Pore systems in the Middle Permian Phosphoria Rock Complex (PRC), Rocky Mountain Region, USA, evolved with biotic and chemical dynamics in a shallow epicontinental seaway undergoing extreme environmental shifts. Biochemical responses to environmental changes directly affected pore systems and controlled diagenetic pathways through burial. Petrographic methods and spatially resolved measurements of δ 18 O in sequence stratigraphic context allow characterization of pore systems and their evolution in heterogenous biochemical sediments. Pore systems vary regionally and across systems tracts on second-order (9–10 million years [MY]) and third-order (2–5 MY) timescales. Minimal porosity occurs in transgressive mudrocks rich in organic matter (OM), phosphorites, and carbonates. Cool, acidic, low-oxygen, nutrient-rich basinal waters interacted with warm open to restricted shelfal waters in transgressions. This resulted in accumulation and microbial decay of S-rich OM, phosphatization, carbonate precipitation, silicification, as well as deposition of calcitic-biotic debris (bryozoans, brachiopods, and crinoids) and micrite. Relative to landward and highstand marine components, transgressive basinal marine carbonates and silica are δ 18 O depleted due to microbial decay of OM. Extensive cementation coupled with near-surface compaction and recrystallization of micrite occluded large portions of porosity in transgressive phosphorites and carbonates. Porosity in these rocks is dominated by interparticle and, to a lesser degree, intraparticle microporosity in microbored phosphatized and micritized grains. Phosphorites are compacted where cements are not pervasive. OM-rich sediments host minimal volumes of interparticle nanoporosity due to mechanical compaction and incursion of secondary OM (bitumen) during burial. PRC OM is S-rich, due to sulfate-reducing bacterial enrichment, and locally abundant. This drove early generation of secondary OM and inhibited OM-hosted porosity development through thermal maturation. Large volumes of porosity accumulated in highstand sediments and varied with transitions from silicisponge spicule cherts and calcitic-biota carbonates to pervasively dolomitized micritic, peloidal, aragonitic mollusk, and peritidal microbial sediments. These biochemical transitions, and ultimately pore-system evolution, were driven by interaction between oxygenated open marine waters, eolian siliciclastic debris, and increasingly restricted shelfal waters. Marine carbonate and silica δ 18 O are consistent with Middle Permian open marine waters but are enriched landward and through highstands with evaporative fractionation. This δ 18 O-enriched authigenic silica in carbonates and evaporite replacements, as well as δ 18 O enrichment through silica precipitation, suggest dolomitization and silicification were driven by evaporitic processes. In spiculitic cherts and siltstones, silicification and carbonate diagenesis resulted in small volumes of intraparticle, interparticle, and moldic porosity, as well as increased susceptibility to fracturing and associated permeability enhancement. Chalcedony in spiculites and silicified carbonates host minor volumes of porosity where moganite crystallites dissolved during hydrocarbon migration. Highstand dolomites host abundant intercrystalline, moldic, fenestral, and interparticle macroporosity and microporosity, especially in peloidal wackestones, mollusk debris, ooid grainstones, and peritidal microbialites. Dolomitization resulted in dissolution of aragonitic mollusk and ooids, cementation, and preservation of primary porosity. Porosity loss through burial in dolomites occurs through mechanical compaction, and to a lesser degree, precipitation of zoned carbonate cements that are δ 18 O depleted relative to earlier dolomite. Compaction strongly decreases intercrystalline porosity in dolomitized peloidal wackestones. Secondary OM related to hydrocarbon migration coats surfaces and fills small pore volumes, inhibiting burial cementation.

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 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.

Abstract: Forty Permian conodont biozones are summarized and 35 additional regional zones are correlated. The Lower Permian is largely zoned on the basis of partial range lineage interval zones of species of Streptognathodus , Sweetognathus , Neostreptognathodus and Mesogondolella . The Middle and Upper Permian are zoned, respectively, on the basis of partial range lineage interval zones of species of Jinogondolella and Clarkina . The ranges of all key taxa to develop this zonation are depicted in relation to the geochronological ages of Permian stages. The lowest Permian succession has been astronomically tuned with 400 kyr cyclothems linked to interpolated ages in the Uralian succession.

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 .