The influence of soluble carbon and fertilizer nitrogen on nitric oxide and nitrous oxide emissions from two contrasting agricultural soils

Contradictory effects of simultaneous available organic C and N sources on nitrous oxide (N₂O), carbon dioxide (CO₂) and nitric oxide (NO) fluxes are reported in the literature. In order to clarify this controversy, laboratory experiments were conduced on two different soils, a semiarid arable soil from Spain (soil I, pH=7.5, 0.8%C) and a grassland soil from Scotland (soil II, pH=5.5, 4.1%C). Soils were incubated at two different moisture contents, at a water filled pore space (WFPS) of 90% and 40%. Ammonium sulphate, added at rates equivalent to 200 and 50 kg N ha^?1, stimulated N₂O and NO emissions in both soils. Under wet conditions (90% WFPS), at high and low rates of N additions, cumulative N₂O emissions increased by 250.7 and 8.1 ng N₂O–N g^?1 in comparison to the control, respectively, in soil I and by 472.2 and 2.1 ng N₂O–N g^?1, respectively, in soil II. NO emissions only significantly increased in soil I at the high N application rate with and without glucose addition and at both 40% and 90% WFPS. In both soils additions of glucose together with the high N application rate (200 kg N ha^?1) reduced cumulative N₂O and NO emissions by 94% and 55% in soil I, and by 46% and 66% in soil II, respectively. These differences can be explained by differences in soil properties, including pH, soil mineral N and total and dissolved organic carbon content. It is speculated that nitrifier denitrification was the main source of NO and N₂O in the C-poor Spanish soil, and coupled nitrification–denitrification in the C-rich Scottish soil.     

Plant material addition affects soil nitrous oxide production differently between aerobic and oxygen-limited conditions

It is a common agricultural practice for crop residues to be plowed into the soil or left on the soil surface. Soil addition of crop residues can considerably modify soil microbial activity and net N mineralization, and in general such modifications are negatively related to the C:N ratios of crop residues. Yet, little is known on the impacts of crop residues of different C:N ratios on soil nitrous oxide (N₂O) production under different aeration conditions via nitrification and denitrification. In this study, an 84-day laboratory incubation was conducted under aerobic and O₂-limited conditions and soil N₂O production was measured every 3 days after the addition of plant materials with a wide range of C:N ratios from 14 to 297. Two aerobic conditions were created by adjusting the water content of soil at a bulk density of 1.1 g cm⁻³ to 30% water-filled pore space (WFPS) and 60% WFPS, and two O₂-limited conditions were made by 90% WFPS and fluctuation between 90% and 30% WFPS. Each fluctuation cycle lasted 9 days and soil water content was readjusted to 90% WFPS at the end of each cycle. We also measured microbial respiration activity and net N mineralization periodically (i.e., 3, 7, 14, 28, 42, 56, 70, and 84 days) during the incubation and microbial biomass C at the end of incubation. At aerobic conditions, soil amendments of plant materials, regardless of their C:N ratios, all enhanced soil N₂O production. However, net N mineralization was dependent on plant material C:N ratios, being significantly higher or lower than the control for C:N ratios ∼15 and C:N ratios ≥44, respectively. Such inconsistent responses indicated that nitrifiers mediating nitrification and therefore byproduct N₂O production could strongly compete with heterotrophic microbes for NH₄⁺ and therefore net N mineralization was not a good predictor for nitrification-associated N₂O production. Interestingly, plant material additions reduced soil N₂O production by up to ∼95% at O₂-limited conditions, perhaps due to NO₃⁻ limitation. Soil NO₃⁻ production via nitrification could be low at O₂-limited conditions, and soil NO₃⁻ availability could be further reduced due to increases in microbial biomass and thus microbial N assimilation after plant material additions. This NO₃⁻ limitation might enhance N₂O reduction to N₂, by which denitrifiers could harvest more energy from the consumption of limited NO₃⁻. Nonetheless, our results revealed contrasting differences in N₂O production between aerobic and O₂-limited conditions following soil amendments of plant materials.     

Earthworm-induced N2O emissions in a sandy soil with surface-applied crop residues

