[Geochemical Background and Baseline Value of Soil Chemical Elements in Hebei Province].

Geochemical background and baseline values are important parameters for understanding the geochemical characteristics of soil elements, but the research degree of these two parameters is lacking in Hebei Province. Therefore, data from the multi-purpose regional geochemical survey and land quality geochemical assessment in Hebei Province from 2004 to 2018 were collected, covering approximately 71% of the land area of the whole province. Based on the data of surface soil and deep soil, scientific and robust methods including median value and median absolute deviation were used to calculate the geochemical background values, geochemical baseline values, as well as variation ranges of 54 indexes (Ag, Al2O3, As, Au, B, Ba, Be, Bi, Br, CaO, Cd, Ce, Cl, Co, Cr, Cu, F, Fe2O3, Ga, Ge, Hg, I, K2O, La, Li, MgO, Mn, Mo, N, Na2O, Nb, Ni, P, Pb, pH, Rb, S, Sb, Sc, Se, SiO2, Sn, Sr, Th, Ti, Tl, U, V, W, Y, Zn, Zr, total carbon (TC), and organic carbon (Corg)) in Hebei Province and 11 prefecture-level cities. The change rate in geochemical background for each index was also calculated. The results showed that the geochemical background and baseline values of most soil chemical elements in Hebei Province were lower than those nationwide, but the values of Ba, Br, Cl, MgO, Na2O, P, pH, S, Sr, and TC were higher, with CaO being the highest. Compared with those in north China, there was no significant difference in the geochemical background and baseline values for the 54 indexes, with the ratios of 0.83-1.17 and 0.79-1.19, respectively. Significant changes in the geochemical background for Corg, Hg, N, P, S, and Se were observed in Hebei Province, indicating that these indexes were greatly influenced by human factors. Preliminary analysis suggests that coal burning emissions and agricultural chemical use were two very important inducing factors.

[Changes in Concentrations and Pollution Levels of Trace Elements of Floodplain Sediments of Poyang Lake Basin in Recent Twenty Years].

Investigating the pollution conditions of trace elements in the Poyang Lake basin, identifying the pollution sources, evaluating the ecological risks play an important part in formulating the effective strategies for protecting the basin ecosystem. To understand the concentration characteristics, pollution levels, and ecological risks of twelve trace elements (Cd, Hg, Pb, As, Cu, Zn, Cr, Ni, Mn, Sb, W, and Sn) in the floodplain sediments of the five main tributaries in Poyang Lake basin in the past twenty years, we used the enrichment factor (EF) and modified pollution index (MPI) to quantify the pollution levels of the trace elements, and analyzed and discussed the pollution sources in the areas with significant pollution level changes. The results indicated that the concentrations of cadmium, zinc, manganese, tungsten and lead in the floodplain sediments of the Poyang Lake basin during the past twenty years have increased by 134%, 26%, 41%, 25%, and 8%, respectively, and mercury, arsenic, chromium, nickel, antimony, and tin have decreased by 35%, 15%, 22%, 10%, 14%, and 13%, respectively, while copper has not changed significantly. The concentrations of cadmium in the Raohe River, Ganjiang River, and Xinjiang River basins have increased by 331%, 151%, and 107%, while mercury decreased in the Fuhe River, Ganjiang River, and Xiushui River basins by 87%, 41%, and 40%, respectively. The classification results based on the EF indicated that the changes in the pollution levels of trace elements in the Poyang Lake basin were characterized by the aggravation of cadmium pollution and the degradation of mercury pollution, the pollution level of cadmium in the Ganjiang River basin was upgraded to moderate and significant, the pollution level of cadmium in the Le'an River was upgraded to very high, and the pollution level of mercury in the Fuhe River basin was reduced to unpolluted or minimal. The MPI classification results established that the increase in the cadmium pollution had intensified the comprehensive pollution in the Poyang Lake basin, causing the proportion of severely and heavily polluted sites to be raised from 17% to 33%. The MRI classification results also demonstrated that the proportion of very high ecological risk sites have increased from 11% to 22%. The element with the highest MRI contribution rate changed from mercury to cadmium, which was caused by the reduction of the ecological risk level from very high to moderate. The results demonstrated that the significant pollution changes in the trace elements in the floodplain sediments of the Poyang Lake basin were primarily caused by human activities, such as mineral exploitation, smelting, and industrial and agricultural production. Our findings can provide scientific evidence for the prevention and control of river pollution and the optimal management of a watershed ecosystem.

