The variation of greenhouse gas emissions from soils of various land-use/cover types in Jambi province,Indonesia

We measured fluxes of three greenhouse gases (N₂O, CO₂O and CH₄) from soils of six different land-use types at 27 temporary field sites in Jambi Province, Sumatra, Indonesia. Study sites included natural and logged-over forests; rubber plantation; oil palm plantation; cinnamon plantation; and grassland field. The ranges of N₂O, CO₂ and CH₄ fluxes were 0.13–55.8 gN m-2h-1; 1.38–5.16 g C m-2d-1; –1.27–1.18 mg C m-2d-1, respectively. The averages of N₂O, CO₂ and CH₄ fluxes at 27 sites were 9.4 gN m-2h-1,3.65 g C m-2d-1, –0.45 mg C m-2d-1, respectively. The values of CO₂ and CH₄ fluxes were comparable with those in the reports regarding other humid tropical forests, while the N₂O flux was relatively lower than those of previous reports. The N₂O fluxes in each soil type were correlated with the nitrification rates of soils of 0–5 cm depth. In Andisols, the ratio of the N₂O emission rate to the nitrification rate was possibly smaller than that of the other soil types. There was no clear relationship between N₂O flux and the soil water condition, such as water-filled pore space. Seventeen percent of CH₄ fluxes were positive; according to these positive fluxes, we did not find a good correlation between CH₄ uptake rate and soil properties. Although we performed a chronosequence analysis to produce some hypotheses about the effect of land-use change by a limited amount of sampling at one point in time, further tests are required for the future.     

Sources of nitrous oxide in soils

Research to identify sources of nitrous oxide (N₂O) in soils has indicated that most, if not all, of the N₂O evolved from soils is produced by biological processes and that little, if any, is produced by chemical processes such as chemodenitrification. Early workers assumed that denitrification was the only biological process responsible for N₂O production in soils and that essentially all of the N₂O evolved from soils was produced through reduction of nitrate by denitrifying microorganisms under anaerobic conditions. It is now well established, however, that nitrifying microorganisms contribute significantly to emissions of N₂O from soils and that most of the N₂O evolved from aerobic soils treated with ammonium or ammonium-yielding fertilizers such as urea is produced during oxidation of ammonium to nitrate by these microorganisms. Support for the conclusion that chemoautotrophic nitrifiers such as Nitrosomonas europaea contribute significantly to production of N₂O in soils treated with N fertilizers has been provided by studies showing that N₂O emissions from such soils can be greatly reduced through addition of nitrification inhibitors such as nitrapyrin, which retard oxidation of ammonium by chemoautotrophic nitrifiers but do not retard reduction of nitrate by denitrifying microorganisms. This revised version was published online in August 2006 with corrections to the Cover Date.     

Nitrous oxide (N2O) emissions from soils in warm climates

N₂O emission rates seem to be higher from soils in warm climates than from soils in temperate climates. Warm and moist conditions promote microbial processes that generate N₂O. Clearance of tropical forests enhances N₂O formation, but emission measurements from other agricultural operations in the tropics are few. Limiting fertilizer application to recommended rates applied at appropriate times and avoiding fallow land wherever practical serves to limit N₂O emissions. More specific advice for agriculture in warm climates requires further studies.     

Nitrous oxide emissions from agricultural soils

This paper addresses three topics related to N₂O emissions from agricultural soils. First, an assessment of the current knowledge of N₂O emissions from agricultural soils and the role of agricultural systems in the global N₂O are discussed. Secondly, a critique on the methodology presented in the OECD/OCDE (1991) program on national inventories of N₂O is presented. Finally, technical options for controlling N₂O emissions from agricultural fields are discussed.The amount of N₂O derived from nitrogen applied to agricultural soils from atmospheric deposition, mineral N fertilizer, animal wastes or biologically fixed N, is not accurately known. It is estimated that the world-wide N₂O emitteddirectly from agricultural fields as a result of the deposition of all the above nitrogen sources is 2–3 Tg N annually. This amounts to 20–30% of the total N₂O emitted annually from the earth's surface. An unknown, but probably significant, amount of N₂O is generated indirectly in on and off farm activities associated with food production and consumption.Management options to limitdirect N₂O emissions from N-fertilized soils should emphasize improving N-use efficiency. Such management options include managing irrigation frequency, timing and quantity; applying N only to meet crop demand through multiple applications during the growing season or by using controlled release fertilizers; applying sufficient N only to meet crop needs; or using nitrification inhibitors. Most of these options have not been field tested. Agricultural management practices may not appreciably affect indirect N₂O emissions.     

