Ceratopsian dinosaurs underwent great changes, including a shift of locomotion mode, enlarged horns and frills, and increased body size. These changes occur alongside the evolution of endocranial morphology and physiology such as the size and shape of the flocculus, hearing range, olfactory ratio, and the reptile encephalization quotient (REQ). However, the evolution of endocranial structures in early ceratopsians is still unclear because of a lack of information on the earliest ceratopsians. Here, we reconstructed the endocasts of three early-diverging ceratopsians including the Late Jurassic Yinlong, and the Early Cretaceous Liaoceratops and Psittacosaurus. These ceratopsians display obvious flocculi, large and separate olfactory bulbs, long and high anterior semicircular canals, and relatively long cochlear ducts. In the evolution of the earliest ceratopsians to early neoceratopsians, changes include the increasing size of the flocculus (which is reduced or absent in late-diverging ceratopsids), the attenuation of the semicircular canals, and the heightening of the anterior semicircular canal (which is shortened in late-diverging ceratopsids). The endocranial structures suggest early-diverging ceratopsians had a higher olfactory acuity and were adapted to hearing higher frequencies than late-diverging ceratopsians. Furthermore, the REQ suggests that Yinlong and Psittacosaurus were more highly encephalized than late-diverging ceratopsians and most extant reptiles. The angle of the lateral semicircular canal suggests that heads in ceratopsians display a transition from a forward posture to a more downward posture. Our new findings are significant for understanding the physiological changes during ceratopsian evolution and also have implications for the evolution of physiology in extant tetrapods.

Understanding cranial sutures and how they relieve and dissipate stress is essential to assess their role in cranial biomechanics and to develop highly accurate predictive models. This involves examining how ontogeny affects cranial sutures, as well as their morphology and function, and how these changes through time may impact essential biomechanical loadings such as chewing or direct biting. In this work, we study the cranial sutures of Crocodylus niloticus in detail using contact elements under finite element analysis. Contact elements permit the creation of a physical relationship between two bones that are in contact and even the configuration of these relationships, for example, in terms of movement or flexibility. The definition of bone contacts may require linear and/or nonlinear computational solutions to attain higher accuracy. Herein, skull geometry is tested to determine how bones may be altered by different types of contacts under various conditions. As predicted, the absence of sutures or cranial kinesis leads to a reduction in stress distribution across the skull, whereas sutures and cranial kinesis help the skull relieve stress and prevent certain bones from sustaining high stress levels. The type of contact used in individual sutures has a significant effect on model outcomes. Additionally, feeding behaviors significantly impact cranial biomechanics, reflecting the influence of other variables that may be applied to the models. As highlighted by the results, in order to obtain accurate results when analyzing fossil taxa, the nature of the cranial sutures should be taken into account. Therefore, developing predictive models based on living taxa is invaluable, because it facilitates the study of extinct taxa for which there is a lack of information on the fibrous joints due to poor or no preservation in the fossil record.

The Late Triassic conodont species Mockina ex gr. carinata and Mockina ex gr. englandi were exceptionally prevalent among the marine fauna of the Panthalassan realm from the middle Norian through to the Rhaetian. Leading into the complete extinction of conodonts near the Triassic/Jurassic boundary, a significant turnover event occurred in conodont fauna across the Norian/Rhaetian boundary (NRB), with the pectiniform elements of common Rhaetian genera from Tethys exhibiting minimal or absent platforms. This intergeneric trend of platform reduction is not as evident in Panthalassa, where these genera are very rare, but morphometric analyses of M. ex gr. carinata and M. ex gr. englandi specimens from across the Canadian Cordillera demonstrate that comparable shifts in morphology occurred intraspecifically in Panthalassa across the NRB, confirming the global extent of these trends. Pectiniform elements of M. ex gr. carinata display a sequential reduction of platform width from the middle Norian to late Norian to Rhaetian, whereas pectiniform elements of M. ex gr. englandi display a reduction of platform width only from the late Norian to Rhaetian. Specimens of both species that have a mid-platform length to breadth ratio greater than 3:1 are restricted to the Rhaetian. Specimens from the Kennecott Point section on Haida Gwaii, British Columbia, demonstrate that this morphological shift occurred somewhat later than other biostratigraphic proxies for the NRB. The global trend of platform width reduction in many conodont pectiniform elements may reflect a change in primary diet away from hard food sources, perhaps suggesting some degree of carbonate biomineralization suppression beginning around the NRB. This interpretation would support CO2 outgassing as the causal mechanism of the environmental disturbance at the NRB and identify the NRB as a significant turning point for Late Triassic ecosystems, marking the beginning of a protracted, multiphase end-Triassic mass extinction.

