DENITRIFICATION IN A VERY ACID TROPICAL SOIL

In a very acid upland clay surface soil and with glucose added to give initial C/N weight ratios (added glucose-C: NO₃-N) in the soil of 0, 2 and 5, the rates of evolution of N₂ and N₂O were maximum at C/N = 2 but were significantly less at 0 and 5. The total N₂ and N₂O production was highest at C/N = 0, confirming that increasing amounts of glucose immobilised more nitrate into the biomass. As with added NO^?₃-N, the time lag, preceding a maximum ‘steady state’ rate of N₂0 evolution, increased regularly with increasing glucose. Within this ‘steady state’ period, the gaseous CO₂-C/(N₂+ N₂O)-N weight ratio in the effluent gas are between 1.0 and 1.3, which corresponds well with the stoichiometric ratios of 1.07 and 1.29 for the reduction of NO^?₃ to N₂O and N₂ respectively. Before and after this period, this gaseous C/N ratio was much higher. Denitrification was not observed in subsurface soil even after adding 100 mg kg^?1glucose-C although it contained 4 times as much indigenous nitrate as the surface soil. Inoculating this soil with increasing amounts of the surface soil, up to 15 per cent by weight, induced substantial increases in the rates and amounts of denitrification. The effects of increasing the soil pH. of introducing increasing oxygen concentrations in the influent gas. and the fate of added NH⁺₄-N, are briefly reported here. In these experiments. NO^?₂-N did not accumulate in the incubated soil nor was there any NH₃in the effluent gas. Evolution of N₂ only occurred when N₂O evolution was in its final stages.     

Comparison of two versions of the acetylene inhibition/soil core method for measuring denitrification loss from an irrigated wheat field

 Two versions of the acetylene inhibition (AI)/soil core method were compared for the measurement of denitrification loss from an irrigated wheat field receiving urea-N at a rate of 100 kg ha^–1. With AI/soil core method A, the denitrification rate was measured by analysing the headspace N₂O, followed by estimation of N₂O dissolved in the solution phase using Bunsen absorption coefficients. With AI/soil core method B, N₂O entrapped in the soil was measured in addition to that released from soil cores into the headspace of incubation vessels. In addition, the two methods were also compared for measurement of the soil respiration rate. Of the total N₂O produced, 6–77% (average 40%) remained entrapped in the soil, whereas for CO₂, the corresponding figures ranged from 12–65% (average 44%). The amount of the entrapped N₂O was significantly correlated with the water-filled pore space (WFPS) and with the N₂O concentration in the headspace, whereas CO₂ entrapment was dependent on the headspace CO₂ concentration but not on the WFPS. Due to the entrapment of N₂O and CO₂ in soil, the denitrification rate on several (18 of the 41) sampling dates, and soil respiration rate on almost all (27 of the 30) sampling dates were significantly higher with method B compared to method A. Averaged across sampling dates, the denitrification rate measured with method B (0.30 kg N ha^–1 day^–1) was twice the rate measured with method A, whereas the soil respiration rate measured with method B (34.9 kg C ha^–1 day^–1) was 1.6 times the rate measured with method A. Results of this study suggest that the N₂O and CO₂ entrapped in soil should also be measured to ensure the recovery of the gaseous products of denitrification by the soil core method. Received: 12 May 1998     

Rapid shift from denitrification to nitrification in soil after biogas residue application as indicated by nitrous oxide isotopomers

