Modeling nitrous oxide emission from rivers: a global assessment

Estimates of global riverine nitrous oxide (N₂O) emissions contain great uncertainty. We conducted a meta‐analysis incorporating 169 observations from published literature to estimate global riverine N₂O emission rates and emission factors. Riverine N₂O flux was significantly correlated with NH₄, NO₃ and DIN (NH₄ + NO₃) concentrations, loads and yields. The emission factors EF(a) (i.e., the ratio of N₂O emission rate and DIN load) and EF(b) (i.e., the ratio of N₂O and DIN concentrations) values were comparable and showed negative correlations with nitrogen concentration, load and yield and water discharge, but positive correlations with the dissolved organic carbon : DIN ratio. After individually evaluating 82 potential regression models based on EF(a) or EF(b) for global, temperate zone and subtropical zone datasets, a power function of DIN yield multiplied by watershed area was determined to provide the best fit between modeled and observed riverine N₂O emission rates (EF(a): R² = 0.92 for both global and climatic zone models, n = 70; EF(b): R² = 0.91 for global model and R² = 0.90 for climatic zone models, n = 70). Using recent estimates of DIN loads for 6400 rivers, models estimated global riverine N₂O emission rates of 29.6–35.3 (mean = 32.2) Gg N₂O–N yr⁻¹ and emission factors of 0.16–0.19% (mean = 0.17%). Global riverine N₂O emission rates are forecasted to increase by 35%, 25%, 18% and 3% in 2050 compared to the 2000s under the Millennium Ecosystem Assessment's Global Orchestration, Order from Strength, Technogarden, and Adapting Mosaic scenarios, respectively. Previous studies may overestimate global riverine N₂O emission rates (300–2100 Gg N₂O–N yr⁻¹) because they ignore declining emission factor values with increasing nitrogen levels and channel size, as well as neglect differences in emission factors corresponding to different nitrogen forms. Riverine N₂O emission estimates will be further enhanced through refining emission factor estimates, extending measurements longitudinally along entire river networks and improving estimates of global riverine nitrogen loads.     

A state-of-the-art review on nitrous oxide control from waste treatment and industrial sources

This review aims at holistically analyzing the environmental problems associated with nitrous oxide (N₂O) emissions by evaluating the most important sources of N₂O and its environmental impacts. Emissions from wastewater treatment processes and the industrial production of nitric and adipic acid represent nowadays the most important anthropogenic point sources of N₂O. Therefore, state-of-the-art strategies to mitigate the generation and release to the atmosphere of this greenhouse and O₃-depleting gas in the waste treatment and industrial sectors are also reviewed. An updated review of the end-of-the-pipe technologies for N₂O abatement, both in the waste treatment and industrial sectors, is herein presented and critically discussed for the first time. Despite the consistent efforts recently conducted in the development of cost-efficient and eco-friendly N₂O abatement technologies, physical/chemical technologies still constitute the most popular treatments for the control of industrial N₂O emissions at commercial scale. The recent advances achieved on biological N₂O abatement based on heterotrophic denitrification have opened new opportunities for the development of eco-friendly alternatives for the treatment of N₂O emissions. Finally, the main limitations and challenges faced by these novel N₂O abatement biotechnologies are identified in order to pave the way for market implementation.     

Gross nitrous oxide production drives net nitrous oxide fluxes across a salt marsh landscape

Sea level rise will change inundation regimes in salt marshes, altering redox dynamics that control nitrification – a potential source of the potent greenhouse gas, nitrous oxide (N₂O) – and denitrification, a major nitrogen (N) loss pathway in coastal ecosystems and both a source and sink of N₂O. Measurements of net N₂O fluxes alone yield little insight into the different effects of redox conditions on N₂O production and consumption. We used in situ measurements of gross N₂O fluxes across a salt marsh elevation gradient to determine how soil N₂O emissions in coastal ecosystems may respond to future sea level rise. Soil redox declined as marsh elevation decreased, with lower soil nitrate and higher ferrous iron in the low marsh compared to the mid and high marshes (P < 0.001 for both). In addition, soil oxygen concentrations were lower in the low and mid‐marshes relative to the high marsh (P < 0.001). Net N₂O fluxes differed significantly among marsh zones (P = 0.009), averaging 9.8 ± 5.4 μg N m^?2 h^?1, ?2.2 ± 0.9 μg N m^?2 h^?1, and 0.67 ± 0.57 μg N m^?2 h^?1 in the low, mid, and high marshes, respectively. Both net N₂O release and uptake were observed in the low and high marshes, but the mid‐marsh was consistently a net N₂O sink. Gross N₂O production was highest in the low marsh and lowest in the mid‐marsh (P = 0.02), whereas gross N₂O consumption did not differ among marsh zones. Thus, variability in gross N₂O production rates drove the differences in net N₂O flux among marsh zones. Our results suggest that future studies should focus on elucidating controls on the processes producing, rather than consuming, N₂O in salt marshes to improve our predictions of changes in net N₂O fluxes caused by future sea level rise.     

