Soil nitrogen dynamics in irrigated maize systems as impacted on by nitrogen and stubble management

2008 ◽  
Vol 48 (3) ◽  
pp. 382 ◽  
Author(s):  
R. B. Edis ◽  
D. Chen ◽  
G. Wang ◽  
D. A. Turner ◽  
K. Park ◽  
...  

The soil nitrogen (N) dynamics of an irrigated maize system in which stubble retention and stubble burned treatments were superimposed over treatments of varying N fertiliser rate were studied. The field site was near Whitton, New South Wales, Australia, and the work described here is part a life cycle analysis of greenhouse gas emissions from maize project. The objective of this part of the work was to quantify the fate of fertiliser N applied at the site. Field measurements of denitrification, mineral N content and recovery of 15N-labelled urea from microplots with and without ammonium thiosulfate were complimented with laboratory studies of denitrification and nitrous oxide (N2O) flux. Significantly (P < 0.05) more fertiliser N was recovered in the grain from the stubble incorporated treatment than the stubble burned treatment and there was greater recovery of fertiliser N in the soil at the end of the experiment in the stubble burned treatment. This may indicate that fertiliser N applied to the stubble burned system may be more exposed to soil-N transformations. The reason for the difference in uptake and soil residual is not clear but may be related to soil structure differences leading to less plant accessibility of N in the burned treatment. This difference may lead to more nitrous oxide emission from soil in the stubble burned treatments. Short-term (1 h) static chamber measurements in the field found a strong N-rate dependence of N2O emission rate for fertiliser rates between 0 and 300 kg N/ha. Inclusion of ammonium thiosulfate in the fertiliser formulation did not appear to have a significant impact on fertiliser N recovery.

Soil Research ◽  
2003 ◽  
Vol 41 (2) ◽  
pp. 165 ◽  
Author(s):  
Ram C. Dalal ◽  
Weijin Wang ◽  
G. Philip Robertson ◽  
William J. Parton

Increases in the concentrations of greenhouse gases, carbon dioxide (CO2), methane (CH4), nitrous oxide (N2O), and halocarbons in the atmosphere due to human activities are associated with global climate change. The concentration of N2O has increased by 16% since 1750. Although atmospheric concentration of N2O is much smaller (314 ppb in 1998) than of CO2 (365 ppm), its global warming potential (cumulative radiative forcing) is 296 times that of the latter in a 100-year time horizon. Currently, it contributes about 6% of the overall global warming effect but its contribution from the agricultural sector is about 16%. Of that, almost 80% of N2O is emitted from Australian agricultural lands, originating from N fertilisers (32%), soil disturbance (38%), and animal waste (30%). Nitrous oxide is primarily produced in soil by the activities of microorganisms during nitrification, and denitrification processes. The ratio of N2O to N2 production depends on oxygen supply or water-filled pore space, decomposable organic carbon, N substrate supply, temperature, and pH and salinity. N2O production from soil is sporadic both in time and space, and therefore, it is a challenge to scale up the measurements of N2O emission from a given location and time to regional and national levels.Estimates of N2O emissions from various agricultural systems vary widely. For example, in flooded rice in the Riverina Plains, N2O emissions ranged from 0.02% to 1.4% of fertiliser N applied, whereas in irrigated sugarcane crops, 15.4% of fertiliser was lost over a 4-day period. Nitrous oxide emissions from fertilised dairy pasture soils in Victoria range from 6 to 11 kg N2O-N/ha, whereas in arable cereal cropping, N2O emissions range from <0.01% to 9.9% of N fertiliser applications. Nitrous oxide emissions from soil nitrite and nitrates resulting from residual fertiliser and legumes are rarely studied but probably exceed those from fertilisers, due to frequent wetting and drying cycles over a longer period and larger area. In ley cropping systems, significant N2O losses could occur, from the accumulation of mainly nitrate-N, following mineralisation of organic N from legume-based pastures. Extensive grazed pastures and rangelands contribute annually about 0.2 kg N/ha as N2O (93 kg/ha per year CO2-equivalent). Tropical savannas probably contribute an order of magnitude more, including that from frequent fires. Unfertilised forestry systems may emit less but the fertilised plantations emit more N2O than the extensive grazed pastures. However, currently there are limited data to quantify N2O losses in systems under ley cropping, tropical savannas, and forestry in Australia. Overall, there is a need to examine the emission factors used in estimating national N2O emissions; for example, 1.25% of fertiliser or animal-excreted N appearing as N2O (IPCC 1996). The primary consideration for mitigating N2O emissions from agricultural lands is to match the supply of mineral N (from fertiliser applications, legume-fixed N, organic matter, or manures) to its spatial and temporal needs by crops/pastures/trees. Thus, when appropriate, mineral N supply should be regulated through slow-release (urease and/or nitrification inhibitors, physical coatings, or high C/N ratio materials) or split fertiliser application. Also, N use could be maximised by balancing other nutrient supplies to plants. Moreover, non-legume cover crops could be used to take up residual mineral N following N-fertilised main crops or mineral N accumulated following legume leys. For manure management, the most effective practice is the early application and immediate incorporation of manure into soil to reduce direct N2O emissions as well as secondary emissions from deposition of ammonia volatilised from manure and urine.Current models such as DNDC and DAYCENT can be used to simulate N2O production from soil after parameterisation with the local data, and appropriate modification and verification against the measured N2O emissions under different management practices.In summary, improved estimates of N2O emission from agricultural lands and mitigation options can be achieved by a directed national research program that is of considerable duration, covers sampling season and climate, and combines different techniques (chamber and micrometeorological) using high precision analytical instruments and simulation modelling, under a range of strategic activities in the agriculture sector.


