Soil‐derived trace gas fluxes from different energy crops – results from a field experiment in Southwest Germany

Willow coppice, energy maize and Miscanthus were evaluated regarding their soil‐derived trace gas emission potential involving a nonfertilized and a crop‐adapted slow‐release nitrogen (N) fertilizer scheme. The N application rate was 80 kg N ha^?1 yr^?1 for the perennial crops and 240 kg N ha^?1 yr^?1 for the annual maize. A replicated field experiment was conducted with 1‐year measurements of soil fluxes of CH₄, CO₂ and N₂O in weekly intervals using static chambers. The measurements revealed a clear seasonal trend in soil CO₂ emissions, with highest emissions being found for the N‐fertilized Miscanthus plots (annual mean: 50 mg C m^?² h^?1). Significant differences between the cropping systems were found in soil N₂O emissions due to their dependency on amount and timing of N fertilization. N‐fertilized maize plots had highest N₂O emissions by far, which accumulated to 3.6 kg N₂O ha^?1 yr^?1. The contribution of CH₄ fluxes to the total soil greenhouse gas subsumption was very small compared with N₂O and CO₂. CH₄ fluxes were mostly negative indicating that the investigated soils mainly acted as weak sinks for atmospheric CH₄. To identify the system providing the best ratio of yield to soil N₂O emissions, a subsumption relative to biomass yields was calculated. N‐fertilized maize caused the highest soil N₂O emissions relative to dry matter yields. Moreover, unfertilized maize had higher relative soil N₂O emissions than unfertilized Miscanthus and willow. These results favour perennial crops for bioenergy production, as they are able to provide high yields with low N₂O emissions in the field.     

Nonlinear response of N2O flux to incremental fertilizer addition in a continuous maize (Zea mays L.) cropping system

The relationship between nitrous oxide (N₂O) flux and N availability in agricultural ecosystems is usually assumed to be linear, with the same proportion of nitrogen lost as N₂O regardless of input level. We conducted a 3‐year, high‐resolution N fertilizer response study in southwest Michigan USA to test the hypothesis that N₂O fluxes increase mainly in response to N additions that exceed crop N needs. We added urea ammonium nitrate or granular urea at nine levels (0–292 kg N ha^?1) to four replicate plots of continuous maize. We measured N₂O fluxes and available soil N biweekly following fertilization and grain yields at the end of the growing season. From 2001 to 2003 N₂O fluxes were moderately low (ca. 20 g N₂O‐N ha^?1 day^?1) at levels of N addition to 101 kg N ha^?1, where grain yields were maximized, after which fluxes more than doubled (to >50 g N₂O‐N ha^?1 day^?1). This threshold N₂O response to N fertilization suggests that agricultural N₂O fluxes could be reduced with no or little yield penalty by reducing N fertilizer inputs to levels that just satisfy crop needs.     

Impacts of climate and land use on N2O and CH4 fluxes from tropical ecosystems in the Mt. Kilimanjaro region,Tanzania

In this study, we quantify the impacts of climate and land use on soil N₂O and CH₄ fluxes from tropical forest, agroforest, arable and savanna ecosystems in Africa. To do so, we measured greenhouse gases (GHG) fluxes from 12 different ecosystems along climate and land‐use gradients at Mt. Kilimanjaro, combining long‐term in situ chamber and laboratory soil core incubation techniques. Both methods showed similar patterns of GHG exchange. Although there were distinct differences from ecosystem to ecosystem, soils generally functioned as net sources and sinks for N₂O and CH₄ respectively. N₂O emissions correlated positively with soil moisture and total soil nitrogen content. CH₄ uptake rates correlated negatively with soil moisture and clay content and positively with SOC. Due to moderate soil moisture contents and the dominance of nitrification in soil N turnover, N₂O emissions of tropical montane forests were generally low (<1.2 kg N ha^?1 year^?1), and it is likely that ecosystem N losses are driven instead by nitrate leaching (~10 kg N ha^?1 year^?1). Forest soils with well‐aerated litter layers were a significant sink for atmospheric CH₄ (up to 4 kg C ha^?1 year^?1) regardless of low mean annual temperatures at higher elevations. Land‐use intensification significantly increased the soil N₂O source strength and significantly decreased the soil CH₄ sink. Compared to decreases in aboveground and belowground carbon stocks enhanced soil non‐CO₂ GHG emissions following land‐use conversion from tropical forests to homegardens and coffee plantations were only a small factor in the total GHG budget. However, due to lower ecosystem carbon stock changes, enhanced N₂O emissions significantly contributed to total GHG emissions following conversion of savanna into grassland and particularly maize. Overall, we found that the protection and sustainable management of aboveground and belowground carbon and nitrogen stocks of agroforestry and arable systems is most crucial for mitigating GHG emissions from land‐use change.     

