Faecal elimination of cypermethrin by cows after pour-on administration: Determining concentrations and measuring the impact on dung beetles

Cattle treatment with antiparasitic drugs is associated with an important risk exposure for dung beetles. Previous studies demonstrated the impact of some avermectin and pyrethroid compounds on several species such as Onthophagus gazella and Neomyia cornicina. However, little information is available regarding the elimination of these compounds in faeces 8 days after a pour-on administration in dairy cows. The present study, utilising a dairy cow model with cypermethrin treatment, demonstrated that concentrations in dry faeces can reach levels of 5?mg?kg^?1 between the first and fourth day after treatment and were present up to 3 months after a single dose of administration at a concentration around 10?µg?kg^?1. Faecal samples were purified with three successive columns (silica gel, anion exchange phase, and basic alumina) and analysed by GC-MS. The limit of quantification of this method was 0.5?µg?kg^?1. The high sensitivity of the method permitted one to see that the risk exposure of cypermethrin to dung beetles is longer than what was noted in the literature. According to other studies, repeated treatment with such agents may lead to the local extinction of dung beetles. Even if the impact of pyrethroid largely depends on the conditions of the ecosystem where the treated cattle are living, adverse effects of these agents may still occur.     

Phytoextraction of lead and its relationship with histidine in six plant species using ICP-MS and HPLC-MS

High-performance liquid chromatography-mass spectrometry and inductively coupled plasma mass spectrometer (ICP-MS) methods were used for determination of histidine and lead in leaves of six plant species taken from industrial areas, including Gaziantep and Bursa cities, Turkey. For extraction of histidine from plant samples, ultrapure water was used at 90°C for 30?min. Using optimum conditions of 0.2?mL?min^?1, 70?V, 15?µL and 20°C, concentrations of histidine (in mg?kg^?1) were found to be between 2 and 9 for Morus L., 6 and 13 for Robinia pseudoacacio L., 2 and 10 for Populous nigra L., 3 and 10 for Thuja, 1 and 11 for Cupressus arizonica and 4 for Cedrus libani. Concentrations of lead were in the ranges of 4–378?mg?kg^?1 for Morus L., 1–122?mg?kg^?1 for R. pseudoacacio L., 1–14?mg?kg^?1 for P. nigra L., 1.6–224?mg?kg^?1 for Thuja (Cupressaceae), 1.5–57?mg?kg^?1 for C. arizonica and 1.8?mg?kg^?1 for C. libani. Related with correlation coefficient, significant linear correlation for Thuja (Cupressaceae) (r?=?0.81) and insignificant linear correlation for P. nigra L. (r?=?0.50) were seen. Further, the leaves of Morus L., Thuja and R. pseudoacacio L. have a potential as biomonitor and/or hyperaccumulator for Pb because the rates of their maximum/minimum concentrations were found higher than 90.     

The potential of Berkheya coddii for phytoextraction of nickel,platinum, and palladium contaminated sites

The study involved assessing the potential of the native plant species (Berkheya coddii) for the phytoextraction of nickel, palladium, and platinum contaminated sites. Plant and soil samples were randomly collected from Barberton area, near Agnes mine, Mpumalanga Province, South Africa. Samples were analysed for total nickel, palladium, and platinum concentrations together with other elements found in the soil and in the plants' roots, and leaves. Soil versus leaves and soil versus roots uptake of these metals by the plant were compared. The mean concentration of nickel in the leaves/canopy was found to be 13,980?±?10,780?mg?kg^?1?dry mass, in the roots it was 2046?±?789?mg?kg^?1 dry mass, and in the soil it was 1040?±?686?mg?kg^?1?dry mass. This resulted in a mean concentration ratio in the leaves to soil of 13.44. The platinum mean concentration in the leaves was 0.22?±?0.15?mg?kg^?1?dry mass, in the roots it was 0.14?±?0.04?mg?kg^?1?dry mass, and in the soil it was 0.04?±?0.03?mg?kg^?1?dry mass. This resulted in a mean concentration ratio in the leaves to soil of 5.5. Palladium was found to have a mean soil concentration of 0.07?±?0.045?mg?kg^?1?dry mass. The mean concentrations in the roots and in the leaves were 0.18?±?0.07 dry mass and 0.71?±?0.52?mg?kg^?1?dry mass, respectively. This gave a mean concentration ratio in the leaves to soil of 10.1 for palladium. Other elements that were found to have a mean concentration ratio in the leaves to soil of around 2.5 or above are sodium, potassium, magnesium, calcium, and sulfur. Berkheya coddii was found to be most efficient in accumulating nickel, palladium, and platinum from the soil. The results for the first time revealed that the plant may have the potential to uptake platinum and palladium; both metals are in the same group of the periodic table as nickel.     