Contribution of nitrification and denitrification to N2O production in peat, clay and loamy sand soils under different soil moisture conditions

Agricultural soils are a significant source of nitrous oxide (N₂O). Since mitigation of greenhouse gas emissions is needed in all sectors of society, it is important to identify the processes producing N₂O and the factors affecting the production rates in agricultural soils. This study aimed to elucidate the N₂O production in peat, clay and loamy sand at four different soil moisture conditions (40, 60, 80 and 100% Water Filled Pore Space). The ace­tylene inhibition technique was used to evaluate the contribution of nitrification to N₂O production. Nitrous oxide production responded markedly to soil moisture in all three soils. The highest N₂O production, measured at the wettest soils (100% WFPS), was up to four orders of magnitude higher than that at the dry soils (40% WFPS). In dry conditions N₂O production decreased in the order of peat > clay > loamy sand, while in wet conditions the highest N₂O production was measured in loamy sand, then in peat, and the lowest in clay soils. Nitrification was the dominant N₂O producing process in all the soils at 60% WFPS. In the sandy soil 70% of the total N₂O production originated from nitrification, while in the peat soil most of the total N₂O production originated from denitrification. Data on processes producing N₂O in agricultural soils are needed to develop process-based models that could reduce the uncertainty of the emission estimates in greenhouse gas inventories.     

Measurement of nitrous oxide and di-nitrogen emissions from agricultural soils

Nitrous oxide can be produced during nitrification, denitrification, dissimilatory reduction of NO ₃ ^- to NH ₄ ⁺ and chemo-denitrification. Since soils are a mosaic of aerobic and anaerobic zones, it is likely that multiple processes are contributing simultaneously to N₂O production in a soil profile. The N₂O produced by all processes may mix to form one pool before being reduced to N₂ by denitrification. Reliable methods are needed for measuring the fluxes of N₂O and N₂ simultaneously from agricultural soils. The C₂H₂ inhibition and ¹⁵N gas-flux methods are suitable for use in undisturbed soils in the field. The main disadvantage of C₂H₂ is that as well as blocking N₂O reductase, it also blocks nitrification and dissimilatory reduction of NO ₃ ^- to NH ₄ ⁺ . Potentially the ¹⁵ N gas-flux method can give reliable measurements of the fluxes of N₂O and N₂ when all N transformation processes proceed naturally. The analysis of ¹⁵N in N₂ and N₂O is now fully automated by continuous-flow isotope-ratio mass spectrometry for 12-ml gas samples contained in septum-capped vials. Depending on the methodology, the limit of detection ranges from 4 to 11 g N ha^-1day^-1 for N₂ and 4 to 15 g N ha^-1day^-1 for N₂O. By measuring the ¹⁵N content and distribution of ¹⁵N atoms in the N₂O molecules, information can also be obtained to help diagnose the sources of N₂O and the processes producing it. Only a limited number of field studies have been done using the ¹⁵N gas-flux method on agricultural soils. The measured flux rates and mole fractions of N₂O have been highly variable. In rain-fed agricultural soils, soil temperature and water-filled pore space change with the weather and so are difficult to modify. Soil organic C, NO ₃ ^- and pH should be amenable to more control. The effect of organic C depends on the degree of anaerobiosis generated as a result of its metabolism. If conditions for denitrification are not limiting, split applications of organic C will produce more N₂O than a single application because of the time lag in the synthesis of N₂O reductase. Increasing the NO ₃ ^- concentration above the K _m value for NO ₃ ^- reductase, or decreasing soil pH from 7 to 5, will have little effect on denitrification rate but will increase the mole fraction of N₂O. The effect of NO ₃ ^- concentration on the mole fraction of N₂O is enhanced at low pH. Manipulating the interaction between NO ₃ ^- supply and soil pH offers the best hope for minimising N₂O and N₂ fluxes.     

