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The ingestion of fruits containing perfluoroalkyl acids (PFAAs) presents potential hazards to human health. This study aimed to fill knowledge gaps concerning the tissue-specific distribution patterns and bioaccumulation behavior of PFAAs and their isomers, alternatives, and precursors (collectively as per-/polyfluoroalkyl substances, PFASs) within citrus trees growing in contaminated fields. It also assessed the potential contribution of precursor degradation to human exposure risk of PFASs. High concentrations of total target PFASs (∑PFASstarget, 92.45–7496.16 ng/g dw) and precursors measured through the total oxidizable precursor (TOP) assay (130.80–13979.21 ng/g dw) were found in citrus tree tissues, and short-chain PFASs constituted the primary components. The total PFASs concentrations followed the order of leaves > fruits > branches, bark > wood, and peel > pulp > seeds. The average contamination burden of peel (∑PFASstarget: 57.75%; precursors: 71.15%) was highest among fruit tissues. Bioaccumulation factors (BAFs) and translocation potentials of short-chain, branched, or carboxylate-based PFASs exceeded those of their relatively hydrophobic counterparts, while ether-based PFASs showed lower BAFs than similar PFAAs in above-ground tissues of citrus trees. In the risk assessment of residents consuming contaminated citruses, precursor degradation contributed approximately 36.07% to total PFASs exposure, and therefore should not be ignored.

Perfluoroalkyl acids (PFAAs) are contaminants of global concern, and the inadvertent consumption of PFAA-contaminated crops may pose a threat to public health. Therefore, systematically studying their source tracing, bioaccumulation prediction and risk assessments in crops is an urgent priority. This study investigated the source apportionment and transport of PFAAs and novel fluorinated alternatives (collectively as per- and polyfluoroalkyl substances, PFASs) from factories to agricultural fields in a fluorochemical industrial region of China. Furthermore, bioaccumulation specificities and prediction of these chemicals in different vegetables were explored, followed by a comprehensive risk assessment from agricultural fields to dinner plates which considered precursor degradation. A positive matrix factorization model revealed that approximately 70 % of PFASs in agricultural soils were derived from fluorochemical manufacturing and metal processing. Alarming levels of ∑PFASs ranged 8.28–84.3 ng/g in soils and 163–7176 ng/g in vegetables. PFAS with short carbon chain or carboxylic acid group as well as branched isomers exhibited higher environmental transport potentials and bioaccumulation factors (BAFs) across a range of vegetables. The BAFs of different isomers of perfluorooctanoic acid (PFOA) decreased as the perfluoromethyl group moved further from the acid functional group. Hexafluoropropylene oxide dimer acid (GenX) showed relatively low BAFs, probably related to its ether bond with a high affinity to soil. Vegetables with fewer Casparian strips (e.g., carrot and radish), or more protein, possessed larger BAFs of PFASs. A bioaccumulation equation integrating critical parameters of PFASs, vegetables and soils, was built and corroborated with a good contamination prediction. After a total oxidizable precursors (TOP) assay, incremental perfluoroalkyl carboxylic acids (PFCAs) were massively found (325–5940 ng/g) in edible vegetable parts. Besides, precursor degrada

The occurrence of endocrine disrupting chemicals (EDCs) in the aquatic environment is a global concern. In this study, we employed two different passive samplers Diffusive Gradients in Thin-films (DGT) and Chemcatcher for in situ measurement of 8 phenolic EDCs in the East River of the Pearl River system over one-year. These data were assessed alongside results from traditional grab sampling. Six chemicals (4tOP, 4NP, BPA, E1, EE2 and DES) were regularly detected in the water samples, of which the three phenols (i.e. 4tOP, 4NP and BPA) were in all samples and at high concentrations (0.4–1040 ng/L for 4tOP, 2.6–58500 ng/L for NP and 11.4–123300 ng/L for BPA). Fewer target chemicals were detected in both passive samplers, with only 4tOP, 4NP and BPA found in most samplers; E1 and DES were occasionally measurable above detection limits. The higher (by about a factor of 2–3) measurements provided by DGT compared to Chemcatcher could be attributed to the effect of the diffusive boundary layer on Chemcatcher uptake or the strong adsorption of target chemicals on the Chemcatcher PES filter. The temporal trends of EDC monthly loadings indicated that they were from different sources and that WWTPs were not effective in EDC removal and/or there was still some untreated wastewater discharged into the rivers.

