Emission of N2O, N2 and CO2 from soil fertilized with nitrate: effect of compaction, soil moisture and rewetting

Soil compaction and soil moisture are important factors influencing denitrification and N₂O emission from fertilized soils. We analyzed the combined effects of these factors on the emission of N₂O, N₂ and CO₂ from undisturbed soil cores fertilized with (150 kg N ha⁻¹) in a laboratory experiment. The soil cores were collected from differently compacted areas in a potato field, i.e. the ridges (ρ_D=1.03 g cm⁻³), the interrow area (ρ_D=1.24 g cm⁻³), and the tractor compacted interrow area (ρ_D=1.64 g cm⁻³), and adjusted to constant soil moisture levels between 40 and 98% water-filled pore space (WFPS).High N₂O emissions were a result of denitrification and occurred at a WFPS≥70% in all compaction treatments. N₂ production occurred only at the highest soil moisture level (≥90% WFPS) but it was considerably smaller than the N₂O-N emission in most cases. There was no soil moisture effect on CO₂ emission from the differently compacted soils with the exception of the highest soil moisture level (98% WFPS) of the tractor-compacted soil in which soil respiration was significantly reduced. The maximum N₂O emission rates from all treatments occurred after rewetting of dry soil. This rewetting effect increased with the amount of water added. The results show the importance of increased carbon availability and associated respiratory O₂ consumption induced by soil drying and rewetting for the emissions of N₂O.     

Elevated CO2 concentration and nitrogen fertilisation effects on N2O and CH4 fluxes and biomass production of Phleum pratense on farmed peat soil

The effects of elevated CO₂ supply on N₂O and CH₄ fluxes and biomass production of Phleum pratense were studied in a greenhouse experiment. Three sets of 12 farmed peat soil mesocosms (10 cm dia, 47 cm long) sown with P. pratense and equally distributed in four thermo-controlled greenhouses were fertilised with a commercial fertiliser in order to add 2, 6 or 10 g N m⁻². In two of the greenhouses, CO₂ concentration was kept at atmospheric concentration (360 μmol mol⁻¹) and in the other two at doubled concentration (720 μmol mol⁻¹). Soil temperature was kept at 15 °C and air temperature at 20 °C. Natural lighting was supported by artificial light and deionized water was used to regulate soil moisture. Forage was harvested and the plants fertilised three times during the basic experiment, followed by an extra fertilisations and harvests. At the end of the experiment CH₄ production and CH₄ oxidation potentials were determined; roots were collected and the biomass was determined. From the three first harvests the amount of total N in the aboveground biomass was determined. N₂O and CH₄ exchange was monitored using a closed chamber technique and a gas chromatograph. The highest N₂O fluxes (on average, 255 μg N₂O m⁻² h⁻¹ during period IV) occurred just after fertilisation at high water contents, and especially at the beginning of the growing season (on average, 490 μg N₂O m⁻² h⁻¹ during period I) when the competition of vegetation for N was low. CH₄ fluxes were negligible throughout the experiment, and for all treatments the production and oxidation potentials of CH₄ were inconsequential. Especially at the highest rates of fertilisation, the elevated supply of CO₂ increased above- and below-ground biomass production, but both at the highest and lowest rates of fertilisation, decreased the total amount of N in the aboveground dry biomass. N₂O fluxes tended to be higher under doubled CO₂ concentrations, indicating that increasing atmospheric CO₂ concentration may affect N and C dynamics in farmed peat soil.     

