Variables controlling denitrification from earthworm casts and soil in permanent pastures

Summary Denitrification (using the acetylene block method) was determined in earthworm casts and soils from permanent, drained or undrained pasture plots fertilized with 0 or 200 kg N ha^-1 year^-1 as ammonium nitrate. Rates of N₂O production from soil cores were about three times higher from the fertilized than from the unfertilized plots while drainage had a relatively small effect. Denitrification rates from casts were 3–5 times higher than those from soil irrespective of the drainage treatment. Casts generally had higher NO _inf3 ^sup- , NH _inf4 ^sup+ , and moisture contents, and higher microbial respiration rates than soil. Rates of N₂O production were determined primarily by NO _inf3 ^sup- supply, secondarily by moisture; available C did not appear to limit denitrification in these pastures. Estimates of the potential contribution of casts to denitrification ranges from 10.1% of 29.3 kg ha^-1 year^-1 from the unfertilized, drained plot to 22% of 82.5 kg ha^-1 year^-1 from the fertilized undrained plot.     

Denitrification and nitrogen immobilization as affected by organic matter and different forms of nitrogen added to an anaerobic water-sediment system

The effects of wheat straw and different forms of N on denitrification and N immobilization were studied in an anaerobic water-sediment system. The water-sediment system was supplemented with various combinations of wheat straw and ¹⁵N-labelled and unlabelled (NH₄)₂SO₄ or KNO₃, and incubated anaerobically at 30°C for 10 days. ¹⁵N-labelled and unlabelled NO _inf3 ^sup- , NO _inf2 ^sup- , NH _inf4 ^sup+ , and organic N were determined in the water-sediment system. The gases evolved (N₂, CO₂, N₂O, and CH₄) were analyzed by gas chromatography at regular intervals. Larger quantities of ¹⁵N₂–N and organic ¹⁵N were formed in wheat straw-amended systems than in non-amended systems. Trends in CO₂ production were similar to those of N₂–N evolution. The evolution of N₂O and CH₄ was negligible. Denitrification processes accounted for about 22 and 71% of the added ¹⁵NO _inf3 ^sup- –N in the absence and presence of wheat straw, respectively. The corresponding denitrification rates were 3.4 and 12.4 g ¹⁵Ng^-1 dry sediment day^-1. In systems amended with ¹⁵NO _inf3 ^sup- –N and ¹⁵NO _inf3 ^sup- +NH _inf4 ^sup+ –N without wheat straw, 1.82 and 1.58%, respectively, of the added ¹⁵NH _inf3 ^sup- –N was immobilized. The corresponding figures for the same systems supplemented with wheat straw were 5.08 and 4.10%, respectively. Immobilization of ¹⁵NO _inf4 ^sup+ –N was higher than that of ¹⁵NO _inf3 ^sup- –N. The presence of NO _inf3 ^sup- –N did not stimulate NH _inf4 ^sup+ –N immobilization.     

Effect of bulk density and soil water tension on denitrification in the rhizosphere of spring wheat (Triticum vulgare

Summary Pot experiments were carried out to study the influence of bulk density (D _b), soil water tension (pF) and presence of plants (spring wheat) on denitrification in a low-humus B_t-horizon of a udalf. Pots of only 5-cm depth were found to be most suitable for the experiments when using the acetylene inhibition method. Almost homogeneous soil compaction between 1.1 and 1.6g soil cm^–3 was achieved by a Proctor tamper. Water tensions were adjusted by means of ceramic plates on which negative pressure was applied. No denitrification was detected in unplanted pots. With planted pots and increasing bulk density denitrification increased more in pots with 14-day-old plants than in pots with 7-day-old plants. With 14-day-old plants N₂O emission pot^–1 increased steadily from 2 mol at D _b 1.1 to 8 mol at D _b 1.6, when soil moisture was adjusted to pF 1.5, although root growth was impaired by higher bulk density. From an experiment with different bulk densities and water tensions it could be deduced that the air-filled porosity ultimately determined the rate of denitrification. When low water tension was applied for a longer period, water tension had an overriding effect on total denitrification. Denitrification intensity, however, i.e. the amount of N₂O g^–1 root fresh weight, was highest when low water tension was accompanied by high bulk density. The results suggest that the increase in denitrification intensity at oxygen stress is partly due to higher root exudation.     

