Net greenhouse gas balance in response to nitrogen enrichment: perspectives from a coupled biogeochemical model

Increasing reactive nitrogen (N) input has been recognized as one of the important factors influencing climate system through affecting the uptake and emission of greenhouse gases (GHG). However, the magnitude and spatiotemporal variations of N‐induced GHG fluxes at regional and global scales remain far from certain. Here we selected China as an example, and used a coupled biogeochemical model in conjunction with spatially explicit data sets (including climate, atmospheric CO₂, O₃, N deposition, land use, and land cover changes, and N fertilizer application) to simulate the concurrent impacts of increasing atmospheric and fertilized N inputs on balance of three major GHGs (CO₂, CH₄, and N₂O). Our simulations showed that these two N enrichment sources in China decreased global warming potential (GWP) through stimulating CO₂ sink and suppressing CH₄ emission. However, direct N₂O emission was estimated to offset 39% of N‐induced carbon (C) benefit, with a net GWP of three GHGs averaging ?376.3 ± 146.4 Tg CO₂ eq yr^?1 (the standard deviation is interannual variability of GWP) during 2000–2008. The chemical N fertilizer uses were estimated to increase GWP by 45.6 ± 34.3 Tg CO₂ eq yr^?1 in the same period, and C sink was offset by 136%. The largest C sink offset ratio due to increasing N input was found in Southeast and Central mainland of China, where rapid industrial development and intensively managed crop system are located. Although exposed to the rapidly increasing N deposition, most of the natural vegetation covers were still showing decreasing GWP. However, due to extensive overuse of N fertilizer, China's cropland was found to show the least negative GWP, or even positive GWP in recent decade. From both scientific and policy perspectives, it is essential to incorporate multiple GHGs into a coupled biogeochemical framework for fully assessing N impacts on climate changes.     

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.     

Nitrogen-Use Efficiency,Nitrous Oxide Emissions,and Cereal Production in Brazil: Current Trends and Forecasts

The agriculture sector has historically been a major source of greenhouse gas (GHG) emissions into the atmosphere. Although the use of synthetic fertilizers is one of the most common widespread agricultural practices, over-fertilization can lead to negative economic and environmental consequences, such as high production costs, depletion of energy resources, and increased GHG emissions. Here, we provide an analysis to understand the evolution of cereal production and consumption of nitrogen (N) fertilizers in Brazil and to correlate N use efficiency (NUE) with economic and environmental losses as N₂O emissions. Our results show that the increased consumption of N fertilizers is associated with a large decrease in NUE in recent years. The CO₂ eq. of N₂O emissions originating from N fertilization for cereal production were approximately 12 times higher in 2011 than in 1970, indicating that the inefficient use of N fertilizers is directly related to environmental losses. The projected N fertilizer forecasts are 2.09 and 2.37 million ton for 2015 and 2023, respectively. An increase of 0.02% per year in the projected NUE was predicted for the same time period. However, decreases in the projected CO₂ eq. emissions for future years were not predicted. In a hypothetical scenario, a 2.39% increase in cereal NUE would lead to $ 21 million savings in N fertilizer costs. Thus, increases in NUE rates would lead not only to agronomic and environmental benefits but also to economic improvement.     

N<Subscript>2</Subscript>O and CH<Subscript>4</Subscript> emission from <Emphasis Type="Italic">Miscanthus</Emphasis> energy crop fields in the infertile Loess Plateau of China

Background

The greenhouse gas (GHG) mitigation is one of the most important environmental benefits of using bioenergy replacing fossil fuels. Nitrous oxide (N₂O) and methane (CH₄) are important GHGs and have drawn extra attention for their roles in global warming. Although there have been many works of soil emissions of N₂O and CH₄ from bioenergy crops in the field scale, GHG emissions in large area of marginal lands are rather sparse and how soil temperature and moisture affect the emission potential remains unknown. Therefore, we sought to estimate the regional GHG emission based on N₂O and CH₄ releases from the energy crop fields.