Interaction of selenium and cadmium in wheat at different salinities

Abstract

Interaction of Se up to 8?mg?kg^?1 soil and Cd at 5 and 15?mg?kg^?1 soil in wheat at different salinities was evaluated. Se concentrations in wheat shoots were progressively increased in parallel to Se in soil but decreased by addition of Cd. With increasing salinity, Cd concentrations increased and Se decreased. At low salinity, low addition of Se to the soil reduced Cd accumulation. At moderate and high salinities, only high Se amendment led to decline in Cd uptake, at the expense of reduction in biomass yield. Se at 0.5?mg?kg^?1 soil alleviated the negative effect of Cd on shoot yield.     

Mitigation of glyphosate-based herbicide toxicity in maize (Zea mays L.) seedlings by ascorbic acid

Abstract

The toxicity of glyphosate at 3.6?mg L^?1 to maize seedlings raised from un-treated seeds and the effectiveness of seed pretreatment by soaking in 0.25?mmol L^?1 ascorbic acid (AsA) solution for mitigation of toxicity were evaluated in hydroponic culture. Glyphosate dramatically reduced the growth of roots and photosynthetic pigments in the leaves but increased protein content in the leaves. Superoxide dismutase activity and AsA concentration in the roots were increased, and guaiacol peroxidase (GPOX) activity was unaffected. Pretreatment with AsA improved the dry mass of the roots and shoots, increased the protein content in roots and leaves, and significantly decreased the activity of GPOX in roots. The positive effect of AsA treatment was not associated with more efficient functioning of the antioxidative system.     

Determination of the levels of selected metals in seeds,flowers and fruits of medicinal plants used for tapeworm treatment in Ethiopia

The level of accumulation of selected essential and non-essential metals, namely; Ca, Cu, Fe, Zn, Mn, Cd, Pb, and Cr have been investigated in the seeds, fruits, and flowers of some medicinal plants utilized for tapeworm treatment in Ethiopia and their respective soil samples. These include seed of Cucurbita maxima (Duba), fruit of Embelia abyssinica (Ankoko), flowers of Hagenia abyssinica (Kosso), and fruits of Rosa abyssinica (Kega) and their respective soil samples. A wet digestion procedure with a mixture of conc. HNO₃ and HClO₄ for the plant samples and a mixture of conc. HNO₃, HCl, and H₂O₂ for soil samples were used to solubilize the metals. Ca (1280–12,670?mg?kg^?1) was the predominant metal followed by Fe (104–420?mg?kg^?1), and Zn (18–185?mg?kg^?1) in all the plant materials except for Hagenia abyssinica flower from Hirna in which Mn (16–42?mg?kg^?1) followed by Fe. Among the non-essential toxic metals, Pb was not detected in Cucurbita maxima of Boji, Gedo and Hirna origins and in Rosa abyssinica of Hirna site. Similarly, Cr was not detected in Rosa abyssinica fruits of Boji and Gedo sites. The sampled soils were found to be between strongly acidic to weakly basic (pH: 4.7–7.1). In the soil samples, Ca (8528–18,900?mg?kg^?1) was the most abundant metal followed by Fe (417–912?mg?kg^?1), Zn (155–588?mg?kg^?1), Mn (54–220?mg?kg^?1), Cr (21–105. mg?kg^?1), Cu (11–58?mg?kg^?1), Pb (13–32?mg?kg^?1) and Cd (2.8–4.8?mg?kg^?1). The levels of most of the metals determined in the medicinal plants and the respective soil samples are in good agreement with those reported in the literature and the standards set for the soil by various legislative authorities.     