Crocodylomorpha is a large and diverse clade with a long evolutionary history now restricted to modern crocodilians. Tethysuchia is a less-inclusive clade of semi-amphibious taxa that crossed two biological crises: the second Oceanic Anoxic Event (OAE 2) and the Cretaceous/Paleogene (K/Pg) crisis. Numerous studies have sought to find the driving factors explaining crocodylomorph evolution, producing contradictory conclusions. Studies of included groups may be useful. Here, we study factors driving tethysuchian evolution using phylogenetically informed statistical analyses. First, we tested the phylogenetic structure of tethysuchian extinction at the OAE 2 and K/Pg crises. We then used phylogenetic comparative methods to test the influence of intrinsic (body size, snout proportion) and extrinsic (temperature, paleolatitude) factors on the evolution of tethysuchian diversity at the OAE 2 and the K/Pg crises. Finally, we tested whether temperature influenced the evolution of body size. We conclude that (1) extinction was not random in regard to phylogeny for Tethysuchia at the OAE 2 and K/Pg crises; (2) while an important tethysuchian turnover follows OAE 2, the K/Pg crisis was followed by an explosion in diversity of tethysuchians, probably linked to the colonization of emptied ecological niches; (3) tethysuchians lived in warmer environments after the OAE 2 crisis, possibly because of both global warming and latitudinal distribution shifts; (4) there is a significant change of snout proportion after the OAE 2 and the K/Pg crises, likely caused by niche partitioning; and (5) there is a positive correlation between body size and temperature, possibly because of a longer growth season.

The unique body plan of frogs (Lissamphibia: Anura) has been largely conserved from at least 200 Myr, and its evolution from a more generalized tetrapod condition is still poorly understood, in part due to the scarce early fossil record of Salientia, the anuran total-group. The origin of the anuran Bauplan has been classically explained as an adaptation to jumping, but recent studies incorporating new data in a phylogenetic context have challenged the popular jumping hypothesis. Here we revisit and test this hypothesis from a paleobiological perspective by integrating limb data from a wide range of extant and fossil frogs. We first explored the evolution of limb proportions from the Jurassic to the Paleogene to understand when the present limb diversity originated and whether, and to what extent, limb proportions have been conserved over the last 200 Myr. We then inferred the locomotor capabilities of extinct species by phylogenetic flexible discriminant analysis, and from these inferences, we studied the locomotor diversity of frogs over geological time and reconstructed the ancestral state for frog-like salientians. The evolution of limb proportions is characterized by an early diversification that was underway in the Jurassic, followed by a repeated convergence over a limited area of the morphospace that was already explored by the Early Cretaceous. In agreement with this early limb diversity, the Jurassic stem species were also locomotory diverse, and their inferred locomotor modes do not support the jumping hypothesis. We propose that the patterns found herein of repeated convergent evolution of both limb proportions and locomotor capabilities over geological time hamper any attempt to confidently infer the ancestral locomotion mode and, it therefore might be time to start focusing on other hypotheses on the origin of the anuran Bauplan that are not related to locomotion.