Short-term effects of clearfelling on soil CO2, CH4, and N2O fluxes in a Sitka spruce plantation

We examined the effects of forest clearfelling on the fluxes of soil CO₂, CH₄, and N₂O in a Sitka spruce (Picea sitchensis (Bong.) Carr.) plantation on an organic-rich peaty gley soil, in Northern England. Soil CO₂, CH₄, N₂O as well as environmental factors such as soil temperature, soil water content, and depth to the water table were recorded in two mature stands for one growing season, at the end of which one of the two stands was felled and one was left as control. Monitoring of the same parameters continued thereafter for a second growing season. For the first 10 months after clearfelling, there was a significant decrease in soil CO₂ efflux, with an average efflux rate of 4.0 g m⁻² d⁻¹ in the mature stand (40-year) and 2.7 g m⁻² d⁻¹ in clearfelled site (CF). Clearfelling turned the soil from a sink (−0.37 mg m⁻² d⁻¹) for CH₄ to a net source (2.01 mg m⁻² d⁻¹). For the same period, soil N₂O fluxes averaged 0.57 mg m⁻² d⁻¹ in the CF and 0.23 mg m⁻² d⁻¹ in the 40-year stand. Clearfelling affected environmental factors and lead to higher daily soil temperatures during the summer period, while it caused an increase in the soil water content and a rise in the water table depth. Despite clearfelling, CO₂ remained the dominant greenhouse gas in terms of its greenhouse warming potential.     

Soil CO2 evolution: Response from arginine additions

Short-term response of soil C mineralization following drying/rewetting has been proposed as an indicator of soil microbial activity. Houston Black clay was amended with four rates of arginine to vary microbial responses and keep other soil properties constant. The evolution of CO₂ during 1 and 3 days following rewetting of dried soil was highly related to CO₂ evolution during 10 days following chloroform fumigation (r² = 0.92 and 0.93, respectively) which is a widely used method for soil microbial biomass C, which disrupts cellular membranes. This study suggest that the release of CO₂ following rewetting of dried soil with no amendments other than heat and water can be highly indicative of soil microbial activity and possibly be used as a quantitative measurement of soil biological quality in Houston Black soils.     

Elevated CO2 stimulates N2O emissions in permanent grassland

To evaluate climate forcing under increasing atmospheric CO₂ concentrations, feedback effects on greenhouse gases such as nitrous oxide (N₂O) with a high global warming potential should be taken into account. This requires long-term N₂O flux measurements because responses to elevated CO₂ may vary throughout annual courses. Here, we present an almost 9 year long continuous N₂O flux data set from a free air carbon dioxide enrichment (FACE) study on an old, N-limited temperate grassland. Prior to the FACE start, N₂O emissions were not different between plots that were later under ambient (A) and elevated (E) CO₂ treatments, respectively. However, over the entire experimental period (May 1998–December 2006), N₂O emissions more than doubled under elevated CO₂ (0.90 vs. 2.07 kg N₂O-N ha⁻¹ y⁻¹ under A and E, respectively). The strongest stimulation occurred during vegetative growth periods in the summer when soil mineral N concentrations were low. This was surprising because based on literature we had expected the highest stimulation of N₂O emissions due to elevated CO₂ when mineral N concentrations were above background values (e.g. shortly after N application in spring). N₂O emissions under elevated CO₂ were moderately stimulated during late autumn–winter, including freeze–thaw cycles which occurred in the 8th winter of the experiment. Averaged over the entire experiment, the additional N₂O emissions caused by elevated CO₂ equaled 4738 kg CO₂-equivalents ha⁻¹, corresponding to more than half a ton (546 kg) of CO₂ ha⁻¹ which has to be sequestered annually to balance the CO₂-induced N₂O emissions. Without a concomitant increase in C sequestration under rising atmospheric CO₂ concentrations, temperate grasslands may be converted into greenhouse gas sources by a positive feedback on N₂O emissions. Our results underline the need to include continuous N₂O flux measurements in ecosystem-scale CO₂ enrichment experiments.     

Can a mixed stand of N2-fixing and non-fixing plants restrict N2O emissions with increasing CO2 concentration?

