Stability behavior of soil colloidal suspensions in relation to sequential reduction of soils

The cause of the decrease in the Fe²⁺ concentration of the soil solution in the later period of soil waterlogging was investigated. After 7-d incubation of the soil solutions separated from previously waterlogged soils (PWdS), a greyish precipitate (PPT) was observed in the soil solutions. The color of the PPT became reddish brown after separation from the solutions and freeze-drying. The PPT observed in 14-d-PWdS contained 352.6 g Fe kg^-1, 62.5 g C kg^-1, 22.6 g P kg^-1, 11.3 g Si kg^-1, 9.9 g N kg^-1, 0.7 g Al kg^-1 and a trace amount of Mn. However, Ca, Mg, K, and Na could not be detected. It was concluded that the separated PPT was dominated by amorphous ferric hydroxide based on the chemical analysis, broad IR absorption band at 585 cm^-1 and exothermic peak at 301°C. The data of chemical analysis and the characteristic IR bands of the PPT suggested that organic substances and presumably aluminosilicate anion were adsorbed onto the freshly-formed ferric hydroxide. The dominant phase of the greyish PPT in the reductive soil solution was considered to be ferrous PPT and was assumed to consist mainly of carbonate and/or hydroxide, and concomitantly of phosphate. The formation of the ferrous PPT in the soil solution in the later period of soil waterlogging was considered to (i) cause the decrease of concentration of Fe²⁺ ion and of other divalent cations such as Ca²⁺ due to the re-adsorption of Ca²⁺ on soil clays through the cation exchange reaction with Fe²⁺ ion, and consequently (ii) enhance the dispersion of the soil colloidal suspension.     

Transport and deposition of dilute colloidal suspensions in soils

Transport and deposition of suspended particles occur during many soil processes. The mechanisms of removal of particles from suspension during saturated flow are described, and a simple equation of depth filtration is used to test experimental data. A method for labelling dilute clay suspensions with ¹⁴C-paraquat is developed. Particles are removed from flowing suspension even when they are dispersed. The depth filtration equation holds only under these conditions, though the mechanisms of removal of particles from suspension by the soil are unclear. A surprisingly large reduction in flow rate accompanies passage of dilute clay suspensions through soil columns.     

Stability of soil aggregates in relation to organic constituents and soil water content

The effects of soil organic matter content, soil water content and duration of wet-sieving on aggregate stability of soils with contrasting cropping histories were investigated. Long-term pasture samples had a greater aggregate stability than long-term arable samples. However, air-drying aggregates before wet-sieving increased the aggregate stability of long-term pasture samples, but decreased that of long-term arable samples. With increasing duration of wet-sieving, the proportion of water-stable aggregates declined until a near-constant value was reached for each sample. Thus, within a sample there are aggregates possessing a wide range of stabilities; with increasing time under arable cropping there is an increase in the proportion of unstable aggregates present, and the measured aggregate stability, therefore, declines. Unstable aggregates (defined as those dispersed after wet-sieving for 1 min) generally had lower organic matter content than stable ones (those still intact after sieving for 15 min). The aggregate stability of a regrassed site (13 years of arable plus 2 years of pasture) was markedly higher than that of a corresponding site from 15 years of arable cropping. Nonetheless, levels of organic matter (organic C, total N and hydrolysable carbohydrate) were almost identical at the two sites. However, aggregates from the regrassed site did have a higher biomass C and water-extractable carbohydrate content than those from the 15-year arable site. For a group of soils with varying cropping histories, aggregate stability was significantly more closely correlated with hot water-extractable carbohydrate content than with organic C or hydrolysable carbohydrate content. It is suggested that the hot water-extractable carbohydrate fraction may represent a pool of carbohydrate involved in the formation of stable aggregates.     

