Estimation of ecotoxicity of petroleum hydrocarbon mixtures in soil based on HPLC–GCXGC analysis

Detailed HPLC–GCXGC/FID (high performance liquid chromatography followed by comprehensive two-dimensional gas chromatography with flame-ionization detection) analysis of oil-contaminated soils was performed to interpret results of selected acute ecotoxicity assays. For the five ecotoxicity assays tested, plant seed germination and Microtox^® were selected as most sensitive for evaluating ecotoxicity of the oil in the soil phase and in the leaching water, respectively. The measured toxicity for cress when testing the soil samples did not correspond to TPH concentration in the soil. A detailed chemical composition analysis of the oil contamination using HPLC–GCXGC/FID allows to better predict the ecotoxicological risk and leaching potential of petroleum hydrocarbons in soil. Cress biomass production per plant was well correlated to the total aromatic hydrocarbon concentration (R² = 0.79, n = 6), while cress seed germination was correlated (R² = 0.82, n = 6) with total concentration of “highly water-soluble aromatic hydrocarbons” (HSaromatics). The observed ecotoxicity of the leaching water for Microtox-bacteria related well to calculated (based on the HPLC–GCXGC/FID results) petroleum hydrocarbon equilibrium concentrations in water.     

Bioaccumulation Factors (BAFs) and Biota to Sediment Accumulation Factors (BSAFs) for PCBs in pike and eels

“Freely-dissolved” aqueous concentrations of 9 trichlorothrough heptachlorobiphenyls are reported, alongside those in sediments and fish from the R. Severn. For most congeners, BSAFs and lipid-normalised BAFs for pike exceed those for eels. Whilst R. Severn BSAFs are comparable with those for L. Ontario trout and New Bedford Harbour flounder, R. Severn BAFs are 1–2 orders of magnitude lower. This discrepancy may be due to inter-species variability, as well as inter-laboratory differences between operational definitions of “freely-dissolved” aqueous PCB, underlining that the same operational definition must be employed if R. Severn BAFs are extrapolated elsewhere. For eels, correlation of Log K^ow with Log BAF is better (R² = 0.66) than with BSAF (R² = 0.13), whilst similar correlation coefficients (R² = 0.81 and 0.82) were observed for pike. When Log K^ow is plotted against BSAF and Log BAF for both species combined, better correlation is observed for Log BAF (R² = 0.65), than BSAF (R² = 0.36). For both species combined, the observed relationship between Log BAF and Log K^ow for trichloro-through heptachlorobiphenyls is: Log BAF = 0.96 * Log K^ow −0.24.     

One-electron standard reduction potentials of nitroaromatic and cyclic nitramine explosives

Extensive studies have been conducted in the past decades to predict the environmental abiotic and biotic redox fate of nitroaromatic and nitramine explosives. However, surprisingly little information is available on one-electron standard reduction potentials (E^o(R-NO₂/R-NO₂⁻)). The E^o(R-NO₂/R-NO₂⁻) is an essential thermodynamic parameter for predicting the rate and extent of reductive transformation for energetic residues. In this study, experimental (linear free energy relationships) and theoretical (ab initio calculation) approaches were employed to determine E^o(R-NO₂/R-NO₂⁻) for nitroaromatic, (caged) cyclic nitramine, and nitroimino explosives that are found in military installations or are emerging contaminants. The results indicate a close agreement between experimental and theoretical E^o(R-NO₂/R-NO₂⁻) and suggest a key trend: E^o(R-NO₂/R-NO₂⁻) value decreases from di- and tri-nitroaromatic (e.g., 2,4-dinitroanisole) to nitramine (e.g., RDX) to nitroimino compound (e.g., nitroguanidine). The observed trend in E^o(R-NO₂/R-NO₂⁻) agrees with reported rate trends for reductive degradation, suggesting a thermodynamic control on the reduction rate under anoxic/suboxic conditions.     