Nitrous oxide emission from a rice paddy field in Japan

The flux of nitrous oxide (N₂O) from a rice paddy field to the atmosphere was measured at Ryuhgasaki experiment station in Ibaraki Prefecture of Japan by closed chamber method, from the summer of 1992 to the summer of 1993. During the rice-cultivated and flooding periods when methane (CH₄) was emitted, no emission or uptake of N₂O was measured because the flux values were below the detection limits. After the final water drainage for harvest in August or September, N₂O began to emit from the soil surface while the emission of CH₄ was stopped, and N₂O was emitted continually until the re-flooding day in the following spring. In the first few months after the final water drainage, the N₂O flux was in the range of 10–20 μgN/m²/hour, then in the latter several months during the cold season, the N₂O flux was less than 10 μgN/m²/hour. The vertical profiles of N₂O, CO₂ and CH₄ concentrations in the plowed layer of the soil down to a depth of 20 cm, were also measured six times in the fallow season. The maximum concentrations of N₂O and CO₂ were found in the plowed layer in the early period, and which demonstrates that most of the N₂O was produced in the plowed layer through nitrification, due to the decomposition of organic matter accumulated in the plowed layer during the rice-growing and water-flooding period. On the contrary, the vertical profiles in the cold season showed a gradual increase in the concentrations of N₂O and CO₂ in the plowed layer. It clearly indicates that a small amount of N₂O was emitted to the atmosphere by diffusion through the plowed layer from the sub-soil layer where a large source of N₂O was expected to exist. This revised version was published online in August 2006 with corrections to the Cover Date.     

Nitrite accumulation characteristics of high strength ammonia wastewater in an autotrophic nitrifying biofilm reactor

Selective nitrification was carried out to accumulate nitrite from high strength ammonia wastewater in an autotrophic nitrifying biofilm reactor. Nitrification efficiencies and nitrite accumulation characteristics were investigated at various operating conditions such as ammonium load, oxygen supply and free ammonia concentration. The biofilm reactor showed very stable nitrification efficiencies of more than 90% at up to 2 kg NH₄‐N m^?3 d^?1 and the nitrite content was maintained at around 95%. Inhibition by free ammonia on nitrite oxidizers seems to be the major factor for nitrite accumulation. Batch kinetic analyses of ammonium and nitrite oxidation showed that nitrite oxidation activity was selectively inhibited in the presence of free ammonia. However, the activity recovered quickly as the free ammonia concentration decreased below the threshold inhibition concentration. Examination of specific ammonia and nitrite oxidation activities and the most probable number indicated that the number of nitrite‐oxidizing microorganisms in the nitrite‐accumulating system was less than that in the normal nitrification system due to long‐term free ammonia inhibition of the nitrite oxidizers. The reduced population of nitrite oxidizers in the biofilm system was also responsible for the accumulation of nitrite in the biofilm reactor. © 2003 Society of Chemical Industry     

Nitrous oxide emissions for 6 years from a gray lowland soil cultivated with onions in Hokkaido, Japan

We studied nitrous oxide (N₂O) emissions every growing season (April to October) for 6 years (19952000), in a Gray Lowland soil cultivated with onions in central Hokkaido, Japan. Emission of N₂O from the onion field ranged from 0.00 to 1.86 mgN m^–2 h^–1. The seasonal pattern of N₂O emission was the same for 6 years. The largest N₂O emissions appeared near harvesting in August to October, and not, as might be expected, just after fertilization in May. The seasonal patterns of soil nitrate (NO₃ ^–) and, ammonium (NH₄ ⁺) levels and the ratio of N₂O to NO emission indicated that the main process of N₂O production after fertilization was nitrification, and the main process of N₂O production around harvest time was denitrification. N₂O emission was strongly influenced by the drying–wetting process of the soil, as well as by the high soil water content. The annual N₂O emission during the growing season ranged from 3.5 to 15.6 kgN ha^–1. The annual nitrogen loss by N₂O emission as a percentage of fertilizer-N ranged from 1.1 to 6.4%. About 70% of the annual N₂O emission occurred near harvesting in August to October, and less than 20% occurred just after fertilization in May to July. High N₂O fluxes around the harvesting stage and a high proportion of N₂O emission to total fertilizer-N appeared to be probably a characteristic of the study area located in central Hokkaido, Japan.     

