Effect of long-term field exposure of soil to acetylene on nitrification,denitrification, and acetylene consumption

Coated CaC₂ is a newly developed product which can supply nitrification-inhibiting quantities of C₂H₂ (1–10 Pa) to the soil, throughout a cropping season. This method of applying C₂H₂ to the soil maintains C₂H₂ in the soil continuously for several months. It is not know whether these low C₂H₂ concentrations alter soil microbial processes. A field study was initiated to determine the effect of supplying C₂H₂ to a clay soil, using coated CaC₂, on soil respiration, denitrification, nitrification, and C₂H₂ consumption. The C₂H₂ consumption rate increased with length of soil exposure to C₂H₂ (r ²=0.59). The rates of CO₂ production (r ²=0.88) and denitrification (r ²=0.86) were both highly correlated with the C₂H₂ consumption rates. The nitrifier potential decreased to a minimum of 21% of the control after 3 months of C₂H₂ treatment. After this time, nitrifier activity increased to 41% of the control after 11 months of treatment. This increase was due to increased C₂H₂ consumption in the soil. After 3 months of continuous application of C₂H₂ to the soil, the C₂H₂ concentrations were generally below that necessary to inhibit nitrification. No adaptation to the C₂H₂ by nitrifiers was found. Repeating these measurements 1 year later showed that soils previously exposed to C₂H₂ retained their enhanced C₂H₂ oxidation capacity and the capacity to use C₂H₂ to increase denitrification. Nitrification potentials remained about 50% lower in soils exposed to C₂H₂ a year earlier compared to soils not previously exposed to C₂H₂.     

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.     

区分土壤中硝化与反硝化对N2O产生贡献的方法

土壤是产生N₂O的最主要来源之一。硝化和反硝化反应是产生N₂O的主要机理，由于硝化和反硝化微生物同时存在于土壤中，因而硝化和反硝化作用能同时产生N₂O。N₂O的来源可通过使用选择性抑制剂，杀菌剂以及加入的标记底物确定。通过对生成N₂O反应的每一步分析，主要从抑制反应发生的催化酶和细菌着手，总结了测量区分硝化、反硝化和DNRA反应对N₂O产生的贡献方法。并对¹⁵N标记底物法，乙炔抑制法和环境因子抑制法作了详细介绍。     

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.     

Gaseous and leaching nitrogen losses from no-tillage and conventional tillage systems following surface application of cattle manure

Previous studies have demonstrated inconsistent results on the impact of tillage systems on nitrogen (N) losses from field-applied manure. This study assessed the impact of no-tillage (NT) and conventional tillage (CT) systems on gaseous N losses, N₂O:N₂O + N₂ ratios and NO₃⁻-N leaching following surface application of cattle manure. The study was undertaken during the 2003/2004 and 2004/2005 seasons at two field sites in Nova Scotia namely, Streets Ridge (SR) in Cumberland County and the Bio-environmental Engineering Centre (BEEC) in Truro. Results showed that the NT system had higher (p < 0.05) NH₃ losses than CT. Over the two seasons, manure incorporation in CT reduced NH₃ losses on average by 86% at SR and 78% at BEEC relative to NT. At both sites and during both seasons, denitrification rates and N₂O fluxes in NT were generally higher than in CT plots, presumably due to higher soil water and organic matter content in NT. Over the two seasons, mean denitrification rates at SR were 239 and 119 g N ha⁻¹ d⁻¹, while N₂O fluxes were 120 and 64 g N ha⁻¹ d⁻¹ under NT and CT, respectively. At BEEC mean denitrification rates were 114 and 71 g N ha⁻¹ d⁻¹, while N₂O fluxes were 52 and 27 g N ha⁻¹ d⁻¹ under NT and CT, respectively. Conversely, N₂O:N₂O + N₂ ratios were lower in NT than CT suggesting more complete reduction of N₂O to N₂ under NT. When averaged across all soil depths, NO₃⁻-N was higher (p < 0.05) in CT than NT. Nitrate-N decreased with depth at both sites regardless of tillage. In most cases, NO₃⁻-N was higher under CT than NT at all soil depths. Similarly, flow-weighted average NO₃⁻-N concentrations in drainage water were generally higher under CT. This may be partly attributed to higher denitrification rates under NT. Therefore, NT may be a viable strategy to remove NO₃⁻-N from the soil, and thus, reduce NO₃⁻-N contamination of groundwater. However, it should be noted that while the use of NT reduces NO₃⁻-N leaching it may come with unintended environmental tradeoffs, including increased NH₃ and N₂O emissions.     

