Majungasaurinae Temporal range: Late Cretaceous, | |
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Majungasaurus crenatissimus mounted skeleton, Stony Brook University | |
Scientific classification | |
Domain: | Eukaryota |
Kingdom: | Animalia |
Phylum: | Chordata |
Clade: | Dinosauria |
Clade: | Saurischia |
Clade: | Theropoda |
Family: | † Abelisauridae |
Subfamily: | † Majungasaurinae Tortosa et al., 2014 |
Type species | |
† Majungasaurus crenatissimus | |
Subgroups | |
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Synonyms | |
Majungasaurini Tortosa et al., 2014 vide Delcourt, 2018 Contents |
Majungasaurinae (after Majungasaurus, itself named after the city of Mahajanga in Madagascar) is a subfamily of large carnivorous theropods from the Upper Cretaceous, found in Madagascar, India, and France. It is a subgroup within the theropod family Abelisauridae, a Gondwanan clade known for their thick and often horned skulls and vestigial arms. The two subfamilies of Abelisauridae are Carnotaurinae, best known from the South American Carnotaurus , and Majungasaurinae, consisting of Madagascar’s Majungasaurus and its closest relatives. Their ancestors emerged in the Middle Jurassic, and the clade lasted until the Upper Cretaceous.
The majungasaurines were mid-sized, bipedal predators, but relatively slow moving. Their stout legs were built for striding, not running. They had tall, deep heads with powerful jaws, but small forearms without carpals in the wrists. Because of their slow gait and small arms, they likely preyed upon the larger, slower sauropods rather than the smaller, faster ornithopods. Their ancestors lived on a unified southern continent, Gondwana, in the Early Cretaceous, but as the land mass divided they became distinct from their South American cousins, and eventually from each other.
The abelisaurids all possess distinct, vestigial, and immobile forelimbs, with highly reduced manual phalanges. [2] Carnotaurus and Majungasaurus are closely related but distinguish by several skeletal features. Carnotaurus has eleven dorsal vertebrae but Majungasaurus has thirteen. [3] Carnotaurus has short dentary bones and an almost vertical ramus, while that of Majungasaurus curved backward and had notable caudal projections.[ citation needed ] Majungasaurines also have low, wide antorbital fenestrae, a wide triangular plate posterior to the parietal, two holes for a cerebral vein by the sagittal crest, and a wide groove on the occipital condyle. [4] These differences are important because derived abelisaurids are classed as either majungasaurines or carnotaurines based on their synapomorphies.
The first majungasaurine to be uncovered was Majungasaurus, discovered in Madagascar in 1896, however was named as a species of Megalosaurus . [5] Indosaurus and Indosuchus were both discovered in India and described in 1933 by Charles Alfred Matley and Friedrich von Huene as allosaurids. The name Majungasaurus was erected by René Lavocat in 1955 for some teeth and a dentary which showed that the animal was distinct from Megalosaurus. In 1996, a species, Majungatholus was erected for a supposed pachycephalosaurid from Madagascar, however this turned out to belong to a specimen of Majungasaurus. in 1991 that paleontologist Jose Bonaparte theorized that these and many other theropods belonged to the same family, the abelisaurids. [6] Tortosa et al., 2014 created a new subfamily of abelisaurids, the Majungasaurinae, which unified abelisaurids from Europe, Madagascar and India into a single clade. [4]
The clade Majungasaurinae is relatively new, proposed in March 2014 by paleontologist Thierry Tortosa and colleagues in the description of Arcovenator. It is defined as all abelisaurids more closely related to Majungasaurus than to Carnotaurus. The cladogram below shows the result of the study's phylogenetic analysis. [8]
Abelisauridae |
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The following cladogram is a consensus tree of the latest phylogenies from 2018. [9] Only the phylogenies for Abelisauridae is depicted here. Two smaller clades were erected within majungasaurinae. One of them encompassed the more robust abelisaurids from Madagascar and India with another clade comprising Rahiolisaurus and Dahalokely.
