Two-year field study on the emission of N2O from coarse and middle-textured Belgian soils with different land use

In the following study N₂O emissions from 3 different grasslands and from 3 different arable lands, representing major agriculture areas with different soil textures and normal agricultural practices in Belgium, have been monitored for 1 to 2 years. One undisturbed soil under deciduous forest was also included in the study. Nitrous oxide emission was measured directly in the field from vented closed chambers through photo-acoustic infrared detection. Annual N₂O emissions from the arable lands ranged from 0.3 to 1.5 kg N ha⁻¹ y⁻¹ and represent 0.3 to 1.0% of the fertilizer N applied. Annual N₂O emissions from the intensively managed grasslands and an arable land sown with grass were significantly larger than those from the cropped arable lands. Emissions ranged from 14 to 32 kg N ha⁻¹ y⁻¹, representing fertilizer N losses between 3 and 11%. At the forest soil a net N₂O uptake of 1.3 kg N₂O-N ha⁻¹ was recorded over a 2-year period. It seems that the N₂O-N loss per unit of fertilizer N applied is larger for intensively managed and heavily fertilized (up to 500 kg N ha⁻¹) grasslands than for arable lands and is substantially larger than the 1.25% figure used for the global emission inventory. Comparison of the annual emission fluxes from the different soils also indicated that land use rather than soil properties influenced the N₂O emission. Our results also show once again the importance of year-round measurements for a correct estimate of N₂O losses from agricultural soils: 7 to 76% of the total annual N₂O was emitted during the winter period (October–February). Disregarding the emission during the off-season period can lead to serious underestimation of the actual annual N₂O flux. This revised version was published online in August 2006 with corrections to the Cover Date.     

Towards a Revised Coefficient for Estimating N2O Emissions from Legumes

The Intergovernmental Panel on Climate Change (IPCC) standard methodology to conduct national inventories of soil N₂O emissions is based on default (or Tier I) emission factors for various sources. The objective of our study was to summarize recent N₂O flux data from agricultural legume crops to assess the emission factor associated with rhizobial nitrogen fixation. Average N₂O emissions from legumes are 1.0 kg N ha⁻¹ for annual crops, 1.8 kg N ha⁻¹ for pure forage crops and 0.4 kg N ha⁻¹ for grass legume mixes. These values are only slightly greater than background emissions from agricultural crops and are much lower that those predicted using 1996 IPCC methodology. These field flux measurements and other process-level studies offer little support for the use of an emission factor for biological N fixation (BNF) by legume crops equal to that for fertiliser N. We conclude that much of the increase in soil N₂O emissions in legume crops may be attributable to the N release from root exudates during the growing season and from decomposition of crop residues after harvest, rather than from BNF per se. Consequently, we propose that the biological fixation process itself be removed from the IPCC N₂O inventory methodology, and that N₂O emissions induced by the growth of legume crops be estimated solely as a function of crop residue decomposition using an estimate of above- and below-ground residue inputs, modified as necessary to reflect recent findings on N allocation.     

The effect of biological oxygen demand of cattle slurry and soil moisture on nitrous oxide emissions

The application of animal manure slurries to soils may cause high short-term emissions of nitrous oxide (N₂O). We performed studies on N₂O emissions varying the contents of NH₄-N and microbial available organic carbon (measured as biological oxygen demand, BOD) of cattle slurry. Additionally the effect of slurry BOD on N₂O emissions at different soil water contents (35, 54, 71% water filled pore space, WFPS) was studied. Slurries from an anaerobic digestion plant (digested slurry, BOD: 1.2 g O₂ l⁻¹) or untreated slurry (BOD: 6.8 g O₂ l⁻¹) were applied at 30 m³ ha⁻¹ and incubated at 20°C. The higher the WFPS the more N₂O was emitted independent from the type of slurry applied. At low and medium soil water contents, the digested slurry induced significantly lower N₂O emissions than the untreated slurry. The N₂O emissions were directly correlated with the BOD content of the slurry (R ²=0.61, P≤0.001). We also compared the effect of NH₄-N concentration and BOD on emissions from the slurries at 54% WFPS. Again the BOD had a significant influence on N₂O emissions but a reduction of NH₄-N had no effect on the amount of N₂O emitted. The microbially available organic carbon seems to determine the amount of N₂O emitted shortly after slurry application. This revised version was published online in June 2006 with corrections to the Cover Date.     

