Association of serum bisphenols, parabens, and triclosan concentrations with Sjögren Syndrome in the Hangzhou, China population.

Exposure to endocrine-disrupting chemicals (EDCs) has been linked to various immune deficiency disorders, including autoimmune diseases like Sjögren Syndrome (SjS). However, the detrimental effects of exposure to EDCs, including bisphenols, parabens, and triclosan (TCS), on SjS have been inadequately documented. Thus, we conducted a cross-sectional study that included both healthy individuals (controls) and patients with SjS (cases). We assessed serum concentrations of bisphenol A (BPA), bisphenol S (BPS), methyl parabens (MeP), ethyl parabens (EtP), and TCS. The relationship between the five EDCs levels and the risk of SjS was also explored. Additionally, we conducted an in-depth analysis of the collective influence of these EDCs mixtures on SjS, employing a weighted quantile sum regression model. Out of the five EDCs analyzed, EtP displayed the highest mean concentration (2.80 ng/mL), followed by BPA (2.66 ng/mL) and MeP (1.99 ng/mL), with TCS registering the lowest level (0.36 ng/mL). Notably, BPS exposure was significantly positively associated with the risk of being diagnosed with SjS (with an odds ratio [OR] of 1.17, p = 0.042). No statistically significant associations with SjS were observed for BPA, MeP, EtP, and TCS (p > 0.05). And we did not observe any significant effects of the EDCs mixture on SjS. To the best of our knowledge, this study is the first to suggest that BPS may potentially increase the risk of SjS. Although no significant effects were observed between other EDCs and SjS risk, we cannot disregard the potential harm of EDCs due to their non-monotonic dose response.

Spatial distribution characteristics of perfluoroalkyl substances in bulk and grain size fractionated sediments in Shenzhen Bay.

Understanding Perfluoroalkyl substances (PFASs) spatial distribution in natural environments is crucial due to their environmental persistence and potential bioaccumulation. However, limited research has investigated PFASs spatial distribution at a high resolution, especially in the Guangdong-Hong Kong-Macao Greater Bay Area. Here, we examined the composition and concentration of PFASs in 36 bulk surface sediments and grain-size fractionated sediments from 9 representative sites to determine the spatial distribution characteristics in Shenzhen Bay. We found that ΣPFASs decreased gradually from nearshore area to offshore area (0.680 and 0.297 ng g-1 dw, respectively). Furthermore, PFASs are easily adsorbed on fine-grained sediments, likely due to their chain length and hydrophobicity. We argue that the lateral movement of sediments may transport fine-grained sediments associated with ΣPFASs out of the bay, resulting in the spatial difference in ΣPFASs in Shenzhen Bay. Our findings provide important insights into explore the mechanisms associated with preservation and transport of PFASs.

GSH-Triggered/Photothermal-Enhanced H2S Signaling Molecule Release for Gas Therapy.

Traditional treatment methods for tumors are inefficient and have severe side effects. At present, new therapeutic methods such as phototherapy, chemodynamic therapy, and gasodynamic therapy have been innovatively developed. High concentrations of hydrogen sulfide (H2S) gas exhibit cancer-suppressive effects. Herein, a Prussian blue-loaded tetra-sulfide modified dendritic mesoporous organosilica (PB@DMOS) was rationally constructed with glutathione (GSH)-triggered/photothermal-enhanced H2S signaling molecule release properties for gas therapy. The as-synthesized nanoplatform confined PB nanoparticles in the mesoporous structure of organosilica silica due to electrostatic adsorption. In the case of a GSH overexpressed tumor microenvironment, H2S gas was controllably released. And the temperature increases due to the photothermal effects of PB nanoparticles, further enhancing H2S release. At the same time, PB nanoparticles with excellent hydrogen peroxide catalytic performance also amplified the efficiency of tumor therapy. Thus, a collective nanoplatform with gas therapy/photothermal therapy/catalytic therapy functionalities shows potential promise in terms of efficient tumor therapy.

Temporal variation of per- and polyfluoroalkyl substances (PFASs) abundances in Shenzhen Bay sediments over past 65 years.

