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Surface soil and river sediment samples were collected from the downstream of Chuhe River basin, East China, to investigate the occurrence and accumulation characteristics of legacy and novel brominated flame retardants (NBFRs). The respective concentrations of BDE-209 and nine NBFRs ranged from n.d. to 41.4 ng/g dry weight (dw) and from 0.35 to 362.78 ng/g dw in the collected surface soil samples and ranged from 0.29 to 19.73 ng/g dw and from 0.70 to 66.83 ng/g dw in the collected river sediment samples. Soil samples exhibited a higher potential to accumulate BTBPE while the relative abundance of PBT in the collected sediment samples was significantly higher than that in soils. Even so, BTBPE was the predominant NBFR in both soil and sediment samples. The concentrations and relative abundances of legacy and NBFRs exhibited large spatial variation. The calculated concentration ratios of the total of the nine NBFRs (∑9NBFRs) to BDE-209 (∑9NBFRs/BDE-209) in most of the analyzed samples far exceeded 1, implying a clear shift from legacy brominated flame retardants to NBFRs in the downstream of Chuhe River basin. [ABSTRACT FROM AUTHOR]

Novel brominated flame retardants (NBFRs) and dechlorane plus (DP) have been widely used as alternatives to traditional BFRs. However, little is known about the temporal trends of NBFR and DP pollution in e-waste recycling sites. In the current study, three composite sediment cores were collected from an e-waste-polluted pond located in a typical e-waste recycling site in South China to investigate the historical occurrence and composition of NBFRs and DP. The NBFRs and DP were detected in all layers of the sediment cores with concentration ranges of 5.71~180,895 and 4.95~109,847 ng/g dw, respectively. Except for 2,3,5,6-tetrabromo-p-xylene (pTBX) and 2,3,4,5,6-pentabromoethylbenzene (PBEB), all the NBFR compounds and DP showed a clear increasing trend from the bottom to top layers. These results implied the long-term and severe contamination of NBFRs and DP. Decabromodiphenyl ethane (DBDPE) was the most abundant NBFR with the contribution proportions of 58 ± 15%, 73 ± 15%, and 71 ± 18% in three sediment cores, followed by 1,2-bis(2,4,6-tribromophenoxy) ethane (BTBPE) and pentabromobenzene (HBB). The ratios of BTBPE/Octa-BDEs and DBDPE/Deca-BDEs varied from 0.12 to 60 and from 0.03 to 0.49, respectively, which had no clear increase trends with a decrease in sediment depth. As for DP, the fanti values (the concentration ratios of anti-DP to the sum of anti-DP and syn-DP) in sediment cores ranged from 0.41 to 0.83, almost falling in the range of those in DP technical products, suggesting that DP degradation did not occur in sediment cores. The environmental burdens of DBDPE, BTBPE, HBB, PBT, PBEB, pTBX, and DP were estimated to be 34.0, 5.67, 10.1, 0.02, 0.02, 0.01, and 34.8 kg, respectively. This work provides the first insight into the historical contamination status of NBFRs and DP in the sediments of an e-waste recycling site. [ABSTRACT FROM AUTHOR]

Organophosphate esters (OPEs) are frequently used as flame retardants and plasticizers in various commercial products. While initially considered as substitutes for brominated flame retardants, they have faced restrictions in some countries due to their toxic effects on organisms. We collected 37 soil and crop samples in 20 cities along the coast of South China, and OPEs were detected in all of them. Meanwhile, we studied the contamination and potential human health risks of OPEs. In soil samples, the combined concentrations of eight OPEs varied between 74.7 and 410 ng/g, averaging at 255 ng/g. Meanwhile, in plant samples, the collective concentrations of eight OPEs ranged from 202 to 751 ng/g, with an average concentration of 381 ng/g. TDCIPP, TCPP, TCEP, and ToCP were the main OPE compounds in both plant and soil samples. Within the study area, the contaminants showed different spatial distributions. Notably, higher OPEs were found in coastal agricultural soils in Guangdong Province and crops in the Guangxi Zhuang Autonomous Region. The results of an ecological risk assessment show that the farmland soil along the southern coast of China is at high or medium ecological risk. The average non-carcinogenic risk and the carcinogenic risk of OPEs in soil through ingestion and dermal exposure routes are within acceptable levels. Meanwhile, this study found that the dietary intake of OPEs through food is relatively low, but twice as high as other studies, requiring serious attention. The research findings suggest that the human risk assessment indicates potential adverse effects on human health due to OPEs in the soil–plant system along the coast of South China. This study provides a crucial foundation for managing safety risks in agricultural operations involving OPEs. [ABSTRACT FROM AUTHOR]

The occurrence, distribution, and ecological risk assessment of 36 antibiotics from five groups, including macrolides (MLs), fluoroquinolones (FQs), tetracyclines (TCs), amphenicols (APs), and sulfonamides (SAs), were investigated for the first time in the Anning River, Sichuan Province, China. The results show that antibiotics were widely present in the sediments of the Anning River, with a total of 22 antibiotics detected. FQs were among the most abundant antibiotics, followed by TCs, MLs, APs, and SAs. The total concentrations of antibiotics in surface sediments varied from 0.05 to 53.35 ng/g, with an average of 8.09 ng/g. Among these groups, MLs, FQs, and TCs emerged as the predominant classes of antibiotics. The midstream sediments showed the highest residual levels of antibiotics, with lower levels observed in the downstream and upstream sediments. Anthropogenic activities, such as human clinical practices and animal breeding, might be sources of antibiotics released into the river. An ecological risk assessment revealed that trimethoprim from the SA group exhibited high risks, and MLs showed medium risks in the Anning River, whereas most antibiotics presented minimal to low risks. This study provides valuable information on antibiotic pollution in the upstream region of the Yangtze River, and future management measures are needed for the Anning River. [ABSTRACT FROM AUTHOR]

Sociability indicates the variances of affinity and solitary among animals and it is strongly correlated with cortisol levels. This study was conducted in 2020, from September 16th to October 15th, at the Zhuanglang Musk Deer Farm in Gansu Province of China. We recorded behaviours of 41 captive Alpine musk deer (Moschus chrysogaster) (in 12 enclosures) using the integrated methods of focal sampling and all occurrence recording for sociability analysis, while non-invasive sampling methods and radioimmunoassay were used to collect and measure faecal cortisol level. The relationship between the sociability of captive Alpine musk deer and faecal cortisol hormone was analysed. The results showed that the sociability of captive Alpine musk deer was 14.754% (± 3.026%) (n=41). Individuals in high-density enclosures (19.090% ± 4.497%, n=26) were significantly more sociable as compared to those in low-density enclosures (7.979% ± 2.640%, n=15; P=0.011). The cortisol level of Alpine musk deer was 109.215 (± 5.349) ng/g (n=41). The cortisol level of female individuals (120.419 ± 11.103 ng/g, n=14) was significantly higher than that of male individuals (103.406 ± 5.575 ng/g, n=27; P=0.008). The male musk deer in high sociability (44.114% ± 9.364%, n=8) had lower faecal cortisol levels (102.415 ± 14.885 ng/g, n=8) than those in low sociability (5.518% ± 1.369%, n=19) (103.823 ± 5.243 ng/g, n=19), however these differences were not significant (P=0.911). The female musk deer in high sociability (20.556% ± 2.174%, n=3) had significantly lower (P=0.035) faecal cortisol levels (77.018 ± 17.036 ng/g, n=3) than those in low sociability (7.773% ± 1.595%, n=11) (132.256 ± 11.079 ng/g, n=11), which could be related to maternal care and weaning period. It is suggested that the enclosing density should be increased to improve captive Alpine musk deer’s (especially female musk deer) sociability in the domestication of musk deer. [ABSTRACT FROM AUTHOR]

A sedimentary record of the 19 organochlorine pesticides (OCPs) pollutants from Dongping Lake, north China, is presented in this study. According to the dating of core sediment and OCP content analysis in samples, from 1904 to 2016, the total concentration of OCPs varied from undetectable levels (n.d.) to 33.1 ng/g. The OCP concentration was first detected in the samples of 1938, and then gradually increased to a peak level in 2000 thereafter decreased until 2016. Among the detected OCPs, hexachlorocyclohexanes (HCHs) and dichlorodiphenyltrichloroethanes (DDTs) were the predominant and the most frequently detected contaminants in the core sediment, with concentrations ranging from n.d. to 16.9 ng/g and from n.d. to 8.8 ng/g, respectively. The distribution of OCPs in the sediments was affected by organic carbon concentration, showing a significant positive correlation (r = 0.93, p < 0.001), especially for HCHs (r = 0.98, p < 0.001). The source analysis showed that HCH contamination mainly derived from historical use of technical HCHs, while in recent years, it derived from lindane usage. DDT pollution was attributed to historical use of technical DDTs, as well as the microbial degradation of historic DDT residues. Finally, risk analysis was performed for OCPs in sediment cores based on sediment quality guidelines from the Canadian Council of Ministers of the Environment, showing that DDTs presented a high ecological toxicity risk during the period of 1959–2010. [ABSTRACT FROM AUTHOR]

