动力学模型在土壤钾素释放特征描述中的运用及其与化学方法提取的钾素之间的相关性研究

Potassium (K) release characteristics in soil play a significant role in supplying available K. Information on K-release characteristics in soils of central Iran is limited. The objectives of this study were to determine K release characteristics and correlations of K release rate constants with K extracted by different chemical methods in surface soils of ten calcareous soils of central Iran. The kinetics of K release in the soils was determined by successive extraction with 0.01 mol L^-1 CaCl₂ in a period of 2--2 017 h at 25±1 ^oC. Soil K was extracted by distilled water, 0.5 mol L-1 MgNO₃, 0.002 mol L^-1 SrCl₂, 0.1 mol L^-1 BaCl₂, 0.01 mol L^-1 CaCl₂, 1 mol L^-1 NaCl, 1 mol L^-1 boiling HNO₃, 1 mol L^-1 NH₄OAC, Mehlich 1, 0.002 mol L^-1 SrCl₂ 0.05 mol L^-1 citric acid, and ammonium bicarbonate-diethylenetriamine pentaacetic acid (AB-DTPA). A plot of cumulative amounts of K released showed a discontinuity in slope at 168 h. Thus, two equations were applied to two segments of the total reaction time (2--168 and 168--2017 h). Cumulative amounts of K released ranged from 55 to 299 mg kg^-1 in 2--168 h and from 44 to 119 mg kg^-1 in 168--2 017 h. Release kinetics of K in the two time segments conformed fairly well to parabolic diffusion, simplified Elovich, and power function models. There was a wide variation in the K release rate constants. Increasingly higher average concentrations of soil K were extracted by distilled water, Mehlich 1, SrCl₂, CaCl₂, SrCl₂ + citric acid, AB-DTPA, MgNO₃, NaCl, NH₄OAc, BaCl₂ and HNO₃. Potassium release rate constants were significantly correlated with K extracted. The results of this study showed that information obtained from mathematical modeling in two reaction time segments can help to estimate the K-supplying power of soils.     

Soil Potassium‐Release Characteristics and the Correlation of its Parameters with Garlic Plant Indices

Abstract

Potassium (K)‐release characteristics (PRC) of soil play a significant role in supplying available K. Information about PRC in the Hamadan soils is limited. The objective of this research was to study the PRC in nine soils from the Hamadan province by successive extraction with 0.01 M CaCl₂ over a period of 2000 h. The correlation of kinetic equation rate constants with soil properties and garlic indices was also studied. The release of K was initially rapid. More than 60% of the total K released during the first 168 h. The amount of K released after 168 h varied among soils and ranged from 292.8 to 736.8 mg kg^?1. The amount of K released after 2000 h was significantly correlated with K extracted by 1 M HNO₃, 0.01 M CaCl₂, and 0.1 M BaCl₂, whereas it was not significantly correlated with other soil properties. Potassium‐release characteristics were evaluated using five kinetic equations. Statistical analysis showed that the Elovich equation described the K‐release kinetics. A plot of other equations shows a discontinuity in slope at 168 h. Thus, two equations were applied to segments of the total reaction time (2 to 168 and 168 to 2000 h). The release‐rate constants (slope) in segment 1 are higher than in segment 2. The release‐rate constant of the Elovich equation and the zero‐order equation in two segments were significantly correlated with 1 M HNO₃, 0.01 M CaCl₂, and 0.1 M BaCl₂. Rate constants of the other equations were not significantly correlated with soil properties. The release‐rate constants of the Elovich equation and release‐rate constants of the zero‐order equation in two segments were significantly correlated with garlic indices. Rate constants of other equations were not significantly correlated with garlic indices. The results of this research showed that the Elovich and zero‐order equations can be used to describe K‐release characteristics.     

