Chemical Evolution of Biomass Burning Aerosols across Wildfire Plumes in the Western U.S.: From Near-Source to Regional Scales

Ryan Farley, Shan Zhou, Sonya Collier, Wenqing Jiang, Timothy B. Onasch, John E. Shilling, Lawrence Kleinman, Arthur J. Sedlacek III and Qi Zhang*, 
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Abstract

The atmospheric processing of biomass burning organic aerosol (BBOA) and its implications for tropospheric aerosol physicochemical properties remain uncertain. To address this gap, we investigate the chemical transformation of BBOA from wildfire events in the western U.S., using data from aerosol mass spectrometers aboard the DOE G-1 aircraft and at the Mt. Bachelor Observatory (∼2800 m a.s.l.) during the summers of 2013 and 2019. This study captures dynamic changes in submicron particulate matter (PM1) concentrations and chemical profiles within wildfire plumes that span a broad range of atmospheric ages, from fresh emissions (<30 min) to plumes transported for several days. As plumes age, the oxidation state of organic aerosols (OA) increases, accompanied by the formation of secondary aerosol components such as phenolic secondary OA (SOA) species, carboxylic acids, and potassium sulfate. Early plume evolution is marked by the evaporation of semivolatile components and the formation of alcohol and peroxide functional groups, while extended aging produces more oxidized species, including carboxylic acids and carbonyl compounds. Normalized excess mixing ratios (NEMRs) of OA to CO demonstrate a complex interplay between evaporation, SOA formation, and oxidative loss. Using positive matrix factorization (PMF), we identify distinct BBOA types representing various stages of atmospheric processing and assess the contributions of primary BBOA and secondary BBOA formed through atmospheric reactions. These findings shed light on the intricate mechanisms governing the evolution of BBOA characteristics within wildfire plumes, providing critical insights to improve atmospheric modeling of BBOA and better assess the environmental and climatic impacts of wildfire emissions.

This study integrates aircraft and mountaintop observatory measurements of wildfire emissions to analyze the chemical characteristics of aerosols and their transformation processes across a wide range of atmospheric ages.

美国西部野火羽流中生物质燃烧气溶胶的化学演化:从近源到区域尺度
生物质燃烧有机气溶胶(BBOA)的大气处理过程及其对对流层气溶胶物理化学特性的影响仍不确定。为了填补这一空白,我们利用 2013 年和 2019 年夏季 DOE G-1 飞机上的气溶胶质谱仪和学士山天文台(海拔 ∼ 2800 米)的数据,研究了美国西部野火事件产生的生物质燃烧有机气溶胶的化学转化。这项研究捕捉了野火羽流中亚微米颗粒物(PM1)浓度和化学剖面的动态变化,这些变化跨越了广泛的大气年龄范围,从新鲜排放(30 分钟)到飘移数天的羽流。随着烟羽年龄的增长,有机气溶胶(OA)的氧化态增加,并伴随着酚类二次 OA(SOA)物种、羧酸和硫酸钾等二次气溶胶成分的形成。早期羽流演变的特点是半挥发性成分的蒸发以及醇和过氧化物官能团的形成,而长时间的老化则会产生更多的氧化物,包括羧酸和羰基化合物。OA 与 CO 的归一化过量混合比(NEMRs)显示了蒸发、SOA 形成和氧化损失之间复杂的相互作用。利用正矩阵因式分解(PMF),我们确定了代表大气处理过程各个阶段的不同的BBOA类型,并评估了一次BBOA和通过大气反应形成的二次BBOA的贡献。这些发现揭示了野火羽流中 BBOA 特性演变的复杂机制,为改进 BBOA 的大气建模和更好地评估野火排放对环境和气候的影响提供了重要的见解。这项研究综合了飞机和山顶观测站对野火排放的测量结果,分析了气溶胶的化学特性及其在各种大气年龄段的转化过程。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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