Results

Here we sampled the top soils from two Miscanthus fields and incubated them using a short-term laboratory microcosm approach under different conditions of typical soil temperatures and moistures. Based on the emission measurements of N₂O and CH₄, we developed a model to estimate annual regional GHG emission of Miscanthus production in the infertile Loess Plateau of China. The results showed that the N₂O emission potential was 0.27 kg N ha^?1 year^?1 and clearly lower than that of croplands and grasslands. The CH₄ uptake potential was 1.06 kg C ha^?1 year^?1 and was slightly higher than that of croplands. Integrated with our previous study on the emission of CO₂, the net greenhouse effect of three major GHGs (N₂O, CH₄ and CO₂) from Miscanthus fields was 4.08 t CO_2eq ha^?1 year^?1 in the Loess Plateau, which was lower than that of croplands, grasslands and shrub lands.

Conclusions

Our study revealed that Miscanthus production may hold a great potential for GHG mitigation in the vast infertile land in the Loess Plateau of China and could contribute to the sustainable energy utilization and have positive environmental impact on the region.

     

Woody biochar's greenhouse gas mitigation potential across fertilized and unfertilized agricultural soils and soil moisture regimes

Biochar has been widely researched as an important technology for climate smart agriculture, yet work is still necessary to identify the magnitude of potential greenhouse gas (GHG) mitigation and mechanisms involved. This study measured slow‐pyrolysis wood‐derived biochar's impact on GHG efflux, mineral N dynamics, and soil organic C in a series of two incubations across fertilized and unfertilized agricultural soils and soil moisture regimes. This research explored the magnitude of biochar's full GHG mitigation potential and drivers of such impacts. Results of this incubation indicate slow‐pyrolysis wood‐derived biochar has potential to provide annual emission reductions of 0.58–1.72 Mg CO₂‐eq ha^?1 at a 25 Mg ha^?1 biochar application rate. The greatest GHG mitigation potential was from C sequestration and nitrous oxide (N₂O) reduction in mineral N fertilized soils, with minimal impacts on N₂O emissions in unfertilized soils, carbon dioxide (CO₂) emissions, and methane (CH₄) uptake. Analysis of mineral N dynamics in the bulk soil and on biochar isolates indicated that neither biochar impacts on net mineralization and nitrification nor retention of ammonium () on biochar isolates could explain biochar's N₂O reduction. Instead, biochar amendments exhibited consistent N₂O emission reductions relative to the N₂O emission in the control soil regardless of soil type and fertilization. Results across a soil moisture gradient suggest that woody biochar may aerate soils shifting redox conditions and subsequent N₂O production. Understanding the magnitude of biochar's GHG reduction potential and the mechanisms driving these effects can help inform biochar modeling efforts, explain field results and identify agricultural applications that maximize biochar's full GHG mitigation potential.     

CO2 uptake is offset by CH4 and N2O emissions in a poplar short‐rotation coppice

The need for renewable energy sources will lead to a considerable expansion in the planting of dedicated fast‐growing biomass crops across Europe. These are commonly cultivated as short‐rotation coppice (SRC), and currently poplar (Populus spp.) is the most widely planted. In this study, we report the greenhouse gas (GHG) fluxes of carbon dioxide (CO₂), methane (CH₄) and nitrous oxide (N₂O) measured using eddy covariance technique in an SRC plantation for bioenergy production. Measurements were made during the period 2010–2013, that is, during the first two rotations of the SRC. The overall GHG balance of the 4 years of the study was an emission of 1.90 (±1.37) Mg CO₂eq ha^?1; this indicated that soil trace gas emissions offset the CO₂ uptake by the plantation. CH₄ and N₂O contributed almost equally to offset the CO₂ uptake of ?5.28 (±0.67) Mg CO₂eq ha^?1 with an overall emission of 3.56 (±0.35) Mg CO₂eq ha^?1 of N₂O and of 3.53 (±0.85) Mg CO₂eq ha^?1 of CH₄. N₂O emissions mostly occurred during one single peak a few months after the site was converted to SRC; this peak comprised 44% of the total N₂O loss during the two rotations. Accurately capturing emission events proved to be critical for deriving correct estimates of the GHG balance. The nitrogen (N) content of the soil and the water table depth were the two drivers that best explained the variability in N₂O and CH_4, respectively. This study underlines the importance of the ‘non‐CO₂ GHGs’ on the overall balance. Further long‐term investigations of soil trace gas emissions should monitor the N content and the mineralization rate of the soil, as well as the microbial community, as drivers of the trace gas emissions.     

