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 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.     

Comparison of Mehlich-3 and Ammonium Bicarbonate-DTPA for the Extraction of Phosphorus and Potassium in Calcareous Soils from Florida

Developing a fast and reliable soil testing method is critical for improving soil testing efficiency and ensuring reliable fertilizer recommendation. The objectives of this study were to evaluate Mehlich-3 (M-3) as a replacement for ammonium bicarbonate-diethylenetriaminepentaacetic acid (AB-DTPA) to extract phosphorus (P) and potassium (K) and to determinate the relationships between extractable P and K and their uptakes by crop in calcareous soils. M-3 and AB-DTPA were compared by using two approaches. In the first approach, the amounts of extracted P and K were compared by analyzing soil samples collected from agricultural production areas; in the second approach, snap beans (Phaseolus vulgaris) were grown in pot to determine the P and K uptakes by crop. There were significant correlations between M-3 and AB-DTPA for both soil test P and K based on soils collected from the agricultural field and the pot study. Soil test P and K by both extractants were significantly correlated with their uptakes by snap bean. The critical value of M-3-P regarding snap bean uptake was 47 mg kg^?1 and was higher than that (18 mg kg^?1) for AB-DTPA-P, whereas critical soil test K levels were similar between M-3 and AB-DTPA. M-3 was identified as an alternate improved extraction method instead of AB-DTPA in calcareous soils based on this study. However, more work will be needed to identify the correlation of the two extractants and crop responses under a field condition.     

Combination of Different Extractants to Assess Binding Forms of Some Elements in Soil Profiles

Abstract

Three different chemical extractants were evaluated as to their extraction efficiency for copper (Cu), zinc (Zn), lead (Pb), aluminium (Al), iron (Fe), chromium (Cr), manganese (Mn), potassium (K), magnesium (Mg), and calcium (Ca) on forest soil profiles from the Romanian Carpathians. The extractants were hot 14 M nitric acid (HNO₃), 0.05 M hydrochloric acid (HCl), and 0.1 M sodium pyrophosphate. By comparing amounts extracted by 0.05 M HCl and 0.1 M sodium pyrophosphate relative to that dissolved by hot 14 M HNO₃, some conclusions were drawn concerning the chemical forms of the metals in the extractable pool. The amount released by 0.05 M HCl was generally less than 10% of the HNO₃‐extractable fraction but showed considerable variation among the elements studied. The relative amount extracted by pyrophosphate increased with organic‐matter content of the soils for Cu, Zn, Pb, Al, Fe, and Cr; stayed more or less constant for Mn, K, and Mg; and decreased for Ca. These findings are discussed with respect to the different binding forms of the metals in the soil and the processes affecting their mobility. From the present results, the metals were ranked as follows with respect to their ability to form organic complexes in natural soils: Cu>Cr, Pb>Ca>Al>Fe, Zn, Mn, K>Mg. However, the use of cold dilute HCl as a fractionation step may be questionable in cases of soils with a high content of substances possessing large neutralization capacity for protons.     

Mineralogical budgeting of potassium in soil: A basis for understanding standard measures of reserve potassium

The study was conducted to investigate the relationship between some standard measures of soil reserve potassium (K) and soil mineralogy. Eight different agricultural soils from the N temperate and S boreal regions were studied and analyzed both by standard methods (exchangeable K, 2 M HCl‐ and aqua regia–extractable K) and by quantitative mineralogical methods based on X‐ray powder diffraction analysis of spray‐dried bulk soils. Linear regression and multivariate methods were used to assess the relationships between standard measures of soil reserve K and a number of soil chemical, physical, and mineralogical properties. A mineralogical budgeting approach, to estimate total K and its speciation between different mineral phases, is shown to be accurate after validation against total K analyzed geochemically. This approach enabled us to determine that both HCl‐ and aqua regia–extractable K were highly correlated with K in dioctahedral phyllosilicates and extracted 1%–17% and 5%–45% of total K, respectively. Neither extraction showed any obvious relationship to K in feldspar, which is frequently a larger reservoir of K in the soils examined.     

