首页> 外文期刊>Acta Geologica Sinica - English Edition >Ore Genesis of the Kalatongke Cu–Ni Sulfide Deposits, Western China: Constraints from Volatile Chemical and Carbon Isotopic Compositions
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Ore Genesis of the Kalatongke Cu–Ni Sulfide Deposits, Western China: Constraints from Volatile Chemical and Carbon Isotopic Compositions

机译:中国西部卡拉通克铜镍硫化物矿床的矿石成因:挥发性化学成分和碳同位素组成的约束

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The Kalatongke Cu–Ni sulfide deposits located in the East Junggar terrane, northern Xinjiang, western China are the largest magmatic sulfide deposits in the Central Asian Orogenic Belt (CAOB). The chemical and carbon isotopic compositions of the volatiles trapped in olivine, pyroxene and sulfide mineral separates were analyzed by vacuum stepwise-heating mass spectrometry. The results show that the released volatiles are concentrated at three temperature intervals of 200–400°C, 400–900°C and 900–1200°C. The released volatiles from silicate mineral separates at 400–900°C and 900–1200°C have similar chemical and carbon isotopic compositions, which are mainly composed of H2O (av. ∼92 mol%) with minor H2, CO2, H2S and SO2, and they are likely associated with the ore-forming magmatic volatiles. Light δ13CCO2 values (from –20.86‰ to –12.85‰) of pyroxene indicate crustal contamination occurred prior to or synchronous with pyroxene crystallization of mantle-derived ore-forming magma. The elevated contents of H2 and H2O in the olivine and pyroxene suggest a deep mantle-originated ore-forming volatile mixed with aqueous volatiles from recycled subducted slab. High contents of CO2 in the ore-forming magma volatiles led to an increase in oxygen fugacity, and thereby reduced the solubility of sulfur in the magma, then triggered sulfur saturation followed by sulfide melt segregation; CO2 contents correlated with Cu contents in the whole rocks suggest that a supercritical state of CO2 in the ore-forming magma system under high temperature and pressure conditions might play a key role in the assemblage of huge Cu and Ni elements. The volatiles released from constituent minerals of intrusion 1* have more CO2 and SO2 oxidized gases, higher CO2/CH4 and SO2/H2S ratios and lighter δ13CCO2 than those of intrusions 2# and 3#. This combination suggests that the higher oxidation state of the volatiles in intrusion 1# than intrusions 2# and 3#, which could be one of key ore-forming factors for large amounts of ores and high contents of Cu and Ni in intrusion 1#. The volatiles released at 200–400°C are dominated by H2O with minor CO2, N2+CO and SO2, with δ13CCO2, values (–25.66‰ to –22.98‰) within the crustal ranges, and are considered to be related to secondary tectonic– hydrothermal activities.
机译:位于中国西部新疆北部准Jung尔东部的卡拉通克铜镍硫化物矿床是中亚造山带(CAOB)中最大的岩浆硫化物矿床。通过真空逐步加热质谱法分析了橄榄石,辉石和硫化物矿物分离物中捕获的挥发物的化学和碳同位素组成。结果表明,释放的挥发物在200-400°C,400-900°C和900-1200°C的三个温度间隔内浓缩。在400–900°C和900–1200°C下从硅酸盐矿物分离物中释放的挥发物具有相似的化学和碳同位素组成,主要由H 2 O组成(av。〜92 mol%)具有次要的H 2 ,CO 2 ,H 2 S和SO 2 ,并且它们可能与成矿岩浆挥发物。辉石的轻δ 13 C CO2 值(从–20.86‰至–12.85‰)表明地壳污染发生在地幔衍生的成矿的辉石结晶之前或与之同步。岩浆。橄榄石和辉石中H 2 和H 2 O的含量升高,表明形成了深地幔的成矿挥发物与回收的俯冲板中的含水挥发物混合在一起。成矿的岩浆挥发物中CO 2 含量高,导致氧逸度增加,从而降低了硫在岩浆中的溶解度,进而引起硫饱和,随后硫化物熔体偏析。整个岩石中CO 2 含量与Cu含量相关,表明成矿岩浆系统中高温高压条件下CO 2 超临界状态可能起关键作用。在巨大的铜和镍元素的组合中发挥重要作用。从侵入岩1 *的构成矿物释放的挥发物具有更多的CO 2 和SO 2 氧化气体,更高的CO 2 / CH 4 和SO 2 / H 2 S比和δ 13 C CO2 比入侵更轻2 #和3 #。这种结合表明入侵1 #中挥发物的氧化态比入侵2 #和3 #高,这可能是关键之一入侵1 #中大量矿石和高含量Cu,Ni的成矿因素。在200–400°C下释放的挥发物主要由H 2 O和少量的CO 2 ,N 2 + CO和SO 2 ,δ 13 C CO2 ,其值(–25.66‰至–22.98‰)在地壳范围内,并被认为与次生构造有关–热液活动。

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