Measuring N2O emissions from organic soils by closed chamber or soil/snow N2O gradient methods

Drained organic soils contribute substantial amounts of nitrous oxide to the global atmosphere, and we should be able to estimate this contribution. We have investigated when the fluxes of N₂O from drained forested or cultivated organic soils could be determined by calculating the fluxes from the concentration gradients of the gas in soil or snow according to Fick's law of diffusion. A static chamber method was applied as a control technique for the gas gradient method. Concentrations of N₂O in soil varied from 296 nl l^?1 to 8534 nl l^?1 during the snow‐free periods and were greatest in the early summer. Our results suggest that the gas gradient method can be used to estimate N₂O emissions from drained organic soils. There was some systematic difference in the N₂O fluxes measured with these two methods, which we attributed to the differences in weather between years 1996 and 1997. In the wet summer of 1996 the chamber method gave greater flux rates than the gas gradient method, and the reverse was true in the dry summer of 1997. In the forest the N₂O fluxes measured with the two methods agreed well. The gas gradient is convenient and fast for measuring N₂O emissions from fairly dry organic unfrozen soil. In winter the diffusion calculation based on the N₂O gradients in snow and the chamber method gave fairly similar flux rates and provided adequate estimates of the fluxes of N₂O in winter.     

Direct field measurement of N2 and N2O evolution from soil

A gas lysimeter has been designed and used to measure directly the evolution of N₂and N₂O in a soil profile under field conditions. Concentrations of N₂ in the soil atmosphere within the lysimeter as low as 2000–5000 p.p.m. have been achieved by flushing with N-free gas. A flow of gas into the base of the lysimeter forms a barrier against diffusion of soil air into the lysimeter during measurements. After reducing the N₂ concentration in the soil core, a low concentration of N₂enriched in N-15 is introduced. By monitoring changes in the 8 N value using a high-precision isotope mass spectrometer, rates of N₂ evolution down to 6 kg N₂-N ha^?1 a^?1 can be detected. N₂O evolution was determined at the same time using the mass spectrometer in the single-beam mode.     

The effect of water table depth on emissions of N2O from a grassland soil

Nitrous oxide (N₂O) emissions were measured by the closed chamber technique from five plots along a transect in a nitrogen‐fertilised grassland, together with soil water content, soil temperature and water table depth, to investigate the effect of water table depth on N₂O emissions. N₂O fluxes varied from <1 g N₂O‐N ha^?1 day^?1 to peaks of around 500–1200 g N₂O‐N ha^?1 day^?1 after N fertiliser applications. There was no significant difference in overall average water table depth between four of the five plots, but significant short‐term temporal variations in water table depth did occur. Rises in the water table were accompanied by exponential increases in N₂O emissions, through the associated increases in the water‐filled pore space of the topsoil. Modelling predicted that if the water table could be managed such that it was kept to no less than 35 cm below the ground surface, fluxes during the growing season would be reduced by 50%, while lowering to 45 cm would reduce them by over 80%. The strong implication of these results is that draining grasslands, so that the water tables are only rarely nearer to the surface than 35 cm when N is available for denitrification, would substantially reduce N₂O emissions.     

Assessment of N2O, NOx and NH3 emissions from a typical rural catchment in Eastern China

To evaluate the atmospheric load of reactive gaseous nitrogen in the fast-developing Eastern China region, we compiled inventories of nitrous oxide (N₂O), nitrogen oxide (NO_x) and ammonia (NH₃) emissions from a typical rural catchment in Jiangsu province, China, situated at the lower reach of the Yangtze River. We considered emissions from synthetic N fertilizer, human and livestock excreta, decomposition of crop residue returned to cropland and residue burning, soil background and household energy consumption. The results showed that, for the 45.5 km² catchment, the annual reactive gaseous emission was 279 ton N, of which 7% was N₂O, 16% was NO_x and 77% was NH₃. Synthetic N fertilizer application was the dominant source of N₂O and NH₃ emissions and crop residue burning was the dominant source of NO_x emission. Sixty-seven percent of the total reactive gaseous N was emitted from croplands, but on a per unit area basis, NO_x and NH₃ emissions in residential areas were higher than in croplands, probably as a result of household crop residue burning and extensive human and livestock excreta management systems. Emission per capita was estimated to be 18.2 kg N year⁻¹ in the rural catchment, and emission per unit area was 56.9 kg N ha⁻¹year⁻¹ for NH₃ + NO_x, which supports the observed high atmospheric N deposition in the catchment. Apparently, efficient use of N fertilizer and biological utilization of crop straw are important measures to reduce reactive gases emissions in this rural catchment.     

