Gaseous nitrogen losses from soil under Sitka spruce following the application of fertilizer 15N urea

Gaseous N loss, through denitrification and NH₃⁻volatilization, was monitored throughout the growing season after spring application of ¹⁵N labelled urea fertilizer to peaty gley soils supporting N-deficient Sitka spruce. From the ¹⁵N data, it was calculated that only about 0.28% of applied N was lost through NH₃-volatilization, almost all within the first few days after fertilizer application. Approximately 0.05% of applied N was calculated to be lost through denitrification. Denitrification decreased slowly over a 4-month period after fertilizer application. Rates of NH₃-volatilization correlated with available NH₄⁺ in the litter layer, while for the early part of the study when N-losses were highest, denitrification rates correlated with available NO₃⁻ in the litter layer. Observations of gaseous N-loss are also discussed in relation to data from lysimetry, changes in soil pH, and the soil moisture regime.     

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.     

Inhibition of nitrate accumulation in tropical grassland soils: effect of nitrogen fertilization and soil disturbance

In acid soils in the Eastern Plains of Colombia, forage grasses planted on land prepared before the previous dry season produced 40–50% more dry matter than when land was prepared immediately before planting. Virtually no NO₃⁻ accumulated in surface (0–10 cm) soil from three native undisturbed savanna sites. Where land was ploughed before the dry season, NO₃⁻ levels increased gradually after a 2–3 month lag, and dropped at the beginning of the rains. In samples incubated for 4 weeks, more NO₃⁻ accumulated in the wet than the dry season. A similar 2–3-month lag occurred when land was ploughed after the dry season. NH₄⁺ levels were higher in ploughed than savanna soils, and rose in all soils at the beginning of the rains. More NO₃⁻ and NH₄⁺ accumulated on incubation in pots than in soil cores. Forage grasses inhibited NO₃⁻ accumulation in the soil, relative to plant-free plots, and legumes stimulated it. N fertilization overcame this inhibition except in the case of Brachiaria humidicola .     

Nitrous oxide emissions after application of inorganic fertilizer and incorporation of green manure residues

Abstract. Emissions of N₂O were measured after application of NH₄NO₃ fertilizer and incorporation of winter wheat and rye green manures in two field experiments in southeast England. Incorporation of green manure alone resulted in temporary immobilization of soil N, small N₂O emissions and also low availability of N for the following crop. Emissions were increased after application of inorganic fertilizer, and were further increased from integrated management treatments whereby green manure residues were incorporated after fertilizer application. The highest emission was from the incorporated winter wheat green manure plus fertilizer treatment, with 1.5 kg N₂O-N ha⁻¹ (0.6% of N applied) being emitted over the first 55 days after incorporation. This high emission was attributed to the supply of C in the residues providing the energy for denitrification in the presence of large amounts of mineral N and the creation of anaerobic microsites during microbial respiration.     

Denitrification in drained and undrained arable clay soil

Emissions of nitrous oxide (N₂O) and nitrogen gas (N₂) from denitrification were measured using the acetylene inhibition method on drained and undrained clay soil during November 1980-June 1981. Drainage limited denitrification to about 65% of losses from undrained soil. Emissions from the undrained soil were in the range 1 to 12 g N ha^–1 h^–1 while those from the drained soil ranged from 0.5 to 6 g N ha^–1 h^–1 giving estimated total losses (N₂O + N₂) of 14 and 9 kgN ha^–1.
Drainage also changed the fraction of nitrous oxide in the total denitrification product. During December, emissions from the drained soil (1.8±0.6 gN ha^–1 h^–1) were composed entirely of nitrous oxide, but losses from the undrained soil (2.7 ± 1.1 g N ha^–1 h^–1) were almost entirely in the form of nitrogen gas (the fraction of N₂O in the total loss was 0.02). In February denitrification declined in colder conditions and the emission of nitrous oxide from drained soil declined relative to nitrogen gas so that the fraction of N₂O was 0.03 on both drainage treatments. The delayed onset of N₂O reduction in the drained soil was related to oxygen and nitrate concentrations. Fertilizer applications in the spring gave rise to maximum rates of emission (5–12g N ha^–1 h^–1) with the balance shifting towards nitrous oxide production, so that the fraction of N₂O was 0.2–0.8 in April and May.     