Hexabromocyclododecane (HBCD) is the most important flame retardant that has been used in Expanded Polystyrene foam and Extruded Polystyrene foam in the past forty years across the world. China was the major producer and user of HBCD, and the total HBCD production was about 0.3 million tons. Although HBCD was completely banned in China in 2021 because of its long-range transport, bioaccumulation and toxicity, there is still a lot of residue in the environment. Therefore, we reviewed multiple studies concerning the distribution of HBCD in diverse environmental matrices, such as in the air, dust, soil, water, sediment, and biota. Results revealed that HBCD levels in different environments in China present geographical variation and were at a high level compared with other countries. In all environmental media, relatively high HBCD concentrations have been found in industrial and urban areas. Industrialization and urbanization are two important factors that influence the concentration and distribution of HBCD in the environment. In terms of isomer, γ-HBCD was the dominant isomer in soil, water, and sediment, while in the biota α-HBCD was the predominant isomer. [ABSTRACT FROM AUTHOR]

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Gypsum is a widespread mineral in various sedimentary deposits. It precipitates from natural aqueous systems with trace amounts of U but almost no Th, rendering it a potentially valuable U–Th geochronometer. However, no gypsum RM for U–Th dating has been available. In this work, two natural gypsum reference materials (PXCG-1, PXCG-2) from the PiXiao cave, southwest China were prepared and characterized for U–Th dating. U–Th contents and isotope ratios were measured on a multi-collector inductively coupled plasma mass spectrometer (MC-ICP-MS) using the isotope dilution technique. Data from three different laboratories show good agreement in 238U content, δ234U (234U/238U relative to secular equilibrium value), 230Th/238U activity ratio, and 230Th ages (corrected) (corrected by assuming the initial 230Th/232Th ratio of the average crust value). The recommended values with the uncertainties (2σ) of these two gypsum RMs, 238U content = 1844 ± 39 ng g−1, δ234U = 229.3 ± 3.9‰, 230Th/238Uactivity = 0.5741 ± 0.0036, 230Th ages (corrected) = 66.97 ± 0.31 ka BP for PXCG-1, and 238U content = 1636 ± 50 ng g−1, δ234U = 61.0 ± 2.4‰, 230Th/238Uactivity = 0.9797 ± 0.0034, 230Th ages (corrected) = 260.82 ± 3.39 ka BP for PXCG-2, respectively. Information values of 232Th content, 230Th/232Th atomic ratio, 230Th age (uncorrected), and δ234Uinitial are also provided. PXCG-1 and PXCG-2 are the first reported gypsum age RMs for U–Th dating, making them a useful complement to the widely distributed carbonate age reference materials for U–Th disequilibrium dating in Pleistocene–Holocene deposits. [ABSTRACT FROM AUTHOR]

The presence of endocrine-disrupting chemicals (EDCs) in aquatic environments such as water, sediment, and sludge received more and more attention. However, the bioaccumulate properties of EDCs, particularly progestins and androgens, in various tissues of different wild freshwater fish species, as well as their effects on human health, have not been fully studied. The muscle, liver, and gills of three wild fish species obtained from the East Dongting Lake in southern China were examined for the presence of 19 EDCs (4 progestins, 5 androgens, 6 estrogens, and 4 phenols). Seventeen analytes were detected in all fish samples, and the concentrations of progestins, androgens, estrogens, and phenols ranged from ND–78.80 ng/g (wet weight, ww), ND–50.40 ng/g ww, ND–3573.82 ng/g ww, and ND–88.17 ng/g ww, respectively. The bioaccumulation of some EDCs in wild fish from East Dongting Lake was species-specific. Additionally, AND, EES, P4, and E2 were discovered in the liver at higher levels than in the muscle, suggesting that livers had a larger ability for enriching these EDCs than the muscle. Furthermore, the relationships between the fish sizes and the EDC concentrations indicated that total weight and length had a negligible impact on the bioaccumulation of EDCs in various fish species. Most importantly, the effects of EDCs on human health as a result of fish consumption were assessed. Although the estimated daily intakes (EDIs) of most EDCs were much lower compared with the corresponding acceptable daily intakes (ADIs) via consuming fish collected in this study, the EDI of EE2 in Silurus asotus was higher than the ADI of E2, indicating that Silurus asotus from East Dongting Lake should be eaten in moderation by local residents. [ABSTRACT FROM AUTHOR]

Bisphenol A (BPA) is mainly used to produce polycarbonate consumer products. However, the occurrence of BPA and other bisphenol analogues (BPs) in polystyrene-made plastic products, such as white foam take-out containers (WFTOCs), has not been well investigated. In this study, occurrence of 20 BPs in WFTOC samples collected from China, Canada, and Poland were investigated with a sample size of 152. Results showed that 11 out of 20 BPs have been detected at least in one WFTOC sample. Among them, BPA was the most frequently detected BP, followed by bisphenol S (BPS) and bisphenol AF, while BPF was the least detected BP. Very high concentrations of BPA and BPS were detected in WFTOCs from China (mean 2694 and 552 ng/g), compared with Canada (81 and 45 ng/g, respectively) and Poland (95 and 16 ng/g). Other BPs, such as bisphenol TMC (BPTMC; detection frequency 65%, range < LOQ − 224 ng/g), bisphenol G (17%, < LOQ − 11 ng/g), and bisphenol BP (11%, < LOQ − 1.6 ng/g), were also detected in Chinese WFTOC samples. The mean partitioning coefficients of BPA, BPS, bisphenol AP, and BPTMC between WFTOCs and tap water, 10% ethanol, 50% ethanol, corn oil, or steamed rice were 0.22 − 2.9%, 0.16 − 5.1%, 0.11 − 7.5%, 2.3 − 6.5%, or 0.19 − 0.36%, respectively. The estimated daily intake of BPA, BPS, and BPTMC through using WFTOCs were 0.50 − 547, 0.054 − 229, and < 0.66 ng/kg bw/day, respectively, for general population in China, Canada, and Poland. Overall, this study first reveals the unexpected presence of BPs in WFTOCs made of polystyrene, which contributes to the better understanding of the sources of human exposure to BPs. [ABSTRACT FROM AUTHOR]

Organophosphate esters (OPEs) are emerging pollutants. Currently, research on OPEs in tree rings is still limited. In this study, tree rings of five arbor species from Sichuan Province, China, were sampled to study the occurrence and distribution of six OPEs, which were quantitatively analyzed by gas chromatography–mass spectrometry (GC–MS). The total concentrations of OPEs in all samples ranged from 189.79 (Fir species) to 341.23 ng/g (Toona sinensis), with average concentration of 284.77 ± 46.66 ng/g. So, arbor could be used as good passive samplers for OPEs. The levels of OPEs among five arbor species showed no significant difference (p = 0.668 > 0.05), suggesting that the pollution status of OPEs in a region or country could be roughly assessed by any arbor tree species. In this study area, tris(2-butoxyethyl) phosphate (TBEP) was the dominant OPEs followed by tri(2-chloroethyl) phosphate (TCEP). Tris(2-ethylhexyl) phosphate (TEHP) and tri-n-butyl phosphate (TnBP) showed relatively stable concentrations in each arbor species, while the other four OPEs including TBEP, triphenyl phosphate (TPhP), tri(chloropropyl) phosphate (TCPP) and TCEP had significantly different concentrations. Interestingly, the absorption and accumulation of OPEs by tree rings of arbor species were quite different from that of inorganic elements reported by other studies. [ABSTRACT FROM AUTHOR]

Due to their significant environmental impact, there has been a gradual restriction of the production and utilization of legacy per- and polyfluoroalkyl substances (PFAS), leading to continuous development and adoption of novel alternatives. To effectively identify the potential environmental risks from crop consumption, the levels of 25 PFAS, including fourteen perfluoroalkyl acids (PFAAs), two precursor substances and nine novel alternatives, in agricultural soils and edible parts of various crops around a fluoride industrial park (FIP) in Changshu city, China, were measured. The concentration of ΣPFAS in the edible parts of all crops ranged from 11.64 to 299.5 ng/g, with perfluorobutanoic acid (PFBA) being the dominant compound, accounting for an average of 71% of ΣPFAS. The precursor substance, N-methylperfluoro-octanesulfonamidoacetic acid (N-MeFOSAA), was detected in all crop samples. Different types of crops showed distinguishing accumulation profiles for the PFAS. Solanaceae and leafy vegetables showed higher levels of PFAS contamination, with the highest ΣPFAS concentrations reaching 190.91 and 175.29 ng/g, respectively. The highest ΣAlternative was detected in leafy vegetables at 15.21 ng/g. The levels of human exposure to PFAS through crop consumption for various aged groups were also evaluated. The maximum exposure to PFOA for urban toddlers reached 109.8% of the standard value set by the European Food Safety Authority (EFSA). In addition, short-chained PFAAs and novel alternatives may pose potential risks to human health via crop consumption. [ABSTRACT FROM AUTHOR]

