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Organophosphate esters (OPEs) are emerging pollutants and used extensively in industrial production as alternative to the traditional flame retardants. This study investigated the contamination characteristics and health risks of OPEs in 104 mollusks from 15 cities along the coastal region of South China. Σ8OPEs ranged from 48.2 to 1937 ng/g dw, with a mean value of 295 ng/g dw. TDCIPP, TCPP, and TCEP were the dominant OPEs. Different spatial distributions were observed, with higher concentrations in Guangdong Province. A statistically positive but non-significant linear correlation was found between the trophic level of mollusk and OPEs concentration. The trophic magnification factors were >1, suggesting that OPEs have the potential to biomagnify in mollusks. OPEs in mollusks pose low non-carcinogenic and carcinogenic risks to consumers. This study provides an important basis for managing the safety risks associated with OPEs in mollusks. • Levels of Σ8OPEs in mollusks ranged from 48.2 to 1937 ng/g dw. • Chlorinated phosphate esters (TDCIPP, TCPP, and TCEP) were the dominant OPEs. • OPEs exhibited the potential to biomagnify in mollusks. • OPEs in mollusks posed low non-carcinogenic and carcinogenic risks to consumers. [ABSTRACT FROM AUTHOR]

This study investigates the presence, distribution, and potential impacts of perfluoroalkyl substances (PFASs) and hexabromocyclododecanes (HBCDs) on the Antarctic marine environment. The analysis results from the King Sejong Station, the Jang Bogo Station, and Cape Evans revealed the highest concentrations of both PFASs and HBCDs at King Sejong Station, indicating the significant influence of human activity. Short-chain perfluorocarboxylic acids (PFCAs) dominated the seawater samples, with PFPeA at the highest concentration (0.076 ng/L) at King Sejong Station, whereas perfluorosulfonic acids (PFSAs) were prevalent in the sediments, with PFHxS reaching 0.985 ng/g. Total PFASs in benthos ranged from N.D. to 2.40 ng/g ww across all stations. This indicated the effects of long-range transport and glacial meltwater. α-HBCD was the most common diastereomer in benthos samples, detected in 58.3% of samples, suggesting its selective persistency. Although risk quotient analysis revealed low immediate risks to lower-trophic organisms, potential risks remain owing to their persistence and bioaccumulation potential. Contaminant patterns changed after regulations: perfluorooctanesulfonic acid (PFOS) and perfluorooctanoic acid (PFOA) levels decreased, unregulated PFASs increased, HBCD stereoisomer ratios shifted towards α-HBCD dominance, and overall HBCD concentrations declined. Widespread persistence of regulated substances was observed in Antarctic environments, highlighting the need for comprehensive and long-term monitoring strategies. This study provides essential baseline data on contaminant distributions across the Southern Ocean, contributing to our understanding of emerging pollutants in Antarctic regions and informing future environmental protection efforts. [Display omitted] • Highest PFAS and HBCD levels at King Sejong Station show human activity's impact on Antarctica. • Short-chain PFCAs dominated seawater, indicating long-range transport and glacial melt influence. • α-HBCD predominated in benthos due to bioaccumulation and long-range atmospheric transport. • Risk quotient analysis showed low immediate risk, but long-term ecosystem health concerns persist. [ABSTRACT FROM AUTHOR]

Polycyclic aromatic hydrocarbons (PAHs) are commonly found in the marine environment and can have harmful impacts on marine biodiversity. Therefore, investigation of the occurrence, source and risks of PAHs is of great importance to protect ecosystem and human health. The objectives of this work were to assess the concentrations and distribution of PAHs in marine sediments and in mollusc bivalve (Callista chione) along the Mediterranean coasts of Morocco and finally evaluate the risk to human health caused by exposure to PAHs. Five sediments samples and seventy five C. chione specimens, were collected along the Moroccan Mediterranean coasts. The ∑PAHs levels in sediment varied considerably, varying from 1 to 251 ng/g with an average of 50.38 ng/g, while values for bivalves varied from 1 to 51 ng/g dw with an average concentration of 16.76 ng/g dw. The PAHs profile indicates the dominance of 2 and 3 rings PAHs both in bivalves and sediments. PAH concentrations generally rise as one moves from northeast to northwest part of the studied area, closer to the Strait of Gibraltar. The assessment of PAH isomeric ratios revealed a mixed pyrolytic/petrogenic source. Based on the sediment quality guidelines (SQGs), the risk of PAHs in the sediments was considered to be comparatively low. Similarly, Ecological risk assessment based on risk quotient (RQ) and toxic equivalency factors (TEFs) revealed potentially low ecological risks from PAHs. Exposure to PAHs via bivalve consumption does not cause adverse impacts on the health of consumers following the calculated health risk indices. As the levels of PAHs in biota are not negligible, continuous mentioning marine organisms campaigns should be performed to highlight the distribution and concentration of PAHs and assess the risk for human health from consumption of seafood. [Display omitted] • High concentration of polyaromatic hydrocarbon (PAH) was detected in Fnideq. • Two- and three-ring PAHs were dominant in sediment and bivalves. • The major sources of PAHs are both pyrogenic and petrogenic. • The risk to human health were evaluated at low levels. [ABSTRACT FROM AUTHOR]

This study investigates the presence, distribution, and potential impacts of perfluoroalkyl substances (PFASs) and hexabromocyclododecanes (HBCDs) on the Antarctic marine environment. The analysis results from the King Sejong Station, the Jang Bogo Station, and Cape Evans revealed the highest concentrations of both PFASs and HBCDs at King Sejong Station, indicating the significant influence of human activity. Short-chain perfluorocarboxylic acids (PFCAs) dominated the seawater samples, with PFPeA at the highest concentration (0.076 ng/L) at King Sejong Station, whereas perfluorosulfonic acids (PFSAs) were prevalent in the sediments, with PFHxS reaching 0.985 ng/g. Total PFASs in benthos ranged from N.D. to 2.40 ng/g ww across all stations. This indicated the effects of long-range transport and glacial meltwater. α-HBCD was the most common diastereomer in benthos samples, detected in 58.3% of samples, suggesting its selective persistency. Although risk quotient analysis revealed low immediate risks to lower-trophic organisms, potential risks remain owing to their persistence and bioaccumulation potential. Contaminant patterns changed after regulations: perfluorooctanesulfonic acid (PFOS) and perfluorooctanoic acid (PFOA) levels decreased, unregulated PFASs increased, HBCD stereoisomer ratios shifted towards α-HBCD dominance, and overall HBCD concentrations declined. Widespread persistence of regulated substances was observed in Antarctic environments, highlighting the need for comprehensive and long-term monitoring strategies. This study provides essential baseline data on contaminant distributions across the Southern Ocean, contributing to our understanding of emerging pollutants in Antarctic regions and informing future environmental protection efforts. [Display omitted] • Highest PFAS and HBCD levels at King Sejong Station show human activity's impact on Antarctica. • Short-chain PFCAs dominated seawater, indicating long-range transport and glacial melt influence. • α-HBCD predominated in benthos due to bioaccumulation and long-range atmospheric transport. • Risk quotient analysis showed low immediate risk, but long-term ecosystem health concerns persist. [ABSTRACT FROM AUTHOR]

Polycyclic aromatic hydrocarbons (PAHs) are commonly found in the marine environment and can have harmful impacts on marine biodiversity. Therefore, investigation of the occurrence, source and risks of PAHs is of great importance to protect ecosystem and human health. The objectives of this work were to assess the concentrations and distribution of PAHs in marine sediments and in mollusc bivalve (Callista chione) along the Mediterranean coasts of Morocco and finally evaluate the risk to human health caused by exposure to PAHs. Five sediments samples and seventy five C. chione specimens, were collected along the Moroccan Mediterranean coasts. The ∑PAHs levels in sediment varied considerably, varying from 1 to 251 ng/g with an average of 50.38 ng/g, while values for bivalves varied from 1 to 51 ng/g dw with an average concentration of 16.76 ng/g dw. The PAHs profile indicates the dominance of 2 and 3 rings PAHs both in bivalves and sediments. PAH concentrations generally rise as one moves from northeast to northwest part of the studied area, closer to the Strait of Gibraltar. The assessment of PAH isomeric ratios revealed a mixed pyrolytic/petrogenic source. Based on the sediment quality guidelines (SQGs), the risk of PAHs in the sediments was considered to be comparatively low. Similarly, Ecological risk assessment based on risk quotient (RQ) and toxic equivalency factors (TEFs) revealed potentially low ecological risks from PAHs. Exposure to PAHs via bivalve consumption does not cause adverse impacts on the health of consumers following the calculated health risk indices. As the levels of PAHs in biota are not negligible, continuous mentioning marine organisms campaigns should be performed to highlight the distribution and concentration of PAHs and assess the risk for human health from consumption of seafood. [Display omitted] • High concentration of polyaromatic hydrocarbon (PAH) was detected in Fnideq. • Two- and three-ring PAHs were dominant in sediment and bivalves. • The major sources of PAHs are both pyrogenic and petrogenic. • The risk to human health were evaluated at low levels. [ABSTRACT FROM AUTHOR]