Influence of meteorological factors and polluting environment on rain chemistry and wet deposition in a rural area near Chimay,Belgium

This paper focuses on a detailed analysis of the effects of meteorological factors explaining the variability of rain composition.Inorganic composition of 113 individual rain events was measured from May 2002 to October 2005 at a rural site near Chimay, in the western part of the Belgian Ardennes. Original models were fitted for each studied ion (H⁺, Mg²⁺, Ca²⁺, K⁺, NH₄⁺, Na⁺, Cl⁻, NO₃⁻ and SO₄²⁻) to relate rain event concentration or wet deposition to the rainfall volume (R), the length of the antecedent dry period (ADP), the volume of the previous event (R_prev) as well as to the mean wind speed and the prevailing wind direction during both the dry and the rainy periods. These variables explained from 32% (H⁺) to 69% (NO₃⁻) of rain concentration variability. Concentrations decreased logarithmically with increasing R values except in case of H⁺ for which a positive effect of rain volume on rain concentration was observed. ADP affected positively rain concentrations of all ions excluding K⁺ and H⁺ for which, respectively, a nonsignificant and a negative effect of this variable was observed. Increasing R_prev strengthened the effect of the variable R on H⁺, Mg²⁺, Ca²⁺, Na⁺, NH₄⁺ and SO₄²⁻ concentrations while it softened the effect of ADP on NO₃⁻ concentrations. Wind speed and direction during dry and rainy periods explained together from 8% (K⁺) to 38% (Na⁺) of rain concentration total variability. R² coefficients of the wet deposition models ranged from 0.51 (K⁺) to 0.79 (SO₄²⁻). For all ions, wet deposition increased significantly with increasing R values while the effects of the other variables were similar to those on concentrations. Wind conditions during dry and rainy periods explained from 4% (H⁺) to 24% (Na⁺) of wet deposition total variability. On an annual scale, the total dry period duration, the total rainfall volume as well as the shape of the distributions of the length of the antecedent dry periods and of the rain event volume are important parameters that influence annual wet deposition.     

Approximation and spatial regionalization of rainfall erosivity based on sparse data in a mountainous catchment of the Yangtze River in Central China

In densely populated countries like China, clean water is one of the most challenging issues of prospective politics and environmental planning. Water pollution and eutrophication by excessive input of nitrogen and phosphorous from nonpoint sources is mostly linked to soil erosion from agricultural land. In order to prevent such water pollution by diffuse matter fluxes, knowledge about the extent of soil loss and the spatial distribution of hot spots of soil erosion is essential. In remote areas such as the mountainous regions of the upper and middle reaches of the Yangtze River, rainfall data are scarce. Since rainfall erosivity is one of the key factors in soil erosion modeling, e.g., expressed as R factor in the Revised Universal Soil Loss Equation model, a methodology is needed to spatially determine rainfall erosivity. Our study aims at the approximation and spatial regionalization of rainfall erosivity from sparse data in the large (3,200 km²) and strongly mountainous catchment of the Xiangxi River, a first order tributary to the Yangtze River close to the Three Gorges Dam. As data on rainfall were only obtainable in daily records for one climate station in the central part of the catchment and five stations in its surrounding area, we approximated rainfall erosivity as R factors using regression analysis combined with elevation bands derived from a digital elevation model. The mean annual R factor (R _a) amounts for approximately 5,222 MJ?mm?ha^?1?h^?1?a^?1. With increasing altitudes, R _a rises up to maximum 7,547 MJ?mm ha^?1?h^?1 a^?1 at an altitude of 3,078 m a.s.l. At the outlet of the Xiangxi catchment erosivity is at minimum with approximate R _a?=?1,986 MJ?mm?ha^?1?h^?1?a^?1. The comparison of our results with R factors from high-resolution measurements at comparable study sites close to the Xiangxi catchment shows good consistance and allows us to calculate grid-based R _a as input for a spatially high-resolution and area-specific assessment of soil erosion risk.     