To study the influence of dredged sediment transportation on the distribution of short-chain chlorinated paraffins (SCCPs, C10-13), medium-chain chlorinated paraffins (MCCPs, C13-17), and long-chain chlorinated paraffins (LCCPs, C18-28), 62 surficial sediment samples were collected from the Huangpu River and the Shanghai offshore areas, East China. A high-performance liquid chromatograph coupled with a quadrupole time-of-flight mass spectrometry system (HPLC-QTOF MS) was employed to measure CPs. The concentrations of CPs in sediment samples ranged from 8.76 to 1270.7 ng g−1 for SCCPs, from 22.03 to 1730.78 ng g−1 for MCCPs, and from undetected (ND) to 236.86 ng g−1 for LCCPs. The concentrations were lower than those that can be toxic to organisms. Furthermore, the influence of sediment dredging activity on the distribution of CPs was also investigated. The concentrations of CPs in sediment discarding areas were significantly higher than those in the surrounding areas, but this result is consistent with the concentrations in the Huangpu River sediments where CPs originated. Also, the SCCP congener group in the discarding area was similar to that in the Huangpu River. These findings indicated that CPs exhibited lower migration in the discarding area and had limited environmental impacts. [ABSTRACT FROM AUTHOR]

Dietary consumption of contaminated vegetables is the main route of human exposure to polycyclic aromatic hydrocarbons (PAHs). However, there is a lack of research on PAHs in vegetables from northwest China. In this study, the concentrations, sources, and risk assessment of PAHs in the soil and vegetables of Urumqi, an urbanized city in Xinjiang, China, were investigated. The total concentrations of 16 PAHs in soil and vegetable samples ranged 10.58–77.20 and 93.7–1071.8 ng/g, with average values of 2.86 and 242.76 ng/g, respectively. Among vegetable samples, the concentrations were in the order: leafy vegetables (299.08 ng/g) > fruits (192.65 ng/g) > vegetable roots (152.05 ng/g). The source apportionment of PAHs was identified using positive matrix factorization. The primary sources of PAHs in soil samples are oil spills, traffic emissions, coal combustion, and coke combustion. The main sources of PAHs in vegetable samples are oil spills and burning of grass, wood, coal, and coke. In soil samples, the ecological risk caused by PAHs is at a safe level, and the incremental lifetime cancer risks (ILCRs) of ingestion exposure exceed 1.0 × 10–6, which will pose potential risks to human body. The ILCRs of vegetable samples revealed that all groups had potential risks from onion and cabbage consumption (ILCRs > 1.0 × 10–6). In particular, adult women had a higher risk of cancer (ILCRs > 1.0 × 10–4). These results emphasize the importance of combating PAHs pollution in vegetable bases. [ABSTRACT FROM AUTHOR]

Tidal flat areas are important resources for land development and are becoming antibiotic resistance receivers that trigger major health concerns. The spatial distributions of forty-nine antibiotics, nine antibiotic resistance genes (ARGs), one mobile gene element (MGE) gene, and nine available metals in the soils and sediments along the coastlines of the Yellow Sea in China were quantified. Hierarchical linear model analysis was used to explore relationships between the antibiotics and ARGs across multiple effects resulting from human activities and environmental factors. Fish farm sediments and farmland soils showed high levels of quinolones (QNs) (maximum 637 ng·g−1), sulfonamides (SAs) (maximum 221 ng·g−1), and corresponding ARGs. Significant positive correlations (P from 5.47 × 10−14 to 0.0487) were observed between the antibiotics (QNs, SAs, and chlortetracycline) and their corresponding ARGs (qnrA, qnrD, aac(6')-Ib-cr, dfrA, sul2, and tetA), indicating the selective pressure from antibiotics in soils and sediments. Nine available metals had positive correlations with at least one ARG, indicating heavy metal pollution could enhance the ARGs. Sheep and poultry husbandry and marine aquaculture contribute the most to the antibiotic resistance in the coastlines. In conclusion, antibiotic pollutions have promoting effects at sub-inhibitory concentrations and more attention should be given to inhibit the enrichment of ARGs during tidal flat reclamation processes. The study also suggests the induction effects from metal pollutions, MGE spread, and the antibiotic pollutions from the usage in livestock and aquaculture. [ABSTRACT FROM AUTHOR]

Contamination by hexabromocyclododecanes (HBCDDs) in the soil environment is an ongoing concern because of their "specific exemption" on the production and use in China. In this study, spatial distribution, temporal trend, and diastereoisomer profiles of HBCDDs were examined in surface soils collected in Jinan, China. Concentrations of ΣHBCDD (sum of α-, β-, and γ-HBCDDs) in soils ranged from 1.70 to 228 ng/g dry weight (dw), with a mean value of 26.1 ng/g dw. Soils collected from e-waste dismantling sites (mean 146 ng/g dw) contained significantly higher concentrations of ΣHBCDD than those of urban (15.5 ng/g dw) and farmland soils (3.86 ng/g dw) (p < 0.01). The temporal trend suggested that ΣHBCDD levels in the industrial area rose significantly between 2014 and 2019 (p < 0.05), with an annual increase of 12%. An increase in ΣHBCDD levels was also observed in urban and farmland soil samples during the study period, although it did not reach a significant level (p > 0.05). All surface soils were dominated by γ-HBCDD (mean 60.7% of total concentrations); however, the proportions of α-isomer increased from 28.7% in urban and rural soils to 43.4% in industrial soils. The calculated risk quotients of HBCDDs present in soils were at least 25-fold lower than the threshold limit value. The mean mass inventory of HBCDDs was approximately 2501 kg in the cultivated land of Jinan City; further studies are needed to discern the uptake of HBCDDs by crops and the fate of these chemicals in agricultural ecosystems. [ABSTRACT FROM AUTHOR]

The transformation products of triclosan (5-chloro-2-(2,4-dichlorophenoxy)phenol) may be more persistent and toxic than their parent compound, yet their occurrence in aquatic environments is poorly understood. In this study, we identified three transformation products in sediment samples from Taihu Lake and compared their concentrations with the parent compound triclosan. Triclosan in Taihu Lake was at low level, ranging from 0.086 to 1.1 ng/L in surface water and 0.0058–8.3 ng/g in sediments. The three detected transformation products included methyl triclosan, chlorinated triclosan derivatives, and methyl chlorinated triclosan derivatives. Those transformation products constituted 0.73–87.5% of the total triclosan (total triclosan is the sum of triclosan, methyl triclosan, chlorinated triclosan derivatives, and methyl chlorinated triclosan derivatives on a molar basis), indicating that the ecological risk of transformation products should be considered in addition to the parent compound. Different transformation products had distinct spatial distributions. Chlorinated triclosan derivatives had the highest concentration in samples from the northwest region (0.016–0.21 ng/g) of the lake and were positively correlated with triclosan, which may indicate the possible transformation from triclosan to chlorinated triclosan derivatives. Methyl triclosan and methyl chlorinated triclosan derivatives were generally higher in samples from the center of the lake (0.22–0.28 ng/g for methyl triclosan and 0.017–0.021 ng/g for methyl chlorinated triclosan derivatives, respectively), indicating the possible occurrence of in situ microbial methylation of triclosan and chlorinated triclosan derivatives and the accumulation of those methylated analogues in Taihu Lake. [ABSTRACT FROM AUTHOR]

To assess the impacts of e-waste regulations on environmental pollution, the levels, compositions, and human exposure assessment of organophosphorus flame retardants (PFRs), emerging PFRs (ePFRs), phthalate esters (PAEs), and alternative plasticizers (APs) were investigated in indoor dust samples collected from homes in a former e-waste dismantling area in 2013 and in 2017, 4 years after the implementation of legislation and regulations governing e-waste dismantling activities in this area. The median concentrations of ΣPFRs, ΣePFRs, ΣPAEs, and ΣAPs in dust decreased from 5680, 1650, 167,200, and 140,600 ng/g in 2013 to 1210, 476, 95,000, and 45,300 ng/g in 2017, respectively, suggesting that the national and local regulations prohibiting primitive e-waste dismantling activities is effective in mitigating the pollution status for these chemicals. In the analyzed dust samples, tris(1-chloro-2-propyl) phosphate (TCIPP), triphenyl phosphate (TPHP), resorcinol bis(diphenylphosphate) (RDP), and bisphenol A-bis(diphenyl phosphate) (BDP) were the major PFRs/ePFRs, contributing to 77% and 76% of the total PFRs/ePFRs in 2013 and 2017, respectively. Di(2-ethylhexyl) phthalate (DEHP), di-iso-nonyl phthalate (DINP), di-iso-decyl phthalate (DIDP), and di-n-butyl phthalate (DNBP) were the major PAEs/APs, with contributions of 89% and 95% for the total PAEs/APs in 2013 and 2017, respectively. The results of the human exposure assessment demonstrated that exposure to these levels of the target chemicals via dust ingestion and dermal contact was unlikely to cause health concerns for local residents. [ABSTRACT FROM AUTHOR]

