Progress in direct reprogramming of dopaminergic cell replacement therapy.

Parkinson's disease (PD) is a gradual neurodegenerative disease. While drug therapy and surgical treatments have been the primary means of addressing PD, they do not offer a cure, and the risks associated with surgical treatment are high. Recent advances in cell reprogramming have given rise to new prospects for the treatment of Parkinson's disease (PD), with induced pluripotent stem cells (iPSCs), induced dopamine neurons (iDNs), and induced neural stem cells (iNSCs) being created. These cells can potentially be used in the treatment of Parkinson's disease. On the other hand, this article emphasizes the limits of iPSCs and iNSCs in the context of Parkinson's disease treatment, as well as approaches for direct reprogramming of somatic cells into iDNs. The paper will examine the benefits and drawbacks of directly converting somatic cells into iDNs.

[Variations in Ozone Concentration in Seven Regions Under Different Temperature and Humidity Conditions].

In recent years, the situation of ozone pollution in China has become increasingly severe, with PM2.5 being the main pollutant in the atmospheric environment of several cities. Meteorological conditions, particularly temperature and humidity, have a great influence on ozone formation. Therefore, understanding and quantifying the impact of the variation in temperature and humidity on ozone level can effectively provide the theoretical basis for the government to prevent and control ozone pollution. By analyzing the relationship among the daily maximum temperature (Tmax), relative humidity (RH), and the maximum 8-h running average ozone (O3-8h) measured from January 1, 2015 to July 31, 2022, a linear positive correlation between O3-8h and Tmax was observed in the seven regions with serious ozone pollution, and the temperature penalty factor ranged from 2.1-6.0 µg·(m3·â„ƒ)-1; a nonlinear correlation between O3-8h and RH was also observed, and O3-8h was the highest when RH was 55%. The sensitivity of different regions to Tmax and RH was slightly different; generally, the most suitable meteorological conditions for ozone formation were 29℃ ≤ Tmax< 38℃ and 40% ≤ RH<70%. In the Yangtze River Delta, Jiangsu-Anhui-Shandong-Henan, and the middle reaches of the Yangtze River, under extreme high temperature conditions (Tmax ≥ 35℃), O3-8h stopped increasing with the increase in temperature and even dropped; simultaneously, it was often accompanied with a small increase in particulate matter. It may be related to the heterogeneous reaction of some precursors with higher water vapor content and the increase in ozone heterogeneous sink.

[Seasonal Variations and Source Apportionment of Carbonaceous Components in Luoyang: Implication for Brown Carbon Contribution].

A total of 98 samples were collected to analyze the seasonal variation and source apportionment of carbonaceous components, especially brown carbon (BrC), of PM2.5in Luoyang during 2018-2019. The concentrations of organic carbon (OC) and elemental carbon (EC) ranged from (7.04±1.82) µg·m-3to(23.81±8.68) µg·m-3and (2.96±1.4) µg·m-3to (13.41±7.91) µg·m-3, respectively, showing the seasonal variation of being high in winter and low in summer; the carbonaceous fraction and secondary organic aerosol percentages were higher by 8.33%-141.03% and by 0.77%-63.14%, respectively, compared with that in 2015. The light absorption cross section (MAC) values showed different seasonal variations with the concentration of carbonaceous fraction, shown in descending order as autumn (7.67 m2·g-1)>winter (5.65 m2·g-1)>spring (5.13 m2·g-1)>summer (3.84 m2·g-1). The MAC values ranged from 3.84 to 7.67 m2·g-1 at 445 nm, which was lower than that in coal ash. Seasonal variation in light absorption and the contribution of BrC to total light absorption (babs,BrC,405 nm, babs,BrC,405 nm/babs,405 nm) in descending order was winter (31.57 Mm-1, 33%), autumn (11.40 Mm-1, 25%), spring (4.88 Mm-1, 23%), and summer (2.12 Mm-1, 21%). The proportion of carbonaceous components decreased as haze episodes evolved, whereas the contribution of light absorption of BrC increased, highlighting the important contribution of BrC to the total light absorption. The results of PMF and correlation coefficients of babs,BrC,405 nm and PM2.5 components indicated that motor vehicles and secondary nitrate contributed 27.7% and 24.0%, respectively. Our findings have significant scientific implications for the deep controlling of carbonaceous aerosol, especially for BrC, in Luoyang in the future.

