Altitudinal Distribution of Meltwater and Its Effects on Glacio‐Hydrology in Glacierized Catchments,Central Asia

In glacierized catchments, elevation is correlated with meltwater through its association with temperature, precipitation, and glacier hypsometry. The revelation of the altitudinal distribution of meltwater, unattended and not fully understood in previous work, might provide a better understanding of climate change impacts on glacio‐hydrology. Here, critical zone approach was defined and applied in 12 glacierized catchments of the Tien Shan–Pamir–Karakorum Mountains, Central Asia using manually calibrated glacier‐enhanced Soil and Water Assessment Tool model over 1966–2005. The critical zone, a sequence of elevation bands with above‐average snow and glacier melt, contributes maximum meltwater to total runoff. The critical zone shared 37%–95% (average = 80%) of meltwater contributions to total runoff, although its size was only 13%–30% of the total elevational relief. The critical zone controlled 76% and 82% variability in relative changes of glacier area and total runoff at the catchment scale, respectively. The increase in temperature was identified as the dominant driver for variations in total runoff in all catchments except Vakhsh and Yurungkash, where precipitation change remained dominant. Overall, glacier hypsometry limited the first‐order control of meltwater distributions on glacio‐hydrology. It is concluded that critical zone approach can interpret the proxy role of elevation to affect water availability under climate and glacier area change in glacierized catchments.     

Spectroscopic study of the degradation of antibiotics and the generation of representative EfOM oxidation products in ozonated wastewater

This study examined effects of ozonation on thirteen fluoroquinolone, macrolide and lincosamide antibiotics present in municipal wastewater. Transformations of effluent organic matter (EfOM) caused by ozonation were characterized using absorbance/fluorescence spectroscopy and high performance size exclusion chromatography (HPSEC). Concentrations of aldehydes and carboxylic acids generated via the oxidation of EfOM were also determined. The absorbance and fluorescence of ozonated wastewater decreased with increasing ozone dose or treatment time. HPSEC data showed that these phenomena corresponded to the oxidation of all EfOM fractions, with some preference towards the degradation of the EfOM molecules with high apparent molecular weight. The removal of antibiotics and production of aldehydes and carboxylic acids were strongly correlated with the changes in both EfOM absorbance and fluorescence. Applications of a model describing the concurrent degradation of trace level contaminants and relative changes of EfOM emission allowed achieving a good fitting between the experimental and modeled ΔC/C₀ vs. ΔA/A₀ and ΔC/C₀ vs. ΔF/F₀ data.     

Assessment of aquatic experimental versus predicted and extrapolated chronic toxicity data of four structural analogues

The present study was developed to assess the chronic toxicity predictions and extrapolations for a set of chlorinated anilines (aniline (AN), 4-chloroaniline (CA), 3,5-dichloroaniline (DCA) and 2,3,4-trichloroaniline (TCA)). Daphnia magna 21 d chronic experimental data was compared to the chronic toxicity predictions made by the US EPA ECOSAR QSAR tools and to acute-to-chronic extrapolations. Additionally, Species Sensitivity Distributions (SSDs) were constructed to assess the chronic toxicity variability among different species and to investigate the acute versus chronic toxicity in a multi-species context.Since chlorinated anilines are structural analogues with a designated polar narcotic mode of action, similar toxicity responses were assumed. However, rather large interchemical and interspecies differences in toxicity were observed. Compared to the other three test compounds, TCA exposure had a significantly larger impact on growth and reproduction of D. magna. Furthermore, this study illustrated that QSARs or a fixed ACR are not able to account for these interchemical and interspecies differences. Consequently, ECOSAR was found to be inadequate to predict the chronic toxicity of the anilines and the use of a fixed ACR (of 10) led to under of certain species. The experimental ACRs determined in D. magna were substantially different among the four aromatic amines (ACR of 32 for AN, 16.9 for CA, 5.7 for DCA and 60.8 for TCA). Furthermore, the SSDs illustrated that Danio rerio was rather insensitive to AN in comparison to another fish species, Phimphales promelas. It was therefore suggested that available toxicity data should be used in an integrative multi-species way, rather than using individual-based toxicity extrapolations. In this way, a relevant overview of the differences in species sensitivity is given, which in turn can serve as the basis for acute to chronic extrapolations.     