Impact of Poultry Manure Application on Phosphorus Desorption in Some Calcareous Soils

Laboratory experiments were conducted to study the kinetics of phosphorus (P) desorption in different calcareous soils of Hamadan Province of Iran. Soils were fertilized with poultry manure at 50 ton ha^–1 and incubated at 25 ± 1 °C at 15% moisture for 6 months. The release rate of P was studied by successive extraction with 0.5 M sodium bicarbonate (NaHCO₃) over a period of 1–1752 h. Also, available P was determined. The results showed that available P in fertilized and unfertilized soils ranged from 13.3 to 55.1 and 10.0 to 50.1 mg kg^–1, respectively. Phosphorus desorption from the fertilized and unfertilized soils began with a fast initial reaction, followed by a slow secondary reaction. The amount of P released after 1752 h in fertilized and unfertilized soils ranged from 319.2 to 623.9 and 309 to 586.7 mg kg^–1, respectively. The amount of P released was significantly correlated with available P. The kinetics of cumulative P release were evaluated using the five kinetic equations. Phosphorus desorption kinetics were best described by the parabolic diffusion law, first order, and power function equations. Rate constants of these equations different in fertilized and unfertilized soils.     

Release Kinetics of Nonexchangeable Potassium by Different Extractants from Soils of Varying Mineralogy and Depth

Abstract

Nonexchangeable potassium (K) release kinetics of six major benchmark soil series of India as affected by mineralogy of clay and silt fractions, soil depth and extraction media was investigated. The cumulative release of nonexchangeable K was greater in smectitic soils (353 mg K kg^?1 at 0‐ to 15‐cm depth and 296 mg K kg^?1 at 15‐ to 30‐cm depth, averaged for 2 soils and 3 extractants) than in illitic (151 mg K kg^?1 at 0‐ to 15‐cm depth and 112 mg K kg^?1 at 15‐ to 30‐cm depth) and kaolinitic (194 mg K kg^?1 at 0‐ to 15‐cm depth and 167 mg K kg^?1 at 15‐ to 30‐cm depth) soils. Surface soils exhibited larger cumulative K release in smectitic and illitic soils, whereas subsurface soils had larger K release in kaolinitic soils. Among the extractants, 0.01 M citric acid extracted a larger amount of nonexchangeable K followed by 0.01 M CaCl₂ and 0.01 M HCl. The efficiency of citric acid extractant was greater in illitic soils than in smectitic and kaolinitic soils. Release kinetics of nonexchangeable K conformed fairly well to parabolic and first‐order kinetic models. The curve pattern of parabolic diffusion model suggested diffusion controlled kinetics in all the soils, with a characteristic initial fast rate up to 7 h followed by a slower rate. Greater nonexchangeable K release rates in smectitic soils, calculated from the first‐order equation (b=91.13×10^?4 h^?1), suggested that the layer edge and wedge zones and swelling nature of clay facilitated the easier exchange. In contrast to smectitic soils, higher release rate constants obtained from parabolic diffusion equation (b=39.23×10^?3 h^?1) in illitic soils revealed that the low amount of exchangeable K on clay surface and larger amount of interlayer K allowed greater diffusion gradients, thus justifying the better fit of first‐order kinetic equation in smectitic soils and parabolic diffusion equation in illitic soils.     

Potassium Fixation and Release Characteristics of Several Normal and K-Exhausted Soils in the Middle and Lower Reaches of the Yangtse River,China

Potassium (K) fixation and release in soil are important factors affecting K availability to plants and the utilization efficiency of K fertilizer. Three typical soils (red soil, yellow cinnamon soil, and alluvial soil) were collected from the middle and lower reaches of Yangtse River, China, to study the K-fixation and K-release characteristics of the normal and K-exhausted soil. Results showed that K fixation of added K in K-exhausted soils were significantly (P < 0.05) greater than that of the normal soils. There were significantly (P < 0.05) negative correlations among K-fixation capacity, concentration of soil-available K, and K⁺ saturation. Irrespective of soil K exhaustion, K fixation of added K was in the order of red soil > yellow cinnamon soil > alluvial soil, but the cumulative amount of K released from the three soils during successive extractions with 1.0 mol L^?1 nitric acid (HNO₃) was in the opposite order. The cumulative amounts of K released with 1.0 mol L^?1 ammonium acetate (NH₄OAc) and 1.0 mol L^?1 HNO₃ extraction increased with the increasing numbers of extractions. The K-releasing power of soil by successive extraction decreased gradually and finally became almost constant. The release of K was lower in K-exhausted soil than in normal soil. Overall, the information obtained in this study will be helpful in formulating more precise K fertilizer recommendations for certain soils.     

