The calcite→aragonite transformation in low-Mg marble:: Equilibrium relations, transformation mechanisms, and rates -: art. no. B03205

被引:28
作者
Hacker, BR [1 ]
Rubie, DC
Kirby, SH
Bohlen, SR
机构
[1] Univ Calif Santa Barbara, Dept Geol Sci, Santa Barbara, CA 93106 USA
[2] Joint Oceanog Inst, Washington, DC 20192 USA
[3] Univ Bayreuth, Bayer Geo Inst, D-95490 Bayreuth, Germany
[4] US Geol Survey, Menlo Pk, CA 94025 USA
关键词
D O I
10.1029/2004JB003302
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
Experimental transformation of a rather pure natural calcite marble to aragonite marble did not proceed via the expected straightforward polymorphic replacement. Instead, the small amount of Mg in the starting material (0.36 wt%) was excluded from the growing aragonite and diffused preferentially into the remaining calcite grains, producing Mg-rich calcite rods that persisted as relicts. Nucleation of aragonite occurred exclusively on grain boundaries, with aragonite [001] oriented subparallel to calcite [0001]. The aragonite crystals preferentially consumed the calcite crystal on which they nucleated, and the reaction fronts developed preferentially along the {010} and {110} planes of aragonite. Each aragonite neoblast that grew was nearly free of Mg (typically < 0.1 wt%). The excess Mg was taken up by the calcite grains in between, stabilizing them and causing a few volume percent rodlike relicts of Mg- enriched calcite (up to 10 wt% MgO) to be left behind by the advancing reaction front. The aragonite growth rates are approximately linear and range from similar to 3 x 10(-11) m s(-1) at 600 degrees C to similar to 9 x 10(-9) m s(-1) at 850 degrees C, with an apparent activation enthalpy of 166 +/- 91 kJ mol(-1). This reaction mechanism and the resultant texture are akin to cellular precipitation reactions in metals. Similar transformation textures have been reported from high-Mg marbles in Japan and China that disproportionated to low-Mg calcite and dolomite.
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页码:1 / 16
页数:16
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