改性当地土壤湖泊综合修复技术对浮游植物群落变动的影响

采用改性当地土壤湖泊综合修复技术从2008年夏季到2010年夏季连续在太湖十八湾围隔内实施夏季应急除藻工程和春季底泥调控工程,通过连续监测浮游植物的群落变动发现:在2009年,春季和夏季工程后浮游植物门类虽在短时间内减少,但是一个月内均又恢复,而且春季工程在短时间内可以在一定程度上抑制蓝藻的种类和比例的增加,又可提高硅藻和绿藻的种类和比例,这对于春季沉水植被的恢复和抑制蓝藻的复苏都有积极意义;从长时间周年变化来看,春季和夏季工程在围隔内连续实施2年,蓝藻水华暴发周期和暴发规模均呈逐渐缩短趋势。这对于进一步开展蓝藻复苏和蓝藻水华暴发的机理研究和控制技术的研究都有一定的指导意义。     

太湖十八湾嗅味物质变化规律及除嗅方法

为了探索湖泊水体中嗅味物质的变化规律,解决湖泊水体的嗅味问题,本研究选取太湖十八湾围隔水域作为调查对象,从2009年12月到2010年8月,对嗅味物质土臭素(geosmin)和二甲基异茨醇(MIB)的含量进行分析检测,结果表明,geosmin的含量和MIB的含量在冬春季节较低,夏秋季节较高,随季节波动明显,MIB是主要的致嗅物质。为调控臭氧稳定性,降低臭氧衰减速率,室内实验采用硅藻土来吸附夹载臭氧,使臭氧分解速率常数由0.036/min降低到了0.015/min,由此制得了臭氧-硅藻土,并用该材料处理模拟嗅味物质水样。结果表明,10 min时,geosmin和MIB的去除率分别为73.4%和46.6%,高于对照中的45.9%和20.5%,30 min时,geosmin和MIB的去除率进一步提高到96.1%和79.7%,本研究结果为解决湖泊等天然水体的嗅味问题提供了新的思路。     

Cr(VI) uptake mechanism of Bacillus cereus

In this study, we investigated the Cr(VI) uptake mechanism in an indigenous Cr(VI)-tolerant bacterial strain -Bacillus cereus through batch and microscopic experiments. We found that both the cells and the supernatant collected from B. cereus cultivation could reduce Cr(VI). The valence state analysis revealed the complete transformation from Cr(VI) into Cr(III) by living B. cereus. Further X-ray absorption fine structure and Fourier transform infrared analyses showed that the reduced Cr(III) was coordinated with carboxyl and amido functional groups from either the cells or supernatant. Scanning electron microscopy and atomic force microscopy observation showed that noticeable Cr(III) precipitates were accumulated on bacterial surfaces. However, Cr(III) could also be detected in bacterial inner portions by using transmission electron microscopy thin section analysis coupled with energy dispersive X-ray spectroscopy. Through quantitative analysis of chromium distribution, we determined the binding ratio of Cr(III) in supernatant, cell debris and cytoplasm as 22%, 54% and 24%, respectively. Finally, we further discussed the role of bacterium-origin soluble organic molecules to the remediation of Cr(VI) pollutants.     

Source attribution for mercury deposition in the contiguous United States: regional difference and seasonal variation

