超声波辅助提取雨水管道沉积物中磷的存在形态

在SMT法的基础上采用超声波技术对实验条件进行优化,用于雨水管道沉积物中磷的提取。通过对提取时间、提取温度等影响提取效率的因素进行分析,确定了提高闭蓄态磷提取效率的条件,从而建立了管道沉积物中磷形态分析的最佳条件。在确定的最佳提取条件下对北京城区雨水管道内沉积物中磷的存在形态进行提取,并对不同形态磷的污染水平和分布状况进行分析,结合环境状况等因素对不同形态磷的污染特性进行了综合研究。     

土壤溶解性有机质荧光特征及其与铜的络合能力

选取4种不同类型土壤和腐熟鸡粪,透析提取溶解性有机质(DOM),通过凝胶色谱、三维荧光光谱测定并分析了DOM的相对分子质量(M_r)分布、化学结构特征及其与铜的结合能力.结果表明,鸡粪DOM相对分子质量积分面积远高于其他样品,表现出其具有较高的有机物含量,泥炭土次之.暗棕壤、褐土和黑土较低,仅为鸡粪积分面积的4.5%~5%.鸡粪在中分子量段积分面积约占总物质的34.1%,低分子量段和高分子量段分别约占41.7%和24.2%.荧光光谱分析表明,各样品均出现类蛋白荧光峰(E_x/E_m=240~270/300~350 nm),在中、高分子量段(M_r500)暗棕壤存在的荧光峰消失.泥炭土出现了较为独特的可见光区类富里酸荧光峰(E_x/E_m=325/420 nm),该荧光峰和黑土的荧光峰在中、高分子量段(M_r500)都产生了红移现象.鸡粪分别出现了和黑土类似的紫外区类富里酸荧光峰,以及和泥炭土类似的可见光区类富里酸荧光峰,以及一类独特的类蛋白荧光峰(E_x/E_m=280/350 nm),但这种类蛋白荧光峰在中分子量段(500M_r12 000)消失.分析表明泥炭土与Cu的络合常数(lg K)为4.13,其他3种土壤与Cu的络合常数较小且差别不大,集中在2.10~3.10之间.鸡粪与Cu的结合能力最大,络合常数达到6.66.     

大型铜尾矿库区节节草(Hippochaete ramosissimum)根际土壤重金属形态分布与影响因素研究

通过野外调查和实验分析,对安徽省铜陵市铜官山铜尾矿库、狮子山铜尾矿库及狮子山铜尾矿库周边农田3处生长的节节草根际与非根际土壤中重金属(Cu、Cd、Pb、Zn)的形态、含量和分布进行了研究.结果表明,节节草根际与非根际土壤重金属的主要形态分布基本一致,均表现为矿物态含量占据了重金属全量的大部分,而交换态含量偏低.与非根际土壤相比较,根际土壤中交换态、有机态重金属所占比例显著增加,其中Cu的有机结合态所占比例增加了53 25%、Cd、Pb的有机结合态所占比例增加超过17%,Zn则增加了5.67%;与此同时,碳酸盐结合态和铁锰氧化物结合态含量有所下降.统计分析表明,Cu、Cd、Pb、Zn在根际土壤中的形态分布与土壤pH值、有机质含量、植物生长等因素密切相关.     

太湖东北部沉积物理化特征及磷赋存形态研究

对太湖东部和北部8个沉积物样品进行了理化性质及磷赋存形态分析,在此基础上探讨了沉积物各理化性质与磷赋存形态间的相关关系。研究结果表明：太湖沉积物的总磷含量为307.43～1454.39 mg/kg,阳离子交换量为15.18～22.68 meq/100g土,有机质含量为1.66%～3.45%;颗粒组成以粉砂级和粘粒级为主,占总量的54.39%～76.83%;主要矿物组成为石英和长石,粘土矿物以伊利石/蒙脱石混层为主,其次是伊利石、绿泥石和高岭石;沉积物中氧化物以SiO2、Al2O3和TFe2O3为主,且它们的含量随沉积物中总磷含量的不同变化较大。磷的形态以无机磷为主,污染较重沉积物中铁/铝磷的含量明显升高,有机磷的比例降低,钙磷变化不大。沉积物的各理化性质与磷赋存形态间关系密切,随着沉积物中总磷含量的增加, 阳离子交换量和有机质的含量都逐渐升高,细颗粒含量（<2 μm）逐渐增多,铁/铝形态的磷在总磷中所占比例也逐渐增大。     

高原浅水湖泊沉积物中磷、氮形态化学研究

以滇池马村湾和海东湾为研究对象,对其沉积物－间隙水－上覆水三界面中的磷、氮形态作研究,其中钙结合态磷占的比例最大,其次是有机/细菌聚合态磷和残渣磷;总氮含量很高,平均值为2.63 mg/g,而亚硝酸盐氮含量很低,其它三种无机氮形态（硝酸盐氮、亚硝酸盐氮和氨氮）之间并不存在恒定的化学计量关系,这主要是无机氮循环还受水体和沉积物中有机氮的影响。调查还表明沉积物中Fe P含量与间隙水中溶解性磷酸盐磷有着较好的线性关系,沉积物中Fe P含量与间隙水Eh呈对数关系。     

Ecogenetic features and functions of solods in transural forest-steppes (within Sverdlovsk Oblast)

Specific ecogenetic features of solods in the forest-steppe zone has been studied, and the role of biotic and abiotic factors of soil formation has been estimated. Differentiation of soil horizons with respect to the physical clay fraction accounts for specific features of their moistening, which is reflected in the ratio of strongly and weakly crystallized forms of iron. Periodic changes in redox conditions results in iron segregation, and a high content of fulvic acids accounts for its eluvial migration. These processes are controlled by soil geochemical barriers.     