We examined the vertical distribution of per- and polyfluoroalkyl substances (PFASs) and total organic carbon in sediment cores located in Shenzhen Bay area. We investigated the 210Pbex specific activity of the sediments and calculated the flux of PFASs to understand the temporal variation of PFASs in the past 65 years. The results showed that the concentrations of PFASs generally decreased with depth, ranging from 13 to 251 pg/g dw. The highest PFASs detected were perfluorobutanesulfonic acid, perfluorooctanoic acid, and perfluorohexanoic acid, which correspond to raw materials used in fire-fighting foam and food packaging industries. The flux of PFASs in Shenzhen Bay showed varying growth after 1978 when China's GDP entered a rapid growth stage. Our findings suggest that the vertical distribution of PFASs in Shenzhen Bay is fluctuating with the changes in industrial types and economic development, with implications for studying the fate of other persistent pollutants in the oceans.

Organophosphate esters concentrations in human serum and their associations with Sjögren syndrome.

Organophosphate esters (OPEs) are widely used as flame retardants and plasticizers due to their excellent properties. The interference of OPEs on immune function has been proven, but the epidemiological data on OPEs exposure to related immune function diseases, such as sjögren syndrome (SjS), is limited. In cross-sectional study, 283 serum samples were collected from healthy individuals (n = 145) and patients with SjS (n = 138) in Hangzhou, China. Eight OPEs, triethyl phosphate (TEP), tributyl phosphate (TBP), tris (2-chloroethyl) phosphine (TCEP), triphenyl phosphate (TPHP), tri (1-chloro-2-propyl) phosphate (TCIPP), 2-ethylhexyldi-phenyl phosphate (EHDPP), tris (1,3-dichloro-2-propyl) phosphate (TDCIPP), and tri (2-butoxyethyl) phosphate (TBOEP), were frequently measured in serum samples. In addition, we explored the associations between the serum OPEs concentration and the risk of SjS. Results showed that TEP (mean controls 2.17 and cases 3.63 ng/mL) was the most abundant OPEs in the serum samples of the control and case groups, followed by TCIPP (mean controls 0.54 and cases 0.78 ng/mL). Serum TEP, TPHP, and EHDPP concentrations were positively correlated with SjS [odds ratio (OR): 1.97, 1.96, and 2.42, respectively; 95% confidence interval (CI):1.34-2.89, 1.34-2.87, and 1.34-2.87, respectively] in the adjusted model, and a negative correlation of TBP concentrations with SjS in the adjusted model (OR: 0.35, 95% CI: 0.17-0.70) was observed. Compared with the lowest quartile concentrations, the ORs of SjS at the highest quartile concentrations of TEP (OR: 4.93, 95% CI: 2.24-10.82) and TPHP (OR: 4.75, 95% CI:1.89-11.94) were significantly higher. This study suggests that human exposure to OPEs may increase the risk of SjS.

Distribution and pollution characteristics of organophosphate esters: reflected by tree rings of arbor species.

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.

[Pollution Characteristics and Source Apportionment of Typical and Emerging Per- and Polyfluoroalkylated Substances in Tuojiang River Basin].

Forty-eight surface water samples were analyzed using ultra-performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) in order to study the pollution characteristics and source apportionment of per- and polyfluoroalkylated substances (PFASs) in the Tuojiang River. The results showed that ΣPFASs in the Tuojiang River ranged from 12.5-3789 ng·L-1, and perfluorooctanoic acid (PFOA) was the predominant PFAS, with a concentration of 9.97-3764 ng·L-1 (73.6%-99.8%), suggesting that legacy PFASs were still the dominant PFASs in the Tuojiang River. The most frequently detected emerging PFASs was 9-chlorohexadecafluoro-3-oxanonane-1-sulfonate (F-53B), with a detection frequency of 100%, suggesting the wide use of F-53B in the Tuojiang River. Sodium 1H, 1H, 2H, 2H-perfluorooctane sulfonate (6:2 FTS) displayed the highest concentration among all emerging PFASs[nd-27.3 ng·L-1, mean:(9.12±7.70) ng·L-1], and the concentrations were at the higher levels compared to those in other rivers around the world. In addition, ΣPFASs showed the highest concentrations of ΣPFASs at the fluorochemical manufacturing park (FMP), followed by those in the Luzhou section (in the lower reaches of the Tuojiang River), indicating that the emission of FMP and human daily production activities were the main influencing factors of PFASs pollution in the Tuojiang River. The estimated flux of PFASs from the Tuojiang River to the Yangtze River was 353 kg·a-1, and PFOA displayed the greatest mass loading (348 kg·a-1), which could provide the basic data for controlling PFASs in the Tuojiang River.

