HR: 15:00h
AN: V42E-06 [PDF]
TI: Stability of Carbonated Eclogite in the Upper Mantle: Experimental Solidus from 2 to 9 GPa
AU: * Dasgupta, R
EM: dasg0007@umn.edu
AF: Department of Geology and Geophysics, University of Minnesota, 310 Pillsbury Dr SE, Minneapolis, MN
55455 United States
AU: Withers, A C
EM: withe012@umn.edu
AF: Department of Geology and Geophysics, University of Minnesota, 310 Pillsbury Dr SE, Minneapolis, MN
55455 United States
AU: Hirschmann, M M
EM: hirsc022@umn.edu
AF: Department of Geology and Geophysics, University of Minnesota, 310 Pillsbury Dr SE, Minneapolis, MN
55455 United States
AB:
Carbonates are pervasive alteration products of the oceanic crust and likely survive subduction-related dehydration and/or
melting. Thus, significant quantities of carbonated refractory eclogite are probably delivered to the deeper mantle. The
melting behavior of such recycled carbonate influences the fate of recycled carbon, determines the possible sources and
depths of carbonated metasomatic melts in the mantle, and delimits the conditions under which carbonated eclogite may act as
a source of carbonatite and other types of magmatic CO$_{2}$.
We present partial melting experiments of carbonated eclogite that constrain the solidus and near solidus phase relations
from 2 to 9 GPa. To simulate the near-isochemical nature of ocean floor carbonation, the starting material was prepared by
adding 5 wt.$%$ CO$_{2}$ in the form of a mixture of Fe-Mg-Ca-Na-K carbonates to a bimineralic eclogite from Salt Lake
crater, Oahu, Hawaii. The starting composition is a reasonable approximation of carbonated oceanic crust from which siliceous
hydrous fluid has been extracted by subduction. We find that melt-present versus melt-absent conditions can be
distinguished based on textural criteria. Garnet and cpx appear in all the experiments. Between 2 and 3 GPa, the subsolidus
assemblage also includes calcite-dolomite$_{ss}$ + ilmenite, whereas above the solidus (950-975 $\deg$C at 2 GPa and
1050-1075 $\deg$C at 3 GPa) calcio-dolomitic liquid appears. From 3 to 4.5 GPa, dolomite$_{ss}$ becomes stable at the solidus
and the near solidus melt becomes increasingly dolomitic. Appearance of dolomite above 3 GPa is accompanied by a negative
Clapeyron slope of the solidus, with the cusp located between 995 and 1025 $\deg$C at ${\it ca.}$ 4 GPa. Above 4-4.5 GPa, the
solidus again rises with increasing pressure to ${\it ca.}$ 1245 $\deg$C at 9 GPa and magnesite becomes the subsolidus
carbonate. Dolomitic melt coexists with magnesite + garnet + cpx + rutile between 5 and 9 GPa.
If extrapolated to higher pressures, the carbonated eclogite solidus intersects the oceanic geotherm deeper than 400 km.
Thus, eclogite cannot host carbonates in the asthenosphere. Carbonated eclogite bodies entering the convecting upper mantle
would release carbonate melt in the mantle transition zone. Upon release, this small volume, highly reactive melt could be
an effective agent of deep mantle metasomatism. Comparison of our eclogite-CO$_{2}$ solidus with that of peridotite-CO$_{2}$
shows a shallower solidus-geotherm intersection for the latter. This implies that carbonated peridotite is a more likely
proximal source of magmatic carbon in oceanic provinces. However, carbonated eclogite is a potential source of continental
carbonatites, as its solidus crosses the continental shield geotherm at ${\it ca.}$ 4 GPa.
DE: 1000 GEOCHEMISTRY (New field, replaces Rock Chemistry)
DE: 3630 Experimental mineralogy and petrology
DE: 3640 Igneous petrology
DE: 3655 Major element composition
DE: 4806 Carbon cycling
SC: Volcanology, Geochemistry, Petrology [V]
MN: 2003 Fall Meeting