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Temporal range: Lopingian (Wuchiapingian to Changhsingian), 259–251.9 Ma[1][2]
Mount of one of the first two described skeletons of I. alexandri (PIN 1758), exposed at the Museo delle Scienze, Trento, Italy
Scientific classification Edit this classification
Domain: Eukaryota
Kingdom: Animalia
Phylum: Chordata
Clade: Synapsida
Clade: Therapsida
Clade: †Gorgonopsia
Family: †Gorgonopsidae
Subfamily: †Inostranceviinae
Genus: †Inostrancevia
Amalitsky, 1922
Type species
†Inostrancevia alexandri
Amalitsky, 1922
Other species
Synonyms
List of synonyms
  • Synonyms of genus
      • Inostranzevia Amalitsky, 1922
      • Amalitzkia Pravoslavlev, 1927
    Synonyms of I. alexandri
      • I. proclivis Pravoslavlev, 1927
    Synonyms of I. latifrons
      • Amalitzkia vladimiri Pravoslavlev, 1927
      • Amalitzkia annae Pravoslavlev, 1927
      • I. vladimiri Vyushkov, 1953

Inostrancevia is an extinct genus of large carnivorous therapsids which lived during the Late Permian in what is now European Russia and Southern Africa. The first-known fossils of this gorgonopsian were discovered in the context of a long series of excavations carried out from 1899 to 1914 in the Northern Dvina, Russia. Among these are two near-complete skeletons embodying the first described specimens of this genus. It is also the first gorgonopsian identified in Russia. Several other fossil materials were discovered there, and the various finds led to confusion as to the exact number of valid species, before only two of them were formally recognized, namely I. alexandri and I . latifrons. A third species, I. uralensis, was erected in 1974, but the fossil remains of this taxon are very thin and could come from another genus. More recent research carried out in South Africa aand Tanzania has discovered specimens identified as belonging to this genus, with the South African specimens being classified within the species I. africana. The whole genus is named in honor of Alexander Inostrantsev, professor of Vladimir P. Amalitsky, the paleontologist who described the taxon.

Possessing a skull measuring approximately 40 to 60 cm (16 to 24 in) long depending on the species, all for a body length reaching 3 to 3.5 m (9.8 to 11.5 ft), Inostrancevia is the largest known gorgonopsian, being rivaled in size only by the imposing Rubidgea. It has a broad and elongated skull equipped with large oval-shaped temporal fenestrae. It also has very advanced dentition, possessing large canines, the longest of which can reach 15 cm (5.9 in) and which may have been used to shear the skin of prey. Like most other gorgonopsians, Inostrancevia had a particularly large jaw opening angle, which would have allowed it to inflict fatal bites. Gorgonopsians in general would have been relatively fast predators, killing their prey by delivering slashing bites with their saber teeth. The skeleton is robustly constructed, but new studies are necessary for a better anatomical description and understanding about its paleobiological functioning.

Gorgonopsians were a group of carnivorous stem mammals with saber teeth that disappeared at the end of the Permian. The first classifications placed Inostrancevia as close to African taxa before 1948, the year in which Friedrich von Huene erected a distinct family, Inostranceviidae. Although this model was mainly followed in the scientific literature of the 20th and early 21st centuries, phylogenetic analysis published since 2018 consider it to belong to a group of derived Russian origin gorgonopsians, now classified alongside the genera Suchogorgon, Sauroctonus and Pravoslavlevia, the latter and Inostrancevia forming the subfamily Inostranceviinae. According to the Russian and African fossil records, the faunas where Inostrancevia is recorded were river ecosystems containing many tetrapods, where it appears to have been the main predator. These faunas were mainly occupied by dicynodonts and pareiasaurs, which would most likely have constituted its prey. In the Russian territory, Inostrancevia would have been the only large gorgonopsian present, while it would have been briefly contemporary with the rubidgeines in Tanzania. When the rubidgeines disappeared from South African territory, Inostrancevia would have in turn occupied the role of apex predator before disappearing in turn during the Permian-Triassic extinction.