Nitrification and denitrification derived N2O production from a grassland soil under application of DCD and Actilith F2

The relative contribution of nitrification and denitrification to N₂O production was investigated by means of soil incubations with acetylene in a mixed clover/ryegrass sown sward 5 days after application of a mineral fertiliser (calcium ammonium nitrate) or an organic one (cattle slurry) with and without the addition of the nitrification inhibitor dicyandiamide (DCD) and the commercial slurry additive Actilith-F2. At this time, maximum field N₂O emissions were taking place. N₂O production by the slurry amended soil was twice as high as that of the mineral amended one. N₂O came in a greater proportion from nitrification rather than from denitrification in the slurry treatment, while for the mineral fertilisation most N₂O came from denitrification. The addition of DCD to slurry produced a decrease in N₂O production both from nitrification and denitrification. No reduction in N₂O losses was observed from addition of DCD to the mineral fertilisation, although DCD resulted effective in reducing the nitrification rate by 53% both in the slurry and the mineral fertilisation. Actilith F2 induced a high nitrification rate and N₂O production from denitrification was reduced while that from nitrification was not. This revised version was published online in August 2006 with corrections to the Cover Date.     

Methane and Nitrous Oxide Emissions from Rice Field and Related Microorganism in Black Soil, Northeastern China

Methane (CH₄) and nitrous oxide (N₂O) emissions from rice field in black soil were measured in situ by using static chamber techniques during crop growth season in 2001. The experiment fields were divided into three plots for three different treatments, one with continuous flooded and applying urea (CU), one with continuous flooded and applying slow-releasing urea (CS), and one with intermittent irrigation and applying urea (IU). Under the same fertilization application, compared with continuous flooded, intermittent irrigation can significantly reduce CH₄ emission and increase N₂O emission. But, integrated global warming potentials (GWP_S) of CH₄ and N₂O emission were reduced greatly, while rice yield was not affected. So, the intermittent irrigation is an effective measure to reduce greenhouse gas emissions from paddy fields. The amount of CH₄ emission during rice-growing season for the three treatments was all much lower than that from any other region in China. There was a trade-off relationship between CH₄ and N₂O emissions. We also measured the numbers of methanogens, methanotrophs, nitrifiers and denitrifers from rice field at various growth stages in 2001. Bacteria populations were estimated by the most probable number (MPN) method. Regression analyses show CH₄ emissions were closely related to methanogens population for all the three treatments. There was a positive correlation between denitrifiers population level and N₂O emission in the treatment of IU.     

Fluxes of NO and N2O from temperate forest soils: impact of forest type, N deposition and of liming on the NO and N2O emissions

Annual cycles of NO, NO₂ and N₂O emission rates from soil were determined with high temporal resolution at a spruce (control and limed plot) and beech forest site (Höglwald) in Southern Germany (Bavaria) by use of fully automated measuring systems. The fully automated measuring system used for the determination of NO and NO₂ flux rates is described in detail. In addition, NO, NO₂ and N₂O emission rates from soils of different pine forest ecosystems of Northeastern Germany (Brandenburg) were determined during 2 measuring campaigns in 1995. Mean monthly NO and N₂O emission rates (July 1994–June 1995) of the untreated spruce plot at the Höglwald site were in the range of 20–130 µg NO-N m^-2 h^-1 and 3.5–16.4 µg N₂O-N m^-2 h^-1, respectively. Generally, NO emission exceeded N₂O emission. Liming of a spruce plot resulted in a reduction of NO emission rates (monthly means: 15–140 µg NO-N m^-2 h^-1) by 25-30% as compared to the control spruce plot. On the other hand, liming of a spruce plot significantly enhanced over the entire observation period N₂O emission rates (monthly means: 6.2–22.1 µg N₂O-N m^-2 h^-1). Contrary to the spruce stand, mean monthly N₂O emission rates from soil of the beech plot (range: 7.9–102 µg N₂O-N m^-2 h^-1) were generally significantly higher than NO emission rates (range: 6.1–47.0 µg NO-N m^-2 h^-1). Results obtained from measuring campaigns in three different pine forest ecosystems revealed mean N₂O emission rates between 6.0 and 53.0 µg N₂O-N m^-2 h^-1 and mean NO emission rates between 2.6 and 31.1 µg NO-N m^-2 h^-1. The NO and N₂O flux rates reported here for the different measuring sites are high compared to other reported fluxes from temperate forests. Ratios of NO/N₂O emission rates were >> 1 for the spruce control and limed plot of the Höglwald site and << 1 for the beech plot. The pine forest ecosystems showed ratios of NO/N₂O emission rates of 0.9 ± 0.4. These results indicate a strong differentiating impact of tree species on the ratio of NO to N₂O emitted from soil.     

