Nitrous oxide emissions from inland waters: Are IPCC estimates too high?

Nitrous oxide (N₂O) emissions from inland waters remain a major source of uncertainty in global greenhouse gas budgets. N₂O emissions are typically estimated using emission factors (EFs), defined as the proportion of the terrestrial nitrogen (N) load to a water body that is emitted as N₂O to the atmosphere. The Intergovernmental Panel on Climate Change (IPCC) has proposed EFs of 0.25% and 0.75%, though studies have suggested that both these values are either too high or too low. In this work, we develop a mechanistic modeling approach to explicitly predict N₂O production and emissions via nitrification and denitrification in rivers, reservoirs and estuaries. In particular, we introduce a water residence time dependence, which kinetically limits the extent of denitrification and nitrification in water bodies. We revise existing spatially explicit estimates of N loads to inland waters to predict both lumped watershed and half‐degree grid cell emissions and EFs worldwide, as well as the proportions of these emissions that originate from denitrification and nitrification. We estimate global inland water N₂O emissions of 10.6–19.8 Gmol N year^?1 (148–277 Gg N year^?1), with reservoirs producing most N₂O per unit area. Our results indicate that IPCC EFs are likely overestimated by up to an order of magnitude, and that achieving the magnitude of the IPCC's EFs is kinetically improbable in most river systems. Denitrification represents the major pathway of N₂O production in river systems, whereas nitrification dominates production in reservoirs and estuaries.     

Impacts of monoculture cropland to alley cropping agroforestry conversion on soil N2O emissions

Monoculture croplands are a major source of global anthropogenic emissions of nitrous oxide (N₂O), a potent greenhouse gas that contributes to ozone depletion. Agroforestry has the potential to reduce N₂O emissions. Presently, there is no systematic comparison of soil N₂O emissions between cropland agroforestry and monoculture systems in Central Europe. We investigated the effects of converting the monoculture cropland system into the alley cropping agroforestry system on soil N₂O fluxes at three sites (each site has paired agroforestry and monoculture) in Germany, where agroforestry combined crop rows and poplar short-rotation coppice (SRC). We measured soil N₂O fluxes monthly over 2 years (March 2018–January 2020) using static vented chambers. Annual soil N₂O emissions from agroforestry ranged from 0.21 to 2.73 kg N ha⁻¹ year⁻¹, whereas monoculture N₂O emissions ranged from 0.34 to 3.00 kg N ha⁻¹ year⁻¹. During the rotation of corn crop, with high fertilization rates, agroforestry reduced soil N₂O emissions by 9% to 56% compared to monocultures. This was mainly caused by low soil N₂O emissions from the unfertilized agroforestry tree rows. Soil N₂O fluxes were predominantly controlled by soil mineral N in both agroforestry and monoculture systems. Our findings suggest that optimized fertilizer input will further enhance the potential of agroforestry for mitigating N₂O emissions.     

Global soil nitrous oxide emissions since the preindustrial era estimated by an ensemble of terrestrial biosphere models: Magnitude,attribution, and uncertainty

