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Effect of water on carbonate-silicate liquid immiscibility in the system KAlSi3O8CaMgSi2O6-NaAlSi2O6-CaMg(CO3)2 at 6 GPa : Implications for diamond-forming melts. / Shatskiy, Anton; Arefiev, Anton V.; Podborodnikov, Ivan V. et al.

In: American Mineralogist, Vol. 106, No. 2, 23.02.2021, p. 165-173.

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Shatskiy A, Arefiev AV, Podborodnikov IV, Litasov KD. Effect of water on carbonate-silicate liquid immiscibility in the system KAlSi3O8CaMgSi2O6-NaAlSi2O6-CaMg(CO3)2 at 6 GPa: Implications for diamond-forming melts. American Mineralogist. 2021 Feb 23;106(2):165-173. doi: 10.2138/am-2020-7551

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Shatskiy, Anton ; Arefiev, Anton V. ; Podborodnikov, Ivan V. et al. / Effect of water on carbonate-silicate liquid immiscibility in the system KAlSi3O8CaMgSi2O6-NaAlSi2O6-CaMg(CO3)2 at 6 GPa : Implications for diamond-forming melts. In: American Mineralogist. 2021 ; Vol. 106, No. 2. pp. 165-173.

BibTeX

@article{758b55ba181d4135a6737078eec7514c,
title = "Effect of water on carbonate-silicate liquid immiscibility in the system KAlSi3O8CaMgSi2O6-NaAlSi2O6-CaMg(CO3)2 at 6 GPa: Implications for diamond-forming melts",
abstract = "To clarify the effect of water on carbonate-silicate liquid immiscibility in the diamond stability field, we performed experiments in the system KAlSi3O8-CaMgSi2O6-NaAlSi2O6-CaMg(CO3)2 under nominally dry and hydrous conditions by adding 1.5 wt% H2O at a pressure of 6 GPa and temperatures of 1000 to 1500 °C. Both systems start to melt at 1050–1100 °C. Under anhydrous condition the melting occurs via the following reaction: 6KAlSi3O8 (K-feldspar) + 6CaMg(CO3)2 (dolomite) = 2(Can,Mg1-n)3Al2Si3O12 (garnet) + Al2SiO5 (kyanite) + 11SiO2 (coesite) + 3 K2(Ca1-n, Mgn)2(CO3)3 (carbonatitic melt) + 3CO2 (fluid and/or liquid), where n ~ 0.3–0.4. The carbonatitic melt has the following composition 38(K0.92Na0.08)2CO362Ca0.62Mg0.38CO3. A second immiscible silicic melt containing (in wt%, volatile free) SiO2 = 68.8, Al2O3 = 12.6, CaO = 3.7, MgO = 2.4, Na2O = 1.1, and K2O = 11.3 appears at 1250 °C. Both melts remain stable up to 1500 °C and coexist with the clinopyroxene ± garnet ± coesite residue. In the presence of water stored away in phengite, the melting begins with silicic melt, which contains (in wt%, volatile free) SiO2 = 61.4, Al2O3 = 15.3, CaO = 4.8, MgO = 3.0, Na2O = 2.2, and K2O = 13.3, and coexists with phengite, dolomite, clinopyroxene, and coesite. The phengite + dolomite assemblage remains to 1100 °C and disappears at 1200 °C producing two immiscible melts carbonatitic with approximate composition, 19(K0.89Na0.11)2CO381Ca0.57Mg0.43CO3, and silicic containing (in wt%, volatile free) SiO2 = 63.3, Al2O3 = 15.6, CaO = 4.5, MgO = 3.0, Na2O = 2.0, K2O = 11.6. The present results imply that partial melting of continental material subducted to a depth of 200 km can yield simultaneous formation of two immiscible melts, K-dolomitic and K-aluminosilicate. Under dry conditions, carbonatitic melt appears earlier (at a lower temperature). Given the low density and high mobility of this melt, it must rapidly percolate upward, leaving a refractory eclogite-like residue and leaving no chance for the formation of a second aluminosilicate melt. However, under hydrous conditions silicate melt appears earlier than carbonatitic melt, leaving a phengite- and dolomite-bearing residue, which finally yields the formation of two immiscible silicic and carbonatitic melts. The compositions of these melts fall in the compositional range of carbonatitic and silicic high-density fluids (HDFs) in diamonds worldwide. Thus, we suggest that the presence of water is a necessary requirement for the formation of immiscible HDFs inclusions in diamonds, and this suggestion is strongly supported by natural data from HDFs.",
keywords = "Carbonate-silicate liquid immiscibility, Carbonated pelites, Diamond formation, Earth{\textquoteright}s upper mantle; New Advances in Subduction Zone Magma Genesis, High-density fluids, High-pressure experiment, K-feldspar, Phengite",
author = "Anton Shatskiy and Arefiev, {Anton V.} and Podborodnikov, {Ivan V.} and Litasov, {Konstantin D.}",
note = "Funding Information: We are grateful to N.S. Karmanov and A.T. Titov for their help in the analytical works. This study was done on the state assignment of IGM SB RAS. A.S. was supported by RFBR No. 20-05-00811. A.V.A. was supported by RFBR No. 19–35-90082. K.D.L. was supported by the state assignment of IHPP RAS. The SEM and EDX studies of experimental samples were performed in the Analytical Center for multi-elemental and isotope research SB RAS. Publisher Copyright: {\textcopyright} 2021 De Gruyter. All rights reserved. Copyright: Copyright 2021 Elsevier B.V., All rights reserved.",
year = "2021",
month = feb,
day = "23",
doi = "10.2138/am-2020-7551",
language = "English",
volume = "106",
pages = "165--173",
journal = "American Mineralogist",
issn = "0003-004X",
publisher = "Walter de Gruyter GmbH",
number = "2",

