The fossil record for neoceratopsian (horned) dinosaurs in the Lower Cretaceous of North America primarily comprises isolated teeth and postcrania of limited taxonomic resolution, hampering previous efforts to reconstruct the early evolution of this group in North America. An associated cranium and lower jaw from the Cloverly Formation (?middle-late Albian, between 104 and 109 million years old...

The flowering plants that dominate modern vegetation possess leaf gas exchange potentials that far exceed those of all other living or extinct plants. The great divide in maximal ability to exchange CO(2) for water between leaves of nonangiosperms and angiosperms forms the mechanistic foundation for speculation about how angiosperms drove sweeping ecological and biogeochemical change during the...

The Late Cretaceous was a time of tremendous global change, as the final stages of the Age of Dinosaurs were shaped by climate and sea level fluctuations and witness to marked paleogeographic and faunal changes, before the end-Cretaceous bolide impact. The terrestrial fossil record of Late Cretaceous Europe is becoming increasingly better understood, based largely on intensive fieldwork over th...

A short review of the state of the art of research on insects from the Cretaceous period is given. The recent achievements and priorities for future efforts are indicated. © 2014 Elsevier Ltd. All rights reserved. The Cretaceous, the geologic period from circa 145 to 66 million years (Ma) ago is a complex time period in Earth's history (Gale, 2000; Keller, 2008; Cohen et al., 2013). Generally s...

The Peirópolis paleontological site (Late Cretaceous, Maastrichtian) in Minas Gerais State, Brazil yielded an important assemblage of fossil vertebrates. The typical occurrence of South American widespread taxa in Peirópolis is important for correlation between the Brazilian Bauru Basin and Argentinean Late Cretaceous basins. The fishes, turtles, anuran, crocodilians and dinosaurs known from Pe...

Testing models of macroevolution, and especially the sufficiency of microevolutionary processes, requires good collaboration between molecular biologists and paleontologists. We report such a test for events around the Late Cretaceous by describing the earliest penguin fossils, analyzing complete mitochondrial genomes from an albatross, a petrel, and a loon, and describe the gradual decline of ...

Nuurcala obesa sp. n., in the cockroach family Caloblattinidae, is described from the Lower Cretaceous Yixian Formation (Liaoning Province, China) based on a combination of differential characters of fore- and hind wing venation, colouration and body structures. Systematically, Nuurcala (Vršanský, 2003), known from the Cretaceous sediments of Bon Tsagaan and Khurilt, Mongolia, is closely relate...

Myanmymar aresconoidesgen n., sp. n. is described from one female in Burmese amber, dated as about 100 my. It is similar to Arescon on wing features but is unique among Mymaridae in having distinctly segmented palpi. It is the fifth mymarid genus definitely referable to the Cretaceous period. A key to Cretaceous mymarid genera is presented and the features of Myanmymar are compared with the oth...

Rhynchocephalian lepidosaurs, though once widespread worldwide, are represented today only by the tuatara (Sphenodon) of New Zealand. After their apparent early Cretaceous extinction in Laurasia, they survived in southern continents. In South America, they are represented by different lineages of Late Cretaceous eupropalinal forms until their disappearance by the Cretaceous/Palaeogene (K/Pg) bo...

The late Middle Jurassic–early Eocene (;120 m.y.) sediment-accumulation history of the Cordilleran foreland basin in northern Utah exhibits a sigmoidal pattern on a rate vs. time plot, with moderate rates of accumulation during late Middle Jurassic, very low net rates during Late Jurassic–earliest Cretaceous, increasingly rapid rates during Earlymiddle Cretaceous, and low rates during Late Cret...