Predicting N2O emissions from agricultural land through related soil parameters

An empirical model of nitrous oxide emission from agricultural soils has been developed. It is based on the relationship between N₂O and three soil parameters – soil mineral N (ammonium plus nitrate) content in the topsoil, soil water‐filled pore space and soil temperature – determined in a study on a fertilized grassland in 1992 and 1993. The model gave a satisfactory prediction of seasonal fluxes in other seasons when fluxes were much higher, and also from other grassland sites and from cereal and oilseed rape crops, over a wide flux range (< 1 to > 20 kg N₂O‐N ha^?1 y^?1). However, the model underestimated emissions from potato and broccoli crops; possible reasons for this are discussed. This modelling approach, based as it is on well‐established and widely used soil measurements, has the potential to provide flux estimates from a much wider range of agricultural sites than would be possible by direct measurement of N₂O emissions.     

Soil nitrous oxide and methane fluxes are low from a bioenergy crop (canola) grown in a semi-arid climate

Understanding nitrous oxide (N₂O) and methane (CH₄) fluxes from agricultural soils in semi‐arid climates is necessary to fully assess greenhouse gas emissions from bioenergy cropping systems, and to improve our knowledge of global terrestrial gaseous exchange. Canola is grown globally as a feedstock for biodiesel production, however, resulting soil greenhouse gas fluxes are rarely reported for semi‐arid climates. We measured soil N₂O and CH₄ fluxes from a rain‐fed canola crop in a semi‐arid region of south‐western Australia for 1 year on a subdaily basis. The site included N fertilized (75 kg N ha^?1 yr^?1) and nonfertilized plots. Daily N₂O fluxes were low (?1.5 to 4.7 g N₂O‐N ha^?1 day^?1) and culminated in an annual loss of 128 g N₂O‐N ha^?1 (standard error, 12 g N₂O‐N ha^?1) from N fertilized soil and 80 g N₂O‐N ha^?1 (standard error, 11 g N₂O‐N ha^?1) from nonfertilized soil. Daily CH₄ fluxes were also low (?10.3 to 11.9 g CH₄‐C ha^?1 day^?1), and did not differ with treatments, with an average annual net emission of 6.7 g CH₄–C ha^?1 (standard error, 20 g CH₄–C ha^?1). Greatest daily N₂O fluxes occurred when the soil was fallow, and following a series of summer rainfall events. Summer rainfall increased soil water contents and available N, and occurred when soil temperatures were >25 °C, and when there was no active plant growth to compete with soil microorganisms for mineralized N; conditions known to promote N₂O production. The proportion of N fertilizer emitted as N₂O, after correction for emissions from the no N fertilizer treatment, was 0.06%; 17 times lower than IPCC default value for the application of synthetic N fertilizers to land (1.0%). Soil greenhouse gas fluxes from bioenergy crop production in semi‐arid regions are likely to have less influence on the net global warming potential of biofuel production than in temperate climates.     

Environmental factors controlling temporal and spatial variability in the soil‐atmosphere exchange of CO2, CH4 and N2O from an Australian subtropical rainforest