}

RIS

TY - JOUR

T1 - Effect of water on carbonate-silicate liquid immiscibility in the system KAlSi3O8CaMgSi2O6-NaAlSi2O6-CaMg(CO3)2 at 6 GPa

T2 - Implications for diamond-forming melts

AU - Shatskiy, Anton

AU - Arefiev, Anton V.

AU - Podborodnikov, Ivan V.

AU - Litasov, Konstantin D.

N1 - Funding Information: We are grateful to N.S. Karmanov and A.T. Titov for their help in the analytical works. This study was done on the state assignment of IGM SB RAS. A.S. was supported by RFBR No. 20-05-00811. A.V.A. was supported by RFBR No. 19–35-90082. K.D.L. was supported by the state assignment of IHPP RAS. The SEM and EDX studies of experimental samples were performed in the Analytical Center for multi-elemental and isotope research SB RAS. Publisher Copyright: © 2021 De Gruyter. All rights reserved. Copyright: Copyright 2021 Elsevier B.V., All rights reserved.

PY - 2021/2/23

Y1 - 2021/2/23

N2 - To clarify the effect of water on carbonate-silicate liquid immiscibility in the diamond stability field, we performed experiments in the system KAlSi3O8-CaMgSi2O6-NaAlSi2O6-CaMg(CO3)2 under nominally dry and hydrous conditions by adding 1.5 wt% H2O at a pressure of 6 GPa and temperatures of 1000 to 1500 °C. Both systems start to melt at 1050–1100 °C. Under anhydrous condition the melting occurs via the following reaction: 6KAlSi3O8 (K-feldspar) + 6CaMg(CO3)2 (dolomite) = 2(Can,Mg1-n)3Al2Si3O12 (garnet) + Al2SiO5 (kyanite) + 11SiO2 (coesite) + 3 K2(Ca1-n, Mgn)2(CO3)3 (carbonatitic melt) + 3CO2 (fluid and/or liquid), where n ~ 0.3–0.4. The carbonatitic melt has the following composition 38(K0.92Na0.08)2CO362Ca0.62Mg0.38CO3. A second immiscible silicic melt containing (in wt%, volatile free) SiO2 = 68.8, Al2O3 = 12.6, CaO = 3.7, MgO = 2.4, Na2O = 1.1, and K2O = 11.3 appears at 1250 °C. Both melts remain stable up to 1500 °C and coexist with the clinopyroxene ± garnet ± coesite residue. In the presence of water stored away in phengite, the melting begins with silicic melt, which contains (in wt%, volatile free) SiO2 = 61.4, Al2O3 = 15.3, CaO = 4.8, MgO = 3.0, Na2O = 2.2, and K2O = 13.3, and coexists with phengite, dolomite, clinopyroxene, and coesite. The phengite + dolomite assemblage remains to 1100 °C and disappears at 1200 °C producing two immiscible melts carbonatitic with approximate composition, 19(K0.89Na0.11)2CO381Ca0.57Mg0.43CO3, and silicic containing (in wt%, volatile free) SiO2 = 63.3, Al2O3 = 15.6, CaO = 4.5, MgO = 3.0, Na2O = 2.0, K2O = 11.6. The present results imply that partial melting of continental material subducted to a depth of 200 km can yield simultaneous formation of two immiscible melts, K-dolomitic and K-aluminosilicate. Under dry conditions, carbonatitic melt appears earlier (at a lower temperature). Given the low density and high mobility of this melt, it must rapidly percolate upward, leaving a refractory eclogite-like residue and leaving no chance for the formation of a second aluminosilicate melt. However, under hydrous conditions silicate melt appears earlier than carbonatitic melt, leaving a phengite- and dolomite-bearing residue, which finally yields the formation of two immiscible silicic and carbonatitic melts. The compositions of these melts fall in the compositional range of carbonatitic and silicic high-density fluids (HDFs) in diamonds worldwide. Thus, we suggest that the presence of water is a necessary requirement for the formation of immiscible HDFs inclusions in diamonds, and this suggestion is strongly supported by natural data from HDFs.

