Venkatasuchus Temporal range: Late Triassic | |
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Life restoration of Venkatasuchus armatus | |
Scientific classification | |
Domain: | Eukaryota |
Kingdom: | Animalia |
Phylum: | Chordata |
Class: | Reptilia |
Clade: | Archosauria |
Clade: | Pseudosuchia |
Order: | † Aetosauria |
Family: | † Stagonolepididae |
Tribe: | † Paratypothoracini |
Genus: | † Venkatasuchus Haldar, Ray & Bandyopadhyay, 2023 |
Species: | †V. armatum |
Binomial name | |
†Venkatasuchus armatum Haldar, Ray & Bandyopadhyay, 2023 | |
Venkatasuchus is an extinct genus of aetosaur from the Late Triassic Dharmaram Formation of India. It was described in 2023 on the basis of a series of associated osteoderms that formed the paramedian and lateral armour. Based on the osteoderms the carapace of Venkatasuchus was disc-shaped and very wide, with curved, horn-like elements along its sides. Phylogenetic analysis indicates that Venkatasuchus belonged to the subfamily Typothoracinae and more specifically the clade Paratypothoracini, where it is recovered as the sister taxon to Kocurypelta . Venkatasuchus is among the few aetosaurs recovered from the region that would later become Gondwana and lends credence to the idea that late Triassic India represented a connective hub between Laurasian and Gondwanan fauna. The genus is monotypic, meaning it only includes a single species, Venkatasuchus armatum.
Venkatasuchus is known from a series of osteoderms that have been recovered from the Late Triassic Lower Dharmaram Formation of India, more specifically from a locality near the village of Rampur within India's Adilabad district. The holotype (ISIR267/1–7) consists of eight associated pieces of bone of the paramedian armour, the armour that is placed along the midline of the animal's back, as well as the associated lateral osteoderms that attach to the sides of the former. In addition to the holotype set of bones, an isolated osteoderm (ISIR286) has also been recovered and referred to the genus based on its shared anatomy. However, there are some differences between the isolated element and the type material. Seeing as these differences may be related to age, sex or simple intraspecific variation, it is currently believed that ISIR286 belonged to a different individual. [1]
The genus was named in honor of N. Venkata Raja Reddy, an enthusiast who helped with the discovery of fossils in the Pranhita-Godavari Basin. The second part of the name utilizes the Greek suffix "suchus", which is derived from the Egyptian deity Sobek and translates to "crocodile". The species name "armatum" simply means armoured. [1]
Although little material of Venkatasuchus is known, it can be readily distinguished from other aetosaurs by the combination of features present on its osteoderms. Though only few traits observed in Venkatasuchus are deemed unique to this taxon, its the specific combination of features that sets it apart from its relatives.
The anterior bar of the osteoderms, the front-most section, is thick and weakly raised, taking up around 36% of the length of the element. A raised anterior bar is a trait that is almost universal among aetosaurs, yet absent in Desmatosuchus . The anterior bar also features a straight anteriomedial margin which is considered an autapomorphy, a derived trait not seen in any other members of the group. More broadly the margin of the entire medial section of the anterior bar is straight, but this is also shared by Paratypothorax . In contrast to the anterior bar, the posterior (back) end of the osteoderm is far more distinctive in its form, as it slopes and forms a bevel which is seen in Tecovasuchus , Kocurypelta and inconsistently among individuals of Paratypothorax andressorum. The underside of the osteoderm is generally smooth but preserves a pronounced ventral strut or keel that runs along the width of the bone. [1]
When viewed from above each paramedian osteoderm is rectangular in shape with a straight edge where the lateral osteoderms connect. A similar straight or sigmoid lateral edge is only present in two other typothoracines, Tecovasuchus and Kocurypelta. Observing the osteoderms from the front or back meanwhile shows that they are arched and made up of two main regions that connect at an oblique angle where the dorsal eminence, a raised region that forms the center of ossification, is located. [1]
The dorsal eminence forms the highest point of the osteoderms and is connected to a rounded ridge that spans the entire width of each osteoderm similar to Kocurypelta, running parallel to the posterior edge of the osteoderm. The eminence, which is surrounded by a distinct pattern of medium to large-sized pits and ridges that are collectively referred to as ornamentation, is also distinct in its location relative to the edges of the osteoderm. For example, similar to Desmatosuchus spurensis and Lucasuchus among others, the eminence is not in contact with the back edge of the osteoderm and it is further noted for being offset much further towards the midline than it is in other aetosaurs. Another prominent ridge is located in the posteromedial corner of the osteoderm. [1]
As typical for members of the clade Typothoracinae, the paramedian osteoderms are extremely wide, more than four times wider than they are long. Since the dorsal eminence is offset towards the midline, thus also shifting the flexion of the paramedian osteoderm, the medial portion of the paramedian osteoderm is much shorter than the lateral section, making up only about 40% of the total width. In addition to being of phylogenetic value, the great width of the osteoderms recovered from Venkatasuchus indicate that they were trunk osteoderms rather than neck osteoderms, with Haldar, Ray and Bandyopadhyay interpreting as having formed the early to middle trunk armour. Taking this placement into account and applying proportions similar to those of other typothoracines would suggest that the complete armour would have been disc-like in its appearance. [1]