1995 ◽  
Vol 125 (1) ◽  
pp. 25-37 ◽  
Author(s):  
J. Webb ◽  
R. Sylvester-Bradley ◽  
J. D. Wafford

SUMMARYAt 14 sites in the UK, spring wheat (Triticum aestivum) cv. Tonic, was sown on three or four dates at each site between October and March in the 1988/89, 1989/90 and 1990/91 seasons. Responses to spring-applied fertilizer N over the range 0–320 kg/ha were determined. Earlier sowing did not increase uptake of soil N by the crop. Fertilizer N increased grain N offtake by between 25 and 140 kg/ha and yield by between 0·3 and 5·5 t/ha, although grain yield was less responsive to fertilizer N at later sowing dates. Apparent recovery of fertilizer N (AFR) also decreased as sowing was delayed but there was no effect of delayed sowing on the amount of grain produced from each kg of fertilizer N recovered. Because fertilizer N recovery decreased with later sowing, the amount of fertilizer N needed to produce the optimum economic grain yield was not reduced. Neither AFR nor optimum fertilizer (Nopt) was related to optimum yield. Regression of Nopt on the difference between optimum yield and yield without fertilizer N (△y) explained 77% of the variance in Nopt. There was an inverse relationship between △y and soil mineral N (SMN) in spring; regression of △y, on SMN in spring accounted for 29% of the variance in △y Current advisory systems which adjust economic fertilizer N recommendations according to anticipated yield are not justified by these results. Moreover the adjustments made, based on yield expectation, appear about three times as large as those needed to minimize residues of fertilizer N left unrecovered by the crop and to reduce the risk of nitrate leaching in the following winter.


2016 ◽  
Author(s):  
Rongting Xu ◽  
Hanqin Tian ◽  
Chaoqun Lu ◽  
Shufen Pan ◽  
Jian Chen ◽  
...  

