Etude sur l'activite initiale et la persistance d'un larvicide experimental a base de bacillus thuringiensis var. israelensis et d'une preparation commerciale contenant l'insecticide organophosphore temephos

Abstract

The larvicide activity of the experimental preparation SAN 402 I WDC containing B. Thuringiensis var. Israelensis and that of Abate 500 E (44 % temephos) were tested on the larvae of Aedes aegypti. The studies were performed on the following media : distilled water, pure and buffered at pH 9, 7 and 4 and pond water whether or not free from materials in suspension. The activity of both preparations is not influenced by the composition of the media, exception made for the presence of materials in suspension. The persistance varies according to the kind of the media and the concentration level. It is in general rather low. Both preparations behave rather similar, the microbial insecticide however is more influenced by the presence of materials in. suspension.     

Bactericidal activity of Cu-, Zn-, and Ag-containing zeolites toward <Emphasis Type="Italic">Escherichia coli</Emphasis> isolates

Two types of zeolites—natural clinoptilolite (NZ) and synthetic zeolite A (A)—were enriched with approx. 0.25 mmol of Cu(II), Zn(II), or Ag(I) ions, and the obtained materials (M-Z) were tested against three different isolates of Escherichia coli. Two isolates were environmental isolates from waters in Serbia whereas the third one was DSM 498. Antibacterial activity was studied in different water media—nutrient-rich media (peptone water), water from Sava Lake, and commercially available spring water. The Ag-containing zeolites showed bactericidal activity in the nutrient-rich peptone water after 1 h of contact. Cu- and Zn-containing zeolites showed bactericidal activity in real water samples. Antibacterial activity of the M-Z decreases in all three examined water media in the following order: Ag-NZ ≈ Ag-A > Cu-NZ ≈ Cu-A > Zn-NZ >>> Zn-A, suggesting that mainly the metal type and not the zeolite type have a role in the antibacterial activity. Leaching experiments showed small amounts of the leached Cu(II) and Zn(II) ions, indicating that the antibacterial activity is not due to the metal ions but should be attributed to the M-Z itself. However, leached amounts of Ag(I) from Ag-NZ and Ag-A in peptone water indicate that the released Ag(I) could be mainly responsible for the bactericidal effect of the Ag(I)-containing zeolites. Since no loss of cellular material was found, the antibacterial activity is not attributed to cytoplasmic membrane damage.     

Volatilization of contaminants from suspended sediment in a water column during dredging

Remedial dredging of contaminated bed sediments in rivers and lakes results in the suspension of sediment solids in the water column, which can potentially be a source for evaporation of hydrophobic organic compounds (HOCs) associated with the sediment solids. Laboratory experiments were conducted in an oscillating grid chamber to simulate the suspension of contaminated sediments and flux to air from the surface of the water column. A contaminated field sediment from Indiana Harbor Canal (IHC) and a laboratory-inoculated University Lake (UL) sediment, Baton Rouge, LA, were used in the experiments, where water and solids concentration and particle size distribution were measured in addition to contaminant fluxes to air. A transient model that takes into account contaminant desorption from sediment to water and evaporation from the water column was used to simulate water and sediment concentrations and air fluxes from the solids suspension. In experiments with both sediments, the total suspended solids (TSS) concentration and the average particle diameter of the suspended solids decreased with time. As expected, the evaporative losses were higher for compounds with higher vapor pressure and lower hydrophobicity. For the laboratory-inoculated sediment (UL), the water concentrations and air fluxes were high initially and decreased steadily implying that contaminant release to the water column from the suspended solids was rapid, followed by evaporative decay. For the field sediments (IHC), the fluxes and water concentrations increased initially and subsequently decreased steadily. This implied that the initial desorption to water was slow and that perhaps the presence of oil and grease and aging influenced the contaminant release. Comparison of the model and experimental data suggested that a realistic determination of the TSS concentration that can be input into the model was the most critical parameter for predicting air emission rates.     

