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Most nitrogen (N) lost to the environment from grazed grassland is produced as a result of N excreted by livestock, released in the form of nitrous oxide (N2O) emissions, nitrate leaching and ammonia volatilisation. In addition to the N fertiliser applied, excreta deposited by grazing livestock constitute a heterogeneous excess of N, creating spatial hotspots of N losses. This study presents a yearlong N2O emissions map from a typical intensively managed temperate grassland, grazed periodically by a dairy herd. The excreta deposition mapping was undertaken using high-resolution RGB images captured with a remotely piloted aircraft system combined with N2O emissions measurements using closed statics chambers. The annual N2O emissions were estimated to be 3.36 ± 0.30 kg N2O–N ha−1 after a total N applied from fertiliser and excreta of 608 ± 40 kg N ha−1 yr−1. Emissions of N2O were 1.9, 3.6 and 4.4 times lower than that estimated using the default IPCC 2019, 2006 or country-specific emission factors, respectively. The spatial distribution and size of excreta deposits was non-uniform, and in each grazing period, an average of 15.1% of the field was covered by urine patches and 1.0% by dung deposits. Some areas of the field repeatedly received urine deposits, accounting for an estimated total of 2410 kg N ha−1. The method reported in this study can provide better estimates of how management practices can mitigate N2O emissions, to develop more efficient selective approaches to fertiliser application, targeted nitrification inhibitor application and improvements in the current N2O inventory estimation. [ABSTRACT FROM AUTHOR]

The effect of long‐term soil phosphorus (P) on in situ nitrous oxide (N2O) emissions from temperate grassland soil ecosystems is not well understood. Grasslands typically receive large nitrogen (N) inputs both from animal deposition and fertiliser application, with a large proportion of this N being lost to the environment. Understanding optimum nutrient stoichiometry by applying N fertilisers in a relative balance with P will help to reduce N losses by enabling maximum N‐uptake by plants and microbes. This study investigates the N2O response from soils of long‐term high and low P management receiving three forms of applied N at two different rates: a nitrate‐based fertiliser (KNO3) and an ammonium‐based fertiliser ([NH4]2SO4) (both at 40 Kg N ha−1), and a synthetic urine (750 Kg N ha−1). Low soil P significantly increased N2O emissions from KNO3 and (NH4)2SO4 fertilisers by over 50% and numerically increased N2O from urine by over 20%, which is suggested to be representative of the lack of significant effect of N fertilisation on N‐uptake observed in the low P soils. There was a significant positive effect of soil P on grass N‐uptake observed in the synthetic urine and KNO3 treatments, but not in the (NH4)2SO4 treatment. Low P soils had a significantly lower pH than high P soilss and responded differently to applied synthetic urine. There was also a significant effect of P level on potential nitrification which was nearly three times that of low P, but no significant difference between potential denitrification and P level. The results from this study highlight the importance of synergy between relative nutrient applications as a deficiency of one nutrient, such as P in this case, could be detrimental to the system as a whole. Optimising soil P can result in greater N uptake (over 12, 23 and 66% in (NH4)2SO4, KNO3 and synthetic urine treatments, respectively) and in reduced emissions by up to 50% representing a win‐win scenario for farmers. Highlights: P deficiency in grassland soils causes greater N2O emissions.Insufficent soil P inhibits N‐uptake, regardless of rate or form of N.Optimising soil P levels can reduce N2O emissions and improve overall NUE. [ABSTRACT FROM AUTHOR]

