Extraction of soil phosphorus with calcium chloride solution for prediction of plant availability

Abstract

Soil and vegetative samples of ley and cereals were collected four times during the growing season from field and pot trials with different phosphorus (P) fertilisation levels. The soil samples, dried and of field moisture condition, respectively, were extracted by 0.01M calcium chloride (CaCl₂) at two different soil:extractant ratios (1:2 and 1:10), and analysed by inductively coupled plasma emission spectrometry (ICP) for content of P. The plant samples were digested in concentrated nitric acid (HNO₃) and the P content determined by ICP. Calcium chloride‐extractable P content was lowest in the middle of the growing season, while plant P was highest in the beginning of the season. Phosphorus extracted by CaCl₂ solution was higher at a soil:extractant ratio of 1:10 than at 1:2, and also when drying the soil before extraction. A soil:extractant ratio of 1:2 minimizes the risk of coming too near the limit of determination. However, if organic soils are also to be included, a ratio of 1:10 has to be used in order not to have all the solution absorbed by some types of soils. The solution of ammonium lactate/acetic acid (AL) extracted nearly two powers of ten more P than CaCl₂ solution. There was a good relationship between the methods. If calcareous or very acid soils had been included, a less good relation would have been expected. Plant P content varied more in straw than in grain between different treatments. Measuring CaCl₂‐extractable P with ICP might be able to predict plant uptake of P by plants. This would be a great advantage when using 0.01M CaCl₂ as a universal extradant.     

Evaluation of universal extractants for determining plant available potassium in intensively cultivated soils

Abstract

Eighteen soils from northwestern Switzerland were used to study the value of seven universal extractants (CaCl₂; DB‐DTPA; Mehlich 1, 2, and 3; Morgan‐Wolf; and NH₄OAc‐EDTA) for predicting plant available potassium (K) as compared to a bioassay (a modified Neubauer test with winter rye). These extractants were evaluated on the basis of K uptake by the bioassay test and the soil K status. In order to create the sufficiency level of exchangeable K for plant growth, soils were treated with 0, 20, 40, 80, and 160 mg K/kg of soil. The range of K uptake by the bioassay tests was between 89.2 and 403.0 mg/kg of soil for the control pots, and 136.6 to 495.8 for the K treatments with optimal conditions for plant growth. The average amounts of K extracted by the seven universal extractants, in ascending order, were: CaCl₂ < Morgan‐Wolf < Mehlich 1 < Mehlich 2 < NH₄OAc‐EDTA < Mehlich 3 < DB‐DTPA. The highest simple correlation with K uptake versus the bioassay test was obtained with the DB‐DTPA (r = 0.89) extractant and the lowest with the Mehlich 1 (r = 0.53) extractant. The DP‐DTPA, NH₄OAc‐EDTA and Mehlich 3‐K procedures showed an advantage over K procedures based on water soluble and exchangeable K pools in the investigated soils in order to predict the amount of plant‐available K. A simple regression and the Cate‐Nelson graphic method offer the possibility of assessing the soil‐K status using K values obtained by these universal extractants and to calibrate them against K forms as follows: exchangeable, water soluble, and non‐exchangeable.     

Sulfur mineralization in sphagnum peat

Abstract

Open and closed incubation systems were studied as means of quantifying sulfate fractions in sphagnum peat moss. Sulfate was extracted in the closed system with a 0.15% CaCl₂‐H₂O or a 500 mg P/L extractant. Sulfate was extracted in the open system with 10 mM KC1, 0.15% , CaCl₂‐H₂O, or 500 mg P/L extractant. Extractants were quantified by ion chromatography. Phosphate extractant released more sulfate than CaCl₂, in the closed system. There was a significant increase over time of sulfate released by the CaCl₂ extractant. In the open system, there was no significant difference in release and total amounts leached of sulfate‐S between extractants. The closed system released more sulfate‐S than the open system. Phosphate extractants in both systems mineralized 43% of initial sulfur content     

