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首页> 外文期刊>Journal of Geophysical Research. Biogeosciences >A mass-balance/photochemical assessment of DMS sea-to-air flux as inferred from NASA GTE PEM-West A and B observations
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A mass-balance/photochemical assessment of DMS sea-to-air flux as inferred from NASA GTE PEM-West A and B observations

机译:根据NASA GTE PEM-West A和B观测结果推断的DMS海空通量的质量平衡/光化学评估

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摘要

This study reports dimethyl sulfide (DMS) sea-to-air fluxes derived from a mass-balance/photochemical-modeling approach. The region investigated was the western North Pacific covering the latitude range of 0 deg-30 deg N. Two NASA airborne databases were used in this study: PEM-West A in September-October 1991 and PEM-West B in February-March 1994. A total of 35 boundary layer (BL) sampling runs were recorded between the two programs. However, after filtering these data for pollution impacts and DMS lifetime considerations, this total was reduced to 13. Input for each analysis consisted of atmospheric DMS measurements, the equivalent mixing depth (EMD) for DMS, and model estimated values for OH and NO_3. The evaluation of the EMD took into account both DMS within the BL as well as that transported into the overlying atmospheric buffer layer (BuL). DMS fluxes ranged from 0.6 to 3.0 #mu#mol m~(-2) d~(-1) for PEM-West A (10 sample runs) and 1.4 to 1.9 #mu#mol m~(-2) d~(-1) for PEM-West B (3 sample runs). Sensitivity analyses showed that the photochemically evaluated DMS flux was most influenced by the DMS vertical profile and the diel profile for OH. A propagation of error analysis revealed that the uncertainty associated with individual flux determinations ranged from a factor of 1.3 to 1.5. Also assessed were potential systematic errors. The first of these relates to our noninclusion of large-scale mean vertical motion as it might appear in the form of atmospheric subsidence or as a convergence. Our estimates here would place this error in the range of 0 to 30%. By far the largest systematic error is that associated with stochastic events (e.g., those involving major changes in cloud coverage). In the latter case, sensitivity tests suggested that the error could be as high as a factor of 2. With improvements in such areas as BL sampling time, direct observations of OH, improved DMS vertical profiling, direct assessment of vertical velocity in the field, and preflight (24 hours) detailed meteorological data, it appears that the uncertainty in this approach could be reduced to +- 25%.
机译:这项研究报告了源自质量平衡/光化学建模方法的二甲基硫醚(DMS)海对空气通量。被调查的地区是北太平洋西部,北纬0度到北纬30度。本研究使用了两个NASA机载数据库:1991年9月至10月的PEM-West A和1994年2月至3月的PEM-WestB。两个程序之间总共记录了35个边界层(BL)采样运行。但是,在对这些数据进行了污染影响和DMS寿命考虑因素过滤后,总数减少到13。每次分析的输入包括大气DMS测量值,DMS的等效混合深度(EMD)以及OH和NO_3的模型估计值。 EMD的评估考虑了BL中的DMS以及传输到上方大气缓冲层(BuL)中的DMS。对于PEM-West A(10个样品运行),DMS通量范围为0.6至3.0#mu#mol m〜(-2)d〜(-1)和1.4至1.9#mu#mol m〜(-2)d〜( -1)用于PEM-West B(3个样品运行)。敏感性分析表明,光化学评估的DMS通量受DMS垂直分布和OH的diel分布影响最大。误差分析的传播表明,与单个通量确定相关的不确定性范围为1.3到1.5。还评估了潜在的系统错误。第一个与我们不包括大规模平均垂直运动有关,因为它可能以大气下陷或会聚的形式出现。我们在这里的估计值将使此错误的范围为0到30%。到目前为止,最大的系统错误是与随机事件相关的错误(例如,涉及云覆盖率重大变化的错误)。在后一种情况下,灵敏度测试表明误差可能高达2倍。随着诸如BL采样时间,OH的直接观测,改进的DMS垂直分布图,现场垂直速度的直接评估,和飞行前(24小时)的详细气象数据,看来这种方法的不确定性可以降低到+-25%。

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