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 Inorganic N Composition of Fertilizers on Nitrous Oxide Emission Associated with Nitrification and Denitrification

We studied the effect of repeated application (once every 2 d) of a fertilizer solution with different ratios of NH₄ ⁺ - and NO₃ ^?-N on N₂O emission from soil. After the excess fertilizer solution was drained from soil, the water content of soil was adjusted to 50% of the maximum water-holding capacity by suction at 6 × 10³ Pa. Repeated application of NH₄ ⁺- rich fertilizer solution stimulated nitrification in soil more than NO₃ ^?-rich fertilizer. Although the evolution of N₂O through nitrifier denitrification tended to increase with the repeated addition of a fertilizer solution rich in NH₄ ⁺ rather than in NO₃ ^?, the contribution of nitrifier denitrification remained at levels of 20 to 36% of the total emission regardless of the inorganic N composition. The total emission of N₂O also tended to increase with the application of NH₄ ⁺- rather than NO₃ ^?-rich fertilizer. It was suggested that the coupled process of nitrification and denitrification at micro-aerobic sites became important when fertilizer rich in NH₄ ⁺ was applied to soil under relatively aerobic conditions.     

Linkage of N2O emissions to the abundance of soil ammonia oxidizers and denitrifiers in purple soil under long-term fertilization

Abstract

Microbial nitrification and denitrification are responsible for the majority of soil nitrous (N₂O) emissions. In this study, N₂O emissions were measured and the abundance of ammonium oxidizers and denitrifiers were quantified in purple soil in a long-term fertilization experiment to explore their relationships. The average N₂O fluxes and abundance of the amoAgene in ammonia-oxidizing bacteria during the observed dry season were highest when treated with mixed nitrogen, phosphorus and potassium fertilizer (NPK) and a single N treatment (N) using NH₄HCO₃as the sole N source; lower values were obtained using organic manure with pig slurry and added NPK at a ratio of 40%:60% (OMNPK),organic manure with pig slurry (OM) and returning crop straw residue plus synthetic NH₄HCO₃fertilizer at a ratio of 15%:85% (SRNPK). The lowest N₂O fluxes were observed in the treatment that used crop straw residue(SR) and in the control with no fertilizer (CK). Soil NH₄⁺provides the substrate for nitrification generating N₂O as a byproduct. The N₂O flux was significantly correlated with the abundance of the amoA gene in ammonia-oxidizing bacteria (r = 0.984, p < 0.001), which was the main driver of nitrification. During the wet season, soil nitrate (NO₃^?) and soil organic matter (SOC) were found positively correlated with N₂O emissions (r = 0.774, p = 0.041 and r = 0.827, p = 0.015, respectively). The nirS gene showed a similar trend with N₂O fluxes. These results show the relationship between the abundance of soil microbes and N₂O emissions and suggest that N₂O emissions during the dry season were due to nitrification, whereas in wet season, denitrification might dominate N₂O emission.     

Time-lagged induction of N2O emission and its trade-off with NO emission from a nitrogen fertilized Andisol

Abstract

To understand the influence of basal application of N fertilizer on nitrification potential and N₂O and NO emissions, four soil samples were collected from an upland Andisol field just before (sample 1) and 4 (sample 2), 36 (sample 3) and 72 (sample 4) days after the basal application of N fertilizer during the Chinese cabbage growing season from 12 September to 30 November 2005. The potentials of N₂O production and nitrification of the soils were determined using a ¹⁵N tracer technique and the soils were incubated for 25 days at 25°C and 60% water-filled pore space (WFPS). The results revealed that as much as 84–97% N₂O and almost all NO were produced by nitrification. The ¹⁵N₂O emission peak occurred approximately 350 h after the beginning of incubation for samples 1 and 2, but just 48 h later in samples 3 and 4. Total ¹⁵N₂O emission during the 25-day incubation of samples 3 and 4 ranged from 190 to 198 µg N kg^?1 soil, which was significantly higher than the 99–108 µg N kg^?1 soil recorded in samples 1 and 2. Basal application of N fertilizer did not immediately increase the nitrification potential and the ratio of N₂O to N added, but did dramatically increase the nitrification potential and the ratio of N₂O to N added as (¹⁵NH₄)₂SO₄ 36–72 days after the basal N fertilizer was added. In contrast, NO emission was negatively correlated with nitrification potential and total N₂O emission. As a result, a trade-off relationship between total NO and N₂O emissions was identified. The results indicated that there was a time-lagged induction of the change of N turnover in the soil, which was possibly caused by slow population growth of the nitrifiers and/or a slow shift in the microbial community in the soil.     

