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581.
Phenylated arsenic compounds occur as highly toxic contaminants in former military areas where they were formed as degradation products of chemical warfare agents. Some phenylarsenic compounds such as roxarsone and aminophenylarsonic acids were applied as food additive and veterinary drugs in stock-breeding and therefore pose an environmental risk in agricultural used sites. Very few data exist in the literature concerning uptake and effects of phenylarsenic compounds in plants growing on contaminated soils. In this study, the accumulation, extractability, and metabolization of five different phenylarsenic compounds, phenylarsonic acid, p- and o-aminophenylarsonic acid, phenylarsine oxide, and 3-nitro-4-hydroxyphenylarsonic acid called roxarsone, by the terrestrial plant Tropaeolum majus were investigated. Ion chromatography coupled to inductively coupled plasma mass spectrometry was used to differentiate these arsenic compounds, and inductively coupled plasma atomic emission spectroscopy was used for total arsenic quantification. All compounds considered were taken up by the roots and transferred to stalks, leaves, and flowers. The strongest accumulation was observed for unsubstituted phenylarsonic acid followed by its trivalent analogue phenylarsine oxide that was mostly oxidized in soil whereas the amino- or nitro- and hydroxy-substituted phenylarsonic acids were accumulated to a smaller degree.The highest extraction yield of 90% for ground leaf material was achieved by 0.1 M phosphate buffer, pH 7.7, in a two-step extraction with a total extraction time of 24 h. The extraction of higher amounts of arsenic (50–70% of total arsenic present in leaves depending on arsenic species application) from non-ground intact leaves with deionized water in comparison with the buffer (20–40% of total arsenic) is ascribed to osmotic effects. The arsenic species analysis revealed a cleavage of the amino groups from the phenyl ring for plants treated with aminophenylarsonic acids. A further important metabolic effect consisted in the production of inorganic arsenate and arsenite from the phenylated arsonic acid groups. 相似文献
582.
Bulk deposition of polycyclic aromatic hydrocarbons (PAHs) in an industrial site of Turkey 总被引:1,自引:0,他引:1
Ambient air and deposition samples were collected in the period of July 2004-May 2005 in an industrial district of Bursa, Turkey and analyzed for polycyclic aromatic hydrocarbon (PAH) compounds. The overall average of fourteen bulk deposition fluxes for PAHs was 3300+/-5100 ng m(-2) d(-1). PAH depositions showed a seasonal variation and they were higher in winter months. This was probably due to increases in residential heating activities and decreases in atmospheric mixing layer levels. Ambient air samples, measured with a high volume air sampler, were collected from the same site. The average total concentration including gas and particulate phase was about 300+/-420 ng m(-3) and it was in the range of previously reported values. Some of the ambient air and bulk deposition samples were collected simultaneously in dry periods. Both concurrently measured values were used to calculate the dry deposition velocities whose overall average value was 0.45+/-0.35 cm s(-1). 相似文献
583.
The study aimed to explore if changes in crown defoliation and stem growth of Scots pines (Pinus sylvestris L.) could be related to changes in ambient ozone (O3) concentration in central Europe. To meet this objective the study was performed in 3 Lithuanian national parks, close to the ICP integrated monitoring stations from which data on meteorology and pollution were provided. Contribution of peak O3 concentrations to the integrated impact of acidifying compounds and meteorological parameters on pine stem growth was found to be more significant than its contribution to the integrated impact of acidifying compounds and meteorological parameters on pine defoliation. Findings of the study provide statistical evidence that peak concentrations of ambient O3 can have a negative impact on pine tree crown defoliation and stem growth reduction under field conditions in central and northeastern Europe where the AOT40 values for forests are commonly below their phytotoxic levels. 相似文献
584.
585.
