Evolution of dinitrogen and nitrous oxide from the soil to the atmosphere through rice plants

Summary It is commonly assumed that a large fraction of fertilizer N applied to a rice (Oryza sativa L.) field is lost from the soil-water-plant system as a result of denitrification. Direct evidence to support this view, however, is limited. The few direct field, denitrification gas measurements that have been made indicate less N loss than that determined by ¹⁵N balance after the growing season. One explanation for this discrepancy is that the N₂ produced during denitrification in a flooded soil remains trapped in the soil system and does not evolve to the atmosphere until the soil dries or is otherwise disturbed. It seems likely, however, that N₂ produced in the soil uses the rice plants as a conduit to the atmosphere, as does methane. Methane evolution from a rice field has been demonstrated to occur almost exclusively through the rice plants themselves. A field study in Cuttack, India, and a greenhouse study in Fort Collins, Colorado, were conducted to determine the influence of rice plants on the transport of N₂ and N₂O from the soil to the atmosphere. In these studies, plots were fertilized with 75 or 99 atom % ¹⁵N-urea and ¹⁵N techniques were used to monitor the daily evolution of N₂ and N₂O. At weekly intervals the amount of N₂+N₂O trapped in the flooded soil and the total-N and fertilized-N content of the soil and plants were measured in the greenhouse plots. Direct measurement of N₂+N₂O emission from field and greenhouse plots indicated that the young rice plant facilitates the efflux of N₂ and N₂O from the soil to the atmosphere. Little N gas was trapped in the rice-planted soils while large quantities were trapped in the unplanted soils. N losses due to denitrification accounted for only up to 10% of the loss of added N in planted soils in the field or greenhouse. The major losses of fertilizer N from both the field and greenhouse soils appear to have been the result of NH₃ volatilization.     

Soil N Losses by Denitrification Evaluated Using the 15N Tracer Method

Molecular nitrogen (N₂) and nitrous oxide (N₂O) generated by denitrification increase N losses in the soil–plant system. This study aimed to quantify N₂ and N₂O from potassium nitrate (K¹⁵NO₃) applied to soils with different textures and moisture contents in the absence and presence of a source of carbon (C) using the ¹⁵N tracer method. In the three soils used (sandy texture (ST), sandy clay loam texture (SCLT), and clayey texture (CT)), three moisture contents were evaluated (40%, 60%, and 80% of the water holding capacity (WHC)) with (D⁺) and without (D^?) dextrose added. The treatments received 100 mg N kg^?1 (KNO₃ with 23.24 atom% ¹⁵N). N₂ emissions occurred in all of the treatments, but N₂O emissions only occurred in the D⁺ treatment, showing increases with increasing moisture content. SCLT with 80% WHC in the D⁺ treatment exhibited the highest accumulated N emission (48.26 mg kg^?1). The ¹⁵N balance suggested trapping of the gases in the soil.     

高氮和NO2-对中亚热带森林土壤N2O和NO产生的影响

利用15N同位素标记方法,研究在两种水分条件即60％和90％ WHC下,添加硝酸盐(NH4NO3,N 300 mg kg-1)和亚硝酸盐(NaNO2,N 1 mg kg-1)对中亚热带天然森林土壤N2O和NO产生过程及途径的影响.结果表明,在含水量为60％ WHC的情况下,高氮输入显著抑制了N2O和NO的产生(p＜0.01);但当含水量增为90％ WHC后,实验9h内抑制N2O产生,之后转为促进.所有未灭菌处理在添加NO2-后高氮抑制均立即解除并大量产生N2O和NO,与对照成显著差异(p＜0.01),在60％ WHC条件下,这种情况维持时间较短(21 h),但如果含水量高(90％ WHC)这种情况会持续很长时间(2周以上),说明水分有效性的提高和外源NO2-在高氮抑制解除中起到重要作用.本实验中N2O主要来源于土壤反硝化过程,而且加入未标记NO2-后导致杂合的N2O(14N15NO)分子在实验21 h内迅速增加,表明这种森林土壤的反硝化过程可能主要是通过真菌的“共脱氮”来实现,其贡献率可多达80％以上.Spearman秩相关分析表明未灭菌土壤NO的产生速率与N2O产生速率成显著正相关性(p＜0.05),土壤含水量越低二者相关性越高.灭菌土壤添加NO2-能较未灭菌土壤产生更多的NO,但却几乎不产生N2O,表明酸性土壤的化学反硝化对NO的贡献要大于N2O.     

