Chemistry of soil potassium in Atlantic coastal plain soils: A review

Abstract

Literature dealing with general properties of soil K and with K relationships in Atlantic Coastal Plain Soils was discussed. Potassium, among major and secondary nutrient elements, is the most abundant in soils. It, among mineral cations required by plants, is largest in non‐hydrated size. Potassium has a polarizability equal to .88 ų and a low hydration energy of 34 kcal g^?1 ion^?1. The major K forms in soils are water soluble, exchangeable, nonexchangeable, and mineral. Various dynamic interrelationships exist between these forms with the reaction kinetics between the various phases determining the fate of applied K.

Many Atlantic Coastal Plain soils contain high levels of total K. Most of the total K in these soils is contained in mineral forms such as micas and K‐feldspars. These K forms are slowly released to solution and exchangeable forms that are available to plants. Many researchers have noted a lack of crop response to K fertilization on Atlantic Coastal Plain soils. This lack of response has been ascribed to the high indigenous levels of mineral and non‐exchangeable K in the soils which would become available to crops. Some researchers have also attributed the lack of response to K accumulations in subsoil from leaching of applied K. If the physical and chemical conditions were favorable in the subsoil horizons, e. g., no pan formation and no severe Al toxicity, plant roots could absorb K from the subsoil horizons.     

Quantity‐intensity parameters of potassium in relation to uptake by guinea‐corn in representative soils of the ecological zones of Nigeria

Abstract

Quantity‐intensity (Q‐I) relation studies were often used to supplement information obtained from conventional soil tests for the estimation of potassium (K) needs of crops. With a view to ascertaining the reliability of the Q‐I relation parameters for comprehensive characterization of K dynamics in typical Nigerian soils, K values derived from Q‐I isotherms were related to neutral normal ammonium acetate (1 N NH₄OAc, pH 7.0) (exchangeable) K, other soil K forms [non‐exchangeable (K_ne), exchange (K_e), mineral K (K _m ), and solution K (K_s)] and the K uptake by Guinea‐corn (Sorghum bicolor, var. LS 187) subjected to weekly cuts in Neubauer cultivation vessels. Most of the soil K (about 98%) was in the form of soil minerals while less than 1% was plant available whereas about 1% was trapped within the interlattice layers of the clay minerals (as fixed K or K_ne). Mineral K (K_m) content was closely related to total K (K_t), but not to the other forms, K_ne, K_e, and K_s. A close relationship was noted between the two components of labile K (K_e and K_s). Except for % K saturation, the relationships between the K measurements with plant response were poor. The results of these investigations clearly demonstrate that the Q‐I relation could not adequately characterize the K dynamics of these tropical soils.     

Characterization of zinc in contaminated soils: complementary insights from isotopic exchange,batch extractions and XAFS spectroscopy

Isotopic exchange (IE) of trace metals is an established method for characterizing metal reactivity in soils, but it is still unclear which metal species are isotopically exchangeable. In this study, we used IE to quantify ‘labile’ zinc (Zn) in 51 contaminated soils that were previously studied by Zn K‐edge X‐ray absorption fine structure (XAFS) spectroscopy and sequential extraction (SE). All soils had been contaminated by runoff water from 17‐ to 74‐year‐old galvanized power‐line towers. They covered a wide range in pH (4.0–7.7), organic carbon (0.9–10.2%), clay (3.8–45.1%) and Zn concentrations (251–30 090 mg kg^?1). Isotopic exchange was also performed on selected Zn minerals used as references for linear combination fitting of XAFS spectra. The isotopically exchangeable fraction (%E) of Zn generally decreased with increasing pH, but small %E values were also observed for acidic soils with a large fraction of Zn in hydroxy‐interlayered minerals (Zn‐HIM). The fraction of Zn identified by XAFS spectroscopy as (tetrahedrally and octahedrally coordinated) ‘sorbed Zn’ agreed reasonably well with the isotopically exchangeable fraction but was in many cases larger than the %E, indicating that some ‘sorbed Zn’ may be isotopically non‐exchangeable, such as Zn sorbed in micropores of Fe oxyhydroxides. Zinc identified by XAFS spectroscopy as Zn precipitates (Zn phyllosilicates, Zn‐layered double hydroxide (Zn‐LDH) or hydrozincite) or as Zn‐HIM was largely isotopically non‐exchangeable (‘non‐labile’). Comparison between IE and extraction results suggested that the isotopically exchangeable Zn was mainly extracted in the first two fractions of the SE. However, non‐labile Zn was also extracted in these first two fractions for some soils, including a hydrozincite‐containing soil. Despite the presence of Zn‐LDH and/or Zn phyllosilicates in almost all soils, the Zn concentrations in solution and labile Zn increased with increasing soil total Zn at a given pH, which contradicts the concept of precipitation control by a single phase. Solution Zn was well predicted from the labile Zn following a sorption model.     