Denitrification activity in the root zone of a sludge-amended desert soil

Summary We evaluated potential NO _inf3 ^sup- losses from organic and inorganic N sources applied to improve the growth of cotton (Gossypium hirsutum) on a Pima clay loam soil (Typic Torrifluvent). An initial set of soil cores (April 1989) was collected to a depth of 270 cm from sites in a cotton field previously amended with anaerobically digested sewage sludge or an inorganic N fertilizer. The denitrification potential was estimated in all soil samples by measuring N₂O with gas chromatography. Soils amended with a low or high rate of sludge showed increased denitrification activity over soil samples amended with a low rate or inorganic N fertilizer. All amended samples showed greater denitrification activity than control soils. The denitrification decreased with soil depth in all treatments, and was only evident as deep as 90 cm in the soils treated with the high sludge rate. However, when soils collected from depths greater than 90 cm were amended with a C substrate, significant denitrification activity occurred. These date imply that organisms capable of denitrification were present in all soil samples, even those at depths far beneath the root zone. Hence, denitrification was C-substrate limited. A second series of soil cores taken later in the growing season (July 1989) confirmed these data. Denitrification losses (under laboratory conditions) to a soil depth of 270 cm represented 1–4% of total soil N depending on treatment, when the activity was C-substrate limited. With additional C substrate, the denitrification losses increased to 15–22% of the total soil N.     

Effect of an increasing carbon: nitrate-N ratio on the reliability of acetylene in blocking the N2O-reductase activity of denitrifying bacteria in soil

Summary In model experiments with a silty loam soil the effect of different C : NO _inf3 ^sup- -N ratios on the reliability of C₂H₂ (1% v/v) in blocking N₂O-reductase activity was examined. The soil was carefully mixed with different amounts of powdered lime leaves (Tilia vulgaris) to obtain organic C contents of about 1.8, 2.3, and 2.8%, and of NO _inf3 ^sup- solution to give C : NO _inf3 ^sup- -N ratios of 84, 107, 130, 156, 200, and 243. The soil samples were incubated in specially modified anaerobic jars (22 days, 25°C, 80% water-holding capacity, He atmosphere) and the atmosphere was analysed for N₂, N₂O, CO₂, and C₂H₂ by gas chromatography at regular intervals. Destruction jars were used to analyse soil NO _inf3 ^sup- , NH ₄ ⁺ and C. The results clearly showed that N₂O-reductase activity was completely blocked by 1% (v/v) C₂H₂ only as long as NO _inf3 ^sup- was present. In the presence of C₂H₂, NO _inf3 ^sup- was apparently entirely converted into N₂O. The C₂H₂ blockage of N₂O-reductase activity ceased earlier in soils with a wide C : NO _inf3 ^sup- -N ratio (156, 200, and 243) than in those with closer C : NO _inf3 ^sup- -N ratios (84, 107, and 130). As soon as NO _inf3 ^sup- was exhausted, N₂O was reduced to N₂ in spite of C₂H₂. The wider the C : NO _inf3 ^sup- -N ratio, the earlier the production of N₂ and the less the reliability of the C₂H₂ blockage. In the untreated control complete inhibition of N₂O-reductase activity by C₂H₂ lasted for 7–12 days. In the field, estimates of total denitrification losses by the C₂H₂ inhibition technique should be considered reliable only as long as NO _inf3 ^sup- is present. Consequently, NO _inf3 ^sup- monitoring in the field is essential, particularly in soils supplied with easily decomposable organic matter.     

Microbial biomass,N mineralization,and the activities of various enzymes in relation to nitrate leaching and root distribution in a slurry-amended grassland