Effect of improved nitrogen management on greenhouse gas emissions from intensive dairy systems in the Netherlands

Dairy systems in Europe contribute to the emissions of the greenhouse gases (GHGs) nitrous oxide (N₂O), methane (CH₄) and carbon dioxide (CO₂). In this paper, the effects of improved nitrogen (N) management on GHG emissions from Dutch dairy farms are determined. The GHG emissions are calculated using the panel on climate change (IPCC) methodology for the Netherlands, an updated and refined IPCC methodology, and a full accounting approach. The changes in dairy farming over the last 20 years, and the consequences for N management are described using detailed farm‐level data, collected in 1985, 1997 and 2002. The selected years represent distinct stages in the implementation of N policies. The changes in N management have reduced the GHG emissions. A reduction of the N surplus per kilogram milk with 1 g N reduced the GHG emissions per kilogram milk with approximately 29 g CO₂‐equivalents. The reduction of the N surpluses was mainly brought about by reduced fertilizer use and reduced grazing time. The use of updated and refined emission factors resulted in higher CH₄ emissions and lower N₂O emissions. On average, the overall emission was 36% higher with the refined method. Full accounting, including all direct and indirect emissions of CH₄, N₂O and CO₂, increased the emission with 36% compared with the refined IPCC methodology. We conclude that the N surplus at farm level is a useful indicator of GHG emissions. A full accounting system as presented in this study may effectively enable farmers to address the issue of emissions of GHGs in their operational management decisions. Both approaches serve their own specific objectives: full accounting at the farm level to explore mitigation options, and the IPCC methods to report changes in GHG emissions at the national level.     

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.     

Bioethanol production from sugarcane and emissions of greenhouse gases – known and unknowns

Bioethanol production from sugarcane is discussed as an alternative energy source to reduce dependencies of regional economies on fossil fuels. Even though bioethanol production from sugarcane is considered to be a beneficial and cost‐effective greenhouse gas (GHG) mitigation strategy, it is still a matter of controversy due to insufficient information on the total GHG balance of this system. Aside from the necessity to account for the impact of land use change (LUC), soil N₂O emissions during sugarcane production and emissions of GHG due to preharvest burning may significantly impact the GHG balance. Based on a thorough literature review, we show that direct N₂O emissions from sugarcane fields due to nitrogen (N) fertilization result in an emission factor of 3.87±1.16% which is much higher than suggested by IPCC (1%). N₂O emissions from N fertilization accounted for 40% of the total GHG emissions from ethanol–sugarcane production, with an additional 17% from trash burning. If LUC‐related GHG emissions are considered, the total GHG balance turns negative mainly due to vegetation carbon losses. Our study also shows that major gaps in knowledge still exist about GHG sources related to agricultural management during sugarcane production, e.g. effects of irrigation, vinasse and filter cake application. Therefore, more studies are needed to assess if bioethanol from sugarcane is a viable option to reduce energy‐related GHG emissions.     

Estimation of nitrous oxide, nitric oxide and ammonia emissions from croplands in East, Southeast and South Asia

Agricultural activities have greatly altered the global nitrogen (N) cycle and produced nitrogenous gases of environmental significance. More than half of all chemical N fertilizer produced globally is used in crop production in East, Southeast and South Asia, where rice is central to nutrition. Emissions of nitrous oxide (N₂O), nitric oxide (NO) and ammonia (NH₃) from croplands in this region were estimated by considering background emission and emissions resulting from N added to croplands, including chemical N, animal manure, biologically fixed N and N in crop residues returned to fields. Background emission fluxes of N₂O and NO from croplands were estimated to be 1.22 and 0.57 kg N ha^?1 yr^?1, respectively. Separate fertilizer‐induced emission factors were estimated for upland fields and rice fields. Total N₂O emission from croplands in the study region was estimated to be 1.19 Tg N yr^?1, with 43% contributed by background emissions. The average fertilizer‐induced N₂O emission, however, accounts for only 0.93% of the applied N, which is less than the default IPCC value of 1.25%, because of the low emission factor from paddy fields. Total NO emission was 591 Gg N yr^?1 in the study region, with 40% from background emissions. The average fertilizer‐induced NO emission factor was 0.48%. Total NH₃ emission was estimated to be 11.8 Tg N yr^?1. The use of urea and ammonium bicarbonate and the cultivation of rice led to a high average NH₃ loss rate from chemical N fertilizer in the study region. Emissions were displayed at a 0.5° × 0.5° resolution with the use of a global landuse database.     

