Effect of soil aggregate size and dicyandiamide on N2O emissions and ammonia oxidizer abundance in a grazed pasture soil

Nitrous oxide (N₂O) is a potent greenhouse gas, which is mainly produced from agricultural soils. Ammonia oxidation is the rate‐determining step in N₂O production, and the process is carried out by ammonia oxidizers, bacteria and archaea. Soil aggregate size has been shown to alter soil properties, which affect N₂O emissions and bacterial communities. However, the effect of aggregate size on temporal and total N₂O emissions and ammonia‐oxidizing bacteria (AOB) and archaea (AOA) is not fully understood. This incubation study investigated the effect of three different soil aggregate sizes on N₂O emissions and ammonia oxidizer abundance under high urine‐N concentrations and the effectiveness of a nitrification inhibitor, dicyandiamide (DCD), at reducing N₂O emissions in different aggregate soils. It was found that temporal patterns of N₂O emissions were affected by aggregate size with higher peak emissions in the large and medium aggregates. However, the total emissions were the same due to a ‘switch’ in emissions at day 66, after which smaller aggregates produced higher N₂O emissions. It is suggested that the switch was caused by an increase in aggregate disruption in the small aggregates, following the urine application, due to their higher surface area to volume ratio. AOB and AOA abundances were not significantly affected by aggregate size. DCD was effective in reducing N₂O emissions in all aggregate sizes by an average of 79%. These results suggest that similar ammonia oxidizer abundance is found in soils of different aggregate sizes, and the efficacy of DCD in reducing N₂O emissions was not affected by aggregate size of the soil.     

Effects of aggregate size,soil compaction,and bovine urine on N2O emissions from a pasture soil

The dominant N₂O emission source in New Zealand, calculated using the Intergovernmental Panel on Climate Change methodology, is agricultural soils. The largest source of N₂O emissions in New Zealand occurs as a result of excreta deposition onto pasture during grazing. There is a dearth of studies examining the effect of soil compaction and soil aggregate size on N₂O emissions from urine patches in grazed pastures. In this study, we repacked soil cores with four different soil aggregate sizes (<1.0–5.6 mm diameter), applied bovine urine, and then subjected the soil cores to four levels of soil compaction. Fluxes of N₂O were monitored for 37 days after which soil cores were allowed to dry out prior to a rewetting event. There was an interaction between aggregate size and soil compaction with the cumulative loss of N₂O over the first 37 days ranging from 0.3% to 9.6% of the urine-N applied. The highest N₂O emissions occurred from the smallest and most compacted aggregates. Even under the highest levels of compaction the N₂O loss from the large aggregates (4.0–5.6 mm diameter) was <1% of the urine-N applied. Reasons for the observed differences in the N₂O flux from the different-sized aggregates included varying gas diffusivities and higher rates of denitrification in the smallest aggregates, as evidenced by the disappearance of nitrate.     

Combined effects of nitrogen deposition and biochar application on emissions of N2O,CO2 and NH3 from agricultural and forest soils

