Zinc sorption–desorption by sand,silt and clay fractions in calcareous soils of Iran

Zinc sorption–desorption by sand, silt and clay fractions of six representative calcareous soils of Iran were measured. Sand, silt and clay particles were fractionated after dispersion of soils with an ultrasonic probe. Zinc sorption analysis was performed by adding eight rates of Zn from 6 to 120 μmol g^?1. For the desorption experiment, samples retained after the measurement of Zn sorption were resuspended sequentially in 0.01 M NaNO₃ solution and shaken for 24 h. Results indicated that Zn sorption by soil fractions increased in the order clay > silt > sand, and correlated negatively with CaCO₃ content and positively with cation exchange capacity (CEC) and smectite content. Results indicated that for all fractions, the Langmuir equation described the sorption rates fairly well. In contrast to sorption, Zn desorption from soil fractions increased in the order sand > silt > clay, and correlated positively with CaCO₃ content, CEC and smectite content. Results showed that parabolic diffusion and two constant equations adequately described the reaction rates of Zn desorption. In general, for all soils studied, the coarser the particle size, the less Zn sorption and more Zn desorption, and this reflects much higher risk of Zn leaching into groundwater or plant uptake in contaminated soils.     

Improving on the Prediction of Cation Exchange Capacity for Highly Weathered and Structurally Contrasting Tropical Soils from Their Fine-Earth Fractions

The roles of fine-earth materials in the cation exchange capacity (CEC) of especially homogenous units of the kaolinitic and oxyhydroxidic tropical soils are still unclear. The CEC (pH 7) of some coarse-textured soils from southeastern Nigeria were related to their total sand, coarse sand (CS), fine sand (FS), silt, clay, and organic-matter (OM) contents before and after partitioning the dataset into topsoils and subsoils and into very-low-, low-, and moderate-/high-stability soils. The soil-layer categories showed similar CEC values; the stability categories did not. The CEC increased with decreasing CS but with increasing FS. Silt correlated negatively with the CEC, except in the moderate- to high-stability soils. Conversely, clay and OM generally impacted positively on the CEC. The best-fitting linear CEC function (R², 68%) was attained with FS, clay, and OM with relative contributions of 26, 38, and 36%, respectively. However, more reliable models were attained after partitioning by soil layer (R², 71–76%) and by soil stability (R², 81–86%). Notably FS's contribution to CEC increased while clay's decreased with increasing soil stability. Clay alone satisfactorily modeled the CEC for the very-low-stability soils, whereas silt contributed more than OM to the CEC of the moderate- to high-stability soils. These results provide new evidence about the cation exchange behavior of FS, silt, and clay in structurally contrasting tropical soils.     

Stabilization of chromium(VI) by hydroxysulfate green rust in chromium(VI)-contaminated soils

Chromium (Cr)-contaminated soils pose a great environmental risk, with high solubility and persistent leaching of Cr(VI). In this study, hydroxysulfate green rust (GR_SO4), with the general formula Fe(II)₄Fe(III)₂(OH)₁₂SO₄·8H₂O, was evaluated for its efficiency in Cr(VI) stabilization via Cr(VI) reduction to Cr(III) in four representative Cr(VI)-spiked soils. The initial concentrations of phosphate buffer-extractable Cr(VI) (Cr(VI)_b) in soils 1, 2, 3, and 4 were 382.4, 575.9, 551.3, and 483.7 mg kg^-1, respectively. Reduction of Cr(VI) to Cr(III) by structural Fe(II) (Fe(II)_s) in GR_SO4 in all studied soils was fast, wherein the application of GR_SO4 markedly decreased the amount of Cr(VI)_b at the Cr(VI)_b/Fe(II)_s stoichiometric mole ratio of 0.33. The kinetics of Cr(VI) reduction by GR_SO4 could not be determined as this reaction coincided with the release of Cr(VI) from soil during the experiment. The concentration of Cr(VI)_b decreased, as the Cr(VI)_b/Fe(II)_s ratio decreased from 0.46 to 0.20, generally to below 10 mg kg^-1. Back-transformation of the generated Cr(III) was examined in the presence of manganese oxide birnessite at the birnessite/initial Cr(III) mole ratio of 4.5. The results of batch tests showed that only 5.2% of the initial Cr(III) was converted to Cr(VI) after two months, while under field capacity moisture conditions, less than 0.05% of the initial Cr(III) was oxidized to Cr(VI) after six months. The results illustrated that remediation of Cr(VI)-contaminated soils would be fast, successful, and irreversible with an appropriate quantity of fresh GR_SO4.     