Extraction of water‐soluble organic matter from mineral horizons of forest soils

Dissolved organic matter (DOM) is involved in many important biogeochemical processes in soil. As its collection is laborious, very often water‐soluble organic matter (WSOM) obtained by extracting organic or mineral soil horizons with a dilute salt solution has been used as a substitute of DOM. We extracted WSOM (measured as water‐soluble organic C, WSOC) from seven mineral horizons of three forest soils from North‐Rhine Westphalia, Germany, with demineralized H₂O, 0.01 M CaCl₂, and 0.5 M K₂SO₄. We investigated the quantitative and qualitative effects of the extractants on WSOM and compared it with DOM collected with ceramic suction cups from the same horizons. The amounts of WSOC extracted differed significantly between both the extractants and the horizons. With two exceptions, K₂SO₄ extracted the largest amounts of WSOC (up to 126 mg C kg^–1) followed by H₂O followed by CaCl₂. The H₂O extracts revealed by far the highest molar UV absorptivities at 254 nm (up to 5834 L mol^–1 cm^–1) compared to the salt solutions which is attributed to solubilization of highly aromatic compounds. The amounts of WSOC extracted did not depend on the amounts of Fe and Al oxides as well as on soil organic C and pH. Water‐soluble organic matter extracted by K₂SO₄ bore the largest similarity to DOM due to relatively analogue molar absorptivities. Therefore, we recommend to use this extractant when trying to obtain a substitute for DOM, but as WSOM extraction is a rate‐limited process, the suitability of extraction procedures to obtain a surrogate of DOM remains ambiguous.     

Vergleich verschiedener Extraktionsmethoden zur Bestimmung der Kaliumverfügbarkeit in Böden

Comparison of different methods for the determination of the potassium availability of soils Extractable K was determined in 148 soil samples by using three different lactate solutions (AL, DL, CAL), 0.1 m HCl and 0.0125 m CaCl₂ as extracting agents. The extractable portion of the total exchangeable K (K(NH₄)) was found to decrease with increasing content of the < 6,3 μm particle size fraction in the samples. Correlation coefficients were calculated for characterizing the relationship between extracted amounts of K (K values) and the ?K numbers”?. The latter serve as a basis for fertilizer recommendations in the Netherlands, where they have been checked in a great number of field trials. The K number depicts the K supplying power of soils as determined by HCl soluble K, content of the < 16 μm size fraction, and pH. The K (CaCl₂) values were found to correlate more closely with the K numbers than the amounts of K extracted with lactate solutions. This is because the influence of particle size on K(CaCl₂) is eliminated as shown by multiple regression analysis. The strength of bonding of the easily exchangeable K is reflected much better by the K(CaCl₂) values than by the lactate values. Improvement of K fertilizer recommendations by taking K(CaCl₂) data as a basis can thus be expected. The different methods of recommendation for K fertilization in the Fed. Republic of Germany and in the Netherlands are illustrated for the soils derived from loess.     

Comparison of soil zinc extractants for detection of applied zinc and prediction of leaf zinc concentration

Abstract

Many soil extractants have been developed for determination of zinc (Zn) availability to plants. The optimum soil Zn extractant should be useful not only for prediction of plant Zn concentration but also for detection of applied Zn levels. The objectives of this study were: i) to compare soil Zn extradants for detecting applied Zn and for predicting peanut leaf Zn over a range of soil pH levels, and ii) to correlate other soil‐extractable Zn levels with Mehlich‐1. Soil and peanut leaf samples were taken from a field study testing pH levels as the main plots and Zn application rates in the sub‐plots. Extractable Zn was determined on soil samples using Mehlich‐1, Mehlich‐3, DTPA, MgNO₃, and many dilute salt extradants of varied strength and pH. Correlation of extractable soil Zn to cumulative applied Zn levels revealed Mehlich‐1, Mehlich‐3, DTPA, and AlCl₃ extradants to be among the best indicators of applied Zn. Leaf Zn concentration was best correlated with soil Zn extracted by dilute salts, such as KCl, CaCl₂, NH₄Cl, CaSO₄, and MgCl₂. Including soil pH as an independent variable in the regression to predict leaf Zn considerably improved R‐square values. The DTPA‐extractable soil Zn levels were very well correlated with Mehlich‐1‐extractable Zn. Mehlich‐3 extracted about 20% more soil Zn than Mehlich‐1, but Mehlich‐3 soil Zn was not as well correlated to Mehlich‐1 soil Zn as DTPA soil Zn. Lower pH solutions extracted more of the applied Zn, but more neutral solutions extracted Zn amounts which were better correlated with Zn uptake. On the other hand, Mehlich‐1, which had a lower pH, had better correlations with both applied Zn and leaf Zn than did Mehlich‐3. Shortening the DTPA extraction time to 30 minutes resulted in better correlations than the standard two hour extraction time. Chloride (Cl) was the best anion tested in relation to soil applied Zn recovery in combination with potassium (K), calcium (Ca), and aluminum (Al), and Cl optimized leaf Zn correlations for ammonium (NH₄), K, Ca, and magnesium (Mg). The larger the valence of the cation, the better the correlation with applied Zn and the poorer the correlation with leaf Zn.     