Health risks from exposure to contaminants are generally estimated by evaluating concentrations of the contaminants in environmental matrixes. However, accurate health risk assessment is difficult because of uncertainties regarding exposures. This study aims to utilize data on the concentrations of organophosphate flame retardants (OPFRs) in surface soil across China coupled with Monte Carlo simulations to compensate for uncertainties in exposure to evaluate the health risks associated with contamination of soil with this class of flame retardants. Results revealed that concentrations of ∑OPFRs were 0.793-406 ng/g dry weight (dw) with an average of 23.2 ng/g dw. In terms of spatial distribution, higher OPFRs concentrations were found in economically developed regions. Although the values of health risk of OPFRs in soil across China were below the threshold, the high concentrations of OPFRs in soil in some regions should attract more attentions in future. Sensitivity analysis revealed that concentrations of OPFRs in soil, skin adherence factor, and exposure duration were the most sensitive parameters in health risk assessment. In summary, the study indicated that the national scale soil measurement could provide unique information on OPFRs exposure and health risk assessment, which was useful for the management of soil in China and for better understanding of the environmental fate of OPFRs in the global perspective. [ABSTRACT FROM AUTHOR]

As a carrier of toxic substances, household dust has a great impact on human health. Here we collected 73 household dust samples from 27 provinces and 1 municipality in China to investigate the levels, spatial distribution, sources, and carcinogenic risk of 16 polycyclic aromatic hydrocarbons (PAHs). The total concentrations of 14 detected PAHs (∑14 PAHs) ranged from 3.72 to 60,885 ng g−1. High ∑14 PAHs were found in Northeast and Southwest China. High molecular weights (HMW) PAHs (4–6 rings) were predominant PAHs in most dust samples, accounting for 93.6% of ∑14 PAHs. Household fuel, cooking frequency, air conditioning, and smoking were the main factors influencing PAH concentrations in household dust. Principal component analysis model indicated that fossil combustion (81.5%) and biomass combustion and vehicle exhaust (8.1%) are the primary sources of PAHs. Positive matrix factorization model suggested that household cooking and heating contributed about 70% of ∑14 PAHs, and smoking contributed another 30%. The values of benzo[a]pyrene equivalent in rural dust were found to be higher than those in urban dust. The sum of toxic equivalents (TEQs) of 14 PAHs were in range of 0.372–7241 ng g−1, in which 7 HMW PAHs accounted for 98.0 ± 1.98% of the total TEQs. Monte Carlo Simulation showed a low to moderate potential carcinogenic risk of PAHs in household dusts. This study documents comprehensive information on human exposure to PAHs in household dust at a national-scale. [ABSTRACT FROM AUTHOR]

Although the ecological risk of emerging contaminants is currently a research hotspot in China and abroad, few studies have investigated the ecological risk of pesticide pollutants in Chinese coastal sediments. In this study, nine pesticide pollutants included in the "List of New Key Pollutants for Control (2023 Edition)" issued by the Chinese government were used as the research objects, and the environmental exposure of pesticide pollutants in China's coastal sediments was analyzed. The baseline sediment quality criteria were deduced using the balanced distribution method, and a multi-level ecological risk assessment of pesticides in sediment was performed. The results showed that the nine pesticide pollutants were widespread in Chinese coastal sediments, with concentrations ranging from 0.01 ng·g−1 to 330 ng·g−1. The risk quotient assessment showed that endosulfan and DDT posed medium environmental risks to the Chinese coastal sediment environment, and PCBs posed medium risks in some bays of the East China Sea. The semi-probabilistic, optimized semi-probability evaluation and joint probability curve (JPC) assessments all show that endosulfan and DDT pose a certain degree of risk to the environment. [ABSTRACT FROM AUTHOR]

To investigate the effect of pesticide use on surface water, the concentration and distribution characteristics of 57 pesticides and 3 degradation products were analyzed in the farmland soil and surface water in the Xingkai Lake area, including water from paddy fields, drainages and the Xingkai Lake, in Heilongjiang Province, China. Forty-three pesticides and three degradation products were detected in farmland soil. In dry field (corn and soybean field) soil, the main detected pesticides were atrazine and acetochlor with mean concentrations of 26.09 ng·g−1 and 49.08 ng·g−1, respectively. In paddy field soil, oxadiazon, mefenacet and chlorpyrifos were the main detected pesticides with mean concentrations of 14.32 ng·g−1, 78.60 ng·g−1 and 20.03 ng·g−1, respectively. In the surrounding water, including water from paddy fields, drainages and Xingkai Lake, the total concentrations of contaminants detected in the water samples ranged from 71.19 ng·L−1 to 10,145.76 ng·L−1. Of the three sampling periods, the mean concentration of contaminants in the water exhibited its peak during the vegetative period. In the analysis of the drainage water, the primary pesticides detected were atrazine, acetochlor and buprofezin with mean concentrations of 354.83 ng·L−1, 109.09 ng·L−1 and 254.56 ng·L−1, respectively. Atrazine, simetryn, buprofezin and isoprothiolane were the main pesticides detected in Xingkai Lake water, with the mean concentrations of 222.35 ng·L−1, 112.76 ng·L−1, 301.87 ng·L−1 and 138.02 ng·L−1, respectively. The concentrations of contaminants could be correlated with drainage, Da Xingkai Lake and Xiao Xingkai Lake water (ρ > 0.8) suggested that the source of these contaminants in drainage and Xingkai Lake water could be the same. The maximum potentially affected fraction (PAF) values of atrazine, chlorpyrifos and prometryn were higher than 5% in Xingkai Lake water, resulting in high ecological risks. [ABSTRACT FROM AUTHOR]

The extensive use of the parabens triclosan (TCS) and bisphenol A (BPA) has potential adverse effects on human health and aquatic organisms. However, their monitoring information in freshwater lakes is still limited. This study simultaneously summarized the concentrations, spatial distribution characteristics, and correlations of four types of parabens, TCS, and BPA in the surface water and sediment of Baiyang Lake. Finally, the potential risks of target pollutants were evaluated from two aspects: human health risks and ecological risks. The average contaminations of target compounds in surface water and sediment—BPA, TCS, and ∑4 parabens—was 33.1, 26.1, 0.7 ng/L and 24.5, 32.5, 2.5 ng/g, respectively. The total concentration of target compounds at the inlet of the upstream Fu River and Baigouyin River is significantly higher than that near Hunan and the outlet. In addition, Spearman's correlation analysis showed a significant positive correlation between compounds. The health hazards of target compounds in surface water were all within safe limits. However, the risk quotient results indicate that in some locations in surface water, TCS poses a high risk to algae and a moderate risk to invertebrates and fish, and appropriate attention should be paid to these areas. [ABSTRACT FROM AUTHOR]

The organochlorine pesticides (OCPs) are with features of persistence, high toxicity, bioaccumulation and adverse impact on ecosystems and human beings. Although OCPs pollutions have been observed in the plateau lakes, comprehensive understandings in the distribution characteristics and human health risks of OCPs in these valuable but fragile ecosystems are limited. We here investigated the distribution, bioaccumulation process and health risks of OCPs in the Jianhu lake, a representative plateau lake in China. The endrin ketone, endrin aldehyde and heptachlor were the most dominant species in surface and columnar sediments. Their total contents ranged between 0 ~ 1.92 × 103 ng·g−1. The distribution of OCPs in sediment cores combined with chronology information indicated that the fast accumulation of OCPs happened during the last decades. Combining the distribution features of OCPs in different sources with mixing model results of carbon isotope (δ13C), farming area was identified as the main source (46%), and the OCPs were transported to lake by inflow-rivers (37%). The enrichment of OCPs in sediments caused considerable bioaccumulation of OCPs in local fish (∑OCPs 0–3199.93 ng·g−1, dw) with the bio-sediment accumulation factor (BSAF) ranging from ND to 9.41. Moreover, growing time was another key factor governing the accumulation in specific species (Carassius auratus and Cyprinus carpio). Eventually, the carcinogenic risk index (CRI) and exposure risk index (ERI) of the endrin category and aldrin exceeded the reference value, indicating relatively high health risks through consumption of fish. Overall, this study systematically illustrated the bioaccumulation process and health risks of OCPs in the typical plateau lake, providing theoretical support for the better protection of this kind of lakes. [ABSTRACT FROM AUTHOR]