Research history

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Initial finds and naming

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During the 1890s, Russian paleontologist Vladimir Amalitsky discovered freshwater sediments dating from the Upper Permian in Northern Dvina, Arkhangelsk Oblast, northern European Russia. The locality, known as PIN 2005, consists of a creek with sandstone and lens-shaped exposures in a bank escarpment, containing many particularly well-preserved fossil skeletons.[3] This type of fauna from this period, previously known only from South Africa and India, is considered as one of the greatest paleontological discoveries of the late 19th and early 20th centuries.[4] After the preliminary reconnaissance of the place, Amalitsky conducts systematic research with his companion Anna P. Amalitsky [ru].[3] The first excavations began in 1899,[3][4][5] and several of her findings where sent to Warsaw, Poland, in order to be prepared there.[6] The exhumations of the fossils then lasted until 1914,[3] when the research stopped due to the start of the World War I.[7] When this event begins, Amalitsky tries to save his collection of fossils residing in Warsaw in order to transfer it to the Nizhny Novgorod oblast. However, the arrival of the October Revolution in 1917 and the changing politics within the country indirectly led to his death in December of the same year. Subsequently, his fossil collection was transferred to Leningrad and became an integral part of the geological department of the city's university. During World War II, part of the fossils from the collection were transferred to the Paleontological Institute of the Russian Academy of Sciences in Moscow.[8]

 
Lectotype skeleton of I. alexandri (PIN 2005/1578)

Among all the fossils Amalitsky described before his death are two remarkably complete skeletons of large gorgonopsians, now cataloged as PIN 1758 and PIN 2005/1578. After identification, he assigned the two specimens within a new genus and species, which he named Inostranzevia alexandri,[3] the specimen PIN 2005/1578 being later recognized as its lectotype.[9][10][11] These two specimens constitute the first known quasi-complete postcranial remains identified among gorgonopsians[12] as well as the first representative of this group to have been identified in Russia.[5][13] Although the taxon was not officially described posthumously until 1922,[3] the use of this name in scientific literature dates back to the beginning of the 20th century, notably in the works of Friedrich von Huene and Edwin Ray Lankester.[14][15][16][17] Taxonomic issues regarding the original naming of the genus are the subject of a study which should be published later.[17] Although the etymology of the genus and type species is not provided in the earliest-known descriptions of the taxon, the full name of the animal is named in honor of the renowned geologist Alexander Inostrantsev [ru],[10] who was one of Amalitsky's teachers.[8] Amalitsky's article generally describes all the fossil discoveries made in the Northern Dvina, and not Inostrancevia itself, the article mentioning that further research on this gorgonopsian is subject to research.[3]

20th century further research

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In 1927, one of Amalitsky's colleagues, Pavel Pravoslavlev, wrote two works, including a book, which are the first in-depth descriptions of the fossils today attributed to this taxon.[18][19] In his works, Pravoslavlev changed the typography of the name "Inostranzevia" to "Inostrancevia".[a] Although the original name has been used a few times in recent scientific literature,[21] the second term has since entered into universal usage and must be maintained according to the rule of article 33.3.1 of the ICZN.[13] Among the many species of Inostrancevia erected and described on its part,[22] only I. latifrons is found to be valid. The holotype of this species, cataloged PIN 2005/1857, consists of a large skull missing the lower jaw, discovered in the same locality as that of the first known specimens of I. alexandri. Another skull was also discovered in the same locality as the holotype, while an incomplete skeleton was discovered in the village of Zavrazhye, located in Vladimir Oblast.[23][9][10] The specific name latifrons comes from the Latin latus "broad" and frōns "forehead", in reference to the size and the more robust cranial constitution than that of I. alexandri.[24]

In 1974, Leonid Petrovich Tatarinov carried out a large revision of the theriodonts then known in the USSR. In his work, he revises the validity of the taxa erected by Pravoslavlev and describes a third species of Inostrancevia, I. uralensis, on the basis of part of the skull. The holotype specimen, cataloged as PIN 2896/1, consists of a left basioccipital having been discovered in the locality of Blumental-3, located in the Orenburg Oblast. The specific name uralensis refers to the Ural River, where the holotype specimen of the taxon was found.[10][13][25] However, due to its poor fossil preservation of this species, Tatarinov argues that it is possible that I. uralensis could belong to a new genus of large gorgonopsians.[26]

