北京市畜禽养殖业污染治理模式探讨

由于北京市农业耕地资源有限、规模化养殖场集中、畜禽养殖业管理薄弱等原因,致使大量畜禽粪便随意排放和流失,破坏生态环境。为解决北京市畜禽养殖业污染问题,在概述畜禽粪污处理技术的基础上,根据北京市畜禽养殖业污染治理现状,分析其存在的主要问题,探讨了基于区域集中式粪污处理模式,并提出了相关规划与政策建议,为北京市畜禽养殖污染治理提供经济、可行的发展方向。     

新西兰氮排放配额与交易制度对中国的启示——以奶牛养殖业为例

近年来,排污权有偿使用与交易制度在中国部分省份开展了试点工作,许多大型的规模化畜禽养殖场也进行了排污许可证的申领。针对新西兰奶牛养殖业的污染治理措施进行了研究,梳理其开展污染防治工作的措施体系,以陶泊湖周边施行的氮排放配额与交易为主要对象,阐述了新西兰在养殖业排放配额与交易制度方面的工作实践,其配额基准核定方法、"资源许可证"申领制度、配额交易体系、相关支撑措施在一定程度上具备优势和先进性,对中国的畜禽养殖污染减排工作具有借鉴意义。     

宝应县畜禽养殖业的现状调研及污染防治对策

调查了宝应县畜禽养殖业的发展现状及分布情况,阐述了该县畜禽养殖业的污染防治状况,分析了污染防治中存在的主要问题,并提出了当地畜禽养殖业污染防治的基本思路和治理措施,对贯彻落实防治措施提出了建议。     

畜禽规模养殖污染治理项目管理机制研究——以上海市为例

对上海市二十余年畜禽养殖污染治理实践经验和启示进行回顾与评价,探讨了当前畜禽规模养殖污染治理项目的管理需求,并结合上海市"十二五"期间畜禽规模养殖污染现状特征及减排形势,研究了适于畜禽规模养殖污染治理的项目管理机制,包括项目实施管理和工程建成运行监管,为工程推进实施和长效稳定运行提供技术保障,确保其长期发挥生态环境效益。     

军山湖流域农业非点源污染氮、磷入湖负荷估算

参照国内外相关湖泊研究的方法,在开展流域调查的基础上,按照畜禽养殖污染、农业种植业流失、水产养殖污染和农村生活污染4类途径,结合各乡镇流域面积所占比例、污染源产生量、排放系数和流失系数等估算了军山湖流域农业非点源污染氮、磷的入湖负荷.结果表明,农业种植业流失和畜禽养殖污染是军山潮流域农业非点源污染入湖氮的主要来源,分别占入湖氮总量的37.5％和34.7％,其次为水产养殖污染,占23.2％;畜禽养殖污染是入湖磷的主要来源,占50.8％,其次为农业种植业流失和水产养殖污染,分别占24.4％和20.0％;农村生活污染对入湖氮、磷的贡献率最小.     

清江流域水环境面源污染源强核算及主要环境问题分析

清江是湖北省境内最大的一条长江支流,为及时掌握和控制流域内日益严重的面源污染问题,对清江流域水环境面源污染进行匡算。通过对计算结果的分析,得出该区域农田径流和畜禽养殖为重要面源污染源,恩施段,建始段、长阳段和宜都段是清江流域面源污染控制重点区域。农田径流污染主要与当地水土流失严重,土地利用方式不合理,及化肥施用量较大有关。畜禽养殖污染主要由分散式养殖、畜禽粪尿无序排放引起。面源污染控制重点区域内的环境问题与当地经济水平、人口密度和国土面积有关。     

郊区规模化畜禽养殖对环境的潜在污染分析

郊区畜禽养殖对环境的污染越来越严重.以国内某城市周边畜禽养殖业为例,通过确定主要畜禽(猪、牛、鸡、羊)污染物的产污系数,估算了2009年北方某城市各区县的主要畜禽粪污中COD、TN、TP含量,分别约为1.1×106、5.4×104、9×103 t.在不同区县中,G区单位耕地面积N、P负荷最大,分别为309.5、52.7 kg/hm2,远远超出土壤的消纳能力;在靠海的主要3个区(A、B、C区)中,其中C区的畜禽粪污对水体潜在污染负荷最高,COD、TN、TP分别达4 858.4、252.4、47.9t,可能造成水质的污染.     