Effects of free ammonia and dissolved oxygen on nitrification and nitrite accumulation in a biofilm airlift reactor

The purpose of this research is to find out the effects of free ammonia concentration and dissolved oxygen on nitrification and nitrite accumulation in a biofilm airlift reactor. Free ammonia seriously inhibited the activity of nitrite oxidizers at the concentration higher than 0.1 mg NH₃-N/L and it was very effective for nitrite accumulation. Dissolved oxygen limitation in the biofilm also caused nitrite accumulation. Long term inhibition decreased the growth rate for nitrite oxidizers, and ammonia oxidizers were the dominant nitrifiers in the wastewater nitrification. Selective accumulation of ammonia oxidizers in the biofilm could be another reason for nitrite accumulation. Free ammonia inhibited nitrite oxidizers immediately, and adaptation to free ammonia was not observed. Therefore, the optimum control of free ammonia and dissolved oxygen concentration is critical for nitrite accumulation and the strategy can be used for selective accumulation of ammonia oxidizers in a bioreactor system.     

Nitrous oxide emissions from fertilized upland fields in Thailand

Nitrous oxide (N₂O) emission from fertilized maize fields was measured using a closed chamber at four experimental sites in Thailand. The average measured N₂O flux from unfertilized plots through crop season was 4.16 ± 1.52, 5.05 ± 1.65, 5.25 ± 1.68 and 6.74 ± 2.95 g N₂O-N m^-2 h^-1, at Nakhon Sawan, Phra Phutthabat, Khon Kaen and Chiang Mai, respectively. Increased N₂O emissions by the application of nitrogen fertilizer were 0.22–0.44, 0.19–0.38%, 0.12–0.24 and 0.08–0.15% of the applied N, respectively. Compared to other data, N₂O emission rate to applied nitrogen was not significantly different between the data of Thailand and the Temperate Zone.     

Impact of mineral N fertilizer application rates on N2O emissions from arable soils under winter wheat

Nitrogen fertilizers are a major source of nitrous oxide (N₂O) emissions from arable soils. The relationship between nitrogen application rates and N₂O emissions was evaluated during the growth period of winter wheat (~140 days) at six field sites in north-western Germany. Nitrogen was applied as calcium–ammonium–nitrate, with application rates ranging between 0 and 400 kg N ha^?1. One trial was conducted in 2010, three trials in 2011 and two trials in 2012. Additionally, post-harvest N₂O emissions were evaluated at two field sites during autumn and winter (2012–2013). The emission factors (during the growth period) varied between 0.10 and 0.37 %. Annual N₂O emissions ranged between 0.46 and 0.53 % and were consistently lower across all sites and years than to the IPCC Tier 1 default value (1.0 %). Across all sites and years, the relationship between N₂O and N application rate was best described by linear regression even if nitrogen amounts applied were higher than the nitrogen uptake of the crop. Additionally, annual N₂O emissions per unit of harvested wheat grain were calculated for two field sites to assess the environmental impact of wheat grain production. Yield-scaled N₂O emissions followed a hyperbolic function with a minimum of 177 and 191 g N₂O–N t grain yield^?1 at application rates of 127 and 150 kg N ha^?1, followed by an increase at higher N application rates. This relationship indicates that wheat crop fertilization does not necessarily harm the environment through N₂O emissions compared to zero fertilization. Thus, improving nitrogen use efficiency may be the best management practice for mitigating yield-scaled N₂O emissions.     

