施用碱稳定固体的酸性土壤的Cu和Zn的形态分布

Fractionation of metals in a granite-derived acid sandy loam soil amended with alkaline-stabilised sewagesIudge biosolids was conducted in order to assess metal bioavailability and environmental mobility soil solution was extracted by a centrifugation and filtration technique. Metal speciation in the soil solution wasdetermined by a cation exchange resin method. Acetic acid and EDTA extracting solutions were used forextraction of metals in soil solid surfaces. Metal distribution in different fractions of soil solid phase was determined using a three-step sequential extraction scheme. The results show that the metals in the soilsolution existed in different fractions with variable lability and metals in the soil solid phase were also presentin various chemical forms with potentially different bioavail ability and environmental mobility Alkaline-stabilised biosolids could elevate solubility of Cu and proportion of Cu in organically complexed fractionsboth in soil liquid and solid phases, and may therefore increase Cu mobility. In contrast, the biosolids lowered the concentrations of water-soluble Zn (labile fraction) and exchangeable Zn and may hence decrease bioavailability and mobility of Zn. However, Fe and Mn oxides bound and organic matter bound fractions are likely to be Zn pools in the sludge-amended soil. These consequences possibly result from the liming effect and metal speciation of the sludge product and the difference in the chemistry between the metals in soil.     

乙炔浓度对厌氧培养的土壤悬浊液反硝化作用及相关的微生物过程的影响

Potentiometric experiments were carried out on the proton binding equilibria of FA extracted from a weathered coal and HA and Fa extracted from a dark loessial soil.The affinity spectrum model was employed to treat the experimental data.The affinity spectrum model technique could“magnify” the heterogeneity of the proton binding equilibria.so it was useful for comparing and studying the characteristics of humic substances with similar properties.According to the affinity spectra,we also found that the direction of the titration could affect the properties of the equilibria of FA from the weathered coal,and the acidic functional groups contained in FA from the weathered coal were larger in quantity than those contained in HA and FA from the dark loessial soil.     

有机物质对土壤溶液中铜形态的影响

Incubation of two soils,a red soil derived from granodiorte and a fluvo-aquic soil from alluvial deposit,with rice straw,Chinese milk vetch and pig manure under submerged condition were conducted to study the species of Cu in soil solutions as affected by the organic materials.The organic materials increased total soluble Cu by raising dissolved organic carbon(DOC) in soil solution when the solution pH values were below the range in which Cu deposited quickly.When the solution pH rose to this rage,the increase of DOC did not raise total soluble Cu.Total soluble Cu in all the treatments dropped with incubation time.After adding organic materials labile Cu dropped with incubation time and decreased sharply in the pH range of Cu precipitation.Addition of organic materials enhanced slowly labile Cu but depressed the ratio of labile Cu to total soluble Cu.Slowly labile Cu decreased with incubation time.Sepwise multiple linear regression analysis showed that total soluble Cu was positively correlated with Eh and DOC(P=0.0025),labile Cu was negatively correlated with pH(P=0.0118),and slowly labile Cu was positively correlated with Eh and DOC(P=0.0022).Both the labile and slowly labile Cu were correlated with total soluble Cu at extremely significant levels.     

草酸对土壤和矿物中钾素的释放规律研究

Oxalic acid plays an important role in improving the bioavailability of soil nutrients. Batch experiments were employed to examine the influences of oxalic acid on extraction and release kinetics of potassium （K） from soils and minerals along with the adsorption and desorption of soil K^＋. The soils and minerals used were three typical Chinese soils, black soil （Mollisol）, red soil （Ultisol）, and calcareous alluvial soil （Entisol）, and four K-bearing minerals, biotite, phlogopite, muscovite, and microcline. The results showed that soil K extracted using 0.2 mol L^-1 oxalic acid was similar to that using 1 mol L^-1 boiling HNO3. The relation between K release （y） and concentrations of oxalic acid （c） could be best described logarithmically as y = a ＋ blogc, while the best-fit kinetic equation of K release was y = a ＋ b√t, where a and b are the constants and t is the elapsed time. The K release for minerals was ranked as biotite 〉 phlogopite 〉〉 muscovite 〉 microcline and for soils it was in the order： black soil 〉 calcareous alluvial soil 〉 red soil. An oxalic acid solution with low pH was able to release more K from weathered minerals and alkaline soils. Oxalic acid decreased the soil K^＋ adsorption and increased the soil K^＋ desorption, the effect of which tended to be greater at lower solution pH, especially in the red soil.     