[Discussion on Key Issues of Geochemical Monitoring of Soil Heavy Metal in Xiong'an New District].

To build a soil environmental quality monitoring network and collect the systematic soil geochemical data of heavy metals before and after the construction of Xiong'an New District(XND), long-term variations in soil heavy metal levels during the XND construction were monitored based on the land quality geochemical survey monitoring data and the geochemical distribution of heavy metals. Parameters such as sampling density, sampling quantity, and sampling period were estimated to construct the geochemical monitoring network, which provides a reference for the future long-term monitoring of soil heavy metal geochemistry in XND. The results indicate that variations in the amount of heavy metals As, Cd, Cu, Hg, and Pb are greater than 36%, while the nugget coefficients of Cd, Cu, and Pb are greater than 75% because of the superposition of manmade sources on the high natural background levels. At the 95% and 90% confidence levels, while the allowable error Δ of the sample mean value is 5%, 10%, and 15% and heavy metals as As, Cd, Cu, Hg,Ni, Pb and Zn is monitored in soil environmental quality monitoring network, the proper numbers in the study area are 1077, 270, 120 and 767, 192, 86, respectively. The minimum detectable change(MDC)of each heavy metal species is between 0.0025 and 2.54 mg ·kg-1. Soil heavy metal monitoring requires different revisit intervals under different annual change rates, but in the study area, revisit intervals of soil monitoring are approximately two years under the current conditions of constant annual change rates.

[Ecological Risk Assessment of Heavy Metals at Township Scale in the High Background of Heavy Metals, Southwestern, China].

Heavy metals (HMs) are naturally occurring elements that have high natural background levels in the environment. Therefore, it is important to conduct ecological risk assessment and identify potential sources of HMs. In the past, studies were conducted at the regional scale. The accuracy of those studies could not meet the needs of spatial planning and natural resource management. Therefore, it is necessary to conduct ecological risk assessment at the township scale. In this study, 1092 soil samples (from 0-20 cm depth) were collected in the town of Reshui, an area with high background levels of soil HMs with the parent material of carbonatite, which is commonly found in Southwest China. The town of Reshui is a multi-ecological risk superimposed area where the ecological risk is high. In this study, concentrations of HMs (Cd, Cr, As, Hg, Pb, Cu, Zn, and Ni) in the topsoil were analyzed, and statistical analysis (SA), geographic information system (GIS) modeling, and positive matrix factorization (PMF) analysis were performed. The geoaccumulation index (Igeo) and potential ecological risk index (PERI) were applied for the ecological risk assessment and quantification of the sources of the soil HMs. The mean values of HM concentrations in the topsoil were 18.1, 1.18, 174.1, 202.2, 0.09, 71.1, 34.9, and 167.2 mg ·kg-1for As, Cd, Cr, Cu, Hg, Ni, Pb, and Zn, respectively, which were considerably higher than the average background value (ABV) in soils in Yunnan Province except for As and Pb. The average concentrations of Cd, Cr, Cu, and Ni exceeded the screening values specified in the soil contamination risk in agricultural land (GB 15618-2018) by 5.82, 1.16, 4.04, and 1.02 times, respectively. The Igeo value shows that the major pollutant is Cu in the surface soil of the study area, followed by Cr, and Cd. Speciation analysis of HMs indicates that HMs (Cr, As, Pb, Cu, Zn, and Ni) mainly exist in the residual form, mostly from the geological background with low bioavailability. The potential effective components of Hg have higher levels, but the total amount of Hg and its pollution risk are lower. Cd has a high bioavailability ratio, is easy to enter the soil solution and be absorbed by crops, and is the HM with the highest pollution risk in the study area. The PERI shows that the proportions of low ecological risk, moderate risk, and high risk soil samples are 44.23%, 54.40%, and 1.37% of the total number of samples, respectively. Hg and Cd were the major sources of risk because of their high toxicity coefficient. The PMF analysis indicates that there are four major sources of HMs in the study area: human activity, natural sources, coal mining and traffic emissions, and agricultural sources with the risk contribution ratios of 9.29%, 53.67%, 11.23%, and 25.81%, respectively. The PMF analysis effectively quantified the ecological risk from these sources, providing a reference for further pollution control and prevention measures.

