Effects of phosphorus addition on N2O and NO emissions from soils of an Acacia mangium plantation

Abstract

An incubation experiment was conducted to examine the effects of the phosphorus (P) application on nitrous oxide (N₂O) and nitric oxide (NO) emissions from soils of an Acacia mangium plantation in Indonesia. The soils were incubated with and without the addition of P (Ca[H₂PO₄]₂; 2 mg P g soil)^?1) after adjusting the water-filled pore space (WFPS) to 75% or 100%. The P addition increased N₂O emissions under both WFPS conditions and NO emissions at 75% WFPS. Some possible mechanisms are considered. First, the P addition stimulated nitrogen (N) cycling, and N used for nitrification and/or denitrification also increased. Second, the P addition could have relieved the P shortage for nitrifying and/or denitrifying bacteria, producing N₂O and NO. Our results suggest that the application of P fertilizer has the potential to stimulate N₂O and NO emissions from Acacia mangium plantations, at least when soils are under relatively wet conditions.     

Emissions of N2O from soils during cycles of freezing and thawing and the effects of soil water, texture and duration of freezing

Freezing and thawing influence many physical, chemical and biological processes in soils, including the production of trace gases. We studied the effects of freezing and thawing on three soils, one sandy, one silty and one loamy, on the emissions of N₂O and CO₂. We also studied the effect of varying the water content, expressed as the percentage of the water‐filled pore space (WFPS). Emissions of N₂O during thawing decreased in the order 64% > 55% > 42% WFPS, which suggests that the retardation of the denitrification was more pronounced than the acceleration of the nitrification with increasing oxygen concentration in the soil. However, emissions of N₂O at 76% WFPS were less than at 55% WFPS, which might be caused by an increased ratio of N₂/N₂O in the very moist conditions. The emission of CO₂ was related to the soil water, with the smallest emissions at 76% WFPS and largest at 42% WFPS. The emissions of CO₂ during thawing exceeded the initial CO₂ emissions before the soils were frozen, which suggests that the supply of nutrients was increased by freezing. Differences in soil texture had no marked effect on the N₂O emissions during thawing. The duration of freezing, however, did affect the emissions from all three soils. Freezing the soil for less than 1 day had negligible effects, but freezing for longer caused concomitant increases in emissions. Evidently the duration of freezing and soil water content have important effects on the emission of N₂O, whereas the effects of texture in the range we studied were small.     

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.     

N2O, NO, and NH3 Emissions from Soil after the Application of Organic Fertilizers, Urea and Water

Agricultural soil is a major source of nitrous oxide (N₂O), nitric oxide (NO) and ammonia (NH₃). Little information is available on emissions of these gases from soils amended with organic fertilizers at different soil water contents. N₂O, NO and NH₃ emissions were measured in large-scale incubations of a fresh sandy loam soil and amended with four organic fertilizers, [poultry litter (PL), composted plant residues (CP), sewage sludge pellets (SP) and cattle farm yard manure (CM)], urea fertilizer (UA) or a zero-N control (ZR) for 38 days. Fertilizers were added to soil at 40, 60 or 80% water-filled pore space (WFPS). The results showed that urea and organic fertilizer were important sources of N₂O and NO. Total N₂O and NO emissions from UA ranged from 0.04 to 0.62%, and 0.23 to 1.55% of applied N, respectively. Total N₂O and NO emissions from organic fertilizer treatments ranged from 0.01 to 1.65%, and <0.01 to=" 0.55%=" of=" applied=" n,=" respectively.=" the=" lower=">₂O and NO emissions from CP and CM suggested that applying N is these forms could be a useful mitigation option. Comparison of the NO-N/N₂O-N ratio suggested that nitrification was more dominant in UA whereas denitrification was more dominant in the organic fertilizer treatments. Most N was lost from PL and UA as NH₃, and this was not influenced significantly by WFPS. Emissions of NH₃ from UA and PL ranged from 62.4 to 69.6%, and 3.17 to 6.11% of applied N, respectively.     