Grassland renovation increases N2O emission from a volcanic grassland soil in Nasu,Japan

Abstract

To investigate the effects of renovation (ploughing and resowing) on nitrous oxide (N₂O) emissions from grassland soil, we measured N₂O fluxes from renovated and unrenovated (control) grassland plots. On 22 August in both 2005 and 2006 we harvested the sward, ploughed the surface soil and then mixed roots and stubble into the surface soil with a rotovator. Next, we compacted the soil surface with a land roller, spread fertilizer at 40 kg N ha^?1 on the soil surface and sowed orchardgrass (Dactylis glomerata L., Natsumidori). In the control plot, we just harvested the sward and spread fertilizer. We determined N₂O fluxes for 2 months after the renovation using a vented closed chamber. During the first 2 weeks, the renovated plot produced much more N₂O than the control plot, suggesting that N was quickly mineralized from the incorporated roots and stubble. Even after 2 weeks, however, large N₂O emissions from the renovated plot were recorded after rainfall, when the soil surface was warmed by sunshine and the soil temperature rose 2.7–3.0°C more than that of the control plot. In 2005, during the 67-day period from 19 August to 26 October, the renovated and control plots emitted 5.3 ± 1.4 and 2.8 ± 0.7 kg N₂O-N ha^?1, with maximum fluxes of 3,659 and 1,322 µg N₂O-N m^?2 h^?1, respectively. In 2006, during the 65-day period from 21 August to 26 October, the renovated and control plots emitted 2.1 ± 0.6 and 0.96 ± 0.42 kg N₂O-N ha^?1, with maximum fluxes of 706 and 175 µg N₂O-N m^?2 h^?1, respectively. The cumulative N₂O emissions from plots in 2005 were greater than those in 2006, presumably because rainfall just after renovation was greater in 2005 than in 2006. These results suggest that incorporated roots and stubble may enlarge the anaerobic microsites in the soil in its decomposing process and increase the N₂O production derived from the residues and the fertilizer. In addition, rainfall and soil moisture and temperature conditions during and after renovation may control the cumulative N₂O emission.     

Nitrogen transformation rates and N<Subscript>2</Subscript>O producing pathways in two pasture soils

Purpose

Better understanding of N transformations and the regulation of N₂O-related N transformation processes in pasture soil contributes significantly to N fertilizer management and development of targeted mitigation strategies.

Materials and methods

¹⁵N tracer technique combined with acetylene (C₂H₂) method was used to measure gross N transformation rates and to distinguish pathways of N₂O production in two Australian pasture soils. The soils were collected from Glenormiston (GN) and Terang (TR), Victoria, Australia, and incubated at a soil moisture content of 60% water-filled pore space (WFPS) and at temperature of 20 °C.

Results and discussion

Two tested pasture soils were characterized by high mineralization and immobilization turnover. The average gross N nitrification rate (n_tot) was 7.28 mg N kg^?1 day^?1 in TR soil () and 5.79 mg N kg^?1 day^?1 in GN soil. Heterotrophic nitrification rates (n_h), which accounting for 50.8 and 41.9% of n_tot, and 23.4 and 30.1% of N₂O emissions in GN and TR soils, respectively, played a role similar with autotrophic nitrification in total nitrification and N₂O emission. Denitrification rates in two pasture soils were as low as 0.003–0.004 mg N kg^?1 day^?1 under selected conditions but contributed more than 30% of N₂O emissions.

