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The neotype skull of the Indian phytosaur Parasuchus hislopi Lydekker, 1885 (ISI R42) is re-evaluated and compared with the type material of other basal phytosaurs. Parasuchus hislopi is extremely similar to species previously placed in Paleorhinus (P. bransoni and P. angustifrons), sharing with them such characters as a series of nodes on the lateral surface of the jugal, paired ridges on the squamosal and a frontal depression. Parasuchus hislopi represents a valid species: it can be distinguished from P. bransoni by a relatively low narial eminence and P. angustifrons by the absence of paired nasal depressions. Inclusion of Parasuchus hislopi in a phylogenetic analysis of phytosaurs recovers it in a well-supported clade with P. bransoni and P. angustifrons. Parasuchus is considered the senior synonym of Paleorhinus and Arganarhinus. Parasuchus (here considered to include P. hislopi, P. angustifrons, P. bransoni and P. magnoculus) has a broad circum-Pangaean distribution, with species occurring in the south-western United States, Morocco, central Europe and India. Phytosaur higher-level taxonomy is also revised: Parasuchidae is redefined to include ‘Paleorhinus-grade’ phytosaurs and the later-diverging Mystriosuchinae (the group formerly known as Phytosauridae), and Pseudopalatinae is renamed Mystriosuchini for reason of priority.

Phytosaurs are a clade of large, carnivorous pseudosuchian archosaurs from the Late Triassic with a near cosmopolitan distribution. Their superficial resemblance to longirostrine (long-snouted) crocodylians, such as gharials, has often been used in the past to infer ecological and behavioural convergence between the two groups. Although more than thirty species of phytosaur are currently recognised, little is known about the endocranial anatomy of this clade. Here, we describe the endocranial anatomy (including the brain, inner ear, neurovascular structures and sinus systems) of the two non-mystriosuchine phytosaursParasuchus angustifrons(=“Paleorhinus angustifrons”) andEbrachosuchus neukamifrom the Late Triassic of Germany based on digital reconstructions. Results show that the endocasts of both taxa are very similar to each other in their rostrocaudally elongate morphology, with long olfactory tracts, weakly demarcated cerebral regions and dorsoventrally short endosseous labyrinths. In addition, several sinuses, including large antorbital sinuses and prominent dural venous sinuses, were reconstructed. Comparisons with the endocranial anatomy of derived phytosaurs indicate that Phytosauria is united by the presence of elongate olfactory tracts and longitudinally arranged brain architecture—characters which are also shared with Crocodyliformes. However, a substantial morphological variability is observed in the cephalic and pontine flexure and the presence of a pineal organ across the different phytosaur species. These results suggest that the endocranial anatomy in Phytosauria generally follows a plesiomorphic pattern, with moderate variation within the clade likely resulting from divergent sensory and behavioural adaptations.

Two almost complete skeletons of a new eosuchian reptile, Malerisaurus robinsonae n.sp., were discovered as the presumable gastric contents of ‘twin’ skeletons of Parasuchus hislopi . The specimens are from fluvial flood plain deposits of the late Triassic Maleri Formation of the Gondwana supergroup, India. The osteology of Malerisaurus is described in detail. Malerisaurus was a small, gracile, long-necked eosuchian, facultatively bipedal, and probably able to climb trees or to take to the water when alarmed. It is comparable to modern bipedal lizards in size, proportions and inferred activities. The skull, although showing some carnivorous adaptation, is relatively unspecialized and indicates an insectivorous diet. Because Malerisaurus shows such a combination of primitive and advanced features as a diapsid skull, unossified laterosphenoid, lack of antorbital and mandibular fenestrae, slender limbs, primitive girdles, distinctive elongated cervicals and lack of dermal armour, it is assigned to the suborder Prolacertiformes of the order Eosuchia. A classification of Prolacertiformes indicates four families within this suborder: Petrolacosauridae, Protorosauridae, Prolacertidae and Tanystropheidae. Malerisaurus is tentatively allied to Protorosaurus in the family Protorosauridae; in neither genus is the temporal region of the skull adequately known. Malerisaurus furnishes detailed information about the skeletal morphology of what may be a hitherto undocumented lineage of eosuchian reptiles.