Phosphorus (P) is a vital soil macronutrient required by plants for optimum growth and development. However, its availability is limited because of fixation. The phosphorus fixation reaction is pH dependent. In acid soils, the predominance of aluminium (Al) and iron (Fe) oxides in both crystalline and amorphous forms reduces the solubility of soil inorganic P through fixation on positively charged surfaces and formation of insoluble Al and Fe precipitates. In alkaline soils, P readily reacts with calcium (Ca) to form sparingly soluble calcium phosphates. As a result, a large proportion of applied P may become chemically bound, whereas only a small fraction of soil P remains in the soil solution and available for plant uptake. To date, there is little information available on the use of charcoal with a highly negative charge and wood ash with high alkalinity to minimise P fixation in acid soils. Thus, this study examined the potential of the combined use of charcoal and wood ash to unlock P fixation in acid soils. Numerous studies have been conducted to identify effective approaches to improve P availability through the use of different types of soil amendments, regardless of whether P is organically or inorganically present. For example, to mitigate P fixation in acid soils, amendments such as compost and zeolite are used to reduce P sorption sites. These amendments have also been used to increase P uptake and crop productivity in P deficient acid soils by reducing soil acidity and the toxicity of Al and Fe. It is believed that long-term application of charcoal and sago bark ash can positively change the physical and chemical properties of soils. These improvements do not only reduce P fixation in acid soils, but they also promote an effective utilisation of nutrients through timely release of nutrients for maximum crop production.

The high costs of nitrogen fertilizers have necessitated best-developed practices to optimize nitrogen fertilizers use whilst minimizing nitrate losses. Ammonium adsorption inhibits loss of nitrogen in the form of nitrate thereby increasing nitrogen availability for crops. Due to the negatively charged properties of nitrate, it moves freely in the soil solution and not adsorbed onto soil particle surfaces. In this study, clinoptilolite zeolite was used in soil leachingand ammonium adsorption and desorption studies to determine: (i) soil total nitrogen availability, exchangeable ammonium, and available nitrate, and (ii) the capacity of clinoptilolite zeolite to adsorb and desorb ammonium from different rates of urea. Different rates of urea amended with clinoptilolite zeolite significantly reduced ammonium and nitrate release from urea compared with urea alone. Clinoptilolite zeolite enhanced retention of soil total nitrogen, exchangeable ammonium, and available nitrate due to the high cation exchange capacity of the mineral to adsorb ammonium, thus, improving nitrogen availability through temporary retention on the exchange sites of the clinoptilolite zeolite. The availability of nitrogen can be enhanced if urea is amended with clinoptilolite zeolite.

Improper use of urea may cause environmental pollution through NH3 volatilization and NO3 − leaching from urea. Clinoptilolite zeolite and compost could be used to control N loss from urea by controlling NH4 + and NO3 − release from urea. Soil incubation and leaching experiments were conducted to determine the effects of clinoptilolite zeolite and compost on controlling NH4 + and NO3 − losses from urea. Bekenu Series soil (Typic Paleudults) was incubated for 30, 60, and 90 days. A soil leaching experiment was conducted for 30 days. Urea amended with clinoptilolite zeolite and compost significantly reduced NH4 + and NO3 − release from urea (soil incubation study) compared with urea alone, thus reducing leaching of these ions. Ammonium and NO3 − leaching losses during the 30 days of the leaching experiment were highest in urea alone compared with urea with clinoptilolite zeolite and compost treatments. At 30 days of the leaching experiment, NH4 + retention in soil with urea amended with clinoptilolite zeolite and compost was better than that with urea alone. These observations were because of the high pH, CEC, and other chemical properties of clinoptilolite zeolite and compost. Urea can be amended with clinoptilolite zeolite and compost to improve NH4 + and NO3 − release from urea.

The availability of paddy husk from rice processing plants remains high owing to increase in the worldwide rice consumption. Increasing demand for chicken products leads to poultry wastes production. Co-composting of the aforementioned wastes could solve the indiscriminate disposal of these wastes. Thus, co-composting of paddy husk and chicken slurry with clinoptilolite zeolite and urea as additive was carried out. Clinoptilolite zeolite was used to enhance ammonium and nitrate retention in the compost. Temperature of the compost was monitored three times daily for 55 days. Cation exchange capacity, organic matter, ash, humic acids, pH, total C, N, C/N ratio; total P, exchangeable Ca, Mg, K, NH4+, NO3-, and heavy metals contents were determined using standard procedures. pH, total N, humic acids, ash, NH4+, NO3-, P, Ca, Mg, and K contents increased but the salinity, heavy metals contents, and microbial population were low after the co-composting process. Zea mays L. (test crop) seed germination rate in distilled water and the compost were not significantly different. Growth of Spinach oleracea (test crop) on a peat-based growing medium and the compost was also not significantly different. These findings were possible because the clinoptilolite zeolite used in co-composting reduced accumulation of heavy metals that may have damage effects on the test crops. Mature compost with good agronomic properties can be produced by co-composting chicken slurry and paddy husk using clinoptilolite zeolite and urea as additives.

Adsorption and desorption of nitrogen (N), phosphorus (P), and potassium (K) soils are controlled by pH, pH buffering capacity, organic matter, and cation exchange capacity (CEC). These factors optimized to improve timely availability of N, P, and K crop use using organic amendments such as chicken litter biochar (CLB). The objective of this study was to determine the effects of CLB on N, P, K sorption and pH buffering capacity of an acid soil. Different rates of CLB were mixed with an acid soil for N, P, and K sorption and pH buffering capacity determination. The CLB increased soil pH and pH buffering capacity, but unlike P and K adsorption, the different rates of CLB significantly increased N adsorption, suggesting that this soil amendment has high affinity for N than P and K. Also, because CLB reduced N, P, and K desorption, it suggests that N in particular will be slowly released with time. The reduced N desorption but higher N adsorption further indicates that N can be temporary fixed by CLB. This work has revealed CLB is more effective controlling soil N availability for timely crop use to avoid losses.