Lowering ammonia volatilization losses from urea application by activation of nitrification process

The aim of this work was to lower ammonia volatilization losses by increasing the rate of nitrification. This was achieved by eliminating the gap in timing between urea hydrolysis and ammonium nitrification. Soils were pretreated with a small amount of ammonium salt which led to the activation of the nitrification process. When nitrification passed its lag period, urea was applied to the soils. Ammonium produced by urea hydrolysis was quickly oxidized into nitrate and did not accumulate in the soil. This resulted in decreased ammonium concentrations in soil, and consequently, in decreased ammonia volatilization losses.This report is part of a doctoral thesis by the first author.     

Effects of initial soil calcium content on ammonia losses from surface-applied urea and calcium-urea

Ammonia loss from surface-applied urea occurs because urea hydrolysis increases the pH of the placement site microenvironment. Addition of Ca-salts with urea will control or reduce the microsite pH, thus reducing NH₃ losses. The degree of Ca-saturation of the cation exchange sites may influence the ratio of calcium:urea required to control ammonia loss. A laboratory study was conducted to determine if adsorbed Ca or CaCO₃ additions (acid soils only) had a measureable impact on Ca control of NH₃ loss from surface applied urea at various Ca:urea ratios.With urea alone applied to the soil surface varying the adsorbed Ca content of the treatment soil did not influence NH₃ loss. The addition of CaCl₂ with urea on the same pretreated soils generally resulted in NH₃ losses reflecting the initial pH of the soil. The Ca-saturated acid soils and those acid soils receiving CaCO₃ had higher NH₃ losses than untreated soils in the presence of urea with soluble CaCl₂. It was noted that increasing the calcium:urea ratios progressively depressed the NH₃ loss from all soils. Increasing the percent Na-saturation of the calcareous Harkey soil to 25 and 50% (ESP) reduced Ca control of NH₃ loss due to Ca being exchanged for Na on the cation exchange sites.Inclusion of CaCl₂ with the urea mixture on the surface of the pretreated acid soils resulted in stepwise differences in NH₃ loss concuring with the increases in pretreatment soil pH values (differing exchangeable Ca content). Other parameters that influence the amount of NH₃ loss, such as acidic buffer capacity and CEC, appeared more important than anticipated for control of NH₃ loss with the calcium:urea mixture. On Ca enriched soils the calcium:urea mixture was only slightly less effective in its ability to control NH₃ losses than on untreated soils.Contribution from the Texas Agric. Exp. Sta., Texas A&M University System, College Station, TX 77843, USA     

A comparative study of urea hydrolysis rate and ammonia volatilization from urea and urea calcium nitrate

A comparing of urea hydrolysis and NH₃ volatilization from urea supergranules and urea calcium nitrate (UCN, a new fertilizer produced by Norsk Hydro A/S, Norway) was made on two different flooded soil types, a high-CEC clay loam (Ås) and an intermediate-CEC clay loam (Kinn).Nitrogen loss by ammonia volatilization was reduced from 17% by surface application of urea supergranules (USG) on flooded Ås soil to 3% and 6% by UCN briquettes at either the same urea or nitrogen concentration as USG. A significant reduction was even found with the surface application of prilled UCN, 12% and 18% N-loss for prilled UCN and urea, respectively. The floodwater pH and NH ₄ ⁺ content was lower with UCN than urea, which reduced the potential for ammonia volatilization.NH₃-loss (5%) was significantly less when USG was surface applied on Kinn soil, while NH₃-loss from UCN briquettes was independent of soil type. The reduction in NH₃-loss from USG on Kinn soil was due to a decrease in the pH and NH ₄ ⁺ content of the floodwater caused by a reduced rate of urea hydrolysis.The rate of urea hydrolysis was lower with UCN than USG in both soils, but the difference between UCN and USG was greater in the Ås soil than in the Kinn soil. Three days after deep placement (10 cm), 18% of UCN urea and 52% of USG urea were hydrolyzed in Ås soil, while only 12% UCN and 17% USG were hydrolyzed in the Kinn soil.The surface application of USG on flooded soil reduced the rate of urea hydrolysis as compared to deep placement. 30% and 17% of USG urea was hydrolyzed after four days on Ås and Kinn soil, respectively. During the first few days the rate of hydrolysis of UCN was more affected by the soil type than the application method. Four days after surface application 32% and 13% UCN urea was hydrolyzed on Ås and Kinn soil, respectively. The rate of urea hydrolysis exhibited a zero-order reaction when USG and UCN-briquettes were point placed in flooded soils.     