Earlier research with endogeic and epigeic earthworm species in loamy arable soil has shown that both earthworm groups can increase nitrous oxide (N₂O) emissions, provided that crop residue placement matches the feeding strategy of the earthworm ecological group(s). However, it is not yet clear whether these effects also occur in sandy soils which typically contain less soil organic matter and have low soil aggregation levels. Here, we aimed to quantify N₂O emissions as affected by endogeic and/or epigeic earthworm species, and to relate changes in N₂O emissions to earthworm-induced changes in soil properties in a sandy soil. A 90 day mesocosm study was conducted with sandy soil and ¹⁵N-labeled radish (Raphanus sativus cv. Adagio L.) residue applied on top. Treatments included: (i) no earthworm addition, (ii) addition of the endogeic species Aporrectodea caliginosa (Savigny), (iii) addition of the epigeic species Lumbricus rubellus (Hoffmeister), and (iv) both species combined. An additional treatment was included without earthworms and with residue manually incorporated into the soil. L. rubellus significantly increased cumulative N₂O emissions from 228 to 859 μg N₂O–N kg^?1 (F_1,12 = 83.12, P < 0.001), whereas A. caliginosa did not affect N₂O emissions. In contrast to earlier studies in loamy soil, no positive interaction between both species with regard to N₂O emissions was found. This was probably related to high competition for organic resources in the relatively poor soil and a low potential for stable soil aggregate formation (and associated anaerobic microsites) by endogeic worms in sandy soil. ¹⁵N isotope analysis revealed that the activity of L. rubellus significantly increased (F_1,12 = 6.20, P = 0.028) the recovery of ¹⁵N in the 250–8000 μm size fraction, indicating incorporation of crop residues into the mineral soil. When residues were manually incorporated, N₂O emissions were significantly (P < 0.008) lower (509 μg N₂O–N kg^?1) than when incorporated by L. rubellus. The high N₂O emissions in the presence of L. rubellus, when compared to manual mixing, suggest a stimulation of microbial activity and/or changes in the microbial community composition. Insights on the earthworm effects on N₂O emission from such soils are discussed.     

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.     

Emission of nitrous oxide from hydrocarbon contaminated soil amended with waste water sludge and earthworms

Soils in Mexico are often contaminated with hydrocarbons and addition of waste water sludge and earthworms accelerates their removal. However, little is known how contamination and subsequent bioremediation affects emissions of N₂O and CO₂. A laboratory study was done to investigate the effect of waste water sludge and the earthworm Eisenia fetida on emission of N₂O and CO₂ in a sandy loam soil contaminated with the polycyclic aromatic hydrocarbons (PAHs): phenanthrene, anthracene and benzo(a)pyrene. Emissions of N₂O and CO₂, and concentrations of inorganic N (ammonium (NH₄⁺), nitrite (NO₂^?) nitrate (NO₃^?)) were monitored after 0, 5, 24, 72 and 168 h. Adding E. fetida to the PAHs contaminated soil increased CO₂ production rate significantly 2.0 times independent of the addition of sludge. The N₂O emission rate from unamended soil expressed on a daily base was 5 μg N kg^?1 d^?1 for the first 2 h and increased to a maximum of 325 μg N kg^?1 d^?1 after 48 h and then decreased to 10 μg N kg^?1 d^?1 after 168 h. Addition of PAHs, E. fetida or PAHs + E. fetida had no significant effect on the N₂O emission rate. Adding sludge to the soil sharply increased the N₂O emission rate to >400 μg N kg^?1 d^?1 for the entire incubation with a maximum of 1134 μg N kg^?1 d^?1 after 48 h. Addition of E. fetida, PAHs or PAHs + E. fetida to the sludge-amended soil reduced the N₂O emission rate significantly compared to soil amended with sludge after 24 h. It was found that contaminating soil with PAHs and adding earthworms had no effect on emissions of N₂O. Emission of N₂O, however, increased in sludge-amended soil, but addition of earthworms to this soil and contamination reduced it.     

Soil–atmosphere greenhouse gas exchange in a cool,temperate Eucalyptus delegatensis forest in south-eastern Australia

Forests are the largest C sink (vegetation and soil) in the terrestrial biosphere and may additionally provide an important soil methane (CH₄) sink, whilst producing little nitrous oxide (N₂O) when nutrients are tightly cycled. In this study, we determine the magnitude and spatial variation of soil–atmosphere N₂O, CH₄ and CO₂ exchange in a Eucalyptus delegatensis forest in New South Wales, Australia, and investigate how the magnitude of the fluxes depends on the presence of N₂-fixing tree species (Acacia dealbata), the proximity of creeks, and changing environmental conditions. Soil trace gas exchange was measured along replicated transects and in forest plots with and without presence of A. dealbata using static manual chambers and an automated trace gas measurement system for 2 weeks next to an eddy covariance tower measuring net ecosystem CO₂ exchange. CH₄ was taken up by the forest soil (?51.8 μg CH₄-C m^?2 h^?1) and was significantly correlated with relative saturation (S_r) of the soil. The soil within creek lines was a net CH₄ source (up to 33.5 μg CH₄-C m^?2 h^?1), whereas the wider forest soil was a CH₄ sink regardless of distance from the creek line. Soil N₂O emissions were small (<3.3 μg N₂O-N m^?2 h^?1) throughout the 2-week period, despite major rain and snowfall. Soil N₂O emissions only correlated with soil and air temperature. The presence of A. dealbata in the understorey had no influence on the magnitude of CH₄ uptake, N₂O emission or soil N parameters. N₂O production increased with increasing soil moisture (up to 50% S_r) in laboratory incubations and gross nitrification was negative or negligible as measured through ¹⁵N isotope pool dilution.The small N₂O emissions are probably due to the limited capacity for nitrification in this late successional forest soil with C:N ratios >20. Soil–atmosphere exchange of CO₂ was several orders of magnitude greater (88.8 mg CO₂-C m^?2 h^?1) than CH₄ and N₂O, and represented 43% of total ecosystem respiration. The forest was a net greenhouse gas sink (126.22 kg CO₂-equivalents ha^?1 d^?1) during the 2-week measurement period, of which soil CH₄ uptake contributed only 0.3% and N₂O emissions offset only 0.3%.     