This study investigated the occurrence status, sources, and risk assessment of polycyclic aromatic hydrocarbons (PAHs) in sediments from three typical mangrove areas in Guangxi Province, China. Results showed that the PAH content in the three studied regions ranged from 39.76 ng·g−1 to 164.93 ng·g−1, and the average concentration was 92.87 ng·g−1. The PAHs that were detected were mainly 3-ring and 4-ring. The source of PAHs, as traced by the diagnostic ratio method and principal component analysis, was mainly from combustion. The toxicity risk assessment showed that the content of all PAHs was lower than the Effects Range Low (ERL), and the potential ecological risk was low. The toxicity equivalent (TEQ BaP) content ranged from 4.75 ng·g−1 to 19.20 ng·g−1, with an average of 12.08 ng·g−1. Overall, the ecological risk of PAHs in mangrove sediments in Guangxi is considered low. • 3 and 4-ring PAHs were the main PAHs in sediments from mangrove wetlands in Guangxi province. • PAHs in sediments were mainly derived from coal and oil combustion. • Toxicity and ecological risk levels of PAHs in sediments were low. [ABSTRACT FROM AUTHOR]

The distribution characteristics and risk levels of PAHs in surface sediment in the Honghai Bay of China are studied in this paper. The results showed that the concentration of total PAHs in this area ranged from 100.65 ng·g−1 to 241.31 ng·g−1, with an average concentration of 158.83 ng·g−1. The tricyclic PAHs were the main components in the detected PAHs. PAH pollution levels in this region were low and moderate as compared with adjacent areas. Traceability results showed that the sediment PAHs mainly originate from coal and biomass combustion. PAHs concentrations at some stations were above the Environmental Quality Reference Level. The PAHs toxicity and ecological risk level in surface sediments in the area was determined to be low to moderate by toxicity equivalence testing and risk entropy value assessment. • Tricyclic PAHs were the main PAHs in surface sediment from Honghai Bay, China. • PAHs in Honghai Bay sediments were mainly derived from coal and biomass combustion. • 3 toxicity and ecological risk levels of PAHs in Honghai Bay were low to moderate. [ABSTRACT FROM AUTHOR]

Knowledge about sediment levels and sources of persistent organic pollutants (POPs) in Lanzhou section Yellow River remains limited. Organochlorine pesticides (OCPs) and polychlorinated biphenyls (PCBs) levels in 12 sediment samples from this region were measured by GC/MS. OCPs concentrations ranged from 85.6 to 202 ng/g, while PCBs levels varied between 3.08 and 32.3 ng/g. Our findings demonstrated a significant correlation between these pollutants and total organic matter (TOC), highlighting TOC's role in pollutants distribution. Notably, OCPs and PCBs levels were higher in the eastern section, following the water flow direction. The primary OCPs components were hexachlorocyclohexane (HCH) and dichlorodiphenyltrichloroethane (DDT), whereas PCBs were dominated by perchlorinated compound. Source identification indicated that OCPs primarily originated from historical residues and recent applications, while industrial activities as significant PCBs sources. Sediment quality guidelines and health risk assessments indicated negligible environmental risk. This study providing valuable insights on sediment pollution control and management strategies. [Display omitted] • ΣOCPs and ΣPCBs in eastern YR sediments higher than western • ΣHCHs and ΣDDTs were dominant ΣOCPs; ΣPCBs were dominated by perchlorinated compound. • ΣOCPs from historical inputs; PCBs from waste incineration • The risk posed by ΣPCBs and ΣOCPs in Yellow River sediment was negligible. [ABSTRACT FROM AUTHOR]

Fluorinated liquid-crystal monomers (FLCMs), a new class of potential persistent, bioaccumulative and toxic (PBT) emerging pollutants, are extensively utilized in the display panel of various electronic devices. These compounds have been found in various environmental matrixes and dietary. Our previous studies have documented their ubiquitous occurrence in high fat foodstuffs. Infants, a vulnerable group, are more susceptible to the impacts of these pollutants compared to adults. Herein, we provided an assessment of the health risks posed by FLCMs to infants, focusing on their exposure through infant formula. The presence of FLCMs was detected in all infant formulas, with median concentration of 16.5 ng/g dry weight (dw) and the 95th percentile concentration of 65.7 ng/g dw. The most prevalent pollutant in these formulas was 2-fluoro-4-[4′-propyl-1,1′-bi(cyclohexyl)-4-yl] phenyl trifluoromethyl ether (FPrBP), with median and a 95th percentile concentration of 12.2 ng/g dw and 23.8 ng/g dw, accounting for 55.2% to the total FLCMs. Infants aged 0–6 months had the highest estimated daily intakes (EDIs) of FLCMs, with the EDI median of 267 ng/kg bw/day. FPrBP and 4-[trans-4-(trans-4-Propylcyclohexyl) cyclohexyl]-1-trifluoromethoxybenzene (PCTB) together made up 83.3% of the total EDIs in median exposure scenario of 0–6 months infant. The highest EDI value was 1.30 × 103 ng/kg bw/day, 77.1% of which was attributed to a combination of FPrBP, 4″-ethyl-2′-fluoro-4-propyl-1,1':4′,1″-terphenyl (EFPT), 2-[4'-[difluoro(3,4,5-trifluoro-2-methyl-phenoxy)methyl]-3′,5′-difluoro-[1,1′-biphenyl]-4-yl]-5-ethyl-tetrahydro-pyran (DTMPMDP), 4-[Difluoro-(3,4,5-trifluoro-2-methyl-phenoxy)-methyl]-3,5-difluoro-4′-propyl-1,1-biphenyl (DTMPMDB), 2,3-difluoro-1-methyl-4-[(trans, trans)-4′-pentyl[1,1′-bicyclohexyl]-4-yl]benzene (DMPBB) and PCTB. It's worth noting that FLCMs have higher exposure risk. Based on the threshold of toxicological concern (TTC) method, the EDI median of FPrBP (183 ng/kg bw/day) and FPCB (3.27 ng/kg bw/day) were beyond their TTC values (2.5 ng/kg bw/day) in 0–6 months infant, implying their prospective health risk. [Display omitted] • The exposure of FLCMs in infant formulas is lower than in breast milk. • FPrBP is the main fluorinated liquid-crystal monomers in infant formula samples. • FPrBP and FPCB may have potential health risk through infant formula intake. [ABSTRACT FROM AUTHOR]

As emerging organic contaminants, Polyhalogenated carbazoles (PHCZs) have caused wide concerns due to their wide distribution in the environment and dioxin-like toxicity. Nevertheless, research on the distribution and formation mechanisms of PHCZs in polluted environment of printing and dyeing plants is lacking. Here, 11 PHCZs were detected in samples from the Cao'e River, China, a typical river heavily polluted by printing and dyeing. The PHCZs concentrations in the soil, sediment, and water samples were 8.3–134.5 ng/g (median: 26.3 ng/g), 17.7–348.8 ng/g (median: 64.2 ng/g), and 1.2–41.4 μg/L (median: 4.8 μg/L), respectively. 3,6-dichlorocarbazole was the dominant congener, proved by both analysis results and formation mechanisms. PHCZ migration patterns in water-sediment systems indicated that highly halogenated PHCZs tend to be transferred to sediment. Furthermore, PHCZs are persistent, can undergo long-range transport, and pose high risks to aquatic organisms by models. PHCZs released from dye production into environment can be form through halogenation of carbazole or PHCZs formed during the dye synthesis, heating of halogenated indigo dyes, and photolysis of highly halogenated PHCZs. This is the first comprehensive study to reveal the impact of printing and dyeing plant activities on PHCZs in the environment. [Display omitted] • Pollution of PHCZs was detected in river water contaminated by industries. • Levels of PHCZs in dyes-polluted environments were significantly higher. • Printing and dyeing were the main source of PHCZ in the region. • PHCZs had similar environmental behavior as several known POPs such as PCDFs. • PHCZs were highly toxic to aquatic organisms and posed a high ecological health risk. [ABSTRACT FROM AUTHOR]

To understand the pollution status and ecological risk of polycyclic aromatic hydrocarbons (PAHs) in the sediments of the Changchun section of the Yitong River, ten (10) surface sediment samples were collected in September 2020. The distribution, source and potential ecological risk of PAHs in the sediments were studied. The results showed that the total concentration of 16 single polycyclic aromatic hydrocarbons in the sediment was 876.0-3216.1 ng/g. The average was 2319.1 ng/g, and most of the 16 PAHs were low molecular weight PAHs. Source analysis showed that the primary pollution source in the sediments of the Changchun section of the Yitong River was the incomplete combustion of bio-mass such as petroleum and coal. In addition, the ecological risk of PAHs in sediment was analyzed by the low median method of effect interval. The evaluation results showed that the content of Ace in sur-face sediment of some sampling points exceeded the median of effect interval (ERM), and the ecological risk of PAHs in the sediment of the Changchun section of the Yitong River was low. Meanwhile, the risk quotients (RQs) method results showed that the RQs values of Nap, Acy, Ace, BaA, Chr, BaP, DBA was RQ>1. The comprehensive analysis indicated that the pollution of PAHs in sediments might cause some ecological risk [ABSTRACT FROM AUTHOR]