Abstract

Both nitrogen (N) deposition and biochar can affect the emissions of nitrous oxide (N₂O), carbon dioxide (CO₂) and ammonia (NH₃) from different soils. Here, we have established a simulated wet N deposition experiment to investigate the effects of N deposition and biochar addition on N₂O and CO₂ emissions and NH₃ volatilization from agricultural and forest soils. Repacked soil columns were subjected to six N deposition events over a 1-year period. N was applied at rates of 0 (N0), 60 (N60), and 120 (N120) kg Nh a^?1 yr^?1 without or with biochar (0 and 30 t ha^?1 yr^?1). For agricultural soil, adding N increased cumulative N₂O emissions by 29.8% and 99.1% (p < 0.05) from the N60 and N120 treatments, respectively as compared to without N treatments, and N120 emitted 53.4% more (p < 0.05) N₂O than the N60 treatment; NH₃ volatilization increased by 33.6% and 91.9% (p < 0.05) from the N60 and N120 treatments, respectively, as compared to without N treatments, and N120 emitted 43.6% more (p < 0.05) NH₃ than N60; cumulative CO₂ emissions were not influenced by N addition. For forest soil, adding N significantly increased cumulative N₂O emissions by 141.2% (p < 0.05) and 323.0% (p < 0.05) from N60 and N120 treatments, respectively, as compared to without N treatments, and N120 emitted 75.4% more (p < 0.05) N₂O than N60; NH₃ volatilization increased by 39.0% (p < 0.05) and 56.1% (p < 0.05) from the N60 and N120 treatments, respectively, as compared to without N treatments, and there was no obvious difference between N120 and N60 treatments; cumulative CO₂ emissions were not influenced by N addition. Biochar amendment significantly (p < 0.05) decreased cumulative N₂O emissions by 20.2% and 25.5% from agricultural and forest soils, respectively, and increased CO₂ emissions slightly by 7.2% and NH₃ volatilization obviously by 21.0% in the agricultural soil, while significantly decreasing CO₂ emissions by 31.5% and NH₃ volatilization by 22.5% in the forest soil. These results suggest that N deposition would strengthen N₂O and NH₃ emissions and have no effect on CO₂ emissions in both soils, and treatments receiving the higher N rate at N120 emitted obviously more N₂O and NH₃ than the lower rate at N60. Under the simulated N deposition circumstances, biochar incorporation suppressed N₂O emissions in both soils, and produced contrasting effects on CO₂ and NH₃ emissions, being enhanced in the agricultural soil while suppressed in the forest soil.     

N2O, NH3 and NOx Emissions as a Function of Urea Granule Size and Soil Type Under Aerobic Conditions

We examined the influence of various urea granule sizes (< 2, 7.0, 9.9 and 12.7 mm) applied into a silt loam soil (experiment 1) and soil types (sandy, silt and clay loam) treated with the largest granule (experiment 2) on gaseous N loss (except N₂) at field capacity. The prilled urea (PU) was mixed into the soil whereas the urea granules were point-placed at a 5.0-cm depth. For experiment 1, N₂O emission was enhanced with increasing granule size, ranging from 0.17–0.50% of the added N during the 45-day incubation period. In the case of experiment 2, the sandy loam soil (0.59%) behaved similarly with the silt loam (0.53%) but both showed remarkably lower emissions than were found for the clay loam soil (2.61%). Both nitrification and N₂O emissions were delayed by several days with increasing granule size, and the latter was influenced by mineral N, soil water and pH. By contrast, the NH₃ volatilization decreased with increasing granule size, implying the inhibition of urease activity by urea concentration gradients. Considering both experimental results, the NH₃ loss was highest for the PU-treated (1.73%) and the larger granules regardless of soil type did not emit more than 0.27% of the added N over 22 days, possibly because the high concentrations of either mineral N or NH₄ ⁺ in the soil surface layer (0–2.5 cm) and the high H₊ buffering capacity might regulate the NH₃ emission. Similar to the pattern of NH₃ loss, NO_x emission was noticeably higher for the PU-treated soil (0.97%) than for the larger granule sizes (0.09–0.29%), which were the highest for the sandy and clay loam soils. Positional differences in the concentration of mineral N and nitrification also influenced the NO_x emission. As such, total NH₃ loss was proportional to total NO_x emission, indicating similar influence of soil and environmental conditions on both. Pooled total N₂O, NH₃ and NO_x emission data suggest that the PU-treated soil could induce greater gaseous N loss over larger urea granules, largely in the form of NH₃ and NO_x emissions, whereas a similar increase with the largest granule size was mainly due to the total N₂O flux.     