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.     

Divergent terrestrial responses of soil N2O emissions to different levels of elevated CO2 and temperature

Understanding the responses of soil nitrous oxide (N₂O) emissions from terrestrial ecosystems to future CO₂ enrichment and warming is critical for the development of mitigation and adaptation policies. The effects of continuous increase in elevated CO₂ (EC) and elevated temperature (ET) on N₂O emissions are not fully known. We synthesized 209 measurements from 70 published studies and carried out a meta-analysis to examine individual and interactive effects of EC and ET on N₂O emissions from grasslands, croplands and forests. On average, a significant increase of 23% in N₂O emissions was observed under EC across all case studies. EC did not affect N₂O emissions from grasslands or forests, but significantly increased N₂O emissions in croplands by 38%. The extent of ET effects on N₂O emissions was nonsignificant and there was no significant difference in N₂O emission responses among these three terrestrial systems. ET only promoted N₂O emissions in forest by about 32% when ET was less than 2°C. The interactive effect of EC and ET on N₂O emissions was significantly synergistic, showing a greater increase than the sum of the effects caused by EC and ET alone. Our findings indicated that the combination of EC and ET substantially promoted soil N₂O and highlighted the urgent need to explore its mechanisms to better understand N₂O responses under future climate change.     

Spatially explicit estimates of N2O emissions from croplands suggest climate mitigation opportunities from improved fertilizer management

With increasing nitrogen (N) application to croplands required to support growing food demand, mitigating N₂O emissions from agricultural soils is a global challenge. National greenhouse gas emissions accounting typically estimates N₂O emissions at the country scale by aggregating all crops, under the assumption that N₂O emissions are linearly related to N application. However, field studies and meta‐analyses indicate a nonlinear relationship, in which N₂O emissions are relatively greater at higher N application rates. Here, we apply a super‐linear emissions response model to crop‐specific, spatially explicit synthetic N fertilizer and manure N inputs to provide subnational accounting of global N₂O emissions from croplands. We estimate 0.66 Tg of N₂O‐N direct global emissions circa 2000, with 50% of emissions concentrated in 13% of harvested area. Compared to estimates from the IPCC Tier 1 linear model, our updated N₂O emissions range from 20% to 40% lower throughout sub‐Saharan Africa and Eastern Europe, to >120% greater in some Western European countries. At low N application rates, the weak nonlinear response of N₂O emissions suggests that relatively large increases in N fertilizer application would generate relatively small increases in N₂O emissions. As aggregated fertilizer data generate underestimation bias in nonlinear models, high‐resolution N application data are critical to support accurate N₂O emissions estimates.     

Carbon balances in US croplands during the last two decades of the twentieth century

Carbon (C) added to soil as organic matter in crop residues and carbon emitted to the atmosphere as CO₂ in soil respiration are key determinants of the C balance in cropland ecosystems. We used complete and comprehensive county-level yields and area data to estimate and analyze the spatial and temporal variability of regional and national scale residue C inputs, net primary productivity (NPP), and C stocks in US croplands from 1982 to 1997. Annual residue C inputs were highest in the North Central and Central and Northern Plains regions that comprise ~70% of US cropland. Average residue C inputs ranged from 1.8 (Delta States) to 3.0 (North Central region) Mg?C?ha^?1?year^?1, and average NPP ranged from 3.1 (Delta States) to 5.4 (Far West region) Mg?C?ha^?1?year^?1. Residue C inputs tended to be inversely proportional to the mean growing season temperature. A quadratic relationship incorporating the growing season mean temperature and total precipitation closely predicted the variation in residue C inputs in the North Central region and Central and Northern Plains. We analyzed the soil C balance using the crop residue database and the Introductory Carbon Balance regional Model (ICBMr). Soil C stocks (0–20?cm) on permanent cropland ranged between 3.07 and 3.1?Pg during the study period, with an average increase of ~4?Tg?C?year^?1, during the 1990s. Interannual variability in soil C stocks ranged from 0 to 20?Tg?C (across a mean C stock of 3.08?±?0.01?Pg) during the study period; interannual variability in residue C inputs varied between 1 and 43?Tg C (across a mean input of 220?±?19?Tg). Such interannual variation has implications for national estimates of CO₂ emissions from cropland soils needed for implementation of greenhouse gas (GHG) mitigation strategies involving agriculture.     