[Trace Metals Pollution and Health Risks for Planning Area Soils of 193 Chinese Cities].

Urban soils are more easily subjected to modification, especially by contamination because of various human activities, and the environmental problems caused by urban soil pollution have become more prominent. To systematically investigate concentration characteristics, pollution levels, and exposure risks of 13 trace metals in urban soils of planning areas for 193 cities above the prefectural level, located in 31 provinces (autonomous regions and municipalities) of China, levels of pollution in urban soil were evaluated using the geoaccumulation index and integrated pollution index of trace metals, and health risks of residents exposed to urban soils were quantified using the health risk assessment method recommended by the US Environmental Protection Agency (USEPA). The results show that the median concentrations of As, Be, Cd, Co, Cr, Cu, Hg, Ni, Pb, Se, Tl, V, and Zn in topsoils of urban planning areas were 9.25, 2.14, 0.174, 12.4, 68.4, 28.2, 0.095, 27.7, 31.1, 0.29, 0.61, 82.7, and 82.2 mg·kg-1, respectively. Compared with the corresponding urban soil background values, the concentrations of Cd, Hg, and Se changed significantly. The geoaccumulation index (Igeo) values showed that Hg in urban soils of the planning area was the most severe pollutant, followed by Se and Cd, which caused pollution levels of uncontaminated to moderately contaminated levels, while other trace metals were uncontaminated. The Nemerow IPI (IPIN) revealed that the soils in 22 urban planning areas were heavily polluted and 16 urban planning areas were moderately polluted; in addition, the most polluted city in China was Zhuzhou in the Hunan province. The results of health risk assessment indicate that the soils in the five urban planning areas-Chenzhou City, Huangshi City, Zhuzhou City, Xiangtan City, and Longyan City-posed potential non-carcinogenic risks to children, and the major factor triggering risks was ingestion of Pb. To understand the soil pollution status and distribution of contaminated land parcel, it is suggested to carry out detailed investigation in cities with integrated moderate to heavy pollution to establish the list of contaminated land parcel and implement pollution control and restoration.

[Bioavailability, Translocation, and Accumulation Characteristic of Heavy Metals in a Soil-Crop System from a Typical Carbonate Rock Area in Guangxi, China].

This study uses 68 sets of paddy soil and rice grain samples collected from an area of carbonate rocks in Guangxi Province, China, to explore the ecological risks of heavy metals (As, Cd, Cr, Cu, Hg, Pb, Ni, and Zn) in soils from a high background area. We analyzed the concentrations of these heavy metals in soil and grain samples, and their chemical speciation in soil, and use these data to assess the associated ecological risks by means of statistics, a geo-accumulation index, bioconcentration factors (BCF), and correlation analysis. The arithmetic mean values of heavy metals concentrations in soil samples from the study area were (75.8±50.1), (1.91±1.02), (467.0±253.1), (48.5±9.8), (0.21±0.08), (76.2±28.1), (84.2±25.0), and (258.0±122.6) mg·kg-1 for As, Cd, Cr, Cu, Hg, Ni, Pb, and Zn, respectively, which were remarkably higher than of those from other regions within Guangxi Province and China. In comparison to China's soil environmental quality standard risk screening values (GB 15618-2018), the over-standard rates of Cd, As, and Cr were 95.6%, 86.8%, and 69.1%, respectively. In comparison to risk intervention values, the over-standard rates of Cd, As, and Cr were 27.9%, 17.6%, and 5.9%, respectively. Speciation analysis on heavy metals indicated that As, Cr, Cu, Ni, Pb, and Zn were mainly found in a residual form, and accounted for>80% of the total concentrations, and had a low bioavailability. The bioactive components (F1+F2+F3) of Cd accounted for 21%, and the bioactivity of Cd was higher than other elements. The potential bioavailable components (F4+F5+F6) of Hg accounted for 44%, with low total concentrations, which are understood to have little potential ecological harm for crops. However, the over-standard rates of Pb, Cd, and Cr in rice grains were only 23.5%, 8.8%, and 2.9%, respectively. Correlation analysis showed that there was no significant correlation between the concentrations of heavy metals in soils and the corresponding rice grains. The mean BCFs of each heavy metal were <0.1, and the BCFs of Hg, Pb, As, Cr, and Ni were <0.05. Overall, we found relatively high concentrations, low activity, and low ecological risks for heavy metals in the study area. For high geological background materials such as carbonate rocks, factors such as metal speciation, biological activity, and crop over-standard rates should be taken into account along with the traditional use of the total amount of heavy metals in a soil as the evaluation standard when formulating pollution control policies.

