Preschool teachers' predicaments of teaching online and strategies employed during the COVID-19 pandemic: A literature review.

BACKGROUND: The COVID-19 pandemic accelerated the transition to remote preschool education, highlighting the crucial role of preschool teachers in navigating pedagogical transformations, adapting to technology, and addressing the challenges of distance learning. OBJECTIVE: This study delved into the intricate challenges confronted by educators specializing in early childhood education within the realm of remote instruction during the COVID-19 pandemic. Additionally, it scrutinized a spectrum of tactics and interventions implemented to overcome the challenges, presenting nuanced insights to enhance the effectiveness of online pedagogy. METHODS: Conducting a systematic literature review, this study comprehensively analysed academic sources to synthesize challenges faced by preschool teachers and their adaptive strategies during the transition to remote instruction induced by the COVID-19. The investigation focused on online teaching strategies, COVID-19 implications, and the broader landscape of remote learning. RESULTS: The review illuminated intricate challenges, encompassing technological constraints, pedagogical adjustments, and psychological adaptations. These challenges compelled the deployment of a diverse range of strategies, underscoring educators' resilience and resourcefulness in maintaining vibrant online teaching and learning ecosystems. CONCLUSION: This study offers a valuable compendium of insights, providing a comprehensive view of the evolving landscape of remote pedagogy. By fostering a nuanced understanding of the challenges and strategies, educators, administrators, and policymakers can collaboratively devise informed interventions. This collaborative effort optimizes online teaching practices, fostering enriched learning outcomes within the digital epoch.

[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.

[Concentration and Reactivity of Carbonyl Compounds in the Atmosphere of North China].

To reveal the characteristics of photochemical pollution in North China, adsorbing columns with 2, 4-dinitrophenylhydrazine(DNPH) were used to sample carbonyl compounds in Shijiazhuang and Xinglong between May 2018 and April 2019. The samples were analyzed by high-performance liquid chromatography to understand the composition, volume fraction, source, ·OH loss rate, and ozone formation potential of the carbonyl compounds. A total of 13 carbonyl compounds containing carbonyl groups were determined, of which acetone, formaldehyde, and acetaldehyde were highest at(6.46±5.25)×10-9, (3.76±2.29×10-9), and(2.65±1.74)×10-9 in Shijiazhuang compared to(1.85±1.27)×10-9, (1.29±1.02)×10-9, and(0.72±0.48)×10-9 in Xinglong, respectively. The estimated maximum ozone formation potential(OFP) of formaldehyde was much higher than that of acetaldehyde; the C1/C2 and C2/C3 ozone formation potential(OFP) of formaldehyde was much higher than that of acetaldehyde; and the C1/C2 and C2/C3 values showed that vehicle exhaust and fossil fuel combustion were the main sources in Shijiazhuang in association with the higher level of industrialization. In Xinglong, the carbonyl compounds mainly originated from natural sources. Acetaldehyde(1.77 s-1), formaldehyde(1.57 s-1), and butyraldehyde(0.42 s-1) contributed most to L·OH in Shijiazhuang, and formaldehyde(0.53 s-1), acetaldehyde(0.47 s-1), and butyraldehyde(0.12 s-1) were the three main contributors to L·OH in Xinglong. The carbonyl compounds contributing most to O3 production were formaldehyde and acetaldehyde at(34.61×10-9 O3) and (16.73×10-9 O3) in Shijiazhuang, compared to (11.77×10-9 O3) and (4.47×10-9 O3) in Xinglong, respectively.

Autophagy promotes oncolysis of an adenovirus expressing apoptin in human bladder cancer models.