Evaluation of Universal Extractants for Determination of Some Macronutrients from Soil

Evaluation of nutrient status in soil is important for nutritional, environmental, and economical aspects. The objective of this work was to find out the most suitable universal extractant for determination of available phosphorus (P) and nitrate (NO₃-) and exchangeable potassium (K), calcium (Ca), and magnesium (Mg) from soils using 0.01 M calcium chloride (CaCl₂), 0.01 M barium chloride (BaCl₂), 0.1 M BaCl₂, 0.02 M strontium chloride (SrCl₂), Mehlich 3, and ammonium bicarbonate diethylene triamine penta acetic acid (AB-DTPA) extractants. Composite surface soil samples (0–20 cm) were collected from the Eastern Harage Zone (Babile and Haramaya Districts), Wolaita Zone (Damot Sore, Boloso Bombe, Damot Pulasa, and Humbo Districts), and Dire Dawa Administrative Council by purposive sampling. The experiment was carried out in a completely randomized design (CRD) with three replications. Results indicated that the greatest correlations were found between Mehlich 3 and Olsen method and also between 0.02 M SrCl₂ and Olsen method for available P. The amount of NO₃^– extracted by 0.02 M SrCl₂ was significantly correlated to the amount determined by 0.5 M potassium sulfate (K₂SO₄). The amounts of exchangeable K, Ca, and Mg determined by ammonium acetate (NH₄OAc) method were significantly correlated to the amount determined by universal extractants tested. In general, both 0.02 M SrCl₂ and Mehlich 3 can serve as universal extractants for the macronutrients considered in this study with the former being more economical when NO₃^– is included.     

Potassium fixation capacity of some highly calcareous soils as a function of clay minerals and alternately wetting-drying

ABSTRACT

The current research was done to investigate the effect of wetting-drying cycles, time, and clay mineralogy on K fixation capacity of highly calcareous soils. In order to conduct the study, eight soil samples were collected. The samples were treated with different concentrations of K including 200 (K1), 400 (K2) and 800 mg kg^?1 (K3) and 8 different incubation time including 6 h (t1), 24 h (t2), 72 h (t3), one week (t4), two weeks (t5), one month (t6), two months (t7) and three months (t8). Also, a wetting-drying treatment was done (td) in order to simulate the effect of irrigation and soil drying on K fixation. The results showed that for all K levels addition, the percentage of fixed K was increased with time. The K fixation content was increased with the increase in the added K from K1 to K3, while K fixation percentage was decreased. The results also showed that there was a significant difference between soils with wetting-drying treatment (td) and soils with three-month incubation (t8) in K fixation capacity, so that the fixation of K by the soils was increased with wetting-drying cycles.     

Experimental Evaluation of Procedures to Quantify Carbohydrate Carbon in Some Calcareous Soils

Carbohydrates are an important component of soil organic matter, and a method is needed to quantify them, which would be efficient in terms of time and cost. Different extractants and methods were examined in this work for their efficiency to extract carbohydrate C from four calcareous soils. Four extractants (distilled water, 0.5 M potassium sulfate (K₂SO₄), and 0.25 and 0.5 M sulfuric acid (H₂SO₄)) and three incubation methods (shaking for 16 h, heating in an oven (85 °C) for 16 h, and heating in a water bath (85 °C) for 2.5 h) were compared. The results show that significantly more carbohydrate C was extracted from all four soils with oven and water bath heating of the soil–extractant suspensions than with shaking them at room temperature. The efficiency of the extractants decreased in this order: 0.5 M H₂SO₄ > 0.25 M H₂SO₄ > 0.5 M K₂SO₄. The combination of the heated–water bath incubation method with 0.5 M H₂SO₄ as extractant was the most efficient method.     