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.     

Characterization of Treatment Processes and Mechanisms of COD, Phosphorus and Nitrogen Removal in a Multi-Soil-Layering System

Characteristics of the treatment processes inside a MSL system were investigated by using a laboratory-scale MSL system, which was set up in a D 10 × W 50 × H 73 cm acrylic box enclosing "soil mixture blocks" alternating with permeable zeolite layers. For the study of the treatment processes inside the system, wastewater, with mean concentrations (mg L⁻¹) of COD: 70, T-N: 12, T-P: 0.9, was introduced into the system at a loading rate of 1,000 L m⁻² d⁻¹. Treatment processes in the MSL system were different for the COD, P and N pollutants. Eighty percent of COD was removed in the 1st soil layer among the 6 layers, and the removal rate increased as water moved down and finally reached 90% in the last layer of the system. Phosphorus concentration was lower under the soil mixture layers than under the permeable layers, presumably because P was adsorbed mainly by soil and mixed iron particles. The P concentration in water gradually decreased in the lower layers of the system. The concentration of PO₄^3--P was generally lower in the aerated MSL system than in the non-aerated one. NH₄⁺-N was adsorbed and nitrified in the upper part of the system. The NO₃⁻-N concentration was lower in water under the soil mixture layers than under the permeable layers, indicating that denitrification mainly occurred in the soil mixture layers.     

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.     

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.     

Effect of Inorganic N Composition of Fertilizers on Nitrous Oxide Emission Associated with Nitrification and Denitrification

We studied the effect of repeated application (once every 2 d) of a fertilizer solution with different ratios of NH₄ ⁺ - and NO₃ ^?-N on N₂O emission from soil. After the excess fertilizer solution was drained from soil, the water content of soil was adjusted to 50% of the maximum water-holding capacity by suction at 6 × 10³ Pa. Repeated application of NH₄ ⁺- rich fertilizer solution stimulated nitrification in soil more than NO₃ ^?-rich fertilizer. Although the evolution of N₂O through nitrifier denitrification tended to increase with the repeated addition of a fertilizer solution rich in NH₄ ⁺ rather than in NO₃ ^?, the contribution of nitrifier denitrification remained at levels of 20 to 36% of the total emission regardless of the inorganic N composition. The total emission of N₂O also tended to increase with the application of NH₄ ⁺- rather than NO₃ ^?-rich fertilizer. It was suggested that the coupled process of nitrification and denitrification at micro-aerobic sites became important when fertilizer rich in NH₄ ⁺ was applied to soil under relatively aerobic conditions.     

An introduction to the global nitrogen cycle

Abstract. Current estimates are tabulated for the quantities of nitrogen circulating in the global nitrogen cycle. Five gases, NH₃, N₂O, NO, NO₂ and N₂, dominate the movement of nitrogen between the earth's surface and the atmosphere. The input of combined nitrogen to the land surface of the earth is tentatively estimated at 290 million tonnes per year, a total which includes 74 million tonnes from fertilizers. Known outputs from land (as gaseous NH₃, N₂O and NO_X, and as inorganic nitrogen carried to the sea by rivers) are much less, totalling 130 million tonnes per year. Emissions of N₂ gas probably account for most of the difference. There has been an increase in the use of nitrogen of about 5% per year over the last ten years. The demand for fertilizer nitrogen is likely to continue to grow if the population of the world continues to increase.     

Spatial variations in nitrous oxide and nitric oxide emission potential on a slope of Japanese cedar (Cryptomeria japonica) forest

To quantify the spatial variation and spatial structure of nitrous oxide (N₂O) and nitric oxide (NO) emission from forest soils, we measured N₂O and NO emission rates from surface soil cores taken at 1 m intervals on a cross-line transect (65 m × 20 m) on a slope of Japanese cedar ( Cryptomeria japonica ) forest in a temperate region of central Japan and analyzed the spatial dependency of N oxide gas emissions using geostatistics. We divided N₂O emission into N₂O from denitrification and N₂O from nitrification using the acetylene inhibition method. According to the geostatistical analysis, N₂O emission rates on the slope had large spatial variation and weak spatial dependency. This weak spatial dependency was caused by the inordinately high N₂O emissions on the slope, which were derived mainly from denitrification. In contrast, NO emission rate on the slope had large spatial variation, but strong spatial dependency and a distinct spatial distribution related to slope position, that is, high in the middle of the slope and low in the shoulder and the foot of the slope. The CN ratio and water-filled pore space were the dominant factors controlling NO emission rate on a slope. Our results suggest that spatial information about topographic factors helps to improve the estimation of both N₂O emission and NO emission from forest soils.     

