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Although there are problematic earliest Jurassic records, phytosaurs are thought to have become extinct during the Rhaetian. A newly-discovered left paramedian phytosaur osteoderm from a clay pit in Bonenburg, Kreis Höxter, North Rhine-Westphalia, Germany, is the youngest, well-dated phytosaur record. This osteoderm was found in a bone bed (Bone Bed 2) in the Contorta Beds of the Rhaetian Exter Formation. Palynology constrains the age of Bone Bed 2 to the late middle Rhaetian (ca. 203.5 million years ago). The Bonenburg osteoderm cannot be assigned to any named species. It most closely resembles some osteoderms from the Rhaetian of Halberstadt in Central Germany. Phytosaurs survived in Europe to at least the late middle Rhaetian, probably falling victim to the end-Triassic extinction event about two million years later.

Abstract Background The origins of all major living reptile clades, including the one leading to birds, lie in the Triassic. Following the largest mass extinction in Earth’s history at the end of the Permian, the earliest definite members of the three major living reptile clades, the turtles (Testudines), crocodylians and birds (Archosauria), and lizards, snakes, amphisbaenians, and Tuatara (Lepidosauria) appeared. Recent analyses of the Triassic reptile fossil record suggest that the earliest diversifications in all three of these clades were tightly controlled by abrupt paleoclimate fluctuations and concordant environmental changes. Yet, this has only been preliminarily tested using information from evolutionary trees. Phytosauria consists of superficially crocodylian-like archosaurs that either form the sister to the crown or are the earliest divergence on the crocodylian stem and are present throughout the Triassic, making this clade an excellent test case for examining this biogeographic hypothesis. Results Here, I describe a new phytosaur, Jupijkam paleofluvialis gen. et sp. nov., from the Late Triassic of Nova Scotia, Canada, which at that time sat in northern Pangaea near the northern terminus of the great central Pangean rift. As one of the northernmost occurrences of Phytosauria, J. paleofluvialis provides critical new biogeographic data that enables revised estimations of phytosaur historical biogeography along phylogenies of this clade built under multiple methodologies. Reconstructions of phytosaur historical biogeography based on different phylogenies and biogeographic models suggest that phytosaurs originated in northern Pangaea, spread southward, and then dispersed back northward at least once more during the Late Triassic. Conclusions The results presented in this study link phytosaur biogeography to major changes to Triassic global climate and aridity. Together with the earliest dinosaurs and several other reptile lineages, phytosaur diversification and migration appear to have been restricted by the formation and loss of arid belts across the Pangean supercontinent.

Although there are problematic earliest Jurassic records, phytosaurs are thought to have become extinct during the Rhaetian. A newly-discovered left paramedian phytosaur osteoderm from a clay pit in Bonenburg, Kreis Höxter, North Rhine-Westphalia, Germany, is the youngest, well-dated phytosaur record. This osteoderm was found in a bone bed (Bone Bed 2) in the Contorta Beds of the Rhaetian Exter Formation. Palynology constrains the age of Bone Bed 2 to the late middle Rhaetian (ca. 203.5 million years ago). The Bonenburg osteoderm cannot be assigned to any named species. It most closely resembles some osteoderms from the Rhaetian of Halberstadt in Central Germany. Phytosaurs survived in Europe to at least the late middle Rhaetian, probably falling victim to the end-Triassic extinction event about two million years later. [ABSTRACT FROM AUTHOR]

Numerous isolated teeth recovered from the Upper Triassic Tiki Formation of India have high, cylindrical, triangular to conical crowns with serrated mesial and distal carinae, and oval/subcircular and elliptical crown bases. Within this overall morphology, the teeth are subdivided into six morphotypes based on crown proportions, nature of carinae and serration and crown-base ratios. These ziphodont teeth are compared with those of other dominant Late Triassic carnivores of India to show similarity with that of the phytosaurs based on their shape, recurved nature, crown proportions, the presence of carina(e), nature of serrations and serration density. The different morphotypes reflect positional heterodonty, and three upper jaw dental sets are identified. This finding is corroborated by PCA, where the morphotypes form distinctly separate clusters, though partial overlapping of these convex hull polygons suggests that these teeth belonged to a single phytosaur taxon. As tripartite dentition is a derived condition; it may be concluded that these isolated teeth belonged to a more derived phytosaur, yet to be recovered from the Tiki Formation. The study highlights the importance of examining isolated teeth in order to identify the fossil forms which are yet to be discovered. [ABSTRACT FROM AUTHOR]

