Influence of soil properties on the turnover of nitric oxide and nitrous oxide by nitrification and denitrification at constant temperature and moisture

 Soils are a major source of atmospheric NO and N₂O. Since the soil properties that regulate the production and consumption of NO and N₂O are still largely unknown, we studied N trace gas turnover by nitrification and denitrification in 20 soils as a function of various soil variables. Since fertilizer treatment, temperature and moisture are already known to affect N trace gas turnover, we avoided the masking effect of these soil variables by conducting the experiments in non-fertilized soils at constant temperature and moisture. In all soils nitrification was the dominant process of NO production, and in 50% of the soils nitrification was also the dominant process of N₂O production. Factor analysis extracted three factors which together explained 71% of the variance and identified three different soil groups. Group I contained acidic soils, which showed only low rates of microbial respiration and low contents of total and inorganic nitrogen. Group II mainly contained acidic forest soils, which showed relatively high respiration rates and high contents of total N and NH₄ ⁺. Group III mainly contained neutral agricultural soils with high potential rates of nitrification. The soils of group I produced the lowest amounts of NO and N₂O. The results of linear multiple regression conducted separately for each soil group explained between 44–100% of the variance. The soil variables that regulated consumption of NO, total production of NO and N₂O, and production of NO and N₂O by either nitrification or denitrification differed among the different soil groups. The soil pH, the contents of NH₄ ⁺, NO₂ ^– and NO₃ ^–, the texture, and the rates of microbial respiration and nitrification were among the important variables. Received: 28 October 1999     

Estimation of simultaneous nitrification and denitrification in grassland soil associated with urea-N using 15N and nitrification inhibitor

 A low efficiency of use of N fertilisers has been observed in mid-Wales on permanent pasture grazed intensively by cattle. Earlier laboratories studies have suggested that heterogeneity in redox conditions at shallow soil depths may allow nitrification and denitrification to occur concurrently resulting in gaseous losses of N from both NH₄ ⁺ and NO₃ ^–. The objective of the investigation was to test the hypothesis that both nitrification and denitrification can occur simultaneously under simulated field capacity conditions (∼5 kPa matric potential). Intact soil cores were taken from grassland subjected to both grazing and amenity use. The fate of applied NH₄ ⁺ was examined during incubation. ¹⁵N was used as a tracer. Nitrapyrin was used as a nitrification inhibitor and acetylene was used to block N₂O reductase. More than 50% of N applied as NH₄ ⁺ disappeared over a period of 42 days from the soil mineral-N pool. Some of this N was evolved as N₂O. Accumulation of NO₃ ^––N in the surface 0–2.5 cm indicated active nitrification. Addition of nitrapyrin increased N recovery by 26% and inhibited both the accumulation of NO₃–N and emission of N₂O. When intact field cores were incubated after addition of ¹⁵N-urea, all of the N₂O evolved was derived from added urea-N. It was concluded that nitrification and denitrification do occur simultaneously in the top 7.5 cm or so, of the silty clay loam grassland topsoils of mid-Wales at moisture contents typical of field capacity. The quantitative importance of these concurrent processes to N loss from grassland systems has not yet been assessed. Received: 15 December 1998     

Nitrous oxide emissions from grassland and spring barley, following N fertiliser application with and without nitrification inhibitors

The aims of this study were to assess the effectiveness of the nitrification inhibitors dicyandiamide (DCD) and nitrapyrin on reducing emissions of nitrous oxide (N₂O) following application of NH₄ ⁺ or NH₄ ⁺-forming fertilisers to grassland and spring barley. DCD was applied to grassland with N fertiliser applications in April and August in 1992 and 1993, inhibiting N₂O emissions by varying amounts depending on the fertiliser form and the time of application. Over periods of up to 2 months following each application of DCD, emissions of N₂O were reduced by 58–78% when applied with urea (U) and 41–65% when applied with ammonium sulphate (AS). Annual emissions (April to March) of N₂O were reduced by up to 58% and 56% in 1992–1993 and 1993–1994, respectively. Applying DCD to ammonium nitrate (AN) fertilised grassland did not reduce emissions after the April 1993 fertilisation, but emissions following the August application were reduced. Nitrapyrin was only applied once, with the April fertiliser applications in 1992, reducing N₂O emissions over the following 12 months by up to 40% when applied with U. When N fertiliser was applied in June without DCD, the DCD applied in April was still partly effective; N₂O emissions were reduced 50%, 60% and 80% as effectively as the emissions following the April applications, for AS in 1993, U in 1992 and 1993, respectively. In 1992 the persistence of an inhibitory effect was greater for nitrapyrin than for DCD, increasing after the June fertiliser application as overall emissions from U increased. There was no apparent reduction in effectiveness following repeated applications of DCD over the 2 years. N₂O emissions from spring barley, measured only in 1993, were lower than from grassland. DCD reduced emissions from applied U by 40% but there was no reduction with AN. The results demonstrate considerable scope for reducing emissions by applying nitrification inhibitors with NH₄ ⁺ or NH₄ ⁺-forming fertilisers; this is especially so for crops such as intensively managed grass where there are several applications of fertiliser nitrogen per season, as the effect of inhibitors applied in April persists until after a second fertiliser application in June. Received: 30 August 1996     