有机配体、竞争阳离子和pH对土壤中Zn分解的影响

A series of experiments were conducted to examine the interactive effects of an organic ligand, a competing cation, and pH on the dissolution of zinc （Zn） from three California soils, Maymen sandy loam, Merced clay, and Yolo clay loam. The concentrations of soluble Zn of the three soils were low in a background solution of Ca（NO3）2. Citric acid, a common organic ligand found in the rhizosphere, was effective in mobilizing Zn in these soils; its presence enhanced the concentration of Zn in soil solution by citrate forming a complex with Zn. The ability of Zn to form a complex with citric acid in the soil solution was dependent on the concentration of citric acid, pH, and the concentration of the competing cation Ca^2＋. The pH of the soil solution determined the extent of desorption of Zn in solid phase in the presence of citric acid. The amounts of Zn released from the solid phase were proportional to the concentration of citric acid and inversely proportional to the concentration of Ca（NO3）2 background solution, which supplied the competing cation Ca^2＋ for the formation of a complex with citrate. When the soil suspension was spiked with Zn, the adsorption of Zn by the soils was retarded by citric acid via the formation of the soluble Zn-citrate complex. The dissolution of Zn in the presence of citric acid was pH dependent in both adsorption and desorption processes.     

稻田土壤甲烷排放模型: Ⅰ. 模型的建立

With an understanding of the processes of methane production, oxidation and emission, a semi-empirical model, focused on the contributions of rice plants to the processes and also the influence of environmental factors, was developed to predict methane emission from rice paddy soils. In the present model, the amount of methane transported from the soil to the atmosphere was determined by the rates of CH₄ production and an emitted fraction. The rates of CH₄ production in irrigated rice soils were computed from the availability of methanogenic substrates that are primarily derived from rice plants and added organic matter and the influence of soil texture, soil redox potential and temperature. The fraction of methane emitted was assumed to be modulated by the rice plants and declines with rice growth and development. To make it applicable to a wider area with limited data sets, a simplified version of the model was also derived to predict methane emission in a more practical manner.     

化学萃取修复尾渣土壤的金属形态变化特征

The efficiency of EDTA, HNO3 and CaCl2 as extractants to remove Pb, Zn and Cu from tailing soils without varying soil pH was investigated with distributions of Pb, Zn and Cu being determined before and after extraction using the sequential extraction procedure of the optimized European Community Bureau of Reference （BCR）. Results indicated that EDTA and HNO3 were both effective extracting agents.The extractability of extractants for Pb and Zn was in the order EDTA 〉 HNO3 〉 CaCl2, while for Cu it was HNO3 〉 EDTA 〉 CaCl2. After EDTA extraction, the proportion of Pb, Zn and Cu in the four fractions varied greatly, which was related to the strong extraction and complexation ability. Before and after extraction with HNO3 and CaCl2, the percentages of Pb, Zn and Cu in the reducible, oxidizable and residual fractions changed little compared to the acid-extractable fraction. The lability of metal in the soil and the kinds of extractants were the factors controlling the effects of metal extraction.     

阳离子交换膜在土壤钾释放及小麦对钾素的反应研究中的应用

A pot experiment was conducted in the growth chamber on Saskatchewan soils with different texture to determine the K release status and wheat K demand.The relationship between K uptake and soil available K extracted by cation exchange membrane(CEM-K) and the effcet of K fertilizer on wheat growth and soil available K was also evaluated.Treatments of 0,60 and 120mg K/kg were applied to sandy,low and high K loamy and clay soils,The highest yields were acieved with the application of 120mg K/kg in sandy soil and 60 mg K/kg in other soils.On the whole,the clay soil contributed K more than other soils from slowly available fraction.Regression revealed a linear relationship between the soil available K extracted by NH4OAc(Ka) and CEM-K in suspensions(r=0.93).Results also showed that CEM-K in burial and in suspensions were different not only in the amount but also in correlation with Ka or K uptake.     