Optimization of DTPA and calcium chloride extractants for assessing extractable metal fraction in polluted soils

Abstract

Metal availability in soils is often assessed by means of extraction with chemical solutions, among others the chelating agent DTPA (diethylenetriaminepentaacetic acid) and the non‐buffered salt calcium chloride (CaCl₂). The same procedures are used for polluted soils that were originally created to assess the nutrient status of arable soils. We studied the influence of various parameters (type of shaker, shaking time, soil to solution ratio, and concentration of chemical extractant) and modify the DTPA and CaCl₂ extraction procedures to make them suitable for the study of polluted soils. The chosen extraction ratio and extractant concentration were the followings: 8 g/20 mL of 0.1 MCaCl₂ and 2 g/20 mL of 0.005 M DTPA. The optimized procedures were applied to nine soil samples affected by different sources of pollution (mine works, vehicle emissions, and various industries). Cadmium (Cd) showed the highest extractability with both extractants. Depending on the soil, copper (Cu) and zinc (Zn) (using DPTA) and Cu and manganese (Mn) (using CaCl₂) were the followings in the extractable amounts. Cadmium, Cu, and Zn were highly correlated in both extractions and with total contents.     

Evaluation of extractants for predicting availability of sulphur to mustard in inceptisols

Abstract

Mustard (Brassica juncea) is an important oilseed crop of northern India, which is widely grown in Delhi and adjoining States. This crop has a relatively high requirement of sulphur (S), and is sensitive to S‐deficiency. For predicting response of mustard to S application, several extractants have been tried with variable results. Since selection of a promising extractant for a particular soil needs careful consideration, the present investigation was planned to select the most promising extractant to predict the availability of S to mustard grown on Inceptisols of Delhi. For this purpose, a greenhouse experiment was conducted with twenty soils (two from each often important soil series from the cultivated alluvial soil belt of Delhi. Nine extractants, commonly used for estimating the availability of S, were evaluated and S in soil extract and in plant digest was estimated using the turbiditimetric method. The results indicate that the phosphate salt methods extracted comparatively more S than other extractants. The amount of S extracted by these extractants was found in the following order: KH₂PO₄‐500 ppm P>Ca(H₂PO₄)₂‐500 ppm P>0.001 M HCl>NaOAc+HOAc>heat soluble S>0.15% CaCl₂>l% NaCl> water soluble S>NH₄OAc+HOAc. Simple correlation coefficients of the amounts of S extracted by different extractants and the forms of S with the plant parameters were worked out. To determine the combined effect of soil characteristics on S extraction by different extractants, stepwise multiple regression analysis was carried out. Based on this study, the suitability of the extractants for mustard crops in Inceptisols of Delhi may be arranged as follows: 0.15% CaCl₂>water soluble S>0.001 M HCl>Ca(H₂PO₄)₂‐500 ppm>1%NaCl>NH₄OAc+HOAc>NaOAc+HOAc>KH₂PO₄‐500 ppm P>heat soluble S.     

