Articles | Volume 35, issue 5
https://doi.org/10.5194/ejm-35-813-2023
© Author(s) 2023. This work is distributed under
the Creative Commons Attribution 4.0 License.
the Creative Commons Attribution 4.0 License.
https://doi.org/10.5194/ejm-35-813-2023
© Author(s) 2023. This work is distributed under
the Creative Commons Attribution 4.0 License.
the Creative Commons Attribution 4.0 License.
Research article
| Highlight paper
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04 Oct 2023
Research article | Highlight paper |
| 04 Oct 2023
| 04 Oct 2023
Depth profile analyses by femtosecond laser ablation (multicollector) inductively coupled plasma mass spectrometry for resolving chemical and isotopic gradients in minerals
Martin Oeser
CORRESPONDING AUTHOR
Institut für Mineralogie, Leibniz Universität Hannover,
Callinstr. 3, 30167 Hanover, Germany
Ingo Horn
Institut für Mineralogie, Leibniz Universität Hannover,
Callinstr. 3, 30167 Hanover, Germany
Ralf Dohmen
Institut für Geologie, Mineralogie und Geophysik, Ruhr-Universität Bochum, Universitätsstr. 150, 44801 Bochum, Germany
Stefan Weyer
Institut für Mineralogie, Leibniz Universität Hannover,
Callinstr. 3, 30167 Hanover, Germany
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Roxane Buso, Didier Laporte, Federica Schiavi, Nicolas Cluzel, and Claire Fonquernie
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Carla Tiraboschi, Francesca Miozzi, and Simone Tumiati
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Enrico Cannaò, Massimo Tiepolo, Giulio Borghini, Antonio Langone, and Patrizia Fumagalli
Eur. J. Mineral., 34, 35–57, https://doi.org/10.5194/ejm-34-35-2022, https://doi.org/10.5194/ejm-34-35-2022, 2022
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Amphibole–liquid partitioning of elements of geological relevance is experimentally derived at conditions compatible with those of the Earth's upper mantle. Experiments are carried out at different oxygen fugacity conditions and variable Cl content in order to investigate their influence on the amphibole–liquid partition coefficients. Our results point to the capability of amphibole to act as filter for trace elements at upper-mantle conditions, oxidized conditions, and Cl-rich environments.
Enrico Cannaò, Federica Schiavi, Giulia Casiraghi, Massimo Tiepolo, and Patrizia Fumagalli
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Detailed knowledge of the mechanisms ruling water incorporation in amphibole is essential to understand how much water can be fixed at upper-mantle conditions by this mineral. We provide the experimental evidence of the Cl effect on the oxo-substitution and the incorporation of water in amphibole. Finally, we highlight the versatility of confocal micro-Raman spectroscopy as an analytical tool to quantify water in amphibole.
Michael C. Jollands, Hugh St.C. O'Neill, Andrew J. Berry, Charles Le Losq, Camille Rivard, and Jörg Hermann
Eur. J. Mineral., 33, 113–138, https://doi.org/10.5194/ejm-33-113-2021, https://doi.org/10.5194/ejm-33-113-2021, 2021
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How, and how fast, does hydrogen move through crystals? We consider this question by adding hydrogen, by diffusion, to synthetic crystals of olivine doped with trace amounts of chromium. Even in a highly simplified system, the behaviour of hydrogen is complex. Hydrogen can move into and through the crystal using various pathways (different defects within the crystal) and hop between these pathways too.
Joana Polednia, Ralf Dohmen, and Katharina Marquardt
Eur. J. Mineral., 32, 675–696, https://doi.org/10.5194/ejm-32-675-2020, https://doi.org/10.5194/ejm-32-675-2020, 2020
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Grain boundary diffusion is orders of magnitude faster compared to volume diffusion. We studied this fast transport process in a well-defined garnet grain boundary. State-of-the-art microscopy was used for quantification. A dedicated numerical diffusion model shows that iron diffusion requires the operation of two diffusion modes, one fast, one slow. We conclude that impurity bulk diffusion in garnet aggregates is always dominated by grain boundary diffusion.
Giulio Borghini and Patrizia Fumagalli
Eur. J. Mineral., 32, 251–264, https://doi.org/10.5194/ejm-32-251-2020, https://doi.org/10.5194/ejm-32-251-2020, 2020
Alan B. Woodland, Andrei V. Girnis, Vadim K. Bulatov, Gerhard P. Brey, and Heidi E. Höfer
Eur. J. Mineral., 32, 171–185, https://doi.org/10.5194/ejm-32-171-2020, https://doi.org/10.5194/ejm-32-171-2020, 2020
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We experimentally explored direct entrapment of breyite (CaSiO3) by diamond at upper-mantle conditions in a model subducted sediment rather than formation by retrogression of CaSiO3 perovskite, implying a deeper origin. Anhydrous low-T melting of CaCO3+SiO2 precludes breyite formation. Under hydrous conditions, reduction of melt results in graphite with breyite. Thus, breyite inclusions in natural diamond may form from aragonite + coesite or carbonate melt at 6–8 GPa via reduction with water.
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Short summary
This study presents a new method designed to analyze micrometer-scale chemical and isotopic profiles in minerals, glasses, and other solids. The employed technique combines plasma mass spectrometers and a state-of-the-art femtosecond laser equipped with open-source software (LinuxCNC) that controls the movement of the laser beam. It allows for equably drilling into the sample surface, e.g., in order to measure chemically or isotopically zoned or heterogeneous materials at micrometer scales.
This study presents a new method designed to analyze micrometer-scale chemical and isotopic...