Conclusions

Results demonstrated that two tested pasture soils were characterized by fast N transformation rates of mineralization, immobilization, and nitrification. Heterotrophic nitrification could be an important NO₃^?–N production transformation process in studied pasture soils. Except for autotrophic nitrification, roles of heterotrophic nitrification and denitrification in N₂O emission in two pasture soils should be considered when developing mitigation strategies.

     

Methane uptake and nitrous oxide emission in Japanese forest soils and their relationship to soil and vegetation types

Abstract

To determine the means and variations in CH₄ uptake and N₂O emission in the dominant soil and vegetation types to enable estimation of annual gases fluxes in the forest land of Japan, we measured monthly fluxes of both gases using a closed-chamber technique at 26 sites throughout Japan over 2 years. No clear seasonal changes in CH₄ uptake rates were observed at most sites. N₂O emission was mostly low throughout the year, but was higher in summer at most sites. The annual mean rates of CH₄ uptake and N₂O emission (all sites combined) were 66 (2.9–175) µg CH₄-C m^?2 h^?1 and 1.88 (0.17–12.5) µg N₂O-N m^?2 h^?1, respectively. Annual changes in these fluxes over the 2 years were small. Significant differences in CH₄ uptake were found among soil types (P < 0.05). The mean CH₄ uptake rates (µg CH₄-C m^?2 h^?1) were as follows: Black soil (95 ± 39, mean ± standard deviation [SD]) > Brown forest soil (60 ± 27) ≥ other soils (20 ± 24). N₂O emission rates differed significantly among vegetation types (P < 0.05). The mean N₂O emission rates (µg N₂O-N m^?2 h^?1) were as follows: Japanese cedar (4.0 ± 2.3) ≥ Japanese cypress (2.6 ± 3.4) > hardwoods (0.8 ± 2.2) = other conifers (0.7 ± 1.4). The CH₄ uptake rates in Japanese temperate forests were relatively higher than those in Europe and the USA (11–43 µg CH₄-C m^?2 h^?1), and the N₂O emission rates in Japan were lower than those reported for temperate forests (0.23–252 µg N₂O-N m^?2 h^?1). Using land area data of vegetation cover and soil distribution, the amount of annual CH₄ uptake and N₂O emission in the Japanese forest land was estimated to be 124 Gg CH₄-C year^?1 with 39% uncertainty and 3.3 Gg N₂O-N year^?1 with 76% uncertainty, respectively.     

Interactive effects of ammonium application rates and temperature on nitrous oxide emission from tropical agricultural soil

Emissions of nitrous oxide (N₂O), a potent greenhouse gas, from agricultural soil have been recognized to be affected by nitrogen (N) application and temperature. Most of the previous studies were carried out to determine effects of temperature on N₂O emissions at a fixed N application rate or those of N application rates at a specific temperature. Knowledge about the effects of different ammonium (NH₄⁺) application rates and temperatures on N₂O emissions from tropical agricultural soil and their interactions is limited. Five grams of air-dried sandy loam soil, collected in Central Vietnam, were adjusted to 0, 400, 800 and 1200 mg NH₄-N kg^–1 soil (abbreviated as 0 N, 400 N, 800 N and 1200 N, respectively) at 60% water holding capacity were aerobically incubated at 20°C, 25°C, 30°C or 35°C for 28 days. Mineral N contents and N₂O emission rates were determined on days 1, 3, 5, 7, 14, 21 and 28. Cumulative N₂O emissions for 28 days increased with increasing NH₄⁺ application rates from 0 to 800 mg N kg^–1 and then declined to 1200 mg N kg^–1. Cumulative N₂O emissions increased in the order of 35°C, 20°C, 30°C and 25°C. This lowest emission at 35°C occurred because N₂O production was derived only from autotrophic nitrification while other N₂O production processes, e.g., nitrifier denitrification and coupled nitrification-denitrification occurred at lower temperatures. More specifically, cumulative N₂O emissions peaked at 800 N and 25°C, and the lowest emissions occurred at 1200 N and 35°C. In conclusion, N₂O emissions were not exponentially correlated with NH₄⁺ application rates or temperatures. Higher NH₄⁺ application rates at higher temperatures suppressed N₂O emissions.     