Effects of moist storage and different drying temperatures on the extractability of iron,copper, manganese,and zinc in soil samples

Abstract

The objective of this study was to investigate the effect of different pretreatments on the extraction of cationic micronutrients [iron (Fe), copper (Cu), manganese (Mn), and zinc (Zn)] from four different soils. Samples were either stored in the field‐moist state for seven days before drying or dried immediately. Three drying treatments were used: air‐dried (72 hours), oven‐dried at 40°C (48 hours), or oven‐dried at 105°C (24 hours). Micronutrients were then extracted with 0.1N HC1 or diethenetriamine‐pentacetic acid (DTPA). Storage, drying temperature, extractant, and soil type all influenced micronutrient extractability. In general, a higher temperature increased the level of micronutrient extracted. However, the reverse effect was also observed. The effect of storage was variable and probably depended on the sample moisture content. We conclude that the results from routine analysis and experimentally determined indices can only be compared if soil samples are subjected to the same pretreatments. Hence, rigorous standardization of the sample preparations is imperative for accurate determination of plant‐available micronutrients.     

Comparison of mehlich 3, mehlich 1, ammonium bicarbonate‐DTPA, 1.0M ammonium acetate,and 0.2M ammonium chloride for extraction of calcium,magnesium, phosphorus,and potassium for a wide range of soils

Abstract

Extractants employed for routine soil analysis vary from one laboratory to another. Lack of a universal soil extractant is a serious limitation for interpretation of analytical results from various laboratories on nutritional status of a given soil. This limitation can be overcome by developing functional relationships for concentrations of a given nutrient extractable by various extradants. In this study, extractability of Ca, Mg, P, and K in a wide range of soils (0–15 cm) from citrus groves in Florida representing 21 soil series, with varying cultural operations, were compared using Mehlich 3 (M3), Mehlich 1 (M1), ammonium acetate (NH₄AOc), pH = 7.0 (AA), 0.2M ammonium chloride (NH₄Cl), and ammonium bicarbonate‐DTPA (AB‐DTPA) extractants. Soil pH (0.01M CaCl₂) varied from 3.57 to 7.28. The concentrations of Ca or Mg extractable by M3, M1, AA, and NH₄Cl were strongly correlated with soil pH (r² = 0.381–0.482). Weak but significant correlations were also found between AB‐DTPA extractable Ca or Mg and soil pH (r² = 0.235–0.278). Soil pH relationships with extractable K were rather weak (r² = < 0.131) for M1 and NH₄Cl but non‐significant for M3, AB‐DTPA, and AA. Concentrations of Ca, Mg, and K extractable by M3 were significantly correlated with those by either M1, AA, or NH₄Cl extractants. Mehlich 3‐P was significantly correlated with P extractable by M1 extractant only. Mehlich 3 versus AB‐DTPA relationship was strong for K (r² = 0.964), weaker for Mg and P (r² = 0.180–0.319), and non‐significant for Ca. With the increasing emphasis on possible use of M3 as an universal soil extractant, data from this study support the hypothesis that M3 can be adapted as a suitable extractant for routine soil analysis.     

Evaluation of Soil Tests for Plant‐available Mercury in a Soil–Crop Rotation System

A reliable soil test is needed for estimating mercury (Hg) availability to crop plants. In this study, four extraction procedures including 0.1 M hydrochloric acid (HCl), 1 M ammonium acetate (NH₄OAc) (pH 7.0), 0.005 M diethylenetriaminepentaacetic acid (DTPA), and 0.1 M calcium chloride (CaCl₂) (pH5.0) were compared for their adequacy in predicting soil Hg availability to crop plants of a rice–cabbage–radish rotation system. The amounts of Hg extracted by each of the four procedures increased with increasing equilibrium time. The optimal time required for extraction of soil Hg was approximately 30 min, though it varied slightly among the four extractants. The amounts of Hg extracted decreased with increasing soil/solution ratio, and a soil/solution ratio of 1:5 appeared to be adequate for soil Hg availability tests. The amounts of Hg extracted increased in the order of NH₄OAc < CaCl₂ < DTPA < HCl in silty loam soil (SLS) soil, and the order was NH₄OAc < CaCl₂ ≈ DTPA < HCl in yellowish red soil (YRS) soil. Significant positive correlations among the four extractants were obtained in SLS soil. In contrast, the correlations were poor in YRS soil, especially for HCl. There were significant correlations between concentrations of Hg in edible tissue of three plants and the amounts of soil Hg extractable to the four extractants for soil–rice system and soil–radish system, but not for soil–Chinese cabbage system. The 0.1M HCl extraction overall provided the best estimation of soil‐available Hg and could be used to predict phytoavailability of Hg in soil–crop systems.     