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

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

Soil fauna diversity increases CO2 but suppresses N2O emissions from soil

Soil faunal activity can be a major control of greenhouse gas (GHG) emissions from soil. Effects of single faunal species, genera or families have been investigated, but it is unknown how soil fauna diversity may influence emissions of both carbon dioxide (CO₂, end product of decomposition of organic matter) and nitrous oxide (N₂O, an intermediate product of N transformation processes, in particular denitrification). Here, we studied how CO₂ and N₂O emissions are affected by species and species mixtures of up to eight species of detritivorous/fungivorous soil fauna from four different taxonomic groups (earthworms, potworms, mites, springtails) using a microcosm set‐up. We found that higher species richness and increased functional dissimilarity of species mixtures led to increased faunal‐induced CO₂ emission (up to 10%), but decreased N₂O emission (up to 62%). Large ecosystem engineers such as earthworms were key drivers of both CO₂ and N₂O emissions. Interestingly, increased biodiversity of other soil fauna in the presence of earthworms decreased faunal‐induced N₂O emission despite enhanced C cycling. We conclude that higher soil fauna functional diversity enhanced the intensity of belowground processes, leading to more complete litter decomposition and increased CO₂ emission, but concurrently also resulting in more complete denitrification and reduced N₂O emission. Our results suggest that increased soil fauna species diversity has the potential to mitigate emissions of N₂O from soil ecosystems. Given the loss of soil biodiversity in managed soils, our findings call for adoption of management practices that enhance soil biodiversity and stimulate a functionally diverse faunal community to reduce N₂O emissions from managed soils.     

The European carbon balance. Part 4: integration of carbon and other trace‐gas fluxes

Overviewing the European carbon (C), greenhouse gas (GHG), and non‐GHG fluxes, gross primary productivity (GPP) is about 9.3 Pg yr^?1, and fossil fuel imports are 1.6 Pg yr^?1. GPP is about 1.25% of solar radiation, containing about 360 × 10¹⁸ J energy – five times the energy content of annual fossil fuel use. Net primary production (NPP) is 50%, terrestrial net biome productivity, NBP, 3%, and the net GHG balance, NGB, 0.3% of GPP. Human harvest uses 20% of NPP or 10% of GPP, or alternatively 1‰ of solar radiation after accounting for the inherent cost of agriculture and forestry, for production of pesticides and fertilizer, the return of organic fertilizer, and for the C equivalent cost of GHG emissions. C equivalents are defined on a global warming potential with a 100‐year time horizon. The equivalent of about 2.4% of the mineral fertilizer input is emitted as N₂O. Agricultural emissions to the atmosphere are about 40% of total methane, 60% of total NO‐N, 70% of total N₂O‐N, and 95% of total NH₃‐N emissions of Europe. European soils are a net C sink (114 Tg yr^?1), but considering the emissions of GHGs, soils are a source of about 26 Tg CO₂ C‐equivalent yr^?1. Forest, grassland and sediment C sinks are offset by GHG emissions from croplands, peatlands and inland waters. Non‐GHGs (NH₃, NOx) interact significantly with the GHG and the C cycle through ammonium nitrate aerosols and dry deposition. Wet deposition of nitrogen (N) supports about 50% of forest timber growth. Land use change is regionally important. The absolute flux values total about 50 Tg C yr^?1. Nevertheless, for the European trace‐gas balance, land‐use intensity is more important than land‐use change. This study shows that emissions of GHGs and non‐GHGs significantly distort the C cycle and eliminate apparent C sinks.     

Initial nitrous oxide,carbon dioxide,and methane costs of converting conservation reserve program grassland to row crops under no‐till vs. conventional tillage

