Field Studies on 32P Movement and P Leaching from Flooded Paddy Soils in the Region of Taihu Lake, China

Field experiments were done in two sites, Yixing and Changshu, Jiangsu province, China, to study P movement and leaching in flooded paddy soils. P movement in soil was investigated by using the KH₂ ³²PO₄ tracker method, and the amount of P leached from the soil layer in different depths was estimated by measuring P concentrations in the soil solution and saturated hydraulic conductivities in field. Determination was done about one month after P application. There was 46% and 42% of total ³²P retained in the 0–5cm layer of soil in the Yixing site and in the Changshu site respectively. The ³²P retained in the 25–30 cm layer was only about 1–2% of the total ³²P added. Furthermore, 8.01% of ³²P in the soil of Yixing site and 16.8% of ³²P in the soil of Changshu site was lost from the layer 0–30cm soil. The seasonal amounts of P leached from the top soil layer and from bottom layer are about 4.5–5.8% and 1.6–2.1% of the total P application, respectively. Changes of total P concentrations in soil solutions during rice growth showed that the fertilizer P applied before flooding of the paddy fields suffered a flash leaching loss and a slow leaching loss. We concluded that the fertilizer P could quickly move in the flooded paddy rice field and parts of it can enter into surface water and ground water. Unless the P application is well managed the risk of P loss and consequently environmental pollution exist.     

Effect of biogeochemical interactions on bioaccessibility of arsenic in soils of a former smelter site in Republic of Korea

The total concentration-based regulations for soil remediation do not consider the possible changes in bioaccessibility of remaining arsenic (As) in soils due to biogeochemical interactions after remediation. This study used As-contaminated soil and pore water samples that were collected from the rice paddy and forest/farmland located in the vicinity of a former smelter site in Republic of Korea to elucidate the changes in As bioaccessibility due to biogeochemical interactions. Bioaccessibility and chemical forms of As in soils were determined by using an in vitro method and sequential extraction, respectively, and soil microbial community was evaluated. Bioaccessibility of As in the rice paddy soil samples was higher than that in the forest/farmland soil samples. This could be attributed to relatively higher dependence of bioaccessible As in the rice paddy soils on the soil concentration of iron (Fe), aluminum, or manganese, which could lead to greater changes in bioaccessible As via reductive dissolution. The strong linear relationship (R ² = 0.90, p value ≤0.001) between the pore water As and Fe concentrations, and the greater portion of bacterial species related to reductive dissolution of Fe oxides in the rice paddies can support the higher As bioaccessibility promoted by reductive dissolution. Therefore, it is necessary to consider the potential changes in the bioaccessible As due to biogeochemical interactions in remediation of As-contaminated soils, particularly when soils are likely to be reused under reductive dissolution-promoting conditions (e.g., flooded conditions).     

土壤水溶态铜对小白菜的毒害效应及其预测模型

土壤中铜(Cu)重金属的生物毒性/有效性主要取决于它们在土壤液相中含量和土壤溶液的性质。探寻土壤有效态Cu的生物毒害效应,表征量化其与土壤溶液性质关系,可为土壤Cu的环境风险评价提供参考。选取17种典型农田土壤,探讨了有效态Cu(土壤孔隙水以及CaCl_2浸提态)对小白菜生长的毒性效应及其预测模型。结果表明:土壤孔隙水中Cu对小白菜生长10%抑制的毒性阈值值(EC_(10))和50%抑制的毒性阈值(EC_(50)),最大值与最小值相差为14.7和14.6倍;同样,对于CaCl_2提取态Cu的EC_(10)和EC_(50),最大值与最小值相差12.7和7.7倍,表明土壤溶液性质对水溶性Cu对小白菜的毒性阈值影响很大。建立了土壤溶液的重要因子(溶解性有机碳、土壤溶液pH值、电导率、全硫含量、Ca~(2+)、Mg~(2+)、K~+、Na~+)和水溶性Cu阈值之间的多元回归关系,结果显示,土壤溶液性质可以较好地预测水溶性Cu对小白菜的毒性阈值。同时,土壤溶液中Mg~(2+)、K~+和S的含量是控制孔隙水中Cu对小白菜生长毒性的最重要因子,单一的S能分别解释34%的EC_(10)变异,K~+解释26%的EC_(50)变化。本研究结果可为陆地环境中水溶性Cu的风险评价提供基础。     