不同污泥源条件下ANAMMOX启动及其与反硝化协同脱氮对比

采用城市生活污水配水同时启动两组ASBR,R1接种好氧硝化污泥,R2按2∶1混合接种短程硝化和厌氧氨氧化污泥,研究2个ANAMMOX反应器启动的可行性及其差异。实验结果表明,R1和R2均可成功启动ANAMMOX,R1需130 d,R2仅需73 d;稳定期R1和R2反应器NH4+-N、NO2--N和TN去除率分别达95.30%、91.30%、76.28%和96.2%、98.3%、90.1%,且周期内NH4+-N、NO2--N和NO3--N降解规律相似;R1和R2反应器发生的主要反应为厌氧氨氧化,但同时存在反硝化作用;2组反应器稳定运行后污泥颜色、形态及微生物组成相似,经SEM观察多为球状菌。     

An investigation on the physical,chemical and ecotoxicological characteristics of particulate matter emitted from light-duty vehicles

Particulate matter (PM) emitted from three light-duty vehicles was studied in terms of its physicochemical and ecotoxicological character using Microtox^® bioassay tests. A diesel vehicle equipped with an oxidation catalyst emitted PM which consisted of carbon species at over 97%. PM from a diesel vehicle with a particle filter (DPF) consisted of almost equal amounts of carbon species and ions, while a gasoline vehicle emitted PM consisting of ～90% carbon and ～10% ions. Both the DPF and the gasoline vehicles produced a distinct nucleation mode at 120 km/h. The PM emitted from the DPF and the gasoline vehicles was less ecotoxic than that of conventional diesel, but not in direct proportion to the emission levels of the different vehicles. These results indicate that PM emission reductions are not equally translated into ecotoxicity reductions, implying some deficiencies on the actual environmental impact of emission control technologies and regulations.     

Nitrogen and plant population change radiation capture and utilization capacity of sunflower in semi-arid environment

The combination of nitrogen and plant population expresses the spatial distribution of crop plants. The spatial distribution influences canopy structure and development, radiation capture, accumulated intercepted radiation (Sa), radiation use efficiency (RUE), and subsequently dry matter production. We hypothesized that the sunflower crop at higher plant populations and nitrogen (N) rates would achieve early canopy cover, capture more radiant energy, utilize radiation energy more efficiently, and ultimately increase economic yield. To investigate the above hypothesis, we examined the influences of leaf area index (LAI) at different plant populations (83,333, 66,666, and 55,555 plants ha^?1) and N rates (90, 120, and 150 kg ha^?1) on radiation interception (Fi), photosynthetically active radiation (PAR) accumulation (Sa), total dry matter (TDM), achene yield (AY), and RUE of sunflower. The experimental work was conducted during 2012 and 2013 on sandy loam soil in Punjab, Pakistan. The sunflower crop captured more than 96% of incident radiant energy (mean of all treatments), 98% with a higher plant population (83,333 plants ha^?1), and 97% with higher N application (150 kg ha^?1) at the fifth harvest (60 days after sowing) during both study years. The plant population of 83,333 plants ha^?1 with 150 kg N ha^?1 ominously promoted crop, RUE, and finally productivity of sunflower (AY and TDM). Sunflower canopy (LAI) showed a very close and strong association with Fi (R ² = 0.99 in both years), PAR (R ² = 0.74 and 0.79 in 2012 and 2013, respectively), TDM (R ² = 0.97 in 2012 and 0.91 in 2013), AY (R ² = 0.95 in both years), RUE for TDM (RUE_TDM) (R ² = 0.63 and 0.71 in 2012 and 2013, respectively), and RUE for AY (RUE_AY) (R ² = 0.88 and 0.87 in 2012 and 2013, respectively). Similarly, AY (R ² = 0.73 in 2012 and 0.79 in 2013) and TDM (R ² = 0.75 in 2012 and 0.84 in 2013) indicated significant dependence on PAR accumulation of sunflower. High temperature during the flowering stage in 2013 shortened the crop maturity duration, which reduced the LAI, leaf area duration (LAD), crop growth rate (CGR), TDM, AY, Fi, Sa, and RUE of sunflower. Our results clearly revealed that RUE was enhanced as plant population and N application rates were increased and biomass assimilation in semi-arid environments varied with radiation capture capacity of sunflower.     