Effects of soil moisture on gross N transformations and N2O emission in acid subtropical forest soils

Soil moisture changes, arising from seasonal variation or from global climate changes, could influence soil nitrogen (N) transformation rates and N availability in unfertilized subtropical forests. A ¹⁵?N dilution study was carried out to investigate the effects of soil moisture change (30–90 % water-holding capacity (WHC)) on potential gross N transformation rates and N₂O and NO emissions in two contrasting (broad-leaved vs. coniferous) subtropical forest soils. Gross N mineralization rates were more sensitive to soil moisture change than gross NH₄ ⁺ immobilization rates for both forest soils. Gross nitrification rates gradually increased with increasing soil moisture in both forest soils. Thus, enhanced N availability at higher soil moisture values was attributed to increasing gross N mineralization and nitrification rates over the immobilization rate. The natural N enrichment in humid subtropical forest soils may partially be due to fast N mineralization and nitrification under relatively higher soil moisture. In broad-leaved forest soil, the high N₂O and NO emissions occurred at 30 % WHC, while the reverse was true in coniferous forest soil. Therefore, we propose that there are different mechanisms regulating N₂O and NO emissions between broad-leaved and coniferous forest soils. In coniferous forest soil, nitrification may be the primary process responsible for N₂O and NO emissions, while in broad-leaved forest soil, N₂O and NO emissions may originate from the denitrification process.     

Lime-nitrogen application reduces N2O emission from a vegetable field with imperfectly-drained sandy clay-loam soil

Abstract

We studied the effect of lime-nitrogen (calcium cyanamide, CaCN₂) application on the emission of nitrous oxide (N₂O) from a vegetable field with imperfectly-drained sandy clay-loam soil. Lime-nitrogen acts as both a pesticide and a fertilizer. During the decomposition of lime-nitrogen in the soil, dicyandiamide (DCD), a nitrification inhibitor, is formed, and as a result lime-nitrogen application may mitigate N₂O emission from the soil. The study design consisted of three different nitrogen-application treatments in field plots with a randomized block design. The nitrogen application treatments were: CF (chemical fertilizer), LN (all nitrogen fertilizer applied as lime-nitrogen), and CFD (chemical fertilizer containing DCD). Soil nitrification activity was lower in the LN and CFD plots than in the CF plots, and nitrification was inhibited for a longer period in the LN plots than in the CFD plots. In the LN plots, N₂O emission was lower than those of other treatments from 20 to 40 days after fertilization, a period when large peaks of N₂O emission were observed after rainfall in the CF and CFD plots. Cumulative N₂O emission over 63 days in the CF plots (mean ± standard deviation: 30.2 ± 14.4 mg N₂O m^?2) and CFD plots (24.3 ± 10.8 mg N₂O m^?2) was significantly higher than that in the LN plots (10.7 ± 1.2 mg N₂O m^?2; P < 0.05). Our results suggested that lime-nitrogen application decreased N₂O emission by inhibiting both nitrification and denitrification.     