The temporal variations in CO₂, CH₄ and N₂O fluxes were measured over two consecutive years from February 2007 to March 2009 from a subtropical rainforest in south‐eastern Queensland, Australia, using an automated sampling system. A concurrent study using an additional 30 manual chambers examined the spatial variability of emissions distributed across three nearby remnant rainforest sites with similar vegetation and climatic conditions. Interannual variation in fluxes of all gases over the 2 years was minimal, despite large discrepancies in rainfall, whereas a pronounced seasonal variation could only be observed for CO₂ fluxes. High infiltration, drainage and subsequent high soil aeration under the rainforest limited N₂O loss while promoting substantial CH₄ uptake. The average annual N₂O loss of 0.5 ± 0.1 kg N₂O‐N ha^?1 over the 2‐year measurement period was at the lower end of reported fluxes from rainforest soils. The rainforest soil functioned as a sink for atmospheric CH₄ throughout the entire 2‐year period, despite periods of substantial rainfall. A clear linear correlation between soil moisture and CH₄ uptake was found. Rates of uptake ranged from greater than 15 g CH₄‐C ha^?1 day^?1 during extended dry periods to less than 2–5 g CH₄‐C ha^?1 day^?1 when soil water content was high. The calculated annual CH₄ uptake at the site was 3.65 kg CH₄‐C ha^?1 yr^?1. This is amongst the highest reported for rainforest systems, reiterating the ability of aerated subtropical rainforests to act as substantial sinks of CH₄. The spatial study showed N₂O fluxes almost eight times higher, and CH₄ uptake reduced by over one‐third, as clay content of the rainforest soil increased from 12% to more than 23%. This demonstrates that for some rainforest ecosystems, soil texture and related water infiltration and drainage capacity constraints may play a more important role in controlling fluxes than either vegetation or seasonal variability.     

Nitrous oxide fluxes from corn fields: on-farm assessment of the amount and timing of nitrogen fertilizer

Nitrogen fertilization is considered as an important source of atmospheric N₂O emission. A seven site‐year on‐farm field experiment was conducted at Ottawa and Guelph, ON and Saint‐Valentin, QC, Canada to characterize the affect of the amount and timing of N fertilizer on N₂O emission in corn (Zea mays L.) production. Using the static chamber method, gas samples were collected for 28‐days after preplant and 28‐days after sidedress fertilization at the seven site‐year, resulting in 14 monitoring periods. For both methods of fertilization, peak N₂O flux and cumulative emission increased with the amount of N applied, with rates ranging from 30 to 900 μg N m^?2 h^?1. Depending on N amount and time of application, cumulative emission varied from 0.05 to 2.42 kg N ha^?1, equivalent to 0.03% to 1.45% of the N fertilizer applied. Differences in N₂O emission peaks among fertilizer treatments were clearly separated in 13 out of 14 monitoring periods. Total N₂O emissions may have been underestimated compared with annual monitoring in 10 out of the 49 cases because the monitoring period ended before N₂O efflux returned to the baseline level. The flux of N₂O was negligible when soil mineral N in the 0–15 cm layer was < 20 mg N kg^?1. While rainfall stimulated emission, soil temperature > 15 °C was likely the driving force responsible for the higher levels of N₂O found for sidedress than preplant application methods. However, caution must be taken when interpreting these later results as preplant fertilization may have continuously stimulated N₂O emissions after the 28‐days monitoring period, especially in situations where N₂O effluxes have not fallen back to their baseline levels. Increasing fertilizer rates from 90 to 150 kg N ha^?1 resulted in slight increases in yields, but doubled cumulative N₂O emissions.     

Nonlinear nitrous oxide (N2O) response to nitrogen fertilizer in on‐farm corn crops of the US Midwest

Row‐crop agriculture is a major source of nitrous oxide (N₂O) globally, and results from recent field experiments suggest that significant decreases in N₂O emissions may be possible by decreasing nitrogen (N) fertilizer inputs without affecting economic return from grain yield. We tested this hypothesis on five commercially farmed fields in Michigan, USA planted with corn in 2007 and 2008. Six rates of N fertilizer (0–225 kg N ha^?1) were broadcast and incorporated before planting, as per local practice. Across all sites and years, increases in N₂O flux were best described by a nonlinear, exponentially increasing response to increasing N rate. N₂O emission factors per unit of N applied ranged from 0.6% to 1.5% and increased with increasing N application across all sites and years, especially at N rates above those required for maximum crop yield. At the two N fertilizer rates above those recommended for maximum economic return (135 kg N ha^?1), average N₂O fluxes were 43% (18 g N₂O–N ha^?1 day^?1) and 115% (26 g N₂O–N ha^?1 day^?1) higher than were fluxes at the recommended rate, respectively. The maximum return to nitrogen rate of 154 kg N ha^?1 yielded an average 8.3 Mg grain ha^?1. Our study shows the potential to lower agricultural N₂O fluxes within a range of N fertilization that does not affect economic return from grain yield.     

