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.     

Emission of nitrous oxide from soils used for agriculture

Nitrous oxide is emitted into the atmosphere as a result of biomass burning, and biological processes in soils. Biomass burning is not only an instantaneous source of nitrous oxide, but it results in a longer term enhancement of the biogenic production of this gas. Measurements of nitrous oxide emissions from soils before and after a controlled burn showed that significantly more nitrous oxide was exhaled after the burn. The current belief is that 90% of the emissions come from soils. Nitrous oxide is formed in soils during the microbiological processes nitrification and denitrification. Because nitrous oxide is a gas it can escape from soil during these transformations. Nitrous oxide production is controlled by temperature, pH, water holding capacity of the soil, irrigation practices, fertilizer rate, tillage practice, soil type, oxygen concentration, availability of carbon, vegetation, land use practices and use of chemicals. Nitrous oxide emissions from agricultural soils are increased by the addition of fertilizer nitrogen and by the growth of legumes to fix atmospheric nitrogen. A recent analysis suggests that emissions of nitrous oxide from fertilized soils are not related to the type of fertilizer nitrogen applied and emissions can be calculated from the amount of nitrogen applied. Legumes also contribute to nitrous oxide emission in a number of ways, viz. atmospheric nitrogen fixed by legumes can be nitrified and denitrified in the same way as fertilizer nitrogen, thus providing a source of nitrous oxide, and symbiotically living Rhizobia in root nodules are able to denitrify and produce nitrous oxide. Conversion of tropical forests to crop production and pasture has a significant effect on the emission of nitrous oxide. Emissions of nitrous oxide increased by about a factor of two when a forest in central Brazil was clear cut, and pasture soils in the same area produced three times as much nitrous oxide as adjacent forest soils. Studies on temperate and tropical rice fields show that less than 0.1% of the applied nitrogen is emitted as nitrous oxide if the soils are flooded for a number of days before fertilizer application. However, if mineral nitrogen is present in the soil before flooding it will serve as a source of nitrous oxide during wetting and drying cycles before permanent flooding. Thus dry seeded rice can be a source of considerable nitrous oxide. There are also indirect contributions to nitrous oxide emission through volatilization of ammonia and emission of nitric oxides into the atmosphere, and their redistribution over the landscape through wet and dry deposition. In general nitrous oxide emissions can be decreased by management practices which optimize the crop's natural ability to compete with processes whereby plant available nitrogen is lost from the soil-plant system. If these options were implemented they would also result in increased productivity and reduced inputs. This revised version was published online in August 2006 with corrections to the Cover Date.     

A study of nitrous oxide decomposition over calcium oxide

A study of N₂O decomposition reaction in a fixed bed a reactor over bed of CaO particles has been conducted. Effects of parameters such as concentration of inlet N₂O gas, reacting temperature and content of CO₂/ CO gas present in the reacting materials on the decomposition reaction have been investigated. The results showed that the conversion of N₂O decomposition was accelerated by the increase of reaction temperature, and the existence of CO, while the rate was hindered by the existence of CO₂. Heterogeneous gas solid reaction kinetics was proposed for N₂O decomposition and compared with homogeneous reaction kinetics. Presented at the Int’l Symp. on Chem. Eng. (Cheju, Feb. 8–10, 2001), dedicated to Prof. H. S. Chun on the occasion of his retirement from Korea University.     

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.     

Direct decomposition of nitrous oxide in the presence of oxygen over iridium catalyst supported on alumina

Direct decomposition of nitrous oxide (N₂O) on noble metal catalysts supported on alumina was examined in the presence of oxygen. The iridium catalysts supported on alumina showed higher activities than the other noble metal catalysts. Although the catalyst activity was affected by oxygen formed by N₂O decomposition at lower temperatures, desorption of oxygen proceeded promptly at the temperature , and the catalytic activity was recovered by increasing the reaction temperature from 350 to . Therefore, the Ir/Al₂O₃ catalyst can be used for N₂O decomposition in the presence of oxygen at relatively higher temperatures.     

