Das Sourav, Prospero Joseph M, Chellam Shankararaman
Zachry Department of Civil & Environmental Engineering, Texas A&M University, College Station, TX, 77843, USA.
Rosenstiel School of Marine and Atmospheric Science, University of Miami, Miami, FL, USA.
Atmos Environ (1994). 2023 Jan 1;292. doi: 10.1016/j.atmosenv.2022.119415.
We quantify the contributions of long-range and regionally transported aerosols to ambient primary PM and PM in a representative United States industrialized/urban atmosphere via detailed elemental analysis and chemical mass balance (CMB) modeling after identifying their presence using a variety of publicly available satellite data/information, software products, and synoptic-scale aerosol models. A year-long study in Houston, Texas identified North African dust as the principal long-range global source of primary particulate matter (PM). CMB estimated transatlantic dust from the Sahara-Sahel region to be dominant in the summer months contributing an average of 3.5 μg m to PM and 7.9 μg m to PM during May-August, i.e., the active Saharan dust season. Biomass burning was the chief source of regionally transported PM impacting air quality on different occasions throughout the year depending on the fire location. Four major biomass combustion events affecting air quality in Texas were calculated to contribute an average of 1.3 μg m to PM and 1.4 μg m to PM in corresponding samples whose origins were tracked to Canada, southeastern states of USA, and Central America using fire maps, HYSPLIT back trajectories, and the Navy Aerosol Analysis and Prediction System global aerosol model. Elemental concentrations and signature ratios revealed significant mixing of potassium, rare earth metals, and vanadium from proximal and distal crustal (natural) sources with anthropogenically emitted PM. This demonstrates the need to isolate the non-mineral components of these metals to employ them as tracers for primary PM emitted by biomass burning, petroleum refineries, and oil combustion. Transboundary contributions to primary PM were 1.5 μg m and 3.1 μg m to PM adding 16% to annual average mass concentration of both size fractions demonstrating that local sources were primarily responsible for ambient air quality with non-trivial contributions from international and interstate sources. Rigorously identifying and quantifying aerosol sources assists in improving air quality management policies designed to protect public health and comply with ever-decreasing federal PM standards that allow state agencies to exclude contributions that are not reasonably controllable or preventable from regulatory decisions and actions.
在利用各种公开的卫星数据/信息、软件产品和天气尺度气溶胶模型确定远程和区域传输气溶胶的存在后,我们通过详细的元素分析和化学质量平衡(CMB)模型,量化了在美国典型工业化/城市大气中,远程和区域传输气溶胶对环境一次颗粒物(PM)和PM的贡献。在得克萨斯州休斯顿进行的为期一年的研究确定,北非沙尘是一次颗粒物(PM)的主要远程全球来源。CMB估计,来自撒哈拉 - 萨赫勒地区的跨大西洋沙尘在夏季占主导地位,在5月至8月(即活跃的撒哈拉沙尘季节),平均对PM贡献3.5 μg/m ,对PM贡献7.9 μg/m 。生物质燃烧是全年不同时段影响空气质量的区域传输PM的主要来源,这取决于火灾发生地点。利用火灾地图、HYSPLIT反向轨迹和海军气溶胶分析与预测系统全球气溶胶模型,计算出影响得克萨斯州空气质量的四次主要生物质燃烧事件,在相应样本中平均对PM贡献1.3 μg/m ,对PM贡献1.4 μg/m ,其来源追踪到加拿大、美国东南部各州和中美洲。元素浓度和特征比率表明,来自近端和远端地壳(自然)源的钾、稀土金属和钒与人为排放的PM有显著混合。这表明需要分离这些金属的非矿物成分,以便将它们用作生物质燃烧、石油炼制和石油燃烧排放的一次PM的示踪剂。对一次PM 的跨境贡献分别为1.5 μg/m 和3.1 μg/m ,占两个粒径分数年平均质量浓度的16%,这表明本地源是环境空气质量的主要原因,国际和州际源也有重要贡献。严格识别和量化气溶胶来源有助于改进旨在保护公众健康并符合不断降低的联邦PM标准的空气质量管理政策,这些标准允许州机构在监管决策和行动中排除那些无法合理控制或预防的贡献。