Micronutrients distribution in salt-affected soils of the Punjab in relation to soil properties

Salt-affected soils in arid and semi-arid tracts of the Indian Punjab are prone to deficiency of micronutrients. Nine profiles from alluvial terraces, sand dunes and palaeochannels in the southwestern Punjab were investigated for total and diethylenetriamine-penta-acetic acid (DTPA) extractable Zn, Cu, Mn and Fe. Soil physiography exerted significant influence on the spatial distribution of micronutrients. Total contents varied from 20–78 for Zn, 8–32 for Cu, and 88–466 mg kg^?1 for Mn and 0.82–2.53% for Fe. DTPA-extractable contents varied from 0.10–0.98 for Zn, 0.14–1.02 for Cu, 0.54–13.02 for Fe and 0.82–9.4 mg kg^?1 for Mn. Total contents were higher in fine-textured soil than in coarse-textured soils. Concentration of micronutrients in the surface layer was low and there occurred more accumulation in the Cambic horizon. Organic carbon, pH, clay, silt and calcium carbonate exerted strong influence on the distribution of micronutrients. DTPA extractable Zn, Cu, Mn and Fe increased with increasing organic carbon but decreased with increase in pH and calcium carbonate content. Total micronutrient contents increased with increase in clay, silt and calcium carbonate contents and decreased with increase in sand content.     

Boron adsorption characteristics of some acidic alluvial soils in relation to soil properties

Abstract

We investigated boron (B) adsorption characteristics for 16 acid alluvial soils as a function of equilibrium B concentration (0–80 μg/mL) and the effect of soil properties on such adsorption. The adsorption data for the soils could be described by Freundlich, Temkin, and BET isotherm equations over the entire concentration ranges studied, and by Langmuir and Eadie‐Hofstee equations only over a limited range. In general, the B adsorption capacity and the energy of retention of the soils calculated from different equations are low, the average Langmuir adsorption maxima and bonding energy constant being 21.47 μg/g and 0.113 mL/μg, respectively, making B susceptible to leaching losses. Simple and multiple regression analysis show that the adsorption capacities are significantly influenced by organic carbon (C), cation exchange capacity (CEC), and different forms of aluminium (Al) content in soils. The energy related constants are also influenced by the forms of Al in soils. Existence of significant correlations between constants obtained from different equations confirmed the adsorption characteristics of the soils.     

Carbon stocks in Ethiopian soils in relation to land use and soil management

The effect of soil management and land use change are of interest to the sustainable land management for improving the environment and advancing food security in developing countries. Both anthropogenic changes and natural processes affect agriculture primarily by altering soil quality. This paper reviews and synthesizes the available literatures related to the influence of soil management and land use changes on soil carbon (C) stock in Ethiopia. The review shows that topsoil C stock declines approximately 0–63%, 0–23%, and 17–83% upon land use conversion from forest to crop land, to open grazing, and to plantation, respectively. An increase of 1–3% in soil C stock was observed within 10 years of converting open grazed land to protected enclosures. However, there was a little change in soil C stock below 20 cm depth. There is a large potential of increasing SOC pool with adoption of land restorative measures. Total potential of soil C sequestration with the adoption of restoration measures ranges 0·066–2·2 Tg C y⁻¹ on rain‐fed cropland and 4·2–10·5 Tg C y⁻¹ on rangeland. Given large area and diverse ecological conditions in Ethiopia, research data available in published literature are rather scanty. Therefore, researchable priorities identified in this review are important. Copyright © 2008 John Wiley & Sons, Ltd.     