Bio-monitoring of polycyclic aromatic hydrocarbons (PAHs) contaminants in mother milk is essential to keep mothers and infants healthy against potential risks. The current study assesses the concentration of PAHs in mother milk through a meta -analytic and systematic review approach. All the published studies up to December 2020 regarding the concentrations of various PAHs in mother milk were searched throughout major international databases such as PubMed, Scopus, and Web of Science. Moreover, the possible carcinogenic and mutagenic risks to infants were evaluated based on the BaP (benzo[a]pyrenee) equivalent dose. According to the results of 13 articles included among 936 retrieved studies, the lowest and highest concentration of PAHs was (0.125 ng/g) and (76.36 ng/g) related to benz(a)anthracenem and 1-methylnaphthalene, respectively. The highest (9.830 ng/g) and lowest (0.009 ng/g) concentration of PAHs was related to Mexico and Japan, respectively. Besides, carcinogenetic and mutagenic risk assessment of the PAHs indicated that risk pattern was different across countries. It can be concluded that the consumption of mother milk is safe and does not pose a risk due to the ingestion of PAHs to the health of infant consumers. [ABSTRACT FROM AUTHOR]

We examined the occurrence and levels of 19 legacy and emerging per- and polyfluoroalkyl substances (PFASs) in 7 species of marine bivalve molluscs collected from four coastal cities of Shandong Province, China. Perfluorooctanoic acid (PFOA) was the most prevalent component, accounting for 68.1 % of total PFASs. The total PFASs in bivalve molluscs ranged from 0.86 to 6.55 ng/g wet weight, with the highest concentration found in Meretrix meretrix L. The concentration of total PFASs in bivalve molluscs showed the following trend: clams > scallops > oysters > mussels. Estimation on the human intake of PFASs from consumption of bivalve molluscs resulted in hazard ratios (HR) ranging from 0.12 to 6.40. Five of the seven species had HR >1, indicating high exposure risks associated with PFASs. Therefore, the occurrence of PFASs in marine biota is particularly concerning and further investigations on the sources of PFASs in Shandong are warranted. • First time detection of 19 PFASs in bivalve molluscs in Shandong Province • PFASs levels in bivalve molluscs varied from 0.86 to 6.55 ng/g wet weight. • PFOA, PFBA, PFNA and PFOS were the compounds most frequently detected. • Frequent consumption of bivalve molluscs may pose health risk. [ABSTRACT FROM AUTHOR]

Coking is a main industrial emission source of polycyclic aromatic hydrocarbons (PAHs) in China. A comprehensive study was conducted of the concentrations, spatial distribution, sources, and the potential human health risks of 16 priority PAHs in agricultural soil within 2000 m of a Coking Plant in Shanxi, North China, which has been in production for more than 20 years. Diagnostic ratios were employed to identify the sources of PAHs. Toxic equivalency factors of benzo[a]pyrene were used to evaluate the health-risk of PAHs. Results showed that the total concentrations of the 16 PAHs ranged from 2297 to 9421 ng/g. The mean total concentrations of 15 relatively stable PAHs (£15PAHs) in agricultural soil around the coking plant were 6591, 4518 and 2208 ng/g at the distances of 1000, 1000~1500 and 1500~2000 m, respectively. £15PAHs decreased with the increasing distance from the emission source. The 4-5-rings PAHs of fluoranthene, pyrene, benz[a]anthracene and chrysene were the most dominant components with an average percentage contribution of 52.72%. The PAHs in soils were mainly from pyrogenic sources, especially coal combustion. The benzo[a]pyrene concentrations of 7 carcinogenic PAHs accounted for 83% of the total 15 PAHs. The £PAHs7c mainly contributed to the potential carcinogenic risk for humans, which declined with distances increasing in 2000 m. Long-term exposure to coking plants potentially induce human health risks. [ABSTRACT FROM AUTHOR]

The Soummam River, a vital watercourse in Algeria is threatened by anthropogenic activities despite its protected wetland status. This study is the first to assess sediment pollution in the Soummam River, examining levels, compositions, sources of 16 PAHs and their effects on the environment and human health. Analysis employing Principal Component Analysis (PCA) and molecular diagnostic ratios pointed to petrogenic sources, likely stemming from petroleum leaks originating from aging pipeline and vehicles, as well as pyrogenic sources arising from vehicle exhaust and biomass combustion. Environmental and health risks were assessed through risk quotients (RQ), Sediments Quality Guidelines (SQG) and Total Lifetime Cancer Risk (TLCR). Ecological risk was found to range from moderate to high, with anticipated biological impacts, while cancer risk was deemed low. Toxicity assessment, measured by TEQ, revealed that the majority of monitoring stations exceeded safe levels. Consequently, urgent action by local authorities is warranted to implement ecosystem rehabilitation measures. [Display omitted] • Concentrations of PAHs ranged from 1862.75 ng/g to 22,939.98 ng/g. • Diagnostic ratios and PCA revealed a combination of petrogenic and pyrogenic inputs. • Ecological risk was evaluated by RQ and SQG and was classified as moderate to high. • Total Life Time Cancer (TLCR) indicated a low risk. • Most of the stations exceeded the safe level for toxicity. [ABSTRACT FROM AUTHOR]

The main objectives of this study are to measure permanent organic and inorganic pollutants in detail in an area that hosts historical structures underneath and feeds the huge ecosystem with water, to reveal risk values. Total PAH concentrations in the samples ranged from 43.41 to 202.7 ng/g. Total OCP concentration ranged from 5.15 to 17.98 ng/g, while total PCB concentration ranged from 0.179 to 0.921 ng/g. PCB 28/31, 138, and 153 are the highest detected PCBs. It was found that the lake sediment reached toxic equivalent quotient (TEQ) values of 29.21 for total PAHs and 28.90 for carcinogenic PAHs. Negligible concentration risk quotient had a low to moderate ecological and toxicological risk between 12.91 and 64.42. Highest pollution index value was found 3.81 and the risk index value reached 417.4. It has been revealed that toxicologically risky components accumulate over many years even in the best-protected water resources. [Display omitted] • Phenanthrene and Naphthalene were the dominant PAHs at all sampling points. • PCB 28/31, 138, and 153 are the highest detected PCBs • DDE, DDT and DDD were found to be ecologically risky. • Highest ecological risk caused by Ag, Pb, Cu, and Ni in terms of metals • Industrial and domestic pollution are severe sources of pollution. [ABSTRACT FROM AUTHOR]

The distribution of polycyclic aromatic hydrocarbons (PAHs) and halogenated PAHs (HPAHs) in surface soils from the petroleum industrial area of the Yellow River Delta (YRD) in China were investigated. The total concentrations of 16 PAHs ranged from 19.6 to 1560 ng/g, while 22 HPAHs ranged from 2.44 to 14.9 ng/g. Moreover, a high degree of spatial distribution heterogeneity was observed for both PAHs and HPAHs, which is likely attributed to the distinct industrial activities in studied area. The combustion of biomass and petroleum were identified as primary sources of soil PAHs and HPAHs in the YRD. Furthermore, benzo[ b ]fluoranthene, benzo[ k ]fluoranthene, and benzo[ g , h , i ]perylene exhibited high ecological risks (with risk quotients of 1.47, 1.44, and 1.02, respectively) in specific sites within the YRD. Considering the high toxicity of HPAHs and their potential joint environmental effects with PAHs, continuous attention should be directed towards the environmental risks associated with both PAHs and HPAHs. [Display omitted] • Co-occurrence of PAHs and HPAHs was found in soil in Yellow River Delta. • Industrial activities resulted in spatial heterogeneity of PAHs and HPAHs in soil. • Biomass and petroleum combustion are primary sources of soil PAHs and HPAHs. • Benzo[ b ]fluoranthene poses high ecological risks in studied areas. [ABSTRACT FROM AUTHOR]

Understanding PAH and OCP distributions and sources in lakes is necessary for developing pollutant control policies. Here, we assessed the occurrence, risk, and sources of PAHs and OCPs in the sediment of Caohai Lake. The PAHs were predominantly high-molecular-weight compounds (mean 57.5 %), and the diagnostic ratios revealed that coal, biomass burning, and traffic were the sources of PAHs. HCHs (6.53 ± 7.22 ng g−1) and DDTs (10.86 ± 12.16 ng g−1) were the dominant OCPs and were primarily sourced from fresh exogenous inputs. RDA showed that sediment properties explained 74.12 % and 65.44 % of the variation in PAH and OCP concentrations, respectively. Incremental lifetime cancer risk (ILCR) assessment indicated that hazardous PAHs in Caohai Lake sediment posed moderate risks to children and adults (ILCR>1.0 × 10−4), while the risk from OCPs was low; however, the recent influx of HCHs and DDTs requires additional attention. [Display omitted] • PAHs were predominantly high molecular-weight PAHs and derived from coal, biomass burning and traffic sources. • DDTs dominated OCPs and fresh exogenous input of HCHs and DDTs should be given more attention. • PAHs in sediments pose a moderate risk to children and adults, while OCPs pose a low risk to humans. • Sediment properties affect PAHs and OCPs levels, and COPs content is mainly influenced by sediment MBC. [ABSTRACT FROM AUTHOR]

