Extraction and purification of DNA from phytopathogenic soil-inhabiting Fusarium species

Working quantities of good quality DNA was obtained from three pathogenic forms of the soil-inhabiting fungus, Fusarium oxysporum (FO), which causes economically significant diseases in tomato crops. The mitochondrial, nuclear and ribosomal fractions from each of the DNAs were separated by cesium chloride gradient centrifugations. The data suggest a decrease in nuclear DNA and an increase in mitochondrial DNA correlated with increasing pathogenicity among the three pathogens examined. Ribosomal DNA was detected only in FO, the least pathogenic form.     

Identifying the fouling behavior of forward osmosis membranes exposed to different inorganic components with high ionic strength

Environmental Science and Pollution Research - Functionalized multiwalled carbon nanotube (f-MWCNT) mixed matrix forward osmosis (FO) membranes were fabricated by phase inversion, and the mechanism...     

基于海水和盐田水的正渗透驱动液

采用海水和盐田水作为驱动液,研究正渗透过程中的通量变化和膜污染特征,探索其作为驱动液的可行性。结果表明,海水和盐田水含有大量的盐离子,具有高的渗透压,海水、2#、5#和9#盐田水与0.42、0.8、2.2和4.2 mol/L的氯化钠具有同样的通量行为。随海水和盐田水浓度增加,通量增加,同时污染也越严重。扫描电子显微镜观察和荧光光谱分析发现,盐田水中的硅酸盐和有机物会沉积在膜表面,引起比较严重的膜污染,尤其是高浓度的盐田水。海水和盐田水作为正渗透过程中的驱动液需要进行一定的预处理。     

Biochar as low-cost sorbent of volatile fuel organic compounds: potential application to water remediation

Pyrolysis of waste materials to produce biochar is an excellent and suitable alternative supporting a circular bio-based economy. One of the properties attributed to biochar is the capacity for sorbing organic contaminants, which is determined by its composition and physicochemical characteristics. In this study, the capacity of waste-derived biochar to retain volatile fuel organic compounds (benzene, toluene, ethylbenzene and xylene (BTEX) and fuel oxygenates (FO)) from artificially contaminated water was assessed using batch-based sorption experiments. Additionally, the sorption isotherms were established. The results showed significant differences between BTEX and FO sorption on biochar, being the most hydrophobic and non-polar contaminants those showing the highest retention. Furthermore, the sorption process reflected a multilayer behaviour and a relatively high sorption capacity of the biochar materials. Langmuir and Freundlich models were adequate to describe the experimental results and to detect general differences in the sorption behaviour of volatile fuel organic compounds. It was also observed that the feedstock material and biochar pyrolysis conditions had a significant influence in the sorption process. The highest sorption capacity was found in biochars produced at high temperature (>?400 °C) and thus rich in aromatic C, such as eucalyptus and corn cob biochars. Overall, waste-derived biochar offers a viable alternative to be used in the remediation of volatile fuel organic compounds from water due to its high sorption capacity.

     

Treatment of reactive dyes and textile finishing wastewater using Fenton's oxidation for reuse

Fenton's oxidation (FO) was used to decolourise and degrade some reactive dyes (Remazol Black 5, Remazol Red, Remazol Blue, Remazol Yellow) and raw textile finishing industry effluents (S1, S2, S3) containing mainly reactive dyes. The operational conditions for pH varied between 2.5 and 4.0 while temperature ranged from 30°C to 50°C. The concentrations of FeSO₄ and H₂O₂ varied to a wide range (200–600 mg/l of FeSO₄, 300–1000 mg/l of H₂O₂) depending on the type of the dyes and their mixture and textile additives used in the process. FO is highly effective for colour removal (>99%) for reactive dyes and (87–94%) for textile finishing wastewater. It can be applied as a pretreatment and the remaining total dissolved solids (TDS) can be removed by an additional advanced process, e.g. membrane process.     

Modelling of stomatal conductance and ozone flux of Norway spruce: comparison with field data

