Publishing type：Research paper (scientific journal)   Publisher：Japan Academy  

DOI： 10.2183/pjab.98.015

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Language：English   Publishing type：Research paper (scientific journal)   Publisher：WILEY  

Sample return missions represent great opportunities to study terrestrially uncontaminated solar system materials. However, the size of returned samples will be limited, and thus, it is necessary to understand the most appropriate techniques to apply. Accordingly, the sensitivity of laser ablation inductively coupled plasma mass spectrometry (LA-ICPMS) and secondary ion mass spectrometry (SIMS) was compared through the analyses of trace elements in reference materials and the Allende CV3 chondrite. While the SIMS method was found to be more sensitive than the laser method toward all elements of interest, the LA-ICPMS appears to be more suitable in terms of precision for certain elements. Using both analytical techniques, we measured chemical composition of an Allende chondrule and its igneous rim. These data were used to understand the nature of the reservoir that interacted with the host chondrule during formation of its igneous rim. We find that the igneous rim is enriched in silica, alkalis, and rare earth elements compared to the host chondrule. We suggest that the igneous rim could be explained by melting of a mixture of the chondrule-like and REE-enriched CAI-like precursors that accreted on the surface of the host chondrule followed by gas-melt interaction with a silica- and alkali-rich gas. Alternatively, these observations could be interpreted as a result of interaction between the chondrule and the melt resulting from partial melting of a pre-existing planetesimal in the early stages of its differentiation.

DOI： 10.1111/maps.13665

Web of Science

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Other Link： https://onlinelibrary.wiley.com/doi/full-xml/10.1111/maps.13665

Language：English   Publishing type：Research paper (scientific journal)   Publisher：WILEY  

Sample decomposition using inverse aqua regia at elevated temperatures and pressures (e.g., Carius tube or high-pressure asher) is the most common method used to extract highly siderophile elements (HSEs: Ru, Rh, Pd, Re, Os, Ir, Pt and Au) from geological samples. Recently, it has been recognised that additional HF desilicification is necessary to better recover HSEs, potentially contained within silicate or oxide minerals in mafic samples, which cannot be dissolved solely by inverse aqua regia. However, the abundance of interfering elements tends to increase in the eluent when conventional ion-exchange purification procedures are applied to desilicified samples. In this study, we developed an improved purification method to determine HSEs in desilicified samples. This method enables the reduction of the ratios of isobaric and polyatomic interferences, relative to the measured intensities of HSE isotope masses, to less than a few hundred parts per million. Furthermore, the total procedural blanks are either comparable to or lower than conventional methods. Thus, this method allows accurate and precise HSE measurements in mafic and ultramafic geological samples, without the need for interference corrections. Moreover, the problem of increased interfering elements, such as Zr for Pd and Cr for Ru, is circumvented for the desilicified samples.

DOI： 10.1111/ggr.12280

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Other Link： https://onlinelibrary.wiley.com/doi/full-xml/10.1111/ggr.12280

Language：English   Publishing type：Research paper (scientific journal)   Publisher：JAPAN ACAD  

A comprehensive geochemical study of the Chelyabinsk meteorite reveals further details regarding its history of impact-related fragmentation and melting, and later aqueous alteration, during its transit toward Earth. We support an similar to 30 Ma age obtained by Ar-Ar method (Beard et al., 2014) for the impact-related melting, based on Rb-Sr isotope analyses of a melt domain. An irregularly shaped olivine with a distinct 0 isotope composition in a melt domain appears to be a fragment of a silicate-rich impactor. Hydrogen and Li concentrations and isotopic compositions, textures of Fe oxyhydroxides, and the presence of organic materials located in fractures, are together consistent with aqueous alteration, and this alteration could have pre-dated interaction with the Earth's atmosphere. As one model, we suggest that hypervelocity capture of the impact-related debris by a comet nucleus could have led to shock-wave-induced supercritical aqueous fluids dissolving the silicate, metallic, and organic matter, with later ice sublimation yielding a rocky rubble pile sampled by the meteorite.

DOI： 10.2183/pjab.95.013

Web of Science

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Language：English   Publishing type：Research paper (scientific journal)   Publisher：WILEY  

To precisely determine the abundances of fifty-two elements found within natural water samples, with mass fractions down to fg g(-1) level, we have developed a method which combines freeze-drying pre-concentration (FDC) and isotope dilution internal standardisation (ID-IS). By sublimation of H2O, the sample solution was reduced to < 1/50 of the original volume. To determine element abundance with accuracy better than 10%, we found that for solutions being analysed by mass spectrometry the HNO3 concentration should be > 0.3 mol l(-1) to avoid hydrolysis. Matrix-affected signal suppression was not significant for the solutions with NaCl concentrations lower than 0.2 and 0.1 cg g(-1) for quadrupole ICP-MS and sector field ICP-MS, respectively. The recovery yields of elements after FDC were 97-105%. The detection limits for the sample solutions prepared by FDC were <= 10 pg g(-1), except for Na, K and Ca. Blanks prepared using FDC were at pg-levels, except for eleven elements (Na, Mg, Al, P, Ca, Mn, Fe, Co, Ni, Cu and Zn). The abundances of fifty-two elements in bottled drinking water were determined from five different geological sources with mass fractions ranging from the fg g(-1) to mu g g(-1) level with high accuracy.

DOI： 10.1111/ggr.12245

Web of Science

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Other Link： https://onlinelibrary.wiley.com/doi/full-xml/10.1111/ggr.12245

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