畜禽养殖污染物排放及防治对策

在分析畜禽养殖对水环境污染的严重性后,提出了防治畜禽养殖污染的对策措施。     

UASB-SBR组合工艺处理畜禽养殖废水的研究

近年来,随着中国畜禽养殖业的快速发展,落后的养殖模式和污染防治设施,使畜禽养殖污染日趋严重,畜禽养殖污染已居农业污染源之首,已成为中国环境污染的重要因素,对环境质量乃至人体健康都会产生不良影响。文中采用UASB—SBR组合工艺处理畜禽养殖废水,通过试验探讨SBR反应器启动方法及最佳运行模式,同时研究UASB反应器的启动方法。结果表明,SBR运行的最佳模式为进水0.5 h、反应8 h、沉淀1 h、出水0.5 h、闲置14 h。经过一段时间的启动,UASB和SBR反应器均成功启动,UASB—SBR组合工艺在处理畜禽养殖废水时可获得稳定的处理效果,COD、氨氮、总磷等出水水质均达到《畜禽养殖业污染物排放标准》(GB18596-2001)要求,为畜禽养殖废水处理的工程化应用提供了参考依据。     

UV/H2O2联合氧化法去除畜禽养殖废水中抗生素

随着畜禽养殖业的迅猛发展,畜禽养殖废水污染问题日益突出,尤其是养殖过程中大量使用抗生素,致使畜禽养殖废水含有抗生素,成为一类新型环境危害污染物.如何有效去除畜禽养殖废水中的抗生素,成为国内外研究热点.采用UV/H2O2联合氧化法去除畜禽养殖废水中抗生素(磺胺甲恶唑、磺胺噻唑、磺胺甲噻二唑、磺胺二甲氧嘧啶、磺胺二甲嘧啶)...     

Sorption and desorption of Cu and Cd by macroalgae and microalgae

The sorption and desorption of Cu and Cd by two species of brown macroalgae and five species of microalgae were studied. The two brown macroalgae, Laminaria japonica and Sargassum kjellmanianum, were found to have high capacities at pHs between 4.0 and 5.0 while for microalgae, optimum pH lay at 6.7. The presence of other cations in solution was found to reduce the sorption of the target cation, suggesting a competition for sorption sites on organisms. Sorption isotherms obeyed the Freundlich equation, suggesting involvement of a multiplicity of mechanisms and sorption sites. For the microalgae tested, Spirulina platensis had the highest capacity for Cd, followed by Nannochloropsis oculata, Phaeodactylum tricornutum, Platymonas cordifolia and Chaetoceros minutissimus. The reversibility of metal sorption by macroalgae was examined and the results show that both HCl and EDTA solutions were very effective in desorbing sorbed metal ions from macroalgae, with up to 99.5% of metals being recovered. The regenerated biomass showed undiminished sorption performance for the two metals studied, suggesting the potential of such material for use in water and wastewater treatment.     

Kinetic and structural relationships of transition monomeric and oligomeric carboxyl- and choline-esterases

The kinetic and structural relationships of eight electrophoretically pure mammalian serum and liver serine carboxylesterases (CE) and cholinesterases (ChE) have been studied. Eight CE's and ChE's, which were fully resolved but only partially purified, provided additional information. Five of the electrophoretically pure esterases were monomeric, and of these, four belonged to a new and widely distributed class. These four monomeric esterases hydrolyzed choline esters, but at widely differing rates. Thus two were termed monomeric butyrylcholinesterases, mBuChE I and II, and two were monomeric CE's (mCE). The rabbit liver mCE was not a subunit of the oligomeric CE (oCE), although the oCE also hydrolyzed choline esters at a very low rate. The complex kinetics of the mCE's, mBuChE's, oCE's, and of the oligomeric BuChE's of horse and human serum could be interpreted according to a single reaction scheme involving an allosteric site and the equation derived from it. Thus activation and inhibition at high substrate concentrations, together with sigmoidal activity versus substrate concentration plots, all of which characterize the reactions of these esterases, could be interpreted by a single scheme and equation. Structural and kinetic comparisons showed a progressive transition of properties from the oCE's through the mCE's to the oBuChE's. One of the purified mCE's was from horse serum, and it exhibited physical and kinetic properties unlike those of the liver mCE's or oCE's.     

