No abstract

Steroid estrogens at sub-micrograms per liter levels are frequently detected in surface water, and increasingly cause public concern of their potential impacts on ecosystems and human health. Assessing the environmental fate and risks of steroid estrogens requires accurate characterization of various physicochemical and biological processes involving these chemicals in aquatic systems. This paper reports sorption of three estrogens, 17beta-estradiol (estradiol), estrone, and 17alpha-ethinyl estradiol (EE2), by seven soil and sediment samples at both equilibrium and rate-limiting conditions. The results indicated that attainment of sorption equilibrium needs about 2 d when aqueous estrogen concentrations (C(t)s) are 25 to 50% of their solubility limits (S(W)S), but equilibrium requires 10 to 14 d when the Ct is 20 times lower than the S(W). The measured sorption isotherms are all nonlinear, with the Freundlich model parameter n ranging from 0.475 to 0.893. The observed isotherm nonlinearity correlates to a gradual increase of single-point organic carbon-normalized sorption distribution coefficient (capacity) (K(OC)) as the equilibrium estrogen concentration (Ce) decreases. At Ce = 0.5S(W), all three estrogens have log K(OC) values of 3.14 to 3.49, whereas at Ce = 0.02S(W), the log K(OC) values for estrone, EE2, and estradiol are within ranges of 3.40 to 3.81, 3.45 to 3.85, and 3.71 to 4.12, respectively. This study suggests that, when at sub-micrograms per liter levels, these estrogenic chemicals may exhibit even slower rates and greater capacities of sorption by soils and sediments.

Previous studies have reported high serum concentrations of polybrominated diphenyl ethers in residents of an electronic waste (e-waste) dismantling site in Guiyu town, South China. In this study, serum levels of Dechlorane Plus (DP), a chlorinated flame retardant of growing concern, were measured in residents of this region, and compared to those of a matched cohort from a nearby region in Haojiang, where fishing is the dominant industry. DP was detected in all the serum samples, with concentrations ranging from 7.8 to 465 ng/g lipid (median: 42.6 ng/g) and 0.93 to 50.5 ng/g lipid (median: 13.7 ng/g) in Guiyu and Haojiang, respectively. The Pearson's correlation coefficient between DP and decabromodiphenyl ether showed a positive relationship in Guiyu (r = 0.931, p < 0.01), but no correlation in Haojiang (r = 0.321, p = 0.34). The average anti-DP fractional abundances (f(anti) ratio) were 0.58 +/- 0.11 and 0.64 +/- 0.05 for Guiyu and Haojiang, respectively (p < 0.01). Tentatively identified dechlorination product ([-Cl + H]) was found in 19/40 serum samples (11/20 for Guiyu, 8/20 for Haojiang). These results suggest that the Guiyu and Haojiang cohorts experienced different dominant exposure routes. It is also possible that DP could bioaccumulate in a stereoselective manner, and undergo dechlorination metabolism. To the best of our knowledge, this is the first study to report DP levels in human serum. Further studies are needed to confirm the results of this study.

Abstract-The concentrations and distribution of seven organophosphate flame retardants and plasticizers (OPs) were investigated in 28 sediment samples collected from Taihu Lake. The analytes were ultrasonically extracted, enriched using solid-phase extraction, and determined by gas chromatography-mass spectrometry. The results indicated that the analytes were all detected in the sediments. The total concentrations of seven OPs ranged from 3.38 to 14.25 mg/kg, and tris (2-chloroiso-propyl) phosphate (TCPP), tris (2-chloroethyl) phosphate (TCEP), and tris (2-butoxyethyl) phosphate (TBEP) were the dominant compounds, with concentrations ranging from < limit of quantification to 2.27 mg/kg, 0.62 to 3.17 mg/kg, and 1.03 to 5.00 mg/kg, respectively. The highest concentration of total assessed OPs (14.25 mg/kg) was found at GH-5, with tris (1,3-dichloro-2-propyl) phosphate (TDCPP) as the main component at the sampling site. This result implied that there is an obvious emission source nearby at Suzhou City; in addition, human activities also play an important role in the concentration of OPs in the sediment.

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Aims:  Antibiotics from Bacillus subtilis JA show strong pathogen inhibition ability, which has potential market application; yet, the composition of these antibiotics has not been elucidated. The aim of this paper is to isolate and identify these antibiotics. Methods and Results:  The antagonistic activity of JA was tested in vitro; it exhibited strong inhibition against some important phytopathogens and postharvest pathogens. Crude antibiotic production was extracted with methanol from the precipitate by adding 6 mol l−1 HCl to the bacillus‐free culture broth. The crude extract was run on Diamonsil C18 column (5 μm, 250 × 4·6 mm) in HPLC system to separate the antibiotics. Major antibiotics were classified into three lipopeptide families according to electrospray ionization–mass spectrometry analysis. Subsequently, the classification of antibiotics was confirmed with typical collision‐induced dissociation fragments. Conclusions:  Three kinds of antibiotics were isolated from B. subtilis JA and were identified to the lipopeptide families, surfactin, iturin and fengycin. These compounds could function as biocontrol agents against a large spectrum of pathogens. Significance and Impact of the Study:  This study provided a reliable and rapid method for isolation and structural characterization of lipopeptide antibiotics from B. subtilis.

In this study, we recruited 49 subjects from one village close to an electronic waste (e-waste) site (exposed group) and another located 50 km away from the e-waste site (control group). We found that serum levels of polybrominated diphenyl ethers (median PBDEs, 382 ng/g lipid weight; range, 77-8452 ng/g lipid weight) and thyroid-stimulating hormone (median TSH, 1.79 microIU/mL; range, 0.38-9.03 microIU/mL) and frequencies of micro-nucleated binucleated cells (MNed BNC; median, 5% per hundred; range, 0-96% per hundred) were significantly higher in the exposed group than in the control group (158 ng/g, range of 18-436 ng/g, and p < 0.05; 1.15 microIU/mL, range of 0.48-2.09, and p < 0.01; and 0% per hundred, range of 0-5% per hundred, and p < 0.01, respectively). A history of working with e-waste was significantly associated with increased MNed BNC frequencies (odds ratio (OR), 38.85; 95% confidence interval (CI) = 1-1358.71, p = 0.044), independent of years of local residence, a perceived risk factor. However, there was no association between PBDEs exposure and oxidative DNA damage. Therefore, the exposure to PBDEs at the e-waste site may have an effect on the levels of TSH and genetoxic damage among these workers, but this needs to be validated in large studies.

FS-LASIK demonstrated a greater increase in PCE than SMILE only at 12 months, as well as a greater reduction of CRF than SMILE. There were no significant differences in PCE change over time within either group.