Soil pH as the chief modifier for regional nitrous oxide emissions: New evidence and implications for global estimates and mitigation

Nitrous oxide (N₂O) is a greenhouse gas that also plays the primary role in stratospheric ozone depletion. The use of nitrogen fertilizers is known as the major reason for atmospheric N₂O increase. Empirical bottom‐up models therefore estimate agricultural N₂O inventories using N loading as the sole predictor, disregarding the regional heterogeneities in soil inherent response to external N loading. Several environmental factors have been found to influence the response in soil N₂O emission to N fertilization, but their interdependence and relative importance have not been addressed properly. Here, we show that soil pH is the chief factor explaining regional disparities in N₂O emission, using a global meta‐analysis of 1,104 field measurements. The emission factor (EF) of N₂O increases significantly (p < .001) with soil pH decrease. The default EF value of 1.0%, according to IPCC (Intergovernmental Panel on Climate Change) for agricultural soils, occurs at soil pH 6.76. Moreover, changes in EF with N fertilization (i.e. ΔEF) is also negatively correlated (p < .001) with soil pH. This indicates that N₂O emission in acidic soils is more sensitive to changing N fertilization than that in alkaline soils. Incorporating our findings into bottom‐up models has significant consequences for regional and global N₂O emission inventories and reconciling them with those from top‐down models. Moreover, our results allow region‐specific development of tailor‐made N₂O mitigation measures in agriculture.     

Nitrous oxide emissions from silage maize fields under different mineral nitrogen fertilizer and slurry applications

Intensive dairy farming systems are a large source of emission of the greenhouse gas nitrous oxide (N₂O), because of high nitrogen (N) application rates to grasslands and silage maize fields. The objective of this study was to compare measured N₂O emissions from two different soils to default N₂O emission factors, and to look at alternative emission factors based on (i) the N uptake in the crop and (ii) the N surplus of the system, i.e., N applied minus N uptake by the crop. Twelve N fertilization regimes were implemented on a sandy soil (typic endoaquoll) and a clay soil (typic endoaquept) in the Netherlands, and N₂O emissions were measured throughout the growing season. Highest cumulative fluxes of 1.92 and 6.81 kg N₂O-N ha^–1 for the sandy soil and clay soil were measured at the highest slurry application rate of 250 kg N ha^–1. Background emissions from unfertilized soils were 0.14 and 1.52 kg N₂O-N ha^–1 for the sandy soil and the clay soil, respectively. Emission factors for the sandy soil averaged 0.08, 0.51 and 0.26% of the N applied via fertilizer, slurry, and combinations of both. For the clay soil, these numbers were 1.18, 1.21 and 1.69%, respectively. Surplus N was linearly related to N₂O emission for both the sandy soil (R²=0.60) and the clay soil (R²=0.40), indicating a possible alternative emission factor. We concluded that, in our study, N₂O emission was not linearly related to N application rates, and varied with type and application rate of fertilizer. Finally, the relatively high emission from the clay soil indicates that background emissions might have to be taken into account in N₂O budgets.     

Weakened growth of cropland‐N2O emissions in China associated with nationwide policy interventions

China has experienced rapid agricultural development over recent decades, accompanied by increased fertilizer consumption in croplands; yet, the trend and drivers of the associated nitrous oxide (N₂O) emissions remain uncertain. The primary sources of this uncertainty are the coarse spatial variation of activity data and the incomplete model representation of N₂O emissions in response to agricultural management. Here, we provide new data‐driven estimates of cropland‐N₂O emissions across China in 1990–2014, compiled using a global cropland‐N₂O flux observation dataset, nationwide survey‐based reconstruction of N‐fertilization and irrigation, and an updated nonlinear model. In addition, we have evaluated the drivers behind changing cropland‐N₂O patterns using an index decomposition analysis approach. We find that China's annual cropland‐N₂O emissions increased on average by 11.2 Gg N/year² (p < .001) from 1990 to 2003, after which emissions plateaued until 2014 (2.8 Gg N/year², p = .02), consistent with the output from an ensemble of process‐based terrestrial biosphere models. The slowdown of the increase in cropland‐N₂O emissions after 2003 was pervasive across two thirds of China's sowing areas. This change was mainly driven by the nationwide reduction in N‐fertilizer applied per area, partially due to the prevalence of nationwide technological adoptions. This reduction has almost offset the N₂O emissions induced by policy‐driven expansion of sowing areas, particularly in the Northeast Plain and the lower Yangtze River Basin. Our results underline the importance of high‐resolution activity data and adoption of nonlinear model of N₂O emission for capturing cropland‐N₂O emission changes. Improving the representation of policy interventions is also recommended for future projections.     