Dinitrogen and N2O emissions in arable soils: Effect of tillage, N source and soil moisture

A laboratory investigation was performed to compare the fluxes of dinitrogen (N₂), N₂O and carbon dioxide (CO₂) from no-till (NT) and conventional till (CT) soils under the same water, mineral nitrogen and temperature status. Intact soil cores (0-10 cm) were incubated for 2 weeks at 25 °C at either 75% or 60% water-filled pore space (WFPS) with ¹⁵N-labeled fertilizers (100 mg N kg⁻¹ soil). Gas and soil samples were collected at 1-4 day intervals during the incubation period. The N₂O and CO₂ fluxes were measured by a gas chromatography (GC) system while total N₂ and N₂O losses and their ¹⁵N mole fractions in the soil mineral N pool were determined by a mass spectrometer. The daily accumulative fluxes of N₂ and N₂O were significantly affected by tillage, N source and soil moisture. We observed higher (P<0.05) fluxes of N₂+N₂O, N₂O and CO₂ from the NT soils than from the CT soils. Compared with the addition of nitrate (NO₃⁻), the addition of ammonium (NH₄⁺) enhanced the emissions of these N and C gases in the CT and NT soils, but the effect of NH₄⁺ on the N₂ and/or N₂O fluxes was evident only at 60% WFPS, indicating that nitrification and subsequent denitrification contributed largely to the gaseous N losses and N₂O emission under the lower moisture condition. Total and fertilizer-induced emissions of N₂ and/or N₂O were higher (P<0.05) at 75% WFPS than with 60% WFPS, while CO₂ fluxes were not influenced by the two moisture levels. These laboratory results indicate that there is greater potential for N₂O loss from NT soils than CT soils. Avoiding wet soil conditions (>60% WFPS) and applying a NO₃⁻ form of N fertilizer would reduce potential N₂O emissions from arable soils.     

Incomplete Acetylene Inhibition of Nitrous Oxide Reduction in Potential Denitrification Assay as Revealed by using 15N-Nitrate Tracer

One lake sediment and three soils for rice production were used to test the effectiveness of inhibiting of nitrous oxide (N₂O) reduction to dinitrogen gas (N₂) by acetylene (C₂H₂) using ¹⁵N tracer. Regardless of the sources of the samples, results show that in presence of C₂H₂, significant isotopic enrichment of ¹⁵N of N₂ was found at end of a typical denitrification assay. The δ¹⁵N of N₂ value increased from 0‰ to 7.8–19.3‰ and 7.5–10.6‰ for the treatment with addition of 0.05 and 0.2 mg ¹⁵N nitrate, respectively. Such ¹⁵N enrichment can be interpreted as N₂ formation accounting for 15.3% and 2.5% of the total added N in these two treatments, respectively. Nitrous oxide accumulation in presence of C₂H₂ could not account for the total added N. The result indicates incomplete inhibition of N₂O reduction to N₂ by C₂H₂ in denitrification when N₂O reduction enzyme is developed.     

The N2O product ratio of nitrification and its dependence on long-term changes in soil pH

The contribution of nitrification to the emission of nitrous oxide (N₂O) from soils may be large, but its regulation is not well understood. The soil pH appears to play a central role for controlling N₂O emissions from soil, partly by affecting the N₂O product ratios of both denitrification (N₂O/(N₂+N₂O)) and nitrification (N₂O/(NO₂⁻+NO₃⁻). Mechanisms responsible for apparently high N₂O product ratios of nitrification in acid soils are uncertain. We have investigated the pH regulation of the N₂O product ratio of nitrification in a series of experiments with slurries of soils from long-term liming experiments, spanning a pH range from 4.1 to 7.8. ¹⁵N labelled nitrate (NO₃⁻) was added to assess nitrification rates by pool dilution and to distinguish between N₂O from NO₃⁻ reduction and NH₃ oxidation. Sterilized soil slurries were used to determine the rates of chemodenitrification (i.e. the production of nitric oxide (NO) and N₂O from the chemical decomposition of nitrite (NO₂⁻)) as a function of NO₂⁻ concentrations. Additions of NO₂⁻ to aerobic soil slurries (with ¹⁵N labelled NO₃⁻ added) were used to assess its potential for inducing denitrification at aerobic conditions. For soils with pH?5, we found that the N₂O product ratios for nitrification were low (0.2-0.9‰) and comparable to values found in pure cultures of ammonia-oxidizing bacteria. In mineral soils we found only a minor increase in the N₂O product ratio with increasing soil pH, but the effect was so weak that it justifies a constant N₂O product ratio of nitrification for N₂O emission models. For the soils with pH 4.1 and 4.2, the apparent N₂O product ratio of nitrification was 2 orders of magnitude higher than above pH 5 (76‰ and 14‰). This could partly be accounted for by the rates of chemodenitrification of NO₂⁻. We further found convincing evidence for NO₂⁻-induction of aerobic denitrification in acid soils. The study underlines the role of NO₂⁻, both for regulating denitrification and for the apparent nitrifier-derived N₂O emission.     

