Emission of NH3 and N2O after spreading of pig slurry by broadcasting or band spreading

Abstract. The recommended method of reducing the emission of NH₃ while spreading manure is to plough or harrow the manure into the soil. This in turn increases the possibility of N₂O emission. At two sites in southern Sweden emissions of NH₃ and N₂O were measured after spreading pig slurry by broadcasting and band spreading. The band spreading technique can be used in growing crops i.e. when nitrogen is most needed, and it is thought that the NH₃ emission is smaller with this technique compared to broadcasting. The average NH₃ loss was 50% of applied NH₄⁺ during warm/dry conditions and 10% during cold/wet conditions. The N₂O emission was always less than 1% of applied NH₄⁺. When the NH₃ emission decreased, the direct N₂O emission increased. However, when taking into account the indirect N₂O emission due to deposition of NH₃ outside the field, the spreading techniques all produced similar total N₂O emissions. The ammonia emission was not much lower for the band spreading technique compared to broadcasting, when compared on seven occasions.     

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.     

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.     

Mineralization of Nitrogen and N2O Production Potentials in Acid Forest Soils under Controlled Aerobic Conditions

Some acid surface mineral soils from different forest vegetations and sites in central Japan were taken during April and October in 2003 to study the net N mineralization and N₂O production potentials in the laboratory. Under the controlled aerobic conditions, 50 Pa C₂H₂ in the headspace can be used to study total gaseous-N losses during the aerobic mineralization and heterotrophic N₂O production in acid forest soils. The net N mineralization of these acid forest soils and N₂O-N production was variable with forest stands and with seasons, probably because of the quality of the litters and the variations of soil attributes. Three deciduous forest soils during two sampling reveal a higher potential for the total gaseous-N loss during the aerobic mineralization as compared with two coniferous forest soils. Heterotrophic nitrification among these acid forest soils accounted for the range from 37.0 to 76.3% of the total N₂O production under the experimental conditions, and was variable with forest stands and with seasons. Some factors regulating the net N mineralization and N₂O-N production were discussed in these acid forest soils.     

Mitigation of nitrous oxide emissions in spray-irrigated grazed grassland by treating the soil with dicyandiamide, a nitrification inhibitor

Abstract. Nitrous oxide (N₂O) from animal excreta in grazed pasture systems makes up a significant component (c. 10%) of New Zealand's total greenhouse gas inventory. We report an effective method to decrease N₂O emissions from animal urine patches by treating the soil with the nitrification inhibitor dicyandiamide (DCD), in a simulated grazed dairy pasture system under spray irrigation. The soil was a free-draining Lismore stony silt loam (Udic Haplustept loamy skeletal) and the pasture was a mixture of perennial ryegrass ( Lolium perenne ) and white clover ( Trifolium repens ). By treating the soil with DCD, N₂O emissions were decreased by 76% following urine application in the autumn, from 26.7 kg N₂O-N ha⁻¹ without DCD to an average of 6.4 kg N₂O-N ha⁻¹ with DCD over the 6-month experimental period. N₂O flux was decreased by 78% following urine application in the spring, from 18 kg N₂O-N ha⁻¹ without DCD to 3.9 kg N₂O-N ha⁻¹ with the application of DCD over the 3-month period. A single application of DCD immediately after urine was sufficient to effectively mitigate N₂O emissions from the urine. The results showed that repeated applications of DCD after urine application, or mixing DCD with urine, offered no advantage over a single application of DCD immediately after urine deposition.     

Nitrous oxide emissions from artificial urine patches applied to different N-fertilized swards and estimated annual N2O emissions for differently fertilized pastures in an upland location in Germany

Abstract. Artificial urine containing 20.2 g N per patch of 0.2 m² was applied in May and September to permanent grassland swards of a long‐term experiment in the western uplands of Germany (location Rengen/Eifel), which were fertilized with 0, 120, 240, 360 kg N ha^?1 yr^?1 given as calcium ammonium nitrate. The effect on N₂O fluxes measured regularly during a 357‐day period with the closed‐chamber technique were as follows. (1) N₂O emission varied widely among the fertilized control areas without urine, and when a threshold water‐filled pore space >60% was exceeded, the greater the topsoil nitrate content the greater the flux from the individual urine patches on the fertilized swards. (2) After urine application in May, 1.4–4.2% of the applied urine‐N was lost as N₂O from the fertilized swards; and after urine application in September, 0.3–0.9% of the applied urine‐N was lost. The primary influence on N₂O flux from urine patches was the date of simulated grazing, N‐fertilization rate being a secondary influence. (3) The large differences in N₂O emissions between unfertilized and fertilized swards after May‐applied urine contrasted with only small differences after urine applied in September, indicating an interaction between time of urine application and N‐fertilizer rate. (4) The estimated annual N₂O emissions were in the range 0.6–1.6 kg N₂O‐N per livestock unit, or 1.4, 3.6, 4.1 and 5.1 kg N₂O‐N ha^?1 from the 0–360 kg ha^?1 of fertilizer‐N. The study demonstrated that date of grazing and N‐fertilizer application could influence the N₂O emission from urine patches to such an extent that both factors should be considered in detailed large‐scale estimations of N₂O fluxes from grazed grassland.     