不同价态铬在不同水分条件下的生物有效性及其对水稻的毒性

氧化还原过程在铬的形态转化中起了重要作用,而铬形态的转化能够影响其生物有效性及毒性。通过温室土培试验研究了六价铬(Cr(Ⅵ))与三价铬(Cr(Ⅲ))在淹水与不淹水条件下在土壤溶液中的动态变化及水稻对其吸收的变化。结果表明,土壤中添加Cr(Ⅲ)时,土壤溶液中检测不出Cr;而随着土壤中添加Cr(Ⅵ)浓度的增加,土壤溶液中Cr(Ⅵ)的浓度增加,但是溶液中检测不出Cr(Ⅲ);淹水处理总体上降低了土壤溶液中Cr(Ⅵ)的浓度。而土壤添加Cr(Ⅲ)、Cr(Ⅵ)和水分处理对土壤溶液p H没有显著影响,p H在7.08.0之间变动。土壤添加Cr(Ⅵ)处理的水稻中,只有90 mg·kg-1Cr(Ⅵ)淹水处理的水稻成活,而其余处理水稻没有成活。土壤中添加Cr(Ⅲ)处理,水稻幼苗生物量随Cr(Ⅲ)浓度的增加而显著降低;除了200mg·kg-1Cr(Ⅲ)处理外,其余淹水处理的水稻幼苗生物量明显高于不淹水处理的。土壤添加Cr(Ⅲ)处理的水稻,在不淹水条件下水稻空壳率比较高,淹水条件下,随着土壤中添加Cr(Ⅲ)浓度水平的增加,水稻各部位Cr含量有增加的趋势,但增加不显著,秸秆最高Cr含量达到33.80 mg·kg-1,籽粒中Cr含量最高0.30 mg·kg-1。土壤固定Cr(Ⅲ)的能力远强于Cr(Ⅵ),添加Cr(Ⅵ)处理的土壤溶液中Cr(Ⅵ)的浓度很高,对水稻表现出较强的生长抑制。     

Mobility and adsorption of the triketone herbicide mesotrione in the soil of corn crops

The triketone herbicide mesotrione has been applied pre‐emergence at the dose of 150 g a.i. ha^?1 on corn fields grown within the same period of time at different sites on clay, loam, sandy loam or sandy soils. During the crops and one month after the corn harvest, the mobility of mesotrione has been measured in the 0–20 cm surface soil layer, soil samples being taken in the 0–2,2–4,4–6,6–8, 8–10, 10–15 and 15–20 cm surface soil layers. During the first month after the treatment, mesotrione remained in the 0–2 cm surface soil layer. Thereafter, mesotrione was at a higher concentration in a 2 cm‐thick soil layer which progressively moved down in the clay, loam and sandy loam soils. In the sand soil, mesotrione moved down as a uniform diffusion, its concentration being similar in all the 2 cm‐thick layers of the 0–10 cm soil surface layer. Low mesotrione residues (6–10 ug kg^?1 dry soil) attained the 10–15 cm layer faster in the clay and sand soils than in the loam and sandy loam soils. Mesotrione was not detected in the 15–20 cm soil layer of the loam and sandy loam soils, but well in the sand and clay soils. In the soils of the corn crops mesotrione thus mainly remained in the 0–10 cm surface soil layer. This low mobility and depth of penetration conjugated to the rate of mesotrione soil degradation explain why there was no movement of mesotrione toward the deeper soil layers. The adsorption of mesotrione was greatest on the soils recently treated with organic fertilizers, and having a loam or sandy loam texture. The adsorption coefficients explained the lower mobility and the greatest persistence of mesotrione in these soils.     