Effects of carbon and phosphorus addition on microbial respiration,N<Subscript>2</Subscript>O emission,and gross nitrogen mineralization in a phosphorus-limited grassland soil

Soil microbes are frequently limited by carbon (C), but also have a high phosphorus (P) requirement. Little is known about the effect of P availability relative to the availability of C on soil microbial activity. In two separate experiments, we assessed the effect of P addition (20 mg P kg^?1 soil) with and without glucose addition (500 mg C kg^?1 soil) on gross nitrogen (N) mineralization (¹⁵N pool dilution method), microbial respiration, and nitrous oxide (N₂O) emission in a grassland soil. In the first experiment, soils were incubated for 13 days at 90% water holding capacity (WHC) with addition of NO₃^? (99 mg N kg^?1 soil) to support denitrification. Addition of C and P had no effect on gross N mineralization. Initially, N₂O emission significantly increased with glucose, but it decreased at later stages of the incubation, suggesting a shift from C to NO₃^? limitation of denitrifiers. P addition increased the N₂O/CO₂ ratio without glucose but decreased it with glucose addition. Furthermore, the ¹⁵N recovery was lowest with glucose and without P addition, suggesting a glucose by P interaction on the denitrifying community. In the second experiment, soils were incubated for 2 days at 75% WHC without N addition. Glucose addition increased soil ¹⁵N recovery, but had no effect on gross N mineralization. Possibly, glucose addition increased short-term microbial N immobilization, thereby reducing N-substrates for nitrification and denitrification under more aerobic conditions. Our results indicate that both C and P affect N transformations in this grassland soil.     

Nitrogen Removal, N2O Emission, and NH3 Volatilization Under Different Water Levels in a Vertical Flow Treatment System

Two series of laboratory-scale vertical flow systems (flooded and nonflooded columns) were designed to compare nitrogen removal performance, nitrous oxide emission, and ammonia volatilization under different water levels upon treating diluted digested livestock liquid. In these systems, influent was supplied at three hydraulic loading rates (HLRs of 1.25, 2.5, and 5 cm day^?1) during stage 1 and the rates were doubled during stage 2 when the water levels of nonflooded columns were elevated from zero to half the height of the soil column. After hydraulic loading rates doubled, the average removal rates of total nitrogen in flooded columns varied from 1.27 to 2.94 g^?2 day^?1 and those in nonflooded columns ranged from 1.23 to 3.88 g^?2 day^?1. The T-N removal at an HLR of 10 cm day^?1 in the nonflooded column with an elevated water table level had higher efficiency than that in the flooded column, suggesting T-N removal is enhanced in the nonflooded column probably due to the improved coupled nitrification–denitrification process under the elevated water table level condition. On the other hand, there was a significant correlation (r ² = 0.532, p < 0.001) between the N₂O flux and redox potential that mainly corresponded to water levels and HLRs, suggesting anoxic or aerobic conditions stimulate N₂O emission by enhancing the nitrification (nitrification–denitrification) process. In contrast, NH₃ volatilization had a high flux in the anaerobic condition mainly because of flooding. Based on the experimental results, it is hypothesized a nonflooded condition with higher water table level (Eh range of ?160 to +260 mV) would be suitable to reduce N₂O emission and NH₃ volatilization peak value by at least half while maintaining relatively efficient nitrogen removal performance.     

土壤温度、水分和NH4+-N浓度对土壤硝化反应速度及N2O排放的影响

硝化反应是土壤、特别是干旱半干旱地区农业土壤N2O产生的重要途径之一。但是,目前环境条件对硝化反应中N2O排放的影响研究较少,而在国内外通用的几个模型中均用固定比例估算硝化反应过程中N2O的排放。本文通过砂壤土培养试验,研究了土壤温度、水分和NH4+-N浓度对硝化反应速度及硝化反应中N2O排放的影响,并用数学模型定量表示了各因素对硝化反应的作用,用最小二乘法最优拟合求得该土壤的最大硝化反应速度及N2O最大排放比例。结果表明,随着温度升高,硝化反应速度呈指数增长;水分含量由20%充水孔隙度(WFPS)增加到40%WFPS时,反应速度增加,水分含量增加到60%WFPS时反应速度略有降低;NH4+-N浓度增加对硝化反应速度起抑制作用。用米氏方程描述该土壤的硝化反应过程,其最大硝化反应速度为6.67mg·kg?1·d?1。硝化反应中N2O排放比例随温度升高而降低;随NH4+-N浓度增加而略有增加;20%和40%WFPS水分含量时,硝化反应中N2O排放比例为0.43%～1.50%,最小二乘法求得的最大比例为3.03%,60%WFPS时可能由于反硝化作用,N2O排放比例急剧增加,还需进一步研究水分对硝化反应中N2O排放的影响。     