Biologically Fixed N2 as a Source for N2O Production in a Grass–clover Mixture, Measured by 15N2

The contribution of biologically fixed dinitrogen (N₂) to the nitrous oxide (N₂O) production in grasslands is unknown. To assess the contribution of recently fixed N₂ as a source of N₂O and the transfer of fixed N from clover to companion grass, mixtures of white clover and perennial ryegrass were incubated for 14 days in a growth cabinet with a ¹⁵N₂-enriched atmosphere (0.4 atom% excess). Immediately after labelling, half of the grass–clover pots were sampled for N₂ fixation determination, whereas the remaining half were examined for emission of ¹⁵N labelled N₂O for another 8 days using a static chamber method. Biological N₂ fixation measured in grass–clover shoots and roots as well as in soil constituted 342, 38 and 67 mg N m⁻² d⁻¹ at 16, 26 and 36 weeks after emergence, respectively. The drop in N₂ fixation was most likely due to a severe aphid attack on the clover component. Transfer of recently fixed N from clover to companion grass was detected at 26 and 36 weeks after emergence and amounted to 0.7 ± 0.1 mg N m⁻² d⁻¹, which represented 1.7 ± 0.3% of the N accumulated in grass shoots during the labelling period. Total N₂O emission was 91, 416 and 259 μg N₂O–N m⁻² d⁻¹ at 16, 26 and 36 weeks after emergence, respectively. Only 3.2 ± 0.5 ppm of the recently fixed N₂ was emitted as N₂O on a daily basis, which accounted for 2.1 ± 0.5% of the total N₂O–N emission. Thus, recently fixed N released via easily degradable clover residues appears to be a minor source of N₂O. An erratum to this article is available at .     

Effect of crop-specific field management and N fertilization on N2O emissions from a fine-loamy soil

Agricultural soils are a major source of atmospheric N₂O. This study was conducted to determine the effect of different crop-specific field management and N fertilization rates on N₂O emissions from a fine-loamy Dystric Eutrochrept. Fluxes of N₂O were measured for two years at least once a week on plots cropped with potatoes (Solanum tuberosum) fertilized with 50 or 150 kg N ha⁻¹ a⁻¹, winterwheat (Triticum aestivum) fertilized with 90 or 180 kg N ha⁻¹ a⁻¹, corn (Zea mays) fertilized with 65 or 130 kg N ha⁻¹ a⁻¹, and on an unfertilized, set-aside soil planted with grass (mainly Lolium perenne and Festuca rubra). The mean N₂O emission rate from the differently managed plots was closely correlated to the mean soil nitrate content in the Ap horizon for the cropping period (April to October, r ² = 0.74), the winter period (November to March, r ² = 0.93, one outlier excluded), and the whole year (r ² = 0.81). N₂O emissions outside the cropping period accounted for up to 58% of the annual emissions and were strongly affected by frost-thaw cycles. There was only a slight relationship between the amount of fertilizer N applied and the annual N₂O emission (r ² = 0.20). The mean annual N₂O-N emission from the unfertilized set-aside soil was 0.29 kg ha⁻¹. The annual N₂O-N emission from the fertilized crops for the low and the recommended rates of N fertilization were 1.34 and 2.41 kg ha⁻¹ for corn, 2.70 and 3.64 kg ha⁻¹ for wheat, and 5.74 and 6.93 kg ha⁻¹ for potatoes. The high N₂O emissions from potato plots were due to (i) high N₂O losses from the interrow area during the cropping season and (ii) high soil nitrate contents after the potato harvest. The reduction of N fertilization (fertilizer was applied in spring and early summer) resulted in decreased N₂O emissions during the cropping period. However, the emissions during the winter were not affected by the rate of N fertilization. The results show that the crop-specific field management had a great influence on the annual N₂O emissions. It also affected the emissions per unit N fertilizer applied. The main reasons for this crop effect were crop-specific differences in soil nitrate and soil moisture content. This revised version was published online in June 2006 with corrections to the Cover Date.     