A comparison of methods of estimating ammonia volatilization in the field

Accurate estimation of the potential for NH₃ volatilization from urea-based fertilizers is an important step in attaining optimum N-use efficiency from these fertilizers. Published estimates of NH₃ volatilization losses from urea vary widely. Much of this variability may be due to the method of estimation and the degree of influence of the method on NH₃ loss. This study compared two field methods of estimating NH₃ volatilization in the field; a microplot-forced draft method, and a micrometeorogical method. Loss of NH₃ was estimated in three experiments following urea solution application to bare soil, and in two experiments following urea-ammonium nitrate solution application to wheat stubble residue. Both methods were found to be sensitive to soil and climatic variables influencing NH₃ volatilization. Cumulative N loss from the bare soil experiments ranged from 7 to 8 kg N ha^–1 for the microplot method and from 5 to 20 kg N ha^–1 for the micrometeorological method. Cumulative loss from wheat stubble residue ranged from 2 to 2.2 kg N ha^–1 for the microplot method and from 15 to 33 kg N ha^–1 for the micrometerological method. Loss of NH₃ was especially influenced by soil or residue water content and the influence of water content on the rate of urea hydrolysis. Maximum rates of loss were generally observed near midday, when water content at the soil surface was just beginning to decline and the surface temperature was rapidly rising. The microplot method was found to have a greater potential for affecting the environment and thus influencing NH₃ loss measurements than the micrometeorological method. Windspeed and mixing at the soil surface was influenced by the presence of the microplot cylinder and lid, especially in the wheat residue experiments. It is likely that the micrometeorological method, with its minimal influence on the field environment, more accurately reflects actual levels of ammonia loss. The primary advantage of the microplotforced draft method is its ability to easily compare relative NH₃ losses from different treatments.Contribution No. 87-300-J from the Kansas Agricultural Experiment Station. Part of a dissertation submitted by the senior author in partial fulfillment of the requirements for the Ph. D. Degree at Kansas State University. The research was supported in part by grants from Farmland Industries, Inc., and USDA-ARS.     

Effect of magnesium sulphate addition to urea on nitrogen loss due to ammonia volatilization

Fertilizer was applied as urea alone or as a mixture of urea and magnesium sulphate (MgSO₄·1H₂O) to study the effect on ammonia volatilization under laboratory conditions in relation to soil texture, N:Mg ratio, air flow rate, fertilizer form (solid or liquid) and organic material. When the mixture of urea and magnesium sulphate (UMM) was applied at a ratio of 1:0.21, significantly lower NH₃-N losses than from urea were found in 2 of 6 soils, and 4 soils showed a similar tendency. Increasing the N:Mg ratio to 1:0.5 resulted in significantly lower NH₃-N loss. Lower air flow rates reduced ammonia loss from UMM more than from urea alone. The effectiveness of UMM over urea was not improved in the liquid form. Increase of organic material had no influence on NH₃-N loss from urea alone or UMM.     

Impact on ammonia volatilization losses of mixing KCl of high pH with urea

Ammonia volatilization associated with urea hydrolysis has been shown to be primarily associated with the pH of the soil solution and its buffering ability in the immediate zone of the fertilizer granule. Numerous studies have also shown that these losses can be reduced significantly by the addition of large amounts of KCl with the urea. Because the pH of commercial sources of potash ranges from 6.5 to 9.5, investigations were conducted to determine if the high pH of these K sources had an effect on the ammonia lost from three contrasting soils. Despite large ammonia losses (approximately 50% of N applied) and a significant reduction in loss due to the use of KCl (30%-50% reduction), the experiments showed no effect of potash pH on ammonia loss. It may be concluded that no risk of enhanced ammonia loss can be associated with the use of high-pH potash sources.     

Predicting the effect of soil-water-air dynamics on ammonia volatilization from applied urea with a mechanistic model

To assess the influence of varying soil water and soil air contents on ammonia volatilization from surface applied urea, a mechanistic model is used to simulate the system. The results are discussed in terms of the effects of soil-water-air dynamics on the movement of urea, ammoniacal-nitrogen and soil base, and on the rate of urea hydrolysis, and their influence on ammonia volatilization. Changing the soil moisture between 90% and 125% of field capacity did not have a marked influence on ammonia volatilization. The predicted losses were at their minimum with a moisture content slightly above field capacity, and increased sharply as the soil moisture fell below 90% of the field capacity. Ammonia volatilization losses measured by experiment at differentf values agreed very well with those predicted by the model. The relative contribution of the liquid pathway over the gaseous pathway of movement of NH₃ through soil increased with increase inf, and, at a givenf, decreased with increase in the pH.     