A method of selective inhibition to distinguish between nitrification and denitrification as sources of nitrous oxide in soil

Summary Nitrapyrin and C₂H₂ were evaluated as nitrification inhibitors in soil to determine the relative contributions of denitrification and nitrification to total N₂O production. In laboratory experiments nitrapyrin, or its solvent xylene, stimulated denitrification directly or indirectly and was therefore considered unsuitable. Low partial pressures of C₂H₂ (2.5–5.0 Pa) inhibited nitrification and had only a small effect on denitrification, which made it possible to estimate the contribution of denitrification. The contribution of nitrification was estimated by subtracting the denitrification value from total N₂O production (samples without C₂H₂). The critical C₂H₂ concentrations needed to achieve inhibition of nitrification, without affecting the N₂O reductase in denitrifiers, must be individually determined for each set of experimental conditions.     

Recovery of nitrification and production of NO and N2O after exposure of soil to acetylene

Incubation of soil under low partial pressures of acetylene (10 Pa) is a widely used method to specifically inhibit nitrification due to the suicide inhibition of ammonium monooxygenase (AMO), the first enzyme in NH₄ ⁺ oxidation by nitrifying bacteria. Although the inhibition of AMO is irreversible, recovery of activity is possible if new enzyme is synthesized. In experiments with three different soils, NH₄ ⁺ concentrations decreased and NO₃ ^– concentrations increased soon after acetylene was removed from the atmosphere. Recovery of NO production started immediately after the removal of acetylene. The release rates of NO and N₂O were higher in soil samples which were only preincubated with 10 Pa acetylene than in those which were kept in the presence of 10 Pa acetylene. In the permanent presence of 10 Pa acetylene, NH₄ ⁺ and NO₃ ^– concentrations stayed constant, and the release rates of NO and N₂O were low. These low release rates were apparently due to processes other than nitrification. Our experiments showed that the blockage of nitrification by low (10 Pa) acetylene partial pressures is only reliable when the soil is kept in permanent contact with acetylene. Received: 17 July 1996     

Effect of wax-coated calcium carbide and nitrapyrin on nitrogen loss and methane emission from dry-seeded flooded rice

Summary The effectiveness of wax-coated calcium carbide (as a slow-release source of acetylene) and nitrapyrin in inhibiting nitrification and emission of the greenhouse gases N₂O and CH₄ was evaluated in a microplot study with dry-seeded flooded rice grown on a grey clay near Griffith, NSW, Australia. The treatments consisted of factorial combinations of N levels with nitrification inhibitors (control, wax-coated calcium carbide, and nitrapyrin). The rate of nitrification was slowed considerably by the addition of wax-coated calcium carbide, but it was inhibited only slightly by the addition of nitrapyrin. As a result, the emission of N₂O was markedly reduced by the application of wax-coated calcium carbide, whereas there was no significant difference in rates of N₂O emission between the control and nitrapyrin treatments. Both nitrification inhibitors significantly reduced CH₄ emission, but the lowest emission rates were observed in the wax-coated calcium carbide treatment. At the end of the experiment 84% of the applied N was recovered from the wax-coated calcium carbide treatment compared with 43% for the nitrapyrin and control treatments.     

