Xialin Hu

Occurrence, distribution and seasonal variation of antibiotics in the Huangpu River, Shanghai, China

Water samples were collected from 19 sampling sites along the Huangpu River in June and December 2009. The occurrence, distribution and seasonal variation of 22 antibiotics, including four tetracyclines, three chloramphenicols, two macrolides, six fluoroquinolones, six sulfonamides and trimethoprim were investigated. It was found that all 19 sampling sites were contaminated by antibiotics. Four antibiotics (sulfamerazine, norfloxacin, fleroxacin and sarafloxacin) were not detected. The detection frequencies of the other 18 antibiotics were in the range of 5.3-100%. The median concentrations of the detected antibiotics ranged from quantification limits to 36.71 ng L(-1) (tetracycline) in June and to 313.44 ng L(-1) (sulfamethazine) in December. The number of detected antibiotics and the overall antibiotic concentrations were higher in December than in June due to the different river flow conditions. Different dominant antibiotics were observed for each group of antibiotics between June and December. Higher total concentrations of veterinary antibiotics such as tetracyclines were observed in suburban sampling sites than in urban sites, indicating the role of livestock and agricultural activities as an important source of antibiotic contamination.

Prevalence of antibiotic resistance genes and their relationship with antibiotics in the Huangpu River and the drinking water sources, Shanghai, China

The prevalence of antibiotic resistance genes (ARGs) and their relationship with antibiotics in the surface waters of the Huangpu River and the drinking water sources of Shanghai, China, were investigated. 39 ARGs, including four sulfonamide ARGs, 23 tetracycline ARGs, four chloramphenicol ARGs, five β-lactam ARGs and three penicillin ARGs were targeted in this study. Two sulfonamide ARGs (sul I and sul II), eight tetracycline ARGs (tet(A), tet(B), tet(C), tet(G), tet(M), tet(O), tet(W) and tet(X)), and one β-lactam ARG (TEM) were detected to be present in water samples by polymerase chain reaction (PCR), with the detection frequencies ranging from 42.86% to 100%. The average concentrations of the 11 ARGs ranged from 3.66×10(1) copy/mL (tet(B)) to 1.62×10(5) copy/mL (sul II), quantified by quantitative real-time PCR (QPCR). The number of detected ARGs and the ARG concentrations were generally higher in suburban sampling sites than in urban sites. Being in or near suburban rural areas, some raw drinking water sources were observed to have comparatively higher ARG contamination, drawing an urgent attention for the concern of public health. Generally consistent relations were observed between the concentrations of tet genes and the tetracycline levels and between the concentrations of sul genes and the sulfonamide levels.

Adsorption of cadmium(II) on humic acid coated titanium dioxide

The rapid increase in nanotechnology has led to growing concerns on environmental effects and health risks of nanoparticles (NPs). Many studies investigated the adsorption of toxic pollutants on NPs; however, the interaction between heavy metals and natural organic matter (NOM) coated metal oxide NPs was scarcely studied. In this study, using humic acid (HA) as model NOM, the adsorption of Cd(II) on humic acid coated titanium dioxide (HA-TiO(2)) NPs was investigated. Solution parameters such as pH and salinity were investigated to exploit the mechanisms. Our results demonstrated that the adsorption isotherms of Cd(II) to both TiO(2) and HA-TiO(2) complied well with Freundlich model. q(e) values increased with pH increase, mainly due to electrostatic attraction, whereas q(e) values increased initially and then decreased at 100 mmol L(-1) with salinity increase, mainly due to complexation and electrostatic effects. It is noteworthy that an overall trend of higher Cd(II) adsorption was observed on HA-TiO(2) compared to that on TiO(2), implying that HA coating might modify bioavailability of heavy metals in aquatic environment. The possible adsorption mechanisms in views of electrostatic interactions and covalent effects were interpreted, and the X-ray photoelectron spectroscopy (XPS) results also verified the possible mechanisms.

Combined effects of titanium dioxide and humic acid on the bioaccumulation of cadmium in Zebrafish.

The combined effects of titanium dioxide (TiO2) nanoparticles and humic acid (HA) on the bioaccumulation of cadmium (Cd) in Zebrafish were investigated. Experimental data on the equilibrium Cd bioaccumulation suggest that only the dissolved Cd effectively contributed to Cd bioaccumulation in HA solutions whereas both the dissolved and TiO2 associated Cd were accumulated in TiO2 or the mixture of HA and TiO2 solutions, due likely to the additional intestine uptake of the TiO2-bound Cd. The equilibrium Cd bioaccumulation in the mixed system was comparable to that in the corresponding HA solutions, and significantly lower than that in the corresponding TiO2 solutions (n=3, p<0.05). The presence of either HA or TiO2 (5-20 mg L(-1)) in water slightly increased the uptake rate constants of Cd bioaccumulation whereas combining HA and TiO2 reduced the uptake rate constants.

MCX based solid phase extraction combined with liquid chromatography tandem mass spectrometry for the simultaneous determination of 31 endocrine-disrupting compounds in surface water of Shanghai.

