Gastralia

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Crocodiles have the abdominal ribs modified into gastralia Crocodilelyd5.png
Crocodiles have the abdominal ribs modified into gastralia
Tyrannosaurus gastralia Tyrannosaurus gastralia.jpg
Tyrannosaurus gastralia

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.

Contents

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]

Pathology

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 [6] specimen MOR 693 also had pathological gastralia. [7] The left scapula and fibula of an Allosaurus fragilis specimen catalogued as USNM 4734 are both pathological, both probably due to healed fractures. [8]

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. [8]

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. [8]

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. [8]

The unidentified tyrannosaurid specimen TMP97.12.229 had a fractured and healed gastralium. [8]

Related Research Articles

<i>Allosaurus</i> Extinct genus of carnosaurian theropod dinosaur

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. As one of the first well-known theropod dinosaurs, it has long attracted attention outside of paleontological circles.

<i>Gorgosaurus</i> Genus of tyrannosaur dinosaur

Gorgosaurus is a genus of tyrannosaurid theropod dinosaur that lived in western North America during the Late Cretaceous Period (Campanian), between about 76.6 and 75.1 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.

<i>Ceratosaurus</i> Genus of theropod dinosaur from the Late Jurassic period

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.

<i>Acrocanthosaurus</i> Genus of carcharodontosaurid dinosaur from the Early Cretaceous

Acrocanthosaurus is a genus of carcharodontosaurid dinosaur that existed in what is now North America during the Aptian and early Albian stages of the Early Cretaceous, from 113 to 110 million years ago. Like most dinosaur genera, Acrocanthosaurus contains only a single species, A. atokensis. It had a continent-wide range, with fossil remains known from the U.S. states of Oklahoma, Texas, and Wyoming in the west, and Maryland in the east.

<i>Torvosaurus</i> Megalosaurid theropod dinosaur genus from Late Jurassic Period

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.

<i>Deinocheirus</i> Genus of theropod dinosaurs

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.

<span class="mw-page-title-main">Allosauridae</span> Extinct family of theropod dinosaurs

Allosauridae is a 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.

<i>Elaphrosaurus</i> Ceratosaurian theropod dinosaur genus from the Late Jurassic Period

Elaphrosaurus is a genus of ceratosaurian theropod dinosaur that lived approximately 154 to 150 million years ago during the Late Jurassic Period in what is now Tanzania in Africa. Elaphrosaurus was a medium-sized but lightly built member of the group that could grow up to 6.2 m (20 ft) long. Morphologically, this dinosaur is significant in two ways. Firstly, it has a relatively long body but is very shallow-chested for a theropod of its size. Secondly, it has very short hindlimbs in comparison with its body. Phylogenetic analyses indicate that this genus is likely a ceratosaur. Earlier suggestions that it is a late surviving coelophysoid have been examined but generally dismissed. Elaphrosaurus is currently believed to be a very close relative of Limusaurus, an unusual beaked ceratosaurian which may have been either herbivorous or omnivorous.

<i>Epanterias</i> Extinct genus of dinosaurs

Epanterias is a dubious genus of theropod dinosaur from the Kimmeridgian-Tithonian age Upper Jurassic upper Morrison Formation of Garden Park, Colorado. It was described by Edward Drinker Cope in 1878. The type species is Epanterias amplexus. This genus is based on what is now AMNH 5767, parts of three vertebrae, a coracoid, and a metatarsal. Although Cope thought it was a sauropod, it was later shown to be a theropod. Gregory S. Paul reassessed the material as pertaining to a large species of Allosaurus in 1988. Other authors have gone further and considered E. amplexus as simply a large individual of Allosaurus fragilis. In 2010, Gregory S. Paul and Kenneth Carpenter noted that the E. amplexus specimen comes from higher in the Morrison Formation than the type specimen of Allosaurus fragilis, and is therefore "probably a different taxon". They also considered its holotype specimen not diagnostic and classified it as a nomen dubium.

<i>Dinheirosaurus</i> Genus of reptiles (fossil)

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.

<i>Majungasaurus</i> Abelisaurid theropod dinosaur from the Late Cretaceous period

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.

