Insights into the release of triclosan from microplastics in aquatic environment assessed with diffusive gradient in thin-films.

Organic chemicals associated with microplastics (MPs) can be released and thus pose potential risks during weathering processes. However, the thermodynamics and kinetics of their release processes still need to be better understood. Herein, the adsorption and desorption kinetics of triclosan on polystyrene (PS) and polyvinyl chloride (PVC) were investigated by using both batch experiments and diffusive gradients in thin-films (DGT) technique. The pseudo-second-order model fitted the data best, implying that both intraparticle diffusion and external liquid film diffusion influence the adsorption and desorption processes. DGT continuously accumulated triclosan from MP suspensions but slower than theoretical values, indicating some restrictions to desorption. The DGT-induced fluxes in Soils/Sediment (DIFS) model, employed to interpret DGT data, gave distribution coefficients for labile species (Kdl) of 5000 mL g-1 (PS) and 1000 mL g-1 (PVC) and the corresponding response times (Tc) were 10 s and 1000 s, respectively. Higher Kdl but smaller Tc for PS than PVC showed that more triclosan adsorbed on PS could be rapidly released, while there were some kinetic limitations for triclosan on PVC. A novel finding was that pH and ionic strength individually and interactively affected the supply of triclosan to DGT. This is the first study to quantify interactions of organics with MPs by using DGT, aiding our understanding of MPs' adsorption/desorption behavior in the aquatic environment.

Mariculture affects antibiotic resistome and microbiome in the coastal environment.

Antibiotics are increasingly used and released into the marine environment due to the rapid development of mariculture, resulting in spread of antibiotic resistance. The pollution, distribution, and characteristics of antibiotics, antibiotic resistance genes (ARGs) and microbiomes have been investigated in this study. Results showed that 20 antibiotics were detected in Chinese coastal environment, with predominance of erythromycin-H2O, enrofloxacin and oxytetracycline. In coastal mariculture sites, antibiotic concentrations were significantly higher than in control sites, and more types of antibiotics were detected in the South than in the North of China. Residues of enrofloxacin, ciprofloxacin and sulfadiazine posed high resistance selection risks. ß-Lactam, multi-drug and tetracycline resistance genes were frequently detected with significantly higher abundance in the mariculture sites. Of the 262 detected ARGs, 10, 26, and 19 were ranked as high-risk, current-risk, future-risk, respectively. The main bacterial phyla were Proteobacteria and Bacteroidetes, of which 25 genera were zoonotic pathogens, with Arcobacter and Vibrio in particular ranking in the top10. Opportunistic pathogens were more widely distributed in the northern mariculture sites. Phyla of Proteobacteria and Bacteroidetes were the potential hosts of high-risk ARGs, while the conditional pathogens were associated with future-risk ARGs, indicating a potential threat to human health.

Influence of microplastics on triclosan bioaccumulation and metabolomics variation in Tilapia fish tissues.

Microplastics (MPs) and chemical pollutants usually coexist in aquatic environments. The bioaccumulation and metabolism of pollutants in aquatic organisms can be influenced by MPs. In this study, the bioaccumulation of triclosan (TCS) in tilapia tissues was determined, and metabolomics in the liver, gills, and gut were investigated after 10-day exposure to micro-sized polystyrene (PS) and TCS in water. The results showed that TCS bioaccumulated in various tissues, with the highest average concentration of 2728 ± 577 ng g-1 in the gut. The log bioaccumulation factors (BAFs) for TCS in these tissues were in the range of 0.99-3.56. Compared to the TCS treatment alone, MPs showed enhancement on the bioaccumulation of TCS in tilapia skin, liver, gut, gills, and stomach tissues in the TCS plus MP exposure. Especially in the skin and liver, the TCS concentrations were up to 2.06 and 1.38 times higher in the co-exposure of TCS and MPs, respectively. Based on the metabolomic analysis, MPs mainly disturbed the lipid and energy metabolism in tilapia fish. The altered metabolites between treatment with TCS alone and TCS + MPs were consistent, indicating that TCS has stronger disturbance in lipid and energy metabolism than MPs. This implies that the metabolism influence by the mixture of MPs and compounds is complicated in fish tissues.

Occurrence, mass loads and risks of bisphenol analogues in the Pearl River Delta region, South China: Urban rainfall runoff as a potential source for receiving rivers.