Effects of fertiliser type and the presence or absence of plants on nitrous oxide emissions from irrigated soils

Nitrous oxide (N₂O) emissions and denitrification losses from an irrigated sandy loam soil amended with composted municipal solid waste (MSW), sheep manure (SM), surface applied pig slurry (SPS), incorporated pig slurry (IPS) or urea (U) were studied under Mediterranean conditions. We quantified emissions, in both the presence and absence of maize and N₂O production, via denitrification and nitrification pathways using varying concentrations of acetylene. Discounting the N₂O lost in the Control, the percentages of N₂O lost in relation to the total N applied were greater for urea (1.80%) than for MSW (0.50%), SM (0.46%), SPS (1.02%) or IPS (1.27%). In general, plots treated with organic fertilisers emitted higher amounts of N₂O when under maize than bare soil plots. On the other hand, greater denitrification losses were also recorded for plots in the absence of plants (between 9.7 and 29.3 kg N₂O-N ha⁻¹) than for areas with plants (between 7.1 and 24.1 kg N₂O-N ha⁻¹). The proportion of N₂O produced via denitrification was greater from fertiliser treatments than for the controls and also greater without plants (between 66 and 91 % of the N₂O emitted) than with plants (between 48 and 81%).     

Ammonia and nitrous oxide emissions from grass and alfalfa mulches

Ammonia (NH₃) and nitrous oxide (N_-2O) emissions were measured in the field for three months from three different herbage mulches and from bare soil, used as a control. The mulches were grass with a low N-content (1.15% N in DM), grass with a high N-content (2.12% N in DM) and alfalfa with a high N-content (4.33% N in DM). NH₃ volatilization was measured using a micrometeorological technique. N_-2O emissions were measured using closed chambers. NH₃ and N_-2O emissions were found to be much higher from the N-rich mulches than from the low-N grass and bare soil, which did not differ significantly. Volatilization losses of NH₃ and N_-2O occurred mainly during the first month after applying the herbage and were highest from wet material shortly after a rain. The extent of NH₃-N losses was difficult to estimate, due to the low frequency of measurements and some problems with the denuder technique, used on the first occasions of measurements. Nevertheless, the results indicate that NH₃-N losses from herbage mulch rich in N can be substantial. Estimated losses of NH₃-N ranged from the equivalent of 17% of the applied N for alfalfa to 39% for high-N grass. These losses not only represent a reduction in the fertilizer value of the mulch, but also contribute appreciably to atmospheric pollution. The estimated loss of N_-2O-N during the measurement period amounted to 1% of the applied N in the N-rich materials, which is equivalent to at least 13 kg N_-2O-N ha^-1 lost from alfalfa and 6 kg ha^-1 lost from high-N grass. These emission values greatly exceed the 0.2 kg N_-2O-N ha^-1 released from bare soil, and thus contribute to greenhouse gas emissions.     

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.     

Electroreduction of nitrous oxide on platinum and palladium: Toward selective catalysts for methanol–nitrous oxide mixed-reactant fuel cells

The kinetics of N₂O electroreduction in the absence and presence of methanol was studied between 295 and 333 K on polycrystalline Pt and Pd electrodes in 0.1 M NaOH. In the absence of methanol the reduction of N₂O on Pd is more facile than on Pt as shown by the approximately four times lower apparent activation energy and lower Tafel slope (Pt: 0.111 ± 0.019 V dec⁻¹, Pd: 0.084 ± 0.007 V dec⁻¹ at 295 K). Two different electroreduction mechanisms are proposed for Pt and Pd with and without participation of underpotential deposited hydrogen, respectively. The selectivity of Pt and Pd electrodes toward both N₂O electroreduction and methanol (0.5 and 1 M) oxidation at 295 K was also investigated. Pt based electrocatalysts are promising candidates for the anode of a mixed reactant CH₃OH–N₂O fuel cell due to inhibition of N₂O reduction by chemisorbed methanol. Pd on the other hand is a selective cathode electrocatalyst since N₂O reduction takes place fairly actively in the presence of 1 M methanol, while methanol oxidation is inhibited.     

Fluxes of methane and nitrous oxide in water-saving rice production in north China

Lowland rice production is currently facing serious water shortages in numerous Asian countries. In the North China Plain water limitations are severe. Water-saving rice production techniques are therefore increasingly searched for. Here we present the first study of trace gas emissions from a water-saving rice production system where soils are mulched and are kept close to field capacity in order to compare their contribution to global warming with traditional paddy rice. In a two-year field experiment close to Beijing, CH₄ and N₂O fluxes were monitored in two forms of the Ground Cover Rice Production System (GCRPS) and in traditional paddy fields using closed chambers. With paddy rice the observed CH₄ emissions were very low, about 0.3 g CH₄ m⁻² a⁻¹ in 2001 and about 1 g CH₄ m⁻² a⁻¹ in 2002. In GCRPS, the CH₄ emissions were negligible. N₂O fluxes in GCRPS were similar, 0.5 to 0.6 g N₂O m⁻² a⁻¹ in 2001 and 2002, and emission peaks mainly followed fertilizer applications. In paddy rice, N₂O fluxes were unexpectedly low throughout the year 2001 (0.03 g N₂O m⁻² a⁻¹), and in 2002 larger emissions occurred during the drainage period. So with 0.4 g N₂O m⁻² a⁻¹ the cumulative flux was similar to emissions in GCRPS. Total CO₂ equivalent fluxes calculated according to IPCC methodology were tenfold higher in GCRPS compared to paddy in 2001. In 2002, fluxes from both systems were similar with 175 and 141 g CO₂ equivalents m⁻² a⁻¹ from GCRPS and paddy. Burkhard Sattelmacher deceased.     

