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Mixing of Asian dust with pollution aerosol and the transformation of aerosol components during the dust storm over China in spring 2007

机译:2007年春季中国沙尘暴期间亚洲粉尘与污染气溶胶的混合以及气溶胶成分的变化

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摘要

An intensive spring aerosol sampling campaign over northwestern and northern China and a megacity in eastern China was conducted in the spring of 2007 to investigate the mixing of Asian dust with pollution aerosol during its long-range transport. On the basis of the results of the three sites near dust source regions (Tazhong, Yulin, and Duolun) and a metropolitan city (Shanghai), three dust sources, i.e., the western high-Ca dust in the Taklimakan Desert, the northwestern high-Ca dust and the northeastern low-Ca dust in Mongolia Gobi, were identified on the basis of the air mass trajectories and the elemental tracer analysis (e.g., Ca/Al, SO_4~(2-)/S, Ca~(2+)/Ca, and Na~+/Na). The western dust was least polluted in comparison to the other two dust sources. The results evidently indicated that the dust could have already mixed with pollution aerosol even in near dust source regions. The concentrations of As, Cd, Cu, Pb, Zn, and S were elevated several times at all sites during dust days, showing the entrainment of pollution elements by dust. The secondary SO_4~(2-) was observed to show much higher concentration due to the heterogeneous reaction on the alkaline dust during dust storm, while the concentrations of NO_3~- and NH_4~+ decreased owing to the dilution of the local pollution by the invaded dust. The western dust contained relatively low anthropogenic aerosols, and it mainly derived from the Taklimakan Desert, a paleomarine source. The northwestern dust had a considerable chemical reactivity and mixing with sulfur precursors emitted from the coal mines on the pathway of the long-range transport of dust. The northeastern dust reached Shanghai with high acidity, and it became the mixed aerosol with the interaction among dust, local pollutants, and sea salts. Comparison of the speciation of the water-soluble ions on both nondust and dust days at all sites illustrated the evolution of major ion species from different dust sources during the long-range transport of dust. The mixing mechanisms of the dust with the pollution aerosol on the local, medium-range, and long-range scale revealed from this study would improve the understanding of the impacts of Asian dust on the regional/global climate change.
机译:2007年春季,在中国西北和北部以及中国东部的一个特大城市进行了一次密集的春季气溶胶采样活动,以调查亚洲粉尘与污染气溶胶在远程运输过程中的混合情况。根据尘埃源区(塔中,榆林和多伦)和大都市(上海)附近三个站点的结果,三个尘埃源,即塔克拉玛干沙漠中的西部高钙尘,西北高处。根据空气轨迹和元素示踪分析(如Ca / Al,SO_4〜(2-)/ S,Ca〜(2+),确定了蒙古戈壁地区的-Ca尘埃和东北低Ca尘埃)/ Ca,和Na〜+ / Na)。与其他两个粉尘源相比,西部粉尘污染最少。结果显然表明,即使在粉尘源附近,粉尘也可能已经与污染气溶胶混合。在粉尘天期间,所有地点的As,Cd,Cu,Pb,Zn和S的浓度均升高了数倍,显示出粉尘夹带了污染元素。由于沙尘暴期间碱性尘埃的异质反应,导致次生SO_4〜(2-)的浓度高得多,而NO_3〜-和NH_4〜+的浓度则由于局部污染被稀释而降低。侵入的灰尘。西部尘埃含有较低的人为气溶胶,主要来自古马林源塔克拉玛干沙漠。西北粉尘具有相当大的化学反应性,并与粉尘的长距离传输路径上的煤矿排放的硫前体混合。东北尘埃以高酸度到达上海,成为尘埃,当地污染物和海盐之间相互作用的混合气溶胶。在所有地点的无尘天和粉尘天的水溶性离子形态的比较表明,在粉尘的远距离迁移过程中,来自不同粉尘源的主要离子物种的演变。这项研究揭示了尘埃与污染气溶胶在局部,中距离和远距离尺度上的混合机理,将有助于人们更好地了解亚洲尘埃对区域/全球气候变化的影响。

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