Soil N2O emissions with different reduced tillage methods during the establishment of Miscanthus in temperate grassland

An increase in renewable energy and the planting of perennial bioenergy crops is expected in order to meet global greenhouse gas (GHG) targets. Nitrous oxide (N₂O) is a potent greenhouse gas, and this paper addresses a knowledge gap concerning soil N₂O emissions over the possible “hot spot” of land use conversion from established pasture to the biofuel crop Miscanthus. The work aims to quantify the impacts of this land use change on N₂O fluxes using three different cultivation methods. Three replicates of four treatments were established: Miscanthus x giganteus (Mxg) planted without tillage; Mxg planted with light tillage; a novel seed‐based Miscanthus hybrid planted with light tillage under bio‐degradable mulch film; and a control of uncultivated established grass pasture with sheep grazing. Soil N₂O fluxes were recorded every 2 weeks using static chambers starting from preconversion in April 2016 and continuing until the end of October 2017. Monthly soil samples were also taken and analysed for nitrate and ammonium. There was no significant difference in N₂O emissions between the different cultivation methods. However, in comparison with the uncultivated pasture, N₂O emissions from the cultivated Miscanthus plots were 550%–819% higher in the first year (April to December 2016) and 469%–485% higher in the second year (January to October 2017). When added to an estimated carbon cost for production over a 10 year crop lifetime (including crop management, harvest, and transportation), the measured N₂O conversion cost of 4.13 Mg CO₂‐eq./ha represents a 44% increase in emission compared to the base case. This paper clearly shows the need to incorporate N₂O fluxes during Miscanthus establishment into assessments of GHG balances and life cycle analysis and provides vital knowledge needed for this process. This work therefore also helps to support policy decisions regarding the costs and benefits of land use change to Miscanthus.     

Greenhouse gas budget (CO2, CH4 and N2O) of intensively managed grassland following restoration

The first full greenhouse gas (GHG) flux budget of an intensively managed grassland in Switzerland (Chamau) is presented. The three major trace gases, carbon dioxide (CO₂), methane (CH₄), and nitrous oxide (N₂O) were measured with the eddy covariance (EC) technique. For CO₂ concentrations, an open‐path infrared gas analyzer was used, while N₂O and CH₄ concentrations were measured with a recently developed continuous‐wave quantum cascade laser absorption spectrometer (QCLAS). We investigated the magnitude of these trace gas emissions after grassland restoration, including ploughing, harrowing, sowing, and fertilization with inorganic and organic fertilizers in 2012. Large peaks of N₂O fluxes (20–50 nmol m^?2 s^?1 compared with a <5 nmol m^?2 s^?1 background) were observed during thawing of the soil after the winter period and after mineral fertilizer application followed by re‐sowing in the beginning of the summer season. Nitrous oxide (N₂O) fluxes were controlled by nitrogen input, plant productivity, soil water content and temperature. Management activities led to increased variations of N₂O fluxes up to 14 days after the management event as compared with background fluxes measured during periods without management (<5 nmol m^?2 s^?1). Fluxes of CO₂ remained small until full plant development in early summer 2012. In contrast, methane emissions showed only minor variations over time. The annual GHG flux budget was dominated by N₂O (48% contribution) and CO₂ emissions (44%). CH₄ flux contribution to the annual budget was only minor (8%). We conclude that recently developed multi‐species QCLAS in an EC system open new opportunities to determine the temporal variation of N₂O and CH₄ fluxes, which further allow to quantify annual emissions. With respect to grassland restoration, our study emphasizes the key role of N₂O and CO₂ losses after ploughing, changing a permanent grassland from a carbon sink to a significant carbon source.     

Partitioning of ecosystem respiration of CO2 released during land‐use transition from temperate agricultural grassland to Miscanthus × giganteus