Mercury (Hg), especially methylmercury (MeHg), which is highly neurotoxic, is a global pollutant that can affect human health because of its accumulation in aquatic products. Poyang Lake, an inland lake in China, has been significantly affected by human activity, yet there is limited understanding of local mercury contamination and potential exposure pathways to humans. In this study, we explored the risks of mercury exposure by sampling sediments, plants, and aquatic organisms in the lake and surrounding areas and analyzing total Hg (THg) and MeHg levels. Sediment sampling was conducted at the main lake, rivers, rice paddies, and fishponds. Two dominant species of plants and 15 species of aquatic organisms were sampled and analyzed. We assessed the characteristics of mercury in sediments using the geo-accumulation index (I geo), mercury exposure using the biomagnification factor (BMF) and biota sediment accumulation factor (BSAF), and risks using thresholds for adverse effects. The highest THg concentrations (137.04 ± 44.3 ng g−1 dw) were detected in the main lake sediments, whereas the highest MeHg concentrations (0.47 ± 0.6 ng g−1 dw) were detected in fishpond sediments. Mercury accumulation in the main lake sediments could be assessed as contaminated (I geo > 0: 81.6%). Yellow catfish had the highest mercury concentration (THg 770.69 ± 199.7 ng g−1 dw; MeHg 741.93 ± 168.8 ng g−1 dw). Piscivores were adversely affected by carnivorous fish (50.8%), but all fish concentrations did not exceed the food safety standards recommend by China and the WHO. The mercury exposure results revealed significant Hg biomagnification and enrichment (BMF >1: 94.55%; BSAF max = 1218). Long-term monitoring of aquatic organisms is warranted. [Display omitted] • Sediments in Poyang Lake were moderately contaminated by mercury. • Fish mercury biomagnification factors were higher for methylmercury compared to total mercury. • Carnivorous fish posed the greatest risk for fish eating wildlife. • Fish mercury concentrations did not exceed food safety standards. [ABSTRACT FROM AUTHOR]

Kelp, the brown alga distributed in coastal areas all over the world, is also an important medicine food homology product in China. However, the levels and profiles of persistent organic pollutants (POPs) in kelp have not been thoroughly investigated to date. Polychlorinated biphenyls (PCBs), polybrominated diphenyl ethers (PBDEs) and emerging bromine flame retardants (eBFRs) were evaluated in 41 kelp samples from the main kelp producing areas in China. The concentrations of total PCBs, PBDEs and eBFRs were in the range of 0.321–4.24 ng/g dry weight (dw), 0.255–25.5 ng/g dw and 3.00 × 10−3-47.2 ng/g dw in kelp, respectively. The pollutant pattern was dominated by decabromodiphenyl ethane (DBDPE, 13.0 ± 11.7 ng/g dw) followed in decreasing order by BDE-209 (2.74 ± 4.09 ng/g dw), CB-11 (1.32 ± 1.06 ng/g dw). The tested results showed that kelp could reflect the pollution status of PCBs, PBDEs and eBFRs, indicating the suitability of kelp as a biomonitor of these harmful substances. Finally, the data obtained was used to evaluate human non-cancer and cancer risks of PCBs and PBDEs via kelp consumption for Chinese. Though the calculated risk indices were considered acceptable according to the international standards even in the worst scenarios, the POPs levels in kelp should be monitored continuously as a good environmental indicator. [Display omitted] • PCBs, PBDEs and eBFRs residues in the kelp samples from coastal areas of China were assessed. • The EDI of eBFRs was far higher than that of PCBs and PBDEs via kelp consumption. • Kelp can be a reliable biomonitor of POPs in coastal ecosystems. [ABSTRACT FROM AUTHOR]

A comprehensive analysis of 15 target chemical compounds (pharmaceuticals and personal care product, perfluoroalkyl compounds and industrial chemicals) were carried out to determine their concentrations in selected commercially exploited, wild caught small and medium sized pelagic fish species and their organs (Thyrsites atun (snoek) , Sarda orientalis (bonito) , Pachymetopon blochii (panga) and Pterogymnus laniarius (hottentot)) obtained from Kalk Bay harbour, Cape Town. Solid phase extraction (SPE) method based on Oasis HLB cartridges were used to concentrate and clean-up the samples. Liquid chromatography–mass spectrometry analysis of these chemical compounds revealed the simultaneous presence of at least 12 compounds in different parts of the selected fish species in nanogram-per-gram dry weight (ng/g dw) concentrations. The results revealed that perfluorodecanoic acid, perfluorononanoic acid and perfluoroheptanoic acid were the most predominant among the perfluorinated compounds and ranged between: (20.13–179.2 ng/g), (21.22–114.0 ng/g) and (40.06–138.3 ng/g). Also, diclofenac had the highest concentration in these edible fish species out of all the pharmaceuticals detected (range: 551.8–1812 ng/g). The risk assessment values were above 0.5 and 1.0 for acute and chronic risk respectively which shows that these chemicals have a high health risk to the pelagic fish, aquatic organisms and to humans who consume them. Therefore, there is an urgent need for a precautionary approach and the adequate regulation of the use and disposal of synthetic chemicals that persist in aquatic/marine environment in this province and other parts of South Africa, to prevent impacts on the sustainability of our marine environment, livelihood and lives. Image 1 • The occurrence of 15 emerging pollutants in the Kalk Bay harbour, Cape Town were investigated. • Increasing levels of perfluoroalkyl compounds in the Cape Town oceanic environs. • Fish species from Kalk Bay harbour were contaminated and may be at risk. • Total concentrations of compounds ranged from not detected to 1812 ng/g dry weight. • Diclofenac levels were highest and most frequently detected. Fifteen compounds from Kalk Bay harbour were detected in different fish species in Cape Town oceanic environs. Diclofenac levels were highest and most frequently detected. [ABSTRACT FROM AUTHOR]

Usage of neonicotinoids is common in all agricultural regions of the world but data on environmental contamination in tropical regions is scarce. We conducted a survey of five neonicotinoids in soil, water and sediment samples along gradients from crops fields to protected lowland tropical forest, mangroves and wetlands in northern Belize, a region of high biodiversity value. Neonicotinoid frequency of detection and concentrations were highest in soil (68%) and lowest in water (12%). Imidacloprid was the most common residue reaching a maximum of 17.1 ng/g in soil samples. Concentrations in soils differed among crop types, being highest in melon fields and lowest in banana and sugarcane fields. Residues in soil declined with distance to the planted fields, with clothianidin being detected at 100 m and imidacloprid at more than 10 km from the nearest applied field. About half (47%) of the sediments collected contained residues of at least one compound up to 10 km from the source. Total neonicotinoid concentrations in sediments (range 0.014–0.348 ng/g d. w.) were about 10 times lower than in soils from the fields, with imidacloprid being the highest (0.175 ng/g). A probabilistic risk assessment of the residues in the aquatic environment indicates that 31% of sediment samples pose a risk to invertebrate aquatic and benthic organisms by chronic exposure, whereas less than 5% of sediment samples may incur a risk by acute exposure. Current residue levels in water samples do not appear to pose risks to the aquatic fauna. Fugacity modeling of the four main compounds detected suggest that most of the dissipation from the agricultural fields occurs via runoff and leaching through the porous soils of this region. We call for better monitoring of pesticide contamination and invertebrate inventories and finding alternatives to the use of neonicotinoids in agriculture. Image 1 • A survey and risk assessment of neonicotinoids in Belize. • We measured neonicotinoids in soil, sediment and water in northern Belize • Neonicotinoid residue levels were highest in soils of planted crops • Frequency of residues declined from soil (68%) to sediment (47%) and water (12%) • Concentrations in soil and sediment decreased with distance to field • 31% of sediment samples may pose a risk to aquatic invertebrates by chronic exposure Neonicotinoid residues found in wetlands of a Neotropical Nature Reserve pose a risk to aquatic invertebrates. [ABSTRACT FROM AUTHOR]

Abstract The levels and distribution of synthetic musks (ADBI, AHMI, ATII, HHCB, AHTN, MX and MK) were investigated in farmland soils from the Three Northeast Provinces of China. The total concentrations of SMs ranged from 2.40 ng/g to 12.2 ng/g (dry weight). HHCB and AHTN were the main pollutants that were detected in all samples, accounting for 99.35% of the total SMs. The hazard quotients were 0.0700 and 0.102 for AHTN and HHCB, respectively. Although the results indicate there is no serious environmental impact, the detection frequency of SMs in the farmland soil is high, which demonstrated that SMs are widely used in the Three Northeast Provinces of China. Therefore, more attention should be given to synthetic musks during environment monitoring and risk assessments for their bioaccumulation, lipophilicity and persistence. Highlights • Galaxolide (HHCB) and tonalide (AHTN) were the main pollutants detected in the farmland soils. • Low ecological risks were found for HHCB and AHTN in Three Northeast Provinces of China. • Significant positive correlations were found between HHCB and AHTN (p < 0.01). [ABSTRACT FROM AUTHOR]