Persistence and dissipation kinetics of trifloxystrobin and tebuconazole in onion and soil

The persistence and dissipation kinetics of trifloxystrobin and tebuconazole on onion were studied after application of their combination formulation at a standard and double dose of 75 + 150 and 150 + 300 g a.i. ha^?1. The fungicides were extracted with acetone, cleaned-up using activated charcoal (trifloxystrobin) and neutral alumina (tebuconazole). Analysis was carried out by gas chromatograph (GC) and confirmed by gas chromatograph mass spectrometry (GC-MS). The recovery was above 80% and limit of quantification (LOQ) 0.05 mg kg^?1 for both fungicides. Initial residue deposits of trifloxystrobin were 0.68 and 1.01 mg kg^?1 and tebuconazole 0.673 and 1.95 mg kg^?1 from standard and double dose treatments, respectively. Dissipation of the fungicides followed first-order kinetics and the half life of degradation was 6–6.6 days. Matured onion bulb (and field soil) harvested after 30 days was free from fungicide residues. These findings suggest recommended safe pre-harvest interval (PHI) of 14 and 25 days for spring onion consumption after treatment of Nativo 75 WG at the standard and double doses, respectively. Matured onion bulbs at harvest were free from fungicide residues.     

Sorption and Desorption Behavior of Chloroanilines and Chlorophenols on Montmorillonite and Kaolinite

The bioavailability of pollutants, pesticides and/or their degradation products in soil depends on the strength of their sorption by the different soil components, particularly by the clay minerals. This study reports the sorption-desorption behavior of the environmentally hazardous industrial pollutants and certain pesticides degradation products, 3-chloroaniline, 3,4-dichloroaniline, 2,4,6-trichloroaniline, 4-chlorophenol, 2,4-dichlorophenol and 2,4,6-trichlorophenol on the reference clays kaolinite KGa-1 and Na-montmorillonite SWy-l. In batch studies, 2.0 g of clay were equilibrated with 100.0 mL solutions of each chemical at concentrations ranging from 10.0 to 200.0 mg/L. The uptake of the compounds was deduced from the results of HPLC-UV-Vis analysis. The lipophilic species were best retained by both clay materials. The most lipophilic chemical used in the study, 2,4,6-trichloroaniline, was also the most strongly retained, with sorption of up to 8 mg/g. In desorption experiments, which also relied on HPLC-UV-Vis technique, 2,4,6-trichloroaniline was the least desorbed from montmorillonite. However, on kaolinite all of the compounds under study were irreversibly retained. The experimental data have been modelled according to the Langmuir and Freundlich isotherms. A hypothesis is proposed concerning the sorption mechanism and potential applications of the findings in remediation strategies have been suggested.     

Sorption and desorption behavior of chloroanilines and chlorophenols on montmorillonite and kaolinite

The bioavailability of pollutants, pesticides and/or their degradation products in soil depends on the strength of their sorption by the different soil components, particularly by the clay minerals. This study reports the sorption-desorption behavior of the environmentally hazardous industrial pollutants and certain pesticides degradation products, 3-chloroaniline, 3,4-dichloroaniline, 2,4,6-trichloroaniline, 4-chlorophenol, 2,4-dichlorophenol and 2,4,6-trichlorophenol on the reference clays kaolinite KGa-1 and Na-montmorillonite SWy-l. In batch studies, 2.0 g of clay were equilibrated with 100.0 mL solutions of each chemical at concentrations ranging from 10.0 to 200.0 mg/L. The uptake of the compounds was deduced from the results of HPLC-UV-Vis analysis. The lipophilic species were best retained by both clay materials. The most lipophilic chemical used in the study, 2,4,6-trichloroaniline, was also the most strongly retained, with sorption of up to 8 mg/g. In desorption experiments, which also relied on HPLC-UV-Vis technique, 2,4,6-trichloroaniline was the least desorbed from montmorillonite. However, on kaolinite all of the compounds under study were irreversibly retained. The experimental data have been modelled according to the Langmuir and Freundlich isotherms. A hypothesis is proposed concerning the sorption mechanism and potential applications of the findings in remediation strategies have been suggested.     

Bacterial and archaeal diversity in oil fields and reservoirs and their potential role in hydrocarbon recovery and bioprospecting

Environmental Science and Pollution Research - Hydrocarbon is a primary source of energy in the current urbanized society. Considering the increasing demand, worldwide oil productions are declining...     

