Sample records for n2o flux measurements

  1. N2O eddy covariance fluxes: From field measurements to flux calculation

    NASA Astrophysics Data System (ADS)

    Lognoul, Margaux; Debacq, Alain; Heinesch, Bernard; Aubinet, Marc

    2017-04-01

    From March to October 2016, we performed eddy covariance measurements in a sugar beet crop at the Lonzée Terrestrial Observatory (LTO, candidate ICOS site) in Belgium. N2O and H2O atmospheric concentrations were measured at 10 Hz using a quantum-cascade laser spectrometer (Aerodyne Research, Inc.) and combined to wind speed 3D components measured with a sonic anemometer (Gill HS-50). Flux computation was carried out using the EddyPro Software (LI-COR) with a focus on adaptations needed for tracers like N2O. Data filtering and quality control were performed according to Vickers and Mahrt (1997) and Mauder and Foken (2004). The flags were adapted to N2O time series. In this presentation, different computation steps will be presented. More specifically: 1) Considering that a large proportion of N2O fluxes are small (within ± 0.5 nmol m-2 s-1), the classical stationarity test might lead to excessive data filtering and in such case, some searchers have chosen to use the running mean (RM) as a detrend method over block averaging (BA) and to filter data otherwise. For our dataset, BA mean fluxes combined to the stationarity test did not significantly differ from RM fluxes when the averaging window was 300s or larger, but were significantly larger otherwise, suggesting that significant eddies occurred at the 5-min timescale and that they were not accounted for with a shorter averaging window. 2) The determination of time-lag in the case of N2O fluxes can become tricky for two reasons : (1) the signal amplitude can differ from one time period to the next, making it difficult to use the method of covariance maximization and (2) an additional clock drift can appear if the spectrometer is not logging on the same computer than the anemometer. In our case, the N2O signal was strong enough to solve both problems and to perform time-lag compensation according to the covariance maximization, with a default value equal to the mode of the lag distribution. The automatic time

  2. Tall tower landscape scale N2O flux measurements in a Danish agricultural and urban, coastal area

    NASA Astrophysics Data System (ADS)

    Ibrom, Andreas; Lequy, Émeline; Loubet, Benjamin; Pilegaard, Kim; Ambus, Per

    2015-04-01

    Both technical and natural processes emit the greenhouse gas nitrous oxide (N2O) into the atmosphere. The abundant use of nitrogen (N) as fertiliser increases the concentration of reactive nitrogen (Nr) in the atmosphere, the hydrosphere and in the biosphere, i.e. in terrestrial and aquatic ecosystems. Surplus Nr is distributed across linkages to other spheres until most of it is emitted to the atmosphere as NO, N2O or N2. A complete estimate of the effects from human activities on N2O emissions must therefore include all emissions, the direct emissions and the indirect emissions that happen in interlinked spheres. For this it is necessary to assess the fluxes at least at the landscape scale. The episodic nature and the large spatial variability make it difficult to estimate the direct and indirect emissions in a landscape. Modelling requires not only to include the highly variable microbial processes in the ecosystems that produce N2O but as well the accurate simulation of lateral Nr fluxes and their effects on N2O fluxes in places remote from the primary Nr sources. In this context tall tower N2O flux measurements are particularly useful as they integrate over larger areas and can be run, continuously without disturbing the fluxes. On the other hand these measurements can be difficult to interpret due to difficulties to measure the small concentration fluctuations in the atmosphere at small flux rates and to accurately attribute the measured flux at the tower to the area that generates the flux, i.e. the source area. The Technical University of Denmark (DTU) has established eddy covariance N2O flux measurements on a 125 m tall tower at its Risø Campus as part of the EU research infrastructure project the 'Integrated non-CO2 Greenhouse gas Observing System' (InGOS). The eddy covariance system consisted of a N2O/CO quantum cascade laser, Los Gatos, Mountain View, CA, USA and a 3D sonic anemometer (USA-1), Metek, Elmshorn, Germany. The Risø peninsula lies at the

  3. Combining two complementary micrometeorological methods to measure CH4 and N2O fluxes over pasture

    NASA Astrophysics Data System (ADS)

    Laubach, J.; Barthel, M.; Fraser, A.; Hunt, J. E.; Griffith, D. W. T.

    2015-09-01

    New Zealand's largest industrial sector is pastoral agriculture, giving rise to a large fraction of the country's emissions of methane (CH4) and nitrous oxide (N2O). We designed a system to continuously measure CH4 and N2O fluxes at the field scale on two adjacent pastures that differed with respect to management. At the core of this system was a closed-cell Fourier-transform infrared spectrometer (FTIR), measuring the mole fractions of CH4, N2O and carbon dioxide (CO2) at two heights at each site. In parallel, CO2 fluxes were measured using eddy-covariance instrumentation. We applied two different micrometeorological ratio methods to infer the CH4 and N2O fluxes from their respective mole fractions and the CO2 fluxes. The first is a variant of the flux-gradient method, where it is assumed that the turbulent diffusivities of CH4 and N2O equal that of CO2. This method was reliable when the CO2 mole-fraction difference between heights was at least 4 times greater than the FTIR's resolution of differences. For the second method, the temporal increases of mole fractions in the stable nocturnal boundary layer, which are correlated for concurrently-emitted gases, are used to infer the unknown fluxes of CH4 and N2O from the known flux of CO2. This method was sensitive to "contamination" from trace gas sources other than the pasture of interest and therefore required careful filtering. With both methods combined, estimates of mean daily CH4 and N2O fluxes were obtained for 60 % of days at one site and 77 % at the other. Both methods indicated both sites as net sources of CH4 and N2O. Mean emission rates for one year at the unfertilised, winter-grazed site were 8.2 (± 0.91) nmol CH4 m-2 s-1 and 0.40 (± 0.018) nmol N2O m-2 s-1. During the same year, mean emission rates at the irrigated, fertilised and rotationally-grazed site were 7.0 (± 0.89) nmol CH4 m-2 s-1 and 0.57 (± 0.019) nmol N2O m-2 s-1. At this site, the N2O emissions amounted to 1.19 (± 0.15) % of the

  4. Combining two complementary micrometeorological methods to measure CH4 and N2O fluxes over pasture

    NASA Astrophysics Data System (ADS)

    Laubach, Johannes; Barthel, Matti; Fraser, Anitra; Hunt, John E.; Griffith, David W. T.

    2016-03-01

    New Zealand's largest industrial sector is pastoral agriculture, giving rise to a large fraction of the country's emissions of methane (CH4) and nitrous oxide (N2O). We designed a system to continuously measure CH4 and N2O fluxes at the field scale on two adjacent pastures that differed with respect to management. At the core of this system was a closed-cell Fourier transform infrared (FTIR) spectrometer, which measured the mole fractions of CH4, N2O and carbon dioxide (CO2) at two heights at each site. In parallel, CO2 fluxes were measured using eddy-covariance instrumentation. We applied two different micrometeorological ratio methods to infer the CH4 and N2O fluxes from their respective mole fractions and the CO2 fluxes. The first is a variant of the flux-gradient method, where it is assumed that the turbulent diffusivities of CH4 and N2O equal that of CO2. This method was reliable when the CO2 mole-fraction difference between heights was at least 4 times greater than the FTIR's resolution of differences. For the second method, the temporal increases of mole fractions in the stable nocturnal boundary layer, which are correlated for concurrently emitted gases, are used to infer the unknown fluxes of CH4 and N2O from the known flux of CO2. This method was sensitive to "contamination" from trace gas sources other than the pasture of interest and therefore required careful filtering. With both methods combined, estimates of mean daily CH4 and N2O fluxes were obtained for 56 % of days at one site and 73 % at the other. Both methods indicated both sites as net sources of CH4 and N2O. Mean emission rates for 1 year at the unfertilised, winter-grazed site were 8.9 (±0.79) nmol CH4 m-2 s-1 and 0.38 (±0.018) nmol N2O m-2 s-1. During the same year, mean emission rates at the irrigated, fertilised and rotationally grazed site were 8.9 (±0.79) nmol CH4 m-2 s-1 and 0.58 (±0.020) nmol N2O m-2 s-1. At this site, the N2O emissions amounted to 1.21 (±0.15) % of the nitrogen

  5. A field robot for autonomous laser-based N2O flux measurements

    NASA Astrophysics Data System (ADS)

    Molstad, Lars; Reent Köster, Jan; Bakken, Lars; Dörsch, Peter; Lien, Torgrim; Overskeid, Øyvind; Utstumo, Trygve; Løvås, Daniel; Brevik, Anders

    2014-05-01

    N2O measurements in multi-plot field trials are usually carried out by chamber-based manual gas sampling and subsequent laboratory-based gas chromatographic N2O determination. Spatial and temporal resolution of these measurements are commonly limited by available manpower. However, high spatial and temporal variability of N2O fluxes within individual field plots can add large uncertainties to time- and area-integrated flux estimates. Detailed mapping of this variability would improve these estimates, as well as help our understanding of the factors causing N2O emissions. An autonomous field robot was developed to increase the sampling frequency and to operate outside normal working hours. The base of this system was designed as an open platform able to carry versatile instrumentation. It consists of an electrically motorized platform powered by a lithium-ion battery pack, which is capable of autonomous navigation by means of a combined high precision real-time kinematic (RTK) GPS and an inertial measurement unit (IMU) system. On this platform an elevator is mounted, carrying a lateral boom with a static chamber on each side of the robot. Each chamber is equipped with a frame of plastic foam to seal the chamber when lowered onto the ground by the elevator. N2O flux from the soil covered by the two chambers is sequentially determined by circulating air between each chamber and a laser spectrometer (DLT-100, Los Gatos Research, Mountain View, CA, USA), which monitors the increase in N2O concentration. The target enclosure time is 1 - 2 minutes, but may be longer when emissions are low. CO2 concentrations are determined by a CO2/H2O gas analyzer (LI-840A, LI-COR Inc., Lincoln, NE, USA). Air temperature and air pressure inside both chambers are continuously monitored and logged. Wind speed and direction are monitored by a 3D sonic anemometer on top of the elevator boom. This autonomous field robot can operate during day and night time, and its working hours are only

  6. Coupling of N2O and CO2 fluxes from agriculture in Michigan

    NASA Astrophysics Data System (ADS)

    Cui, M.; Tang, J.; Hastings, M. G.; Gelfand, I.; Tao, L.; Sun, K.

    2012-12-01

    CO2 has been known to cause global warming, and N2O is the largest contributor to the greenhouse gas burden of cropping systems in the United States due to application of fertilizer. In our study, fluxes of N2O and CO2 were measured at two maize fields and one reference grassland from Kellogg Biological Station in Southwest Michigan. Here we compared two measuring systems, traditional GC method and LGR/Li-Cor system. Our initial results show that the two measuring systems are consistent (N2O slope=0.96, R2=0.96; and CO2 slope= 1.03, R2=0.86 measuring from the same chamber). Measurements done in pairs of chambers suggest great spatial variations, despite that the chambers were only 0.5 meter apart. The two systems are still comparable by averaging 8 pairs of chambers distributed within one site. Increase of CO2 fluxes were observed the second day after fertilization, but no significant change of N2O fluxes was shown. After artificial rainfall, boosting N2O fluxes and further increase in CO2 fluxes were demonstrated. Our result indicates that precipitation is necessary before a prominent N2O peak. In our LGR/Li-Cor system, CO was also measured from chambers. Interesting CO fluxes were shown in our experiment. Soil, which is usually considered as a CO sink, emits CO in some chambers during our measurement, which is probably related to the nationwide forest fires and lack of precipitation during the period.

  7. Eddy covariance N2O flux measurements at low flux rates: results from the InGOS campaign in a Danish willow field.

    NASA Astrophysics Data System (ADS)

    Ibrom, Andreas; Brümmer, Christian; Hensen, Arjan; van Asperen, Hella; Carter, Mette S.; Gasche, Rainer; Famulari, Daniela; Kutsch, Werner; Pilegaard, Kim; Ambus, Per

    2014-05-01

    Nitrous oxide (N2O) fluxes from soils are characterised by their high spatial and temporal variability. The fluxes depend on the availability of the substrates for nitrification and denitrification and soil physical and chemical conditions that control the metabolic microbial activity. The sporadic nature of the fluxes and their high sensitivity to alterations of the soil climate put very high demands on measurement approaches. Laser spectroscopy enables accurate and fast response detection of atmospheric N2O concentrations and is used for eddy covariance (EC) flux measurements. Alternatively N2O fluxes can be measured with chambers together with high precision analysers. Differences in the measurement approaches and system designs are expected to have a considerable influence on the accuracy of the flux estimation. This study investigates how three different eddy covariance systems perform in a situation of low N2O fluxes from a flat surface. Chamber flux measurements with differing chamber and analyser designs are used for comparison. In April 2013, the EU research infrastructure project InGOS (http://www.ingos-infrastructure.eu/) organised a campaign of N2O flux measurements in a willow plantation close to the Risø Campus of the Technical University of Denmark. The willow field was harvested in February 2013 and received mineral fertiliser equivalent to 120 kg N ha-1 before the campaign started. Three different eddy covariance systems took part in the campaign: two Aerodyne quantum cascade laser (QCL) based systems and one Los Gatos Research off-axis integrated-cavity-output spectroscopy (ICOS) system for N2O and CO. The sonic anemometers were all installed at 2 m height above the bare ground. Gill R3 type sonic anemometers were used with QCL systems and a Gil HS-50 with the ICOS system. The 10 Hz raw data were analysed with group specific softwares and procedures. The local conditions in the exceptionally cold and dry spring 2013 did not lead to large N2O flux

  8. Evaluation of new flux attribution methods for mapping N2O emissions at the landscape scale from EC measurements

    NASA Astrophysics Data System (ADS)

    Grossel, Agnes; Bureau, Jordan; Loubet, Benjamin; Laville, Patricia; Massad, Raia; Haas, Edwin; Butterbach-Bahl, Klaus; Guimbaud, Christophe; Hénault, Catherine

    2017-04-01

    The objective of this study was to develop and evaluate an attribution method based on a combination of Eddy Covariance (EC) and chamber measurements to map N2O emissions over a 3-km2 area of croplands and forests in France. During 2 months of spring 2015, N2O fluxes were measured (i) by EC at 15 m height and (ii) punctually with a mobile chamber at 16 places within 1-km of EC mast. The attribution method was based on coupling the EC measurements, information on footprints (Loubet et al., 20101) and emission ratios based on crops and fertilizations, calculated based on chamber measurements. The results were evaluated against an independent flux dataset measured by automatic chambers in a wheat field within the area. At the landscape scale, the method estimated a total emission of 114-271 kg N-N2O during the campaign. This new approach allowed estimating continuously N2O emission and better accounting for the spatial variability of N2O emission at the landscape scale.

  9. Regional N2O fluxes in Amazonia derived from aircraft vertical profiles

    NASA Astrophysics Data System (ADS)

    D'Amelio, M. T. S.; Gatti, L. V.; Miller, J. B.; Tans, P.

    2009-11-01

    Nitrous oxide (N2O) is the third most important anthropogenic greenhouse gas. Globally, the main sources of N2O are nitrification and denitrification in soils. About two thirds of the soil emissions occur in the tropics and approximately 20% originate in wet rainforest ecosystems, like the Amazon forest. The work presented here involves aircraft vertical profiles of N2O from the surface to 4 km over two sites in the Eastern and Central Amazon: Tapajós National Forest (SAN) and Cuieiras Biologic Reserve (MAN), and the estimation of N2O fluxes for regions upwind of these sites. To our knowledge, these regional scale N2O measurements in Amazonia are unique and represent a new approach to looking regional scale emissions. The fluxes upwind of MAN exhibited little seasonality, and the annual mean was 2.1±1.0 mg N2O m-2 day-1, higher than that for fluxes upwind of SAN, which averaged 1.5±1.6 mg N2O m-2 day-1. The higher rainfall around the MAN site could explain the higher N2O emissions, as a result of increased soil moisture accelerating microbial nitrification and denitrification processes. For fluxes from the coast to SAN seasonality is present for all years, with high fluxes in the months of March through May, and in November through December. The first peak of N2O flux is strongly associated with the wet season. The second peak of high N2O flux recorded at SAN occurs during the dry season and can not be easily explained. However, about half of the dry season profiles exhibit significant correlations with CO, indicating a larger than expected source of N2O from biomass burning. The average CO:N2O ratio for all profiles sampled during the dry season is 94±77 mol CO:mol N2O and suggests a larger biomass burning contribution to the global N2O budget than previously reported.

  10. Regional N2O fluxes in Amazonia derived from aircraft vertical profiles

    NASA Astrophysics Data System (ADS)

    D'Amelio, M. T. S.; Gatti, L. V.; Miller, J. B.; Tans, P.

    2009-08-01

    Nitrous oxide (N2O) is the third most important anthropogenic greenhouse gas. Globally, the main sources of N2O are nitrification and denitrification in soils. About two thirds of the soil emissions occur in the tropics and approximately 20% originate in wet rainforest ecosystems, like the Amazon forest. The work presented here involves aircraft vertical profiles of N2O from the surface to 4 km over two sites in the Eastern and Central Amazon: Tapajós National Forest (SAN) and Cuieiras Biologic Reserve (MAN), and the estimation of N2O fluxes for regions upwind of these sites. To our knowledge, these regional scale N2O measurements in Amazonia are unique and represent a new approach to looking regional scale emissions. The fluxes upwind of MAN exhibited little seasonality, and the annual mean was 2.1±1.0 mg N2O m-2 day-1, higher than that for fluxes upwind of SAN, which averaged 1.5±1.6 mg N2O m-2 day-1. The higher rainfall around the MAN site could explain the higher N2O emissions. For fluxes from the coast to SAN seasonality is present for all years, with high fluxes in the months of March through May, and in November through December. The first peak of N2O flux is strongly associated with the wet season. The second peak of high N2O flux recorded at SAN occurs during the dry season and can not be easily explained. However, about half of the dry season profiles exhibit significant correlations with CO, indicating a larger than expected source of N2O from biomass burning. The average CO:N2O ratio for all profiles sampled during the dry season is 94±77 mol CO:mol N2O and suggests a larger biomass burning contribution to the global N2O budget than previously reported.

  11. Integrated measurements and modeling of CO2, CH4, and N2O fluxes using soil microsite frequency distributions

    NASA Astrophysics Data System (ADS)

    Davidson, Eric; Sihi, Debjani; Savage, Kathleen

    2017-04-01

    Soil fluxes of greenhouse gases (GHGs) play a significant role as biotic feedbacks to climate change. Production and consumption of carbon dioxide (CO2), methane (CH4), and nitrous oxide (N2O) are affected by complex interactions of temperature, moisture, and substrate supply, which are further complicated by spatial heterogeneity of the soil matrix. Models of belowground processes of these GHGs should be internally consistent with respect to the biophysical processes of gaseous production, consumption, and transport within the soil, including the contrasting effects of oxygen (O2) as either substrate or inhibitor. We installed automated chambers to simultaneously measure soil fluxes of CO2 (using LiCor-IRGA), CH4, and N2O (using Aerodyne quantum cascade laser) along soil moisture gradients at the Howland Forest in Maine, USA. Measured fluxes of these GHGs were used to develop and validate a merged model. While originally intended for aerobic respiration, the core structure of the Dual Arrhenius and Michaelis-Menten (DAMM) model was modified by adding M-M and Arrhenius functions for each GHG production and consumption process, and then using the same diffusion functions for each GHG and for O2. The area under a soil chamber was partitioned according to a log-normal probability distribution function, where only a small fraction of microsites had high available-C. The probability distribution of soil C leads to a simulated distribution of heterotrophic respiration, which translates to a distribution of O2 consumption among microsites. Linking microsite consumption of O2 with a diffusion model generates microsite concentrations of O2, which then determine the distribution of microsite production and consumption of CH4 and N2O, and subsequently their microsite concentrations using the same diffusion function. At many moisture values, there are some microsites of production and some of consumption for each gas, and the resulting simulated microsite concentrations of CH4

  12. Quantifying N2O reduction to N2 based on N2O isotopocules - validation with independent methods (helium incubation and 15N gas flux method)

    NASA Astrophysics Data System (ADS)

    Lewicka-Szczebak, Dominika; Augustin, Jürgen; Giesemann, Anette; Well, Reinhard

    2017-02-01

    Stable isotopic analyses of soil-emitted N2O (δ15Nbulk, δ18O and δ15Nsp = 15N site preference within the linear N2O molecule) may help to quantify N2O reduction to N2, an important but rarely quantified process in the soil nitrogen cycle. The N2O residual fraction (remaining unreduced N2O, rN2O) can be theoretically calculated from the measured isotopic enrichment of the residual N2O. However, various N2O-producing pathways may also influence the N2O isotopic signatures, and hence complicate the application of this isotopic fractionation approach. Here this approach was tested based on laboratory soil incubations with two different soil types, applying two reference methods for quantification of rN2O: helium incubation with direct measurement of N2 flux and the 15N gas flux method. This allowed a comparison of the measured rN2O values with the ones calculated based on isotopic enrichment of residual N2O. The results indicate that the performance of the N2O isotopic fractionation approach is related to the accompanying N2O and N2 source processes and the most critical is the determination of the initial isotopic signature of N2O before reduction (δ0). We show that δ0 can be well determined experimentally if stable in time and then successfully applied for determination of rN2O based on δ15Nsp values. Much more problematic to deal with are temporal changes of δ0 values leading to failure of the approach based on δ15Nsp values only. For this case, we propose here a dual N2O isotopocule mapping approach, where calculations are based on the relation between δ18O and δ15Nsp values. This allows for the simultaneous estimation of the N2O-producing pathways' contribution and the rN2O value.

  13. Background CH4 and N2O fluxes in low-input short rotation coppice

    NASA Astrophysics Data System (ADS)

    Görres, Carolyn-Monika; Zenone, Terenzio; Ceulemans, Reinhart

    2016-04-01

    Extensively managed short rotation coppice systems are characterized by low fluxes of CH4 and N2O. However due to the large global warming potential of these trace gases (GWP100: CH4: 34, N2O: 298), such background fluxes can still significantly contribute to offsetting the CO2 uptake of short rotation coppice systems. Recent technological advances in fast-response CH4 and N2O analysers have improved our capability to capture these background fluxes, but their quantification still remains a challenge. As an example, we present here CH4 and N2O fluxes from a short-rotation bioenergy plantation in Belgium. Poplars have been planted in a double-row system on a loamy sand in 2010 and coppiced in the beginning of 2012 and 2014 (two-year rotation system). In 2013 (June - November) and 2014 (April - August), the plantation's CH4 and N2O fluxes were measured in parallel with an eddy covariance tower (EC) and an automated chamber system (AC). The EC had a detection limit of 13.68 and 0.76 μmol m-2 h-1 for CH4 and N2O, respectively. The median detection limit of the AC was 0.38 and 0.08 μmol m-2 h-1 for CH4 and N2O, respectively. The EC picked up a few high CH4 emission events with daily averages >100 μmol m-2 h-1, but a large proportion of the measured fluxes were within the EC's detection limit. The same was true for the EC-derived N2O fluxes where the daily average flux was often close to the detection limit. Sporadically, some negative (uptake) fluxes of N2O were observed. On the basis of the EC data, no clear link was found between CH4 and N2O fluxes and environmental variables. The problem with fluxes within the EC detection limit is that a significant amount of the values can show the opposite sign, thus "mirroring" the true flux. Subsequently, environmental controls of background trace gas fluxes might be disguised in the analysis. As a next step, it will be tested if potential environmental drivers of background CH4 and N2O fluxes at the plantation can be

  14. Annual dynamics of N2O, CH4 and CO2 fluxes from the agricultural irrigation watersheds in southeast China

    NASA Astrophysics Data System (ADS)

    Wu, S.; Zou, J.; Liu, S.; Chen, J.; Kong, D.; Geng, Y.

    2017-12-01

    Agricultural irrigation watershed covers a large area in southeast of China and is a potentially important source of carbon dioxide (CO2), methane (CH4) and nitrous oxide (N2O). However, the flux magnitudes contribution to the overall catchment greenhouse gas (GHGs) fluxes and their drivers of seasonal variability are limited in agricultural irrigation watersheds. An in-situ observation was performed to measure annual CO2, CH4 and N2O fluxes from an agricultural irrigation watershed in southeast of China from September 2014 to September 2016. GHGs fluxes were measured using floating chambers and a gas exchange model was also used to predict CH4 and N2O fluxes. All GHGs showed varied seasonally with highest fluxes in early summer (July) and lowest in winter. Estimated seasonal CH4-C fluxes (11.5-97.6 mg m-2 hr-1) and N2O-N fluxes (2.8-80.8μg m-2 hr-1) were in relative agreement with measured CH4-C fluxes (0.05-74.9mg m-2 hr-1) and N2O-N fluxes (3.9-68.7μg m-2 hr-1) fluxes using floating chambers. Both CH4 and N2O fluxes were positively related to water temperature. The CH4 fluxes were negatively related to water dissolved oxygen (DO) concentration but positively related to sediment dissolved organic carbon (DOC). The N2O fluxes were positively related to water NH4+ and NO3-. The calculated EF5-r value in this study (mean = 0.0016; range = 0.0013-0.0018) was below the current IPCC (2006) default value of 0.0025. This implied that IPCC methodology may over estimates of N2O emissions associated with nitrogen leaching and runoff from agriculture.

  15. Nitrate loading and CH4 and N2O Flux from headwater streams

    NASA Astrophysics Data System (ADS)

    Sousa, C. H. R. D.; Hilker, T.; Hall, F. G.; Moura, Y. M.; McAdam, E.

    2014-12-01

    Freshwater ecosystems transport and process significant amounts of terrestrial carbon and can be considerable sources of CO2, CH4, and N2O. A great deal of uncertainty, however, remains in both global estimates and our understanding of drivers of freshwater greenhouse gas emissions. Furthermore, small headwater streams have received insufficient attention to date and may contribute disproportionately to global GHG flux. Our objective was to quantify GHG flux and assess the impact of changes in DOC and NO3 concentrations in surface and subsurface water on flux rates in three streams in the Lamprey River watershed in New Hampshire, USA, that contrast in surface water DOC:NO3. We measured DOC, NO3 and dissolved gas concentrations in surface waters of each stream monthly from May 2011 to April 2012. Empirical measurements of reaeration coefficients were used to convert dissolved gas concentrations to fluxes. We found higher GHG concentrations and fluxes in the two streams with high DOC concentrations, particularly gases produced by anaerobic metabolism (CH4, N2O from methanogenesis and denitrification, respectively). The stream with high DOC and high NO3 showed high N2O and low CH4 flux, while the high DOC, low NO3 stream showed high CH4 and low N2O flux. Our results are consistent with a model in which C inputs drive total GHG production, while NO3 input regulates the relative importance of CH4 and N2O by suppressing methanogenesis and stimulating denitrification. The magnitude of GHG fluxes suggests that streams in this region are likely to be small sources of CO2, but potentially important sources of CH4 and N2O. Since CH4 and N2O are many times more powerful than CO2 at trapping heat in the atmosphere, freshwater emissions of these gases have the potential to offset a significant proportion of the climate benefits of the terrestrial carbon sink, a possibility that has not been sufficiently incorporated into climate models.

  16. Nitrate loading and CH4 and N2O Flux from headwater streams

    NASA Astrophysics Data System (ADS)

    Schade, J. D.; Bailio, J.; McDowell, W. H.

    2015-12-01

    Freshwater ecosystems transport and process significant amounts of terrestrial carbon and can be considerable sources of CO2, CH4, and N2O. A great deal of uncertainty, however, remains in both global estimates and our understanding of drivers of freshwater greenhouse gas emissions. Furthermore, small headwater streams have received insufficient attention to date and may contribute disproportionately to global GHG flux. Our objective was to quantify GHG flux and assess the impact of changes in DOC and NO3 concentrations in surface and subsurface water on flux rates in three streams in the Lamprey River watershed in New Hampshire, USA, that contrast in surface water DOC:NO3. We measured DOC, NO3 and dissolved gas concentrations in surface waters of each stream monthly from May 2011 to April 2012. Empirical measurements of reaeration coefficients were used to convert dissolved gas concentrations to fluxes. We found higher GHG concentrations and fluxes in the two streams with high DOC concentrations, particularly gases produced by anaerobic metabolism (CH4, N2O from methanogenesis and denitrification, respectively). The stream with high DOC and high NO3 showed high N2O and low CH4 flux, while the high DOC, low NO3 stream showed high CH4 and low N2O flux. Our results are consistent with a model in which C inputs drive total GHG production, while NO3 input regulates the relative importance of CH4 and N2O by suppressing methanogenesis and stimulating denitrification. The magnitude of GHG fluxes suggests that streams in this region are likely to be small sources of CO2, but potentially important sources of CH4 and N2O. Since CH4 and N2O are many times more powerful than CO2 at trapping heat in the atmosphere, freshwater emissions of these gases have the potential to offset a significant proportion of the climate benefits of the terrestrial carbon sink, a possibility that has not been sufficiently incorporated into climate models.

  17. Gas chromatography vs. quantum cascade laser-based N2O flux measurements using a novel chamber design

    NASA Astrophysics Data System (ADS)

    Brümmer, Christian; Lyshede, Bjarne; Lempio, Dirk; Delorme, Jean-Pierre; Rüffer, Jeremy J.; Fuß, Roland; Moffat, Antje M.; Hurkuck, Miriam; Ibrom, Andreas; Ambus, Per; Flessa, Heinz; Kutsch, Werner L.

    2017-03-01

    , the consistency between GC and QCL-based campaign averages was better under low than under high N2O efflux conditions, although single flux values were highly scattered during the low efflux campaign. Furthermore, the QCL technology provides a useful tool to accurately investigate the highly debated topic of diurnal courses of N2O fluxes and its controlling factors. Our new chamber design protects the measurement spot from unintended shading and minimizes disturbance of throughfall, thereby complying with high quality requirements of long-term observation studies and research infrastructures.

  18. Development of an Open-Path N2O Flux Measurement System for Understanding Agricultural and Soil Emissions

    NASA Astrophysics Data System (ADS)

    Gomez, A.; Silver, J.; Massick, S.; Ochoa, E.; Stanton, A. C.

    2015-12-01

    Nitrous oxide is the third most important greenhouse gas, with an atmospheric lifetime of ~114 years and a global warming impact ~300 times greater than that of CO2. The main cause of nitrous oxide's atmospheric increase is anthropogenic emissions, and over 80% of the current global anthropogenic flux is related to agriculture, including associated land-use change. An accurate assessment of N2O emissions from agriculture is vital not only for understanding the global N2O balance and its impact on climate and also for designing crop systems with lower GHG emissions. This work focuses on the early development of an open path N2O instrument for field deployment, based on quantum cascade laser absorption. With a targeted precision of 0.1 ppb at 10 Hz, this instrument will enable eddy covariance measurements to determine vertical fluxes of N2O. Details of the instrument design, which emphasizes ruggedness and high thermal stability, will be presented along with initial results from outdoor testing of the instrument.

  19. Near-Continuous Isotopic Characterization of Soil N2O Fluxes from Maize Production

    NASA Astrophysics Data System (ADS)

    Anex, R. P.; Francis Clar, J.

    2015-12-01

    Isotopomer ratios of N2O and especially intramolecular 15N site preference (SP) have been proposed as indicators of the sources of N2O and for providing insight into the contributions of different microbial processes. Current knowledge, however, is mainly based on pure culture studies and laboratory flask studies using mass spectrometric analysis. Recent development of laser spectroscopic methods has made possible high-precision, in situ measurements. We present results from a maize production field in Columbia County, Wisconsin, USA. Data were collected from the fertilized maize phase of a maize-soybean rotation. N2O mole fractions and isotopic composition were determined using an automatic gas flux measurement system comprising a set of custom-designed automatic chambers, circulating gas paths and an OA-ICOS N2O Isotope Analyzer (Los Gatos Research, Inc., Model 914-0027). The instrument system allows for up to 15 user programmable soil gas chambers. Wide dynamic range and parts-per-billion precision of OA-ICOS laser absorption instrument allows for extremely rapid estimation of N2O fluxes. Current operational settings provide measurements of N2O and its isotopes every 20 seconds with a precision of 0.1 ± 0.050 PPB. Comparison of measurements from four chambers (two between row and two in-row) show very different aggregate N2O flux, but SP values suggest similar sources from nitrifier denitrification and incomplete bacterial denitrification. SP values reported are being measured throughout the current growing season. To date, the majority of values are consistent with an origin from bacterial denitrification and coincide with periods of high water filled pore space.

  20. N2O fluxes at the soil-atmosphere interface in various ecosystems and the global N2O budget

    NASA Technical Reports Server (NTRS)

    Banin, Amos

    1987-01-01

    The overall purpose of this research task is to study the effects of soil properties and ecosystem variables on N2O exchanges at the soil-atmosphere interface, and to assess their effects on the globle N2O budget. Experimental procedures are implemented in various sites to measure the source/sink relations of N2O at the soil-atmosphere interface over prolonged periods of time as part of the research of biogeochemical cycling in terrestrial ecosystems. A data-base for establishing quantitative correlations between N2O fluxes and soil and environmental parameters that are of potential use for remote sensing, is being developed.

  1. Carbon dioxide(CO2) and nitrous oxide (N2O) fluxes in an agro-ecosystems under changing physical and biological conditions

    NASA Astrophysics Data System (ADS)

    Liang, L.; Eberwein, J.; Oikawa, P.; Jenerette, D.; Grantz, D. A.

    2013-12-01

    Liyin Liang1, Jennifer Eberwein1, Patty Oikawa1, Darrel Jenerette1, David Grantz1 1Department of Botany and Plant Sciences, University of California, Riverside, CA 92521, USA Carbon dioxide (CO2) and nitrous oxide (N2O) are the major greenhouse gases and together produce a strong positive radiative forcing in the atmosphere. The fluxes of CO2 and N2O from soil to atmosphere vary with physical and biological factors, e.g., temperature, soil moisture, pH value, soil organic carbon contents, microorganism communities and so on. Understanding the interactions among these factors is critical to estimation of CO2 and N2O emissions. We investigate these fluxes in an extreme production environment with very high maximum temperatures, at the agricultural experiment station of University of California-Desert Research Center in the Imperial Valley of southern California. In this research, we measured the CO2 and N2O fluxes from soil incubation under controlled laboratory conditions, in surface chambers under field conditions and by eddy covariance. We explore the variation of CO2 and N2O fluxes and relationship between them in this extreme biofuel production environment. The discrete chamber measurements showed that the N2O flux in our field sites is 2.39×0.70 μg N m-2 hr-1, with a 95% confidence interval (CI) from 0.86 to 3.92 μg N m-2 hr-1. Compared to the previous reported value (0.45~26.26 μg N m-2 hr-1) of N2O flux in California, the N2O flux from biofuel crop land is in the lower level, although more observations should be took to confirm it. The N2O flux also shows very high variability within a field of biomass Sorghum, ranging from 0.40 to 8.19 μg N m-2 hr-1 across 11 sites owning to the high variability of physical and biological factors. Soil incubation measurements will be conducted to identify the sources of this variability. The eddy covariance measurements will allow calculation of the CO2 and N2O emissions at the ecosystem level as a step in quantifying

  2. Effect of fertilizer application on NO and N2O fluxes from agricultural fields

    NASA Astrophysics Data System (ADS)

    Harrison, Roy M.; Yamulki, Sirwan; Goulding, K. W. T.; Webster, C. P.

    1995-12-01

    Losses of fertilizer as NO and N2O were studied at Broadbalk field, Rothamsted Experimental Station in England, on which subplots have been subject to differing constant levels of fertilizer application for many years. Fluxes of NO and N2O were measured using open- and closed-chamber techniques, respectively. Fluxes from unfertilized soil ranged from 0.3 to 4.8 ng N m-2 s-1 for NO and 0.23 to 3.0 ng N m-2 s-1 for N2O. The corresponding fluxes from the plot with the highest fertilizer application (92 kg N ha-1 yr-1 as NH4NO3) ranged from 0.5 to 64 ng N m-2 s-1 for NO and 0.4 to 240 ng N m-2 s-1 for N2O. Application of increasing amounts of fertilizer substantially enhanced emission rates of both NO and N2O. However, the amount of increase was controlled by competition between the crop and the microorganisms for the available soil nutrients, and loss of N2O to the atmosphere increased sharply at superoptimal levels of fertilizer application. The fertilizer-derived NO and N2O emissions represented approximately 90% of the total emission of these gases during the 25-day sampling period after fertilizer application. The results suggest that while increasing the amount of fertilizer increases both NO and N2O fluxes simultaneously, the NO/N2O emission ratio decreases. Results from laboratory experiments showed that the magnitude of the fertilizer loss as N2O was strongly affected by the form of the applied fertilizer.

  3. Ground and canopy soil N2O fluxes from smallholder oil palm plantations following deforestation in Sumatra, Indonesia

    NASA Astrophysics Data System (ADS)

    Hassler, Evelyn; Corre, Marife D.; Kurniawan, Syahrul; Allen, Kara; Veldkamp, Edzo

    2017-04-01

    Due to an increasing global demand in cheap oils and biofuels, forest conversion to oil palm plantations is rapidly increasing in Indonesia. Although forest conversion is known to influence soil N2O fluxes, measurements from oil palm are scarce. Our study aimed to (1) quantify changes in soil N2O fluxes with forest conversion to oil palm plantations, (2) quantify the contribution of oil-palm canopy soil (lodged between the stems and leaf axils) to N2O fluxes, and (3) determine their controlling factors. In Jambi, Sumatra, we selected two landscapes that mainly differed in soil texture but both on heavily weathered soils: loam and clay Acrisol soils. Within each landscape, we investigated lowland forest, jungle rubber (rubber trees interspersed in secondary forest), both as the reference (previous) land uses, and the converted oil palm plantations by smallholders. Each land use had four replicate plots within each landscape. Each replicate plot had four permanently placed chambers, and soil N2O fluxes were measured monthly from December 2012 to December 2013 by placing vented static covers on chamber bases for 30 minutes for gas flux measurement. For oil-palm canopy soil, each replicate plot was represented by five oil palms, and each oil palm stem was delineated into three 1-m sections (low, middle, and top) in order to represent possible gradients of canopy soil conditions that influence N2O fluxes. Measurements were conducted from February 2013 to May 2014 by collecting canopy soil from each stem section and incubating it in-situ in an air-tight glass jar. Land-use conversion to smallholder plantations had no effect on soil N-oxide fluxes (P = 0.58 to 0.76) due to the inherently low soil N availability and the low N fertilization rates (commonly 48 to 88 kg N ha-1 yr-1) of smallholder oil palm plantations. Soil N2O fluxes (kg N ha-1 yr-1) were: 0.6 ± 0.1 to 1.2 ± 0.6 from the reference land uses and 1.0 ± 0.2 to 1.1 ± 0.5 from the smallholder oil palm

  4. Edge effects on N2O, NO and CH4 fluxes in two temperate forests.

    PubMed

    Remy, Elyn; Gasche, Rainer; Kiese, Ralf; Wuyts, Karen; Verheyen, Kris; Boeckx, Pascal

    2017-01-01

    Forest ecosystems may act as sinks or sources of nitrogen (N) and carbon (C) compounds, such as the climate relevant trace gases nitrous oxide (N 2 O), nitric oxide (NO) and methane (CH 4 ). Forest edges, which catch more atmospheric deposition, have become important features in European landscapes and elsewhere. Here, we implemented a fully automated measuring system, comprising static and dynamic measuring chambers determining N 2 O, NO and CH 4 fluxes along an edge-to-interior transect in an oak (Q. robur) and a pine (P. nigra) forest in northern Belgium. Each forest was monitored during a 2-week measurement campaign with continuous measurements every 2h. NO emissions were 9-fold higher than N 2 O emissions. The fluxes of NO and CH 4 differed between forest edge and interior, but not for N 2 O. This edge effect was more pronounced in the oak than in the pine forest. In the oak forest, edges emitted less NO (on average 60%) and took up more CH 4 (on average 177%). This suggests that landscape structure can play a role in the atmospheric budgets of these climate relevant trace gases. Soil moisture variation between forest edge and interior was a key variable explaining the magnitude of NO and CH 4 fluxes in our measurement campaign. To better understand the environmental impact of N and C trace gas fluxes from forest edges, additional and long-term measurements in other forest edges are required. Copyright © 2016 Elsevier B.V. All rights reserved.

  5. Temporal integration of soil N2O fluxes: validation of IPNOA station automatic chamber prototype.

    PubMed

    Laville, P; Bosco, S; Volpi, I; Virgili, G; Neri, S; Continanza, D; Bonari, E

    2017-09-04

    The assessment of nitrous oxide (N 2 O) fluxes from agricultural soil surfaces still poses a major challenge to the scientific community. The evaluations of integrated soil fluxes of N 2 O are difficult owing to their lower emissions when compared with CO 2 . These emissions are also sporadic as environmental conditions act as a limiting factor. A station prototype was developed to integrate annual N 2 O and CO 2 emissions using an automatic chamber technique and infrared spectrometers within the LIFE project (IPNOA: LIFE11 ENV/IT/00032). It was installed from June 2014 to October 2015 in an experimental maize field in Tuscany. The detection limits for the fluxes were evaluated up to 1.6 ng N-N 2 O m 2  s -1 and 0.3 μg C-CO 2  m 2  s -1 . A cross-comparison carried out in September 2015 with the "mobile IPNOA prototype"; a high-sensibility transportable instrument already validated provided evidence of very similar values and highlighted flux assessment limitations according to the gas analyzers used. The permanent monitoring device showed that temporal distribution of N 2 O fluxes can be very large and discontinuous over short periods of less than 10 days and that N 2 O fluxes were below the detection limit of the instrumentation during approximately 70% of the measurement time. The N 2 O emission factors were estimated to 1.9% in 2014 and 1.7% in 2015, within the range of IPCC assessments.

  6. Validation of a station-prototype designed to integrate temporally soil N2O fluxes: IPNOA Station prototype.

    NASA Astrophysics Data System (ADS)

    Laville, Patricia; Volpi, Iride; Bosco, Simona; Virgili, Giorgio; Neri, Simone; Continanza, Davide; Bonari, Enrico

    2016-04-01

    Nitrous oxide (N2O) flux measurements from agricultural soil surface still accounts for the scientific community as major challenge. The evaluations of integrated soil N2O fluxes are difficult because these emissions are lower than for the other greenhouse gases sources (CO2, CH4). They are also sporadic, because highly dependent on few environmental conditions acting as limiting factors. Within a LIFE project (IPNOA: LIFE11 ENV/IT/00032) a station prototype was developed to integrate annually N2O and CO2 emissions using automatically chamber technique. Main challenge was to develop a device enough durable to be able of measuring in continuous way CO2 and N2O fluxes with sufficient sensitivity to allow make reliable assessments of soil GHG measurements with minimal technical field interventions. The IPNOA station prototype was developed by West System SRL and was set up during 2 years (2014 -2015) in an experimental maize field in Tuscan. The prototype involved six automatic chambers; the complete measurement cycle was of 2 hours. Each chamber was closing during 20 min and biogas accumulations were monitoring in line with IR spectrometers. Auxiliary's measurements including soil temperatures and water contents as weather data were also monitoring. All data were managed remotely with the same acquisition software installed in the prototype control unit. The operation of the prototype during the two cropping years allowed testing its major features: its ability to evaluate the temporal variation of N2O soil fluxes during a long period with weather conditions and agricultural managements and to prove the interest to have continuous measurements of fluxes. The temporal distribution of N2O fluxes indicated that emissions can be very large and discontinuous over short periods less ten days and that during about 70% of the time N2O fluxes were around detection limit of the instrumentation, evaluated to 2 ng N ha-1 day-1. N2O emission factor assessments were 1.9% in 2014

  7. Organically fertilized tea plantation stimulates N2O emissions and lowers NO fluxes in subtropical China

    NASA Astrophysics Data System (ADS)

    Yao, Z.; Wei, Y.; Liu, C.; Zheng, X.; Xie, B.

    2015-07-01

    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 on nitrogenous gases 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 2 years, 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. 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 N source, the annual direct emission factors of fertilizer N 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.

  8. Organically fertilized tea plantation stimulates N2O emissions and lowers NO fluxes in subtropical China

    NASA Astrophysics Data System (ADS)

    Yao, Z.; Wei, Y.; Liu, C.; Zheng, X.; Xie, B.

    2015-10-01

    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.

  9. Simultaneous retrieval of the solar EUV flux and neutral thermospheric O, O2, N2, and temperature from twilight airglow

    NASA Technical Reports Server (NTRS)

    Fennelly, J. A.; Torr, D. G.; Richards, P. G.; Torr, M. R.

    1994-01-01

    We present a method to retrieve neutral thermospheric composition and the solar EUV flux from ground-based twilight optical measurements of the O(+) ((exp 2)P) 7320 A and O((exp 1)D) 6300 A airglow emissions. The parameters retrieved are the neutral temperature, the O, O2, N2 density profiles, and a scaling factor for the solar EUV flux spectrum. The temperature, solar EUV flux scaling factor, and atomic oxygen density are first retrieved from the 7320-A emission, which are then used with the 6300-A emission to retrieve the O2 and N2 densities. The retrieval techniques have been verified by computer simulations. We have shown that the retrieval technique is able to statistically retrieve values, between 200 and 400 km, within an average error of 3.1 + or - 0.6% for thermospheric temperature, 3.3 + or - 2.0% for atomic oxygen, 2.3 + or - 1.3% for molecular oxygen, and 2.4 + or - 1.3% for molecular nitrogen. The solar EUV flux scaling factor was found to have a retrieval error of 5.1 + or - 2.3%. All the above errors have a confidence level of 95%. The purpose of this paper is to prove the viability and usefulness of the retrieval technique by demonstrating the ability to retrieve known quantities under a realistic simulation of the measurement process, excluding systematic effects.

  10. Using Mid-IR Cavity Ring-Down Spectrometry to Simultaneously Measure N2o, CO2, and CH4 Fluxes: Responses to Ammonium Nitrate Additions in Salt Marshes

    NASA Astrophysics Data System (ADS)

    Brannon, E.; Moseman-Valtierra, S.; Tang, J.; Chen, X.; Martin, R.; Garate, M.

    2014-12-01

    Greenhouse gas emissions from salt marshes, especially of nitrous oxide (N2O), are a central interest because anthropogenic nutrient loads may substantially alter net climatic forcing of these globally significant ecosystems. In a series of lab and field experiments, a new cavity ring down spectrometer (CRDS, Picarro G2508) that uses mid-infrared (mid-IR) frequencies to measure N2O was compared to a near-IR gas analyzer (LGR N2O/CO analyzer). The Picarro G2508 reports N2O as well as CO2 and CH4 concentrations roughly every second at the parts per billion level. Responses of N2O fluxes to experimental ammonium nitrate additions in marsh mesocosms and marsh plots in situ were compared among these analyzers, along with minimum detectable N2O fluxes. At fluxes above 150 μmol N2O m-2 d-1, the Picarro G2508 and LGR analyzers performed similarly in both mesocosm and field plots that had been enriched with ammonium nitrate, however there were significantly lower minimum detectable N2O fluxes (about 1 order of magnitude) for the LGR than for the Picarro. A gas chromatograph (Shimadzu GC 2014) was also used to test calibration of the G2508. These experiments suggest that mid-IR CRDS technology offers a new tool for simultaneous analyses of N2O along with CO2 and CH4, which fills an important need for quantifying the net climatic forcing of ecosystems. However based on relatively high minimum N2O detection levels of the CRDS, it may work best in highly eutrophic environments.

  11. Development of a model to simulate the impact of atmospheric stability on N2O-fluxes from soil

    NASA Astrophysics Data System (ADS)

    Thieme, Christoph; Klein, Christian; Biernath, Christian; Heinlein, Florian; Priesack, Eckart

    2014-05-01

    The trace gas N2O, mainly produced by microorganisms in agricultural soils, is a very stable and thus potent greenhouse gas and is the main contributor for the recent depletion of ozone in the stratosphere. Therefore N2O-emissions need to be mitigated and thus much effort has been made to reveal the causes of N2O-formation in soils. At present some crucial drivers for N2O-fluxes are known, but underlying processes of N2O-fluxes are not yet understood or described adequately. An important shortcoming is the description of the upper boundary layer at the soil-atmosphere interface. Therefore, the aim of this study is to develop a mechanistic simulation model, which considers both the formation of N2O in agricultural soils, and the impact of the atmospheric conditions on the transport of soil-born N2O into the atmosphere. The new model simulates N2O-flux as a function of meteorological values instead of a model that just releases the whole amount of N2O into the atmosphere. For this purpose the modular ecosystem model framework Expert-N, which allows to simulate the formation of N2O in the soils will be extended to a model with a more detailed description of the upper boundary condition at the soil-atmosphere interface. In detail, this is realized in the form of a resistance approach, where N2O-fluxes are constrained by a land-air resistance that depends on a Bulk-Exchange Coefficient, wind speed and a gradient of N2O concentrations in the lower atmosphere. Descriptions of atmospheric stability follow the Monin-Obhukov Similarity Theory. The newly developed model will be validated using Eddy Covariance measurements of N2O-fluxes. Measurement device for the N2O concentrations is a Quantum-Cascade-Dual-Laser produced by Aerodyne Research Inc. (Billerca, Mass., USA). The measurements were conducted on an intensively managed field at the TERENO research farm Scheyern (Germany), which is part of the TERENO Bavarian Alps / Pre-Alps observatory.

  12. Fluxes of CO2, CH4 and N2O at two European beech forests: linking soil gas production profiles with soil and stem fluxes

    NASA Astrophysics Data System (ADS)

    Maier, Martin; Machacova, Katerina; Halaburt, Ellen; Haddad, Sally; Urban, Otmar; Lang, Friederike

    2016-04-01

    Soil and plant surfaces are known to exchange greenhouse gases with the atmosphere. Some gases like nitrous oxide (N2O) and methane (CH4) can be produced and re-consumed in different soil depths and soil compartments, so that elevated concentrations of CH4 or N2O in the soil do not necessarily mean a net efflux from the soil into the atmosphere. Soil aeration, and thus the oxygen status can underlay a large spatial variability within the soil on the plot and profile scale, but also within soil aggregates. Thus, conditions suitable for production and consumption of CH4 and N2O can vary on different scales in the soil. Plant surfaces can also emit or take up CH4 and N2O, and these fluxes can significantly contribute to the net ecosystem exchange. Since roots usually have large intercellular spaces or aerenchyma they may represent preferential transport ways for soil gases, linking possibly elevated soil gas concentrations in the subsoil in a "shortcut" to the atmosphere. We tested the hypothesis that the spatial variability of the soil-atmosphere fluxes of CO2, CH4 and N2O is caused by the heterogeneity in soil properties. Therefore, we measured soil-atmosphere gas fluxes, soil gas concentrations and soil diffusivity profiles and did a small scale field assessment of soil profiles on the measurments plots. We further tried to link vertical profiles of soil gas concentrations and diffusivity to derive the production and consumption profiles, and to link these profiles to the stem-atmosphere flux rates of individual trees. Measurements were conducted in two mountain beech forests with different geographical and climatic conditions (White Carpathians, Czech Republic; Black Forest, Germany). Gas fluxes at stem and soil levels were measured simultaneously using static chamber systems and chromatographic and continuous laser analyses. Monitoring simultaneously vertical soil gas profiles allowed to assess the within-soil gas fluxes, and thus to localize the production and

  13. Annual Greenhouse Gas (CO2, CH4, and N2O) Fluxes Via Ebullition from a Temperate Emergent Wetland

    NASA Astrophysics Data System (ADS)

    Mcnicol, G.; Sturtevant, C. S.; Knox, S. H.; Baldocchi, D. D.; Silver, W. L.

    2014-12-01

    Quantifying wetland greenhouse gas exchange is necessary to evaluate their potential for mitigating climate change via carbon sequestration. However measuring greenhouse gas fluxes of carbon dioxide (CO2), methane (CH4), and nitrous oxide (N2O) in wetlands is difficult due to high spatial and temporal variability, and multiple transport pathways of emission. Transport of biogenic soil gas via highly sporadic ebullition (bubbling) events is often ignored or quantified poorly in wetland greenhouse gas budgets, but can rapidly release large volumes of gas to the atmosphere. To quantify a robust annual ebullition flux we measured rates continuously for a year (2013-2014) using custom-built chambers deployed in a restored emergent wetland located in the Sacramento-San Joaquin Delta, CA. We combined ebullition flux rates with observations of gas concentrations to estimate annual ebullition emissions of CO2, CH4, and N2O and compare flux rates to whole-ecosystem exchange of CO2 and CH4 measured simultaneously by eddy covariance.Mean ebullition flux rates were 18.3 ± 5.6 L m-2 yr-1. Ebullition CH4 concentrations were very high and ranged from 23-76 % with a mean of 47 ± 2.9 %; CO2 concentrations were lower and ranged from 0.7-6.6 % with a mean of 2.8 ± 0.3 %; N2O concentrations were below atmospheric concentrations and ranged from 130-389 ppb(v) with a mean of 257 ± 13 ppb(v). We calculated well-constrained annual ebullition fluxes of: 6.2 ± 1.9 g CH4 m-2 yr-1, 1.0 ± 0.3 g CO2 m-2 yr-1 and 9.3 ± 2.8 mg N2O m-2 yr-1. Methane emissions via ebullition were very large, representing 15-25 % of total wetland CH4 emissions measured at this site, whereas ebullition released only relatively small quantities of CO2 and N2O. Our results demonstrate that large releases of CH4 via ebullition from open water surfaces can be a significant component of restored wetland greenhouse gas budgets.

  14. Direct N2O Fluxes from Agroecosystems in Cold Climates: Importance of Soil Freeze-Thaw

    NASA Astrophysics Data System (ADS)

    Congreves, K. A.; Wagner-Riddle, C.; Abalos, D.; Ambadan, J. T.; Brown, S. E.; Tenuta, M.; Gao, X.; Amiro, B. D.; Berg, A. A.

    2016-12-01

    To develop effective climate change mitigation strategies and reduce N2O emissions, the global contribution of freeze-thaw cycles from croplands must be characterized; we present the first study to do so. Long-term N2O flux datasets from micrometeorological approaches were compiled from two Canadian sites (Elora ON & Glenlea MB). Measurements encompassed a total of 21-yr on 16-ha of land producing annual field crops, yielding an unprecedented record of N2O fluxes (42118 half-hourly values) at sites subjected to freeze-thaw cycles from Nov-Apr. At Elora (the warmer site) N2O flux events were associated with thaw cycles throughout Nov-Apr and the main thaw event took place between mid/end of April when air temperatures rose above 0°C and snow melted. The continental site (Glenlea) did not have significant N2O flux events during the prolonged freeze period, but had considerably higher emissions over the thaw period when soil temperature and liquid water content increased more slowly than Elora. Based on cumulative N2O emissions from both sites (Nov-Apr), emissions were closely related to freezing degree days (FDD). An exponential-to-plateau model significantly fit (p<0.0001, r= 0.72) the relationship between N2O emissions and FDD, characterizing larger N2O emissions as FDD increased (y=1.95 (1-exp-0.00852x), y=cumulative N2O-N kg ha-1 and x=FDD). To estimate the global contribution of N2O emissions from seasonally frozen croplands in the northern hemisphere, we applied the algorithm to a global map of FDD derived from three reanalysis products (ERA-Interim, MERRA-Land, GLDAS-NOAH) combined with MODIS land fraction data for croplands. Average global freeze-thaw induced N2O emissions for croplands was estimated at 1.07 Tg N, though it may range from 0.79 - 1.35 Tg N due to model error and variation. This global contribution of N2O from seasonally frozen cropland soils may be responsible for previously observed discrepancies between top-down and bottom-up approaches.

  15. [Effects of warming and precipitation exclusion on soil N2O fluxes in subtropical forests.

    PubMed

    Tang, Cai di; Zhang, Zheng; Cai, Xiao Zhen; Guo, Jian Fen; Yang, Yu Sheng

    2017-10-01

    In order to explore how soil warming and precipitation exclusion influence soil N2O fluxes, we used related functional genes as markers, and four treatments were set up, i.e. , control (CT), soil warming (W, 5 ℃ above the ambient temperature of the control), 50% precipitation reduction (P), soil warming plus 50% precipitation reduction (WP). The results showed that precipitation exclusion reduced soil ammonium nitrogen concentration significantly. Soil warming decreased soil N2O flux and soil denitrification potential significantly. Soil microbial biomass nitrogen (MBN) in warming treatment (W) and precipitation exclusion treatment (P) was significantly lower than that in the control. The amoA gene abundance of AOA was negatively correlated with MBN and ammonium nitrogen contents, but neither soil nitrification potential nor soil N2O flux was correlated with the amoA gene abundance of AOA. Path analysis showed that the denitrification potential affected soil N2O flux directly, while microbial biomass phosphorus (MBP) and warming affected soil N2O flux indirectly through their direct effects on denitrification potential. Temperature might be the main driver of N2O flux in subtropical forest soils. Global warming would reduce N2O emissions from subtropical forest soils.

  16. N2O fluxes over a corn field from an open-path, laser-based eddy covariance system and static chambers

    NASA Astrophysics Data System (ADS)

    Tao, L.; Pan, D.; Gelfand, I.; Abraha, M.; Moyer, R.; Poe, A.; Sun, K.; Robertson, P.; Zondlo, M. A.

    2015-12-01

    Nitrous oxide (N2O) is important greenhouse and ozone-depleting gase. Although many efforts have been paid to N2O emissions, the spatial and temporal variability of N2O emissions still subject to large uncertainty. Application of the eddy covariance method for N2O emissions research would allow continuous ecosystem level flux measurements. The caveat, however, is need for high precision and high frequency measurements in field. In this study, an open-path, quantum cascade-laser-based eddy covariance N2O sensor has been deployed nearly continuously since May 2015 over a corn field at the W.K. Kellogg Biological Station site in SW Michigan. The field precision of the N2O sensor was assessed to be 0.1 ppbv at 10 Hz, and the total consumption was ~ 40 W, allowing the system to be powered solely by solar panels. The stability of the sensor under different temperature and humidity was tested within an environmental chamber. Spectroscopic experiments and cospectra analyses were carried out to study specific corrections associated with the sensor for eddy covariance techniques, including the line broadening effect due to water vapor and high frequency flux attenuation owning to sample path averaging. Ogive analyses indicated that the high-frequency N2O flux loss due to various damping effects was comparable to those of the CO2 flux. The detection limit of flux was estimated to be 0.3 ng N s-1 m-2 with a flux averaging interval of 30 minutes. The results from the EC system were also compared with ground measurements by standard static chambers (SC). Overall, more than 150 individual chamber measurements were taken within the footprint of the EC system. We found good correlation between the EC and SC methods given the spatiotemporal differences between the two techniques (R2 = 0.75). Both methods detected increased emissions during afternoon as compared to morning and night hours. Differences between EC and SC were also studied by investigating spatial variability with a

  17. Effects of warming on N2O fluxes in a boreal peatland of Permafrost region, Northeast China.

    PubMed

    Cui, Qian; Song, Changchun; Wang, Xianwei; Shi, Fuxi; Yu, Xueyang; Tan, Wenwen

    2018-03-01

    Climate warming is expected to increasingly influence boreal peatlands and alter their greenhouse gases emissions. However, the effects of warming on N 2 O fluxes and the N 2 O budgets were ignored in boreal peatlands. Therefore, in a boreal peatland of permafrost zone in Northeast China, a simulated warming experiment was conducted to investigate the effects of warming on N 2 O fluxes in Betula. Fruticosa community (B. Fruticosa) and Ledum. palustre community (L. palustre) during the growing seasons from 2013 to 2015. Results showed that warming treatment increased air temperature at 1.5m aboveground and soil temperature at 5cm depth by 0.6°C and 2°C, respectively. The average seasonal N 2 O fluxes ranged from 6.62 to 9.34μgm -2 h -1 in the warming plot and ranged from 0.41 to 4.55μgm -2 h -1 in the control plots. Warming treatment increased N 2 O fluxes by 147% and transformed the boreal peatlands from a N 2 O sink to a source. The primary driving factors for N 2 O fluxes were soil temperature and active layer depth, whereas soil moisture showed a weak correlation with N 2 O fluxes. The results indicated that warming promoted N 2 O fluxes by increasing soil temperature and active layer depth in a boreal peatland of permafrost zone in Northeast China. Moreover, elevated N 2 O fluxes persisted in this region will potentially drive a noncarbon feedback to ongoing climate change. Copyright © 2017 Elsevier B.V. All rights reserved.

  18. Impacts of Nitrogen Removal and Re-Application on N2O fluxes from Narragansett Bay: Contrasting Turfgrasses, Salt Marshes, and Wastewater Treatment Systems

    NASA Astrophysics Data System (ADS)

    Brannon, E.; Moseman-Valtierra, S.; Quinn, R. K.; Amador, J.; Brown, R.; Lancellotti, B.; Glennon, K.; Celeste, G.; Craver, V.

    2016-12-01

    Narragansett Bay in Rhode Island is characterized by a substantial, historic bay-wide nitrogen (N) gradient. Centralized wastewater treatment plants (WWTPs) are a major anthropogenic N source. Onsite wastewater treatments systems (OWTS), which serve 1/3 of all households in the state, are another anthropogenic N source. Recent state regulation has prompted upgrades to both WWTPs and OWTS to increase N removal capacities. Although this should lower N loads to Narragansett Bay, it has the potential to increase the flux of nitrous oxide (N2O), a potent greenhouse gas. We measured summer-time (2016) N2O fluxes of a major WWTP (biological N removal system at Field's Point in Providence) and three of the most common advanced OWTS in the Narragansett Bay watershed (Orenco Advantex AX20, BioMicrobics FAST, SeptiTech D Series). We also tested impacts of application of recovered N (biosolids from wastewater sludge) on N2O fluxes from a turfgrass (Schedonerus arundinaceus) and dominant native coastal cordgrass (Spartina alterniflora) in mesocosm experiments. Preliminary results indicate that the largest N2O fluxes (245 ± 72 µmol N2O m-2 h-1) were from the Field's Point WWTP. Significant, but smaller N2O fluxes (6 ± 3 µmol N2O m-2 h-1 were also measured from the OWTS. In contrast, N2O fluxes from the N-enriched native coastal cordgrass and turfgrass mesocosms were often non-detectable. However, fluxes from a few mesocosms (max. of 25 µmol N2O m-2 h-1) were on the same order of magnitude as fluxes from the OWTS. A state-wide budget of N2O emissions from turfgrasses, intertidal marshes, and OWTS will be estimated to determine their significance as sources relative to the Field's Point WWTP. This data will be used to identify areas where N2O fluxes can be minimized in the state of RI.

  19. Continuous Eddy Covariance Measurements of N2O Emissions and Controls from an Intensively Grazed Dairy Farm

    NASA Astrophysics Data System (ADS)

    Schipper, L. A.; Liang, L. L.; Wall, A.; Campbell, D.

    2017-12-01

    New Zealand's greenhouse gas (GHG) inventory is disproportionally dominated by methane and nitrous oxide which account for 54% of emissions. These GHGs are derived from pastoral agriculture that supports dairying and meat production. To date, most studies on quantifying or mitigating agricultural N2O emissions have used flux chamber measurements. Recent advances in detector technology now means that routine field-to-farm scale measurements of N2O emissions might be possible using the eddy covariance technique. In late 2016, we established an eddy covariance tower that measured N2O emissions from a dairy farm under year-round grazing. An Aerodyne quantum cascade laser (QCL) was used to measure N2O, CH4 and H2O concentration at 10 Hz and housed in a weatherproof and insulated enclosure (0.9 m ´ 1.2 m) and powered by mains power (240 VAC). The enclosure maintained a stable setpoint temperature (30±0.2°C) by using underground cooling pipes, fans and recirculating instrument heat. QCL (true 10 Hz digital) and CSAT3B sonic anemometer high frequency data are aligned using Network Time Protocol and EddyPro covariance maximisation during flux processing. Fluxes generally integrated over about 6-8 ha. Stable summertime baseline N2O fluxes (FN2O) were around 12-24 g N2O-N ha-1 d-1 (0.5-1.0 nmol N2O m-2 s-1). Grazing by cows during dry summer resulted in only modest increases in FN2O to 24-48 g N2O-N ha-1 d-1 (1.0-2.0 nmol N2O m-2 s-1). However, the first rain events after grazing resulted in large, short-lived (1-3 days) FN2O pulses reaching peaks of 144-192 g N2O-N ha-1 d-1 (6-8 nmol N2O m-2 s-1). During these elevated N2O emissions, FN2O displayed a significant diurnal signal, with peak fluxes mid-afternoon which was best explained by variation in shallow soil temperature in summer. In winter (both cooler and wetter) FN2O were not as easily explained on a daily basis but were generally greater than summer. Throughout the year, FN2O was strongly dependent on water filled

  20. Temporal dynamics of direct N2O fluxes from agro-ecosystems in cold climates: importance of year-round measurements in multiple cropping systems

    NASA Astrophysics Data System (ADS)

    Wagner-Riddle, C.; Tenuta, M.

    2014-12-01

    Soil N2O fluxes (direct emissions) are highly variable in time and space due to soil, weather and management drivers. In cold climates, freeze/thaw cycles and short growing seasons can enhance soil N2O production contributing to the temporal variability of fluxes. Year-round measurements of N2O fluxes in multiple cropping systems are needed to decrease the uncertainty of annual emission estimates and to devise mitigation practices for emission reduction in cold climates. We have deployed a micrometeorological flux-gradient approach coupled to a tunable diode laser absorption spectroscopy system at two long-term sites in Canada: Elora, Ontario (2000-2014) and Glenlea, Manitoba (2006-2014). Quasi-simultaneous half-hourly flux measurements on four 4-ha fields within a level and aerodynamically homogeneous landscape were obtained allowing for comparison of crop type and/or management practices within and between years. Annual crops such as corn, soybeans, wheat, and barley received typical inorganic fertilizer and/or manure applications, and best management practices such as timing of application and reduced tillage were studied. Perennial grass-alfalfa hayfields were compared to annual crops during selected time periods. Here we synthesize the long-term datasets from these two sites, and quantify the overall contribution of non-growing season (mainly freeze/thaw cycles) and growing season (mainly nitrogen application) to annual emission totals. Uncertainties of regional estimates for cold-climates will be assessed using these long-term datasets.

  1. Do plant species influence soil CO2 and N2O fluxes in a diverse tropical forest?

    Treesearch

    J.L.M. van Haren; R.C. de Oliveira; N. Restrepo-Coupe; L. Hutyra; P. B. de Camargo; Michael Keller; S.R. Saleska

    2010-01-01

    [1] To test whether plant species influence greenhouse gas production in diverse ecosystems, we measured wet season soil CO2 and N2O fluxes close to 300 large (>35 cm in diameter at breast height (DBH)) trees of 15 species at three clay‐rich forest sites in central Amazonia. We found that soil CO2 fluxes were 38% higher near large trees than at control sites >10...

  2. Factors Controlling Fluxes of Nitrous Oxide (N-N2O) in AN Upland Tropical Forest (atlantic Forest) - Brazil, Rio de Janeiro

    NASA Astrophysics Data System (ADS)

    Perry, I.; de Mello, W. Z.; McDowell, W. H.

    2010-12-01

    Atlantic Forest is located along the Brazilian coast and inland to Paraguay and Argentina. It has been largely devastated years ago by anthropogenic activities, such as agriculture and urbanization. Only ten percent of its original area remains (100.000 km2), which is concentrated on high lands. Atlantic Forest is a biodiversity hotspot that receives high nitrogen (N) input through atmospheric deposition in forests of Rio de Janeiro; however, not much is known about the consequences of this N addition. This study has been conducted in the Serra dos Orgaos National Park (SONP - 22.782 km2) located a few kilometers Northeast of Rio de Janeiro Metropolitan Region, Sea Mountain. The forest, characterized as Tropical Moist Forest, is rigorously protected. Vegetation varies along the altitudinal gradient, where the highest peak is at 2,200m asl. Previous studies reported that N atmospheric deposition in SONP varies from 14 to 24 kg ha-1 year-1. The high N deposition on tropical forests increases emission to the atmosphere of N-N2O, a greenhouse gas. There is a lack of N-N2O measurements in tropical forests, mainly in upland tropical forests. We present fluxes of N-N2O from a Brazilian upland tropical forest, and assess the factors controlling N-N2O fluxes. Samples were collected from eight grids (48m2), between 330-451m asl (Subtropical vegetation) and eight grids between 1137-1251m (Montane vegetation), during the dry (July 2008) and wet (Jan-Feb 2009) seasons. Daily, N-N2O (N=372) and soil (N=185) were collected. Nitrous oxide emission was 0,7 (lower altitude) and 0,3 kgN ha-1 year-1 (higher altitude), which is lower than in other upland tropical forests, such as Luquillo Experimental Forest, Puerto Rico, where atmospheric N input (4 kg ha-1 year-1) is not as high as in SONP. Water filled pore space, soil temperature, phosphorus and C:N are the main factors controlling N-N2O fluxes. Manganese was not a good indicator for presence or absence of N-N2O. Higher N-N2O

  3. Effects of the herbicides prosulfuron and metolachlor on fluxes of CO2, N2O, and CH4 in a fertilized Colorado grassland soil

    USGS Publications Warehouse

    Kinney, C.A.; Mosier, A.R.; Ferrer, I.; Furlong, E.T.; Mandernack, K.W.

    2004-01-01

    The effect that pesticides have on trace gas production and consumption in agricultural soils is often overlooked. Independent field and laboratory experiments were used to measure the effects that the commonly used herbicides prosulfuron and metolachlor have on trace gas fluxes (CO2, N2O, and CH4) from fertilized soil of the Colorado shortgrass steppe. Separate sample plots (1 m2) on tilled and no-till soil at the sites included the following treatments: 1) a control without fertilizer or herbicide, 2) a fertilized (NH4NO3 equivalent to 244 kg ha-1) control without herbicide, 3) and fertilized plots amended with an herbicide (prosulfuron equivalent to 0.46 kg ha-1 57% by weight active ingredient or metolachlor equivalent to 5.7 L ha-1, 82.4% by weight active ingredient). During an initial study of one year duration, measurement of gas exchange revealed that prosulfuron-amendment stimulated N2O emissions and CH4 consumption by as much as 1600% and 1300% during a single measurement, respectively. During a second set of flux measurements beginning in August 2001, more frequent weekly measurements were made during a twelve week period. From this second study an increased N2O efflux and CH4 uptake occurred after a 7-week lag period that persisted for about 5 weeks. These changes in gas flux amounted to an overall increase of 41% and 30% for N2O emission and CH4 consumption, respectively. The co-occurrence of stimulated N2O and CH4 fluxes suggests a similar cause that is related to prosulfuron degradation. Evidence suggested that prosulfuron degradation stimulated microbial activity responsible for trace gas flux. Ultimately, prosulfuron-amendment led to an ???50% reduction in the global warming potential from N2O and CH4 fluxes at this field site, which is equivalent to a reduction of the global warming potential of 0.18 mols CO2 m-2 d-1 from these gases. Metolachlor application did not significantly affect the trace gas fluxes measured. These results demonstrate the

  4. Continuous multi-plot measurements of CO2, CH4, N2O and H2O in a managed boreal forest - The importance of accounting for all greenhouse gases

    NASA Astrophysics Data System (ADS)

    Vestin, P.; Mölder, M.; Sundqvist, E.; Båth, A.; Lehner, I.; Weslien, P.; Klemedtsson, L.; Lindroth, A.

    2015-12-01

    In order to assess the effects of different management practices on the exchange of greenhouse gases (GHG), it is desirable to perform repeated and parallel measurements on both experimental and control plots. Here we demonstrate how a system system combining eddy covariance and gradient techniques can be used to perform this assessment in a managed forest ecosystem.The net effects of clear-cutting and stump harvesting on GHG fluxes were studied at the ICOS site Norunda, Sweden. Micrometeorological measurements (i.e., flux-gradient measurements in 3 m tall towers) allowed for quantification of CO2, CH4 and H2O fluxes (from May 2010) as well as N2O and H2O fluxes (from June 2011) at two stump harvested plots and two control plots. There was one wetter and one drier plot of each treatment. Air was continuously sampled at two heights in the towers and gas concentrations were analyzed for CH4, CO2, H2O (LGR DLT-100, Los Gatos Research) and N2O, H2O (QCL Mini Monitor, Aerodyne Research). Friction velocities and sensible heat fluxes were measured by sonic anemometers (Gill Windmaster, Gill Instruments Ltd). Automatic chamber measurements (CO2, CH4, H2O) were carried out in the adjacent forest stand and at the clear-cut during 2010.Average CO2 emissions for the first year ranged between 14.4-20.2 ton CO2 ha-1 yr-1. The clear-cut became waterlogged after harvest and a comparison of flux-gradient data and chamber data (from the adjacent forest stand) indicated a switch from a weak CH4 sink to a significant source at all plots. The CH4 emissions ranged between 0.8-4.5 ton CO2-eq. ha-1 yr-1. N2O emissions ranged between 0.4-2.6 ton CO2-eq. ha-1 yr-1. Enhanced N2O emission on the drier stump harvested plot was the only clear treatment effect on GHG fluxes that was observed. Mean CH4 and N2O emissions for the first year of measurements amounted up to 29% and 20% of the mean annual CO2 emissions, respectively. This highlights the importance of including all GHGs

  5. Effect of N-fertilization on N2 and N2O flux rates in relation to the structure of the denitrifying bacterial community in fen soil

    NASA Astrophysics Data System (ADS)

    Augustin, J.; Behrendt, U.; Ulrich, A.

    2009-04-01

    Drained fen peatlands of north-east Europe managed by different agricultural regimes constitute an important source for emissions of nitrous oxide (N2O) into the atmosphere. The strength of N2O fluxes showed a high variability in time and space influenced by complex interactions of formation and transfer processes with environmental parameters which makes prediction of emissions uncertain. This applies particularly to the denitrification. This is one of the microbial processes with special interest for N2O production in the context of frequently varying soil-moisture content of fen soils that favouring anaerobic conditions. Moreover, denitrification may result in the production of both N2O and N2 in varying proportions. However, not only the knowledge about the effect of soil chemical and physical properties, climate, vegetation, and management on the actual N2O and N2 fluxes is very incomplete at fen soils. There are also no information about the role of structure and activity of denitrifying microbial communities in this context either. The experiments presented in this study aim at addressing this subject matter. Relatively undisturbed soil columns (250 cm3) from a long-term N-fertilization experiment on a fen grassland (over a period of 45 years) were used for measurement of the current N2 and N2O fluxes followed by processing the soil sample for microbiological analysis immediately to investigate the influence of N-fertilization on these parameters. The direct measurement of N2 and N2O fluxes was performed by a helium atmosphere incubation technique in the lab. Results showed a strong influence of N-fertilization and soil moisture on the emission of N2 and N2O. Shifts in the total microbial community were estimated by phospholipid fatty acid analysis, a fingerprint focused on active organisms. Results showed that seasonal effects interfered the influence of N-fertilization on shifts of the total microbial community composition. To characterise the denitrifying

  6. Soil Greenhouse Gas Fluxes, Environmental Controls, and the Partitioning of N2O Sources in UK Natural and Seminatural Land Use Types

    NASA Astrophysics Data System (ADS)

    Sgouridis, Fotis; Ullah, Sami

    2017-10-01

    Natural and seminatural terrestrial ecosystems (unmanaged peatlands and forests and extensive and intensive grasslands) have been under-represented in the UK greenhouse gas (GHG) inventory. Mechanistic studies of GHG fluxes and their controls can improve the prediction of the currently uncertain GHG annual emission estimates. The source apportionment of N2O emissions can further inform management plans for GHG mitigation. We have measured in situ GHG fluxes monthly in two replicated UK catchments and evaluated their environmental controlling factors. An adapted 15N-gas flux method with low addition of 15N tracer (0.03-0.5 kg 15N ha-1) was used to quantify the relative contribution of denitrification to net N2O production. Total N2O fluxes were 40 times higher in the intensive grasslands than in the peatlands (range: -1.32 to 312.3 μg N m-2 h-1). The contribution of denitrification to net N2O emission varied across the land use types and ranged from 9 to 60%. Soil moisture was the key parameter regulating the partitioning of N2O sources (r2 = 0.46). Total N2O fluxes were explained by a simple model (r2 = 0.83) including parameters such as total dissolved nitrogen, organic carbon, and water content. A parsimonious model with the soil moisture content as a single scalar parameter explained 84% of methane flux variability across land uses. The assumption that 1% of the atmospherically deposited N on natural ecosystems is emitted as N2O could be overestimated or underestimated (0.3-1.6%). The use of land use-specific N2O emission factors and further information on N2O source partitioning should help constrain this uncertainty.

  7. The Regulation of CH4 and N2O fluxes by Wetlands at Landscape Level

    NASA Astrophysics Data System (ADS)

    Soosaar, K.; Maddison, M.; Salm, J. O.; Järveoja, J.; Hansen, R.; Mander, Ü.

    2012-04-01

    The world's wetlands, despite being only about 5% of the terrestrial landscape, are currently significant net sinks of more than 1 Pg yr-1 of carbon (Mitsch et al 2012). At landscape level wetlands and riparian zones are important regulators of nutrient transport (Zedler 2003). However, they can be also significant hot spots of greenhouse gas (GHG) emissions (Teiter&Mander 2005). Swedish experience shows that the nationally planned wetland creation (12,000 ha) could make a significant contribution to the targeted reduction of N fluxes (up to 27% of the Swedish environmental objective), at an environmental risk equalling 0.04% of the national anthropogenic GHG emission (Thiere et al 2011). Only few studies consider the potential GHG emission throughout both natural and created wetlands. The main objective of this study was to clarify the potential of various wetland ecosystem and riparian zones of northern rural landscapes in regulation of GHG emissions. Monthly-based measurements of GHG emissions using closed chamber method were performed from October 2007 to October 2011 in 47 study sites in Estonia. The study sites cover various wetlands and riparian forests as well as reference areas on automorphic soils. In general, wetlands' drainage was the most significant disturbance factor influencing GHG fluxes, causing significant increase of N2O emission as well as decreasing CH4 emission. However, we also observed significantly high CH4 flux from drained peatlands. In most of the soils with ground/soil water levels deeper than 30 cm from the surface, a significant decrease of CH4 fluxes were detected. The highest CH4 emissions (up to 5060 kg CH4-C ha-1 yr-1) were detected from drained fen grasslands. In the case of N2O, no clear differences were found between colder and warmer periods. Relatively higher N2O fluxes were measured from the drained fen grassland, the fertilized arable land, the riparian forest on automorphic soil, and the drained transition fen forest

  8. Soil-atmosphere fluxes of the greenhouse gases N2O, CO2 and CH4 from a long term compost experiment in Austria.

    NASA Astrophysics Data System (ADS)

    Spann, Caroline; Spiegel, Heide; Kitzler, Barbara

    2016-04-01

    The application of composts as fertilizers is becoming increasingly important to achieve a closed-loop economy. However, greenhouse gas (GHG) emissions, especially N2O, from agricultural fields may increase as well. In this study different compost types and N amounts were investigated, especially in terms of their GHG fluxes. We used the closed chamber method to estimate GHG flux rates over one vegetation period from an agricultural soil fertilized with different compost types. The study was conducted on a long term compost experiment site near Linz (Austria) with a crop rotation. The soil is a loamy silt and in 2015 maize was planted. Six different compost treatments were investigated. Organic waste compost (OWC) and farmyard manure compost (FMC) was applied with nitrogen concentrations of 175 (OWC1, FYC1) and 525 kg N ha-1 (OWC3, FYC3). Two compost treatments were fertilized additionally with 80 kg N ha.1 mineral fertilizer (OWC2, FYC2). One treatment (TN) was fertilized only with mineral fertilizer (120 kg N ha-1) and one treatment was not fertilized at all (C). Additionally to the GHG flux rates, ammonium and nitrate content, microbial biomass C and N and different enzyme activities were analysed in the top soil. Nitrous oxide (N2O) was emitted over the entire vegetation period with highest fluxes from April until June, until the plants have been established sufficiently. Overall, at the FMC treatments (FYC2, FYC3) highest fluxes were measured. Compared to FMC, lower N2O emissions were measured from the OWC treatments. The combination of compost and mineral N fertilization resulted in the highest N2O emissions, especially after precipitation events. The treatments OWC1 and FYC1 were not different from the control. Methane (CH4) was mainly taken up at all treatments, but uptake rates were lower at the high N input sites (OWC3, FYC3) with no differences between the compost types. No significant differences were found in the soil respiration rates.

  9. Responses of CH(4), CO(2) and N(2)O fluxes to increasing nitrogen deposition in alpine grassland of the Tianshan Mountains.

    PubMed

    Li, Kaihui; Gong, Yanming; Song, Wei; He, Guixiang; Hu, Yukun; Tian, Changyan; Liu, Xuejun

    2012-06-01

    To assess the effects of nitrogen (N) deposition on greenhouse gas (GHG) fluxes in alpine grassland of the Tianshan Mountains in central Asia, CH(4), CO(2) and N(2)O fluxes were measured from June 2010 to May 2011. Nitrogen deposition tended to significantly increase CH(4) uptake, CO(2) and N(2)O emissions at sites receiving N addition compared with those at site without N addition during the growing season, but no significant differences were found for all sites outside the growing season. Air temperature, soil temperature and water content were the important factors that influence CO(2) and N(2)O emissions at year-round scale, indicating that increased temperature and precipitation in the future will exert greater impacts on CO(2) and N(2)O emissions in the alpine grassland. In addition, plant coverage in July was also positively correlated with CO(2) and N(2)O emissions under elevated N deposition rates. The present study will deepen our understanding of N deposition impacts on GHG balance in the alpine grassland ecosystem, and help us assess the global N effects, parameterize Earth System models and inform decision makers. Copyright © 2012 Elsevier Ltd. All rights reserved.

