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Nanoscale silicate melt textures determine volcanic ash surface chemistry

Author

Listed:
  • Adrian J. Hornby

    (Cornell University
    Ludwig-Maximilians-Universtität (LMU))

  • Paul M. Ayris

    (Ludwig-Maximilians-Universtität (LMU))

  • David E. Damby

    (U.S. Geological Survey, Volcano Science Center)

  • Spyridon Diplas

    (Material Physics Oslo, SINTEF Industry)

  • Julia Eychenne

    (Université Clermont Auvergne, CNRS, IRD, OPGC, Laboratoire Magmas et Volcans
    Université Clermont Auvergne, CNRS, INSERM, Institut de Génétique Reproduction et Développement)

  • Jackie E. Kendrick

    (Ludwig-Maximilians-Universtität (LMU))

  • Corrado Cimarelli

    (Ludwig-Maximilians-Universtität (LMU))

  • Ulrich Kueppers

    (Ludwig-Maximilians-Universtität (LMU))

  • Bettina Scheu

    (Ludwig-Maximilians-Universtität (LMU))

  • James E. P. Utley

    (University of Liverpool)

  • Donald B. Dingwell

    (Ludwig-Maximilians-Universtität (LMU))

Abstract

Explosive volcanic eruptions produce vast quantities of silicate ash, whose surfaces are subsequently altered during atmospheric transit. These altered surfaces mediate environmental interactions, including atmospheric ice nucleation, and toxic effects in biota. A lack of knowledge of the initial, pre-altered ash surface has required previous studies to assume that the ash surface composition created during magmatic fragmentation is equivalent to the bulk particle assemblage. Here we examine ash particles generated by controlled fragmentation of andesite and find that fragmentation generates ash particles with substantial differences in surface chemistry. We attribute this disparity to observations of nanoscale melt heterogeneities, in which Fe-rich nanophases in the magmatic melt deflect and blunt fractures, thereby focusing fracture propagation within aureoles of single-phase melt formed during diffusion-limited growth of crystals. In this manner, we argue that commonly observed pre-eruptive microtextures caused by disequilibrium crystallisation and/or melt unmixing can modify fracture propagation and generate primary discrepancies in ash surface chemistry, an essential consideration for understanding the cascading consequences of reactive ash surfaces in various environments.

Suggested Citation

  • Adrian J. Hornby & Paul M. Ayris & David E. Damby & Spyridon Diplas & Julia Eychenne & Jackie E. Kendrick & Corrado Cimarelli & Ulrich Kueppers & Bettina Scheu & James E. P. Utley & Donald B. Dingwell, 2024. "Nanoscale silicate melt textures determine volcanic ash surface chemistry," Nature Communications, Nature, vol. 15(1), pages 1-10, December.
  • Handle: RePEc:nat:natcom:v:15:y:2024:i:1:d:10.1038_s41467-024-44712-6
    DOI: 10.1038/s41467-024-44712-6
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    References listed on IDEAS

    as
    1. Mike Cassidy & Michael Manga & Kathy Cashman & Olivier Bachmann, 2018. "Controls on explosive-effusive volcanic eruption styles," Nature Communications, Nature, vol. 9(1), pages 1-16, December.
    2. Victoria C. Honour & Marian B. Holness & Bernard Charlier & Sandra C. Piazolo & Olivier Namur & Ty J. Prosa & Isabelle Martin & Rosalind T. Helz & John Maclennan & Marlon M. Jean, 2019. "Compositional boundary layers trigger liquid unmixing in a basaltic crystal mush," Nature Communications, Nature, vol. 10(1), pages 1-8, December.
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