Initial effects of elevated atmospheric CO₂ concentration on N₂O fluxes and biomass production of timothy/red clover were studied in the laboratory. The experimental design consisted of two levels of atmospheric CO₂ (ca. 360 and 720 μmol CO₂ mol⁻¹) and two N fertilisation levels (5 and 10 g N m⁻²). There was a total of 36 mesocosms comprising sandy loam soil, which were equally distributed in four thermo-controlled greenhouses. In two of the greenhouses, the CO₂ concentration was kept at ambient concentration and in the other two at doubled concentration. Forage was harvested and the plants fertilised three times during the basic experiment, followed by harvest, a fertilisation with the double amount of nitrogen and rise of water level. Under elevated CO₂, harvestable and total aboveground dry biomass production of a mixed Trifolium/Phleum stand was increased at both N treatments compared to ambient CO₂. The N₂O flux rates under ambient CO₂ were significantly higher at both N treatments during the early growth of mixed Phleum/Trifolium mesocosms compared to the N₂O flux rate under elevated CO₂. However, when the conditions were favourable for denitrification at the end of the experiment, i.e. N availability and soil moisture were high enough, the elevated CO₂ concentration enhanced the N₂O efflux.     

Factors controlling soil CO2 effluxes and the effects of rewetting on effluxes in adjacent deciduous, coniferous, and mixed forests in Korea

To better understand the factors that control forest soil CO₂ efflux and the effects of rewetting on efflux, we measured soil CO₂ efflux in adjacent deciduous, coniferous, and mixed forests in the central part of the Korean Peninsula over the course of one year. We also conducted laboratory rewetting experiments with soil collected from the three sites using three different incubation temperatures (4 °C, 10 °C, and 20 °C). Soil moisture (SM), soil organic matter (SOM), and total root mass values of the three sites were significantly different from one another; however, soil temperature (ST), observed soil CO₂ efflux and sensitivity of soil CO₂ efflux to ST (i.e., Q₁₀ = 3.7 ± 0.1) were not significantly different among the three sites. Soil temperature was a dominant control factor regulating soil CO₂ efflux during most of the year. We infer that soil CO₂ efflux was not significantly different among the sites due to similar ST and Q₁₀. Though a significant increase in soil CO₂ efflux following rewetting of dry soil was observed both in the field observations (60-170%) and laboratory incubation experiments (100-1000%), both the increased rates of soil CO₂ efflux and the magnitude of change in SM were not significantly different among the sites. The increased rates of soil CO₂ efflux following rewetting depended on the initial SM before rewetting. During drying phase after rewetting, a significant correlation between SM and soil CO₂ efflux was found, but the effect of ST on increased soil CO₂ efflux was not clear. Cumulative peak soil CO₂ efflux (11.3 ± 0.7 g CO₂ m⁻²) following rewetting in the field was not significantly different among the sites. Those evidences indicate that the observed similar rewetting effects on soil CO₂ efflux can be explained by the similar magnitude of change in SM after rewetting at the sites. We conclude that regardless of vegetation type, soil CO₂ efflux and the effect of rewetting on soil CO₂ efflux do not differ among the sites, and ST is a primary control factor for soil CO₂ efflux while SM modulates the effect of rewetting on soil CO₂ efflux. Further studies are needed to quantify and incorporate relationship of initial dryness of the soil and the frequency of the dry-wet cycle on soil CO₂ efflux into models describing carbon (C) processes in forested ecosystems.     

