铂族元素组成和铂族矿物组合对镁铁-超镁铁质岩浆成岩成矿作用的指示
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1.中国地质大学(武汉);2.中国科学院广州地球化学研究所;3.中国地质大学武汉

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国家自然科学基金项目(面上项目,重点项目,重大项目)


Genesis and significance of platinum-group element compositions and platinum-group mineral assemblages in magmatic processes and mineralization of mafic-ultramafic systems
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1.China University of Geosciences, Wuhan;2.Guangzhou Institute of Geochemistry, Chinese Academy of Sciences;3.Guangzhou Institute of Geochemistry,Chinese Academy of Sciences;4.School of Earth Resources,China University of Geosciences,Wuhan

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    摘要:

    镁铁-超镁铁质岩体及相关岩浆矿床的铂族元素(PGE)组成和铂族矿物(PGM)组合是地幔部分熔融、幔源镁铁-超镁铁质岩浆分离结晶、硫化物熔体分异和迁移等过程综合作用的产物,因此,可用来反演镁铁-超镁铁质岩浆的成岩成矿过程。本文通过一些研究实例探讨了蛇绿岩地幔橄榄岩、豆荚状铬铁矿矿床和岩浆铜镍硫化物矿床中岩石和矿石的PGE配分型式和PGM组成及其成因指示。实例一为土耳其K?z?lda?蛇绿岩中方辉橄榄岩的成因,该方辉橄榄岩的PGE含量为18.2×10-9~39.7×10-9,其中Os,Ir和Ru的含量变化范围小,而Pd和Pt变化范围较大,且Pd/Ir和Pt/Ir比值均大于1,在原始地幔标准化的PGE配分图上其PGE呈平坦型的配分模式,经模拟计算得出其是亏损地幔经20%部分熔融和熔-岩反应共同作用的产物。实例二为Kizilda?蛇绿岩中豆荚状铬铁矿矿床的形成过程,该矿床中不同矿石的铬铁矿内部均包裹自形-半自形的高Ru硫钌锇矿和Os-Ir合金,暗示铬铁矿结晶的温度约为1100~1200℃,硫逸度(log?S2)为-2~-1;而豆状矿石中铬铁矿粒间的PGM组合为Ru-Os纳米颗粒+Ru-Os纳米合金+FeNi3合金+磁铁镍矿(Fe2NiO4),其中FeNi3合金被磁铁镍矿所包围,表明铬铁矿在形成之后先经历低程度蛇纹石化过程后、又经历了快速的氧化过程,条带状和块状矿石中铬铁矿的粒间矿物组合为高Os硫钌锇矿+Os-Ir(Ru)合金/氧化物+氧化的镍黄铁矿+针镍矿(NiS),则暗示铬铁矿在形成之后经历了高程度蛇纹石化作用。实例三为美国Stillwater杂岩体中J-M Reef中发现的新矿物王焰钯矿(wangyanite)的成因指示,该矿物为极富Pd的镍黄铁矿族矿物,其Pd含量高达9.64%~10.59%,其与PGM和其他贱金属硫化物的结构关系表明,该矿物是演化的硫化物熔体与铂族矿物之间高温反应的产物,而不是单硫化物固溶体(MSS)或者中间硫化物固溶体(ISS)的出溶产物,上述实例研究表明,对镁铁-超镁铁质岩体及相关岩浆矿床中岩石和矿石的PGE配分型式和PGM组合展开系统研究,不仅可为研究岩浆矿床的物理化学条件提供新思路,也可对岩浆成矿过程提供更好的约束。

    Abstract:

    The compositions of platinum-group elements (PGE) and the assemblages of platinum-group minerals (PGMs) in mafic-ultramafic rocks and related magmatic deposits are the results of diverse processes, such as mantle partial melting, fractional crystallization of mafic-ultramafic magmas, and the segregation and migration of sulfide melts. Therefore, PGE and PGM can be used to reveal the processes of magmatic differentiation and ore formation. Here, we introduce some case studies showing that PGE partitioning pattern and PGM assemblages can indicate the formation and evolution of ophiolitic peridotite, podiform chromitite and magmatic sulfide deposit. Firstly, in the harzburgites of K?z?lda? ophiolite from Türkiye, the total content of PGE ranges from 18.15 to 39.65 ×10-9, with narrow ranges of Os, Ir and Ru, variable ranges of Pd and Pd, and high Pd/Ir and Pt/Ir ratios. All harzburgite samples have consistent and relatively flat PGE patterns when normalized to the primitive mantle. Base on PGE and trace element compositions and quantitative models, we concluded that the harzburgites of K?z?lda? ophiolite are the products of 20% partial melting of primary mantle and melt-rock interaction. Secondly, the PGM assemblages in different types of chromitite from K?z?lda? ophiolite are different. In all chromitite samples, primary laurite and Os-Ir alloy are typically enclosed within chromite, suggesting the crystallization of chromite at temperature of 1100–1200℃ and log?S2 values of -2 to -1. However, in nodular ores, Os-Ru nanoparticle + OsRu3 nanoalloy + awaruite (FeNi3) + trevorite (Fe2NiO4) are located in the intergranular space of chromite, indicating that the nodular chromitite underwent weak serpentinization and had low water/rock ratios (<~1), fS2 and fO2. On the other hand, in banded and massive chromitite, Os-rich laurite + Os-Ir(Ru) alloy/oxide + pentlandite + millerite (NiS) are located in the intergranular space of chromite, suggesting high water/rock ratios and high fS2 and fO2 during serpentinization. Thirdly, in the J-M reef of the Stillwater Complex, Montana, USA, we discovered a new mineral, Wangyanite. Wangyanite is a Pd end-member mineral of the pentlandite group, which has 9.64-10.59% Pd. Based on the textural features and previous experimental Pd-Fe-Ni-S phase system, wangyanite could form by peritectic reaction between braggite, pentlandite and sulfide liquid, rather than exsolved from monosulfide solid solution (MSS) and intermediate solid solution (ISS). To sum up, the studies of PGE compositions and PGM assemblages can provide new information on the magmatic deposit formation process and mechanism.

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  • 收稿日期:2025-10-28
  • 最后修改日期:2025-12-25
  • 录用日期:2026-01-04
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