Site of nitrous oxide production in field soils

Summary Nitrous oxide (N₂O) fluxes at the soil surface and concentrations at 0.1, 0.2, and 0.3 m were determined in a 40-year-old planted tallgrass (XXX) prairie, a 40-year-old white pine (Pinus strobus) plantation, and field plots treated annually for 18 years either with 33 metric tons of manure ha^–1 (330 kg N ha^–1) and NH₄NO₃ (80 kg N ha^–1) or with only NH₄NO₃ (control). Nitrous oxide fluxes from the prairie, forest, manure-amended, and control sites from 13 May to 10 November 1980 ranged from 0.2 to 1.3, 3.5 to 19.5, 3.7 to 79.0, and 1.7 to 24.8 ng N₂O-N m^–2s^–1, respectively. We observed periods when there was no apparent relationship between the N₂O flux from the surface and N₂O concentrations in the soil profile. This was generally the case in the prairie and in the field sites following the application of N fertilizer. The N₂O concentrations in the soil profile increased markedly and coincided with increased soil water content following periods of heavy rainfall for all sites except the prairie. Nitrous oxide concentration gradients indicate that following heavy rainfalls the site of N₂O production was moved from the surface deeper into the soil profile. We suggest that the source of N₂O production near the surface is nitrification and that N₂O is produced by denitrification of NO₃ leached into the soil following heavy rainfall.     

土壤N2O和NO产生机制研究进展

N2O和NO是大气中两种重要的活性氮气体,强烈影响着全球变化和生态环境。土壤是N2O和NO的重要排放源,生物和非生物途径均可产生N2O和NO。本文详细论述了自养硝化、异养硝化、生物反硝化、化学反硝化、硝化细菌反硝化和硝态氮异化还原成铵作用产生N2O和（或）NO的机制,并对研究中存在的一些问题进行了探讨。     

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.     

Effects of various nitrogen fertilizers on emission of nitrous oxide from soils

Summary Field studies of the effects of different N fertilizers on emission of nitrous oxide (N20) from three Iowa soils showed that the N₂O emissions induced by application of 180 kg ha^–1 fertilizer N as anhydrous ammonia greatly exceeded those induced by application of the same amount of fertilizer N as aqueous ammonia or urea. On average, the emission of N₂O-N induced by anhydrous ammonia was more than 13 times that induced by aqueous ammonia or urea and represented 1.2% of the anhydrous ammonia N applied. Experiments with one soil showed that the N₂O emission induced by anhydrous ammonia was more than 17 times that induced by the same amount of N as calcium nitrate. These findings confirm indications from previous work that anhydrous ammonia has a much greater effect on emission of N₂O from soils than do other commonly used N fertilizers and merits special attention in research relating to the potential adverse climatic effect of N fertilization of soils.Laboratory studies of the effect of different amounts of NH₄OH on emission of N₂O from Webster soil showed that the emission of N₂O-N induced by addition of 100 g NH₄OH-N g^–1 soil represented only 0.18% of the N applied, whereas the emissions induced by additions of 500 and 1 000 g NH4OH-N g^–1 soil represented 1.15% and 1.19%, respectively, of the N applied. This suggests that the exceptionally large emissions of N₂O induced by anhydrous ammonia fertilization are due, at least in part, to the fact that the customary method of applying this fertilizer by injection into soil produces highly alkaline soil zones of high ammonium-N concentration that do not occur when urea or aqueous ammonia fertilizers are broadcast and incorporated into soil.     

Relationships between soil moisture content and nitrous oxide production during nitrification and denitrification

Summary The effect of soil water content [60%–100% water-holding capacity (WHC)] on N₂O production during autotrophic nitrification and denitrification in a loam soil was studied in a laboratory experiment by selectively inhibiting nitrification with a low C₂H₂ concentration (2.1 Pa). Nitrifiers usually produced more N₂O than denitrifiers. During an initial experimental period of 0–6 days the nitrifiers produced more N₂O than the denitrifiers by a factor ranging from 1.4 to 16.5, depending on the water content and length of incubation. The highest N₂O production rate by nitrifiers was observed at 90% WHC, when the soil had become partly anaerobic, as indicated by the high denitrification rate. At 100% WHC there were large gaseous losses from denitrification, while nitrification losses were smaller except for the first period of measurement, when there was still some O₂ remaining in the soil. The use of 10 kPa C₂H₂ to inhibit reduction of N₂O to N₂ stimulated the denitrification process during prolonged incubation over several days; thus the method is unsuitable for long-term studies.     