Spinosaurids are a highly morphologically specialized clade of large tetanuran theropod dinosaurs, characterized by their proportionally long, narrow snouts and conical teeth with fluted surfaces. The unusual morphology of spinosaurids has been usually compared with modern crocodilians, but distinct differences between them have been reported as well. Here, numerous craniodental characters that are shared by spinosaurids and large, robust phytosaurs often termed as "brachyrostral" forms are reviewed. Phytosaurs are a clade of carnivorous archosauriforms that resemble crocodilians in overall morphology, and as such a similar lifestyle has been inferred for them as well. Although based on preliminary observations, the shared craniodental characters of spinosaurids and "brachyrostral" phytosaurs, including those not shared with crocodilians, raise the possibility that at least some aspects of the lifestyle of these extinct archosauriform clades were more similar to each other rather than to that of crocodilians [ABSTRACT FROM AUTHOR]

Phytosaurs are a group of carnivorous, semi-aquatic archosaurian reptiles that attained an almost global distribution during the Late Triassic. We here describe a new species of the phytosaur genus Mystriosuchus from the Norian Dachstein Limestone of Austria, from a marine lagoonal depositional environment. The new Austrian material comprises remains of at least four individuals of similar size (c. 4 m in total length) found in association but disarticulated, and includes one complete and two partial skulls and postcrania. All of these specimens apparently represent a single taxon, which is distinguished by numerous anatomical features from the two previously named Mystriosuchus species. Maximum parsimony analysis of a comprehensive morphological dataset provides strong statistical support for the phylogenetic position of the new Austrian taxon in Mystriosuchus , as the sister taxon to a clade comprising M. planirostris and M. westphali. Histological analysis suggests that the Austrian phytosaur specimens represent individuals that were at least eight years old at time of death, but which had not yet reached skeletal maturity. Taphonomic and palaeoenvironmental data suggest that these phytosaurs were living in the marine lagoon in which they were preserved, providing the strongest evidence to date of marine adaptations in phytosaurs. [ABSTRACT FROM AUTHOR]

Detailed description and phylogenetic assessment of a phytosaur skull collected from the Tiki Formation of the Rewa Gondwana Basin of India and earlier diagnosed as Parasuchus hislopi, show that it pertains to a new genus and species, Volcanosuchus statisticae. The new taxon is characterized by marginal overlapping of the nostrils by the antorbital fenestrae, external nares situated on a bulbous and raised dome, the lateral surface of the jugal ornamented by a prominent ridge defined by multiple tubercles and radiating thread‐like structures, and distinct ornamentation patterns on the rostrum and skull table. Phylogenetic analysis nests Volcanosuchus within Mystriosuchinae, where it forms a sister taxon to (Rutiodon + Leptosuchomorpha) and marks the transition between the basal Parasuchidae and more derived Mystriosuchinae phytosaurs. Evolution of the phytosaur skulls resulted in changes from non‐overlapping nostril and antorbital fenestra to an overlapping state, anteroposterior elongation of the exoccipital–supraoccipital shelf, appearance of a median ridge on the basioccipital, and reduction of the supratemporal fenestra. Considerable faunal overlap of the Tiki Formation is evident with the lower Maleri Formation, which is late Carnian based on the occurrence of Hyperodapedon, Parasuchus and Exaeretodon. The Tiki Formation correlates with the Ischigualasto Formation of Argentina, the upper part of the Santa Maria Formation, and the overlying lower Caturrita Formation of Brazil, the Isalo II Beds of Madagascar, Lossiemouth Sandstone of Scotland, and the lower Tecovas Formation of the Chinle Group of North America, and ranges from late Carnian to early/middle Norian. [ABSTRACT FROM AUTHOR]

This corrects the article DOI: 10.1038/srep46028.

Following the end-Permian extinction, terrestrial vertebrate diversity recovered by the Middle Triassic, and that diversity was now dominated by reptiles. However, those reptilian clades, including archosaurs and their closest relatives, are not commonly found until ~30 million years post-extinction in Late Triassic deposits despite time-calibrated phylogenetic analyses predicting an Early Triassic divergence for those clades. One of these groups from the Late Triassic, Phytosauria, is well known from a near-Pangean distribution, and this easily recognized clade bears an elongated rostrum with posteriorly retracted nares and numerous postcranial synapomorphies that are unique compared with all other contemporary reptiles. Here, we recognize the exquisitely preserved, nearly complete skeleton of Diandongosuchus fuyuanensis from the Middle Triassic of China as the oldest and basalmost phytosaur. The Middle Triassic age and lack of the characteristically-elongated rostrum fill a critical morphological and temporal gap in phytosaur evolution, indicating that the characteristic elongated rostrum of phytosaurs appeared subsequent to cranial and postcranial modifications associated with enhanced prey capture, predating that general trend of morphological evolution observed within Crocodyliformes. Additionally, Diandongosuchus supports that the clade was present across Pangea, suggesting early ecosystem exploration for Archosauriformes through nearshore environments and leading to ease of dispersal across the Tethys.

