Carbon sequestration in agricultural soils in the Cerrado region of the Brazilian Amazon

The introduction of crop management practices after conversion of Amazon Cerrado into cropland influences soil C stocks and has direct and indirect consequences on greenhouse gases (GHG) emissions. The aim of this study was to quantify soil C sequestration, through the evaluation of the changes in C stocks, as well as the GHG fluxes (N₂O and CH₄) during the process of conversion of Cerrado into agricultural land in the southwestern Amazon region, comparing no-tillage (NT) and conventional tillage (CT) systems. We collected samples from soils and made gas flux measurements in July 2004 (the dry season) and in January 2005 (the wet season) at six areas: Cerrado, CT cultivated with rice for 1 year (1CT) and 2 years (2CT), and NT cultivated with soybean for 1 year (1NT), 2 years (2NT) and 3 years (3NT), in each case after a 2-year period of rice under CT. Soil samples were analyzed in both seasons for total organic C and bulk density. The soil C stocks, corrected for a mass of soil equivalent to the 0–30-cm layer under Cerrado, indicated that soils under NT had generally higher C storage compared to native Cerrado and CT soils. The annual C accumulation rate in the conversion of rice under CT into soybean under NT was 0.38 Mg ha⁻¹ year⁻¹. Although CO₂ emissions were not used in the C sequestration estimates to avoid double counting, we did include the fluxes of this gas in our discussion. In the wet season, CO₂ emissions were twice as high as in the dry season and the highest N₂O emissions occurred under the NT system. There were no CH₄ emissions to the atmosphere (negative fluxes) and there were no significant seasonal variations. When N₂O and CH₄ emissions in C-equivalent were subtracted (assuming that the measurements made on 4 days were representative of the whole year), the soil C sequestration rate of the conversion of rice under CT into soybean under NT was 0.23 Mg ha⁻¹ year⁻¹. Although there were positive soil C sequestration rates, our results do not present data regarding the full C balance in soil management changes in the Amazon Cerrado.     

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.     

Seasonal variations of nitrous oxide emission in relation to nitrogen fertilization and energy crop types in sandy soil

Nitrous oxide (N₂O) is a greenhouse gas and agricultural soils are major sources of atmospheric N₂O. Its emissions from soils make up the largest part in the global N₂O budget. Research was carried out at the experimental fields of the Leibniz-Institute of Agricultural Engineering Potsdam-Bornim (ATB). Different types (mineral and wood ash) and levels (0, 75 and 150 kg N ha⁻¹) of fertilization were applied to annual (rape, rye, triticale and hemp) and perennial (poplar and willow) plants every year. N₂O flux measurements were performed 4 times a week by means of gas flux chambers and an automated gas chromatograph between 2003 and 2005. Soil samples were also taken close to the corresponding measuring rings. Soil nitrate and ammonium were measured in soil extracts.N₂O emissions had a peak after N fertilization in spring, after plant harvest in summer and during the freezing–thawing periods in winter. Both fertilization and plant types significantly altered N₂O emission. The maximum N₂O emission rate detected was 1081 μg N₂O m⁻² h⁻¹ in 2004. The mean annual N₂O emissions from the annual plants were more than twofold greater than those of perennial plants (4.3 kg ha⁻¹ vs. 1.9 kg ha⁻¹). During January, N₂O fluxes considerably increased in all treatments due to freezing–thawing cycles. Fertilization together with annual cropping doubled the N₂O emissions compared to perennial crops indicating that N use efficiency was greater for perennial plants. Fertilizer-derived N₂O fluxes constituted about 32% (willow) to 67% (rape/rye) of total soil N₂O flux. Concurrent measurements of soil water content, NO₃ and NH₄ support the conclusion that nitrification is main source of N₂O loss from the study soils. The mean soil NO₃-N values of soils during the study for fertilized soils were 1.6 and 0.9 mg NO₃-N kg⁻¹ for 150 and 75 kg N ha⁻¹ fertilization, respectively. This value reduced to 0.5 mg NO₃-N kg⁻¹ for non-fertilized soils.     

