Morphology forms the most fundamental level of data in vertebrate palaeontology because it is through interpretations of morphology that taxa are identified, creating the basis for broad evolutionary and palaeobiological hypotheses. Assessing maturity is one of the most basic aspects of morphological interpretation and provides the means to study the evolution of ontogenetic changes, population structure and palaeoecology, life‐history strategies, and heterochrony along evolutionary lineages that would otherwise be lost to time. Saurian reptiles (the least‐inclusive clade containing Lepidosauria and Archosauria) have remained an incredibly diverse, numerous, and disparate clade through their ~260‐million‐year history. Because of the great disparity in this group, assessing maturity of saurian reptiles is difficult, fraught with methodological and terminological ambiguity. We compiled a novel database of literature, assembling >900 individual instances of saurian maturity assessment, to examine critically how saurian maturity has been diagnosed. We review the often inexact and inconsistent terminology used in saurian maturity assessment (e.g. ‘juvenile’, ‘mature’) and provide routes for better clarity and cross‐study coherence. We describe the various methods that have been used to assess maturity in every major saurian group, integrating data from both extant and extinct taxa to give a full account of the current state of the field and providing method‐specific pitfalls, best practices, and fruitful directions for future research. We recommend that a new standard subsection, ‘Ontogenetic Assessment’, be added to the Systematic Palaeontology portions of descriptive studies to provide explicit ontogenetic diagnoses with clear criteria. Because the utility of different ontogenetic criteria is highly subclade dependent among saurians, even for widely used methods (e.g. neurocentral suture fusion), we recommend that phylogenetic context, preferably in the form of a phylogenetic bracket, be used to justify the use of a maturity assessment method. Different methods should be used in conjunction as independent lines of evidence when assessing maturity, instead of an ontogenetic diagnosis resting entirely on a single criterion, which is common in the literature. Critically, there is a need for data from extant taxa with well‐represented growth series to be integrated with the fossil record to ground maturity assessments of extinct taxa in well‐constrained, empirically tested methods.

Cranial nerves are key features of the nervous system and vertebrate body plan. However, little is known about the anatomical relationships and ontogeny of cranial nerves in crocodylians and other reptiles, hampering understanding of adaptations, evolution, and development of special senses, somatosensation, and motor control of cranial organs. Here we share three dimensional (3D) models an of the cranial nerves and cranial nerve targets of embryonic, juvenile, and adult American Alligators (Alligator mississippiensis) derived from iodine‐contrast CT imaging, for the first time, exploring anatomical patterns of cranial nerves across ontogeny. These data reveal the tradeoffs of using contrast‐enhanced CT data as well as patterns in growth and development of the alligator cranial nervous system. Though contrast‐enhanced CT scanning allows for reconstruction of numerous tissue types in a nondestructive manner, it is still limited by size and resolution. The position of alligator cranial nerves varies little with respect to other cranial structures yet grow at different rates as the skull elongates. These data constrain timing of trigeminal and sympathetic ganglion fusion and reveal morphometric differences in nerve size and path during growth. As demonstrated by these data, alligator cranial nerve morphology is useful in understanding patterns of neurological diversity and distribution, evolution of sensory and muscular innervation, and developmental homology of cranial regions, which in turn, lead to inferences of physiology and behavior.

Highly branched dendritic structures are common in nature and often difficult to quantify and therefore compare. Cranial neurovascular canals, examples of such structures, are osteological correlates for somatosensory systems and have been explored only qualitatively. Adaptations of traditional stream‐ordering methods are applied to representative structures derived from computed tomography‐scan data. Applying these methods to crocodylian taxa, this clade demonstrates a shared branching pattern and exemplifies the comparative utility of these methods. Additionally, this pattern corresponds with current understanding of crocodylian sensory abilities and behaviors. The method is applicable to many taxa and anatomical structures and provides evidence for morphology‐based hypotheses of sensory and physiological evolution.

The examination of endocranial data of archosauriforms has led to advances on the evolution of body size, nerve pathways, and sensory abilities. However, much of that research has focused on bird-line archosaurs, resulting in a skewed view of Archosauria. Phytosauria, a hypothesized sister taxon to or early-branching member of Archosauria, provides a potential outgroup condition. Most previous phytosaur endocranial studies were executed without the use of modern technology and focused on derived members of Phytosauria. We present a comparative CT examination of the internal cranial anatomy of Wannia scurriensis, the most basal known parasuchid phytosaur. Wannia scurriensis shows some overall similarity with extant crocodylians and derived phytosaurs in general endocranial shape, a large hypophyseal fossa, and trigeminal (CN V) innervation, but as a whole, the endocast has noticeable differences to crocodylians and other phytosaurs. The pineal region is expanded dorsally as in other phytosaurs but also laterally (previously unrecognized). CN V exits the pons in a more dorsal position than in Parasuchus hislopi, Machaeroprosopus mccauleyi, or Smilosuchus gregorii. Wannia scurriensis also exhibits a larger hypophyseal fossa relative to brain size than observed in P. hislopi or S. gregorii, which may indicate more rapid growth. The well-preserved semicircular canals have lateral canals that are angled more anteroventrally than in derived phytosaurs. Extensive facial innervation from the large CN V indicates increased rostrum sensitivity and mechanoreceptive abilities as in Alligator mississippiensis. These endocranial similarities among phytosaurs and with Alligator indicate conserved ecological and functional results of an aquatic lifestyle, and highlight a need for further exploration of endocranial anatomy among Archosauriformes.

bearing assemblages from Texas using apomorphy-based identifications. PaleoBios, 35.ucmp_paleobios_39960.

