草甸棕壤中镉、铅、油含量对微生物类群和生化活性的影响

本研究以重金属化合物(CdCl_2、PbCl_2)和矿物油作为土壤的污染物,分析土壤中镉、铅、油的含量对土壤微生物类群与生化活性的影响。结果表明,镉、铅、油对水旱田中的细菌抑制作用比较明显,对放线菌、真菌抑制作用较差。小剂量的镉、铅、油对固氮菌有刺激作用,大剂量则有抑制作用。对尿酶和硝化细菌的代谢有明显抑制作用,对其它酶类不明显。 从含重金属的平板培养基上反映出土壤对重金属的掩蔽作用。污染物对微生物的生化活性的临界毒害浓度分别为:镉 5—60ppm;铅 300—500ppm;油 500—5000ppm。     

丹东市区段鸭绿江水体中铅、镉的含量

利用生物指示物（鳙鱼）对丹东地区鸭绿江水体中的铅、镉污染进行监测，采具鳙鱼-碳化酸溶-电热原子光谱法对丹东鸭绿江流域鳙鱼体内的铅、镉的含量进行了相关检测，在相同的实验条件下对该地区的水体中的铅、镉的含量进行对比，并对该地区的铅、镉污染进行了相关的评价，通过一年的监测未见超标。铅、镉含量分别为6．53±0．07（ng/g）、4．60±0．03（ng/g）；回收率分别为98.9％、103.5％；RSD分别为5．3％、4．1％。     

半固态培养条件下烟曲霉去除土壤中镉

选用了1株高耐镉(Cd)的烟曲霉,提出了利用烟曲霉在半固态培养体系表面生长并去除Cd的方法,研究了菌体对不同模拟Cd污染水平土壤中Cd的去除效果,测定了菌体吸附和富集Cd的变化.结果表明,烟曲霉在半固态培养体系中能够实现一定的Cd去除效果,Cd含量为10 mg·kg~(-1)时,对土壤Cd的综合去除率可达31%.同时通过研究不同Cd含量下烟曲霉干重和体系pH随时间变化情况,发现随着培养时间和Cd含量的增加,烟曲霉干重逐渐下降,最大下降幅度可达64%,pH为5.6~6.0时去除效果较好.培养过程中土壤Cd形态变化表明,烟曲霉在该体系下主要去除土壤中弱酸溶态和可还原态的Cd,可氧化态Cd含量在培养前后基本保持不变.这种方法的提出为微生物去除土壤重金属污染提供了新的思路.     

外源钙盐对盐胁迫下沙拐枣渗透调节和膜脂过氧化的影响

为了解外源钙对缓解沙拐枣（Calligonum mongolicum）盐胁迫的主要生理机制,采用盆栽法探究在0、100、200 mmol/L的NaCl胁迫下,分别添加5、10、15和20 mmol/L的Ca（NO₃）₂对沙拐枣同化枝中w（脯氨酸）、丙二醛含量、w（可溶性蛋白）、w（可溶性糖）的影响.结果表明,单独添加Ca（NO₃）₂使沙拐枣同化枝内w（脯氨酸）、丙二醛含量、w（可溶性蛋白）以及w（可溶性糖）增加,即Ca（NO₃）₂对沙拐枣的生长造成了胁迫.对w（脯氨酸）、丙二醛含量、w（可溶性蛋白）、w（可溶性糖）来说,NaCl和Ca（NO₃）₂之间均存在极显著的交互作用,与对照相比,在c（NaCl）分别为100、200 mmol/L,添加c[Ca（NO₃）₂]为10、20 mmol/L时,w（脯氨酸）显著增加,分别达到最大值（736.7、1 086.3 μg/g）;丙二醛含量分别降低了37.8%和40.5%,w（可溶性蛋白）以及w（可溶性糖）均增加.总之,适宜浓度的钙盐通过增加渗透物质w（脯氨酸）、w（可溶性蛋白）及w（可溶性糖）,降低丙二醛的含量来有效缓解盐胁迫对沙拐枣幼苗产生的伤害,当c（NaCl）/c[Ca（NO₃）₂]为10:1时,缓解作用最佳,并且钙盐对沙拐枣盐胁迫的缓解属于抗性诱导的调节作用.      