Our understanding and quantification of global soil nitrous oxide (N₂O) emissions and the underlying processes remain largely uncertain. Here, we assessed the effects of multiple anthropogenic and natural factors, including nitrogen fertilizer (N) application, atmospheric N deposition, manure N application, land cover change, climate change, and rising atmospheric CO₂ concentration, on global soil N₂O emissions for the period 1861–2016 using a standard simulation protocol with seven process‐based terrestrial biosphere models. Results suggest global soil N₂O emissions have increased from 6.3 ± 1.1 Tg N₂O‐N/year in the preindustrial period (the 1860s) to 10.0 ± 2.0 Tg N₂O‐N/year in the recent decade (2007–2016). Cropland soil emissions increased from 0.3 Tg N₂O‐N/year to 3.3 Tg N₂O‐N/year over the same period, accounting for 82% of the total increase. Regionally, China, South Asia, and Southeast Asia underwent rapid increases in cropland N₂O emissions since the 1970s. However, US cropland N₂O emissions had been relatively flat in magnitude since the 1980s, and EU cropland N₂O emissions appear to have decreased by 14%. Soil N₂O emissions from predominantly natural ecosystems accounted for 67% of the global soil emissions in the recent decade but showed only a relatively small increase of 0.7 ± 0.5 Tg N₂O‐N/year (11%) since the 1860s. In the recent decade, N fertilizer application, N deposition, manure N application, and climate change contributed 54%, 26%, 15%, and 24%, respectively, to the total increase. Rising atmospheric CO₂ concentration reduced soil N₂O emissions by 10% through the enhanced plant N uptake, while land cover change played a minor role. Our estimation here does not account for indirect emissions from soils and the directed emissions from excreta of grazing livestock. To address uncertainties in estimating regional and global soil N₂O emissions, this study recommends several critical strategies for improving the process‐based simulations.     

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.     

Fluxes of greenhouse gases from Andosols under coffee in monoculture or shaded by <Emphasis Type="Italic">Inga densiflora</Emphasis> in Costa Rica

The objective of this study was to evaluate the effect of N fertilization and the presence of N₂ fixing leguminous trees on soil fluxes of greenhouse gases. For a one year period, we measured soil fluxes of nitrous oxide (N₂O), carbon dioxide (CO₂) and methane (CH₄), related soil parameters (temperature, water-filled pore space, mineral nitrogen content, N mineralization potential) and litterfall in two highly fertilized (250 kg N ha⁻¹ year⁻¹) coffee cultivation: a monoculture (CM) and a culture shaded by the N₂ fixing legume species Inga densiflora (CIn). Nitrogen fertilizer addition significantly influenced N₂O emissions with 84% of the annual N₂O emitted during the post fertilization periods, and temporarily increased soil respiration and decreased CH₄ uptakes. The higher annual N₂O emissions from the shaded plantation (5.8 ± 0.3 kg N ha⁻¹ year⁻¹) when compared to that from the monoculture (4.3 ± 0.1 kg N ha⁻¹ year⁻¹) was related to the higher N input through litterfall (246 ± 16 kg N ha⁻¹ year⁻¹) and higher potential soil N mineralization rate (3.7 ± 0.2 mg N kg⁻¹ d.w. d⁻¹) in the shaded cultivation when compared to the monoculture (153 ± 6.8 kg N ha⁻¹ year⁻¹ and 2.2 ± 0.2 mg N kg⁻¹ d.w. d⁻¹). This confirms that the presence of N₂ fixing shade trees can increase N₂O emissions. Annual CO₂ and CH₄ fluxes of both systems were similar (8.4 ± 2.6 and 7.5 ± 2.3 t C-CO₂ ha⁻¹ year⁻¹, −1.1 ± 1.5 and 3.3 ± 1.1 kg C-CH₄ ha⁻¹ year⁻¹, respectively in the CIn and CM plantations) but, unexpectedly increased during the dry season.     