Nitrous oxide (N₂O) is one of the major greenhouse gases emitted from soils, where it is mainly produced by nitrification and denitrification. It is well known that rates of N₂O release from soils are mainly determined by the availability of substrates and oxygen, but N₂O source apportioning, highly needed to advance N₂O mitigation strategies, still remains challenging. In this study, using an automated soil incubation system, the N₂O site preference, i.e. the intramolecular ¹⁵N distribution, was analyzed to evaluate the progression in N₂O source processes following organic soil amendment. Biogas fermentation residue (BGR; originating from food waste fermentation) was applied to repacked grassland soil cores and compared to ammonium sulfate (AS) application, both at rates equivalent to 160 kg NH₄⁺-N ha⁻¹, and to unamended soil (control). The soil cores were incubated in a helium-oxygen atmosphere with 20 kPa O₂ for 43 days at 80% water-filled pore space. 43-day cumulative N₂O emissions were highest with BGR treated soil accounting for about 1.68 kg N₂O-N ha⁻¹ while application of AS caused much lower fluxes of c. 0.23 kg N₂O-N ha⁻¹. Also, after BGR application, carbon dioxide (CO₂) fluxes showed a pronounced initial peak with steep decline until day 21 whereas with ammonium addition they remained at the background level. N₂O dual isotope and isotopomer analysis of gas samples collected from BGR treated soil indicated bacterial denitrification to be the main N₂O generating process during the first three weeks when high CO₂ fluxes signified high carbon availability. In contrast, in the second half after all added labile carbon substrates had been consumed, nitrification, i.e. the generation of N₂O via oxidation of hydroxylamine, gained in importance reaching roughly the same N₂O production rate compared to bacterial denitrification as indicated by N₂O SP. Overall in this study, bacterial denitrification seemed to be the main N₂O forming process after application of biogas residues and fluxes were mainly driven by available organic carbon.     

Nitrous oxide emission derived from soil organic matter decomposition from tropical agricultural peat soil in central Kalimantan,Indonesia

Our previous research showed large amounts of nitrous oxide (N₂O) emission (>200?kg?N?ha^?1?year^?1) from agricultural peat soil. In this study, we investigated the factors influencing relatively large N₂O fluxes and the source of nitrogen (N) substrate for N₂O in a tropical peatland in central Kalimantan, Indonesia. Using a static chamber method, N₂O and carbon dioxide (CO₂) fluxes were measured in three conventionally cultivated croplands (conventional), an unplanted and unfertilized bare treatment (bare) in each cropland, and unfertilized grassland over a three-year period. Based on the difference in N₂O emission from two treatments, contribution of the N source for N₂O was calculated. Nitrous oxide concentrations at five depths (5–80?cm) were also measured for calculating net N₂O production in soil. Annual N fertilizer application rates in the croplands ranged from 472 to 1607?kg?N?ha^?1?year^?1. There were no significant differences in between N₂O fluxes in the two treatments at each site. Annual N₂O emission in conventional and bare treatments varied from 10.9 to 698 and 6.55 to 858?kg?N?ha^?1?year^?1, respectively. However, there was also no significant difference between annual N₂O emissions in the two treatments at each site. This suggests most of the emitted N₂O was derived from the decomposition of peat. There were significant positive correlations between N₂O and CO₂ fluxes in bare treatment in two croplands where N₂O flux was higher than at another cropland. Nitrous oxide concentration distribution in soil measured in the conventional treatment showed that N₂O was mainly produced in the surface soil down to 15?cm in the soil. The logarithmic value of the ratio of N₂O flux and nitrate concentration was positively correlated with water filled pore space (WEPS). These results suggest that large N₂O emission in agricultural tropical peatland was caused by denitrification with high decomposition of peat. In addition, N₂O was mainly produced by denitrification at high range of WFPS in surface soil.     

Above and Below Ground Measurements of Greenhouse Gases from Swine Effluent Amended Soil

Abstract

As a means of economic disposal and to reduce need for chemical fertilizer, waste generated from swine production is often applied to agricultural land. However, there remain many environmental concerns about this practice. Two such concerns, contribution to the greenhouse effect and stratospheric ozone depletion by gases emitted from waste‐amended soils, have not been thoroughly investigated. An intact core study at Auburn University (32 36′N, 85 36′W) was conducted to determine the source‐sink relationship of three greenhouse gases in three Alabama soils (Black Belt, Coastal Plain, and Appalachian Plateau regions) amended with swine waste effluent. Soil cores were arranged in a completely random design, and treatments used for each soil type consisted of a control, a swine effluent amendment (112 kg N ha^?1), and an ammonium nitrate (NH₄NO₃) fertilizer amendment (112 kg N ha^?1). During a 2‐year period, a closed‐chamber technique was used to determine rates of emission of nitrous oxide (N₂O)–nitrogen (N), carbon dioxide (CO₂)–carbon (C), and methane (CH₄)–C from the soil surface. Gas probes inserted into the soil cores were used to determine concentrations of N₂O‐N and CO₂‐C from depths of 5, 15, and 25 cm. Soil water was collected from each depth using microlysimeters at the time of gas collection to determine soil‐solution N status. Application of swine effluent had an immediate effect on emissions of N₂O‐N, CO₂‐C, and CH₄‐C from all soil textures. However, greatest cumulative emissions and highest peak rates of emission of all three trace gases, directly following effluent applications, were most commonly observed from sandier textured Coastal Plain and Appalachian Plateau soils, as compared to heavier textured Black Belt soil. When considering greenhouse gas emission potential, soil type should be a determining factor for selection of swine effluent waste disposal sites in Alabama.     