Effects of application of lime nitrogen and dicyandiamide on nitrous oxide emissions from green tea fields

Abstract

The aim of this study was to assess the mitigating effects of lime nitrogen (calcium cyanamide) and dicyandiamide (DCD) application on nitrous oxide (N₂O) emissions from fields of green tea [Camellia sinensis (L.) Kuntze]. The study was conducted in experimental tea fields in which the fertilizer application rate was 544 kg nitrogen (N) ha^?1 yr^?1 for 2 years. The mean cumulative N₂O flux from the soil between the canopies of tea plants for 2 years was 7.1 ± 0.9 kg N ha^?1 yr^?1 in control plots. The cumulative N₂O flux in the plots supplemented with lime nitrogen was 3.5 ± 0.1 kgN ha^?1, approximately 51% lower than that in control plots. This reduction was due to the inhibition of nitrification by DCD, which was produced from the lime nitrogen. In addition, the increase in soil pH by lime in the lime nitrogen may also be another reason for the decreased N₂O emissions from soil in LN plots. Meanwhile, the cumulative N₂O flux in DCD plots was not significantly different from that in control plots. The seasonal variability in N₂O emissions in DCD plots differed from that in control plots and application of DCD sometimes increased N₂O emissions from tea field soil. The nitrification inhibition effect of lime nitrogen and DCD helped to delay nitrification of ammonium-nitrogen (NH₄⁺-N), leading to high NH₄⁺-N concentrations and a high ratio of NH₄⁺-N /nitrate-nitrogen (NO₃^–-N) in the soil. The inhibitors delayed the formation of NO₃^–-N in soil. N uptake by tea plants was almost the same among all three treatments.     

Lime-nitrogen application affects nitrification, denitrification, and N2O emission in an acidic tea soil

Lime-N (calcium cyanamide, CaCN₂) acts as both fertilizer and pesticide. Lime-N may reduce nitrous oxide (N₂O) emission from soil, although its effectiveness and the relative mechanisms are not well understood. The aim of the study was to quantify the effect of lime-N on N₂O emission from the acidic soil of tea fields. The study design consisted of two treatments: conventional fertilizer (CF) (application of conventional organo-chemical fertilizer) and lime-N (LN) (application of approximately 53 % of the applied N as lime-N and the remaining as conventional organo-chemical fertilizer). Both treatments had the same amount of N, P₂O₅, and K₂O applied to soil between plant canopies; fertilizer was incorporated into soil. We measured N₂O emissions and environmental and microbial parameters of soil between plant canopies and under the canopy of tea plants, including the concentrations of dicyandiamide and cyanamide derived from lime-N. Nitrous oxide emission from soil between plant canopies was lower in the LN treatment than in the CF treatment, and soil ammonium oxidation activity and soil denitrification rate decreased after lime-N application. We applied the acetylene inhibition technique and analyzed isotopomer ratios of N₂O; the results of both techniques suggested that denitrification was the major process of N₂O production in the soil between plant canopies, despite relatively low water-filled pore space. Cumulative N₂O emission over the 366 days of the experiment was 36.0 % lower in the LN treatment than in the CF treatment (P?<?0.05). Our results suggest that lime-N application decreases N₂O emission by inhibiting both nitrification and denitrification processes in the acidic soil.     

