Biosolid-borne tetracyclines and sulfonamides in plants

Tetracyclines and sulfonamides used in human and animal medicine are released to terrestrial ecosystems from wastewater treatment plants or by direct manure application. The interactions between plants and these antibiotics are numerous and complex, including uptake and accumulation, phytometabolism, toxicity responses, and degradation in the rhizosphere. Uptake and accumulation of antibiotics have been studied in plants such as wheat, maize, potato, vegetables, and ornamentals. Once accumulated in plant tissue, organic contaminants can be metabolized through a sequential process of transformation, conjugation through glycosylation and glutathione pathways, and ultimately sequestration into plant tissue. While studies have yet to fully elucidate the phytometabolism of tetracyclines and sulfonamides, an in-depth review of plant and mammalian studies suggest multiple potential transformation and conjugation pathways for tetracyclines and sulfonamides. The presence of contaminants in the vicinity or within the plants can elicit stress responses and defense mechanisms that can help tolerate the negative effects of contaminants. Antibiotics can change microbial communities and enzyme activity in the rhizosphere, potentially inducing microbial antibiotic resistance. On the other hand, the interaction of microbes and root exudates on pharmaceuticals in the rhizosphere can result in degradation of the parent molecule to less toxic compounds. To fully characterize the environmental impacts of increased antibiotic use in human medicine and animal production, further research is essential to understand the effects of different antibiotics on plant physiology and productivity, uptake, translocation, and phytometabolism of antibiotics, and the role of antibiotics in the rhizosphere.     

Seasonal variation and factors influencing perchlorate in water,snow, soil and corns in Northeastern China

Seasonal variation and influencing factors of perchlorate in snow, surface soil, rain, surface water, groundwater and corn were studied. Seven hundreds and seventy samples were collected in different periods in Harbin and its vicinity, China. Perchlorate concentrations were analyzed by ion chromatography–electrospray mass spectrometry. Results indicate that fireworks and firecrackers display from the Spring Festival to the Lantern Festival (February 2, 2011–February 17, 2011) can result in the occurrence of perchlorate in surface soil and snow. Perchlorate distribution is affected by wind direction in winter. Melting snow which contained perchlorate can dissolve perchlorate in surface soil, and then perchlorate can percolate into groundwater so that perchlorate concentrations in groundwater increased in spring. Perchlorate concentrations in groundwater and surface water decrease after rainy season in summer. Groundwater samples collected in the floodplain areas of the Songhua River and the Ashi River contained higher perchlorate concentrations than that far away with the rivers. The corns have the ability to accumulate perchlorate.     

Correction to: Urban water and food security in this century and beyond: Resource-smart cities and residents

The urban world population will increase from 3 to 8.5 thousand million in the 21st century. Cities become hot spots of both demand for water and global food and for disposed used water and nutrients. Sustainability requires that resource flows through our cities are co-managed and connected to agriculture. Reduced use of harmful chemicals in consumer products facilitates treatment to a quality that allows reuse/recycling of water and nutrients. A solid and liquid waste hierarchy can assist in ordering measures. A novel flexible water balance can guide city infrastructure and keep toilet water separate. New water-saving equipment can substantially reduce water use without losing personal comfort. The combination of these new approaches ascertains access to safe urban water, and that recovered nutrients from cities can substitute half of chemical fertilisers needed in food production. Now, thousands of new cities and suburbs provide unique opportunities to develop resource-smart and sustainable flows.     

壬基酚及其短链聚氧乙烯醚在污泥和土壤中的存在和降解

壬基酚聚氧乙烯醚(NPnEO)是广泛使用的表面活性剂．在污水处理厂中会降解为具有内分泌干扰效应的短链产物和最终产物壬基酚(NP)。剩余污泥是其进入环境的重要途径。介绍了NP和短链NPnEO在污泥中的存在情况、污泥处理过程对其存在的影响、以及这些物质随污泥处置过程进入土壤后的降解。     

Abiotic degradation of chlorinated ethanes and ethenes in water

INTRODUCTION: Chlorinated ethanes and ethenes are among the most frequently detected organic pollutants of water. Their physicochemical properties are such that they can contaminate aquifers for decades. In favourable conditions, they can undergo degradation. In anaerobic conditions, chlorinated solvents can undergo reductive dechlorination. DEGRADATION PATHWAYS: Abiotic dechlorination is usually slower than microbial but abiotic dechlorination is usually complete. In favourable conditions, abiotic reactions bring significant contribution to natural attenuation processes. Abiotic agents that may enhance the reductive dechlorination of chlorinated ethanes and ethenes are zero-valent metals, sulphide minerals or green rusts. OXIDATION: At some sites, permanganate and Fenton's reagent can be used as remediation tool for oxidation of chlorinated ethanes and ethenes. SUMMARY: Nanoscale iron or bimetallic particles, due to high efficiency in degradation of chlorinated ethanes and ethenes, have gained much interest. They allow for rapid degradation of chlorinated ethanes and ethenes in water phase, but they also give benefit of treating dense non-aqueous phase liquid.     