Overall the lateral osteoderms, which are located to the side of the main paramedian row, are described as reduced and horn-like, their convex anterior margin making them appear to curve backwards. They can generally be divided into a dorsal (upper) and ventral (lower) flange, which are highly asymmetric with a much larger ventral flange like in Paratypothorax, Rioarribasuchus and Tecovasuchus. The dorsal flange is short and triangular while the ventral flange is long and more rectangular. The connection point between the two is strongly flexed, meaning they meet at an acute angle, tho the specific degree of flexion varies within the row. At least two groups of lateral osteoderms are identified, Group I in which the ratio between width and length is less than 1:1 and the flanges meet at an angle between 40 and 50°, and Group II in which the ratio between width and length is greater than 1:1 and the angle sits between 25 and 30°. Group I encompasses the first four preserved lateral osteoderms, while the remaining fall into Group II. [1]
Multiple features of the osteoderms of Venkatasuchus indicate that it was a member of the Aetosaurinae, one of the major clades within Aetosauria and sister to Stagonolepidoidea. More specifically, Venkatasuchus falls within the Typothoracinae and is deeply nested in Paratypothoracini. Traits responsible for these results include the extreme width to length ratio, the narrow weakly raised anterior bar, medial offset of the dorsal eminence and the asymmetrical lateral osteoderms. Phylogenetic analysis indicates that the closest relative of Venkatasuchus was Kocurypelta silvestris from the Late Triassic of Poland. [1]
Aetosauria |
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The age of the Lower Dharmaram Formation has been a matter of debate which is only added to by the description of Venkatasuchus. Previously, Bandyopadhyay and Ray proposed that the Lower Dharmaram Formation was mid to late Norian in age based on the presence of a Nicrosaurus -like phytosaur and its correlation with the Löwenstein Formation in Germany, whereas other researchers suggests that the fauna postdates the Ischigualasto Formation, indicating its age to be late Norian to Rhaetian. The discovery of Venkatasuchus, a paratypothoracine, again pushes the potential age of the formation back in time, ranging from the early to middle Norian to Rhaetian, with the presence of a desmatosuchine aetosaur suggesting a middle Norian age at the least based on the stratigraphy of the Chinle Formation and Dockum Group. [1]
Venkatasuchus also has major implications for the geography of aetosaurs. Generally, aetosaurs are best represented from Laurasian formations in Europe and North America, whereas their Gondwanan record is comparably poor with the exception of South America as the westernmost region. This makes Venkatasuchus one of the few known aetosaurs from eastern and central Gondwana. One hypothesis goes that aetosaur diversification was highly dependent on the Carnial Pluvial Event, much like the spread of metoposaurids and phytosaurs. Typothoracines most likely appeared a little later, during the early Norian, while diversifying during the middle Norian to Rhaetian. Geographically, aetosaurs can be found in three major clusters. High latitudes in the south featuring early diverging forms, high latitudes in the north featuring late diverging forms and the taxa clustering in low latitudes of North America, Morocco and India which feature a mix of early and late diverging taxa. These clusterings of aetosaur diversity overlap with those of metoposaurids and phytosaurs with the exception of the more southern latitudes, though collection bias could be a factor at play. [1]
India in particular is known to display a mix of Laurasian and Gondwanan fauna during the Late Triassic, with both Venkatasuchus and the undescribed phytosaur having Laurasian affinities, while the dinosaurs of the region are more closely allied with Gondwanan groups. This may have been highly influenced by the position of India at the time, with the slow breakup of the supercontinent Pangea opening land bridges and removing environmental barriers to allow for the migration of animal groups into the region which was not possible in other parts of the world. [1]
The Lower Dharmaram Formation represents an archosaur dominated environment and in addition to Venkatasuchus was the home to a wide variety of animals. This includes dinosaurs such as the sauropodomorph Jaklapallisaurus and an undescribed neotheropod as well as a wide range of pseudosuchians including an undescribed phytosaur which may have been similar to Nicrosaurus . Another undescribed pseudosuchian from the formation is a second type of aetosaur that more closely resembles the only distantly related Desmatosuchus. While archosaurs were plentiful, including groups of biostratigraphic importance like phytosaurs and aetosaurs, animals like metoposaurid temnospondyls and rhynchosaurs are as of yet unknown from the region. [1]
Aetosaurs are heavily armored reptiles belonging to the extinct order Aetosauria. They were medium- to large-sized omnivorous or herbivorous pseudosuchians, part of the branch of archosaurs more closely related to crocodilians than to birds and other dinosaurs. All known aetosaurs are restricted to the Late Triassic, and in some strata from this time they are among the most abundant fossil vertebrates. They have small heads, upturned snouts, erect limbs, and a body ornamented with four rows of plate-like osteoderms. Aetosaur fossil remains are known from Europe, North and South America, parts of Africa, and India. Since their armoured plates are often preserved and are abundant in certain localities, aetosaurs serve as important Late Triassic tetrapod index fossils. Many aetosaurs had wide geographic ranges, but their stratigraphic ranges were relatively short. Therefore, the presence of particular aetosaurs can accurately date a site in which they are found.
