Stable isotope geochemistry and phase equilibria whiteschists, Dora Maira Massif, western Alps
Z. D. Sharp, Eric J. Essene, J. C. Hunziker
Abstract
Z. D. Sharp, Eric J. Essene, J. C. Hunziker
Abstract
Peak metamorphic temperatures for the coesite-pyrope-bearing whiteschists from the Dora Maira Massif, western Alps were determined with oxygen iso- tope thermometry. The 818 O(svow) values of the quartz (after coesite) (~18 0 = 8.1 to 8.6%0, n = 6), phengite (6.2 to 6.4%o, n = 3), kyanite (6.1%o, n = 2), garnet (5.5 to 5.8%~ n = 9), ellenbergerite (6.3%0, n = 1) and futile (3.3. to 3.6%0, n = 3) reflect isotopic equilibrium. Temperature estimates based on quartz-garnet-ruffle fractionation are 700- 750 ~ Minimum pressures are 31-32 kb based on the pressure-sensitive reaction pyrope + coesite = kyanite + enstatite. In order to stabilize pyrope and coesite by the temperature-sensitive dehydration reaction talc + kyanite = pyrope + coesite + H20, the a(H20) must be reduced to 0.4-0.75 at 700-750 ~ The reduced a(H20) cannot be due to dilution by CO2, as pyrope is not stable at X(CO2) > 0.02 (T = 750 ~ P = 30 kb), In the absence of a more exotic fluid diluent (e.g. CH4 or N2), a melt phase is required. Granite solidus temperatures are ~680 ~ kb at a(HzO) = 1.0 and are calculated to be 70 ~ higher at a(H20) = 0.7, consistent with this hy- pothesis. Kyanite-jadeite-quartz bands may represent a relict melt phase. Peak P-T-f (H20) estimates for the whiteschist are 34 __+ 2 kb, 700-750 ~ and 0.4-0.75. The oxygen isotope fractionation between quartz (51sO = 11.6%o) and garnet (5180 = 8.7%0) in the sur- rounding orthognesiss is identical to that in the coesite- bearing unit, suggesting that the two units shared a com- mon, final metamorphic history. Hydrogen isotope measurements were made on primary talc and phengite (SD~s~ow~ = -27 to -32%o), on secondary talc and chlo- rite after pyrope (SD = -39 to -44%~ and on the sur- rounding biotite (SD = -64%o) and phengite (SD = -44%0) gneiss. All phases appear to be in near- equilibrium. The very high 8D values for the primary hydrous phases is consistent with an initial oceanic- derived/connate fluid source. The fluid source for the retrograde talc + chlorite after pyrope may be fluids evol- ved locally during retrograde melt crystallization. The similar 6D, but dissimilar 8180 values of the coesite- bearing whiteschists and hosting orthogneiss suggest that the two were in hydrogen isotope equilibrium, but not oxygen isotope equilibrium. The unusual hydrogen and oxygen isotope compositions of the coesite-bearing unit can be explained as the result of metasomatism from slab-derived fluids at depth.
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Peak metamorphic temperatures for the coesite-pyrope-bearing whiteschists from the Dora Maira Massif, western Alps were determined with oxygen iso- tope thermometry. The 818 O(svow) values of the quartz (after coesite) (~18 0 = 8.1 to 8.6%0, n = 6), phengite (6.2 to 6.4%o, n = 3), kyanite (6.1%o, n = 2), garnet (5.5 to 5.8%~ n = 9), ellenbergerite (6.3%0, n = 1) and futile (3.3. to 3.6%0, n = 3) reflect isotopic equilibrium. Temperature estimates based on quartz-garnet-ruffle fractionation are 700- 750 ~ Minimum pressures are 31-32 kb based on the pressure-sensitive reaction pyrope + coesite = kyanite + enstatite. In order to stabilize pyrope and coesite by the temperature-sensitive dehydration reaction talc + kyanite = pyrope + coesite + H20, the a(H20) must be reduced to 0.4-0.75 at 700-750 ~ The reduced a(H20) cannot be due to dilution by CO2, as pyrope is not stable at X(CO2) > 0.02 (T = 750 ~ P = 30 kb), In the absence of a more exotic fluid diluent (e.g. CH4 or N2), a melt phase is required. Granite solidus temperatures are ~680 ~ kb at a(HzO) = 1.0 and are calculated to be 70 ~ higher at a(H20) = 0.7, consistent with this hy- pothesis. Kyanite-jadeite-quartz bands may represent a relict melt phase. Peak P-T-f (H20) estimates for the whiteschist are 34 __+ 2 kb, 700-750 ~ and 0.4-0.75. The oxygen isotope fractionation between quartz (51sO = 11.6%o) and garnet (5180 = 8.7%0) in the sur- rounding orthognesiss is identical to that in the coesite- bearing unit, suggesting that the two units shared a com- mon, final metamorphic history. Hydrogen isotope measurements were made on primary talc and phengite (SD~s~ow~ = -27 to -32%o), on secondary talc and chlo- rite after pyrope (SD = -39 to -44%~ and on the sur- rounding biotite (SD = -64%o) and phengite (SD = -44%0) gneiss. All phases appear to be in near- equilibrium. The very high 8D values for the primary hydrous phases is consistent with an initial oceanic- derived/connate fluid source. The fluid source for the retrograde talc + chlorite after pyrope may be fluids evol- ved locally during retrograde melt crystallization. The similar 6D, but dissimilar 8180 values of the coesite- bearing whiteschists and hosting orthogneiss suggest that the two were in hydrogen isotope equilibrium, but not oxygen isotope equilibrium. The unusual hydrogen and oxygen isotope compositions of the coesite-bearing unit can be explained as the result of metasomatism from slab-derived fluids at depth.
Key concepts: Coesite, Pyrope, Kyanite, Geology, Massif, Mineralogy, Quartz, Geochemistry