As a potential cancer therapy, we developed a recombinant adenovirus named Ad-VT, which was designed to express the apoptosis-inducing gene (apoptin) and selectively replicate in cancer cells via E1a manipulation. However, how it performs in bladder cancer remains unclear. We examined the antitumor efficacy of Ad-VT in bladder cancers using CCK-8 assays and xenograft models. Autophagy levels were evaluated by western blotting, MDC staining, and RFP-GFP-LC3 aggregates' analyses. Here, we report the selective replication and antitumor efficacy (viability inhibition and apoptosis induction) of Ad-VT in bladder cancer cells. Using xenograft tumor models, we demonstrate that its effects are tumor specific resulting in the inhibition of tumor growth and improvement of the survival of mice models. Most Importantly, Ad-VT induced a complete autophagy flux leading to autophagic cancer cell death through a signaling pathway involving AMPK, raptor and mTOR. Finally, we suggest that treatment combination of Ad-VT and rapamycin results in a synergistic improvement of tumor control and survival compared to monotherapy. This study suggests that Ad-VT can induce selective autophagic antitumor activities in bladder cancer through the AMPK-Raptor-mTOR pathway, which can be further improved by rapamycin.

[Pollution Characteristics and Health Risk Assessment of Heavy Metals in PM2.5 Collected in Baoding].

To reveal the pollution characteristics and the health risks of the trace heavy metals in the atmospheric particles in Baoding, Hebei province, PM2.5 samples were collected using a middle volume sampler, and the mass concentrations of V, Cr, Mn, Co, Ni, Cu, Zn, As, Cd, and Pb in the samples were determined by microwave digestion-inductively coupled plasma-mass spectrometry (ICP-MS). The results showed that the PM2.5 concentration in Baoding ranged from 16.84-476.2 µg·m-3. During sampling, 65 samples were above the second-level standard of the Ambient Air Quality Standards (GB 3095-2012) by 54.2%. The most heavy metal elements showed higher levels in nighttime than during the daytime, except for except for Ni, Mn, and Co. Obvious seasonal variation was found with the trend of winter > autumn > spring > summer. The enrichment factors for Cu, Zn, Pb, and Cd were more than 1.5, indicating that those metals mainly came from anthropogenic emissions, such as traffic sources. Health risk assessment results indicated that the non-carcinogenic risk of heavy metals in PM2.5 in Baoding was small, and the carcinogenic risk resulting form As, Cr, Cd, and Co was greater for adults than for children.

Allium tuberosum alleviates pulmonary inflammation by inhibiting activation of innate lymphoid cells and modulating intestinal microbiota in asthmatic mice.

OBJECTIVE: This study tests whether long-term intake of Allium tuberosum (AT) can alleviate pulmonary inflammation in ovalbumin (OVA)-induced asthmatic mice and evaluates its effect on the intestinal microbiota and innate lymphoid cells (ILCs). METHODS: BALB/c mice were divided into three groups: phosphate buffer saline, OVA and OVA + AT. The asthmatic murine model was established by sensitization and challenge of OVA in the OVA and OVA + AT groups. AT was given to the OVA + AT group by oral gavage from day 0 to day 27. On day 28, mice were sacrificed. Histopathological evaluation of lung tissue was performed using hematoxylin and eosin, and periodic acid-Schiff staining. The levels of IgE in serum, interleukin-5 (IL-5) and IL-13 from bronchoalveolar lavage fluid (BALF) were measured by enzyme-linked immunosorbent assay. The ILCs from the lung and gut were detected by flow cytometry. 16S ribosomal DNA sequencing was used to analyze the differences in colon microbiota among treatment groups. RESULTS: We found that long-term intake of AT decreased the number of inflammatory cells from BALF, reduced the levels of IL-5 and IL-13 in BALF, and IgE level in serum, and rescued pulmonary histopathology with less mucus secretion in asthmatic mice. 16S ribosomal DNA sequencing results showed that AT strongly affected the colonic bacteria community structure in asthmatic mice, although it had no significant effect on the abundance and diversity of the microbiota. Ruminococcaceae and Desulfovibrionaceae were identified as two biomarkers of the treatment effect of AT. Moreover, AT decreased the numbers of ILCs in both the lung and gut of asthmatic mice. CONCLUSION: The results indicate that AT inhibits pulmonary inflammation, possibly by impeding the activation of ILCs and adjusting the homeostasis of gut microbiota in asthmatic mice.