N2O emission from cropland in China

Based on the regionalization of uplands and paddy fields in China, the crop intensity in each region and the available field measurements, N₂O emission from cropland in China in 1995 was estimated to be 398 Gg N, in which, 310 Gg N was from uplands, accounting for 78% of the total. 88 Gg N–N₂O was emitted from paddy fields with 35 Gg N emitted during the rice growing season and 53 Gg N emitted during upland crop season. N₂O emission from upland and from paddy field during upland land crop season accounted for 91% of the total emission.     

The Effect of Future Climate Perturbations on N<Subscript>2</Subscript>O Emissions from a Fertilized Humid Grassland

N₂O emissions from a fertilized humid grassland near Cork, Ireland were continuously measured during 2003 using an eddy covariance system. For most of the year emissions were close to zero and 60% of the emissions occurred in eight major events of 2–20 days’ duration. Two hundred and seven kg ha⁻¹ of synthetic N and 130 kg ha⁻¹ organic N were applied over the year and the total measured annual N₂O emission was 11.6 kg N ha⁻¹. The flux data were used to test the prediction of N₂O emissions by the DNDC (DeNitrification – DeComposition) model. The model predicted total emissions of 15.4 kg N ha⁻¹, 32 % more than the observed emissions. On this basis the model was further used to simulate (a) background (non-anthropogenic) N₂O emissions and (b) the effect on N₂O emissions of future climate perturbations based on the Hadley Center model output of the IS92a scenario for Ireland. DNDC predicts 1.7 kg N ha⁻¹ year⁻¹ of background N₂O emissions, accounting for 15% of the observed emissions. Climate shifts will increase total annual modeled N₂O emissions from 15.4 kg N ha⁻¹ to 22.4 kg N ha⁻¹ if current levels of N applications are maintained, or to 21.2 kg N ha⁻¹ if synthetic N applications are reduced to 170 kg N ha⁻¹ to comply with recent EU water quality legislation. Thus the projected increase in N₂O emissions due to climate change is far larger than the decrease expected from reduced fertilizer applications.     

Urease and nitrification inhibitors to reduce emissions of CH4 and N2O in rice production

Strategies used to reduce emissions of N₂O and CH₄ in rice production normally include irrigation management and fertilization. To date, little information has been published on the measures that can simultaneously reduce both emissions. Effects of application of a urease inhibitor, hydroquinone (HQ), and a nitrification inhibitor, dicyandiamide (DCD) together with urea (U) on N₂O and CH₄ emission from rice growing were studied in pot experiments. These fertilization treatments were carried out in the presence and absence of wheat straw, applied to the soil surface. Without wheat straw addition, in all treatments with inhibitor(s) the emission of N₂O and CH₄ was significantly reduced, as compared with the treatment whereby only urea was applied (control). Especially for the U+HQ+DCD treatment, the total emission of N₂O and CH₄ was about 1/3 and 1/2 of that in the control, respectively. In the presence of wheat straw, the total N₂O emission from the U+HQ+DCD treatment was about 1/2 of that from the control. The total CH₄ emission was less influenced. Wheat straw addition, however, induced a substantial increase in emissions of N₂O and CH₄. Hence, simultaneous application of organic materials with a high C/N ratio and N-fertilizer (e.g. urea) is not a suitable method to reduce the N₂O and CH₄ emission. Application of HQ+DCD together with urea seemed to improve the rice growth and to reduce both emissions. The NO₃ ^–-N content of the rice plants and denitrification of (NO₃ ^–+NO₂ ^–)-N might contribute to the N₂O emission from flooded rice fields.     

Effects of type and amount of applied nitrogen fertilizer on nitrous oxide fluxes from intensively managed grassland

