Biomass burning play a key role in the global carbon cycle by altering the atmospheric composition, and affect regional and global climate. Despite its importance, a very few high-resolution records are available worldwide, especially for recent climate change. This study analyzes levoglucosan, a specific tracer of biomass burning emissions, in a 38-year ice core retrieved from the Shulehe Glacier No. 4, northeastern Tibetan Plateau. The levoglucosan concentration in the Shulehe Glacier No. 4 ice core ranged from 0.1 to 55 ng mL(-1), with an average concentration of 8 +/- 8 ng mL(-1). The concentrations showed a decreasing trend from 2002 to 2018. Meanwhile, regional wildfire activities in Central Asian also exhibited a declining trend during the same period, suggesting the potential correspondence between levoglucosan concentration of the Shulehe Glacier No. 4 ice core and the fire activity of Central Asia. Furthermore, a positive correlation also exists between the levoglucosan concentration of the Shulehe Glacier No. 4 ice core and the wildfire counts in Central Asia from 2002 to 2018. While backward air mass trajectory analysis and fire spots data showed a higher distribution of fire counts in South Asia compared to Central Asia, but the dominance of westerly circulation in the northern TP throughout the year. Therefore, the levoglucosan in the Shulehe Glacier No. 4 provides clear evidence of Central Asian wildfire influence on Tibetan Plateau glaciers through westerlies. This highlights a great importance of ice core data for wildfire history reconstruction in the Tibetan Plateau Glacier regions.

To elucidate the molecular composition and sources of organic aerosols in Central Asia, carbonaceous compounds, major ions, and 15 organic molecular tracers of total suspended particulates (TSP) were analyzed from September 2018 to August 2019 in Dushanbe, Tajikistan. Extremely high TSP concentrations (annual mean +/- std: 211 +/- 131 mu gm(-3)) were observed, particularly during summer (seasonal mean +/- std: 333 +/- 183 mu g m(- 3)). Organic carbon (OC: 11.9 +/- 7.0 mu gm(-3)) and elemental carbon (EC: 5.1 +/- 2.2 mu gm(-3)) exhibited distinct seasonal variations from TSP, with the highest values occurring in winter. A high concentration of Ca2+ was observed (11.9 +/- 9.2 mu g m(-3)), accounting for 50.8% of the total ions and reflecting the considerable influence of dust on aerosols. Among the measured organic molecular tracers, levoglucosan was the predominant compound (632 +/- 770 ng m(-3)), and its concentration correlated significantly with OC and EC during the study period. These findings highlight biomass burning (BB) as an important contributor to the particulate air pollution in Dushanbe. High ratios of levoglucosan to mannosan, and syringic acid to vanillic acid suggest that mixed hardwood and herbaceous plants were the main burning materials in the area, with softwood being a minor one. According to the diagnostic tracer ratio, OC derived from BB constituted a large fraction of the primary OC (POC) in ambient aerosols, accounting for an annual mean of nearly 30% and reaching 63% in winter. The annual contribution of fungal spores to POC was 10%, with a maximum of 16% in spring. Measurements of plant debris, accounting for 3% of POC, divulged that these have the same variation as fungal spores.

Biomass burning (BB) has a significant influence on the Arctic environment. Here, we determined the atmospheric levels of BB-specific tracer compounds such as levoglucosan (Lev), galactosan (Gan), and mannosan (Man) in Arctic aerosols during 2010-2018. The average concentrations of Lev during the study period ranged between 0.43 and 4.15 ng m(-3). Both Lev/Man (0-30) and Man/Gan (0-3) ratios further suggested their origin from softwood/hardwood burning. The North Atlantic Oscillation (NAO) was the main driver of the Lev variability during the study period and Lev could be advected to Arctic air during the NAO was in a positive phase. Based upon the levels of Lev, black carbon (BC) generated from BB was estimated, and the corresponding radiative forcing was then calculated by Santa Barbara DISORT Atmospheric Radiative Transfer. BC has a potential warming effect in the atmosphere (+4.28 W/m(2)) while shows a cooling effect on the surface, which is equivalent to a large volcanic eruption (-3 W/m(2)). Since climate change is expected to intensify BB around the Arctic, such BC aerosols should be considered in future climate model projections.

Tibetan glaciers are natural documents of the specific biomass burning biomarker levoglucosan from regions around. However, knowledge about the characteristics of levoglucosan distributions on Tibetan glaciers under the different climate systems is poorly understood. In this study, we detected levoglucosan in snow samples from the Zuoqiupu (ZQP) Glacier affected by the Indian summer monsoon and the Muji (MJ) Glacier dominated by the westerlies. Results found that the ZQP Glacier was more heavily affected by fire emissions than the MJ Glacier, caused by stronger emission sources on the windward direction and shorter transport distances. Elevations for the appearance of levoglucosan maxima on glacier surfaces are roughly around the equilibrium line altitudes. However, levoglucosan displays a wider distribution range on the MJ glacier than on the ZQP glacier due to weaker summer melt. Injection height of fire smokes and glacial melt can affect the altitudinal distribution of levoglucosan. Black carbon and levoglucosan show different temporal variations in snow-pit samples on those two glaciers. The post depositional effects, e.g. the melting and refreezing processes, can modulate the vertical distribution of levoglucosan in snow/ice layers. Our results are helpful for understanding the geochemical behaviors of levoglucosan happened on Tibetan glacier surfaces. (C) 2016 Elsevier Ltd. All rights reserved.