Conversion of large areas of agricultural grassland is inevitable if European and UK domestic production of biomass is to play a significant role in meeting demand. Understanding the impact of these land‐use changes on soil carbon cycling and stocks depends on accurate predictions from well‐parameterized models. Key considerations are cultivation disturbance and the effect of autotrophic root input stimulation on soil carbon decomposition under novel biomass crops. This study presents partitioned parameters from the conversion of semi‐improved grassland to Miscanthus bioenergy production and compares the contribution of autotrophic and heterotrophic respiration to overall ecosystem respiration of CO₂ in the first and second years of establishment. Repeated measures of respiration from within and without root exclusion collars were used to produce time‐series model integrations separating live root inputs from decomposition of grass residues ploughed in with cultivation of the new crop. These parameters were then compared to total ecosystem respiration derived from eddy covariance sensors. Average soil surface respiration was 13.4% higher in the second growing season, increasing from 2.9 to 3.29 g CO₂‐C m^?2 day^?1. Total ecosystem respiration followed a similar trend, increasing from 4.07 to 5.4 g CO₂‐C m^?2 day^?1. Heterotrophic respiration from the root exclusion collars was 32.2% lower in the second growing season at 1.20 g CO₂‐C m^?2 day^?1 compared to the previous year at 1.77 g CO₂‐C m^?2 day^?1. Of the total respiration flux over the two‐year time period, aboveground autotrophic respiration plus litter decomposition contributed 38.46% to total ecosystem respiration while belowground autotrophic respiration and stimulation by live root inputs contributed 46.44% to soil surface respiration. This figure is notably higher than mean figures for nonforest soils derived from the literature and demonstrates the importance of crop‐specific parameterization of respiration models.     

Carbon and nitrogen dynamics in bioenergy ecosystems: 2. Potential greenhouse gas emissions and global warming intensity in the conterminous United States

This study estimated the potential emissions of greenhouse gases (GHG) from bioenergy ecosystems with a biogeochemical model AgTEM, assuming maize (Zea mays L.), switchgrass (Panicum virgatum L.), and Miscanthus (Miscanthus × giganteus) will be grown on the current maize‐producing areas in the conterminous United States. We found that the maize ecosystem acts as a mild net carbon source while cellulosic ecosystems (i.e., switchgrass and Miscanthus) act as mild sinks. Nitrogen fertilizer use is an important factor affecting biomass production and N₂O emissions, especially in the maize ecosystem. To maintain high biomass productivity, the maize ecosystem emits much more GHG, including CO₂ and N₂O, than switchgrass and Miscanthus ecosystems, when high‐rate nitrogen fertilizers are applied. For maize, the global warming potential (GWP) amounts to 1–2 Mg CO₂eq ha^?1 yr^?1, with a dominant contribution of over 90% from N₂O emissions. Cellulosic crops contribute to the GWP of less than 0.3 Mg CO₂eq ha^?1 yr^?1. Among all three bioenergy crops, Miscanthus is the most biofuel productive and the least GHG intensive at a given cropland. Regional model simulations suggested that substituting Miscanthus for maize to produce biofuel could potentially save land and reduce GHG emissions.     

Greenhouse gas budget of a poplar bioenergy plantation in Belgium: CO2 uptake outweighs CH4 and N2O emissions

Biomass from short‐rotation coppice (SRC) of woody perennials is being increasingly used as a bioenergy source to replace fossil fuels, but accurate assessments of the long‐term greenhouse gas (GHG) balance of SRC are lacking. To evaluate its mitigation potential, we monitored the GHG balance of a poplar (Populus) SRC in Flanders, Belgium, over 7 years comprising three rotations (i.e., two 2 year rotations and one 3 year rotation). In the beginning—that is, during the establishment year and during each year immediately following coppicing—the SRC plantation was a net source of GHGs. Later on—that is, during each second or third year after coppicing—the site shifted to a net sink. From the sixth year onward, there was a net cumulative GHG uptake reaching ?35.8 Mg CO₂ eq/ha during the seventh year. Over the three rotations, the total CO₂ uptake was ?51.2 Mg CO₂/ha, while the emissions of CH₄ and N₂O amounted to 8.9 and 6.5 Mg CO₂ eq/ha, respectively. As the site was non‐fertilized, non‐irrigated, and only occasionally flooded, CO₂ fluxes dominated the GHG budget. Soil disturbance after land conversion and after coppicing were the main drivers for CO₂ losses. One single N₂O pulse shortly after SRC establishment contributed significantly to the N₂O release. The results prove the potential of SRC biomass plantations to reduce GHG emissions and demonstrate that, for the poplar plantation under study, the high CO₂ uptake outweighs the emissions of non‐CO₂ greenhouse gases.     