林分类型和氮添加对亚热带森林土壤氧化亚氮排放的影响

为揭示亚热带森林土壤N₂O排放对林分类型和氮添加的响应特征,选取位于福建省三明市的中亚热带米槠次生林、杉木人工林和马尾松人工林土壤为研究对象,分别设置无氮添加(N0 mg/kg)、低氮添加(N10 mg/kg)、中氮添加(N25 mg/kg)和高氮添加(N50 mg/kg)4个氮添加水平,进行微宇宙培养试验,测定土壤N₂O排放。结果表明：与无氮添加处理相比,氮添加整体上降低3种林分土壤pH,增加土壤NH₄⁺-N和NO₃^--N含量。无氮添加处理中杉木人工林和马尾松人工林土壤N₂O累积排放量分别为9.67和9.62 mg/kg,显著高于米槠次生林土壤N₂O累积排放量6.81 mg/kg。低氮添加处理中杉木人工林和马尾松人工林土壤N₂O累积排放量显著高于米槠次生林。但在中氮和高氮添加处理中,3种林分土壤N₂O累积排放量均无显著性差异。不同氮添加处理均促进3种林分土壤N     

The effect of mixing organic biological waste materials and high-N crop residues on the short-time N2O emission from horticultural soil in model experiments

Manipulating the N release from high-N crop residues by simultaneous mixing of these residues with organic biological waste (OBW) materials seems to be a possible method to reduce NO₃^– leaching. The aim of this study was to examine whether the incorporation of OBW materials together with a high-N crop residue (celery) had also an effect on N₂O emission from horticultural soil under short-term and optimised laboratory conditions. A sandy loam soil and celery residues were mixed with different OBW materials and brought into PVC tubes at 80% water-filled pore space and 15°C. Every 2.5 h, a gas sample was taken and analysed by gas chromatography for its N₂O concentration. The soil amended with only celery residues had a cumulative N₂O emission of 9.6 mg N kg^–1 soil in 50 h. When the celery residues were mixed with an OBW material, the N₂O emission was each time lower than the emission from the celery-only treatment (between 3.8 and 5.9 mg N kg^–1 soil during maximum 77 h), except with paper sludge (17.2 mg N kg^–1 soil in 100 h). The higher N₂O emission from the paper sludge treatment was probably due to its unusually low C:N ratio. Straw, green waste compost 1 (GWC1) and 2 (GWC2), saw dust, and tannic acid reduced the N₂O emission of the celery treatment by 40 to 60%. Although the N₂O reduction potential can be expected to be lower and with differing dynamics under field conditions, this study indicates that apart from reducing NO₃^– leaching, OBW application may at the same time reduce N₂O emissions after incorporation of high-N crop residues.     

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.     

Variability of CO2 and N2O emissions during freeze‐thaw cycles: results of model experiments on undisturbed forest‐soil cores

The amounts of N₂O released in periods of alternate freezing and thawing depend on site and freezing conditions, and contribute considerably to the annual N₂O emissions. However, quantitative information on the N₂O emission level of forest soils in freeze‐thaw cycles is scarce, especially with regard to the direct and indirect effect of tree species and the duration of freezing. Our objectives were (i) to quantify the CO₂ and N₂O emissions of three soils under beech which differed in their texture, C and N contents, and humus types in freeze‐thaw cycles, and (ii) to study the effects of the tree species (beech (Fagus sylvatica L.) and spruce (Picea abies (L.) Karst.)) for silty soils from two adjacent sites and the duration of freezing (three and eleven days) on the emissions. Soils were adjusted to a matric potential of –0.5 kPa, and emissions were measured in 3‐hr intervals for 33 days. CO₂ emissions of all soils were similar in the two freeze‐thaw cycles, and followed the temperature course. In contrast, the N₂O emissions during thawing differed considerably. Large N₂O emissions were found on the loamy soil under beech (Loam‐beech) with a maximum N₂O emission of 1200 μg N m^–2 h^–1 and a cumulative emission of 0.15 g N m^–2 in the two thawing periods. However, the sandy soil under beech (Sand‐beech) emitted only 1 mg N₂O‐N m^–2 in the two thawing periods probably because of a low water‐filled pore space of 44 %. The N₂O emissions of the silty soil under beech (Silt‐beech) were small (9 mg N m^–2 in the two thawing periods) with a maximum emission of 150 μg N m^–2 h^–1 while insignificant N₂O emissions were found on the silty soil under spruce (0.2 mg N m^–2 in the two thawing periods). The cumulative N₂O emissions of the short freeze‐thaw cycles were 17 % (Sand‐beech) or 22 % (Loam‐beech, Silt‐beech) less than those of the long freeze‐thaw cycles, but the differences between the emissions of the two periods were not significant (P ≤ 0.05). The results of the study show that the amounts of N₂O emitted in freeze‐thaw cycles vary markedly among different forest soils and that the tree species influence the N₂O thawing emissions in forests considerably due to direct and indirect impacts on soil physical and chemical properties, soil structure, and properties of the humus layer.     

