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621.
Silvia Maggioni Patrick Balaguer Claudia Chiozzotto Emilio Benfenati 《Environmental science and pollution research international》2013,20(3):1649-1660
We investigated contamination by endocrine-disrupting chemicals in drinking water from 35 major Italian cities and five popular Italian brands of bottled mineral water. The quality of Italian drinking water was assessed by combing chemical analysis with bioassay to quantify specific estrogenic contaminants and to characterize the actual biological effect of the mixture of chemicals present in drinking water including the contribution of not targeted compounds. The selected contaminants were natural and synthetic steroid estrogens, alkylphenols and bisphenol A, linuron, triazine herbicides, and their metabolites. A specific analytical method was developed based on solid phase extraction of 1 L of water and concentration to 100 μL for quantification by electrospray ionization liquid chromatography tandem mass spectrometry, achieving quantification limits of 0.05–0.36 ng/L for herbicides and 0.64–7.70 ng/L for steroids and phenols. No steroid estrogens were detected in any of the samples, while bisphenol A and nonylphenols were detected in the ranges of 0.82–102.00 and 10.30–84.00 ng/L respectively. Herbicides and their degradation products, when present, were found from slightly above the quantification limits up to 49.91 ng/L, mainly from cities in northern Italy. Chemical analyses were complemented by the performance of a bioassay for the determination of the estrogenic activity in the extracts based on the transactivation of estrogen receptor α-transfected reporter HeLa-ERE-Luciferase-Neomycin cell line. Activity was generally low with maximum estrogenicity of 13.6 pg/L estradiol equivalents. 相似文献
622.
Elena Marañón Leonor Castrillón Juan José Fernández Yolanda Fernández Ana Isabel Peláez Jesús Sánchez 《Journal of the Air & Waste Management Association (1995)》2013,63(2):137-143
Abstract Different autonomous communities located in northern Spain have large populations of dairy cattle. In the case of Asturias, the greatest concentration of dairy farms is found in the areas near the coast, where the elimination of cattle manure by means of its use as a fertilizer may lead to environmental problems. The aim of the present research work was to study the anaerobic treatment of the liquid fraction of cattle manure at mesophilic temperature using an upflow anaerobic sludge blanket (UASB) reactor combined with a settler after a pasteurization process at 70 °C for 2 hr. The manure used in this study came from two different farms, with 40 and 200 cows, respectively. The manure from the smaller farm was pretreated in the laboratory by filtration through a 1-mm mesh, and the manure from the other farm was pretreated on the farm by filtration through a separator screw press (0.5-mm mesh). The pasteurization process removed the pathogenic microorganisms lacking spores, such as Enterococcus, Yersinia, Pseudomonas, and coliforms, but bacterial spores are only reduced by this treatment, not removed. The combination of a UASB reactor and a settler proved to be effective for the treatment of cattle manure. In spite of the variation in the organic loading rate and total solids in the influent during the experiment, the chemical oxygen demand (COD) of the effluent from the settler remained relatively constant, obtaining reductions in the COD of ~85%. 相似文献
623.
UV/TiO(2) photocatalysis of phenylmercury salts in aqueous solutions has been performed starting from both acetate (C(6)H(5)HgCH(3)CO(2), PMA) and chloride (C(6)H(5)HgCl, PMC) salts, in the presence or the absence of oxygen at acidic pH. Removal of Hg(II) in solution took place with the simultaneous deposit of dark or pale gray solids on the photocatalyst, identified as metallic Hg (when starting from PMA) or mixtures of Hg(0) and Hg(2)Cl(2) (when starting from PMC). Partial mineralization of the organic part of both compounds has also been achieved. Hg(II) removal and mineralization were enhanced in the absence of oxygen. PMA photocatalysis followed a saturation kinetics, going from first order at low concentration to zero order at higher concentrations (>0.5mM). For PMA, reaction was faster at high pH (11) with formation of mixtures of Hg and HgO. Phenol was detected as a product of the reaction in both cases, PMA and PMC, and no formation of dangerous methyl- or ethylmercury species was observed in the first case. A mechanism for the photocatalytic reaction has been proposed. The fact that calomel was found as a deposit when starting from PMC under nitrogen suggests that the mechanism of Hg(II) transformation proceeds through successive one-electron transfer reactions passing by mercurous forms. 相似文献
624.