Observational Insights into Isoprene Secondary Organic Aerosol Formation through the Epoxide Pathway at Three Urban Sites from Northern to Southern China.

Isoprene is the most abundant precursor of global secondary organic aerosol (SOA). The epoxide pathway plays a critical role in isoprene SOA (iSOA) formation, in which isoprene epoxydiols (IEPOX) and/or hydroxymethyl-methyl-α-lactone (HMML) can react with nucleophilic sulfate and water producing isoprene-derived organosulfates (iOSs) and oxygen-containing tracers (iOTs), respectively. This process is complicated and highly influenced by anthropogenic emissions, especially in the polluted urban atmospheres. In this study, we took a 1-year measurement of the paired iOSs and iOTs formed through the IEPOX and HMML pathways at the three urban sites from northern to southern China. The annual average concentrations of iSOA products at the three sites ranged from 14.6 to 36.5 ng m-3. We found that the nucleophilic-addition reaction of isoprene epoxides with water dominated over that with sulfate in the polluted urban air. A simple set of reaction rate constant could not fully describe iOS and iOT formation everywhere. We also found that the IEPOX pathway was dominant over the HMML pathway over urban regions. Using the kinetic data of IEPOX to estimate the reaction parameters of HMML will cause significant underestimation in the importance of HMML pathway. All these findings provide insights into iSOA formation over polluted areas.

[Characteristics of Water-soluble Ions in an Autumn Haze Process in the Southern Sichuan Urban Agglomeration After the Implementation of China's Air Pollution Prevention and Control Action Plan].

To investigate the PM2.5 pollution in the southern Sichuan urban agglomeration after the implementation of China's Air Pollution Prevention and Control Action Plan (APPCAP), PM2.5 samples were simultaneously collected in four cities (Neijiang, Zigong, Yibin, and Luzhou) from November 7 to 19, 2018. The pollution characteristics of PM2.5 and main water-soluble ions were analyzed in combination with the synoptic situation, and the influence of regional transport on atmospheric pollution was also discussed in this study. The results showed that the mean ρ(PM2.5) in this region was (67.2±38.3) µg·m-3, being highest in Luzhou and lowest in Neijiang. The proportion of SNA (SO42-, NO3-, and NH4+) in PM2.5 was 33.3%, among which NO3- was dominant. From the intermediate stage (2015) to the end(2018) of the implementation of APPCAP, ρ(PM2.5) values were increased by 13.8%, 47.2%, and 69.1% in Neijiang, Yibin, and Luzhou, respectively, though unchanged in Zigong. Due to the significant reduction in ρ(SO2) but slight decrease or increase in ρ(NO2), as well as the lack of controlling NH3 emissions, from 2015 to 2018, ρ(NO3-) had increased by 36.7%-116.0%, whereas ρ(SO42-) decreased by 19.8%-40.2%, and ρ(NH4+) changed slightly in four cities. On haze days, the nitrogen oxidation rate (NOR) increased by 60.0%-118.2%, whereas the sulfur oxidation rate (SOR) increased slightly or decreased, leading to a significant increase in ρ(NO3-) (2.7-3.0 times that on clean days) and NO3-/SO42- mass ratios (1.7-1.9 on haze days). These values indicated that the secondary formation of nitrate was the dominant chemical mechanism in this haze process. On haze days, the PM2.5 pollution in this region was mainly affected by the regional transport within Sichuan Basin, particularly by the northeasterly air masses passing through Chongqing.

[Characteristics of Water-soluble Inorganic Ions in PM2.5 in Beijing During 2017-2018].