Spatial variability of N2O emissions and soil parameters of an arable silt loam – a field study

 The spatial in situ variability of soil N₂O emissions (measured by micro-chambers, radius 0.033 m), N₂O content, water content, NO₃ ^–, NH₄ ⁺, inorganic carbon and organic carbon concentrations was investigated on a silt loam by means of geostatistical methods and nonparametric statistics. The sampling grid consisted of different spacings between sampling points which ranged from 0.1 m to 50 m. There were no significant correlations between N₂O emissions and soil parameters (P>0.1) when all the sampling points were considered. In the centre of the grid a "hot area" was localized with significantly higher N₂O emissions, and NO₃ ^– and NH₄ ⁺ concentrations (P≤0.05). Within this hot area the N₂O soil content significantly correlated with N₂O emissions (P≤0.05). When semiovariograms were computed without data of the hot area samples, N₂O emissions showed a weak spatial correlation (range: 4.3 m). The calculations including all data led to pure nugget effects for all parameters except for soil water content (range >40 m) and N₂O soil content (range 16.4 m). Received: 19 December 1997     

Dinitrogen emissions and the N2:N2O emission ratio of a Rendzic Leptosol as influenced by pH and forest thinning

Reduction of nitrous oxide (N₂O) to dinitrogen (N₂) by denitrification in soils is of outstanding ecological significance since it is the prevailing natural process converting reactive nitrogen back into inert molecular dinitrogen. Furthermore, the extent to which N₂O is reduced to N₂ via denitrification is a major regulating factor affecting the magnitude of N₂O emission from soils. However, due to methodological problems in the past, extremely little information is available on N₂ emission and the N₂:N₂O emission ratio for soils of terrestrial ecosystems. In this study, we simultaneously determined N₂ and N₂O emissions from intact soil cores taken from a mountainous beech forest ecosystem. The soil cores were taken from plots with distinct differences in microclimate (warm-dry versus cool-moist) and silvicultural treatment (untreated control versus heavy thinning). Due to different microclimates, the plots showed pronounced differences in pH values (range: 6.3–7.3). N₂O emission from the soil cores was generally very low (2.0 ± 0.5–6.3 ± 3.8 μg N m⁻² h⁻¹ at the warm-dry site and 7.1 ± 3.1–57.4 ± 28.5 μg N m⁻² h⁻¹ at the cool-moist site), thus confirming results from field measurements. However, N₂ emission exceeded N₂O emission by a factor of 21 ± 6–220 ± 122 at the investigated plots. This illustrates that the dominant end product of denitrification at our plots and under the given environmental conditions is N₂ rather than N₂O. N₂ emission showed a huge variability (range: 161 ± 64–1070 ± 499 μg N m⁻² h⁻¹), so that potential effects of microclimate or silvicultural treatment on N₂ emission could not be identified with certainty. However, there was a significant effect of microclimate on the magnitude of N₂O emission as well as on the mean N₂:N₂O emission ratio. N₂:N₂O emission ratios were higher and N₂O emissions were lower for soil cores taken from the plots with warm-dry microclimate as compared to soil cores taken from the cool-moist microclimate plots. We hypothesize that the increase in the N₂:N₂O emission ratio at the warm-dry site was due to higher N₂O reductase activity provoked by the higher soil pH value of this site. Overall, the results of this study show that the N₂:N₂O emission ratio is crucial for understanding the regulation of N₂O fluxes of the investigated soil and that reliable estimates of N₂ emissions are an indispensable prerequisite for accurately calculating total N gas budgets for the investigated ecosystem and very likely for many other terrestrial upland ecosystems as well.     