Nitrate removal from drained and reflooded fen soils affected by soil N transformation processes and plant uptake

Knowledge about nitrate transformation processes and how they are affected by different plants is essential in order to reduce the loss of valuable N fertiliser as well as to prevent environmental pollution due to nitrate leaching or N₂O emission after fertilisation or the reflooding of degraded fens with nitrate-containing municipal sewage. Therefore four microcosm ¹⁵N tracer experiments were performed to evaluate the effect of common wetland plants (Phalaris arundinacea, Phragmites australis) combined with different soil moisture conditions (from dry to reflooded) on nitrate turnover processes. At the end of experiment, the total formation of gaseous N compounds was calculated using the ¹⁵N balance method. In two experiments (wet and reflooded soil conditions) the N₂O and N₂ emissions were also directly determined.Our results show that in degraded fen soils, which process mainly takes place—denitrification or transformation into organic N compounds—is determined by the soil moisture conditions. Under dry soil moisture conditions (water filled pore space: 31%) up to 80% of the ¹⁵N nitrate added was transformed into organic N compounds. This transformation process is not affected by plant growth. Under reflooded conditions (water filled pore space: 100%), the total gaseous N losses were highest (77-95% of the ¹⁵N-nitrate added) and the transformation into organic N compounds was very low (1.8% of ¹⁵N nitrate added). Under almost all soil conditions plant growth reduced the N losses by 20-25% of the ¹⁵N nitrate added due to plant uptake. The N₂ emissions exceeded the N₂O emissions by a factor of 10-20 in planted soil, and as much as 30 in unplanted soil. In the treatments planted with Phragmites australis, N₂O emission was about two times higher than in the corresponding unplanted treatment. 15% of the N₂O and N₂ formed was transported via the Phragmites shoots from the soil into the atmosphere. By contrast, Phalaris arundinacea did not affect N₂O emissions and no emission via the shoots was observed.     

Evidence of N<Subscript>2</Subscript>O emission and gaseous nitrogen losses through nitrification-denitrification induced by rice plants (<Emphasis Type="Italic">Oryza sativa</Emphasis> L.)

A greenhouse experiment was conducted with a specially designed apparatus consisting of an upper and lower chamber where the treatment with rice was carried out (treatment 1). The apparatus also had a single chamber where treatment 2, without rice plants, was carried out. The scope of this study was to elucidate the influence of rice plant growth on gaseous N losses as N₂ and N₂O produced by nitrification-denitrification in a flooded soil fertilized with (NH₄)₂SO₄ (with 56.50 atom% ¹⁵N). Gas samples were withdrawn weekly and analyzed for (N₂ + N₂O)-¹⁵N losses by mass spectrometer and for N₂O by gas chromatograph. The gaseous (N₂ + N₂O)-¹⁵N losses of the treatment with rice plants were significantly (P =0.01) higher than those of the treatment without rice plants, as were the amounts of N₂O emitted. Rice plants facilitate the efflux of N₂ and N₂O from soil to atmosphere, as about half of the total gaseous ¹⁵N loss as N₂ and N₂O was found in the upper chamber. The proportion of N₂O-¹⁵N to (N₂ + N₂O)-¹⁵N in the upper chamber was 10.56%, much higher than that of the lower chamber in treatment 1 and the headspace of treatment 2.     