Temporal trends in N2O flux dynamics in a Danish wetland – effects of plant‐mediated gas transport of N2O and O2 following changes in water level and soil mineral‐N availability

Temporal trends of N₂O fluxes across the soil–atmosphere interface were determined using continuous flux chamber measurements over an entire growing season of a subsurface aerating macrophyte (Phalaris arundinacea) in a nonmanaged Danish wetland. Observed N₂O fluxes were linked to changes in subsurface N₂O and O₂ concentrations, water level (WL), light intensity as well as mineral‐N availability. Weekly concentration profiles showed that seasonal variations in N₂O concentrations were directly linked to the position of the WL and O₂ availability at the capillary fringe above the WL. N₂O flux measurements showed surprisingly high temporal variability with marked changes in fluxes and shifts in flux directions from net source to net sink within hours associated with changing light conditions. Systematic diurnal shifts between net N₂O emission during day time and deposition during night time were observed when max subsurface N₂O concentrations were located below the root zone. Correlation (P < 0.001) between diurnal variations in O₂ concentrations and incoming photosynthetically active radiation highlighted the importance of plant‐driven subsoil aeration of the root zone and the associated controls on coupled nitrification/denitrification. Therefore, P. arundinacea played an important role in facilitating N₂O transport from the root zone to the atmosphere, and exclusion of the aboveground biomass in flux chamber measurements may lead to significant underestimations on net ecosystem N₂O emissions. Complex interactions between seasonal changes in O₂ and mineral‐N availability following near‐surface WL fluctuations in combination with plant‐mediated gas transport by P. arundinacea controlled the subsurface N₂O concentrations and gas transport mechanisms responsible for N₂O fluxes across the soil–atmosphere interface. Results demonstrate the necessity for addressing this high temporal variability and potential plant transport of N₂O in future studies of net N₂O exchange across the soil–atmosphere interface.     

N2O fluxes of a bio‐energy poplar plantation during a two years rotation period

Nitrous oxide emissions are of critical importance for the assumed climate neutrality of bio‐energy. In this study we report on the N₂O fluxes from a bio‐energy poplar plantation measured with eddy covariance for 2 years, after conversion of agricultural fields to few months after harvesting of the plantation. A pulse peak of N₂O was detected after the land use change and in the wake of the first heavy rainfall. The N₂O‐N emission during just a single week was 2.7 kg N₂O‐N ha^?1 which represented approximately 42% of the total N₂O‐N emitted during the 2 years of measurements. After this peak emission, N₂O fluxes were constantly rather low, not increasing after rainfall events any longer. Lowest emissions (and even N₂O sink) occurred mostly during the end of the second growing season with maximum canopy development, and water table deeper than 80 cm. Gross primary production (GPP) explained 68% of the monthly averaged variability in N₂O emission from August to December 2011. Probably N uptake by vegetation during the peak of the second growing season limited N₂O emission, which in fact increased again after the plantation was coppiced. For the majority of the measuring period, N₂O fluxes did not present a well‐defined diurnal pattern, with the exception of two periods: (1) from 19–22 August 2010 and (2) from September–November 2011. In both cases wind speed played a major role in controlling the diurnal pattern in these fluxes (explaining up to 80% of the diurnal variability in N₂O fluxes on 19–22 August 2010), whereas at the end of the second growing season (September–November 2011), GPP explained 73% of the diurnal pattern in N₂O fluxes.     

Measured and modelled effect of land‐use change from temperate grassland to Miscanthus on soil carbon stocks after 12 years

Soil organic carbon (SOC) is an important carbon pool susceptible to land‐use change (LUC). There are concerns that converting grasslands into the C₄ bioenergy crop Miscanthus (to meet demands for renewable energy) could negatively impact SOC, resulting in reductions of greenhouse gas mitigation benefits gained from using Miscanthus as a fuel. This work addresses these concerns by sampling soils (0–30 cm) from a site 12 years (T₁₂) after conversion from marginal agricultural grassland into Miscanthus x giganteus and four other novel Miscanthus hybrids. Soil samples were analysed for changes in below‐ground biomass, SOC and Miscanthus contribution to SOC (using a ¹³C natural abundance approach). Findings are compared to ECOSSE soil carbon model results (run for a LUC from grassland to Miscanthus scenario and continued grassland counterfactual), and wider implications are considered in the context of life cycle assessments based on the heating value of the dry matter (DM) feedstock. The mean T₁₂ SOC stock at the site was 8 (±1 standard error) Mg C/ha lower than baseline time zero stocks (T₀), with assessment of the five individual hybrids showing that while all had lower SOC stock than at T₀ the difference was only significant for a single hybrid. Over the longer term, new Miscanthus C₄ carbon replaces pre‐existing C₃ carbon, though not at a high enough rate to completely offset losses by the end of year 12. At the end of simulated crop lifetime (15 years), the difference in SOC stocks between the two scenarios was 4 Mg C/ha (5 g CO₂‐eq/MJ). Including modelled LUC‐induced SOC loss, along with carbon costs relating to soil nitrous oxide emissions, doubled the greenhouse gas intensity of Miscanthus to give a total global warming potential of 10 g CO₂‐eq/MJ (180 kg CO₂‐eq/Mg DM).     