Laboratory investigations into the effects of the pesticides mancozeb, chlorothalonil, and prosulfuron on nitrous oxide and nitric oxide production in fertilized soil

Independent soil microcosm experiments were used to investigate the effects of the fungicides mancozeb and chlorothalonil, and the herbicide prosulfuron, on N₂O and NO production by nitrifying and denitrifying bacteria in fertilized soil. Soil cores were amended with NH₄NO₃ or NH₄NO₃ and pesticide, and the N₂O and NO concentrations were monitored periodically for approximately 48 h following amendment. Nitrification is the major source of N₂O and NO in these soils at soil moistures relevant to those observed at the field site where the cores were collected. At pesticide concentrations from 0.02 to 10 times that of a standard single application on a corn crop, N₂O and NO production was inhibited by all three pesticides. Generally N₂O production was inhibited by the pesticides from 10 to 62% and 20 to 98% at the lowest and highest dosages, respectively. Nitric oxide production was generally inhibited from about 5 to 47% and by 20 to 97% at the lowest and highest dosages, respectively. Nitrous oxide and nitric oxide production by nitrification was more susceptible to inhibition by these pesticides than denitrification. Production of both N₂O and NO by nitrification was inhibited by as much as 99%, at the highest concentration of pesticide applied. The net production of N₂O increased as soil moisture increased. The rate of NO production was greatest at the intermediate moistures investigated, between 14 and 19% gravimetric soil moisture, suggestive that nitrification is the dominant source of NO.     

Nitrogen monoxide production and consumption in an organic soil

 Factors controlling NO production, consumption, and emission rates were examined in an organic soil. Emission rates were measured in the enclosed headspaces of intact soil cores under three fertilisation treatments (unfertilised or 100 kg N ha^–1 as NH₄Cl or as NaNO₃), with and without the nitrification inhibitor C₂H₂ (20–70 μl l^–1). Nitrification was always the main source of NO emitted across the soil surface, even when the soil was nearly saturated. Fertilisation of soil with NH₄Cl increased NO emission both by stimulating NO production from nitrification, and by decreasing the NO consumption rate constant. Addition of NaNO₃ also stimulated the production of NO and N₂O during nitrification in aerobic soil slurry experiments. This effect was eliminated by adding C₂H₂ and was therefore not related to denitrification. In loose soil samples, the increase in NO-N production after NH₄Cl addition represented as much as 26% of the added N. However, in intact cores, 95% of the NO produced through nitrification was oxidised within the soil column rather than emitted to the atmosphere. We concluded that nitrification is the primary NO source from this organic soil, that surface NO emissions are much lower than gross NO production rates, and that gaseous N oxide (NO and N₂O) losses during nitrification can be affected by both soil NH₄ ⁺ and NO₃ ^–. Received: 15 December 1998     

Immediate and adaptational temperature effects on nitric oxide production and nitrous oxide release from nitrification and denitrification in two soils

 Nitrification and denitrification are, like all biological processes, influenced by temperature. We investigated temperature effects on N trace gas turnover by nitrification and denitrification in two soils under two experimental conditions. In the first approach ("temperature shift experiment") soil samples were preincubated at 25  °C and then exposed to gradually increasing temperatures (starting at 4  °C and finishing at 40–45  °C). Under these conditions the immediate effect of temperature change was assessed. In the second approach ("discrete temperature experiment") the soil samples were preincubated at different temperatures (4–35  °C) for 5 days and then tested at the same temperatures. The different experimental conditions affected the results of the study. In the temperature shift experiment the NO release increased steadily with increasing temperature in both soils. In the discrete temperature experiment, however, the production rates of NO and N₂O showed a minimum at intermediate temperatures (13–25  °C). In one of the soils (soil B9), the percent contribution of nitrification to NO production in the discrete temperature experiment reached a maximum (>95% contribution) at 25  °C. In the temperature shift experiment nitrification was always the dominant process for NO release and showed no systematic temperature dependency. In the second soil (soil B14), the percent contribution of nitrification to NO release decreased from 50 to 10% as the temperature was increased from 4  °C to 45  °C, but no differences were evident in the discrete temperature experiment. The N₂O production rates were measured in the discrete temperature experiment only. The contribution of nitrification to N₂O production in soil B9 was considerably higher at 25–35  °C (60–80% contribution) than at 4–13  °C (15–20% contribution). In soil B14 the contribution of nitrification to N₂O production was lowest at 4  °C. The effects of temperature on N trace gas turnover differed between the two soils and incubation conditions. The experimental set-up allowed us to distinguish between immediate effects of short-term changes in temperature on the process rates, and longer-term effects by which preincubation at a particular temperature presumably resulted in the adaptation of the soil microorganisms to this temperature. Both types of effects were important in regulating the release of NO and N₂O from soil. Received: 20 October 1998     

