Occurrence and seasonal variations of organophosphate flame retardants in air and dust from college microenvironments at Qingdao, China: Implications for student's exposure and risk assessment.

Organophosphate flame retardants (OPFRs) are widely used as alternatives to brominated flame retardants in a variety of consumer products and their consumption has continuously increased in recent years. However, their concentrations and human exposures in indoor microenvironments, particularly in a university environment, have received limited attention. In this study, the concentrations and seasonal variations of 15 OPFRs were assessed in typical microenvironments of two universities, including dormitories, offices, public microenvironments (PMEs: classroom, dining hall, gymnasium and library), and laboratories on the northern coast of China. Analysis of the OPFRs in both air and dust samples indicated widespread distribution in college campuses. The average concentration of ∑15OPFRs in the winter (12,774.4 ng/g and 5.3 ng/m3 for dust and air, respectively) was higher than in the summer (2460.4 ng/g and 4.6 ng/m3 for dust and air, respectively). The dust and air samples collected from PMEs and laboratories exhibited higher concentrations of OPFRs, followed by offices and dormitories. An equilibrium was reached between dust and air in all collected microenvironments. The daily intakes of OPFRs were significantly lower than the reference dose. Dust ingestion was the primary intake pathway in the winter, while inhalation and dust ingestion were the main intake pathways in the summer. The non-carcinogenic hazard quotients fell within the range of 10-7-10-3 in both the summer and winter, which are below the theoretical risk threshold. For the carcinogenic risk, the LCR values ranged from 10-10 to 10-8, indicating no elevated carcinogenic risk due to TnBP, TCEP, and TDCP in indoor dust and air.

[Characteristics, Sources Apportionment, and Health Risks of PM2.5-bound PAHs and Their Derivatives Before and After Heating in Zibo City].

Atmospheric polycyclic aromatic hydrocarbons (PAHs) and their derivatives are a global problem that influences the environment and threatens human health. To investigate the characteristics, sources, and health risk assessment of PM2.5-bound PAHs and their derivatives, PM2.5 were collected at an urban site in Zibo from November 5 to December 26, 2020, and the concentrations of 16 conventional PAHs, nine NPAHs, and five OPAHs in PM2.5 were analyzed using gas chromatography-mass spectrometry. Source apportionment of PAHs and their derivatives was conducted using diagnostic ratios and a PMF model, and the health risks of PAHs and their derivatives to adult men and women were evaluated using the source-dependent incremental lifetime cancer risk (ILCR) model. The results showed that the average concentrations of ∑16pPAHs, ∑9NPAHs, and ∑5OPAHs in PM2.5 of Zibo City during the sampling period were (41.61 ± 13.40), (6.38 ± 5.70), and (53.20 ± 53.47) ng·m-3, respectively. The concentrations of the three PAHs increased significantly after heating, which were 1.31, 2.04, and 5.24 times larger than those before heating. During the sampling period, Chr, BaP, and BaA were the dominant components of pPAHs; 9N-Ant and 2N-Flt + 3N-Flt were the dominant components of NPAHs; and ATQ and BZO were the dominant components of OPAHs. Source apportionment results showed that motor vehicles were the main source of PAHs and their derivatives in PM2.5 before heating, whereas after heating, the main sources were the mixed source of coal and biomass combustion and secondary formation. The total BaP equivalent (TEQ) was 14.5 ng·m-3 during the sampling period, and the TEQ increased significantly after heating, which was approximately 1.2 times of that before heating. Assisted by the individual PAH source apportionment results, the ILCR of PM2.5-boundPAHs and NPAHs in Zibo City had a certain potential carcinogenic risk for adult males (1.06 × 10-5) and females (9.32 × 10-6). Among them, the health risks of PAHs from gasoline vehicles, diesel vehicles, and coal/biomass combustion were significantly higher than those from other emission sources.

Distributions of PAHs, NPAHs, OPAHs, BrPAHs, and ClPAHs in air, bulk deposition, soil, and water in the Shandong Peninsula, China: Urban-rural gradient, interface exchange, and long-range transport.