Greenhouse gas emissions from the energy crop oilseed rape (Brassica napus); the role of photosynthetically active radiation in diurnal N2O flux variation

Oilseed rape (OSR, Brassica napus L.) is an important feedstock for biodiesel; hence, carbon dioxide (CO₂), methane (CH₄) and particularly fertilizer‐derived nitrous oxide (N₂O) emissions during cultivation must be quantified to assess putative greenhouse gas (GHG) savings, thus creating an urgent and increasing need for such data. Substrates of nitrification [ammonium (NH₄)] and denitrification [nitrate (NO₃)], the predominant N₂O production pathways, were supplied separately and in combination to OSR in a UK field trial aiming to: (i) produce an accurate GHG budget of fertilizer application; (ii) characterize short‐ to medium‐term variation in GHG fluxes; (iii) establish the processes driving N₂O emission. Three treatments were applied twice, 1 week apart: ammonium nitrate fertilizer (NH₄NO₃, 69 kg‐N ha^?1) mimicking the farm management, ammonium chloride (NH₄Cl, 34.4 kg‐N ha^?1) and sodium nitrate (NaNO₃, 34.6 kg‐N ha^?1). We deployed SkyLine2D for the very first time, a novel automated chamber system to measure CO_2, CH₄ and N₂O fluxes at unprecedented high temporal and spatial resolution from OSR. During 3 weeks following the fertilizer application, CH₄ fluxes were negligible, but all treatments were a net sink for CO₂ (ca. 100 g CO₂ m^?2). Cumulative N₂O emissions (ca. 120 g CO₂‐eq m^?2) from NH₄NO₃ were significantly greater (P < 0.04) than from NaNO₃ (ca. 80 g CO₂‐eq m^?2), but did not differ from NH₄Cl (ca. 100 g CO₂‐eq m^?2) and reduced the carbon sink of photosynthesis so that OSR was a net GHG source in the fertilizer treatment. Diurnal variation in N₂O emissions, peaking in the afternoon, was more strongly associated with photosynthetically active radiation (PAR) than temperature. This suggests that the supply of carbon (C) from photosynthate may have been the key driver of the observed diurnal pattern in N₂O emission and thus should be considered in future process‐based models of GHG emissions.     

Simulation of greenhouse gases following land‐use change to bioenergy crops using the ECOSSE model: a comparison between site measurements and model predictions

This article evaluates the suitability of the ECOSSE model to estimate soil greenhouse gas (GHG) fluxes from short rotation coppice willow (SRC‐Willow), short rotation forestry (SRF‐Scots Pine) and Miscanthus after land‐use change from conventional systems (grassland and arable). We simulate heterotrophic respiration (R_h), nitrous oxide (N₂O) and methane (CH₄) fluxes at four paired sites in the UK and compare them to estimates of R_h derived from the ecosystem respiration estimated from eddy covariance (EC) and R_h estimated from chamber (IRGA) measurements, as well as direct measurements of N₂O and CH₄ fluxes. Significant association between modelled and EC‐derived R_h was found under Miscanthus, with correlation coefficient (r) ranging between 0.54 and 0.70. Association between IRGA‐derived R_h and modelled outputs was statistically significant at the Aberystwyth site (r = 0.64), but not significant at the Lincolnshire site (r = 0.29). At all SRC‐Willow sites, significant association was found between modelled and measurement‐derived R_h (0.44 ≤ r ≤ 0.77); significant error was found only for the EC‐derived R_h at the Lincolnshire site. Significant association and no significant error were also found for SRF‐Scots Pine and perennial grass. For the arable fields, the modelled CO₂ correlated well just with the IRGA‐derived R_h at one site (r = 0.75). No bias in the model was found at any site, regardless of the measurement type used for the model evaluation. Across all land uses, fluxes of CH₄ and N₂O were shown to represent a small proportion of the total GHG balance; these fluxes have been modelled adequately on a monthly time‐step. This study provides confidence in using ECOSSE for predicting the impacts of future land use on GHG balance, at site level as well as at national level.     

