Clinoeulite (magnesian clinoferrosilite) in a eulysite of a metamorphosed iron formation in the vredefort structure, South Africa
Clinoeulite (magnesian clinoferrosilite) in a eulysite of a metamorphosed iron formation in the vredefort structure, South Africa
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南非 vredefort 构造中变质铁岩层中的斜钙石(镁斜铁硅石)
DOI:
10.1007/bf00372283
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发表时间:
1978
影响因子:
3.5
通讯作者:
W. Müller
中科院分区:
文献类型:
--
作者:
W. Schreyer;D. Stepto;K. Abraham;W. Müller
AbstractA unique clinopyroxene (En19Fs78Wo3), clinoeulite, space group P21/c,
$${\text{(Fe}}_{{\text{1}}{\text{.48}}} {\text{Mg}}_{{\text{0}}{\text{.37}}} {\text{Mn}}_{{\text{0}}{\text{.08}}}^{{\text{2 + }}} {\text{Ca}}_{{\text{0}}{\text{.05}}} {\text{Al}}_{{\text{0}}{\text{.01}}} {\text{)}}_{{\text{1}}{\text{.99}}} {\text{ [Si}}_{{\text{2}}{\text{.01}}} {\text{O6],}}$$
contains sharp exsolution lamellae of ferroaugite (En17Fs43Wo40) from which the former presence of a ferropigeonite near En17Fs70Wo13 can be calculated. This two-pyroxene intergrowth is the main component of a eulysite containing also magnetite, olivine (Fo9Fa86Te5), quartz, oligoclase-K feldspar inter-growth, and retrograde cummingtonite with about 76 % grunerite end member.The occurrence of this most unusual rock type in the center of the Vredefort structure is attributed to a period of high-temperature metamorphism (at least 800 °–850 °C) which was followed by hot deformation of the rock during the Vredefort event thus probably preventing the common formation of orthopyroxene through pigeonite exsolution and inversion upon cooling. After this tectonic deformation, the rock recrystallized within the low-temperature stability range of clinoeulite to yield fine annealing textures. Late-stage equilibria at temperatures well below 500 °C include the complete unmixing of a former high-temperature anorthoclase, a Mg/Fe redistribution in the clinoeulite and olivine and, with the introduction of water, the partial formation of cummingtonite through reaction of clinoeulite, olivine, and quartz. During weathering the olivine was transformed to a nearly opaque, anhydrous ferrisilicate which, except for the change of Fe2+ to Fe3+ and the oxygen introduction, largely retained its original chemistry.