非有机溶剂高聚物萃取分离测定水样中苯酚的研究

在酸性溶液中,利用聚乙二醇-4000对水样中的苯酚进行萃取．并在聚乙二醇-4000、氨-氯化铵缓冲体系里对萃取相中的苯酚定量测定。在实验条件下,水样中苯酚被聚乙二醇-4000定量萃取并被4氨基安替比林定量测定。该方法快速、简单、无毒、为水样中苯酚的分离测定提供了一种较好的方法。     

Enhanced experimental flexibility and control in ecotoxicological mesocosm experiments--a new outdoor and indoor pond and stream system

Scope The German Federal Environmental Agency has put into operation a new modular mesocosm system consisting of eight outdoor and eight indoor ponds and streams in order to investigate fate and effects of chemicals and municipal wastewater in aquatic ecosystems. General design and special characteristics are given to demonstrate the wide range of possibilities for experimental research. - General design. Each of the 16 streams with riffle and pool sections can be varied in length up to 106 m. The streams can be run as circular or flow-through systems at a flow velocity of 0.02 to 0.6 m/s. Physico-chemical standard parameters are measured on-line. The 16 ponds, which can be connected to the stream systems, are equipped with drainage and pore water-sampling devices for simulating processes in the littoral zone including influent and effluent ground water flow. Perspectives Since the highly flexible and controllable construction also allows treating a wide range of hydrological and ecological experiments external institutions are invited to submit proposals.     

地下水修复系统中释氧材料的改进及pH调控

在采用释氧材料的地下水污染修复系统中,释氧材料提供溶解氧的同时,往往造成体系pH的升高。针对这一问题,将过氧化钙(CaO2)、水泥、河沙、膨润土和KH2PO4按一定比例混合在一起制作了3种释氧材料,并在柱实验中观测了不同释氧材料对水体溶解氧(DO)及pH值的影响。实验数据表明,水泥对释氧材料的缓释作用明显,有助于保证释氧速率平稳,避免由于释氧材料反应过快所带来的高pH问题;在释氧材料中添加一定量KH2PO4(质量分数小于10%),可以起到缓冲体系pH值的作用,并且不会造成修复系统磷污染;电气石具有降低溶液高pH值的作用,以粒径为1～2 mm的电气石作缓冲介质可以将体系pH值由11.3降至10.2。     

Colloid characterization and in situ release in shallow groundwater under different hydrogeology conditions

Environmental Science and Pollution Research - Changes to groundwater hydrodynamics and chemistry can lead to colloid release that can have a major impact on the groundwater environment. To analyze...     

Detecting and Tracking Changes in Ozone Air Quality

This paper presents a statistical method for filtering out or moderating the influence of meteorological fluctuations on ozone concentrations. Use of this technique in examining trends in ambient ozone air quality is demonstrated with ozone data from a monitoring location in New Jersey. The results indicate that this method can detect changes in ozone air quality due to changes in emissions in the presence of meteorological fluctuations. This method can be useful in examining the effectiveness of regulatory initiatives in improving ozone air quality.     

Modeling and interpreting bioavailability of organic contaminant mixtures in subsurface environments

Bioavailability often controls the fate of organic contaminants in surface and subsurface aquatic environments. Bioavailability can be limited by sorption, mass transfer, and intrinsic biodegradation potential and can be further altered by the presence of other compounds. This paper reviews current perspectives on the processes influencing subsurface contaminant bioavailability, how these processes are modeled, and how the relative role of the various processes can be assessed through bioavailability indices. Although these processes are increasingly well understood, the use of sophisticated models and indices often are precluded by an inability to estimate the many parameters that are associated with complex models. Nonetheless, the proper representation of sorption, mass transfer, biodegradation, and co-solute effects can be critical in predicting bio-attenuation. The influence of these processes on contaminant fate is illustrated with numerical simulations for the simultaneous degradation of toluene (growth substrate) and trichloroethylene (nongrowth cometabolite) in hypothetical, aerobic, solid-water systems. The results show how the relative impacts on contaminant fate of the model's various component processes depends upon system conditions, including co-solute concentrations. Slow biodegradation rates increase the inhibition effects of a cometabolite and suppress the rate enhancement effects of a growth substrate. Irrespective of co-solute effects, contaminant fate is less sensitive to biodegradation processes in systems with strong sorption and slow desorption rates. Bioavailability indices can be used to relate these findings and to help identify appropriate modeling simplifications. In general, however, there remains a need to redefine such indices in order that bioavailability concepts can be better incorporated into site characterization, remediation design, and regulatory oversight.     

