[Analysis of Seasonal Variations in Chemical Characteristics and Sources of PM2.5 During Summer and Winter in Ji'nan City].

To investigate seasonal variations in the chemical compositions of aerosols in Ji'nan City, PM2.5 samples were collected during summer and winter in 2015. The sampling period lasted one month during each season. PM2.5 samples were analyzed for the composition, concentration, and sources of water-soluble inorganic ions, organic carbon (OC), elemental carbon (EC), and water-soluble organic carbon (WSOC). Results showed that mass concentrations of PM2.5 in winter were about twice those in summer, and concentration levels varied between fine and excellent. The concentrations of total water-soluble inorganic ions were also higher in winter than in summer, with SO42-, NO3-, and NH4+ being the dominant species and well correlated with each other. NH4+ in PM2.5 mostly existed in the form of (NH4)2SO4 and NH4NO3 in both summer and winter. There was strong secondary oxidation of SO2 and NO2. The sulfate oxidizing rate (SOR) was higher in summer than in winter, while the nitrate oxidizing rate (NOR) showed the opposite trend. The ratio of anions to cations in both summer and winter were less than one, suggesting that PM2.5 were slightly alkaline. The ISORROPIA-Ⅱ mode showed that acidity in winter was stronger than in summer. Concentations of OC and EC were both higher in winter than in summer. The ratios of OC to EC and WSOC to OC and estimated concentrations of secondary organic carbon (SOC) showed that secondary pollution was more serious in winter than in summer. Principal component analysis(PCA)indicated that the major sources contributing to inorganic ions were secondary oxidation and biomass burning in summer, and coal combustion and secondary pollutants formed by chemical oxidation of precursors emitted from coal combustion in winter.

[Seasonal Variation and Sources of Dicarboxylic Acids and Related Compounds in PM10 from Mt. Huangshan].

To identify the seasonal variation of dicarboxylic acids and related compounds in PM10 from Mt. Huangshan. PM10samples were collected during the summer and winter of 2015, which were then analyzed for dicarboxylic acids, ketocarboxylic acids, and α-dicarbonyls. The results showed that oxalic acid(HOOC-COOH, C2) was the dominant species in the summer and winter months, followed by malonic acid(HOOC-CH2-COOH, C3), and succinic acid[HOOC-(CH2)2-COOH, C4], being consistent with that in other high-altitude regions. Most of the diacids were more abundant in the summer months than in the winter months, while adipic acid(C6) and phahalic acid(Ph) were twice lower in the summer months, suggesting significant impact of anthropogenic pollution on the wintertime alpine atmosphere. Moreover, as major precursors of C2, glyoxal(Gly) and methylglyoxal(mGly) were also lower in the summer months than in the winter months, which were opposite to those of the diacids, indicating that the mountain troposphere was more oxidative in the summer months than in the winter months. Principal component analysis(PCA) further revealed that the wintertime SOA in the Mt. Huangshan troposphere mostly originated from the anthropogenic pollutants from long-distance transport. Conversely, the summertime SOA mostly originated from the further oxidation of the mountainous biogenic sources. The AIM(Aerosol Inorganic Model) calculation results showed that the aqueous-phase C2 production was the primary mechanism of C2 formation in ambient aerosol and was driven by acid-catalyzed oxidation in summer.

Influence of intermittent water releases on groundwater chemistry at the lower reaches of the Tarim River, China.

Based on the data of the depths and the chemical properties of groundwater, salinity in the soil profile, and the basic information on each delivery of water collected from the years 2000 to 2006, the varied character of groundwater chemistry and related factors were studied. The results confirmed the three stages of the variations in groundwater chemistry influenced by the intermittent water deliveries. The factors that had close relations to the variations in groundwater chemistry were the distances of monitoring wells from the water channel, the depths of the groundwater, water flux in watercourse, and the salinities in soils. The relations between chemical variation and groundwater depths indicated that the water quality was the best with the groundwater varying from 5 to 6 m. In addition, the constructive species in the study area can survive well with the depth of groundwater varying from 5 to 6 m, so the rational depth of groundwater in the lower reaches of the Tarim River should be 5 m or so. The redistribution of salts in the soil profile and its relations to the chemical properties and depths of groundwater revealed the linear water delivery at present combining with surface water supply in proper sections would promote water quality optimized and speed up the pace of ecological restoration in the study area.