Formation of nitrous oxide and dinitrogen by chemical decomposition of hydroxylamine in soils

Soil properties affecting formation of nitrous oxide (N₂O) and dinitrogen (N₂) by chemical decomposition of hydroxylamine (NH₂OH) in soils were studied using 19 soils selected to obtain a wide range in properties. It was found that production of N₂O by chemical decomposition of NH₂OH in soils is more rapid than production of N₂ and that, except with calcareous soils, N₂O production greatly exceeds N₂ production. Studies of the correlations between various soil properties and formation of N₂O and N₂ by decomposition of NH₂OH showed that production of N₂O was very highly correlated with exchangeable and oxidized Mn in the soils studied, and that production of N₂ was very highly correlated with pH, CaCO₃ equivalent, exchangeable Ca²⁺, and oxidized Mn. Production of N₂ in neutral and acidic soils was highly correlated with both exchangeable and oxidized Mn, and production of N₂ in calcareous soils was significantly correlated with oxidized Fe. The deductions from these correlations that Mn compounds are involved in the reactions leading to formation of N₂O and N₂ by chemical decomposition of NH₂OH in soils, and that CaCO₃ and Fe compounds are involved in the reactions leading to formation of N₂ in calcareous soils, were supported by studies of N₂O and N₂ production through reactions of Mn and Fe compounds with NH₂OH in the presence and absence of CaCO₃. Production of N₂O via chemical decomposition of NH₂OH in soils greatly exceeds production of N₂O through chemical decomposition of nitrite (i.e. via chemodenitrification), and the amount of N₂ produced by decomposition of NH₂OH in most soils exceeds the amount produced by decomposition of nitrite. Work reported indicates that, if N₂O is formed in soils through nonbiological transformations of NH₂OH produced by soil microorganisms, very little of this gas is generated by the reaction of NH₂OH with nitrite frequently postulated as a mechanism of N₂O production in soils (NH₂OH + HNO₂ → N₂O + 2H₂O).     

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

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

Small-scale heterogeneity in carbon dioxide, nitrous oxide and methane production from aggregates of a cultivated sandy-loam soil

Spatial variability in carbon dioxide (CO₂), nitrous oxide (N₂O) and methane (CH₄) emissions from soil is related to the distribution of microsites where these gases are produced. Porous soil aggregates may possess aerobic and anaerobic microsites, depending on the water content of pores. The purpose of this study was to determine how production of CO₂, N₂O and CH₄ was affected by aggregate size and soil water content. An air-dry sandy loam soil was sieved to generate three aggregate fractions (<0.25 mm, 0.25–2 mm and 2–6 mm) and bulk soil (<2 mm). Aggregate fractions and bulk soil were moistened (60% water-filled pore space, WFPS) and pre-incubated to restore microbial activity, then gradually dried or moistened to 20%, 40%, 60% or 80% WFPS and incubated at 25 °C for 48 h. Soil respiration peaked at 40% WFPS, presumably because this was the optimum level for heterotrophic microorganisms, and at 80% WFPS, which corresponded to the peak N₂O production. More CO₂ was produced by microaggregates (<0.25 mm) than macroaggregate (>0.25 mm) fractions. Incubation of aggregate fractions and soil at 80% WFPS with acetylene (10 Pa and 10 kPa) and without acetylene showed that denitrification was responsible for 95% of N₂O production from microaggregates, while nitrification accounted for 97–99% of the N₂O produced by macroaggregates and bulk soil. This suggests that oxygen (O₂) diffusion into and around microaggregates was constrained, whereas macroaggregates remained aerobic at 80% WFPS. Methane consumption and production were measured in aggregates, reaching 1.1–6.4 ng CH₄–C kg⁻¹ soil h⁻¹ as aggregate fractions and soil became wetter. For the sandy-loam soil studied, we conclude that nitrification in aerobic microsites contributed importantly to total N₂O production, even when the soil water content permitted denitrification and CH₄ production in anaerobic microsites. The relevance of these findings to microbial processes controlling N₂O production at the field scale remains to be confirmed.     

Influence of nitrification inhibitors on nitrification and nitrous oxide (N2O) emission from a clay loam soil fertilized with urea

Laboratory incubation experiments were conducted to compare the effects of the nitrification inhibitors 3,4-dimethylpyrazole phosphate (DMPP) and 2-Chloro-6-(trichloromethyl)-pyridine (N-serve) on nitrification and nitrous oxide (N₂O) emission from a Vertosol from southern Australia, under controlled moisture and temperature. Nitrification rates in the control soil were strongly influenced by the temperature and moisture, increasing by a factor of 3.6 for each 10 °C increase between 5 and 25 °C. DMPP inhibited nitrification effectively for 42 days at 5-15 °C and 40-60% water filled pore space (WFPS). DMPP also slowed nitrification appreciably at 25 °C when the soil was at 40% WFPS, but was less effective at 60% water filled pore space. N-serve inhibited nitrification effectively for 42 days under all test conditions. Emissions of N₂O from the urea treatment (no inhibitors) significantly increased with increasing temperature and moisture. The ratio of total N₂O emission to total nitrification was not constant and varied from around 0.03% at 5 °C and 40% WFPS to 0.12% at 25 °C and 60% WFPS. DMPP and N-serve reduced cumulative N₂O emission over 42 days by more than 65% under all the imposed conditions.     