The influence of sward mass,defoliation and watering on ammonia volatilization losses from an Italian ryegrass sward topdressed with urea

Using intact pasture sods with 0.15m² surface area and sealed in volatilization chambers, the influence of the mass of herbage on the ammonia volatilization losses following a surface application of urea was determined. Ammonia volatilization loss increased as sward mass decreased. This effect was still evident in poorly established pastures.Under drying conditions the timing of defoliation and water applications relative to the application of urea was also shown to influence ammonia volatilization patterns and magnitude of loss. Delaying defoliation promotes a reduction in ammonia volatilization losses while delayed watering resulted in increased losses.     

Dynamics of ammonia volatilization from simulated urine patches and aqueous urea applied to pasture. II. Theoretical derivation of a simplified model

Theoretical considerations for the development of a simplified model for predicting volatilization losses of ammonia gas (NH_3(g)) from the urine patches of grazing herbivores in a pasture ecosystem are presented. The volatilization of NH_3(g) is treated as a physico-chemical phenomenon based on the soil solution chemistry of urine patches to develop a general equation to describe the rate of volatilization from a pasture surface. A semi-empirical approach was then used in which published data define typical limits for the parameters appearing in the volatilization equation. This led to the simplification of the general volatilization equation into a more useable and more readily verifiable form.The dominant factor in determining the rate of volatilization of NH_3(g) was shown to be the soil surface pH. To better understand the dynamics of pH changes within urine patches, the more extensive literature dealing with volatilization losses from flooded soils was reviewed. From the apparent similarities between the two systems a procedure was described by which a careful monitoring of soil surface pH as a function of time could be used to solve the simplified equation.To calculate NH_3(g) fluxes this model requires the following as input data: a knowledge of the disposition of the applied-N within the soil profile; the rate of urea hydrolysis in the topsoil; and soil surface pH and temperature measurements throughout the duration of a volatilization event.     

Effect of soil bulk density on hydrolysis of surface-applied urea in unsaturated soils

In situ hydrolysis of broadcast urea occurs in unsaturated soils with different bulk densities. The effect of increasing soil bulk densities on the hydrolysis of urea was studied in open and in covered unsaturated soil columns incubated at 30°C. An increase in bulk density from 0.8 to 1.4 Mg/m³ markedly increased the hydrolysis of surface-applied urea in soils containing water > 6% up to near field capacity. Increased diffusion of urea to sorbed soil urease with an increase in bulk density may have enhanced formation of urease-urea complexes and therefore increased the hydrolysis. As urea diffused farther in more dense soils, the retarding effects of high urea concentration gradients on the hydrolysis probably decreased. In light-textured soils, increases in the bulk density had no apparent effect on the hydrolysis of surface-applied urea when evaporation occurred.     

Effect of amounts and sequence of additions of urea and water on hydrolysis of surface-applied granular urea in unsaturated soils

The hydrolysis of surface-applied granular urea ( 15 mg of urea/particle) in 14 unsaturated soils as influenced by the amounts and the sequence of additions of urea and water and studied using open and covered soil column systems was in the following order: well-mixed surface-applied surface-applied surface-applied urea, granular urea, granular urea, granular urea, water added > water added > water added water added before, after, before, before, no drying no drying no drying drying The retarded hydrolysis' of surface-applied granular urea is attributed to retarded soil urease activity. Under the nondrying and drying conditions, the positive effect of increasing amounts of added water on the hydrolysis was less apparent when water was added 24–48 hours before than when it was added immediately after surface application of granular urea. When an increasing number of urea granules were evenly placed on a finite surface of unsaturated soil, the rate of urea application (quantity factor) increased but the percentage of urea hydrolyzed remained practically unchanged. These results suggest that it is necessary to consider effective urea concentration and effective urease activity for adequate understanding of in situ hydrolysis of broadcast fertilizer urea in unsaturated soil.     

