Water in coesite: Incorporation mechanism and operation condition, solubility and P-T dependence, and contribution to water transport and coesite preservation
Yan, Wei3,5; Zhang, Yanyao6; Ma, Yunlu3,5; He, Mingyue1; Zhang, Lifei3,5; Sun, Weidong2; Wang, Christina Yan4; Liu, Xi3,5
刊名GEOSCIENCE FRONTIERS
2021
卷号12期号:1页码:313-326
关键词Coesite preservation FTIR New IR experimental Protocol Anhydrous minerals P-T dependence of water solubility Water-incorporation mechanism
ISSN号1674-9871
DOI10.1016/j.gsf.2020.05.007
通讯作者Liu, Xi(xi.liu@pku.edu.cn)
英文摘要A series of coesite, coexisting with or without a liquid phase, was synthesized in the nominal system SiO2-H2O at 800-1450 degrees C and 5 GPa. Micro-Raman spectroscopy was used to identify the crystalline phase, electron microprobe and LA-ICP-MS were employed to quantify some major and trace elements, and unpolarized FTIR spectroscopy was applied to probe the different types of hydrogen defects, explore water-incorporation mechanisms and quantify water contents. Trace amounts of Al and B were detected in the coesite. Combining our results with the results in the literatures, we have found no positive correlation between the Al contents and the "Al"-based hydrogen concentrations, suggesting that previously proposed hydrogen-incorporation mechanism H+ Al3+ <-> Si4+ does not function in coesite. In contrast, we have confirmed the positive correlation between the B contents and the B-based hydrogen concentrations. The hydrogen-incorporation mechanism H+ + B3+ <-> Si4+ readily takes place in coesite at different P-T conditions, and significantly increases the water content at both liquid-saturated and liquid-undersaturated conditions. For the SiO2-H2O system, we have found that type-I hydrogarnet substitution plays a dictating role in incorporating water into coesite at liquid-saturated condition, type-II hydrogarnet substitution contributes significantly at nearly dry condition, and both operate at conditions in between. The water solubility of coesite, as dictated by the type-I hydrogarnet substitution, positively correlates with both P and T, c(H)(2O) = -105(30) + 5.2(32) x P + 0.112(26) x T, with c(H)(2O) in wt ppm, P in GPa and T in degrees C. Due to its low water solubility and small fraction in subducted slabs, coesite may contribute insignificantly to the vertical water transport in subduction zones. Furthermore, the water solubility of any coesite in exhuming ultra-high pressure metamorphic rocks should be virtually zero as coesite becomes metastable. With an adequately fast water-diffusion rate, this metastable coesite should be completely dry, which may have been the key factor to the partial preservation of most natural Coe. As a byproduct, a new IR experimental protocol for accurate water determination in optically anisotropic nominally anhydrous minerals has been found. Aided with the empirical method of Paterson (1982) it employs multiple unpolarized IR spectra, collected from randomly-orientated mineral grains, to approximate both total integrated absorbance and total integrated molar absorption coefficient. Its success relies on a high-level orientation randomness in the IR analyses.
资助项目DREAM project of MOST, China[2016YFC0600408] ; Chinese Academy of Sciences[XDB18000000] ; Program of the National Mineral Rock and Fossil Specimens Resource Center from MOST, China
WOS研究方向Geology
语种英语
出版者CHINA UNIV GEOSCIENCES, BEIJING
WOS记录号WOS:000597401000021
内容类型期刊论文
源URL[http://ir.qdio.ac.cn/handle/337002/169399]  
专题海洋研究所_深海极端环境与生命过程研究中心
通讯作者Liu, Xi
作者单位1.China Univ Geosci Beijing, Sch Gemmol, Beijing 100083, Peoples R China
2.Chinese Acad Sci, Ctr Deep Sea Res, Inst Oceanog, Qingdao 266071, Peoples R China
3.Minist Educ China, Key Lab Orogen Belts & Crustal Evolut, Beijing 100871, Peoples R China
4.Chinese Acad Sci, Guangzhou Inst Geochem, Key Lab Mineral & Metallogeny, Guangzhou 510640, Peoples R China
5.Peking Univ, Sch Earth & Space Sci, Beijing 100871, Peoples R China
6.Univ Texas Austin, Jackson Sch Geosci, Dept Geol Sci, Austin, TX 78712 USA
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Yan, Wei,Zhang, Yanyao,Ma, Yunlu,et al. Water in coesite: Incorporation mechanism and operation condition, solubility and P-T dependence, and contribution to water transport and coesite preservation[J]. GEOSCIENCE FRONTIERS,2021,12(1):313-326.
APA Yan, Wei.,Zhang, Yanyao.,Ma, Yunlu.,He, Mingyue.,Zhang, Lifei.,...&Liu, Xi.(2021).Water in coesite: Incorporation mechanism and operation condition, solubility and P-T dependence, and contribution to water transport and coesite preservation.GEOSCIENCE FRONTIERS,12(1),313-326.
MLA Yan, Wei,et al."Water in coesite: Incorporation mechanism and operation condition, solubility and P-T dependence, and contribution to water transport and coesite preservation".GEOSCIENCE FRONTIERS 12.1(2021):313-326.
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