Effect of sulfur and composted manure on SO4-S,P and micronutrient availability in a calcareous saline–sodic soil

A factorial design with different levels of elemental S and cow manure was used to investigate the effects of S and manure on SO₄-S, P and micronutrient availability in a calcareous saline–sodic soil. The results revealed that the recovery of SO₄-S increased significantly (p≤0.05) in all treatments as elemental S increased, particularly when in combination with manure. The interactional effects of S° and manure application rates resulted in a decrease in soil pH of 0.1 to 0.9 units and increases in soil EC from 0.1 to 2.6 dS m^?1 as result of an increase in the number of oxidisers and the oxidation rate of elemental S. Application of S° in combination with manure led to an increase in soil-available-P (0.6–40 mg kg^?1), DTPA-Zn (0.2–3.9 mg kg^?1) and DTPA-Fe (0.1–5.6 mg kg^?1).     

A novel extraction method for analysing available sulfamethoxazole in soil

A novel extraction method was established to determine the water-extractable (available) content of sulfamethoxazole (SMX) in soil. The SMX imprinted polymers (MIPs) were synthesised and the performance was evaluated by Fourier transform infrared spectroscopy, scanning electron microscopy and binding experiments. Results showed that the MIPs exhibited good selectivity for SMX, so the MIPs were applied as a sorbent. SMX in soil was extracted by water, sorbed from the extract to MIPs and analysed with a high performance liquid chromatography (HPLC) after its desorption from MIPs. Meanwhile, the classic organic solvent extraction was employed to measure the total SMX content in soil. Results showed that when SMX level in spiked soils varying from 1.0–500?μg?kg^?1, the observed recoveries of available SMX contents ranged from 63.27?±?3.11% to 82.11?±?2.77% (n?=?3), while the total SMX varied between 89.59?±?1.65% and 97.64?±?3.92% (n?=?3). The detection limit of the developed method for SMX in soils was 0.05?μg?kg^?1. Available SMX contents in five field soil samples ranged from 0.13 to 4.14?μg?kg^?1, which were only 0.35–25.40% of the respective total SMX contents. Results from this study manifest the importance of the extents of SMX immobilisation with different soils for assessing SMX's ecological and human health risks.     

Heavy metal pollution in soil and plants at bone char site

This study determined the heavy metal concentration in soil and plants at a bone char site in Umuahia, Nigeria. Soil and plant samples collected in a randomized complete block design (RCBD) were analyzed for zinc (Zn), lead (Pb), cadmium (Cd), nickel (Ni), and arsenic (As). The concentration of metals in soil and plants in the vicinity of the bone char site are as follows: Zn (172?mg?kg^?1) and Ni (0.62?mg?kg^?1) in soil were highest at site P₃, Pb (2.37?mg?kg^?1) and As (0.08?mg?kg^?1) at site P₁, and Cd (18.30?mg?kg^?1) at site P₂. In plants, the concentrations of Zn (41.17?mg?kg^?1) and Cd (3?mg?kg^?1) were highest in Albizia ferruginea, Ni in Dialium guineense (0.09?mg?kg^?1), while Pb was in D. guineense (0.08?mg?kg^?1) and Spathodea companulata (0.06?mg?kg^?1). The levels of Zn, Cd, Pb, Ni, and As in soil ranged from 11.2 to 172, 2.68 to 18.2, 0.026 to 2.37, 0.33 to 0.62, and 0.02 to 0.08?mg?kg^?1, respectively. In plants, the concentration of Zn, Cd, Pb, and Ni ranged from 2.01 to 41.17, 0.12 to 3, 0.02 to 0.08, and 0.03 to 0.09?mg?kg^?1, respectively. There were significant correlations between Zn and Cd, and Pb and As in soil. The high concentration of Cd in soil might affect soil productivity.     