Shifts in Microbial Communities,Microbial Biomass and Organic Matter Mineralization for Three Mediterranean Soils Contaminated By Metals

Microbial communities (phospholipid fatty acid pattern, bacterial growing strategies, eco-physiological index (EPI) and total bacteria counts, as a number of heterotrophic cuhurable bacteria), substrate-induced respiration (SIR), and nitrogen mineralization were studied in three Mediterranean soils at three different depth levels (A, B and C). Soils were experimentally treated with a final concentration of 1000 ppm of trace metals (Cu²⁺, Zn²⁺, Al³⁺, Fe²⁺, Pb²⁺, Ni²⁺, Mn²⁺, Cr³⁺ and Cd²⁺). Soils were stored in 571 plastic containers for one year, and watered with 1001 during this period. Leachate was recovered through a bottom tap. Samples of the three depths were studied. Soil microbial communities showed different effects to other studies presented in the literature, but carried out on non-Mediterranean soils. Dramatic differences were found between treated soils and untreated ones, but not between soils or horizons. the treated soil displayed a decrease in CFUs, SIR N-mineralization and EPI together with a dominance of r-growing strategists. the relative moles percent of several PLFAs, especially 15:0, 16: 1ω7, cy17: 0, br18:0 and 18: 1ω7 decreased because of the pollution of soils, whereas 10Me16, 18:2ω6, cy19:0, i16:0 and br17:0 showed higher values than in untreated soils.     

Field studies on 32P movement and P leaching from flooded paddy soils in the region of Taihu Lake, China

Field experiments were done in two sites, Yixing and Changshu, Jiangsu province, China, to study P movement and leaching in flooded paddy soils. P movement in soil was investigated by using the KH2 32PO4 tracker method, and the amount of P leached from the soil layer in different depths was estimated by measuring P concentrations in the soil solution and saturated hydraulic conductivities in field. Determination was done about one month after P application. There was 46% and 42% of total 32P retained in the 0-5cm layer of soil in the Yixing site and in the Changshu site respectively. The 32P retained in the 25-30 cm layer was only about 1-2% of the total 32P added. Furthermore, 8.01% of 32P in the soil of Yixing site and 16.8% of 32P in the soil of Changshu site was lost from the layer 0-30 cm soil. The seasonal amounts of P leached from the top soil layer and from bottom layer are about 4.5-5.8% and 1.6-2.1% of the total P application, respectively. Changes of total P concentrations in soil solutions during rice growth showed that the fertilizer P applied before flooding of the paddy fields suffered a flash leaching loss and a slow leaching loss. We concluded that the fertilizer P could quickly move in the flooded paddy rice field and parts of it can enter into surface water and ground water. Unless the P application is well managed the risk of P loss and consequently environmental pollution exist.     

Influence of uraniferous black shales on cadmium,molybdenum and selenium in soils and crop plants in the Deog-Pyoun-g area of Korea

The influence of naturally occurring uraniferous black shales on cadmium, molybdenum and selenium concentrations in soils and plants is examined. The possible implications of element concentrations to animal and human health are considered for the Deog-Pyoung area. Geochemical surveys have been undertaken within 13 river tributary valleys in the area underlain by uraniferous black shales and black slates or grey chlorite schists. Sampling of rocks, soils and plants has been carried out along transect lines within each valley. Samples were analysed for trace elements by Inductively Coupled Plasma Atomic Emission Spectrometry (ICP-AES) and for uranium by Neutron Activation Analysis (NAA). Soil pH, cation exchange capacity, loss on ignition and particle size distribution have been measured for selected samples. Average trace element concentrations of the Okchon uraniferous black shales were 6.3 μg g⁻¹ Cd, 136 μg g⁻¹ Mo and 8.6 μg g⁻¹ Se. Soils derived from these rocks tend to reflect their extreme geochemical composition. Trace element concentrations in alluvial soils derived in part from these black shales averaged 1.2 μg g⁻¹ Cd, 20 μg g⁻¹ Mo and 1.5 μg g⁻¹ Se. Trace element concentrations in plants were found to be influenced by those of soils. Cadmium accumulated in tobacco leaves up to 46 μg g⁻¹ (D.M.) and leafy plants such as lettuce contain up to 0.5 μg g⁻¹ Se (D.M.). In addition to total concentrations in soils, soil pH is a major factor influencing uptake of Mo into crop plants and soil texture for Se. Concentrations of trace elements in plants also varied between plant species. The relative concentrations of Cd were found to vary in the order tobacco > lettuce > red pepper > rice grain. Elevated concentrations of Cd in crop plants and in tobacco may possibly have deleterious effects on human health in this area. The low Cu:Mo ratio in rice stalk of 2.65:1 may be associated with disturbed Cu metabolism in ruminant animals which regularly consume this material.     

