城市浅水湖泊雨水溢流总磷输运的数值模拟

从三维对流-扩散-反应方程出发,根据雨水箱涵溢流入湖总磷形态特性,推导雨水溢流进入城市浅水湖泊后二维总磷的输运方程,并与浅水流动方程结合,建立城市浅水湖泊平面二维水流-水质总磷的数学模型.模型通过深圳荔枝湖实测资料验证,计算结果较好.用此模型计算设计降雨强度28 mm/h历时1 h情况下,雨水径流通过箱涵溢流进入荔枝湖和湖水混合后总磷输运情况,分析了入湖雨水总磷归趋.结果表明,溢流入湖TP通量为15.385 kg,其中62.3%掺混在水体中,28.1%沉积到表层底泥;污染后的湖水通过水污染治理工程连续运行3.0 d可将荔枝湖TP恢复到雨前初始浓度水平.     

城市浅水型湖泊底泥磷释放特性实验研究

通过对城市浅水型湖泊 (以南京玄武湖为例 )底泥磷释放特性进行实验研究 ,分析了环境因子对底泥磷释放特性的影响及其原因。得出了溶解氧、pH值、温度和扰动对底泥磷释放的影响曲线。同时说明了湖泊内源性磷对湖泊水质存在着潜在的危险性 ,为城市浅水型湖泊底泥疏浚和富营养化治理提供依据。     

热带浅水城市湖泊富营养化水体修复中生物操纵的研究

从生物操纵的来由、生物操纵的研究开展到生物操纵的局限,较为全面的体现了生物操纵在湖泊富营养化水体修复中所起的作用,并提出生物操纵的研究展望,提供了生物操纵在典型热带浅水城市湖泊-惠州西湖的实践案例研究,期为生物操纵在热带浅水城市湖泊深入研究提供一定的参考。     

城市浅水型湖泊底泥磷释放的环境因子影响实验研究

通过对城市浅水型湖泊（以南京玄武湖为例）底泥磷释放特性进行实验研究，分析了环境因子对底泥磷释放特性的影响及其原因。得出了溶解氧、pH值、温度和扰动对底泥磷释放的影响曲线。同时说明了湖泊底泥磷对湖泊水质存在着潜在的危险性。为城市浅水湖泊底泥疏浚和营营养化治理提供依据。     

风浪对湖泊沉积物再悬浮的影响及工程抑制研究

风浪引起沉积物再悬浮会直接影响水体光照条件,促进沉积物中污染物的释放,对湖泊生态系统的构建产生着重要影响。采用已发表数据验证了风浪要素和风浪切应力经验计算公式在浅水湖泊中的适应性,并从浅水湖泊风浪扰动机理出发,提出了临界起动应力简化计算方法和适用条件并加以验证。最后,基于简化模型和风致再悬浮影响评估方法研究了风浪对金湖水生态修复的影响,结合生态围隔、综合底质改良剂和复合微生物菌剂等综合措施,恢复金湖沉水植物150万m²。研究结果可用于评估风浪对浅水湖泊沉积物再悬浮的影响,为浅水湖泊水生态修复、内源污染治理工程设计提供理论参考。     

我国东部浅水湖泊水生态效应特征

为探究我国东部浅水湖泊生态系统的时空异质性及其演替的响应指标,基于东部浅水湖泊长时间序列（1986-2014年）的监测数据,分析了不同湖泊类型的水质和浮游植物群落分布特征,并综合运用稳态转换理论和典范对应分析方法（CCA）,研究了富营养化湖泊浮游植物群落的演替特征以及响应因子.结果表明:①从水系上看,太湖水系湖泊的水质最差,ρ（TP）、ρ（TN）和ρ（Chla）最高,分别为（0.276±0.606）（3.563±1.430）mg/L和（14.801±10.117）μg/L,SD（透明度）为（0.486±0.272）m;从水文连通性上看,湖泊的水质为通江湖泊>非通江湖泊>阻隔湖泊.②空间分布上,湖口以下干流浮游植物密度最高,为2.674×107 L-1.蓝藻门为东部浅水湖泊的优势种群,密度最高达1.897×107 L-1,绿藻门和硅藻门次之,黄藻门最少,仅为3.951×103 L-1.③东部浅水湖泊生态系统演替发生在ρ（Chla）为5.21~10.57 μg/L阈值范围内.④以东部典型湖泊-太湖为例,浮游植物群落分别在1997-1998年和2000-2001年两个时间梯度达到最大值.EC（电导率）和ρ（TN）是影响太湖浮游植物群落分布的显著因子.研究显示,随着东部浅水湖泊水质恶化,浮游植物群落结构特征发生突变,导致其生态系统发生演替,预防东部浅水湖泊生态系统演变应严控EC和ρ（TN）.      

