally large groups of saurolophine and lambeosaurine hadrosaurs. Other herbivorous groups like ornithomimids, therizinosaurs, pachycephalosaurs, small ornithopods, nodosaurids and ankylosaurids were also represented. Small predatory dinosaurs like oviraptorosaurs, troodonts and dromaeosaurs hunted smaller prey than the huge tyrannosaurids; ''Daspletosaurus'' and ''Gorgosaurus'', which were two orders of magnitude larger in mass. Intervening predatory niches may have been filled by young tyrannosaurids. A ''Saurornitholestes'' dentary has been discovered in the Dinosaur Park Formation that bore tooth marks left by the bite of a young tyrannosaur, possibly ''Gorgosaurus''.Jacobsen, A.R. 2001. Tooth-marked small theropod bone: An extremely rare trace. p. 58–63. In: ''Mesozoic Vertebrate Life''. Ed.s Tanke, D. H., Carpenter, K., Skrepnick, M. W. Indiana University Press.

Coexistence with ''Daspletosaurus''

In the middle stages of the Dinosaur Park Formation, ''Gorgosaurus'' lived alongside a rarer species of tyrannosaurid, ''Daspletosaurus''. This is one of the few examples of two tyrannosaur genera coexisting. Similar-sized predators in modern predator guilds are separated into different ecological niches by anatomical, behavioral or geographical differences that limit competition. Niche differentiation between the Dinosaur Park tyrannosaurids is not well understood. In 1970, Dale Russell hypothesized that the more common ''Gorgosaurus'' actively hunted fleet-footed hadrosaurs, while the rarer and more troublesome ceratopsians and ankylosaurians (horned and heavily armoured dinosaurs) were left to the more heavy built '' Daspletosaurus''. However, a specimen of ''Daspletosaurus'' ( OTM 200) from the contemporaneous Two Medicine Formation of Montana preserves the digested remains of a juvenile hadrosaur in its gut region, and another bonebed contains the remains of three ''Daspletosaurus'' along with the remains of at least five hadrosaurs.

Unlike some other groups of dinosaurs, neither genus was more common at higher or lower elevations than the other. However, ''Gorgosaurus'' appears more common in northern formations like Dinosaur Park, with species of ''Daspletosaurus'' being more abundant to the south. The same pattern is seen in other groups of dinosaurs. Chasmosaurine ceratopsians and saurolophine hadrosaurs are also more common in the Two Medicine Formation of Montana and in southwestern North America during the Campanian, while centrosaurines and lambeosaurines dominate in northern latitudes. Holtz has suggested this pattern indicates shared ecological preferences between tyrannosaurines, chasmosaurines and saurolophines. At the end of the later Maastrichtian stage, tyrannosaurines like ''Tyrannosaurus rex'', saurolophines like ''Edmontosaurus'' and '' Kritosaurus'' and chasmosaurines like ''Triceratops'' and ''Torosaurus'' were widespread throughout western North America, while lambeosaurines were rare, consisting of a few species like ''Hypacrosaurus'', and albertosaurines and centrosaurines had gone extinct. However, in the case of the centrosaurines, they had thrived in Asia with genera like '' Sinoceratops''. While albertosaurine remains have been found in the Hell Creek Formation, it is most likely these are indeterminate remains belonging to a species of ''Tyrannosaurus''.

See also

* Timeline of tyrannosaur research

References

External links

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Tyrannosauridae
Dinosaur genera
Campanian dinosaurs
Dinosaur Park Formation
Two Medicine Formation
Judith River Formation
Fossil taxa described in 1914
Taxa named by Lawrence Lambe
Dinosaurs of Canada
Dinosaurs of the United States