Abstract In this study, six alkyl esters of p-hydroxybenzoic acids (parabens) and their metabolite, 4-hydroxybenzoic acid (p-HB) were simultaneously determined in surface water and sediment from the Yellow River and the Huai River in Henan Province, China. Concentrations of ∑parabens in surface water were 3.31–55.2 ng/L in the Yellow River and 15.0–164 ng/L in the Huai River, while in the sediment, concentrations of ∑parabens were 13.3–37.2 ng/g and 16.1–31.6 ng/g, respectively. Compared with other studies, levels of parabens in the studied area were relatively high in the sediments but middle in the surface water. MeP and PrP were the most abundant parabens, and were detected in all sampling sites. Contributions of EtP, BzP, BuP, and HeP to ∑parabens were each no more than 10%. 4-Hydroxybenzoic acid was found in all samples albeit at low concentrations. Significant positive correlations among parabens suggest similar sources of parabens in the Yellow River and the HuaiRiver. Dissolved organic carbon (DOC) had an important effect on parabens in the surface water of the Yellow and Huai Rivers. Due to low dilution of discharges, high concentrations of parabens were found during moderate precipitation season as well as minimal precipitation season in surface water. However, no apparent seasonal variation of parabens in surface sediment was observed. Hazard quotients showed that the ecological risks of parabens was low in the studied area. Graphical abstract fx1 Highlights • Parabens and p-HB in the Yellow River and the Huai River were evaluated. • MeP and PrP were the most abundant parabens in surface water and surface sediment. • Apparent seasonal variation of Parabens in surface water was detected. • The ecological risk assessment of parabens in the studied area was low. [ABSTRACT FROM AUTHOR]

Abstract This work aimed to determine the concentrations of parabens and triclosan (TCS) in shellfish from coastal waters of Shenzhen, South China. A method of isotope dilution with high performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS) was used to determine TCS and five paraben analogues, including methyl paraben (MeP), ethyl paraben (EtP), propyl paraben (PrP), butyl paraben (BuP), and benzyl paraben (BeP), in 186 shellfish samples covering eight species. Concentrations of parabens and TCS were 0.13–25.5 ng/g wet weight (ww) and 7 ng/kg bw/day) and TCS (200 ng/kg bw/day), indicating no significant human health risks from shellfish consumption in the studied region. To our knowledge, this is the first report on the occurrences of parabens and TCS in shellfish products from Shenzhen coastal waters. Graphical abstract Image 1 Highlights • Levels of parabens and triclosan in shellfish from Shenzhen coastal waters. • Positive relationships among MeP, PrP, EtP, and TCS indicated similar sources. • The EDI values of parabens and TCS were much lower than the ADI values. • No significant human health risks via shellfish consumption were demonstrated. Levels of parabens and triclosan in shellfish collected from Shenzhen coastal waters indicated human influences and no human health risks via shellfish consumption. [ABSTRACT FROM AUTHOR]

This study examines the occurrence of Polycyclic aromatic hydrocarbons (PAHs) in sediment samples collected from three areas (Saronikos Gulf, Piraeus harbor, Heraklion) across the Hellenic coastline, while PAHs distribution, sources and ecotoxicological risk are evaluated. According to the detected concentrations of PAHs, the most contaminated area was Piraeus (ΣPAHs: 125 to 2720 ng/g dw), followed by Saronikos Gulf (ΣPAHs: 21.4–1820 ng/g dw) and Heraklion (4.10–230 ng/g dw). Most sampling sites clearly show evidence for "combustion" in the source, whereas the data from Piraeus harbor indicate petroleum contamination as well. The calculated Toxic Equivalence Quotient (TEQ) and Mutagenic Equivalence Quotient (MEQ) values for Saronikos Gulf and Heraklion reveal low, or no, adverse health effects to exposed biota, while the pollution picture in Piraeus port indicates that BaP is the main contributor to carcinogenic and mutagenic risk. Risk assessment regarding dermal uptake of PAHs corroborated a negligible risk. • Polycyclic aromatic hydrocarbons (PAHs) were analysed is sediment samples from Greece. • Pireaus port (PIR) was the most contaminated area, followed by Saronikos Gulf (SG) and Heraklion (HER). • PAHs occurrence in most sampling sites is attributed to combustion sources. • Pireaus harbor suggest contamination both from combustion and petroleum sources. • The ecological risk assessment reveals that sediment from SG and HER pose a lower risk compared to the sediment of PIR. [ABSTRACT FROM AUTHOR]

To understand the levels of PAHs and ecological risks to the marine environment in Laizhou Bay and Bohai Bay, 33 sediment samples were collected in the region for analysis. PAH concentrations ranged from 98.22 ng·g−1 (dw) to 239.01 ng·g−1 (dw). PAHs in the region are at low to medium pollution levels compared to studies worldwide. Diagnostic ratios and PCA indicate that PAHs are primarily sourced from fuel combustion. PAHs carried into the Bohai Sea by means of river water and sediment are more likely to settle to the seafloor as opposed to diffuse. This results in a slightly higher proportion of low-ring PAHs than high-ring PAHs. Low-ring PAHs accounted for 56 % of the total. Low-ring PAHs are key contributors to ecosystem risk. The SQGs and RQ ∑PAHs show that PAHs do not pose a considerable ecological danger within the region. • Low-ring PAHs accounted for 56 % of the total. • PAHs originate mainly from biomass and fossil fuel combustion. • Most low-ring PAHs pose a moderate ecological risk. [ABSTRACT FROM AUTHOR]

In light of the documented elevated concentrations of total mercury (Hg) and methylmercury (MeHg) in poultry originating from Hg-contaminated sites, a knowledge gap persists regarding the levels of Hg found in home-produced eggs (HPEs) and the associated dietary exposure risks in regions affected by Hg mining. To address this knowledge gap, a comprehensive investigation was undertaken with the primary objectives of ascertaining the concentrations of THg and MeHg in HPEs and evaluating the potential hazards associated with the consumption of eggs from the Wanshan Hg mining area in Southwest China. The results showed that THg concentrations in HPEs varied within a range of 10.5–809 ng/g (with a geometric mean (GM) of 64.1 ± 2.7 ng/g), whereas MeHg levels spanned from 1.3 to 291 ng/g (GM, 23.1 ± 3.4 ng/g). Remarkably, in half of all eggs, as well as those collected from regions significantly impacted by mining activities, THg concentrations exceeded the permissible maximum allowable value for fresh eggs (50 ng/g). Consumption of these eggs resulted in increased exposure risks associated with THg and MeHg, with GM values ranging from 0.024 to 0.17 µg/kg BW/day and 0.0089–0.066 µg/kg BW/day, respectively. Notably, the most substantial daily dosage was observed among children aged 2–3 years. The study found that consuming HPEs could result in a significant IQ reduction of 34.0 points for the whole mining area in a year. These findings highlight the potential exposure risk, particularly concerning MeHg, stemming from the consumption of local HPEs by residents in mining areas, thereby warranting serious consideration within the framework of Hg exposure risk assessment in mining locales. [Display omitted] • Elevated THg and MeHg concentrations were detected in HPEs from Hg mining areas. • Nearly half of the HPEs samples exhibited higher THg concentrations than 50 ng/g. • HPEs is a significant pathway for human exposure to MeHg in mining areas. • HPEs eating can cause certain intelligence impairment in children in mining areas. [ABSTRACT FROM AUTHOR]

Abstract Melamine-based resins are used extensively in laminates, plastics, coatings, glues, and dinnerware. Little is known, however, about the occurrence of melamine and its derivatives in the environment. In this study, a nationwide survey of melamine and its derivatives, namely ammeline, ammelide, and cyanuric acid, was conducted, using archived sewage sludge samples collected from 68 wastewater treatment plants in the United States (U.S.). The sum concentrations of four target compounds in sludge ranged from 34 to 1800 ng/g dry weight (dw), with a mean concentration of 240 ng/g dw; melamine (46%) and cyanuric acid (40%) collectively accounted for 86% of the total mass of analytes. No significant geographical variation in the concentrations of melamine and its derivatives in sewage sludge was found. The estimated emission of melamine and its derivatives via land-application of sludge was approximately 1600 kg/yr in the U.S. The hazard quotient values for melamine in sludge-amended soils ranged from 2.2 × 10−5 to 4.4 × 10−3, indicating that the current levels of melamine in sludge pose a minimal risk to the soil environment. Graphical abstract Image 1 Highlights • Melamine and its derivatives were consistently detected in sludge samples. • ∑Melamine concentrations in sludge ranged 34–1800 ng/g dry weight. • Melamine was prevalent in sludge, followed by cyanuric acid. • Emission of ∑melamine through U.S. biosolids was estimated at 1600 kg/yr. Melamine and cyanuric acid are widely present in sewage sludge collected across the United States. [ABSTRACT FROM AUTHOR]