冻融循环期间土壤氧化亚氮排放影响因素

全球气候变化可能会提高冻融循环时间、强度以及频率, 从而可能显著影响土壤氧化亚氮(N₂O)排放。N₂O是一种重要的温室气体, 但目前对冻融循环期间土壤N₂O排放规律以及影响因素的了解还有限。为此, 该研究采用整合分析方法, 从已发表文献中收集了30篇关于冻融循环对土壤N₂O通量和累积排放量影响的文献, 探究冻融循环在不同生态系统对N₂O排放的影响, 从试验设置、土壤基本理化性质以及冻融循环格局等角度全面综合地探究其排放影响因素。该研究得出, 冻融循环能显著增加N₂O通量、N₂O累积排放量和硝化作用速率, 全球平均增幅分别为72.34%、143.25%和124.63%; 冻融循环也可增加反硝化作用速率, 全球平均增幅为162.56%; 与之相反, 冻融循环显著减少微生物生物量氮含量, 全球平均减幅为6.39%。不同生态系统土壤水热条件和基本理化性质差异可显著影响冻融循环对N₂O排放的影响。当年平均气温超过5 ℃时, 冻融循环作用可显著提高N₂O通量104.13%, 显著高于年平均气温为0-5 ℃ (25.56%)和小于0 ℃ (55.29%)时; 土壤湿度大于70%时, N₂O通量增加109.17%, 显著高于土壤湿度为50%-70% (65.67%)和小于50% (20.37%)时的通量。土壤黏粒和养分含量越高的土壤区域, 冻融循环对N₂O排放的提高幅度越大。在有植物存在时, 冻融循环可显著提高土壤N₂O通量达91.21%, 高于无植物存在时的54.43%。土壤过筛和在冻融循环期间采集土壤都会增加冻融循环对N₂O排放的影响。另外, 融化时间长, 冻结强度大和冻融循环频率高均可显著提高土壤N₂O累积排放量对冻融循环的响应。当冻结温度低于-10 ℃时, 冻融循环对土壤N₂O排放通量的增幅可达100.73%, 显著高于在冻结温度为-10- -5 ℃ (47.74%)和高于-5 ℃ (70.25%)时。主要原因是冻结强度高可促进土壤微生物和土壤结构释放更多的养分, 从而提高N₂O的产生和排放。该研究结果有助于更好地理解土壤N₂O对冻融循环的响应及其影响因素, 为更准确地预测未来全球气候变化对N₂O排放影响提供科学数据支撑。     

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.     

Night and day: short‐term variation in nitrogen chemistry and nitrous oxide emissions from streams

1. Diel variation in metabolism contributes to variation in oxygen (O₂) concentrations in streams. This variation in O₂ and other parameters (e.g. pH) can in turn affect the rates of microbial nitrogen (N) processing, concentrations of nitrogenous solutes and production of the greenhouse gas nitrous oxide (N₂O). We investigated diel variability in emissions of N₂O and the magnitude of short‐term variability in N solutes across 10 streams. 2. Nitrous oxide fluxes varied on average 2.3‐fold over diel cycles. Concentrations would be underestimated by sampling around noon, but N₂O fluxes would not show a consistent bias. Time‐weighted mean daily N₂O flux was strongly related to nitrate concentration (r² = 0.58). Diel patterns in N₂O and dissolved N species were often complex (rather than simple sinusoidal curves), probably reflecting complex underlying processes. 3. Reliance on samples obtained around noon would overestimate daily mean nitrate concentrations by 5% and underestimate ammonium by 32% (average bias across all streams and dates). 4. Dissolved organic N did not show consistent day–night variation. However, the magnitude of diel variability was similar to that observed for dissolved inorganic N. Organic and inorganic N concentrations were often similar. Both appear to be dynamic components of stream N budgets. 5. The Intergovernmental Panel on Climate Change (IPCC) relies upon an emission factor to estimate indirect agricultural N₂O emissions from streams and ground water. The measured emission factor (defined as the ratio of concentrations of N₂O‐N to ‐N) was typically below the recently revised IPCC default figure. Measured values varied on average 1.8‐fold over approximately 24‐h periods and were slightly higher at night than by day. The emission factor was actually highest in streams that were net sinks for N₂O, highlighting a conceptual problem in the current IPCC method. 6. Typical sampling programmes rely on daytime‐only sampling, which might cause bias in results. In our study streams, the bias was generally small. Diel variation in nitrate concentrations was related to mean temperature; variation in ammonium and N₂O concentrations was greatest at low concentrations of nitrite and ammonium.     