A novel analytical method employing MCX (mixed-mode cationic exchange) based solid phase extraction (SPE) coupled with liquid chromatography tandem mass spectrometry (LC-MS/MS) was developed to detect 31 endocrine-disrupting compounds (EDCs) in surface water samples simultaneously. The target EDCs belong to five classes, including seven estrogens, eight androgens, six progesterones, five adrenocortical hormones and five industrial compounds. In order to simultaneously concentrate the target EDCs and eliminate matrix interferences in the water samples, MCX SPE cartridges were employed for SPE, and then followed by a simple and highly efficient three-step sequential elution procedure. Two electrospray ionization (ESI) detection modes, positive (ESI+) and (ESI-), were optimized for HPLC-MS/MS analysis to obtain the highest sensitivity for all the EDCs. The limits of detection (LODs) were 0.02-1.9 ng L(-1), which are lower than or comparable to these reported in references. Wide linear ranges (LOD-100 ng L(-1) for ESI+ mode, and LOD-200 ng L(-1) for ESI- mode) were obtained with determination coefficients (R(2)) higher than 0.99 for all the compounds. With five internal standards, good recoveries (84.4-103.0%) of all the target compounds were obtained in selected surface water samples. The developed method was successfully applied to investigate the EDCs occurrence in the surface water of Shanghai by analyzing surface water samples from 11 sites. The results showed that nearly all the target compounds (30 in 31) were present in the surface water samples of Shanghai, of which three industrial compounds (4-t-OP, BPA, and BPF) showed the highest concentrations (median concentrations were 11.88-23.50 ng L(-1)), suggesting that industrial compounds were the dominating EDCs in the surface water of Shanghai, and much more attention should be paid on these compounds. Our present research demonstrated that SPE with MCX cartridges combined with HPLC-MS/MS was convenient, efficient and reliable for multiclass analysis of EDCs in surface water.

The effects of humic acid on the uptake and depuration of fullerene aqueous suspensions in two aquatic organisms

The authors investigated the uptake and depuration of fullerene aqueous suspensions (nC(60)) in 2 aquatic organisms: Daphnia magna and zebrafish. The effects of humic acid were examined to elucidate its possible mechanisms in the aquatic environment. The uptake was concentration-dependent in both organisms, and the maximum uptake concentration of nC(60) in Daphnia (2268 ± 158 mg/kg) was approximately 1 order of magnitude higher than that in zebrafish (222 ± 30 mg/kg) because of the larger gut volume ratio to the mass of Daphnia or its high uptake efficiency. Humic acid reduced the uptake of nC(60) in Daphnia and zebrafish as a result of the size effect and the polarity alternation of nC(60). The depuration patterns were rapid for Daphnia and slow for zebrafish, and the differences were most likely the result of different water exchange frequencies between organisms. The remaining nC(60) percentages were approximately 20% for Daphnia and 30% for zebrafish after 48-h depuration, suggesting that a large nC(60) burden still existed for both aquatic organisms and that there is a need for further studies on the potential for trophic transfer.

Simultaneous solid phase extraction coupled with liquid chromatography tandem mass spectrometry and gas chromatography tandem mass spectrometry for the highly sensitive determination of 15 endocrine disrupting chemicals in seafood.

This study aimed to develop a sensitive and reliable multi-residue method for the determination of trace amounts of endocrine disrupting chemicals including five phthalate esters (PAEs), five monoalky phthalate esters (MPEs), four alkylphenols (APs) and bisphenol A (BPA) in seafood. Ultrasonic liquid extraction was selected for extraction based on acetonitrile, instead of frequently-used n-hexane, due to its lower background of PAEs. Application of solid phase extraction (SPE) with primary secondary amine (PSA, 1g/6 mL) cartridge achieved the relatively low matrix effects for MPEs and BPA in seafood. To our knowledge, it is the first study reporting about simultaneous extraction and purification of PAEs, MPEs, APs and BPA in biota samples. To obtain the maximum sensitivity, both liquid chromatography tandem mass spectrometry (LC-MS/MS) and gas chromatography tandem mass spectrometry (GC-MS/MS) were applied for analysis. This method was validated and tested on fish, mollusk and prawn. Sufficient linearity was verified by Mandels fitting test for the matrix-matched calibrations used in this study for MPEs, APs and BPA, between 0.5 ng/g and 200 ng/g or 400 ng/g. And correlation coefficients of all calibrations suppressed 0.99 for all analytes. Good recoveries were obtained, ranging from 60% to 127% for most compounds. The sensitivity was good with method detection limits (MDLs) of 0.015-2.2 ng/g wet weight (ww) for all compounds. Most MDLs are much lower than those in previous reports. The sensitive method was then applied on real fish, mollusk and prawn samples from the Yangtze River Delta sea area (China), and all the target compounds were detected with the maximum concentrations of PAEs, MPEs, APs and BPA up to 219.3 ng/g ww, 51.4 ng/g ww, 62.0 ng/g ww and 8.6 ng/g ww, respectively.

