Soil N<Subscript>2</Subscript>O emissions and N<Subscript>2</Subscript>O/(N<Subscript>2</Subscript>O+N<Subscript>2</Subscript>) ratio as affected by different fertilization practices and soil moisture

The objective of this work was to evaluate the effect of the chemical nature and application frequency of N fertilizers at different moisture contents on soil N₂O emissions and N₂O/(N₂O+N₂) ratio. The research was based on five fertilization treatments: unfertilized control, a single application of 80 kg ha⁻¹ N-urea, five split applications of 16 kg ha⁻¹ N-urea, a single application of 80 kg ha⁻¹ N–KNO₃, five split applications of 16 kg ha⁻¹ N–KNO₃. Cumulative N₂O emissions for 22 days were unaffected by fertilization treatments at 32% water-filled pore space (WFPS). At 100% and 120% WFPS, cumulative N₂O emissions were highest from soil fertilized with KNO₃. The split application of N fertilizers decreased N₂O emissions compared to a single initial application only when KNO₃ was applied to a saturated soil, at 100% WFPS. Emissions of N₂O were very low after the application of urea, similar to those found at unfertilized soil. Average N₂O/(N₂O+N₂) ratio values were significantly affected by moisture levels (p = 0.015), being the lowest at 120% WFPS. The N₂O/(N₂O+N₂) ratio averaged 0.2 in unfertilized soil and 0.5 in fertilized soil, although these differences were not statistically significant.     

Nitrous oxide emissions from two dairy pasture soils as affected by different rates of a fine particle suspension nitrification inhibitor, dicyandiamide

In grazed pasture systems, a major source of N₂O is nitrogen (N) returned to the soil in animal urine. We report in this paper the effectiveness of a nitrification inhibitor, dicyandiamide (DCD), applied in a fine particle suspension (FPS) to reduce N₂O emissions from dairy cow urine patches in two different soils. The soils are Lismore stony silt loam (Udic Haplustept loamy skeletal) and Templeton fine sandy loam (Udic Haplustepts). The pasture on both soils was a mixture of perennial ryegrass (Lolium perenne) and white clover (Trifolium repens). Total N₂O emissions in the Lismore soil were 23.1–31.0 kg N₂O-N ha⁻¹ following the May (autumn) and August (late winter) urine applications, respectively, without DCD. These were reduced to 6.2–8.4 kg N₂O-N ha⁻¹ by the application of DCD FPS, equivalent to reductions of 65–73%. All three rates of DCD applied (7.5, 10 and 15 kg ha⁻¹) were effective in reducing N₂O emissions. In the Templeton soil, total N₂O emissions were reduced from 37.4 kg N₂O-N ha⁻¹ without DCD to 14.6–16.3 kg N₂O-N ha⁻¹ when DCD was applied either immediately or 10 days after the urine application. These reductions are similar to those in an earlier study where DCD was applied as a solution. Therefore, treating grazed pasture soils with an FPS of DCD is an effective technology to mitigate N₂O emissions from cow urine patch areas in grazed pasture soils.     

N<Subscript>2</Subscript>O emission from conventional and minimum-tilled soils

In this study, we investigated N₂O emissions from two fields under minimum tillage, cropped with maize (MT maize) and summer oats (MT oats), and a conventionally tilled field cropped with maize (CT maize). Nitrous oxide losses from the MT maize and MT oats fields (5.27 and 3.64 kg N₂O-N ha⁻¹, respectively) were significantly higher than those from the CT maize field (0.27 kg N₂O-N ha⁻¹) over a period of 1 year. The lower moisture content in CT maize (43% water-filled pore space [WFPS] compared to 60–65%) probably caused the difference in total N₂O emissions. Denitrification was found to be the major source of N₂O loss. Emission factors calculated from the MT field data were high (0.04) compared to the CT field (0.001). All data were simulated with the denitrification decomposition model (DNDC). For the CT field, N₂O and N₂O + N₂ emissions were largely overestimated. For the MT fields, there was a better agreement with the total N₂O and N₂O + N₂ emissions, although the N₂O emissions from the MT maize field were underestimated. The simulated N₂O emissions were particularly influenced by fertilization, but several other measured N₂O emission peaks associated with other management practices at higher WFPS were not captured by the model. Several mismatches between simulated and measured \textNH₄⁺ {\text{NH}}_4^ + , \textNO₃^- {\text{NO}}_3^ - and WFPS for all fields were observed. These mismatches together with the insensitivity of the DNDC model for increased N₂O emissions at the management practices different from fertilizer application explain the limited similarity between the simulated and measured N₂O emissions pattern from the MT fields.     

