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首页> 外文期刊>The Science of the Total Environment >Sources of pollution and interrelationships between aerosol and precipitation chemistry at a central California site
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Sources of pollution and interrelationships between aerosol and precipitation chemistry at a central California site

机译:加利福尼亚中部站点的污染源以及气溶胶与降水化学之间的相互关系

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This study examines co-located aerosol and precipitation chemistry data between 2010 and 2016 at Pinnacles National Monument -65 km east of the coastline in central California. Positive matrix factorization analysis of the aerosol composition data revealed seven distinct pollutant sources: aged sea salt (25.7% of PM2.5), biomass burning (24.2% of PM2.5), fresh sea salt (15.0% of PM2.5), secondary sulfate (11.7% of PM2.5), dust (10.0% of PM2.5), vehicle emissions (8.2% of PM2.5), and secondary nitrate (5.2% of PM2.5). The influence of meteorology and transport on monthly patterns of PM2.5 composition is discussed. Only secondary sulfate exhibited a statistically significant change (a reduction) over time among the PM2.5 source factors. In contrast, PMcoarse exhibited a significant increase most likely due to dust influence. Monthly profiles of precipitation chemistry are summarized showing that the most abundant species in eachmonthwas either SO42-, NO3-, or Cl-. Intercomparisons between the precipitation and aerosol data revealed several features: (i) precipitation pH was inversely related to factors associatedwith more acidic aerosol constituents such as secondary sulfate and aged sea salt, in addition to being reduced by uptake of HNO3 in the liquid phase; (ii) two aerosol source factors (dust and aged sea salt) and PMcoarse exhibited a positive association with Ca2+ in precipitation, suggestive of directly emitted aerosol types with larger sizes promoting precipitation; and (iii) sulfate levels in both the aerosol and precipitation samples analyzed were significantly correlated with dust and aged sea salt PMF factors, pointing to the partitioning of secondary sulfate to dust and sea salt particles. The results of this work have implications for the region's air quality and hydrological cycle, in addition to demonstrating that the use of co-located aerosol and precipitation chemistry data can provide insights relevant to aerosol-precipitation interactions. (C) 2018 Elsevier B.V. All rights reserved.
机译:这项研究调查了2010年至2016年期间位于加利福尼亚中部海岸线以东65公里处的Pinnacles国家纪念碑的同一位置的气溶胶和降水化学数据。对气溶胶成分数据进行的正矩阵分解分析显示了七种不同的污染物来源:陈年海盐(占PM2.5的25.7%),生物质燃烧(占PM2.5的24.2%),新鲜海盐(占PM2.5的15.0%),次级硫酸盐(占PM2.5的11.7%),粉尘(占PM2.5的10.0%),车辆排放物(占PM2.5的8.2%)和硝酸盐(占PM2.5的5.2%)。讨论了气象和运输对PM2.5组成每月模式的影响。在PM2.5来源因素中,只有仲硫酸盐随时间显示出统计学上的显着变化(减少)。相反,PMcoarse最有可能由于粉尘影响而显示出明显的增加。总结了降水化学的月度分布图,显示每个月最丰富的物种是SO42-,NO3-或Cl-。降水和气溶胶数据之间的比较显示了几个特征:(i)降水的pH与更多酸性酸性气溶胶成分(例如二次硫酸盐和老化的海盐)相关的因素成反比,此外还因为液相中HNO3的吸收而降低; (ii)两种气溶胶源因子(粉尘和老化的海盐)和PMcoarse与降水中的Ca2 +呈正相关,暗示直接排放的较大气溶胶类型促进了降水; (iii)所分析的气溶胶和降水样品中的硫酸盐含量均与粉尘和老化的海盐PMF因子显着相关,表明次级硫酸盐在粉尘和海盐颗粒中的分配。这项工作的结果除了表明使用同一位置的气溶胶和降水化学数据可以提供与气溶胶-降水相互作用有关的见解之外,还对该地区的空气质量和水文循环产生了影响。 (C)2018 Elsevier B.V.保留所有权利。

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