印度Chilpi盆地黄铁矿的粒度δ34S分带:元古代封闭系统微生物硫酸盐还原的证据

IF 3.6 2区 地球科学 Q1 GEOCHEMISTRY & GEOPHYSICS
Susobhan Neogi, Trisrota Chaudhuri
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引用次数: 0

摘要

本研究首次记录了印度中部巴斯塔克拉通的元古代火山-沉积序列——Chilpi盆地的叠层石碳酸盐岩。该序列由浅层碎屑沉积向化学沉积过渡,泥晶灰岩与同沉积重晶石和寄主穹状叠层石互层,上覆千层岩。分布在这些微生物岩中的自面体成岩黄铁矿,保存了动态浅海环境中微生物和地球化学过程的高分辨率档案。采用大几何次离子质谱(SIMS)对黄铁矿颗粒进行了107个原位硫同位素(34S/32S)分析;CAMECA IMS-1300 HR3)的δ34SV-CDT值为+22.9‰~ +33.5‰。较大的颗粒表现出明显的晶内分带,相对于较轻的岩心(+25.5‰~ +33.5‰),晶缘富集34s,与半封闭成岩条件下微生物硫酸盐还原(MSR)的瑞利蒸馏相一致。较小的颗粒表现出最小的内部变化,反映了局部氧化还原微环境中颗粒的特定历史。瑞利模型表明,在黄铁矿生长过程中,原始硫酸盐储层损耗约41%。岩石学和BSE成像显示了方解石-石英过度生长和磁铁矿边缘等特征,支持黄铁矿的两阶段成岩生长,随后是部分氧化和磁铁矿取代。叠层石纹层中的层状重晶石记录了在氧气到亚氧气条件下钡和硫酸盐可用性的脉冲,可能与间歇性的火山或热液输入有关,而随后的黄铁矿和磁铁矿记录了从还原到再氧化条件的进展。这个矿物学序列——从重晶石到黄铁矿再到磁铁矿——在颗粒尺度上捕获了一个完整的氧化还原循环。因此,Chilpi盆地提供了一个罕见的元古代档案,将低硫酸盐浅海环境下的环境转变、微生物活动和成岩成矿作用联系起来,填补了全球δ34S数据集的关键地理和时间空白,并为早期地球氧化还原演化提供了新的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Grain-scale δ34S zonation in pyrite from the Chilpi Basin, India: Evidence for closed-system microbial sulfate reduction in the Proterozoic
This study presents the first documentation of stromatolitic carbonates from the Chilpi Basin, a Proterozoic volcano-sedimentary succession within the Bastar Craton of central India. The succession records a transition from shallow clastic to chemogenic sedimentation, with micritic limestone interbedded with syn-sedimentary barite and hosting domal stromatolites, overlain by phyllite. Euhedral diagenetic pyrite, disseminated within these microbialites, preserves a high-resolution archive of microbial and geochemical processes in a dynamic shallow marine environment. A total of 107 in situ sulfur isotope (34S/32S) analyses were conducted on pyrite grains using large-geometry Secondary Ion Mass Spectrometry (SIMS; CAMECA IMS-1300 HR3), yielding δ34SV-CDT values from +22.9 ‰ to +33.5 ‰. Larger grains exhibit clear intra-crystal zonation, with 34S-enriched rims relative to lighter cores (+25.5 ‰ to +33.5 ‰), consistent with Rayleigh distillation by microbial sulfate reduction (MSR) under semi-closed diagenetic conditions. Smaller grains show minimal internal variation, reflecting grain-specific histories within localized redox microenvironments. Rayleigh modeling indicates ∼41 % depletion of the original sulfate reservoir during pyrite growth. Petrographic and BSE imaging reveal features such as calcite–quartz overgrowths and magnetite rims, supporting a two-stage diagenetic growth of pyrite, followed by partial oxidation and replacement by magnetite. Stratiform barite within stromatolitic laminae records pulses of barium and sulfate availability under oxic to sub-oxic conditions, likely linked to episodic volcanic or hydrothermal input, while subsequent pyrite and magnetite document a progression through reducing to re-oxidizing conditions. This mineralogical sequence—from barite to pyrite to magnetite—captures a complete redox cycle at the grain scale. The Chilpi Basin thus provides a rare Proterozoic archive, resolved by SIMS, that links environmental transitions, microbial activity, and diagenetic mineralization in a low-sulfate shallow marine setting, filling a critical geographic and temporal gap in global δ34S datasets and offering new insight into early Earth redox evolution.
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来源期刊
Chemical Geology
Chemical Geology 地学-地球化学与地球物理
CiteScore
7.20
自引率
10.30%
发文量
374
审稿时长
3.6 months
期刊介绍: Chemical Geology is an international journal that publishes original research papers on isotopic and elemental geochemistry, geochronology and cosmochemistry. The Journal focuses on chemical processes in igneous, metamorphic, and sedimentary petrology, low- and high-temperature aqueous solutions, biogeochemistry, the environment and cosmochemistry. Papers that are field, experimentally, or computationally based are appropriate if they are of broad international interest. The Journal generally does not publish papers that are primarily of regional or local interest, or which are primarily focused on remediation and applied geochemistry. The Journal also welcomes innovative papers dealing with significant analytical advances that are of wide interest in the community and extend significantly beyond the scope of what would be included in the methods section of a standard research paper.
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