Amendment of drilling fluid-affected soils with calcium salts

Land disposal of waste drilling fluid is an environmental concern because of the high salt content and the presence of potential toxic elements. A water-based drilling fluid was tested in a laboratory column study to determine the feasibility of leaching excessive salt without mobilizing chromium (Cr). The drilling fluid-affected two Alfisols with similar mineralogy, acidity, and texture were treated with gypsum (CaSO₄ · 2H₂O), calcium carbonate (CaCO₃), or calcium phosphate (CaHPO₄) (0 to 2% of weight). The electrical conductivity (EC) increased and the sodium adsorption ratio (SAR) decreased with increasing Ca-salt concentration. The pH did not vary significantly with the changes in the concentrations of gypsum and calcium phosphate. The pH of the mixtures increased in proportion to the concentration of added calcium carbonate. The hydraulic conductivity increased and the mobility of the soil particles decreased with increasing Ca-salt concentration. The Cr mobility decreased by gypsum and CaCO₃ treatments but it increased by calcium phosphate treatment. The soil with a higher content of organic matter and cation exchange capacity (CEC) showed a higher hydraulic conductivity and lower Cr mobility than the other soils at the same levels of the treatment. The results of this study suggest that the amendment of drilling fluid-affected soils with CaCO₃ and gypsum can enhance the leaching of excessive salt and reduce the Cr mobility. Among loamy soil, those with a higher CEC and organic matter content are more suitable for land disposal of drilling fluid.     

水溶性有机碳在各种粘土底土中的吸附：土壤性质的影响

Clay-rich subsoils are added to sandy soils to improve crop yield and increase organic carbon (C) sequestration; however, little is known about the influence of clay subsoil properties on organic C sorption and desorption. Batch sorption experiments were conducted with nine clay subsoils with a range of properties. The clay subsoils were shaken for 16 h at 4 ^oC with water-extractable organic C (WEOC, 1 224 g C L^-1) from mature wheat residue at a soil to extract ratio of 1:10. After removal of the supernatant, the residual pellet was shaken with deionised water to determine organic C desorption. The WEOC sorption was positively correlated with smectite and illite contents, cation exchange capacity (CEC) and total organic C, but negatively correlated with kaolinite content. Desorption of WEOC expressed as a percentage of WEOC sorbed was negatively correlated with smectite and illite contents, CEC, total and exchangeable calcium (Ca) concentrations and clay content, but positively correlated with kaolinite content. The relative importance of these properties varied among soil types. The soils with a high WEOC sorption capacity had medium CEC and their dominant clay minerals were smectite and illite. In contrast, kaolinite was the dominant clay mineral in the soils with a low WEOC sorption capacity and low-to-medium CEC. However, most soils had properties which could increase WEOC sorption as well as those that could decrease WEOC sorption. The relative importance of properties increasing or decreasing WEOC sorption varied with soils. The soils with high desorption had a low total Ca concentration, low-to-medium CEC and low clay content, whereas the soils with low desorption were characterised by medium-to-high CEC and smectite and illite were the dominant clay minerals. We conclude that WEOC sorption and desorption depend not on a single property but rather a combination of several properties of the subsoils in this study.     