Fluxes of N2O from farmed peat soils in Finland

Agricultural peat soils are important sources of nitrous oxide (N₂O). Emissions of N₂O were measured from field plots of grass, barley, potatoes and fallow on a peat field in northern Finland during 2000–2002 and in southern Finland in 1999–2002. In the north the mean annual fluxes of N₂O (with their standard errors) during 2 years were 4.0 (±1.2), 13 (±3.0) and 4.4 (±0.8) kg N ha^?1 from the plots of grass, barley and fallow, respectively. In the north there were no significant thaw periods in the middle of winter. As a result, the thawing in the spring did not induce especially large N₂O emissions. Emissions of N₂O were larger in the south than in the north. In the southern peat field the mean annual fluxes during 3 years were 7.3 (±1.2), 15 (±2.6), 10 (±1.9) and 25 (±6.9) kg N₂O‐N ha^?1 for grass, barley, potato and fallow plots, respectively. Here, the largest single episodes of emission occurred during the spring thaw each year, following winter thaw events. An emission factor of 10.4 kg N₂O‐N ha^?1 year^?1 for the N₂O emission from the decomposition of the peat results from these data if the effect of fertilization according to the IPCC default emission factor is omitted. The direct effect of adding N as fertilizer on N₂O emissions was of minor importance. On average, 52% of the annual N₂O flux entered the atmosphere outside the cropping season (October–April) in the north and 55% in the south. The larger N₂O fluxes from the peat soil in the south might be due to the more humified status of the peat, more rapid mineralization and weather with more cycles of freezing and thawing in the winter.     

Strong pH influence on N2O and CH4 fluxes from forested organic soils

Greenhouse gas (GHG) emissions from farmed organic soils can have a major impact on national emission budgets. This investigation was conducted to evaluate whether afforestation of such soils could mitigate this problem. Over the period 1994–1997, emissions of methane (CH₄) and nitrous oxide (N₂O) were recorded from an organic soil site in Sweden, forested with silver birch (Betula pendula Roth), using static field chambers. The site was used for grazing prior to forestation. Soil pH and soil carbon content varied greatly across the site. The soil pH ranged from 3.6 to 5.9 and soil carbon from 34 to 42%. The mean annual N₂O emission was 19.4 (± 6.7) kg N₂O‐N ha^?1 and was strongly correlated with soil pH (r = ?0.93, P < 0.01) and soil carbon content (r = 0.97, P < 0.001). The N₂O emissions showed large spatial and temporal variability with greatest emissions during the summer periods. The site was a sink for CH₄ (i.e. ?0.8 (± 0.5) kg CH₄ ha^?1 year^?1) and the flux correlated well with the C/N ratio (r = 0.93, P < 0.01), N₂O emission (r = 0.92, P < 0.01), soil pH (r = ?0.95, P < 0.01) and soil carbon (r = 0.97, P < 0.001). CH₄ flux followed a seasonal pattern, with uptake dominating during the summer, and emission during winter. This study indicates that, because of the large N₂O emissions, afforestation may not mitigate the GHG emissions from fertile peat soils with acidic pH, although it can reduce the net GHG because of greater CO₂ assimilation by the trees compared with agricultural crops.     

Mitigation of N2O emissions from grassland by nitrification inhibitor and Actilith F2 applied with fertilizer and cattle slurry

Abstract. Nitrous oxide (N₂O) is involved in both ozone destruction and global warming. In agricultural soils it is produced by nitrification and denitrification mainly after fertilization. Nitrification inhibitors have been proposed as one of the management tools for the reduction of the potential hazards of fertilizer-derived N₂O. Addition of nitrification inhibitors to fertilizers maintains soil N in ammonium form, thereby gaseous N losses by nitrification and denitrification are less likely to occur and there is increased N utilization by the sward. We present a study aimed to evaluate the effectiveness of the nitrification inhibitor dicyandiamide (DCD) and of the slurry additive Actilith F2 on N₂O emissions following application of calcium ammonium nitrate or cattle slurry to a mixed clover/ryegrass sward in the Basque Country. The results indicate that large differences in N₂O emission occur depending on fertilizer type and the presence or absence of a nitrification inhibitor. There is considerable scope for immediate reduction of emissions by applying DCD with calcium ammonium nitrate or cattle slurry. DCD, applied at 25 kg ha^–1, reduced the amount of N lost as N₂O by 60% and 42% when applied with cattle slurry and calcium ammonium nitrate, respectively. Actilith F2 did not reduce N₂O emissions and it produced a long lasting mineralization of previously immobilized added N.     