Compaction influences N2O and N2 emissions from 15N-labeled synthetic urine in wet soils during successive saturation/drainage cycles

Nitrous oxide emitted from urine patches is a key source of agricultural greenhouse gas emissions. A better understanding of the complex soil environmental and biochemical regulation of urine-N transformations in wet soils is needed to predict N₂O emissions from grazing and also to develop targeted mitigation technologies. Soil aeration, gas diffusion and drainage are key factors regulating N transformations and are affected by compaction during grazing. To understand how soil compaction from animal treading influences N transformations of urine in wet soils, we applied pressures of 0, 220 and 400 kPa to repacked soil cores, followed by ¹⁵N-labeled synthetic urine, and then subjected the cores to three successive saturation–drainage cycles on tension tables from 0 to 10 kPa.Compaction had a relatively small effect on soil bulk density (increasing from 0.81 to 0.88 Mg m⁻³), but strongly affected the pore size distribution. Compaction reduced both total soil porosity and macroporosity. It also affected the pore size distribution, principally by decreasing the proportion of 30–60 μm and 60–100 μm pores and increasing the proportion of micropores (<30 μm).Rates of urine-N transformations, emissions of N₂ and N₂O, and the N₂O to N₂ ratio were affected by the saturation/drainage cycles and degree of compaction. During the first saturation–drainage cycle, production of both N₂O and N₂ was low (<0.4 mg N m⁻² h⁻¹), probably because of anaerobic conditions inhibiting nitrification. In the second saturation/drainage cycle, the predominant product was N₂ at all compaction rates. By the third cycle, with increasing availability of mineral-N substrates, N₂O was the dominant product in the uncompacted (max = 4.70 mg N m⁻² h⁻¹) and 220 kPa compacted soils (max = 7.65 mg N m⁻² h⁻¹) with lower amounts of N₂ produced, while N₂ was produced in similar quantities to N₂O (max = 3.11 mg N m⁻² h⁻¹) in the 400 kPa compacted soil. Reduced macroporosity in the most compacted soil contributed to more sustained N₂ and N₂O production as the soils drained. In addition, compaction affected the rate of change of soil pH and DOC, both of which affected the N₂O to N₂ ratio.Denitrification during drainage and re-saturation may make a large contribution to soil N₂O emissions. Improving soil drainage and adopting grazing management practices that avoid soil compaction while increasing macroporosity will reduce total N₂O and N₂ emissions.     

Soil engineering ants increase CO2 and N2O emissions by affecting mound soil physicochemical characteristics from a marsh soil: A laboratory study

As ecosystem engineers, ants can mediate soil processes and functions by producing biogenic structures. In their mounds, ants not only directly produce CO₂ by respiration, but may also indirectly impact soil greenhouse gas emissions by affecting substrate availability and soil physicochemical characteristics. Recent studies focused on overall gas production from ant mounds. However, little is known about mound material respiration and N₂O emissions in ant mounds in wetlands. We measured CO₂ and N₂O emissions from mound soils of three different ant species (Lasius niger Linnaeus, Lasius flavus Fabricius, and Formica candida Smith) and natural marsh soils in a laboratory incubation experiment. On the whole, average soil CO₂ and N₂O emission rates from ant mounds were significantly higher than from the natural marsh soils. Over the 64 days incubation, the cumulative soil CO₂ and N₂O production from ant mounds was, respectively, 1.5–3.0 and 1.9–50.2 times higher than from the natural soils. Soil gas emissions from ant mounds were significantly influenced by the specific ant species, with soil CO₂ and N₂O emissions from L. niger mounds being higher than those from F. candida or L. flavus mound soils. Cumulative CO₂ and N₂O emissions from ant mound soils were positively correlated with soil clay, total carbon, dissolved organic carbon, total nitrogen and NH₄⁺ content. Our laboratory results indicated that mound soil is an important source of CO₂ and N₂O emission from ant mounds in marshes, making mounds potential “hot spots” for CO₂ and N₂O emissions. Ants may increase the spatial heterogeneity of soil gas emissions by changing mound soil physicochemical properties, especially carbon and nutrition content, and soil texture. Contributions from ant mound materials should be considered when describing soil C and N cycles and their driving factors in wetland ecosystems.     