Phytosaurs are a group of large, semi‐aquatic archosaurian reptiles from the Middle–Late Triassic. They have often been interpreted as carnivorous or piscivorous due to their large size, morphological similarity to extant crocodilians and preservation in fluvial, lacustrine and coastal deposits. However, these dietary hypotheses are difficult to test, meaning that phytosaur ecologies and their roles in Triassic food webs remain incompletely constrained. Here, we apply dental microwear textural analysis to the three‐dimensional sub‐micrometre scale tooth surface textures that form during food consumption to provide the first quantitative dietary constraints for five species of phytosaur. We furthermore explore the impacts of tooth position and cranial robustness on phytosaur microwear textures. We find subtle systematic texture differences between teeth from different positions along phytosaur tooth rows, which we interpret to be the result of different loading pressures experienced during food consumption, rather than functional partitioning of food processing along tooth rows. We find rougher microwear textures in morphologically robust taxa. This may be the result of seizing and processing larger prey items compared to those captured by gracile taxa, rather than dietary differences per se. We reveal relatively low dietary diversity between our study phytosaurs and that individual species show a lack of dietary specialization. Species are predominantly carnivorous and/or piscivorous, with two taxa exhibiting slight preferences for 'harder' invertebrates. Our results provide strong evidence for higher degrees of ecological convergence between phytosaurs and extant crocodilians than previously appreciated, furthering our understanding of the functioning and evolution of Triassic ecosystems. [ABSTRACT FROM AUTHOR]

Landmark-based Principal Component Analysis was performed on multiple phytosaur and crocodilian skulls. Multiple landmark points were selected defining suture points of bone tissues and regions of maximum or minimum curvature along the skull. Scatter plots of the principal component scores show that phytosaurs cluster according to their higher order taxonomic groups, and the convex hull polygons of the different clades occupy distinct morphospaces albeit with variable degrees of overlap. Disparity between the morphospaces of non-Mystriosuchinae parasuchids and Mystriosuchinae phytosaurs suggests marked differences in skull shape among basal and derived taxa. The vector deformation plots of phytosaur skulls showcase the evolution of skull shape from basal to advanced forms. The morphological changes imply evolution of the phytosaur skulls towards a wider and deeper snout, cage-like grip, tendency for increasing jaw strength, and faster-snapping action. In addition, heightening of the nostrils suggested that phytosaurs evolved into ambush predators, and increased their ability to remain submerged underwater with their nostrils high above the water surface, thereby enhancing their ability to ambush prey. The study supports prior assumptions of dietary preferences among the phytosaurs and maps the evolution and prevalence of cranial morphotypes, associated with such dietary preferences, across the different phytosaur clades. [ABSTRACT FROM AUTHOR]

Phytosaurs are a group of Upper Triassic semi‐aquatic archosauriform reptiles. Their variable skull morphology forms the foundation of our understanding of their relationships and paleoecology, while only a few studies have focused on demonstrating the existence of postcranial variation. The numbers of vertebrae in the sacrum are thought to vary from two, the plesiomorphic condition for archosauriforms, to three, with the addition of a sacralized dorsal (i.e., dorsosacral) vertebra. In this study, we demonstrate the presence of a sacralized first caudal (i.e., caudosacral) vertebra in a sacrum belonging to Machaeroprosopus mccauleyi. We rule out taphonomic distortion or pathology as explanations for the inclusion of this element in the sacrum, suggesting instead that it occurred through modifications of the same developmental processes that likely produced dorsosacral vertebrae in phytosaurs. Additionally, we show that a dorsosacral vertebra is common in phytosaur specimens from the Chinle Formation and Dockum Group of the southwestern United States and suggest that it may be widespread among phytosaurs. The addition of sacral vertebrae potentially aided adaptation to larger body sizes or more terrestrial lifestyles in certain taxa. [ABSTRACT FROM AUTHOR]

Abstract: 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. [ABSTRACT FROM AUTHOR]