Nitrous oxide emissions from fertilized,irrigated cotton (Gossypium hirsutum L.) in the Aral Sea Basin,Uzbekistan: Influence of nitrogen applications and irrigation practices

Nitrous oxide emissions were monitored at three sites over a 2-year period in irrigated cotton fields in Khorezm, Uzbekistan, a region located in the arid deserts of the Aral Sea Basin. The fields were managed using different fertilizer management strategies and irrigation water regimes. N₂O emissions varied widely between years, within 1 year throughout the vegetation season, and between the sites. The amount of irrigation water applied, the amount and type of N fertilizer used, and topsoil temperature had the greatest effect on these emissions.Very high N₂O emissions of up to 3000 μg N₂O-N m^?2 h^?1 were measured in periods following N-fertilizer application in combination with irrigation events. These “emission pulses” accounted for 80–95% of the total N₂O emissions between April and September and varied from 0.9 to 6.5 kg N₂O-N ha^?1.. Emission factors (EF), uncorrected for background emission, ranged from 0.4% to 2.6% of total N applied, corresponding to an average EF of 1.48% of applied N fertilizer lost as N₂O-N. This is in line with the default global average value of 1.25% of applied N used in calculations of N₂O emissions by the Intergovernmental Panel on Climate Change.During the emission pulses, which were triggered by high soil moisture and high availability of mineral N, a clear diurnal pattern of N₂O emissions was observed, driven by daily changes in topsoil temperature. For these periods, air sampling from 8:00 to 10:00 and from 18:00 to 20:00 was found to best represent the mean daily N₂O flux rates. The wet topsoil conditions caused by irrigation favored the production of N₂O from NO₃^? fertilizers, but not from NH₄⁺ fertilizers, thus indicating that denitrification was the main process causing N₂O emissions. It is therefore argued that there is scope for reducing N₂O emission from irrigated cotton production; i.e. through the exclusive use of NH₄⁺ fertilizers. Advanced application and irrigation techniques such as subsurface fertilizer application, drip irrigation and fertigation may also minimize N₂O emission from this regionally dominant agro-ecosystem.     

Incongruous variation of denitrifying bacterial communities as soil N level rises in Canadian canola fields

Soil N fertilization stimulates the activity of the soil bacterial species specialized in performing the different steps of the denitrification processes. Different responses of these bacterial denitrifiers to soil N management could alter the efficiency of reduction of the greenhouse gas N₂O into N₂ gas in cultivated fields. We used next generation sequencing to show how raising the soil N fertility of Canadian canola fields differentially modifies the diversity and composition of nitrite reductase (nirK and nirS) and nitrous oxide reductase (nosZ) gene-carrying denitrifying bacterial communities, based on a randomized complete blocks field experiment. Raising soil N levels increased up to 60% the ratio of the nirK to nirS genes, the two nitrite reductase coding genes, in the Brown soil and up to 300% in the Black soil, but this ratio was unaffected in the Dark Brown soil. Raising soil N levels also increased the diversity of the bacteria carrying the nitrite reductase gene nirK (Simpson index, P = 0.0417 and Shannon index, 0.0181), and changed the proportions of the six dominant phyla hosting nirK, nirS, and nosZ gene-carrying bacteria. The level of soil copper (Cu) and the abundance of nirK gene, which codes for a Cu-dependent nitrite reductase, were positively related in the Brown (P = 0.0060, R² = 0.48) and Dark Brown (0.0199, R² = 0.59) soils, but not in the Black soil. The level of total diversity of the denitrifying communities tended to remain constant as N fertilization induced shifts in the composition of these denitrifying communities. Together, our results indicate that higher N fertilizer rate increases the potential risk of nitrous oxide (N₂O) emission from canola fields by promoting the proliferation of the mostly adaptive N₂O-producing over the less adaptive N₂O-reducing bacterial community.     