N2O emissions from humid tropical agricultural soils: effects of soil moisture,texture and nitrogen availability

We studied soil moisture dynamics and nitrous oxide (N₂O) fluxes from agricultural soils in the humid tropics of Costa Rica. Using a split-plot design on two soils (clay, loam) we compared two crop types (annual, perennial) each unfertilized and fertilized. Both soils are of andic origin. Their properties include relatively low bulk density and high organic matter content, water retention capacity, and hydraulic conductivity. The top 2–3 cm of the soils consists of distinct small aggregates (dia. <0.5 cm). We measured a strong gradient of bulk density and moisture within the top 7 cm of the clay soil. Using automated sampling and analysis systems we measured N₂O emissions at 4.6 h intervals, meteorological variables, soil moisture, and temperature at 0.5 h intervals. Mean daily soil moisture content at 5 cm depth ranged from 46% water filled pore space (WFPS) on clay in April 1995 to near saturation on loam during a wet period in February 1996. On both soils the aggregated surface layer always remained unsaturated. Soils emitted N₂O throughout the year. Mean N₂O fluxes were 1.04±0.72 ng N₂O-N cm⁻² h⁻¹ (mean±standard deviation) from unfertilized loam under annual crops compared to 3.54±4.31 ng N₂O-N cm⁻² h⁻¹ from the fertilized plot (351 days measurement). Fertilization dominated the temporal variation of N₂O emissions. Generally fluxes peaked shortly after fertilization and were increased for up to 6 weeks (‘post fertilization flux’). Emissions continued at a lower rate (‘background flux’) after fertilization effects faded. Mean post-fertilization fluxes were 6.3±6.5 ng N₂O-N cm⁻² h⁻¹ while the background flux rate was 2.2±1.8 ng N₂O-N cm⁻² h⁻¹. Soil moisture dynamics affected N₂O emissions. Post fertilization fluxes were highest from wet soils; fluxes from relatively dry soils increased only after rain events. N₂O emissions were weakly affected by soil moisture during phases of low N availability. Statistical modeling confirmed N availability and soil moisture as the major controls on N₂O flux. Our data suggest that small-scale differences in soil structure and moisture content cause very different biogeochemical environments within the top 7 cm of soils, which is important for net N₂O fluxes from soils.     

Effect of different biochar and fertilizer types on N2O and NO emissions

The use of biochar as soil improver and climate change mitigation strategy has gained much attention, although at present the effects of biochar on soil properties and greenhouse gas emissions are not completely understood. The objective of our incubation study was to investigate biochar's effect on N₂O and NO emissions from an agricultural Luvisol upon fertilizer (urea, NH₄Cl or KNO₃) application. Seven biochar types were used, which were produced from four different feedstocks pyrolyzed at various temperatures. At the end of the experiment, after 14 days of incubation, soil nitrate concentrations were decreased upon biochar addition in all fertilizer treatments by 6–16%. Biochar application decreased both cumulative N₂O (52–84%) and NO (47–67%) emissions compared to a corresponding treatment without biochar after urea and nitrate fertilizer application, and only NO emissions after ammonium application. N₂O emissions were more decreased at high compared to low pyrolysis temperature.Several hypotheses for our observations exist, which were assessed against current literature and discussed thoroughly. In our study, the decreased N₂O and NO emissions are expected to be mediated by multiple interacting phenomena such as stimulated NH₃ volatilization, microbial N immobilization, non-electrostatic sorption of NH₄⁺ and NO₃⁻, and biochar pH effects.     

Biochar suppresses N2O emissions while maintaining N availability in a sandy loam soil

Nitrous oxide (N₂O) from agricultural soil is a significant source of greenhouse gas emissions. Biochar amendment can contribute to climate change mitigation by suppressing emissions of N₂O from soil, although the mechanisms underlying this effect are poorly understood. We investigated the effect of biochar on soil N₂O emissions and N cycling processes by quantifying soil N immobilisation, denitrification, nitrification and mineralisation rates using ¹⁵N pool dilution techniques and the FLUAZ numerical calculation model. We then examined whether biochar amendment affected N₂O emissions and the availability and transformations of N in soils.Our results show that biochar suppressed cumulative soil N₂O production by 91% in near-saturated, fertilised soils. Cumulative denitrification was reduced by 37%, which accounted for 85–95 % of soil N₂O emissions. We also found that physical/chemical and biological ammonium (NH₄⁺) immobilisation increased with biochar amendment but that nitrate (NO₃⁻) immobilisation decreased. We concluded that this immobilisation was insignificant compared to total soil inorganic N content. In contrast, soil N mineralisation significantly increased by 269% and nitrification by 34% in biochar-amended soil.These findings demonstrate that biochar amendment did not limit inorganic N availability to nitrifiers and denitrifiers, therefore limitations in soil NH₄⁺ and NO₃⁻ supply cannot explain the suppression of N₂O emissions. These results support the concept that biochar application to soil could significantly mitigate agricultural N₂O emissions through altering N transformations, and underpin efforts to develop climate-friendly agricultural management techniques.     