The production and emission of nitrous oxide from headwater streams in the Midwestern United States

The emission of nitrous oxide (N₂O) from streams draining agricultural landscapes is estimated by the Intergovernmental Panel on Climate Change (IPCC) to constitute a globally significant source of this gas to the atmosphere, although there is considerable uncertainty in the magnitude of this source. We measured N₂O emission rates and potential controlling variables in 12 headwater streams draining a predominantly agricultural basin on glacial terrain in southwestern Michigan. The study sites were nearly always supersaturated with N₂O and emission rates ranged from ?8.9 to 266.8 μg N₂O‐N m^?2 h^?1 with an overall mean of 35.2 μg N₂O‐N m^?2 h^?1. Stream water NO₃^? concentrations best‐predicted N₂O emission rates. Although streams and agricultural soils in the basin had similar areal emission rates, emissions from streams were equivalent to 6% of the anthropogenic emissions from soils because of the vastly greater surface area of soils. We found that the default value of the N₂O emission factor for streams and groundwater as defined by the IPCC (EF5‐g) was similar to the value observed in this study lending support to the recent downward revision to EF5‐g. However, the EF5‐g spanned four orders of magnitude across our study sites suggesting that the IPCC's methodology of applying one emission factor to all streams may be inappropriate.     

Nitrous oxide emissions in the Shanghai river network: implications for the effects of urban sewage and IPCC methodology

Global nitrogen (N) enrichment has resulted in increased nitrous oxide (N₂O) emission that greatly contributes to climate change and stratospheric ozone destruction, but little is known about the N₂O emissions from urban river networks receiving anthropogenic N inputs. We examined N₂O saturation and emission in the Shanghai city river network, covering 6300 km², over 27 months. The overall mean saturation and emission from 87 locations was 770% and 1.91 mg N₂O‐N m^?2 d^?1, respectively. Nitrous oxide (N₂O) saturation did not exhibit a clear seasonality, but the temporal pattern was co‐regulated by both water temperature and N loadings. Rivers draining through urban and suburban areas receiving more sewage N inputs had higher N₂O saturation and emission than those in rural areas. Regression analysis indicated that water ammonium (NH₄⁺) and dissolved oxygen (DO) level had great control on N₂O production and were better predictors of N₂O emission in urban watershed. About 0.29 Gg N₂O‐N yr^?1 N₂O was emitted from the Shanghai river network annually, which was about 131% of IPCC's prediction using default emission values. Given the rapid progress of global urbanization, more study efforts, particularly on nitrification and its N₂O yielding, are needed to better quantify the role of urban rivers in global riverine N₂O emission.     

Direct emission of methane and nitrous oxide from switchgrass and corn stover: implications for large-scale biomass storage

Little is known about the contributions of biomass feedstock storage to the net greenhouse gas emissions from cellulosic biofuels. Direct emissions of methane and nitrous oxide during decomposition in storage may contribute substantially to the global warming potential of biofuels. In this study, laboratory-scale bales of switchgrass and corn stover were stored under a range of moisture (13.0–32.9%) and temperature (5–35 °C) conditions and monitored for O₂ consumption and CO₂, CH₄, and N₂O production over 8 weeks. Gas concentrations and emissions rates were highly variable within and between experimental groups. Stover bales produced higher CO₂ concentrations (P = 0.0002) and lower O₂ (P < 0.0001) during storage than switchgrass bales. Methane concentrations (1.8–2100 ppm) were inversely correlated with bale moisture (P < 0.05), with emissions rates ranging from 4.4–914.9 μg kg⁻¹ DM day⁻¹. Nitrous oxide concentrations ranged from 0 to 31 ppm, and emissions from switchgrass bales inversely correlated with temperature and moisture (P < 0.0001). Net global warming potential from each treatment (0–2.4 gCO₂e kg⁻¹ DM) suggests that direct emission of methane and nitrous oxide from aerobically stored feedstocks have a small effect on net global warming potential of cellulosic biofuels.     