Solanum nigrum grown in contaminated soil: effect of arbuscular mycorrhizal fungi on zinc accumulation and histolocalisation 总被引:1,自引:0,他引:1
Marques AP Oliveira RS Samardjieva KA Pissarra J Rangel AO Castro PM 《Environmental pollution (Barking, Essex : 1987)》2007,145(3):691-699
Zn tissue accumulation in Solanum nigrum grown in a non-contaminated and a naturally contaminated Zn matrix and the effect of inoculation with different arbuscular mycorrhizal fungi (AMF) on metal uptake were assessed. S. nigrum grown in the contaminated soil always presented higher Zn accumulation in the tissues, accumulating up to 1622 mg Zn kg(-1). The presence of both Glomus claroideum and Glomus intraradices enhanced the uptake and accumulation of Zn by S. nigrum (up to 83 and 49% higher Zn accumulation, respectively). The main deposits of the metal were found in the intercellular spaces and in the cell walls of the root tissues, as revealed by autometallography, with the inoculation with different AMF species causing no differences in the location of Zn accumulation. These findings indicate that S. nigrum inoculated with selected heavy metal tolerant AMF presents extracting and accumulating capacities, constituting a potentially suitable remediation method for Zn polluted soils. 相似文献
625.
Boulaid M Aguilera A Busonera V Camacho F Monterreal AV Valverde A 《Journal of environmental science and health. Part. B》2007,42(7):809-815
An analytical method, using supercritical fluid extraction (SFE), was assessed for residue analysis of the insecticides fipronil, acrinathrin and pyridaben and the fungicide kresoxim-methyl in melons. Extraction conditions were optimized on glass beads, as inert material, evaluating different pressures, temperatures, and CO(2) volumes. Also, the extractability of pesticides from hydromatrix and anhydrous magnesium sulfate was evaluated. Both adsorbents were evaluated for the preparation of SFE-spiked melon samples. Extractions of fortified samples were done using 20 mL of CO(2), 300 atm, and 50 degrees C. Different extraction conditions, including the addition of water and methanol as a static modifier, were used to assess the extractability of these pesticides, and the addition of methanol was demonstrated to improve the extraction of all the studied pesticides. 相似文献
626.
Seixas TG Kehrig Hdo A Costa M Fillmann G Di Beneditto AP Secchi ER Souza CM Malm O Moreira I 《Environmental pollution (Barking, Essex : 1987)》2008,154(1):98-106
Selenium and total and organic mercury were determined in the liver and kidney of franciscana dolphin (Pontoporia blainvillei) incidentally caught in fishing nets along two Brazilian coastal areas (southeast and south). Regional differences in the concentrations of these contaminants were observed in P. blainvillei. Liver showed the highest organic and total mercury. In general, samples of individuals collected at the southern of Brazil had the highest concentrations of selenium and total and organic mercury. No significant gender differences were observed. Growth stage influenced the accumulation of these contaminants in both organs, and hepatic concentrations increased with the body length, according to the sampling area. Molar mercury and selenium concentrations in liver were significantly correlated, with a Se:Hg ratio close to 4. The among-site differences we found may be related to differences in preferred prey, bioavailability in the marine environment, environmental conditions, or these individuals may belong to distinct populations. 相似文献
627.
Díaz-de-Mera Y Aranda A Bravo I Rodríguez D Rodríguez A Moreno E 《Environmental science and pollution research international》2008,15(7):584-591
Background, aim, and scope The adverse environmental impacts of chlorinated hydrocarbons on the Earth’s ozone layer have focused attention on the effort
to replace these compounds by nonchlorinated substitutes with environmental acceptability. Hydrofluoroethers (HFEs) and fluorinated
alcohols are currently being introduced in many applications for this purpose. Nevertheless, the presence of a great number
of C–F bonds drives to atmospheric long-lived compounds with infrared absorption features. Thus, it is necessary to improve
our knowledge about lifetimes and global warming potentials (GWP) for these compounds in order to get a complete evaluation
of their environmental impact. Tropospheric degradation is expected to be initiated mainly by OH reactions in the gas phase.