The use of a nitrification inhibitor, dicyandiamide (DCD), to decrease nitrate leaching and nitrous oxide emissions in a simulated grazed and irrigated grassland

Abstract. In grazed dairy pasture systems, a major source of NO₃^– leached and N₂O emitted is the N returned in the urine from the grazing animal. The objective of this study was to use lysimeters to measure directly the effectiveness of a nitrification inhibitor, dicyandiamide (DCD), in decreasing NO₃^– leaching and N₂O emissions from urine patches in a grazed dairy pasture under irrigation. The soil was a free‐draining Lismore stony silt loam (Udic Haplustept loamy skeletal) and the pasture was a mixture of perennial ryegrass (Lolium perenne) and white clover (Trifolium repens). The use of DCD decreased NO₃^–‐N leaching by 76% for the urine N applied in the autumn, and by 42% for urine N applied in the spring, giving an annual average reduction of 59%. This would reduce the NO₃^–‐N leaching loss in a grazed paddock from 118 to 46 kg N ha^–1 yr^–1. The NO₃^–‐N concentration in the drainage water would be reduced accordingly from 19.7 to 7.7 mg N L^–1, with the latter being below the drinking water guideline of 11.3 mg N L^–1. Total N₂O emissions following two urine applications were reduced from 46 kg N₂O‐N ha^–1 without DCD to 8.5 kg N₂O‐N with DCD, representing an 82% reduction. In addition to the environmental benefits, the use of DCD also increased herbage production by more than 30%, from 11 to 15 t ha^–1 yr^–1. The use of DCD therefore has the potential to make dairy farming more environmentally sustainable by reducing NO₃^– leaching and N₂O emissions.     

Effect of hydroquinone, dicyandiamide and encapsulated calcium carbide on urea N uptake by spring wheat, soil mineral N content and N2O emission

Abstract. At present about half of the N fertilizer used in China is as urea. However, recovery of urea N in crops is often limited to 30–40%. Application of urea in combination with hydroquinone plus dicyandiamide (U-HQ-DCD) gave an improved urea-N recovery and grain yield by spring wheat in a pot experiment. The apparent total urea-N recovery was 69% and 73% of this recovered N was found in the grain. The grain yield was 32% higher than in the treatment where urea was applied without inhibitors. The application of hydroquinone and dicyandiamide also resulted in a smaller soil nitrate content, which might restrict post-harvest leaching of N. Another beneficial effect of these inhibitors was that the N₂O emission from the soil—plant system was reduced by 35% compared to the treatment where only urea was applied. The use of urea in combination with hydroquinone plus encapsulated calcium carbide gave smaller beneficial effects.     

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.     

Nitrous oxide emissions from grassland in an intensive dairy farm in the Basque Country of Spain

Abstract. Intensively managed grasslands are potentially a large source of N₂O in the North Coast of Spain because of the large N input, the wet soil conditions and mild temperatures. To quantify the effect of fertilizer type and management practices carried out by farmers in this area, field N₂O losses were measured over a year using the closed chamber technique. Plots received two types of fertilizer: cattle slurry (536 kg N ha^–1) and calcium ammonium nitrate (140 kg N ha^–1). N₂O losses were less in the slurry treatment than after mineral fertilizer. This was probably due to high, short‐lived peaks of N₂O encountered immediately following mineral N addition. In contrast, the seasonal distribution of N₂O losses from the slurry amended plot was more uniform over the year. The greater N₂O losses in the mineral treatment might have been enhanced by the combined effect of mineral fertilizer and past organic residues present from previous organic amendments. Weak relationships were found between N₂O emission rates and soil nitrate, soil ammonium, soil water content and temperature. Better relationships were obtained in the mineral treatment than in the slurry plots, because of the wider range in soil mineral N. Water filled pore space (WFPS) was a key factor controlling N₂O emissions. In the > 90% WFPS range no relationships were found. The best regressions were found for the mineral treatment in the 40–65% WFPS range, 49% of the variance being explained by soil nitrate and ammonium content. In the 65–90% WFPS range, 43% of the variance was explained by nitrate only, but the inclusion of soil ammonium did not improve the model as it did in the 40–65% WFPS range. This fact indicates that nitrification is likely to be an important process involved in N₂O emissions at the 40–65% WFPS.     

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.     

Relationship between N2O and NO emission potentials and soil properties in Japanese forest soils

To determine the relationship between nitrous oxide (N₂O) and nitric oxide (NO) emission rates and soil properties in forest soils, N₂O and NO emission rates in soils were measured in incubation experiments under standardized temperature and water conditions (water content at a water-holding capacity of 60%) using soils packed into a cylindrical core, and variations in the soil properties were also determined. The N₂O emission rates from nitrification and from denitrification were determined separately using a nitrification inhibitor (10 Pa acetylene). Soil samples were taken from 25 forest stands in a central temperate area of Japan. The N₂O and NO emission rates were highly variable, even under the standardized temperature and water-holding capacity (60%) conditions. According to a partial least squared regression model analysis, the C:N ratio and pH strongly affected the N₂O emission rate, whereas     , water-soluble Al and the C:N ratio strongly affected the NO emission rate. The C:N ratio negatively affected the emission rate of both N oxide gases, suggesting that N mineralization is an important factor in the rates of N oxide gas emission. The acetylene inhibition experiment showed that N₂O emission from denitrification was positively affected by pH, water-filled pore space and filling density, and negatively affected by the C:N ratio, total carbon and total nitrogen.     

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.     

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.