Comparing measured and Expert-N predicted N2O emissions from conventional till and no till corn treatments

Agricultural soils are a major source of the greenhouse gas nitrous oxide (N₂O). Nitrous oxide emission models can be used to predict the effectiveness of N₂O mitigation strategies; however, these models require rigorous testing before they can be used with confidence. Expert-N, a modular process based N₂O emission model, was tested to determine its ability at predicting nitrogen (N) cycling in the soil–plant–atmosphere system under Canadian agroclimatic conditions. Ancillary data and N₂O emissions were collected/measured from a corn cultivated clay-loam soil that was under different tillage and red clover treatments. The treatments were conventional till (CT) with and without red clover (rc) underseeded in the previous year's wheat crop (CT-Crc and CT-C, respectively), and no till (NT) with and without red clover underseeded in the previous year's wheat crop (NT-Crc and NT-C, respectively). Expert-N provided good estimates of N₂O emissions, and predictions correlated well (positive) with the measured emissions (r ² 0.55–0.83). There was no statistically significant difference between measured and predicted daily emissions. The predicted emissions, integrated over the growing season (25 May–4 October, 1995), were 0.56, 0.57, 0.62, and 0.62 kg N₂O-N ha^–1 for CT-C, CT-Crc, NT-C, and NT-Crc, respectively. The measured emissions over the same period were 1.29, 1.07, 0.96, and 1.04 kg N₂O-N ha^–1 for CT-C, CT-Crc, NT-C, and NT-Crc, respectively. The modelled emissions underestimated the integrated measured emissions by 35–55%; however, the integrated measured emissions had an estimated uncertainty of ±35%. The model provided good predictions of the soil temperatures, moisture contents, and soil nitrate levels with no significant difference from the measured data. Correlations between modelled and measured values for these soil properties in the first 30 cm soil layer were positive and high with r ² 0.71–0.93.     

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.     

Measurement of nitrous oxide emissions from two rice-based cropping systems in China

A field experiment was conducted to investigate the effects of winter management and N fertilization on N₂O emission from a double rice-based cropping system. A rice field was either cropped with milk vetch (plot V) or left fallow (plot F) during the winter between rice crops. The milk vetch was incorporated in situ when the plot was prepared for rice transplanting. Then the plots V and F were divided into two sub-plots, which were then fertilized with 276 kg urea-N ha^–1 (referred to as plot VN and plot FN) or not fertilized (referred to as plot VU and plot FU). N₂O emission was measured periodically during the winter season and double rice growing seasons. The average N₂O flux was 11.0 and 18.1 g N m^–2 h^–1 for plot V and plot F, respectively, during winter season. During the early rice growing period, N₂O emission from plot VN averaged 167 g N m^–2 h^–1, which was eight- to fifteen-fold higher than that from the other three treatments (17.8, 21.0 and 10.8 g N m^–2 h^–1 for plots VU, FN, and FU, respectively). During the late rice growing period, the mean N₂O flux was 14.5, 11.1, 12.1 and 9.9 g N m^–2 h^–1 for plots VN, VU, FN and FU, respectively. The annual N₂O emission rates from green manure-double rice and fallow-double rice cropping systems were 3.6 kg N ha^–1 and 1.3 kg N ha^–1, respectively, with synthetic N fertilizer, and were 0.99 kg N ha^–1 and 1.12 kg N ha^–1, respectively, without synthetic N fertilizer. Generally, both green manure N and synthetic fertilizer N contribute to N₂O emission during double rice season.     

Nitrous oxide emissions from paddy soil in three rice-based cropping systems in China

Rice-flooding fallow, rice-wheat, and double rice-wheat systems were adopted in pot experiment in an annual rotation to investigate the effects of cropping system on N₂O emission from rice-based cropping systems. The annual N₂O emission from the rice-wheat and the double rice-wheat cropping systems were 4.3 kg N ha^–1 and 3.9 kg N ha^–1, respectively, higher than that from rice-flooding fallow cropping system, 1.4 kg N ha^–1. The average N₂O flux was 115 and 118 g N m^–2 h^–1 for rice season in rice-wheat system and early rice season in double rice-wheat system, respectively, 68.6 and 35.3 g N m^–2 h^–1 for the late rice season in double rice-wheat system and rice season in rice-flooding fallow, respectively, and only 3.1–5.3 g N m^–2 h^–1 for winter wheat or flooding fallow season. Temporal variations of N₂O emission during rice growing seasons differed and high N₂O emission occurred when soil conditions changed from upland crop to flooded rice.     