Seasonal variation in N2O emissions from urine patches: Effects of urine concentration, soil compaction and dung

Urine patches in pastures rank among the highest sources of the greenhouse gas nitrous oxide (N₂O) from animal production systems. Previous laboratory studies indicate that N₂O emissions for urine-N in pastures may increase with a factor five or eight in combination with soil compaction and dung, respectively. These combinations of urine, compaction and dung occur regularly in pastures, especially in so-called camping areas. The aims of this study were (i) to experimentally quantify the effect of compaction and dung on emission factors of N₂O from urine patches under field conditions; (ii) to detect any seasonal changes in emission from urine patches; and (iii) to quantify possible effects of urine concentration and -volume. A series of experiments on the effects of compaction, dung, urine-N concentration and urine volume was set up at a pasture on a sandy soil (typic Endoaquoll) in Wageningen, the Netherlands. Artificial urine was applied 8 times in the period August 2000–November 2001, and N₂O emissions were monitored for a minimum of 1 month after each application. The average emission factor for urine-only treatments was 1.55%. Over the whole period, only soil compaction had a clear significant effect, raising the average N₂O emissions from urine patches from 1.30% to 2.92% of the applied N. Dung had no consistent effect; although it increased the average emissions from 1.60% to 2.82%, this was clearly significant (P< 0.01) for only one application date and marginally significant (P=0.054) for the whole experiment. Both compaction and dung increased water-filled pore space (WFPS) of the topsoil for a more prolonged time than high urine volumes. No effect of amount of urine-N or urine volume on N₂O emissions relative to added N was detected for the whole experiment. There were clear differences between application dates, with highest emissions for urine-only treatments of 4.25% in October, 2000, and lowest of –0.11% in June, 2001. Emissions peaked at 60–70% WFPS, and decreased rapidly with both higher and lower WFPS. We conclude that compaction leads to a considerable increase in the N₂O emissions under field conditions, mainly through higher WFPS. Dung addition may have the same effect, although this was not consistent throughout our experiment. Seasonal variations seemed mainly driven by differences in WFPS. Based on this study, mitigation strategies should focus on minimizing the grazing period with wet conditions leading to WFPS > 50%, avoiding camping areas in pastures, and on avoiding grazing under moist soil conditions. Greenhouse gas budgets for grazing conditions should include the effects of soil compaction and dung to represent actual emissions.     

Multivariate regulation of soil CO2 and N2O pulse emissions from agricultural soils

Climate and land‐use models project increasing occurrence of high temperature and water deficit in both agricultural production systems and terrestrial ecosystems. Episodic soil wetting and subsequent drying may increase the occurrence and magnitude of pulsed biogeochemical activity, affecting carbon (C) and nitrogen (N) cycles and influencing greenhouse gas (GHG) emissions. In this study, we provide the first data to explore the responses of carbon dioxide (CO₂) and nitrous oxide (N₂O) fluxes to (i) temperature, (ii) soil water content as percent water holding capacity (%WHC), (iii) substrate availability throughout, and (iv) multiple soil drying and rewetting (DW) events. Each of these factors and their interactions exerted effects on GHG emissions over a range of four (CO₂) and six (N₂O) orders of magnitude. Maximal CO₂ and N₂O fluxes were observed in environments combining intermediate %WHC, elevated temperature, and sufficient substrate availability. Amendments of C and N and their interactions significantly affected CO₂ and N₂O fluxes and altered their temperature sensitivities (Q₁₀) over successive DW cycles. C amendments significantly enhanced CO₂ flux, reduced N₂O flux, and decreased the Q₁₀ of both. N amendments had no effect on CO₂ flux and increased N₂O flux, while significantly depressing the Q₁₀ for CO₂, and having no effect on the Q₁₀ for N₂O. The dynamics across DW cycles could be attributed to changes in soil microbial communities as the different responses to wetting events in specific group of microorganisms, to the altered substrate availabilities, or to both. The complex interactions among parameters influencing trace gas fluxes should be incorporated into next generation earth system models to improve estimation of GHG emissions.     