Biomonitoring of polycyclic aromatic hydrocarbons and synthetic musk compounds with Masson pine (Pinus massoniana L.) needles in Shanghai, China.

Twenty-six polycyclic aromatic hydrocarbons (PAHs) and four synthetic musk compounds (SMCs) accumulated by Masson pine needles from different areas of Shanghai were investigated in the present study. Concentrations of Σ26PAHs (sum of 26 PAHs) ranged from 234 × 10-3 to 5370 × 10-3 mg kg-1. Levels of Σ26PAHs in different sampling areas followed the order: urban areas (Puxi and Pudong) > suburbs > Chongming. Total concentrations of 16 USEPA priority PAHs ranged from 225 × 10-3 to 5180 × 10-3 mg kg-1, ranking at a relatively high level compared to other regions around the world. Factor analysis and multi-linear regression model has identified six sources of PAHs with relative contributions of 15.1% for F1 (vehicle emissions), 47.8% for F2 (natural gas and biomass combustion), 7.8% for F3 (oil), 10.6% for F4 (coal combustion), 15.7% for F5 ("anthracene" source) and 3.0% for F6 (coke tar). Total concentrations of 4 SMCs varied between 0.071 × 10-3 and 2.72 × 10-3 mg kg-1 in pine needles from Shanghai. SMCs with the highest detected frequency were Galaxolide and musk xylene, followed by musk ketone and Tonalide. The highest level of SMCs was found near industrial park and daily chemical plant. The results obtained from this study may have important reference value for local government in the control of atmospheric organic pollution.

Pine needles as biomonitors of polybrominated diphenyl ethers and emerging flame retardants in the atmosphere of Shanghai, China: occurrence, spatial distributions, and possible sources.

In this study, pine needles were used as biomonitors to investigate the levels, spatial distributions, and possible sources of polybrominated diphenyl ethers (PBDEs) and four emerging halogenated flame retardants (HFRs) in the atmosphere of Shanghai, China. The four emerging HFRs were hexabromocyclododecane (HBCD), decabromodiphenylethane (DBDPE), 1,2-bis(2,4,6-tribromophenoxy) ethane (BTBPE), and dechlorane plus (DP), with the first 3 HFRs being non-polybrominated diphenyl ether brominated flame retardants (non-PBDE BFRs). The total concentrations ranged from 3.71 to 4020 ng g-1 dry weight (dw) for 52 PBDE congeners (Σ52BDEs), < MDL (method detection limit) to 15.2 ng g-1 dw for three non-PBDE BFRs (Σ3non-PBDE BFRs), and 0.815 to 1090 pg g-1 dw for two DP isomers (ΣDP), respectively. High levels of PBDEs, three non-PBDE BFRs, and DP were found in pine needles from suburbs and Pudong, which was a consequence of industrial activities. The fraction of anti-DP isomer (fanti) in pine needles ranged from 0.515 to 0.939 with a mean value of 0.721, and most of the fanti values were consistent with those of technical DP formulations. Principal component analysis-multiple linear regression (PCA-MLR) model identified four sources of PBDEs in pine needles with the quantified contributions: degradation of technical PBDE formulations (49.5%), technical deca-BDE (6.9%), technical penta-BDE (25.1%), and technical octa-BDE (18.5%). These findings are expected to help understand the pollution level, fate, and possible sources of HFRs in the atmosphere of Shanghai and provide a basis for air pollution control and management in Shanghai.

Occurrence, sources, partitioning and ecological risk of short- and medium-chain chlorinated paraffins in river water and sediments in Shanghai.