Theropods are obligate bipedal dinosaurs that appeared 230 Ma and are still extant as birds. Their history is characterized by extreme variations in body mass, with gigantism evolving convergently between many lineages. However, no quantification of hindlimb functional morphology has shown whether these body mass increases led to similar specializations between distinct lineages. Here we studied femoral shape variation across 41 species of theropods (n = 68 specimens) using a high-density 3D geometric morphometric approach. We demonstrated that the heaviest theropods evolved wider epiphyses and a more distally located fourth trochanter, as previously demonstrated in early archosaurs, along with an upturned femoral head and a mediodistal crest that extended proximally along the shaft. Phylogenetically informed analyses highlighted that these traits evolved convergently within six major theropod lineages, regardless of their maximum body mass. Conversely, the most gracile femora were distinct from the rest of the dataset, which we interpret as a femoral specialization to “miniaturization” evolving close to Avialae (bird lineage). Our results support a gradual evolution of known “avian” features, such as the fusion between lesser and greater trochanters and a reduction of the epiphyseal offset, independent from body mass variations, which may relate to a more “avian” type of locomotion (more knee than hip driven). The distinction between body mass variations and a more “avian” locomotion is represented by a decoupling in the mediodistal crest morphology, whose biomechanical nature should be studied to better understand the importance of its functional role in gigantism, miniaturization, and higher parasagittal abilities.

Numerous, high-quality reproduction-related oviraptorosaur fossils have been described. However, oviraptorosaur-style nests are unknown among extant animals, and their curious construction makes nesting behavior difficult to interpret. Experiments were undertaken to better understand oviraptorosaur nesting strategies. A surrogate was constructed and placed atop mock-oviraptorosaur nests built from sand and 36 infertile emu eggs (as Macroolithus approximations) arranged according to the most current nest reconstructions. Thermometers, placed within each egg and throughout the experimental area, recorded energy flow from the surrogate dinosaur into the nesting microenvironment. One experiment examined a basic open nest warmed from above; the second, a fully buried clutch warmed from above; and the third, a nest open like the first but with heating elements (representing hindlimbs) extending down into the nest. It was found that egg temperatures in each scenario surpassed ambient temperatures without requiring excessive energy input. Final clutch temperatures were below most avian values, closer to crocodilian incubation, but are likely conservative, considering experimental parameters. These results may support the idea that an oviraptorosaur could use adult-generated energy to warm a clutch above ambient conditions. Additionally, egg tiers would be warmer and more uniform in temperature if heated by elements within the nest, such as hindlimbs, instead of solely from above. Results from the second experiment indicate that an endothermic adult could possibly warm a clutch fully buried beneath itself despite a barrier. Although not likely a behavior exhibited by oviraptorosaurs, such results suggest an important evolutionary step bridging guarded subterranean eggs and contact-incubated subaerial eggs.

Electron backscatter diffraction (EBSD) has been widely used in recent studies of eggshells for its convenience in collecting in situ crystallographic information. China has a wide variety of dinosaur eggshells, although nearly none have been studied with this technique. Elongatoolithid eggs include many oogenera, although the microstructural differences of some were not highly appreciated, leading to several parataxonomic problems. In this paper, we surveyed seven elongatoolithid oogenera in China using EBSD in order to acquire more information about their microstructural variation. It is shown in this paper that in some elongatoolithid eggshells, scaly calcite grains that form the squamatic ultrastructure are not the only form of calcite in the continuous layer. Large columnar grains separated by high-angled grain boundaries and slender subgrains separated by radially arranged low-angled grain boundaries could exist in certain areas of the eggshells such as Macroolithus and Macroelongatoolithus. This paper discusses the criteria for identifying squamatic ultrastructure and proposes type I (rich in rugged high-angled grain boundaries) and type II (rich in both rugged high- and low-angled grain boundaries) squamatic ultrastructures. A pathological layer is found in Undulatoolithus pengi. An external zone is identified in the eggshell of Heishanoolithus changii, which does not support its position within the oofamily Elongatoolithidae. We argue that Paraelongatoolithus no longer belongs to Elongatoolithidae based on a combination of reticulated ornamentation, columnar continuous layer, and acicular mammillae. The high structural variation in elongatoolithid eggshells also implies that it may be inappropriate to relate all previous elongatoolithid eggshells to oviraptorosaurs and assume they are non-monophyletic.