  10. Measuring denitrification after grassland renewal and grassland conversion to cropland by using the 15N gas-flux method

    NASA Astrophysics Data System (ADS)

    Buchen, Caroline; Eschenbach, Wolfram; Flessa, Heinz; Giesemann, Anette; Lewicka-Szczebak, Dominika; Well, Reinhard

    2015-04-01

    Denitrification, the reduction of oxidized forms of inorganic N to N2O and N2 is an important pathway of gaseous nitrogen losses. Measuring denitrification, especially the reduction of N2O to N2, expressed in the product ratio (N2O/(N2O + N2)), is rather difficult and hence rarely performed under field conditions. But using the 15N gas-flux method allows determining N transformation processes in their natural environment. In order to develop effective climate mitigation strategies understanding the N2O source is essential. We used the 15N gas-flux method to determine N2O and N2 emissions following grassland renewal and conversion techniques. Therefore we selected three different treatments: control (C), mechanical grassland renovation (GR) (autumn 2013) and grassland conversion to maize (GM) (spring 2014) from field plot trials on two different sites (Histic Gleysoil and Plaggic Anthrosol) near Oldenburg, Lower Saxony, Germany. We applied 15N labeled KNO3- (60 atom. % 15N) at a rate equivalent to common farming practices (150 kg N*ha-1) using needle injection of fertilizer solution in three different depths (10 cm, 15 cm, 20 cm) for homogeneous soil labeling up to 30 cm in microplots. During the first 10 days after application (May 2014) gas flux measurements from closed chambers were performed every second day and then weekly following a period of 8 weeks. Gas samples were analyzed for δ15N of N2 and N2O by IRMS according to Lewicka-Szczebak et al. (2013). Concentration and 15N enrichment of NO3- in soil water was determined on weekly samples using the SPIN-MAS technique (Stange et al. 2007). Fluxes of N2 and N2O evolved from the 15N labeled soil nitrogen pool were calculated using the equations of Spott et al. (2006). Peak events of N2 and N2O emissions occurred during the first 10 days of measurement, showing differences in soil types, as well as treatment variations. N2 fluxes up to 178 g*ha-1*day-1 and N2O fluxes up to 280 g*ha-1*day-1 were measured on the

  11. A flux-gradient system for simultaneous measurement of the CH4, CO2, and H2O fluxes at a lake-air interface.

    PubMed

    Xiao, Wei; Liu, Shoudong; Li, Hanchao; Xiao, Qitao; Wang, Wei; Hu, Zhenghua; Hu, Cheng; Gao, Yunqiu; Shen, Jing; Zhao, Xiaoyan; Zhang, Mi; Lee, Xuhui

    2014-12-16

    Inland lakes play important roles in water and greenhouse gas cycling in the environment. This study aims to test the performance of a flux-gradient system for simultaneous measurement of the fluxes of water vapor, CO2, and CH4 at a lake-air interface. The concentration gradients over the water surface were measured with an analyzer based on the wavelength-scanned cavity ring-down spectroscopy technology, and the eddy diffusivity was measured with a sonic anemometer. Results of a zero-gradient test indicate a flux measurement precision of 4.8 W m(-2) for water vapor, 0.010 mg m(-2) s(-1) for CO2, and 0.029 μg m(-2) s(-1) for CH4. During the 620 day measurement period, 97%, 69%, and 67% of H2O, CO2, and CH4 hourly fluxes were higher in magnitude than the measurement precision, which confirms that the flux-gradient system had adequate precision for the measurement of the lake-air exchanges. This study illustrates four strengths of the flux-gradient method: (1) the ability to simultaneously measure the flux of H2O, CO2, and CH4; (2) negligibly small density corrections; (3) the ability to resolve small CH4 gradient and flux; and (4) continuous and noninvasive operation. The annual mean CH4 flux (1.8 g CH4 m(-2) year(-1)) at this hypereutrophic lake was close to the median value for inland lakes in the world (1.6 g CH4 m(-2) year(-1)). The system has adequate precision for CH4 flux for broad applications but requires further improvement to resolve small CO2 flux in many lakes.

  12. Interannual Variability in Soil Trace Gas (CO2, N2O, NO) Fluxes and Analysis of Controllers

    NASA Technical Reports Server (NTRS)

    Potter, C.; Klooster, S.; Peterson, David L. (Technical Monitor)

    1997-01-01

    Interannual variability in flux rates of biogenic trace gases must be quantified in order to understand the differences between short-term trends and actual long-term change in biosphere-atmosphere interactions. We simulated interannual patterns (1983-1988) of global trace gas fluxes from soils using the NASA Ames model version of CASA (Carnegie-Ames-Stanford Approach) in a transient simulation mode. This ecosystem model has been recalibrated for simulations driven by satellite vegetation index data from the NOAA Advanced Very High Resolution Radiometer (AVHRR) over the mid-1980s. The predicted interannual pattern of soil heterotropic CO2 emissions indicates that relatively large increases in global carbon flux from soils occurred about three years following the strong El Nino Southern Oscillation (ENSO) event of 1983. Results for the years 1986 and 1987 showed an annual increment of +1 Pg (1015 g) C-CO2 emitted from soils, which tended to dampen the estimated global increase in net ecosystem production with about a two year lag period relative to plant carbon fixation. Zonal discrimination of model results implies that 80-90 percent of the yearly positive increments in soil CO2 emission during 1986-87 were attributable to soil organic matter decomposition in the low-latitudes (between 30 N and 30 S). Soils of the northern middle-latitude zone (between 30 N and 60 N) accounted for the residual of these annual increments. Total annual emissions of nitrogen trace gases (N2O and NO) from soils were estimated to vary from 2-4 percent over the time period modeled, a level of variability which is consistent with predicted interannual fluctuations in global soil CO2 fluxes. Interannual variability of precipitation in tropical and subtropical zones (30 N to 20 S appeared to drive the dynamic inverse relationship between higher annual emissions of NO versus emissions of N2O. Global mean emission rates from natural (heterotrophic) soil sources over the period modeled (1983

  13. Beyond the Methanogenic Black-Box: Greenhouse Gas Fluxes (CO2, CH4, N2O) as Evidence for Wetlands as Dynamic Redox Systems

    NASA Astrophysics Data System (ADS)

    Mcnicol, G.; Knox, S. H.; Sturtevant, C. S.; Baldocchi, D. D.; Silver, W. L.

    2015-12-01

    Seminal wetland research in the 1990s demonstrated that annual methane (CH4) fluxes scaled positively with ecosystem production across distinctive wetlands globally. This relationship implies a model of flooded wetland ecosystems as 'methanogenic black-boxes'; poised at a low redox state, and tending to release a fixed fraction of incoming annual productivity as CH4. In contrast, recent studies have reported high ratios of carbon dioxide (CO2) to CH4 emissions, and are adding to a body of evidence suggesting wetlands can vary more widely in their redox state. To explore this apparent incongruence we used principles of redox thermodynamics and laboratory experiments to develop predictions of wetland greenhouse gas (GHG) fluxes under different redox regimes. We then used a field study to test the hypothesis that ecosystem seasonality in gross primary productivity (GPP) and temperature would drive changes in GHG emissions, mediated by a dynamic - as opposed to static - redox regime. We estimated wetland GHG emissions from an emergent marsh in the Sacramento Delta, CA from March 2014-2015. We measured CO2, CH4 and N2O emissions via diffusion and ebullition with manual sampling, and whole-ecosystem fluxes of CO2 and CH4 using eddy-covariance. Ebullition and diffusive CH4 fluxes were strongly seasonal, with minimum rates (0.86 and 0.35 mg C-CH­­4 m-2 yr-1, respectively) during winter, and maximum rates (1.3 and 1.8 g C-CH­­4 m-2 yr-1, respectively) during the summer growing season. In contrast, winter diffusive CO2 fluxes (494 g C-CO2 m-2 yr-1) and fall bubble CO2 concentrations (1.49%) were highest, despite being seasons of lower GPP, temperature, and CH4 flux. Further, diffusive and ebullition fluxes of N2O showed zero net flux only during spring and summer months, whereas the wetland was a significant source of N2O during winter (81.2 ± 24.4 mg N-N2O m-2 yr-1). These seasonal flux dynamics contradict a 'methanogenic black box' model of wetland redox, which

  14. Sediment-water fluxes of dissolved inorganic carbon, O2,nutrients, and N2 from the hypoxic region of the Louisianacontinental shelf

    EPA Science Inventory

    Sediment fluxes of dissolved inorganic carbon (DIC), O2, nutrients, and N2 (denitrification) were measured on the Louisiana Continental Shelf during six cruises from 2005 to 2007. On each cruise, three to seven stations were occupied in regions of the shelf that experience summer...

  15. Effects of cover crops incorporation and nitrogen fertilization on N2O and CO2 emissions

    NASA Astrophysics Data System (ADS)

    Kandel, T. P.; Gowda, P. H.; Northup, B. K.; DuPont, J.; Somenahally, A. C.; Rocateli, A.

    2017-12-01

    In this study, we measured N2O and CO2 fluxes from plots planted to hairy vetch (winter cover crop) and broadleaf vetch (spring cover crop) as N sources for the following crabgrass (summer forage crop) in El Reno, Oklahoma, USA. Comparisons also included 0 and 60 kg ha-1 mineral N fertilizer supplied as dry urea. No significant N2O fluxes were observed during rapid growing periods of cover crops (March-April, 2017), however, large fluxes were observed after hairy vetch incorporation. Immediately after the hairy vetch biomass incorporation, large rainfall events were recorded. The fluxes subsided gradually with drying soil condition but were enhanced after every consecutive rainfall events. A rainfall induced flux measuring up to 8.2 kg N2O ha-1 day-1 was observed after 26 days of biomass incorporation. In total, 29 kg N2O ha-1 (18 kg N ha-1) was emitted within a month after biomass incorporation from hairy vetch plots. Growth of broadleaf vetch was poor and N2O fluxes were also lower. Similarly, plots fertilized with 60 kg N ha-1 had significant fluxes of N2O but the magnitude was much lower than the hairy vetch plots. Dynamics of N2O and CO fluxes correlated strongly. The results thus indicated that although cover crops may provide many environmental/agronomic benefits such as N fixation, soil carbon built-up, weed suppression and erosion control, high N2O emissions may dwarf these benefits.

  16. Shallow tillage generates higher N2O emissions: results of continuous chamber-based measurement in a winter wheat field.

    NASA Astrophysics Data System (ADS)

    Broux, François; Lognoul, Margaux; Theodorakopoulos, Nicolas; Hiel, Marie-Pierre; Bodson, Bernard; Heinesch, Bernard; Aubinet, Marc

    2017-04-01

    Agriculture is one of the most important contributors to GHG emission, notably through fertilized croplands. Though, few publications have studied simultaneously and through continuous measurement the N2O and CO2 emissions in cultivated lands. We conducted this study to assess the effect of farming practices and climate on both N2O and CO2 emissions from a winter wheat crop. The experiment was held in an experimental field in the loamy region in Belgium from March 2016 till crop harvest in August 2016. The fluxes were measured on two nearby parcels in a winter wheat field with restitution of the residues from previous crop. For the past 8 years, one parcel was subjected to a shallow tillage (ST, 10 cm depth) and the other one to a conventional tillage (CT, 25 cm depth). On each parcel, the emissions are assessed with homemade automated closed chambers. Measurement continuity and good temporal resolution (one mean flux every 4 hours) of the system allowed a fine detection and quantification of the emission peaks which usually represent the major part of N2O fluxes. In addition to gas fluxes, soil water content and temperature were measured continuously. Soil samples were taken regularly to determine soil pH, soil organic carbon and nitrogen pools (total, NO3- and NH4+) and study microbial diversity and nitrification/denitrification gene expression. Unexpectedly, results showed N2O emissions twice as large in the ST parcel as in the CT parcel. On the contrary, less important CO2 emissions were observed under ST. Several emission peaks of N2O were observed during the measurement period. The peaks occurred after fertilization events and seemed to be triggered by an elevation of soil water content. Interesting links could be made between soil NH4-N and NO3-N pools and N2O emissions. Nitrification being the main process originating the fluxes was suggested on the one hand by the temporal evolution of nitrogen pools and N2O emissions and on the other hand by the relation

  17. N2 Fluxes From Amazon Cropland Are a Significant Component of Watershed N Budgets.

    NASA Astrophysics Data System (ADS)

    Fox, R. J.; Neill, C.; Macedo, M.; Davidson, E. A.; Lefebvre, P.; Jankowski, K.; Maracahipes-Santos, L.

    2017-12-01

    Amazon tropical rainforests have experienced significant deforestation and conversion to cropland. Recently, cropping has intensified to include higher application rates of N fertilizer, typically in a soybean-corn rotation. Our previous work in Mato Grosso, Brazil, suggests that the addition of N fertilizer (80 Kg N ha-1 yr-1) has not increased N2O fluxes from soils or elevated dissolved N concentrations in streams or groundwater. Here, we investigate whether N fertilizer is converted to N2 in groundwater. We collected samples during January and October 2016 from streams and well transects across riparian forest buffers bordering cropland or within intact riparian forests. Samples were collected using a positive pressure pump and analyzed using Membrane Inlet Mass Spectrometry (MIMS) for N2, Ar, and O2 and gas chromatography for N2O and CH4. N2 concentrations in excess of solubility (based on Ar) were measured at nearly all locations in January and ranged from -15 to 220 in cropland and -2 to 93 µmol N2-N L-1 in intact forest. N2 concentrations were generally lower in October and ranged from -0.9 to 95 in cropland and -0.6 to 52 µmol N2-N L-1 in intact forest. Higher N2 concentrations accumulated at lower dissolved oxygen concentrations and at the borders between cropland and riparian forest. N2O concentrations were significantly lower than N2 concentrations on both dates and ranged between 0.01 and 0.33 µmol N2O-N L-1. Preliminary estimates suggest that N2 losses from cropland ranged from 10 to 20 kg N ha-1 y-1 and losses from forests ranged from 2 to 12 kg N ha-1 y-1. High concentrations of N2 in groundwater have been found in and around agricultural fields in temperate regions, but direct N2 measurements in tropical agricultural regions have not been previously documented. These results suggest that N2 fluxes from tropical cropland receiving modest amounts of N fertilizer could be substantial.

  18. Oceanic nitrogen cycling and N2O flux perturbations in the Anthropocene

    NASA Astrophysics Data System (ADS)

    Landolfi, A.; Somes, C. J.; Koeve, W.; Zamora, L. M.; Oschlies, A.

    2017-08-01

    There is currently no consensus on how humans are affecting the marine nitrogen (N) cycle, which limits marine biological production and CO2 uptake. Anthropogenic changes in ocean warming, deoxygenation, and atmospheric N deposition can all individually affect the marine N cycle and the oceanic production of the greenhouse gas nitrous oxide (N2O). However, the combined effect of these perturbations on marine N cycling, ocean productivity, and marine N2O production is poorly understood. Here we use an Earth system model of intermediate complexity to investigate the combined effects of estimated 21st century CO2 atmospheric forcing and atmospheric N deposition. Our simulations suggest that anthropogenic perturbations cause only a small imbalance to the N cycle relative to preindustrial conditions (˜+5 Tg N y-1 in 2100). More N loss from water column denitrification in expanded oxygen minimum zones (OMZs) is counteracted by less benthic denitrification, due to the stratification-induced reduction in organic matter export. The larger atmospheric N load is offset by reduced N inputs by marine N2 fixation. Our model predicts a decline in oceanic N2O emissions by 2100. This is induced by the decrease in organic matter export and associated N2O production and by the anthropogenically driven changes in ocean circulation and atmospheric N2O concentrations. After comprehensively accounting for a series of complex physical-biogeochemical interactions, this study suggests that N flux imbalances are limited by biogeochemical feedbacks that help stabilize the marine N inventory against anthropogenic changes. These findings support the hypothesis that strong negative feedbacks regulate the marine N inventory on centennial time scales.

  19. Influences of Root Hydraulic Redistribution on N2O Emissions at AmeriFlux Sites

    NASA Astrophysics Data System (ADS)

    Fu, Congsheng; Lee, Xuhui; Griffis, Timothy J.; Wang, Guiling; Wei, Zhongwang

    2018-05-01

    It has long been suspected that root hydraulic redistribution (HR) affects the carbon and nitrogen cycles. Nitrous oxide (N2O) is an important greenhouse gas and is the primary stratospheric ozone-depleting substance. To our knowledge, the influences of HR on N2O emissions have not been investigated. Here we use the HR schemes of Ryel et al. and Amenu and Kumar incorporated into CLM4.5 to examine N2O emissions at five AmeriFlux sites. The results show that HR reduced N2O emissions by 28-92% in the four natural ecosystems experiencing a dry season, whereas it had a very limited effect on the Corn Belt site that has strong emissions but with no distinct dry season. We hypothesize that N2O emissions in ecosystems with a distinct dry season are likely overestimated by CENTURY-based Earth system models.

  20. Validating soil denitrification models based on laboratory N_{2} and N_{2}O fluxes and underlying processes derived by stable isotope approaches

    NASA Astrophysics Data System (ADS)

    Well, Reinhard; Böttcher, Jürgen; Butterbach-Bahl, Klaus; Dannenmann, Michael; Deppe, Marianna; Dittert, Klaus; Dörsch, Peter; Horn, Marcus; Ippisch, Olaf; Mikutta, Robert; Müller, Carsten; Müller, Christoph; Senbayram, Mehmet; Vogel, Hans-Jörg; Wrage-Mönnig, Nicole

    2016-04-01

    Robust denitrification data suitable to validate soil N2 fluxes in denitrification models are scarce due to methodical limitations and the extreme spatio-temporal heterogeneity of denitrification in soils. Numerical models have become essential tools to predict denitrification at different scales. Model performance could either be tested for total gaseous flux (NO + N2O + N2), individual denitrification products (e.g. N2O and/or NO) or for the effect of denitrification factors (e.g. C-availability, respiration, diffusivity, anaerobic volume, etc.). While there are numerous examples for validating N2O fluxes, there are neither robust field data of N2 fluxes nor sufficiently resolved measurements of control factors used as state variables in the models. To the best of our knowledge there has been only one published validation of modelled soil N2 flux by now, using a laboratory data set to validate an ecosystem model. Hence there is a need for validation data at both, the mesocosm and the field scale including validation of individual denitrification controls. Here we present the concept for collecting model validation data which is be part of the DFG-research unit "Denitrification in Agricultural Soils: Integrated Control and Modelling at Various Scales (DASIM)" starting this year. We will use novel approaches including analysis of stable isotopes, microbial communities, pores structure and organic matter fractions to provide denitrification data sets comprising as much detail on activity and regulation as possible as a basis to validate existing and calibrate new denitrification models that are applied and/or developed by DASIM subprojects. The basic idea is to simulate "field-like" conditions as far as possible in an automated mesocosm system without plants in order to mimic processes in the soil parts not significantly influenced by the rhizosphere (rhizosphere soils are studied by other DASIM projects). Hence, to allow model testing in a wide range of conditions

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

    PubMed

    Merbold, Lutz; Eugster, Werner; Stieger, Jacqueline; Zahniser, Mark; Nelson, David; Buchmann, Nina

    2014-06-01

    The first full greenhouse gas (GHG) flux budget of an intensively managed grassland in Switzerland (Chamau) is presented. The three major trace gases, carbon dioxide (CO2), methane (CH4), and nitrous oxide (N2O) were measured with the eddy covariance (EC) technique. For CO2 concentrations, an open-path infrared gas analyzer was used, while N2O and CH4 concentrations were measured with a recently developed continuous-wave quantum cascade laser absorption spectrometer (QCLAS). We investigated the magnitude of these trace gas emissions after grassland restoration, including ploughing, harrowing, sowing, and fertilization with inorganic and organic fertilizers in 2012. Large peaks of N2O fluxes (20-50 nmol m(-2) s(-1) compared with a <5 nmol m(-2) s(-1) background) were observed during thawing of the soil after the winter period and after mineral fertilizer application followed by re-sowing in the beginning of the summer season. Nitrous oxide (N2O) fluxes were controlled by nitrogen input, plant productivity, soil water content and temperature. Management activities led to increased variations of N2O fluxes up to 14 days after the management event as compared with background fluxes measured during periods without management (<5 nmol m(-2) s(-1)). Fluxes of CO2 remained small until full plant development in early summer 2012. In contrast, methane emissions showed only minor variations over time. The annual GHG flux budget was dominated by N2O (48% contribution) and CO2 emissions (44%). CH4 flux contribution to the annual budget was only minor (8%). We conclude that recently developed multi-species QCLAS in an EC system open new opportunities to determine the temporal variation of N2O and CH4 fluxes, which further allow to quantify annual emissions. With respect to grassland restoration, our study emphasizes the key role of N2O and CO2 losses after ploughing, changing a permanent grassland from a carbon sink to a significant carbon source. © 2014 John Wiley & Sons Ltd.

  2. Measurement of N2O and CH4 soil fluxes from garden, agricultural and natural soils using both closed and open chamber systems coupled with high-precision CRDS analyzer

    NASA Astrophysics Data System (ADS)

    He, Yonggang; Jacobson, Gloria; Alexander, Chris; Fleck, Derek; Hoffnagel, John; Del Campo, Bernardo; Rella, Chris

    2013-04-01

    Studying the emission and uptake of greenhouse gases from soil is essential for understanding, adapting to and ultimately mitigating the effects of climate change. To-date, majority of such studies have been focused on carbon dioxide (CO2 ) , however, in 2006 the EPA estimated that "Agricultural activities currently generate the largest share, 63 percent, of the world's anthropogenic non-carbon dioxide (non-CO2) emissions (84 percent of nitrous oxide [N2O] and 52 percent of methane[CH4]), and make up roughly 15 percent of all anthropogenic greenhouse gas emissions" (Prentice et al., 2001). Therefore, enabling accurate N2O and CH4 flux measurements in the field are clearly critical to our ability to better constrain carbon and nitrogen budgets, characterize soil sensitivities, agricultural practices, and microbial processes like denitrification and nitrification. To aide in these studies, Picarro has developed a new analyzer based on its proven, NIR technology platform, which is capable of measuring both N2O and CH4 down to ppb levels in a single, field-deployable analyzer. This analyzer measures N2O with a 1-sigma, precision of 3.5 ppb and CH4 with a 1-sigma precision of 3ppb on a 5 minute average. The instrument also has extremely low drift to enable accurate measurements with infrequent calibrations. The data rate of the analyzer is on the order of 5 seconds in order to capture fast, episodic emission events. One of the keys to making accurate CRDS measurements is to thoroughly characterize and correct for spectral interfering species. This is especially important for closed system soil chambers used on agricultural soils where a variety of soil amendments may be applied and gases not usually present in ambient air could concentrate to high levels. In this work, we present the results of analyzer interference testing and corrections completed for the interference of carbon dioxide, methane, ammonia, ethane, ethylene, acetylene, and water on N2O. In addition, we

  3. Growing season CH4 and N2O fluxes from a subarctic landscape in northern Finland; from chamber to landscape scale

    NASA Astrophysics Data System (ADS)

    Dinsmore, Kerry J.; Drewer, Julia; Levy, Peter E.; George, Charles; Lohila, Annalea; Aurela, Mika; Skiba, Ute M.

    2017-02-01

    Subarctic and boreal emissions of CH4 are important contributors to the atmospheric greenhouse gas (GHG) balance and subsequently the global radiative forcing. Whilst N2O emissions may be lower, the much greater radiative forcing they produce justifies their inclusion in GHG studies. In addition to the quantification of flux magnitude, it is essential that we understand the drivers of emissions to be able to accurately predict climate-driven changes and potential feedback mechanisms. Hence this study aims to increase our understanding of what drives fluxes of CH4 and N2O in a subarctic forest/wetland landscape during peak summer conditions and into the shoulder season, exploring both spatial and temporal variability, and uses satellite-derived spectral data to extrapolate from chamber-scale fluxes to a 2 km × 2 km landscape area.From static chamber measurements made during summer and autumn campaigns in 2012 in the Sodankylä region of northern Finland, we concluded that wetlands represent a significant source of CH4 (3.35 ± 0.44 mg C m-2 h-1 during the summer campaign and 0.62 ± 0.09 mg C m-2 h-1 during the autumn campaign), whilst the surrounding forests represent a small sink (-0.06 ± < 0.01 mg C m-2 h-1 during the summer campaign and -0.03 ± < 0.01 mg C m-2 h-1 during the autumn campaign). N2O fluxes were near-zero across both ecosystems.We found a weak negative relationship between CH4 emissions and water table depth in the wetland, with emissions decreasing as the water table approached and flooded the soil surface and a positive relationship between CH4 emissions and the presence of Sphagnum mosses. Temperature was also an important driver of CH4 with emissions increasing to a peak at approximately 12 °C. Little could be determined about the drivers of N2O emissions given the small magnitude of the fluxes.A multiple regression modelling approach was used to describe CH4 emissions based on spectral data from PLEIADES PA1 satellite imagery across a 2 km

  4. Continuous measurements of N2O emissions from arable fields

    NASA Astrophysics Data System (ADS)

    Wallman, Magdalena; Lammirato, Carlo; Rütting, Tobias; Delin, Sofia; Weslien, Per; Klemedtsson, Leif

    2017-04-01

    al. (eds.)]. Cambridge University Press, Cambridge, United Kingdom and New York, USA. Flessa, H., R. Ruser, R. Schilling, N. Loftfield, J.C. Munch, E.A. Kaiser and F. Beese, 2002. N2O and CH4 fluxes in potato fields: automated measurement, management effects and temporal variation. Geoderma 105(3-4): 307-325. Hénault, C., A. Grossel, B. Mary, M. Roussel and J. Léonard, 2012. Nitrous Oxide Emission by Agricultural Soils: A Review of Spatial and Temporal Variability for Mitigation. Pedosphere 22(4): 426-433. Senapati, N., A. Chabbi, A. Faé Giostri, J. B. Yeluripati and P. Smith, 2016. Modelling nitrous oxide emissions frommown-grass and grain-cropping systems: Testing and sensitivity analysis of DailyDayCent using high frequency measurements. Science of the Total Environment 572: 955-977.

  5. Wetlands and Agriculture in Africa: Major Sources of N2O?

    NASA Astrophysics Data System (ADS)

    Gettel, G. M.

    2015-12-01

    Papyrus wetlands in East Africa are rapidly being converted to agricultural production in an effort to increase food security. This conversion is often seasonal, with wetlands being used for grazing and crop production of maize, sugarcane, and rice during dry seasons, and flooding occurring during wet seasons. An important question with respect to greenhouse gas production is whether wetland conversion to agriculture increases N2O fluxes. This trend has been shown in temperate regions where increased N2O fluxes are positively related to low soil C:N ratios, especially when soil moisture content remains high. In order to examine whether denitrification contributes to N2O flux, we measured potential denitrification rates (PDR by acetylene block method) in intact papyrus wetlands and agricultural converted wetlands in Kenya, Tanzania, Uganda, and Rwanda, and also performed multivariate analysis to relate soil characteristics to PDR. Agricultural land-cover types included maize, sugarcane, rice, and grazing. Results showed that intact wetlands are potentially important sources of N2O, as PDR in papyrus vegetation were consistently the highest (p<0.05; 128 - 601 μg N2O g DW-1 hour-1) while grazing sites showed the lowest (0.1 - 0.5 μg N2O g DW-1 hour-1). Rates were second highest in rice fields (2.3 - 303 μg N2O g DW-1 hour-1), and intermediate in maize and sugarcane (6.5 - 75 μmg N2O g DW-1 hour-1 and 5 - 30 μg N2O g DW-1 hour-1 respectively). PDR across all sites was inversely related to soil C:N ratio, with nitrate consistently limiting PDR in the wetland sites while soil carbon limited PDR in agricultural sites. This is seemingly in contrast with other findings that show that lower C:N ratios result in high N2O fluxes from drained wetland sites. However, flux measurements along with more realistic process-based measurements of denitrification are urgently needed to more fully understand the effect of agricultural conversion of wetlands in East Africa.

  6. Fluxes of N2O and CH4 from forest and grassland lysimeter soils in response to simulated climate change

    NASA Astrophysics Data System (ADS)

    Weymann, Daniel; Brueggemann, Nicolas; Puetz, Thomas; Vereecken, Harry

    2015-04-01

    Central Europe is expected to be exposed to altered temperature and hydrological conditions, which will affect the vulnerability of nitrogen and carbon cycling in soils and thus production and fluxes of climate relevant trace gases. However, knowledge of the response of greenhouse gas fluxes to climate change is limited so far, but will be an important basis for future climate projections. Here we present preliminary results of an ongoing lysimeter field study which aims to assess the impact of simulated climate change on N2O and CH4 fluxes from a forest and a fertilized grassland soil. The lysimeters are part of the Germany-wide research infrastructure TERENO, which investigates feedbacks of climate change to the pedosphere on a long-term scale. Lysimeters (A = 1m2) were established in 2010 at high elevated sites (HE, 500 and 600 m.a.s.l.) and subsequently transferred along an altitudinal gradient to a low elevated site (LE, 100 m.a.s.l.) within the Eifel / Lower Rhine Valley Observatory in Western Germany, thereby resulting in a temperature increase of 2.3 K whereas precipitation decreased by 160 mm during the present study period. Systematic monitoring of soil-atmosphere exchange of N2O and CH4 based on weekly manual closed chamber measurements at HE and LE sites has started in August 2013. Furthermore, we routinely determine dissolved N2O and CH4 concentrations in the seepage water using a headspace equilibration technique and record water discharge in order to quantify leaching losses of both greenhouse gases. Cumulative N2O fluxes clearly responded to simulated climate change conditions and increased by 250 % and 600 % for the forest and the grassland soil, respectively. This difference between the HE and LE sites was mainly caused by an exceptionally heavy precipitation event in July 2014 which turned the LE site sustainably to a consistently higher emission level. Nonetheless, emissions remained rather small and ranged between 20 and 40 μg m-2 h-1. In

  7. SOIL FLUXES OF CO2, CO, NO AND N2O FROM AN OLD-PASTURE AND FROM NATIVE SAVANNA IN BRAZIL

    EPA Science Inventory

    We compared fluxes of CO2, CO, NO and N2O, soil microbial biomass, and N-mineralization rates in a 20-year old Brachiaria pasture and a native cerrado area (savanna in Central Brazil). In order to assess the spatial variability of CO2 fluxes, we tested the relation between elect...

  8. Linking Annual N2O Emission in Organic Soils to Mineral Nitrogen Input as Estimated by Heterotrophic Respiration and Soil C/N Ratio

    PubMed Central

    Mu, Zhijian; Huang, Aiying; Ni, Jiupai; Xie, Deti

    2014-01-01

    Organic soils are an important source of N2O, but global estimates of these fluxes remain uncertain because measurements are sparse. We tested the hypothesis that N2O fluxes can be predicted from estimates of mineral nitrogen input, calculated from readily-available measurements of CO2 flux and soil C/N ratio. From studies of organic soils throughout the world, we compiled a data set of annual CO2 and N2O fluxes which were measured concurrently. The input of soil mineral nitrogen in these studies was estimated from applied fertilizer nitrogen and organic nitrogen mineralization. The latter was calculated by dividing the rate of soil heterotrophic respiration by soil C/N ratio. This index of mineral nitrogen input explained up to 69% of the overall variability of N2O fluxes, whereas CO2 flux or soil C/N ratio alone explained only 49% and 36% of the variability, respectively. Including water table level in the model, along with mineral nitrogen input, further improved the model with the explanatory proportion of variability in N2O flux increasing to 75%. Unlike grassland or cropland soils, forest soils were evidently nitrogen-limited, so water table level had no significant effect on N2O flux. Our proposed approach, which uses the product of soil-derived CO2 flux and the inverse of soil C/N ratio as a proxy for nitrogen mineralization, shows promise for estimating regional or global N2O fluxes from organic soils, although some further enhancements may be warranted. PMID:24798347

  9. Linking annual N2O emission in organic soils to mineral nitrogen input as estimated by heterotrophic respiration and soil C/N ratio.

    PubMed

    Mu, Zhijian; Huang, Aiying; Ni, Jiupai; Xie, Deti

    2014-01-01

    Organic soils are an important source of N2O, but global estimates of these fluxes remain uncertain because measurements are sparse. We tested the hypothesis that N2O fluxes can be predicted from estimates of mineral nitrogen input, calculated from readily-available measurements of CO2 flux and soil C/N ratio. From studies of organic soils throughout the world, we compiled a data set of annual CO2 and N2O fluxes which were measured concurrently. The input of soil mineral nitrogen in these studies was estimated from applied fertilizer nitrogen and organic nitrogen mineralization. The latter was calculated by dividing the rate of soil heterotrophic respiration by soil C/N ratio. This index of mineral nitrogen input explained up to 69% of the overall variability of N2O fluxes, whereas CO2 flux or soil C/N ratio alone explained only 49% and 36% of the variability, respectively. Including water table level in the model, along with mineral nitrogen input, further improved the model with the explanatory proportion of variability in N2O flux increasing to 75%. Unlike grassland or cropland soils, forest soils were evidently nitrogen-limited, so water table level had no significant effect on N2O flux. Our proposed approach, which uses the product of soil-derived CO2 flux and the inverse of soil C/N ratio as a proxy for nitrogen mineralization, shows promise for estimating regional or global N2O fluxes from organic soils, although some further enhancements may be warranted.

  10. Affect of dairy cow manure, urine, and slurry on N<2>O, CO<2>, and CH<4> emissions from Pasture

    NASA Astrophysics Data System (ADS)

    Dorich, C.; Varner, R. K.; Contosta, A.; Li, C.

    2012-12-01

    Agriculture is responsible for roughly 25% of total anthropogenic emission of greenhouse gases (GHG) globally. These agricultural emissions are primarily in the form of methane (CH<4>) and nitrous oxide (N<2>O) where they account for roughly 40 and 80 percent of anthropogenic emissions of their gas, respectively. Measuring and modeling of these gases has remained difficult however as management varies between farms and N<2>O fluxes have been difficult to link to climate and site conditions. Most of these N<2>O fluxes occur during soil freeze-thaw and wetting-drying cycles as well as fertilizer addition moments, all of which are difficult to measure and harder yet to model. Thus the N<2>O flux remains poorly understood and may be underestimated in literature. This provides a problem in agriculture emissions as N use efficiency has been suggested as a proxy for farm scale emissions. On a farm scale these large fluxes of N<2>O from soil "hot moments" can account for up to 60% of the total GHG emissions and thus it is essential to capture the full flux. At the University of New Hampshire Agriculture Experiment Station's (NHAES) organic dairy farm a manure fertilizer experiment was conducted. Manure, urine, and slurry from the UNH dairy farms were collected, analyzed, and applied to pasture plots in May 2012 in order to examine N<2>O flux hot moments. Sites were measured at least bi-weekly with manual static flux chambers taken with soil temperature and moisture along with measurements for soil inorganic N, soil C:N, plant biomass and C:N, and soil pH. Gas samples were analyzed for CO<2>, CH<4>, and N<2>O. Emissions were compared with other fluxes from the farm ecosystem including; corn silage, free stall bedding, composting and solid manure, and a manure slurry tank.

  11. Estimation of nocturnal CO2 and N2O soil emissions from changes in surface boundary layer mass storage

    NASA Astrophysics Data System (ADS)

    Grant, Richard H.; Omonode, Rex A.

    2018-04-01

    Annual budgets of greenhouse and other trace gases require knowledge of the emissions throughout the year. Unfortunately, emissions into the surface boundary layer during stable, calm nocturnal periods are not measurable using most micrometeorological methods due to non-stationarity and uncoupled flow. However, during nocturnal periods with very light winds, carbon dioxide (CO2) and nitrous oxide (N2O) frequently accumulate near the surface and this mass accumulation can be used to determine emissions. Gas concentrations were measured at four heights (one within and three above canopy) and turbulence was measured at three heights above a mature 2.5 m maize canopy from 23 July to 10 September 2015. Nocturnal CO2 and N2O fluxes from the canopy were determined using the accumulation of mass within a 6.3 m control volume and out the top of the control volume within the nocturnal surface boundary layer. Diffusive fluxes were estimated by flux gradient method. The total accumulative and diffusive fluxes during near-calm nights (friction velocities < 0.05 ms-1) averaged 1.16 µmol m-2 s-1 CO2 and 0.53 nmol m-2 s-1 N2O. Fluxes were also measured using chambers. Daily mean CO2 fluxes determined by the accumulation method were 90 to 130 % of those determined using soil chambers. Daily mean N2O fluxes determined by the accumulation method were 60 to 80 % of that determined using soil chambers. The better signal-to-noise ratios of the chamber method for CO2 over N2O, non-stationary flow, assumed Schmidt numbers, and anemometer tilt were likely contributing reasons for the differences in chambers versus accumulated nocturnal mass flux estimates. Near-surface N2O accumulative flux measurements in more homogeneous regions and with greater depth are needed to confirm the conclusion that mass accumulation can be effectively used to estimate soil emissions during nearly calm nights.

  12. No Memory Effects of Restoration on N2O Exchange above an intensively managed Grassland in Switzerland

    NASA Astrophysics Data System (ADS)

    Merbold, L.; Decock, C.; Hörtnagl, L. J.; Fuchs, K.; Eugster, W.

    2015-12-01

    Here we present 3 consecutive years of EC flux measurements of N2O, CH4 and CO2) carried out in intensively managed grassland in Switzerland. Our measurements of greenhouse gas (GHG) concentrations were based on a recently developed CW-QCL absorption spectrometer to measure the concentrations of N2O and CH4 and an infrared gas analyzer to measure the concentrations of CO2 and H2O. We investigated the magnitude of trace gas emissions during a year of major disturbance (grassland restoration - including ploughing and fertilization in 2012) and the two following years representing business as usual (up to 6 harvests per year which are followed by fertilizer application, 2013 and 2014). We observed large peaks of N2O (up to 50 nmol m-2 s-1) in 2012 during thawing of the soil after the winter period and after re-sowing as well as inorganic fertilizer application at the beginning of summer. N2O emissions following harvest and fertilizer application ranged between 2 and 7 nmol m-2 s-1 and background fluxes were no larger than 1 nmol m-2 s-1. Fluxes of N2O were primarily controlled by soil water content and temperature, while management activities lead to larger variation of N2O fluxes during several days after the management event when compared to the background flux measurements. Annual flux budgets were dominated by CO2 emissions and N2O emissions contributed largely to the annual budget in 2012 but to a much lesser extend in the post-disturbance years (2013/2014). CH4 flux contribution to the annual budget was negligible. We conclude that grassland restoration results in large N2O emissions, while not leading to larger N2O emissions in subsequent years. Still, such specific time periods of enhanced N2O emissions need to be considered in decadal greenhouse gas budget estimates due to the fact that a single year can offset previous carbon and nitrogen sinks.

  13. Effects of Eriophorum vaginatum on N_{2}O emissions at a restored peatland

    NASA Astrophysics Data System (ADS)

    Brummell, Martin; Lazcano, Cristina; Strack, Maria

    2016-04-01

    Restoration of peatlands extracted for horticultural peat production includes both deliberate and accidental introduction of a wide range of plant species, including vascular plants and bryophytes. The roots of vascular plants provide a channel for the movement of greenhouse gases (GHG) including N2O in many soil ecosystems, and may stimulate production of N2O or have other effects via the release of root exudates that are then taken up by soil microorganisms such as heterotrophic denitrifiers. Here we carried out a field study in order to evaluate the effects of Eriophorum vaginatum, an abundant sedge at the harvested peatland at Seba Beach, Alberta, Canada, (53° 27'17.2"N 114° 52'52.0"W) where restoration efforts began in late 2012, and is the dominant ground cover in some areas. We hypothesized that E. vaginatum would increase net N2O production from peat compared to areas of bare peat or moss. We measured net GHG exchange for CO2, CH4, and N2O over one growing season (May-September 2015) using static chambers within this peatland to compare between plots containing E. vaginatum and plots lacking vascular plants. Plots were located along a transect of increasing water table, in order to discriminate between the effects of E. vaginatum and the prevailing hydrological conditions on N2O fluxes. Net fluxes of N2O from the peat to the atmosphere were observed throughout the experimental area, as well as fluxes in the opposite direction, in which the peat removed N2O from the atmosphere inside the chamber. Non-zero fluxes were highly variable in both occurrence and magnitude, though a small number of plots accounted for the majority of measured fluxes. Neither aboveground biomass of E. vaginatum nor its presence in a plot was correlated with either frequency or direction of N2O flux measurements. Other factors, such as water table fluctuations and temperature may be stronger drivers of these microbially-mediated processes than vegetation at this stage of the

  14. Greenhouse gas fluxes (CO2, CH4, N2O) of a short-rotation poplar plantation after conversion from agriculture

    NASA Astrophysics Data System (ADS)

    Zona, D.; Janssens, I.; Aubinet, M.; Ceulemans, R.

    2012-12-01

    The increasing demand for renewable energy may lead to the conversion of millions of hectares into bioenergy plantations with a possible substantial transitory carbon (C) loss. Here we report on the greenhouse gas fluxes (CO2, CH4, and N2O) measured using eddy covariance of a short-rotation bioenergy poplar plantation converted from agricultural fields. The first six months after the establishment of the plantation (June-Dec 2010) presented substantial CO2, CH4, and N2O emissions (a total of 5.36 ± 0.52 Mg CO2eq ha-1 in terms of CO2 equivalents). Nitrous oxide loss mostly occurred during a week-long peak emission after an unusually large rainfall. This week-long N2O emission represented 52% of the entire N2O loss during one and an half years of measurements. As most of the N2O loss occurred in just this week-long period, accurately capturing these emission events are critical to accurate estimates of the GHG balance of bioenergy. While initial establishment (Jun-Dec 2010) of the plantation resulted in a net CO2 loss into the atmosphere (2.76 ± 0.16 Mg CO2eq ha-1), in the second year (2011) the plantation presented a substantial net CO2 uptake (-4.82 ± 0.47 Mg CO2eq ha-1). During the entire measurement period, CH4 was a source to the atmosphere (0.63 ± 0.05 Mg CO2eq ha-1 in 2010, and 0.49 ± 0.05 Mg CO2eq ha-1 in 2011), and was controlled by water table depth. Importantly, over the entire measurement period, the sum of the CH4 and N2O losses was almost double (3.51 ± 0.52 Mg CO2eq ha-1) than the magnitude of net CO2 uptake (-2.06 ± 0.50 Mg CO2eq ha-1). As water availability was an important control on the GHG emission of the plantation, expected climate change and altered rainfall pattern could increase the negative environmental impacts of bioenergy.

  15. High temporal resolution ecosystem CH4, CO2 and H2O flux data measured with a novel chamber technique

    NASA Astrophysics Data System (ADS)

    Steenberg Larsen, Klaus; Riis Christiansen, Jesper

    2016-04-01

    Soil-atmosphere exchange of greenhouse gases (GHGs) is commonly measured with closed static chambers (Pihlatie et al., 2013) with off-site gas chromatographic (GC) analysis for CH4 and N2O. Static chambers are widely used to observe in detail the effect of experimental manipulations, like climate change experiments, on GHG exchange (e.g. Carter et al., 2012). However, the low sensitivity of GC systems necessitates long measurement times and manual sampling, which increases the disturbance of the exchange of GHGs and leads to potential underestimation of fluxes (Christiansen et al., 2011; Creelman et al., 2013). The recent emergence of field proof infrared lasers using cavity ring-down spectroscopy (CRDS) have increased frequency and precision of concentration measurements and enabled better estimates of GHG fluxes (Christiansen et al., 2015) due to shorter chamber enclosure times. This minimizes the negative impact of the chamber enclosure on the soil-atmosphere gas exchange rate. Secondly, an integral aspect of understanding GHG exchange in terrestrial ecosystem is to achieve high temporal coverage. This is needed to capture the often dynamic behavior where fluxes can change rapidly over the course of days or even a few hours in response to e.g. rain events. Consequently, low temporal coverage in measurements of GHG exchange have in many past investigations led to highly uncertain annual budgets which severely limits our understanding of the ecosystem processes interacting with the climate system through GHG exchange. Real-time field measurements at high temporal resolution are needed to obtain a much more detailed understanding of the processes governing ecosystem CH4 exchange as well as for better predicting the effects of climate and environmental changes. We combined a state-of-the-art field applicable CH4 sensor (Los Gatos UGGA) with a newly developed ecosystem-level automatic chamber controlled by a LI-COR 8100/8150 system. The chamber is capable of

  16. Drivers of small scale variability in soil-atmosphere fluxes of CH4, N2O and CO2 in a forest soil

    NASA Astrophysics Data System (ADS)

    Maier, Martin; Nicolai, Clara; Wheeler, Denis; Lang, Friedeike; Paulus, Sinikka

    2016-04-01

    Soil-atmosphere fluxes of CH4, N2O and CO2 can vary on different spatial scales, on large scales between ecosystems but also within apparently homogenous sites. While CO2 and CH4 consumption is rather evenly distibuted in well aerated soils, the production of N2O and CH4 seems to occur at hot spots that can be associated with anoxic or suboxic conditions. Small-scale variability in soil properties is well-known from field soil assesment, affecting also soil aeration and thus theoretically, greenhouse gas fluxes. In many cases different plant species are associated with different soil conditions and vegetation mapping should therefor combined with soil mapping. Our research objective was explaining the small scale variability of greenhouse gas fluxes in an apparently homogeneous 50 years old Scots Pine stand in a former riparian flood plain.We combined greenhouse gas measurements and soil physical lab measurments with field soil assessment and vegetation mapping. Measurements were conducted with at 60 points at a plot of 30 X 30 m at the Hartheim monitoring site (SW Germany). For greenhouse gas measurements a non-steady state chamber system and laser analyser, and a photoacoustic analyser were used. Our study shows that the well aerated site was a substantial sink for atmospheric CH4 (-2.4 nmol/m² s) and also a for N2O (-0.4 nmol/m² s), but less pronounced, whereas CO2 production was a magnitude larger (2.6 μmol/m² s). The spatial variability of the CH4 consumption of the soils could be explained by the variability of the soil gas diffusivity (measured in situ + using soil cores). Deviations of this clear trend were only observed at points where decomposing woody debris was directly under the litter layer. Soil texture ranged from gravel, coarse sand, fine sand to pure silt, with coarser texture having higher soil gas diffusivity. Changes in texture were rather abrupt at some positions or gradual at other positions, and were well reflected in the vegetation

  17. Tree species influence soil-atmosphere fluxes of the greenhouse gases CO2, CH4 and N2O

    NASA Astrophysics Data System (ADS)

    Steffens, Christina; Vesterdal, Lars; Pfeiffer, Eva-Maria

    2016-04-01

    In the temperate zone, forests are the greatest terrestrial sink for atmospheric CO2, and tree species affect soil C stocks and soil CO2 emissions. When considering the total greenhouse gas (GHG) balance of the forest soil, the relevant GHGs CH4 and N2O should also be considered as they have a higher global warming potential than CO2. The presented data are first results from a field study in a common garden site in Denmark where tree species with ectomycorrhizal colonization (beech - Fagus sylvatica, oak - Quercus robur) and with arbuscular mycorrhizal colonization (maple - Acer pseudoplatanus, ash - Fraxinus excelsior) have been planted in monocultures in adjacent blocks of about 0.25 ha in the year 1973 on former arable land. The soil-atmosphere fluxes of all three gases were measured every second week since August 2015. The hypothesis is that the total GHG efflux from forest soil would differ between species, and that these differences could be related to the type of mycorrhizal association and leaf litter quality. Preliminary results (August to December 2015) indicate that tree species influence the fluxes (converted to CO2-eq) of the three GHGs. Total soil CO2 efflux was in the low end of the range reported for temperate broadleaved forests but similar to the measurements at the same site approximately ten years ago. It was highest under oak (9.6±2.4 g CO2 m-2 d-1) and lowest under maple (5.2±1.6 g CO2 m-2 d-1). In contrast, soil under oak was a small but significant sink for CH4(-0.005±0.003 g CO2-eq m-2 d-1), while there were almost no detectable CH4 fluxes in maple. Emissions of N2O were highest under beech (0.6±0.6 g CO2-eq m-2 d-1) and oak (0.2±0.09 g CO2-eq m-2 d-1) and lowest under ash (0.03±0.04 g CO2-eq m-2 d-1). In the total GHG balance, soil CH4 uptake was negligible (≤0.1% of total emissions). Emissions of N2O (converted to CO2-eq) contributed <1% (ash) to 8% (beech) to total GHG emissions. Summing up all GHG emissions, the tree species

  18. Effects of dairy manure management in annual and perennial cropping systems on soil microbial communities associated with in situ N2O fluxes

    NASA Astrophysics Data System (ADS)

    Dunfield, Kari; Thompson, Karen; Bent, Elizabeth; Abalos, Diego; Wagner-Riddle, Claudia

    2016-04-01

    Liquid dairy manure (LDM) application and ploughing events may affect soil microbial community functioning differently between perennial and annual cropping systems due to plant-specific characteristics stimulating changes in microbial community structure. Understanding how these microbial communities change in response to varied management, and how these changes relate to in situ N2O fluxes may allow the creation of predictive models for use in the development of best management practices (BMPs) to decrease nitrogen (N) losses through choice of crop, plough, and LDM practices. Our objectives were to contrast changes in the population sizes and community structures of genes associated with nitrifier (amoA, crenamoA) and denitrifier (nirK, nirS, nosZ) communities in differently managed annual and perennial fields demonstrating variation in N2O flux, and to determine if differences in these microbial communities were linked to the observed variation in N2O fluxes. Soil was sampled in 2012 and in 2014 in a 4-ha spring-applied LDM grass-legume (perennial) plot and two 4-ha corn (annual) treatments under fall or spring LDM application. Soil DNA was extracted and used to target N-cycling genes via qPCR (n=6) and for next-generation sequencing (Illumina Miseq) (n=3). Significantly higher field-scale N2O fluxes were observed in the annual plots compared to the perennial system; however N2O fluxes increased after plough down of the perennial plot. Nonmetric multidimensional scaling (NMS) indicated differences in N-cycling communities between annual and perennial cropping systems, and some communities became similar between annual and perennial plots after ploughing. Shifts in these communities demonstrated relationships with agricultural management, which were associated with differences in N2O flux. Indicator species analysis was used to identify operational taxonomic units (OTUs) most responsible for community shifts related to management. Nitrifying and denitrifying soil

  19. Comparisons between TiO2- and SiO2-flux assisted TIG welding processes.

    PubMed

    Tseng, Kuang-Hung; Chen, Kuan-Lung

    2012-08-01

    This study investigates the effects of flux compounds on the weld shape, ferrite content, and hardness profile in the tungsten inert gas (TIG) welding of 6 mm-thick austenitic 316 L stainless steel plates, using TiO2 and SiO2 powders as the activated fluxes. The metallurgical characterizations of weld metal produced with the oxide powders were evaluated using ferritoscope, optical microscopy, and Vickers microhardness test. Under the same welding parameters, the penetration capability of TIG welding with TiO2 and SiO2 fluxes was approximately 240% and 292%, respectively. A plasma column made with SiO2 flux exhibited greater constriction than that made with TiO2 flux. In addition, an anode root made with SiO2 flux exhibited more condensation than that made with TiO2 flux. Results indicate that energy density of SiO2-flux assisted TIG welding is higher than that of TiO2-flux assisted TIG welding.

  20. Comparison of N2O Emissions from Soils at Three Temperate Agricultural Sites

    NASA Technical Reports Server (NTRS)

    Frolking, S. E.; Moiser, A. R.; Ojima, D. S.; Li, C.; Parton, W. J.; Potter, C. S.; Priesack, E.; Stenger, R.; Haberbosch, C.; Dorsch, P.; hide

    1997-01-01

    Nitrous oxide (N2O) flux simulations by four models were compared with year-round field measurements from five temperate agricultural sites in three countries. The field sites included an unfertilized, semi-arid rangeland with low N2O fluxes in eastern Colorado, USA; two fertilizer treatments (urea and nitrate) on a fertilized grass ley cut for silage in Scotland; and two fertilized, cultivated crop fields in Germany where N2O loss during the winter was quite high. The models used were daily trace gas versions of the CENTURY model, DNDC, ExpertN, and the NASA-Ames version of the CASA model. These models included similar components (soil physics, decomposition, plant growth, and nitrogen transformations), but in some cases used very different algorithms for these processes. All models generated similar results for the general cycling of nitrogen through the agro-ecosystems, but simulated nitrogen trace gas fluxes were quite different. In most cases the simulated N20 fluxes were within a factor of about 2 of the observed annual fluxes, but even when models produced similar N2O fluxes they often produced very different estimates of gaseous N loss as nitric oxide (NO), dinitrogen (N2), and ammonia (NH3). Accurate simulation of soil moisture appears to be a key requirement for reliable simulation of N2O emissions. All models simulated the general pattern of low background fluxes with high fluxes following fertilization at the Scottish sites, but they could not (or were not designed to) accurately capture the observed effects of different fertilizer types on N2O flux. None of the models were able to reliably generate large pulses of N2O during brief winter thaws that were observed at the two German sites. All models except DNDC simulated very low N2O fluxes for the dry site in Colorado. The US Trace Gas Network (TRAGNET) has provided a mechanism for this model and site intercomparison. Additional intercomparisons are needed with these and other models and additional data

  1. Upland Trees Contribute to Exchange of Nitrous Oxide (N2O) in Forest Ecosystems

    NASA Astrophysics Data System (ADS)

    Tian, H.; Thompson, R.; Canadell, J.; Winiwarter, W.; Machacova, K.; Maier, M.; Halmeenmäki, E.; Svobodova, K.; Lang, F.; Pihlatie, M.; Urban, O.

    2017-12-01

    The increase in atmospheric nitrous oxide (N2O) concentration contributes to the acceleration of the greenhouse effect. However, the role of trees in the N2O exchange of forest ecosystems is still an open question. While the soils of temperate and boreal forests were shown to be a natural source of N2O, trees have been so far overlooked in the forest N2O inventories. We determined N2O fluxes in common tree species of boreal and temperate forests: Scots pine (Pinus sylvestris), Norway spruce (Picea abies), downy and silver birch (Betula pubescens, B. pendula), and European beech (Fagus sylvatica). We investigated (1) whether these tree species exchange N2O with the atmosphere under natural field conditions, (2) how the tree N2O fluxes contribute to the forest N2O balance, and (3) whether these fluxes show seasonal dynamics. The studies were performed in a boreal forest (SMEAR II station, Finland; June 2014 - May 2015) and two temperate mountain forests (White Carpathians, Czech Republic; Black Forest, Germany; June and July 2015). Fluxes of N2O in mature tree stems and forest floor were measured using static chamber systems followed by chromatographic and photo-acoustic analyses of N2O concentration changes. Pine, spruce and birch trees were identified as net annual N2O sources. Spruce was found the strongest emitter (0.27 mg ha-1 h-1) amounting thus up to 2.5% of forest floor N2O emissions. All tree species showed a substantial seasonality in stem N2O flux that was related to their physiological activity and climatic variables. In contrast, stems of beech trees growing at soils consuming N2O may act as a substantial sink of N2O from the atmosphere. Consistent N2O consumption by tree stems ranging between -12.1 and -35.2 mg ha-1 h-1 and contributing by up to 3.4% to the forest floor N2O uptake is a novel finding in contrast to current studies presenting trees as N2O emitters. To understand these fluxes, N2O exchange of photoautotrophic organisms associated with

  2. First on-line isotopic characterization of N2O above intensively managed grassland

    NASA Astrophysics Data System (ADS)

    Wolf, B.; Merbold, L.; Decock, C.; Tuzson, B.; Harris, E.; Six, J.; Emmenegger, L.; Mohn, J.

    2015-04-01

    The analysis of the four main isotopic N2O species (14N14N16O, 14N15N16O, 15N14N16O, 14N14N18O) and especially the intramolecular distribution of 15N ("site preference", SP) has been suggested as a tool to distinguish source processes and to help constrain the global N2O budget. However, current studies suffer from limited spatial and temporal resolution capabilities due to the combination of discrete flask sampling with subsequent laboratory-based mass-spectrometric analysis. Quantum cascade laser absorption spectroscopy (QCLAS) allows the selective high-precision analysis of N2O isotopic species at trace levels and is suitable for in situ measurements. Here, we present results from the first field campaign, conducted on an intensively managed grassland site in central Switzerland. N2O mole fractions and isotopic composition were determined in the atmospheric surface layer (at 2.2 m height) at a high temporal resolution with a modified state-of-the-art laser spectrometer connected to an automated N2O preconcentration unit. The analytical performance was determined from repeated measurements of a compressed air tank and resulted in measurement repeatability of 0.20, 0.12 and 0.11‰ for δ15Nα, δ15Nβ and δ18O, respectively. Simultaneous eddy-covariance N2O flux measurements were used to determine the flux-averaged isotopic signature of soil-emitted N2O. Our measurements indicate that, in general, nitrifier-denitrification and denitrification were the prevalent sources of N2O during the campaign and that variations in isotopic composition were due to alterations in the extent to which N2O was reduced to N2 rather than to other pathways, such as hydroxylamine oxidation. Management and rewetting events were characterized by low values of the intramolecular 15N site preference (SP), δ15Nbulk and δ18O, suggesting that nitrifier-denitrification and incomplete heterotrophic bacterial denitrification responded most strongly to the induced disturbances. The flux

  3. Effect of Rb2O and Cs2O on Inclusion Removal in 321 Stainless Steels Using Novel Basic Tundish Fluxes

    NASA Astrophysics Data System (ADS)

    Choi, Kyunsuk; Kang, Youngjo; Sohn, Il

    2016-06-01

    Inclusion removal and modification of the 321 stainless steel using Rb2O- and Cs2O-containing novel basic tundish flux has been investigated. The average inclusion diameter was significantly lowered after reaction of the liquid metal with the flux after 45 minutes in an induction furnace set at 1823 K (1550 °C) under an Ar atmosphere. The number of inclusions was also decreased with increased reaction time and the majority of the inherent TiN inclusions were removed after reaction with the proposed novel basic tundish flux. Spinel inclusions were also observed after the reaction, which was due to the reaction of the MgO crucible and the CaO-Al2O3-SiO2-MgO-` x'wt pct R2O flux system at fixed CaO/(Al2O3 + SiO2) of 1.45. The Rb2O and Cs2O seemed to have allowed significant removal of the TiN inclusions due to its ion compensation effect and the supplement of free oxygen ions, while increasing the viscosity of the slag to retain the absorbed inclusions.

  4. First on-line isotopic characterization of N2O emitted from intensively managed grassland

    NASA Astrophysics Data System (ADS)

    Wolf, B.; Merbold, L.; Decock, C.; Tuzson, B.; Harris, E.; Six, J.; Emmenegger, L.; Mohn, J.

    2015-01-01

    The analysis of the four main isotopic N2O species (14N14N16O, 14N15N16O, 15N14N16O, 14N14N18O) and especially the intramolecular distribution of 15N (site preference, SP) has been suggested as a tool to distinguish source processes and to help constrain the global N2O budget. However, current studies suffer from limited spatial and temporal resolution capabilities due to the combination of discrete flask sampling with subsequent laboratory-based mass spectrometric analysis. Quantum cascade laser absorption spectroscopy (QCLAS) allows selective high-precision analysis of N2O isotopic species at trace levels and is suitable for in situ measurements. Here, we present results from the first field campaign, conducted on an intensively managed grassland in central Switzerland. N2O mole fractions and isotopic composition were determined in the atmospheric surface layer (2 m height) at high temporal resolution with a modified state-of-the-art laser spectrometer connected to an automated N2O preconcentration unit. The analytical performance was determined from repeated measurements of a compressed air tank and resulted in measurement repeatability of 0.20, 0.12 and 0.11‰ for δ15Nα, δ15Nβ and δ18O, respectively. Simultaneous eddy-covariance N2O flux measurements were used to determine the flux-averaged isotopic signature of soil-emitted N2O. Our measurements indicate that in general, nitrifier-denitrification and denitrification were the prevalent sources of N2O during the campaign, and that variations in isotopic composition were rather due to alterations in the extent to which N2O was reduced to N2, than other pathways such as hydroxylamine oxidation. Management and rewetting events were characterized by low values of the intra-molecular 15N site preference (SP), δ15Nbulk and δ18O, suggesting nitrifier denitrification and incomplete heterotrophic bacterial denitrification responded most strongly to the induced disturbances. Flux-averaged isotopic composition of N

  5. Aircraft Observations of Nitrous Oxide (N2O) in the San Joaquin Valley of California

    NASA Astrophysics Data System (ADS)

    Muto, S.; Herrera, S.; Pusede, S.

    2017-12-01

    Agriculture is the largest source of anthropogenic nitrous oxide (N2O) in the U.S. While it is generally known which processes produce N2O, there is considerable uncertainty in controls over N2O emissions. Factors that determine N2O fluxes, such as soil properties and manure management, are highly variable in space and time, and, as a result, it has proven difficult to upscale chamber-derived soil flux measurements to regional spatial scales. Aircraft observations provide a regional picture of the N2O spatial distribution, but, because N2O is very long-lived, it is challenging to attribute measured concentrations of N2O to distinct local sources, especially over areas with complex and integrated land use. This study takes advantage of a novel aircraft N2O dataset collected onboard the low-flying, slow-moving NASA C-23 Sherpa in the San Joaquin Valley (SJV) of California, a region with a variety of N2O sources, including dairies, feedlots, fertilized cropland, and industrial facilities. With these measurements, we link observed N2O enhancements to specific sources at sub-inventory spatial scales. We compare our results with area-weighted emission profiles obtained by integrating detailed emission inventory data, agricultural statistics, and GIS source mapping.

  6. Diurnal variation of CO2, CH4, and N2O emission fluxes continuously monitored in-situ in three environmental habitats in a subtropical estuarine wetland.

    PubMed

    Yang, Wen-Bin; Yuan, Chung-Shin; Tong, Chuan; Yang, Pin; Yang, Lei; Huang, Bang-Qin

    2017-06-15

    Wetlands play a crucial role in modulating atmospheric concentrations of greenhouse gases (GHGs) such as carbon dioxide (CO 2 ), methane (CH 4 ), and nitrous oxide (N 2 O). The key factors controlling GHG emission from subtropical estuarine wetlands were investigated in this study, which continuously monitored the uptake/emission of GHGs (CO 2 , CH 4 , and N 2 O) by/from a subtropical estuarine wetland located in the Minjiang estuary in the coastal region of southeastern China. A self-designed floating chamber was used to collect air samples on-site at three environmental habitats (Phragmites australis marsh, mudflats, and river water). The CO 2 , CH 4 , and N 2 O concentrations were then measured using an automated nondispersive infrared analyzer. The magnitudes of the CO 2 and N 2 O emission fluxes at the three habitats were ordered as river water>P. australis>mudflats. P. australis emitted GHGs through photosynthesis and respiration processes. Emissions of CH 4 from P. australis and the mudflats were revealed to be slightly higher than those from the river water. The total GHG emission fluxes at the three environmental habitats were quite similar (4.68-4.78gm -2 h -1 ). However, when the total carbon dioxide equivalent fluxes (CO 2 -e) were considered, the river water was discovered to emit the most CO 2 -e compared with P. australis and the mudflats. Based on its potential to increase global warming, N 2 O was the main contributor to the total GHG emission, with that emitted from the river water being the most considerable. Tidal water carried onto the marsh had its own GHG content and thus has acted as a source or sink of GHGs. However, water quality had a large effect on GHG emissions from the river water whereas the tidal water height did not. Both high salinity and large amounts of sulfates in the wetlands explicitly inhibited the activity of CH 4 -producing bacteria, particularly at nighttime. Copyright © 2017 Elsevier Ltd. All rights reserved.

  7. High-accuracy measurements of N2O concentration and site-specific nitrogen isotopes in small or high concentration samples

    NASA Astrophysics Data System (ADS)

    Palmer, M. R.; Arata, C.; Huang, K.

    2014-12-01

    Nitrous oxide (N2O) gas is among the major contributors to global warming and ozone depletion in stratosphere. Quantitative estimate of N­2O production in various pathways and N­2O fluxes across different reservoirs is the key to understanding the role of N­2O in the global change. To achieve this goal, accurate and concurrent measurement of both N2O concentration ([N2O]) and its site-specific isotopic composition (SP-δ15N), namely δ15Nα and δ15Nβ, is desired. Recent developments in Cavity Ring-Down Spectroscopy (CRDS) have enabled high precision measurements of [N2O] and SP-δ15N of a continuous gas flow. However, many N­­2O samples are discrete with limited volume (< 500 ml), and/or high [N2O] (> 2 ppm), and are not suitable for direct measurements by CRDS. Here we present results of a Small Sample Isotope Module 2 (SSIM2) which is coupled to and automatically coordinated with a Picarro isotopic N2O CRDS analyzer to handle and measure high concentration and/or small volume samples. The SSIM2 requires 20 ml of sample per analysis, and transfers the sample to the CRDS for high precision measurement. When the sample injection is < 20 ml, a zero gas is optionally filled to make up the volume. We used the SSIM2 to dilute high [N2O] samples and < 20 ml samples, and tested the effect of dilution on the measured SP-δ15N. In addition, we employed and tested a newly developed double injection method for samples adequate for two 20 ml injections. After the SSIM2 and the CRDS cavity was primed with the first injection, the second injection, which has negligible dilution of the sample, can be accurately measured for both [N2O] and SP-δ15N. Results of these experiments indicate that the precision of SSIM2-CRDS is similar to that of the continuous measurements using the CRDS alone, and that dilution has minimal effect on SP-δ15N, as along as the [N2O] is > 300 ppb after dilution. Overall, the precision of SP-δ15N measured using the SSIM2 is < 0.5 ‰.

  8. Ocean N2O Emissions : Recent Global Estimates and Anthropogenically Influenced Changes

    NASA Astrophysics Data System (ADS)

    Suntharalingam, P.; Buithenuis, E.; Andrews, O.; Le Quere, C.

    2016-12-01

    models, and (iii) air-sea flux calculations which combine surface ocean N2O measurements with gas-exchange relationships. We will also present results from ongoing ocean biogeochemistry model analyses evaluating the separate influences of climate variation and anthropogenic nutrient inputs on ocean N2O emissions for recent decades.

  9. Global Flux Balance in the Terrestrial H2O Cycle: Reconsidering the Post-Arc Subducted H2O Flux

    NASA Astrophysics Data System (ADS)

    Parai, R.; Mukhopadhyay, S.

    2010-12-01

    Quantitative estimates of H2O fluxes between the mantle and the exosphere (i.e., the atmosphere, oceans and crust) are critical to our understanding of the chemistry and dynamics of the solid Earth: the abundance and distribution of water in the mantle has dramatic impacts upon mantle melting, degassing history, structure and style of convection. Water is outgassed from the mantle is association with volcanism at mid-ocean ridges, ocean islands and convergent margins. H2O is removed from the exosphere at subduction zones, and some fraction of the subducted flux may be recycled past the arc into the Earth’s deep interior. Estimates of the post-arc subducted H2O flux are primarily based on the stability of hydrous phases at subduction zone pressures and temperatures (e.g. Schmidt and Poli, 1998; Rüpke et al., 2004; Hacker, 2008). However, the post-arc H2O flux remains poorly quantified, in part due to large uncertainties in the water content of the subducting slab. Here we evaluate estimated post-arc subducted fluxes in the context of mantle-exosphere water cycling, using a Monte Carlo simulation of the global H2O cycle. Literature estimates of primary magmatic H2O abundances and magmatic production rates at different tectonic settings are used with estimates of the total subducted H2O flux to establish the parameter space under consideration. Random sampling of the allowed parameter space affords insight into which input and output fluxes satisfy basic constraints on global flux balance, such as a limit on sea-level change over time. The net flux of H2O between mantle and exosphere is determined by the total mantle output flux (via ridges and ocean islands, with a small contribution from mantle-derived arc output) and the input flux subducted beyond the arc. Arc and back-arc output is derived mainly from the slab, and therefore cancels out a fraction of the trench intake in an H2O subcycle. Limits on sea-level change since the end of the Archaean place

  10. Nitrous Oxide Emission Flux Measurements for Ecological Systems with an Open-Path Quantum Cascade Laser-Based Sensor

    NASA Astrophysics Data System (ADS)

    Tao, L.; Sun, K.; Cavigelli, M. A.; Gelfand, I.; Zenone, T.; Cui, M.; Miller, D. J.; Khan, M. A.; Zondlo, M. A.

    2012-12-01

    The ambient concentration of nitrous oxide (N2O), the fourth most abundant greenhouse gas, is rapidly increasing with emissions from both natural and anthropogenic sources [1]. Soil and aquatic areas are important sources and sinks for N2O due to complicated biogenic processes. However, N2O emissions are poorly constrained in space and time, despite its importance to global climate change and ozone depletion. We report our recent N2O emission measurements with an open-path quantum cascade laser (QCL)-based sensor for ecological systems. The newly emergent QCLs have been used to build compact, sensitive trace gas sensors in the mid-IR spectral region. A compact open-path QCL based sensor was developed to detect atmospheric N2O and CO at ~ 4.5 μm using wavelength modulation spectroscopy (WMS) to achieve a sensitivity of 0.26 ppbv of N2O and 0.24 ppbv of CO in 1 s with a power consumption of ~50 W [2]. This portable sensor system has been used to perform N2O emission flux measurement both with a static flux chamber and on an eddy covariance (EC) flux tower. In the flux chamber measurements, custom chambers were used to host the laser sensor, while gas samples for gas chromatograph (GC) were collected at the same time in the same chamber for validation and comparison. Different soil treatments have been applied in different chambers to study the relationship between N2O emission and the amount of fertilizer (and water) addition. Measurements from two methods agreed with each other (95% or higher confidence interval) for emission flux results, while laser sensor gave measurements with a much high temporal resolution. We have also performed the first open-path eddy covariance N2O flux measurement at Kellogg research station, Michigan State University for a month in June, 2012. Our sensor was placed on a 4-meter tower in a corn field and powered by batteries (connected with solar panels). We have observed the diurnal cycle of N2O flux. During this deployment, an inter

  11. Automated CO2, CH4 and N2O Fluxes from Tree Stems and Soils: Magnitudes, Temporal Patterns and Drivers

    NASA Astrophysics Data System (ADS)

    Barba, J.; Poyatos, R.; Vargas, R.

    2017-12-01

    The emissions of the main greenhouse gases (GHG; CO2, CH4 and N2O) through tree stems are still an uncertain component of the total GHG balance of forests. Despite that stem CO2 emissions have been studied for several decades, it is still unclear the drivers and spatiotemporal patterns of CH4 and N2O stem emissions. Additionally, it is unknown how stem emissions could be related to soil physiological processes or environmental conditions. We measured CO2, CH4 and N2O emissions hourly from April to July 2017 at two different heights (75 [LStem] and 150cm [HStem]) of bitternut hickory (Carya cordiformis) trees and adjacent soil locations in a forested area in the Mid Atlantic of the USA. We designed an automated system to continuously measure the three greenhouse gases (GHG) in stems and soils. Stem and soil CO2 emissions showed similar seasonal patterns with an average of 6.56±0.09 (soil), 3.72±0.05 (LStem) and 2.47±0.04 µmols m-2 s-1 (HStem) (mean±95% CI). Soil temperature controlled CO2 fluxes at both daily and seasonal scales (R2>0.5 for all cases), but there was no clear effect of soil moisture. The stems were a clear CH4 source with emissions decreasing with height (0.35±0.02 and 0.25±0.01 nmols m-2 s-1 for LStem and HStem, respectively) with no apparent seasonal pattern, and no clear relationship with environmental drivers (e.g., temperature, moisture). In contrast, soil was a CH4 sink throughout the experiment (-0.55±0.02 nmols m-2 s-1) and its seasonal pattern responded to moisture changes. Despite soil and stem N2O emissions did not show a seasonal pattern or apparent dependency on temperature or moisture, they showed net N2O emissions with a decrease in emissions with stem height (0.29±0.05 for soil, 0.38±0.06 for LStem and 0.28±0.05 nmols m-2 s-1 for HStem). The three GHG emissions decreased with stem height at similar rates (33%, 28% and 27% for CO2, CH4 and N2O, respectively). These results suggest that the gases were not produced in the stem

  12. Sunflower N2O emissions under two different water regimes in Mediterranean climate

    NASA Astrophysics Data System (ADS)

    Monaco, Eugenia; Vitale, Luca; Di Tommasi, Paul; Tedeschi, Anna; Tosca, Maurizio; Magliulo, Vincenzo

    2017-04-01

    Human activities are altering the atmospheric greenhouse gases (GHGs) concentration with negative effects on global climate and environment. Cropland represents about 12 % of earth's surface and largely contribute to GHGs production, in particular N2O, due to a massive use of nitrogen fertilization. In particular, agriculture and intensive livestock farming may significantly affect biogeochemical cycles included nitrogen cycle. However, it is often difficult to predict the total amount of fluxes caused by agricultural management, which impact on both the whole agro-ecosystem. The objective of the experiment was to evaluate soil N2O fluxes under two different irrigation managements. The experimental trial was conducted in a farm in surrounding of Naples, southern Italy. The crop monitored was sunflower for biomass uses. Two irrigation levels were performed: returning 100% (optimal irrigation) and 50% (deficit irrigation) of soil field capacity for the layer 0.0-0.50 m. 314 Kg ha-1 of urea fertilizer was supplied in two times: at sowing and 40 days later. Before sowing, six autochambers were inserted 3 cm into the soil and connected to a gas chromatograph and a scanning apparatus. A program for chambers' management was implemented to monitor soil N2O fluxes measured different times of the day. Biometric parameters such as LAI, root depth, above- and below-ground biomass were monitored during the experiment. Results shows that soil N2O fluxes were affected by irrigation regime; in particular, the deficit irrigation determined lower N2O fluxes compared to optimal irrigation but the total biomass production and yield were comparable between the two water regimes. So low input farm management could be take in account to reduce the total N2O emission and maintain at the same time high productivity level in terms of biomass and yield. Keywords: N2O fluxes, Irrigation schedule, sunflower

  13. Comparison of calculated and measured foliar O3 flux in crop and forest species

    Treesearch

    Nancy Grulke; E. Paoletti; R.L. Heath

    2007-01-01

    We designed a new gas exchange system that concurrently measures foliar H2O, O3, and CO2 flux (HOC flux system) while delivering known O3 concentrations. Stomatal responses of three species were tested: snapbean, and seedlings of California black oak (deciduous broadleaf) and...

  14. Multivariate regulation of soil CO2 and N2 O pulse emissions from agricultural soils.

    PubMed

    Liang, Liyin L; Grantz, David A; Jenerette, G Darrel

    2016-03-01

    Climate and land-use models project increasing occurrence of high temperature and water deficit in both agricultural production systems and terrestrial ecosystems. Episodic soil wetting and subsequent drying may increase the occurrence and magnitude of pulsed biogeochemical activity, affecting carbon (C) and nitrogen (N) cycles and influencing greenhouse gas (GHG) emissions. In this study, we provide the first data to explore the responses of carbon dioxide (CO2 ) and nitrous oxide (N2 O) fluxes to (i) temperature, (ii) soil water content as percent water holding capacity (%WHC), (iii) substrate availability throughout, and (iv) multiple soil drying and rewetting (DW) events. Each of these factors and their interactions exerted effects on GHG emissions over a range of four (CO2 ) and six (N2 O) orders of magnitude. Maximal CO2 and N2 O fluxes were observed in environments combining intermediate %WHC, elevated temperature, and sufficient substrate availability. Amendments of C and N and their interactions significantly affected CO2 and N2 O fluxes and altered their temperature sensitivities (Q10 ) over successive DW cycles. C amendments significantly enhanced CO2 flux, reduced N2 O flux, and decreased the Q10 of both. N amendments had no effect on CO2 flux and increased N2 O flux, while significantly depressing the Q10 for CO2 , and having no effect on the Q10 for N2 O. The dynamics across DW cycles could be attributed to changes in soil microbial communities as the different responses to wetting events in specific group of microorganisms, to the altered substrate availabilities, or to both. The complex interactions among parameters influencing trace gas fluxes should be incorporated into next generation earth system models to improve estimation of GHG emissions. © 2015 John Wiley & Sons Ltd.

  15. First real-time measurements of N2O isotopic signatures above intensively managed grassland: analytical performance, validation and illustrative examples

    NASA Astrophysics Data System (ADS)

    Wolf, Benjamin; Tuzson, Béla; Merbold, Lutz; Decock, Charlotte; Emmenegger, Lukas; Mohn, Joachim

    2014-05-01

    , and nitrate concentrations made the identification of controls on N2O isotopic composition possible. Furthermore, simultaneous eddy-covariance N2O flux measurements (Merbold et al. 2014) were used to derive a flux-averaged isotopic signature of soil-emitted N2O of intensively managed grassland. In this context, the potential of the derived N2O isotopic signatures for partitioning of microbial source processes will be discussed in relation to available literature data. Merbold, L, W Eugster, J Stieger, M Zahniser, D Nelson and N Buchmann. 2014. 'Greenhouse gas budget (CO2, CH4 and N2O) of intensively managed grassland following restoration' Global Change Biology doi:10.1111/gcb.12518 Mohn, J, B Tuzson, A Manninen, N Yoshida, S Toyoda, W A Brand, and L Emmenegger. 2012. 'Site selective real-time measurements of atmospheric N2O isotopomers by laser spectroscopy.' Atmospheric Measurement Techniques 5(7): 1601-1609 Park, S, P Croteau, K A Boering, D M Etheridge, D Ferretti, P J Fraser, K-R Kim, P B Krummel, R L Langenfelds, T D van Ommen, L P Steele, and C M Trudinger. 2012. 'Trends and seasonal cycles in the isotopic composition of nitrous oxide since 1940.' Nature Geoscience 5(4): 261-265. Waechter, H, J Mohn, B Tuzson, L Emmenegger, and M W Sigrist. 2008. 'Determination of N2O isotopomers with quantum cascade laser based absorption spectroscopy.' Optics Express 16(12): 9239-44. Wunderlin, P, M Lehmann, H Siegrist, B Tuzson, A Joss, L Emmenegger, and J Mohn. 2013. 'Isotope signatures of N2O in a mixed microbial population system: Constraints on N2O producing pathways in wastewater treatment.' Environmental Science and Technology 47: 1339-48.

  16. Distribution of flux-pinning energies in YBa2Cu3O(7-delta) and Bi2Sr2CaCu2O(8+delta) from flux noise

    NASA Astrophysics Data System (ADS)

    Ferrari, M. J.; Johnson, Mark; Wellstood, Frederick C.; Clarke, John; Mitzi, D.

    1990-01-01

    The spectral density of the magnetic flux noise measured in high-temperature superconductors in low magnetic fields scales approximately as the inverse of the frequency and increases with temperature. The temperature and frequency dependence of the noise are used to determine the pinning energies of individual flux vortices in thermal equilibrium. The distribution of pinning energies below 0.1 eV in YBa(2)Cu(3)O(7-delta) and near 0.2 eV in Bi(2)Sr(2)CaCu(2)O(8+delta). The noise power is proportional to the ambient magnetic field, indicating that the vortex motion is uncorrelated.

  17. Fluxes of the greenhouse gases (CO2, CH4 and N2O) above a short-rotation poplar plantation after conversion from agricultural land

    NASA Astrophysics Data System (ADS)

    Zona, Donatella; Ceulemans, Reinhart

    2013-04-01

    The increasing demand for renewable energy may lead to the conversion of millions of hectares into bioenergy plantations with a possible substantial transitory carbon (C) loss. In this study we report on the greenhouse gas fluxes (CO2, CH4, and N2O) measured using eddy covariance of a short-rotation bioenergy poplar plantation converted from agricultural fields. During the first six months after the establishment of the plantation (June-Dec 2010) there were substantial CO2, CH4, and N2O emissions (a total of 5.36 ± 0.52 Mg CO2eq ha-1 in terms of CO2 equivalents). Nitrous oxide loss mostly occurred during a week-long peak emission after an unusually large rainfall. This week-long N2O emission represented 52% of the entire N2O loss during one and an half years of measurements. As most of the N2O loss occurred in just this week-long period, accurately capturing these emission events are critical to accurate estimates of the GHG balance of bioenergy. While initial establishment (Jun-Dec 2010) of the plantation resulted in a net CO2 loss into the atmosphere (2.76 ± 0.16 Mg CO2eq ha-1), in the second year (2011) there was substantial net CO2 uptake (-3.51 ± 0.56 Mg CO2eq ha-1). During the entire measurement period, CH4 was a source to the atmosphere (0.63 ± 0.05 Mg CO2eq ha-1 in 2010, and 0.49 ± 0.05 Mg CO2eq ha-1 in 2011), and was controlled by water table depth. Importantly, over the entire measurement period, the sum of the CH4 and N2O losses was much higher (3.51 ± 0.52 Mg CO2eq ha-1) than the net CO2 uptake (-0.76 ± 0.58 Mg CO2eq ha-1). As water availability was an important control on the GHG emission of the plantation, expected climate change and altered rainfall pattern could increase the negative environmental impacts of bioenergy.

  18. Estimating N2O processes during grassland renewal and grassland conversion to maize cropping using N2O isotopocules

    NASA Astrophysics Data System (ADS)

    Buchen, Caroline; Well, Reinhard; Flessa, Heinz; Fuß, Roland; Helfrich, Mirjam; Lewicka-Szczebak, Dominika

    2017-04-01

    Grassland break-up due to grassland renewal and grassland conversion to cropland can lead to a flush of mineral nitrogen from decomposition of the old grass sward and the decomposition of soil organic matter. Moreover, increased carbon and nitrogen mineralisation can result in enhanced nitrous oxide (N2O) emissions. As N2O is known to be an important greenhouse gas and a major precursor for ozone depletion, its emissions need to be mitigated by adjusting agricultural management practices. Therefore, it is necessary to understand the N2O processes involved, as well as the contribution of N2O reduction to N2. Apart from the widely used 15N gas flux method, natural abundance isotopic analysis of the four most abundant isotopocules of N2O species is a promising alternative to assess N2O production pathways. We used stable isotope analyses of soil-emitted N2O (δ18ON2O, δ15NN2Obulk and δ15NN2OSP= intramolecular distribution of 15N within the linear N2O molecule) with an isotopocule mapping approach to simultaneously estimate the magnitude of N2O reduction to N2 and the fraction of N2O originating from the bacterial denitrification pathway or fungal denitrification and/or nitrification. This approach is based on endmember areas of isotopic values for the N2O produced from different sources reported in the literature. For this purpose, we calculated two main scenarios with different assumptions for N2O produced: N2O is reduced to N2 before residual N2O is mixed with N2O of various sources (Scenario a) and vice versa (Scenario b). Based on this, we applied seven different scenario variations, where we evaluated the range of possible values for the potential N2O production pathways (heterotrophic bacterial denitrification and/or nitrifier denitrification and fungal denitrification and/or nitrification). This was done by using a range of isotopic endmember values and assuming different fractionation factors of N2O reduction in order to find the most reliable scenario

  19. New gap-filling and partitioning technique for H2O eddy fluxes measured over forests

    NASA Astrophysics Data System (ADS)

    Kang, Minseok; Kim, Joon; Malla Thakuri, Bindu; Chun, Junghwa; Cho, Chunho

    2018-01-01

    The continuous measurement of H2O fluxes using the eddy covariance (EC) technique is still challenging for forests because of large amounts of wet canopy evaporation (EWC), which occur during and following rain events when the EC systems rarely work correctly. We propose a new gap-filling and partitioning technique for the H2O fluxes: a model-statistics hybrid (MSH) method. It enables the recovery of the missing EWC in the traditional gap-filling method and the partitioning of the evapotranspiration (ET) into transpiration and (wet canopy) evaporation. We tested and validated the new method using the data sets from two flux towers, which are located at forests in hilly and complex terrains. The MSH reasonably recovered the missing EWC of 16-41 mm yr-1 and separated it from the ET (14-23 % of the annual ET). Additionally, we illustrated certain advantages of the proposed technique which enable us to understand better how ET responds to environmental changes and how the water cycle is connected to the carbon cycle in a forest ecosystem.