Determination of labile Cu in soils and isotopic exchangeability of colloidal Cu complexes

Measurement of labile (isotopically exchangeable) pools of metals (E values) in soil is required to assess the size of metal pools potentially available to soil organisms, from both a micronutrient deficiency and metal toxicity viewpoint. In this paper, E values of soil Cu were measured by an isotope dilution technique using different solution extracts – water with and without resin purification, water coupled with Donnan dialysis (free ion determination) and 0.01 m CaCl₂. Using these techniques, the isotopic exchangeability of Cu species in water extracts was investigated. The results showed that the specific activity of ⁶⁴Cu in the water‐soluble fraction was less than in the free metal ion fraction or in the fraction that adsorbed to resin. The isotopically non‐exchangeable Cu in water extracts ranged between 4% and 40% of water‐soluble Cu (16% on average), and appeared to be associated with dispersed colloids. The existence of isotopically non‐exchangeable Cu in water extracts led to overestimation (17.7% on average) of isotopically exchangeable Cu in soils when based on the specific activity in water extracts. The method of isotope dilution coupled with resin extraction is recommended for the determination of isotopically exchangeable Cu in soils when water extracts are used.     

Potassium fixation in suspensions of soils of Galicia (N.W. Spain)

Abstract

Potassium (K) fixation in soils treated with K‐rich fertilizer is important in limiting leaching of this ion, and thus the risk of high salinity in waters. We studied this capacity for aqueous suspensions of a group of soils of Galicia (N.W. Spain) and found that fixation increased with K dosage, increased slightly with contact time, and decreased with increasing temperature (between 3 and 40°C). Potassium fixation was barely influenced by the mineralogy of the clay fraction but was greater in soils with greater fine particle content. Modified Freundlich equation successfully modelled the effects of K addition, temperature, and contact time on fixation. The influence of temperature was greater in illitic soils than in mixed soils. The results indicate that Galician soils have little capacity for K fixation.     

Distribution of potassium fractions in sweet potato (Ipomoea batatas) garden soils in the Central Highlands of Papua New Guinea and management implications

Previous studies indicated that potassium (K) deficiency is an important soil‐related factor for yield decline of the sweet potato gardens in the Central Highlands of Papua New Guinea, where sweet potato is an important staple food crop. An effort was made to characterize various fractions of K in the diverse soils of this region under sweet potato, to ascertain the probable reasons behind the observed K deficiency and its relationship to decreasing yield trends. Soils from two depths (0–10 cm) and (10–20 cm) in two types of gardens (old and new gardens) were assessed for different fractions of soil potassium in volcanic and non‐volcanic soil groups. Volcanic soils (Hydrandepts and Andaquepts) were significantly lower (P < 0.05) in exchangeable K than the non‐volcanic soils (Dystropepts, Tropoqualfs and Eutropepts). Mean exchangeable K content of the non‐volcanic soils was 95.5 mg/kg, whereas that of volcanic soils was 72.4 mg/kg. Similarly, new gardens had an average exchangeable K content of 94.1 mg/kg, which was significantly greater than 71.6 mg/kg soil of older gardens. Non‐exchangeable K content differed significantly (P < 0.001) between the soil types; mean K content was 85.9 mg/kg for the volcanic soils, whereas in non‐volcanic soils, it was 184.9 mg/kg. Garden types also differed significantly (P < 0.05) with respect to non‐exchangeable K content; new gardens registering higher average values (by almost 20%) than the older gardens. Multiple regression analysis showed that variability in the tuber yield was as a result of variability of water soluble and exchangeable K (up to 22%), non‐exchangeable K (2%), mineral K (4%) and leaf K concentrations (10%). Older gardens, which are in volcanic soil groupings, are more susceptible to the K depletion problem because of continuous sweet potato cultivation, possibly owing to their lower K reserves. Such gardens should be managed either with sufficient fallow periods for regeneration of soil fertility or with suitable application of mineral K fertilizers to enhance productivity.     