Quantifying the contribution of emission sources responsible for mercury deposition in specific receptor regions helps develop emission control strategies that alleviate the impact on ecosystem and human health. In light of the maximum available control technology (MACT) rules proposed by U.S. Environmental Protection Agency (EPA) and the ongoing intergovernmental negotiation coordinated by United Nations Environmental Programme (UNEP) for mercury, the Community Multiscale Air Quality Modeling System (CMAQ-Hg) was applied to estimate the source contribution in six subregions of the contiguous United States (CONUS). The considered source categories include electric generating units (EGU), iron and steel industry (IRST), other industrial point sources excluding EGU and IRST (OIPM), the remaining anthropogenic sources (RA), natural processes (NAT), and out-of-boundary transport (BC). It is found that, on an annual basis, dry deposition accounts for two-thirds of total annual deposition in CONUS (474 Mg yr(-1)), mainly contributed by reactive gaseous mercury (about 60% of total deposition). The contribution from large point sources can be as high as 75% near the emission sources (< 100 km), indicating that emission reduction may result in direct deposition decrease near the source locations. Out-of-boundary transport contributes from 68% (Northeast) to 91% (West Central) of total deposition. Excluding the contribution from out-of boundary transport, EGU contributes to about 50% of deposition in the Northeast, Southeast, and East Central regions, whereas emissions from natural processes are more important in the Pacific and West Central regions (contributing up to 40% of deposition). This suggests that the implementation of the new EPA MACT standards will significantly benefit only these three regions. Emission speciation is a key factor for local deposition. The source contribution exhibits strong seasonal variation. Deposition is greater in warm seasons due to stronger Hg0 oxidation. However, the contribution from anthropogenic sources is smaller in warm seasons because of larger emissions from natural processes and stronger vertical mixing that facilitates transport.     

Acid neutralization of precipitation in Northern China

There is an increasing concern over the impact of human-related emissions on the acid precipitation in China. However, few measurements have been conducted so far to clarify the acid-neutralization of precipitation on a regional scale. Under a network of 10 sites across Northern China operated during a 3-year period from December 2007 to November 2010, a total of 1118 rain and snow samples were collected. Of this total, 28% was acid precipitation with pH < 5.6. Out of these acid samples, 53% were found heavily acidic with pH value below 5.0, indicating significantly high levels of acidification of precipitation. Most of the acidity of precipitation was caused by H2SO4 and HNO3, their relative contribution being 72% and 28%, respectively. However; the contribution of HNO3 to precipitation acidity will be enhanced due to the increasing NO(x) and stable SO2 emissions in future. Neutralization factors for K+, NH4+, Ca2+, Na+, and Mg2+ were estimated as 0.06, 0.71, 0.72, 0.15, and 0.13, respectively. The application of multiple regression analysis further quantified higher NH4+ and Ca2+ contribution to the neutralization process, but the dominant neutralizing agent varied from site to site. The neutralization was less pronounced in the rural than urban areas, probably due to different levels of alkaline species, which strongly buffered the acidity. Presence of high concentrations of basic ions was mainly responsible for high pH of precipitation with annual volume-weighted mean (VWM) values larger than 5.6 at several sites. It was estimated that in the absence of buffering ions, for the given concentration of SO4(2-) and NO3-, the annual VWM pH of precipitation would have been recorded around 3.5 across Northern China. This feature suggested that emissions of particles and gaseous NH3 played very important role in controlling the spatial variations of pH of precipitation in the target areas.     

超声波-缺氧／好氧污泥消化反应器中氨氧化细菌群落结构的演变

为了揭示超声波-缺氧／好氧污泥消化反应器中氨氧化细菌群落结构多样性的演变过程,采用变性梯度凝胶技术（PCR—DGGE）研究不同运行时期氨氧化细菌群落结构的变化。DGGE分析表明,反应器中氨氧化细菌群落比较丰富。在反应器运行的不同时期,氨氧化细菌的群落结构发生了一定的变化,反映了种群的动态演变。UPGMA聚类分析将DGGE图谱分为3大类群并对应于各自的运行时期。测序结果表明,反应器中的优势种群属于变形菌门（Proteobacteria）,包括α-proteobacteria,β-proteobacteria,γ-proteobacteria和ε-proteobacteria4个纲,其中β-proteobacteria占45％,γ-proteobacteria占40％。在始终保持明显优势地位的种属中,5株为反硝化细菌,它们对提高反应器脱氮效率具有重要作用。     