Small-scale heterogeneity in carbon dioxide, nitrous oxide and methane production from aggregates of a cultivated sandy-loam soil

Spatial variability in carbon dioxide (CO₂), nitrous oxide (N₂O) and methane (CH₄) emissions from soil is related to the distribution of microsites where these gases are produced. Porous soil aggregates may possess aerobic and anaerobic microsites, depending on the water content of pores. The purpose of this study was to determine how production of CO₂, N₂O and CH₄ was affected by aggregate size and soil water content. An air-dry sandy loam soil was sieved to generate three aggregate fractions (<0.25 mm, 0.25–2 mm and 2–6 mm) and bulk soil (<2 mm). Aggregate fractions and bulk soil were moistened (60% water-filled pore space, WFPS) and pre-incubated to restore microbial activity, then gradually dried or moistened to 20%, 40%, 60% or 80% WFPS and incubated at 25 °C for 48 h. Soil respiration peaked at 40% WFPS, presumably because this was the optimum level for heterotrophic microorganisms, and at 80% WFPS, which corresponded to the peak N₂O production. More CO₂ was produced by microaggregates (<0.25 mm) than macroaggregate (>0.25 mm) fractions. Incubation of aggregate fractions and soil at 80% WFPS with acetylene (10 Pa and 10 kPa) and without acetylene showed that denitrification was responsible for 95% of N₂O production from microaggregates, while nitrification accounted for 97–99% of the N₂O produced by macroaggregates and bulk soil. This suggests that oxygen (O₂) diffusion into and around microaggregates was constrained, whereas macroaggregates remained aerobic at 80% WFPS. Methane consumption and production were measured in aggregates, reaching 1.1–6.4 ng CH₄–C kg⁻¹ soil h⁻¹ as aggregate fractions and soil became wetter. For the sandy-loam soil studied, we conclude that nitrification in aerobic microsites contributed importantly to total N₂O production, even when the soil water content permitted denitrification and CH₄ production in anaerobic microsites. The relevance of these findings to microbial processes controlling N₂O production at the field scale remains to be confirmed.     

Pig slurry treatment modifies slurry composition,N2O,and CO2 emissions after soil incorporation

The treatment of manures may improve their agricultural value and environmental quality, for instance with regards to greenhouse gases mitigation and enhancement of carbon (C) sequestration. The present study verified whether different pig slurry treatments (i.e. solid/liquid separation and anaerobic digestion) changed slurry composition. The effect of the slurry composition on N₂O and CO₂ emissions, denitrification and soil mineral nitrogen (N), after soil incorporation, was also examined during a 58-day mesocosm study. The treatments included a non-treated pig slurry (NT), the solid fraction (SF), and the liquid fraction (LF) of a pig slurry and the anaerobically digested liquid fraction (DG). Finally, a non-fertilized (N0) and a treatment with urea (UR) were also present.The N₂O emissions measured represented 4.8%, 2.6%, 1.8%, 1.0% and 0.9% of N supplied with slurry/fertilizer for NT, LF, DG, SF and UR, respectively. Cumulative CO₂ emissions ranged from 0.40 g CO₂-C kg^?1 soil (0.38 Mg CO₂-C ha^?1) to 0.80 g CO₂-C kg^?1 soil (0.75 Mg CO₂-C ha^?1). They were highest for SF (56% of C applied), followed by NT (189% of C applied), LF (337% of C applied) and DG (321% of C applied). Ammonium was detected in the soil for all treatments only at day one, while nitrate concentration increased linearly from day 15 to day 58, at a rate independent of the type of slurry/fertilizer applied. The nitrate recovery at day 58 was 39% of the N applied for NT, 19% for SF, 52% for LF, 67% for DG, and 41% for UR. The solid fraction generally produced higher potential denitrification fluxes (75.3 for SF, 56.7 for NT, 53.6 for LF, 47.7 for DG and 39.7 mg N₂O + N₂-N kg^?1 soil for UR). The high variability of actual denitrification results obfuscated any treatment effect.We conclude that treatment strongly affects slurry composition (mainly its C, fibre and NH₄⁺ content), and hence N₂O and CO₂ emission patterns as well as denitrification processes and nitrate availability. In particular, the solid fraction obtained after mechanical separation produced the most pronounced difference, while the liquid fraction and the anaerobically digested liquid fraction did not show significant difference with respect to the original slurry for any of the measured parameters. Combining data from the different fractions we showed that separation of slurry leads to reduced N₂O emissions, irrespective of whether the liquid fraction is digested or not. Furthermore, our results suggested that the default emission factor for N₂O emissions inventory is too low for both the non-treated pig slurry and its liquid fraction (digested or not), and too high for the separated solid fraction and urea.     