High rates of cattle slurry application induce NO _inf3 ^sup- leaching from grassland soils. Therefore, field and lysimeter trials were conducted at Gumpenstein (Austria) to determine the residual effect of various rates of cattle slurry on microbial biomass, N mineralization, activities of soil enzymes, root densities, and N leaching in a grassland soil profile (Orthic Luvisol, sandy silt, pH 6.6). The cattle slurry applications corresponded to rates of 0, 96, 240, and 480 kg N ha^-1. N leaching was estimated in the lysimeter trial from 1981 to 1991. At a depth of 0.50 m, N leaching was elevated in the plot with the highest slurry application. In October 1991, deeper soil layers (0–10, 10–20, 20–30, 30–40, and 40–50 cm) from control and slurry-amended plots (480 kg N ha^-1) were investigated. Soil biological properties decreased with soil depth. N mineralization, nitrification, and enzymes involved in N cycling (protease, deaminase, and urease) were enhanced significantly (P<0.05) at all soil depths of the slurry-amended grassland. High rates of cattle slurry application reduced the weight of root dry matter and changed the root distribution in the different soil layers. In the slurry-amended plots the roots were mainly located in the topsoil (0–10 cm). As a result of this study, low root densities and high N mineralization rates are held to be the main reasons for NO _inf3 ^sup- leaching after heavy slurry applications on grassland.     

Influence of thiosulfate on nitrification,denitrification, and production of nitric oxide and nitrous oxide in soil

Thiosulfate and CS₂ inhibit nitrification. The effect of the addition of thiosulfate on the turnover of inorganic N compounds was tested in an Egyptian and a German arable soil under nitrifying and denitrifying conditions. For nitrification, the soils were amended with NH _inf4 ^sup+ and incubated under aerobic conditions. For denitrification, the soils were amended with NO _inf3 ^sup- and incubated under anaerobic conditions. In both cases, the thiosulfate decreased with time while tetrathionate accumulated to an intermediate extent. Both compounds disappeared completely after <25 days. Production of CS₂ was not observed. Carbonyl sulfide was produced only in the Egyptian soil, but production decreased with increasing amounts of added thiosulfate. Under nitrifying conditions, the addition of increasing amounts of thiosulfate (25, 50, and 100 g S g^-1 dry weight) resulted in decreasing rates of NH _inf4 ^sup+ oxidation to NO _inf3 ^sup- ; it also resulted in an increasing intermediate accumulation of NO _inf2 ^sup- and NO, and in an increasing production of N₂O. Under denitrifying conditions, the addition of increasing amounts of thiosulfate did not significantly affect the rate of NO _inf3 ^sup- reduction, and resulted in an increasing intermediate accumulation of NO _inf2 ^sup- and of NO only in the German soil in which the production of N₂O was slightly inhibited by thiosulfate. These results demonstrate that the nitrification of NH _inf4 ^sup+ and NO _inf2 ^sup- was inhibited by increasing concentrations of thiosulfate and/or tetrathionate without involving the formation of volatile S compounds as potential nitrification inhibitors. Denitrification was not affected by the addition of thiosulfate.     

Denitrification under different cultivated plants: effects of soil moisture tension,nitrate concentration,and photosynthetic activity

Summary Plant effects on the denitrification rate were investigated in pot experiments at different soil moisture tensions and nitrate concentrations. Nitrate concentrations and the soil moisture tension were regulated immediately before each measurement. The effects of the plants on denitrification rates were dependent on the soil moisture tension. At a low soil moisture tension (–7 cm H₂O), there was a 10-fold increase in the denitrification rate (planted versus unplanted soil). At a medium moisture tension (–30 cm H₂O) the plants had practically no effect, and at the highest tension (–60 cm H₂O) the effect was slightly negative. Large differences in denitrification rates under different plant species were observed. At a low soil moisture tension, the average denitrification rate (g N kg^–1 soil h^–1) was 39–42 under small grains (barley, wheat, and oats), 47–82 under the grasses (cocksfoot, meadow grass, meadow fescue, and timothy) and 18 under red clover. The differences between the monocots were attributable to differences in plant growth rates, rather than to any specific difference in stimulation or inhibition of denitrification, since the variations in photosynthetic activity fairly well predicted the differences in denitrification rates under different monocots. Clover, however, gave much lower denitrification rates than those predicted by the photosynthetic activity.     