Soil biological characteristic,nutrient contents and stoichiometry as affected by different types of remediation in a smelter-impacted soil

ABSTRACT

In order to evaluate the ecological risk reductions of copper (Cu) and cadmium (Cd) and the change of nutrient contents and stoichiometry in a smelter-impacted farmland in Guixi, Jiangxi Province, China, with ～ 800?mg Cu kg^?1 soil and 0.8?mg Cd kg^?1 soil, an three years in situ experiment was conducted. The field trial consisted of 4 ×?5?m plots in a completely randomised block design. Hydroxyapatite was added at 10?g kg^?1 soil and Sedum plumbizincicola, Elsholtzia splendens, and Pennisetum sp. were planted. Post-treatment soil and plant samples were collected annually and analysed for Cu and Cd bioaccessibility, soil carbon: nitrogen: phosphorus (C:N:P), and the stoichiometries of soil β-glucosidase (BG), N-acetylglucosaminidase (NAG), and acid phosphatase (AP) activity levels. The results indicated that the hydroxyapatite treatments significantly reduced Cu and Cd bioaccessibility as well as the ratio of C:P and N:P. Moreover, BG, NAG, and AP activity levels all increased relative to those in untreated soil. Plants may also influence soil BG, NAG, and AP activity. This study demonstrated that in situ Cu and Cd stabilisation by hydroxyapatite and phytoextraction is ecologically safe and can alter soil mineral nutrient ecological stoichiometry and enzyme activity.     

Selenium improves physiological responses and nutrient absorption in wheat (Triticum aestivum L.) grown under salinity

Abstract

Salinity is a serious limiting factor for crop growth and production. The present study was conducted to investigate the response of wheat grown at salinities of 0.12, 0.30 and 0.60?S?m^?1 on soil supplemented with 0, 0.5, 1 and 4?mg?kg^?1 Se as selenite. Chlorophyll a and b, carotenoid contents, Fe, Zn and Se in shoots as well as shoot dry weight were negatively affected by increased salinity. Se had a dual effect: at 0.5?mg?kg^?1, chlorophyll b, proline, and shoot Fe content were increased, catalase activity was stimulated; there was no effect on Zn content and shoot dry weight. At the two higher concentrations, Se led to decreases in chlorophyll content, nutrient concentration, and shoot dry weight. Thus, moderate addition of Se to soil could be a strategy to improve physiological responses and micronutrient status in wheat under salinity stress.     

Persistence of chlorpyriphos in okra (Abelmoschus Esculentus) fruits and soil

Persistence of cypermethrin and chlorpyriphos in okra and soil were studied following the application of pre-mix formulation of insecticides Action 505EC (chlorpyriphos 50%?+?cypermethrin 5%) at single (275?g a.i.?ha^?1) and double dose (550?g a.i.?ha^?1). The average initial deposits of chlorpyriphos in okra were observed to be 0.07 and 0.15?mg?kg^?1 in single and double dose, respectively, which dissipated to 92% after 10 days for both the dosages. Residues of soil under okra crop were found to be 0.15?mg?kg^?1 at the single and 0.36?mg?kg^?1 at the double doses. These residues persisted up to 3 days at single and 5 days at double dose. The half-life (t _1/2) periods of chlorpyriphos on okra and soil were observed to be 0.6 days and 1.9 days for single and double dose, respectively. Residues of chlorpyriphos reached below detectable level (BDL) of 0.01?mg?kg^?1 in okra fruits after 7 days at single dose and in 15 days in double dose. In soil, residues of chlopyriphos persisted up to 5 and 7 days in single and double dose, respectively. Following foliar applications of a insecticide formulation (Action 505EC, (chlorpyriphos 50%?+?cypermethrin 5%) on okra at @ 275 and 550?g active ingredient (a.i.)?ha^?1 resulting in active applications of chlorpyriphos at the rate of 250 and 500?g a.i.?ha^?1 the average initial deposits of chlorpyriphos in okra were observed to be 0.07 and 0.15?mg?kg^?1, respectively. These residue levels dissipated to 92% after 10 days at both the dosages. Residues of soil under the okra crop were found to be 15?mg?kg^?1 at the single and 36?mg?kg^?1 at the double dose. The residues persisted up to 3 days at the single and 5 days at the double dose. The half-life (t _1/2) periods of chlorpyriphos on okra were observed to be 0.6 days for application rates, and 1.9 days for soil. Okra fruits and soil samples collected on the 7th and 15th day after application did not show any chlorpyriphos residues above their determination limits of 0.01 and 0.005?mg?kg^?1, respectively.     