Calyptosuchus is an extinct genus of aetosaur from the Late Triassic of North America. Like other aetosaurs, it was heavily armored and had a pig-like snout used to uproot plants.
Acaenasuchus is an extinct genus of pseudosuchian, endemic to what would be presently be known as Arizona during the Late Triassic, specifically during the Carnian and Norian stages of the Triassic. Acaenasuchus had a stratigraphic range of approximately 11.5 million years. Acaenasuchus is further categorized as one of the type fauna that belong to the Adamanian LVF, based on the fauna of the Blue Mesa Member of the Chinle Petrified Forest Formation of Arizona, where Acaenasuchus was initially discovered.
Typothorax is an extinct genus of typothoracine aetosaur that lived in the Late Triassic. Its remains have been found in North America. Two species are known: T. coccinarum, the type species, and T. antiquum.
Lucasuchus is an extinct genus of aetosaur. Fossils have been found from the Bull Canyon Formation of the Dockum Group outcropping in the Revuelto Creek locality in Quay County, New Mexico. All specimens date back to the Norian stage of the Late Triassic. The genus was named in 1995 after the American paleontologist Spencer G. Lucas.
Paratypothorax is an extinct genus of aetosaur, known from a single species, Paratypothorax andressorum. It was a broadly distributed member of the group found in Germany, North America, and possibly parts of Gondwana. The best specimens come from Germany, though for more than a century they were mistakenly considered phytosaur armor. Paratypothorax was a large and wide-bodied typothoracine aetosaur, as well as the namesake of the tribe Paratypothoracisini.
Tecovasuchus is an extinct genus of aetosaur. It is known primarily from osteoderms found from the Tecovas Formation in Texas, which is Late Triassic in age, dating back to the lower Norian. Material is also known from several other localities of the Chinle Group in New Mexico and Arizona, such as older Carnian outcrops and younger Rhaetian outcrops. Specimens of Tecovasuchus have been collected from the Tecovas Formation, the Bluewater Creek Formation, and the Los Esteros Member of the Santa Rosa Formation.
Typothoracinae is a clade of aetosaurs within the subfamily Aetosaurinae. It was originally defined as a stem-based taxon including all aetosaurs closer to Typothorax than to Stagonolepis or Desmatosuchus. This definition was later expanded to specifically exclude Aetosaurus; as of 2016, Typothoracinae is defined as the least inclusive clade containing Typothorax and Paratypothorax, but not Aetosaurus,Stagonolepis, or Desmatosuchus. The clade was first named in 2007 under the spelling Typothoracisinae, after its namesake Typothorax. However, this spelling was based on incorrect taxonomic nomenclature, and the clade's name was corrected to Typothoracinae in 2016.
Aetosaurinae is one of the two main clades of aetosaurs, the other being Desmatosuchia. It is a stem-based taxon defined as all aetosaurs more closely related to Aetosaurus than Desmatosuchus. Aetosaurinae currently comprises Aetosaurus, similar forms such as Coahomasuchus and Stenomyti, and the widespread and successful aetosaur clade Typothoracinae.
Paratypothoracini is a clade of aetosaurs within the group Typothoracinae. It is a node-based taxon that includes Rioarribasuchus (=Heliocanthus), Paratypothorax, Tecovasuchus, and all descendants of their most recent common ancestor. The clade was first named in 2007 under the spelling Paraypothoracisini, after its namesake Paratypothorax. However, this spelling was based on incorrect taxonomic nomenclature, and the clade's name was corrected to Paratypothoracinae in 2016.
Desmatosuchinae is a major subfamily of aetosaurs within the clade Desmatosuchia. It is a stem-based taxon defined as all aetosaurs more closely related to Desmatosuchus than to Stagonolepis,Aetosaurus, or Paratypothorax.
