Nitrous oxide emission from urine-treated soil as influenced by urine composition and soil physical conditions

Urine patches from cattle and sheep on pastures represent considerable, highly localized N applications. Subsequent nitrification and denitrification of the nitrogenous compounds may result in high nitrous oxide (N₂O) emissions. Not much is known about the extent of these emissions, or about possible mitigation options. The aims of this study were to experimentally quantify the effects of urine composition, dung addition, compaction and soil moisture on N₂O emissions from urine patches. For an incubation study at 16 °C, soil was collected from a typic Endoaquoll, and N₂O production was monitored during a 103-day period. Emissions for the whole period averaged 0.3 and 0.9% of the applied urine-N for dry and moist soil, respectively. When compacted or when dung was added, emissions from moist soils increased to 4.9 and 7.9%, respectively. Both addition of dung and soil compaction resulted in a delay of the peak N₂O emission of approximately 10-15 days. No significant effect of amount of urine-N on emission percentages was detected. Changing the volume of urine with equal amounts of urine-N resulted in highly significant effects, peaking with an emission of 2.3% at a water-filled pore space (WFPS) of 78%. When the soil was water-saturated, N₂O production was delayed until evaporation had decreased moisture contents. We concluded that denitrification was the main N₂O forming process in the incubation study. Emission factors for urine reported in the literature do not generally include the potentially considerable effects of compaction or combination with dung. We conclude that realistic emission factors should take into account such an effect, together with estimates for the occurrence of camping areas in pastures. From our results, the best mitigation strategies appear to be increasing the volume of urine through feed additives, and avoiding compaction and promoting more homogeneous application of N through a lower cattle stocking rate. Also, research efforts may be targeted at management practices to avoid camping areas in pastures.     

Nitrous oxide emission from frozen grassland soil and during thawing periods

Nitrous oxide (N₂O) was emitted during a frost period from an old grassland as well as during thawing. Soil incubations at various times throughout the freezing period showed that highest emission rates were emitted around 0 °C, and the magnitude of the emission peak increased with the length of the freezing period. Highest N₂O emissions during freezing and thawing were measured from soil previously treated with nitrate (NO₃^‐). The emitted N₂O was produced via reduction of NO₃^‐. The steady drop in N₂O emission at soil temperatures higher than 2 °C coincided with large dinitrogen (N₂) emissions which most likely reflected the increasing enzymatic activity of N₂O reductase with increasing temperatures. Measurements of mineral N concentrations showed that NO₃^‐ and NH₄⁺, which were shortly after fertilizer application immobilized into the microbial biomass, became partly available again through the freezing effect and caused large N₂O emissions in winter. This study provided evidence that N₂O emissions during freezing and thawing in the winter are due to biological rather than chemical activity in soil.     

Nitrous oxide emission from herbicide-treated soybean

 The emission of N₂O from soybean plants treated with the herbicides dichlorophenoxyacetic acid (2,4-D) and bromoxynil was studied. The N₂O flux from 2,4-D- and bromoxynil-treated soybean was 14.1 ng N₂O-N g^–1 fresh weight h^–1 and 19.7 ng N₂O-N g^–1 fresh weight h^–1, respectively, i.e. approximately twice that of the controls. The NO₂ ^–-N concentration in 2,4-D- and in bromoxynil-treated soybean was about 8 μg N g^–1 fresh weight, i.e. fivefold the concentration found in control plants. The NO₃ ^– content in herbicide-treated soybean did not differ significantly from that of the control plants. Consequently, the accumulation of NO₂ ^–-N during the assimilation of NO₃ ^–-N was thought to cause the observed N₂O release. Probably, N₂O is a by-product produced during either the reaction of NO₂ ^–-N with plant metabolites or NO₂ ^–-N decomposition. Final conclusions must await further experiments. Received: 5 November 1999     

Nitrous oxide emission from animal manures applied to soil under controlled conditions

