基于多限量标准的县域尺度畜禽养殖适度规模及潜在规模估算——以安徽省为例

开展了不同限量标准下安徽省各县(市、区)的畜禽养殖适度规模及潜在规模估算。结果表明,不同限量标准下的畜禽养殖适度规模估算结果在空间上都呈现出从安徽省的西北部向东南部逐渐递减的趋势,但不同限量标准下的畜禽养殖适度规模估算结果存在差异。其中,畜禽养殖排泄物氮负荷量限量标准下的畜禽养殖适度规模估算结果最大,全省为15 781.33万头(以猪当量计,下同);畜禽养殖排泄物猪粪当量警报值限量标准下的畜禽养殖适度规模最小,全省为4 733.88万头。6种限量标准下的畜禽养殖潜在规模空间分布与畜禽养殖适度规模基本一致。畜禽养殖排泄物猪粪当量警报值限量标准下的畜禽养殖适度规模超限最严重,全省超限796.81万头,共有48个县(市、区)超限,其中超限最多的是肥西县(102.92万头),超限最少的是马鞍山市市辖区(0.29万头)。     

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)...     

我国畜禽养殖业引致的环境问题及主要对策

在阐述目前畜禽养殖业引致的主要环境问题及其与可持续发展关系的基础上 ,从生态系统学的角度提出应强化规模化畜禽养殖废弃物的综合利用 ,开展固体废弃物和污水治理等相关领域的研究 ,进一步做好畜禽养殖污染防治工作 ,有效地保护和改善农村生态环境 ,以期促进畜禽养殖环境与经济的协调发展。     

我国畜禽养殖业引致的环境问题及主要对策

在阐述目前畜禽养殖业引致的主要环境问题及其与可持续发展关系的基础上，从生态系统学的角度提出应强化规模化畜禽养殖废弃物的综合利用，开展固体废弃物和污水治理等相关领域的研究，进一步做好畜禽养殖污染防治工作，有效地保护和改善农村生态环境，以期促进畜禽养殖环境与经济的协调发展。     

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。     

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。     

启东市畜禽养殖污染调查及防治对策思考

根据启东市第一次全国污染源普查数据,对启东市畜禽养殖污染的现状和成因进行了深入分析,并提出了对畜禽养殖污染防治的对策思考。     

规模化养殖场畜禽粪便发酵还田负荷估算及风险评价——以四川省邛崃市为例

以邛崃市为研究对象,结合其规模化畜禽养殖量、畜禽粪便排放量以及农作物氮肥需求量等,对研究区域耕地畜禽粪便最大氮负荷量进行了估算,将其与畜禽粪便发酵副产物沼渣沼液还田产生的实际氮负荷量进行比较,由此对现有养殖规模下的环境风险进行了评价.结果表明,当前邛崃市除孔明乡、火井镇、回龙镇受到沼渣沼液还田污染以外,其他各养殖区域沼渣沼液还田尚未造成明显污染.因此,邛崃市规模化养殖还存在较大的发展空间,但必须从实际出发,合理规划,才能实现农业和环境的可持续发展.     

畜禽养殖污染防治典型工程的综合效益评价

通过对我国畜禽养殖污染防治工程建设现状的调查和分析,拟定了我国畜禽养殖污染防治工程的评价指标体系,采用层次分析与灰色关联度分析相结合的综合评价方法,对国内的8个典型工程的综合效益进行了评价。评价结果表明,规模化及综合性的养殖污染防治工程可获得较好的综合效益,而在养殖污染防治中采用单一的沼气化处理,由于其经济性较差,目前尚不能获得较好的综合效益。     

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.     

Dioxin- and POP-contaminated sites—contemporary and future relevance and challenges