To explore the characteristics of water-soluble inorganic ions (WSIIs) in PM2.5 during the process of continuous improvement of air quality in Beijing in recent years, a continuous collection of PM2.5 sample campaign was conducted in Beijing from 2017 to 2018. The PM2.5 mass concentration and WSIIs were then determined. The results showed that the average concentration of PM2.5 in Beijing was (77.1±52.1) µg ·m-3, with the highest and lowest values during spring [(102.9±69.1) µg ·m-3]and summer [(54.7±19.9) µg ·m-3], respectively. The average concentration of WSIIs was (31.7±30.1) µg ·m-3, accounting for 41.1% of the PM2.5 mass, and the seasonal contributions were: autumn (45.9%) > summer (41.9%) > spring (39.9%) ≥ winter (39.2%). SNA was an important component of the WSIIs that accounted for 86.0%, 89.5%, 74.6%, and 73.0% of the total WSIIs during spring, summer, autumn, and winter, respectively. With an increase in temperature, the concentration of NO3- increased initially and then decreased, while the concentration of SO42- increased. When the relative humidity was less than 90%, the concentrations of both NO3- and SO42- increased with an increase in relative humidity. With the aggravation of pollution, the overall contribution of WSIIs in PM2.5 increased significantly, and the evolution characteristics of different ions were different. Among them, the concentration and contribution of NO3- continued to increase, while the contributions of SO42- and the ions from dust (Mg2+, Ca2+, and Na+) decreased. During the observation period, the primary sources of WSIIs were secondary conversion, combustion source, and dust. The control of coal combustion and motor vehicles is critical to reduce the emission of WSIIs. The backward trajectory analysis showed that the air masses from the south and west of Beijing corresponded to the high PM2.5 concentration and proportion of WSIIs, and the contribution of secondary ions was significant. However, the concentrations and proportions of the air masses from the northwest and north were relatively low, but the contribution of Ca2+ was high.

[Characteristics of Carbonaceous Species in PM2.5 in Southern Beijing].

To investigate the characteristics of carbonaceous species in PM2.5 in Beijing after the implementation of the Action Plan for the Prevention and Control of Air Pollution, PM2.5 was continuously sampled in the heavily polluted southern urban area of Beijing from December 2017 to December 2018. The characteristics of organic carbon (OC) and element carbon (EC) were then determined. The results showed that the annual concentrations of PM2.5, OC, and EC in Beijing varied in wide ranges of 4.2-366.3, 0.9-74.5, and 0.0-5.5 µg ·m-3, respectively, and the average mass concentration were (77.1±52.1), (11.2±7.8), and (1.2±0.8) µg ·m-3. Overall, the carbonaceous species (OC and EC) accounted for 16.1% of the PM2.5 mass. The seasonal characteristics of the OC mass concentrations were: winter [(13.8±8.7) µg ·m-3] > spring [(12.7±9.6) µg ·m-3] > autumn [(11.8±6.2) µg ·m-3] > summer [(6.5±2.1) µg ·m-3]. The concentration of the EC during the four seasons was low, ranging from 0.8 to 1.5 µg ·m-3. The annual average mass concentration and contribution of secondary organic carbon (SOC) were (5.4±5.8) µg ·m-3 and 48.2%, respectively, highlighting the significant contribution of the secondary process. With the aggravation of pollution, although the contribution proportion of OC and EC decreased, their mass concentrations during "heavily polluted" days were 6.3 and 3.2 times that of "excellent" days, respectively. Compare to non-heating period, the mass concentrations of PM2.5, OC, and SOC increased by 14.4%, 47.9%, and 72.1% in heating period, respectively, which emphasized the importance of carbonaceous species during heating periods. Potential source contribution function (PSCF) analysis showed that the southwest areas of Beijing (such as Shanxi and Henan province) were the main potential source areas of PM2.5 and OC. The high value area of the PSCF of EC was less and the main potential source area was in the south of Beijing (such as Shandong and Henan province).

[Analysis of Stable Carbon Isotope Characteristics of PM2.5 in Summer and Winter Season in Xinxiang City].

We study the seasonal variations of δ13C ratios in aerosol fine particulate matter (PM2.5) using 91 PM2.5 samples collected from Xinxiang, China, during the summer and winter in 2017. Mass concentrations of total carbon (TC), water soluble ions, and stable carbon isotope ratios (δ13C) were determined. The mean concentrations of TC in the summer and winter were 11.78 µg·m-3 and 26.6 µg·m-3, respectively. The δ13C ratio in the summer ranged from -27.70‰ to -25.22‰. The daily δ13C ratio fluctuated in the first half of the summer months (mean -26.96‰), whereas the δ13C ratio in the second half of the summer was relatively stable (mean -25.69‰). The number of fires in the study area during the first half of the summer was quite different to the number during the second half of the summer, meanwhile, there was a positive correlation between the Knss+ concentration and the TC mass concentration (R2=0.62, P<0.01). This indicates that biomass burning most likely contributed to variations in δ13C. During the winter there was a significant negative correlation between winter RH and the TC/PM2.5 mass ratio (R2=0.68, P<0.01), which suggests that SOA growth was dominant in the early stage of haze development, whereas the pollution period was dominated by SIA components. The ratio of δ13C ranged from -26.72‰ to -23.49‰, and there was a difference between the variation of the δ13C ratio in haze episode (when it was mainly enriched in the development stage) to that in the stage dominated by depletion.