CH4 oxidation and N2O emissions at varied soil water-filled pore spaces and headspace CH4 concentrations

Emission of N₂O and CH₄ oxidation rates were measured from soils of contrasting (30-75%) water-filled pore space (WFPS). Oxidation rates of ¹³C-CH₄ were determined after application of 10 μl ¹³C-CH₄ l⁻¹ (10 at. % excess ¹³C) to soil headspace and comparisons made with estimates from changes in net CH₄ emission in these treatments and under ambient CH₄ where no ¹³C-CH₄ had been applied. We found a significant effect of soil WFPS on ¹³C-CH₄ oxidation rates and evidence for oxidation of 2.2 μg ¹³C-CH₄ d⁻¹ occurring in the 75% WFPS soil, which may have been either aerobic oxidation occurring in aerobic microsites in this soil or anaerobic CH₄ oxidation. The lowest ¹³C-CH₄ oxidation rate was measured in the 30% WFPS soil and was attributed to inhibition of methanotroph activity in this dry soil. However, oxidation was lowest in the wetter soils when estimated from changes in concentration of ¹²⁺¹³C-CH₄. Thus, both methanogenesis and CH₄ oxidation may have been occurring simultaneously in these wet soils, indicating the advantage of using a stable isotope approach to determine oxidation rates. Application of ¹³C-CH₄ at 10 μl ¹³C-CH₄ l⁻¹ resulted in more rapid oxidation than under ambient CH₄ conditions, suggesting CH₄ oxidation in this soil was substrate limited, particularly in the wetter soils. Application of and (80 mg N kg soil⁻¹; 9.9 at.% excess ¹⁵N) to different replicates enabled determination of the respective contributions of nitrification and denitrification to N₂O emissions. The highest N₂O emission (119 μg ¹⁴⁺¹⁵N-N₂O kg soil⁻¹ over 72 h) was measured from the 75% WFPS soil and was mostly produced during denitrification (18.1 μg ¹⁵N-N₂O kg soil⁻¹; 90% of ¹⁵N-N₂O from this treatment). Strong negative correlations between ¹⁴⁺¹⁵N-N₂O emissions, denitrified ¹⁵N-N₂O emissions and ¹³C-CH₄ concentrations (r=−0.93 to −0.95, N₂O; r=−0.87 to −0.95, denitrified ¹⁵N-N₂O; P<0.05) suggest a close relationship between CH₄ oxidation and denitrification in our soil, the nature of which requires further investigation.     

Mitigation options for N2O emission from a corn field in Kalimantan, Indonesia

Field experiments were designed to quantify N₂O emissions from corn fields after the application of different types of nitrogen fertilizers. Plots were established in South Kalimantan, Indonesia, and given either urea (200 kg ha⁻¹), urea (170 kg ha⁻¹) + dicyandiamide ([DCD] 20 kg ha⁻¹) or controlled-release fertilizer LP-30 (214 kg ha⁻¹) prior to the plantation of corn seeds (variety BISI 2). Each fertilizer treatment was equivalent to 90 kg N ha⁻¹. Plots without chemical N fertilizer were also prepared as a control. The field was designed to have three replicates for each treatment with a randomized block design. Nitrous oxide fluxes were measured at 4, 8, 12, 21, 31, 41, 51, 72 and 92 days after fertilizer application (DAFA). Total N₂O emission was the highest from the urea plots, followed by the LP-30 plots. The emissions from the urea + DCD plots did not differ from those from the control plots. The N₂O emission from the urea + DCD plots was approximately one thirtieth of that from the urea treatment. However, fertilizer type had no effect on grain yield. Thus, the use of urea + DCD is considered to be the best mitigation option among the tested fertilizer applications for N₂O emission from corn fields in Kalimantan, Indonesia.     