Nitrous Oxide Emissions from a Coal Mine Land Reclaimed with Stabilized Manure

Mine‐soil treatment using stabilized manure rapidly sequesters large quantities of organic carbon and nutrients. However, the nutrient‐rich soil conditions may become highly conducive for production and emission of N₂O. We examined this possibility in a Pennsylvania coal mine restored using poultry manure stabilized in two forms: composted (Comp) or mixed with paper mill sludge (Man + PMS) at C/N ratios of 14, 21, and 28 and compared those with the emissions from conventionally treated soil. The mine soil was extremely well drained with 59% coarse fragments. Soil–atmosphere exchange of N₂O and CO₂ was determined using a sampling campaign of ten measurements between 16 June and 14 September 2009 (90 days) and 13 measurements between 28 June and 9 November 2010 (134 days) using static vented chambers at ambient and increased moisture (water added) content. Potential denitrification was determined in a laboratory incubation experiment. While non‐amended mine soil did not have a measurable potential for denitrifying activity, the manure‐based amendments introduced the potential. Soil water filled pore space was less than 60% on most sampling days in both ambient and water‐added plots. Daily N₂O‐N emissions ranged between 40 and 70 g N ha⁻¹ with cumulative emissions of 2–4 kg N ha⁻¹ from non‐amended, lime and fertilizer (L + F) and Comp, and 3–10 kg N ha⁻¹ from Man + PMS treatments. The maximum emission obtained from Man + PMS represented <1% loss of applied N. Although stabilized manure‐treated soil exhibits the potential for N₂O production, the emission is limited when soils are excessively well drained and reducing conditions rarely develop. Copyright © 2015 John Wiley & Sons, Ltd.     

Nitrogen oxides emission from soils bearing a potato crop as influenced by fertilization with treated pig slurries and composts

Nitrous oxide, nitric oxide and denitrification losses from an irrigated soil amended with organic fertilizers with different soluble organic carbon fractions and ammonium contents were studied in a field study covering the growing season of potato (Solanum tuberosum). Untreated pig slurry (IPS) with and without the nitrification inhibitor dicyandiamide (DCD), digested thin fraction of pig slurry (DTP), composted solid fraction of pig slurry (CP) and composted municipal solid waste (MSW) mixed with urea were applied at a rate of 175 kg available N ha⁻¹, and emissions were compared with those from urea (U) and a control treatment without any added N fertilizer (Control). The cumulative denitrification losses correlated significantly with the soluble carbohydrates, dissolved N and total C added. Added dissolved organic C (DOC) and dissolved N affected the N₂O/N₂ ratio, and a lower ratio was observed for organic fertilizers than from urea or unfertilized controls. The proportion of N₂O produced from nitrification was higher from urea than from organic fertilizers. Accumulated N₂O losses during the crop season ranged from 3.69 to 7.31 kg N₂O-N ha⁻¹ for control and urea, respectively, whereas NO losses ranged from 0.005 to 0.24 kg NO-N ha⁻¹, respectively. Digested thin fraction of pig slurry compared to IPS mitigated the total N₂O emission by 48% and the denitrification rate by 33%, but did not influence NO emissions. Composted pig slurry compared to untreated pig slurry increased the N₂O emission by 40% and NO emission by 55%, but reduced the denitrification losses (34%). DCD partially inhibited nitrification rates and reduced N₂O and NO emissions from pig slurry by at least 83% and 77%, respectively. MSW+U, with a C:N ratio higher than that of the composted pig slurry, produced the largest denitrification losses (33.3 kg N ha⁻¹), although N₂O and NO emissions were lower than for the U and CP treatments.This work has shown that for an irrigated clay loam soil additions of treated organic fertilizers can mitigate the emissions of the atmospheric pollutants NO and N₂O in comparison with urea.     