A comparative study of Cd,Cr(III), Cr(VI), Hg,and Pb uptake by minerals and soil materials

The pH dependency of Cd, Cr(III), Cr(VI), Hg, and Pb uptake by 14 different types of minerals and soil materials has been studied. The solids were interacted with metal solutions separately in a batch procedure, and the percentage of metal uptake of different metal-solid combinations was compared and evaluated. The results were quantified by the pH values at which 10, 50 and 90% of the metal uptake took place. Physical and chemical characteristics of the solids were correlated with metal uptake. The results verify the importance of geochemical parameters of soils such as organic content, type of clay mineral, presence of complexing ions, and redox-potential for controlling metal uptake. Retention of Cd, Cr(VI), Hg, and Pb was found to be strongly dependent on organic content of the materials studied. Montmorillonite (in bentonite and smectite) showed the highest uptake of Cd, Cr(III) and Pb among all minerals and soil materials, while illite and kaolinite showed lower uptake than the soils. At low pH, the uptake percentage of Cr(VI) by organic soils was higher than that of any of the other metal ions. The uptake of Hg was low in comparison to other cations, which may be explained by formation of soluble Hg(CI)₂° or Hg(CI)⁴ _2? complexes.     

Influence of applied zinc and organic matter on zinc desorption kinetics in calcareous soils

Zinc (Zn) desorption from an exchange complex to solution, the release of Zn from organic matter (OM), crystalline minerals and other precipitates into the solution phase, is the process that controls Zn mobility in soils. An experiment was conducted to determine the pattern of Zn desorption and the soil characteristics affecting it. Desorption of Zn in 15 calcareous soils from southern Iran, treated with 10 mg Zn kg soil^?1 as zinc sulfate (ZnSO₄?7H₂O) and 10 g organic matter (OM) kg^?1 as feedlot cattle manure, equilibrated and extracted with diethylenetriamine pentaacetic acid (DTPA), was studied. Eight kinetic models were evaluated to describe the rate of Zn desorption of soil extracted with DTPA. There was a rapid rate of desorption during the first 4 h followed by a slower rate during the next 12 h. Two-constant rate and simple Elovich models were determined as the best models describing Zn desorption kinetics. Zinc desorption increased as Zn was applied, whereas it decreased with applied OM. The constants of the simple Elovich (β_s) and two-constant rate equations (a and b) were closely correlated with cation-exchange capacity (CEC), OM and pH, which affect Zn solubility, sorption–desorption and diffusion in soils.     

土壤主要理化性质对湘粤污染农田镉稳定效果的影响

利用盆栽试验研究了稳定剂(石灰、海泡石联合施用)对湖南、广东两省区不同性质土壤上生长的小青菜(Brassica chinensis L.)生物量、重金属吸收以及土壤pH和重金属提取态含量的影响,探讨了影响镉(Cd)稳定修复效果的土壤性质参数。结果表明:施加稳定剂对增加酸性土壤上小青菜生物量效果显著,土壤pH、有机质(OM)、全量Cd和黏粒是影响小青菜生物量变化的主要因素;土壤pH、阳离子交换量(CEC)、OM、黏粒是影响小青菜Cd含量变化的主要因素;土壤pH、CEC、全量Cd和黏粒是影响土壤提取态Cd含量变化的主要因素。     

土壤组分对广东省酸性水稻土磷吸附参数的影响

Soil components affecting phosphate sorption parameters were studied using acid paddy soils derived from basalt, granite, sand-shale and the Pearl River Delta sediments, respectively, in Guangdong Province.For each soil, seven 2.50 g subsamples were equilibrated with 50 mL 0.02 mol L-1 (pH=7.0) of KCl containing 0, 5, 10, 15, 25, 50 and 100 ng P kg-1, respectively, in order to derive P sorption parameters (P sorption maximum, P sorption intensity factor and maximum buffer capacity) by Langmuir isotherm equation. It was shown that the main soil components influencing phosphate sorption maximum (Xm) included soil clay, pH,amorphous iron oxide (Feo) and amorphous aluminum oxide (Alo), with their effects in the order of Alo ＞Feo ＞ pH ＞ clay. Among these components, pH had a negative effect, and the others had a positive effect.Organic matter (OM) was the only soil component influencing P sorption intensity factor (K). The main components influencing maximum phosphate buffer capacity (MBC) consisted of soil clay, OM, pH, Feo and Alo, with their effects in the order of Alo ＞ OM ＞ pH ＞ Feo ＞ clay. Path analysis indicated that among the components with positive effects on maximum phosphate buffer capacity (MBC), the effect was in the order of Alo ＞ Feo ＞ Clay, while among the components with negative effects, OM ＞ pH. OM played an important role in mobilizing phosphate in acid paddy soils mainly through decreasing the sorption intensity of phosphate by soil particles.     