The influence of soluble carbon and fertilizer nitrogen on nitric oxide and nitrous oxide emissions from two contrasting agricultural soils

Contradictory effects of simultaneous available organic C and N sources on nitrous oxide (N₂O), carbon dioxide (CO₂) and nitric oxide (NO) fluxes are reported in the literature. In order to clarify this controversy, laboratory experiments were conduced on two different soils, a semiarid arable soil from Spain (soil I, pH=7.5, 0.8%C) and a grassland soil from Scotland (soil II, pH=5.5, 4.1%C). Soils were incubated at two different moisture contents, at a water filled pore space (WFPS) of 90% and 40%. Ammonium sulphate, added at rates equivalent to 200 and 50 kg N ha^?1, stimulated N₂O and NO emissions in both soils. Under wet conditions (90% WFPS), at high and low rates of N additions, cumulative N₂O emissions increased by 250.7 and 8.1 ng N₂O–N g^?1 in comparison to the control, respectively, in soil I and by 472.2 and 2.1 ng N₂O–N g^?1, respectively, in soil II. NO emissions only significantly increased in soil I at the high N application rate with and without glucose addition and at both 40% and 90% WFPS. In both soils additions of glucose together with the high N application rate (200 kg N ha^?1) reduced cumulative N₂O and NO emissions by 94% and 55% in soil I, and by 46% and 66% in soil II, respectively. These differences can be explained by differences in soil properties, including pH, soil mineral N and total and dissolved organic carbon content. It is speculated that nitrifier denitrification was the main source of NO and N₂O in the C-poor Spanish soil, and coupled nitrification–denitrification in the C-rich Scottish soil.     

Time-lagged induction of N2O emission and its trade-off with NO emission from a nitrogen fertilized Andisol

Abstract

To understand the influence of basal application of N fertilizer on nitrification potential and N₂O and NO emissions, four soil samples were collected from an upland Andisol field just before (sample 1) and 4 (sample 2), 36 (sample 3) and 72 (sample 4) days after the basal application of N fertilizer during the Chinese cabbage growing season from 12 September to 30 November 2005. The potentials of N₂O production and nitrification of the soils were determined using a ¹⁵N tracer technique and the soils were incubated for 25 days at 25°C and 60% water-filled pore space (WFPS). The results revealed that as much as 84–97% N₂O and almost all NO were produced by nitrification. The ¹⁵N₂O emission peak occurred approximately 350 h after the beginning of incubation for samples 1 and 2, but just 48 h later in samples 3 and 4. Total ¹⁵N₂O emission during the 25-day incubation of samples 3 and 4 ranged from 190 to 198 µg N kg^?1 soil, which was significantly higher than the 99–108 µg N kg^?1 soil recorded in samples 1 and 2. Basal application of N fertilizer did not immediately increase the nitrification potential and the ratio of N₂O to N added, but did dramatically increase the nitrification potential and the ratio of N₂O to N added as (¹⁵NH₄)₂SO₄ 36–72 days after the basal N fertilizer was added. In contrast, NO emission was negatively correlated with nitrification potential and total N₂O emission. As a result, a trade-off relationship between total NO and N₂O emissions was identified. The results indicated that there was a time-lagged induction of the change of N turnover in the soil, which was possibly caused by slow population growth of the nitrifiers and/or a slow shift in the microbial community in the soil.     

Nitrous oxide emissions from animal urine application on a New Zealand pasture

Animal excreta-nitrogen (N) deposited onto pastoral soils during grazing has been identified as an important source of nitrous oxide (N₂O). Understanding the extent and seasonal variation of N₂O emissions from animal urine is important for the development of best management practices for reducing N₂O losses. The aim of this study was to determine N₂O emissions from cow urine after application onto a pastoral soil in different seasons between 2003 and 2005. A closed soil chamber technique was used to measure the N₂O emissions from a poorly drained silt loam soil which received either 0 (control) or 1,000 kg N ha⁻¹ (as real cow urine) per application. Application of cow urine to soil increased N₂O fluxes above those from the control site for up to 6 weeks, but the duration for which N₂O levels were elevated depended on the season. Nitrous oxide emissions were higher during the winter and spring measurement periods when the soil water-filled pore space (WFPS) was mostly above field capacity, and the emissions were lower during the summer and autumn measurement periods when the soil WFPS was below field capacity. The N₂O emission factor for urine ranged from 0.02 to 1.52% of N applied. This seasonal effect suggests that a reduction in urine return to soil (e.g., through use of standoff pads or animal housing) under wet conditions in New Zealand can potentially reduce N₂O emissions from pastoral soils.     