添加天然沸石和石灰对土壤镉形态转化的影响

采用土壤培养实验,研究镉污染土壤中添加沸石、石灰及两者配施对土壤pH值和土壤镉形态变化的影响。结果表明,土壤pH值随沸石用量的增加而增加,随培养时间呈现先增加后下降并逐渐趋于稳定的趋势,但均高于对照。高剂量石灰的处理对土壤pH的影响最大,与对照相比土壤pH提高了3.33个单位。在土壤5~50 d培养过程中,石灰处理的土壤交换态镉含量呈现先逐渐降低而后略有升高的趋势,其余处理均呈下降趋势。培养50 d后,高剂量的沸石、石灰及高剂量沸石与石灰配施处理的土壤交换态镉含量从5 d时的67.54、61.95和55.56 mg/kg降低至54.65、49.93和45.96mg/kg。相关分析表明,不同培养时期交换态镉含量与土壤pH值呈负相关关系。在10个处理中,L2Z3(石灰2 g/kg土和沸石60 g/kg土)组合处理效果最好,使土壤交换态镉含量下降了34.68%,碳酸盐结合态镉含量上升了4.30%,铁锰氧化结合态镉含量上升了16.97%,有机结合态镉含量上升了1.31%,残渣态镉含量上升了12.11%。     

Improved xenobiotic-degrading activity of Rhodococcus opacus strain 1cp after dormancy

The goals of the present work were as follows: to obtain the dormant forms of R. opacus 1cp; to study the phenotypic variability during their germination; to compare phenotypic variants during the growth on selective and elective media; and to reveal changes in the ability of the strain to destruct xenobiotics that had not been degradable before dormancy. It was shown that Rhodococcus opacus 1cp (the strain degrading chlorinated phenols) became able to utilize a broader spectrum of xenobiotics after storage in the dormant state. Germination of the dormant forms of R. opacus 1cp on an agarized medium was followed by emergence and development of phenotypic variants that could grow on 4-chlorophenol and 2,4,6-trichlorophenol without adaptation. The cells of R. opacus 1cp phenotypic variants also utilized all of the tested chlorinated phenols: 2,3-, 2,5-, and 2,6-dichloro-, 2,3,4- and 2,4,5-trichloro-, pentachlorophenol, and 1,2,4,5-tetrachlorobenzene in concentrations up to 60 mg/L, though at the lower rates than 4-CP and 2,4,6-TCP. The improved degradation of chlorinated phenols by R. opacus strain 1cp exposed to the growth arrest conditions demonstrates the significance of dormancy for further manifestation of the adaptive potential of populations. A new principle of selection of variants with improved biodegradative properties was proposed. It embraces introduction of the dormancy stage into the cell life cycle with subsequent direct inoculation of morphologically different colonies into the media with different toxicants, including those previously not degraded by the strain.     

三垟湿地沉积物-间隙水-上覆水界面磷形态研究

沉积物与上覆水间营养物质交换,成为导致水体发生富营养化的首要化学变迁过程.分别在三垟湿地的柑橘林(S1)、景观用地(S2)和生活用地(S3)取样,研究了沉积物-间隙水-上覆水界面磷形态以及相互关系.结果表明:(1)沉积物TP增加时,间隙水PO3-4和可溶性总磷(TDP)也增加.要削减磷在上覆水中的含量,控制间隙水PO3-4或TDP是一良策.(2)随着沉积物铁磷、铝磷的增加,间隙水PO3-4也增加.在三垟湿地沉积物中,铁磷和铝磷含量都可作为间隙水PO34-含量的指示.(3)S1、S2和S3的沉积物活性磷、间隙水TDP和上覆水TDP存在明显的浓度梯度,沉积物活性磷＞间隙水TDP＞上覆水TDP.说明在三垟湿地中,沉积物活性磷是磷释放的关键因子,而沉积物-间隙水界面则是磷释放的关键界面.     

Quantification of the interactions between Ca,Hg and extracellular polymeric substances (EPS) of sludge

The interactions between metals (Ca²⁺ and Hg²⁺) and extracellular polymeric substances (EPS) extracted from the aerobic and anaerobic sludge in wastewater treatment reactors were investigated using a combination of zeta potential measurement and 3-dimensional excitation–emission matrix (EEM) fluorescence spectroscopy with parallel factor (PARAFAC) analysis. Results show that Ca²⁺ had no substantial effects on the EEM fluorescence spectra of the EPS, but their zeta potentials increased with the increasing Ca²⁺ dosage. However, Hg²⁺ had a significant effect on the EEM fluorescence spectra of the EPS, while their zeta potentials seemed not to be affected by the dose of Hg²⁺. The interactions between Hg²⁺ and EPS were elucidated using the fluorescence quenching with PARAFAC analysis, while the interactions between Ca²⁺ and EPS were evaluated by the zeta potential technique. The binding constants for Hg²⁺ and EPS were two orders of magnitude higher than those for Ca²⁺ and EPS, suggesting that the binding mechanisms between Ca²⁺ and EPS were different from those between Hg²⁺ and EPS. The results might be useful for understanding the roles of EPS in bacterial self-protection against heavy metals and the aggregate formation mechanisms through ionic bridging interactions.