Inhibitory effects of the total and water-soluble concentrations of nine different metals on the dehydrogenase activity of a loess soil

 This study focuses on a comparison of the microbial toxicity of nine metals, including As as a metalloid and two species of Cr. A loess soil [Ap horizon, clay 15.2%, organic C 1.12%, pH(CaCl₂) 7.02] was spiked with 8–12 geometrically increasing doses of the metals. The dehydrogenase assay (2-p-iodophenyl-3-p-nitrophenyl-5-phenyltetrazoliumchloride method) was combined with sorption and solubility experiments. The resulting dose-response curves and sorption isotherms were used to derive total doses that caused definite percentage inhibitions [i.e. effective doses (ED) causing a 10–90% reduction in dehydrogenase activity (dha)] as well as the corresponding toxic solution concentrations causing the same reductions in dha (i.e. effective concentrations; EC₁₀–EC₉₀). Based on total doses, the toxicity decreased in the following order with ED₅₀ values (mg kg^–1) given in brackets: Hg (2.0)>Cu (35)>Cr(VI) (71)>Cr(III) (75)>Cd (90)>Ni (100)>Zn (115)>As (168)>Co (582)>Pb (652). With regard to solution concentrations, toxicity decreased in the order (EC₅₀ in mg l^–1): Hg (0.003)>Pb (0.04)>Cu (0.05)>Cd (0.14)>Zn (0.19)>Cr(III) (0.62)>Ni (0.69)>Co (30.6)>As (55.5)>Cr(VI) (78.1). The retention of the metals by the soil differed strongly. Pb, Cu, and Hg exhibited the highest and Ni, As, and Cr(VI) the lowest sorption constants (Freundlich K values: 2455, 724, 348, 93, 13, and 0.06 mg kg^–1, respectively). The sorptivity of the metals and their microbial toxicity in the aqueous phase were characteristically related: metals with a strong toxic action in the soil solution were adsorbed by the soil to a high degree and vice versa. Therefore, especially for metals with a high inherent toxicity, sorption is an effective way of immobilizing them and temporarily detoxifying soil. Received: 2 July 1998     

Soil slaking sensitivity as influenced by soil properties in alluvial and residual humid tropical soils

Purpose

In the humid Caribbean region characterized by high-intensity tropical rainfall, soil aggregate breakdown and pore blocking due to slaking pressures are major land degradation mechanisms. In this research, we investigated the susceptibility of soils to slaking pressures under rapid wetting as influenced by soil properties and the depositional origin from which the soil is formed using water-stable aggregates (WSAr) and percolation stability (PSc) as indices of the strength of aggregate inter-particle cohesion.

Materials and methods

Wet sieving and percolation stability analyses were employed to investigate WSAr and pore blocking, respectively. The combined effect of soil properties of clay, organic matter (OM), cation exchange capacity (CEC), and exchangeable sodium percentage (ESP) was used to determine the slaking sensitivity score (SSc) of 14 physiogeographically important soils in Trinidad, comprising of nine alluvial and five residual soils.

Results and discussion

Results showed that irrespective of alluvial or residual depositional nature of the parent material, samples had high SSc with an average WSAr of 37.8% and PSc of 6.0 mm/10 min. The linear relationships between SSc with WSAr (r²?=???0.12) and SSc with PSc (r²?=???0.012) of all the 14 soils although negative were weak. Clay content accounted for 94.0% of the variation in CEC in alluvial soils and had strong negative relationships with WSAr (r²?=???0.74) and PSc (r²?=???0.79) in residual soils. Additionally, OM with WSAr (r²?=?0.52) and PSc (r²?=?0.24), and CEC with WSAr (r²?=?0.46) and PSc (r²?=?0.39) showed significant positive linear relationships in residual soil.