Sterols in soil organic matter in relation to nitrogen mineralization in sandy arable soils

Unusually low net N mineralization in soils relatively rich in total organic C and N was repeatedly reported for sandy arable soils in NW Europe. In order to adequately account for it in simulation models, it is necessary to know the involved substances and processes. Therefore, 9 arable top soils (< 6% clay) with a wide range of total organic C (1.1%–5.2%) and C : N ratios (12–35) were studied. The soils varied strongly in the mineralizability of soil organic N which was determined via long‐term laboratory incubations (> 200 d). It was hypothesized that mineralization was controlled by antioxidants, and the Trolox equivalent antioxidant capacity (TEAC) of the soils was measured. In addition, pyrolysis–field ionization mass spectrometry (Py‐FIMS) was applied to investigate the influence of the molecular‐chemical composition of soil organic matter. In these soils, the compound class of sterols from Py‐FIMS analysis was most closely, negatively correlated with the mineralizability of soil organic N (r² = 0.75, p = 0.003). This was probably not an antioxidative effect, because the TEAC values did not correlate sufficiently with the mineralizability and the sterol intensities. However, the negative relation with sterols could be causal, since the correlation was about as close with other components of the compound class of sterols and even closer with the main plant sterol beta‐sitosterol (r² = 0.84, p = 0.001). In addition, the variability among samples was strongly governed by the proportions of sterols, and sterols also had a high discriminating power in discriminant analysis. Furthermore, the proportions of sterols were extraordinary in those arable podzol soils that developed under previous heath‐ or woodland (up to 10.2% of total ion intensity from Py‐FIMS). In conclusion, the inhibitory effect of these compounds needs to be investigated in more detail in order to optimize parameterization of N as well as C simulation models especially for podzolized, sandy arable soils with former heath‐ or woodland vegetation.     

An approach for the critical coagulation concentration estimation of polydisperse colloidal suspensions of soil and humus

Purpose

The critical coagulation concentration (CCC) is considered as one of the most important parameters to evaluate the particles aggregation and sedimentation behaviors in the environment. Even though there are a few methods for its measurement, each method has its limitations especially as those methods to be applied to polydisperse systems like soil. Thus, the purpose of this research is to establish a new and more reliable method for its determination.

Materials and methods

Two types of polydisperse colloidal materials were adopted: soil and humus in the experimental studies. The dynamic light scattering technique was employed to determine the effective hydrodynamic diameter of the particles or aggregates changing with time under different pH and electrolyte concentrations of CaCl₂ or KCl. In addition, the fractal dimension of aggregates was also detected with the static light scattering technique.

Results and discussion

A new aggregation rate total average aggregation rate (TAA rate) was defined firstly. We found the defined TAA rate increased linearly with the increase of electrolyte concentration at electrolyte concentrations lower than the CCC value, and the TAA rate stayed approximately constant at electrolyte concentrations higher than the CCC value; an intersection point of the two straight lines therefore could be observed, and the electrolyte concentration at the intersection point will theoretically be the CCC value. The experimental results for the two materials under different pH conditions indeed meet those theoretical predictions, which imply that the CCC value can be determined through the measurement of the TAA rate under different electrolyte concentrations. The comparison of the CCC values obtained between our new method and the widely applied stability ratio method showed that the new method was much better than the stability ratio method for the two polydisperse materials. In addition, the static light scattering measurements also showed that the variations of the fractal dimensions of the aggregates with electrolyte concentrations could be well explained by the CCC values obtained by the new method, which once again verified the applicability of the new method.

Conclusions

A new theory and a corresponding new method for the CCC estimation, which can be applied to polydisperse colloidal suspensions, were developed, and the new method has been demonstrated to be much better than the widely applied method for polydisperse materials in environment.     

Assessment of a sequential extraction procedure for fractionation of soil arsenic in contaminated soils

A sequential fractionation scheme, based on a soil phosphorous fractionation, was developed to assess the chemical nature, and thus the potential bioavailability and mobility of As, at the sites. Soil As was separated into five fractions with (i) anion exchange resin, (ii) NaHCO₃, (iii) NaOH, (iv) HCl, (v) residual. Most sites contained relatively low concentrations of As in the two most labile fractions. The bulk of the contaminant As at the sites seemed to be associated with soil amorphous Fe and Al minerals and the dominant clay minerals which help in As sorption are montmorillonite and mica. Resin-extractable As in particular might provide a good index of potential As bioavailability and mobility.     