Laboratory investigations into the effects of the pesticides mancozeb, chlorothalonil, and prosulfuron on nitrous oxide and nitric oxide production in fertilized soil

Independent soil microcosm experiments were used to investigate the effects of the fungicides mancozeb and chlorothalonil, and the herbicide prosulfuron, on N₂O and NO production by nitrifying and denitrifying bacteria in fertilized soil. Soil cores were amended with NH₄NO₃ or NH₄NO₃ and pesticide, and the N₂O and NO concentrations were monitored periodically for approximately 48 h following amendment. Nitrification is the major source of N₂O and NO in these soils at soil moistures relevant to those observed at the field site where the cores were collected. At pesticide concentrations from 0.02 to 10 times that of a standard single application on a corn crop, N₂O and NO production was inhibited by all three pesticides. Generally N₂O production was inhibited by the pesticides from 10 to 62% and 20 to 98% at the lowest and highest dosages, respectively. Nitric oxide production was generally inhibited from about 5 to 47% and by 20 to 97% at the lowest and highest dosages, respectively. Nitrous oxide and nitric oxide production by nitrification was more susceptible to inhibition by these pesticides than denitrification. Production of both N₂O and NO by nitrification was inhibited by as much as 99%, at the highest concentration of pesticide applied. The net production of N₂O increased as soil moisture increased. The rate of NO production was greatest at the intermediate moistures investigated, between 14 and 19% gravimetric soil moisture, suggestive that nitrification is the dominant source of NO.     

Processes responsible for the nitrous oxide emission from a Costa Rican Andosol under a coffee agroforestry plantation

We used the inhibitor acetylene (C₂H₂) at partial pressures of 10 Pa and 10 kPa to inhibit autotrophic nitrification and the reduction of nitrous oxide (N₂O) to N₂, respectively. Soils (Andosol) from a Coffea arabica plantation shaded by Inga densiflora in Costa Rica were adjusted to 39, 58, 76 and 87% water-filled pore space (WFPS) and incubated for 6 days in the absence or presence of C₂H₂. Soil respiration, nitrification rates and N₂O emissions by both processes were measured in relation to soil moisture conditions. At all WFPS studied, rates of N₂O and N₂ productions were small (4.8; 14.7; 23 and 239.6 ng N–N₂O g⁻¹ d.w. d⁻¹ at 39, 58, 76 and 87% WFPS, respectively), and despite a low soil pH (4.7), N₂O was mainly produced by nitrification, which was responsible for 85, 91, 84 and 87% of the total N₂O emissions at 39, 58, 76 and 87% WFPS, respectively. At the three smaller values of WFPS, a linear relationship was established between WFPS, soil respiration, nitrification and N₂O released by nitrification; no N₂ was produced by denitrification. At more anaerobic conditions achieved by a WFPS of 87%, a large rate of N₂O production was measured during nitrification, and N₂ production accounted for 84% of the gaseous N fluxes caused by denitrification.     

土壤温度、水分和NH4+-N浓度对土壤硝化反应速度及N2O排放的影响

硝化反应是土壤、特别是干旱半干旱地区农业土壤N2O产生的重要途径之一。但是,目前环境条件对硝化反应中N2O排放的影响研究较少,而在国内外通用的几个模型中均用固定比例估算硝化反应过程中N2O的排放。本文通过砂壤土培养试验,研究了土壤温度、水分和NH4+-N浓度对硝化反应速度及硝化反应中N2O排放的影响,并用数学模型定量表示了各因素对硝化反应的作用,用最小二乘法最优拟合求得该土壤的最大硝化反应速度及N2O最大排放比例。结果表明,随着温度升高,硝化反应速度呈指数增长;水分含量由20%充水孔隙度(WFPS)增加到40%WFPS时,反应速度增加,水分含量增加到60%WFPS时反应速度略有降低;NH4+-N浓度增加对硝化反应速度起抑制作用。用米氏方程描述该土壤的硝化反应过程,其最大硝化反应速度为6.67mg·kg?1·d?1。硝化反应中N2O排放比例随温度升高而降低;随NH4+-N浓度增加而略有增加;20%和40%WFPS水分含量时,硝化反应中N2O排放比例为0.43%～1.50%,最小二乘法求得的最大比例为3.03%,60%WFPS时可能由于反硝化作用,N2O排放比例急剧增加,还需进一步研究水分对硝化反应中N2O排放的影响。     

