First-principles investigations of equilibrium calcium isotope fractionation between clinopyroxene and Ca-doped orthopyroxene

被引:72
|
作者
Feng, Chongqin [1 ,2 ]
Qin, Tian [2 ,3 ]
Huang, Shichun [4 ]
Wu, Zhongqing [2 ,3 ]
Huang, Fang [1 ]
机构
[1] Univ Sci & Technol China, Sch Earth & Space Sci, CAS Key Lab Crust Mantle Mat & Environm, Hefei 230026, Anhui, Peoples R China
[2] Univ Sci & Technol China, Sch Earth & Space Sci, Lab Seismol & Phys Earths Interior, Hefei 230026, Anhui, Peoples R China
[3] Mengcheng Natl Geophys Observ, Mengcheng, Anhui, Peoples R China
[4] Univ Nevada, Dept Geosci, Las Vegas, NV 89154 USA
基金
美国国家科学基金会;
关键词
RIO-GRANDE RIFT; HIGH P; MINERALS; OXYGEN; TEMPERATURE; ELEMENT; CARBON; LI; PSEUDOPOTENTIALS; DELTA-CA-44/40;
D O I
10.1016/j.gca.2014.06.002
中图分类号
P3 [地球物理学]; P59 [地球化学];
学科分类号
0708 ; 070902 ;
摘要
Equilibrium fractionation factors of Ca isotopes among mantle minerals are essential for using Ca isotopes as an important tracer in mantle geochemistry. Using the vibrational frequencies obtained by the first-principles calculations based on density functional theory (DFT), we calculated equilibrium fractionation factors of Ca isotopes between two major Ca-bearing minerals, clinopyroxene (cpx) and orthopyroxene (opx). Our results show that opx has much higher Ca-44/Ca-40 than its co-existing cpx even at high temperatures (e.g., 1273 K), agreeing with the observations on mantle peridotites. In addition to the well-known temperature effect, our calculations for the first time reveal that the inter-mineral Ca isotope fractionation factor between opx and cpx also has a strong dependence on the chemical composition of opx (i.e., Ca content). Specifically, it increases substantially with decreasing Ca/Mg (atomic ratio) of opx when Ca/Mg-opx is lower than 1/15. Such compositional effect on inter-mineral Ca isotope fractionation provides a convincing interpretation to the different isotope fractionations between coexisting opx and cpx observed in Kilbourne Hole and San Carlos peridotites. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:132 / 142
页数:11
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