Gastralia (sg.: gastralium) are dermal bones found in the ventral body wall of modern crocodilians and tuatara, and many prehistoric tetrapods. They are found between the sternum and pelvis, and do not articulate with the vertebrae. In these reptiles, gastralia provide support for the abdomen and attachment sites for abdominal muscles.
The possession of gastralia may be ancestral for Tetrapoda and were possibly derived from the ventral scales found in animals like rhipidistians, labyrinthodonts, and Acanthostega , and may be related to ventral elements of turtle plastrons. [1] [2] Similar, but not homologous cartilagenous elements, are found in the ventral body walls of lizards and anurans. These structures have been referred to as inscriptional ribs, [2] based on their alleged association with the inscriptiones tendinae (the tendons that form the six pack in humans). However, the terminology for these gastral-like structures remains confused. Both types, along with sternal ribs (ossified costal cartilages), have been referred to as abdominal ribs, a term with limited usefulness that should be avoided. [2] Gastralia are also present in a variety of extinct animals, including theropod and prosauropod dinosaurs, pterosaurs, plesiosaurs, choristoderes and some primitive pelycosaurs. In dinosaurs, the elements articulate with each other in a sort of zig-zag along the midline and may have aided in respiration. [2] Gastralia are known to be present in primitive ornithischian and sauropodomorph dinosaurs. However gastralia are only known from heterodontosaurid ornithschians, and gastralia are lost in eusauropodan sauropods. [3] [4]
Discoveries about how the gastralia fit together in the skeleton of Sue the T. rex have led to an understanding that Tyrannosaurus bodies were more barrel-chested – and heavier – than previously thought. [5]
The term "gastralia" was proposed by Georg Baur in 1898. [6] They had previously been termed "abdominal ribs", [7] but because the term "abdominal ribs" has been applied to various structures, and the gastralia are not true ribs, this is not considered an appopriate term. [6] [2]
In turtles, where the gastralia are incorporated into the plastron, each pair of gastralia gets a distinct name: the hyoplastra, hypoplastra, xiphiplastra, and in some taxa the mesoplastra. [8]
Gastralia were ancestrally present in amniotes, but have been lost in many groups. Among extant taxa, they are only present in crocodylians and the tuatara, and in modified form as part of the plastron of turtles. [2] Gastralia are rarely preserved in therapsids, but have been identified in some dinocephalians and gorgonopsians and several anomodonts. However, they were probably genuinely absent in some dicynodonts, therocephalians, and cynodonts. [9] Most ornithischian dinosaurs lacked gastralia, but heterodontosaurids, one of the earliest-branching lineages of ornithischians, retained them. [10] Sauropods have been considered to lack gastralia. [2] [11] Elements interpreted as gastralia have been rarely found in sauropods, [12] but it has been argued that these elements are more convincingly interpreted as sternal ribs. [11] Modern birds lack gastralia, but they were present in early lineages of birds, as in other theropods. [13]
The Allosaurus fragilis specimen USNM 8367 contained several gastralia which preserve evidence of healed fractures near their middle. Some of the fractures were poorly healed and "formed pseudoarthroses." An apparent subadult male Allosaurus fragilis was reported by Laws to have extensive pathologies. The possible subadult A. jimmadseni [14] specimen MOR 693 also had pathological gastralia. [15] The left scapula and fibula of an Allosaurus fragilis specimen catalogued as USNM 4734 are both pathological, both probably due to healed fractures. [16]
The holotype of Neovenator salerii had many pathologies, including pseudoarthrotic gastralia and a deviation to the right of the third and fourth neural spines of the neck vertebrae. [16]
An immature dromaeosaurid specimen (which had not been described in the scientific literature as of 2001) from Tugrugeen Shireh was observed to have a "bifurcated" gastralium. [16]
In the Gorgosaurus libratus holotype (NMC 2120) the 13th and 14th gastralia have healed fractures. Another G. libratus specimen catalogued as TMP94.12.602 bears multiple pathologies, including a pseudoarthortic gastralium. [16]
The unidentified tyrannosaurid specimen TMP97.12.229 had a fractured and healed gastralium. [16]
Allosaurus is an extinct genus of large carnosaurian theropod dinosaur that lived 155 to 145 million years ago during the Late Jurassic period. The name "Allosaurus" means "different lizard", alluding to its unique concave vertebrae. It is derived from the Greek words ἄλλος and σαῦρος. The first fossil remains that could definitively be ascribed to this genus were described in 1877 by famed paleontologist Othniel Charles Marsh. The genus has a very complicated taxonomy and includes at least three valid species, the best known of which is A. fragilis. The bulk of Allosaurus remains have come from North America's Morrison Formation, with material also known from the Lourinhã Formation in Portugal. It was known for over half of the 20th century as Antrodemus, but a study of the abundant remains from the Cleveland-Lloyd Dinosaur Quarry returned the name "Allosaurus" to prominence. As one of the first well-known theropod dinosaurs, it has long attracted attention outside of paleontological circles.