可溶性有机物对土壤中绿麦隆吸附与解吸的影响

A batch equilibrium techniques was used to examine the effect of dissolved organic matter （DOM） extracted from both non-treated sludge （NTS） and heat-expanded sludge （HES） on the sorption and desorption of chlorotoluron （3-（3-chloro-p-tolyl）-1,1-dimethylurea） in two types of soils, a yellow fluvo-aquic and a red soil from China. Without DOM,sorption of chlorotoluron was significantly greater （P 〈 0.05） in the red soil than in the yellow fluvo-aquic soil. However,with DOM the effect was dependent on the soil type and nature of DOM. Chlorotoluron sorption was lower in the yellow fluvo-aquic soil than in the red soil, suggesting that with the same DOM levels the yellow fluvo-aquic soil had a lower sorption capacity for this herbicide. Application of DOM from both NTS and HES led to a general decrease in sorption to the soils and an increase in desorption from the soils. Desorption of chlorotoluron also significantly increased （P 〈 0.05） with an increase in the DOM concentration. Additionally, for sorption and desorption, at each DOM treatment level the NTS treatments were significantly lower （P 〈 0.05） than the HES treatments. This implied that non-treated sludge had a greater effect on the sorption and desorption of chlorotoluron than heat-expanded sludge.     

作物根系层土壤水分模拟的经验-机理模型

To predict soil water variation in the crop root zone,a general exponential recession (GER) model was developed to depict the recession process of soil water storage.Incorporating the GER model into the mass balance model for soil water,a GER-based physicoempirical (PE-GER) model was proposed for simulating soil water variation in the crop root zone.The PE-GER model was calibrated and validated with experimental data of winter wheat in North China.Simulation results agreed well with the field experiment results,as well as were consistent with the simulation results from a more thoroughly developed soil water balance model which required more detailed parameters and inputs.Compared with a previously developed simple exponential recession (SER) based physicoempirical (PE-SER) model,PE-GER was more suitable for application in a broad range of soil texture,from light soil to heavy soil.Practical application of PE-GER showed that PE-GER could provide a convenient way to simulate and predict the variation of soil water storage in the crop root zone,especially in case of insufficient data for conceptual or hydrodynamic models.     

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.     

Zinc Desorption of Calcareous Soils as Influenced by Applied Zinc and Phosphorus and Described by Eight Kinetic Models

The activity of zinc (Zn) ions in the soil solution bathing plant roots is controlled by the simultaneous equilibrium of several competing reactions, such as surface exchange, specific bonding, lattice penetration, precipitation reactions, and the processes leading to the desorption of surface and lattice-bound ions. Desorption of Zn in 15 calcareous soils from southern Iran, treated with 10 mg Zn kg^?1 soil as zinc sulfate (ZnSO₄·7H₂O) and 100 mg phosphorus (P) kg^?1 soil as calcium phosphate [Ca(H₂PO₄)₂H₂O] and then equilibrated and extracted with diethylentriaminepentaacetic acid (DTPA), was studied in this experiment. The results were fitted to zero-order, first-order, second-order, third-order, parabolic diffusion, two-constant rate, Elovich, and simple Elovich kinetic models. Two-constant rate, simple Elovich, and parabolic diffusion models were determined to best describe Zn-desorption kinetics. Zinc desorption increased as Zn was applied but decreased with applied P.     

Phosphorus desorption and isotope exchange kinetics in agricultural soils

To improve phosphorus (P) fertilization and environmental assessments, a better understanding of release kinetics of solid-phase P to soil solution is needed. In this study, Fe (hydr)oxide-coated filter papers (Fh papers), isotopic exchange kinetics (IEK) and chemical extractions were used to assess the sizes of fast and slowly desorbing P pools in the soils of six long-term Swedish field experiments. The P desorption data from the Fh-paper extraction of soil (20 days of continual P removal) were fitted with the Lookman two-compartment desorption model, which estimates the pools of fast (Q₁) and slowly (Q₂) desorbing P, and their desorption rates k₁ and k₂. The amounts of isotope-exchangeable P (E) were calculated (E_1min to E_{>3 months}) and compared with Q₁ and Q₂. The strongest relationship was found between E_{1 min} and Q₁ (r² = .87, p < .01). There was also an inverse relationship between the IEK parameter n (the rate of exchange) and k₁ (r² = .52, p < .01) and k₂ (r² = .52, p < .01), suggesting that a soil with a high value of n desorbs less P per time unit. The relationships between these results show that they deliver similar information, but both methods are hard to implement in routine analysis. However, Olsen-extractable P was similar in magnitude to Q₁ (P-Olsen = 1.1 × Q₁ + 2.3, r² = .96), n and k₁ were related to P-Olsen/P-CaCl₂, while k₂ was related to P-oxalate/P-Olsen. Therefore, these extractions can be used to estimate the sizes and desorption rates of the different P pools, which could be important for assessments of plant availability and leaching.     

