Two-billion-year-old evaporites capture Earth's great oxidation

Funding sources: Simons Foundation (SCOL 339006 to C.L.B.), European Research Council (ERC Horizon 2020 grant 678812 to M.C.), Research Council of Norway (RCN Centres of Excellence funding scheme project 223259 to K.P. and A.L.), Estonian Science Agency (PUT696 to K.K., A.L., K.P., T.K.).Major changes in atmospheric and ocean chemistry occurred in the Paleoproterozoic Era (2.5–1.6 billion years ago). Increasing oxidation dramatically changed Earth’s surface, but few quantitative constraints exist on this important transition. This study describes the sedimentology, mineralogy, and geochemistry of a remarkably preserved two-billion-year-old and ~800 meter-thick evaporite succession from the Onega Basin in Russian Karelia. The deposit consists of a basal unit dominated by halite (~100 m) followed by anhydrite-magnesite (~500 m) and dolomite-magnesite (~200 m) dominated units. The evaporite minerals robustly constraint marine sulfate concentrations to at least 10 millimoles per kilogram of water, representing an oxidant reservoir equivalent to over 20% of the modern ocean-atmosphere oxidizing capacity. These results show that substantial amounts of surface oxidant accumulated during this critical transition in Earth’s oxygenation.PostprintPeer reviewe

Identifying global vs. basinal controls on Paleoproterozoic organic carbon and sulfur isotope records

Paleoproterozoic sedimentary successions are important archives of the redox evolution of Earth's atmosphere and oceans. Efforts to unravel the dynamics of our planet's early oxygenation from this archive rely on various geochemical proxies, including stable carbon and sulfur isotopes. However, ancient metasedimentary rocks often experienced early- and late-stage (bio)geochemical processes making it difficult to discern primary environmental signals from bulk-rock δ13Corg and δ34S values. Such complexity in carbon and sulfur isotope systematics contributes to uncertainty about the redox structure of Paleoproterozoic oceans. A currently popular idea is that, following the Great Oxidation Event, global changes led to low-oxygen environments and temporally fluctuating ocean redox conditions that lasted until the Neoproterozoic. The volcano-sedimentary rocks of the Onega Basin have figured prominently in this concept, particularly the exceptionally organic-rich rocks of the 1.98 Ga Zaonega Formation. However, a growing body of evidence shows that local depositional processes acted to form the δ13Corg and pyrite δ34S records of the Zaonega Formation, thus calling for careful assessment of the global significance of these isotope records. Placing new and existing organic carbon and sulfur isotope data from the Zaonega Formation into the context of basin history and by comparing those results with key Paleoproterozoic successions of the Francevillian Basin (Gabon), the Pechenga Greenstone Belt (NW Russia) and the Animikie Basin (Canada), we show that the stratigraphic δ13Corg and pyrite δ34S trends can be explained by local perturbations in biogeochemical carbon and sulfur cycling without requiring global drivers. Despite their temporal disparity, we also demonstrate that individual successions share certain geological traits (e.g. magmatic and/or tectonic activity, hydrocarbon generation, basin restriction) suggesting that their pyrite δ34S and δ13Corg trends were governed by common underlying mechanisms (e.g. similar basinal evolution and biogeochemical feedbacks) and are not necessarily unique to certain time intervals. We further show that pyrites in these successions that are most likely to capture ambient seawater sulfate isotopic composition have consistent δ34S values of 15–18‰, which hints at remarkable stability in the marine sulfur cycle over most of the Paleoproterozoic Era.</p

Two-billion-year-old evaporites capture Earth’s great oxidation

Major changes in atmospheric and ocean chemistry occurred in the Paleoproterozoic Era (2.5–1.6 billion years ago). Increasing oxidation dramatically changed Earth’s surface, but few quantitative constraints exist on this important transition. This study describes the sedimentology, mineralogy, and geochemistry of a two-billion-year-old and ~800 m-thick evaporite succession from the Onega Basin in Russian Karelia. The deposit consists of a basal unit dominated by halite (~100 m) followed by anhydrite-magnesite (~500 m) and dolomite-magnesite (~200 m) dominated units. The evaporite minerals provide a robust constraint that marine sulfate concentrations were at least 10 mmol/kg, representing an oxidant reservoir equivalent to over 20% of the modern ocean-atmosphere oxidizing capacity. These results show that substantial amounts of surface oxidant accumulated during this critical transition in Earth’s oxygenation