no sp. Assessment of Nitrogen Fluxes to Air and Water from Site Scale to Continental Scale | The aim of this study is to illustrate the importance of farm scale heterogeneity on nitrogen (N) losses in agricultural landscapes. Results are exemplified with a chain of N models calculating farm-N balances and distributing the N-surplus to N-losses (volatilisation, denitrification, leaching) and soil-N accumulation/release in a Danish landscape. Possible non-linearities in upscaling are assessed by comparing average model results based on (i) individual farm level calculations and (ii) averaged inputs at landscape level. Effects of the non-linearities that appear when scaling up from farm to landscape are demonstrated. Especially in relation to ammonia losses the non-linearity between livestock density and N-loss is significant (p > 0.999), with around 20-30% difference compared to a scaling procedure not taking this non-linearity into account. A significant effect of farm type on soil N accumulation (p > 0.95) was also identified and needs to be included when modelling landscape level N-fluxes and greenhouse gas emissions.

As a promising amendment, biochar has excellent characteristics and can be used as a remediation agent for diverse types of soil pollution. Biochar is mostly made from agricultural wastes, forestry wastes, and biosolids (eg, sewage sludge), but not all the biochar has the same performance in the improvement of soil quality. There is a lack of guidelines devoted to the selection of biochar to be used for different types of soil pollution, and this can undermine the remediation efficiency. To shed light on this sensitive issue, this review focus on the following aspects, (i) how feedstocks affect biochar properties, (ii) the effects of biochar on heavy metals and organic pollutants in soil, and (iii) the impact on greenhouse gas emissions from soil. Generally, the biochars produced from crop residue and woody biomass which are composed of lignin, cellulose, and hemicellulose are more suitable for organic pollution remediation and greenhouse gas emission reduction, while biochar with high ash content are more suitable for cationic organic pollutant and heavy metal pollution (manure and sludge, etc.). Additionally, the effect of biochar on soil microorganisms shows that gram-negative bacteria in soil tend to use WB biochar with high lignin content, while biochar from OW (rich in P, K, Mg, and other nutrients) is more able to promote enzyme activity. Finally, our recommendations on feedstocks selection are presented in the form of a flow diagram, which is precisely intended to be used as a support for decisions on the crucial proportioning conditions to be selected for the preparation of biochar having specific properties and to maximize its efficiency in pollution control.

Human activities such as dams disturb the structure and function of wetlands, triggering large soil CO₂ and CH₄ emissions. However, controls over field CO₂ and CH₄ emissions and their carbon isotopic signatures in reservoir wetlands are not yet fully understood. We investigated in situ CO₂ and CH₄ emissions, the δ¹³C values of CO₂ and CH₄, and associated environments in the saturated and drained states under four elevations (i.e., the water column, <147 m, permanent inundation area without plants; the low, 145–160 m, frequently flooded area with revegetation; the high, 160–175 m, rarely flooded area with revegetation; and the upland area as the control, >175 m, nonflooded area with original plants) in the Three Gorges Reservoir area. The CO₂ emissions was significantly higher in high elevation, and they also significantly differed between the saturated and drained states. In contrast, the CH₄ emissions on average (41.97 μg CH₄ m⁻² h⁻¹) were higher at high elevations than at low elevations (22.73 μg CH₄ m⁻² h⁻¹) during the whole observation period. CH₄ emissions decreased by 90% at low elevations and increased by 153% at high elevations from the saturated to drained states. The δ¹³C of CH₄ was more enriched at high elevations than in the low and upland areas, with a more depleted level under the saturated state than under the drained state. We found that soil CO₂ and CH₄ emissions were closely related to soil substrate quality (e.g., C: N ratio) and enzyme activities, whereas the δ¹³C values of CO₂ and CH₄ were primarily associated with root respiration and methanogenic bacteria, respectively. Specifically, the effects of the saturated and drained states on soil CO₂ and CH₄ emissions were stronger than the effect of reservoir elevation, thereby providing an important basis for assessing carbon neutrality in response to anthropogenic activities.

Biochar is often applied to paddy soils as a soil improver, as it retains nutrients and increases C sequestration; as such, it is a tool in the move towards C-neutral agriculture. Nitrogen (N) fertilizers have been excessively applied to rice paddies, particularly in small farms in China, because N is the major limiting factor for rice production. In paddy soils, dynamic changes in iron (Fe) continuously affect soil emissions of methane (CH₄) and carbon dioxide (CO₂); however, the links between Fe dynamics and greenhouse gas emissions, dissolved organic carbon (DOC), and rice yields following application of biochar remain unclear. The aims of this study were to examine the effects of two rates of nitrogen (N)-enriched biochar (4 and 8 t ha⁻¹ y⁻¹) on paddy soil C emissions and storage, rice yields, and Fe dynamics in subtropical early and late rice growing seasons. Field application of N-enriched biochar at 4 and 8 t ha⁻¹ increased C emissions in early and late rice, whereas application at 4 t ha⁻¹ significantly increased rice yields. The results of a culture experiment and a field experiment showed that the application of N-enriched biochar increased soil Fe²⁺concentration. There were positive correlations between Fe²⁺concentrations and soil CO₂, CH₄, and total C emissions, and with soil DOC concentrations. On the other way around, these correlations were negative for soil Fe³⁺concentrations. In the soil culture experiment, under the exclusion of plant growth, N-enriched biochar reduced cumulative soil emissions of CH₄ and CO₂. We conclude that moderate inputs of N-rich biochar (4 t ha⁻¹) increase rice crop yield and biomass, and soil DOC concentrations, while moderating soil cumulative C emissions, in part, by the impacts of biochar on soil Fe dynamics. We suggest that water management strategies, such as dry-wet cycles, should be employed in rice cultivation to increase Fe²⁺ oxidation for the inhibition of soil CH₄ and CO₂ production. Overall, we showed that application of 4 t ha⁻¹ of N-enriched biochar may represent a potential tool to improve sustainable food production and security, while minimizing negative environmental impacts.