[Distribution Characteristics and Source Apportionment of Perfluoroalkyl Substances in Surface Soils of the Northeast Tibetan Plateau].

Surface soil samples collected at 18 sites from the northeast Tibetan Plateau were used to analyze perfluoroalkyl substances (PFASs) via ultra-performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) to study the concentration levels and sources of PFASs. The results showed that 11 PFASs were detected in the soil, and the ω(Σ11PFASs) ranged from 0.043-1.573 ng·g-1 with an average concentration of 0.398 ng·g-1. PFBA displayed the highest concentration level with a mean content of 0.164 ng·g-1, whereas PFHxA was at the lowest level (0.005 ng·g-1). The concentrations of the other PFASs were similar to each other (0.011-0.057 ng·g-1). Generally, PFASs contents in the west and north were higher than that in the southeast, and the alpine condensation effect existed for PFBA. The principal component analysis showed that PFASs in surface soils in the northeast Tibetan Plateau region mainly originated from the atmospheric transport of PFASs and their precursors. Few areas were affected by direct emissions of point source pollution, and the main sources were the industrial production of metals/minerals and other human activities.

Pollution characteristics and emissions of typical organophosphate esters of a wastewater treatment plant.

Effluent from wastewater treatment plants (WWTP) is an important source of organophosphate esters (OPEs) in the receiving rivers. In this paper, the concentration and distribution of seven OPEs in the water samples were determined, and the discharge was estimated. The results showed that the total removal rate of Σ7OPEs in water phase in WWTP was 57.2%. The average concentrations of Σ7OPEs in influent and effluent of the WWTP during rainy period were 3956.1 ± 1897.3 ng/L and 1461.9 ± 846.3 ng/L, respectively, which were about 4 times larger than those in influent water (978.2 ± 166.5 ng/L) and effluent (418.3 ± 12.0 ng/L) during non-rainy period, indicating that rainfall has a marked impact on the load of OPEs in WWTP and the receiving water. It was estimated that the average daily discharge of Σ7OPEs in the effluent of WWTP was 157.9 g, and the daily per capita contribution of the population in the area to the OPEs in the influent was 0.414 mg. During the shift of labour-intensive manufacturing from the coastal developed areas to inland regions, OPEs were widely used and produced in Southwest China. The total amount of OPEs emissions and its control should be taken into consideration.

Levels and Distribution of Organophosphate Esters (OPEs) in Typical Megacity Wetland Park Landscape Water Bodies in Southwest China.

Human activities have led to the release of organophosphate esters (OPEs) into the environment. This study aims to investigate the levels and partitioning of OPEs in surface water, suspended particulate matter (SPM) and sediments of landscape waters across eleven parks in the city of Chengdu, a megacity in Southwest China. The average concentration of Σ6OPEs in the SPM samples (median: 2.94 × 103 ng/L, 6.88 × 104 ng/g dry weight) was 1-3 orders of magnitude higher than that in the surface water (median: 359 ng/L) and sediment (median: 82.8 ng/g) samples. Tri-n-butyl phosphate (TnBP), tris-(2-chloroethyl)-phosphate (TCEP) and trichloropropyl phosphate (TCIPP) were the primary OPE pollutants in the surface water and SPM samples, while TnBP, tris-(2-butoxyethyl) phosphate (TBEP) and tris-(2-ethylhexyl) phosphate (TEHP) predominated the sediment samples. The higher log Koc values of OPEs in park landscape water bodies estimated in the present study relative to previous studies could be explained by the environmental conditions, such as the sources of the inputs and the hydraulic retention times in these surface waters.

Effects of Bisphenol A and Bisphenol S Exposure at Low Doses on the Metabolome of Adolescent Male Sprague-Dawley Rats.

Toxic effects induced upon exposure to low-dose bisphenol A (BPA) or bisphenol S (BPS) remains controversial. In this study, metabolomics was used to examine the metabolomic perturbation arising from 28 days of exposure to BPA or BPS at 50 µg/kg bw/day in Sprague-Dawley (SD) rats. Endogenous metabolite profiling revealed a clear discrimination of metabolome in the rat plasma among BPA-treatment, BPS-treatment, and control groups. BPA exposure induced the up-regulation of 19 metabolites and down-regulation of 32 metabolites in plasma of SD rats, compared with the control. BPS exposure induced the up-regulation of 15 metabolites and the down-regulation of 33 metabolites in the plasma of SD rats, compared with the control. Joint pathway analysis suggested marked perturbations in the citrate cycle, butanoate metabolism, and alanine, aspartate, and glutamate metabolism for BPA-exposed rats as well as glycerophospholipid metabolism for BPS-exposed rats. These findings provide novel insights into associations between the metabolomic perturbation and phenotypic changes arising from BPA and BPS exposure.

