Mario Bronzati

Pterosaurs were the first vertebrates to achieve powered flight, a result of various unique anatomical adaptations, and significant morphological diversity throughout their evolutionary history. Although the pterosaurs body structure was specialized for powered flight, the clade exhibited great disparity from its origins, with later evolution giving rise to multiple phylogenetic lineages and a wide range of body sizes, from small forms such as Anurognathus ammoni to truly giant species like Quetzalcoatlus northropi . This variation led to distinct flight strategies within the group. Here, we assess allometry in the skeletal elements of Rhamphorhynchus muensteri in comparison with Eupterodactyloidea and Euctenochasmatia, examining their implications for paleoecology and flight capacity. The analysis included 127 specimens and assessed 13 skeletal variables using statistical methods, principal components analysis (PCA), and standardized major analysis (SMA). The results reveal differences in size–shape trajectories and functional adaptations related to activity flight. R. muensteri exhibits a trend of negative allometry (PCRW/body, humerus, radius/ulna, metacarpal IV, and femur), indicating distinct allometric scaling patterns and flight style. These patterns suggest behavior and ecological differences, as well differing flight capabilities between R. muensteri likely relied on active flapping flight interspersed with gliding, whereas other taxa may have exhibited greater migratory adaptations within Eupterodactyloidea, and a greater dependence on flapping flight in Euctenochasmatia. The negative allometry in R. muensteri suggests a flight style characterized by early flight capability (precocial flight), whereas Eupterodactyloidea showed positive allometry and Euctenochasmatia isometry. Additionally, the study highlights how allometric patterns influence pterosaur phylogeny, underscoring the importance of incorporating them into future analysis.

There is a growing consensus that pterosaurs and the flightless Lagerpetidae are closely related. This relationship is supported by apomorphies throughout the skeleton, including endocranial character states such as a well‐developed floccular fossa and a tall anterior semicircular canal. Our knowledge of lagerpetid anatomy has been improved by recent discoveries. Among them, the Brazilian record plays a significant role, having produced two described species, Ixalerpeton polesinensis and Venetoraptor gassenae , and several more fragmentary specimens. In this study, we used an x‐ray micro‐computed tomographic scan to describe the endocranial anatomy of the holotype of Venetoraptor gassenae . The endocranial anatomy of Venetoraptor gassenae is similar in shape to that of other described lagerpetids, and we reach the following conclusions: (1) in pterosaurs, the metotic foramen exits posteriorly, whereas in lagerpetids and dinosauromorphs it exits through the lateral wall of the braincase; and (2) Venetoraptor gassenae is unique among lagerpetids in having only one exit for cranial nerve XII, expanding its differential diagnosis. These differences highlight that the braincase anatomy of lagerpetids is aligned with the anatomical disparity observed in the group. Finally, we discuss why future studies should focus on comprehending patterns of braincase pneumaticity in avemetatarsalians.

A complete morphological description of Dakosaurus maximus (Crocodyliformes: Thalattosuchia) with further insights into their palaeoecology

Whereas mammals are characterized by the presence of three middle ear ossicles, reptiles have only one, the columella (stapes). Nevertheless, there is a great diversity of columellar anatomy among sauropsids, especially in the unique and cartilaginous “extracolumella”‐portion. Molecular studies revealed the “columella” of chicken and quails to be formed within the second pharyngeal arch, although conflicting evidence exists for the columellar footplate and distal parts of the columella in these birds. We studied columellar development in four turtles, one lizard, and one caiman species and argue, using early blastematous stages, that, distally, the so‐called “extracolumella” in turtles is mainly of quadrate, that is, first pharyngeal arch origin. Differently, the dorsal aspect of the “extracolumella” of the lizard and a part of the “dorsal columella process” of the caiman are likely quadrate‐derived. This indicates only a partial homology of the distal columellar compartments among reptiles. Moreover, we observed in most species that, at early stages, the footplate differentiates from the otic capsule, which confirms widespread experimental findings of mesodermal cells contributing to the proximal part of the columella. We provide a hypothetical framework for the changes in the columella and quadrate morphology in reptilian evolution. Originally, as evidenced by the fossil record, the columella served as a stabilizing brace between the quadrate and braincase. Associated with changes in the feeding mode of late Permian taxa, the quadrate was integrated along the stress flows from biting, and in early development part of the quadrate differentiated to differently contribute to the distal part of the “columella‐complex,” which now contacts the tympanic membrane. In addition, part of the original otic capsule contributes to the footplate of the mobile columella, providing a connection with the inner ear.