Effect of Bean (Phaseolus vulgaris L.) Rhizosphere on Zinc-Release Kinetics

The primary factor that influences release of zinc (Zn) for plants is the rhizosphere. However, information about Zn-desorption characteristics in the rhizosphere is limited. A greenhouse experiment was performed to determine Zn-release characteristics in the bulk and the rhizosphere soils using a rhizobox. The kinetics of Zn release was determined by successive extraction with diethylenetriaminepentaacetic acid (DTPA)– triethanolamine (TEA) in a period of 1 to 504 h at 25 ± 1 °C in the bulk and the rhizosphere soils. Moreover, Zn extracted by using three extractants [DTPA-TEA, ammonium bicarbonate (AB)-DTPA, and Mehlich 3] in the bulk and the rhizosphere soils. The results showed that Zn extracted in the rhizosphere soils were significantly (P < 0.01) lower than the bulk soils. The mean of Zn release in the bulk and the rhizosphere soils were 5.31 and 4.91 mg kg^?1, respectively. Release kinetics of Zn conformed fairly well to power function, first order, parabolic diffusion, and simplified Elovich equations. The results of kinetics study indicated that release-rate coefficients decreased in the rhizosphere soils compare to the bulk soils. The correlation studies showed that Zn release after 504 h was significantly correlated (P < 0.05) with Zn extracted by using DTPA-TEA, AB-DTPA, and Mehlich 3 in the bulk and the rhizosphere soils. The results of this research showed that Zn-release characteristics in the bean rhizosphere soils were different from the bulk soils.     

土壤非交换性钾释放动力学特征及其生物

采用生物耗竭法和0.2mol L-1的NaTPB化学浸提法,利用不同动力学方程对我国8种主要土壤非交换性钾的释钾特性及其生物有效性进行定量评估。结果表明,供试土壤非交换性钾释放分为快速释放和稳定释放两个阶段,一级动力学方程、Elovich 方程、双常数曲线方程和抛物线扩散方程均能描述土壤非交换性钾的释放过程。根据双常数方程中的参数（a）所表征的土壤非交换性钾释放速率常数,供试8种土壤的释钾能力按取土地区存在着自西向东、自北向南渐减的趋势。盆栽试验中,在累积释钾量高且释放速率快的土壤上,黑麦草累积生物量、累积吸钾量和相对含钾量较高,表现出强的供钾能力;与此相反,累积释放量低且释放速率慢的土壤上,黑麦草各项指标偏低,供钾能力较弱。以黑麦草钾素丰缺临界值34.00 mg kg-1 DW-1和土壤非交换性钾释放速率396.32 mg kg-1 h-1作为评价指标,供试8种土壤中,仅取自新疆石河子、陕西常武和黑龙江哈尔滨地区的土壤在短期不施用钾肥的情况下能保证黑麦草丰产且不出现缺钾症状。因此,为了维持土壤钾素平衡和保证作物高产稳产,在我国西北、东北地区耕地土壤中应加强秸秆的循环利用,而在华中和华东地区则需增施钾肥和有机肥。     

Release of potassium from some benchmark soils of India

Release of potassium from 15 surface samples of benchmark Alluvial, Red and Black soils of India to 0.01 M solutions of BaCl₂, CaCl₂, NH₄Cl and NaCl was studied in soils either untreated or pretreated with 5 × 10⁻³ M KCl. In the untreated soils, the efficacy of the extractants declined in the sequence: BaCl₂ > NH₄Cl > CaCl₂ > NaCl. Cumulative K-release was greatest from Black soils, followed by Red and Alluvial soils. From soils pretreated with 5 * 10⁻³ M KCl, more K was released than retained, and more 'native' K was released than that from untreated soils. Increase in the release of 'native' K decreased in the sequence: Red > Alluvial > Black soils. The amounts of surface and internal K, desorption rate constants and parabolic diffusion constants were calculated from K release to the various electrolytes.     