Tillage effects on N2O emissions as influenced by a winter cover crop

Conservation tillage practices are widely used to protect against soil erosion and soil C losses, whereas winter cover crops are used mainly to protect against N losses during autumn and winter. For the greenhouse gas balance of a cropping system the effect of reduced tillage and cover crops on N₂O emissions may be more important than the effect on soil C. This study monitored emissions of N₂O between September 2008 and May 2009 in three tillage treatments, i.e., conventional tillage (CT), reduced tillage (RT) and direct drilling (DD), all with (+CC) or without (−CC) fodder radish as a winter cover crop. Cover crop growth, soil mineral N dynamics, and other soil characteristics were recorded. Furthermore, soil concentrations of N₂O were determined eight times during the monitoring period using permanently installed needles. There was little evidence for effects of the cover crop on soil mineral N. Following spring tillage and slurry application soil mineral N was dominated by the input from slurry. Nitrous oxide emissions during autumn, winter and early spring remained low, although higher emissions from +CC treatments were indicated after freezing events. Following spring tillage and slurry application by direct injection N₂O emissions were stimulated in all tillage treatments, reaching 250-400 μg N m⁻² h⁻¹ except in the CT + CC treatment, where emissions peaked at 900 μg N m⁻² h⁻¹. Accumulated emissions ranged from 1.6 to 3.9 kg N₂O ha⁻¹. A strong positive interaction between cover crop and tillage was observed. Soil concentration profiles of N₂O showed a significant accumulation of N₂O in CT relative to RT and DD treatments after spring tillage and slurry application, and a positive interaction between slurry and cover crop residues. A comparison in early May of N₂O emissions with flux estimates based on soil concentration profiles indicated that much of the N₂O emitted was produced near the soil surface.     

Effects of C and N availability and soil-water potential interactions on N2O evolution and PLFA composition

Mitigation of agricultural N₂O emissions via management requires quantitative information about the regulation of the underlying processes. In this laboratory study, short-term evolution of N₂O from repacked soil was determined using an arable sandy loam soil adjusted to three water potentials (−15, −30 or −100 hPa) that were reached by adjustment of partly air-dried soil with nutrient solutions or water; a water retention curve of repacked soil had been determined prior to the incubation experiment. The amendments included a control treatment receiving water (CTL), and aqueous solutions of carbon in the form of glucose (C), ammonium sulfate (N), or both (CN). Rates of CO₂ and N₂O evolution were followed during 14 days. Soil inorganic N and phospholipid fatty acid (PLFA) composition were analyzed by the end of incubation. Across all nutrient treatments, the soil at the lower moisture content (−100 hPa) showed little or no N₂O evolution irrespective of nutrient treatment. Adding glucose alone reduced N₂O evolution relative to CTL. The addition of N alone had no effect on soil respiration, but significantly increased nitrate accumulation and N₂O evolution. The CN treatment resulted in higher respiration than with C amendment alone, but less N₂O evolution than with N alone, at least at −15 and −30 hPa. Whole-soil PLFA fingerprints at the end of incubation reflected the complex response of gaseous emissions. At −15 hPa growth of Gram negative bacteria, probably including denitrifiers, in the CN treatment was indicated by low cyclopropane-to-precursor ratios. At −100 hPa differentiation of branched-chain fatty acids was taken as evidence for an effect of C amendment on Gram positive bacteria. The highest potential for N₂O evolution was observed at the intermediate soil wetness level; the corresponding gas diffusivities indicated that this parameter may be a better predictor of N₂O emissions than water-filled pore space.     

The N2O product ratio of nitrification and its dependence on long-term changes in soil pH

The contribution of nitrification to the emission of nitrous oxide (N₂O) from soils may be large, but its regulation is not well understood. The soil pH appears to play a central role for controlling N₂O emissions from soil, partly by affecting the N₂O product ratios of both denitrification (N₂O/(N₂+N₂O)) and nitrification (N₂O/(NO₂⁻+NO₃⁻). Mechanisms responsible for apparently high N₂O product ratios of nitrification in acid soils are uncertain. We have investigated the pH regulation of the N₂O product ratio of nitrification in a series of experiments with slurries of soils from long-term liming experiments, spanning a pH range from 4.1 to 7.8. ¹⁵N labelled nitrate (NO₃⁻) was added to assess nitrification rates by pool dilution and to distinguish between N₂O from NO₃⁻ reduction and NH₃ oxidation. Sterilized soil slurries were used to determine the rates of chemodenitrification (i.e. the production of nitric oxide (NO) and N₂O from the chemical decomposition of nitrite (NO₂⁻)) as a function of NO₂⁻ concentrations. Additions of NO₂⁻ to aerobic soil slurries (with ¹⁵N labelled NO₃⁻ added) were used to assess its potential for inducing denitrification at aerobic conditions. For soils with pH?5, we found that the N₂O product ratios for nitrification were low (0.2-0.9‰) and comparable to values found in pure cultures of ammonia-oxidizing bacteria. In mineral soils we found only a minor increase in the N₂O product ratio with increasing soil pH, but the effect was so weak that it justifies a constant N₂O product ratio of nitrification for N₂O emission models. For the soils with pH 4.1 and 4.2, the apparent N₂O product ratio of nitrification was 2 orders of magnitude higher than above pH 5 (76‰ and 14‰). This could partly be accounted for by the rates of chemodenitrification of NO₂⁻. We further found convincing evidence for NO₂⁻-induction of aerobic denitrification in acid soils. The study underlines the role of NO₂⁻, both for regulating denitrification and for the apparent nitrifier-derived N₂O emission.     