Redondasuchus is an extinct genus of aetosaur. It may be a junior synonym of Typothorax coccinarum, another aetosaur. Redondasuchus is a member of the clade Typothoracisinae within the subfamily Aetosaurinae, and lived during the middle Norian stage of the Late Triassic. Material belonging to the genus has been found from the Redonda Formation in east-central New Mexico. The type species, R. reseri, was named in 1991 after having been referred to as a species of Typothorax since 1985. A second species, R. rineharti, was described in 2006.
Sierritasuchus is an extinct genus of aetosaur in the subfamily Desmatosuchinae. It is known from a small holotype skeleton from the Late Triassic Tecovas Formation of Texas. This skeleton was discovered in 1939 and was originally assigned to the genus Desmatosuchus. It was placed in its own genus in 2008 after having been in the collections of the University of Michigan Museum of Paleontology, with the type species being S. macalpini. The generic name refers to Sierrita de la Cruz Creek where the holotype was found, and the specific name refers to Archie MacAlpin, who discovered the skeleton. Based on the histology of the scutes of the holotype, the individual was a subadult that was not fully grown.
Tarjadia is an extinct genus of erpetosuchid pseudosuchian, distantly related to modern crocodilians. It is known from a single species, T. ruthae, first described in 1998 from the Middle Triassic Chañares Formation in Argentina. Partial remains have been found from deposits that are Anisian-Ladinian in age. Long known mostly from osteoderms, vertebrae, and fragments of the skull, specimens described in 2017 provided much more anatomical details and showed that it was a fairly large predator. Tarjadia predates known species of aetosaurs and phytosaurs, two Late Triassic groups of crurotarsans with heavy plating, making it one of the first heavily armored archosaurs. Prior to 2017, most studies placed it outside Archosauria as a member of Doswelliidae, a family of heavily armored and crocodile-like archosauriforms. The 2017 specimens instead show that it belonged to the Erpetosuchidae.
Polesinesuchus is an extinct genus of stagonolepidid aetosaur known from the Late Triassic of southern Brazil. Fossils have been found from the Santa Maria Supersequence of the late Carnian and early Norian stages, making Polesinesuchus one of the oldest aetosaurs. It contains a single species, Polesinesuchus aurelioi, the fifth aetosaur species known from South America to date. Anatomical evidence suggests that Polesinesuchus likely represents a juvenile individual of the contemporary Aetosauroides.
Gorgetosuchus is an extinct genus of aetosaur from the Late Triassic of the North Carolina, represented by the type species Gorgetosuchus pekinensis. It is mainly known from osteoderms, including the front half of an articulated carapace. Gorgotesuchus is typically considered a basal desmatosuchin, though alternative interpretations exist.
Scutarx is an extinct genus of Aetosauriformes, most commonly regarded by its species name Scutarx deltatylus. Scutarx lived around 230 million years ago during the Carnian and Norian stage of the Late Triassic. Scutarx are “medium sized” paramedian osteoderms belonging to the clade Aetosauria, a heavily armored and more herbivorous cousin of crocodiles.
Apachesuchus is an extinct genus of aetosaur from the Late Triassic of New Mexico. It is only known from several paramedian osteoderms discovered in Quay County in eastern New Mexico. This area belongs to the late Norian-age Quay Member of the Redonda Formation. Unique among aetosaurs, its osteoderms are nearly completely smooth, without strong pits or grooves. The left dorsal paramedian has a relatively high width-to-length ration, suggesting that Apachesuchus is a wide-bodied aetosaur within the clade Typothoracinae.
Kryphioparma is an extinct genus of aetosaur from the Late Triassic Blue Mesa Member of the Chinle Formation, Arizona. It is the oldest known member of the subfamily Typothoracinae, and is currently only known from five isolated and incomplete dorsal osteoderms. Regardless, said osteoderms show a clear mix of features that do not match any other known aetosaur and were thus used as the basis for a new genus and species in 2023. The genus is monotypic, only including a single species, Kryphioparma caerula.
Garzapelta is an extinct genus of aetosaur from the Late Triassic Cooper Canyon Formation containing a single species, G. muelleri. Garzapelta is known primarily from an associated collection of osteoderms, although some other bones such as ribs are also known. The anatomy of Garzapelta's armour displays a mix of features otherwise seen in Rioarribasuchus chamaensis, a member of the Paratypothoracini, and taxa of the subfamily Desmatosuchinae. This mix of characters is so distinct that phylogenetic analysis yielded different results based on what parts of the osteoderms were used, suggesting that the current dataset does not account for convergent evolution in osteoderm anatomy. Reyes, Martz and Small suggest that Garzapelta was likely a paratypothoracin that simply evolved lateral osteoderms similar to those of desmatosuchins, reasoning that its armour does not articulate in the way seen in members of the latter group.