Emissions of nitrous oxide from a constructed wetland using a groundfilter and macrophytes in waste-water purification of a dairy farm

 In less populated rural areas constructed wetlands with a groundfilter made out of the local soil mixed with peat and planted with common reed (Phragmites australis) are increasingly used to purify waste water. Particularly in the rhizosphere of the reed, nitrification and denitrification processes take place varying locally and temporally, and the question arises to what extent this type of waste-water treatment plant may contribute to the release of N₂O. In situ N₂O measurements were carried out in the two reed beds of the Friedelhausen dairy farm, Hesse, Germany, irrigated with the waste water from a cheese dairy and 70 local inhabitants (12 m³ waste water or 6 kg BOD₅ or 11 kg chemical O₂ demand (COD_Mn) day^–1). During November 1995 to March 1996, the release of N₂O was measured weekly at 1 m distances using eight open chambers and molecular-sieve traps to collect and absorb the emitted N₂O. Simultanously, the N₂O trapped in the soil, the soil temperature, as well as the concentrations of NH₄ ⁺-N, NO₃ ^–-N, NO₂ ^–-N, water-soluble C and the pH were determined at depths of 0–20, 20–40 and 40–60 cm. In the waste water from the in- and outflow the concentrations of COD_Mn, BOD₅, NH₄ ⁺-N, NO₃ ^–-N, NO₂ ^–-N, as well as the pH, were determined weekly. Highly varying amounts of N₂O were emitted at all measuring dates during the winter. Even at soil temperatures of –1.5  °C in 10 cm depth of soil or 2  °C at a depth of 50 cm, N₂O was released. The highest organic matter and N transformation rates were recorded in the upper 20 cm of soil and in the region closest to the outflow of the constructed wetland. Not until a freezing period of several weeks did the N₂O emissions drop drastically. During the period of decreasing temperatures less NO₃ ^–-N was formed in the soil, but the NH₄ ⁺-N concentrations increased. On average the constructed wetlands of Friedelhausen emitted about 15 mg N₂O-N inhabitant equivalent^–1 day^–1 during the winter period. Nitrification-denitrification processes rather than heterotrophic denitrification are assumed to be responsible for the N₂O production. Received: 28 October 1998     

Effect of biochar and nitrapyrin on nitrous oxide and nitric oxide emissions from a sandy loam soil cropped to maize

A field experiment was conducted to evaluate the combined or individual effects of biochar and nitrapyrin (a nitrification inhibitor) on N₂O and NO emissions from a sandy loam soil cropped to maize. The study included nine treatments: addition of urea alone or combined with nitrapyrin to soils that had been amended with biochar at 0, 3, 6, and 12 t ha^?1 in the preceding year, and a control without the addition of N fertilizer. Peaks in N₂O and NO flux occurred simultaneously following fertilizer application and intense rainfall events, and the peak of NO flux was much higher than that of N₂O following application of basal fertilizer. Mean emission ratios of NO/N₂O ranged from 1.11 to 1.72, suggesting that N₂O was primarily derived from nitrification. Cumulative N₂O and NO emissions were 1.00 kg N₂O-N ha^?1 and 1.39 kg NO-N ha^?1 in the N treatment, respectively, decreasing to 0.81–0.85 kg N₂O-N ha^?1 and 1.31–1.35 kg NO-N ha^?1 in the biochar amended soils, respectively, while there was no significant difference among the treatments. NO emissions were significantly lower in the nitrapyrin treatments than in the N fertilization-alone treatments (P?<?0.05), but there was no effect on N₂O emissions. Neither biochar nor nitrapyrin amendment affected maize yield or N uptake. Overall, our results showed that biochar amendment in the preceding year had little effect on N₂O and NO emissions in the following year, while the nitrapyrin decreased NO, but not N₂O emissions, probably due to suppression of denitrification caused by the low soil moisture content.     