  20. Effects of the fungicides mancozeb and chlorothalonil on fluxes of CO2, N2O, and CH4 in a fertilized Colorado grassland soil

    USGS Publications Warehouse

    Kinney, C.A.; Mosier, A.R.; Ferrer, I.; Furlong, E.T.; Mandernack, K.W.

    2004-01-01

    Management of agricultural soil plays an important role in present and future atmospheric concentrations of the greenhouse gases carbon dioxide (CO2), nitrous oxide (N2O), and methane (CH4). Pesticides are used as management tools in crop production, but little is known about their effects on soil-atmosphere exchange of CO2, N2O, and CH4. Field studies described in this paper determined the effect of two commonly used fungicides, mancozeb and chlorothalonil, on trace gas exchange. Separate experimental plots, 1 m2, were established in nitrogen fertilized no-tilled native grassland and tilled soils with and without fungicide application. Two studies were conducted. The first study was initiated in June 1999 and lasted for 1 year with monthly flux measurements from tilled and no-till soils. The second study commenced in August 2001 with twelve weekly measurements from tilled soils only. From both studies mancozeb suppressed emissions of CO2 and N2O in the tilled soil by an average of 28% and 47%, respectively. This suppression corresponded with efficacy periods of 14-29 and 56-77 days, respectively. From the no-till soils mancozeb decreased CO2 and N2O emissions by 33% and 80% for periods of 29 and 94 days, respectively. Mancozeb inhibited CH4 consumption in the first study by 46% and 71% in the tilled and no-till soil for periods of 8 and 29 days, respectively, but had no effect in the second study. From both studies chlorothalonil initially suppressed CO2 and N2O emissions and enhanced CH4 uptake in the tilled soil by an average of 37%, 40%, and 115%, respectively. These effects corresponded with efficacy periods of 14-29, 21-56, and 1-14 days, respectively. In the no-till soil chlorothalonil inhibited CO2 and N2O emissions and enhanced CH4 uptake by 29%, 48%, and 86% for periods of 29, 56, and 56 days, respectively. Following the initial period of suppression, chlorothalonil subsequently enhanced N2O emissions in the tilled soil by an average of 51% and in the no

  1. [Effects of diurnal warming on soil N2O emission in soybean field].

    PubMed

    Hu, Zheng-Hua; Zhou, Ying-Ping; Cui, Hai-Ling; Chen, Shu-Tao; Xiao, Qi-Tao; Liu, Yan

    2013-08-01

    To investigate the impact of experimental warming on N2O emission from soil of soybean field, outdoor experiments with simulating diurnal warming were conducted, and static dark chamber-gas chromatograph method was used to measure N2O emission fluxes. Results indicated that: the diurnal warming did not change the seasonal pattern of N2O emissions from soil. In the whole growing season, comparing to the control treatment (CK), the warming treatment (T) significantly enhanced the N2O flux and the cumulative amount of N2O by 17.31% (P = 0.019), and 20.27% (P = 0.005), respectively. The significant correlations were found between soil N2O emission and soil temperature, moisture. The temperature sensitivity values of soil N2O emission under CK and T treatments were 3.75 and 4.10, respectively. In whole growing stage, T treatment significantly increased the crop aboveground and total biomass, the nitrate reductase activity, and total nitrogen in leaves, while significantly decreased NO3(-) -N content in leaves. T treatment significantly increased soil NO3(-) -N content, but had no significant effect on soil organic carbon and total nitrogen contents. The results of this study suggested that diurnal warming enhanced N2O emission from soil in soybean field.

  2. Closed-loop 15N measurement of N2O and its isotopomers for real-time greenhouse gas tracing

    NASA Astrophysics Data System (ADS)

    Slaets, Johanna; Mayr, Leopold; Heiling, Maria; Zaman, Mohammad; Resch, Christian; Weltin, Georg; Gruber, Roman; Dercon, Gerd

    2016-04-01

    Quantifying sources of nitrous oxide is essential to improve understanding of the global N cycle and to develop climate-smart agriculture, as N2O has a global warming potential 300 times higher than CO2. The isotopic signature and the intramolecular distribution (site preference) of 15N are powerful tools to trace N2O, but the application of these methods is limited as conventional methods cannot provide continuous and in situ data. Here we present a method for closed-loop, real time monitoring of the N2O flux, the isotopic signature and the intramolecular distribution of 15N by using off-axis integrated cavity output spectroscopy (ICOS, Los Gatos Research). The developed method was applied to a fertilizer inhibitor experiment, in which N2O emissions were measured on undisturbed soil cores for three weeks. The treatments consisted of enriched urea-N (100 kg urea-N/ha), the same fertilizer combined with the nitrification inhibitor nitrapyrin (375 g/100 kg urea), and control cores. Monitoring the isotopic signature makes it possible to distinguish emissions from soil and fertilizer. Characterization of site preference could additionally provide a tool to identify different microbial processes leading to N2O emissions. Furthermore, the closed-loop approach enables direct measurement on site and does not require removal of CO2 and H2O. Results showed that 75% of total N2O emissions (total=11 346 μg N2O-N/m2) in the fertilized cores originated from fertilizer, while only 55% of total emissions (total=2 450 μg N2ON/m2) stemmed from fertilizer for the cores treated with nitrapyrin. In the controls, N2O derived from soil was only 40% of the size of the corresponding pool from the fertilized cores, pointing towards a priming effect on the microbial community from the fertilizer and demonstrating the bias that could be introduced by relying on non-treated cores to estimate soil emission rates, rather than using the isotopic signature. The site preference increased linearly

  3. Annual N2O emissions from conventionally grazed typical alpine grass meadows in the eastern Qinghai-Tibetan Plateau.

    PubMed

    Zhang, Han; Yao, Zhisheng; Wang, Kai; Zheng, Xunhua; Ma, Lei; Wang, Rui; Liu, Chunyan; Zhang, Wei; Zhu, Bo; Tang, Xiangyu; Hu, Zhenghua; Han, Shenghui

    2018-06-01

    Annual nitrous oxide (N 2 O) emissions from high-altitude alpine meadow grasslands have not been effectively characterized because of the scarcity of whole-year measurements. The authors performed a year-round measurement of N 2 O fluxes from three conventionally grazed alpine meadows that represent the typical meadow landscape in the eastern Qinghai-Tibetan Plateau (QTP). The results showed that annual N 2 O emissions averaged 0.123±0.053 (2SD, i.e., the double standard deviation indicating the 95% confidence interval) kgNha -1 yr -1 across the three meadow sites. N 2 O flux pulses during the spring freezing-thawing period (FTP) were observed at only one site, indicating a large spatial variability in association with soil moisture differences. Approximately 34-57% (mean: 46%) of the annual N 2 O emissions occurred in the non-growing season, highlighting the substantial importance of accurate flux observations during this period. The simultaneous observations showed conservative, marginal nitric oxide (NO) fluxes of 0.058±0.032 (2SD) kgNha -1 yr -1 . The N 2 O fluxes across the three field sites correlated negatively with the soil nitrate concentrations during the entire year-round period (P<0.05). Furthermore, a significant joint regulatory effect of topsoil temperature and moisture on the N 2 O and NO fluxes was observed during the relatively warm periods. Based on the results of the present and previous studies, a simple extrapolation roughly estimated the annual total N 2 O emission from Chinese grasslands to be 73±15 (2SD) GgNyr -1 (1Gg=10 9 g). A linear dependence of the annual N 2 O fluxes on the aboveground net primary productivity (ANPP) was also found. This result may provide a simple approach for estimating the N 2 O emission inventories of frigid alpine or temperate grasslands that are ungrazed either in the summer or year round. However, further confirmation of this relationship with a wider ANPP range is still needed in the future studies

  4. Influence of biomass harvesting on fluxes of CO2 CH4 and N2O for a sedge fen in south-west Belarus

    NASA Astrophysics Data System (ADS)

    Burlo, A.; Minke, M.; Chuvashova, H.; Yarmashuk, T.; Augustin, J.; Thiele, A.; Tichonov, V.; Liashchynskaya, N.; Narkevitch, I.

    2012-04-01

    Until now, it is usual to drain a peatland to be able to use it economically. The consequences are a progressive peat loss and a negative climate impact caused by a strong emission of the greenhouse gases CO2 and N2O (Droesler et al., 2008). To avoid these negative effects of the peatland use, the concept of the so-called Paludiculture was developed. This is the harvest of plant biomass on wet and rewetted peatlands (Wichtmann & Joosten 2007). However, there is only few and contradictory information about the actual effect of the Paludiculture on the greenhouse gas fluxes, the peat carbon budget, and the climate balance so far. Therefore, we investigated the influence of late mowing on a sedge fen in the Paliessie region in SW Belarus. The site is characterized by Carex nigra, Carex rostrata, Calamagrostis canescens, Potentilla palustris, Drepanocladus aduncus and Rhizomnium punctatum and a mean water level close to the surface. The investigation covers two variants: Without use (control), and the removal of the aboveground biomass in late autumn. For every variant, we installed three soil collars distributed randomly as a base for the gas flux measurements. Since August 2010 the CO2, CH4 and N2O exchange rates are measured by the closed chamber approach of Droesler (2005). The first harvest of plant biomass was on 17th of November 2010. It turned out, that the single gas fluxes are influenced very differently by the biomass removal. In case of the CH4 a noticeable impact of mowing became evident directly after melting of the ice layer in spring 2011, when the emissions at the harvested plots for nearly doubled those from the control on two measurement campaigns. The N2O fluxes were very week but these are according to tendency lower on the harvest variant all the time. However, the ecosystem respiration did not show any clear reaction on the mowing at all. Furthermore, we will report about the effects of the biomass removal on the current net CO2 exchange, the

  5. Intercomparison of fast response commercial gas analysers for nitrous oxide flux measurements under field conditions

    NASA Astrophysics Data System (ADS)

    Rannik, Ü.; Haapanala, S.; Shurpali, N. J.; Mammarella, I.; Lind, S.; Hyvönen, N.; Peltola, O.; Zahniser, M.; Martikainen, P. J.; Vesala, T.

    2015-01-01

    Four gas analysers capable of measuring nitrous oxide (N2O) concentration at a response time necessary for eddy covariance flux measurements were operated from spring until winter 2011 over a field cultivated with reed canary grass (RCG, Phalaris arundinacea, L.), a perennial bioenergy crop in eastern Finland. The instruments were TGA100A (Campbell Scientific Inc.), CW-TILDAS-CS (Aerodyne Research Inc.), N2O / CO-23d (Los Gatos Research Inc.) and QC-TILDAS-76-CS (Aerodyne Research Inc.). The period with high emissions, lasting for about 2 weeks after fertilization in late May, was characterized by an up to 2 orders of magnitude higher emission, whereas during the rest of the campaign the N2O fluxes were small, from 0.01 to 1 nmol m-2 s-1. Two instruments, CW-TILDAS-CS and N2O / CO-23d, determined the N2O exchange with minor systematic difference throughout the campaign, when operated simultaneously. TGA100A produced the cumulatively highest N2O estimates (with 29% higher values during the period when all instruments were operational). QC-TILDAS-76-CS obtained 36% lower fluxes than CW-TILDAS-CS during the first period, including the emission episode, whereas the correspondence with other instruments during the rest of the campaign was good. The reasons for systematic differences were not identified, suggesting further need for detailed evaluation of instrument performance under field conditions with emphasis on stability, calibration and any other factors that can systematically affect the accuracy of flux measurements. The instrument CW-TILDAS-CS was characterized by the lowest noise level (with a standard deviation of around 0.12 ppb at 10 Hz sampling rate) as compared to N2O / CO-23d and QC-TILDAS-76-CS (around 0.50 ppb) and TGA100A (around 2 ppb). We identified that for all instruments except CW-TILDAS-CS the random error due to instrumental noise was an important source of uncertainty at the 30 min averaging level and the total stochastic error was frequently

  6. Inhibition effect of zinc in wastewater on the N2O emission from coastal loam soils.

    PubMed

    Huang, Yan; Ou, Danyun; Chen, Shunyang; Chen, Bin; Liu, Wenhua; Bai, Renao; Chen, Guangcheng

    2017-03-15

    The effects of zinc (Zn) on nitrous oxide (N 2 O) fluxes from coastal loam soil and the abundances of soil nitrifier and denitrifier were studied in a tidal microcosm receiving livestock wastewater with different Zn levels. Soil N 2 O emission significantly increased due to discharge of wastewater rich in ammonia (NH 4 + -N) while the continuous measurements of gas flux showed a durative reduction in N 2 O flux by high Zn input (40mgL -1 ) during the low tide period. Soil inorganic nitrogen concentrations increased at the end of the experiment and even more soil NH 4 + -N was measured in the high-Zn-level treatment, indicating an inhibition of ammonia oxidation by Zn input. Quantitative PCR of soil amoA, narG and nirK genes encoding ammonia monooxygenase, nitrate reductase and nitrite reductase, respectively, showed that the microbial abundances involved in these metabolisms were neither affected by wastewater discharge nor Zn contamination. Copyright © 2017 Elsevier Ltd. All rights reserved.

  7. Frozen Cropland Soil in Northeast China as Source of N2O and CO2 Emissions

    PubMed Central

    Qiao, Yunfa; Han, Xiaozeng; Brancher Franco, Roberta

    2014-01-01

    Agricultural soils are important sources of atmospheric N2O and CO2. However, in boreal agro-ecosystems the contribution of the winter season to annual emissions of these gases has rarely been determined. In this study, soil N2O and CO2 fluxes were measured for 6 years in a corn-soybean-wheat rotation in northeast China to quantify the contribution of wintertime N2O and CO2 fluxes to annual emissions. The treatments were chemical fertilizer (NPK), chemical fertilizer plus composted pig manure (NPKOM), and control (Cont.). Mean soil N2O fluxes among all three treatments in the winter (November–March), when soil temperatures are below −7°C for extended periods, were 0.89–3.01 µg N m−2 h−1, and in between the growing season and winter (October and April), when freeze-thaw events occur, 1.73–5.48 µg N m−2 h−1. The cumulative N2O emissions were on average 0.27–1.39, 0.03–0.08 and 0.03–0.11 kg N2O–N ha−1 during the growing season, October and April, and winter, respectively. The average contributions of winter N2O efflux to annual emissions were 6.3–12.1%. In all three seasons, the highest N2O emissions occurred in NPKOM, while NPK and Cont. emissions were similar. Cumulative CO2 emissions were 2.73–4.94, 0.13–0.20 and 0.07–0.11 Mg CO2-C ha−1 during growing season, October and April, and winter, respectively. The contribution of winter CO2 to total annual emissions was 2.0–2.4%. Our results indicate that in boreal agricultural systems in northeast China, CO2 and N2O emissions continue throughout the winter. PMID:25536036

  8. Isotopomer and isotopologue signatures of N2O produced in alpine ecosystems on the Qinghai-Tibetan Plateau.

    PubMed

    Kato, Tomomichi; Toyoda, Sakae; Yoshida, Naohiro; Tang, Yanhong; Wada, Eitaro

    2013-07-15

    Static-chamber flux measurements have suggested that one of the world's largest grasslands, the Qinghai-Tibetan Plateau (QTP), is a potential source of nitrous oxide (N2O), a major greenhouse gas. However, production and consumption pathways of N2O have not been identified by in situ field measurements. Ratios of N2O isotopomers ((14)N(15)N(16)O and (15)N(14)N(16)O) and an isotopologue ((14)N(14)N(18)O) with respect to (14)N(14)N(16)O in the atmosphere, static chambers, and soils were measured by gas chromatography and mass spectrometry in the summer of 2005 and the following winter of 2006 at three typical alpine ecosystems: alpine meadow, alpine shrub, and alpine wetland, on the QTP, China. Site preference (SP) values of soil-emitted N2 O were estimated as 33.7‰ and 30.1‰ for alpine meadow and shrub, respectively, suggesting larger contributions by fungal denitrification, than by bacterial denitrification and nitrifier-denitrification, to N2 O production. Statistical analysis of the relationship between SP and δ(15)N(bulk) values indicated that in alpine meadow, shrub, and wetland sites fungal denitrification contributed 40.7%, 40.0%, and 23.2% to gross N2O production and the produced N2O was reduced by 87.6%, 82.9%, and 92.7%, respectively. The combined measurements of N2O concentration, flux, and isotopomeric signatures provide a robust estimation of N2O circulation dynamics in alpine ecosystems on the QTP, which would contribute to the development of ecosystem nitrogen cycle model. Copyright © 2013 John Wiley & Sons, Ltd.

  9. The denitrification paradox: The role of O2 in sediment N2O production

    NASA Astrophysics Data System (ADS)

    Barnes, Jonathan; Upstill-Goddard, Robert C.

    2018-01-01

    We designed a novel laboratory sediment flux chamber in which we maintained the headspace O2 partial pressure at preselected values, allowing us to experimentally regulate "in-situ" O2 to evaluate its role in net N2O production by an intertidal estuarine sediment (Tyne, UK). In short-term (30 h) incubations with 10 L of overlying estuarine water (∼3 cm depth) and headspace O2 regulation (headspace: sediment/water ratio ∼9:1), net N2O production was highest at 1.2% O2 (sub-oxic; 32.3 nmol N2O m-2 d-1), an order of magnitude higher than at either 0.0% (anoxic; 2.5 N2O nmol m-2 d-1) or 20.85% (ambient; 2.3 nmol N2O m-2 d-1) O2. In a longer-term sealed incubation (∼490 h) without O2 control, time-dependent behaviour of N2O in the tank headspace was highly non-linear with time, showing distinct phases: (i) an initial period of no or little change in O2 or N2O up to ∼ 100 h; (ii) a quasi-linear, inverse correlation between O2 and N2O to ∼360 h, in which O2 declined to ∼2.1% and N2O rose to ∼7800 natm; (iii) over the following 50 h a slower O2 decline, to ∼1.1%, and a more rapid N2O increase, to ∼12000 natm; (iv) over the next 24 h a slowed O2 decline towards undetectable levels and a sharp fall in N2O to ∼4600 natm; (iv) a continued N2O decrease at zero O2, to ∼3000 natm by ∼ 490 h. These results show clearly that rapid N2O consumption (∼115 nmol m-2 d-1), presumably via heterotrophic denitrification (HD), occurs under fully anoxic conditions and therefore that N2O production, which was optimal for sub-oxic O2, results from other nitrogen transformation processes. In experiments in which we amended sediment overlying water to either 1 mM NH4+ or 1 mM NO3-, N2O production rates were 2-134 nmol N2O m-2 d-1 (NH4+ addition) and 0.4-2.2 nmol N2O m-2 d-1 (NO3- addition). We conclude that processes involving NH4+ oxidation (nitrifier nitrification; nitrifier denitrification; nitrification-coupled denitrification) are principally responsible for N2O

  10. Subtask 1.22 - Microbial Cycling of CH4, CO2, and N2O in a Wetlands Environment

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    Dingyi Ye; Bethany Kurz; Marc Kurz

    Soil microbial metabolic activities play an important role in determining CO{sub 2}, CH{sub 4}, and N{sub 2}O fluxes from terrestrial ecosystems. To verify and evaluate CO{sub 2} sequestration potential by wetland restoration in the Prairie Pothole Region (PPR), as well as to address concern over restoration effects on CH{sub 4} and N{sub 2}O emissions, laboratory and in situ microcosm studies on microbial cycling of CO{sub 2}, CH{sub 4}, and N{sub 2}O were initiated. In addition, to evaluate the feasibility of the use of remote sensing to detect soil gas flux from wetlands, a remote-sensing investigation was also conducted. Results ofmore » the laboratory microcosm study unequivocally proved that restoration of PPR wetlands does sequester atmospheric CO{sub 2}. Under the experimental conditions, the simulated restored wetlands did not promote neither N{sub 2}O nor CH{sub 4} fluxes. Application of ammonia enhanced both N{sub 2}O and CH{sub 4} emission, indicating that restoration of PPR wetlands may reduce both N{sub 2}O and CH{sub 4} emission by cutting N-fertilizer input. Enhancement of CO{sub 2} emission by the N-fertilizer was observed, and this observation revealed an overlooked fact that application of N-fertilizer may potentially increase CO{sub 2} emission. In addition, the CO{sub 2} results also demonstrate that wetland restoration sequesters atmospheric carbon not only by turning soil conditions from aerobic to anoxic, but also by cutting N-fertilizer input that may enhance CO{sub 2} flux. The investigation on microbial community structure and population dynamics showed that under the experimental conditions restoration of the PPR wetlands would not dramatically increase population sizes of those microorganisms that produce N{sub 2}O and CH{sub 4}. Results of the in situ study proved that restoration of the PPR wetland significantly reduced CO{sub 2} flux. Ammonia enhanced the greenhouse gas emission and linearly correlated to the CO{sub 2} flux within

  11. Characterization of remote O2-plasma-enhanced CVD SiO2/GaN(0001) structure using photoemission measurements

    NASA Astrophysics Data System (ADS)

    Truyen, Nguyen Xuan; Ohta, Akio; Makihara, Katsunori; Ikeda, Mitsuhisa; Miyazaki, Seiichi

    2018-01-01

    The control of chemical composition and bonding features at a SiO2/GaN interface is a key to realizing high-performance GaN power devices. In this study, an ∼5.2-nm-thick SiO2 film has been deposited on an epitaxial GaN(0001) surface by remote O2-plasma-enhanced chemical vapor deposition (O2-RPCVD) using SiH4 and Ar/O2 mixture gases at a substrate temperature of 500 °C. The depth profile of chemical structures and electronic defects of the O2-RPCVD SiO2/GaN structures has been evaluated from a combination of SiO2 thinning examined by X-ray photoelectron spectroscopy (XPS) and the total photoelectron yield spectroscopy (PYS) measurements. As a highlight, we found that O2-RPCVD is effective for fabricating an abrupt SiO2/GaN interface.

  12. The effects of nitrogen fertilization on N2O emissions from a rubber plantation

    NASA Astrophysics Data System (ADS)

    Zhou, Wen-Jun; Ji, Hong-Li; Zhu, Jing; Zhang, Yi-Ping; Sha, Li-Qing; Liu, Yun-Tong; Zhang, Xiang; Zhao, Wei; Dong, Yu-Xin; Bai, Xiao-Long; Lin, You-Xin; Zhang, Jun-Hui; Zheng, Xun-Hua

    2016-06-01

    To gain the effects of N fertilizer applications on N2O emissions and local climate change in fertilized rubber (Hevea brasiliensis) plantations in the tropics, we measured N2O fluxes from fertilized (75 kg N ha-1 yr-1) and unfertilized rubber plantations at Xishuangbanna in southwest China over a 2-year period. The N2O emissions from the fertilized and unfertilized plots were 4.0 and 2.5 kg N ha-1 yr-1, respectively, and the N2O emission factor was 1.96%. Soil moisture, soil temperature, and the area weighted mean ammoniacal nitrogen (NH4+-N) content controlled the variations in N2O flux from the fertilized and unfertilized rubber plantations. NH4+-N did not influence temporal changes in N2O emissions from the trench, slope, or terrace plots, but controlled spatial variations in N2O emissions among the treatments. On a unit area basis, the 100-year carbon dioxide equivalence of the fertilized rubber plantation N2O offsets 5.8% and 31.5% of carbon sink of the rubber plantation and local tropical rainforest, respectively. When entire land area in Xishuangbanna is considered, N2O emissions from fertilized rubber plantations offset 17.1% of the tropical rainforest’s carbon sink. The results show that if tropical rainforests are converted to fertilized rubber plantations, regional N2O emissions may enhance local climate warming.

  13. Measuring hourly 18O and 2H fluxes in a mixed hardwood forest using an integrated cavity output spectrometer

    NASA Astrophysics Data System (ADS)

    Wang, L.; Caylor, K.; Dragoni, D.

    2008-12-01

    The 18O and 2H of water vapor can be used to investigate couplings between biological processes (e.g., photosynthesis or transpiration) and hydrologic processes (e.g., evaporation) and therefore serve as powerful tracers in hydrological cycles. A typical method for determining δ18O and δ2H fluxes in landscapes is a 'Keeling Plot' approach, which uses field-collected vapor samples coupled with a traditional isotope ratio mass spectrometer to infer the isotopic composition of evapotranspiration. However, fractionation accompanying inefficient vapor trapping can lead to large measurement uncertainty and the intensive laboring involved in cold-trap make it almost impossible for continuous measurements. Over the last 3-4 years a few groups have developed continuous approaches for measuring δ18O and δ2H that use laser absorption spectroscopy (LAS) to achieve accuracy levels similar to lab-based mass spectrometry methods. Unfortunately, most LAS systems need cryogenic cooling, constant calibration to a reference gas, and substantial power requirements, which make them unsuitable for long-term field deployment at remote field sites. In this research, we tested out a new LAS--based water vapor isotope analyzer (WVIA, Los Gatos Research, Inc, Mountain View, CA) based on Integrated Cavity Output Spectroscopy (ICOS) and coupled this instrument with a flux gradient system. The WVIA was calibrated bi- weekly using a dew point generator and water with known δ18O and δ2H signatures. The field work was performed at Morgan-Monroe State Forest Ameriflux tower site (central Indiana) between August 8 and August 27, 2008. The combination method was able to produce hourly δ18O and δ2H fluxes data with reproducibility similar to lab-based mass spectrometry methods. Such high temporal resolution data were also able to capture signatures of canopy and bare soil evaporation to individual rainfall events. The use of the ICOS water vapor analyzer within a gradient system has the

  14. Conversion from rice to vegetable production increases N2O emission via increased soil organic matter mineralization.

    PubMed

    Wu, Lei; Tang, Shuirong; He, Dongdong; Wu, Xian; Shaaban, Muhammad; Wang, Milan; Zhao, Jingsong; Khan, Imran; Zheng, Xunhua; Hu, Ronggui; Horwath, William R

    2017-04-01

    The conversion from rice to vegetable production widely occurs in China. However, the effects of this conversion on N 2 O emission and the underlying mechanisms are not well understood. In the present study, 12 rice paddies (R) were selected and half of them converted to vegetable fields (V) with the following treatments: rice paddies without N-fertilizer (R-CK), rice paddies with conventional N-fertilizer (R-CN), converted vegetable fields without N-fertilizer (V-CK), and converted vegetable fields with conventional N-fertilizer (V-CN) in a randomized block design with 3 replicates. N 2 O emissions were measured with static chambers from December 2012 to December 2015. Within each V-CN plot, a root exclusion subplot was established to measure soil heterotrophic respiration (CO 2 effluxes), a proxy for soil organic matter mineralization. Conversion of rice paddies to vegetable production dramatically increased N 2 O emissions. The three-year cumulative N 2 O emissions were 0.59, 1.90, 55.50 and 160.14kg N ha -1 for R-CK, R-CN, V-CK and V-CN, respectively. The annual N 2 O emissions from vegetable fields ranged between 5.99 and 113.45kg N ha -1 yr -1 , with substantially higher emissions in the first year. N 2 O fluxes from V-CN were significantly and positively related to CO 2 fluxes and inorganic N concentrations. The linear relationship between natural logarithms of N 2 O and CO 2 fluxes was stronger and the regression coefficient higher in the first year, showing the dependence of N 2 O on soil organic matter mineralization. These results suggest that soil organic matter and N mineralization contributes significantly to N 2 O emission following conversion of rice paddies to vegetable production. Copyright © 2017 Elsevier B.V. All rights reserved.

  15. Isotope signatures of N2O emitted from vegetable soil: Ammonia oxidation drives N2O production in NH4(+)-fertilized soil of North China.

    PubMed

    Zhang, Wei; Li, Yuzhong; Xu, Chunying; Li, Qiaozhen; Lin, Wei

    2016-07-08

    Nitrous oxide (N2O) is a potent greenhouse gas. In North China, vegetable fields are amended with high levels of N fertilizer and irrigation water, which causes massive N2O flux. The aim of this study was to determine the contribution of microbial processes to N2O production and characterize isotopic signature effects on N2O source partitioning. We conducted a microcosm study that combined naturally abundant isotopologues and gas inhibitor techniques to analyze N2O flux and its isotopomer signatures [δ(15)N(bulk), δ(18)O, and SP (intramolecular (15)N site preference)] that emitted from vegetable soil after the addition of NH4(+) fertilizers. The results show that ammonia oxidation is the predominant process under high water content (70% water-filled pore space), and nitrifier denitrification contribution increases with increasing N content. δ(15)N(bulk) and δ(18)O of N2O may not provide information about microbial processes due to great shifts in precursor signatures and atom exchange, especially for soil treated with NH4(+) fertilizer. SP and associated two end-member mixing model are useful to distinguish N2O source and contribution. Further work is needed to explore isotopomer signature stability to improve N2O microbial process identification.

  16. Short-term nitrogen additions can shift a coastal wetland from a sink to a source of N2O

    USGS Publications Warehouse

    Moseman-Valtierra, Serena; Gonzalez, Rosalinda; Kroeger, Kevin D.; Tang, Jianwu; Chao, Wei Chun; Crusius, John; Bratton, John F.; Green, Adrian; Shelton, James

    2011-01-01

    Coastal salt marshes sequester carbon at high rates relative to other ecosystems and emit relatively little methane particularly compared to freshwater wetlands. However, fluxes of all major greenhouse gases (N2O, CH4, and CO2) need to be quantified for accurate assessment of the climatic roles of these ecosystems. Anthropogenic nitrogen inputs (via run-off, atmospheric deposition, and wastewater) impact coastal marshes. To test the hypothesis that a pulse of nitrogen loading may increase greenhouse gas emissions from salt marsh sediments, we compared N2O, CH4 and respiratory CO2fluxes from nitrate-enriched plots in a Spartina patens marsh (receiving single additions of NaNO3 equivalent to 1.4 g N m−2) to those from control plots (receiving only artificial seawater solutions) in three short-term experiments (July 2009, April 2010, and June 2010). In July 2009, we also compared N2O and CH4 fluxes in both opaque and transparent chambers to test the influence of light on gas flux measurements. Background fluxes of N2O in July 2009 averaged −33 μmol N2O m−2 day−1. However, within 1 h of nutrient additions, N2O fluxes were significantly greater in plots receiving nitrate additions relative to controls in July 2009. Respiratory rates and CH4 fluxes were not significantly affected. N2O fluxes were significantly higher in dark than in transparent chambers, averaging 108 and 42 μmol N2O m−2 day−1 respectively. After 2 days, when nutrient concentrations returned to background levels, none of the greenhouse gas fluxes differed from controls. In April 2010, N2O and CH4 fluxes were not significantly affected by nitrate, possibly due to higher nitrogen demands by growing S. patens plants, but in June 2010 trends of higher N2O fluxes were again found among nitrate-enriched plots, indicating that responses to nutrient pulses may be strongest during the summer. In terms of carbon equivalents, the highest average N2O and CH4 fluxes observed, exceeded half

  17. Isotope signatures of N2O emitted from vegetable soil: Ammonia oxidation drives N2O production in NH4+-fertilized soil of North China

    NASA Astrophysics Data System (ADS)

    Zhang, Wei; Li, Yuzhong; Xu, Chunying; Li, Qiaozhen; Lin, Wei

    2016-07-01

    Nitrous oxide (N2O) is a potent greenhouse gas. In North China, vegetable fields are amended with high levels of N fertilizer and irrigation water, which causes massive N2O flux. The aim of this study was to determine the contribution of microbial processes to N2O production and characterize isotopic signature effects on N2O source partitioning. We conducted a microcosm study that combined naturally abundant isotopologues and gas inhibitor techniques to analyze N2O flux and its isotopomer signatures [δ15Nbulk, δ18O, and SP (intramolecular 15N site preference)] that emitted from vegetable soil after the addition of NH4+ fertilizers. The results show that ammonia oxidation is the predominant process under high water content (70% water-filled pore space), and nitrifier denitrification contribution increases with increasing N content. δ15Nbulk and δ18O of N2O may not provide information about microbial processes due to great shifts in precursor signatures and atom exchange, especially for soil treated with NH4+ fertilizer. SP and associated two end-member mixing model are useful to distinguish N2O source and contribution. Further work is needed to explore isotopomer signature stability to improve N2O microbial process identification.

  18. Reducing fertilizer-derived N2O emission: Point injection vs. surface application of ammonium-N fertilizer at a loamy sand site

    NASA Astrophysics Data System (ADS)

    Deppe, Marianna; Well, Reinhard; Giesemann, Anette; Kücke, Martin; Flessa, Heinz

    2013-04-01

    N2O emitted from soil originates either from denitrification of nitrate and/or nitrification of ammonium. N fertilization can have an important impact on N2O emission rates. Injection of nitrate-free ammonium-N fertilizer, in Germany also known as CULTAN (Controlled Uptake Long-Term Ammonium Nutrition), results in fertilizer depots with ammonium concentrations of up to 10 mg N g-1 soil-1. High concentrations of ammonium are known to inhibit nitrification. However, it has not yet been clarified how N2O fluxes are affected by CULTAN. In a field experiment, two application methods of nitrogen fertilizer were used at a loamy sand site: Ammonium sulphate was applied either by point injection or by surface application. 15N-ammonium sulphate was used to distinguish between N2O originating from either fertilizer-N or soil-N. Unfertilized plots and plots fertilized with unlabeled ammonium sulphate served as control. N2O emissions were measured using static chambers, nitrate and ammonium concentrations were determined in soil extracts. Stable isotope analysis of 15N in N2O, nitrate and ammonium was used to calculate the contribution of fertilizer N to N2O emissions and the fertilizer turnover in soil. 15N analysis clearly indicated that fertilizer derived N2O fluxes were higher from surface application plots. For the period of the growing season, about 24% of the flux measured in surface application treatment and less than 10% from injection treatment plots originated from the fertilizer. In addition, a lab experiment was conducted to gain insight into processes leading to N2O emission from fertilizer depots. One aim was to examine whether the ratio of N2O to nitrate formation differs depending on the ammonium concentration. Loamy sand soil was incubated in microcosms continuously flushed with air under conditions favouring nitrification. 15N-labeled nitrate was used to differentiate between nitrification and denitrification. Stable isotope analyses of 15N were performed on

  19. Measuring CO 2 and N 2 O Mass Transfer into GAP-1 CO 2 –Capture Solvents at Varied Water Loadings

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    Whyatt, Greg A.; Zwoster, Andy; Zheng, Feng

    This paper investigates the CO 2 and N 2 O absorption behavior in the water-lean gamma amino propyl (GAP)-1/TEG solvent system using a wetted-wall contactor. Testing was performed on a blend of GAP-1 aminosilicone in triethylene glycol at varied water loadings in the solvent. Measurements were made with CO 2 and N 2 O at representative lean (0.04 mol CO 2/mol alkalinity), middle (0.13 mol CO 2 /mol alkalinity) and rich (0.46 mol CO 2 /mol alkalinity) solvent loadings at 0, 5, 10 and 15 wt% water loadings at 40, 60 and 80C° and N 2 O at (0.08-0.09 molmore » CO 2 /mol alkalinity) at 5 wt% water at 40, 60 and 80C°. CO 2 flux was found to be non-linear with respect to log mean pressure driving force (LMPD). Liquid-film mass transfer coefficients (k'g) were calculated by subtracting the gas film resistance (determined from a correlation from literature) from the overall mass transfer measurement. The resulting k'g values for CO 2 and N 2 O in GAP-1/TEG mixtures were found to be higher than that of 5M aqueous monoethanolamine under comparable driving force albeit at higher solvent viscosities. The k'g values for CO 2 were also found to decrease with increasing solvent water content and increase with a decrease in temperature. These observations indicate that mass transfer of CO 2 in GAP-1/TEG is linked to the physical solubility of CO 2 , which is higher in organic solvents compared to water. This paper expands on the understanding of the unique mass transfer behavior and kinetics of CO 2 capture in water-lean solvents.« less

  20. Source portioning of N_{2}O emissions after long term elevation of soil temperature in a permanent grassland soil

    NASA Astrophysics Data System (ADS)

    Jansen-Willems, Anne; Lanigan, Gary; Clough, Timothy; Andresen, Louise; Müller, Christoph

    2016-04-01

    Several methods, such as source portioning, have been used to quantify the contributions of individual N pools to N2O emissions. These methods however, assume the absence of hybrid reactions such as co-denitrification, which were previously identified as important. A straight forward method portioning N2O fluxes into four different production processes, including a hybrid reaction, was therefore developed. This method portioned the N2O fluxes in nitrification, denitrification, oxidation of organic matter and co-denitrification, using data on 45R and 46R of the N2O flux and the 15N content of the NO3- and NH4+ in the soil. This newly developed method was used to analyse the N2O emissions from incubated soil, which was previously subjected to 6 years of elevated soil temperature of +0, +1, +2 or +3 ° C. N2O emissions were measured and analysed at four time points in the six days following, NO315NH4 Gly or 15NO3NH4 Gly, label addition. The oxidation of organic N was found to be the main source of N2O fluxes at all sampling dates, comprising between 63 and 85% of the total N2O flux. The percentage contribution made by organic N to N2O fluxes increased over the sampling period, rising from a minimum of 40% in the control treatment, to virtually 100% across all treatments by Day 6. Compared to the control treatment, denitrification contributed less to N2O from soil subjected to +2 and +3 ° C warming (p <0.0001 and p=0.002, respectively). Co-denitrification only contributed to the N2O flux during the first day after substrate addition. The highest amount of N2O produced via co-denitrification was found under the control treatment. From soil subjected to +2 and +3 ° C treatments, the contribution of co-denitrification was minor. However, these differences in co-denitrification were not significant. This research showed the importance of the oxidation of organic N in N2O emissions. It should therefore not be omitted as a potential source in source portioning. Emissions

  1. Soil-atmospheric exchange of CO2, CH4, and N2O in three subtropical forest ecosystems in southern China

    USGS Publications Warehouse

    Tang, X.; Liu, S.; Zhou, G.; Zhang, Dongxiao; Zhou, C.

    2006-01-01

    The magnitude, temporal, and spatial patterns of soil-atmospheric greenhouse gas (hereafter referred to as GHG) exchanges in forests near the Tropic of Cancer are still highly uncertain. To contribute towards an improvement of actual estimates, soil-atmospheric CO2, CH4, and N2O fluxes were measured in three successional subtropical forests at the Dinghushan Nature Reserve (hereafter referred to as DNR) in southern China. Soils in DNR forests behaved as N2O sources and CH4 sinks. Annual mean CO2, N2O, and CH4 fluxes (mean ?? SD) were 7.7 ?? 4.6MgCO2-Cha-1 yr-1, 3.2 ?? 1.2 kg N2ONha-1 yr-1, and 3.4 ?? 0.9 kgCH4-Cha-1 yr-1, respectively. The climate was warm and wet from April through September 2003 (the hot-humid season) and became cool and dry from October 2003 through March 2004 (the cool-dry season). The seasonality of soil CO2 emission coincided with the seasonal climate pattern, with high CO2 emission rates in the hot-humid season and low rates in the cool-dry season. In contrast, seasonal patterns of CH4 and N2O fluxes were not clear, although higher CH4 uptake rates were often observed in the cool-dry season and higher N2O emission rates were often observed in the hot-humid season. GHG fluxes measured at these three sites showed a clear increasing trend with the progressive succession. If this trend is representative at the regional scale, CO2 and N2O emissions and CH4 uptake in southern China may increase in the future in light of the projected change in forest age structure. Removal of surface litter reduced soil CO2 effluxes by 17-44% in the three forests but had no significant effect on CH4 absorption and N2O emission rates. This suggests that microbial CH4 uptake and N2O production was mainly related to the mineral soil rather than in the surface litter layer. ?? 2006 Blackwell Publishing Ltd.

  2. Constraints on global oceanic emissions of N2O from observations and models

    NASA Astrophysics Data System (ADS)

    Buitenhuis, Erik T.; Suntharalingam, Parvadha; Le Quéré, Corinne

    2018-04-01

    We estimate the global ocean N2O flux to the atmosphere and its confidence interval using a statistical method based on model perturbation simulations and their fit to a database of ΔpN2O (n = 6136). We evaluate two submodels of N2O production. The first submodel splits N2O production into oxic and hypoxic pathways following previous publications. The second submodel explicitly represents the redox transformations of N that lead to N2O production (nitrification and hypoxic denitrification) and N2O consumption (suboxic denitrification), and is presented here for the first time. We perturb both submodels by modifying the key parameters of the N2O cycling pathways (nitrification rates; NH4+ uptake; N2O yields under oxic, hypoxic and suboxic conditions) and determine a set of optimal model parameters by minimisation of a cost function against four databases of N cycle observations. Our estimate of the global oceanic N2O flux resulting from this cost function minimisation derived from observed and model ΔpN2O concentrations is 2.4 ± 0.8 and 2.5 ± 0.8 Tg N yr-1 for the two N2O submodels. These estimates suggest that the currently available observational data of surface ΔpN2O constrain the global N2O flux to a narrower range relative to the large range of results presented in the latest IPCC report.

  3. Effect of Na2O on Crystallisation Behaviour and Heat Transfer of Fluorine-Free Mould Fluxes

    NASA Astrophysics Data System (ADS)

    Yang, Jian; Zhang, Jianqiang; Sasaki, Yasushi; Ostrovski, Oleg; Zhang, Chen; Cai, Dexiang; Kashiwaya, Yoshiaki

    Most of the commercial mould fluxes contain fluorides which bring about serious environmental problems. The major challenge in the application of fluorine-free mould fluxes is to control the heat transfer from the strand to copper mould which is closely related to crystallisation behaviour. In this study, the effects of Na2O on the crystallisation behaviour and heat transfer of CaO-SiO2-Na2O-B2O3-TiO2-Al2O3-MgO-Li2O mould fluxes were investigated using single /double hot thermocouple technique (SHTT/DHTT) and infrared emitter technique (IET), respectively. Continuous cooling transformation (CCT) and time-temperature transformation (TTT) diagrams constructed using SHTT showed that the increase of Na2O concentration led to higher critical cooling rate and shorter incubation time. The crystallisation behaviour in a thermal gradient was examined using DHTT. The heat flux measured by IET showed that the increase of Na2O concentration decreased the heat flux when Na2O was lower than 9 mass% but the further increase of Na2O raised the heat flux. The relationship between flux crystallisation and heat transfer was also discussed.

  4. Tidal and spatial variability of nitrous oxide (N2O) in Sado estuary (Portugal)

    NASA Astrophysics Data System (ADS)

    Gonçalves, Célia; Brogueira, Maria José; Nogueira, Marta

    2015-12-01

    The estimate of the nitrous oxide (N2O) fluxes is fundamental to assess its impact on global warming. The tidal and spatial variability of N2O and the air-sea fluxes in the Sado estuary in July/August 2007 are examined. Measurements of N2O and other relevant environmental parameters (temperature, salinity, dissolved oxygen and dissolved inorganic nitrogen - nitrate plus nitrite and ammonium) were recorded during two diurnal tidal cycles performed in the Bay and Marateca region and along the estuary during ebb, at spring tide. N2O presented tidal and spatial variability and varied spatially from 5.0 nmol L-1 in Marateca region to 12.5 nmol L-1 in Sado river input. Although the Sado river may constitute a considerable N2O source to the estuary, the respective chemical signal discharge was rapidly lost in the main body of the estuary due to the low river flow during the sampling period. N2O varied with tide similarly between 5.2 nmol L-1 (Marateca) and 10.0 nmol L-1 (Sado Bay), with the maximum value reached two hours after flooding period. The influence of N2O enriched upwelled seawater (˜10.0 nmol L-1) was well visible in the estuary mouth and apparently represented an important contribution of N2O in the main body of Sado estuary. Despite the high water column oxygen saturation in most of Sado estuary, nitrification did not seem a relevant process for N2O production, probably as the concentration of the substrate, NH4+, was not adequate for this process to occur. Most of the estuary functioned as a N2O source, and only Marateca zone has acted as N2O sink. The N2O emission from Sado estuary was estimated to be 3.7 Mg N-N2O yr-1 (FC96) (4.4 Mg N-N2O yr-1, FRC01). These results have implications for future sampling and scaling strategies for estimating greenhouse gases (GHGs) fluxes in tidal ecosystems.

  5. [Effects of different fertilization measures on N2O emission in oil sunflower field in irrigation area of upper Yellow River].

    PubMed

    Chen, Zhe; Chen, Yuan-yuan; Gao, Ji; Liu, Ru-liang; Yang, Zheng-li; Zhang, Ai-ping

    2015-01-01

    Agricultural soil has become the largest anthropogenic source of atmospheric nitrous oxide (N20). To estimate the impacts of long-term combined application of organic and inorganic fertilizers on N20 emission in a typical winter wheat-oil sunflower cropping system in the Ningxia irrigation area, we measured N20 fluxes using the static opaque chamber-gas chromatograph method and monitored the seasonal dynamics of related factors. Our results showed that nitrogen addition in the previous crop field significantly stimulated N2O emissions during the following oil-sunflower cultivation, and the mean fluxes of N300-OM, N240-OM1/2, N300 and N240 were (34.16 ± 9.72), (39.69 ±10.70), (27.75 ±9.57) and (26.30 ± 8.52) µg . m-2 . h-1, respectively, which were 4.09, 4.75, 3.32 and 3.15 times of the control groups. The total cumulative N2O emissions of fertilizer treatments in growing season was as high as 796.7 to 1242.5 g . hm-2, which was 2.99 to 4.67 times of the control groups. During the growing season, the rates of N2O emission in each month organic and inorganic fertlizers combined treatments were similar at high levels. N2O emission in chemical fertilizer treatments gradually decreased, and the main period of N2O emission occurred at the beginning of growing season. Taking July for example, N2O emission accounted for 41.3% to 41. 8% of total cumulative amount. The amounts of N20 emission under organic and inorganic fertilizers combined treatments were significantly higher than under chemical fertilizer treatments. The N2O emissions were not significantly different between conventional and optimized applications of nitrogen fertilizer under the same fertilizing method, either between N300-OM and N240-OM1/2, or between N300 and N240. On account of the drought, N2O emission in each treatment was mainly affected by soil moisture. N2O emission had a significant positive correlation with soil ammonium nitrogen content under combined applications of organic and inorganic

  6. Novel microelectrode-based online system for monitoring N2O gas emissions during wastewater treatment.

    PubMed

    Marques, Ricardo; Oehmen, Adrian; Pijuan, Maite

    2014-11-04

    Clark-type nitrous oxide (N2O) microelectrodes are commonly used for measuring dissolved N2O levels, but have not previously been tested for gas-phase applications, where the N2O emitted from wastewater systems can be directly quantified. In this study, N2O microelectrodes were tested and validated for online gas measurements, and assessed with respect to their temperature, gas flow, composition dependence, gas pressure, and humidity. An exponential correlation between temperature and sensor signal was found, whereas gas flow, composition, pressure, and humidity did not have any influence on the signal. Two of the sensors were tested at different N2O concentration ranges (0-422.3, 0-50, 0-10, and 0-2 ppmv N2O) and exhibited a linear response over each range. The N2O emission dynamics from two laboratory scale sequencing batch reactors performing ammonia or nitrite oxidation were also monitored using one of the microsensors and results were compared with two other analytical methods. Results show that N2O emissions were accurately described with these microelectrodes and support their application for assessing gaseous N2O emissions from wastewater treatment systems. Advantages of the sensors as compared to conventional measurement techniques include a wider quantification range of N2O fluxes, and a single measurement system that can assess both liquid and gas-phase N2O dynamics.

  7. In-Situ Denitrification and N2O Emission from Natural and Semi-natural Land Use Types in two UK Catchments

    NASA Astrophysics Data System (ADS)

    Sgouridis, F.; Ullah, S.

    2014-12-01

    Whilst data and understanding of the controls of denitrification process and the subsequent emission of N2O at microbial and plot scale exist, quantification of in situ annual denitrification rates at catchment scales is scarce due to methodological constraints in measuring in situ denitrification in large temporal and spatial scales. In situ denitrification (DNT) was measured monthly (April 2013 - October 2014) in organic (peat bog, heathland, acid grassland), forest (mixed and deciduous), and grassland (improved and semi-improved) land use types in the Ribble-Wyre and Conwy River catchments in the UK. A static chamber technique according to the 15N-Gas Flux method1 was employed for quantifying the fluxes of 15N-N2 and 15N-N2O gases after labelling the soil with 98 at% K15NO3- at tracer level amounts (10% of the ambient nitrate concentration) and sampling the chamber headspace at 0, 1, 2 and 20 hour intervals. The DNT rates ranged between 0 and 2.3 mg N m-2 h-1 and were significantly influenced by land use type (p<0.05). The annual denitrification rate of organic and forest soils (4 kg N ha-1 y-1) was 3 and 6 times less than that of semi-improved (12 kg N ha-1 y-1) and improved (23 kg N ha-1 y-1) grassland soils, respectively. The N2O emission, due to denitrification, followed a similar trend with lower fluxes from organic and higher from improved grassland soils (range: 0 - 0.04 mg N m-2 h-1), whilst the N2O:N2 ratio ranged between 0.2 and 4%. The relative contribution of denitrification to net N2O flux varied temporally and across the different land use types and ranged from 0.2 to 75%. The 15N-Gas Flux method can be successfully applied in a variety of land use types for relatively high temporal and spatial resolution measurement of in situ denitrification and the simultaneous quantification of N2 and N2O fluxes due to denitrification. Therefore the ratio of N2O:N2 and also the source apportionment for N2O can be estimated more accurately. The results suggested

  8. Effect of drainage on CO2, CH4, and N2O fluxes from aquaculture ponds during winter in a subtropical estuary of China.

    PubMed

    Yang, Ping; Lai, Derrick Y F; Huang, Jia F; Tong, Chuan

    2018-03-01

    Aquaculture ponds are dominant features of the landscape in the coastal zone of China. Generally, aquaculture ponds are drained during the non-culture period in winter. However, the effects of such drainage on the production and flux of greenhouse gases (GHGs) from aquaculture ponds are largely unknown. In the present study, field-based research was performed to compare the GHG fluxes between one drained pond (DP, with a water depth of 0.05m) and one undrained pond (UDP, with a water depth of 1.16m) during one winter in the Min River estuary of southeast China. Over the entire study period, the mean CO 2 flux in the DP was (0.75±0.12) mmol/(m 2 ·hr), which was significantly higher than that in the UDP of (-0.49±0.09) mmol/(m 2 ·hr) (p<0.01). This indicates that drainage drastically transforms aquaculture ponds from a net sink to a net source of CO 2 in winter. Mean CH 4 and N 2 O emissions were significantly higher in the DP compared to those in the UDP (CH 4 =(0.66±0.31) vs. (0.07±0.06) mmol/(m 2 ·hr) and N 2 O=(19.54±2.08) vs. (0.01±0.04) µmol/(m 2 ·hr)) (p<0.01), suggesting that drainage would also significantly enhance CH 4 and N 2 O emissions. Changes in environmental variables (including sediment temperature, pH, salinity, redox status, and water depth) contributed significantly to the enhanced GHG emissions following pond drainage. Furthermore, analysis of the sustained-flux global warming and cooling potentials indicated that the combined global warming potentials of the GHG fluxes were significantly higher in the DP than in the UDP (p<0.01), with values of 739.18 and 26.46mgCO 2 -eq/(m 2 ·hr), respectively. Our findings suggested that drainage of aquaculture ponds can increase the emissions of potent GHGs from the coastal zone of China to the atmosphere during winter, further aggravating the problem of global warming. Copyright © 2017. Published by Elsevier B.V.

  9. Slowdown of N2O emissions from China's croplands

    NASA Astrophysics Data System (ADS)

    Zhou, F.; Shang, Z.; Ciais, P.; Piao, S.; Tian, H.; Saikawa, E.; Zaehle, S.; Del Grosso, S. J.; Galloway, J. N.

    2016-12-01

    To feed the increasing population, China has experienced a rapid agricultural development over past decades, accompanied by increased fertilizer consumptions in croplands, but the magnitude, trend, and causes of the associated nitrous oxide (N2O) emissions has remain unclear. The primary sources of this uncertainty are conflicting estimates of fertilizer consumption and emission factors, the latter being uncertain because of very few regional representativeness of the Nrate-flux relationships in China. Here we re-estimate China's N2O emissions from croplands using three different methods: flux upscaling technique, process-based models and atmospheric inversion, and also analyze the corresponding drivers using an attribution approach. The three methods produce similar estimates of N2O emissions in the range of 0.67 ± 0.08 to 0.62± 0.11 Tg nitrogen per year, which is 29% larger than the estimates by the Emission Database for Global Atmospheric Research (EDGAR) that is adopted by Intergovernmental Panel on Climate Change (IPCC) as the emission baseline and twofold larger than the latest Chinese national report submitted to the United Nations Framework Convention on Climate Change, but the revised trend slows down after 2005. Fertilizer N application per area is the dominant factor driving the increase in N2O emissions across most cropping regions from 1990 to 2004, but climate-induced change of emission factors has also controlled N2O flux from 2005 onwards. Our findings suggest that, as precipitation would increase in North China but decline in the South in future, EF will increasingly control China's agri. soil emissions of N2O, unless offset by larger reductions of fertilizer consumptions.

  10. Ability of the current global observing network to constrain N2O sources and sinks

    NASA Astrophysics Data System (ADS)

    Millet, D. B.; Wells, K. C.; Chaliyakunnel, S.; Griffis, T. J.; Henze, D. K.; Bousserez, N.

    2014-12-01

    The global observing network for atmospheric N2O combines flask and in-situ measurements at ground stations with sustained and campaign-based aircraft observations. In this talk we apply a new global model of N2O (based on GEOS-Chem) and its adjoint to assess the strengths and weaknesses of this network for quantifying N2O emissions. We employ an ensemble of pseudo-observation analyses to evaluate the relative constraints provided by ground-based (surface, tall tower) and airborne (HIPPO, CARIBIC) observations, and the extent to which variability (e.g. associated with pulsing or seasonality of emissions) not captured by the a priori inventory can bias the inferred fluxes. We find that the ground-based and HIPPO datasets each provide a stronger constraint on the distribution of global emissions than does the CARIBIC dataset on its own. Given appropriate initial conditions, we find that our inferred surface fluxes are insensitive to model errors in the stratospheric loss rate of N2O over the timescale of our analysis (2 years); however, the same is not necessarily true for model errors in stratosphere-troposphere exchange. Finally, we examine the a posteriori error reduction distribution to identify priority locations for future N2O measurements.

  11. Sun photometer and lidar measurements of the plume from the Hawaii Kilauea Volcano Pu'u O'o vent: Aerosol flux and SO2 lifetime

    USGS Publications Warehouse

    Porter, J.N.; Horton, K.A.; Mouginis-Mark, P. J.; Lienert, B.; Sharma, S.K.; Lau, E.; Sutton, A.J.; Elias, T.; Oppenheimer, C.

    2002-01-01

    Aerosol optical depths and lidar measurements were obtained under the plume of Hawaii Kilauea Volcano on August 17, 2001, ???9 km downwind from the erupting Pu'u O'o vent. Measured aerosol optical depths (at 500 nm) were between 0.2-0.4. Aerosol size distributions inverted from the spectral sun photometer measurements suggest the volcanic aerosol is present in the accumulation mode (0.1-0.5 micron diameter), which is consistent with past in situ optical counter measurements. The aerosol dry mass flux rate was calculated to be 53 Mg d-1. The estimated SO2 emission rate during the aerosol measurements was ???1450 Mg d-1. Assuming the sulfur emissions at Pu'u O'o vent are mainly SO2 (not aerosol), this corresponds to a SO2 half-life of 6.0 hours in the atmosphere.

  12. Eddy-correlation measurements of fluxes of CO 2 and H 2O above a spruce stand

    NASA Astrophysics Data System (ADS)

    Ibrom, A.; Schütz, C.; Tworek, T.; Morgenstern, K.; Oltchev, A.; Falk, M.; Constantin, J.; Gravenhorst, G.

    1996-12-01

    Atmospheric fluxes of CO 2 and H 2O above a mature spruce stand ( Picea abies (L.) Karst.) have been investigated using the eddy- correlation technique. A closed path sensor adapted to the special requirements of long-term studies has been developed and tested. Field measurements have been performed since April 1995. Estimates of fetch showed a very narrow source area dimension under instable stratification (≤ 200 m). Fetch requirements at night are not met in some directions. Energy balance closure was influenced systematically by the wind direction indicating a substantial attenuation of the vertical wind motion by the tower (up to 40 %). Even for optimal flow directions, energy balance closure was about 88%. Intercomparison of the used ultra sonic anemometer (USAT-3) with a GILL - anemometer showed systematically lower values of vertical wind speed fluctuations (13 %). Average CO 2-fluxes ranged between -13 at noon to 3 μ mol m-2, s-1 at night in summer. In November and December the stand released CO 2 on a daily basis. A preliminary estimate of the cumulative net carbon balance over the observed period of 9 months is 4-5 t, Cha-1.

  13. Nitrous oxide flux following tropical land clearing

    NASA Technical Reports Server (NTRS)

    Luizao, Flavio; Luizao, Regina; Matson, Pamela; Livingston, Gerald; Vitousek, Peter

    1989-01-01

    The importance of seasonal cycles of N2O flux from tropical ecosystems and the possibility that tropical deforestation could contribute to the ongoing global increase in N2O concentrations were assessed by measuring N2O flux from forest, cleared land, and pasture over an annual cycle in the central Amazon. A pasture that had been converted from tropical forest had threefold greater annual N2O flux than a paired forest site; similar results were obtained in spot measurements in other pastures. If these results are general, such tropical pastures represent a globally significant source of increased N2O.

  14. Nitrous oxide flux following tropical land clearing

    NASA Astrophysics Data System (ADS)

    LuizãO, FláVio; Matson, Pamela; Livingston, Gerald; LuizãO, Regina; Vitousek, Peter

    1989-09-01

    The importance of seasonal cycles of N2O flux from tropical ecosystems and the possibility that tropical deforestation could contribute to the ongoing global increase in N2O concentrations were assessed by measuring N2O flux from forest, cleared land, and pasture over an annual cycle in the central Amazon. A pasture that had been converted from tropical forest had threefold greater annual N2O flux than a paired forest site; similar results were obtained in spot measurements in other pastures. If these results are general, such tropical pastures represent a globally significant source of increased N2O.

  15. Nitrous Oxide (N2O) Emissions from California based on 2010 CalNex Airborne Measurements

    NASA Astrophysics Data System (ADS)

    Xiang, B.; Miller, S.; Kort, E. A.; Santoni, G. W.; Daube, B.; Commane, R.; Angevine, W. M.; Ryerson, T. B.; Trainer, M.; Andrews, A. E.; Nehrkorn, T.; Tian, H.; Wofsy, S. C.

    2012-12-01

    Nitrous oxide (N2O) is an important gas for climate and for stratospheric chemistry, with an atmospheric lifetime exceeding 100 years. Global concentrations have increased steadily since the 18th century, apparently due to human-associated emissions, principally from application of nitrogen fertilizers. However, quantitative studies of agricultural emissions at large spatial scales are lacking, inhibited by the difficulty of measuring small enhancements of atmospheric concentrations. Here we derive regional emission rates for N2O in the Central Valley of California, based on analysis of in-situ airborne atmospheric observations collected using a quantum cascade laser spectrometer. The data were obtained on board the NOAA P-3 research aircraft during the CalNex (California Research at the Nexus of Air Quality and Climate Change) program in May and June, 2010. We coupled WRF (Weather Research and Forecasting) model to STILT (Stochastic Time-Inverted Lagrangian Transport) to link our in-situ observations to surface emissions, and then used a variety of statistical methods to identify source areas and to extract optimized emission rates from the inversion. Our results support the view that fertilizer application is the largest source of N2O in the Central Valley. But the spatial distribution of derived surface emissions, based on California land use and activity maps, was very different than indicated in the leading emissions inventory (EDGAR 4.0), and our estimated total emission flux of N2O for California during the study period was 3 - 4 times larger than EDGAR and other inventories.

  16. Technical Note: Simultaneous measurement of sedimentary N2 and N2O production and a modified 15N isotope pairing technique

    NASA Astrophysics Data System (ADS)

    Hsu, T.-C.; Kao, S.-J.

    2013-12-01

    Dinitrogen (N2) and/or nitrous oxide (N2O) are produced through denitrification, anaerobic ammonium oxidation (anammox) or nitrification in sediments, of which entangled processes complicate the absolute rate estimations of gaseous nitrogen production from individual pathways. The classical isotope pairing technique (IPT), the most common 15N nitrate enrichment method to quantify denitrification, has recently been modified by different researchers to (1) discriminate between the N2 produced by denitrification and anammox or to (2) provide a more accurate denitrification rate under considering production of both N2O and N2. In case 1, the revised IPT focused on N2 production being suitable for the environments of a low N2O-to-N2 production ratio, while in case 2, anammox was neglected. This paper develops a modified method to refine previous versions of IPT. Cryogenic traps were installed to separately preconcentrate N2 and N2O, thus allowing for subsequent measurement of the two gases generated in one sample vial. The precision is better than 2% for N2 (m/z 28, m/z 29 and m/z 30), and 1.5% for N2O (m/z 44, m/z 45 and m/z 46). Based on the six m/z peaks of the two gases, the 15N nitrate traceable processes including N2 and N2O from denitrification and N2 from anammox were estimated. Meanwhile, N2O produced by nitrification was estimated via the production rate of unlabeled 44N2O. To validate the applicability of our modified method, incubation experiments were conducted using sediment cores taken from the Danshuei Estuary in Taiwan. Rates of the aforementioned nitrogen removal processes were successfully determined. Moreover, N2O yield was as high as 66%, which would significantly bias previous IPT approaches if N2O was not considered. Our modified method not only complements previous versions of IPT but also provides more comprehensive information to advance our understanding of nitrogen dynamics of the water-sediment interface.

  17. Stable Isotopes of N2O in a Large Canadian River Impacted by Agricultural and Urban Land Use

    NASA Astrophysics Data System (ADS)

    Thuss, S. J.; Rosamond, M. S.; Schiff, S.; Venkiteswaran, J. J.; Elgood, R. J.

    2009-05-01

    N2O is a potent greenhouse gas. Although denitrification is an important process in the global N cycle, N2O flux measurements from rivers worldwide are scarce. The two main processes producing N2O in rivers -- nitrification and denitrification -- result in N2O that is widely separated in isotopic signature. However, studies on the stable isotopes of N2O in rivers are almost non-existent. Here, we report the N2O fluxes and isotopic signatures in the Grand River, a large, heavily impacted river in southern Ontario. Land use in the basin is predominately agricultural and the river receives effluent from 26 wastewater treatment plants (WWTPs). River samples were collected over a 28 hour period to capture diel variation, along the entire length of the river to capture changing land use and throughout the year to capture the seasonal variability. A dynamic model was used to correct the measured N2O values for the effects of atmospheric exchange. Isotopic analysis of both the NH4+ and the NO3- end members in the WWTP effluent and in the river allowed the determination of N2O production pathways. N2O is produced along the entire length of the river but N2O from denitrification increases dramatically in the river below WWTPs at night when dissolved oxygen is low and nitrification of NH4+ decreases.

  18. The vibration-rotation-tunneling levels of N2-H2O and N2-D2O.

    PubMed

    Wang, Xiao-Gang; Carrington, Tucker

    2015-07-14

    In this paper, we report vibration-rotation-tunneling levels of the van der Waals clusters N2-H2O and N2-D2O computed from an ab initio potential energy surface. The only dynamical approximation is that the monomers are rigid. We use a symmetry adapted Lanczos algorithm and an uncoupled product basis set. The pattern of the cluster's levels is complicated by splittings caused by H-H exchange tunneling (larger splitting) and N-N exchange tunneling (smaller splitting). An interesting result that emerges from our calculation is that whereas in N2-H2O, the symmetric H-H tunnelling state is below the anti-symmetric H-H tunnelling state for both K = 0 and K = 1, the order is reversed in N2-D2O for K = 1. The only experimental splitting measurements are the D-D exchange tunneling splittings reported by Zhu et al. [J. Chem. Phys. 139, 214309 (2013)] for N2-D2O in the v2 = 1 region of D2O. Due to the inverted order of the split levels, they measure the sum of the K = 0 and K = 1 tunneling splittings, which is in excellent agreement with our calculated result. Other splittings we predict, in particular those of N2-H2O, may guide future experiments.

  19. The vibration-rotation-tunneling levels of N2-H2O and N2-D2O

    NASA Astrophysics Data System (ADS)

    Wang, Xiao-Gang; Carrington, Tucker

    2015-07-01

    In this paper, we report vibration-rotation-tunneling levels of the van der Waals clusters N2-H2O and N2-D2O computed from an ab initio potential energy surface. The only dynamical approximation is that the monomers are rigid. We use a symmetry adapted Lanczos algorithm and an uncoupled product basis set. The pattern of the cluster's levels is complicated by splittings caused by H-H exchange tunneling (larger splitting) and N-N exchange tunneling (smaller splitting). An interesting result that emerges from our calculation is that whereas in N2-H2O, the symmetric H-H tunnelling state is below the anti-symmetric H-H tunnelling state for both K = 0 and K = 1, the order is reversed in N2-D2O for K = 1. The only experimental splitting measurements are the D-D exchange tunneling splittings reported by Zhu et al. [J. Chem. Phys. 139, 214309 (2013)] for N2-D2O in the v2 = 1 region of D2O. Due to the inverted order of the split levels, they measure the sum of the K = 0 and K = 1 tunneling splittings, which is in excellent agreement with our calculated result. Other splittings we predict, in particular those of N2-H2O, may guide future experiments.

  20. Measuring and modeling the effects of drainage water management on soil greenhouse gas fluxes from corn and soybean fields.

    PubMed

    Nangia, V; Sunohara, M D; Topp, E; Gregorich, E G; Drury, C F; Gottschall, N; Lapen, D R

    2013-11-15

    Controlled tile drainage can boost crop yields and improve water quality, but it also has the potential to increase GHG emissions. This study compared in-situ chamber-based measures of soil CH4, N2O, and CO2 fluxes for silt loam soil under corn and soybean cropping with conventional tile drainage (UTD) and controlled tile drainage (CTD). A semi-empirical model (NEMIS-NOE) was also used to predict soil N2O fluxes from soils using observed soil data. Observed N2O and CH4 fluxes between UTD and CTD fields during the farming season were not significantly different at 0.05 level. Soils were primarily a sink for CH4 but in some cases a source (sources were associated exclusively with CTD). The average N2O fluxes measured ranged between 0.003 and 0.028 kg N ha(-1) day(-1). There were some significantly higher (p ≤ 0.05) CO2 fluxes associated with CTD relative to UTD during some years of study. Correlation analyses indicated that the shallower the water table, the greater the CO2 fluxes. Higher corn plant C for CTD tended to offset estimated higher CTD CO2 C losses via soil respiration by ∼100-300 kg C ha(-1). There were good fits between observed and predicted (NEMIS-NOE) N2O fluxes for corn (R(2) = 0.70) and soybean (R(2) = 0.53). Predicted N2O fluxes were higher for CTD for approximately 70% of the paired-field study periods suggesting that soil physical factors, such as water-filled pore space, imposed by CTD have potentially strong impacts on net N fluxes. Model predictions of daily cumulative N2O fluxes for the agronomically-active study period for corn-CTD and corn-UTD, as a percentage of total N fertilizer applied, were 3.1% and 2.6%, respectively. For predicted N2O fluxes on basis of yield units, indices were 0.0005 and 0.0004 (kg N kg(-1) crop grain yield) for CTD and UTD corn fields, respectively, and 0.0011 and 0.0005 for CTD and UTD soybean fields, respectively. Crown Copyright © 2013. Published by Elsevier Ltd. All rights reserved.

  1. Emissions of N2O and NO from fertilized fields: Summary of available measurement data

    NASA Astrophysics Data System (ADS)

    Bouwman, A. F.; Boumans, L. J. M.; Batjes, N. H.

    2002-12-01

    Information from 846 N2O emission measurements in agricultural fields and 99 measurements for NO emissions was summarized to assess the influence of various factors regulating emissions from mineral soils. The data indicate that there is a strong increase of both N2O and NO emissions accompanying N application rates, and soils with high organic-C content show higher emissions than less fertile soils. A fine soil texture, restricted drainage, and neutral to slightly acidic conditions favor N2O emission, while (though not significant) a good soil drainage, coarse texture, and neutral soil reaction favor NO emission. Fertilizer type and crop type are important factors for N2O but not for NO, while the fertilizer application mode has a significant influence on NO only. Regarding the measurements, longer measurement periods yield more of the fertilization effect on N2O and NO emissions, and intensive measurements (≥1 per day) yield lower emissions than less intensive measurements (2-3 per week). The available data can be used to develop simple models based on the major regulating factors which describe the spatial variability of emissions of N2O and NO with less uncertainty than emission factor approaches based on country N inputs, as currently used in national emission inventories.

  2. Wetting-induced pulses produced unexpectedly high emissions of N2O and NOx in a desert ecosystem

    NASA Astrophysics Data System (ADS)

    Eberwein, J. R.; Carey, C.; Aronson, E. L.; Jenerette, D.

    2015-12-01

    Approximately one third of Earth's land surface is subjected to arid conditions, and aridland soils have the potential for significant feedbacks to global climate change drivers, such as anthropogenic nitrogen deposition. This study examined wetting-induced pulses of N2O and NOx along a nitrogen deposition gradient in the Colorado Desert of southern California. Measurements were made before and following water (to simulate a 2 cm rain event) and nitrogen plus water additions (30 kg NH4NO3 ha-1) at 15 minutes, 12 hours and 24 hours post-wetting. We found nitrogenous fluxes that were substantially higher than expected. N2O fluxes, in particular were remarkably high reaching up to 200 ng N2O-N m-2 s-1, similar to agriculture levels and in the range of peat bog emissions. There was a clear transition between N2O emissions, which peaked 15 minutes after wetting, and NOx emissions, which peaked at the 12 hour timepoint. NOx emissions were also considerable, reaching as high as 350 ng NOx-N m-2 s-1. Both N2O and NOx fluxes responded strongly to water additions, demonstrating a clear wetting-induced pulse response. While N2O was not affected by nitrogen additions, NOx fluxes demonstrated a significant increase with nitrogen plus water over water alone (p=0.016). These results suggest that gaseous nitrogen export, particularly N2O emissions, is a greater form of nitrogen loss in arid systems than is currently assumed. This potential for high nitrogen emissions and the capacity for anthropogenic nitrogen deposition to increase these emissions present serious implications for local air quality and significant soil feedbacks to climate change.

  3. N(2)O emissions and source processes in snow-covered soils in the Swiss Alps.

    PubMed

    Mohn, Joachim; Steinlin, Christine; Merbold, Lutz; Emmenegger, Lukas; Hagedorn, Frank

    2013-01-01

    Nitrous oxide (N2O) emissions from snow-covered soils represent a significant fraction of the annual flux from alpine, subalpine or cold-temperate regions. In winter 2010-2011, we investigated the temporal variability of N2O emissions and source processes from a subalpine valley in the Swiss Alps. The study included regular measurements of N2O snow profiles at a fixed location and an intensive sampling campaign along a transversal cut through the valley with grassland at the bottom and coniferous forest at the slopes. During the intensive campaign, recently developed laser spectroscopy was employed for high-precision N2O isotopomer analysis. Maximum N2O fluxes (0.77±0.64 nmol m(-2) h(-1)) were found for periods with elevated air temperature and, in contrast to our expectations, were higher from forest than from grassland in mid-February. At maximum snow height (63 cm) the main N2O source processes were heterotrophic denitrification and nitrifier denitrification. The reduction of N2O by heterotrophic denitrifiers was much more pronounced for the grassland compared with the forest soil, as indicated by the (15)N site preferences of 16.4±11.5 ‰ (grassland) and-1.6±2.1 ‰ (forest). This illustrates the potential of laser spectroscopic N2O isotopomer analysis for the identification of source processes even at low emission rates in nutrient poor ecosystems.

  4. Laboratory-scale measurements of N2O and CH4 emissions from hybrid poplars (Populus deltoides x Populus nigra).

    PubMed

    McBain, M C; Warland, J S; McBride, R A; Wagner-Riddle, C

    2004-12-01

    The purpose of this study was to determine whether or not young hybrid poplar (Populus deltoides x Populus nigra) could transport landfill biogas internally from the root zone to the atmosphere, thereby acting as conduits for landfill gas release. Fluxes of methane (CH4) and nitrous oxide (N2O) from the seedlings to the atmosphere were measured under controlled conditions using dynamic flux chambers and a tunable diode laser trace gas analyser (TDLTGA). Nitrous oxide was emitted from the seedlings, but only when extremely high soil N2O concentrations were applied to the root zone. In contrast, no detectable emissions of CH4 were measured in a similar experimental trial. Visible plant morphological responses, characteristic of flood-tolerant trees attempting to cope with the negative effects of soil hypoxia, were observed during the CH4 experiments. Leaf chlorosis, leaf abscission and adventitious roots were all visible plant responses. In addition, seedling survival was observed to be highest in the biogas 'hot spot' areas of a local municipal solid waste landfill involved in this study. Based on the available literature, these observations suggest that CH4 can be transported internally by Populus deltoides x Populus nigra seedlings in trace amounts, although future research is required to fully test this hypothesis.

  5. Intercomparison of fast response commercial gas analysers for nitrous oxide flux measurements under field conditions

    NASA Astrophysics Data System (ADS)

    Rannik, Ü.; Haapanala, S.; Shurpali, N. J.; Mammarella, I.; Lind, S.; Hyvönen, N.; Peltola, O.; Zahniser, M.; Martikainen, P. J.; Vesala, T.

    2014-08-01

    Four gas analysers capable of measuring nitrous oxide (N2O) concentration at a response time necessary for eddy covariance flux measurements were operated from spring till winter 2011 over a field cultivated with reed canary grass (RCG, Phalaris arundinaceae, L.), a perennial bioenergy crop in Eastern Finland. The instruments were TGA100A (Campbell Scientific Inc.), CW-TILDAS-CS (Aerodyne Research Inc.), N2O/CO-23d (Los Gatos Research Inc.) and QC-TILDAS-76-CS (Aerodyne Research Inc.). The period with high emission, lasting for about two weeks after fertilization in late May, was characterised by an up to two orders of magnitude higher emission, whereas during the rest of the campaign the N2O fluxes were small, from 0.1 to 1 nmol m-2 s-1. Two instruments, CW-TILDAS-CS and N2O/CO-23d, determined the N2O exchange with minor systematic difference throughout the campaign, when operated simultaneously. TGA100A produced cumulatively highest N2O estimates (with 29% higher value during the period when all instruments were operational). QC-TILDAS-76-CS obtained 36% lower fluxes than CW-TILDAS-CS during the first period, including the emission episode, whereas the correspondence with other instruments during the rest of the campaign was good. The reason for these episodic higher and lower estimates by the two instruments is not currently known, suggesting further need for detailed evaluation of instrument performance under field conditions with emphasis on stability, calibration and, in particular, simultaneous accurate determination of water vapour concentration due to its large impact on small N2O fluxes through spectroscopic and dilution corrections. The instrument CW-TILDAS-CS was characterised by the lowest noise level (std around 0.12 ppb at 10 Hz sampling rate), as compared to N2O/CO-23d and QC-TILDAS-76-CS (around 0.50 ppb) and TGA100A (around 2 ppb). Both instruments based on Continuous-Wave Quantum Cascade Lasers, CW-TILDAS-CS and N2O/CO-23d, were able to determine

  6. O2 absorption cross sections /187-225 nm/ from stratospheric solar flux measurements

    NASA Technical Reports Server (NTRS)

    Herman, J. R.; Mentall, J. E.

    1982-01-01

    The absorption cross sections of molecular oxygen are calculated in the wavelength range from 187 to 230 nm from solar flux measurements obtained within the stratosphere. Within the Herzberg continuum wavelength region the molecular oxygen cross sections are found to be about 30% smaller than the laboratory results of Shardanand and Rao (1977) from 200 to 210 nm and about 50% smaller than those of Hasson and Nicholls (1971). At wavelengths longer than 210 nm the cross sections agree with those of Shardanand and Rao. The effective absorption cross sections of O2 in the Schumann-Runge band region from 187 to 200 nm are calculated and compared to the empirical fit given by Allen and Frederick (1982). The calculated cross sections indicate that the transmissivity of the atmosphere may be underestimated by the use of the Allen and Frederic cross sections between 195 and 200 nm. The ozone column content between 30 and 40 km and the relative ozone cross sections are determined from the same solar flux data set.

  7. Role of plant-generated water vapor and VOC fluxes in shoot chamber measurements of O3 and NOx

    NASA Astrophysics Data System (ADS)

    Joensuu, J.; Altimir, N.; Raivonen, M.; Kolari, P.; Keronen, P.; Vesala, T.; Bäck, J.; Hari, P.; Järvinen, E.; Nikinmaa, E.

    2012-04-01

    One of the processes underlying the atmospheric balance of O3 and NOx is their interaction with vegetation. Both are removed, absorbed, and NOx potentially also emitted by foliage. Uncertainties remain on relevant factors controlling O3 and NOx interactions with foliage as well as on including them in large-scale models. One reason for the uncertainty is that chamber measurements of O3 and NOx fluxes are complicated. These reactive gases are adsorbed and desorbed on the chamber walls, depending on the conditions (i.e. humidity). These artefact gas fluxes (chamber blank) must also be quantified and taken into account in the data analysis. Their importance increases when measuring in clean air, where the fluxes are generally small. At near-zero concentrations, the fluxes may not pass the detection limit of the instrumentation, which usually means it is not possible to separate the plant-related fluxes from the chamber blank. The long-term field measurements at the SMEAR II station in Hyytiälä, Southern Finland, have provided valuable insights into O3 and NOx exchange (i.e. Raivonen & al. 2009, Altimir & al. 2006). This project builds up on the expertise and conclusions from these works. The aim of this study was to improve the reliability of the measuring system by checking the role of potential measuring artefact(s). A live shoot, enclosed in a chamber, creates a water vapor in the chamber flux by transpiring. There are also biogenic VOC emissions from the shoot. In principle, these may affect the reactions of O3 and possibly NOx in the chamber. The potential interference of these fluxes created naturally during chamber closure is a main concern. Their effect on the O3 and NOx flux measurements has been tested with field calibrations in 2010-2011. In these calibrations, a controlled water vapor /VOC flux was fed into an empty shoot measurement chamber, and the H2O, CO2, O3 and NOx fluxes created in the chamber were measured. The created water vapor flux pattern

  8. N2O emission characteristics and its affecting factors in rain-fed potato fields in Wuchuan County, China

    NASA Astrophysics Data System (ADS)

    Wang, Liwei; Wang, Cheng; Pan, Zhihua; Xu, Hui; Gao, Lin; Zhao, Peiyi; Dong, Zhiqiang; Zhang, Jingting; Cui, Guohui; Wang, Sen; Han, Guolin; Zhao, hui

    2017-05-01

    Representing an important greenhouse gas, nitrous oxide (N2O) emission from cultivated land is a hot topic in current climate change research. This study examined the influences of nitrogen fertilisation, temperature and soil moisture on the ammonia monooxygenase subunit A ( amoA) gene copy numbers and N2O emission characteristics. The experimental observation of N2O fluxes was based on the static chamber-gas chromatographic method. The ammonia-oxidising bacteria (AOB) and ammonia-oxidising archaea (AOA) gene copy numbers in different periods were measured by real-time polymerase chain reaction (PCR). The results indicated that rain-fed potato field was a N2O source, and the average annual N2O emission was approximately 0.46 ± 0.06 kgN2O-N/ha/year. N2O emissions increased significantly with increase in fertilisation, temperatures below 19.6 °C and soil volumetric water content under 15%. Crop rotation appreciably decreases N2O emissions by 34.4 to 52.4% compared to continuous cropping in rain-fed potato fields. The significant correlation between N2O fluxes and AOB copy numbers implied that N2O emissions were primarily controlled by AOB in rain-fed potato fields. The research has important theoretical and practical value for understanding N2O emissions from rain-fed dry farmland fields.

  9. N2O emission characteristics and its affecting factors in rain-fed potato fields in Wuchuan County, China.

    PubMed

    Wang, Liwei; Wang, Cheng; Pan, Zhihua; Xu, Hui; Gao, Lin; Zhao, Peiyi; Dong, Zhiqiang; Zhang, Jingting; Cui, Guohui; Wang, Sen; Han, Guolin; Zhao, Hui

    2017-05-01

    Representing an important greenhouse gas, nitrous oxide (N 2 O) emission from cultivated land is a hot topic in current climate change research. This study examined the influences of nitrogen fertilisation, temperature and soil moisture on the ammonia monooxygenase subunit A (amoA) gene copy numbers and N 2 O emission characteristics. The experimental observation of N 2 O fluxes was based on the static chamber-gas chromatographic method. The ammonia-oxidising bacteria (AOB) and ammonia-oxidising archaea (AOA) gene copy numbers in different periods were measured by real-time polymerase chain reaction (PCR). The results indicated that rain-fed potato field was a N 2 O source, and the average annual N 2 O emission was approximately 0.46 ± 0.06 kgN 2 O-N/ha/year. N 2 O emissions increased significantly with increase in fertilisation, temperatures below 19.6 °C and soil volumetric water content under 15%. Crop rotation appreciably decreases N 2 O emissions by 34.4 to 52.4% compared to continuous cropping in rain-fed potato fields. The significant correlation between N 2 O fluxes and AOB copy numbers implied that N 2 O emissions were primarily controlled by AOB in rain-fed potato fields. The research has important theoretical and practical value for understanding N 2 O emissions from rain-fed dry farmland fields.