Five field experiments and one greenhouse experiment were carried out to assess the effects of nitrogen (N) fertilizer type and the amount of applied N fertilizer on nitrous oxide (N₂O) emission from grassland. During cold and dry conditions in early spring, emission of N₂O from both ammonium (NH ₄ ⁺ ) and nitrate (NO ₃ ^– ) containing fertilizers applied to a clay soil were relatively small, i.e. less than 0.1% of the N applied. Emission of N₂O and total denitrification losses from NO ₃ ^– containing fertilizers were large after application to a poorly drained sand soil during a wet spring. A total of 5–12% and 8–14% of the applied N was lost as N₂O and via denitrification, respectively. Emissions of N₂O and total denitrification losses from NH ₄ ⁺ fertilizers and cattle slurry were less than 2% of the N applied. Addition of the nitrification inhibitor dicyandiamide (DCD) reduced N₂O fluxes from ammonium sulphate (AS). However, the effect of DCD to reduce total N₂O emission from AS was much smaller than the effect of using NH ₄ ⁺ fertilizer instead of NO ₃ ^– fertilizer, during wet conditions. The greenhouse study showed that a high groundwater level favors production of N₂O from NO ₃ ^– fertilizers but not from NH ₄ ⁺ fertilizers. Inereasing calcium ammonium nitrate (CAN) application increased the emitted N₂O on grassland from 0.6% of the fertilizer application rate for a dressing of 50 kg N ha^–1 to 3.1% for a dressing of 300 kg N ha^–1. In another experiment, N₂O emission increased proportionally with increasing N rate. The results indicate that there is scope for reducing N₂O emission from grasslands by choosing the N fertilizer type depending on the soil moisture status. Avoiding excessive N application rates may also minimize N₂O emission from intensively managed grasslands.     

Mitigation potential of greenhouse gases under different scenarios of optimal synthetic nitrogen application rate for grain crops in China

Proper management of synthetic nitrogen (N) fertilizer can reduce direct N₂O emission from soil and indirect CO₂ emission from production and transportation of synthetic N. In the late 1990s, the average application rates of synthetic N were 212, 207 and 207 kg ha^?1, respectively, for rice, wheat, and maize in China’s croplands. But research suggests that the optimal synthetic N application rates for the main grain crops in China should be in the range of 110–150 kg ha^?1. Excessive application of synthetic N has undoubtedly resulted in massive emission of greenhouse gases. Therefore, optimizing N application rates for grain crops in China has a great potential for mitigating the emission of greenhouse gases. Nevertheless, this mitigation potential (MP) has not yet been well quantified. This study aimed at estimating the MP of N₂O and CO₂ emissions associated with synthetic N production and transportation in China based on the provincial level statistical data. Our research indicates that the total consumption of synthetic N on grain crops in China can be reduced by 5.0–8.4 Tg yr^?1 (28–47 % of the total consumption) if the synthetic N application rate is controlled at 110–150 kg ha^?1. The estimated total MP of greenhouse gases, including direct N₂O emission from croplands and indirect CO₂ emission from production and transportation of synthetic N, ranges from 41.7 to 70.1 Tg CO₂_eq. yr^?1. It was concluded that reducing synthetic N application rate for grain crops in China to a reasonable level of 110–150 kg ha^?1 can greatly reduce the emission of greenhouse gases, especially in the major grain-crop production provinces such as Shandong, Henan, Jiangsu, Hebei, Anhui and Liaoning.     

The fate of nitrogen from incorporated cover crop and green manure residues

Nitrogen retention and release following the incorporation of cover crops and green manures were examined in field trials in NE Scotland. These treatments reduced the amounts of nitrate-N by between 10–20 kg ha^-1 thereby lowering the potential for leaching and gaseous N losses. However, uptake of N by overwintering crops was low, reflecting the short day-lengths and low soil temperatures associated with this part of Britain. Vegetation that had regenerated naturally was as effective as sown cover crops at taking up N over winter and in returning N to the soil for the following crop. Incorporation of residues generally resulted in lower mineralisation rates and reduced N₂O emissions than the cultivation of bare ground, indicating a temporary immobilisation of soil N following incorporation. Emissions from incorporated cover crops ranged from 23–44 g N₂O-N ha^-1 over 19 days, compared with 61 g N₂O-N ha^-1 emitted from bare ground. Emissions from incorporated green manures ranged from 409–580 g N₂O-N ha^-1 over 53 days with 462 g N₂O-N ha^-1 emitted from bare ground. Significant positive correlations between N₂O and soil NO₃ ^- after incorporation (r=0.8–0.9; P<0.001 and r=0.1–0.4; P<0.05 for cover crops and green manures, respectively) suggest that this N₂O was mainly produced during nitrification. There was no significant effect of either cover cropping or green manuring on the N content or yield of the subsequent oats crop, suggesting that N was not sufficiently limiting in this soil for any benefits to become apparent immediately. However, benefits of increased sustainability as a result of increased organic matter concentrations may be seen in long-term organic rotations, and such systems warrant investigation.     

