土壤颗粒对纳米TiO_2悬浮稳定性作用机制的实验研究

在不含表面活性剂和含有表面活性剂两种条件下,研究了土壤颗粒对纳米TiO2(nTiO2)悬浮稳定性的影响.结果表明,土壤颗粒降低了nTiO2在水相中的悬浮稳定性.当体系中不含表面活性剂时,nTiO2在土壤大颗粒上的沉积是导致nTiO2脱稳沉淀的主要原因.在含有表面活性剂的溶液中,土壤颗粒降低nTiO2悬浮稳定性的作用变得更加明显了.一方面,表面活性剂加速了土壤颗粒本身的沉降从而增强了nTiO2在其中的沉降,另一方面,表面活性剂在土壤上的强烈吸附促进了表面活性剂-nTiO2在土壤上的沉积.扫描电镜显示,nTiO2不仅吸附在土壤大颗粒上,还会吸附在土壤小颗粒表面.3种表面活性剂中,十六烷基三甲基溴化铵(CTAB)悬浮的nTiO2与土壤颗粒共沉淀现象最明显.除了土壤对CTAB的吸附作用之外,XDLVO/DLVO能量计算显示CTAB体系中土壤颗粒与nTiO2之间存在显著第二极小值,表明nTiO2能够在第二极小值位置与土壤颗粒结合,从而与土壤颗粒一起快速沉淀.     

磺胺类抗生素在斑马鱼体内的生物富集性及模型预测评估

针对磺胺类抗生素在鱼体内的生物富集特性,采用半静态生物富集测试法,研究磺胺二甲嘧啶(SMT)和磺胺甲恶唑(SMX)在斑马鱼(Brachydanio rerio)体内的生物富集规律及生物富集系数(bio-concentration factor,BCF),并选用3种常用预测模型对2种磺胺类抗生素的BCF值进行估算,比较了估算值与实际测定值,为磺胺类抗生素生物富集性的预测提供依据。研究结果表明,当暴露浓度为0.01 mg·L~(-1)~1.00 mg·L~(-1)时,鱼体对SMT的最大生物富集系数BCF值为1.11,最大富集量出现在暴露24~48 h期间;SMX的最大BCF值为1.15,最大富集量处于暴露96~168 h之间。根据磺胺类抗生素的理化性质,通过比较3种生物富集预测模型获得SMT和SMX的BCF值,发现其中Kow预测模型所得估算值最为接近实测值。因此可利用该模型作为磺胺类抗生素富集性的预测工具,为我国兽药抗生素的环境风险预测和评价提供依据。     

预测沉积物-水微宇宙系统中化学品浓度变化的多介质模型

沉积物-水微宇宙系统是经济合作发展组织(Organisation for Economic Co-Operation and Development,OECD)颁布的化学品测试准则中推荐的试验系统之一,可用来测试化学品对底栖生物的慢性毒性。为了在试验前对化学品的浓度变化进行预测,进而确定试验方法,以摇蚊慢性毒性试验系统为例,采用环境多介质模型的建模方法,构建了一种可通过化学品理化性质和试验系统参数,对化学品在沉积物-水试验系统中浓度变化进行预测的模型。结合试验数据和文献资料,给出了模型中试验系统参数的推荐取值,并使用Matlab软件中的Simulink工具对模型进行编程和求解。以此模型为基础,给出了模型在3个方面的应用,即预测蓄积时间、预测平衡时间以及拟合试验数据。对80种已有或假想化学品的蓄积时间和平衡时间进行了计算,得出的范围分别为1~204 d和1~73 d。此外,适当修改模型结构和模型参数,也可将其应用于其他暴露场景中。但使用模型对化学品浓度进行预测时发现,模型仅对沉积物中化学品浓度的预测结果较为准确,而对水中化学品浓度的预测结果与实测值相差1~2个数量级。模型对浓度的预测精度未来仍需进一步提高。上述研究结果完善了沉积物-水微宇宙系统试验方法。     