  10. The partitioning of N2O emissions between denitrification and other sources in natural and semi-natural land use types in the UK.

    NASA Astrophysics Data System (ADS)

    Sgouridis, Fotis; Ullah, Sami

    2017-04-01

    Natural and semi-natural terrestrial ecosystems (unmanaged peatlands and forests, extensive and intensive grasslands) have been under-represented in the UK greenhouse gas (GHG) inventory, thus increasing the uncertainty of annual GHG emission estimates. This uncertainty is further exacerbated by the high spatio-temporal variability of the processes responsible for nitrous oxide (N2O) emission. The partitioning of N2O emission to its different sources can further improve our understanding of the controls on the different microbial processes responsible for N2O production and consumption and ultimately inform GHG mitigation strategies. We have measured in situ N2O fluxes from natural and semi-natural ecosystems in two replicated UK catchments monthly between April 2013 and October 2014. An adapted 15N-Gas Flux method1 for low level additions of 15N tracer (0.03 - 0.5 kg 15N ha-1) appropriate for natural (unfertilised) ecosystems was used to quantify denitrification2 and elucidate its relative contribution to net N2O production. Total N2O fluxes were 40 times higher in the intensive grasslands than in the peatlands and ranged between 0.05 and 1.98 kg N ha-1 y-1. The mean contribution of denitrification to the total N2O flux (DN2O/TN2O) ranged between 9 and 59 % and was lowest in a well-drained forest and highest in a poorly-drained forest soil, while in peatlands and grassland soils it was 48% and 41% on average, respectively. Soil moisture was shown as the key environmental driver regulating the partitioning of N2O between denitrification and other sources (r2=0.46) across land use types. Total N2O fluxes across land use types were explained by a simple regression model (r2=0.83) including parameters such as total dissolved nitrogen, organic carbon availability and volumetric water content. Nitrous oxide emission factors (EFs) calculated as a fraction of mineral N inputs averaged at 0.4 and 0.9% for the semi-improved and improved grasslands, respectively. Using

  11. O2 Herzberg State Reaction with N2: A Possible Source of Stratospheric N2O

    NASA Technical Reports Server (NTRS)

    Slanger, Tom G.; Copeland, Richard A.

    1997-01-01

    The goal of this one-year investigation was to determine whether N2O is formed in atmospherically significant quantities by the reaction of vibrationally excited levels of the O2((A3 Sigma(sub u)(sup +)) state with nitrogen. O2(A3 Sigma(sub u)(sup +)) is made throughout the upper stratosphere in considerable amounts by solar photoabsorption, and only a very small reactive yield is necessary for this mechanism to be a major N2O source. By long-term 245-252 nm irradiation of O2/N2 mixtures on- and off-resonance with absorption lines in the O2(A3 Sigma(sub u)(sup +) - X3 Sigma(sub g)(sup -)) transition, followed by N2O analysis by frequency-modulated diode laser absorption spectroscopy, we determined an upper limit for the N2O yield of the candidate reaction. This limit, 3 x 10(exp -5), eliminates O2(A3 Sigma(sub u)(sup +)) + N2 as a significant channel for the generation of stratospheric N2O. In further measurements, we established that N2O is stable under our photolysis conditions, showing that the small amounts of ozone generated from the reaction of O2(A) and O2 do not indirectly lead to destruction of N2O.

  12. Short-term drought response of N 2O and CO 2 emissions from mesic agricultural soils in the US Midwest

    DOE PAGES

    Gelfand, Ilya; Cui, Mengdi; Tang, Jianwu; ...

    2015-07-17

    Climate change is causing the intensification of both rainfall and droughts in temperate climatic zones, which will affect soil drying and rewetting cycles and associated processes such as soil greenhouse gas (GHG) fluxes. Here, we investigated the effect of soil rewetting following a prolonged natural drought on soil emissions of nitrous oxide (N 2O) and carbon dioxide (CO 2) in an agricultural field recently converted from 22 years in the USDA Conservation Reserve Program (CRP). We compared responses to those in a similarly managed field with no CRP history and to a CRP reference field. We additionally compared soil GHGmore » emissions measured by static flux chambers with off-site laboratory analysis versus in situ analysis using a portable quantum cascade laser and infrared gas analyzer. Under growing season drought conditions, average soil N 2O fluxes ranged between 0.2 and 0.8 μg N m -2 min -1 and were higher in former CRP soils and unaffected by nitrogen (N) fertilization. After 18 days of drought, a 50 mm rewetting event increased N 2O fluxes by 34 and 24 fold respectively in the former CRP and non-CRP soils. Average soil CO 2 emissions during drought ranged from 1.1 to 3.1 mg C m -2 min -1 for the three systems. CO 2 emissions increased ~2 fold after the rewetting and were higher from soils with higher C contents. Observations are consistent with the hypothesis that during drought soil N 2O emissions are controlled by available C and following rewetting additionally influenced by N availability, whereas soil CO 2 emissions are independent of short-term N availability. Finally, soil GHG emissions estimated by off-site and in situ methods were statistically identical.« less

  13. Selective Encaging of N2O in N2O-N2 Binary Gas Hydrates via Hydrate-Based Gas Separation.

    PubMed

    Yang, Youjeong; Shin, Donghoon; Choi, Seunghyun; Woo, Yesol; Lee, Jong-Won; Kim, Dongseon; Shin, Hee-Young; Cha, Minjun; Yoon, Ji-Ho

    2017-03-21

    The crystal structure and guest inclusion behaviors of nitrous oxide-nitrogen (N 2 O-N 2 ) binary gas hydrates formed from N 2 O/N 2 gas mixtures are determined through spectroscopic analysis. Powder X-ray diffraction results indicate that the crystal structure of all the N 2 O-N 2 binary gas hydrates is identified as the structure I (sI) hydrate. Raman spectra for the N 2 O-N 2 binary gas hydrate formed from N 2 O/N 2 (80/20, 60/40, 40/60 mol %) gas mixtures reveal that N 2 O molecules occupy both large and small cages of the sI hydrate. In contrast, there is a single Raman band of N 2 O molecules for the N 2 O-N 2 binary gas hydrate formed from the N 2 O/N 2 (20/80 mol %) gas mixture, indicating that N 2 O molecules are trapped in only large cages of the sI hydrate. From temperature-dependent Raman spectra and the Predictive Soave-Redlich-Kwong (PSRK) model calculation, we confirm the self-preservation of N 2 O-N 2 binary gas hydrates in the temperature range of 210-270 K. Both the experimental measurements and the PSRK model calculations demonstrate the preferential occupation of N 2 O molecules rather than N 2 molecules in the hydrate cages, leading to a possible process for separating N 2 O from gas mixtures via hydrate formation. The phase equilibrium conditions, pseudo-pressure-composition (P-x) diagram, and gas storage capacity of N 2 O-N 2 binary gas hydrates are discussed in detail.

  14. Using satellite measurements of N2O to remove dynamical variability from HCl measurements

    NASA Astrophysics Data System (ADS)

    Stolarski, Richard S.; Douglass, Anne R.; Strahan, Susan E.

    2018-04-01

    Column HCl measurements show deviations from the expected slow decline following the regulation of chlorine-containing compounds by the Montreal Protocol. We use the simultaneous measurements of N2O and HCl by the Microwave Limb Sounder (MLS) instrument on the Aura satellite to examine this problem. We find that the use of N2O measurements at a specific altitude to represent the impact of dynamical variability on HCl results in a derived linear trend in HCl that is negative (ranging from -2.5 to 5.3 % decade-1) at all altitudes between 68 and 10 hPa. These trends are at or near 2σ statistical significance at all pressure levels between 68 and 10 hPa. This shows that analysis of simultaneous measurements of several constituents is a useful approach to identify small trends from data records that are strongly influenced by dynamical interannual variability.

  15. The fluxes of H2O2 and O2 can be used to evaluate seed germination and vigor of Caragana korshinskii.

    PubMed

    Li, Jiaguo; Wang, Yu; Pritchard, Hugh W; Wang, Xiaofeng

    2014-06-01

    Seed deterioration is detrimental to plant germplasm conservation, and predicting seed germination and vigor with reliability and sensitivity means is urgently needed for practical problems. We investigated the link between hydrogen peroxide (H2O2) flux, oxygen influx and seed vigor of Caragana korshinskii by the non-invasive micro-test technique (NMT). Some related physiological and biochemical changes in seeds were also determined to further explain the changes in the molecular fluxes. The results showed that there was a good linear relationship between germination and H2O2 flux, and that O2 influx was more suitable for assessing seed vigor. H2O2 flux changed relatively little initially, mainly affected by antioxidants (APX, CAT and GSH) and H2O2 content; afterward, the efflux increased more and more rapidly due to high membrane permeability. With the damage of mitochondrial respiration and membrane integrity, O2 influx was gradually reduced. We propose that monitoring H2O2 and O2 fluxes by NMT may be a reliable and sensitive method to evaluate seed germination and vigor.

  16. N2O molecular tagging velocimetry

    NASA Astrophysics Data System (ADS)

    ElBaz, A. M.; Pitz, R. W.

    2012-03-01

    A new seeded velocity measurement technique, N2O molecular tagging velocimetry (MTV), is developed to measure velocity in wind tunnels by photochemically creating an NO tag line. Nitrous oxide "laughing gas" is seeded into the air flow. A 193 nm ArF excimer laser dissociates the N2O to O(1D) that subsequently reacts with N2O to form NO. O2 fluorescence induced by the ArF laser "writes" the original position of the NO line. After a time delay, the shifted NO line is "read" by a 226-nm laser sheet and the velocity is determined by time-of-flight. At standard atmospheric conditions with 4% N2O in air, ˜1000 ppm of NO is photochemically created in an air jet based on experiment and simulation. Chemical kinetic simulations predict 800-1200 ppm of NO for 190-750 K at 1 atm and 850-1000 ppm of NO for 0.25-1 atm at 190 K. Decreasing the gas pressure (or increasing the temperature) increases the NO ppm level. The presence of humid air has no significant effect on NO formation. The very short NO formation time (<10 ns) makes the N2O MTV method amenable to low- and high-speed air flow measurements. The N2O MTV technique is demonstrated in air jet to measure its velocity profile. The N2O MTV method should work in other gas flows as well (e.g., helium) since the NO tag line is created by chemical reaction of N2O with O(1D) from N2O photodissociation and thus does not depend on the bulk gas composition.

  17. Potential for negative emissions of greenhouse gases (CO2, CH4 and N2O) through coastal peatland re-establishment: Novel insights from high frequency flux data at meter and kilometer scales

    NASA Astrophysics Data System (ADS)

    Windham-Myers, Lisamarie; Bergamaschi, Brian; Anderson, Frank; Knox, Sara; Miller, Robin; Fujii, Roger

    2018-04-01

    High productivity temperate wetlands that accrete peat via belowground biomass (peatlands) may be managed for climate mitigation benefits due to their global distribution and notably negative emissions of atmospheric carbon dioxide (CO2) through rapid storage of carbon (C) in anoxic soils. Net emissions of additional greenhouse gases (GHG)—methane (CH4) and nitrous oxide (N2O)—are more difficult to predict and monitor due to fine-scale temporal and spatial variability, but can potentially reverse the climate mitigation benefits resulting from CO2 uptake. To support management decisions and modeling, we collected continuous 96 hour high frequency GHG flux data for CO2, CH4 and N2O at multiple scales—static chambers (1 Hz) and eddy covariance (10 Hz)—during peak productivity in a well-studied, impounded coastal peatland in California’s Sacramento Delta with high annual rates of C fluxes, sequestering 2065 ± 150 g CO2 m‑2 y‑1 and emitting 64.5 ± 2.4 g CH4 m‑2 y‑1. Chambers (n = 6) showed strong spatial variability along a hydrologic gradient from inlet to interior plots. Daily (24 hour) net CO2 uptake (NEE) was highest near inlet locations and fell dramatically along the flowpath (‑25 to ‑3.8 to +2.64 g CO2 m‑2 d‑1). In contrast, daily net CH4 flux increased along the flowpath (0.39 to 0.62 to 0.88 g CH4 m‑2 d‑1), such that sites of high daily CO2 uptake were sites of low CH4 emission. Distributed, continuous chamber data exposed five novel insights, and at least two important datagaps for wetland GHG management, including: (1) increasing dominance of CH4 ebullition fluxes (15%–32% of total) along the flowpath and (2) net negative N2O flux across all sites as measured during a 4 day period of peak biomass (‑1.7 mg N2O m‑2 d‑1 0.51 g CO2 eq m‑2 d‑1). The net negative emissions of re-established peat-accreting wetlands are notably high, but may be poorly estimated by

  18. Comparison of methods for the determination of NO-O3-NO2 fluxes and chemical interactions over a bare soil

    NASA Astrophysics Data System (ADS)

    Stella, P.; Loubet, B.; Laville, P.; Lamaud, E.; Cazaunau, M.; Laufs, S.; Bernard, F.; Grosselin, B.; Mascher, N.; Kurtenbach, R.; Mellouki, A.; Kleffmann, J.; Cellier, P.

    2012-06-01

    Tropospheric ozone (O3) is a known greenhouse gas responsible for impacts on human and animal health and ecosystem functioning. In addition, O3 plays an important role in tropospheric chemistry, together with nitrogen oxides. The determination of surface-atmosphere exchange fluxes of these trace gases is a prerequisite to establish their atmospheric budget and evaluate their impact onto the biosphere. In this study, O3, nitric oxide (NO) and nitrogen dioxide (NO2) fluxes were measured using the aerodynamic gradient method over a bare soil in an agricultural field. Ozone and NO fluxes were also measured using eddy-covariance and automatic chambers, respectively. The aerodynamic gradient measurement system, composed of fast response sensors, was capable to measure significant differences in NO and O3 mixing ratios between heights. However, due to local advection, NO2 mixing ratios were highly non-stationary and NO2 fluxes were, therefore, not significantly different from zero. The chemical reactions between O3, NO and NO2 led to little ozone flux divergence between the surface and the measurement height (less than 1% of the flux on average), whereas the NO flux divergence was about 10% on average. The use of fast response sensors allowed reducing the flux uncertainty. The aerodynamic gradient and the eddy-covariance methods gave comparable O3 fluxes. The chamber NO fluxes were down to 70% lower than the aerodynamic gradient fluxes, probably because of either the spatial heterogeneity of the soil NO emissions or the perturbation due to the chamber itself.

  19. 40 CFR 1065.275 - N2O measurement devices.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... for interpretation of infrared spectra. For example, EPA Test Method 320 is considered a valid method... and length to achieve adequate resolution of the N2O peak for analysis. Examples of acceptable columns....550(b) that would otherwise apply. For example, you may perform a span gas measurement before and...

  20. 40 CFR 1065.275 - N2O measurement devices.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... for interpretation of infrared spectra. For example, EPA Test Method 320 is considered a valid method... and length to achieve adequate resolution of the N2O peak for analysis. Examples of acceptable columns....550(b) that would otherwise apply. For example, you may perform a span gas measurement before and...

  1. The Temperature and Structure Dependence of Surface Tension of CaO-SiO2-Na2O-CaF2 Mold Fluxes

    NASA Astrophysics Data System (ADS)

    Gao, Qiang; Min, Yi; Jiang, Maofa

    2018-06-01

    The surface tension of mold flux is one of the most important properties and varies with the temperature from the top to the bottom of the mold, which influences the adhesion and lubrication between the liquid mold flux and the solidified shell, further influencing the quality of the continuous billet. In the present paper, the effect of temperature on the surface tension of CaO-SiO2-Na2O-CaF2 mold-flux melts with different CaO/SiO2 mass ratios was investigated using the maximum-pull method. Furthermore, the microstructure of mold fluxes was analyzed using FT-IR and Raman spectra to discuss the change mechanism of surface tension. The results indicated that the temperature dependence of surface tension was different with different CaO/SiO2 mass ratios, and agreed with the modification of melt structure. When the CaO/SiO2 mass ratio was 0.67 and 0.85, the change of surface tension with temperature was relatively stable, and the influence of temperature on the structure was small. When the CaO/SiO2 mass ratio was 1.03 and 1.16, with an increase of temperature, the surface tension decreased linearly and the changing amplitude was large; the degree of polymerization of melts and average radii of silicon-oxygen anions also decreased, which intensified the molecular thermal motion and weakened the intermolecular interaction, resulting in a decrease of surface tension of melts.

  2. The Temperature and Structure Dependence of Surface Tension of CaO-SiO2-Na2O-CaF2 Mold Fluxes

    NASA Astrophysics Data System (ADS)

    Gao, Qiang; Min, Yi; Jiang, Maofa

    2018-02-01

    The surface tension of mold flux is one of the most important properties and varies with the temperature from the top to the bottom of the mold, which influences the adhesion and lubrication between the liquid mold flux and the solidified shell, further influencing the quality of the continuous billet. In the present paper, the effect of temperature on the surface tension of CaO-SiO2-Na2O-CaF2 mold-flux melts with different CaO/SiO2 mass ratios was investigated using the maximum-pull method. Furthermore, the microstructure of mold fluxes was analyzed using FT-IR and Raman spectra to discuss the change mechanism of surface tension. The results indicated that the temperature dependence of surface tension was different with different CaO/SiO2 mass ratios, and agreed with the modification of melt structure. When the CaO/SiO2 mass ratio was 0.67 and 0.85, the change of surface tension with temperature was relatively stable, and the influence of temperature on the structure was small. When the CaO/SiO2 mass ratio was 1.03 and 1.16, with an increase of temperature, the surface tension decreased linearly and the changing amplitude was large; the degree of polymerization of melts and average radii of silicon-oxygen anions also decreased, which intensified the molecular thermal motion and weakened the intermolecular interaction, resulting in a decrease of surface tension of melts.

  3. Nitrous oxide fluxes from cultivated areas and rangeland: U.S. High Plains

    USGS Publications Warehouse

    Weeks, Edwin P.; McMahon, Peter B.

    2007-01-01

    Concentration profiles of N2O, a greenhouse gas, and the conservative trace gases SF6 and the chlorofluorocarbons CFC-11, CFC-12, CFC-113, and were measured periodically through thick vadose zones at nine sites in the U.S. High Plains. The CFC and SF6 measurements were used to calibrate a one-dimensional gas diffusion model, using the parameter identification program UCODE. The calibrated model was used with N2O measurements to estimate average annual N2O flux from both the root zone and the deep vadose zone to the atmosphere. Estimates of root-zone N 2O fluxes from three rangeland sites ranged from near 0 to about 0.2 kg N2O-N ha-1 yr-1, values near the low end of the ranges determined for native grass from other studies. Estimates of root-zone N2O fluxes from two fields planted to corn (Zea mays L.) of about 2 to 6 kg N2O-N ha-1 yr-1 are similar to those determined for corn in other studies. Estimates of N2O flux from Conservation Reserve grassland converted from irrigated corn indicate that production of N2O is substantially reduced following conversion from cropland. Small N2O fluxes from the water table or from deep in the vadose zone occurred at three sites, ranging from 0.004 to 0.02 kg N 2O-N ha-1 yr-1. Our estimates of N2O flux represent space- and time-averaged values that should be useful to more fully evaluate the significance of instantaneous point flux measurements. ?? Soil Science Society of America.

  4. Photoelectron spectroscopic study of the hydrated nucleoside anions: Uridine(-)(H(2)O)(n=0-2), cytidine(-)(H(2)O)(n=0-2), and thymidine(-)(H(2)O)(n=0,1).

    PubMed

    Li, Xiang; Wang, Haopeng; Bowen, Kit H

    2010-10-14

    The hydrated nucleoside anions, uridine(-)(H(2)O)(n=0-2), cytidine(-)(H(2)O)(n=0-2), and thymidine(-)(H(2)O)(n=0,1), have been prepared in beams and studied by anion photoelectron spectroscopy in order to investigate the effects of a microhydrated environment on parent nucleoside anions. Vertical detachment energies (VDEs) were measured for all eight anions, and from these, estimates were made for five sequential anion hydration energies. Excellent agreement was found between our measured VDE value for thymidine(-)(H(2)O)(1) and its calculated value in the companion article by S. Kim and H. F. Schaefer III.

  5. Photoelectron spectroscopic study of the hydrated nucleoside anions: Uridine-(H2O)n=0-2, cytidine-(H2O)n=0-2, and thymidine-(H2O)n=0,1

    NASA Astrophysics Data System (ADS)

    Li, Xiang; Wang, Haopeng; Bowen, Kit H.

    2010-10-01

    The hydrated nucleoside anions, uridine-(H2O)n=0-2, cytidine-(H2O)n=0-2, and thymidine-(H2O)n=0,1, have been prepared in beams and studied by anion photoelectron spectroscopy in order to investigate the effects of a microhydrated environment on parent nucleoside anions. Vertical detachment energies (VDEs) were measured for all eight anions, and from these, estimates were made for five sequential anion hydration energies. Excellent agreement was found between our measured VDE value for thymidine-(H2O)1 and its calculated value in the companion article by S. Kim and H. F. Schaefer III.

  6. Predicting Coupled Emissions of N2O, CO2 and CH4 from Arable Fields in Ireland Using the ECOSSE Model

    NASA Astrophysics Data System (ADS)

    Khalil, M. I.; Smith, J.; Abdalla, M.; O'Brien, P.; Smith, P.; Müller, C.

    2011-12-01

    Agriculture and associated land-use changes contribute a significant portion to global greenhouse gas (GHG) emissions; mainly as N2O, CO2 and CH4. Improved modelling of soil processes will greatly enhance the value of national inventories, both in terms of more accurate reporting and better mitigation policy options. In Ireland, Agriculture and Land Use, Land Use Change and Forestry, is currently a priority research focus, aimed at reducing uncertainty in estimates of GHG emissions and sinks. The ECOSSE model has several advantages, including limited meteorological and soil data requirements, compared to other models. It can simulate the impacts of land-use, management and climate change on C and N emissions and stocks for both mineral and organic soils at field and national scales. In this study, ECOSSE has been used to predict GHG emissions and SOC changes in arable lands cropped with spring barley receiving different rates of N application. The simulated outputs are evaluated against measured data available from a two-year field study. The modelled responses of N2O fluxes are found to be consistent with the measured values. The bias in the total difference between measured values and the corresponding modelled N2O fluxes was large due to the impact of a few unexpected measurements. In the fertilized fields, significant correlation between modelled and measured N2O fluxes was observed, with correlation coefficients of 0.54-0.60 and root mean square errors of 18.6-20.8 g N ha-1 d-1. The measured seasonal (crop growth period) N2O losses (integrated) were 0.41 and 0.50% of the N applied at rates of 70-79 and 140-159 kg ha-1, respectively. As a further comparison, the simulated values for the dates when measurements were taken were similarly integrated. The corresponding simulated seasonal N2O losses were 0.69 and 1.11% of the added N, suggesting an overestimation by 70-123% of the measured values. However, this could be due to missed emissions associated with the

  7. DMPP-added nitrogen fertilizer affects soil N2O emission and microbial activity in Southern Italy

    NASA Astrophysics Data System (ADS)

    Vitale, Luca; De Marco, Anna; Maglione, Giuseppe; Polimeno, Franca; Di Tommasi, Paul; Magliulo, Vincenzo

    2014-05-01

    Arable sites contributes to global N2O emission due to massive utilization of nitrogen fertilizers. N2O derives from the biological processes such as nitrification and denitrification influenced by soil nitrogen availability. The use of nitrogen fertilizers added with nitrification inhibitors represents one among the proposed strategy to reduce soil N2O emission form arable sites. The aim of this work was to evaluate the effects of 3,4-dimethylphyrazole phosphate (DMPP), a nitrification inhibitor, on N2O emission and microbial activity of a soil cropped to potato in Southern Italy. The experiment was a randomized block design with two treatments applied and three replicates: control (C) and DMPP (Entec®, K+S Nitrogen) plots, both supplied with the same amount of ammonium nitrate. The nitrogen fertilizer was supplied in three events: at 0 Day After Sowing (DAS; 100 kg N ha-1), at 57 DAS (30 kg N ha-1), and at 71 DAS (30 kg N ha-1). Soil N2O emission was monitored by both dynamic and static chambers. Static chambers were located both on hills and furrows whereas dynamic chambers were located on furrows. Air samples were collected from chambers at different times and analysed by a gas chromatograph (SRI 8610C, Gas Chromatograph). Fluxes were estimated as a linear interpolation of N2O changes over a 30 min time. Microbial biomass and basal respiration were determined as CO2 evolution, analysed by means of an IRGA (Li6200, Licor), on 2 g of fresh soil over a 4h incubation time. Microbial biomass was determined by Substrate Induced Respiration method. Data show no statistical differences in N2O fluxes measured with either dynamic chambers between C and DMPP plots in studied period. However, after the first fertilization event, when the fertilizer was applied as 100 kg N ha-1, the average N2O fluxes measured with static chambers were higher in DMPP plots compared to C plots. In the same period, the microbial biomass significantly decreased in DMPP plots as compared to C

  8. Grasland Stable Isotope Flux Measurements: Three Isotopomers of Carbon Dioxide Measured by QCL Spectroscopy

    NASA Astrophysics Data System (ADS)

    Zeeman, M. J.; Tuzson, B.; Eugster, W.; Werner, R. A.; Buchmann, N.; Emmenegger, L.

    2007-12-01

    To improve our understanding of greenhouse gas dynamics of managed ecosystems such as grasslands, we not only need to investigate the effects of management (e.g., grass cuts) and weather events (e.g., rainy days) on carbon dioxide fluxes, but also need to increase the time resolution of our measurements. Thus, for the first time, we assessed respiration and assimilation fluxes with high time resolution (5Hz) stable isotope measurements at an intensively managed farmland in Switzerland (Chamau, 400m ASL). Two different methods were used to quantify fluxes of carbon dioxide and associated fluxes of stable carbon isotopes: (1) the flux gradient method, and (2) the eddy covariance method. During a week long intensive measurement campaign, we (1) measured mixing ratios of carbon dioxide isotopomers (12C16O2, 12C16O18O, 13C16O2) with a Quantum Cascade Laser (QCL, Aerodyne Inc.) spectroscope and (2) collected air samples for isotope analyses (13C/12C) and (18O/16O) of carbon dioxide by Isotope Ratio Mass Spectrometry (IRMS, Finnigan) every two hours, concurrently along a height profile (z = 0.05; 0.10; 0.31; 2.15m). In the following week, the QCL setup was used for closed-path eddy covariance flux measurement of the carbon dioxide isotopomers, with the air inlet located next to an open-path Infra Red Gas Analyzers (IRGA, LiCor 7500) used simultaneously for carbon dioxide measurements. During this second week, an area of grass inside the footprint was cut and harvested after several days. The first results of in-field continuous QCL measurements of carbon dioxide mixing ratios and their stable isotopic ratios show good agreement with IRGA measurements and isotope analysis of flask samples by IRMS. Thus, QCL spectroscopy is a very promising tool for stable isotope flux investigations.

  9. Heterodyne frequency measurements on N2O at 5.3 and 9.0 microns

    NASA Technical Reports Server (NTRS)

    Wells, J. S.; Jennings, D. A.; Hinz, A.; Murray, J. S.; Maki, A. G.

    1985-01-01

    Heterodyne frequency measurements on the 01(1)1-00(0)0 band of N2O have been made with the use of a tunable-diode laser, CO laser transfer oscillator, and a CO2 laser frequency synthesizer. A beat frequency was measured between a CO laser and tunable-diode laser whose frequency was locked to the peak of N2O absorption features. The frequency of the CO laser was simultaneously determined by neasuring the beat frequency with respect to a reference synthesized from two CO2 lasers. New rovibrational constants are given for the 01(1)1 state of N2O, which are in excellent agreement with previous results, although the band center is 4 MHz higher than in the previous measurements. A table for the line frequencies and their absolute uncertainties is given for the N2O absorption lines in the wave-number region from 1830 to 1920 kaysers. Some additional frequency measurements near the lower-frequency end of the 02(0)0-00(0)0 band have also been made with respect to a C-12)(0-18)2 laser.

  10. Year-round N2O production by benthic NOx reduction in a monomictic south-alpine lake

    NASA Astrophysics Data System (ADS)

    Freymond, C. V.; Wenk, C. B.; Frame, C. H.; Lehmann, M. F.

    2013-12-01

    Nitrous oxide (N2O) is a potent greenhouse gas, generated through microbial nitrogen (N) turnover processes, such as nitrification, nitrifier denitrification, and denitrification. Previous studies quantifying natural sources have mainly focused on soils and the ocean, but the potential role of terrestrial water bodies in the global N2O budget has been widely neglected. Furthermore, the biogeochemical controls on the production rates and the microbial pathways that produce benthic N2O in lakes are essentially unknown. In this study, benthic N2O fluxes and the contributions of the microbial pathways that produce N2O were assessed using 15N label flow-through sediment incubations in the eutrophic, monomictic south basin of Lake Lugano in Switzerland. The sediments were a significant source of N2O throughout the year, with production rates ranging between 140 and 2605 nmol N2O h-1 m-2, and the highest observed rates coinciding with periods of water column stratification and stably anoxic conditions in the overlying bottom water. Nitrate (NO3-) reduction via denitrification was found to be the major N2O production pathway in the sediments under both oxygen-depleted and oxygen-replete conditions in the overlying water, while ammonium oxidation did not contribute significantly to the benthic N2O flux. A marked portion (up to 15%) of the total NO3- consumed by denitrification was reduced only to N2O, without complete denitrification to N2. These fluxes were highest when the bottom water had stabilized to a low-oxygen state, in contrast with the notion that stable anoxia is particularly conducive to complete denitrification without accumulation of N2O. This study provides evidence that lake sediments are a significant source of N2O to the overlying water and may produce large N2O fluxes to the atmosphere during seasonal mixing events.

  11. Characterization of the N2O isotopic composition (15N, 18O and N2O isotopomers) emitted from incubated Amazon forest soils. Implications for the global N2O isotope budget

    NASA Astrophysics Data System (ADS)

    Pérez, T.; García, D.; Trumbore, S.; Tyler, S.; de Camargo, P.; Moreira, M.; Piccolo, M.; Park, S.; Boering, K.; Cerri, C.

    2003-04-01

    Tropical rain forest soils are the largest natural source of N2O to the atmosphere. Uncertainty in the signature of this source limits the utility of isotopes in constraining the global N2O budget. Differentiating the relative contribution of nitrification and denitrification to the emitted N2O using stable isotopes has been difficult due to the lack of enrichment factors values for each process measured in situ. We have devised a method for measuring enrichment factors using soil incubation experiments. We selected three Amazon rain forest soils: (1) Clay and (2) Sandy from Santarem, Pará State, and (3) Sandy from Nova Vida Farm, Rondonia State, Brazil. The enrichment factor values for nitrification and denitrification are: -97.8±4.2 and -9.9±3.8 per mil for clay Santarem soil, -86.8±4.3 and -45.2±4.5 per mil for sandy Santarem soil and-112.6±3.8 and -10.4±3.5 per mil for Nova Vida Farm soils, respectively. Our results show that enrichment factors for both processes differ with soil texture and location. The enrichment factors for nitrification are significantly smaller than the range reported in the literature (-66 to -42 per mil). Also, the enrichment factors for the Santarem soils (clay and sandy) differ significantly implying that soil texture (which will affect the soil air filled pore space at a given water content) is influencing the bacteria isotopic discrimination. However, the enrichment factors for the Santarem clay sand Nova Vida sandy soils do not differ by much. This suggests that the enrichment factors not only can be affected by texture but also by the microbial fauna present in these soils. We also determined the measurement of the N2O positional dependence. N2O is a linear molecule with two nitrogen atoms. The 15N isotope can be located in either the central nitrogen (alpha position) or in the terminal nitrogen (beta position). The isotopomer site preference (15N alpha - 15N beta) can be used to differentiate processes of production and

  12. Micrometeorological flux measurements at a coastal site

    NASA Astrophysics Data System (ADS)

    Song, Guozheng; Meixner, Franz X.; Bruse, Michael; Mamtimin, Buhalqem

    2014-05-01

    The eddy covariance (EC) technique is the only direct measurement of the momentum, heat, and trace gas (e.g. water vapor, CO2 and ozone) fluxes. The measurements are expected to be most accurate over flat terrain where there is an extended homogenous surface upwind from the tower, and when the environmental conditions are steady. Additionally, the one dimensional approach assumes that vertical turbulent exchange is the dominant flux, whereas advective influences should be negligible. The application of EC method under non-ideal conditions, for example in complex terrain, has yet to be fully explored. To explore the possibilities and limitations of EC technique under non-ideal conditions, an EC system was set up at Selles beach, Crete, Greece (35.33°N, 25.71°E) in the beginning of July 2012. The dominant wind direction was west, parallel to the coast. The EC system consisted of a sonic anemometer (CSAT3 Campbell Scientific), an infrared open-path CO2/H2O gas analyzer (LI-7500, Li-COR Biosciences) and a fast chemiluminescence ozone analyzer (enviscope GmbH). All the signals of these fast response instruments were sampled at 10 Hz and the measurement height was 3 m. Besides, another gradient system was setup. Air temperature, relative humidity (HYGROMER MP 103 A), and wind speed (WMT700 Vaisala) were measured every 10 seconds at 3 heights (0.7, 1.45, 3 m). Air intakes were set up at 0.7m and 3m. A pump drew the air through a flow system and a telflon valve alternately switched between the two heights every 30 seconds. H2O, CO2 (LI-840A, Li-COR Biosciences) and ozone mixing ratio s (model 205, 2BTechnologies) were measured every 10 seconds. Momentum, heat, CO2 and ozone fluxes were evaluated by both EC and gradient technique. For the calculation of turbulent fluxes, TK3 algorithm (Department of Micrometeorology, University Bayreuth, Germany) was applied. We will present the measured fluxes of the two systems and assess the data quality under such non-ideal condition.

  13. Soil Emissions of N2O and NO in Agricultural Production Systems in the Upper Midwest U.S.: Management Controls and Measurement Issues (Invited)

    NASA Astrophysics Data System (ADS)

    Venterea, R. T.; Baker, J. M.

    2009-12-01

    Cropped fields in the upper Midwest have the potential to emit relatively large quantities of N2O and NO resulting from soil transformation of N fertilizers applied to crops such as corn and potatoes. The mitigation of N2O emissions may be an effective strategy for offsetting greenhouse gas emissions. While the rate of N fertilizer application exerts some control over N trace gas emission rates, a variety of other management practices and environmental factors interact to regulate these emissions. Observation-based studies are essential for improving models, developing accurate inventories, and documenting offsets. Since 2003, we have been examining the effects of management factors including: tillage, crop rotation, irrigation, and fertilizer chemical form and application method on N2O and NO emissions from corn and potato production systems using chamber-based measurement techniques. A summary of our findings will be presented, including: Application of anhydrous ammonia resulted in twice the N2O emissions compared to urea fertilizer, and twice the NO emissions compared to liquid urea ammonium nitrate (UAN) fertilizer. Growing corn continuously compared to in rotation with soybeans did not alter the amount of N2O emitted during the corn growing season. Reduced tillage (RT), often promoted as a means of reducing carbon losses to the atmosphere, also altered soil N2O emissions. However, the impact of RT on N2O emissions was found to vary, in both magnitude and direction, as a function of N fertilizer management. In addition to these studies, our efforts to overcome some of the inherent limitations of chamber-based flux measurement techniques will be discussed.

  14. Simulated nitrogen deposition reduces CH4 uptake and increases N2O emission from a subtropical plantation forest soil in southern China.

    PubMed

    Wang, Yongsheng; Cheng, Shulan; Fang, Huajun; Yu, Guirui; Xu, Minjie; Dang, Xusheng; Li, Linsen; Wang, Lei

    2014-01-01

    To date, few studies are conducted to quantify the effects of reduced ammonium (NH4+) and oxidized nitrate (NO3-) on soil CH4 uptake and N2O emission in the subtropical forests. In this study, NH4Cl and NaNO3 fertilizers were applied at three rates: 0, 40 and 120 kg N ha(-1) yr(-1). Soil CH4 and N2O fluxes were determined twice a week using the static chamber technique and gas chromatography. Soil temperature and moisture were simultaneously measured. Soil dissolved N concentration in 0-20 cm depth was measured weekly to examine the regulation to soil CH4 and N2O fluxes. Our results showed that one year of N addition did not affect soil temperature, soil moisture, soil total dissolved N (TDN) and NH4+-N concentrations, but high levels of applied NH4Cl and NaNO3 fertilizers significantly increased soil NO3(-)-N concentration by 124% and 157%, respectively. Nitrogen addition tended to inhibit soil CH4 uptake, but significantly promoted soil N2O emission by 403% to 762%. Furthermore, NH4+-N fertilizer application had a stronger inhibition to soil CH4 uptake and a stronger promotion to soil N2O emission than NO3(-)-N application. Also, both soil CH4 and N2O fluxes were driven by soil temperature and moisture, but soil inorganic N availability was a key integrator of soil CH4 uptake and N2O emission. These results suggest that the subtropical plantation soil sensitively responses to atmospheric N deposition, and inorganic N rather than organic N is the regulator to soil CH4 uptake and N2O emission.

  15. The 2017 Fertilizer Emissions Airborne Study (FEAST): Quantifying N2O emissions from croplands and fertilizer plants in the Mississippi River Valley.

    NASA Astrophysics Data System (ADS)

    Kort, E. A.; Gvakharia, A.; Smith, M. L.; Conley, S.; Frauhammer, K.

    2017-12-01

    Nitrous Oxide (N2O) is a crucial atmospheric trace gas that drives 21st century stratospheric ozone depletion and substantively impacts climate. Anthropogenic emissions drive the global imbalance and annual growth of N2O, and the dominant anthropogenic source is fertilizer production and application, both of which have large uncertainties. In this presentation we will discuss the FEAST campaign, a study designed to demonstrate new approaches to quantify N2O emissions from fertilizer production and usage with aircraft measurements. In the FEAST campaign we deployed new instrumentation along with experienced flight sensors onboard the Scientific Aviation Mooney aircraft to make 40 hours of continuous 1Hz measurements of N2O, CO2, CO, H2O, CH4, O3, T, and winds. The Mississippi River Valley provided an optimal target as this location includes significant fertilizer production facilities as well as large cropland areas (dominated by corn, soy, rice, and cotton) with substantive fertilizer application. By leveraging our payload and unique airborne capabilities we directly observe and quantify N2O emissions from individual fertilizer production facilities (as well as CO2 and CH4 emissions from these same facilities). We are also able to quantify N2O fluxes from large cropland areas ( 100's km) employing a mass balance approach, a first for N2O, and will show results highlighting differences between crop types and amounts of applied fertilizer. The ability to quantify fluxes of croplands at 100km scale enables new understanding of processes controlling emissions at spatial scales that has eluded prior studies that either rely on extrapolation of small (flux chamber, towers), or work on 1,000+ km spatial scales (regional-global inversions from atmospheric measurements).

  16. Flooding-related increases in CO2 and N2O emissions from a temperate coastal grassland ecosystem

    NASA Astrophysics Data System (ADS)

    Gebremichael, Amanuel W.; Osborne, Bruce; Orr, Patrick

    2017-05-01

    Given their increasing trend in Europe, an understanding of the role that flooding events play in carbon (C) and nitrogen (N) cycling and greenhouse gas (GHG) emissions will be important for improved assessments of local and regional GHG budgets. This study presents the results of an analysis of the CO2 and N2O fluxes from a coastal grassland ecosystem affected by episodic flooding that was of either a relatively short (SFS) or long (LFS) duration. Compared to the SFS, the annual CO2 and N2O emissions were 1.4 and 1.3 times higher at the LFS, respectively. Mean CO2 emissions during the period of standing water were 144 ± 18.18 and 111 ± 9.51 mg CO2-C m-2 h-1, respectively, for the LFS and SFS sites. During the growing season, when there was no standing water, the CO2 emissions were significantly larger from the LFS (244 ± 24.88 mg CO2-C m-2 h-1) than the SFS (183 ± 14.90 mg CO2-C m-2 h-1). Fluxes of N2O ranged from -0.37 to 0.65 mg N2O-N m-2 h-1 at the LFS and from -0.50 to 0.55 mg N2O-N m-2 h-1 at the SFS, with the larger emissions associated with the presence of standing water at the LFS but during the growing season at the SFS. Overall, soil temperature and moisture were identified as the main drivers of the seasonal changes in CO2 fluxes, but neither adequately explained the variations in N2O fluxes. Analysis of total C, N, microbial biomass and Q10 values indicated that the higher CO2 emissions from the LFS were linked to the flooding-associated influx of nutrients and alterations in soil microbial populations. These results demonstrate that annual CO2 and N2O emissions can be higher in longer-term flooded sites that receive significant amounts of nutrients, although this may depend on the restriction of diffusional limitations due to the presence of standing water to periods of the year when the potential for gaseous emissions are low.

  17. Nitrous oxide fluxes from tree stems of temperate forests

    NASA Astrophysics Data System (ADS)

    Wen, Yuan; Corre, Marife D.; Rachow, Christine; Veldkamp, Edzo

    2017-04-01

    Although trees are recognized as conduits of soil-generated N2O, little is known about N2O fluxes from mature trees under field conditions and thier contributions to total forest N2O fluxes. Here, we quantified in situ stem N2O fluxes from mature alder trees on poorly-drained soil and mature beech and spruce trees on well-drained soils in Solling, Germany from March to October 2015. Soil N2O fluxes, soil N2O concentrations at 40-cm depth, and soil and climatic variables known to influence N2O fluxes were also measured concurrently with the stem N2O fluxes. Alder, beech and spruce consistently emitted N2O via stems and all displayed higher emission rates in summer than in spring and in autumn. Stem N2O fluxes from alder stand were higher than those from beech and spruce stands (P < 0.01), which was attributed to the presence of aerenchyma and lenticels as well as higher soil water content and soil C and N availability in the alder stand (P < 0.01-0.05). The correlations of stem N2O fluxes from alder with soil N2O fluxes, soil N2O concentrations, soil and air temperature and vapor pressure deficit (R = 0.60 - 0.90, P < 0.01-0.05) suggest that N2O transport in alder was facilitated by a combination of passive gas diffusion through aerenchyma and active transport of dissolved N2O through sap flow. In the beech and spruce stands, correlations of stem N2O fluxes with soil and air temperature and vapor pressure deficit (R = 0.57 - 0.78, P < 0.01-0.07) suggest that active transport of dissolved N2O via xylem sap was the major mechanism for stem N2O emissions in upland trees. Stem N2O fluxes represented 8-11% of the total (soil + stem) N2O fluxes in the spruce and beech stands whereas in the alder stand, with its large soil N2O emission, stem emission contributed only 1% of the total flux. Our results suggest that the relative contribution of tree-mediated N2O fluxes is more important in upland trees than in wetland trees.

  18. Wavelength-dependent UV photodesorption of pure N2 and O2 ices

    NASA Astrophysics Data System (ADS)

    Fayolle, E. C.; Bertin, M.; Romanzin, C.; Poderoso, H. A. M.; Philippe, L.; Michaut, X.; Jeseck, P.; Linnartz, H.; Öberg, K. I.; Fillion, J.-H.

    2013-08-01

    Context. Ultraviolet photodesorption of molecules from icy interstellar grains can explain observations of cold gas in regions where thermal desorption is negligible. This non-thermal desorption mechanism should be especially important where UV fluxes are high. Aims: N2 and O2 are expected to play key roles in astrochemical reaction networks, both in the solid state and in the gas phase. Measurements of the wavelength-dependent photodesorption rates of these two infrared-inactive molecules provide astronomical and physical-chemical insights into the conditions required for their photodesorption. Methods: Tunable radiation from the DESIRS beamline at the SOLEIL synchrotron in the astrophysically relevant 7 to 13.6 eV range is used to irradiate pure N2 and O2 thin ice films. Photodesorption of molecules is monitored through quadrupole mass spectrometry. Absolute rates are calculated by using the well-calibrated CO photodesorption rates. Strategic N2 and O2 isotopolog mixtures are used to investigate the importance of dissociation upon irradiation. Results: N2 photodesorption mainly occurs through excitation of the b1Πu state and subsequent desorption of surface molecules. The observed vibronic structure in the N2 photodesorption spectrum, together with the absence of N3 formation, supports that the photodesorption mechanism of N2 is similar to CO, i.e., an indirect DIET (Desorption Induced by Electronic Transition) process without dissociation of the desorbing molecule. In contrast, O2 photodesorption in the 7-13.6 eV range occurs through dissociation and presents no vibrational structure. Conclusions: Photodesorption rates of N2 and O2 integrated over the far-UV field from various star-forming environments are lower than for CO. Rates vary between 10-3 and 10-2 photodesorbed molecules per incoming photon.

  19. Using stable isotopes to follow excreta N dynamics and N2O emissions in animal production systems.

    PubMed

    Clough, T J; Müller, C; Laughlin, R J

    2013-06-01

    Nitrous oxide (N2O) is a potent greenhouse gas and the dominant anthropogenic stratospheric ozone-depleting emission. The tropospheric concentration of N2O continues to increase, with animal production systems constituting the largest anthropogenic source. Stable isotopes of nitrogen (N) provide tools for constraining emission sources and, following the temporal dynamics of N2O, providing additional insight and unequivocal proof of N2O source, production pathways and consumption. The potential for using stable isotopes of N is underutilised. The intent of this article is to provide an overview of what these tools are and demonstrate where and how these tools could be applied to advance the mitigation of N2O emissions from animal production systems. Nitrogen inputs and outputs are dominated by fertiliser and excreta, respectively, both of which are substrates for N2O production. These substrates can be labelled with 15N to enable the substrate-N to be traced and linked to N2O emissions. Thus, the effects of changes to animal production systems to reduce feed-N wastage by animals and fertiliser wastage, aimed at N2O mitigation and/or improved animal or economic performance, can be traced. Further 15N-tracer studies are required to fully understand the dynamics and N2O fluxes associated with excreta, and the biological contribution to these fluxes. These data are also essential for the new generation of 15N models. Recent technique developments in isotopomer science along with stable isotope probing using multiple isotopes also offer exciting capability for addressing the N2O mitigation quest.

  20. Investigation of N2O Production from 266 and 532 nm Laser Flash Photolysis of O3/N2/O2 Mixtures

    NASA Technical Reports Server (NTRS)

    Estupinan, E. G.; Nicovich, J. M.; Li, J.; Cunnold, D. M.; Wine, P. H.

    2002-01-01

    Tunable diode laser absorption spectroscopy has been employed to measure the amount of N2O produced from laser flash photolysis of O3/N2/O2 mixtures at 266 and 532 nm. In the 532 nm photolysis experiments very little N2O is observed, thus allowing an upper limit yield of 7 x 10(exp -8) to be established for the process O3 + N2 yield N2O + O2, where O3 is nascent O3 that is newly formed via O(3P(sub J)) + O2 recombination (with vibrational excitation near the dissociation energy of O3). The measured upper limit yield is a factor of approx. 600 smaller than a previous literature value and is approximately a factor of 10 below the threshold for atmospheric importance. In the 266 nm photolysis experiments, significant N2O production is observed and the N2O quantum yield is found to increase linearly with pressure over the range 100 - 900 Torr in air bath gas. The source of N2O in the 266 nm photolysis experiments is believed to be the addition reaction O(1D(sub 2)) + N2 + M yields (k(sub sigma)) N2O + M, although reaction of (very short-lived) electronically excited O3 with N2 cannot be ruled out by the available data. Assuming that all observed N2O comes from the O(1D(sub 2)) + N2 + M reaction, the following expression describes the temperature dependence of k(sub sigma) (in its third-order low-pressure limit) that is consistent with the N2O yield data: k(sub sigma) = (2.8 +/- 0.1) x 10(exp -36)(T/300)(sup -(0-88+0.36)) cm(sup 6) molecule(sup -2)/s, where the uncertainties are 2(sigma) and represent precision only. The accuracy of the reported rate coefficients at the 95% confidence level is estimated to be 30 - 40% depending on the temperature. Model calculations suggest that gas phase processes initiated by ozone absorption of a UV photon represent about 1.4% of the currently estimated global source strength of atmospheric N2O. However, these processes could account for a significant fraction of the oxygen mass-independent enrichment observed in atmospheric N2O, and

  1. Assessment of online monitoring strategies for measuring N2O emissions from full-scale wastewater treatment systems.

    PubMed

    Marques, Ricardo; Rodriguez-Caballero, A; Oehmen, Adrian; Pijuan, Maite

    2016-08-01

    Clark-Type nitrous oxide (N2O) sensors are routinely used to measure dissolved N2O concentrations in wastewater treatment plants (WWTPs), but have never before been applied to assess gas-phase N2O emissions in full-scale WWTPs. In this study, a full-scale N2O gas sensor was tested and validated for online gas measurements, and assessed with respect to its linearity, temperature dependence, signal saturation and drift prior to full-scale application. The sensor was linear at the concentrations tested (0-422.3, 0-50 and 0-10 ppmv N2O) and had a linear response up to 2750 ppmv N2O. An exponential correlation between temperature and sensor signal was described and predicted using a double exponential equation while the drift did not have a significant influence on the signal. The N2O gas sensor was used for online N2O monitoring in a full-scale sequencing batch reactor (SBR) treating domestic wastewater and results were compared with those obtained by a commercial online gas analyser. Emissions were successfully described by the sensor, being even more accurate than the values given by the commercial analyser at N2O concentrations above 500 ppmv. Data from this gas N2O sensor was also used to validate two models to predict N2O emissions from dissolved N2O measurements, one based on oxygen transfer rate and the other based on superficial velocity of the gas bubble. Using the first model, predictions for N2O emissions agreed by 98.7% with the measured by the gas sensor, while 87.0% similarity was obtained with the second model. This is the first study showing a reliable estimation of gas emissions based on dissolved N2O online data in a full-scale wastewater treatment facility. Copyright © 2016 Elsevier Ltd. All rights reserved.

  2. Eddy Covariance measurements of stable CO2 and H2O isotopologues

    NASA Astrophysics Data System (ADS)

    Braden-Behrens, Jelka; Knohl, Alexander

    2015-04-01

    The analysis of the stable isotope composition of CO2 and H2O fluxes (such as 13C, 18O and 2H in H2O and CO2) has provided valuable insights into ecosystem gas exchange. The approach builds on differences in the isotope signature of different ecosystem components that are primarily caused by the preference for or the discrimination against respective isotope species by important processes within the ecosystem (e.g. photosynthesis or leaf water diffusion). With the ongoing development of laser spectrometric methods, fast and precise measurements of isotopologue mixing ratios became possible, hence also enabling Eddy Covariance (EC) based approaches to directly measure the isotopic composition of CO2 and H2Ov net fluxes on ecosystem scale. During an eight month long measurement campaign in 2015, we plan to simultaneously measure CO2 and H2Ov isotopologue fluxes using an EC approach in a managed beech forest in Thuringia, Germany. For this purpose, we will use two different laser spectrometers for high frequency measurements of isotopic compositions: For H2Ov measurements, we will use an off axis cavity output water vapour isotope analyser (WVIA, Los Gatos Research Inc.) with 5 Hz response; and for CO2 measurements, we will use a quantum cascade laser-based system (QCLAS, Aerodyne Research Inc.) with thermoelectrically cooled detectors and up to 10 Hz measurement capability. The resulting continuous isotopologue flux measurements will be accompanied by intensive sampling campaigns on the leaf scale: Water from leaf, twig, soil and precipitation samples will be analysed in the lab using isotope ratio mass spectrometry. During data analysis we will put a focus on (i) the influence of carbon and oxygen discrimination on the isotopic signature of respective net ecosystem exchange, (ii) on the relationship between evapotranspiration and leaf water enrichment, and (iii) on the 18O exchange between carbon dioxide and water. At present, we already carried out extensive

  3. Under-recognized pathways of N2O production in coastal sediments: Increased fungal and chemo-denitrification in response to elevated N loading

    NASA Astrophysics Data System (ADS)

    Wankel, S. D.; Ziebis, W.; Buchwald, C.; Charoenpong, C.; de Beer, D.

    2016-02-01

    Increasing atmospheric levels of nitrous oxide (N2O), a greenhouse gas with a 100-year global warming potential more than 300 times that of carbon dioxide, have been strongly linked to human activities - especially the dramatic increase in nitrogen loading to aquatic and marine ecosystems worldwide. While many studies have demonstrated that N2O is formed through a number of microbially mediated pathways, the factors regulating the emission of N2O to the atmosphere remain difficult to predict and the global N2O budget remains poorly constrained. In particular, coastal ecosystems, which bear much of the brunt of anthropogenically-derived nitrogen from watershed inputs and rapidly growing coastal human populations, represent large gaps in our understanding of sources and sinks of atmospheric N2O. In large part, these challenges stem from the fact that a diverse number of N2O production pathways are operative under the dynamic redox conditions encountered in coastal and estuarine sediments, complicating our ability to understand their relative roles in N2O fluxes. Here, we use whole-core sediment incubations together with a suite of conventional and novel stable isotopic tools to identify both factors influencing N2O flux as well as those underlying biogeochemical processes responding to those factors. We find that under elevated N loading to coastal sediments, an observed increase in N2O flux to the overlying water is not mediated by direct bacterial activity, but instead is catalyzed by fungal denitrification and/or abiotic interactions with reduced iron (e.g., chemodenitrification). These findings shed new light on the complexity of nitrogen cycling in coastal sedimentary environments and highlight the need for an improved understanding of eukaryotic and abiotic processes in regulating fluxes of climatically important gases such as N2O.

  4. Influence of Ar/O2/H2O Feed Gas and N2/O2/H2O Environment on the Interaction of Time Modulated MHz Atmospheric Pressure Plasma Jet (APPJ) with Model Polymers

    NASA Astrophysics Data System (ADS)

    Oehrlein, Gottlieb; Luan, Pingshan; Knoll, Andrew; Kondeti, Santosh; Bruggeman, Peter

    2016-09-01

    An Ar/O2/H2O fed time modulated MHz atmospheric pressure plasma jet (APPJ) in a sealed chamber was used to study plasma interaction with model polymers (polystyrene, poly-methyl methacrylate, etc.). The amount of H2O in the feed gas and/or present in the N2, O2, or N2/O2 environment was controlled. Short lived species such as O atoms and OH radicals play a crucial role in polymer etching and surface modifications (obtained from X-ray photoelectron spectroscopy of treated polymers without additional atmospheric exposure). Polymer etching depth for Ar/air fed APPJ mirrors the decay of gas phase O atoms with distance from the APPJ nozzle in air and is consistent with the estimated O atom flux at the polymer surface. Furthermore, whereas separate O2 or H2O admixture to Ar enhances polymer etching, simultaneous addition of O2 and H2O to Ar quenches polymer etching. This can be explained by the mutual quenching of O with OH, H and HO2 in the gas phase. Results where O2 and/or H2O in the environment were varied are consistent with these mechanisms. All results will be compared with measured and simulated species densities reported in the literature. We gratefully acknowledge funding from US Department of Energy (DE-SC0001939) and National Science Foundation (PHY-1415353).

  5. Solar flux variability and the lifetimes of cometary H2O and OH

    NASA Astrophysics Data System (ADS)

    Budzien, S. A.; Festou, M. C.; Feldman, P. D.

    1994-01-01

    A solar EUV/FUV flux model based on recent SUSIM solar observations is presented. It is shown that both the fluxes and variabilities of the model are more consistent with SME and SUSIM solar spectrum measurements than those of the SERF1 model. It is calculated that photodissociation accounts for about 80 percent of the H2O destruction rate, while photoionization and solar wind particle interactions each account for about 10 percent of the H2O destruction. The calculated H2O and OH lifetimes against direct photodissociation both vary by 30 percent with solar activity. The major destruction channel for OH is predissociation, while direct photodissociation and solar wind interactions account for roughly 30 and 10 percent of the destruction rate, respectively.

  6. Influence of Lumbricus terrestris and Folsomia candida on N2 O formation pathways in two different soils - with particular focus on N2 emissions.

    PubMed

    Schorpp, Quentin; Riggers, Catharina; Lewicka-Szczebak, Dominika; Giesemann, Anette; Well, Reinhard; Schrader, Stefan

    2016-11-15

    The gaseous N losses mediated by soil denitrifiers are generally inferred by measuring N 2 O fluxes, but should include associated N 2 emissions, which may be affected by abiotic soil characteristics and biotic interactions. Soil fauna, particularly anecic earthworms and euedaphic collembola, alter the activity of denitrifiers, creating hotspots for denitrification. These soil fauna are abundant in perennial agroecosystems intended to contribute to more sustainable production of bioenergy. Two microcosm experiments were designed to evaluate gaseous N emissions from a silty loam and a sandy soil, both provided with litter from the bioenergy crop Silphium perfoliatum (cup-plant) and inoculated with an anecic earthworm (Lumbricus terrestris), which was added alone or together with an euedaphic collembola (Folsomia candida). In experiment 1, litter-derived N flux was determined by adding 15 N-labelled litter, followed by mass spectrometric analysis of N 2 and N 2 O isotopologues. In experiment 2, the δ 18 O values and 15 N site preference of N 2 O were determined by isotope ratio mass spectrometry to reveal underlying N 2 O formation pathways. Lumbricus terrestris significantly increased litter-derived N 2 emissions in the loamy soil, from 174.5 to 1019.3 μg N 2 -N kg -1 soil, but not in the sandy soil (non-significant change from 944.7 to 1054.7 μg N 2 -N kg -1 soil). Earthworm feeding on plant litter resulted in elevated N 2 O emissions in both soils, derived mainly from turnover of the soil mineral N pool during denitrification. Folsomia candida did not affect N losses but showed a tendency to redirect N 2 O formation pathways from fungal to bacterial denitrification. The N 2 O/(N 2  + N 2 O) product ratio was predominantly affected by abiotic soil characteristics (loamy soil: 0.14, sandy soil: 0.26). When feeding on S. perfoliatum litter, the anecic L. terrestris, but not the euedaphic F. candida, has the potential to cause substantial N losses. Biotic

  7. Constraining a complex biogeochemical model for CO2 and N2O emission simulations from various land uses by model-data fusion

    NASA Astrophysics Data System (ADS)

    Houska, Tobias; Kraus, David; Kiese, Ralf; Breuer, Lutz

    2017-07-01

    This study presents the results of a combined measurement and modelling strategy to analyse N2O and CO2 emissions from adjacent arable land, forest and grassland sites in Hesse, Germany. The measured emissions reveal seasonal patterns and management effects, including fertilizer application, tillage, harvest and grazing. The measured annual N2O fluxes are 4.5, 0.4 and 0.1 kg N ha-1 a-1, and the CO2 fluxes are 20.0, 12.2 and 3.0 t C ha-1 a-1 for the arable land, grassland and forest sites, respectively. An innovative model-data fusion concept based on a multicriteria evaluation (soil moisture at different depths, yield, CO2 and N2O emissions) is used to rigorously test the LandscapeDNDC biogeochemical model. The model is run in a Latin-hypercube-based uncertainty analysis framework to constrain model parameter uncertainty and derive behavioural model runs. The results indicate that the model is generally capable of predicting trace gas emissions, as evaluated with RMSE as the objective function. The model shows a reasonable performance in simulating the ecosystem C and N balances. The model-data fusion concept helps to detect remaining model errors, such as missing (e.g. freeze-thaw cycling) or incomplete model processes (e.g. respiration rates after harvest). This concept further elucidates the identification of missing model input sources (e.g. the uptake of N through shallow groundwater on grassland during the vegetation period) and uncertainty in the measured validation data (e.g. forest N2O emissions in winter months). Guidance is provided to improve the model structure and field measurements to further advance landscape-scale model predictions.

  8. Comprehensive effects of a sedge plant on CH4 and N2O emissions in an estuarine marsh

    NASA Astrophysics Data System (ADS)

    Li, Yangjie; Wang, Dongqi; Chen, Zhenlou; Hu, Hong

    2018-05-01

    Although there have been numerous studies focusing on plants' roles in methane (CH4) emissions, the influencing mechanism of wetland plants on nitrous oxide (N2O) emissions has rarely been studied. Here, we test whether wetland plants also play an important role in N2O emissions. Gas fluxes were determined using the in situ static flux chamber technique. We also carried out pore-water extractions, sedge removal experiments and tests of N2O transportation. The brackish marsh acted as a net source of both CH4 and N2O. However, sedge plants played the opposite role in CH4 and N2O emissions. The removal of the sedges led to reduced CH4 emissions and increased accumulation of CH4 inside the sediment. Apart from being a conduit for CH4 transport, the sedges made a greater contribution to CH4 oxidation than CH4 production. The sedges exerted inhibitory effects on the release of N2O. The N2O was barely detectable inside the sediment in both vegetated and vegetation-removed plots. The denitrification measurements and nitrogen addition (the addition rates were equal to 0.028, 0.056 and 0.112 g m-2) experiments suggest that denitrification associated with N2O production occurred mainly in the surface sediment layer. The vascular sedge could transport atmospheric N2O downward into the rhizosphere. The rhizospheric sediment, together with the vascular sedge, became an effective sink of atmospheric N2O.

  9. Seasonal variation in measured H2O and CO2 flux of irrigated rice in the Mid-South

    USDA-ARS?s Scientific Manuscript database

    Rice production in the Lower Mississippi River Basin constitutes over half of US rice production, but little research has been done on water and carbon flux in this region at the field scale. Eddy covariance measurements of water and CO2 flux allow for an integrated field measurement of the interac...

  10. Evaluation of a lower-powered analyzer and sampling system for eddy-covariance measurements of nitrous oxide fluxes

    NASA Astrophysics Data System (ADS)

    Brown, Shannon E.; Sargent, Steve; Wagner-Riddle, Claudia

    2018-03-01

    Nitrous oxide (N2O) fluxes measured using the eddy-covariance method capture the spatial and temporal heterogeneity of N2O emissions. Most closed-path trace-gas analyzers for eddy-covariance measurements have large-volume, multi-pass absorption cells that necessitate high flow rates for ample frequency response, thus requiring high-power sample pumps. Other sampling system components, including rain caps, filters, dryers, and tubing, can also degrade system frequency response. This field trial tested the performance of a closed-path eddy-covariance system for N2O flux measurements with improvements to use less power while maintaining the frequency response. The new system consists of a thermoelectrically cooled tunable diode laser absorption spectrometer configured to measure both N2O and carbon dioxide (CO2). The system features a relatively small, single-pass sample cell (200 mL) that provides good frequency response with a lower-powered pump ( ˜ 250 W). A new filterless intake removes particulates from the sample air stream with no additional mixing volume that could degrade frequency response. A single-tube dryer removes water vapour from the sample to avoid the need for density or spectroscopic corrections, while maintaining frequency response. This eddy-covariance system was collocated with a previous tunable diode laser absorption spectrometer model to compare N2O and CO2 flux measurements for two full growing seasons (May 2015 to October 2016) in a fertilized cornfield in Southern Ontario, Canada. Both spectrometers were placed outdoors at the base of the sampling tower, demonstrating ruggedness for a range of environmental conditions (minimum to maximum daily temperature range: -26.1 to 31.6 °C). The new system rarely required maintenance. An in situ frequency-response test demonstrated that the cutoff frequency of the new system was better than the old system (3.5 Hz compared to 2.30 Hz) and similar to that of a closed-path CO2 eddy-covariance system (4

  11. Effects of coastal marsh conversion to shrimp aquaculture ponds on CH4 and N2O emissions

    NASA Astrophysics Data System (ADS)

    Yang, P.; Bastviken, D.; Lai, D. Y. F.; Jin, B. S.; Mou, X. J.; Tong, C.; Yao, Y. C.

    2017-12-01

    In this study, we compared the CH4 and N2O fluxes from a tidal brackish Cyperus malaccensis marsh ecosystem and nearby shrimp ponds, converted from C. malaccensis marsh in the last 3-4 years, in the Min River estuary of southeast China over the aquaculture period of the year. Significant differences in CH4 and N2O fluxes were observed in space (between brackish marsh and shrimp ponds) and in time (between sampling occasions that were distributed over the aquaculture period). CH4 fluxes from the shrimp ponds were on an average 10-fold higher than from the brackish marsh. N2O emissions, on the other hand, were lower from the shrimp pond (25% of the emissions from the brackish marsh). Accessory data indicates that these patterns were primarily linked to water level variability and temperature (all fluxes), sediment porewater sulfate concentrations (CH4 flux) and total nitrogen concentrations (N2O flux). Our research demonstrates that the coastal marsh ecosystem converted to aquaculture ponds considerably alter emissions of CH4 and N2O and provides input to the global discussion on how to account for emissions from various types of flooded land in greenhouse gas inventories.

  12. Effects of warming on CO2, N2O and CH4 fluxes and underlying processes from subarctic tundra, Northwest Russia

    NASA Astrophysics Data System (ADS)

    Voigt, Carolina; Lamprecht, Richard E.; Marushchak, Maija E.; Biasi, Christina; Martikainen, Pertti J.

    2014-05-01

    Peatlands, especially those located in the highly sensitive arctic and subarctic latitudes, are known to play a major role in the global carbon cycle. Predicted climatic changes - entailing an increase in near-surface temperature and a change in precipitation patterns - will most likely have a serious yet uncertain impact on the greenhouse gas (GHG) balance of these ecosystems. Microbial processes are enhanced by warmer temperatures which may lead to increased trace gas fluxes to the atmosphere. However, the response of ecosystem processes and related GHG fluxes may differ largely across the landscape depending on soil type, vegetation cover, and moisture conditions. In this study we investigate how temperature increase potentially reflects on GHG fluxes (CO2, CH4 and N2O) from various tundra surfaces in the Russian Arctic. These surfaces include raised peat plateau complexes, mineral tundra soils, bare surfaces affected by frost action such as peat circles and thermokarst lake walls, as well as wetlands. Predicted temperature increase and climate change effects are simulated by means of open top chambers (OTCs), which are placed on different soil types for the whole snow-free period. GHG fluxes, gas and nutrient concentrations in the soil profile, as well as supporting environmental parameters are monitored for the full growing season. Aim of the study is not only the quantification of aboveground GHG fluxes from the study area, but the linking of those to underlying biogeochemical processes in permafrost soils. Special emphasis is placed on the interface between active layer and old permafrost and its response to warming, since little is known about the lability of old carbon stocks made available through an increase in active layer depth. Overall goal of the study is to gain a better understanding of C and N cycling in subarctic tundra soils and to deepen knowledge in respect to carbon-permafrost feedbacks in respect to climate.

  13. Flux growth of high-quality CoFe 2O 4 single crystals and their characterization

    NASA Astrophysics Data System (ADS)

    Wang, W. H.; Ren, X.

    2006-04-01

    We report the growth of high-quality CoFe 2O 4 single crystals using a borax flux method. The crystals were characterized by powder X-ray diffraction, electron probe microanalysis and Raman spectroscopy. We found the crystals are flux-free and highly homogeneous in composition. X-ray rocking curves of the CoFe 2O 4 single crystals showed a full-width at half-maximum of 0.15°. The saturation magnetization of the CoFe 2O 4 single crystals was measured to be 90 emu/g or equivalently 3.65 μ B/f.u. at 5 K.

  14. USDA-ARS GRACEnet Project Protocols, Chapter 3. Chamber-based trace gas flux measurements4

    USDA-ARS?s Scientific Manuscript database

    This protocol addresses N2O, CO2 and CH4 flux measurement by soil chamber methodology. The reactivities of other gasses of interest such as NOx O3, CO, and NH3 will require different chambers and associated instrumentation. Carbon dioxide is included as an analyte with this protocol; however, when p...

  15. Investigation of the N2O emission strength in the U. S. Corn Belt

    NASA Astrophysics Data System (ADS)

    Fu, Congsheng; Lee, Xuhui; Griffis, Timothy J.; Dlugokencky, Edward J.; Andrews, Arlyn E.

    2017-09-01

    Nitrous oxide (N2O) has a high global warming potential and depletes stratospheric ozone. The U. S. Corn Belt plays an important role in the global anthropogenic N2O budget. To date, studies on local surface N2O emissions and the atmospheric N2O budget have commonly used Lagrangian models. In the present study, we used an Eulerian model - Weather Research and Forecasting Chemistry (WRF-Chem) model to investigate the relationships between N2O emissions in the Corn Belt and observed atmospheric N2O mixing ratios. We derived a simple equation to relate the emission strengths to atmospheric N2O mixing ratios, and used the derived equation and hourly atmospheric N2O measurements at the KCMP tall tower in Minnesota to constrain agricultural N2O emissions. The modeled spatial patterns of atmospheric N2O were evaluated against discrete observations at multiple tall towers in the NOAA flask network. After optimization of the surface flux, the model reproduced reasonably well the hourly N2O mixing ratios monitored at the KCMP tower. Agricultural N2O emissions in the EDGAR42 database needed to be scaled up by 19.0 to 28.1 fold to represent the true emissions in the Corn Belt for June 1-20, 2010 - a peak emission period. Optimized mean N2O emissions were 3.00-4.38, 1.52-2.08, 0.61-0.81 and 0.56-0.75 nmol m- 2 s- 1 for June 1-20, August 1-20, October 1-20 and December 1-20, 2010, respectively. The simulated spatial patterns of atmospheric N2O mixing ratios after optimization were in good agreement with the NOAA discrete observations during the strong emission peak in June. Such spatial patterns suggest that the underestimate of emissions using IPCC (Inter-governmental Panel on Climate Change) inventory methodology is not dependent on tower measurement location.

  16. Effect of watershed urbanization on N2O emissions from the Chongqing metropolitan river network, China

    NASA Astrophysics Data System (ADS)

    He, Yixin; Wang, Xiaofeng; Chen, Huai; Yuan, Xingzhong; Wu, Ning; Zhang, Yuewei; Yue, Junsheng; Zhang, Qiaoyong; Diao, Yuanbin; Zhou, Lilei

    2017-12-01

    Watershed urbanization, an integrated anthropogenic perturbation, is another considerable global concern in addition to that of global warming and may significantly enrich the N loadings of watersheds, which then greatly influences the nitrous oxide (N2O) production and fluxes of these aquatic systems. However, little is known about the N2O dynamics in human-dominated metropolitan river networks. In this study, we present the temporal and spatial variations in N2O saturation and emission in the Chongqing metropolitan river network, which is undergoing intensified urbanization. The N2O saturation and fluxes at 84 sampling sites ranged from 126% to 10536% and from 4.5 to 1566.8 μmol N2O m-2 d-1, with means of 1780% and 261 μmol N2O m-2 d-1. The riverine N2O saturation and fluxes increased along with the urbanization gradient and urbanization rate, with disproportionately higher values in urban rivers due to the N2O-rich sewage inputs and enriched in situ N substrates. We found a clear seasonal pattern of N2O saturation, which was co-regulated by both water temperature and precipitation. Regression analysis indicated that the N substrates and dissolved oxygen (DO) that controlled nitrogen metabolism acted as good predictors of the N2O emissions of urban river networks. Particularly, phosphorus (P) and hydromorphological factors (water velocity, river size and bottom substrate) had stronger relationships with the N2O saturation and could also be used to predict the N2O emission hotspots in regions with rapid urbanization. In addition, the default emission factors (EF5-r) used in the Intergovernmental Panel on Climate Change (IPCC) methodology may need revision given the differences among the physical and chemical factors in different rivers, especially urban rivers.

  17. Comparison of methods for the determination of NO-O3-NO2 fluxes and chemical interactions over a bare soil

    NASA Astrophysics Data System (ADS)

    Stella, P.; Loubet, B.; Laville, P.; Lamaud, E.; Cazaunau, M.; Laufs, S.; Bernard, F.; Grosselin, B.; Mascher, N.; Kurtenbach, R.; Mellouki, A.; Kleffmann, J.; Cellier, P.

    2011-08-01

    Tropospheric ozone (O3) is a known greenhouse gas responsible for impacts on human and animal health and ecosystem functioning. In addition, O3 plays an important role in tropospheric chemistry, together with nitrogen oxides. Flux measurements of these trace gases are a major issue to establish their atmospheric budget and evaluate the ozone impact onto the biosphere. In this study, ozone, nitric oxide (NO) and nitrogen dioxide (NO2) fluxes were measured using the aerodynamic gradient method over a bare soil in an agricultural field. Vertical mixing ratio profile measurements were performed with fast response sensors. It was demonstrated that corrections of the aerodynamic gradient for chemical reactions between O3-NO-NO2 appeared to be negligible for O3 fluxes, whereas they accounted for about 10 % on average of the NO and NO2 fluxes. The flux uncertainties were mainly due to uncertainties of the friction velocity. In addition, the use of fast response sensors allowed to reduce the remaining part of the flux uncertainty. The aerodynamic gradient and eddy-covariance methods gave similar O3 fluxes (within 4 %). The chamber NO fluxes were up to 70 % lower than the aerodynamic gradient fluxes probably caused by either the spatial heterogeneity of the soil NO emissions or the environmental perturbation due to the chamber.

  18. Isotopic Monitoring of N2O Emissions from Wastewater Treatment: Evidence for N2O Production Associated with Anammox Metabolism?

    NASA Astrophysics Data System (ADS)

    Harris, E. J.; Wunderlin, P.; Joss, A.; Emmenegger, L.; Kipf, M.; Wolf, B.; Mohn, J.

    2015-12-01

    Microbial production is the major source of N2O, the strongest greenhouse gas produced within the nitrogen cycle, and the most important stratospheric ozone destructant released in the 21st century. Wastewater treatment is an important and growing source of N2O, with best estimates predicting N2O emissions from this sector will have increased by >25% by 2020. Novel treatment employing partial nitritation-anammox, rather than traditional nitrification-denitrification, has the potential to achieve a neutral carbon footprint due to increased biogas production - if N2O production accounts for <0.5-1% of total nitrogen turnover. As a further motivation for this research, microbial pathways identified from wastewater treatment can be applied to our understanding of N cycling in the natural environment. This study presents the first online isotopic measurements of offgas N2O from a partial-nitritation anammox reactor 1. The measured N2O isotopic composition - in particular the N2O isotopic site preference (SP = δ15Nα - δ15Nβ) - was used to understand N2O production pathways in the reactor. When N2O emissions peaked due to high dissolved oxygen concentrations, low SP showed that N2O was produced primarily via nitrifier denitrification by ammonia oxidizing bacteria (AOBs). N2O production by AOBs via NH2OH oxidation, in contrast, did not appear to be important under any conditions. Over the majority of the one-month measurement period, the measured SP was much higher than expected following our current understanding of N2O production pathways 2. SP reached 41‰ during normal operating conditions and achieved a maximum of 45‰ when nitrite was added under anoxic conditions. These results could be explained by unexpectedly strong heterotrophic N2O reduction despite low dissolved organic matter concentrations, or by an incomplete understanding of isotopic fractionation during N2O production from NH2OH oxidation by AOBs - however the explanation most consistent with all

  19. Quenching of I(2P1/2) by NO2, N2O4, and N2O.

    PubMed

    Kabir, Md Humayun; Azyazov, Valeriy N; Heaven, Michael C

    2007-10-11

    Quenching of excited iodine atoms (I(5p5, 2P1/2)) by nitrogen oxides are processes of relevance to discharge-driven oxygen iodine lasers. Rate constants at ambient and elevated temperatures (293-380 K) for quenching of I(2P1/2) atoms by NO2, N2O4, and N2O have been measured using time-resolved I(2P1/2) --> I(2P3/2) 1315 nm emission. The excited atoms were generated by pulsed laser photodissociation of CF3I at 248 nm. The rate constants for I(2P1/2) quenching by NO2 and N2O were found to be independent of temperature over the range examined with average values of (2.9 +/- 0.3) x 10(-15) and (1.4 +/- 0.1) x 10(-15) cm3 s(-1), respectively. The rate constant for quenching of I(2P1/2) by N2O4 was found to be (3.5 +/- 0.5) x 10(-13) cm3 s(-1) at ambient temperature.

  20. Flux flow induced microwave absorption in high temperature superconductor Bi 2-XPb XSr 2Ca N-1Cu NO 4+2N

    NASA Astrophysics Data System (ADS)

    Owens, F. J.

    1990-12-01

    Direct measurements of microwave absorption without use of rf H field modulation in granular composites of the 115 K superconductor Bi 2-XPb XSr 2Ca N-1Cu NO 4+2N as a function of magnetic field above 0.1 T reveal a continuing increase of absorption of microwave energy increasing magnetic field. The temperature and magnetic field dependence of the absorption are very different from the low magnetic field (<0.01 T) absorption arising from weak links in the material. The magnetic field and temperature dependence are consistent with the behavior of thermally activated flux flow resistance suggesting the absorption is due to flux creep.

  1. Relating N2O emissions during biological nitrogen removal with operating conditions using multivariate statistical techniques.

    PubMed

    Vasilaki, V; Volcke, E I P; Nandi, A K; van Loosdrecht, M C M; Katsou, E

    2018-04-26

    Multivariate statistical analysis was applied to investigate the dependencies and underlying patterns between N 2 O emissions and online operational variables (dissolved oxygen and nitrogen component concentrations, temperature and influent flow-rate) during biological nitrogen removal from wastewater. The system under study was a full-scale reactor, for which hourly sensor data were available. The 15-month long monitoring campaign was divided into 10 sub-periods based on the profile of N 2 O emissions, using Binary Segmentation. The dependencies between operating variables and N 2 O emissions fluctuated according to Spearman's rank correlation. The correlation between N 2 O emissions and nitrite concentrations ranged between 0.51 and 0.78. Correlation >0.7 between N 2 O emissions and nitrate concentrations was observed at sub-periods with average temperature lower than 12 °C. Hierarchical k-means clustering and principal component analysis linked N 2 O emission peaks with precipitation events and ammonium concentrations higher than 2 mg/L, especially in sub-periods characterized by low N 2 O fluxes. Additionally, the highest ranges of measured N 2 O fluxes belonged to clusters corresponding with NO 3 -N concentration less than 1 mg/L in the upstream plug-flow reactor (middle of oxic zone), indicating slow nitrification rates. The results showed that the range of N 2 O emissions partially depends on the prior behavior of the system. The principal component analysis validated the findings from the clustering analysis and showed that ammonium, nitrate, nitrite and temperature explained a considerable percentage of the variance in the system for the majority of the sub-periods. The applied statistical methods, linked the different ranges of emissions with the system variables, provided insights on the effect of operating conditions on N 2 O emissions in each sub-period and can be integrated into N 2 O emissions data processing at wastewater treatment plants

  2. Carbon Dioxide and Water Vapor Concentrations, Co-spectra and Fluxes from Latest Standardized Automated CO2/H2O Flux Systems versus Established Analyzer Models

    NASA Astrophysics Data System (ADS)

    Burba, G. G.; Kathilankal, J. C.; Begashaw, I.; Franzen, D.; Welles, J.; McDermitt, D. K.

    2017-12-01

    Spatial and temporal flux data coverage have improved significantly in recent years, due to standardization, automation and management of data collection, and better handling of the generated data. With more stations and networks, larger data streams from each station, and smaller operating budgets, modern tools are required to effectively and efficiently handle the entire process.These tools should produce standardized verifiable datasets, and provide a way to cross-share the standardized data with external collaborators to leverage available funding, and promote data analyses and publications. In 2015, new open-path and enclosed flux measurement systems1 were developed, based on established gas analyzer models2,3, with the goal of improving stability in the presence of contamination, refining temperature control and compensation, and providing more accurate gas concentration measurements. In 2017, the new open-path system was further refined to simplify hardware configuration, and to reduce power consumption and cost. Additionally, all new systems incorporate complete automated on-site flux calculations using EddyPro® Software4 run by a weatherized remotely-accessible microcomputer to provide standardized traceable data sets for fluxes and supporting variables. This presentation will describe details and results from the field tests of the new flux systems, in comparison to older models and reference instruments. References:1 Burba G., W. Miller, I. Begashaw, G. Fratini, F. Griessbaum, J. Kathilankal, L. Xu, D. Franz, E. Joseph, E. Larmanou, S. Miller, D. Papale, S. Sabbatini, T. Sachs, R. Sakai, D. McDermitt, 2017. Comparison of CO2 Concentrations, Co-spectra and Flux Measurements between Latest Standardized Automated CO2/H2O Flux Systems and Older Gas Analysers. 10th ICDC Conference, Switzerland: 21-25/08 2 Metzger, S., G. Burba, S. Burns, P. Blanken, J. Li, H. Luo, R. Zulueta, 2016. Optimization of an enclosed gas analyzer sampling system for measuring eddy

  3. Spatial and temporal variability of N2O emission on grazed pastures - influence of management and meteorological drivers

    NASA Astrophysics Data System (ADS)

    Ammann, Christof; Voglmeier, Karl; Jocher, Markus

    2017-04-01

    Grazed pastures are considered as strong sources of the greenhouse gas nitrous oxide (N2O) with local hot-spots resulting from the uneven spatial distribution of the excretion of the grazing animals. Especially urine patches can result in a high local nitrogen (N) surplus, which can cause large deviations from average soil conditions. The strong spatial and temporal variability of the gaseous emissions represents an inherent problem for the quantification, interpretation and modelling. Micrometeorological methods integrating over a larger domain like the eddy covariance method are well suited to quantify the integrated ecosystem emissions of N2O. In contrast, chamber methods are more useful to investigate specific underlying processes and their dependences on driving parameters. We present results of a pasture experiment in western Switzerland where eddy covariance and chamber measurements of N2O fluxes have been performed using a very sensitive and fast response quantum cascade laser (QCL) instrument. Small scale emissions of N2O from dung and urine patches as well as from other "background" pasture surface areas were quantified using an optimized 'fast-box' chamber system. Variable and partly high N2O emissions of the pasture were observed during all seasons. Beside management factors (grazing phases, fertiliser application), temperature and soil moisture showed a large effect on the fluxes. Fresh urine patches from grazing cows were found to be main emission sources and their temporal dynamics was studied in detail. We present a first approach to up-scale the chamber measurements to the field-scale and compare the results with the eddy covariance measurements.