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.     

The release of nonexchangeable potassium from certain soils of northern Greece

The release of nonexchangeable potassium from the surface layers of nine red soils, sampled in different districts of northern Greece, was studied by treatment of the samples with H⁺-resin at various soil: resin ratios and temperatures and in a pot-experiment with rye grass. It was thus found that, the phenomenon of K-release from the soil samples during their treatment with the H⁺-resin, follows typically the kinetics of the first order opposing reactions under all conditions tested. A close relationship was shown to exist between nonexchangeable potassium released by cropping (defined as K-supplying capacity of the soil) and that released by treatment with the resin. The K-supplying capacity of the soils studied seems to be more closely related to the total amount of lattice-K released by the resin than to the rate of the release. The latter is affected considerably not only by temperature changes but also by changes in the soil:resin ratio. A value for the activation energy of the release reaction was calculated which might be considered as lending additional support to the view, already widely accepted, that K-release in the soil is a diffusion-dependent phenomenon.     

Kinetics of Soil Potassium Release Under Long-Term Imbalanced Fertilization in Calcareous Soils

Knowledge on potassium ion(K~+) release from soils makes K fertilizer recommendation more efficient and profitable.Kinetics of K~+release under continuous fertilization of no fertilizer(CK), urea(N), triple superphosphate(P), and urea + triple superphosphate(NP) without K fertilizer was investigated in calcareous(chloritic and kaolinitic) soils on the Miandarband Plain in Kermanshah Province of Iran.The results showed that the kinetics of K~+release included an initial reaction and a slow reaction.The phosphateand NH_4~+-induced K~+release followed the same rate process during the rapid(2–192 h) and slow release periods(192–1 090 h).There were no significant differences in the cumulative K~+released from the chloritic and kaolinitic soils among all the treatments.The cumulative K~+released was positively correlated with P adsorption capacity for the chloritic(r = 0.461, P 0.05) and kaolinitic soils(r = 0.625, P 0.01), and negatively correlated with K fixation potential for the chloritic(r = 0.720, P 0.01) and kaolinitic soils(r =-0.513, P 0.01).There was a significant(P 0.001) interactive effect of K fixation potential × P adsorption capacity on the cumulative K~+released for both soil groups.The initial release rate(IRR) index(a·b, where a and b are the rate coefficients of the power function equation) for the chloritic soils was significantly(P 0.05) higher under applications of P and NP than N and CK.The IRR index values among different fertilization treatments were in the order of NP = P N = CK for the chloritic soils, and N =P NP CK for the kaolinitic soils.This study showed that K fixation potential and P adsorption capacities controlled K~+release from soils.This information will be helpful for precise fertilizer recommendations for the studied soils.     

Zinc Release Characteristics from Calcareous Soils using Diethylenetriaminepentaacetic Acid and Other Organic Acids

Adsorption and desorption reactions of zinc (Zn) in soils control its availability to plants. In the present investigation, time-dependent Zn release was evaluated using three organic acids [diethylenetriaminepentaacetic acid (DTPA), citric acid, and maleic acid] to depict the Zn fraction controlling Zn release rate from slightly calcareous to calcareous soils. Eight surface and two subsoil samples of selected soil series varied in their physicochemical properties, amount of Zn held in different chemical pools, and Zn-retention capacities (21–61%). Each soil was extracted for a total period of 24 h at 1:10 soil/extractant suspension ratio using 0.005 M DTPA. The time-dependent parabolic diffusion model best described the Zn release in six consecutive extractions. Soils differed in cumulative Zn extracted (1.09–3.81 mg kg^?1 soil) and Zn release rate. Under similar conditions, three soils differing in Zn-retention capacities were also extracted with five different concentrations (0.01–0.0001 M) of citric and maleic acids. Although both maleic and citric acids released soil Zn at greater rates and in greater amounts than DTPA, maleic acid was more efficient. Soil Zn bound to amorphous iron (Fe) + manganese (Mn) oxides was the main Zn pool that controlled Zn release characteristics.     