Animal manures may differ strongly in composition and as a result may differ in the emission of N₂O following application to soil. An incubation study was carried out to assess the effects of type of mineral N fertilizer and manure, application technique and application rate on N₂O emission from a sandy soil with low organic matter content. Fluxes of N₂O were measured 30 times over a 98-day period. The total N₂O emission from mineral N fertilizer ranged from 2.1 to 4.0% of the N applied. High emissions were associated with manures with high contents of inorganic N, easily mineralizable N and easily mineralizable C, such as liquid pig manure (7.3-13.9% of the N applied). The emission from cattle slurries ranged from 1.8 to 3.0% and that of poultry manures from 0.5 to 1.9%. The total N₂O emission during the experimental period tended to increase linearly with increasing N application rate of NH₄NO₃ and liquid pig manure. The N₂O emission from surface-applied NH₄NO₃ was significantly smaller than that following the incorporation of NH₄NO₃ in the soil. The N₂O emission from pig manure placed in a row at 5 cm depth was significantly higher than from surface-application and other techniques in which manure was incorporated in the soil. The results show that modification of the composition and application technique may be tools to mitigate emission of N₂O.     

Nitrous oxide emission from a grassland soil fertilized with slurry and calcium nitrate

Concentrations of nitrous oxide (N₂O) and oxygen were monitored over a 2-yr period in an imperfectly drained grassland soil receiving applications of N as cattle slurry or Ca(NO₃)₂. In both years N₂O concentrations in the different treatments were in the order nitrate > slurry > control. Gaseous diffusion coefficients were determined in soil cores by a krypton-85 tracer method and used to calculate approximate N₂O fluxes from the soil. Only 1–5 kg N ha^?1 was lost as N₂O after a single application of > 1200 kg N ha ^?1 as slurry compared with 3–11 kg N ha ^?1 lost after 100 kg was added as NO₃^?. Total gaseous losses (N₂O+N₂) could be expected to be higher in both cases.     

Nitrous oxide emission from wetland rice soil as affected by the application of controlled-availability fertilizers and mid-season aeration

 N₂O emission from a wetland rice soil as affected by the application of three controlled-availability fertilizers (CAFs) and urea was investigated through a pot experiment. N₂O fluxes from the N fertilized paddy soil averaged 44.8–69.3 μg N m^–2 h^–1 during the rice growing season, accounting for 0.28–0.51% of the applied N. The emission primarily occurred during the mid-season aeration (MSA) and the subsequent re-flooding period. Fluxes were highly correlated with the NO₃ ^– and N₂O concentrations in the soil water. As there were relatively large amounts of NH₄ ⁺-N present in the soil of the CAF treatments at the beginning of MSA, leading to large amounts of NO₃ ^–-N during the MSA and the subsequent re-flooding period, the tested CAFs were not effective in reducing N₂O emission from this paddy soil. The potential of applied CAFs to reduce N₂O emissions from paddy soil is discussed. Received: 25 May 1999     

Nitrous oxide emission as affected by changes in soil water content and nitrogen fertilization

Nitrous oxide emission was measured in laboratory incubations of an alluvial soil (58% clay, pH 7.4). The soil was amended with 40 mg N kg⁻¹ as NaNO₃ or NH₄Cl, or with NaCl as a control. Each fertilization treatment was adjusted to three different water contents: constant 60% WHC (water-holding capacity), constant 120% WHC, and water content alternating between 60 and 120% WHC. During an 8-day incubation period N₂O emission rates and inorganic nitrogen concentrations in soil (NH₄⁺, NO₂⁻, NO₃⁻) were determined at regular intervals. In the control and after nitrate application small N₂O emission rates occurred with only minor variations over time, and no differences between the water treatments. In contrast, with ammonium application N₂O emission rates were much higher during the first two days of incubation, with peaks in the constant 60% WHC and 120% WHC at day 1 and in the changing-water treatment at day 2, when the first wet period (120% WHC) was completed. This N₂O peak in the changing-water treatment was 4 to 9 times higher than with constant WHC and occurred when both, NH₄⁺ and NO₂⁻ concentrations declined sharply. Thus, this N₂O emission flush can be attributed to nitrifier denitrification. After the second rewetting of the NH₄⁺-amended soil no further N₂O emission peak was observed, being in accordance with small NH₄⁺ and NO₂⁻ concentrations in soil at that time. The unexpectedly small N₂O fluxes in the constant 120% WHC treatment after nitrate application were probably caused by the reduction of N₂O to N₂ under the prevailing conditions. It can be concluded that continuous wetting or flooding of a soil is an effective measure to reduce N₂O emissions immediately after the application of NH₄⁺ fertilizers.     