格宾护岸填料类型对河道自净能力的影响

选择花岗岩块石、卵石和废建筑砌块3种材料作为格宾填料,研究不同填料在模拟河道中对河水水质净化效果的影响。结果表明,随着实验装置运行时间的延长,各填料对N、P营养盐及有机物的去除能力均有不同程度的提高;3种填料中,卵石相较于其他2种填料对NH3-N、TOC和DOC的去除能力保持在较高的水平,运行26 d后分别达65.26%、71.06%和78.06%;3种填料在实验装置运行初期对TP都有较好的去除效果,运行12 d后,花岗岩块石、卵石、废建筑砌块对TP的去除率分别达89.20%、91.05%和94.71%;卵石表面附着的微生物脂磷含量及脱氢酶活性分别为53.43 nmol P/cm3、10.67μg TF/(h.cm3),均显著高于其他2种填料(p<0.05),其表面较高的微生物量及酶活性有利于对氮素及有机物的去除。     

聚合硫酸铁/高锰酸钾/二氧化氯组合工艺用于聚氯乙烯废水回收的工程化研究

采用聚合硫酸铁复配高锰酸钾混凝结合二氧化氯氧化的组合工艺成功解决了某厂聚氯乙烯生产废水回收工艺CODMn不达标问题。工程运行结果表明,当原水CODMn=30～48 mg/L,浊度=25～46 NTU时,在CFe=16.8 mg/L,CKMnO4=45 mg/L,CClO2=20 mg/L的条件下,出水CODMn<10 mg/L,浊度<0.5 NTU,达到工业循环补给水的水质要求。     

Concentrations of pentachlorophenol (PCP) in fish and shrimp in Jiangsu Province, China

Pentachlorophenol (PCP) concentrations were determined in 55 samples of fish, shrimp, crabs, frogs and turtles collected in Jiangsu Province and 55 freshwater shrimp samples collected from the Huiming Fish Market, Nanjing, China between 2003 and 2004. PCP concentrations ranged from less than the method detection limit (MDL: 0.5 microg/kg ww) to 61 microg/kg ww, with a mean of 5.2 microg/kg ww in 55 samples collected across Jiangsu Province and a mean of 0.5 microg/kg ww for freshwater shrimp collected from the Huiming Fish Market. Concentrations of PCP in common carp (Carassius auratus) were significantly greater than concentrations of PCP in other species from all of the areas studied. Grass carp (Ctenopharyngodon idella) contained the second greatest concentrations and crustacean species contained the least concentrations. Concentrations of PCP were greater in samples collected from Southern Jiangsu than those collected from other areas of Jiangsu Province. Concentrations of PCP in the freshwater shrimp (Macrobrachium nipponense) from the Huiming Fish Market were greater in March and September than those collected in June and December. Based on the allowable daily intake (ADI) set by the US National Academy of Science, current concentrations of PCP measured in aquatic products from Jiangsu Province presented minimus health risks to humans.     

Investigating interactions of phenanthrene with dissolved organic matter: limitations of Stern-Volmer plot

Although linear binding isotherms of hydrophobic organic chemicals (HOCs) with dissolved organic matter (DOM) are widely reported, several studies showed nonlinear HOC-DOM interactions. This study pointed out that fluorescence static quenching modeling (FSQM), which often uses a Stern-Volmer type plot to process the data from fluorescence quenching experiments, is conceptually different from the classic Stern-Volmer equation. We also emphasized that although linear Stern-Volmer plots are generally observed in literature, it does not necessarily indicate a linear HOC-DOM interaction. According to both mathematical simulation and laboratory sorption experiments in this study, nonlinear interactions could be concealed by the use of Stern-Volmer plot. Moreover, this study tested the two assumptions for applying FSQM to process binding data. Our results showed that binding coefficient (K(DOC)) for phenanthrene is neither independent of free solute concentration, nor DOM concentration, which is a critical limitation for using FSQM in a form of Stern-Volmer equation to examine HOC-DOM interactions. Therefore, the true characteristics of HOC-DOM interactions need to be examined using different ways of experimental design and data processing.