Attenuation of metal species in acidic solutions using bentonite clay: implications for acid mine drainage remediation

A laboratory batch experimental study has been carried out to evaluate the adsorption capacity of selected metal species in acid mine drainage (AMD) by bentonite clay. Bentonite clay was mixed with simulated AMD at specific solid–liquid (S/L) ratios and agitated in a reciprocating shaker and adsorption of selected toxic metals assessed over time. Cation exchange capacity varied from 1140 to 1290 meq kg^?1. Contact of AMD with bentonite leads to increase in pH and a possible reduction in electrical conductivity and total dissolved solids. At constant agitation time of 60 min, the pH increased with dosage of bentonite. Removal of Mn²⁺, Al ³⁺, and Fe³⁺ was observed to be greatest at 60 min of agitation. Bentonite clay exhibits high adsorption for Al³⁺ and Fe³⁺ at concentration less than 300 mg L^?1, while the capacity for Mn²⁺ was observed to be lower. Adsorption capacity for SO₄^2? was low with a great percentage of the SO₄^2? remaining in solution. Adsorption capacity of bentonite with more complex formulated AMD and gold tailing leachates was low for Fe³⁺, Al³⁺, and Mn²⁺. This indicates that optimum adsorption of bentonite clay is dependent on the chemistry of the AMD and its application might be site specific.     

Effects of Zn and ZnO nanoparticles and Zn2+ on soil enzyme activity and bioaccumulation of Zn in Cucumis sativus

The increased production and commercial use of nanoparticles (NPs), combined with a lack of regulation regarding their disposal, may result in the unwanted introduction of NPs to soils. In this study, the toxicity on soil enzyme activity and growth of Cucumis sativus treated with Zn or ZnO NPs was evaluated in pot soils. Specifically, C. sativus was cultivated in soils treated with Zn NPs, ZnO NPs or Zn²⁺ for eight weeks, after which the treatment effects on biomass and bioaccumulation were evaluated. In addition, the treatment effects on soil dehydrogenase, β -glucosidase and acid phosphatase were investigated. Soil enzyme activities were influenced by all treatments, with an especially large decrease in dehydrogenase activity in response to Zn²⁺ treatment. Biomass and root length also decreased in response to Zn²⁺ treatment. Finally, the Zn contents of C. sativus were much lower in the Zn NP and ZnO NP treatment groups than in the Zn²⁺ treatment group. Therefore, toxicity on soil microbial activity may have a greater influence than phytotoxicity due to immobilisation and aggregation of NPs in the soil.     

Hydraulic properties of typical salt-affected soils in Jiangsu Province, China

Every year about 1,500 ha of land is reclaimed from the sea along the coastline of Jiangsu Province, China. It is important to characterize the hydraulic properties of this reclaimed land to be able to predict and manage salt and water movement for amelioration of these saline soils. In this paper, we report hydraulic properties of these salt-affected soils. The pressure-plate method, constant head method, the crust method and Klute's method were used in this study. The saturated hydraulic conductivities of the soils ranged from 128.66 to 141.26 cm/day and decreased with increasing soil depth. The unsaturated hydraulic conductivities followed an exponential function of pressure head. The soil water retention curves were similar for three soil layers in the soil. The saturated water content, field capacity and wilting point decreased with increasing soil depth. Plant available water contents of the three layers in the soil profile were 0.21, 0.20 and 0.19 cm³/cm³, respectively. The unsaturated soil water diffusivity of the studied soils ranged from 0.07 to 10.46 cm²/min, and was related to the water content via an exponential relationship.     

Gypsum addition to soils contaminated by red mud: implications for aluminium, arsenic, molybdenum and vanadium solubility