Nitrous oxide emission derived from soil organic matter decomposition from tropical agricultural peat soil in central Kalimantan,Indonesia

Our previous research showed large amounts of nitrous oxide (N₂O) emission (>200?kg?N?ha^?1?year^?1) from agricultural peat soil. In this study, we investigated the factors influencing relatively large N₂O fluxes and the source of nitrogen (N) substrate for N₂O in a tropical peatland in central Kalimantan, Indonesia. Using a static chamber method, N₂O and carbon dioxide (CO₂) fluxes were measured in three conventionally cultivated croplands (conventional), an unplanted and unfertilized bare treatment (bare) in each cropland, and unfertilized grassland over a three-year period. Based on the difference in N₂O emission from two treatments, contribution of the N source for N₂O was calculated. Nitrous oxide concentrations at five depths (5–80?cm) were also measured for calculating net N₂O production in soil. Annual N fertilizer application rates in the croplands ranged from 472 to 1607?kg?N?ha^?1?year^?1. There were no significant differences in between N₂O fluxes in the two treatments at each site. Annual N₂O emission in conventional and bare treatments varied from 10.9 to 698 and 6.55 to 858?kg?N?ha^?1?year^?1, respectively. However, there was also no significant difference between annual N₂O emissions in the two treatments at each site. This suggests most of the emitted N₂O was derived from the decomposition of peat. There were significant positive correlations between N₂O and CO₂ fluxes in bare treatment in two croplands where N₂O flux was higher than at another cropland. Nitrous oxide concentration distribution in soil measured in the conventional treatment showed that N₂O was mainly produced in the surface soil down to 15?cm in the soil. The logarithmic value of the ratio of N₂O flux and nitrate concentration was positively correlated with water filled pore space (WEPS). These results suggest that large N₂O emission in agricultural tropical peatland was caused by denitrification with high decomposition of peat. In addition, N₂O was mainly produced by denitrification at high range of WFPS in surface soil.     

Nitrous oxide emission from soils after incorporating crop residues

Abstract. Emissions of N₂O were measured from different agricultural systems in SE Scotland. N₂O emissions increased temporarily after fertilization of arable crops, cultivation of bare soil, ploughing up of grassland and incorporation of arable and horticultural crop residues, but the effect was short-lived. Most of the emission occurred during the first two weeks, returning to 'background' levels after 30–40 days. The highest flux was from N-rich lettuce residues, 1100 g N₂O-N ha⁻¹ being emitted over the first 14 days after incorporation by rotary tillage. The magnitude and pattern of emissions was strongly influenced by rainfall, soil mineral N, cultivation technique and C:N ratio of the residue. Comparatively large emissions were measured after incorporation of material with low C:N ratios. Management practices are recommended that would increase N-use efficiency and reduce N₂O emissions from agricultural soils.     

Nitrous oxide flux from soil amino acid mineralization

Nitrous oxide (N₂O) is a greenhouse gas produced during microbial transformation of soil N that has been implicated in global climate warming. Nitrous oxide efflux from N fertilized soils has been modeled using NO₃⁻ content with a limited success, but predicting N₂O production in non-fertilized soils has proven to be much more complex. The present study investigates the contribution of soil amino acid (AA) mineralization to N₂O flux from semi-arid soils. In laboratory incubations (−34 kPa moisture potential), soil mineralization of eleven AAs (100 μg AA-N g⁻¹ soil) promoted a wide range in the production of N₂O (156.0±79.3 ng N₂O-N g⁻¹ soil) during 12 d incubations. Comparison of the δ¹³C content (‰) of the individual AAs and the δ¹³C signature of the respired AA-CO₂-C determined that, with the exception of TYR, all of the AAs were completely mineralized during incubations, allowing for the calculation of a N₂O-N conversion rate from each AA. Next, soils from three different semi-arid vegetation ecosystems with a wide range in total N content were incubated and monitored for CO₂ and N₂O efflux. A model utilizing CO₂ respired from the three soils as a measure of organic matter C mineralization, a preincubation soil AA composition of each soil, and the N₂O-N conversion rate from the AA incubations effectively predicted the range of N₂O production by all three soils. Nitrous oxide flux did not correspond to factors shown to influence anaerobic denitrification, including soil NO₃⁻ contents, soil moisture, oxygen consumption, and CO₂ respiration, suggesting that nitrification and aerobic nitrifier denitrification could be contributing to N₂O production in these soils. Results indicate that quantification of AA mineralization may be useful for predicting N₂O production in soils.     