Nitrous oxide emissions from an irrigated sandy-clay loam cropped to maize and wheat

 Nitrous oxide (N₂O) emissions were measured from an irrigated sandy-clay loam cropped to maize and wheat, each receiving urea at 100 kg N ha^–1. During the maize season (24 August–26 October), N₂O emissions ranged between –0.94 and 1.53 g N ha^–1 h^–1 with peaks during different irrigation cycles (four) ranging between 0.08 and 1.53 g N ha^–1 h^–1. N₂O sink activity during the maize season was recorded on 10 of the 29 sampling occasions and ranged between 0.18 and 0.94 g N ha^–1 h^–1. N₂O emissions during the wheat season (22 November–20 April) varied between –0.85 and 3.27 g N ha^–1 h^–1, whereas peaks during different irrigation cycles (six) were in the range of 0.05–3.27 g N ha^–1 h^–1. N₂O sink activity was recorded on 14 of the 41 samplings during the wheat season and ranged between 0.01 and 0.87 g N ha^–1 h^–1. Total N₂O emissions were 0.16 and 0.49 kg N ha^–1, whereas the total N₂O sink activity was 0.04 and 0.06 kg N ha^–1 during the maize and wheat seasons, respectively. N₂O emissions under maize were significantly correlated with denitrification rate and soil NO₃ ^–-N but not with soil NH₄ ⁺-N or soil temperature. Under wheat, however, N₂O emissions showed a strong correlation with soil NH₄ ⁺-N, soil NO₃ ^–-N and soil temperature but not with the denitrification rate. Under either crop, N₂O emissions did not show a significant relationship with water-filled pore space or soil respiration. Received: 11 June 1997     

Modelling soil compaction impacts on nitrous oxide emissions in arable fields

Nitrous oxide (N₂O) emissions comprise the major share of agriculture's contribution to greenhouse gases; however, our understanding of what is actually happening in the field remains incomplete, especially concerning the multiple interactions between agricultural practices and N₂O emissions. Soil compaction induces major changes in the soil structure and the key variables controlling N₂O emissions. Our objective was to analyse the ability of a process‐based model (Nitrous Oxide Emissions (NOE)) to simulate the impact of soil compaction on N₂O emission kinetics obtained from field experiments. We used automatic chambers to continuously monitor N₂O and CO₂ emissions on uncompacted and compacted areas in sugar beet fields during 2 years. Soil compaction led to smaller CO₂ emissions and larger N₂O emissions by inducing anoxic conditions favourable for denitrification. Cumulative N₂O emissions during the crop cycles were 944 and 977 g N ha⁻¹ in uncompacted plots and 1448 and 1382 g N ha⁻¹ in compacted plots in 2007 and 2008, respectively. The NOE model ( Hénault et al., 2005 ) simulated 106 and 138 g N₂O‐N ha⁻¹ in uncompacted plots and 1550 and 650 g N₂O‐N ha⁻¹ in compacted plots in 2007 and 2008, respectively, markedly under‐estimating the nitrification rates and associated N₂O emissions. We modified the model on the basis of published results in order to better simulate nitrification and account for varying N₂O fractions of total end‐products in response to varying soil water and nitrate contents. The modified model (NOE2) better predicted nitrification rates and N₂O emissions following fertilizer addition. Using a fine vertical separation of soil layers of configurable, but constant, thickness (1 cm) also improved the simulations. NOE2 predicted 428 and 416 g N‐N₂O ha⁻¹ in uncompacted plots and 1559 and 1032 g N‐ N₂O ha⁻¹ in compacted plots in 2007 and 2008, respectively. These results show that a simple process‐based model can be used to predict successfully the post‐fertilizer addition kinetics of N₂O emissions and the impact of soil compaction on these emissions. However, large emissions later on during the cropping cycle were not captured by the model, emphasizing the need for further research.     