Nitrapyrin effectiveness in reducing nitrous oxide emissions decreases at low doses of urea in an Andosol

In the tropics,frequent nitrogen(N)fertilization of grazing areas can potentially increase nitrous oxide(N₂O)emissions.The application of nitrification inhibitors has been reported as an effective management practice for potentially reducing N loss from the soil-plant system and improving N use efficiency(NUE).The aim of this study was to determine the effect of the co-application of nitrapyrin(a nitrification inhibitor,NI)and urea in a tropical Andosol on the behavior of N and the emissions of N₂O from autotrophic and heterotrophic nitrification.A greenhouse experiment was performed using a soil(pH 5.9,organic matter content 78 g kg^-1,and N 5.6 g kg^-1)sown with Cynodon nlemfuensis at 60%water-filled pore space to quantify total N₂O emissions,N₂O derived from fertilizer,soil ammonium(NH₄⁺)and nitrate(NO₃^-),and NUE.The study included treatments that received deionized water only(control,NI).No significant differences were observed in soil NH₄⁺content between the UR and UR+NI treatments,probably because of soil mineralization and NO₃^-produced by heterotrophic nitrification,which is not effectively inhibited by nitrapyrin.After 56 d,N₂O emissions in UR(0.51±0.12 mg N₂O-N concluded that the soil organic N mineralization and heterotrophic nitrification are the main processes of NH₄⁺and NO₃^-production.Additionally,it was found that N₂O emissions were partially a consequence of the direct oxidation of the soil's organic N via heterotrophic nitrification coupled to denitrification.Finally,the results suggest that nitrapyrin would likely exert significant mitigation on N₂O emissions only if a substantial N surplus exists in soils with high organic matter content.     

Denitrification in the rooting zone of cropped soils with regard to methodology and climate: A review

Summary Denitrification N losses can be determined by three methods. The first is by estimating the non-recovery of ¹⁵ N-labelled compounds (¹⁵N-balance method). Using this method, denitrification losses are deduced from the balance of an N budged (¹⁵N-labeled fertilizer), having accounted for transformations in soil, plant uptake, and leaching losses. The evolution of gaseous N from native soil N is not taken into account by this procedure. Studies on arable land with annual crops in the temperate zone have shown that of the fertilizer N applied, about 20–500% (10–70 kg N^* ha^–1) is not recovered at the end of the growth period. The second method of determining denitrification N losses is by in situ field measurement of ¹⁵ N ₂ and ¹⁵ N ₂ O production. Under this procedure, ¹⁵N-enriched N is applied to a plot and the denitrification N losses are determined by covering the soil. The method allows a quantitative estimate of the relative contributions to the emitted gas by both the original enriched source and the native soil N. N-evolution rates measured on arable land under a temperate climate are approximately the same order of magnitude as the N losses estimated by the non-recovery of ¹⁵ N method. The third measuring procedure is based on the acetylene inhibition phenomenon. This principle uses the inhibition of bacterial N₂O reduction to N₂ in the presence of acetylene (C₂H₂). The methoddetermines the denitrification of all NO₃ ^–-N irrespective of its source. Measurements on classical crop production systems show maximum N losses in the temperate climate of about 20–30 kg N^* ha^–1 during the growth period of annual crops. A similar level of denitrification is estimated for grassland sites under the same climate. In the subtropics (mediterranean climate with hot summers and mild winters), from both intensively cultivated arable land and grassland sites, N losses may exceed 200 kg^* ha^–1 year^–1. Without the use of irrigation the denitrification flux is negligible in spite of the high temperatures in this climate.     

Application of membrane inlet mass spectrometry to directly quantify denitrification in flooded rice paddy soil

Denitrification has long been considered a major mechanism of N loss when N fertilizer is applied to flooded rice paddies. However, the direct determination of denitrification in soils is almost impossible because of the high atmospheric background of dinitrogen (N₂). Dissolved N₂ in a small water sample can be rapidly and precisely measured through membrane inlet mass spectrometry (MIMS). This study is the first to directly measure N₂ flux through MIMS in flooded rice paddy plots that received different amounts of urea. Ammonia (NH₃) volatilization was measured simultaneously to verify whether NH₃ volatilization and denitrification are complementary loss mechanisms. The average cumulative N₂–N loss measured by MIMS 21 days after fertilization was 4.7?±?1.7 % of the applied N, which was within the range of the reported values obtained by cumulative recovery of (N₂ + N₂O)–¹⁵N and ¹⁵N-balance technique. Underestimation or overestimation of denitrification can be prevented in MIMS given that N₂ can be measured directly without ¹⁵N-labeled fertilizer. A good positive correlation was found between the dissolved in situ N₂ concentrations of floodwater and the denitrification rates of intact soil cores. Urea incorporation reduced NH₃ volatilization unlike surface broadcasting. However, urea incorporation significantly increased cumulative N₂–N loss during the 21 days after fertilization. Correlation analysis showed that nitrate (NO₃ ^?–N) concentration in floodwater could be the primary restricting factor for soil denitrification in the experimental field. Results suggest that MIMS is a promising technique for the measurement of denitrification in a flooded rice paddy.     

