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Bates, Kelvin

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Bates

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Kelvin

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Bates, Kelvin

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Now showing 1 - 2 of 2
  • Publication

    Satellite isoprene retrievals constrain emissions and atmospheric oxidation

    (Springer Science and Business Media LLC, 2020-09-09) Wells, Kelley C.; Millet, Dylan B.; Payne, Vivienne H.; Deventer, M. Julian; Bates, Kelvin; de Gouw, Joost A.; Graus, Martin; Warneke, Carsten; Wisthaler, Armin; Fuentes, Jose D.; Fuentes

    Isoprene is the dominant non-methane organic compound emitted to the atmosphere. It drives ozone and aerosol production, modulates atmospheric oxidation, and interacts with the global nitrogen cycle. Isoprene emissions are highly uncertain, as is the non-linear chemistry coupling isoprene and the hydroxyl radical, OH — its primary sink. Here we present the first global isoprene measurements from space, using the Cross-track Infrared Sounder (CrIS). These isoprene measurements, together with observations of its oxidation product formaldehyde, provide new constraints on isoprene emissions and atmospheric oxidation. We find that isoprene:formaldehyde relationships measured from space are broadly consistent with current understanding of isoprene-OH chemistry, with no indication of missing OH recycling at low-NOx. We analyze these datasets over four global isoprene hotspots in relation to model predictions, and present a first demonstration of isoprene emission quantification based directly on satellite measurements of isoprene itself. A major discrepancy emerges over Amazonia, where current underestimates of natural NOx emissions bias modeled OH and hence isoprene. Over southern Africa, we find that a prominent isoprene hotspot is missing from bottom-up predictions. A multi-year analysis sheds light on interannual isoprene variability, and suggests the role of El Niño.

  • Publication

    A Two-Pollutant Strategy for Improving Ozone and Particulate Air Quality in China

    (Springer Science and Business Media LLC, 2019-10-14) Li, Ke; Jacob, Daniel; Liao, Hong; Zhu, Jia; Shah, Viral; Shen, Lu; Bates, Kelvin; Zhang, Qiang; Zhai, Shixian

    Fine particulate matter (PM2.5) decreased by 30–40% across China over the 2013–2017 period in response to the governmental Clean Air Action. However, surface ozone pollution worsened over the same period. Model simulations have suggested that the increase of ozone could be driven by the decrease in PM2.5, because PM2.5 scavenges hydroperoxy (HO2) and nitrogen oxide (NOx) radicals that otherwise produce ozone. Here we show observational evidence for this effect with 2013–2018 summer data of hourly ozone and PM2.5 concentrations from 106 sites in the North China Plain. The observations show suppression of ozone pollution at high PM2.5 concentrations, consistent with a model simulation in which PM2.5 scavenging of HO2 and NOx depresses ozone concentrations by 25 ppb relative to PM2.5-free conditions. PM2.5 chemistry makes ozone pollution less sensitive to NOx emission controls, emphasizing the need for controlling emissions of volatile organic compounds (VOCs) which so far have not decreased in China. The new 2018–2020 Clean Air Action calls for a 10% decrease in VOC emissions that should begin to reverse the long-term ozone increase even as PM2.5 continues to decrease. Aggressive reduction of NOx and aromatic VOC emissions should be particularly effective for decreasing both PM2.5 and ozone.