Peirosauridae (Crocodyliformes, Notosuchia) is one of the fossil lineages of crocodyliforms ubiquitous in the Cretaceous deposits of the Bauru Basin. Here, we describe a new species of a longirostrine Peirosauridae from the Adamantina Formation (Bauru Basin, Late Cretaceous). The specimen consists of a partially preserved skull with a cranial roof, interorbital region, and fragments of the posterior portion of the rostrum, including the prefrontal and lacrimal; left hemimandible, with 14 alveoli and 12 teeth; and a single cervical rib fragment. The specimen is associated with Peirosauridae by three cranial synapomorphies, and it can be assigned to a new genus and species by presenting seven cranial and one tooth apomorphies. To clarify the position of the new taxon, an updated phylogenetic analysis was performed with increased sampling of taxa of Notosuchia, especially Peirosauridae, and phylogenetically relevant characters. Our results indicated the monophyly of Peirosauridae, formed by two main lineages, the oreinirostral and presumably terrestrial Peirosaurinae and the longirostrine and presumably semi‐aquatic Pepesuchinae. The recovering of both lineages as distinct entities was also reinforced through a morphospace analysis. Pepesuchinae were notable by exploring a position of the morphospace not explored by any other Notosuchia. Their longer rostra and the assumption of them being gradually specialized to aquatic habits reflects the unique diversity of these crocodyliforms through the Cretaceous deposits of South America and Africa.

The anatomy of the braincase and associated soft tissues of the lagerpetid Dromomeron gregorii (Archosauria: Avemetatarsalia) from the Late Triassic of the United States is here described. This corresponds to the first detailed description of cranial materials of Lagerpetidae, an enigmatic group of Late Triassic (c. 236–200 Million years ago) animals that are the closest known relatives of pterosaurs, the flying reptiles. The braincase of D. gregorii is characterized by the presence of an anteriorly elongated laterosphenoid and a postparietal, features observed in stem‐archosaurs but that were still unknown in early members of the avian lineage of archosaurs. Using micro‐computed tomography (CT‐scan data), we present digital reconstructions of the brain and endosseous labyrinth of D. gregorii. The brain of D. gregorii exhibits a floccular lobe of the cerebellum that projects within the space of the semicircular canals. The semicircular canals are relatively large when compared to other archosauromorphs, with the anterior canal exhibiting a circular shape. These features of the sensory structures of D. gregorii are more similar to those of pterosaurs than to those of other early avemetatarsalians. In sum, the braincase anatomy of D. gregorii shows a combination of plesiomorphic and apomorphic features in the phylogenetic context of Archosauria and suggests that the still poorly understood early evolution of the braincase in avemetatarsalians is complex, with a scenario of independent acquisitions and losses of character states.

Hanson et al . (Research Articles, 7 May 2021, p. 601) claim that the shape of the vestibular apparatus reflects the evolution of reptilian locomotion. Using biomechanics, we demonstrate that semicircular canal shape is a dubious predictor of semicircular duct function. Additionally, we show that the inference methods used by Hanson et al . largely overestimate relationships between semicircular canal shape and locomotion.

Pseudosuchia includes crocodylians, plus all extinct species more closely related to them than to birds. They appeared around 250 million years ago and have a rich fossil history, showing extinct diversity that exceeds that of their living members1-4. Recently, Stockdale & Benton5 presented analyses of a new dataset of body size estimates spanning the entire evolutionary history of this group. They quantified patterns of average body size, body size disparity through time, and rates of evolution along phylogenetic lineages. Their results suggest that pseudosuchians exhibited considerable variation in rates of body size evolution, for which they provided various group-specific explanations and asserted the importance of climatic drivers. This differs from two recent studies that analysed a substantial portion of pseudosuchian body size evolution and proposed that adaptation to aquatic life, a biological innovation of some subgroups, was the main driver of body size evolution, with patterns of disparity also being influenced by size-dependent extinction risk6,7. Here we show that the analytical results of Stockdale & Benton5 are strongly influenced by a methodological error in their body size index. Specifically, that they chose not to log-transform measurement data prior to analyses.