长江中下游浅水湖泊沉积物中磷的形态及其与水相磷的关系

研究了长江中下游22个不同生态类型的浅水湖泊表层沉积物中磷的地球化学形态及水相磷含量等水质特征.对沉积物中磷形态的连续提取分析发现,自然粒度下,绝大部分湖泊的沉积物中90%以上的磷是以生物较难利用的形态存在的,活性磷所占比例很小.而在严重污染的城市湖泊中,活性磷含量则可以占到总磷的35%以上.沉积物中活性磷含量的高低与总磷含量并不一致.水草的存在对水相磷含量及沉积物中磷的活性都有显著的影响.水相磷的含量与沉积物中交换态磷的含量、沉积物铁磷比有显著的相关关系.研究表明,沉积物地球化学性质、水体营养盐含量及浅水湖泊生态类型之间存在复杂而密切的联系.     

“绿色流域建设”的湖泊富营养化防治思路及其在洱海的应用

虽然经过“十一五”阶段的治理,但我国湖泊富营养化形势依然严峻,湖泊富营养化治理仍然是目前我国水环境领域最为艰巨的任务之一. 根据长期在湖泊富营养化治理领域的研究与实践经验,提出我国应“立足流域进行统筹规划和治理,建设湖泊绿色流域”的湖泊富营养化防治思路. 通过梳理和提炼,提出了湖泊绿色流域构建的六大体系,即“产业结构调整控污减排、污染源工程治理与控制、低污染水处理与净化、清水产流机制修复、湖泊水体生境改善、流域系统管理与生态文明建设”. 同时,将“湖泊绿色流域建设”思路应用在洱海水污染防治工作中,针对洱海水污染特征与治理定位,提出了洱海水污染防治的技术路线,构建了洱海绿色流域建设的六大体系.      

典型城郊湖泊沉积物重金属生态风险评价

城郊浅水湖泊沉积物通常受到不同程度的污染,并面临重金属污染积累和生态风险增加的问题。以典型城郊浅水湖泊北麻漾近岸表层沉积物为研究对象,分析各重金属的分布特征,并利用地积累指数法(Igeo)和潜在生态风险指数法(RI)评价重金属生态风险。结果表明:表层沉积物中Cr、Ni、Cu、Zn、Cd、Pb含量均不同程度超过环境背景值,体现出一定的污染积累特征;地积累指数法评价所得风险顺序为Cu>Cd>Zn>Ni>Pb>Cr>Hg,潜在生态风险指数法获得单一重金属潜在生态风险顺序为Cd>Hg>Cu>Pb>Ni>Cr>Zn,两种评价结果均显示出以Cd为主,多种重金属复合污染的特征。综合潜在生态风险指数表明入湖河口区风险等级较高,外源输入对沉积物重金属污染影响显著。     

杭州西湖“香灰土”沉积物轻、重有机质组成特征及其环境意义

为探索城市浅水湖泊高有机质含量沉积物中有机质污染特征及其与氮、磷等营养元素的关系,调查了西湖8个湖区沉积物柱状样不同深度泥层有机质含量及其轻、重组分和氮磷污染特征,通过与国内相关湖泊有机质组分的比较,定量刻画了西湖"香灰土"沉积物的有机质特征.结果表明,西湖沉积物属典型高有机质含量底质,不同湖区底泥有机质含量平均值为28~251 g·kg-1;不同湖区沉积物有机质含量差别很大,引水入口湖区比其他湖区的有机质含量明显偏低;垂向上,大多湖区有机质含量随深度增加而增加,反映出有机质在西湖丰富的沉积历史.有机质轻/重组分离研究表明,西湖沉积物中轻组有机质含量为0.57~9.17 g·kg-1,平均占总有机质的2.83%,重组含量为5.35~347.41 g·kg-1,平均占总有机质的90%;与玄武湖、月湖、太湖、白洋淀等浅水湖泊相比,西湖底泥轻组有机质含量与之相当,但重组有机质含量明显偏高,反映出西湖作为历史悠久的城市湖泊,有机质污染负荷高,底泥腐殖化程度高.西湖底泥轻组有机质与总磷、总氮显著相关,而重组有机质含量仅与总氮含量显著相关,与磷没有相关性,表明轻组有机质对氮、磷内源释放潜力具有较大的影响.研究表明,西湖"香灰土"型沉积物有机质含量高、重组有机质比例高,对内源氮磷释放的缓冲能力强,在西湖营养盐内源负荷控制及水体富营养化治理中应予以充分考虑.     

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.     

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.     

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

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Single and joint effects of pesticides and mercury on soil urease

The influence of two pesticides including chlorimuron-ethyl and furadan and mercury （Hg） on urease activity in 4 soils （meadow burozem and phaeozem） was investigated. The soils were exposed to various concentrations of the two pesticides and Hg individually and simultaneously. Results showed that there was a close relationship between urease activity and organic matter content in soil. Chlorimuron-ethyl and furadan could both activate urease in the 4 soils. The maximum increment of urease activity by chlorimuronethyl was up to 14%-18%. There was almost an equal increase （up to 13%-21%） in the urease activity by furadan. On the contrary, Hg markedly inhibited soil urease activity. A logarithmic equation was used to describe the relationship （P〈0.05） between the concentration of Hg and the activity of soil urease in the 4 tested soils. Semi-effect dose （ED50） values by the stress of Hg based on the inhibition of soil urease in the 4 soils were 88, 5.5, 24 and 20 mg/kg, respectively, according to the calculation of the corresponding equations. The interactive effect of chlorimuron-ethyl or furadan with metal Hg on soil urease was mainly synergic at the highest tested concentrations.     

