北京大气PM2.5中微量元素的浓度变化特征与来源

为了解北京大气细粒子中微量元素的污染水平和来源,在车公庄和清华园进行了连续1年、每周1次的PM_2.5采样和全样品分析.微量元素浓度的周变化大,尤以冬季为甚,相邻2周最大相差达1.6倍;但除冬季的平均浓度较高之外,其季节变化并不显著.微量元素的富集因子在春季最低,反映了频繁发生的沙尘天气的影响.Se、Br和Pb的浓度比来自于北京A层土壤中的含量要高出约1000～8000倍,表明它们主要来自于人为污染.其中Se的富集度最高,反映了北京细粒子来自于燃煤污染的特征.Pb的年均浓度(0.31μg·m^-3)虽然未超过WHO的年均标准,但与洛杉矶和布里斯班相比处于较高的水平;与Br、Se的比较分析表明,燃煤可能是Pb除机动车排放之外的另一个重要来源.     

Quantification of pesticide residues on plastic mulching films in typical farmlands of the North China

• Pesticide residuals on mulching film of Shandong, Tianjin and Hebei. • Detected 29 pesticides in soil and 30 in mulching film. • Pesticides on plastic films: 86.4‒22213.2 ng/g and in soil: 9.3‒535.3 ng/g. • Pesticides on plastic films 20 times higher than in soil. Plastic debris as new pollutants attracts much attention in the recent years. The plastic mulching films is one of the most important plastic debirs source in the environment. The aim of this work was to investigate the current status of pesticide residues on the plastic mulching films. Based on the QuEChERS method, multi-residue methods for detection of pesticide residues with gas chromatography tandem mass spectrum (GC-MS) and high performance liquid chromatography tandem mass spectrum (HPLC-MS) were developed for the analysis of the pesticides residues in plastic film and soil samples from Tianjin, Hebei and Shandong. The total concentrations of pesticide residues were in the range of 86.4‒22213.2 ng/g in plastic film debris, which was about 20 times higher than that in soil (9.3‒535.3 ng/g). Residual level of pesticides varied greatly in different samples. The historical usage and recent application of pesticides were the main sources for pesticide residues on plastic films and soil. In short, plastic mulching films could act as a sink for pesticides in farmland and the ubiquitous pesticide residues on plastic films should draw more attention.     

溴氰菊酯对大鼠肝微粒体酶的影响

本实验研究了溴氰菊酯对雄性大鼠肝微粒体苯胺羟化酶活力和细胞色素P-450含量的影响。结果发现溴氰菊酯在动物体内能降低苯胺羟化酶活力(23.80％)和细胞色素P-450含量(21.18％)。该效应与微粒体脂质过氧化反应无关,亦与肝细胞破坏或内质网膜通透性的改变无关。溴氰菊酯本身对肝微粒体酶并不呈现抑制作用,当用肝微粒体酶诱导剂苯巴比妥诱导肝微粒体酶后,溴氰菊酯降低微粒体酶活性的效应消失。这表明溴氰菊酯降低肝微粒体酶的作用可能与其干扰肝微粒体酶蛋白的合成有关。     

Cu、Zn、Cd、Hg对青海弧菌(Q67菌株)联合毒性作用的研究

采用等毒性混合法（equitoxicmixture）探讨了Cu、Zn、Cd、Hg对青海弧菌（Q67菌珠）的联合毒性作用。当两种金属作用时,Zn和Cd为拮抗作用,Cu和Zn为加和作用,Cu和Cd、Cu和Hg、Zn和Hg、Cd和Hg均为协同作用。而当3种或4种金属同时作用时,联合毒性作用均趋向于加和作用,其机理还有待于进一步研究。     

物种敏感度分布的非参数核密度估计模型

针对目前物种敏感度分布参数方法建模所存在的缺点,首次提出基于非参数核密度估计方法的物种敏感度分布模型,并提出相应的最优窗宽和检验方法。选用无机汞作为案例研究对象,利用非参数核密度估计方法和3种传统参数模型分别推导了保护我国水生生物的无机汞的急性水质基准值。结果表明,非参数核密度估计方法在推导无机汞水质基准中的稳健性和精确度都大大优于传统参数模型,能够更好地构建物种敏感度分布曲线。该方法的提出丰富了水质基准的理论方法学,为更好地保护水生生物提供了有力的支撑。     

二噁英类化合物的毒性作用机制及其生物检测方法

二噁英类化合物具有高毒性,来源多样且分布广泛,是持久性有机物的典型代表,二噁英类污染物及其对健康的危害已引起了公众的普遍关注。一些二噁英类同系物具有代谢稳定性,其毒性效应主要是通过芳香烃受体介导,而越来越多的研究表明二噁英类毒性作用机制的复杂性。在此背景下,综述了近些年在二噁英类毒性作用机制及其代谢途径的新认识,评价比较了主要二噁英类高通量生物检测方法,以期为该类污染物的环境污染物筛查和风险评估提供参考。     