A comparison of isoprene and monoterpene emission rates from the perennial bioenergy crops short‐rotation coppice willow and Miscanthus and the annual arable crops wheat and oilseed rape

Biogenic volatile organic compounds (BVOC) emissions from bioenergy crops may differ from those of conventional crops. We compared emission rates of isoprene and a number of monoterpenes from the lignocellulosic bioenergy crops short‐rotation coppice (SRC) willow and Miscanthus, with the conventional crops wheat and oilseed rape. BVOC emission rates were measured via dynamic vegetation enclosure and GC‐MS analysis approximately monthly between April 2010 and August 2012 at a location in England and from SRC willow at two locations in Scotland. The largest BVOC emission rates were measured from willow in England and varied between years. Isoprene emission rates varied between μg g^?1 h^?1. Of the monoterpenes detected from willow, α‐pinene emission rates were highest (μg g^?1 h^?1), followed by μg g^?1 h^?1 for δ‐3‐carene, μg g^?1 h^?1 for β‐pinene and μg g^?1 h^?1 for limonene. BVOC emission rates measured in Scotland were much lower. Low emission rates of isoprene and α‐pinene were measured from Miscanthus in 2010 (μg g^?1 h^?1 and μg g^?1 h^?1, respectively) but were not detected in subsequent years. Emission rates from wheat of isoprene were negligible but relatively high for monoterpenes (μg g^?1 h^?1 and μg g^?1 h^?1 for α‐pinene and limonene, respectively). No significant emission rates of BVOCs were measured from oilseed rape. The measured emission rates followed a clear seasonal trend. Crude extrapolations based solely on data gathered here indicate that isoprene emissions from willow could correspond to 0.004–0.03% (UK) and 0.76–5.5% (Europe) of current global isoprene if 50% of all land potentially available for bioenergy crops is planted with willow.     

Influence of spatially dependent,modeled soil carbon emission factors on life‐cycle greenhouse gas emissions of corn and cellulosic ethanol

Converting land to biofuel feedstock production incurs changes in soil organic carbon (SOC) that can influence biofuel life‐cycle greenhouse gas (GHG) emissions. Estimates of these land use change (LUC) and life‐cycle GHG emissions affect biofuels' attractiveness and eligibility under a number of renewable fuel policies in the USA and abroad. Modeling was used to refine the spatial resolution and depth extent of domestic estimates of SOC change for land (cropland, cropland pasture, grassland, and forest) conversion scenarios to biofuel crops (corn, corn stover, switchgrass, Miscanthus, poplar, and willow) at the county level in the USA. Results show that in most regions, conversions from cropland and cropland pasture to biofuel crops led to neutral or small levels of SOC sequestration, while conversion of grassland and forest generally caused net SOC loss. SOC change results were incorporated into the Greenhouse Gases, Regulated Emissions, and Energy use in Transportation (GREET) model to assess their influence on life‐cycle GHG emissions of corn and cellulosic ethanol. Total LUC GHG emissions (g CO₂eq MJ^?1) were 2.1–9.3 for corn‐, ?0.7 for corn stover‐, ?3.4 to 12.9 for switchgrass‐, and ?20.1 to ?6.2 for Miscanthus ethanol; these varied with SOC modeling assumptions applied. Extending the soil depth from 30 to 100 cm affected spatially explicit SOC change and overall LUC GHG emissions; however, the influence on LUC GHG emission estimates was less significant in corn and corn stover than cellulosic feedstocks. Total life‐cycle GHG emissions (g CO₂eq MJ^?1, 100 cm) were estimated to be 59–66 for corn ethanol, 14 for stover ethanol, 18–26 for switchgrass ethanol, and ?7 to ?0.6 for Miscanthus ethanol. The LUC GHG emissions associated with poplar‐ and willow‐derived ethanol may be higher than that for switchgrass ethanol due to lower biomass yield.     

