The Modern-Era Retrospective analysis for Research and Applications, Version 2 (MERRA-2) is widely used as an advanced model dataset for the understanding of global climate change. However, independent validation and comparison of MERRA-2 are both insufficient and always desired. Therefore, in this study, the quantitative evaluation of MERRA-2 aerosol products was conducted over China for Aerosol Optical Depth (AOD), Angstrom exponent (AE), absorbing AOD (AAOD) and chemical components (black carbon (BC) and dust (DU)) using Sun sky radiometer Observation NETwork (SONET) ground-based measurements and POLDER-3/PARASOL satellite products generated by the GRASP algorithm. The available MERRA-2 monthly dataset and PARASOL/GRASP monthly and seasonal products were intercompared over China. MERRA-2 AOD (550 nm) show general good agreement with SONET and PARASOL/GRASP. For example, the correlation coefficients are usually 0.6–0.85 with SONET and 0.75–0.85 with PARASOL/GRASP, the bias is usually −0.293 to +0.008 with SONET. For AE and AAOD, the agreement is still reasonable. MERRA-2 is found to overestimate fine mode AE and to display a general underestimation of aerosol absorption over China. In addition, MERRA-2 BC and DU mass concentrations show spatial and quantitative consistency with PARASOL/GRASP components climatological products. The relatively high columnar BC mass concentration is observed around 1.5–2 mg/m³ over the East China industrial region and high DU mass concentration is around 150 mg/m³ near Taklimakan desert. MERRA-2 shows slightly higher BC and lower DU concentration than PARASOL/GRASP over East China. The evaluations with in situ BC measurements near surface verify the overestimation (MAE = +0.44 µg/m²) of MERRA-2 and underestimation (MAE = −0.38 µg/m²) of PARASOL/GRASP. The analysis demonstrates multi-source datasets, such as ground-based, space-borne remote sensing, in situ measurements, model simulation as well as reanalysis data, complement each other and can be used to refine aerosol characterization.

With the fast development of the economy and expansion, a large number of people have concentrated in Beijing over the past few decades, leading to the result that Beijing has become home to one of the most complex mixtures of aerosol types in the world. The various aerosol types play different roles in the determination of global climate change, visibility, and human health. However, to the best of our knowledge, research has rarely analyzed the correlation between aerosol types and air quality index (AQI) in Beijing (urban and suburban) over a long-term series of observations. Therefore, in this study, we aim to identify and discuss the different aerosol types and AQI in Beijing from 2004 to 2015. The aerosol types are classified into six categories: dust, mixed, highly-absorbing, moderately-absorbing, slightly-absorbing, and scattering by a multiple clustering method with the fine mode fraction (FMF) and single scattering albedo (SSA) data of retrievals from the global Aerosol Robotic Network (AERONET) sun photometer sites. The AQI levels: are good (0–50); moderate (51–100); unhealthy for sensitive groups (101–150); unhealthy (151–200); very unhealthy (201–300); and hazardous (>300). The results show that a significant FMF variability occurred among different seasons in Beijing, with maximum values present in spring and minimum values in winter. The SSA values exhibit variation, with small fluctuations from season to season. In the case of BJ station, the scattering aerosols are more frequent in summer (39%) and less in winter (1%), while the coarse particles (dust) are more frequent in spring (18%) and less in autumn (6%). In contrast, the absorbing aerosols (especially slightly-absorbing) are more frequent in summer (35%) and winter (15%). However, the mixed aerosol types are more frequent in spring (38%) and less in summer (8%). There is a similar seasonal variation in XH. In the past 12 years, the slightly-absorbing aerosol type in Beijing has increased by approximately 14%, which is believed to be due to the rapid development of industrial cities. In addition, comparing the urban and suburban regions, the slightly-absorbing aerosol type is the dominant aerosol type in both areas. Furthermore, to identify the dominant aerosol types which lead to air pollution, a related analysis was carried out by analyzing different aerosol types and the relationship between aerosol types and AQI. The results indicate that the air pollution was strongly correlated to slightly-absorbing aerosols, in which the percentage of slightly-absorbing aerosols was about 49% during the hazardous days in 2013–2015, and the correlation between AQI and aerosol types is also strong (R² = 0.76 and 0.97, in Beijing and Xianghe).

Miyun Reservoir is the major water source for Bijing, China. Currently, the water quality of Miyun reservoir is meso - trophict, mainly dur to the non-point source pollution (NPS) in the watershed. Phosphorus (P) is the limited factor. In this paper, Chaohe River basin, upstream of the Miyun Reservoir, is chosen as the study area, A modified P Index was developed to identify critical source areas (CSAs) of non-point source pollution by analyzing local hydrological and meteorological data, land use, soil, soil conservation, farmland management, population density, and livestock. The factors of livestock and population density are new factors added to the P Index system based on the actual local characteristics. It was found that the loss P from high-risk area accounts for only 7.95%. These areas are located mainly along streams. Livestock factor and the population density factor are most closely related to the CSAs downstream of Chaohe River basin. The management strategies are outlined according to the distribution characteristics of the critical source areas.

Pollution haze is a frequent phenomenon in the North China Plain (NCP) appearing during winter when the aerosol is affected by various pollutant sources and has complex distribution of the aerosol properties, while different aerosol components may have various critical effects on air quality, human health and radiative balance. Therefore, large-scale and accurate aerosol components characterization is urgently and highly desirable but hardly achievable at the regional scale. In this respect, directional and polarimetric remote sensing observations have great potential for providing information about the aerosol components. In this study, a state-of-the-art GRASP/Component approach was employed for attempting to characterize aerosol components in the NCP using POLDER/PARASOL satellite observations. The analysis was done for January 2012 in Beijing (BJ) and Shanxi (SX). The results indicate a peak of the BC mass concentration in an atmospheric column of 82.8 mg/m² in the SX region, with a mean of 29.2 mg/m² that is about four times higher than one in BJ (8.9 mg/m²). The mean BrC mass concentrations are, however, higher in BJ (up to ca. 271 mg/m²) than that in SX, which can be attributed to a higher anthropogenic emission. The mean amount of fine ammonium sulfate-like particles observed in the BJ region was three times lower than in SX (131 mg/m²). The study also analyzes meteorological and air quality data for characterizing the pollution event in BJ. During the haze episode, the results suggest a rapid increase in the fine mode aerosol volume concentration associated with a decrease of a scale height of aerosol down to 1500 m. As expected, the values of aerosol optical depth (AOD), absorbing aerosol optical depth (AAOD) and fine mode aerosol optical depth (AOD_f) are much higher on hazy days. The mass fraction of ammonium sulfate-like aerosol increases from about 13% to 29% and mass concentration increases from 300 mg/m² to 500 mg/m². The daily mean PM_2.5 concentration and RH independently measured during these reported pollution episodes reach up to 425 g/m³ and 80% correspondingly. The monthly mean mass concentrations of other aerosol components in the BJ are found to be in agreement with the results of previous research works. Finally, a preliminary comparison of these remote sensing derived results with literature and in situ PM_2.5 measurements is also presented.