黄土丘陵沟壑区生态风险时空动态及其风险分区—以陕西省米脂县为例

目前,黄土丘陵沟壑区等生态脆弱区生态风险评估已成为地理学与生态学应对生态系统管理的研究热点之一。以黄土丘陵沟壑区米脂县为研究区,构建“风险概率—敏感性—损失度”（PSI）的三维评价框架,并以子流域为评价单元进行数据整合,分析了米脂县2009-2015年准则层与综合生态风险的时空分异及其重心转移,并基于风险主导因子给出米脂县风险防范分区及降险对策。结果如下：（1）2009-2015年风险概率分别为49.93%、52.92%,有上升趋势;生境敏感性分别为0.61、0.60,下降了1.6%,生境质量趋好;损失度分别为0.42、0.46,损失度增加。（2）生态风险呈现中间高南北低的空间分布;研究期间生态风险值分别为0.14、0.15,风险有所升高;风险重心向西南转移跃入银州川道且风险演化主体方向为西北—东南走向。（3）风险预警区、生态恢复区、预警恢复兼顾区、自然调控区面积占比分别为7.53%、6.57%、23.86%、62.04%。基于风险主导因子的风险防范分区可有效进行风险消解,促进区域生境的可持续。     

Importance of nutrient availability for soluble microbial products formation during a famine period of activated sludge: Evidence from multiple analyses

Much remains unknown about compositional variations in soluble microbial products (SMP) with the shift of the substrate condition from a feast to a famine phase in biological treatment systems. This study demonstrated that the formation of SMP could be suppressed by up to 75% during the famine phase with the addition of essential nutrients. In contrast, presence of electron acceptor did not play any significant role during the stress condition, showing the similar amounts of SMP (r?=?0.98, p?<?0.05) formation between the bioreactors supplied with air and N₂. The SMP formed in the famine phase was more bio-refractory in the famine versus the feast phase with a linear correlation shown between the production and their aromatic structures in the composition (R²?>?0.95). The fluorescence excitation–emission matrix coupled with parallel factor analysis (EEM-PARAFAC) revealed the presence of four different fluorescent components, including two protein-like (C1 and C4), fulvic-like (C2), and humic-like (C3) components, in the SMP and bEPS formed at different conditions. Both C1 and C4 showed increasing trends (R²?>?0.95) with the length of starvation in the bioreactors without essential nutrients. Nutrient availability was found to be a key factor to quench the production of large-sized biopolymers. This study provides a wealth of information on operation conditions of activated sludge treatment systems to minimize large sized SMP molecules (particularly proteins), which typically exert many environmental concerns to effluent organic matter quality.     

Simultaneous quantification of fifty-one odor-causing compounds in drinking water using gas chromatography-triple quadrupole tandem mass spectrometry

A wide range of compounds with various structural features can cause taste and odor(TO)problems in drinking water. It would be desirable to determine all of these compounds using a simple analytical method. In this paper, a sensitive method combining liquid–liquid extraction(LLE) with gas chromatography-triple quadrupole tandem mass spectrometry(GC–MS/MS)was established to simultaneously analyze 51 odor-causing compounds in drinking water,including organic sulfides, aldehydes, benzenes, phenols, ethers, esters, ketones, nitrogenous heterocyclic compounds, 2-methylisoborneol and geosmin. Three deuterated analogs of target analytes, dimethyl disulfide-d6, benzaldehyde-d6 and o-cresol-3,4,5,6-d4,were used to correct the variations in recovery, and five isotope-labeled internal standards(4-chlorotoluene-d4, 1, 4-dichlorobenzene-d4, naphthalene-d8, acenaphthene-d10, phenanthrene-d10 respectively) were used prior to analysis to correct the variations arising from instrument fluctuations and injection errors. The calibration curves of the target compounds showed good linearity(R2 0.99, level = 7),and method detection limits(MDLs) below 1/10 of the odor threshold concentrations were achieved for most of the odorants(0.10–20.55 ng/L). The average recoveries of most of the analytes in tap water samples were between 70% and 120%, and the method was reproducible(RSD 20%, n = 7). Additionally, concentrations of odor-causing compounds in water samples collected from three drinking water treatment plants(DWTPs) were analyzed by this method.According to the results, dimethyl trisulfide, dimethyl disulfide and indole were considered to be the key odorants responsible for the swampy/septic odor. 2-Methylisoborneol and geosmin were detected as the main odor-causing compounds for musty/earthy odor in DWTP B.     

