滇池氮与富营养化研究

通过利用滇池外海多年来的监测结果,从宏观上的污染物总量和微观上的数理统计分析提出,进入滇池湖体的氮磷总量中,氮对滇池的贡献要远大于磷;夏季主要以COD、BOD有机污染为主,冬季以氮、磷污染为主.因此,解决滇池富营养化的根本途径是点源、面源综合治理,彻底减少TN、TP、COD和BOD的排放量.     

草海底泥疏浚问题

占滇池面积2.7％的草海(8.15平方公里),所接纳的污水占滇池纳污总量的44.83％,污水中有41.2—56.9％的污染物沉积于草海内,使草海底质受到重金属、有机物质、尤其是氮和磷营养物质的严重污染。沉积于草海底泥中的氮、磷污染物在适当条件     

滇池流域高分辨率氮、磷排放清单

氮、磷富集是我国浅水湖泊水质恶化和水生态退化的关键原因之一,但以往流域尺度氮、磷排放清单不足以精确识别排放的空间异质性和满足地表过程数值模拟的分辨率要求.为了提高控源减排措施的针对性,以滇池流域为例建立其高分辨率氮、磷排放清单.通过现场调查、采样观测与资料收集,确定各污染源的活动水平和修正排放因子,基于GIS平台核算企业源(工业、第三产业)、生活源(城镇、农村)、城市源(暴雨径流)、农业源(种植业)等7种点源和非点污染源在110个子流域的氮、磷排放量(平均分辨率约5 km×5 km).主要结论包括:①2008年滇池流域氮、磷排放总量分别为10736 t和542 t,且以城镇生活点源为主,占72.7％和42.8％;②氮、磷排放空间异质性十分明显,子流域氮、磷排放总量分别为(97.6±291.7)t(1个标准方差)和(4.93±11.8)t,其中全流域70％的氮、磷排放量仅集中在占流域面积16.2％的10个子流域和37.9％的21个子流域,而排放量最大的是盘龙江上游(氮、磷分别占21.9％和20.2％);③各污染源的排放格局异质性也大,对于氮而言,除了滇池北岸城区和沿流域边界的外围子流域以城镇生活和种植业为最大污染源,东、南、西岸湖盆区大部分则以其他污染源为主;相比而言,磷排放的各子流域最大污染源差异性更大;④通过与传统分辨率结果的比较,高分辨率排放清单能够更为准确甄别排放格局异质性、污染类型等信息,更加有利于明确控源减排的措施、布局和规模.     

滇池沉积物间隙水中氮、磷形态及相关性的研究

对滇池40个样点沉积物间隙水中的氮、磷形态与浓度分析研究结果表明，滇池沉积物间隙水中磷的区域分布特征与其在水体中的分布特征相似，滇池南部间隙水中无机磷浓度较高，有机磷的浓度极低，而北部有机磷浓度较高；间隙水中氨氮（NH4^＋ -N），浓度高出硝酸盐氮（NO3^- -N）浓度约2个数量级，间隙水中氮向上覆水的扩散主要以氨氮为主．滇池沉积物间隙水中氮、磷浓度远高于水体中氮磷浓度，有较强的释放趋势．进一步研究间隙水中氮、磷的关系则表明，沉积物间隙水中总磷和总氮未见明显相关性，但间隙水中总磷、有机磷均与硝酸盐态氮呈负相关．     

滇池面源污染及其综合治理

滇池面源污染物主要是N、P、COD和BOD5，来源于水土流失、湖面直接进入、地表径流、农田不合理施肥以及农村生活废弃物及乡镇企业污染。应通过小流域治理、发展生态农业和修沿湖污工程进一步加以治理。     

滇池水质时间序列变化趋势识别及特征分析

应用STL(Seasonal-Trend Decomposition using LOESS)方法对1998—2010年滇池外海8个监测站点、10个水质指标的时间序列数据进行递归迭代,分解出低频率的趋势项、高频率的周期项及随机残差项.在此基础上计算稳态变化指数(RSI),对水质趋势的时、空变化特征进行识别和判定.结果表明,在分析的13年间,滇池外海8个监测站点各指标变化趋势总体一致;BOD5总体呈下降趋势,高锰酸盐指数(COD Mn)总体趋势显著上升,说明有机物可生化性下降;富营养化状态加剧,总氮(TN)总体趋势上升,并逐渐成为藻类的限制性营养盐,总磷(TP)浓度为劣V类,氨氮在氮元素形态中的主导地位正逐渐降低.研究结果表明,"十二五"期间滇池应重点控制氮磷、兼顾有机物污染.     