Carbon and nitrogen mineralization of sewage sludge compost in soils with a different initial pH

Soil properties may affect the decomposition of added organic materials and inorganic nitrogen (N) production in agricultural soils. Three soils, Potu (Pu), Sankengtzu (Sk) and Erhlin (Eh) soils, mixed with sewage sludge compost (SSC) at application rates of 0 (control), 25, 75 and 150 Mg ha⁻¹ were selected from Taiwan for incubation for 112 days. The aim of the present study was to examine the effects of SSC application rates on the carbon decomposition rate, N transformation and pH changes in three soils with different initial soil pH values (4.8–7.7). The results indicated that the highest peaks of the CO₂ evolution rate occurred after 3 days of incubation, for all treatments. The Pu soil (pH 4.8) had a relatively low rate of CO₂ evolution, total amounts of CO₂ evolution and percentage of added organic C loss, all of which resulted from inhibition of microbial activity under low pH. For the Pu and Sk soils, the concentration of NH₄⁺-N reached its peak after 7–14 days of incubation, which indicated that ammonification might have occurred in the two soils with low initial pH values. NO₃⁻-N rapidly accumulated in the first 7 days of incubation in the Eh soil (pH 7.7). The direction and extent of the soil pH changes were influenced by the N in the SSC and the initial soil pH. Ammonification of organic N in the SSC caused the soil pH to increase, whereas nitrification of mineralized N caused the soil pH to decline. Consequently, the initial soil pH greatly affected the rate of carbon decomposition, ammonification and nitrification of SSC.     

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.     

Methane consumption in a frequently nitrogen-fertilized and limed spruce forest soil after clear-cutting

Abstract. The effects of especially frequent nitrogen (N) additions (from 1959 to 1986, totalling 860 kg N ha⁻¹) and liming (in 1958 and 1980, totalling 6000 kg CaCO₃ ha⁻¹) on CH₄ uptake by a boreal forest soil were studied in a stand of Norway spruce. Except for a forested reference plot, the stand was clear-cut in January 1993 and the following year one-half of each clear-cut plot was prepared by mounding. Fluxes of CH₄ were measured with static chambers in the autumn before clear-cutting and during the following four summers. The average CH₄ uptake during 1993–96 in the forested reference plot was 82 μg CH₄ m⁻² h⁻¹(ranging from 10 to 147 units). In the first summer after clear-cutting, the cleared plot showed 42% lower CH₄ uptake rate than the forested reference plot, but thereafter the difference became less pronounced. The short-term decrease in CH₄ consumption after clear-cutting was associated with increases in soil NH₄⁺ and NO₃⁻concentrations. Mounding tended at first to stimulate CH₄ uptake but later to inhibit it. Neither liming nor N-fertilization had significant effects on CH₄ consumption. Our results suggest that over the long term, in N-limited upland boreal forest soils, N addition does not decrease CH₄ uptake by the soil.     

The effect of soil texture and soil drainage on emissions of nitric oxide and nitrous oxide

Abstract. Agricultural soils are important sources of the tropospheric ozone precursor NO and the greenhouse gas N₂O. Emissions are controlled primarily by parameters that vary the soil mineral N supply, temperature and soil aeration. In this field experiment, the importance of soil physical properties on emissions of NO and N₂O are identified. Fluxes were measured from 13 soils which belonged to 11 different soil series, ranging from poorly drained silty clay loams to freely drained sandy loams. All soils were under the same soil management regime and crop type (winter barley) and in the same maritime climate zone. Despite this, emissions of NO and N₂O ranged over two orders of magnitude on all three measurement occasions, in spring before and after fertilizer application, and in autumn after harvest. NO emissions ranged from 0.3 to 215 μg NO-N m^–2 h^–1, with maximum emissions always from the most sandy, freely drained soil. Nitrous oxide emissions ranged from 0 to 193 μg N₂O-N m^–2 h^–1. Seasonal shifts in soil aeration caused maximum N₂O emissions to switch from freely drained sandy soils in spring to imperfectly drained soils with high clay contents in autumn. Although effects of soil type on emissions were not consistent, N₂O emission was best related to a combination of bulk density and clay content and the NO/N₂O ratio decreased logarithmically with increasing water filled pore space.     