A systematic study of the movement of PAHs (Polycyclic aromatic hydrocarbons) and their derivatives through air, soil, and water is key to understanding the exchange and transport mechanisms of these pollutants in the environment and for ultimately improving environmental quality. PAHs and their derivatives, such as nitrated PAHs (NPAHs), oxygenated PAHs (OPAHs), brominated PAHs (BrPAHs) and chlorinated PAHs (ClPAHs), were analyzed in air, bulk deposition, soil, and water samples collected from urban, rural, field, and background sites on the eastern coast of China. The goal was to investigate and discuss their spatiotemporal variations, exchange fluxes, and transport potential. The concentrations of PAHs and their derivatives in the air and bulk deposition displayed distinct seasonal patterns, with higher concentrations observed during the winter and spring and lower concentrations during the summer and autumn. NPAHs exhibited the opposite trend. Significant urban-rural gradients were observed for most of the PAHs and their derivatives. According to the air-soil fugacity calculations, 2-3 ring PAHs, BrPAHs, and ClPAHs were found to volatilize from the soil into the air, while 4-7 ring PAHs, OPAHs, and NPAHs deposited from the air into the soil. The air-water fugacity of the PAHs and their derivatives indicated that surface water was an important source for the ambient atmosphere in Qingdao. The characteristic travel distances (CTDs) and persistence (Pov) for atmospheric transport were much lower than that for the water samples, which may be due to the longer half-lives of PAHs and their derivatives in water. NPAHs and ClPAHs with long transport distances and strong persistence in water could lead to a significant impact on marine pollution.

The Levels of Polycyclic Aromatic Hydrocarbons and Their Derivatives in Plasma and Their Effect on Mitochondrial DNA Methylation in the Oilfield Workers.

This study focuses on the components and levels of polycyclic aromatic hydrocarbons (PAHs) and their derivatives (MPAHs and OPAHs) in plasma samples from 19 oil workers, pre- and post-workshift, and their exposure-response relationship with mitochondrial DNA (mtDNA) methylation. PAH, MPAH, OPAH, and platelet mtDNA methylation levels were determined using a gas chromatograph mass spectrometer (GC-MS) and a pyrosequencing protocol, respectively. The total plasma concentrations of PAHs in mean value were, respectively, 31.4 ng/mL and 48.6 ng/mL in pre- and post-workshift, and Phe was the most abundant (13.3 ng/mL in pre-workshift and 22.1 ng/mL in post-workshift, mean value). The mean values of total concentrations of MPAHs and OPAHs in the pre-workshift were 2.7 ng/mL and 7.2 ng/mL, while in the post-workshift, they were 4.5 ng/mL and 8.7 ng/mL, respectively. The differences in the mean MT-COX1, MT-COX2, and MT-COX3 methylation levels between pre- and post-workshift were 2.36%, 5.34%, and 0.56%. Significant (p < 0.05) exposure-response relationships were found between PAHs and mtDNA methylation in the plasma of workers; exposure to Anthracene (Ant) could induce the up-regulation of the methylation of MT-COX1 (ß = 0.831, SD = 0.105, p < 0.05), and exposure to Fluorene (Flo) and Phenanthrene (Phe) could induce the up-regulation of methylation of MT-COX3 (ß = 0.115, SD = 0.042, p < 0.05 and ß = 0.036, SD = 0.015, p < 0.05, respectively). The results indicated that exposure to PAHs was an independent factor influencing mtDNA methylation.

The association between internal polycyclic aromatic hydrocarbons exposure and risk of Obesity-A systematic review with meta-analysis.

Exposure to polycyclic aromatic hydrocarbons (PAHs) is emerging as a risk factor for obesity, but with conflicting findings. The aim of this systematic review is to investigate and summarize the current evidence towards the associations between PAHs exposure and risk of obesity. We conducted a systematic search of online databases, including PubMed, Embase, Cochrane Library, and Web of Science up to April 28, 2022. Eight cross-sectional studies with data from 68,454 participants were included. The present study illustrated that there was a significant positive association between naphthalene (NAP), phenanthrene (PHEN), and total OH-PAH metabolites and risk of obesity, the pooled OR (95% CI) was estimated at 1.43 (1.07, 1.90), 1.54 (1.18, 2.02), and 2.29 (1.32, 3.99), respectively. However, there was no significant association between fluorene (FLUO) and1-hydroxypyrene (1-OHP) metabolite and risk of obesity. Subgroup analyses showed that associations between PAHs exposure and risk of obesity were more apparent in children, female, smokers and developing regions.