Consumption of Lamb Meat or Basa Fish Shapes the Gut Microbiota and Aggravates Pulmonary Inflammation in Asthmatic Mice.

OBJECTIVE: In China, lamb and fish are well-known triggers for an asthma attack. Our investigation aims at assessing whether the long-term intake of lamb meat or Basa fish would aggravate pulmonary inflammation as well as exploring changes in the intestinal microbiota and immune cells in asthmatic mice. MATERIALS AND METHODS: The murine asthmatic model was established by intraperitoneal injection of ovalbumin (OVA) plus aluminum on day 0 and 14 and nebulization of OVA from day 21 to 27. Lamb meat or fish was administered to asthmatic mice by oral gavage from day 0 to 27. RESULTS: Our results showed that long-term consumption of lamb meat or Basa fish in asthmatic mice increased the number of inflammatory cells in bronchoalveolar lavage fluid (BALF), enhanced levels of IL-5, IL-13 in BALF and total IgE in serum, aggravated pulmonary inflammatory cell infiltration and mucus secretion. Long-term oral lamb enhanced the proportion of type 2 innate lymphoid cells (ILC2) from small intestine while it inhibited that of Treg from lung in asthmatic mice. Oral fish showed no remarkable effect on that of ILC2 from lung and small intestine but inhibited that of intestinal Treg in asthmatic mice. What's more, the chao-1 and observed species richness as well as PD whole tree diversity increased in asthmatic mice while these increments were inhibited after lamb treatment. PCA analysis indicated that there were significant differences in the bacterial community composition after lamb or fish treatment in asthmatic mice. Both lamb and fish treatment enhanced the abundance of colonic Alistipes in asthmatic mice. CONCLUSION: Collectively, long-term intake of lamb or fish shapes colonic bacterial communities and aggravates pulmonary inflammation in asthmatic mice, which provides reasonable food guidance for asthmatic patients.

Homoleptic alkynyl-protected gold nanoclusters with unusual compositions and structures.

We report two novel homoleptic alkynyl-protected gold nanoclusters, which were synthesized by direct reduction of AuC[triple bond, length as m-dash]CR. Single-crystal X-ray structural analysis reveals that they have compositions of Au42(C[triple bond, length as m-dash]CC6H4-2-CF3)22 (1) and Au50(C[triple bond, length as m-dash]C6H4-3-F)26 (2), respectively. Cluster 2 is the first Au50 nanocluster, and the metal-to-ligand ratios of 1 and 2 are different from those of known Aun(SR)m or Aux(C[triple bond, length as m-dash]CR)y nanoclusters. In addition, the metal kernels of these two clusters are built up unprecedented units. This work offers further insights into the synthesis of all-alkynyl-protected gold nanoclusters via a direct reduction method.

[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.

[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).

[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.

[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-.

[Characteristics of the Size Distribution of Water Soluble Inorganic Ions in Sanya, Hainan].

Size-resolved filter samples were collected in Sanya every other week from June 2012 to May 2014. The mass concentrations of water-soluble inorganic ions, including anions (Cl-, NO3-, SO42-) and cations (Na+, NH4+, K+, Mg2+, Ca2+) were measured by ion chromatography. The results showed that the total concentrations of measured water-soluble inorganic ions were (8.91±7.27) and (11.34±9.37) µg·m-3 in PM2.1 and PM2.1-9, respectively. In PM2.1, SO42- and NH4+ comprised 72.2% of all water-soluble inorganic ions, while in PM2.1~9, Cl-, Ca2+ and Na+ comprised 67.6% of all water-soluble inorganic ions. In PM2.1, the total concentrations of water-soluble inorganic ions had highest concentrations in winter and lowest concentrations in summer. In PM2.1~9, the total concentrations of water-soluble inorganic ions presented the highest concentrations in summer. SO42- and NH4+ showed bimodal size distributions and the peaks in the fine mode shifted from 0.43-0.65 µm in spring, summer and autumn to 0.65-1.1 µm in winter. NO3-, Na+, Cl-, Ca2+ and Mg2+ were unimodal with the peaks in the coarse mode of 4.7-9.0 µm. K+ showed bimodal size distribution with the fine mode at 0.43-0.65 µm and the coarse mode at 4.7-5.8 µm. PCA analysis showed that water-soluble inorganic ions were mainly affected by the secondary formation, sea salt and soil particles or falling dust.