Rationale: N2O isotopomers are a useful tool to study soil N cycling processes. The reliability of such measurements requires a consistent set of international N2O isotope reference materials to improve inter-laboratory and inter-instrument comparability and avoid reporting inaccurate results. All these are the more important given the role of N2O in anthropogenic climate change and the pressing need to develop our understanding of soil N cycling and N2O emission to mitigate such emissions. Cavity ring-down spectroscopy (CRDS) could potentially overcome resource requirements and technical challenges, making N2O isotopomer measurements more feasible and less expensive than previous approaches (e.g., gas chromatography [GC] and isotope ratio mass spectrometry [IRMS]). Methods: A combined laser spectrometer and small sample isotope module (CRDS & SSIM) method enabled N2O concentration, δ15Nbulk, δ15Nα, δ15Nβ and site preference (SP) measurements of sample volumes <20 mL, such as static chamber samples. Sample dilution and isotopic mixing as well as N2O concentration dependence were corrected numerically. A two-point calibration procedure normalised d values to the international isotope-ratio scales. The CRDS & SSIM repeatability was determined using a reference gas (Ref Gas). CRDS & SSIM concentration measurements were compared with those obtained by GC, and the isotope ratio measurements from two different mass spectrometers were compared. Results: The repeatability (mean ± 1s; n = 10) of the CRDS & SSIM measurements of the Ref Gas was 710.64 ppb (± 8.64), 2.82? (± 0.91), 5.41? (± 2.00), 0.23? (± 0.22) and 5.18? (± 2.18) for N2O concentration, δ15Nbulk, δ15Nα, δ15Nβ and SP, respectively. The CRDS & SSIM concentration measurements were strongly correlated with GC (r = 0.99), and they were more precise than those obtained using GC except when the N2O concentrations exceeded the specified operating range. Normalising CRDS & SSIM d values to the international isotope-ratio scales using isotopic N2O standards (AK1 and Mix1) produced accurate results when the samples were bracketed within the range of the d values of the standards. The CRDS & SSIM δ15Nbulk and SP precision was approximately one order of magnitude less than the typical IRMS precision. Conclusions: CRDS & SSIM is a promising approach that enables N2O concentrations and isotope ratios to be measured by CRDS for samples <20 mL. The CRDS & SSIM repeatability makes this approach suitable for N2O "isotopomer mapping" to distinguish dominant source pathways, such as nitrification and denitrification, and requires less extensive lab resources than the traditionally used GC/IRMS. Current study limitations highlighted potential improvements for future users of this approach to consider, such as automation and physical removal of interfering trace gases before sample analysis. [ABSTRACT FROM AUTHOR]

The nitrogen (N) cycle represents one of the most well-studied systems, yet the taxonomic diversity of the organisms that contribute to it is mostly unknown, or linked to poorly characterized microbial groups. While new information has allowed functional groups to be refined, they still rely on a priori knowledge of enzymes involved and the assumption of functional conservation, with little connection to the role the transformations, plays for specific organisms. Here, we use soil microcosms to test the impact of N deposition on prokaryotic communities. By combining chemical, genomic and transcriptomic analysis, we are able to identify and link changes in community structure to specific organisms catalysing given chemical reactions. Urea deposition led to a decrease in prokaryotic richness, and a shift in community composition. This was driven by replacement of stable native populations, which utilize energy from N-linked redox reactions for physiological maintenance, with fast responding populations that use this energy for growth. This model can be used to predict response to N disturbances and allows us to identify putative life strategies of different functional and taxonomic groups, thus providing insights into how they persist in ecosystems by niche differentiation. [ABSTRACT FROM AUTHOR]

In temperate grasslands, N source influences greenhouse gas emissions. Nitrification and urea hydrolysis inhibitors can reduce these losses. The objective of this study was to evaluate the impact of N source, urease inhibitors, and nitrification inhibitors on temperate grassland yields and N uptake. Experiments were conducted at three locations over 2 years (6 site-years) on the island of Ireland, covering a range of soils and climatic conditions. Results showed that calcium ammonium nitrate (CAN), urea+N-(n-butyl) thiophosphoric triamide (NBPT), urea+NBPT+dicyandiamide (DCD), and urea had equal annual dry matter yield. Urea+DCD had lower dry matter yield than CAN for 3 site-years. Calcium ammonium nitrate and urea+NBPT consistently had the same N uptake, urea+DCD had lower N uptake than CAN in 4 of 6 site-years, urea had lower N uptake than CAN in 2 site-years, and urea+NBPT+DCD had lower N uptake than CAN in 1 site-year. Urea+NBPT is a cost-effective alternative to CAN, which is consistently equal in terms of yield and N uptake in temperate grassland. [ABSTRACT FROM AUTHOR]