Kinetics of OH-initiated oxidation of oxygenated organic compounds in the aqueous phase: new rate constants, structure–activity relationships and atmospheric implications

The kinetics of OH oxidation of several organic compounds of atmospheric relevance were measured in the aqueous phase. Relative kinetics were performed using various organic references and OH sources. After validation of the protocol, temperature-dependent rate constants for the reactions of OH radical with ethyl ter-butyl ether (, E_a/R=580 (±560) K), n-butyl acetate ( (±0.4)×10⁹ M⁻¹ s⁻¹, E_a/R=1000 (±200) K), acetone ( (±0.05)×10⁹ M⁻¹ s⁻¹, E_a/R=1400 (±500) K), methyl ethyl ketone (, E_a/R=1200 (±200) K), methyl iso-butyl ketone (, E_a/R=1200 (±300) K) and methylglyoxal (, E_a/R=1100 (±300) K) were determined. A non-Arrhenius behavior was found for phenol, in good agreement with the contribution of an OH addition to the mechanism, which also includes H-abstraction by OH radicals. Global rate constants of acetaldehyde, propionaldehyde, butyraldehyde and valeraldehyde were studied at 298 K only, as these compounds partly hydrate in the aqueous phase. All the obtained data (except those of phenol) complemented by literature data were used to investigate three methods to estimate rate constants for H-abstraction reactions of OH radicals in aqueous solutions when measured data were not available: Evans-Polanyi-type correlations, comparisons with gas-phase data, structure activity relationships (SAR). The results show that the SAR method is promising; however, the data set is currently too small to extend this method to temperatures other than 298 K. The atmospheric impact of aqueous phase OH oxidation of water-soluble organic compounds is discussed with the determination of their global atmospheric lifetimes, taking into account both gas- and aqueous-phase reactivities. The results show that atmospheric droplets can act as powerful photoreactors to eliminate soluble organic compounds from the atmosphere.     

稻壳活性炭制备及其对磷的吸附

利用农业废弃物稻壳经炭化、活化、酸洗、水洗和干燥等工艺制备出一种富含微孔和中孔结构的稻壳活性炭,其BET比表面积达886.3 m2/g。通过正交实验优化了稻壳活性炭对磷吸附条件,并在该条件下进行了吸附等温和吸附动力学实验研究。结果表明,稻壳活性炭对磷的吸附等温曲线能较好符合Langmuir模型(R2=0.9284)和Freundlich模型(R2=0.9208),由Langmuir线性拟合方程可得稻壳活性炭对磷饱和吸附量达6.93 mg/g;稻壳活性炭对磷的吸附过程可用准二级动力学方程描述(R2=0.9968),吸附速度较快,颗粒内扩散为该过程控速阶段。稻壳活性炭作为一种易得、廉价、高效的填料,在农村分散型污水生态处理技术中,具有良好的应用前景。     

Combining Neural Network Models to Predict Spatial Patterns of Airborne Pollutant Accumulation in Soils around an Industrial Point Emission Source

Abstract

Neural networks (NNs) have the ability to model a wide range of complex nonlinearities. A major disadvantage of NNs, however, is their instability, especially under conditions of sparse, noisy, and limited data sets. In this paper, different combining network methods are used to benefit from the existence of local minima and from the instabilities of NNs. A nonlinear k-fold cross-validation method is used to test the performance of the various networks and also to develop and select a set of networks that exhibits a low correlation of errors. The various NN models are applied to estimate the spatial patterns of atmospherically transported and deposited lead (Pb) in soils around an historical industrial air emission point source. It is shown that the resulting ensemble networks consistently give superior predictions compared with the individual networks because, for the ensemble networks, R² values were found to be higher than 0.9 while, for the contributing individual networks, values for R² ranged between 0.35 and 0.85. It is concluded that combining networks can be adopted as an important component in the application of artificial NN techniques in applied air quality studies.     