In this study, surface soil samples from 14 representative college school yards in Xi'an, the capital city of Shaanxi province, China, were collected and analyzed for 21 organochlorine pesticides (OCPs). The total concentrations were in the ranges of 0.2-67.0 ng/g. HCHs and DDTs were the most dominant compounds among the 21 OCPs, and their concentrations ranged from 0.1-8.5 to 0.1-56.3 ng/g, respectively. Source identification analysis indicated that the residues of HCHs and DDTs were mostly due to historical use of these chemicals or from other source regions. The quality of all the Xi'an college school yard soils except sample XAUAT was classified as low pollution by OCPs according to the National Environmental Quality Standards for Soils of China (GB15618-1995). [ABSTRACT FROM AUTHOR]

Dietary intake is one of the main pathways for residents to become exposed to chlorinated paraffins (CPs). In China, due to the popularization of nutritional and medicinal edible fungi, consumption has increased on a yearly basis. Edible fungi have a variety of active substances and are consumed daily by residents. However, there is limited information on the concentration and source of chlorinated paraffins in edible fungi. In this study, the concentrations of short‐chain chlorinated paraffins (SCCPs) and medium‐chain chlorinated paraffins (MCCPs) in 105 edible fungi samples and 36 culture material samples were detected. The concentration range of SCCPs was 79.8 ng/g dw to 3879.3 ng/g dw, and the MCCPs was ND to 572.3 ng/g dw. Spearman correlation analysis indicated that the sources of SCCPs and MCCPs in edible fungi were similar (r = 0.57, p < 0.01). The preponderant SCCPs and MCCPs congener group profiles were C10Cl7–8 and C14Cl6–8. CPs were detected in culture materials, the concentration range of SCCPs was 320.2 ng/g dw to 4326 ng/g dw, and the MCCPs was 333.4 ng/g dw to 4517.4 ng/g dw. And the preponderant SCCPs and MCCPs homologues in culture materials were C11–12Cl6 and C14Cl6. The linear discriminant analysis results indicated different contamination models of CPs between edible fungi and culture materials. The mean estimated daily intake values of SCCPs and MCCPs were 308.1 ng/kg bw/d and 94.4 ng/kg bw/d, respectively, indicating no potential health risk posed by CP exposure in edible fungi. [ABSTRACT FROM AUTHOR]

Monitoring and evaluating bird exposure to hazardous pollutants in wetlands are receiving considerable attention. In this study, the occurrence of 18 organochlorine pesticides (OCPs) in the muscle of bean geese (Anser fabalis) and common teals (Anas crecca) collected from Honghu Lake Wetland (HLW), Central China was studied. Additionally, an exposure risk assessment model was applied to obtain risk levels of OCPs to these birds through three oral routes (food intake, water drinking and soil ingestion). The results suggested that the most abundant OCPs detected in the muscle of waterbirds were DDTs (7.68–602 ng/g lipid weight), followed by HCHs (1.39–89.8 ng/g lipid weight). A significant difference (p < 0.05) existed between two species, but most of OCPs exhibited no statistically relationship with age or gender (p > 0.05). The compositional patterns of OCPs combined with ratios of certain metabolites to their parent compounds indicated that all OCPs in the HLW were largely from historical usage except heptachlor. The exposure risk assessment revealed that common teals with lighter weight had greater exposure risks than bean geese. Of the OCPs analyzed, DDTs could probably cause harm to target birds studied here. Exposure via food intake was identified to be significant while soil ingestion and water drinking contributed least, but they should still be concerned. [ABSTRACT FROM AUTHOR]

To analyse the distribution characteristics, potential sources and health risks of PAHs in the surface soil of the Guan River Estuary Industrial Area, 30 samples along the Guan River were collected. Sixteen types of PAHs were detected by gas chromatography-mass spectrometry (GC-MS). The results showed that the total content of the 16 PAHs (Σ16PAHs) ranged from 1212.8–12264.5 ng/g, and the arithmetic mean and median were 3504.8 ng/g and 2396.5 ng/g, respectively. The concentrations of 7 carcinogenic PAHs (Σ7carPAHs) ranged from 546.1–5742.3 ng/g, accounting for 34–54% of the Σ16PAHs. The pollution of the PAHs was intermediate compared with that of other industrial areas in China. Fluoranthene, pyrene and benzo[a] pyrene (BaP) are the main monomer PAHs. There was a weak positive correlation between the total organic carbon and the PAHs, and a negative correlation between the PAHs and the pH was found. The characteristic ratio and principal component analysis (PCA) show that the PAHs mainly come from combustion sources, especially the combustion process of coal and coke from industrial areas. The TEQBaP (toxic equivalency quantity relative to BaP) concentrations of 7 types of carcinogenic PAHs accounted for 99% of the Σ16TEQBaP. According to the Canadian soil environmental quality standard, 87% of the sampling site’s PAH pollution values exceeded the safety value, suggesting that there is a potential ecological risk in the Guan River Estuary industrial area. [ABSTRACT FROM AUTHOR]

The frequent and extensive use of insecticides has caused serious aquatic pollution, thus posing a great threat to ecosystems and public health. In this study, three classes of insecticides including 20 organochlorine pesticides (OCPs), 6 organophosphorus pesticides (OPs), and 8 pyrethroids were analyzed in 24 sediments from the Liaohe River basin. The results showed that all sediment samples were contaminated with insecticides, with the total concentrations ranging from 7.3 ng/g dry weight (dw) to 242.8 ng/g dw. Among them, pyrethroids (2.2–102.5 ng/g dw) contributed 55% of the total insecticide concentration, followed by OCPs (1.3–94.8 ng/g dw) and OPs (2.6–45.5 ng/g dw), representing 24% and 21% of the total concentrations, respectively. For OCPs, hexachlorocyclohexanes (HCHs) and dichlorodiphenyltrichloroethanes (DDTs) showed the highest concentrations of 0.37–37.5 ng/g dw and 0.05–23.2 ng/g dw, respectively. Historical inputs of lindane and technical DDT were the major sources of HCHs and DDTs, respectively, as indicated by isomer or metabolite ratios. Additionally, dichlorvos (0.26–17.1 ng/g dw) was the main OP, while cypermethrin dominated the pyrethroids with the concentrations of 1.6–32.6 ng/g dw. The spatial distribution revealed that significantly higher residues of insecticides were observed in sediments from the Daliao River system than those from the Liao River. This implied that these insecticides were most likely from the discharge of highly polluted sewage and industrial wastewater from adjacent industrial and populous cities as well as urban applications (e.g., landscape maintenance and household pest control). An ecological risk assessment based on risk quotients suggested that the three classes of insecticides analyzed here pose a low risk to aquatic organisms in the study area. [ABSTRACT FROM AUTHOR]

Twenty-nine surface sediments from Chaohu Lake in China and from its six main tributaries were sampled to investigate the concentrations of two important polycyclic musks (PCMs), 1,3,4,6,7,8-hexahydro-4,6,6,7,8,8-hexamethylcyclopenta(g)-2-benzopyran (galaxolide, HHCB) and 7-acetyl-1,1,3,4,4,6-hexamethyl-1,2,3,4-tetrahydronaphthalene (tonalide, AHTN), as well as the concentration of 4,6,7,8-hexahydro-4,6,6,7,8,8-hexamethylcyclopenta(g)-2-benzopyran-1-one (galaxolidon, HHCB-lactone), which is the main degradation product of HHCB. Except for the high concentrations of AHTN and HHCB measured in the Nanfei River (879 ng/g dw and 5,513 ng/g dw, respectively), the levels of AHTN and HHCB in the river sediments were 7.08–44.9 ng/g dw and 20.6–268 ng/g dw, respectively, which are slightly lower than those documented in various areas worldwide. The concentrations of AHTN and HHCB in the sediments of Chaohu Lake were one or two orders of magnitude lower than those in the tributary rivers and showed a clear regional distribution. The concentrations of HHCB-lactone were comparable to those of HHCB and presented a significant positive correlation with the concentrations of HHCB, suggesting that the HHCB-lactone originated directly from the degradation of HHCB in wastewater treatment plants (WWTPs) or in the natural environment. The diagnostic ratios of HHCB/AHTN and HHCB-lactone/HHCB and the enantiomeric fractions (EFs) of these PCMs showed that the direct origins of the target PCMs in the study area were municipal and industrial wastewaters discharged from adjacent cities or point sources and that the HHCB-lactone in sediment originated from the natural degradation of HHCB in the rivers and the lake. The results of the risk assessment showed that the PCMs in the watershed sediments were unlikely to pose a threat to aquatic species. However, the effluents of industrial and municipal wastewaters that are discharged into the Nanfei River should be investigated in future research. [ABSTRACT FROM AUTHOR]

