首页> 外文期刊>Journal of Geophysical Research, D. Atmospheres: JGR >Impacts of climate change on surface ozone and intercontinental ozone pollution: A multi-model study
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Impacts of climate change on surface ozone and intercontinental ozone pollution: A multi-model study

机译:气候变化对地表臭氧和洲际臭氧污染的影响:多模型研究

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The impact of climate change between 2000 and 2095 SRES A2 climates on surface ozone (O)3 and on O3 source-receptor (S-R) relationships is quantified using three coupled climate-chemistry models (CCMs). The CCMs exhibit considerable variability in the spatial extent and location of surface O3 increases that occur within parts of high NOx emission source regions (up to 6 ppbv in the annual average and up to 14 ppbv in the season of maximum O3). In these source regions, all three CCMs show a positive relationship between surface O3 change and temperature change. Sensitivity simulations show that a combination of three individual chemical processes-(i) enhanced PAN decomposition, (ii) higher water vapor concentrations, and (iii) enhanced isoprene emission-largely reproduces the global spatial pattern of annual-mean surface O3 response due to climate change (R2 = 0.52). Changes in climate are found to exert a stronger control on the annual-mean surface O3 response through changes in climate-sensitive O3 chemistry than through changes in transport as evaluated from idealized CO-like tracer concentrations. All three CCMs exhibit a similar spatial pattern of annual-mean surface O3 change to 20% regional O3 precursor emission reductions under future climate compared to the same emission reductions applied under present-day climate. The surface O3 response to emission reductions is larger over the source region and smaller downwind in the future than under present-day conditions. All three CCMs show areas within Europe where regional emission reductions larger than 20% are required to compensate climate change impacts on annual-mean surface O3.
机译:使用三个耦合的气候化学模型(CCM)量化了2000年至2095年SRES A2气候之间的气候变化对地面臭氧(O)3和对O3源-受体(S-R)关系的影响。 CCMs在高NOx排放源区域的一部分中发生的表面O3的空间范围和位置变化表现出相当大的可变性(年平均最高6 ppbv,最大O3的季节最高14 ppbv)。在这些源区中,所有三个CCM都显示出表面O3变化与温度变化之间的正相关关系。敏感性模拟显示,三个独立的化学过程的组合-(i)增强的PAN分解,(ii)较高的水蒸气浓度和(iii)增强的异戊二烯排放-很大程度上重现了年均表面O3响应的全球空间格局,这是由于气候变化(R2 = 0.52)。发现气候变化通过对气候敏感的O3化学物质的变化,比通过从理想的类似CO的示踪剂浓度评估的运输变化,对年平均表面O3响应的控制更强。与当前气候下采用的相同减排量相比,未来气候下所有三个CCM均表现出相似的年均表面臭氧变化空间格局,区域O3前体排放量减少了20%。与当前条件相比,未来地表O3对排放量减少的响应在源区域更大,而下风向更小。所有这三个CCM都显示出欧洲范围内需要将区域减排量超过20%的区域,以补偿气候变化对年平均O3的影响。

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