Conclusions

The predominantly micaceous and kaolinitic clay mineralogy of these soils, coupled with the low OM contents, increases the proneness of the soils to slaking. This suggests that clay mineralogy is responsible for the high slaking sensitivity rather than clay content or just the depositional origin of the soils. As CEC increases, an accompanying increase in OM is required to increase inter-particle cohesion and to impart partial hydrophobicity, which in turn decreases mineralogically induced susceptibility of individual aggregates to slaking.

     

Treatment of Cr(VI)-spiked soils using sulfur-based amendments

The objective of this research was to assess the hexavalent chromium (Cr(VI)) reducing efficiency of sulfur-based inorganic agents including calcium polysulfide (CPS), iron sulfide (FeS), pyrite (FeS₂) and sodium sulfide (Na₂S) in three soils. An alkaline soil (soil 1), a neutral soil (soil 2) and a slightly acid soil (soil 3) constituted the investigated soils. The soils were spiked with two levels of Cr(VI) (100 and 500 mg Cr(VI) kg^?1 soil) and incubated at field capacity (FC) for one month. Then, CPS, FeS, FeS₂ and Na₂S were added at 0, 5 and 10 g kg^?1 and the concentrations of exchangeable Cr(VI) were measured after 0.5, 4, 48 and 168 h in a batch experiment. The pH and organic carbon content of the soils played predominant role in Cr(VI) self-reduction by the soil itself. Complete self-reduction of Cr(VI) from soils 1, 2 and 3 was achieved at maximum Cr(VI) levels of 1, 50 and 500 mg kg^?1, respectively. Therefore, the concentration of Cr(VI) should not exceed the given levels in order to ensure that Cr(VI) is not released into the environment from contaminated sites. Moreover, decreasing pH in the alkaline soil caused significant increase of Cr(VI) reducing efficiency. Na₂S, CPS and FeS, in contrast to FeS₂, were efficient Cr(VI) reducing agents in all three soils. For all added amendments the following order of Cr(VI) reducing capacity was observed: Na₂S > CPS > FeS > FeS₂ in soil 1, Na₂S ? CPS ~ FeS > FeS₂ in soil 2 and Na₂S ? FeS > CPS ~ FeS₂ in soil 3.     

Grass-induced changes in properties of soils in urban green areas with emphasis on mobility of metals

Purpose

Green areas in urban parks are special ecosystems because of social and ecological benefits.

Materials and methods

We investigated the ecological impacts of green spaces by comparing the properties of soils, with emphasis on metals, in green spaces and bare soil playgrounds in four urban parks in Murcia City (SE Spain).

Results and discussion

Organic matter (OM) contents in green areas are higher than playground soils due to litter decomposition from grass. Cation exchange capacity in green areas ranged from 10 to 14 compared to 2 cmol₊kg^?1 in playground soils, showing the effect of OM (and clay) contents in green areas due to the presence of vegetation. Soil total metal contents in urban parks are below the environmental threshold values for soils in Spain and other European countries, and come from atmospheric deposition and fertilizers application. Diethylenetriaminepentaacetic acid (DTPA)-extractable soil Cd in green areas (4% of total Cd) is lower than in playground soils (58% of total Cd). We attributed the reduced DTPA- and water-extractable Cd, Co, Cr, Mn, and Mo to the formation of stable complexes between metals and OM produced from the continued decomposition of roots of grasses in green spaces.

Conclusions

Grasses accumulate less metal than soils except in roots where Cr and Zn are higher than soils by as much as 31 and 17%, respectively. We conclude that grasses increased (up to 8×) soil OM content in green areas to significantly increase the ability of soils to accumulate nutrients for plants, and to retain and reduce the mobility and toxicity of metals in soils in urban parks.     

