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Dicynodontia
Dicynodontia is an extinct clade of anomodonts, an extinct type of non-mammalian therapsid. Dicynodonts were herbivores that typically bore a pair of tusks, hence their name, which means 'two dog tooth'. Members of the group possessed a horny, typically toothless beak, unique amongst all synapsids. Dicynodonts first appeared in Southern Pangaea during the mid-Permian, ca. 270–260 million years ago, and became globally distributed and the dominant herbivorous animals in the Late Permian, ca. 260–252 Mya. They were devastated by the end-Permian mass extinction that wiped out most other therapsids ca. 252 Mya. They rebounded at beginning of the following Triassic, but subsequently declined and died out towards the end of that period. They were the most successful and diverse of the non-mammalian therapsids, with over 80-90 genera known, varying from rat-sized burrowers to elephant-sized browsers.
The dicynodont skull is highly specialised, light but strong, with the synapsid temporal openings at the rear of the skull greatly enlarged to accommodate larger jaw muscles. The front of the skull and the lower jaw are generally narrow and, in all but a number of primitive forms, toothless. Instead, the front of the mouth is equipped with a horny beak, as in turtles and ceratopsian dinosaurs. Food was processed by the retraction of the lower jaw when the mouth closed, producing a powerful shearing action, which would have enabled dicynodonts to cope with tough plant material. Dicynodonts typically had a pair of enlarged maxillary caniniform teeth, analogous to the tusks present in some living mammals. In the earliest genera, they were merely enlarged teeth, but in later forms they independently evolved into ever-growing teeth like mammal tusks multiple times. In some dicynodonts, the presence of tusks has been suggested to be sexually dimorphic. Some dicynodonts such as Stahleckeria lacked true tusks and instead bore tusk-like extensions on the side of the beak.
The body is short, strong and barrel-shaped, with strong limbs. In large genera (such as Dinodontosaurus) the hindlimbs were held erect, but the forelimbs bent at the elbow. Both the pectoral girdle and the ilium are large and strong. The tail is short.[citation needed]
Pentasauropus dicynodont tracks suggest that dicynodonts had fleshy pads on their feet. Mummified skin from specimens of Lystrosaurus in South Africa have numerous raised bumps.
Dicynodonts have long been suspected of being warm-blooded animals. Their bones are highly vascularised and possess Haversian canals, and their bodily proportions are conducive to heat preservation. In young specimens, the bones are so highly vascularised that they exhibit higher channel densities than most other therapsids. Yet, studies on Late Triassic dicynodont coprolites paradoxically showcase digestive patterns more typical of animals with slow metabolisms.
More recently, the discovery of hair remnants in Permian coprolites possibly vindicates the status of dicynodonts as endothermic animals. As these coprolites come from carnivorous species and digested dicynodont bones are abundant, it has been suggested that at least some of these hair remnants come from dicynodont prey. A new study using chemical analysis seemed to suggest that cynodonts and dicynodonts both developed warm blood independently before the Permian extinction.
A 2024 paper posited that rock art of a superficially walrus-like imaginary creature with downcurved tusks created by the San people of South Africa prior to 1835 may have been partly inspired by fossil dicynodont skulls which erode out of rocks in the area.
Dicynodonts have been known to science since the mid-1800s. The South African geologist Andrew Geddes Bain gave the first description of dicynodonts in 1845. At the time, Bain was a supervisor for the construction of military roads under the Corps of Royal Engineers and had found many reptilian fossils during his surveys of South Africa. Bain described these fossils in an 1845 letter published in Transactions of the Geological Society of London, calling them "bidentals" for their two prominent tusks. In that same year, the English paleontologist Richard Owen named two species of dicynodonts from South Africa: Dicynodon lacerticeps and Dicynodon bainii. Since Bain was preoccupied with the Corps of Royal Engineers, he wanted Owen to describe his fossils more extensively. Owen did not publish a description until 1876 in his Descriptive and Illustrated Catalogue of the Fossil Reptilia of South Africa in the Collection of the British Museum. By this time, many more dicynodonts had been described. In 1859, another important species called Ptychognathus declivis was named from South Africa. In the same year, Owen named the group Dicynodontia. In his Descriptive and Illustrated Catalogue, Owen honored Bain by erecting Bidentalia as a replacement name for his Dicynodontia. The name Bidentalia quickly fell out of use in the following years, replaced by popularity of Owen's Dicynodontia.