Dynamics of ammonia volatilization from simulated urine patches and aqueous urea applied to pasture. III. Field verification of a simplified model

Published field experimental data [11, 15, 19] were used to compare measured NH_3(g) losses following applications of urine or aqueous urea to pasture soils with values predicted by a simplified ammonia volatilization model [16]. Total measured losses were generally in close agreement with predictions. For example, predicted losses following applications of urine to a ryegrass-white clover pasture in Canterbury, New Zealand were 20.7% in summer and 22.4% in autumn and were highly correlated with measured losses of 21.5% and 24.4% respectively (r = 0.998).The model was also tested for instantaneous rate of ammonia gas loss at 33 discrete sampling times for the summer experiment. Correlations were again highly significant (r = 0.951 for urine and r = 0.885 for urea).The interception of urine solution by herbage and litter on the pasture surface is discussed and was shown to account for some of the discrepancies between measurements and predictions. Soil surface pH was confirmed as an important factor in determining the extent of ammonia gas loss, and the practicalities of measuring this parameter under field conditions are presented. It was concluded that the model offers the potential for predicting ammonia volatilization losses following urine or aqueous urea applications to short pasture in non-leaching, non-nitrifying environments.     

Ammonia losses from surface-applied urea as related to urea application rates,plant residue and calcium chloride addition

Volatile losses of NH₃ from surface-applied urea are known to decrease in the presence of soluble Ca-salts or with a decrease in easily decomposable organic matter content (EDOM), both of which influence urease activity. How these factors interact to affect NH₃ losses is not fully understood. Studies were conducted to determine the effect CaCl₂ in sand with varying rates of EDOM on NH₃ losses from surface applied urea. The same effects were examined on agricultural soils containing partially decomposed native organic matter (NOM). Determinations were made in the laboratory on field soils, sand free of organic matter and sand with known amounts of grass clippings (GC, EDOM). Low levels of GC in sand with low amounts of added urea resulted in little NH₃ loss. Ammonia loss increased as more N was applied at the low levels of GC. The loss was independent of urea application rates at high levels of GC. Ammonia losses were reduced more effectively at low EDOM and NOM in the presence of Ca. Incubation of sand with GC at low rates prior to urea addition increased NH₃ losses relative to high levels of non-incubated GC. For the above situation incubation for as high as 24 days resulted in equivalent NH₃ losses. The amount and state of decomposition of existing organic matter affected the degree of NH₃ loss from surface placed urea and its control by added Ca-salts. Microbial decomposition of EDOM, such as might occur in the spring prior to urea addition, led to greater NH₃ losses. Greater loss of NH₃ from urea might be an indication of a larger ureolytic microbial population leading to increased urease production.     

Ammonia volatilization from urea nitricphosphate and urea applied to the soil surface

Urea nitricphosphate (UNP) is an N-P fertilizer prepared by solubilizing phosphate ore with nitric acid and conditioning the product with urea. The product is acidic, and its nutrient analysis is 23-12-0. Urea makes up 74% of the N component of this material and the remainder comes from the nitrate added as nitric acid. In volatilization trials, UNP lost significantly less N than did urea in a noncalcareous soil (13 and 31% respectively). In calcareous soils the urea-N component of UNP exhibited loss patterns similar to those of urea. Soil pH remained stable at the center of the granule placement site during UNP hydrolysis, thereby reducing NH₃ loss, whereas the pH of the same soil treated with urea rose almost 1.9 units. The urea component of UNP appeared to diffuse from the center of the acidic microsite allowing hydrolysis to take place and permitting limited NH₃ volatilization to occur. UNP appears to be an attractive NP fertilizer in terms of nutrient analysis and resistance of the N component to volatile N losses as NH₃.     

Efficiency of N-(n-butyl) thiophosphoric triamide in retarding hydrolysis of urea and ammonia volatilization losses in a flooded sandy loam soil amended with organic materials

Using a forced-draft chamber technique, the suppression of NH3 volatilization losses by applying N-(n-butyl) thiophosphoric triamide (NBPT) was studied in an alkaline sandy loam soil amended with green manure or wheat straw. Applied urea was completely hydrolysed in 12, 8 and 6 days in unamended, green manure and wheat straw amended soil, respectively. By applying 0.5% (w/w of urea) NBPT, complete hydrolysis of urea was delayed up to 16 days in the unamended soil, whereas in wheat straw amended soil urea hydrolysis was completed by the 12th day even when it was treated with 2% NBPT. Applied at 1 or 2% level, NBPT delayed the NH3 volatilization to the 4th day after application of urea in green manure or wheat straw amended soil. Hydrolysis of urea was more effectively retarded by applying NBPT in the unamended soil than in soil amended with green manure or wheat straw. In the unamended soil, 7.1% of the applied urea was lost through NH3 volatilization. The losses were reduced to 1.2 and 0.7% by applying 0.5 and 1% NBPT, respectively. Enhanced NH3 volatilization caused by the green manure or wheat straw was counteracted by applying NBPT.     