[Concentration Characteristics and Sources of Trace Metals in PM2.5 During Wintertime in Beijing].

To study the characteristics and sources of trace metals in PM2.5 during wintertime in Beijing, PM2.5 samples were collected from December 2014 to January 2015 by a middle volume sampler in the urban area of Beijing for 30 consecutive days. The mass concentration of PM2.5 was measured by filter membrane weighting method, and 16 kinds of trace metals were determined by inductively couple plasma-mass spectrometry (ICP-MS). In addition, the pollution characteristics and sources of trace metals were analyzed by enrichment factor (EF) method and factor analysis, respectively. The results showed that the concentrations of five elements (i. e. K, Ca, Fe, Al and Mg) accounted for 90.7% of the total metal elements. The concentrations of the metal elements changed obviously between day and night. Compared with daytime, crustal elements like Mg and Al decreased by more than 30% while anthropogenic elements like Cu and Pb increased by more than 40% in nighttime. Although the concentrations of metal elements increased by nearly one time in heavy pollution days compared with clean days, the mass percent of which in PM2.5 decreased from 10.9% in clean days to 4.6% in heavy pollution days. This result suggested the accumulation of metal elements in heavy pollution days had a minor contribution to the increased mass concentration of PM2.5. As the pollution episode progressed, anthropogenic elements (Cu,Zn,As,Se,Ag and Cd) increased faster than crustal elements (Al,Mg,Ca,Mn and Fe), which showed ratios ranging from 2.9 to 5.3 for anthropogenic elements and ratios ranging from 1.2 to 1.8 for crustal elements, when compared between heavy pollution days and clean days. In addition, the EF value of anthropogenic elements was also increased in the pollution days, indicating the concentrations of these elements was further influenced by the anthropogenic sources. Factor analysis showed that metal elements of PM2.5 during wintertime of Beijing were mainly from coal combustion and biomass burning, motor vehicle and industry emissions, and re-suspension of road dust, with the contributions of 34.2%,25.5% and 17.1%, respectively.

[Comparison of Monitoring Methods of Organic Carbon and Element Carbon in Atmospheric Fine Particles].

Accurate measurement of organic carbon (OC) and elemental carbon (EC) in atmospheric fine particulate is an important scientific basis for studying the formation and source apportionment of carbonaceous aerosol. The selection of different analysis programs will lead to difference in the OC and EC concentrations, and further result in the misjudgment of the results. The OC and EC concentrations observed using three temperature protocols including RT-Quartz ( R) , NIOSH 5040 (N) and Fast-TC (F) were compared and analyzed in combination with the degree of air pollution in Beijing. The results showed that there was no significant difference in the TC (TC = OC + EC), OC and EC concentrations observed using R, N and F protocols and certain deviation was found among the TC (TC = OC + EC) , OC and EC concentrations. For TC, the results observed using R protocol were 5% lower than those using N protocol; hut 1% higher than those using F protocol. For OC, the results obtained using R were 9% lower than those using N protocol and 1% higher than those using F protocol. For EC, the results obtained using R were 20% higher than those using N protocol and 11% lower than those using F protocol. The variation coefficients for TC, OC and EC obtained based on R protocol were less than the other two temperature protocols under different air quality degrees. The slopes of regression curves of TC, OC and EC between on-line analysis using R protocol and off-line analysis were 1.21,1. 14 and 1.35, respectively. The correlation coefficients of TC, OC and EC were 0.99, 0.99 and 0.98, respectively. In contrast with the Black carbon ( BC) concentrations monitored by multi-angle absorption spectrophotometer (MAAP), the EC concentrations measured by on-line OC/EC analyzer using R protocol were obviously lower. When the BC concentrations were less than or equal to 8 gg*m3, the EC/BC ratio was 0.39. While the EC/BC ratio was 0.88, when the BC concentrations were greater than 8 ggm3. The variation trends of EC and BC concentrations were similar, while systematic error existed between the results obtained using those two instruments.

