Chow Judith C, Watson John G, Lowenthal Douglas H, Hackney Richard, Magliano Karen, Lehrman Donald, Smith Ted
a Desert Research Institute , Reno , Nevada , USA.
b California Air Resources Board , Sacramento , California , USA.
J Air Waste Manag Assoc. 1999 Sep;49(9):16-24. doi: 10.1080/10473289.1999.10463909.
The spatial and temporal distributions of particle mass and its chemical constituents are essential for understanding the source-receptor relationships as well as the chemical, physical, and meteorological processes that result in elevated particulate concentrations in California's San Joaquin Valley (SJV). Fine particulate matter PM coarse particulate matter (PM), and aerosol precursor gases were sampled on a 3-hr time base at two urban (Bakersfield and Fresno) and two non-urban (Kern Wildlife Refuge and Chowchilla) core sites in the SJV during the winter of 1995-1996. Day-to-day variations of PM and PM and their chemical constituents were influenced by the synoptic-scale meteorology and were coherent among the four core sites. Under non-rainy conditions, similar diurnal variations of PM and coarse aerosol were found at the two urban sites, with concentrations peaking during the nighttime hours. Conversely, PM and coarse aerosol peaked during the morning and afternoon hours at the two non-urban sites. Under rainy and foggy conditions, these diurnal patterns were absent or greatly suppressed. In the urban areas, elevated concentrations of primary pollutants (e.g., organic and elemental carbons) during the late afternoon and nighttime hours reflected the impact from residential wood combustion and motor vehicle exhaust. During the daytime, these concentrations decreased as the mixed layer deepened. Increases of secondary nitrate and sulfate concentrations were found during the daylight hours as a result of photochemical reactions. At the non-urban sites, the same increases in secondary aerosol concentrations occurred during the daylight hours but with a discernable lag time. Concentrations of the primary pollutants also increased at the non-urban sites during the daytime. These observations are attributed to mixing aloft of primary aerosols and secondary precursor gases in urban areas followed by rapid transport aloft to non-urban areas coupled with photochemical conversion.
颗粒物质量及其化学成分的时空分布对于理解源 - 受体关系以及导致加利福尼亚州圣华金谷(SJV)颗粒物浓度升高的化学、物理和气象过程至关重要。在1995 - 1996年冬季,在SJV的两个城市核心站点(贝克斯菲尔德和弗雷斯诺)以及两个非城市核心站点(克恩野生动物保护区和乔奇拉),以3小时为时间间隔对细颗粒物(PM)、粗颗粒物(PM)和气溶胶前体气体进行了采样。PM和PM及其化学成分的逐日变化受天气尺度气象学影响,并且在四个核心站点之间具有一致性。在非降雨条件下,两个城市站点的PM和粗气溶胶呈现相似的日变化,浓度在夜间达到峰值。相反,两个非城市站点的PM和粗气溶胶在上午和下午达到峰值。在降雨和有雾条件下,这些日变化模式不存在或被极大抑制。在城市地区,傍晚和夜间主要污染物(如有机碳和元素碳)浓度升高反映了居民燃木和机动车尾气的影响。在白天,随着混合层加深,这些浓度降低。由于光化学反应,白天发现二次硝酸盐和硫酸盐浓度增加。在非城市站点,白天二次气溶胶浓度也出现同样的增加,但有明显的滞后时间。白天非城市站点的主要污染物浓度也有所增加。这些观测结果归因于城市地区主要气溶胶和二次前体气体在高空混合,随后迅速向非城市地区高空输送并伴随光化学转化。