Determination of phenolic and steroid endocrine disrupting compounds in environmental matrices 总被引:4,自引:1,他引:3
Arditsoglou A Voutsa D 《Environmental science and pollution research international》2008,15(3):228-236
BACKGROUND, AIM AND SCOPE: Many pollutants have received significant attention due to their potential estrogenic effect and are classified as endocrine disrupting compounds (EDCs). EDCs comprise many classes of organic compounds. The development or optimization of analytical protocols for the simultaneous determination of EDCs in environmental samples is an analytical challenge because these compounds exhibit different physicochemical characteristics, they occur in the aquatic environment in relatively low concentrations and, furthermore, environmental samples are considered as complex matrices. The aim of this study is the development of analytical methods for the simultaneous determination of phenolic and steroid EDCs in aqueous and solid samples. The target compounds are 4-nonylphenol, 4-octylphenol, their ethoxylate oligomers (mono- and di-ethoxylates of nonylphenol and octylphenol), bisphenol A, the estrogens (estriol, estrone, 17beta-estradiol, 17alpha-estradiol) and the synthetic steroids (mestranol and 17alpha-ethynylestradiol). MATERIALS AND METHODS: Solid phase extraction employing Oasis HLB cartridges and different elution solvents was used for the recovery studies of the target compounds from various types of water samples (ultrapure water, artificial seawater, river water and seawater). Ultrasonic assisted extraction was applied for the recovery of the target EDCs from the solid samples. The recoveries were assessed using various solvents for the extraction and the elution of EDCs from different SPE cartridges used for clean up. Gas chromatography-mass spectrometry after derivatization with N,O-bis(trimethylsilyl)-trifluoroacetamide was employed for the determination of these compounds. RESULTS AND DISCUSSION: The recovery rates of three elution solvents (methanol, acetone and ethylacetate) for the extraction of target EDCs from artificial seawater were assessed after preconcentration on SPE cartridges. Acetone showed better recoveries and was further tested for its extraction efficiency in different water types (river water, seawater). Ultrasonic assisted extraction was used for the recovery of target EDCs from solid matrices. Acetone, methanol, mixture of acetone-methanol (1:1) and ethylacetate were used as extraction solvents. Ethylacetate and the mixture of acetone-methanol (1:1) exhibited better extraction efficiencies. An additional clean up step was necessary for sediment samples. Different SPE cartridges were employed for clean up of the extracts (Oasis HLB, C18, Florisil, silica, combination of silica and alumina). Florisil cartridges were finally used. The proposed methods were further validated on the determination of target EDCs in field collected samples (river water, seawater, wastewater, total suspended solids and sediments) from the major area of Thessaloniki, Greece. CONCLUSIONS: Efficient and accurate integrated methods for the simultaneous determination of alkylphenols (nonylphenol, octylphenol), their ethoxylate oligomers (mono- and di-ethoxylate of nonylphenol and octylphenol), bisphenol A and steroids (estriol, estrone, 17beta-estradiol, 17alpha-estradiol, mestranol and 17alpha-ethynylestradiol) in aqueous and solid samples were developed. The proposed methods were applied for the determination of the target compounds in representative environmental samples in the area of Thessaloniki, Northern Greece. RECOMMENDATIONS AND PERSPECTIVES: This study confirms the occurrence of selected EDCs in inland and marine waters in the area of Thessaloniki, Northern Greece. Since there is no previous data on the occurrence of the target EDCs in the major area, an extended survey is in progress to evaluate the occurrence and fate of these compounds. 相似文献
586.
对流层臭氧(O3)主要由氮氧化物(NOx)和挥发性有机物(VOCs)经过一系列光化学反应生成,反应过程呈现复杂的非线性关系.为深入了解O3的光化学特征及生成机制,利用2018年夏季大气O3与VOCs的观测数据,结合大气零维框架模拟模型F0AM-MCM,研究O3超标日和非O3超标日的O3光化学特征之间的差异性.观测结果表明,O3超标日期间φ(O3)和φ(TVOCs)的平均值分别为47.8×10-9和49.0×10-9,为非O3超标日期间O3(26×10-9)和TVOCs(30×10-9)体积分数的1.8倍和1.6倍.使用F0AM模型,借助EKMA曲线和RIR分析等识别O3敏感性,发现南京市O3超标日和非O3超标日O3的形成均主要受VOCs和NOx的协同控制.F0AM-MCM模拟结果表明,在O3超标日,·OH和HO2的日平均混合比分别是非O3超标日的1.3倍和1.8倍,表明O3超标日期间具有更强的大气氧化能力,且·OH和HO2的形成和损失速率也有明显的增加,表明自由基循环的增强.此外,O3超标日的O3生成速率明显高于非O3超标日,从而导致了O3超标日的O3净生成速率明显高于非O3超标日.以上发现提高了对南京夏季O3超标日大气O3光化学特征的认识. 相似文献
587.
The possibility of finding new medicines from natural sources is one of the more commonly cited reasons for preserving biodiversity,
and employing indigenous knowledge of traditional healing remedies greatly increases the likelihood of discovering these hidden
medicinal compounds. The main difficulties in using natural products as a source for pharmaceutical lead compounds involve
separating the plethora of compounds from the original extract, as well as the gamble of time and money invested in an activity
that may not yield a novel compound. However, while these difficulties exist, the potential of natural products still far
outweighs the limitations of the simple structures and known modes of action of synthetic lead compounds. As such, the production
of novel medicines, particularly for cancer and human immunodeficiency virus (HIV) treatments as well as the inhibition of
antibiotic-resistant bacteria, now requires the utilization of natural products. This paper provides a review of the current
methods used in elucidating pharmaceutical lead compounds from natural sources, focusing on plant samples in particular. 相似文献
588.
589.
挥发性有机物的控制技术及其发展 总被引:6,自引:0,他引:6
介绍了挥发性有机物的来源、危害、排放标准及常见控制技术,同时对处理技术的新发展进行了总结和展望。 相似文献
590.