Comparison of the effectiveness of a nitrification inhibitor, dicyandiamide, in reducing nitrous oxide emissions in four different soils under different climatic and management conditions

Nitrous oxide (N₂O) is a potent greenhouse gas and, in New Zealand, about one‐third of the total greenhouse gas emissions from the agricultural sector are of N₂O, mostly derived from animal excreta in grazed pasture soils. The aim of this study was to determine the effectiveness of a nitrification inhibitor, dicyandiamide (DCD), in reducing N₂O emissions from animal urine patches in four different soils located in different regions of New Zealand with different soil, climatic and management conditions. The four soils are Templeton fine sandy loam and Lismore stony silt loam in Canterbury in the South Island, Horotiu silt loam in the Waikato region and Taupo pumice sand near Lake Taupo, both in the North Island. Results showed that the application of a fine‐particle suspension nitrification inhibitor, DCD, to grazed pasture soils was very effective in reducing N₂O emissions in all four different soils. Total N₂O emissions (over 69–137 days) from animal urine patches ranged from 1 to 20.9 kg N₂O‐N ha^?1 without DCD. These were reduced to 0.31–5.7 kg N₂O‐N ha^?1 by the use of DCD, representing 61–73% reductions (with an average of 70% reduction). The N₂O‐N emission factor from animal urine N, EF₃, was reduced from an average of 0.9 to 0.3% by the use of DCD. These results demonstrate the potential of using nitrification inhibitors to mitigate N₂O emissions in a wide range of grazed pasture soils under different climatic and management conditions.     

林分类型和氮添加对亚热带森林土壤氧化亚氮排放的影响

为揭示亚热带森林土壤N₂O排放对林分类型和氮添加的响应特征,选取位于福建省三明市的中亚热带米槠次生林、杉木人工林和马尾松人工林土壤为研究对象,分别设置无氮添加(N0 mg/kg)、低氮添加(N10 mg/kg)、中氮添加(N25 mg/kg)和高氮添加(N50 mg/kg)4个氮添加水平,进行微宇宙培养试验,测定土壤N₂O排放。结果表明：与无氮添加处理相比,氮添加整体上降低3种林分土壤pH,增加土壤NH₄⁺-N和NO₃^--N含量。无氮添加处理中杉木人工林和马尾松人工林土壤N₂O累积排放量分别为9.67和9.62 mg/kg,显著高于米槠次生林土壤N₂O累积排放量6.81 mg/kg。低氮添加处理中杉木人工林和马尾松人工林土壤N₂O累积排放量显著高于米槠次生林。但在中氮和高氮添加处理中,3种林分土壤N₂O累积排放量均无显著性差异。不同氮添加处理均促进3种林分土壤N     

Effects of soil moisture on gross N transformations and N2O emission in acid subtropical forest soils

Soil moisture changes, arising from seasonal variation or from global climate changes, could influence soil nitrogen (N) transformation rates and N availability in unfertilized subtropical forests. A ¹⁵?N dilution study was carried out to investigate the effects of soil moisture change (30–90 % water-holding capacity (WHC)) on potential gross N transformation rates and N₂O and NO emissions in two contrasting (broad-leaved vs. coniferous) subtropical forest soils. Gross N mineralization rates were more sensitive to soil moisture change than gross NH₄ ⁺ immobilization rates for both forest soils. Gross nitrification rates gradually increased with increasing soil moisture in both forest soils. Thus, enhanced N availability at higher soil moisture values was attributed to increasing gross N mineralization and nitrification rates over the immobilization rate. The natural N enrichment in humid subtropical forest soils may partially be due to fast N mineralization and nitrification under relatively higher soil moisture. In broad-leaved forest soil, the high N₂O and NO emissions occurred at 30 % WHC, while the reverse was true in coniferous forest soil. Therefore, we propose that there are different mechanisms regulating N₂O and NO emissions between broad-leaved and coniferous forest soils. In coniferous forest soil, nitrification may be the primary process responsible for N₂O and NO emissions, while in broad-leaved forest soil, N₂O and NO emissions may originate from the denitrification process.     

