TY - JOUR
T1 - Solidus of carbonated peridotite from 10 to 20 GPa and origin of magnesiocarbonatite melt in the Earth's deep mantle
AU - Ghosh, Sujoy
AU - Ohtani, Eiji
AU - Litasov, Konstantin D.
AU - Terasaki, Hidenori
N1 - Funding Information:
We thank Rajdeep Dasgupta for inviting us to contribute in this special volume. We are grateful to R. Dasgupta, S Keshav, M. Nakamura and A. Suzuki for useful discussions. We also acknowledge constructive reviews by two anonymous reviewers. We thank M. Miyahara, Y. Ito and S. Ozawa for their technical assistance with scanning electron microscope, electron probe and Raman spectroscopy analyses. S.G. gratefully acknowledges the Ministry of Education, Culture, Science, Sport and Technology, Japan for providing him the Monbukagakusho Fellowship. This work was supported by the Grants-in-aid for Scientific Research from Ministry of Education, Culture, Science, Sport and Technology of Japanese Government (No. 15104009 and 16075202) to E. O., and conducted as a part of the 21st Century-of-Excellence program, ‘Advanced Science and Technology Center for the Dynamic Earth’ at Tohoku University.
PY - 2009/5
Y1 - 2009/5
N2 - We have experimentally determined the solidus of an alkali-bearing carbonated peridotite (with 5 wt.% CO2) between 10 and 20 GPa. Based on K-deficit in all low-temperature runs we assumed that some melt could be present in the low temperature runs and the true solidus of an alkali-bearing carbonated peridotite is placed below 1200 °C. However, based on the disappearance of magnesite and the appearance of the visible quenched melt coexisting with silicate phases, the 'apparent' solidus, which may be applicable for peridotite with low alkali contents, was identified. The 'apparent' solidus temperature increases from ~1380 °C at 10 GPa to ~1525 °C at 15 GPa and the 'apparent' solidus curve becomes almost flat from 15 GPa to 20 GPa, where it is located near 1550 °C. At 10 GPa, the 'apparent' solidus of carbonated peridotite is ~550 °C lower than the solidus of CO2-free natural anhydrous peridotite. The solidus of the present study was also ~120 °C lower than the solidus determined by Dasgupta and Hirschmann [Dasgupta, R., Hirschmann, M.M., 2006. Melting in the Earth's deep upper mantle caused by carbon dioxide. Nature, 440, 659-662.] for natural carbonated peridotite. The drop in the solidus temperature is mainly due to the effect of alkalis (Na2O, K2O). The melt near the 'apparent' solidus has high CO2 (>40 wt.%) and contains b6.0 wt.% SiO2, <0.30 wt.% Al2O3 and <0.25 wt.% TiO2. The composition of near-solidus partial melt is close to that observed at 6-10 GPa in the CMS-CO2 and CMAS-CO2 systems, and natural carbonated peridotite, with some variations in Ca/Mg-ratio. High alkali contents in measured and calculated partial melts are consistent with the compositions of deepseated fluids observed as inclusions in diamonds and may be consistent with the compositions of parental melt, reconstructed for natural magnesiocarbonatite. We have demonstrated that magnesiocarbonatite-like melt can be generated by partial melting of carbonated peridotite at pressure up to at least 20 GPa. The generation of calciocarbonatite and ferrocarbonatite is unlikely to be possible during melting of carbonated peridotite in the deep mantle.
AB - We have experimentally determined the solidus of an alkali-bearing carbonated peridotite (with 5 wt.% CO2) between 10 and 20 GPa. Based on K-deficit in all low-temperature runs we assumed that some melt could be present in the low temperature runs and the true solidus of an alkali-bearing carbonated peridotite is placed below 1200 °C. However, based on the disappearance of magnesite and the appearance of the visible quenched melt coexisting with silicate phases, the 'apparent' solidus, which may be applicable for peridotite with low alkali contents, was identified. The 'apparent' solidus temperature increases from ~1380 °C at 10 GPa to ~1525 °C at 15 GPa and the 'apparent' solidus curve becomes almost flat from 15 GPa to 20 GPa, where it is located near 1550 °C. At 10 GPa, the 'apparent' solidus of carbonated peridotite is ~550 °C lower than the solidus of CO2-free natural anhydrous peridotite. The solidus of the present study was also ~120 °C lower than the solidus determined by Dasgupta and Hirschmann [Dasgupta, R., Hirschmann, M.M., 2006. Melting in the Earth's deep upper mantle caused by carbon dioxide. Nature, 440, 659-662.] for natural carbonated peridotite. The drop in the solidus temperature is mainly due to the effect of alkalis (Na2O, K2O). The melt near the 'apparent' solidus has high CO2 (>40 wt.%) and contains b6.0 wt.% SiO2, <0.30 wt.% Al2O3 and <0.25 wt.% TiO2. The composition of near-solidus partial melt is close to that observed at 6-10 GPa in the CMS-CO2 and CMAS-CO2 systems, and natural carbonated peridotite, with some variations in Ca/Mg-ratio. High alkali contents in measured and calculated partial melts are consistent with the compositions of deepseated fluids observed as inclusions in diamonds and may be consistent with the compositions of parental melt, reconstructed for natural magnesiocarbonatite. We have demonstrated that magnesiocarbonatite-like melt can be generated by partial melting of carbonated peridotite at pressure up to at least 20 GPa. The generation of calciocarbonatite and ferrocarbonatite is unlikely to be possible during melting of carbonated peridotite in the deep mantle.
KW - Carbonated peridotite
KW - Carbonatite
KW - Geotherm
KW - Mantle
KW - Solidus
KW - Transition zone
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U2 - 10.1016/j.chemgeo.2008.12.030
DO - 10.1016/j.chemgeo.2008.12.030
M3 - Article
AN - SCOPUS:67650216205
SN - 0009-2541
VL - 262
SP - 17
EP - 28
JO - Chemical Geology
JF - Chemical Geology
IS - 1-2
ER -