伊朗西部地区碱性土壤中共离子对Zn吸附的影响

Zinc(Zn) is essential to plant growth and relatively mobile in soils.This study was conducted to assess the effect of common ions(Ca 2+,K +,Na +,NH + 4,Cl,NO 3,and H 2 PO 4) on sorption of Zn in surface samples of ten calcareous soils from western Iran using 10 mmol L 1 KCl,KNO 3,KH 2 PO 4,Ca(NO 3) 2,NaNO 3,and NH 4 NO 3 solutions as background electrolytes.The results indicated that both NH + 4,K +,and Ca 2+ equally decreased Zn sorption as compared to Na +.Zinc sorption was decreased by H 2 PO 4 as compared to NO 3 and Cl.The Langmuir and Freundlich equations fitted closely to the sorption data of all ions.The Langmuir maximum,bonding energy constant,and Freundlich distribution coefficient for Zn sorption differed among the various ionic background electrolytes.Langmuir sorption parameters showed that the presence of H 2 PO 4 decreased the maximum Zn adsorbed,but increased the bonding energy.Although K + and NH + 4 equally influenced maximum Zn adsorbed,they differed in their effect on the distribution coefficient of Zn in soils.Values of saturation index calculated using Visual MINTEQ indicated that at the low Zn concentration,Zn solubility was controlled by sorption reactions and at the high Zn concentration,it was mainly controlled by sorption and mineral precipitation reactions,such as precipitation of Zn 3(PO 4) 2.4H 2 O,Zn 5(OH) 6(CO 3) 2,and ZnCO 3.For most ionic background electrolytes,soil pH,CaCO 3,and cation exchange capacity(CEC) were significantly correlated with sorption parameters.     

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.     

Factors affecting potassium fixation in calcareous soils of southern Iran

Potassium fixation capacity and mineralogical analysis of 24 representative soils, collected from southern Iran, were studied. Potassium fixation analysis was performed by adding six rates of K from 0 to 1000 mg kg^?1 soil in a plastic beaker and shaking for 24 h. Mineralogical analysis showed that the clay fractions were dominated by smectite, chlorite, mica, palygorskite, vermiculite and quartz. In general, the studied soils fixed 8.5–55% of the added K. The potassium fixation capacity of the studied soils was significantly correlated with smectite content (r ² = 0.87), clay content (r ² = 0.60), cation-exchange capacity (r ² = 0.79) and NH₄OAc-K. Wetting and drying treatment and incubation time had significant effects on K fixation. The average percentage increase in K fixation following the wetting and drying treatment was 24 and 30% for surface and subsurface soils, respectively. The average percentage increase in K fixation with increasing residence time was 79 and 56% for surface and subsurface soils, respectively. Because K fixation is a diffusion process, time and increased concentration of soluble K (because of soil drying) are factors affecting the rate of K diffusion from a soil solution to the interlayer positions of the expansible 2:1 clay minerals.     

Chemical fractionation of phosphorus in calcareous soils of Hamedan,western Iran under different land use

We investigated the effects of land uses on P distribution and availability in selected calcareous soils under different management practices. KCl‐P (labile P), NaOH‐P (Fe‐Al‐bound P), HCl‐P (Ca‐bound P), and residual P (Res‐P) fractions at 0–30 cm depth were determined for soils planted to garlic, orchard, pasture, potato, leafy vegetables, and wheat. Trends in P distribution between chemical fractions were similar between land uses. Ca‐bound P was the most abundant P fraction in the soils, constituting between 61% and 78% of the total P, whereas P associated with labile was less abundant (< 2%). Soils under leafy vegetables and wheat along with pasture presented the highest and lowest values in all fractions of P, respectively. Labile P generally was highest for leafy vegetables and potato. Labile P and Fe‐Al‐bound P comprised < 1.4% and 8% of total P, respectively. Residual P ranged from ≈ 14% (potato and garlic) to 31% (pasture). Long‐term fertilization increased P allocation to inorganic fractions, as Ca‐bound P contained 78% of total P for potato and garlic and 74% for leafy vegetables but 61% for pasture. A strong positive correlation between labile P and Fe‐Al‐bound P (r = 0.534, p < 0.01), labile P and Ca‐bound P (r = 0.574, p < 0.01), Ca‐bound P and Fe‐Al‐bound P (r = 0.504, p < 0.01), Olsen‐P and CaCl₂‐P (r = 0.821, p < 0.01) was found. Principal‐component analysis showed that the first four components accounted for most of the variation, 32.5%, 16.9%, 12.9%, and 7.9% of total variation, respectively.     