Development of Analytical Procedure for the Determination of Exchangeable Cr(VI) in Soils by Anion-exchange Fast Protein Liquid Chromatography with Electrothermal Atomic Absorption Spectrometry Detection

Analytical procedure for the determination of exchangeable Cr(VI) was developed. In order to optimise the extraction procedure, the efficiency of extraction of exchangeable Cr(VI) in soil samples was investigated in KH₂PO₄–K₂HPO₄ buffer solutions (0.015 up to 0.2 mol l^?1), adjusted to the pH of the soil. Phosphate buffer was used to efficiently desorb Cr(VI) from soil particles. The extraction time (mechanical shaking) ranged from 1 up to 72 h. Cr(VI) in soil extracts was determined by anion-exchange fast protein liquid chromatography with electrothermal atomic absorption detection (FPLC-ETAAS). The study was performed on soil samples from the field treated with the tannery waste for seventeen years. Samples were analysed in the 16 year after the last waste application. It was experimentally proven that the optimal phosphate buffer concentration was 0.1 mol l^?1 and extraction time 16 h. An additional experiment was done to confirm that during the extraction, soluble Cr(III) was not oxidised to Cr(VI) by Mn(IV) oxides present in soil samples. For this purpose soil with the same characteristics, but not treated with tannery waste, was spiked with Cr(III) and the analytical procedure performed. No measurable Cr(VI) concentrations were detected. The repeatability of measurement was 2.5%, while the reproducibility of measurement was 6.9%. The accuracy of the analytical procedure was tested by spiking of soil samples with Cr(VI). The recoveries were better than 95%. The analytical procedure with limit of detection (LOD) 15 ng g^?1 of Cr(VI) was sensitive enough for the determination of exchangeable Cr(VI) in soils. In field soil samples analysed the concentrations of exchangeable Cr(VI) were found to be about 200 ng g^?1.     

Predicting phosphorus sorption isotherm parameters in soil using data of routine laboratory tests

Knowledge of phosphorus(P) sorption dynamics across different soil types could direct agronomic and environmental management of P. The objective of this study was to predict P isotherm parameters for a national soil population using data of routine laboratory tests. Langmuir and Freundlich sorption parameters were calculated from two different ranges(0–25 and 0–50 mg P L~(-1)) using an archive of representative agricultural soil types from Ireland.Multiple linear regression(MLR) identified labile forms of aluminium(Al) and iron(Fe), organic matter(OM), cation exchange capacity(CEC), and clay as significant drivers. Langmuir and Freundlich sorption capacities, Freundlich affinity constant, and Langmuir buffer capacity were predicted reliably, with R~2 of independent validation 0.9. Sorption isotherm parameters were predicted from P sorbed at a single concentration of 50 mg P L~(-1)(S_(50)). An MLR prediction of P sorption maximum in the 0–50 mg P L~(-1) range was achieved, to an accurate standard, using S_(50), OM, and Mehlich-3 Fe(R~2 of independent calibration and validation being 0.91 and 0.95, respectively). Using Giles' four shapes of isotherms(C, L, H, and S), L non-strict-and C-shaped isotherm curves accounted for 64% and 27% of the soils, respectively. Hierarchical clustering identified a separation of isotherm curves influenced by two ranges of Mehlich-3 Al. Soils with a low range of Mehlich-3 Al(2.5–698 mg kg~(-1)) had no incidence of rapid sorption(C shape). Single point indices, Al, or available soil data make the regression approach a feasible way of predicting Langmuir parameters that could be included with standard agronomic soil P testing.     