Effects of nitrogen fertilization and irrigation on N2O emissions from a sandy soil in Germany

The aim of this study was to investigate the effect of supplemental irrigation on the amount of N₂O emissions on a sandy soil in north-east Germany. N₂O flux measurements were carried out over two vegetation periods from the emergence of plants to harvest. The level of N₂O emissions was low, which is typical for sandy soils in north-east Germany. In both periods, irrigation had no increasing effect on N₂O emissions. Relevant factors were the soil temperature and the soil water-filled pore space (WFPS), which were mainly influenced by weather conditions. This may indicate that nitrification was the main source of N₂O emissions. In conclusion, this study has confirmed that sandy soils under weather conditions of north-east Germany generally have a very low potential for N₂O emissions.     

Effects of soil moisture on gross N transformations and N2O emission in acid subtropical forest soils

Soil moisture changes, arising from seasonal variation or from global climate changes, could influence soil nitrogen (N) transformation rates and N availability in unfertilized subtropical forests. A ¹⁵?N dilution study was carried out to investigate the effects of soil moisture change (30–90 % water-holding capacity (WHC)) on potential gross N transformation rates and N₂O and NO emissions in two contrasting (broad-leaved vs. coniferous) subtropical forest soils. Gross N mineralization rates were more sensitive to soil moisture change than gross NH₄ ⁺ immobilization rates for both forest soils. Gross nitrification rates gradually increased with increasing soil moisture in both forest soils. Thus, enhanced N availability at higher soil moisture values was attributed to increasing gross N mineralization and nitrification rates over the immobilization rate. The natural N enrichment in humid subtropical forest soils may partially be due to fast N mineralization and nitrification under relatively higher soil moisture. In broad-leaved forest soil, the high N₂O and NO emissions occurred at 30 % WHC, while the reverse was true in coniferous forest soil. Therefore, we propose that there are different mechanisms regulating N₂O and NO emissions between broad-leaved and coniferous forest soils. In coniferous forest soil, nitrification may be the primary process responsible for N₂O and NO emissions, while in broad-leaved forest soil, N₂O and NO emissions may originate from the denitrification process.     

中国东北苹果园中土壤总硝化作用和氧化亚氮排放状况

A better understanding of nitrogen (N) transformation in agricultural soils is crucial for the development of sustainable and environmental-friendly N fertilizer management and the proposal of effective N₂O mitigation strategies. This study aimed: i) to elucidate the seasonal dynamic of gross nitrification rate and N2O emission, ii) to determine the influence of soil conditions on the gross nitrification, and iii) to confirm the relationship between gross nitrification and N₂O emissions in the soil of an apple orchard in Yantai, Northeast China. The gross nitrification rates and N₂O fluxes were examined from March to October in 2009, 2010, and 2011 using the barometric process separation (BaPS) technique and the static chamber method. During the wet seasons gross nitrification rates were 1.64 times higher than those under dry season conditions. Multiple regression analysis revealed that gross nitrification rates were significantly correlated with soil temperature and soil water-filled pore space (WFPS). The relationship between gross nitrification rates and soil WFPS followed an optimum curve peaking at 60% WFPS. Nitrous oxide fluxes varied widely from March to October and were stimulated by N fertilizer application. Statistically significant positive correlations were found between gross nitrification rates and soil N₂O emissions. Further evaluation indicated that gross nitrification contributed significantly to N₂O formation during the dry season (about 86%) but to a lesser degree during the wet season (about 51%). Therefore, gross nitrification is a key process for the formation of N₂O in soils of apple orchard ecosystems of the geographical region.     