Effect of deposit age on adsorption and desorption behaviors of ammonia nitrogen on municipal solid waste

Ammonia nitrogen pollution control is an urgent issue of landfill. This research aims to select an optimal refuse for ammonia nitrogen removal in landfill from the point of view of adsorption and desorption behavior. MSW (municipal solid waste) samples which deposit ages were in the range of 5 to 15 years (named as R₁₅, R₁₁, R₇, and R₅) were collected from real landfill site. The ammonia nitrogen adsorption behaviors of MSW including equilibrium time, adsorption isotherms, and desorption behaviors including equilibrium time were determined. Furthermore, the effects of pH, OM, Cu(II), Zn(II), and Pb(II) on adsorption and desorption behavior of ammonia nitrogen were conducted by orthogonal experiment. The equilibrium time of ammonia nitrogen adsorption by each tested MSW was very short, i.e., 20 min, whereas desorption process needed 24 h and the ammonia nitrogen released from refuses was much lesser than that adsorbed, i.e., accounted for 3.20 % (R₁₅), 14.32 % (R₁₁), 20.59 % (R₇), and 20.50 % (R₅) of each adsorption quantity, respectively. The maximum adsorption capacity estimated from Langmuir isotherm appeared in R₁₅-KCl, i.e., 25,000 mg kg^?1. The best condition for ammonia nitrogen removal from leachate was pH >7.5, OM 23.58 %, Cu(II) <5 mg L^?1, Zn(II) <10 mg L^?1, and Pb(II) <1 mg L^?1. Ammonia nitrogen in landfill leachate could be quickly and largely absorbed by MSW but slowly and infrequently released. The refuse deposited for 15 years could be a suitable material for ammonia nitrogen removal.     

Advances in the Analysis of Air Contaminants Comments

Abstract

Methylcyclopentadienyl manganese tricarbonyl (MMT) is an organometallic compound used as an octane improver in unleaded gasoline. The combustion of MMT leads to the formation of manganese (Mn) oxides, mainly Mn₃O₄. The objective of this study is to assess the variations over time and space of respirable (Mn_R) and total (Mn_T) Mn in the urban atmosphere and to evaluate human exposure by inhalation. Two sampling sites were selected on the island of Montreal based on their local traffic density (municipal botanical garden, C^-= 10,000–15,000 vehicles d^-1; Montreal Waterworks, C⁺= 100,000–130,000 vehicles d^-1). Air samplings were made during the day at stations located 10 m from the road using portable pumps, some of which were equipped with a cyclone. Mn_R and Mn_T and other metals were measured on Teflon filters by neutron activation. Mn exposure doses by inhalation were calculated using Monte–Carlo simulations. Mn_R and Mn_T average concentrations were significantly higher at site C⁺ (Mn_R = 0.024 µg m^-3; Mn_T = 0.050 µg m^-3) than at site C^- (Mn_R= 0.015 µg m^-3; Mn_T= 0.027 µg m^-3). Temporal profiles at sites C⁺ and site C^-were similar, with a coefficient of correlation of 0.24 for Mn_R and 0.26 for Mn_T. Trend analyses (ARIMA) also showed that the period of the week (work days vs. off days) was significantly related to Mn_R and Mn_T variations at both sites. The average exposure dose by inhalation to Mn_R and Mn_T ranged from 0.001 to 0.030 µg kg^-1 day^-1 and 0.001 to 0.05 µg kg^-1 day^-1. Mn_R and Mn_T concentrations reflected a positive relationship with traffic density. However, it remains difficult to attribute these results directly to the combustion of MMT in unleaded gasoline. On average, the Mn_R and Mn_T inhalation doses were 2 to 15 times lower than the reference dose (RfC) proposed by the U.S. Environmental Protection Agency (EPA) for the general population.     