Nitrous oxide production by denitrification and nitrification in temperate forest, grassland and agricultural soils

Nitrous oxide is produced in soils by biological denitrification and nitrification. To improve the fundamental understanding of the processes leading to N₂O fluxes from soils, the production of N₂O from denitrification and nitrification in spruce forest, beech forest, riparian grassland, coastal grassland and an agricultural field were studied. Samples were taken at a high and a low position along a topographic gradient in each site in the spring and autumn when the largest N₂O fluxes were expected. They were incubated after being amended with N, and C₂H₂ was used as biological inhibitor to distinguish nitrification and denitrification. The N₂O production in the low landscape position varied between 32 and 121 ng N cm^?3 h^?1 in the riparian grassland. 9 and 26 ng N cm^?3 h^?1 in the coastal grassland, and 135 and 195 ng N cm^?3 h^?1 in the agricultural field which was 10–100 times more than in the high positions where rates ranged between 3 and 5 ng N cm^?3 h^?1, 0.3 and 0.4 ng N cm^?3 h^?1, and 7 and 10 ng N cm^?3 h^?1, respectively. These differences almost certainly arose because the soil in the low positions was wetter and contained more organic matter. In the two forests N₂O production was less than 1 ng N cm^?3 h^?1, strongly inhibited by O₂, and not influenced by landscape position. Nitrification contributed to more than 60% of total N₂O production in the riparian grassland. In the agricultural field nitrification produced 13–74% of the total N₂O in the low position, and 10–88% in the high position. Denitrification was the dominant source of N₂O in the coastal grassland except at the low position in the autumn where nitrification produced 60% of the total N₂O. In the two forests where the soil had small nitrification potentials denitrification was the only source of N₂O. In the other sites nitrification and denitrification potentials were large and of identical magnitude. The results emphasize the need to separate nitrification and denitrification at the process level and to recognize topography at the field scale when modelling N₂O effluxes from soil.     

Abiotic nitrous oxide production from hydroxylamine in soils and their dependence on soil properties

Despite the fact that microbial nitrification and denitrification are considered the major soil N₂O emission sources, especially from agricultural soils, several abiotic reactions involving the nitrification intermediate hydroxylamine (NH₂OH) have been identified leading to N₂O emissions, but are being neglected in most current studies. Here, we studied N₂O formation from NH₂OH in cropland, grassland, and forest soils in laboratory incubation experiments. Incubations were conducted with and without the addition of NH₂OH to non-sterile and sterile soil samples. N₂O evolution was quantified with gas chromatography and further analyzed with online laser absorption spectroscopy. Additionally, the isotopic signature of the produced N₂O (δ¹⁵N, δ¹⁸O, and ¹⁵N site preference) was analyzed with isotope ratio mass spectrometry. While the forest soil samples showed hardly any N₂O evolution upon the addition of NH₂OH, immediate and very large formation of N₂O was observed in the cropland soil, also in sterilized samples. Correlation analysis revealed soil parameters that might explain the variability of NH₂OH-induced N₂O production to be: soil pH, C/N ratio, and Mn content. Our results suggest a coupled biotic–abiotic production of N₂O during nitrification, e.g. due to leakage of the nitrification intermediate NH₂OH with subsequent reaction with the soil matrix.     

Evaluation of nitrate and ammonium as sources of NO and N2O emissions from black earth soils (Haplic Chernozem) based on 15N field experiments