Municipal Solid Waste Compost Improves Crop Productivity in Saline-Sodic Soil: A Multivariate Analysis of Soil Chemical Properties and Yield Response

A pot experiment was conducted in sandy clay loam saline-sodic soil to assess the effects of farm yard manure (FYM), municipal solid waste (MSW) composts and gypsum application on nitrate leaching, soil chemical properties and crop productivity under rice-wheat cropping system. It also aims at establishing the correlation between soil phsico-chemical properties and yield response using principle component analysis and Pearson correlation analysis. The MSW was decomposed aerobically, an-aerobically and co-composted. Maximum nitrate leaching was observed during rice (75.9 mg L^?1) and wheat (37.2 mg L^?1) with an-aerobically decomposed MSW as compared with control treatment. Results revealed a decrease in soil pH (?6.95% and ?8.77%), electrical conductivity (EC) (?48.13% and ?51.04%), calcium carbonate (CaCO₃) (?40.30% and ?48.96%), and sodium adsorption ratio (SAR) (?40.27% and ?45.98%) with an-aerobically decomposed MSW compost during rice and wheat, respectively. In this treatment, organic matter (OM) (93.55% and 121.51%) and cation exchange capacity (CEC) (19.31% and 31.79%) were the highest as compared with control treatment during rice and wheat, respectively. Rice and wheat growth were significantly (p≤ 0.05) increased by an-aerobically decomposed MSW followed by co-compost, aerobically decomposed MSW, FYM, gypsum and control. Furthermore, Pearson correlation coefficients predicted significant positive correlation of yield with soil OM, and CEC while inverse relationship was observed with EC, pH, CaCO₃, and nitrogen use efficiency. Soil amelioration with organic and gypsum amendments was further confirmed with principal component analysis. This study has proved an-aerobically decomposed MSW as an effective solution for MSW disposal, thereby improving soil chemical properties and crop productivity from sandy clay loam saline-sodic soil.     

Unlocking fixed soil phosphorus upon waterlogging can be promoted by increasing soil cation exchange capacity

Phosphorus (P) adsorbed by iron (Fe) oxyhydroxides in soil can be released when the Fe(III) minerals are reductively dissolved after soil flooding. However, this release is limited in tropical soils with large Fe contents and previous studies have suggested that P sorbs or precipitates with newly formed Fe(II) minerals. This hypothesis is tested here by scavenging Fe²⁺ in flooded soils by increasing the cation exchange capacity (CEC) of soil through resin application (30 cmol_c kg^?1; Na‐form). Three soils from rice paddies with contrasting properties were incubated in aerobic and anaerobic conditions with or without resin and with or without addition of organic matter (OM) to stimulate redox reactions. Dissolved Fe was 0.1–1.1 mm in unamended anaerobic soils and decreased to less than 0.07 mm with resin addition. Anaerobic soils without resin and aerobic soils with or without resin had marginal available P concentrations (<2 mg P kg^?1; anion‐exchange membrane P). In contrast, available P increased 3‐ to 14‐fold in anaerobic soils treated with resins, reaching 16 mg P kg^?1 in combination with extra OM. Application of Ca‐forms of resin did not stimulate P availability and dissolved Ca concentrations were larger than in unamended soils. Resin addition can increase P availability, probably by a combination of reducing solution Fe²⁺ (thereby limiting the formation of Fe(II) minerals) and increasing the OM solubility and availability through reducing dissolved Ca²⁺. The soil CEC is a factor controlling the net P release in submerged soils.     

The effect of water movement on the transport of dicyandiamide,ammonium and urea in unsaturated soils

A laboratory experiment was conducted to investigate the relative mobility of dicyandiamide (DCD) and jointly applied ammoniacal salts or urea in three different soils of lower Egypt, and to determine the extent to which DCD separates from N-fertilizer in unsaturated soil undergoing leaching. The experimental results suggest that, under conditions of water flow, DCD is readily separated from NH₄⁺ but parts from urea to a far lesser extent. The large difference in mobility between DCD and NH₄⁺ should severely limit the effectiveness of DCD as a nitrification inhibitor in the three soils considered when applied in conjunction with ammoniacal salts. In two out of three cases, the situation is similarly unfavorable in the case of joint DCD and urea application. However, the observation that DCD, in a low CEC sandy loam, moves within the soil solution at a slightly lower rate than urea suggests that joint application with urea would keep at least part of the DCD in contact with the NH₄⁺ ions and, therefore, would preserve some of the effectiveness of DCD under leaching conditions in this soil.     

