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Water and fabric in an ophiolitic peridotite from a supra-subduction zone

机译:超俯冲带蛇纹岩橄榄岩中的水和织物

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Mantle peridotites from modern supra-subduction zones (SSZs) are important windows through which we can investigate the geodynamic processes active in the subduction factory, but they are unfortunately rare and hard to access. Most ophiolitic peridotites stem from SSZ settings and are therefore good candidates to explore the water budget and deformation in mantle wedges. We present here an integrated study of the geochemistry, deformation microstructures and water contents of olivine and orthopyroxene from the Dongqiao harzburgites, central Tibet. These peridotites are characterized by an absence of interstitial clinopyroxene, the partial replacement of orthopyroxene by olivine, the highly magnesian olivine and chromium spinel, and remarkable LREE enrichments. These features suggest that the Dongqiao harzburgites are highly depleted and have undergone a high degree (similar to 40 %) of partial melting, followed by infiltration of and interaction with melt while they were part of the mantle wedge. Olivine and orthopyroxene show prominent plastic deformation microstructures and have developed significant crystallographic preferred orientations (CPOs), suggestive of dislocation creep deformation. Fourier transform infrared analyses show that olivine is essentially dry, while orthopyroxene contains an average water content of 70 +/- 14 wt ppm. We propose that orthopyroxene largely retains its in-situ water content from the mantle source, while olivine completely loses its water during emplacement. The orthopyroxene water contents fall into the lower end of the range observed in SSZ peridotites. We consider that the high degree of partial melting and the interaction with a water-undersaturated melt contribute to the relatively lower water contents in orthopyroxene from the Dongqiao harzburgites. Based on experimentally determined hydrogen partition coefficients between olivine and orthopyroxene, the water contents of olivine in the mantle source are calculated to be 7-9 wt ppm (or 114-147 ppm H/Si), which is consistent with the observed A-type CPOs in olivine.
机译:来自现代超俯冲带(SSZs)的地幔橄榄岩是重要的窗口,通过它我们可以调查俯冲工厂中活跃的地球动力学过程,但不幸的是,它们很少见且难以接近。多数蛇纹岩橄榄岩都来自SSZ设置,因此是探索水的收支平衡和地幔楔形变形的理想人选。在这里,我们对西藏中部东桥哈兹伯格人的橄榄石和邻苯二酚的地球化学,变形微观结构和水含量进行了综合研究。这些橄榄岩的特征是不存在间质环吡rox烯,橄榄石部分取代邻苯二酚,高镁橄榄石和铬尖晶石以及显着的LREE富集。这些特征表明,东桥哈尔伯格岩高度贫化,并且经历了高度(大约40%)的部分熔融,随后在它们是地幔楔的一部分时渗透并与熔体相互作用。橄榄石和邻二甲苯显示出显着的塑性变形微观结构,并已发展出明显的晶体学优选取向(CPO),表明位错蠕变变形。傅里叶变换红外分析表明,橄榄石基本上是干燥的,而邻苯二甲酚的平均水含量为70 +/- 14 wt ppm。我们建议邻苯二甲醚在很大程度上保留了来自地幔源的原位水含量,而橄榄石在安置过程中完全失去了水分。邻苯二酚水含量降至SSZ橄榄岩中观察到的范围的下限。我们认为,部分熔融的高度程度以及与水饱和度较低的熔体之间的相互作用,导致了东桥哈兹伯格人邻苯二甲酚中相对较低的水分含量。根据实验确定的橄榄石和邻苯二甲hydrogen之间的氢分配系数,地幔源中橄榄石的水含量计算为7-9 wt ppm(或114-147 ppm H / Si),与观察到的A型一致橄榄石中的CPO。

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