利用造山SbAu矿床碳酸盐的CMg同位素组合组成作为流体与海底蚀变地壳相互作用的示踪剂

IF 3.6 2区 地球科学 Q1 GEOCHEMISTRY & GEOPHYSICS
Andrea Agangi , Axel Hofmann , Takuya Echigo , Robert Bolhar , Daisuke Araoka , Vincent Mashoene , Lucia T. Ndhlovu , Ryohei Takahashi , Pearlyn C. Manalo
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引用次数: 0

摘要

中太古代Murchison绿岩带位于非洲南部Kaapvaal克拉通北部,由变质至角闪岩相的强烈变形火山-沉积序列组成,并被含铝质和过铝质花岗岩类包围。沿绿岩带(WSW-ENE)主走向,长约40公里的强碳酸盐岩剪切带(锑线,或称锑线)拥有重要的锑矿床,伴生有金。这些商品主要以辉锑矿和天然金的形式赋存于sb线中心的石英-碳酸盐岩中,强调了变形和变质过程中富co2流体流动对成矿作用的重要性。在这项研究中,我们比较了来自sb线的碳酸盐的元素和稳定同位素(C-O-Mg)组成与远矿化的火山-沉积演替所承载的区域分布的碳酸盐。sb线碳酸盐与区域岩石主要元素组成重叠。大多数Sb-Line样品中的菱镁矿和白云石都有明显的轻稀土耗尽模式,并伴有变化的Eu正异常。碳同位素比值定义了两个簇,其中sb线岩石的δ13C峰值约为-5‰,区域岩石的δ13C峰值约为-2‰,表明存在不同的碳源。-2‰的第一个峰值可能代表了海底蚀变的早期碳化作用,而-5‰的第一个峰值则表明了sb线构造活动期间引入的深部二氧化碳(地幔或岩浆源)。区域岩石的镁同位素比值显示出有限的分选作用(整体δ26Mg = - 0.27±0.10‰),与地幔值重叠,但部分含碳酸盐脉体呈现贫镁成分(整体δ26Mg = - 1.91 ~ - 0.40‰)。sb线碳酸盐岩中Mg同位素组成分馏较多(δ26Mg = - 0.8‰~ - 0.0‰),碳酸盐岩的δ26Mg值为- 1.46‰~ - 0.31‰。我们将这些结果解释为同位素轻Mg在流体-岩石相互作用过程中的优先再活化和寄主岩石中碳酸盐的溶解。δ13C和δ26Mg之间缺乏相关性,表明这些同位素系统存在解耦,表明C和Mg的同位素来源不同,对矿化带有贡献。与太古宙绿岩带中其它受构造控制的AuSb矿化作用类似,Murchison绿岩带中的金属运输和矿石沉积与碳的深层循环密切相关,将海底蚀变过程中的碳下降、变质作用过程中的碳酸盐再动员和主要地壳不连续的深层CO2脱气联系在一起。与造山带AuSb矿床模型相比,我们的研究结果强调了来自火山-沉积演替的外部源的深源流体的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The use of combined CMg isotope compositions of carbonates from orogenic SbAu deposits as a tracer of fluid interaction with sea-floor altered crust
The Mesoarchaean Murchison Greenstone Belt is composed of a strongly deformed volcano-sedimentary succession metamorphosed up to amphibolite facies and surrounded by metaluminous and peraluminous granitoids in the north of the Kaapvaal Craton of southern Africa. A circa 40 km-long shear-zone of strongly carbonatised rocks (the Antimony Line, or Sb-Line) oriented along the main trend of the greenstone belt (WSW–ENE) hosts important Sb deposits with accessory Au. These commodities mostly occur as stibnite and native gold hosted by quartz‑carbonate rocks at the centre of the Sb-Line, underlining the importance of CO2-rich fluid flow for mineralisation during deformation and metamorphism.
In this study, we compare the elemental and stable isotope (C-O-Mg) composition of carbonates from the Sb-Line with regionally distributed carbonates hosted by the volcano-sedimentary succession distal to mineralisation. The carbonates of the Sb-Line and regional rocks have overlapping major element compositions. Both magnesite and dolomite in most Sb-Line samples have marked light-REE-depleted patterns with variable positive Eu anomalies. Carbon isotope ratios define two clusters, with marked δ13C peaks at ca. -5 ‰ for Sb-Line rocks and ca. -2 ‰ for regional rocks, implying separate C-sources. The peak at ca. -2 ‰ likely represents early carbonatisation through sea-floor alteration, whereas the first peak at ca. -5 ‰ is indicative of deep CO2 (mantle, or magma-derived) introduced during tectonic activity of the Sb-Line. Magnesium isotope ratios of regional rocks reveal limited fractionation (bulk δ26Mg = −0.27 ± 0.10 ‰) that overlap with mantle values, but some carbonate-bearing veins present 26Mg-depleted compositions (bulk δ26Mg = −1.91 to −0.40 ‰). Sb-Line carbonated rocks have more fractionated Mg isotope compositions (bulk δ26Mg = −0.8 to 0.0 ‰) and carbonates display marked negative 26Mg values (δ26Mg from −1.46 to −0.31 ‰). We interpret these results in terms of preferential remobilisation of isotopically light Mg during fluid-rock interaction and dissolution of carbonate in the host-rocks. The lack of correlation between δ13C and δ26Mg indicates decoupling of these isotopic systems, implying contribution from isotopically distinct sources of C and Mg to the mineralised zone.
Similar to other structurally controlled AuSb mineralisation in Archaean greenstone belts, metal transport and ore deposition in the Murchison Greenstone Belt was closely related to the deep cycle of carbon, linking C-draw-down during sea-floor alteration, carbonate re-mobilisation during metamorphism and CO2 degassing from deep sources along major crustal discontinuities. In contrast to models for orogenic AuSb deposits invoking a purely intra-crustal, metamorphic origin of mineralising fluids, our results underline the importance of deep-sourced fluids originating from an external source from the volcano-sedimentary succession.
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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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