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Phase relations on the K2CO3-CaCO3-MgCO3 join at 6 GPa and 900-1400 °C : Implications for incipient melting in carbonated mantle domains. / Shatskiy, Anton; Litasov, Konstantin D.; Palyanov, Yuri N. et al.

In: American Mineralogist, Vol. 101, No. 2, 01.01.2016, p. 437-447.

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@article{1b78ec52627d489b8c2a24578a5711d1,
title = "Phase relations on the K2CO3-CaCO3-MgCO3 join at 6 GPa and 900-1400 °C: Implications for incipient melting in carbonated mantle domains",
abstract = "To constrain the ternary K2CO3-CaCO3-MgCO3 T-X diagram at 6 GPa and to expand upon the known K-Mg, K-Ca, and Ca-Mg binary systems we have carried out multi-anvil experiments along the K2CO3-Ca0.5Mg0.5CO3 join. The diagram has primary phase fields for K2CO3, K2Mg(CO3)2, K2Ca0.1-0.5 Mg0.9-0.5(CO3)2, K4CaMg(CO3)4, Ca-magnesite, and dolomite. The system has two liquidus minima near 1000 °C. At one minimum, a liquid with the composition of 36 K2CO3·64(Ca0.65Mg0.35)CO3 is in equilibrium with three phases: Ca-magnesite, K2Ca0.1-0.5Mg0.9-0.5(CO3)2, and K6Ca2(CO3)5. The other minimum, a liquid with the composition of 62 K2CO3·38Ca0.72Mg0.28CO3 is in equilibrium with K2CO3, K4CaMg(CO3)4, and K6Ca2(CO3)5. At 900 °C, the ternary diagram contains two- and three-phase regions with Ca-magnesite, aragonite, K2Ca3(CO3)4, K2Ca(CO3)2, K6Ca2(CO3)5, K2CO3, K2Ca0.1-0.5Mg0.9-0.5(CO3)2 solid solution, K2Mg0.9Ca0.1(CO3)2, and K4CaMg(CO3)4. We also expect an existence of primary phase fields for K6Ca2(CO3)5, K2Ca3(CO3)4 and aragonite. We suggest that extraction of K from silicate to carbonate components should decrease the minimum melting temperature of dry carbonated mantle rocks up to 1000 °C at 6 GPa and yield ultrapotassic Ca-rich dolomite melt containing more than 10 mol% K2CO3. As temperature increases above 1200 °C the melt evolves toward an alkali-poor, dolomitic liquid if the bulk molar CaO/MgO ratio >1, or toward K-Mg-rich carbonatite if bulk CaO/MgO <1. The majority of compositions of carbonatite inclusions in diamonds from around the world fall within the magnesite primary field between the 1300 and 1400 °C isotherms. These melts could be formed by partial melting of magnesite-bearing peridotite or eclogite with bulk Ca/Mg <1 at temperatures ≤1400 °C. A few compositions revealed in the Ebelyakh and Udachnaya diamonds (Yakutia) fall within the dolomite primary field close to the 1200 °C isotherm. These melts could be formed by partial melting of dolomite-bearing rocks, such as carbonated pelite or eclogite with bulk Ca/Mg <1 at temperatures ≤1200 °C.",
keywords = "Deep earth, high pressure, high temperature, melts, phase relations",
author = "Anton Shatskiy and Litasov, {Konstantin D.} and Palyanov, {Yuri N.} and Eiji Ohtani",
year = "2016",
month = jan,
day = "1",
doi = "10.2138/am-2016-5332",
language = "English",
volume = "101",
pages = "437--447",
journal = "American Mineralogist",
issn = "0003-004X",
publisher = "Walter de Gruyter GmbH",
number = "2",

}

RIS

TY - JOUR

T1 - Phase relations on the K2CO3-CaCO3-MgCO3 join at 6 GPa and 900-1400 °C

T2 - Implications for incipient melting in carbonated mantle domains

AU - Shatskiy, Anton

AU - Litasov, Konstantin D.

AU - Palyanov, Yuri N.

