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The effect of the Cretaceous-Paleogene (K-Pg) (formerly Cretaceous–Tertiary, K–T) mass extinction on avian evolution is debated, primarily because of the poor fossil record of Late Cretaceous birds. In particular, it remains unclear whether archaic birds became extinct gradually over the course of the Cretaceous or whether they remained diverse up to the end of the Cretaceous and perished in the K–Pg mass extinction. Here, we describe a diverse avifauna from the latest Maastrichtian of western North America, which provides definitive evidence for the persistence of a range of archaic birds to within 300,000 y of the K–Pg boundary. A total of 17 species are identified, including 7 species of archaic bird, representing Enantiornithes, Ichthyornithes, Hesperornithes, and an Apsaravis -like bird. None of these groups are known to survive into the Paleogene, and their persistence into the latest Maastrichtian therefore provides strong evidence for a mass extinction of archaic birds coinciding with the Chicxulub asteroid impact. Most of the birds described here represent advanced ornithurines, showing that a major radiation of Ornithurae preceded the end of the Cretaceous, but none can be definitively referred to the Neornithes. This avifauna is the most diverse known from the Late Cretaceous, and although size disparity is lower than in modern birds, the assemblage includes both smaller forms and some of the largest volant birds known from the Mesozoic, emphasizing the degree to which avian diversification had proceeded by the end of the age of dinosaurs.

Fig. 1. The phylogenetic distribution of ABO phenotypes and genotypes. Shown is a phylogenetic tree of primate species, with a summary of phenotypic/ genotypic information given in the first column, and the genetic basis for the A versus B phenotype provided in the second column (functionally important codons at positions 266 and 268 are in uppercase letters). See Dataset S1 for the source of information about phenotypes/genotypes. Only species with available divergence times are represented here (34 of 40). The phylogenetic tree is drawn to scale, with divergence times (on the x axis) in millions of years taken from ref. 29. OWM, Old World monkeys; NWM, New World monkeys. Under a model of convergent evolution, these data suggest that A is the ancestral allele, and a turnover (e.g., a neutral substitution) occurred on the branch leading to Old World monkeys. If instead, B were ancestral, all Old World monkeys would have had to serendipitously converge from ATG to TTG to encode a leucine, whereas all New World monkeys and hominoids would have had to converge to the CTG codon.

The fossil assemblages of the Late Cretaceous of North America are dominated by large-bodied dinosaur species. Associated skeletons of small dinosaurs are exceedingly rare, and small (<10 kg) carnivorous theropods have not previously been reported from these beds. Here, we describe a small dromaeosaurid from the 75-millionyear-old Dinosaur Park Formation of Alberta, Canada. Hesperonychus elizabethae gen. et sp. nov. is represented by a pelvic girdle from an animal weighing Ϸ1,900 g. Despite its size, the pubes and ilia are coossified, indicating that the animal was somatically mature. This is the smallest carnivorous, nonavian dinosaur known from North America. Phylogenetic analysis of Hesperonychus reveals that it is not closely related to previously described North American dromaeosaurids. Instead, Hesperonychus is a member of the dromaeosaurid clade Microraptorinae, a group containing the 4-winged Microraptor and the feathered Sinornithosaurus, both from the Lower Cretaceous Jehol Group of China. Hesperonychus is the youngest known member of this lineage, extending the temporal range of the clade by 45 million years, and it is the first microraptorine known from North America, providing further evidence for an affinity between the dinosaur faunas of North America and Asia. Study of fossil collections from the Dinosaur Park and Oldman formations of Alberta has revealed numerous isolated bones of small, basal dromaeosaurids, which are tentatively referred to Hesperonychus. These fossils suggest that small dromaeosaurids were a significant component of the carnivore community in this Late Cretaceous biota.Campanian ͉ Dinosaur Park Formation ͉ microraptorinae ͉ theropoda

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Historically, studies of pachycephalosaurs have recognized plesiomorphically flat-headed taxa and apomorphically domed taxa. More recently, it has been suggested that the expression of the frontoparietal dome is ontogenetic and derived from a flat-headed juvenile morphology. However, strong evidence to support this hypothesis has been lacking. Here we test this hypothesis in a large, stratigraphically constrained sample of specimens assigned to Stegoceras validum, the best known pachycephalosaur, using multiple independent lines of evidence including conserved morphology of ornamentation, landmark-based allometric analyses of frontoparietal shape, and cranial bone histology. New specimens show that the diagnostic ornamentation of the parietosquamosal bar is conserved throughout the size range of the sample, which links flat-headed specimens to domed S. validum. High-resolution CT scans of three frontoparietals reveal that vascularity decreases with size and document a pattern that is consistent with previously proposed histological changes during growth. Furthermore, aspects of dome shape and size are strongly correlated and indicative of ontogenetic growth. These results are complementary and strongly support the hypothesis that the sample represents a growth series of a single taxon. Cranial dome growth is positively allometric, proceeds from a flat-headed to a domed state, and confirms the synonymy of Ornatotholus browni as a juvenile Stegoceras. This dataset serves as the first detailed model of growth and variation in a pachycephalosaur. Flat-headed juveniles possess three characters (externally open cranial sutures, tuberculate dorsal surface texture, and open supratemporal fenestrae) that are reduced or eliminated during ontogeny. These characters also occur in putative flat-headed taxa, suggesting that they may also represent juveniles of domed taxa. However, open cranial sutures and supratemporal fenestrae are plesiomorphic within Ornithischia, and thus should be expected in the adult stage of a primitive pachycephalosaur. Additional lines of evidence will be needed to resolve the taxonomic validity of flat-headed pachycephalosaur taxa.

Snakes are a remarkably diverse and successful group today, but their evolutionary origins are obscure. The discovery of snakes with legs has shed light on the transition from lizards to snakes, but no snake has been described with four limbs. We describe a four-limbed snake from the Early Cretaceous (Aptian) Crato Formation of Brazil. The new snake has a serpentiform body plan with an elongate trunk, short tail, and large ventral scales suggesting characteristic serpentine locomotion, but retains small, prehensile limbs. Furthermore, the body proportions and reduced neural spines indicate a fossorial lifestyle, suggesting that snakes evolved from burrowing rather than marine ancestors. The structure of the hind limbs suggests that they may have functioned either to grasp prey or as claspers during mating. Hooked teeth, an intramandibular joint, a flexible spine capable of constricting prey, and the presence of vertebrate remains in the guts indicate that this species preyed on vertebrates, and that snakes made the transition to carnivory early in their history. Together with a diverse fauna of basal snakes from the Cretaceous of South America, Africa, and India, the new snake shows that crown Serpentes originated in Gondwana.

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