Abiotic nitrous oxide production from hydroxylamine in soils and their dependence on soil properties

Despite the fact that microbial nitrification and denitrification are considered the major soil N₂O emission sources, especially from agricultural soils, several abiotic reactions involving the nitrification intermediate hydroxylamine (NH₂OH) have been identified leading to N₂O emissions, but are being neglected in most current studies. Here, we studied N₂O formation from NH₂OH in cropland, grassland, and forest soils in laboratory incubation experiments. Incubations were conducted with and without the addition of NH₂OH to non-sterile and sterile soil samples. N₂O evolution was quantified with gas chromatography and further analyzed with online laser absorption spectroscopy. Additionally, the isotopic signature of the produced N₂O (δ¹⁵N, δ¹⁸O, and ¹⁵N site preference) was analyzed with isotope ratio mass spectrometry. While the forest soil samples showed hardly any N₂O evolution upon the addition of NH₂OH, immediate and very large formation of N₂O was observed in the cropland soil, also in sterilized samples. Correlation analysis revealed soil parameters that might explain the variability of NH₂OH-induced N₂O production to be: soil pH, C/N ratio, and Mn content. Our results suggest a coupled biotic–abiotic production of N₂O during nitrification, e.g. due to leakage of the nitrification intermediate NH₂OH with subsequent reaction with the soil matrix.     

Cropland age from grassland conversion to cropland affects nitrous oxide emissions

The effects of soil properties and cropland age on atmospheric nitrous oxide (N₂O) emissions following the conversion of grassland to cropland in temperate grassland ecosystems are uncertain. In this study, N₂O emissions were compared among grassland and cropland soils in the agro-pastoral ecotone of Inner Mongolia over three growing seasons. Four adjacent sites with different land-use histories were selected, including grassland and croplands cultivated for 5, 10, and 50 years after conversion. N₂O flux measurements were obtained using a closed-chamber method and were performed continuously during vegetation periods. After the conversion of grassland to cropland, N₂O emission initially decreased and thereafter increased in the study sites. The cumulative N₂O emissions of the cropland soils 5 and 10 years in age were 10–50% less than those of the grassland, and the N₂O emissions from the cropland soil 50 years in age were 10–30% greater than the grassland. When the seasonal emissions were correlated against single soil parameter, the key soil parameter that affected N₂O emissions over the entire growing season was the soil moisture content. When the interactions among soil parameters were considered, the amount of N₂O emissions could be quantitatively described by a linear combination of two soil variables, the soil ammonium nitrogen (NH₄⁺-N) and moisture concentrations. This study demonstrates how the time of land use conversion from grassland to cropland can positively or negatively affect N₂O emission.     

Ammonia volatilization following surface application of urea to tilled and no-till soils: A laboratory comparison

Broadcasting of urea to agricultural soils can result in considerable losses by NH₃ volatilization. However, it is unclear if the impact of this practice on NH₃ emissions is further enhanced when performed on no-till (NT) soils. The objective of this study was to compare NH₃ volatilization following broadcasting of urea to NT and moldboard plowed (MP) soils. Intact soil cores were taken shortly after harvest from NT and MP plots of three long-term tillage experiments in Québec (Canada) and stored for 4.5 months prior to incubation. Urea (14 g N m⁻²) was applied at the soil surface and NH₃ volatilization was measured for 30 d using an open incubation system. Mean cumulative NH₃ losses were greater (P < 0.001) in NT (3.00 g N m⁻²) than in MP (0.52 g N m⁻²). Several factors may have contributed to the higher emissions from the NT soils. Urease activity in the top 1 cm of soils was on average 4.2 times higher in NT than in MP soils. As a result, hydrolysis of urea occurred very rapidly in NT soils as indicated by enhanced NH₃ emissions 4 h after application of urea. The presence of crop residues at the surface of NT soils also decreased contact of the urea granules with the soil, possibly reducing adsorption of NH₄⁺ on soil particles. Lower volatilization on the MP soils may also have partly resulted from a fraction of urea granules falling into shallow cracks. Field trials are needed to confirm our finding that NT soils bear greater potential for NH₃ volatilization following surface application of urea than MP soils.     

