Salinity and nitrogen mineralization in soil

A laboratory study determined the effects of salinity on ammonification, nitrification and mineral N accumulation in incubated soils. NH⁺₄-N, NO^?₂-N and NO^?₃-N were measured periodically for 102 days in unamended soil of varying salinity and in soil amended with farm compost, mustard oil cake or urea. Increased salinity progressively retarded ammonification but did not suppress it completely. Nitrification was retarded, suppressed or inhibited completely by salinity, the effect depended on both the amount of salt and the type of amendment added to the soil. The amount of mineral N that accumulated generally decreased with increased salinity.     

The potential of using 15N natural abundance in changing ammonium-N and nitrate-N pools for studying in situ soil N transformations

Purpose

This study examined the usefulness of ¹⁵N natural abundance (δ¹⁵N) with in situ core incubation to quantify the predominant N transformation processes in a natural suburban forest of subtropical Australia, which was subjected to prescribed burning.

Materials and methods

In situ core incubation for 3 days with 20 ml water, or 160.79 ml of 60 mg L^?1 NO₃^?-N surface application, and in situ core with 160.79 ml water but without incubation were set up in Toohey forest for sampling three times as before (once) and after (twice) a prescribed burning. The δ¹⁵N of NH₄⁺-N and NO₃^?-N in the top 5 cm soil before and after the incubation, and δ¹⁵N of NO₃^?-N in the 5–10 cm soil before incubation were compared with each other to examine the soil N mineralisation, nitrification, denitrification, and nitrate leaching processes.

Results and discussion

The significant decrease in δ¹⁵N of NH₄⁺-N after incubation under 20 ml water treatment was ascribed to soil N mineralisation, and the significant decrease in δ¹⁵N of NH₄⁺-N and significant increase in δ¹⁵N of NO₃^?-N after incubation with elevated water and nitrate inputs were associated with N mineralisation and nitrification, respectively, 2 months after the burning. The 160.79 ml water treatment also triggered nitrification in the baseline soil cores in both samplings after the burning. Water was crucial to stimulate soil N mineralisation and nitrification, but excessive water depleted labile N pools and reduced N mineralisation and nitrification. Burning effects were hard to separate from the seasonal impacts on soil N cycling processes.

Conclusions

The δ¹⁵N in soil mineral N pools was sensitive to indicate soil N mineralisation and nitrification processes. Soil water and labile N were determining factors for N transformations in the soil. It is suggested that δ¹⁵N combined with soil inorganic N concentrations and net N transformation rates could be used to identify primary N transformation processes. More frequent samplings would be needed to differentiate burning impacts from the seasonal impacts on soil N cycling processes.

     

Release of mineral N from soils: Influence of inhibitors of nitrification

Nitrification inhibitors (N-Serve, ATC, and CS₂) were added to soils without N fertilizers. While the amount of nitrification of NH₄⁺-N was reduced, so was the amount of ammonification of soil N. This effect was greater with ATC and CS₂ than with N-Serve. In three field experiments, the application in the fall of ATC at 22 kg ha^?1 mixed into the soil reduced the loss of soil mineral N in early spring. Apparently, the inhibition suppressed both ammonification and nitrification of soil N during the winter, and consequently there was less NO^?₃ in soil when the wet period occurred in the spring.     