Fractionation of soil cadmium from some new zealand soils

Abstract

The concentrations and forms of soil cadmium (Cd) in 12 different New Zealand topsoils were investigated using a sequential fractionation procedure. Total soil Cd concentrations were low and ranged between 0.03 μg g^‐1 to 1.34 μg g^‐1 and were highly correlated with total soil phosphorus (r²=0.85, P<0.01). Results indicated that there was a wide range in the concentrations of Cd associated with individual soil fractions and large variations between soils. On average for all soils, the smallest proportion of Cd was in exchangeable forms, i.e., 3%, with 12% in the crystalline oxide fraction, 13% in the amorphous oxide fraction and the greatest proportion of Cd associated with the organic 34% and residual 38% fractions. There was evidence to show that a soil extractant which is commonly used to predict plant uptake of Cd from soils, i.e., 0.04 M ethylene diamine terra acetic acid (EDTA), extracts Cd from both exchangeable and organic forms of soil Cd.     

Potassium status of some selected soils under different land‐use systems in the subhumid zone of Nigeria

Abstract

Twenty surface soils (0 to 15 cm), selected to represent a wide range of available potassium (K) status and three different land‐use systems (fodder bank, continuously fertilized cropped land and fallow land) across the subhumid zone of Nigeria, were used for the investigation. Laboratory and greenhouse studies were carried out to assess their K status. Available, non‐exchangeable, and total K were determined. The supplying power of the soils was assessed by exhaustive cropping in the greenhouse using Stylosanthes hamata cv. Verano as the indicator plant. While 75% of fodder banks sampled had available K less than 0.20 cmol/kg, only 50% and 13% of continuously fertilized cropped and fallow lands, respectively, had available K less than 0.20 cmol/kg. Potassium weathering coefficient was highest at the lowest exchangeable K and highest [calcium (Ca) + magnesium (Mg)]/K ratio. Total K ranged from 2.30 to 47.06 cmol/kg, with available K forming 1.47% of the total K. The amount of non‐exchangeable K released and taken up by stylo plant accounted for 23.3 to 83.6% of the total K uptake.     

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.     

Evaluation of Nutrient Release in Salt‐Saturated Soils

Abstract

The effects of irrigating with saline water on native soil fertility and nutrient relationships are not well understood. In a laboratory experiment, we determined the extent of indigenous nutrient [calcium (Ca), magnesium (Mg), potassium (K), manganese (Mn), and zinc (Zn)] release in salt-saturated soils. Soils were saturated with 0, 75, and 150 mmolc L^?1 sodium chloride (NaCl) solution and incubated for 1, 5, 10, and 15 days. The saturation extracts were analyzed for pH, ECe, and water‐soluble Ca, Mg, K, Mn, and Zn, and the remainder soil samples were analyzed for exchangeable forms of these elements. In a subexperiment, three soil types (masa, red‐yellow, and andosol) were saturated individually either with 100 mmolc L^?1 of NaCl, sodium nitrate (NaNO₃), or sodium sulfate (Na₂SO₄) salt. These salts were also compared for nutrient release. Soils treated with NaCl released higher amounts of water‐soluble than exchangeable nutrients. Except for Zn, the average concentrations of these nutrients in the soil solution increased significantly with time of incubation, but concentrations of the exchangeable forms varied inversely with time of incubation. The masa soil exhibited the highest concentrations of Ca and Mg, whereas K was highest in andosol. The extract from soils treated with NaCl contained greater amounts of soluble cations, whereas soils treated with Na₂SO₄ produced the lowest concentration of these elements irrespective of the type of soil used.     

