Sedimentary Environment and Uranium Mineralization of the Neogene Shawan Formation in the Beisantai Uplift, Eastern Junggar Basin

IF 2.9 3区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Niannan Chen, Mangen Li*, Jianbing Duan*, Shengming Wu, Xiangfei Tang, PengFei Fan, Baowen Guan, Jin Wang and Rui Jin, 
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Abstract

The Beisantai Uplift, situated on the eastern margin of the Junggar Basin, has recently attracted attention due to the discovery of uranium-bearing strata within the Neogene Shawan Formation. This study investigates the depositional and diagenetic controls on uranium mineralization using back-scattered electron (BSE) microscopy, whole-rock geochemistry, and in situ trace element and sulfur isotope analyses of pyrite. Coffinite is the dominant uranium mineral, typically occurring along pyrite margins, within detrital fractures, and associated with calcite cement. Titanium–uranium oxides are distributed on rutile and pyrite surfaces or within calcite dissolution pores, indicating that uranium precipitation was governed by localized reducing microenvironments. Geochemical proxies such as Cr, V, Ni, Sr, and Ba suggest that the Shawan Formation was deposited under semisaline, arid conditions with high evaporation and weak oxidation─favoring early uranium mobility. Subsequently, δ34S values of pyrite (−48.08‰ to −40.26‰) indicate formation via bacterial sulfate reduction (BSR), with hydrocarbons providing both reducing agents (e.g., CH4, H2S) and sulfur sources. This hydrocarbon-driven BSR process led to early pyrite formation under strongly reducing the conditions. Uranium minerals are frequently observed replacing or surrounding pyrite, suggesting that pyrite acted as a redox buffer and facilitated U6+ reduction. The enrichment of redox-sensitive elements (Mo, U, Ni, Co) in ore-related pyrite further supports the development of sulfidic anoxic microenvironments. Collectively, mineralogical, isotopic, and geochemical evidence reveals a two-stage mineralization model: uranium was first introduced under oxidizing conditions and then locally precipitated in response to hydrocarbon-induced reducing environments. The close spatial and temporal association among hydrocarbons, pyrite, and uranium highlights their synergistic role in controlling mineralization within the Shawan Formation.

Abstract Image

准噶尔盆地东部北三台隆起新近系沙湾组沉积环境与铀成矿作用
北三台隆起位于准噶尔盆地东缘,新近系沙湾组含铀地层的发现引起了人们的广泛关注。本文利用背散射电子显微镜(BSE)、全岩地球化学、黄铁矿原位微量元素和硫同位素分析等方法研究了成矿作用的沉积成岩控制因素。Coffinite是主要的铀矿物,通常沿黄铁矿边缘,在碎屑裂缝中,并与方解石胶结伴生。钛铀氧化物分布在金红石和黄铁矿表面或方解石溶蚀孔内,表明铀沉淀受局部还原微环境控制。Cr、V、Ni、Sr、Ba等地球化学指标表明,沙湾组沉积条件为半盐碱、干旱、高蒸发、弱氧化条件,有利于早期铀的流动。随后,黄铁矿的δ34S值(- 48.08‰~ - 40.26‰)表明黄铁矿是由细菌硫酸盐还原(BSR)形成的,烃类同时提供还原剂(如CH4、H2S)和硫源。这种烃类驱动的BSR过程在强还原条件下形成了早期黄铁矿。铀矿物经常取代或包围黄铁矿,表明黄铁矿具有氧化还原缓冲作用,有利于U6+还原。与矿有关的黄铁矿中氧化还原敏感元素(Mo, U, Ni, Co)的富集进一步支持了硫化物缺氧微环境的发展。总的来说,矿物学、同位素和地球化学证据揭示了一个两阶段的成矿模式:铀首先在氧化条件下被引入,然后在烃类诱导的还原环境下局部沉淀。油气、黄铁矿、铀三者在时空上的密切联系凸显了它们在沙湾组成矿控制中的协同作用。
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来源期刊
ACS Earth and Space Chemistry
ACS Earth and Space Chemistry Earth and Planetary Sciences-Geochemistry and Petrology
CiteScore
5.30
自引率
11.80%
发文量
249
期刊介绍: The scope of ACS Earth and Space Chemistry includes the application of analytical, experimental and theoretical chemistry to investigate research questions relevant to the Earth and Space. The journal encompasses the highly interdisciplinary nature of research in this area, while emphasizing chemistry and chemical research tools as the unifying theme. The journal publishes broadly in the domains of high- and low-temperature geochemistry, atmospheric chemistry, marine chemistry, planetary chemistry, astrochemistry, and analytical geochemistry. ACS Earth and Space Chemistry publishes Articles, Letters, Reviews, and Features to provide flexible formats to readily communicate all aspects of research in these fields.
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