21st century research

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In 2010, the Bloemfontein Museum sent an expedition to the farm of Nooitgedacht 68, located near the town of Bethulie, in the Karoo Basin, South Africa. It was during this same expedition that Nthaopa Ntheri discovered a partial skeleton of a large gorgonopsian which include an almost complete skull, cataloged as NMQR 4000. During a second expedition launched the following year, John Nyaphuli discovers another partial skeleton similar to that of the previously discovered specimen, cataloged as NMQR 3707.[2] The existence of these two specimens are mentioned in 2014 in the chapter of a work listing the discoveries made at this farm,[27] but it was not until 2023 that Christian F. Kammerer and his colleagues made the first official description concerning these latter. Their descriptions unexpectedly confirm that these specimens belong to Inostrancevia, which is a significant first given that the genus was historically only reported in Russia. The specimens nevertheless possessed some differences allowing them to be distinguished from the Russian lineages, they were then classified in the newly erected species I. africana, the specimen NMQR 4000 being designated as the holotype of this species, while NMQR 3707 was bequeathed as a paratype. The specific name, meaning "Africa" ​​in Latin, refers to the first proven presence of its kind within that continent. However, the article officially describing this animal focuses primarily on the stratigraphic significance of the findings and is only a brief introduction to the anatomy of the new fossil material, being the subject for future study.[2]

Earlier, in June 2007, a team of paleontologists discovered an isolated left premaxilla, cataloged as NMT RB380, in the Ruhuhu Basin, southern Tanzania. The fossil bone was subsequently scanned and identified as Inostrancevia sp. in a 2024 study led by Anna J. Brant and Christian A. Sidor.[28]

Synonyms and formerly assigned species

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In his two works published in 1927, Pravoslavlev also named several additional gorgonopsian taxa,[18][29][b]. In their broad revision of the classification of therapsids published in 1956, David Watson and Alfred Romer recognized without argumentation almost all of the taxa erected by Pravoslavlev as valid,[30] but their opinions were never followed in subsequent works.[31][9][2] In addition of I. latifrons, Pravoslavlev names and describes two additional species of the genus Inostrancevia: I. parva and I. proclivis.[32] In 1940, the paleontologist Ivan Yefremov expressed doubts about this classification, and considered that the holotype specimen of I. parva should be viewed as a juvenile of the genus and not as a distinct species.[13][33] It was in 1953 that Boris Pavlovich Vyuschkov completely revised the species named for Inostrancevia. For I. parva, he moves it to a new genus, which he names Pravoslavlevia, in honor of the original author who named the species.[34] Although being a distinct and valid genus, Pravoslavlevia turns out to be a closely related taxon.[9][13][2] Also in his article, he considers that I. proclivis is a junior synonym of I. alexandri, but remains open to the question of the existence of this species, arguing his opinion with the insufficient preservation of type specimens.[34] This taxon will be definitively judged as being conspecific to I. alexandri in the revision of the genus carried out by Tatarinov in 1974.[35]

In the first work published earlier the same year, Pravoslavlev erected another genus of gorgonopsians, Amalitzkia, with the type species A. annae.[18] In his larger work published subsequently, he erected a second species under the name of A. wladimiri.[36] The genus as well as the two species are named in honor of the couple of paleontologists who carried out the work on the first known specimens of I. alexandri.[18][36] In 1953, Vjuschkov discovered that the genus Amalitzkia is a junior synonym of Inostrancevia, renaming A. wladimiri to I. wladimiri,[34] before the latter was itself recognized as a junior synonym of I. latifrons by later publications.[9][23] For some unclear reason, Vjuschkov refers A. annae as a nomen nudum,[34] when his description is quite viable.[18] Just like A. wladimiri, A. annae will be synonymized with I. latifrons by Tatarinov in 1974.[23]

In 2003, Mikhail F. Ivakhnenko erected a new genus of Russian gorgonopsian under the name of Leogorgon klimovensis, on the basis of a partial braincase and a large referred canine, both discovered in the Klimovo-1 locality, in the Vologda Oblast. In his official description, Ivakhnenko classifies this taxon among the subfamily Rubidgeinae, whose fossils are exclusively known from what is now Africa. This would therefore make Leogorgon the first known representative of this group to have lived outside this continent.[37] In 2008, however, Ivakhnenko noted that, due to its poorly known anatomy, Leogorgon could be a relative of the Russian Phthinosuchidae rather than the sole Russian representative of the Rubidgeinae.[38] In 2016, Kammerer formally rejected Ivakhnenko's classifications, because the holotype braincase of Leogorgon likely came from a dicynodont, while the attributed canine tooth is indistinguishable from that of Inostrancevia. Since then, Leogorgon has been recognized as a nomen dubium of which part of the fossils possibly come from Inostrancevia.[39]

