自然土壤中苯酚降解菌的分离和系统发育分析

采用富集培养的方法,从未受苯酚污染的自然土壤中分离得到5株能以苯酚为唯一碳源生长的细菌.根据生理生化特性和系统发育分析对它们进行了初步鉴定,菌株PHD-2为Ralstonia sp.,菌株 PHD-4为Acinetobacter sp.,菌株PHD-5 为Microbacterium sp.,菌株PHD-1和PHD-3均为Pseudomonas sp.,16S rRNA基因序列的同源性比较和系统发育分析表明自然土壤中的苯酚降解菌具有丰富的多样性.     

强化供氧条件下潜流型人工湿地运行特性

针对潜流型人工湿地中溶解氧浓度和脱氮率偏低的问题,试验研究了强化供氧对植物和微生物的影响及人工湿地内溶解氧浓度、净化效率的变化规律.结果表明,强化供氧宜在湿地前端进行,最佳气水比为6左右,可采用连续供氧方式.供氧对湿地植物生理特性无明显不良影响,可显著增加湿地中硝化菌、反硝化菌数量,硝化菌可比供氧前高出1～2个数量级,反硝化菌高出1个数量级.强化供氧有效改善了湿地内氧环境,供氧前湿地内溶氧浓度普遍低于0.6 mg/L,供氧后氧浓度上升至1 mg/L以上.强化供氧有利于各类污染物质尤其是有机物和氮类物质的去除,有机物去除率比原湿地高出10％左右, TN去除率能够达到60％以上.因此,强化充氧措施具有较好的研究和应用价值.     

某天然气净化厂污水处理装置改造可行性研究

通过多次的现场调研、收集资料和水质监测,分析了引进天然气净化厂生产的产污环节,现有的污水处理装置的有关设计图纸及污水处理的运行情况.在此基础上,采用理论分析与实际问题相结合的方式,针对现有污水处理过程中的不足,提出了该厂的污水处置适应性改造的可行性研究.     

臭氧对有机物混凝的影响

采用PDA(Photometric Disperse Analysis)和有机物表观分子量分级、有机物化学极性分级技术从絮体形成过程、絮体表现、有机物分子水平变化等方面研究了臭氧预氧化对混凝过程的影响;并对比了不同混凝剂在预臭氧条件下的混凝过程和效率.结果表明:臭氧预氧化对混凝过程有复杂的影响,其剂量和水体有机物特征决定了其对混凝的整体影响效果.有机物分级显示,臭氧化对有机物结构有重要影响,导致有机物极性、亲水性组分含量大幅提高(36.7%),小分子量组分(<10×10³)大幅增高(100%左右);但总的DOC去除率不高(3.28%).对PACl而言,在中、低剂量(O₃/TOC<0.7)下,臭氧对絮体形成过程影响较小,但对絮体沉降性和浊度去除已经有阻碍作用.在中、高剂量下(O₃/TOC>0.7),对絮体形成有显著滞后,浊度、有机物去除效率下降.AlCl₃对臭氧化作用反应敏感,臭氧化在试验剂量条件下,对絮体形成和浊度、有机物去除都有明显的阻碍作用.     

持久性有机污染物(POPs)生物修复研究进展

持久性有机污染物(POPs)具有高毒性和低可降解性的特征,通过先进的生物修复技术来治理POPs污染正受到公众普遍的关注.而提高生物可利用性则可以突破原位生物修复的瓶颈;宏基因组技术可以获得大量的降解基因资源;利用生物工程手段,可以大幅度提高降解菌的能力这3个方面是目前POPs生物修复领域的研究热点.     

污泥生物处理的研究与应用

污泥生物处理技术包括污泥前置及后置的处理。污泥前置处理可以通过微生物自身的新陈代谢和微生物种群之间捕食作用,以及对工艺和反应器的改良来实现污泥减量。污泥后置生物处理是指污泥消化,可以使用高温-中温共相厌氧消化和蛋形污泥消化器对污泥进行减量;这些方法从不同侧面反应了目前污泥生物处理研究现状以及最新进展。     

磷对云龙湖富营养化优势藻及混合藻生长的影响

氮磷等营养盐的增加和藻类的过度增殖是富营养化的主要标志。大多数湖泊水体富营养化受磷元素的制约。研究表明富营养化水体的不同藻类对磷含量的依赖性各不相同。通过研究在相同氮浓度,相同温度条件下,不同磷浓度对纯种小球藻和硅藻以及天然混合藻生长速度的影响,发现在氮浓度充足的情况下,磷含量高促进小球藻生长;对硅藻却没有明显的相关性;天然水体混合藻生长速度与磷浓度呈正相关。     