Fractionation of zinc in some New Zealand soils

Abstract

The amounts and forms of zinc in twenty surface soils from Canterbury and Southland, New Zealand were determined using a sequential fractionation scheme. Total soil zinc concentrations ranged from 38.1 mg#lbkg^‐1 to 113.8 mg#lbkg^‐1. Although the proportions of zinc found in individual fractions varied between soils, on average approximately 3% occurred as exchangeable zinc, 5% as organic‐bound zinc, 9%, 18%, 24% was associated with manganese, amorphous iron and crystalline iron oxides, respectively, and 40% was in the residual fraction. In a group of soils formed in greywacke alluvium or loess, exchangeable zinc was inversely related to soil pH. Within the same group of soils, those of similar age with greater concentrations of total and organic‐bound zinc were present in imperfectly‐ and poorly‐drained soils compared with well‐drained soils. Zinc extracted from the soils with a range of reagents used to assess ‘plant available’ zinc was correlated strongly with the concentrations of zinc present in the exchangeable and organic‐bound zinc fractions.     

Differential potassium buffer behavior of individual soils related to potassium corrective treatments

Abstract

Although the basic chemistry and behavior of potassium in the soil is well understood, little of this knowledge is used in soil testing and practical soil fertility mangement. In this study the K buffer behavior of three individual soils (Hagerstown silt loam (Typic Hapludalf), Gatesburg sand (Entic Haplorthod) and Gilpin channery silt loam (Typic Hapludult)) was investigated. The buffer relationships determined indicated very different K behavior for these soils even though exchangeable K soil tests indicated similar K levels. It was also determined that for these soils the buffer relationship was apparently independent of previous K management, indicating that the K buffer behavior could be included as part of soil characterization data.

The role of nonexchangeable K in determining K buffer behavior was also investigated. It was found that the levels of solution K where the release of nonexchangeable K becomes measurable (0.27 ‐ 0.83 × 10^‐4 M) are similar to solution K levels reportedly required for crop growth (0.02 ‐ 0.95 × 10^‐4 M). It was also found that these soils were capable of maintaining a relatively high level of exchangeable K even after extraction of significant amounts of nonexchangeable K with sodium tetraphenyl boron.

It was concluded that K buffering behavior of individual soils could and should be included in K management decisions involving corrective soil treatments and/or crop removal estimation. Otherwise, based on current soil tests, soils with very different K buffer behavior will be treated similarly.     

Aluminum and iron estimated by Mehlich‐3 extractant in mine soils in Galicia,northwest Spain

Abstract

The efficiency of Mehlich‐3 reagent as an extractant for aluminum (Al) and iron (Fe) was studied in Galician coal mine soils, in the process of reclamation. Mehlich‐3 Al and Fe values were compared to those from other Al and Fe tests and with phosphorus (P) sorption. The soils are very heterogeneous, consisting mainly of carbonaceous and non‐carbonaceous clays and shales, which are often rich in pyrite. Some of them have been amended with topsoil or fly ash. One hundred forty samples, from 0 to 15 or 15 to 30 cm, were analyzed. The pH values ranged from 2.7 to 8.4; oxalate and pyrophosphate Al from 0 to 1.17%, and 0.02 to 0.58%, respectively; and oxalate and pyrophosphate Fe from 0.02 to 2.25% and 0 to 1.28%, respectively; PSI (P sorption index) values varied between 0 and 55.1. The Mehlich‐3 Al values ranged from 24 to 2600 mg kg^‐1. A close relationship was observed between Mehlich‐3 and oxalate Al values (r=0.77), although the regression line tended to be curvilinear. Mehlich‐3 Al was better correlated than oxalate Al to pyrophosphate Al (r=0.66 vs. r=0.59) and also to pH‐NaF (r=0.89 vs. r=0.74). The Mehlich‐3 Al is almost as good as oxalate Al in estimating non‐crystalline Al, the correlation coefficients between log PSI and log (Mehlich‐3 Al) or log (oxalate Al) being 0.51 and 0.57, respectively. The Mehlich‐3 Fe correlated to available (r=0.63), exchangeable (r=0.65) and soluble Fe (r=0.66), but not to non‐crystalline Fe.     

Potassium potential and potential buffering capacity of torripsamments in the United Arab emirates

Abstract

Eighteen surface soil samples from five locations were collected to represent the Torripsamments in the United Arab Emirates. The quantity‐intensity (Q/I) relationships were determined for the soils. They were linear over the range of activity ratios commonly encountered in the studied soils. The soil solution potassium (K) activity relative to the calcium (Ca) + magnesium (Mg) at equilibrium (ARKe) ranged between 0.0034 and 0.0396 (M/L)^0.5. The readily exchangeable K (Kre) values ranged between 0.009 and 0.069 cmolc/kg which represented an average of 23% of the exchangeable K. A negative relation was found between K‐feldspars and K_re values (r = ‐ 0.573**), indicating that K‐feldspars contributed little to available K in the studied soils. The soils showed low capacity to maintain the potential of K against depletion, as they showed very low potential buffering capacity #OPPBCK#CP [1.21–5.68 (cmoLc/kg)/(M/L)^0.5].     