In-field management of corn cob and residue mix: Effect on soil greenhouse gas emissions

In-field management practices of corn cob and residue mix (CRM) as a feedstock source for ethanol production can have potential effects on soil greenhouse gas (GHG) emissions. The objective of this study was to investigate the effects of CRM piles, storage in-field, and subsequent removal on soil CO₂ and N₂O emissions. The study was conducted in 2010–2012 at the Iowa State University, Agronomy Research Farm located near Ames, Iowa (42.0°′N; 93.8°′W). The soil type at the site is Canisteo silty clay loam (fine-loamy, mixed, superactive, calcareous, mesic Typic Endoaquolls). The treatments for CRM consisted of control (no CRM applied and no residue removed after harvest), early spring complete removal (CR) of CRM after application of 7.5 cm depth of CRM in the fall, 2.5 cm, and 7.5 cm depth of CRM over two tillage systems of no-till (NT) and conventional tillage (CT) and three N rates (0, 180, and 270 kg N ha⁻¹) of 32% liquid UAN (NH₄NO₃) in a randomized complete block design with split–split arrangements. The findings of the study suggest that soil CO₂ and N₂O emissions were affected by tillage, CRM treatments, and N rates. Most N₂O and CO₂ emissions peaks occurred as soil moisture or temperature increased with increase precipitation or air temperature. However, soil CO₂ emissions were increased as the CRM amount increased. On the other hand, soil N₂O emissions increased with high level of CRM as N rate increased. Also, it was observed that NT with 7.5 cm CRM produced higher CO₂ emissions in drought condition as compared to CT. Additionally, no differences in N₂O emissions were observed due to tillage system. In general, dry soil conditions caused a reduction in both CO₂ and N₂O emissions across all tillage, CRM treatments, and N rates.     

Emergence and behaviors of acid-tolerant Janthinobacterium sp. that evolves N2O from deforested tropical peatland

Using a soilless culture system mimicking tropical acidic peat soils, which contained 3 mg of gellan gum and 0.5 mg NO₃^?-N per gram of medium, a greenhouse gas, N₂O emitting capability of microorganisms in acidic peat soil in the area of Palangkaraya, Central Kalimantan, Indonesia, was investigated. The soil sampling sites included a native swamp forest (NF), a burnt forest covered by ferns and shrubs (BF), three arable lands (A-1, A-2 and A-3) and a reclaimed grassland (GL) next to the arable lands. An acid-tolerant Janthinobacterium sp. strain A1-13 (Oxalobacteriaceae, β-proteobacteria) isolated from A-1 soil was characterized as one of the most prominent N₂O-emitting bacteria in this region. Physiological characteristics of the N₂O emitter in the soilless culture system, including responses to soil environments, substrate concentration, C-source concentration, pH, and temperature, suggest that the N₂O emitting Janthinobacterium sp. strain A1-13 is highly adapted to reclaimed open peatland and primarily responsible for massive N₂O emissions from the acidic peat soils. Regulation of N₂O emitters in the reclaimed peatland for agricultural use is therefore one of the most important issues in preventing the greenhouse gas emission from acidic peat soil farmlands.     

Effects of alternative management practices on the economics,energy and GHG emissions of a wheat–pea cropping system in the Canadian prairies

In recent years alternative farming practices have received considerable attention from Canadian producers as a means to improve their net return from grain and oilseed production. Enhancing the efficiency of nitrogen fertilizer use, including a pulse crop in the rotation, reducing tillage and pesticide use are seen as viable options to reduce reliance on fossil fuel, lower input costs and decrease the risk of soil, air and water degradation. The objective of this study was to determine the effects of 16 alternative management practices for a 2-year spring wheat (Triticum aestivum L.)–field pea (Pisum sativum L.) rotation on economic returns, non-renewable energy use efficiency, and greenhouse gas emissions. The alternative management methods for wheat consisted of a factorial combination of high vs. low soil disturbance one pass seeding, four nitrogen (N) fertilizer rates (20 kg N ha^?1, 40 kg N ha^?1, 60 kg N ha^?1 and 80 kg N ha^?1), and recommended vs. reduced rates of in-crop herbicide application. Alternative management practices for field pea were high vs. low soil disturbance one pass seeding. The resulting 16 cropping systems were evaluated at the whole farm level based on 4 years (two rotation cycles) of data from field experiments conducted on two Orthic Black Chernozem soils (clay loam and loam textures) in Manitoba, Canada. The highest net returns on the clay loam soil were for the high disturbance system with 60 kg N ha^?1 applied to wheat and the recommended rates of in-crop herbicides. The lowest application rate of N, together with low disturbance seeding, provided the highest economic returns on the loam soil. Energy use efficiency was highest for the lowest rate of N application for both tillage systems. The highest rate of N fertilizer and recommended rates of in-crop herbicide produced little additional yield response, lower net returns, and higher GHG emissions. An increase in N fertilizer application from 20 kg ha^?1 to 80 kg ha^?1 increased whole farm energy requirements by about 40%, while reducing herbicide rates had negligible effects on grain yields and total energy input. Overall, as N fertilizer rate increased, the associated GHG emissions were not offset by an increase in carbon retained in the above-ground crop biomass. Moderate to high soil test NO₃-N levels at experimental sites reduced the potential for positive yield responses to N fertilizer in this study, thus minimizing the economic benefits derived from N fertilizer application.     