Long-term large N and immediate small N addition effects on trace gas fluxes in the Colorado shortgrass steppe

 Land use changes in semiarid grasslands have long-lasting effects. Reversion to near-original conditions with respect to plant populations and productivity requires more than 50 years following plowing. The impact of more subtle management changes like small, annual applications of N fertilizer or changing cattle stocking rates, which alters N redistribution caused by grazing and cattle urine deposition, is not known. To investigate the long-term effects of N addition to the Colorado shortgrass steppe we made weekly, year-round measurements of N₂O and CH₄ from the spring of 1990 through June 1996. Fluxes of NO_x (NO plus NO₂) were measured from October 1995 through June 1996. These measurements illustrated that large N applications, either in a single dose (45 g N m^–2), simulating cattle urine deposition, or in small annual applications over a 15-year period (30 g N m^–2) continued to stimulate N₂O emissions from both sandy loam and clay loam soils 6–15 years after N application. In sandy loam soils last fertilized 6 years earlier, average NO_x emissions were 60% greater than those from a comparable, unfertilized site. The long-term impact of these N additions on CH₄ uptake was soil-dependent, with CH₄ uptake decreased by N addition only in the coarser textured soils. The short-term impact of small N additions (0.5–2 g N m^–2) on N₂O, NO_x emissions and CH₄ uptake was observed in field studies made during the summer of 1996. There was little short-term effect of N addition on CH₄ uptake in either sandy loam or clay loam soils. Small N additions did not result in an immediate increase in N₂O emissions from the sandy loam soil, but did significantly increase N₂O flux from the clay loam soil. The reverse soil type, N addition interaction occurred for NO_x emissions where N addition increased NO_x emissions in the coarser textured soil 10–20 times those of N₂O. Received: 31 October 1997     

Effect of urease and nitrification inhibitors on N transformation, gaseous emissions of ammonia and nitrous oxide, pasture yield and N uptake in grazed pasture system

Nitrogen (N) losses via nitrate (NO₃⁻) leaching, ammonia (NH₃) volatilization and nitrous oxide (N₂O) emissions from grazed pastures in New Zealand are one of the major contributors to environmental degradation. The use of N inhibitors (urease and nitrification inhibitors) may have a role in mitigating these N losses. A one-year field experiment was conducted on a permanent dairy-grazed pasture site at Massey University, Palmerston North, New Zealand to quantify these N losses and to assess the effect of N inhibitors in reducing such losses during May 2005-2006. Cow urine at 600 kg N ha⁻¹ rate with or without urease inhibitor N-(n-butyl) thiophosphoric triamide (nBTPT) or (trade name “Agrotain”) (3 L ha⁻¹), nitrification inhibitor dicyandiamide (DCD) (7 kg ha⁻¹) and the use of double inhibitor (DI) containing a combination of both Agrotain and DCD (3:7) were applied to field plots in autumn, spring and summer. Pasture production, NH₃ and N₂O fluxes, soil mineral N concentrations, microbial biomass C and N, and soil pH were measured following the application of treatments during each season. All measured parameters, except soil microbial biomass C and N, were influenced by the added inhibitors during the three seasons. Agrotain reduced NH₃ emissions over urine alone by 29%, 93% and 31% in autumn, spring and summer respectively but had little effect on N₂O emission. DCD reduced N₂O emission over urine alone by 52%, 39% and 16% in autumn, spring and summer respectively but increased NH₃ emission by 56%, 9% and 17% over urine alone during those three seasons. The double inhibitor reduced NH₃ by 14%, 78% and 9% and N₂O emissions by 37%, 67% and 28% over urine alone in autumn, spring and summer respectively. The double inhibitor also increased pasture dry matter by 10%, 11% and 8% and N uptake by the 17%, 28% and 10% over urine alone during autumn, spring and summer respectively. Changes in soil mineral N and pH suggested a delay in urine-N hydrolysis with Agrotain, and reduced nitrification with DCD. The combination of Agrotain and DCD was more effective in reducing both NH₃ and N₂O emissions, improving pasture production, controlling urea hydrolysis and retaining N in NH₄⁺ form. These results suggest that the combination of both urease and nitrification inhibitors may have the most potential to reduce N losses if losses are associated with urine and improve pasture production in intensively grazed systems.     