Potassium fertilization on sandy soils in relation to soil test,crop yield and K-leaching

To study the influence of potassium (K) fertilizer rate on soil test K values, crop yield, and K-leaching in sandy soils, four long-term fertilizer experiments (0–60–120–180 kg K ha^?1 a^?1) were initiated in 1988 in northern Germany on farmers fields. Clay content of the plow layer was about 4%, and organic matter between 2% and 5%. Plant available soil K was estimated with the double lactate (DL) method. Small grain cereals (rye and barley) did not respond to K fertilization in the 7-year period even though the soil test value of the K-0 plots decreased from ca. 90 to ca. 30 mg K_DL kg^?1 within 3 years. This value remained almost constant thereafter. Crop removal (including straw) of 75 kg K ha^?1 a^?1 was therefore apparently supplied from nonexchangeable K fractions. Compared to the optimum, no K application reduced the yield of potato by up to 21%, and that of white sugar yield up to 10%. Maximum potato yield was obtained by annually applying 60 kg K ha^?1 which resulted in a test value of 60 mg K_DL kg^?1 soil. Maximum potato yield was also obtained at 40 mg K_DL kg^?1 soil, however, with a single application of 200 kg K ha^?1. Similar results were obtained with sugar beet. This indicates that for maximum yield, even for K demanding crops, it is not necessary to maintain K_DL values above 40 mg K kg^?1 soil throughout the entire crop rotation. Soil test values increased roughly proportional to the K fertilizer level. About 120 kg fertilizer K ha^?1 a^?1, markedly more than crop K removal, was required to maintain the initial K_DL of 90 mg kg^?1. The K concentration of the soil solution in the top soil measured after harvest was increased exponentially by K fertilizer level and so was K leaching from the plow layer into the rooted subsoil. The leached quantity increased from 22 kg K ha_?1 a_?1 in the plot without K application to 42.79 and 133 kg Kha^?1 a^?1 in plots supplied with 60, 120 and 180 kg K ha^?1 a^?1 respectively. Soil test values around 100 mg K_DL kg^?1 on sandy soils, as often found in the plow layer of farmers fields, lead to K leaching below the root zone that may exceed the critical K concentration of 12 mg K T^?1 for drinking water.     

基于非线性特征的黏弹性悬架系统减振特性分析

为分析履带式工程车辆黏弹性悬架系统的非线性阻尼减振特性,根据其结构特点和非线性特征,建立该系统两自由度分段非线性振动模型,并由平均法推导出系统固有频率共振区附近的幅频特性方程。以装有黏弹性悬架的某300kW履式拖拉机为应用对象进行研究,分析系统在固有频率共振区附近的非线性特性和阻尼减振性能。讨论了激励幅值、地面刚度、悬架分段非线性刚度、分段线性阻尼系数、车体质量和幅频特性之间的关系,并提出改善系统减振性能的建议。该文的理论与分析方法,可为黏弹性悬架参数与系统减振性能的一致性优化设计提供参考。     

土壤磷有效性及其与土壤性质关系的研究

选取我国14个不同地点土样,测定理化性质、全磷、速效磷、水溶性磷含量,采用通径分析研究土壤磷有效性与土壤性质的关系。结果表明,土壤磷有效性是各个土壤性质综合作用的结果。土壤CEC、有机碳、粘粒、砂粒、碳酸钙含量对土壤速效磷比例影响显著,土壤CEC、粘粒、砂粒含量对土壤速效磷比例贡献为正值,而土壤有机碳对土壤速效磷比例贡献为负值;土壤pH和CEC含量对土壤水溶性磷含量影响显著,土壤pH对水溶性磷比例贡献为正值,土壤CEC对土壤水溶性磷比例贡献为负值。本文所选土样基本符合土壤磷有效性与土壤性质之间通径分析的结果。     