The effect of some carbon substrates on denitrification rates and carbon utilization in soil

Summary Soil was amended with a variety of carbon sources, including four soluble compounds (glucose, sucrose, glycerol and mannitol) and two plant residues (straw and alfalfa).. Potential denitrification rates, measured both as N₂O accumulation and NO₃ ^– disappearance, were compared, and the predicted values of available C, measured as CO₂ production and water-extractable C, were assessed.The two measures of denitrification agreed well although N₂O accumulation was, found to be most sensitive. Soil treated with the four soluble C compounds resulted in the same rate of denitrification although glycerol was not as rapidly oxidized. Alfalfa-amended soil produced a significantly higher rate of denitrification than the same amount of added straw. CO₂ evolution was found to be a good predictor of denitrification over the first 2 days of sampling, but neither measure of available substrate C correlated well with denitrification rate beyond 4 days, when NO₃ ^– was depleted in most treatments. The data with alfalfa-amended soil suggested that denitrifiers used water-extractable C. materials produced by other organisms under anaerobic conditions.     

施肥对夏玉米季紫色土N2O排放及反硝化作用的影响

采用原状土柱-乙炔抑制培养法研究了施肥对紫色土玉米生长季土壤N2O排放通量和反硝化作用的影响.结果表明:玉米季施肥显著增加土壤N2O排放和反硝化损失,同时,各施肥处理间N2O排放与反硝化损失量差异显著.猪厩肥、猪厩肥配施氮磷钾肥、氮肥、氮磷钾肥和秸秆配施氮磷钾肥等处理的土壤N,O排放量分别为3.01、2.86、2.51、2.19和1.88 kg hm-2,分别占当季氮肥施用量的1.63％、1.53％、1.30％、1.09％和0.88％,反硝化损失量分别为6.74、6.11、5.23、4.69和4.12 kg hm-2,分别占当季氮肥施用量的3.97％、3.55％、2.97％、2.61％和2.23％,不施肥土壤的N2O排放量和反硝化损失量仅为0.56和0.78 kg hm-2.施肥是紫色土玉米生长前期(2周内)土壤N2O排放和反硝化速率出现高峰的主要驱动因子,土壤铵态氮和硝态氮含量是影响土壤N2O排放、土壤硝化和反硝化作用的限制因子,土壤含水量是重要影响因子,降雨是主要促发因素.土壤N2O排放量与反硝化损失量的比值介于0.45 ～0.72之间,土壤反硝化损失量极显著高于土壤N2O排放量,说明土壤反硝化作用是紫色土玉米生长季氮肥损失的重要途径.     

N2O emissions and product ratios of nitrification and denitrification as affected by freezing and thawing