Antibiotics and antimycotics in waste water treatment plants: Concentrations, removal efficiency, spatial and temporal variations, prediction, and ecological risk assessment.

For investigating the spatial, temporal variations and assessing ecological risk of 10 antibiotics and 6 antimycotics, influent sewage water and treated effluent were collected during three different seasons in 19 waste water treatment plants of Tianjin. High performance liquid chromatography tandem mass spectrometry was used to analyze 16 substances. The concentration range of influent samples was not detected (nd) -547.94 ng/L and the concentration range of effluent samples was nd-52.97 ng/L. By calculating the removal efficiency, it was found that Ciprofloxacin (CIP), Ofloxacin (OFL) and Clotrimazole (CTR) were effectively removed. There were significant spatial and temporal differences, the concentration in the dry season was evidently higher than that in the wet and normal seasons, and the northeast was lower than that in the northwest and southeast. By establishing a data set of influent and effluent, the priority features were extracted by feature engineering, which were temperature and NH3-N. Under the condition of ensuring the best performance of the models, the influent model with 9 features and the effluent model with 4 features were established, and the quantitative relationship between the above features and concentration was obtained through partial dependence analysis. Except for Moxifloxacin (MOX), Norfloxacin (NOR) and OFL in the influent samples, the RQ values for other antibiotics and antimycotics were less than 0.1. Among the effluent samples, only NOR had an RQ value greater than 0.1, and OFL, MOX, and Pefloxacin (PEF) had RQ values between 0.01 and 0.1. Comparing the observations and predictions individual RQ values, the predictions were ideal and matched the observations. This work effectively assessed environmental impact and provided a valuable reference for evaluating antibiotics and antimycotics ecological toxicity.

Association between mitochondrial DNA methylation and internal exposure to polycyclic aromatic hydrocarbons (PAHs), nitrated-PAHs (NPAHs) and oxygenated-PAHs (OPAHs) in young adults from Tianjin, China.

Polycyclic aromatic hydrocarbons (PAHs), nitrated-PAHs (NPAHs) and oxygenated-PAHs (OPAHs) are environmental pollutants with adverse effects on human health. The correlation between the concentrations of PAHs, NPAHs and OPAHs in human plasma and the methylation level of mitochondrial DNA (mtDNA) was investigated using data from 110 plasma samples collected in Tianjin, China. The median concentrations of PAHs, NPAHs and OPAHs were 16.0 (IQR: 14.4-20.7) ng/mL, 82.2 (IQR: 63.1-97.6) ng/mL and 49.6 (IQR: 28.6-53.8) ng/mL, and the mean proportions were 13.4%, 56.5% and 30.1%, respectively. Bisulfite-PCR pyrosequencing was used to measure the methylation level of MT-CO1 and tRNA-Leu. The methylation levels of two mitochondrial genes (MT-CO1, tRNA-Leu) including four CpG sites (MT-CO1-P1, MT-CO1-P2, tRNA-Leu-P1 and tRNA-Leu-P2) were 0.67% ± 1.38%, 13.54% ± 2.59%, 7.23% ± 5.35% and 1.64% ± 2.94%, respectively. To the best of our knowledge, this is the first time that significant correlations were found between PAHs and their derivatives exposure and mtDNA methylation levels.

[Agricultural Ammonia Emission Inventory and Its Distribution in Xining City].

Based on the field research activity level, the emission inventory of agricultural ammonia in Xining City in 2018 was established using the emission factor method. The emission characteristics of agricultural ammonia in Xining City were analyzed, a spatial grid distribution of 3 km×3 km was carried out by ArcGIS, and an uncertainty analysis of the ammonia emission inventory of livestock and poultry breeding and nitrogen fertilizer application was carried out via Monte Carlo simulation. The results showed that the total amount of ammonia emissions from agricultural sources in Xining City in 2018 was 4644.58 t. Among them, the total annual ammonia emissions from nitrogen fertilizer application and livestock and poultry farming were 1664.84 t and 2979.75 t, respectively, accounting for 35.84% and 64.16% of the total ammonia emissions from agricultural sources in Xining City. The spatial distribution results showed that the agricultural source ammonia emissions of Xining City mainly came from Datong County, Huangyuan County, and Huangzhong County, which accounted for 40.10%, 30.66%, and 28.05% of the total agricultural source ammonia emissions of Xining City, respectively. From the perspective of monthly distribution, no monthly difference in ammonia emissions was found in livestock and poultry farming. The ammonia emissions from nitrogen fertilizer application mainly existed in June (799.96 t) and July (768.48 t), accounting for 48.05% and 46.16% of the annual emissions. Monte Carlo simulation results showed that under a 95% confidence interval, the uncertainties of ammonia emissions from nitrogen fertilizer application agricultural source ammonia were low, ranging from -24.38% to 26.71%.