Evaluation of soil sulfate extractants and methods of analysis for plant available sulfur

Abstract

A steady decline in sulfur additions to Atlantic Canadian soils has prompted the need for an accurate method of determining their plant available sulfur status. Three soils were extracted with five soil extractants ‐ 0.01M Ca(H2PO₄)₂‐H₂O in 2M HOAc, 0.1M CaCl₂, Bray‐1 and de‐ionized water. The soil extracts were analyzed for sulfur or sulfate using inductively coupled argon plasma emission spectrometry (ICAP), AutoAnalyzer (AAN), anion exchange‐high performance liquid chromatography (HPLC‐CD) or atomic absorption spectroscopy (AAS). Results were compared with plant response of sulfur treatments to red clover, ryegrass, canola and wheat in a growth room. Instrument reproducibility and crop response indicated the ideal method of determining plant available soil sulfur was HPLC‐CD using the extractant Ca(H2PO₄)₂‐H₂O.     

Assessment of Suitable Extractants for Predicting Plant-available Potassium in Indian Coastal Soils

The suitability of seven chemical extractants was evaluated on 24 Indian coastal soils for prediction of plant-available potassium (K) to rice (Oryza sativa L. var. NC 492) grown in modified Neubauer technique. Average amounts of soil K extracted were in descending order: 0.5 M NaHCO₃ > neutral 1 N NH₄OAc > 0.02 M CaCl₂ > Bray and Kurtz No.1 > 1 N HNO₃ > 0.1 N HNO₃ > distilled water. The highest simple correlation with plant K uptake was obtained with 0.1 N HNO₃-K (r = 0.848) and lowest with CaCl₂-K (r = 0.805). Predictive models were developed using plant K uptake as the dependent variable and extractable soil K, sand, silt, soil pH, and electrical conductivity as the independent variables. Based on the final R² and ease of measurement, distilled water, 1 N NH₄OAc, and 0.1 N HNO₃ models were the best predictors of plant-available K in coastal soils when used along with sand or soil pH.     

Extraction of potassium from some kaolinitic soils of the tropics

Abstract

Three methods for soil potassium extraction (M NH₄OAc pH 7, 0.01 M AgTU and 30 % hot H₂SO₄) were compared for a variety of kaolinitic soils of the tropics. The AgTU‐extractable K was much higher than the M NH₄OAc‐extractable K when vermiculite clay was present in the soil. The correlation between both was given by an R value of 0.937. The amounts of K extracted by 0.01 M AgTU and by hot H₂SO₄ were approximately the same. The R value for these two methods was 0.843.

It is suggested that the AgTU extractant could be used for determination of plant‐available K in soil and for testing for the presence or absence of vermiculite clay in soils.     

Soil micronutrient contents and relation to other soil properties in Ethiopia

Abstract

Alfisols, Vertisols, Inceptisols, Aridisols, Mollisols, and Entisols were sampled (0–30 cm) from 32 locations across Ethiopia. The soils were analyzed for copper (Cu), zinc (Zn), manganese (Mn), and iron (Fe) contents using 0.005 M diethylene triamine pentaacetic acid (DTPA), 0.05 M hydrochloric acid (HC1), and 0.02 M ethylene diamine tetraacetic acid (EDTA) extractants. EDTA extracted more of each micronutrient than DTPA, which extracted greater amounts than HC1. The quantities of EDTA and DTPA‐extractable micronutrients were significantly correlated, and were in the order: Mn>Fe>Cu>Zn. The order of HCl‐extractable micronutrients was Mn>Fe>Zn>Cu. Micronutrient contents of Mollisols, Vertisols, and Alfisols were usually greater than those of the other soils, and Entisols usually had the lowest micronutrient contents. The contents were mostly positively correlated with clay and Fe₂O₃ contents, but negatively correlated with soil pH and A1₂O₃contents. While comparison of DTPA‐ and EDTA‐extractable micronutrients with critical levels showed that most soils had adequate amounts of the micronutrients for crops, the amounts extracted by HC1 were below critical levels in most soils. Since the critical levels that were used in the comparisons were not established in Ethiopia, calibration of the soil contents of these micronutrients with crops grown in Ethiopia is required to identify the most suitable extractant(s).     