Nitrous oxide emission from soils at low moisture contents

The production of nitrous oxide by soils was studied over short periods at a range of moisture contents up to field capacity with a highly-sensitive gas Chromatographic method.Nitrous oxide (N₂O) was emitted from all soils studied at all soil moisture contents, which ranged from air dry to field capacity. The rate of emission increased with increasing moisture content and with increasing temperature up to 37°C.The evolution of N₂O was not due to displacement of soil air during wetting. It was inhibited by HgCl₂ and toluene, and was prevented by formaldehyde and autoclaving. Thus it appeared to be due to microbiological processes.The results of experiments with nitrification and denitrification inhibitors suggest that a considerable part of the N₂O was produced by the oxidation of ammonia. Production by denitrification of nitrate cannot be ruled out. The relative importance of these two mechanisms probably depends on the moisture and oxygen content of the soil.It is concluded that the microbial production of N₂O is continuous in soil at all moisture contents. The process at low moisture contents constitutes an important component in the cycle which maintains the N₂O concentration in the atmosphere.     

Nitrous oxide emission from a soil under permanent grass: Seasonal and diurnal fluctuations as influenced by manuring and fertilization

The emission of nitrous oxide (N₂O) from soil under grass was measured, following applications of cow slurry and NH₄NO₃ fertilizer. The N₂O-flux from untreated soil averaged 0.58 mg Nm^?2 day^?1 through April to August. Application of slurry at the end of April and at the middle of July caused increases in the daily N₂O-flux of up to 40-fold, compared to untreated grass. Applications of NH₄NO₃ increased the N₂O-flux up to 5 times during the same period. The N₂O-flux often showed marked diurnal fluctuations. These fluctuations are not solely associated with change in temperature, but may also be related to grass root activity and to photosynthesis.     

Nitrous oxide emission from a transplanted rice field in alluvial soil as influenced by management of nitrogen fertiliser

We investigated nitrous oxide (N₂O) emission from an irrigated rice field over two years to evaluate the management of nitrogenous fertiliser and its effect on reducing emissions. Four forms of nitrogenous fertilisers: NPK at the recommended application rate, starch–urea matrix (SUM) + PK, neem‐coated urea + PK and urea alone (urea without coating) were used. Gas samples were collected from the field at weekly intervals with the static chamber technique. N₂O emissions from different treatments ranged from 11.58 to 215.81 N₂O‐N μg/m²/h, and seasonal N₂O emissions from 2.83 to 3.89 kg N₂O‐N/ha. Compared with other fertilisers, N₂O emissions were greatest after the application of the conventional NPK fertiliser. Moreover, SUM + PK reduced total N₂O emissions by 22.33% (P < 0.05) compared with NPK during the rice‐growing period (P < 0.05). The results indicate a strong correlation between N₂O emissions and soil organic carbon, nitrate, ammonium, above‐ and below‐ground plant biomass and photosynthesis (P < 0.05). The application of SUM + PK in rice fields is suitable as a means of reducing N₂O emissions without affecting grain production.     

Nitrous oxide emission as affected by alternate anaerobic and aerobic conditions from soil suspensions enriched with ammonium sulfate

The effect of several anaerobic and aerobic cycles of varying duration on N₂O emission and labelled N loss was investigated in (¹⁵NH₄)₂SO₄ amended soil suspensions. No N₂O was evolved from the continuously-anaerobic treatment. The continuously-aerobic treatment produced approximately 0.8 μg N₂O-N g^?1 dry soil in 56 days. Alternate anaerobic-aerobic cycles increased the net N₂O evolution with 7.2 μg N₂O-N g^?1 dry soil produced in 56 days from the 7-day anaerobic, 7-day aerobic treatment. The net N₂O evolution increased further when the duration of the anaerobic and aerobic periods was increased from 7-7 days to 14-14 days (15.7μg N₂O-N g^?1 dry soil in 56 days), although the total ¹⁵N loss from the system was approximately the same for the two treatments. The results of this study show that N₂O evolution from soils is likely to be greater under fluctuating moisture conditions than under either continuously well-aerated conditions, or continuously excess-moisture conditions.     