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.     

Nitrous oxide production in turfgrass systems: Effects of soil properties and grass clipping recycling

Soil N₂O emissions can affect global environments because N₂O is a potent greenhouse gas and ozone depletion substance. In the context of global warming, there is increasing concern over the emissions of N₂O from turfgrass systems. It is possible that management practices could be tailored to reduce emissions, but this would require a better understanding of factors controlling N₂O production. In the present study we evaluated the spatial variability of soil N₂O production and its correlation with soil physical, chemical and microbial properties. The impacts of grass clipping addition on soil N₂O production were also examined. Soil samples were collected from a chronosequence of three golf courses (10, 30, and 100-year-old) and incubated for 60 days at either 60% or 90% water filled-pore space (WFPS) with or without the addition of grass clippings or wheat straw. Both soil N₂O flux and soil inorganic N were measured periodically throughout the incubation. For unamended soils, cumulative soil N₂O production during the incubation ranged from 75 to 972 ng N g⁻¹ soil at 60% WFPS and from 76 to 8842 ng N g⁻¹ soil at 90% WFPS. Among all the soil physical, chemical and microbial properties examined, soil N₂O production showed the largest spatial variability with the coefficient of variation ~110% and 207% for 60% and 90% WFPS, respectively. At 60% WFPS, soil N₂O production was positively correlated with soil clay fraction (Pearson's r = 0.91, P < 0.01) and soil NH₄⁺–N (Pearson's r = 0.82, P < 0.01). At 90% WFPS, however, soil N₂O production appeared to be positively related to total soil C and N, but negatively related to soil pH. Addition of grass clippings and wheat straw did not consistently affect soil N₂O production across moisture treatments. Soil N₂O production at 60% WFPS was enhanced by the addition of grass clippings and unaffected by wheat straw (P < 0.05). In contrast, soil N₂O production at 90% WFPS was inhibited by the addition of wheat straw and little influenced by glass clippings (P < 0.05), except for soil samples with >2.5% organic C. Net N mineralization in soil samples with >2.5% organic C was similar between the two moisture regimes, suggesting that O₂ availability was greater than expected from 90% WFPS. Nonetheless, small and moderate changes in the percentage of clay fraction, soil organic matter content, and soil pH were found to be associated with large variations in soil N₂O production. Our study suggested that managing soil acidity via liming could substantially control soil N₂O production in turfgrass systems.     

Plant material addition affects soil nitrous oxide production differently between aerobic and oxygen-limited conditions

It is a common agricultural practice for crop residues to be plowed into the soil or left on the soil surface. Soil addition of crop residues can considerably modify soil microbial activity and net N mineralization, and in general such modifications are negatively related to the C:N ratios of crop residues. Yet, little is known on the impacts of crop residues of different C:N ratios on soil nitrous oxide (N₂O) production under different aeration conditions via nitrification and denitrification. In this study, an 84-day laboratory incubation was conducted under aerobic and O₂-limited conditions and soil N₂O production was measured every 3 days after the addition of plant materials with a wide range of C:N ratios from 14 to 297. Two aerobic conditions were created by adjusting the water content of soil at a bulk density of 1.1 g cm⁻³ to 30% water-filled pore space (WFPS) and 60% WFPS, and two O₂-limited conditions were made by 90% WFPS and fluctuation between 90% and 30% WFPS. Each fluctuation cycle lasted 9 days and soil water content was readjusted to 90% WFPS at the end of each cycle. We also measured microbial respiration activity and net N mineralization periodically (i.e., 3, 7, 14, 28, 42, 56, 70, and 84 days) during the incubation and microbial biomass C at the end of incubation. At aerobic conditions, soil amendments of plant materials, regardless of their C:N ratios, all enhanced soil N₂O production. However, net N mineralization was dependent on plant material C:N ratios, being significantly higher or lower than the control for C:N ratios ∼15 and C:N ratios ≥44, respectively. Such inconsistent responses indicated that nitrifiers mediating nitrification and therefore byproduct N₂O production could strongly compete with heterotrophic microbes for NH₄⁺ and therefore net N mineralization was not a good predictor for nitrification-associated N₂O production. Interestingly, plant material additions reduced soil N₂O production by up to ∼95% at O₂-limited conditions, perhaps due to NO₃⁻ limitation. Soil NO₃⁻ production via nitrification could be low at O₂-limited conditions, and soil NO₃⁻ availability could be further reduced due to increases in microbial biomass and thus microbial N assimilation after plant material additions. This NO₃⁻ limitation might enhance N₂O reduction to N₂, by which denitrifiers could harvest more energy from the consumption of limited NO₃⁻. Nonetheless, our results revealed contrasting differences in N₂O production between aerobic and O₂-limited conditions following soil amendments of plant materials.     