Mineralization of nitrogen in fertilizer-acidified lime-amended soils

Summary The application of NH _inf4 ^su+ -based fertilizers to soils slowly lowers soil pH, which in turn decreases nitrification rates. Under these conditions nitrification and N mineralization may be reduced. We therefore investigated the impact of liming fertilizer-acidified soils on nitrification and N mineralization. Soil samples were collected in the spring of 1987 from a field experiment, initiated in 1980, investigating N, tillage, and residue management under continuous corn (Zea mays L.). The pH values (CaCl₂) in the surface soil originally ranged from 6.0 to 6.5. After 6 years the N fertilizer and tillage treatments had reduced the soil pH to values that ranged between 3.7 and 6.2. Incubation treatments included two liming rates (unlimed or SMP-determined lime requirement), two ¹⁵N-labeled fertilizer rates (0 or 20 g N m^-2), and three replicates. Field-moist soil was mixed with lime and packed by original depth into columns. Labeled-¹⁵N ammonium sulfate in solution was surface-applied and columns were leached with 1.5 pore volumes of deionized water every 7 days over a 70-day period. Nitrification occurred in all pH treatments, suggesting that a ferilizer-acidified soil must contain a low-pH tolerant nitrifier population. Liming increased soil pH values (CaCl₂) from 3.7 to 6.2, and increased by 10% (1.5 g N m^-2) the amount of soil-derived NO₃ ^--N that moved through the columns. This increase was the result of enhanced movement of soil-derived NO₃ ^--N through the columns during the first 14 days of incubation. After the initial 14-day period, the limed and unlimed treatments had similar amounts of soil N leaching through the soil columns. Lime increased the nitrification rates and stimulated the early movement of fertilizer-derived NO₃ ^--N through the soil.     

Effect of sodium chloride on CO2 evolution,ammonification, and nitrification in a Sassafras sandy loam

Sodium chloride, at rates up to 100 mg g^?1, was added to a Sassafras sandy loam amended with finely-ground alfalfa to determine the effect of NaCl on CO₂ evolution, ammonification, and nitrification in a 14-week study. A NaCl concentration of 0.25 mg g^?1 significantly reduced CO₂ evolution by 16% in unamended soil and 5% in alfalfa-amended soil. Increasing NaCl progressively reduced CO₂ evolution, with no CO₂ evolved from the soil receiving 100 mg NaCl g^?1. A 0.50 mg NaCl g^?1 rate was required before a significant reduction in decomposition of the alfalfa occurred. The NO^?₂-N + NO^?₃-N content of the soil was significantly reduced from 40 to 37 μg g^?1 at 0 and 0.25 mg NaCl g^?1, respectively in the unamended soil. In the alfalfa amended soil, nitrification was significantly reduced at 5 mg NaCl g^?1. At 10 mg NaCl g^?1, nitrification was completely inhibited, there being only 6 and 2 μg NO^?₂-N + NO^?₃-N g^?1 in the alfalfa amended and unamended soil, respectively. In the alfalfa amended soil NH⁺₄-N accumulated from 6 μg g^?1 at the 0 NaCl rate to a maximum of 54 μg g^?1 with 25 mg NaCl g^?1. These higher NH⁺₄-N values resulted in a 0.5 unit increase in the pHw over that of the 0 NaCl rate in the alfalfa amended soil. At NaCl concentrations above 25 mg g^?1 there was a reduction in NH⁺₄-N. The addition of alfalfa to the soil helped to alleviate the adverse affects of NaCl on CO₂ evolution and nitrification.     

Nitrification in two coniferous forest soils after different fertilization treatments

The effects of seven different fertilization treatments on nitrification in the organic horizons of a Myrtillus-type (MT) and a Calluna-type pine forest in southern Finland were studied. No (NO^?₃ + NO^?₂)-N accumulated in unfertilized soils during 6 weeks at 14 or 20°C in the laboratory. Net nitrification was stimulated by urea in both soils (but more in the MT pine forest soil) and to a lesser degree by wood ash but not by ammonium nitrate or nitroform (ureaformaldehyde). Nitrification was not detected in nitroform fertilized soils although ammonium accumulation was high during incubation. In the MT pine forest soil, net nitrification appeared to be stimulated by apatite, biotite and micronutrients. Nitrapyrin inhibited nitrification indicating that it was carried out by autotrophic nitrifiers. In the urea-fertilized MT pine forest soil, nitrification took place at an incubation temperature of 0°C. Accumulation of (N0^?₃ + NO^?₂)-N was highest in soil sampled at < 10°C.     