Nitrous oxide emission from temperate meadow grassland and emission estimation for temperate grassland of China

Nitrous oxide emission from temperate meadow grassland was measured using a closed chamber method at two experimental sites in China. In the four-month measurement period, the N₂O fluxes in mown meadow grasslands of the Songnen Plain and of the Kerqin Steppe were on average 41.1 and 7.9 g N₂O-N m^–2 h^–1, respectively. Considering the influence of grassland type and degradation extent, an empirical formula was constructed, with which the annual N₂O emission from temperate grassland of China was estimated as 40.4 Gg N. Meadow grassland, accounting for 14.0% of the total grassland area, contributed 28.4% of the total N₂O emission.     

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.     

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.     

Spatial patterns of greenhouse gas emission in a tropical rainforest in Indonesia

Spatial patterns of CO₂, CH₄, and N₂O flux were analyzed in the soil of a primary forest in Sumatra, Indonesia. The fluxes were measured at 3-m intervals on a sampling grid of 8 rows by 10 columns, with fluxes found to be below the minimum detection level at 12 points for CH₄ and 29 points for N₂O. All three gas fluxes distributed log-normally. The means and standard deviations of CO₂ and CH₄ fluxes calculated by the maximum likelihood method were 3.68 ± 1.32 g C m^–2 d^–1 and 0.79 ± 0.60 mg C m^–2 d^–1, respectively. The mean and standard deviation of N₂O fluxes using a maximum likelihood estimator for the censored data set was 2.99 ± 3.26 g N m^–2 h^–1. The spatial dependency of CH₄ fluxes was not detected in 3-m intervals, while weak spatial dependency was observed in CO₂ and N₂O fluxes. The coefficients of variation of CH₄ and N₂O were higher than that of CO₂. Some hot spots where high levels of CH₄ and N₂O were generated in the studied field may increase the variability of these gases. The resulting patterns of variability suggest that sampling distances of >10 m and > 20 m are required to obtain statistically independent samples for CO₂ and N₂O flux in the studied field, respectively. But because of weak or no spatial dependency of each flux, a sampling distance of more than 10 m intervals is enough to prevent a significant problem of autocorrelation for each flux measurement.     

Nitrous oxide emission as affected by liming an acidic mineral soil used for arable agriculture

The effect of liming an acidic mineral soil (Dystric Nitosol from southern China), used for arable agriculture, on N₂O emission was studied in an incubation experiment. After the soil pH had been raised from pH 4.4 to 5.2, 6.7 and 8.1, soil samples were either amended with NH₄ ⁺ and incubated aerobically, favoring nitrification or, after application of NO₃ ^–, the incubation took place under anaerobic conditions, favoring denitrification. Gas sampling for N₂O determination and soil analyses were performed at regular intervals up to 13 days. Under nitrification conditions only small N₂O emission rates were observed (max. 6 g N kg^–1 d^–1) with significant differences between high and low pH values during the first 2 days of incubation. The nitrifying activity was low, even with high pH, and this, together with good aeration conditions, could partly explain the small N₂O evolution. During denitrification, however, cumulative N₂O emissions reached much higher values (1600 g N kg^–1 in comparison to 40 g N kg^–1 under nitrification conditions). N₂O emission during denitrification was significantly enhanced by increasing soil pH. Under alkaline conditions (pH 8.1) a large nitrite accumulation occurred, which was in line with the highest nitrate reductase activity determined in this treatment. The limited availability of organic carbon is probably the main reason for the absence of further reduction of NO₂ ^– to N₂O or N₂. At pH 6.7 the total N₂O emission was slightly higher than at pH 8.1, although the start of pronounced emissions was retarded and only small amounts of NO₂ ^– accumulated. Acid soil conditions caused either negligible (pH 4.4) or only small (pH 5.2) N₂O emissions. It can be concluded that these kinds of soil, used alternatively for production of upland crops or paddy rice, are prone to high N₂O emissions after flooding, particularly under neutral to alkaline conditions. In order to avoid major N₂O evolution and accumulation of nitrite, which can be leached into groundwater, the pH should not be raised to values above 5.5–6.     

