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1.
贵州省2002年酸雨污染情况分析   总被引:8,自引:1,他引:7  
为了准确及时地掌握贵州省的酸雨污染现状和发展趋势,为全省的酸雨控制提供科学依据,于2002 年3月至2003年2月在贵州省全省范围内进行年度降水pH值和离子组分监测。监测结果显示:全省降水pH年均值为5.38,个别城市降水pH年均值为4.31,酸雨污染比较严重;酸雨污染季节性明显,冬季酸雨出现频率高,影响范围广;酸雨的地域分布表现为以黔中为十字圆心,四个顶点遵义、都匀、安顺、凯里酸雨率高,而城市中心区酸雨污染较城郊严重;全省的酸雨污染主要是煤烟型污染。  相似文献   

2.
谢小惠 《环境》2005,(Z1):119
一、概述 降水监测的目的是准确、及时地了解全国或某一个区域的酸雨污染现状和发展趁势,确定酸雨污染的范围和酸雨污染程度;掌握酸雨污染的主要污染组分和特征,为控制酸雨污染提供科学依据.当前,降水监测的项目有:降水量、PH、电导率、SO42-、NO3-、Cl-、F-、K+、Na+、Ca2+、Mg2+、NH4+等项目,有条件的情况下还监测有机酸(甲酸、乙酸).根据测得降水PH的大小确定是否属于酸雨,通常称PH<5.60的降水为酸雨.下面就酸雨的主要污染物作简单的分析.  相似文献   

3.
重庆市渝中区20年酸雨污染变化趋势及成因分析研究   总被引:2,自引:0,他引:2  
以重庆市渝中区降雨及大气监测数据为基础,对重庆市渝中区近二十年酸雨污染的变化趋势、降水中化学成分变化进行分析,并从致酸源、地理因素、气象因素等方面探讨了重庆市渝中区酸雨污染的主要成因.结果表明:重庆市渝中区酸雨污染不仅来自于本区,还受外区输入性污染影响,特殊的地理环境和不利的大气扩散条件加重了酸雨污染的程度;近年来降雨pH总体上升,酸雨污染有所减轻;酸雨污染由煤烟型污染向石油型污染转变.  相似文献   

4.
昆明地区酸雨时空分布及其成因初探   总被引:4,自引:0,他引:4  
对1995-1999年昆明地区降雨监测资料的分析,昆明地区酸雨主要为局 地污染引起的硫酸型酸雨,酸雨污染近五年呈明显上升趋势,在空间分布上,城区酸雨频率和强度均明显强于效县。  相似文献   

5.
近年来大连市的酸雨污染呈逐年加重趋势,根据2010年酸雨监测的结果,从酸雨频率、酸雨分布及离子组成三方面对大连市酸雨污染的现状进行了简要概述,并根据大连市的实际情况提出了酸雨污染的防治措施。  相似文献   

6.
1992~2012年福州市和厦门市酸雨变化特征及影响因素   总被引:2,自引:1,他引:1  
郑秋萍  王宏  陈彬彬  隋平  林文 《环境科学》2014,35(10):3644-3650
利用1992~2012年福州市和厦门市的酸雨观测资料、天气形势和大气污染物浓度资料,分析酸雨变化特征及酸雨可能的影响因素.结果表明,福州市非酸雨和酸雨频率分别为38.1%和61.9%,厦门市分别为40.6%和59.4%;福州市年均降水pH值在4.1~5.5之间,2007年之后酸雨污染减轻,厦门市2006年之后酸雨污染减轻;冬、春季节酸雨污染重,夏、秋季节酸雨污染轻.降水强度能改变降水的酸性程度;福州市在东南(SE)、西南(SW)、西(W)、西北(NW)风向下酸雨污染较严重,厦门市在东北(NE)、SW、W、NW风向下酸雨污染较重;变性冷高压下酸雨污染最重,台风(热带辐合带)及其外围的天气形势下酸雨污染最轻;福州市大气污染物SO2、NO2、PM10浓度与降水pH值呈负相关关系.  相似文献   

7.
江西省酸雨特征分析及预测模型   总被引:1,自引:0,他引:1  
文章利用江西省酸雨监测站观测资料,分析了江西省酸雨的影响因素和特征。结果表明,近年来江西省酸雨污染情况有所缓和.江西酸雨呈季节性的变化,夏季酸雨污染较轻,冬季酸雨污染较重.江西省全省都有酸雨污染,但污染程度分布不均。江西的吉安、宜春以及景德镇污染较严重,鹰潭、上饶和萍乡污染较轻。江西省降雨的pH值随降雨量的增加先减小再增大,毛毛雨、小雨和中雨的pH值较小,而大雨和暴雨的pH值较大。综合分析江西酸雨的pH值和酸雨率,利用傅里叶函数的原理给出江西酸雨频率和pH值的数学模型。由数学模型得到的计算值与实际值较好吻合,说明所建的数学模型可以用来预测江西酸雨的频率和pH值。利用江西酸雨数学模型对未来10年的江西酸雨的频率和pH值进行预测。  相似文献   

8.
南京市酸雨特征及变化趋势分析   总被引:4,自引:0,他引:4  
张群  郁晶  喻义勇 《环境科学与管理》2009,34(12):108-111,126
以南京市2004年-2008年降水监测数据为基础,对降水pH值、酸雨出现频率、阴阳离子组成进行了分段统计分析,探讨了南京市酸雨类型、变化规律及与气象环境关系,认为全市酸雨污染呈现减轻趋势。酸雨类型主要为硫酸型,酸雨污染秋季较严重,春季次之,冬、夏季相对较轻,其中9月份酸雨强度最强。降水中主要阳离子为Ca2+和NH4+阴离子则以SO4^2-为主。相对湿度与降水pH值呈负相关;风速与降水pH值呈显著的正相关。  相似文献   

9.
大连市酸雨污染特征及原因简析   总被引:1,自引:0,他引:1  
2008年大连市酸雨频率为36.9%,酸雨污染以硫酸型污染为主,但硝酸盐对酸雨的贡献相对较高,降水中对酸雨主要起中和作用的离子为钙离子及铵根离子。2003年-2008年来大连市降水酸度和酸雨频率呈逐年上升趋势,从各季节变化看,最高酸雨频率主要发生在夏季,降水中(Ca2^+NH4^+)/(SO4^-2+NO3^-)呈下降趋势,从而说明虽然大连市局地的二氧化硫和氮氧化物污染对降水酸度产生一定影响,但相比而言,空气中碱性颗粒物的减少.对大连市酸雨频率的升高影响更大;大连市酸雨污染受外来源的远距离输送影响的比例很大。  相似文献   

10.
珠江三角洲地区酸雨污染简析   总被引:15,自引:0,他引:15  
以珠江三角洲地区主要城市的降水常规监测数据资料为依据,简要分析了该地区降水酸度和酸雨频率年度变化情况,并对酸雨的危害进行了初步的探讨。研究结果表明:该地区酸雨污染依然严重,降水酸度与二氧化硫污染等因素有关,酸雨类型以硫酸型为主。   相似文献   

11.
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.  相似文献   

12.
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.  相似文献   

13.
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.  相似文献   

14.
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.  相似文献   

15.
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.  相似文献   

16.
RemovalofheavymetalsfromsewagesludgebylowcostingchemicalmethodandrecyclinginagricultureWuQitang,NyirandegePascasie,MoCehuiF...  相似文献   

17.
Single and joint effects of pesticides and mercury on soil urease   总被引:6,自引:3,他引:3  
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.  相似文献   

18.
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.  相似文献   

19.
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.  相似文献   

20.
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.  相似文献   

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