Chakrabarty Rajan K, Shetty Nishit J, Thind Arashdeep S, Beeler Payton, Sumlin Benjamin J, Zhang Chenchong, Liu Pai, Idrobo Juan C, Adachi Kouji, Wagner Nicholas L, Schwarz Joshua P, Ahern Adam, Sedlacek Arthur J, Lambe Andrew, Daube Conner, Lyu Ming, Liu Chao, Herndon Scott, Onasch Timothy B, Mishra Rohan
Center for Aerosol Science and Engineering, Department of Energy, Environmental, and Chemical Engineering, Washington University in St Louis, St Louis, MO USA.
Institute of Materials Science and Engineering, Washington University in St Louis, St Louis, MO USA.
Nat Geosci. 2023;16(8):683-688. doi: 10.1038/s41561-023-01237-9. Epub 2023 Aug 7.
Wildfires emit large amounts of black carbon and light-absorbing organic carbon, known as brown carbon, into the atmosphere. These particles perturb Earth's radiation budget through absorption of incoming shortwave radiation. It is generally thought that brown carbon loses its absorptivity after emission in the atmosphere due to sunlight-driven photochemical bleaching. Consequently, the atmospheric warming effect exerted by brown carbon remains highly variable and poorly represented in climate models compared with that of the relatively nonreactive black carbon. Given that wildfires are predicted to increase globally in the coming decades, it is increasingly important to quantify these radiative impacts. Here we present measurements of ensemble-scale and particle-scale shortwave absorption in smoke plumes from wildfires in the western United States. We find that a type of dark brown carbon contributes three-quarters of the short visible light absorption and half of the long visible light absorption. This strongly absorbing organic aerosol species is water insoluble, resists daytime photobleaching and increases in absorptivity with night-time atmospheric processing. Our findings suggest that parameterizations of brown carbon in climate models need to be revised to improve the estimation of smoke aerosol radiative forcing and associated warming.
野火会向大气中释放大量黑碳以及吸光有机碳(即棕碳)。这些颗粒通过吸收入射的短波辐射扰乱地球的辐射收支。一般认为,由于阳光驱动的光化学漂白作用,棕碳在大气中排放后会失去其吸光性。因此,与相对惰性的黑碳相比,棕碳产生的大气变暖效应仍然高度可变,并且在气候模型中的表现较差。鉴于预计未来几十年全球野火将增加,量化这些辐射影响变得越来越重要。在此,我们展示了对美国西部野火烟雾羽流中整体尺度和颗粒尺度短波吸收的测量结果。我们发现,一种深棕色碳贡献了四分之三的短可见光吸收和一半的长可见光吸收。这种强吸收性有机气溶胶物质不溶于水,能抵抗白天的光漂白作用,并且随着夜间大气过程吸光性增强。我们的研究结果表明,需要修订气候模型中棕碳的参数化,以改进对烟雾气溶胶辐射强迫及相关变暖的估算。