[Characteristics of the Size Distribution of Water Soluble Inorganic Ions During a Typical Haze Pollution in the Autumn in Shijiazhuang].

To characterize the size distribution of water soluble inorganic ions (WSⅡ) in haze days, particle samples were collected by an Andersen cascade impactor in Shijiazhuang from October 15 to November 14 in 2013, and the concentrations of eight kinds of WSⅡ (Na+, NH4+, K+, Mg2+, Ca2+, Cl-, NO3-and SO42-) during a typical haze episode were analyzed by ion chromatography. Sources and formation mechanism of WSⅡ were analyzed based on their size distributions. The results showed that Shijiazhuang suffers serious air pollution during the autumn season. The daily average concentrations of PM10and PM2.5were (361.2±138.7) µg·m-3 and (175.6±87.2) µg·m-3 and the daily average concentration of PM2.5was 2.3 times as high as the national secondary standard. The total water soluble inorganic ion concentrations (TWSⅡ) in clean days, light haze days and heavy haze days were(64.4±4.6)µg·m-3, (109.9±22.0)µg·m-3 and (212.9±50.1) µg·m-3 respectively. In addition, the ratio of secondary inorganic ions (SNA:SO42-, NO3- and NH4+) in TWSⅡ increased from 44.9% to 77.6% as changed from clean days to the heavy haze days, suggesting the evolution of haze episodes mainly originated from the formation and accumulation of SNA. The size distributions of SO42-, NO3- and NH4+ were bimodal in clean days, peaking at 0.43 -0.65 µm and 4.7-5.8 µm, respectively, which changed to unimodal distribution in both the light and heavy haze days, peaking at 0.65-1.1 µm. Owing to high humidity during the heavy haze days, the aqueous phase reactions of SO42- and NO3- were likely promoted, which led to the transformation of condensation mode in clean days to the droplet mode in haze days. The size distributions of Na+, Mg2+ and Ca2+ were different with that of SNA, which showed a coarse mode peaking at 4.7-5.8 µm both in clean and haze days, whereas K+and Cl- showed a bimodal distribution both in clean and haze days, although the modal size was different in clean and haze days.

[Characteristics of Winter Atmospheric Mixing Layer Height in Beijing-Tianjin-Hebei Region and Their Relationship with the Atmospheric Pollution].

Atmospheric mixing layer height (MLH) is one of the main factors affecting the atmospheric diffusion and plays an important role in air quality assessment and distribution of the pollutants. Based on the ceilometers data, this paper has made synchronous observation on MLH in Beijing-Tianjin-Hebei region (Beijing, Tianjin, Shijiazhuang and Qinhuangdao) in heavy polluted February 2014 and analyzed the respective overall change and its regional features. Results show that in February 2014,the average of mixing layer height in Qinhuangdao is the highest, up to 865 +/- 268 m, and in Shijiazhuang is the lowest (568 +/- 207 m), Beijing's and Tianjin's are in between, 818 +/- 319 m and 834 +/- 334 m respectively; Combined with the meteorological data, we find that radiation and wind speed are main factors of the mixing layer height; The relationship between the particle concentration and mixing layer height in four sites suggests that mixing layer is less than 800 m, concentration of fine particulate matter in four sites will exceed the national standard (GB 3095-2012, 75 microg x m(-3)). During the period of observation, the proportion of days that mixing layer is less than 800 m in Beijing, Tianjin, Shijiazhuang and Qinhuangdao are 50%, 43%, 80% and 50% respectively. Shijiazhuang though nearly formation contaminant concentration is high, within the atmospheric mixed layer pollutant load is not high. Unfavorable atmospheric diffusion conditions are the main causes of heavy pollution in Shijiazhuang for a long time. The results of the study are of great significance for cognitive Beijing-Tianjin-Hebei area pollution distribution, and can provide a scientific reference for reasonable distribution of regional pollution sources.