Nitrogen Recovery and Transformation from a Surface or Sub-Surface Application of Controlled-Release Fertilizer on a Sandy Soil

ABSTRACT

Controlled-release fertilizers (CRF) are used to reduce leaching of nutrients, especially nitrate-nitrogen (NO₃ ^?-N) to groundwater, caused mainly by application of soluble N fertilizers to sandy soils in Florida. A leaching column study was conducted to evaluate N release and transformation from a CRF (CitriBlen) over a 16-week period when it was applied on the soil surface or incorporated into the soil. When one pore volume of water was applied to column weekly or biweekly, the CRF released urea-N slowly over time with three peaks of release on 3–4, 8, and 12 week after application. Both ammonium-nitrogen (NH₄ ⁺-N) and NO₃ ^?-N were leached in large amounts on week 2, likely from soluble forms of N. Cumulatively, the most leached N at the end of study was in the NH₄ ⁺ form, followed by the NO₃ ^? form. The sum of all N forms leached and volatilized accounted for 53–69% of total N applied. Total N recovery was 70% and 93% of total N applied for surface and sub-surface application of the fertilizer, respectively. It was indicated that the better recovery rate found with sub-surface application may have been due to minimized N loss by volatilization. Sub-surface application of fertilizer resulted in more than three times NH₄ ⁺-N remained in soil, compared with surface application. On average for both application treatments throughout 16-week period, 5.8 h was required for ammonification and 4.7 d for nitrification to occur after N release from the fertilizer. Characterization of CRFs for specific soil type, leaching volume and cycle, and application manner as well as knowledge of N requirement of the crop will allow for the Best Management Practices of these fertilizers, thus obtaining optimum yields and minimizing nutrient losses from CRFs.     

Recovery of soil organic matter,organic matter turnover and nitrogen cycling in a post-mining forest rehabilitation chronosequence

Recovery of soil organic matter, organic matter turnover and mineral nutrient cycling is critical to the success of rehabilitation schemes following major ecosystem disturbance. We investigated successional changes in soil nutrient contents, microbial biomass and activity, C utilisation efficiency and N cycling dynamics in a chronosequence of seven ages (between 0 and 26 years old) of jarrah (Eucalyptus marginata) forest rehabilitation that had been previously mined for bauxite. Recovery was assessed by comparison of rehabilitation soils to non-mined jarrah forest references sites. Mining operations resulted in significant losses of soil total C and N, microbial biomass C and microbial quotients. Organic matter quantity recovered within the rehabilitation chronosequence soils to a level comparable to that of non-mined forest soil. Recovery of soil N was faster than soil C and recovery of microbial and soluble organic C and N fractions was faster than total soil C and N. The recovery of soil organic matter and changes to soil pH displayed distinct spatial heterogeneity due to the surface micro-topography (mounds and furrows) created by contour ripping of rehabilitation sites. Decreases in the metabolic quotient with rehabilitation age conformed to conceptual models of ecosystem energetics during succession but may have been more indicative of decreasing C availability than increased metabolic efficiency. Net ammonification and nitrification rates suggested that the low organic C environment in mound soils may favour autotrophic nitrifier populations, but the production of nitrate (NO₃^?) was limited by the low gross N ammonification rates (≤1 μg N g^?1 d^?1). Gross N transformation rates in furrow soils suggested that the capacity to immobilise N was closely coupled to the capacity to mineralise N, suggesting NO₃^? accumulation in situ is unlikely. The C:N ratio of the older rehabilitation soils was significantly lower than that of the non-mined forest soils. However, variation in ammonification rates was best explained by C and N quantity rather than C:N ratios of whole soil or soluble organic matter fractions. We conclude that the rehabilitated ecosystems are developing a conservative N cycle as displayed by non-mined jarrah forests. However, further investigation into the control of nitrification dynamics, particularly in the event of further ecosystem disturbance, is warranted.     