It has been proposed that stomatal flux of ozone would provide a more reliable basis than ozone exposure indices for the assessment of the risk of ozone damage to vegetation across Europe. However, implementation of this approach requires the development of appropriate models which need to be rigorously tested against actual data collected under field conditions. This paper describes such an assessment of the stomatal component of the model described by Emberson et al. (2000. Modelling stomatal ozone flux across Europe. Environmental Pollution 110). Model predictions are compared with field measurements of both stomatal conductance (g(s)) and calculated ozone flux for shoots of mature Norway spruce (Picea abies) growing in the Tyrol Mountains in Austria. The model has been developed to calculate g(s) as a function of leaf phenology and four environmental variables: photosynthetic flux density (PFD), temperature, vapour pressure deficit (VPD) and soil moisture deficit (SMD). The model was run using climate data measured on site, although the SMD component was omitted since the necessary data were not available. The model parameterisation for Norway spruce had previously been collected from the scientific literature and therefore established independently from the measurement study. Overall, strong associations were found between model predictions and measured values of stomatal conductance to ozone (GO(3)) and calculated stomatal ozone flux (FO(3)). Average diurnal profiles of GO(3) and FO(3) showed good agreement between the field data and modelled values except during the morning period of 1990. The diurnal pattern of ozone flux was determined primarily by PFD and VPD, as there was little diurnal variation in ozone concentration. In general, the model predicted instances of high ozone flux satisfactorily, indicating its potential applicability in identifying areas of high ozone risk for this species.     

Inverse modeling to estimate LNAPL plume release timing

Methodologies are presented for dating releases of light nonaqueous phase liquids (LNAPLs) using an inverse modeling approach with simple analytical models. Models for LNAPL plume migration are presented to predict LNAPL plume velocity in the unsaturated and saturated zones as a function of basic soil and fluid properties. A relative mobility factor is introduced for LNAPL movement at the water table that depends primarily on the van Genuchten n parameter (related to the breadth of the soil pore size distribution) and the magnitude of water table fluctuations. Estimated LNAPL plume velocities compare reasonably with more rigorous numerical models, which may be used in cases where data availability warrant the greater effort entailed.Two methods of estimating release timing and its uncertainty are investigated. A direct estimation method is described that determines travel time for a single observed travel distance based on estimated soil and fluid properties. Release date uncertainty may be determined using the first order (FO) or Monte Carlo (MC) methods. The second method for estimating release date involves nonlinear parameter estimation utilizing distance vs. time measurements and other data.A case study is presented for a field site where independent estimates of release timing were obtained from a numerical modeling analysis. Release timing estimates based on direct inversion of the analytical timing model agree well with the numerical analysis. Results for a second field site indicate that release date confidence limits estimated by the FO method, assuming log-normally distributed travel times, are close to values determined by the MC method, which makes no assumption regarding the form of the travel time probability distribution.Results for a hypothetical problem indicate that LNAPL velocity and travel time may be accurately estimated if sufficient data on travel distance vs. time are available. Incorporating prior information on relevant soil and fluid properties into the objective function reduces the uncertainty in release date if prior estimates are accurate. However, biased prior estimates may lead to over- or underestimation of release date uncertainty. Simultaneous estimation of soil and fluid properties and release date is possible if prior information is available to condition the parameter estimates.     

The anaerobic biodegradability of municipal sludge and fat, oil, and grease at mesophilic conditions.

The anaerobic biodegradability of municipal primary and secondary sludge with increasing levels of partially dewatered fat, oil, and grease (FOG) was assessed using a mixed methanogenic culture at 35 "C. Under batch conditions with an acclimated and enriched microbial population, the sludge loading was 3 kg volatile solids/m3 and the highest FOG loading tested was 1.5 kg volatile solids/m3, resulting in a methane yield of 245 mL methane/g sludge volatile solids added at 35 degrees C and 1010 mL methane/g FOG volatile solids added at 35 degrees C. Under semicontinuous feeding conditions, the sludge and sludge plus FOG loading tested were 3 and 3.75 kg volatile solids/m3-d, respectively. Within 23 days of operation, the volatile fatty acid concentrations were reduced below 200 mg chemical oxygen demand/L (187 mg/L as acetic acid). Enhancement of sludge digestion was observed in those reactors where codigestion of sludge and FOG took place, which was attributed to a higher level of microbial activity maintained in these reactors as a result of FOG degradation. The results of this study demonstrate that beneficial use of FOG through codigestion with municipal sludge is feasible.     

Color and COD removal from wastewater containing Reactive Black 5 using Fenton's oxidation process

In this study, Reactive Black 5 (RB5) was removed from synthetic wastewater using Fenton's oxidation (FO) process. Experiments were conducted on the samples containing 100 and 200 mg l(-1) of RB5 to remove the dye toxicity. Seventy-five milligram per litre of RB5 caused 25% toxicity on 24-h born daphnids whereas 100 mg l(-1) of RB5 displayed 100% toxicity on Daphnia magna. The study was performed in a systematic approach searching optimum values of FeSO(4) and H(2)O(2) concentrations, pH and temperature. Optimum pH and temperature for 100 mg l(-1) of RB5 were observed as 3.0 and 40 degrees C, respectively, using 100 mg l(-1) of FeSO(4) and 400 mg l(-1) of H(2)O(2) resulted in 71% chemical oxygen demand (COD) and 99% color removal. For 200 mg l(-1) of RB5, 84% COD removal was obtained using 225 mg l(-1) of FeSO(4) and 1000 mg l(-1) of H(2)O(2) yielding 0.05 molar ratio at pH 3.0 and 40 degrees C. Color removal was also more than 99%. The optimum conditions determined in accordance with the literature data. The H(2)O(2) requirement seems to be related to initial COD of the sample. FeSO(4)/H(2)O(2) ratios found were not changed for both concentrations. The temperature affected the COD removal significantly at high degrees. Toxicity was completely removed for each concentration of RB5 at optimum removal conditions.     