Removal potential of anti-estrogenic activity in secondary effluents by coagulation

Anti-estrogenic activity in wastewater is gaining increased attention because of its endocrine-disrupting function. In this study, the level and removal efficiency by coagulation of anti-estrogenic activity in secondary effluents of domestic wastewater treatment plants were studied. Anti-estrogenic activity was detected in secondary effluent samples at a tamoxifen (TAM) equivalent concentration level of 0.38–0.94 mg-TAM L⁻¹. Dissolved organic matters (DOM) with the molecular weight (MW) less than 3000 Da in hydrophobic acids (HOA) and hydrophobic neutrals (HON) fractions of the secondary effluent were the key fractions related to anti-estrogenic activity. Coagulation with FeCl₃ and polyaluminium chloride (PAC) can remove the anti-estrogenic activity of the secondary effluents, but the removal efficiency was limited. The removal efficiency using FeCl₃ coagulant was higher than that induced by PAC. Dissolved organic carbon was continuously removed with increased coagulant dose (0–120 mg L⁻¹ FeCl₃ or 0–60 mg L⁻¹ PAC). However, the removal of anti-estrogenic activity was not enhanced further when the coagulant concentration was beyond a critical value (30 mg L⁻¹ FeCl₃ or 10 mg L⁻¹ PAC). The highest removal of anti-estrogenic activity was about 36% by FeCl₃ and 20% by PAC. Size exclusion chromatography results indicated difficulty in removing DOM with MW less than 3000 Da in the secondary effluent during coagulation even at a high coagulant concentration, which led to low removal efficiency of anti-estrogenic activity.     

西安城北地区秋季PM_(2.5)中的矿尘颗粒污染特征

采用单颗粒气溶胶飞行时间质谱仪(Single Particle Aerosol Mass Spectrometer,SPAMS)对西安市大气矿尘颗粒物进行连续12 d在线分析,共采集到107 425个同时含有正负质谱信息的矿尘颗粒,矿尘颗粒物占PM_(2.5)样本数的8.44%。结果表明,矿尘颗粒物的正离子碎片成分以Na~+、K~+、Al~+、Ca~+、CaO~+、Fe~+为主,同时还含有Pb~+等,负离子碎片成分以NO~-_2和NO~-_3为主,另外还含有HSO~-_4、SiO~-_3、HSiO~-_3、H(NO_3)~-_2等。在西安市大气细颗粒物中,矿尘颗粒物中贡献较大的几类(如含钙、含铁、铁氧颗粒物等)大多是老化的成分。将观测阶段采集到的矿尘颗粒纳入本地污染源谱进行来源分析,其主要来源为扬尘源、工业源、燃煤源和汽车尾气源等。     

2008年北京市PM_(10)的粒度分布分形维数变化特征

2007年11月-2008年10月间在北京市市中心和西北城区采集了不同季节的PM10样品,并借助扫描电子显微镜和图像分析软件对其进行粒度分布分形维数分析。结果表明,颗粒物中细颗粒物越多,粒度越细,则颗粒物粒度分布分形维数值越大。2008年西北城区的PM10的粒径分布分形维数较大,市中心的较小。市中心的粒度分布分形维数在1.95～2.59之间,各个季节的分形维数呈现冬季春季夏季秋季,西北城区的粒度分布分形维数在2.58～2.72,各个季节的分形维数呈现秋季夏季冬季春季,说明在市中区冬季PM10粒度较细,而在西北城区秋季的颗粒物偏细。与2005年同季相比,2008年的总体颗粒物和烟尘集合体的粒径分布分形维数较大,矿物颗粒的粒度分布分形维数较小,并且总分布的季节变化一致。2008奥运期间的PM10粒度分布分形维数在2.28～3.39之间变化,标志着颗粒物总体变细的趋势。     

泥石流研究中的粒度分析方法及其应用

粒度分析是泥石流研究的一个重要手段,是它的基础实验之一。本文介绍了在泥石流研究中一些较常用的及有应用前景的粒度分析方法,它们包括:频率累积曲线、直方图、概率累积曲线、粒度参数统计、粒度参数散点图等;对粒度分析在泥石流的分类、物理参数的计算、水力学条件的分析等方面的作用也做了一些初步的探讨。     

Distribution of Platinum group elements in road dust in Beijing metropolitan area, China

Dust samples collected from the Beijing metropolitan area (China) were evaluated to determine the distribution and the concentration of platinum group elements (PGEs). The dust particles that were smaller than 100 mesh size fraction (150 μm) were analyzed after aqua regia digestion. Concentrations[RL2] of Pt, Rh, and Pd were found to be between 3.96 and 356.3 ng/g, 2.76 and 97.11 ng/g, and 0.1 and 124.9 ng/g, respectively, in the urban areas of Beijing, whereas for the background samples collected from the suburbs of Beijing, the concentration of Pt, Pd, and Rh were very low and ranged from 0.1 to 0.9 ng/g, 0.5 to 1.4 ng/g, and 0.8 to 2.2 ng/g, respectively. The[RL3] distributions of PGEs in road dust were an accurate reflection of the levels of pollution and were found to match with the local traffic conditions. A strong positive correlation was established among all the elements found in road dust. This suggests that emissions of abraded fragments from vehicle exhausts may be the source of the high concentration of Pt, Rh, and Pd in road dust along the main roads of Beijing.