No abstract

No abstract

No abstract

The Tibetan Plateau (TP) has received wide scientific concern in recent decades owing to its important impacts on regional climatic and cryospheric changes, hydrological cycles, and environments. However, our understanding of the spatial distribution of the chemical and optical properties of aerosols is still limited based on prior single‐site observations. In this study, aerosol light absorptions from black carbon (BC) and brown carbon (BrC) were explored and compared among three remote TP sites, including Qomolangma Station (QOMS) on the southern TP, Nam Co Station (NamCo) on the central TP, and Waliguan Observatory on the northeastern TP. Although the aerosol mass concentration at QOMS was less than half of that at Waliguan, the light absorption coefficient of aerosols at QOMS was nearly 5 times higher than that at Waliguan, mainly as a result of more light‐absorbing carbonaceous aerosols on the southern TP due to long‐range transported biomass burning emissions. Specifically, BC dominated aerosol light absorption at all wavelengths, whereas BrC contributed ∼30% of the light absorption at 370 nm at QOMS and ∼20% at Waliguan and NamCo. A major contributor to BrC light absorption at QOMS was biomass burning‐related organic aerosols apportioned from aerosol mass spectrometry measurements. Understanding the significant regional differences in aerosol light absorption properties on the TP is useful for evaluating the regional climatic and environmental effects and validating the model results on aerosol radiative forcing.