Atmospheric brown carbon (BrC), a short-lived climate forcer, absorbs solar radiation and is a substantial contributor to the warming of the Earth ' s atmosphere. BrC composition, its absorption properties, and their evolution are poorly represented in climate models, especially during atmospheric aqueous events such as fog and clouds. These aqueous events, especially fog, are quite prevalent during wintertime in Indo-Gangetic Plain (IGP) and involve several stages (e.g., activation, formation, and dissipation, etc.), resulting in a large variation of relative humidity (RH) in the atmosphere. The huge RH variability allowed us to examine the evolution of water-soluble brown carbon (WS-BrC) diurnally and as a function of aerosol liquid water content (ALWC) and RH in this study. We explored links between the evolution of WS-BrC mass absorption efficiency at 365 nm (MAE WS- BrC-365 ) and chemical characteristics, viz., low-volatility organics and water-soluble organic nitrogen (WSON) to water-soluble organic carbon (WSOC) ratio (org-N/C), in the field (at Kanpur in central IGP) for the first time worldwide. We observed that WSON formation governed enhancement in MAE WS-BrC-365 diurnally (except during the afternoon) in the IGP. During the afternoon, the WS-BrC photochemical bleaching dwarfed the absorption enhancement caused by WSON formation. Further, both MAE WS-BrC-365 and org-N/C ratio increased with a decrease in ALWC and RH in this study, signifying that evaporation of fog droplets or bulk aerosol particles accelerated the formation of nitrogen-containing organic chromophores, resulting in the enhancement of WS-BrC absorptivity. The direct radiative forcing of WS-BrC relative to that of elemental carbon (EC) was -19 % during wintertime in Kanpur, and - 40 % of this contribution was in the UV -region. These findings highlight the importance of further examining the links between the evolution of BrC absorption behavior and chemical composition in the field and incorporating it in the BrC framework of climate models to constrain the predictions.

Atmospheric nitrogen is ubiquitous in the environment and hence plays an essential role in the nutrient balance over the whole ecosystem. However, its abundance and characteristics, particularly in the Himalayas, are not well understood. Therefore, to understand the abundance, sources, and seasonality of soluble nitrogenous species in the middle hills of the central Himalayas, aerosol samples were collected at Dhulikhel in Nepal from January to December 2018. The results of this study revealed that water-soluble inorganic nitrogen (WSIN) contributed the most to water-soluble total nitrogen with an abundance of ammonium nitrogen (NH4+-N). Moreover, watersoluble organic nitrogen (WSON) contributed approximately 18% to aerosol total water-soluble nitrogen. The aerosol mass and WSIN species exhibited strong seasonality with considerably higher concentrations during dry periods and lower concentrations during the wet period. Furthermore, for dry periods, the HYSPLIT model revealed that nitrogen aerosols mainly originated from the Indo-Gangetic Plain region and were transported and deposited in the Himalayas through long-range atmospheric transport. The strong correlations of WSON with nss-K+ (biomass burning) and nss-Ca2+ (crustal sources) and lack of a significant correlation with SO42- indicated that primary sources are responsible for generating WSON rather than secondary processes in the Himalayas. The estimated dry deposition fluxes for NO3--N, NH4+-N, and WSON were 1.56, 8.35, and 4.06 kg ha(-1) y(-1), respectively. This study also shows that increasing air contaminants and emissions over South Asia can enter the Himalayas and affect the human health and ecology of this fragile area.