Exchangeable K levels for maximum crop yields on soils of different cation exchange capacities

Abstract

Wide differences in levels of exchangeable K considered adequate for maximum yields in different States are probably a consequence of the acceptance of either a single 200 pp2m rate for 95–987. sufficiency suggested by Bray, or a variable level based on a percentage of the soil cation exchange capacity (CEC) proposed by Bear. It now appears that sufficiency levels should vary with soil CEC, but not merely as a simple percentage of it. Moreover, the relatiorshlp in practice is complicated by such factors as leaching of K from coarse textured soils, and fixation of added K in, and release of native K from, non‐exchangeable forms in soils high in micaceous clay content. Since these influences occur widely in Ohio soils, the need for new field studies was recognized and implemented. Laboratory and growth chamber studies relating K sufficiency to energies of exchange were examined. Also, a new procedure used by the Ohio Soil Testing Laboratory for providing K sufficiency baaed on soil CEC and crop yield and composition is described.     

Potassium uptake by soybean as affected by exchangeable potassium in soil

Abstract

Soybean (Glycine max (L.) Merrill) has been shown to have a great capacity to take K from soil, suggesting that it might absorb K from non‐exchangeable forms. In this paper, the effect of level of K fertilization on soil exchangeable K content and K uptake by soybean are discussed. The experiment was conducted on a Typic Haplortox (sandy loam), fertilized with 0, 40, 80, 160 and 240 kg K₂O/ha as KC1 or K₂SO₄. During five years before the experiment, half of the plots received those K rates annually and the other half only in the first three years, providing an opportunity to study the residual effect of applied K. Plant samples were taken at pod filling and at harvest. Soil cores were collected in 20 cm increments down to 80 cm deep at plant emergence, pod filling and after harvest. There was a residual effect of K, and 240 kg K₂O/ha applied in a 3‐year term led to the same yield and K uptake as 80 kg ICO/ha applied annually for 3 years. Fertilized plants absorbed 160% more K than unfertilized ones, but soil exchangeable K accounted for less than 50% of plant uptake; therefore the exchangeable pool must have been replaced in time for soybean uptake. On the other hand, the K recycled from the plant to the soil was not found in the exchangeable form. There was evidence of K leaching deeper than 80 cm, and in addition, the K recycled from the plants may have turned into non‐exchangeable forms in the soil.     

Potassium availability in soils from different parent materials in the subhumid zone of Nigeria

Abstract

Potassium (K) availability was assessed in 21 soil samples from four different parent materials (alluvium, iron pan materials, Nupe sandstones, and colluvial materials) across the subhumid zone of Nigeria. It was found that the Nupe sandstone soils gave the lowest proportion of the various forms of K with respect to total K in the topsoil. While water‐soluble K was the lowest in the soils of all the parent materials, one normal hydrochloric acid (1 N HCl)‐extractable K was the highest in the soils of all the parent materials. The one normal ammonium acetate (1 N NH₄OAc)‐extractable K (exchangeable K) was correlated (P<0.05) with exchangeable calcium (Ca) and magnesium (Mg) in the alluvial, iron pan material and colluvial material soils and with clay in the soils of all the parent materials. The K fixed in the 42 days of incubation was highly correlated (P<0.01) with the K added in the colluvial material soils.     