水质污染的研究概况

水质污染的防治是关系到国计民生的重要问题.本文概述了我国水质污染防治的情况;介绍了COD、BOD、氰化物、砷、重金属、物理性状、富营养化等检测项目的监测方法及遥感技术在水质污染监测上的应用情况;根据不同行业和不同的污染物,列举了有关的水处理方法,并涉及除磷、除氮、絮凝剂的应用,含油污水的处理及其它水处理措施.     

化学法一步深度处理城市污水的研究

采用化学法一步深度处理城市污水（COSDT），可在降低COD、BOD的同时，除磷、去氮、灭菌。经该方法处理后的城市污水可用于农田灌溉、绿化用水。     

滇池流域农田氮、磷肥施用现状与评价

2001年6月至9月分别对流域内晋宁，呈贡，西山，官渡和嵩明调查了365家农户有关化肥施用情况，调查分析和计算表明，每年从种植业流失的化肥中纯氮（N）达2575t，纯磷（P）达218t，蔬菜和花卉地的单位面积氮流失量是水田和旱地的7-20倍。菜地年每公顷流失氮204kg，水田的氮流失量最低，平均每公顷每年流失10kg。磷的流失也以蔬菜，花卉地为最高，蔬菜和花卉地的单位面积磷流失量是水田和旱地的9-10倍。研究结果证明，大量的氮，磷化肥施用，通过地表径流和地下水流入滇池是造成其水体富营养化的重要原因之一^[6]，随着农业和农村经济的发展，蔬菜，花卉等经济作物在滇池流域的种植面积将会逐年扩大，因氮，磷化肥的施用面造成的氮，磷流失量将会不断加大，为了实现减少氮，磷化肥对滇池的污染，应积极推广精确施肥，平衡施肥等科学施肥技术，提高化肥利用率，减少化肥流失。增施有机肥，降低化肥用量，同时提高农村居民的环境意识，加强环境管理，依法保护农村环境，控制农业面源污染。     

梁平县境内高滩河水质的空间分布及其对土地利用方式的响应

以梁平县境内高滩河流域为研究对象,综合应用GIS空间分析、Pearson相关分析和RDA冗余分析方法,研究在子流域尺度上COD、BOD5、氨氮和总磷4种水质要素对土地利用方式的生态响应。结果表明:高滩河流域土地利用类型对水质要素有着重要影响,林地能够改善河道水环境,旱地和城镇村和工矿用地是COD、BOD5和氨氮的主要污染来源,园地、交通运输用地以及水域对污染物的影响较弱,说明农业面源污染和农村居民生活污染是高滩河水质恶化的主要原因。     

Toxic effects of acetochlor, methamidophos and their combination on nifH gene in soil

Toxic effects of two agrochemicals on nifH gene in agricultural black soil were investigated using denaturing gradient gel electrophoresis （DGGE） and sequencing approaches in a microcosm experiment. Changes of soil nifH gene diversity and composition were examined following the application of acetochlor, methamidophos and their combination. Acetochlor reduced the nifH gene diversity （both in gene richness and diversity index values） and caused changes in the nifH gene composition. The effects of acetochlor on nifH gene were strengthened as the concentration of acetochlor increased. Cluster analysis of DGGE banding patterns showed that nifH gene composition which had been affected by low concentration of acetochlor （50 mg/kg） recovered firstly. Methamidophos reduced nifH gene richness that except at 4 weeks. The medium concentration of methamidophos （150 mg/kg） caused the most apparent changes in nifH gene diversity at the first week while the high concentration of methamidophos （250 mg/kg） produced prominent effects on nifH gene diversity in the following weeks. Cluster analysis showed that minimal changes of nifH gene composition were found at 1 week and maximal changes at 4 weeks. Toxic effects of acetochlor and methamidophos combination on nifH gene were also apparent. Different nifH genes （bands） responded differently to the impact of agrochemicals： four individual bands were eliminated by the application of the agrochemicals, five bands became predominant by the stimulation of the agrochemicals, and four bands showed strong resistance to the influence of the agrochemicals. Fifteen prominent bands were partially sequenced, yielding 15 different nifH sequences, which were used for phylogenetic reconstructions. All sequences were affiliated with the alpha- and beta-proteobacteria, showing higher similarity to eight different diazotrophic genera.     