Responses of soil nitrous oxide production and abundances and composition of associated microbial communities to nitrogen and water amendment

Soil moisture and nitrogen (N) are two important factors influencing N₂O emissions and the growth of microorganisms. Here, we carried out a microcosm experiment to evaluate effects of soil moisture level and N fertilizer type on N₂O emissions and abundances and composition of associated microbial communities in the two typical arable soils. The abundances and community composition of functional microbes involved in nitrification and denitrification were determined via quantitative PCR (qPCR) and terminal restriction length fragment polymorphism (T-RFLP), respectively. Results showed that N₂O production was higher at 90% water-filled pore (WFPS) than at 50% WFPS. The N₂O emissions in the two soils amended with ammonium were higher than those amended with nitrate, especially at relatively high moisture level. In both soils, increased soil moisture stimulated the growth of ammonia-oxidizing bacteria (AOB) and nitrite reducer (nirK). Ammonium fertilizer treatment increased the population size of AOB and nirK genes in the alluvial soil, while reduced the abundances of ammonia-oxidizing archaea (AOA) and denitrifiers (nirK and nosZ) in the red soil. Nitrate addition had a negative effect on AOA abundance in the red soil. Total N₂O emissions were positively correlated to AOB abundance, but not to other functional genes in the two soils. Changed soil moisture significantly affected AOA rather than AOB community composition in both soils. The way and extent of N fertilizers impacted on nitrifier and denitrifier community composition varied with N form and soil type. These results indicate that N₂O emissions and the succession of nitrifying and denitrifying communities are selectively affected by soil moisture and N fertilizer form in the two contrasting types of soil.     

Temperature responses of NO and N2O emissions from boreal organic soil

Both NO and N₂O are produced in soil microbial processes and have importance in atmospheric physics and chemistry. In recent years several studies have shown that N₂O emissions from organic soils can be high at low temperatures. However, the effects of low temperature on NO emissions from soil are unknown. We studied in laboratory conditions, using undisturbed soil cores, the emissions of NO and N₂O from organic soils at various temperatures, with an emphasis on processes and emissions during soil freezing and thawing periods. We found no soil freezing- or thawing-related emission maxima for NO, while the N₂O emissions were higher both during soil freezing and thawing periods. The results suggest that different factors are involved in the regulation of NO and N₂O emissions at low temperatures.     

Contributions of nitrification and denitrification to N2O emissions from soils at different water-filled pore space

A combination of stable isotope and acetylene (0.01% v/v) inhibition techniques were used for the first time to determine N₂O production during denitrification, autotrophic nitrification and heterotrophic nitrification in a fertilised (200 kg N ha^–1) silt loam soil at contrasting (20–70%) water-filled pore space (WFPS). ¹⁵N-N₂O emissions from ¹⁴NH₄¹⁵NO₃ replicates were attributed to denitrification and ¹⁵N-N₂O from ¹⁵NH₄¹⁵NO₃ minus that from ¹⁴NH₄¹⁵NO₃ replicates was attributed to nitrification and heterotrophic nitrification in the presence of acetylene, as there was no dissimilatory nitrate reduction to ammonium or immobilisation and remineralisation of ¹⁵N-NO₃^–. All of the N₂O emitted at 70% WFPS (31.6 mg N₂O-N m^–2 over 24 days; 1.12 g N₂O-N g dry soil^–1; 0.16% of N applied) was produced during denitrification, but at 35–60% WFPS nitrification was the main process producing N₂O, accounting for 81% of ¹⁵N-N₂O emitted at 60% WFPS, and 7.9 g ¹⁵N-N₂O m^–2 (0.28 ng ¹⁵N-N₂O g dry soil^–1) was estimated to be emitted over 7 days during heterotrophic nitrification in the 50% WFPS treatment and accounted for 20% of ¹⁵N-N₂O from this treatment. Denitrification was the predominant N₂O-producing process at 20% WFPS (2.6 g ¹⁵N-N₂O m^–2 over 7 days; 0.09 ng ¹⁵N-N₂O g dry soil^–1; 85% of ¹⁵N-N₂O from this treatment) and may have been due to the occurrence of aerobic denitrification at this WFPS. Our results demonstrate the usefulness of a combined stable isotope and acetylene approach to quantify N₂O emissions from different processes and to show that several processes may contribute to N₂O emission from agricultural soils depending on soil WFPS.     