Closing the global N2O budget: nitrous oxide emissions through the agricultural nitrogen cycle

In 1995 a working group was assembled at the request of OECD/IPCC/IEA to revise the methodology for N₂O from agriculture for the National Greenhouse Gas Inventories Methodology. The basics of the methodology developed to calculate annual country level nitrous oxide (N₂O) emissions from agricultural soils is presented herein. Three sources of N₂O are distinguished in the new methodology: (i) direct emissions from agricultural soils, (ii) emissions from animal production, and (iii) N₂O emissions indirectly induced by agricultural activities. The methodology is a simple approach which requires only input data that are available from FAO databases. The methodology attempts to relate N₂O emissions to the agricultural nitrogen (N) cycle and to systems into which N is transported once it leaves agricultural systems. These estimates are made with the realization that increased utilization of crop nutrients, including N, will be required to meet rapidly growing needs for food and fiber production in our immediate future. Anthropogenic N input into agricultural systems include N from synthetic fertilizer, animal wastes, increased biological N-fixation, cultivation of mineral and organic soils through enhanced organic matter mineralization, and mineralization of crop residue returned to the field. Nitrous oxide may be emitted directly to the atmosphere in agricultural fields, animal confinements or pastoral systems or be transported from agricultural systems into ground and surface waters through surface runoff. Nitrate leaching and runoff and food consumption by humans and introduction into sewage systems transport the N ultimately into surface water (rivers and oceans) where additional N₂O is produced. Ammonia and oxides of N (NO_x) are also emitted from agricultural systems and may be transported off-site and serve to fertilize other systems which leads to enhanced production of N₂O. Eventually, all N that moves through the soil system will be either terminally sequestered in buried sediments or denitrified in aquatic systems. We estimated global N₂O–N emissions for the year 1989, using midpoint emission factors from our methodology and the FAO data for 1989. Direct emissions from agricultural soils totaled 2.1 Tg N, direct emissions from animal production totaled 2.1 Tg N and indirect emissions resulting from agricultural N input into the atmosphere and aquatic systems totaled 2.1 Tg N₂O–N for an annual total of 6.3 Tg N₂O–N. The N₂O input to the atmosphere from agricultural production as a whole has apparently been previously underestimated. These new estimates suggest that the missing N₂O sources discussed in earlier IPCC reports is likely a biogenic (agricultural) one.     

Nitrous oxide emissions as influenced by legume cover crops and nitrogen fertilization

In this study, we measured nitrous oxide (N₂O) fluxes from plots of fall-planted hairy vetch (HV, Vicia villosa) and spring-planted broadleaf vetch (BLV, Vicia narbonensis) grown as nitrogen (N) sources for following summer forage crabgrass (Digitaria sanguinalis). Comparisons also included 60 kg ha^?1 inorganic N fertilizer for crabgrass at planting (60-N) and a control without N fertilizer. Each treatment had six replicated plots across the slope. Fluxes were measured with closed chamber systems during the period between spring growth of cover crops and first-cut of crabgrass in mid-July. HV had strong stand and aboveground biomass had 185?±?50 kg N ha^?1 (mean?±?standard error, n?=?6) at termination. However, BLV did not establish well and aboveground biomass had only 35?±?15 kg N ha^?1. Ratio vegetation index of crabgrass measured as proxy of biomass growth was highest in HV treatment. However, total aboveground biomass of crabgrass was statistically similar to 60-N plots. Fluxes of N₂O were low prior to termination of cover crops but were as high as 8.2 kg N₂O ha^?1 day^?1 from HV plots after termination. The fluxes were enhanced by large rainfall events recorded after biomass incorporation. Rainfall enhanced N₂O fluxes were also observed in other treatments, but their magnitudes were much smaller. The high N₂O fluxes from HV plots contributed to emissions of 30.3?±?12.4 kg N₂O ha^?1 within 30 days of biomass incorporation. Emissions were only 2.0?±?0.7, 3.4?±?1.3 and 1.0?±?0.4 kg N₂O ha^?1 from BLV, 60-N and control plots, respectively.     

