Abstract A new locality for low-latitudinal, Early Triassic fishes was discovered in the Candelaria Hills, southwestern Nevada (USA). The fossils are derived from the lower Candelaria Formation, which was deposited during the middle–late Dienerian (late Induan), ca. 500 ka after the Permian-Triassic boundary mass extinction event. The articulated and disarticulated Osteichthyes (bony fishes), encompassing both Actinistia (coelacanths) and Actinopterygii (ray-fins), are preserved in large, silicified concretions that also contain rare coprolites. We describe the first actinopterygians from the Candelaria Hills. The specimens are referred to Pteronisculus nevadanus new species (Turseoidae?), Ardoreosomus occidentalis new genus new species (Ptycholepidae), the stem neopterygian Candelarialepis argentus new genus new species (Parasemionotidae), and Actinopterygii indet. representing additional taxa. Ardoreosomus n. gen. resembles other ptycholepids, but differs in its more angulate hyomandibula and lack of an elongate opercular process. Candelarialepis n. gen. is one of the largest parasemionotids, distinguished by its bipartite preopercle and scale ornamentation. Presented new species belong to genera ( Pteronisculus ) or families (Ptycholepidae, Parasemionotidae) that radiated globally after the mass extinction, thus underlining the striking similarities between Early Triassic (pre-Spathian) osteichthyan assemblages. The current data suggest that the diversity of low-latitudinal, Early Triassic bony fishes may have been greater than indicated thus far by the fossil record, probably due to sampling or taphonomic failure. All 24 fossils from the Candelaria Hills represent mid-sized or large osteichthyans, confirming the obvious absence of very small species (≤ 10 cm adult body length) in the beginning of the Mesozoic Era—even in low latitudes. UUID: http://zoobank.org/6a66ac96-d6b7-4617-94db-5a93cdb14215
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Abstract In the aftermath of the end‐ P ermian mass extinction, E arly T riassic sediments record some of the largest P hanerozoic carbon isotopic excursions. Among them, a global S mithian‐negative carbonate carbon isotope excursion has been identified, followed by an abrupt increase across the S mithian– S pathian boundary ( SSB ; ~250.8 Myr ago). This chemostratigraphic evolution is associated with palaeontological evidence that indicate a major collapse of terrestrial and marine ecosystems during the L ate S mithian. It is commonly assumed that S mithian and S pathian isotopic variations are intimately linked to major perturbations in the exogenic carbon reservoir. We present paired carbon isotopes measurements from the T haynes G roup ( U tah, USA ) to evaluate the extent to which the E arly T riassic isotopic perturbations reflect changes in the exogenic carbon cycle. The δ 13 C carb variations obtained here reproduce the known S mithian δ 13 C carb ‐negative excursion. However, the δ 13 C signal of the bulk organic matter is invariant across the SSB and variations in the δ 34 S signal of sedimentary sulphides are interpreted here to reflect the intensity of sediment remobilization. We argue that M iddle to L ate S mithian δ 13 C carb signal in the shallow marine environments of the T haynes G roup does not reflect secular evolution of the exogenic carbon cycle but rather physicochemical conditions at the sediment–water interface leading to authigenic carbonate formation during early diagenetic processes.
Abstract We describe here the early Spathian (Early Triassic) Paris Biota decapod fauna from the western USA basin. This fauna contains two taxa of Aegeridae (Dendobranchiata), namely Anisaeger longirostrus n. sp. and Aeger sp. that are the oldest known representatives of their family, thus extending its temporal range by 5 Myr back into the Early Triassic. This fauna also includes two representatives of Glypheida (Pleocyemata) with Litogaster turnbullensis and Pemphix krumenackeri n. sp., confirming for the former and extending for the latter the temporal ranges of their respective superfamilies back to the Early Triassic. Overall, the Paris Biota decapods are some of the oldest known representatives of Decapoda, filling in an important gap in the evolutionary history of this group, especially during the Triassic that marks the early diversification of this clade. Additionally, we compile and provide overviews for all known Triassic decapods, which leads to the revision of four species of Middle and Late Triassic Aegeridae, and to a revised family assignment of a Middle Triassic Glypheida. Based on this refined dataset, we also investigate decapod diversity throughout the Triassic. We show that the apparent increase in decapod taxonomic richness is probably driven by the heterogeneity of the fossil record and/or sampling effort, and that the decapod alpha diversity is actually relatively high as soon as the Early Triassic and remains rather stable throughout the Triassic. UUID: http://zoobank.org/0f435f27-1767-473d-955c-57fe869faa0f
Abstract 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.
Abstract In Timpoweap Canyon near Hurricane (Utah, USA), spectacular outcrop conditions of Early Triassic rocks document the geometric relationships between a massive Smithian fenestral-microbial unit and underlying, lateral and overlying sedimentary units. This allows us to reconstruct the evolution of depositional environments and high-frequency relative sea-level fluctuations in the studied area. Depositional environments evolved from a coastal plain with continental deposits to peritidal settings with fenestral-microbial limestones, which are overlain by intertidal to shallow subtidal marine bioclastic limestones. This transgressive trend of a large-scale depositional sequence marks a long-term sea-level rise that is identified worldwide after the Permian–Triassic boundary. The fenestral-microbial sediments were deposited at the transition between continental settings (with terrigenous deposits) and shallow subtidal marine environments (with bioturbated and bioclastic limestones). Such a lateral zonation questions the interpretation of microbial deposits as anachronistic and disaster facies in the western USA basin. The depositional setting may have triggered the distribution of microbial deposits and contemporaneous marine biota. The fenestral-microbial unit is truncated by an erosional surface reflecting a drop in relative sea level at the scale of a medium depositional sequence. The local inherited topography allowed the recording of small-scale sequences characterized by clinoforms and short-distance lateral facies changes. Stratal stacking pattern and surface geometries allow the reconstruction of relative sea-level fluctuations and tracking of shoreline migrations. The stacking pattern of these small-scale sequences and the amplitude of corresponding high-frequency sea-level fluctuations are consistent with climatic control. Large- and medium-scale sequences suggest a regional tectonic control.
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