Microbial activity and bacterial composition of H2-treated soils with net CO2 fixation

The effects of H₂ gas treatment of an agricultural soil cultivated previously with a mixture of clover (Trifolium pratense) and alfalfa (Medicago sativa) on CO₂ dynamics and microbial activity and composition were analyzed. The H₂ emission rate of 250 nmol H₂ g⁻¹ soil h⁻¹ was similar to the upper limit of estimated H₂ amounts emitted from N₂ fixing nodules into the surrounding soil ([Dong, Z., Layzell, D.B., 2001. H₂ oxidation, O₂ uptake and CO₂ fixation in hydrogen treated soil. Plant and Soil 229, 1-12.]). After 1 week of H₂ supply to soil samples simultaneously with H₂ uptake net CO₂ production declined continuously and this finally led to a net CO₂ fixation rate in the H₂-treated soil of 8 nmol CO₂ g⁻¹ soil h⁻¹. The time course of H₂ uptake and CO₂ fixation in the soils corresponded with an increase in microbial activity and biomass of the H₂-treated soil determined by microcalorimetric measurements, fluorescence in situ hybridization analysis (FISH) and DNA staining (DAPI). Shifts in the bacterial community structure caused by the supply of H₂ were recorded. While the H₂ treatment stimulated β-and γ-subclasses of Proteobacteria, it had no significant effect on α-Proteobacteria. In addition, FISH-detectable bacteria of the Cytophaga-Flavobacterium-Bacteroides phylum increased in numbers.     

Relationship between soil CO2 concentrations and forest-floor CO2 effluxes

To better understand the biotic and abiotic factors that control soil CO₂ efflux, we compared seasonal and diurnal variations in simultaneously measured forest-floor CO₂ effluxes and soil CO₂ concentration profiles in a 54-year-old Douglas fir forest on the east coast of Vancouver Island. We used small solid-state infrared CO₂ sensors for long-term continuous real-time measurement of CO₂ concentrations at different depths, and measured half-hourly soil CO₂ effluxes with an automated non-steady-state chamber. We describe a simple steady-state method to measure CO₂ diffusivity in undisturbed soil cores. The method accounts for the CO₂ production in the soil and uses an analytical solution to the diffusion equation. The diffusivity was related to air-filled porosity by a power law function, which was independent of soil depth. CO₂ concentration at all depths increased with increase in soil temperature, likely due to a rise in CO₂ production, and with increase in soil water content due to decreased diffusivity or increased CO₂ production or both. It also increased with soil depth reaching almost 10 mmol mol⁻¹ at the 50-cm depth. Annually, soil CO₂ efflux was best described by an exponential function of soil temperature at the 5-cm depth, with the reference efflux at 10 °C (F₁₀) of 2.6 μmol m⁻² s⁻¹ and the Q₁₀ of 3.7. No evidence of displacement of CO₂-rich soil air with rain was observed.Effluxes calculated from soil CO₂ concentration gradients near the surface closely agreed with the measured effluxes. Calculations indicated that more than 75% of the soil CO₂ efflux originated in the top 20 cm soil. Calculated CO₂ production varied with soil temperature, soil water content and season, and when scaled to 10 °C also showed some diurnal variation. Soil CO₂ efflux and concentrations as well as soil temperature at the 5-cm depth varied in phase. Changes in CO₂ storage in the 0–50 cm soil layer were an order of magnitude smaller than measured effluxes. Soil CO₂ efflux was proportional to CO₂ concentration at the 50-cm depth with the slope determined by soil water content, which was consistent with a simple steady-state analytical model of diffusive transport of CO₂ in the soil. The latter proved successful in calculating effluxes during 2004.     