Effects of type and amount of applied nitrogen fertilizer on nitrous oxide fluxes from intensively managed grassland

Five field experiments and one greenhouse experiment were carried out to assess the effects of nitrogen (N) fertilizer type and the amount of applied N fertilizer on nitrous oxide (N₂O) emission from grassland. During cold and dry conditions in early spring, emission of N₂O from both ammonium (NH ₄ ⁺ ) and nitrate (NO ₃ ^– ) containing fertilizers applied to a clay soil were relatively small, i.e. less than 0.1% of the N applied. Emission of N₂O and total denitrification losses from NO ₃ ^– containing fertilizers were large after application to a poorly drained sand soil during a wet spring. A total of 5–12% and 8–14% of the applied N was lost as N₂O and via denitrification, respectively. Emissions of N₂O and total denitrification losses from NH ₄ ⁺ fertilizers and cattle slurry were less than 2% of the N applied. Addition of the nitrification inhibitor dicyandiamide (DCD) reduced N₂O fluxes from ammonium sulphate (AS). However, the effect of DCD to reduce total N₂O emission from AS was much smaller than the effect of using NH ₄ ⁺ fertilizer instead of NO ₃ ^– fertilizer, during wet conditions. The greenhouse study showed that a high groundwater level favors production of N₂O from NO ₃ ^– fertilizers but not from NH ₄ ⁺ fertilizers. Inereasing calcium ammonium nitrate (CAN) application increased the emitted N₂O on grassland from 0.6% of the fertilizer application rate for a dressing of 50 kg N ha^–1 to 3.1% for a dressing of 300 kg N ha^–1. In another experiment, N₂O emission increased proportionally with increasing N rate. The results indicate that there is scope for reducing N₂O emission from grasslands by choosing the N fertilizer type depending on the soil moisture status. Avoiding excessive N application rates may also minimize N₂O emission from intensively managed grasslands.     

Nitrous oxide formation potential of various humid tropic soils of Malaysia: A laboratory study

Nitrous oxide (N₂O) is formed mainly during nitrification and denitrification. Inherent soil properties strongly influence the magnitude of N₂O formation and vary with soil types. A laboratory study was carried out using eight humid tropic soils of Malaysia to monitor NH₄ ⁺ and NO₃ ^– dynamics and N₂O production. The soils were treated with NH₄NO₃ (100 mg N kg^–1 soil) and incubated for 40 days at 60% water-filled pore space. The NH₄ ⁺ accumulation was predominant in the acid soils studied and NO₃ ^– accumulation/disappearance was either small or stable. However, the Munchong soil depicted the highest peak (238 g N₂O-N kg^–1 soil d^–1) at the beginning of the incubation, probably through a physical release. While the Tavy soil showed some NO₃ ^– accumulation at the end of the study with a maximum N₂O flux of 206 g N₂O-N kg^–1 soil d^–1, both belong to Oxisols. The other six soils, viz. Rengam, Selangor, Briah, Bungor, Serdang and Malacca series, formed smaller but maximum peaks in an decreasing order of 116 to 36 g N₂O-N kg^–1 soil d^–1. Liming the Oxisols and Ultisols raised the soil pH, resulting in NO₃ ^– accumulation and N₂O production to some extent. As such the highest N₂O flux of 130.2 and 77.4 g N₂O-N kg^–1 soil d^–1 was detected from the Bungor and Malacca soils, respectively. The Selangor soil, belonging to Inceptisol, did not respond to lime treatment. The respective total N₂O formations were 3.63, 1.92 and 1.69 mg N₂O-N kg^–1 soil from the Bungor, Malacca and Selangor soils, showing an increase by 49 and 99% over the former two non-limed soils. Under non-limed conditions, the indigenous soil properties, viz. Ca⁺⁺ content, %clay, %sand and pH of the soils collectively could have influenced the total N₂O formation.     

Soil water content and freezing temperature affect freeze–thaw related N2O production in organic soil

An organic agricultural soil was exposed to freeze–thaw cycles (FTC) using either intact soil cores or cores packed with homogenized soil. The cores were first exposed to two mild FTCs (–1.5°C/+4°C) with soil water content being 56–85% of the water-filled pore space (WFPS). Both intact and packed soil cores showed high N₂O emissions when the soil was thawing and had high WFPS. The second freeze–thaw cycle induced lower N₂O emission than the first. After the mild FTCs, a deep frost (–15°C) was applied. This greatly increased the N₂O emissions when the soil was thawing. Freezing–thawing had a smaller effect on CO₂ than on N₂O release. The results show that both soil moisture and the severity of frost modify the N₂O burst after thawing, and N₂O release (denitrification) was favoured more by FTC than heterotrophic microbial activity (CO₂ production) in general. The possible reason for this difference is discussed.     

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.     