[Composition characteristics of atmospheric volatile organic compounds in the urban area of Beibei District, Chongqing].

In order to study the composition and distribution of VOCs (Volatile Organic Compounds) in the atmosphere in the urban area of Beibei district, Chongqing, atmospheric samples were collected from March 2012 to February 2013 with special stainless steel cylinders, and analyzed with a three-stage preconcentration method coupled with GC-MS. 78 species of VOCs were detected in this study, of which there were 25 species of alkanes, 15 species of olefins, 28 species of aromatic hydrocarbons and 10 species of halogenated hydrocarbons. The results showed that the top seven species of VOCs according to the order of annual average concentration in the atmosphere of Beibei were: Dichloromethane (3. 08 x 10(-9) ) , Benzene (2. 09 x 10-9) , Isopentane (1. 85 x 10 -9) , Toluene (1. 51 x 10(-9)) , Propane (1. 51 x 10(-9)), m/p-xylene (1.43 x 10(-9)) and Styrene (1. 39 x 10-9). The concentration of TVOCs (Total Volatile Organic Compounds) in the atmosphere of Beibei was 33. 89 x 10 -9 during the measuring period, and the seasonal variation was obvious with the order of spring (42. 57 x 10 -9) > autumn (33.89 x 10-9) > winter (31.91 x 10 -9) > summer (27.04 x 10(-9)). In the composition of TVOCs, alkanes and aromatic hydrocarbons provided the largest contribution to TVOCs (31.5% and 30.7% ) , followed by halogenated hydrocarbon, accounting for 27.4% , and the last one was olefins, with only 10.4%. By means of ozone formation potential, the analysis results showed that olefins and aromatic hydrocarbon compounds were the two important materials which made the biggest contribution to the formation of ozone in the atmosphere of Beibei. We further analyzed the sources of VOCs in atmosphere of Beibei by the method of Principal Component Analysis (PCA). Vehicle exhaust was the biggest source and its contribution to VOCs was 50. 41%. The calculated results with T/B value also confirmed that traffic was the biggest source contributing to the VOCs in atmosphere of Beibei.

[Size distributions of water-soluble inorganic ions in atmospheric aerosols in Fukang].

To investigate the levels and size distributions of water soluble inorganic components, samples were collected with Andersen cascade sampler from Feb. 2011 to Feb. 2012, in Fukang, and were analyzed by IC. The variation trend, concentration level, composition, sources and size distribution of major ions during non-heating period were compared with heating period. Based on the specific samples, ionic compositions and size distributions were analyzed during heavy pollution, straw burning and spring planting periods. The results showed that inorganic components in Fukang were severely affected by heating. The total water soluble ions in fine and coarse particles during non-heating and heating periods were 11.17, 12.68 microg x m(-3) and 35.98, 22.22 microg x m(-3), respectively. SO4(2-) was mainly from saline-alkali soil, NO3(-) and NH4(+) were from resuspension of farmland soil during non-heating period, while SO4(2-), NO3(-) and NH4(+) were all from the fossil fuel consumption during the heating period. All ions were bimodal distribution during non-heating and heating periods. During the heating period, the particle size growth of SO4(2-), NO3(-) and NH4(+) in fine mode was found, SO4(2-) and NH4(+) peaked at 3.3-4.7 microm in coarse particles. Secondary pollutions were serious during heavy pollution days with high levels of secondary ions between 1.1 and 2.1 microm. Biomass burning obviously affected the size distribution of ions during the straw burning period and ions focused on smaller than 0.65 microm, while there were more soil dusts during spring planting periods and ions concentrated in larger than 3.3 microm.