<i>Tanycolagreus</i> Extinct genus of reptiles

Tanycolagreus is a genus of coelurosaurian theropod from the Late Jurassic of North America.

<i>Marshosaurus</i> Extinct genus of dinosaurs

Marshosaurus is a genus of medium-sized carnivorous theropod dinosaur, belonging to the Megalosauroidea, from the Late Jurassic Morrison Formation of Utah and possibly Colorado.

<i>Lourinhanosaurus</i> Extinct genus of dinosaurs

Lourinhanosaurus was a genus of carnivorous theropod dinosaur that lived during the Late Jurassic Period (Kimmeridgian/Tithonian) in Portugal. It is one of many large predators discovered at the Lourinhã Formation and probably competed with coeval Torvosaurus gurneyi, Allosaurus europaeus, and Ceratosaurus.

<i>Poekilopleuron</i> Extinct genus of dinosaurs

Poekilopleuron is a genus of tetanuran 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.

<i>Spinophorosaurus</i> Middle Jurassic genus of sauropod dinosaur

Spinophorosaurus is a genus of sauropod dinosaur that lived in what is now Niger during the Middle Jurassic period. The first two specimens were excavated in the 2000s by German and Spanish teams under difficult conditions. The skeletons were brought to Europe and digitally replicated, making Spinophorosaurus the first sauropod to have its skeleton 3D printed, and were to be returned to Niger in the future. Together, the two specimens represented most of the skeleton of the genus, and one of the most completely known basal sauropods of its time and place. The first skeleton was made the holotype specimen of the new genus and species Spinophorosaurus nigerensis in 2009; the generic name refers to what was initially thought to be spiked osteoderms, and the specific name refers to where it was found. A juvenile sauropod from the same area was later assigned to the genus.

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.

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.

<i>Phuwiangvenator</i> Extinct genus of dinosaurs

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.

References

  1. Kardong KV (2002). Vertebrates: Comparative Anatomy, Function, Evolution (3rd ed.). New York: McGraw-Hill. pp.  291–293. ISBN   0-07-290956-0.
  2. 1 2 3 4 Claessens LP (March 2004). "Dinosaur gastralia: origin, morphology, and function" (PDF). Journal of Vertebrate Paleontology. 24 (1): 89–106. doi:10.1671/A1116-8. S2CID   53318713.
  3. Tschopp E, Mateus O (March 2013). "Clavicles, interclavicles, gastralia, and sternal ribs in sauropod dinosaurs: new reports from diplodocidae and their morphological, functional and evolutionary implications". Journal of Anatomy. 222 (3): 321–40. doi:10.1111/joa.12012. PMC   3582252 . PMID   23190365.
  4. Radermacher VJ, Fernandez V, Schachner ER, Butler RJ, Bordy EM, Naylor Hudgins M, et al. (July 2021). Long JA, Perry GH, Spencer M (eds.). "A new Heterodontosaurus specimen elucidates the unique ventilatory macroevolution of ornithischian dinosaurs". eLife. 10: e66036. doi: 10.7554/eLife.66036 . PMC   8260226 . PMID   34225841.
  5. "A Fresh Science Makeover for SUE". 30 November 2018. Retrieved 17 December 2021.
  6. Chure DJ, Loewen MA (2020). "Cranial anatomy of Allosaurus jimmadseni, a new species from the lower part of the Morrison Formation (Upper Jurassic) of Western North America". PeerJ. 8: e7803. doi: 10.7717/peerj.7803 . PMC   6984342 . PMID   32002317.
  7. Hanna RR (March 2002). "Multiple injury and infection in a sub-adult theropod dinosaur Allosaurus fragilis with comparisons to allosaur pathology in the Cleveland-Lloyd Dinosaur Quarry collection". Journal of Vertebrate Paleontology. 22 (1): 76–90. doi:10.1671/0272-4634(2002)022[0076:MIAIIA]2.0.CO;2. S2CID   85654858.
  8. 1 2 3 4 5 Molnar RE (2001). "Theropod paleopathology: a literature survey". In Tanke DH, Carpenter K (eds.). Mesozoic Vertebrate Life. Indiana University Press. pp. 337–363.