Fluxes of nitrous oxide from boreal peatlands as affected by peatland type,water table level and nitrification capacity

Peat soils with high nitrogen content are potential sources of nitrous oxide (N₂O). Fluxes of nitrous oxide were measuredin situ on nine virgin and ten drained peatlands of different hydrology and nutrient status. Numbers of nitrifying bacteria were estimated in different layers of the peat profiles with a most-probable-number technique. Nitrification potentials were determined in soil slurries of pH 4 and 6 from the profiles of six peat soils. Many virgin peatlands showed low N₂O uptake. Lowering of the water table generally increased the average fluxes of N₂O from the soils, although more in minerotrophic (nutrient rich) than in ombrotrophic (nutrient poor) sites. Ammonium oxidizing bacteria were found on only two sites but nitrite oxidizers were detected in almost all peat profiles. More nitrite oxidizers were found in drained than in virgin peat profiles. Nitrification was enhanced after lowering of the water table in minerotrophic peat but not in ombrotrophic peat. The N₂O fluxes correlated positively with the numbers of nitrite oxidizers, nitrification potential, N, P and Ca content and pH of the soil and negatively with the level of water table (expressed as negative values) and K content of the soil.     

Sources and sinks of nitrous oxide (N2O) in deep lakes

As reported from marine systems, we found that also in15 prealpine lakes N₂O concentrations werestrongly correlated with O₂ concentrations. Inoxic waters below the mixed surface layer, N₂Oconcentrations usually increased with decreasingO₂ concentrations. N₂O is produced in oxicepilimnia, in oxic hypolimnia and at oxic-anoxicboundaries, either in the water or at the sediment-waterinterface. It is consumed, however, incompletely anoxic layers. Anoxic water layers weretherefore N₂O undersaturated. All studied lakeswere sources for atmospheric N₂O, including thosewith anoxic, N₂O undersaturated hypolimnia.However, compared to agriculture, lakes seem not tocontribute significantly to atmospheric N₂Oemissions.     

Immediate and long-term nitrogen oxide emissions from tropical forest soils exposed to elevated nitrogen input

Tropical nitrogen (N) deposition is projected to increase substantially within the coming decades. Increases in soil emissions of the climate‐relevant trace gases NO and N₂O are expected, but few studies address this possibility. We used N addition experiments to achieve N‐enriched conditions in contrasting montane and lowland forests and assessed changes in the timing and magnitude of soil N‐oxide emissions. We evaluated transitory effects, which occurred immediately after N addition, and long‐term effects measured at least 6 weeks after N addition. In the montane forest where stem growth was N limited, the first‐time N additions caused rapid increases in soil N‐oxide emissions. During the first 2 years of N addition, annual N‐oxide emissions were five times (transitory effect) and two times (long‐term effect) larger than controls. This contradicts the current assumption that N‐limited tropical montane forests will respond to N additions with only small and delayed increases in soil N‐oxide emissions. We attribute this fast and large response of soil N‐oxide emissions to the presence of an organic layer (a characteristic feature of this forest type) in which nitrification increased substantially following N addition. In the lowland forest where stem growth was neither N nor phosphorus (P) limited, the first‐time N additions caused only gradual and minimal increases in soil N‐oxide emissions. These first N additions were completed at the beginning of the wet season, and low soil water content may have limited nitrification. In contrast, the 9‐ and 10‐year N‐addition plots displayed instantaneous and large soil N‐oxide emissions. Annual N‐oxide emissions under chronic N addition were seven times (transitory effect) and four times (long‐term effect) larger than controls. Seasonal changes in soil water content also caused seasonal changes in soil N‐oxide emissions from the 9‐ and 10‐year N‐addition plots. This suggests that climate change scenarios, where rainfall quantity and seasonality change, will alter the relative importance of soil NO and N₂O emissions from tropical forests exposed to elevated N deposition.     