外源水溶性氟在茶园土壤中赋存形态的转化及其生物有效性

采用盆栽实验和化学连续提取法,研究了外源添加水溶性氟在茶园土壤中的赋存形态转化及不同赋存形态氟对茶树氟富集的贡献.结果表明,茶园土壤中本底各赋存形态氟含量随时间的变异很小,处于相对稳定状态,外源水溶性氟进入土壤后迅速向各个形态转化,10 mg·kg-1氟处理下,水溶性氟含量表现为先升后降的趋势,有机束缚态氟和铁锰结合态氟含量随着处理时间呈下降的趋势,可交换态氟含量处理前后含量没有显著性差异(P>0.05),残余态氟含量则保持相对稳定的状态;200mg·kg-1氟处理下,水溶性氟、铁锰结合态氟和有机束缚态氟含量随着处理时间呈下降的趋势,可交换态氟含量则表现为先升后降的趋势,处理前后含量没有显著性差异(P>0.05),残余态氟含量则为上升的趋势,与10 mg·kg-1氟处理表现有差异.0~10 mg·kg-1氟处理内,茶树根、茎和叶中总氟含量之间的差异达显著水平(P<0.05);在10~100 mg·kg-1氟处理内,则变化不显著(P>0.05).逐步回归分析表明茶园土壤中不同氟形态对茶树根、茎和叶中水溶性氟和总氟的积累贡献有差异,叶片总氟含量与土壤中水溶性氟、铁锰结合态氟、有机束缚态氟和残渣态氟含量有显著的回归关系(P<0.05),而叶片水溶性氟含量与土壤各赋存形态氟含量没有显著的回归关系(P>0.05).     

嗜麦芽窄食单胞菌对铜镉的吸附特性与离子交换

研究了投菌量、金属浓度和戊二醛浓度对嗜麦芽窄食单胞菌吸附水体中Cu2+和Cd2+特性的影响,分析了重金属生物吸附、NO3-去除与菌体离子释放的关联,从离子吸附、交换、转化与释放的角度探讨了重金属生物吸附机制.结果表明嗜麦芽窄食单胞菌对Cu2+和Cd2+吸附性能良好,0.2 g·L-1干重菌体处理浓度为0.05 mmol·L-1的Cu(NO3)2和Cd(NO3)2溶液120 min后,Cu2+和Cd2+的吸附率分别达96.3%和83.9%.菌体对Cu(NO3)2和Cd(NO3)2溶液的吸附过程存在Cu2+和Cd2+的表面吸附与胞内运输、NO3-胞内积累、NO3-还原为NO2-等行为,而且Cu2+和Cd2+的胞内运输、NO3-积累和还原需要消耗能量,并会促进Cl-、PO43-、SO42-、Na+、NH4+、K+和Ca2+等离子的释放.红外光谱分析表明菌体酰胺基、羟基与羧基均参与了Cu2+和Cd2+的吸附.X-光电子能谱分析显示吸附后Cu2+和Cd2+的价态不发生变化.     

Phytoremediation potential of charophytes: Bioaccumulation and toxicity studies of cadmium, lead and zinc

The ability for usage of common freshwater charophytes,Chara aculeolata and Nitella opaca in removal of cadmium (Cd),lead (Pb) and zinc (Zn) from wastewater was examined.C.aculeolata and N.opaca were exposed to various concentrations of Cd (0.25 and 0.5 mg/L),Pb (5 and 10 mg/L) and Zn (5 and 10 mg/L) solutions under hydroponic conditions for 6 days.C.aculeolata was more tolerant of Cd and Pb than N.opaca.The relative growth rate of N.opaca was drastically reduced at high concentrations of Cd and Pb although both were tolerant of Zn.Both macroalgae showed a reduction in chloroplast,chlorophyll and carotenoid content after Cd and Pb exposure,while Zn exposure had little effects.The bioaccumulation of both Cd and Pb was higher in N.opaca (1544.3 μg/g at 0.5 mg/L Cd,21657.0 μg/g at 10 mg/L Pb) whereas higher Zn accumulation was observed in C.aculeolata (6703.5 μg/g at 10 mg/L Zn).In addition,high bioconcentration factor values (> 1000) for Cd and Pb were observed in both species.C.aculeolata showed higher percentage of Cd and Pb removal (> 95%) than N.opaca and seemed to be a better choice for Cd and Pb removal from wastewater due to its tolerance to these metals.     

