The lack of light-absorbing aerosols vertical distributions data largely limited to revealing the formation mechanism of severe haze pollution in Chinese cities. Based on the synchronous measurements of size-resolved carbonaceous aerosols and meteorological data at near surface level and hilltop (about 620 m above the valley) in Lanzhou of northwest China, this study compared organic and elemental carbon (OC, EC) size distributions at the two altitudes and revealed the key influencing factors in a typical urban valley, China. The winter OC size distributions were typically bimodal with two comparable peaks in the accumulation and coarse modes, while those in summer were unimodal with the highest value in the size bin of 4.7-5.8 mu m. The size-resolved OC and EC at near the surface were significantly higher than those at the hilltop. The difference (concentrations and size distributions) of OC and EC between the surface and hilltop in summer was much smaller than that in winter due to stronger vertical mixing and larger summer SOC contributions at the hilltop. The winds paralleling with running urban valley were conducive to dispersing the air pollutants from near the surface to the upper air. The roles of horizontal and vertical dispersions to carbonaceous aerosols were comparable at near the surface, while horizontal dispersion was more important at the hilltop. Furthermore, the vertical dispersion was a main factor controlling size-resolved carbonaceous aerosols under highly polluted conditions in a typical urban valley. This study will provide the basis for regulation of severe haze pollution over complex terrain.

The concentrations, optical and radiative effects of carbonaceous aerosols were essential to studies of the climatic, environmental and health effects. The previous studies less combined numerical simulation with in-situ observations, especially for the aerosol vertical profiles. In this study, we off-line measured vertical profiles of submicron black carbon (BC) aerosols and on-line obtained aerosol optical properties over urban Lanzhou during 26 December 2017 to 11 January 2018. The BC optical properties and radiative effects were evaluated using Optical Properties of Aerosols and Clouds (OPAC) and Santa Barbara DISORT Atmospheric Radiative Transfer (SBDART) models. The absorption and scattering coefficients and optical depth of BC aerosols ranged from 9 to 83 M m(-1) , 3-24 M m(-1) and 0.02 to 0.2 respectively, which in average accounted for 50%, 3% and 11% of the optical properties of total aerosols during the study period. BC aerosol radiative forcing (ARF) within ATMOS (top-surface) varying from 16.6 to 108.8 W m(-2) accounted for 17.3%-97.4% of total aerosols ARF with an average of 66.6%, and the percentages increased significantly as BC concentrations increased during the period. The mean atmospheric heating rate (AHR) induced by BC aerosols was 1.94 K day(-1) ranging from 0.46 to 3.03 K day(-1) during the study period. This study contributes to understanding the impacts of light-absorbing aerosols on climate and haze pollution in an urban valley.