Effects of vegetation regime on denitrification potential in two tropical volcanic soils

Effects of vegetation and nutrient availability on potentail denitrification rates were studied in two volcanic, alluvial-terrace soils in lowland Costa Rica that differ greatly in weathering stage and thus in availability of P and base cations. Potential denitrification rates were significantly higher in plots where vegetation had been left undisturbed than in plots where all vegetation had been removed continuously, and were higher on the less fertile of the two soils. The potential denitrification rates were correlated strongly with respiration rates, levels of mineralizable N, microbial biomass, and moisture content, and moderately well with concentrations of extractable NH _inf4 ^sup+ , Kjeldahl N, and total C. In all plots, denitrification rates were stimulated by the removal of O₂ and by the addition of glucose but not by the addition of water or NO _inf3 ^sup- .This is Paper 2772 of the Forest Research Laboratory, Oregon State University     

Increase in nitrous oxide production in soil induced by ammonium and organic carbon

We observed that soil cores collected in the field containing relatively high NH _inf4 ^sup+ and C substrate levels produced relatively large quantities of N₂O. A series of laboratory experiments confirmed that the addition of NH _inf4 ^sup+ and glucose to soil increase N₂O production under aerobic conditions. Denitrifying enzyme activity was also increased by the addition of NH _inf4 ^sup+ and glucose. Furthermore, NH _inf4 ^sup+ and glocose additions increased the production of N₂O in the presence of C₂H₂. Therefore, we concluded that denitrification was the most likely source of N₂O production. Denitrification was not, however, directly affected by NH _inf4 ^sup+ in anaerobic soil slurries, although the use of C substrate increased. In the presence of a high substrate C concentration, N₂O production by denitrifiers may be affected by NO _inf3 ^sup- supplied from NH _inf4 ^sup+ through nitrification. Alternatively, N₂O may be produced during mixotrophic and heterotrophic growth of nitrifiers. The results indicated that the NH _inf4 ^sup+ concentration, in addition to NO _inf3 ^sup- , C substrate, and O₂ concentrations, is important for predicting N₂O production and denitrification under field conditions.     

Denitrification,N2-fixation and fermentation during anaerobic incubation of soils amended with glucose and nitrate

Nitrate and glucose additions were investigated for their role in the C and N dynamics during anaerobic incubation of soil. A gas-flow soil core method was used, in which the net production of N₂, N₂O, NO, CO₂, and CH₄ under a He atmosphere could be monitored both accurately and frequently. In all experiments clayey silt loam soil samples were incubated for 9 days at 25 °C. Addition of nitrate (50 mg KNO₃-N kg^-1 soil) had no effect on total denitrification and CO₂ production rates, while the N₂O/N₂ ratio was affected considerably. The cumulative N₂O production exceeded the cumulative N₂ production for 6 days in the treatment with nitrate addition, compared to 1.2 days in the unamended treatment. Glucose addition stimulated the microbial activity considerably. The denitrification rates were limited by the growth rate of the denitrifying population. During denitrification no significant differences were observed between the treatments with 700 mg glucose-C kg^-1 and 4200 mg glucose-C kg^-1, both in combination with 50 mg KNO₃-N kg^-1. The N₂ production rates were remarkably low, until NO _inf3 ^sup- exhaustion caused rapid reduction of N₂O to N₂ at day 2. During the denitrification period 15–18 mg N kg^-1 was immobilised in the growing biomass. After NO _inf3 ^sup- shortage, a second microbial population, capable of N₂-fixation, became increasingly important. This change was clearly reflected in the CO₂ production rates. Net volatile fatty acid (VFA) production was monitored during the net N₂-fixation period with acetate as the dominant product. N₂-fixation faded out, probably due to N₂ shortage, followed by increased VFA production. In the high C treatment butyrate became the most important VFA, while in the low C treatment acetate and butyrate were produced at equal rates. During denitrification no VFA accumulation occurred; this does not prove, however, that denitrification and fermentation appeared sequentially. The experiments illustrate clearly the interactions of C-availability, microbial population and nitrate availability as influencing factors on denitrification and fermentation.Dedicated to Professor J. C. G. Ottow on the occasion of his 60th birthday     

Evaluation of denitrification losses by the acetylene inhibition technique in a permanent ryegrass field (Lolium perenne L.) fertilized with animal slurry or ammonium nitrate

In a field experiment, the effect of animal slurry, (with and without the nitrification inhibitor dicyandiamide on total denitrification losses estimated by the C₂H₂ inhibition technique was measured over 2 years (1989–1990). During this period, four different plots (each with four replicates) were fertilized six times with 150 kg N ha^-1 in the form of cattle-pig slurry or NH₄NO₃. Soil samples (0–20 cm) were analysed at regular intervals for NH _inf4 ^sup+ and NO _inf3 ^sup– concentrations. The soil water content was determined gravimetrically. During the first year (1989) total denitrification losses from unfertilized, mineral-fertilized, and animal slurry-amended plots (with or without dicyandiamide) were estimated as 0.2, 3.1, 0.7, and 0.6 kg N ha^-1, respectively. During the second year (1990) the denitrification losses were 0.4, 1.3, 0.7, and 0.7 kg N ha^-1, respectively. There was a clear relationship between the NO _inf3 ^sup– concentration or soil water content and the denitrification rate. The results are siteund experiment-specific and cannot be generalized so far.     