An increase in mean soil surface temperature has been observed over the last century, and it is predicted to further increase in the future. The effect of increased temperature on ecosystem carbon fluxes in a permanent temperate grassland was studied in a long-term (6 years) field experiment, using multiple temperature increments induced by IR lamps. Ecosystem respiration (R-eco) and net ecosystem exchange ( NEE) were measured and modeled by a modified Lloyd and Taylor model including a soil moisture component for R-eco (average R2 of 0.78) and inclusion of a photosynthetic component based on temperature and radiation for NEE ( R2 = 0.65). Modeled NEE values ranged between 2.3 and 5.3 kg CO2 m−2 year−1, depending on treatment. An increase of 2 or 3°C led to increased carbon losses, lowering the carbon storage potential by around 4 tonnes of C ha−1 year−1. The majority of significant NEE differences were found during night-time compared to daytime. This suggests that during daytime the increased respiration could be offset by an increase in photosynthetic uptake. This was also supported by differences in δ13C and δ18O, indicating prolonged increased photosynthetic activity associated with the higher temperature treatments. However, this increase in photosynthesis was insufficient to counteract the 24 h increase in respiration, explaining the higher CO2 emissions due to elevated temperature. [ABSTRACT FROM AUTHOR]

Denitrification in pasture soils is mediated by microbial and physicochemical processes leading to nitrogen loss through the emission of N2O and N2. It is known that N2O reduction to N2 is impaired by low soil pH yet controversy remains as inconsistent use of soil pH measurement methods by researchers, and differences in analytical methods between studies, undermine direct comparison of results. In addition, the link between denitrification and N2O emissions in response to carbon (C) mineralization and pH in different pasture soils is still not well described. We hypothesized that potential denitrification rate and aerobic respiration rate would be positively associated with soils. This relationship was predicted to be more robust when a high resolution analysis is performed as opposed to a single time point comparison. We tested this by characterizing 13 different temperate pasture soils from northern and southern hemispheres sites (Ireland and New Zealand) using a fully automated-high-resolution GC detection system that allowed us to detect a wide range of gas emissions simultaneously. We also compared the impact of using different extractants for determining pH on our conclusions. In all pH measurements, soil pH was strongly and negatively associated with both N2O production index (IN2O) and N2O/(N2O+N2) product ratio. Furthermore, emission kinetics across all soils revealed that the denitrification rates under anoxic conditions (NO+N2O+N2 μmol N/h/vial) were significantly associated with C mineralization (CO2 μmol/h/vial) measured both under oxic (r2 = 0.62, p = 0.0015) and anoxic (r2 = 0.89, p<0.0001) conditions. [ABSTRACT FROM AUTHOR]

Land application of cattle slurry can result in incidental and chronic phosphorus (P) loss to waterbodies, leading to eutrophication. Chemical amendment of slurry has been proposed as a management practice, allowing slurry nutrients to remain available to plants whilst mitigating P losses in runoff. The effectiveness of amendments is well understood but their impacts on other loss pathways (so-called ‘pollution swapping’ potential) and therefore the feasibility of using such amendments has not been examined to date. The aim of this laboratory scale study was to determine how the chemical amendment of slurry affects losses of NH3, CH4, N2O, and CO2. Alum, FeCl2, Polyaluminium chloride (PAC)- and biochar reduced NH3 emissions by 92, 54, 65 and 77% compared to the slurry control, while lime increased emissions by 114%. Cumulative N2O emissions of cattle slurry increased when amended with alum and FeCl2 by 202% and 154% compared to the slurry only treatment. Lime, PAC and biochar resulted in a reduction of 44, 29 and 63% in cumulative N2O loss compared to the slurry only treatment. Addition of amendments to slurry did not significantly affect soil CO2 release during the study while CH4 emissions followed a similar trend for all of the amended slurries applied, with an initial increase in losses followed by a rapid decrease for the duration of the study. All of the amendments examined reduced the initial peak in CH4 emissions compared to the slurry only treatment. There was no significant effect of slurry amendments on global warming potential (GWP) caused by slurry land application, with the exception of biochar. After considering pollution swapping in conjunction with amendment effectiveness, the amendments recommended for further field study are PAC, alum and lime. This study has also shown that biochar has potential to reduce GHG losses arising from slurry application. [ABSTRACT FROM AUTHOR]