Dynamics of ammonia volatilization from simulated urine patches and aqueous urea applied to pasture I. Field experiments

Ammonia (NH₃) volatilization losses from simulated sheep urine patches in a perennial ryegrass (Lolium perenne L.)/white clover (Trifolium repens L.) pasture in New Zealand were measured in the field during the summer, autumn and winter periods. An enclosure technique was used with microplots (23 cm diameter) receiving either sheep urine or aqueous urea at rates equivalent to 500 kg N ha^–1 and monitored continuously until measured losses decreased to 0.5% per day. Mean volatilization losses for urine treated plots were 22.2% of the applied N in summer, 24.6% in autumn and 12.2% in winter. Corresponding losses for the urea treated plots were 17.9%, 28.9% and 8.5%. Differences between these two N sources were not significant although the seasonal differences were significant (P 0.05). Changes in NH₃ gas fluxes were found to be related to measured changes in soil pH and air temperature. Two repeated applications of urine or aqueous urea to the same microplot resulted in significantly greater subsequent volatilization losses averaging 29.6% from the second and 37.5% from the third application.Most of the applied N was accounted for as either soil mineral N (NH ₄ ⁺ + NO ₃ ^- + NO ₂ ^- ) or NH_3(g) . Urea hydrolysis was rapid and obeyed the first order kinetics during the 24 hours following application. Calculated half-lives of urea in urine and aqueous urea were significantly different and were 3.0 and 4.7 h respectively during the summer and 4.7 and 12.0 h during the autumn.Implications of the results obtained to practical field situation together with the efficacy of the enclosure technique for measuring volatilization losses are discussed.     

The influence of soil properties on the effectiveness of phenylphosphorodiamidate (PPD) in reducing ammonia volatilization from surface applied urea

Urea can be an inefficient N source due to rapid hydrolysis by soil urease leading to NH₃ volatilization. The current study investigated the effect of the urease inhibitor phenylphosphorodiamidate (PPD) incorporated at two concentrations (0.5% and 1% w/w) within the fertilizer granule on NH₃ volatilization from surface applied urea. The daily rates of NH₃ loss from 20 soils of widely differing properties from Northern Ireland were measured over 14 days using ventilated enclosures under simulated spring conditions. Cumulative loss rates were calculated and fitted to a logistic model from which total NH₃ loss (Amax) and the time to maximum rate of loss (Tmax) were determined. Stepwise multiple linear regression analysis related the effectiveness of PPD in reducing NH₃ volatilization from urea to soil properties.The total cumulative loss of ammonia from unamended urea varied from 0.37 to 29.2% depending on soil type. Ammonia volatilization appeared to be greatest on a soil with a high pH (R² = 0.65), a low titratable acidity (TA) (R² = 0.63) and a soil that was drying out (R² = 0.50). Soil pH was negatively correlated with TA (r = –0.826, P < 0.001) suggesting that soils with a low TA may have received recent lime. Including cation exchange capacity (CEC) and % N as well as pH-KCl in the multiple linear regression equation explained 86% of the variance.The effectiveness of PPD in reducing Amax varied between 0% to 91% depending on soil type, the average over all 20 soils being 30 and 36% for 0.5% and 1% PPD respectively. The most important soil properties influencing the effectiveness of the urease inhibitor were soil pH-H₂O and TA accounting for 33% and 29% of the variance respectively. PPD was less effective on a soil with a high pH and low TA. These were the soil conditions that led to high NH₃ volatilization from unamended urea and may explain why PPD had limited success in reducing ammonia loss on these soils. Multiple linear regression analysis indicated that 75% of the variation in the % inhibition of NH₃ loss by PPD could be significantly accounted for by pH-H₂O, initial soil NO ₃ ^- -N concentration, % moisture content and % moisture loss.The delay in Tmax by PPD ranged from 0.19 to 7.93 days, the average over all 20 soils being 2.5 and 2.8 days for 0.5% and 1% PPD respectively. TA, % moisture content, urease activity and CEC were soil properties that significantly explained 83% of the variation in the % delay in Tmax by PPD in multiple linear regression analysis. However, none of these soil properties were significant on their own. As urea hydrolysis occurs rapidly in soil, delaying Tmax under field conditions would increase the chance of rain falling to move the urea below the soil surface and reduce NH₃ volatilization. A urease inhibitor should be more effective than PPD on soils with a high pH and low TA to be successful in reducing high NH₃ losses.     