伊朗西部不同土地利用方式下钙质土壤疏水性研究

Soil wettability and water repellency, two important soil physical properties, play an important role in water retention and water conductivity in arid and semi-arid regions. To date, there is a lack of information on soil water repellency in calcareous soils of western lran. In this study, soil water repellency and its affecting factors were studied using 20 soil series collected from Hamadan Province~ western Iran. The effects of soil properties including organic carbon content （SOC）, total nitrogen （TN）, C：N ratio, texture, CaCO3 content, and both fungal and bacterial activities on water repellency were investigated using air-dried, oven-dried and heated soil samples. Water repellency index （WRI） was determined using the short-time sorptivity （water/ethanol） method. To distinguish the actual effects of SOC, a set of soil samples were heated at 300 ~C to remove SOC and then WRI was measured on the heated samples. Relative water repellency index （RWRI） was defined as the change of WRI due to heating relative to the oven-dry WRI value. Results of the WRI values showed that the soils were sub-critically water-repellent. Pasture soils had higher WRI values compared to tilled soils, resulting from high SOC and TN, and high activities of bacteria and fungi. It was observed that SOC, TN, fungal activity, and SOC：clay ratio had significant positive impacts on WRI. Strong positive correlations of RWRI with SOC, TN and fungal activity were also observed. Pedotransfer functions derived for predicting WRI showed that the WRI values had an increasing trend with the increases in fungal activity, salinity, alkalinity and fine clay content, but showed a decreasing trend with increasing bacterial activity.     

Potassium release from sand,silt and clay fractions in calcareous soils of southern Iran

The release of non-exchangeable potassium from 24 calcareous soils of divergent mineralogy, from southern Iran, was examined. Sand, silt and clay particles were fractionated after dispersion with an ultrasonic probe. Samples were extracted with 0.01 M CaCl₂ for 30 successive 2-h periods. The clay fraction released the largest amount of K in each soil. Cumulative K released ranged from 175 to 723, 35 to 128, and 71 to 146 mg kg^?1 contributing 20–90, 4–39 and 2–54% for clay, silt and sand fractions, respectively. The lower proportion of K released from sand and silt fractions can be explained by the presence of a high content of CaCO₃ and quartz in these fractions. The release kinetics for the non-exchangeable K data showed that parabolic diffusion and power function were the best fitting kinetic models. This indicated that slow diffusion of K from the mica interlayer positions is the main rate-controlling process. Cumulative K released and constant b values of parabolic diffusion model correlated significantly with the mica content of the clay fraction.     

pH对土壤重金属吸附动力学的影响

The pH effect on the sorption kinetics of heavy metals in soils was studied using a constant flow leaching method. The soil samples were red soil collected from Yingtan, Jiangxi, and yellow-brown soil from Nanjing, Jiangsu. The heavy metals tested were zinc and cadmium. Assuming that the experimental data fitted to the following kinetic rate equation: 1/c·dx/dt = kx_∞-kx, the rate constant k of sorption could be determined from the slope of the straight line by plotting of 1/c·dx/dt vs. x. The results showed that the pH effect on the rate constants of heavy mental sorption in soils was very significant. The values of k decreased with increasing pH. The sorptions were more sensitive to pH in red soil than in yellow-brown soil.     

Adsorption isotherms of some heavy metals under conditions of their competitive adsorption onto highly calcareous soils of southern Iran

Recently, application of sewage sludge or effluents resulted in raising the concentrations of some heavy metals in some agricultural soils of Iran. Experiments were conducted to evaluate the competitive adsorption of lead (Pb), copper (Cu), zinc (Zn), and cadmium (Cd) on six calcareous soils. Adsorption characteristics were evaluated by equilibration of 1 g of each soil sample with 20 ml of 0, 10, 20, 30, 40, 50, 100, or 200 mg L^?1 of their nitrate solutions and 0.01 M NaNO₃ as background electrolyte. Furthermore, solid/liquid distribution coefficients (K_d) of studied metals, as an index of soil capacity to resist a change of the soil solution concentration, were calculated. Results indicated that amounts of adsorbed Pb, Cu, Zn, and Cd increased with increase in their concentrations in the contact solutions, but this trend was more pronounced for Pb and Cu than the others. For all studied soils and metals, Langmuir equation described the adsorption behavior fairly well. Furthermore, Langmuir and Freundlich equation parameters were positively correlated to cation exchange capacity (CEC) and smectite contents; whereas, they were negatively correlated to sand content. Considering K_d values, the selectivity sequence of the metal adsorption was Pb > Cu > Zn > Cd. Therefore, the risk of leaching and also plant uptake of Zn and Cd will be higher as compared to those of the other elements.     