尿素和KNO3对水稻土无机氮转化过程和产物的影响Ⅱ.N2O生成过程

采用15N技术标记尿素和KNO3,研究了淹水条件下黄泥土和红壤性水稻土生成N2 O的主要过程。结果表明 ,黄泥土反硝化过程产物以N2 为主 ,N2 O的生成量可以略而不计。加入KNO3促进NO- 3异化还原成铵过程 ,从而增加N2 O生成速率。红壤性水稻土主要通过反硝化或好气反硝化过程生成N2 O ,随着土壤pH的提高或NO- 3 浓度升高 ,N2 O生成速率增大。无论是黄泥土还是红壤性水稻土 ,有相当一部分样本的N2 O的15N丰度在NO- 2 、NO- 3 、NH 4的15N丰度范围外 ,由此推论 ,氮转化生成N2 O的过程应在微生物细胞内进行。     

Assessing the potential of ammonia oxidizing bacteria to produce nitrous oxide in soils of a high arctic lowland ecosystem on Devon Island, Canada

The contribution of nitrifiers (ammonia-oxidizing bacteria (AOB)) and denitrifiers to nitrous oxide (N₂O) emission from arctic soils remains inconclusive. Based on preliminary experiments, we hypothesized that AOB are the primary producers of N₂O in a high arctic lowland ecosystem on Devon Island, Nunavut, Canada. In part 1 of the study, flux chambers were installed in a catena to determine in situ fluxes of gases (N₂O and carbon dioxide (CO₂)) from 16 June to 13 July 2004. Although fluxes were low, N₂O production occurred in the wettest area of the landscape when ammonium levels were high. As ammonium, but not nitrate, levels declined in the wet sedge meadow, N₂O emissions correspondingly decreased. In part 2, the contribution of nitrification and denitrification to N₂O production was assessed by Acetylene Inhibition Assay and ¹⁵N isotopically enriched incubations. Ammonium fertilization stimulated N₂O emissions to a greater extent than nitrate, and acetylene had a greater impact on N₂O emissions in ammonium-fertilized soils than in nitrate-amended soils. Stable isotope analysis indicated that at 50-55% water filled pore space, nitrification was the dominant (>80%) N₂O emitting process. In part 3, molecular analyses of the two N₂O producing groups indicated the both nitrifiers and denitrifiers did not differ between landforms. Our results suggest nitrifier denitrification is the dominant process occurring in these arctic soils and that the role of denitrifiers in N₂O release from arctic soils needs to be re-evaluated.     

Nitrogen and oxygen isotope ratios of nitrous oxide emitted from soil and produced by nitrifying and denitrifying bacteria

The isotopic composition at natural abundance levels of nitrous oxide emitted from a sandy loam, neutral pH soil under a range of soil water contents (matric potentials of-0.1,-1.0 and-5.0 kPa), from soil amended with sodium succinate and sodium ethanoate, and produced by pure cultures of the nitrifying bacteria Nitrosomonas europaea and Nitrosolobus multiformis, and by the denitrifying bacterium Pseudomonas putida, has been determined in laboratory experiments. N₂O from all sources was depleted in the ¹⁵N and ¹⁸O isotopes relative to the conventional references [atmospheric N₂ and standard mean ocean water (SMOW), respectively]. N₂O from soil was depleted in ¹⁵N and ¹⁸O to increasing extents with increasing soil water content. The isotopic composition of N₂O produced by N. europaea and N. multiformis was similar to that emitted from drier soil (matric potential of-1.0 kPa) and the N₂O produced by P. putida was similar to that emitted from wetter soil (matric potential of-0.1 kPa). N₂O emitted from the wetter soil was enriched in ¹⁵N and ¹⁸O compared with that emitted from the drier soil. The differences in isotopic composition between N₂O from the wetter and drier soil were attributed principally to isotopic fractionation during N₂O reduction to N₂ in the terminal step of denitrification. The effect of both sodium succinate and sodium ethanoate amendment was to increase the overall rate of N₂O emission, much of which arose from denitrification, as revealed by incubation in 100 kPa O₂. In addition, in the sodium ethanoate amended soil N₂O reduction to N₂ did not occur, as revealed by incubation in 10 kPa C₂H₂. The N₂O from the sodium ethanoate amended soil was depleted in ¹⁵N to a greater extent than the sodium succinate amended soil, which is consistent with the observation that N₂O reduction to N₂ leaves residual N₂O relatively enriched in ¹⁵N.     