Effect of the inhibitors nitrapyrin and sodium chlorate on nitrification and N2O formation in an acid forest soil

An acid forest soil from beech forest gaps, which were either limed or unlimed, and the undisturbed forest was investigated for the type of nitrifying populations and the process of N₂O evolution. To see whether nitrifiers were of heterotrophic or autotrophic origin, the nitrification inhibitors nitrapyrin and sodium chlorate were applied to disturbed soil samples which underwent laboratory incubations. Nitrapyrin inhibits autotrophic nitrification. In different studies, sodium chlorate has been identified as an inhibitor either of autotrophic or of heterotrophic nitrification. In the samples investigated only nitrapyrin inhibited the autotrophic nitrification occurring in the limed soil. Sodium chlorate effectively inhibited heterotrophic nitrification. In the limed forest floor samples, where most autotrophic nitrification occured, sodium chlorate showed no inhibitory effect. In another laboratory incubation experiment, N₂O evolution from undisturbed soil columns, to which the above inhibitors were applied, was investigated. In those samples, in which nitrification had been reduced, neither inhibitor significantly reduced N₂O evolution. Thus it was concluded that the contribution of nitrification to N₂O losses is negligible, and that N₂O evolution arises from the activity of denitrifying organisms. Microbial biomass and respiration measurements showed that the inhibitors did not affect microflora negatively.     

Field method to determine N2O emission from nitrification and denitrification

 Nitrous oxide (N₂O) emissions via the nitrification (I _nit) and denitrification (I _den) pathways were successfully measured with in-field incubation of soil cores in preserving jars at 0 Pa and 5–10 Pa acetylene. From the incubations, fractions of nitrification – N₂O over total N₂O (I _nit / I _tot) – and denitrification – N₂O over total N₂O (I _den / I _tot) – were obtained. Actual field emissions of N₂O via nitrification (F _nit) and denitrification (F _den) were calculated by multiplying the fractions from the incubation technique with the daily N₂O emission (F _day) determined with a direct soil cover method. The approach presented here was successful for a whole range of soil moisture conditions in intensive grassland. F _nit and F _den followed the trends of soil ammonium and soil nitrate. Received: 31 October 1997     

Responses of nitrous oxide, dinitrogen and carbon dioxide production and oxygen consumption to temperature in forest and agricultural light-textured soils determined by model experiment

 The experiment, carried out on a forest and arable light-textured soil, was designed to study the temperature response of autotrophic and heterotrophic N₂O production and investigate how the N₂O flux relates to soil respiration and O₂ consumption. Although N₂O production seemed to be stimulated by a temperature increase in both soils, the relationship between production rate and temperature was different in the two soils. This seemed to depend on the different contribution of nitrification and denitrification to the overall N₂O flux. In the forest soil, almost all N₂O was derived from nitrification, and its production rate rose linearly from 2  °C to 40  °C. A stronger effect of temperature on N₂O production was observed in the arable soil, apparently as a result of an incremental contribution of denitrification to the overall N₂O flux with rising temperature. The soil respiration rate increased exponentially with temperature and was significantly correlated with N₂O production. O₂ consumption stimulated denitrification in both soils. In the arable soil, N₂O and N₂ production increased exponentially with decreasing O₂ concentration, though N₂O was the main gas produced at any temperature. In the forest soil, only the N₂ flux was related exponentially to O₂ consumption and it outweighed the rate of N₂O production only at >34  °C. Thus, it appears that in the forest soil, where nitrification was the main source of N₂O, temperature affected the N₂O flux less dramatically than in the arable soil, where a temperature increase strongly stimulated N₂O production by enhancing favourable conditions for denitrification. Received: 26 August 1998     

Effects of the nitrification inhibitor nitrapyrin and tillage practices on yield-scaled nitrous oxide emission from a maize field in Iran