Greenhouse Gas Emissions following Conversion of a Reclaimed Minesoil to Bioenergy Crop Production

This study provides a comparative assessment of greenhouse gas (GHG) emissions when converting a reclaimed minesoil that was previously under meadow to miscanthus (Miscanthus  × giganteus ) and maize (Zea mays L.) land uses in Ohio, USA. Additionally, effluent from an anaerobic digester at rates of 0, 75, 150, and 225 kg N ha⁻¹ rates was also assessed for C and nutrient fertilization. Results from the study show that land use conversion to maize had the highest net release of GHG equivalent of 6·6 Mg CO_2equ ha⁻¹ y⁻¹, on average, across effluent application rates. Under miscanthus land use with no and high effluent application rates, net GHG equivalent on average was 4·3 Mg CO_2equ ha⁻¹ y⁻¹, which was larger when compared with that under the meadow land use (1·6 Mg CO_2equ ha⁻¹ y⁻¹). Miscanthus land use under medium rates of effluent application had similar net GHG equivalent (7·1 Mg CO_2equ ha⁻¹ y⁻¹) to the maize land use. The application of effluent did increase CO₂–C and N₂O–N emissions; but increases in above‐ground–below‐ground biomass production (1·6 Mg C ha⁻¹) in the meadow land use and C input from effluent retained in the soil in the miscanthus and maize land uses offset most of the effluent‐induced GHG equivalent emissions. Contribution of cumulative N₂O–N to GHG equivalent emissions in general was 11% when no effluent was applied and 22% when effluent was applied across land uses. Findings from this study show that land use changes from antecedent meadow to maize and miscanthus during the first year of establishment would result in net increase of GHG emissions. Published 2017. This article is a U.S. Government work and is in the public domain in the USA     

菜地土壤中氮肥的反硝化损失和N2O排放

A field experiment was conducted on Chinese cabbage （Brassica campestris L. ssp. pekinensis （Lour.） Olsson） in a Nanjing suburb in 2003. The experiment included 4 treatments in a randomized complete block design with 3 replicates： zero chemical fertilizer N （CK）; urea at rates of 300 kg N ha^-1 （U300） and 600 kg N ha^-1 （U600）, both as basal and two topdressings; and polymer-coated urea at a rate of 180 kg N ha^-1 （PCU180） as a basal application. The acetylene inhibition technique was used to measure denitrification （N2 ＋ N2O） from intact soil cores and N2O emissions in the absence of acetylene. Results showed that compared to （3K total denitrification losses were significantly greater （P ≤ 0.05） in the PCU180, U300, and U600 treatments,while N2O emissions in the U300 and U600 treatments were significantly higher （P ≤ 0.05） than （3K. In the U300 and U600 treatments peaks of denitrification and N2O emission were usually observed after N application. In the polymer-coated urea treatment （PCU180） during the period 20 to 40 days after transplanting, higher denitrification rates and N2O fluxes occurred. Compared with urea, polymer-coated urea did not show any effect on reducing denitrification losses and N2O emissions in terms of percentage of applied N. As temperature gradually decreased from transplanting to harvest, denitrification rates and N2O emissions tended to decrease. A significant （P ≤0.01） positive correlation occurred between denitrification （r = 0.872） or N2O emission （r = 0.781） flux densities and soil temperature in the CK treatment with a stable nitrate content during the whole growing season.     

Denitrification losses from 15N-labelled calcium nitrate fertilizer in a clay soil in the field

Calcium nitrate fertilizer containing 92.3 atoms % excess nitrogen-15 was applied on 5 May 1981 at a rate equivalent to 100 kg N ha^?1 to a clay soil in southern England cropped to winter wheat. Samples of the soil gases were collected frequently during the following 3 weeks. The soil oxygen concentration declined to 5% after 60 mm rain. A maximum of 1.5 ± 0.5 atom % N-15 enrichment in labelled N₂ gas (²⁹N₂) was detected in the soil atmosphere on 28 May. Total denitrification losses, calculated from air-filled pore space and rates of gas loss from the soil estimated using a Fick's law approximation, were 9.5 kg N ha^?1 with a daily rate of 0.30 ± 0.07 kg N ha^?1. Estimated total losses were greater than 30 kg N ha^?1, 93% in the form N₂, but the estimation depends on several assumptions about the amount of double labelled gas (³⁰N₂), rates of gas diffusion and flux.     