Addition of phosphorus to soils with low to medium phosphorus retention capacities. II. effect on soil phosphorus extractability

Abstract

Knowledge of the change in soil extractable phosphorus (P) as a consequence of soil P fertilization could be useful in discriminating soils with a potential for soil P release to runoff or movement of P along the soil profile. In this research, soils with low to medium P retention capacity were equilibrated for 90 days with soluble P (KH₂PO₄) at rate of 100 mg P kg^‐1 soil. After this period, soil samples both with and without the P addition were analyzed using six conventional methods: 1) Olsen, 2) Bray 1,3) Mehlich3,4) Egner, 5) Houba, dilute CaCl₂ solution, and 6) distilled water, and three “innovative”; P‐sink methodologies: 1) Fe oxide‐coated paper strip, 2) anion exchange resin membrane, and 3) cation‐anion exchange resin membrane. The soils without P addition had low levels of extracted P as determined by all nine procedures. Net increases in the amount of P extracted from the soils with added P ranged from 4.2 mg kg^‐1 (CaCl₂ extraction) to 57.6 mg kg^‐1 (cation‐anion resin membrane extraction). Relationships between change in extracted P and i) physical and chemical characteristics, and ii) soil P sorption properties are also presented and discussed.     

Methods of assessing boron availability to kiwifruit plants growing on high boron soils

Abstract

Five soil boron (B) extraction methods were evaluated for their ability to predict available B to kiwifruit plants in soils with high B concentration. The methods were hot water soluble (Hws‐B), 0.05M mannitol in 0.01M calcium chloride (CaCl₂ extractable (Man‐B), 0.05M hydrochloride acid (HCl) soluble (HC1‐B), resin extractable (Resin‐B), and saturation extract (Sat‐B). The amounts of B recovered by the first four methods investigated were strongly correlated with each other, the highest correlation obtained being between Hws‐B and HC1‐B. Plant B was highly correlated to the B recovered by the first four extractants and poorly correlated to the B determined by the saturation method. Soil B concentrations corresponding with B toxicity in kiwifruit are 0.51, 0.80, 0.18, and 2.0 μg‐g^‐1 soil for Hws‐B, Man‐B, HC1‐B, and Res‐B, respectively. The coefficients of determination in some cases were improved when in the regression equations, soil pH and clay content were included.     

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.     

Available Nitrogen for Corn and Winter Cereal in Spanish Soils Measured by Electro‐ultrafiltration,Calcium Chloride,and Incubation Methods

Abstract

Comparison of methods is necessary to develop a quick and reliable test that can be used to determine soil‐available nitrogen (N) in an attempt to increase the efficiency of N fertilizers and reduce losses. The objectives of this research were to compare the fractions extracted by the calcium chloride (CaCl₂) and the electro‐ultrafiltration (EUF) methods and to correlate them to the mineralization rate (k) obtained from a 112‐d incubation of 61 soil samples. Thirty‐five soil samples were collected from cornfields and 26 from winter cereal fields. Subsamples were either aerobically incubated to calculate k or extracted by the EUF and CaCl₂ methods to identify three fractions: nitrate (NO₃ ^?)‐N, ammonium (NH₄ ⁺)‐N, and Norg‐N. The Norg‐N extracted by both methods was larger in soils from cornfields than in soils from winter cereal fields. In samples from cornfields, the Norg‐N fraction obtained by the EUF method was correlated to the Norg‐N measured by the CaCl₂ method (r=0.46). Soil N content was related to k in samples from cornfields (r=0.40) but not in samples from winter cereal fields. Also, k was correlated to inorganic N content extracted by both chemical methods. The CaCl₂ method was a reliable alternative for laboratories to determine soil‐available N for corn but not for winter cereal.     

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.