Cross‐sectional epidemiological study on arsenic excretion in urine of children and workers in Greece

An investigation was undertaken to study the exposure of children in areas with different air pollution and of adults working in three different plants (lead processing, battery plant, oil refinery) using arsenic in urine as a biological parameter. The arsenic excretion of the children are in agreement with the air pollution in the investigated areas. The workers in the lead processing plant are found to have the highest urine excretion values of the three worker collectives. The mean excretion values is nearly ten times higher than that found in the normal population.     

The occurrence of disinfection by‐products in Taiwan drinking water

In this study, samples were taken from six conventional water treatment plants for disinfection by‐products analysis. Results from the analysis revealed that trihalomethanes (THMs) concentrations in all samples were below regulatory levels (100 μg/L). Although the national standard for haloacetic acids (HAA5) has not yet been promulgated in Taiwan, samples from two water plants contained HAA5 concentrations exceeding the USEPA limit (MCL of HAA5 of Stage 1, 60 μg/L). THMs and HAA5 were found to be the major disinfection by‐products in all water treatment plants. It was noted that the concentration of HAA5 in most samples was higher than that of the trihalomathanes. However, the formation potential of THM (THMFP) was found to be higher than that of HAA (HAAFP). Good correlation also was found between THMFP (or THMFP) and HAA5 (or THMs). In evaluating the performance of the treatment processes, it was found that conventional water treatment processes followed by activated carbon were effective in removing disinfection by‐products (DBPs) from source water with pre‐ozonation. The treatment processes were at their optimum performance in removing contaminants when O₃/TOC₀ was held at 0.75.     

Monitoring of drinking water treatment plants using ICP‐MS

More than sixty inorganic parameters were monitored in the Ter and Llobregat Drinking Water Treatment Plants (DWTPs) using ICP‐MS. Both DWTPs supply approximately four million inhabitants with water in Barcelona and neighbouring areas (NE Spain). The profile of inorganic parameters throughout the treatment process is similar in the Ter and Llobregat DWTPs. Sodium, K, Mg, Ca, Si, Cl^‐, SO₄ ^‐2, Li, Rb, Cs (only in the case of the Llobregat DWTP), Sr, Ba, B, Ti, Cr, V, Co, Ni, Zn, Cu, Sb, Mo, Pb and U were not removed from raw water. Consequently, no improvement was shown as regards the high salinity of Llobregat raw water which is related to the mining activities on the large salt deposits located in the upper part of the basin. However, P, Fe, Mn, Cu and As were removed during treatment. The results obtained reveal the suitability of ICP‐MS for inorganic water quality monitoring in DWTP.     

Presence of Cd‐binding proteins in pre‐exposed and not pre‐exposed cadmium brine shrimp Artemia

The presence of metal binding proteins has been variously suggested as indicating involvement in uptake, storage, transport and elimination of toxic metals and in the routine metabolism of metals in mammals and a variety of marine invertebrates. This report describes results on the characterization of Cd‐BPs obtained from cadmium pre‐exposed and not pre‐exposed Anemia. The effect of pre‐exposure in the Cd‐binding protein induction in Artemia is discussed.     

Effects of water velocity on bulk water quality and biofilm population structure in drinking water distribution systems北大核心CSCD

To study the effect of flow velocity on drinking water distribution systems, bulk water quality was monitored over 28 days, biomass was measured, and 16S rDNA was sequenced on the 28th day using a water distribution simulation system. The relationship between bulk water quality and biofilm was statistically analyzed. Flow velocity of 0.5 m/s yielded the most total organic carbon (TOC) (5.26 ± 0.17 mg/L) in the bulk water, the most bulk water bacteria (lg (n+1/mL-1) = 4.79 ± 0.02), the worst bulk water quality, and the most biofilm bacteria (lg (n+1/cm-2) = 5.48 ± 0.06). A Pearson correlation analysis showed the total number of biofilm bacteria was positively correlated with conductivity (R = 0.73, P < 0.01), turbidity (R = 0.87, P < 0.001), TOC (R = 0.94, P < 0.001), and total bacteria (R = 0.92, P < 0.001), and was negatively correlated with residual chlorine (R = -0.68, P < 0.05). Biofilm diversity was high under the low (0.1 m/s) and high (2.5 m/s) flow rates, but the bacterial diversity of biofilm was the lowest at the 0.5 m/s flow rate, in which Proteobacteria dominated the biofilm community structure. These results suggest that flow velocity affects bulk water quality and biofilm population structure, and water quality and biofilm population structure are interrelated, which provides the theoretical basis for research on biofilms in drinking water distribution systems. © 2018 Science Press. All rights reserved.     