Climate change effects on aquatic biota, ecosystem structure and function

Climate change is projected to cause significant alterations to aquatic biogeochemical processes, (including carbon dynamics), aquatic food web structure, dynamics and biodiversity, primary and secondary production; and, affect the range, distribution and habitat quality/quantity of aquatic mammals and waterfowl. Projected enhanced permafrost thawing is very likely to increase nutrient, sediment, and carbon loadings to aquatic systems, resulting in both positive and negative effects on freshwater chemistry. Nutrient and carbon enrichment will enhance nutrient cycling and productivity, and alter the generation and consumption of carbon-based trace gases. Consequently, the status of aquatic ecosystems as carbon sinks or sources is very likely to change. Climate change will also very likely affect the biodiversity of freshwater ecosystems across most of the Arctic. The magnitude, extent, and duration of the impacts and responses will be system- and location-dependent. Projected effects on aquatic mammals and waterfowl include altered migration routes and timing; a possible increase in the incidence of mortality and decreased growth and productivity from disease and/or parasites; and, probable changes in habitat suitability and timing of availability.     

Prediction of environmental partition coefficients and the Henry's law constants for 135 congeners of chlorodibenzothiophene

Polychlorinated dibenzothiophenes (PCDTs) could be classified as persistent organic pollutants (POPs) in the environment and are particularly interesting due to their structural resemblance to highly toxic dioxins. We show here some basic environmental properties such as n-octanol water (K_OW), n-octanol/air (K_OA) and air/water (K_AW) partition coefficients as well as Henry’s law constants (K_H) for all 135 congeners of chlorodibenzothiophene. Predictions were made by regression of principal components (PCR) and with aid of a set of standard chemicals, for which physical–chemical properties are well featured. Computed K_OW, K_OA, K_AW and K_H values for mono-CDTs ranged, respectively, between 4.66 and 4.71, 7.48 and 7.55, −2.84 and −2.82, 3.56 and 3.74; for di-CDTs between 5.02 and 5.28, 8.03 and 8.29, −3.01 and −2.95, 2.42 and 2.75; for tri-CDTs between 5.53 and 5.70, 8.65 and 8.87, −3.2 and −3.11, 1.58 and 1.92; for tetra-CDTs between 5.95 and 6.13, 9.27 and 9.50, −3.39 and −3.27, 1.02 and 1.33; for penta-CDTs between 6.38 and 6.51, 9.88 and 10.05, −3.54 and −3.45, 0.72 and 0.88; for hexa-CDTs between 6.83 and 6.97, 10.54 and 10.66, −3.72 and −3.64, 0.47 and 0.56; for hepta-CDTs between 7.28 and 7.35, 11.12 and 11.20, −3.81 and −3.87, 0.33 and 0.38; for octa-CDT 7.74, 11.78, −4.04 and 0.23. An estimated value of the three types of partition coefficient and Henry’s law constants suggest that polychlorinated dibenzothiophenes are lipophilic and semi-volatile persistent organic pollutants. Their mobility in the environment seems to be very similar to that of some well-known POPs such as polychlorinated dibenzofurans, -dibenzo-p-dioxins, and -biphenyls or organochlorine pesticides.     

Macro, minor and toxic elemental uptake and distribution in Hypoxis hemerocallidea, "the African Potato"--an edible medicinal plant