Phosphorus retention in some soils of the Argentinean Mesopotamia

Abstract

Phosphorus (P) sorption isotherms were derived for 13 soils of the Argentinean Mesopotamia with a wide range of physicochemical properties. Shaking time varied from 1 to 24 hours in order to estimate the phosphate buffering capacity (PBC), maximum P sorption capacity (MPSC), and P sorption energy (PSE). In addition, six rates of P, allowed to react with soil at field capacity for 63 days and labile P, non‐labile P, and P in solution, were assessed after that time. The retention capacity of these soils ranged from medium to very low and P sorption was correlated not only with the content of amorphous aluminum (Al) and iron (Fe), but with the clay percentage of soils. Organic carbon was a variable not related to P retention. After two months, soils with more P fixation showed about 70% of the added P became non‐labile with insignificant amounts in solution. In those showing low retention, P was distributed in the following proportion: 50 to 60% non‐labile, around 40% labile, and less than 10% in solution, whereas for sandy soils, of very low fixation, 10 to 20% remained in solution and less than 40% became non‐labile. The increase in the total P due to fertilization resulted in a relative increase in the more available forms for plants. At the same time, a proportional decrease of non‐labile P was observed.     

Exchangeability of phosphate extracted by four chemical methods

Isotopically exchangeable phosphate (P) is a major source of P for plants. In practice, however, plant‐available P is assessed by chemical extractions solubilizing a mixture of P forms the availability of which is ill defined. We undertook an isotopic approach to assess the exchangeability of P extracted by (1) CO₂‐saturated water (P‐CO₂), (2) ammonium acetate EDTA (P‐AAEDTA), and (3) sodium bicarbonate (P‐NaHCO₃) compared to the exchangeability of P extracted by water. Five topsoils with similar P‐fertilization histories but different soil properties were studied. Phosphorus was extracted from soils labeled with carrier‐free ³³P after 1 week of incubation, and the specific activity (SA = ³³P / ³¹P) of the extracts was compared with the SA of P extracted by water to calculate the amount of P isotopically exchangeable that had been solubilized during the extraction. P‐CO₂ extracted between 20 and 100 times less P than P‐AAEDTA and P‐NaHCO₃. The SA of P‐CO₂ was not different from the SA of water‐extractable P, showing that P‐CO₂ solubilized similar forms of P as water and that these forms can be considered as available. The SA of P extracted by the two other methods ranged between 25% and 63% for P‐AAEDTA and 66% and 92% for P‐NaHCO₃ of the SA of water‐extractable P. The fraction of exchangeable P extracted by AAEDTA decreased linearly with increasing soil pH, suggesting that this method dissolves slowly or non‐exchangeable P from calcium phosphates.     

Potassium isotherm partitioning based on modified quantity‐intensity relation and potassium buffering characterization of soils of North India

Background : Potassium (K) availability in soil and plant uptake is restrained by the dynamic interactions among the different pools of K. Aims : To understand these interactions, a study was undertaken to assess the quantity–intensity (Q/I) and buffering characteristics of rainfed maize (Zea mays L.) growing soils. Ten contrasting soils were evaluated for K partitioning changes in exchangeable K (ΔEK) and non‐exchangeable K (ΔNEK) pools in the soil‐solution phase and buffering characteristics using a modified version of Q/I approach. Results : The partitioned Q/I isotherms showed strong adsorption with the increase in K concentration ratio (CR^K) and the changes due to ΔEK were higher than changes due to ΔNEK. Total buffering capacity (PBC^K) significantly correlated (r = 0.92, p <0.01) with clay content with a major share contributed by buffering capacity owing to non‐exchangeable K ( ${\mathrm{PBC}}_{\Delta \mathrm{NEK}}^K$) rather than exchangeable K ( ${\mathrm{PBC}}_{\Delta \mathrm{EK}}^K$). The fixation capacity (β) factor, the magnitude of added K converted into a non‐exchangeable pool, ranged from 41 to 63%, whereas release (α) factor, the magnitude of added K converted to the exchangeable pool, ranged from 19 to 36%. Both threshold solution K (CK_r) and threshold exchangeable K (EK_r) values were found to be high in Satran clay loam (S2) and lower in Doon silty clay loam (S3) soils. The equilibrium exchangeable K (EK_o) was found close to minimum exchangeable K (E_min) in Doon silty clay loam (S3) and Babaweyl sandy clay loam (S1) soils and overall E_min constituted about 8.94 to 0.57% of the EK_o. Conclusion : It may be concluded that K Q/I isotherm partitioning provides a valuable insight to assess the dynamic relations. The ratio of α/β (K recharge index) could be used to evaluate the K enrichment capacity of soil to K additions while EK_r and E_min can be potentially useful in the elucidation of exchangeable K as K fertility index especially in soils with poor K fertilizer management.