环境因素对芦苇湿地CH4排放的影响

用封闭式箱法对辽河三角洲芦苇湿地温室气体CH₄ 排放进行了长期观测 .结果表明 ,CH₄ 排放有明显的季节变化规律 ,平均通量为 520μg·m^-2·h^-1.土壤产CH₄ 活性主要发生在0～5cm土层中 ,并随土层深度的增加而显著下降 .CH₄排放受环境因素影响很大 ,土壤氧化还原电位在 -110mV时就有CH₄排放 ,其排放量随氧化还原电位的下降而增加 .另外 ,随着淹水深度的增加 ,CH₄ 排放反而减少 .在测定期内 ,CH₄ 排放与温度呈明显的正相关 (R²=0196,n=21,P<0.05).     

土壤理化特性对稻田CH4排放的影响

为了研究土壤理化特性对稻田CH4 排放的影响 ,室外盆栽试验于 2 0 0 0年水稻生长季在南京农业大学实施 ,1 8个供试水稻土分别取自江苏宜兴、江宁、六合、仪征及宝应等地 .所有供试土壤的季节性CH4 平均排放通量为 6 42± 2 70mg·(m2 ·h) - 1,最低和最高值分别为 1 96mg·(m2 ·h) - 1和 1 1 0 6mg·(m2 ·h) - 1,两者相差约 5 6倍 .单相关分析结果表明 :影响CH4 排放的主要土壤参数为质地、氮素状况及铜含量 .CH4 排放与土壤砂粒含量呈正相关 (r =0 5 2 8,p =0 0 2 4) ,与粘粒含量呈负相关 (r =-0 484,p =0 0 42 ) .氮素含量高的土壤CH4 排放较低 ,CH4 排放与土壤全氮、速效氮和铵态氮含量的线性相关系数分别为 -0 449(p =0 0 62 )、-0 61 1 (p =0 0 0 7)和 -0 649(p =0 0 0 4) .土壤铜含量直接影响CH4 的排放 ,CH4 排放与有效态铜和全铜含量的线性相关系数分别为 -0 5 94(p =0 0 0 9)和 -0 5 47(p =0 0 1 9) .本研究并未观测到CH4 排放与土壤有机碳含量有相关关系 ,这与前人报道的实验室培养测定结果及稻田CH4 排放随土壤有机质含量提高而增加的假设完全不同 .逐步回归分析表明 ,不同土壤间CH4 排放的变异性有 75 5 %可由土壤有效态铜含量、镁 (全量 )含量及有效铁含量与全量铁之     

环境气象学、环境空气动力学

X 16 X1449700086淹水土壤中甲烷产生的影响因素研究进展/颜晓元…(中科院南京土壤研究所)//环境科学进展/中科院生态环境研究中心一1996,4(2)一24~32环信X一4 综述了几种因索对土壤产生CH;的影响及其作用机理:一、土壤氧化还原电位,实验表明,氧化还原电位越低,CH4生成量越大,当Eh从一200降到一300mV时,CH。生成量增加10倍,排放量增加17倍。认为Eh:①直接影响CH;的产生量和产生速率,②使水稻植株发生形态上和生理上的改变而影响CH;的产生和排放。二、有机质,土壤中可溶性有机碳的含里随所加有机质量的增加而增加,而水溶性碳的含星与C…     

厌气条件下百菌清对土壤N2O和CH4排放的影响

在密闭、淹水、充N2的严格厌氧条件下对土壤进行了14d的培养试验,研究了杀菌剂百菌清在添加水平为田间施用量（FR）(5.5 mg·kg-1),20倍(20FR)和40倍田间施用量(40FR)时对强酸性、酸性、中性和碱性土壤N2O和CH4排放的影响.结果表明,20FR和40 FR的百菌清能够显著促进N2O向N2的还原,降低N2O排放,在酸性、中性和碱性土壤中培养14d后,对照处理的N2O排放量为0.076~0.46mg·kg-1,而20FR和40FR处理的N2O排放量为0.004~0.06mg·kg-1,降低了１个数量级.反硝化作用和有机氮矿化作用强的土壤中,百菌清减少N2O排放作用更明显.反硝化底物NO-3的存在对CH4的产生与排放具有显著的抑制作用.在加入百菌清未对NO-3浓度产生显著影响的土壤中,百菌清对CH4排放量没有明显影响,在对NO-3浓度产生显著影响的土壤中,CH4排放量随着NO-3的增加而减少,说明百菌清可能通过影响反硝化过程中NO-3的消耗而影响CH4排放.     