The combined application of organic and synthetic nitrogen (N) fertilizers is being widely recommended in China’s vegetable systems to reduce reliance on synthetic N fertilizer. However, the effect of substituting synthetic fertilizer with organic fertilizer on vegetable productivity (yield, N uptake and nitrogen use efficiency) and reactive nitrogen (Nr) losses (N₂O emission, N leaching and NH₃ volatilization) remains unclear. A meta-analysis was performed using peer-reviewed papers published from 2000 to 2019 to comprehensively assess the effects of combined application of organic and synthetic N fertilizers. The results indicate that overall, the vegetable yield, N₂O emission and NH₃ volatilization were not significantly changed, whereas N leaching was reduced by 44.6% and soil organic carbon (SOC) concentration increased by 12.5% compared to synthetic N fertilizer alone. Specifically, when synthetic N substitution rates (SRs) were ≤70%, vegetable yields and SOC concentration were increased by 5.5%–5.6% and 13.1–18.0%, and N leaching was reduced by 41.6%–48.1%. At the high substitution rate (SR>70%), vegetable yield was reduced by 13.6%, N₂O emission was reduced by 14.3%, and SOC concentration increased by 16.4%. Mixed animal-plant sources of organic N preferentially increased vegetable yield and SOC concentration, and reduced N₂O emission and N leaching compared with single sources of organic-N. Greenhouse gas (GHG) emission was decreased by 28.4%–34.9% by combined applications of organic and synthetic N sources, relative to synthetic N fertilizer alone. We conclude that appropriate rates (SR ≤ 70%) of combined applications of organic and synthetic N fertilizers could improve vegetable yields, decrease Nr and GHG emission, and facilitate sustainable development of coupled vegetable-livestock systems.

Supplemental activated biochar pellet fertilizers (ABPFs) were evaluated as a method to sequester carbon and reduce greenhouse gas (GHG) emissions, and improve rice production. The evaluated treatments were a control (standard cultivation method, no additives applied), activated rice hull biochar pellets with 40% of N (ARHBP-40%), and activated palm biochar pellets with 40% of N (APBP-40%). The N supplied by the ARHBP-40% and APBP-40% treatments reduced the need for supplemental inorganic nitrogen (N) fertilizer by 60 percent. The ARHBP-40% treatment sequestered as much as 1.23 tonne ha⁻¹ compared to 0.89 tonne ha⁻¹ in the control during the rice-growing season. In terms of greenhouse gas (GHG) emissions, CH₄ emissions were not significantly different (p > 0.05) between the control and the ARHBP-40%, while the lowest N₂O emissions (0.002 kg ha⁻¹) were observed in the ARHBP-40% during the crop season. Additionally, GHG (CO₂-equiv.) emissions from the ARHBP-40% application were reduced by 10 kg ha⁻¹ compared to the control. Plant height in the control was relatively high compared to others, but grain yield was not significantly different among the treatments. The application of the ARHBP-40% can mitigate greenhouse gas emissions and enhance carbon sequestration in crop fields, and ABPFs can increase N use efficiency and contribute to sustainable agriculture.

The effects of warming and elevated ozone (O₃) concentrations on nitrous oxide (N₂O) emission from cropland has received increasing attention; however, the small number of studies on this topic impedes understanding. A field experiment was performed to explore the role of warming and elevated O₃ concentrations on N₂O emission from wheat-soybean rotation cropland from 2012 to 2013 using open-top chambers (OTCs). Experimental treatments included ambient temperature (control), elevated temperature (+2 °C), elevated O₃ (100 ppb), and combined elevated temperature (+2 °C) and O₃ (100 ppb). Results demonstrate that warming significantly increased the accumulative amount of N₂O (AAN) emitted from the soil-winter wheat system due to enhanced nitrification rates in the wheat farmland and nitrate reductase activity in wheat leaves. However, elevated O₃ concentrations significantly decreased AAN emission from the soil-soybean system owing to reduced nitrification rates in the soybean farmland. The combined treatment of warming and elevated O₃ inhibited the emission of N₂O from the soybean farmland. Additionally, both the warming and combined treatments significantly increased soil nitrification rates in winter wheat and soybean croplands and decreased denitrification rates in the winter wheat cropping system. Our results suggest that global warming and elevated O₃ concentrations will strongly affect N₂O emission from wheat-soybean rotation croplands.