Nitrous oxide fluxes over establishing biofuel crops: Characterization of temporal variability using the cross‐wavelet analysis

Emissions of nitrous oxide (N₂O) over croplands are a major source of greenhouse gases to the atmosphere. The precise accounting of sources of N₂O is essential to national and global budgets, as well as the understanding of the spatial and temporal relationships with environmental variables such as rainfall, air and soil temperature, and soil moisture. The objective of this work was to investigate the temporal correlations of N₂O fluxes with soil and air temperatures, as well as soil moisture. N₂O fluxes were measured over four biofuel crops in Central Illinois during their establishment phase. Measurements were carried out from 2009 to 2011 using a trace gas analyzer (TGA) with tunable laser technology. Measurements of concentrations of N₂O and CO₂ were taken at the center of four plots of maize/soybean rotation, miscanthus (Miscanthus × giganteus), switchgrass (Panicum virgatum) and a mixture of native prairie plants. Cumulative fluxes indicate an average emission of nitrogen via N₂O fluxes on the order of 1.5 kg N ha^?1 year^?1, in agreement with chamber measurements previously reported for the site. N₂O fluxes were associated with peaks in soil and air temperature, and soil moisture, particularly during spring and winter thaws. Cross‐wavelet analysis was used to investigate the correlation between N₂O fluxes and those variables. Results indicate that N₂O fluxes and meteorological variables have significant covariance in time scales ranging from 4 to 32 days. In addition, temporal delays of 1–8 days were found in those relationships. Cross‐wavelet patterns were similar when relating N₂O fluxes with soil temperature, air temperature and soil moisture. The temporal patterns of fluxes and environmental variables reported here support the modeling of emissions and highlight the importance of considering the timing of fluxes in relation to trends in meteorological variables.     

Forest streams are important sources for nitrous oxide emissions

Streams and river networks are increasingly recognized as significant sources for the greenhouse gas nitrous oxide (N₂O). N₂O is a transformation product of nitrogenous compounds in soil, sediment and water. Agricultural areas are considered a particular hotspot for emissions because of the large input of nitrogen (N) fertilizers applied on arable land. However, there is little information on N₂O emissions from forest streams although they constitute a major part of the total stream network globally. Here, we compiled N₂O concentration data from low‐order streams (~1,000 observations from 172 stream sites) covering a large geographical gradient in Sweden from the temperate to the boreal zone and representing catchments with various degrees of agriculture and forest coverage. Our results showed that agricultural and forest streams had comparable N₂O concentrations of 1.6 ± 2.1 and 1.3 ± 1.8 µg N/L, respectively (mean ± SD) despite higher total N (TN) concentrations in agricultural streams (1,520 ± 1,640 vs. 780 ± 600 µg N/L). Although clear patterns linking N₂O concentrations and environmental variables were difficult to discern, the percent saturation of N₂O in the streams was positively correlated with stream concentration of TN and negatively correlated with pH. We speculate that the apparent contradiction between lower TN concentration but similar N₂O concentrations in forest streams than in agricultural streams is due to the low pH (<6) in forest soils and streams which affects denitrification and yields higher N₂O emissions. An estimate of the N₂O emission from low‐order streams at the national scale revealed that ~1.8 × 10⁹ g N₂O‐N are emitted annually in Sweden, with forest streams contributing about 80% of the total stream emission. Hence, our results provide evidence that forest streams can act as substantial N₂O sources in the landscape with 800 × 10⁹ g CO₂‐eq emitted annually in Sweden, equivalent to 25% of the total N₂O emissions from the Swedish agricultural sector.     

Urbanization can accelerate climate change by increasing soil N2O emission while reducing CH4 uptake

Urban land-use change has the potential to affect local to global biogeochemical carbon (C) and nitrogen (N) cycles and associated greenhouse gas (GHG) fluxes. We conducted a meta-analysis to (1) assess the effects of urbanization-induced land-use conversion on soil nitrous oxide (N₂O) and methane (CH₄) fluxes, (2) quantify direct N₂O emission factors (EF_d) of fertilized urban soils used, for example, as lawns or forests, and (3) identify the key drivers leading to flux changes associated with urbanization. On average, urbanization increases soil N₂O emissions by 153%, to 3.0 kg N ha⁻¹ year⁻¹, while rates of soil CH₄ uptake are reduced by 50%, to 2.0 kg C ha⁻¹ year⁻¹. The global mean annual N₂O EF_d of fertilized lawns and urban forests is 1.4%, suggesting that urban soils can be regional hotspots of N₂O emissions. On a global basis, conversion of land to urban greenspaces has increased soil N₂O emission by 0.46 Tg N₂O-N year⁻¹ and decreased soil CH₄ uptake by 0.58 Tg CH₄-C year⁻¹. Urbanization driven changes in soil N₂O emission and CH₄ uptake are associated with changes in soil properties (bulk density, pH, total N content, and C/N ratio), increased temperature, and management practices, especially fertilizer use. Overall, our meta-analysis shows that urbanization increases soil N₂O emissions and reduces the role of soils as a sink for atmospheric CH₄. These effects can be mitigated by avoiding soil compaction, reducing fertilization of lawns, and by restoring native ecosystems in urban landscapes.     