Greenhouse gas fluxes over managed grasslands in Central Europe

Central European grasslands are characterized by a wide range of different management practices in close geographical proximity. Site‐specific management strategies strongly affect the biosphere–atmosphere exchange of the three greenhouse gases (GHG) carbon dioxide (CO₂), nitrous oxide (N₂O), and methane (CH₄). The evaluation of environmental impacts at site level is challenging, because most in situ measurements focus on the quantification of CO₂ exchange, while long‐term N₂O and CH₄ flux measurements at ecosystem scale remain scarce. Here, we synthesized ecosystem CO₂, N₂O, and CH₄ fluxes from 14 managed grassland sites, quantified by eddy covariance or chamber techniques. We found that grasslands were on average a CO₂ sink (−1,783 to −91 g CO₂ m⁻² year⁻¹), but a N₂O source (18–638 g CO₂‐eq. m⁻² year⁻¹), and either a CH₄ sink or source (−9 to 488 g CO₂‐eq. m⁻² year⁻¹). The net GHG balance (NGB) of nine sites where measurements of all three GHGs were available was found between −2,761 and −58 g CO₂‐eq. m⁻² year⁻¹, with N₂O and CH₄ emissions offsetting concurrent CO₂ uptake by on average 21 ± 6% across sites. The only positive NGB was found for one site during a restoration year with ploughing. The predictive power of soil parameters for N₂O and CH₄ fluxes was generally low and varied considerably within years. However, after site‐specific data normalization, we identified environmental conditions that indicated enhanced GHG source/sink activity (“sweet spots”) and gave a good prediction of normalized overall fluxes across sites. The application of animal slurry to grasslands increased N₂O and CH₄ emissions. The N₂O‐N emission factor across sites was 1.8 ± 0.5%, but varied considerably at site level among the years (0.1%–8.6%). Although grassland management led to increased N₂O and CH₄ emissions, the CO₂ sink strength was generally the most dominant component of the annual GHG budget.     

Soil GHG fluxes are altered by N deposition: New data indicate lower N stimulation of the N2O flux and greater stimulation of the calculated C pools

The effects of nitrogen (N) deposition on soil organic carbon (C) and greenhouse gas (GHG) emissions in terrestrial ecosystems are the main drivers affecting GHG budgets under global climate change. Although many studies have been conducted on this topic, we still have little understanding of how N deposition affects soil C pools and GHG budgets at the global scale. We synthesized a comprehensive dataset of 275 sites from multiple terrestrial ecosystems around the world and quantified the responses of the global soil C pool and GHG fluxes induced by N enrichment. The results showed that the soil organic C concentration and the soil CO₂, CH₄ and N₂O emissions increased by an average of 3.7%, 0.3%, 24.3% and 91.3% under N enrichment, respectively, and that the soil CH₄ uptake decreased by 6.0%. Furthermore, the percentage increase in N₂O emissions (91.3%) was two times lower than that (215%) reported by Liu and Greaver (Ecology Letters, 2009, 12:1103–1117). There was also greater stimulation of soil C pools (15.70 kg C ha^?1 year^?1 per kg N ha^?1 year^?1) than previously reported under N deposition globally. The global N deposition results showed that croplands were the largest GHG sources (calculated as CO₂ equivalents), followed by wetlands. However, forests and grasslands were two important GHG sinks. Globally, N deposition increased the terrestrial soil C sink by 6.34 Pg CO₂/year. It also increased net soil GHG emissions by 10.20 Pg CO₂‐Geq (CO₂ equivalents)/year. Therefore, N deposition not only increased the size of the soil C pool but also increased global GHG emissions, as calculated by the global warming potential approach.     

Dominance of bacterial ammonium oxidizers and fungal denitrifiers in the complex nitrogen cycle pathways related to nitrous oxide emission

Organic compounds and mineral nitrogen (N) usually increase nitrous oxide (N₂O) emissions. Vinasse, a by‐product of bio‐ethanol production that is rich in carbon, nitrogen, and potassium, is recycled in sugarcane fields as a bio‐fertilizer. Vinasse can contribute significantly to N₂O emissions when applied with N in sugarcane plantations, a common practice. However, the biological processes involved in N₂O emissions under this management practice are unknown. This study investigated the roles of nitrification and denitrification in N₂O emissions from straw‐covered soils amended with different vinasses (CV: concentrated and V: nonconcentrated) before or at the same time as mineral fertilizers at different time points of the sugarcane cycle in two seasons. N₂O emissions were evaluated for 90 days, the period that occurs most of the N₂O emission from fertilizers; the microbial genes encoding enzymes involved in N₂O production (archaeal and bacterial amoA, fungal and bacterial nirK, and bacterial nirS and nosZ), total bacteria, and total fungi were quantified by real‐time PCR. The application of CV and V in conjunction with mineral N resulted in higher N₂O emissions than the application of N fertilizer alone. The strategy of vinasse application 30 days before mineral N reduced N₂O emissions by 65% for CV, but not for V. Independent of rainy or dry season, the microbial processes were nitrification by ammonia‐oxidizing bacteria (AOB) and archaea and denitrification by bacteria and fungi. The contributions of each process differed and depended on soil moisture, soil pH, and N sources. We concluded that amoA‐AOB was the most important gene related to N₂O emissions, which indicates that nitrification by AOB is the main microbial‐driven process linked to N₂O emissions in tropical soil. Interestingly, fungal nirK was also significantly correlated with N₂O emissions, suggesting that denitrification by fungi contributes to N₂O emission in soils receiving straw and vinasse application.     

