Abstract

Abstract. Light-absorbing aerosol – particularly elemental carbon (EC) – while mixed with snow and ice is an important climate driver from the enhanced absorption of solar radiation. Currently, considerable efforts are being made to estimate its radiative forcing on a global scale, but several uncertainties remain, particularly those regarding its deposition processes. In this study, concurrent measurements of EC in air and snow are performed for three years (2009–2012) at Changbai station, northeastern China. The scavenging ratio and the wet- and dry-deposition fluxes of EC over the snow surface are estimated. The mean EC concentration in the surface snow is 1000 ± 1500 ng g−1, ranging from 7 to 7640 ng g−1. The mean value of the scavenging ratio of EC by snow is 140 ± 100, with a median value of 150, which is smaller than that reported in Arctic areas. A non-rimed snow process is a significant factor in interpreting differences with Arctic areas. Wet-deposition fluxes of EC are estimated to be 0.47 ± 0.37 μg cm−2 month−1 on average over the three snow seasons studied. Dry deposition is more than five times higher, with an average of 2.65 ± 1.93 μg cm−2 month−1; however, only winter period estimation is possible (December–February). During winter in Changbai, 87% of EC in snow is estimated to be due to dry deposition, with a mean dry deposition velocity of 6.44 × 10−3 m s−1 and median of 8.14 × 10−3 m s−1. Finally, the calculation of the radiative effect shows that 500 ng g−1 of dry-deposited EC to a snow surface absorbs three times more incoming solar energy than the same mass mixed in the snow through wet deposition. Deposition processes of an EC-containing snow surface are, therefore, crucial to estimate its radiative forcing better, particularly in northeastern China, where local emission strongly influences the level and gradient of EC in the snowpack, and snow-covered areas are cold and dry due to the atmospheric general circulation. Furthermore, this study builds on the knowledge to characterize the conditions in the snow-laden Chinese rural areas better as well as to constrain transport of EC to the Arctic better.

Highlights

  • Elemental carbon (EC) is emitted from incomplete combustion of coal, fossil fuel, and biomass burning (Novakov et al, 2003; Jacobson, 2004)

  • The EC concentration ranges from 7 to 7640 ng g−1, with a mean value of 1000 ± 1500 ng g−1. These concentrations are considerably higher than the values measured in the Himalayas and in western China, which were typically lower than 100 ng g−1 (Ming et al, 2008; Xu et al, 2009), and two orders of magnitude higher than those reported by Forsström et al (2009) and Doherty et al (2010) for Arctic areas

  • A comparison with other snow seasons shows that a higher load of black carbon (BC) in the snow surface appeared in the snow season of 2011–2012, with moderate BC concentration in air and precipitation in a slightly colder winter

Read more

Summary

Introduction

Elemental carbon (EC) is emitted from incomplete combustion of coal, fossil fuel, and biomass burning (Novakov et al, 2003; Jacobson, 2004). EC warms up the atmosphere by absorbing solar radiation while being suspended as in air, as well as by reducing the surface albedo while mixed with snow and ice. EC warms up the atmosphere by absorbing solar radiation while being suspended as in air, as well as by reducing the surface albedo while mixed with snow and ice Both in air and on snow or ice, EC exerts a net positive forcing on the climate. EC particles may influence cloud properties by acting as a nucleus for hydrometeors. This so-called indirect climate effect, via influencing cloud microphysical properties, is poorly understood. Several studies have highlighted that EC (through positive feedback mechanisms) is the second most important climate warming driver after CO2 and could be in some regions comparable to greenhouse gas forcing (Bachmann, 2009; Shindell and Faluvegi, 2009)

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call