Other species belonging to distinct lineages were sometimes inadvertently classified in the genus Inostrancevia. For example, in 1940, Efremov classifies a gorgonopsian of then-problematic status as I. progressus. However, in 1955, Alexey Bystrow moved this species to the separate genus Sauroctonus.[40][41][13][42] A large maxilla discovered in Vladimir Oblast in the 1950s was also assigned to Inostrancevia, but the fossil would be reassigned to a large therocephalian in 1997,[43] and later designated as the holotype of the genus Megawhaitsia in 2008.[44]

Description

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Scale chart, showing I. latifrons size compared to a human

Inostrancevia is a gorgonopsian with a fairly robust morphology, the Spanish paleoartist Mauricio Antón describing it as a "scaled-up version" of Lycaenops.[45] The numerous descriptions given to this taxon make it one of the most emblematic animals of the Permian period, mainly because of its large size among gorgonopsians, rivaled only by the South African genus Rubidgea,[13] the latter having a roughly similar size.[45] Gorgonopsians were skeletally robust, yet long-limbed for therapsids, with a somewhat dog-like stance, though with outwards-turned elbows.[46] It is unknown whether non-mammaliaform therapsids such as gorgonopsians were covered in hair or not.[47]

The specimens PIN 2005/1578 and PIN 1758, belonging to I. alexandri, are among the largest and most complete gorgonopsian fossils identified to date. Both specimens are around 3 m (9.8 ft) long,[45] with the skulls alone measuring over 50 cm (20 in).[3] However, I. latifrons, although known from more fragmentary fossils, is estimated to have a more imposing size, the skull being 60 cm (24 in) long, indicating that it would have measured 3.5 m (11 ft) and weighed 300 kg (660 lb).[48] The size of I. uralensis is unknown due to very incomplete fossils, but it appears to be smaller than I. latifrons.[49] The two known specimens of I. africana are among the largest gorgonopsians to have been discovered in Africa, the holotype skull measuring 44.2 cm (17.4 in), while that of the paratype reaches 48.1 cm (18.9 in). These proportions are matched only by the largest known specimens of Rubidgea.[2] Based on comparisons with various other gorgonopsians, the Tanzanian specimen of Inostrancevia would have had a skull with an estimated length of between 38.5 to 69 cm (15.2 to 27.2 in) long. However, the authors mention that it is difficult to know if the specimen would have been similar in size to those of recognized species.[28]

Skull

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Close-up of a skull referred to I. alexandri

The overall shape of the skull of Inostrancevia is similar to those of other gorgonopsians,[3] although it has many differences allowing it to be distinguished from African representatives.[13] It has a broad back skull, a raised and elongated snout, relatively small eye sockets and thin cranial arches.[49][38][45] The pineal foramen is located near the posterior edge of the parietals and rests on a strong projection in the middle of an elongated hollow like impression.[3] The sagittal suture is reinforced with complex curvatures. The ventral surface of the palatine bones is completely smooth, lacking traces of palatine teeth or tubercles. Just like Viatkogorgon, the top margin of the quadrate is thickened.[38] The three recognized Russian species have notable characteristics between them: I. alexandri is distinguished by its relatively narrow occiput, a broad and rounded oval temporal fenestra and the transverse flangues of the pterygoid with teeth; I. latifrons is distinguished by a comparatively lower and broader snout, larger parietal region, fewer teeth and a less developed palatal tuberosities; and I. uralensis is characterized by a transversely elongated oval slot-like temporal fenestra.[49]

 
Canine tooth of I. alexandri (top) and Leogorgon klimovensis (bottom)

The jaws of Inostrancevia are powerfully developed, equipped with teeth able to hold and tear the skin of prey. The teeth are also devoid of cusps and can be distinguished into three types: the incisors, the canines and the postcanines.[c] All teeth are more or less laterally compressed and have finely serrated front and rear edges. When the mouth is closed, the upper canines move into position at the sides of the mandible, reaching its lower edge.[3] The canines of Inostrancevia measuring between 12 cm (4.7 in) and 15 cm (5.9 in), they are among the largest identified among non-mammalian therapsids,[38] only the anomodont Tiarajudens have similarly sized canines.[51] In the upper and lower jaws, these canines are roughly equal in size and are slightly curved.[38] The incisors turn out to be very robust. The postcanine teeth are present on the upper jaw, on its slightly upturned alveolar edges. In contrast, they are completely absent from the lower jaw. There are indications that the tooth replacement would have taken place by the young teeth, growing at the root of the old ones and gradually supplanting them.[3] The capsule of the canines is very large, containing up to three capsules of replacement canines at different stages of development.[38]