DMPP reduced nitrification,but not annual N2O emissions from mineral fertilizer applied to oilseed rape on a sandy loam soil

Direct field emissions of nitrous oxide (N₂O) may determine whether biodiesel from oilseed rape (Brassica napus L.) fulfills the EU requirement of at least 50% reduction of greenhouse gas emissions as compared to fossil diesel. However, only few studies have documented fertilizer N emission factors (EF) and mitigation options for N₂O emissions from oilseed rape cropping systems. We conducted a field experiment with three N levels (0, 171, and 217 kg/ha), where the N fertilizer was applied as ammonium sulfate nitrate with or without the nitrification inhibitor 3,4‐dimethylpyrazole phosphate (DMPP). N₂O fluxes were measured using static chambers technique and soil samples were analyzed for water and mineral N content during a monitoring period of 368 days. The DMPP treatments showed a significantly increased level of ammonium () for up to 18 weeks after spring fertilization as compared to the treatments without DMPP. However, this difference did not result in a corresponding decrease in soil content, and no differences in cumulative N₂O emissions were found between any fertilized treatments with or without DMPP (mean, 1.26 kg N₂O‐N ha^?1 year^?1). More field experiments are needed to clarify whether DMPP‐coated mineral fertilizers could mitigate N₂O emissions under different weather conditions, for example, under conditions where fertilization events concurred with rainfall events increasing water‐filled pore space to the assumed 60% threshold for denitrification. Emission factors for mineral N fertilizer were 0.28%–0.36% with a mean of 0.32% across the fertilized treatments. These data concur with recent European studies suggesting that the EF for mineral N fertilizers in oilseed rape cropping systems may typically be lower than the default IPCC value of 1%. Further studies are needed to consolidate an EF for oilseed rape under temperate conditions, which will be determining for the sustainability of Northern European oilseed rape cultivation for biodiesel.     

Drainage increases CO2 and N2O emissions from tropical peat soils

Tropical peatlands are vital ecosystems that play an important role in global carbon storage and cycles. Current estimates of greenhouse gases from these peatlands are uncertain as emissions vary with environmental conditions. This study provides the first comprehensive analysis of managed and natural tropical peatland GHG fluxes: heterotrophic (i.e. soil respiration without roots), total CO₂ respiration rates, CH₄ and N₂O fluxes. The study documents studies that measure GHG fluxes from the soil (n = 372) from various land uses, groundwater levels and environmental conditions. We found that total soil respiration was larger in managed peat ecosystems (median = 52.3 Mg CO₂ ha^?1 year^?1) than in natural forest (median = 35.9 Mg CO₂ ha^?1 year^?1). Groundwater level had a stronger effect on soil CO₂ emission than land use. Every 100 mm drop of groundwater level caused an increase of 5.1 and 3.7 Mg CO₂ ha^?1 year^?1 for plantation and cropping land use, respectively. Where groundwater is deep (≥0.5 m), heterotrophic respiration constituted 84% of the total emissions. N₂O emissions were significantly larger at deeper groundwater levels, where every drop in 100 mm of groundwater level resulted in an exponential emission increase (exp(0.7) kg N ha^?1 year^?1). Deeper groundwater levels induced high N₂O emissions, which constitute about 15% of total GHG emissions. CH₄ emissions were large where groundwater is shallow; however, they were substantially smaller than other GHG emissions. When compared to temperate and boreal peatland soils, tropical peatlands had, on average, double the CO₂ emissions. Surprisingly, the CO₂ emission rates in tropical peatlands were in the same magnitude as tropical mineral soils. This comprehensive analysis provides a great understanding of the GHG dynamics within tropical peat soils that can be used as a guide for policymakers to create suitable programmes to manage the sustainability of peatlands effectively.     

