The Neoproterozoic Era witnessed two low-latitude glaciations, which exerted a fundamental influence on ocean-atmosphere redox conditions and biogeochemical cycling. Climate models and palaeobiological evidence support the belief that open waters provided oases for life that survived snowball Earth glaciations, yet independent geochemical evidence for marine redox conditions during the Marinoan glaciation remains scarce owing to the apparent lack of primary marine precipitates. In this study, we explore variability in rare earth elements (REEs) and trace metal concentrations in dolostone samples of the Cryogenian Nantuo Formation taken from a drill core in South China. Petrological evidence suggests that the dolostone in the Nantuo Formation was formed in near-shore waters. All the examined dolostone samples featured significant enrichment of manganese (345-10,890 ppm, average 3488 ppm) and middle rare earth elements (MREEs) (Bell Shape Index: 1.43-2.16, average 1.76) after being normalized to Post-Archean Australian Shale (PAAS). Most dolostone samples showed slight to no negative Ce anomalies (Ce*/Ce 0.53-1.30, average 0.95), as well as positive Eu anomalies (Eu*/Eu 1.77-3.28, average 1.95). This finding suggests that the dolostone samples were deposited from suboxic to iron-enriched and anoxic waters. Although total REE concentrations correlated positively with Th concentrations in dolostone samples, MREE-enriched PAAS-normalized patterns preclude the conclusion that REEs were largely introduced by terrestrial contamination. Rather, we interpret the correlation between REEs and Th as an indication that the former were transported by colloids and nanoparticles in meltwaters. Taken together, we propose that anoxic and ferruginous water columns dominated in South China during the Marinoan glaciation with a thin oxic/suboxic layer restricted to coastal waters. The extreme anoxic and ferruginous conditions prevailing in the Cryogenian would have provided a baseline for subsequent transient Ediacaran ocean oxygenation and life evolution.

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The generation of acid mine drainage (AMD) may accelerate watershed erosion and promote the migration of heavy metals, then threaten local ecosystems such as aquatic life and even human health. Previous studies have focused primarily on influence of AMD in surface environment. In order to reveal the acidizing processes in karst high-sulfur coalfield in Southwest China, this study, by contrast, focused on the hydrogeochemical evolution process and acidification mechanism of mine water in Zhijin coalfield, western Guizhou Province. The oxidation of pyrite and other sulfides induced strong acidification of mine water according to the water chemical analysis. As a result, a series of geochemical processes such as dissolution of carbonates and silicates, hydrolysis of metal ions, and degassing of CO complicated water chemical evolution. The dissolution of silicates controlled the chemical composition of mine water, but more carbonates might be dissolved during the acidification of mine water. The sources of sulfate are quite different in water samples collected from the two selected mine. According to sulfur isotope analysis, the dissolution of gypsum is the primary source of sulfate in samples from Hongfa mine, whereas sulfide oxidation contributed a large amount of sulfate to the mine water in Fenghuangshan mine. The dissolution of carbonates should be an important source of DIC in mine water and CO originating from organic mineralization might also have a certain contribution. This study elucidated the groundwater chemical evolution processes in high-sulfur coal-bearing strata and provided a foundation for further study of carbonates erosion and carbon emission during acidification of mine water.

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