Red mud is highly alkaline (pH 13), saline and can contain elevated concentrations of several potentially toxic elements (e.g. Al, As, Mo and V). Release of up to 1 million m³ of bauxite residue (red mud) suspension from the Ajka repository, western Hungary, caused large-scale contamination of downstream rivers and floodplains. There is now concern about the potential leaching of toxic metal(loid)s from the red mud as some have enhanced solubility at high pH. This study investigated the impact of red mud addition to three different Hungarian soils with respect to trace element solubility and soil geochemistry. The effectiveness of gypsum amendment for the rehabilitation of red mud-contaminated soils was also examined. Red mud addition to soils caused a pH increase, proportional to red mud addition, of up to 4 pH units (e.g. pH 7 → 11). Increasing red mud addition also led to significant increases in salinity, dissolved organic carbon and aqueous trace element concentrations. However, the response was highly soil specific and one of the soils tested buffered pH to around pH 8.5 even with the highest red mud loading tested (33 % w/w); experiments using this soil also had much lower aqueous Al, As and V concentrations. Gypsum addition to soil/red mud mixtures, even at relatively low concentrations (1 % w/w), was sufficient to buffer experimental pH to 7.5–8.5. This effect was attributed to the reaction of Ca²⁺ supplied by the gypsum with OH^? and carbonate from the red mud to precipitate calcite. The lowered pH enhanced trace element sorption and largely inhibited the release of Al, As and V. Mo concentrations, however, were largely unaffected by gypsum induced pH buffering due to the greater solubility of Mo (as molybdate) at circumneutral pH. Gypsum addition also leads to significantly higher porewater salinities, and column experiments demonstrated that this increase in total dissolved solids persisted even after 25 pore volume replacements. Gypsum addition could therefore provide a cheaper alternative to recovery (dig and dump) for the treatment of red mud-affected soils. The observed inhibition of trace metal release within red mud-affected soils was relatively insensitive to either the percentage of red mud or gypsum present, making the treatment easy to apply. However, there is risk that over-application of gypsum could lead to detrimental long-term increases in soil salinity.     

Phosphorus Losses to Water from Lowland Rice Fields under Rice–Wheat Double Cropping System in the Tai Lake Region

To assess P losses to surface water by runoff during the rice season and by drainage flow during the winter wheat season, serial field trials were conducted in different types of paddy soils in the Tai Lake Region (TLR) during 2000 and 2001. Four P application rates were set as 0 (CK), 30, 150, and 300 kg P/hm² for flooded rice trials and 0 (CK), 20, 80, 160 kg P/hm² for winter wheat trials respectively. Field experiments were done in two locations with a plot size of 30 m² and four replications in a randomized complete block design. A simplified lysimeter was installed for each plot to collect all the runoff or drainage flow from each event. Total P (TP) losses to surface water during rice season by runoff flow from four treatments were 150 (CK), 220 (T30), 395 (T150), 670 (T300) g P/hm² in year 2000, and 298, 440, 1828, 3744 g P/hm² in year 2001 respectively in Wuxi station, here the soil is permeable paddy soil derived from loam clay deposit. While the losses were 102, 140, 210, 270 in year 2000, and 128, 165, 359, 589 g P/hm² in year 2001 respectively in Changshu station, here the soil is waterlogged paddy soil derived from silt loam deposit. During the winter wheat season, total P lost from the fields by drainage flow in the four treatments were 253 (CK), 382 (T20), 580 (T89), 818 (T160) g P/hm² in year 2000–2001, and 573.3, 709.4, 1123.2, 1552.4 g P/hm² in year 2001–2002 at the Wuxi station. While these were 395.6, 539.1, 1356.8, 1972.1 g P/hm² in year 2000–2001, and 811.5, 1184.6, 3001.2, 5333.1 g P/hm² in year 2001–2002 at the Changshu station. Results revealed that P fertilizer application rates significantly affected the TP concentrations and TP loads in runoff during the rice season, and by drainage flow during the winter wheat season. Both TP loads were significantly increased as the P application rate increases. The data indicate that TP losses to surface water were much higher during the winter wheat season than during the rice season in two tested sites. The data also reveal that the annual precipitation and evaporation rate affected the soil P losses to surface water significantly. Year 2000 was relatively dried with higher evaporation thus P losses to water by both runoff and drainage flow were less than in year 2001 which was a relatively wet year with lower evaporation. Results indicate that texture, structure of the soil profile, and field construction (with or without ridge and deep drains) affected soil P losses to surface water dramatically. Annual possible TP lost to water at the application rate of 50 kg P/hm² year tested in TLR were estimated from 97 to 185 tones P from permeable paddy soils and 109–218 tones P from waterlogged paddy soils. There was no significant difference of TP lost between the CK and the T50 treatments in both stations, which indicate that there is no more TP lost in field of normal P fertilizer application rate than in control field of no P fertilized. Much higher TP lost in runoff or drainage flow from those other P application rates treatments than from the T50 treatment, which suggest that P losses to surface water would be greatly increasing in the time when higher available P accumulation in plough layer soil in this region.     