Characteristics of the alkylphenol and bisphenol A distributions in marine organisms and implications for human health: A case study of the East China Sea.

The distributions of alkylphenol (AP) and bisphenol A (BPA) in marine organisms, including fish, prawns and molluscs, could reflect the exposure of AP and BPA directly and effectively. This paper provides the first report on the species-dependent distribution and the human health risks of four APs (4-t-octylphenol, 4-t-OP; 4-octylphenol, 4-OP;4-nonylphenol, 4-NP; 4-n-nonylphenol, 4-n-NP) and BPA in 95 wild and 88 processed marine biota samples from the East China Sea of the Yangtze River Delta area. 4-NP was the predominant compound with the highest detected concentration of 19,890.50ng/g ww. Significant pollution was observed in Taizhou, Shanghai and Ningbo. The species-dependent distribution was related to food habits, living patterns and trophic transfer. Higher residual concentrations of 4-t-OP, 4-OP, 4-n-NP and BPA were observed in fish species that consumed benthic organisms or demersal fish species, whereas 4-NP showed different results due to trophic dilution. The trophic magnification factors (TMFs) of the linear APs (4-OP and 4-n-NP) (1.22-2.93) were higher than those of the branched ones (4-t-OP and 4-NP) (0.72-0.90), indicating the relative metabolism stability of linear APs. 4-NP has the lowest TMF value of 0.72, and its trophic dilution might be observed because the branched carbon chain exhibits the lowest dispersion force compared to that of the other APs. As for the health risk, 7-year old children may be exposed to the highest health risk of 4-NP with 95th percentile values of the hazard quotient of 0.22 to 0.23; however, the risks of the other chemicals were relatively low.

Fullerene‐associated phenanthrene contributes to bioaccumulation but is not toxic to fish

The present study investigated the effects of aqueous fullerene suspensions (nC60 ) on the bioavailability and toxicity of phenanthrene (Phe) to junior carp (Cyprinus carpio). Bioaccumulation factors (BAFs) were calculated based on total as well as free concentrations of Phe. Equal BAF values were obtained with and without nC60 based on the total concentrations, whereas greater BAFs were found in the presence of nC60 when free Phe concentrations were applied. The results demonstrated that nC60 could act as a contaminant carrier to facilitate Phe bioaccumulation. The concentration-response relationship of induced hepatic 7-ethoxysorufin-O-deethylase activity was established in regard to the total and free concentrations of aqueous Phe solutions as well as the body residues. The concentration-response curves were reliant on the nC60 concentration when the total concentration of Phe was employed as a variable but were independent of nC60 presence when free concentration or body residue was employed as a variable, implying that the latter 2 parameters were more accurate in evaluating biological effects. Particles of C60 were mostly distributed in fish liver and intestines, which indicated the primary routine of uptake was through ingestion. Approximately 22% to 100% of the Phe-nC60 complex contributed to the bioaccumulation, whereas the complex did not contribute to the toxicity.

Combined effects of aqueous suspensions of fullerene and humic acid on the availability of polycyclic aromatic hydrocarbons: Evaluated with negligible depletion solid-phase microextraction

The wide application of engineered carbon nanomaterials, such as fullerene (C60), will inevitably result in their introduction into the aqueous environment. Interactions of C60 with abundant natural organic matter (NOM) will likely alter the bioavailability of organic compounds to aquatic organisms. The availability of 12 types of polycyclic aromatic hydrocarbons (PAHs) in various aqueous suspensions of fullerene (nC60) prepared by different methods, e.g., in humic acid (HA) and particularly in combined systems of nC(60) and HA, was investigated by negligible depletion solid-phase microextraction (nd-SPME). The results showed that HA accelerated the rate constants (k2) of almost all PAH uptakes to the nd-SPME fibers compared with the solutions without the matrix; the combined matrices of nC(60) and HA significantly promoted the k2 of highly hydrophobic PAHs (logKOW 5.81-6.20), whereas they retarded that of less hydrophobic ones (logKOW 3.82-4.63) (p<0.05). Remarkable or minor reduction of free concentration of PAH was observed in the combined system of nC(60) and HA depending on the properties of individual PAHs. Sorption coefficients (KHA, K(C60) and K(C60+HA)) of various PAHs in different matrices were provided, and matrix concentrations showed no significant effects. For highly hydrophobic PAHs (logKOW 5.16-6.20), the logK(C60+HA) >= logKHA > logK(C60), whereas for less hydrophobic PAHs (logKOW 3.8-4.63), the Kmatrix values in various matrices showed no noticeable trend. In addition, higher K(C60) values were obtained for aqu/nC(60) than for son/nC(60) for most highly hydrophobic PAHs. The above results suggest that hydrophobicity plays an important role in determining Kmatrix in addition to the matrix effects. The interactions between nC(60) and HA have critical or minor impacts on availability, and thus bioavailability, of PAHs. This paper contributes to the understanding of the bioavailability mechanisms of organic pollutants in the aquatic environment with both nC(60) and NOM.