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Temporal and spatial variability of atmospheric particle number size distributions across Spain

机译:西班牙大气颗粒数大小分布的时空变化

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摘要

This study synthesizes for the first time results from simultaneous aerosol measurements performed at seven diverse locations distributed all over the Spanish geography. The observations were carried out during two field campaigns in 2012-2013, one-month each and during different seasons. These field campaigns were performed in the framework of the Spanish Network of DMAs (REDMAAS) activities. Measurement sites were grouped as polluted sites (urban background) and clean sites (rural background and high-altitude sites). Seasonal differences were more important at polluted sites, mainly related to meteorology and aerosol sources. Higher total particle concentrations were found during the cold period, driven mainly by Aitken-mode particles (traffic-related aerosol particles). In clean sites, particle concentrations were higher during the warm period. Mild meteorological conditions in combination with the absence of local sources during the cold period make atmospheric nucleation an important contributor to ultrafine particles. These results are reflected in aerosol dynamical processes. Ultrafine particle bursts were frequent in both periods at the clean sites and in the warm period at most polluted sites. Shrinkages processes were identified at three sites (two polluted and one clean site) during the warm period. Meteorology (wind speed and solar radiation) and a highly-volatile aerosol (formed from atmospheric nucleation or traffic emissions) explain this behaviour. Ultrafine particles exhibited a different behaviour at inland and coastal sites. The highest total particle concentrations were observed at coastal sites during the warm period. At these sites, the smallest particle modal diameters and the highest variations of particle number size distributions in the smaller particle size range were also found, particularly in the warm period. This may be the result of the high diffusion conditions and mixing of different air masses (clean and polluted) caused by sea-land breezes. Our findings can be explained by the local and regional characteristics of each site, such as meteorology and aerosol sources (types, proximity ...) and the influence of meteorology on atmospheric transformation processes.
机译:这项研究首次综合了在整个西班牙地理分布的七个不同地点同时进行的气溶胶测量结果。这些观测是在2012-2013年的两次野外运动中进行的,每次运动为一个月,在不同的季节进行。这些实地运动是在西班牙DMA网络(REDMAAS)活动的框架内进行的。测量地点分为污染地点(城市背景)和干净地点(农村背景和高海拔地点)。在受污染的地点,季节性差异更为重要,这主要与气象学和气溶胶来源有关。在寒冷时期发现了较高的总颗粒浓度,这主要是由Aitken模式颗粒(交通相关的气溶胶颗粒)驱动的。在干净的地方,在温暖的时期颗粒浓度较高。寒冷时期的温和气象条件加上缺乏本地资源,使大气成核成为超细颗粒的重要贡献者。这些结果反映在气溶胶动力学过程中。在清洁地点和大多数污染地点的温暖时期,超细颗粒爆裂都频繁发生。在温暖时期,在三个地点(两个被污染的地点和一个干净的地点)发现了收缩过程。气象(风速和太阳辐射)和高挥发性气溶胶(由大气成核或交通排放形成)解释了这种行为。超细颗粒在内陆和沿海地区表现出不同的行为。在温暖时期,在沿海地区观测到最高的总颗粒浓度。在这些位置,还发现在较小的粒径范围内,尤其是在暖期,粒径模态直径最小,粒径分布的最大变化。这可能是由于海陆微风引起的高扩散条件和不同空气质量(干净和污染)混合的结果。我们的发现可以用每个站点的本地和区域特征来解释,例如气象和气溶胶源(类型,邻近度...)以及气象对大气转换过程的影响。

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