Effects of moisture and temperature on greenhouse gas emissions and C and N leaching losses in soil treated with biogas slurry

The objective of this study was to examine the effects of soil moisture, irrigation pattern, and temperature on gaseous and leaching losses of carbon (C) and nitrogen (N) from soils amended with biogas slurry (BS). Undisturbed soil cores were amended with BS (33 kg N ha⁻¹) and incubated at 13.5°C and 23.5°C under continuous irrigation (2 mm day⁻¹) or cycles of strong irrigation and partial drying (every 6 weeks, 1 week with 12 mm day⁻¹). During the 6 weeks after BS application, on average, 30% and 3.8% of the C and N applied with BS were emitted as carbon dioxide (CO₂) and nitrous oxide (N₂O), respectively. Across all treatments, a temperature increase of 10°C increased N₂O and CO₂ emissions by a factor of 3.7 and 1.7, respectively. The irrigation pattern strongly affected the temporal production of CO₂ and N₂O but had no significant effect on the cumulative production. Nitrogen was predominantly lost in the form of nitrate (NO₃⁻). On average, 16% of the N applied was lost as NO₃⁻. Nitrate leaching was significantly increased at the higher temperature (P < 0.01), while the irrigation pattern had no effect (P = 0.63). Our results show that the C and N turnovers were strongly affected by BS application and soil temperature whereas irrigation pattern had only minor effects. A considerable proportion of the C and N in BS were readily available for soil microorganisms.     

Influence of drip and furrow irrigation systems on nitrogen oxide emissions from a horticultural crop

Irrigation management has an important influence on emissions of nitrous oxide (N₂O) and nitric oxide (NO) from irrigated agricultural soils. In order to develop strategies to reduce the emission of these gases, a field experiment was carried out to compare the influence of different irrigation systems: furrow (FI) and drip-irrigation (DI), on N₂O and NO emissions from a soil during the melon crop season. Two fertilizer treatments were evaluated for each irrigation regime: ammonium sulphate (AS) as a mineral N fertilizer, at a rate of 175 kg N ha^?1; and a control without any N fertilizer (Control). On plots where the AS treatment was applied, drip irrigation reduced total N₂O and NO emissions (by 70% and 33% respectively) with respect to values for furrow irrigation. This was probably due to the lower amount of water applied and the different soil wetting pattern associated with DI. Dry areas of the drip-irrigated plots emitted a similar amount of N₂O to the wet areas (0.45 kg N₂O-N ha^?1) in the Control and greater quantities in the AS treatment (0.92 kg N₂O-N ha^?1 for dry and 0.70 kg N₂O-N ha^?1 for wet areas). We suggest that the N oxide pulses observed throughout the irrigation period on DI plots could have been the result of frequent increases in the soil wetting volume after the addition of water. Denitrification losses (from depths of 0–10 cm) were estimated at 11.44 kg N₂O- N ha^?1 for the AS treatment under FI and at 4.96 kg N₂O-N ha^?1 for DI. Under DI, nitrification was an important source of N₂O, whereas denitrification was the most important source under FI. The addition of NH₄⁺ and the use of DI enhanced the N₂O/N₂ ratio of gases produced through denitrification. The quantity of dissolved organic C (DOC) in the soil generally decreased with addition of NH₄⁺.This work showed that, in comparison with furrow irrigation, drip irrigation is a method that can be used to save water and mitigate emissions of the atmospheric pollutants NO and N₂O.     

