Mineral/melt partitioning of trace elements during hydrous peridotite partial melting |
| |
Authors: | Glenn?A.?Gaetani author-information" > author-information__contact u-icon-before" > mailto:ggaetani@whoi.edu" title=" ggaetani@whoi.edu" itemprop=" email" data-track=" click" data-track-action=" Email author" data-track-label=" " >Email author,Adam?J.?R.?Kent,Timothy?L.?Grove,Ian?D.?Hutcheon,Edward?M.?Stolper |
| |
Affiliation: | (1) Department of Earth, Atmospheric and Planetary Sciences, Massachusetts Institute of Technology, Cambridge, MA, 02139, USA;(2) Division of Geological and Planetary Sciences, California Institute of Technology, Pasadena, CA, 91125, USA;(3) Department of Geology and Geophysics, Woods Hole Oceanographic Institution, Woods Hole, MA, 02543, USA;(4) Analytical and Nuclear Chemistry Division, Lawrence Livermore National Laboratory, Livermore, CA, 94551, USA;(5) Present address: Department of Geosciences, Oregon State University, Corvallis, OR, 97331-5506, USA |
| |
Abstract: | This experimental study examines the mineral/melt partitioning of incompatible trace elements among high-Ca clinopyroxene, garnet, and hydrous silicate melt at upper mantle pressure and temperature conditions. Experiments were performed at pressures of 1.2 and 1.6 GPa and temperatures of 1,185 to 1,370 °C. Experimentally produced silicate melts contain up to 6.3 wt% dissolved H 2O, and are saturated with an upper mantle peridotite mineral assemblage of olivine+orthopyroxene+clinopyroxene+spinel or garnet. Clinopyroxene/melt and garnet/melt partition coefficients were measured for Li, B, K, Sr, Y, Zr, Nb, and select rare earth elements by secondary ion mass spectrometry. A comparison of our experimental results for trivalent cations (REEs and Y) with the results from calculations carried out using the Wood-Blundy partitioning model indicates that H 2O dissolved in the silicate melt has a discernible effect on trace element partitioning. Experiments carried out at 1.2 GPa, 1,315 °C and 1.6 GPa, 1,370 °C produced clinopyroxene containing 15.0 and 13.9 wt% CaO, respectively, coexisting with silicate melts containing ~1–2 wt% H 2O. Partition coefficients measured in these experiments are consistent with the Wood-Blundy model. However, partition coefficients determined in an experiment carried out at 1.2 GPa and 1,185 °C, which produced clinopyroxene containing 19.3 wt% CaO coexisting with a high-H 2O (6.26±0.10 wt%) silicate melt, are significantly smaller than predicted by the Wood-Blundy model. Accounting for the depolymerized structure of the H 2O-rich melt eliminates the mismatch between experimental result and model prediction. Therefore, the increased Ca 2+ content of clinopyroxene at low-temperature, hydrous conditions does not enhance compatibility to the extent indicated by results from anhydrous experiments, and models used to predict mineral/melt partition coefficients during hydrous peridotite partial melting in the sub-arc mantle must take into account the effects of H 2O on the structure of silicate melts. |
| |
Keywords: | |
本文献已被 SpringerLink 等数据库收录! |
|