Postcranial skeleton

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Although the postcranial anatomy of Inostrancevia was first described in detail in 1927 by Pravoslavlev,[52] new discoveries and anatomical descriptions of this taxon have led authors suggesting further revisions to broaden the skeletal understanding of the animal.[38][12][2] The skeleton of Inostrancevia is of very robust constitution,[3] mainly at the level of the limbs.[12] The ungual phalanges have an acute triangular shape.[3][38] Inostrancevia has the most autapomorphic postcranial skeleton identified on a gorgonopsian. The scapula of this latter is unmistakable, with an enlarged plate-like blade unlike that of any other known gorgonopsians, but its anatomy is also unusual, with ridges and thickened tibiae, especially at their joint margins.[12] The scapular blade of Inostrancevia being extremely enlarged,[13][53] its morphology will most likely be subject to future study regarding its paleobiological function.[12]

Classification

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Systematics

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From its original description published in 1922, Inostrancevia was immediately classified in the family Gorgonopsidae after anatomical comparisons made with the type genus Gorgonops.[3][20] This classification was maintained as such until 1948, when von Huene established a separate family of gorgonopsians, Inostranceviidae, to include Inostrancevia.[54] Huene's opinion was generally shared in various studies published subsequently during the 20th century and even into the 21st century, although with some alternative classifications.[55][56][57] In 1974, Tatarinov classified Pravoslavlevia as a sister taxon of Inostrancevia within this family.[56] In 1989, Denise Sigogneau-Russell proposes a similar classification, but moves the taxon reuniting the two genera as a subfamily, being renamed Inostranceviinae, and is classified in the more general family Gorgonopsidae.[53] In 2002, in his revision of the Russian gorgonopsians, Mikhail F. Ivakhnenko re-erects the family Inostranceviidae and classifies the taxon as one of the lineages of the superfamily "Rubidgeoidea", placed alongside the Rubidgeidae and Phtinosuchidae.[58] One year later, in 2003, he reclassifies Inostrancevia in the family Inostranceviidae, similar to Tatarinov's proposal, but the latter classifies it alone, making it a monotypic taxon.[37]

In a thesis written in 2007, German paleontologist Eva V. I. Gebauer carried out the very first phylogenetic analysis of gorgonopsians. Based on observations made on the occipital bones and canines, Gebauer moved Inostrancevia as a sister taxon to the Rubidgeinae, a lineage consisting of robust African gorgonopsians.[59] In 2016 Christian F. Kammerer regarded Gebauer's analysis as "unsatisfactory", citing that many of the characters used by her analysis were based upon skull proportions that are variable within taxa, both individually and ontogenetically (i.e. traits that change through growth).[39] In 2018, in their description of Nochnitsa and re-description of the skull of Viatkogorgon, Kammerer and Vladimir Masyutin propose that all Russian and African taxa should be separately grouped into two distinct clades. For Russian genera (except basal taxa), this relationship is supported by notable cranial traits, such as the close contact between pterygoid and vomer. The discovery of other Russian gorgonopsians and the relationship between them and Inostrancevia has never before been recognized for the simple reason that some authors undoubtedly compared them to African genera.[13] The classification proposed by Kammerer and Masyutin will serve as the basis for all other subsequent phylogenetic studies of gorgonopsians.[50][60] Using this model, the 2023 study by Kammerer and colleagues describing I. africana recovers it as a sister taxon to I. alexandri within the Russian origin clade.[2] As with previous classifications, Pravoslavlevia is still considered as the sister taxon of Inostrancevia.[13][50][60][2]

The following cladogram shows the position of Inostrancevia within the Gorgonopsia after Kammerer and Rubidge (2022):[60]