Agricultural soils contribute significantly to atmospheric nitrous oxide (N₂O). A considerable part of the annual N₂O emission may occur during the cold season, possibly supported by high product ratios in denitrification (N₂O/(N₂+N₂O)) and nitrification (N₂O-N/(NO₃⁻-N+NO₂⁻-N)) at low temperatures and/or in response to freeze-thaw perturbation. Water-soluble organic materials released from frost-sensitive catch crops and green manure may further increase winter emissions. We conducted short-term laboratory incubations under standardized moisture and oxygen (O₂) conditions, using nitrogen (N) tracers (¹⁵N) to determine process rates and sources of emitted N₂O after freeze-thaw treatment of soil or after addition of freeze-thaw extract from clover. Soil respiration and N₂O production was stimulated by freeze-thaw or addition of plant extract. The N₂O emission response was inversely related to O₂ concentration, indicating denitrification as the quantitatively prevailing process. Denitrification product ratios in the two studied soils (pH 4.5 and 7.0) remained largely unaltered by freeze-thaw or freeze-thaw-released plant material, refuting the hypothesis that high winter emissions are due to frost damage of N₂O reductase activity. Nitrification rates estimated by nitrate (NO₃⁻) pool enrichment were 1.5-1.8 μg NO₃-N g⁻¹ dw soil d⁻¹ in freeze-thaw-treated soil when incubated at O₂ concentrations above 2.3 vol% and one order of magnitude lower at 0.8 vol% O₂. Thus, the experiments captured a situation with severely O₂-limited nitrification. As expected, the O₂ stress at 0.8 vol% resulted in a high nitrification product ratio (0.3 g g⁻¹). Despite this high product ratio, only 4.4% of the measured N₂O accumulation originated from nitrification, reaffirming that denitrification was the main N₂O source at the various tested O₂ concentrations in freeze-thaw-affected soil. N₂O emission response to both freeze-thaw and plant extract addition appeared strongly linked to stimulation of carbon (C) respiration, suggesting that freeze-thaw-induced release of decomposable organic C was the major driving force for N₂O emissions in our soils, both by fuelling denitrifiers and by depleting O₂. The soluble C (applied as plant extract) necessary to induce a CO₂ and N₂O production rate comparable with that of freeze-thaw was 20-30 μg C g⁻¹ soil dw. This is in the range of estimates for over-winter soluble C loss from catch crops and green manure plots reported in the literature. Thus, freeze-thaw-released organic C from plants may play a significant role in freeze-thaw-related N₂O emissions.     

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.     

Factors regulating acetylene reduction assay for measuring heterotrophic nitrogen fixation in water-logged soils

In the C₂H₂-C₂H₄ assay for measurement of heterotrophic N₂ fixation in water-logged soils, the diffusion of C₂H₂ into the soil and the recovery of C₂H₄ from it are critical factors regulating the assay result. To establish an C₂H₂-C₂H₄ assay technique suitable for waterlogged soils, the C₂H₂-reducing activities (ARA), assayed by varying the method of assay gas filling, the pC₂H₂ of the assay gas, the duration of assay incubation and of soil vibration before the gas sampling, were compared.

A maximum ARA was measured when the following set of procedures were applied to the soil sample in assay flasks: 1) a 4-fold repetition of I-min evacuation under 0.01 atmospheric pressure and the subsequent I-min filling under 1 atmospheric pressure with assay gas at pC₂H₂ of 0.1 atm, 2) an assay incubation for 3 hr, and 3) a sampling of an aliquot of the headspace gas after strongly vibrating the flask for 1 min.

The ARA measured by this technique was several times larger than those measured by the techniques hitherto applied, and corresponded to an almost 80% of the V _max of the sample. This technique was, therefore, proposed for the assay of heterotrophic N₂ fixation in waterlogged soils.

A striking depression of ARA in the soil sample prepared with agitation indicated that a microbial ecosystem established in the soil should be kept as undisturbed as possible throughout the C₂H₂-C₂H₄ assay.     

Phytotron studies to compare nitrogen losses from corn-planted soil by the 15-N balance or direct dinitrogen and nitrous oxide measurements

Summary Containers filled with soil mixed with potassium nitrate highly enriched in ¹⁵N were planted with corn (Zea mays L.) and kept in a phytotron under controlled conditions for 79 days. Soil water content was normally maintained at exactly 60% water-holding capacity (–33 kPa), but it was increased several times to 85% (–5 kPa) for short periods to favour denitrification. The soil headspace was sealed from the phytotron atmosphere and aerated by a continuous stream of air. Nitrous oxide emission was measured by estimating the N₂O concentration differences in the air entering and leaving the containers. Emission of N₂ was estimated by mass spectroscopy from changes in the N₂ composition in the temporarily enclosed soil headspace. Both methods were carefully checked for accuracy by different tests. At specific times during the experiment the distribution of ¹⁵N between plants and soil was determined and a ¹⁵N balance established. Emission of N gases peaked at times of increased water content and reached maxima of 149 and 142 g N pot^–1 day^–1 for N₂O and N₂, respectively. While N losses of 5% ± 2% were indicated by the ¹⁵N balance, only 1.1% ± 0.3% loss from 2.7 g applied N was estimated from the N₂O and N₂ measurements after 79 days. Possible reasons for these differences are discussed.     