Around 4.4 million ha of land in USDA Conservation Reserve Program (CRP) contracts will expire between 2013 and 2018 and some will likely return to crop production. No‐till (NT) management offers the potential to reduce the global warming costs of CO₂, CH₄, and N₂O emissions during CRP conversion, but to date there have been no CRP conversion tillage comparisons. In 2009, we converted portions of three 9–21 ha CRP fields in Michigan to conventional tillage (CT) or NT soybean production and reserved a fourth field for reference. Both CO₂ and N₂O fluxes increased following herbicide application in all converted fields, but in the CT treatment substantial and immediate N₂O and CO₂ fluxes occurred after tillage. For the initial 201‐day conversion period, average daily N₂O fluxes (g N₂O‐N ha^?1 d^?1) were significantly different in the order: CT (47.5 ± 6.31, n = 6) ? NT (16.7 ± 2.45, n = 6) ? reference (2.51 ± 0.73, n = 4). Similarly, soil CO₂ fluxes in CT were 1.2 times those in NT and 3.1 times those in the unconverted CRP reference field. All treatments were minor sinks for CH₄ (?0.69 ± 0.42 to ?1.86 ± 0.37 g CH₄–C ha^?1 d^?1) with no significant differences among treatments. The positive global warming impact (GWI) of converted soybean fields under both CT (11.5 Mg CO₂e ha^?1) and NT (2.87 Mg CO₂e ha^?1) was in contrast to the negative GWI of the unconverted reference field (?3.5 Mg CO₂e ha^?1) with on‐going greenhouse gas (GHG) mitigation. N₂O contributed 39.3% and 55.0% of the GWI under CT and NT systems with the remainder contributed by CO₂ (60.7% and 45.0%, respectively). Including foregone mitigation, we conclude that NT management can reduce GHG costs by ~60% compared to CT during initial CRP conversion.     

A new estimation of global soil greenhouse gas fluxes using a simple data-oriented model

Soil greenhouse gas fluxes (particularly CO₂, CH₄, and N₂O) play important roles in climate change. However, despite the importance of these soil greenhouse gases, the number of reports on global soil greenhouse gas fluxes is limited. Here, new estimates are presented for global soil CO₂ emission (total soil respiration), CH₄ uptake, and N₂O emission fluxes, using a simple data-oriented model. The estimated global fluxes for CO₂ emission, CH₄ uptake, and N₂O emission were 78 Pg C yr⁻¹ (Monte Carlo 95% confidence interval, 64–95 Pg C yr⁻¹), 18 Tg C yr⁻¹ (11–23 Tg C yr⁻¹), and 4.4 Tg N yr⁻¹ (1.4–11.1 Tg N yr⁻¹), respectively. Tropical regions were the largest contributor of all of the gases, particularly the CO₂ and N₂O fluxes. The soil CO₂ and N₂O fluxes had more pronounced seasonal patterns than the soil CH₄ flux. The collected estimates, including both the previous and the present estimates, demonstrate that the means of the best estimates from each study were 79 Pg C yr⁻¹ (291 Pg CO₂ yr⁻¹; coefficient of variation, CV = 13%, N = 6) for CO₂, 21 Tg C yr⁻¹ (29 Tg CH₄ yr⁻¹; CV = 24%, N = 24) for CH₄, and 7.8 Tg N yr⁻¹ (12.2 Tg N₂O yr⁻¹; CV = 38%, N = 11) for N₂O. For N₂O, the mean of the estimates that was calculated by excluding the earliest two estimates was 6.6 Tg N yr⁻¹ (10.4 Tg N₂O yr⁻¹; CV = 22%, N = 9). The reported estimates vary and have large degrees of uncertainty but their overall magnitudes are in general agreement. To further minimize the uncertainty of soil greenhouse gas flux estimates, it is necessary to build global databases and identify key processes in describing global soil greenhouse gas fluxes.     

Effects of nitrogen deposition on the greenhouse gas fluxes from forest soils

Nitrogen (N) deposition can alter the rates of microbial N- and C- turnover, and thus can affect the fluxes of greenhouse gases (GHG, e.g., CO₂, CH₄, and N₂O) from forest soils. The effects of N deposition on the GHG fluxes from forest soils were reviewed in this paper. N deposition to forest soils have shown variable effects on the soil GHG fluxes from forest, including increases, decreases or unchanged rates depending on forest type, N status of the soil, and the rate and type of atmospheric N deposition. In forest ecosystems where biological processes are limited by N supply, N additions either stimulate soil respiration or have no significant effect, whereas in “N saturated” forest ecosystems, N additions decrease CO₂ emission, reduce CH₄ oxidation and elevate N₂O flux from the soil. The mechanisms and research methods about the effects of N deposition on GHG fluxes from forest soils were also reviewed in this paper. Finally, the present and future research needs about the effects of N deposition on the GHG fluxes from forest soils were discussed.