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American Mineralogist; September 1999; v. 84; no. 9; p. 1304-1318
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Hydrothermal synthesis of amphiboles along the tremolite-pargasite join and in the ternary system tremolite-pargasite-cummingtonite

Anurag Sharma, and David M. Jenkins

Carnegie Institute of Washington, Geophysical Laboratory, Washington, DC, United States
Binghamton University, United States

We report here an investigation of amphibole synthesis within the ternary system Ca 2 Mg 5 Si 8 O 22 (OH) 2 -NaCa 2 Mg 4 Al 3 Si 6 O 22 (OH) 2 -Mg 7 Si (sub 8 ) O 22 (OH) 2 (= TR-PG-MC) to define better the limits of solid solution for amphiboles formed along and near the join tremolite-pargasite. Hydrothermal syntheses were conducted in the range of 750-1000 degrees C and 1-6 kbar. Syntheses at 10 mol% compositional intervals along the TR-PG join produced incomplete yields of amphibole, and the resultant amphiboles were found to be associated with varying amounts of accessory clinopyroxene, plagioclase, and gehlenite. Syntheses of end-member pargasite with progressively greater amounts of the MC component produced a very good amphibole yield for a pargasite composition containing 2.5 mol% MC. The persistence of clinopyroxene or gehlenite and the improved yield of pargasitic amphibole with minor addition of the MC component indicate a shift toward MC enrichment for amphiboles made from bulk compositions directly on the TR-PG join. Syntheses within the TR-PG-MC ternary system suggest that the Ca-rich limit of solid solution is a slightly curved field in the TR-PG-MC field. Amphiboles made along this join showed a very systematic change in the (151) and (331) peak spacing with mol% PG, providing a simple technique for deducing the composition of amphiboles made near the tremolite-pargasite join. Electron microprobe analysis confirms that the amphiboles for the most part conform to the "pargasite" substitution. The one exception being amphiboles formed near 80-90 mol% PG compositions, which proved both difficult to synthesize ( approximately 75 wt% amphibole yield) and displayed a small, but significant, excess of Na in their structure. High yields of amphibole could be formed from this same bulk composition with the use of a dilute NaOH solution instead of pure water, suggesting that there was insufficient Na in the starting mixture to allow complete amphibole formation. Structural refinements using X-ray diffraction (XRD) Rietveld refinement confirmed the high Na content for this sample and also revealed a non-linear trend in the unit-cell volume with composition, with a maximum at the 80 mol% PG bulk composition. The difficulty in synthesizing amphiboles near this bulk composition and its unusually high volume suggest that immiscibility in natural hornblendes may initiate with increasing pressure for pargasite-rich bulk compositions.

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