曼尼托巴雪湖Lalor变质VHMS矿床中菱铁矿的矿物化学特征

IF 1.1 4区 地球科学 Q3 MINERALOGY
E. Wehrle, A. McDonald, D. Tinkham
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引用次数: 1

摘要

锌铝榴辉石(ZnAl2O4)是曼尼托巴雪湖Lalor含金锌铜变质VHMS矿床中常见的副矿物。为了评估影响其晶体化学的因素,研究人员分析了一系列结构、寄主矿物组合和整个岩石组成,包括主元素、微量元素和微量元素。所分析的晶粒分布在Ghn63-75Her15-22Spl10-18的范围内,锌、铁和镁的含量没有分区。镁元素与全岩MgO呈中等正相关(R2 = 0.66)。Lalor锌长晶石的微量元素和微量元素化学以Mn (400 ~ 2600 ppm)、Si (<25 ~ 250 ppm)和V (<25 ~ 2300 ppm)为主。基于锌矿主元素组成的有限变化,以及闪锌矿-锌矿对之间Zn和Fe的分配系数相似(表明所分析的锌矿的变质结晶条件相似),变质品位对锌矿主元素化学的影响最大。闪锌矿大多与黄铁矿和磁黄铁矿共生,这种组合可能缓冲了fS2,固定了闪锌矿中的Zn:Fe比值,这也可能导致闪锌矿的成分范围较窄。镁并不是消耗闪锌矿和产生锌锌矿反应的必需组分,因此镁在锌锌矿中的含量更容易受到全岩Mg的影响。一小部分辉长岩颗粒可能是由硅酸盐(橄榄石和黑云母)的失稳形成的,而不是闪锌矿。这些可能形成闪锌矿的反应(闪锌矿与黑云母或小沸石的消耗)似乎对闪锌矿的微量元素和微量元素化学具有最强的控制作用,因为闪锌矿脱硫反应形成的闪锌矿显示出Mn (450-2600 ppm)的范围和限制的V/Mn值(<0.5),而解释为由黑云母和小沸石脱水形成的闪锌矿显示出限制的Mn (<430 ppm)和V/Mn值(0.75-5.5)的范围。建议进一步研究利用闪锌矿微量元素特征(如Mn和V)来区分在富含闪锌矿和无闪锌矿环境中结晶的闪锌矿的可能性,因为这一概念有可能应用于利用碎屑闪锌矿进行勘探。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mineral chemistry of gahnite from the Lalor metamorphosed VHMS deposit, Snow Lake, Manitoba
Gahnite (ZnAl2O4) is a common accessory mineral at the Lalor auriferous Zn-Cu metamorphosed VHMS deposit (Snow Lake, Manitoba). To evaluate factors influencing its crystal chemistry, gahnite representing a range of textures, host mineral assemblages, and whole-rock compositions were analyzed for major, minor, and trace elements. The analyzed grains span the range of Ghn63-75Her15-22Spl10-18 and are un-zoned with respect to Zn, Fe, and Mg. A moderate positive correlation exists between Mg in gahnite and whole-rock MgO (R2 = 0.66). The minor- and trace-element chemistry of the Lalor gahnite is dominated by Mn (400–2600 ppm), Si (<25–250 ppm), and V (<25–2300 ppm). Based on the limited variability in gahnite major-element composition, as well as similar partitioning coefficients of Zn and Fe between sphalerite-gahnite pairs (indicating comparable metamorphic conditions of crystallization for the analyzed gahnite), metamorphic grade is interpreted to have had the strongest influence on gahnite major-element chemistry. Most sphalerite occurs with pyrite and pyrrhotite, an assemblage that would have buffered fS2 and fixed the Zn:Fe ratio in sphalerite, which also could have contributed to the narrow compositional range observed in gahnite. Magnesium was not an essential component of the sphalerite-consuming, gahnite-producing reactions, so its concentration in gahnite was more readily affected by whole-rock Mg. A small proportion of gahnite grains may have formed from the destabilization of silicates (staurolite and biotite), rather than sphalerite. These possible gahnite-forming reactions (sphalerite- versus biotite- or staurolite-consuming) appear to have had the strongest control on gahnite minor- and trace-element chemistry, as gahnite formed from sphalerite desulfidation reactions shows a range in Mn (450–2600 ppm) and restricted V/Mn values (<0.5), while gahnite interpreted to have formed from the dehydration of biotite and staurolite shows restricted Mn (<430 ppm) and a range of V/Mn values (0.75–5.5). Further work is recommended to investigate the possibility of using gahnite trace-element signatures (such as with Mn and V) to discriminate between gahnite that crystallized in sphalerite-rich and sphalerite-barren environments, as this concept has potential for application to exploration using detrital gahnite.
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来源期刊
Canadian Mineralogist
Canadian Mineralogist 地学-矿物学
CiteScore
2.20
自引率
22.20%
发文量
45
审稿时长
4-8 weeks
期刊介绍: Since 1962, The Canadian Mineralogist has published papers dealing with all aspects of mineralogy, crystallography, petrology, economic geology, geochemistry, and applied mineralogy.
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