Crocodylians evolved some of the most characteristic skulls of the animal kingdom with specializations for semiaquatic and ambush lifestyles, resulting in a feeding apparatus capable of tolerating high biomechanical loads and bite forces and a head with a derived sense of trigeminal‐nerve‐mediated touch. The mandibular symphysis accommodates these specializations being both at the end of a biomechanical lever and an antenna for sensation. Little is known about the anatomy of the crocodylian mandibular symphysis, hampering our understanding of form, function, and evolution of the joint in extant and extinct lineages. We explore mandibular symphysis anatomy of an ontogenetic series of Alligator mississippiensis using imaging, histology, and whole mount methods. Complex sutural ligaments emanating about a midline‐fused Meckel's cartilage bridge the symphysis. These tissues organize during days 37–42 of in ovo development. However, interdigitations do not manifest until after hatching. These soft tissues leave a hub and spoke‐like bony morphology of the symphyseal plate, which never fuses. Interdigitation morphology varies within the symphysis suggesting differential loading about the joint. Neurovascular canals extend throughout the mandibles to alveoli, integument, and bone adjacent to the symphysis. These features suggest the Alligator mandibular symphysis offers compliance in an otherwise rigid skull. We hypothesize a fused Meckel's cartilage offers stiffness in hatchling mandibles prior to the development of organized sutural ligaments and mineralized bone while offering a scaffold for somatic growth. The porosity of the dentaries due to neurovascular tissues likely allows transmission of sensory and proprioceptive information from the surroundings and the loaded symphysis. Anat Rec, 302:1696–1708, 2019. © 2019 American Association for Anatomy

The study of the rostral neurovascular system using CT scanning has shed new light on phylogenetic and palaeobiological reconstructions of many extinct tetrapods. This research shows a detailed description of the rostral neurovascular canals of Tyrannosaurus rex including the nasal, maxillary (dorsal alveolar), and mandibular (ventral alveolar) canals. Extensive comparisons with published descriptions show that the pattern of these canals in Tyrannosaurus is not unusual for a non-avian theropod. As in the non-avian theropod Neovenator, the maxillary canal shows several anastomoses of its branches. Differences from the plesiomorphic sauropsid condition are concentrated within the canal for the maxillary neurovasculature, which is primitively horizontal, tubular, and connected to a single row of supralabial foramina, whereas in Tyrannosaurus the main trunk of the canal is oriented more obliquely and dorsally displaced to give room to the deep tooth alveolae. As a result, the lateral branches that provide innervation and blood supply to the skin are dorsoventrally elongated compared to non-theropod taxa, and multiple rows of supralabial foramina are present. An overview of the literature suggests that the evolution of the trigeminal canals among sauropsids only weakly supports previous hypotheses of crocodile-like facial sensitivity in non-avian theropods (except, maybe, in semiaquatic taxa). More systematic studies of the rostral neurovascular canals in non-avian theropods may help answer the question of whether lips were present or not.

Rauisuchids are large (2–6 m in length), carnivorous, and quadrupedal pseudosuchian archosaurs closely related to crocodylomorphs. Though geographically widespread, fossils of this clade are relatively rare in Late Triassic assemblages. The middle Norian (∼212 Ma) Hayden Quarry of northern New Mexico, USA, in the Petrified Forest Member of the Chinle Formation, has yielded isolated postcranial elements and associated skull elements of a new species of rauisuchid. Vivaron haydeni gen. et. sp. nov. is diagnosed by the presence of two posteriorly directed prongs at the posterior end of the maxilla for articulation with the jugal. The holotype maxilla and referred elements are similar to those of the rauisuchid Postosuchus kirkpatricki from the southwestern United States, but V. haydeni shares several maxillary apomorphies (e.g., a distinct dropoff to the antorbital fossa that is not a ridge, a straight ventral margin, and a well defined dental groove) with the rauisuchid Teratosaurus suevicus from the Norian of Germany. Despite their geographic separation, this morphological evidence implies a close phylogenetic relationship between V. haydeni and T. suevicus. The morphology preserved in the new Hayden Quarry rauisuchid V. haydeni supports previously proposed and new synapomorphies for nodes within Rauisuchidae. The discovery of Vivaron haydeni reveals an increased range of morphological disparity for rauisuchids from the low-paleolatitude Chinle Formation and a clear biogeographic connection with high paleolatitude Pangea.