Effect and its time lags of water level fluctuations in Three Gorges Reservoir on the macroinvertebrates in a tributary bay北大核心CSCD

In order to study how water level fluctuations (WLF) of reservoir influence the macroinvertebrate in tributary bay, we studied the effect of WLF of the Three Gorges Reservior on macroinvertebrate communities in Xiangxi Bay, and the time lags of such effect, based on the surveys in spring and summer from 2005 to 2010. In this research, WLF was represented by water level drawdown (WLD) and the sum of absolute values of rate of water level fluctuations (RWlf). Pearson correlation analysis was used to analyze the relationship between WLF and macroinvertebrates. No significant correlation was found between macroinvertebrates and sum of absolute values of RWLF, while WLD showed significant influence on some biotic parameters. In spring, WLD did not cause significant effect to macroinvertebrates (P > 0.05). In summer, however, the influence was significant, especially in the area of the downstream (XX01 - XX02) of the Xiangxi Bay (P < 0.05). The middle reach of the bay (XX05), located in the conjunction area between Xiangxi Bay and a secondary tributary of the TGR, was also affected significantly (P < 0.05). The relative abundance of Tubificidae declined with the increase of the WLF, while abundance of Chironomidae increased. The time lags of the influence to macroinvertebrates were about 15 days. This analysis indicated that WLF in the mainstream of the reservoir mainly influences the downstream of the tributary bay, and also affects the conjunction area of the secondary tributary. Chironomidae are more tolerant than Tubificidae in water-body with dramatic disturbance, therefore can be considered as the indicator of the effect of summer WLF on macroinvertebrates.     

Cross‐sectional epidemiological study on the lead burden of children and workers in Greece

Exposure of the general population to lead in the environment is mainly caused by motor traffic exhaust and by industrial pollution. The aim of the study in Greece was to assess lead exposure in children living in point source impacted areas (Lavrion and Aspropyrgos‐Eleusis) using the biological monitoring parameter “blood lead concentration”;.

In addition, workers of a lead smelter, a battery plant and an oil refinery were investigated in these areas at the same time.

Five hundred and thirty‐four children and 105 workers took part in this investigation.

The highest blood lead levels (mean: 24.16 μg/100ml; range: 10.40–60.49 μg/100 ml) were found in children living in a 500m‐area around the lead smelter at Lavrion. Blood lead decreases corresponded to the increasing distance from the emitter. Nevertheless the values of children living in a 1500 m distance to the smelter are significantly higher than those of children living next to other kinds of industrial lead sources.

The mean values of the children living in the two industrial towns were manifold higher than those of the control group.

The blood lead levels of the investigated workers did not exceed the German BAT‐value (Biologischer Arbeitsstoff‐Toleranzwert) of 70 μg/100ml.     

Sorption‐desorption kinetics of some organochlorine insecticides in silt‐water suspensions

Kinetic (batch) sorption and desorption experiments for some organochlorine insecticides in silt‐water suspensions are described. The effect of possible experimental artifacts on the results is examined. The influence of the silt/water ratio on the linear sorption coefficient and on the “nonextractable”; solute fraction is determined. The sorption process is described in terms of some kinetic models.     