Mitigation of greenhouse gas emissions from soil under silage production by use of organic manures or slow-release fertilizer

Abstract. Grassland is a major source of nitrous oxide (N₂O) and methane (CH₄) emissions in the UK, resulting from high rates of fertilizer application. We studied the effects of substituting mineral fertilizer by organic manures and a slow-release fertilizer in silage grass production on greenhouse gas emissions and soil mineral N content in a three-year field experiment. The organic manures investigated were sewage sludge pellets and composted sewage sludge (dry materials), and digested sewage sludge and cattle slurry (liquid materials). The organic manures produced N₂O and carbon dioxide (CO₂) consistently from time of application up to harvest. However, they mitigated N₂O emissions by around 90% when aggregate emissions of 15.7 kg N ha⁻¹ from NPK fertilizer were caused by a flux of up to 4.9 kg N ha⁻¹ d⁻¹ during the first 4 days after heavy rainfall subsequent to the NPK fertilizer application. CH₄ was emitted only for 2 or 3 days after application of the liquid manures. CH₄ and CO₂ fluxes were not significantly mitigated. Composting and dried pellets were useful methods of conserving nutrients in organic wastes, enabling slow and sustained release of nitrogen. NPK slow-release fertilizer also maintained grass yields and was the most effective substitute for the conventional NPK fertilizer for mitigation of N₂O fluxes.     

Methane and nitrous oxide fluxes from a farmed Swedish Histosol

Fluxes of the greenhouse gases methane (CH₄) and nitrous oxide (N₂O) from histosolic soils (which account for approximately 10% of Swedish agricultural soils) supporting grassley and barley production in Sweden were measured over 3 years using static chambers. Emissions varied both over area and time. Methane was both produced and oxidized in the soil: fluxes were small, with an average emission of 0.12 g CH₄ m⁻² year⁻¹ at the grassley site and net uptake of −0.01 g CH₄ m⁻² year⁻¹ at the barley field. Methane emission was related to soil water, with more emission when wet. Nitrous oxide emissions varied, with peaks of emission after soil cultivation, ploughing and harrowing. On average, the grassley and barley field had emissions of 0.20 and 1.51 g N₂O m⁻² year⁻¹, respectively. We found no correlation between N₂O and soil factors, but the greatest N₂O emission was associated with the driest areas, with < 60% average water-filled pore space. We suggest that the best management option to mitigate emissions is to keep the soil moderately wet with permanent grass production, which restricts N₂O emissions whilst minimizing those of CH₄.     

Relationship between nitrifier and denitrifier community composition and abundance in predicting nitrous oxide emissions from ephemeral wetland soils

The link between differences in the community composition of nitrifiers and denitrifiers to differences in the emission of nitrous oxide (N₂O) from soils remains unclear. Nitrifier and denitrifier community composition, abundance and N₂O emission activity were determined for two common landscapes characteristic of the North American “prairie pothole region”: cultivated wetlands (CW) vs. uncultivated wetlands (UW). The hypotheses of this study were: (1) landscape selects for different nitrifier and denitrifier communities, (2) denitrification was the dominant N₂O emitting process, and (3) a relationship exists between nitrifier and denitrifier community composition, their abundance, and N₂O emission. Comparisons were made among soils from three CW and three UW at the St. Denis National Wildlife Area. Denaturing gradient gel electrophoresis was used to compare community composition, and quantitative polymerase chain reaction was used to estimate community size. Incubation experiments on re-packed soil cores with ¹⁵N-labeled nitrate were performed to assess the relative contributions of nitrification and denitrification to total N₂O emission. Results indicate: (1) nitrification was the primary source of N₂O emission, (2) cultivation increased nitrifier abundance but decreased nitrifier richness, (3) denitrifier abundance was not affected by cultivation but richness was increased by cultivation, and (4) differences in nitrifier and denitrifier communities composition and abundance between land-use and landform did not correspond to differences in N₂O emission.