Role of biological activity and biomass distribution in air biofilter performance

The effects of temporal and spatial changes in biological activity and biomass amount on biofilter performance were investigated in a lab-scale trickle-bed air biofilter at a toluene loading of 46.9gm(-3)h(-1) under two different experimental strategies, namely, periodic backwashing at a rate of 1h once a week and 2d starvation. Analysis of the overall reaction for toluene metabolism revealed that cell synthesis was relatively favored over toluene oxidation in the inlet section of the biofilter, but over time its oxidation became favored throughout the biofilter bed. Periodic in situ backwashing with media fluidization effectively made even spatial distribution of biomass along the bed media, by which consistent high removal performance in the biofilter has been attained. After 2d starvation, the ratio of the biofilm EPS to the total biomass increased along the media bed depth, while the total biomass in the media bed subsequently decreased. The presence of sufficient biomass and microbial activity favorably influenced biofilter reacclimation after restart-up following starvation.     

Removal possibilities of colloidal chromium (III) oxide from water using polyacrylic acid

The lack of water is the most serious threat to humanity that leads to more efficient water and sewage treatment. Currently, many scientists are looking for new coagulants, flocculants and physicochemical methods allowing for sufficient removal of pollutants from water. The presence of various types of pigments, including chromium (III) oxide, poses the major problem. Even small amounts of these substances inhibit life processes in water. In this paper, the stability of Cr₂O₃ suspension in the absence and the presence of polyacrylic acid (PAA) was determined. To explain the changes in the system stability, the adsorption and electrokinetic measurements were performed. The chromium (III) oxide suspension not containing PAA is the most stable at pH?=?3. Under these conditions, each positively charged solid particle is surrounded by a negatively charged diffusion layer which protects from particle collision and aggregates formation (electrostatic stabilization). In turn, the Cr₂O₃ suspension containing the PAA is most unstable also at pH?=?3. In this case, the polymer causes destabilization of the colloidal suspension, which results from charge neutralization of solid particles by adsorbed PAA.     

Enhanced stability and dechlorination activity of pre-synthesis stabilized nanoscale FePd particles

Nanoscale zero-valent iron (NZVI) particles are promising materials for the in-situ remediation of a wide variety of source zone contaminants. This study presents the results of a systematic investigation of the stability of bimetallic FePd nanoparticle suspensions in water and their capability to degrade trichloroethylene (TCE) synthesized in the presence of various stabilizers (i.e., carboxymethyl cellulose (CMC), polyvinylpyrrolidone (PVP), and guar gum). Results indicate a dramatic improvement in FePd suspension stability when the stabilizer is present in the matrix during the nanoparticle synthesis step. Stability enhancement is controlled by iron nanoparticle/stabilizer electrostatic and steric interactions, which are a function of the molecular structure of the stabilizer. Stabilization mechanisms differed for each stabilizer with CMC and guar gum exhibiting the best nanoparticle suspension stability improvement. Results suggest that the complexation of iron precursors with the stabilizer, during synthesis, plays a key role in nZVI stability improvement. In case of guar gum, gelation during synthesis significantly increased suspension viscosity, enhancing suspension stability. The capability of these materials to degrade TCE was also investigated. Results demonstrated that when stabilizers were present in the matrix dechlorination rates increased significantly. FePd nanoparticles in CMC had the highest observed rate constant; however the highest surface area-normalized rate constant was obtained from FePd stabilized in PVP360K. Results from this study can be used to aid in the selection of appropriate iron nanoparticle stabilizers. Stabilizer selection should be assessed on a case by case basis as no stabilizer will meet the needs of all in-situ remediation applications.     

New Fe-immobilized natural bentonite plate used as photo-Fenton catalyst for organic pollutant degradation