Estimation of annual nitrous oxide emissions from a transitional grassland-forest region in Saskatchewan, Canada

The increasing atmospheric N₂O concentration and the imbalance in its global budget have triggered the interest in quantifying N₂O fluxes from various ecosystems. This study was conducted to estimate the annual N₂O emissions from a transitional grassland-forest region in Saskatchewan, Canada. The study region was stratified according to soil texture and land use types, and we selected seven landscapes (sites) to cover the range of soil texture and land use characteristics in the region. The study sites were, in turn, stratified into distinguishable spatial sampling units (i.e., footslope and shoulder complexes), which reflected the differences in soils and soil moisture regimes within a landscape. N₂O emission was measured using a sealed chamber method. Our results showed that water-filled pore space (WFPS) was the variable most correlated to N₂O fluxes. With this finding, we estimated the total N₂O emissions by using regression equations that relate WFPS to N₂O emission, and linking these regression equations with a soil moisture model for predicting WFPS. The average annual fluxes from fertilized cropland, pasture/hay land, and forest areas were 2.00, 0.04, and 0.02 kg N₂O-N ha^–1 yr^–1, respectively. The average annual fluxes for the medium- to fine-textured and sandy-textured areas were 1.40 and 0.04 kg N₂O-N ha^–1 yr^–1, respectively. The weighted-average annual flux for the study region is 0.95 kg N₂O-N ha^–1yr^–1. The fertilized cropped areas covered only 47% of the regional area but contributed about 98% of the regional flux. We found that in the clay loam, cropped site, 2% and 3% of the applied fertilizer were emitted as N₂O on the shoulders and footslopes, respectively.Contribution no. R824 of Saskatchewan Center for Soil Research, Saskatoon, Saskatchewan, Canada     

Moderate precipitation reduction enhances nitrogen cycling and soil nitrous oxide emissions in a semi-arid grassland

The ongoing climate change is predicted to induce more weather extremes such as frequent drought and high-intensity precipitation events, causing more severe drying-rewetting cycles in soil. However, it remains largely unknown how these changes will affect soil nitrogen (N)-cycling microbes and the emissions of potent greenhouse gas nitrous oxide (N₂O). Utilizing a field precipitation manipulation in a semi-arid grassland on the Loess Plateau, we examined how precipitation reduction (ca. −30%) influenced soil N₂O and carbon dioxide (CO₂) emissions in field, and in a complementary lab-incubation with simulated drying-rewetting cycles. Results obtained showed that precipitation reduction stimulated plant root turnover and N-cycling processes, enhancing soil N₂O and CO₂ emissions in field, particularly after each rainfall event. Also, high-resolution isotopic analyses revealed that field soil N₂O emissions primarily originated from nitrification process. The incubation experiment further showed that in field soils under precipitation reduction, drying-rewetting stimulated N mineralization and ammonia-oxidizing bacteria in favor of genera Nitrosospira and Nitrosovibrio, increasing nitrification and N₂O emissions. These findings suggest that moderate precipitation reduction, accompanied with changes in drying-rewetting cycles under future precipitation scenarios, may enhance N cycling processes and soil N₂O emissions in semi-arid ecosystems, feeding positively back to the ongoing climate change.     

Methane and nitrous oxide exchange in differently fertilised grassland in southern Germany

We examined the effect of fertilisation (200 kg cattle slurry-N ha^–1 year^–1) on the exchange of N₂O and CH₄ in the soil–plant system of meadow agroecosystems in southern Germany. From 1996 to 1998, we regularly determined the gas fluxes (closed chamber method) and associated environmental parameters. N₂O and CH₄ fluxes were not significantly affected by fertilisation. N₂O fluxes at the unfertilised and fertilised plots were small, generally between 50 and –20 g N m^–2 h^–1. We identified some incidents of N₂O uptake. CH₄-C fluxes ranged from 1.3 to –0.2 mg m^–2 h^–1 and were not significantly different from 0 at both plots. We budgeted an annual net emission of 15.5 and 29.6 mg m^–2 N₂O-N and an annual CH₄-C net emission of 184.2 and 122.7 mg m^–2 at the unfertilised and fertilised plots, respectively. Apparently, rapid N mineralization and uptake in the densely rooted topsoil prevents N losses and the inhibition of CH₄ oxidation.     