Dynamics of nitrous oxide in groundwater at the aquatic–terrestrial interface

Few data are available to validate the Intergovernmental Panel on Climate Change's (IPCC) emission factors for indirect emissions of nitrous oxide (N₂O). In particular the N₂O emissions resulting from nitrogen leaching and the associated groundwater and surface drainage (EF5-g) are particularly poorly characterized. In situ push–pull methods have been used to identify the fate of NO₃⁻ in the groundwater. In this study, we adapted a previously published in situ denitrification push–pull method to examine the fate of ¹⁵N₂O introduced into the subsoil–groundwater matrix. Enriched ¹⁵N₂O was manufactured, added to groundwater via a closed system in the laboratory, and then introduced into the groundwater–subsoil matrix in an upland-marsh transition zone of a salt marsh and a forested alluvial riparian zone. Conservative tracers (SF₆ and Br⁻) and ¹⁵N₂O were injected into the groundwater and left for 1–4 h after which the groundwater was sampled. Added ¹⁵N₂O behaved in a conservative manner at one site while the other site showed variability with some injections showing significant consumption (3–8 μg N₂O-¹⁵N kg⁻¹ soil day⁻¹) of ¹⁵N₂O. Our results show that the fate and dynamics of N₂O in groundwater are complex and variable and that these dynamics should be considered in the development of improved IPCC inventory calculations.     

Soil-Atmosphere Exchange of N<Subscript>2</Subscript>O and NO in Near-Natural Savanna and Agricultural Land in Burkina Faso (W. Africa)

In a combined field and laboratory study in the southwest of Burkina Faso, we quantified soil-atmosphere N₂O and NO exchange. N₂O emissions were measured during two field campaigns throughout the growing seasons 2005 and 2006 at five different experimental sites, that is, a natural savanna site and four agricultural sites planted with sorghum (n = 2), cotton and peanut. The agricultural fields were not irrigated and not fertilized. Although N₂O exchange mostly fluctuated between −2 and 8 μg N₂O–N m⁻² h⁻¹, peak N₂O emissions of 10–35 μg N₂O–N m⁻² h⁻¹ during the second half of June 2005, and up to 150 μg N₂O–N m⁻² h⁻¹ at the onset of the rainy season 2006, were observed at the native savanna site, whereas the effect of the first rain event on N₂O emissions at the crop sites was low or even not detectable. Additionally, a fertilizer experiment was conducted at a sorghum field that was divided into three plots receiving different amounts of N fertilizer (plot A: 140 kg N ha⁻¹; plot B: 52.5 kg N ha⁻¹; plot C: control). During the first 3 weeks after fertilization, only a minor increase in N₂O emissions at the two fertilized plots was detected. After 24 days, however, N₂O emission rates increased exponentially at plot A up to a mean of 80 μg N₂O–N m⁻² h⁻¹, whereas daily mean values at plot B reached only 19 μg N₂O–N m⁻² h⁻¹, whereas N₂O flux rates at plot C remained unchanged. The calculated annual N₂O emission of the nature reserve site amounted to 0.52 kg N₂O–N ha⁻¹ a⁻¹ in 2005 and to 0.67 kg N₂O–N ha⁻¹ a⁻¹ in 2006, whereas the calculated average annual N₂O release of the crop sites was only 0.19 kg N₂O–N ha⁻¹ a⁻¹ and 0.20 kg N₂O–N ha⁻¹ a⁻¹ in 2005 and 2006, respectively. In a laboratory study, potential N₂O and NO formation under different soil moisture regimes were determined. Single wetting of dry soil to medium soil water content with subsequent drying caused the highest increase in N₂O and NO emissions with maximum fluxes occurring 1 day after wetting. The stimulating effect lasted for 3–4 days. A weaker stimulation of N₂O and NO fluxes was detected during daily wetting of soil to medium water content, whereas no significant stimulating effect of single or daily wetting to high soil water content (>67% WHC_max) was observed. This study demonstrates that the impact of land-use change in West African savanna on N trace gas emissions is smaller—with the caveat that there could have been potentially higher N₂O and NO emissions during the initial conversion—than the effect of timing and distribution of rainfall and of the likely increase in nitrogen fertilization in the future.     

