| Tyrannotitan | |
|---|---|
 | |
| Reconstructed skeleton inQueensland Museum | |
Scientific classification | |
| Kingdom: | Animalia |
| Phylum: | Chordata |
| Class: | Reptilia |
| Clade: | Dinosauria |
| Clade: | Saurischia |
| Clade: | Theropoda |
| Family: | †Carcharodontosauridae |
| Tribe: | †Giganotosaurini |
| Genus: | †Tyrannotitan Novas et al.,2005 |
| Type species | |
| †Tyrannotitan chubutensis Novas et al., 2005 | |
Tyrannotitan (/tɪˌrænəˈtaɪtən/;lit. 'tyrant titan') is a genus of largetheropoddinosaur belonging to thecarcharodontosaurid family. It is known from a single species,T. chubutensis, which lived during theAlbian stage of theEarly Cretaceous period in what is nowArgentina.Tyrannotitan is considered to share a close relationship with other prominent South American carcharodontosaurids such asGiganotosaurus andMapusaurus. Unlike its relatives, it was bulkier and more robust. This taxon is known from two specimens, both of which are highly incomplete.
Tyrannotitan chubutensis was described by Fernando E. Novas, Silvina de Valais, Pat Vickers-Rich, and Tom Rich in 2005. The fossils were found at La Juanita Farm, 28 kilometres (17 mi) northeast of Paso de Indios,Chubut Province, Argentina. They are believed to have been from the Cerro Castaño Member,Cerro Barcino Formation (Albianstage).[1]
Theholotype material was designated MPEF-PV 1156 and included partialdentaries, teeth, backvertebrae 3–8 and 11–14,proximal tail vertebrae, ribs andchevrons, a fragmentaryscapulocoracoid,humerus,ulna, partialilium, a nearly completefemur,fibula, and leftmetatarsal 2. Additional material (designated MPEF-PV 1157) includedjugals, a right dentary, teeth,atlas vertebra, neck vertebra (?) 9, back vertebrae (?)7, 10, 13, fusedsacral centra (5 total), an assortment ofdistal caudals, ribs, the right femur, a fragmentary left metatarsal 2, pedalphalanges 2-1, 2–2, and 3-3.[1]
Tyrannotitan was a large reptile, reaching 11.6 metres (38 ft) in length and 6–7.4 t (6.6–8.2 short tons) in body mass.[2][3][4][5][6] Its vertebral column is extensively pneumatized, with pneumatic openings in the dorsal and caudal vertebrae resembling those ofGiganotosaurus andMapusaurus.[7] More unusually,Tyrannotitan shows a pneumatic hiatus in the anterior sacral region, a gap in the invasive pneumaticity of different portions of the vertebral column that were pneumatized by independent segments of the respiratory system (air sacs or their diverticula).[7] Such gaps are most commonly observed in juvenile individuals, whose skeletal pneumaticity has not yet fully developed.[8]
Thescapulocoracoid is fused, and much better developed than that ofGiganotosauruscarolinii, yet the arm is very small. Most of the shaft of thescapula is missing.[1] Theacromion curves about 90 degrees from the shaft axis, making it look vaguelytyrannosaurid-like. Whether the sharp difference between taxa is due to evolution orsexual dimorphism in poorly sampled populations of both species, has not been determined (the latter seems unlikely). A proximal caudal has a very tall neural spine (about twice the height of its centrum, judging by the figure). The base of the orbitalfenestra is a notch of nearly 90 degrees into the body of thejugal, which contrasts with the rounded base restored forGiganotosaurus and agrees withCarcharodontosaurus favorably. The denticles on its teeth are "chisel-like", and are virtually identical to those of other carcharodontosaurids in having a wrinkled enamel surface, heavily serrated mesial and distal carinae, and labiolingually compressed (laterally flattened) crowns.[7] The femur of the paratype specimen is 1.4 m (4.6 ft) long according to Novas et al.[1] Canale et al. recoverTyrannotitan as deeply nested within the tribe Giganotosaurini as its most basal member. Characteristics that unite the Giganotosaurini include the presence of a postorbital process on the jugal with a wide base, and a derived femur with a weak fourth trochanter and a shallow broad extensor groove at the distal end.[9][7]
Tyrannotitan chubutensis lived during the Albian stage of the Early Cretaceous period, approximately 113 to 100 million years ago, in what is now the Cerro Castaño Member of the Cerro Barcino Formation in Chubut Province, Argentina. This region was part of Gondwana and featured a variety of environments, includingriver systems,floodplains, and semi-arid areas interspersed with scattered forests. The warm climate and abundant water sources, such as rivers and lakes, supported a diverse ecosystem that included largeherbivorous dinosaurs, smallertheropods, and other fauna.[10][11]
As anapex predator,Tyrannotitan likely played a significant role in shaping its ecosystem. Its diet primarily consisted of large herbivorous dinosaurs such asChubutisaurus and possibly juveniles or weaker individuals of massivesauropods likePatagotitan. These interactions highlight its position at the top of the food chain. Evidence suggests thatTyrannotitan may have been an active hunter, using its powerful bite and robust dentition to subdue prey, though it may also have scavenged opportunistically.[10][12][13]
Some studies propose thatTyrannotitan may have exhibitedadaptations forambush hunting near water sources. Its proximity to rivers and swamps not only provided cooling opportunities but also facilitated access to prey seeking refuge near these habitats. The possibility of social behavior remains speculative; however, tracksite evidence from other large theropods in Gondwana suggests that some degree of interaction or grouping behavior might have occurred.[12][14]
In their 2022 description of the large carcharodontosaurineMeraxes, Canale et al. placedTyrannotitan within the clade Giganotosaurini, along withMeraxes,Giganotosaurus, andMapusaurus. The results of theirphylogenetic analyses are shown in thecladogram below:[15]
In his 2024 review of theropod relationships, Cau found similar relationships forTyrannotitan. His results are shown below:[16]
| Carcharodontosauridae |
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