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The geochemistry of phosphate rocks can provide valuable information on their depositional environment and the redox condition of global oceans through time. Here we examine trace metal concentrations and uranium (δ238U, δ234U) and strontium (87Sr/86Sr) isotope variations of marine sedimentary phosphate rocks and the phosphate-bearing carbonate fluorapatite (CFA) mineral phase, originating from Precambrian to mid-Miocene aged major global phosphate deposits. We find elevated concentrations of several trace elements (Al, V, Cr, Cd, U, Mn, Co, Cu, As, and Rb) in the CFA mineral phase of young phosphate rocks (Miocene to Late Cretaceous) relative to those of older (Devonian to Precambrian) rocks. The δ238U of phosphate rocks of Mid-Miocene to Permian age range from −0.311‰ to 0.070‰, exhibiting a positive fractionation relative to modern seawater (−0.38‰). This is similar to the isotope fractionation reported for carbonate and shale sediments, likely resulting from the reduction of uranium in porewaters during CFA precipitation. Cambrian to Precambrian phosphate rocks have lower δ238U of −0.583‰ to −0.363‰, indicating different depositional redox conditions likely resulting from seafloor anoxia and/or diagenetic modification. The 87Sr/86Sr ratios of phosphate rocks of Cretaceous to Mid-Miocene age generally follow the secular 87Sr/86Sr seawater curve. Phosphate rocks with 87Sr/86Sr that deviate from this curve have characteristic trace metal trends, such as lower Sr/Ca and Sr concentrations, suggesting later diagenetic modification. Older phosphate rocks of Precambrian age are systematically more radiogenic than the expected secular Sr seawater composition at the time of deposition, possibly due to the greater influence of terrestrial input in peritidal zones and/or more pervasive diagenetic modification. Overall, our study reveals connections between U and Sr isotope variations for reconstructing the depositional and diagenetic conditions of global phosphate rock formation through Earth history and the transition to an oxic ocean following the Paleozoic Oxygenation Event. 

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 CO₂release, 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.