Evaluation of Chemical Extractants for the Determination of Available Potassium

Abstract

Evaluation of nutrient status in soil is important for nutritional, environmental, and economical aspects. This research was carried out to determine the potassium (K) available to corn (Zea mays) in 15 soils from the Hamedan province in the west of Iran. The treatments included two K levels [0 and 200 mg K kg^?1 as potassium sulfate (K₂So₄)] and 15 soils in a factorial experiment in a randomized block design with three replications. The results indicated that K application increased yield, K concentration, and K uptake of corn. According to the mechanism of the extraction, these extractants can be classified into four groups. The first group of extractants, acidic extractants, includes 0.02 M strontium chloride (SrCl₂)+0.05 M citric acid, 0.1 M hydrochloric acid (HCl), and Mehlich 1. The second group includes 0.1 M barium chloride (BaCl₂), 0.01 M calcium chloride (CaCl₂), and 1 M sodium acetate (NaOAc). The third group includes 1 M ammonium acetate (NH₄OAc), ammonium bicarbonate–diethylenetriamine tetraacetic acid (AB‐DTPA), and finally distilled water. The results showed that correlation between extractants in each groups were significantly high. Correlation studies showed that NH₄OAc and AB‐DTPA cannot be used as available K extractants. The correlation of other extractants with relative yield, plant response, and K uptake were significantly high. Therefore, these extracting solutions can be used as available K extractants.

Potassium critical levels by extractants were also determined using the method by Cate and Nelson (1971) Cate, R. B. and Nelson, L. A. 1971. A simple statistical procedure for partitioning soil test correlation into two classes. Soil Science Society of America Proceeding, 35: 658–660. [Crossref], [Web of Science ®] , [Google Scholar]. Potassium critical levels for 90% relative yield were 29, 27, 82, 84, 45, 145, and 272 mg kg^?1 for 0.002 M SrCl₂, distilled water, 0.02 M SrCl₂+0.05 M citric acid, 0.1 M HCl, Mehlich 1, 1 M NaOAC, and 0.1 M BaCl₂, respectively.     

Suitability of Different Soil Extractants for Determination of Available Cu and Mn Contents in Polish Soils

The aim of this study was to compare four micronutrient soil-test extractants currently in common use in Poland, Rinkis, Mehlich 3, modified Lindsay and Norvell, and Yanai, for ability to determine the plant-available concentration of copper (Cu) and manganese (Mn) in two acidic soils (pH 4.8–4.9) that had been amended with different doses of Cu and Mn fertilizers. The comparison was based on two pot experiments (each with a different soil) with corn (Zea mays), barley (Hordeum vulgare), spring wheat (Triticum aestivum), rape (Brassica napus), red clover (Trifolium pratense), and English ryegrass (Lolium perenne). The extractants were evaluated based on a correlation analysis of the microelement concentrations in plants at the end of the vegetative phase and micronutrient concentration in the fertilized soil determined by each extractant at the end of the experimental period. The largest extractable concentrations of Cu and Mn in soils were obtained with Rinkis. The modified Lindsay and Norvell soil test extracted the lowest amount of both microelements. For soil Cu, the results with the Mehlich 3 and Yanai extractants were highly correlated with the Rinkis procedure results (r = 0.98). The modified Lindsay and Norvell results were not as well correlated with Rinkis (r = 0.84). For soil Mn, the correlation of results of Yanai, Mehlich 3, and modified Lindsay and Norvell to Rinkis ranged from r = 0.80 to r = 0.86. Levels of Mn and Cu measured with each of the extractants were highly correlated with plant tissue concentrations of Mn and Cu in most of the six plant species. The exceptions to this were the following: The modified Lindsay and Norvell soil Cu levels were not correlated with ryegrass and wheat plant Cu levels; Mehlich 3 Cu was not correlated with red clover Cu; and the Rinkis-extractable Mn was not correlated with the wheat Mn. It is concluded that the Yanai and Mehlich 3 procedures are suitable alternatives to the Rinkis for Cu but not for Mn.     