Optimisation of bisphenol A removal from water using chemically modified pine bark and almond shell

The ability of pine bark and almond shells to remove bisphenol A (BPA) from aqueous solutions was evaluated. Samples of these traditional agro-forestry by-products were milled, sieved into different particle size fractions (0.10–0.15 and 1.5–2.0 mm) and submitted to two different types of treatment. Sorption experiments were conducted in a batch system at room temperature and natural pH. Sorption equilibrium was attained after 48 h for all systems under study. Bisphenol A was adsorbed more effectively on the smaller particles of the sorbents. Pine bark and almond shell pretreated with formaldehyde presented higher sorption efficiency (95%), followed by almond shell (87%) and pine bark (82%) washed with hot water. All the sorption isotherms were found to fit a Freundlich equation, with correlation coefficients (R ²) between 0.823 and 0.989. The sorption coefficient (K _F) ranged from 0.06 to 0.74 (mg^1?1/n ·L ^1/n ·g ^?1). These results indicate that utilisation of both materials as an alternative sorbent for the removal of bisphenol A from contaminated waters is promising because they are available in large amounts and have an acceptable cost–efficiency ratio when compared with traditional adsorbents.     

The potential ecological risk of soil trace metals following over five decades of agronomical practices in a semi-arid environment

The concentration and potential ecological risk of Mn, Zn, Cu, and Cd in the surface soils (0–30?cm) belonging to 12 soil profiles and 4 soil types (Vertisols, Chernozems, Calcisols, and Cambisols) from the cultivated soils and the corresponding uncultivated soils were investigated. Long-term cultivation caused a considerable build-up diethylene-triamine pentaacetic acid (DTPA)-extractable Mn (7–55%), and Cd (12–31%) as well as the total form of Zn (3–14%), Cu (8–25%), and Cd (33–78%) in all soil types. Following long-time cropping, total Zn (mean?=?73?mg?kg^?1), Cu (mean?=?33?mg?kg^?1), and Cd (mean?=?3.14?mg?kg^?1) and DTPA Zn (mean?=?1.2?mg?kg^?1) and Cu (mean?=?2.44?mg?kg^?1) were below their maximum allowable limits. However, the average amount of DTPA Cd in the tilled soils (min?=?0.4, max?=?0.75, mean?=?0.55?mg?kg^?1) was above its maximum permissible limit mainly due to the over application of phosphate fertilisers and the pesticides. Considering the potential ecological risk (RI) assessment of the cultivated soils (min?=?44, max?=?70, mean?=?54), the soil types were categorised as low (RI?≤?50) to moderate (50?相似文献   

Physiological and antioxidative response of Brassica nigra (L.) to ZnO nanoparticles grown in culture media and soil

Abstract

To investigate metal nanoparticle-induced phytotoxicity, Brassica nigra seeds were exposed to 50–1000?mg L^?1 ZnO nanoparticles in culture media and 100–1000?mg kg^?1 in soil. Plant length and weight were adversely affected in culture conditions, but with soil the effect was not significant. Determination of the radical-scavenging potential revealed that soil grown plants were less stressed than plants grown on culture medium. The total antioxidant and reducing power potential of soil grown plants were less variable compared to plants grown on culture medium. Total phenolic and flavonoid concentrations varied in plants, which changed with the nanoparticle’s concentrations in medium and soil. High performance liquid chromatography analysis showed that rutin was the major antioxidative molecule that significantly increased in nanoparticles-stressed B. nigra plants.     