Effects of fertiliser type and the presence or absence of plants on nitrous oxide emissions from irrigated soils

Nitrous oxide (N₂O) emissions and denitrification losses from an irrigated sandy loam soil amended with composted municipal solid waste (MSW), sheep manure (SM), surface applied pig slurry (SPS), incorporated pig slurry (IPS) or urea (U) were studied under Mediterranean conditions. We quantified emissions, in both the presence and absence of maize and N₂O production, via denitrification and nitrification pathways using varying concentrations of acetylene. Discounting the N₂O lost in the Control, the percentages of N₂O lost in relation to the total N applied were greater for urea (1.80%) than for MSW (0.50%), SM (0.46%), SPS (1.02%) or IPS (1.27%). In general, plots treated with organic fertilisers emitted higher amounts of N₂O when under maize than bare soil plots. On the other hand, greater denitrification losses were also recorded for plots in the absence of plants (between 9.7 and 29.3 kg N₂O-N ha⁻¹) than for areas with plants (between 7.1 and 24.1 kg N₂O-N ha⁻¹). The proportion of N₂O produced via denitrification was greater from fertiliser treatments than for the controls and also greater without plants (between 66 and 91 % of the N₂O emitted) than with plants (between 48 and 81%).     

Root-derived nitrous oxide emissions from an Upper Midwest agricultural ecosystem

Agroecosystems are the dominant source of anthropogenic nitrous oxide (N₂O) emissions globally, yet the partitioning of nitrogen sources supporting N₂O emissions is not well understood. Fertilizer-derived N₂O emissions receive significant attention, while N₂O emissions from organic nitrogen sources, particularly belowground sources, are rarely studied. Here, in situ corn roots (Zea mays L.) were isotopically-labeled with nitrogen (N) and carbon (C) to examine effects of different long-term management systems on root-derived N₂O emissions measured during the following soybean crop in southwest Minnesota, USA. Systems differed in management intensity (tillage and fertilization), crop rotation diversity (two or four crops), and fertilizer type (inorganic or organic). The average contribution of root-derived nitrogen to cumulative N₂O–N emitted over the growing season was 8%, and was higher in 2-year (11%) than 4-year rotations (6%). The fractional loss of root-derived N as N₂O, which is an estimate of the annual emission factor for root-derived N₂O, was small (0.07–0.52%). Management intensity effects on root-derived N₂O emissions and on the root-derived fraction of N₂O emitted differed between two growing seasons as did the effects of fertilizer type on root-derived N cycling rates. Overall, rotation diversity (2 vs. 4-year rotations) exhibited the strongest management effect on root-derived N₂O emissions, suggesting that root-derived N₂O emissions could be mitigated by greater crop rotation diversity.     

Nitrous oxide emissions from an irrigated soil as affected by fertilizer and straw management

Nitrous oxide (N₂O) emission from farmland is a concern for both environmental quality and agricultural productivity. Field experiments were conducted in 1996–1997 to assess soil N₂O emissions as affected by timing of N fertilizer application and straw/tillage practices for crop production under irrigation in southern Alberta. The crops were soft wheat (Triticum aestivumL.) in 1996 and canola (Brassica napusL.) in 1997. Nitrous oxide flux from soil was measured using a vented chamber technique and calculated from the increase in concentration with time. Nitrous oxide fluxes for all treatments varied greatly during the year, with the greatest fluxes occurring in association with freeze-thaw events during March and April. Emissions were greater when N fertilizer (100 kg N ha⁻¹) was applied in the fall compared to spring application. Straw removal at harvest in the fall increased N₂O emissions when N fertilizer was applied in the fall, but decreased emissions when no fertilizer was applied. Fall plowing also increased N₂O emissions compared to spring plowing or direct seeding. The study showed that N₂O emissions may be minimized by applying N fertilizer in spring, retaining straw, and incorporating it in spring. The estimates of regional N₂O emissions based on a fixed proportion of applied N may be tenuous since N₂O emission varied widely depending on straw and fertilizer management practices. This revised version was published online in August 2006 with corrections to the Cover Date.     

