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首页> 外文期刊>Atmospheric chemistry and physics >Rapid increase in summer surface ozone over the North China Plain during 2013–2019: a side effect of particulate matter reduction control?
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Rapid increase in summer surface ozone over the North China Plain during 2013–2019: a side effect of particulate matter reduction control?

机译:2013 - 2019年中国华北平原夏季臭氧快速增加:颗粒物还原对照的副作用吗?

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摘要

While the elevated ambient levels of particulate matters with aerodynamic diameter of 2.5? μ m or less (PM 2.5 ) are alleviated largely with the implementation of effective emission control measures, an opposite trend with a rapid increase has been seen in surface ozone (O 3 ) in the North China Plain (NCP) region over the past several years. It is critical to determine the real culprit causing such a large increase in surface O 3 . In this study, 7-year surface observations and satellite retrieval data are analyzed to determine the long-term change in surface O 3 as well as driving factors. Results indicate that anthropogenic emission control strategies and changes in aerosol concentrations as well as aerosol optical properties such as single-scattering albedo (SSA) are the most important factors driving such a large increase in surface O 3 . Numerical simulations with the National Center for Atmospheric Research (NCAR) Master Mechanism (MM) model suggest that reduction of O 3 precursor emissions and aerosol radiative effect accounted for 45?% and 23?% of the total change in surface O 3 in summertime during 2013–2019, respectively. Planetary boundary layer (PBL) height with an increase of 0.21?km and surface air temperature with an increase of 2.1? ° C contributed 18?% and 12?% to the total change in surface O 3 , respectively. The combined effect of these factors was responsible for the rest of the change. Decrease in SSA or strengthened absorption property of aerosols may offset the impact of aerosol optical depth (AOD) reduction on surface O 3 substantially. While the MM model enables quantification of an individual factor's percentage contributions, it requires further refinement with aerosol chemistry included in the future investigation. The study indicates an important role of aerosol radiative effect in development of more effective emission control strategies on reduction of ambient levels of O 3 as well as alleviation of national air quality standard exceedance events.
机译:虽然高温的环境水平颗粒物质的气动直径为2.5? μM或更小(PM 2.5)在很大程度上缓解了有效排放控制措施的实施,在过去几个地区的华北平原(NCP)地区的表面臭氧(O 3)中已经看到了相反的趋势年。确定真正的罪魁祸首,导致表面o 3的这种大幅增加至关重要。在本研究中,分析了7年的表面观察和卫星检索数据以确定表面O 3的长期变化以及驱动因子。结果表明,气溶胶浓度以及气溶胶光学性质如单散射玻璃(SSA)的人为排放控制策略及气溶胶光学性质是驱动表面O 3大幅增加的最重要因素。与国家大气研究中心的数值模拟(NCAR)母部机制(MM)模型表明O 3前体排放和气溶胶辐射效果的降低占Sumpertime的表面O 3总变化的45?%和23?%分别为本2013-2019。行星边界层(PBL)高度,增加0.21 km和表面空气温度,增加2.1? °C分别为表面O 3的总变化贡献18℃。这些因素的综合效果负责其余的变化。 SSA的降低或气溶胶的增强的吸收性能可能抵消气溶胶光学深度(AOD)降低的影响基本上3的影响。虽然MM模型能够量化个别因素的百分比贡献,但它需要进一步改进未来调查中的气溶胶化学。该研究表明了气溶胶辐射效应在开发更有效的排放控制策略方面的重要作用,减少了o 3的环境水平以及减轻国家空气质量标准的超标事件。

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