Temporal and Spatial Variations in N2O Emissions from a Chinese Cabbage Field as a Function of Type of Fertilizer and Application

We conducted a field experiment in an Andosol near Tsukuba (Japan) to study the effects of the type of nitrogen fertilizer on nitrous oxide (N₂O) emissions and on nitrogen uptake by Chinese cabbage (Brassica campestris L.). We used four treatments: fertilizer containing no nitrogen (CONT), broadcast application of urea (BR-U), band application of urea (B-U), and band application of controlled-release urea (B-CU). The application rate was 250 kg N ha⁻¹, a conventional rate in the region. We measured N₂O flux two or three times a week during the 82-day growth period, then divided the cumulative emissions into three stages: early (28 days), middle (27 days), and late (27 days). The temporal variation in N₂O emissions differed among the treatments. Broadcast urea application produced 70% of N₂O emissions during the early stage. N₂O emissions increased with increasing cabbage growth in the CONT treatment, indicating that plant growth accompanied by increasing root biomass could stimulate N₂O emissions from unfertilized soil. There were no differences in the patterns of temporal variation in N₂O flux between the two band applications (B-U and B-CU); N₂O emissions in the early and middle stages were 46 and 42%, respectively, for B-U, vs. 41 and 40% for B-CU. However, the overall N₂O emission was reduced by 40.5% in the B-CU treatment compared with the B-U treatment. N₂O emissions from the soils within fertilized bands were dramatically higher than those between the fertilized bands, and this trend continued until harvesting.     

Effect of changing groundwater levels caused by land-use changes on greenhouse gas fluxes from tropical peat lands

Monthly measurements of carbon dioxide (CO₂), methane (CH₄) and nitrous oxide (N₂O) fluxes in peat soils were carried out and compared with groundwater level over a year at four sites (drained forest, upland cassava,upland and lowland paddy fields) located in Jambi province, Indonesia. Fluxes from swamp forest soils were also measured once per year as the native state of this investigated area. Land-use change from drained forest to lowland paddy field significantly decreased the CO₂ (from 266 to 30 mg C m^–2 h^–1) and N₂O fluxes (from 25.4 to 3.8 g N m^–2 h^–1), but increased the CH₄ flux (from 0.1 to 4.2 mg C m^–2 h^–1) in the soils. Change from drained forest to cassava field significantly increased N₂O flux (from 25.4 to 62.2 g N m^–2 h^–1), but had no significant influence on CO₂ (from 266 to 200 mg C m^–2 h^–1) and CH₄ fluxes (from 0.1 to 0.3 mg C m^–2 h^–1) in the soils. Averaged CO₂ fluxes in the swamp forests (94 mg C m^–2 h^–1) were estimated to be one-third of that in the drained forest. Groundwater levels of drained forest and upland crop fields had been lowered by drainage ditches while swamp forest and lowland paddy field were flooded, although groundwater levels were also affected by precipitation. Groundwater levels were negatively related to CO₂ flux but positively related to CH₄ flux at all investigation sites. The peak of the N₂O flux was observed at –20 cm of groundwater level. Lowering the groundwater level by 10 cm from the soil surface resulted in a 50 increase in CO₂ emission (from 109.1 to 162.4 mg C m^–2 h^–1) and a 25% decrease in CH₄ emission (from 0.440 to 0.325 mg C m^–2 h^–1) in this study. These results suggest that lowering of groundwater level by the drainage ditches in the peat lands contributes to global warming and devastation of fields. Swamp forest was probably the best land-use management in peat lands to suppress the carbon loss and greenhouse gas emission. Lowland paddy field was a better agricultural system in the peat lands in terms of C sequestration and greenhouse gas emission. Carbon loss from lowland paddy field was one-eighth of that of the other upland crop systems, although the Global Warming Potential was almost the same level as that of the other upland crop systems because of CH₄ emission through rice plants.     

Seasonal N<Subscript>2</Subscript>O emissions respond differently to environmental and microbial factors after fertilization in wheat–maize agroecosystem