Nitrous oxide (N₂O) and nitric oxide (NO) released from soil is a concern since it can act as a potential atmospheric pollutant and it represents a loss of N from the soil. These gases are present in the atmosphere in trace amounts and are important to atmospheric chemistry and earth's radiative balance. Nitric oxide (NO) does not directly contribute to the greenhouse effect, but it contributes to climate forcing through its role in photochemistry of hydroxyl radicals and ozone and plays a key role in air quality issues. Nitrification and denitrification have been identified as major controlling microbial processes in soils responsible for the formation of NO and N₂O. To elucidate the contribution of both processes to the release of NO and N₂O from loess-black earth soils under field conditions—i.e. to evaluate nitrate and ammonium as sources of NO and N₂O emission—two field experiments with either [¹⁵N] nitrate (NO₃^?) or [¹⁵N] ammonium (NH₄⁺) labelling have been conducted at two sites differing in soil organic matter content (high and normal SOM). [¹⁵N] nitrate treatments revealed that denitrification of NO₃^? represents the main pathway of soil N₂O release. On average 76% and 54% of N₂O was emitted during denitrification from soils with high and normal SOM content, respectively. Contrarily, denitrification contributed on average only 17% and 12% of released NO from soil with high and normal SOM content, respectively. The [¹⁵N]ammonium treatments revealed that nitrification of NH₄⁺ is the major process responsible for soil NO emission. SOM content of the loess-black earth soil significantly influenced NO and N₂O emission. The soil with the higher SOM content showed lower NO emission but drastically increased N₂O emission after nitrate fertilisation. In particular the soil with high SOM content exhibited a high sorption capacity for ammonium ions which led to unexpected results after fertilisation with [¹⁵N]ammonium. To explain this results a revised concept containing three different interacting soil ammonium pools have been hypothesised.     

Microbial pathways for nitrous oxide emissions from sheep urine and dung in a typical steppe grassland

The aim of this study was to determine the responses of nitrifiers and denitrifiers to understand microbial pathways of nitrous oxide (N₂O) emissions in grassland soils that received inputs of sheep excreta. Sheep dung and synthetic sheep urine were applied at three different rates, simulating a single, double, or triple overlapping of urine or dung depositions in the field. Quantitative PCR and high-throughput sequencing were combined with process-based modeling to understand effects of sheep excreta on microbial populations and on pathways for N₂O production. Results showed that emissions of N₂O from urine were significantly higher than from dung, ranging from 0.12 to 0.78 kg N₂O-N ha^?1 during the 3 months. The N₂O emissions were significantly related to the bacterial amoA (r?=?0.373, P?<?0.001) and nirK (r?=?0.614, P?<?0.001) gene abundances. It was autotrophic nitrification that dominated N₂O production in the low urine-N rate soils, whereas it was denitrification (including nitrifier denitrification and heterotrophic denitrification) that dominated N₂O production in the high urine-N rate soils. Nitrifier denitrification was responsible for most of the N₂O emissions in the dung-treated soils. This study suggests that nitrifier denitrification is indeed an important pathway for N₂O emissions in these low fertility and dry grazed grassland ecosystems.     

GREENHOUSE GAS EMISSIONS FROM AN ALKALINE SALINE SOIL CULTIVATED WITH MAIZE (ZEA MAYS L.) AND AMENDED WITH ANAEROBICALLY DIGESTED COW MANURE: A GREENHOUSE EXPERIMENT

Sludge derived from cow manure anaerobically digested to produce biogas (methane; CH₄) was applied to maize (Zea mays L.) cultivated in a nutrient-low, alkaline, saline soil with electrolytic conductivity 9.4 dS m^?1 and pH 9.3. Carbon dioxide (CO₂) emission increased 3.1 times when sludge was applied to soil, 1.6 times when cultivated with maize and 3.5 times in sludge-amended maize cultivated soil compared to the unamended uncultivated soil (1.51 mg C kg^?1 soil day^?1). Nitrous oxide (N₂O) emission from unamended soil was -0.0004 μg nitrogen (N) kg^?1 soil day^?1 and similar from soil cultivated with maize (0.27 μg N kg^?1 soil day^?1). Application of sludge increased the N₂O emission to 4.59 μg N kg^?1 soil day^?1, but cultivating this soil reduced it to 2.42 μg N kg^?1 soil day^?1. It was found that application of anaerobic digested cow manure stimulated maize development in an alkaline saline soil and increased emissions of CO₂ and N₂O.