Cellular metabolism of arsenic studied in mammalian cellsin vitro

The cytotoxicity of trivalent and pentavalent inorganic arsenic was studied in cultured mouse fibroblasts. Concentrations of As(III) in the M range and approximately 10-fold higher concentrations of As(V) led to a reduction of cellular proliferation and viability with a concomitant increase of LDH release and stimulation of lactate production. Cells pretreated with a low As(III) concentration were less sensitive to toxic doses of As(III) or As(V).Uptake of As(III) by the cells was greater than that of As(V). Both forms of inorganic arsenic were converted intracellularly to monomethylarsonic (MMA) and dimethylarsinic (DMA) acids, which were subsequently released into the culture medium. In As-pretreated cells, which proved more resistant to As toxicity, biotransformation of inorganic to MMA and DMA was increased.     

Investigation of acetaminophen adsorption with a biosorbent as a purification method of aqueous solution

ABSTRACT

Pharmaceutical compounds are considered emerging environmental pollutants that have a potential harmful impact on environment and human health. In this study, the spiky green horse-chestnut shell was used for the biosorption and removal of acetaminophen from aqueous solution. It was analysed how the parameters, like contact time, pH, mass of biosorbent and temperature, influence the effectiveness of acetaminophen removal from aqueous solutions. The equilibrium was quickly achieved after 10?min (～60%). The amount of acetaminophen adsorption slightly increased with the increase of the mass of biosorbent, and for example for an aqueous solution containing 10?mg/L of acetaminophen adsorption was increased from 62% to 81%. The promising results obtained at pH ranged between 2 and 9, which shows that the adsorption of acetaminophen did not depend on the pH and it may be a consequence of the predominant microporous sorbent and its surface charge. The result is better correlated to a pseudo-second-order kinetic model of type 2 (r ²?=?0.9992) than pseudo-first-order. A sorption mechanism of acetaminophen on biosorbent was also proposed. The sorption of acetaminophen over biosorbent is mainly preceded by hydrophilic interactions between hydroxyl and carbonyl groups in pharmaceutical molecules and hydroxyl and carboxyl groups on the surface of biosorbent.     

The influence of seawater temperature on zooid size and growth rate in Pentapora fascialis (Bryozoa: Cheilostomata)

Zooid size variation and growth banding in the bryozoan Pentapora fascialis, collected from the South of Great Britain to the South of Italy, were investigated in order to test their relationship with the variation of seawater temperature. Zooid length appeared to be more sensitive than zooid area and width to temperature variation. The longest zooids were budded in localities that typically experience low seasonal variation in temperature (3.2–7.5°C) and low mean annual temperature (about 11°C). Zooid length demonstrated the strongest relationship with the range of seasonal variation in temperature rather than the mean annual temperature. Growth bands produced during colder months were less high than those produced during warmer months. Measurements of these alternating bands were used to calculate growth rate of the laminae, ranging from 20.7 at Plymouth to 29.3 mm year⁻¹ at Tino Island. Significant differences in zooid length were found between the two bands, with longer zooids within the band developed in colder months and shorter zooids in bands produced in the warmer period. We conclude that zooid size can be used as an environmental proxy of the seasonal temperature regimes experienced by the species.     

Decrease of Pb bioavailability in solis by addition of phosphate ions

Bioavailability of Pb in contaminated soils can be highly decreased by conversion of labile Pb species into pyromorphite Pb₅(PO₄)₃Cl, induced by amendment with a phosphate source. However, PO₄ ³⁻ can be specifically adsorbed on goethite α-Fe(OH)₃ present in soils. We demonstrate that despite the stability of phosphate ions adsorbed on goethite surface, the reaction between goethite-adsorbed phosphates and aqueous lead in the presence of Cl⁻ results in crystallization of pyromorphite. Two morphological forms of pyromorphite formed on goethite were observed: 1) incrustations, indicating direct reaction of Pb and Cl ions with PO₄ ³⁻ adsorbed on goethite surface, and 2) aggregates of pyromorphite crystals indicating that the reaction with PO₄ ³⁻ ions took place in the volume of the solution. This suggests that precipitation of pyromorphite is faster than desorption of phosphates and that aqueous Pb may serve as a sink for phosphate ions by shifting the equilibrium and inducing PO₄ ³⁻ desorption.     

塔基图穆保护区——库克群岛的社区所属生态旅游明星

塔基图穆保护区 1996年创建于库克群岛的拉罗汤加岛 , 其目标是为了当前和未来生产者的利 益而对生物多样性实施保护 . 只有当地人民对其土地和资源拥有所有权 . 生态旅游将成为该 保护区的主要经济活动 . 在土地所有者同意和支持下 , 一个有指导的 " 大自然漫步 " 已经组 织起来 .     

Pilot study of sources of lead exposure in Moscow,Russia

This preliminary investigation of sources of lead exposure in Moscow, Russia, by Russian and US collaborators measured lead in paint, interior dust, and drinking water in seven day-care centres, and in petrol, soil and canned food. Some paint samples exceeded US regulatory standards for lead in paint on surfaces (0.5%). Dust lead loadings were < 1.7 g cm^–2 and below the guidance levels of the US EPA. Drinking water lead concentrations were at or below the US drinking water standard of 15 g L^–1. Lead concentrations in petrol from Moscow vehicles and petrol stations were consistent with a regulation banning the sale of leaded petrol within the Moscow City limits. Except for baby food, lead levels were higher in the Russian canned foods (range 6 to 1240 g kg^–1, dry weight) compared to corresponding US canned foods, with ratios of Russian to US levels of up to 120:1 for evaporated milk. Lead concentrations in soil generally ranged from 500 to 2000 g g^–1, levels that would trigger hazard reduction measures according to US EPA guidance. These findings, together with the use of lead in petrol outside Moscow, indicate multiple sources of lead exposure in Russia. Priorities for future research are discussed including the establishment of interlaboratory quality control programmes.     