Nitrous oxide emission from simulated overland flow wastewater treatment systems

Nitrous oxide evolution was measured from overland flow models receiving daily applications of municipal wastewater with NH₄⁺-N concentration in the wastewater of 10 or 47 μgN ml^?1. The amount of N₂O evolved from the system ranged from 0.07 to 1.3 mg N day^?1, or 1.5–25.5 kg N ha^?1yr^?1, respectively. Liming the soil or increasing the NH₄⁺-N in the wastewater increased the emission of N₂O from the system. The N evolved as N₂O did not exceed 1.2% of the applied NH₄⁺-N, indicating N₂ to be the major denitrification end product in the overland flow wastewater-treatment system.     

Nitrous oxide evolution from structurally intact soil as influenced by tillage and soil water content

Among farmers there is a growing interest for adoption of reduced tillage practices, which has accentuated the need to understand the consequences for soil nutrient dynamics and losses. A laboratory study was conducted with structurally intact soil cores collected from two depths, 0–4 and 14–18 cm, within tillage experiments on contrasting soil types, both experiments with soil under mouldboard ploughing (MP) or shallow tillage (ST). The soil cores were adjusted to one of seven matric potentials ranging from ?1500 to ?15 hPa. The extent and regulation of nitrous oxide (N₂O) evolution as a function of tillage, depth and soil characteristics was studied by measurement of N₂O and CO₂ evolution rates, as well as nitrifying and denitrifying potentials, and subsequent data analysis by multiple linear regression models. At both sites, compaction of ST soil below the depth of tillage was significant. The vertical distribution of N₂O evolution was different in MP and ST soil, but no main effect of tillage on N₂O evolution was observed. Effects of soil variables on N₂O evolution were analysed using volumetric water content, water-filled pore space, or relative gas diffusivity (RD) to represent the effect of soil water. Using RD weakened interactions with tillage and C availability and strengthened main effects, suggesting that RD may provide a more general representation of the water effect. At 0–4 cm depth, N₂O evolution was related to NO₃^? availability in the soil with 5.1% C, but to C availability in the soil with 1.5% C. The contrasting patterns of dependencies in the different environments support the interpretation of reduced tillage and soil water content as indirect controls, via diffusional constraints, of N₂O evolution.     

Nitrous oxide release from arable soil: importance of perennial forage crops

 N₂O emission rates from a sandy loam soil were measured in a field experiment with 2 years of perennial forage crops (ryegrass, ryegrass-red clover, red clover) and 1 year of spring barley cultivation. Spring barley was sown after the incorporation of the forage crop residues. All spring barley plots received 40 kg N ha^–1 N fertiliser. Ryegrass, ryegrass-red clover and red clover plots were fertilised with 350 kg N ha^–1, 175 kg N ha^–1 and 0 kg N ha^–1, respectively. From June 1994 to February 1997, N₂O fluxes were continuously estimated using very large, closed soil cover boxes (5.76 m²). In order to compare the growing crops, the 33 months of investigation were separated into three vegetation periods (March–September) and three winter periods (October–February). All agronomic treatments (fertilisation, harvest and tillage) were carried out during the vegetation period. Large temporal changes were found in the N₂O emission rates. The data were approximately log-normally distributed. Forty-seven percent of the annual N₂O losses were observed to occur during winter, and mainly resulted from N₂O production during daily thawing and freezing cycles. No relationship was found between the N₂O emissions during the winter and the vegetation period. During the vegetation period, N₂O losses and yields were significantly different between the three forage crops. The unfertilised clover plot produced the highest yields and the lowest N₂O losses on this soil compared to the highly fertilised ryegrass plot. Total N₂O losses from soil under spring barley were higher than those from soil under the forage crops; this was mainly a consequence of N₂O emissions after the incorporation of the forage crop residues. Received: 31 October 1997     