Nitrate alters the flavonoid profile and nodulation in pea (Pisum sativum L.)

A rhizosphere application of NO _inf3 ^sup- and/or naringenin affected the Pisum sativum — Rhizobium leguminosarum biovar viciae symbiosis. NO _inf3 ^sup- (5 mM) lowered while naringenin raised the nodulation status (nodule numbers and weight) and nodule efficiency (C₂H₂ reduction activity). However, the inhibitory effect of NO _inf3 ^sup- was to some extent alleviated when applied in combination with naringenin. The plant biomass was increased by the application of NO _inf3 ^sup- and naringenin, either alone or in combination, while a higher root: shoot ratio was observed only in the naringenin-treated plants. Root flavonoids are known to regulate the expression of nod genes; their high-performance liquid chromatography profile was influenced in different ways by NO _inf3 ^sup- and naringenin.     

Denitrifikationsverluste eines gemüsebaulich genutzten Bodens in Abhängigkeit von der mineralischen N-Düngung

Denitrification losses from a horticultural soil as affected by mineral N-fertilization To investigate denitrification in the A_p-horizon from a horticultural cambisol as affected by mineral N-fertilization, measurements of N₂O-release from the soil surface and N₂O-production in the upper 10 cm soil layer were carried out. The acetylene inhibition technique was used. The loamy sand was amended with 86 and 186 kg N·ha^?1 (ammonium nitratecalcium carbonate mixture). The field was cropped with celeriac (Apium graveolens L. var. rapaceum). Denitrification rates as well as soil temperature, moisture, nitrate and watersoluble carbon were measured from mid July until the end of October. In both N treatments denitrification rates were low, but higher rates could be measured in the higher N-treatment. They reached amounts of 0.6 to 134.3 g N₂O-N·ha^?1day^?1. Estimated N-loss by denitrification totalled about 3.5 in the low and 4.9 kg N·ha^?1 in the high N-treatment for the whole sampling period (107 days). Spatial variability of denitrification rates was high (39–283%). The relationship between soil temperature, moisture, nitrate content as well as watersoluble carbon and denitrification rate was shown by regression analysis.     

Immobilization of ammonium and nitrate and their interaction with native N in three Illinois Mollisols

Summary Three Illinois Mollisols were incubated for 2 weeks at 25°C after treatment with different amounts of glucose and/or ¹⁵N-labelled (NH₄)₂SO₄ or ¹⁵N-labelled KNO₃. The objectives were: (1) to compare the immobilization and interaction of NH _inf4 ^sup+ –N and NO _inf3 ^sup- –N with the native soil N, and (2) to study the relationship between immobilization of applied N and the added N interaction. As determined, immobilized N refers to forms not extractable with 2 MKCl (immobilized ¹⁵N+clay-fixed ¹⁵NH _inf4 ^sup+ ). In all cases, both NH _inf4 ^sup+ –N and NO _inf3 ^sup- –N were actively immobilized and transformed into organic forms in the presence of glucose. In the absence of glucose, a higher proportion of NH _inf4 ^sup+ than NO _inf3 ^sup- was recovered in organic forms. Although the three soils differed considerably in the amounts of applied N immobilized, similar trends in N immobilization were observed. A positive added N interaction occurred with all soils, the magnitude increasing with the rate of N addition. In the absence of glucose, higher added N interactions were obtained for NH _inf4 ^sup+ than NO _inf3 ^sup- , whereas there was very little difference between NH _inf4 ^sup+ and NO _inf3 ^sup- in the presence of glucose. The results indicate that under conditions of rapid immobilization (e.g., in the presence of glucose), NH _inf4 ^sup+ and NO _inf3 ^sup- will show comparable interaction with the native soil N, whereas in unamended soil, the extent of this interaction will be greater with NH _inf4 ^sup+ than with NO _inf3 ^sup- . Significant correlations were observed between applied N immobilized and the added N interaction only in one soil having a high initial mineral N content.     

