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Singular vector decomposition for sensitivity analyses of tropospheric chemical scenarios

机译:对流层化学场景敏感性分析的奇异载体分解

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Observations of the chemical state of the atmosphere typically provide only sparse snapshots of the state of the system due to their insufficient temporal and spatial density. One possibility for optimisation of the state estimate is to target the observation of those parameters that have the largest potential of resulting in forecast improvements. In the present work, the technique of singular vector analysis is applied to atmospheric chemical modelling in order to identify the most sensitive chemical compounds during a given time period and prioritise them for measurement. Novel to the current work is the fact that, in the application of singular vector analysis, not only the initial values but also the emissions are considered as target variables for adaptive observation strategies. This specific application of singular vector analysis is studied in the context of a chemistry box model allowing for validation of its new features for two chemical regimes. The time and regime dependence of the ozone (O3) and peroxyacetyl nitrate (PAN) formation potential of individual volatile organic compounds (VOCs) is investigated. Results show that the combined sensitivity of O3 and PAN to individual VOCs is strongly dependent on the photochemical scenario and simulation interval used. Particularly the alkanes show increasing sensitivities with increasing simulation length. Classifying the VOCs as being of high, medium, little or negligible importance for the formation of O3 and PAN allows for the identification of those VOCs that may be omitted from measurement. We find that it is possible to omit 6 out of 18 VOCs considered for initial value measurement and 4 out of 12 VOCs considered for emission measurement. The omission of these VOCs is independent of photochemical regime and simulation length. The VOCs selected for measuring account for more than 96% and 90% of the O3 and PAN sensitivity to VOCs, respectively.
机译:对大气的化学状态的观察通常仅提供系统状态的稀疏快照,因为它们不足的时间和空间密度。优化状态估计的一种可能性是瞄准观察那些具有导致预测改善的最大潜力的参数。在本作工作中,奇异载体分析技术应用于大气化学模型,以便在给定的时间段内鉴定最敏感的化学化合物,并优先考虑它们进行测量。新颖的目前的工作是事实上,在奇异载体分析的应用中,不仅是初始值,而且将排放量视为适应性观察策略的目标变量。在化学盒式模型的背景下研究了奇异载体分析的这种特异性应用,允许验证其两个化学制度的新功能。研究了臭氧(O 3)和硝酸过氧基乙酯(PAN)形成电位的臭氧(O 3)和过氧乙酰基的硝酸盐(VOC)的时间和体状依赖性。结果表明,O3和PAN对各个VOC的组合敏感性强烈依赖于所使用的光化学场景和模拟间隔。特别是烷烃呈增加敏感度随着模拟长度的增加而增加。将VOC分类为高,培养基,少于或可以忽略不计的O3和PAN的重要性允许识别可能从测量中省略的那些VOC。我们发现,在考虑用于初始值测量的18个VOC中可以省略6个,其中4个VOC中的4个被考虑的排放测量。这些VOC的遗漏与光化学制度和模拟长度无关。选择的VOCS用于测量占O3的超过96%和90%,并分别对VOC的敏感性。

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