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.     

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.     

Nitrogen addition,rather than altered precipitation,stimulates nitrous oxide emissions in an alpine steppe

Anthropogenic‐driven global change, including changes in atmospheric nitrogen (N) deposition and precipitation patterns, is dramatically altering N cycling in soil. How long‐term N deposition, precipitation changes, and their interaction influence nitrous oxide (N₂O) emissions remains unknown, especially in the alpine steppes of the Qinghai–Tibetan Plateau (QTP). To fill this knowledge gap, a platform of N addition (10 g m⁻² year⁻¹) and altered precipitation (±50% precipitation) experiments was established in an alpine steppe of the QTP in 2013. Long‐term N addition significantly increased N₂O emissions. However, neither long‐term alterations in precipitation nor the co‐occurrence of N addition and altered precipitation significantly affected N₂O emissions. These unexpected findings indicate that N₂O emissions are particularly susceptible to N deposition in the alpine steppes. Our results further indicated that both biotic and abiotic properties had significant effects on N₂O emissions. N₂O emissions occurred mainly due to nitrification, which was dominated by ammonia‐oxidizing bacteria, rather than ammonia‐oxidizing archaea. Furthermore, the alterations in belowground biomass and soil temperature induced by N addition modulated N₂O emissions. Overall, this study provides pivotal insights to aid the prediction of future responses of N₂O emissions to long‐term N deposition and precipitation changes in alpine ecosystems. The underlying microbial pathway and key predictors of N₂O emissions identified in this study may also be used for future global‐scale model studies.     

Postfire nitrogen balance of Mediterranean shrublands: Direct combustion losses versus gaseous and leaching losses from the postfire soil mineral nitrogen flush

Fire is a major factor controlling global carbon (C) and nitrogen (N) cycling. While direct C and N losses caused by combustion have been comparably well established, important knowledge gaps remain on postfire N losses. Here, we quantified both direct C and N combustion losses as well as postfire gaseous losses (N₂O, NO and N₂) and N leaching after a high‐intensity experimental fire in an old shrubland in central Spain. Combustion losses of C and N were 9.4 Mg C/ha and 129 kg N/ha, respectively, representing 66% and 58% of initial aboveground vegetation and litter stocks. Moreover, fire strongly increased soil mineral N concentrations by several magnitudes to a maximum of 44 kg N/ha 2 months after the fire, with N largely originating from dead soil microbes. Postfire soil emissions increased from 5.4 to 10.1 kg N ha^?1 year^?1 for N₂, from 1.1 to 1.9 kg N ha^?1 year^?1 for NO and from 0.05 to 0.2 kg N ha^?1 year^?1 for N₂O. Maximal leaching losses occurred 2 months after peak soil mineral N concentrations, but remained with 0.1 kg N ha^?1 year^?1 of minor importance for the postfire N mass balance. ¹⁵N stable isotope labelling revealed that 33% of the mineral N produced by fire was incorporated in stable soil N pools, while the remainder was lost. Overall, our work reveals significant postfire N losses dominated by emissions of N₂ that need to be considered when assessing fire effects on ecosystem N cycling and mass balance. We propose indirect N gas emissions factors for the first postfire year, equalling to 7.7% (N₂‐N), 2.7% (NO‐N) and 5.0% (N₂O‐N) of the direct fire combustion losses of the respective N gas species.     

