坦桑尼亚西北部Karagwe-Ankolean带花岗岩及相关热液岩中电气石的稳定同位素组成

R.P. Taylor , J.R. Ikingura , A.E. Fallick , Yiming Huang , D.H. Watkinson
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引用次数: 0

摘要

电气石是坦桑尼亚西北部Karagwe-Ankolean带中元古代、过铝质、同—后构造花岗岩、镁铝岩及相关热液岩中普遍存在的矿物。电子探针分析表明,所有侵入岩和热液岩性中的电气石:(1)属榴辉岩固溶体系列;(2) FeAlMg分类图上贫锂花岗岩中电气石所占地块。岩浆碧玺的氧同位素组成范围为+12.2 ~ +11.6‰(SMOW),热液碧玺的氧同位素组成范围为+10.8 ~ +9.8‰。岩浆碧玺的氢同位素组成变化范围为- 79 ~ - 65‰(SMOW),热液碧玺的氢同位素组成变化范围为- 99 ~ - 84‰。测压法测得的含水量恒定在3.0-3.2 wt.%。在广泛的分组中,化学[特别是Fetot(Fetot + Mg比值)]和同位素组成都有系统的变化,这些变化与岩浆和热液条件的演化有关。火成岩分异[岩浆电气石中Fetot(Fetot + Mg比值)增大]产生了石英δ18O高、电气石δ18O低、ΔQTZ.-TOUR大的趋势。-值,反映了结晶温度的降低和残余熔体中Fetot(Fetot + Mg比)的增加。随着溶蚀的富b岩浆与泥质岩石的冷却和相互作用,热液电气石沉积,Fetot(Fetot + Mg)比值增大,δ18O和δD值逐渐降低。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Stable isotope compositions of tourmalines from granites and related hydrothermal rocks of the Karagwe-Ankolean belt, northwest Tanzania

Tourmaline is a ubiquitous mineral in the Mid-Proterozoic, peraluminous, syn- to post-tectonic granites and aplites and the related hydrothermal rocks of the Karagwe-Ankolean belt in northwest Tanzania. Electron microprobe analysis indicates that tourmalines from all of the intrusive and hydrothermal lithologies: (1) belong to the schorl-dravite solid-solution series; and (2) plot within the field occupied by tourmaline from Li-poor granitoids on the FeAlMg classification diagram. Oxygen isotope compositions range from +12.2 to +11.6‰ (SMOW) for magmatic tourmalines and from +10.8 to +9.8‰ for those of hydrothermal origin. Hydrogen isotope compositions vary from −79 to −65‰ (SMOW ) for magmatic tourmalines and from −99 to −84‰ for hydrothermal tourmalines. Water contents measured by manometry are constant at 3.0–3.2 wt.%. Within the broad grouping there arc systematic variations in both chemical [particularly Fetot(Fetot + Mg ratio)] and isotopic composition that relate to evolving magmatic and hydrothermal conditions. Igneous differentiation [increasing Fetot(Fetot + Mg ratio) in magmatic tourmaline] has produced trends with higher δ18O in quartz, lower δ18O in tourmaline, and larger ΔQTZ.-TOUR.-values, that reflect a combination of a reduction of crystallization temperature and an increase of Fetot(Fetot + Mg ratio) in the residual melt. Subsequent cooling and interaction of an exsolved, B-rich magmatic fluid with the pelitic country rocks, resulted in the deposition of hydrothermal tourmaline with increasing Fetot(Fetot + Mg ratio) ratios, and progressively lower δ18O and δD -values.

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