Potassium Release Kinetics in Potato Growing Alluvial Soils of North Western India

Potassium (K) release and kinetics were studied in soils of north western India varying in soil properties. Mathematical equations were tested for their applicability to describe K release in the alluvial soils. The major portion of total K was released within 1 h of the reaction. The initial rapid K release was followed by a slower rate of K release. The linear equation adequately described the K release kinetics. The next best fit to satisfactorily describe the reaction rates of K release was the first order equation. There existed two separate first order equations indicating different rates of K release. Soils having higher native potassium and clay released higher amounts of K and at a faster rate. However, the first order equation showed that the faster rate of reaction might be inhibited by higher amounts of clay, probably because of the restrictive properties of illites.     

Continuous Cropping,Fertilization, and Organic Manure Application Effects on Potassium in an Alfisol under Arid Conditions

Effects of continuous cropping and addition of organic manures (farmyard manure, FYM, and groundnut shells, GNS) along with inorganic fertilizers on nonexchangeable potassium (K) release kinetics in a K-deficient Alfisol were studied in a 20-year manurial experiment under arid conditions. There was a depletion in available K under continuous cropping without K input (control) as compared to other treatments such as 100% nitrogen–phosphorus–potassium (NPK), 50% NPK + 4 metric tons (MT) groundnut shells ha^?1, 50% NPK + 4 MT FYM ha^?1, and 100% organic (i.e., 5 MT FYM ha^?1). Over 20 years of cropping without K input, available K was reduced from 155 kg ha^?1 (in 1985) to 82 kg ha^?1 (in 2005), showing a negative balance of 73 kg ha^?1. Soil in control plots showed available K in the deficient range (<50 mg kg^?1), whereas four other fertilizer and manurial treatments were greater than the critical limit. Considerable improvements in nonexchangeable K-release parameters such as step K and cumulative K release were observed in manured plots over control. Parabolic diffusion and first-order kinetic equations explained K release from soils. Potassium-release rates were drastically reduced in control plots, and there were increased release rates with continuous addition of manures. Results suggest that soils with groundnut shells or FYM (4 MT ha^?1) along with 50% inorganic fertilizer additions could maintain greater K release rates after 20 years of cropping as compared to cropping without K input.     

钾解吸动力学方程及方程常数的应用

Elovich,parabolic diffusion,power function and exponential equations were used to describe K desorption kinetics of 12 soils in a constant electric field of electro-ultrafiltration(EUF),Results showed that the Elovich,parabolic diffusion and power function equations could describe K desorption kinetics well owing to their high correlation coefficients and low standard errors;but the exponential equation was not suitable to be used in this study due to its relatively low correlation coefficients and relatively high standard errors.This work established successfully the relationships between the constants(slope or intercept)of kinetic equations and the barley responses to K fertilizer in the multiple-site field experiments and K-supplying status of soilsk,the constants of Elovich,parabolic diffusion and power function equations were very significantly or significantly correlated to the soil available K,relative yield of barley and K uptake of barley in NP plot.It was suggested that the kinetic equation constants could be used to estimate K-supplying power of soils.     

Release of Soil Nonexchangeable K by Organic Acids

The amounts of soil nonexchangeable K extracted with 0.01mL/L oxalic acid and citric acid solutions and that with boiling 1mL/L HNO3 for ten minutes were remarkably significantly correlated with each other,and the amount extracted with the oxalic acid solution was higher than that with the citric acid solution.The soil nonexchangeable K release was comprised of two first-order kinetic processes.The faster one was ascribed to the interlayer K in outer sphere,while the slower one to that in inner sphere.The rate constants of the soil nonexchageable K were significantly correlated with the amounts of nonexchangeable K ex tracted with boiling 1mL/L HNO3 for ten minutes.Study on the fitness of different kinetic equations indicated that the first-order,parabolic diffusion and zero-order equations could all describe the release of soil nonexchangeable K well,but Elovich equation was not suitable to describe it.     