Net fluxes of CO2, but not N2O or CH4, are affected following agronomic-scale additions of urea to prairie and arable soils

While experimental addition of nitrogen (N) tends to enhance soil fluxes of carbon dioxide (CO₂), methane (CH₄), and nitrous oxide (N₂O), it is not known if lower and agronomic-scale additions of urea-N applied also enhance trace gas fluxes, particularly for semi-arid agricultural lands in the northern plains. We aimed to test if this were true at agronomic rates [low (11 kg N ha⁻¹), moderate (56 kg N ha⁻¹), and high (112 kg N ha⁻¹)] for central North Dakota arable and prairie soils using intact soil cores to minimize disturbance and simulate field conditions. Additions of urea to cores incubated at 21 °C and 57% water-filled pore space enhanced fluxes of CO₂ but not CH₄ and N₂O. At low, moderate, and high urea-N, CO₂ fluxes were significantly greater than control but not fluxes of CH₄ and N₂O. The increases in CO₂ emission with rate of urea-N application indicate that agronomic-scale N inputs may stimulate microbial carbon cycling in these soils, and that the contribution of CO₂ to net greenhouse gas source strength following fertilization of semi-arid agroecosystems may at times be greater than contributions by N₂O and CH₄.     

Soybean Residue Effect on Carbon Fractions and Gaseous Nitrogen Losses at Contrasting Moisture Contents

Most published studies related to crop effects on denitrification are not continuous and are based on the growing period. The objective of this work was to evaluate the effect of different amounts of soybean stubble, under different soil moisture contents, on gaseous nitrogen (N) losses by denitrification from an agricultural soil. The following soil moisture treatments were reached by adding distilled water to soil cores of a typic Hapludoll: 50 and 100% of water‐filled porosity space (WFPS). Residue treatments included no application of residues, amendment with 2600 kg ha^?1 of soybean residues, and amendment with 5200 kg ha^?1 of soybean residues. Cumulative nitrous oxide + dinitrogen (N₂O + N₂) emissions displayed great variability, ranging between 0 and 581.91 µg N kg^?1, which represented 0 to 3.93% of the N residue applied. Under 50% WFPS moisture conditions, statistical differences in cumulative N₂O + N₂ emissions between residue treatments were not detected (p = 0.21), whereas at saturation conditions, cumulative N₂O + N₂ emissions decreased with the application of increasing amounts of soybean residues (p = 0.017). Daily and cumulative N₂O + N₂ emissions significantly increased as soil moisture increased, except at soils amended with 5200 kg ha^?1 of soybean residues; this lack of statistical difference was probably due to the immobilization of native mineral N. Under 50% WFPS soil moisture contents, aeration seemed to be the main factor controlling redox conditions, limiting the denitrification process, and preventing differences in N emissions between residue treatments. The application of soybean residues to saturated soils notably decreased N₂O + N₂ emissions by denitrification through a strong mineral N immobilization into organic and nondenitrifiable forms.     

Denitrification losses from an Inceptisol field treated with mineral fertilizer or sewage sludge

In order to evaluate the climatic and soil variables which control the denitrification processes in the field, measurements of N₂O-losses using the C₂H₂ inhibition technique were carried out in an Inceptisol cropped with spring wheat. The silty sand was amended with mineral fertilizer (120 kg N ha^?1) or additionally with sewage sludge (620 kg total N ha^?1). Soil temperature, moisture, nitrate and available carbon, the release of nitrous oxide (N₂O) from the soil surface as well as the N₂O concentrations along the soil profile were measured from March until November 1985 The N₂O surface fluxes from the inorganically fertilized field were well correlated with those from the sewage sludge amended plots (r = 0.76). Multivariate correlation analyses show that particularly soil moisture and nitrate content had a significant effect on the nitrate respiration. The correlation with the soil water content was more clearly expressed by the N₂O surface fluxes than by the N₂O concentrations of the soil air. The N₂O surface fluxes during 1985 totalled about 3 kg N ha^?1 in the minerally fertilized field. Sewage sludge amendments increased the N₂O evolution by 5 times. Spatial variability was high and the N₂O surface fluxes were not well correlated (r = 0.4) with the N₂O concentrations in the soil atmosphere. These experiments provide the background data for a denitrification model and better knowledge about the variables which have to be considered for its validation.     

What predicts nitrous oxide emissions and denitrification N-loss from European soils?