Fine particle-bound PAHs derivatives at mountain background site (Mount Tai) of the North China: Concentration, source diagnosis and health risk assessment.

Ten nitrated polycyclic aromatic hydrocarbons (nPAHs) and 4 oxygenated polycyclic aromatic hydrocarbons (oPAHs) in fine particulate matter (PM2.5) samples from Mount Tai were analyzed during summer (June to August), 2015. During the observation campaign, the mean concentration of total nPAHs and oPAHs was 31.62 pg/m3 and 0.15 ng/m3, respectively. Two of the monitored compounds, namely 9-nitro-anthracene (9N-ANT) (6.86 pg/m3) and 9-fluorenone (9FO) (0.05 ng/m3) were the predominant compounds of nPAHs and oPAHs, respectively. The potential source and long-range transportation of nPAHs and oPAHs were investigated by the positive matrix factorization (PMF) method and the potential source contribution function (PSCF) methods. The results revealed that biomass/coal burning, gasoline vehicle emission, diesel vehicle emission and secondary formation were the dominant sources of nPAHs and oPAHs, which were mainly from Henan province and Beijing-Tianjin-Hebei region and Bohai sea. The incremental life cancer risk (ILCR) values were calculated to evaluate the exposure risk of nPAHs and oPAHs for three group people (infant, children and adult), and the values of ILCR were 7.02 × 10-10, 3.49 × 10-9 and 1.41 × 10-8 for infant, children and adults, respectively. All these values were lower than the standard of EPA (Environmental Protection Agency) (<10-6), indicating acceptable health risk of nPAHs and oPAHs.

[Characteristics and Source Apportionment of Carbon Components in Road Dust in Anshan].

In order to study the characteristics and sources of carbon fractions in PM2.5 in road dust in Anshan, road dust samples were collected from nine roads in Anshan in October 2014 and re-suspended on filters using a NK-ZXF sampler to obtain PM2.5 samples. A thermal optical carbon analyzer (IMPROVE-TOR) was employed to measure the mass fraction of organic carbon (OC) and elemental carbon (EC) in PM2.5. The results showed that ω(TC) in PM2.5 in road dust was 9.78% (outer loop)-14.00% (Qianshan West Road), ω(OC) was 8.15% (outer loop)-10.84% (Qianshan West Road), and ω(EC) was 1.63% (outer loop)-2.85% (Qianshan West Road). ω(OC) was much higher than ω(EC), indicating that road dust contained a large amount of organic carbon. All OC/EC values were greater than 2.0 during the sampling period, suggesting that there was secondary pollution. Spearman correlation analysis and linear fitting indicated that the sources of OC and EC were basically the same. Cluster analysis results showed that carbon components in PM2.5 in road dust in Anshan mainly originated from vehicle exhaust, biomass burning, and coal combustion emissions.

Source apportionment and toxicity assessment of PM2.5-bound PAHs in a typical iron-steel industry city in northeast China by PMF-ILCR.

This study was designed to evaluate the occurrence and variation in concentrations, sources and cancer risk of PM2.5-bound PAHs. Airborne PM2.5-bound PAHs were sampled during a one-year campaign (2014-2015) in Anshan city, a typical iron and steel city in northeast China. A total of 374 PM2.5 samples were collected. A source-oriented positive matrix factorization (PMF) model and PAH diagnostic ratios were used to investigate the potential sources of PAHs in the atmospheric environment of Anshan, and the lifetime cancer risk of the population associated with PAHs through inhalation exposure was assessed by a PMF-ILCR model. Concentrations of PM2.5 and 16 PAHs ranged from 13.55 µg/m3 to 315.96 µg/m3 and 5.08 ng/m3 to 520.02 ng/m3, respectively. These values were higher in winter. PAH content from stationary sources and biomass combustion was higher than from other sources. Through the coefficient of divergence and localized PAH diagnostic ratio methods, we concluded that PM2.5-bound PAHs in Anshan originated mainly from the following sources: biomass combustion, vehicle emissions, fugitive dust, coking dust and natural gas emissions. Based on the source-oriented PMF model, coal combustion, fugitive dust, vehicle emissions, coking dust, and biomass combustion were the main sources contributing to PM2.5, accounting for 26.3%, 24.6%, 21.9%, 18.0%, and 6.3% of PM2.5, respectively. According to the PMF-ILCR model results, ILCR risks estimated for adults and children were respectively 1.19 × 10-5 and 8.55 × 10-6 in winter, higher than in other seasons, and higher than the threshold value (10-6). Together, vehicle emissions (diesel exhaust and gasoline exhaust), coal combustion and coking dust, contributed to over 86% of the cancer risk associated with PM2.5-bound PAHs exposure in Anshan.

