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The Toarcian Oceanic Anoxic Event (T-OAE; ~183 Mya) was a globally significant carbon-cycle perturbation linked to widespread deposition of organic-rich sediments, massive volcanic CO2 release, marine faunal extinction, sea-level rise, a crisis in carbonate production related to ocean acidification, and elevated seawater temperatures. Despite recognition of the T-OAE as a potential analog for future ocean deoxygenation, current knowledge on the severity of global ocean anoxia is limited largely to studies of the trace element and isotopic composition of black shales, which are commonly affected by local processes. Here, we present the first carbonate-based uranium isotope (δ238U) record of the T-OAE from open marine platform limestones of the southeastern Tethys Ocean as a proxy for global seawater redox conditions. A significant negative δ238U excursion (~0.4‰) is recorded just prior to the onset of the negative carbon isotope excursion comprised within the T-OAE, followed by a long-lived recovery of δ238U values, thus confirming that the T-OAE represents a global expansion of marine anoxia. Using a Bayesian inverse isotopic mass balance model, we estimate that anoxic waters covered ~6 to 8% of the global seafloor during the peak of the T-OAE, which represents 28 to 38 times the extent of anoxia in the modern ocean. These data, combined with δ238U-based estimates of seafloor anoxic area for other CO2-driven Phanerozoic OAEs, suggest a common response of ocean anoxia to carbon release, thus improving prediction of future anthropogenically induced ocean deoxygenation. [ABSTRACT FROM AUTHOR]

Late Devonian marine systems were characterized by major environmental perturbations and associated biotic community changes linked to climate change and widespread oceanic anoxia. Here, we provide high-resolution lipid biomarker chemostratigraphic records from the Upper Devonian Chattanooga Shale (Tennessee, USA) to investigate algal-microbial community changes in the southern Illinois Basin that were related to contemporaneous shifts in marine redox (as proxied by trace metals, Fe-species, and Corg/P) and salinity conditions (as proxied by B/Ga, Sr/Ba, and S/total organic carbon). The Frasnian was characterized by dominantly bacterial lipids (high hopane/sterane), near-marine salinity, and a shift from oxic to increasingly reducing conditions in response to increasing organic carbon sinking fluxes. Aryl isoprenoids and aryl isoprenoid ratios reveal that the O2-H2S chemocline was unstable and intermittently shallow (i.e., within the photic zone). The Frasnian-Famennian boundary was marked by a shift in microalgal community composition toward green algal (e.g., prasinophyte) dominance (lower C27 and higher C28 and C29 steranes), a sharp reduction in watermass salinity, and a stable O2-H2S chemocline below the photic zone, conditions that persisted until nearly the end of the Famennian. We infer that changing watermass conditions, especially a sharp reduction in salinity to possibly low-brackish conditions (<10 psu), were the primary cause of concurrent changes in the microalgal community, reflecting tolerance of low-salinity conditions by green algae. Transient spikes in moretane/hopane (M/H) ratios may record enhanced terrestrial weathering at the Frasnian-Famennian and Devonian-Carboniferous boundaries, triggered by coeval glacioeustatic falls and increased inputs of soil organic matter. High M/H and pristane/phytane, in combination with low chemical index of alteration and K/Al, record a decrease in chemical weathering intensity during the Famennian that may have been due to contemporaneous climatic cooling, and a concurrent reduction in silt content may reflect stabilization of land surfaces by vascular plants and resulting reduced sediment yields. This study demonstrates the effectiveness of combining organic and inorganic geochemical proxies (including novel paleosalinity indices) for determination of environmental controls on the composition and productivity of plankton communities in paleomarine systems. [ABSTRACT FROM AUTHOR]

Late Cretaceous to Early Paleogene time represents a critical transitional period in Earth history. Global events include short-term instability in climate and ocean circulation, large igneous province emplacement, and catastrophic extinction of marine and terrestrial fauna due at least in part to a bolide impact event. The response of the ocean system to Cretaceous-Paleogene (K-Pg) global events has been the subject of much research, yet fundamental questions remain regarding carbon cycling, climate, ocean mixing, and redox conditions. To help elucidate paleoceanographic changes across the K-Pg transition, we revisit the classic Maastrichtian to Danian chalk-limestone succession at Stevns Klint, Denmark with a suite of new geochemical data, including insights from the redox-sensitive chromium isotope system. We use carbon and oxygen isotope trends to form a well-constrained framework for the succession, before presenting strontium isotope, chromium isotope, and rare-earth element data for the units deposited both before and after the K-Pg event. Carbon isotopes show only minor perturbation across the K-Pg boundary and oxygen isotopes record a prominent positive excursion, with both of these trends standing in contrast to many K-Pg boundary sections worldwide. Strontium isotopes record a spike towards more radiogenic values, which is consistent with a globally-observed, short-term weathering pulse. The chromium isotope profile of Maastrichtian chalk begins with strongly positive values followed by a sharp negative excursion associated with a facies shift and initiation of bottom currents in the Chalk Sea. δ 53 Cr values then recover, before falling steadily across the K-Pg boundary and into the Danian limestone. Chromium isotope trends do not correspond to changes in hydrothermal input or basin redox conditions—instead, we propose that mixing of water masses with distinct chromium isotope signatures controlled temporal chromium isotope variability. The local mixing event inferred from our Maastrichtian chromium isotope data could be related to a temporary inflow of Tethyan bottom waters, or the shift from end-Maastrichtian greenhouse warming (associated with Deccan volcanism) to the worldwide cooling phase that immediately preceded the K-Pg boundary. No immediate change in chromium isotopes is recorded across the K-Pg boundary, indicating that the bolide impactor did not substantially perturb the marine chromium cycle, at least at the scale resolvable by our data. Instead, chromium isotope trends continued to be controlled by local oceanographic processes, highlighting the potential of the chromium isotope system to record isotopic heterogeneity and mixing events in ancient oceans. [ABSTRACT FROM AUTHOR]

The article cites a research study that examines whether oceanic anoxia played a role in the decline of the Ediacara biota during the terminal Ediacaran Period. Uranium isotope compositions were measured from the Dengying Formation of South China to extract new constraints on the extent of global redox change during the period.