N₂0 emissions and denitrification N-losses. precipitation, air temperature, soil moisture, bulk density and content of mineral N were monitored in 9 different agricultural soils in 6 European countries throughout the vegetation period (April to September) 1992 and 1993. N₂O emissions and denitrification N-losses were log-normal distributed, reflecting high temporal changes. While small flux rates (< 2 g N ha^?1 d^?1) were detectable every day, high rates (> 10 g N ha^?1 d^?1) were measured after fertilization. An attempt to relate the emission variables to climate and soil variables was made through the use of correlation analysis. The mean N₂0 emissions from soil were significantly correlated with the soil properties clay, organic C and mineral N content and the amount of applied mineral N fertilizer. The best prediction of the N₂O emission rates (r² = 0.734) was achieved by multiple linear regression using the soil parameter clay and mineral N. Only 50% of the observed variation could be explained by the factors C_org and mineral N, which describe the substrate availability for microbial processes. No successful statistical model was found for the prediction of denitrification N-losses.     

The influence of soluble carbon and fertilizer nitrogen on nitric oxide and nitrous oxide emissions from two contrasting agricultural soils

Contradictory effects of simultaneous available organic C and N sources on nitrous oxide (N₂O), carbon dioxide (CO₂) and nitric oxide (NO) fluxes are reported in the literature. In order to clarify this controversy, laboratory experiments were conduced on two different soils, a semiarid arable soil from Spain (soil I, pH=7.5, 0.8%C) and a grassland soil from Scotland (soil II, pH=5.5, 4.1%C). Soils were incubated at two different moisture contents, at a water filled pore space (WFPS) of 90% and 40%. Ammonium sulphate, added at rates equivalent to 200 and 50 kg N ha^?1, stimulated N₂O and NO emissions in both soils. Under wet conditions (90% WFPS), at high and low rates of N additions, cumulative N₂O emissions increased by 250.7 and 8.1 ng N₂O–N g^?1 in comparison to the control, respectively, in soil I and by 472.2 and 2.1 ng N₂O–N g^?1, respectively, in soil II. NO emissions only significantly increased in soil I at the high N application rate with and without glucose addition and at both 40% and 90% WFPS. In both soils additions of glucose together with the high N application rate (200 kg N ha^?1) reduced cumulative N₂O and NO emissions by 94% and 55% in soil I, and by 46% and 66% in soil II, respectively. These differences can be explained by differences in soil properties, including pH, soil mineral N and total and dissolved organic carbon content. It is speculated that nitrifier denitrification was the main source of NO and N₂O in the C-poor Spanish soil, and coupled nitrification–denitrification in the C-rich Scottish soil.     

The effect of nitrogen fertilization and no‐till duration on soil nitrogen supply power and post–spring thaw greenhouse‐gas emissions

With a world population now > 7 billion, it is imperative to conserve the arable land base, which is increasingly being leveraged by global demands for producing food, feed, fiber, fuel, and facilities (i.e., infra‐structure needs). The objective of this study was to determine the effect of varying fertilizer‐N rates on soil N availability, mineralization, and CO₂ and N₂O emissions of soils collected at adjacent locations with contrasting management histories: native prairie, short‐term (10 y), and long‐term (32 y) no‐till continuous‐cropping systems receiving five fertilizer‐N rates (0, 30, 60, 90, and 120 kg N ha^–1) for the previous 9 y on the same plots. Intact soil cores were collected from each site after snowmelt, maintained at field capacity, and incubated at 20°C for 6 weeks. Weekly assessments of soil nutrient availability along with CO₂ and N₂O emissions were completed. There was no difference in cumulative soil N supply between the unfertilized long‐term no‐till and native prairie soils, while annual fertilizer‐N additions of 120 kg N ha^–1 were required to restore the N‐supplying power of the short‐term no‐till soil to that of the undisturbed native prairie soil. The estimated cumulative CO₂‐C and N₂O‐N emissions among soils ranged from 231.8–474.7 g m^–2 to 183.9–862.5 mg m^–2, respectively. Highest CO₂ fluxes from the native prairie soil are consistent with its high organic matter content, elevated microbial activity, and contributions from root respiration. Repeated applications of ≥ 60 kg N ha^–1 resulted in greater residual inorganic‐N levels in the long‐term no‐till soil, which supported larger N₂O fluxes compared to the unfertilized control. The native prairie soil N₂O emissions were equal to those from both short‐ and long‐term no‐till soils receiving repeated fertilizer‐N applications at typical agronomic rates (e.g., 90 kg N ha^–1). Eighty‐eight percent of the native soil N₂O flux was emitted during the first 2 weeks and is probably characteristic of rapid denitrification rates during the dormant vegetative period after snowmelt within temperate native grasslands. There was a strong correlation (R² 0.64; p < 0.03) between measured soil Fe‐supply rate and N₂O flux, presumably due to anoxic microsites within soil aggregates resulting from increased microbial activity. The use of modern no‐till continuous diversified cropping systems, along with application of fertilizer N, enhances the soil N‐supplying power over the long‐term through the build‐up of mineralizable N and appears to be an effective management strategy for improving degraded soils, thus enhancing the productive capacity of agricultural ecosystems. However, accounting for N₂O emissions concomitant with repeated fertilizer‐N applications is imperative for properly assessing the net global warming potential of any land‐management system.     