[Concurrent Measurement of Wet and Bulk Deposition of Trace Metals in Urban Beijing].

To characterize the dry and wet deposition of atmospheric trace elements in urban Beijing, both active and passive samplers were used to collect bulk and wet sedimentation samples between May 2014 and April 2015.The concentrations of 19 trace elements (Na, Mg, Al, K, Ca, V, Cr, Mn, Fe, Cu, Zn, As, Se, Mo, Cd, Sb, Tl, Th, and U) in the samples were analyzed by inductively coupled plasma mass spectrometry (ICP-MS). The results show that the concentrations of metals in bulk deposition samples[7160.68 µg·L-1 (Ca)-0.02 µg·L-1 (Th)] were generally higher than those in wet deposition samples[4237.74 µg·L-1 (Ca)-0.01 µg·L-1 (Th)], but the enrichment factors of each metal in the two kinds of samples were less different. Of note, the enrichment factors of Cu, As, Tl, Zn, Cd, Se, and Sb were all larger than 100, thus indicating that these heavy metals were mainly from anthropogenic sources. The statistical analysis of the air mass trajectory shows that the precipitation chemistry in urban Beijing is mainly affected by southward air flows. The air mass originating from the southwest region always had higher concentrations of Ca, Mg, Fe, Al, Cu, Mo, U, and Th, whereas the air mass from the south had higher concentrations of K, Zn, Mn, Sb, Cd, and Tl. During the observation period, the bulk deposition fluxes of metals varied from 3591.35 mg·(m2·a)-1 (Ca)-0.01 mg·(m2·a)-1 (Th), and wet deposition fluxes varied from 1847.78 mg·(m2·a)-1 (Ca)-0.01 mg·(m2·a)-1 (Th). The dry deposition fluxes of the 19 metals varied from 1743.57 mg·(m2·a)-1 (Ca)-0.01 mg·(m2·a)-1 (Th). The particle size has important implications in the evaluation of the relative importance of dry deposition versus wet deposition during the scavenging of trace elements in air.

[Concentration Characteristics and Source Analysis of PM2.5 During Wintertime in Zhengzhou-Xinxiang].

To study the pollution characteristics, sources, and transportation process of PM2.5 and its chemical compositions in the Zhengzhou-Xinxiang region, PM2.5 samples were collected using a middle volume sampler, in Zhengzhou and Xinxiang urban areas for 30 consecutive days during the winter of 2016. The mass concentration of PM2.5 was measured gravimetrically. 17 trace metals were determined by inductively coupled plasma-mass spectrometry (ICP-MS), and 7 water-soluble ions were determined by ion chromatography. The enrichment factor (EF) method and principal component analysis were employed to determine the source apportionment. The results showed that the daily mean PM2.5 mass concentration during the winter sampling period of 2016 in Xinxiang and Zhengzhou was 223.87 µg·m-3 and 226.67 µg·m-3, respectively, which indicated that pollution levels were relatively high in both cities. The concentration of three macro elements (Al, Ca, and Fe) accounted for 50% of the total metal elements in both cities, while the heavy metals concentration was higher in Xinxiang than in Zhengzhou. The EFs of Cd, Ag, and Pb in Xinxiang were far higher than 1000, while only Cd was higher than 1000 in Zhengzhou. NO3-, SO42-, and NH4+ were the main ions in the two cities. They exceeded 94% of total water-soluble ions and existed in the forms of (NH4)2SO4 and NH4NO3. The principle component analysis showed that the main contributors to PM2.5 were a mixture of biomass combustion and secondary aerosol in Xinxiang, and a mixture of coal combustion and traffic emissions in Zhengzhou, accounting for 34.94% and 33.99% of total PM2.5 emissions, respectively.

[Seasonal Variation and Source Analysis of Water-soluble Inorganic Ions in Fine Particulate Matter in Zhengzhou].