Nitrous oxide (N2O) emissions are subject to intra- and interannual variation due to changes in weather and management. This creates significant uncertainties when quantifying estimates of annual N2O emissions from grazed grasslands. Despite these uncertainties, the majority of studies are short-term in nature (<1 year) and as a consequence, there is a lack of data on interannual variation in N2O emissions. The objectives of this study were to (i) quantify annual N2O emissions and (ii) assess the causes of interannual variation in emissions from grazed perennial ryegrass/white clover grassland. Nitrous oxide emissions were measured from fertilized and grazed perennial ryegrass/white clover grassland (WC) and from perennial ryegrass plots that were not grazed and did not receive N input (GB), over 4 years from 2008 to 2012 in Ireland (52°51'N, 08°21'W). The annual N2O-N emissions (kg ha-1; mean ± SE) ranged from 4.4 ± 0.2 to 34.4 ± 5.5 from WC and from 1.7 ± 0.8 to 6.3 ± 1.2 from GB. Interannual variation in N2O emissions was attributed to differences in annual rainfall, monthly (December) soil temperatures and variation in N input. Such substantial interannual variation in N2O emissions highlights the need for long-term studies of emissions from managed pastoral systems. [ABSTRACT FROM AUTHOR]

Bioenergy from crops is expected to make a considerable contribution to climate change mitigation. However, bioenergy is not necessarily carbon neutral because emissions of CO2, N2O and CH4 during crop production may reduce or completely counterbalance CO2 savings of the substituted fossil fuels. These greenhouse gases ( GHGs) need to be included into the carbon footprint calculation of different bioenergy crops under a range of soil conditions and management practices. This review compiles existing knowledge on agronomic and environmental constraints and GHG balances of the major European bioenergy crops, although it focuses on dedicated perennial crops such as M iscanthus and short rotation coppice species. Such second-generation crops account for only 3% of the current European bioenergy production, but field data suggest they emit 40% to >99% less N2O than conventional annual crops. This is a result of lower fertilizer requirements as well as a higher N-use efficiency, due to effective N-recycling. Perennial energy crops have the potential to sequester additional carbon in soil biomass if established on former cropland (0.44 Mg soil C ha−1 yr−1 for poplar and willow and 0.66 Mg soil C ha−1 yr−1 for M iscanthus). However, there was no positive or even negative effects on the C balance if energy crops are established on former grassland. Increased bioenergy production may also result in direct and indirect land-use changes with potential high C losses when native vegetation is converted to annual crops. Although dedicated perennial energy crops have a high potential to improve the GHG balance of bioenergy production, several agronomic and economic constraints still have to be overcome. [ABSTRACT FROM AUTHOR]

The effects of slurry application method and weather conditions after application on ammonia volatilisation are well documented, however, the effect on slurry N recovery in herbage is less evident due to large variability of results. The objective of this field experiment was to determine the recovery of cattle slurry NH4-N in herbage and soil in the year of application as affected by application method (trailing shoe versus broadcast) and season of application (spring versus summer), using 15N as a tracer. In 2007 and 2008, 15N enriched slurry was applied on grassland plots. N recovery in herbage and soil during the year of application was determined. Both spring and trailing shoe application resulted in significantly higher herbage DM yields, N uptake and an increased recovery of 15NH4-N in herbage. Additionally, the recovery of slurry 15NH4-N in the soil at the end of the growing season was increased. Spring and trailing shoe application reduced the losses of slurry 15NH4-N by on average 14 and 18 percentage points, respectively, which corresponded closely to ammonia volatilisation as predicted by the ALFAM model. It was concluded that slurry N recovery in temperate pasture systems can be increased by adjusting the slurry application method or timing. [ABSTRACT FROM AUTHOR]