  4. Biochar effects on gaseous losses of N2O and CH4

    USDA-ARS?s Scientific Manuscript database

    The flux of N2O from soil is controlled by both biological and abiotic processes resulting in production and consumption. In a recent review by Butterbach-Bahl et al., (2013), key processes that contribute to N2O formation in soils included: 1) chemical decomposition of hydroxylamine during autotrop...

  5. Improving estimates of N2O emissions for western and central Europe using a Bayesian inversion approach

    NASA Astrophysics Data System (ADS)

    Thompson, R. L.; Gerbig, C.; Roedenbeck, C.; Heimann, M.

    2009-04-01

    The nitrous oxide (N2O) mixing ratio has been increasing in the atmosphere since the industrial revolution, from 270 ppb in 1750 to 320 ppb in 2007 with a steady growth rate of around 0.26% since the early 1980's. The increase in N2O is worrisome for two main reasons. First, it is a greenhouse gas; this means that its atmospheric increase translates to an enhancement in radiative forcing of 0.16 ± 0.02 Wm-2 making it currently the fourth most important long-lived greenhouse gas and is predicted to soon overtake CFC's to become the third most important. Second, it plays an important role in stratospheric ozone chemistry. Human activities are the primary cause of the atmospheric N2O increase. The largest anthropogenic source of N2O is from the use of N-fertilizers in agriculture but fossil fuel combustion and industrial processes, such as adipic and nitric acid production, are also important. We present a Bayesian inversion approach for estimating N2O fluxes over central and western Europe using high frequency in-situ concentration data from the Ochsenkopf tall tower (50 °01′N, 11 °48′, 1022 masl). For the inversion, we employ a Lagrangian-type transport model, STILT, which provides source-receptor relationships at 10 km using ECMWF meteorological data. The a priori flux estimates used were from IER, for anthropogenic, and GEIA, for natural fluxes. N2O fluxes were retrieved monthly at 2 x 2 degree spatial resolution for 2007. The retrieved N2O fluxes showed significantly more spatial heterogeneity than in the a priori field and considerable seasonal variability. The timing of peak emissions was different for different regions but in general the months with the strongest emissions were May and August. Overall, the retrieved flux (anthropogenic and natural) was lower than in the a priori field.

  6. Eddy covariance fluxes of the NO-NO2-O3 triad above a spruce forest canopy in south-eastern Germany.

    NASA Astrophysics Data System (ADS)

    Tsokankunku, A.; Zhu, Z.; Meixner, F. X.; Foken, T.; Andreae, M. O.

    2009-04-01

    We investigated the diel variability of the eddy covariance fluxes of the NO-NO2-O3 triad above a spruce forest canopy at the "Weidenbrunnen" research site (Fichtelgebirge, Germany). Measurements were part of the EGER project (ExchanGE processes in mountainous Regions), which focuses on the role of process interactions among the different scales of soil, in-canopy and atmospheric exchange processes of reactive and non-reactive trace gases and energy. The eddy covariance platform was at the top of a 32 m high tower (50˚ 08'31" N, 11˚ 52'1"E, elevation 755 m.a.s.l). The eddy covariance system consisted of a CSAT3 sonic anemometer and a high speed, high resolution NO-NO2two channel chemiluminescence analyzer (Ecophysics CLD 790 SR2). A solid-state blue-light photolytic converter was connected to the NO2 channel of the analyzer just behind the sample inlet. Ambient NO and NO2 mixing ratios were sampled via 52 m long tubes with the instrument itself located in a temperature-controlled container at the ground. The NO-NO2 analyzer was operated at 5 Hz. Additionally we measured eddy covariance fluxes of CO2 and H2O. An infrared absorption-based analyzer (LI-7000) was used to sample CO2 and H2O mixing ratios, and a fast solid-phase chemiluminescence ozone analyzer (GFAS) was deployed to measure O3 mixing ratios. All trace gas inlets were situated at 32.5 m, 20 cm below the path of the sonic anemometer. The 32m inlet of an independent NO, NO2, and O3 concentration profile measuring system was used as the calibration source for the fast ozone analyzer and the two channel NO-NO2chemiluminescence analyzer. Preliminary results show that NO and NO2advection plays a big role in the magnitude and direction of the fluxes at the site. The main source of the advection is a busy country road situated about 2 km west of the site. CO2 fluxes were also influenced by advection. Extended periods of stationarity usually occurred on Sundays when the amount of traffic was significantly

  7. Diel and seasonal nitrous oxide fluxes determined by floating chamber and gas transfer equation methods in agricultural irrigation watersheds in southeast China.

    PubMed

    Wu, Shuang; Chen, Jie; Li, Chen; Kong, Delei; Yu, Kai; Liu, Shuwei; Zou, Jianwen

    2018-02-07

    Agricultural nitrate leaching and runoff incurs high nitrogen loads in agricultural irrigation watersheds, constituting one of important sources of atmospheric nitrous oxide (N 2 O). Two independent sampling campaigns of N 2 O flux measurement over diel cycles and N 2 O flux measurements once a week over annual cycles were carried out in an agricultural irrigation watershed in southeast China using floating chamber (chamber-based) and gas transfer equation (model-based) methods. The diel and seasonal patterns of N 2 O fluxes did not differ between the two measurement methods. The diel variation in N 2 O fluxes was characterized by the pattern that N 2 O fluxes were greater during nighttime than daytime periods with a single flux peak at midnight. The diel variation in N 2 O fluxes was closely associated with water environment and chemistry. The time interval of 9:00-11:00 a.m. was identified to be the sampling time best representing daily N 2 O flux measurements in agricultural irrigation watersheds. Seasonal N 2 O fluxes showed large variation, with some flux peaks corresponding to agricultural irrigation and drainage episodes and heavy rainfall during the crop-growing period of May to November. On average, N 2 O fluxes calculated by model-based methods were 27% lower than those determined by the chamber-based techniques over diel or annual cycles. Overall, more measurement campaigns are highly needed to assess regional agricultural N 2 O budget with low uncertainties.

  8. Method for measuring changes in the atmospheric O2/N2 ratio by a gas chromatograph equipped with a thermal conductivity detector

    NASA Astrophysics Data System (ADS)

    Tohjima, Yasunori

    2000-06-01

    We present a method for measuring changes in the atmospheric O2/N2 ratio based on data from a gas chromatograph (GC) equipped with a thermal conductivity detector (TCD). In this method, O2 and N2 in an air sample are separated on a column filled with molecular sieve 5A with H2 carrier gas. Since the separated O2 includes Ar, which has a retention time similar to that of O2, the (O2+Ar)/N2 ratio is actually measured. The change in the measured (O2+Ar)/N2 ratio can be easily converted to that in the O2/N2 ratio with a very small error based on the fact that the atmospheric Ar/N2 ratio is almost constant. The improvements to achieve the high-precision measurement include stabilization of the pressure at the GC column head and at the outlets of the TCD and the sample loop. Additionally, the precision is improved statistically by repeating alternate analyses of sample and a reference gas. The standard deviation of the replicate cycles of reference and sample analyses is about 18 per meg (corresponding to 3.8 parts per million (ppm) O2 in air). This means that the standard error is about 7 per meg (1.5 ppm O2 in air) for seven cycles of alternate analyses, which takes about 70 min. The response of this method is likely to have a 2% nonlinearity. Ambient air samples are collected under pressure in glass flasks equipped with two stopcocks sealed by Viton O-rings at both ends. Pressure depletion in the flask during the O2/N2 measurement does not cause any detectable change in the O2/N2 ratio, but the O2/N2 ratio in the flask was found to gradually decrease during the storage period. We also present preliminary results from air samples collected at Hateruma Island (latitude 24°03'N, longitude 123°49') from July 1997 through March 1999. The observed O2/N2 ratios clearly show a seasonal variation, increasing in spring and summer and decreasing in autumn and winter.

  9. Permafrost collapse shifts alpine tundra to a carbon source but reduces N2O and CH4 release on the northern Qinghai-Tibetan Plateau

    NASA Astrophysics Data System (ADS)

    Mu, C. C.; Abbott, B. W.; Zhao, Q.; Su, H.; Wang, S. F.; Wu, Q. B.; Zhang, T. J.; Wu, X. D.

    2017-09-01

    Important unknowns remain about how abrupt permafrost collapse (thermokarst) affects carbon balance and greenhouse gas flux, limiting our ability to predict the magnitude and timing of the permafrost carbon feedback. We measured monthly, growing-season fluxes of CO2, CH4, and N2O at a large thermokarst feature in alpine tundra on the northern Qinghai-Tibetan Plateau (QTP). Thermokarst formation disrupted plant growth and soil hydrology, shifting the ecosystem from a growing-season carbon sink to a weak source but decreasing feature level CH4 and N2O flux. Temperature-corrected ecosystem respiration from decomposing permafrost soil was 2.7 to 9.5-fold higher than in similar features from Arctic and Boreal regions, suggesting that warmer and dryer conditions on the northern QTP could accelerate carbon decomposition following permafrost collapse. N2O flux was similar to the highest values reported for Arctic ecosystems and was 60% higher from exposed mineral soil on the feature floor, confirming Arctic observations of coupled nitrification and denitrification in collapsed soils. Q10 values for respiration were typically over 4, suggesting high-temperature sensitivity of thawed carbon. Taken together, these results suggest that QTP permafrost carbon in alpine tundra is highly vulnerable to mineralization following thaw, and that N2O production could be an important noncarbon permafrost climate feedback. Permafrost collapse altered soil hydrology, shifting the ecosystem from a carbon sink to carbon source but decreasing CH4 and N2O flux. Little to no vegetation recovery after stabilization suggests potentially large net carbon losses. High N2O flux compared to Arctic and Boreal systems suggests noncarbon permafrost climate feedback.

  10. Comparison of two closed-path cavity-based spectrometers for measuring air-water CO2 and CH4 fluxes by eddy covariance

    NASA Astrophysics Data System (ADS)

    Yang, Mingxi; Prytherch, John; Kozlova, Elena; Yelland, Margaret J.; Parenkat Mony, Deepulal; Bell, Thomas G.

    2016-11-01

    In recent years several commercialised closed-path cavity-based spectroscopic instruments designed for eddy covariance flux measurements of carbon dioxide (CO2), methane (CH4), and water vapour (H2O) have become available. Here we compare the performance of two leading models - the Picarro G2311-f and the Los Gatos Research (LGR) Fast Greenhouse Gas Analyzer (FGGA) at a coastal site. Both instruments can compute dry mixing ratios of CO2 and CH4 based on concurrently measured H2O, temperature, and pressure. Additionally, we used a high throughput Nafion dryer to physically remove H2O from the Picarro airstream. Observed air-sea CO2 and CH4 fluxes from these two analysers, averaging about 12 and 0.12 mmol m-2 day-1 respectively, agree within the measurement uncertainties. For the purpose of quantifying dry CO2 and CH4 fluxes downstream of a long inlet, the numerical H2O corrections appear to be reasonably effective and lead to results that are comparable to physical removal of H2O with a Nafion dryer in the mean. We estimate the high-frequency attenuation of fluxes in our closed-path set-up, which was relatively small ( ≤ 10 %) for CO2 and CH4 but very large for the more polar H2O. The Picarro showed significantly lower noise and flux detection limits than the LGR. The hourly flux detection limit for the Picarro was about 2 mmol m-2 day-1 for CO2 and 0.02 mmol m-2 day-1 for CH4. For the LGR these detection limits were about 8 and 0.05 mmol m-2 day-1. Using global maps of monthly mean air-sea CO2 flux as reference, we estimate that the Picarro and LGR can resolve hourly CO2 fluxes from roughly 40 and 4 % of the world's oceans respectively. Averaging over longer timescales would be required in regions with smaller fluxes. Hourly flux detection limits of CH4 from both instruments are generally higher than the expected emissions from the open ocean, though the signal to noise of this measurement may improve closer to the coast.

  11. A Reaction Between High Mn-High Al Steel and CaO-SiO2-Type Molten Mold Flux: Part I. Composition Evolution in Molten Mold Flux

    NASA Astrophysics Data System (ADS)

    Kim, Min-Su; Lee, Su-Wan; Cho, Jung-Wook; Park, Min-Seok; Lee, Hae-Geon; Kang, Youn-Bae

    2013-04-01

    In order to elucidate the reaction mechanism between high Mn-high Al steel such as twin-induced plasticity steel and molten mold flux composed mainly of CaO-SiO2 during continuous casting process, a series of laboratory-scale experiments were carried out in the present study. Molten steel and molten flux were brought to react in a refractory crucible in a temperature range between 1713 K to 1823 K (1440 °C to 1550 °C) and composition evolution in the steel and the flux was analyzed using inductively coupled plasma atomic emission spectroscopy, X-ray fluorescence, and electron probe microanalysis. The amount of SiO2 in the flux was significantly reduced by Al in the steel; thus, Al2O3 was accumulated in the flux as a result of a chemical reaction, 4[Al] + 3(SiO2) = 3[Si] + 2(Al2O3). In order to find a major factor which governs the reaction, a number of factors ((pct CaO/pct SiO2), (pct Al2O3), [pct Al], [pct Si], and temperature) were varied in the experiments. It was found that the above chemical reaction was mostly governed by [pct Al] in the molten steel. Temperature had a mild effect on the reaction. On the other hand, (pct CaO/pct SiO2), (pct Al2O3), and [pct Si] did not show any noticeable effect on the reaction. Apart from the above reaction, the following reactions are also thought to happen simultaneously: 2[Mn] + (SiO2) = [Si] + 2(MnO) and 2[Fe] + (SiO2) = [Si] + 2(FeO). These oxide components were subsequently reduced by Al in the molten steel. Na2O in the molten flux was gradually decreased and the decrease was accelerated by increasing [pct Al] and temperature. Possible reactions affecting the Al2O3 accumulation are summarized.

  12. Measurements of N2O and SF6 for use in Inverse Model Studies

    NASA Astrophysics Data System (ADS)

    Dlugokencky, E. J.; Peters, W.; Masarie, K. A.; Lang, P. M.; Dutton, G.; Hall, B. D.

    2004-12-01

    NOAA CMDL makes measurements of atmospheric nitrous oxide (N2O) and sulfur hexafluoride (SF6) mole fractions in discrete air samples from ˜60 surface sites and ˜10 vertical profile sites for use in inverse modeling. Measurements are made by gas chromatography with electron capture detection (ECD) relative to standard scales developed in CMDL's Halocarbons and Other Atmospheric Trace Species (HATS) group. Uncertainties in the standard scales (95% confidence limits) are 0.8 nmol mol-1 for N2O and 0.05 pmol mol-1 for SF6. For N2O, the ECD response is characterized monthly by a second-order polynomial with a suite of 6 secondary standards covering the range 242-343 nmol mol-1. An instrument response function prepared from measurements of the secondary standards relative to a reference cylinder is used to quantify samples. SF6 in air samples is quantified with the reference by assuming a linear response with zero intercept in samples that are free of SF6. Reproducibility of the measurements, based on agreement between two samples collected in series, is ˜0.4 nmol mol-1 for N2O and ˜0.04 pmol mol-1 for SF6. So far, all measurements have been made on a single analytical system. The measurements impose important constraints on the budgets of N2O and SF6 based on observed trends, changes in trends, and spatial gradients. These parameters can be used to determine source/sink imbalances, changes in emission rates over time, and the distribution of emissions. In addition, Peters et al. [JGR, in press, 2004] have used the SF6 measurements to evaluate transport in the two-way nested chemistry transport model, TM5. They found that TM5 captures vertical gradients and synoptic variability in SF6 well at both MBL and continental sampling sites, but it over-estimates the meridional gradient by ˜19%. The SF6 data also suggest that global SF6 emissions increased by ˜20% during late-2002.

  13. A Preliminary Study of CO2 Flux Measurements by Lidar

    NASA Technical Reports Server (NTRS)

    Gibert, Fabien; Koch, Grady J.; Beyon, Jeffrey Y.; Hilton, T.; Davis, Kenneth J.; Andrews, Arlyn; Ismail, Syed; Singh, Upendra N.

    2008-01-01

    A mechanistic understanding of the global carbon cycle requires quantification of terrestrial ecosystem CO2 fluxes at regional scales. In this paper, we analyze the potential of a Doppler DIAL system to make flux measurements of atmospheric CO2 using the eddy-covariance and boundary layer budget methods and present results from a ground based experiment. The goal of this study is to put CO2 flux point measurements in a mesoscale context. In June 2007, a field experiment combining a 2-m Doppler Heterodyne Differential Absorption Lidar (HDIAL) and in-situ sensors of a 447-m tall tower (WLEF) took place in Wisconsin. The HDIAL measures simultaneously: 1) CO2 mixing ratio, 2) atmosphere structure via aerosol backscatter and 3) radial velocity. We demonstrate how to synthesize these data into regional flux estimates. Lidar-inferred fluxes are compared with eddy-covariance fluxes obtained in-situ at 396m AGL from the tower. In cases where the lidar was not yet able to measure the fluxes with acceptable precision, we discuss possible modifications to improve system performance.

  14. Isotopomeric characterization of N2O produced, consumed, and emitted by automobiles.

    PubMed

    Toyoda, Sakae; Yamamoto, Sei-ichiro; Arai, Shinji; Nara, Hideki; Yoshida, Naohiro; Kashiwakura, Kiriko; Akiyama, Ken-ichi

    2008-01-01

    Fossil fuel combustion is the second largest anthropogenic source of nitrous oxide (N2O) after agriculture. The estimated global N2O flux from combustion sources, as well as from other sources, still has a large uncertainty. Herein, we characterize automobile sources using N2O isotopomer ratios (nitrogen and oxygen isotope ratios and intramolecular site preference of 15N, SP) to assess their contributions to total global sources and to deconvolute complex production/consumption processes during combustion and subsequent catalytic treatments of exhaust. Car exhaust gases were sampled under running and idling state, and N2O isotopomer ratios were measured by mass spectrometry. The N2O directly emitted from an engine of a vehicle running at constant velocity had almost constant isotopomer ratios (delta15Nbulk = -28.7 +/- 1.2 per thousand, delta18O = 28.6 +/- 3.3 per thousand, and SP = 4.2 +/- 0.8 per thousand) irrespective of the velocity. After passing through catalytic converters, the isotopomer ratios showed an increase which varied with the temperature and the aging of the catalysts. The increase suggests that both production and consumption of N2O occur on the catalyst and that their rates can be comparable. It was noticed that in the idling state, the N2O emitted from a brand new car has higher isotopomer ratios than that from used cars, which indicate that technical improvements in catalytic converters can reduce the N2O from mobile combustion sources. On average, the isotopomeric signatures of N2O finally emitted from automobiles are not sensitive to running/idling states or to aging of the catalysts. Characteristic average isotopomer ratios of N2O from automobile sources are estimated at -4.9 +/- 8.2 per thousand, 43.5 +/- 13.9 per thousand, and 12.2 +/- 9.1 per thousand for delta15Nbulk, delta18O, and SP, respectively.

  15. Two years monitoring of soil N_{2}O emissions on durum wheat in a Mediterranean area: the effect of tillage intensity and N-fertilizer rate.

    NASA Astrophysics Data System (ADS)

    Volpi, Iride; Bosco, Simona; Triana, Federico; Di Nasso, Nicoletta Nassi o.; Laville, Patricia; Virgili, Giorgio; Bonari, Enrico

    2016-04-01

    Evaluating the magnitude and the key factors affecting N2O emissions from agriculture has a scientific and practical relevance, in fact emissions from agricultural and natural soils account for 56-70% of all global N2O sources (Syakila and Kroeze, 2011). Moreover, the necessity to increase the food production rate minimizing greenhouse gas emissions require a deeper understanding of the effect of the agricultural practices on direct soil emissions. Therefore, the aim of this work is to assess the effect of tillage intensity and nitrogen rate on soil N2O emissions on durum wheat. A two years monitoring campaign was carried out using a high-sensibility transportable instrument developed within the LIFE+ "Improved flux Prototypes for N2O emission from Agriculture" IPNOA project (Bosco et al., 2015; Laville et al., 2015). The project aims at improving the measurement technique of N2O flux directly in field using the flow-through non-steady state chamber technique. The monitoring campaign on durum wheat lasted for two growing seasons and two fallow periods (2013-14 and 2014-15). Treatment on the main plot was tillage intensity with two levels, ploughing and minimum tillage, and three different nitrogen rates were distributed to the subplots (N0: 0 kg ha-1, N1: 110 kg ha-1, N2: 170 kg ha-1). Ancillary measurements concerned meteorological data, soil temperature and moisture, NO3-, NH4+ soil concentration. Main results of the two years highlighted N rate as the main driver for both N2O daily flux and cumulative emissions during the growing season, while in the fallow period treatments did not affect the emission magnitude. Tillage intensity was not a key factor for N2O emissions. N2O emissions were significantly different in the two years. In particular, cumulative emissions of 2013-14 were about five times higher than in 2014-15, respectively on average 2885±260 g N-N2O ha-1 and 534±53 g N-N2O ha-1 for a similar monitoring period of about 300 days. Differences could be

  16. Quantifying denitrification losses from a sub-tropical pasture in Queensland/Australia - use of the 15N gas flux method

    NASA Astrophysics Data System (ADS)

    Friedl, Johannes; Scheer, Clemens; Warner, Daniel; Grace, Peter

    2014-05-01

    The microbial mediated production of nitrous oxide (N2O) and its reduction to dinitrogen (N2) via denitrification represents a loss of nitrogen (N) from fertilised agro ecosystems to the atmosphere. Although denitrification remains a major uncertainty in estimating N losses from soils, the magnitude of N2 losses and related N2:N2O ratios from soils are largely unknown due to difficulties measuring N2 against a high atmospheric background. In order to address this lack of data, this study investigated the influence of different soil moisture contents on N2 and N2O emissions from a sub-tropical pasture in Queensland/Australia using the 15N gas flux method. Intact soil cores were incubated over 14 days at 80% and 100% water filled pore space (WFPS). Gas samples were taken up to six times per day after application of 15N labelled nitrate, equivalent to 50 kg N ha-1 and analysed for N2 and N2O by isotope ratio mass spectrometry. Fluxes were calculated assuming non-random 15N distribution in the headspace according to Mulvaney and Kurtz (1984) using the labelled pool of nitrate estimated from N2O measurements (Stevens and Laughlin 2001). The main product of denitrification in both treatments was N2. N2 emissions exceeded N2O emissions by a factor of 1.3 ± 0.3 at 80% WFPS and a factor of 3 ± 0.8 at 100% WFPS. The total amount of N-N2 lost over the incubation period was 13.5±1.0 kg N ha-1 at 80% WFPS and 21.8±1.8 kg ha-1 at 100% WFPS respectively. Over the entire incubation period, N2 emissions remained elevated at 100% WFPS, showing high variation between soil cores, while related N2O emissions decreased. At 80% WFPS, N2 emissions increased constantly over time showing significantly higher values after day five. At the same time, N2O fluxes declined. Consequently, N2:N2O ratios rose over the incubation period in both treatments. Overall denitrification rates and related N2:N2O ratios were higher at 100% WFPS compared to 80% WFPS, confirming WFPS as a major driver of

  17. Wet-season spatial variability of N2O emissions from a tea field in subtropical central China

    NASA Astrophysics Data System (ADS)

    Fu, X.; Liu, X.; Li, Y.; Shen, J.; Wang, Y.; Zou, G.; Li, H.; Song, L.; Wu, J.

    2015-01-01

    Tea fields emit large amounts of nitrous oxide (N2O) to the atmosphere. Obtaining accurate estimations of N2O emissions from tea-planted soils is challenging due to strong spatial variability. We examined the spatial variability of N2O emissions from a red-soil tea field in Hunan province, China, on 22 April 2012 (in a wet season) using 147 static mini chambers approximately regular gridded in a 4.0 ha tea field. The N2O fluxes for a 30 min snapshot (10-10.30 a.m.) ranged from -1.73 to 1659.11 g N ha-1 d-1 and were positively skewed with an average flux of 102.24 g N ha-1 d-1. The N2O flux data were transformed to a normal distribution by using a logit function. The geostatistical analyses of our data indicated that the logit-transformed N2O fluxes (FLUX30t) exhibited strong spatial autocorrelation, which was characterized by an exponential semivariogram model with an effective range of 25.2 m. As observed in the wet season, the logit-transformed soil ammonium-N (NH4Nt), soil nitrate-N (NO3Nt), soil organic carbon (SOCt), total soil nitrogen (TSNt) were all found to be significantly correlated with FLUX30t (r=0.57-0.71, p<0.001). Three spatial interpolation methods (ordinary kriging, regression kriging and cokriging) were applied to estimate the spatial distribution of N2O emissions over the study area. Cokriging with NH4Nt and NO3Nt as covariables (r= 0.74 and RMSE =1.18) outperformed ordinary kriging (r= 0.18 and RMSE =1.74), regression kriging with the sample position as a predictor (r= 0.49 and RMSE =1.55) and cokriging with SOCt as a covariable (r= 0.58 and RMSE =1.44). The predictions of the three kriging interpolation methods for the total N2O emissions of the 4.0 ha tea field ranged from 148.2 to 208.1 g N d-1, based on the 30 min snapshots obtained during the wet season. Our findings suggested that to accurately estimate the total N2O emissions over a region, the environmental variables (e.g., soil properties) and the current land use pattern (e.g., tea

  18. Wet-season spatial variability in N2O emissions from a tea field in subtropical central China

    NASA Astrophysics Data System (ADS)

    Fu, X.; Liu, X.; Li, Y.; Shen, J.; Wang, Y.; Zou, G.; Li, H.; Song, L.; Wu, J.

    2015-06-01

    Tea fields emit large amounts of nitrous oxide (N2O) to the atmosphere. Obtaining accurate estimations of N2O emissions from tea-planted soils is challenging due to strong spatial variability. We examined the spatial variability in N2O emissions from a red-soil tea field in Hunan Province, China, on 22 April 2012 (in a wet season) using 147 static mini chambers approximately regular gridded in a 4.0 ha tea field. The N2O fluxes for a 30 min snapshot (10:00-10:30 a.m.) ranged from -1.73 to 1659.11 g N ha-1 d-1 and were positively skewed with an average flux of 102.24 g N ha-1 d-1. The N2O flux data were transformed to a normal distribution by using a logit function. The geostatistical analyses of our data indicated that the logit-transformed N2O fluxes (FLUX30t) exhibited strong spatial autocorrelation, which was characterized by an exponential semivariogram model with an effective range of 25.2 m. As observed in the wet season, the logit-transformed soil ammonium-N (NH4Nt), soil nitrate-N (NO3Nt), soil organic carbon (SOCt) and total soil nitrogen (TSNt) were all found to be significantly correlated with FLUX30t (r = 0.57-0.71, p < 0.001). Three spatial interpolation methods (ordinary kriging, regression kriging and cokriging) were applied to estimate the spatial distribution of N2O emissions over the study area. Cokriging with NH4Nt and NO3Nt as covariables (r = 0.74 and RMSE = 1.18) outperformed ordinary kriging (r = 0.18 and RMSE = 1.74), regression kriging with the sample position as a predictor (r = 0.49 and RMSE = 1.55) and cokriging with SOCt as a covariable (r = 0.58 and RMSE = 1.44). The predictions of the three kriging interpolation methods for the total N2O emissions of 4.0 ha tea field ranged from 148.2 to 208.1 g N d-1, based on the 30 min snapshots obtained during the wet season. Our findings suggested that to accurately estimate the total N2O emissions over a region, the environmental variables (e.g., soil properties) and the current land use pattern

  19. An original experiment to determine impact of catch crop introduction in a crop rotation on N2O production fate

    NASA Astrophysics Data System (ADS)

    Tallec, Tiphaine; Le Dantec, Valérie; Zawilski, Bartosz; Brut, Aurore; Boussac, Marion; Ferlicoq, Morgan; Ceschia, Eric

    2015-04-01

    equipped to measure environmental parameters and N2O fluxes. Nitrous oxide fluxes were measured using six stainless steel automatic chambers coupled with an infra red gas analyzer every 6 hours. We first analyzed N2O flux rates obtained between the two treatments and then we quantified the impact of temperature and soil moisture on their daily and seasonal variations.

  20. Decreased N2O reduction by low soil pH causes high N2O emissions in a riparian ecosystem.

    PubMed

    Van den Heuvel, R N; Bakker, S E; Jetten, M S M; Hefting, M M

    2011-05-01

    Quantification of harmful nitrous oxide (N(2)O) emissions from soils is essential for mitigation measures. An important N(2)O producing and reducing process in soils is denitrification, which shows deceased rates at low pH. No clear relationship between N(2)O emissions and soil pH has yet been established because also the relative contribution of N(2)O as the denitrification end product decreases with pH. Our aim was to show the net effect of soil pH on N(2)O production and emission. Therefore, experiments were designed to investigate the effects of pH on NO(3)(-) reduction, N(2)O production and reduction and N(2) production in incubations with pH values set between 4 and 7. Furthermore, field measurements of soil pH and N(2)O emissions were carried out. In incubations, NO(3)(-) reduction and N(2) production rates increased with pH and net N(2)O production rate was highest at pH 5. N(2)O reduction to N(2) was halted until NO(3)(-) was depleted at low pH values, resulting in a built up of N(2)O. As a consequence, N(2)O:N(2) production ratio decreased exponentially with pH. N(2)O reduction appeared therefore more important than N(2)O production in explaining net N(2)O production rates. In the field, a negative exponential relationship for soil pH against N(2)O emissions was observed. Soil pH could therefore be used as a predictive tool for average N(2)O emissions in the studied ecosystem. The occurrence of low pH spots may explain N(2)O emission hotspot occurrence. Future studies should focus on the mechanism behind small scale soil pH variability and the effect of manipulating the pH of soils. © 2011 Blackwell Publishing Ltd.

  1. A meta-analysis of fertilizer-induced soil NO and combined NO+N2 O emissions.

    PubMed

    Liu, Shuwei; Lin, Feng; Wu, Shuang; Ji, Cheng; Sun, Yi; Jin, Yaguo; Li, Shuqing; Li, Zhaofu; Zou, Jianwen

    2017-06-01

    Soils are among the important sources of atmospheric nitric oxide (NO) and nitrous oxide (N 2 O), acting as a critical role in atmospheric chemistry. Updated data derived from 114 peer-reviewed publications with 520 field measurements were synthesized using meta-analysis procedure to examine the N fertilizer-induced soil NO and the combined NO+N 2 O emissions across global soils. Besides factors identified in earlier reviews, additional factors responsible for NO fluxes were fertilizer type, soil C/N ratio, crop residue incorporation, tillage, atmospheric carbon dioxide concentration, drought and biomass burning. When averaged across all measurements, soil NO-N fluxes were estimated to be 4.06 kg ha -1  yr -1 , with the greatest (9.75 kg ha -1  yr -1 ) in vegetable croplands and the lowest (0.11 kg ha -1  yr -1 ) in rice paddies. Soil NO emissions were more enhanced by synthetic N fertilizer (+38%), relative to organic (+20%) or mixed N (+18%) sources. Compared with synthetic N fertilizer alone, synthetic N fertilizer combined with nitrification inhibitors substantially reduced soil NO emissions by 81%. The global mean direct emission factors of N fertilizer for NO (EF NO ) and combined NO+N 2 O (EF c ) were estimated to be 1.16% and 2.58%, with 95% confidence intervals of 0.71-1.61% and 1.81-3.35%, respectively. Forests had the greatest EF NO (2.39%). Within the croplands, the EF NO (1.71%) and EF c (4.13%) were the greatest in vegetable cropping fields. Among different chemical N fertilizer varieties, ammonium nitrate had the greatest EF NO (2.93%) and EF c (5.97%). Some options such as organic instead of synthetic N fertilizer, decreasing N fertilizer input rate, nitrification inhibitor and low irrigation frequency could be adopted to mitigate soil NO emissions. More field measurements over multiyears are highly needed to minimize the estimate uncertainties and mitigate soil NO emissions, particularly in forests and vegetable croplands. © 2016 John Wiley

  2. Soil CO2 CH4 and N2O fluxes from an afforested lowland raised peatbog in Scotland: implications for drainage and restoration

    NASA Astrophysics Data System (ADS)

    Yamulki, S.; Anderson, R.; Peace, A.; Morison, J. I. L.

    2013-02-01

    The effect of tree (lodgepole pine) planting with and without intensive drainage on soil greenhouse gas (GHG) fluxes was assessed after 45 yr at a raised peatbog in West Flanders Moss, central Scotland. Fluxes of CO2 CH4 and N2O from the soil were monitored over a 2-yr period every 2 to 4 weeks using the static opaque chamber method in a randomised experimental block trial with the following treatments: drained and planted (DP), undrained and planted (uDP), undrained and unplanted (uDuP) and for reference also from an adjoining near-pristine area of bog at East Flanders Moss (n-pris). There was a strong seasonal pattern in both CO2 and CH4 effluxes which were significantly higher in late spring and summer months because of warmer temperatures. Effluxes of N2O were low and no significant differences were observed between the treatments. Annual CH4 emissions increased with the proximity of the water table to the soil surface across treatments in the order: DP < uDP < uDuP < n-pris with mean annual effluxes over the 2-yr monitoring period of 0.15, 0.64, 7.70 and 22.63 g CH4 m-2 yr-1, respectively. For CO2, effluxes increased in the order uDP < DP< n-pris < uDuP, with mean annual effluxes of 1.23, 1.66, 1.82 and 2.55 kg CO2 m-2 yr-1, respectively. CO2 effluxes dominated the total net GHG emission, calculated using the global warming potential (GWP) of the three GHGs for each treatment (76-98%), and only in the n-pris site was CH4 a substantial contribution (23%). Based on soil effluxes only, the near pristine (n-pris) peatbog had 43% higher total net GHG emission compared with the DP treatment because of high CH4 effluxes and the DP treatment had 33% higher total net emission compared with the uDP because drainage increased CO2 effluxes. Restoration is likely to increase CH4 emissions, but reduce CO2 effluxes. Our study suggests that if estimates of CO2 uptake by vegetation from similar peatbog sites were included, the total net GHG emission of restored peatbog would

  3. High CO2 emissions through porous media: Transport mechanisms and implications for flux measurement and fractionation

    USGS Publications Warehouse

    Evans, William C.; Sorey, M.L.; Kennedy, B.M.; Stonestrom, David A.; Rogie, J.D.; Shuster, D.L.

    2001-01-01

    Diffuse emissions of CO2 are known to be large around some volcanoes and hydrothermal areas. Accumulation-chamber measurements of CO2 flux are increasingly used to estimate the total magmatic or metamorphic CO2 released from such areas. To assess the performance of accumulation chamber systems at fluxes one to three orders of magnitude higher than normally encountered in soil respiration studies, a test system was constructed in the laboratory where known fluxes could be maintained through dry sand. Steady-state gas concentration profiles and fractionation effects observed in the 30-cm sand column nearly match those predicted by the Stefan-Maxwell equations, indicating that the test system was functioning successfully as a uniform porous medium. Eight groups of investigators tested their accumulation chamber equipment, all configured with continuous infrared gas analyzers (IRGA), in this system. Over a flux range of ~ 200-12,000 g m-2 day-1, 90% of their 203 flux measurements were 0-25% lower than the imposed flux with a mean difference of - 12.5%. Although this difference would seem to be within the range of acceptability for many geologic investigations, some potential sources for larger errors were discovered. A steady-state pressure gradient of -20 Pa/m was measured in the sand column at a flux of 11,200 g m-2 day-1. The derived permeability (50 darcies) was used in the dusty-gas model (DGM) of transport to quantify various diffusive and viscous flux components. These calculations were used to demonstrate that accumulation chambers, in addition to reducing the underlying diffusive gradient, severely disrupt the steady-state pressure gradient. The resultant diversion of the net gas flow is probably responsible for the systematically low flux measurements. It was also shown that the fractionating effects of a viscous CO2 efflux against a diffusive influx of air will have a major impact on some important geochemical indicators, such as N2/Ar, ??15N-N2, and 4He/22

  4. Microhabitat Effects on N2O Emissions from Floodplain Soils under Controlled Conditions

    NASA Astrophysics Data System (ADS)

    Ley, Martin; Lehmann, Moritz F.; Niklaus, Pascal A.; Kuhn, Thomas; Luster, Jörg

    2016-04-01

    tendency to emit more N2O than small-aggregate soils. Salix viminalis strongly suppressed the N2O emissions, fully compensating for any aggregate effects. Litter accumulation on the other hand enhanced N2O emission from well-aggregated soils, but showed only a small effect in combination with small aggregates. In moments of highest emission rates, the measured δ15Nbulk of headspace N2O was considerably lower relative to atmospheric N2O (δ15N between -20 ‰ and -25 ‰) in the amended treatments, suggesting N2O production by denitrification or by nitrifier-denitrification. Untreated mesocosms produced an even lower δ15Nbulk (-40‰). Similarly, aggregate formation/size seemed to affect the N2O δ15Nbulk values, suggesting different net N2O production dynamics under different microhabitat conditions, which will be elucidated further, using 15N site preference SP data. Combining stable isotope techniques with quantitative flux data from a mesoscale laboratory experiment, our data highlight the importance of microhabitat effects in modulating N2O emission from floodplain soils. It also underscores their influence on the N2O production pathways involved in the occurrence of N2O emission hot spots and moments.

  5. N2/O2/H2 Dual-Pump Cars: Validation Experiments

    NASA Technical Reports Server (NTRS)

    OByrne, S.; Danehy, P. M.; Cutler, A. D.

    2003-01-01

    The dual-pump coherent anti-Stokes Raman spectroscopy (CARS) method is used to measure temperature and the relative species densities of N2, O2 and H2 in two experiments. Average values and root-mean-square (RMS) deviations are determined. Mean temperature measurements in a furnace containing air between 300 and 1800 K agreed with thermocouple measurements within 26 K on average, while mean mole fractions agree to within 1.6 % of the expected value. The temperature measurement standard deviation averaged 64 K while the standard deviation of the species mole fractions averaged 7.8% for O2 and 3.8% for N2, based on 200 single-shot measurements. Preliminary measurements have also been performed in a flat-flame burner for fuel-lean and fuel-rich flames. Temperature standard deviations of 77 K were measured, and the ratios of H2 to N2 and O2 to N2 respectively had standard deviations from the mean value of 12.3% and 10% of the measured ratio.

  6. Understanding N2O sources and sinks with laser based isotopic analysis

    NASA Astrophysics Data System (ADS)

    Mohn, Joachim; Harris, Eliza; Tuzson, Béla; Emmenegger, Lukas

    2015-04-01

    Nitrous oxide (N2O) is a potent greenhouse gas and the strongest ozone-destroying substance. The main emissions of N2O are linked to different microbial processes, therefore the sources are disperse and highly variable, complicating the development of effective mitigation strategies. Isotopic measurements have great potential to unravel spatial and temporal variations in sources, sinks and chemistry of N2O. Recent developments in quantum cascade laser spectroscopy (QCLAS) [1] allow both the intermolecular distribution of 15N substitutions ('site preference'; 15N14N16O versus 14N15N16O) and the oxygen isotopic composition (d18O) of N2O to be measured in real-time and at high precision of <0.2 ‰ [2]. Additionally, N2O isotopic analysis by QCLAS has demonstrated excellent compatibility to the standard technique isotope-ratio mass-spectrometry [3]. In a number of laboratory and pilot plant studies we investigated the isotopic signature of distinct microbial and abiotic N2O production and consumption pathways in soil and aqueous solution [e.g. 4]. Specific pathways were favoured by selection of the nitrogen substrates and process conditions and their isotopic signatures identified by real-time laser spectroscopic analysis. Results from our laboratory studies are in accordance with pure culture experiments and can therefore be applied to other ecosystems. Recently, high precision isotopic analysis at ambient N2O is also feasible by combining laser spectroscopy with automated preconcentration [5]. The field deployment was demonstrated by real-time monitoring isotopic composition of N2O emissions from an intensively managed grassland in central Switzerland for three months. The responses of the N2O isotopic signatures were analysed with respect to management events and weather influences [2]. In a follow-up project we intend to combine real-time N2O isotopic analysis at a tall tower in central Switzerland with atmospheric transport simulations and a biogeochemical model

  7. Nitrogen availability and soil N2O emissions following conversion of forests to coffee in southern Sumatra

    NASA Astrophysics Data System (ADS)

    Verchot, Louis V.; Hutabarat, Lusida; Hairiah, Kurniatun; van Noordwijk, Meine

    2006-12-01

    Changes in land use impact on the N cycle with both local and global consequences. We examined how conversion of forest to agriculture in one catchment in southern Sumatra altered N availability and soil N2O emission. Measurements were made along a chronosequence of forest land converted to coffee gardens. A number of different management practices were also examined. Inorganic N stocks and N cycling rates were highest in the forest and lower in the coffee gardens. The forest and young conversion sites appeared to be N limited, whereas the older agricultural sites and the more intensively managed sites were not as strongly N limited. N2O emissions were low in the forest (<2 kgN ha-1yr-1) and increased sharply following deforestation. Emissions on recently cleared land were 4.6 kgN ha-1yr-1 and 8.4 kgN ha-1yr-1 in a 1-year-old coffee garden. Emissions in the older coffee gardens were lower with the lowest flux observed in a 10 year old site (1.8 kgN ha-1yr-1). We explored the effects of different types of management approaches that farmers are using in this landscape. Emissions in an 18-year-old multistrata coffee garden with a significant overstory of N fixing trees were 5 times greater (15.5 kg ha-1yr-1) than emissions from forests. We also found that intensive organic matter management produced high emissions. To understand the spatial and temporal variability of the N2O emissions we used the hole-in-the-pipe conceptual model. N2O fluxes were lowest on N limited sites. Soil water content also played an important role and emissions were highest when water filled pore space (WFPS) was between 85 and 95%. A number of formulations of this model have been applied in different ways over the years to explain spatial and temporal variation in the soil N-oxide flux, and in this study we found the mechanistic explanation useful. Our study suggests that land use change and intensification of agriculture in N limited highland landscapes may significantly increase the

  8. Spatial variability in groundwater N2 and N2O in the San Joaquin River

    NASA Astrophysics Data System (ADS)

    Hinshaw, S.; Dahlgren, R. A.

    2010-12-01

    The San Joaquin River is surrounded by nearly 2 million acres of irrigated agricultural land. Groundwater inputs from agricultural areas can have severe negative effects on water quality with high nitrate concentrations being a major concern. Riparian zones are important ecological habitats that mitigate nitrogen loading from groundwater discharging into rivers primarily by denitrification. Denitrification is a permanent removal of nitrate by anaerobic microbial communities via the reduction to NO, N2O and N2. However, previous studies have shown that these areas can be source of N2O emissions. Although removal of nitrate through denitrification is advantageous from a water quality perspective, N2O is a harmful greenhouse gas. This study aimed to investigate nitrogen dynamics and dissolved N gases in surface and groundwater of the riparian zones of the San Joaquin River. Excess N2 and N2O concentrations were measured in surface and groundwater at 4 locations along a 33 km reach of the river. Samples were collected within bank sediments and 5 transect points across the river at depth intervals between 2-3 cm and 150 cm. Dissolved N2 and Ar were measured by membrane inlet mass spectrometry and used to estimate excess dissolved N2 concentrations. Dissolved N2O concentrations were measured using the headspace equilibrium technique and analyzed with a gas chromatograph. Both N2 uptake and excess N2 were present, ranging from -3.40 to 8.65 N2 mg/L with a median concentration of 1.20 N2 mg/L. Significantly lower concentrations of N2O were present ranging from 0.0 to 0.12 N2O mg/L. Deeper groundwater sites had significantly higher N2 and N2O concentrations coinciding with decreased O2. The presence of excess N2 and low N2O concentrations documents the importance of denitrification in removing nitrate from groundwater. Further investigation will examine N2O emissions from riparian soils and benthic sediments using static chambers and focus on nitrogen pathways that

  9. Stratospheric CFCl3, CF2Cl2, and N2O height profile measurements at several latitudes

    NASA Astrophysics Data System (ADS)

    Goldan, P. D.; Kuster, W. C.; Albritton, D. L.; Schmeltekopf, A. L.

    1980-01-01

    The mixing ratios of CFCl3, CF2Cl2, and N2O have been measured as a function of altitude from 6 to 37 km above sea level by using a balloon-borne grab-sampling system. The 24 flights were made during the period July 1976 to March 1979 from Wyoming, Panama, Brazil, and Antarctica. These data are reported here both numerically and graphically, the latter being examined for latitudinal and temporal trends. A mean tropopause height for each location and date was used as the reference for the height profiles. The resulting set of CF2Cl2 and N2O profiles show a discernible dependence on latitude; the lapse rate of these mixing ratios is greater for the mid-latitudes when compared to the equatorial latitudes. The upper tropospheric portion of the CFCl3 and CF2Cl2 data show annual increases of 10.4±3.9 and 10.7±1.9%/yr, respectively, in the northern hemisphere for the middle of the measurement period (end of 1977). Furthermore, the limited number of southern hemispheric data for these constituents are about 8% lower than the northern hemispheric values but have a comparable annual increase. The corresponding N2O data show no interhemispheric differences and the possibility of only a slight increase (less than 2%/yr).

  10. Airborne Solar Radiant Flux Measurements During ACE-2

    NASA Technical Reports Server (NTRS)

    Bergstrom, Robert W.; Russell, Philip B.; Jonsson, Haflidi

    2000-01-01

    Aerosol effects on atmospheric radiative fluxes provide a forcing function that can change the climate in potentially significant ways. This aerosol radiative forcing is a major source of uncertainty in understanding the climate change of the past century and predicting future climate. To help reduce this uncertainty, the 1996 Tropospheric Aerosol Radiative Forcing Observational Experiment (TARFOX) and the 1997 Aerosol Characterization Experiment (ACE-2) measured the properties and radiative effects of aerosols over the Atlantic Ocean. In the ACE 2 program the solar radiant fluxes were measured on the Pelican aircraft and the UK Met Office C130. This poster will show results from the measurements for the aerosol effects during the clear column days. We will compare the results with calculations of the radiant fluxes.

  11. Carbon availability and the distribution of denitrifying organisms influence N2O production in the hyporheic zone

    NASA Astrophysics Data System (ADS)

    Farrell, T. B.; Quick, A. M.; Reeder, W. J.; Tonina, D.; Benner, S. G.; Feris, K. P.

    2013-12-01

    It has been estimated that 10% of greenhouse gas N2O emissions take place within river networks, with the majority of these processes occurring in the hyporheic zone (HZ). These emissions are the result of microbially-mediated nitrogen transformations (i.e. nitrification and denitrification) and yet the role of microbial distribution and function in this complex system is not well understood. We hypothesized that the concentration and availability of organic carbon influences the production of redox gradients, DIN (via mineralization, nitrification, and loss of DIN via denitrification), and ultimately N2O production in the HZ by controlling the distribution and activity of denitrifying microbial communities. Further, we hypothesized that by linking the distribution of denitrifying microbial communities and their associated functional genes (i.e. the relative abundance of N2O vs. N2 producing genetic elements) to flow dynamics and biogeochemical processes, we can begin to better understand what controls N2O production in hyporheic networks. To address these hypotheses we performed a series of column experiments designed to determine the influence of carbon concentration on redox gradient development and N2O flux along a one-dimensional flow path. Intact sediment cores were amended with 0.01%, 0.05%, 0.15%, and 0.5% dry mass riparian vegetation (>90% Populus sp.) to serve as an endogenous particulate organic matter (POM) source. During quasi-steady state conditions dissolved oxygen (DO), NH4+, NO3-, and N2O levels were measured. As predicted, a positive relationship between the level of POM amendment and development of a gradient of oxic and anoxic conditions was observed. There was negligible N2O production within columns inoculated with 0.01% and 0.05% DOC likely because these POC treatments were too low to create anoxic conditions necessary to stimulate denitrification. Maximum N2O flux was observed with the 0.15% POC treatment. Both oxic and anoxic conditions

  12. Production of N2O/+/ by reaction of metastable O2/+/ ions with N2

    NASA Technical Reports Server (NTRS)

    Ajello, J. M.; Rayermann, P.

    1975-01-01

    Photoionization mass spectrometry examination of the production of N2O(+) was undertaken to determine whether N2(+) or O2(+) ions are responsible for onset of N2O(+). It appears that the N2(+) ion does not contribute significantly to the production of N2O(+) in this experiment. Therefore, it is clear that excited O2(+) is responsible for the formation of N2O(+) near the appearance potential of these ions.

  13. Are dual isotope and isotopomer ratios of N2O useful indicators for N2O turnover during denitrification in nitrate-contaminated aquifers?

    NASA Astrophysics Data System (ADS)

    Well, Reinhard; Eschenbach, Wolfram; Flessa, Heinz; von der Heide, Carolin; Weymann, Daniel

    2012-08-01

    contribution of different processes to the total N2O flux, apparently because these values were not only governed by individual pathways but eventually also by the spatial distribution of substrates and activity within the aquifers. These observations could be explained by the dynamics of N2O production, reduction and transport in water-saturated systems with heterogenic distribution of microbial activity and by a combination of diffusive and enzymatic isotope effects.

  14. N2O emissions from a nitrogen-enriched river

    USGS Publications Warehouse

    McMahon, P.B.; Dennehy, K.F.

    1999-01-01

    Nitrous oxide (N2O) emissions from the South Platte River in Colorado were measured using closed chambers in the fall, winter, and summer of 1994- 1995. The South Platte River was enriched in inorganic N (9-800 ??M) derived from municipal wastewater effluent and groundwater return flows from irrigated agricultural fields. River water was as much as 2500% supersaturated with N2O, and median N2O emission rates from the river surface ranged from less than 90 to 32 600 ??g-N m-2 d-1. Seventy-nine percent of the variance in N2O emission rates was explained by concentrations of total inorganic N in river water and by water temperature. The estimated total annual N2O emissions from the South Platte River were 2 x 1013-6 x 1013 ??g-N yr-1. This amount of annual N2O emissions was similar to the estimated annual N2O emissions from all primary municipal wastewater treatment processes in the United States (1). Results from this study indicate that N-enriched rivers could be important anthropogenic sources of N2O to the atmosphere. However, N2O emission measurements from other N-enriched rivers are needed to better quantify this source.Nitrous oxide (N2O) emissions from the South Platte River in Colorado were measured using closed chambers in the fall, winter, and summer of 1994-1995. The South Platte River was enriched in inorganic N (9-800 ??M) derived from municipal wastewater effluent and groundwater return flows from irrigated agricultural fields. River water was as much as 2500% supersaturated with N2O, and median N2O emission rates from the river surface ranged from less than 90 to 32 600 ??g-N m-2 d-1. Seventy-nine percent of the variance in N2O emission rates was explained by concentrations of total inorganic N in river water and by water temperature. The estimated total annual N2O emissions from the South Platte River were 2??1013-6??1013 ??g-N yr-1. This amount of annual N2O emissions was similar to the estimated annual N2O emissions from all primary municipal

  15. Influence of aerosol chemical composition on N2O5 uptake: airborne regional measurements in northwestern Europe

    NASA Astrophysics Data System (ADS)

    Morgan, W. T.; Ouyang, B.; Allan, J. D.; Aruffo, E.; Di Carlo, P.; Kennedy, O. J.; Lowe, D.; Flynn, M. J.; Rosenberg, P. D.; Williams, P. I.; Jones, R.; McFiggans, G. B.; Coe, H.

    2015-01-01

    Aerosol chemical composition was found to influence nighttime atmospheric chemistry during a series of airborne measurements in northwestern Europe in summer conditions, which has implications for regional air quality and climate. The uptake of dinitrogen pentoxide, γ (N2O5), to particle surfaces was found to be modulated by the amount of water content and ammonium nitrate present in the aerosol. The conditions prevalent in this study suggest that the net uptake rate of N2O5 to atmospheric aerosols was relatively efficient compared to previous studies, with γ (N2O5) values in the range 0.01-0.03. This is likely a consequence of the elevated relative humidity in the region, which promotes greater aerosol water content. Increased nitrate concentrations relative to particulate water were found to suppress N2O5 uptake. The results presented here contrast with previous ambient studies of N2O5 uptake, which have generally taken place in low-nitrate environments in the USA. Comparison of the N2O5 uptake derived from the measurements with a parameterised scheme that is based on the ratio of particulate water to nitrate yielded reasonably good agreement in terms of the magnitude and variation in uptake, provided the effect of chloride was neglected. An additional suppression of the parameterised uptake is likely required to fully capture the variation in N2O5 uptake, which could be achieved via the known suppression by organic aerosol. However, existing parameterisations representing the suppression by organic aerosol were unable to fully represent the variation in N2O5 uptake. These results provide important ambient measurement constraint on our ability to predict N2O5 uptake in regional and global aerosol models. N2O5 uptake is a potentially important source of nitrate aerosol and a sink of the nitrate radical, which is the main nocturnal oxidant in the atmosphere. The results further highlight the importance of ammonium nitrate in northwestern Europe as a key component

  16. Soil invertebrate fauna affect N2 O emissions from soil.

    PubMed

    Kuiper, Imke; de Deyn, Gerlinde B; Thakur, Madhav P; van Groenigen, Jan Willem

    2013-09-01

    Nitrous oxide (N2 O) emissions from soils contribute significantly to global warming. Mitigation of N2 O emissions is severely hampered by a lack of understanding of its main controls. Fluxes can only partly be predicted from soil abiotic factors and microbial analyses - a possible role for soil fauna has until now largely been overlooked. We studied the effect of six groups of soil invertebrate fauna and tested the hypothesis that all of them increase N2 O emissions, although to different extents. We conducted three microcosm experiments with sandy soil and hay residue. Faunal groups included in our experiments were as follows: fungal-feeding nematodes, mites, springtails, potworms, earthworms and isopods. In experiment I, involving all six faunal groups, N2 O emissions declined with earthworms and potworms from 78.4 (control) to 37.0 (earthworms) or 53.5 (potworms) mg N2 O-N m(-2) . In experiment II, with a higher soil-to-hay ratio and mites, springtails and potworms as faunal treatments, N2 O emissions increased with potworms from 51.9 (control) to 123.5 mg N2 O-N m(-2) . Experiment III studied the effect of potworm density; we found that higher densities of potworms accelerated the peak of the N2 O emissions by 5 days (P < 0.001), but the cumulative N2 O emissions remained unaffected. We propose that increased soil aeration by the soil fauna reduced N2 O emissions in experiment I, whereas in experiment II N2 O emissions were driven by increased nitrogen and carbon availability. In experiment III, higher densities of potworms accelerated nitrogen and carbon availability and N2 O emissions, but did not increase them. Overall, our data show that soil fauna can suppress, increase, delay or accelerate N2 O emissions from soil and should therefore be an integral part of future N2 O studies. © 2013 John Wiley & Sons Ltd.

  17. Characterization and production and consumption processes of N2O emitted from temperate agricultural soils determined via isotopomer ratio analysis

    NASA Astrophysics Data System (ADS)

    Toyoda, Sakae; Yano, Midori; Nishimura, Sei-Ichi; Akiyama, Hiroko; Hayakawa, Atsushi; Koba, Keisuke; Sudo, Shigeto; Yagi, Kazuyuki; Makabe, Akiko; Tobari, Yoshifumi; Ogawa, Nanako O.; Ohkouchi, Naohiko; Yamada, Keita; Yoshida, Naohiro

    2011-06-01

    Isotopomer ratios of N2O (bulk nitrogen and oxygen isotope ratios, δ15Nbulk and δ18O, and intramolecular 15N site preference, SP) are useful parameters that characterize sources of this greenhouse gas and also provide insight into production and consumption mechanisms. We measured isotopomer ratios of N2O emitted from typical Japanese agricultural soils (Fluvisols and Andisols) planted with rice, wheat, soybean, and vegetables, and treated with synthetic (urea or ammonium) and organic (poultry manure) fertilizers. The results were analyzed using a previously reported isotopomeric N2O signature produced by nitrifying/denitrifying bacteria and a characteristic relationship between δ15Nbulk and SP during N2O reduction by denitrifying bacteria. Relative contributions from nitrification (hydroxylamine oxidation) and denitrification (nitrite reduction) to gross N2O production deduced from the analysis depended on soil type and fertilizer. The contribution from nitrification was relatively high (40%-70%) in Andisols amended with synthetic ammonium fertilizer, while denitrification was dominant (50%-90%) in the same soils amended with poultry manure during the period when N2O production occurred in the surface layer. This information on production processes is in accordance with that obtained from flux/concentration analysis of N2O and soil inorganic nitrogen. However, isotopomer analysis further revealed that partial reduction of N2O was pronounced in high-bulk density, alluvial soil (Fluvisol) compared to low-bulk density, volcanic ash soil (Andisol), and that the observed difference in N2O flux between normal and pelleted manure could have resulted from a similar mechanism with different rates of gross production and gross consumption. The isotopomeric analysis is based on data from pure culture bacteria and would be improved by further studies on in situ biological processes in soils including those by fungi. When flux/concentration-weighted average isotopomer

  18. Complete Measurement of Stable Isotopes in N2O (δ15N, δ15Nα, δ15Nβ, δ18O, δ17O) Using Off-Axis Integrated Cavity Output Spectroscopy (OA-ICOS)

    NASA Astrophysics Data System (ADS)

    Leen, J. B.; Gupta, M.

    2014-12-01

    Nitrate contamination in water is a worldwide environmental problem and source apportionment is critical to managing nitrate pollution. Fractionation caused by physical, chemical and biological processes alters the isotope ratios of nitrates (15N/14N, 18O/16O and 17O/16O) and biochemical nitrification and denitrification impart different intramolecular site preference (15N14NO vs. 14N15NO). Additionally, atmospheric nitrate is anomalously enriched in 17O compared to other nitrate sources. The anomaly (Δ17O) is conserved during fractionation processes, providing a tracer of atmospheric nitrate. All of these effects can be used to apportion nitrate in soil. Current technology for measuring nitrate isotopes is complicated and costly - it involves conversion of nitrate to nitrous oxide (N2O), purification, preconcentration and measurement by isotope ratio mass spectrometer (IRMS). Site specific measurements require a custom IRMS. There is a pressing need to make this measurement simpler and more accessible. Los Gatos Research has developed a next generation mid-infrared Off-Axis Integrated Cavity Output Spectroscopy (OA-ICOS) analyzer to quantify all stable isotope ratios of N2O (δ15N, δ15Nα, δ15Nβ, δ18O, δ17O). We present the latest performance data demonstrating the precision and accuracy of the OA-ICOS based measurement. At an N2O concentration of 322 ppb, the analyzer quantifies [N2O], δ15N, δ15Na, δ15Nb, and δ18O with a precision of ±0.05 ppb, ±0.4 ‰, ±0.45 ‰, and ±0.6 ‰, and ±0.8 ‰ respectively (1σ, 100s; 1σ, 1000s for δ18O). Measurements of gas standards demonstrate accuracy better than ±1 ‰ for isotope ratios over a wide dynamic range (200 - 100,000 ppb). The measurement of δ17O requires a higher concentration (1 - 50 ppm), easily obtainable through conversion of nitrates in water. For 10 ppm of N2O, the instrument achieves a δ17O precision of ±0.05 ‰ (1σ, 1000s). This performance is sufficient to quantify atmospheric

  19. Response of nitric and nitrous oxide fluxes to N fertilizer application in greenhouse vegetable cropping systems in southeast China

    PubMed Central

    Zhang, Yaojun; Lin, Feng; Jin, Yaguo; Wang, Xiaofei; Liu, Shuwei; Zou, Jianwen

    2016-01-01

    It is of great concern worldwide that active nitrogenous gases in the global nitrogen cycle contribute to regional and global-scale environmental issues. Nitrous oxide (N2O) and nitric oxide (NO) are generally interrelated in soil nitrogen biogeochemical cycles, while few studies have simultaneously examined these two gases emission from typical croplands. Field experiments were conducted to measure N2O and NO fluxes in response to chemical N fertilizer application in annual greenhouse vegetable cropping systems in southeast China. Annual N2O and NO fluxes averaged 52.05 and 14.87 μg N m−2 h−1 for the controls without N fertilizer inputs, respectively. Both N2O and NO emissions linearly increased with N fertilizer application. The emission factors of N fertilizer for N2O and NO were estimated to be 1.43% and 1.15%, with an annual background emission of 5.07 kg N2O-N ha−1 and 1.58 kg NO-N ha−1, respectively. The NO-N/N2O-N ratio was significantly affected by cropping type and fertilizer application, and NO would exceed N2O emissions when soil moisture is below 54% WFPS. Overall, local conventional input rate of chemical N fertilizer could be partially reduced to attain high yield of vegetable and low N2O and NO emissions in greenhouse vegetable cropping systems in China. PMID:26848094

  20. Response of nitric and nitrous oxide fluxes to N fertilizer application in greenhouse vegetable cropping systems in southeast China.

    PubMed

    Zhang, Yaojun; Lin, Feng; Jin, Yaguo; Wang, Xiaofei; Liu, Shuwei; Zou, Jianwen

    2016-02-05

    It is of great concern worldwide that active nitrogenous gases in the global nitrogen cycle contribute to regional and global-scale environmental issues. Nitrous oxide (N2O) and nitric oxide (NO) are generally interrelated in soil nitrogen biogeochemical cycles, while few studies have simultaneously examined these two gases emission from typical croplands. Field experiments were conducted to measure N2O and NO fluxes in response to chemical N fertilizer application in annual greenhouse vegetable cropping systems in southeast China. Annual N2O and NO fluxes averaged 52.05 and 14.87 μg N m(-2) h(-1) for the controls without N fertilizer inputs, respectively. Both N2O and NO emissions linearly increased with N fertilizer application. The emission factors of N fertilizer for N2O and NO were estimated to be 1.43% and 1.15%, with an annual background emission of 5.07 kg N2O-N ha(-1) and 1.58 kg NO-N ha(-1), respectively. The NO-N/N2O-N ratio was significantly affected by cropping type and fertilizer application, and NO would exceed N2O emissions when soil moisture is below 54% WFPS. Overall, local conventional input rate of chemical N fertilizer could be partially reduced to attain high yield of vegetable and low N2O and NO emissions in greenhouse vegetable cropping systems in China.

  1. Low-Temperature Desorption of N2O from NO on Rutile TiO2(110)-1x1

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    Kim, Boseong; Li, Zhenjun; Kay, Bruce D.

    2014-05-08

    We find that NO dosed on rutile TiO2(110)-1×1 at substrate temperatures as low as 50 K readily reacts to produce N2O which desorbs promptly from the surface leaving an oxygen adatom behind. The desorption rate of N2O reaches a maximum value after 1 – 2 sec at an NO flux of 1.2 ×1014 NO/cm2∙sec and then decreases rapidly as the initially clean, reduced TiO2(110) surface with ~5% oxygen vacancies (VO’s) becomes covered with oxygen adatoms and unreacted NO. The maximum desorption rate is also found to increase as the substrate temperature is raised up to about 100 K. Interestingly, themore » N2O desorption during the low-temperature (LT) NO dose is strongly suppressed when molecular oxygen is predosed, whereas it persists on the surface with VO’s passivated by surface hydroxyls. Our results show that the surface charge, not the VO sites, plays a dominant role in the LT N2O desorption induced by a facile NO reduction at such low temperatures.« less

  2. Diode laser measurements of linestrength and temperature-dependent lineshape parameters of H2O-, CO2-, and N2-perturbed H2O transitions near 2474 and 2482 nm

    NASA Astrophysics Data System (ADS)

    Goldenstein, Christopher S.; Jeffries, Jay B.; Hanson, Ronald K.

    2013-11-01

    Absorption lineshapes for two unresolved H2O doublets near 4029.52 and 4041.92 cm-1 were measured at high-resolution in a heated static cell using two distributed-feedback diode lasers. Measurements were acquired for H2O, CO2, and N2 perturbers over a temperature and pressure range of 650-1325 K and 2-760 Torr, respectively. Strong collisional narrowing effects were observed in CO2 and N2, but not in pure H2O. The Galatry profile was used to infer collisional-broadening and -narrowing coefficients and their respective temperature dependence for CO2 and N2 perturbers. The collisional-broadening and -narrowing coefficients for CO2 perturbers were found to decrease with increasing temperature in a similar manner. For N2 perturbers, the collisional-broadening coefficients increased with temperature while the collisional-narrowing coefficients decreased with increasing temperature. Self-broadening coefficients were inferred from Voigt profile fits and are compared with HITEMP 2010. The linestrengths of 17 H2O transitions are also reported.

  3. Iron cation catalyzed reduction of N2O by CO: gas-phase temperature dependent kinetics.

    PubMed

    Melko, Joshua J; Ard, Shaun G; Fournier, Joseph A; Li, Jun; Shuman, Nicholas S; Guo, Hua; Troe, Jürgen; Viggiano, Albert A

    2013-07-21

    The ion-molecule reactions Fe(+) + N2O → FeO(+) + N2 and FeO(+) + CO → Fe(+) + CO2, which catalyze the reaction CO + N2O → CO2 + N2, have been studied over the temperature range 120-700 K using a variable temperature selected ion flow tube apparatus. Values of the rate constants for the former two reactions were experimentally derived as k2 (10(-11) cm(3) s(-1)) = 2.0(±0.3) (T/300)(-1.5(±0.2)) + 6.3(±0.9) exp(-515(±77)/T) and k3 (10(-10) cm(3) s(-1)) = 3.1(±0.1) (T/300)(-0.9(±0.1)). Characterizing the energy parameters of the reactions by density functional theory at the B3LYP/TZVP level, the rate constants are modeled, accounting for the intermediate formation of complexes. The reactions are characterized by nonstatistical intrinsic dynamics and rotation-dependent competition between forward and backward fluxes. For Fe(+) + N2O, sextet-quartet switching of the potential energy surfaces is quantified. The rate constant for the clustering reaction FeO(+) + N2O + He → FeO(N2O)(+) + He was also measured, being k4 (10(-27) cm(6) s(-1)) = 1.1(±0.1) (T/300)(-2.5(±0.1)) in the low pressure limit, and analyzed in terms of unimolecular rate theory.

  4. Valence band offset of β-Ga2O3/wurtzite GaN heterostructure measured by X-ray photoelectron spectroscopy.

    PubMed

    Wei, Wei; Qin, Zhixin; Fan, Shunfei; Li, Zhiwei; Shi, Kai; Zhu, Qinsheng; Zhang, Guoyi

    2012-10-10

    A sample of the β-Ga2O3/wurtzite GaN heterostructure has been grown by dry thermal oxidation of GaN on a sapphire substrate. X-ray diffraction measurements show that the β-Ga2O3 layer was formed epitaxially on GaN. The valence band offset of the β-Ga2O3/wurtzite GaN heterostructure is measured by X-ray photoelectron spectroscopy. It is demonstrated that the valence band of the β-Ga2O3/GaN structure is 1.40 ± 0.08 eV.

  5. Measuring and modeling of soil N2O emissions - How well are we doing?

    NASA Astrophysics Data System (ADS)

    Butterbach-Bahl, K.; Ralf, K.; Werner, C.; Wolf, B.

    2017-12-01

    Microbial processes in soils are the primarily source of atmospheric N2O. Fertilizer use to boost food and feed production of agricultural systems as well as nitrogen deposition to natural and semi-natural ecosystems due to emissions of NOx and NH3 from agriculture and energy production and re-deposition to terrestrial ecosystems has likely nearly doubled the pre-industrial source strength of soils for atmospheric N2O. Quantifying soil emissions and identifying mitigation options is becoming a major focus in the climate debate as N2O emissions from agricultural soils are a major contributor to the greenhouse gas footprint of agricultural systems, with agriculture incl. land use change contributing up to 30% to total anthropogenic GHG emissions. The increasing number of annual datasets show that soil emissions a) are largely depended on soil N availability and thus e.g. fertilizer application, b) vary with management (e.g. timing of fertilization, residue management, tillage), c) depend on soil properties such as organic matter content and pH, e) are affected by plant N uptake, and e) are controlled by environmental factors such as moisture and temperature regimes. It is remarkable that the magnitude of annual emissions is largely controlled by short-term N2O pulses occurring due to fertilization, wetting and drying or freezing and thawing of soils. All of this contributes to a notorious variability of soil N2O emissions in space and time. Overcoming this variability for quantification of source strengths and identifying tangible mitigation options requires targeted measuring approaches as well as the translation of our knowledge on mechanisms underlying emissions into process oriented models, which finally might be used for upscaling and scenario studies. This paper aims at reviewing current knowledge on measurements, modelling and upscaling of soil N2O emissions, thereby identifying short comes and uncertainties of the various approaches and fields for future

  6. CO2 CH4 and N20 fluxes during land conversion in early bioenergy systems

    NASA Astrophysics Data System (ADS)

    Zenone, T.

    2012-04-01

    CO2 CH4 and N20 fluxes during land conversion in early bioenergy systems Terenzio Zenone1-2, Jiquan Chen1-2, Ilya Gelfand3-4, G. Philip Robertson3-4 1 Department of Environmental Sciences, University of Toledo, Toledo, OH USA 2 Great Lakes Bioenergy Research Center, Michigan State University, East Lansing, MI USA 3 W.K. Kellogg Biological Station, Michigan State University, Hickory Corners, MI USA 4Department of Crop and Soil Sciences, Michigan State University, East Lansing, MI USA Environmental sustainability of bioenergy crop cultivation represents an important challenge and is a topic of intensive scientific and political debate worldwide due to increasing societal needs for renewable energy. Despite the increasing knowledge related to potential bioenergy systems, the effect of land use change (LUC) on GHG fluxes during the conversion remains poorly understood but is likely to be substantial. In order to tackle this issue the Great lake Bioenergy Research Center (GLBRC) of the US Department of Energy (DOE) has established a field experiment and deployed a cluster of eddy-covariance towers to quantify the magnitude and changes of ecosystem carbon assimilation, loss, and balance during the conversion and establishment years in a permanent prairie and four types of candidate biofuel systems [Conservation Reserve Program (CRP) grassland, switchgrass, mixed-species restored prairie and corn]. Six sites were converted to soybean in 2009 before establishing the bioenergy systems in 2010 while one site was kept grassland as reference. Soil N2O and CH4 fluxes were measured biweekly with static chambers in four replicate locations in each fields, within the footprint of the eddy covariance tower using static chamber GHG flux protocols of the KBS LTER site. Our field observations, made between January 2009 through December 2010, showed that conversion of CRP to soybean induced net C emissions during the conversion year that ranging from 288 g C m-2, to 173 g C m-2 . while

  7. A high-resolution measurement technique for vertical CO2 and H2O profiles within and above crop canopies and its use for flux partitioning

    NASA Astrophysics Data System (ADS)

    Ney, Patrizia; Schmidt, Marius; Klosterhalfen, Anne; Graf, Alexander

    2017-04-01

    We present a portable elevator-based setup for measuring CO2, water vapor, temperature and wind profiles from the soil surface to the surface layer above crop canopies. The end of a tube connected to a closed-path gas analyzer is continuously moved up and down over the profile height (currently 2 m), while concentrations are logged at a frequency of 20 Hz. Temperature and wind speed are measured at the same frequency by a ventilated finewire thermocouple and a hotwire, respectively, and all measurements are duplicated as a continuous fixed-height measurement at the top of the profile. Test measurements were carried out at the TERENO research site of Selhausen (50°52'09"N, 06°27'01"E, 104.5 m MSL, Germany, ICOS site DE-RuS) in winter wheat, winter barley and a catch crop mixture during different stages of crop development and different times of the day (spring 2015 to autumn 2016). We demonstrate a simple approach to correct for time lags, and the resulting half-hourly mean profiles of CO2 and H2O over height increments of 2.5 cm. These results clearly show the effects of soil respiration and photosynthetic carbon assimilation, varying both during the daily cycle and during the growing season. Post-harvest measurements over bare soil and short intercrop canopy (<20 cm) were analyzed in the framework of Monin-Obukhov similarity theory to check the validity of the measurement and raw data processing approach. Derived CO2 and latent heat fluxes show a good agreement to eddy-covariance measurements. In a next step, we applied a dispersion matrix inversion (modified after Warland and Thurtell 2000, Santos et al. 2011) to the concentration profiles to estimate the vertical source and sink distribution of CO2 and H2O. First results showed reasonable values for evaporation, transpiration and aboveground net primary production, but a likely overestimation of soil respiration. We discuss possible causes associated with exchange processes near the soil surface below a dense

  8. Microwave dielectric properties of BaO-2CeO{sub 2}-nTiO{sub 2} ceramics

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    Sreemoolanadhan, H.; Sebastian, M.T.; Ratheesh, R.

    2004-11-01

    The BaO-2CeO{sub 2}-nTiO{sub 2} ceramics with n=3, 4 and 5 have been prepared with CeO{sub 2} as starting material. The ceramics have been characterized using scanning electron microscopy, X-ray diffraction, Raman and X-ray photoelectron spectroscopy techniques. The microwave dielectric properties have been measured using standard dielectric resonator techniques. BaO-2CeO{sub 2}-3TiO{sub 2} (123), BaO-2CeO{sub 2}-4TiO{sub 2} (124) and BaO-2CeO{sub 2}-5TiO{sub 2} (125) ceramics showed dielectric constants of 38, 27 and 32, respectively. All the ceramics showed fairly good unloaded Q-factors. 124 and 125 compounds exhibited low {tau}f values, while 123 showed a high {tau}f value.

  9. True eddy accumulation and eddy covariance methods and instruments intercomparison for fluxes of CO2, CH4 and H2O above the Hainich Forest

    NASA Astrophysics Data System (ADS)

    Siebicke, Lukas

    2017-04-01

    The eddy covariance (EC) method is state-of-the-art in directly measuring vegetation-atmosphere exchange of CO2 and H2O at ecosystem scale. However, the EC method is currently limited to a small number of atmospheric tracers by the lack of suitable fast-response analyzers or poor signal-to-noise ratios. High resource and power demands may further restrict the number of spatial sampling points. True eddy accumulation (TEA) is an alternative method for direct and continuous flux observations. Key advantages are the applicability to a wider range of air constituents such as greenhouse gases, isotopes, volatile organic compounds and aerosols using slow-response analyzers. In contrast to relaxed eddy accumulation (REA), true eddy accumulation (Desjardins, 1977) has the advantage of being a direct method which does not require proxies. True Eddy Accumulation has the potential to overcome above mentioned limitations of eddy covariance but has hardly ever been successfully demonstrated in practice in the past. This study presents flux measurements using an innovative approach to true eddy accumulation by directly, continuously and automatically measuring trace gas fluxes using a flow-through system. We merge high-frequency flux contributions from TEA with low-frequency covariances from the same sensors. We show flux measurements of CO2, CH4 and H2O by TEA and EC above an old-growth forest at the ICOS flux tower site "Hainich" (DE-Hai). We compare and evaluate the performance of the two direct turbulent flux measurement methods eddy covariance and true eddy accumulation using side-by-side trace gas flux observations. We further compare performance of seven instrument complexes, i.e. combinations of sonic anemometers and trace gas analyzers. We compare gas analyzers types of open-path, enclosed-path and closed-path design. We further differentiate data from two gas analysis technologies: infrared gas analysis (IRGA) and laser spectrometry (open path and CRDS closed

  10. Investigation the influences of B2O3 and R2O on the structure and crystallization behaviors of CaO-Al2O3 based F-free mold flux

    NASA Astrophysics Data System (ADS)

    Li, Jiangling; Kong, Bowen; Gao, Xiangyu; Liu, Qingcai; Shu, Qifeng; Chou, Kuochih

    2018-04-01

    The influences of B2O3 and R2O on the structure and crystallization of CaO-Al2O3 based F-free mold flux were investigated by Raman Spectroscopy and Differential Scanning Calorimetry Technique, respectively, for developing a new type of F-free mold flux. The results of structural investigations showed that B3+ is mainly in the form of [BO3]. And [BO3] appears to form BIII-O-Al linkage which will produce a positive effect on forming [AlO4] network. The number of bridging oxygen and the degree of polymerization of [AlO4] network structure for CaO-Al2O3 system were also increased with the increasing of B2O3. On the contrary, with the addition of R2O into CaO-Al2O3-B2O3 system, the number of bridging oxygen and the degree of polymerization of [AlO4] network were decreased. DSC results showed that the crystallization process became more sluggish with the increase of B2O3, which indicated that the crystallization ability was weakened. While the quenched mold fluxes crystallized more rapidly when introducing R2O. In other word, the crystallization rates of CaO-Al2O3 based slags were accelerated by the introduction of R2O. The liquidus temperature and crystallization temperature were decreased with the increasing amount of B2O3 or by addition of R2O into CaO-Al2O3 system. Only one kind of crystal was precipitated in 8% B2O3 and %R2O-containing samples, which was CaAl2O4 identified by SEM-EDS. When the content of B2O3 increased from 8% to 16%, Ca3B2O6 is clearly observed, demonstrating that the crystallization ability of Ca3B2O6 is enhanced by the increasing concentration of B2O3 in mold flux. The Ca/Al ratio of the generated calcium aluminate has been altered from 1:2 to 1:4 with the increasing of B2O3. The size of CaAl2O4 crystal is gradually increased with the addition of R2O. The crystallization ability of CaAl2O4 is promoted by R2O.

  11. High-accuracy determination of the neutron flux in the new experimental area n_TOF-EAR2 at CERN

    NASA Astrophysics Data System (ADS)

    Sabaté-Gilarte, M.; Barbagallo, M.; Colonna, N.; Gunsing, F.; Žugec, P.; Vlachoudis, V.; Chen, Y. H.; Stamatopoulos, A.; Lerendegui-Marco, J.; Cortés-Giraldo, M. A.; Villacorta, A.; Guerrero, C.; Damone, L.; Audouin, L.; Berthoumieux, E.; Cosentino, L.; Diakaki, M.; Finocchiaro, P.; Musumarra, A.; Papaevangelou, T.; Piscopo, M.; Tassan-Got, L.; Aberle, O.; Andrzejewski, J.; Bécares, V.; Bacak, M.; Baccomi, R.; Balibrea, J.; Barros, S.; Bečvář, F.; Beinrucker, C.; Belloni, F.; Billowes, J.; Bosnar, D.; Brugger, M.; Caamaño, M.; Calviño, F.; Calviani, M.; Cano-Ott, D.; Cardella, R.; Casanovas, A.; Castelluccio, D. M.; Cerutti, F.; Chiaveri, E.; Cortés, G.; Deo, K.; Domingo-Pardo, C.; Dressler, R.; Dupont, E.; Durán, I.; Fernández-Domínguez, B.; Ferrari, A.; Ferreira, P.; Frost, R. J. W.; Furman, V.; Göbel, K.; García, A. R.; Gawlik, A.; Gheorghe, I.; Glodariu, T.; Gonçalves, I. F.; González, E.; Goverdovski, A.; Griesmayer, E.; Harada, H.; Heftrich, T.; Heinitz, S.; Hernández-Prieto, A.; Heyse, J.; Jenkins, D. G.; Jericha, E.; Käppeler, F.; Kadi, Y.; Katabuchi, T.; Kavrigin, P.; Ketlerov, V.; Khryachkov, V.; Kimura, A.; Kivel, N.; Kokkoris, M.; Krtička, M.; Leal-Cidoncha, E.; Lederer, C.; Leeb, H.; Licata, M.; Lo Meo, S.; Lonsdale, S. J.; Losito, R.; Macina, D.; Marganiec, J.; Martínez, T.; Massimi, C.; Mastinu, P.; Mastromarco, M.; Matteucci, F.; Maugeri, E. A.; Mendoza, E.; Mengoni, A.; Milazzo, P. M.; Mingrone, F.; Mirea, M.; Montesano, S.; Nolte, R.; Oprea, A.; Palomo-Pinto, F. R.; Paradela, C.; Patronis, N.; Pavlik, A.; Perkowski, J.; Porras, J. I.; Praena, J.; Quesada, J. M.; Rajeev, K.; Rauscher, T.; Reifarth, R.; Riego-Perez, A.; Robles, M. S.; Rout, P. C.; Rubbia, C.; Ryan, J. A.; Saxena, A.; Schillebeeckx, P.; Schmidt, S.; Schumann, D.; Sedyshev, P.; Smith, A. G.; Suryanarayana, S. V.; Tagliente, G.; Tain, J. L.; Tarifeño-Saldivia, A.; Tsinganis, A.; Valenta, S.; Vannini, G.; Variale, V.; Vaz, P.; Ventura, A.; Vlastou, R.; Wallner, A.; Warren, S.; Weigand, M.; Wolf, C.; Woods, P. J.; Weiss, C.; Wright, T.

    2017-10-01

    A new high flux experimental area has recently become operational at the n_TOF facility at CERN. This new measuring station, n_TOF-EAR2, is placed at the end of a vertical beam line at a distance of approximately 20m from the spallation target. The characterization of the neutron beam, in terms of flux, spatial profile and resolution function, is of crucial importance for the feasibility study and data analysis of all measurements to be performed in the new area. In this paper, the measurement of the neutron flux, performed with different solid-state and gaseous detection systems, and using three neutron-converting reactions considered standard in different energy regions is reported. The results of the various measurements have been combined, yielding an evaluated neutron energy distribution in a wide energy range, from 2meV to 100MeV, with an accuracy ranging from 2%, at low energy, to 6% in the high-energy region. In addition, an absolute normalization of the n_TOF-EAR2 neutron flux has been obtained by means of an activation measurement performed with 197Au foils in the beam.