The elemental uptake and distribution, in various parts of the admired herbal plant, Hypoxis hemerocallidea, the 'African potato' and its ability to accumulate elements in response to the growth soil quality are investigated. The total and exchangeable concentrations of twelve elements in the growth soils and their distribution in the roots, potato bulb and leaves of the plants grown under four different settings were compared. The typical concentrations of the twelve selected elements, in the bulb and leaves of the plant grown in a nursery pot (site 2) were (in microg g(-1)dry weight) Ca (8430 and 27075), Mg (2113 and 1566), Fe (66 and 150), Al (10 and 368), Zn (105 and 6.1), Mn (42 and 51), Cu (7.2 and 20.8), Ba (0.23 and 4.44), Co (0.20 and 0.42), As (2.05 and 24.56), Hg (0.92 and 1.82) and Cr (0.13 and 0.33). Except for Ca, Mg, Zn and Mn, the exchangeable cation concentrations in all the growth soils were low. Ca, Mg, Mn, Zn and As had bioaccumulation factors >1. Fe, Al and Co concentrations were high in the roots with little in the rest of the plant. High concentration of arsenic (approximately 13 microg g(-1) dry weight) with bioaccumulation factors of 7 and 20 were observed in the roots and leaves of the plant respectively (site 2), but the concentration of mercury in bulb was very low (0.92 microg g(-1) dry weight).     

Natural formation and degradation of chloroacetic acids and volatile organochlorines in forest soil--challenges to understanding

- DOI: http:/dx.doi.org/10.1065/espr2005.06.262 Goal, Scope and Background The anthropogenic environmental emissions of chloroacetic acids and volatile organochlorines have been under scrutiny in recent years because the two compound groups are suspected to contribute to forest dieback and stratospheric ozone destruction, respectively. The two organochlorine groups are linked because the atmospheric photochemical oxidation of some volatile organochlorine compounds is one source of phytotoxic chloroacetic acids in the environment. Moreover, both groups are produced in higher amounts by natural chlorination of organic matter, e.g. by soil microorganisms, marine macroalgae and salt lake bacteria, and show similar metabolism pathways. Elucidating the origin and fate of these organohalogens is necessary to implement actions to counteract environmental problems caused by these compounds. Main Features While the anthropogenic sources of chloroacetic acids and volatile organochlorines are relatively well-known and within human control, knowledge of relevant natural processes is scarce and fragmented. This article reviews current knowledge on natural formation and degradation processes of chloroacetic acids and volatile organochlorines in forest soils, with particular emphasis on processes in the rhizosphere, and discusses future studies necessary to understand the role of forest soils in the formation and degradation of these compounds. Results and Discussion Reviewing the present knowledge of the natural formation and degradation processes of chloroacetic acids and volatile organochlorines in forest soil has revealed gaps in knowledge regarding the actual mechanisms behind these processes. In particular, there remains insufficient quantification of reliable budgets and rates of formation and degradation of chloroacetic acids and volatile organochlorines in forest soil (both biotic and abiotic processes) to evaluate the strength of forest ecosystems regarding the emission and uptake of chloroacetic acids and volatile organochlorines, both on a regional scale and on a global scale. Conclusion It is concluded that the overall role of forest soil as a source and/or sink for chloroacetic acids and volatile organochlorines is still unclear; the available laboratory and field data reveal only bits of the puzzle. Detailed knowledge of the natural degradation and formation processes in forest soil is important to evaluate the strength of forest ecosystems for the emission and uptake of chloroacetic acids and volatile organochlorines, both on a regional scale and on a global scale. Recommendation and Perspective As the natural formation and degradation processes of chloroacetic acids and volatile organochlorines in forest soil can be influenced by human activities, evaluation of the extent of this influence will help to identify what future actions are needed to reduce human influences and thus prevent further damage to the environment and to human health caused by these compounds.     

Forests under the Southern Cross: The forest environmental frontier in Australia and New Zealand

Australia and New Zealand share many historical and contemporary commonalities. These define five contemporary forest environmental frontiers—for First Nations peoples, between agriculture and forestry, in forest management, in urban and peri-urban environments, and in relation to climate change. In both countries, the First Nations frontier is expanding in scale and significance with those peoples’ rights to land and forests. Frontiers with agriculture and in forest management are longstanding but dynamic and as yet little realised in relation to the need for forest and landscape restoration. Both countries are highly urbanised, elevating the significance of the urban and peri-urban frontier, particularly in the context of climate change. In both countries, forests will be profoundly impacted by climate change and are central to mitigation and adaptation strategies. Experience within and intersections between the frontiers offer encouraging prospects for synergies and for learning between the two countries and more widely.     