Biogeochemical processes regulating cropland soil nitrous oxide (N₂O) emissions are complex, and the controlling factors need to be better understood, especially for seasonal variation after fertilization. Seasonal patterns of N₂O emissions and abundances of archaeal ammonia monooxygenase (amoA), bacterial amoA, nitrate reductase (narG), nitrite reductase (nirS/nirK), and nitrous oxide reductase (nosZ) genes in long-term fertilized wheat–maize soils have been studied to understand the roles of microbes in N₂O emissions. The results showed that fertilization greatly stimulated N₂O emission with higher values in pig manure-treated soil (OM, 2.88 kg N ha^?1 year^?1) than in straw-returned (CRNPK, 0.79 kg N ha^?1 year^?1) and mineral fertilizer-treated (NPK, 0.90 kg N ha^?1 year^?1) soils. Most (52.2–88.9%) cumulative N₂O emissions occurred within 3 weeks after fertilization. Meanwhile, N₂O emissions within 3 weeks after fertilization showed a positive correlation with narG gene copy number and a negative correlation with soil NO₃^? contents. The abundances of narG and nosZ genes had larger direct effects (1.06) than ammonium oxidizers (0.42) on N₂O emissions according to partial least squares path modeling. Stepwise multiple regression also showed that log narG was a predictor variable for N₂O emissions. This study suggested that denitrification was the major process responsible for N₂O emissions within 3 weeks after fertilization. During the remaining period of crop growth, insufficient N substrate and low temperature became the primary limiting factors for N₂O emission according to the results of the regression models.     

Effect of chemical fertilizer form on N2O, NO and NO2 fluxes from Andisol field

N₂O, NO and NO₂ fluxes from an Andosol soil in Japan after fertilization were measured 6 times per day for 10 months from June 1997 to April 1998 with a fully automated flux monitoring system in lysimeters. Three nitrogen chemical fertilizers were applied to the soil–calcium nitrate (NI), controlled-release urea (CU), and controlled-release calcium nitrate (CN), and also no nitrogen fertilizer (NN). The total amount of nitrogen applied was 15 g N m^–2 in the first and the second cultivation period of Chinese vegetable. In the first measuremnt period of 89 days, the total N₂O emissions from NI, CN, CU, and NN were 18.4, 16.3, 48.7, and 9.60 mgN m^–2, respectively. The total NO emissions from NI, CN, CU, and NN were 48.4, 33.7, 149, and 13.7 mgN m^–2, respectively. In the second measurement period of 53 days, the total N₂O emissions from NI, CN, and CU were 9.66, 7.23, and 20.6 mgN m^–2, respectively. The total NO emissions from NI, CN, and CU were 24.7, 2.60 and 34.2 mgN m^–2, respectively. The total N₂O emission from CU was significantly higher than CN. In the third cultivation period, all plots were applied with 10 g N m^–2 of ammonium phosphate (AP) and winter barley was cultivated. In the third measurement period of 155 days, the total N₂O and NO emissions were 9.02 mgN m^–2 and 10.2 mgN m^–2, respectively. N₂O and NO peaks were observed just after the fertilization for 30 days and 15 days, respectively. N₂O, NO and NO₂ fluxes for the year were estimated to be 38.6 81.5, 48.2 181, and –24.8 to –39.3 mgN m^–2, respectively. NO₂ was absorbed in all the plots, and a negative correlation was found between NO₂ flux and the NO₂ concentration just after the chamber closed. NO was absorbed in the winter period, and a negative correlation was found between NO flux and the NO concentration just after the chamber closed. A diurnal pattern was observed in N₂O and NO fluxes in the summer, similar to air and soil temperature. We could find a negative relationship between flux ratio of NO-N to N₂O-N and water-filled pore space (WFPS), and a positive relationship between NO-N and N₂O-N fluxes and temperature. Q₁₀ values were 3.1 for N₂O and 8.7 for NO between 530 °C.     

Nitrite in soils: accumulation and role in the formation of gaseous N compounds

Nitrite is an intermediary compound formed during nitrification as well as denitrifiication. It occasionally accumulates in soils and drainage water. The nitrite can then undergo transformations to gaseous nitrogen compounds such as NO and NO₂. Soil pH controls the abiotic nitrite decomposition to a large extent. Under acidic conditions(pH <5.5), nitrous acid spontaneously decomposes preferentially to NO and NO₂. Nitrite also undergoes reactions with metallic cations (especially ferrous iron) and with organic matter. As a result of these reactions gaseous compounds such as NO, NO₂, N₂O and CH₃ONO can be formed. Through reaction of nitrite with phenolic compounds nitroand nitrosocompounds can be formed, building up organic N. With normal agricultural practices on slightly acidic soils, the nitrite instability usually does not lead to economically important N losses from soils. However, the compounds formed through its degradation or interaction with other soil constituents are linked to environmental problems such as tropospheric ozone formation, acid rain, the greenhouse effect and the destruction of the stratospheric ozone.