Chalcophile and siderophile element (CSE) partitioning between sulfide liquid and silicate melt and the role of the “Hadean matte”

IF 3.6 2区 地球科学 Q1 GEOCHEMISTRY & GEOPHYSICS
Mingdong Zhang , Yuan Li
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引用次数: 0

Abstract

This study evaluates the role of mantle-to-core segregation of the “Hadean matte” (sulfide liquids) occurring in the solidifying magma ocean in determining the chalcophile and siderophile element (CSE) abundances of the silicate Earth. The partition coefficients of CSEs between sulfide liquid and basaltic to peridotitic melt (DCSESul/Sil) were determined at 1–14 GPa and 1300–2100 °C. The variations in the obtained DCSESul/Sil (30–160 for Co, 50–1200 for Ni, 40–940 for Cu, 20–210 for Mo, 50–210 for Ag, 20–90 for Cd, 4–60 for In, 30–150 for Sb, 3900–30,000 for Re, 15–210 for Pb, 140–1700 for Bi, 0.3–7 for Zn, 0.7–7 for Ge, and 0.1–0.9 for Ga) can be explained and parameterized as a function of the experimental pressure, temperature, and composition of the silicate melt and sulfide liquid. Application of the DCSESul/Sil parameterization to the mantle-to-core segregation of sulfide liquids in a deep magma ocean at 75 GPa shows that less than 10 % of each of Co, Ni, Cu, Zn, Ga, Ge, Mo, Ag, Cd, In, Sb, Pb, and Bi in the silicate Earth can be sequestered in the core; whereas, in a shallow magma ocean at 10 GPa, 50–80 % of each of Cu, Ag, and Bi and less than 50 % of the other CSEs can be sequestered in the core. In contrast, mantle-to-core segregation of sulfide liquids could have extracted more than 90 % of the Re in the silicate Earth in both cases, requiring the addition of a late veneer to explain the present-day mantle value. Our results demonstrate that if Earth's volatile CSEs (Cu, Zn, Ga, Ge, Ag, Cd, In, Sb, Pb, and Bi) were delivered when metal segregation to the core was largely inactive, the depletion pattern of volatile CSEs relative to the lithophile elements of similar volatility in the silicate Earth cannot be explained by mantle-to-core segregation of sulfide liquids. Also, previous models that used mantle-to-core segregation of sulfide liquids as an important approach to explain the depletion of volatile CSEs in the silicate Earth need to be re-examined.
硫化物液体与硅酸盐熔体中亲铜亲铁元素(CSE)的分配及冥古宙物质的作用
本研究评价了凝固岩浆海洋中发生的“冥古宙matte”(硫化物液体)的幔核分离在确定硅酸盐地球中亲铜和亲铁元素(CSE)丰度中的作用。测定了硫化液与玄武岩/橄榄岩熔体(DCSESul/Sil)在1 ~ 14 GPa和1300 ~ 2100℃条件下的分配系数。所得的DCSESul/Sil的变化(Co为30-160,Ni为50-1200,Cu为40-940,Mo为20-210,Ag为50-210,Cd为20-90,in为4-60,Sb为30-150,Re为3900-30,000,Pb为15-210,Bi为140-1700,Zn为0.3-7,Ge为0.7-7,Ga为0.1-0.9)可以解释和参数化为实验压力,温度和硅酸盐熔体和硫化物液体组成的函数。应用dscsesul /Sil参数化方法对75 GPa深部岩浆海中硫化物液体的幔核分离分析表明,硅酸盐土中Co、Ni、Cu、Zn、Ga、Ge、Mo、Ag、Cd、in、Sb、Pb、Bi等元素在岩心中被隔离的比例均小于10%;而在10 GPa的浅层岩浆海中,Cu、Ag和Bi的50 - 80%和其他cse的不到50%可以被隔离在地核中。相比之下,在这两种情况下,硫化物液体从地幔到地核的分离可以提取硅酸盐地球中90%以上的稀土,这就需要添加一个后期的贴片来解释当今的地幔价值。我们的研究结果表明,如果地球的挥发性铯元素(Cu、Zn、Ga、Ge、Ag、Cd、In、Sb、Pb和Bi)是在金属偏析基本上不活跃的情况下被传递到岩心的,那么相对于具有相似挥发性的亲石元素,在硅酸盐地球中挥发性铯元素的耗损模式不能用硫化物液体的地幔-岩心偏析来解释。此外,以前的模型将硫化物液体的地核分离作为解释硅酸盐地球中挥发性cse耗竭的重要方法,需要重新检查。
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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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