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

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

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.     

华北平原水浇玉米-小麦轮作农田氨挥发与反硝化损失

Ammonia (NH3) volatilization, denitriflcation loss, and nitrous oxide (N2O) emission were investigated from an irrigated wheat-maize rotation field on the North China Plain, and the magnitude of gaseous N loss from denitrification and NH3 volatilization was assessed. The micrometeorological gradient diffusion method in conjunction with a Bowen Ratio system was utilized to measure actual NH3 fluxes over a large area, while the acetylene inhibition technique (intact soil cores) was employed for measurement of denitrification losses and N2O emissions. Ammonia volatilization loss was 26.62% of the applied fertilizer nitrogen (N) under maize, while 0.90% and 15.55% were lost from the wheat field at sowing and topdressing, respectively. The differences in NH3 volatilization between different measurement events may be due to differences between the fertilization methods, and to differences in climatic conditions such as soil temperature. Denitrification losses in the fertilized plots were 0.67%-2.87% and 0.31%-0.49% of the applied fertilizer N under maize and wheat after subtracting those of the controls, respectively. Nitrous oxide emissions in the fertilized plots were approximately 0.08%-0.41% and 0.26%-0.34% of the applied fertilizer N over the maize and wheat seasons after subtracting those of the controls, correspondingly. The fertilizer N losses due to NH3 volatilization were markedly higher than those through denitriflcation and nitrous oxide emissions. These results indicated that NH3 volatilization was an important N transformation in the crop-soil system and was likely to be the major cause of low efficiencies with N fertilizer in the study area. Denitriflcation was not a very important pathway of N fertilizer loss, but did result in important evolution of the greenhouse gas N2O and the effect of N2O emitted from agricultural fields on environment should not be overlooked.     

Compared effects of long-term pig slurry applications and mineral fertilization on soil denitrification and its end products (N2O, N2)

The long-term (9 years) effect of pig slurry applications vs mineral fertilization on denitrifying activity, N₂O production and soil organic carbon (C) (extractable C, microbial biomass C and total organic C) was compared at three soil depths of adjacent plots. The denitrifying activities were measured on undisturbed soil cores and on sieved soil samples with acetylene method to estimate denitrification rates under field or potential conditions. Pig slurry applications had a moderate impact on the C pools. Total organic C was increased by +6.5% and microbial biomass C by ≥25%. The potential denitrifying activity on soil suspension was stimulated (×1.8, P<0.05) 12 days after the last slurry application. This stimulation was still apparent, but not significant, 10 months later and, according to both methods of denitrifying activity measurement (r ²=0.916, P<0.01 on sieved soil; r ²=0.845, P<0.001 on soil cores), was associated with an increase in microbial biomass C above a threshold of about 105 mg kg⁻¹. The effect of pig slurry on denitrification and N₂O reduction rates was detected on the surface layer (0–20 cm) only. However, no pig slurry effect could be detected on soil cores at field conditions or after NO₃ ⁻ enrichments at 20°C. Although the potential denitrifying activity in sieved soil samples was stimulated, the N₂O production was lower (P<0.03) in the plot fertilized with pig slurry, indicating a lower N₂O/(N₂O + N₂) ratio of the released gases. The pig-slurry-fertilized plot also showed a higher N₂O reduction activity, which is coherent with the lower N₂O production in anaerobiosis.     

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

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

Variations in the rates of nitrification and denitrification during the growth of potatoes (Solanum tuberosum L.) in soil with different carbon inputs and the effect of these inputs on soil nitrogen and plant yield

Summary A potato crop (Solanum tuberosum L. cv. Maris piper) was grown in a soil to which N was added, as NH₄NO₃, with or without added C, as sucrose or straw. Shortly after amendment the soil, in all treatments, contained only relatively low levels of mineral N. However, these levels increased later. The increase, which was greatest in the absence of added C and least with added sucrose, occurred before the emergence of the plant canopy. The addition of C to the soil had no effect on plant yield, measured either as dry matter or total N content. The potential nitrification rate was high early in the season, and decreased significantly as the plants developed. The potential denitrification rate showed two significant peaks in activity, possibly related to plant development, the first to the development of new roots and the second to root senescence. It seems probable that the amount of C released by the potato plants was only about one-quarter of that required for the maximum microbial activity.     