一种直接测定硝化—反硝化气体的15N示踪—质谱法

本文对¹⁵N示踪—质谱法的可靠性进行了检验。结果表明,在不同的¹⁵N丰度气体样品的测定中,用两种方法(反硝化作用源的¹⁵N丰度法和气样的¹⁵N丰度法)计得的反硝化损失量基本一致,故建立起来的¹⁵N示踪—质谱法是可靠的。该方法的测定偏差随气样¹⁵N丰度的降低而增大。此外,回收率结果表明,(N₂+N₂O+NO_x)-¹⁵N累积释放量占加入NO₃-¹⁵N量的94.1％。因此,这一方法可用于直接测定氮肥的硝化—反硝化损失的研究中。     

Denitrification- and Nitrate Leaching-Losses in an Intensively Cropped Watershed

In continuation of former measurements about gaseous denitrification losses, these losses together with those by nitrate leaching were measured by different methods in a field cropped during two years by wheat. Furthermore, N-uptake by the plants of fertilizer- and soil-N as well as N-im-mobilization in soils during and after the cropping periods was determined by application of highly enriched¹⁵N-labeled fertilizer. Denitrification losses determined by the N₂O release from C₂H₂–treated undisturbed soil cores agreed reasonably well with losses obtained by ¹⁵N-balance measurements. They both amounted during the cropping periods 12–15 and 6–20 kg N ha^?1, respectively. Gaseous N-losses increased mainly during wet periods when the field was barren. Denitrifying enzyme activities and soil respiration (CO₂-release) was measured throughout one year. Leaching losses of NO₃ from soil-and fertilizer-N occurred only during fall until spring. Leached NO₃^? originated mostly from mineralized soil-N and very little from previously immobilized fertilizer-N.     

Nitrification activity in submerged soils and its relation to denitrification loss

Summary Nitrification activity (formation of NO ₂ ^– + NO ₃ ^– per unit soil weight) was measured in the surface layer of 15 presubmerged soils incubated in petri dishes under flooded but aerobic conditions. soils with pH above 5 nitrified quickly, whereas soils with pH below this level did not nitrify or nitrified slowly. The pH values between 7 and 8.5 were optimal for nitrification. Organic-matter levels in the 15 soils of our study did not influence their nitrification activities. In a follow-up greenhouse pot study, after a period of 3 weeks, ¹⁵N-balance measurements showed that the loss of N through apparent denitrification did not follow the nitrification patterns of the soils observed in the petri dishes. Apparent denitrification accounted for 16.8% and 18.9% loss of ¹⁵N from a soil with insignificant nitrification activity and a soil with high nitrification activity, respectively. These results, thus, indicate a lack of correspondence between the nitrification activities of soil and the denitrification loss of N when the former was measured in the dark and the latter was estimated in the light. Soils that nitrified in the darkness of the incubator did not nitrify in the daylight in the greenhouse.     

Gaseous nitrogen losses from fertilized soil during nitrification and denitrification using the acetylene blockage technique

Summary A sandy soil amended with different forms and amounts of fertilizer nitrogen (urea, ammonium sulphate and potassium nitrate) was investigated in model experiments for N₂O emission, which may be evolved during both oxidation of ammonia to nitrate and anaerobic respiration of nitrate. Since C₂H₂ inhibits both nitrification and the reduction of N₂O to N₂ during denitrification, the amount of N₂O evolved in the presence and absence of C₂H₂ represents the nitrogen released through nitrification and denitrification.Results show that amounts of N₂O-N lost from soils incubated anaerobically with 0.1% C₂H₂ and treated with potassium nitrate (23.1 µg N-NO ₃ ^– /g dry soil) exceeded those from soils incubated in the presence of 20% oxygen and treated with even larger amounts of nitrogen as urea and ammonium sulphate. This indicates that nitrogen losses by denitrification may potentially be higher than those occurring through nitrification.     