Nitrogen oxides emission from soils bearing a potato crop as influenced by fertilization with treated pig slurries and composts

Nitrous oxide, nitric oxide and denitrification losses from an irrigated soil amended with organic fertilizers with different soluble organic carbon fractions and ammonium contents were studied in a field study covering the growing season of potato (Solanum tuberosum). Untreated pig slurry (IPS) with and without the nitrification inhibitor dicyandiamide (DCD), digested thin fraction of pig slurry (DTP), composted solid fraction of pig slurry (CP) and composted municipal solid waste (MSW) mixed with urea were applied at a rate of 175 kg available N ha⁻¹, and emissions were compared with those from urea (U) and a control treatment without any added N fertilizer (Control). The cumulative denitrification losses correlated significantly with the soluble carbohydrates, dissolved N and total C added. Added dissolved organic C (DOC) and dissolved N affected the N₂O/N₂ ratio, and a lower ratio was observed for organic fertilizers than from urea or unfertilized controls. The proportion of N₂O produced from nitrification was higher from urea than from organic fertilizers. Accumulated N₂O losses during the crop season ranged from 3.69 to 7.31 kg N₂O-N ha⁻¹ for control and urea, respectively, whereas NO losses ranged from 0.005 to 0.24 kg NO-N ha⁻¹, respectively. Digested thin fraction of pig slurry compared to IPS mitigated the total N₂O emission by 48% and the denitrification rate by 33%, but did not influence NO emissions. Composted pig slurry compared to untreated pig slurry increased the N₂O emission by 40% and NO emission by 55%, but reduced the denitrification losses (34%). DCD partially inhibited nitrification rates and reduced N₂O and NO emissions from pig slurry by at least 83% and 77%, respectively. MSW+U, with a C:N ratio higher than that of the composted pig slurry, produced the largest denitrification losses (33.3 kg N ha⁻¹), although N₂O and NO emissions were lower than for the U and CP treatments.This work has shown that for an irrigated clay loam soil additions of treated organic fertilizers can mitigate the emissions of the atmospheric pollutants NO and N₂O in comparison with urea.     

Contribution of nitrification and denitrification to N2O emissions from urine patches

Urine deposition by grazing livestock causes an immediate increase in nitrous oxide (N₂O) emissions, but the responsible mechanisms are not well understood. A nitrogen-15 (¹⁵N) labelling study was conducted in an organic grass-clover sward to examine the initial effect of urine on the rates and N₂O loss ratio of nitrification (i.e. moles of N₂O-N produced per moles of nitrate produced) and denitrification (i.e. moles of N₂O produced per moles of N₂O+N₂ produced). The effect of artificial urine (52.9 g N m⁻²) and ammonium solution (52.9 g N m⁻²) was examined in separate experiments at 45% and 35% water-filled pore space (WFPS), respectively, and in each experiment a water control was included. The N₂O loss derived from nitrification or denitrification was determined in the field immediately after application of ¹⁵N-labelled solutions. During the next 24 h, gross nitrification rates were measured in the field, whereas the denitrification rates were measured in soil cores in the laboratory. Compared with the water control, urine application increased the N₂O emission from 3.9 to 42.3 μg N₂O-N m⁻² h⁻¹, whereas application of ammonium increased the emission from 0.9 to 6.1 μg N₂O-N m⁻² h⁻¹. In the urine-affected soil, nitrification and denitrification contributed equally to the N₂O emission, and the increased N₂O loss resulted from a combination of higher rates and higher N₂O loss ratios of the processes. In the present study, an enhanced nitrification rate seemed to be the most important factor explaining the high initial N₂O emission from urine patches deposited on well-aerated soils.     