施氮及添加硝化抑制剂对苜蓿草地N2O排放的影响

为探究旱作紫花苜蓿(MedicagosativaL.)栽培草地氧化亚氮(N_2O)排放对施氮水平及添加硝化抑制剂的响应特征,采用传统静态箱法研究了不同施氮水平[0kg(N)·hm~(-2)(N0)、 50kg(N)·hm~(-2)(N50)、 100kg(N)·hm~(-2)(N100)和150kg(N)·hm~(-2)(N150)]以及添加硝化抑制剂双氰胺(DCD)150kg(N)·hm~(-2)(N150+DCD)对陇东苜蓿草地N_2O排放特征的影响。结果显示,监测期内N0、N50、N100和N150处理N_2O平均排放速率分别为3.5μg·m~(-2)·h~(-1)、4.1μg·m~(-2)·h~(-1)、5.0μg·m~(-2)·h~(-1)和6.1μg·m~(-2)·h~(-1),随着施氮梯度的增加, N_2O排放速率呈增加趋势。添加硝化抑制剂DCD对N_2O排放产生明显的抑制作用。与N150处理相比, N150+DCD处理下苜蓿草地N_2O平均排放速率下降50.7%, N_2O累计排放量显著降低61.6%(P0.05)。施氮对苜蓿产量没有显著影响,而N0、N50、N100和N150处理下单位苜蓿产量N_2O排放量随氮肥梯度的增加而增加,各处理分别为6.5 mg·kg~(-1)、7.8 mg·kg~(-1)、11.3 mg·kg~(-1)和12.5 mg·kg~(-1)。N_2O排放受土壤含水量影响深刻,生长季N_2O排放通量与土壤水分呈显著正相关关系(P0.05),而与土壤温度无显著相关性(P0.05)。综上,旱作紫花苜蓿栽培草地N_2O排放通量随施氮水平的增加明显增加,在相同施氮水平下添加硝化抑制剂DCD能显著抑制N_2O排放。相关研究结果对于该区域苜蓿草地合理施肥以及N_2O减排具有一定的实践指导意义。     

盐碱土壤N2O排放与amoA和narG功能基因丰度的响应规律

为揭示盐碱土壤中参与氨氧化过程和硝酸盐还原过程的amoA和narG基因丰度与N_2O排放的响应规律,本研究选取内蒙古河套灌区3种不同盐碱程度土壤(轻度盐土SA、强度盐土SB和盐土SC),通过控制室内温度和土壤质量含水量进行室内培养试验,并运用荧光定量PCR(real-time PCR)技术研究了盐碱土壤中N_2O排放速率、氨氧化细菌和narG(膜结合型硝酸还原酶)型反硝化细菌丰度与土壤环境因子之间的偶联关系。结果表明:SA、SB和SC3种盐碱土壤中,N_2O平均排放速率随着土壤盐碱程度的升高而升高,值分别为16.9、30.8、69.6μg/(kg·d);氨氧化细菌和narG型反硝化细菌丰度分别为0.415×10~4、6.91×10~4、9.44×10~4 copies和2.61×10~4、5.36×10~4、13.5×10~4 copies,表明在一定盐分条件下,土壤中的盐分能够促进氨氧化细菌和narG型反硝化细菌丰度。RDA分析结果显示,N2O平均排放速率与氨氧化细菌和narG型反硝化细菌丰度具有显著的正相关(r=0.863、0.975,P0.01);土壤pH、EC、速效钾和有机碳是盐碱土壤中影响N2O排放速率的主要环境因子,其中,土壤pH、EC、速效钾和N_2O排放速率存在显著正相关(r=0.968、0.983、0.987,P0.01),土壤有机碳和N_2O排放速率存在负相关(r=–0.800,P0.05),土壤有效磷和总氮与N_2O排放速率的相关性未达到显著水平(P0.05)。