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.     

Isotopic study of nitrous oxide decomposition on an oxidized Rh catalyst: mechanism of oxygen desorption

N₂O decomposition on an oxidized Rh catalyst (unsupported) has been studied using a tracer technique in order to reveal the reaction mechanism. N₂ ¹⁶O was pulsed onto an ¹⁸O/oxidized Rh catalyst at 493 K and desorbed O₂ molecules were monitored. The ¹⁸O fraction in the desorbed oxygen had the same value as that on the surface oxygen. The result shows that the oxygen molecules do not desorb via the Eley–Rideal mechanism, but via the Langmuir–Hinshelwood mechanism. On the other hand, desorption of oxygen from Rh surfaces (in vacuum or in He) occurs at higher temperatures, which suggests reaction-assisted desorption of oxygen during the N₂O decomposition reaction at low temperature. This revised version was published online in July 2006 with corrections to the Cover Date.     

The photocatalytic reduction of nitrous oxide with propane on lead(II) ion-exchanged ZSM-5 catalysts

UV irradiation of the Pb²⁺/ZSM-5 catalyst prepared by an ion-exchange method in the presence of N₂O leads to the decomposition of N₂O into N₂. This reaction is found to be dramatically enhanced by the addition of propane to produce N₂ and oxygen-containing compounds such as ethanol or acetone. UV light effective for the reaction lies in wavelength regions shorter than 250 nm where the absorption band of the Pb²⁺ ion ([Xe] 4f¹⁴5d¹⁰6s² [Xe] 4f¹⁴5d¹⁰6s¹6p¹) exists, indicating that the excited state of the isolated Pb²⁺ ions plays a significant role in this decomposition of N₂O both in the absence and the presence of propane, and the role of propane is found to be a capture of oxygen atoms formed by the decomposition of N₂O.     

Effect of noble metals in the decomposition of nitrous oxide over Fe-ferrierites

The decomposition of nitrous oxide was studied over Fe-ferrierite, Me-ferrierites and Fe/Me-ferrierites (Me: Pt, Rh and Ru). Flow as well as batch experiments were carried out and showed a synergy between Fe and Me ions. Ions of noble metals in Fe-ferrierite increased the catalytic activity in the sequence Pt < Rh ≅ Ru. Addition of NO substantially decreased the decomposition of N₂O over Rh/ferrierite and Ru/ferrierite, but not over bimetallic ferrierites. NO _x species created during the decomposition of nitrous oxide alone as well as with addition of NO, and employment of nitrous oxide labeled with ¹⁸O allowed us to assume a changing decomposition mechanism in the presence of Me ions in Fe-ferrierites.     

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.     

生活污水不同生物脱氮过程中N_2O产量及控制

利用好氧-缺氧SBR反应器和全程曝气SBBR反应器处理生活污水,分别实现了全程、短程和同步硝化反硝化脱氮过程,研究了不同脱氮过程中N2O的产生及释放情况,同时考察了不同DO条件下同步脱氮效率及N2O产生量。结果表明,全程、短程生物脱氮过程中N2O主要产生于硝化过程,反硝化过程有利于降低系统N2O产量。全程、短程、同步硝化反硝化脱氮过程中N2O产量分别为4.67、6.48和0.35mg.L-1。硝化过程中NO2-N的积累是导致系统N2O产生的主要原因。部分AOB在限氧条件下以NH4+-N作为电子供体,NO2-N作为电子受体进行反硝化,最终产物是N2O。不同DO条件下同步硝化反硝化过程中N2O的产生表明:控制SBBR系统中DO浓度达到稳定的同步脱氮效率可使系统N2O产量最低。     

Nitrogen inputs to rivers, estuaries and continental shelves and related nitrous oxide emissions in 1990 and 2050: a global model

