4.7 Article

Titanium solubility in coexisting garnet and clinopyroxene at very high pressure: the significance of exsolved rutile in garnet

期刊

EARTH AND PLANETARY SCIENCE LETTERS
卷 216, 期 4, 页码 591-601

出版社

ELSEVIER
DOI: 10.1016/S0012-821X(03)00551-X

关键词

high-P experiment; Ti solubility; rutile exsolution; majorite; garnet clinopyroxenite

向作者/读者索取更多资源

Exsolution microstructures including ilmenite+/-garnet in clinopyroxene and rutile in garnet are common in clinopyroxenite and eclogite from the Sulu ultrahigh-pressure (UHP) terrane. In order to understand the phase relations and Ti solubility in both garnet and clinopyroxene in a natural TiO2-bearing system, several experiments at 5-15 GPa, 1000-1400degreesC were carried out using the multianvil high-pressure apparatus. The Hujianlin ilmenite-rich garnet clinopyroxenite showing exsolution microstructure was selected as starting material, because it closely approaches a composition lying in the TiO2-CaO-MgO-FeO-Al2O3-SiO2 system. Except for minor melt in one experiment at 1400degreesC and 5 GPa, other run products contain majoritic garnet+clinopyroxene+/-ilmenite (or rutile) and exhibit neoblastic texture. With increasing pressure, Ti and Ca, Mg and Si contents of neoblastic garnet increase with decreasing Al. The principal coupled substitutions are Ca2+Ti4+ --> 2Al(3+) and Si4+Mg2+ --> 2Al(3+) responding to majorite component increase. Titanium solubility (0.8-4.5 wt% as TiO2) in garnet and Grt(Ti)/Cpx(Ti) ratio have a pronounced positive correlation with pressure between 5 and 15 GPa. On the other hand, the coexisting clinopyroxene contains low Ti (0.17-0.53 wt% as TiO2), and shows no significant pressure effect. Rutile exsolution in garnet is coupled to that of pyroxene exsolution; both are exsolved from majoritic garnet on decompression. Therefore, the amount of such exsolved lamellae is a potential indicator of high-pressure metamorphism in exhumed rocks, whereas the TiO2 content of clinopyroxene coexisting with garnet is not sensitive to pressure change. (C) 2003 Elsevier B.V. All rights reserved.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据