The concentrations, potential sources, and ecological risk of fifteen organochlorine pesticides (OCPs) in urban stream sediments of a Chinese national demonstration eco-industrial park, the Suzhou Industrial Park (SIP), were investigated. ∑OCPs in the sediments were 1.0– 23 ng g−1 (mean = 9.9 ± 5.0 ng g−1). Generally, HCHs and DDTs were the predominant OCPs and contributed 81% of ∑OCPs. Influenced by the difference in hydrological conditions and OCP use history, levels of OCPs in the sediments of the central area of SIP were lower than those of the outer region. Based on the source analysis, HCHs in the sediments were primarily influenced by the historical usage of technical HCH, and DDTs in the sediments were largely influenced by decayed technical DDT and dicofol. Endosulfans and chlordanes in the sediments were largely influenced by weathered sources. Ecological risk analysis suggested OCPs in sediments of most sampling sites would lead to a moderate toxic effect on sediment-dwelling organisms. [ABSTRACT FROM AUTHOR]

Background: Gallstone disease poses a global threat to human health and is strongly linked to environmental factors. However, there is currently no data on the presence of rare earth elements (REEs) in human gallstones. This paper investigates the concentration and distribution of REEs in gallstones for the first time, aiming to explore the environmental implications on human health. Methods: A total of 25 gallstone samples were collected in Shanghai and the content of REEs was measured by Inductively coupled plasma-Mass Spectrometry (ICP-MS) to explore the distribution of REEs in gallstones. Results: The concentration of REEs in gallstones ranged from 4.89 to 190.8 ng/g (mean 39.21). In most of the gallstone analyses, REEs have been detected and generally attributed to environmental exposure or food contamination. The Y/Ho ratio of gallstones was lower than that of continental rocks, similar to that in the blood, indicating limited fractionation during fluid transport processes in the gallbladder. Conclusions: The upper continental crust (UCC)-normalized REEs pattern in gallstones showed depletion of light REEs, while most showed enrichment of heavy REEs. Positive Gd anomalies were found in most samples, while few samples suggested anthropogenic influence. Whether exogenous inputs or in vivo biofractionation lead to changes in REEs fractionated patterns require further analyses. [ABSTRACT FROM AUTHOR]

With the popularization and high-intensity utilization of greenhouse cultivation for crops growth, the pollution of greenhouse soils has been of concern. Therefore, a national-scale survey was conducted to investigate the contamination status, sources, influence factors and the risks of polychlorinated biphenyls (PCBs) and hexachlorobutadiene (HCBD) in greenhouse and nearby open-field soils. Contents of PCBs ranged from 10−6). This study provided a full insight on the contamination status and risks of PCBs and HCBD when guiding greenhouse agriculture activities. [ABSTRACT FROM AUTHOR]

Per- and polyfluoroalkyl substances (PFASs) are bioaccumulative and widely distributed persistent organic pollutants (POPs). Understanding the distribution of and ecological risks posed by PFASs is critical, particularly for PFAS emissions and accumulation from a common urban pollution source. The transformation characteristics and ecological risks of PFASs from a typical aging municipal landfill leachate were systematically monitored and assessed over five years in this study. The results showed that the total PFAS concentrations (ΣPFASs) in the rivers were between 26.4 and 464.3 ng/L, whereas in sediment, ΣPFASs ranged from 9.5 to 58.5 ng/g (w/w). The presence of perfluorooctanoic acid (PFOA) was the most prominent PFAS in both water (39.4–152.3 ng/L) and sediment (1.1–56.1 ng/g). In a five-year monitoring study, the concentration of PFASs in the aging landfill decreased by 23.3%, with higher mean concentrations observed during summer (307.6 ng/L) compared to winter (250.4 ng/L). As for the pollution distribution, the suspended particulate matter–water partition coefficient (log Kd) of carboxylic acid (PFCAs) and perfluoroalkane sulfonic acids (PFSAs) ranged from 1.53 to 2.65, and from 1.77 to 2.82, respectively. PFSAs and long-chain PFCAs exhibited a greater propensity for sediment association compared to short-chain PFCAs. An ecological risk assessment of four typical PFASs, PFOA, perfluorooctane sulfonate (PFOS), perfluorobutanoic acid (PFBA), and perfluorobutane sulfonic acid (PFBS), utilizing the hazard quotient method revealed that the rivers surrounding the typical aging landfill exhibited a low contamination risk for PFOA, while no ecological risks were associated with the other three FPASs. This study contributes to an enhanced comprehension of the occurrence, distribution, and risk of PFASs in the rivers in rivers and sediment surrounding a typical aging landfill site in China, thereby providing crucial reference information for ensuring water quality safety. [ABSTRACT FROM AUTHOR]

The Yellow River Delta (YRD) is the most complete wetland ecosystem in the warm temperate zone of China and is rich in oil resources. However, with petroleum extraction and the development of the economy, pollution of the YRD has been paid increasing attention, in particular, pollution via polycyclic aromatic hydrocarbons (PAHs), as they have caused great harm to human health and the ecosystem balance. Based on the investigations of a research group in 2009, this study re-collected samples according to the same sampling points and analyzed the concentration, composition, source, ecological risk and health risk of PAHs in 2021. The concentration of ΣPAH16 in the surface soil of YRD in 2009 ranged from 2.6 to 8275.46 ng/g, with an average of 1744.41 ng/g. The concentration of ΣPAH16 in 2021 ranged from 56.25 to 582.56 ng/g, with an average of 149.63 ng/g. Therefore, the pollution situation in the YRD in 2021 was significantly improved compared with 2009. The composition of PAHs in soil in 2009 and 2021 was similar, which was dominated by low-ring PAHs. The evaluation results of the toxicity equivalent factor method showed that there was no potential ecological risk in the soil in 2009 and 2021. The evaluation results of the lifetime cancer risk increment model showed that the incremental lifetime cancer risk models (ILCRs) of soil PAHs in 2009 and 2021 were lower than the safety threshold of 10−6; therefore, there was no carcinogenic risk. The existing management measures for oil wells need to be further promoted to protect the regional ecological environment in the YRD. [ABSTRACT FROM AUTHOR]

Purpose: Organic pollutants' transport, transformation, and biological effectiveness in soils depend mainly on their chemical forms. Therefore, in addition to studying the total content of pollutants, it is essential to understand the forms of organic pollutants in soils. In this study, we measured the speciations of polycyclic aromatic hydrocarbons (PAHs), including desorbing fraction, non-desorbing fraction, and bound residues, in soil samples from the Zhongliangshan karst terrain in Chongqing, southwest China. We also investigated the occurrence of PAHs in soils of the region. Moreover, we used principal component analysis (PCA) to analyze the relationship between soil properties and different speciations of PAHs in soils. The contents of ΣPAH16 ranged from 319.69–1215.64 ng/g, with a mean value of 615.02 ng/g. Desorbing fraction PAHs were significant, accounting for 34–81% of the total PAHs. The ratio of different speciations ordered as soluble > organic solvent extracted > bound residues. 2-3-ring were the major components of the total PAHs content in soils and desorbing fraction. PCA analysis determined that soil organic matter (SOM), total nitrogen (TN), and soil bulk density significantly affected the non-desorbing fraction, and pH and total organic carbon (TOC) had a significant positive correlation with the bound residues. The karst area is a complex and fragile ecosystem. The speciation of PAHs in soils is of great importance for assessing their risk and for remediation. However, most studies have focused on the concentration and distribution of PAHs in karst soils. Therefore, in this paper, we investigated the distribution of PAHs in soils in karst areas by investigating the distribution of different speciations of PAHs in soils. We also investigated the key factors influencing the distribution of different speciations. Materials and methods: Ten sites were selected in Zhongliangshan karst terrain, where 0–20 cm of soil was collected and the concentrations of 16 PAHs were measured. Three speciations of 16 PAHs in soils were extracted by sequential extraction. And the standard methods recommended by the Chinese Society of Soil Science were used to determine the basic soil properties. Result and discussion: In this study, we measured the speciation of PAHs in soil samples from the Zhongliangshan karst terrain in Chongqing, southwest China, including desorbing fraction, non-desorbing fraction, and bound residues. The total content of the 16 PAHs ranged from 319.69 to 1215.64 ng/g, with an average value of 615.02 ng/g. The desorbing fraction was significant, accounting for 34–81% of the total PAHs. The ratio of different speciations is ordered as desorbing fraction > non-desorbing fraction > bound residues. 2–3-ring were the major components of the total PAHs content in soils and each speciation. The PCA results show a significant effect of soil organic matter, TN, and soil bulk density on the non-desorbing fraction. pH and TOC had a relatively significant positive correlation with bound residues. Conclusions: This paper investigated the contamination status of PAHs in surface soils in the karst terrain of southwest China, and the speciation of PAHs. Under the special geological structure background in karst areas, studying the occurrence forms and influencing factors of PAHs pollutants in soils is of great significance for a deeper understanding of the occurrence forms of pollutants and effective control of their diffusion. [ABSTRACT FROM AUTHOR]