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.     

Microbial oxidation of methane,ammonium and carbon monoxide,and turnover of nitrous oxide and nitric oxide in soils

The effect of soil microbial processes on production and/or consumption of atmospheric trace gases was studied in four different soils which were preincubated in the presence of elevated concentrations of CH₄, NH ₄ ⁺ or CO, to simulate the growth of the resident populations of methanotrophic, nitrifying, or carboxydotrophic bacteria, respectively. Oxidation of CH₄, both at atmospheric (1.8 ppmv) and at elevated (3500 ppmv) CH₄ mixing ratios, was stimulated after preincubation with CH₄, but not with NH ₄ ⁺ or CO, indicating that CH₄ was oxidized by methanotrophic, but not by nitrifying or carboxydotrophic bacteria. However, the oxidation of CH₄ was partially inhibited by addition of NH ₄ ⁺ and CO. Analogously, oxidation of NH ₄ ⁺ was partially inhibited by addition of CH₄. Oxidation of CO at elevated mixing ratios (2300 ppmv) was stimulated after preincubation with CO, indicating oxidation by carboxydotrophs, but was also stimulated at a small extent after preincubation with CH₄, suggesting the involvement of methanotrophs. At atmospheric CO mixing ratios (0.13 ppmv), on the other hand, oxidation of CO was stimulated after preincubation with NH ₄ ⁺ , indicating that the activity was due to nitrifiers. NO uptake was stimulated in soils preincubated with CH₄, indicating the involvement of methanotrophs. However, production of N₂O was only stimulated, if CH₄ was added as a substrate. The results indicate that especially the methanotrophic and nitrifying populations in soil not only oxidize their specific substrates, but are also involved in the metabolism of other compounds.     

Hot spots for nitrous oxide emissions found in different types of permafrost peatlands

Recent findings on large nitrous oxide (N₂O) emissions from permafrost peatlands have shown that tundra soils can support high N₂O release, which is on the contrary to what was thought previously. However, field data on this topic have been very limited, and the spatial and temporal extent of the phenomenon has not been known. To address this question, we studied N₂O dynamics in two types of subarctic permafrost peatlands, a peat plateau in Russia and three palsa mires in Finland, including also adjacent upland soils. The peatlands studied have surfaces that are uplifted by frost (palsas and peat plateaus) and partly unvegetated as a result of wind erosion and frost action. Unvegetated peat surfaces with high N₂O emissions were found from all the studied peatlands. Very high N₂O emissions were measured from peat circles at the Russian site (1.40±0.15 g N₂O m^?2 yr^?1). Elevated, sparsely vegetated peat mounds at the same site had significantly lower N₂O release. The N₂O emissions from bare palsa surfaces in Northern Finland were highly variable but reached high rates, similar to those measured from the peat circles. All the vegetated soils studied had negligible N₂O release. At the bare peat surfaces, the large N₂O emissions were supported by the absence of plant N uptake, the low C : N ratio of the peat, the relatively high gross N mineralization rate and favourable moisture content, together increasing availability of mineral N for N₂O production. We hypothesize that frost heave is crucial for high N₂O emissions, since it lifts the peat above the water table, increasing oxygen availability and making it vulnerable to the the physical processes that may remove the vegetation cover. In the future, permafrost thawing may change the distribution of wet and dry surfaces in permafrost peatlands, which will affect N₂O emissions.     

Factors promoting emissions of nitrous oxide and nitric oxide from denitrifying sequencing batch reactors operated with methanol and ethanol as electron donors