Novel photo-Fenton catalysts were prepared by immobilizing iron species on commercial bentonite plates via two methods: (1) ion exchange reaction (Fe³⁺ vs. Na⁺) by aqueous suspension powder-clay/FeCl₃ followed by plate preparation, and (2) forced hydrolysis of Fe(NO₃)₃ onto a prefabricated clay plate. The last method led to a more photo-active Fe-oxide/bentonite plate. This material allowed, at a non-adjusted initial pH of 5.5 and in the presence of H₂O₂, the total degradation of resorcinol and 55% mineralization in 80 and 100 min of irradiation, respectively. The reached degradation percentages were correlated to the presence of dissolved iron, demonstrating that in these processes, the homogeneous photo-Fenton reactions were mainly responsible for the resorcinol elimination.Likewise, in slurry system, where clay has normally an increased surface area, there was no increase in activity because of a reduced leached iron probably due to the diminished light penetration in the suspension. Despite the lower surface area, in comparison to that of the slurry, the clay plates have the advantage, as heterogeneous photo-catalysts, that separation of the reaction media after treatment is not needed, and thus, a potential use for batch and continuous reaction systems is proposed.     

Evaluating three trace metal contaminated sites: a field and laboratory investigation

Selecting guidelines to evaluate elevated metals in urban brownfields is hindered by the lack of information for these sites on ecosystem structure and function. A study was performed to compare three trace metal-contaminated sites in the metropolitan Montreal area. The goal was to obtain an idea of the organisms that may be present on urban brownfields and to measure if elevated metals alter the presence and activity of the indigenous biota. Field and laboratory studies were conducted using simple methodologies to determine the extent to which microbial activity affected by trace metal content, to assess diversity of plant and soil invertebrate communities and to measure phytoaccumulation of trace metals. It was found that microbial activity, as measured by substrate-induced respiration (SIR) and nitrification, was not affected by the levels of soil Cd, Cu, Ni, Pb and Zn recorded on the sites. Seven of the 12 invertebrate groups collected were sampled on soils with similar Cd, Cu, Ni, Pb and Zn concentrations. Diversity of plant species increased as a function of the length of time the sites had been inactive. Levels of metals in plant tissue were influenced by soil characteristics and not by total soil Cd, Cu, Ni, Pb and Zn.     

Impact of river overflowing on trace element contamination of volcanic soils in south Italy: part II. Soil biological and biochemical properties in relation to trace element speciation

The effect of heavy metal contamination on biological and biochemical properties of Italian volcanic soils was evaluated in a multidisciplinary study, involving pedoenvironmental, micromorphological, physical, chemical, biological and biochemical analyses. Soils affected by recurring river overflowing, with Cr(III)-contaminated water and sediments, and a non-flooded control soil were analysed for microbial biomass, total and active fungal mycelium, enzyme activities (i.e., FDA hydrolase, dehydrogenase, beta-glucosidase, urease, arylsulphatase, acid phosphatase) and bacterial diversity (DGGE characterisation). Biological and biochemical data were related with both total and selected fractions of Cr and Cu (the latter deriving from agricultural chemical products) as well as with total and extractable organic C. The growth and activity of soil microbial community were influenced by soil organic C content rather than Cu or Cr contents. In fact, positive correlations between all studied parameters and organic C content were found. On the contrary, negative correlations were observed only between total fungal mycelium, dehydrogenase, arylsulphatase and acid phosphatase activities and only one Cr fraction (the soluble, exchangeable and carbonate bound). However, total Cr content negatively affected the eubacterial diversity but it did not determine changes in soil activity, probably because of the redundancy of functions within species of soil microbial community. On the other hand, expressing biological and biochemical parameters per unit of total organic C, Cu pollution negatively influenced microbial biomass, fungal mycelium and several enzyme activities, confirming soil organic matter is able to mask the negative effects of Cu on microbial community.     

Occurrence and source of brominated organic compounds in surface waters

Monitoring of organic halogen compounds, measured as adsorbable organically bound bromine (AOBr), in an eutrophic lake, which is influenced by treated waste water, revealed repeatedly high concentrations of organobromine compounds in late summer, whereas five times lower values were measured during the rest of the year. It was possible to reproduce the in situ observed AOBr increase in the laboratory. Batch experiments were performed with lake water from two different lakes and an algae culture. It could be shown that the AOBr production is not limited to strong waste water influenced lakes. Furthermore, the AOBr formation requires light and the presence of algae, and thus is most probably biotic in nature. A low content of nutrients favours the formation of organic bromine compounds. To our knowledge this is the first report about the seasonally occurrence of naturally produced organic bromine compounds in lakes/surface waters.     