In the 2021 description of Llukalkan , both Rahiolisaurus and Dahalokely were placed outside of majungasaurinae as basal brachyrostrans. It agreed with the existence of a clade comprising Majungasaurus, Indosaurus and Rajasaurus but also found Arcovenator and Genusaurus to form a sister taxon relationship. [10]
The majungasaurines and their carnotaurine sister group emerged in what is now South America. From there they spread to the rest of Gondwana: modern Africa and India, and presumably Australia and Antarctica as well. [11] Fragmentary evidence of abelisaurs in southern France indicates they may have spread into Europe as well, but the relationship of these species to the rest of Majungasaurinae is not well established. [12]
Like all abelisaurs, the majungasaurines were carnivorous and had bulbous teeth, short heads, and strong necks. This meant that their wide jaws were very powerful, and could crush their prey’s trachea or vertebrae once they bit down. [13] Majungasaurus is known to have preyed upon medium-sized sauropods such as Rapetosaurus , and its teeth marks have been found on the ribs of other Majungasaurus. Whether it actively hunted members of its own species or merely cannibalized their scavenged remains is unknown. This behavior has not been observed in any other majungasaurines. [14]
Carnotaurus is a genus of theropod dinosaur that lived in South America during the Late Cretaceous period, probably sometime between 72 and 69 million years ago. The only species is Carnotaurus sastrei. Known from a single well-preserved skeleton, it is one of the best-understood theropods from the Southern Hemisphere. The skeleton, found in 1984, was uncovered in the Chubut Province of Argentina from rocks of the La Colonia Formation. Carnotaurus is a derived member of the Abelisauridae, a group of large theropods that occupied the large predatorial niche in the southern landmasses of Gondwana during the late Cretaceous. Within the Abelisauridae, the genus is often considered a member of the Brachyrostra, a clade of short-snouted forms restricted to South America.
Ceratosaurs are members of the clade Ceratosauria, a group of dinosaurs defined as all theropods sharing a more recent common ancestor with Ceratosaurus than with birds. The oldest known ceratosaur, Saltriovenator, dates to the earliest part of the Jurassic, around 199 million years ago. Ceratosauria includes three major clades: Ceratosauridae, Noasauridae, and Abelisauridae, found primarily in the Southern Hemisphere. Originally, Ceratosauria included the above dinosaurs plus the Late Triassic to Early Jurassic Coelophysoidea and Dilophosauridae, implying a much earlier divergence of ceratosaurs from other theropods. However, most recent studies have shown that coelophysoids and dilophosaurids do not form a natural group with other ceratosaurs, and are excluded from this group.
Rajasaurus is a genus of carnivorous abelisaurid theropod dinosaur from the Late Cretaceous of India, containing one species: Rajasaurus narmadensis. The bones were excavated from the Lameta Formation in the Gujarat state of Western India, probably inhabiting what is now the Narmada River Valley. It was formally described by palaeontologist Jeffrey A. Wilson and colleagues in 2003 based on a partial skeleton comprising the braincase, spine, hip bone, legs, and tail–a first for an Indian theropod. The dinosaur likely measured 6.6 metres (22 ft), and had a single horn on the forehead which was probably used for display and head-butting. Like other abelisaurids, Rajasaurus was probably an ambush predator.
Abelisaurus is a genus of predatory abelisaurid theropod dinosaur alive during the Late Cretaceous Period (Campanian) of what is now South America. It was a bipedal carnivore that probably reached about 7.4 metres in length, although this is uncertain as it is known from only one partial skull.
Rugops is a monospecific genus of basal abelisaurid theropod dinosaur from Niger that lived during the Late Cretaceous period in what is now the Echkar Formation. The type and only species, Rugops primus, is known only from a partial skull. It was named and described in 2004 by Paul Sereno, Jeffery Wilson and Jack Conrad. Rugops has an estimated length of 4.4–5.3 metres (14–17 ft) and weight of 410 kilograms (900 lb). The top of its skull bears several pits which correlates with overlaying scale and the front of the snout would have had an armour-like dermis.
Abelisauridae is a family of ceratosaurian theropod dinosaurs. Abelisaurids thrived during the Cretaceous period, on the ancient southern supercontinent of Gondwana, and today their fossil remains are found on the modern continents of Africa and South America, as well as on the Indian subcontinent and the island of Madagascar. Isolated teeth were found in the Late Jurassic of Portugal, and the Late Cretaceous genera Tarascosaurus, Arcovenator and Caletodraco have been described in France. Abelisaurids possibly first appeared during the Jurassic period based on fossil records, and some genera survived until the end of the Mesozoic era, around 66 million years ago.
Aucasaurus is a genus of medium-sized abelisaurid theropod dinosaur from Argentina that lived during the Late Cretaceous of the Anacleto Formation. It was smaller than the related Carnotaurus, although more derived in some ways, such as its extremely reduced arms and almost total lack of fingers. The type skeleton is complete to the thirteenth caudal vertebra, and so is relatively well understood, and is the most complete abelisaurid yet described. However, the skull is damaged, causing some paleontologists to speculate that it was involved in a fight prior to death.
Tarascosaurus is a genus of abelisaurid theropod dinosaur from Late Cretaceous of France. It was a relatively small theropod measuring 2.5–3 metres (8.2–9.8 ft) long.