Aqueous high‐temperature chemistry of arsenic‐containing compounds in water at 300°C

Arsenic compounds, and especially organo‐arsenic derivatives, are highly toxic and many have been manufactured as chemical warfare agents. This study was designed to provide background information relevant to the potential application of aquathermolysis techniques for the detoxification of such potent military warfare agents. Six arsenic‐containing compounds with structural features which mimic known agents were studied in neutral superheated water: 4‐aminophenylarsine oxide, 4‐arsanilic acid, 4‐nitrophenylarsonic acid, 5, 10‐dihydro‐10‐ethylphenarsazine, tetraphenylarsonium chloride hydrate, and (3‐cyanopropyl)dimethyl(2‐phenethyl)arsonium bromide. Most of these compounds were moderately susceptible to hydrolysis for 1h at 300°C. o‐ and p‐Aminosubsituted arsenic compounds were more reactive than compounds with an electron‐withdrawing group substituent. Aromatic C—As bonds were more resistant to cleavage than aliphatic C—As bonds.     

Rose Bengal‐sensitized photooxygenation of chlorohydroxyaromatic contaminants in water: A kinetic study

A kinetic study of the RB‐sensitized photooxygenation of a series of chlorohydroxyaromatic (ClArOH) water contaminants (phenolic and dihydroxybenzene derivatives) has been carried out. In addition, an exhaustive study on the possible interactions of RB electronically excited triplet and singlet states with ClArOH was also developed. The determination of relative rates of oxygen uptake upon sensitized irradiation, employing auxiliar selective quenchers of oxygen active species, indicate the contribution of both singlet molecular oxygen (ca. 71%) and Superoxide ion (ca. 26%) as the reactive pathways for ClArOH degradation. The substitution by chlorine atoms in position meta greatly decrease the photooxygenation rate of the phenolic derivatives. For the dihydroxybenzene series, increase in nuclear chlorination parallels a decrease in the photodegradation rate.

Outdoors sensitized solar irradiation experiments on different ClArOH mixtures leads to measurable levels of oxygen after a few minutes exposure. From the environmental point of view, and ruling out the possibility of direct‐irradiation photoreactions, sensitized photooxygenation appears as an alternative pathway for ClArOH degradation, in competence with other naturally‐occurring photoprocesses involving reactive transient species.     

Long‐term desorption kinetics of Cu2+from biosorbent in water and seawater

A long‐term study of the desorption kinetics of Cu²⁺from biosorbent materials in water and seawater environments was carried out. The biosorbents were un‐treated and pre‐treated biomass of marine alga Durvillaea potatorum.The pre‐treatment of the biomass was carried out with calcium chloride (CaCl₂) solution followed by thermal treatment. The biosorbents were loaded with Cu²⁺in batch adsorption experiments and the desorption kinetics were measured in water and seawater in static batch desorption experiments for a period over 10 months. The physical and structure characteristics of the biosorbents were also examined under a microscope. The un‐treated biosorbent structure completely broke down in 2 and 1 months in water and seawater environments, respectively. The pre‐treatment procedure applied improved the biosorbent stability and its long term desorption rate was extremely low.     

Photochemistry of halogenated benzene derivatives. part xii.∗ effects of sodium nitrite on the environmental phototransformation of bromoxynil (3,5‐dibromo‐4‐hydroxybenzonitrile) herbicide in water: The photoincorporation of nitrite ions into bromoxynil

