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Evaporites are widely distributed within continental "red beds" in the Lanping–Simao Basin, west Yunnan, China. Sr (Strontium), S (Sulfur), and O (Oxygen) isotope compositions have been measured on 54 sulfate or/and sulfate-bearing samples collected from Lanping, Nuodeng, Jinggu, Mengyejing, Baozang throughout the Lanping–Simao Basin. The 87Sr/86Sr ratios of all samples (0.708081 to 0.710049) are higher than those of contemporaneous seawater, indicating a significant continental contribution to the drainage basin. Sulfates in the Lanping Basin have higher 87Sr/86Sr ratios (0.709406 to 0.710049) than those (0.708081 to 0.709548) in the Simao Basin. Nevertheless, the δ34S values of gypsums (13.4‰ to 17.6‰) in Lanping and Baozang fall within the range of Cretaceous seawater. Gypsums from a single section in Baozang have trends of decreasing δ34S values and increasing 87Sr/86Sr ratios from base to top, indicating continental input played an increasingly significant role with the evaporation of brines. High δ34S values (20.5‰ to 20.7‰) of celestites in Lanping are probably caused by bacterial sulfate reduction (BSR) process in which 34S were enriched in residual sulfates and/or recycling of Triassic evaporites. The reduced δ34S values of gypsums (9.5‰ to 10.4‰) in Nuodeng could have been caused by oxidation of sulfides weathered from Jinding Pb-Zn deposit. The complex O isotope compositions indicate that sulfates in the Lanping–Simao Basin had undergone sulfate reduction, re-oxidation, reservoir effects, etc. In conclusion, the formation of continental evaporites was likely derived from seawater due to marine transgression during the Cretaceous period. Meanwhile, non-marine inflows have contributed to the basin significantly. [ABSTRACT FROM AUTHOR]

The Mengyejing potash deposit is located in the southern port of the Simao Basin, Yunnan Province, and is hosted in mid-Cretaceous strata. The chemical compositions of fluid inclusions in halite crystals, collected from the level-610 adit in the deposit, were analysed by laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS). The results show that the brine is of the Na-K-Mg-Ca-Cl type and has K concentrations that are distinctly higher than those of Mg and Ca, unlike normal brines associated with Cretaceous halite. The high K concentrations indicate that the degree of evaporation of the ancient Mengyejing saline lake was very high, reaching the sylvite deposition stage but rarely reaching the carnallite deposition stage. The trajectory of the H and O isotopic compositions of the brines in the halite-hosted fluid inclusions corresponds to intense evaporation, indicating that the net evaporation exceeded the net inflow of brines. These brine compositions in halite-hosted fluid inclusions were likely formed by the dissolution of previously deposited K-bearing minerals by fresh continental and/or seawater, forming a type of modified seawater, with deep hydrothermal fluids potentially supplying additional potassium. The basin likely experienced multiple seawater incursion, dissolution and redeposition events in a high-temperature environment with high evaporation rates. [ABSTRACT FROM AUTHOR]

Two types of potash ores were sampled from the Mengyejing potash deposit (the MPD) which is the only ancient potash deposit ever found in China. Geochemical analyses, including Br, K, Mg and some heavy metals, were performed on those samples. The relatively consistent Br contents (141.42 to 763.67 ppm) in both bedded potash and veined potash ores show that the potash-forming brine was likely derived from seawater. K contents and Br/Cl ratios of the veined potash ores are relatively high in contrast to bedded potash ores. The K/Br ratios of veined potash ores exhibit a positive correlation with Br contents, which is opposite to that of the bedded potash ore of the MPD and potassium-salts from the evaporation of modern seawater. The contents of heavy metals in veined potash ores are much higher than those of bedded potash ores in the MPD and potash in other evaporite basins of the world. Sr and S isotopic compositions of these two types of potash ores suggest that the brines for precipitating veined potash were formed by mixing of connate waters (seawater or/and continental freshwater) and hydrothermal fluids. The geochemical and petrological characteristics of the veined potash ores indicate that the brine for forming veined potash orebodies caused by dissolution of previous bedded potash orebodies by hydrothermal fluids. The veined potash orebodies were formed through a cooling process by which sylvite precipitated first prior to halite. [ABSTRACT FROM AUTHOR]