Effects of deep application of urea on NO and N2O emissions from an Andisol

A modeling study revealed that the depth of nitric oxide (NO) production in soil is crucial for its flux, while that of nitrous oxide (N₂O) is not. To verify this result, laboratory experiments with soil columns classified as Andisol (Hydric Hapludand) were conducted, with changing the depth of urea application, at 0–0.1 or 0.1–0.2 m. All the NO concentration profiles in soil exhibited a sharp peak at each fertilized layer within 5 days of fertilizer application. NO concentration in soil decreased abruptly as the distance from the fertilized layer increased. These findings imply that NO is produced mainly within the fertilized layer, but does not diffuse widely in the soil columns, because of rapid NO uptake within the soil. As a result, the NO flux from soil columns fertilized at 0.1–0.2 m depth over the 48-day study period was reduced to almost the same rate as that of the unfertilized one. The total NO emissions from soil columns unfertilized and fertilized at 0–0.1 and 0.1–0.2 m depth were 0.02, 1.39 (± 0.05) and 0.05 (± 0.03) kg N ha^–1, respectively, suggesting that NO emission derived from N fertilizer could be reduced to 2% by shifting the depth of fertilizer application by 0.1 m. On the other hand, soil N₂O concentration profiles exhibited a gentler peak, because of the lower uptake by soil. N₂O fluxes were affected more by the soil conditions, e.g. soil water content, than the distance between fertilized depth and soil surface. The total N₂O emissions from soil columns unfertilized and fertilized at 0–0.1 and 0.1–0.2 m were 0.02, 0.16 (± 0.03) and 0.25 (± 0.04) kg N ha^–1, respectively.     

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.     

Greenhouse gas emissions from tropical peatlands of Kalimantan,Indonesia

Greenhouse gas emissions were measured from tropical peatlands of Kalimantan, Indonesia. The effect of hydrological zone and land-use on the emission of N₂O, CH₄ and CO₂ were examined. Temporal and annual N₂O, CH₄ and CO₂ were then measured. The results showed that the emissions of these gases were strongly affected by land-use and hydrological zone. The emissions exhibited seasonal changes. Annual emission of N₂O was the highest (nearly 1.4 g N m^–2y^–1) from site A-1 (secondary forest), while there was no signi.cant difference in annual N₂O emission from site A-2 (paddy field) and site A-3 (rice-soybean rotation field). Multiplying the areas of forest and non-forest in Kalimantan with the emission of N₂O from corresponding land-uses, the annual N₂O emissions from peat forest and peat non-forest of Kalimantan were estimated as 0.046 and 0.004 Tg N y^–1, respectively. The emissions of CH₄ from paddy field and non-paddy field were estimated similarly as 0.14 and 0.21 Tg C y^–1, respectively. Total annual CO₂ emission was estimated to be 182 Tg C y^–1. Peatlands of Kalimantan, Indonesia, contributed less than 0.3 of the total global N₂O, CO₂ or CH₄ emission, indicating that the gaseous losses of soil N and C from the study area to the atmosphere were small.     

Effects of the depth of NO and N2O productions in soil on their emission rates to the atmosphere: analysis by a simulation model

Many factors are concerned in the changing forms of nitrogen compounds in soil, so it is not easy to make precise models to simulate the concentration profiles of soil nitric oxide (NO) and nitrous oxide (N₂O) and their emission rates under various soil conditions. We prepared a simple mathematical simulation model based on soil concentration profiles of NO and N₂O. The profiles were measured at lysimeters filled with Andosol soil and fertilized with ammonium sulfate at rate of 200 kgNha^-1, incorporating to plow layer (Hirose & Tsuruta, 1996). In this model, diffusion of gases in soil followed Fick's law and the diffusion coefficient was adopted from Sallam et al. (1984). The gas production rate was set up at constant value in the site of gas production, and the gaseous consumption followed Michaelis-Menten kinetics. By changing only the depth of NO and N₂O production in soil in this model, we obtained the following results.(1) When the depth of gas production was set at near the soil surface (NO: 0–10 cm, N₂O: 0-8 cm), the emission rates of both gases corresponded with the results of the lysimeter-measurement.(2) When the depth of gas production was shifted down 10 cm deeper (NO: 10–20 cm, N₂O: 10-18 cm), the gas emission rate of NO decreased to 1.3% of (1), while that of N₂O was almost the same as (1).(3) In the case that the total intensity of produced gases was not changed from (1) or (2), but that the extent of gas productions expanded 3 times wider (NO: 0–30 cm, N₂O: 0–24 cm) than (1) or (2), the emission rates of NO and N₂O became 26% and 95% of (1), respectively.The above results suggest the possibility of mitigating NO emission by setting the site of gaseous production in deeper soil, e.g. by means of deep application of fertilizer.     