Transformation kinetics of inorganic P forms in relation to calcareous soil properties of western Iran

This study was conducted to investigate the effect of time on chemical forms of P in 10 calcareous soils of western Iran. Phosphorus was added to soils at the rate of 200 mg kg^?1 as KH₂PO₄. The samples were incubated for 1, 7, 15, 30, 60, 90 and 120 days at 25°C and constant moisture. After incubation, P was fractionated by the sequential extraction procedure: soluble and exchangeable P (NaHCO₃-P) Al + Fe-P (NaOH-P), Ca-P (HCl-P) and residual P (Res-P). The distribution of added P into different fractions consisted of two phases involving initial rapid retention followed by a slow continuous retention. In general, the majority of the P applied entered mostly in the HCl-P and Res-P fractions. After 120 days incubation, the HCl-P fraction remained the most dominant in all soils. A combination of silt and sand content of the soils together explained between 88.5 and 83.3% of the variance inNaHCO₃-P and HCl-P transformation rates, respectively, 76.6 and 72.8% of which is explained by silt alone. CaCl₂-P and electrical conductivity (EC) together accounted for 66.3% of the variation in the rate constant of NaOH-P. The release rate of Res-P was not significantly related to soil properties.     

长期施磷对土壤磷素吸附演变的影响

Knowledge of phosphorus （P） behavior in long-term fertilized soils is essential for programming fertilization practices and for sustaining environmental quality. The long-term （1984-1997） effects of various fertilization treatments on P changes and sorption isotherms as well as the relationship of soil properties to P sorption and P forms were evaluated in an Ustic Isohumisol, a calcareous soil, on the Loess Plateau, China. Compared to 1984, after 13 years of crop production, total soil P in the no-P treatments （control and N treatment） decreased by 5%-7%, but in the phosphorus fertilizer alone （P）, nitrogen and phosphorus fertilizers in combination （NP）, manure alone （M）, and nitrogen and phosphorus fertilizers and manure in combination （NPM） treatments, it increased by 22%, 19%, 28%, and 58%, respectively. Residual fertilizer P was found mainly in NH4Ac-soluble P （Cas-P）, followed by NaHCO3-soluble P （NaHCO3-P）, and NH4F-soluble P （Al-P）. Phosphorus sorption in the soils with different fertilization practices fit the Langmuir equations. Phosphorus sorption capacity in the no-P treatments increased, whereas it decreased in the P-included treatments （P, NP, and NPM treatments）. Phosphorus sorption maximum （Qm） was significantly and negatively correlated to inorganic P including NaHCO3-P, Cas-P, NaOH-Na2CO3-soluble P （Fe-P）, and Al-P （P ≤ 0.01）. Moreover, long-term fertilization increased soil organic carbon in the NP, M, and NPM treatments and decreased pH in the NP and NPM treatments. Thus, the ability of the soil to release sorbed P to the environment increased under long-term P fertilization.     

Kinetics of nonexchangeable‐potassium release and plant response in some calcareous soils

Nonexchangeable K⁺ constitutes a slowly available reserve that may significantly influence K⁺ fertility of soils. Laboratory and greenhouse experiments were conducted to characterize the K⁺ supply and nonexchangeable K⁺–release kinetics in 10 calcareous soils using 0.01 M CaCl₂ and 0.01 M oxalic acid extractions. Total K⁺ uptake by wheat (Triticum aestivum L.) grown in the greenhouse was used to measure plant‐available K⁺. The release of K⁺ was characterized by an initial fast rate followed by a slower rate. The nonlinear relationship in the early stages of the K⁺ release may be attributed to the edge sites, and release of K⁺ from interlayer exchange sites may be responsible for the second part of the K⁺ release. Kinetics of K⁺ release was described best with power function, which showed the best fit of the four models tested. Parameters of kinetics models in 0.01 M CaCl₂ were significantly related to K⁺ uptake by wheat. Potassium release was also correlated to initial NH₄OAc‐extratable K⁺ and to HNO₃‐extractable K⁺.     