Fossil bones were once living tissues that demanded internal blood perfusion in proportion to their metabolic requirements. Metabolic rates were primarily associated with bone growth (modeling) in the juvenile stages and with alteration and repair of existing bone affected by weight bearing and locomotion (remodeling) in later stages. This study estimates blood flow rates to the tibia shafts of the Late Cretaceous hadrosaurid Maiasaura peeblesorum, based on the size of the primary nutrient foramina in fossil bones. Foramen size quantitatively reflects arterial size and hence blood flow rate. The results showed that the bone metabolic intensity of juveniles (ca. 1 year old) was greater than fourfold higher than that of 6- to 11-year-old adults. This difference is much greater than expected from standard metabolic scaling and is interpreted as a shift from the high metabolic demands for primary bone modeling in the rapidly growing juveniles to a lower metabolic demand of adults to remodel their bones for repair of microfractures accumulated during locomotion and weight bearing. Large nutrient foramina of adults indicate a high level of cursorial locomotion characteristic of tachymetabolic endotherms. The practical value of these results is that juvenile and adult stages should be treated separately in interspecific analyses of bone perfusion in relation to body mass.

Apicobasal ridges are longitudinal ridges of enamel that are particularly common in several clades of aquatic-feeding predatory amniotes, including Plesiosauria, Ichthyosauria, Mosasauridae, Crocodylia, and Spinosauridae, as well as some early members of Cetacea. Although the repeated evolution of these dental ridges in unrelated clades suggests an adaptive benefit, their primary function in feeding is debated. Hypothesized functions range from increasing tooth strength to improving prey puncture or removal efficiency, but these have never been quantitatively tested. This study utilizes finite element analysis (FEA) to assess the impact of apicobasal ridges upon tooth crown strength in aquatic-feeding amniotes. Drawing on morphometric data from fossilized tooth crowns, a set of digital models was constructed to calculate the performance of smooth and ridged tooth variants under simulated bite force loadings. The similarities in overall stress distribution patterns across models of the same tooth shape, regardless of the presence or morphology of ridges, indicate that apicobasal ridges have little impact on stress reduction within the tooth crown. Ultimately, these findings suggest that apicobasal ridges have a minimal role in improving crown strength and form a framework for future research into the remaining hypotheses.

Body size has a long history of study in paleobiology and underlies many important phenomena in macroevolution. Body-size patterns in the fossil record are often examined by utilizing size data alone, which hinders our ability to describe the biological meaning behind size change on macroevolutionary timescales. Without data reflecting the biological and geologic factors that drive size change, we cannot assess its mechanistic underpinnings.

Existing frameworks for studying ontogeny and phylogeny can remedy this problem, particularly the classic age–size–“shape” space originally developed for studies of heterochrony. When evaluated based on metrics for age, size, and phenotype in populations, proposed mechanisms for size change can be outlined theoretically and tested empirically in the record. Using this framework, we can compare ontogenetic trajectories within and between species and determine how changes in size emerge. Here, we outline ontogenetic mechanisms for evolutionary size change, such as heterochrony, as well as how geologic factors can drive apparent, non-biological size change (e.g., taphonomic size sorting).

To demonstrate the utility of this framework in actual paleobiological problems, we apply it to the Lilliput effect, a compelling and widely documented pattern of size decrease during extinction events. However, little is known about the mechanisms underlying this pattern. We provide a brief history of the Lilliput effect and refine its definition in a framework that can be mechanistically tested. Processes that likely produce Lilliput effects include allometric and sequence repatterning (including heterochrony) and evolutionary size-selective sorting. We describe these mechanisms and highlight relevant examples of the Lilliput effect for which feasible empirical tests are possible.

