We highlight the historical and contemporary policies that govern paleontological research on federally recognized Native American lands. The United States has a long history of fossil dispossession from Indigenous Peoples, and federal policies surrounding the management of Native American lands (i.e., reservations), and the geological resources therein, have changed through time. These changes reflect shifting popular and political ideologies regarding Native American nations’ sovereignty and self-governance. As of 2022, the United States has a government-to-government relationship with federally recognized Tribal entities, but that has not always been the case. Historians have divided post-contact Native American federal policy into distinct eras: Colonial Times to 1820, Native American Removal and Reservation (1820–1887), Allotments and Attempted Assimilation (1887–1934), Reorganization and Preservation (1934–1953), Termination and Relocation (1953–1968), and Tribal Self-Determination (1968–present). Documentation of how the federal policies from each of these eras continue to impact current paleontological research is limited. We summarize major legislative actions, court cases, and historical events that have affected paleontological resource management in Native American territory. We use this historical context to identify federal policy gaps and highlight legal nuances associated with fossil collection and ownership, particularly given the importance of fossils to some Native Americans’ cultural patrimony. Finally, we explore how these gaps affect scientific research and highlight best practices for conducting paleontological research on vertebrate, invertebrate, and paleobotanical body and trace fossils using the CARE (Collective Benefit, Authority to Control, Responsibility, Ethics) Principles for Indigenous Data Governance (https://www.gida-global.org/care).

Evolutionary events may impact the geological carbon cycle via transient imbalances in silicate weathering, and such events have been implicated as causes of glaciations, mass extinctions, and oceanic anoxia. However, suggested evolutionary causes often substantially predate the environmental effects to which they are linked—problematic when carbon cycle perturbations must be resolved in less than a million years to maintain Earth's habitability. What is more, the geochemical signatures of such perturbations are recorded as they occur in widely distributed marine sedimentary rocks that have been densely sampled for important intervals in Earth history, whereas the fossil record—particularly on land—is governed by the availability of sedimentary basins that are patchy in both space and time, necessitating lags between the origination of an evolutionary lineage and its earliest occurrence in the fossil record. Here, we present a simple model of the impact of preservational filtering on sampling to show that an evolutionary event that causes an environmental perturbation via weathering imbalance should not appear earlier in the rock record than the perturbation itself and, if anything, should appear later rather than simultaneously. The Devonian Hangenberg glaciation provides an example of how evolutionary events might be more fruitfully considered as potential causes of environmental perturbations. Just as the last samplings of species lost in mass extinction are expected to come before the true environmental event, first appearance should be expected to postdate the geological expression of a lineage's environmental impact with important implications for our reading of Earth history.

The repeated return of tetrapods to aquatic life provides some of the best-known examples of convergent evolution. One comparison that has received relatively little focus is that of mosasaurids (a group of Late Cretaceous squamates) and archaic cetaceans (the ancestors of modern whales and dolphins), both of which show high levels of craniodental disparity, similar initial trends in locomotory evolution, and global distributions. Here we investigate convergence in skull ecomorphology during the initial aquatic radiations of these groups. A series of functionally informative ratios were calculated from 38 species, with ordination techniques used to reconstruct patterns of functional ecomorphospace occupation. The earliest fully aquatic members of each clade occupied different regions of ecomorphospace, with basilosaurids and early russellosaurines exhibiting marked differences in cranial functional morphology. Subsequent ecomorphological trajectories notably diverge: mosasaurids radiated across ecomorphospace with no clear pattern and numerous reversals, whereas cetaceans notably evolved toward shallower, more elongated snouts, perhaps as an adaptation for capturing smaller prey. Incomplete convergence between the two groups is present among megapredatory and longirostrine forms, suggesting stronger selection on cranial function in these two ecomorphologies. Our study highlights both the similarities and divergences in craniodental evolutionary trajectories between archaic cetaceans and mosasaurids, with convergences transcending their deeply divergent phylogenetic affinities.

Studies of insect herbivory on fossilized leaves tend to focus on a few, relatively simple metrics that are agnostic to the distribution of insect damage types among host plants. More complex metrics that link particular damage types to particular host plants have the potential to address additional ecological questions, but such metrics can be biased by sampling incompleteness due to the difficulty of distinguishing the true absence of a particular interaction from the failure to detect it—a challenge that has been raised in the ecological literature. We evaluate a range of methods for characterizing the relationships between damage types and host plants by performing resampling and subsampling exercises on a variety of datasets. We found that the components of beta diversity provide a more valid, reliable, and interpretable method for comparing component communities than do bipartite network metrics and that the rarefaction of interactions represent a valid, reliable, and interpretable method for comparing compound communities. Both beta diversity and rarefaction of interactions avoid the potential pitfalls of multiple comparisons. Finally, we found that the host specificity of individual damage types is challenging to assess. Whereas bipartite network metrics are sufficiently biased by sampling incompleteness to be inappropriate for fossil herbivory data, alternatives exist that are perfectly suitable for fossil datasets with sufficient sample coverage.