从土壤悬浮液的Wien效应推断阳离子与电渗析粘粒组分的相互作用

The electrical conductivities (ECs) of suspensions containing 25 and 30 g kg-1 solids prepared from theelectrodialyzed clay fraction (＜ 2 μm in diameter) of latosol, yellow-brown soil, and black soil, dispersed invarious nitrate solutions having concentrations of 1 × 10-4/z mol L-1, where z is the valence, and in distilledwater, were measured at field strengths ranging from 14 kV cm-1 to 210 kV cm-1. On the basis of analysesof the charge density and exchangeable ion composition on the surfaces of soil particles in the suspensions,and of the characters of the EC-field strength curves of the various suspensions, it was inferred that theincrement of EC (△EC) and/or relative electrical conductivity (REC) can indicate the bonding strengthbetween cations and soil particles. The bonding strengths of various cations with the soils diminished in theorder: K+ ＞ Zn2+ ＞ Mg2+ ＝ Ca2+ ＞ Na+ for latosol, Ca2+ ＞ Zn2+ ＞ Mg2+ ＝ K+ ＞ Na+ for yellow-brownsoil, and Zn2+ ＞Ca2+ ＞ Mg2+ ＞ K+ ＞ Na+ for black soil.     

Net sulfur mineralization potential in Swedish arable soils in relation to long-term treatment history and soil properties

The long-term treatment effect (since 1957–1966) of farmyard manure (FYM) application compared with crop residue incorporation was investigated in five soils (sandy loam to silty clay) with regards to the net sulfur (S) mineralization potential. An open incubation technique was used to determine accumulated net S mineralization (S_AccMin) and a number of soil physical and chemical properties were determined. Treatments and soil differences in S_AccMin, as well as correlations with soil variables, were tested with single and multivariate analyses. Long-term FYM application resulted in a significantly (p = 0.012) higher net S mineralization potential, although total amounts of C, N, and S were not significantly (p < 0.05) increased. The accumulated S mineralization differed significantly (p < 0.05) between soils within this treatment. The measured soil variables were not significantly correlated to S_AccMin. Conclusively, different treatment histories influenced the quality (e.g., chemical composition) and cycling rate of the organic S pool, rather than its size.     

Decomposition rates and feeding activities of soil fauna in deciduous forest soils in relation to soil chemical parameters following liming and fertilization

 This study investigated the influence of liming and P/K fertilization on the feeding activities of soil fauna and leaf litter decomposition rates in deciduous forest soils. The parameters examined were correlated to soil chemical characteristics. In 1994, we established a field experiment with six plots in an oak-beech forest and added different amounts of dolomite, partly combined with P/K fertilization. Two years thereafter a bait-lamina test was used to examine the feeding activity of soil fauna and a minicontainer test to study beech-leaf decomposition. In 1996, the feeding activity in the Ah horizon was lower in the plots left untreated in 1994 than in the plots which had been fertilized in 1994. The highest feeding activity was found in the treatment with 6 t dolomite ha^–1 plus P/K. In all plots, the feeding activity decreased with increasing soil depth. The decomposition rates varied from 0.49% to 0.78% week^–1 in the period April–October 1996. In 1996, the plots treated with 6 t dolomite ha^–1 had the highest decomposition rates and differed significantly from those treated with 9 t or 15 t dolomite ha^–1. No significant differences were found between the untreated plots and those treated with 9 t or 15 t dolomite ha^–1. These results were confirmed by those obtained in 1997. The C/N ratio of litter also decreased, mostly in the treatment with 6 t dolomite ha^–1. Feeding activities in the Ah horizon correlated positively with pH and concentrations of mobile Ca, Mg, K, and negatively with concentrations of mobile Al and heavy metals. We concluded that an increased supply of mobile nutrients and a decrease in mobile Al and heavy metals in these forest soils, as well as a balanced ratio between macro- and micronutrients, led to increased biological activity. Received: 26 June 1998     