Gorgonopsia

Evolution

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Gorgonopsians form a major group of carnivorous therapsids whose oldest-known representatives come from South Africa and appear in the fossil record from the Middle Permian. During this period, the majority of representatives of this clade were quite small and their ecosystems were mainly dominated by dinocephalians, large therapsids characterized by strong bone robustness.[61] However, some genera, notably Phorcys, are relatively larger in size and already occupy the role of superpredator in the one of the oldest geological strata of the Karoo Supergroup.[60] Gorgonopsians were the first group of predatory animals to develop saber teeth, long before true mammals and dinosaurs evolved. This feature later evolved independently multiple times in different predatory mammal groups, such as felids and thylacosmilids.[62] Geographically, gorgonopsians are mainly distributed in the present territories of Africa and European Russia,[13] with, however, an indeterminate specimen having been identified in the Turpan Depression, in north-west China,[63] as well as a possible fragmentary specimen discovered in the Kundaram Formation, located in central India.[64] After the Capitanian extinction, gorgonopsians began to occupy ecological niches abandoned by dinocephalians and large therocephalians, and adopted an increasingly imposing size, which very quickly gave them the role of superpredators. In Africa, it is mainly the rubidgeines who occupy this role,[39] while in Russia, only Inostrancevia acquires as such,[13][50][65] the only known gorgonopsian and contemporary of this latter, Pravoslalevia, being considerably smaller.[66][9]

Paleobiology

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Hunting strategy

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Restoration of I. alexandri attacking Scutosaurus

One of the most recognizable characteristics of Inostrancevia (and other gorgonopsians, as well) is the presence of long, saber-like canines on the upper and lower jaws. How these animals would have used this dentition is debated. The bite force of saber-toothed predators (like Inostrancevia), using three-dimensional analysis, was determined by Stephan Lautenschlager and colleagues in 2020:[67] their findings detailed that, despite morphological convergence among saber-toothed predators, there is a range of methods of possible killing techniques. The similarly-sized Rubidgea is capable of producing a bite force of 715 newtons; although lacking the necessary jaw strength to crush bone, the analysis found that even the most massive gorgonopsians possessed a more powerful bite than other saber-toothed predators.[68] The study also indicated that the jaw of Inostrancevia was capable of a massive gape, perhaps enabling it to deliver a lethal bite, and in a fashion similar to the hypothesised killing technique of Smilodon (or 'saber-toothed cat').[67]

Antón provided an overview of gorgonopsian biology in is 2013 book, writing that despite their differences from saber-toothed mammals, many features of their skeletons indicated they were not sluggish reptiles but active predators. While their brains were relatively smaller than those of mammals, and their sideways placed eyes provided limited stereoscopic vision, they had well-developed turbinals in their nasal cavity, a feature associated with an advanced sense of smell, which would have helped them track prey and carrion. The canine saber teeth were used for delivering the slashing killing-bite, while the incisors, which formed an arch in front of the saber teeth, held the prey and cut the flesh while feeding. To allow them to increase their gape when biting, gorgonopsians had several bones in their mandibles that could move in relation to each other and had a double articulation with the skull—unlike in mammals where the rear joint articular bone has become the malleus ear bone.[69] Antón envisioned gorgonopsians would hunt by leaving their cover when prey was close enough, and use their relatively greater speed to pounce quickly on it, grab it with their forelimbs, and bite any part of the body that would fit in their jaws. Such a bite would cause a large loss of blood, but the predator would continue to try to bite vulnerable parts of the body.[70]

Motion

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Antón stated in 2013 that while the post-cranial skeletons of gorgonopsians were basically reptilian, their stance was far more upright than in more primitive synapsids, like pelycosaurs, which were more sprawling. Regular locomotion of gorgonopsians would have been similar to the "high walks" seen in crocodilians, wherein the belly is carried above the ground, with the feet pointing forwards, and the limbs carried under the trunk instead of to the sides. The forelimbs had a more horizontal posture than the hindlimbs, with the elbows pointing outwards during movement, but the gait of the hindlimbs would have resembled that of mammals. As in reptiles, the tail muscles (such as the caudofemoralis) were important in flexion of the hindlimb, whereas the tails of mammals are merely for balance. Their feet were probably plantigrade (where the soles were placed flat on the ground), though they were likely more swift and agile than their prey. Their feet were more symmetrical compared to the reptilian condition, making contact with the ground more efficient, similar to running mammals.[70]

Palaeoecology

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Paleoenvironment

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Restoration of I. latifrons chasing Scutosaurus