In order to explore the characteristics of PM2.5 concentration and water-soluble inorganic ions in Zhengzhou City, a total of 170 PM2.5 samples were collected in the spring, summer, autumn, and winter seasons of 2016, with 30 days continuous sampling during each season. The mass concentration of PM2.5 was analyzed gravimetrically, water-soluble inorganic ions were determined by ion chromatography, and principle component analysis was employed for source apportionment. The results showed that the mass concentration of PM2.5 was 150.72µg·m-3 during the sampling period. The mass concentration was highest in winter and lowest in summer, and that of autumn is higher was higher than that of spring. The ions SO42-, NO3-, and NH4+ were the major WSIs found in PM2.5, accounting for 92.55%, 92.94%, 93.06%, and 93.15% of the total amount of the seven ions found in spring, summer, autumn, and winter, respectively. The anion-to-cation ratio was 0.886, which indicated that PM2.5 was slightly alkaline in Zhengzhou. Secondary inorganic species, including NH4+, NO3-, and SO42- were the major components of the water-soluble ions. These ions most likely existed in the form of NH4NO3 and (NH4)2SO4 during spring and summer, while they were present as NH4NO3, (NH4)2SO4 and NH4HSO4 in autumn. In addition to these three forms, NH4Cl or other forms may exist in winter. Industrial emissions, combustion, secondary transformation, soil, and construction dust were the major sources of the water-soluble ions in PM2.5.

[Interannual Variation of Metal Elements and Water-Soluble Ions in PM2.5 During Wintertime in Xinxiang and Their Source Apportionment].

To study the interannual variations of chemical composition and source apportionment, a field campaign was carried out to collect the PM2.5 temperance sample during the winter of 2015 and the winter of 2016 in Xinxiang urban areas. PM2.5 mass concentration, metal elements, and the water-soluble ions were determined and meteorological factors were recorded simultaneously. The results showed that the daily mean concentrations of PM2.5 indicated serious pollution with values of 226 µg·m-3 and 224 µg·m-3 in 2015 and 2016, respectively. The Cd and Pb elements in PM2.5 were significantly enriched, with EF more than 1000. However, compared with 2015, the enrichment effect of most metal elements showed a trend of decrease in 2016. The water-soluble ions were mainly composed of SO42-, NO3-, and NH4+. The results showed a trade-off effect between metal elements and water-soluble ions in the two study periods. The results of PCA and PMF analyses show that there were four main emission sources in Xinxiang city in winter, namely dust, secondary source, industrial source, and fossil fuel combustion source. Moreover, the main sources of PM2.5 was the mixed source of soil and building dust and secondary aerosol pollution, with contributions of 37.46% and 34.94% in the winters of 2015 and 2016, respectively.

Variations of organic carbon storage in vegetation-soil systems during vegetation degradation in the Gahai wetland, China.

Qinghai-Tibet Plateau wetland, an important component of terrestrial ecosystem, plays an essential role in global carbon cycling. To understand the variation of organic carbon storage in vegetation-soil system during vegetation degradation in the Gahai wetland we examined aboveground litter, root biomass and soil organic carbon content in different degradation stages (CK: no degradation, SD: light degradation, MD: moderate degradation, HD: heavy degradation). The results showed that except for HD, carbon storage of aboveground biomass was 99.58-205.64 g·m-2 and that of root biomass (0-40 cm) was 56.96-754.37 g·m-2. The carbon stocks of aboveground and roots decreased significantly with degradation. Soil bulk density increased first and then decreased with degradation. Soil bulk density of each layer under degraded wetland was greater than that of the control. The carbon storage of litter was 17.29-35.69 g·m-2, which was significantly higher in CK than in MD and HD. The carbon storage in the soil (0-40 cm) was 7265.06-9604.30 g·m-2, with the order of MD＞CK＞SD＞HD. The carbon storage in CK and MD as significantly higher than that in SD and HD. The total carbon storage in the vegetation-soil system was 7265.06-10389.94 g·m-2 under different degradation stages. The largest was in CK, followed by MD, SD, and HD. Organic carbon was mostly stored in soil, which accounted for over 90% of the storage. Moderate interference might benefit carbon sequestration of the alpine wetland ecosystems.

[Mass Concentrations and Size Distributions of Water-soluble Inorganic Ions in Atmospheric Aerosols in Beibei District, Chongqing].

