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Biogenic volatile organic compounds (BVOCs) are important precursors to ozone and secondary organic aerosols in the atmosphere, affecting air quality, clouds, and climate. However, the trend in BVOC emissions and driving factors for the emission changes in different geographic regions over the past 2 decades has remained unclear. Here, regional to global changes in BVOC emissions during 2001–2020 are simulated using the latest Model of Emission of Gases and Aerosols from Nature (MEGANv3.2) with the input of time-varying satellite-retrieved vegetation and reanalysis meteorology data. Comparison of model simulations with the site observations shows that the model can reasonably reproduce the magnitude of isoprene and monoterpene emission fluxes. The spatial distribution of the modeled isoprene emissions is generally comparable to the satellite retrievals. The estimated annual average global BVOC emissions are 835.4 Tg yr -1 with the emissions from isoprene, monoterpenes, sesquiterpenes, and other BVOC comprised of 347.7, 184.8, 23.3, and 279.6 Tg yr -1 , respectively. We find that the decrease in global isoprene emissions (-0.07 % per year) caused by the increase in CO 2 concentrations (-0.20 % per year) is stronger than that caused by changes in vegetation (-0.03 % per year) and meteorological factors (0.15 % per year). However, regional disparities are large. Isoprene emissions increase significantly in Europe, East Asia, and South Asia (0.37 % per year–0.66 % per year). Half of the increasing trend is contributed by increased leaf area index (LAI) (maximum over 0.02 m 2 m -2 yr -1) and tree cover. Changes in meteorological factors contribute to another half, with elevated temperature dominating in Europe and increased soil moisture dominating in East and South Asia. In contrast, in South America and Southeast Asia, shifts in vegetation type associated with the BVOC emission capacity, which partly results from the deforestation and agricultural expansion, decrease the BVOC emission and offset nearly half of the emission increase caused by changes in meteorological factors. Overall, isoprene emission increases by 0.35 % per year and 0.25 % per year in South America and Southeast Asia, respectively. In Central Africa, a decrease in temperature dominates the negative emission trend (-0.74 % per year). Global monoterpene emissions show a significantly increasing trend (0.34 % per year, 0.6 Tg yr -1) compared to that of isoprene (-0.07 % per year, -0.2 Tg yr -1) , especially in strong greening hotspots. This is mainly because the monoterpene emissions are more sensitive to changes in LAI and are not subject to the inhibition effect of CO 2. The findings highlight the important roles of vegetation cover and biomass, temperature, and soil moisture in modulating the temporal variations of global BVOC emissions in the past 2 decades. [ABSTRACT FROM AUTHOR]

Biogenic volatile organic compounds (BVOCs) are important precursors to ozone and secondary organic aerosols in the atmosphere, affecting air quality, clouds and climate. However, the trend of BVOC emissions and driving factors for the emission changes in different geographic regions over the past two decades has remained unclear. Here, regional to global changes in BVOC emissions during 2001–2020 are simulated using the latest Model of Emission of Gases and Aerosols from Nature (MEGANv3.2) with the input of time-varying satellite-retrieved vegetation and reanalysis meteorology data. Comparison of model simulations with the site observations shows that the model can reasonably reproduce the magnitude of isoprene and monoterpene emission fluxes. The spatial distribution of the modeled isoprene emissions is generally comparable to the satellite retrievals. The estimated annual average global BVOC emissions are 835.4 Tg yr-1 with the emissions from isoprene, monoterpenes, sesquiterpenes, and other BVOC comprised of 347.7, 184.8, 23.3, and 279.6 Tg yr-1, respectively. We find that the decrease in global isoprene emissions (-0.07 % yr-1) caused by increase in CO2 concentrations (-0.20 % yr-1) is stronger than that caused by changes in vegetation (-0.03 % yr-1) and meteorological factors (0.15 % yr-1). However, regional disparities are large. Isoprene emissions increase significantly in Europe, East Asia, and South Asia (0.37-0.66 % yr-1). The increasing trend is contributed by half from increased leaf area index (LAI) (maximum over 0.02 m2 m-2 yr-1) and tree cover. Changes in meteorological factors contribute to another half, with elevated temperature dominating in Europe and increased soil moisture dominating in East and South Asia. In contrast, in South America and Southeast Asia, shifts in vegetation type associated with the BVOC emission capacity, which partly results from the deforestation and agricultural expansion, decrease the BVOC emission and offset nearly half of the emission increase caused by changes in meteorological factors. Overall, isoprene emission increases by 0.35 % yr-1 and 0.25 % yr-1 in South America and Southeast Asia, respectively. In Central Africa, a decrease in temperature dominates the negative emission trend (-0.74 % yr-1). Global monoterpene emissions show a significantly increasing trend (0.34 % yr-1, 0.6 Tg yr-1) compared to that of isoprene (-0.07 % yr-1, -0.2 Tg yr-1), especially in strong greening hotspots. This is mainly because the monoterpene emissions are more sensitive to changes in LAI and are not subject to the inhibition effect of CO2. The findings highlight the important roles of vegetation cover and biomass, temperature, and soil moisture in modulating the temporal variations of global BVOC emissions in past two decades. [ABSTRACT FROM AUTHOR]

Light-absorbing particles (LAPs), mainly dust and black carbon, can significantly impact snowmelt and regional water availability over high-mountain Asia (HMA). In this study, for the first time, online aerosol–snow interactions are enabled and a fully coupled chemistry Weather Research and Forecasting (WRF-Chem) regional model is used to simulate LAP-induced radiative forcing on snow surfaces in HMA at relatively high spatial resolution (12 km , WRF-HR) compared with previous studies. Simulated macro- and microphysical properties of the snowpack and LAP-induced snow darkening are evaluated against new spatially and temporally complete datasets of snow-covered area, grain size, and impurity-induced albedo reduction over HMA. A WRF-Chem quasi-global simulation with the same configuration as WRF-HR but a coarser spatial resolution (1 ∘ , WRF-CR) is also used to illustrate the impact of spatial resolution on simulations of snow properties and aerosol distribution over HMA. Due to a more realistic representation of terrain slopes over HMA, the higher-resolution model (WRF-HR) shows significantly better performance in simulating snow area cover, duration of snow cover, snow albedo and snow grain size over HMA, as well as an evidently better atmospheric aerosol loading and mean LAP concentration in snow. However, the differences in albedo reduction from model and satellite retrievals is large during winter due to associated overestimation in simulated snow fraction. It is noteworthy that Himalayan snow cover has high magnitudes of LAP-induced snow albedo reduction (4 %–8 %) in pre-monsoon seasons (both from WRF-HR and satellite estimates), which induces a snow-mediated radiative forcing of ∼30 –50 Wm-2. As a result, the Himalayas (specifically the western Himalayas) hold the most vulnerable glaciers and mountain snowpack to the LAP-induced snow darkening effect within HMA. In summary, coarse spatial resolution and absence of snow–aerosol interactions over the Himalayan cryosphere will result in significant underestimation of aerosol effects on snow melting and regional hydroclimate. [ABSTRACT FROM AUTHOR]