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首页> 外文期刊>Journal of Geophysical Research, D. Atmospheres: JGR >HO_x chemistry during INTEX-A 2004: Observation, model calculation, and comparison with previous studies
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HO_x chemistry during INTEX-A 2004: Observation, model calculation, and comparison with previous studies

机译:INTEX-A 2004期间的HO_x化学:观察,模型计算以及与先前研究的比较

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摘要

OH and HO2 were measured with the Airborne Tropospheric Hydrogen Oxides Sensor (ATHOS) as part of a large measurement suite from the NASA DC-8 aircraft during the Intercontinental Chemical Transport Experiment-A (INTEX-A). This mission, which was conducted mainly over North America and the western Atlantic Ocean in summer 2004, was an excellent test of atmospheric oxidation chemistry. The HOx results from INTEX-A are compared to those from previous campaigns and to results for other related measurements from INTEX-A. Throughout the troposphere, observed OH was generally 0.95 of modeled OH; below 8 km, observed HO2 was generally 1.20 of modeled HO2. This observed-to-modeled comparison is similar to that for TRACE-P, another midlatitude study for which the median observed-to-modeled ratio was 1.08 for OH and 1.34 for HO2, and to that for PEM-TB, a tropical study for which the median observed-to-modeled ratio was 1.17 for OH and 0.97 for HO2. HO2 behavior above 8 km was markedly different. The observed-to-modeled HO2 ratio increased from ~1.2 at 8 km to ~3 at 11 km with the observed-to-modeled ratio correlating with NO. Above 8 km, the observed-to-modeled HO2 and observed NO were both considerably greater than observations from previous campaigns. In addition, the observed-to-modeled HO2/OH, which is sensitive to cycling reactions between OH and HO2, increased from ~1.5 at 8 km to almost 3.5 at 11 km. These discrepancies suggest a large unknown HO x source and additional reactants that cycle HO x from OH to HO2. In the continental planetary boundary layer, the observed-to-modeled OH ratio increased from 1 when isoprene was less than 0.1 ppbv to over 4 when isoprene was greater than 2 ppbv, suggesting that forests throughout the United States are emitting unknown HO x sources. Progress in resolving these discrepancies requires a focused research activity devoted to further examination of possible unknown OH sinks and HO x sources.
机译:在洲际化学品运输实验A(INTEX-A)期间,作为对NASA DC-8飞机的大型测量套件的一部分,使用机载对流层氧化氢传感器(ATHOS)测量了OH和HO2。该任务于2004年夏季主要在北美和西大西洋上空进行,是对大气氧化化学反应的出色测试。将INTEX-A的HOx结果与以前的测试结果进行比较,并与INTEX-A的其他相关测量结果进行比较。在整个对流层中,观察到的OH通常为模型OH的0.95。在8 km以下,观察到的HO2通常是模型HO2的1.20。这种观察到模型的比较类似于TRACE-P,这是另一项中纬度研究,该研究的中位观察到模型比率为OH为1.08,HO2为1.34,而PEM-TB为热带研究。 OH的中位数观察模型与模型比率为1.17,HO2的中位数观察模型与模型比率为0.97。 8 km以上的HO2行为明显不同。观测到的模型化的HO2比从8 km处的〜1.2增加到11 km处的〜3,与NO的相关。在8公里以上,观测到的模型HO2和观测到的NO均明显大于先前活动的观测结果。另外,对OH和HO2之间的循环反应敏感的观察到的模型HO2 / OH从8 km处的〜1.5增加到11 km处的近3.5。这些差异表明存在大量未知的HO x源,以及使HO x从OH循环到HO2的其他反应物。在大陆行星边界层,观测到的模拟OH比值从异戊二烯小于0.1 ppbv时的1增加到异戊二烯大于2 ppbv时的4以上,这表明美国各地的森林正在散发未知的HO x来源。为了解决这些差异,需要开展一项重点研究活动,以进一步检查可能的未知OH吸收剂和HO x来源。

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