Brief and vigorous N2O production by soil at spring thaw

In an acid sandy loam soil (pH 3.8), field production of N²O was two orders of magnitude higher at thaw in the spring than at any time during the rest of the year. Soil thaw in midwinter did not result in any increase in N²O flux. Soil water content remained at, or above field capacity during measurements; nitrate was added in excess. This effect could be reproduced in the laboratory: thawing soil cores at controlled temperature, nitrate and moisture yielded a large flush of N²O compared to an unfrozen control. The results indicate the importance of microbial N²O production during thaw for total annual N²O-emission.     

The influence of tillage on NO and N2O fluxes under spring and winter barley

Abstract. There is a lack of information about the influence of tillage and time of sowing on N₂O and NO emission in cereal production. Both factors influence crop growth and soil conditions and thereby can affect trace gas emissions from soils. We measured fluxes of NO and N₂O in a tillage experiment where grassland on clay loam soil was converted to arable by either direct drilling or ploughing to 30 cm depth. We made measurements in spring for 20 days after fertilizer application to spring-sown and to winter-sown barley. Both were the second barley crop after grass. Direct drilling enhanced N₂O emission primarily as a result of restricted gas diffusivity causing poor aeration after rainfall. Deep ploughing enhanced NO emission, because of the large air-filled porosity in the topsoil. NO and N₂O emissions were smaller from winter sown crops than from spring sown crops.   The three rates of N fertilizer application (40, 80 or 120 kg N ha^–1) did not produce the expected linear response in either soil available N concentrations or in NO and N₂O fluxes. We attributed this to the lack of rainfall in the ten-day period after fertilizer application and therefore very slow incorporation and movement of fertilizer into and through the soil.     

Effects of Plant Species on CH4 and N2O Fluxes from a Volcanic Grassland Soil in Nasu, Japan

To investigate the effects of plant species in grassland on methane (CH₄) and nitrous oxide (N₂O) fluxes from soil, fluxes from an orchardgrass ( Dactylis glomerata L.) grassland, white clover ( Trifolium repens L.) grassland and orchardgrass/white clover mixed grassland were measured weekly from April 2001 to March 2002 using a vented closed chamber method. Related environmental parameters (soil inorganic N content, soil pH (H₂O) value, soil moisture content, soil temperature, grass yield, and the number of soil microorganisms) were also regularly monitored. On an annual basis, CH₄ consumption in the soil of the orchardgrass grassland, white clover grassland and orchardgrass/white clover mixed grassland was 1.8, 2.4, and 1.8 kg C ha⁻¹ year⁻¹, respectively. The soil bulk density of the white clover grassland was lower than that of the other grasslands. Fluxes of CH₄ were positively correlated with the soil moisture content. White clover increased the CH₄ consumption by improving soil aeration. Nitrogen supply to the soil by white clover did not decrease the CH₄ consumption in the soil of our grasslands. On the other hand, annual N₂O emissions from the orchardgrass grassland, white clover grassland, and orchardgrass/white clover mixed grassland were 0.39, 1.59, and 0.67 kg N ha⁻¹ year⁻¹, respectively. Fluxes of N₂O were correlated with the NO₃⁻ content in soil and soil temperature. White clover increased the N₂O emissions by increasing the inorganic N content derived from degrading white clover in soil in summer.     

Isotopologue fractionation during microbial reduction of N2O within soil mesocosms as a function of water-filled pore space

Isotopologue analyses of N₂O within soil mesocosm experiments were used to evaluate the influence of N₂O reduction on isotope fractionation. We investigated fractionation during N₂O reduction at 60%, 80% and 100% water-filled pore space (WFPS) and found net isotope effects (NIE) for δ¹⁵N of 4.2–7.8‰, δ¹⁸O of 12.5–19.1‰, δ¹⁵N^α of 6.4–9.7‰ and δ¹⁵N^β of 2.0–5.9‰. Consequently, N₂O reduction has a marked affect on isotopologue values and the importance of this process in flux chamber studies should not be ignored. With the exception of SP (the difference between the δ¹⁵N of the central, α, and terminal, β, atoms) inverse relationships between the NIE, reaction rate and reaction rate constant and WFPS were observed. Isotopic discrimination in SP during N₂O reduction was small and the average NIE for the treatments varied between 2.9‰ and 4.5‰. A strong correlation was evident between δ¹⁸O vs. δ¹⁵N and δ¹⁸O vs. δ¹⁵N^α during reduction with slopes of 2.6 and 1.9, respectively, which contrasts from a slope of <1 commonly observed for mixing between soil-derived and atmospheric N₂O in flux chambers.