Nitrogen mineralisation in the soil of indigenous oak and pine plantation forests in a Mediterranean environment

Nitrogen mineralisation in soils of various forest sites (pine plantation, natural and thinned oak) at Uluda? University campus in Bursa, Turkey was investigated continuously over a year by the field incubation method. Net nitrogen mineralisation and nitrification rates varied depending on sampling dates. Although nitrogen mineralisation and nitrification rates increased in the spring and summer months, there was no seasonal variation in the soils of the examined forests. Annual net nitrate (NO₃^?–N) accumulation in the upper soil layer (0–5 cm) was higher in Oak I and Oak II (14 kg ha y^?1 and 12 kg ha y^?1) than in the pine plantation (8 kg ha y^?1). While annual net NO₃^?–N accumulation (0–5 cm) varied between the oak forests (possibly due to forest management practices), annual net N_min values were similar in these forests. No significant correlation was found between the examined soil parameters and net nitrification and mineralisation rates in the soils (P > 0.05). These results indicate that tree species and forest management practices play important roles in N cycling in forest ecosystems.     

Clinoptilolite Zeolite Influence on Nitrogen in a Manure-Amended Sandy Agricultural Soil

Zeolite minerals may improve nitrogen availability to plants in soil and reduce losses to the environment. A study was conducted to determine the influence of clinoptilolite (CL) on nitrogen (N) mineralization from solid dairy manure (224 kg N ha^?1) in a sandy soil. Clinoptilolite was added to soil at six rates (0 to 44.8 Mg CL ha^?1), each sampled during 11 sampling dates over a year. Over time, nitrate (NO₃)-N increased, ammonium (NH₄)-N decreased, but total inorganic N increased. Clinoptilolite did not influence the nitrification rates of initial manure NH₄-N or mineralization of organic N (ON) over time. It is possible that adsorption of manure-derived potassium (K) outcompeted the NH₄-N for CL exchange sites. The ON concentration was constant up to 84 days and then decreased by approximately 18% over the remaining time of the study across all treatments. Clinoptilolite use in this sandy soil did not alter mineralization of N from dairy manure.     

Wheat straw and its biochar had contrasting effects on soil C and N cycling two growing seasons after addition to a Black Chernozemic soil planted to barley

Application of crop residues and its biochar produced through slow pyrolysis can potentially increase carbon (C) sequestration in agricultural production systems. The impact of crop residue and its biochar addition on greenhouse gas emission rates and the associated changes of soil gross N transformation rates in agricultural soils are poorly understood. We evaluated the effect of wheat straw and its biochar applied to a Black Chernozemic soil planted to barley, two growing seasons or 15 months (at the full-bloom stage of barley in the second growing season) after their field application, on CO₂ and N₂O emission rates, soil inorganic N and soil gross N transformation rates in a laboratory incubation experiment. Gross N transformation rates were studied using the ¹⁵N isotope pool dilution method. The field experiment included four treatments: control, addition of wheat straw (30 t ha^?1), addition of biochar pyrolyzed from wheat straw (20 t ha^?1), and addition of wheat straw plus its biochar (30 t ha^?1 wheat straw + 20 t ha^?1 biochar). Fifteen months after their application, wheat straw and its biochar addition increased soil total organic C concentrations (p?=?0.039 and <0.001, respectively) but did not affect soil dissolved organic C, total N and NH₄ ⁺-N concentrations, and soil pH. Biochar addition increased soil NO₃ ^?-N concentrations (p?=?0.004). Soil CO₂ and N₂O emission rates were increased by 40 (p?p?=?0.03), respectively, after wheat straw addition, but were not affected by biochar application. Straw and its biochar addition did not affect gross and net N mineralization rates or net nitrification rates. However, biochar addition doubled gross nitrification rates relative to the control (p?2 and N₂O emissions and enhance soil C sequestration. However, the implications of the increased soil gross nitrification rate and NO₃ ^?-N in the biochar addition treatment for long-term NO₃ ^?-N dynamics and N₂O emissions need to be further studied.     