Nitrification inhibitors can effectively decrease nitrification rates and nitrous oxide(N₂O)emission while increasing crop yield under certain conditions.However,there is no information available on the effects of nitrification inhibitors and tillage practices on N₂O emissions from maize cropping in Iran.To study how tillage practices and nitrapyrin(a nitrification inhibitor)affect N₂O emission,a split factorial experiment using a completely randomized block design with three replications was carried out in Northeast Iran,which has a cold semiarid climate.Two main plots were created with conventional tillage and minimum tillage levels,and two nitrogen(N)fertilizer(urea)management systems(with and without nitrapyrin application)were created as subplots.Tillage level did not have any significant effect on soil ammonium(NH₄⁺)and nitrate(NO₃^-)concentrations,cumulative amount and yield-scaled N₂O emission,and aboveground biomass of maize,whereas nitrapyrin application showed significant effect.Nitrapyrin application significantly reduced the cumulative amount of N₂O emission by 41%and 32%in conventional tillage and minimum tillage practices,respectively.A reduction in soil NO₃^-concentration by nitrapyrin was also observed.The average yield-scaled N₂O emission was 13.6 g N₂O-N kg^-1N uptake in both tillage systems without nitrapyrin application and was significantly reduced to 7.9 and 8.2 g N₂O-N kg^-1N uptake upon the application of nitrapyrin in minimum tillage and conventional tillage practices,respectively.Additionally,nitrapyrin application increased maize biomass yield by 4%and 13%in the minimum tillage and conventional tillage systems,respectively.Our results indicate that nitrapyrin has a potential role in reducing N₂O emission from agricultural systems where urea fertilizers are broadcasted,which is common in Iran due to the practice of traditional farming.     

Nitrapyrin effectiveness in reducing nitrous oxide emissions decreases at low doses of urea in an Andosol

In the tropics,frequent nitrogen(N)fertilization of grazing areas can potentially increase nitrous oxide(N₂O)emissions.The application of nitrification inhibitors has been reported as an effective management practice for potentially reducing N loss from the soil-plant system and improving N use efficiency(NUE).The aim of this study was to determine the effect of the co-application of nitrapyrin(a nitrification inhibitor,NI)and urea in a tropical Andosol on the behavior of N and the emissions of N₂O from autotrophic and heterotrophic nitrification.A greenhouse experiment was performed using a soil(pH 5.9,organic matter content 78 g kg^-1,and N 5.6 g kg^-1)sown with Cynodon nlemfuensis at 60%water-filled pore space to quantify total N₂O emissions,N₂O derived from fertilizer,soil ammonium(NH₄⁺)and nitrate(NO₃^-),and NUE.The study included treatments that received deionized water only(control,NI).No significant differences were observed in soil NH₄⁺content between the UR and UR+NI treatments,probably because of soil mineralization and NO₃^-produced by heterotrophic nitrification,which is not effectively inhibited by nitrapyrin.After 56 d,N₂O emissions in UR(0.51±0.12 mg N₂O-N concluded that the soil organic N mineralization and heterotrophic nitrification are the main processes of NH₄⁺and NO₃^-production.Additionally,it was found that N₂O emissions were partially a consequence of the direct oxidation of the soil's organic N via heterotrophic nitrification coupled to denitrification.Finally,the results suggest that nitrapyrin would likely exert significant mitigation on N₂O emissions only if a substantial N surplus exists in soils with high organic matter content.     

N2O and NO production in various Chinese agricultural soils by nitrification

Eleven types of agricultural soils were collected from Chinese uplands and paddy fields to compare their N₂O and NO production by nitrification under identical laboratory conditions. Before starting the assays, all air-dried soils were preincubated for 4 weeks at 25 °C and 40% WFPS (water-filled pore space). The nitrification activities of soils were determined by adding (NH₄)₂SO₄ (200 mg N kg⁻¹ soil) and incubating for 3 weeks at 25 °C and 60% WFPS. The net nitrification rates obtained fitted one of two types of models, depending on the soil pH: a zero-order reaction model for acidic soils and one neutral soil (Group 0); or a first-order reaction model for one neutral soil and alkaline soils (Group 1). The results suggest that pH is the most important factor in determining the kinetics of soil nitrification from ammonium. In the Group 1 soils, initial emissions (i.e. during the first week) of N₂O and NO were 82.6 and 83.6%, respectively, of the total emissions during 3 weeks of incubation; in the Group 0 soils, initial emissions of N₂O and NO were 54.7 and 59.9%, respectively, of the total emissions. The net nitrification rate in the first week and second-third weeks were highly correlated with the initial and subsequent emissions (i.e. during the second and third weeks), respectively, of N₂O and NO. The average percentages of emitted (N₂O+NO)-N relative to net nitrification N in initial and subsequent periods were 2.76 and 0.59 for Group 0, and 1.47 and 0.44 for the Group 1, respectively. The initial and subsequent emission ratios of NO/N₂O from Group 0 (acidic) soils were 3.77 and 2.52 times, respectively, higher than those from Group 1 soils (P<0.05).     