In order to study the concentration and distribution characteristics of water-soluble inorganic ions in aerosol particles of the Beibei district of Chongqing, aerosol samples were collected with an Andersen cascade impactor between March 2014 and February 2015. Water-soluble inorganic ions, including Na+, NH4+, K+, Mg2+, Ca2+, F-, Cl-, NO3-, and SO42- were determined for different particle sizes (9.00, 5.80, 4.70, 3.30, 2.10, 1.10, 0.65, and 0.43 µm) using the ion chromatography method. Results showed that SO42-, NH4+, NO3-, Cl-, Na+, and K+ were mainly distributed in fine particles, while Mg2+, Ca2+, and F- were mainly present in coarse particles. SNA (SO42-, NH4+, and NO3-) exhibited clear unimodal distribution, with peaks in the droplet mode of 0.65-1.10 µm, mainly present in the form of (NH4)2SO4 and NH4NO3 in fine particles. The formation of SO42- is mainly attributed to in-cloud processes and partly to oxidation of SO2. Na+, Cl-, and Mg2+ exhibited bimodal distribution in coarse and fine particles; K+ was a single peak distribution in the range of 0.43-1.10 µm, while peaks of F- and Ca2+ concentrations were in coarse particles. Average annual concentrations of total water-soluble ions in PM2.1 and PM9.0 were (32.68±15.28) µg·m-3and (48.01±19.66) µg·m-3 over the observation period. Seasonal variations of PM2.1 and PM9.0concentrations decreased in the order of winter > spring > summer > autumn. This was the same for most ions, but a small number of ions (F-, Mg2+ and Ca2+) had a different pattern in the spring, summer, and winter. The SNA were the major components of water-soluble ions in PM2.1, and Ca2+ was the major component of water-soluble ions in PM9.0 besides SNA. The concentration of cations was significantly higher than that of anions' in PM2.1 and PM9.0, with a certain correlation between different ions. Emissions from motor vehicle exhaust, combustion processes, soil sources, and fugitive dust were the major sources of water-soluble ions in this area. The effect of air temperature on secondary ions is significant (P<0.05), but relative humidity and wind speed have no significant effect (P>0.05).

[Particle Size Distribution and Human Health Risk Assessment of Heavy Metals in Atmospheric Particles from Beijing and Xinxiang During Summer].

Under a condition of good air quality (AQI:55-90, PM10:37-97 µg·m-3, PM2.5:17-76 µg·m-3), six groups of 54 samples were collected using an Andersen cascade impactor from both the indoor and outdoor stations in Beijing and Xinxiang from June to August in 2016. The samples were digested by microwave digestion, and nine heavy metal elements (Pb, Cr, Ni, Cu, Zn, As, Cd, Mn, and Co) in the atmospheric particles were determined with an inductively coupled plasma source mass spectrometer (ICP-MS). The results showed that the enrichment index (0-3) of most elements were low in both cities except for Cd[15.0 (Beijing) and 8.47 (Xinxiang)]. Cr, Co, Cu, and Mn in the atmospheric particles from Beijing park, Cd, Pb, and Mn in the atmospheric particles from the Beijing office, Cr, Co, Ni, and As in the atmospheric particles from Xinxiang park, and all nine heavy metal elements in the atmospheric particles from roads in both cities were found to be more concentrated in the coarse fractions; however, Pb, Zn, Cd, Ni, and As in the atmospheric particles from Beijing park, Co, Zn, Ni, Cr, As, and Cu in the atmospheric particles from the Beijing office, Pb, Zn, Cd, Cu, and Mn in the atmospheric particles from Xinxiang park, and all nine metal elements in the atmospheric particles from the Beijing office showed the opposite pattern. The result of a human health risk assessment indicated that the carcinogenic risk of the five carcinogenic elements were all less than 10-4, but a lower potential cancer risk would also occur under long term exposure. For the four non-carcinogenic elements (Pb, Zn, Mn, and Cu), the non-carcinogenic health risk values of Pb, Zn, Mn, and Cu in the atmospheric particulates in Beijing were all far less than 1, which means the corresponding non-carcinogenic risk was negligible; and, except for Mn, there was no obvious non-carcinogenic risk from Pb, Zn, and Cu in the atmospheric particles of Xinxiang.

