HR: 0800h
AN: V31C-0607 [Abstracts]
TI: Lherzolite-saturated melt compositions of peridotite MM3: results of near-solidus micro- sandwich experiments
AU: * Baker, M B
EM: mikeb@gps.caltech.edu
AF: Division of Geological and Planetary Sciences, California Institute of Technology,
Pasadena, CA 91125, United States
AU: Stolper, E M
EM: ems@gps.caltech.edu
AF: Division of Geological and Planetary Sciences, California Institute of Technology,
Pasadena, CA 91125, United States
AB:
Results of the 1 GPa diamond-aggregate melting experiments of Baker and Stolper (1) and Baker et al. (2) on the
peridotite composition MM3 continue to be controversial (3,4), especially regarding the observation (1,2) of high
SiO2 and low TiO2 contents of partial melts produced near the solidus. Here we present the results of
four 1 GPa micro-sandwich experiments on MM3 at near-solidus temperatures of 1245-1250°C. As in our
earlier experiments (1,2), the MM3 mix consists of natural olivine, orthopyroxene, clinopyroxene, and spinel grains
that are less than 15 microns in size. Four different synthetic glass compositions were used and all lie off the
compositional trends defined by the MM3 partial melts in oxide vs. MgO space (1,2,5). Experimental charges were
constructed by placing a small chip of synthetic glass (0.4-0.8 mg) within a much larger mass (13-14 mg) of
powdered MM3; each combined glass-MM3 sample was run in a graphite crucible within a sealed Pt capsule for
122 to 144 hr in a piston cylinder apparatus. At P and T, the initial glass chip within a charge generates a small
pool of liquid whose composition shifts as it equilibrates with the MM3 solid phase assemblage. If the near-
solidus MM3 partial melting trend of (1,2,5) is correct, then experiments with different initial glass compositions
will produce final liquids that are consistent with this compositional trend. Except for TiO2 vs. MgO in one
experiment, the final glasses all lie within 1-2 sigma of the oxide vs. MgO trends defined by the partial melts of
MM3 (1,2,5). Note, that by minimizing the amount of basaltic glass added to MM3 in each experiment (mass
fractions varied from 0.03-0.06), the glasses do not substantially perturb the bulk composition of the starting
peridotite, which minimizes the need for iterative sandwich experiments (e.g., 6). We also compared the liquid
compositions from both the peridotite melting experiments and traditional sandwich experiments of (4; done
using a synthetic oxide mix of MM3) with our data (1,2,5). The two data sets overlap at the 1-2 sigma level when
liquid compositions are plotted as a function of liquid MgO content and thus, contrary to the claims of (4), the two
data sets are consistent with each other. The divergence of the two data sets when liquid compositions are
plotted as a function of temperature reflects the increasing concentration of K2O, P2O5,
H2O, and Cl in the partial melts of (1,2) compared to the liquids of (4), whose synthetic bulk compositions
were K2O, P2O5, and Cl-free. Results of our micro-sandwich experiments lend support to the
partial melting trend of (1,2,5) on MM3, especially with regard to the high SiO2 and low TiO2 contents in
liquids at low degrees of partial melting.
(1) Baker and Stolper (1994) GCA 58, 2811-2827; (2) Baker et al. (1995)
Nature 375, 308-311; (3) Falloon et al. (1997) EPSL 152, 149-162; (4) Falloon et al. (1999) JPet 40, 1343-1375;
(5) Hirschmann et al. GCA 62, 883-902; (6) Robinson et al. (1998) EPSL 155, 97-111
DE: 1065 Major and trace element geochemistry
DE: 3612 Reactions and phase equilibria (1012, 8412)
DE: 3619 Magma genesis and partial melting (1037)
DE: 3630 Experimental mineralogy and petrology
SC: Volcanology, Geochemistry, Petrology [V]
MN: 2007 Fall Meeting