[Observation of atmospheric pollutants in the urban area of Beibei District, Chongqing].

To study the characteristics of atmospheric pollutants in the urban area of Beibei district of Chongqing, the concentrations of the atmospheric pollutants were measured by automatic on-line continuous monitoring equipments from Jan. 2012 to Feb. 2013. The results showed that the concentrations of the pollutants often exceeded the corresponding values of the new National Ambient Air Quality Standards (GB 3095-2012) except SO2. Of these pollutants, PM2.5 was the most serious in this area. The concentrations of the atmospheric pollutants had significant seasonal variation. The concentrations of O3 and O(x) were both the highest in summer and the lowest in winter. The average concentrations of O3 were (36.1 +/- 19.2), (48.8 +/- 32.6), (29.8 +/- 28.6) and (18.2 +/- 15.8) microg x m(-3), and the average O(x) concentrations were (77.6 +/- 20.6), (91.3 +/- 37.6), (77.5 +/- 30.6) and (69.4 +/- 18.2) microg x m(-3) in spring, summer, autumn and winter in 2012, respectively. The concentrations of NO(x) appeared higher in winter and lower in summer, the average concentrations of NO, NO2 and NO(x) were (11.8 +/- 9.4), (42.3 +/- 13.1) and (54.1 +/- 20.8) microg x m(-3) in spring, (8.2 +/- 4.9), (40.5 +/- 9.9) and (48.7 +/- 12.6) microg x m(-3) in summer, (20.7 +/-17.1), (47.2 +/- 14.1) and (67.9 +/- 25.5) microg x m(-3) in autumn, and (30.4 +/- 25.1), (51.2 +/- 15.9), (81.6 +/- 37.9) microg x m(-3) in winter. The concentrations of SO2 appeared higher in spring and winter, and lower in summer and autumn. The concentrations of SO2 were (50.5 +/- 23.3), (26.3 +/- 16.7), (38.8 +/- 18.4) and (53.7 +/- 23.4) microg x m(-3) in spring, summer, autumn and winter, respectively. The concentrations of PM2.5 appeared higher in winter and changed smoothly in other seasons, with the average concentration of (61.4 +/- 28.5), (68.1 +/- 32.5), (61.9 +/- 27.1) and (89.6 +/- 44.2) microg x m(-3) in spring, summer, autumn and winter, respectively. The curves of diurnal variations of O3, O(x), NO, NO(x) and SO2 all showed single peak. However, the time of the peak values varied for different pollutants, 16:00 for O3 and O(x), and 8:00-11:00 for NO, NO(x) and SO2. The diurnal variations of NO2 and PM2.5 were similar to the two peaks that appeared in the morning and at night, respectively. Moreover, the diurnal ranges of O3 and O(x) concentrations were much wider in summer, while the wider ranges were observed in winter for NO, NO2, NO(x), SO2 and PM2.5. There was no difference in the diurnal pattern of NO between weekends and weekdays, the concentrations of N2O in weekdays were much higher than those on weekends, but with O3 the situation was the opposite. Correlation analysis indicated that the O3 concentration was positively correlated with temperature and wind speed, while negatively correlated with relative humidity. However, the situation of NO(x) was the opposite. PM2.5 concentration was negatively correlated with temperature and wind speed, while positively correlated with relative humidity. SO2 concentration had different correlations with the meteorological parameters in different seasons. In addition, wind direction was an important factor affecting the concentrations of the atmospheric pollutants.