Department of Earth Sciences, Indian Institute of Science Education and Research (IISER) Kolkata, Mohanpur, 741246, Nadia, India.
Department of Chemical Sciences, Indian Institute of Science Education and Research (IISER) Kolkata, Mohanpur, 741246, Nadia, India.
Sci Total Environ. 2020 May 10;716:137102. doi: 10.1016/j.scitotenv.2020.137102. Epub 2020 Feb 4.
We report here measurements of aerosol black carbon (BC) and aqueous and methanol-extractable brown carbon (BrC and BrC) from a receptor location in the eastern Indo-Gangetic Plain (IGP) under two aerosol regimes: the photochemistry-dominated summer and biomass burning (BB) dominated post-monsoon. We couple time-resolved measurements of BC and aerosol light absorption coefficients (b) with time-integrated analysis of BrC UV-Vis and fluorescence characteristics, along with measurements of total and water-soluble organic carbon (OC and WSOC), and ionic species (NH, K, NO). In the BB regime, BC and its BB-derived fraction (BC) increased by factors of 3-4 over summertime values. In comparison, b and b (absorption coefficients of BrC and BrC at 365 nm) increased by a factor of 5 (9.7 ± 7.8 vs 2.1 ± 1.4 Mm) and 2.5 (17.2 ± 9.0 vs 6.9 ± 2.9 Mm), respectively, in the BB period over summer, and were highly correlated (r = 0.82-0.87; p < 0.01) with the BB-tracer nssK. The wavelength dependence of b (Ångstrom exponent: 5.9-6.2) and the presence of characteristic fluorescence peaks at 420-430 nm suggested presence of humic-like substances (HULIS) in the aged BB aerosol, while significant association between BrC and NO (r = 0.73; p < 0.01) possibly indicated formation of water-soluble nitroaromatic compounds. BrC contributed 55% to total BrC absorption at 300-400 nm while that for the water-insoluble component (WI-BrC) increased from 41% at 340 nm to ~60% at 550 nm, suggesting formation of water-insoluble polycyclic aromatic hydrocarbons (PAHs) and/or N-PAHs. Mass absorption efficiencies at 365 nm (MAE) of BrC and BrC in the BB regime (0.95 ± 0.45 and 1.17 ± 0.78 m g, respectively) were in line with values expected from photobleaching of BB source emissions after transport to the eastern IGP. Overall, BrC and BrC were significant components of light absorbing aerosol in the BB regime, with contributions of 9 ± 5% and 16 ± 7%, respectively, to radiative forcing vis-à-vis BC in the 300-400 nm range.
我们在此报告了在两种气溶胶状态下,即光化学反应主导的夏季和生物质燃烧(BB)主导的后季风期间,在印度恒河平原东部(IGP)的一个受体位置测量的气溶胶黑碳(BC)和水相及甲醇提取物棕碳(BrC 和 BrC)。我们将 BC 和气溶胶光吸收系数(b)的时间分辨测量与 BrC UV-Vis 和荧光特性的时间积分分析相结合,同时测量总有机碳(OC 和 WSOC)和离子物种(NH、K、NO)。在 BB 期间,BC 和其源自 BB 的部分(BC)的浓度比夏季时增加了 3-4 倍。相比之下,b 和 b(365nm 处 BrC 和 BrC 的吸收系数)在 BB 期间分别增加了 5 倍(9.7±7.8 与 2.1±1.4mm)和 2.5 倍(17.2±9.0 与 6.9±2.9mm),且与 BB 示踪剂 nssK 高度相关(r=0.82-0.87;p<0.01)。b 的波长依赖性(Angstrom 指数:5.9-6.2)和 420-430nm 处特征荧光峰的存在表明,老化的 BB 气溶胶中存在腐殖质样物质(HULIS),而 BrC 与 NO 之间存在显著相关性(r=0.73;p<0.01),这可能表明形成了水溶性硝基芳烃化合物。BrC 对 300-400nm 处总 BrC 吸收的贡献为 55%,而水不溶性部分(WI-BrC)的贡献从 340nm 处的 41%增加到 550nm 处的~60%,这表明形成了水不溶性多环芳烃(PAHs)和/或 N-PAHs。在 BB 期间,BrC 和 BrC 在 365nm 处的质量吸收效率(MAE)(分别为 0.95±0.45 和 1.17±0.78m2g-1)与在向印度恒河平原东部输送后,BB 源排放光致褪色的预期值一致。总体而言,BrC 和 BrC 是 BB 期间吸光气溶胶的重要组成部分,在 300-400nm 范围内,它们对辐射强迫的贡献分别为 9±5%和 16±7%,相对于 BC。