物料下落过程中可吸入颗粒物产生特性及控制技术

利用实验室新设计开发的一套装置,研究物料自由下落过程影响可吸入颗粒物产生的因素.通过实验分别测定不同物料、质量流量、含水量、粒径组成和下垫面5个因素对可吸入颗粒物产生的影响.实验结果表明,不同物料可吸入颗粒物产生率不同;随着质量流量和物料含水量的增加,可吸入颗粒物产生率减小,加水是减少可吸入颗粒物排放的最有效方法之一;不同粒径组成和不同下垫面对可吸入颗粒物产生也有影响,但作用并不显著.     

The influence of environmental factors on the molluscicidal activity of Euphorbia milii latex.

The present study was undertaken to investigate the influence of biotic (snail size and presence of food during the test) and abiotic factors (temperature, water hardness and concentration of organic materials) on the molluscicidal activity of Euphorbia milii latex. Bioassays were conducted with B. glabrata (10 snails per concentration) and snail lethality was evaluated after 24 hr and 48 hr of exposure to lyophilized latex solutions. Neither the degree of water hardness, nor the presence of food during the test affected latex-induced snail mortality. The snail size had a minor influence on E. milii-induced snail lethality. Newly-hatched (shell diameter < or = 1 mm) as well as young (3-8 mm) snails were slightly less susceptible than older (10-25 mm) mollusks. On the other hand, the molluscicidal effect of E. milii latex was modified by environmental factors such as temperature (i.e., LC50 and LC90 values were halved for every 10 degrees C rise in temperature) and concentration of organic materials in the water (i.e. the higher the concentration of organic matter, the higher the LC50 value). The efficacy of E. milii latex as a molluscicide can be modified by factors such as water temperature and concentration of organic materials, and to a lesser extent by snail size.     

Assessment of organochlorine pesticide residues in Atlantic Rain Forest fragments, Rio de Janeiro, Brazil

A superficial water quality survey in a watershed of the Paraíba do Sul River, the main water supply for the most populated cities of southeastern Brazil, was held in order to assess the impact of the expansion of agricultural activity in the near border of the Atlantic Rain Forest. The aim of this study was to investigate the presence of priority organochlorine pollutants in soils and superficial waters of Atlantic rainforest fragments in Teresópolis, Rio de Janeiro State. Soil sample preparations were compared by using ultrasound, microwave assisted extraction and Soxhlet extraction. Recoveries of matrix spiked samples ranged from 70 to 130%. Analysis of a certified soil material showed recoveries ranging from 71 to 234%. Although low concentrations of organochlorine residues were found in water and soil samples, this area is of environmental importance and concern, thus demanding a monitoring program of its compartments.     

Metabolic enzymes activity and histomorphology in the liver of whitefish (Coregonus lavaretus L.) and pike (Esox lucius L.) inhabiting a mineral contaminated lake

The effects of wastewater from a mining and ore-dressing mill on fish in Lake Kostomukshskoe, which is used as a cesspool of circulating water and for storage of industrial wastes produced by the Kostomuksha mining and ore-dressing mill in northwest Russia, were studied. The lake is characterized by heavy mineralization, high pH, elevated levels of K⁺, Li⁺, SO₄ ^2?, NO^2?, Cl^?, Li, Mn, and Ni, and the presence of a fine-dispersed mechanical suspension. To assess the impact of contamination on fish and determine the mechanisms of their adaptation, we investigated the biochemical indices and histology of the liver of whitefish (Coregonus lavaretus L.) and pike (Esox lucius L.) inhabiting Lake Kostomukshskoe, downstream Lake Koyvas (64° 47′ 30° 59′), and Lake Kamennoe, which is located in a nature preserve and has not been affected by anthropogenic activity (64° 28′ 30° 13′). Changes were detected in the activity of metabolic enzymes (cytochrome c oxidase (COX), lactate dehydrogenase, and glucose-6-phosphate dehydrogenase) in the liver. Specifically, the COX activity in the liver of both fish species from the contaminated lake decreased, indicating a low level of aerobic metabolism. Lipid infiltration was the most visible and widespread change observed in the liver of both fish species; therefore, it can be considered a marker of such long-term contamination. Lesions in pike liver demonstrated a wider range of severity than in those of whitefish. In summary, metabolic enzyme activity and histomorphology of the liver of whitefish and pike differed among lakes in a species-specific manner. The changes in enzyme activity and histomorphological alterations in fish that were observed can be applied for evaluation of freshwater systems that may be subjected to mineral pollution.     