褐土区氮磷在土壤发生层中淋溶的差异性

农业氮磷淋溶已经成为地下水污染最普遍和突出的问题。为揭示氮磷在包气带不同土层的淋溶特征,以典型褐土的5个土壤发生层（耕层、淋溶层、钙积层、黏化层和母质层）为研究对象,采用室内土柱模拟淋溶试验,在施肥量相同的条件下分析不同形态氮磷淋溶量,研究氮磷在不同土壤发生层中的迁移特征及其影响因素。结果表明：1）进行5次淋溶,耕层、淋溶层、钙积层、黏化层和母质层淋溶液中可溶性总氮总量分别为2412.63 mg·L^-1、3028.94 mg·L^-1、244.16 mg·L^-1、3648.99 mg·L^-1和3356.51 mg·L^-1,淋溶层、黏化层和母质层可溶性总氮淋溶量显著高于耕层,而钙积层可溶性总氮淋溶量较耕层显著减少;耕层淋溶液中可溶性总磷总量为0.52 mg·L^-1,且显著高于其他4层。2）在试验初期,耕层、淋溶层的硝态氮、可溶性总氮和正磷酸盐淋溶量显著高于黏化层和母质层,进行到第4、5次淋溶,黏化层、母质层的硝态氮和可溶性总氮淋溶量显著高于其他3层,而各发生层间正磷酸盐淋溶量无显著差异;单次淋溶黏化层和母质层铵态氮淋溶量均显著高于其他3层,而耕层可溶性总磷淋溶量始终显著高于其他各层。3）耕层和钙积层的淋溶液中硝态氮是氮素淋溶的主要形态,占可溶性总氮比例分别为69.0%和85.4%,而在淋溶层、黏化层和母质层中分别为41.3%、5.1%和4.6%;在可溶性磷中,以无机态正磷酸盐为主,最高占可溶性总磷的75.9%。4）土壤有机质含量、阳离子交换量、黏粒含量对土壤氮磷的迁移转化有明显主导作用。有机质与氮磷淋溶量呈显著正相关关系,有机质含量高,会增加淋溶初期氮磷的淋溶风险;而阳离子交换量和黏粒含量则与氮磷淋溶呈显著负相关关系,阳离子交换量大和黏粒多能减少氮磷素的淋溶风险。该试验结果说明,由于5种发生层土壤理化性质不同,各发生层氮磷淋溶特征及其淋溶形态也有差异,并且氮磷的淋溶受土壤本身阳离子交换量、黏粒和有机质含量的影响。     

Inorganic and organic ligands induced changes in Pb sorption of arid ‎clay and calcareous loamy sand soils

The objective of this study was to investigate sorption, desorption, and immobilization of Pb in the clay and calcareous loamy sand soils treated with inorganic ligands (NO₃^?, Cl^? and H₂PO₄^?). Pb sorption was also determined in the presence of oxalate and citrate. The maximum Pb sorption capacities (q) ranged from 42.2 to 47.1 mmol kg^?1 for the clay soil, and from 45.2 to 47.0 mmol kg^?1 for loamy sand soil. It was observed that the binding energy constant (k) for Pb sorbed onto loamy sand soil (528–1061) is higher than that for clay soil (24.38–55.29). The loamy sand soil-sorbed greater quantities of Pb compared to the clay soil when initial pH was ≥ 3. However, it had lower sorption capacity at the lowest initial pH of 2. Additionally, the greatest Pb sorption and immobilization occurred in the soil treated with H₂PO₄. In the clay soil, the sorption of Pb was depressed at 0.1 mol kg^?1 of Cl^?, as compared with other ligands. Concerning organic acids, citrate ligand showed the highest decrease in Pb sorption. It could be concluded that the nature of Pb sorption can depend on the type and quantity of ligands present, as well as the soil type.