Estimating ammonia volatilization from unsaturated urea fertilized and urine affected soils by an indirect method

An indirect method for evaluating the emission of ammonia from urea-fertilized upland crops or urine-affected pastures, without affecting the plant's environment, was evaluated at Yanco, N.S.W., Australia and near Lincoln University, New Zealand. The parameters measured were the ammoniacal nitrogen concentration, pH and temperature in the aqueous phase at the soil's surface, and windspeed at a reference height. The combined effect of these influences on volatilization rate were incorporated into a linear relationship of the form F =k u _z 0, where F is the vertical flux of ammonia, determined by a micrometeorological method,u _z is the wind speed at some reference height above the soil,0 is the ammonia concentration in equilibrium with the liquid phase (calculated from the ammoniacal nitrogen concentration, pH and temperature) andk is a proportionality constant. Strong linear relationships of this kind were found for the data sets from both experiments. The respective correlation coefficients for the relationships at the two sites were 0.870 and 0.879, and the respective k values were 6.3 × 10^–5 and 7.5 × 10^–5. The field measurements require little in the way of specialized equipment (e.g. flat - surface pH electrode, ammonia electrode, anemometer) and are comparatively easy to carry out. The results suggest that with some further refinement, this technique could achieve application in the calculation of ammonia losses from small plots in the field.     

Factors controlling ammonia loss from trash covered sugarcane fields fertilized with urea

Ammonia losses following surface applications of urea to trash covered sugar cane fields were investigated in four climatic zones of tropical Queensland. Volatilization of ammonia and evaporation of water were determined by micrometeorological techniques. The results showed that the pattern, rate and extent of ammonia loss were controlled by the availability of water in the trash and its evaporation. Water added by dewfall, rainfall or condensation of evaporated soil moisture dissolved some of the urea and allowed it to be hydrolyzed to ammonia by the urease enzyme in the sugarcane residues; when the water evaporated, ammonia was lost to the atmosphere.In the dry climatic zone, where no rain or dew fell, water addition to the trash by condensation of evaporated soil moisture was not sufficient to dissolve much urea so very little ammonia was lost. In the cool and warm moist zones, small additions of water to the trash from dew, light rain and condensation maintained a slow but steady pattern of ammonia loss over a period of six weeks and resulted in losses of 32% and 39% of the applied nitrogen. At the site in the wet zone, heavy rainfall apparently washed the urea from the trash layer into the soil and limited ammonia loss to 17% of the applied nitrogen.Substitution of ammonium sulfate for urea reduced ammonia loss to less than 1.8% of the applied nitrogen.     

Interdependence of ammonia volatilization and nitrification in arid soils

The effect of applied-N (urea) on interdependence of ammonia volatilization and nitrification was studied in twelve arid soils varying mainly in soil texture and CaCO₃. Ammonia volatilization from applied urea was observed only above a threshold N concentration in soil (V_i). Values of V_i ranged from 50 in sandy soils to 250 g N g^-1 in loamy and clay loam soils. Soils with higher CaCO₃ showed lower values of V_i. Concentration of applied-N in soils, in relation to V_i determined its transformation pathway(s). Below V_i, all of the applied-N was nitrified in all soils with a delayed nitrification period ranging from 0 to 5 days. Above V_i, ammonia volatilization was first to start. This reduced NH₄ ⁺ concentration in soil and nitrification started later after the delay period was over. Duration of delay period increased with applied-N, sand content and CaCo₃. Often 80% or more of the total ammonia, volatilized during the delay period. NH₄ ⁺ concentration in soil at which volatilization ended was generally higher than V_i. It was concluded that both ammonia volatilization and nitrification were interdependent only if concentration of applied N was more than V_i. Above V_i only one process predominated at a time as volatilization stopped soon after the start of nitrification even if NH₄ concentration in soil was sufficient to sustain both processes.