The purpose of the current paper is to estimate future trends (up to the year 2050) in the global geographical distribution of nitrous oxide (N₂O) emissions in rivers, estuaries, and continental shelf regions due to biological processes, particularly as they are affected by anthropogenic nitrogen (N) inputs, and to compare these to 1990 emissions. The methodology used is from Seitzinger and Kroeze (1998) who estimated 1990 emissions assuming that N₂O production in these systems is related to nitrification and denitrification. Nitrification and denitrification in rivers and estuaries were related to external inputs of nitrogen to those systems. The model results indicate that between 1990 and 2050 the dissolved inorganic nitrogen (DIN) export by rivers more than doubles to 47.2 Tg N in 2050. This increase results from a growing world population, associated with increases in fertilizer use and atmospheric deposition of nitrogen oxides (NOy). By 2050, 90% of river DIN export can be considered anthropogenic. N₂O emissions from rivers, estuaries and continental shelves are calculated to amount to 4.9 (1.3 – 13.0) Tg N in 2050, of which two-thirds are from rivers. Aquatic emissions of N₂O are calculated to increase faster than DIN export rates: between 1990 and 2050, estuarine and river emissions increase by a factor of 3 and 4, respectively. Emissions from continental shelves, on the other hand, are calculated to increase by only 12.5%.     

Preliminary studies on N2O emission fluxes from upland soils and paddy soils in China

In this paper, we presented the preliminary results of N₂O fluxes from Chinese upland and rice paddy fields. The mean N₂O flux from upland fields of North China is 30.6 μg N₂O-N m^-2 h^-1; the average N₂O flux from Chinese rice paddy field is 39.5 μg N₂O-N m^-2 h^-1. The effects of cropping system, water management and application of N fertilizer and organic manure on N₂O emission from rice paddy field have also been presented. This revised version was published online in August 2006 with corrections to the Cover Date.     

Fluxes of nitrous oxide from soil under different crop rotations and tillage systems in the South of Brazil

The zero tillage (ZT) system is used in a large area (>24 Mha) of crop production in Brazil. This management system can contribute to soil C sequestration, but many studies in other countries have registered greater nitrous oxide emissions under ZT compared to conventional tillage (CT), which may reduce greenhouse gas mitigation benefits. The aim of this study was to estimate the emission of N₂O from cropping systems under conventional and zero tillage in an 18-year-old experiment conducted on a Rhodic Ferralsol in the South of Brazil. Fluxes of N₂O were measured over two years using static-closed chambers in the two tillage systems with three crop rotations. Soil water filled pore space (%WFPS) and soil mineral N were monitored along with rainfall and air temperature. Estimates of N₂O emissions were obtained by integrating the fluxes with time and also by applying the IPCC direct emission factor (EF1 = 1%) to the amounts of N added as fertilisers and returned as crop residues. Fluxes of N₂O were relatively low, apart from a short period at the beginning of measurements. No relationship between N₂O fluxes and %WFPS or mineral N were observed. Nitrous oxide emissions were not influenced either by tillage system or crop rotation. For the crop rotation receiving high rates of N fertiliser in the second year, field-measured N₂O emissions were significantly underestimated by the IPCC emission factor 1 (EF1). For the other treatments measured N₂O emissions fell within the EF1 uncertainty range, but always considerably lower than the EF1 estimate, which suggests IPCC EF1 overestimates true N₂O emissions for the Ferralsol under evaluation.     

NO and N2O emissions from savanna soils following the first simulated rains of the season

Data on the emissions of oxides of nitrogen from the soil during the early part of the wet season are reported for nutrient-rich and nutrient-poor sandy soils at Nylsvley, South Africa. The emissions of NO_x and N₂O following the first wetting event of the season are elevated relative to subsequent events. The observed high emission rates (76 ng N-NO m^-2 s^-1) are partially attributed to the sandiness of the soil, which permits NO to diffuse out of the soil rapidly. The pulse of high emissions following wetting is maintained for approximately 72 hours, thereafter continuing at around 20 ng NO m^-2 s^-1 while the soil remains moist. The initial pulse is suggested to be due to the accumulation of a substrate pool during the dry period, coupled with an inability of plants and microbes to use it effectively during the first few days after wetting. There were no significant differences in the peak or subsequent emission rates for either NO or N₂O between two sites of differing nitrogen mineralisation potentials. N₂O emissions averaged 8% of NO_x emissions. The enhanced emissions of NO_x which follow the first wetting after a prolonged dry period do not make a very large contribution to the annual gaseous N emission budget, but could be a significant contributor to the high tropospheric ozone levels observed over southern Africa in springtime.