CH4 and N2O emissions from smallholder agricultural systems on tropical peatlands in Southeast Asia

There are limited data for greenhouse gas (GHG) emissions from smallholder agricultural systems in tropical peatlands, with data for non-CO₂ emissions from human-influenced tropical peatlands particularly scarce. The aim of this study was to quantify soil CH₄ and N₂O fluxes from smallholder agricultural systems on tropical peatlands in Southeast Asia and assess their environmental controls. The study was carried out in four regions in Malaysia and Indonesia. CH₄ and N₂O fluxes and environmental parameters were measured in cropland, oil palm plantation, tree plantation and forest. Annual CH₄ emissions (in kg CH₄ ha⁻¹ year⁻¹) were: 70.7 ± 29.5, 2.1 ± 1.2, 2.1 ± 0.6 and 6.2 ± 1.9 at the forest, tree plantation, oil palm and cropland land-use classes, respectively. Annual N₂O emissions (in kg N₂O ha⁻¹ year⁻¹) were: 6.5 ± 2.8, 3.2 ± 1.2, 21.9 ± 11.4 and 33.6 ± 7.3 in the same order as above, respectively. Annual CH₄ emissions were strongly determined by water table depth (WTD) and increased exponentially when annual WTD was above −25 cm. In contrast, annual N₂O emissions were strongly correlated with mean total dissolved nitrogen (TDN) in soil water, following a sigmoidal relationship, up to an apparent threshold of 10 mg N L⁻¹ beyond which TDN seemingly ceased to be limiting for N₂O production. The new emissions data for CH₄ and N₂O presented here should help to develop more robust country level ‘emission factors’ for the quantification of national GHG inventory reporting. The impact of TDN on N₂O emissions suggests that soil nutrient status strongly impacts emissions, and therefore, policies which reduce N-fertilisation inputs might contribute to emissions mitigation from agricultural peat landscapes. However, the most important policy intervention for reducing emissions is one that reduces the conversion of peat swamp forest to agriculture on peatlands in the first place.     

Soil-atmosphere exchange of nitrous oxide and methane in New Zealand terrestrial ecosystems and their mitigation options: a review

The two non-CO₂ greenhouse gases (GHGs) nitrous oxide (N₂O) and methane (CH₄) comprise 54.8% of total New Zealand emissions. Nitrous oxide is mainly generated from mineral N originating from animal dung and urine, applied fertiliser N, biologically fixed N₂, and mineralisation of soil organic N. Even though about 96% of the anthropogenic CH₄ emitted in New Zealand is from ruminant animals (methanogenesis), methane uptake by aerobic soils (methanotrophy) can significantly contribute to the removal of CH₄ from the atmpsphere, as the global estimates confirm. Both the net uptake of CH₄ by soils and N₂O emissions from soils are strongly influenced by changes in land use and land management. Quantitative information on the fluxes of these two non-CO₂ GHGs is required for a range of land-use and land-management ecosystems to determine their contribution to the national emissions inventory, and for assessing the potential of mitigation options. Here we report soil N₂O fluxes and CH₄ uptake for a range of land-use and land-management systems collated from published and unpublished New Zealand studies. Nitrous oxide emissions are highest in dairy-grazed pastures (10–12 kg N₂O–N ha^?1 year^{? 1}), intermediate in sheep-grazed pastures, (4–6 kg N₂O–N ha^?1 year^?1), and lowest in forest, shrubland and ungrazed pasture soils (1–2 kg N₂O–N ha^?1 year^?1). N deposited in the form of animal urine and dung, and N applied as fertiliser, are the principal sources of N₂O production. Generally, N₂O emissions from grazed pasture soils are high when the soil water-filled pore-space is above field capacity, and net CH₄ uptake is low or absent. Although nitrification inhibitors have shown some promise in reducing N₂O emissions from grazed pasture systems, their efficacy as an integral part of farm management has yet to be tested. Methane uptake was highest for a New Zealand Beech forest soil (10–11 kg CH₄ ha^?1 year^?1), intermediate in some pine forest soils (4–6 kg CH₄ ha^?1 year^?1), and lowest in most pasture (<1 kg CH₄ ha^?1 year^?1) and cropped soils (1.5 kg CH₄ ha^?1 year^?1). Afforestation /reforestation of pastures results in increases in soil CH₄ uptake, largely as a result of increases in soil aeration status and changes in the population and activities of methanotrophs. Soil CH₄ uptake is also seasonally dependent, being about two to three times higher in a dry summer and autumn than in a wet winter. There are no practical ways yet available to reduce CH₄ emissions from agricultural systems. The mitigation options to reduce gaseous emissions are discussed and future research needs identified.     

