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Paper No. 12
Presentation Time: 11:15 AM

CONTROLS ON CRYSTAL MORPHOLOGY, SIZE, NUMBER DENSITY, AND OXYGEN ISOTOPE COMPOSITION DURING FORMATION OF FORSTERITE BY SILICIFICATION OF DOLOMITE DURING CONTACT METAMORPHISM


FERRY, John M.1, USHIKUBO, Takayuki2, VALLEY, John W.2 and CURRIER, Ryan M.3, (1)Earth and Planetary Sciences, Johns Hopkins University, Baltimore, MD 21218, (2)Geoscience, University of Wisconsin, 1215 West Dayton Street, Madison, WI 53706, (3)Earth and Planetary Sciences, Johns Hopkins University, Olin Hall, 3400 N. Charles St, Baltimore, MD 21218, jferry@jhu.edu

Four samples that experienced the infiltration-driven reaction, 2 dolomite (Dol) + SiO2(aq) = forsterite (Fo) + 2 calcite (Cal) + 2 CO2, exhibit correlations among Fo crystal morphology, size, number density, and oxygen isotope ratio (δ18O). The δ18O of coexisting Fo, Cal, and Dol were determined by in situ ion microprobe analysis with a spatial resolution of ~15 μm. Sample KP1L from the Twin Lakes pendant, Sierra Nevada, California, contains blocky Fo with the largest average crystal size (190 μm) and the lowest number density (1.5·105 crystals/cm3 Fo). Fo and Cal are uniform in δ18O [δ18O(Fo) = 6.8±0.2 ‰, ±2 SE] with the measured fractionation [Δ18O(Cal-Fo) = 4.2±0.2 ‰] consistent with equilibrium at the temperature recorded by mineral equilibria (595 °C). Sample B4L from the Beinn an Dubhaich aureole, Scotland, contains tabular Fo with intermediate average size (47 μm) and number density (9.6·106 cm-3). Fo and Cal are uniform in δ18O [δ18O(Fo) = 18.8±0.2 ‰] but the measured fractionation [Δ18O(Cal-Fo) = 2.6±0.3 ‰] is smaller than the equilibrium value (3.6 ‰) at the temperature recorded by mineral equilibria (680 °C). Samples B1W and B43A from the Beinn an Dubhaich aureole contain rounded, bead-like Fo with the smallest average size (26-36 μm) and largest number density [(2-6)·107 cm-3]. Fo has variable δ18O (9.8-17.2 ‰), differing among grains by up to 7.4 ‰ in individual samples and by up to 3.1 ‰ within an individual grain, precluding isotope equilibrium with Cal and Dol. Crystal morphology, size, number density, δ18O(Fo), and Δ18O(Cal-Fo) can be understood in terms of the interplay between reaction affinity (A) and Peclet Number (Pe) during formation of Fo (KP1L: low A, high Pe; B4L: intermediate A and low Pe; B43A: high A, low Pe; B1W: high A, increasing Pe). Ranges in A and Pe are explained by variation in XCO2 of infiltrating fluid and in either fluid flux or width of the reaction zone, respectively. If infiltrating fluids are initially quartz-saturated, development of Fo (and periclase) from Dol during contact metamorphism must be preceded by reaction of fluid with Cal and Dol marble to produce diopside, wollastonite, and other skarn minerals, and thereby reduce aSiO2 to the low values required by phase equilibria.
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