[Characteristics and Source Apportionment of Carbon Components in Road Dust PM2.5 and PM10 During Spring in Tianjin Derived by Using the Quadrat Sampling Method].

In order to study the characteristics and sources of carbon fractions in PM2.5 and PM10 of road dust in Tianjin, samples of road dust were collected by the quadrat sampling method in April 2015 in Tianjin, and samples were re-suspended on filters by using a NK-ZXF sampler. A Thermal Optical Carbon Analyzer (IMPROVE-TOR) was employed to measure the concentrations of organic carbon (OC) and elemental carbon (EC), and the pollution characteristics and sources were investigated by non-parametric tests and OC/EC ratio, correlation, and cluster analyses. The results showed that ω(total carbon, TC) in PM2.5 of road dust amounted to 4.89% (secondary road) -18.83% (expressway), ω(OC) amounted to 3.57% (secondary road) -15.39% (expressway), and ω(EC) amounted to 1.32% (secondary road) -3.44% (expressway); meanwhile, ω(TC) in PM10 of road dust was 8.14% (secondary road) -19.71% (expressway), ω(OC) was 5.91% (secondary road) -16.28% (expressway), and ω(EC) was 1.96% (main road) -3.43% (expressway). The mass fraction of each carbon component for the expressway was relatively high, and that for the secondary trunk road was relatively low, which may have been due to the large traffic volume on the expressway and corresponding large amounts of exhaust emissions from motor vehicles, whereas there were fewer vehicles on the secondary trunk road. Additionally, ω(OC) was significantly larger than ω(EC) for all types of roads, and ω(EC) did not vary much among the different road types. The non-parametric tests of two related samples showed that there was no significant difference in the mass fraction of each carbon component between PM2.5 and PM10. The correlation analysis showed that the sources of OC and EC in road dust were roughly the same. The OC/EC ratio analysis and cluster analysis showed that the main sources of the carbon components in the dust of roads in Tianjin in spring were coal combustion, motor vehicle exhaust, and biomass burning.

Occurrence of heavy elements in street dust from sub/urban zone of Tianjin: pollution characteristics and health risk assessment.

Main purpose of this study was to determine the concentrations of selected heavy elements (As, Cd, Pb, Cu, Co, Cr and Ni) in the street dust samples (n = 49) collected from seven districts located in suburban/urban zone of Tianjin in order to estimate their possible sources and degree of environmental pollution as well as human health risk. Mean concentrations (mg kg-1) of As (19.3), Cd (0.60), Pb (28.4) and Cu (62.7) were above their corresponding soil background values. According to the results of multivariate statistical analysis, the accumulation of As, Cd, Pb, Cu and Cr in street dust was affected by anthropogenic activities, while the contents of Ni and Co were associated with natural sources. Pollution degree by geo-accumulation index had the following trend: Cd > Cu > As > Pb > Cr > Ni > Co. Dust contamination with Cd ranged from unpolluted to highly polluted. Potential ecological risk indicated low (Pb, Cu, Cr, Co and Ni) to high (Cd) risk, while potential risk index showed moderate and very high risks. Non-carcinogenic risk of the studied elements was below safe level (<1). Data obtained in this investigation gave the additional values to the knowledge needed for future monitoring and risk assessment, relating the presence of heavy elements studied in suburban/urban areas.

[Characteristics and Sources of Carbon Components in PM2.5 During Autumn and Winter in Panjin City].