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.     

Biochar application as a tool to decrease soil nitrogen losses (NH3 volatilization,N2O emissions,and N leaching) from croplands: Options and mitigation strength in a global perspective

Biochar application to croplands has been proposed as a potential strategy to decrease losses of soil‐reactive nitrogen (N) to the air and water. However, the extent and spatial variability of biochar function at the global level are still unclear. Using Random Forest regression modelling of machine learning based on data compiled from the literature, we mapped the impacts of different biochar types (derived from wood, straw, or manure), and their interactions with biochar application rates, soil properties, and environmental factors, on soil N losses (NH₃ volatilization, N₂O emissions, and N leaching) and crop productivity. The results show that a suitable distribution of biochar across global croplands (i.e., one application of <40 t ha^?1 wood biochar for poorly buffered soils, such as those characterized by soil pH<5, organic carbon<1%, or clay>30%; and one application of <80 t ha^?1 wood biochar, <40 t ha^?1 straw biochar, or <10 t ha^?1 manure biochar for other soils) could achieve an increase in global crop yields by 222–766 Tg yr^?1 (4%–16% increase), a mitigation of cropland N₂O emissions by 0.19–0.88 Tg N yr^?1 (6%–30% decrease), a decline of cropland N leaching by 3.9–9.2 Tg N yr^?1 (12%–29% decrease), but also a fluctuation of cropland NH₃ volatilization by ?1.9–4.7 Tg N yr^?1 (?12%–31% change). The decreased sum of the three major reactive N losses amount to 1.7–9.4 Tg N yr^?1, which corresponds to 3%–14% of the global cropland total N loss. Biochar generally has a larger potential for decreasing soil N losses but with less benefits to crop production in temperate regions than in tropical regions.     

Contribution of plants to N 2 O emissions in soil-winter wheat ecosystem: pot and field experiments

Outdoor pot and field experiments were conducted to assess the role of growing plants in agricultural ecosystem N₂O emissions. N₂O emissions from plants were quantified as the difference in soil-crop system N₂O emissions before and immediately after cutting plants during the main growth stages in 2001–02 and 2002–03 winter wheat seasons. Emissions of N₂O from plants depended on biomass within the same plant developmental status. Field results indicated that the seasonal contribution of N₂O emissions from plants to ecosystem fluxes averaged 25%, ranging from 10% at wheat tillering to 62% at the heading stage. The fluxes of N₂O emissions from plants varied between 0.3 and 3.9 mg N₂O-N m⁻² day⁻¹ and its seasonal amount was equivalent to 0.23% of plant N released as N₂O. A N₂O emission coefficient (N₂O_E, mg N₂O-N g⁻¹ C day⁻¹), defined as N₂O-N emission in milligrams from per gram carbon of plant dry matter within a day, was represented by a 5-fold variation ranging from 0.021 to 0.004 mg N₂O-N g C⁻¹ day⁻¹. A linear relationship (y=0.4611x+0.0015, r ²=0.9352, p < 0.001) between N₂O_E (y) and plant dark respiration rate (x, mg CO₂-C g C⁻¹ day⁻¹) suggested that in the absence of photosynthesis, some N₂O production in plant N assimilation was associated with plant respiration. Although this study could not show whether N₂O was produced or transferred by winter wheat plants, these results indicated an important role for higher plant in N₂O exchange. Identifying its potential contribution is critical for understanding agricultural ecosystem N₂O sources.