Potassium Fixation and Release Characteristics of Some Benchmark Soil Series under Rice–Wheat Cropping System in the Indo‐Gangetic Plains of Northwestern India

Abstract

Potassium (K) fixation and release in soil are important issues in long‐term sustainability of a cropping system. Fixation and release behavior of potassium were studied in the surface and subsurface horizons in five benchmark soil series, viz. Dhar, Gurdaspur, Naura, Ladowal, and Nabha, under rice–wheat cropping system in the Indo‐Gangetic plains of India. Potassium fixation was noted by adding six rates of K varying from 0 to 500 mg kg^?1 soil in plastic beakers while K release characteristics were studied by repeated extractions with 1 M HNO₃ and 1 M NH₄OAc extractants. The initial status of K was satisfactory to adequate. Potassium fixation of added K increased with the rate of added K irrespective of soil mineralogy and soil depth. Soils rich in K (Ladowal and Nabha) fixed lower amounts (18–42%) of added K as compared to Gurdaspur, Dhar, and Naura (44.6–86.4%) soils low in K. The unit fertilizer requirement for unit increase in available K was more in low‐K soils. The study highlights the need for more studies on K fixation in relation to the associated minerals in a particular soil. Potassium‐release parameters such as total extractable K, total step K, and CR‐K varied widely in different soil series, indicating wide variation in the K‐supplying capacity of these soils. K released with 1 M NH₄OAc extractant was 20–33% of that obtained with 1 M HNO₃. Total extractable K using 1 M HNO₃ varied from 213 to 528 mg kg^?1 and NH₄OAc‐extractable K ranged from 71 to 312 mg kg^?1 soil in surface and subsurface layers of different soil series. The Ladowal and Nabha series showed higher rates of K release than Gurdaspur, Dhar, and Naura series, indicating their greater K‐supplying capacity.     

Divergent Relationships of Phosphorus Soil Tests in Temperate Grassland Soils

Abstract

Various soil tests are used to estimate phosphorus (P) availability for both crop uptake and potential loss to water. Conversion equations may provide a basis for comparison between different tests and regions, although the extent to which information can be interchanged is uncertain. The objective was to determine and quantify relationships between specific soil test extractants for samples taken annually in October and February over 4 years from four sites in each of eight soil series under grassland. The extractants comprised Mehlich‐3, Morgan, Olsen, Bray‐1, lactate–acetate, CaCl₂ (1∶2 and 1∶10 soil–solution ratios), and resin. The results showed distinct relationships for each soil series, for which individual lines regression models (different intercepts and slopes) were superior to a single conversion equation across all soils. The ensuing difference between soils was large and ranged from 1.9 to 8.0 and 9.2 to 15.6 mg kg^?1 P for Morgan and Olsen, respectively, at 20 mg kg^?1 Mehlich‐3 P. Generally, the environmentally oriented tests CaCl₂ and resin correlated best with Morgan. Some soil‐specific limitations were also observed. CaCl₂ was less efficient than Morgan, and Morgan less efficient than Mehlich‐3 on a high Fe–P soil derived from Ordovician‐shale diamicton, compared with the general trend for other soils. This finding suggests that further disparity may arise where evaluation of critical, or other, limits across regions involves even a limited sequence of tests.     

Evaluation of Extractants and Quantity–Intensity Relationship for Estimation of Available Potassium in Some Calcareous Soils of Western Iran

Accurate estimation of the available potassium (K⁺) supplied by calcareous soils in arid and semi‐arid regions is becoming more important. Exchangeable K⁺, determined by ammonium acetate (NH₄OAc), might not be the best predictor of the soil K⁺ available to crops in soils containing micaceous minerals. The effectiveness of different extraction methods for the prediction of K‐supplying capacities and quantity–intensity relationships was studied in 10 calcareous soils in western Iran. Total K⁺ uptake by wheat grown in the greenhouse was used to measure plant‐available soil K⁺. The following methods extracted increasingly higher average amounts of soil K⁺: 0.025 M H₂SO₄ (45 mg K⁺ kg^?1), 1 M NaCl (92 mg K⁺ kg^?1), 0.01 M CaCl₂ (104 mg K⁺ kg^?1), 0.1 M BaCl₂ (126 mg K⁺ kg^?1), and 1 M NH₄OAc (312 mg K⁺ kg^?1). Potassium extracted by 0.01 M CaCl₂, 1 M NaCl, 0.1 M BaCl₂, and 0.025 M H₂SO₄ showed higher correlation with K⁺ uptake by the crop (P < 0.01) than did NH₄OAc (P < 0.05), which is used to extract K⁺ in the soils of the studied area. There were significant correlations among exchangeable K⁺ adsorbed on the planar surfaces of soils (labile K⁺) and K⁺ plant uptake and K⁺ extracted by all extractants. It would appear that both 0.01 M CaCl₂ and 1 M NaCl extractants and labile K⁺ may provide the most useful prediction of K⁺ uptake by plants in these calcareous soils containing micaceous minerals.     