Heavy metal concentration in soil and woody plants in a quarry

This study determined the concentration of three heavy metals zinc (Zn), lead (Pb), and cadmium (Cd) in soil and in a woody plant species, Milicia excelsa, at Ishiagu quarry, Nigeria. The highest soil concentrations of Zn, Pb, and Cd in soil were obtained at 1?m from the quarry site. In M. excelsa, the highest concentrations of Zn, Pb, and Cd were 3.12–9.1, 3.9–6.01, and 0.51–1.12?mg?kg^?1, respectively. There were significant positive correlations between Cd and Zn (r?=?0.963) and Cd and Pb (r?=?0.974) in plants as well as between Cd and Pb (r?=?9.84) in soil. The level of Cd in soil reflected significant pollution compared to average global concentrations in soils.     

Heavy metals in soils and crops in Southeast Asia 2. Thailand

A reconnaissance soil geochemical and concomitant plant survey based on 318 soil (0-15 cm) and 122 plant samples was used for the assessment of heavy metal pollution of agricultural soils and crops of Thailand. Arsenic (As), cadmium (Cd), cobalt (Co), chromium (Cr), copper (Cu), mercury (Hg), nickel (Ni), lead (Pb) and zinc (Zn) were determined in soils using aqua regia digestion, and in plants using nitric acid digestion. Organic carbon (C), pH, electrical conductivity (EC) and available phosphorus (P) were determined on the soil samples using appropriate procedures. Results indicated that concentrations of heavy metals varied widely among the different regions of Thailand. Regression analysis between the concentrations of metals in soil (aqua regia extractable) and edible plant parts indicated a small but positive relationship for Cd in all the plants sampled in the survey (R2 = 0.081, p < 0.001). There was also a positive relationship between soil and plant Cd concentrations in rice (R2 = 0.242, p < 0.010), and negative relationships for Zn in rice (R2 = 0.385, p < 0.001), and Cu (R2 = 0.355, p < 0.001) and Zn (R2 = 0.122, p < 0.026) in glutinous rice. Principal component analysis of the soil data suggested that concentrations of As, Co, Cr, Cu, Hg, Ni and Pb were strongly correlated with concentrations of Al and Fe, which is suggestive of evidence of background variations due to changes in soil mineralogy. Thus, the evidence for widespread contamination of soils by these elements through agricultural activities is not strong. On the other hand, Cd and Zn were strongly correlated with organic matter and concentrations of available and aqua regia extractable P. This is attributed to input of contaminants in agricultural fertilisers and soil amendments (e.g. manures, composts).     

Relationships between distributions of longevous population and trace elements in the agricultural ecosystem of Rugao County,Jiangsu, China

Soil, plant, and water, as well as trace elements they contain, can influence human health through the food chain. A survey was conducted on distributions of trace elements in soils, plants, and drinking water in Rugao County, Jiangsu Province, China, an agricultural area with a high level of centenarians and nonagenarians. The ratio of people over 90 years old per 100,000 inhabitants (90-rate) based on village (about 4,000 residents in 4 km²) was correlated with trace elements in soil, drinking water, and rice by means of correlation analysis and/or principal component analysis. Although the average 90-rate in the whole area was as high as 277, the rates were not uniform across the entire region. The 90-rate in the area of loamy and strongly-developed Anthrosols and Cambosols was about 330, significantly higher than the 255 in the areas of sandy and strongly-developed Cambosols and of clayey and weakly-developed Cambosols. The concentrations of available Se, B, Ni, and Mo in soils of the area with the high 90-rate were markedly greater than those in the area with the low 90-rate. This was demonstrated by highly positive correlations between the 90-rate and available Se (r = 0.33), B (r = 0.21), Ni (r = 0.17) and Mo (r = 0.17) at the p < 0.01 level and high loadings of available Se (0.851), B (0.535), Ni (0.594) and Mo (0.394) in the longevous factor. Similar relationships between the available elements in soils and elements in water and rice were found. These results suggest that: (1) the available forms of elements in soil were more crucial to elemental bio-availability in the ecosystem and human health than total elements in soil; and (2) the element association above might have affected the 90-rate positively and could be an important environmental geochemical factor influencing the longevity of humans.     