Bisphenol (BP) analogues are widely used as industrial materials and various product additives and are inevitably released into environment. However, knowledge on the sources of different BPs, especially those from urban rainfall runoff to the receiving rivers is very limited. In this study, 15 BPs were determined in surface water, sediments, wastewater treatment plant (WWTP) and rainfall runoff samples in the Pearl River region, South China. Eleven BPs were detected in surface water and sediments of the Pearl Rivers. BPA was the dominant compound up to 2080 ng/L in surface and 1970 ng/g in sediments, followed by BPF, BPS, BPTMC and BPAF. In WWTPs, 10, 9 and 8 BPs were detected in influents, effluents and excess sludges, respectively, with total BPs (ΣBPs) concentrations in effluents still at thousands ng/L, suggesting incompletely removal of BPs. Five BPs were detected in urban rainfall runoff samples, with the ΣBPs concentrations up to 7740 ng/L. Mass loads of ΣBPs from the rainfall runoff (5800 kg/y) were almost equivalent to the source from WWTPs (7370 kg/y) in the region, implying that the urban rainfall runoff was a potential source for BPs into the receiving river. The calculated estrogenic activity contributed by BPs showed low to median risks in sources and receiving rivers. But BPs are always as mixtures with other potential endocrine disrupting chemicals (EDCs) which probably pose high estrogenic activity risks. Hence, effective measures should be taken to decrease the input of EDCs from sources to receiving rivers.

Occurrence and mass loads of biocides in plastic debris from the Pearl River system, South China.

Chemical pollution in the plastic debris is an increasing global concern as most pollutants might transfer from the environment to living organisms via plastic debris. In this study, biocides in the plastic debris floating on the surface water of the Pearl River system were investigated. The abundances of large plastic debris and microplastics in the surface water were 0.07 ± 0.13 and 0.94 ± 1.87 items/m3, respectively. Totally, 15 and 16 out of 19 biocides were detected in the large plastic debris and microplastics, with the concentration of each biocide in the ranges of 22.6-2460 ng/g and 16.9-2890 ng/g, respectively. Meanwhile, the concentration ranges of the detected biocides were 0.01-215 ng/L in surface water. Triclosan, triclocarban, methylparaben, and N,N-diethyl-3-methylbenzamide (DEET) were the frequently detected compounds in the plastic samples and surface water. The partition coefficients (Kd) of biocides between the plastic debris and surface water showed a weak positive correlation with Kow values. Biocides were also detected on the natural floats (tree leaves and branches) at concentrations of 13.7-786 ng/g. The annual mass load of biocides in plastic debris at each site was up to 265 g/y, thereby suggesting that plastic debris might be an important carrier for the emerging contaminants, such as biocides.

Bioaccumulation and risks of 24 personal care products in plasma of wild fish from the Yangtze River, China.

We used a hybrid precipitation method to simultaneously extract and analyze 24 personal care products (PCPs), including 16 biocides, 4 synthetic musks, and 4 benzotriazoles, in the plasma of fish. The method's performance was validated for plasma samples with and without ß-glucuronidase/aryl-sulfatase hydrolysis. The recoveries were in the range of 70-120% for most of the PCPs, except N,N-diethyl-3-methylbenzamide (DEET), clotrimazole (CTZ), miconazole and itraconazole at spiking concentration of 20 and 5 ng/mL. The quantification limits ranged between 0.89 and 17.9 ng/mL (hydrolyzed plasma) and 0.85-18.5 ng/mL (non-hydrolyzed plasma), except CTZ at 77.5 ng/mL and 76.3 ng/mL. Totally, 13 PCPs were detected in plasma samples of fish collected from the Yangtze River, with a maximum concentration of 58.4 ng/mL (galaxolide). Compounds with the phenol hydroxyl groups of parabens or triclosan in hydrolyzed plasma showed higher concentrations than those in unhydrolyzed plasma with the ratio of conjugation (glucuronides + sulfates) forms up to 86%. The median values for the logarithm of bioaccumulation factors were between 1.39 and 4.15, which were 2-3 orders of magnitude higher than the theoretical logarithm of bioconcentration factors. Using the fish plasma model, the effect ratios (effect concentration/measured plasma concentration ratios) of tonalide, galaxolide, benzotriazole, triclosan, and DEET reached 0.35, 4.15, 3.78, 7.52, and 9.24, respectively. These are recognized as priority chemicals for further risk assessment.