Concentration-dependent NH3 deposition processes for mixed moorland semi-natural vegetation

Dry deposition modelling typically assumes that canopy resistance (R_c) is independent of ammonia (NH₃) concentration. An innovative flux chamber system was used to provide accurate continuous measurements of NH₃ deposition to a moorland composed of a mixture of Calluna vulgaris (L.) Hull, Eriophorum vaginatum L. and Sphagnum spp. Ammonia was applied at a wide range of concentrations (1–100 μg m⁻³). The physical and environmental properties and the testing of the chamber are described, as well as results for the moorland vegetation using the ‘canopy resistance’ and ‘canopy compensation point’ interpretations of the data.Results for moorland plant species demonstrate that NH₃ concentration directly affects the rate of NH₃ deposition to the vegetation canopy, with R_c and cuticular resistance (R_w) increasing with increasing NH₃ concentrations. Differences in R_c were found between night and day: during the night R_c increases from 17 s m⁻¹ at 10 μg m⁻³ to 95 s m⁻¹ at 80 μg m⁻³, whereas during the day R_c increases from 17 s m⁻¹ at 10 μg m⁻³ to 48 s m⁻¹ at 80 μg m⁻³. The lower resistance during the day is caused by the stomata being open and available as a deposition route to the plant. R_w increased with increasing NH₃ concentrations and was not significantly different between day and night (at 80 μg m⁻³ NH₃ day R_w=88 s m⁻¹ and night R_w=95 s m⁻¹). The results demonstrate that assessments using fixed R_c will over-estimate NH₃ deposition at high concentrations (over ∼15 μg m⁻³).     

Influence of pesticides on acetylene reduction and growth of microorganisms in an organic soil 1

Abstract

The effects of 32 pesticides at two concentrations on acetylene reduction (non‐symbiotic nitrogen fixation), nitrogen fixers, bacteria and fungi in an organic soil were assessed. None of the pesticide treatments suppressed C H reduction as compared to controls. No significant inhibition of the population of non‐symbiotic nitrogen fixers occurred. However, stimulatory effects were observed with treatments of fensulfothion, fonofos, oxamyl, DD^R , Telone^R and Telone C^R . Bacterial and fungal populations showed temporary declines but all recovered within 7 days to levels similar to or higher than those in the controls.     

载钴活性焦对As(V)的吸附性能与去除效果

使用沉淀负载法制备了载钴活性焦,并研究了溶液pH值、反应时间、As(V)初始浓度以及共存阴离子等对载钴活性焦吸附去除水环境中As(V)的影响。结果表明,(1)载钴后活性焦的比表面积和孔容积分别提高了20.87%和43.47%;(2)载钴活性焦对As(V)最佳吸附pH值为4.0,当As(V)的初始浓度为10 mg/L时,As(V)去除率可达97%;(3)吸附过程符合准二级动力学模型(k2=0.66,R2=0.96),吸附等温线为Freundlich型(kF=8.227,1/n=0.396,R2=0.97);(4)稳定性实验验证了载钴活性焦的稳定性,钴不易脱附,最大脱附率仅为0.145%。     

Application of HYDRUS 1D model for assessment of phenol–soil adsorption dynamics

Laboratory-scale batch, vertical, and horizontal column experiments were conducted to investigate the attenuative capacity of a fine-grained clayey soil of local origin in the surrounding of a steel plant wastewater discharge site in West Bengal, India, for removal of phenol. Linear, Langmuir, and Freundlich isotherm plots from batch experimental data revealed that Freundlich isotherm model was reasonably fitted (R ²?=?0.94). The breakthrough column experiments were also carried out with different soil bed heights (5, 10, and 15 cm) under uniform flow to study the hydraulic movements of phenol by evaluating time concentration flow behavior using bromide as a tracer. The horizontal migration test was also conducted in the laboratory using adsorptive phenol and nonreactive bromide tracer to explore the movement of solute in a horizontal distance. The hydrodynamic dispersion coefficients (D) in the vertical and horizontal directions in the soil were estimated using nonlinear least-square parameter optimization method in CXTFIT model. In addition, the equilibrium convection dispersion model in HYDRUS 1D was also examined to simulate the fate and transport of phenol in vertical and horizontal directions using Freundlich isotherm constants and estimated hydrodynamic parameters as input in the model. The model efficacy and validation were examined through statistical parameters such as the coefficient of determination (R ²), root mean square error and design of index (d).     