Arsenic uptake by arbuscular mycorrhizal maize （Zea mays L.） grown in an arsenic-contaminated soil with added phosphorus

The effects of arbuscular mycorrhizal (AM) fungus (Glomus mosseae) and phosphorus (P) addition (100 mg/kg soil) on arsenic (As) uptake by maize plants (Zea mays L.) from an As-contaminated soil were examined in a glasshouse experiment.Non-mycorrhizal and zero-P addition controls were included.Plant biomass and concentrations and uptake of As,P,and other nutrients,AM colonization,root lengths,and hyphal length densities were determined.The results indicated that addition of P significantly inhibited root colonization and development of extraradical mycelium.Root length and dry weight both increased markedly with mycorrhizal colonization under the zero-P treatments,but shoot and root biomass of AM plants was depressed by P application.AM fungal inoculation decreased shoot As concentrations when no P was added,and shoot and root As concentrations of AM plants increased 2.6 and 1.4 times with P addition,respectively.Shoot and root uptake of P,Mn,Cu,and Zn increased,but shoot Fe uptake decreased by 44.6%,with inoculation, when P was added.P addition reduced shoot P,Fe,Mn,Cu,and Zn uptake of AM plants,but increased root Fe and Mn uptake of the nonmycorrhizal ones.AM colonization therefore appeared to enhance plant tolerance to As in low P soil,and have some potential for the phytostabilization of As-contaminated soil,however,P application may introduce additional environmental risk by increasing soil As mobility.     

Degradation of metabolites accumulated of benzo[a]pyrene by coupling Penicillium Chrysogenum with KMnO4

Several main metabolites of benzo[a]pyrene （BaP） formed by Penicillium chrysogenum, Benzo[a]pyrene-1,6-quinone （BP 1,6- quinone）, trans-7,8-dihydroxy-7,8-dihydrobenzo[a]pyrene （BP 7,8-diol）, 3-hydroxybenzo[a]pyrene （3-OHBP）, were identified by high-performance liquid chromatography （HPLC）. The three metabolites were liable to be accumulated and were hardly further metabolized because of their toxicity to microorganisms. However, their further degradation was essential for the complete degradation of BaP. To enhance their degradation, two methods, degradation by coupling Penicillium chrysogenum with KMnO4 and degradation only by Penicillium chrysogenum, were compared; Meanwhile, the parameters of degradation in the superior method were optimized. The results showed that （1） the method of coupling Penicillium chrysogenum with KMnO4 was better and was the first method to be used in the degradation of BaP and its metabolites; （2） the metabolite, BP 1,6-quinone was the most liable to be accumulated in pure cultures; （3） the effect of degradation was the best when the concentration of KMnO4 in the cultures was 0.01% （w/v）, concentration of the three compounds was 5 mg/L and pH was 6.2. Based on the experimental results, a novel concept with regard to the bioremediation of BaP-contaminated environment was discussed, considering the influence on environmental toxicity of the accumulated metabolites.     

Impact of atrazine and nitrogen fertilizers on the sorption of chlorotoluron in soil and model sorbents

Sorption of chlorotoluron in ammonium sulfate, urea and atrazine multi-solutes system was investigated by batch experiments. The results showed application of nitrogen fertilizers to the soil could affect the behavior of chlorotoluron. At the same concentration of N, sorption of chlorotoluron decreased as the concentration of atrazine increased on the day 0 and 6 in soil, respectively. The sorption of chlorotoluron increased from 0 to 6 d when soils were preincubated with deionized water, ammonium sulfate and urea solution for 6 d. That indicated incubation time was one of the most important factors for the sorption of chlorotoluron in nitrogen fertilizers treatments. The individual sorption isotherms of chlorotoluron in rubbery polymer and silica were strictly linear in single solute system, but there were competition sorption between pesticides or between pesticides and nitrogen fertilizers. That indicated the sorption taken place by concurrent solid-phase dissolution mechanism and sorption on the interface of water-organic matter or water-mineral matter.     