Kinetics of phosphorus release from calcareous soils under different land use in Iran

The rate of phosporus (P) release from soils can significantly influence P fertility of soils. The objectives of this study were to investigate the effects of land‐use types on the kinetics of P release under different management practices and the relationship between kinetic parameters and soil physical and chemical properties from calcareous soils. The kinetics of P release in 0.01 M CaCl₂ was studied in surface samples of 30 calcareous soils planted to garlic, garden, pasture, potato, vegetables, and wheat. Trend in P‐release kinetics was similar between land‐use types. Significantly different quantities of P were released under different land use. The maximum amount (average of five soils) (46.4 mg kg^–1) of P was released in soil under potato and the minimum amount (10.4 mg kg^–1) under pasture. The kinetics of P release from soils can be described as an initial rapid rate followed by a slower rate. Different models were used to describe P release. In general, parabolic diffusion and power equation were found to be appropriate for modeling P release. The P‐release rate for the soils was estimated by parabolic equation for the studied land‐use types. The constant b was lower for pasture and wheat than for garlic and potato. The relationship between the rate of P release with Olsen‐P was linear, while it was curved with respect to the CaCl₂‐P, indicating that release of P was diffusion‐controlled. When the kinetic parameters of models were regressed on soil properties, CaCl₂‐P and CaCO₃ appeared to be the most important soil properties influencing P‐release rates in these soils.     

Effects of equilibrating salt solutions on phosphate sorption by soils

Abstract

Several equilibrating salt solutions have been used in the studies of P sorption by soils and sediments. This study was conducted to evaluate the effects of 10 salt solutions on estimation of P sorption by soils. Results obtained showed that, when the equilibrating solution was made to contain 0.01M with respect to CaCl₂, Ca(NO₃)₂, CaSO₄, MgCl₂, KCl, LiCl, Nacl, or KHCO₃, the amount of P sorbed by soil always exceeded the amount sorbed from the soil‐water system. In comparison with the amount of P sorbed from water, 0.01M NaHCO₃ reduced P sorption by soils. Use of THAM buffer (0.05M pH 7.0) to control the pH increased P sorption by some soils and decreased P sorption by others, relative to that sorbed from the soil‐water system. The results indicated that inclusion of salts in the equilibrating solution for P‐sorption studies should be avoided, especially in studies related to water quality.     

An evaluation of methods for characterizing phosphate sorption in rice soils

Abstract

Two single value methods of indexing P sorption were compared to parameters derived from P adsorption isotherms in a range of waterlogged and dry rice soils. These measures of P sorption capacity correlated closely with one another. However, they did not correlate equally with several other soil properties (pH, extractable Fe and Al). Because relationships between P sorption and soil properties proved to be method dependent, results from different methods must be compared with caution.

It is suggested that the single value method of Bache and Williams² be adopted when the rapid analyses of many samples is required. It is suited to routine analysis of soils with markedly different P sorption capacities, from both waterlogged and dry conditions.

Close correlations between the single value methods and P sorbed at a standard supernatant concentration suggest they may be useful in testing soils for P fertilizer requirements.     

电解质浓度对土壤吸附铜离子时氢离子释放的影响

研究了不同铜离子浓度、不同电解质浓度情况下,吸附铜离子时氢离子释放对两种可变电荷土壤和4种恒电荷土壤悬液pH的影响。研究结果表明,除了黄棕壤外,含铁量越高,由于吸附铜离子后所引起的土壤ΔpH最大值越小。加入的铜离子浓度为10-4molL-1时,铜离子吸附对中和曲线形状没有根本影响。在较低浓度时,铜离子吸附时氢离子的释放较少;而在较高浓度时,当体系pH值大于一临界值时,开始释放大量氢离子。氧化铁是引起恒电荷土壤和可变电荷土壤在吸附铜离子时氢离子释放差异产生的主要原因。电解质浓度的变化对恒电荷土壤和可变电荷土壤吸附铜离子后中和曲线变化影响有很大的区别,含铁量越高,电解质浓度对土壤吸附铜离子后的氢离子释放的影响越小。     

Influence of soil applied boron on yield of berseem (Trifolium alexandrium L.) and soil boron fractions in calcareous soils

