The redeposition of pristine phosphorite plays an important role in phosphorus accumulation, which created reworked phosphorite extensively on the continental shelf. This paper, using geochemical analysis combined with data from petrology and diagenesis, focuses on the reconstruction of the formation processes of the Late Cretaceous Thaniyat phosphorite deposition in northwestern Saudi Arabia, which is a part of the famous large Neo-Tethys Ocean’s phosphorite deposit. The results of our study illustrate that the phosphorites represent the reworked products from the north, close to the edge of the Neo-Tethys Ocean’s shelf, where upwelling had accreted the pristine phosphorite. The reworked phosphatic grains were redeposited near the shore in sandstone, forming sandy phosphorite and on a carbonate platform and creating calcareous phosphorite. The microscale sedimentological and geochemical information hosted in the eroded phosphorite grains indicates that the source sediment, pristine phosphorite, occurred under a fluctuating geophysical condition and in a relatively limited geochemical environment. They were physically crushed and transported landward and deposited under oxic conditions, forming the Thaniyat phosphorites. Early diagenesis in the Thaniyat phosphorite was evidenced by recrystallization of the phosphate minerals, geochemical depletion, and C and O isotope excursion.

The source of uranium is an important research topic related to the exploration of sandstone-type uranium deposits, and potential uranium sources in deep basins are often overlooked. Black organic-rich shale is a common uranium-bearing rock in deep sedimentary basins. However, relatively few studies have investigated the migration of uranium during hydrocarbon generation in and release from uranium-rich shale. In this study, the uranium-rich shale in the Chang 7 member of the Yanchang Formation of the Upper Triassic in the Ordos Basin was selected to investigate the migration of uranium and other trace elements during the thermal maturation of uranium-rich shale via a semiopen pyrolysis simulation system. The gas and liquid products as well as the solid residue were thoroughly analysed by means of multiple instruments. The results showed that uranium significantly migrated before hydrocarbon generation (Ro < 0.61%), with a leaching rate between 12.1% and 18.8%. The leaching rate of uranium during the hydrocarbon generation stage (0.63% < Ro < 1.35%) was relatively low, ranging from 0 to 7.2%. Cu, Pb, Zn, Mo, and other trace elements also migrated considerably during the early stage of thermal evolution, with leaching rates ranging from 2.9 ~ 11.6%. The yield of low-molecular-weight organic acids (LOAs) was the highest in the early stage of thermal maturity, and the LOA yield exhibited a good correlation with the leaching rates of Cu, Pb, Zn, Co, Mo, etc. The generation of LOAs from source rocks was conducive to the leaching and migration of trace elements. Moreover, according to a statistical analysis of published geochemical data, the total organic carbon (TOC) content, uranium content, and U/TOC ratio in shale decreased significantly with increasing burial depth, indicating that uranium migrated significantly upon kerogen hydrocarbon generation during thermal evolution. Therefore, uranium-rich shale is an important deep uranium source in sedimentary basins.