The characteristics of regional environmental pollution of short- and medium-chain chlorinated paraffins (SCCPs and MCCPs) in river system from Shanghai were comprehensively investigated in this study for the first time. The total concentrations of SCCPs and MCCPs ranged from 15.0 to 1640 ng L-1 (median: 278 ng L-1) and 40.3 to 3870 ng L-1 (median: 939 ng L-1) in water, and from not detected (ND) to 2020 ng g-1 (median: 89.3 ng g-1) and 10.1 to 10,800 ng g-1 (median: 947 ng g-1) in sediments, respectively. The higher levels of SCCPs and MCCPs were found in water from Jinhui and Yexie rivers, and in sediments from Huangpu River, respectively. The concentrations of MCCPs were higher than those of SCCPs in both water and sediments, suggesting that the river system was mainly contaminated by MCCPs. Compared with other areas around the world, the concentrations of SCCPs and MCCPs were at medium to high levels in water and sediments. Factor analysis results revealed that SCCPs and MCCPs had different sources in both water and sediments. The log Koc values of CPs were significantly correlated with carbon chain lengths (p < 0.01), but not with chlorine number for both SCCPs and MCCPs (p > 0.05). A significant second-order polynomial relationship was observed between log Koc values and molecular weights of homologue groups of SCCPs (p < 0.001) and MCCPs (p < 0.01), respectively. SCCPs in water posed a low ecological risk at all sampling sites, and MCCPs in water posed a moderate ecological risk to aquatic life at nearly a fifth of sampling sites. SCCPs and MCCPs in sediments posed a low ecological risk to sediment dwelling organisms at most sampling sites.

Spatial variations, source apportionment and potential ecological risks of polycyclic aromatic hydrocarbons and synthetic musks in river sediments in Shanghai, China.

The aims of this study were to investigate the levels, possible sources and potential ecological risks of 26 polycyclic aromatic hydrocarbons (PAHs) including highly carcinogenic dibenzopyrene (DBP) isomers and 4 synthetic musks (SMs) in river sediments from Shanghai. 74 sediment samples were collected from the Huangpu River and its main tributaries. The total concentrations ranged from 52.0 to 11400 ng g-1 for Σ26PAHs, 25.1-9910 ng g-1 for 16 USEPA priority PAHs (Σ16PAHs), 0.769-384 ng g-1 for Σ4DBPs, and 0.080-63.3 ng g-1 for Σ4SMs, respectively. Seven sources of PAHs in river sediments were identified by positive matrix factorization (PMF) model. Coal combustion, vehicle and creosote were the major emission sources for PAHs. SMs came mainly from domestic and industrial wastewaters. The toxic equivalent quantities of the benzo[a]pyrene (TEQBaP) ranged from 7.64 to 3920 ng g-1 for Σ24PAHs, 2.07-1150 ng g-1 for Σ16PAHs, and 5.53-3150 ng g-1 for Σ4DBPs. The TEQBaP of Σ4DBPs made up 73.9% of Σ24PAHs, which indicated that DBPs were the major carcinogenic contributors to total PAHs in sediments. According to sediment quality guidelines (SQGs) and mean PEL-Q values, the risks posed by PAHs in sediments were at medium level at most sampling sites, and SMs posed a low ecological risk to sediment-dwelling organisms in Shanghai.

[Analysis of ecological risk and the content situation of polybrominated diphenyl ethers in sediments from Northeast China River Basin].

To investigate the polybrominated diphenyl ethers (PBDEs) pollution status, sediment samples were collected from major rivers in northeast China. Contents of 41 PBDEs congeners in sediments were measured using GC-NCI-MS. BDE209 was not detected, measured level of total PBDEs (excluding BDE209) ranged from 0.91 to 17.67 ng.g-1 dry weight, the highest concentrations of PBDEs were detected in the sediment samples from upstream and downstream of Jilin City in the Second Songhua River Basin, with 15.86 and 17.67 ng.g-1. BDE207 and BDE47 were the predominant PBDE congeners, with their concentrations accounting for 86. 5% and 76. 6% of the total PBDEs concentration measured in the samples. Each congener content difference was not obvious in other river sediments. PBDEs levels monitored in the present study were compared to those reported recently for districts located at home and abroad, and with ecological risk analysis. PBDEs content is at a low level in sediments of Northeast China River Basin and there is no ecological risk.