Performances of simultaneous enhanced removal of nitrogen and phosphorus via biological aerated filter with biochar as fillers under low dissolved oxygen for digested swine wastewater treatment.

This study aims to explore the feasibility of biochar as a carrier to improve the simultaneous removal of nitrogen and phosphorus in biological aerated filters (BAFs) for treating low C/N digested swine wastewater (DSW). Two similar BAFs (BAF-A with hydrophobic polypropylene resin as fillers and BAF-B with bamboo biochar as carrier) were developed for DSW treatment. Results showed that the NH4+-N, TN, and TP removal performances in BAF-B were higher than those in BAF-A. Carrier type had an obvious influence on the structures and diversity of the microbial population. The biochar carrier in BAF-B was conducive to the enrichment of the functional microorganisms and the increase of microbial diversity under high NH4+-N conditions. Microbial analysis showed that the genera Rhodanobacter (10.64%), JGI_0001001-h003 (14.24%), RBG-13-54-9 (8.87%), Chujaibacter (11.27%), and Ottowia were the predominant populations involved in nitrogen and phosphorus removal in the later stage of phase III in BAF-B. BAF with biochar as carrier was highly promising for TN and TP removal in low C/N and high NH4+-N DSW treatment.

Levels of per- and polyfluoroalkyl substances (PFAS) in ski wax products on the market in 2019 indicate no changes in formulation.

In the summer of 2019, eleven of the best-selling fluorinated ski wax products were purchased from one of Norway's largest sports stores and soon after analysed for a suite of 26 per- and polyfluoroalkyl substances (PFAS). The waxes were shown to contain a wide range of perfluoroalkyl acids, including perfluoroalkyl carboxylic acids with up to 25 carbons. Of particular concern was the finding that perfluorooctanoic acid (PFOA) levels in nine of the eleven ski lubrication products analysed were above the EU limit values of 25 ng g-1, which came into force on 4th July 2020. The ski wax with the highest PFOA levels had a concentration that was 1215 times higher than the EU restrictions. Although some of the ski wax manufacturers have indicated that they have switched to formulations that contain chemistries based on shorter perfluoroalkyl chains, the analytical results show that this is not the case.

Environment occurrence of perfluoroalkyl acids and associated human health risks near a major fluorochemical manufacturing park in southwest of China.

Despite China being the largest global manufacturer of perfluoroalkyl acids (PFAAs), few studies have been carried out on the environmental occurrence and associated human health risks of PFAAs emitted from manufacturing sites in China. Here, river water, tap water, soil and leaf samples were collected around a major fluorochemical manufacturing park (FMP) in the southwest of China in 2019. High ΣPFAA concentrations (sum of 12 PFAAs) of 3817 ng/L, 3254 ng/L, 322-476 ng/g dw and 23401-33749 ng/g dw were measured near the FMP in river water, tap water, soil and leaves, respectively, indicating that the FMP is a point source of PFAAs. PFOA was the predominant PFAA in all samples (58.5-98.6 %) indicating the production or use of PFOA at the FMP. PFOA concentrations in most tap water samples (> 300 ng/L in 31 of 38 samples) exceeded the U.S. EPA health advisory. Proportions of branched PFOA isomers in all samples were in 5.9-47.4 %, suggesting the production or use of PFOA manufactured by electrochemical fluorination at the FMP. It is recommended to focus more attention on branched PFOA isomers in the future because otherwise health risks may be underestimated due to their relatively high proportions in China.

Occurrence of phthalic acid esters in sediment samples from East China Sea.