Distribution and ecological effect of mercury in Laogang landfill, Shanghai, China

Laogang landfill near Shanghai is the largest landfill in China, and receives about 10000 t of daily garbage per day, Samples of topsoil and plants were analyzed to evaluate mercury pollution from the landfill. For topsoil samples, there were significant correlations among total mercury （HgT）, combinative mercury （Hgc） and gaseous mercury （HgG）, and content of total organic carbon （TOC）, but, no significantly relationship was found between Hg content and filling time. Hg content changes in vertical profiles with time showed that the average Hgv of profiles 1992, 1996, and 2000 was similar, but their average HgG was quite different. HgT was significantly correlated with Hgc in profile 1992 and 2000, and Hgv was significantly correlated with Hg6 in profile 1996. HgG/Hgv ratio in profile samples decreased in the order of （HgG,/HgT）1992〉（HgG/HgT）1996〉〉（HgG/HgT）2000. A simple outline of Hg release in landfill could be drawn： with increasing of filling time, degradation undergoes different biodegradation, accordingly, gaseous mercury goes through small, more, and small proportion to total mercury. Distribution of Hg in plants was inhomogeneous, following the order of leaf〉root〉stem. The highest value of leaf may be associated with higher atmospheric Hg from landfill. Ligneous plants （e.g. Phyllostachys glanca, Prunus salicina and Ligustrum lucidum） are capable of enriching more Hg than herbaceous plants.     

EDTA-enhanced phytoremediation of lead contaminated soil by Bidens maximowicziana

Phytoremediation is a potential cleanup technology for the removal of heavy metals from contaminated soils.Bidens maximowicziana is a new Pb hyperaccumulator,which not only has remarkable tolerance to Pb but also extraordinary accumulation capacity for Pb.The maximum Pb concentration was 1509.3 mg/kg in roots and 2164.7 mg/kg in overground tissues.The Pb distribution order in the B. maximowicziana was:leaf>stem>root.The effect of amendments on phytoremediation was also studied.The mobility of soil Pb and the Pb concentrations in plants were both increased by EDTA application.Compared with CK(control check),EDTA application promoted translocation of Pb to overground parts of the plant.The Pb concentrations in overground parts of plants was increased from 24.23-680.56 mg/kg to 29.07-1905.57 mg/kg.This research demonstrated that B.maximowicziana appeared to be suitable for phytoremediation of Pb contaminated soil,especially,combination with EDTA.     

Potential of plant polyphenol oxidases in the decolorization and removal of textile and non-textile dyes

In this study an effort has been made to use plant polyphenol oxidases; potato （Solanum tuberosum） and brinjal （Solanum melongena）, for the treatment of various important dyes used in textile and other industries. The ammonium sulphate fractionated enzyme preparations were used to treat a number of dyes under various experimental conditions. Majority of the treated dyes were maximally decolorized at pH 3.0. Some of the dyes were quickly decolorized whereas others were marginally decolorized. The initial first hour was sufficient for the maximum decolorization of dyes. The rate of decolorization was quite slow on long treatment of dyes. Enhancement in the dye decolorization was noticed on increasing the concentration of enzymes. The complex mixtures of dyes were treated with both preparations of polyphenol oxidases in the buffers of varying pH values. Potato polyphenol oxidase was significantly more effective in decolorizing the dyes to higher extent as compared to the enzyme obtained from brinjal polyphenol oxidase. Decolorization of dyes and their mixtures, followed by the formation of an insoluble precipitate, which could be easily removed simply by centrifugation.     

Decomposition of alachlor by ozonation and its mechanism

Decomposition and corresponding mechanism of alachlor, an endocrine disruptor in water by ozonation were investigated. Results showed that alachlor could not be completely mineralized by ozone alone. Many intermediates and final products were formed during the process, including aromatic compounds, aliphatic carboxylic acids, and inorganic ions. In evoluting these products, some of them with weak polarity were qualitatively identified by GC-MS. The information of inorganic ions suggested that the dechlorination was the first and the fastest step in the ozonation of alachlor.     

Enzymatic oxidation of aqueous pentachlorophenol

The influence of the nonionic surfactant Tween 80 on pentachlorophenol （PCP） oxidation catalyzed by horseradish peroxidase was studied. The surfactant was tested at concentrations below and above its critical micelle concentration （CMC）. Enhancement of PCP removal was observed at sub-CMCs. The presence of Tween 80 in the reaction mixture reduced enzyme inactivation which occurred through a combination of free radical attack and sorption by precipitated products. A simple first-order model was able to simulate time profiles for enzyme inactivation in the presence or absence of Tween 80. At supra-CMCs, the surfactant caused noticeable reductions in PCP removal, presumably through micelle partitioning of PCP which precluded the hydrophobic PCP molecule from interacting with the enzyme.     

Removal of heavy metals from sewage sludge by low costing chemical method and recycling in agriculture

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