Effect of improved fallow on crop productivity, soil fertility and climate-forcing gas emissions in semi-arid conditions

The impacts of fallow on soil fertility, crop production and climate-forcing gas emissions were determined in two contrasting legumes, Gliricidia sepium and Acacia colei, in comparison with traditional unamended fallow and continuous cultivation systems. After 2 years, the amount of foliar material produced did not differ between the two improved fallow species; however, grain yield was significantly elevated by 55% in the first and second cropping season after G. sepium compared with traditional fallow. By contrast, relative to the unamended fallow, a drop in grain yield was observed in the first cropping season after A. colei, followed by no improvement in the second. G. sepium had higher foliar N, K and Mg, while A. colei had lower foliar N but higher lignin and polyphenols. In the third year after fallow improvement, a simulated rainfall experiment was performed on soils to compare efflux of N₂O and CO₂. Improved fallow effects on soil nutrient composition and microbial activity were demonstrated through elevated N₂O and CO₂ efflux from soils in G. sepium fallows compared with other treatments. N₂O emissions were around six times higher from this nitrogen-fixing soil treatment, evolving 69.9 ngN₂O–N g⁻¹soil h⁻¹ after a simulated rainfall event, compared with only 8.5 and 4.8 ngN₂O–N g⁻¹soil h⁻¹ from soil under traditional fallow and continuous cultivation, respectively. The findings indicate that selection of improved fallows for short-term fertility enhancement has implications for regional N₂O emissions for dry land regions.     

Nitrous oxide emission from different fertilizers and its mitigation by nitrification inhibitors in irrigated rice

 N₂O emissions from a transplanted irrigated rice grown on a Typic Ustochrept soil at New Delhi, India, were studied to evaluate the effect of N fertilizers, i.e. urea and (NH₄)₂SO₄, alone and in combination with the nitrification inhibitors dicyandiamide (DCD) and thiosulphate. The addition of urea and (NH₄)₂SO₄ increased N₂O emissions considerably when compared to no fertilizer N application (control). N₂O measurement in the field was done by a closed-chamber method for a period of 98 days. The application of urea with DCD and thiosulphate reduced N₂O fluxes considerably. The highest total N₂O-N emission (235 g N₂O-N ha^–1) was from the (NH₄)₂SO₄ treatment, which was significantly higher than the total N₂O-N emission from the urea treatment (160 g N₂O-N ha^–1). DCD reduced N₂O-N emissions by 11% and 26% when applied with urea and(NH₄)₂SO₄, respectively, whereas thiosulphate in combination with urea reduced N₂O-N emissions by 9%. Total N₂O-N emissions were found to range from 0.08% to 0.14% of applied N. N₂O emissions were low during submergence and increased substantially during drainage of standing water. Received: 20 October 1999     

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 feedlot manure and green waste compost applied to Vertisols

Application of feedlot manure (FLM) to cropping and grazing soils could provide a valuable N nutrient resource. However, because of its high but variable N concentration, FLM has the potential for environmental pollution of water bodies and N₂O emission to the atmosphere. As a potential management tool, we utilised the low-nutrient green waste compost (GWC) to assess its effectiveness in regulating N release and the amount of N₂O emission from two Vertisols when both FLM and GWC were applied together. Cumulative soil N₂O emission over 32 weeks at 24°C and field capacity (70% water-filled pore space) for a black Vertisol (Udic Paleustert) was 45 mg N₂O m⁻² from unamended soil. This increased to 274 mg N₂O m⁻² when FLM was applied at 1 kg m⁻² and to 403 mg N₂O m⁻² at 2 kg m⁻². In contrast, the emissions of 60 mg N₂O m⁻² when the soil was amended with GWC 1 kg m⁻² and 48 mg N₂O m⁻² at 2 kg m⁻² were not significantly greater than the unamended soil. Emission from a mixture of FLM and GWC applied in equal amounts (0.5 kg m⁻²) was 106 mg N₂O m⁻² and FLM applied at 0.5 kg m⁻² and GWC at 1.5 kg GWC m⁻² was 117 mg N₂O m⁻². Although cumulative N₂O emissions from an unamended grey Vertisol (Typic Chromustert) were only slightly higher than black Vertisol (57 mg N₂O m⁻²), FLM application at 1 kg m⁻² increased N₂O emissions by 14 times (792 mg N₂O m⁻²) and at 2 kg m⁻² application by 22 times (1260 mg N₂O m^-2). Application of GWC did not significantly increase N₂O emission (99 mg N₂O m⁻² at 1 kg m⁻² and 65 mg N₂O m⁻² at 2 kg m⁻²) above the unamended soil. As observed for the black Vertisol, a mixture of FLM (0.5 kg m⁻²) and GWC (0.5 or 1.5 kg m⁻²) reduced N₂O emission by >50% of that from the FLM alone, most likely by reducing the amount of mineral N (NH₄⁺–N and NO₃⁻–N) in the soil, as mineral N in soil and the N₂O emission were closely correlated.     