Ranking factors affecting emissions of GHG from incubated agricultural soils

Agriculture significantly contributes to global greenhouse gas (GHG) emissions and there is a need to develop effective mitigation strategies. The efficacy of methods to reduce GHG fluxes from agricultural soils can be affected by a range of interacting management and environmental factors. Uniquely, we used the Taguchi experimental design methodology to rank the relative importance of six factors known to affect the emission of GHG from soil: nitrate (NO₃^?) addition, carbon quality (labile and non‐labile C), soil temperature, water‐filled pore space (WFPS) and extent of soil compaction. Grassland soil was incubated in jars where selected factors, considered at two or three amounts within the experimental range, were combined in an orthogonal array to determine the importance and interactions between factors with a L₁₆ design, comprising 16 experimental units. Within this L₁₆ design, 216 combinations of the full factorial experimental design were represented. Headspace nitrous oxide (N₂O), methane (CH₄) and carbon dioxide (CO₂) concentrations were measured and used to calculate fluxes. Results found for the relative influence of factors (WFPS and NO₃^? addition were the main factors affecting N₂O fluxes, whilst glucose, NO₃^? and soil temperature were the main factors affecting CO₂ and CH₄ fluxes) were consistent with those already well documented. Interactions between factors were also studied and results showed that factors with little individual influence became more influential in combination. The proposed methodology offers new possibilities for GHG researchers to study interactions between influential factors and address the optimized sets of conditions to reduce GHG emissions in agro‐ecosystems, while reducing the number of experimental units required compared with conventional experimental procedures that adjust one variable at a time.     

The dynamics of N2O near the groundwater table and the transfer of N2O into the unsaturated zone: A case study from a sandy aquifer in Germany

The research area was the Fuhrberger Feld aquifer (FFA) in northern Germany. It is situated about 30km northeast of the city of Hannover and covers about 300km². Six multilevel sampling wells along a representative strip under predominantly arable land along a groundwater flow-line were sampled from the groundwater table down to a depth of 10m below the soil surface. We measured N₂O, CO₂, NO₃⁻, SO₄²⁻, DOC, pH, redox potentials and O₂ concentrations.N₂O accumulated at four out of six wells close to the groundwater table. About 20% of N₂O that occurred between the groundwater table and 7–8m below it resided in the top 0.4m. An exchange zone for N₂O at the interface between the saturated and the unsaturated zone extended 0.55 ± 0.22m below the groundwater table and acted as a source and sink for N₂O. N₂O below the exchange zone cannot be transferred from the groundwater to the atmosphere. The upward fluxes from the exchange zone into the unsaturated zone at the six wells ranged between 0.0009 and 0.3kg N₂O ha^{− 1} year^{− 1}. The yearly downward fluxes into the exchange zones had about the same order of magnitude as the upward fluxes. The upward and downward fluxes of N₂O at the (fluctuating) water table did cancel out each other, but this does not yet imply, that the N₂O fluxes at the soil surface also cancel out each other.N₂O–N:NO₃–N ratios were highly variable ranging from 0.0002 to 0.0417.A multiple regression for the monthly N₂O amounts in the exchange zone could explain 66% of the yearly variation. The significant variables were NO₃⁻, CO₂, pH, and O₂. Therefore, a combination of the land use (NO₃⁻), the geochemical boundary conditions (pH) and the type of denitrification reaction (O₂ and CO₂ indicate the importance of a heterotrophic denitrification process) governed the N₂O dynamics in the surface groundwater of the FFA and its transfer into the unsaturated zone.     

Effect of soil water status and mulching on N<Subscript>2</Subscript>O and CH<Subscript>4</Subscript> emission from lowland rice field in China

Cultivation of rice in unsaturated soils covered with mulch is receiving more attention in China because of increasingly serious water shortage; however, greenhouse gas emission from this cultivation system is still poorly understood. A field experiment was conducted in 2001 to compare nitrous oxide (N₂O) and methane (CH₄) emission from rice cultivated in unsaturated soil covered with plastic or straw mulch and the traditional waterlogged production system. Trace gas fluxes from the soil were measured weekly throughout the entire growth period using a closed chamber method. Nitrous oxide emissions from unsaturated rice fields were large and varied considerably during the rice season. They were significantly affected by N fertilizer application rate. In contrast, N₂O emission from the waterlogged system was very low with a maximum of 0.28 mg N₂O m^–2 h^–1. However, CH₄ emission from the waterlogged system was significantly higher than from the unsaturated system, with a maximum emission rate of 5.01 mg CH₄ m^–2 h^–1. Our results suggested that unsaturated rice cultivation with straw mulch reduce greenhouse gas emissions.     