Assessing the performance of the photo‐acoustic infrared gas monitor for measuring CO2, N2O,and CH4 fluxes in two major cereal rotations

Rapid, precise, and globally comparable methods for monitoring greenhouse gas (GHG) fluxes are required for accurate GHG inventories from different cropping systems and management practices. Manual gas sampling followed by gas chromatography (GC) is widely used for measuring GHG fluxes in agricultural fields, but is laborious and time‐consuming. The photo‐acoustic infrared gas monitoring system (PAS) with on‐line gas sampling is an attractive option, although it has not been evaluated for measuring GHG fluxes in cereals in general and rice in particular. We compared N₂O, CO_2, and CH₄ fluxes measured by GC and PAS from agricultural fields under the rice–wheat and maize–wheat systems during the wheat (winter), and maize/rice (monsoon) seasons in Haryana, India. All the PAS readings were corrected for baseline drifts over time and PAS‐CH₄ (PCH₄) readings in flooded rice were corrected for water vapor interferences. The PCH₄ readings in ambient air increased by 2.3 ppm for every 1000 mg cm^?3 increase in water vapor. The daily CO₂, N₂O, and CH₄ fluxes measured by GC and PAS from the same chamber were not different in 93–98% of all the measurements made but the PAS exhibited greater precision for estimates of CO₂ and N₂O fluxes in wheat and maize, and lower precision for CH₄ flux in rice, than GC. The seasonal GC‐ and PAS‐N₂O (PN₂O) fluxes in wheat and maize were not different but the PAS‐CO₂ (PCO₂) flux in wheat was 14–39% higher than that of GC. In flooded rice, the seasonal PCH₄ and PN₂O fluxes across N levels were higher than those of GC‐CH₄ and GC‐N₂O fluxes by about 2‐ and 4fold, respectively. The PAS (i) proved to be a suitable alternative to GC for N₂O and CO₂ flux measurements in wheat, and (ii) showed potential for obtaining accurate measurements of CH₄ fluxes in flooded rice after making correction for changes in humidity.     

Agricultural peatland restoration: effects of land‐use change on greenhouse gas (CO2 and CH4) fluxes in the Sacramento‐San Joaquin Delta

Agricultural drainage of organic soils has resulted in vast soil subsidence and contributed to increased atmospheric carbon dioxide (CO₂) concentrations. The Sacramento‐San Joaquin Delta in California was drained over a century ago for agriculture and human settlement and has since experienced subsidence rates that are among the highest in the world. It is recognized that drained agriculture in the Delta is unsustainable in the long‐term, and to help reverse subsidence and capture carbon (C) there is an interest in restoring drained agricultural land‐use types to flooded conditions. However, flooding may increase methane (CH₄) emissions. We conducted a full year of simultaneous eddy covariance measurements at two conventional drained agricultural peatlands (a pasture and a corn field) and three flooded land‐use types (a rice paddy and two restored wetlands) to assess the impact of drained to flooded land‐use change on CO₂ and CH₄ fluxes in the Delta. We found that the drained sites were net C and greenhouse gas (GHG) sources, releasing up to 341 g C m^?2 yr^?1 as CO₂ and 11.4 g C m^?2 yr^?1 as CH₄. Conversely, the restored wetlands were net sinks of atmospheric CO₂, sequestering up to 397 g C m^?2 yr^?1. However, they were large sources of CH₄, with emissions ranging from 39 to 53 g C m^?2 yr^?1. In terms of the full GHG budget, the restored wetlands could be either GHG sources or sinks. Although the rice paddy was a small atmospheric CO₂ sink, when considering harvest and CH₄ emissions, it acted as both a C and GHG source. Annual photosynthesis was similar between sites, but flooding at the restored sites inhibited ecosystem respiration, making them net CO₂ sinks. This study suggests that converting drained agricultural peat soils to flooded land‐use types can help reduce or reverse soil subsidence and reduce GHG emissions.     

Soil–atmosphere exchange of CH4, CO,N2O and NOx and the effects of land‐use change in the semiarid Mallee system in Southeastern Australia