Time‐dependent zinc desorption in soils

Abstract

Time dependent zinc (Zn) desorption in eight benchmark soils of India was studied in relation to various pH values and ionic strengths. Soil samples were equilibrated in solutions containing 10 μg Zn g^‐1 soil at pH 5.5,6.5, and 7.5 for 48 h at 25±2°C, and adsorbed Zn extracted with calcium chloride (CaCl₂) for various periods of time. Desorption of Zn decreased with increasing pH, and the desorption rate decreased abruptly at pH 7.5. In contrast, an increase in the equilibration period and ionic strength of the background electrolyte increased Zn desorption. Four rival kinetic models were fitted and evaluated for their suitability for describing the Zn desorption process. Reaction rate constant (ß) calculated from the Elovich model for the different soils ranged from 9.99 to 25 (mg Zn kg^‐1)^‐1. The different kinetic models tested indicated that Zn desorption in soils was a diffusion controlled process. The desorption was rapid in the first 4 h, followed by slower phase in the rest of the time at all the pH values indicating a biphasic desorption, characteristic of a diffusion controlled process. The ß value for the Elovich equation showed a strong association with soil clay content and cation exchange capacity (CEC). Further, the best prediction of Zn desorption reaction rate constant could be made using multiple‐regression equation with soil clay content and CEC as variables.     

Kinetics of Copper Desorption from Highly Calcareous Soils

Abstract

Desorption of copper (Cu) is an important factor in determining Cu availability in calcareous soils. Kinetics of native and added Cu desorption by DTPA (diethylene‐triaminepentaacetic‐acid) from 15 highly calcareous soils of southern Iran were studied in a laboratory experiment. Our results showed that two constant‐rate, Elovich, simple Elovich, and parabolic‐diffusion equations were the best‐fitted equations among eight kinetic models used. The copper desorption pattern based on the parabolic‐diffusion equation revealed that the rate of native Cu desorption was higher in the first 2 h followed by a slower release rate, which suggests that two different mechanisms are involved. The trend may describe why the DTPA soil test has been considerably successful in predicting Cu availability in calcareous soils. Stepwise multiple regression equations indicated that CCE (calcium carbonate equivalent), CEC (cation exchange capacity), and clay content are the most important soil characteristics that predict the rate constants of the kinetic models. Mean extractant recovery percentage (ERP) of the soils was only 20%, which indicated that after 20 days, DTPA extracted only one‐fifth of added Cu. Regression equations indicated that as soil OM (organic matter) content increased, the value of ERP decreased. From results reported herein it seems that CCE, CEC, and clay are the most important factors controlling Cu release from highly calcareous soils of southern Iran. However, the initial soil Cu desorption rate is probably controlled by CEC.     

Labile pools of copper and zinc in calcareous soils as measured by DTPA and plant extraction

Abstract

Labile pools of Cu and Zn were measured on two calcareous soils from Saudi Arabia, using successive extraction with DTPA, and successive cropping followed by extraction with DTPA after cropping. The examined soils differed in their ability to supply Cu and Zn. The first DTPA extraction removed a major proportion of the labile pool, particularly in the sandy soil. The two soils showed a general decrease in extractable Cu and Zn with progressive extractions, with DTPA extractable Cu declining more rapidly than Zn. DTPA extractable Cu and Zn determined after cropping were highly correlated with DTPA extractable Cu and Zn values obtained after successive extractions. The results gave evidence on both the contribution of element dissolution from insoluble forms with progressive extraction or cropping, and the usefulness of the DTPA extractant for monitoring the availability of Cu and Zn in these calcareous soils.     

Depletion of soil phosphorus as assessed by several indices of phosphorus supplying power

This study attempts to clarify the advantages and shortcomings of various laboratory tests that are used to characterize the status and dynamics of soil phosphorus (P). We analysed a set of soil samples differing in P status for inorganic P fractions, water‐soluble P (Pw60) and bicarbonate‐extractable P (P_Olsen) both before and after a pot experiment in which soil was depleted. Their P exchange characteristics were determined by Q/I plots, fitted by a modified Langmuir equation, and the supplying power was further assessed by extracting soil samples with various amounts of water. The sensitivity of the P tests in assessing the decrease in inorganic reserves of P was expressed using a response index that was defined as the ratio between the decrease in inorganic P and the decrease in soil P test value. For P_Olsen, the index ranged from 6 to 11 and for Pw60 from 10 to 26. Desorption curves obtained by extracting soil samples with different amounts of water indicate increased buffering power and that large reserves of P were released from soil in weak solutions (P < 0.030 mg l^?1) around soil particles. Although the constants of the Langmuir equation responded reasonably well to the changes in reserves of P in the soil, the results suggest caution is needed in the quantitative interpretation of the constant Q₀ (instantly labile P) of the Langmuir equation.     