Abstract A nationwide survey, including 75 sludge samples and 18 wastewater samples taken from different wastewater treatment plants (WWTPs) from 23 cities, was carried out to investigate the occurrence and composition profiles of polycyclic aromatic hydrocarbons (PAHs) in China. In total, the concentrations of ∑ 16 PAHs in sludge ranged from 565 to 280,000 ng/g (mean: 9340 ng/g) which was at a moderate level in the world. The composition profiles of PAHs were characterized by 3- and 4-ring PAHs in textile dyeing sludge and 4- and 5-ring PAHs in domestic sludge. Significant variations in regional distribution of PAHs were observed. Both the principal components analysis and diagnostic ratios revealed that vehicle exhaust, coal and natural gas combustion were the main sources of PAHs in China. The estimated concentrations of PAHs were 3820 ng/L and 1120 ng/L in influents and effluents of the WWTPs, respectively. The high toxic equivalent quantity (TEQ) values of PAHs are ascribed to the high PAH levels. Risk quotient values (RQs) in sludge indicated that there was low potential risk to soil ecosystem after sludge had been applied one year except for indeno [1,2,3-cd]pyrene (IcdP) detected in Huaibei, Anhui province. Graphical abstract Image 1 Highlights • 75 sludge samples and 18 wastewater samples from WWTPs were collected in China. • A distinct geographical distribution of PAHs was observed. • The concentrations of PAHs in influents and effluents of China were estimated. • There were low risks to soils when sludge had been applied after one year. This is the most comprehensive study to investigate the occurrence and composition profiles of PAHs in sewage sludge and wastewater in China. [ABSTRACT FROM AUTHOR]

Distribution characteristics, potential sources, and possible biological hazards of polycyclic aromatic hydrocarbons (PAHs) were examined in intertidal surface sediments of Zhelin Bay, the biggest mariculture base of eastern Guangdong Province, Southern China. The total PAH concentrations ranged from 8.05–51.32 ng/g (dry weight) with an average of 29.23 ng/g, which is beneath the documented concentrations in intertidal sediments gathered from various bays across the globe. The composition of PAHs was distinguished by high molecular weight (HMW, 4–6 rings) PAHs, with phenanthrene (PHE), fluoranthene (FA), and benzo(b)fluoranthene (BbFA) established as predominant components. Principle component analysis along with multivariate linear regression discovered that liquid fossil fuel combustion and coal/wood combustion contribute to 60.23% and 39.77% of PAHs in Zhelin Bay's intertidal sediments, respectively. Overall, surface sediments of Zhelin Bay have an 8% increased incidence of adverse biological effects due to PAH contamination, based on the mean probable effect level quotient. [ABSTRACT FROM AUTHOR]

The COVID-19 pandemic has led to children using polymeric FFP2 and polymeric surgical masks on a daily basis. Children often bite and suck on such masks as they wear them closed to their mouths. In this work, the migration of contaminants from printed and unprinted children's masks to a saliva simulant has been studied. Liquid chromatography coupled to ion-mobility quadrupole time-of-flight mass spectrometry has been used for the detection and identification of non-volatile migrants. An orthogonal projection to latent structures – discriminant analysis (OPLS-DA) was applied to compare the data from the printed masks against the data from the unprinted ones. Headspace solid phase microextraction coupled to gas chromatography mass spectrometry was used to assess the migration of volatile compounds. Thirteen compounds were found in the masks with concentrations ranging from 5 ng/g to 254 ng/g. Toluene, chlorobenzene, irganox 1076 and 2-(2-butoxyethoxy)ethyl acetate were all found to migrate from the masks studied. Moreover, differences between the migrants from printed and unprinted FFP2 masks were found. Octocrylene, 4-(dimethylamine)benzoate, methyl 3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate and tris(3-methylphenyl)phosphate were found to migrate only from printed masks. Toluene that migrated from all the masks studied and tris(3-methylphenyl)phosphate, that migrated only from printed masks, have been listed as hazardous priority substances. • The migration of contaminants from printed and unprinted masks to a saliva simulant has been studied. • Thirteen compounds were discovered to have migrated in the saliva simulant. • Differences between the migrants from printed and unprinted masks were found. • Two migrants, toluene and tris(methylphenyl)phosphate, were categorized as hazardous priority substances. [ABSTRACT FROM AUTHOR]

Metalaxyl (MET) and myclobutanil (MYC) are two widely used chiral fungicides that may pose health risks to non-occupationally exposed populations. Here, the two fungicides were enantiomer-specific quantified in the dietary food and urine of residents in an Eastern China city, to determine the exposure and excretion of these contaminants in different populations. Results indicate that residues of MET and MYC varied with different food items at 0.42–0.86 ng/g fresh weight (FW) and 0.18–0.33 ng/g FW, respectively. In urine samples, the residual levels after creatinine adjusting (CR) ranged from 10.2 to 1715.4 ng/g CR for MET and were below the detection limit up to 320.7 ng/g CR for MYC. Significant age- and gender-related differences were separately found in urinary MET and MYC of different populations. Monte-Carlo simulations suggested that children had higher daily dietary intake (DDI) but lower urinary excretion (DUE) rates than youths, and thus may suffer higher body burdens. The residues of antifungally ineffective enantiomers (S -MET and R -MYC) were slightly higher than their antipodes in foods. Moreover, the enantiomer-selective urinary excretion resulted in higher retention of S -MET and R -MYC in the human body. Our results suggest that both dietary intake and urinary excretion should be enantiomer-specifically considered when assessing the exposure risk and body burden of chiral fungicides in the non-occupationally exposed population. Furthermore, substitutive application of enantiomer-enriched fungicide formulations can not only benefit the antifungal efficacy but also be safer for human health. [Display omitted] • Metalaxyl and myclobutanil were enantiomer-specifically detected in food and urine. • Urinary excretion of metalaxyl and myclobutanil were age- and gender-dependent. • Children intake more metalaxyl and myclobutanil but excrete less than youths. • Antifungally ineffective enantiomers brought extra burden to the human body. [ABSTRACT FROM AUTHOR]

Polychlorinated biphenyls (PCBs) and organochlorine pesticides (OCPs) were studied in the Nile Delta area of Egypt's southern Mediterranean for their environmental impacts, probable sources, and ecological risk assessment. Using the Gas Chromatography Triple Quadrupole technique, the residues of 16 OCPs and 18 PCBs were determined. The total OCPs content in the seawater and sediment samples ranged from 0.108 to 10.97 μg/L and 0.301 to 5.268 ng/g, respectively, while the PCBs residues had values between 0.808 and 1069.75 μg/L in seawater and between not detected and 575.50 ng/g in sediment samples. The findings of the risk evaluation showed that, except for endosulfan-I, OCPs caused little harm in seawater. However, PCB180, PCB153, PCB156, PCB126 and PCB138 posed a comparatively significant risk. The concentration of DDTs was higher than the effect range low and threshold effect level but remained below the effect range median and probable effect level, posing a minimal ecological concern. • First PCBs and OCPs study in water–sediment of Nile Delta, southern Mediterranean • Residues of 16 OCPs and 18 PCBs were determined from seawater and sediment samples. • Except for endosulfan-I, OCPs caused little harm in seawater. • PCB180, PCB153, PCB156, PCB126 and PCB138 posed ecological risk concern. [ABSTRACT FROM AUTHOR]

Information on the occurrence of organobrominated compounds in bivalves from Tunisia is scarce. To the best of our knowledge, this is the first report of these compounds in clams from Tunisia. The aim of this study is to measure natural and synthetic organobrominated compound concentrations and evaluate congener distribution and pollution sources in a clam species ( Ruditapes decussatus ) from three sites of the Bizerte Lagoon. Total synthetic organobrominated pollutant levels in clam ranged from 34.8 to 188 ng g − 1 lw. For natural organobrominated compounds, concentrations varied from 18.2 to 49.5 ng g − 1 lw. Total PBDE and MeO-PBDE concentrations in clams from the Bizerte Lagoon were similar or slightly lower than those reported for other species from other locations around the world. The health risks associated with the consumption of this species were assessed and posed no threat to public health concerning PBDE intakes. [ABSTRACT FROM AUTHOR]

The polycyclic aromatic hydrocarbons (PAHs) concentrations in the water, suspended particulate matter (SPM) and sediment from the middle reaches of Huai River were analyzed by a gas chromatograph-mass spectrometer (GC-MS). The mean concentrations for the sum of 16 PAHs (∑ 16 PAHs) in the water, SPM and sediment were 1204 ng/L, 3192 ng/g (dry weight; dw), and 7955 ng/g (dw), respectively. Along the vertical profiles of water columns, higher ∑ 16 PAHs levels were seen in surface and bottom water layers and co-located SPM. The PAHs distribution in water and SPM is found to be controlled by organic carbon. Based on the statistic correlations of the organic carbon normalized partition coefficients (lgK OC ) and octanol-water partition coefficient (lgK OW ), we observed that the calculated partition coefficients do not increase as large as that would be expected from the increase of hydrophobicity. The principal component analysis suggests that coal combustion and the petroleum refinery were the primary PAHs contributors in the studied water-SPM-sediment system. The high ecological risks of PAHs in studied system highlight the urgent needs for remedial actions. [ABSTRACT FROM AUTHOR]