[Distribution characteristics and environmental significance of heavy metals in soil particle size fractions from tropical forests in China].

Three tropical forest soils were collected from Haikou, Qionghai and Tunchang in Hainan Island. Soil particle size fractionations were conducted using the standard dry-sieving procedure. Distribution of heavy metals in bulk samples and particle size fractions was determined by ICP-MS. The distribution characteristics and the response to organic carbon and iron were discussed. The results showed that the distribution of heavy metals was highly associated with the particle size fractions and variable patterns were found, which decreased with the increasing size. The accumulation of Cr, Ni, Cu, Zn, Cd and Cd was predominantly contributed by the particles finer than < 53 microm in diameter, whereas As mainly accumulated in particle size of 53-1 000 microm. Generally, the microaggregate (< 250 microm) contributed 14.38%-65.04% of heavy metals to the contents in bulk soil and the silt-clay aggregates (< 53 microm) contributed 2.61% -32.01%. The content of heavy metals except for As and Cd and Pb in Haikou soil in these different size fractions were controlled by the organic carbon and iron contents, which increased with the decreasing particle size.

Profile of organochlorine pesticides in soil cores from some hotspot areas of Beijing, China.

For the valid use of urban land and the safety of public health, an extensive contamination survey of organochlorine pesticides from five soil cores was conducted in the highly urbanized areas of Beijing in China. For topsoils in five soil cores, level of ∑HCHs and ∑DDTs varied from 0.174 to 4,783 ng g(-1) and 0.62 to 57,849 ng g(-1), respectively. The profile in topsoil of cores displayed that levels of pollutants in four soil cores from the urban areas with dense population are higher than that from outskirts. The depth characteristics of pollutants indicated that the level of ∑HCHs and ∑DDTs in BY and WU was close to/below the background value of soil in China (50 ng g(-1)), but those in some soil samples from A, B and ZX core, especially A and B, was above the threshold value for the soil safety (1,000 ng g(-1)). In views of the usage history of the land and profiles of contaminants, the source in A and B probably came from the dumped waste chemical materials in the old chemical factories. The study of soil cores sampled revealed the existence of chemical "time bomb" in urban regions of Beijing. Also, the finding indicated the absolute necessity of assessing the soil quality with the unprecedented land use changes in the big city community.

Mercury contamination in the topsoil and subsoil of urban areas of Beijing, China.

Mercury contamination is a serious problem in Chinese cities. In the present study, mercury contamination was evaluated in topsoil and subsoil samples collected in an urban area of Beijing. The level of total mercury in topsoil ranged from 12.1 to 8,487 ng g(-1), and a significant correlation (R = 0.58145, p < 0.0001) with polycyclic aromatic hydrocarbons was observed. Higher levels were generally observed in the suburbs and urban centers, with the highest levels being observed in the urban centers. The fraction of water soluble, ion exchangeable, Fe-Mn in the oxide-bound and organic phase was 0.78%, 0.18%, 0.25% and 3.42%, respectively. For subsoils, the level of total mercury ranged from 7.0 to 924.6 ng g(-1), and the higher levels were primarily located in the suburbs. This study showed that mercury has possibly affected the environmental quality of soil and groundwater in urban areas of Beijing.

Levels and distribution of organochlorine pesticides in various media in a mega-city, China.

As one of China's great metropolises, Taiyuan is generally recognized to be one of the most polluted cities in the world. It is affected by pollution from heavy industries, and from organochlorine pesticides (OCPs). In this study, we measured the concentrations of OCPs in various environmental media in Taiyuan. We measured the levels of OCPs in 15 soil samples and 34 samples of respirable particulate matter (PM) (17 of PM(2.5) and 17 of PM(10)) from urban areas of Taiyuan. Analysis of the composition ratios of OCP residues revealed that dichlorodiphenyltrichloroethane (DDT) and hexachlorocyclohexane (HCH) were the predominant compounds in soil, PM(2.5) and PM(10). The total DDT concentrations were 1.8-1.0x10(2)ngg(-1) in soil, 6.5-1.0x10(3)pgm(-3) in PM(2.5), and 8.5-1.5x10(3)pgm(-3) in PM(10). The total HCH concentrations were 1.4-45ngg(-1) in soil, 5.2-8.0x10(2)pgm(-3) in PM(2.5), and 9.6-8.7x10(2)pgm(-3) in PM(10). Furthermore, source analysis indicated that there was new input of OCPs at some sites. Finally, analysis of the individual OCPs revealed that new OCP contamination was the major problem in Taiyuan. This study suggests that measures should be taken to reduce the levels of OCP residues in order to improve the environmental quality in Taiyuan.