Perennial species with the C4 pathway hold promise for biomass-based energy sources. We have explored the extent that CO2 uptake of such species may be limited by light in a temperate climate. One energetic cost of the C4 pathway is the leakiness (Φ) of bundle sheath tissues, whereby a variable proportion of the CO2. concentrated in bundle sheath cells, retrodiffuses back to the mesophyll. In this study, we scale Φ from leaf to canopy level of a Miscanthus crop (Miscanthus X giganteus hybrid) under field conditions and model the likely limitations to CO2 fixation. At the leaf level, measurements of photosynthesis coupled to online carbon isotope discrimination showed that leaves within a 3.3-m canopy (leaf area index = 8.3) show a progressive increase in both carbon isotope discrimination and Φ as light decreases. A similar increase was observed at the ecosystem scale when we used eddy covariance net ecosystem CO2 fluxes, together with isotopic profiles, to partition photosynthetic and respiratory isotopic flux densities (isofluxes) and derive canopy carbon isotope discrimination as an integrated proxy for Φ at the canopy level. Modeled values of canopy CO2 fixation using leaf-level measurements of Φ suggest that around 32% of potential photosynthetic carbon gain is lost due to light limitation, whereas using 4 determined independently from isofluxes at the canopy level the reduction in canopy CO2 uptake is estimated at 14%. Based on these results, we identify 4' as an important limitation to CO2 uptake of crops with the C4 pathway. [ABSTRACT FROM AUTHOR]

The magnitude of fractionation during photorespiration and the effect on net photosynthetic 13C discrimination (Δ) were investigated for three Senecio species, S. squalidus, S. cineraria, and S. greyii. We determined the contributions of different processes during photosynthesis to Δ by comparing observations (Δobs) with discrimination predicted from gas-exchange measurements (Δpred). Photorespiration rates were manipulated by altering the O2 partial pressure (pO2) in the air surrounding the leaves. Contributions from 13C-depleted photorespiratory CO2 were largest at high pO2. The parameters for photorespiratory fractionation (f), net fractionation during carboxylation by Rubisco and phosphoenolpyruvate carboxylase (b), and mesophyll conductance (gi) were determined simultaneously for all measurements. Instead of using Δobs data to obtain gi and f successively, which requires that b is known, we treated b,f, and gi as unknowns. We propose this as an alternative approach to analyze measurements under field conditions when b and gi are not known or cannot be determined in separate experiments. Good agreement between modeled and observed Δ was achieved with f = 11.6‰ ± 1.5‰, b = 26.0‰ ± 0.3‰, and gi of 0.27 ± 0.01,0.25 ± 0.01, and 0.22 ± 0.01 mol m-1 s-1 for S. squalidus, S. cineraria, and S. greyii, respectively. We estimate that photorespiratory fractionation decreases Δ by about 1.2‰ on average under field conditions. In addition, diurnal changes in Δ are likely to reflect variations in photorespiration even at the canopy level. Our results emphasize that the effects of photorespiration must be taken into account when partitioning net CO2 exchange of ecosystems into gross fluxes of photosynthesis and respiration. [ABSTRACT FROM AUTHOR]

