Reconstructing the depositional environment and diagenetic modification of global phosphate deposits through integration of uranium and strontium isotopes

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.