Effect of wetting intensity on soil GHG fluxes and microbial biomass under a temperate forest floor during dry season

The increasing frequency of periodic droughts followed by heavy rainfalls is expected for this current century, but little is known about the effects of wetting intensity on the in situ biogenic greenhouse gas (GHG) fluxes of forest soils and soil microbial biomass. To gain new insights into the underlying mechanisms responsible for wetting-induced GHG fluxes in situ, rain simulation field experiments during a natural prolonged drought period were done under a temperate forest in northeast China. The intensity of rainfall-induced CO₂ pulses increased from 0.84 to 2.08 g CO₂–C m^? 2 d^? 1 with the intensity of wetting up to ca. 80% water-filled pore space, which coincided with an increase in soil microbial biomass and with a decrease in soil labile organic C following wetting. Methane uptake rates decreased from 1.76 to 0.87 mg CH₄–C m^? 2 d^? 1 with the intensity of wetting. Wetting dry forest floor increased N₂O fluxes from 6.2 to 25.9 μg N₂O–N m^? 2 d^? 1, but there was no significant difference between all experimental wetted plots. The rainfall-induced N₂O pulses with increasing wetting intensity were opposite to that of the CO₂ pulses, showing a maximum response at the lowest wetting intensity. An analysis of the temperature sensitivity of GHG fluxes indicated that temperature had an increased effect on the in situ CO₂ flux and CH₄ uptake, respectively, under wetted and dry conditions. The global warming potential of GHG fluxes and Q₁₀ value of the temperature response of CO₂ fluxes increased linearly with wetting intensity. The results indicate that the rainfall-induced soil CO₂ pulse is mainly due to enhanced microbial consumption on substrates and highlight the complex nature of belowground C-cycling responses to climate change in northeast China forests that normally experience periodic droughts followed by heavy rainfalls over the year.     

Production of carbon dioxide and nitrous oxide in alkaline saline soil of Texcoco at different water contents amended with urea: A laboratory study

Soil of the former lake Texcoco is alkaline saline with pH often >10 and electrolytic conductivity (EC) >70 dS m^?1 with rapidly changing water contents. Little is known how fertilizing this area with urea to vegetate the soil would affect emissions of carbon dioxide (CO₂) and dynamics of N. Texcoco soil with electrolytic conductivity (EC) 2.3 dS m^?1 and pH 8.5 (TEXCOCO A soil), EC 2.0 dS m^?1 and pH 9.0 (TEXCOCO B soil) and 200 dS m^?1 and pH 11.2 (TEXCOCO C soil) was amended with or without urea and incubated at 40% of water holding capacity (WHC), 60% WHC, 80% WHC and 100% WHC, while emissions of nitrous oxide (N₂O) and CO₂ and dynamics of ammonium (NH₄⁺), nitrite (NO₂^?) and nitrate (NO₃^?) were monitored for 7 days. An agricultural soil served as control (ACOLMAN soil). The emission of CO₂ increased in the urea amended soil 1.5 times compared to the unamended soil, it was inhibited in TEXCOCO C soil and was >1.2 larger in soil incubated at 40%, 60% and 80% WHC compared to soil incubated at 100% WHC. The emission of N₂O increased in soil added with urea compared to the unamended soil, was similar in TEXCOCO A and B soils, but was <0.2 mg N kg^?1 soil day^?1 in TEXCOCO C soil and generally larger in soil incubated at 60% and 80% WHC compared to soil incubated at 40% and 100% WHC. The water content of the soil had no significant effect on the mean concentration of NH₄⁺, but addition of urea increased it in all soils. The concentration of NO₂^? was not affected by the water content and the addition of urea except in TEXCOCO A soil where it increased to values ranging between 20 and 40 mg N kg^?1. The concentration of NO₃^? increased in the ACOLMAN, TEXCOCO A and TEXCOCO B soil amended with urea compared to the unamended soil, but not in the TEXCOCO C soil. It decreased with increased water content, but not in TEXCOCO C soil. It was found that the differences in soil characteristics, i.e. soil organic matter content, pH and EC between the soils had a profound effect on soil processes, but even small changes affected the dynamics of C and N in soil amended with urea.     

The temperature dependence of dicyandiamide (DCD) degradation in soils: A data synthesis

Dicyandiamide (DCD, C₂H₄N₄) is a nitrification inhibitor that has been studied for more than 80 years. However, there are few papers that have examined the use of DCD on dairy farms where cattle graze pasture and where urine is the primary form of nitrogen (N) deposited onto soils. After DCD was applied (10 kg DCD ha^?1) with bovine urine (700–1200 kg N ha^?1) to five soils throughout New Zealand, the reduction in direct nitrous oxide (N₂O) emissions was significant and remarkably consistent (71 ± 8%, average ± standard error). The application of DCD to these soils occurred in autumn and winter; daily average soil temperature (T) was reported but these data were not further analysed. Perusal of the literature suggested no consensus on the temperature dependence of DCD degradation in soils. Based on published data from controlled-environment studies of soils sampled in four countries, we quantified the relation between T and the time for DCD concentration in soils to decline to half its application value (t_½) as t_½ (T) = 168e^?0.084T with parameter standard errors of ±16 d and ±0.011 d^?1, respectively (n = 16). For example, at 5 °C a 1 °C increase in T reduced t_½ from 110 to 101 d whereas at 25 °C the reduction was 20–19 d. Analysing T data from the New Zealand trials using our t_½ (T) function, over 43–89 d when direct N₂O emissions from treated plots became indistinguishable from the controls, the estimated percentage of applied DCD remaining in the soil averaged 43 ± 10%. These calculations suggested the apparently remaining DCD was ineffective with respect to direct N₂O emissions. In the absence of measurements, explanations for this interpretation included vertical displacement of the DCD and sorption onto organic matter in soils. The consistent DCD efficacy from these trials corresponded with T generally <10 °C, so it is suggested as an application criteria for the reduction of direct N₂O emissions from pastoral soils subjected to urine excretion by grazing cattle.     