Anaerobic ammonium oxidation (anammox), denitrifying anaerobic methane oxidation bacteria (DAMO) have received great attention for their excellent performance in nitrogen removal. However, not much study focused on the co-existence of anammox, DAMO, and denitrification in constructed wetlands, not to mention the advantage of their application in mitigating the necessary byproduct nitrous oxide (N₂O), methane (CH₄) from the biodegradation process. In this study, the result indicated the construction of integrated vertical constructed wetlands (IVCWs) contributed to the high-efficient stable simultaneous anammox, DAMO and denitrification (SADD) process for the nutrients removal, with denitrification being the least contributor to nitrogen reduction. Besides the succession of SADD process was largely the driver for the variation of N₂O, CH₄ emission. The structural equation method (SEM) further suggested that the three biological pathways of qnorB/bacteria, archaea/qnorB, and anammox/nirK accounted for the N₂O production, as were top-controlled by mcrA/DAMO in IVCWs. Besides the anammox-associated nitrifier denitrification was the main source for N₂O production. And that the trade-off effect between the CH₄ and N₂O production was exerted by the DAMO, while the influence was far from satisfactory under the methane constraints.

Increasing indirect nitrous oxide (N₂O) emission from river networks as a result of enhanced human activities on landscapes has become a global issue, as N₂O has been widely recognized as an important ozone-depleting greenhouse gas. However, indirect N₂O emissions from different rivers, particularly for those that drain completely different landscapes, are poorly understood. Here, we investigated the spatial-temporal variability of N₂O emissions among the different rivers in the Chaohu Lake Basin of Eastern China. Our results showed that river reaches in urban watersheds are the hotspots of N₂O production, with a mean N₂O concentration of ∼410 nmol L⁻¹, which is 9–18 times greater than those mainly draining forested (23 nmol L⁻¹), agricultural (42 nmol L⁻¹) and mixed (45 nmol L⁻¹) landscapes. Riverine dissolved N₂O was generally supersaturated with respect to the atmosphere. Such N₂O saturation can best be explained by nitrogen availability, except for those in the forested watersheds, where dissolved oxygen is thought to be the primary predictor. The estimated N₂O fluxes in urban rivers reached ∼471 μmol m⁻² d⁻¹, a value of ∼22, 13, and 11 times that in forested, agricultural and mixed watersheds, respectively. Averaged riverine N₂O emission factors (EF₅ᵣ) of the forested, agricultural, urban and mixed watersheds were 0.066%, 0.12%, 0.95% and 0.16%, respectively, showing different deviations from the default EF₅ᵣ that released by IPCC in 2019. This points to a need for more field measurements with wider spatial coverage and finer frequency to further refine the EF₅ᵣ and to better reveal the mechanisms behind indirect N₂O emissions as influenced by watershed landscapes.

CH₄ oxidation in landfill cover soils plays a significant role in mitigating CH₄ release to the atmosphere. Oxygen availability and the presence of co-contaminants are potentially important factors affecting CH₄ oxidation rate and the fate of CH₄-derived carbon. In this study, microbial populations that oxidize CH₄ and the subsequent conversion of CH₄-derived carbon into CO₂, soil organic C and biomass C were investigated in landfill cover soils at two O₂ tensions, i.e., O₂ concentrations of 21% (“sufficient”) and 2.5% (“limited”) with and without toluene. CH₄-derived carbon was primarily converted into CO₂ and soil organic C in the landfill cover soils, accounting for more than 80% of CH₄ oxidized. Under the O₂-sufficient condition, 52.9%–59.6% of CH₄-derived carbon was converted into CO₂ (CECO₂₋C), and 29.1%–39.3% was converted into soil organic C (CEₒᵣgₐₙᵢc₋C). A higher CEₒᵣgₐₙᵢc₋C and lower CECO₂₋C occurred in the O₂-limited environment, relative to the O₂-sufficient condition. With the addition of toluene, the carbon conversion efficiency of CH₄ into biomass C and organic C increased slightly, especially in the O₂-limited environment. A more complex microbial network was involved in CH₄ assimilation in the O₂-limited environment than under the O₂-sufficient condition. DNA-based stable isotope probing of the community with ¹³CH₄ revealed that Methylocaldum and Methylosarcina had a higher relative growth rate than other type I methanotrophs in the landfill cover soils, especially at the low O₂ concentration, while Methylosinus was more abundant in the treatment with both the high O₂ concentration and toluene. These results indicated that O₂-limited environments could prompt more CH₄-derived carbon to be deposited into soils in the form of biomass C and organic C, thereby enhancing the contribution of CH₄-derived carbon to soil community biomass and functionality of landfill cover soils (i.e. reduction of CO₂ emission).