农田土壤N2O排放的关键过程及影响因素

一氧化二氮 (N₂O) 作为重要的温室气体之一,在全球气候变化研究中引人关注。随着氮肥使用量的增加,农田土壤N₂O排放已经成为全球关注和研究的热点。人们普遍认为土壤硝化、反硝化过程是N₂O产生的两个主导途径,而诸如施肥、灌水等农田管理措施以及土壤pH、温度等环境因子均会影响农田土壤N₂O产生和排放。本文系统论述了土壤N₂O产生的各主要途径,并综述了氮源、碳源、水分含量、氧气含量、土壤pH和温度以及其他调控因子对N₂O排放的影响,旨在阐明各过程对N₂O排放的产生机制及主要环境因子的影响,以期为后续研究提供参考和理论依据。农田土壤硝化过程本身对N₂O排放的直接贡献较小,N₂O产生的主要来源是包含硝化细菌的反硝化、硝化–反硝化耦合作用在内的生物反硝化过程。真菌反硝化和化学反硝化在酸性土壤以及硝酸异化还原成铵过程在高有机质和厌氧土壤环境中对N₂O排放具有重要作用。未来研究可从农田土壤N₂O的产生和消耗机制、降低N₂O/N₂产物比、N₂O的还原过程及相关影响因素进行深入研究。此外,利用新技术方法,探究土壤物理、化学和生物学因素对氮素转化过程的影响,重点关注N₂O峰值排放及相关联微生物的响应,并构建土壤氮素平衡和N₂O排放模型,可进一步加深对农田土壤N₂O排放机制和影响因素的理解。     

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

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

Nitrous oxide production in turfgrass systems: Effects of soil properties and grass clipping recycling

Soil N₂O emissions can affect global environments because N₂O is a potent greenhouse gas and ozone depletion substance. In the context of global warming, there is increasing concern over the emissions of N₂O from turfgrass systems. It is possible that management practices could be tailored to reduce emissions, but this would require a better understanding of factors controlling N₂O production. In the present study we evaluated the spatial variability of soil N₂O production and its correlation with soil physical, chemical and microbial properties. The impacts of grass clipping addition on soil N₂O production were also examined. Soil samples were collected from a chronosequence of three golf courses (10, 30, and 100-year-old) and incubated for 60 days at either 60% or 90% water filled-pore space (WFPS) with or without the addition of grass clippings or wheat straw. Both soil N₂O flux and soil inorganic N were measured periodically throughout the incubation. For unamended soils, cumulative soil N₂O production during the incubation ranged from 75 to 972 ng N g⁻¹ soil at 60% WFPS and from 76 to 8842 ng N g⁻¹ soil at 90% WFPS. Among all the soil physical, chemical and microbial properties examined, soil N₂O production showed the largest spatial variability with the coefficient of variation ~110% and 207% for 60% and 90% WFPS, respectively. At 60% WFPS, soil N₂O production was positively correlated with soil clay fraction (Pearson's r = 0.91, P < 0.01) and soil NH₄⁺–N (Pearson's r = 0.82, P < 0.01). At 90% WFPS, however, soil N₂O production appeared to be positively related to total soil C and N, but negatively related to soil pH. Addition of grass clippings and wheat straw did not consistently affect soil N₂O production across moisture treatments. Soil N₂O production at 60% WFPS was enhanced by the addition of grass clippings and unaffected by wheat straw (P < 0.05). In contrast, soil N₂O production at 90% WFPS was inhibited by the addition of wheat straw and little influenced by glass clippings (P < 0.05), except for soil samples with >2.5% organic C. Net N mineralization in soil samples with >2.5% organic C was similar between the two moisture regimes, suggesting that O₂ availability was greater than expected from 90% WFPS. Nonetheless, small and moderate changes in the percentage of clay fraction, soil organic matter content, and soil pH were found to be associated with large variations in soil N₂O production. Our study suggested that managing soil acidity via liming could substantially control soil N₂O production in turfgrass systems.     

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

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

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.     