Lakes as nitrous oxide sources in the boreal landscape

Estimates of regional and global freshwater N₂O emissions have remained inaccurate due to scarce data and complexity of the multiple processes driving N₂O fluxes the focus predominantly being on summer time measurements from emission hot spots, agricultural streams. Here, we present four‐season data of N₂O concentrations in the water columns of randomly selected boreal lakes covering a large variation in latitude, lake type, area, depth, water chemistry, and land use cover. Nitrate was the key driver for N₂O dynamics, explaining as much as 78% of the variation of the seasonal mean N₂O concentrations across all lakes. Nitrate concentrations varied among seasons being highest in winter and lowest in summer. Of the surface water samples, 71% were oversaturated with N₂O relative to the atmosphere. Largest oversaturation was measured in winter and lowest in summer stressing the importance to include full year N₂O measurements in annual emission estimates. Including winter data resulted in fourfold annual N₂O emission estimates compared to summer only measurements. Nutrient‐rich calcareous and large humic lakes had the highest annual N₂O emissions. Our emission estimates for Finnish and boreal lakes are 0.6 and 29 Gg N₂O‐N/year, respectively. The global warming potential of N₂O from lakes cannot be neglected in the boreal landscape, being 35% of that of diffusive CH₄ emission in Finnish lakes.     

Regionally differentiated estimates of cropland N2O emissions reduce uncertainty in global calculations

Nitrogen (N) additions to cropland soils are the largest source of anthropogenic nitrous oxide (N₂O) emissions and are an important contributor to global greenhouse gas radiative forcing. Progress in understanding controls on N₂O fluxes from soils is demonstrated in increasingly sophisticated emissions estimates with improved spatial and source resolution. These methods build upon ongoing field, laboratory, and modeling advances that are restricted to just a handful of countries. Thus, burgeoning new knowledge is of limited utility for improving N₂O emissions estimates for the rest of the world where prospects for near‐term advances are constrained by the limited breadth of observations and availability of model driver data. Here, we use Bayesian inversion to leverage information from recent national‐level N₂O emission inventories and reduce uncertainty by up to 65% for estimates of regional and global direct cropland N₂O emissions. Our estimates for the proportion of N inputs lost as N₂O vary by a factor of two between regions and depart from existing default emission factors, yet regional emissions estimates based on these factors are consistent with global, regional, and local observations. Improved regional emission factors will enhance national greenhouse gas inventories in information‐poor countries and guide efforts to reduce agricultural N₂O emissions.     

Denitrification and N2O emission from urine-affected grassland soil

Denitrification and N₂O emission rates were measured following two applications of artificial urine (40 g urine-N m^–2) to a perennial rye-grass sward on sandy soil. To distinguish between N₂O emission from denitrification or nitrification, urine was also applied with a nitrification inhibitor (dicyandiamide, DCD). During a 14 day period following each application, the soil was frequently sampled, and incubated with and without acetylene to measure denitrification and N₂O emission rates, respectively.Urine application significantly increased denitrification and N₂O emission rates up to 14 days after application, with rates amounting to 0.9 and 0.6 g N m^–2 day^–1 (9 and 6 kg N ha^–1 day^–1), respectively. When DCD was added to the urine, N₂O emission rates were significantly lower from 3 to 7 days after urine application onwards. Denitrification was the main source of N₂O immediately following each urine application. 14 days after the first application, when soil water contents dropped to 15% (v/v) N₂O mainly derived from nitrification.Total denitrification losses during the 14 day periods were 7 g N m^–2, or 18% of the urine-N applied. Total N₂O emission losses were 6.5 and 3 g N m^–2, or 16% and 8% of the urine-N applied for the two periods. The minimum estimations of denitrification and N₂O emission losses from urine-affected soil were 45 to 55 kg N ha^–1 year^–1, and 20 to 50 kg N ha^–1 year^–1, respectively.     