Emission of ammonia (NH3), nitrous oxide (N2O) and methane (CH4) from a dairy hardstanding in the UK

Emissions of ammonia (NH₃), nitrous oxide (N₂O) and methane (CH₄) from uncovered yard areas (hardstandings) of a UK dairy farm were measured between October 1997 and August 1999. Measurements were concentrated after morning milking when the yard had been scraped, and at positions accounting for differences in slurry coverage and manure type. Over two seasons, the mean NH₃ emission from a number of season and position categories on the hardstanding were 0.27 g N m⁻² h⁻¹ in winter and spring, 0.45 g N m⁻² h⁻¹ in summer when the feeding/loafing area was not included, increasing to 1.51 g N m⁻² h⁻¹ when this area was included, and 5.0 g N m⁻² h⁻¹ for the feeding/loafing area alone. The feeding/loafing area was close to the slurry lagoon where excreta were continuously deposited and not scraped to the slurry lagoon, as was the rest of the hardstanding. A diurnal study of emissions in the summer showed a marked decrease with time after the yard was scraped following the first milking, with emissions increasing again after evening milking when fresh excreta were deposited. Nitrous oxide emissions were more variable than NH₃, with an order of magnitude difference between lowest and highest emissions measured at the same time. Mean N₂O emission rates were 3.3 μg N m⁻² h⁻¹ in winter and spring, 6.5 μg N m⁻² h⁻¹ in summer when the feeding/loafing area was not included, increasing to 7.8 μg N m⁻² h⁻¹ when this area was included, and 17.9 μg N m⁻² h⁻¹ for the feeding/loafing area alone. Large mean methane emissions were measured, 185 mg C m⁻² h⁻¹ in winter and spring, decreasing to 57.3 mg C m⁻² h⁻¹ in summer when the feeding/loafing area was not included, increasing to 72.9 mg C m⁻² h⁻¹ when this area was included, and 151.2 mg C m⁻² h⁻¹ for the feeding/loafing area alone. Therefore in summer, emissions measured directly from a dung pat [0–5 cm] that had not been scraped from the loafing area were much greater than from scraped hardstanding areas, but in winter there were still significant emissions from the remaining slurry post-scraping. The experimental design was not sufficient to elucidate the physico-chemical variables controlling the measured emissions, but the data were put into context by estimating the annual emission of these pollutant gases from this one dairy farm. These were estimated at 0.43 t NH₃-N y⁻¹, 0.3 kg N₂O-N y⁻¹ and 1.0 kg CH₄-C y⁻¹. Therefore, uncovered farmyard areas that regularly have excreta deposited on them are significant but previously unaccounted for sources of NH₃ loss, less so for N₂O and CH₄, and require further study to assess the significance of these emission sources within the UK and worldwide. This revised version was published online in August 2006 with corrections to the Cover Date.     

Comparing a process-based agro-ecosystem model to the IPCC methodology for developing a national inventory of N2O emissions from arable lands in China

Nations are now obligated to assess their greenhouse gas emissions under the protocols of Article 4 of the United Nations Framework Convention on Climate Change. The IPCC has developed `spreadsheet-format' methodologies for countries to estimate national greenhouse gas emissions by economic sector. Each activity has a magnitude and emission rate and their product is summed over all included activities to generate a national total (IPCC, 1997). For N₂O emissions from cropland soils, field studies have shown that there are important factors that influence N₂O emissions at specific field sites that are not considered in the IPCC methodology. We used DNDC, a process-oriented agroecosystem model, to develop an unofficial national inventory of direct N₂O emissions from cropland in China. We assembled county-scale data on soil properties, daily weather, crop areas, N-fertilizer use, livestock populations (for manure inputs to cropland), and agricultural management for the 2500 counties in mainland China. Total 1990 cropland area was 0.95 million km². Total N-fertilizer use in China in 1990 was 16.6 Tg N. The average fertilization rate was 175 kg N ha⁻¹ cropland. One-year simulations with DNDC were run for each crop type in each county to generate estimates of direct N₂O emissions from soils. National totals were the sum of results for all crop simulations across all counties. Baseline simulations estimated that total N₂O emission from arable land in China in 1990 was 0.31 Tg N₂O-N yr⁻¹. We also ran simulations with zero N-fertilizer input; the difference between the zero-fertilizer and the baseline run is an estimate of fertilizer-induced N₂O emissions. The fertilizer-induced emission was 0.13 Tg N₂O-N yr⁻¹, about 0.8% of total N-fertilizer use (lower than the mean but within the IPCC range of 1.25±1.0%). We compared these results to our estimates of county-scale IPCC methodology emissions. Total emissions were similar but geographical patterns were quite different. This revised version was published online in August 2006 with corrections to the Cover Date.     