Photoreactions of the herbicide bromoxynil (3,5‐dibromo‐4‐hydroxybenzonitrile) (1) were extensively studied in water containing various concentrations of sodium nitrite with radiation of wavelengths around 313 nm. In the absence of NaNO₂, the quantum yields for the photodecomposition of the herbicide I amounted to 0.054±0.005, while such data was in the range of 0.047 ±0.005 to 0.023 ±0.003 in the presence of 0.5 to 25.0 × 10^‐3 m of the inorganic salt. These quantum yield data for the phototransformation of 1 without and with the presence of sodium nitrite followed the Stern‐Volmer equation. The rates of the photolytic destruction of bromoxynil (1) in water were slower in the presence than in the absence of NaNO₂. For example, the irradiation of the 7.8 x 10^‐6M aqueous solution of 1 in the presence of 10 mM sodium nitrite gave rise to the production of three main photoproducts, viz., 3‐bromo‐4‐hydroxy‐5‐nitrobenzonitrile (2), 4‐hydroxy‐3‐nitrobenzonitrile (3), and an “unidentified photoproduct”; 4. In the case of this photoreaction of compound 1, the percentages of maximum concentration of the photoproducts 2, 3, and 4 were achieved after 14, 44.5, and 60‐min photolyses of 1, respectively; the starting material 1 completely disappeared after 60‐min photolysis. The photoproducts 2 and 3 were identified through the interpretation of the GC‐MS data. Both thhe mass and FT‐IR spectra of the product 4 indicated the possible presence of a COOH group in 4.     

17α-Ethinylestradiol in Lakes of Hanoi and its effect on seed germination

Abstract

The lakes of Hanoi are important water resources for urban agriculture. The concentrations of 17α-ethinylestradiol in the water of three major lakes were found to range from 0.1 to 9.1?ng/L, peaking during the rainy season. Effects at levels from 1?ng/L to 1?µg/L on the germination of mung bean (Vigna radiata) and bok choy (Brassica rapa) were studied. Soaking the seeds in solutions containing 17α-ethinylestradiol at 10?ng/L and higher increased the germination rate of mung bean but not of bok choy. For the latter, irrigation after sowing with solutions containing 17α-ethinylestradiol at 10?ng/L and higher accelerated germination.

Abbreviations: MNRE: Ministry of Natural Resources and Environment; PE₆₀: Population equivalent; USGS: U.S. Geological Survey; SPE: Solid phase extraction; EDTA: Disodium ethylenediaminetetraacetate; HPLC: High performance liquid chromatography; ELISA: Enzyme-linked immunosorbent assay; DOM: Dissolved organic matter; EEQ: Estradiol equivalent     

Effects of the Ellagic acid on the N‐Acetyltransferase activity and Acetylation of 2‐aminofluorene in the rat

The effects of the ellagic acid on the in vitro and in vivo acetylation of 2‐aminofluorene were investigated in male Sprague‐Dawley rats. For in vitro examination, cytosols with or without ellagic acid co‐treatment showed different percentage of 2‐aminofluorene acetylation. For in vivo examination, pre‐treatment of male rats with ellagic acid (10 mg/kg) 24h prior to the administration of 2‐aminofluorene (50 mg/kg) resulted in a 26% and 29%, respectively, decrease in the urinary and fecal recovery of N‐acetyl‐2‐aminofluorene, and a 37% decrease in the metabolic clearance of 2‐aminofluorene to N‐acetyl‐2‐aminofluorene. This is the first demonstration that ellagic acid decrease the N‐acetylation of carcinogens in vitro and in vivo.     

Determination of pentachlorophenol in human urine using solid phase extraction and GC‐MS analysis with stable isotope dilution

A method for the determination of pentachlorophenol (PCP) in human urine was developed. Urine samples were fortified with ¹³C₆‐IabeIed PCP and hydrolyzed with sulfuric acid prior to extraction. The urine samples were then passed through preconditioned solid phase extraction cartridges containing octadecylsilane adsorbent. The PCP was subsequently eluted from the cartridge with ethyl acetate and converted to pentachloroanisole prior to GC‐MS analysis. GC‐MS quantitation was performed using the technique of stable isotope dilution. Percent recoveries averaging 100, 97, and 111% were obtained for replicate urine samples fortified with approximately 2, 20, and 200 ng/mL of PCP, respectively. The method detection limit was estimated to be 0.2 ng/mL.     