Nitrous oxide and methane emissions from cryptogamic covers

Cryptogamic covers, which comprise some of the oldest forms of terrestrial life on Earth (Lenton & Huntingford, 2003 ), have recently been found to fix large amounts of nitrogen and carbon dioxide from the atmosphere (Elbert et al., 2012 ). Here we show that they are also greenhouse gas sources with large nitrous oxide (N₂O) and small methane (CH₄) emissions. Whilst N₂O emission rates varied with temperature, humidity, and N deposition, an almost constant ratio with respect to respiratory CO₂ emissions was observed for numerous lichens and bryophytes. We employed this ratio together with respiration data to calculate global and regional N₂O emissions. If our laboratory measurements are typical for lichens and bryophytes living on ground and plant surfaces and scaled on a global basis, we estimate a N₂O source strength of 0.32–0.59 Tg year^?1 for the global N₂O emissions from cryptogamic covers. Thus, our emission estimate might account for 4–9% of the global N₂O budget from natural terrestrial sources. In a wide range of arid and forested regions, cryptogamic covers appear to be the dominant source of N₂O. We suggest that greenhouse gas emissions associated with this source might increase in the course of global change due to higher temperatures and enhanced nitrogen deposition.     

Soil CN ratio as a scalar parameter to predict nitrous oxide emissions

Forested histosols have been found in some cases to be major, and in other cases minor, sources of the greenhouse gas nitrous oxide (N₂O). In order to estimate the total national or global emissions of N₂O from histosols, scaling or mapping parameters that can separate low‐ and high‐emitting sites are needed, and should be included in soil databases. Based on interannual measurements of N₂O emissions from drained forested histosols in Sweden, we found a strong negative relationship between N₂O emissions and soil CN ratios (r²_adj=0.96, mean annual N₂O emission=ae^{(?b CN ratio)}). The same equation could be used to estimate the N₂O emissions from Finnish and German sites based on CN ratios in published data. We envisage that the correlation between N₂O emissions and CN ratios could be used to scale N₂O emissions from histosols determined at sampled sites to national levels. However, at low CN ratios (i.e. below 15–20) other parameters such as climate, pH and groundwater tables increase in importance as regulating factors affecting N₂O emissions.     

Methane and nitrous oxide emissions under no‐till farming in China: a meta‐analysis

No‐till (NT) practices are among promising options toward adaptation and mitigation of climate change. However, the mitigation effectiveness of NT depends not only on its carbon sequestration potential but also on soil‐derived CH₄ and N₂O emissions. A meta‐analysis was conducted, using a dataset involving 136 comparisons from 39 studies in China, to identify site‐specific factors which influence CH₄ emission, CH₄ uptake, and N₂O emission under NT. Comparative treatments involved NT without residue retention (NT0), NT with residue retention (NTR), compared to plow tillage (PT) with residue removed (PT0). Overall, NT0 significantly decreased CH₄ emission by ~30% (P < 0.05) compared to PT0 with an average emission 218.8 kg ha⁻¹ for rice paddies. However, the increase in N₂O emission could partly offset the benefits of the decrease in CH₄ emission under NT compared to PT0. NTR significantly enhanced N₂O emission by 82.1%, 25.5%, and 20.8% (P < 0.05) compared to PT0 for rice paddies, acid soils, and the first 5 years of the experiments, respectively. The results from categorical meta‐analysis indicated that the higher N₂O emission could be mitigated by adopting NT within alkaline soils, for long‐term duration, and with less N fertilization input when compared to PT0. In addition, the natural log (lnR) of response ratio of CH₄ and N₂O emissions under NT correlated positively (enhancing emission) with climate factors (temperature and precipitation) and negatively (reducing emission) with experimental duration, suggesting that avoiding excess soil wetness and using NT for a long term could enhance the benefits of NT. Therefore, a thorough understanding of the conditions favoring greenhouse gas(es) reductions is essential to achieving climate change mitigation and advancing food security in China.     