Nitrous oxide fluxes from a grain–legume crop (narrow‐leafed lupin) grown in a semiarid climate

Understanding nitrous oxide (N₂O) fluxes from grain–legume crops in semiarid and arid regions is necessary if we are to improve our knowledge of global terrestrial N₂O losses resulting from biological N₂ fixation. N₂O fluxes were measured from a rain‐fed soil, cropped to a grain–legume in a semiarid region of southwestern Australia for 1 year on a subdaily basis. The site included plots planted to narrow‐leafed lupin (Lupinus angustifolius; ‘lupin’) and plots left bare (no lupin). Fluxes were measured using soil chambers connected to a fully automated system that measured N₂O by gas chromatography. Daily N₂O fluxes were low (?0.5 to 24 g N₂O‐N ha^?1 day^?1) and not different between treatments, culminating in an annual loss of 127 g N₂O‐N ha^?1. Greatest daily N₂O fluxes occurred from both treatments in the postharvest period, and following a series of summer and autumn rainfall events. At this time of the year, soil conditions were conducive to soil microbial N₂O production: elevated soil water contents, increased inorganic nitrogen (N) and dissolved organic carbon concentrations, and soil temperatures generally > 25 °C; furthermore, there was no active plant growth to compete for mineralized N. N₂O emissions from the decomposition of legume crop residue were low, and approximately half that predicted using the currently recommended IPCC methodology. Furthermore, the contribution of the biological N₂ fixation process to N₂O emissions appeared negligible in the present study, supporting its omission as a source of N₂O from the IPCC methodology for preparing national greenhouse gas inventories.     

Greenhouse gas fluxes from an Australian subtropical cropland under long‐term contrasting management regimes

The long‐term effects of conservation management practices on greenhouse gas fluxes from tropical/subtropical croplands remain to be uncertain. Using both manual and automatic sampling chambers, we measured N₂O and CH₄ fluxes at a long‐term experimental site (1968–present) in Queensland, Australia from 2006 to 2009. Annual net greenhouse gas fluxes (NGGF) were calculated from the 3‐year mean N₂O and CH₄ fluxes and the long‐term soil organic carbon changes. N₂O emissions exhibited clear daily, seasonal and interannual variations, highlighting the importance of whole‐year measurement over multiple years for obtaining temporally representative annual emissions. Averaged over 3 years, annual N₂O emissions from the unfertilized and fertilized soils (90 kg N ha^?1 yr^?1 as urea) amounted to 138 and 902 g N ha^?1, respectively. The average annual N₂O emissions from the fertilized soil were 388 g N ha^?1 lower under no‐till (NT) than under conventional tillage (CT) and 259 g N ha^?1 higher under stubble retention (SR) than under stubble burning (SB). Annual N₂O emissions from the unfertilized soil were similar between the contrasting tillage and stubble management practices. The average emission factors of fertilizer N were 0.91%, 1.20%, 0.52% and 0.77% for the CT‐SB, CT‐SR, NT‐SB and NT‐SR treatments, respectively. Annual CH₄ fluxes from the soil were very small (?200–300 g CH₄ ha^?1 yr^?1) with no significant difference between treatments. The NGGF were 277–350 kg CO₂‐e ha^?1 yr^?1 for the unfertilized treatments and 401–710 kg CO₂‐e ha^?1 yr^?1 for the fertilized treatments. Among the fertilized treatments, N₂O emissions accounted for 52–97% of NGGF and NT‐SR resulted in the lowest NGGF (401 kg CO₂‐e ha^?1 yr^?1 or 140 kg CO₂‐e t^?1 grain). Therefore, NT‐SR with improved N fertilizer management practices was considered the most promising management regime for simultaneously achieving maximal yield and minimal NGGF.     