One-step synthesis of Cu(II) metal–organic gel as recyclable material for rapid, efficient and size selective cationic dyes adsorption

Efficient removal of non-biodegradable and hazardous dyes from wastewater remains a hot research topic. Herein, a rationally designed a Cu(Ⅱ)-based metal–organic gel(Cu-MOG) with a nanoporous 3 D network structure prepared via a simple one-step mixing method was successfully employed for the removal of cationic dyes. The Cu-MOG exhibited high efficiency, with an adsorption capacity of up to 650.32 mg/g, and rapid adsorption efficiency, with the ability to adsorb 80% of Neutral Red within 1 min. The high adsorption efficiency was attributed to its large specific surface area, which enabled it to massively bind cationic dyes through electrostatic interaction, and a nanoporous structure that promoted intra-pore diffusion. Remarkably, the Cu-MOG displayed size-selective adsorption, based on adsorption studies concerning dyes of different sizes as calculated by density functional theory. Additionally, the adsorption performance of the Cu-MOG still maintained removal efficiency of 100% after three regeneration cycles. These results suggested that the Cu-MOG could be expected to be a promising and competitive candidate to conveniently process wastewater.     

淮河上游全新世黄土-土壤剖面重金属元素分布与环境变化

在野外考察研究的基础上利用X-射线荧光光谱仪测定了河南禹州全新世YPC黄土-土壤剖面Zn、Cu、Co、Ni、Nb、Pb、V、Cr、Mn、Ti重金属元素的含量及其变化,研究表明在黄土堆积期,重金属元素的含量都很低,变化幅度也很小,可作为衡量古土壤层成壤改造的背景值.在全新世古土壤和现代表土中这些元素含量却大大增加,说明在温暖湿润的时期,成壤改造使易溶易迁移元素的淋失导致重金属元素的相对富集.而Pb含量从8cm深度处向上急剧增加,增幅达60%,这是大气污染物沉降积累的客观记录.     

矿渣与工业废渣改良黄土的性能与机理研究进展

黄土在世界上分布面积较广,在我国也有约60×104 km2的分布,具有湿陷性是其区别于其它区域性土的最显著特点,并由此引发造成各种地质灾害和工程问题.采用石灰、水泥或高分子材料等对其进行改性以达到消除湿陷性或提高黄土强度的目的,是岩土工程领域的重要课题.选用矿渣和工业废渣作为改性参料,用以研究改性黄土的力学特性变化和改...     

我国不同矿物气溶胶源区物质的物理化学特征

在我国不同的矿物气溶胶源区进行采样分析的结果表明,源区气溶胶物质的物理化学特性相差很大.黄土的颗粒最细,91%的黄土颗粒可以形成矿物气溶胶进行长距离输送;沙土较粗,只有15%的沙尘颗粒可以形成矿物气溶胶;2个煤灰样品的粒径差异较大,抚顺煤灰中＜74μm的颗粒高达39%,而呼和浩特煤灰只有7%.不同粒径颗粒的化学分析结果表明,微量元素在细颗粒上有较高的富集.黄土与沙漠土壤的细颗粒的化学性质十分相似,同煤灰的化学性质完全不同,其常量元素与A1的比值(E/Al)十分接近,而且与深海沉积物粘土中的比值(E/A1)     

添加不同化合态结合的铜离子对其在黄土中吸持及形态的影响

分别以CuSO4和Cu(NO3)2为吸持质，研究了添加不同化合态结合的铜离子在黄土中的等温吸持及形态分布规律。结果表明：黄土吸持铜离子以碳酸盐结合态为主。当铜离子初始浓度较低时，添加不同化合态结合的铜离子对其在黄土中的吸持及碳酸盐结合态没有明显影响；当铜离子初始浓度超过一定值时，添加不同化合态结合的铜离子对其在黄土中的吸持及碳酸盐结合态的影响随铜离子初始浓度的增加而明显增大。添加不同化合态结合的铜离子，其持有量和碳酸盐结合态含量均随土壤浓度的增大而减小。当铜离子初始浓度较低时，添加不同化合态结合的铜离子对其在黄土中的吸持量及碳酸盐结合态含量随土壤浓度的变化影响不大；当铜离子初始浓度超过一定值时，相同初始浓度条件下CuSO4较Cu(NO3)2会造成更大幅度的变化。     

表面活性剂对可离子化有机化合物在黄土中吸附行为的影响

研究了2，4-二氯苯酚、2，4-二硝基苯酚和苯甲酸三种可离子化有机化合物在天然黄土和阳离子表面活性剂改性黄土中的吸附行为。讨论了DH值、离子强度和二价重金属阳离子对可离子化有机化合物在改性黄土中吸附的影响。提出了可离子化有机化合物在改性黄土中的吸附模型，吸附等温曲线可分解为两条分别代表离子和非离子形态的等温吸附曲线；其吸附行为可用双模式吸附理论来解释。在2，4-二硝基苯酚共存时，苯甲酸在改性黄土中的吸附量减小，证明竞争吸附的存在。     

兰格缪尔等温式的适用性分析——以黄土吸持铜离子为例

在不同土壤浓度条件下进行了黄土对铜离子的等温吸持实验（包括吸附与沉淀）。利用兰格缪尔（Langmuir）等温式对实验结果进行拟合时发现：黄土对铜离子的吸持结果在形式上仍可用传统的Langmuir等温式来描述，但式中的相关参数已经不再具有原来的物理意义。本文分析了Langmuir等温式在黄土对铜离子吸持时的适用性，指出其参数变化与铜离子的吸附关系不大，而与沉淀密切相关。