Spatial character of polychlorinated biphenyls from soil and respirable particulate matter in Taiyuan, China.

As one of China's great metropolises, Taiyuan is affected by heavy chemical industry and manufacture of chemical products, and faces pollution from polychlorinated biphenyls (PCBs). Therefore, this study was conducted to determine the PCB concentrations in various environmental media in Taiyuan. We collected 15 soil samples, 34 respirable particulate matter (PM) samples (17 of PM(2.5) and 17 of PM(10)) from urban areas of Taiyuan, and measured a total of 144 PCB congeners (including some coeluting PCB congeners). The total PCB concentrations were 51-4.7 x 10(3) pg g(-1) in soil, 27-1.4 x 10(2) pg m(-3) in PM(2.5) and 16-1.9 x 10(2) pg m(-3) in PM(10). Of the PCB homologues, the dominant PCBs detected in the various media were all tri-CBs. Soil was relatively the most polluted media. Furthermore, principal-component analysis revealed that the major PCB source in Taiyuan may be associated with the main commercial PCB through long-range transmission. Toxic equivalency (TEQ) concentrations (based on ten dioxin-like PCBs) ranged from N.D. to 5.9 x 10(-3) pg-WHO TEQ g(-1) in soil, 2.0 x 10(-4)-3.4 x 10(-3)pg-WHO TEQ m(-3) and 1.0 x 10(-4)-1.2 x 10(-3) pg-WHO TEQ m(-3) in PM(2.5) and PM(10), respectively. In previous studies, PCBs were not a severe component of contaminant in Taiyuan; however, this study suggested there is a potential threat of human exposure to PCBs for residents of Taiyuan.

Polycyclic aromatic hydrocarbon in urban soil from Beijing, China.

Polycyclic aromatic hydrocarbons (EPA-PAHs) in the urban surface soils from Beijing were determined using gas chromatography and mass spectrometry (GC-MS). It is significantly complementary for understanding the PAHs pollution in soil of integrated Beijing city on the basis of the information known in the outskirts. The total concentration of 16 EPA-PAH was from 0.467 to 5.470 microg/g and was described by the contour map. Compound profiles presented that the 4-, 5- and 6-ring PAHs were major compositions. The correlation analysis showed that PAHs have the similar source in the most sampling sites and BaP might be considered as the indicator of PAHs. Characteristic ratios of anthracene (An)/(An+ phenanthrene (Phe)), fluoranthene (Flu)/(Flu+ pyrene (Pyr)) and benzo [a]pyrene (BaP)/benzo [g,h,i]perylene (BghiP) indicated that the PAHs pollutants probably mainly originated from the coal combustion and it was not negligible from vehicular emission. The level of PAHs in our study area was compared with other studies.

Characterization of aliphatic hydrocarbons in deep subsurface soils near the outskirts of Beijing, China.

Thirty-nine deep subsurface soils (150-180 cm depth) near the outskirts of Beijing were investagated. The concentrations including n-alkanes from C13 to C36, pristane and phytane were in the range of 0.60 to 170.10 microg/g, with a median value of 4.26. Carbon preference index values for n-alkanes ranged from 1.08 to 2.98, with a median value of 1.48. The percentage contribution of "wax" n-alkanes was in the range of 6.03%--46.22%. A predominance of odd/even carbon n-alkanes and unresolved complex mixtures with different shapes and ranges were frequently observed. Factor analysis reduced the data set into three principal components and confirming contributions from low (19.58%), medium (20.49%) molecular weight species and long-chain n-alkanes (43.41%), respectively. Molecular biomarkers such as pristane, phytane, hopanes and steranes were detected. Based on the principal component analysis, the concentration profiles and molecular markers, it was found that the aliphatic hydrocarbons were from both biogenic and anthropogenic sources.