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 secular evolution of the Permian seawater 87 Sr/ 86 Sr ratios carries information about global tectonic processes, palaeoclimate and palaeoenvironments, such as occurred during the Early Permian deglaciation, the formation of Pangaea and the Permian–Triassic (P–Tr) mass extinction. Besides this application for discovering geological aspects of Earth history, the marine 87 Sr/ 86 Sr curve can also be used for robust correlations when other bio-, litho- and/or chemostratigraphic markers are inadequate. The accuracy of marine 87 Sr/ 86 Sr reconstructions, however, depends on high-quality age control of the reference data, and on sample preservation, both of which generally deteriorate with the age of the studied interval. The first-order Permian seawater 87 Sr/ 86 Sr trend shows a monotonous decline from approximately 0.7080 in the earliest Permian (Asselian) to approximately 0.7069 in the latest Guadalupian (Capitanian), followed by a steepening increase from the latest Guadalupian towards the P–Tr boundary ( c. 0.7071–0.7072) and into the Early Triassic. Various higher-order changes in slope of the Permian 87 Sr/ 86 Sr curve are indicated, but cannot currently be verified owing to a lack of sample coverage and significant disagreement of published 87 Sr/ 86 Sr records. Supplementary material: Numbers, information, data and references of the samples discussed are available at https://doi.org/10.6084/m9.figshare.c.3589460

Abstract: Permian rugose corals underwent evolutionary episodes of assemblage changeover, biogeographical separation and extinction, which are closely related to geological events during this time. Two coral realms were recognized, the Tethyan Realm and the Cordilleran–Arctic–Uralian Realm. These are characterized by the families Kepingophyllidae and Waagenophyllidae during the Cisuralian, Waagenophyllidae in the Guadalupian and the subfamily Waagenophyllinae in the Lopingian, and the families Durhaminidae and Kleopatrinidae during the Cisuralian and major disappearance of colonial and dissepimented solitary rugose corals from the Guadalupian to the Lopingian, respectively. The development of these coral realms is controlled by the geographical barrier resulting from the Pangaea formation. According to the changes in the composition and diversity of the Permian rugose corals, a changeover event might have occurred at the end-Sakmarian and is characterized by the mixed Pennsylvanian and Permian faunas to typical Permian faunas, probably related to a global regression. In addition, three extinction events are present at the end-Kungurian, the end-Guadalupian and the end-Permian, which are respectively triggered by the northward movement of Pangaea, the Emeishan volcanic eruptions and subsequent global regression, and the global climate warming induced by the Siberian Traps eruption.

Abstract: A brief historical review of ammonoid-based Permian biostratigraphy is performed. Changes in ammonoid associations are shown for each of nine Permian stages. The major correlation problems were discussed. A renewed ammonoid zonal scale is proposed.

Abstract: Establishing a Permian brachiopod biochronological scheme for global correlation is difficult because of strong provincialism during the Permian. In this paper, a brief overview of brachiopod successions in five major palaeobiogeographical realms/zones is provided. For Gondwanaland and peri-Gondwanan regions including Cimmerian blocks, Bandoproductus and Punctocyrtella (or Cyrtella ) are characteristic of the lower Cisuralian, as is Cimmeriella for the middle Cisuralian. As the Cimmerian blocks continued drifting north during the late Kungurian, accompanied by climate amelioration, contemporaneous brachiopods inhabiting these blocks showed a distinct shift from cold-water to mixed or warm-water affinities. However, coeval brachiopods in the Northern Transitional Zone (NTZ) are characterized by warm-water faunas and are associated with fusulinids in the lower Cisuralian. The Guadalupian brachiopods of the NTZ were clearly mixed between the Boreal and palaeoequatorial affinities. The end-Guadalupian is marked by the disappearance of a few characteristic genera, such as Vediproductus , Neoplicatifera and Urushtenoidea , in the Palaeotethyan region. The onset of the end-Permian mass extinction in the latest Changhsingian is clearly exhibited by the occurrence of the dwarfed and thin-shelled brachiopods commonly containing Paracrurithyris .