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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:加利福尼亚州气溶胶和降水化学之间的污染源和相互关系

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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:本研究审查了2010年至2016年在2010年至2016年间的共同定位的气溶胶和降水化学数据 - 在加利福尼亚州中部海岸线东部65公里处。气溶胶组成数据的阳性基质分解分析显示出七种不同的污染物来源:老年海盐(占PM2.5的25.7%),生物量燃烧(24.2%的PM2.5),新鲜海盐(15.0%的PM2.5),二级硫酸盐(11.7%的PM2.5),灰尘(PM2.5的10%),载体排放(PM2.5的8.2%)和仲硝酸盐(5.2%的PM2.5)。讨论了气象学和运输对PM2.5组成的月度模式的影响。在PM2.5源极端因子中,次级硫酸盐仅在统计上显着的变化(减少)。相比之下,PMCOASSASS呈现出显着的增加,最有可能因粉尘影响而产生。总结了降水化学的月度概况表明每种MONSWAS中最丰富的物种为SO42-,NO3-或CL-。沉淀和气溶胶数据之间的离法显示出几种特征:(i)沉淀pH与与酸性气溶胶成分如仲硫酸盐和老化的海盐等因素反向相关,除了在液相中的HNO3摄取的影响之外,还具有降低; (ii)两个气溶胶源极端因素(灰尘和老化的海盐)和PMCoarse表现出与Ca2 +在降水中的阳性关联,暗示直接发出的气溶胶类型,促进沉淀的较大尺寸; (III)分析的气溶胶和沉淀样品中的硫酸盐水平与粉尘和老化的海盐PMF因子显着相关,指向仲硫酸盐与灰尘和海盐颗粒的分配。这项工作的结果对该地区的空气质量和水文循环具有影响,除了证明使用共同定位的气溶胶和降水化学数据,可以提供与气溶胶沉淀相互作用相关的见解。 (c)2018年elestvier b.v.保留所有权利。

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