川西毛湾里锰矿床中草莓状黄铁矿特征对沉积环境及成矿机理的指示

    Characteristics of framboidal pyrite for implications of sedimentary environment and mineralization mechanism in the Maowanli manganese deposit, Western Sichuan

    • 摘要:
      研究目的 近年来龙门山构造带沉积型锰矿勘查取得了重大突破,但存在沉积环境不清晰、Mn元素富集机制不明确等问题。为了探究以上问题,以龙门山构造带毛湾里锰矿床为研究对象,对该地区的沉积环境及Mn富集机制展开研究。
      研究方法 在详细的野外地质调查和室内光薄片鉴定的基础上,系统统计了含矿岩系黄铁矿的形态学特征,对黄铁矿的粒径进行统计分析。
      研究结果 毛湾里锰矿含矿岩系为下寒武统邱家河组一段,岩性主要包括硅质岩、黑色板岩、白云岩、含锰黑色硅质白云岩、黄铁矿层和含锰岩系。含锰岩系中矿石矿物主要为锰白云石、硫锰矿和少量含锰方解石、菱锰矿,脉石矿物包括石英、白云石和黄铁矿,含少量胶磷矿、重晶石和有机质。含锰岩系草莓状黄铁矿发育,其粒径统计结果含锰岩系中为1.38~31.05 μm,平均5.18 μm;黄铁矿层中为1.60~28.42 μm,平均6.73 μm;黑色板岩中为1.31~31.34 μm,平均值为6.60 μm;含锰黑色硅质白云岩中为3.14~23.20 μm,平均6.74 μm;白云岩中为0.88~7.03 μm;硅质岩中为1.73~22.83 μm,平均6.03 μm。整体上,含矿岩系沉积于次氧化-缺氧-硫化的底层水条件下。
      结论 由于Mn(Ⅱ)向Mn(Ⅳ)的转变发生于氧化—次氧化界面,且矿石中未见锰的氧化物,推测Mn的富集沉淀与BSR(生物硫氧化还原菌)作用及EPS(胞外聚合物)关系密切:①次氧化—缺氧底层水条件下,生物有机质沉降,并发生BSR作用,释放CO32−和H2S进入孔隙水和底层水;②胞外聚合物(EPS)吸附Mg2+、Mn2+、Ca2+和CO32−,提供锰白云石的成核位点,诱导锰白云石的大量沉淀,并在埋藏过程中进一步外延生长;③BSR释放进入底层水的H2S优先与Fe2+离子结合,形成草莓状黄铁矿,剩余H2S在孔隙水中与Mn2+离子结合形成硫锰矿。

       

      Abstract:
      Objective In recent years, significant breakthroughs have been achieved in the exploration of sedimentary manganese deposits within the Longmenshan tectonic belt. However, problems such as an unclear sedimentary environment and ambiguous manganese enrichment mechanisms persist. To address these issues, this study focuses on the Maowanli manganese deposit in the Longmenshan tectonic belt to further investigate the regional sedimentary environment and enrichment mechanisms.
      Methods Based on detailed field geological surveys and indoor thin−section identification, the morphological characteristics of pyrite in the ore−bearing rock series were systematically documented, and statistical analysis of pyrite particle size was conducted.
      Results The ore−bearing rock series of the Maowanli manganese deposit belongs to the First Member of the Lower Cambrian Qiujiahe Formation. The lithology primarily includes siliceous rocks, black slate, dolomite, manganese−bearing black siliceous dolomite, pyrite layers, and manganese−bearing rock series. The primary ore minerals in the manganese−bearing series are dolomite and alabandite, with minor amounts of Mn−calcite and rhodochrosite. The gangue minerals consist of quartz, dolomite, and pyrite, with small amounts of collophane, barite, and organic matter. Framboidal pyrite is well−developed in the manganese−bearing series. The statistical results of particle sizes are as follows: in the manganese−bearing series, it ranges from 1.38 μm to 31.05 μm, with an average of 5.18 μm; in the pyrite layers, from 1.60 μm to 28.42 μm, averaging 6.73 μm; in black slate, from 1.31 μm to 31.34 μm, averaging 6.60 μm; in manganese−bearing black siliceous dolomite, from 3.14 μm to 23.20 μm, averaging 6.74 μm; in dolomite, from 0.88 μm to 7.03 μm; and in siliceous rocks, from 1.73 μm to 22.83 μm, averaging 6.03 μm. Overall, the ore−bearing series was deposited under dysoxic−subxic−euxinic bottom water conditions.
      Conclusions Given that the transformation from Mn(Ⅱ) to Mn(Ⅳ) occurs at the oxic−dysoxic interface and no manganese oxides are observed in the ore, it is inferred that manganese enrichment and precipitation are closely related to BSR (bacterial sulfate reduction) and EPS (extracellular polymeric substances): ① Under dysoxic−suboxic bottom water conditions, biological organic matter settled and underwent BSR, releasing CO32 and H2S into the pore water and bottom water; ② EPS adsorbed Mg2+, Mn2+, Ca2+, and CO32, providing nucleation sites for kutnohorite and inducing its massive precipitation, followed by further epitaxial growth during burial; ③ H2S released via BSR into the bottom water preferentially combined with Fe2+ to form framboidal pyrite, while the remaining H2S in the pore water combined with Mn2+ to form alabandite.

       

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