Microraptor gui , a four-winged dromaeosaur from the Early Cretaceous of China, provides strong evidence for an arboreal-gliding origin of avian flight. It possessed asymmetric flight feathers not only on the manus but also on the pes. A previously published reconstruction shows that the hindwing of Microraptor supported by a laterally extended leg would have formed a second pair of wings in tetrapteryx fashion. However, this wing design conflicts with known theropod limb joints that entail a parasagittal posture of the hindlimb. Here, we offer an alternative planform of the hindwing of Microraptor that is concordant with its feather orientation for producing lift and normal theropod hindlimb posture. In this reconstruction, the wings of Microraptor could have resembled a staggered biplane configuration during flight, where the forewing formed the dorsal wing and the metatarsal wing formed the ventral one. The contour feathers on the tibia were positioned posteriorly, oriented in a vertical plane for streamlining that would reduce the drag considerably. Leg feathers are present in many fossil dromaeosaurs, early birds, and living raptors, and they play an important role in flight during catching and carrying prey. A computer simulation of the flight performance of Microraptor suggests that its biplane wings were adapted for undulatory “phugoid” gliding between trees, where the horizontal feathered tail offered additional lift and stability and controlled pitch. Like the Wright 1903 Flyer, Microraptor , a gliding relative of early birds, took to the air with two sets of wings.
New plesiosaur remains from the Upper Cretaceous Lopez de Bertodano Formation (late Campanian-Maastrichtian) of Seymour Island, Antarctic Peninsula include Cryptoclididae and Elasmosauridae. The occurrence of Cryptoclididae is reported from the Antarctic region for the first time. The taxon represents a new genus and species, based on a skull and associated cervical vertebrae. The long, slender and delicate teeth may have formed a ‘trapping’ device that enabled cryptoclidids to feed on small fish and crustaceans that abound in the same deposits. The cryptoclidids had a restricted distribution, being known so far from the Middle and Late Jurassic of England, and the Late Cretaceous of Chile, Argentina, and Antarctica. Other specimens, represented by several postcranial skeletons, are taxonomically indeterminate, but they share some features with other contemporary elasmosaurid genera such as Hydrotherosaurus, Morenosaurus, Thalassomedon , and Mauisaurus . Unlike the cryptoclidids, the elasmosaurids had a cosmopolitan distribution during the Jurassic and Cretaceous periods. Trophic diversity within guilds of marine predators is examined in the Lopez de Bertodano palaeocommunities. Three predator guilds are recognized on the basis of tooth morphology and prey preference. The mosasaurs composed the ‘Cut guild’, and were the principal predators. The elasmosaurids constituted the ‘Pierce guild’, and the cryptoclidids formed the ‘Trap guild’. These marine reptiles exploited the various pelagic resources such as sharks, bony fish, soft cephalopods and crustaceans, and survived until the end of the Cretaceous. The plesiosaurs were excellent swimmers, and used their hyperphalangic paddles for subaqueous flight in the manner of modern sea lions.
Enantiornithes is the most speciose clade of Cretaceous birds, but many taxa are known from isolated postcranial skeletons. Two embryonic enantiornithine bird skeletons of Gobipipus reshetovi gen. et sp. nov. from the Upper Cretaceous (Campanian) Barun Goyot Formation of the Gobi Desert in Mongolia provide new insights into the anatomy, radiation, and mode of development of early avialans. In recent times, both enantiornithine and ornithuromorph birds are known from the Barun Goyot Formation as well as from the Djadokhta and Nemegt Formations. The 80-million-year-old Gobipipus skeletons encased within eggshells shows several features characteristic of enantiornithine birds. The wing skeleton and shoulder girdle show morphological features indicating that Gobipipus achieved sophisticated powered flight. Gobipipus reshetovi gen. et sp. nov. is quite distinct from the sympatric enantiornithine species Gobipteryx minuta from the same strata in many anatomical features. Phylogenetic analysis of 26 avialan ingroup taxa based on distribution of 202 characters indicate that Gobipipus is a basal member of enantiornithine birds along with Confuciusornis and shares more characters with ornithuromorphs than previously recognized. The embryonic nature of Gobipipus specimens sheds new light on the developmental history of enantiornithine birds. The well-ossified bones of the fore- and hind limbs, and fusion of many skeletal elements indicate a precocial mode of development in Gobipipus. Apparently Gobipipus hatchlings could walk away from the ground nests as soon as they emerged from their eggs. The asymmetry of egg poles are unique features of Gobipipus eggs (oogenus Gobioolithus) among Cretaceous avialans. The microstructure of the shell in Gobioolithus eggs with the embryos of Gobipipus is typical avian (of ornithoid basic type) and less ratite-like in morphology of the spongy layer than is that in the other possible egg-remains of enantiornitine birds (oofamily Laevisoolithidae).