High-pressure partial melting of mafic lithologies in the mantle

被引:231
|
作者
Kogiso, T
Hirschmann, MM
Pertermann, M
机构
[1] Japan Agcy Marine Earth Sci & Technol, IFREE, Yokosuka, Kanagawa 2370061, Japan
[2] Univ Minnesota, Dept Geol & Geophys, Minneapolis, MN 55455 USA
[3] ETH, Inst Mineral & Petrog, CH-8902 Zurich, Switzerland
基金
美国国家科学基金会;
关键词
experimental petrology; mantle heterogeneity; partial melting; phase equilibrium; pyroxenite;
D O I
10.1093/petrology/egh057
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
We review experimental phase equilibria associated with partial melting of mafic lithologies (pyroxenites) at high pressures to reveal systematic relationships between bulk compositions of pyroxenite and their melting relations. An important aspect of pyroxenite phase equilibria is the existence of the garnet-pyroxene thermal divide, defined by the enstatite-Ca-Tschermaks pyroxene-diopside plane in CaO-MgO-Al2O3-SiO2 projections. This divide appears at pressures above similar to2 GPa in the natural system where garnet and pyroxenes are the principal residual phases in pyroxenites. Bulk compositions that reside on either side of the divide have distinct phase assemblages from subsolidus to liquidus and produce distinct types of partial melt ranging from strongly nepheline-normative to quartz-normative compositions. Solidus and liquidus locations are little affected by the location of natural pyroxenite compositions relative to the thermal divide and are instead controlled chiefly by bulk alkali contents and Mg-numbers. Changes in phase volumes of residual minerals also influence partial melt compositions. If olivine is absent during partial melting, expansion of the phase volume of garnet relative to clinopyroxene with increasing pressure produces liquids with high Ca/Al and low MgO compared with garnet peridotite-derived partial melts.
引用
收藏
页码:2407 / 2422
页数:16
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