若尔盖高原沼泽土壤氧化甲烷的研究

若尔盖高原泥炭沼泽土氧化大气 CH₄ 的速率为 0.97～1.69ng/(g·h),氧化速率随着土壤深度的增加而减小;而泥炭土 CH₄ 排放速率为0.37～0.61ng/(g·h).2种土壤均具有氧化8000μL/L高浓度CH4的能力,泥炭沼泽土的潜力比泥炭土的大.不同土壤层次氧化甲烷的潜力也有差异,表层土比下层土高.降水减少导致的沼泽水位下降将加强若尔盖高原沼泽土壤氧化 CH₄ 从而减少沼泽 CH₄ 排放.     

不同施氮处理下旱作农田土壤CH_4、N_2O气体排放特征研究

依托甘肃农业大学布设在定西市李家堡镇的长期施氮定位实验,对不同施氮农田CH4和N2O气体通量,采用静态箱-气相色谱法进行小麦生育期的连续观测,并对影响通量变化的环境因子同期观测.结果表明:5个施氮处理下(0、52.5、105、157.5、210 kg·hm-2),旱作农田土壤在小麦全生育期内表现为CH4累积通量的汇和N2O累积通量的源;且不施氮处理时,CH4累积吸收通量最大;施氮量为210 kg·hm-2时,土壤CH4的累积吸收通量所受抑制最大,即土壤CH4累积吸收通量随施氮量升高而降低.相反,不施氮处理时,土壤N2O的累积排放通量最小,施氮量为210 kg·hm-2时,土壤N2O的累积排放通量最大,土壤N2O累积排放通量随施氮量的增加而增大.综合分析,施氮量增大会抑制全生育期旱作春小麦田土壤CH4吸收通量,提高土壤N2O的排放通量.因此,合理控制施氮量有利于生育期旱作农田土壤减排.CH4平均吸收通量随土壤温度的升高而降低,随土壤水分的升高而升高;相反,N2O平均排放通量随土壤温度的升高而升高,随土壤水分的升高而降低.5~10 cm层次的土壤温度与CH4平均吸收通量呈极显著线性负相关,与N2O平均排放通量呈显著正相关.5~10 cm层次的土壤水分与CH4平均吸收通量呈极显著线性正相关,与N2O平均排放通量呈显著负相关.     

脱硫石膏对稻田CH4释放及其功能微生物种群的影响

为探究脱硫石膏对温室气体CH_4排放及其功能微生物种群的影响,采用静态暗箱/气相色谱法,高通量测序和荧光定量PCR技术,研究了FGDG0(0 t·hm~(-2))、FGDG1(2 t·hm~(-2))、FGDG2(4 t·hm~(-2))、FGDG3(8 t·hm~(-2))、FGDG4(16 t·hm~(-2))这5个施加脱硫石膏处理下CH_4排放特征、稻田细菌群落结构及产甲烷菌和甲烷氧化菌丰度的变化.结果表明施加脱硫石膏后,土壤p H显著提高(P0.05),土壤氧化还原电位、有机质、速效钾含量增加,但处理间无显著差异(P0.05);稻田CH_4平均排放通量随着脱硫石膏用量增加而降低,且FGDG1FGDG2FGDG3FGDG4,较对照分别减少31.56%、57.30%、83.60%、90.66%;与对照相比,FGDG1、FGDG2处理增加了土壤细菌丰富度和多样性,但用量超过4 t·hm~(-2)后,细菌丰富度和多样性逐渐降低;与对照相比,稻田土壤硫酸盐还原菌属相对丰度显著提高6.98%~13.56%,甲烷氧化菌pmo A基因丰度增加0.3%~6.2%,产甲烷菌mrc A基因丰度显著下降2.4%~15.8%,且丰度比(pmo A/mcr A)随着脱硫石膏用量增加而增大;相关性分析表明,CH_4平均排放通量与土壤中硫酸盐还原菌属相对丰度呈显著负相关,与产甲烷菌mcr A基因丰度呈显著正相关,与pmo A/mcr A比呈显著负相关.综上,脱硫石膏能够提高稻田土壤细菌群落多样性,抑制稻田CH_4排放.     

