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all geography including DSDP/ODP Sites and Legs
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Vyatkian
UPPER PERMIAN VERTEBRATE COPROLITES FROM VYAZNIKI AND GOROKHOVETS, VYATKIAN REGIONAL STAGE, RUSSIAN PLATFORM
Disruption of playa–lacustrine depositional systems at the Permo-Triassic boundary: evidence from Vyazniki and Gorokhovets on the Russian Platform
Radioisotopic and biostratigraphic constraints on the classical Middle–Upper Permian succession and tetrapod fauna of the Moscow syneclise, Russia
Late Permian conchostracans (Crustacea, Branchiopoda) from continental deposits in the Moscow Syneclise, Russia
LAURUSSIAN-ASPECT OF THE COPROLITE ASSOCIATION FROM THE UPPER TRIASSIC (CARNIAN) OF THE ARGANA BASIN, MOROCCO
The age of North America’s youngest Paleozoic continental vertebrates: a review of data from the Middle Permian Pease River (Texas) and El Reno (Oklahoma) Groups
Abstract: The reverse polarity Kiaman Superchron has strong evidence for at least three, or probably four, normal magnetochrons during the early Permian. Normal magnetochrons are during the early Asselian (base CI1r.1n at 297.94±0.33 Ma), late Artinskian (CI2n at 281.24±2.3 Ma), mid-Kungurian (CI3n at 275.86±2.0 Ma) and Roa"dian (CI3r.an at 269.54±1.6 Ma). The mixed-polarity Illawarra Superchron begins in the early Wordian at 266.66±0.76 Ma. The Wordian–Capitanian interval is biased to normal polarity, but the basal Wuchiapingian begins the beginning of a significant reverse polarity magnetochron LP0r, with an overlying mixed-polarity interval through the later Lopingian. No significant magnetostratigraphic data gaps exist in the Permian geomagnetic polarity record. The early Cisuralian magnetochrons are calibrated to a succession of fusulinid zones, the later Cisuralian and Guadalupian to a conodont and fusulinid biostratigraphy, and Lopingian magnetochrons to conodont zonations. Age calibration of the magnetochrons is obtained through a Bayesian approach using 35 radiometric dates, and 95% confidence intervals on the ages and chron durations are obtained. The dating control points are most numerous in the Gzhelian–Asselian, Wordian and Changhsingian intervals. This significant advance should provide a framework for better correlation and dating of the marine and non-marine Permian.
Permian tetrapod biochronology, correlation and evolutionary events
Abstract: The most extensive Permian tetrapod (amphibian and reptile) fossil records from the western USA (New Mexico to Texas) and South Africa have been used to define 11 land vertebrate faunachrons (LVFs). These are, in ascending order, the Coyotean, Seymouran, Mitchellcreekian, Redtankian, Littlecrotonian, Kapteinskraalian, Gamkan, Hoedemakeran, Steilkransian, Platbergian and Lootsbergian. These faunachrons provide a biochronological framework with which to assign ages to, and correlate, Permian tetrapod fossil assemblages. Intercalated marine strata, radioisotopic ages and magnetostratigraphy were used to correlate the Permian LVFs to the standard global chronostratigraphic scale with varying degrees of precision. Such correlations identified the following significant events in Permian tetrapod evolution: a Coyotean chronofaunal event (end Coyotean); Redtankian events (Mitchellcreekian–Littlecrotonian); Olson’s gap (late Littlecrotonian); a therapsid event (Kapteinskraalian); a dinocephalian extinction event (end Gamkan); and a latest Permian extinction event (Platbergian–Lootsbergian boundary). Problems of incompleteness, endemism and taxonomy, and the relative lack of non-biochronological age control continue to hinder the refinement and correlation of a Permian timescale based on tetrapod biochronology. Nevertheless, the global Permian timescale based on tetrapod biochronology is a robust tool for both global and regional age assignment and correlation. Advances in Permian tetrapod biochronology will come from new fossil discoveries, more detailed biostratigraphy and additional alpha taxonomic studies based on sound evolutionary taxonomic principles.
Abstract: In 1841, Murchison coined the term Permian for strata in the Russian Urals. Recognition of the Permian outside of Russia and central Europe soon followed, but it took about a century for the Permian to be accepted globally as a distinct geological system. The work of the Subcommission on Permian Stratigraphy began in the 1970s and resulted in current recognition of nine Permian stages in three series: the Cisuralian (lower Permian) – Asselian, Sakmarian, Artinskian and Kungurian; the Guadalupian (middle Permian) – Roadian, Wordian and Capitanian; and the Lopingian (upper Permian) – Wuchiapingian and Changhsingian. The 1990s saw the rise of Permian conodont biostratigraphy, so that all Permian Global Stratigraphic Sections and Points (GSSPs) use conodont evolutionary events as the primary signal for correlation. Issues in the development of a Permian chronostratigraphic scale include those of stability and priority of nomenclature and concepts, disagreements over changing taxonomy, ammonoid v. fusulinid v. conodont biostratigraphy, differences in the perceived significance of biotic events for chronostratigraphic classification, and correlation problems between provinces. Further development of the Permian chronostratigraphic scale should focus on GSSP selection for the remaining, undefined stage bases, definition and characterization of substages, and further integration of the Permian chronostratigraphic scale with radioisotopic, magnetostratigraphic and chemostratigraphic tools for calibration and correlation.
Abstract The earliest history of Archosauriformes is mainly represented by members of Proterosuchidae and Erythrosuchidae, which are known worldwide from latest Permian to Middle Triassic beds. These two groups were historically combined within ‘Proterosuchia’, with approximately 30 nominal species. Two morphotypes have been recognized among proterosuchians: proterosuchids with a generally more sprawling gait and elongated and low skulls with an overhanging premaxilla, and the more heavily built erythrosuchids, with a probably less sprawling gait and large, presumably hypercarnivorous, skulls. The systematics of ‘Proterosuchia’ was relatively chaotic throughout most of the twentieth century, but currently there exists consensus regarding the non-monophyly of proterosuchians and their phylogenetic position outside all other archosauriforms. In contrast, the delimitation and taxonomic content of Proterosuchidae and Erythrosuchidae remain unstable. Few studies of proterosuchian palaeobiology have been carried out. Current lines of evidence favour a predominantly terrestrial lifestyle for proterosuchians. Limb bone histology indicates rapid continuous growth rates in Proterosuchus and Erythrosuchus before reaching sexual maturity. A better knowledge of proterosuchian anatomy, systematics, evolution and ecology is important for advancing understanding of the origin and early radiation of Archosauriformes and the patterns of biotic recovery following the Permo-Triassic mass extinction event. There remains much research to be carried out in proterosuchian palaeobiology.