Organophosphorus flame retardants (OPFRs) are widely used in various industrial manufacturing processes; thus, their environmental impact in agglomerated industrial areas is of great concern. In this study, seventeen kinds of OPFRs and five kinds of organophosphate diesters (Di-OPs) in water and upper sediment samples from two urban rivers in the agglomerated industrial area of Shenzhen city, China, were investigated. The results showed that the total concentrations of detectable OPFRs ranged from 3438.83 to 12,838.87 ng/L with an average of 6494.94 ng/L in water samples and from 47.16 to 524.46 ng/g (dry weight, dw) with an average of 181.48 ng/g dw in sediment. The values were higher than those in other rivers worldwide. Tris(2-chloroethyl) phosphate (TCEP) is the predominant OPFRs in water and upper sediment, up to 10,664.23 ng/L in water and 414.12 ng/g dw in sediment. The total concentration of OPFRs of sediment samples in the Maozhou River was around twice as high as in the Guanlan River. The results indicated that the level of OPFRs was associated with the industrial activity intensity. Di-OPs exhibited lower concentrations than their parent compounds, and can be attributed to the degradation/metabolism of their parent compounds in the river. The sediment–water partition of OPFRs is significantly correlated with their log Kow values. Risk assessment revealed moderate ecological risks posed by OPFRs in water to aquatic organisms. The present study revealed the pollution status of OPFRs in rivers from agglomerated industrial and residential areas. [ABSTRACT FROM AUTHOR]

Concern over the influences of constant addition of emerging anthropogenic chemicals to the environment has become a public issue during the rapid urbanization. Here, we investigated the occurrence of organophosphate esters (OPEs) in soil and corresponding tree bark in a megacity, Western China. Our results showed levels of OPEs in tree bark (1250 ± 573 ng/g dry weight (dw)) were 1–2 orders of magnitude higher than those in soil (40.4 ± 30.8 ng/g dw). Rooster Mountain is a background mountain area, exhibiting significantly lower concentrations of OPEs in soil and tree bark than those in other sites with relatively high population density. This result highlights the effect of human activities on the distribution of OPEs in environmental matrices. Alkyl-OPEs were predominant compounds in soil, whereas halogenated- (Cl-) OPEs were characterized in tree bark. Furthermore, tris(2-chloroethyl) phosphate (TCEP) positively correlated with tris(2-chloroisopropyl) phosphate (TCIPP) in soil (r2 = 0.43, P < 0.05) while negatively correlated with TCIPP in tree bark (r2 = 0.31, P < 0.05). The ratios of logarithm concentrations of OPEs in tree bark to those in soil correlated well with logKOA values of OPEs from 6 to 10, indicating the equilibrium status was achieved between OPE partitioning in soil and in tree bark. Nevertheless, tris (2-butoxyethyl) phosphate (TBEP) and tris(2-ethylhexyl) phosphate (TEHP) with high values of logKOA deviated from this linear tendency, which was possibly due to the fact that they were subjected to the particle-bound deposition process, leading to partition into the soil. [ABSTRACT FROM AUTHOR]

Novel brominated flame retardants (NBFRs) have been widely used as alternatives to legacy BFRs. However, information on the contamination status and human exposure risks of electronic waste (e-waste)-derived NBFRs in the e-waste workplace is limited. In this study, six NBFRs and the legacy BFRs, hexabromocyclododecanes (HBCDs), were analyzed in 50 dust samples from an e-waste-dismantling workplace in Central China. The dust concentration of NBFRs in e-waste-dismantling workshops (median, 157–169 ng/g) was found to be significantly higher than those in an outdoor environment (17.3 ng/g) (p < 0.01). Differently, the highest median concentration of HBCDs was found in dust from the dismantling workshop for cellphones and computers (367 ng/g) among studied areas. The bis(2-ethylhexyl)-3,4,5,6-tetrabromo-phthalate (BEHTBP) was the predominant compound, which contributed 66.0–88.0% of measured NBFR concentrations. NBFRs might originate from plastic and rubber materials in wastes based on the correlation and principal component analysis. Moreover, the total estimated daily intakes (average scenario) of NBFRs were calculated at 2.64 × 10−2 ng/kg bw/d and 2.91× 10−2 ng/kg bw/d for the male and female dismantling workers, respectively, via dust ingestion, inhalation, and dermal contact pathways, which were lower than the reference dose values, and thus indicated a limited human exposure risk for NBFRs at the current level. Although the dust concentrations and daily intakes of NBFRs were still lower than those of other emerging pollutants (e.g., organophosphate and nitrogenous flame retardants) measured in the same sampling set, the elevated levels of NBFRs suggested the progressive BFR replacement process in China, which deserves more attention regarding their adverse effects on both the environment and human health. [ABSTRACT FROM AUTHOR]

The concentrations of typical organochlorine pesticides (OCPs) (DDTs, HCHs, PCP-Na, and HCB) were measured to understand distribution and source of OCPs in surface and columnar sediments of Poyang Lake in 2006. And OCPS concentrations in surface sediment in 2017 were made a comparison with those in 2006 at several same sampling sites. OCPs showed higher concentrations in main stream than in river mouths (entrance of river flow into lake) of the lake. The average concentrations of HCHs and DDTs were 4.63 ± 3.86 and 20.15 ± 26.86 ng/g in surface sediments in 2006, respectively. Concentrations of OCPs in 2017 were lower than in 2006, such as HCHs average 1.98 ± 2.04 ng/g and DDTs average 4.87 ± 1.48 ng/g in 2017, indicating historical residual and degradation. The primary isomers of HCHs and DDTs in the lake were α-HCH, γ-HCH and p, p′-DDD, respectively. HCHs were from historical residual and lindane application. DDTs were from historical residual. PCP-Na total concentrations in surface sediment were 77.36 ng/g in 2006 and 44.04 ng/g in 2017. The concentration of HCB residues in surface sediment was 0.92 ± 0.90 ng/g in 2006 and 0.42 ± 0.38 ng/g in 2017. The concentrations of OCPs in columnar sediments showed annual variations, and the peak concentrations occurred in 1953, 1961, 1974, 1982, and 1995, showing close relations with onset of production OCPs pesticide in 1950s and its later prohibition in 1980s and a large number agricultural cultivated land decrease in 1990s in China. The concentrations of HCB in columnar sediments were average 2.33 ± 1.26 ng/g. OCPs of columnar sediments were from historical residues and lindane input. The main contamination of OCPs was PCP-Na and p, p′-DDD in Poyang Lake. On the whole, the combination of surface samples (0-5 cm in depth) and columnar samples (0-38 cm in depth) in a single study would give insight into OCPs pollution levels in different years (temporal resolution) and in different regions (spatial resolution) in Poyang Lake. [ABSTRACT FROM AUTHOR]

In this study, the residual status of four chiral pesticides including metalaxyl, napropamide, triticonazole, metconazole, and their enantiomers/stereoisomers were investigated in agricultural soils across China. The levels in the soils were detected as non-detected (n.d.)–16.67 ng/g for metalaxyl with a median of 0.14 ng/g; 0.004–32.99 ng/g for napropamide with a median of 0.29 ng/g; n.d.–207.39 ng/g for triticonazole with a median of 1.29 ng/g; and n.d.–71.83 ng/g for metconazole with a median of 1.03 ng/g, respectively. Enantiomer/stereoisomer-specific residues were observed for metalaxyl and triticonazole. R-Metalaxyl and R-triticonazole were identified as the major enantiomers in the soils for the two pesticides. There was no obvious enantioselective residue for napropamide in most of the soils. As for metconazole, metconazole-1 and metconazole-4 were identified as the major stereoisomers in the soils. These results suggest that enantiomer/stereoisomer-specific risk should be considered when assessing the ecological safety of these pesticides in soils. [ABSTRACT FROM AUTHOR]

Although organochlorine pesticides (OCPs) in the Stockholm Convention List were banned for a period of time, the residue of OCPs in environment was still detected recently. Therefore, the continuous environmental monitoring was necessary and important for the deep understanding on the temporal trend of environmental fate of OCPs. In this study, the national scale surface soil samples in 26 provinces of China in 2012 were collected, and 28 OCPs were analyzed. The mean concentrations (ng/g dw) of Σhexachlorocyclohexanes (HCHs), Σdichlorodiphenyltrichloroethane (DDTs), hexachlorobenzene (HCB), and hexachlorobutadiene (HCBD) were 2.47 ± 5.4, 4.29 ± 8.28, 3.33 ± 7.68, and 0.041 ± 0.097, respectively. The correlations between OCPs concentrations with temperature, latitude, and longitude were conducted for the deep study of the spatial distribution pattern of OCPs. It was found that HCHs, HCB, and HCBD are positively correlated with latitude and longitude; however, the correlations were not significant. HCHs followed the secondary distribution pattern, and DDTs followed both the primary and/or secondary distribution patterns. Except for HCB, other OCPs showed a gradual downward trend from 2005 to 2012, indicating the effectiveness of the phase-out of OCPs. In summary, the results of the study provided new insight into the related studies, which will help us to better understand the long-term environmental fate of OCPs on large scales. [ABSTRACT FROM AUTHOR]

