Magma redox and structural controls on iron isotope variations in Earth's mantle and crust

The heavy iron isotopic composition of Earth's crust relative to chondrites has been explained by vaporization during the Moon-forming impact, equilibrium partitioning between metal and silicate at core–mantle-boundary conditions, or partial melting and magma differentiation. The latter view is...

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Veröffentlicht in:Earth and planetary science letters 2014-07, Vol.398, p.127-140
Hauptverfasser: Dauphas, N., Roskosz, M., Alp, E.E., Neuville, D.R., Hu, M.Y., Sio, C.K., Tissot, F.L.H., Zhao, J., Tissandier, L., Médard, E., Cordier, C.
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container_title Earth and planetary science letters
container_volume 398
creator Dauphas, N.
Roskosz, M.
Alp, E.E.
Neuville, D.R.
Hu, M.Y.
Sio, C.K.
Tissot, F.L.H.
Zhao, J.
Tissandier, L.
Médard, E.
Cordier, C.
description The heavy iron isotopic composition of Earth's crust relative to chondrites has been explained by vaporization during the Moon-forming impact, equilibrium partitioning between metal and silicate at core–mantle-boundary conditions, or partial melting and magma differentiation. The latter view is supported by the observed difference in the iron isotopic compositions of MORBS and peridotites. However, the precise controls on iron isotope variations in igneous rocks remain unknown. Here, we show that equilibrium iron isotope fractionation is mainly controlled by redox (Fe3+/Fetot ratio) and structural (e.g., polymerization) conditions in magmas. We measured, for the first time, the mean force constants of iron bonds in silicate glasses by synchrotron Nuclear Resonant Inelastic X-ray Scattering (NRIXS, also known as Nuclear Resonance Vibrational Spectroscopy – NRVS, or Nuclear Inelastic Scattering – NIS). The same samples were studied by conventional Mössbauer and X-ray Absorption Near Edge Structure (XANES) spectroscopy. The NRIXS results reveal a +0.2 to +0.4‰ equilibrium fractionation on 56Fe/54Fe ratio between Fe2+ and Fe3+ end-members in basalt, andesite, and dacite glasses at magmatic temperatures. These first measurements can already explain ∼1/3 of the iron isotopic shift measured in MORBs relative to their source. Further work will be required to investigate how pressure, temperature, and structural differences between melts and glasses affect equilibrium fractionation factors. In addition, large fractionation is also found between rhyolitic glass and commonly occurring oxide and silicate minerals. This fractionation reflects mainly changes in the coordination environment of Fe2+ in rhyolites relative to less silicic magmas and mantle minerals, as also seen by XANES. We provide a new calibration of XANES features vs. Fe3+/Fetot ratio determinations by Mössbauer to estimate Fe3+/Fetot ratio in situ in glasses of basaltic, andesitic, dacitic, and rhyolitic compositions. Modeling of magma differentiation using rhyolite-MELTS shows that iron structural changes in silicic magmas can explain the heavy iron isotopic compositions of granitoids and rhyolites. This study demonstrates that iron stable isotopes can help reveal planetary redox conditions and igneous processes. Other heterovalent elements such as Ti, V, Eu, Cr, Ce, or U may show similar isotopic variations in bulk rocks and individual minerals, which could be used to establish past and present redox
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These first measurements can already explain ∼1/3 of the iron isotopic shift measured in MORBs relative to their source. Further work will be required to investigate how pressure, temperature, and structural differences between melts and glasses affect equilibrium fractionation factors. In addition, large fractionation is also found between rhyolitic glass and commonly occurring oxide and silicate minerals. This fractionation reflects mainly changes in the coordination environment of Fe2+ in rhyolites relative to less silicic magmas and mantle minerals, as also seen by XANES. We provide a new calibration of XANES features vs. Fe3+/Fetot ratio determinations by Mössbauer to estimate Fe3+/Fetot ratio in situ in glasses of basaltic, andesitic, dacitic, and rhyolitic compositions. Modeling of magma differentiation using rhyolite-MELTS shows that iron structural changes in silicic magmas can explain the heavy iron isotopic compositions of granitoids and rhyolites. 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The latter view is supported by the observed difference in the iron isotopic compositions of MORBS and peridotites. However, the precise controls on iron isotope variations in igneous rocks remain unknown. Here, we show that equilibrium iron isotope fractionation is mainly controlled by redox (Fe3+/Fetot ratio) and structural (e.g., polymerization) conditions in magmas. We measured, for the first time, the mean force constants of iron bonds in silicate glasses by synchrotron Nuclear Resonant Inelastic X-ray Scattering (NRIXS, also known as Nuclear Resonance Vibrational Spectroscopy – NRVS, or Nuclear Inelastic Scattering – NIS). The same samples were studied by conventional Mössbauer and X-ray Absorption Near Edge Structure (XANES) spectroscopy. The NRIXS results reveal a +0.2 to +0.4‰ equilibrium fractionation on 56Fe/54Fe ratio between Fe2+ and Fe3+ end-members in basalt, andesite, and dacite glasses at magmatic temperatures. These first measurements can already explain ∼1/3 of the iron isotopic shift measured in MORBs relative to their source. Further work will be required to investigate how pressure, temperature, and structural differences between melts and glasses affect equilibrium fractionation factors. In addition, large fractionation is also found between rhyolitic glass and commonly occurring oxide and silicate minerals. This fractionation reflects mainly changes in the coordination environment of Fe2+ in rhyolites relative to less silicic magmas and mantle minerals, as also seen by XANES. We provide a new calibration of XANES features vs. Fe3+/Fetot ratio determinations by Mössbauer to estimate Fe3+/Fetot ratio in situ in glasses of basaltic, andesitic, dacitic, and rhyolitic compositions. Modeling of magma differentiation using rhyolite-MELTS shows that iron structural changes in silicic magmas can explain the heavy iron isotopic compositions of granitoids and rhyolites. This study demonstrates that iron stable isotopes can help reveal planetary redox conditions and igneous processes. Other heterovalent elements such as Ti, V, Eu, Cr, Ce, or U may show similar isotopic variations in bulk rocks and individual minerals, which could be used to establish past and present redox condition in the mantles of Earth and other planets. •Fe force constants are measured in silicate glasses and olivine by synchrotron NRIXS.•Fe3+ has heavy isotopic composition relative to Fe2+ at magmatic temperatures.•The force constant of Fe2+ in rhyolite is higher than in less silicic magmas.•These results explain some of the Fe isotopic variations measured in igneous rocks.•A calibration is provided for determination of Fe3+/Fetot by XANES in glasses.</abstract><pub>Elsevier B.V</pub><doi>10.1016/j.epsl.2014.04.033</doi><tpages>14</tpages><orcidid>https://orcid.org/0000-0002-1330-2038</orcidid><orcidid>https://orcid.org/0000-0001-7503-8116</orcidid><orcidid>https://orcid.org/0000-0002-7040-7442</orcidid><orcidid>https://orcid.org/0000-0002-8487-5001</orcidid><oa>free_for_read</oa></addata></record>
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ispartof Earth and planetary science letters, 2014-07, Vol.398, p.127-140
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1385-013X
language eng
recordid cdi_hal_primary_oai_HAL_hal_01130702v1
source Elsevier ScienceDirect Journals
subjects Earth Sciences
Fractionation
Glass
Iron
Iron isotopes
isotopes
Magma
Minerals
NRIXS
Petrography
redox
Rhyolite
Sciences of the Universe
Silicates
XANES
title Magma redox and structural controls on iron isotope variations in Earth's mantle and crust
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