Impact of different forms of N fertilizer on N2O emissions from intensive grassland

Nitrous oxide (N₂O) emissions were measured over two years from an intensively managed grassland site in the UK. Emissions from ammonium nitrate (AN) and urea (UR) were compared to those from urea modified by various inhibitors (a nitrification inhibitor, UR(N), a urease inhibitor, UR(U), and both inhibitors together, SU), as well as a controlled release urea (CR). N₂O fluxes varied through time and between treatments. The differences between the treatments were not consistent throughout the year. After the spring and early summer fertilizer applications, fluxes from AN plots were greater than fluxes from UR plots, e.g. the cumulative fluxes for one month after N application in June 1999 were 5.2 ± 1.1 kg N₂O-N ha^–1 from the AN plots, compared to 1.4 ± 1.0 kg N₂O-N ha^–1 from the UR plots. However, after the late summer application, there was no difference between the two treatments, e.g. cumulative fluxes for the month following N application in August 2000 were 3.3 ± 0.7 kg N₂O-N ha^–1 from the AN plots and 2.9 ± 1.1 kg N₂O-N ha^–1 from the UR plots. After all N applications, fluxes from the UR(N) plots were much less than those from either the AN or the UR plots, e.g. 0.2 ± 0.1 kg N₂O-N ha^–1 in June 1999 and 1.1 ± 0.3 kg N₂O-N ha^–1 in August 2000. Combining the results of this experiment with earlier work showed that there was a greater N₂O emission response to rainfall around the time of fertilizer application in the AN plots than in the UR plots. It was concluded that there is scope for reducing N₂O emissions from N-fertilized grassland by applying UR instead of AN to wet soils in cool conditions, e.g. when grass growth begins in spring. Applying UR with a nitrification inhibitor could cut emissions further.     

Emissions of N2O from Scottish agricultural soils, as a function of fertilizer N

Potato fields and cut (ungrazed) grassland in SE Scotland gave greater annual N₂O emissions per ha (1.0–3.2 kg N₂O–N ha^-1) than spring barley or winter wheat fields (0.3–0.8 kg N₂O–N ha^-1), but in terms of emission per unit of N applied the order was potatoes > barley > grass > wheat. On the arable land, especially the potato fields, a large part of the emissions occurred after harvest.When the grassland data were combined with those for 2 years' earlier work at the same site, the mean emission over 3 years, for fertilization with ammonium nitrate, was 2.24 kg N₂O–N ha^-1 (0.62% of the N applied). Also, a very strong relationship between N₂O emission and soil nitrate content was found for the grassland, provided the water-filled pore space was > 70%. Significant relationships were also found between the emissions from potato fields and the soil mineral N content, with the added feature that the emission per unit of soil mineral N was an order of magnitude larger after harvest than before, possibly due to the effect of labile organic residues on denitrification.Generally the emissions measured were lower, as a function of the N applied, than those used as the basis for the current value adopted by IPCC, possibly because spring/early summer temperatures in SE Scotland are lower than those where the other data were obtained. The role of other factors contributing to emissions, e.g. winter freeze–thaw events and green manure inputs, are discussed, together with the possible implications of future increases in nitrogen fertilizer use in the tropics.     

Nitrogen losses from fertilizers applied to maize, wheat and rice in the North China Plain

Ammonia volatilization, denitrification loss and total nitrogen (N) loss (unaccounted-for N) have been investigated from N fertilizer applied to a calcareous sandy loam fluvo-aquic soil at Fengqiu in the North China Plain. Ammonia volatilization was measured by the micrometeorological mass balance method, denitrification by the acetylene inhibition – soil core incubation technique, and total N loss by ¹⁵N-balance technique. Ammonia loss was an important pathway of N loss from N fertilizer applied to rice (30–39% of the applied N) and maize (11–48%), but less so for wheat (1–20%). The amounts of unaccounted-for fertilizer N were in the order of rice > maize > wheat. Deep placement greatly reduced ammonia volatilization and total N loss. Temperature, wind speed, and solar radiation (particular for rice), and source of N fertilizer also affect extent and pattern of ammonia loss. Denitrification (its major gas products are N₂ and N₂O) usually was not a significant pathway of N loss from N fertilizer applied to maize and wheat. The amount of N₂O emission (N₂O is an intermediate product from both nitrification and denitrification) was comparable to denitrification loss for maize and wheat, and it was not significant in the economy of fertilizer N in agronomical terms, but it is of great concern for the environment.