Nevertheless, Cl atoms reaction may also be important since rate constants are generally larger than those of OH. In the present
work, we report the results obtained in the study of the reactions of Cl radicals with HFE-7000 (CF3CF2CF2OCH3) (1) and its isomer CF3CF2CF2CH2OH (2).
Materials and methods Kinetic rate coefficients with Cl atoms have been measured using the discharge flow tube–mass spectrometric technique at 1 Torr
of total pressure. The reactions of these chlorofluorocarbons (CFCs) substitutes have been studied under pseudo-first-order
kinetic conditions in excess of the fluorinated compounds over Cl atoms. The temperature ranges were 266–333 and 298–353 K
for reactions of HFE-7000 and CF3CF2CF2CH2OH, respectively.
Results The measured room temperature rate constants were k(Cl+CF3CF2CF2OCH3) = (1.24 ± 0.28) × 10−13 cm3 molecule−1 s−1and k(Cl+CF3CF2CF2CH2OH) = (8.35 ± 1.63) × 10−13 cm3 molecule−1 s−1 (errors are 2σ + 10% to cover systematic errors). The Arrhenius expression for reaction 1 was k
1(266–333 K) = (6.1 ± 3.8) × 10−13exp[−(445 ± 186)/T] cm3 molecule−1 s−1 and k
2(298–353 K) = (1.9 ± 0.7) × 10−12exp[−(244 ± 125)/T] cm3 molecule−1 s−1 (errors are 2σ). The reactions are reported to proceed through the abstraction of an H atom to form HCl and the corresponding halo-alkyl
radical. At 298 K and 1 Torr, yields on HCl of 0.95 ± 0.38 and 0.97 ± 0.16 (errors are 2σ) were obtained for CF3CF2CF2OCH3 and CF3CF2CF2CH2OH, respectively.
Discussion The obtained kinetic rate constants are related to the previous data in the literature, showing a good agreement taking into
account the error limits. Comparing the obtained results at room temperature, k
1 and k
2, HFE-7000 is significantly less reactive than its isomer C3F7CH2OH. A similar behavior has been reported for the reactions of other fluorinated alcohols and their isomeric fluorinated ethers
with Cl atoms. Literature data, together with the results reported in this work, show that, for both fluorinated ethers and
alcohols, the kinetic rate constant may be considered as not dependent on the number of –CF2– in the perfluorinated chain. This result may be useful since it is possible to obtain the required physicochemical properties
for a given application by changing the number of –CF2– without changes in the atmospheric reactivity. Furthermore, lifetimes estimations for these CFCs substitutes are calculated
and discussed. The average estimated Cl lifetimes are 256 and 38 years for HFE-7000 and C3H7CH2OH, respectively.
Conclusions The studied CFCs’ substitutes are relatively short-lived and OH reaction constitutes their main reactive sink. The average
contribution of Cl reactions to global lifetime is about 2% in both cases. Nevertheless, under local conditions as in the
marine boundary layer, τ
Cl values as low as 2.5 and 0.4 years for HFE-7000 and C3H7CH2OH, respectively, are expected, showing that the contribution of Cl to the atmospheric degradation of these CFCs substitutes
under such conditions may constitute a relevant sink. In the case of CF3CF2CF2OCH3, significant activation energy has been measured, thus the use of kinetic rate coefficient only at room temperature would
result in underestimations of lifetimes and GWPs.
Recommendations and perspectives The results obtained in this work may be helpful within the database used in the modeling studies of coastal areas. The knowledge
of the atmospheric behavior and the structure–reactivity relationship discussed in this work may also contribute to the development
of new environmentally acceptable chemicals. New volatile materials susceptible of emission to the troposphere should be subject
to the study of their reactions with OH and Cl in the range of temperature of the troposphere. The knowledge of the temperature
dependence of the kinetic rate constants, as it is now reported for the case of reactions 1 and 2, will allow more accurate
lifetimes and related magnitudes like GWPs. Nevertheless, a better knowledge of the vertical Cl tropospheric distribution
is still required. 相似文献
628.
