New constraints on fluid chemistry and elemental mobility during hydrothermal alteration from thallium isotope systematics of the battle mountain district, North-central Nevada

IF 3.1 3区 地球科学 Q1 GEOCHEMISTRY & GEOPHYSICS Applied Geochemistry Pub Date : 2023-09-01 DOI:10.1016/j.apgeochem.2023.105758
Shelby T. Rader , Caleb A. King , Mark D. Barton , Frank K. Mazdab
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引用次数: 1

Abstract

The Battle Mountain area is a major porphyry style Au (–Cu) district in northern Nevada, forming one end of the Battle Mountain-Eureka mineral trend. This trend, along with several others in the north-central Nevada region, hosts some of the world's most prolific gold mineralization, which is oftentimes associated with a suite of trace elements including arsenic, antimony, tungsten, and thallium and can be related to or overprinted by hydrothermal alteration. However, determining the extent of control hydrothermal fluids exert on some of the deposits in the region has been difficult to ascertain. One of the associated trace metals in the region, thallium (Tl), is a highly incompatible element and, as such, dominantly resides in the continental crust, where it can be easily remobilized during hydrothermal alteration. While previous work has demonstrated the effects of hydrothermal alteration on Tl distribution and fractionation, the controls responsible for the observed Tl fractionation during hydrothermal alteration are still poorly characterized but may provide insight into fluid behavior. Here, we present new Tl isotope composition and concentration data for a suite of 54 mineral separates obtained from 43 samples from the Battle Mountain area, which range from unaltered intrusive igneous rocks through varying types and degrees of hydrothermally altered rocks.

Measured Tl concentrations vary by more than an order of magnitude, from below detection limit (0.2 ppm in this study) to 2.0 ppm, while ε205Tl ranges between −5.0 and +2.2 (ε205Tl is the deviation of the 205Tl/203Tl isotope ratio of a sample from a standard in parts per 104). Thallium concentrations correlate positively with whole-rock potassium (K), thus show strong increases during K alteration, and demonstrate significantly lower ε205Tl values within K-altered samples. Conversely, during later, overprinting Na–Ca alteration, both K and Tl are removed, resulting in a noted decrease in Tl concentrations coupled with a shift to significantly higher ε205Tl values. It appears that during hydrothermal alteration, 203Tl is more easily (re)mobilized and (re)distributed, which reflects: 1) a first-order hydrothermal alteration control that relates to the transport of Tl during the formation of a new, metasomatic mineral assemblage (particularly the breakdown and/or formation of K-bearing minerals) and 2) a second-order mineralogical control, relating to inter-mineral equilibrium, which also results in a small fractionation effect.

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内华达中北部战山地区铊同位素系统对热液蚀变流体化学和元素迁移的新约束
巴特尔山地区是内华达州北部一个主要的斑岩型金(铜)带,形成巴特尔山—尤里卡矿物走向的一端。这一趋势,以及内华达地区中北部的其他几个趋势,拥有世界上最丰富的金矿化,这些金矿化通常与砷、锑、钨和铊等一系列微量元素有关,可能与热液蚀变有关或被热液蚀变覆盖。然而,热液流体对该地区某些矿床的控制程度一直难以确定。该地区伴生的微量金属之一铊(Tl)是一种高度不相容的元素,因此,它主要存在于大陆地壳中,在热液蚀变过程中很容易再活化。虽然以前的工作已经证明了热液蚀变对Tl分布和分馏的影响,但热液蚀变过程中观察到的Tl分馏的控制因素仍然没有得到很好的表征,但可能为流体行为提供见解。在这里,我们提供了从巴特尔山地区的43个样品中获得的54种矿物分离物的新的Tl同位素组成和浓度数据,这些样品从未蚀变的侵入火成岩到不同类型和程度的热液蚀变岩石。测量到的Tl浓度变化超过一个数量级,从低于检测限(本研究为0.2 ppm)到2.0 ppm,而ε205Tl的范围在- 5.0和+2.2之间(ε205Tl是样品的205Tl/203Tl同位素比值与标准的偏差,单位为104)。铊浓度与全岩钾(K)呈显著正相关,在钾蚀变过程中表现出较强的增加,且在钾蚀变样品中表现出较低的ε205Tl值。相反,在后期的复印Na-Ca蚀变过程中,K和Tl都被去除,导致Tl浓度显著降低,同时ε205Tl值显著升高。在热液蚀变过程中,203Tl更容易(再)调动和(再)分布,这反映了:1)在新的交代矿物组合形成过程中(特别是含钾矿物的破碎和/或形成过程),与Tl的输运有关的一级热液蚀变控制;2)与矿物间平衡有关的二级矿物学控制,这也导致了较小的分选效应。
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来源期刊
Applied Geochemistry
Applied Geochemistry 地学-地球化学与地球物理
CiteScore
6.10
自引率
8.80%
发文量
272
审稿时长
65 days
期刊介绍: Applied Geochemistry is an international journal devoted to publication of original research papers, rapid research communications and selected review papers in geochemistry and urban geochemistry which have some practical application to an aspect of human endeavour, such as the preservation of the environment, health, waste disposal and the search for resources. Papers on applications of inorganic, organic and isotope geochemistry and geochemical processes are therefore welcome provided they meet the main criterion. Spatial and temporal monitoring case studies are only of interest to our international readership if they present new ideas of broad application. Topics covered include: (1) Environmental geochemistry (including natural and anthropogenic aspects, and protection and remediation strategies); (2) Hydrogeochemistry (surface and groundwater); (3) Medical (urban) geochemistry; (4) The search for energy resources (in particular unconventional oil and gas or emerging metal resources); (5) Energy exploitation (in particular geothermal energy and CCS); (6) Upgrading of energy and mineral resources where there is a direct geochemical application; and (7) Waste disposal, including nuclear waste disposal.
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