Global S&T Development Trend Analysis Platform of Resources and Environment
DOI | 10.5194/acp-19-7319-2019 |
Atmospheric evolution of molecular-weight-separated brown carbon from biomass burning | |
Wong, Jenny P. S.1; Tsagkaraki, Maria2; Tsiodra, Irini2,3; Mihalopoulos, Nikolaos2,4; Violaki, Kalliopi5; Kanakidou, Maria2; Sciare, Jean6; Nenes, Athanasios1,3,4,7; Weber, Rodney J.1 | |
2019-06-04 | |
发表期刊 | ATMOSPHERIC CHEMISTRY AND PHYSICS
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ISSN | 1680-7316 |
EISSN | 1680-7324 |
出版年 | 2019 |
卷号 | 19期号:11页码:7319-7334 |
文章类型 | Article |
语种 | 英语 |
国家 | USA; Greece; France; Cyprus; Switzerland |
英文摘要 | Biomass burning is a major source of atmospheric brown carbon (BrC), and through its absorption of UV/VIS radiation, it can play an important role in the planetary radiative balance and atmospheric photochemistry. The considerable uncertainty of BrC impacts is associated with its poorly constrained sources, transformations, and atmospheric lifetime. Here we report laboratory experiments that examined changes in the optical properties of the water-soluble (WS) BrC fraction of laboratory-generated biomass burning particles from hardwood pyrolysis. Effects of direct UVB photolysis and OH oxidation in the aqueous phase on molecular-weight-separated BrC were studied. Results indicated that the majority of low-molecular-weight (MW) BrC ( < 400 Da) was rapidly photobleached by both direct photolysis and OH oxidation on an atmospheric timescale of approximately 1 h. High MW BrC ( >= 400 Da) underwent initial photoenhancement up to similar to 15 h, followed by slow photobleaching over similar to 10 h. The laboratory experiments were supported by observations from ambient BrC samples that were collected during the fire seasons in Greece. These samples, containing freshly emitted to aged biomass burning aerosol, were analyzed for both water- and methanol-soluble BrC. Consistent with the laboratory experiments, high-MW BrC dominated the total light absorption at 365 nm for both methanol and water-soluble fractions of ambient samples with atmospheric transport times of 1 to 68 h. These ambient observations indicate that overall, biomass burning BrC across all molecular weights has an atmospheric lifetime of 15 to 28 h, consistent with estimates from previous field studies - although the BrC associated with the high-MW fraction remains relatively stable and is responsible for light absorption properties of BrC throughout most of its atmospheric lifetime. For ambient samples of aged (> 10 h) biomass burning emissions, poor linear correlations were found between light absorptivity and levoglucosan, consistent with other studies suggesting a short atmospheric lifetime for levoglucosan. However, a much stronger correlation between light absorptivity and total hydrous sugars was observed, suggesting that they may serve as more robust tracers for aged biomass burning emissions. Overall, the results from this study suggest that robust model estimates of BrC radiative impacts require consideration of the atmospheric aging of BrC and the stability of high-MW BrC. |
领域 | 地球科学 |
收录类别 | SCI-E |
WOS记录号 | WOS:000470323500002 |
WOS关键词 | HUMIC-LIKE SUBSTANCES ; SECONDARY ORGANIC AEROSOL ; LIGHT-ABSORPTION ; BLACK CARBON ; OBSERVATIONAL CONSTRAINTS ; HYDROXYL RADICALS ; OH OXIDATION ; LEVOGLUCOSAN ; CHEMISTRY ; KINETICS |
WOS类目 | Environmental Sciences ; Meteorology & Atmospheric Sciences |
WOS研究方向 | Environmental Sciences & Ecology ; Meteorology & Atmospheric Sciences |
引用统计 | |
文献类型 | 期刊论文 |
条目标识符 | http://119.78.100.173/C666/handle/2XK7JSWQ/183997 |
专题 | 地球科学 |
作者单位 | 1.Georgia Inst Technol, Sch Earth & Atmospher Sci, Atlanta, GA 30331 USA; 2.Univ Crete, Dept Chem, Environm Chem Proc Lab, Iraklion 71003, Greece; 3.Fdn Res & Technol Hellas, ICE HT, Patras 26504, Greece; 4.Natl Observ Athens, IERSD, Palea Penteli 15236, Greece; 5.Aix Marseille Univ, CNRS, IRD, Univ Toulon,MIO,UMR 7294, Toulon, France; 6.Cyprus Inst, Energy Environm & Water Res Ctr, CY-1645 Nicosia, Cyprus; 7.Ecole Polytech Fed Lausanne, Sch Architecture Civil & Environm Engn, Lab Atmospher Proc & Their Impacts, CH-1015 Lausanne, Switzerland |
推荐引用方式 GB/T 7714 | Wong, Jenny P. S.,Tsagkaraki, Maria,Tsiodra, Irini,et al. Atmospheric evolution of molecular-weight-separated brown carbon from biomass burning[J]. ATMOSPHERIC CHEMISTRY AND PHYSICS,2019,19(11):7319-7334. |
APA | Wong, Jenny P. S..,Tsagkaraki, Maria.,Tsiodra, Irini.,Mihalopoulos, Nikolaos.,Violaki, Kalliopi.,...&Weber, Rodney J..(2019).Atmospheric evolution of molecular-weight-separated brown carbon from biomass burning.ATMOSPHERIC CHEMISTRY AND PHYSICS,19(11),7319-7334. |
MLA | Wong, Jenny P. S.,et al."Atmospheric evolution of molecular-weight-separated brown carbon from biomass burning".ATMOSPHERIC CHEMISTRY AND PHYSICS 19.11(2019):7319-7334. |
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