Isocyanatocyclohexane and isothiocyanatocyclohexane levels in urban and industrial areas and possible emission-related activities

Isocyanatocyclohexane and isothiocyanatocyclohexane are becoming relevant compounds in urban and industrial air, as they are used in important amounts in automobile industry and building insulation, as well as in the manufacture of foams, rubber, paints and varnishes. Glass multi-sorbent tubes (Carbotrap, Carbopack, Carboxen) were connected to LCMA-UPC pump samplers for the retention of iso- and isothiocyanatocyclohexanes. The analysis was performed by automatic thermal desorption (ATD) coupled with capillary gas chromatography (GC)/mass spectrometry detector (MSD). TD-GC/MS was chosen as analytical method due to its versatility and the possibility of analysis of a wide range of volatility and polarity VOC in air samples. The method was satisfactory sensitive, selective and reproducible for the studied compounds. The concentrations of iso- and isothioisocyanatocyclohexanes were evaluated in different urban, residential and industrial locations from extensive VOC air quality and odour episode studies in several cities in the Northeastern edge of Spain. Around 200–300 VOC were determined qualitatively in each sample. Higher values of iso- and isothiocyanatocyclohexane were found in industrial areas than in urban or residential locations. The concentrations ranged between n.d.−246 and n.d.−29 μg m⁻³ for isocyanatocyclohexane and isothiocyanatocyclohexane, respectively, for industrial areas. On the other hand, urban and residential locations showed concentrations ranging between n.d.−164 and n.d.−29 μg m⁻³ for isocyanatocyclohexane and isothiocyanatocyclohexane, respectively. The site location (urban or industrial), the kind and nearness of possible iso- and isothiocyanatocyclohexane emission activities (industrial or building construction) and the changes of wind regimes throughout the year have been found the most important factors influencing the concentrations of these compounds in the different places.     

Degradation in soil and water and ecotoxicity of rimsulfuron and its metabolites.

The degradation and ecotoxicity of sulfonylurea herbicide rimsulfuron and its major metabolites were examined in batch samples of an alluvial sandy loam and in freshwater. An HPLC-DAD method was adapted to simultaneously identify and quantify rimsulfuron and its metabolites, which was successfully validated by GC-MS analysis. In aqueous solutions, pure rimsulfuron was rapidly hydrolyzed into metabolite 1 (N-(4,6-dimethoxypyrimidin-2-yl)-N-(3-(ethylsulfonyl)-2-pyridinylurea)), which itself was transformed into the more stable metabolite 2 (N-((3-(ethylsulfonyl)-2-pyridinyl)-4,6-dimethoxy-2-pyrimidineamine)), with half-life (t(1/2)) values of 2 and 2.5 days, respectively. Hydrolysis was instantaneous under alkaline conditions (pH = 10). In aqueous suspensions of the alluvial soil (pH = 8), formulated rimsulfuron had a half-life of 7 days, whereas that of metabolite 1 was similar to that in water (about 3.5 days). The degradation of the two major metabolites was also studied in soil suspensions with the pure compounds at concentrations ranging from 1 to 10 mg l(-1). The half-life of metabolite 1 ranged from 3.9 to 5 days, close to the previous values. Metabolite 2 was more persistent and its degradation is strongly dependent on the initial concentration (C0): half-life values ranged from 8.1 to 55 days at 2-10 mg l(-1), respectively. These values are higher than those determined from the kinetics of metabolite 1 transformation into metabolite 2 (t(1/2) = 8-19 days). The ecotoxicity of the three chemicals was evaluated through their effect on Daphnia magna and Vibrio fischeri (Microtox bioassay). No effect was observed on D. magna with 24 and 48 h acute toxicity tests. Similarly, no toxic effect was observed with the Microtox test for the three chemicals in the range of concentrations tested that included the field application dose. Thus, being of low persistence and lacking acute toxicity, these chemicals present a low environmental risk. However, chronic effects should be studied in order to confirm the safety of rimsulfuron and its major metabolites.     

Sources and fate of PCDD and PCDF

PCDD and PCDF were found in urban air particulates from St. Louis and Washington, D.C., and in sediments from the Great Lakes and Siskiwit Lake, Isle Royale. The similarity between the PCDD and PCDF found in air particulates and sediment samples and the presence of PCDD and PCDF in sediment from Siskiwit Lake (a location which can receive only atmospheric inputs) suggest that these compounds are emitted to the atmosphere from combustion sources. The historical input of PCDD and PCDF to dated sediment cores shows a strong increase since 1940, and this suggests that the incineration of chlorinated organic compounds is an important source of PCDD and PCDF to the environment.