[Seasonal Variation and Source Analysis of Water-soluble Inorganic Salts in PM2.5 in the Southern Suburbs of Beijing].

In order to study the variation of water-soluble inorganic ions in the four suburbs of Beijing using the atmospheric fine particulate matter rapid trapping system and chemical composition analysis system (RCFP-IC), we carried out measurements for nine water-soluble inorganic ions (Cl-, NO2-, NO3-, SO42-, Na+, NH4+, K+, Mg2+, Ca2+) in PM2.5 with continuous on-line observations for one year in Beijing's southern suburbs in 2016. The transport process of pollutants and the potential sources of pollutants were evaluated by combining a trajectory clustering method and potential source contribution factor analysis method (PSCF). During the observation period, the total concentration of the nine water-soluble inorganic ions was 38.6 µg ·m-3, and results showed that the concentration in winter and spring was high and in summer and autumn was low. The order of the concentration from high to low was SO42- > NO3- > NH4+ > Ca2+ > NO2- > Cl- > Na+ > K+ > Mg2+. In winter, the SO42-, NO3- and NH4+ accounted for 75.7% of the total measured water-soluble ions, followed by 72.8% in spring and 60.2% in summer. With an increase in air pollution, the concentrations of SO42-, NO3-, and NH4+ increased significantly, indicating that SO42-, NO3-, and NH4+ were closely related to the deterioration of air quality. SO42- was dominant in the formation of secondary ions compared to NO3- and NH4+; and SO42-, NO3-, and NH4+ had significant diurnal variations. The diurnal variation of the SO42- statistic (hours) was bimodal, and the peak values were at about 10:00 and 18:00. The diurnal variation of NO3- and NH4+ had single peaks, with the peak appearing at 10:00. The trend of the diurnal variation for these two ions was similar. Finally, the sources of pollution in the southern suburbs of Beijing mainly included secondary sources, coal-fired sources, and mixed sources of dust and dust. The main potential source of pollution in the southern suburbs was in the southeastern part of the observation site, while the northeastern airflow was favorable for the diffusion and dilution of pollutants.

[Pollution Characteristics of Organic Carbon and Elemental Carbon in Atmospheric Aerosols in Beibei District, Chongqing].

To study the pollution characteristics of atmospheric carbon aerosols, aerosol samples were collected via a cascade impactor (Andersen) from March 2014 to February 2015 in Beibei District, Chongqing. Organic carbon (OC) and element carbon (EC) were detected using a DRI 2001A carbon analyzer. The results showed that the annual average concentrations of OC and EC in PM2.1 were (16.3±7.6) and (1.8±0.7), respectively, and (25.0±9.6), and (3.2±1.3) µg·m-3, respectively, in PM9.0. The concentrations of both OC and EC were higher in winter and spring than in summer and autumn for PM2.1, whereas, for PM9.0, the concentration of OC was higher in summer and spring than in winter and autumn and that of EC was higher in winter and spring than in summer and autumn. The particle size distributions of OC and EC for the study year were analyzed, and it was found that those of OC were bimodal, with peaks in the size ranges of 0.43-0.65 µm for fine particles and 4.7-5.8 µm for coarse particles, and those of EC were trimodal, with peaks in the size ranges of 0.43-0.65 µm for fine particles and 4.7-5.8 µm for coarse particles and a concurrent significant peak in the particle size range of 2.1-3.3 µm. In addition, the correlations between OC and EC were analyzed and the SOC in PM2.1 was estimated. It was found that the average concentration of SOC was (6.3±5.9) µg·m-3, which accounted for 33.5%±22.6% of the OC concentration in Beibei District. Furthermore, OC and EC were significantly correlated. Finally, the pollution sources of atmospheric aerosols in Beibei were analyzed, and it was found that the pollution in Beibei mainly came from the exhaust gas of gasoline vehicles, biomass combustion, and coal combustion.

Significant Increase of Aromatics-Derived Secondary Organic Aerosol during Fall to Winter in China.