Factors influencing nitrous oxide and methane emissions from minerotrophic fens in northeast Germany

 At two field sites representing northeastern German minerotrophic fens (Rhin-Havelluch, a shallow peat site; Gumnitz, a partially drained peat site) the influence of different factors (N fertilization, groundwater table, temperature) on N₂O and CH₄ emissions was investigated. The degraded fens were sources or sinks of the radiatively active trace gases investigated. The gas fluxes measured were much higher than those found in other terrestrical ecosystems such as forests. Lowering the groundwater table increased the release of N₂O and the oxidation of CH₄. High CH₄ emission rates occurred when the groundwater tables and soil temperatures were high (>12  °C). N fertilization stimulated the release of N₂O only when application rates were very high (480 kg N ha^–1). A moderate N supply (60 or 120 kg N ha^–1) hardly increased the release of N₂O in spite of high soluble soil NO₃ ^– contents. Received: 31 October 1997     

N dynamics and sources of N2O production following pig slurry application to a loamy soil

Carbon (C) and Nitrogen dynamics and sources of nitrous oxide (N₂O) production were investigated in a loamy soil amended with pig slurry. Pig slurry (40000kgha^–1) or distilled H₂O was applied to intact soil cores of the upper 5cm of a loamy soil which were incubated under aerobic conditions for 28 days at 25°C. Treatments were with or without acetylene (C₂H₂), which is assumed to inhibit the reduction of N₂O to dinitrogen (N₂), and with or without dicyandiamide (DCD), which is thought to inhibit nitrification. Volatilization of ammonia (NH₃), pH, carbon dioxide (CO₂) and N₂O production, and ammonium (NH₄ ⁺) and nitrate NO₃ ^–) concentrations were monitored. The pH of the pig slurry amended soil increased from an initial value of 7.1 to pH 8.3 within 3 days; it then decreased slowly but was still at a value of 7.4 after 28 days. Twenty percent of the NH₄ ⁺ applied volatilized within 28 days. Sixty percent of the C applied in the pig slurry evolved as CO₂, if no priming effect was assumed, but only 38% evolved when the soil was amended with DCD. Pig slurry significantly increased denitrification and the ratio between its gaseous products, N₂O and N₂, was 0.21. No significant increases in NO₃ ^– concentration occurred, and N₂O produced through nitrification was 0.07mg N₂O-N kg^–1 day^–1 or 33% of the total N₂O produced. C₂H₂ was used as a C substrate by microorganisms and increased the production of N₂O. Received: 12 May 1997     

Influence of 2-chloro-6 (trichloromethyl) pyridine and dicyandiamide on nitrous oxide emission under different soil conditions

Abstract

Two experiments were conducted to evaluate the inhibitory effects of 2-chloro-6 (trichloromethyl) pyridine (nitrapyrin) and dicyandiamide on nitrous oxide (N₂O), a greenhouse gas, emission from soils amended with ammonium sulfate. In the two experiments, samples of an Andosol and a Gray Lowland soil were kept in glass vessels sealed with a butyl rubber cap and incubated at 25°C. In the first experiment, nitrapyrin (1 µg g^?1 dry soil) and dicyandiamide (10 µg g^?1 dry soil) were applied to samples of a water-saturated Andosol and a Gray Lowland soil to which ammonium sulfate had been applied at a rate of 0.1 mg N g^?1 dry soil. Nitrapyrin decreased N₂O emissions from the Andosol and the Gray Lowland soil by 71% and 24%, respectively. Dicyandiamide decreased N₂O emissions from the Andosol and Gray Lowland soil by 31% and 18%, respectively. In the second experiment, nitrapyrin (1 µg g^?1 dry soil) was applied to samples of an Andosol at 51% water-filled pore space to which ammonium sulfate had been applied at rates of 0.01, 0.1 and 0.5 mg N g^?1 dry soil. Nitrapyrin decreased N₂O emissions by 62%, 83% and 74%, respectively. Changes in the NH⁺ ₄ and NO^? ₂ + NO^? ₃ concentrations in soil showed that nitrapyrin and dicyandiamide slowed down the nitrification process, but did not completely stop the process at any time. The results reveal the potential of nitrification inhibitors to decrease N₂O emission from fertilized soil in a wide range of moisture conditions and nitrogen levels.