During the Late Permian when Inostrancevia lived, the Southern Urals (close in proximity to the Sokolki assemblage) were located around latitude 28–34°N and defined as a "cold desert" dominated by fluvial deposits.[71] The Salarevo Formation in particular (a horizon where Inostrancevia hails from) was deposited in a seasonal, semi-arid-to-arid area with multiple shallow water lakes which was periodically flooded.[72] The Paleoflora of much of European Russia at the time was dominated by a genus of peltaspermaceaen, Tatarina, and other related genera, followed by ginkgophytes and conifers. On the other hand, ferns were relatively rare and sphenophytes were only locally present.[71] There are also hygrophyte and halophyte plants in coastal areas as well as conifers that are more resistant to drought and higher altitudes.[73]

The fossil sites from which Inostrancevia was recorded contain abundant fossils of terrestrial and shallow freshwater organisms, including ostracods,[1] fishes, reptiliomorphs like Chroniosuchus and Kotlassia, the temnospondyl Dvinosaurus, the pareiasaur Scutosaurus, the dicynodont Vivaxosaurus and the cynodont Dvinia.[65][66][73][74] Inostrancevia was the top predator in its environment and could have preyed on the majority of the previously mentioned tetrapods.[15][65][66] Other smaller predators have existed alongside Inostrancevia, such as the smaller related gorgonopsian Pravoslavlevia and the therocephalian Annatherapsidus.[66][75]

According to the fossil record, the Upper Daptocephalus Assemblage Zone, from which I. africana is known, would have been a well-drained floodplain. The area preceding just before the Permian–Triassic extinction, this would explain why there is no more diversification of animals than in the older strata of the Balfour Formation.[2][76]

As in the other formations of the Karoo Basin, dicynodonts are the most common animals in the Upper Daptocephalus Assemblage Zone. Among the most abundant dicynodonts are Daptocephalus (hence the name of the site), Diictodon and Lystrosaurus. Few genera of therocephalians are known within the site, only Moschorhinus and Theriognathus having been listed. The presence of the cynodont Procynosuchus is also reported.[77] The gorgonopsians Arctognathus and Cyonosaurus should be present based on their wide temporal distribution within the Karoo Basin, but formal fossils have not yet been discovered. As in the Russian fossil record, I. africana would have been the main predator in the area, most likely preying on contemporary dicynodonts.[2]

Contemporary fauna

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Extinction

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Gorgonopsians, including Inostrancevia, disappeared in the Late Lopingian during the Permian–Triassic extinction event, mainly due to volcanic activities that originated in the Siberian Traps. The resulting eruption caused a significant climatic disruption unfavorable to their survival, leading to their extinction. Their ecological niches gave way to modern terrestrial ecosystems including sauropsids, mostly archosaurs, and among the few therapsids surviving the event, mammals.[78] However, some Russian gorgonopsians have already disappeared a little time before the event, having consequently abandoned some of their niches to large therocephalians.[44] Kammerer and his colleagues claimed that as the extinction of the rubidgeines in their respective territory of Africa, Inostrancevia migrated from Russia to take the role of apex predator within this place for a limited time. The presence of dicynodonts like Lystrosaurus would have been an opportunity for being a prey, as the latter thrived throughout the Permian–Triassic boundary.[2] However, an isolated left premaxilla of Inostrancevia from the Usili Formation in Tanzania during the earliest Lopingian age suggested otherwise, since the discovery of this specimen indicated that Inostrancevia already lived in Africa alongside other large rubidgeines such as Dinogorgon and Rubidgea before the latest Permian.[28]

See also

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Notes

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  1. ^ The latter name had already been changed previously by Samuel Wendell Williston in 1925,[20] but it was not until Pravoslavlev's publications that the taxon was mainly known under this designation.[13]
  2. ^ The existence of these taxa are already mentioned in the article describing I. alexandri[3] but were not officially named and described in detail until 1927.[29]
  3. ^ Previously identified as molars by Amalitsky,[3] this type of teeth was later redescribed as postcanine teeth, having a lack of functional range.[50]

References

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  4. ^ a b Benton et al. 2000, p. 4.
  5. ^ a b Gebauer 2007, p. 9.
  6. ^ Lankester 1905, p. 214–215.
  7. ^ Benton et al. 2000, p. 5.
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Bibliography

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