Biomass burning (BB) is a significant air pollution source, with global, regional and local impacts on air quality, public health and climate. Worldwide an extensive range of studies has been conducted on almost all the aspects of BB, including its specific types, on quantification of emissions and on assessing its various impacts. China is one of the countries where the significance of BB has been recognized, and a lot of research efforts devoted to investigate it, however, so far no systematic reviews were conducted to synthesize the information which has been emerging. Therefore the aim of this work was to comprehensively review most of the studies published on this topic in China, including literature concerning field measurements, laboratory studies and the impacts of BB indoors and outdoors in China. In addition, this review provides insights into the role of wildfire and anthropogenic BB on air quality and health globally. Further, we attempted to provide a basis for formulation of policies and regulations by policy makers in China.

[1] Collocated measurements of the mass concentrations of aerosol black carbon (BC) and composite aerosols near the surface were carried out along with spectral aerosol optical depths (AODs) from a high-altitude station, Manora Peak in central Himalayas, during a comprehensive aerosol field campaign in December 2004. Despite being a pristine location in the Shivalik Ranges of central Himalayas and having a monthly mean AOD (at 500 nm) of 0.059 ± 0.033 (typical to this site), total suspended particulate (TSP) concentration was in the range 15-40 mg m À3 (mean value 27.1 ± 8.3 mg m À3 ). Interestingly, aerosol BC had a mean concentration of 1.36 ± 0.99 mg m À3 and contributed $5.0 ± 1.3% to the composite aerosol mass. This large abundance of BC is found to have linkages to the human activities in the adjoining valley and to the boundary layer dynamics. Consequently, the inferred single scattering albedo lies in the range of 0.87 to 0.94 (mean value 0.90 ± 0.03), indicating significant aerosol absorption. The estimated aerosol radiative forcing was as low as À4.2 W m À2 at the surface, +0.7 W m À2 at the top of the atmosphere, implying an atmospheric forcing of +4.9 W m À2 . Though absolute value of the atmospheric forcing is quite small, which arises primarily from the very low AOD (or the column abundance of aerosols), the forcing efficiency (forcing per unit optical depth) was $88 W m À2 , which is attributed to the high BC mass fraction.

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