Responses of soil organic matter and greenhouse gas fluxes to soil management and land use changes in a humid temperate region of southern Europe

We studied the effects of soil management and changes of land use on soils of three adjacent plots of cropland, pasture and oak (Quercus robur) forest. The pasture and the forest were established in part of the cropland, respectively, 20 and 40 yr before the study began. Soil organic matter (SOM) dynamics, water-filled pore space (WFPS), soil temperature, inorganic N and microbial C, as well as fluxes of CO₂, CH₄ and N₂O were measured in the plots over 25 months. The transformation of the cropland to mowed pasture slightly increased the soil organic and microbial C contents, whereas afforestation significantly increased these variables. The cropland and pasture soils showed low CH₄ uptake rates (<1 kg C ha⁻¹ yr⁻¹) and, coinciding with WFPS values >70%, episodes of CH₄ emission, which could be favoured by soil compaction. In the forest site, possibly because of the changes in soil structure and microbial activity, the soil always acted as a sink for CH₄ (4.7 kg C ha⁻¹ yr⁻¹). The N₂O releases at the cropland and pasture sites (2.7 and 4.8 kg N₂O-N ha⁻¹ yr⁻¹) were, respectively, 3 and 6 times higher than at the forest site (0.8 kg N₂O-N ha⁻¹ yr⁻¹). The highest N₂O emissions in the cultivated soils were related to fertilisation and slurry application, and always occurred when the WFPS >60%. These results show that the changes in soil properties as a consequence of the transformation of cropfield to intensive grassland do not imply substantial changes in SOM or in the dynamics of CH₄ and N₂O. On the contrary, afforestation resulted in increases in SOM content and CH₄ uptake, as well as decreases in N₂O emissions.     

Nitrous oxide emissions from cattle-impacted pasture soil amended with nitrate and glucose

There is little information concerning N₂O fluxes in the pasture soil that has received large amounts of nutrients, such as urine and dung, for several years. The aims of this study were to (1) experimentally quantify the relationship between mineral N input and N₂O emissions from denitrification, (2) describe the time course of N₂O fluxes resulting in N inputs, and (3) find whether there exists an upper limit of the amount of nitrogen escaping the soil in the form of N₂O. The study site was a grassland used as a cattle overwintering area. It was amended with KNO₃ and glucose corresponding to 10–1,500 kg N and C per hectare, covering the range of nutrient inputs occurring in real field conditions. Using manual permanent chambers, N₂O fluxes from the soil were monitored for several days after the amendments. The peak N₂O emissions were up to 94 mg N₂O–N m⁻² h⁻¹, 5–8 h after amendment. No upper limit of N₂O emissions was detected as the emissions were directly related to the dose of nutrients in the whole range of amendments used, but the fluxes reflected the soil and environmental conditions, too. Thus, in three different experiments performed during the season, the total cumulative losses of N₂O–N ranged from 0.2 to 5.6% of the applied 500kg ha⁻¹. Splitting of high nutrient doses lowered the rate of N₂O fluxes after the first amendment, but the effect of splitting on the total amount of N₂O–N released from the soil was insignificant, as the initial lower values of emissions in the split variants were compensated for by a longer duration of gas fluxes. The results suggest that the cattle-impacted soil has the potential to metabolize large inputs of mineral nitrogen over short periods (∼days). Also, the emission factors for did not exceed values reported in literature.     

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.     

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.     