Determinants of annual fluxes of CO2 and N2O in long-term no-tillage and conventional tillage systems in northern France

The greenhouse gases CO₂ and N₂O emissions were quantified in a long-term experiment in northern France, in which no-till (NT) and conventional tillage (CT) had been differentiated during 32 years in plots under a maize–wheat rotation. Continuous CO₂ and periodical N₂O soil emission measurements were performed during two periods: under maize cultivation (April 2003–July 2003) and during the fallow period after wheat harvest (August 2003–March 2004). In order to document the dynamics and importance of these emissions, soil organic C and mineral N, residue decomposition, soil potential for CO₂ emission and climatic data were measured. CO₂ emissions were significantly larger in NT on 53% and in CT on 6% of the days. From April to July 2003 and from November 2003 to March 2004, the cumulated CO₂ emissions did not differ significantly between CT and NT. However, the cumulated CO₂ emissions from August to November 2003 were considerably larger for NT than for CT. Over the entire 331 days of measurement, CT and NT emitted 3160 ± 269 and 4064 ± 138 kg CO₂-C ha⁻¹, respectively. The differences in CO₂ emissions in the two tillage systems resulted from the soil climatic conditions and the amounts and location of crop residues and SOM. A large proportion of the CO₂ emissions in NT over the entire measurement period was probably due to the decomposition of old weathered residues. NT tended to emit more N₂O than CT over the entire measurement period. However differences were statistically significant in only half of the cases due to important variability. N₂O emissions were generally less than 5 g N ha⁻¹ day⁻¹, except for a few dates where emission increased up to 21 g N ha⁻¹ day⁻¹. These N₂O fluxes represented 0.80 ± 0.15 and 1.32 ± 0.52 kg N₂O-N ha⁻¹ year⁻¹ for CT and NT, respectively. Depending on the periods, a large part of the N₂O emissions occurred was probably induced by nitrification, since soil conditions were not favorable for denitrification. Finally, for the period of measurement after 32 years of tillage treatments, the NT system emitted more greenhouses gases (CO₂ and N₂O) to the atmosphere on an annual basis than the CT system.     

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.     

N2O and NO fluxes between a Norway spruce forest soil and atmosphere as affected by prolonged summer drought

Global change scenarios predict an increasing frequency and duration of summer drought periods in Central Europe especially for higher elevation areas. Our current knowledge about the effects of soil drought on nitrogen trace gas fluxes from temperate forest soils is scarce. In this study, the effects of experimentally induced drought on soil N₂O and NO emissions were investigated in a mature Norway spruce forest in the Fichtelgebirge (northeastern Bavaria, Germany) in two consecutive years. Drought was induced by roof constructions over a period of 46 days. The experiment was run in three replicates and three non-manipulated plots served as controls. Additionally to the N₂O and NO flux measurements in weekly to monthly intervals, soil gas samples from six different soil depths were analysed in time series for N₂O concentration as well as isotope abundances to investigate N₂O dynamics within the soil. N₂O fluxes from soil to the atmosphere at the experimental plots decreased gradually during the drought period from 0.2 to −0.0 μmol m⁻² h⁻¹, respectively, and mean cumulative N₂O emissions from the manipulated plots were reduced by 43% during experimental drought compared to the controls in 2007. N₂O concentration as well as isotope abundance analysis along the soil profiles revealed that a major part of the soil acted as a net sink for N₂O, even during drought. This N₂O sink, together with diminished N₂O production in the organic layers, resulted in successively decreased N₂O fluxes during drought, and may even turn this forest soil into a net sink of atmospheric N₂O as observed in the first year of the experiment. Enhanced N₂O fluxes observed after rewetting up to 0.1 μmol m⁻² h⁻¹ were not able to compensate for the preceding drought effect. During the experiment in 2006, with soil matric potentials in 20 cm depth down to −630 hPa, cumulative NO emissions from the throughfall exclusion plots were reduced by 69% compared to the controls, whereas cumulative NO emissions from the experimental plots in 2007, with minimum soil matric potentials of −210 hPa, were 180% of those of the controls. Following wetting, the soil of the throughfall exclusion plots showed significantly larger NO fluxes compared to the controls (up to 9 μmol m⁻² h⁻¹ versus 2 μmol m⁻² h⁻¹). These fluxes were responsible for 44% of the total emission of NO throughout the whole course of the experiment. NO emissions from this forest soil usually exceeded N₂O emissions by one order of magnitude or more except during wintertime.     