Removal of Cd2+ from water by Friedel’s salt (FS: 3CaO.Al2O3·CaCl2·10H2O): Sorption characteristics and mechanisms

The development of low-cost and efficient new mineral adsorbents has been a hot topic in recent years. In this study, Friedel’s salt (FS:3CaO·A12O3 ·CaCl2 ·10H2O), a hexagonal layered inorganic absorbent, was synthesized to remove Cd2+ from water. The adsorption process was simulated by Langmuir and Freundlich models. The adsorption mechanism was further analyzed with TEM, XRD, FT-IR analysis and monitoring of metal cations released and solution pH variation. The results indicated the adsorbent FS had an outstanding ability for Cd(Ⅱ) adsorption. The maximum adsorption capacity of the FS for Cd(Ⅱ) removal can reach up to 671.14 mg/g. The nearly equal numbers of Cd2+ adsorbed and Ca2+ released demonstrated that ion-exchange (both surface and inner) of the FS for Cd(Ⅱ) played an important role during the adsorption process. Furthermore, the surface of the FS after adsorption was microscopically disintegrated while the inner lamellar structure was almost unchanged. The behavior of Cd(Ⅱ) adsorption by FS was significantly affected by surface reactions. The mechanisms of Cd2+ adsorption by the FS mainly included surface complexation and surface precipitation. In the present study, the adsorption process was fitted better by the Langmuir isotherm model (R2 = 0.9999) than the Freundlich isotherm model (R2 = 0.8122). Finally, due to the high capacity for ion-exchange on the FS surface, FS is a promising layered inorganic adsorbent for the removal of Cd(Ⅱ) from water.     

Simultaneous preconcentration of cadmium and lead in water samples with silica gel and determination by flame atomic absorption spectrometry

A new method that utilizes pretreated silica gel as an adsorbent has been developed for simultaneous preconcentration of trace Cd(II) and Pb(II) prior to the measurement by flame atomic absorption spectrometry. The effects of pH, the shaking time, the elution condition and the coexisting ions on the separation/preconcentration conditions of analytes were investigated. Under optimized conditions, the static adsorption capacity of Cd(II) and Pb(II) were 45.5 and 27.1mg/g, the relative standard deviations were 3.2% and 1.7% (for n = 11), and the limits of detection obtained were 4.25 and 0.60 ng/mL, respectively. The method was validated by analyzing the certified reference materials GBW 07304a (stream sediment) and successfully applied to the analysis of various treated wastewater samples with satisfactory results.     

运用丝状真菌生物质生物吸附镉(Ⅱ)污染物的研究

丝状真菌生物质是研制可用作生物修复镉污染的生物吸附剂的重要生物材料。文章首先概述了镉的危害性与镉污染的真菌修复机制;列表比较了近20年研究中用于生物吸附Cd⁽²⁺⁾的丝状真菌菌种资源、镉吸附量和工艺特性参数;详细阐明了利用丝状真菌生物质生物吸附法除镉工艺过程涉及的技术方法和基本原理,包括丝状真菌生物质材料的预处理方法,分批生物吸附除镉工艺的考虑因素及其影响效应,固定床吸附柱生物吸附除镉工艺,以及生物吸附法去除含镉工业废水中Cd(2+)的丝状真菌菌种资源、镉吸附量和工艺特性参数;详细阐明了利用丝状真菌生物质生物吸附法除镉工艺过程涉及的技术方法和基本原理,包括丝状真菌生物质材料的预处理方法,分批生物吸附除镉工艺的考虑因素及其影响效应,固定床吸附柱生物吸附除镉工艺,以及生物吸附法去除含镉工业废水中Cd⁽²⁺⁾的实践效果。