A method of ultra-high performance liquid chromatography-quadrupole / electrostatic field Orbitrap high resolution mass spectrometry was developed for the determination of 16 organophosphate esters (OPEs) in water and sediment samples. The water samples were extracted by solid phase extraction (Oasis HLB column) while the sediment samples were ultrasonically extracted using 0.1% formic acid methanol and then purified using Sep-Pak PSA column. The treated samples were separated on a Hypersil Gold-C18 column (1.9 μmx2.1 mmx50 mm) and eluted with 0.2% aqueous formic acid solution and methanol. The detection and analysis were performed in electrospray ionization and dd-MS2 + confirmation, in positive mode. The analyzed 16 OPEs were quantitated by external standard method. The lowest detection limits were 3.10- 116.70 ng/L and the linear correlation coefficients were 0.940 7-0.999 8. The developed method was used to analyze the target compounds in water samples and sediment samples from Luoma Lake. In 21 water samples, the concentrations of ∑16OPEs were in the range of 2.99-1 113.09 ng/L, with a median concentration of 408.68 ng/L and an average concentration of 420.03 ng/L. In 6 sediment samples, the concentration of ∑16OPEs were in the range of 15.70-41.28 ng/g, with an median concentration of 27.06 ng/g and an average concentrations of 27.49 ng/g. Compared with the data reported from other water bodies in China or other countries, the concentrations of OPEs in Luoma Lake were at a median/low level. Ecological risk assessment showed that triphenyl phosphate (TPhP), tri-o-cresyl phosphate (o-TTP), tri-m-tolyl phosphate (m-TTP) and tri-p-tolyl phosphate (p-TTP) could pose medium or high risks to water and sediments in Luoma Lake at some sites [ABSTRACT FROM AUTHOR]

The present study assessed the residue levels of six parent neonicotinoids (p-NEOs) and four metabolites (m-NEOs) in indoor dust collected from 12 cities of China. Acetamiprid (ACE) and imidacloprid (IMI) were the predominated p-NEOs (detection rates: 98%) with the median values at 4.54 and 7.48 ng/g dry weight (dw), respectively. N-demethyl-acetamiprid (N-dm-ACE) was the most important m-NEO with the median value at 0.69 ng/g dw, while other m-NEOs were rarely detected (detection rates: < 15%). Significant correlation between ACE and thiacloprid (THD) was observed (p < 0.01), indicating their probably concurrent applications. ACE was significantly correlated to N-dm-ACE (p < 0.01), implicating the degradation of ACE in indoor environment. The estimated daily intake (EDIing) of NEOs via dust ingestion were far lower than the acceptable daily intake for NEOs. To our knowledge, this study provided a baseline nationwide investigation on the occurrence of NEOs in indoor dust of China. [ABSTRACT FROM AUTHOR]

A total of 16 polycyclic aromatic hydrocarbons (PAHs) were measured in 28 soil column samples from two contaminated industrial sites in Eastern China. The total concentration of 16 PAHs (∑PAHs) in the surface soil (0–20 cm) was measured up to 52,600 ng/g (dry weight basis) with a remarkable spatial difference in the studied contaminated sites. The concentrations of the ∑PAHs in soils decreased with the increase in soil depth (0–10 m). The surface and subsurface soil presented a tenfold higher concentration than the soil with depth greater than 4 m. Additionally, the vertical migration tendency of the PAHs was found to be correlated significantly with their hydrophobicity (R2 = 0.79, P < 0.01). Naphthalene (with lowest octanol–water partition coefficient among the studied PAHs) showed the greatest average soil depth at which its peak concentration occurred. Furthermore, risk quotient analysis by using benzo[a]pyrene as reference compound showed that 71.4% of the samples exhibited high ecological risk for soil. Moreover, the total carcinogenic risk of the PAHs in the surface soil samples was assessed at 5.61 × 10–5–1.28 × 10–4 and 4.41 × 10–6–9.43 × 10–5 for male and female workers, respectively, in which 67.9%–71.4% of the samples showed potential risk. Generally, these results suggest a further consideration of ecological and health risks associated with PAHs in contaminated sites in Eastern China. [ABSTRACT FROM AUTHOR]

Organochlorine pesticides (OCPs) and polycyclic aromatic hydrocarbons (PAHs) are among the most concerning environmental pollutants due to their highly toxic, persistent and bioaccumulative properties. A total of 111 sediment samples were collected from shallow lakes along the middle-lower reaches of the Yangtze River and the Huaihe River in China for the determination of OCPs and PAHs. OCPs were detected in all of the sediment samples, with residual values ranging from 8.1 ng g−1 dw to 202.9 ng g−1 dw, and the residual values of PAHs ranged from 11.8 ng g−1 dw to 231. 9 ng g−1 dw. Hexachlorocyclohexanes (HCHs) and dichlorodiphenyltrichloroethanes (DDTs) were the major components, accounting for 29.1% ± 18.7% and 21.1% ± 14.3% of the total OCPs and mostly originating from historical use. Similar compositions of PAHs were observed with 3-, 4-, and 5-ringed congeners as the major contributors accounting for 86.0% ± 10.0% of the identified PAHs. Diagnostic ratios of typical PAHs demonstrated mixed sources from petroleum/petrogenic and combustion processes, which were responsible for the PAHs observed in surface sediments from the studied lakes. A sediment risk assessment based on sediment quality guidelines (SQGs) suggested that heptachlor epoxide, p, p′-DDD and lindane could be potential contaminants of greater ecotoxicological concern. [ABSTRACT FROM AUTHOR]

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There have been reports of potential health risks for people from hydrophobic organic pollutants, such as polycyclic aromatic hydrocarbons (PAHs), polychlorinated hydrocarbons (PCHs), and organophosphate flame retardants (OPFRs). When a contaminated site is used for residential housing or public utility and recreation areas, the soil-bound organic pollutants might pose a threat to human health. In this study, we investigated the contamination profiles and potential risks to human health of 15 PAHs, 6 PCHs, and 12 OPFRs in soils from four contaminated sites in China. We used an in vitro method to determine the oral bioaccessibility of soil pollutants. Total PAHs were found at concentrations ranging from 26.4 ng/g to 987 ng/g. PCHs (0.27‒14.3 ng/g) and OPFRs (6.30‒310 ng/g) were detected, but at low levels compared to earlier reports. The levels of PAHs, PCHs, and OPFRs released from contaminated soils into simulated gastrointestinal fluids ranged from 1.74% to 91.0%, 2.51% to 39.6%, and 1.37% to 96.9%, respectively. Based on both spiked and unspiked samples, we found that the oral bioaccessibility of pollutants was correlated with their log K ow and molecular weight, and the total organic carbon content and pH of soils. PAHs in 13 out of 38 contaminated soil samples posed potential high risks to children. When considering oral bioaccessibility, nine soils still posed potential risks, while the risks in the remaining soils became negligible. The contribution of this paper is that it corrects the health risk of soil-bound organic pollutants by detecting bioaccessibility in actual soils from different contaminated sites. [Display omitted] [ABSTRACT FROM AUTHOR]

Patulin (PAT) is a mycotoxin, with several acute, chronic, and cellular level toxic effects, produced by various fungi. A limit for PAT in food of has been set by authorities to guarantee food safety. Research on PAT in tea has been very limited although tea is the second largest beverage in the world. In this paper, HPLC−DAD and GC−MS methods for analysis of PAT in different tea products, such as non-fermented (green tea), partially fermented (oolong tea, white tea, yellow tea), completely fermented (black tea), and post-fermented (dark tea and Pu-erh tea) teas were developed. The methods showed good selectivity with regard to tea pigments and 5-hydroxymethylfurfural (5-HMF) and a recovery of 90–102% for PAT at a 10–100 ppb spiking level. Limit of detection (LOD) and limit of quantification (LOQ) in tea were 1.5 ng/g and 5.0 ng/g for HPLC−UV, and 0.25 ng/g and 0.83 ng/g for GC−MS. HPLC was simpler and more robust, while GC−MS showed higher sensitivity and selectivity. GC−MS was used to validate the HPLC−UV method and prove its accuracy. The PAT content of 219 Chinese tea samples was investigated. Most tea samples contained less than 10 ng/g, ten more than 10 ng/g and two more than 50 ng/g. The results imply that tea products in China are safe with regard to their PAT content. Even an extreme daily consumption of 25 g of the tea with the highest PAT content (124 ng/g), translates to an intake of only 3 μg/person/day, which is still an order of magnitude below the maximum allowed daily intake of 30 µg for an adult. [ABSTRACT FROM AUTHOR]