In order to study the pollution characteristics and sources of carbon in Panjin City during autumn and winter, PM2.5 samples were collected at three monitoring points in October 2016 and January 2017. Pollution characteristics and sources of carbon components in PM2.5 were analyzed by the OC/EC ratio method, EC tracer method, and principal component analysis method. The results showed that the PM2.5 concentration exceeded the ambient air quality standard (GB 3095-2012) and that the average concentrations of OC and EC were 10.02 µg·m-3 and 3.91 µg·m-3 in autumn, respectively, and 16.04 µg·m-3 and 5.62 µg·m-3 in winter. According to the OC/EC ratio method, the OC/EC ratios were more than 2.0 during the sampling periods, indicating that there was secondary pollution in autumn and winter. Spearman correlation analysis and linear fitting indicated that the OC and EC sources were complex in development zones and that secondary school and cultural park areas may have similar sources during autumn and winter. SOC was quantitatively estimated by the EC tracer method, with concentrations of 7.21 µg·m-3 and 23.07 µg·m-3 in autumn and winter, respectively. The absolute and relative errors of SOC uncertainty were 0.98 µg·m-3 and 14.00% in autumn, respectively, and 1.87 µg·m-3 and 8.21% in winter. Based on the method of principal component analysis, the carbon components in autumn and winter were mainly derived from coal combustion, biomass burning, and vehicle exhaust.

[Characteristics of Elements in PM2.5 and PM10 in Road Dust Fall During Spring in Tianjin].

To explore the element pollution characteristics and sources of road dust fall, road dust fall samples were collected during spring in Tianjin and suspended to obtain PM2.5 and PM10, 16 elements were analyzed, and then their characteristics, sources, and similarities were studied by nonparametric tests, the coefficient of divergence, and enrichment factor. The results showed that the mass fraction (1%-20%) in sequential order of the elements in PM2.5 and PM10 in Tianjin road dust fall were Si > Al > Ca > Fe > Mg > K > Na. The coefficient of divergence of elements in PM10 and PM2.5 was 0.06, indicating that the elements profiles of PM10 might be similar to PM2.5. The elements of Cd and Cr in PM10 and PM2.5 were at a high level of enrichment degree, and Zn, Cu, Pb, and As showed significant enrichment. The main sources of the elements in PM10 and PM2.5 road dust fall in Tianjin were soil dust, construction dust, traffic dust (motor vehicle exhaust, tire wear, and brake wear), and coal combustion.

[Characteristics and Source Apportionment of Water-soluble Inorganic Ions in Road Dust PM2.5 During Spring in Tianjin Using the Quadrat Sampling Method].

In order to collect comprehensive information regarding the characteristics and sources of the water-soluble inorganic ions in road dust (RD) PM2.5 in Tianjin, samples of road dust were collected in April 2015 in Tianjin, and then re-suspended on filters using a NK-ZXF sampler. The concentrations of the major water-soluble inorganic ions were analyzed by ion chromatography. A correlation analysis, ratio method, and principal component analysis were used to analyze the sources of RD PM2.5. The results showed that the total water-soluble inorganic ion concentration in Tianjin accounted for 6.13%±2.32%, varying with different road types. Na+, K+, Mg2+, and Ca2+ showed high homology. NO3-/SO42- revealed that the main source of PM2.5 was mostly attributed to fixed sources. The principal component analysis showed that the main sources of RD PM2.5 in Tianjin were coal combustion, mobile sources, biomass burning, and construction dust.

[Characteristics and Source Apportionment of Water-soluble Ions in PM2.5 During Winter in Panjin].

In order to study the characteristics and source of water-soluble ions in PM2.5 in Panjin, PM2.5 samples were collected at three sites in January of 2017, and the levels of eight ions (Na+, Mg2+, Ca2+, K+, NH4+, SO42-, Cl-, and NO3-) were determined by ICS-900 ion chromatograph. The characteristics of PM2.5, the water-soluble ion concentration, SOR and NOR calculation, and ion balance calculation were investigated, and a principal component analysis was conducted. The results showed that the concentration of PM2.5 and water-soluble ions followed a descending sequence of park > development zone > the second middle school. SO42-, NO3-, and NH4+ were the major components of the water-soluble ions at the three sampling sites. SOR and NOR values were all higher than 0.10, indicating that SO42- and NO3- were mainly converted from SO2 and NOx. The ion balance calculation demonstrated that the cationic and anion equivalents in Panjin had great correlation in winter. Further study showed that the atmosphere in the development zone presented as neutral and that in the cultural park and the second middle school presented as partially alkaline. The principal component analysis further indicated that the water-soluble ions were mainly derived from fuel combustion, biomass burning, secondary particles, and re-suspended dust in winter.