Evaluation of copper desorption characteristics using DTPA and citric acid for wheat (Triticum aestivum L.) rhizosphere of soils amended with sewage sludge

A greenhouse experiment was carried out to determine copper (Cu) desorption characteristics in ten bulk and rhizosphere soils (Typic Calcixerepts) amended with sewage sludge (1% w/w) using rhizoboxes. The kinetics of Cu desorption in the bulk and the rhizosphere soils were determined after successive extraction with DTPA‐TEA and 10 mM citric acid in a period of 1 to 504 h at (25 ± 1)°C. The results show that Cu extracted after 504 h using DTPA‐TEA were significantly (P < 1%) lower in the rhizosphere than the bulk soils. However, Cu extracted after 504 h using citric was significantly (P < 1%) higher in the rhizosphere than in the bulk soils. The results illustrated that, on average, citric acid extracted 56% more Cu from the bulk soils than DTPA‐TEA, and citric acid extracted 85% more Cu from the rhizosphere soils than DTPA‐TEA. Desorption kinetics of Cu in the two extractants was well described by power‐function, parabolic diffusion, and first‐order equations. The results show that a 10 mM citric acid extractant may be recommended to determine the kinetics of Cu desorption in calcareous soils amended with sewage sludge.     

Potassium Quantity–Intensity Parameters and Their Correlation with Bean Plant Indices in Some Calcareous Soils

Plant availability of potassium (K) in soils is controlled by dynamic interactions among its different pools. Potassium quantity–intensity (Q/I) parameters were determined to relate them to bean plant indices in a pot experiment. The results showed that the activity ratio at equilibrium (AR^k) ranged from 0.015 to 0.358 (mmol L^?1)^0.50, the potential buffering capacity (PBC) ranged from 7.54 to 26.32 mmol kg^?1/(mmol L^?1)^0.50, the labile K (Δk°) ranged from 9.1 to 112.2 mg kg^?1, and the K adsorbed at specific sites (Kx) ranged from 6.51 to 69.69 mg kg^?1. The results of pot experiment showed that some K Q/I parameters were significantly correlated with some plant indices. Also, the correlation study showed that readily exchangeable K was significantly correlated with K Q/I parameters except K_x. The results of this research show that the K Q/I method can be used for estimating of soil K availability for bean.     

土壤钾解吸的动力学方程和大麦反应的关系

本文应用Ｅｌｏｖｉｃｈ、抛物线扩散、权函数和指数方程研究电超滤恒电场下１２种土壤钾解吸的动力学。Ｅｌｏｖｉｃｈ、抛物线扩散和权函数方程具有高的相关系数和小的标准差，可以很好地描述土壤钾解吸的动力学，而指数方程的相关系数低和标准差大而不适宜应用。本文成功地建立了动力学方程与大麦多点田间试验钾肥反应和土壤钾素状况之间的相关关系，Ｅｌｏｖｉｃｈ、抛物线扩散和权函数方程的常数（斜率或截距）与土壤速效钾、大     

Mathematical models to study the kinetics of potassium release from swell-shrink soils of Central India in relation to their mineralogy

Employing four mathematical models (first-order, parabolic-diffusion, Elovich and zero-order), kinetics of potassium desorption from eight soils with and without cropping were studied to evaluate their ability in explaining K release from soils. The decline in the soil test K in cropped soils over original soils was drastic in easily desorbable forms compared to that of strongly held forms like 3 M H₂SO₄ K. Results showed that parabolic diffusion as well as first-order kinetic equation explained the K release data well for both original and K depleted (cropped) soils. Elovich and zero-order equations were not suitable to describe the kinetic data. However, zero-order equation explained K release data better in case of K-depleted soils as compared to original soils. Soils with higher initial K contents registered higher release rate constants. Over the entire period of cropping the range of release rate (b) decreased from 1.26 to 1.53 × 10^?2 to values ranging from 1.12 to 1.30 × 10^?2 h^?1. In contrast, the first-order equation, parabolic diffusion showed higher b values for cropped soils as they represent the diffusion gradient. Mica and its biotite content in both silt and clay fractions showed significant correlation (r) with b values. Similarly with the rate of K release, clay content of soils maintained significant r whereas the silt content did not.