Smithian Strata and Non-Smithian Strata

The International Stratigraphic Guide defined that all stratified or quasi-stratified rock bodies of the earth crust, including sedimentary, igneous, metamorphic, solidified and unsolidified ones, should be considered as research contents of stratigraphy. Traditional stratigraphy mainly involves strata formed under gravity mechanism, plus a few kinds of bedded volcanic rocks such as lava, pyroclastic rock and volcanic ash, as well as metamorphic sedimentary and volcano-sedimentary rocks. These traditional strata are regarded as Smithian strata in this paper. In modem stratigraphy, mechanism of strata formation includes not only gravity but also thermal (ophiolite), mechanic and tectonic forces (orogenic melange and tectonite). In these above-mentioned non-gravitative conditions, the strata,formed complying with their own mechanisms but not with the law of superposition of Smithian stratigraphy, are called non-Smithian strata here. In melange regions from orogenic belt, formations of nonSmithian strata could be classified into subduct-scrape-match, subduct-retm-n-match, and subduct-overthrnst twits.     

Microbial deposits in the aftermath of the end‐Permian mass extinction: A diverging case from the Mineral Mountains (Utah,USA)

The Lower Triassic Mineral Mountains area (Utah, USA) preserves diversified Smithian and Spathian reefs and bioaccumulations that contain fenestral‐microbialites and various benthic and pelagic organisms. Ecological and environmental changes during the Early Triassic are commonly assumed to be associated with numerous perturbations (productivity changes, acidifica‐tion, redox changes, hypercapnia, eustatism and temperature changes) post‐dating the Permian–Triassic mass extinction. New data acquired in the Mineral Mountains sediments provide evidence to decipher the relationships between depositional environments and the growth and distribution of microbial structures. These data also help to understand better the controlling factors acting upon sedimentation and community turnovers through the Smithian–early Spathian. The studied section records a large‐scale depositional sequence during the Dienerian(?)–Spathian interval. During the transgression, depositional environments evolved from a coastal bay with continental deposits to intertidal fenestral–microbial limestones, shallow subtidal marine sponge–microbial reefs to deep subtidal mud‐dominated limestones. Storm‐induced deposits, microbialite–sponge reefs and shallow subtidal deposits indicate the regression. Three microbialite associations occur in ascending order: (i) a red beds microbialite association deposited in low‐energy hypersaline supratidal conditions where microbialites consist of microbial mats and poorly preserved microbially induced sedimentary structure; (ii) a Smithian microbialite association formed in moderate to high‐energy, tidal conditions where microbialites include stromatolites and associated carbonate grains (oncoids, ooids and peloids); and (iii) a Spathian microbialite association developed in low‐energy offshore conditions that is preserved as multiple decimetre thick isolated domes and coalescent domes. Data indicate that the morphologies of the three microbialite associations are controlled primarily by accommodation, hydrodynamics, bathymetry and grain supply. This study suggests that microbial constructions are controlled by changes between trapping and binding versus precipitation processes in variable hydrodynamic conditions. Due to the presence of numerous metazoans associated with microbialites throughout the Smithian increase in accommodation and Spathian decrease in accommodation, the commonly assumed anachronistic character of the Early Triassic microbialites and the traditional view of prolonged deleterious conditions during the Early Triassic time interval is questioned.     

Evolution of depositional settings in the Torrey area during the Smithian (Early Triassic,Utah, USA) and their significance for the biotic recovery

This work focuses on well‐exposed Lower Triassic sedimentary rocks in the area of Torrey (south‐central Utah, USA). The studied Smithian 8 deposits record a large‐scale third‐order sea‐level cycle, which permits a detailed reconstruction of the evolution of depositional settings. During the middle Smithian, peritidal microbial limestones associated with a rather low‐diversity benthic fauna were deposited seaward of the tidal flat siliciclastic red beds. Associated with siliceous sponges, microbial limestones formed small m‐scale patch reefs. During the late middle to late Smithian interval, the sedimentary system is characterized by tidal flat dolostones of an interior platform, ooid‐bioclastic deposits of a tide‐dominated shoal complex, and mid‐shelf bioclastic limestones. Microbial deposits, corresponding to sparse stromatolites formed in the interior platform, are contemporaneous with a well‐diversified marine fauna living in a seaward shoal complex and mid‐shelf area. The nature and distribution of these Smithian microbial deposits are not related to any particular deleterious environmental condition, highlighting that observed patterns of biotic recovery after the end‐Permian mass extinction were directly influenced by depositional settings. Facies evolution and stratal stacking patterns allow us to identify large, medium and small‐scale, as well as elementary depositional sequences. Large‐ and medium‐scale sequences are consistent with sea‐level changes, whereas small‐scale and elementary sequences are better explained by autocyclic processes. Copyright © 2015 John Wiley & Sons, Ltd.