Fe and Mg isotopes as tracers of the mantle sources and ore-forming processes of the Xiarihamu magmatic Ni-Cu sulfide deposit

IF 2.9 2区 地球科学 Q2 GEOCHEMISTRY & GEOPHYSICS
Qingyan Tang , Yan Zhang , Lu Li , Zhaowei Zhang , Zhuoming Li , Wei Liu , Chi Zhao , Tengda Yang , Tianyu Qin
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Abstract

Mg and Fe isotopes increasingly are utilized to investigate the origins of magmatic sulfide deposits and interactions between the crust and mantle. However, further evaluation of the validity of using Fe isotopes as a constraint to assess crustal contamination is necessary, particularly using more mafic-ultramafic samples. To address this issue, we analyzed the Mg and Fe isotopic compositions of silicate and sulfide minerals in the Xiarihamu magmatic Ni-Cu sulfide deposit, which has high Ni reserves and is located in the East Kunlun Orogenic Belt. The clinopyroxene and orthopyroxene separates from the Xiarihamu deposit have δ56Fe values of −0.048 ‰ to +0.172 ‰ and a Δ56FeCpx-Opx value of 0.068 ‰. The pentlandite separates have δ56Fe values of −0.475 ‰ to +0.062 ‰ and Δ56FeOpx-Pn values of −0.001 ‰ to 0.487 ‰. The clinopyroxene and orthopyroxene separates have δ26Mg values of −0.376 ‰ to −0.141 ‰ and a Δ26MgOpx-Cpx value of −0.014 ‰. Most of the δ26Mg values of the silicate minerals align with those of unmodified mantle. The observed Fe and Mg isotope variations of the minerals in this deposit exceed those caused by mantle melting. The δ56Fe and δ26Mg values of the mineral separates do not exhibit correlations with the whole-rock loss on ignition (LOI), orthopyroxene Mg/(Mg + Fe) molar ratio, olivine forsterite content, and sulfide δ34S, indicating that post-magmatic hydrothermal alteration, crystallization differentiation, and crustal sulfur addition cannot sufficiently explain the Mg and Fe isotope variations in the Xiarihamu deposit. The δ26Mg and δ56Fe values are lower than mantle values, indicating that the mantle source was modified by a carbonate melt. The δ56Fe values exhibit a weak positive correlation with the fO2 value, and the relationship between the Pd tenor and δ56Fe value is consistent with the variations in the silicate melt to sulfide liquid mass ratio (R factor), illustrating that the Fe isotope variations in the Xiarihamu deposit were controlled by both the redox conditions and R factor. The Mg-Sr-Nd mixing calculations revealed that crustal assimilation was crucial for triggering the sulfide saturation in the Xiarihamu deposit. Therefore, Fe isotopes may be unsuitable for identifying crustal contamination; however, when combined with Mg isotopes, they can be useful in determining the mantle sources and metallogenic processes in igneous Ni-Cu mineralization systems. These findings have important implications for future research on the formation of Ni-Cu sulfide deposits, and the mechanisms of Fe isotope fractionation.
下日哈木岩浆镍铜硫化物矿床地幔源及成矿过程的铁、镁同位素示踪
镁和铁同位素越来越多地用于研究岩浆硫化物矿床的起源和壳幔之间的相互作用。然而,有必要进一步评估使用铁同位素作为评估地壳污染约束的有效性,特别是使用更多的镁铁质-超镁铁质样品。为解决这一问题,对东昆仑造山带下日哈木镍铜岩浆硫化物矿床中硅酸盐矿物和硫化物矿物的Mg、Fe同位素组成进行了分析。下日哈木矿床斜辉石和正辉石分离物的δ56Fe值为−0.048‰~ +0.172‰,Δ56FeCpx-Opx值为0.068‰。其δ56Fe值为−0.475‰~ +0.062‰,Δ56FeOpx-Pn值为−0.001‰~ 0.487‰。斜辉石和正辉石分离物的δ26Mg值为−0.376‰~−0.141‰,Δ26MgOpx-Cpx值为−0.014‰。大部分硅酸盐矿物的δ26Mg值与未变质地幔的δ26Mg值一致。该矿床矿物的铁、镁同位素变化超出了地幔熔融引起的变化。矿物分离物的δ56Fe和δ26Mg值与全岩着火损失(LOI)、正辉石Mg/(Mg + Fe)摩尔比、橄榄石forsterite含量和硫化物δ34S没有相关性,表明岩浆后热液蚀变、结晶分异和地壳硫添加不能充分解释下日哈木矿床Mg和Fe同位素的变化。δ26Mg和δ56Fe值均低于地幔值,表明地幔源受到碳酸盐熔体的改造。δ56Fe值与fO2值呈弱正相关,Pd值与δ56Fe值的关系与硅酸盐熔体与硫化物液体质量比(R因子)的变化一致,说明下日哈木矿床的Fe同位素变化受氧化还原条件和R因子的双重控制。Mg-Sr-Nd混合计算表明,地壳同化作用是引发下日哈木矿床硫化物饱和的关键因素。因此,铁同位素可能不适合识别地壳污染;然而,当与Mg同位素结合时,它们可以用于确定火成岩镍铜成矿系统的地幔来源和成矿过程。这些发现对今后研究镍铜硫化物矿床的形成及铁同位素分馏机理具有重要意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Lithos
Lithos 地学-地球化学与地球物理
CiteScore
6.80
自引率
11.40%
发文量
286
审稿时长
3.5 months
期刊介绍: Lithos publishes original research papers on the petrology, geochemistry and petrogenesis of igneous and metamorphic rocks. Papers on mineralogy/mineral physics related to petrology and petrogenetic problems are also welcomed.
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