The semiarid and arid zones cover a quarter of the global land area and support one‐fifth of the world's human population. A significant fraction of the global soil–atmosphere exchange for climatically active gases occurs in semiarid and arid zones yet little is known about these exchanges. A study was made of the soil–atmosphere exchange of CH₄, CO, N₂O and NO_x in the semiarid Mallee system, in north‐western Victoria, Australia, at two sites: one pristine mallee and the other cleared for approximately 65 years for farming (currently wheat). The mean (± standard error) rates of CH₄ exchange were uptakes of ?3.0 ± 0.5 ng(C) m^?2 s^?1 for the Mallee and ?6.0 ± 0.3 ng(C) m^?2 s^?1 for the Wheat. Converting mallee forest to wheat crop increases CH₄ uptake significantly. CH₄ emissions were observed in the Mallee in summer and were hypothesized to arise from termite activity. We find no evidence that in situ growing wheat plants emit CH₄, contrary to a recent report. The average CO emissions of 10.1 ± 1.8 ng(C) m^?2 s^?1 in the Mallee and 12.6 ± 2.0 ng(C) m^?2 s^?1 in the Wheat. The average N₂O emissions were 0.5 ± 0.1 ng(N) m^?2 s^?1 from the pristine Mallee and 1.4 ± 0.3 ng(N) m^?2 s^?1 from the Wheat. The experimental results show that the processes controlling these exchanges are different to those in temperate systems and are poorly understood.     

Conversion of open lands to short‐rotation woody biomass crops: site variability affects nitrogen cycling and N2O fluxes in the US Northern Lake States

Short‐rotation woody biomass crops (SRWC) have been proposed as a major feedstock source for bioenergy generation in the Northeastern US. To quantify the environmental effects and greenhouse gas (GHG) balance of crops including SRWC, investigators need spatially explicit data which encompass entire plantation cycles. A knowledge gap exists for the establishment period which makes current GHG calculations incomplete. In this study, we investigated the effects of converting pasture and hayfields to willow (Salix spp.) and hybrid‐poplar (Populus spp.) SRWC plantations on soil nitrogen (N) cycling, nitrous oxide (N₂O) emissions, and nitrate (NO₃^?) leaching at six sites of varying soil and climate conditions across northern Michigan and Wisconsin, following these plantations from pre conversion through their first 2 years. All six sites responded to establishment with increased N₂O emissions, available inorganic N, and, where it was measured, NO₃^? leaching; however, the magnitude of these impacts varied dramatically among sites. Soil NO₃^? levels varied threefold among sites, with peak extractable NO₃^? concentrations ranging from 15 to 49 g N kg^?1 soil. Leaching losses were significant and persisted through the second year, with 44–112 kg N ha^?1 leached in SRWC plots. N₂O emissions in the first growing season varied 30‐fold among sites, from 0.5 to 17.0 Mg‐CO_2eq ha^?1 (carbon dioxide equivalents). N₂O emissions over 2 years resulted in N₂O emissions due to plantation establishment that ranged from 0.60 to 22.14 Mg‐CO_2eq ha^?1 above baseline control levels across sites. The large N losses we document herein demonstrate the importance of including direct effects of land conversion in life‐cycle analysis (LCA) studies of SRWC GHG balance. Our results also demonstrate the need for better estimation of spatial variability of N cycling processes to quantify the full environmental impacts of SRWC plantations.     

Effects of elevated ozone concentration on CH4 and N2O emission from paddy soil under fully open‐air field conditions

We investigated the effects of elevated ozone concentration (E‐O₃) on CH₄ and N₂O emission from paddies with two rice cultivars: an inbred Indica cultivar Yangdao 6 (YD6) and a hybrid one II‐you 084 (IIY084), under fully open‐air field conditions in China. A mean 26.7% enhancement of ozone concentration above the ambient level (A‐O₃) significantly reduced CH₄ emission at tillering and flowering stages leading to a reduction of seasonal integral CH₄ emission by 29.6% on average across the two cultivars. The reduced CH₄ emission is associated with O₃‐induced reduction in the whole‐plant biomass (?13.2%), root biomass (?34.7%), and maximum tiller number (?10.3%), all of which curbed the carbon supply for belowground CH₄ production and its release from submerged soil to atmosphere. Although no significant difference was detected between the cultivars in the CH₄ emission response to E‐O₃, a larger decrease in CH₄ emission with IIY084 (?33.2%) than that with YD6 (?7.0%) was observed at tillering stage, which may be due to the larger reduction in tiller number in IIY084 by E‐O₃. Additionally, E‐O₃ reduced seasonal mean NO_x flux by 5.7% and 11.8% with IIY084 and YD6, respectively, but the effects were not significant statistically. We found that the relative response of CH₄ emission to E‐O₃ was not significantly different from those reported in open‐top chamber experiments. This study has thus confirmed that increasing ozone concentration would mitigate the global warming potential of CH₄ and suggested consideration of the feedback mechanism between ozone and its precursor emission into the projection of future ozone effects on terrestrial ecosystem.