The present study extrapolates the assessment and characterization of a barely studied region, the Gulf of Kutch, (near Jamnagar), Gujarat, India, in terms of PAH exposure, adverse effects caused by them, and various toxicological indices showing the catastrophic effects of their elevated concentrations. ΣPAH concentration in the site ranged from 118,280 to 1,099,410 ng g − 1 dw, with a predominance of 2–3-ring PAHs (79.09%) as compared to 4–5- and 6-ring PAHs (20.91%). The concentrations of carcinogenic PAHs were found to be between 8120 and 160,000 ng g − 1 dw, with a mean of 63,810 ng g − 1 dw, which is much higher than normal acceptable values. The toxic equivalent quotient for 6CPAHs ranged from 150.47 to 26,330 ng g − 1 BaP eq, encompassing 50.63% of ΣPAH toxicity. This toxicological profile of the present study site would be of paramount importance as it offers fresh information regarding the load of legacy pollutants such as PAHs and the inputs and methods to cope with their extremely high concentrations in less explored marine habitats. [ABSTRACT FROM AUTHOR]

To study the distribution, sources, ecological/health risks, and the impact of regional economic variations on polycyclic aromatic hydrocarbons (PAHs) contaminations along the coast of the Yellow Sea in China, sediments from a broad coastal coverage were collected and analyzed. The total contents of 16 priority PAHs varied between 1.4 and 1675.9 ng/g except in the site of H18 (3191.4 ng/g) adjacent to Qingdao City, with an average value of 295.7 ng/g. PAH pollution along the coast presented a distinctive geographical feature, which was closely linked to local human activities, such as Rongcheng with industrial zones and aquacultural areas, and Yancheng Wetland with developed aquaculture. The source analysis results indicated that PAHs were mainly from pyrolytic sources, with smaller contributions from petroleum spills and combustion. Risk assessment suggested that PAH pollution along the Yellow Sea coast showed negligible biological risks and health risks in most areas. [Display omitted] • Sedimental PAHs along the whole Yellow Sea coast in China were detected. • Distinctive characteristics on PAHs pollution related to the local human activities. • PAHs were mainly from pyrolytic sources. • PAHs pollution showed negligible biological risks and health risks in most areas. [ABSTRACT FROM AUTHOR]

[Display omitted] • First comprehensive investigation and assessments of topsoil Hg in Central Asia. • Topsoil THg concentrations exhibited obvious differences among various landscapes. • High THg concentrations were found in the capital cities/urban clusters. • Topsoils in densely-populated areas were contaminated by Hg and had ecological risks. • Topsoil Hg posed no unacceptable health risk to both adults and children. Central Asia is one of the largest arid areas on earth, yet little is known about the concentration levels and risks of mercury (Hg) in the soils of this region. In this study, extensive sampling of topsoils (0–10 cm) from representative landscapes was carried out over Central Asia (i.e., Tajikistan, Uzbekistan, and Kyrgyzstan). The total mercury (THg) concentrations in topsoils varied widely from 1.6 to 908.0 ng/g, with high values observed in samples collected in the capital cities and urban areas. Topsoil THg concentrations among different landscapes showed a decreasing order of urban (79.8±184.0 ng/g) > woodland (27.3±28.9 ng/g) > grassland (20.6±15.9 ng/g) > farmland (18.3±9.5 ng/g) > desert (12.3±8.0 ng/g). High THg concentrations were found in the capital cities/urban clusters, followed by a gradual decrease towards the peripheries. THg concentrations were found to be negatively correlated with the distance from the sampling sites to their nearest cities, indicating that anthropogenic emissions significantly influenced the spatial distribution of topsoil Hg. A significant correlation between THg concentrations and topsoil total organic carbon (TOC) contents was also observed, suggesting that TOC played an essential role in the spatial distribution of topsoil Hg. The assessments of pollution and potential ecological risk suggested that topsoils in highly densely-populated areas were contaminated by Hg and had higher degrees of potential ecological risks. The health risk assessment results showed that the exposure risk of topsoil Hg to children was higher than that to adults. Fortunately, there was no unacceptable human health risk of topsoil Hg. This study clarified the spatial distribution and risks of Hg in the Central Asian topsoils, offering new insight into the risk prevention and control of soil Hg. [ABSTRACT FROM AUTHOR]

Organochlorine pesticides (OCPs) and polycyclic aromatic hydrocarbons (PAHs) threaten the environment due to their wide environmental resistance. Environmental paradigms coexist along the Negro River (NR) in Argentina, South America, which flows to the sea below the latitude of 40o S; however, this is the first environmental assessment of OCPs and PAHs in water of the NR for more than 15 years. With 21 sampling sites covering a range of 600 km of river extension, we assessed 16 OCPs and 16 PAHs in suspended particulate material (SPM) with regard to their levels, seasonality, sources, and potential biological risk assessment. Using gas chromatography–mass spectrometry and gas chromatography coupled with electron capture detection, we found an overall mean value for Σ 16 OCPs of 648.56 ng. g−1, d.w. Despite a ban spanning 25 years, an increasing trend of accumulation of hexachlorocyclohexanes (HCHs) and endosulfan was shown in the lower valley. The ɑ-HCH/ɤ-HCH and β-HCH/(ɑ + ɤ)-HCH ratios indicated a prevalent usage of technical HCH over lindane and recent HCH inputs. The most abundant compound, α-endosulfan, averaged 141.64 ng. g−1, d.w. and DDX (Σ 4,4′-DDE, 4,4′-DDD, and 4,4′-DDT) averaged 99.98 ng. g−1, d.w. Winter OCP loads in the NR reflected the runoff of the heaviest pesticide application period. We estimated the total discharge of DDT into the Atlantic ocean was 96 g.day−1, added to 458 g of HCHs and 257 g of endosulfans (ɑ + β + epoxide) adsorbed by the SPM. PAHs occurred widely along the river (38.83 ± 43.52 μg. g−1) and the highest levels coincided with locations with marked anthropogenic-related activity, such as petroleum/gas exploitation facilities. Risk quotient analysis showed a low risk posed by OCPs, but a high risk of potential effects on biota posed by the PAHs, highlighting the need for mitigation measures. [ABSTRACT FROM AUTHOR]

We investigated distribution, sources, and potential risks of polycyclic aromatic hydrocarbons (PAHs) in the surface sediments from the largest mariculture base in the eastern part of the province of Guangdong in southern China. Total concentrations of ∑ PAHs were 29.38–815.46 ng/g (dry weight), with a mean of 421.48 ng/g. The composition of PAHs was characterized by an abundance of low molecular weight PAHs (2–3 benzenoid ring), and Phenanthrene (PHE), Anthracene (AN) and Fluoranthene (FA) were the predominant constituents. PAHs in this area appear to have mainly originated from petroleum sources and the combustion of grass, wood, and coal. PAHs in surface sediments of Zhelin Bay had a 9% incidence of causing adverse biological effects on aquatic organisms, according to the mean effects range–median quotient. [ABSTRACT FROM AUTHOR]

The distribution, inventory, and potential risk of organochlorine pesticides (OCPs), including Hexachlorocyclohexanes (HCHs) and Dichlorodiphenyltrichloroethanes (DDTs), and their correlation with soil properties and anthropogenic factors were investigated in soils of the Campanian Plain. The total concentrations of HCHs and DDTs ranged from 0.03 to 17.3 ng/g (geometric mean: GM = 0.05 ng/g), and 0.08–1231 ng/g (GM = 14.4 ng/g), respectively. In general, the concentration of OCPs in farmland and orchards was higher than on land used for non-agricultural purposes. There are significant differences in the concentration of OCPs in the soils across the region, more specifically, the Acerra-Marigliano conurbation (AMC) and Sarno River Basin (SRB) are recognized as severely OCP-contaminated areas. The recent application of technical HCHs and DDTs in large quantities appears unlikely in light of the ratio of α -HCH/ β -HCH and p,p ′-DDT/ p,p ′-DDE, and the prohibition of the use of these chemicals in Italy nearly forty years ago. The clear correlation between the concentration of DDTs and organic carbon suggests a typical secondary distribution pattern. The mass inventory of OCPs in soils of the Campanian Plain is estimated to have a GM of 17.3 metric tons. There is no clear evidence linking the impact of geographical distribution of OCPs on the incidence of cancer, and the 95% confidence interval of total incremental lifetime cancer risk (TILCR) data falls below the internationally accepted benchmark value of 1 × 10 −5 . [ABSTRACT FROM AUTHOR]

This study assessed the tissue distribution, dietary intake, and potential health risks of eight OPPs in Pomadasys commersonnii (Spotted grunter) and Mugil cephalus (Flathead mullet) from the Sundays and Swartkops estuaries in South Africa. The highest concentration in fish tissues was found in muscles of M. cephalus (178 ± 80.4 ng/g ww) and P. commersonnii (591 ± 280 ng/g ww) from Sundays Estuary. The ∑ 6 OPPs concentration in muscles from both fish species was higher in muscles than in the gills with fenitrothion dominating the distribution profile. Results from the path analysis indicate that lipid, weights, and length of the fish species do not influence the concentration of OPPs in the studied fish species. The calculated hazard ratios, which represent the non-carcinogenic risks, were less than one for all OPPs, indicating that the concentration of OPPs detected in fish muscles had negligible consequences on human health. [Display omitted] • Six OPPs were detected in tissues of both fish species. • Higher OPPs levels were found in muscles compared to gills. • Fenitrothion was the dominant pesticides. • Paths analysis showed fish physical parameters do not influence ∑ 6 OPPs occurrence. • No non-cancer risk was associated with the consumption of both fish species. [ABSTRACT FROM AUTHOR]