Abstract. To accurately assess how increased global nitrous oxide (N2O) emission has affected the climate system requires a robust estimation of the pre-industrial N2O emissions since only the difference between current and pre-industrial emissions represents net drivers of anthropogenic climate change. However, large uncertainty exists in previous estimates of pre-industrial N2O emissions from the land biosphere, while pre-industrial N2O emissions at the finer scales such as regional, biome, or sector have not yet well quantified. In this study, we applied a process-based Dynamic Land Ecosystem Model (DLEM) to estimate the magnitude and spatial patterns of pre-industrial N2O fluxes at the biome-, continental-, and global-level as driven by multiple environmental factors. Uncertainties associated with key parameters were also evaluated. Our study indicates that the mean of the pre-industrial N2O emission was approximately 6.20 Tg N yr−1, with an uncertainty range of 4.76 to 8.13 Tg N yr−1. The estimated N2O emission varied significantly at spatial- and biome-levels. South America, Africa, and Southern Asia accounted for 34.12 %, 23.85 %, 18.93 %, respectively, together contributing of 76.90 % of global total emission. The tropics were identified as the major source of N2O released into the atmosphere, accounting for 64.66 % of the total emission. Our multi-scale estimates with a reasonable uncertainty range provides a robust reference for assessing the climate forcing of anthropogenic N2O emission from the land biosphere.


2017 ◽  
Vol 13 (7) ◽  
pp. 977-990 ◽  
Author(s):  
Rongting Xu ◽  
Hanqin Tian ◽  
Chaoqun Lu ◽  
Shufen Pan ◽  
Jian Chen ◽  
...  

Abstract. To accurately assess how increased global nitrous oxide (N2O) emission has affected the climate system requires a robust estimation of the preindustrial N2O emissions since only the difference between current and preindustrial emissions represents net drivers of anthropogenic climate change. However, large uncertainty exists in previous estimates of preindustrial N2O emissions from the land biosphere, while preindustrial N2O emissions on the finer scales, such as regional, biome, or sector scales, have not been well quantified yet. In this study, we applied a process-based Dynamic Land Ecosystem Model (DLEM) to estimate the magnitude and spatial patterns of preindustrial N2O fluxes at the biome, continental, and global level as driven by multiple environmental factors. Uncertainties associated with key parameters were also evaluated. Our study indicates that the mean of the preindustrial N2O emission was approximately 6.20 Tg N yr−1, with an uncertainty range of 4.76 to 8.13 Tg N yr−1. The estimated N2O emission varied significantly at spatial and biome levels. South America, Africa, and Southern Asia accounted for 34.12, 23.85, and 18.93 %, respectively, together contributing 76.90 % of global total emission. The tropics were identified as the major source of N2O released into the atmosphere, accounting for 64.66 % of the total emission. Our multi-scale estimates provide a robust reference for assessing the climate forcing of anthropogenic N2O emission from the land biosphere


2001 ◽  
Vol 1 ◽  
pp. 320-327
Author(s):  
M.I. Khalil ◽  
A.B. Rosenani ◽  
O. Van Cleemput ◽  
C.I. Fauziah ◽  
J. Shamshuddin

Development of appropriate land management techniques to attain sustainability and increase the N use efficiency of crops in the tropics has been gaining momentum. The nitrous oxides (N2Os) affect global climate change and its contribution from N and C management systems is of great significance. Thus, N transformations and N2O emission during maize-groundnut crop rotation managed with various N sources were studied. Accumulation of nitrate (NO3 –) and its disappearance happened immediately after addition of various N sources, showing liming effect. The mineral N retained for 2–4 weeks depending on the type and amount of N application. The chicken manure showed rapid nitrification in the first week after application during the fallow period, leading to a maximum N2O flux of 9889 μg N2O-N m–2 day– 1. The same plots showed a residual effect by emitting the highest N2O (4053 μg N2O-N m–2 day– 1) during maize cultivation supplied with a halfrate of N fertilizer. Application of N fertilizer only or in combination with crop residues exhibited either lowered fluxes or caused a sink during the groundnut and fallow periods due to small availability of substrates and/or low water-filled pore space (<40%). The annual N2O emission ranged from 1.41 to 3.94 kg N2O-N ha–1; the highest was estimated from the chicken manure plus crop residues and half-rate of inorganic N-amended plots. Results indicates a greater influence of chicken manure on the N transformations and thereby N2O emission.


Atmosphere ◽  
2021 ◽  
Vol 12 (2) ◽  
pp. 223
Author(s):  
John Kormla Nyameasem ◽  
Carsten S. Malisch ◽  
Ralf Loges ◽  
Friedhelm Taube ◽  
Christof Kluß ◽  
...  