Assessment of heavy metals contamination in soils surrounding a gold mine: comparison of two digestion methods

This study investigated two digestion methods (USEPA 3051: microwave, HNO₃ or Hossner: hot plate, HF–H₂SO₄–HClO₄) for heavy metals analysis in contaminated soil surrounding Mahad AD'Dahab mine, Saudi Arabia. Moreover, contamination metal levels were estimated. The Hossner and USEPA 3051 methods showed, respectively, average total contents of 17.2 and 18.1 mg kg^?1 for Cd, 11.6 and 10.6 mg kg^?1 for Co, 45.7 and 34.7 mg kg^?1 for Cr, 1030 and 1100 mg kg^?1 for Cu, 33,300 and 27,400 mg kg^?1 for Fe, 963 and 872 mg kg^?1 for Mn, 33.2 and 22.8 mg kg^?1 for Ni, 791 and 782 mg kg^?1for Pb, and 6320 and 2870 mg kg^?1 for Zn. A lack of significant differences and a high correlation coefficient (>90%) for Cd, Pb and Cu between the two digestion methods suggest that the total-recoverable method (USEPA 3051) may be equivalent to the total-total digestion method (Hossner) for determining these metals in the studied soil. However, significantly higher concentrations of Cr, Fe, Ni and Zn were found by the Hossner method comapred with the USEPA 3051 method. The soil samples have very or extremely high levels of Zn, Cu, Cd and Pb contamination, indicating very high potential ecological risk.     

Retention of 137cesium in acid sulphate soils of South Central Thailand

Adsorption and desorption of ¹³⁷Cs by acid sulphate soils from the Nakhon Nayok province, South Central Plain of Thailand located near the Ongkarak Nuclear Research Center (ONRC) were investigated using a batch equilibration technique. The influence of added limestone (12 and 18 tons ha^?1) on ¹³⁷Cs adsorption–desorption was studied. Based on Freundlich isotherms, both adsorption and desorption of ¹³⁷Cs were nonlinear. A large portion (98.26–99.97%) of added ¹³⁷Cs (3.7?×?10³?7.03?×?10⁵ Bq l^?1) was sorbed by the soils with or without added lime. The higher lime treatments, however, favoured stronger adsorption of ¹³⁷Cs as compared with soil with no lime, which was supported by higher K _ads values. The addition of lime, the cation exchange capacity and pH of the soil increased and hence favoured the stronger adsorption of ¹³⁷Cs. Acid sulphate soils with a high clay content, medium to high organic matter, high CEC, and predominant clay types consisting of a mixture of illite, kaolinite, and montmorillonite were the main soil factors contributing to the high ¹³⁷Cs adsorption capacity. Competing cations such as NH₄ ⁺, K⁺, Na⁺, Ca²⁺, and Mg²⁺ had little influence on ¹³⁷Cs adsorption as compared with liming, where a significant positive correlation between K _ads and soil pH was observed. The ¹³⁷Cs adsorption–desorption characteristics of the acid sulphate soils studied exhibited a very strong irreversible sorption pattern. Only a small portion (0.09–0.58%) of ¹³⁷Cs adsorbed at the highest added initial ¹³⁷Cs concentration was desorbed by four successive soil extractions. Results clearly demonstrated that Nakhon Nayok province acid sulphate soils have a high ¹³⁷Cs adsorption capacity, which limits the ¹³⁷Cs bioavailability.     

Arachis hypogaea derived activated carbon steered remediation of Benzimidazole based fungicide adsorbed soils

Sorption characteristics of the Benzimidazole fungicide Carbendazim were assessed in seven different soils using batch equilibrium method and analysed by UV-Vis spectrophotometer. The values of adsorption co-efficient K_d ranged from 14.3 to 39.8?µg/mL depending upon unique physiochemical properties of soils. Negative values for Gibbs free energy (ΔG) proposed an exothermic and low interaction between Carbendazim and soil samples leading to physiosorption. Statistical analysis showed a negative correlation of soil pH and K_d (R²= ?0.80) and a positive correlation with organic matter (R^2?=?0.77). Activated carbon prepared from Arachis hypogaea (peanut shells) by acid activation for Carbendazim removal from soils was characterised by FTIR spectrometry, indicating the change in functional groups. The highest percentage removal observed was 70% in 5?ppm initial Carbendazim concentration while 65% in 7.5?ppm concentration. This method can be implied in agricultural soils as an efficient and cheap technique for removing the hazardous pesticides from the environment.     