Ilokelesia is an extinct genus of abelisaurid theropod, preserved in the layers of the earliest Late Cretaceous of the Huincul Formation, Neuquén Group, located near Plaza Huincul, Neuquén Province, Argentina. The specimen, consisting of very fragmentary elements of the skull and the axial and appendicular skeleton, was described by Rodolfo Coria and Leonardo Salgado in late 1998.
Quilmesaurus is a genus of carnivorous abelisaurid theropod dinosaur from the Patagonian Upper Cretaceous of Argentina. It was a member of Abelisauridae, closely related to genera such as Carnotaurus. The only known remains of this genus are leg bones which share certain similarities to a variety of abelisaurids. However, these bones lack unique features, which may render Quilmesaurus a nomen vanum.
Indosaurus is a genus of carnivorous theropod dinosaur that lived in what is now India, about 69 to 66 million years ago during the Maastrichtian division of the Late Cretaceous.
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.
Ekrixinatosaurus is a genus of abelisaurid theropod which lived approximately 100 to 97 million years ago during the Late Cretaceous period. Its fossils have been found in Argentina. Only one species is currently recognized, Ekrixinatosaurus novasi, from which the specific name honors of Dr. Fernando Novas for his contributions to the study of abelisaurid theropods, while the genus name refers to the dynamiting of the holotype specimen. It was a large abelisaur, measuring between 6.5 and 8 m in length and weighing 800 kg (1,800 lb).
Brachyrostra is a clade within the theropod dinosaur family Abelisauridae. It includes the famous genera Carnotaurus, Abelisaurus, Aucasaurus as well as their close relatives from the Cretaceous Period of Argentina and Brazil plus Caletodraco from France. The group was first proposed in an analysis conducted by Juan Canale and colleagues in 2008. They found that all South American abelisaurids described up to that point grouped together as a sub-clade of Abelisauridae, which they named based on the relatively unusual shape of their skulls. They defined the clade Brachyrostra as "all the abelisaurids more closely related to Carnotaurus sastrei than to Majungasaurus crenatissimus."
Rahiolisaurus is a genus of abelisaurid theropod dinosaur which existed in India during the Late Cretaceous period. It was described in 2010, based on fossils recovered from the Lameta Formation in the Indian state of Gujarat. These fossils include elements from at least seven different individuals and are believed to have been from the Maastrichtian stage, sometime between 70 and 66 million years ago, making it one of the last non-avian dinosaurs known in the fossil record. Despite representing a variety of different growth stages, all recovered fossils from the locality indicate a single species, the type species Rahiolisaurus gujaratensis.
Arcovenator is an extinct genus of abelisaurid theropod dinosaurs hailing from the Late Cretaceous of France and possibly Spain. The type and only described species is Arcovenator escotae.
This timeline of ceratosaur research is a chronological listing of events in the history of paleontology focused on the ceratosaurs, a group of relatively primitive, often horned, predatory theropod dinosaurs that became the apex predators of the southern hemisphere during the Late Cretaceous. The nature and taxonomic composition of the Ceratosauria has been controversial since the group was first distinguished in the late 19th century. In 1884 Othniel Charles Marsh described the new genus and species Ceratosaurus nasicornis from the Late Jurassic Morrison Formation of the western United States. He felt that it belonged in a new family that he called the Ceratosauridae. He created the new taxon Ceratosauria to include both the Ceratosauridae and the ostrich-like ornithomimids. The idea of the Ceratosauria was soon contested, however. Later that same decade both Lydekker and Marsh's hated rival Edward Drinker Cope argued that the taxon was invalid.
Viavenator is a genus of carnivorous abelisaurid theropod dinosaur discovered in Argentina's Bajo de la Carpa Formation. It coexisted with the megaraptoran Tratayenia rosalesi.
Chenanisaurus is a genus of predatory abelisaurid dinosaur, with a single known species C. barbaricus. It comes from the upper Maastrichtian phosphates of the Ouled Abdoun Basin in Morocco, North Africa. The animal is known from a holotype, consisting of a partial jaw bone, and several isolated teeth found in the same beds. Chenanisaurus is one of the largest members of the Abelisauridae, and one of the last, being a contemporary of the North American Tyrannosaurus. It would have been among the dinosaur species wiped out by the Chicxulub asteroid impact and the Cretaceous-Paleogene mass extinction that followed.
Tralkasaurus is a genus of abelisaurid dinosaur from the Huincul Formation from Río Negro Province in Argentina. The type and only species is Tralkasaurus cuyi, named in 2020 by Mauricio Cerroni and colleagues based on an incomplete skeleton. A medium-sized abelisaurid, Tralkasaurus exhibits a conflicting blend of characteristics found among the early-diverging abelisauroids with others that characterize the highly specialized clade Brachyrostra, and thus its position within the clade is poorly-resolved.