Drying-rewetting events reduce C and N losses from a Norway spruce forest floor

Periods of prolonged summer drought are likely to be expected for this century, with possibly strong effects on carbon (C) and nitrogen (N) mineralization in soils. Drought generally reduces mineralization rates, but the possibility of excess mineralization pulses during rewetting raises the question about the net effect of drying-rewetting events. In this experiment, we measured C and N mineralization in undisturbed soil columns that were either kept under continuously moist conditions (control) or that were subjected to drying-rewetting. We had three treatments (D1-D3) with different drying intensity (increasing from D1 to D3) but uniform rewetting intensity (4 mm d⁻¹). Soil columns were taken from a Norway spruce forest in Bavaria, Germany. The CO₂ fluxes from control and treatment groups were identical before drying. Over the 80 d drought period, total CO₂ emissions from D1, D2, and D3 were only 72, 52 and 43% of that from the control, respectively. Rewetting resulted in a fast increase of CO₂ fluxes to approx. the same level as in the control. Rewetting could not restore soil moisture of the dry soil to the level of the control, presumably because of preferential flow and water repellency of soil organic matter. No significant excess C mineralization during the 40 d rewetting period was observed. Adding up total CO₂ fluxes during drought and rewetting period, the treatments D1, D2, and D3 emitted only 88, 71 and 67% of the CO₂ emitted by the control. Measurements of dissolved organic carbon (DOC) did only show minor differences between control and treatment columns, indicating that no significant accumulation of DOC took place during the drought period. Radiocarbon signature of emitted CO₂ indicated that C mineralization was reduced with decreasing water availability and no new substrate became bioavailable. Net N mineralization over the course of the whole experiment was reduced by drought to 77, 65 or 52% of the control. Net nitrification was virtually zero during drought whereas net ammonification continued at reduced levels. In summary, we found that drying-rewetting generally reduced C and N mineralization in this soil and that the total reduction increased with drought intensity.     

Microbial processes and the site of N2O production in a temperate grassland soil

To understand nitrous oxide (N₂O) emissions from terrestrial ecosystems it is necessary to understand the processes leading to N₂O production. Here, for the first time, results are presented which identify in situ the processes of N₂O production in a temperate grassland soil. A small portion of the nitrogen (N) applied in the summer to the grassland soil was rapidly transported below the main rooting zone (>20 cm) and resulted in large N₂O productions at depths of 20-50 cm. Preferential pathways must have been responsible for this movement because the soil conditions were not conducive to leaching by piston flow. The N₂O was entirely produced by nitrate (NO₃⁻) reduction which was surprising because the bulk soil was aerobic. Therefore, reduction processes can operate during times of the year when it is least expected and cause large N₂O concentrations deep in the soil profile.     