Nitrous oxide production by nitrification and denitrification in soil aggregates as affected by O2 concentration

Nitrous oxide emitted by soils can be produced either by denitrification in anoxic conditions or by nitrification in presence of O₂. The relative importance of the two processes, particularly under varied partial pressures of O₂, is not always known. This paper focuses on the influence of O₂ concentration on N₂O production by nitrification and denitrification in an arable Orthic Luvisol. Soil aggregates (2-3 mm size), water unsaturated, received 116 mg N kg⁻¹ as ammonium sulphate labelled with ¹⁵N and were incubated during 14 days at different O₂ partial pressures: 0, 0.35, 0.76, 1.5, 4.3 and 20.4 kPa. A ¹⁵N tracing technique was used to quantify nitrification and denitrification rates. ¹⁵N₂O and ¹⁵N₂ were measured. Oxygen pressure appeared to strongly influence both nitrification and denitrification rates and also N₂O emissions. Nitrification rates were reduced by a factor of 6-9 when O₂ decreased from 20.4 to 0.35 kPa. They were highly correlated with O₂ consumption rates. Denitrification mainly occurred in complete anoxic conditions. The proportion of N₂O emitted by denitrification was estimated by two independent methods: one based on ¹⁵N tracing using isotope composition of NH₄, NO₃ and N₂O, the other based on the measurement of the ¹⁵N₂O:¹⁵N₂ ratio. The two methods gave close results. The highest N₂O emissions were obtained under complete anoxic conditions and were due to denitrification. However, N₂O emissions almost as important were obtained at day 14 with 1.5 kPa O₂ pressure, and they were due to nitrification. Nitrification was the main source of N₂O at O₂ concentrations greater than 0.35 kPa. The amounts of N₂O-N emitted by nitrification were linearly related to the amounts of N nitrified, but the slope of the regression was highly dependent on O₂ concentration: it varied from 0.16 to 1.48% when O₂ concentration was reduced from 20.4 to 0.76 kPa. Emissions of N₂O by nitrification may then be quite significant if nitrification occurs at a reduced O₂ concentration.     

Evaluation of nitrate and ammonium as sources of NO and N2O emissions from black earth soils (Haplic Chernozem) based on 15N field experiments

Nitrous oxide (N₂O) and nitric oxide (NO) released from soil is a concern since it can act as a potential atmospheric pollutant and it represents a loss of N from the soil. These gases are present in the atmosphere in trace amounts and are important to atmospheric chemistry and earth's radiative balance. Nitric oxide (NO) does not directly contribute to the greenhouse effect, but it contributes to climate forcing through its role in photochemistry of hydroxyl radicals and ozone and plays a key role in air quality issues. Nitrification and denitrification have been identified as major controlling microbial processes in soils responsible for the formation of NO and N₂O. To elucidate the contribution of both processes to the release of NO and N₂O from loess-black earth soils under field conditions—i.e. to evaluate nitrate and ammonium as sources of NO and N₂O emission—two field experiments with either [¹⁵N] nitrate (NO₃^?) or [¹⁵N] ammonium (NH₄⁺) labelling have been conducted at two sites differing in soil organic matter content (high and normal SOM). [¹⁵N] nitrate treatments revealed that denitrification of NO₃^? represents the main pathway of soil N₂O release. On average 76% and 54% of N₂O was emitted during denitrification from soils with high and normal SOM content, respectively. Contrarily, denitrification contributed on average only 17% and 12% of released NO from soil with high and normal SOM content, respectively. The [¹⁵N]ammonium treatments revealed that nitrification of NH₄⁺ is the major process responsible for soil NO emission. SOM content of the loess-black earth soil significantly influenced NO and N₂O emission. The soil with the higher SOM content showed lower NO emission but drastically increased N₂O emission after nitrate fertilisation. In particular the soil with high SOM content exhibited a high sorption capacity for ammonium ions which led to unexpected results after fertilisation with [¹⁵N]ammonium. To explain this results a revised concept containing three different interacting soil ammonium pools have been hypothesised.