Developmental plasticity, where traits change state in response to environmental cues, is well studied in modern populations. It is also suspected to play a role in macroevolutionary dynamics, but due to a lack of long-term records, the frequency of plasticity-led evolution in deep time remains unknown. Populations are dynamic entities, yet their representation in the fossil record is a static snapshot of often isolated individuals. Here, we apply for the first time contemporary integral projection models (IPMs) to fossil data to link individual development with expected population variation. IPMs describe the effects of individual growth in discrete steps on long-term population dynamics. We parameterize the models using modern and fossil data of the planktonic foraminifer Trilobatus sacculifer. Foraminifera grow by adding chambers in discrete stages and die at reproduction, making them excellent case studies for IPMs. Our results predict that somatic growth rates have almost twice as much influence on population dynamics than survival and more than eight times more influence than reproduction, suggesting that selection would primarily target somatic growth as the major determinant of fitness. As numerous paleobiological systems record growth rate increments in single genetic individuals and imaging technologies are increasingly available, our results open up the possibility of evidence-based inference of developmental plasticity spanning macroevolutionary dynamics. Given the centrality of ecology in paleobiological thinking, our model is one approach to help bridge eco-evolutionary scales while directing attention toward the most relevant life-history traits to measure.

Bryozoans are active non-phototrophic biomineralizers that precipitate their calcareous skeletons in seawater. Carbonate saturation states varied temporally and spatially in Paleozoic oceans, and we used the Bryozoan Skeletal Index (BSI) to investigate whether bryozoan calcification was controlled by seawater chemistry in Paleozoic trepostome and cryptostome bryozoans. Our results show that cryptostome bryozoan genera were influenced by ocean chemistry throughout the Paleozoic and precipitated the most calcite at lower latitudes, where carbonate saturation states are generally higher, and less in midlatitudes, where carbonate will be relatively undersaturated. Trepostome bryozoan genera show a similar but weaker trend for the Ordovician to Devonian, suggesting that, like the cryptostomes, they were unable to metabolically overcome falling saturation states and simply precipitated less robust skeletons at higher latitudes. Carboniferous to Triassic trepostomes differ, however, and show a trend toward increased calcification at higher latitudes, indicating an ability to overcome unfavorable carbonate saturation states. Analysis of Permian trepostomes at the species level indicates this is most pronounced in the Southern Hemisphere, where calcification is matched by increased feeding capacity. It is proposed that this increased feeding capacity allowed trepostomes to metabolically overcome unfavorable carbonate saturation states. The differing responses of trepostome and cryptostome bryozoans to carbonate saturation states suggest that bryozoans should not be considered as a single group in marine extinctions linked to ocean chemistry changes. Likewise, it would suggest that modern stenolaemate and gymnolaemate bryozoans should be treated separately when considering their response to modern ocean chemistry changes.

The Cambrian saw a dramatic increase in metazoan diversity and abundance. Between-assemblage diversity (beta diversity) soared in the first three Cambrian stages, suggesting a rapid increase in the geodisparity of marine animals during the Cambrian radiation. However, it remains unclear how these changes scale up to first-order biogeographic patterns. Here we outline time-traceable provinces for marine invertebrates across the Cambrian period using a compositional network based on species-level fossil occurrence data. Results confirm an increase in regional differences of faunal composition and a decrease in by-species geographic distribution during the first three stages. We also show that general biogeography tends to be reshaped after global extinction pulses. We suggest that the abrupt biogeographic differentiation during the Cambrian radiation was controlled by a combination of tectonics, paleoclimate, and dispersal capacity changes.

The Asteropyginae Delo, 1935 is a group of phacopid trilobites in the family Acastidae Delo, 1935 that has served as the focus for several studies due to their distinctive morphologies and diversity. However, despite an interest in these characteristic morphologies, there have been no studies that have examined this group using morphometric techniques. Our investigation utilized both geometric morphometric and elliptical Fourier methods to quantify the morphology of cephalic sclerites of asteropyginid specimens representing wide taxonomic sampling of the clade. We constructed a phylomorphospace that shows temporal and spatial patterns of phenotypic evolution within the framework of a novel tip-dated phylogenetic tree generated using Bayesian inference. We recovered similar patterns in disparity regardless of the morphometric approach. Both analyses illustrated a marked expansion into morphospace throughout the temporal range of the clade, peaking in disparity in the Emsian and with European taxa exhibiting the highest disparity in glabellar morphospace. Additionally, glabellar shape showed low phylogenetic signal and no major patterns in phylomorphospace. This study highlights the utility of employing different methodologies to quantitatively explore the disparity of fossil taxa. It also illustrates some of the patterns of morphological change occurring during one of the final and major evolutionary radiations within Phacopida.