Isolation and preliminary characterization of a 3-chlorobenzoate degrading bacteria

A study was conducted to compare the diversity of 2-, 3-, and 4-chlorobenzoate degraders in two pristine soils and one contaminated sewage sludge. These samples contained strikingly different populations of mono-chlorobenzoate degraders. Although fewer cultures were isolated in the uncontaminated soils than contaminated one, the ability of microbial populations to mineralize chlorobenzoate was widespread. The 3- and 4-chlorobenzoate degraders were more diverse than the 2-chlorobenzoate degraders. One of the strains isolated from the sewage sludge was obtained. Based on its phenotype, chemotaxonomic properties and 16S rRNA gene, the organism S-7 was classified as Rhodococcus erythropolis. The strain can grow at temperature from 4 to 37℃. It can utilize several （halo）aromatic compounds. Moreover, strain S-7 can grow and use 3-chlorobenzoate as sole carbon source in a temperatures range of 10-30℃ with stoichiometric release of chloride ions. The psychrotolerant ability was significant for bioremediation in low temperature regions. Catechol and chlorocatechol 1,2-dioxygenase activities were present in cell free extracts of the strain, but no （chloro）catechol 2,3- dioxygenase activities was detected. Spectral conversion assays with extracts from R. erythropolis S-7 showed accumulation of a compound with a similar UV spectrum as chloro-cis,cis-muconate from 3-chlorobenzoate. On the basis of these results, we proposed that S-7 degraded 3-chlorobenzoate through the modified ortho-cleave pathway.     

Organochlorine pesticides in soils under different land usage in the Taihu Lake region, China

A field study was conducted in the Taihu Lake region, China in 2004 to reveal the organochlorine pesticide concentrations in soils after the ban of these substances in the year 1983. Thirteen organochlorine pesticides (OCPs) were analyzed in soils from paddy field, tree land and fallow land. Total organochlorine pesticide residues were higher in agricultural soils than in uncultivated fallow land soils. Among all the pesticides, ΣDDX (DDD, DDE and DDT) had the highest concentration for all the soil samples, ranging from 3.10 ng/g to 166.55 ng/g with a mean value of 57.04 ng/g and followed by ΣHCH, ranging from 0.73 ng/g to 60.97 ng/g with a mean value of 24.06 ng/g. Dieldrin, endrin, HCB and α-endosulfan were also found in soils with less than 15 ng/g. Ratios of p,p'-(DDD DDE)/DDT in soils under three land usages were: paddy field ＞ tree land ＞ fallow land, indicating that land usage inlfuenced the degradation of DDT in soils. Ratios of p,p'-(DDD DDE)/DDT ＞1, showing aged residues of DDTs in soils of the Taihu Lake region. The results were discussed with data from a former study that showed very low actual concentrations of HCH and DDT in soils in the Taihu Lake region, but according to the chemical half-lives and their concentrations in soils in 1980s, the concentration of DDT in soils seemed to be underestimated. In any case our data show that the ban on the use of HCH and DDT resulted in a tremendous reduction of these pesticide residues in soils, but there are still high amounts of pesticide residues in soils, which need more remediation processes.     

Sorption of 1-naphthol by plant cuticular fractions

The contribution of aliphatic-rich plant biopolymer to sorption of hydrophobic organic compounds is significantly important because of their preservation and accumulation in the soil environment,but sorption mechanism is still not fully understood.In this study, sorption of 1-naphthol by plant cuticular fractions was examined to better understand the contributions of respective fraction.Toward this end,cuticular materials were isolated from the fruits of tomato by chemical method.The tomato cuticle sheet consisted of waxes (6.5 wt%),cuticular monomer (69.5 wt%),and polysaccharide (24.0 wt%).Isotherms of l-naphthol to the cuticular fractions were nonlinear (N value (0.82-0.90)) at the whole tested concentration ranges.The KodKow ratios for bulk cuticle (TC1),dewaxed cuticle (TC2),cutin (TC4),and desugared cuticle (TC5) were larger than unity,suggested that tomato bulk cuticle and cutin are much powerful solption medium.Sorption capability of cutin (TC4) was 2.4 times higher than the nonsaponifiable fraction (TC3).The 1-naphthol interactions with tomato cuticular materials were governed by both hydrophobic-type interactions and polar (H-bonding) interactions. Removal of the wax and polysaccharide materials from the bulk tomato cuticle caused a significant increase in the sorption ability of the cuticular material.There was a linear negative trend between K_(oc) values and the amount of polysaccharides or fraction's polarities ((N O)/C);while a linear positive relationship between K_(oc) values and the content of cutin monomer (linear R~2=0.993) was observed for present in the cuticular fractions.Predominant sorbent of the hydrophobic organic compounds (HOCs) in the plant cuticular fraction was the cutin monomer,contributing to 91.7% of the total sorption of tomato bulk cuticle.