Food waste collection and recycling for value-added products: potential applications and challenges in Hong Kong

About 3600 tonnes food waste are discarded in the landfills in Hong Kong daily. It is expected that the three strategic landfills in Hong Kong will be exhausted by 2020. In consideration of the food waste management environment and community needs in Hong Kong, as well as with reference to the food waste management systems in cities such as Linköping in Sweden and Oslo in Norway, a framework of food waste separation, collection, and recycling for food waste valorization is proposed in this paper. Food waste can be packed in an optic bag (i.e., a bag in green color), while the residual municipal solid waste (MSW) can be packed in a common plastic bag. All the wastes are then sent to the refuse transfer stations, in which food waste is separated from the residual MSW using an optic sensor. On the one hand, the sorted food waste can be converted into valuable materials (e.g., compost, swine feed, fish feed). On the other hand, the sorted food waste can be sent to the proposed Organic Waste Treatment Facilities and sewage treatment works for producing biogas. The biogas can be recovered to produce electricity and city gas (i.e., heating fuel for cooking purpose). Due to the challenges faced by the value-added products in Hong Kong, the biogas is recommended to be upgraded as a biogas fuel for vehicle use. Hopefully, the proposed framework will provide a simple and effective approach to food waste separation at source and promote sustainable use of waste to resource in Hong Kong.     

有机磷通过弱透水层的迁移转化规律研究

在地下水超量开采区,上层劣质潜水可以越过弱透水层补给承压水.有机磷能否随水迁移进入深层地下水构成水质污染是极为关注的问题.采用施压条件下将一定浓度的有机磷溶液渗透通过粘性土柱的模拟实验,对有机磷在饱和粘性土层中降解转化的各种因子及其影响机制进行分析,探讨有机磷在弱透水层环境中的降解转化和迁移的规律.结果表明:(1)粘性...     

Effects of potassium alkalis and sodium alkalis on the dechlorination of o-chlorophenol in supercritical water

Effects of potassium alkalis and sodium alkalis on the dechlorination of o-chlorophenol (o-CP) in supercritical water (SCW) were studied in this paper under the conditions of 450 degrees C and 25 MPa. Experimental results indicated that the dechlorination of o-CP can be accelerated significantly by all alkalis investigated. The dechlorination of o-CP proceeded mainly via two pathways: hydrodechlorination and hydrolysis. Both of the two pathways can be promoted by alkalis, and the dechlorination of o-CP can be accelerated by both the cations and hydroxide ion dissociated from alkalis. The overall dechlorination of o-CP can be accelerated by cations via promoting the hydrodechlorination pathway, while, hydroxide ion via promoting the hydrolysis pathway. In addition, the hydrodechlorination can be accelerated faster by sodium alkalis than that by potassium ones, while, the hydrolysis can be promoted faster by potassium alkalis. This difference may be caused by the different charge density between potassium ion and sodium ion, and the different solubility and dissociation constant between potassium alkalis and sodium alkalis in SCW. Dechlorination of o-CP with addition of alkalis prior to supercritical water oxidation (SCWO) process not only can avoid the reactor corrosion caused by the generated hydrochloric acid in direct SCWO of o-CP, but also can reduce the formation of toxic chlorinated byproducts compared with direct SCWO process or SCWO of o-CP with addition of alkali.     