南极法尔兹半岛植被土壤CH_4通量特征

应用密闭箱法首次测定了南极法尔兹半岛苔藓、地衣植被土壤CH4 排放通量 ,并估算了该半岛植被土壤在夏季 2个月内CH4 的排放总量 .结果表明 :在晴好天气条件下 ,苔藓土壤CH4 排放通量可能呈现双峰型变化特征 ;而在雨、雪等复杂多变的天气条件下 ,CH4 通量变化无规则 ,存在较大的时空变化 ,且与温度的响应关系不明显 ;苔藓土壤CH4 通量夏季变化的主要影响因子是温度 ,同时还受降水的影响 .苔藓土壤吸收CH4 总量为 0 6 6 5 3× 10 2 kg ;地衣土壤吸收CH4 总量为 0 76 0 3×10 2 kg .由此可见 ,该半岛苔藓、地衣植被土壤起着大气CH4 汇的作用     

生物炭添加对半干旱地区土壤温室气体排放的影响

为确定生物炭添加对半干旱地区农田土壤温室气体释放的影响,采用小区定位试验,利用锯末(J)和槐树皮(H)及3种添加比例(1%、3%、5%,质量百分比),研究了生物炭添加6个月内表层土壤CO2、CH4和N2O等3种温室气体排放的动态变化.结果表明,与对照相比,各处理土壤CO2排放通量随生物炭的添加呈现增加的趋势,锯末和槐树皮等两种生物炭处理的土壤CO2平均排放通量分别增加了1.89%和3.34%,但差异不显著.CH4排放随着生物炭添加量的增加而降低,各生物炭处理的土壤表层CH4排放量平均降幅分别为:J1:1.17%、J3:2.55%、J5:4.32%、H1:2.35%、H3:5.83%、H5:7.32%.其中,锯末生物炭仅在5%添加量时较对照差异显著(P0.05),而槐树皮生物炭处理在3%和5%的添加量与对照差异均达显著水平(P0.05).生物炭对N2O的排放影响没有明显规律性.研究表明,生物炭在短期内对半干旱地区农田土壤CO2和N2O的排放没有显著影响,而对CH4排放则影响显著(P0.05).就生物炭类型而言,槐树皮生物炭在抑制CH4排放方面优于锯末生物炭,差异显著(P=0.048).     

小兴安岭毛赤杨沼泽CH4、N2O排放规律及其对人为干扰的响应

选择小兴安岭山区毛赤杨（Alnus sibirica）沼泽为研究对象,利用静态暗箱-气相色谱法,研究两个生长季内（2007年和2008年）沼泽湿地在自然状态下CH4、N2O排放通量的变化规律及其主要影响因素,以及在不同采伐干扰（皆伐、45%择伐）方式下,CH4和N2O排放通量的变化过程.结果表明,2007年CH4和N2O平均排放通量分别为1.03 mg·m-2·h-1和58.56μg·m-2·h-1,2008年分别为20.57 mg·m-2·h-1和17.41 μg·m-2·h-1; CH4排放高峰期均发生在夏、秋两季,N2O排放规律不明显.皆伐沼泽和45%择伐沼泽CH4平均排放量分别为597.06、237.05 μg·m-2·h-1,N2O平均排放量分别为35.84、114.51μg·m-2·h-1;与天然沼泽相比,CH4排放量明显下降,N2O排放通量明显升高.水位是CH4排放的主要影响因子,但当水位达到一定高度时不再成为限制因子,土壤温度与CH4排放相关性显著,相对较低水位与相对较高土壤温度有利于N2O排放;积水水位是影响沼泽不同年份CH4和N2O通量排放差异的主要影响因子,采伐引起的土壤温度和水位的变化是干扰地与对照地CH4和N2O排放产生差异的主要原因.     

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.     

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.     

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

ＲｅｍｏｖａｌｏｆｈｅａｖｙｍｅｔａｌｓｆｒｏｍｓｅｗａｇｅｓｌｕｄｇｅｂｙｌｏｗｃｏｓｔｉｎｇｃｈｅｍｉｃａｌｍｅｔｈｏｄａｎｄｒｅｃｙｃｌｉｎｇｉｎａｇｒｉｃｕｌｔｕｒｅＷｕＱｉｔａｎｇ，ＮｙｉｒａｎｄｅｇｅＰａｓｃａｓｉｅ，ＭｏＣｅｈｕｉＦ...