PAEs occurrence and sources in road dust and soil in/around parks in May in Tianjin, China.

This is the first study reporting the presence of six phthalic acid esters (PAEs) in 45 composite soil and road dust samples collected in the urban zone of Tianjin, China. Three sample types (one soil and two road dust) were collected from the city parks. Soil samples (SI) were obtained from inside the park, road dust samples (RDI) were gathered from inside the park roads and the others (RDA) from roads surrounding parks. The range of concentrations of ∑6PAEs in SI, RDI and RDA were 0.07-0.92µgg-1, 0.42-6.32µgg-1 and 0.40-7.54µgg-1, respectively. The highest SI ∑6PAEs concentration (0.92µgg-1 in The People's Park) was 13 times higher than that of the lowest content (0.07µgg-1 in XiLiu Park). Furthermore, the spatial distribution of PAEs in RDI showed higher contents in the Nankai and Hexi districts. PAEs concentrations in different types of roads displayed significant differences (P < 0.05). The RDA PAEs distribution expressed decreasing order for different types of roads such as arterial road > sub-arterial road > branch road. The results of nonparametric tests on ∑6PAEs revealed significant differences between every two different sample types (P < 0.05). The analysis of the six PAEs types indicated DnBP and DEHP were the primary contaminating compounds in all sample types. The PCA results showed cosmetics and personal care products were important sources of PAEs in SI, and plasticizers were the key sources of PAEs in RDI and RDA.

Mycotoxins, trace elements, and phthalates in marketed rice of different origin and exposure assessment.

The aim of this study was to determine levels of 11 mycotoxins, 10 trace elements, and 6 phthalates in rice samples from Serbian and Chinese market. Mycotoxins were not detected in any of the analysed rice samples. Results revealed similar median levels for following elements: Mn, 17.5 and 15.7 mg kg-1; Fe, 2.47 and 2.12 mg kg-1; Cu, 1.95 and 1.59 mg kg-1 in marketed samples from Serbia and China, respectively. Median concentration of Ni in Serbian marketed samples was 1.9 times higher than in Chinese ones. The median levels (µg kg-1) of phthalates ranged from 1.2 (benzylbutyl phthalate [BBP]) - 566 (di(2-ethyl-hexyl) phthalate [DEHP]) and 1.7 (BBP) - 348 (DEHP) in Serbian and Chinese marketed samples, respectively. The results were used to assess daily exposure of Serbian and Chinese adult consumers. The calculated target hazard quotients indicated that the potential risk attributable to the analysed contaminants in rice samples should not be of concern neither for the Serbian nor the Chinese consumers.

[Characteristics and Source Apportionment of Water-soluble Inorganic Ions in Road Dust PM2.5 in Selected Cities in Liaoning Province].

In order to collect comprehensive information on the characteristics and sources of water-soluble inorganic ions in road dust (RD) PM2.5 in Liaoning Province, samples of road dust were collected in 2014 and 2016 in Anshan and Panjin and then re-suspended on filters using an NK-ZXF sampler. The concentrations of the major water-soluble inorganic ions were analyzed by ion chromatography. A correlation analysis, ratios, and a principal component analysis were used to analyze the sources of RD. The results showed that the total water-soluble inorganic ions in Panjin and Anshan accounted for 5.83%±3.34% and 5.84%±1.15% in RD PM2.5, respectively. NH4+, SO42-, and NO3- in RD PM2.5 coexisted in the forms of (NH4)2SO4, and NH4NO3 in Panjin, and NH4HSO4 and NH4NO3 in Anshan. The average values of NO3-/SO42- were 0.52±0.55 and 0.46±0.13 for Panjin and Anshan, respectively, indicating that the effects of stationary sources (e.g., coal combustion) on PM2.5 were more significant. The main sources of RD PM2.5 in Panjin were biomass burning, sea salt particles, construction dust, and mobile sources, while the main sources of RD PM2.5 in Anshan were coal combustion, biomass burning, sea salt particles, and steel smelting dust.