AU - Ohtani, Eiji

PY - 2016/1/1

Y1 - 2016/1/1

N2 - To constrain the ternary K2CO3-CaCO3-MgCO3 T-X diagram at 6 GPa and to expand upon the known K-Mg, K-Ca, and Ca-Mg binary systems we have carried out multi-anvil experiments along the K2CO3-Ca0.5Mg0.5CO3 join. The diagram has primary phase fields for K2CO3, K2Mg(CO3)2, K2Ca0.1-0.5 Mg0.9-0.5(CO3)2, K4CaMg(CO3)4, Ca-magnesite, and dolomite. The system has two liquidus minima near 1000 °C. At one minimum, a liquid with the composition of 36 K2CO3·64(Ca0.65Mg0.35)CO3 is in equilibrium with three phases: Ca-magnesite, K2Ca0.1-0.5Mg0.9-0.5(CO3)2, and K6Ca2(CO3)5. The other minimum, a liquid with the composition of 62 K2CO3·38Ca0.72Mg0.28CO3 is in equilibrium with K2CO3, K4CaMg(CO3)4, and K6Ca2(CO3)5. At 900 °C, the ternary diagram contains two- and three-phase regions with Ca-magnesite, aragonite, K2Ca3(CO3)4, K2Ca(CO3)2, K6Ca2(CO3)5, K2CO3, K2Ca0.1-0.5Mg0.9-0.5(CO3)2 solid solution, K2Mg0.9Ca0.1(CO3)2, and K4CaMg(CO3)4. We also expect an existence of primary phase fields for K6Ca2(CO3)5, K2Ca3(CO3)4 and aragonite. We suggest that extraction of K from silicate to carbonate components should decrease the minimum melting temperature of dry carbonated mantle rocks up to 1000 °C at 6 GPa and yield ultrapotassic Ca-rich dolomite melt containing more than 10 mol% K2CO3. As temperature increases above 1200 °C the melt evolves toward an alkali-poor, dolomitic liquid if the bulk molar CaO/MgO ratio >1, or toward K-Mg-rich carbonatite if bulk CaO/MgO <1. The majority of compositions of carbonatite inclusions in diamonds from around the world fall within the magnesite primary field between the 1300 and 1400 °C isotherms. These melts could be formed by partial melting of magnesite-bearing peridotite or eclogite with bulk Ca/Mg <1 at temperatures ≤1400 °C. A few compositions revealed in the Ebelyakh and Udachnaya diamonds (Yakutia) fall within the dolomite primary field close to the 1200 °C isotherm. These melts could be formed by partial melting of dolomite-bearing rocks, such as carbonated pelite or eclogite with bulk Ca/Mg <1 at temperatures ≤1200 °C.

AB - To constrain the ternary K2CO3-CaCO3-MgCO3 T-X diagram at 6 GPa and to expand upon the known K-Mg, K-Ca, and Ca-Mg binary systems we have carried out multi-anvil experiments along the K2CO3-Ca0.5Mg0.5CO3 join. The diagram has primary phase fields for K2CO3, K2Mg(CO3)2, K2Ca0.1-0.5 Mg0.9-0.5(CO3)2, K4CaMg(CO3)4, Ca-magnesite, and dolomite. The system has two liquidus minima near 1000 °C. At one minimum, a liquid with the composition of 36 K2CO3·64(Ca0.65Mg0.35)CO3 is in equilibrium with three phases: Ca-magnesite, K2Ca0.1-0.5Mg0.9-0.5(CO3)2, and K6Ca2(CO3)5. The other minimum, a liquid with the composition of 62 K2CO3·38Ca0.72Mg0.28CO3 is in equilibrium with K2CO3, K4CaMg(CO3)4, and K6Ca2(CO3)5. At 900 °C, the ternary diagram contains two- and three-phase regions with Ca-magnesite, aragonite, K2Ca3(CO3)4, K2Ca(CO3)2, K6Ca2(CO3)5, K2CO3, K2Ca0.1-0.5Mg0.9-0.5(CO3)2 solid solution, K2Mg0.9Ca0.1(CO3)2, and K4CaMg(CO3)4. We also expect an existence of primary phase fields for K6Ca2(CO3)5, K2Ca3(CO3)4 and aragonite. We suggest that extraction of K from silicate to carbonate components should decrease the minimum melting temperature of dry carbonated mantle rocks up to 1000 °C at 6 GPa and yield ultrapotassic Ca-rich dolomite melt containing more than 10 mol% K2CO3. As temperature increases above 1200 °C the melt evolves toward an alkali-poor, dolomitic liquid if the bulk molar CaO/MgO ratio >1, or toward K-Mg-rich carbonatite if bulk CaO/MgO <1. The majority of compositions of carbonatite inclusions in diamonds from around the world fall within the magnesite primary field between the 1300 and 1400 °C isotherms. These melts could be formed by partial melting of magnesite-bearing peridotite or eclogite with bulk Ca/Mg <1 at temperatures ≤1400 °C. A few compositions revealed in the Ebelyakh and Udachnaya diamonds (Yakutia) fall within the dolomite primary field close to the 1200 °C isotherm. These melts could be formed by partial melting of dolomite-bearing rocks, such as carbonated pelite or eclogite with bulk Ca/Mg <1 at temperatures ≤1200 °C.

KW - Deep earth

KW - high pressure

KW - high temperature

KW - melts

KW - phase relations

UR - http://www.scopus.com/inward/record.url?scp=84959170673&partnerID=8YFLogxK

U2 - 10.2138/am-2016-5332

DO - 10.2138/am-2016-5332

M3 - Article

AN - SCOPUS:84959170673

VL - 101

SP - 437

EP - 447

JO - American Mineralogist

JF - American Mineralogist

SN - 0003-004X

IS - 2

ER -

ID: 25725456