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Title: Re-evaluating black carbon in the Himalayas and the Tibetan Plateau: Concentrations and deposition
Authors: Li, C
Yan, F
Kang, S
Chen, P
Han, X
Hu, Z
Zhang, G
Hong, Y
Gao, S
Qu, B 
Zhu, Z
Li, J
Chen, B
Sillanpaä, M
Keywords: arid environment
atmospheric chemistry
atmospheric deposition
black carbon
carbon dioxide
concentration (composition)
Qinghai-Xizang Plateau
Issue Date: 2017
Publisher: Copernicus Publications
Citation: Li, C, Yan, F, Kang, S, Chen, P, Han, X, Hu, Z, Zhang, G, Hong, Y, Gao, S, Qu, B, Zhu, Z, Li, J, Chen, B, Sillanpaä, M (2017). Re-evaluating black carbon in the Himalayas and the Tibetan Plateau: Concentrations and deposition. Atmospheric Chemistry and Physics 17 (19) : 11899-11912. ScholarBank@NUS Repository.
Rights: Attribution 4.0 International
Abstract: Black carbon (BC) is the second most important warming component in the atmosphere after CO2. The BC in the Himalayas and the Tibetan Plateau (HTP) has influenced the Indian monsoon and accelerated the retreat of glaciers, resulting in serious consequences for billions of Asian residents. Although a number of related studies have been conducted in this region, the BC concentrations and deposition rates remain poorly constrained. Because of the presence of arid environments and the potential influence of carbonates in mineral dust (MD), the reported BC concentrations in the HTP are overestimated. In addition, large discrepancies have been reported among the BC deposition derived from lake cores, ice cores, snow pits and models. Therefore, the actual BC concentration and deposition values in this sensitive region must be determined. A comparison between the BC concentrations in acid (HCl)-treated and untreated total suspected particle samples from the HTP showed that the BC concentrations previously reported for the Nam Co station (central part of the HTP) and the Everest station (northern slope of the central Himalayas) were overestimated by approximately 52±35 and 39±24 %, respectively, because of the influence of carbonates in MD. Additionally, the organic carbon (OC) levels were overestimated by approximately 22±10 and 22±12% for the same reason. Based on previously reported values from the study region, we propose that the actual BC concentrations at the Nam Co and Everest stations are 61 and 154 ngm-3, respectively. Furthermore, a comprehensive comparison of the BC deposition rates obtained via different methods indicated that the deposition of BC in HTP lake cores was mainly related to river sediment transport from the lake basin as a result of climate change (e.g., increases in temperature and precipitation) and that relatively little BC deposition occurred via atmospheric deposition. Therefore, previously reported BC deposition rates from lake cores overestimated the atmospheric deposition of BC in the HTP. Correspondingly, BC deposition derived from snow pits and ice cores agreed well with that derived from models, implying that the BC depositions of these two methods reflect the actual values in the HTP. Therefore, based on reported values from snow pits and ice cores, we propose that the BC deposition in the HTP is 17:9±5:3 mgm-2 a-1, with higher and lower values appearing along the fringes and central areas of the HTP, respectively. These adjusted BC concentrations and deposition values in the HTP are critical for performing accurate evalua-tions of other BC factors, such as atmospheric distribution, radiative forcing and chemical transport in the HTP. © 2017 Author(s).
Source Title: Atmospheric Chemistry and Physics
ISSN: 1680-7316
DOI: 10.5194/acp-17-11899-2017
Rights: Attribution 4.0 International
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