Small-scale variability of metals in soil and composite sampling

Soil pollution data is also strongly scattering at small scale. Sampling of composite samples, therefore, is recommended for pollution assessment. Different statistical methods are available to provide information about the accuracy of the sampling process. Autocorrelation and variogram analysis can be applied to investigate spatial relationships. Analysis of variance is a useful method for homogeneity testing. The main source of the total measurement uncertainty is the uncertainty arising from sampling. The sample mass required for analysis can also be estimated using an analysis of variance. The number of increments to be taken for a composite sample can be estimated by means of simple statistical formulae. Analytical results of composite samples obtained from different fusion procedures of increments can be compared by means of multiple mean comparison. The applicability of statistical methods and their advantages are demonstrated for a case study investigating metals in soil at a very small spatial scale. The paper describes important statistical tools for the quantitative assessment of the sampling process. Detailed results clearly depend on the purpose of sampling, the spatial scale of the object under investigation and the specific case study, and have to be determined for each particular case.     

Simulation model for biotransformation of xenobiotics and chemotaxis in soil columns

In this paper a model is presented which can be used to simulate the behaviour of xenobiotic chemicals in soil columns with respect to their physical and chemical properties. Terms describing biological transformation of xenobiotics are also included in the model. It incorporates microbial growth following Monod kinetics and a chemotactic response of the transforming bacteria towards the xenobiotic substrate. The model appeared to yield good simulations of an experiment by Van der Meer et al. (1987) who investigated the degradation of 1,2-dichlorobenzene in soil columns inoculated with Pseudomonas sp. strain P51. The behaviour and the fate of 1,4-dichlorobenzene as found by Kuhn et al. (1985) can also be simulated using this model but their results were also adequately simulated using a simple second order model. The results generated by the model correspond to kinetic parameters obtained in other studies. It is concluded that the model is a useful tool for the investigation of the activity of bacteria degrading xenobiotics in soil columns, provided that the microbial parameters can be determined in independent experiments, and that the active microbial mass in the soil can be measured.     

Determination of chemical warfare agents in soil and material samples

A gas Chromatographic method for the determination of phenylarsenic compounds (sternutators) and their metabolites in soil and material samples is described. The chemical warfare agents (CWA), but not their hydrolysis and oxidation products, can be detected with GC/ECD. After derivatization with thiols or dithiols, the sum of diphenylarsenic and phenylarsenic compounds can be determined with GC/ECD. The comparison of the analytical results with and without derivatization shows that the sternutators in the investigated samples are metabolized in part.     

The relationship between flow and bacteria in streams

A method is proposed to relate the statistics of in-stream bacteria concentrations to the surface-runoff fraction of stream flow. The parameters of this relationship include the characteristic concentration of bacteria in surface runoff and the characteristic concentration of bacteria in the base flow, and these parameters can be derived from synoptic bacteria and flow measurements. The effectiveness of the proposed method is demonstrated at several U.S. locations for both Escherichia coli and fecal coliform bacteria. Application of the proposed method at a particular location showed that the method can be used to identify the most effective bacteria source controls and that conventional application of the load-duration curve might lead to erroneous identification of target sources.     

Cocaine and metabolites in waste and surface water across Belgium

Cocaine abuse, a growing social problem, is currently estimated from population surveys, consumer interviews and crime statistics. A new approach based on the analysis of cocaine (COC) and metabolites, benzoylecgonine (BE) and ecgonine methyl ester (EME), in water samples was applied to 28 rivers and 37 waste water treatment plants in Belgium using solid-phase extraction and liquid chromatography coupled to tandem mass spectrometry. While EME was undetectable, COC and BE were detectable with concentrations ranging from <1 to 753 ng/L and <1 to 2258 ng/L, respectively. BE concentrations were employed to calculate the local amount of abused cocaine. The highest values (up to 1.8 g/day cocaine per 1000 inhabitants) were found in large cities and during weekends. The estimation of cocaine abuse through water analysis can be executed on regular basis without cooperation of patients. It also gives clear geographical information, while prevention campaigns can easily be implemented and evaluated.     

鼓泡反应器中液相络合催化同时脱硫脱硝的研究

在鼓泡反应器中考察了[Co(en)3]2+同时吸收去除SO2和NO的影响因素,实验结果表明,pH值和脱硫剂种类是影响乙二胺合钴同时脱除NO和SO2的最重要影响因素,烟气中的氧促进乙二胺合钴吸收NO和SO2,烟气中的SO2,CO2和NO2对乙二胺合钴吸收NO具有抑制作用。在实验条件温度为20℃,pH为13.0,[Co(en)3]2+浓度为0.025 mol/L,加入1 g NH3.H2O的脱硝率更好,连续吸收60 min,脱硝率均保持在93.5%,加入NaOH和NH3.H2O的脱硫效果最好。乙二胺合钴络合同时脱除NO和SO2完全可以在一个装置中完成。