Nitrogen fertiliser application represents the largest anthropogenic source of nitrous oxide (N2O) emissions, and the magnitude of these emissions is dependent on the type of fertilisers applied in the agroecosystems. Despite N-P-K compound fertilisers being commonly used in agricultural soils, a lack of information exists regarding their effects on N2O emissions. This study aims at examining the effects of different commonly used N-P-K compound fertiliser formulations with contrasting nitrate to ammonium ratios (0.05 to 0.88) on N2O emissions, yield, and nitrogen use efficiency (NUE) in temperate grassland and to compare these variables with common straight N fertilisers. Compound fertilisers with varying NPK inclusion rates (18-6-12, 10-10-20, 24-2.2-4.5, and 27-2.5-5), and calcium ammonium nitrate (CAN) and urea + N-(n-butyl) thiophosphoric triamide (NBPT) were applied at 80 kg N ha−1 to experimental plots in managed grassland on two occasions in a growing season. Fluxes of N2O during the experiment period, yield and NUE following two harvests were measured. The cumulative N2O emission from urea + NBPT, 18-6-12, 10-10-20, and 24-2.2-4.5 treatments were significantly reduced by 44%, 43%, 37%, and 31% compared with CAN treatment under conducive soil moisture condition. Under the same soil condition, 18-6-12 and 10-10-20 treatments showed higher yield, N uptake, and NUE although did not significantly differ from the other fertiliser treatments. Our results suggest that ammonium-based compound fertilisers have a potential to reduce N2O emissions while maintaining yields. Further long-term study is needed to capture the full magnitude of variations in N2O emissions, including ammonia (NH3) volatilization from nitrate and ammonium-based compound fertiliser applications from multiple soil types and under different climatic conditions. [ABSTRACT FROM AUTHOR]

Ruminant urine patches on grazed grassland are a significant source of agricultural nitrous oxide (N2O) emissions. Of the many biotic and abiotic N2O production mechanisms initiated following urine-urea deposition, codenitrification resulting in the formation of hybrid N2O, is one of the least understood. Codenitrification forms hybrid N2O via biotic N-nitrosation, co-metabolising organic and inorganic N compounds (N substrates) to produce N2O. The objective of this study was to assess the relative significance of different N substrates on codenitrification and to determine the contributions of fungi and bacteria to codenitrification. 15N-labelled ammonium, hydroxylamine (NH2OH) and two amino acids (phenylalanine or glycine) were applied, separately, to sieved soil mesocosms eight days after a simulated urine event, in the absence or presence of bacterial and fungal inhibitors. Soil chemical variables and N2O fluxes were monitored and the codenitrified N2O fluxes determined. Fungal inhibition decreased N2O fluxes by ca. 40% for both amino acid treatments, while bacterial inhibition only decreased the N2O flux of the glycine treatment, by 14%. Hydroxylamine (NH2OH) generated the highest N2O fluxes which declined with either fungal or bacterial inhibition alone, while combined inhibition resulted in a 60% decrease in the N2O flux. All the N substrates examined participated to some extent in codenitrification. Trends for codenitrification under the NH2OH substrate treatment followed those of total N2O fluxes (85.7% of total N2O flux). Codenitrification fluxes under non-NH2OH substrate treatments (0.7–1.2% of total N2O flux) were two orders of magnitude lower, and significant decreases in these treatments only occurred with fungal inhibition in the amino acid substrate treatments. These results demonstrate that in situ studies are required to better understand the dynamics of codenitrification substrates in grazed pasture soils and the associated role that fungi have with respect to codenitrification. [ABSTRACT FROM AUTHOR]

Soil plays a key role in the global carbon (C) cycle. Most current assessments of SOC stocks and the guidelines given by Intergovernmental Panel on Climate Change (IPCC) focus on the top 30 cm of soil. Our research shows that, when considering only total quantities, most of the SOC stocks are found in this top layer. However, not all forms of SOC are equally valuable as long-term stable stores of carbon: the majority of SOC is available for mineralisation and can potentially be re-emitted to the atmosphere. SOC associated with micro-aggregates and silt plus clay fractions is more stable and therefore represents a long-term carbon store. Our research shows that most of this stable carbon is located at depths below 30 cm (42% of subsoil SOC is located in microaggregates and silt and clay, compared to 16% in the topsoil), specifically in soils that are subject to clay illuviation. This has implications for land management decisions in temperate grassland regions, defining the trade-offs between primary productivity and C emissions in clay-illuviated soils, as a result of drainage. Therefore, climate smart land management should consider the balance between SOC stabilisation in topsoils for productivity versus sequestration in subsoils for climate mitigation. [ABSTRACT FROM AUTHOR]