Persistence of the sulfonylurea herbicide iodosulfuron-methyl in the soil of winter wheat crops

On four winter wheat fields grown on soils of different textures in Belgium, 10?g a.i.?ha^?1 of the sulfonylurea herbicide iodosulfuron-methyl-sodium was applied post-emergence in the spring. A procedure was developed for the analysis in field soils of iodosulfuron-methyl 1 and of its metabolites iodosulfonamide 2 and iodosaccharin 3 with a sensitivity limit of 0.3?µg of equivalents of iodosulfuron-methyl 1 kg^?1 dry soil. GC and GC-MS was used after purification of the soil extracts by repeated TLC, and methylation. The results of the chemical analyses were confirmed by means of bioassays using sugar beet as test plants. On a winter wheat crop grown on sandy loam soil of pH 6.2 at Melle, iodosulfuron-methyl-sodium 1 was applied at the beginning of April. The iodosulfuron-methyl 1 soil half-life in the 0–10?cm surface soil layer was 60 days. At the end of June, the sum of the concentrations of the metabolites 2 and 3 in the 0–10?cm surface soil layer attained a maximum corresponding to 27% of the applied dose. Green manures were sown after the harvest of the wheat at the end of August. No phytotoxicity at all was observed during the growth of the green manures, in spite of the very low residues of iodosulfuron-methyl 1 remaining in soil in September and October. At the mid of November, iodosulfuron-methyl 1 and its metabolites 2 and 3 were no more detected in soil. On three other winter wheat crops grown on clay soils of pH of about 8 at Leke, Gistel and Zevekote, iodosulfuron-methyl-sodium 1 was applied at the beginning of May. The soil half-life of iodosulfuron-methyl 1 in the 0–10?cm surface soil layer was between 30 and 44 days. Since the application and until the mid of November, in all the trials made on sandy loam or clay soils, iodosulfuron-methyl 1 (and its metabolites 2 and 3 in the trial made on sandy loam soil) were never detected in the 10–15 and 15–20?cm surface soil layers, indicating their low mobilities in the field soils.     

Contamination and source assessment of metals,polychlorinated biphenyls,and polycyclic aromatic hydrocarbons in urban soils from Addis Ababa,Ethiopia

Urban areas in developing countries are facing vast environmental problems as a result of rapid urbanization and industrialization. Of major concern is the contamination of soils which are increasingly becoming sinks for environmental pollutants. However, to date only little is known about the pollution in the megalopolises of developing countries. The aim of this study was to assess the contamination and potential sources of metals, polychlorinated biphenyls (PCBs) and polycyclic aromatic hydrocarbons (PAHs) in the urban environment of Addis Ababa, the capital of Ethiopia. The investigation revealed the presence of most of the analyzed pollutants in soil and sediment samples with total concentrations (dry wt) of PAHs ranging from 186 to 3150?µg?kg^?1, PCBs from 0.4 to 19?µg?kg^?1, Cu from 14 to 173?mg?kg^?1, Zn from 36 to 440?mg?kg^?1, Pb from 9 to 700?mg?kg^?1, and Ni from 16 to 72?mg?kg^?1. In addition, polyaromatic sulfur heterocycles, typical for oil and petrol residues, were detected in several soil samples. Source identification approaches revealed that Pb, Zn, and Cu are most likely derived from pyrolytic sources, with elevated values in samples related to waste combustion and traffic emissions. Ni is most probably of geogenic origin. For PCBs it is indicated that they are derived from a single source. However, correlations with technical PCB mixtures were inconsistent. PAHs originate from the combustion of biomass, vehicular exhausts, and petrogenic sources.