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Organic trace gases of oceanic origin observed at South Pole during ISCAT 2000

机译:ISCAT 2000年在南极观测到的海洋有机痕量气体

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Volatile organic compounds (VOCs) were measured at the South Pole (SP) from late Austral spring to mid-summer 2000 as part of the Investigation of Sulfur Chemistry in the Antarctic Troposphere Program (ISCAT-2000). This paper focuses on VOCs that are directly emitted from the ocean, specifically dimethyl sulfide (DMS), methyl nitrate (CH3ONO2),. methyl iodide (CH3I) and bromoform (CHBr3). A partial seasonal cycle of these gases was also recorded during the year following ISCAT-2000. During he summer, the SP periodically receives relatively fresh marine air containing short-lived oceanic trace gases, such as DMS (iota approximate to 1 day). However, DMS was not detected at the SP until January even though DMS emissions from the Southern Ocean typically start peaking in November and elevated levels of other ocean-derived VOCs, including CH3ONO2 and CHBr3, were observed in mid-November. We speculate that in November and December most of the DMS is oxidized before it reaches the SP: a strong correlation between CH3ONO2 and methane sulfonate (MSA), an oxidation product of DMS, supports this hypothesis. Based on a limited number of samples taken over the course of one year, CH3ONO2 apparently accumulates to a quasi-steady-state level over the SP in winter, most likely due to continuing emissions of the compound coupled with a lower rate of photochemical destruction. Oceanic emissions were concluded to be the dominant source of alkyl nitrates at the SP; this is in sharp contrast to northern high latitudes where total alkyl nitrate mixing ratios are dominated by urban sources. (C) 2004 Elsevier Ltd. All rights reserved.
机译:作为南极对流层计划中硫化学研究的一部分(ISCAT-2000),从南极春季(春季)到2000年夏中期在南极(SP)测量了挥发性有机化合物(VOC)。本文重点研究直接从海洋排放的挥发性有机化合物,特别是二甲基硫(DMS),硝酸甲酯(CH3ONO2)。甲基碘(CH3I)和溴仿(CHBr3)。在ISCAT-2000之后的一年中,也记录了这些气体的部分季节性周期。在夏季,SP会定期接收相对新鲜的海洋空气,其中包含短寿命的海洋痕量气体,例如DMS(约1天的碘)。但是,直到南太平洋的DMS排放通常在11月开始达到峰值,并且在11月中旬观察到其他海洋衍生的VOC(包括CH3ONO2和CHBr3)的水平升高,SP才在1月才检测到DMS。我们推测,在11月和12月,大多数DMS在到达SP之前就已被氧化:CH3ONO2与DMS的氧化产物甲烷磺酸盐(MSA)之间的强相关性支持了这一假设。根据一年中采集的有限数量的样品,CH3ONO2显然在冬季整个SP积累到准稳态水平,最可能的原因是该化合物的持续排放以及较低的光化学破坏率。结论是,海洋排放是SP上硝酸烷基酯的主要来源。这与北方高纬度地区形成鲜明对比,后者的硝酸烷基酯总混合比主要由城市来源决定。 (C)2004 Elsevier Ltd.保留所有权利。

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