表观遗传学机制与空气污染的健康效应

空气污染是一个全球性的问题,并且具有深远的环境影响。暴露于空气污染会对人体健康产生许多不同的影响,理解空气污染的健康效应又是一个复杂命题,既要考虑不同类型的污染物同时也要考虑相关疾病的复杂性。然而越来越多的研究表明,表观遗传学在空气污染相关疾病的发生、发展中发挥着重要的作用。空气污染物可引起DNA甲基化、组蛋白修饰和miRNA表达等表观遗传学改变,这种改变往往发生在疾病产生的早期,因此相关研究不仅可以了解疾病的发病机制,而且还为疾病早期诊断和预防筛选可能的标志物。本文综述了表观遗传学的几种修饰方式和空气污染物造成不良健康损伤机制的一些研究进展。     

华西雨屏区典型人工林对降雨过程中NH_4~+-N和NO_3~--N的过滤作用

氮沉降已成为河流、湖泊及城市等生态系统的主要污染威胁因素之一,森林生态系统能从林冠、地被和土壤自上而下截留过滤大气降雨中的NH+4-N和NO-3-N,是区域大气环境污染生态防治的重要途径.选取华西雨屏区几种典型人工林森林生态系统为研究对象,采用定位监测与室内分析相结合的研究方法,于2011年4—12月对大气降水、穿透雨、树干茎流、地表径流和地下渗滤NH+4-N和NO-3-N的含量与分配进行了研究.结果表明:观测期内40次降雨总雨量为492.72 mm,NH+4-N和NO-3-N的总沉降量分别为13.248 kg·hm-2和16.320 kg·hm-2;3种人工林林冠层对NH+4-N和NO-3-N的过滤能力表现为香樟林混交林柳杉林,而地表和土壤层均表现为混交林香樟林柳杉林;无林地、香樟林、柳杉林和混交林生态系统无机氮截留过滤净输入量分别为19.557、44.079、42.331、64.896 kg·hm-2,对无机氮的综合过滤作用表现为混交林香樟林柳杉林无林地.这些结果说明华西雨屏区合理配置混交林能更加有效地降低大气氮沉降对生态系统的影响.     

烧结机共处置危险废物过程中重金属Pb、Zn的挥发特性

利用化学试剂PbCl2、ZnCl2来模拟危险废物,研究了烧结机共处置危险废物过程中Pb、Zn的挥发特性.首先选取PbCl2、ZnCl2两种化合物的纯化学试剂分别进行了热重分析实验,然后对掺有一定比例PbCl2、ZnCl2的烧结矿原料进行煅烧,采集分析煅烧烟气和煅烧所得烧结矿中Pb和Zn的总量.实验结果表明,在刚开始煅烧的一段时间内,Pb、Zn两种重金属挥发特性相似,均是随着时间的增加以及温度的升高而挥发率逐渐上升,而当煅烧超过一定时间后,其挥发和固化反应会达到平衡,当煅烧的温度为1200℃时,Pb和Zn的挥发率分别为97.13%和65.04%.运用化学反应动力学理论对Pb、Zn两种重金属在烧结机共处置过程中的挥发规律进行动力学模拟,模拟结果表明,PbCl2中Pb挥发的动力学方程可表示为α=f(T,t)=1-exp[-7.90exp(-5595/T)t];而ZnCl2中的Zn为α=f(T,t)=1-exp[-0.534exp(-3210/T)t].     

Impact of dissolved organic matter on the photolysis of the ionizable antibiotic norfloxacin

Norfloxacin (NOR), an ionizable antibiotic frequently used in the aquaculture industry, has aroused public concern due to its persistence, bacterial resistance, and environmental ubiquity. Therefore, we investigated the photolysis of different species of NOR and the impact of a ubiquitous component of natural water — dissolved organic matter (DOM), which has a special photochemical activity and normally acts as a sensitizer or inhibiter in the photolysis of diverse organics; furthermore, scavenging experiments combined with electron paramagnetic resonance (EPR) were performed to evaluate the transformation of NOR in water. The results demonstated that NOR underwent direct photolysis and self-sensitized photolysis via hydroxyl radical (·OH) and singlet oxygen (¹O₂) based on the scavenging experiments. In addition, DOM was found to influence the photolysis of different NOR species, and its impact was related to the concentration of DOM and type of NOR species. Photolysis of cationic NOR was photosensitized by DOM at low concentration, while zwitterionic and anionic NOR were photoinhibited by DOM, where quenching of UOH predominated according to EPR experiments, accompanied by possible participation of excited triplet-state NOR and ¹O₂. Photo-intermediate identification of different NOR species in solutions with/without DOM indicated that NOR underwent different photodegradation pathways including dechlorination, cleavage of the piperazine side chain and photooxidation, and DOM had little impact on the distribution but influenced the concentration evolution of photolysis intermediates. The results implied that for accurate ecological risk assessment of emerging ionizable pollutants, the impact of DOM on the environmental photochemical behavior of all dissociated species should not be ignored.     