Nitrous oxide (N2O) emissions from pastures can vary significantly depending on soil and environmental conditions, nitrogen (N) input, as well as the plant’s ability to take up the N. We tested the hypothesis that legume-based N sources are characterized by significantly lower emission factors than mineral N based dairy systems. Therefore, this study monitored N2O emissions for a minimum of 100 days and up to two growing seasons across a gradient of plant species diversity. Emissions were measured from both grazed pastures and a controlled application of urine and dung using the static chamber method. About 90% of the simulated experiments’ accumulated N2O emissions occurred during the first 60–75 days. The average accumulated N2O emissions were 0.11, 0.87, 0.99, and 0.21 kg ha−1 for control, dung, urine patches, and grazed pastures, respectively. The N uptake efficiency at the excreta patch scale was about 70% for both dung and urine. The highest N2O-N emission factor was less than half compared with the IPCC default (0.3 vs. 0.77), suggesting an overestimation of N2O-N emissions from organically managed pastures in temperate climates. Plant diversity showed no significant effect on N2O emission. However, functional groups were significant (p < 0.05). We concluded that legume-containing pasture systems without a fertilizer addition generally appear capable of utilizing nitrogen inputs from excreta patches efficiently, resulting in low N2O emissions.


Atmosphere ◽  
2020 ◽  
Vol 11 (9) ◽  
pp. 948
Author(s):  
Haeyoung Lee ◽  
Miyoung Ko ◽  
Sumin Kim ◽  
Wonick Seo ◽  
Young-San Park

Nitrous oxide (N2O) is a powerful greenhouse gas and is the largest remaining anthropogenic source of stratospheric ozone-depleting substances as halocarbons return towards preindustrial levels. To verify the N2O emission inventory using inverse analysis, precise and reliable measurements are necessary. In this study, we compared the conventional gas chromatography with the microelectron capture detector method (GC-μECD, Agilent 7890A) with advanced off-axis integrated cavity output spectroscopy (OA-ICOS, Los Gatos, EP-30) for atmospheric N2O measurements at the Jeju Gosan Suwolbong Station (JGS, 126.16° E, 33.30° N, 71.47 m a.s.l) in South Korea. The measurement uncertainties from linearity, repeatability, and reproducibility derived from the two instruments were compared. The values derived from GC-μECD were 2.4 to 8.7 times greater than that of OA-ICOS in all factors at the station. Since these factors affect the measurement quality, the calibration strategy should be well-established to reduce the measurement uncertainty. These uncertainties resulted in biases from the measurement of atmospheric N2O. The parallel inter-comparison experiment was implemented at JGS for 22 months, and the difference in atmospheric N2O was 0.17 ± 0.9 ppb between the two instruments. The significant differences were observed in the nonlinear range of the GC-μECD. Finally, these differences resulted in the over/underestimation of N2O characteristics locally and seasonally. Overall, OA-ICOS has a more robust performance with a lower measurement uncertainty than GC-μECD. Based on this study, we also suggest a calibration strategy for both instruments to achieve precise N2O measurements.


2015 ◽  
Vol 12 (20) ◽  
pp. 5915-5928 ◽  
Author(s):  
Z. Yao ◽  
Y. Wei ◽  
C. Liu ◽  
X. Zheng ◽  
B. Xie