Influence of residual phosphate fertilizer on labile and extractable zinc in hawaii soils

Abstract

Zinc availability was studied using five soils from Hawaii which had histories of massive phosphorus applications. Heavy phosphate fertilization usually increased extractable Zn, irrespective of the extractant used. The extra extractable Zn associated with the added P probably came from Zn as an accessory element in the fertilizer. Treble superphosphate commonly used in Hawaii contains about 1400 ppm Zn. The Zn content of phosphate fertilizers must be considered before making statements about the effect of fertilizer P on Zn solubility and availability in soils.

Two solutions (0.1N HCl and 0.005M DTPA) were compared as Zn extractants for Hawaii soils. DTPA extracted less Zn than 0.1N HCl. Zinc extracted by repeated HCl treatment was more closely related to the labile Zn pool (E‐values and L‐values) than was DTPA‐extractable Zn. The results suggest that 0.1N HCl extractable Zn, Zn E‐value and Zn L‐value measured the quantity of a single fraction of soil Zn.

Repeated extraction of soil with 0.1N HCl seems to be a suitable procedure for evaluating the Zn status of acid, highly weathered soils of Hawaii.     

Comparisons of Various Chemical Extracts as Quantity Factors to Determine Metal-Buffering Capacity of Soils

Applicability of various chemical extracts was investigated as quantity (Q) factors to determine cadmium (Cd), zinc (Zn), and copper (Cu) desorption quantity–intensity (Q/I) relationships in soils. The metal extracts were sums of sequential metal fractions (except the residual fraction) using Tessier's (TSE) and Community Bureau of Reference (BCR) procedures and various single chemical extracts: 1.0 M potassium nitrate (KNO₃), 1.0 M magnesium nitrate [Mg(NO₃)₂], 1.0 M magnesium chloride (MgCl₂), and 0.11 M acetic acid (CH₃COOH) solutions. Water-extractable metal was applied as a fixed intensity (I) factor. The TSE or BCR metal fractions were significantly correlated with diethylenetriaminepentaacetic acid (DTPA)–extractable metals, and all the metal desorption Q/I curves were linearly fitted. However, most of metal BC values estimated by using the single chemical extracts were very low and did not have consistent trends for target metals. Only 0.11 M CH₃COOH-extractable metals might be reliable. Therefore, TSE and BCR metal fractions can be applicable to replace DTPA-extractable metals, and 0.11 M CH₃COOH-extractable metals might also be useful.     

Effect of wheat (Triticum aestivum L.) rhizosphere and sewage sludge application on zinc desorption with dilute citric acid

Rhizosphere processes have a major impact on Zn desorption and Zn uptake by plant. However, information about Zn desorption characteristics in the rhizosphere of wheat is limited. Therefore, a greenhouse experiment was performed to determine Zn desorption characteristics in the bulk and rhizosphere soil of wheat (Triticum aestivum L.) of 10 soils amended and un-amended with municipal sewage sludge using rhizoboxes. The kinetics of Zn desorption was determined by successive extraction with 10 mM citric acid in a period of 1–504 h at 25 ± 1°C in the bulk and rhizosphere of un-amended and amended soils. The results showed that the Zn amount extracted after 504 h in the rhizosphere soils was significantly (p < 0.01) higher than the bulk soils. The mean of Zn desorption in the bulk and rhizosphere of un-amended soils were 10.4 ± 0.34 and 11.4 ± 0.43 mg kg^?1, respectively, while the mean of Zn desorption in the bulk and the rhizosphere of amended soils were 13.2 ± 0.48 and 14.8 ± 0.67 mg kg^?1, respectively. Desorption kinetics of Zn conformed fairly well to the first-order, parabolic diffusion, power function, and zero-order equations. The results of Zn fractionation indicated that exchangeable Zn and Zn associated with organic matter decreased and Zn associated with iron-manganese oxides and residual Zn increased in the rhizosphere soils compared to the bulk soils. Zinc desorption after 504 h and residual Zn in the bulk and rhizosphere of un-amended and amended soils were significantly positively correlated (p < 0.05). Therefore, residual Zn was the main Zn pool that controlled Zn desorption after 504 h in the bulk and rhizosphere soils studied.