The emissions of nitrous oxide (N₂O) and nitric oxide (NO) from biological nitrogen removal (BNR) operations via nitrification and denitrification is gaining increased prominence. While many factors relevant to the operation of denitrifying reactors can influence N₂O and NO emissions from them, the role of different organic carbon sources on these emissions has not been systematically addressed or interpreted. The overall goal of this study was to evaluate the impact of three factors, organic carbon limitation, nitrite concentrations, and dissolved oxygen concentrations on gaseous N₂O and NO emissions from two sequencing batch reactors (SBRs), operated, respectively, with methanol and ethanol as electron donors. During undisturbed ultimate‐state operation, emissions of both N₂O and NO from either reactor were minimal and in the range of <0.2% of influent nitrate‐N load. Subsequently, the two reactors were challenged with transient organic carbon limitation and nitrite pulses, both of which had little impact on N₂O or NO emissions for either electron donor. In contrast, transient exposure to oxygen led to increased production of N₂O (up to 7.1% of influent nitrate‐N load) from ethanol grown cultures, owing to their higher kinetics and potentially lower susceptibility to oxygen inhibition. A similar increase in N₂O production was not observed from methanol grown cultures. These results suggest that for dissolved oxygen, but not for carbon limitation or nitrite exposure, N₂O emission from heterotrophic denitrification reactors can vary as a function of the electron donor used. Biotechnol. Bioeng. 2010; 106: 390–398. © 2010 Wiley Periodicals, Inc.     

Black alder (Alnus Glutinosa (L.) Gaertn.) trees mediate methane and nitrous oxide emission from the soil to the atmosphere

Three-year-old seedlings of black alder (Alnus glutinosa (L.) Gaertn.), a common European wetland tree species, were grown in native soil taken from an alder swamp. Fluxes of methane (CH₄) and nitrous oxide (N₂O) between the tree stem and the atmosphere were determined under controlled conditions. Both CH₄ and N₂O were emitted through the bark of the stem into the atmosphere when the root zone exhibited higher-than-ambient CH₄ and N₂O gas mixing ratios. Flooding of the soil caused a decreased N₂O emission but an increased CH₄ efflux from the stem. Immediately after flooding of the soil, N₂O was emitted from the seedlings' bark at a rate of 350 mol N₂O m^-2 h^-1 whereas CH₄ flux could not be detected. After more than 40 days of flooding CH₄ fluxes up to 3750 mol CH₄ m^-2 h^-1 from the stem were measured, while N₂O emission had decreased below the limit of detection. Gas efflux decreased with increasing stem height and correlated with gas mixing ratios in the soil, indicating diffusion through the aerenchyma as the major path of gas transport. From these results it is assumed that woody species with aerenchyma can serve as conduits for soil-derived trace gases into the atmosphere, to date only shown for herbaceous plants. This, yet unidentified, woody plant pathway contributes to the total greenhouse gas source strength of wetlands.     

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.     

Climate- and crop-responsive emission factors significantly alter estimates of current and future nitrous oxide emissions from fertilizer use

The current Intergovernmental Panel on Climate Change (IPCC) default methodology (tier 1) for calculating nitrous oxide (N₂O) emissions from nitrogen applied to agricultural soils takes no account of either crop type or climatic conditions. As a result, the methodology omits factors that are crucial in determining current emissions, and has no mechanism to assess the potential impact of future climate and land‐use change. Scotland is used as a case study to illustrate the development of a new methodology, which retains the simple structure of the IPCC tier 1 methodology, but incorporates crop‐ and climate‐dependent emission factors (EFs). It also includes a factor to account for the effect of soil compaction because of trampling by grazing animals. These factors are based on recent field studies in Scotland and elsewhere in the UK. Under current conditions, the new methodology produces significantly higher estimates of annual N₂O emissions than the IPCC default methodology, almost entirely because of the increased contribution of grazed pasture. Total emissions from applied fertilizer and N deposited by grazing animals are estimated at 10 662 t N₂O‐N yr^?1 using the newly derived EFs, as opposed to 6 796 t N₂O‐N yr^?1 using the IPCC default EFs. On a spatial basis, emission levels are closer to those calculated using field observations and detailed soil modelling than to estimates made using the IPCC default methodology. This can be illustrated by parts of the western Ayrshire basin, which have previously been calculated to emit 8–9 kg N₂O‐N ha^?1 yr^?1 and are estimated here as 6.25–8.75 kg N₂O‐N ha^?1 yr^?1, while the IPCC default methodology gives a maximum emission level of only 3.75 kg N₂O‐N ha^?1 yr^?1 for the whole area. The new methodology is also applied in conjunction with scenarios for future climate‐ and land‐use patterns, to assess how these emissions may change in the future. The results suggest that by 2080, Scottish N₂O emissions may increase by up to 14%, depending on the climate scenario, if fertilizer and land management practices remain unchanged. Reductions in agricultural land use, however, have the potential to mitigate these increases and, depending on the replacement land use, may even reduce emissions to below current levels.