Dissolved organic matter and inorganic N jointly regulate greenhouse gases fluxes from forest soils with different moistures during a freeze-thaw period

ABSTRACT

Antecedent soil moisture before freezing can affect greenhouse gases (GHG) fluxes from soils during thaw, but their critical threshold values for GHG fluxes and the underlying mechanisms are still not clear. By using packed soil-core incubation experiments, we have studied nitrous oxide (N₂O), carbon dioxide (CO₂) and methane (CH₄) fluxes from a mature broadleaf and Korean pine-mixed forest soil and an adjacent white birch forest soil with nine levels of soil moisture ranging from 10 to 90% water-filled pore space (WFPS) during a 2-month freezing at ?8°C and the following 10-day thaw at 10°C. The threshold values of soil moisture ranged from 50 to 70% WFPS for CH₄ uptake and from 70 to 90% WFPS for N₂O and CO₂ emissions from the two soils during the freeze-thaw period. Under the optimum soil moisture condition, fulvic-like compounds with high bioavailability contributed more than 60% of dissolved organic matter (DOM) in the soil. Cumulative N₂O emissions from forest soils during the freeze-thaw period were greatest when the concentration ratio of nitrate-N to dissolved organic carbon (DOC) was 0.04 g N g^?1 C. Cumulative soil CO₂ emissions and CH₄ uptake during the freeze-thaw period were both regulated by the interaction between soil DOC and net N mineralization. The activities of β-1,4-glucosidase and β-1,4-N-acetyl-glucosaminidase, microbial biomass C and N, and the microbial biomass C-to-N ratios, were all significantly correlated to the soil N₂O, CO₂, and CH₄ fluxes. Overall, upon a freeze-thaw period with different soil moistures, GHG fluxes from forest soils were jointly regulated by inorganic N and DOC concentrations, and related to the labile components of DOM released into the soil, which could be strictly controlled by the related microbial properties.     

Short-term effects of ammonium nitrogen in upland pasture soil affected or not affected by cattle

The short-term effects of excessive NH₄⁺-N on selected characteristics of soil unaffected (low annual N inputs) and affected (high annual N inputs) by cattle were investigated under laboratory conditions. The major hypothesis tested was that above a theoretical upper limit of NH₄⁺ concentration, an excess of NH₄⁺-N does not further increase NO₃⁻ formation rate in the soil, but only supports accumulation of NO₂⁻-N and gaseous losses of N as N₂O. Soils were amended with 10 to 500 μg NH₄⁺-N g⁻¹ soil. In both soils, addition of NH₄⁺-N increased production of NO₃⁻-N until some limit. This limit was higher in cattle-affected soil than in unaffected soil. Production of N₂O increased in the whole range of amendments in both soils. At the highest level of NH₄⁺-N addition, NO₂⁻-N accumulated in cattle-affected soil while NO₃⁻-N production decreased in cattle-unaffected soil. Despite being statistically significant, observed effects of high NH₄⁺-N addition were relatively weak. Uptake of mineral N, stimulated by glucose amendment, decreased the mineral N content in both soils, but it also greatly increased production of N₂O.     

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.     

Spatial variability and biophysicochemical controls on N<Subscript>2</Subscript>O emissions from differently tilled arable soils

Nitrous oxide (N₂O) emissions, soil microbial community structure, bulk density, total pore volume, total C and N, aggregate mean weight diameter and stability index were determined in arable soils under three different types of tillage: reduced tillage (RT), no tillage (NT) and conventional tillage (CT). Thirty intact soil cores, each in a 25 × 25-m² grid, were collected to a depth of 10 cm at the seedling stage of winter wheat in February 2008 from Maulde (50°3′ N, 3°43′ W), Belgium. Two additional soil samples adjacent to each soil core were taken to measure the spatial variance in biotic and physicochemical conditions. The microbial community structure was evaluated by means of phospholipid fatty acids analysis. Soil cores were amended with 15 kg NO₃⁻-N ha⁻¹, 15 kg NH₄⁺-N ha⁻¹ and 30 kg ha⁻¹ urea-N ha⁻¹ and then brought to 65% water-filled pore space and incubated for 21 days at 15°C, with regular monitoring of N₂O emissions. The N₂O fluxes showed a log-normal distribution with mean coefficients of variance (CV) of 122%, 78% and 90% in RT, NT and CT, respectively, indicating a high spatial variation. However, this variability of N₂O emissions did not show plot scale spatial dependence. The N₂O emissions from RT were higher (p < 0.01) than from CT and NT. Multivariate analysis of soil properties showed that PC1 of principal component analysis had highest loadings for aggregate mean weight diameter, total C and fungi/bacteria ratio. Stepwise multiple regression based on soil properties explained 72% (p < 0.01) of the variance of N₂O emissions. Spatial distributions of soil properties controlling N₂O emissions were different in three different tillages with CV ranked as RT > CT > NT.