Nitrous oxide emissions from a cropped soil in a semi-arid climate

Understanding nitrous oxide (N₂O) emissions from agricultural soils in semi‐arid regions is required to better understand global terrestrial N₂O losses. Nitrous oxide emissions were measured from a rain‐fed, cropped soil in a semi‐arid region of south‐western Australia for one year on a sub‐daily basis. The site included N‐fertilized (100 kg N ha^?1 yr^?1) and nonfertilized plots. Emissions were measured using soil chambers connected to a fully automated system that measured N₂O using gas chromatography. Daily N₂O emissions were low (?1.8 to 7.3 g N₂O‐N ha^?1 day^?1) and culminated in an annual loss of 0.11 kg N₂O‐N ha^?1 from N‐fertilized soil and 0.09 kg N₂O‐N ha^?1 from nonfertilized soil. Over half (55%) the annual N₂O emission occurred from both N treatments when the soil was fallow, following a series of summer rainfall events. At this time of the year, conditions were conducive for soil microbial N₂O production: elevated soil water content, available N, soil temperatures generally >25 °C and no active plant growth. The proportion of N fertilizer emitted as N₂O in 1 year, after correction for the ‘background’ emission (no N fertilizer applied), was 0.02%. The emission factor reported in this study was 60 times lower than the IPCC default value for the application of synthetic fertilizers to land (1.25%), suggesting that the default may not be suitable for cropped soils in semi‐arid regions. Applying N fertilizer did not significantly increase the annual N₂O emission, demonstrating that a proportion of N₂O emitted from agricultural soils may not be directly derived from the application of N fertilizer. ‘Background’ emissions, resulting from other agricultural practices, need to be accounted for if we are to fully assess the impact of agriculture in semi‐arid regions on global terrestrial N₂O emissions.     

氮素类型和剂量对寒温带针叶林土壤N2O排放的影响

大气氮沉降输入会增加森林生态系统氮素有效性,进而改变土壤N_2O产生与排放,然而有关不同氮素离子(氧化态NO_3~--N与还原态NH_4~+-N)沉降对土壤N_2O排放的影响知之甚少。以大兴安岭寒温带针叶林为研究对象,构建了3种类型(NH_4Cl、KNO_3、NH_4NO_3)和4个施氮水平(0、10、20、40 kg N hm~(-2)a~(-1))的增氮控制试验,利用流动化学分析仪和静态箱-气相色谱法4次/月测定凋落物层和矿质层土壤无机氮含量、土壤-大气界面N_2O净交换通量以及相关环境因子,分析施氮类型和剂量对土壤氮素有效性、土壤N_2O通量的影响探讨氮素富集条件下土壤N_2O通量的环境驱动机制。结果表明:施氮类型和剂量均显著影响土壤无机氮含量,土壤NH_4~+-N的积累效应显著高于NO_3~--N。施氮一致增加寒温带针叶林土壤N_2O排放,NH_4NO_3促进效应最为明显,增幅为442%-677%,高于全球平均水平(134%)。土壤N_2O通量与土壤温度、凋落物层NH_4~+-N含量正相关,且随着施氮水平增加而增加。结果表明大气氮沉降短期内不会导致寒温带针叶林土壤NO_3~--N大量流失,但会显著促进土壤N_2O的排放。此外,外源性NH_4~+和NO_3~-输入对土壤N_2O排放的促进作用具有协同效应,在未来森林生态系统氮循环和氮平衡研究中应该区分对待。     

Soil-atmospheric exchange of CO2, CH4, and N2O in three subtropical forest ecosystems in southern China

The magnitude, temporal, and spatial patterns of soil‐atmospheric greenhouse gas (hereafter referred to as GHG) exchanges in forests near the Tropic of Cancer are still highly uncertain. To contribute towards an improvement of actual estimates, soil‐atmospheric CO₂, CH₄, and N₂O fluxes were measured in three successional subtropical forests at the Dinghushan Nature Reserve (hereafter referred to as DNR) in southern China. Soils in DNR forests behaved as N₂O sources and CH₄ sinks. Annual mean CO₂, N₂O, and CH₄ fluxes (mean±SD) were 7.7±4.6 Mg CO₂‐C ha^?1 yr^?1, 3.2±1.2 kg N₂O‐N ha^?1 yr^?1, and 3.4±0.9 kg CH₄‐C ha^?1 yr^?1, respectively. The climate was warm and wet from April through September 2003 (the hot‐humid season) and became cool and dry from October 2003 through March 2004 (the cool‐dry season). The seasonality of soil CO₂ emission coincided with the seasonal climate pattern, with high CO₂ emission rates in the hot‐humid season and low rates in the cool‐dry season. In contrast, seasonal patterns of CH₄ and N₂O fluxes were not clear, although higher CH₄ uptake rates were often observed in the cool‐dry season and higher N₂O emission rates were often observed in the hot‐humid season. GHG fluxes measured at these three sites showed a clear increasing trend with the progressive succession. If this trend is representative at the regional scale, CO₂ and N₂O emissions and CH₄ uptake in southern China may increase in the future in light of the projected change in forest age structure. Removal of surface litter reduced soil CO₂ effluxes by 17–44% in the three forests but had no significant effect on CH₄ absorption and N₂O emission rates. This suggests that microbial CH₄ uptake and N₂O production was mainly related to the mineral soil rather than in the surface litter layer.     