Seasonal pattern of denitrification under an irrigated wheat-maize cropping system fertilized with urea and farmyard manure in different combinations

Under semiarid subtropical field conditions, denitrification was measured from the arable soil layer of an irrigated wheat–maize cropping system fertilized with urea at 50 or 100 kg N ha^–1 year^–1 (U₅₀ and U₁₀₀, respectively), each applied in combination with 8 or 16 t ha^–1 year^–1 of farmyard manure (FYM) (F₈ and F₁₆, respectively). Denitrification was measured by acetylene inhibition/soil core incubation method, also taking into account the N₂O entrapped in soil cores. Denitrification loss ranged from 3.7 to 5.7 kg N ha^–1 during the growing season of wheat (150 days) and from 14.0 to 30.3 kg N ha^–1 during the maize season (60 days). Most (up to 61%) of the loss occurred in a relatively short spell, after the presowing irrigation to maize, when the soil temperature was high and a considerable NO₃^–-N had accumulated during the preceding 4-month fallow; during this irrigation cycle, the lowest denitrification rate was observed in the treatment receiving highest N input (U₁₀₀+F₁₆), mainly because of the lowest soil respiration rate. Data on soil respiration and denitrification potential revealed that by increasing the mineral N application rate, the organic matter decomposition was accelerated during the wheat-growing season, leaving a lower amount of available C during the following maize season. Denitrification was affected by soil moisture and by soil temperature, the influence of which was either direct, or indirect by controlling the NO₃^– availability and aerobic soil respiration. Results indicated a substantial denitrification loss from the irrigated wheat–maize cropping system under semiarid subtropical conditions, signifying the need of appropriate fertilizer management practices to reduce this loss.     

Effects of ammonium and nitrate on the growth of vesicular-arbuscular mycorrhizalErythrina poeppigiana O.I. Cook seedlings

Erythrina poeppigiana, a woody tropical plant, was inoculated with vesicular-arbuscular mycorrhizal (VAM) fungiGlomus etunicatum Becker and Gerdeman,G. mosseae Nicol. and Gerd. Gerdeman and Trappe, orG. intraradices Schenk and Smith. Growth, N uptake, and nutrition were evaluated in VAM-inoculated plants and controls fertilized with two levels (3 or 6 mM) of either NH _inf4 ^sup+ -N or NO _inf3 ^sup- -N. The response by the mycorrhizal plants to N fertilization, according to N source and/or level differed significantly from that of the control plants. In general, the growth of the mycorrhizal plants was similar to that of the non-mycorrhizal plants when N was provided as NH _inf4 ^sup+ . When the N source was NO _inf3 ^sup- the control plants grew significantly less than the VAM plants. Inoculation with VAM fungi gave yield increases of 255 and 268% forG. etunicatum-colonized plants, 201 and 164% forG. mosseae-colonized plants and 286 and 218% forG. intraradices-colonized plants fertilized with 3 and 6 mM NO _inf3 ^sup- -N, respectively. The increased growth and acquisition of nutrients by plants fertilized with NO _inf3 ^sup- -N and inoculated with VAM shows that VAM mycelium has a capacity for NO _inf3 ^sup- absorption. The results also showed thatE. poeppigiana seedlings preferred NH _inf4 ^sup+ as an N source.G. etunicatum was the most effective endophyte, not only increasing N, P, Ca, Mg, and Zn uptake in the presence of NO _inf3 ^sup- fertilizer but also P and Mg in the presence of NH _inf4 ^sup+ applications. From these results we conclude that VAM symbiosis affects N metabolism inE. poeppigiana plants and that this species can overcome limitations on the use of NO _inf3 ^sup- -N by the mediation of VAM fungi.     

