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Long-term variations in solar radiation, diffuse radiation, and diffuse radiation fraction caused by aerosols in China during 1961-2016.

ABSTRACT: The effects of atmospheric aerosols on the terrestrial climate system are more regional than those of greenhouse gases, which are more global. Thus, it is necessary to examine the typical regional effects of how aerosols affect solar radiation in order to develop a more comprehensive understanding. In this study, we used global AErosol RObotic NETwork (AERONET) data and robust radiation observational evidence to investigate the impact of aerosols on total radiation, diffuse radiation, and the diffuse radiation fraction in China from 1961 to 2016. Our results showed that there were different temporal changes in the aerosol optical depth (AOD), total solar radiation, diffuse radiation and diffuse radiation fraction over the past 56 years. Specifically, the 550 nm AOD from 2005 to 2016 decreased significantly, with annual average AOD of 0.51. Meanwhile, the average total solar radiation reduced by 2.48%, while there was a slight increase in average diffuse radiation at a rate of 3.10 MJ·m-2·yr-1. Moreover, the spatial heterogeneities of AOD, total radiation, diffuse radiation, and the diffuse radiation fraction in China were significant. Aerosol particle emissions in the developed eastern and southern regions of China were more severe than those in the western regions, resulting in higher total radiation and diffuse radiation in the western plateau than in the eastern plain. In addition, aerosols were found to have negative effects on total radiation and sunshine hours, and positive effects on diffuse radiation and diffuse radiation fraction. Further, the diffuse radiation fraction was negatively correlated with sunshine hours. However, there was a positive correlation between AOD and sunshine hours. These results could be used to assess the impacts of climate change on terrestrial ecosystem productivity and carbon budgets.

SUBMITTER: Xie H

PROVIDER: S-EPMC8092767 | biostudies-literature |

REPOSITORIES: biostudies-literature

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Project description:An empirical model to estimate global solar radiation was developed at Qomolangma Station using observed solar radiation and meteorological parameters. The predicted hourly global solar radiation agrees well with observations at the ground in 2008-2011. This model was used to calculate global solar radiation at the ground and its loss in the atmosphere due to absorbing and scattering substances in 2007-2020. A sensitivity analysis shows that the responses of global solar radiation to changes in water vapor and scattering factors (expressed as water-vapor pressure and the attenuation factor, AF, respectively) are nonlinear, and global solar radiation is more sensitive to changes in scattering than to changes in absorption. Further applying this empirical model, the albedos at the top of the atmosphere (TOA) and the surface in 2007-2020 were computed and are in line with satellite-based retrievals. During 2007-2020, the mean estimated annual global solar radiation increased by 0.22% per year, which was associated with a decrease in AF of 1.46% and an increase in water-vapor pressure of 0.37% per year. The annual mean air temperature increased by about 0.16 °C over the 14 years. Annual mean losses of solar radiation caused by absorbing and scattering substances and total loss were 2.55, 0.64, and 3.19 MJ m-2, respectively. The annual average absorbing loss was much larger than the scattering loss; their contributions to the total loss were 77.23% and 22.77%, indicating that absorbing substances play significant roles. The annual absorbing loss increased by 0.42% per year, and scattering and total losses decreased by 2.00% and 0.14% per year, respectively. The estimated and satellite-derived annual albedos increased at the TOA and decreased at the surface. This study shows that solar radiation and its interactions with atmospheric absorbing and scattering substances have played key but different roles in regional climate and climate change at the three poles.

Project description:The molecular characteristics and formation mechanism of biogenic secondary organic aerosols (BSOAs) in the forested atmosphere are poorly known. Here, we report the temporal variations in and formation processes of BSOA tracers derived from isoprene, monoterpenes, and β caryophyllene in PM2.5 samples collected at the foot of Mt. Huang (483 m a. s. l) in East China during the summer of 2019 with a 3 h time resolution. The concentrations of nearly all of the detected species, including organic carbon (OC), elemental carbon (EC), levoglucosan, and SIA (sum of SO42-, NO3-, and NH4+), were higher at night (19:00-7:00 of the next day) than in the daytime (7:00-19:00). In addition, air pollutants that accumulated by the dynamic transport of the mountain breeze at night were also a crucial reason for the higher BSOA tracers. Most of the BSOA tracers exhibited higher concentrations at night than in the daytime and peaked at 1:00 to 4:00 or 4:00 to 7:00. Those BSOA tracers presented strong correlations with O3 in the daytime rather than at night, indicating that BSOAs in the daytime were primarily derived from the photo-oxidation of BVOCs with O3. The close correlations of BSOA tracers with SO42- and particle acidity (pHis) suggest that BSOAs were primarily derived from the acid-catalyzed aqueous-phase oxidation. Considering the higher relative humidity and LWC concentration at night, the promoted aqueous oxidation was the essential reason for the higher concentrations of BSOA tracers at night. Moreover, levoglucosan exhibited a robust correlation with BSOA tracers, especially β-caryophyllinic acid, suggesting that biomass burning from long-distance transport exerted a significant impact on BSOA formation. Based on a tracer-based method, the estimated concentrations of secondary organic carbon (SOC) derived from isoprene, monoterpenes, and β caryophyllene at night (0.90 ± 0.57 µgC m-3) were higher than those (0.53 ± 0.34 µgC m-3) in the daytime, accounting for 14.5 ± 8.5% and 12.2 ± 5.0% of OC, respectively. Our results reveal that the BSOA formation at the foot of Mt. Huang was promoted by the mountain-valley breezes and anthropogenic pollutants from long-range transport.

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Long-term variations in solar radiation, diffuse radiation, and diffuse radiation fraction caused by aerosols in China during 1961-2016.

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