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.
Ceratosaurus was a carnivorous theropod dinosaur that lived in the Late Jurassic period. The genus was first described in 1884 by American paleontologist Othniel Charles Marsh based on a nearly complete skeleton discovered in Garden Park, Colorado, in rocks belonging to the Morrison Formation. The type species is Ceratosaurus nasicornis.
Torvosaurus is a genus of large megalosaurine theropod dinosaur that lived approximately 165 to 148 million years ago during the Callovian to Tithonian ages of the late Middle and Late Jurassic period in what is now Colorado, Portugal, Germany, and possibly England, Spain, Tanzania, and Uruguay. It contains two currently recognized species, Torvosaurus tanneri and Torvosaurus gurneyi, plus a third unnamed species from Germany.
Deinocheirus is a genus of large ornithomimosaur that lived during the Late Cretaceous around 70 million years ago. In 1965, a pair of large arms, shoulder girdles, and a few other bones of a new dinosaur were first discovered in the Nemegt Formation of Mongolia. In 1970, this specimen became the holotype of the only species within the genus, Deinocheirus mirificus; the genus name is Greek for "horrible hand". No further remains were discovered for almost fifty years, and its nature remained a mystery. Two more complete specimens were described in 2014, which shed light on many aspects of the animal. Parts of these new specimens had been looted from Mongolia some years before, but were repatriated in 2014.
Abrictosaurus is a genus of heterodontosaurid dinosaur that lived during the Early Jurassic in what is now in parts of southern Africa such as Lesotho and South Africa. It was a bipedal herbivore or omnivore and was one of the most basal heterodontosaurids. It was approximately 1.2 metres (3.9 ft) long and weighed between 0.68 and 3 kilograms.
Allosauridae is an extinct family of medium to large bipedal, carnivorous allosauroid theropod dinosaurs from the Late Jurassic. Allosauridae is a fairly old taxonomic group, having been first named by the American paleontologist Othniel Charles Marsh in 1878. Allosaurids are characterized by an astragalus with a restriction of the ascending process to the lateral part of the bone, a larger medial than lateral condyle, and a horizontal groove across the face of the condyles.
Heterodontosaurus is a genus of heterodontosaurid dinosaur that lived during the Early Jurassic, 200–190 million years ago. Its only known member species, Heterodontosaurus tucki, was named in 1962 based on a skull discovered in South Africa. The genus name means "different toothed lizard", in reference to its unusual, heterodont dentition; the specific name honours G. C. Tuck, who supported the discoverers. Further specimens have since been found, including an almost complete skeleton in 1966.
Saurophaganax is a genus of large allosauroid dinosaur from the Morrison Formation of Late Jurassic Oklahoma, United States. Some paleontologists consider it to be a junior synonym and species of Allosaurus. Saurophaganax represents a very large Morrison allosauroid characterized by horizontal laminae at the bases of the dorsal neural spines above the transverse processes, and "meat-chopper" chevrons. It was the largest terrestrial carnivore of North America during the Late Jurassic, reaching 10.5 metres (34 ft) in length and 2.7–3.8 metric tons in body mass.
