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Mercury isotope evidence for Arctic summertime re-emission of mercury from the cryosphere

Author

Listed:
  • Beatriz Ferreira Araujo

    (Université de Toulouse)

  • Stefan Osterwalder

    (ETH Zurich
    CNRS, IRD, Grenoble INP, IGE)

  • Natalie Szponar

    (University of Toronto)

  • Domenica Lee

    (University of Toronto)

  • Mariia V. Petrova

    (Mediterranean Institute of Oceanography)

  • Jakob Boyd Pernov

    (Aarhus University
    École Polytechnique fédérale de Lausanne)

  • Shaddy Ahmed

    (CNRS, IRD, Grenoble INP, IGE)

  • Lars-Eric Heimbürger-Boavida

    (Mediterranean Institute of Oceanography)

  • Laure Laffont

    (Université de Toulouse)

  • Roman Teisserenc

    (Laboratoire Écologie Fonctionnelle et Environnement)

  • Nikita Tananaev

    (Russian Academy of Sciences
    North-Eastern Federal University)

  • Claus Nordstrom

    (Aarhus University)

  • Olivier Magand

    (CNRS, IRD, Grenoble INP, IGE)

  • Geoff Stupple

    (Environment and Climate Change Canada)

  • Henrik Skov

    (Aarhus University)

  • Alexandra Steffen

    (Environment and Climate Change Canada)

  • Bridget Bergquist

    (University of Toronto)

  • Katrine Aspmo Pfaffhuber

    (Norwegian Institute for Air Research)

  • Jennie L. Thomas

    (CNRS, IRD, Grenoble INP, IGE)

  • Simon Scheper

    (Dr. Simon Scheper—Research | Consulting | Teaching
    University of Basel)

  • Tuukka Petäjä

    (University of Helsinki)

  • Aurélien Dommergue

    (CNRS, IRD, Grenoble INP, IGE)

  • Jeroen E. Sonke

    (Université de Toulouse)

Abstract

During Arctic springtime, halogen radicals oxidize atmospheric elemental mercury (Hg0), which deposits to the cryosphere. This is followed by a summertime atmospheric Hg0 peak that is thought to result mostly from terrestrial Hg inputs to the Arctic Ocean, followed by photoreduction and emission to air. The large terrestrial Hg contribution to the Arctic Ocean and global atmosphere has raised concern over the potential release of permafrost Hg, via rivers and coastal erosion, with Arctic warming. Here we investigate Hg isotope variability of Arctic atmospheric, marine, and terrestrial Hg. We observe highly characteristic Hg isotope signatures during the summertime peak that reflect re-emission of Hg deposited to the cryosphere during spring. Air mass back trajectories support a cryospheric Hg emission source but no major terrestrial source. This implies that terrestrial Hg inputs to the Arctic Ocean remain in the marine ecosystem, without substantial loss to the global atmosphere, but with possible effects on food webs.

Suggested Citation

  • Beatriz Ferreira Araujo & Stefan Osterwalder & Natalie Szponar & Domenica Lee & Mariia V. Petrova & Jakob Boyd Pernov & Shaddy Ahmed & Lars-Eric Heimbürger-Boavida & Laure Laffont & Roman Teisserenc &, 2022. "Mercury isotope evidence for Arctic summertime re-emission of mercury from the cryosphere," Nature Communications, Nature, vol. 13(1), pages 1-12, December.
  • Handle: RePEc:nat:natcom:v:13:y:2022:i:1:d:10.1038_s41467-022-32440-8
    DOI: 10.1038/s41467-022-32440-8
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    References listed on IDEAS

    as
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    2. Seung Hyeon Lim & Younggwang Kim & Laura C. Motta & Eun Jin Yang & Tae Siek Rhee & Jong Kuk Hong & Seunghee Han & Sae Yun Kwon, 2024. "Near surface oxidation of elemental mercury leads to mercury exposure in the Arctic Ocean biota," Nature Communications, Nature, vol. 15(1), pages 1-11, December.
    3. Hailong Li & Fanyue Meng & Penglin Zhu & Hongxiao Zu & Zequn Yang & Wenqi Qu & Jianping Yang, 2024. "Biomimetic mercury immobilization by selenium functionalized polyphenylene sulfide fabric," Nature Communications, Nature, vol. 15(1), pages 1-15, December.

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