Biodegradation kinetics and toxicity of vegetable oil triacylglycerols under aerobic conditions

The aerobic biodegradation of five triacylglycerols (TAGs), three liquids [triolein (OOO), trilinolein (LLL), and trilinolenin (LnLnLn)] and two solids [tripalmitin (PPP) and tristearin (SSS)] was studied in water. Respirometry tests were designed and conducted to determine the biochemical oxygen demand (BOD) parameters of the compounds. In the case of the solid lipids, the degradation process was limited by their extremely non-polar nature. When added to water, PPP and SSS formed irregular clumps or gumballs, not a fine and uniform suspension required for the lipase activity. After 30 days, appreciable mineralization was not achieved; therefore, first-order biodegradation coefficients could not be determined. The bioavailability of the liquid TAGs was restricted due to the presence of double bonds in the fatty acids (FAs). An autoxidation process occurred in the allylic chains, resulting in the production of hydroperoxides. These compounds polymerized and became non-biodegradable. Nevertheless, the non-oxidized fractions were readily mineralized, and BOD rate constants were estimated by non-linear regression: LLL (k = 0.0061 h⁻¹) and LnLnLn (k = 0.0071 h⁻¹) were degraded more rapidly than OOO (k = 0.0025 h⁻¹). Lipids strongly partitioned to the biomass and, therefore, Microtox^® toxicity was not observed in the water column. However, EC₅₀ values (<15% sample volume) were measured in the solid phase.     

滤布滤池强化处理城市二级出水中试研究

采用滤布滤池对南方某城市污水处理厂二级出水进行强化处理中试研究,以达到中水回用的目的。实验选用氯化铁(FeCl₃)、聚合氯化铝铁（PAFC）和聚合氯化铝（PAC）作为强化滤布滤池除磷效果的混凝剂。当不投加混凝剂时,滤布滤池对TP和COD的平均去除率为28.76%和8%,其中TP的去除效果受进水水质影响较大;当投加氯化铁、聚合氯化铝铁与聚合氯化铝强化滤布滤池时,滤布滤池对TP的平均去除率分别为63.58%、60.13%和66.94%,TP去除效果受进水水质影响较小;对SS的平均去除率分别为70.7%、64.3%和49.1%;对COD平均去除率分别为17.7%、26.3%和27.7%。滤布滤池对TN和NH₃-N去除效果不稳定。     

Perfluoroalkyl and polyfluoroalkyl substances (PFASs) in consumer products in Norway - a pilot study

Perfluoroalkyl and polyfluoroalkyl substances (PFAS) are used in numerous industrial and consumer products because of their special chemical properties, for instance the ability to repel both water and oil. A broad variety of PFAS have been introduced into the Norwegian market through industrial use (e.g. via fire fighting foams and paints) as well as in treated customer products such as textiles and coated paper. Our present knowledge of the exact chemical PFAS compositions in preparations using perfluorinated compounds is limited. This lack of knowledge means that it is difficult to provide an accurate assessment of human exposure to these compounds or to the amount of waste that may contain treated products. It is a growing concern that these potentially harmful compounds can now be found throughout the global environment.Samples of consumer products and preparations were collected in Norway, with supplemental samples from Sweden. In 27 of the 30 analyzed consumer products and preparations a number of polyfluorinated substances that were analyzed were detected but this does not exclude the occurrence of unknown PFAS. Notable was that perfluorooctanesulphonate (PFOS), which has been strictly regulated in Norway since 2007, was found in amounts close to or exceeding the EU regulatory level in 4 of the 30 analyzed products, all within the leather or carpet product groups. High amounts of fluorotelomer alcohols (FTOHs) were found in waterproofing agents, carpets and textiles, consistent with earlier findings by Fiedler et al. (2010). The presence of PFAS in a broad range of consumer products can give rise to a constant diffuse human exposure that might eventually result in harm to humans.     