Control of Nitrous Oxide Emissions in European Beech,Norway Spruce and Scots Pine Forests

Elevated nitrogen deposition has increased tree growth, the storage of soil organic matter, and nitrate leaching in many European forests, but little is known about the effect of tree species and nitrogen deposition on nitrous oxide emission. Here we report soil N₂O emission from European beech, Scots pine and Norway spruce forests in two study areas of Germany with distinct climate, N deposition and soils. N₂O emissions and throughfall input of nitrate and ammonium were measured biweekly during growing season and monthly during dormant season over a 28 months period. Annual N₂O emission rates ranged between 0.4 and 1.3 kg N ha^?1 year^?1 among the stands and were higher in 1998 than in 1999 due to higher precipitation during the growing season of 1998. A 2-way-ANOVA revealed that N₂O fluxes were significantly higher (p<0.001) at Solling than at Unterlüß while tree species had no effect on N₂O emissions. Soil texture and the amount of throughfall explained together 94% of the variance among the stands, indicating that increasing portions of silt and clay may promote the formation of N₂O in wet forest soils. Moreover, cumulative N₂O fluxes were significantly correlated (r² = 0.60, p<0.001) with cumulative NO ₃ ^? fluxes at 10 cm depth as an indicator of N saturation, however, the slope of the regression curve indicates a rather weak effect of NO ₃ ^? fluxes on N₂O emissions. N input by throughfall was not correlated with N₂O emissions and only 1.6–3.2% of N input was released as N₂O to the atmosphere. Our results suggest that elevated N inputs have little effect on N₂O emissions in beech, spruce and pine forests.     

Nitrogen loss from grassland on peat soils through nitrous oxide production

Nitrous oxide (N₂O) in soils is produced through nitrification and denitrification. The N₂O produced is considered as a nitrogen (N) loss because it will most likely escape from the soil to the atmosphere as N₂O or N₂. Aim of the study was to quantify N₂O production in grassland on peat soils in relation to N input and to determine the relative contribution of nitrification and denitrification to N₂O production. Measurements were carried out on a weekly basis in 2 grasslands on peat soil (Peat I and Peat II) for 2 years (1993 and 1994) using intact soil core incubations. In additional experiments distinction between N₂O from nitrification and denitrification was made by use of the gaseous nitrification inhibitor methyl fluoride (CH₃F).Nitrous oxide production over the 2 year period was on average 34 kg N ha^-1 yr^-1 for mown treatments that received no N fertiliser and 44 kg N ha^-1 yr^-1 for mown and N fertilised treatments. Grazing by dairy cattle on Peat I caused additional N₂O production to reach 81 kg N ha^-1 yr^-1. The sub soil (20–40 cm) contributed 25 to 40% of the total N₂O production in the 0–40 cm layer. The N₂O production:denitrification ratio was on average about 1 in the top soil and 2 in the sub soil indicating that N₂O production through nitrification was important. Experiments showed that when ratios were larger than l, nitrification was the major source of N₂O. In conclusion, N₂O production is a significant N loss mechanism in grassland on peat soil with nitrification as an important N₂O producing process.     