A greenhouse experiment was conducted in North-west India to study the effect of soil applied boron on yield of berseem (Trifolium alexandrium L.) and soil boron fractions in boron deficient calcareous soils. Three soils with varying calcium carbonate content viz. 0.75% (Soil I), 2.6% (Soil II), and 5.7% (Soil III) were collected from different sites of Ludhiana, Bathinda, and Shri Muktsar Sahib districts, Punjab, India. The treatments consisted of six levels of soil applied boron viz. 0.5, 0.75, 1.0, 1.25, 1.5, and 2.0 mg B kg^?1 along with control. The green fodder yield and dry matter yield increased significantly at 0.75 mg B kg^?1 soil treatment level in the first cutting, while these were significant at 1.0 mg B kg^?1 soil treatment level in all soils at second, third, and fourth cuttings. Among all three calcareous soils, Soil I with lower calcium carbonate was the best soil in respect of mean yield in comparison to Soil II and Soil III. Combined effect of boron level and soils had significant effect on yield of berseem. There was a significant increase in mean dry root biomass at 1.0 mg B kg^?1 soil level over control and then remained non-significant with further high levels of soil applied boron. The mean dry root biomass decreased significantly for the soils having 0.75%, 2.6%, and 5.7% calcium carbonate levels. Readily soluble fraction is considered to be easily available fraction of B for plant uptake and consisted of 0.47–0.62% in Soil I, 0.31–0.43% in Soil II, and 0.24–0.34% in Soil III of the total boron. Among all B fractions, mean readily soluble, specifically adsorbed, and oxide-bound fractions got increased significantly with increase in B levels. Readily soluble and organically bound B fractions were more in Soil I as compared to Soil II and Soil III. Specifically adsorbed boron, oxide bound fraction, residual and total boron were more in Soil III in comparison to Soil I and Soil II. Among all fractions, residual fraction accounted for the major portion of the total B. It comprised of 92.71–93.90% in Soil I, 94.51–95.40% in Soil II, and 94.91–95.25% in Soil III of the total boron.     

Barley responses to copper foliar spray concentrations when grown in a calcareous soil

This study was designed to determine the adequate copper (Cu) foliar spray concentration to correct Cu deficiency on barley (Hordeum vulgare L.) when grown in a calcareous soil. Five Cu foliar spray solution levels were tested (0% or control; 0.03%, 0.06%, 0.13%, and 0.33%). Copper was applied in the sulfate form at the early boot stage. The results showed that Cu flag leaf concentration was increased with the highest Cu application (0.33%), while Cu concentration in the grain was increased with a spray of 0.03%. An antagonism between Cu, Zn, and Fe leaf concentration was observed. Grain yield and harvest index showed a linear positive response to Cu foliar spray concentrations. A significant increase of 19.6% on grain yield was recorded with a foliar spray 0.33% of Cu.     

Effect of reducing conditions on P sorption of soils

Abstract

The phosphate sorption (P _sor) capacity of soils increased when the soils were reduced (Willet and Higgins, Aust. J. Soil Res., 16, 319–326, 1978). The present study aimed at the elucidation of this mechanism using Na₂S₂O₄ and 5 different soils. The P _sor of the 5 soils increased with the addition of a small amount of Na₂S₂O₄. Fe(II) was released from the soils with the addition of the same small amount of Na₂S₂O₄. Furthermore, when the amount of FeCl₂ corresponding to the amount of Fe(II) released along with the small amount of Na₂S₂O₄ was added, the P _sor of the soil increased. However, the P _sor of the lowland soils, of which the hydrous Fe oxide content was lower than the others, decreased when the amount of Na₂S₂O₄ addition was increased up to 150–200 g kg^?1. Based on these results, the following process is inferred for the increase in the P _sor of the soils when they are reduced. Hydrous Fe oxide in soil takes the form of very fine, high-density particles and reacts with P mainly on their surface. When a small amount of Na₂S₂O₄ is added, the hydrous Fe oxide is partially reduced, dissolved and finally re-precipitates with P by oxidation with O₂ from the air during the experiment.     

Ability of sorption–desorption experiments to predict potassium leaching from calcareous soils

When potassium (K⁺) fertilizers are applied to the soil, K⁺ is subject to displacement through the soil profile. Leaching can play an important role in agricultural K⁺ losses that can decrease groundwater quality. To avoid overfertilization, estimation of K⁺ leaching from soil is important. The ability of the soils to retain K⁺ against leaching varies according to the adsorption coefficient of the soils. The aim of this study was to relate the K⁺ leaching from a wide range of calcareous soils to the values obtained from a sorption–desorption experiment. The soil columns were leached with 10 mM CaCl₂ solution and the leachate was analyzed for K⁺. The breakthrough curves for K⁺ were different, and the amounts of K⁺ leached varied considerably between different soils. In these calcareous soils where crops are irrigated with water containing significant concentrations of Ca²⁺ and other cations, large amounts of K⁺ will be leached. Cumulative K⁺ leached after five pore volumes leaching with 10 mM CaCl₂ was significantly (r = 0.776, p < 0.01) related to the equilibrium K⁺ concentration. The results of this study enabled us in many cases to estimate the K⁺ leaching from soil without conducting column experiments, minimizing the laborotary work.