Soil N2O and CO2 emissions from cotton in Australia under varying irrigation management

Irrigation is known to stimulate soil microbial carbon and nitrogen turnover and potentially the emissions of nitrous oxide (N₂O) and carbon dioxide (CO₂). We conducted a study to evaluate the effect of three different irrigation intensities on soil N₂O and CO₂ fluxes and to determine if irrigation management can be used to mitigate N₂O emissions from irrigated cotton on black vertisols in South-Eastern Queensland, Australia. Fluxes were measured over the entire 2009/2010 cotton growing season with a fully automated chamber system that measured emissions on a sub-daily basis. Irrigation intensity had a significant effect on CO₂ emission. More frequent irrigation stimulated soil respiration and seasonal CO₂ fluxes ranged from 2.7 to 4.1 Mg-C ha^?1 for the treatments with the lowest and highest irrigation frequency, respectively. N₂O emission happened episodic with highest emissions when heavy rainfall or irrigation coincided with elevated soil mineral N levels and seasonal emissions ranged from 0.80 to 1.07 kg N₂O-N ha^?1 for the different treatments. Emission factors (EF = proportion of N fertilizer emitted as N₂O) over the cotton cropping season, uncorrected for background emissions, ranged from 0.40 to 0.53 % of total N applied for the different treatments. There was no significant effect of the different irrigation treatments on soil N₂O fluxes because highest emission happened in all treatments following heavy rainfall caused by a series of summer thunderstorms which overrode the effect of the irrigation treatment. However, higher irrigation intensity increased the cotton yield and therefore reduced the N₂O intensity (N₂O emission per lint yield) of this cropping system. Our data suggest that there is only limited scope to reduce absolute N₂O emissions by different irrigation intensities in irrigated cotton systems with summer dominated rainfall. However, the significant impact of the irrigation treatments on the N₂O intensity clearly shows that irrigation can easily be used to optimize the N₂O intensity of such a system.     

Fungal and bacterial contributions to codenitrification emissions of N<Subscript>2</Subscript>O and N<Subscript>2</Subscript> following urea deposition to soil

Grazed pastures contribute significantly to anthropogenic emissions of N₂O but the respective contributions of archaea, bacteria and fungi to codenitrification in such systems is unresolved. This study examined the relative contributions of bacteria and fungi to rates of denitrification and codenitrification under a simulated ruminant urine event. It was hypothesised that fungi would be primarily responsible for both codenitrification and total N₂O and N₂ emissions. The effects of bacterial (streptomycin), fungal (cycloheximide), and combined inhibitor treatments were measured in a laboratory mesocosm experiment, on soil that had received ¹⁵N labelled urea. Soil inorganic-N concentrations, N₂O and N₂ gas fluxes were measured over 51 days. On Days 42 and 51, when nitrification was actively proceeding in the positive control, the inhibitor treatments inhibited nitrification as evidenced by increased soil NH ₄ ⁺ -N concentrations and decreased soil NO ₂ ^? -N and NO ₃ ^? -N concentrations. Codenitrification was observed to contribute to total fluxes of both N₂O (≥ 33%) and N₂ (≥ 3%) in urine-amended grassland soils. Cycloheximide inhibition decreased NH ₄ ⁺ –¹⁵N enrichment and reduced N₂O fluxes while reducing the contribution of codenitrification to total N₂O fluxes by ≥ 66 and ≥ 42%, respectively. Thus, given archaea do not respond to significant urea deposition, it is proposed that fungi, not bacteria, dominated total N₂O fluxes, and the codenitrification N₂O fluxes, from a simulated urine amended pasture soil.