Oxidized multiwalled carbon nanotubes modified with 2-(2-hydroxy-5-nitrophenyl)-4,5-diphenyl imidazole for solid phase extraction and preconcentration of some metal ions

In this work, a new procedure for the enrichment of the trace amount of Cu²⁺, Ni²⁺, Co²⁺, Pb²⁺, Fe²⁺, and Zn²⁺ ions based on the utilization of multiwalled carbon nanotubes (MWCNT) modified with 2-(2-hydroxy-5-nitrophenyl)-4,5-diphenyl imidazole as chelating agent prior to their determination by flame atomic absorption spectrometry has been described. The influence of effective parameters including pH, amount of ligand and MWCNT, composition of eluent, and coexisting ions on recoveries of understudy metal ions was examined. At the optimum pH of 5.0, all metal ions were quantitatively sorbed onto the proposed solid phase and completely desorbed with 8?mL of 5.0?mol?L^?1 HNO₃. The detection limit of Cu²⁺, Co²⁺, Ni²⁺, Pb²⁺, Fe²⁺, and Zn²⁺ ions was 1.7, 2.4, 2.3, 2.9, 2.8, and 1.4?µg?L^?1, while the preconcentration factor was 63 for Cu²⁺ and 94 for the other metal ions and relative standard deviations between 1.8 less than 3.0%. The proposed procedure was applied for the analysis of various samples.     

Toxic effects of dietary of Al3+ ions in tilapias (Oreochromis niloticus) and protective effect of Zn2+ ion

The lethal effects of aluminum ion (Al³⁺) in tilapia (Oreochromis niloticus) raised in concrete tanks were investigated. Tilapias were fed daily with commercial feed enriched with known concentrations of Al³⁺ and analyzed by differential pulse anodic stripping voltammetry (DPASV). The concentrations of Al³⁺ in feces, water, muscle tissue, viscera, and heads were determined every 3 months for a period of 365 days. The Tilapia head was the most affected tissue by Al³⁺. In general, Al³⁺ bioaccumulation reached the lethal dose (LD₅₀) after 335 days of experiment as follows: 34.9?mg?kg^?1 (muscle tissue), 88.2?mg?kg^?1 (viscera), and 126.9?mg?kg^?1 (head without gills). After determining Cu²⁺, Zn²⁺, and Ca²⁺ by absorption spectrometry, a decrease in the Ca²⁺ concentration was noted in the head during the experimental period. These observations were associated with the occurrence of a decalcification in the bone tissue in the presence of Al³⁺. In contrast, it was found that Zn²⁺ ions may act as a protective agent against Al³⁺-induced contamination.     

Sorption and bioavailability of arsenic in selected Bangladesh soils

The bioavailability of arsenic (As) in the soil environment is largely governed by its adsorption–desorption reactions with soil constituents. We have investigated the sorption–desorption behaviour of As in four typical Bangladeshi soils subjected to irrigation with As-contaminated groundwater. The total As content of soils (160 samples) from the Laksham district ranged from <0.03 to approximately 43 mg kg⁻¹. Despite the low total soil As content, the concentration of As in the pore water of soils freshly irrigated with As-contaminated groundwater ranged from 0.01 to 0.1 mg l⁻¹. However, when these soils were allowed to dry, the concentration of As released in the pore water decreased to undetectable levels. Remoistening of soils to field moisture over a 10-day period resulted in a significant (up to 0.06 mg l⁻¹) release of As in the pore water of soils containing >10 mg As kg⁻¹ soil, indicating the potential availability of As. In soils containing <5 mg As kg⁻¹, As was not detected in the pore water. A comparison of Bangladeshi soils with strongly weathered long-term As-contaminated soils from Queensland, Australia showed a much greater release of As in water extracts from the Australian soils. However, this was attributed to the much higher loading of As in these Australian soils. The correlation of pore water As with other inorganic ions (P, S) showed a strongly significant (P < 0.001) relationship with P, although there was no significant relationship between As and other inorganic cations, such as Fe and Mn. Batch sorption studies showed an appreciable capacity for both As^V and As^III sorption, with As^V being retained in much greater concentrations than As^III.     

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.