Isotopomer signatures of soil-emitted N2O under different moisture conditions—A microcosm study with arable loess soil

Soils represent the major source of the atmospheric greenhouse gas nitrous oxide (N₂O) and there is a need to better constrain the total global flux and the relative contribution of the microbial source processes. The aim of our study was to evaluate isotopomer analysis of N₂O (intramolecular distribution of ¹⁵N) as well as conventional nitrogen and oxygen isotope ratios (i) as a tool to identify N₂O production processes in soils and (ii) to constrain the isotopic fingerprint of soil-derived N₂O. We conducted a microcosm study with arable loess soil fertilized with 20 mg N kg⁻¹ of ¹⁵NO₃⁻-labeled or non-labeled ammonium nitrate. Soils were incubated for 16 d at varying moisture (55%, 75% and 85% water-filled pore space (WFPS)) in order to establish different levels of nitrification and denitrification. Dual isotope and isotopomer ratios of emitted N₂O were determined by mass spectrometric analysis of δ¹⁸O, average δ¹⁵N (δ¹⁵N^bulk) and ¹⁵N site preference (SP=difference in δ¹⁵N between the central and peripheral N-positions of the asymmetric N₂O molecule). Total rates and N₂O emission of denitrification and nitrification were determined by ¹⁵N analysis of headspace gases and soil extracts of the ¹⁵NO₃⁻ treatment. N₂O emission and denitrification increased with moisture whereas gross nitrification was almost constant. In the 55% WFPS treatment, more than half of the N₂O flux was derived from nitrification, whereas denitrification was the dominant N₂O source in the 75% WFPS and 85% WFPS treatments. Moisture conditions were reflected by the isotopic signatures since highly significant differences were observed for average δ¹⁵N^bulk, SP and δ¹⁸O. Experiment means of the 75% WFPS and 85% WFPS treatments gave negative δ¹⁵N^bulk (−18.0‰ and −34.8‰, respectively) and positive SP (8.6‰ and 15.3‰, respectively), which we explained by the fractionation during N₂O production and partial reduction to N₂. In the 55% WFPS treatment, mean SP was relatively low (1.9‰), which suggests that nitrification produced N₂O with low or negative SP. The observed influence of process condition on isotopomer signatures suggests that the isotopomer approach might be suitable for identifying N₂O source processes. However, more research is needed to determine the impact from process rates and microbial community structure. Isotopomer signatures were within the range reported from previous soil studies which supports the assumption that SP of soil-derived N₂O is lower than SP of tropospheric N₂O.     

Efficiency of nitrification inhibitor DMPP to reduce nitrous oxide emissions under different temperature and moisture conditions

Agricultural intensification has led to the use of very high inputs of nitrogen fertilizers into cultivated land. As a consequence of this, nitrous oxide (N₂O) emissions have increased significantly. Nowadays, the challenge is to mitigate these emissions in order to reduce global warming. Addition of nitrification inhibitors (NI) to fertilizers can reduce the losses of N₂O to the atmosphere, but field studies have shown that their efficiency varies depending greatly on the environmental conditions. Soil water content and temperature are key factors controlling N₂O emissions from soils and they seem to be also key parameters responsible for the variation in nitrification inhibitors efficiency. We present a laboratory study aimed at evaluating the effectiveness of the nitrification inhibitor 3,4-dimethylpyrazol phosphate (DMPP) at three different temperatures (10, 15 and 20 °C) and three soil water contents (40%, 60% and 80% of WFPS) on N₂O emissions following the application of 1.2 mg N kg⁻¹ dry soil (equivalent to 140 kg N ha⁻¹). Also the CO₂ and CH₄ emissions were followed to see the possible side effects of DMPP on the overall microbial activities. Nitrogen was applied either as ammonium sulfate nitrate (ASN) or as ENTEC 26 (ASN + DMPP). The application of ENTEC 26 was effective reducing N₂O losses up to the levels of an unfertilized control treatment in all conditions. Nevertheless, the percentage of reduction induced by DMPP in the ENTEC treatment with respect to the ASN varied from 3% to 45% depending on temperature and soil water content conditions. At 40% of WFPS, when nitrification is expected to be the main process producing N₂O, the increase of N₂O emissions in ASN together with temperature provoked an increase in DMPP efficiency reducing these emissions from 17% up to 42%. Contrarily, at 80% of WFPS, when denitrification is expected to be the main source of N₂O, emissions after ASN application decreased with temperature, which induced a decrease from 45% to 23% in the efficiency of DMPP reducing N₂O losses. Overall, the results obtained in this study suggest that DMPP performance regarding N₂O emissions reduction would be the best in cold and wet conditions. Neither CO₂ emissions nor CH₄ emissions were affected by the use of DMPP at the different soil water contents and temperatures.