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Excess of exchangeable sodium (Na) in salt-affected soils causes ion toxicity and decrease in nutrient uptake by plants, particularly potassium (K). A number of studies have been conducted to investigate the effect of K-fertilization on plant growth under sodic and saline-sodic conditions but the results are much diverse to process for concrete recommendations. To explore the possible reasons, it was hypothesized that Na applied as NaCl to produce salinity/sodicity in the soil may release non-exchangeable K, minimizing the effect of K-fertilization. Incubation studies were conducted for 2, 4 and 6 days in the light (sandy loam) and heavy (clay loam) textured soils producing two saline/sodic levels, i.e. 20 and 30 sodium adsorption ratio (SAR) along with control (SAR 3). Potassium fertilizer applied was calculated according to 40 (general recommendations based on soil-nutrient status), 80 and 160 kg K ha−1. Interestingly, it was observed that addition of NaCl possibly released non-exchangeable K from the soil minerals and increased the K concentration in soil solution. Total K release was more in heavy textured soil but initial release was more in light textured soil. This release may eliminate the effect of K-fertilization applied under salt stress induced by NaCl. Therefore, it is suggested that while studying Na–K interaction in salt-affected soils, NaCl should be avoided to produce salinity, and naturally occurring saline-sodic soils may be used. Soil Na–K interaction studies including ameliorating effect of K under sodic or saline-sodic conditions should be conducted carefully considering the above-stated argument. [ABSTRACT FROM PUBLISHER]

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. [ABSTRACT FROM AUTHOR]