Impact of nitrogen and phosphorus additions on soil gross nitrogen transformations in a temperate desert steppe

Nutrient addition has a significant impact on plant growth and nutrient cycling. Yet, the understanding of how the addition of nitrogen (N) or phosphorus (P) significantly affects soil gross N transformations and N availability in temperate desert steppes is still limited. Therefore, a ¹⁵N tracing experiment was conducted to study these processes and their underlying mechanism in a desert steppe soil that had been supplemented with N and P for 4 years in northwestern China. Soil N mineralization was increased significantly by P addition, and N and P additions significantly promoted soil autotrophic nitrification, rather than NH₄⁺-N immobilization. The addition of N promoted dissimilatory NO₃⁻ reduction to NH₄⁺, while that of P inhibited it. Soil NO₃⁻-N production was greatly increased by N added alone and by that of N and P combined, while net NH₄⁺-N production was decreased by these treatments. Soil N mineralization was primarily mediated by pH, P content or organic carbon, while soil NH₄⁺-N content regulated autotrophic nitrification mainly, and this process was mainly controlled by ammonia-oxidizing bacteria rather than archaea and comammox. NH₄⁺-N immobilization was mainly affected by functional microorganisms, the abundance of narG gene and comammox Ntsp-amoA. In conclusion, gross N transformations in the temperate desert steppe largely depended on soil inorganic N, P contents and related functional microorganisms. Soil acidification plays a more key role in N mineralization than other environmental factors or functional microorganisms.     

Identifying the Growth Limiting Physiochemical Parameter for Chives Grown in Biologically Treated Graywater

Plants can play an important role in wastewater treatment and water reuse in terrestrial and space systems. Chive growth in biologically treated graywater, simulating the anticipated early planetary base graywater, was evaluated in this study for NASA. Phytotoxicity due to physiochemical parameters such as ammonium-nitrogen (NH₄ ⁺-N), nitrite-nitrogen (NO₂ ^?-N), pH, and sodium (Na⁺) was assessed using a series of hydroponic experiments in an environmentally controlled growth chamber. Nitrification in wastewater was observed in all graywater treatments, which converted NO₂ ^?-N (a toxic form of nitrogen) and NH₄ ⁺-N (toxic at high concentrations) to nitrate-nitrogen (NO₃ ^?-N) (preferred N form for plant uptake). Irrespective of the increase in the NO₃ ^–-N concentration due to nitrification, chives in the wastewater treatments typically had poor or no growth. The high levels of Na⁺ present in the graywater treatments affected potassium uptake and may have affected other nutrient uptake. The impact of nitrification on wastewater pH and NO₂ ^?-N toxicity is believed to be the critical factor affecting chive growth and may hinder the use high nitrogen waste streams for plant growth unless NO₂ ^?-N concentrations are controlled during biological treatment of graywater.     

The effects of biocidal treatments on metabolism in soil—VI. Fumigation with carbon disulphide

Used in high concentration as a soil fumigant, CS₂ was broadly similar to CHCl₃ in its effects on metabolism in soil; the amount of N mineralised in 10 days increased roughly 10-fold. the O₂ consumption almost tripled and the evolution of CO₂ more than doubled. However, the effects of CS₂ were consistently slightly less than those of CHCl₃.Used at low concentration (10 μg.g^?1 soil) on a soil rich in organic matter (2.93% organic C), CS₂ stopped nitrification completely, almost without other effect on soil respiration and mineralisation of N. In contrast, when used on a poorer soil (1.07% organic C) even 10 μgCS₂.g_?1 soil was sufficient to cause a detectable increase in both respiration and mineralisation of N, in addition to stopping nitrification.     