Nitrous oxide emissions from agricultural soils at low temperatures: a laboratory microcosm study

We studied in laboratory microcosms (intact soil cores) N₂O and CO₂ emissions from four different agricultural soil types (organic soil, clay, silt and loam) at low temperatures with or without freezing-thawing events. When the temperature of the frozen soil cores was increased stepwise from −8 °C the N₂O emissions began to increase at −0.5 °C, and peaked at −0.1 °C in the organic, clay and silt soils, and at +1.6 °C in the loam soils. However, a stepwise decrease in soil temperature from +15 °C also induced an increase in the N₂O emissions close to the 0 °C. These emissions peaked between −0.4 and +2.5 °C depending on the soil type and water content. However, the emission maxima were from 2 to 14.3% of those encountered in the experiments where frozen soils were thawed. Our results show that in addition to the well-documented thawing peak, soils also can have a maximum in their N₂O emission near 0 °C when soil temperature decrease. These emissions, however, are less than those emitted from thawing soils. The correlations between the N₂O and CO₂ emissions were weak. Our results suggest that N₂O is produced in soils down to a temperature of −6 °C.     

Temporal and spatial patterns of denitrification enzyme activity and nitrous oxide fluxes in three adjacent vegetated riparian buffer zones

The aim of this study was to investigate temporal and spatial patterns of denitrification enzyme activity (DEA) and nitrous oxide (N₂O) fluxes in three adjacent riparian sites (mixed vegetation, forest and grass). The highest DEA was found in the surface (0–30 cm) soil and varied between 0.7±0.1 mg N kg^–1 day^–1 at 5°C and 5.9±0.4 mg N kg^–1 day^–1 at 15°C. There was no significant difference (P >0.05) between the DEA in the uppermost (0–30 cm and 60–90 cm) soil depths under different vegetation covers. In the two deepest (120–150 cm and 180–210 cm) soil depths the DEA varied between 0.0±0.0 mg N kg^–1 day^–1 at 5°C and 4.4±0.9 mg N kg^–1 day^–1 at 15°C and was clearly associated with the accumulation of buried organic carbon (OC). Two threshold values of OC were observed before DEA started to increase significantly, namely 5 and 25 g OC kg^–1 soil at 10–15°C and 5°C, respectively. In the three riparian sites N₂O fluxes varied between a net N₂O uptake of –0.6±0.4 mg N₂O-N m^–2 day^–1 and a net N₂O emission of 2.5±0.3 mg N₂O-N m^–2 day^–1. The observed N₂O emission did not lead to an important pollution swapping (from water pollution to greenhouse gas emission). Especially in the mixed vegetation and forest riparian site highest N₂O fluxes were observed upslope of the riparian site. The N₂O fluxes showed no clear temporal trend.     

Contributions of nitrification and denitrification to N2O emissions from soils at different water-filled pore space

A combination of stable isotope and acetylene (0.01% v/v) inhibition techniques were used for the first time to determine N₂O production during denitrification, autotrophic nitrification and heterotrophic nitrification in a fertilised (200 kg N ha^–1) silt loam soil at contrasting (20–70%) water-filled pore space (WFPS). ¹⁵N-N₂O emissions from ¹⁴NH₄¹⁵NO₃ replicates were attributed to denitrification and ¹⁵N-N₂O from ¹⁵NH₄¹⁵NO₃ minus that from ¹⁴NH₄¹⁵NO₃ replicates was attributed to nitrification and heterotrophic nitrification in the presence of acetylene, as there was no dissimilatory nitrate reduction to ammonium or immobilisation and remineralisation of ¹⁵N-NO₃^–. All of the N₂O emitted at 70% WFPS (31.6 mg N₂O-N m^–2 over 24 days; 1.12 g N₂O-N g dry soil^–1; 0.16% of N applied) was produced during denitrification, but at 35–60% WFPS nitrification was the main process producing N₂O, accounting for 81% of ¹⁵N-N₂O emitted at 60% WFPS, and 7.9 g ¹⁵N-N₂O m^–2 (0.28 ng ¹⁵N-N₂O g dry soil^–1) was estimated to be emitted over 7 days during heterotrophic nitrification in the 50% WFPS treatment and accounted for 20% of ¹⁵N-N₂O from this treatment. Denitrification was the predominant N₂O-producing process at 20% WFPS (2.6 g ¹⁵N-N₂O m^–2 over 7 days; 0.09 ng ¹⁵N-N₂O g dry soil^–1; 85% of ¹⁵N-N₂O from this treatment) and may have been due to the occurrence of aerobic denitrification at this WFPS. Our results demonstrate the usefulness of a combined stable isotope and acetylene approach to quantify N₂O emissions from different processes and to show that several processes may contribute to N₂O emission from agricultural soils depending on soil WFPS.     

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.     

