4.7 Article

Investigations on the anthropogenic reversal of the natural ozone gradient between northern and southern midlatitudes

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ATMOSPHERIC CHEMISTRY AND PHYSICS
卷 21, 期 12, 页码 9669-9679

出版社

COPERNICUS GESELLSCHAFT MBH
DOI: 10.5194/acp-21-9669-2021

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资金

  1. NOAA's Atmospheric Chemistry and Climate Program
  2. BEIS
  3. DEFRA Met Office Hadley Centre Climate Programme [GA01101]
  4. UK-China Research and Innovation Partnership Fund through the Met Office Climate Science for Service Partnership (CSSP) China as part of the Newton Fund
  5. Japan Society for the Promotion of Science KAKENHI [JP18H03363, JP18H05292, JP20K04070]
  6. Environment Research and Technology Development Fund of the Environmental Restoration and Conservation Agency of Japan [JPMEERF20172003, JPMEERF20202003, JPMEERF20205001]
  7. Arctic Challenge for Sustainability II (ArCS II), program [JPMXD1420318865]
  8. National Science Foundation

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Our understanding of natural tropospheric ozone concentrations has been limited by the lack of reliable measurements before the 1980s. Observations suggest that ozone concentrations in the Northern Hemisphere have been increasing at a faster rate than in the Southern Hemisphere, primarily due to anthropogenic emissions of ozone precursors. Earth system model simulations also indicate a similar trend, but uncertainties in the models may lead to disagreements with observational data.
Our quantitative understanding of natural tropospheric ozone concentrations is limited by the paucity of reliable measurements before the 1980s. We utilize the existing measurements to compare the long-term ozone changes that occurred within the marine boundary layer at northern and southern midlatitudes. Since 1950 ozone concentrations have increased by a factor of 2.1 +/- 0.2 in the Northern Hemisphere (NH) and are presently larger than in the Southern Hemisphere (SH), where only a much smaller increase has occurred. These changes are attributed to increased ozone production driven by anthropogenic emissions of photochemical ozone precursors that increased with industrial development. The greater ozone concentrations and increases in the NH are consistent with the predominant location of anthropogenic emission sources in that hemisphere. The available measurements indicate that this interhemispheric gradient was much smaller and was likely reversed in the preindustrial troposphere with higher concentrations in the SH. Six Earth system model (ESM) simulations indicate similar total NH increases (1.9 with a standard deviation of 0.3), but they occurred more slowly over a longer time period, and the ESMs do not find higher pre-industrial ozone in the SH. Several uncertainties in the ESMs may cause these model- measurement disagreements: the assumed natural nitrogen oxide emissions may be too large, the relatively greater fraction of ozone injected by stratosphere-troposphere exchange to the NH may be overestimated, ozone surface deposition to ocean and land surfaces may not be accurately simulated, and model treatment of emissions of biogenic hydrocarbons and their photochemistry may not be adequate.

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