Nitrogen mineralization in relation to site history and soil properties for a range of Australian forest soils

Rates of N mineralization were measured in 27 forest soils encompassing a wide range of forest types and management treatments in south-east Australia. Undisturbed soil columns were incubated at 20°C for 68 days at near field-capacity water content, and N mineralization was measured in 5-cm depth increments to 30 cm. The soils represented three primary profile forms: gradational, uniform and duplex. They were sampled beneath mature native Eucalyptus sp. forest and from plantations of Pinus radiata of varying age (<1 to 37 years). Several sites had been fertilized, irrigated, or intercropped with lupins. The soils ranged greatly in total soil N concentrations, C:N ratios, total P, and sand, silt, and clay contents. Net N mineralization for individual soil profiles (0–30 cm depth) varied from 2.0 to 66.6 kg ha^-1 over 68 days, with soils from individual depths mineralizing from <0 (immobilization) to 19.3 kg ha^-1 per 5 cm soil depth. Only 0.1–3.1% of the total N present at 0–30 cm in depth was mineralized during the incubation, and both the amount and the percentage of total N mineralized decreased with increasing soil depth. N fertilization, addition of slash residues, or intercropping with lupins in the years prior to sampling increased N mineralization. Several years of irrigation of a sandy soil reduced levels of total N and C, and lowered rates of N mineralization. Considuring all soil depths, the simple linear correlations between soil parameters (C, N, P, C:N, C:P, N:P, coarse sand, fine sand, silt, clay) and N mineralization rates were generally low (r<0.53), but these improved for total N (r=0.82) and organic C (r=0.79) when the soils were grouped into primary profile forms. Prediction of field N-mineralization rates was complicated by the poor correlations between soil properties and N mineralization, and temporal changes in the pools of labile organic-N substrates in the field.     

Microbial and soil parameters in relation to N mineralization in soils of diverse genesis under differing management systems

 Oregon soils from various management and genetic histories were used in a greenhouse study to determine the relationships between soil chemical and biological parameters and the uptake of soil mineralized nitrogen (N) by ryegrass (Lolium perenne L.). The soils were tested for asparaginase, amidase, urease, β-glucosidase, and dipeptidase activities and fluorescein diacetate hydrolysis. Microbial biomass carbon (C) and N as well as metabolic diversity using Biolog GN plates were measured, as were total soil N and C, pH, and absorbance of soil extracts at 270 nm and 210 nm. Potentially mineralizable N (N₀) and the mineralization rate constant (k) were calculated using a first order nonlinear regression model and these coefficients were used to calculate the initial potential rate of N mineralization (N₀ k). Except for Biolog GN plates, the other parameters were highly correlated to mineralized N uptake and each other. A model using total soil N and β-glucosidase as parameters provided the best predictor of mineralized N uptake by ryegrass (R ² =0.83). Chemical and biological parameters of soils with the same history of formation but under different management systems differed significantly from each other in most cases. The calculated values of the initial potential rate of mineralization in some cases revealed management differences within the same soil types. The results showed that management of soils is readily reflected in certain soil chemical and biological indicators and that some biological tests may be useful in predicting N mineralization in soils. Received: 31 January 1997     

Adsorption of chloride and nitrate by variable charge soils in relation to the electric charge of the soil

A cell consisting of a chloride-selective electrode and a nitrate-selective electrode was directly put in the soil suspension to determine the concentration ratio NO₃^?/Cl^? for studying the adsorption of these two ions by three soil samples from variable charge soils. It was found that such factors as the iron oxide content of the soil, the pH of the suspension, the concentration of the respective anion, the kind of accompanying cations, and the dielectric constant of solvent etc. can all affect the amounts and the ratio of the two anions adsorbed. The adsorption was chiefly caused by coulombic force, but another mechanism, presumably a covalent force between the anion and the metal atom on the surface of soil particles, may also be involved, at least for chloride ions.