A test of a field‐based 15N–nitrous oxide pool dilution technique to measure gross N2O production in soil

Soils are both a major source and sink of nitrous oxide (N₂O), but the proportion of soil N₂O production released to the atmosphere (termed the N₂O yield) is poorly constrained due to the difficulty in measuring gross N₂O production. The quantification of gross N₂O fluxes would greatly improve our ability to predict N₂O dynamics across the soil‐atmosphere interface. We report a new approach, the ¹⁵N₂O pool dilution technique, to measure rates of gross N₂O production and consumption under laboratory and field conditions. In the laboratory, gross N₂O production and consumption compared well between the ¹⁵N₂O pool dilution and acetylene inhibition methods whereas the ¹⁵NO₃^? tracer method measured significantly higher rates. In the field, N₂O emissions were not significantly affected by increasing chamber headspace concentrations up to 100 ppb ¹⁵N₂O. The pool dilution model estimates of ¹⁴N₂O and ¹⁵N₂O concentrations as well as net N₂O fluxes fit observed data very well, suggesting that the technique yielded robust estimates of gross N₂O production. Estimated gross N₂O consumption rates were underestimated relative to rates calculated as the difference between gross and net N₂O production rates, possibly due to heterogeneous and/or inadequate tracer diffusion to deeper layers in the soil profile. Gross N₂O production rates were high, averaging 8.4 ± 3.2 mg N m^?2 day^?1, and were most strongly correlated to mineral nitrogen concentrations and denitrifying enzyme activity (R² = 0.73). Gross N₂O production rates varied spatially, with the highest rates in soils with the best drainage and the highest mineral N availability. Estimated and calculated N₂O consumption rates constrained the average N₂O yield from 0.70 to 0.84. Our results demonstrate that the ¹⁵N₂O pool dilution technique can provide well‐constrained estimates of N₂O yields and field rates of gross N₂O production correlated to soil characteristics, improving our understanding of terrestrial N₂O dynamics.     

Denitrification and N2O effluxes in the Bothnian Bay (northern Baltic Sea) river sediments as affected by temperature under different oxygen concentrations

Denitrification rates and nitrous oxide (N₂O) effluxes were measured at different temperatures and for different oxygen concentrations in the sediments of a eutrophied river entering the Bothnian Bay. The experiments were made in a laboratory microcosm with intact sediment samples. ¹⁵N-labelling was used to measure denitrification rates (Dw). The rates were measured at four temperatures (5, 10, 15 and 20°C) and with three oxygen inputs (<0.2, 5, and 10 mg O₂ l⁻¹). The temperature response was highly affected by oxygen concentration. At higher O₂ concentrations (5 and 10 mg O₂ l⁻¹) a saturation over 10°C was observed, whereas the anoxic treatment (<0.2 mg O₂ l⁻¹) showed an exponential increase in the temperature interval with a Q ₁₀ value of 3.1. The result is described with a combined statistical model. In contrast with overall denitrification, the N₂O effluxes from sediments decreased with increasing temperature. The N₂O effluxes had a lower response to oxygen than denitrification rates. The N₂O/N₂ ratio was always below 0.02. Increased temperatures in the future could enhance denitrification rates in boreal river sediments but would not increase the amount of N₂O produced.     

Spatial Variation in Denitrification and N2O Emission in Relation to Nitrate Removal Efficiency in a N-stressed Riparian Buffer Zone

Spatial variability in hydrological flowpaths and nitrate-removal processes complicates the overall assessment of riparian buffer zone functioning in terms of water quality improvement as well as enhancement of the greenhouse effect by N₂O emissions. In this study, we evaluated denitrification and nitrous oxide emission in winter and summer along two groundwater flowpaths in a nitrate-loaded forested riparian buffer zone and related the variability in these processes to controlling soil factors. Denitrification and emissions of N₂O were measured using flux chambers and incubation experiments. In winter, N₂O emissions were significantly higher (12.4 mg N m⁻² d⁻¹) along the flowpath with high nitrate removal compared with the flowpath with low nitrate removal (2.58 mg N m⁻² d⁻¹). In summer a reverse pattern was observed, with higher N₂O emissions (13.6 mg N m⁻² d⁻¹) from the flowpath with low nitrate-removal efficiencies. Distinct spatial patterns of denitrification and N₂O emission were observed along the high nitrate-removal transect compared to no clear pattern along the low nitrate-removal transect, where denitrification activity was very low. Results from this study indicate that spots with high nitrate-removal efficiency also contribute significantly to an increased N₂O emission from riparian zones. Furthermore, we conclude that high variability in N₂O:N₂ ratio and weak relationships with environmental conditions limit the value of this ratio as a proxy to evaluate the environmental consequences of riparian buffer zones.