Nitrate Transformation and N2O Emission in a Typical Intensively Managed Calcareous Fluvaquent Soil: A 15-Nitrogen Tracer Incubation Study

A 56-day aerobic incubation experiment was performed with 15-nitrogen (N) tracer techniques after application of wheat straw to investigate nitrate-N (NO₃-N) immobilization in a typical intensively managed calcareous Fluvaquent soil. The dynamics of concentration and isotopic abundance of soil N pools and nitrous oxide (N₂O) emission were determined. As the amount of straw increased, the concentration and isotopic abundance of total soil organic N and newly formed labeled particulate organic matter (POM-N) increased while NO₃-N decreased. When ¹⁵NO₃-N was applied combined with a large amount of straw at 5000 mg carbon (C) kg^?1 only 1.1 ± 0.4 mg kg^?1 NO₃-N remained on day 56. The soil microbial biomass N (SMBN) concentration and newly formed labeled SMBN increased significantly (P < 0.05) with increasing amount of straw. Total N₂O-N emissions were at levels of only micrograms kg^?1 soil. The results indicate that application of straw can promote the immobilization of excessive nitrate with little emission of N₂O.     

Dicyandiamide application improved nitrogen use efficiency and decreased nitrogen losses in wheat-maize crop rotation in Loess Plateau

Inhibition of nitrification as a mitigation tool to abate nitrogen (N) losses and improve N use efficiency (NUE) is a promising technology. Nitrification inhibitor (dicyandiamide, DCD) was evaluated in two consecutive wheat-maize rotations (2015–2017), with two different N fertilizer levels applied in wheat (160, 220 kg N ha^?1) and maize (180, 280 kg N ha^?1). More NH₄⁺-N contents (101% and 102% in wheat and 74% and 73% in maize) and less NO₃^–-N contents (37% and 43% in wheat and 46% and 57% in maize) were observed at both N levels treated with DCD compared to without DCD. Higher pH, lower EC and reduced NO₃^–-N accumulation were the other benefits of DCD. The NO₃^–-N accumulation within the 0–200 cm soil profile was significantly less at both N levels with DCD (66 mg kg^?1 and 121 mg kg^?1) compared to without DCD (96 mg kg^?1 and 169 mg kg^?1). Application of DCD also improved the growth and yield in both crops. Increase in NUE from 38% to 49% in wheat and 27% to 33% in maize with DCD at higher N level was also observed. Overall, the effectiveness of DCD in retarding the nitrification process was higher in wheat than maize.     

Nitrification Inhibitor,Fertilizer Rate,and Temperature Effects on Nitrous Oxide Emission and Nitrogen Transformation in Loamy Sand Soil

An incubation study investigated the effects of nitrification inhibitors (NIs), dicyandiamide (DCD), and neem oil on the nitrification process in loamy sand soil under different temperatures and fertilizer rates. Results showed that NIs decreased soil nitrification by slowing the conversion of soil ammonium (NH₄⁺)-nitrogen (N) and maintaining soil NH₄⁺-N and nitrate (NO₃^?)-N throughout the incubation time. DCD and neem oil decreased soil nitrous oxide (N₂O) emission by up to 30.9 and 18.8%, respectively. The effectiveness of DCD on reducing cumulative soil N₂O emission and retaining soil NH₄⁺-N was inconsistently greater than that of neem oil, but the NI rate was less obvious than temperature. Fertilizer rate had a stronger positive effect on soil nitrification than temperature, indicating that adding N into low-fertility soil had a greater influence on soil nitrification. DCD and neem oil would be a potential tool for slowing N fertilizer loss in a low-fertility soil under warm to hot climatic conditions.     