Phthalic acid esters (PAEs) are widely used as plasticizers in many industrial and household products. The widespread distribution of PAEs in marine environment has attracted great concerns, due to their adverse health effects on marine organisms. However, the data on the occurrence of PAEs in sediment from East China Sea is still scarce. In this study, 16 PAEs were analyzed in 67 sediment samples collected from the Hangzhou Bay, Taizhou Bay, and Wenzhou Bay. Eight PAEs were detected in collected sediment samples, and the total concentrations of detected PAEs (∑PAEs) were in the range of 654-2603 ng/g. The di(2-ethylhexyl) phthalate (DEHP) was the predominant PAE (mean 663 ng/g; accounted for mean 52% of ∑PAEs), followed by di-isobutyl phthalate (DiBP; 284 ng/g; 22%), di-n-butyl phthalate (DBP; 184 ng/g; 15%), and dimethyl phthalate (63 ng/g; 5.0%). The mean sediment concentration of ∑PAEs in the Hangzhou Bay (1623 ng/g) was higher than that in the Taizhou Bay (1282 ng/g) and Wenzhou Bay (1185 ng/g). Concentrations of diethyl phthalate, DiBP, and DBP were significantly and positively correlated with one another in sediment from Taizhou Bay and Wenzhou Bay. The estimated inventories of ∑PAEs in sediment from Hangzhou Bay, Taizhou Bay, and Wenzhou Bay were 82 tons, 28 tons, and 26 tons, respectively. Overall, this study provides the first data on the occurrence of PAEs in sediment from the East China Sea, which is necessary to conduct the PAE exposure risk assessment for the marine benthos.

Occurrence of phthalic acid esters in marine organisms from Hangzhou Bay, China: Implications for human exposure.

Owing to the wide application of phthalic acid esters (PAEs) in the manufacturing of plastic products, they are ubiquitous in the marine environment. However, the occurrence of various PAEs in marine organisms from China has not been well characterized. In this study, 341 marine organism samples (including fish, shrimp, crab, and shellfish) were collected from Hangzhou Bay, China and analyzed for 16 PAEs. Further, the human PAE exposure risks raised from the consumption of marine organisms were evaluated for adults and children. In total, eight PAEs were detected in collected organism samples, with the concentration of total PAEs (∑PAEs) ranging from 64 to 2840 ng/g (mean 238 ng/g). Crab (mean 811 ng/g) samples had the highest mean concentration of ∑PAEs, followed by fish (465 ng/g), shrimp (293 ng/g), and shellfish (261 ng/g) samples. Among detected PAEs, di-isobutyl phthalate (DiBP), di-n-butyl phthalate (DBP), and di-ethylhexyl phthalate (DEHP) were the predominant PAEs, and they collectively accounted for 84-97% of the ∑PAEs concentrations in all samples. The estimated daily intakes of DiBP, DBP, and DEHP were more than one order of magnitude higher than remaining PAEs. Calculated hazard quotient values of PAEs were all <0.1, suggesting non-cancer risks for the general population through the consumption of marine organisms. Overall, for the first time, this study systematically examined the occurrence of multiple PAEs in four types of marine organisms from Hangzhou Bay, China.

[Pollution Characteristics and Exposure Risk Assessment of Perfluoroalkyl Substances in Road Dust, Chengdu].

To study the pollution characteristics and exposure health risk of perfluoroalkyl substances (PFASs) in road dust, 12 PFASs were analyzed by ultra-performance liquid chromatography tandem mass spectrometry (UPLC-MS/MS) in this study. PFAS concentrations in road dust ranged from 0.95 to 111 ng·g-1, with an average concentration of (25.6±37.2) ng·g-1, suggesting large spatial differences between PFASs in road dust. PFAS concentrations on the main roads were significantly higher than on minor roads, and the minor roads downtown displayed higher concentration levels than suburban minor roads. Perfluorobutanoic acid (PFBA) was the predominant compound in Section 1 of Jie-fang Road, Jin-niu-ba Road and Shui-nian-he Road, while perfluroroocantanoic acid (PFOA, 24.8%) and perfluorooctane sulfonate (PFOS, 24.1%) were the main PFASs on other roads, indicating different sources of PFASs in these areas. The total daily dose of PFASs in road dust for children and adults were 0.168 ng·(kg·d)-1 and 0.028 ng·(kg·d)-1, respectively, suggesting higher exposure risk for children than adults. Therefore, more attention should be paid to children's health risk assessment. Daily doses of PFOA and PFOS in road dust for Chengdu residents were lower than the maximum daily intakes recommended by the European Authority, indicating that there was no immediate health risk to local residents.

Spatiotemporal distribution and isomer profiles of perfluoroalkyl acids in airborne particulate matter in Chengdu City, China.