Nitrogen fertilization and cropping systems effects on soil organic carbon and total nitrogen pools under chisel-plow tillage in Illinois

Agricultural soils can be a major sink for atmospheric carbon (C) with adoption of recommended management practices (RMPs). Our objectives were to evaluate the effects of nitrogen (N) fertilization and cropping systems on soil organic carbon (SOC) and total N (TN) concentrations and pools. Replicated soil samples were collected in May 2004 to 90 cm depth from a 23-year-old experiment at the Northwestern Illinois Agricultural Research and Demonstration Center, Monmouth, IL. The SOC and TN concentrations and pools, soil bulk density (ρ_b) and soil C:N ratio were measured for five N rates [0 (N₀), 70 (N₁), 140 (N₂), 210 (N₃) and 280 (N₄) kg N ha⁻¹] and two cropping systems [continuous corn (Zea mays L.) (CC), and corn–soybean (Glycine max (L.) Merr.) rotation (CS)]. Long-term N fertilization and cropping systems significantly influenced SOC concentrations and pools to 30 cm depth. The SOC pool in 0–30 cm depth ranged from 68.4 Mg ha⁻¹ for N₀ to 75.8 Mg ha⁻¹ for N₄. Across all N treatments, the SOC pool in 0–30 cm depth for CC was 4.7 Mg ha⁻¹ greater than for CS. Similarly, TN concentrations and pools were also significantly affected by N rates. The TN pool for 0–30 cm depth ranged from 5.36 Mg ha⁻¹ for N₀ to 6.14 Mg ha⁻¹ for N₄. In relation to cropping systems, the TN pool for 0–20 cm depth for CC was 0.4 Mg ha⁻¹ greater than for CS. The increase in SOC and TN pools with higher N rates is attributed to the increased amount of biomass production in CC and CS systems. Increasing N rates significantly decreased ρ_b for 0–30 cm and decreased the soil C:N ratio for 0–10 cm soil depth. However, none of the measured soil properties were significantly correlated with N rates and cropping systems below 30 cm soil depth. We conclude that in the context of developing productive and environmentally sustainable agricultural systems on a site and soil specific basis, the results from this study is helpful to strengthening the database of management effects on SOC storage in the Mollisols of Midwestern U.S.     

Emissions of CH4, CO2, and N2O from soil at a cattle overwintering area as affected by available C and N

Relationships between CH₄, CO₂, and N₂O emissions were studied in soil that had been freshly amended with large deposits of cattle wastes. Dynamics of CH₄, CO₂, and N₂O emissions were investigated with flux chambers from early April to late June 2011, during the 3 months following cattle overwintering at the site. This 81-day field study was supplemented with soil analyses of available C and N content and measurement of denitrification activity. In a more detailed field investigation, the daily time course of emissions was determined. The field research was complemented with a laboratory experiment that focused on the short-term time course of N₂O and CH₄ production in artificially created anoxic soil microsites. The following hypotheses were tested: (i) a large input of C (and N and other nutrients) in cattle manure creates conditions suitable for methanogenesis, and therefore overwintering areas can produce large amounts of CH₄; (ii) N₂O is produced and emitted until the level of mineral N decreases, while the level of CH₄ production is low; and (iii) production of CH₄ is greater when N immobilization decreases the level of NO₃⁻ in soil. N₂O emissions were relatively large during the first 3 weeks, then peaked (at ca. 4000 μg N₂ON m⁻² h⁻¹) and soon decreased to almost zero; the changes were related to the mineral and soluble organic N content in soil. CH₄ fluxes were large, though variable, in the first 2 months (600–3000 μg CH₄C m⁻² h⁻¹) and were independent of C and N availability. Although time courses differed for CH₄ and N₂O, a negative relationship between N₂O and CH₄ emissions was not detected. Contrary to CH₄ and N₂O fluxes, CO₂ emissions progressively increased to ca. 300 mg CO₂C m⁻² h⁻¹ at the end of the field study and were closely related to air and soil temperatures. Diurnal measurements revealed significant correlations between temperature and emissions of CH₄, N₂O, and CO₂. Addition of C to soil during anaerobic incubation increased the production and consumption of N₂O and supported the emission of CH₄. The results suggest that rapid denitrification significantly contributes to the exhaustion of oxidizing agents and helps create microsites supporting methanogenesis in otherwise N₂O-producing upland soil. The results also indicate that accurate estimate of gas fluxes in animal-impacted grassland areas requires assessment of both diurnal and long-term changes in CH₄, CO₂, and N₂O emissions.     

