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A large source of low-volatility secondary organic aerosol

机译:低挥发性二次有机气溶胶的大量来源

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森林向大气中排放大量挥发性有机物。森林排放的挥发性有机物的可凝结氧化产物能形成二次有机气溶胶(SOAs),后者能通过散射太阳辐射和充当云凝结核来影响地球的辐射平衡。但我们对源于生物的挥发性有机物与它们向气溶胶颗粒的转化之间联系的认识仍然有限。这项研究显示,一个直接反应通道能导致从挥发性有机物向低挥发性蒸气的转变,后者随后会凝结到气溶胶表面上,产生二次有机气溶胶,并会显著增强林地上空气溶胶颗粒的形成和增长。%Forests emit large quantities of volatile organic compounds (VOCs) to the atmosphere. Their condensable oxidation products can form secondary organic aerosol, a significant and ubiquitous component of atmospheric aerosol, which is known to affect the Earth's radiation balance by scattering solar radiation and by acting as cloud condensation nuclei. The quantitative assessment of such climate effects remains hampered by a number of factors, including an incomplete understanding of how biogenic VOCs contribute to the formation of atmospheric secondary organic aerosol. The growth of newly formed particles from sizes of less than three nanometres up to the sizes of cloud condensation nuclei (about one hundred nanometres) in many continental ecosystems requires abundant, essentially nonvolatile organic vapours, but the sources and compositions of such vapours remain unknown. Here we investigate the oxidation of VOCs, in particular the terpene α-pinene, under atmospherically relevant conditions in chamber experiments. We find that a direct pathway leads from several biogenic VOCs, such as monoterpenes, to the formation of large amounts of extremely low-volatility vapours. These vapours form at significant mass yield in the gas phase and condense irreversibly onto aerosol surfaces to produce secondary organic aerosol, helping to explain the discrepancy between the observed atmospheric burden of secondary organic aerosol and that reported by many model studies. We further demonstrate how these low-volatility vapours can enhance, or even dominate, the formation and growth of aerosol particles over forested regions, providing a missing link between biogenic VOCs and their conversion to aerosol particles. Our findings could help to improve assessments of biosphere-aerosol-climate feedback mechanisms, and the air quality and climate effects of biogenic emissions generally.
机译:森林向大气中排放大量挥发性有机物。森林排放的挥发性有机物的可凝结氧化产物能形成二次有机气溶胶(SOAs),后者能通过散射太阳辐射和充当云凝结核来影响地球的辐射平衡。但我们对源于生物的挥发性有机物与它们向气溶胶颗粒的转化之间联系的认识仍然有限。这项研究显示,一个直接反应通道能导致从挥发性有机物向低挥发性蒸气的转变,后者随后会凝结到气溶胶表面上,产生二次有机气溶胶,并会显着增强林地上空气溶胶颗粒的形成和增长。 %Forests emit large quantities of volatile organic compounds (VOCs) to the atmosphere. Their condensable oxidation products can form secondary organic aerosol, a significant and ubiquitous component of atmospheric aerosol, which is known to affect the Earth's radiation balance by scattering solar radiation and by acting as cloud condensation nuclei. The quantitative assessment of such climate effects remains hampered by a number of factors, including an incomplete understanding of how biogenic VOCs contribute to the formation of atmospheric secondary organic aerosol. The growth of newly formed particles from sizes of less than three nanometres up to the sizes of cloud condensation nuclei (about one hundred nanometres) in many continental ecosystems requires abundant, essentially nonvolatile organic vapours, but the sources and compositions of such vapours remain unknown. Here we investigate the oxidation of VOCs, in particular the terpene α-pinene, under atmospherically relevant condit ions in chamber experiments. We find that a direct pathway leads from several biogenic VOCs, such as monoterpenes, to the formation of large amounts of extremely low-volatility vapours. These vapours form at significant mass yield in the gas phase and condense irreversibly onto aerosol surfaces to produce secondary organic aerosol, helping to explain the discrepancy between the observed atmospheric burden of secondary organic aerosol and that reported by many model studies. We further demonstrate how these low-volatility vapours can enhance, or even dominate, the formation and growth of aerosol particles over forested regions, providing a missing link between biogenic VOCs and their conversion to aerosol particles. Our findings could help to improve assessments of biosphere-aerosol-climate feedback mechanisms, and the air quality and climate effects of biogenic emissions generally.