Compaction influences N2O and N2 emissions from 15N-labeled synthetic urine in wet soils during successive saturation/drainage cycles

Nitrous oxide emitted from urine patches is a key source of agricultural greenhouse gas emissions. A better understanding of the complex soil environmental and biochemical regulation of urine-N transformations in wet soils is needed to predict N₂O emissions from grazing and also to develop targeted mitigation technologies. Soil aeration, gas diffusion and drainage are key factors regulating N transformations and are affected by compaction during grazing. To understand how soil compaction from animal treading influences N transformations of urine in wet soils, we applied pressures of 0, 220 and 400 kPa to repacked soil cores, followed by ¹⁵N-labeled synthetic urine, and then subjected the cores to three successive saturation–drainage cycles on tension tables from 0 to 10 kPa.Compaction had a relatively small effect on soil bulk density (increasing from 0.81 to 0.88 Mg m⁻³), but strongly affected the pore size distribution. Compaction reduced both total soil porosity and macroporosity. It also affected the pore size distribution, principally by decreasing the proportion of 30–60 μm and 60–100 μm pores and increasing the proportion of micropores (<30 μm).Rates of urine-N transformations, emissions of N₂ and N₂O, and the N₂O to N₂ ratio were affected by the saturation/drainage cycles and degree of compaction. During the first saturation–drainage cycle, production of both N₂O and N₂ was low (<0.4 mg N m⁻² h⁻¹), probably because of anaerobic conditions inhibiting nitrification. In the second saturation/drainage cycle, the predominant product was N₂ at all compaction rates. By the third cycle, with increasing availability of mineral-N substrates, N₂O was the dominant product in the uncompacted (max = 4.70 mg N m⁻² h⁻¹) and 220 kPa compacted soils (max = 7.65 mg N m⁻² h⁻¹) with lower amounts of N₂ produced, while N₂ was produced in similar quantities to N₂O (max = 3.11 mg N m⁻² h⁻¹) in the 400 kPa compacted soil. Reduced macroporosity in the most compacted soil contributed to more sustained N₂ and N₂O production as the soils drained. In addition, compaction affected the rate of change of soil pH and DOC, both of which affected the N₂O to N₂ ratio.Denitrification during drainage and re-saturation may make a large contribution to soil N₂O emissions. Improving soil drainage and adopting grazing management practices that avoid soil compaction while increasing macroporosity will reduce total N₂O and N₂ emissions.     

Effects of land-use type and nitrogen addition on nitrous oxide and carbon dioxide production potentials in Japanese Andosols

Land-use type and nitrogen (N) addition strongly affect nitrous oxide (N₂O) and carbon dioxide (CO₂) production, but the impacts of their interaction and the controlling factors remain unclear. The aim of this study was to evaluate the effect of both factors simultaneously on N₂O and CO₂ production and associated soil chemical and biological properties. Surface soils (0–10 cm) from three adjacent lands (apple orchard, grassland and deciduous forest) in central Japan were selected and incubated aerobically for 12 weeks with addition of 0, 30 or 150 kg N ha^–1 yr^–1. Land-use type had a significant (p < 0.001) impact on the cumulative N₂O and CO₂ production. Soils from the apple orchard had higher N₂O and CO₂ production potentials than those from the grassland and forest soils. Soil net N mineralization rate had a positive correlation with both soil N₂O and CO₂ production rates. Furthermore, the N₂O production rate was positively correlated with the CO₂ production rate. In the soils with no N addition, the dominant soil properties influencing N₂O production were found to be the ammonium-N content and the ratio of soil microbial biomass carbon to nitrogen (MBC/MBN), while those for CO₂ production were the content of nitrate-N and soluble organic carbon. N₂O production increased with the increase in added N doses for the three land-use types and depended on the status of the initial soil available N. The effect of N addition on CO₂ production varied with land use type; with the increase of N addition doses, it decreased for the apple orchard and forest soils but increased for the grassland soils. This difference might be due to the differences in microbial flora as indicated by the MBC/MBN ratio. Soil N mineralization was the major process controlling N₂O and CO₂ production in the examined soils under aerobic incubation conditions.     

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.