Ecological effects of crude oil residues on the functional diversity of soil microorganisms in three weed rhizospheres

Ecological effects of crude oil residues on weed rhizospheres are still vague. The quantitative and diversity changes and metabolic responses of soil-bacterial communities in common dandelion （Taraxacum officinale）, jerusalem artichoke （Silphiurn perfoliatum L.） and evening primrose （A colypha australis L.） rhizospheric soils were thus examined using the method of carbon source utilization. The results indicated that there were various toxic effects of crude oil residues on the growth and reproduction of soil bacteria, but the weed rhizospheres could mitigate the toxic effects. Total heterotrophic counting colony-forming units （CFUs） in the rhizospheric soils were significantly higher than those in the non-rhizospheric soils. The culturable soil-bacterial CFUs in the jerusalem artichoke （S. perfoliatum） rhizosphere polluted with 0.50 kg/pot of crude oil residues were almost twice as much as those with 0.25 kg/pot and without the addition of crude oil residues. The addition of crude oil residues increased the difference in substrate evenness, substrate richness, and substrate diversity between non-rhizospheric and rhizospheric soils of T. officinale and A. australis, but there was no significant （p〉0.05） difference in the Shannon＇s diversity index between non-rhizospheric and rhizospheric soils of S. perfoliatum. The rhizospheric response of weed species to crude oil residues suggested that S. perfoliatum may be a potential weed species for the effective plant-microorganism bioremediation of contaminated soils by crude oil residues.     

Investigation on Fe, Mn, Zn, Cu, Pb and Cd fractions in the natural surface coating samples and surficial sediments in the Songhua River, China

Natural surface coating samples （NSCSs） from the surface of shingles and surficial sediments （SSs） in the Songhua River, China were employed to investigate the relationship between NSCSs and SSs in fractions of heavy metals （Fe, Mn, Zn, Cu, Pb, and Cd） using the modified sequential extraction procedure （MSEP）. The results show that the differences between NSCSs and SSs in Fe fi＇actions were insignificant and Fe was dominantly present as residual phase （76.22% for NSCSs and 80.88% for SSs） and Fe-oxides phase （20.33% for NSCSs and 16.15% for SSs）. Significant variation of Mn distribution patterns between NSCSs and SSs was observed with Mn in NSCSs mainly present in Mn-oxides phase （48.27%） and that in SSs present as residual phase （45.44%）. Zn, Cu, Pb and Cd were found dominantly in residual fractions （〉48%）, and next in solid oxides/hydroxides for Zn, Pb and Cd and in easily oxidizable solids/compounds form for Cu, respectively. The heavy metal distribution patterns implied that Fe/Mn oxides both in NSCSs and SSs were more important sinks for binding and adsorption of Zn, Pb and Cd than organic matter （OM）, and inversely, higher affinity of Cu to OM than Fe/Mn oxides in NSCSs and SSs was obtained. Meanwhile, it was found that the distributions of heavy metals in NSCSs and SSs were similar to each other and the pseudo-total concentrations of Zn, Cu, Pb and Cd in NSCSs were greater than those in SSs, highlighting the more importance for NSCSs than SSs in controlling behaviours of heavy metals in aquatic environments.     

生态环境损害赔偿诉讼：定义与定位矫正

面对生态环境损害赔偿诉讼这一新型诉讼形式,准确把握其定义和定位至关重要。现有生态环境损害赔偿诉讼按国家自然资源所有权私权化路径进行制度构建,其现行定义为特殊私益诉讼,现行定位为环境行政替代工具。这种定义与定位导致其与环境公益诉讼割裂,运行序位上优先于环境民事公益诉讼,引起国家机关角色错位。生态环境损害赔偿诉讼与环境民事公益诉讼的诉讼标的相同,救济和保护的利益均为环境公益,其定义应回归公益诉讼本位;政府在环境公益保护上有着广泛的职权和手段,是环境公共治理的优先主体,仅在少数行政不能的情形下才有借助司法的必要性和合理性,其在定位上应作为环境行政执法的补充机制在有限范围内发挥作用。据此,生态环境损害赔偿诉讼在制度体系上应与既有环境民事公益诉讼置于同一诉讼系属统筹立法,在诉讼序位上应让位于社会组织提起的环境民事公益诉讼。