Effect of Grinding on Soil Extraction by Aqua Regia, 2 M Nitric Acid,and Mehlich 3

Abstract

The effect of grinding on soil extraction was determined for two soil fractions and three extractants. Arsenic (As), beryllium (Be), cadmium (Cd), cobalt (Co), chromium (Cr), copper (Cu), nickel (Ni), lead (Pb), vanadium (V), and zinc (Zn) were extracted by aqua regia and 2 M nitric acid. Mehlich 3 extractant was used for determination of potassium (K), magnesium (Mg), calcium (Ca), phosphorus (P), iron (Fe), and aluminum (Al). One hundred forty‐seven agricultural soil samples representing all major soil types, climatic regions, and proportions of agronomic cultures in the Czech Republic were collected for the study. Particle size fractions smaller than 2 mm and smaller than 0.150 mm were chosen for investigation. Extraction of elements by aqua regia was similar for both size fractions of soil. Cold 2 M nitric acid is a weaker extractant than aqua regia, and a statistically significant increase in extractable Be (5%), Cd (6%), Co (11%), Cu (5%), Ni (5%), and V (2%) was measured with the finely ground soils. An increase for the finer fraction for K (10%) and Mn (25%) was found for Mehlich 3. A more complex nonlinear relationship was found for Mehlich 3 extractable Al and Fe. This was probably caused by a more intensive re‐adsorption of Fe and Al to the finely ground soils.     

Development of a New Soil Extractant for Simultaneous Phosphorus,Ammonium, and Nitrate Analysis

Abstract

A new soil extractant (H³A) with the ability to extract NH₄, NO₃, and P from soil was developed and tested against 32 soils, which varied greatly in clay content, organic carbon (C), and soil pH. The extractant (H³A) eliminates the need for separate phosphorus (P) extractants for acid and calcareous soils and maintains the extract pH, on average, within one unit of the soil pH. The extractant is composed of organic root exudates, lithium citrate, and two synthetic chelators (DTPA, EDTA). The new soil extractant was tested against Mehlich 3, Olsen, and water for extractable P, and 1 M KCl and water‐extractable NH₄ and NO₂/NO₃. The pH of the extractant after adding soil, shaking, and filtration was measured for each soil sample (5 extractants×2 reps×32 soils=320 samples) and was shown to be highly influential on extractable P but has no effect on extractable NH₄ or NO₂/NO₃. H³A was highly correlated with soil‐extractable inorganic N (NH₄, NO₂/NO₃) from both water (r=0.98) and 1 M KCl (r=0.97), as well as being significantly correlated with water (r=0.71), Mehlich 3 (r=0.83), and Olsen (r=0.84) for extractable P.     

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.     

Soil Phosphorus Extracted by Bray 1 and Mehlich 3 Soil Tests as Affected by the Soil/Solution Ratio in Mollisols

Different relationships between soil-test methods results have been reported in several agricultural regions. Differences in the same soil-test procedure (e.g., soil/solution ratio) exist between soil-testing laboratories from different agricultural regions. Our objectives were to (1) determine the effect of soil/solution ratio on the amount of phosphorus removed by Bray 1 and Mehlich 3 methods, (2) compare the amounts of phosphorus removed by Bray 1 and Mehlich 3 in Mollisols from the Pampean region, and (3) determine whether soil/solution ratio affects the relationship between Bray 1 and Mehlich 3. Soil phosphorus availability was determined with two extractants (Bray 1 and Mehlich 3), using two soil/solution ratios (1:10 and 1:8, wt/v) in 72 soils (noncalcareous, loess-derived Molisolls) from the Pampean region. The amount of phosphorus removed was 20–24% greater when using 1:10 than 1:8 (wt/v) soil/solution ratio. This effect was significantly greater in Bray 1 than in Mehlich 3 (p = 0.04). When compared using the same soil/solution ratio, Mehlich 3 removed 4 to 8% more phosphorus than Bray 1. The soil/solution ratio used in the comparison affected the relationship between both extractants. The difference between extractants was slightly greater with a soil/solution ratio of 1:8 than of 1:10 (p = 0.03). Our results showed that even when using the same method, changes in the procedure (like soil/solution ratio) may cause different soil-test results and also differences in the relationship between two extracting solutions. Therefore, reported relationships between two methods are only valid for the soils and region where the relationship was developed and should not be extrapolated to other regions, even with similar soils.     