During the late Miocene and early Pliocene (latest Hemphillian, Hh4 interval, 5.7 to 4.75 Ma) a distinctive suite of four species of extinct horses (Family Equidae) were widespread in North America. This includes Nannippus aztecus, Neohipparion eurystyle, Astrohippus stocki, and Dinohippus mexicanus. In Florida, two additional equid species, Pseudhipparion simpsoni and Cormohipparion emsliei, are also typically found at Hh4 localities. Here we compare horses from four Hh4 Florida fossil sites, including three from the Bone Valley mines and a fourth from the recently discovered Montbrook site. Two of these sites have all six expected species, one has five species, and one has only four species present. To explain these differences, we used species counts from research databases and rarefaction simulation to clarify the relative abundances, species richness, and occurrences of these horses from these four sites. The Palmetto Mine (Agrico) site, with five equid species, appears to lack the sixth species owing to ecological reasons. This is different from Montbrook, the site with only four of the six species. Results indicate that Montbrook is likely lacking two missing equid species for a couple of reasons: sampling bias and biological/ecological causes. Our results demonstrate that sampling biases can account for observed equid species richness when the overall abundance of certain equid species is low. Nevertheless, other factors, including ecology and with sufficient resolution, perhaps also time, may also explain the distribution and occurrences of individual species at these and other fossil sites. In a broader perspective, analyses such as this example provide an opportunity to address a persistent challenge in paleontology, that is, how do we explain absences of extinct taxa from the fossil record?

Scaling fluctuation analyses of marine animal diversity and extinction and origination rates based on the Paleobiology Database occurrence data have opened new perspectives on macroevolution, supporting the hypothesis that the environment (climate proxies) and life (extinction and origination rates) are scaling over the “megaclimate” biogeological regime (from ≈1 Myr to at least 400 Myr). In the emerging picture, biodiversity is a scaling “crossover” phenomenon being dominated by the environment at short timescales and by life at long timescales with a crossover at ≈40 Myr. These findings provide the empirical basis for constructing the Fractional MacroEvolution Model (FMEM), a simple stochastic model combining destabilizing and stabilizing tendencies in macroevolutionary dynamics, driven by two scaling processes: temperature and turnover rates.

Macroevolution models are typically deterministic (albeit sometimes perturbed by random noises) and are based on integer-ordered differential equations. In contrast, the FMEM is stochastic and based on fractional-ordered equations. Stochastic models are natural for systems with large numbers of degrees of freedom, and fractional equations naturally give rise to scaling processes.

The basic FMEM drivers are fractional Brownian motions (temperature, T) and fractional Gaussian noises (turnover rates, E+) and the responses (solutions), are fractionally integrated fractional relaxation noises (diversity [D], extinction [E], origination [O], and E− = O − E). We discuss the impulse response (itself representing the model response to a bolide impact) and derive the model's full statistical properties. By numerically solving the model, we verified the mathematical analysis and compared both uniformly and irregularly sampled model outputs with paleobiology series.

Strata of the Ediacaran Period (635–538.8 Ma) yield the oldest known fossils of complex, macroscopic organisms in the geologic record. These “Ediacaran-type” macrofossils (known as the Ediacaran biota) first appear in mid-Ediacaran strata, experience an apparent decline through the terminal Ediacaran, and directly precede the Cambrian (538.8–485.4 Ma) radiation of animals. Existing hypotheses for the origin and demise of the Ediacaran biota include: changing oceanic redox states, biotic replacement by succeeding Cambrian-type fauna, and mass extinction driven by environmental change. Few studies frame trends in Ediacaran and Cambrian macroevolution from the perspective of the sedimentary rock record, despite well-documented Phanerozoic covariation of macroevolutionary patterns and sedimentary rock quantity. Here we present a quantitative analysis of North American Ediacaran–Cambrian rock and fossil records from Macrostrat and the Paleobiology Database. Marine sedimentary rock quantity increases nearly monotonically and by more than a factor of five from the latest Ediacaran to the late Cambrian. Ediacaran–Cambrian fossil quantities exhibit a comparable trajectory and have strong (rs > 0.8) positive correlations with marine sedimentary area and volume flux at multiple temporal resolutions. Even so, Ediacaran fossil quantities are dramatically reduced in comparison to the Cambrian when normalized by the quantity of preserved marine rock. Although aspects of these results are consistent with the expectations of a simple fossil preservation–induced sampling bias, together they suggest that transgression–regression and a large expansion of marine shelf environments coincided with the diversification of animals during a dramatic transition that is starkly evident in both the sedimentary rock and fossil records.