NH3 Volatilization,N2O Emission and Microbial Biomass Turnover from 15N-Labeled Manure Under Laboratory Conditions

On irrigated agricultural soils from semi-arid and arid regions, ammonia (NH₃) volatilization and nitrous oxide (N₂O) emission can be a considerable source of N losses. This study was designed to test the capture of ¹⁵N loss as NH₃ and N₂O from previous and recent manure application using a sandy, calcareous soil from Oman amended one or two times with ¹⁵N labeled manure to elucidate microbial turnover processes under laboratory conditions. The system allowed to detect ¹⁵N enrichments in evolved N₂O-N and NH₃-N of up to 17% and 9%, respectively, and total N, K₂SO₄ extractable N and microbial N pools from previous and recent ¹⁵N labeled manure applications of up to 7%, 8%, and 15%. One time manured soil had higher cumulative N₂O-N emissions (141 µg kg^?1) than repeatedly manured soil with 43 µg kg^?1 of which only 22% derived from recent manure application indicating a priming effect.     

Nitrous oxide emissions from animal urine application on a New Zealand pasture

Animal excreta-nitrogen (N) deposited onto pastoral soils during grazing has been identified as an important source of nitrous oxide (N₂O). Understanding the extent and seasonal variation of N₂O emissions from animal urine is important for the development of best management practices for reducing N₂O losses. The aim of this study was to determine N₂O emissions from cow urine after application onto a pastoral soil in different seasons between 2003 and 2005. A closed soil chamber technique was used to measure the N₂O emissions from a poorly drained silt loam soil which received either 0 (control) or 1,000 kg N ha⁻¹ (as real cow urine) per application. Application of cow urine to soil increased N₂O fluxes above those from the control site for up to 6 weeks, but the duration for which N₂O levels were elevated depended on the season. Nitrous oxide emissions were higher during the winter and spring measurement periods when the soil water-filled pore space (WFPS) was mostly above field capacity, and the emissions were lower during the summer and autumn measurement periods when the soil WFPS was below field capacity. The N₂O emission factor for urine ranged from 0.02 to 1.52% of N applied. This seasonal effect suggests that a reduction in urine return to soil (e.g., through use of standoff pads or animal housing) under wet conditions in New Zealand can potentially reduce N₂O emissions from pastoral soils.     

Reduction in Ammonia Loss by Applying Urea in Combination with Phosphate Sources

A laboratory experiment was carried out to study the influence of 100 mg phosphorus pentoxide (P₂O₅) kg^–1 soil from various phosphate sources on ammonia losses from soils amended with urea at 200 mg nitrogen (N) kg^–1 soil. Irrespective of soil type, ammonia (NH₃) loss was significantly greater from untreated soil (control) than from the soil treated with phosphorus (P) sources. A maximum decrease in ammonia loss (56%) was observed by applying phosphoric acid followed by triple and single superphosphate. Ammonia losses were significantly greater from sandy clay loam than from clay. Rate of ammonia volatilization was maximum during the first week of incubation and became undetectable for both soils at 21 days after incubation. The addition of phosphate sources significantly decreased pH in the sandy clay loam, but in the clay a significant decrease was observed only with the phosphoric acid addition. Addition of phosphate fertilizers was beneficial in reducing NH₃ losses from urea.