  12. Effects and mechanism of freeze-thawing cycles on the soil N2O fluxes in the temperate semi-arid steppe.

    PubMed

    Wang, Liqin; Qi, Yuchun; Dong, Yunshe; Peng, Qin; Guo, Shufang; He, Yunlong; Li, Zhaolin

    2017-06-01

    High nitrous oxide (N 2 O) emissions during freeze-thawing period (FTP) have been observed in many different ecosystems. However, the knowledge about the dynamic of soil N 2 O emissions and its main driving mechanism during the freeze-thawing processes in grassland ecosystem is still limited. An in-situ experiment was conducted during the FTP on the sites with 0 and 15% surplus of the average rainfall and two levels of N addition (0,10gN/(m 2 ·year)) during growing season (marked as W0N0, W15N0, W0N10, W15N10, respectively) to explore the effects of water and N background on soil N 2 O emissions during FTPs and the relationship between soil N 2 O emissions and environmental factors. The results indicated that water and N treatments conducted during growing season did not show significant effect on the N 2 O effluxes of FTP, but the soil mineral N contents of W0N10 treatment were significantly higher than those of W0N0, W15N0, W15N10 treatments (p<0.05). The soil PLFA concentrations of microbial groups monitored during 2015 spring freeze-thawing period (2015S-FTP) were lower than those during winter freeze-thawing period of 2014 (2014W-FTP), while cumulative soil N 2 O emissions of 2015S-FTP were higher than those of 2014W-FTP. The correlations between soil N 2 O effluxes and most of the measured environmental factors were insignificant, multiple stepwise regression analysis indicated that the soil temperature, soil NH 4 + -N content and air temperature were the major environmental factors which significantly influenced the N 2 O effluxes during 2014W-FTP, and air temperature and soil water content were the significant influencing factors during 2015S-FTP. Copyright © 2016. Published by Elsevier B.V.

  13. Stratospheric N2O5, CH4, and N2O profiles from IR solar occultation spectra

    NASA Technical Reports Server (NTRS)

    Camy-Peyret, C.; Flaud, J.-M.; Perrin, A.; Rinsland, C. P.; Goldman, A.; Murcray, F. J.

    1993-01-01

    Stratospheric volume mixing ratio profiles of N2O5, CH4, and N2O have been retrieved from a set of 0.052/cm resolution (FWHM) solar occultation spectra recorded at sunrise during a balloon flight from Aire sur l'Adour, France (44 N latitude) on 12 October 1990. The N2O5 results have been derived from measurements of the integrated absorption by the 1246/cm band. Assuming a total intensity of 4.32 x 10 exp -17 cm/molecule/sq cm independent of temperature, the retrieved N2O5 volume mixing ratios in ppbv, interpolated to 2 km height spacings, are 1.64 +/- 0.49 at 37.5 km, 1.92 +/- 0.56 at 35.5 km, 2.06 +/- 0.47 at 33.5 km, 1.95 +/- 0.42 at 31.5 km, 1.60 +/- 0.33 at 29.5 km, 1.26 +/- 0.28 at 27.5 km, and 0.85 +/- 0.20 at 25.5 km. Error bars indicate the estimated 1-sigma uncertainty including the error in the total band intensity. The retrieved profiles are compared with previous measurements and photochemical model results.

  14. Measurements of the O+ plus N2 and O+ plus O2 reaction rates from 300 to 900 K

    NASA Technical Reports Server (NTRS)

    Chen, A.; Johnsen, R.; Biondi, M. A.

    1977-01-01

    Rate coefficients for the O(+) + N2 atom transfer and O(+) + O2 charge transfer reactions are determined at thermal energies between 300 K and 900 K difference in a heated drift tube mass spectrometer apparatus. At 300 K the values K(O(+) + N2) = (1.2 plus or minus 0.1) x 10 to the negative 12 power cubic cm/sec and k(O(+) + O2) = (2.1 plus or minus 0.2) x 10 to the negative 11 power cubic cm/sec were obtained, with a 50% difference decrease in the reaction rates upon heating to 700 K. These results are in good agreement with heated flowing afterglow results, but the O(+) + O2 thermal rate coefficients are systematically lower than equivalent Maxwellian rates inferred by conversion of nonthermal drift tube and flow drift data.

  15. Valence band offset of β-Ga2O3/wurtzite GaN heterostructure measured by X-ray photoelectron spectroscopy

    PubMed Central

    2012-01-01

    A sample of the β-Ga2O3/wurtzite GaN heterostructure has been grown by dry thermal oxidation of GaN on a sapphire substrate. X-ray diffraction measurements show that the β-Ga2O3 layer was formed epitaxially on GaN. The valence band offset of the β-Ga2O3/wurtzite GaN heterostructure is measured by X-ray photoelectron spectroscopy. It is demonstrated that the valence band of the β-Ga2O3/GaN structure is 1.40 ± 0.08 eV. PMID:23046910

  16. Nitrous oxide fluxes from upland soils in central Hokkaido, Japan.

    PubMed

    Mu, Zhijian; Kimura, Sonoko D; Toma, Yo; Hatano, Ryusuke

    2008-01-01

    Nitrous oxide (N2O) fluxes from soils were measured using the closed chamber method during the snow-free seasons (middle April to early November), for three years, in a total of 11 upland crop fields in central Hokkaido, Japan. The annual mean N2O fluxes ranged from 2.95 to 164.17 microgN/(m2 x h), with the lowest observed in a grassland and the highest in an onion field. The instantaneous N2O fluxes showed a large temporal variation with peak emissions generally occurring following fertilization and heavy rainfall events around harvesting in autumn. No clear common factor regulating instantaneous N2O fluxes was found at any of the study sites. Instead, instantaneous N2O fluxes at different sites were affected by different soil variables. The cumulative N2O emissions during the study period within each year varied from 0.15 to 7.05 kgN/hm2 for different sites, which accounted for 0.33% to 5.09% of the applied fertilizer N. No obvious relationship was observed between cumulative N2O emission and applied fertilizer N rate (P > 0.4). However, the cumulative N2O emission was significantly correlated with gross mineralized N as estimated by CO2 emissions from bare soils divided by C/N ratios of each soil, and with soil mineral N pool (i.e., the sum of gross mineralized N and fertilizer N) (P < 0.001).

  17. Low Temperature Flux Growth of 2H-SiC and Beta-Gallium Oxide

    NASA Technical Reports Server (NTRS)

    Singh, N. B.; Choa, Fow-Sen; Su, Ching-Hua; Arnold, Bradley; Kelly, Lisa

    2016-01-01

    We present brief overview of our study on the low temperature flux growth of two very important novel wide bandgap materials 2H-SiC and Beta-gallium oxide (Beta-Ga2O3). We have synthesized and grown 5 millimeter to 1 centimeter size single crystals of Beta-gallium oxide (Beta-Ga2O3). We used a flux and semi wet method to grow transparent good quality crystals. In the semi-wet method Ga2O3 was synthesized with starting gallium nitrate solution and urea as a nucleation agent. In the flux method we used tin and other metallic flux. This crystal was placed in an alumina crucible and temperature was raised above 1050 degrees Centigrade. After a time period of thirty hours, we observed prismatic and needle shaped crystals of gallium oxide. Scanning electron microscopic studies showed step growth morphology. Crystal was polished to measure the properties. Bandgap was measured 4.7electronvolts using the optical absorption curve. Another wide bandgap hexagonal 2H-SiC was grown by using Si-Al eutectic flux in the graphite crucible. We used slight AlN also as the impurity in the flux. The temperature was raised up to 1050 degrees Centigrade and slowly cooled to 850 degrees Centigrade. Preliminary characterization results of this material are also reported.

  18. Seasonal effect on N2O formation in nitrification in constructed wetlands.

    PubMed

    Inamori, Ryuhei; Wang, Yanhua; Yamamoto, Tomoko; Zhang, Jixiang; Kong, Hainan; Xu, Kaiqin; Inamori, Yuhei

    2008-10-01

    Constructed wetlands are considered to be important sources of nitrous oxide (N(2)O). In order to investigate the contribution of nitrification in N(2)O formation, some environmental factors, plant species and ammonia-oxidizing bacteria (AOB) in active layers have been compared. Vegetation cells indicated remarkable effect of seasons and different plant species on N(2)O emission and AOB amount. Nitrous oxide data showed large temporal and spatial fluctuations ranging 0-52.8 mg N(2)O m(-2)d(-1). Higher AOB amount and N(2)O flux rate were observed in the Zizania latifolia cell, reflecting high potential of global warming. Roles of plants as ecosystem engineers are summarized with rhizosphere oxygen release and organic matter transportation to affect nitrogen transformation. The Phragmites australis cell contributed to keeping high T-N removal performance and lower N(2)O emission. The distribution of AOB also supported this result. Statistical analysis showed several environmental parameters affecting the strength of observed greenhouse gases emission, such as water temperature, water level, TOC, plant species and plant cover.

  19. Photocatalytic decomposition of N2O over TiO2/g-C3N4 photocatalysts heterojunction

    NASA Astrophysics Data System (ADS)

    Kočí, K.; Reli, M.; Troppová, I.; Šihor, M.; Kupková, J.; Kustrowski, P.; Praus, P.

    2017-02-01

    TiO2/g-C3N4 photocatalysts with the various TiO2/g-C3N4 weight ratios from 1:2 to 1:6 were fabricated by mechanical mixing in water suspension followed by calcination. Pure TiO2 was prepared by thermal hydrolysis and pure g-C3N4 was prepared from commercial melamine by thermal annealing at 620 °C. All the nanocomposites were characterized by X-ray powder diffraction, UV-vis diffuse reflectance spectroscopy, Raman spectroscopy, infrared spectroscopy, scanning electron microscopy, transmission electron microscopy, photoelectrochemical measurements and nitrogen physisorption. The prepared mixtures along with pure TiO2 and g-C3N4 were tested for the photocatalytic decomposition of nitrous oxide under UVC (λ = 254 nm), UVA (λ = 365 nm) and Vis (λ > 400 nm) irradiation. The TiO2/g-C3N4 nanocomposites showed moderate improvement compared to pure g-C3N4 but pure TiO2 proved to be a better photocatalyst under UVC irradiation. However, under UVA irradiation conditions, the photocatalytic activity of TiO2/g-C3N4 (1:2) nanocomposite exhibited an increase compared to pure TiO2. Nevertheless, further increase of g-C3N4 amount leads/led to a decrease in reactivity. These results are suggesting the nanocomposite with the optimal weight ratio of TiO2 and g-C3N4 have shifted absorption edge energy towards longer wavelengths and decreased the recombination rate of charge carriers compared to pure g-C3N4. This is probably due to the generation of heterojunction on the TiO2/g-C3N4 interface.

  20. Top-down constraints on global N2O emissions at optimal resolution: application of a new dimension reduction technique

    NASA Astrophysics Data System (ADS)

    Wells, Kelley C.; Millet, Dylan B.; Bousserez, Nicolas; Henze, Daven K.; Griffis, Timothy J.; Chaliyakunnel, Sreelekha; Dlugokencky, Edward J.; Saikawa, Eri; Xiang, Gao; Prinn, Ronald G.; O'Doherty, Simon; Young, Dickon; Weiss, Ray F.; Dutton, Geoff S.; Elkins, James W.; Krummel, Paul B.; Langenfelds, Ray; Steele, L. Paul

    2018-01-01

    We present top-down constraints on global monthly N2O emissions for 2011 from a multi-inversion approach and an ensemble of surface observations. The inversions employ the GEOS-Chem adjoint and an array of aggregation strategies to test how well current observations can constrain the spatial distribution of global N2O emissions. The strategies include (1) a standard 4D-Var inversion at native model resolution (4° × 5°), (2) an inversion for six continental and three ocean regions, and (3) a fast 4D-Var inversion based on a novel dimension reduction technique employing randomized singular value decomposition (SVD). The optimized global flux ranges from 15.9 Tg N yr-1 (SVD-based inversion) to 17.5-17.7 Tg N yr-1 (continental-scale, standard 4D-Var inversions), with the former better capturing the extratropical N2O background measured during the HIAPER Pole-to-Pole Observations (HIPPO) airborne campaigns. We find that the tropics provide a greater contribution to the global N2O flux than is predicted by the prior bottom-up inventories, likely due to underestimated agricultural and oceanic emissions. We infer an overestimate of natural soil emissions in the extratropics and find that predicted emissions are seasonally biased in northern midlatitudes. Here, optimized fluxes exhibit a springtime peak consistent with the timing of spring fertilizer and manure application, soil thawing, and elevated soil moisture. Finally, the inversions reveal a major emission underestimate in the US Corn Belt in the bottom-up inventory used here. We extensively test the impact of initial conditions on the analysis and recommend formally optimizing the initial N2O distribution to avoid biasing the inferred fluxes. We find that the SVD-based approach provides a powerful framework for deriving emission information from N2O observations: by defining the optimal resolution of the solution based on the information content of the inversion, it provides spatial information that is lost when

  1. In situ stratospheric measurements of CH4, (C-13)H4, N2O, and OC(O-18) using the BLISS tunable diode laser spectrometer

    NASA Technical Reports Server (NTRS)

    Webster, Christopher R.; May, Randy D.

    1992-01-01

    Simultaneous in situ measurements of stratospheric CH4, (C-13)H4, N2O, OC(O-18), pressure, and temperature have been made from Palestine, Texas (32 deg N) in September 1988 with the JPL Balloon-borne Laser In Situ Sensor. Measurements of CH4 and N2O in the altitude range 30-35 km agree well with other measurements, except for an anomalously high value for the N2O at 31 km. Measurements of CH4 support earlier observations of fold in the vertical profile. A ratio for stratospheric (C-13)H4/CH4 of 0.0105 +/- 0.0010 implies an enrichment of delta(C-13) = -45 +/- 92 parts per thousand over the PDB value, in agreement with previous measurements in the troposphere. A large mixing ratio of 1.9 +/- 0.2 ppmv for OC(O-18) is measured, corresponding to an enrichment of delta(O-18) = 280 +/- 50 parts per thousand for the (O-18) isotopic species over the SMOW value.

  2. Aquatic Eddy Correlation: Quantifying the Artificial Flux Caused by Stirring-Sensitive O2 Sensors

    PubMed Central

    Holtappels, Moritz; Noss, Christian; Hancke, Kasper; Cathalot, Cecile; McGinnis, Daniel F.; Lorke, Andreas; Glud, Ronnie N.

    2015-01-01

    In the last decade, the aquatic eddy correlation (EC) technique has proven to be a powerful approach for non-invasive measurements of oxygen fluxes across the sediment water interface. Fundamental to the EC approach is the correlation of turbulent velocity and oxygen concentration fluctuations measured with high frequencies in the same sampling volume. Oxygen concentrations are commonly measured with fast responding electrochemical microsensors. However, due to their own oxygen consumption, electrochemical microsensors are sensitive to changes of the diffusive boundary layer surrounding the probe and thus to changes in the ambient flow velocity. The so-called stirring sensitivity of microsensors constitutes an inherent correlation of flow velocity and oxygen sensing and thus an artificial flux which can confound the benthic flux determination. To assess the artificial flux we measured the correlation between the turbulent flow velocity and the signal of oxygen microsensors in a sealed annular flume without any oxygen sinks and sources. Experiments revealed significant correlations, even for sensors designed to have low stirring sensitivities of ~0.7%. The artificial fluxes depended on ambient flow conditions and, counter intuitively, increased at higher velocities because of the nonlinear contribution of turbulent velocity fluctuations. The measured artificial fluxes ranged from 2 - 70 mmol m-2 d-1 for weak and very strong turbulent flow, respectively. Further, the stirring sensitivity depended on the sensor orientation towards the flow. For a sensor orientation typically used in field studies, the artificial flux could be predicted using a simplified mathematical model. Optical microsensors (optodes) that should not exhibit a stirring sensitivity were tested in parallel and did not show any significant correlation between O2 signals and turbulent flow. In conclusion, EC data obtained with electrochemical sensors can be affected by artificial flux and we recommend

  3. Subsurface watering resulted in reduced soil N2O and CO2 emissions and their global warming potentials than surface watering

    NASA Astrophysics Data System (ADS)

    Wei, Qi; Xu, Junzeng; Yang, Shihong; Liao, Linxian; Jin, Guangqiu; Li, Yawei; Hameed, Fazli

    2018-01-01

    Water management is an important practice with significant effect on greenhouse gases (GHG) emission from soils. Nitrous oxide (N2O) and carbon dioxide (CO2) emissions and their global warming potentials (GWPs) from subsurface watering soil (SUW) were investigated, with surface watering (SW) as a control. Results indicated that the N2O and CO2 emissions from SUW soils were somewhat different to those from SW soil, with the peak N2O and CO2 fluxes from SUW soil reduced by 28.9% and 19.4%, and appeared 72 h and 168 h later compared with SW. The fluxes of N2O and CO2 from SUW soils were lower than those from SW soil in both pulse and post-pulse periods, and the reduction was significantly (p<0.05) in pulse period. Compare to SW, the cumulative N2O and CO2 emissions and its integrative GWPs from SUW soil decreased by 21.0% (p<0.05), 15.9% and 18.0%, respectively. The contributions of N2O to GWPs were lower than those of CO2 during most of time, except in pulse emission periods, and the proportion of N2O from SUW soil was 1.4% (p>0.1) lower that from SW soil. Moreover, N2O and CO2 fluxes from both watering treatments increased exponentially with increase of soil water-filled pore space (WFPS) and temperature. Our results suggest that watering soil from subsurface could significantly reduce the integrative greenhouse effect caused by N2O and CO2 and is a promising strategy for soil greenhouse gases (GHGs) mitigation. And the pulse period, contributed most to the reduction in emissions of N2O and CO2 from soils between SW and SUW, should be a key period for mitigating GHGs emissions. Response of N2O and CO2 emissions to soil WFPS and temperature illustrated that moisture was the dominant parameters that triggering GHG pulse emissions (especially for N2O), and temperature had a greater effect on the soil microorganism activity than moisture in drier soil. Avoiding moisture and temperature are appropriate for GHG emission at the same time is essential for GHGs mitigation

  4. Comparison of Source Partitioning Methods for CO2 and H2O Fluxes Based on High Frequency Eddy Covariance Data

    NASA Astrophysics Data System (ADS)

    Klosterhalfen, Anne; Moene, Arnold; Schmidt, Marius; Ney, Patrizia; Graf, Alexander

    2017-04-01

    Source partitioning of eddy covariance (EC) measurements of CO2 into respiration and photosynthesis is routinely used for a better understanding of the exchange of greenhouse gases, especially between terrestrial ecosystems and the atmosphere. The most frequently used methods are usually based either on relations of fluxes to environmental drivers or on chamber measurements. However, they often depend strongly on assumptions or invasive measurements and do usually not offer partitioning estimates for latent heat fluxes into evaporation and transpiration. SCANLON and SAHU (2008) and SCANLON and KUSTAS (2010) proposed an promising method to estimate the contributions of transpiration and evaporation using measured high frequency time series of CO2 and H2O fluxes - no extra instrumentation necessary. This method (SK10 in the following) is based on the spatial separation and relative strength of sources and sinks of CO2 and water vapor among the sub-canopy and canopy. Assuming that air from those sources and sinks is not yet perfectly mixed before reaching EC sensors, partitioning is estimated based on the separate application of the flux-variance similarity theory to the stomatal and non-stomatal components of the regarded fluxes, as well as on additional assumptions on stomatal water use efficiency (WUE). The CO2 partitioning method after THOMAS et al. (2008) (TH08 in the following) also follows the argument that the dissimilarities of sources and sinks in and below a canopy affect the relation between H2O and CO2 fluctuations. Instead of involving assumptions on WUE, TH08 directly screens their scattergram for signals of joint respiration and evaporation events and applies a conditional sampling methodology. In spite of their different main targets (H2O vs. CO2), both methods can yield partitioning estimates on both fluxes. We therefore compare various sub-methods of SK10 and TH08 including own modifications (e.g., cluster analysis) to each other, to established

  5. Linking N2O emission from biochar-amended composting process to the abundance of denitrify (nirK and nosZ) bacteria community.

    PubMed

    Li, Shuqing; Song, Lina; Jin, Yaguo; Liu, Shuwei; Shen, Qirong; Zou, Jianwen

    2016-12-01

    Manure composting has been recognized as an important anthropogenic source of nitrous oxide (N2O) contributing to global warming. However, biochar effect on N2O emissions from manure composting is rarely evaluated, especially by linking it to abundance of denitrifying bacteria community. Results of this study indicated that biochar amendment significantly reduced N2O emissions from manure composting, primarily due to suppression of the nirK gene abundance of denitrifying bacteria. Pearson's correlation analysis showed a significant positive correlation between nirK abundance and N2O fluxes, while a negative correlation between nosZ density and N2O fluxes. Simultaneously, a linear correlation between nirK gene abundance minus nosZ gene abundance with N2O fluxes was also observed. In addition, a statistical model for estimating N2O emissions based on the bacterial denitrifying functional genes was developed and verified to adequately fit the observed emissions. Our results highlighted that biochar amendment would be an alternative strategy for mitigating N2O emissions during manure composting, and the information of related functional bacterial communities could be helpful for understanding the mechanism of N2O emissions.

  6. Stratospheric N2O5, CH4, and N2O Profiles from IR Solar Occultation Spectra

    NASA Technical Reports Server (NTRS)

    Peyeret, C. Camy; Flaud, J.-M.; Perrin, A.; Rinsland, C. P.; Goldman, A.; Murcray, F. J.

    1993-01-01

    Stratospheric volume mixing ratio profiles of N2O5, CH4, and N2O have been retrieved from a set of 0.052/ cm resolution (FWHM) solar occultation spectra recorded at sunrise during a balloon flight from Aire sur I'Adour, France (44 deg N latitude) on 12 October 1990. The N2O5 results have been derived from measurements of the integrated absorption by the 1246/ cm band. Assuming a total intensity of 4.32 x 10(exp 17)cm(exp -1) molecule sq cm(exp -2) independent of temperature, the retrieved N2O5 volume mixing ratios in ppbv (parts per billion by volume, 10(exp -9)), interpolated to 2 km height spacings, are 1.64 +/- 0.49 at 37.5 km, 1.92 +/- 0.56 at 35.5 km, 2.06 +/- 0.47 at 33.5 km, 1.95 +/- 0.42 at 31.5 km, 1.60 +/- 0.33 at 29.5 km, 1.26 +/- 0.28 at 27.5 km, and 0.85 +/- 0.20 at 25.5 km. Error bars indicate the estimated I-sigma uncertainty including the error in the total band intensity (+/- 20% has been assumed). The retrieved profiles are compared with previous measurements and photochemical model results.

  7. Influence of aerosol chemical composition on N2O5 uptake: airborne regional measurements in North-Western Europe

    NASA Astrophysics Data System (ADS)

    Morgan, W. T.; Ouyang, B.; Allan, J. D.; Aruffo, E.; Di Carlo, P.; Kennedy, O. J.; Lowe, D.; Flynn, M. J.; Rosenberg, P. D.; Williams, P. I.; Jones, R.; McFiggans, G. B.; Coe, H.

    2014-07-01

    Aerosol chemical composition was found to influence nighttime atmospheric chemistry during a series of airborne measurements in North-Western Europe in summer conditions, which has implications for regional air quality and climate. The uptake of dinitrogen pentoxide, γ (N2O5), to particle surfaces was found to be modulated by the amount of water content and ammonium nitrate present in the aerosol. The conditions prevalent in this study suggest that the net uptake rate of N2O5 to atmospheric aerosols was relatively efficient compared to previous studies, with γ (N2O5) values in the range 0.01-0.03. This is likely a consequence of the elevated relative humidity in the region, which promotes greater aerosol water content. Increased nitrate concentrations relative to particulate water were found to suppress N2O5 uptake. The results presented here contrast with previous ambient studies of N2O5 uptake, which have generally taken place in low-nitrate environments in the USA. Comparison of the N2O5 uptake derived from the measurements with a parameterised scheme that is based on the ratio of particulate water to nitrate yielded reasonably good agreement in terms of the magnitude and variation in uptake, provided the effect of chloride was neglected. An additional suppression of the parameterised uptake is likely required to fully capture the variation in N2O5 uptake, which could be achieved via the known suppression by organic aerosol. However, existing parameterisations representing the suppression by organic aerosol were unable to fully represent the variation in N2O5 uptake. These results provide important ambient measurement constraint on our ability to predict N2O5 uptake in regional and global aerosol models. N2O5 uptake is a potentially important source of nitrate aerosol and a sink of the nitrate radical, which is the main nocturnal oxidant in the atmosphere. The results further highlight the importance of ammonium nitrate in North-Western Europe as a key

  8. Crystallization Behavior and Heat Transfer of Fluorine-Free Mold Fluxes with Different Na2O Concentration

    NASA Astrophysics Data System (ADS)

    Yang, Jian; Zhang, Jianqiang; Sasaki, Yasushi; Ostrovski, Oleg; Zhang, Chen; Cai, Dexiang; Kashiwaya, Yoshiaki

    2016-08-01

    In this study, the crystallization behavior and heat transfer of CaO-SiO2-Na2O-B2O3-TiO2-Al2O3-MgO-Li2O fluorine-free mold fluxes with different Na2O contents (5 to 11 mass pct) were studied using single/double hot thermocouple technique (SHTT/DHTT) and infrared emitter technique (IET), respectively. Continuous cooling transformation (CCT) and time-temperature transformation (TTT) diagrams constructed using SHTT showed that crystallization temperature increased and incubation time shortened with the increase of Na2O concentration, indicating an enhanced crystallization tendency. The crystallization process of mold fluxes in the temperature field simulating the casting condition was also investigated using DHTT. X-ray diffraction (XRD) analysis of the quenched mold fluxes showed that the dominant phase changed from CaSiO3 to Ca11Si4B2O22 with the increasing concentration of Na2O. The heat transfer examined by IET showed that the increase of Na2O concentration reduced the responding heat flux when Na2O was lower than 9 mass pct but the further increase of Na2O to 11 mass pct enhanced the heat flux. The correlation between crystallinity and heat transfer was discussed in terms of crystallization tendency and crystal morphology.

  9. Solution for Minimizing Surface Heating Effect for Fast Open-Path CO2 Flux Measurements in Cold Environments

    NASA Astrophysics Data System (ADS)

    Hupp, J. R.; Burba, G. G.; McDermitt, D. K.; Anderson, D. J.; Eckles, R. D.

    2010-12-01

    Open-path design of the high speed gas analyzers is a well-established configuration widely used for measurements of CO2 fluxes and concentrations. This configuration has advantages and deficiencies. Advantages include excellent frequency response, long-term stability, low sensitivity to window contamination, low-power pump-free operation, and infrequent calibration requirements. Deficiencies include susceptibility to precipitation and icing, and a potential need for instrument surface heating correction in extremely cold environments. In spite of the deficiencies, open-path measurements often provide data coverage that would not have been possible using traditional closed-path approach. Data loss from precipitation and icing may not always be prevented for the open-path instruments, while heating effect does not pose a problem for CO2 flux in warm environments. Even in cold environments, the impact of heating on CO2 flux is much smaller than other well-known effects, such as Webb-Pearman-Leuning terms, or frequency response corrections for closed-path analyzers. Nonetheless, instrument surface heating effect in cold environments could be addressed scientifically, via developing the theoretical corrections, and instrumentally, via measuring fast integrated air temperature in the optical path, or via enclosing the open-path instrument into a low-power short-intake design. Here we provide an alternative way to minimize or eliminate open-path heating effect, achieved by minimizing or eliminating the temperature gradient between the instrument surface and ambient air. Open-path low temperature controlled design is discussed in comparison with two other approaches (e.g., traditional open-path design and closed-path design) in terms of their field performance for Eddy Covariance flux measurements in the cold. This study presents field data from a new open-path CO2/H2O gas analyzer, LI-7500A, based on the LI-7500 model modified to produce substantially less heat during

  10. [Effects of organic and inorganic fertilizers on emission and sources of N2O in vegetable soils.

    PubMed

    Lin, Wei; Ding, Jun Jun; Li, Yu Zhong; Xu, Chun Ying; Li, Qiao Zhen; Zheng, Qian; Zhuang, Shan

    2018-05-01

    To clarify the microbial pathway of the N 2 O production and consumption under different fertilizers and provide theoretical basis for the reduction of N 2 O emission and rational management of fertilization in vegetable soils, we examined dynamics of N 2 O flux and isotope signatures under different fertilizer treatments in the vegetable soils of Beijing, by setting up four treatments (organic-acetylene, organic-nonacetylene, inorganic-acetylene, inorganic-nonacetylene) and using the stable isotope technique of natural N 2 O abundance. The results showed that the cumulative N 2 O emission from organic-acetylene group, organic-nonacetylene group, inorganic-acetylene group and inorganic-nonacetylene group was (374±37), (283±34), (458±36), (355±41) g·m -2 in cabbage growing season, respectively. N 2 O fluxes were significantly lower in treatments with organic fertilizer than those with inorganic fertilizer and significantly higher in acetylene group than nonacetylene group. The degree of N 2 O reduction were similar in both fertilizer treatments, and higher nitrification was found in inorganic fertilizer than organic fertilizer treatments. Acetylene only inhibited partial nitrification and partial N 2 O reduction at the peak of N 2 O emission. When the emission was reduced, N 2 O reduction could be completely suppressed. Therefore, the inorganic fertilizer might trigger nitrification and promote higher N 2 O emission. The high concentration of N 2 O could withstand that acetylene to inhibite N 2 O reduction. Hence, using organic fertilizers instead of some inorganic ones could effectively reduce N 2 O emission in vegetable soils of Beijing. The N 2 O concentration threshold should be considered when we identify N 2 O source by acetylene inhibition method.

  11. Non-growing season nitrous oxide fluxes from agricultural soils

    NASA Astrophysics Data System (ADS)

    Kariyapperuma Athukoralage, Kumudinie

    A two-year field experiment was conducted at the Arkell Research Station, Ontario, Canada to evaluate composting as a mitigation strategy for greenhouse gases (GHGs). The objectives were to quantify and compare non-growing season nitrous oxide (N2O) fluxes from agricultural soils after fall manure application of composted and untreated liquid swine manure. Nitrous oxide fluxes were measured using a micrometeorological method. Compared to untreated liquid swine manure (LSM), composted swine manure (CSM) resulted in 57% reduction of soil N2O emissions during February to April in 2005, but emissions during the same period in 2006 were not affected by treatments. This effect was related to fall and winter weather conditions with the significant reduction occurring in the year when soil freezing was more pronounced. The DNDC (DeNitrification-DeComposition) model was tested against data measured during the non-growing seasons from 2000 to 2004, for farming with conventional management at the Elora Research Station, Ontario, Canada. The objective was to assess the ability of the DNDC model to simulate non-growing season N2O fluxes from soils in southwestern Ontario. Comparison between model-simulated and measured data indicated that background fluxes were relatively well predicted. The spring thaw N2O flux event was correctly timed by the DNDC model, but was smaller than the measured spring thaw event. Though there was no N2O emission event measured in early May, the DNDC model predicted a large event, simultaneous with the physical release of predicted ice-trapped N2O. Removing the large and late predicted emission peak and increasing the contribution of newly produced N2O due to denitrification to the early spring thaw event were proposed. Three data sets from studies conducted in Ontario, Canada were used to estimate and compare the overall GHG (N2O and methane) emissions from LSM and CSM. Compared to LSM storage, the composting process reduced GHG emissions by 35% (CO

  12. Full GHG balance of a drained fen peatland cropped to spring barley and reed canary grass using comparative assessment of CO2 fluxes.

    PubMed

    Karki, Sandhya; Elsgaard, Lars; Kandel, Tanka P; Lærke, Poul Erik

    2015-03-01

    Empirical greenhouse gas (GHG) flux estimates from diverse peatlands are required in order to derive emission factors for managed peatlands. This study on a drained fen peatland quantified the annual GHG balance (Carbon dioxide (CO2), nitrous oxide (N2O), methane (CH4), and C exported in crop yield) from spring barley (SB) and reed canary grass (RCG) using static opaque chambers for GHG flux measurements and biomass yield for indirectly estimating gross primary production (GPP). Estimates of ecosystem respiration (ER) and GPP were compared with more advanced but costly and labor-intensive dynamic chamber studies. Annual GHG balance for the two cropping systems was 4.0 ± 0.7 and 8.1 ± 0.2 Mg CO2-Ceq ha(-1) from SB and RCG, respectively (mean ± standard error, n = 3). Annual CH4 emissions were negligible (<0.006 Mg CO2-Ceq ha(-1)), and N2O emissions contributed only 4-13 % of the full GHG balance (0.5 and 0.3 Mg CO2-Ceq ha(-1) for SB and RCG, respectively). The statistical significance of low CH4 and N2O fluxes was evaluated by a simulation procedure which showed that most of CH4 fluxes were within the range that could arise from random variation associated with actual zero-flux situations. ER measured by static chamber and dynamic chamber methods was similar, particularly when using nonlinear regression techniques for flux calculations. A comparison of GPP derived from aboveground biomass and from measuring net ecosystem exchange (NEE) showed that GPP estimation from biomass might be useful, or serve as validation, for more advanced flux measurement methods. In conclusion, combining static opaque chambers for measuring ER of CO2 and CH4 and N2O fluxes with biomass yield for GPP estimation worked well in the drained fen peatland cropped to SB and RCG and presented a valid alternative to estimating the full GHG balance by dynamic chambers.

  13. Quantifying N2O emissions and production pathways from fresh waste during the initial stage of disposal to a landfill.

    PubMed

    Wang, Xiaojun; Jia, Mingsheng; Zhang, Han; Pan, Songqing; Kao, Chih Ming; Chen, Shaohua

    2017-05-01

    Intensive nitrous oxide (N 2 O) emissions usually occur at the working face of landfills. However, the specific amounts and contributions of the multiple pathways to N 2 O emissions are poorly understood. N 2 O emissions and the mutual conversions of N-species in both open and sealed simulated landfill reactors filled with fresh refuse were examined during a 100-h incubation period, and N 2 O sources were calculated using 15 N isotope labelling. N 2 O peak fluxes were above 70μgNkg -1 waste h -1 for both treatments. The sealed incubation reactors became a N 2 O sink when N 2 O in the ambient environment was sufficient. The total amount of N 2 O emissions under sealed conditions was 2.15±0.56mgNkg -1 waste, which was higher than that under open conditions (1.91±0.34mgNkg -1 waste). The NO 2 - peak appeared prior to the peak in N 2 O flux. The degree and duration of total nitrogen reduction in open incubations were larger and longer than those of sealed incubations and could possibly be due to oxygen supplementation. Denitrification (DF) was a major source of N 2 O generation during these incubations. The contribution of the DF pathway decreased from 89.2% to 61.3% during the open incubations. The effects of nitrification (NF) and nitrification-coupled denitrification (NCD) increased during the increasing phase and the decreasing phase of N 2 O flux, contributing 24.1-37.4% and 31.7-34.4% of total N 2 O emissions, respectively. In sealed treatments, the DF pathway accounted for more than 90% of the total N 2 O emission during the entire incubation. Copyright © 2016 Elsevier Ltd. All rights reserved.

  14. Methane and CO2 fluxes of moving point sources - Beyond or within the limits of eddy covariance measurements

    NASA Astrophysics Data System (ADS)

    Felber, Raphael; Neftel, Albrecht; Münger, Andreas; Ammann, Christof

    2014-05-01

    The eddy covariance (EC) technique has been extensively used for CO2 and energy exchange measurements over different ecosystems. For some years, it has been also becoming widely used to investigate CH4 and N2O exchange over ecosystems including grazing systems. EC measurements represent a spatially integrated flux over an upwind area (footprint). Whereas for extended homogenous areas EC measurements work well, the animals in a grazing system are a challenge as they represent moving point sources that create inhomogeneous conditions in space and time. The main issues which have to be taken into account when applying EC flux measurements over a grazed system are: i) In the presence of animals the high time resolution concentration measurements show large spikes in the signal. These spikes may be filtered/reduced by standard quality control software in order to avoid wrong measurements. ii) Data on the position of the animals relative to the flux footprint is needed to quantify the contribution of the grazing animals to the measured flux. For one grazing season we investigated the ability of EC flux measurements to reliably quantify the contribution of the grazing animals to the CH4 and CO2 exchange over pasture systems. For this purpose, a field experiment with a herd of twenty dairy cows in a full-day rotational grazing system was carried out on the Swiss central plateau. Net CH4 and CO2 exchange of the pasture system was measured continuously by the eddy covariance technique (Sonic Anemometer HS-50, Gill Instruments Ltd; FGGA, Los Gatos Research Inc.). To quantify the contribution of the animals to the net flux, the position of the individual cows was recorded using GPS (5 s time resolution) on each animal. An existing footprint calculation tool (ART footprint tool) was adapted and CH4 emissions of the cows were calculated. CH4 emissions from cows could be used as a tracer to investigate the quality of the evaluation of the EC data, since the background exchange of

  15. Oceanic N2O emissions in the 21st century

    NASA Astrophysics Data System (ADS)

    Martinez-Rey, J.; Bopp, L.; Gehlen, M.; Tagliabue, A.; Gruber, N.

    2014-12-01

    The ocean is a substantial source of nitrous oxide (N2O) to the atmosphere, but little is known on how this flux might change in the future. Here, we investigate the potential evolution of marine N2O emissions in the 21st century in response to anthropogenic climate change using the global ocean biogeochemical model NEMO-PISCES. We implemented two different parameterizations of N2O production, which differ primarily at low oxygen (O2) conditions. When forced with output from a climate model simulation run under the business-as-usual high CO2 concentration scenario (RCP8.5), our simulations suggest a decrease of 4 to 12% in N2O emissions from 2005 to 2100, i.e., a reduction from 4.03/3.71 to 3.54/3.56 Tg N yr-1 depending on the parameterization. The emissions decrease strongly in the western basins of the Pacific and Atlantic oceans, while they tend to increase above the Oxygen Minimum Zones (OMZs), i.e., in the Eastern Tropical Pacific and in the northern Indian Ocean. The reduction in N2O emissions is caused on the one hand by weakened nitrification as a consequence of reduced primary and export production, and on the other hand by stronger vertical stratification, which reduces the transport of N2O from the ocean interior to the ocean surface. The higher emissions over the OMZ are linked to an expansion of these zones under global warming, which leads to increased N2O production associated primarily with denitrification. From the perspective of a global climate system, the averaged feedback strength associated with the projected decrease in oceanic N2O emissions amounts to around -0.009 W m-2 K-1, which is comparable to the potential increase from terrestrial N2O sources. However, the assesment for a compensation between the terrestrial and marine feedbacks calls for an improved representation of N2O production terms in fully coupled next generation of Earth System Models.

  16. Permafrost collapse shifts alpine tundra to a carbon source but reduces N2O and CH4 release on the northern Qinghai-Tibetan Plateau

    NASA Astrophysics Data System (ADS)

    Mu, C.

    2017-12-01

    Important unknowns remain about how abrupt permafrost collapse (thermokarst) affects carbon balance and greenhouse gas flux, limiting our ability to predict the magnitude and timing of the permafrost carbon feedback. We measured monthly, growing-season fluxes of CO2, CH4, and N2O at a large thermokarst feature in alpine tundra on the northern Qinghai-Tibetan Plateau (QTP). Thermokarst formation disrupted plant growth and soil hydrology, shifting the ecosystem from a growing-season carbon sink to a weak source, but decreasing feature-level CH4 and N2O flux. Temperature-corrected ecosystem respiration from decomposing permafrost soil was 2.7 to 9.5-fold higher than in similar features from Arctic and Boreal regions, suggesting that warmer and dryer conditions on the northern QTP could accelerate carbon decomposition following permafrost collapse. N2O flux was similar to the highest values reported for Arctic ecosystems, and was 60% higher from exposed mineral soil on the feature floor, confirming Arctic observations of coupled nitrification and denitrification in collapsed soils. Q10 values for respiration were typically over 4, suggesting high temperature sensitivity of thawed carbon. Taken together, these results suggest that QTP permafrost carbon in alpine tundra is highly vulnerable to mineralization following thaw, and that N2O production could be an important non-carbon permafrost climate feedback.

  17. Development of a field-deployable method for simultaneous, real-time measurements of the four most abundant N2O isotopocules.

    PubMed

    Ibraim, Erkan; Harris, Eliza; Eyer, Simon; Tuzson, Béla; Emmenegger, Lukas; Six, Johan; Mohn, Joachim

    2018-03-01

    Understanding and quantifying the biogeochemical cycle of N 2 O is essential to develop effective N 2 O emission mitigation strategies. This study presents a novel, fully automated measurement technique that allows simultaneous, high-precision quantification of the four main N 2 O isotopocules ( 14 N 14 N 16 O, 14 N 15 N 16 O, 15 N 14 N 16 O and 14 N 14 N 18 O) in ambient air. The instrumentation consists of a trace gas extractor (TREX) coupled to a quantum cascade laser absorption spectrometer, designed for autonomous operation at remote measurement sites. The main advantages this system has over its predecessors are a compact spectrometer design with improved temperature control and a more compact and powerful TREX device. The adopted TREX device enhances the flexibility of the preconcentration technique for higher adsorption volumes to target rare isotope species and lower adsorption temperatures for highly volatile substances. All system components have been integrated into a standardized instrument rack to improve portability and accessibility for maintenance. With an average sampling frequency of approximately 1 h -1 , this instrumentation achieves a repeatability of 0.09, 0.13, 0.17 and 0.12 ‰ for δ 15 N α , δ 15 N β , δ 18 O and site preference of N 2 O, respectively, for pressurized ambient air. The repeatability for N 2 O mole fraction measurements is better than 1 ppb (parts per billion, 10 -9 moles per mole of dry air).

  18. Effects of crop management, soil type, and climate on N2O emissions from Austrian Soils

    NASA Astrophysics Data System (ADS)

    Zechmeister-Boltenstern, Sophie; Sigmund, Elisabeth; Kasper, Martina; Kitzler, Barbara; Haas, Edwin; Wandl, Michael; Strauss, Peter; Poetzelsberger, Elisabeth; Dersch, Georg; Winiwarter, Wilfried; Amon, Barbara

    2015-04-01

    Within the project FarmClim ("Farming for a better climate") we assessed recent N2O emissions from two selected regions in Austria. Our aim was to deepen the understanding of Austrian N2O fluxes regarding region specific properties. Currently, N2O emissions are estimated with the IPCC default emission factor which only considers the amount of N-input as an influencing factor for N2O emissions. We evaluated the IPCC default emission factor for its validity under spatially distinct environmental conditions. For this two regions for modeling with LandscapeDNDC have been identified in this project. The benefit of using LandscapeDNDC is the detailed illustration of microbial processes in the soil. Required input data to run the model included daily climate data, vegetation properties, soil characteristics and land management. The analysis of present agricultural practices was basis for assessing the hot spots and hot moments of nitrogen emissions on a regional scale. During our work with LandscapeDNDC we were able to adapt specific model algorithms to Austrian agricultural conditions. The model revealed a strong dependency of N2O emissions on soil type. We could estimate how strongly soil texture affects N2O emissions. Based on detailed soil maps with high spatial resolution we calculated region specific contribution to N2O emissions. Accordingly we differentiated regions with deviating gas fluxes compared to the predictions by the IPCC inventory methodology. Taking region specific management practices into account (tillage, irrigation, residuals) calculation of crop rotation (fallow, catch crop, winter wheat, barley, winter barley, sugar beet, corn, potato, onion and rapeseed) resulted in N2O emissions differing by a factor of 30 depending on preceding crop and climate. A maximum of 2% of N fertilizer input was emitted as N2O. Residual N in the soil was a major factor stimulating N2O emissions. Interannual variability was affected by varying N-deposition even in case

  19. Acidification Enhances Hybrid N2O Production Associated with Aquatic Ammonia-Oxidizing Microorganisms

    PubMed Central

    Frame, Caitlin H.; Lau, Evan; Nolan, E. Joseph; Goepfert, Tyler J.; Lehmann, Moritz F.

    2017-01-01

    Ammonia-oxidizing microorganisms are an important source of the greenhouse gas nitrous oxide (N2O) in aquatic environments. Identifying the impact of pH on N2O production by ammonia oxidizers is key to understanding how aquatic greenhouse gas fluxes will respond to naturally occurring pH changes, as well as acidification driven by anthropogenic CO2. We assessed N2O production rates and formation mechanisms by communities of ammonia-oxidizing bacteria (AOB) and archaea (AOA) in a lake and a marine environment, using incubation-based nitrogen (N) stable isotope tracer methods with 15N-labeled ammonium (15NH4+) and nitrite (15NO2−), and also measurements of the natural abundance N and O isotopic composition of dissolved N2O. N2O production during incubations of water from the shallow hypolimnion of Lake Lugano (Switzerland) was significantly higher when the pH was reduced from 7.54 (untreated pH) to 7.20 (reduced pH), while ammonia oxidation rates were similar between treatments. In all incubations, added NH4+ was the source of most of the N incorporated into N2O, suggesting that the main N2O production pathway involved hydroxylamine (NH2OH) and/or NO2− produced by ammonia oxidation during the incubation period. A small but significant amount of N derived from exogenous/added 15NO2− was also incorporated into N2O, but only during the reduced-pH incubations. Mass spectra of this N2O revealed that NH4+ and 15NO2− each contributed N equally to N2O by a “hybrid-N2O” mechanism consistent with a reaction between NH2OH and NO2−, or compounds derived from these two molecules. Nitrifier denitrification was not an important source of N2O. Isotopomeric N2O analyses in Lake Lugano were consistent with incubation results, as 15N enrichment of the internal N vs. external N atoms produced site preferences (25.0–34.4‰) consistent with NH2OH-dependent hybrid-N2O production. Hybrid-N2O formation was also observed during incubations of seawater from coastal Namibia

  20. Simultaneous measurement of stratospheric O3, H2O, CH4, and N2O profiles from infrared limb thermal emissions

    NASA Technical Reports Server (NTRS)

    Abbas, M. M.; Glenn, M. J.; Kunde, V. G.; Brasunas, J.; Conrath, B. J.; Maguire, W. C.; Herman, J. R.

    1987-01-01

    Thermal emission measurements of the earth's stratospheric limb were made with a cryogenically cooled high-resolution Michelson interferometer on a balloon flight launched from Palestine, TX, on Nov. 6, 1984. Infrared spectra for complete limb sequences were obtained over portions of the 700-1940/cm range with an unapodized spectral resolution of 0.03/cm for tangent heights varying from 13 to 39 km. The observed data from 1125 to 1425/cm have been analyzed for simultaneous measurement of O3, H2O, CH4, and N2O profiles. The analysis employs line-by-line and layer-by-layer radiative-transfer calculations, including curvature and refraction effects. The optimum use of geometric and spectral effects is made to obtain sharply peaked weighting functions. Contributions from stratospheric aerosol are included by measuring the light extinction within the window regions of the observed spectra. The retrieved constituent profiles are compared with measurements made with a variety of techniques by other groups. The comparison shows good agreement with the published data for all gases, indicating the capability of retrieving trace gas profiles from high-resolution thermal emission limb measurements.

  1. Troposphere-to-Stratosphere Transport in the Lowermost Stratosphere from Measurements of H2O, CO2, N2O and O3

    NASA Technical Reports Server (NTRS)

    Hintsa, E. J.; Boering, K. A.; Weinstock, E. M.; Anderson, J. G.; Gary, B. L.; Pfister, L.; Daube, B. C.; Wofsy, S. C.; Loewenstein, M.; Podolske, J.R.; hide

    1998-01-01

    The origin of air in the lowermost stratosphere is investigated with measurements from the NASA ER-2 aircraft. Air with high water vapor mixing ratios was observed in the stratosphere at theta-330-380 K near 40 N in May 1995, indicating the influence of intrusions of tropospheric air. Assuming that observed tracer-tracer relationships reflect mixing lines between tropospheric and stratospheric air masses, we calculate mixing ratios of H2O (12-24 ppmv) and CO2 for the admixed tropospheric air at theta=352-364 K. Temperatures on the 355 K surface at 20-40 N were low enough to dehydrate air to these values. While most ER-2 CO2 data in both hemispheres are consistent with tropical or subtropical air entering the lowermost stratosphere, measurements from May 1995 for theta<362 K suggest that entry of air from the midlatitude upper troposphere can occur in conjunction with mixing processes near the tropopause.

  2. Troposphere-to-Stratosphere Transport in the Lowermost Stratosphere from Measurements of H2O, CO2, N2O and O3

    NASA Technical Reports Server (NTRS)

    Hintsa, E. J.; Boering, K. A.; Weinstock, E. M.; Anderson, J. G.; Gary, B. L.; Pfister, L.; Daube, B. C.; Wofsy, S. C.; Loewenstein, M.; Podolske, J. R.

    1998-01-01

    The origin of air in the lowermost stratosphere is investigated with measurements from the NASA ER-2 aircraft. Air with high water vapor mixing ratios was observed in the stratosphere at theta = 330-380 K near 40 N in May 1995, indicating the influence of intrusions of tropospheric air. Assuming that observed tracer-tracer relationships reflect mixing lines between tropospheric and stratospheric air masses, we calculate mixing ratios of H2O (12-24 ppmv) and CO2 for the admixed tropospheric air at theta = 352-364 K. Temperatures on the 355 K surface at 20-40 N were low enough to dehydrate air to these values. While most ER-2 CO2 data in both hemispheres are consistent with tropical or subtropical air entering the lowermost stratosphere, measurements from May 1995 for theta < 362 K suggest that entry of air from the midlatitude upper troposphere can occur in conjunction with mixing processes near the tropopause.

  3. Troposphere-to-Stratosphere Transport in the Lowermost Stratosphere from Measurements of H2O, CO2, N2O, and O3

    NASA Technical Reports Server (NTRS)

    Hintsa, E. J.; Boering, K. A.; Weinstock, E. M.; Anderson, J. G.; Gary, B. L.; Pfister, L.; Daube, B. C.; Wofsy, S. C.; Loewenstein, M.; Podolske, J. R.; hide

    1998-01-01

    The origin of air in the lowermost stratosphere is investigated with measurements from the NASA ER-2 aircraft. Air with high water vapor mixing ratios was observed in the stratosphere at theta approximately 330-380 K near 40 N in May 1995, indicating the influence of intrusions of tropospheric air. Assuming that observed tracer-tracer relationships reflect mixing lines between tropospheric and stratospheric air masses, we calculate mixing ratios of H2O (12-24 ppmv) and CO2 for the admixed tropospheric air at theta = 352-364 K. Temperatures on the 355 K surface 20-40 N were low enough to dehydrate air to these values. While most ER-2 CO2 data in both hemispheres are consistent with tropical or subtropical air entering the lowermost stratosphere, measurements from May 1995 for theta < 362 K suggest that entry of air from the midlatitude upper troposphere can occur in conjunction with mixing processes near the tropopause.

  4. Troposphere-to-Stratosphere Transport in the Lowermost Stratosphere from Measurements of H2O, CO2, N2O and O3

    NASA Technical Reports Server (NTRS)

    Hintsa, E. J.; Boering, K. A.; Weinstock, E. M.; Anderson, J. G.; Gary, B. L.; Pfister, L.; Daube, B. C.; Wofsy, S. C.; Loewenstein, M.; Podolske, J. R.; hide

    1998-01-01

    The origin of air in the lowermost stratosphere is investigated with measurements from the NASA ER-2 aircraft. Air with high water vapor mixing ratios was observed in the stratosphere at theta about 330-380 K near 40N in May 1995, indicating the influence of intrusions of tropospheric air. Assuming that observed tracer-tracer relationships reflect mixing lines between tropospheric and stratospheric air masses, we calculate mixing ratios of H2O (12-24 ppmv) and CO2 for the admixed tropospheric air at theta =352-364 K. Temperatures on the 355 K surface at 20-40 N were low enough to dehydrate air to these values. while most ER-2 CO2 data in both hemispheres are consistent with tropical or subtropical air entering the lowermost stratosphere, measurements from May 1995 for theta <362 K suggest that entry of air from the midlatitude upper troposphere can occur in conjunction with mixing processes near the tropopause.

  5. Measurements of CH4, N2O, CO, H2O and O3 in the middle atmosphere by the ATMOS experiment on Spacelab 3

    NASA Technical Reports Server (NTRS)

    Gunson, M. R.; Farmer, C. B.; Norton, R. H.; Zander, R.; Rinsland, C. P.; Shaw, J. H.; Gao, Bo-Cai

    1989-01-01

    The volume mixing ratios of five minor gases (CH4, N2O, CO, H2O, and O3) were retrieved through the middle atmosphere from the analysis of 0.01/cm resolution infrared solar occultation spectra recorded near 28 N and 48 S latitudes with the ATMOS (Atmospheric Trace Molecule Spectroscopy) instrument, flown on board Spacelab 3. The results, which constitute the first simultaneous observations of continuous profiles through the middle atmosphere for these gases, are in general agreement with reported measurements from ground, balloon and satellite-based instruments for the same seasons. In detail, the vertical profiles of these gases show the effects of the upper and middle atmospheric transport patterns dominant during the season of these observations. The profiles inferred at different longitudes around 28 N suggest a near-uniform zonal distribution of these gases. Although based on fewer observations, the sunrise occultation measurements point to a larger variability in the vertical distribution of these gases at 48 S.

  6. Measurements and Modeling of Nitric Oxide Formation in Counterflow, Premixed CH4/O2/N2 Flames

    NASA Technical Reports Server (NTRS)

    Thomsen, D. Douglas; Laurendeau, Normand M.

    2000-01-01

    Laser-induced fluorescence (LIF) measurements of NO concentration in a variety of CH4/O2/N2 flames are used to evaluate the chemical kinetics of NO formation. The analysis begins with previous measurements in flat, laminar, premixed CH4/O2/N2 flames stabilized on a water-cooled McKenna burner at pressures ranging from 1 to 14.6 atm, equivalence ratios from 0.5 to 1.6, and volumetric nitrogen/oxygen dilution ratios of 2.2, 3.1 and 3.76. These measured results are compared to predictions to determine the capabilities and limitations of the comprehensive kinetic mechanism developed by the Gas Research Institute (GRI), version 2.11. The model is shown to predict well the qualitative trends of NO formation in lean-premixed flames, while quantitatively underpredicting NO concentration by 30-50%. For rich flames, the model is unable to even qualitatively match the experimental results. These flames were found to be limited by low temperatures and an inability to separate the flame from the burner surface. In response to these limitations, a counterflow burner was designed for use in opposed premixed flame studies. A new LIF calibration technique was developed and applied to obtain quantitative measurements of NO concentration in laminar, counterflow premixed, CH4/O2/N2 flames at pressures ranging from 1 to 5.1 atm, equivalence ratios of 0.6 to 1.5, and an N2/O2 dilution ratio of 3.76. The counterflow premixed flame measurements are combined with measurements in burner-stabilized premixed flames and counterflow diffusion flames to build a comprehensive database for analysis of the GRI kinetic mechanism. Pathways, quantitative reaction path and sensitivity analyses are applied to the GRI mechanism for these flame conditions. The prompt NO mechanism is found to severely underpredict the amount of NO formed in rich premixed and nitrogen-diluted diffusion flames. This underprediction is traced to uncertainties in the CH kinetics as well as in the nitrogen oxidation chemistry

  7. Climate change reduces the net sink of CH4 and N2O in a semiarid grassland.

    PubMed

    Dijkstra, Feike A; Morgan, Jack A; Follett, Ronald F; Lecain, Daniel R

    2013-06-01

    Atmospheric concentrations of methane (CH4 ) and nitrous oxide (N2 O) have increased over the last 150 years because of human activity. Soils are important sources and sinks of both potent greenhouse gases where their production and consumption are largely regulated by biological processes. Climate change could alter these processes thereby affecting both rate and direction of their exchange with the atmosphere. We examined how a rise in atmospheric CO2 and temperature affected CH4 and N2 O fluxes in a well-drained upland soil (volumetric water content ranging between 6% and 23%) in a semiarid grassland during five growing seasons. We hypothesized that responses of CH4 and N2 O fluxes to elevated CO2 and warming would be driven primarily by treatment effects on soil moisture. Previously we showed that elevated CO2 increased and warming decreased soil moisture in this grassland. We therefore expected that elevated CO2 and warming would have opposing effects on CH4 and N2 O fluxes. Methane was taken up throughout the growing season in all 5 years. A bell-shaped relationship was observed with soil moisture with highest CH4 uptake at intermediate soil moisture. Both N2 O emission and uptake occurred at our site with some years showing cumulative N2 O emission and other years showing cumulative N2 O uptake. Nitrous oxide exchange switched from net uptake to net emission with increasing soil moisture. In contrast to our hypothesis, both elevated CO2 and warming reduced the sink of CH4 and N2 O expressed in CO2 equivalents (across 5 years by 7% and 11% for elevated CO2 and warming respectively) suggesting that soil moisture changes were not solely responsible for this reduction. We conclude that in a future climate this semiarid grassland may become a smaller sink for atmospheric CH4 and N2 O expressed in CO2 -equivalents. © 2013 Blackwell Publishing Ltd.

  8. Microbial Nitrogen Cycle Hotspots in the Plant-Bed/Ditch System of a Constructed Wetland with N2O Mitigation.

    PubMed

    Wang, Shanyun; Wang, Weidong; Liu, Lu; Zhuang, Linjie; Zhao, Siyan; Su, Yu; Li, Yixiao; Wang, Mengzi; Wang, Cheng; Xu, Liya; Zhu, Guibing

    2018-05-24

    Artificial microbial nitrogen (N) cycle hotspots in the plant-bed/ditch system were developed and investigated based on intact core and slurry assays measurement using isotopic tracing technology, quantitative PCR and high-throughput sequencing. By increasing hydraulic retention time and periodically fluctuating water level in heterogeneous riparian zones, hotspots of anammox, nitrification, denitrification, ammonium (NH 4 + ) oxidation, nitrite (NO 2 - ) oxidation, nitrate (NO 3 - ) reduction and DNRA were all stimulated at the interface sediments, with the abundance and activity being about 1-3 orders of magnitude higher than those in nonhotspots. Isotopic pairing experiments revealed that in microbial hotspots, nitrite sources were higher than the sinks, and both NH 4 + oxidation (55.8%) and NO 3 - reduction (44.2%) provided nitrite for anammox, which accounted for 43.0% of N-loss and 44.4% of NH 4 + removal in riparian zones but did not involve nitrous oxide (N 2 O) emission risks. High-throughput analysis identified that bacterial quorum sensing mediated this anammox hotspot with B.fulgida dominating the anammox community, but it was B. anammoxidans and Jettenia sp. that contributed more to anammox activity. In the nonhotspot zones, the NO 2 - source (NO 3 - reduction dominated) was lower than the sink, limiting the effects on anammox. The in situ N 2 O flux measurement showed that the microbial hotspot had a 27.1% reduced N 2 O emission flux compared with the nonhotspot zones.

  9. [Emission of CH4, N2O and NH3 from vegetable field applied with animal manure composts].

    PubMed

    Wan, He-Feng; Zhao, Chen-Yang; Zhong, Jia; Ge, Zhen; Wei, Yuan-Song; Zheng, Jia-Xi; Wu, Yu-Long; Han, Sheng-Hui; Zheng, Bo-Fu; Li, Hong-Mei

    2014-03-01

    Greenhouse gas (GHG) emission from vegetable land is of great concern recently because agriculture land is one of the major sources contributing to global GHG emission. In this study, an experiment of Lactuca sativa L. land applied with different animal manure composts was carried out in a greenhouse vegetable land located in the surburb of Beijing to monitor the emission of GHG (CH4 and N2O) and ammonia in situ, and to analyze the affecting factors of GHG and ammonia emission. Results showed that the emission factors (EFs) of CH4 from Treatment NRM, RM and CF were 0.2%, 0.027% and 0.004%, respectively,the EFs of N2O from these three treatments were 0.18%, 0.63% and 0.74%, respectively, and the EFs of ammonia were 2.00%, 3.98% and 2.53%, respectively. CH4 emission flux was significantly affected by soil temperature and humidity, while N2O emission flux was related to soil temperature, surface temperature and humidity. The emission fluxes of CH4, N2O and NH3 were significantly affected by soil moisture, but there was little relation between CH4, N2O and NH3 emissions and the ambient temperature in the greenhouse.

  10. Infrared spectra of N2O-(ortho-D2)N and N2O-(HD)N clusters trapped in bulk solid parahydrogen.

    PubMed

    Lorenz, Britney D; Anderson, David T

    2007-05-14

    High-resolution infrared spectra of the clusters N2O-(ortho-D2)N and N2O-(HD)N, N=1-4, isolated in bulk solid parahydrogen at liquid helium temperatures are studied in the 2225 cm-1 region of the nu3 antisymmetric stretch of N2O. The clusters form during vapor deposition of separate gas streams of a precooled hydrogen mixture (ortho-D2para-H2 or HDpara-H2) and N2O onto a BaF2 optical substrate held at approximately 2.5 K in a sample-in-vacuum liquid helium cryostat. The cluster spectra reveal the N2O nu3 vibrational frequency shifts to higher energy as a function of N, and the shifts are larger for ortho-D2 compared to HD. These vibrational shifts result from the reduced translational zero-point energy for N2O solvated by the heavier hydrogen isotopomers. These spectra allow the N=0 peak at 2221.634 cm-1, corresponding to the nu3 vibrational frequency of N2O isolated in pure solid parahydrogen, to be assigned. The intensity of the N=0 absorption feature displays a strong temperature dependence, suggesting that significant structural changes occur in the parahydrogen solvation environment of N2O in the 1.8-4.9 K temperature range studied.

  11. Vibrational spectroscopy of NO + (H2O)n: Evidence for the intracluster reaction NO + (H2O)n --> H3O + (H2O)n - 2 (HONO) at n => 4

    NASA Astrophysics Data System (ADS)

    Choi, Jong-Ho; Kuwata, Keith T.; Haas, Bernd-Michael; Cao, Yibin; Johnson, Matthew S.; Okumura, Mitchio

    1994-05-01

    Infrared spectra of mass-selected clusters NO+(H2O)n for n=1 to 5 were recorded from 2700 to 3800 cm-1 by vibrational predissociation spectroscopy. Vibrational frequencies and intensities were also calculated for n=1 and 2 at the second-order Møller-Plesset (MP2) level, to aid in the interpretation of the spectra, and at the singles and doubles coupled cluster (CCSD) level energies of n=1 isomers were computed at the MP2 geometries. The smaller clusters (n=1 to 3) were complexes of H2O ligands bound to a nitrosonium ion NO+ core. They possessed perturbed H2O stretch bands and dissociated by loss of H2O. The H2O antisymmetric stretch was absent in n=1 and gradually increased in intensity with n. In the n=4 clusters, we found evidence for the beginning of a second solvation shell as well as the onset of an intracluster reaction that formed HONO. These clusters exhibited additional weak, broad bands between 3200 and 3400 cm-1 and two new minor photodissociation channels, loss of HONO and loss of two H2O molecules. The reaction appeared to go to completion within the n=5 clusters. The primary dissociation channel was loss of HONO, and seven vibrational bands were observed. From an analysis of the spectrum, we concluded that the n=5 cluster rearranged to form H3O+(H2O)3(HONO), i.e., an adduct of the reaction products.

  12. Interfacial RhO{sub x}/CeO{sub 2} sites as locations for low temperature N{sub 2}O dissociation

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    Cunningham, J.; Hickey, J.N.; Soria, J.

    Temperatures required for extensive N{sub 2}O dissociation to N{sub 2}, or to N{sub 2} plus O{sub 2}, over 0.5% RhO{sub x}/CeO{sub 2} materials, and over polycrystalline Rh{sub 2}O{sub 3} or CeO{sub 2}, are compared for preoxidised and for prereduced samples on the basis of conversions achieved in pulsed-reactant, continuous-flow and recirculatory microcatalytic reactors. Influences of sample prereduction or preoxidation upon those measurements and upon results from parallel ESR and FTIR studies of N{sub 2}O interactions with such materials are presented and compared. Over partially reduced 0.5% RhO{sub x}/CeO{sub 2} materials complete dissociation of N{sub 2}O pulses to N{sub 2} plusmore » O{sub 2} is obtained at temperatures 50-100{degrees} lower than those required for extensive dissociation over prereduced Rh{sub 2}O{sub 3}. Furthermore, N{sub 2} was the sole product from the latter. Higher ongoing N{sub 2}O conversions to N{sub 2} plus O{sub 2} at 623 K over 0.5% Rh/CeO{sub 2} in pulsed-reactant than in continuous-flow mode point to regeneration of active sites under helium flushing between pulses. The TPD profile for dioxygen release from Rhodia containing samples at temperatures 350-550 K is presented. ESR measurements reveal complementary effects of outgassings at temperatures, T{sub v}, {ge} 573 K upon the availability at RhO{sub x}/CeO{sub 2} surfaces of electron-excess sites reactive towards N{sub 2}O. Differences from observations over Rh{sub 2}O{sub 3} and CeO{sub 2} can be understood by attributing the low-temperature activity of RhO{sub x}/CeO{sub 2} to electron excess sites at microinterfaces between the dispersed Rhodia component and the Ceria support.« less

  13. Using Extractive FTIR to Measure N2O from Medium Heavy ...

    EPA Pesticide Factsheets

    This pilot project was designed to confirm that an FTIR could generate useful real-time data for non-regulated tailpipe emissions of concern to the EPA. This ability to generate useful modal data could be demonstrated if the mode shapes of regulated emissions measured by reference methods corroborated the mode shapes generated by the FTIR. For this purpose comparisons were to be made to CO2 and NOx. The purpose of this study was to determine whether the FTIR could be useful in better understanding the conditions under which N2O was emitted from the tailpipe. The study was designed to see whether there was correlation of the CO2 and NOx emissions as measured by CEMs and measured by the FTIR as well as the mode shapes of the real time data

  14. Emissions of N2O, CH4 and CO2 from tropical forest soils

    NASA Technical Reports Server (NTRS)

    Keller, Michael; Kaplan, Warren A.; Wofsy, Steven C.

    1986-01-01

    Emissions of nitrous oxide, methane, and carbon dioxide were measured at diverse locations in tropical forests of Brazil, Ecuador, and Puerto Rico using a static open chamber technique. Mean fluxes to the atmosphere were 1.7 x 10 to the 10th, -0.7 x 10 to the 10th, and 1.5 x 10 to the 14th molecules/sq cm per s for N2O, CH4, and CO2, respectively. The data indicate that tropical forests contribute a significant fraction of the global source for atmospheric N2O, about 40 percent of the current source, and possibly 75 percent of the preindustrial source. Methane is consumed by soils on average, but the sink is an insignificant part (less than 5 percent) of the atmospheric cycle for the gas. Emissions of CO2 from forest soils are higher at equatorial sites than at middle or high latitudes, as expected from ecological considerations. Soils emit CO2 at rates more than twice as large as the rate of carbon infall in litter; hence much of the emitted CO2 must arise from root metabolism.

  15. Quantitative comparison of in situ soil CO2 flux measurement methods

    Treesearch

    Jennifer D. Knoepp; James M. Vose

    2002-01-01

    Development of reliable regional or global carbon budgets requires accurate measurement of soil CO2 flux. We conducted laboratory and field studies to determine the accuracy and comparability of methods commonly used to measure in situ soil CO2 fluxes. Methods compared included CO2...

  16. Microcosm N2O emissions wth calibration

    EPA Pesticide Factsheets

    The dataset consists of measurements of soil nitrous oxide emissions from soils under three different amendments: glucose, cellulose, and manure. Data includes the four isotopomers of nitrous oxide (14N15N16O, 15N14N16O, 14N14N18O, 14N14N16O), and the site preference.This dataset is associated with the following publication:Chen , H., D. Williams , P. Deshmukh , F. Birgand, B. Maxwell, and J. Walker. Probing the Biological Sources of Soil N2O Emissions by Quantum Cascade Laser-Based 15N Isotopocule Analysis. SOIL SCIENCE SOCIETY OF AMERICA JOURNAL. Soil Science Society of America, Madison, WI, USA, 100(0): 175-181, (2016).

  17. Studies of CW lasing action in CO2-CO, N2O-CO, CO2-H2O, and N2O-H2O mixtures pumped by blackbody radiation

    NASA Technical Reports Server (NTRS)

    Abel, Robert W.; Christiansen, Walter H.; Li, Jian-Guo

    1988-01-01

    A proof of principle experiment to evaluate the efficacy of CO and H2O in increasing the power output for N2O and CO2 lasing mixtures has been conducted and theoretically analyzed for a blackbody radiation-pumped laser. The results for N2O-CO, CO2-CO, N2O-H2O and CO2-H2O mixtures are presented. Additions of CO to the N2O lasant increased power up to 28 percent for N2O laser mixtures, whereas additions of CO to the CO2 lasant, and the addition of H2O to both the CO2 and N2O lasants, resulted in decreased output power.

  18. Benthic fluxes in San Francisco Bay

    USGS Publications Warehouse

    Hammond, Douglas E.; Fuller, C.; Harmon, D.; Hartman, Blayne; Korosec, M.; Miller, L.G.; Rea, R.; Warren, S.; Berelson, W.; Hager, S.W.

    1985-01-01

    Measurements of benthic fluxes have been made on four occasions between February 1980 and February 1981 at a channel station and a shoal station in South San Francisco Bay, using in situ flux chambers. On each occasion replicate measurements of easily measured substances such as radon, oxygen, ammonia, and silica showed a variability (??1??) of 30% or more over distances of a few meters to tens of meters, presumably due to spatial heterogeneity in the benthic community. Fluxes of radon were greater at the shoal station than at the channel station because of greater macrofaunal irrigation at the former, but showed little seasonal variability at either station. At both stations fluxes of oxygen, carbon dioxide, ammonia, and silica were largest following the spring bloom. Fluxes measured during different seasons ranged over factors of 2-3, 3, 4-5, and 3-10 (respectively), due to variations in phytoplankton productivity and temperature. Fluxes of oxygen and carbon dioxide were greater at the shoal station than at the channel station because the net phytoplankton productivity is greater there and the organic matter produced must be rapidly incorporated in the sediment column. Fluxes of silica were greater at the shoal station, probably because of the greater irrigation rates there. N + N (nitrate + nitrite) fluxes were variable in magnitude and in sign. Phosphate fluxes were too small to measure accurately. Alkalinity fluxes were similar at the two stations and are attributed primarily to carbonate dissolution at the shoal station and to sulfate reduction at the channel station. The estimated average fluxes into South Bay, based on results from these two stations over the course of a year, are (in mmol m-2 d-1): O2 = -27 ?? 6; TCO2 = 23 ?? 6; Alkalinity = 9 ?? 2; N + N = -0.3 ?? 0.5; NH3 = 1.4 ?? 0.2; PO4 = 0.1 ?? 0.4; Si = 5.6 ?? 1.1. These fluxes are comparable in magnitude to those in other temperate estuaries with similar productivity, although the seasonal

  19. CO 2 uptake is offset by CH 4 and N 2O emissions in a poplar short-rotation coppice

    DOE PAGES

    Zenone, Terenzio; Zona, Donatella; Gelfand, Ilya; ...

    2015-04-18

    The need for renewable energy sources will lead to a considerable expansion in the planting of dedicated fast-growing biomass crops across Europe. These are commonly cultivated as short-rotation coppice (SRC), and currently poplar ( Populus spp.) is the most widely planted. In this study, we report the greenhouse gas (GHG) fluxes of carbon dioxide (CO 2), methane (CH 4) and nitrous oxide (N 2O) measured using eddy covariance technique in an SRC plantation for bioenergy production. Measurements were made during the period 2010–2013, that is, during the first two rotations of the SRC. The overall GHG balance of the 4more » years of the study was an emission of 1.90 (±1.37) Mg CO 2eq ha -1; this indicated that soil trace gas emissions offset the CO 2 uptake by the plantation. CH 4 and N 2O contributed almost equally to offset the CO 2 uptake of -5.28 (±0.67) Mg CO2eq ha -1 with an overall emission of 3.56 (±0.35) Mg CO 2eq ha -1 of N 2O and of 3.53 (±0.85) Mg CO 2eq ha-1 of CH 4. N 2O emissions mostly occurred during one single peak a few months after the site was converted to SRC; this peak comprised 44% of the total N 2O loss during the two rotations. Accurately capturing emission events proved to be critical for deriving correct estimates of the GHG balance. The nitrogen (N) content of the soil and the water table depth were the two drivers that best explained the variability in N 2O and CH 4, respectively. Here, this study underlines the importance of the ‘non-CO 2 GHGs’ on the overall balance. Further long-term investigations of soil trace gas emissions should monitor the N content and the mineralization rate of the soil, as well as the microbial community, as drivers of the trace gas emissions.« less

  20. The equilibrium constant for N2O5 = NO2 + NO3 - Absolute determination by direct measurement from 243 to 397 K

    NASA Technical Reports Server (NTRS)

    Cantrell, C. A.; Davidson, J. A.; Mcdaniel, A. H.; Shetter, R. E.; Calvert, J. G.

    1988-01-01

    Direct determinations of the equilibrium constant for the reaction N2O5 = NO2 + NO3 were carried out by measuring NO2, NO3, and N2O5 using long-path visible and infrared absorption spectroscopy as a function of temperature from 243 to 397 K. The first-order decay rate constant of N2O5 was experimentally measured as a function of temperature. These results are in turn used to derive a value for the rate coefficient for the NO-forming channel in the reaction of NO3 with NO2. The implications of the results for atmospheric chemistry, the thermodynamics of NO3, and for laboratory kinetics studies are discussed.

  1. A Theoretical Study of Vapour Phase Nucleation of the Rocket Propellant N2O4

    NASA Astrophysics Data System (ADS)

    Pal, P.

    2003-05-01

    The residual vapour of a rocket fuel at the venting stage develops a potential aerodynamic problem which is linked with the vapour phase nucleation phenomena of the propellant. This study, based entirely on molecular treatment, addresses the problem by focusing specifically on the N2O4 propellant which is used in the ARIANE flight. The phenomenon is examined by considering the thermodynamic free energies of N2O4 clusters, leading to the evaluation of nucleation flux rates of critical nuclei at incipient nucleation. Preliminary examinations of the kinetics of flux pulses provide basic explanation from a molecular perspective.

  2. Microbial Abundances Predict Methane and Nitrous Oxide Fluxes from a Windrow Composting System

    PubMed Central

    Li, Shuqing; Song, Lina; Gao, Xiang; Jin, Yaguo; Liu, Shuwei; Shen, Qirong; Zou, Jianwen

    2017-01-01

    Manure composting is a significant source of atmospheric methane (CH4) and nitrous oxide (N2O) that are two potent greenhouse gases. The CH4 and N2O fluxes are mediated by methanogens and methanotrophs, nitrifying and denitrifying bacteria in composting manure, respectively, while these specific bacterial functional groups may interplay in CH4 and N2O emissions during manure composting. To test the hypothesis that bacterial functional gene abundances regulate greenhouse gas fluxes in windrow composting systems, CH4 and N2O fluxes were simultaneously measured using the chamber method, and molecular techniques were used to quantify the abundances of CH4-related functional genes (mcrA and pmoA genes) and N2O-related functional genes (amoA, narG, nirK, nirS, norB, and nosZ genes). The results indicate that changes in interacting physicochemical parameters in the pile shaped the dynamics of bacterial functional gene abundances. The CH4 and N2O fluxes were correlated with abundances of specific compositional genes in bacterial community. The stepwise regression statistics selected pile temperature, mcrA and NH4+ together as the best predictors for CH4 fluxes, and the model integrating nirK, nosZ with pmoA gene abundances can almost fully explain the dynamics of N2O fluxes over windrow composting. The simulated models were tested against measurements in paddy rice cropping systems, indicating that the models can also be applicable to predicting the response of CH4 and N2O fluxes to elevated atmospheric CO2 concentration and rising temperature. Microbial abundances could be included as indicators in the current carbon and nitrogen biogeochemical models. PMID:28373862

  3. Pasture age effects on N[sub 2]O, NO and CH[sub 4] emissions in the Atlantic Lowlands of Costa Rica

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    Keller, M.; Reiners, W.A.; Veldkamp, E.

    A study conducted in Brazil indicated that N[sub 2]O emissions increased following forest conversion to pasture. Our first study in Costa Rica indicated the reverse. To explore this contradiction, we measured N[sub 2]O, NO, and CH[sub 4] emissions in a chronosequence of 8 sites comprising forest and derive pastures of ayes 2 to 25 years, all on the same soil type in the Atlantic Lowlands of Costa Rica. We found large differences through the chronosequence in the fluxes of these three gases. Flux changes were related to changes in available nitrogen, organic matter, moisture content, and bulk density in themore » soil. N[sub 2]O emissions from the 2-year pasture were much greater than from the forest. Emissions declined with pasture age so that 25-year pasture had much smaller emissions than the forest. NO emissions from young pastures were similar to forest emissions, then declined sharply with pasture age. Forest soils consumed CH[sub 4]. Pasture soils mainly produced CH[sub 4]. Prediction of the effects of land use change on trace gas fluxes in the tropics will require an assessment of the history and soil condition of individual land units.« less

  4. Can conservation tillage reduce N2O emissions on cropland transitioning to organic vegetable production?

    PubMed

    Chen, Guihua; Kolb, Lauren; Cavigelli, Michel A; Weil, Ray R; Hooks, Cerruti R R

    2018-03-15

    Nitrous oxide (N 2 O) is an important greenhouse gas and a catalyst of stratospheric ozone decay. Agricultural soils are the source of 75% of anthropogenic N 2 O emissions globally. Recently, significant attention has been directed at examining effects of conservation tillage on carbon sequestration in agricultural systems. However, limited knowledge is available regarding how these practices impact N 2 O emissions, especially for organic vegetable production systems. In this context, a three-year study was conducted in a well-drained sandy loam field transitioning to organic vegetable production in the Mid-Atlantic coastal plain of USA to investigate impacts of conservation tillage [strip till (ST) and no-till (NT)] and conventional tillage (CT) [with black plastic mulch (CT-BP) and bare-ground (CT-BG)] on N 2 O emissions. Each year, a winter cover crop mixture (forage radish: Raphanus sativus var. longipinnatus, crimson clover: Trifolium incarnatum L., and rye: Secale cereale L.) was grown and flail-mowed in the spring. Nearly 80% of annual N 2 O-nitrogen (N) emissions occurred during the vegetable growing season for all treatments. Annual N 2 O-N emissions were greater in CT-BP than in ST and NT, and greater in CT-BG than in NT, but not different between CT-BG and CT-BP, ST and NT, or CT-BG and ST. Conventional tillage promoted N mineralization and plastic mulch increased soil temperature, which contributed to greater N 2 O-N fluxes. Though water filled porosity in NT was higher and correlated well with N 2 O-N fluxes, annual N 2 O-N emissions were lowest in NT suggesting a lack of substrates for nitrification and denitrification processes. Crop yield was lowest in NT in Year 1 and CT-BP in Year 3 but yield-scaled N 2 O-N emissions were consistently greatest in CT-BP and lowest in NT each year. Our results suggest that for coarse-textured soils in the coastal plain with winter cover crops, conservation tillage practices may reduce N 2 O emissions in organic

  5. N2O, NO, N2 and CO2 emissions from tropical savanna and grassland of northern Australia: an incubation experiment with intact soil cores

    NASA Astrophysics Data System (ADS)

    Werner, C.; Reiser, K.; Dannenmann, M.; Hutley, L. B.; Jacobeit, J.; Butterbach-Bahl, K.

    2014-11-01

    Strong seasonal variability of hygric and thermal soil conditions are a defining environmental feature in northern Australia. However, how such changes affect the soil-atmosphere exchange of nitrous oxide (N2O), nitric oxide (NO) and dinitrogen (N2) is still not well explored. By incubating intact soil cores from four sites (three savanna, one pasture) under controlled soil temperatures (ST) and soil moisture (SM) we investigated the release of the trace gas fluxes of N2O, NO and carbon dioxide (CO2). Furthermore, the release of N2 due to denitrification was measured using the helium gas flow soil core technique. Under dry pre-incubation conditions NO and N2O emissions were very low (<7.0 ± 5.0 μg NO-N m-2 h-1; <0.0 ± 1.4 μg N2O-N m-2 h-1) or in the case of N2O, even a net soil uptake was observed. Substantial NO (max: 306.5 μg N m-2 h-1) and relatively small N2O pulse emissions (max: 5.8 ± 5.0 μg N m-2 h-1) were recorded following soil wetting, but these pulses were short lived, lasting only up to 3 days. The total atmospheric loss of nitrogen was generally dominated by N2 emissions (82.4-99.3% of total N lost), although NO emissions contributed almost 43.2% to the total atmospheric nitrogen loss at 50% SM and 30 °C ST incubation settings (the contribution of N2 at these soil conditions was only 53.2%). N2O emissions were systematically higher for 3 of 12 sample locations, which indicates substantial spatial variability at site level, but on average soils acted as weak N2O sources or even sinks. By using a conservative upscale approach we estimate total annual emissions from savanna soils to average 0.12 kg N ha-1 yr-1 (N2O), 0.68 kg N ha-1 yr-1 (NO) and 6.65 kg N ha-1 yr-1 (N2). The analysis of long-term SM and ST records makes it clear that extreme soil saturation that can lead to high N2O and N2 emissions only occurs a few days per year and thus has little impact on the annual total. The potential contribution of nitrogen released due to pulse events

  6. Flux pinning mechanism in codoped-MgB2 with Al2O3 and SiC

    NASA Astrophysics Data System (ADS)

    Kiafiroozkoohi, Narjess Sadat; Ghorbani, Shaban Reza; Arabi, Hadi

    2018-05-01

    MgB2 superconductor samples, co-doped with 0.02 wt of Al2O3 and 0.02 wt SiC, have been examined by M-H loop measurements and calculation of the critical current density based on the Bean model. Normalized volume pinning force, f = F/Fmax, as a function of the reduced magnetic field, h = H/Hmax has been obtained at each temperature. Hughochi flux pinning model, which was included the normal point pinning, the normal surface pinning, and the pinning based on spatial variation in the Ginzburg-Landau parameter, was used to study the flux pinning mechanisms. It was found that the Δκ effect and the normal point pinning mechanisms play the main role in the flux pinning at the magnetic field lower than Hmax and the contribution of the Δκ mechanism increases with the increasing temperature, while the contribution of normal point pinning mechanism decreases. At magnetic field larger than Hmax, the only mechanism that acts as the flux pinning was the normal surface pinning mechanism.

  7. Characterization And Partitioning Of CH4 And CO2 Eddy Flux Data Measured at NGEE-Arctic Sites

    NASA Astrophysics Data System (ADS)

    Dengel, S.; Chafe, O.; Curtis, J. B.; Biraud, S.; Torn, M. S.; Wullschleger, S. D.