Nitrous oxide emission factors for agricultural soils in Great Britain: the impact of soil water-filled pore space and other controlling variables

Measurements were made of nitrous oxide (N₂O) emissions from N‐fertilised ungrazed grassland and arable land at sites widely distributed across Great Britain during 1999–2001. The closed static chamber method was used throughout. Emissions varied widely throughout the year at each site, and between sites. Daily fluxes up to 1200 g N₂O–N ha ^{? 1} d ^{? 1} were recorded. The highest annual flux was 27.6 kg N₂O–N ha ^{? 1} at a grassland site in Wales, whereas the lowest, 1.7 kg N₂O–N ha ^{? 1}, occurred on a soil overlying chalk in southern England. The key factors affecting N₂O emissions from agricultural soil were soil WFPS, temperature and soil NO₃^––N content. On grassland, rainfall (particularly around the time of N application), with its consequent effect on water‐filled pore space (WFPS), was the main driving factor during the growing season. Annual emission factors (EFs), uncorrected for background emission, varied from 0.4 to 6.5% of the nitrogen (N) applied, covering a similar range for grassland to that found previously for sites restricted to Scotland. Continued monitoring at a grassland reference site near Edinburgh showed that annual EFs vary greatly from year to year, even with similar management, and that several years' data are required to produce a robust mean EF. The overall distribution of EFs in this and previous studies was log‐normal. The EFs for small‐grain cereals (and oilseed rape) peaked at a much lower value than those for grassland, whereas the values for leafy vegetables and potato crops fitted well into the grassland distribution. These differences in EF between various types of crop should be taken into account when compiling regional or national N₂O emission inventories.     

Drought-induced nitrous oxide flux dynamics in an enclosed tropical forest

El Niño–La Niña cycles strongly influence dry and wet seasons in the tropics and consequently nitrous oxide (N₂O) emissions from tropical rainforest soils. We monitored whole‐system and soil chamber N₂O fluxes during 5‐month‐long droughts in the Biosphere 2 tropical forest to determine how rainfall changes N₂O production. A consistent pattern of N₂O flux changes during drought and subsequent wetting emerged from our experiments. Soil surface drying during the first days of drought, presumably increased gas transport out of the soil, which increased N₂O fluxes. Subsequent drying caused an exponential decrease in whole‐system (4.0±0.1% day^?1) and soil chamber N₂O flux (8.9±0.8% day^?1; south chamber; and 13.7±1.1% day^?1; north chamber), which was highly correlated with soil moisture content. Soil air N₂O concentration ([N₂O]) and flux measurements revealed that surface N₂O production persisted during drought. The first rainfall after drought triggered a N₂O pulse, which amounted to 25% of drought‐associated reduction in N₂O flux and 1.3±0.4% of annual N₂O emissions. Physical displacement of soil air by water and soil chemistry changes during drought could not account for the observed N₂O pulse. We contend that osmotic stress on the microbial biomass must have supplied the N source for pulse N₂O, which was produced at the litter–soil interface. After the pulse, N₂O fluxes were consistently 90% of predrought values. Nitrate change rate, nutrient, [N₂O], and flux analyses suggested that nitrifiers dominated N₂O production during the pulse and denitrifiers during wet conditions. N₂O flux measurements in Biosphere 2, especially during the N₂O pulse, demonstrate that large‐scale integration methods, such as flux towers, are essential for improving ecosystem N₂O flux estimates.     

Regional application of PnET-N-DNDC for estimating the N2O source strength of tropical rainforests in the Wet Tropics of Australia

In contrast to the significant importance of tropical rainforest ecosystems as one of the major sources within the global atmospheric N₂O budget (2.2–3.7 Tg N yr^?1), regional estimates of their N₂O source strength are still limited and highly uncertain. To contribute toward more reliable estimates of the N₂O source strength of tropical rainforest ecosystems on a regional scale, we modified a process‐oriented biogeochemical model, PnET‐N‐DNDC, and parameterized it to simulate C and N turnover and associated N₂O emissions in and from tropical rainforest ecosystems. Model modifications included: (1) new parameterizations associated with plant physiology and soil hydrology and the addition of algorithms relating daily leaf litterfall to water stress as well as to daily rainfall to account for the effects of heavy rainfall damage; (2) the development of a denitrifier activity index that depends on soil moisture conditions and influences N turnover by denitrification; and (3) the addition of a biological N fixation algorithm. Daily simulated N₂O emissions based on site data were in good agreement (model efficiencies up to 0.83) with field observations in the Wet Tropics of Australia and Costa Rica. The model was even able to reproduce the highly dynamic pattern of N₂O emissions with short‐term increases during the wet season. Sensitivity analyses demonstrated that the PnET‐N‐DNDC model was sensitive to changes in soil properties such as pH, clay content, soil organic carbon and climatic factors such as rainfall and temperature. By linking the PnET‐N‐DNDC model to a geographic information systems database, tropical rainforests in a 9000 km² area of the Wet Tropics of Australia are estimated to emit 962 t N₂O‐N yr^?1 (2.4 kg N₂O‐N ha^?1 yr^?1) between July 1997 and June 1998.     