Airborne particulate matter (APM) was collected in four seasons at five different areas of the city of Chengdu, China to study the spatial and seasonal contamination pattern of perfluoroalkyl acids (PFAAs). The results showed that ∑PFAA concentrations in Downtown Chengdu (mean value: 297 ±â€¯238 pg/m3) were higher than concentrations in suburban areas. The highest concentrations of PFAAs occurred during spring (97.5-709 pg/L; arithmetic mean concentration: 297 ±â€¯191 pg/L) while the lowest concentration occurred during autumn (9.27-105 pg/L; arithmetic mean concentration 41.1 ±â€¯24.8 pg/L). Perfluorooctanoic acid (PFOA) was the main PFAA quantified during winter, summer and autumn, and perfluorononanoic acid (PFNA) was the predominant PFAA in spring. Relative humidity (RH) and average daily precipitation (PRE) showed significant negative correlations with PFAA concentrations in winter and summer, suggesting that they played an important role in controlling PFAA concentrations in APM. The linear structural isomer of PFOA (n-PFOA) was the most abundant isomer in APM in Chengdu, with the average proportion of 85.6% ±â€¯6.13%, higher than the proportion in ECF PFOA commercial products (74.3-77.6%). However, the consistent fingerprint of branched PFOA in the APM implies that ECF PFOA makes a significant contribution to the PFOA in APM. PFOS in the APM collected throughout the year had a mean proportion of 54.0 ±â€¯8.81% of n-PFOS. This proportion of n-PFOS is lower than commercial ECF products (62.9-78.2%), suggesting an additional proportion of branched PFOS isomers in APM in Chengdu.

Bioaccumulation of perfluoroalkyl acids including the isomers of perfluorooctane sulfonate in carp (Cyprinus carpio) in a sediment/water microcosm.

Carp (Cyprinus carpio) were exposed to perfluoroalkyl acids (PFAAs) including perfluorooctane sulfonate (PFOS) isomers in an artificially contaminated sediment/water microcosm. The uptake constant of PFAAs increased with increasing carbon chain length, whereas the elimination coefficient displayed the opposite trend, suggesting that carbon chain length plays an important role in the bioaccumulation of PFAAs. When the contribution of suspended particulate matter was taken into account, the bioaccumulation factors (BAFs) became lower (3.61-600 L/kg) compared with BAFs derived from only considering the absorption from free PFAAs in water (3.85-97000 L/kg). The results indicate that suspended particulate matter in water constitutes an important source of exposure for aquatic organisms to long-chain PFAAs. Linear (n-)PFOS was preferentially accumulated compared with branched isomers in carp. Among the branched isomers, 1m-PFOS displayed the greatest bioaccumulation, whereas m2 -PFOS had the lowest. Linear PFOS displayed greater partitioning ability from blood to other tissues over branched PFOS (br-PFOS) isomers, leading to a relatively lower n-PFOS proportion in blood. In summary, suspended particulate matter made a contribution to the accumulation of long-chain PFAAs in aquatic organisms, and n-PFOS was preferentially accumulated compared with br-PFOS isomers. Environ Toxicol Chem 2016;35:3005-3013. © 2016 SETAC.

Behaviors of N-ethyl perfluorooctane sulfonamide ethanol (N-EtFOSE) in a soil-earthworm system: Transformation and bioaccumulation.

N-ethyl perfluorooctane sulfonamido ethanol (N-EtFOSE) is a typical precursor of perfluorooctane sulfonate (PFOS). In this study, the behaviors of N-EtFOSE in a soil-earthworm system, including biodegradation in soil and bioaccumulation and biotransformation in earthworms (Eisenia fetida) were investigated. N-EtFOSE could be biodegraded in soil and biotransformed in earthworms to several metabolites, including n-ethylperfluorooctane sulfonamide acetate (N-EtFOSAA), perfluorooctane sulfonamide acetate (FOSAA), perfluorooctane sulfonamide (FOSA) and PFOS, with N-EtFOSAA as the predominant intermediate and PFOS as the terminal product in both soil and earthworm. The uptake rate coefficients (ku, 0.746 goc gdw(-1)d(-1)), degradation rate constant in soil (k0, 0.138 d(-1)) and the biota-to-soil accumulation factor (BSAF, 0.523 goc gdw(-1)) of N-EtFOSE were estimated. For N-EtFOSE, N-EtFOSAA, FOSAA, FOSA and PFOS, their loss rate constants in earthworms were in the range of 0.467-30.2 (α) and 0.006-0.415 (ß) d(-1), respectively. The results provided important information about the behaviors of N-EtFOSE in the soil-earthworm system.