Industrial development has brought China both opportunities and challenges since the reform and opening up in 1978. Spatial and temporal analysis showed that rapid industrialization has made eastern China under a more serious pollution stress. The most serious effects of industrial pollution were reflected in aquatic and soil ecosystem degradation, and damage can be observed from species, population, and community to ecosystem level. Public consciousness about contaminated sites rose from 2004 leading to greater efforts in ecological remediation, monitoring, and risk governance. Considerable efforts are still needed in expanding the extent and breadth of monitoring to explore where the greatest ecological risks lie and how to control them. Ecology of industrial pollution has become a popular discipline in China and will be further developed to help achieve the Sustainable Development Goals. Future research for a better ecological risk management should be focused on multi-media transfer and effects of mixed pollutants, mechanisms for clean energy and material flow, and integration of ecological risk with human health risk.

To date limited information's are available concerning unintentional productions, screening, profiling, and health risks of polychlorinated naphthalenes (PCNs) in ambient environment and occupational environment. Literature reveals that dust is a neglected environmental matrix never measured for PCNs. To our knowledge, this is the first study to investigate the concentrations and health risks of PCNs in indoor dust, air, and blood of major e-waste recycling hubs in Pakistan. Indoor air (n = 125), dust (n = 250), and serum (n = 250) samples were collected from five major e-waste hubs and their vicinity to measure 39 PCN congeners using GC-ECNI-MS. ∑ 39PCN concentrations in indoor air, dust, and serum (worker > resident > children) samples ranged from 7.0 to 9583 pg/m 3, from 0.25 to 697 ng/g, and from 0.15 to 401 pg/g lipid weight, respectively. Predominant PCN congeners in indoor air and dust were tri- and tetra-CNs, while tetra- and penta-CNs were dominant in human serum samples. The higher PCNs contribution was recorded at the recycling units, while the lower was observed at the shops of the major e-waste hubs. Higher contribution of combustion origin CNs in air, dust and human samples showed combustion sources at the major e-waste hubs, while Halowax and Aroclor based technical mixture showed minor contribution in these samples. Mean toxic equivalent (TEQ) concentrations of PCNs were 2.79E +00 pg-TEQ/m 3, 1.60E −02 ng-TEQ/g, 8.11E −01 pg-TEQ/g, 7.14E −01 pg-TEQ/g, and 6.37E −01 pg-TEQ/g for indoor air, dust, and serum samples from workers, residents, and children, respectively. In our study, CNs- 66/67 and −73 in indoor air, dust, and human serum were the great contributors to total TEQ concentrations of PCNs. This first base line data directs government and agencies to implement rules, regulation to avoid negative health outcomes and suggests further awareness in regard of provision of proper knowledge to the target population. Due to lack of data on production