    2017-12-01

    The high latitudes are experiencing rapid warming with permafrost ecosystems being highly vulnerable to this change. Since the advancement in Eddy Covariance (EC) measurements, the number of high latitude sites measuring greenhouse gases and energy (CO2, CH4 and H2O) fluxes is steadily increasing, with new sites being established each year. Data from these sites are not only valuable for annual carbon budget calculations, but also vital to the modeling community for improving their predictions of emission rates and trends. CH4 flux measurements are not as straightforward as CO2 fluxes. They tend to be less predictable or as easily interpretable as CO2 fluxes. Understanding CH4 emission patterns are often challenging. Moreover, gas flux fluctuations are spatially and temporally diverse, and in many cases event-based. An improvement in understanding would also contribute to improvements in the fidelity of model predictions. These rely on having high quality data, and thus will entail developing new QA/QC and gap-filling methods for Arctic systems, in particularly for CH4. Contributing to these challenges is the limited number of ancillary measurements carried out at many sites and the lack of standardized data processing, QA/QC, and gap-filling procedures, in particular for CH4. CO2, CH4, and energy flux measurements are ongoing at, both NGEE-Arctic/AmeriFlux, US-NGB (Arctic coastal plain), and US-NGC (subarctic tussock tundra) sites. The sites, with underlying continuous permafrost, show a high degree of inter-annual and seasonal variability in CH4 fluxes. In order to interpret this variability, we apply a variety of models, such as footprint characterization, generalized additive models, as well as artificial neural networks, in an attempt to decipher these diverse fluxes, patterns and events.

  8. Collisional Removal of OH (X (sup 2)Pi, nu=7) by O2, N2, CO2, and N2O

    NASA Technical Reports Server (NTRS)

    Knutsen, Karen; Dyer, Mark J.; Copeland, Richard A.

    1996-01-01

    Collisional removal rate constants for the OH (X 2PI, nu = 7) radical are measured for the colliders O2, CO2, and N2O, and an upper limit is established for N2. OH(nu = 4) molecules, generated in a microwave discharge flow cell by the reaction of hydrogen atoms with ozone, are excited to v = 7 by the output of a pulsed infrared laser via direct vibrational overtone excitation. The temporal evolution of the P = 7 population is probed as a function of the collider gas partial pressure by a time-delayed pulsed ultraviolet laser. Fluorescence from the B 21 + state is detected in the visible spectral region.

  9. [Effect of short-time drought process on denitrifying bacteria abundance and N2O emission in paddy soil].

    PubMed

    Lu, Jing; Liu, Jin-Bo; Sheng, Rong; Liu, Yi; Chen, An-Lei; Wei, Wen-Xue

    2014-10-01

    In order to investigate the impact of drying process on greenhouse gas emissions and denitrifying microorganisms in paddy soil, wetting-drying process was simulated in laboratory conditions. N2O flux, redox potential (Eh) were monitored and narG- and nosZ-containing denitrifiers abundances were determined by real-time PCR. N2O emission was significantly increased only 4 h after drying process began, and it was more than 6 times of continuous flooding (CF) at 24 h. In addition, narG and nosZ gene abundances were increased rapidly with the drying process, and N2O emission flux was significantly correlated with narG gene abundance (P < 0.01). Our results indicated that the narG-containing deniteifiers were the main driving microorganisms which caused the N2O emission in the short-time drought process in paddy soil.

  10. Cross section data sets for electron collisions with H2, O2, CO, CO2, N2O and H2O

    NASA Astrophysics Data System (ADS)

    Anzai, K.; Kato, H.; Hoshino, M.; Tanaka, H.; Itikawa, Y.; Campbell, L.; Brunger, M. J.; Buckman, S. J.; Cho, H.; Blanco, F.; Garcia, G.; Limão-Vieira, P.; Ingólfsson, O.

    2012-02-01

    We review earlier cross section data sets for electron-collisions with H2, O2, CO, CO2, H2O and N2O, updated here by experimental results for their electronic states. Based on our recent measurements of differential cross sections for the electronic states of those molecules, integral cross sections (ICSs) are derived by applying a generalized oscillator strength analysis and then assessed against theory (BE f-scaling [Y.-K. Kim, J. Chem. Phys. 126, 064305 (2007)]). As they now represent benchmark electronic state cross sections, those ICSs for the above molecules are added into the original cross section sets taken from the data reviews for H2, O2, CO2 and H2O (the Itikawa group), and for CO and N2O (the Zecca group).

  11. Measured and simulated nitrogen fluxes after field application of food-processing and municipal organic wastes.

    PubMed

    Parnaudeau, V; Génermont, S; Hénault, C; Farrugia, A; Robert, P; Nicolardot, B

    2009-01-01

    The aims of this study were to (i) assess N fluxes (mineralization, volatilization, denitrification, leaching) caused by spreading various organic wastes from food-processing industries during a field experiment, and (ii) to identify the main factors affecting N transformation processes after field spreading. Experimental treatments including the spreading of six types of waste and a control soil were set up in August 2000 and studied for 22 mo under bare soil conditions. Ammonia and nitrous oxide emissions, and nitrogen mineralization were measured in experimental devices and extrapolated to field conditions or computed in calculation models. The ammonia emissions varied from 80 to 580 g kg(-1) NH4+-N applied, representing 0 to 90 g N kg(-1) total N applied. Under these meteorologically favorable conditions (dry and warm weather), waste pH was the main factor affecting volatilization rates. Cumulated N2O-N fluxes were estimated at 2 to 5 g kg(-1) total N applied, which was quite low due to the low soil water content during the experimental period; water-filled pore space (WFPS) was confirmed as the main factor affecting N2O fluxes. Nitrogen mineralization from wastes represented 126 to 723 g N kg(-1) organic N added from the incorporation date to 14 May 2001 and was not related to the organic C to organic N ratio of wastes. Nitrogen lost by leaching during the equivalent period ranged from 30 to 890 g kg(-1) total N applied. The highest values were obtained for wastes having the highest inorganic N content and mineralization rates.

  12. Fungi regulate response of N2O production to warming and grazing in a Tibetan grassland

    NASA Astrophysics Data System (ADS)

    Zhong, Lei; Wang, Shiping; Xu, Xingliang; Wang, Yanfen; Rui, Yichao; Zhou, Xiaoqi; Shen, Qinhua; Wang, Jinzhi; Jiang, Lili; Luo, Caiyun; Gu, Tianbao; Ma, Wenchao; Chen, Guanyi

    2018-03-01

    Lack of understanding of the effects of warming and winter grazing on soil fungal contribution to nitrous oxide (N2O) production has limited our ability to predict N2O fluxes under changes in climate and land use management, because soil fungi play an important role in driving terrestrial N cycling. Here, we examined the effects of 10 years' warming and winter grazing on soil N2O emissions potential in an alpine meadow. Our results showed that soil bacteria and fungi contributed 46 % and 54 % to nitrification, and 37 % and 63 % to denitrification, respectively. Neither warming nor winter grazing affected the activity of enzymes responsible for overall nitrification and denitrification. However, warming significantly increased the enzyme activity of bacterial nitrification and denitrification to 53 % and 55 %, respectively. Warming significantly decreased enzyme activity of fungal nitrification and denitrification to 47 % and 45 %, respectively, while winter grazing had no such effect. We conclude that soil fungi could be the main source for N2O production potential in the Tibetan alpine grasslands. Warming and winter grazing may not affect the potential for soil N2O production potential, but climate warming can alter biotic pathways responsible for N2O production. These findings indicate that characterizing how fungal nitrification/denitrification contributes to N2O production, as well as how it responds to environmental and land use changes, can advance our understanding of N cycling. Therefore, our results provide some new insights about ecological controls on N2O production and lead to refine greenhouse gas flux models.

  13. Eddy covariance fluxes of the NO-O3-NO2 triad above the forest canopy at the ATTO Site in the Amazon Basin

    NASA Astrophysics Data System (ADS)

    Tsokankunku, Anywhere; Wolff, Stefan; Sörgel, Matthias; Berger, Martina; Zelger, Michael; Dlugi, Ralf

    2017-04-01

    Nitrogen monoxide (NO) and nitrogen dioxide (NO2) (denoted together as NOx) determine the abundance of the tropospheric oxidants OH, O3 and NO3 that regulate atmospheric self-cleaning. The three reactive trace gases NO, NO2 and O3 undergo a series of interconnected photochemical reactions and are often referred to as the NO-O3-NO2 triad. Ozone deposition is mainly controlled by stomatal uptake, thus contributes to oxidative stress for the plants. Similarly, nitrogen dioxide from above or below the canopy is deposited to leaves through stomatal uptake. NO emissions from soils contribute to above canopy O3 formation and accelerate OH recycling. Therefore, quantification of the exchange fluxes of these species between the atmosphere and the biosphere are important for atmospheric chemistry and ecosystem research as well. The eddy covariance method is state of the art for direct measurements of ecosystem fluxes of trace gases. Eddy covariance measurements of NOx in pristine environments are rare because of lack of availability of instruments with the required precision to resolve concentrations characteristic of these environments. The Amazon Tall Tower Observatory (ATTO) is located in a pristine rainforest environment in the Amazon basin about 150 km northeast of the city of Manaus. It is the ideal site for studying the biosphere-atmosphere exchange of the NO-O3-NO2 triad, being largely undisturbed by anthropogenic sources. During an intensive measurement campaign in November 2015 at the ATTO site, measurements of NO, NO2 and O3 were carried out at 42 m above ground level on the 80 m walk-up tower with a fast (5 Hz) and sensitive (< 30 ppt) instrument (CLD790SR2, Eco Physics) for NO and NO2 and with 10 Hz for O3 (Enviscope). Additionally, measurements of turbulent and micrometeorological parameters were conducted with a profile of 3-dimensional sonic anemometers and meteorological sensors for temperature, humidity and radiation. Vertical concentration profile

  14. Diffuse CO2 fluxes from Santiago and Congro volcanic lakes (São Miguel, Azores archipelago)

    NASA Astrophysics Data System (ADS)

    Andrade, César; Cruz, José; Viveiros, Fátima; Branco, Rafael

    2017-04-01

    Diffuse CO2 degassing occurring in Santiago and Congro lakes, both located in depressions associated to maars from São Miguel Island (Azores, Portugal), was studied through detailed flux measurements. Four sampling campaigns were developed between 2013 and 2016 in each water body, split by the cold and wet seasons. São Miguel has an area of 744.6 km2, being the largest island of the archipelago. The geology of the island is dominated by three quiescent central volcanoes (Sete Cidades, Fogo and Furnas), linked by volcanic fissural zones (Picos and Congro Fissural Volcanic systems). The oldest volcanic systems of the island are located in its eastern part (Povoação-Nordeste). Santiago lake, with a surface area of 0.26 km2 and a depth of 30.5 m, is located inside a maar crater in the Sete Cidades volcano at an altitude of 355 m. The watershed of the lake has an area of 0.97 km2 and a surface flow estimated as 1.54x10 m3/a. A total of 1612 CO2 flux measurements using the accumulation chamber method were made at Santiago lake, 253 in the first campaign (November 2013), and 462, 475 and 422 in the three other campaigns, respectively, in April 2014, September 2016 and December 2016. The total CO2 flux estimated for this lake varies between 0.4 t d-1 and 0.59 t d-1, for the surveys performed, respectively, in November 2013 and September 2016; higher CO2 outputs of 1.57 and 5.87 t d-1 were calculated for the surveys carried out in April 2014 and December 2016. These higher CO2 emissions were associated with a period without water column stratification. Similarly to Santiago lake, Congro lake is located inside a maar, in the Congro Fissural Volcanic system, and has a surface area of 0.04 km2 with 18.5 m depth and a storage of about 2.4x105 m3/a. The lake, located at an altitude of 420 m, is fed by a watershed with an area of 0.33 km2 and a runoff estimated as about 8x104 m3/a. In Congro lake a total of 713 CO2 flux measurements were performed during four surveys from

  15. Hotspots of soil N 2O emission enhanced through water absorption by plant residue

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    Kravchenko, A. N.; Toosi, E. R.; Guber, A. K.

    N 2O is a highly potent greenhouse gas and arable soils represent its major anthropogenic source. Field-scale assessments and predictions of soil N 2O emission remain uncertain and imprecise due to the episodic and microscale nature of microbial N 2O production, most of which occurs within very small discrete soil volumes. Such hotspots of N 2O production are often associated with decomposing plant residue. Here we quantify physical and hydrological soil characteristics that lead to strikingly accelerated N 2O emissions in plant residue-induced hotspots. Results reveal a mechanism for microscale N 2O emissions: water absorption by plant residue that createsmore » unique micro-environmental conditions, markedly different from those of the bulk soil. Moisture levels within plant residue exceeded those of bulk soil by 4–10-fold and led to accelerated N 2O production via microbial denitrification. The presence of large (Ø >35 μm) pores was a prerequisite for maximized hotspot N 2O production and for subsequent diffusion to the atmosphere. Understanding and modelling hotspot microscale physical and hydrologic characteristics is a promising route to predict N 2O emissions and thus to develop effective mitigation strategies and estimate global fluxes in a changing environment.« less

  16. Hotspots of soil N2O emission enhanced through water absorption by plant residue

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    Kravchenko, A. N.; Toosi, E. R.; Guber, A. K.

    N2O is a highly potent greenhouse gas and arable soils represent its major anthropogenic source. Field-scale assessments and predictions of soil N2O emission remain uncertain and imprecise due to the episodic and microscale nature of microbial N2O production, most of which occurs within very small discrete soil volumes. Such hotspots of N2O production are often associated with decomposing plant residue. Here we quantify physical and hydrological soil characteristics that lead to strikingly accelerated N2O emissions in plant residue-induced hotspots. Results reveal a mechanism for microscale N2O emissions: water absorption by plant residue that creates unique micro-environmental conditions, markedly different frommore » those of the bulk soil. Moisture levels within plant residue exceeded those of bulk soil by 4–10-fold and led to accelerated N2O production via microbial denitrification. The presence of large (Ø >35 μm) pores was a prerequisite for maximized hotspot N2O production and for subsequent diffusion to the atmosphere. Understanding and modelling hotspot microscale physical and hydrologic characteristics is a promising route to predict N2O emissions and thus to develop effective mitigation strategies and estimate global fluxes in a changing environment.« less

  17. Hotspots of soil N 2O emission enhanced through water absorption by plant residue

    DOE PAGES

    Kravchenko, A. N.; Toosi, E. R.; Guber, A. K.; ...

    2017-06-05

    N 2O is a highly potent greenhouse gas and arable soils represent its major anthropogenic source. Field-scale assessments and predictions of soil N 2O emission remain uncertain and imprecise due to the episodic and microscale nature of microbial N 2O production, most of which occurs within very small discrete soil volumes. Such hotspots of N 2O production are often associated with decomposing plant residue. Here we quantify physical and hydrological soil characteristics that lead to strikingly accelerated N 2O emissions in plant residue-induced hotspots. Results reveal a mechanism for microscale N 2O emissions: water absorption by plant residue that createsmore » unique micro-environmental conditions, markedly different from those of the bulk soil. Moisture levels within plant residue exceeded those of bulk soil by 4–10-fold and led to accelerated N 2O production via microbial denitrification. The presence of large (Ø >35 μm) pores was a prerequisite for maximized hotspot N 2O production and for subsequent diffusion to the atmosphere. Understanding and modelling hotspot microscale physical and hydrologic characteristics is a promising route to predict N 2O emissions and thus to develop effective mitigation strategies and estimate global fluxes in a changing environment.« less

  18. Micrometeorological flux measurements of aerosol and gases above Beijing

    NASA Astrophysics Data System (ADS)

    Nemitz, Eiko; Langford, Ben; Mullinger, Neil; Cowan, Nicholas; Coyle, Mhairi; Acton, William Joe; Lee, James; Fu, Pingqing

    2017-04-01

    Air pollution is estimated to cause 1.6 million premature deaths in China every year and in the winter 2016/17 Beijing had to issue health alerts and put in place ad hoc limitations on industrial and vehicular activity. Much of this pollution is attributed to emissions from industrial processes and in particular coal combustion. By contrast, the diffuse pollutant sources within the city are less well understood. This includes, e.g., emissions from the Beijing traffic fleet, the sewage system, food preparation, solid fuel combustion in the streets and small industrial processes. Within the framework of a major UK-Chinese collaboration to study air pollution and its impact on human health in Beijing, we therefore measured fluxes of a large range of pollutants from a height of 102 m on the 325 m meteorological tower at the Institute of Atmospheric Physics. Several instruments were mounted at 102 m: fluxes of CO2 and H2O were measured with an infrared gas analyser (LiCOR 7500) and fluxes of ozone with a combination of a relative fast-response ozone analyser (ROFI) and a 2B absolute O3 instrument. Total particle number fluxes were measured with a condensation particle counter (TSI CPC 3785), and size-segregated fluxes over the size range 0.06 to 20 μm with a combination of an optical Ultrafine High Sensitivity Aerosol Spectrometer (UHSAS) and an Aerodynamic Particle Sizer Spectrometer (TSI APS3321). Ammonia (NH3) fluxes were measured for the first time above the urban environment using an Aerodyne compact quantum cascade laser (QCL). In addition, composition resolved aerosol fluxes were measured with an Aerodyne Aerosol Mass Spectrometer (HR-ToF-AMS), operated in a measurement container at the bottom of the tower, which subsampled from a 120 m long copper tube (15 mm OD). The analysis so far suggests that, due to often low wind speeds, fluxes were at times de-coupled from the surface. Fluxes normalised by CO2, a tracer for the amount of fossil fuel consumed, should be

  19. Annual Net Community Production in the Western Subtropical North Pacific Determined from Argo-O2 Measurements

    NASA Astrophysics Data System (ADS)

    Yang, B.; Emerson, S. R.; Bushinsky, S. M.

    2016-02-01

    Export of organic carbon from the surface ocean to depth (the biological pump) helps maintain the pCO2 of the atmosphere and the O2 content of the oxygen minimum zones of the ocean. In the upper ocean, at steady state over a seasonal cycle the net organic carbon export is equal to the Annual Net Community Production (ANCP). The geographic distribution of this quantity determined by satellite-predicted Net Primary Production (NPP) and the recycling efficiency in the euphotic zone is more heterogeneous than the limited experimental estimates of ANCP. We evaluate the relationship between these two estimates of ANCP in the subtropical Western North Pacific Ocean ( 165o E and 20o N) using oxygen measurements on Argo Floats. In January of 2015 we deployed four floats with Anderaa oxygen sensors attached to a 60 cm stick on top of the float end cap, which can be readily calibrated against atmospheric pO2. We present data from these floats and air-sea oxygen flux calculations. The degree of oxygen supersaturation in summer is 1-2 percent, and in winter it fluctuates between being over and undersaturated. Evaluating the role of bubbles in winter is critical to an accurate determination of the annual flux. While there is not a full year of data at the time of writing this abstract, there will be when the Ocean Science meeting is held. So far, after nine months of measurements, there is a net flux of oxygen to the atmosphere, indicating that photosynthesis exceeds respiration. In February we will present a full annual cycle of air-sea oxygen flux and an estimate of ANCP in this very rarely studied region of the ocean.

  20. Effects of Carbon and Cover Crop Residues on N2O and N2 Emissions

    NASA Astrophysics Data System (ADS)

    Burger, M.; Cooperman, Y.; Horwath, W. R.

    2016-12-01

    In Mediterranean climate, nitrous oxide emissions occurring with the first rainfall after the dry summer season can contribute up to 50% of agricultural systems' total annual emissions, but the drivers of these emissions have not been clearly identified, and there are only few measurements of atmospheric nitrogen (N2) production (denitrification) during these events. In lab incubations, we investigated N2O and N2 production, gross ammonification and nitrification, and microbial N immobilization with wet-up in soil from a vineyard that was previously fallow or where cover crop residue had been incorporated the previous spring. Before the first rainfall, we measured 120 mg dissolved organic carbon (DOC-C) kg-1 soil in the 0-5 cm layer of this vineyard, and after the rain 10 mg DOC-C kg-1, while nitrate levels before the rain were <5 mg N kg-1 in fallow and <10 mg N kg-1 in previously cover cropped soil. The N2O/N2 production was 2, 7, 9, and 86% in fallow, legume-grass mixture, rye, and legume cover cropped soil. The N2O/N2 ratio tended to increase with lower DOC (post-rain) levels in the soil. The results suggest that accumulated carbon in dry surface soil is the main driving factor of N2O and N2 emissions through denitrification with the first rainfall after prolonged dry periods.

  1. Effect of air composition (N2, O2, Ar, and H2O) on CO2 and CH4 measurement by wavelength-scanned cavity ring-down spectroscopy: calibration and measurement strategy

    NASA Astrophysics Data System (ADS)

    Nara, H.; Tanimoto, H.; Tohjima, Y.; Mukai, H.; Nojiri, Y.; Katsumata, K.; Rella, C. W.

    2012-11-01

    We examined potential interferences from water vapor and atmospheric background gases (N2, O2, and Ar), and biases by isotopologues of target species, on accurate measurement of atmospheric CO2 and CH4 by means of wavelength-scanned cavity ring-down spectroscopy (WS-CRDS). Changes of the background gas mole fractions in the sample air substantially impacted the CO2 and CH4 measurements: variation of CO2 and CH4 due to relative increase of each background gas increased as Ar < O2 < N2, suggesting similar relation for the pressure-broadening effects (PBEs) among the background gas. The pressure-broadening coefficients due to variations in O2 and Ar for CO2 and CH4 are empirically determined from these experimental results. Calculated PBEs using the pressure-broadening coefficients are linearly correlated with the differences between the mole fractions of O2 and Ar and their ambient abundances. Although the PBEs calculation showed that impact of natural variation of O2 is negligible on the CO2 and CH4 measurements, significant bias was inferred for the measurement of synthetic standard gases. For gas standards balanced with purified air, the PBEs were estimated to be marginal (up to 0.05 ppm for CO2 and 0.01 ppb for CH4) although the PBEs were substantial (up to 0.87 ppm for CO2 and 1.4 ppb for CH4) for standards balanced with synthetic air. For isotopic biases on CO2 measurements, we compared experimental results and theoretical calculations, which showed excellent agreement within their uncertainty. We derived instrument-specific water correction functions empirically for three WS-CRDS instruments (Picarro EnviroSense 3000i, G-1301, and G-2301), and evaluated the transferability of the water correction function from G-1301 among these instruments. Although the transferability was not proven, no significant difference was found in the water vapor correction function for the investigated WS-CRDS instruments as well as the instruments reported in the past studies

  2. Simulation of atmospheric N2O with GEOS-Chem and its adjoint: evaluation of observational constraints

    NASA Astrophysics Data System (ADS)

    Wells, K. C.; Millet, D. B.; Bousserez, N.; Henze, D. K.; Chaliyakunnel, S.; Griffis, T. J.; Luan, Y.; Dlugokencky, E. J.; Prinn, R. G.; O'Doherty, S.; Weiss, R. F.; Dutton, G. S.; Elkins, J. W.; Krummel, P. B.; Langenfelds, R.; Steele, L. P.; Kort, E. A.; Wofsy, S. C.; Umezawa, T.

    2015-07-01

    We describe a new 4D-Var inversion framework for N2O based on the GEOS-Chem chemical transport model and its adjoint, and apply this framework in a series of observing system simulation experiments to assess how well N2O sources and sinks can be constrained by the current global observing network. The employed measurement ensemble includes approximately weekly and quasi-continuous N2O measurements (hourly averages used) from several long-term monitoring networks, N2O measurements collected from discrete air samples aboard a commercial aircraft (CARIBIC), and quasi-continuous measurements from an airborne pole-to-pole sampling campaign (HIPPO). For a two-year inversion, we find that the surface and HIPPO observations can accurately resolve a uniform bias in emissions during the first year; CARIBIC data provide a somewhat weaker constraint. Variable emission errors are much more difficult to resolve given the long lifetime of N2O, and major parts of the world lack significant constraints on the seasonal cycle of fluxes. Current observations can largely correct a global bias in the stratospheric sink of N2O if emissions are known, but do not provide information on the temporal and spatial distribution of the sink. However, for the more realistic scenario where source and sink are both uncertain, we find that simultaneously optimizing both would require unrealistically small errors in model transport. Regardless, a bias in the magnitude of the N2O sink would not affect the a posteriori N2O emissions for the two-year timescale used here, given realistic initial conditions, due to the timescale required for stratosphere-troposphere exchange (STE). The same does not apply to model errors in the rate of STE itself, which we show exerts a larger influence on the tropospheric burden of N2O than does the chemical loss rate over short (< 3 year) timescales. We use a stochastic estimate of the inverse Hessian for the inversion to evaluate the spatial resolution of emission

  3. NO versus N2O emissions from an NH4 +-amended Bermuda grass pasture

    NASA Astrophysics Data System (ADS)

    Hutchinson, G. L.; Brams, E. A.

    1992-06-01

    We used an enclosure technique to monitor soil NO and N2O emissions during early summer regrowth of Bermuda grass (Cynodon dactylon) on sandy loam in a humid, subtropical region of southern Texas. The evolution of both gases was substantially higher from plots harvested at the beginning of the experiment and fertilized 5 days later with 52 kg N ha-1 as (NH4)2SO4 than from plots not harvested or fertilized. Emission of NO, but not N2O, was stimulated by clipping and removing the grass, probably because eliminating the shading provided by the dense grass canopy changed these plots from cooler to warmer than unharvested plots, thereby stimulating the activity of soil microorganisms responsible for NO production. Neither gas flux was significantly affected by application of N until the next rainfall dissolved and moved the surface-applied fertilizer into the soil. Immediately thereafter, emissions of NO and N2O increased dramatically to peaks of 160 and 12 g N ha-1 d-1, respectively, and then declined at rates that closely paralleled the nitrification rate of added NH4+, indicating that the gases resulted from the activity of nitrifying microorganisms, rather than denitrifiers. Nitric oxide emissions during the 9-week measurement period averaged 7.2 times greater than N2O emissions and accounted for 3.2% of the added N. The data indicate that humid, subtropical grasslands, which not only have large geographical extent but also have been subject to intense anthropogenic disturbance, contribute significantly to the global atmospheric NOx budget.

  4. NO versus N2O emissions from an NH4(+)-amended Bermuda grass pasture

    NASA Technical Reports Server (NTRS)

    Hutchinson, G. L.; Brams, E. A.

    1992-01-01

    An enclosure technique is used to monitor soil NO and N2O emissions during early summer regrowth of Bermuda grass (Cynodon dactylon) on sandy loam in a humid, subtropical region of southern Texas. The evolution of both gases was substantially higher from plots harvested at the beginning of the experiment and fertilized five days later with 52 kg N/ha as (NH4)2SO4 than from plots not harvested or fertilized. Emission of NO, but not N2O, was stimulated by clipping and removing the grass, probably because eliminating the shading provided by the dense grass canopy changed these plots from cooler to warmer than unharvested plots, thereby stimulating the activity of soil microorganisms responsible for NO production. Neither gas flux was significantly affected by application of N until the next rainfall dissolved and moved the surface-applied fertilizer into the soil. Immediately thereafter, emissions of NO and N2O increased dramatically to peaks of 160 and 12 g N/ha/d, respectively, and then declined at rates that closely parallel the nitrification rate of added NH4(+), indicating that the gases resulted from the activity of nitrifying microorganisms, rather than denitrifiers. Nitric oxide emissions during the nine-week measurement period averaged 7.2 times greater than N2O emissions and accounted for 3.2 percent of the added N. The data indicate that humid, subtropical grasslands, which not only have large geographical extent but also have been subject to intense anthropogenic disturbance, contribute significantly to the global atmospheric NO(x) budget.

  5. Biogenic CH4 and N2O emissions overwhelm land CO2 sink in Asia: Toward a full GHG budget

    NASA Astrophysics Data System (ADS)

    Tian, H.

    2017-12-01

    The recent global assessment indicates the terrestrial biosphere as a net source of greenhouse gases to the atmosphere (Tian et al Nature 2016). The fluxes of greenhouse gases (GHG) vary by region. Both TD and BU approaches indicate that human-caused biogenic fluxes of CO2, CH4 and N2O in the biosphere of Southern Asia led to a large net climate warming effect, because the 100-year cumulative effects of CH4 and N2O emissions together exceed that of the terrestrial CO2 sink. Southern Asia has about 90% of the global rice fields and represents more than 60% of the world's nitrogen fertilizer consumption, with 64%-81% of CH4 emissions and 36%-52% of N2O emissions derived from the agriculture and waste sectors. Given the large footprint of agriculture in Southern Asia, improved fertilizer use efficiency, rice management and animal diets could substantially reduce global agricultural N2O and CH4 emissions. This study highlights the importance of including all three major GHGs in regional climate impact assessments, mitigation option and climate policy development.

  6. Diagnosing ozone recovery using the O3-N2O relationship

    NASA Astrophysics Data System (ADS)

    Butler, A. H.; Gao, R. S.; Maycock, A.; Portmann, R. W.; Thornberry, T. D.; Rosenlof, K. H.; Fahey, D. W.

    2016-12-01

    The ubiquitous compact correlation between collocated values of stratospheric ozone (O3) and the tracer nitrous oxide (N2O) results from the stratospheric photochemical processes that produce ozone and destroy N2O combined with common transport and mixing processes. Changes in the correlation slope under certain circumstances reflect changes in the production and loss balance of ozone. This approach has been used extensively to diagnose and quantify ozone loss in polar spring. Using a coupled atmosphere-ocean model with interactive chemistry (CESM/WACCM), we show that this relationship can be used to diagnose ozone recovery in the lower extratropical stratosphere. We then consider in situ measurements of O3 and N2O from ATTREX, GloPac, and HIPPO as well as satellite measurements from ACE and Aura MLS to consider whether ozone recovery can be detected in observations during the period 2004-2016.

  7. Actinobacterial Nitrate Reducers and Proteobacterial Denitrifiers Are Abundant in N2O-Metabolizing Palsa Peat

    PubMed Central

    Palmer, Katharina

    2012-01-01

    Palsa peats are characterized by elevated, circular frost heaves (peat soil on top of a permanently frozen ice lens) and are strong to moderate sources or even temporary sinks for the greenhouse gas nitrous oxide (N2O). Palsa peats are predicted to react sensitively to global warming. The acidic palsa peat Skalluvaara (approximate pH 4.4) is located in the discontinuous permafrost zone in northwestern Finnish Lapland. In situ N2O fluxes were spatially variable, ranging from 0.01 to −0.02 μmol of N2O m−2 h−1. Fertilization with nitrate stimulated in situ N2O emissions and N2O production in anoxic microcosms without apparent delay. N2O was subsequently consumed in microcosms. Maximal reaction velocities (vmax) of nitrate-dependent denitrification approximated 3 and 1 nmol of N2O per h per gram (dry weight [gDW]) in soil from 0 to 20 cm and below 20 cm of depth, respectively. vmax values of nitrite-dependent denitrification were 2- to 5-fold higher than the vmax nitrate-dependent denitrification, and vmax of N2O consumption was 1- to 6-fold higher than that of nitrite-dependent denitrification, highlighting a high N2O consumption potential. Up to 12 species-level operational taxonomic units (OTUs) of narG, nirK and nirS, and nosZ were retrieved. Detected OTUs suggested the presence of diverse uncultured soil denitrifiers and dissimilatory nitrate reducers, hitherto undetected species, as well as Actino-, Alpha-, and Betaproteobacteria. Copy numbers of nirS always outnumbered those of nirK by 2 orders of magnitude. Copy numbers of nirS tended to be higher, while copy numbers of narG and nosZ tended to be lower in 0- to 20-cm soil than in soil below 20 cm. The collective data suggest that (i) the source and sink functions of palsa peat soils for N2O are associated with denitrification, (ii) actinobacterial nitrate reducers and nirS-type and nosZ-harboring proteobacterial denitrifiers are important players, and (iii) acidic soils like palsa peats represent

  8. Excessive use of nitrogen in Chinese agriculture results in high N2O/(N2O+N2) product ratio of denitrification, primarily due to acidification of the soils

    PubMed Central

    Qu, Zhi; Wang, Jingguo; Almøy, Trygve; Bakken, Lars R

    2014-01-01

    China is the world's largest producer and consumer of fertilizer N, and decades of overuse has caused nitrate leaching and possibly soil acidification. We hypothesized that this would enhance the soils' propensity to emit N2O from denitrification by reducing the expression of the enzyme N2O reductase. We investigated this by standardized oxic/anoxic incubations of soils from five long-term fertilization experiments in different regions of China. After adjusting the nitrate concentration to 2 mM, we measured oxic respiration (R), potential denitrification (D), substrate-induced denitrification, and the denitrification product stoichiometry (NO, N2O, N2). Soils with a history of high fertilizer N levels had high N2O/(N2O+N2) ratios, but only in those field experiments where soil pH had been lowered by N fertilization. By comparing all soils, we found a strong negative correlation between pH and the N2O/(N2O+N2) product ratio (r2 = 0.759, P < 0.001). In contrast, the potential denitrification (D) was found to be a linear function of oxic respiration (R), and the ratio D/R was largely unaffected by soil pH. The immediate effect of liming acidified soils was lowered N2O/(N2O+N2) ratios. The results provide evidence that soil pH has a marginal direct effect on potential denitrification, but that it is the master variable controlling the percentage of denitrified N emitted as N2O. It has been known for long that low pH may result in high N2O/(N2O+N2) product ratios of denitrification, but our documentation of a pervasive pH-control of this ratio across soil types and management practices is new. The results are in good agreement with new understanding of how pH may interfere with the expression of N2O reductase. We argue that the management of soil pH should be high on the agenda for mitigating N2O emissions in the future, particularly for countries where ongoing intensification of plant production is likely to acidify the soils. PMID:24249526

  9. Modeling global annual N2O and NO emissions from fertilized fields

    NASA Astrophysics Data System (ADS)

    Bouwman, A. F.; Boumans, L. J. M.; Batjes, N. H.

    2002-12-01

    Information from 846 N2O emission measurements in agricultural fields and 99 measurements for NO emissions was used to describe the influence of various factors regulating emissions from mineral soils in models for calculating global N2O and NO emissions. Only those factors having a significant influence on N2O and NO emissions were included in the models. For N2O these were (1) environmental factors (climate, soil organic C content, soil texture, drainage and soil pH); (2) management-related factors (N application rate per fertilizer type, type of crop, with major differences between grass, legumes and other annual crops); and (3) factors related to the measurements (length of measurement period and frequency of measurements). The most important controls on NO emission include the N application rate per fertilizer type, soil organic-C content and soil drainage. Calculated global annual N2O-N and NO-N emissions from fertilized agricultural fields amount to 2.8 and 1.6 Mtonne, respectively. The global mean fertilizer-induced emissions for N2O and NO amount to 0.9% and 0.7%, respectively, of the N applied. These overall results account for the spatial variability of the main N2O and NO emission controls on the landscape scale.

  10. The O2 A-Band in the Fluxes and Polarization of Starlight Reflected by Earth-Like Exoplanets

    NASA Astrophysics Data System (ADS)

    Fauchez, Thomas; Rossi, Loic; Stam, Daphne M.

    2017-06-01

    Earth-like, potentially habitable exoplanets are prime targets in the search for extraterrestrial life. Information about their atmospheres and surfaces can be derived by analyzing the light of the parent star reflected by the planet. We investigate the influence of the surface albedo A s, the optical thickness b cloud, the altitude of water clouds, and the mixing ratio of biosignature O2 on the strength of the O2 A-band (around 760 nm) in the flux and polarization spectra of starlight reflected by Earth-like exoplanets. Our computations for horizontally homogeneous planets show that small mixing ratios (η < 0.4) will yield moderately deep bands in flux and moderate-to-small band strengths in polarization, and that clouds will usually decrease the band depth in flux and the band strength in polarization. However, cloud influence will be strongly dependent on properties such as optical thickness, top altitude, particle phase, coverage fraction, and horizontal distribution. Depending on the surface albedo and cloud properties, different O2 mixing ratios η can give similar absorption-band depths in flux and band strengths in polarization, especially if the clouds have moderate-to-high optical thicknesses. Measuring both the flux and the polarization is essential to reduce the degeneracies, although it will not solve them, especially not for horizontally inhomogeneous planets. Observations at a wide range of phase angles and with a high temporal resolution could help to derive cloud properties and, once those are known, the mixing ratio of O2 or any other absorbing gas.

  11. Noy -, N2o-, and O3-measurements In The Ut/ls-region During Spurt: Correlation-analyses and Implications For Transport and Mixing Processes

    NASA Astrophysics Data System (ADS)

    Hegglin, M.; Fischer, H.; Hoor, P.; Beuermann, J.; Brunner, D.; Peter, T.

    In the framework of SPURT we perform airborne in situ measurements of a variety of long-lived trace gases in order to investigate the role of dynamical and chemi- cal processes shaping the structure of the tropopause region. NOy is measured by chemiluminescence reaction of NO and O3, after reducing NOy species to NO by an externally mounted catalytic converter. N2O is measured by a Tunable Diode Laser Absorption Spectroscopy (TDLAS), O3 with help of an UV absorption photometer. Two short measurement campaigns were carried out with a Learjet in autumn 2001 and winter 2002. Individual flights were conducted in wide North-South cuts between 78 deg N (Spitzbergen) and 28 deg S (Tenerife). In this contribution, first results will be presented including observations obtained from a flight through a spectacularly deep stratospheric intrusion with potentially significant troposphere/stratosphere ex- change. The effect of the STE on tracer-tracer correlations such as NOy-O3, O3-N2O, and NOy-N2O will be evaluated. The results will be compared with known correla- tions and also with analyses of backward-trajectories, showing the strong influence of air mass origin on the correlations obtained.

  12. New observations of stratospheric N2O5

    NASA Technical Reports Server (NTRS)

    Rinsland, C. P.; Toon, G. C.; Farmer, C. B.; Norton, R. H.; Namkung, J. S.

    1989-01-01

    The unequivocal detection of N2O5 in the stratosphere was reported by Toon et al. based on measurements of the absorption by the N2O5 bands at 1246 and 1720/cm in solar occulation spectra recorded at sunrise near 47 S latitude by the Atmospheric Trace Molecule Spectroscopy (ATMOS) experiment during the Spacelab 3 (SL3) shuttle mission. Additional measurements and analysis of stratospheric N2O5 derived from the ATMOS/SL3 spectra are reported. The primary results are the detection and measurement of N2O5 absorption at sunset in the lower stratosphere, the inversion of a precise (approximately 10 percent) N2O5 sunrise vertical distribution between 25.5 and 37.5 km altitude, and the identification and measurement of absorption by the N2O5 743/cm band at sunrise. Assuming 4.32 x 10(sup -17) and 4.36 x 10(sup -17)/cm/molecule/sq cm respectively for the integrated intensities of the 1246 and 743/cm bands at stratospheric temperatures, retrieved volume mixing ratios in parts per billion by volume (ppbv) at sunrise (47 S latitude) are 1.32 + or - 0.34 at 37.5 km, 1.53 + or - 0.35 at 35.5 km, 1.63 + or - 0.36 at 33.5 km, 1.60 + or - 0.34 at 31.5 km, 1.43 + or - 0.30 at 29.5 km, 1.15 + or - 0.24 at 27.5 km, and 0.73 + or - 0.15 at 25.5 km. Retrieved VMRs in ppbv at sunset (30 N latitude) are 0.13 + or - 0.05 at 29.5 km, 0.14 + or - 0.05 at 27.5 km, and 0.10 + or - 0.04 at 25.5 km. Quoted error limits (1 sigma) include the error in the assumed band intensities (approximately 20 percent). Within the error limits of the measurements, the inferred mixing ratios at sunrise agree with diurnal photochemical model predictions obtained by two groups using current photochemical data. The measured mixing ratios at sunset are lower than the model predictions with differences of about a factor of 2 at 25 km altitude.

  13. Response of CO2 and H2O fluxes of a mountainous tropical rain forest in equatorial Indonesia to El Niño events

    NASA Astrophysics Data System (ADS)

    Olchev, A.; Ibrom, A.; Panferov, O.; Gushchina, D.; Propastin, P.; Kreilein, H.; June, T.; Rauf, A.; Gravenhorst, G.; Knohl, A.

    2015-03-01

    The possible impact of El Niño-Southern Oscillation (ENSO) events on the main components of CO2 and H2O fluxes in a pristine mountainous tropical rainforest growing in Central Sulawesi in Indonesia is described. The fluxes were continuously measured using the eddy covariance method for the period from January 2004 to June 2008. During this period, two episodes of El Niño and one episode of La Niña were observed. All these ENSO episodes had moderate intensity and were of Central Pacific type. The temporal variability analysis of the main meteorological parameters and components of CO2 and H2O exchange showed a very high sensitivity of Evapotranspiration (ET) and Gross Primary Production (GPP) of the tropical rain forest to meteorological variations caused by both El Niño and La Niña episodes. Incoming solar radiation is the main governing factor that is responsible for ET and GPP variability. Ecosystem Respiration (RE) dynamics depend mainly on the air temperature changes and are almost insensitive to ENSO. Changes of precipitation due to moderate ENSO events did not cause any notable effect on ET and GPP, mainly because of sufficient soil moisture conditions even in periods of anomalous reduction of precipitation in the region.

  14. The correlation between HCN/H2O flux ratios and disk mass: evidence for protoplanet formation

    NASA Astrophysics Data System (ADS)

    Rose, Caitlin; Salyk, Colette

    2017-01-01

    We analyze hydrogen cyanide (HCN) and water vapor flux ratios in protoplanetary disks as a way to trace planet formation. Analyzing only disks in the Taurus molecular cloud, Najita et al. (2013) found a tentative correlation between protoplanetary disk mass and the HCN/H2O line flux ratio in Spitzer-IRS emission spectra. They interpret this correlation to be a consequence of more massive disks forming planetesimals more efficiently than smaller disks, as the formation of large planetesimals may lock up water ice in the cool outer disk region and prevent it from migrating, drying out the inner disk. The sequestering of water (and therefore oxygen) in the outer disk may also increase the carbon-to- oxygen ratio in the inner disk, leading to enhanced organic molecule (e.g. HCN) emission. To confirm this trend, we expand the Najita et al. sample by calculating HCN/H2O line flux ratios for 8 more sources with known disk masses from clusters besides Taurus. We find agreement with the Najita et al. trend, suggesting that this is a widespread phenomenon. In addition, we find HCN/H2O line flux ratios for 17 more sources that await disk mass measurements, which should become commonplace in the ALMA era. Finally, we investigate linear fits and outliers to this trend, and discuss possible causes.

  15. N2O vibration-rotation parameters derived from measurements in the 900-1090- and 1580-2380/cm regions

    NASA Technical Reports Server (NTRS)

    Toth, Robert A.

    1987-01-01

    Fourier-transform spectrometric measurements of the N2O IR spectrum in the 900-1090 and 1580-2380/cm regions were obtained at a 0.005/cm resolution, and line frequencies of eight species for several ground state bands and hot bands are analyzed to obtain values of band centers and upper-state effective rotational constants. Several bands are reported for the first time. Least-squares fits for the 0400-0000, 0420(e)-0000, and 0510-0110 bands of the (N-14)2O-16 species suggest perturbation of the high-J levels of the upper states. Resonance interactions were noted in transitions including the 1001-1000 bands of (N-14)2O-16 and N-15N-14O-16.

  16. Actinometric measurements and theoretical calculations of j/O3/, the rate of photolysis of ozone to O/1D/

    NASA Technical Reports Server (NTRS)

    Dickerson, R. R.; Stedman, D. H.; Chameides, W. L.; Crutzen, P. J.; Fishman, J.

    1979-01-01

    The paper presents an experimental technique which measures j/O3-O(1-D)/, the rate of solar photolysis of ozone to singlet oxygen atoms. It is shown that a flow actinometer carries dilute O3 in N2O into direct sunlight where the O(1D) formed reacts with N2O to form NO which chemiluminescence detects, with a time resolution of about one minute. Measurements indicate a photolysis rate of 1.2 (+ or - .2) x 10 to the -5/s for a cloudless sky, 45 deg zenith angle, 0.345 cm ozone column and zero albedo. Finally, ground level results compare with theoretical calculations based on the UV actinic flux as a function of ozone column and solar zenith angle.

  17. Vertical profiles of ClNO2 measured in Utah: dry deposition of N2O5 as a source of ClNO2

    NASA Astrophysics Data System (ADS)

    McLaren, Robert; Roberts, James M.; Kercher, James P.; Thornton, Joel A.; Brown, Steven S.; Edwards, Peter M.; Young, Cora Y.; Dube, William P.; Washenfelder, Rebecca A.; Williams, Eric J.; Holloway, John S.; Bates, Timothy S.; Quinn, Patricia K.

    2013-04-01

    Several recent observations of nitryl chloride (ClNO2) have suggested that this compound can accumulate to significant levels (several ppb) in the nocturnal boundary layer at night. Its photolytic loss the next day can be a significant source of chlorine atom radicals. The source of ClNO2 is known to be the heterogeneous reaction of N2O5 with aerosol chloride, not just confined to coastal regions but also observed thousands of kilometers inland in urban areas. During the Uintah Basin Winter Ozone Study (2012), we made measurements of ClNO2 by CIMS on a tower in a remote region of Utah where intensive natural gas extraction operations via hydraulic fracturing were occurring. Levels of ClNO2 were surprisingly high at night (up to 2 ppb) even though coastal aerosols were not present. Soils in the region were alkaline with high chloride content. To address the potential of N2O5 dry deposition as a source of ClNO2, we measured vertical profiles of ClNO2 from 1 to 12 m agl with a movable inlet. We observed negative gradients of ClNO2 and positive gradients of N2O5, which suggest that dry deposition of N2O5 and reaction with soil chloride as a source of ClNO2.

  18. Electrical characteristics of proton-irradiated Sc2O3 passivated AlGaN/GaN high electron mobility transistors

    NASA Astrophysics Data System (ADS)

    Luo, B.; Kim, Jihyun; Ren, F.; Gillespie, J. K.; Fitch, R. C.; Sewell, J.; Dettmer, R.; Via, G. D.; Crespo, A.; Jenkins, T. J.; Gila, B. P.; Onstine, A. H.; Allums, K. K.; Abernathy, C. R.; Pearton, S. J.; Dwivedi, R.; Fogarty, T. N.; Wilkins, R.

    2003-03-01

    Sc2O3-passivated AlGaN/GaN high electron mobility transistors (HEMTs) were irradiated with 40 MeV protons to a fluence corresponding to approximately 10 years in low-earth orbit (5×109 cm-2). Devices with an AlGaN cap layer showed less degradation in dc characteristics than comparable GaN-cap devices, consistent with differences in average band energy. The changes in device performance could be attributed completely to bulk trapping effects, demonstrating that the effectiveness of the Sc2O3 layers in passivating surface states in the drain-source region was undiminished by the proton irradiation. Sc2O3-passivated AlGaN/HEMTs appear to be attractive candidates for space and terrestrial applications where resistance to high fluxes of ionizing radiation is a criteria.

  19. A Reaction Between High Mn-High Al Steel and CaO-SiO2-Type Molten Mold Flux: Part II. Reaction Mechanism, Interface Morphology, and Al2O3 Accumulation in Molten Mold Flux

    NASA Astrophysics Data System (ADS)

    Kang, Youn-Bae; Kim, Min-Su; Lee, Su-Wan; Cho, Jung-Wook; Park, Min-Seok; Lee, Hae-Geon

    2013-04-01

    Following a series of laboratory-scale experiments, the mechanism of a chemical reaction 4[{Al}] + 3({SiO}_2) = 3[{Si}] + 2({Al}_2{O}_3) between high-alloyed TWIP (TWin-Induced Plasticity) steel containing Mn and Al and molten mold flux composed mainly of CaO-SiO2 during the continuous casting process is discussed in the present article in the context of kinetic analysis, morphological evolution at the reaction interface. By the kinetic analysis using a two-film theory, a rate-controlling step of the chemical reaction at the interface between the molten steel and the molten flux is found to be mass transport of Al in a boundary layer of the molten steel, as long as the molten steel and the molten flux phases are concerned. Mass transfer coefficient of the Al in the boundary layer (k_{{Al}}) is estimated to be 0.9 to 1.2 × 10-4 m/s at 1773 K (1500 ^{circ}C). By utilizing experimental data at various temperatures, the following equation is obtained for the k_{{Al}}; ln k_{{Al}} = -14,290/T - 1.1107. Activation energy for the mass transfer of Al in the boundary layer is 119 kJ/mol, which is close to a value of activation energy for mass transfer in metal phase. The composition evolution of Al in the molten steel was well explained by the mechanism of Al mass transfer. On the other hand, when the concentration of Al in the steel was high, a significant deviation of the composition evolution of Al in the molten steel was observed. By observing reaction interface between the molten steel and the molten flux, it is thought that the chemical reaction controlled by the mass transfer of Al seemed to be disturbed by formation of a solid product layer of MgAl2O4. A model based on a dynamic mass balance and the reaction mechanism of mass transfer of Al in the boundary layer for the low Al steel was developed to predict (pct Al2O3) accumulation rate in the molten mold flux.

  20. Active nitrogen partitioning and the nighttime formation of N sub 2 O sub 5 in the stratosphere: Simultaneous in situ measurements of NO, NO sub 2 , HNO sub 3 , O sub 3 , and N sub 2 O using the BLISS diode laser spectrometer

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    Webster, C.R.; May, R.D.; Toumi, R.

    1990-08-20

    Simultaneous in situ measurements of NO, NO{sub 2}, HNO{sub 3}, O{sub 3}, N{sub 2}O, pressure, and temperature at 30 km have been made from Palestine. Texas (32{degree}N) on September 13, 1988, using the Jet Propulsion Laboratory Balloon-Borne Laser In-Situ Sensor (BLISS) instrument, with the NOAA dual-channel balloon UV ozone spectrometer on the same gondola. Using tunable diode laser absorption spectroscopy over a long path length, measurements were made during a 24-hour flight of the daytime concentrations of NO, NO{sub 2}, and O{sub 3} and of the diurnal variation in the concentration of NO{sub 2}. Postsunset measurements of NO{sub 2}, mademore » every half minutes throughout much of the night, show the NO{sub 2} mixing ratio falling from a sunset value of 10.5 ppbv to 5.2 ppbv at nights end. From the sunset/sunrise difference din the volume mixing ratio of NO{sub 2} is derived a value of 2.7 {plus minus} 0.4 ppbv for the sunrise N{sub 2}O{sub 5} mixing ratio, in excellent agreement with the model predictions of 2.9 ppbv at this latitude. The measured daytime NO{sub 2}/NO ratio was found to be in good agreement with model predictions at 30 km. The measured presunset sum NO + NO{sub 2} of 10.1 {plus minus} 0.8 ppbv agreed well with the measured postsunset NO{sub 2} amount of 10.5 {plus minus} 0.8 ppbv. Simultaneous measurements of the mixing ratios of HNO{sub 3} and postsunset NO{sub 2} allow an estimate of total reactive nitrogen, approximated at this time by NO{sub 2} + HNO{sub 3} + 2(N{sub 2}O{sub 5}) + ClONO{sub 2}, of 16.4 {plus minus} 1.2 ppbv at 30 km, and (from an earlier flight) of 13.7 {plus minus} 1.7 ppbv at 37 km. Using model predictions incorporating corrections for non-steady state and for diurnal chemistry, an OH mixing ratio of 8 {plus minus} 4 pptv is derived from the measured HNO{sub 3}/NO{sub 2} ratio of 0.72 {plus minus} 0.17 at 30 km.« less

  1. Gross nitrous oxide production drives net nitrous oxide fluxes across a salt marsh landscape.

    PubMed

    Yang, Wendy H; Silver, Whendee L

    2016-06-01

    Sea level rise will change inundation regimes in salt marshes, altering redox dynamics that control nitrification - a potential source of the potent greenhouse gas, nitrous oxide (N2 O) - and denitrification, a major nitrogen (N) loss pathway in coastal ecosystems and both a source and sink of N2 O. Measurements of net N2 O fluxes alone yield little insight into the different effects of redox conditions on N2 O production and consumption. We used in situ measurements of gross N2 O fluxes across a salt marsh elevation gradient to determine how soil N2 O emissions in coastal ecosystems may respond to future sea level rise. Soil redox declined as marsh elevation decreased, with lower soil nitrate and higher ferrous iron in the low marsh compared to the mid and high marshes (P < 0.001 for both). In addition, soil oxygen concentrations were lower in the low and mid-marshes relative to the high marsh (P < 0.001). Net N2 O fluxes differed significantly among marsh zones (P = 0.009), averaging 9.8 ± 5.4 μg N m(-2)  h(-1) , -2.2 ± 0.9 μg N m(-2)  h(-1) , and 0.67 ± 0.57 μg N m(-2)  h(-1) in the low, mid, and high marshes, respectively. Both net N2 O release and uptake were observed in the low and high marshes, but the mid-marsh was consistently a net N2 O sink. Gross N2 O production was highest in the low marsh and lowest in the mid-marsh (P = 0.02), whereas gross N2 O consumption did not differ among marsh zones. Thus, variability in gross N2 O production rates drove the differences in net N2 O flux among marsh zones. Our results suggest that future studies should focus on elucidating controls on the processes producing, rather than consuming, N2 O in salt marshes to improve our predictions of changes in net N2 O fluxes caused by future sea level rise. © 2015 John Wiley & Sons Ltd.

  2. New ground-based lidar enables volcanic CO2 flux measurements.

    PubMed

    Aiuppa, Alessandro; Fiorani, Luca; Santoro, Simone; Parracino, Stefano; Nuvoli, Marcello; Chiodini, Giovanni; Minopoli, Carmine; Tamburello, Giancarlo

    2015-09-01

    There have been substantial advances in the ability to monitor the activity of hazardous volcanoes in recent decades. However, obtaining early warning of eruptions remains challenging, because the patterns and consequences of volcanic unrests are both complex and nonlinear. Measuring volcanic gases has long been a key aspect of volcano monitoring since these mobile fluids should reach the surface long before the magma. There has been considerable progress in methods for remote and in-situ gas sensing, but measuring the flux of volcanic CO2-the most reliable gas precursor to an eruption-has remained a challenge. Here we report on the first direct quantitative measurements of the volcanic CO2 flux using a newly designed differential absorption lidar (DIAL), which were performed at the restless Campi Flegrei volcano. We show that DIAL makes it possible to remotely obtain volcanic CO2 flux time series with a high temporal resolution (tens of minutes) and accuracy (<30%). The ability of this lidar to remotely sense volcanic CO2 represents a major step forward in volcano monitoring, and will contribute improved volcanic CO2 flux inventories. Our results also demonstrate the unusually strong degassing behavior of Campi Flegrei fumaroles in the current ongoing state of unrest.

  3. Development of an atmospheric N2O isotopocule model and optimization procedure, and application to source estimation

    NASA Astrophysics Data System (ADS)

    Ishijima, K.; Takigawa, M.; Sudo, K.; Toyoda, S.; Yoshida, N.; Röckmann, T.; Kaiser, J.; Aoki, S.; Morimoto, S.; Sugawara, S.; Nakazawa, T.

    2015-07-01

    This paper presents the development of an atmospheric N2O isotopocule model based on a chemistry-coupled atmospheric general circulation model (ACTM). We also describe a simple method to optimize the model and present its use in estimating the isotopic signatures of surface sources at the hemispheric scale. Data obtained from ground-based observations, measurements of firn air, and balloon and aircraft flights were used to optimize the long-term trends, interhemispheric gradients, and photolytic fractionation, respectively, in the model. This optimization successfully reproduced realistic spatial and temporal variations of atmospheric N2O isotopocules throughout the atmosphere from the surface to the stratosphere. The very small gradients associated with vertical profiles through the troposphere and the latitudinal and vertical distributions within each hemisphere were also reasonably simulated. The results of the isotopic characterization of the global total sources were generally consistent with previous one-box model estimates, indicating that the observed atmospheric trend is the dominant factor controlling the source isotopic signature. However, hemispheric estimates were different from those generated by a previous two-box model study, mainly due to the model accounting for the interhemispheric transport and latitudinal and vertical distributions of tropospheric N2O isotopocules. Comparisons of time series of atmospheric N2O isotopocule ratios between our model and observational data from several laboratories revealed the need for a more systematic and elaborate intercalibration of the standard scales used in N2O isotopic measurements in order to capture a more complete and precise picture of the temporal and spatial variations in atmospheric N2O isotopocule ratios. This study highlights the possibility that inverse estimation of surface N2O fluxes, including the isotopic information as additional constraints, could be realized.

  4. Development of an atmospheric N2O isotopocule model and optimization procedure, and application to source estimation

    NASA Astrophysics Data System (ADS)

    Ishijima, K.; Takigawa, M.; Sudo, K.; Toyoda, S.; Yoshida, N.; Röckmann, T.; Kaiser, J.; Aoki, S.; Morimoto, S.; Sugawara, S.; Nakazawa, T.

    2015-12-01

    This work presents the development of an atmospheric N2O isotopocule model based on a chemistry-coupled atmospheric general circulation model (ACTM). We also describe a simple method to optimize the model and present its use in estimating the isotopic signatures of surface sources at the hemispheric scale. Data obtained from ground-based observations, measurements of firn air, and balloon and aircraft flights were used to optimize the long-term trends, interhemispheric gradients, and photolytic fractionation, respectively, in the model. This optimization successfully reproduced realistic spatial and temporal variations of atmospheric N2O isotopocules throughout the atmosphere from the surface to the stratosphere. The very small gradients associated with vertical profiles through the troposphere and the latitudinal and vertical distributions within each hemisphere were also reasonably simulated. The results of the isotopic characterization of the global total sources were generally consistent with previous one-box model estimates, indicating that the observed atmospheric trend is the dominant factor controlling the source isotopic signature. However, hemispheric estimates were different from those generated by a previous two-box model study, mainly due to the model accounting for the interhemispheric transport and latitudinal and vertical distributions of tropospheric N2O isotopocules. Comparisons of time series of atmospheric N2O isotopocule ratios between our model and observational data from several laboratories revealed the need for a more systematic and elaborate intercalibration of the standard scales used in N2O isotopic measurements in order to capture a more complete and precise picture of the temporal and spatial variations in atmospheric N2O isotopocule ratios. This study highlights the possibility that inverse estimation of surface N2O fluxes, including the isotopic information as additional constraints, could be realized.

  5. Nitrous oxide fluxes from a commercial beef cattle feedlot in Kansas

    USDA-ARS?s Scientific Manuscript database

    Emission of greenhouse gases, including nitrous oxide (N2O), from open beef cattle feedlots is becoming an environmental concern; however, research measuring emission rates of N2O from open beef cattle feedlots has been limited. This study was conducted to quantify N2O emission fluxes as affected by...

  6. Simulation of atmospheric N2O with GEOS-Chem and its adjoint: evaluation of observational constraints

    NASA Astrophysics Data System (ADS)

    Wells, K. C.; Millet, D. B.; Bousserez, N.; Henze, D. K.; Chaliyakunnel, S.; Griffis, T. J.; Luan, Y.; Dlugokencky, E. J.; Prinn, R. G.; O'Doherty, S.; Weiss, R. F.; Dutton, G. S.; Elkins, J. W.; Krummel, P. B.; Langenfelds, R.; Steele, L. P.; Kort, E. A.; Wofsy, S. C.; Umezawa, T.

    2015-10-01

    We describe a new 4D-Var inversion framework for nitrous oxide (N2O) based on the GEOS-Chem chemical transport model and its adjoint, and apply it in a series of observing system simulation experiments to assess how well N2O sources and sinks can be constrained by the current global observing network. The employed measurement ensemble includes approximately weekly and quasi-continuous N2O measurements (hourly averages used) from several long-term monitoring networks, N2O measurements collected from discrete air samples onboard a commercial aircraft (Civil Aircraft for the Regular Investigation of the atmosphere Based on an Instrument Container; CARIBIC), and quasi-continuous measurements from the airborne HIAPER Pole-to-Pole Observations (HIPPO) campaigns. For a 2-year inversion, we find that the surface and HIPPO observations can accurately resolve a uniform bias in emissions during the first year; CARIBIC data provide a somewhat weaker constraint. Variable emission errors are much more difficult to resolve given the long lifetime of N2O, and major parts of the world lack significant constraints on the seasonal cycle of fluxes. Current observations can largely correct a global bias in the stratospheric sink of N2O if emissions are known, but do not provide information on the temporal and spatial distribution of the sink. However, for the more realistic scenario where source and sink are both uncertain, we find that simultaneously optimizing both would require unrealistically small errors in model transport. Regardless, a bias in the magnitude of the N2O sink would not affect the a posteriori N2O emissions for the 2-year timescale used here, given realistic initial conditions, due to the timescale required for stratosphere-troposphere exchange (STE). The same does not apply to model errors in the rate of STE itself, which we show exerts a larger influence on the tropospheric burden of N2O than does the chemical loss rate over short (< 3 year) timescales. We use a

  7. Portable Automation of Static Chamber Sample Collection for Quantifying Soil Gas Flux

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    Davis, Morgan P.; Groh, Tyler A.; Parkin, Timothy B.

    Quantification of soil gas flux using the static chamber method is labor intensive. The number of chambers that can be sampled is limited by the spacing between chambers and the availability of trained research technicians. An automated system for collecting gas samples from chambers in the field would eliminate the need for personnel to return to the chamber during a flux measurement period and would allow a single technician to sample multiple chambers simultaneously. This study describes Chamber Automated Sampling Equipment (FluxCASE) to collect and store chamber headspace gas samples at assigned time points for the measurement of soil gasmore » flux. The FluxCASE design and operation is described, and the accuracy and precision of the FluxCASE system is evaluated. In laboratory measurements of nitrous oxide (N2O), carbon dioxide (CO2), and methane (CH4) concentrations of a standardized gas mixture, coefficients of variation associated with automated and manual sample collection were comparable, indicating no loss of precision. In the field, soil gas fluxes measured from FluxCASEs were in agreement with manual sampling for both N2O and CO2. Slopes of regression equations were 1.01 for CO2 and 0.97 for N2O. The 95% confidence limits of the slopes of the regression lines included the value of one, indicating no bias. Additionally, an expense analysis found a cost recovery ranging from 0.6 to 2.2 yr. Implementing the FluxCASE system is an alternative to improve the efficiency of the static chamber method for measuring soil gas flux while maintaining the accuracy and precision of manual sampling.« less

  8. Ecological Controls on N2O Emission in Surface Litter and Near-surface Soil of a Managed Grassland: Modelling and Measurements

    NASA Astrophysics Data System (ADS)

    Grant, Robert; Neftel, Albrecht; Calanca, Pierluigi

    2016-04-01

    Large variability in N2O emissions from managed grasslands may occur because most emissions originate in surface litter or near-surface soil where variability in soil water content (q) and temperature (Ts) is greatest. To determine whether temporal variability in q and Ts of surface litter and near-surface soil could explain that in N2O emissions, a simulation experiment was conducted with ecosys, a comprehensive mathematical model of terrestrial ecosystems in which processes governing N2O emissions were represented at high temporal and spatial resolution. Model performance was verified by comparing N2O emissions, CO2 and energy exchange, and q and Ts modelled by ecosys with those measured by automated chambers, eddy covariance (EC) and soil sensors at an hourly time-scale during several emission events from 2004 to 2009 in an intensively managed pasture at Oensingen, Switzerland. Both modelled and measured events were induced by precipitation following harvesting and subsequent fertilizing or manuring. These events were brief (2 - 5 days) with maximum N2O effluxes that varied from < 1 mg N m-2 h-1 in early spring and autumn to > 3 mg N m-2 h-1 in summer. Only very small emissions were modelled or measured outside these events. In the model, emissions were generated almost entirely in surface litter or near-surface (0 - 2 cm) soil, at rates driven by N availability with fertilization vs. N uptake with grassland regrowth, and by O2 limitation from wetting relative to O2 demand from respiration. In the model, NOx availability relative to O2 limitation governed both the reduction of more oxidized electron acceptors to N2O and the reduction of N2O to N2, so that the magnitude of N2O emissions was not simply related to surface and near-surface q and Ts. Modelled N2O emissions were found to be sensitive to defoliation intensity and timing (relative to that of fertilization) which controlled plant N uptake and soil q and Ts prior to and during emission events. In a model

  9. Nitrification and N2O production processes in soil incubations after ammonium fertilizer application at high concentrations

    NASA Astrophysics Data System (ADS)

    Deppe, Marianna; Well, Reinhard; Giesemann, Anette; Flessa, Heinz

    2016-04-01

    High concentrations of ammonium as they occur, e.g., after point-injection of ammonium fertilizer solution according to the CULTAN fertilization technique may retard nitrification. Potential advantages in comparison to conventional fertilization include a higher N efficiency of crops, reduced nitrate leaching, and lower N2O and N2 emissions. Dynamics of nitrification due to plant uptake and dilution processes, leading to decreasing ammonium concentrations in fertilizer depots, has only poorly been studied before. Furthermore, there is little information about the relative contribution of different N2O production processes under these conditions. To elucidate the process dynamics a laboratory incubation study was conducted. After fertilization with ammonium sulfate at 5 levels (from 0 to 5000 mg NH4+-N kg-1; 20mg NO3--N kg-1 each), sandy loam soil was incubated in dynamic soil microcosms for 21 days. N2O, CH4 and CO2 fluxes as well as isotope signatures of N2O and, at three dates, NO3- and NH4+ were measured. To identify N2O production processes, acetylene inhibition (0.01 vol.%), 15N tracer approaches, and isotopomer data (15N site preference and δ18O) were used. N2O emissions were highest at 450mg NH4+-N kg-1 and declined with further increasing concentrations. At 5000 mg NH4+-N kg-1 nitrification was completely inhibited. However, approximately 90% of N2O production was inhibited by acetylene application, and there was no change in the relative contribution of nitrification and denitrification to N2O production with N level. Applying the non-equilibrium technique to our 15N tracer data revealed heterogeneous distribution of denitrification in soil, with at least two distinct NO3- pools, and spatial separation of NO3- formation and consumption. In comparison with the acetylene inhibition and 15N tracer approaches the results of the isotopomer approach were reasonable and indicated substantial contribution of nitrifier-denitrification (10-40%) to total N2O

  10. A digital wide range neutron flux measuring system for HL-2A

    NASA Astrophysics Data System (ADS)

    Yuan, Chen; Wu, Jun; Yin, Zejie

    2017-08-01

    To achieve wide-range, high-integration, and real-time performance on the neutron flux measurement on the HL-2A tokamak, a digital neutron flux measuring (DNFM) system based on the peripheral component interconnection (PCI) eXtension for Instrumentation express (PXIe) bus was designed. This system comprises a charge-sensitive preamplifier and a field programmable gate array (FPGA)-based main electronics plug-in. The DNFM totally covers source-range and intermediate-range neutron flux measurements, and increases system integration by a large margin through joining the pulse-counting mode and Campbell mode. Meanwhile, the neutron flux estimation method based on pulse piling proportions is able to choose and switch measuring modes in accordance with current flux, and this ensures the accuracy of measurements when the neutron flux changes suddenly. It has been demonstrated by simulated signals that the DNFM enhances the full-scale measuring range up to 1.9 × 108 cm-2 s-1, with relative error below 6.1%. The DNFM has been verified to provide a high temporal sensitivity at 10 ms time intervals on a single fission chamber on HL-2A. Contributed paper, published as part of the Proceedings of the 3rd Domestic Electromagnetic Plasma Diagnostics Workshop, September 2016, Hefei, China.

  11. Riverine N2O concentrations, exports to estuary and emissions to atmosphere from the Changjiang River in response to increasing nitrogen loads

    NASA Astrophysics Data System (ADS)

    Yan, Weijin; Yang, Libiao; Wang, Fang; Wang, Jianing; Ma, Pei

    2012-12-01

    This study investigated the variations of dissolved N2O and emissions over diurnal and seasonal temporal scales in 2009, as well as the time series of riverine N2O export to estuary and emission to atmosphere in response to increasing anthropogenic nitrogen loads in the Changjiang River. For the diurnal study, N2O concentrations ranged from 0.26 to 0.34 and from 0.44 to 0.52 μg N-N2O L-1 in August and October 2009, respectively. The dissolved N2O was supersaturated with a mean value of 197%. Studies on N2O emissions, also taken in August and October, ranged from 2.67 to 11.6 and from 6.72 to 15.2 μg N-N2O m-2 h-1, respectively. For the seasonal study (June through December 2009), N2O concentrations ranged from 0.34 to 0.72 μg N-N2O L-1 and were supersaturated in all the samples (average 212%). N2O emissions ranged from 1.87 to 40.8 μg N-N2O m-2 h-1. Our study found no significant differences in diurnal patterns of N2O saturation but detected significant difference in seasonal patterns of N2O saturation: higher during summer while lower during autumn and winter. We found a significant relationship between dissolved N2O and river nitrate, which can predict the variation of N2O concentrations in the River. The net production of N2 ranged from 0.01 to 0.47 mg N-N2 L-1. These excess N2 values were significantly correlated to the N2O production and are suggestive of denitrification in the river. Applying the Global News model to the river system using measures taken during the 1970 to 2002 period, we estimated N2O emissions to atmosphere increased from 330 to 3650 ton N-N2O yr-1. During that same 1970-2002 period, N2O exports to estuary increased from 91 to 470 ton N-N2O yr-1. Taken together, the findings reported here suggest that both the river N2O concentrations and emissions would increase in response to rising anthropogenic nitrogen loads. Our study showed that the mean emission factor based on the ratio of the total N2O flux to NO3- flux is four times greater

  12. Effects of carbon sources and COD/N ratio on N2O emissions in subsurface flow constructed wetlands.

    PubMed

    Lyu, Wanlin; Huang, Lei; Xiao, Guangquan; Chen, Yucheng

    2017-12-01

    A set of constructed wetlands under two different carbon sources, namely, glucose (CW) and sodium acetate (YW), was established at a laboratory scale with influent COD/N ratios of 20:1, 10:1, 7:1, 4:1, and 0 to analyze the influence of carbon supply on nitrous oxide emissions. Results showed that the glucose systems generated higher N 2 O emissions than those of the sodium acetate systems. The higher amount of N 2 O-releasing fluxes in the CWs than in the YWs was consistent with the higher NO 2 - -N accumulation in the former than in the latter. Moreover, electron competition was tighter in the CWs and contributed to the incomplete denitrification with poor N 2 O production performance. Illumina MiSeq sequencing demonstrated that some denitrifying bacteria, such as Denitratisoma, Bacillus, and Zoogloea, were higher in the YWs than in the CWs. This result indicated that the carbon source is important in controlling N 2 O emissions in microbial communities. Copyright © 2017. Published by Elsevier Ltd.

  13. Comparison of the Microstructure and Flux Pinning Properties of Polycrystalline YBa2Cu3O7-d Containing Zn0.95Mn0.05O or Al2O3 Nanoparticles

    NASA Astrophysics Data System (ADS)

    Al-Mohsin, R. A.; Al-Otaibi, A. L.; Almessiere, M. A.; Al-badairy, H.; Slimani, Y.; Ben Azzouz, F.

    2018-07-01

    Here we compare the microstructure and flux pinning properties of polycrystalline YBa2Cu3O7-d (Y-123 or YBCO) containing either Al2O3 or Zn0.95Mn0.05O nanoparticles. Samples were prepared using a standard solid-state reaction process, and nanoparticles were added up to a concentration of 0.1 wt%. The crystal structure, microstructure, electrical and magnetic properties were analyzed using X-ray diffraction, scanning electron microscopy and transmission electron microscopy (TEM), and electrical resistivity and DC magnetization measurements, respectively. TEM observations showed that the addition of Zn0.95Mn0.05O resulted in a high density of fine twins and a variety of interacting microstructures, while Al2O3 addition resulted in a high density of Al-rich nanoscale inhomogeneities embedded in the Y-123 matrix. Flux pinning forces were determined, and predominant pinning mechanisms in the prepared samples were proposed. We evaluated the superconducting properties of YBCO considering the effects of adding insulating or magnetic nanoparticles.

  14. Comparison of the Microstructure and Flux Pinning Properties of Polycrystalline YBa2Cu3O7-d Containing Zn0.95Mn0.05O or Al2O3 Nanoparticles

    NASA Astrophysics Data System (ADS)

    Al-Mohsin, R. A.; Al-Otaibi, A. L.; Almessiere, M. A.; Al-badairy, H.; Slimani, Y.; Ben Azzouz, F.

    2018-03-01

    Here we compare the microstructure and flux pinning properties of polycrystalline YBa2Cu3O7-d (Y-123 or YBCO) containing either Al2O3 or Zn0.95Mn0.05O nanoparticles. Samples were prepared using a standard solid-state reaction process, and nanoparticles were added up to a concentration of 0.1 wt%. The crystal structure, microstructure, electrical and magnetic properties were analyzed using X-ray diffraction, scanning electron microscopy and transmission electron microscopy (TEM), and electrical resistivity and DC magnetization measurements, respectively. TEM observations showed that the addition of Zn0.95Mn0.05O resulted in a high density of fine twins and a variety of interacting microstructures, while Al2O3 addition resulted in a high density of Al-rich nanoscale inhomogeneities embedded in the Y-123 matrix. Flux pinning forces were determined, and predominant pinning mechanisms in the prepared samples were proposed. We evaluated the superconducting properties of YBCO considering the effects of adding insulating or magnetic nanoparticles.

  15. Soil N2O and NO emissions from land use and land-use change in the tropics and subtropics: a meta-analysis

    NASA Astrophysics Data System (ADS)

    van Lent, J.; Hergoualc'h, K.; Verchot, L. V.

    2015-08-01

    Deforestation and forest degradation in the tropics may substantially alter soil N-oxide emissions. It is particularly relevant to accurately quantify those changes to properly account for them in a REDD+ climate change mitigation scheme that provides financial incentives to reduce the emissions. With this study we provide updated land use (LU)-based emission rates (103 studies, 387 N2O and 111 NO case studies), determine the trend and magnitude of flux changes with land-use change (LUC) using a meta-analysis approach (43 studies, 132 N2O and 37 NO cases) and evaluate biophysical drivers of N2O and NO emissions and emission changes for the tropics. The average N2O and NO emissions in intact upland tropical forest amounted to 2.0 ± 0.2 (n = 88) and 1.7 ± 0.5 (n = 36) kg N ha-1 yr-1, respectively. In agricultural soils annual N2O emissions were exponentially related to N fertilization rates and average water-filled pore space (WFPS) whereas in non-agricultural sites a Gaussian response to WFPS fit better the observed NO and N2O emissions. The sum of soil N2O and NO fluxes and the ratio of N2O to NO increased exponentially and significantly with increasing nitrogen availability (expressed as NO3-/[NO3-+NH4+]) and WFPS, respectively; following the conceptual Hole-In-the-Pipe model. Nitrous and nitric oxide fluxes did not overall increase significantly as a result of LUC (Hedges's d of 0.11 ± 0.11 and 0.16 ± 0.19, respectively), however individual LUC trajectories or practices did. Nitrous oxide fluxes increased significantly after intact upland forest conversion to croplands (Hedges's d = 0.78 ± 0.24) and NO increased significantly following the conversion of low forest cover (secondary forest younger than 30 years, woodlands, shrublands) (Hedges's d of 0.44 ± 0.13). Forest conversion to fertilized systems significantly and highly raised both N2O and NO emission rates (Hedges's d of 1.03 ± 0.23 and 0.52 ± 0.09, respectively). Changes in nitrogen availability

  16. Controlling factors of nitrous oxide (N2O) emissions at the field-scale in an agricultural slope

    NASA Astrophysics Data System (ADS)

    Vilain, Guillaume; Garnier, Josette; Tallec, Gaëlle; Tournebize, Julien; Cellier, Pierre; Flipo, Nicolas

    2010-05-01

    Agricultural practices widely contribute to the atmospheric nitrous oxide (N2O) concentration increase and are the major source of N2O which account for 24% of the global annual emission (IPCC, 2007). Soil nitrification and denitrification are the microbial processes responsible for the production of N2O, which also depends on soil characteristics and management. Besides their control by various factors, such as climate, soil conditions and management (content of NO3- and NH4+, soil water content, presence of degradable organic material…), the role of topography is less known although it can play an important role on N2O emissions (Izaurralde et al., 2004). Due to the scarcity of data on N2O direct vs. indirect emission rate from agriculture in the Seine Basin (Garnier et al., 2009), one of the objectives of the study conducted here was to determine the N2O emission rates of the various land use representative for the Seine Basin, in order to better assess the direct N2O emissions, and to explore controlling factor such as meteorology, topography, soil properties and crop successions. The main objective of this study was at the same time to characterize N2O fluxes variability along a transect from an agricultural plateau to a river and to analyze the influence of landscape position on these emissions. We conducted this study in the Orgeval catchment (Seine basin, France; between 48°47' and 48°55' N, and 03°00' and 03°55' E) from May 2008 to August 2009 on two agricultural fields cropped with wheat, barley, oats, corn. N2O fluxes were monitored from weekly to bimonthly using static manual chambers placed along the chosen transect in five different landscape positions from the plateau to the River. This study has shown that soil moisture (expressed as Water Filled Pore Space) and NO3- soil concentrations explained most of the N2O flux variability during the sampling period. Most of N2O was emitted directly after N fertilization application during a relatively

  17. Optimizing rice plant photosynthate allocation reduces N2O emissions from paddy fields

    NASA Astrophysics Data System (ADS)

    Jiang, Yu; Huang, Xiaomin; Zhang, Xin; Zhang, Xingyue; Zhang, Yi; Zheng, Chengyan; Deng, Aixing; Zhang, Jun; Wu, Lianhai; Hu, Shuijin; Zhang, Weijian

    2016-07-01

    Rice paddies are a major source of anthropogenic nitrous oxide (N2O) emissions, especially under alternate wetting-drying irrigation and high N input. Increasing photosynthate allocation to the grain in rice (Oryza sativa L.) has been identified as an effective strategy of genetic and agronomic innovation for yield enhancement; however, its impacts on N2O emissions are still unknown. We conducted three independent but complementary experiments (variety, mutant study, and spikelet clipping) to examine the impacts of rice plant photosynthate allocation on paddy N2O emissions. The three experiments showed that N2O fluxes were significantly and negatively correlated with the ratio of grain yield to total aboveground biomass, known as the harvest index (HI) in agronomy (P < 0.01). Biomass accumulation and N uptake after anthesis were significantly and positively correlated with HI (P < 0.05). Reducing photosynthate allocation to the grain by spikelet clipping significantly increased white root biomass and soil dissolved organic C and reduced plant N uptake, resulting in high soil denitrification potential (P < 0.05). Our findings demonstrate that optimizing photosynthate allocation to the grain can reduce paddy N2O emissions through decreasing belowground C input and increasing plant N uptake, suggesting the potential for genetic and agronomic efforts to produce more rice with less N2O emissions.

  18. Soil CO2, CH4 and N2O effluxes and concentrations in soil profiles down to 15.5m depth in eucalypt plantations under contrasted rainfall regimes

    NASA Astrophysics Data System (ADS)

    Germon, A.; Nouvellon, Y.; Christophe, J.; Chapuis-Lardy, L.; Robin, A.; Rosolem, C. A.; Gonçalves, J. L. D. M.; Guerrini, I. A.; Laclau, J. P.

    2017-12-01

    Silvicultural practices in planted forests affect the fluxes of greenhouse gases at the soil surface and the major factors driving greenhouse gas production in forest soils (substrate supply, temperature, water content,…) vary with soil depth. Our study aimed to assess the consequences of drought on the temporal variability of CO2, CH4 and N2O fluxes throughout very deep soil profiles in Eucalyptus grandis plantations 3 months before the harvest then in coppice, the first 18 months after clear-cutting. Two treatments were compared: one with 37% of throughfall excluded by plastic sheets (TE), and one without rainfall exclusion (WE). Measurements of soil CO2 efflux were made every two weeks for 30 months using a closed-path Li8100 system in both treatment. Every two weeks for 21 months, CO2, CH4 and N2O surface effluxes were measured using the closed-chamber method and concentrations in the soil were measured at 7 depths down to 15.5 m in both TE and WE. At most measurement dates, soil CO2 efflux were significantly higher in TE than in WE. Across the two treatments and the measurement dates, CO2 concentrations increased from 4446 ± 2188 ppm at 10 cm deep to 15622 ± 3523 ppm at 15.5 m, CH4 concentrations increased from 0.41 ± 0.17 ppm at 10 cm deep to 0.77 ± 0.24 ppm at 15.5 m and N2O concentrations remained roughly constant and were on average 478 ± 55 ppb between soil surface and 15.5 m deep. CO2 and N2O concentrations were on average 20.7 and 7.6% lower in TE than in WE, respectively, across the sampling depths. However, CH4 concentrations in TE were on average 44.4% higher than in WE, throughout the soil profile. Those results suggest that extended drought periods might reduce the production of CO2 and N2O but increase the accumulation of CH4 in eucalypt plantations established in deep tropical soils. Very deep tropical soils cover huge areas worldwide and improving our understanding of the spatiotemporal dynamics of gas concentrations in deep soil layers

  19. Measurements of Enthalpy of Sublimation of Ne, N2, O2, Ar, CO2, Kr, Xe, and H2O using a Double Paddle Oscillator.

    PubMed

    Shakeel, Hamza; Wei, Haoyan; Pomeroy, Joshua M

    2018-03-01

    We report precise experimental values of the enthalpy of sublimation (Δ H s ) of quenched condensed films of neon (Ne), nitrogen (N 2 ), oxygen (O 2 ), argon (Ar), carbon dioxide (CO 2 ), krypton (Kr), xenon (Xe), and water (H 2 O) vapor using a single consistent measurement platform. The experiments are performed well below the triple point temperature of each gas and fall in the temperature range where existing experimental data is very limited. A 6 cm 2 and 400 µm thick double paddle oscillator (DPO) with high quality factor (Q ≈ 4 × 10 5 at 298K) and high frequency stability (33 parts per billion) is utilized for the measurements. The enthalpies of sublimation are derived by measuring the rate of mass loss during temperature programmed desorption. The mass change is detected due to change in the resonance frequency of the self-tracking oscillator. Our measurements typically remain within 10% of the available literature, theory, and National Institute of Standards and Technology (NIST) Web Thermo Tables ( WTT ) values, but are performed using an internally consistent method across different gases.

