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首页> 外文期刊>Atmospheric Chemistry and Physics Discussions >Tropospheric ozone changes, radiative forcing and attribution to emissions in the Atmospheric Chemistry and Climate Model Intercomparison Project (ACCMIP)
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Tropospheric ozone changes, radiative forcing and attribution to emissions in the Atmospheric Chemistry and Climate Model Intercomparison Project (ACCMIP)

机译:在大气化学和气候模式比对项目(ACCMIP)中,对流层臭氧的变化,辐射强迫和排放的归因

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pstrongAbstract./strong Ozone (Osub3/sub) from 17 atmospheric chemistry models taking part in the Atmospheric Chemistry and Climate Model Intercomparison Project (ACCMIP) has been used to calculate tropospheric ozone radiative forcings (RFs). All models applied a common set of anthropogenic emissions, which are better constrained for the present-day than the past. Future anthropogenic emissions follow the four Representative Concentration Pathway (RCP) scenarios, which define a relatively narrow range of possible air pollution emissions. We calculate a value for the pre-industrial (1750) to present-day (2010) tropospheric ozone RF of 410 mW msupa??2/sup. The model range of pre-industrial to present-day changes in Osub3/sub produces a spread (?±1 standard deviation) in RFs of ?±17%. Three different radiation schemes were used a?? we find differences in RFs between schemes (for the same ozone fields) of ?±10%. Applying two different tropopause definitions gives differences in RFs of ?±3%. Given additional (unquantified) uncertainties associated with emissions, climate-chemistry interactions and land-use change, we estimate an overall uncertainty of ?±30% for the tropospheric ozone RF. Experiments carried out by a subset of six models attribute tropospheric ozone RF to increased emissions of methane (44?±12%), nitrogen oxides (31 ?± 9%), carbon monoxide (15 ?± 3%) and non-methane volatile organic compounds (9 ?± 2%); earlier studies attributed more of the tropospheric ozone RF to methane and less to nitrogen oxides. Normalising RFs to changes in tropospheric column ozone, we find a global mean normalised RF of 42 mW msupa??2/sup DUsupa??1/sup, a value similar to previous work. Using normalised RFs and future tropospheric column ozone projections we calculate future tropospheric ozone RFs (mW msupa??2/sup; relative to 1750) for the four future scenarios (RCP2.6, RCP4.5, RCP6.0 and RCP8.5) of 350, 420, 370 and 460 (in 2030), and 200, 300, 280 and 600 (in 2100). Models show some coherent responses of ozone to climate change decreases in the tropical lower troposphere, associated with increases in water vapour; and increases in the sub-tropical to mid-latitude upper troposphere, associated with increases in lightning and stratosphere-to-troposphere transport. Climate change has relatively small impacts on global mean tropospheric ozone RF./p.
机译:> >摘要。已使用来自大气化学和气候模式比较项目(ACCMIP)的17种大气化学模型中的臭氧(O 3 )计算对流层臭氧辐射强迫(RFs)。所有模型都应用了一组常见的人为排放量,与过去相比,今天的排放量受到了更好的限制。未来的人为排放遵循四种代表性浓度途径(RCP)方案,它们定义了可能的空气污染排放范围相对较小的范围。我们计算出从工业化前(1750年)到今天(2010年)对流层臭氧RF的值为410 mW m a ?? 2 。 O 3 的从工业到当前变化的模型范围在RF中产生了±17%的RF扩展(±1标准偏差)。使用了三种不同的辐射方案。我们发现方案(对于相同的臭氧场)之间的RF差异为±10%。采用两种不同的对流层顶定义,RF的差异为±3%。考虑到与排放,气候化学相互作用和土地利用变化相关的其他(未量化)不确定性,我们估计对流层臭氧射频的总体不确定性约为±30%。由六个模型的子集进行的实验将对流层臭氧RF归因于甲烷(44%±12%),氮氧化物(31%±9%),一氧化碳(15%±3%)和非甲烷挥发物的增加排放有机化合物(9±2%);较早的研究将对流层臭氧RF的大部分归因于甲烷,而较少归因于氮氧化物。将RF归一化为对流层臭氧的变化,我们发现42 mW m a ?? 2 DU a ?? 1 的全局平均归一化RF,与先前的工作相似。使用归一化的RF和未来的对流层臭氧预测,我们针对四种未来情况(RCP2.6,RCP4.5,RCP6)计算了未来的对流层臭氧RF(mW m a ?? 2 ;相对于1750)。 0和RCP8.5)分别为350、420、370和460(在2030年),以及200、300、280和600(在2100年)。模型显示,在热带对流层低层,臭氧对气候变化的某些连贯响应与水蒸气的增加有关;在亚热带到中纬度对流层上空增加,这与闪电和平流层到对流层之间的运输增加有关。气候变化对全球平均对流层臭氧RF的影响较小。

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