高碑店湖表层水中雌激素的分布及其光降解影响因素

雌激素等内分泌干扰物在水体中普遍存在,其在再生水中的存在以及在水体中的迁移转化会产生潜在的健康和生态风险。光降解是水体中雌激素消除的主要途径之一,水体中共存的无机离子及有机质等对雌激素的光解存在不同的影响。对高碑店湖再生水体中雌激素的污染状况进行了调查,结果显示表层水中天然雌激素雌酮(E1)和人工合成雌激素17α-乙炔基雌二醇(EE2)的浓度最高。在模拟太阳光照射条件下对E1在水溶液中的降解规律及影响因素进行了研究,发现在模拟1 SUN的光密度条件下,15 min时E1降解率可达85%(C0=5μg·L-1),而氨氮对E1的光降解存在一定的抑制作用,并且抑制作用随着氨氮的升高而变大。与纯水系统相比,高碑店湖表层水基质中E1的光降解速率较低,说明整体上氨氮、HCO-3、浊度等因素对E1光降解产生的抑制作用占主导。对雌酮及其降解产物进行了红外光谱分析,结果显示1 720 cm-1对应的C=O键特征峰在光照时间为0、10和20 min样品中的强度逐渐减弱,而2 854 cm-1和2 925 cm-1对应的脂肪碳的C-H键特征峰先增强后减弱,可能是因为E1结构中的C-C=O发生了反应生成了C=C-OH,而随着反应的继续,C=C也被进一步氧化,但降解产物的结构需要进一步研究推断。随着E1的光降解,E1水溶液的内分泌干扰活性逐渐下降,氨氮虽然对E1的光降解有一定的抑制作用,但随着降解反应的进行E1水溶液的内分泌干扰活性依然呈下降趋势。     

Abatement of sulfide generation in sewage by glutaraldehyde supplementation and the impact on the activated sludge accordingly

Hydrogen sulfide emission in sewer systems is associated with toxicity, corrosion, odour nuisance and high costs treatment. In this study, a novel method to inhibit sulfide generation from sewage by means of glutaraldehyde supplementation has been suggested and evaluated under anaerobic conditions. Different concentrations of glutaraldehyde at 10, 15, 20, 30 and 40 mg·L^-1 have been investigated. Besides, the possible impacts of glutaraldehyde supplementation on an activated sludge system and an appraisal of the economic aspects are presented as well. As observed from the experimental results, a dosage of 20 mg·L^-1 glutaraldehyde resulted in a significant decrease of the sulfide production by 70%–80% in the simulated sewage. Moreover, the impacts of additional glutaraldehyde at 20 mg·L^-1 on activated sludge, in terms of chemical oxygen demand removal and oxygen uptake rates, were negligible. From an economical point of view, the cost of the commercial glutaraldehyde products required in the operation, which was calculated on the basis of activated sulfide removal avoidance, was around €3.7–4.6 S·kg^-1. Therefore it is suggested that glutaraldehyde supplementation is a feasible technique to abate the sulfide problems in sewer systems. Yet further research is required to elucidate the optimum “booster” dosage and the dosing frequency in situ accordingly.     

Review on the study of mercury/silver ions-pyrimidine base pairs in DNA duplexes and their application in detection technology北大核心CSCD

Nucleic acids and their analogues are getting more and more attention. Metal-mediated base pairs as a kind of simple and functionalized nucleic acids in special positions have widened the scope of application of functional nucleic acids and their analogues. In this type of base pairs, the representative is the interaction between metal ions and pyrimidine bases, especially the research on thymine-Hg2+-thymine (T-Hg2+-T) and cytosine-Ag+-cytosine (C-Ag+-C) base pairs. This review summarizes the structure and mechanism of metal-mediate pyrimidine base pairs as well as the application in the biochemical analysis. It explores the mode and ratio of coordination between metal ions and base pairs, the effects on the stability of DNA helical structure, the related crystal structure and the three-dimensional configuration information in the DNA helix. The analytical application mainly includes various probes of metal ions, small molecules, protein and the detection of single nucleotide polymorphism. Among them the most widely used metal ions detection, and its combination with spectrum technology, visualization and amplification technology greatly promoted the rapid development of sensitive detection technology. In further studies, it is necessary to reveal the mechanism of interaction between T-Hg2+-T and C-Ag+-C, and more attention should be paid to combining of T-Hg2+-T and C-Ag+-C base pairs with other new technologies. The scope of practical application should also be further extended.     

TiO_2/PTh/Fe_3O_4催化剂制备及光催化与磁回收性能

以聚噻吩磁性微珠PTh/Fe3O4(PF)为载体,采用低温水热法(170℃,pH=7±0.2)在其表面负载TiO2,制备了壳/壳/核结构的磁载光催化剂TiO2/PTh/Fe3O4(TPTF)。用透射电子显微镜(TEM)、X射线衍射仪(XRD)、傅里叶红外分光光度计(FT-IR)、振动样品磁强计(VSM)对催化剂的形貌、物相组成、表面性质、磁学性质进行了表征。以苯酚为模拟污染物,评价其光催化活性;通过自制的磁回收装置,考察其磁回收特性。结果表明,TiO2晶粒大小在4~6 nm之间,具有混晶结构(锐钛矿型占93.6%,金红石型占6.4%);当nTiO2∶n噻吩单体∶nFe3O4=75∶2.5∶1时,TPTF的催化活性最佳;P25、纯TiO2、TPTF(nTiO2∶n噻吩单体:nFe3O4=75∶2.5∶1)和TiO2/Fe3O4(TF)光催化降解苯酚的速率常数分别是0.0371、0.0302、0.0253和0.0106 min-1;TPTF循环使用5次,其反应速率常数、饱和磁化强度以及磁回收率为0.0205 min-1、1.59emu/g和89.3%,比第1次的0.0253 min-1、1.85 emu/g和94.7%略有降低。