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The impact of biogenic, anthropogenic, and biomass burning volatile organic compound emissions on regional and seasonal variations in secondary organic aerosol

机译:生物,人为和生物质燃烧挥发性有机化合物排放对次级有机气溶胶区域和季节变异的影响

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The global secondary organic aerosol (SOA) budget is highly uncertain, with global annual SOA production rates, estimated from global models, ranging over an order of magnitude and simulated SOA concentrations underestimated compared to observations. In this study, we use a global composition-climate model (UKCA) with interactive chemistry and aerosol microphysics to provide an indepth analysis of the impact of each VOC source on the global SOA budget and its seasonality. We further quantify the role of each source on SOA spatial distributions, and evaluate simulated seasonal SOA concentrations against a comprehensive set of observations. The annual global SOA production rates from monoterpene, isoprene, biomass burning, and anthropogenic precursor sources is 19.9, 19.6, 9.5, and 24.6 Tg. SOA / a 1, respectively. When all sources are included, the SOA production rate from all sources is 73.6 Tg (SOA) a(-1), which lies within the range of estimates from previous modelling studies. SOA production rates and SOA burdens from biogenic and biomass burning SOA sources peak during Northern Hemisphere (NH) summer. In contrast, the anthropogenic SOA production rate is fairly constant all year round. However, the global anthropogenic SOA burden does have a seasonal cycle which is lowest during NH summer, which is probably due to enhanced wet removal. Inclusion of the new SOA sources also accelerates the ageing by condensation of primary organic aerosol (POA), making it more hydrophilic, leading to a reduction in the POA lifetime. With monoterpene as the only source of SOA, simulated SOA and total organic aerosol (OA) concentrations are underestimated by the model when compared to surface and aircraft measurements. Model agreement with observations improves with all new sources added, primarily due to the inclusion of the anthropogenic source of SOA, although a negative bias remains. A further sensitivity simulation was performed with an increased anthropogenic SOA reaction yie
机译:全球二次有机气溶胶(SOA)预算高度不确定,全球年度SOA生产率从全球模型估计,与观察结果相比低估的数量级和模拟SOA浓度。在这项研究中,我们使用全球性质 - 气候模型(UKCA)与互动化学和气溶胶微生物质,为每个VOC来源对全球SOA预算及其季节性的影响提供了深入的分析。我们进一步量化了每个来源对SOA空间分布的作用,并评估模拟季节性SOA浓度,以综合观察。从单萜,异戊二烯,生物质燃烧和人为前体来源的年度全球SOA产量为19.9,19.6,9.5和24.6 Tg。 SOA / A 1分别。当包括所有来源时,来自所有来源的SOA生产率为73.6 Tg(SOA)A(-1),其在以前建模研究的估算范围内。 SOA生产率和SOA来自生物和生物量燃烧SOA北半球(NH)夏季的峰值峰值。相比之下,全年人为的SOA生产率相当恒定。然而,全球人为的SOA负担确实在NH夏季最低的季节性循环,这可能是由于增强的湿式去除。包含新的SOA源也通过初级有机气溶胶(POA)的冷凝加速了衰老,使其更亲水,导致POA寿命减少。与SOA的唯一源单调源,模拟与表面和飞机测量相比,模型低估了模拟SOA和总有机气溶胶(OA)浓度。与观察结果的模型协议改善了所有新的来源,主要是由于含有SOA的人为来源,尽管仍然存在负面偏见。通过增加的人为SOA反应致远进行进一步的敏感性模拟

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