Perfluoroalkyl substances (PFASs) have become a recognized concern due to their mobility, persistence, ubiquity and health hazards in the environment. In this study, ten types of vegetables and three types of grain crops were collected in two open-air fields with different distances (0.3 km, 10 km) from a mega fluorochemical industrial park (FIP), China. Bioaccumulation characteristics of PFASs in light of crop types and organs were explored, followed by analyzing human exposure and risks to local residents with different age groups and dietary habits. Elevated levels of ∑PFASs were found nearby the FIP ranging from 79.9 ng/g to 200 ng/g in soils and from 58.8 ng/g to 8085 ng/g in crops. Perfluorooctanoic acid (PFOA) was the predominant PFAS component in soil; while shorter-chain perfluoroalkyl carboxylic acids (PFCAs), especially perfluorobutanoic acid (PFBA), were the major PFAS contaminants in multiple crops, resulting from their bioaccumulation preference. Depending on the crop types, the bioaccumulation factors (BAFs) of ∑PFASs for edible parts varied from 0.36 to 48.0, and the highest values were found in shoot vegetables compared with those in fruit vegetables, flower vegetables, root vegetables and grain crops. For typical grains, the BAFs of ∑PFASs decreased in the order of soybean (Glycine max (Linn.) Merr.), wheat (Triticum aestivum L.) and corn (Zea mays L.), possibly related to their protein and lipid content. Among specific organs in the whole plants, leaves exhibited the highest BAFs of ∑PFASs compared with corresponding roots, stems, husks or grains. With increasing carbon chain lengths of individual PFCAs (C4-C8), the logarithm of their BAFs for edible parts of various crops showed a linear decrease (0.1–1.16 log decrease per CF 2 unit), and the largest decrease was observed in grains. Human exposure to PFOA via the consumption of contaminated crops represents a health risk for local residents, especially for low-age consumers or urban consumers wit

Aim Climate change is having far-reaching effects on the global environment. Here, the ALARM (Assessing Large-scale Risks for Biodiversity with Tested Methods, European Union 6th Framework Programme) climate change scenarios were used to assess changes to the fate of selected persistent organic pollutants (POPs). Scenarios detailing climate and land-cover changes, such as precipitation, temperature and vegetation cover, were used as input in a European multi-media chemical fate model to help understand their impact on the environmental fate and behaviour of POPs over the period 1990–2100 in Europe.Location Europe.Methods Chemicals chosen for study included four classical POPs (two polychlorinated biphenyl congeners and two polybrominated diphenyl ether congeners). Using 30-year time steps, the model was run in steady-state mode four times for each chemical and each ALARM scenario.Results PCB153 displayed the greatest changes, with a reduction in burden of up to 40% in some Mediterranean compartments (e.g. soil and fresh water) under the worst case climate change scenario. The overall continental persistence of PCB153 was reduced by 1.5 years (12%) due to increased volatilization and degradation in air from a drier and warmer south-western Europe. This predicted loss resulted in a transfer and redeposition to the cooler and wetter north-eastern Europe, and increased the burden of PCB153 to Arctic compartments by up to 22%. The remaining chemicals displayed less pronounced changes, particularly under more the sustainable scenarios.Main conclusions Overall, the model simulations suggest that the dominant driver behind differences seen between the present and climate-changed future scenarios is temperature, resulting in a slight shift in chemical distribution from surface compartments to the air. This subsequently leads to a reduced continental persistence for PCBs and a north-easterly migration due to prevailing meteorological conditions. As a result of these calc

Air samples were taken for the analysis of persistent organic pollutants before, during, and after the national U.K. “Bonfire Festival” in November 2000. As expected, ambient levels of polynuclear aromatic hydrocarbons (PAHs) increased sharply in response to the widespread diffusive combustion processes that occurred at the time. Polybrominated diphenyl ethers (PBDEs) also increased at the suburban sampling location, to a greater extent than the PAHs. The rise and fall in PBDE concentrations was rapid, coinciding closely with the PAH “combustion markers”. These data provide evidence for a novel mechanism responsible for dissipation of PBDEs into the environment. It is hypothesized that products treated with the penta-BDE productnotably household furnishing foams and textileshave been subject to (unsanctioned) burning on private bonfires; even if the majority of the PBDE burden of such products is debrominated/broken down in the fires, it is shown that only small amounts of the total “stock” of penta product need be emitted to generate the concentra tions detected. The mixture of PBDEs in the air during the Bonfire Festival was enriched in higher brominated congeners (e.g., BDE-99, -153, and -154) compared to that in background air. Estimates are made of the masses of compound classes that may have been emitted to the atmosphere during the festival.