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Dicynodontia
Dicynodontia is an extinct clade of anomodonts, an extinct type of non-mammalian therapsid. Dicynodonts were herbivores that typically bore a pair of tusks, hence their name, which means 'two dog tooth'. Members of the group possessed a horny, typically toothless beak, unique amongst all synapsids. Dicynodonts first appeared in Southern Pangaea during the mid-Permian, ca. 270–260 million years ago, and became globally distributed and the dominant herbivorous animals in the Late Permian, ca. 260–252 Mya. They were devastated by the end-Permian mass extinction that wiped out most other therapsids ca. 252 Mya. They rebounded at beginning of the following Triassic, but subsequently declined and died out towards the end of that period. They were the most successful and diverse of the non-mammalian therapsids, with over 80-90 genera known, varying from rat-sized burrowers to elephant-sized browsers.
The dicynodont skull is highly specialised, light but strong, with the synapsid temporal openings at the rear of the skull greatly enlarged to accommodate larger jaw muscles. The front of the skull and the lower jaw are generally narrow and, in all but a number of primitive forms, toothless. Instead, the front of the mouth is equipped with a horny beak, as in turtles and ceratopsian dinosaurs. Food was processed by the retraction of the lower jaw when the mouth closed, producing a powerful shearing action, which would have enabled dicynodonts to cope with tough plant material. Dicynodonts typically had a pair of enlarged maxillary caniniform teeth, analogous to the tusks present in some living mammals. In the earliest genera, they were merely enlarged teeth, but in later forms they independently evolved into ever-growing teeth like mammal tusks multiple times. In some dicynodonts, the presence of tusks has been suggested to be sexually dimorphic. Some dicynodonts such as Stahleckeria lacked true tusks and instead bore tusk-like extensions on the side of the beak.
The body is short, strong and barrel-shaped, with strong limbs. In large genera (such as Dinodontosaurus) the hindlimbs were held erect, but the forelimbs bent at the elbow. Both the pectoral girdle and the ilium are large and strong. The tail is short.[citation needed]
Pentasauropus dicynodont tracks suggest that dicynodonts had fleshy pads on their feet. Mummified skin from specimens of Lystrosaurus in South Africa have numerous raised bumps.
Dicynodonts have long been suspected of being warm-blooded animals. Their bones are highly vascularised and possess Haversian canals, and their bodily proportions are conducive to heat preservation. In young specimens, the bones are so highly vascularised that they exhibit higher channel densities than most other therapsids. Yet, studies on Late Triassic dicynodont coprolites paradoxically showcase digestive patterns more typical of animals with slow metabolisms.
More recently, the discovery of hair remnants in Permian coprolites possibly vindicates the status of dicynodonts as endothermic animals. As these coprolites come from carnivorous species and digested dicynodont bones are abundant, it has been suggested that at least some of these hair remnants come from dicynodont prey. A new study using chemical analysis seemed to suggest that cynodonts and dicynodonts both developed warm blood independently before the Permian extinction.
A 2024 paper posited that rock art of a superficially walrus-like imaginary creature with downcurved tusks created by the San people of South Africa prior to 1835 may have been partly inspired by fossil dicynodont skulls which erode out of rocks in the area.
Dicynodonts have been known to science since the mid-1800s. The South African geologist Andrew Geddes Bain gave the first description of dicynodonts in 1845. At the time, Bain was a supervisor for the construction of military roads under the Corps of Royal Engineers and had found many reptilian fossils during his surveys of South Africa. Bain described these fossils in an 1845 letter published in Transactions of the Geological Society of London, calling them "bidentals" for their two prominent tusks. In that same year, the English paleontologist Richard Owen named two species of dicynodonts from South Africa: Dicynodon lacerticeps and Dicynodon bainii. Since Bain was preoccupied with the Corps of Royal Engineers, he wanted Owen to describe his fossils more extensively. Owen did not publish a description until 1876 in his Descriptive and Illustrated Catalogue of the Fossil Reptilia of South Africa in the Collection of the British Museum. By this time, many more dicynodonts had been described. In 1859, another important species called Ptychognathus declivis was named from South Africa. In the same year, Owen named the group Dicynodontia. In his Descriptive and Illustrated Catalogue, Owen honored Bain by erecting Bidentalia as a replacement name for his Dicynodontia. The name Bidentalia quickly fell out of use in the following years, replaced by popularity of Owen's Dicynodontia.