Nitrous oxide emission from frozen grassland soil and during thawing periods

Nitrous oxide (N₂O) was emitted during a frost period from an old grassland as well as during thawing. Soil incubations at various times throughout the freezing period showed that highest emission rates were emitted around 0 °C, and the magnitude of the emission peak increased with the length of the freezing period. Highest N₂O emissions during freezing and thawing were measured from soil previously treated with nitrate (NO₃^‐). The emitted N₂O was produced via reduction of NO₃^‐. The steady drop in N₂O emission at soil temperatures higher than 2 °C coincided with large dinitrogen (N₂) emissions which most likely reflected the increasing enzymatic activity of N₂O reductase with increasing temperatures. Measurements of mineral N concentrations showed that NO₃^‐ and NH₄⁺, which were shortly after fertilizer application immobilized into the microbial biomass, became partly available again through the freezing effect and caused large N₂O emissions in winter. This study provided evidence that N₂O emissions during freezing and thawing in the winter are due to biological rather than chemical activity in soil.     

The effect of reduced tillage on nitrous oxide emissions of silt loam soils

The effect of reduced tillage (RT) on nitrous oxide (N₂O) emissions of soils from fields with root crops under a temperate climate was studied. Three silt loam fields under RT agriculture were compared with their respective conventional tillage (CT) field with comparable crop rotation and manure application. Undisturbed soil samples taken in September 2005 and February 2006 were incubated under laboratory conditions for 10 days. The N₂O emission of soils taken in September 2005 varied from 50 to 1,095 μg N kg⁻¹ dry soil. The N₂O emissions of soils from the RT fields taken in September 2005 were statistically (P < 0.05) higher or comparable than the N₂O emissions from their respective CT soil. The N₂O emission of soils taken in February 2006 varied from 0 to 233 μg N kg⁻¹ dry soil. The N₂O emissions of soils from the RT fields taken in February 2006 tended to be higher than the N₂O emissions from their respective CT soil. A positive and significant Pearson correlation of the N₂O–N emissions with nitrate nitrogen (NO₃ ⁻–N) content in the soil was found (P < 0.01). Leaving the straw on the field, a typical feature of RT, decreased NO₃ ⁻–N content of the soil and reduced N₂O emissions from RT soils.     

N2O emissions from different cropping systems and from aerated,nitrifying and denitrifying tanks of a municipal waste water treatment plant

Nitrous oxide emissions, nitrate, water-soluble carbon and biological O₂ demand (BOD₅) were quantified in different cropping systems fertilized with varying amounts of nitrogen (clayey loam, October 1991 to May 1992), in an aerated tank (March 1993 to March 1994), and in the nitrification-denitrification unit (March to July 1994) of a municipal waste water treatment plant. In addition, the N₂O present in the soil body at different depths was determined (February to July 1994). N₂O was emitted by all cropping systems (mean releases 0.13–0.35 mg N₂O m^-2 h^-1), and all the units of the domestic waste water treatment plant (aerated tank 0–6.2 mg N₂O m^-2 h^-1, nitrification tank 0–204,3 mg N₂O m^-2, h^-1, denitrifying unit 0–2.2 mg N₂O m^-2 h^-1). During the N₂O-sampling periods estimated amounts of 0.9, 1.5, 2.4 and 1.4 kg N₂O–N ha^-1, respectively, were released by the cropping systems. The aerated, nitrifying and denitrifying tanks of the municipal waste water treatment plant released mean amounts of 9.1, 71.6 and 1.8 g N₂O–N m^-2, respectively, during the sampling periods.The N₂O emission were significantly positively correlated with nitrate concentrations in the field plots which received no N fertilizer and with the nitrogen content of the aerated sludge tank that received almost exclusively N in the form of NH ₄ ⁺ . Available carbon, in contrast, was significantly negatively correlated with the N₂O emitted in the soil fertilized with 80 kg N ha^-1 year. The significant negative correlation between the emitted N₂O and the carbon to nitrate ratio indicates that the lower the carbon to nitrate ratio the higher the amount of N₂O released. Increasing N₂O emissions seem to occur at electron donorto-acceptor ratios (C_H2_O or BOD₅-to-nitrate ratios) below 50 in the cropping systems and below 1200–1400 in the waste water treatment plant. The trapped N₂O in the soil body down to a depth of 90 cm demonstrates that agricultural production systems seem to contain a considerable pool of N₂O which may be reduced to N₂ on its way to the atmosphere, which may be transported to other environments or which may be released at sometime in the future.Dedicated to Professor J.C.G. Ottow on the occasion of his 60th birthday     

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.