Abiotic dissolution and biological uptake of nitrous oxide in Mediterranean woodland and pasture soil

Soil is generally regarded as a net emitter of nitrous oxide (N₂O). However, there are numerous field studies showing net uptake of N₂O from soil in different ecosystems. Consumption of N₂O may be abiotic (absorption by water; adsorption by soil matrix) and biotic (microbial reduction of N₂O). This study is the first using undisturbed soil cores to determine the capacity of soil to consume N₂O and discuss the fate of N₂O.We exposed the base of undisturbed soil cores from Mediterranean pasture and woodland soil to elevated concentrations of N₂O and sulphur hexafluoride (SF₆; as tracer gas). Headspace concentrations of N₂O and SF₆ were determined over time and consumption rates of N₂O were calculated ranging from 148.8 ± 19.8 ng N₂O min⁻¹ g⁻¹ to 163.8 ± 17.2 ng N₂O min⁻¹ g⁻¹ in woodland soil and from 117.2 ± 36.1 ng N₂O min⁻¹ g⁻¹ to 145.1 ± 19.4 ng N₂O min⁻¹ g⁻¹ in pasture soil. Absorption of N₂O by soil water contributed 17–49% of the total N₂O consumption. The remaining N₂O consumed by the cores was due to adsorbtion by the soil matrix and/or reduction by microbes.Mediterranean soil from different ecosystems with different nitrogen (N) loads has a great potential to store and consume N₂O, if exposed to an N₂O elevated atmosphere.     

Effects of rate and depth of fertilizer application on emission of nitrous oxide from soil fertilized with anhydrous ammonia

Summary Field studies to determine the effect of different rates of fertilization on emission of nitrous oxide (N₂O) from soil fertilized with anhydrous ammonia showed that the fertilizer-induced emission of N₂O-N in 116 days increased from 1.22 to 4.09 kg ha^–1 as the rate of anhydrous ammonia N application was increased from 75 to 450 kg ha^–1. When expressed as a percentage of the N applied, the fertilizer-induced emission of N₂O-N in 116 days decreased from 1.6% to 0.9% as the rate of fertilizer N application was increased from 75 to 450 kg N ha^–1. The data obtained showed that a 100% increase in the rate of application of anhydrous ammonia led to about a 60% increase in the fertilizer-induced emission of N₂O.Field studies to determine the effect of depth of fertilizer injection on emission of N₂O from soil fertilized with anhydrous ammonia showed that the emission of N₂O-N in 156 days induced by injection of 112 kg anhydrous ammonia N ha^–1 at a depth of 30 cm was 107% and 21 % greater than those induced by injection of the same amount of N at depths of 10 cm and 20 cm, respectively. The effect of depth of application of anhydrous ammonia on emission of N₂O was less when this fertilizer was applied at a rate of 225 kg N ha^–1.     

Relationship between nitrifier and denitrifier community composition and abundance in predicting nitrous oxide emissions from ephemeral wetland soils

The link between differences in the community composition of nitrifiers and denitrifiers to differences in the emission of nitrous oxide (N₂O) from soils remains unclear. Nitrifier and denitrifier community composition, abundance and N₂O emission activity were determined for two common landscapes characteristic of the North American “prairie pothole region”: cultivated wetlands (CW) vs. uncultivated wetlands (UW). The hypotheses of this study were: (1) landscape selects for different nitrifier and denitrifier communities, (2) denitrification was the dominant N₂O emitting process, and (3) a relationship exists between nitrifier and denitrifier community composition, their abundance, and N₂O emission. Comparisons were made among soils from three CW and three UW at the St. Denis National Wildlife Area. Denaturing gradient gel electrophoresis was used to compare community composition, and quantitative polymerase chain reaction was used to estimate community size. Incubation experiments on re-packed soil cores with ¹⁵N-labeled nitrate were performed to assess the relative contributions of nitrification and denitrification to total N₂O emission. Results indicate: (1) nitrification was the primary source of N₂O emission, (2) cultivation increased nitrifier abundance but decreased nitrifier richness, (3) denitrifier abundance was not affected by cultivation but richness was increased by cultivation, and (4) differences in nitrifier and denitrifier communities composition and abundance between land-use and landform did not correspond to differences in N₂O emission.     

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

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

Effects of trampling of a wet dairy pasture soil on soil porosity and on mitigation of nitrous oxide emissions by a nitrification inhibitor,dicyandiamide

Urine patches in dairy pastures are major sources of nitrous oxide (N₂O). Wet winters result in compaction damage to pastures because of animal trampling. The nitrification inhibitor, dicyandiamide (DCD), is effective at reducing N₂O emissions from urine patches. Here, we assessed the extent of damage to the physical quality of the soil by trampling and whether this influenced the ability of DCD to mitigate N₂O emissions. A field experiment was conducted where a sandy loam soil was trampled by a mechanical hoof just before urine and DCD application. Trampling reduced air permeability and pore continuity, but this had no effect on bulk density. Urine appeared to have contributed to pore collapse and blockage. Trampling increased average cumulative N₂O emissions from 1.74 to 4.66% of urine‐N applied. This effect was attributed to increased water‐filled pore space, aggregate destruction and suppression of grass growth. DCD was highly effective in reducing N₂O emissions, with the N₂O emission factor of the urine‐N being decreased by 58–63%. Trampling did not significantly affect the effectiveness of DCD in reducing N₂O emissions.