Abstract. Tea plantations are rapidly expanding in China and other countries in the tropical and subtropical zones, but so far there are very few studies including direct measurements of nitrogenous gas fluxes from tea plantations. On the basis of 2-year field measurements from 2012 to 2014, we provided an insight into the assessment of annual nitrous oxide (N2O) and nitric oxide (NO) fluxes from Chinese subtropical tea plantations under three practices of conventional urea application, alternative oilcake incorporation and no nitrogen fertilization. Clearly, the N2O and NO fluxes exhibited large intra- and inter-annual variations, and furthermore, their temporal variability could be well described by a combination of soil environmental factors including soil mineral N, water-filled pore space and temperature, based on a revised "hole-in-the-pipe" model. Averaged over a 2-year study, annual background N2O and NO emissions were approximately 4.0 and 1.6 kg N ha−1 yr−1, respectively. Compared to no nitrogen fertilization, both urea and oilcake application significantly stimulated annual N2O and NO emissions, amounting to 14.4–32.7 kg N2O–N ha−1 yr−1 and at least 12.3–19.4 kg NO–N ha−1 yr−1, respectively. In comparison with conventional urea treatment, on average, the application of organic fertilizer significantly increased N2O emission by 71 % but decreased NO emission by 22 %. Although the magnitude of N2O and NO fluxes was substantially influenced by the source of N, the annual direct emission factors of N fertilizer were estimated to be 2.8–5.9, 2.7–4.0 and 6.8–9.1 % for N2O, NO and N2O+NO, respectively, which are significantly higher than those defaults for global upland croplands. This indicated that the rarely determined N2O and NO formation appeared to be a significant pathway in the nitrogen cycle of tea plantations, which are a potential source of national nitrogenous gases inventory.


2010 ◽  
Vol 34 (5) ◽  
pp. 1653-1665 ◽  
Author(s):  
Josiléia Acordi Zanatta ◽  
Cimélio Bayer ◽  
Frederico C.B. Vieira ◽  
Juliana Gomes ◽  
Michely Tomazi

Nitrogen fertilizers increase the nitrous oxide (N2O) emission and can reduce the methane (CH4) oxidation from agricultural soils. However, the magnitude of this effect is unknown in Southern Brazilian edaphoclimatic conditions, as well as the potential of different sources of mineral N fertilizers in such an effect. The aim of this study was to investigate the effects of different mineral N sources (urea, ammonium sulphate, calcium nitrate, ammonium nitrate, Uran, controlled- release N fertilizer, and urea with urease inhibitor) on N2O and CH4 fluxes from Gleysol in the South of Brazil (Porto Alegre, RS), in comparison to a control treatment without a N application. The experiment was arranged in a randomized block with three replications, and the N fertilizer was applied to corn at the V5 growth stage. Air samples were collected from a static chambers for 15 days after the N application and the N2O and CH4 concentration were determined by gas chromatography. The topmost emissions occurred three days after the N fertilizer application and ranged from 187.8 to 8587.4 µg m-2 h-1 N. The greatest emissions were observed for N-nitric based fertilizers, while N sources with a urease inhibitor and controlled release N presented the smallest values and the N-ammonium and amidic were intermediate. This peak of N2O emissions was related to soil NO3--N (R² = 0.56, p < 0.08) when the soil water-filled pore space was up to 70 % and it indicated that N2O was predominantly produced by a denitrification process in the soil. Soil CH4 fluxes ranged from -30.1 µg m-2 h-1 C (absorption) to +32.5 µg m-2 h-1 C (emission), and the accumulated emission in the period was related to the soil NH4+-N concentration (R² = 0.82, p < 0.001), probably due to enzymatic competition between nitrification and metanotrophy processes. Despite both of the gas fluxes being affected by N fertilizers, in the average of the treatments, the impact on CH4 emission (0.2 kg ha-1 equivalent CO2-C ) was a hundredfold minor than for N2O (132.8 kg ha-1 equivalent CO2-C). Accounting for the N2O and CH4 emissions plus energetic costs of N fertilizers of 1.3 kg CO2-C kg-1 N regarding the manufacture, transport and application, we estimated an environmental impact of N sources ranging from 220.4 to 664.5 kg ha-1 CO2 -C , which can only be partially offset by C sequestration in the soil, as no study in South Brazil reported an annual net soil C accumulation rate larger than 160 kg ha-1 C due to N fertilization. The N2O mitigation can be obtained by the replacement of N-nitric sources by ammonium and amidic fertilizers. Controlled release N fertilizers and urea with urease inhibitor are also potential alternatives to N2O emission mitigation to atmospheric and systematic studies are necessary to quantify their potential in Brazilian agroecosystems.


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