Depth-specific distribution and importance of nitrite-dependent anaerobic ammonium and methane-oxidising bacteria in an urban wetland

Anaerobic ammonium oxidation (anammox) and nitrite-dependent anaerobic methane oxidation (n-damo) are two recently discovered processes in the nitrogen cycle that are catalysed by anammox bacteria and n-damo bacteria, respectively. Here, the depth-specific distribution and importance of anammox bacteria and n-damo bacteria were studied in an urban wetland, Xixi Wetland, Zhejiang Province (China). Anammox bacteria related to Candidatus Brocadia, Candidatus Kuenenia and Candidatus Anammoxoglobus, and n-damo bacteria related to “Candidatus Methylomirabilis oxyfera” were present in the collected soil samples. The abundance of anammox bacteria (2.6–8.6 × 10⁶ copies g⁻¹ dry soil) in the shallow soils (0–10 cm and 20–30 cm) was higher than that (2.5–9.8 × 10⁵ copies g⁻¹ dry soil) in the deep soils, whereas the abundance of n-damo bacteria (0.6–1.3 × 10⁷ copies g⁻¹ dry soil) in the deep soils (50–60 cm and 90–100 cm) was higher than that (3.4–4.5 × 10⁶ copies g⁻¹ dry soil) in the shallow soils. Anammox activity was detected at all depths, and higher potential rates (12.1–21.4 nmol N₂ g⁻¹ dry soil d⁻¹) were observed at depths of 0–10 cm and 20–30 cm compared with the rates (3.5–8.7 nmol N₂ g⁻¹ dry soil d⁻¹) measured at depths of 50–60 and 90–100 cm. In contrast, n-damo was mainly occurred at depths of 50–60 cm and 90–100 cm with potential rates of 0.7–5.0 nmol CO₂ g⁻¹ dry soil d⁻¹. This study suggested the niche segregation of the anammox bacteria and n-damo bacteria in wetland soils, with anammox bacteria being active primarily in deep soils and n-damo bacteria being active primarily in shallow soils.     

Sclerotium rolfsii dynamics in soil as affected by crop sequences

Crop rotation has been used for the management of soilborne diseases for centuries, but has not often been planned based on scientific knowledge. Our objective was to generate information on Sclerotium rolfsii dynamics under different crop or intercrop activities, and design and test a research approach where simple experiments and the use of models are combined to explore crop sequences that minimize Southern blight incidence.The effect of seventeen green manure (GM) amendments on sclerotia dynamics was analyzed in greenhouse and field plot experiments during two years. The relative densities of viable sclerotia 90 days after winter GM (WGM) incorporation were generally lower than after summer GM (SGM) incorporation, with average recovery values of 60% and 61% for WGM in the field, 66% and 43% for WGM in the greenhouse, and 162% to 91% for SGM in the greenhouse, in 2009 and 2010, respectively. Sclerotia survival on day d after GM amendment was described by the model S_f = S_i × exp(−b × d), relating initial (S_i) and final (S_f) sclerotia densities. Relative decay rates of the sclerotia (b) in SGM amended soil were largest for alfalfa (0.0077 ± 0.0031 day⁻¹) and sudangrass (0.0072 ± 0.0030 day⁻¹). In WGM amended soil, the largest b values were for oat (0.0096 ± 0.0024 day⁻¹), wheat (0.0090 ± 0.0024 day⁻¹) and alfalfa (0.0087 ± 0.0023 day⁻¹).The effect of three cropping sequences (sweet pepper–fallow, sweet pepper–black oat and sweet pepper–onion) on sclerotia dynamics was analyzed in microplot experiments, and the data were used to calibrate the model P_f = P_i/(α + βP_i), relating initial (P_i) and final (P_f) sclerotia densities. Median values for the relative rate of population increase at low P_i (1/α, dimension less) and the asymptote (1/β, number of viable sclerotia in 100 g of dry soil) were 8.22 and 4.17 for black oat (BO), 1.13 and 8.64 for onion (O), and 6.26 and 17.93 for sweet pepper (SwP).By concatenating the two models, sclerotia population dynamics under several crop sequences were simulated. At steady state, the sequence SwP–O–Fallow–BO resulted in the lowest long-term sclerotia density (7.09 sclerotia/100 g soil), and SwP–Fallow in the highest (17.89 sclerotia/100 g soil). The developed methodology facilitates the selection of a limited number of rotation options to be tested in farmers’ fields.