TY - JOUR
T1 - Melting of carbonated pelites at 2.5-5.0 GPa, silicate-carbonatite liquid immiscibility, and potassium-carbon metasomatism of the mantle
AU - Thomsen, Tonny B.
AU - Schmidt, Max W.
N1 - Funding Information:
This work is part of the PhD project of T.B. Thomsen, ETH grant TH 38/02-1. We are thankful to J.A.D. Connolly, P. Ulmer, and M. Caddick for discussions improving the manuscript. Thanks to E. Reusser, R. Rüthi, B. Kuhn, and L. Caricchi for assistance in the microprobe, to K. Kunze for SEM work, to S. Villiger, R. Kessel, P. Ardia, A. Hack, and M. Aerts for technical support in the laboratory, to P. Nievergelt, A. Stewart, and G. Solferino for solving computer problems, and to U. Graber and A. Jallas for mechanical support, and to Signe for all her support and patience. Constructive reviews by J. Hermann and an anonymous reviewer improved the final version of the manuscript.
PY - 2008/3/1
Y1 - 2008/3/1
N2 - Melting experiments on a Fe-rich carbonate-saturated pelite were performed at 850-1300 °C and 2.5-5.0 GPa to define melting relations, melt compositions, and the conditions under which carbonates remain residual. In the selected fertile bulk composition, 30 wt.% potassic granite (2.5 GPa) or phonolite (5.0 GPa) melt is generated at the fluid-absent solidus. The temperature of the latter increases from 900 °C at 2.4 GPa to 1070 °C at 5.0 GPa. Phengite + quartz/coesite control initial silicate melting and melt productivity through the reaction phengite + quartz/coesite +clinopyroxene + calcite = silicate melt + kyanite + garnet, which leaves most of the Fe-Mg-calcite in the residue. Na remains compatible in clinopyroxene (DNacpx/melt = 3.1 to 7.3 at the fluid-absent solidus), resulting in silicate melts with K2O/Na2O wt-ratios of 5.8-8.6. Such highly potassic carbonated silicate melts represent ideal metasomatic agents for the source mantle of group II kimberlites. From 3.7 to 5.0 GPa, Fe-Mg-calcite disappears only through the formation of Ca-carbonatite at 1100 °C. The experiments provide a possible source for Ca-carbonatites in combination with alkaline granitic to phonolitic melts at temperatures unlikely to be achieved during ongoing subduction. Large scale carbonate transfer to the subarc mantle can thus only be achieved when burying rates slow considerably down or subducted crust becomes incorporated into the mantle. Consequently, it is likely that carbonates will not be extensively mobilized in a typical subarc region, thus extending and confirming earlier results from subsolidus studies (Connolly, J.A.D., 2005. Computation of phase equilibria by linear programming: a tool for geodynamic modelling and its application to subduction zone decarbonation. Earth Planet. Sci. Lett. 236, 524-541.), that > 70-80% of the subducted carbonate will bypass the volcanic arc region and get buried to larger depths.
AB - Melting experiments on a Fe-rich carbonate-saturated pelite were performed at 850-1300 °C and 2.5-5.0 GPa to define melting relations, melt compositions, and the conditions under which carbonates remain residual. In the selected fertile bulk composition, 30 wt.% potassic granite (2.5 GPa) or phonolite (5.0 GPa) melt is generated at the fluid-absent solidus. The temperature of the latter increases from 900 °C at 2.4 GPa to 1070 °C at 5.0 GPa. Phengite + quartz/coesite control initial silicate melting and melt productivity through the reaction phengite + quartz/coesite +clinopyroxene + calcite = silicate melt + kyanite + garnet, which leaves most of the Fe-Mg-calcite in the residue. Na remains compatible in clinopyroxene (DNacpx/melt = 3.1 to 7.3 at the fluid-absent solidus), resulting in silicate melts with K2O/Na2O wt-ratios of 5.8-8.6. Such highly potassic carbonated silicate melts represent ideal metasomatic agents for the source mantle of group II kimberlites. From 3.7 to 5.0 GPa, Fe-Mg-calcite disappears only through the formation of Ca-carbonatite at 1100 °C. The experiments provide a possible source for Ca-carbonatites in combination with alkaline granitic to phonolitic melts at temperatures unlikely to be achieved during ongoing subduction. Large scale carbonate transfer to the subarc mantle can thus only be achieved when burying rates slow considerably down or subducted crust becomes incorporated into the mantle. Consequently, it is likely that carbonates will not be extensively mobilized in a typical subarc region, thus extending and confirming earlier results from subsolidus studies (Connolly, J.A.D., 2005. Computation of phase equilibria by linear programming: a tool for geodynamic modelling and its application to subduction zone decarbonation. Earth Planet. Sci. Lett. 236, 524-541.), that > 70-80% of the subducted carbonate will bypass the volcanic arc region and get buried to larger depths.
KW - carbonate-saturated pelite
KW - immiscible carbonatite
KW - KNCFMASH-CO
KW - melting experiments
KW - phengite
KW - silicate liquids
KW - Electron microprobe
KW - Experimental Petrology
KW - Marl
UR - http://www.scopus.com/inward/record.url?scp=39549090648&partnerID=8YFLogxK
U2 - 10.1016/j.epsl.2007.11.027
DO - 10.1016/j.epsl.2007.11.027
M3 - Article
AN - SCOPUS:39549090648
SN - 0012-821X
VL - 267
SP - 17
EP - 31
JO - Earth and Planetary Science Letters
JF - Earth and Planetary Science Letters
IS - 1-2
ER -