Transport of butyltins at the water‐air interface and the adsorptive behavior of tributyltin in the surface microlayer

The transfer dynamics and enrichment phenomena of monobutyltin chloride(MBT), dibutyltin chloride(DBT) and tributyltin chloride(TBT) at the water‐surface microlayer (SM) interface were studied. The transport processes of the three compounds at the interface are very fast in the estuarine environment. The mass transfer coefficients are 1.54 m/h for MBT, 2.16 m/h for DBT, 1.56 m/h for TBT. The effect of various factors, including pH, salinity, suspended particulate and temperature, on the adsorptive behavior of TBT in the water's surface microlayer was also studied.     

Effect of Florasulam on soil residues and enzyme activity of wheat in drylands北大核心CSCD

Florasulam is a three azole and pyrimidine sulfonamide herbicide, mainly used for weeds prevention and control in winter wheat fields. The main purpose of this experiment was to study the effects of different doses of Florasulam on soil residues and on the enzymatic activity of wheat cultivated in drylands, and to provide the theoretical basis for a scientific use of florasulam. Five doses (0, 15, 30, 45, and 60 mL/667 m2) of Florasulam were applied in order to detect differences in soil residue content and enzymatic activities. Soil residues and enzymatic activities (catalase, phosphatase, urease, dehydrogenase) were measured and analyzed after the 5 different doses of Florasulam were processed. The residual amount of Florasulam in the soils decreased gradually with the growth phase of wheat, and was lower than that of 0.01 mg/kg. The residual amount of Florasulam in different soil layers gradually decreased with the increase of soil thickness. The enzymatic activity of soils treated with Florasulam was basically T3 > T2 > T1 > CK > T4, where T3 was the highest, whereas T4 could inhibit the enzymatic activity. Under these experimental conditions, in order to decrease soil pollution and lower Florasulam residues, it is recommended to apply Florasulam at a concentration range of 30 to 45 mL/667 m2 © 2018 Science Press. All rights reserved.     

Photodegradation of pesticides .1. Photolysis rates and half‐life of acylanilides and their major metabolites in water

The photolysis in water solution of three fungicides (Metalaxyl, Benalaxyl, and Furalaxyl) was studied under artificial light. At λ = 254 Benalaxyl and Furalaxyl underwent fast degradation with rearrangement reactions less complex than those of Metalaxyl. Under A = 254–290 the photolysis was very fast and Benalaxyl and Furalaxyl show a common behaviour. This was found to be a kinetic consecutive process leading, at first, to N‐2,6‐xylyl‐D,L‐alaninate (II), which was degraded to 2,6‐dimethylaniline (IV). This amine gives unknown products. Metalaxyl underwent a parallel/consecutive photodegradtion to give (II) and N‐(methoxyacetyl)‐2,6‐dimethylaniline (VI). While (II) was easily converted to (IV) as earlier, (VI) was more stable to photolysis. Under λ > 290 all the fungicides shown very slow degradation with pseudo first order rate constants. The photoproducts were degraded faster than the parent compounds by factors from 13 to 1800. The presence of photosensitizer in water (humic acids or acetone) resulted in total decomposition of fungicides and of their photoproducts.     

Improvement of sampling and analytical methods for polychlorinated dibenzo‐p‐dioxins and dibenzofurans in environmental samples and its quantitative evaluation

Sampling of PCDDs/Fs in flue gas from a MSW incinerator was conducted using a modified apparatus of the 5 train method, which has been widely used for the sampling of PCDDs/Fs emission. In the atmosphere a high volume air sampler with special packings was used. Collection efficiencies of PCDDs/Fs were more than 98% for both samplers, using ¹³C₁₂—PCDD reference standard isomers. It was suggested that these sampling methods were adaptable for the measurements of PCDDs/Fs at sources and in the environment. To validate the applicability of existing methodologies on the PCDD/F determination, interlaboratory comparisons were undertaken. From high resolution GC/MS analysis, 2,3,7,8‐TCDD concentrations in reference ash samples were 0.052±0.013 ng/g as comparable results between the laboratories. In addition, the daily intakes of PCDDs/Fs for exposed persons in the MSW incineration facilities in Japan were estimated ranging of 0.053 to 0.28 pg/kg/day by the international toxic equivalent calculations.