Xu Lu, Pye Havala O T, He Jia, Chen Yunle, Murphy Benjamin N, Ng Lee Nga
School of Chemical and Biomolecular Engineering, Georgia Institute of Technology, Atlanta, GA 30332, USA.
National Exposure Research Laboratory, US Environmental Protection Agency, Research Triangle Park, NC 27711, USA.
Atmos Chem Phys. 2018;18(17):12613-12637. doi: 10.5194/acp-18-12613-2018. Epub 2018 Aug 31.
Atmospheric organic aerosol (OA) has important impacts on climate and human health but its sources remain poorly understood. Biogenic monoterpenes and sesquiterpenes are important precursors of secondary organic aerosol (SOA), but the amounts and pathways of SOA generation from these precursors are not well constrained by observations. We propose that the less-oxidized oxygenated organic aerosol (LO-OOA) factor resolved from positive matrix factorization (PMF) analysis on aerosol mass spectrometry (AMS) data can be used as a surrogate for fresh SOA from monoterpenes and sesquiterpenes in the southeastern US. This hypothesis is supported by multiple lines of evidence, including lab-in-the-field perturbation experiments, extensive ambient ground-level measurements, and state-of-the-art modeling. We performed lab-in-the-field experiments in which the ambient air is perturbed by the injection of selected monoterpenes and sesquiterpenes, and the subsequent SOA formation is investigated. PMF analysis on the perturbation experiments provides an objective link between LO-OOA and fresh SOA from monoterpenes and sesquiterpenes as well as insights into the sources of other OA factors. Further, we use an upgraded atmospheric model and show that modeled SOA concentrations from monoterpenes and sesquiterpenes could reproduce both the magnitude and diurnal variation of LO-OOA at multiple sites in the southeastern US, building confidence in our hypothesis. We estimate the annual average concentration of SOA from monoterpenes and sesquiterpenes in the southeastern US to be roughly 2 μg m.
大气有机气溶胶(OA)对气候和人类健康有着重要影响,但其来源仍知之甚少。生物源单萜和倍半萜是二次有机气溶胶(SOA)的重要前体,但这些前体生成SOA的量和途径尚未得到观测的充分约束。我们提出,通过对气溶胶质谱(AMS)数据进行正矩阵因子分解(PMF)分析解析出的氧化程度较低的含氧有机气溶胶(LO-OOA)因子,可作为美国东南部单萜和倍半萜产生的新鲜SOA的替代物。这一假设得到了多方面证据的支持,包括野外现场扰动实验、广泛的环境地面测量以及最先进的模型。我们进行了野外现场实验,通过注入选定的单萜和倍半萜来扰动环境空气,并研究随后的SOA形成。对扰动实验进行的PMF分析提供了LO-OOA与单萜和倍半萜产生的新鲜SOA之间的客观联系,以及对其他OA因子来源的深入了解。此外,我们使用了升级后的大气模型,并表明单萜和倍半萜模拟的SOA浓度能够再现美国东南部多个地点LO-OOA的量级和日变化,从而增强了我们对这一假设的信心。我们估计美国东南部单萜和倍半萜产生的SOA的年平均浓度约为2μg/m³。