O'Neill Susan M, Lamb Brian K, Chen Jack, Claiborn Candis, Finn Dennis, Otterson Sally, Figueroa Cristiana, Bowman Clint, Boyer Mike, Wilson Rob, Arnold Jeff, Aalbers Steven, Stocum Jeffrey, Swab Christopher, Stoll Matt, Dubois Mike, Anderson Mary
Pacific Wildland Fire Sciences Laboratory, U.S. Department of Agriculture Forest Service, 400 North 34th Street, Suite 201, Seattle, Washington 98103, USA.
Environ Sci Technol. 2006 Feb 15;40(4):1286-99. doi: 10.1021/es048402k.
The Community Multi-Scale Air Quality (CMAQ) modeling system was used to investigate ozone and aerosol concentrations in the Pacific Northwest (PNW) during hot summertime conditions during July 1-15, 1996. Two emission inventories (El) were developed: emissions for the first El were based upon the National Emission Trend 1996 (NET96) database and the BEIS2 biogenic emission model, and emissions for the second El were developed through a "bottom up" approach that included biogenic emissions obtained from the GLOBEIS model. The two simulations showed that elevated PM2.5 concentrations occurred near and downwind of the Interstate-5 corridor along the foothills of the Cascade Mountains and in forested areas of central Idaho. The relative contributions of organic and inorganic aerosols varied by region, but generally organic aerosols constituted the largest fraction of PM2.5. In wilderness areas near the 1-5 corridor, organic carbon from anthropogenic sources contributed approximately 50% of the total organic carbon with the remainder from biogenic precursors, while in wilderness areas in Idaho, biogenic organic carbon accounted for 80% of the total organic aerosol. Regional analysis of the secondary organic aerosol formation in the Columbia River Gorge, Central Idaho, and the Olympics/Puget Sound showed that the production rate of secondary organic carbon depends on local terpene concentrations and the local oxidizing capacity of the atmosphere, which was strongly influenced by anthropogenic emissions. Comparison with observations from 12 IMPROVE sites and 21 ozone monitoring sites showed that results from the two El simulations generally bracketed the average observed PM parameters and that errors calculated for the model results were within acceptable bounds. Analysis across all statistical parameters indicated that the NW-AIRQUEST El solution performed better at predicting PM2.5, PM1, and beta(ext) even though organic carbon PM was over-predicted, and the NET96 El solution performed better with regard to the inorganic aerosols. For the NW-AIRQUEST El solution, the normalized bias was 30% and the normalized absolute error was 49% for PM2.5 mass. The NW-AIRQUEST solution slightly overestimated peak hourly ozone downwind of urban areas, while the NET96 solution slightly underestimated peak values, and both solutions over-predicted average 03 concentrations across the domain by approximately 6 ppb.
利用社区多尺度空气质量(CMAQ)建模系统,对1996年7月1日至15日炎热夏季期间太平洋西北地区(PNW)的臭氧和气溶胶浓度进行了调查。开发了两种排放清单(EI):第一个EI的排放基于1996年国家排放趋势(NET96)数据库和BEIS2生物源排放模型,第二个EI的排放通过“自下而上”的方法得出,该方法包括从GLOBEIS模型获得的生物源排放。这两个模拟结果表明,沿喀斯喀特山脉山麓的5号州际公路走廊附近及下风处以及爱达荷州中部的森林地区,PM2.5浓度升高。有机气溶胶和无机气溶胶的相对贡献因地区而异,但一般来说,有机气溶胶在PM2.5中占最大比例。在5号州际公路走廊附近的荒野地区,人为源有机碳约占总有机碳的50%,其余来自生物源前体,而在爱达荷州的荒野地区,生物源有机碳占总有机气溶胶的80%。对哥伦比亚河峡谷、爱达荷州中部以及奥林匹克/普吉特海湾二次有机气溶胶形成的区域分析表明,二次有机碳的生成速率取决于当地萜烯浓度和当地大气氧化能力,而这受到人为排放的强烈影响。与12个IMPROVE站点和21个臭氧监测站点的观测结果比较表明,两个EI模拟结果通常涵盖了观测到的PM参数平均值,并且模型结果计算出的误差在可接受范围内。对所有统计参数的分析表明,尽管有机碳PM被高估,但NW - AIRQUEST EI解决方案在预测PM2.5、PM1和β(ext)方面表现更好,而NET96 EI解决方案在无机气溶胶方面表现更好。对于NW - AIRQUEST EI解决方案,PM2.5质量的归一化偏差为30%,归一化绝对误差为49%。NW - AIRQUEST解决方案略微高估了城市下风处的每小时臭氧峰值,而NET96解决方案略微低估了峰值,并且两种解决方案都将整个区域的平均臭氧浓度高估了约6 ppb。