Enhanced bio-decolorization of 1-amino-4-bromoanthraquinone-2-sulfonic acid by Sphingomonas xenophaga with nutrient amendment

Bacterial decolorization of anthraquinone dye intermediates is a slow process under aerobic conditions. To speed up the process, in the present study, effects of various nutrients on 1-amino-4-bromoanthraquinone-2-sulfonic acid (ABAS) decolorization by Sphingomonas xenophaga QYY were investigated. The results showed that peptone, yeast extract and casamino acid amendments promoted ABAS bio-decolorization. In particular, the addition of peptone and casamino acids could improve the decolorization activity of strain QYY. Further experiments showed that L-proline had a more significant accelerating effect on ABAS decolorization compared with other amino acids. L-Proline not only supported cell growth, but also significantly increased the decolorization activity of strain QYY. Membrane proteins of strain QYY exhibited ABAS decolorization activities in the presence of L-proline or reduced nicotinamide adenine dinucleotide, while this behavior was not observed in the presence of other amino acids. Moreover, the positive correlation between L-proline concentration and the decolorization activity of membrane proteins was observed, indicating that L-proline plays an important role in ABAS decolorization. The above findings provide us not only a novel insight into bacterial ABAS decolorization, but also an L-proline-supplemented bioaugmentation strategy for enhancing ABAS bio-decolorization.     

Growth and alkaline phosphatase activity of Chattonella marina and Heterosigma akashiwo in response to phosphorus limitation

The growth and alkaline phosphatase activity (APA) of two raphidophyceae species Chattonella marina and Heterosigma akashiwo were investigated in response to P-limitation and subsequent addition of dissolved inorganic phosphorus (DIP, NaH₂PO₄) and two dissolved organic phosphorus (DOP) compounds: guanosine 5-monophosphate (GMP) and triethyl phosphate (TEP). APAlevels increased greatly after P-starvation as the decrease of the cellular phosphorus quotes (Q_p). C. marina responded to P-limitation quickly and strongly, with 10-fold increase in APA within 24 hr after P-starvation. The larger difference between maximal and minimal Q_p values in C. marina indicated its high capacity in P storage. APA of H. akashiwo wasmaximally enlarged about 2.5 times at 48 hr of P-starvation. After the addition of nutrients, cell numbers of C. marina increased in all treatments including the P-free culture, demonstrating the higher endurance of C. marina to P-limitation. However, those of H. akashiwo increased only in DIP and GMP cultures. APA increased only after the addition of the monophosphate ester GMP. The results suggest that quick responses of C. marina to P-limitation, high capacity in P storage as well as endurance for P-depletion provide this species an ecological advantage in phytoplankton community competition under DIP-limited conditions.     

Heterogeneous oxidation of SO2 by O3-aged black carbon and its dithiothreitol oxidative potential

Ozone (O₃) is an important atmospheric oxidant. Black carbon (BC) particles released into the atmosphere undergo an aging process via O₃ oxidation. O₃-aged BC particles may change their uptake ability toward trace reducing gases such as SO₂ in the atmosphere, leading to different environmental and health effects. In this paper, the heterogeneous reaction process between O₃-aged BC and SO₂ was explored via in-situ diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS). Combined with ion chromatography (IC), DRIFTS was used to qualitatively and quantitatively analyze the sulfate product. The results showed that O₃-aged BC had stronger SO₂ oxidation ability than fresh BC, and the reactive species/sites generated on the surface had an important role in the oxidation of SO₂. Relative humidity or 254 nm UV (ultraviolet) light illumination enhanced the oxidation uptake of SO₂ on O₃-aged BC. The oxidation potentials of the BC particles were detected via dithiothreitol (DTT) assay. The DTT activity over BC was decreased in the process of SO₂ reduction, with the consumption of oxidative active sites.