Fine PM measurements: personal and indoor air monitoring

This review compiles personal and indoor microenvironment particulate matter (PM) monitoring needs from recently set research objectives, most importantly the NRC published "Research Priorities for Airborne Particulate Matter (1998)". Techniques and equipment used to monitor PM personal exposures and microenvironment concentrations and the constituents of the sampled PM during the last 20 years are then reviewed. Development objectives are set and discussed for personal and microenvironment PM samplers and monitors, for filter materials, and analytical laboratory techniques for equipment calibration, filter weighing and laboratory climate control. The progress is leading towards smaller sample flows, lighter, silent, independent (battery powered) monitors with data logging capacity to store microenvironment or activity relevant sensor data, advanced flow controls and continuous recording of the concentration. The best filters are non-hygroscopic, chemically pure and inert, and physically robust against mechanical wear. Semiautomatic and primary standard equivalent positive displacement flow meters are replacing the less accurate methods in flow calibration, and also personal sampling flow rates should become mass flow controlled (with or without volumetric compensation for pressure and temperature changes). In the weighing laboratory the alternatives are climatic control (set temperature and relative humidity), and mechanically simpler thermostatic heating, air conditioning and dehumidification systems combined with numerical control of temperature, humidity and pressure effects on flow calibration and filter weighing.     

中国城市污水处理厂污泥处理、处置问题探讨分析

明确了有关污泥处理、处置的术语和定义,通过对我国污水处理厂污水处理工艺与污泥处理、处置现状的调查分析,认为污水处理工艺与污泥处理和最终处置方式有关;同时对污水处理厂污泥处理、处置中土地利用问题和处理、处置费用问题进行探讨,并提出了相关建议.     

植物对氮、磷去除效果及克藻效应的研究

于夏季，在实验室和莫愁湖现场，开展了苦草和美人蕉对氮、磷去除效果及克藻效应的研究，结果表明，无论是在现场还是实验室，苦草和美人蕉对总氮、总磷都有明显的去除效果，且随着时间的增加，去除率也随之增大。在实验与现场条件，美人蕉与苦草对总氮和总磷的去除率之间没有显著差异。苦草和美人蕉都对蛋白核小球藻和铜绿微囊藻两种藻类表现出显著的抑制作用，但在实验与现场条件下，美人蕉和苦草对两种藻类的抑制效应存在着显著差异，而对于藻种则二者均表现出一定的选择性抑制作用。     

Policy and Science Implications of the Framing and Qualities of Uncertainty in Risks: Toxic and Beneficial Fish from the Baltic Sea

Policy and research issues in the framing and qualities of uncertainties in risks are analyzed, based on the assessments of dioxin-like compounds (DLCs) and other ingredients in Baltic Sea fish, a high-profile case of governance. Risks are framed broadly, to then focus on dioxins and beneficial fatty acids, fish consumption, human health, and science-management links. Hierarchies of uncertainty (data, model, decision rule, and epistemic) and ambiguity (of values) are used to identify issues of scientific and policy contestation and opportunities for resolving them. The associated complexity of risks is illustrated by risk–benefit analyses of fish consumption and by evaluations of guideline values, highlighting value contents and policy factors in presumably scientific decision criteria, and arguments used in multi-dimensional risk and benefit comparisons. These comparisons pose challenges to narrow assessments centered, for e.g., on toxicants or on food benefits, and to more many-sided and balanced risk communication and management. It is shown that structured and contextualized treatment of uncertainties and ambiguities in a reflexive approach can inform balances between wide and narrow focus, detail and generality, and evidence and precaution.     

Transformation and Ecotoxicity of Carbamic Pesticides in Water (5 pp)

Background N-methylcarbamate insecticides are widely used chemicals for crop protection. This study examines the hydrolytic and photolytic cleavage of benfuracarb, carbosulfan and carbofuran under natural conditions. Their toxicity and that of the corresponding main degradation products toward aquatic organisms were evaluated. Methods Suspensions of benfuracarb, carbosulfan and carbofuran in water were exposed to sunlight, with one set of dark controls, for 6 days, and analyzed by 1H-NMR and HPLC. Acute toxicity tests were performed on Brachionus calyciflorus, Daphnia magna, and Thamnocefalus platyurus. Chronic tests were performed on Pseudokirchneriella subcapitata, and Ceriodaphnia dubia. Results and Discussion Under sunlight irradiation, benfuracarb and carbosulfan gave off carbofuran and carbofuran-phenol, while only carbofuran was detected in the dark experiments. The latter was degraded to phenol by exposure to sunlight. Effects of pH, humic acid and KNO3 were evaluated by kinetics on dilute solutions in the dark and by UV irradiation, which evidenced the lability of the pesticide at pH 9. All three pesticides and phenol exhibited acute and higher chronic toxicity towards the aquatic organisms tested. Conclusion Investigation on the hydrolysis and photolysis of benfuracarb and carbosulfan under natural conditions provides evidence concerning the selective decay to carbofuran and/or phenol. Carbofuran is found to be more persistent and toxic. Recommendations and Outlook The decay of benfuracarb and carbosulfan to carbofuran and the relative stability of this latter pesticide account for many papers that report the detection of carbofuran in water, fruits and vegetables.