Kelly L. Zellars Pamela L. Perrewé Ana M. Rossi Bennett J. Tepper Gerald R. Ferris 《组织行为杂志》2008,29(5):549-571
The present study examined whether employees high in negative affectivity (NA) are destined to experience strain at a higher level than those low in NA. We used data collected from 230 employees to investigate the moderating effects of political skill, as a form of interpersonal control, on the relationship between NA and physiological strain. As hypothesized, NA was positively related to physiological strain (i.e., facial muscle tension as measured by electromyography (EMG)), and political skill buffered this effect such that the relationship was weaker among employees who were higher in political skill. Tests of mediated moderation further suggested the means by which political skill moderates the NA/strain relationship; specifically, the results were consistent with the idea that perceived control and, in turn, job‐related efficacy explain the moderating effect of political skill. Strengths and limitations of the study, practical implications, and directions for future research are discussed. Copyright © 2007 John Wiley & Sons, Ltd. 相似文献
629.
Parente TE De-Oliveira AC Paumgartten FJ 《Environmental pollution (Barking, Essex : 1987)》2008,152(1):233-238
The induction of cytochrome P4501A-mediated activity (e.g. ethoxyresorufin-O-deethylation, EROD) has been used as a biomarker for monitoring fish exposure to AhR-receptor ligands such as polycyclic aromatic hydrocarbons (PAH), polychlorinated biphenyls (PCB) and polychlorinated dibenzo-dioxins/furans (PCDD/Fs). In this study we found that hepatic EROD is induced in fish ("Nile tilapia", Oreochromis niloticus and "acará", Geophagus brasiliensis) from the Guandu River (7-17-fold) and Jacarepaguá Lake (7-fold), Rio de Janeiro, Brazil. Since both cichlid fish are consumed by the local population and the Guandu River is the main source of the drinking water supply for the greater Rio de Janeiro metropolitan area, pollution by cytochrome P4501A-inducing chemicals is a cause for concern and should be further investigated in sediments, water and biota. We additionally showed that EROD activity in the fish liver post-mitochondrial supernatant-simpler, cheaper and less time consuming to prepare than the microsomal fraction-is sufficiently sensitive for monitoring purposes. 相似文献
630.
Gómez MJ Malato O Ferrer I Agüera A Fernández-Alba AR 《Journal of environmental monitoring : JEM》2007,9(7):718-729
The present work provides a multi-residue analytical method for determining a selection of 20 pharmaceuticals from diverse therapeutical classes in hospital effluent wastewater. The method is based on the simultaneous extraction of the target compounds by solid phase extraction (SPE), followed by liquid chromatography-time-of-flight-mass spectrometry (LC-TOF-MS) analysis. Using TOF-MS, accurate mass measurements within 2 ppm error were obtained for most of the pharmaceuticals studied. Empirical formula information can be obtained by this method, allowing the unequivocal identification of the target compounds in the samples. Validation studies showed that LC-TOF-MS analysis is a valuable new tool for identification and quantification of pharmaceuticals in wastewater. Recoveries, using Oasis HLB cartridges at pH 7, were higher than 75% for all pharmaceuticals, except for ranitidine, 4-methylaminoantipyrine (4-MAA), cefotaxime and omeprazole, which needed specific pH conditions for their extraction. Linearity of response over two orders of magnitude was demonstrated (r > 0.99). Matrix effects resulting in suppression of the response were observed. For most of the compounds ion suppression was less than 39%, except for metronidazole, carbamazepine 10,11-epoxide, naproxen and erythromycin, where the signal suppression was 42%, 59%, 46% and 95%, respectively. A simple and effective approach to minimize or avoid matrix interferences was the 1 : 4 dilution of the SPE extracts. Method detection limits (MDLs) and quantification limits (MQLs) ranged between 4-115 ng l(-1) and 14-384 ng l(-1), respectively. The precision of the method, calculated as relative standard deviation (RSD), ranged from 1.1-19.8% and 1.7-21.7% for intra- and inter-day, respectively. The developed analytical method was applied to the analysis of hospital effluent wastewater during a survey study. 18 of the 20 pharmaceuticals studied were detected at concentration levels of microg l(-1), reaching in some cases concentrations over 100 microg l(-1), and in the case of the analgesic and antipyretic dipyrone metabolite, higher than 1000 microg l(-1). 相似文献