More Like this

1. Cation diffusion in magmatic olivine and the ‘melt problem’

   https://doi.org/10.46427/gold2022.12385  

   Shea, Tom; Ruth, Dawn (January 2022, European Association of Geochemistry)
2. Quantifying and correcting the effects of anisotropy in XANES measurements of chromium valence in olivine: Implications for a new olivine oxybarometer

   https://doi.org/10.2138/am-2017-5911  

   Bell, Aaron S.; Shearer, Charles; Burger, Paul; Ren, Minghua; Newville, Matthew; Lanzirotti, Antonio (June 2017, American Mineralogist)
3. Phosphorus Coupling Obfuscates Lithium Geospeedometry in Olivine

   https://doi.org/10.3389/feart.2020.00135  

   Lynn, Kendra J.; Garcia, Michael O.; Shea, Thomas (May 2020, Frontiers in Earth Science)
4. Trace element partitioning between olivine and melt in lunar basalts

   https://doi.org/10.2138/am-2022-7971  

   Chen, Sha; Ni, Peng; Zhang, Youxue; Gagnon, Joel (August 2022, American Mineralogist)

   Abstract Mineral/melt partition coefficients have been widely used to provide insights into magmatic processes. Olivine is one of the most abundant and important minerals in the lunar mantle and mare basalts. Yet, no systematic olivine/melt partitioning data are available for lunar conditions. We report trace element partition data between host mineral olivine and its melt inclusions in lunar basalts. Equilibrium is evaluated using the Fe-Mg exchange coefficient, leading to the choice of melt inclusion-host olivine pairs in lunar basalts 12040, 12009, 15016, 15647, and 74235. Partition coefficients of 21 elements (Li, Mg, Al, Ca, Ti, V, Cr, Mn, Fe, Co, Y, Zr, Nb, Gd, Tb, Dy, Ho, Er, Tm, Yb, and Lu) were measured. Except for Li, V, and Cr, these elements show no significant difference in olivine-melt partitioning compared to the data for terrestrial samples. The partition coefficient of Li between olivine and melt in some lunar basalts with low Mg# (Mg# < 0.75 in olivine, or < ~0.5 in melt) is higher than published data for terrestrial samples, which is attributed to the dependence of DLi on Mg# and the lack of literature DLi data with low Mg#. The partition coefficient of V in lunar basalts is measured to be 0.17 to 0.74, significantly higher than that in terrestrial basalts (0.003 to 0.21), which can be explained by the lower oxygen fugacity in lunar basalts. The significantly higher DV can explain why V is less enriched in evolved lunar basalts than terrestrial basalts. The partition coefficient of Cr between olivine and basalt melt in the Moon is 0.11 to 0.62, which is lower than those in terrestrial settings by a factor of ~2. This is surprising because previous authors showed that Cr partition coefficient is independent of fO2. A quasi-thermodynamically based model is developed to correlate Cr partition coefficient to olivine and melt composition and fO2. The lower Cr partition coefficient between olivine and basalt in the Moon can lead to more Cr enrichment in the lunar magma ocean, as well as more Cr enrichment in mantle-derived basalts in the Moon. Hence, even though Cr is typically a compatible element in terrestrial basalts, it is moderately incompatible in primitive lunar basalts, with a similar degree of incompatibility as V based on partition coefficients in this work, as also evidenced by the relatively constant V/Cr ratio of 0.039 ± 0.011 in lunar basalts. The confirmation of constant V/Cr ratio is important for constraining concentrations of Cr (slightly volatile and siderophile) and V (slightly siderophile) in the bulk silicate Moon. 

   more » « less
5. Abiotic methane synthesis and serpentinization in olivine-hosted fluid inclusions

   https://doi.org/10.1073/pnas.1907871116  

   Klein, Frieder; Grozeva, Niya G.; Seewald, Jeffrey S. (September 2019, Proceedings of the National Academy of Sciences)

   The conditions of methane (CH 4 ) formation in olivine-hosted secondary fluid inclusions and their prevalence in peridotite and gabbroic rocks from a wide range of geological settings were assessed using confocal Raman spectroscopy, optical and scanning electron microscopy, electron microprobe analysis, and thermodynamic modeling. Detailed examination of 160 samples from ultraslow- to fast-spreading midocean ridges, subduction zones, and ophiolites revealed that hydrogen (H 2 ) and CH 4 formation linked to serpentinization within olivine-hosted secondary fluid inclusions is a widespread process. Fluid inclusion contents are dominated by serpentine, brucite, and magnetite, as well as CH 4( g ) and H 2( g ) in varying proportions, consistent with serpentinization under strongly reducing, closed-system conditions. Thermodynamic constraints indicate that aqueous fluids entering the upper mantle or lower oceanic crust are trapped in olivine as secondary fluid inclusions at temperatures higher than ∼400 °C. When temperatures decrease below ∼340 °C, serpentinization of olivine lining the walls of the fluid inclusions leads to a near-quantitative consumption of trapped liquid H 2 O. The generation of molecular H 2 through precipitation of Fe(III)-rich daughter minerals results in conditions that are conducive to the reduction of inorganic carbon and the formation of CH 4 . Once formed, CH 4( g ) and H 2( g ) can be stored over geological timescales until extracted by dissolution or fracturing of the olivine host. Fluid inclusions represent a widespread and significant source of abiotic CH 4 and H 2 in submarine and subaerial vent systems on Earth, and possibly elsewhere in the solar system. 

   more » « less