Chemically catalyzed uptake of 2,4,6-trinitrotoluene by Vetiveria zizanioides

The efficiency of vetiver grass (Vetiveria zizanioides) in removing 2,4,6-trinitrotoluene (TNT) from aqueous media was explored in the presence of a common agrochemical, urea, used as a chaotropic agent. Chaotropic agents disrupt water structure, increasing solubilization of hydrophobic compounds (TNT), thus, enhancing plant TNT uptake. The primary objectives of this study were to: (i) characterize TNT absorption by vetiver in hydroponic media, and (ii) determine the effect of urea on chemically catalyzing TNT uptake by vetiver grass in hydroponic media. Results showed that vetiver exhibited a high TNT uptake capacity (1.026 mgg(-1)), but kinetics were slow. Uptake was considerably enhanced in the presence of urea, which significantly (p<0.001) increased the 2nd-order reaction rate constant over that of the untreated (no urea) control. Three major TNT metabolites were detected in the roots, but not in the shoot, namely 1,3,5-trinitrobenzene, 4-amino 2,6-dinitrotoluene, and 2-amino 4,6-dinitrotoluene, indicating TNT degradation by vetiver grass.     

Current status and future needs for biological and environmental reference materials certified for methylmercury compounds.

A good quality control/quality assurance programme should be implemented in all environmental or health related studies on mercury and its organic compounds, particularly, for monomethylmercury (MeHg) which is the most toxic mercury compound. This can be achieved initially by analysing suitable certified reference materials (CRMs), which are available from various producers such as the National Institute of Standards and Technology (NIST) from USA, National Institute of Environmental Studies (NIES), National Research Council of Canada (NRCC), Standards, Measurements and Testing programme (SM&T) of the European Commission, and the International Atomic Energy Agency (IAEA). It is well understood that these materials are not covering present needs, as most of them are of the marine origin, while many laboratories are conducting research and monitoring in terrestrial ecosystems and fresh water environment. In addition, CRMs for human exposure assessment, such as blood, urine, and hair at several levels of concentrations are still lacking. Therefore, many other actions should be undertaken to achieve, improve and/or maintain quality of data, including participation in interlaboratory studies, proficiency testing and production of laboratory reference materials. A review of these actions has shown that MeHg compounds determination in samples such as soil, sediment and water is rather difficult and the results are also method dependent. In addition, it has been shown that some of the most frequently employed analytical methods may be a subject to spurious MeHg formation in the presence of high concentrations of inorganic mercury and organic matter. These findings have put a number of previous data on MeHg in question and consequently prompt actions were undertaken by a number of well experienced laboratories and producers of CRMs. So far, it is shown that the results obtained by various laboratories using different analytical techniques agree well with certified values in all RMs certified for MeHg. This suggests that comparability of data can be achieved, which however is not a guarantee of the true values.     

Preparation and characterization of polycaprolactone nanocapsules containing pretilachlor as a herbicide nanocarrier

Polycaprolactone nanocapsules (PCL) containing pretilachlor were prepared, and Fourier transform infrared spectroscopy, atomic force microscopy, and transmission electron microscopy were used for their structural and morphological investigations. The results revealed that the nanocapsules had irregular shape and their particles size was in the range of 70–200 nm. The encapsulation efficiency of pretilachlor was measured as 99.5 ± 1.3% using high-performance liquid chromatography analysis. The physicochemical stability studies over 60 days showed that the nanocapsules were stable in the suspension without any aggregation. The herbicide activity was examined in a pre-emergence manner using barnyard grass as a target plant and rice as a non-target plant. The nanoformulation had no negative effect on rice plant. However, its effect on barnyard grass was significant. The cytotoxicity analysis indicated that the nanocapsulated herbicide is less toxic rather than the commercial formulation. Therefore, encapsulation of pretilachlor in PCL nanocapsules can be used effectively to construct environmentally friendly PCL-herbicide systems in agriculture.