BACKGROUND, AIM AND SCOPE: Once they have been generated, polychlorinated dibenzo-p-dioxins (PCDDs) and dibenzofurans (PCDFs) and other persistent organic pollutants (POPs) can persist in soils and sediments and in waste repositories for periods extending from decades to centuries. In 1994, the US EPA concluded that contaminated sites and other reservoirs are likely to become the major source of contemporary pollution problems with these substances. With this in mind, this article is the first in a new series in ESPR under the title 'Case Studies on Dioxin and POP Contaminated Sites--Contemporary and Future Relevance and Challenges', which will address this important issue. The series will document various experiences from sites contaminated with PCDD/F and other POPs. This article provides an overview of the content of the articles comprising the series. In addition, it provides a review of the subject in its own right and identifies the key issues arising from dioxin/POP-contaminated sites. Additionally, it highlights the important conclusions that can be drawn from these examples. The key aim of this article and of the series as a whole is to provide a comprehensive overview of the types of PCDD/F contaminated sites that exist as a result of historical activities. It details the various processes whereby these sites became contaminated and attempts to evaluate their contemporary relevance as sources of PCDD/Fs and other POPs. It also details the various strategies used to assess these historical legacies of contamination and the concepts developed, or which are under development, to effect their remediation. MAIN FEATURES: Special sessions on 'Contaminated sites--Cases, remediation, risk and policy' were held at the DIOXIN conferences in 2006 and 2007, and this theme will be continued at DIOXIN 2008 to be held in Birmingham. Selected cases from the approximately 70 contributions made to these sessions, together with some additional invited case studies are outlined together with the key issues they raise. By evaluating these cases and adding details of experiences published in the current literature, an overview will be given of the different features and challenges of dioxin and POP-contaminated sites. RESULTS: This article provides a systematic categorisation of types of PCDD/F and POP-contaminated sites. These are categorised according to the chemical or manufacturing process, which generated the PCDD/Fs or POPs and also includes the use and disposal aspects of the product life cycle in question. The highest historical PCDD/F and dioxin-like polychlorinated biphenyl (PCB) contamination burdens have arisen as a result of the production of chlorine and of chlorinated organic chemicals. In particular, the production of chlorinated pesticides, PCBs and the related contaminated waste streams are identified being responsible for historical releases of toxic equivalents (TEQs) at a scale of many tonnes. Along with such releases, major PCDD/F contaminated sites have been created through the application or improper disposal of contaminated pesticides, PCBs and other organochlorine chemicals, as well through the recycling of wastes and their attempted destruction. In some extreme examples, PCDD/F contaminated sites have also resulted from thermal processes such as waste incinerators, secondary metal industries or from the recycling or deposition of specific waste (e.g. electronic waste or car shredder wastes), which often contain chlorinated or brominated organic chemicals. The examples of PCDD/F and dioxin-like PCB contamination of fish in European rivers or the impact of contaminated sites upon fishing grounds and upon other food resources demonstrate the relevance of these historical problems to current and future human generations. Many of the recent food contamination problems that have emerged in Europe and elsewhere demonstrate how PCDD/F and dioxin like PCBs from historical sources can directly contaminate human and animal feedstuffs and indeed highlight their considerable contemporary relevance in this respect. Accordingly, some key experiences and lessons learnt regarding the production, use, disposal and remediation of POPs from the contaminated sites are summarised. DISCUSSION: An important criterion for evaluating the significance and risks of PCDD/Fs and other POPs at contaminated sites is their present or future potential for mobility. This, in turn, determines to a large degree their propensity for off-site transport and environmental accessibility. The detailed evaluation of contaminated site cases reveals different site-specific factors, which influence the varied pathways through which poor water-soluble POPs can be mobilised. Co-contaminants with greater water solubility are also typically present at such sites. Hence, pumping of groundwater (pump and treat) is often required in addition to attempting to physically secure a site. At an increasing number of contaminated sites, securing measures are failing after relatively short time spans compared to the time horizon, which applies to persistent organic pollutant contamination. Due to the immense costs and challenges associated with remediation of contaminated sites 'monitored natural attenuation' is increasingly gaining purchase as a conceptual remediation approach. However, these concepts may well prove limited in their practical application to contaminated sites containing persistent organic pollutants and other key pollutants like heavy metals. CONCLUSIONS: It is inevitable, therefore, that dioxin/POP-contaminated sites will remain of contemporary and future relevance. They will continue to represent an environmental issue for future generations to address. The securing and/or remediation of dioxin/POP-contaminated sites is very costly, generally in the order of tens or hundreds of millions of dollars. Secured landfills and secured production sites need to be considered as constructions not made for 'eternity' but built for a finite time scale. Accordingly, they will need to be controlled, supervised and potentially repaired/renewed. Furthermore, the leachates and groundwater impacted by these sites will require ongoing monitoring and potential further remediation. These activities result in high maintenance costs, which are accrued for decades or centuries and should, therefore, be compared to the fully sustainable option of complete remediation. The contaminated site case studies highlight that, while extensive policies and established funds for remediation exist in most of the industrialised western countries, even these relatively well-regulated and wealthy countries face significant challenges in the implementation of a remediation strategy. This highlights the fact that ultimately only the prevention of contaminated sites represents a sustainable solution for the future and that the Polluter Pays Principle needs to be applied in a comprehensive way to current problems and those which may emerge in the future. RECOMMENDATIONS AND PERSPECTIVES: With the continuing shift of industrial activities in developing and transition economies, which often have poor regulation (and weak self-regulation of industries), additional global challenges regarding POPs and other contaminated sites may be expected. In this respect, a comprehensive application of the "polluter pays principle" in these countries will also be a key to facilitate the clean-up of contaminated areas and the prevention of future contaminated sites. The threats and challenges of contaminated sites and the high costs of securing/remediating the problems highlight the need for a comprehensive approach based upon integrated pollution prevention and control. If applied to all polluting (and potentially polluting) industrial sectors around the globe, such an approach will prove to be both the cheapest and most sustainable way to underpin the development of industries in developing and transition economies.     

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.     

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.     

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.     

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...     

畜禽养殖业污染与循环经济

解决畜禽养殖业的污染问题要以充分利用资源为根本出发点，通过对污染全过程控制及废物综合利用，达到畜禽粪便的减量化、无害化、资源化，走循环经济的发展道路。     

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.     

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.