In situ biodegradation determined by carbon isotope fractionation of aromatic hydrocarbons in an anaerobic landfill leachate plume (Vejen,Denmark)

Concentrations and isotopic compositions (13C/12C) of aromatic hydrocarbons were determined in eight samples obtained from the strongly anoxic part of the leachate plume downgradient from the Vejen Landfill (Denmark), where methanogenic, sulfate-reducing and iron-reducing conditions were observed. Despite the heterogeneous distribution of the compounds in the plume, the isotope fractionation proved that ethylbenzene and m/p-xylene were subject to significant biodegradation within the strongly anoxic plume. The isotope fractionation factors (alphaC) for the degradation of the m/p-xylene (1.0015) and ethylbenzene (1.0021) obtained from the field observations were similar to factors previously determined for the anaerobic degradation of toluene and o-xylene in laboratory experiments, and suggest that in situ biodegradation is one major process controlling the fate of these contaminants in this aquifer. The isotope fractionation determined for 1,2,4-trimethylbenzene and 2-ethyltoluene suggested in situ biodegradation; however, the isotopic composition did not correlate well with the respective concentration as expressed by the Rayleigh equation. Some other compounds (1,2,3-trimethylbenzene, o-xylene, naphthalene and fenchone) did not show significant enrichments in delta13C values along the flow path. The compound concentrations were too low for accurate isotope analyses of benzene, toluene, 1- and 2-methylnaphthalene, while interferences in the chromatography made it impossible to evaluate the isotopic composition for 4-ethyltoluene, 1,3,5-trimethylbenzene and camphor.In addition to demonstrating the potential of assessing isotopic fractionation as a means for documenting the in situ biodegradation of complex mixtures of aromatic hydrocarbons in leachate plumes, this study also illustrates the difficulties for data interpretation in complex plumes and high analytical uncertainties for isotope analysis of organic compounds in low concentration ranges.     

Hydrogen peroxide photolysis, fenton reagent and photo-fenton for the degradation of nitrophenols: a comparative study

The kinetics of the degradation of seven nitrophenols (2-nitrophenol, 4-nitrophenol, 2,5-dinitrophenol, 2,6-dinitrophenol, 2,4-dinitrophenol, 2-methyl-4,6-dinitrophenol, 4-methyl-2,6-dinitrophenol) with the Fenton reagent, photo-Fenton, and hydrogen peroxide photolysis was investigated. The efficiency and operating costs for the studied treatments were evaluated and compared. The Fenton reagent was found to be the most efficient and the cheapest way for the nitrophenols (NPs) degradation. The formation of nitrate as a result of mineralisation of organically bounded nitrogen was observed during the treatment of NPs with studied treatment processes. The degrees of organically bounded nitrogen conversion to nitrate after 90% degradation of NPs with the Fenton, photo-Fenton and hydrogen peroxide photolysis were 51-67%, 85-90%, and 50-60%, respectively. According to Daphnia magna acute toxicity test, the Fenton treatment led to complete detoxification of NPs.     

Photocatalytic degradation of volatile organic compounds at the gas-solid interface of a TiO2 photocatalyst

In the present work, photocatalytic degradation of volatile organic compounds including gas-phase trichloroethylene (TCE), acetone, methanol and toluene over illuminated TiO2 was closely examined in a batch photoreactor as a function of water vapor, molecular oxygen and reaction temperature. Water vapor enhanced the photocatalytic degradation rate of toluene, but was inhibitive for acetone, and, there was an optimum water vapor concentration in the TCE and methanol removal. In a nitrogen atmosphere, it showed lower photocatalytic degradation rate than in air and pure oxygen. Thus, it could be concluded that oxygen is an essential component in photocatalytic reactions by trapping photogenerated electrons on the semiconductor surface and by decreasing the recombination of electrons and holes. As for the influence of reaction temperature, it was found that photocatalytic degradation was more effective at a moderate temperature than at an elevated temperature for each compound.     

Remediation of arsenic-contaminated soils and washing effluents

Laboratory experiments were conducted to determine the distribution of various arsenic species in tailings and soils. Other specific goal of the tests were to evaluate the extraction efficiency of arsenic using alkaline or acid washing, to determine optimum operational parameters of alkaline washing, and to evaluate the arsenic precipitation of washing effluents by pH adjustment or ferric chloride addition. Alkaline washing using sodium hydroxide was found to be favorable in removing arsenic from tailings or soils having a higher portion of arsenic in the operationally defined crystalline mineral fraction of crystalline oxide and amorphous aluminosilicates. This is due to the ligand displacement reaction of hydroxyl ions with arsenic species and high pH conditions that can prevent readsorption of arsenic because predominant negatively charged crystalline oxides do not attract the negatively charged oxyanions. For tailings, sodium hydroxide had 10-20 times higher extraction efficiencies than hydrochloric- or citric acid. The optimum concentration of sodium hydroxide for soil washing was determined to be 200 mM for all samples, while the optimum ratios were 10:1 and 5:1 for tailings and field/river sedimentary soils, respectively. The washing effluent of river soil was effectively treated by adjusting pH to 5-6 with hydrochloric acid, resulting in arsenic concentrations of <50 microgl(-1). In the case of field soil effluent, an addition of ferric chloride with a minimum mass ratio of 11 (Fe/As) was needed to reduce the arsenic below 50 microgl(-1).