Different Fractions of Soil Potassium,Olsen Phosphorus,and Available Sulfur Status of Intensively Cultivated Berpura Soil Series of India and Nutrient Indexing of Rice Crop

Berpura alluvial soil series of the Indo‐Gangetic Plains is situated in the Ambala District of the Haryana State of India. Soils of this series had medium concentrations of both potassium (K) and phosphorus (P) and large concentrations of sulfur (S) before 1970. To study different fractions of K, Olsen P, and 0.15% calcium chloride (CaCl₂)–extractable (available) S of soils of the Berpura series and to create nutrient indexing of rice crops growing on this series, surface soil samples were collected from 100 farmers' fields after the harvest of the wheat crop in 2005. During kharif season of same year, samples of upper two leaves at anthesis growth stage of rice crop were also collected from the same 100 farmers' fields that had earlier been sampled for soil analysis. Analysis of soil samples showed more K depletion in soils of this series, of which 86% of farmers' fields were deficient in ammonium acetate (NH₄OAc) K (available K). Thirty and 62% of leaf samples of the rice crop growing on the 100 fields of this series were extremely and moderately deficient in K, respectively. The mean values of water‐soluble, exchangeable, nonexchangeable, lattice, and total K were 10.6, 30.3, 390.0, 8204, and 8635 mg kg^?1, respectively. In soils of this series, 0.123, 0.351, 4.517, and 95.009% of total K were found in water‐soluble, exchangeable, nonexchangeable, and lattice K forms, respectively. On the other hand, long‐term farmers' practice of more application of P fertilizer in wheat crop has resulted in P buildup in the soils of the Berpura series. Olsen P in soils of farmers' fields of this series ranged from 9.0 to 153.0 mg kg^?1, with the mean value of 41.8 mg kg^?1. Eighty‐two percent of leaf samples of rice crops grown on this series without application of P fertilizer were sufficient in P. The analysis of soil and rice crops for P and K proved the suitability of 0.5 M sodium bicarbonate (NaHCO₃) and 1 N NH₄OAc for extracting available P and K, respectively, in alluvial soils of the Indo‐Gangetic Plains. The 0.15% CaCl₂–extractable S in this soil ranged from 9.6 to 307 mg kg^?1 with a mean value of 34.6 mg kg^?1. Four and 26% of soil samples had low and medium, respectively, in 0.15% CaCl₂–extractable S. S deficiency was recorded in rice crops, as 29% of the leaf samples were extremely deficient in S and 58% were moderately deficient in S. This indicated the unsuitability of the 0.15% CaCl₂ to extract available S from the Udic ustochrept utilized for cultivation of rice crops.     

Phosphorus Fertilizer Calibration for Sugarcane on Everglades Histosols

A calibrated soil test for phosphorus (P) fertilizer application to sugarcane (Saccharum spp.) grown on organic soils in southern Florida is an important best-management practice for minimizing P loads in water draining to the Everglades. The current calibration uses water as the soil extractant, which has the limitations of being very sensitive to pH and being most applicable to short-season crops. Phosphorus fertilizer rate studies at six locations (20 total crop years) were analyzed to develop an updated soil-test P calibration for sugarcane on organic soils. Phosphorus extracted with water, acetic acid, and Bray 2 did not consistently relate well to crop response. A new P soil-test calibration for sugarcane is proposed based on Mehlich 3 soil extraction, with a maximum rate of 36 kg P ha^?1 with ≤ 10 g P m^?3 in preplant soil samples and no P recommended with >30 g P m^?3.