著录项

  • 来源
    《Nature》 |2014年第7489期|476-479C3|共5页
  • 作者单位

    Institute for Energy and Climate Research (IEK-8), Forschungszentrum Juelich, 52425 Juelich, Germany,Department of Physics, PO Box 64, 00014 University of Helsinki, Finland;

    Department of Physics, PO Box 64, 00014 University of Helsinki, Finland,Department of Atmospheric Sciences, University of Washington, Seattle, Washington 98195, USA;

    Institute of Bio- and Geosciences (IBG-2), Forschungszentrum Julich, 52425 Julich, Germany;

    Department of Physics, PO Box 64, 00014 University of Helsinki, Finland;

    Department of Physics, PO Box 64, 00014 University of Helsinki, Finland;

    Institute for Energy and Climate Research (IEK-8), Forschungszentrum Juelich, 52425 Juelich, Germany;

    Institute for Energy and Climate Research (IEK-8), Forschungszentrum Juelich, 52425 Juelich, Germany;

    Institute for Energy and Climate Research (IEK-8), Forschungszentrum Juelich, 52425 Juelich, Germany;

    Institute for Energy and Climate Research (IEK-8), Forschungszentrum Juelich, 52425 Juelich, Germany;

    Department of Atmospheric Sciences, University of Washington, Seattle, Washington 98195, USA;

    Department of Atmospheric Sciences, University of Washington, Seattle, Washington 98195, USA;

    Institute for Energy and Climate Research (IEK-8), Forschungszentrum Juelich, 52425 Juelich, Germany;

    Institute for Energy and Climate Research (IEK-8), Forschungszentrum Juelich, 52425 Juelich, Germany;

    Department of Physics, PO Box 64, 00014 University of Helsinki, Finland;

    Department of Physics, PO Box 64, 00014 University of Helsinki, Finland,Institute for Tropospheric Research (TR0P0S), 04318 Leipzig, Germany;

    Department of Physics, PO Box 64, 00014 University of Helsinki, Finland;

    Department of Physics, PO Box 64, 00014 University of Helsinki, Finland;

    Department of Physics, PO Box 64, 00014 University of Helsinki, Finland;

    Department of Physics, PO Box 64, 00014 University of Helsinki, Finland,Helsinki Institute of Physics, PO Box 64,00014 University of Helsinki, Finland;

    Department of Chemistry, PO Box 55,00014 University of Helsinki, Finland;

    Department of Chemistry, University of Copenhagen, Universitetsparken 5,2100 Copenhagen O, Denmark;

    Department of Chemistry, University of Copenhagen, Universitetsparken 5,2100 Copenhagen O, Denmark;

    Department of Chemistry, University of Copenhagen, Universitetsparken 5,2100 Copenhagen O, Denmark;

    Aerodyne Research, Inc., 45 Manning Road, Billerica, Massachusetts 01821, USA;

    Department of Physics, Tampere University of Technology, PO Box 692, 33101 Tampere, Finland;

    Institute for Tropospheric Research (TR0P0S), 04318 Leipzig, Germany;

    Department of Physics, PO Box 64, 00014 University of Helsinki, Finland;

    Institute for Energy and Climate Research (IEK-8), Forschungszentrum Juelich, 52425 Juelich, Germany;

    Department of Physics, PO Box 64, 00014 University of Helsinki, Finland;

    Department of Physics, PO Box 64, 00014 University of Helsinki, Finland;

    Department of Physics, PO Box 64, 00014 University of Helsinki, Finland,Aerodyne Research, Inc., 45 Manning Road, Billerica, Massachusetts 01821, USA;

    Institute of Bio- and Geosciences (IBG-2), Forschungszentrum Julich, 52425 Julich, Germany;

    Institute for Energy and Climate Research (IEK-8), Forschungszentrum Juelich, 52425 Juelich, Germany;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
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