Dinheirosaurus is a genus of diplodocid sauropod dinosaur that is known from fossils uncovered in modern-day Portugal. It may represent a species of Supersaurus. The only species is Dinheirosaurus lourinhanensis, first described by José Bonaparte and Octávio Mateus in 1999 for vertebrae and some other material from the Lourinhã Formation. Although the precise age of the formation is not known, it can be dated around the early Tithonian of the Late Jurassic.
Majungasaurus is a genus of abelisaurid theropod dinosaur that lived in Madagascar from 70 to 66 million years ago, at the end of the Cretaceous Period, making it one of the last-known non-avian dinosaurs that went extinct during the Cretaceous–Paleogene extinction event. The genus contains a single species, Majungasaurus crenatissimus. This dinosaur is also called Majungatholus, a name which is considered a junior synonym of Majungasaurus.
Marshosaurus is a genus of medium-sized carnivorous theropod dinosaur, belonging to the family Piatnitzkysauridae, from the Late Jurassic Morrison Formation of Utah and possibly Colorado.
Poekilopleuron is a genus of carnosaurian theropod dinosaur, which lived during the middle Bathonian of the Jurassic, about 168 to 166 million years ago. The genus has been used under many different spelling variants, although only one, Poekilopleuron, is valid. The type species is P. bucklandii, named after William Buckland, and many junior synonyms of it have also been erected. Little material is currently known, as the holotype was destroyed in World War II, although many casts of the material still exist.
The turtle shell is a shield for the ventral and dorsal parts of turtles, completely enclosing all the vital organs of the turtle and in some cases even the head. It is constructed of modified bony elements such as the ribs, parts of the pelvis and other bones found in most reptiles. The bone of the shell consists of both skeletal and dermal bone, showing that the complete enclosure of the shell likely evolved by including dermal armor into the rib cage.
Theropod paleopathology is the study of injury and disease in theropod dinosaurs. In 2001, Ralph E. Molnar published a survey of pathologies in theropod dinosaur bone that uncovered pathological features in 21 genera from 10 theropod families. Pathologies have been seen on most theropod body parts, with the most common sites of preserved injury and disease being the ribs and tail vertebrae. The least common sites of preserved pathology are the weight-bearing bones like the tibia, femur and sacrum. Most pathologies preserved in theropod fossils are the remains of injuries, but infections and congenital deformities have also been documented. Pathologies are less frequently documented in small theropods, although this may simply be because the larger bones of correspondingly larger animals would be more likely to fossilize in the first place.
Pegomastax is a genus of heterodontosaurid dinosaur that lived during the Early Jurassic of South Africa. The only known specimen was discovered in a 1966–1967 expedition in Transkei District of Cape Province, but was not described until 2012 when Paul Sereno named it as the new taxon Pegomastax africana. The genus name is derived from the Greek for "strong jaw", and the species name describes the provenance of Africa; it was originally spelled africanus, was corrected to africana to align with the gender of the genus name.
This glossary explains technical terms commonly employed in the description of dinosaur body fossils. Besides dinosaur-specific terms, it covers terms with wider usage, when these are of central importance in the study of dinosaurs or when their discussion in the context of dinosaurs is beneficial. The glossary does not cover ichnological and bone histological terms, nor does it cover measurements.
Phuwiangvenator is an extinct genus of megaraptoran theropod that lived during the Early Cretaceous period in what is now Thailand. It contains only the type species, P. yaemniyomi. The generic name of Phuwiangvenator comes from the Phu Wiang mountains, where the holotype was discovered, and the Latin word "venator" meaning hunter. The specific name, "yaemniyomi", is in honor of Sudham Yaemniyom, who was a historical paleontologist from Thailand and the first person to discover fossils there.
Ardetosaurus is an extinct genus of diplodocid sauropod dinosaurs from the Late Jurassic (Kimmeridgian) Morrison Formation of northern Wyoming, United States. The genus contains a single species, Ardetosaurus viator. It was first described in 2024 on the basis of a partial articulated skeleton, including vertebrae from the neck, back, and tail, hip bones, and part of the left hindlimb. The genus is a member of the Diplodocinae, a subfamily of large long-necked dinosaurs with whiplike tails. Ardetosaurus represents one of many distinct sauropod taxa that coexisted in this formation.