Human activities release large amounts of anthropogenic pollutants into the air, and thereby produce substantial secondary organic aerosol (SOA). Aromatic hydrocarbons (AHs) that mainly emitted from coal combustion, transportation, solvent use and biofuel/biomass burning, are a major class of anthropogenic SOA precursors. At present, there are few field studies focusing on AH-derived SOA (SOAA) on a continental scale, especially in polluted regions of the world. In this study, a one-year concurrent observation of the SOAA tracer, 2,3-dihydroxy-4-oxopentanoic acid (C5H8O5, DHOPA) was carried out at 12 sites across six regions of China for the first time. The annual averages of DHOPA among the 12 sites ranged from 1.23 to 8.83 ng m-3 with a mean of 3.48 ± 1.96 ng m-3. At all observation sites, the concentrations of DHOPA from fall to spring were significantly higher than those in summertime, and positive correlations were observed between DHOPA and the biomass burning tracer (levoglucosan). This indicated that such a nationwide increase of SOAA during the cold period was highly associated with the enhancement of biomass burning emission. In the northern China, the highest levels of DHOPA were observed in the coldest months during winter, probably due to the enhancement of biofuel and coal consumption for household heating. In the southern China, the highest levels of DHOPA were mostly observed in fall and spring, which were associated with the enhancement of open biomass burning. The apparent increases of DHOPA and levoglucosan levels during the cold period and the negative correlations of visibility with DHOPA and levoglucosan imply that the reduction of SOAA amount and biomass burning emission is an efficient way to reduce haze pollution during fall to winter in China.

[Atmospheric Dry Deposition Fluxes and Seasonal Variations of Particulate Matter and Lead in Urban Beijing].

To investigate the dry deposition pattern of particulate matter and lead in urban Beijing, dry deposited particles were collected based on a surrogate surface between December 2013 and November 2014 and subjected to elemental analysis by using microwave digestion and inductively coupled plasma mass spectrometry. The results showed that dry deposition fluxes of particle mass and total lead were 0.84 t·(hm2·a)-1 and 7.56 mg·(m2·a)-1, respectively, with a seasonal trend of spring > winter > autumn~summer, exhibiting a similar temporal pattern to that of coarse particles. In addition, dry deposition flux of water-soluble lead was 3.14 mg·(m2·a)-1. It was found that the ratio of soluble fraction to total lead in dry deposited particles reached up to 43%, coinciding with a seasonal variation of ambient sulfur dioxide. The findings highlighted the anthropogenic imprints on the dry deposition flux of particles and heavy metals as well as the solubility of lead. This study also provides a first-hand dataset that can be used to assess ecological and environmental impacts of dry deposited lead, and an up-to-date scientific basis for the crafting abatement strategies to further reduce emission of heavy metals in China.

[Characteristics of the Size Distribution of Water-soluble Ions During a Heavy Pollution Episode in the Winter in Tianjin].

To characterize the size distribution of water-soluble inorganic ions (WSⅡ) during a heavy pollution episode, particle samples were collected by an Andersen cascade sampler in Tianjin in January 2014, and the concentrations of eight WSⅡ (Na+, NH4+, K+, Mg2+, Ca2+, Cl-, NO3-, and SO42-) during a typical haze episode were analyzed by ion chromatography. The sources and formation mechanisms of WSⅡ were analyzed based on their size distributions. The results showed that the daily average concentrations of PM2.5 and PM10 were (138±100) µg·m-3 and (227±142) µg·m-3, respectively, and the average concentration of total WSⅡ concentrations (TWSⅡ) in the coarse and fine particles were (34.07+6.16) µg·m-3 and (104.16+51.76) µg·m-3, respectively. The concentrations of SO42-, NO3-, and NH4+ in the fine particles were much higher than concentrations of the other ions, and there were strong correlations between these three ions. The TWSⅡ on clear days, light pollution days, and heavy pollution days were (41.55±12.41) µg·m-3, (94.46±31.19) µg·m-3, and (147.55±27.76) µg·m-3, respectively. On clear days, SO42- showed a unimodal distribution, peaking at 0.43-0.65 µm; and NO3- showed a trimodal distribution, peaking at 0.43-0.65 µm, 2.1-3.3 µm, and 5.8-9.0 µm. NH4+ had a bimodal distribution, peaking at 0.43-0.65 µm and 4.7-5.8 µm. On heavy pollution days, however, the size distributions of these three secondary inorganic ions switched to a unimodal size distribution, peaking at 0.65-1.1 µm. Unimodal NH4+ mainly coexisted with SO42- and NO3-, and the excess NH4+ was found to be combined with Cl- in the fine particles. In the coarse particles, NH4+ completely coexisted with SO42- and NO3-.