Evaluation of the mobility of c14‐labelled pesticides in soils by thin layer chromatography using a linear analyser

Abstract

The mobility of seven pesticides in a chromic cambisol soil was studied by soil thin layer chromatography. Pesticide mobilities were determined by means of conventional autoradiographs of the chromatograms, as well as from sequential series of curves and images of the pesticide spots provided by a linear analyser. The R _f values obtained from the autoradiographs and those provided by the linear analyser were quite consistent. Based on such values, pesticide mobility decreased in the following order: acephate > fluometuron > atrazine > ethofumesate > metolachlor > diazinon > glyphosate. According to the mobility scale proposed by Helling and Turner (1968), acephate is highly mobile; atrazine, fluometuron, ethofumesate and metolachlor are moderately mobile; diazinon is slightly mobile; and glyphosate is immobile. The images provided by the linear analyser allow to determine the R _f values for the zones of maximum activity in the pesticide spots (R _f ^max), as well as the activities of different spot zones and those corresponding to R _f and R _f ^max. The results obtained show the image analyser to provide more expeditious R _f measurements from the chromatograms and open up new prospects for using soil TLC to investigate pesticide mobility.     

Tube-Immunoassay for Rapid Detection of Carbaryl Residues in Agricultural Products

An antibody-based rapid, quantitative, and qualitative tube enzyme-linked immunosorbent assay (tube-ELISA) was developed and used to determine carbaryl (1-naphthyl methylcarbamate) residues in agricultural products (apple, Chinese cabbage, rice, and barley). The tube-ELISA is a competitive immunoassay in which the antibody is coated in the polystyrene tube, with a dynamic range between 0.7 and 46.3 μg kg^?1. Carbaryl was extracted from each agricultural sample by hand-shaking with methanol and examined for application to on-site analysis. After the liquid extraction, the sample extracts diluted with buffer were analyzed by rapid tube-ELISA directly. The overall test time was around 15–30 min, including sample preparation and assay performance. The results obtained from tube-ELISA correlated well with high-performance liquid chromatography (R ² > 0.9). The study shows that tube-ELISA is useful as a quality control tool and can be used to quantitatively detect carbaryl as well.     

Enantioselective toxic effects and biodegradation of benalaxyl in Scenedesmus obliquus

Enantioselectivity in ecotoxicity and biodegradation of chiral pesticide benalaxyl to freshwater algae Scenedesmus obliquus was studied. The 96 h-EC₅₀ values of rac-, R-(−)-, S-(+)-benalaxyl were 2.893, 3.867, and 8.441 mg L⁻¹, respectively. Therefore, the acute toxicities of benalaxyl enantiomers were enantioselective. In addition, the pigments chlorophyll a and chlorophyll b, antioxidant enzyme activities catalase (CAT) and superoxide dismutase (SOD) as well as lipid peroxide malondialdehyde (MDA) were determined to evaluate the different toxic effects. Chlorophyll a was induced by S-(+)-benalaxyl but inhibited by R-(−)-benalaxyl at 1 mg L⁻¹. Chlorophyll b were both induced at 1 mg L⁻¹, but S-(+)-form was fourfold higher than R-(−)-form. S-(+)-benalaxyl inhibited more CAT activities at 3 mg L⁻¹ and 5 mg L⁻¹, induced less SOD activity and MDA content at 5 mg L⁻¹ than R-(−)-benalaxyl. Based on these data, enantioselectivity occurred in anti-oxidative stress when S. obliquus response to benalaxyl. In the biodegradation experiment, the half-lives of S-(+)-benalaxyl and R-(−)-benalaxyl were 4.07 d and 5.04 d, respectively, resulting in relative enrichment of the R-(−)-form. These results showed that toxic effects and biodegradation of benalaxyl in S. obliquus were enantioselective, and such enantiomeric differences must be taken into consideration in pesticide risk.