Nitrous oxide emissions from boreal organic soil under different land-use

Nitrous oxide emissions were studied with a static chamber technique during 2 years from a drained organic soil in eastern Finland. After drainage, the soil was forested with birch (Betula pendula Roth) and 22 years later, part of the forest was felled and then used for cultivation of barley (Hordeum vulgare L.) and grass. The annual N₂O emissions from the cultivated soil (from 8.3 to 11.0 kg N₂O-N ha⁻¹ year⁻¹) were ca. twice the annual emission from the adjacent forest site (4.2 kg N₂O-N ha⁻¹ year⁻¹). The N₂O emissions from the soils without plants (kept bare by regular cutting or tilling) were also lower (from 6.5 to 7.1 kg N₂O-N ha⁻¹ year⁻¹) than those from the cultivated soil. There was a high seasonal variation in the fluxes with a maximum in spring and early summer. The N₂O fluxes during the winter period accounted for 15-60% of the total annual emissions. N₂O fluxes during the snow-free periods were related to the water table (WT) level, water-filled pore space, carbon mineralisation and the soil temperature. A linear regression model with CO₂ production, WT and soil temperature at the depth of 5 cm as independent variables explained 54% of the variation in the weekly mean N₂O fluxes during the snow-free periods. N₂O fluxes were associated with in situ net nitrification, which alone explained 58% of the variation in the mean N₂O fluxes during the snow-free period. The N₂O-N emissions were from 1.5 to 5% of net nitrification. The acetylene blockage technique indicated that most of the N₂O emitted in the snow-free period originated from denitrification.     

Nitrous oxide and methane emissions from different soil suspensions: effect of soil redox status

Four soil samples from fields of different land use [US (paddy field), China (paddy field) and Belgium (maize and wheat fields)] were incubated as soil suspension (soil:water ratio 1:4) to study the N₂O and CH₄ emission under different soil redox potential conditions. The results show that the N₂O emission was regulated within a narrow redox potential range of +120 to +250 mV, due to the balance of N₂O production and its further reduction to N₂. Methane emission occurred below a soil specific redox potential point, and the emission rates were inversely related to soil redox potentials. Both linear and exponential relationships between CH₄ emission and the soil redox potential were significant. By extrapolating the linear relationship of CH₄ emission against soil redox potential, the critical redox potentials for CH₄ production were estimated at about -170 (US paddy soil), -150 (Chinese paddy soil), -215 (Belgian maize soil), and -195 mV (Belgian wheat soil), respectively. In addition, the results indicate that a soil with a lower critical redox potential for CH₄ production had a higher CH₄ production potential. In this study, N₂O and CH₄ emissions were found to occur at a distinctly different soil redox potential condition. The range of soil redox potential values where both N₂O and CH₄ emissions were low was different for different soils, but it was situated between +120 and -170 mV. This is a wide redox potential range enabling field management practices to minimize both N₂O and CH₄ emissions from wetland ecosystems.     

Nitrous oxide emission from an irrigated cotton field under semiarid subtropical conditions

In a 1-year study, quantification of nitrous oxide (N₂O) emission was made from a flood-irrigated cotton field fertilized with urea at 100kg N ha⁻¹ a⁻¹. Measurements were made during the cotton-growing season (May–November) and the fallow period (December–April). Of the total 95 sampling dates, 77 showed positive N₂O fluxes (range, 0.1 to 33.3g N ha⁻¹ d⁻¹), whereas negative fluxes (i.e., N₂O sink activity) were recorded on 18 occasions (range, −0.1 to −2.2g N ha⁻¹ d⁻¹). Nitrous oxide sink activity was more frequently observed during the growing season (15 out of 57 sampling dates) as compared to the fallow period (3 out of 38 sampling dates). During the growing season, contribution of N₂O to the denitrification gaseous N products was much less (average, 4%) as compared to that during the fallow period (average, 21%). Nitrous oxide emission integrated over the 6-month growing period amounted 324g N ha⁻¹, whereas the corresponding figure for the 6-month fallow period was 648g N ha⁻¹. Subtracting the N₂O sink activity (30.3g N ha⁻¹ and 3.8g N ha⁻¹ during the growing season and fallow period, respectively), the net N₂O emission amounted 938g N ha⁻¹ a⁻¹. Results suggested that high soil moisture and temperature prevailing under flood-irrigated cotton in the Central Punjab region of Pakistan though favor high denitrification rates, but are also conducive to N₂O reduction thus leading to relatively low N₂O emission.