The rise of jawed vertebrates (gnathostomes) and extinction of nearly all jawless vertebrates (agnathans) is one of the most important transitions in vertebrate evolution, but the causes are poorly understood. Competition between agnathans and gnathostomes during the Devonian period is the most commonly hypothesized cause; however, no formal attempts to test this hypothesis have been made. Generally, competition between species increases as morphological similarity increases; therefore, this study uses the largest to date morphometric comparison of Silurian and Devonian agnathan and gnathostome groups to determine which groups were most and least likely to have competed. Five agnathan groups (Anaspida, Heterostraci, Osteostraci, Thelodonti, and Furcacaudiformes) were compared with five gnathostome groups (Acanthodii, Actinopterygii, Chondrichthyes, Placodermi, and Sarcopterygii) including taxa from most major orders. Morphological dissimilarity was measured by Gower's dissimilarity coefficient, and the differences between agnathan and gnathostome body forms across early vertebrate morphospace were compared using principal coordinate analysis. Our results indicate competition between some agnathans and gnathostomes is plausible, but not all agnathan groups were similar to gnathostomes. Furcacaudiformes (fork-tailed thelodonts) are distinct from other early vertebrate groups and the least likely to have competed with other groups.

Despite the rich fossil record of Neogene chondrichthyans (chimaeras, sharks, rays, and skates) from Europe, little is known about the macroevolutionary processes that generated their current diversity and geographical distribution. We compiled 4368 Neogene occurrences comprising 102 genera, 41 families, and 12 orders from four European regions (Atlantic, Mediterranean, North Sea, and Paratethys) and evaluated their diversification trajectories and paleobiogeographic patterns. In all regions analyzed, we found that generic richness increased during the early Miocene, then decreased sharply during the middle Miocene in the Paratethys, and moderately during the late Miocene and Pliocene in the Mediterranean and North Seas. Origination rates display the most significant pulses in the early Miocene in all regions. Extinction rate pulses varied across regions, with the Paratethys displaying the most significant pulses during the late Miocene and the Mediterranean and North Seas during the late Miocene and early Pliocene. Overall, up to 27% and 56% of the European Neogene genera are now globally and regionally extinct, respectively. The observed pulses of origination and extinction in the different regions coincide with warming and cooling events that occurred during the Neogene globally and regionally. Our study reveals complex diversity dynamics of Neogene chondrichthyans from Europe and their distinct biogeographic composition despite the multiple marine passages that connected the different marine regions during this time.

Notosuchia is a group of mostly terrestrial crocodyliforms. The presence of a prominent crest overhanging the acetabulum, slender straight-shafted long bones with muscular insertions close to the joints, and a stable knee joint suggests that they had an erect posture. This stance has been proposed to be linked to endothermy, because it is present in mammals and birds and contributes to the efficiency of their respiratory systems. However, a bone paleohistological study unexpectedly suggested that Notosuchia were ectothermic organisms. The thermophysiological status of Notosuchia deserves further analysis, because the methodology of the previous study can be improved. First, it was based on a relationship between red blood cell size and bone vascular canal diameter tested using 14 extant tetrapod species. Here we present evidence for this relationship using a more comprehensive sample of extant tetrapods (31 species). Moreover, contrary to previous results, bone cross-sectional area appears to be a significant explanatory variable (in addition to vascular canal diameter). Second, red blood cell size estimations were performed using phylogenetic eigenvector maps, and this method excludes a fraction of the phylogenetic information. This is because it generates a high number of eigenvectors requiring a selection procedure to compile a subset of them to avoid model overfitting. Here we inferred the thermophysiology of Notosuchia using phylogenetic logistic regressions, a method that overcomes this problem by including all of the phylogenetic information and a sample of 46 tetrapods. These analyses suggest that Araripesuchus wegeneri, Armadillosuchus arrudai, Baurusuchus sp., Iberosuchus macrodon, and Stratiotosuchus maxhechti were ectothermic organisms.

Here we report high-latitude stable isotope compositions of Maastrichtian fossil fish and marine reptiles (mainly mosasaurs) from Antarctica (64°S paleolatitude) and compare them with mid-paleolatitude samples from Argentine Patagonia (45°S). Disparities between the δ13C values of bony fish and marine reptiles correspond to differences in the foraging ground (distance from the shore and depth), while dramatically higher δ13C values (by 18‰) in shark enameloid cannot be explained through ecology and are here imputed to biomineralization. Comparison with extant vertebrates suggests that the diet alone can explain the offset observed between bony fish and mosasaurs; however, breath holding due to a diving behavior in mosasaurs may have had some impact on their δ13C values, as previously suggested. The δ18OPO4 values of the remains confirm a relatively stable, elevated body temperature for marine reptiles, meaning that they were thermoregulators. We calculated a water temperature of ~8°C for Antarctica from the fish δ18OPO4 values, warmer than present-day temperatures and consistent with the absence of polar ice sheets during the latest Maastrichtian. Our fish data greatly extend the latitudinal range of Late Cretaceous fish δ18OPO4 values and result in a thermal gradient of 0.4°C/1° of latitude when combined with literature data.