Evidence that fungi can oxidize NH4+ to NO3− in a grassland soil

The contribution of bacteria and fungi to NH₄⁺ and organic N (N_org) oxidation was determined in a grassland soil (pH 6.3) by using the general bacterial inhibitor streptomycin or the fungal inhibitor cycloheximide in a laboratory incubation study at 20°C. Each inhibitor was applied at a rate of 3 mg g^?1 oven‐dry soil. The size and enrichment of the mineral N pools from differentially (NH₄¹⁵NO₃ and ¹⁵NH₄NO₃) and doubly labelled (¹⁵NH₄¹⁵NO₃) NH₄NO₃ were measured at 3, 6, 12, 24, 48, 72, 96 and 120 hours after N addition. Labelled N was applied to each treatment, to supply NH₄⁺‐N and NO₃^?‐N at 3.15 μmol N g^?1 oven‐dry soil. The N treatments were enriched to 60 atom % excess in ¹⁵N and acetate was added at 100 μmol C g^?1 oven‐dry soil, to provide a readily available carbon source. The oxidation rates of NH₄⁺ and N_org were analysed separately for each inhibitor treatment with a ¹⁵N tracing model. In the absence of inhibitors, the rates of NH₄⁺ oxidation and organic N oxidation were 0.0045 μmol N g^?1 hour^?1 and 0.0023 μmol N g^?1 hour^?1, respectively. Streptomycin had no effect on nitrification but cycloheximide inhibited the oxidation of NH₄⁺ by 89% and the oxidation of organic N by more than 30%. The current study provides evidence to suggest that nitrification in grassland soil is carried out by fungi and that they can simultaneously oxidize NH₄⁺ and organic N.     

Influence of the nitrification inhibitor DMPP on the community composition of ammonia-oxidizing bacteria at microsites with increasing distance from the fertilizer zone

The effect of the nitrification inhibitor 3,4-dimethylpyrazole phosphate (DMPP) on N transformations and composition of ammonia-oxidizing bacteria (AOB) communities was investigated at the centimeter scale in a microcosm experiment under laboratory conditions. After 28 days, samples were collected from soil treated with urea or urea and DMPP at increasing distance from the fertilizer zone; this distance ranged from 0 to 5 cm in both horizontal and vertical directions. The results showed that DMPP application significantly increased soil pH and NH ₄ ⁺ -N and mineral N (NH ₄ ⁺ -N, NO ₃ ^? -N, and NO ₂ ^? -N) concentrations but decreased (NO ₃ ^? + NO ₂ ^? )-N concentration, and such effect was decreased by increasing the distance from the fertilizer zone. Fingerprint profiles of denaturing gradient gel electrophoresis showed that the number of bands decreased by increasing the distance from the fertilizer zone due to decreasing NH ₄ ⁺ -N concentrations in the urea treatment. Compared to urea applied alone, DMPP application increased NH ₄ ⁺ -N concentrations and decreased AOB diversity from 0 to 3 cm but promoted diversity from 3 to 5 cm distance from the fertilizer zone. A phylogenetic analysis showed that AOB communities were dominated by Nitrosospira cluster 3. Therefore, the nitrification inhibitor DMPP modified the composition of AOB communities by increasing the distance from the fertilizer zone and this probably was related to the changes in soil pH and inorganic N concentration.     

Nitrogen transformation from three soil organic amendments in a sandy soil

Abstract

A sandy soil was amended with various rates (20 – 320 g air-dry weight basis of the amendments per kg of air-dry soil) of chicken manure (CM), sewage sludge (SS), and incinerated sewage sludge (ISS) and incubated for 100 days in a greenhouse at 15% (wt/wt) soil water content. At the beginning of incubation, NH₄-N concentrations varied from 50 – 280 mg kg^?1 in the CM amended soil with negligible amounts of NO₃-N. Subsequently, the concentration of NH₄-N decreased while that of NO₃-N increased rapidly. In soil amended with SS at 20 – 80 g kg^?1 rates, the NO₃-N concentration increased sharply during the first 20 days, followed by a slow rate of increase over the rest of the incubation period. However, at a 160 g kg^?1 SS rate, there were three distinct phases of NO₃-N release which lasted for160 days. In the ISS amended soil, the nitrification process was completed during the initial 30 days, and the concentrations of NH₄-N and NO₃-N were lower than those for the other treatments. The mineralized N across different rates accounted for 20 – 36%, 16 – 40%, and 26 – 50% of the total N applied as CM, SS, and ISS, respectively.