AB - To clarify the effect of water on carbonate-silicate liquid immiscibility in the diamond stability field, we performed experiments in the system KAlSi3O8-CaMgSi2O6-NaAlSi2O6-CaMg(CO3)2 under nominally dry and hydrous conditions by adding 1.5 wt% H2O at a pressure of 6 GPa and temperatures of 1000 to 1500 °C. Both systems start to melt at 1050–1100 °C. Under anhydrous condition the melting occurs via the following reaction: 6KAlSi3O8 (K-feldspar) + 6CaMg(CO3)2 (dolomite) = 2(Can,Mg1-n)3Al2Si3O12 (garnet) + Al2SiO5 (kyanite) + 11SiO2 (coesite) + 3 K2(Ca1-n, Mgn)2(CO3)3 (carbonatitic melt) + 3CO2 (fluid and/or liquid), where n ~ 0.3–0.4. The carbonatitic melt has the following composition 38(K0.92Na0.08)2CO362Ca0.62Mg0.38CO3. A second immiscible silicic melt containing (in wt%, volatile free) SiO2 = 68.8, Al2O3 = 12.6, CaO = 3.7, MgO = 2.4, Na2O = 1.1, and K2O = 11.3 appears at 1250 °C. Both melts remain stable up to 1500 °C and coexist with the clinopyroxene ± garnet ± coesite residue. In the presence of water stored away in phengite, the melting begins with silicic melt, which contains (in wt%, volatile free) SiO2 = 61.4, Al2O3 = 15.3, CaO = 4.8, MgO = 3.0, Na2O = 2.2, and K2O = 13.3, and coexists with phengite, dolomite, clinopyroxene, and coesite. The phengite + dolomite assemblage remains to 1100 °C and disappears at 1200 °C producing two immiscible melts carbonatitic with approximate composition, 19(K0.89Na0.11)2CO381Ca0.57Mg0.43CO3, and silicic containing (in wt%, volatile free) SiO2 = 63.3, Al2O3 = 15.6, CaO = 4.5, MgO = 3.0, Na2O = 2.0, K2O = 11.6. The present results imply that partial melting of continental material subducted to a depth of 200 km can yield simultaneous formation of two immiscible melts, K-dolomitic and K-aluminosilicate. Under dry conditions, carbonatitic melt appears earlier (at a lower temperature). Given the low density and high mobility of this melt, it must rapidly percolate upward, leaving a refractory eclogite-like residue and leaving no chance for the formation of a second aluminosilicate melt. However, under hydrous conditions silicate melt appears earlier than carbonatitic melt, leaving a phengite- and dolomite-bearing residue, which finally yields the formation of two immiscible silicic and carbonatitic melts. The compositions of these melts fall in the compositional range of carbonatitic and silicic high-density fluids (HDFs) in diamonds worldwide. Thus, we suggest that the presence of water is a necessary requirement for the formation of immiscible HDFs inclusions in diamonds, and this suggestion is strongly supported by natural data from HDFs.

KW - Carbonate-silicate liquid immiscibility

KW - Carbonated pelites

KW - Diamond formation

KW - Earth’s upper mantle; New Advances in Subduction Zone Magma Genesis

KW - High-density fluids

KW - High-pressure experiment

KW - K-feldspar

KW - Phengite

UR - http://www.scopus.com/inward/record.url?scp=85089550981&partnerID=8YFLogxK

U2 - 10.2138/am-2020-7551

DO - 10.2138/am-2020-7551

M3 - Article

AN - SCOPUS:85089550981

VL - 106

SP - 165

EP - 173

JO - American Mineralogist

JF - American Mineralogist

SN - 0003-004X

IS - 2

ER -

ID: 27708299