TY - JOUR
T1 - Iron isotopic fractionation in mineral phases from Earth's lower mantle
T2 - Did terrestrial magma ocean crystallization fractionate iron isotopes?
AU - Yang, Hong
AU - Lin, Jung Fu
AU - Hu, Michael Y.
AU - Roskosz, Mathieu
AU - Bi, Wenli
AU - Zhao, Jiyong
AU - Alp, Esen E.
AU - Liu, Jin
AU - Liu, Jiachao
AU - Wentzowitch, Renata M.
AU - Okuchi, Takuo
AU - Dauphas, Nicolas
N1 - Funding Information:
We thank J. Yang, S. Fu, C. Zhang, N. Purevjav, T. Inoue, and S. Jacobsen for experimental assistance, T. Qin for helpful discussions, and F. O'toole for editing the manuscript. J.F. Lin acknowledges support from the U.S. National Science Foundation Geophysics and CSEDI Programs as well as the Center for High Pressure Science and Technology Advanced Research (HPSTAR). HPSTAR is supported by NSAF (Grant No. U1530402 ). N. Dauphas acknowledges support from National Science Foundation (Cooperative Studies of the Earth's Deep Interior, EAR150259 ; Petrology and Geochemistry, EAR144495 ) and NASA (Laboratory Analysis of Returned Samples, NNX14AK09G ; Cosmochemistry, OJ-30381-0036A and NNX15AJ25G ). M. Roskosz acknowledges support from the French ANR ( 2011JS5600401 , FrIHIDDA). W. Bi acknowledges the support from the Consortium for Materials Properties Research in Earth Sciences (COMPRES), the National Science Foundation (NSF) through Grant No. DMR-1104742 . We acknowledge GSECARS and HPCAT of the APS for use of their diffraction and ruby facilities. This research used resources of the Advanced Photon Source, a U.S. Department of Energy (DOE) Office of Science User Facility operated for the DOE Office of Science by Argonne National Laboratory under Contract No. DE-AC02-06CH11357.
Funding Information:
We thank J. Yang, S. Fu, C. Zhang, N. Purevjav, T. Inoue, and S. Jacobsen for experimental assistance, T. Qin for helpful discussions, and F. O'toole for editing the manuscript. J.F. Lin acknowledges support from the U.S. National Science Foundation Geophysics and CSEDI Programs as well as the Center for High Pressure Science and Technology Advanced Research (HPSTAR). HPSTAR is supported by NSAF (Grant No. U1530402). N. Dauphas acknowledges support from National Science Foundation (Cooperative Studies of the Earth's Deep Interior, EAR150259; Petrology and Geochemistry, EAR144495) and NASA (Laboratory Analysis of Returned Samples, NNX14AK09G; Cosmochemistry, OJ-30381-0036A and NNX15AJ25G). M. Roskosz acknowledges support from the French ANR (2011JS5600401, FrIHIDDA). W. Bi acknowledges the support from the Consortium for Materials Properties Research in Earth Sciences (COMPRES), the National Science Foundation (NSF) through Grant No. DMR-1104742. We acknowledge GSECARS and HPCAT of the APS for use of their diffraction and ruby facilities. This research used resources of the Advanced Photon Source, a U.S. Department of Energy (DOE) Office of Science User Facility operated for the DOE Office of Science by Argonne National Laboratory under Contract No. DE-AC02-06CH11357.
Publisher Copyright:
© 2018 Elsevier B.V.
PY - 2019/1/15
Y1 - 2019/1/15
N2 - Iron is the most abundant transition metal in the Earth's interior, yet considerable uncertainties remain as to why mantle-derived rocks have diverse iron isotopic compositions. In particular, the isotopic fractionation behavior of iron in the lower-mantle minerals bridgmanite and ferropericlase are largely unexplored. The reason is that it is challenging to study isotopic fractionation at the high pressures relevant to the deep mantle. Here we report in situ measurements of the mean force constants of iron bonds in these minerals pressurized in diamond anvil cells using the technique of nuclear resonant inelastic X-ray scattering (NRIXS). We find that the transition from high- to low-spin iron in ferropericlase ((Mg0.75Fe0.25)O) at approximately 60 GPa drastically stiffens its iron bonds in the low-spin state. The mean force constant of iron bonds in both Fe-bearing and (Fe,Al)-bearing bridgmanite exhibits softening by 21% at approximately 40–60 GPa, which seems to be associated with changes in the iron local environment during the transition from low to high quadrupole splitting states. These results indicate that in the lower mantle, low-spin ferropericlase is enriched in heavy iron isotopes relative to bridgmanite and metallic iron by +0.15‰ and +0.12‰ respectively. Based on these results, we investigate whether terrestrial magma ocean crystallization could have fractionated iron isotopes. We conclude that this process cannot be responsible for the heavy iron isotope enrichment measured in terrestrial basalts.
AB - Iron is the most abundant transition metal in the Earth's interior, yet considerable uncertainties remain as to why mantle-derived rocks have diverse iron isotopic compositions. In particular, the isotopic fractionation behavior of iron in the lower-mantle minerals bridgmanite and ferropericlase are largely unexplored. The reason is that it is challenging to study isotopic fractionation at the high pressures relevant to the deep mantle. Here we report in situ measurements of the mean force constants of iron bonds in these minerals pressurized in diamond anvil cells using the technique of nuclear resonant inelastic X-ray scattering (NRIXS). We find that the transition from high- to low-spin iron in ferropericlase ((Mg0.75Fe0.25)O) at approximately 60 GPa drastically stiffens its iron bonds in the low-spin state. The mean force constant of iron bonds in both Fe-bearing and (Fe,Al)-bearing bridgmanite exhibits softening by 21% at approximately 40–60 GPa, which seems to be associated with changes in the iron local environment during the transition from low to high quadrupole splitting states. These results indicate that in the lower mantle, low-spin ferropericlase is enriched in heavy iron isotopes relative to bridgmanite and metallic iron by +0.15‰ and +0.12‰ respectively. Based on these results, we investigate whether terrestrial magma ocean crystallization could have fractionated iron isotopes. We conclude that this process cannot be responsible for the heavy iron isotope enrichment measured in terrestrial basalts.
KW - iron isotopic fractionation
KW - magma ocean crystallization
KW - nuclear resonant spectroscopy
KW - spin transition
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U2 - 10.1016/j.epsl.2018.10.034
DO - 10.1016/j.epsl.2018.10.034
M3 - Article
AN - SCOPUS:85056234033
SN - 0012-821X
VL - 506
SP - 113
EP - 122
JO - Earth and Planetary Science Letters
JF - Earth and Planetary Science Letters
ER -