Influence of oxygen on denitrification and aerobic respiration in soil

Summary The influence of the partial pressure of oxygen on denitrification and aerobic respiration was investigated at defined P02 values in a mull rendzina soil. The highest denitrification and respiration rates obtained in remoistened, glucose- and nitrate-amended soil were 43 1 N₂0 h^–1g^–1 soil and 130 1 O₂ h^–1g^–1 soil, respectively. At -55 kPa matric water potential, corresponding to 40% water saturation, N₂0 was produced only below P0₂ 40 hPa. The K _m, for O₂ was 3.0 x 10^–6 M. Formation of N₂O and consumption of O₂ occurred simultaneously with half maximum rates at P0₂ 6.7–13.3 hPa. Nitrite accumulated in soil below 40 hPa and increased with decreasing pO₂. The upper threshold for N₂0 formation in amended soil was P0₂ 33–40 hPa (39-47 M O₂).     

Denitrification in the rooting zone of cropped soils with regard to methodology and climate: A review

Summary Denitrification N losses can be determined by three methods. The first is by estimating the non-recovery of ¹⁵ N-labelled compounds (¹⁵N-balance method). Using this method, denitrification losses are deduced from the balance of an N budged (¹⁵N-labeled fertilizer), having accounted for transformations in soil, plant uptake, and leaching losses. The evolution of gaseous N from native soil N is not taken into account by this procedure. Studies on arable land with annual crops in the temperate zone have shown that of the fertilizer N applied, about 20–500% (10–70 kg N^* ha^–1) is not recovered at the end of the growth period. The second method of determining denitrification N losses is by in situ field measurement of ¹⁵ N ₂ and ¹⁵ N ₂ O production. Under this procedure, ¹⁵N-enriched N is applied to a plot and the denitrification N losses are determined by covering the soil. The method allows a quantitative estimate of the relative contributions to the emitted gas by both the original enriched source and the native soil N. N-evolution rates measured on arable land under a temperate climate are approximately the same order of magnitude as the N losses estimated by the non-recovery of ¹⁵ N method. The third measuring procedure is based on the acetylene inhibition phenomenon. This principle uses the inhibition of bacterial N₂O reduction to N₂ in the presence of acetylene (C₂H₂). The methoddetermines the denitrification of all NO₃ ^–-N irrespective of its source. Measurements on classical crop production systems show maximum N losses in the temperate climate of about 20–30 kg N^* ha^–1 during the growth period of annual crops. A similar level of denitrification is estimated for grassland sites under the same climate. In the subtropics (mediterranean climate with hot summers and mild winters), from both intensively cultivated arable land and grassland sites, N losses may exceed 200 kg^* ha^–1 year^–1. Without the use of irrigation the denitrification flux is negligible in spite of the high temperatures in this climate.     

The utility of process-based models for simulating N2O emissions from soils: A case study based on Costa Rican coffee plantations

Soil moisture and gaseous N-flux (N₂O, N₂) dynamics in Costa Rican coffee plantations were successively simulated using a mechanistic model (PASTIS) and two process-based models (NGAS and NOE). Two fertilized (250 kg N ha⁻¹ y⁻¹) coffee plantations were considered, namely a monoculture and a system shaded by the N₂ fixing legume species Inga densiflora. In situ N₂O fluxes were previously measured in these plantations. NGAS and NOE used specific microbial activities for the soils. To parameterize NGAS, we estimated N mineralization via in situ incubations and the contribution of heterotrophic soil respiration to total soil respiration. Potential denitrification rates and the proportion of denitrified N emitted as N₂O were measured in the laboratory to define the values of NOE parameters, as well as nitrification rates and related N₂O production rates for parameterizing both models. Soil moisture and both NGAS and NOE N₂O fluxes were best modelled on an hourly time step. Soil moisture dynamics were satisfactorily simulated by PASTIS. Simulated N₂O fluxes by both NGAS and NOE (3.2 and 2.1 kg N ha⁻¹ y⁻¹ for NGAS; 7.1 and 3.7 kg N ha⁻¹ y⁻¹ for NOE, for the monoculture and shaded plantations respectively) were within a factor of about 2 of the observed annual fluxes (4.3 and 5.8 kg N ha⁻¹ y⁻¹, for the monoculture and shaded plantations respectively). Statistical indicators of association and coincidence between simulated and measured values were satisfactory for both models. Nevertheless, the two models differed greatly in describing the nitrification and denitrification processes. Some of the algorithms in the model NGAS were apparently not applicable to these tropical acidic Andosols. Therefore, more detailed information about microbial processes in different agroecosystems would be needed, notably if process-oriented models were to be used for testing strategies for mitigating N₂O emissions.