This work analyzed the distribution characteristics, sources, and corresponding environmental risks of 10 organochlorine pollutants (OCPs) in soil samples from 13 stations on the Fildes Peninsula and Adelaide Island in Antarctica in 2020. Results showed that the total amount of OCP residues in the study area ranged from N.D. to 2.66 ng·g−1 with an average concentration of 0.90 ng·g−1. Six organochlorine pesticides were detected, and the residue level of DDTs was slightly lower than that of HCHs. The residues of HCHs were mainly γ-HCH and those of DDTs were mainly O, P′-DDT. Source analysis revealed that the residues mainly originated from atmospheric transport and human activities. Environmental risk analysis showed that in the study area, the residues of HCHs and DDTs were present at low levels, and their ecological risk was low. • Six OCPs were detected in the topsoil of Fildes Peninsula and Ardley Island. • The OCPs mainly originated from atmospheric transport and human activities. • OCPs in this region were at low ecological risk. [ABSTRACT FROM AUTHOR]

Home and personal care products (HPCPs) including biocides, benzotriazoles (BTs) and ultraviolet (UV) filters are widely used in our daily life. After use, they are discharged with domestic wastewater into the receiving environment. This study investigated the occurrence of 29 representative HPCPs, including biocides, BTs and UV filters, in the riverine environment of a rural region of South China where no wastewater treatment plants were present, and assessed their potential ecological risks to aquatic organisms. The results showed the detection of 11 biocides and 4 BTs in surface water, and 9 biocides, 3 BTs and 4 UV filters in sediment. In surface water, methylparaben (MeP), triclocarban (TCC), and triclosan (TCS) were detected at all sites with median concentrations of 9.23 ng/L, 2.64 ng/L and 5.39 ng/L, respectively. However, the highest median concentrations were found for clotrimazole (CLOT), 5-methyl-1H-benzotriazole (MBT) and carbendazim (CARB) at 55.6 ng/L, 33.7 ng/L and 13.8 ng/L, respectively. In sediment, TCC, TCS, and UV-326 were detected with their maximum concentrations up to 353 ng/g, 155 ng/g, and 133 ng/g, respectively. The concentrations for those detected HPCPs in surface water and sediment were generally lower in the upper reach (rural area) of Sha River than in the lower reach of Sha River with close proximity to Dongjiang River ( P t -test <0.05), indicating other input sources of HPCPs in the lower reach. Biocides showed significantly higher levels in surface water in the wet season than in the dry and intermediate seasons. Preliminary risk assessment demonstrated that the majority of HPCPs monitored represented low risk in surface waters. There are potentially greater risks to aquatic organisms from the use of TCS and TCC in the wet season than in dry and intermediate seasons in surface waters. This preliminary assessment also indicates potential concerns associated with TCC, TCS, DEET, CARB, and CLOT in sediments, although additional data should be generated to assess this fully. Thus future research is needed to investigate ecological effects of these HPCPs on benthic organisms in sediment of rural rivers receiving untreated wastewater discharge. [ABSTRACT FROM AUTHOR]

The study investigated the occurrence of polycyclic aromatic hydrocarbons (PAHs) in the surface sediment from eleven sites in Yangpu Bay, China in December 2013 (winter) and July 2014 (summer). The 16 US EPA priority PAHs were found in the range of 1583.2–5701.7 ng/g dry weights with an average of 3134.7 ± 1241.3 ng/g in winter and ranged from 2161.8 to 4527.2 ng/g with an average of 3016.6 ± 748.0 ng/g in summer, respectively. The concentrations of the PAHs tended to be relatively high in comparison with other areas from the literatures. The identification using molecular indices analysis indicated that the PAHs originated mainly from pyrogenic and petrogenic sources in most of the sites. According to principle component analysis–multiple linear regression (PCA/MLR) for their source apportionment, the main sources of PAHs were vehicle emissions, petroleum products and biomass combustion. The risk assessment using international sediments quality guidelines and sediments quality criteria indicated that several PAHs, such as Nap, Flu, Phe, Ace, Acy and BghiP in most of the sites would potentially affect organisms in Yangpu Bay. [ABSTRACT FROM AUTHOR]

Concentrations of 14 organophosphorus insecticides (OPs) were measured in Apis mellifera L. (European honeybee) and hive matrices (honey and bee bread). Samples were collected from seven randomly selected colonies in central Saskatchewan during the summer of 2013. LC-MS/MS was used to identify and quantify individual OP by use of a modified quick easy cheap effective rugged safe (QuEChERS) method. Diazinon, dimethoate, and chlorpyrifos-oxon were the only OPs detected in honey with mean concentrations of 0.3, 1.5, and 0.2 ng/g, wet mass (wm), respectively. Fenamiphos, chlorpyrifos, and chlorpyrifos methyl were the only OPs detected in bee bread, with mean concentrations of 0.4, 2.7, and 15.8 ng/g, wm, respectively, while ethoprop, malathion, and dichlorvos were the only OPs detected in bees with mean concentrations of 1.4, 3.7, and 889.2 ng/g, wm, respectively. Total hazard quotients (HQs), based on lethality of bees exposed to OPs in honey and pollen consumed by bees ranged from 0.01 to 0.06 and based on lethality of bees from direct exposure to OPs ranged from 0.3 to 0.4 which suggests little hazard of OPs to Saskatchewan beehives. [ABSTRACT FROM AUTHOR]

In this study, 54 sediment samples were collected from the Pearl River Estuary (PRE) in Southern China to study the spatial distribution and patterns of PFASs in this region. PFAS concentrations in the sediment samples ranged from nd (below detection limit) to 2.41 ng g −1 dw (dry weight) with an average value of 0.79 ng g −1 dw. PFAS concentrations were higher at the nearshore sampling sites than in the others. Perfluorobutanesulfonate (PFBS) and perfluorohexanesulfonate (PFHxS) were the two dominant compounds among the target PFASs, which may be due to their production and use as PFOS substitutes in the Pearl River Delta (PRD) areas. Significant linear relationships were found between total PFAS concentrations and total organic carbon (TOC) ( R = 0.30, p < 0.05). The preliminary environmental risk assessment indicated that PFOS and PFOA in the regional sediments posed no significant ecological risk to the benthic organisms at present levels. [ABSTRACT FROM AUTHOR]

Sources and ecological risk of sixteen priority PAHs in surface sediments from Bohai Sea (BS) and northern part of the Yellow Sea (NPYS) were investigated. The total concentrations of PAHs varied in ranges 149.24–1211.81 and 148.28–907.47 ng/g for BS and NPYS, respectively. Principal component analysis-multiple linear regression (PCA–MLR) suggested that coal combustion, vehicular emission and coke oven could be the primary PAH contributors, accounting for 56.6%, 29.2% and 14.2% of PAH concentrations, respectively. Analysis with sediment quality guidelines (SQGs) indicated that acenaphthylene, fluorene, phenanthrene, fluoranthene, pyrene and dibenzo(a,h)anthracene may occasionally cause adverse biological effects in some stations. Organic carbon (OC)-normalized analysis and mean effects range-median quotient (M-ERM-Q) suggested that the combined ecological risk of PAHs was generally low. The toxic equivalent concentrations of carcinogenic PAHs were 12.87–64.6 ng/g-BaP eq and 5.95–68.80 ng/g-BaP eq in BS and NPYS, respectively, suggesting low carcinogenic risk for both BS and NPYS. [ABSTRACT FROM AUTHOR]

Background: Manganese, an essential micronutrient, has been found in lower concentrations among women with preeclampsia in cross-sectional and case-control studies without establishment of a temporal relationship.Methods: We evaluated the prospective association of manganese (in red blood cells) in first trimester of pregnancy with incidence of preeclampsia (ascertained by reviewing medical records) among 1,312 women in eastern Massachusetts (Project Viva, 1999-2002). We used log-binomial regression to examine the manganese-preeclampsia relationship, adjusting for maternal age, race/ethnicity, parity, prepregnancy body mass index, blood pressure, and hematocrit.Results: The median (25th, 75th percentile) manganese concentrationin red blood cells was 16.2 ng/g (13.1, 20.4) and 48 (4%) women developed preeclampsia. We observed an inverse dose-response relationship between manganese and preeclampsia. Compared with women in the lowest tertile, women in the middle manganese tertile had 0.81 times the risk of preeclampsia (95% CI: 0.43, 1.5) and those in the highest tertile had 0.50 (95% CI: 0.25, 0.99) times the risk.Conclusions: Our results provide insight into a potentially modifiable way to prevent preeclampsia. [ABSTRACT FROM AUTHOR]