Pitchford Marc L, Schichtel Bret A, Gebhart Kristi A, Barna Michael G, Malm William C, Tombach Ivar H, Knipping Eladio M
National Oceanic and Atmospheric Administration, Air Resources Laboratory, Las Vegas, NV 89119-7363, USA.
J Air Waste Manag Assoc. 2005 Nov;55(11):1726-32. doi: 10.1080/10473289.2005.10464766.
The recently completed Big Bend Regional Aerosol and Visibility Observational (BRAVO) Study focused on particulate sulfate source attribution for a 4-month period from July through October 1999. A companion paper in this issue by Schichtel et al. describes the methods evaluation and results reconciliation of the BRAVO Study sulfate attribution approaches. This paper summarizes the BRAVO Study extinction budget assessment and interprets the attribution results in the context of annual and multiyear causes of haze by drawing on long-term aerosol monitoring data and regional transport climatology, as well as results from other investigations. Particulate sulfates, organic carbon, and coarse mass are responsible for most of the haze at Big Bend National Park, whereas fine particles composed of light-absorbing carbon, fine soils, and nitrates are relatively minor contributors. Spring and late summer through fall are the two periods of high-haze levels at Big Bend. Particulate sulfate and carbonaceous compounds contribute in a similar magnitude to the spring haze period, whereas sulfates are the primary cause of haze during the late summer and fall period. Atmospheric transport patterns to Big Bend vary throughout the year, resulting in a seasonal cycle of different upwind source regions contributing to its haze levels. Important sources and source regions for haze at Big Bend include biomass smoke from Mexico and Central America in the spring and African dust during the summer. Sources of sulfur dioxide (SO2) emissions in Mexico, Texas, and in the Eastern United States all contribute to Big Bend haze in varying amounts over different times of the year, with a higher contribution from Mexican sources in the spring and early summer, and a higher contribution from U.S. sources during late summer and fall. Some multiple-day haze episodes result from the influence of several source regions, whereas others are primarily because of emissions from a single source region.
最近完成的大弯地区气溶胶与能见度观测(BRAVO)研究聚焦于1999年7月至10月这4个月期间颗粒硫酸盐的来源归因。Schichtel等人在本期发表的一篇配套论文描述了BRAVO研究中硫酸盐归因方法的评估及结果核对。本文总结了BRAVO研究的消光预算评估,并借助长期气溶胶监测数据、区域传输气候学以及其他调查结果,在年度和多年雾霾成因的背景下解读归因结果。颗粒硫酸盐、有机碳和粗颗粒物是大弯国家公园大部分雾霾的成因,而由吸光碳、细土壤和硝酸盐组成的细颗粒物贡献相对较小。春季以及夏末至秋季是大弯地区雾霾水平较高的两个时期。颗粒硫酸盐和含碳化合物对春季雾霾期的贡献程度相近,而硫酸盐是夏末和秋季雾霾的主要成因。全年输送至大弯地区的大气环流模式各不相同,导致不同上风源区对其雾霾水平的贡献呈现季节性循环。大弯地区雾霾的重要来源和源区包括春季来自墨西哥和中美洲的生物质烟雾以及夏季的非洲沙尘。墨西哥、得克萨斯州和美国东部的二氧化硫(SO₂)排放源在一年中的不同时间对大弯地区的雾霾均有不同程度的贡献,春季和初夏时墨西哥排放源的贡献较大,夏末和秋季时美国排放源的贡献较大。一些持续多日的雾霾事件是由多个源区的影响导致的,而其他一些则主要是由单个源区的排放造成的。