Theropods form a taxonomically and morphologically diverse group of dinosaurs that include extant birds. Inferred relationships between theropod clades are complex and have changed dramatically over the past thirty years with the emergence of cladistic techniques. Here, we present a brief historical perspective of theropod discoveries and classification, as well as an overview on the current systematics of non-avian theropods. The first scientifically recorded theropod remains dating back to the 17th and 18th centuries come from the Middle Jurassic of Oxfordshire and most likely belong to the megalosaurid Megalosaurus. The latter was the first theropod genus to be named in 1824, and subsequent theropod material found before 1850 can all be referred to megalosauroids. In the fifty years from 1856 to 1906, theropod remains were reported from all continents but Antarctica. The clade Theropoda was erected by Othniel Charles Marsh in 1881, and in its current usage corresponds to an intricate ladder-like organization of ‘family’ to ‘superfamily’ level clades. The earliest definitive theropods come from the Carnian of Argentina, and coelophysoids form the first significant theropod radiation from the Late Triassic to their extinction in the Early Jurassic. Most subsequent theropod clades such as ceratosaurs, allosauroids, tyrannosauroids, ornithomimosaurs, therizinosaurs, oviraptorosaurs, dromaeosaurids, and troodontids persisted until the end of the Cretaceous, though the megalosauroid clade did not extend into the Maastrichtian. Current debates are focused on the monophyly of deinonychosaurs, the position of dilophosaurids within coelophysoids, and megaraptorans among neovenatorids. Some recent analyses have suggested a placement of dilophosaurids outside Coelophysoidea, Megaraptora within Tyrannosauroidea, and a paraphyletic Deinonychosauria with troodontids placed more closely to avialans than dromaeosaurids.

Abstract Probabilistic fatigue models are required to account conveniently for several sources of uncertainty arising in the prediction procedures for structural details, such as the scatter in material behaviour. In this paper, a procedure to derive probabilistic S-N fields for structural details [1] is applied to a notched geometry with elliptic central hole made of puddle iron from the Eiffel bridge, based on the local approaches supported by the probabilistic ɛa–N or Smith–Watson–Topper (SWT)–N fields [1,2]. This procedure suggests an extension of the fatigue crack propagation model proposed by Noroozi et al. [3,4] to structural details, in order to cover both the fatigue crack initiation and fatigue crack propagation, based on local strain approaches to fatigue. Both fatigue crack initiation and fatigue crack propagation mechanisms are accounted for in the proposed approach. The numerical results are compared with available experimental S-N fatigue data for the notched plate under consideration.

In this work we calculate photoionization and X-ray production cross-sections (XPCS) of M-shell vacancies in Hg at incident photon energy of 5.96 keV (low.

In this article, we present a new technique to obtain estimators for parameters of ergodic processes. When a diffusion is ergodic its transition density converges to the invariant density Durett (1996). This convergence enabled us to introduce a sample partitioning technique that gives, in each subsample, observations that can be treated as independent and identically distributed. Within this framework, is possible the construction of estimators like maximum likelihood estimators or others.

In this session we review the Upper Cretaceous marine amniote records from the west coasts of North America and Africa. Recent work by our group in Angola, on the west coast of Africa, has opened up new fossiliferous localities, producing well-preserved turtles, plesiosaurs, and mosasaurs, ranging in age from Late Turonian to Late Maastrichtian. These African localities were deposited in arid latitudes and highly productive upwelling zones along the passive margin of a growing South Atlantic Ocean. The fossil record of Cretaceous marine amniotes from the West Coast of North America is relatively meager when compared to the African record and the prolific fossil beds laid down in the epicontinental seas of the Western Interior Seaway and northern Europe. Nonetheless, these localities provide an important glimpse of a marine ecosystem that developed on the active margins of a deep ocean basin. Historically considered to be depauperate and endemic, the west coast fauna was characterized by unusual forms such as Plotosaurus, arguably one of the most derived mosasaurs; however, in recent years, additional taxa have been described, revealing species diversity and ecological partitioning within these communities and in some cases, faunal interchange with other regions. The large quantity of well-preserved fossils from the west coast of Africa is influenced in part by its paleogeographic position, deposited within highly productive areas of Hadley Cell controlled upwelling zones. By contrast, the North American west coast localities have been deposited in temperate and higher latitudes since the Late Cretaceous. Nonetheless, the North American and African faunas share some common characteristics in a possessing a mix of endemic and more cosmopolitan forms. Habitat partitioning reflected in tooth form and body size is comparable between the Angolan and the North American west coast, and there is remarkable convergence in taxa which appear to exploit certain like-niches.