Initial cultivation of a temperate-region soil immediately accelerates aggregate turnover and CO2 and N2O fluxes

The immediate effects of tillage on protected soil C and N pools and on trace gas emissions from soils at precultivation levels of native C remain largely unknown. We measured the response to cultivation of CO₂ and N₂O emissions and associated environmental factors in a previously uncultivated U.S. Midwest Alfisol with C concentrations that were indistinguishable from those in adjacent late successional forests on the same soil type (3.2%). Within 2 days of initial cultivation in 2002, tillage significantly (P=0.001, n=4) increased CO₂ fluxes from 91 to 196 mg CO₂‐C m^?2 h^?1 and within the first 30 days higher fluxes because of cultivation were responsible for losses of 85 g CO₂‐C m^?2. Additional daily C losses were sustained during a second and third year of cultivation of the same plots at rates of 1.9 and 1.0 g C m^?2 day^?1, respectively. Associated with the CO₂ responses were increased soil temperature, substantially reduced soil aggregate size (mean weight diameter decreased 35% within 60 days), and a reduction in the proportion of intraaggregate, physically protected light fraction organic matter. Nitrous oxide fluxes in cultivated plots increased 7.7‐fold in 2002, 3.1‐fold in 2003, and 6.7‐fold in 2004 and were associated with increased soil NO₃^? concentrations, which approached 15 μg N g^?1. Decreased plant N uptake immediately after tillage, plus increased mineralization rates and fivefold greater nitrifier enzyme activity, likely contributed to increased NO₃^? concentrations. Our results demonstrate that initial cultivation of a soil at precultivation levels of native soil C immediately destabilizes physical and microbial processes related to C and N retention in soils and accelerates trace gas fluxes. Policies designed to promote long‐term C sequestration may thus need to protect soils from even occasional cultivation in order to preserve sequestered C.     

Soil 13C–15N dynamics in an N2-fixing clover system under long-term exposure to elevated atmospheric CO2

Reduced soil N availability under elevated CO₂ may limit the plant's capacity to increase photosynthesis and thus the potential for increased soil C input. Plant productivity and soil C input should be less constrained by available soil N in an N₂‐fixing system. We studied the effects of Trifolium repens (an N₂‐fixing legume) and Lolium perenne on soil N and C sequestration in response to 9 years of elevated CO₂ under FACE conditions. ¹⁵N‐labeled fertilizer was applied at a rate of 140 and 560 kg N ha^?1 yr^?1 and the CO₂ concentration was increased to 60 Pa pCO₂ using ¹³C‐depleted CO₂. The total soil C content was unaffected by elevated CO₂, species and rate of ¹⁵N fertilization. However, under elevated CO₂, the total amount of newly sequestered soil C was significantly higher under T. repens than under L. perenne. The fraction of fertilizer‐N (f_N) of the total soil N pool was significantly lower under T. repens than under L. perenne. The rate of N fertilization, but not elevated CO₂, had a significant effect on f_N values of the total soil N pool. The fractions of newly sequestered C (f_C) differed strongly among intra‐aggregate soil organic matter fractions, but were unaffected by plant species and the rate of N fertilization. Under elevated CO₂, the ratio of fertilizer‐N per unit of new C decreased under T. repens compared with L. perenne. The L. perenne system sequestered more ¹⁵N fertilizer than T. repens: 179 vs. 101 kg N ha^?1 for the low rate of N fertilization and 393 vs. 319 kg N ha^?1 for the high N‐fertilization rate. As the loss of fertilizer‐¹⁵N contributed to the ¹⁵N‐isotope dilution under T. repens, the input of fixed N into the soil could not be estimated. Although N₂ fixation was an important source of N in the T. repens system, there was no significant increase in total soil C compared with a non‐N₂‐fixing L. perenne system. This suggests that N₂ fixation and the availability of N are not the main factors controlling soil C sequestration in a T. repens system.