Denitrification loss from a grassland soil in the field receiving different rates of nitrogen as ammonium nitrate

Denitrification loss from a loam under a cut ryegrass sward receiving 0, 250 and 500 kg N ha^?1 a^?1 in four equal amounts was measured during 14 months using the acetylene-inhibition technique. The rate of denitrification responded rapidly to changes in soil water content as affected by rain. Mean rates of denitrification exceeded 0.2 kg N ha^?1 day^?1 only when the soil water content was >20% (w/w) and nitrate was >5μ N g^?1 in the upper 20 cm of the profile and when soil temperature at 2 cm was >5–8°C. When the soil dried to a water content <20%, denitrification decreased to <0.05 kg N ha^?1 day^?1. Highest rates (up to 2.0 kg N ha^?1 day^?1) were observed following application of fertilizer to soil at a water content of about 30% (w/w) in early spring. Denitrification in the control plot during this period was generally about a hundredth of that in plots treated with ammonium nitrate. High rates of N₂O loss (up to 0.30 kg N ha^?1 day-1) were invariably associated with high rates of denitrification (> 0.2 kg N ha^?1 day^?1). However, within 2–3 weeks following application of fertilizer to the plot receiving 250 kg N ha^?1 a^?1 the soil acted as a sink for atmospheric N₂O when its water content was >20% and its temperature >5–8°C. Annual N losses arising from denitrification were 1.6, 11.1 and 29.1 kg N ha^?1 for the plots receiving 0, 250 and 500 kg N ha^?1 a^?1, respectively. More than 60% of the annual loss occurred during a period of 8 weeks when fertilizer was applied to soil with a water content >20%.     

N2O emissions from an irrigated and non‐irrigated organic soil in eastern Canada as influenced by N fertilizer addition

Drainage and cultivation of organic soils often result in large nitrous oxide (N₂O) emissions. The objective of this study was to assess the impacts of nitrogen (N) fertilizer on N₂O emissions from a cultivated organic soil located south of Montréal, QC, Canada, drained in 1930 and used since then for vegetable production. Fluxes of N₂O were measured weekly from May 2004 to November 2005 when snow cover was absent in irrigated and non‐irrigated plots receiving 0, 100 or 150 kg N ha⁻¹ as NH₄NO₃. Soil mineral N content, gas concentrations, temperature, water table height and water content were also measured to help explain variations in N₂O emissions. Annual emissions during the experiment were large, ranging from 3.6 to 40.2 kg N₂O‐N ha⁻¹ year⁻¹. The N₂O emissions were decreased by N fertilizer addition in the non‐irrigated site but not in the irrigated site. The absence of a positive influence of soil mineral N content on N₂O emissions was probably in part because up to 571 kg N ha⁻¹ were mineralized during the snow‐free season. Emissions of N₂O were positively correlated to soil CO₂ emissions and to variables associated with the extent of soil aeration such as soil oxygen concentration, precipitation and soil water table height, thereby indicating that soil moisture/aeration and carbon bioavailability were the main controls of N₂O emission. The large N₂O emissions observed in this study indicate that drained cultivated organic soils in eastern Canada have a potential for N₂O‐N losses similar to, or greater than, organic soils located in northern Europe.