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Oil-source correlation studies have demonstrated that the crude oils in the Ordos Basin were mainly derived from organic-rich lacustrine mudstones of the Yanchang Formation. The sedimentology, petrology and organic geochemistry of these mudstones have been studied intensively, but their trace and rare earth element (REE) characteristics have received little attention. In this paper, we present trace and rare earth element data of the Upper Triassic Yanchang Formation mudstones in the southern Ordos Basin to constrain the palaeoenvironment, provenance and depositional setting. Our results show that the REE and trace element concentrations of the Yanchang Formation mudstones are higher than those of the upper continental crust (UCC). The Sr contents and Sr/Ba and Y/Ho ratios of these mudstones indicate the absence of a marine transgression during the sedimentation of the Upper Triassic mudstones. The depositional environment of the Upper Triassic mudstones was slightly oxic as evidenced by the values of Eu/Eu*, Ce/Ce*, Ce anom , δU, U/Th, V/Cr and Ni/Co. The UCC-normalized distribution pattern of REEs, spider diagrams, the ratios of related elements, the bivariate diagrams of Th/Sc-Zr/Sc and La/Th-Hf and the ternary plots of La-Th-Sc and Th-Sc-Zr/10 signify that the provenances of the Chang9-7 mudstones were mainly derived from a continental island arc, whereas the provenances of the Chang6-3 mudstones were mainly derived from a mixture of continental island arc and active continental margin, and the latter contain less recycled materials. Combined with the previous studies of detrital zircon dating and petrography of the Yanchang Formation sandstones in the southern Ordos basin, we propose that the Qinling orogenic belt served as one of the primary source regions occurring between the Chang7 and Chang6 periods, corresponding to the initial uplift of the west Qinling Mountains due to the collision between the Yangtze and North China blocks.

Removal of calcium and magnesium ions through biomineralization induced by bacteria has been proven to be an effective and environmentally friendly method to improve water quality, but the process and mechanism are far from fully understood. In this study, a newly isolated probiotic Bacillus licheniformis SRB2 (GenBank: KM884945.1) was used to induce the bio-precipitation of calcium and magnesium at various Mg/Ca molar ratios (0, 6, 8, 10, and 12) in medium with 30 g L−1 sodium chloride. Due to the increasing pH and HCO3− and CO32− concentrations caused by NH3 and carbonic anhydrase, about 98% Ca2+ and 50% Mg2+ were precipitated in 12 days. The pathways of bio-precipitation include extracellular and intracellular processes. Biominerals with more negative δ13C values (−16‰ to −18‰) were formed including calcite, vaterite, monohydrocalcite, and nesquehonite with preferred orientation. The nucleation on extracellular polymeric substances was controlled by the negatively charged amino acids and organic functional groups. The intracellular amorphous inclusions containing calcium and magnesium also contributed to the bio-precipitation. This study reveals the process and mechanism of microbial desalination for the removal of calcium and magnesium, and provides some references to explain the formation of the nesquehonite and other carbonate minerals in a natural and ancient earth surface environment.

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