Brown carbon (BrC) is a light-absorbing aerosol component that has a significant impact on atmospheric photochemistry and climate effects. Many studies on light absorbing characteristics of BrC (such as a fraction of water-soluble and/or water-insoluble) have been carried out in cities over the Guanzhong Basin, including radiative forcing, optical properties and sources. However, research on the Qinling Mountains is still lacking. Therefore, PM2.5 samples were collected at the northern piedmont of Qinling Mountains (QL) and Xi'an (XN) in the winter of 2020, and the optical properties and radiation effects of water extracts were analyzed and eval-uated. The mass absorption efficiency (MAE) of water-soluble organic carbon (WSOC) at 365 nm (MAE365) obtained in QL and XN were 0.18 +/- 0.03 m2 g-1 and 0.78 +/- 0.96 m2 g-1, respectively. In the ultraviolet range, the relative light absorption of WSOC relative to elemental carbon (EC) was 6.76% and 33.41% in QL and XN, respectively, and the simple forcing efficiency (SFE280-400) were 0.71 +/- 0.43 and 2.82 +/- 1.71 W g-1 in QL and XN. It may have important effects on the radiation balance of regional climate systems. The chromophores in WSOC of XN and QL are mainly composed of humic-like and protein-like substances, and humus-like substances play a dominant role in two sites (52.61% and 71.13%). Biomass combustion has a limited contribution to chromophore abundance in WSOC of QL, which is more affected by urban transmission. The fluorescence index revealed that the chromophores in WSOC had autogenous characteristics and that the organic matter was mostly newly generated. Furthermore, the molecular weight and aromatic degree in XN samples were higher than that in QL, indicating a greater capacity for light absorption. This work will be instrumental in assessing the inter-action and influence between the city and the northern piedmont of the Qinling Mountains and improve the capability of air pollution prevention and control of Guanzhong Basin.

One year of online total gaseous mercury (TGM) measurements were carried out for the first time in Lanzhou, a city in northwest China that was once seriously polluted. Measurements were made from October 2016 to October 2017 using the Tekran 2537B instrument, and the annual mean concentration of TGM in Lanzhou was 4.48 +/- 2.32 ng m(-3) (mean +/- standard deviation). TGM concentrations decreased during the measurement period, with autumn 2017 average concentrations 2.87 ng m(-3) lower than autumn 2016 average concentrations. Similar diurnal variations of TGM were obtained in different seasons with low concentrations observed in the afternoon and high concentrations at night. The principal component analysis and conditional probability function results revealed that the sources of mercury were similar to the other atmospheric pollutants such as SO2, CO, NO2 and PM2.5, and were mainly from industrial combustion plants in urban districts. Concentration weighted trajectory analysis using backward trajectories demonstrated that higher mercury concentrations were related to air masses from adjacent regions, indicating the importance of influences from local-to-regional scale sources. A synthesis of multi-decadal atmospheric mercury measurements in Lanzhou and other Chinese megacities revealed that atmospheric mercury concentrations were either generally stable or experienced a slight decrease, during a time when China implemented control measures on atmospheric pollution. Long-term atmospheric mercury observations in urban and background sites in China are warranted to assess mercury pollution and the effectiveness of China's mercury control policies. (C) 2020 Elsevier B.V. All rights reserved.