  20. Magnetic and magnetostrictive behavior of Dy 3+ doped CoFe 2O 4 single crystals grown by flux method

    NASA Astrophysics Data System (ADS)

    Kambale, Rahul C.; Song, K. M.; Won, C. J.; Lee, K. D.; Hur, N.

    2012-02-01

    We studied the effect of Dy 3+ content on the magnetic properties of cobalt ferrite single crystal. The single crystals of CoFe 1.9Dy 0.1O 4 were grown by the flux method using Na 2B 4O 7.10 H 2O (Borax) as a solvent (flux). The black and shiny single crystals were obtained as a product. The X-ray diffraction analysis at room temperature confirmed the spinel cubic structure with lattice constant a=8.42 Å of the single crystals. The compositional analysis endorses the presence of constituents Co, Fe and Dy elements after sintering at 1300 °C within the final structure. The magnetic hysteresis measurements at various temperatures viz. 10 K, 100 K, 200 K and 300 K reveal the soft ferrimagnetic nature of the single crystal than that of for pure CoFe 2O 4. The observed saturation magnetization ( Ms) and coercivity ( Hc) are found to be lower than that of pure CoFe 2O 4 single crystal. The magnetostriction ( λ) measurement was carried out along the [001] direction. The magnetic measurements lead to conclude that the present single crystals can be used for magneto-optic recording media.

  1. Molecular approaches to understand the regulation of N2O emission from denitrifying bacteria - model strains and soil communities (Invited)

    NASA Astrophysics Data System (ADS)

    Frostegard, A.; Bakken, L. R.

    2010-12-01

    Emissions of N2O from agricultural soils are largely caused by denitrifying bacteria. Field measurements of N2O fluxes show large variations and depend on several environmental factors, and possibly also on the composition of the denitrifying microbial community. The temporal and spatial variation of fluxes are not adequately captured by biogeochemical models, and few options for mitigations have been invented, which underscores the need to understand the mechanisms underlying the emissions of N2O. Analyses of denitrification genes and transcripts extracted from soils are important for describing the system, but may have limited value for prediction of N2O emissions. In contrast, phenotypic analyses are direct measures of the organisms’ responses to changing environmental conditions. Our approach is to combine phenotypic characterizations using high-resolution gas kinetics, with gene transcription analyses to study denitrification regulatory phenotypes (DRP) of bacterial strains or complex microbial communities. The rich data sets obtained provide a basis for refinement of biochemical and physiological research on this key process in the nitrogen cycle. The strength of this combined approach is illustrated by a series of experiments investigating effects of soil pH on denitrification. Soil pH emerges as a master variable determining the microbial community composition as well as its denitrification product ratio (N2O/N2), with higher ratio in acid than in alkaline soil. It is therefore likely that emissions of N2O from agro-ecosystems will increase in large parts of the world where soil pH is decreasing due to intensified management and increased use of chemical fertilizers. Considering its immense implications, surprisingly few attempts have been made to unravel the mechanisms involved in the pH-control of the product stoichiometry of denitrification. We investigated the kinetics of gas transformations (O2, NO, N2O and N2) and transcription of functional genes

  2. Study the Effect of SiO2 Based Flux on Dilution in Submerged Arc Welding

    NASA Astrophysics Data System (ADS)

    kumar, Aditya; Maheshwari, Sachin

    2017-08-01

    This paper highlights the method for prediction of dilution in submerged arc welding (SAW). The most important factors of weld bead geometry are governed by the weld dilution which controls the chemical and mechanical properties. Submerged arc welding process is used generally due to its very easy control of process variables, good penetration, high weld quality, and smooth finish. Machining parameters, with suitable weld quality can be achieved with the different composition of the flux in the weld. In the present study Si02-Al2O3-CaO flux system was used. In SiO2 based flux NiO, MnO, MgO were mixed in various proportions. The paper investigates the relationship between the process parameters like voltage, % of flux constituents and dilution with the help of Taguchi’s method. The experiments were designed according to Taguchi L9 orthogonal array, while varying the voltage at two different levels in addition to alloying elements. Then the optimal results conditions were verified by confirmatory experiments.

  3. On the production of N2O from the reaction of O/1D/with N2.

    NASA Technical Reports Server (NTRS)

    Simonaitis, R.; Lissi, E.; Heicklen, J.

    1972-01-01

    Ozone was photolyzed at 2537 A and at 25 C in the presence of 42-115 torr of O2 and about 880 torr of N2 to test the relative importance of the two reactions O(1D) + N2 + M leading to N2O + M and O(1D) + N2 leading to O(3P) + N2. In this study N2O was not found as a product. Thus from our detectability limit for N2O an upper limit to the efficiency of the first reaction relative to the second of 2.5 times 10 to the -6 power at 1000-torr total pressure was computed.

  4. Quantification of N2O and NO emissions from a small-scale pond-ditch circulation system for rural polluted water treatment.

    PubMed

    Ma, Lin; Tong, Weijun; Chen, Hongguang; Sun, Jian; Wu, Zhenbin; He, Feng

    2018-04-01

    The pond-ditch circulation system (PDCS) is an efficient and economical solution for the restoration of degraded rural water environments. However, little is known about nitrous oxide (N 2 O) and nitric oxide (NO) emissions in the microbial removal process of nitrogen in PDCSs, and their contribution to nitrogen removal. The aim of this study was to quantify N 2 O and NO emissions from the PDCS, evaluate their capacities, and elucidate the key environmental factors controlling them. The results showed that N 2 O and NO fluxes were in the ranges 1.1-2055.1μgNm -2 h -1 and 0.1-6.8μgNm -2 h -1 for the PDCS, respectively. Meanwhile, the N 2 O and NO fluxes from the two ponds in the PDCS were significantly higher than those in the static system. Moreover, the amount of N 2 O and NO emissions in the PDCS accounted for 0.17-4.32% of the total nitrogen (TN) removal. According to the partial least squares (PLS) approach and Pearson's correlation coefficients, nitrate nitrogen in water (W-NO 3 - -N), dissolved oxygen in water (W-DO), dissolved oxygen in sediment (DO), pH in water (W-pH), pH in sediment (pH), total kjeldahl nitrogen (TKN), and soil organic carbon (SOC) significantly affected the N 2 O flux (p<0.05), whereas W-NO 3 - -N, DO, and nitrite nitrogen in sediment (NO 2 - -N) significantly affected the NO emission (p<0.05). Copyright © 2017 Elsevier B.V. All rights reserved.

  5. On the production of N2O from the reaction of O(1 D) with N2

    NASA Technical Reports Server (NTRS)

    Simonaitis, R.; Lissi, E.; Heicklen, J.

    1972-01-01

    Ozone was photolyzed at 2537 A and 25 C in the presence of 42-115 torr of O2 and about 880 torr of N2 to test the relative importance of the two reactions: (1) O(1D) + N2 + M yields N2O + M, and (2) O(1D) + N2 yields O(3P) + N2. N2O was not found as a product. Thus from our detectability limit for N2O (0.3 micron), an upper limit to the efficiency of the first reaction relative to the second of 0.0000025 at 1000 torr total pressure was computed. This corresponds to k1/k2 smaller than 0.8 x 10 to the minus 25 power cu cm/particle.

  6. O2-MAVS: an Instrument for Measuring Oxygen Flux

    DTIC Science & Technology

    2010-06-01

    al. (2007), “ Coral reefs under rapid climate change and ocean acidification ,” Science 318:1737-1742 [20] K.R.N. Anthony, D.I. Kline, S. Dove, and...O. Hoegh-Guldberg (2008), “ Ocean acidification causes bleaching and productivity loss in coral reef builders,” Proc. Nat. Acad. of Sci. 105:doi...deployments were made on shallow, warm-water coral reefs in La Parguera, Puerto Rico. Time series of net production obtained using the boundary

  7. N2O FIELD STUDY

    EPA Science Inventory

    The report gives results of measurements of nitrous oxide (N2O) emissions from coal-fired utility boilers at three electric power generating stations. Six units were tested, two at each site, including sizes ranging from 165 to 700 MW. Several manufacturers and boiler firing type...

  8. Characteristics of urban-ecosystem atmosphere fluxes of CO2, CH4, N2O, and et over Denver, Colorado

    USGS Publications Warehouse

    Anderson, D.E.; Alvarez, C.; Thienelt, T.

    2004-01-01

    The characteristics of urban ecosystems fluxes of carbon dioxide, methane, nitrous oxide, and evapotranspiration (ET) over Denver, Colorado were discussed. These atmospheric fluxes were measured using a methodology that included a combination of eddy covariance sensors at two levels on a tall tower and chamber measurements at 33 locations on the soil surface. There was both strong temporal and spatial heterogeneity of fluxes owing to characteristics of natural and anthropogenic ecosystem components. Although the urban ecosystem was a net carbon dioxide source, tower-based eddy covariance measurements showed it to be a net vegetative sink during the majority of mid-say summer hours.

  9. Partial nitrogen loss in SrTaO2N and LaTiO2N oxynitride perovskites

    NASA Astrophysics Data System (ADS)

    Chen, Daixi; Habu, Daiki; Masubuchi, Yuji; Torii, Shuki; Kamiyama, Takashi; Kikkawa, Shinichi

    2016-04-01

    SrTaO2N heated in a helium atmosphere began to release nitrogen of approximately 30 at% at 950 °C while maintaining the perovskite structure and its color changed from orange to dark green. Then it decomposed above 1200 °C to a black mixture of Sr1.4Ta0.6O2.73, Ta2N, and Sr5Ta4O15. The second decomposition was not clearly observed when SrTaO2N was heated in a nitrogen atmosphere below 1550 °C. After heating at 1500 °C for 3 h under a 0.2 MPa nitrogen atmosphere, the perovskite product became dark green and conductive. Structure refinement results suggested that the product was a mixture of tetragonal and cubic perovskites with a decreased ordering of N3-/O2-. The sintered body was changed to an n-type semiconductor after a partial loss of nitrogen to be reduced from the originally insulating SrTaO2N perovskite lattice. LaTiO2N was confirmed to have a similar cis-configuration of the TiO4N2 octahedron as that of TaO4N2 in SrTaO2N. It also released some of its nitrogen at 800 °C changing its color from brown to black and then decomposed to a mixture of LaTiO3, La2O3, and TiN at 1100 °C. These temperatures are lower than those in SrTaO2N.

  10. Microbial Oxidation of Fe2+ and Pyrite Exposed to Flux of Micromolar H2O2 in Acidic Media

    PubMed Central

    Ma, Yingqun; Lin, Chuxia

    2013-01-01

    At an initial pH of 2, while abiotic oxidation of aqueous Fe2+ was enhanced by a flux of H2O2 at micromolar concentrations, bio-oxidation of aqueous Fe2+ could be impeded due to oxidative stress/damage in Acidithiobacillus ferrooxidans caused by Fenton reaction-derived hydroxyl radical, particularly when the molar ratio of Fe2+ to H2O2 was low. When pyrite cubes were intermittently exposed to fluxes of micromolar H2O2, the reduced Fe2+-Fe3+ conversion rate in the solution (due to reduced microbial activity) weakened the Fe3+-catalyzed oxidation of cubic pyrite and added to relative importance of H2O2-driven oxidation in the corrosion of mineral surfaces for the treatments with high H2O2 doses. This had effects on reducing the build-up of a passivating coating layer on the mineral surfaces. Cell attachment to the mineral surfaces was only observed at the later stage of the experiment after the solutions became less favorable for the growth of planktonic bacteria. PMID:23760258

  11. Microbial Oxidation of Fe2+ and Pyrite Exposed to Flux of Micromolar H2O2 in Acidic Media

    NASA Astrophysics Data System (ADS)

    Ma, Yingqun; Lin, Chuxia

    2013-06-01

    At an initial pH of 2, while abiotic oxidation of aqueous Fe2+ was enhanced by a flux of H2O2 at micromolar concentrations, bio-oxidation of aqueous Fe2+ could be impeded due to oxidative stress/damage in Acidithiobacillus ferrooxidans caused by Fenton reaction-derived hydroxyl radical, particularly when the molar ratio of Fe2+ to H2O2 was low. When pyrite cubes were intermittently exposed to fluxes of micromolar H2O2, the reduced Fe2+-Fe3+ conversion rate in the solution (due to reduced microbial activity) weakened the Fe3+-catalyzed oxidation of cubic pyrite and added to relative importance of H2O2-driven oxidation in the corrosion of mineral surfaces for the treatments with high H2O2 doses. This had effects on reducing the build-up of a passivating coating layer on the mineral surfaces. Cell attachment to the mineral surfaces was only observed at the later stage of the experiment after the solutions became less favorable for the growth of planktonic bacteria.

  12. Emission of N 2O on pulse-rice crop rotation in upland

    NASA Astrophysics Data System (ADS)

    Ramulu, T. S.; Sahoo, S. K.; Mohapatra, R. K.; Chaudhury, G. Roy; Das, S. N.

    The Seasonally Integrated Flux (SIF) of N 2O emission during pulse cultivation in Rabi season (Season-I: December to April) in rain-fed uplands of Orissa, was found to be 17.7 ± 0.07, 18.7 ± 0.16 and 43.3 ± 0.14 gha -1 for horse gram (HG), black gram (BG) and green gram (GG) respectively. During the subsequent Rabi season (Season-II), the SIF of N 2O for BG and GG cultivated in the same fields were 20.9 ± 0.24 and 38.0 ± 0.42 gha -1 respectively. Similarly SIF values during rice cultivation with different cultivars have also been calculated to be in the range -20.05 ± 0.33 to 21.98 ± 0.29. Statistical analysis showed good correlation of N 2O emission with climatic and soil parameters like temperature, nutrient N and organic matter in soil during pulse cultivation. Multivariate analysis was carried out to factorize the results obtained. Using student ' t' test, the N 2O emission was observed to be similar for two consecutive Rabi seasons for pulses like BG and GG.

  13. Dissociative attachment of electrons to N2O

    NASA Technical Reports Server (NTRS)

    Krishnakumar, E.; Srivastava, S. K.

    1990-01-01

    Cross sections for the production of O(-) from N2O by the process of dissociative electron attachment have been measured for electron-impact energies ranging from 0 to 50 eV. Three new O(-) peaks are observed. The present data above 5-eV electron-impact energy differ considerably from the previous measurements.

  14. Verifying the UK N_{2}O emission inventory with tall tower measurements

    NASA Astrophysics Data System (ADS)

    Carnell, Ed; Meneguz, Elena; Skiba, Ute; Misselbrook, Tom; Cardenas, Laura; Arnold, Tim; Manning, Alistair; Dragosits, Ulli

    2016-04-01

    Nitrous oxide (N2O) is a key greenhouse gas (GHG), with a global warming potential ˜300 times greater than that of CO2. N2O is emitted from a variety of sources, predominantly from agriculture. Annual UK emission estimates are reported, to comply with government commitments under the United Nations Framework Convention on Climate Change (UNFCCC). The UK N2O inventory follows internationally agreed protocols and emission estimates are derived by applying emission factors to estimates of (anthropogenic) emission sources. This approach is useful for comparing anthropogenic emissions from different countries, but does not capture regional differences and inter-annual variability associated with environmental factors (such as climate and soils) and agricultural management. In recent years, the UK inventory approach has been refined to include regional information into its emissions estimates (e.g. agricultural management data), in an attempt to reduce uncertainty. This study attempts to assess the difference between current published inventory methodology (default IPCC methodology) and a revised approach, which incorporates the latest thinking, using data from recent work. For 2013, emission estimates made using the revised approach were 30 % lower than those made using default IPCC methodology, due to the use of lower emission factors suggested by recent projects (www.ghgplatform.org.uk, Defra projects: AC0116, AC0213 and MinNO). The 2013 emissions estimates were disaggregated on a monthly basis using agricultural management (e.g. sowing dates), climate data and soil properties. The temporally disaggregated emission maps were used as input to the Met Office atmospheric dispersion model NAME, for comparison with measured N2O concentrations, at three observation stations (Tacolneston, E England; Ridge Hill, W England; Mace Head, W Ireland) in the UK DECC network (Deriving Emissions linked to Climate Change). The Mace Head site, situated on the west coast of Ireland, was

  15. Global and regional emissions estimates for N2O

    NASA Astrophysics Data System (ADS)

    Saikawa, E.; Prinn, R. G.; Dlugokencky, E.; Ishijima, K.; Dutton, G. S.; Hall, B. D.; Langenfelds, R.; Tohjima, Y.; Machida, T.; Manizza, M.; Rigby, M.; O'Doherty, S.; Patra, P. K.; Harth, C. M.; Weiss, R. F.; Krummel, P. B.; van der Schoot, M.; Fraser, P. J.; Steele, L. P.; Aoki, S.; Nakazawa, T.; Elkins, J. W.

    2014-05-01

    We present a comprehensive estimate of nitrous oxide (N2O) emissions using observations and models from 1995 to 2008. High-frequency records of tropospheric N2O are available from measurements at Cape Grim, Tasmania; Cape Matatula, American Samoa; Ragged Point, Barbados; Mace Head, Ireland; and at Trinidad Head, California using the Advanced Global Atmospheric Gases Experiment (AGAGE) instrumentation and calibrations. The Global Monitoring Division of the National Oceanic and Atmospheric Administration/Earth System Research Laboratory (NOAA/ESRL) has also collected discrete air samples in flasks and in situ measurements from remote sites across the globe and analyzed them for a suite of species including N2O. In addition to these major networks, we include in situ and aircraft measurements from the National Institute of Environmental Studies (NIES) and flask measurements from the Tohoku University and Commonwealth Scientific and Industrial Research Organization (CSIRO) networks. All measurements show increasing atmospheric mole fractions of N2O, with a varying growth rate of 0.1-0.7% per year, resulting in a 7.4% increase in the background atmospheric mole fraction between 1979 and 2011. Using existing emission inventories as well as bottom-up process modeling results, we first create globally gridded a priori N2O emissions over the 37 years since 1975. We then use the three-dimensional chemical transport model, Model for Ozone and Related Chemical Tracers version 4 (MOZART v4), and a Bayesian inverse method to estimate global as well as regional annual emissions for five source sectors from 13 regions in the world. This is the first time that all of these measurements from multiple networks have been combined to determine emissions. Our inversion indicates that global and regional N2O emissions have an increasing trend between 1995 and 2008. Despite large uncertainties, a significant increase is seen from the Asian agricultural sector in recent years, most likely

  16. Comparative study of flux pinning, creep and critical currents between YBaCuO crystals with and without Y2BaCuO5 inclusions

    NASA Technical Reports Server (NTRS)

    Murakami, Masato; Gotoh, Satoshi; Fujimoto, Hiroyuki; Koshizuka, Naoki; Tanaka, Shoji

    1991-01-01

    In the Y-Ba-Cu-O system, YBa2Cu3O(x) phase is produced by the following peritectic reaction: Y2BaCuO5 + liquid yields 2YBa2Cu3O(x). Through the control of processing conditions and starting compositions, it becomes possible to fabricate large crystals containing fine Y2BaCuO5(211) inclusions. Such crystals exhibit Jc values exceeding 10000 A/sq cm at 77 K and 1T. Recently, researchers developed a novel process which can control the volume fraction of 211 inclusions. Elimination of 211 inclusions is also possible. In this study, researchers prepared YBaCuO crystals with and without 211 inclusions using the novel process, and compared flux pinning, flux creep and critical currents. Magnetic field dependence of Jc for YBaCuO crystals with and with 211 inclusions is shown. It is clear that fine 211 inclusions can contribute to flux pinning. It was also found that flux creep rate could be reduced by increasing flux pinning force. Critical current density estimates based on the conventional flux pinning theory were in good agreement with experimental results.

  17. Determination of the rate coefficient for the N2/+/ + O reaction in the ionosphere

    NASA Technical Reports Server (NTRS)

    Torr, D. G.; Torr, M. R.; Orsini, N.; Hanson, W. B.; Hoffman, J. H.; Walker, J. C. G.

    1977-01-01

    Using approximately 400 simultaneous measurements of ion and neutral densities and temperatures, and the spectrum of the solar flux measured by the Atmosphere Explorer C satellite, we have determined the rate constant k1 for the reaction between N2(+) and O in the ionosphere for ion temperatures between 600 and 700 K. We find that k1 = 1.1 x 10 to the minus 10th power cu cm per sec, with a standard deviation of + or - 15%. If we use the temperature dependence for this reaction determined in the laboratory then at 300 K we find excellent agreement with the recommended laboratory value.

  18. Crystal structure of aqua-1κO-{μ-2-[(2-hydroxy-ethyl)methylamino]ethanolato-2:1κ(4) O (1),N,O (2):O (1)}[μ-2,2'-(methylimino)diethanolato-1:2κ(4) O,N,O':O]dithiocyanato-1κN,2κN-chromium(III)copper(II).

    PubMed

    Rusanova, Julia A; Semenaka, Valentina V; Dyakonenko, Viktoriya V; Shishkin, Oleg V

    2015-09-01

    The title compound, [CrCu(C5H11NO2)(C5H12NO2)(NCS)2(H2O)] or [Cr(μ-mdea)Cu(μ-Hmdea)(NCS)2H2O], (where mdeaH2 is N-methylethanolamine, C5H13NO2) is formed as a neutral heterometal Cu(II)/Cr(III) complex. The mol-ecular structure of the complex is based on a binuclear {CuCr(μ-O)2} core. The coordination environment of each metal atom involves the N,O,O atoms of the tridentate ligand, one bridging O atom of the ligand and the N atom of the thio-cyanato ligands. The Cu(II) ion adopts a distorted square-pyramidal coordination while the Cr(III) ion has a distorted octa-hedral coordination geometry completed by the aqua ligand. In the crystal, the binuclear complexes are linked via two pairs of O-H⋯O hydrogen bonds to form inversion dimers, which are arranged in columns parallel to the a axis. In the μ-mdea ligand two -CH2 groups and the methyl group were refined as disordered over two sets of sites with equal occupancies. The structure was refined as a two-component twin with a twin scale factor of 0.242 (1).

  19. Measurement of undisturbed di-nitrogen emissions from aquatic ecosystems

    NASA Astrophysics Data System (ADS)

    Qin, Shuping, Clough, Timothy, Lou, Jiafa; Hu, Chunsheng; Oenema, Oene; Wrage-Mönnig, Nicole; Zhang, Yuming

    2016-04-01

    Increased production of reactive nitrogen (Nr) from atmospheric di-nitrogen (N2) during the last century has greatly contributed to increased food production1-4. However, enriching the biosphere with Nr through N fertilizer production, combustion, and biological N2 fixation has also caused a series of negative effects on global ecosystems 5,6, especially aquatic ecosystems7. The main pathway converting Nr back into the atmospheric N2 pool is the last step of the denitrification process, i.e., the reduction of nitrous oxide (N2O) into N2 by micro-organisms7,8. Despite several attempts9,10, there is not yet an accurate, fast and direct method for measuring undisturbed N2 fluxes from denitrification in aquatic sediments at the field scale11-14. Such a method is essential to study the feedback of aquatic ecosystems to Nr inputs1,2,7. Here we show that the measurement of both N2O emission and its isotope signature can be used to infer the undisturbed N2 fluxes from aquatic ecosystems. The microbial reduction of N2O increases the natural abundance of 15N-N2O relative to 14N-N2O (δ15N-N2O). We observed linear relationships between δ15N-N2O and the logarithmic transformed N2O/(N2+N2O) emission ratios. Through independent measurements, we verified that the undisturbed N2 flux from aquatic ecosystems can be inferred from measurements of N2O emissions and the δ15N-N2O signature. Our method allows the determination of field-scale N2 fluxes from undisturbed aquatic ecosystems, and thereby allows model predictions of denitrification rates to be tested. The undisturbed N2 fluxes observed are almost one order of magnitude higher than those estimated by the traditional method, where perturbation of the system occurs, indicating that the ability of aquatic ecosystems to remove Nr may have been severely underestimated.

  20. {μ-2-[(3-Amino-2,2-dimethyl-prop-yl)imino-meth-yl]-6-meth-oxy-phenolato-1:2κ(5)O(1),O(6):N,N',O(1)}{2-[(3-amino-2,2-dimethyl-prop-yl)imino-meth-yl]-6-meth-oxy-phenolato-1κ(3)N,N',O(1)}-μ-azido-1:2κ(2)N:N-azido-2κN-methanol-2κO-dinickel(II).

    PubMed

    Ghaemi, Akbar; Rayati, Saeed; Fayyazi, Kazem; Ng, Seik Weng; Tiekink, Edward R T

    2012-08-01

    Two distinct coordination geometries are found in the binuclear title complex, [Ni(2)(C(13)H(19)N(2)O(2))(2)(N(3))(2)(CH(3)OH)], as one Schiff base ligand is penta-dentate, coordinating via the anti-cipated oxide O, imine N and amine N atoms (as for the second, tridentate, ligand) but the oxide O is bridging and coordination also occurs through the meth-oxy O atom. The Ni(II) atoms are linked by a μ(2)-oxide atom and one end of a μ(2)-azide ligand, forming an Ni(2)ON core. The coordination geometry for the Ni(II) atom coordinated by the tridentate ligand is completed by the meth-oxy O atom derived from the penta-dentate ligand, with the resulting N(3)O(3) donor set defining a fac octa-hedron. The second Ni(II) atom has its cis-octa-hedral N(4)O(2) coordination geometry completed by the imine N and amine N atoms of the penta-dentate Schiff base ligand, a terminally coordinated azide N and a methanol O atom. The arrangement is stabilized by an intra-molecular hydrogen bond between the methanol H and the oxide O atom. Linear supra-molecular chains along the a axis are formed in the crystal packing whereby two amine H atoms from different amine atoms hydrogen bond to the terminal N atom of the monodentate azide ligand.

  1. Measurement of the photoneutron flux density distribution from cylindrical targets

    NASA Astrophysics Data System (ADS)

    Golovkov, V. M.; Basina, T. N.; Yakovlev, M. R.

    1989-09-01

    Measurements are performed of the density of photoneutron fluxes from cylindrical targets of2H2O (diameter 64 and height 86 mm), Be (outer diameter 70, inner diameter 40, height 100mm), and238U (diameter 44.5 mm, height 50 mm) under the action of braking radiation from electrons with energies of 4 to 8 MeV in order to determine the effect of target form and orientation relative to the detector upon the recorded photoneutron level. The fluxes were measured by an “all-wave” neutron detector based on an SNM-11 counter in a paraffin retarder at an angle of 90‡ to the axis of the braking radiation beam for various target orientations relative to the detector. Measurement results are compared to calculations. Photoneutron fluxes from heavy water and beryllium targets of the indicated dimensions were also measured for angles of 90, 135, and 167‡. An isotropic nature was noted in the photoneutron fluxes from both targets.

  2. Infrared spectroscopic and theoretical study of the HC2n+1O+ (n = 2-5) cations

    NASA Astrophysics Data System (ADS)

    Jin, Jiaye; Li, Wei; Liu, Yuhong; Wang, Guanjun; Zhou, Mingfei

    2017-06-01

    The carbon chain cations, HC2n+1O+ (n = 2-5), are produced via pulsed laser vaporization of a graphite target in supersonic expansions containing carbon monoxide and hydrogen. The infrared spectra are measured via mass-selected infrared photodissociation spectroscopy of the CO "tagged" [HC2n+1O.CO]+ cation complexes in the 1600-3500 cm-1 region. The geometries and electronic ground states of these cation complexes are determined by their infrared spectra compared to the predications of theoretical calculations. All of the HC2n+1O+ (n = 2-5) core cations are characterized to be linear carbon chain derivatives terminated by hydrogen and oxygen, which have the closed-shell singlet ground states with polyyne-like carbon chain structures.

  3. Ecological controls on N2O emission in surface litter and near-surface soil of a managed grassland: modelling and measurements

    NASA Astrophysics Data System (ADS)

    Grant, Robert F.; Neftel, Albrecht; Calanca, Pierluigi

    2016-06-01

    Large variability in N2O emissions from managed grasslands may occur because most emissions originate in surface litter or near-surface soil where variability in soil water content (θ) and temperature (Ts) is greatest. To determine whether temporal variability in θ and Ts of surface litter and near-surface soil could explain this in N2O emissions, a simulation experiment was conducted with ecosys, a comprehensive mathematical model of terrestrial ecosystems in which processes governing N2O emissions were represented at high temporal and spatial resolution. Model performance was verified by comparing N2O emissions, CO2 and energy exchange, and θ and Ts modelled by ecosys with those measured by automated chambers, eddy covariance (EC) and soil sensors on an hourly timescale during several emission events from 2004 to 2009 in an intensively managed pasture at Oensingen, Switzerland. Both modelled and measured events were induced by precipitation following harvesting and subsequent fertilizing or manuring. These events were brief (2-5 days) with maximum N2O effluxes that varied from < 1 mgNm-2h-1 in early spring and autumn to > 3 mgNm-2h-1 in summer. Only very small emissions were modelled or measured outside these events. In the model, emissions were generated almost entirely in surface litter or near-surface (0-2 cm) soil, at rates driven by N availability with fertilization vs. N uptake with grassland regrowth and by O2 supply controlled by litter and soil wetting relative to O2 demand from microbial respiration. In the model, NOx availability relative to O2 limitation governed both the reduction of more oxidized electron acceptors to N2O and the reduction of N2O to N2, so that the magnitude of N2O

  4. The truth is out there: measured, calculated and modelled benthic fluxes.

    NASA Astrophysics Data System (ADS)

    Pakhomova, Svetlana; Protsenko, Elizaveta

    2016-04-01

    In a modern Earth science there is a great importance of understanding the processes, forming the benthic fluxes as one of element sources or sinks to or from the water body, which affects the elements balance in the water system. There are several ways to assess benthic fluxes and here we try to compare the results obtained by chamber experiments, calculated from porewater distributions and simulated with model. Benthic fluxes of dissolved elements (oxygen, nitrogen species, phosphate, silicate, alkalinity, iron and manganese species) were studied in the Baltic and Black Seas from 2000 to 2005. Fluxes were measured in situ using chamber incubations (Jch) and at the same time sediment cores were collected to assess the porewater distribution at different depths to calculate diffusive fluxes (Jpw). Model study was carried out with benthic-pelagic biogeochemical model BROM (O-N-P-Si-C-S-Mn-Fe redox model). It was applied to simulate biogeochemical structure of the water column and upper sediment and to assess the vertical fluxes (Jmd). By the behaviour at the water-sediment interface all studied elements can be divided into three groups: (1) elements which benthic fluxes are determined by the concentrations gradient only (Si, Mn), (2) elements which fluxes depend on redox conditions in the bottom water (Fe, PO4, NH4), and (3) elements which fluxes are strongly connected with organic matter fate (O2, Alk, NH4). For the first group it was found that measured fluxes are always higher than calculated diffusive fluxes (1.5flux. In this case bioturbation, bioirrigation and advection should be taken into account. For the second group measured fluxes can be both much lower (practically absent) and much higher than calculated diffusive fluxes (0.01

  5. Thermophysical Property Measurements of Molten Slag and Welding Flux by Aerodynamic Levitator

    NASA Astrophysics Data System (ADS)

    Onodera, Kenta; Nakamura, Airi; Hakamada, Shinya; Watanabe, Masahito; Kargl, Florian

    Molten slag and welding flux are important materials for steel processing. Due to lack of durable refractory materials, there is limited publication data on the thermophysical properties of these slags. Therefore, in this study, we measured density and viscosity of CaO-Al2O3-SiO2 slag and welding flux using Aerodynamic Levitation (ADL) with CO2-laser heating in which can be achieve containerless and non-contacting conditions for measurements. For density measurements, in order to obtain correct shape of the droplet we used high-speed camera with the extended He-Ne laser to project the shadow image without the influence of the selfluminescence at the high temperature. For viscosity measurement, we also have a unique vibration method; it caused oscillation in a sample by letting gas for levitation vibrate by an acoustic speaker. Using these techniques, we succeeded to measure systematically density and viscosity of molten oxides system.

  6. Detection mechanism and characteristics of ZnO-based N2O sensors operating with photons

    NASA Astrophysics Data System (ADS)

    Jeong, T. S.; Yu, J. H.; Mo, H. S.; Kim, T. S.; Youn, C. J.; Hong, K. J.

    2013-11-01

    N2O sensors made with ZnO-based ZnCdO films were grown on Pyrex substrates by using the RF co-sputtering method. The structure of the N2O sensor was electrode/sensor/glass/illuminant. The mechanism of the photo-assisted oxidation and reduction process on the surface of the N2O sensors was investigated using light from a UV lamp and violet light emitting diode (LED). For photon exposure wavelengths of 365 and 405 nm, the sensitivity of the ZnO-based ZnCdO sensors was measured. From these measurements, the values of the sensitivity of the sensors with x = 0, 0.01, and 0.05 were found to be S = 1.44, 1.39, and 1.33 under LED light with a wavelength of 405 nm, respectively. These sensitivities were compared to those of SnO2 and WO3 materials measured at operating temperatures of 300-600 °C. Also, under exposure with UV light, the response times were observed to be 130 to 270 sec. These response times were slightly slower than that for the traditional method of thermal heating. However, they indicate that the described photon exposure method for N2O detection can replace the conventional heating mode. Consequently, we demonstrated that portable N2O sensors for room-temperature operation could be fabricated without thermal heating.

  7. The O{sub 2} A-Band in the Fluxes and Polarization of Starlight Reflected by Earth-Like Exoplanets

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    Fauchez, Thomas; Rossi, Loic; Stam, Daphne M.

    Earth-like, potentially habitable exoplanets are prime targets in the search for extraterrestrial life. Information about their atmospheres and surfaces can be derived by analyzing the light of the parent star reflected by the planet. We investigate the influence of the surface albedo A {sub s}, the optical thickness b {sub cloud}, the altitude of water clouds, and the mixing ratio of biosignature O{sub 2} on the strength of the O{sub 2} A-band (around 760 nm) in the flux and polarization spectra of starlight reflected by Earth-like exoplanets. Our computations for horizontally homogeneous planets show that small mixing ratios ( ηmore » < 0.4) will yield moderately deep bands in flux and moderate-to-small band strengths in polarization, and that clouds will usually decrease the band depth in flux and the band strength in polarization. However, cloud influence will be strongly dependent on properties such as optical thickness, top altitude, particle phase, coverage fraction, and horizontal distribution. Depending on the surface albedo and cloud properties, different O{sub 2} mixing ratios η can give similar absorption-band depths in flux and band strengths in polarization, especially if the clouds have moderate-to-high optical thicknesses. Measuring both the flux and the polarization is essential to reduce the degeneracies, although it will not solve them, especially not for horizontally inhomogeneous planets. Observations at a wide range of phase angles and with a high temporal resolution could help to derive cloud properties and, once those are known, the mixing ratio of O{sub 2} or any other absorbing gas.« less

  8. A comparison of CH4, N2O and CO2 emissions from three different cover types in a municipal solid waste landfill.

    PubMed

    Wang, Xiaojun; Jia, Mingsheng; Lin, Xiangyu; Xu, Ying; Ye, Xin; Kao, Chih Ming; Chen, Shaohua

    2017-04-01

    High-density polyethylene (HDPE) membranes are commonly used as a cover component in sanitary landfills, although only limited evaluations of its effect on greenhouse gas (GHG) emissions have been completed. In this study, field GHG emission were investigated at the Dongbu landfill, using three different cover systems: HDPE covering; no covering, on the working face; and a novel material-Oreezyme Waste Cover (OWC) material as a trial material. Results showed that the HDPE membrane achieved a high CH 4 retention, 99.8% (CH 4 mean flux of 12 mg C m -2 h -1 ) compared with the air-permeable OWC surface (CH4 mean flux of 5933 mg C m -2 h -1 ) of the same landfill age. Fresh waste at the working face emitted a large fraction of N 2 O, with average fluxes of 10 mg N m -2 h -2 , while N 2 O emissions were small at both the HDPE and the OWC sections. At the OWC section, CH 4 emissions were elevated under high air temperatures but decreased as landfill age increased. N 2 O emissions from the working face had a significant negative correlation with air temperature, with peak values in winter. A massive presence of CO 2 was observed at both the working face and the OWC sections. Most importantly, the annual GHG emissions were 4.9 Gg yr -1 in CO 2 equivalents for the landfill site, of which the OWC-covered section contributed the most CH 4 (41.9%), while the working face contributed the most N 2 O (97.2%). HDPE membrane is therefore, a recommended cover material for GHG control. Monitoring of GHG emissions at three different cover types in a municipal solid waste landfill during a 1-year period showed that the working face was a hotspot of N 2 O, which should draw attention. High CH 4 fluxes occurred on the permeable surface covering a 1- to 2-year-old landfill. In contrast, the high-density polyethylene (HDPE) membrane achieved high CH 4 retention, and therefore is a recommended cover material for GHG control.

  9. Crystal growth and electrical properties of CuFeO 2 single crystals

    NASA Astrophysics Data System (ADS)

    Dordor, P.; Chaminade, J. P.; Wichainchai, A.; Marquestaut, E.; Doumerc, J. P.; Pouchard, M.; Hagenmuller, P.; Ammar, A.

    1988-07-01

    Delafossite-type CuFeO 2 single crystals have been prepared by a flux method: crystals obtained in a Cu crucible with LiBO 2 as flux are n-type whereas those prepared in a Pt crucible with a Cu 2O flux are p-type. Electrical measurements have revealed that n-type crystals exhibit weak anisotropic conductivities with large activation energies and small mobilities (r.t. values perpendicular and parallel to the c-axis: μ⊥ = 5 × 10 -5 and μ‖ = 10 -7 cm -2 V -1 sec -1). p-type crystals, less anisotropic, are characterized by low activation energies and higher mobilities ( μ⊥ = 34 and μ‖ = 8.9 cm 2 V -1 sec -1). A two -conduction-band model is proposed to account for the difference observed between the energy gap value deduced from photoelectrochemical measurements and the activation energy of the electrical conductivity in the intrinsic domain.

  10. Determining oxide trapped charges in Al2O3 insulating films on recessed AlGaN/GaN heterostructures by gate capacitance transients measurements

    NASA Astrophysics Data System (ADS)

    Fiorenza, Patrick; Greco, Giuseppe; Schilirò, Emanuela; Iucolano, Ferdinando; Lo Nigro, Raffaella; Roccaforte, Fabrizio

    2018-05-01

    This letter presents time-dependent gate-capacitance transient measurements (C–t) to determine the oxide trapped charges (N ot) in Al2O3 films deposited on recessed AlGaN/GaN heterostructures. The C–t transients acquired at different temperatures under strong accumulation allowed to accurately monitor the gradual electron trapping, while hindering the re-emission by fast traps that may affect conventional C–V hysteresis measurements. Using this method, an increase of N ot from 2 to 6 × 1012 cm‑2 was estimated between 25 and 150 °C. The electron trapping is ruled by an Arrhenius dependence with an activation energy of 0.12 eV which was associated to points defects present in the Al2O3 films.

  11. Collision cross sections and transport coefficients of O-, O2 -, O3 - and O4 - negative ions in O2, N2 and dry air for non-thermal plasmas modelling

    NASA Astrophysics Data System (ADS)

    Hennad, Ali; Yousfi, Mohammed

    2018-02-01

    The ions interaction data such as interaction potential parameters, elastic and inelastic collision cross sections and the transport coefficients (reduced mobility and diffusion coefficients) have been determined and analyzed in the case of the main negative oxygen ions (O-, O2 -, O3 - and O4 -) present in low temperature plasma at atmospheric pressure when colliding O2, N2 and dry air. The ion transport has been determined from an optimized Monte Carlo simulation using calculated elastic and experimentally fitted inelastic collision cross sections. The elastic momentum transfer collision cross sections have been calculated from a semi-classical JWKB approximation based on a ( n-4) rigid core interaction potential model. The cross sections sets involving elastic and inelastic processes were then validated using measured reduced mobility data and also diffusion coefficient whenever available in the literature. From the sets of elastic and inelastic collision cross sections thus obtained for the first time for O3-/O2, O2 -/N2, O3 -/N2, and O4 -/N2 systems, the ion transport coefficients were calculated in pure gases and dry air over a wide range of the density reduced electric field E/N.

  12. O2-O2 and O2-N2 collision-induced absorption mechanisms unravelled

    NASA Astrophysics Data System (ADS)

    Karman, Tijs; Koenis, Mark A. J.; Banerjee, Agniva; Parker, David H.; Gordon, Iouli E.; van der Avoird, Ad; van der Zande, Wim J.; Groenenboom, Gerrit C.

    2018-05-01

    Collision-induced absorption is the phenomenon in which interactions between colliding molecules lead to absorption of light, even for transitions that are forbidden for the isolated molecules. Collision-induced absorption contributes to the atmospheric heat balance and is important for the electronic excitations of O2 that are used for remote sensing. Here, we present a theoretical study of five vibronic transitions in O2-O2 and O2-N2, using analytical models and numerical quantum scattering calculations. We unambiguously identify the underlying absorption mechanism, which is shown to depend explicitly on the collision partner—contrary to textbook knowledge. This explains experimentally observed qualitative differences between O2-O2 and O2-N2 collisions in the overall intensity, line shape and vibrational dependence of the absorption spectrum. It is shown that these results can be used to discriminate between conflicting experimental data and even to identify unphysical results, thus impacting future experimental studies and atmospheric applications.

  13. Experimental warming of a mountain tundra increases soil CO2 effluxes and enhances CH4 and N2O uptake at Changbai Mountain, China

    PubMed Central

    Zhou, Yumei; Hagedorn, Frank; Zhou, Chunliang; Jiang, Xiaojie; Wang, Xiuxiu; Li, Mai-He

    2016-01-01

    Climatic warming is expected to particularly alter greenhouse gas (GHG) emissions from soils in cold ecosystems such as tundra. We used 1 m2 open-top chambers (OTCs) during three growing seasons to examine how warming (+0.8–1.2 °C) affects the fluxes of carbon dioxide (CO2), methane (CH4) and nitrous oxide (N2O) from alpine tundra soils. Results showed that OTC warming increased soil CO2 efflux by 141% in the first growing season and by 45% in the second and third growing season. The mean CH4 flux of the three growing seasons was −27.6 and −16.7 μg CH4-C m−2h−1 in the warmed and control treatment, respectively. Fluxes of N2O switched between net uptake and emission. Warming didn’t significantly affect N2O emission during the first and the second growing season, but stimulated N2O uptake in the third growing season. The global warming potential of GHG was clearly dominated by soil CO2 effluxes (>99%) and was increased by the OTC warming. In conclusion, soil temperature is the main controlling factor for soil respiration in this tundra. Climate warming will lead to higher soil CO2 emissions but also to an enhanced CH4 uptake with an overall increase of the global warming potential for tundra. PMID:26880107

  14. Intercomparison of six fast-response sensors for the eddy-covariance flux measurement of nitrous oxide over agricultural grassland

    NASA Astrophysics Data System (ADS)

    Nemitz, Eiko; Famulari, Daniela; Ibrom, Andreas; Vermeulen, Alex; Hensen, Arjan; van den Bulk, Pim; Loubet, Benjamin; Laville, Patricia; Mammarella, Ivan; Haapanala, Sami; Lohila, Annalea; Laurila, Tuomas; Eva, Rabot; Laborde, Marie; Cowan, Nicholas; Anderson, Margaret; Helfter, Carole

    2015-04-01

    Nitrous oxide (N2O) is the third most important greenhouse gas and its terrestrial budget remains poorly constraint, with bottom up and top down estimates of country emissions often disagreeing by more than a factor of two. Whilst the measurements of the biosphere / atmosphere exchange of CO2 with micrometeorological methods is commonplace, emissions of CH4 and N2O are more commonly measured with enclosure techniques due to limitations in fast-response sensors with good signal-to-noise characteristics. Recent years have seen the development of a range of instruments based on optical spectroscopy. This started in the early 1990s with instruments based on lead salt lasers, which had temperamental long-term characteristics. More recent developments in quantum cascade lasers has lead to increasingly stable instruments, initially based on pulsed, later on continuous wave lasers. Within the context of the European FP7 Infrastructure Project InGOS ('Integrated non-CO2 Greenhouse gas Observing System'), we conducted an intercomparison of six fast response sensors for N2O: three more or less identical instruments based on off-axis Integrated Cavity Optical Spectrocopy (ICOS) (Los Gatos Research Inc.) and three instruments based on quantum cascade laser absorption spectrometry (Aerodyne Research Inc.): one older generation pulsed instrument (p-QCL) and two of the latest generation of compact continuous wave instruments (cw-QCL), operating at two different wavelengths. One of the ICOS instruments was operated with an inlet drier. In addition, the campaign was joined by a relaxed eddy-accumulation system linked to a FTIR spectrometer (Ecotech), a gradient system based on a home-built slower QCL (INRA Orleans) and a fast chamber system. Here we present the results of the study and a detailed examination of the various corrections and errors of the different instruments. Overall, with the exception of the older generation QCL, the average fluxes based on the different fast

  15. A Tale of Two Gases: Isotope Effects Associated with the Enzymatic Production of H2 and N2O

    NASA Astrophysics Data System (ADS)

    Yang, H.; Gandhi, H.; Kreuzer, H. W.; Moran, J.; Hill, E. A.; McQuarters, A.; Lehnert, N.; Ostrom, N. E.; Hegg, E. L.

    2014-12-01

    Stable isotopes can provide considerable insight into enzymatic mechanisms and fluxes in various biological processes. In our studies, we used stable isotopes to characterize both enzyme-catalyzed H2 and N2O production. H2 is a potential alternative clean energy source and also a key metabolite in many microbial communities. Biological H2 production is generally catalyzed by hydrogenases, enzymes that combine protons and electrons to produce H2 under anaerobic conditions. In our study, H isotopes and fractionation factors (α) were used to characterize two types of hydrogenases: [FeFe]- and [NiFe]-hydrogenases. Due to differences in the active site, the α associated with H2 production for [FeFe]- and [NiFe]-hydrogenases separated into two distinct clusters (αFeFe > αNiFe). The calculated kinetic isotope effects indicate that hydrogenase-catalyzed H2 production has a preference for light isotopes, consistent with the relative bond strengths of O-H and H-H bonds. Interestingly, the isotope effects associated with H2 consumption and H2-H2O exchange reactions were also characterized, but in this case no specific difference was observed between the different enzymes. N2O is a potent greenhouse gas with a global warming potential 300 times that of CO2, and the concentration of N2O is currently increasing at a rate of ~0.25% per year. Thus far, bacterial and fungal denitrification processes have been identified as two of the major sources of biologically generated N2O. In this study, we measured the δ15N, δ18O, δ15Nα (central N atom in N2O), and δ15Nβ (terminal N atom in N2O) of N2O generated by purified fungal P450 nitric oxide reductase (P450nor) from Histoplasma capsulatum. We observed normal isotope effects for δ18O and δ15Nα, and inverse isotope effects for bulk δ15N (the average of Nα and Nβ) and δ15Nβ. The observed isotope effects have been used in conjunction with DFT calculations to provide important insight into the mechanism of P450nor. Similar

  16. N and O isotope (δ15 Nα , δ15 Nβ , δ18 O, δ17 O) analyses of dissolved NO3- and NO2- by the Cd-azide reduction method and N2 O laser spectrometry.

    PubMed

    Wassenaar, Leonard I; Douence, Cedric; Altabet, Mark A; Aggarwal, Pradeep K

    2018-02-15

    The nitrogen and oxygen (δ 15 N, δ 18 O, δ 17 O) isotopic compositions of NO 3 - and NO 2 - are important tracers of nutrient dynamics in soil, rain, groundwater and oceans. The Cd-azide method was used to convert NO 3 - or NO 2 - to N 2 O for N and triple-O isotopic analyses by N 2 O laser spectrometry. A protocol for laser-based headspace isotope analyses was compared with isotope ratio mass spectrometry. Lasers provide the ability to directly measure 17 O anomalies which can help discern atmospheric N sources. δ 15 N, δ 18 O and δ 17 O values were measured on N/O stable isotopic reference materials (IAEA, USGS) by conversion to N 2 O using the Cd-azide method and headspace N 2 O laser spectrometry. A 15 N tracer test assessed the position-specific routing of N to the α or β positions in the N 2 O molecule. A data processing algorithm was used to correct for isotopic dependencies on N 2 O concentration, cavity pressure and water content. NO 3 - /NO 2 - nitrogen is routed to the 15 N α position of N 2 O in the azide reaction; hence the δ 15 N α value should be used for N 2 O laser spectrometry results. With corrections for cavity pressure, N 2 O concentration and water content, the δ 15 N α AIR , δ 18 O VSMOW and δ 17 O VSMOW values (‰) of international reference materials were +4.8 ± 0.1, +25.9 ± 0.3, +12.7 ± 0.2 (IAEA NO 3 ), -1.7 ± 0.1, -26.8 ± 0.8, -14.4 ± 1.1 (USGS34) and +2.6 ± 0.1, +57.6 ± 1.2, +51.2 ± 2.0 (USGS35), in agreement with their values and with the isotope ratio mass spectrometry results. The 17 O excess for USGS35 was +21.2 ± 9‰, in good agreement with previous results. The Cd-azide method yielded excellent results for routine determination of δ 15 N, δ 18 O and δ 17 O values (and the 17 O excess) of nitrate or nitrite by laser spectrometry. Disadvantages are the toxicity of Cd-azide chemicals and the lack of automated sampling devices for N 2 O laser spectrometers. The 15 N-enriched tracer test revealed potential

  17. Eddy Covariance Fluxes of the NO-O3-NO2 Triad above the Forest Canopy at the ATTO Site in the Amazon Basin

    NASA Astrophysics Data System (ADS)

    Tsokankunku, A.; Wolff, S.; Berger, M.; Zelger, M.; Dlugi, R. J. W.; Andreae, M. O.; Sörgel, M.

    2017-12-01

    Nitrogen monoxide (NO) and nitrogen dioxide (NO2) (denoted together as NOx) determine the abundance of the tropospheric oxidants OH, O3 and NO3 that regulate atmospheric self-cleaning. The three reactive trace gases NO, NO2 and O3 undergo a series of interconnected photochemical reactions and are therefore often referred to as the NO-O3-NO2 triad. Ozone deposition is mainly controlled by stomatal uptake, therefore resulting in oxidative stress for the plants. Similarly, nitrogen dioxide from above or below the canopy is deposited to leaves through stomatal uptake. NO emissions from soils contribute to above canopy O3 formation and accelerate OH recycling. Therefore, quantification of the biosphere-atmosphere exchange fluxes of these species is important for atmospheric chemistry and ecosystem research. The eddy covariance method is state of the art for direct measurements of ecosystem fluxes of trace gases. Eddy covariance measurements of NOx in pristine environments are rare because of lack of availability of instruments with the required precision to resolve concentrations characteristic of these environments with the required high time resolution. The Amazon Tall Tower Observatory (ATTO) is located in a pristine rainforest environment in the Amazon basin about 150 km northeast of the city of Manaus. It is the ideal site for studying the biosphere-atmosphere exchange of the NO-O3-NO2 triad, because of the absence of nearby anthropogenic sources. During an intensive measurement campaign in November 2015 at the ATTO site, measurements of NO, NO2 and O3 were carried out at 42 m above ground level on the 80 m walk-up tower with a fast (5 Hz) and sensitive (< 30 ppt) instrument (CLD790SR2, Eco Physics) for NO and NO2 and with 10 Hz for O3 (Enviscope GmbH). Additionally, a suite of micrometeorological instruments was installed, including a profile of 3-dimensional sonic anemometers and meteorological sensors. Vertical concentration profile measurements of NO, NO2 and O

  18. Nitrous Oxide (N2O) Emissions in Wheat and Canola Crops under Fertigation Management in the Canadian Prairies

    NASA Astrophysics Data System (ADS)

    Chai, L.; Hernandez Ramirez, G.; Dyck, M. F.; Pauly, D.; Kryzanowski, L.; Middleton, A.; Powers, L. A.; Lohstraeter, G.; Werk, D.

    2016-12-01

    Nitrous oxide (N2O) emissions from agricultural soils contribute significantly to the amount of greenhouse gases released to the atmosphere every year. Farming practices, such as fertigation in which nitrogen fertilizer is added to crops through irrigation water, could increase the risk for N2O losses. To assess the effect of N fertigation rates on N2O production, field chambers were used to collect weekly gas samples throughout the 2015 growing season in wheat (Triticum aestivum) and canola (Brassica Napus) plots in southern Alberta, Canada. Synthetic fertilizer was either added at seeding or both added at seeding and through irrigation water at one early crop growth stage. The 6 fertilizer treatments were: 60, 90 and 120 kg N ha-1 added at seeding in early May, and 30, 60 and 90 kg N ha-1 at seeding plus another 30 kg N ha-1 added through fertigation in mid-June. Controls with no fertilizer were also evaluated, and each treatment was replicated 4 times. In the wheat plots at a fertilization rate of 120 kg N ha-1, irrespective of single or split application, a larger N2O flux was produced compared to the control (P = 0.024). Similarly, in canola, a total N addition of 90 kg N ha-1 also led to larger N2O fluxes than the control (P = 0.035). The use of fertigation to split the N application had no effect on the N2O emissions in canola; however, in wheat, there was a statistical difference between emissions from 90 kg N ha-1 added all at seeding versus 90 kg N ha-1 split between seeding (60) and fertigation (30); splitting the fertilizer resulted in a 62% decrease in the overall N2O emissions (324 g vs. 524 g N2O-N ha-1; P = 0.039). No other N rates resulted in statistically different N2O emissions when N application was split. These results suggest that fertigation can reduce N2O emissions, but only at moderate N rates (90 kg ha-1 yr-1); conversely, when lower (60) or higher (120) rates are split, emissions remain unaffected.

  19. Investigating the microbial community responsible for unusually high soil N2O and NOx emissions in the Colorado Desert

    NASA Astrophysics Data System (ADS)

    Eberwein, J. R.; Carey, C.; Aronson, E. L.; Jenerette, D.

    2016-12-01

    Although the importance of soil nitrogenous emissions are well accepted in terms of local and global ecological relevance, there remain considerable knowledge gaps concerning the mechanisms regulating production, particularly in arid systems. This study aimed to connect desert soil trace gas emissions of nitrous oxide (N2O) and nitrogen oxides (NOx) with compositional changes in the microbial community. We quantified real-time soil trace gas emissions at two sites in the Colorado Desert experiencing contrasting anthropogenic nitrogen (N) deposition loads (<5 and 15 kg N ha-1 y-1). Measurements were made through 48 hours following water (to simulate a 2 cm rain event) and N additions (at 30 kg NH4NO3 ha-1). In conjunction with flux measurements, soil samples were collected for 16S rRNA gene sequencing to characterize the soil microbial community. N2O fluxes reached as high as 1200 ng N2O-N m-2 s-1, well above most published emissions, but returned to pre-wetting conditions within 12 hours. NOx emissions reached as high as 350 ng NOx-N m-2 s-1 and remained elevated past 24 hours post-wetting. Results from the 16S analysis indicate distinct differences in the microbial community composition between the high and low N deposition sites, with less than 50% of operational taxonomic units (OTUs) in common between sites. N addition had a significant effect on the soil microbial community at the low deposition site, but not at the high deposition site. Furthermore, significant shifts in the bacterial community occurred after wetting, with only one third of the community remaining constant between time points. These results suggest that gaseous N export, particularly N2O emission, is a greater form of nitrogen loss in this system than is currently assumed. Experimental N additions and anthropogenic N deposition show potential for shifting soil microbial community composition, with implications for soil N emissions. Furthermore, shifts in the microbial community can occur as

  20. Gaseous fluxes from subsurface flow constructed wetlands for wastewater treatment.

    PubMed

    Mander, Ulo; Lõhmus, Krista; Teiter, Sille; Nurk, Kaspar; Mauring, Tõnu; Augustin, Jürgen

    2005-01-01

    We measured nitrous oxide (N2O), dinitrogen (N2), and methane (CH4) fluxes in two constructed wetlands (CW) in Estonia using the closed chamber method and the He-O method in the period from October 2000 to March 2003. Emission rates of N2O-N, N2-N and CH4-C from both CWs varied significantly on a both spatial and temporal scale, ranging from 1 to 2,600, 170 to 130,000, and -1.7 to 87,200 microg m(-2) h(-1) respectively. The average flux of N2O from the microsites in the Kodijärve horizontal subsurface flow (HSSF) CW and Kõo hybrid CW ranged from 27 to 370 and from 72 to 500 microg N2O-N m(-2) h(-1), respectively, whereas the average dinitrogen flux from the microsites in the HSSF CW in Kodijärve was 2-3 magnitudes higher than the N2O flux, ranging from 19,500 to 33,300 microg N2-N m(-2) h(-1). The average methane emissions from the microsites in the Kodijärve HSSF CW and the Kõo hybrid CW ranged from 31 to 12,100 and from 950 to 5,750 microg CH4-C m(-2) h(-1), respectively. The highest emission values for all three gases were observed in the warm period. There was a significant relationship between emission rates and water table depth: CH4 and N2 emission increased and N2O emission decreased when the water table did rise. Although the emission of N2O and CH4 from CWs was found to be relatively high, their global warming potential (GWP) in the time horizon of 100 years is not significant, ranging from 4.5 to 16.3 tonnes of CO2 equivalents per ha per year in Kodijärve and from 12.1 to 17.3 t CO2 equivalents ha(-1) yr(-1) in Kõo.

  1. Biochar and denitrification in soils: when, how much and why does biochar reduce N2O emissions?

    PubMed Central

    Cayuela, Maria Luz; Sánchez-Monedero, Miguel Angel; Roig, Asunción; Hanley, Kelly; Enders, Akio; Lehmann, Johannes

    2013-01-01

    Agricultural soils represent the main source of anthropogenic N2O emissions. Recently, interactions of black carbon with the nitrogen cycle have been recognized and the use of biochar is being investigated as a means to reduce N2O emissions. However, the mechanisms of reduction remain unclear. Here we demonstrate the significant impact of biochar on denitrification, with a consistent decrease in N2O emissions by 10–90% in 14 different agricultural soils. Using the 15N gas-flux method we observed a consistent reduction of the N2O/(N2 + N2O) ratio, which demonstrates that biochar facilitates the last step of denitrification. Biochar acid buffer capacity was identified as an important aspect for mitigation that was not primarily caused by a pH shift in soil. We propose the function of biochar as an “electron shuttle” that facilitates the transfer of electrons to soil denitrifying microorganisms, which together with its liming effect would promote the reduction of N2O to N2. PMID:23615819

  2. K-shell photoabsorption coefficients of O2, CO2, CO, and N2O

    NASA Technical Reports Server (NTRS)

    Barrus, D. M.; Blake, R. L.; Burek, A. J.; Chambers, K. C.; Pregenzer, A. L.

    1979-01-01

    The total photoabsorption coefficient has been measured from 500 to 600 eV around the K edge of oxygen in gases O2, CO2, CO, and N2O by means of a gold continuum source and crystal spectrometer with better than 1-eV resolution. The cross sections are dominated by discrete molecular-orbital transitions below the K-edge energy. A few Rydberg transitions were barely detectable. Broad shape resonances appear at or above the K edge. Additional broad, weak features above the K edge possibly arise from shake up. Quantitative results are given that have about 10% accuracy except on the very strong peaks. All the measured features are discussed in relation to other related measurements and theory.

  3. Long-term measurements of atmospheric trace gases (CO2, CH4, N2O, SF6, CO, H2), O2, and δ13CH4 isotopes at Weybourne Atmospheric Observatory, UK: past, present and future

    NASA Astrophysics Data System (ADS)

    Manning, Andrew C.; Forster, Grant L.; Oram, David E.; Reeves, Claire E.; Pickers, Penelope A.; Barningham, S. Thomas; Sturges, William T.; Bandy, Brian; Nisbet, Euan G.; Lowry, David; Fisher, Rebecca; Fleming, Zoe

    2016-04-01

    The Weybourne Atmospheric Observatory (WAO) is situated on the north Norfolk Coast (52.95°N, 1.13°E) in the United Kingdom and is run by the University of East Anglia (UEA), with support from the UK National Centre for Atmospheric Science (NCAS). In 2016, the WAO became a UK-ICOS (Integrated Carbon Observing System) monitoring station. Since 2008, we have been collecting high-precision long-term in situ measurements of atmospheric carbon dioxide (CO2), oxygen (O2), carbon monoxide (CO) and molecular hydrogen (H2), as well as regular bag sampling for δ13CH4. In early 2013, the measurement of atmospheric methane (CH4) commenced, and nitrous oxide (N2O) and sulphur hexafluoride (SF6) began in 2014. We summarise the CO2, O2, CH4, N2O, SF6, CO, H2 and δ13CH4 measurements made to date and highlight some key features observed (e.g. seasonal cycles, long-term trends, pollution events and deposition events). We summarise how the long-term measurements fit into other broader projects which have helped to support the long term time-series at WAO over the years, and highlight how we contribute to broader global atmospheric observation networks.

  4. Measurement of the reaction 18O(α,n)21Ne

    NASA Astrophysics Data System (ADS)

    Best, A.; Falahat, S.; Görres, J.; Couder, M.; deBoer, R.; Güray, R. T.; Kontos, A.; Kratz, K.-L.; LeBlanc, P. J.; Li, Q.; O'Brien, S.; Özkan, N.; Sonnabend, K.; Talwar, R.; Uberseder, E.; Wiescher, M.

    2013-04-01

    Background: The reaction 18O(α,n)21Ne is a part of the reaction chains leading to the production of 19F and 22Ne during He burning in low-mass and massive AGB stars, respectively. Additionally, it has been observed as a strong background source in the measurement of other (α,n) reactions.Purpose: Previously low-energy 18O(α,n)21Ne cross section data have only been available in a non-peer-reviewed form. An improved measurement of this reaction has been done to both clarify its astrophysical influence as well as to provide background yield data for future (α,n) experiments.Method: The 18O(α,n(0+1)) reaction has been measured with a moderating neutron detector. In addition the (α,n1γ) channel has been measured independently by observation of the characteristic 350.7 keV γ transition in 21Ne. The reaction cross section at energies above Eα=1100 keV was determined by a simultaneous R-matrix fit to both channels. The strengths of the two lowest-energy resonances at Eα=959 keV and Eα=1066 keV were analyzed separately using individual Breit-Wigner fits.Results: The cross section of both reaction channels, 18O(α,n0)21Ne and 18O(α,n1γ)21Ne, was determined from the threshold energies at 851 keV and 1280 keV, respectively, to 2300 keV. A new reaction rate has been deduced for the temperature range of 0.1 GK to 10 GK. A previously reported resonance at Eα=888 keV is explained as background from the contaminant reaction 17O(α,n)20Ne.Conclusions: In general, our reaction rate is slightly lower than the reaction rates in recent compilations. At temperatures below 0.2 GK the present rate is significantly lower because it could be shown that the lowest reported resonance is background from the reaction 17O(α,n)20Ne that has been wrongly assigned to 18O(α,n)21Ne.

  5. Potassium (2,2'-bipyridine-κN,N')bis-(carbonato-κO,O')cobaltate(III) dihydrate.

    PubMed

    Wang, Jian-Fei; Lin, Jian-Li

    2010-09-30

    In the title compound, K[Co(CO(3))(2)(C(10)H(8)N(2))]·2H(2)O, the Co(III) atom is coordinated by two bipyridine N atoms and four O atoms from two bidentate chelating carbonate anions, and thus adopts a distorted octa-hedral N(2)O(4) environment. The [Co(bipy)(CO(3))(2)](-) (bipy is 2,2'-bipyridine) -units are stacked along [100] via π-π stacking inter-actions, with inter-planar distances between the bipyridine rings of 3.36 (4) and 3.44 (6) Å, forming chains. Classical O-H⋯O hydrogen-bonding inter-actions link the chains, forming channels along (100) in which the K(+) ions reside and leading to a three-dimensional supra-molecular architecture.

  6. Long-term nitrous oxide fluxes in annual and perennial agricultural and unmanaged ecosystems in the upper Midwest USA

    DOE PAGES

    Gelfand, Ilya; Shcherbak, Iurii; Millar, Neville; ...

    2016-08-11

    Differences in soil nitrous oxide (N 2O) fluxes among ecosystems are often difficult to evaluate and predict due to high spatial and temporal variabilities and few direct experimental comparisons. For 20 years, we measured N 2O fluxes in 11 ecosystems in southwest Michigan USA: four annual grain crops (corn–soybean–wheat rotations) managed with conventional, no-till, reduced input, or biologically based/organic inputs; three perennial crops (alfalfa, poplar, and conifers); and four unmanaged ecosystems of different successional age including mature forest. Average N 2O emissions were higher from annual grain and N-fixing cropping systems than from nonleguminous perennial cropping systems and were low across unmanaged ecosystems. Among annual cropping systems full-rotation fluxes were indistinguishable from one another but rotation phase mattered. For example, those systems with cover crops and reduced fertilizer N emitted more N 2O during the corn and soybean phases, but during the wheat phase fluxes were ~40% lower. Likewise, no-till did not differ from conventional tillage over the entire rotation but reduced emissions ~20% in the wheat phase and increased emissions 30–80% in the corn and soybean phases. Greenhouse gas intensity for the annual crops (flux per unit yield) was lowest for soybeans produced under conventional management, while for the 11 other crop 9 management combinations intensities were similar to one another. Among the fertilized systems, emissions ranged from 0.30 to 1.33 kg N 2O-N ha -1 yr -1 and were best predicted by IPCC Tier 1 and DEF emission factor approaches. Annual cumulative fluxes from perennial systems were best explained by soil NOmore » $$-\\atop{3}$$ pools (r 2 = 0.72) but not so for annual crops, where management differences overrode simple correlations. Daily soil N 2O emissions were poorly predicted by any measured variables. Overall, long-term measurements reveal lower fluxes in nonlegume perennial vegetation and, for

  7. CO2 and N2O emissions from Lou soils of greenhouse tomato fields under aerated irrigation

    NASA Astrophysics Data System (ADS)

    Hou, Huijing; Chen, Hui; Cai, Huanjie; Yang, Fan; Li, Dan; Wang, Fangtong

    2016-05-01

    The change of O2 content in soil caused by aerated irrigation (AI) must inevitably affect the production and emissions of CO2 and N2O from soils. This paper described in-situ observation of CO2 and N2O emissions from AI soils with static chamber-GC technique, in order to reveal the effects of AI on CO2 and N2O emissions from soils of greenhouse tomato fields in autumn-winter season. CO2 and N2O emissions from AI soils mainly concentrated in the blooming and fruit setting period compared to other periods. AI increased cumulative emissions of CO2 and N2O by 11.8% (p = 0.394) and 10.0% (p = 0.480), respectively, compared to the control. The integrative global warming potential of CO2 and N2O on a 100-year horizon for the AI treatment was 6430.60 kg ha-1, increased by 11.7% compared with that for the control (p = 0.356). Both the emissions of CO2 and N2O from AI soils had the exponential positive correlation with soil water-filled pore space (WFPS). The highest peak of CO2 and N2O fluxes from AI soils was observed at 46.7% and 47.5% WFPS, with WFPS ranging from 43.3% to 51.5% and from 45.6% to 52.3% during the whole growth stage, respectively. In addition, the average yield for the AI treatment (34.52 t ha-1) was significantly greater (17.4%) compared with that of the control (p = 0.018). These results suggest that AI do not significantly increase the integrative greenhouse effect caused by CO2 and N2O from soils of greenhouse tomato fields, but significantly increase the tomato yield. The research results provide certain theoretical foundation and scientific basis for accurately evaluating the farmland ecological effect of AI technique.

  8. Can CO2 Turbulent Flux Be Measured by Lidar? A Preliminary Study

    NASA Technical Reports Server (NTRS)

    Gilbert, Fabien; Koch, Grady; Beyon, Jeffrey Y.; Hilton, Timothy W.; Davis, Kenneth J.; Andrews, Arlyn; Flamant, Pierre H.; Singh, Upendra N.

    2011-01-01

    The vertical profiling ofCO2 turbulent fluxes in the atmospheric boundary layer (ABL) is investigated using a coherent differential absorption lidar (CDIAL) operated nearby a tall tower in Wisconsin during June 2007. A CDIAL can perform simultaneous range-resolved CO2 DIAL and velocity measurements. The lidar eddy covariance technique is presented. The aims of the study are (i) an assessment of performance and current limitation of available CDIAL for CO2 turbulent fluxes and (ii) the derivation of instrument specifications to build a future CDIAL to perform accurate range-resolved CO2 fluxes. Experimental lidar CO2 mixing ratio and vertical velocity profiles are successfully compared with in situ sensors measurements. Time and space integral scales of turbulence in the ABL are addressed that result in limitation for time averaging and range accumulation. A first attempt to infer CO2 fluxes using an eddy covariance technique with currently available 2-mm CDIAL dataset is reported.

  9. Conversion of nitrogen oxides in N2:O2:CO2 and N2:O2:CO2:NO2 mixtures subjected to a dc corona discharge

    NASA Astrophysics Data System (ADS)

    Dors, Mirosław; Mizeraczyk, Jerzy

    1996-10-01

    This paper concerns the influence of a direct current (dc) corona discharge on production and reduction of NO, NO2 and N2O in N2:O2:CO2 and N2:O2:CO2:NO2 mixtures. The corona discharge was generated in a needle-to-plate reactor. The positively polarized electrode consisted of 7 needles. The grounded electrode was a stainless steel plate. The gas flow rate through the reactor was varied from 28 to 110 cm3/s. The time-averaged discharge current ranged from 0 to 6 mA. It was found that in the N2:O2:CO2 mixture the corona discharge produced NO, NO2 and N2O. In the N2:O2:CO2:NO2 mixture the reduction of NO2 was between 6-56%, depending on the concentration of O2, gas flow rate and corona discharge current. The NO2 reduction was accompanied by production of NO and N2O. The results show that efficient reduction of nitrogen oxides by a corona discharge cannot be expected in the mixtures containing N2 and O2 if reducing additives are not employed.

  10. Infrared spectra of seeded hydrogen clusters: (para-H2)N-N2O and (ortho-H2)N-N2O, N = 2-13.

    PubMed

    Tang, Jian; McKellar, A R W

    2005-09-15

    High-resolution infrared spectra of clusters containing para-H2 and/or ortho-H2 and a single nitrous oxide molecule are studied in the 2225-cm(-1) region of the upsilon1 fundamental band of N2O. The clusters are formed in pulsed supersonic jet expansions from a cooled nozzle and probed using a tunable infrared diode laser spectrometer. The simple symmetric rotor-type spectra generally show no resolved K structure, with prominent Q-branch features for ortho-H2 but not para-H2 clusters. The observed vibrational shifts and rotational constants are reported. There is no obvious indication of superfluid effects for para-H2 clusters up to N=13. Sharp transitions due to even larger clusters are observed, but no definite assignments are possible. Mixed (para-H2)N-(ortho-H2)M-N2O cluster line positions can be well predicted by linear interpolation between the corresponding transitions of the pure clusters.

  11. Measurements of 89Y(n,2n)88Y and 89Y(n,3n)87Y, 87mY cross sections for fast neutrons at KIRAMS

    NASA Astrophysics Data System (ADS)

    In, Eun Jin; Bak, Sang-In; Ham, Cheolmin; Kim, Do Yoon; Myung, Hyunjeong; Shim, Chungbo; Shin, Jae Won; Min, Kyung Joo; Zhou, Yujie; Park, Tae-Sun; Hong, Seung-Woo; Bhoraskar, V. N.

    2017-09-01

    A proton cyclotron MC-50 in Korea Institute of Radiological & Medical Science (KIRAMS) is used to carry out neutron activation experiments with Y2O3 targets irradiated with neutron beams of a continuous spectrum produced by proton beams on a thick beryllium target. Neutrons are generated by 9Be (p, n) reaction with an incident proton intensity of 20 μA. The neutron spectra generated by proton beams of 30, 35, and 40 MeV are calculated by GEANT4 simulations. Nb powders are used for neutron flux monitoring by measuring the activities of 92mNb through the reaction 93Nb (n, 2n). By using a subtraction method, the average cross section of 89Y(n,2n) and 89Y(n,3n) reactions at the neutron energies of 29.8 ± 1.8 MeV and 34.8 ± 1.8 MeV are extracted and are found to be close to the existing cross sections from the EXFOR data and the evaluated nuclear data libraries such as TENDL-2015 or EAF-2010.

  12. Magnetic flux relaxation in YBa2Cu3O(7-x) thin film: Thermal or athermal

    NASA Technical Reports Server (NTRS)

    Vitta, Satish; Stan, M. A.; Warner, Joseph D.; Alterovitz, Samuel A.

    1992-01-01

    The magnetic flux relaxation behavior of YBa2Cu3O(7-x) thin film on LaAlO3 for H parallel c was studied in the range of 4.2-40 k and 0.2-1.0 T. Both the normalized flux relaxation rate (S) and the net flux pinning energy (U) increase continuously from 1.3 x 10 exp -2 to 3.0 x 10 exp -2 and from 70-240 meV respectively, as the temperature (T) increases from 10 to 40 K. This behavior is consistent with the thermally activated flux motion model. At low temperatures, however, S is found to decrease much more slowly as compared with kT, in contradiction to the thermal activation model. This behavior is discussed in terms of the athermal quantum tunneling of flux lines. The magnetic field dependence of U, however, is not completely understood.

  13. H2O and CO2 fluxes at the floor of a boreal pine forest

    NASA Astrophysics Data System (ADS)

    Kulmala, Liisa; Launiainen, Samuli; Pumpanen, Jukka; Lankreijer, Harry; Lindroth, Anders; Hari, Pertti; Vesala, Timo

    2008-04-01

    We measured H2O and CO2 fluxes at a boreal forest floor using eddy covariance (EC) and chamber methods. Maximum evapotranspiration measured with EC ranged from 1.5 to 2.0mmol m-2 s-1 while chamber estimates depended substantially on the location and the vegetation inside the chamber. The daytime net CO2 exchange measured with EC (0-2μmol m-2 s-1) was of the same order as measured with the chambers. The nocturnal net CO2 exchange measured with the chambers ranged from 4 to 7μmol m-2 s-1 and with EC from ~4 to ~5μmol m-2 s-1 when turbulent mixing below the canopy was sufficient and the measurements were reliable. We studied gross photosynthesis by measuring the light response curves of the most common forest floor species and found the saturated rates of photosynthesis (Pmax) to range from 0.008 (mosses) to 0.184μmol g-1 s-1 (blueberry). The estimated gross photosynthesis at the study site based on average leaf masses and the light response curves of individual plant species was 2-3μmol m-2 s-1. At the same time, we measured a whole community with another chamber and found maximum gross photosynthesis rates from 4 to 7μmol m-2 s-1.

  14. Reduced Snow Cover Increases Wintertime Nitrous Oxide (N 2O) Emissions from an Agricultural Soil in the Upper U.S. Midwest

    DOE PAGES

    Ruan, Leilei; Robertson, G. Philip

    2016-11-21

    Throughout most of the northern hemisphere, snow cover decreased in almost every winter month from 1967 to 2012. Because snow is an effective insulator, snow cover loss has likely enhanced soil freezing and the frequency of soil freeze–thaw cycles, which can disrupt soil nitrogen dynamics including the production of nitrous oxide (N 2O). Here, we used replicated automated gas flux chambers deployed in an annual cropping system in the upper Midwest US for three winters (December–March, 2011–2013) to examine the effects of snow removal and additions on N 2O fluxes. Diminished snow cover resulted in increased N2O emissions each year;more » over the entire experiment, cumulative emissions in plots with snow removed were 69% higher than in ambient snow control plots and 95% higher than in plots that received additional snow (P < 0.001). Higher emissions coincided with a greater number of freeze–thaw cycles that broke up soil macroaggregates (250–8000 µm) and significantly increased soil inorganic nitrogen pools. We conclude that winters with less snow cover can be expected to accelerate N 2O fluxes from agricultural soils subject to wintertime freezing.« less

  15. A Portable FTIR Analyser for Field Measurements of Trace Gases and their Isotopologues: CO2, CH4, N2O, CO, del13C in CO2 and delD in water vapour

    NASA Astrophysics Data System (ADS)

    Griffith, D. W.; Bryant, G. R.; Deutscher, N. M.; Wilson, S. R.; Kettlewell, G.; Riggenbach, M.

    2007-12-01

    We describe a portable Fourier Transform InfraRed (FTIR) analyser capable of simultaneous high precision analysis of CO2, CH4, N2O and CO in air, as well as δ13C in CO2 and δD in water vapour. The instrument is based on a commercial 1 cm-1 resolution FTIR spectrometer fitted with a mid-IR globar source, 26 m multipass White cell and thermoelectrically-cooled MCT detector operating between 2000 and 7500 cm-1. Air is passed through the cell and analysed in real time without any pre-treatment except for (optional) drying. An inlet selection manifold allows automated sequential analysis of samples from one or more inlet lines, with typical measurement times of 1-10 minutes per sample. The spectrometer, inlet sampling sequence, real-time quantitative spectrum analysis, data logging and display are all under the control of a single program running on a laptop PC, and can be left unattended for continuous measurements over periods of weeks to months. Selected spectral regions of typically 100-200 cm-1 width are analysed by a least squares fitting technique to retrieve concentrations of trace gases, 13CO2 and HDO. Typical precision is better than 0.1% without the need for calibration gases. Accuracy is similar if measurements are referenced to calibration standard gases. δ13C precision is typically around 0.1‰, and for δD it is 1‰. Applications of the analyser include clean and polluted air monitoring, tower-based flux measurements such as flux gradient or integrated horizontal flux measurements, automated soil chambers, and field-based measurements of isotopic fractionation in soil-plant-atmosphere systems. The simultaneous multi-component advantages can be exploited in tracer-type emission measurements, for example of CH4 from livestock using a co-released tracer gas and downwind measurement. We have also developed an open path variant especially suited to tracer release studies and measurements of NH3 emissions from agricultural sources. An illustrative

  16. Life on N2O: deciphering the ecophysiology of N2O respiring bacterial communities in a continuous culture.

    PubMed

    Conthe, Monica; Wittorf, Lea; Kuenen, J Gijs; Kleerebezem, Robbert; van Loosdrecht, Mark C M; Hallin, Sara

    2018-04-01

    Reduction of the greenhouse gas N 2 O to N 2 is a trait among denitrifying and non-denitrifying microorganisms having an N 2 O reductase, encoded by nosZ. The nosZ phylogeny has two major clades, I and II, and physiological differences among organisms within the clades may affect N 2 O emissions from ecosystems. To increase our understanding of the ecophysiology of N 2 O reducers, we determined the thermodynamic growth efficiency of N 2 O reduction and the selection of N 2 O reducers under N 2 O- or acetate-limiting conditions in a continuous culture enriched from a natural community with N 2 O as electron acceptor and acetate as electron donor. The biomass yields were higher during N 2 O limitation, irrespective of dilution rate and community composition. The former was corroborated in a continuous culture of Pseudomonas stutzeri and was potentially due to cytotoxic effects of surplus N 2 O. Denitrifiers were favored over non-denitrifying N 2 O reducers under all conditions and Proteobacteria harboring clade I nosZ dominated. The abundance of nosZ clade II increased when allowing for lower growth rates, but bacteria with nosZ clade I had a higher affinity for N 2 O, as defined by μ max /K s . Thus, the specific growth rate is likely a key factor determining the composition of communities living on N 2 O respiration under growth-limited conditions.

  17. Sources of variation in nitrous oxide flux from Amazonian ecosystems

    NASA Technical Reports Server (NTRS)

    Matson, P. A.; Vitousek, P. M.; Livingston, G. P.; Swanberg, N. A.

    1990-01-01

    Nitrous oxide flux and soil nutrient characteristics were measured in three undisturbed tropical ecosystem types, in cleared and burned areas, and in areas of forest converted to pasture near Manaus, Brazil. Nitrogen mineralization, nitrification, and soil nitrogen pools were high in upland forests on clay soils (terra firme) and low in the sand-type and floodplain (varzea) soils. Nitrous oxide flux followed the same pattern, with an average flux of 1.9 ng/sq cm per hr in terra firme, 0.3 in sand types, and 0.1 in varzea. Flux from recently cleared and burned areas did not differ from terra firme forest, but pastures had significantly elevated fluxes (10.3 ng/sq cm per hr). These data were combined with satellite data-based areal estimates of land cover classes to estimate total N2O-N flux from the intensive study area used by the Amazon Boundary Layer Experiment. Total N2O-N flux from the area was 22.9 kg/h; pastures covered 11 percent of the area but accounted for over 40 percent of the flux.

  18. Measurement of Urban fluxes of CO2 and water

    NASA Astrophysics Data System (ADS)

    Grimmond, S.; Crawford, B.; Offerle, B.; Hom, J.

    2006-05-01

    Measurements of surface-atmosphere fluxes of carbon dioxide (FCO2) and latent heat in urban environments are rare even though cities are a major source of atmospheric CO2 and users of water. In this paper, an overview of urban FCO2 measurements will be presented to illustrate how and where such measurements are being conducted and emerging results to date. Most of these studies have been conducted over short periods of time; few studies have considered annual sources/sinks. More investigations have been conducted, and are planned, in European cities than elsewhere, most commonly in areas of medium density urban development. The most dense urban sites are significant net sources of carbon. However, in areas where there is large amounts of vegetation present, there is a net sink of carbon during the summertime. In the second part of the presentation, more detailed attention will be directed to an ongoing measurement program in Baltimore, MD (part of the Baltimore Ecosystem Study). Eddy covariance instrumentation mounted on a tall-tower at 41.2 m has continuously measured local-scale fluxes of carbon dioxide from a suburban environment since 2001. Several features make this particular study unique: 1) for an urban area, the study site is extensively vegetated, 2) the period of record (2001-2005) is among the longest available for urban FCO2 measurements, 3) both closed-path and open-path infrared gas analyzers are used for observations, and 4) several unique data quality control and gap-filling methods have been developed for use in an urban environment. Additionally, detailed surface datasets and GIS software are used to perform flux source area analysis. Results from Baltimore indicate that FCO2 is very dependent on source area land-cover characteristics, particularly the proportion of vegetated and built surfaces. Over the course of a year, the urban surface is a strong net source of CO2, though there is considerable inter-annual variability depending on

  19. Glacial-Interglacial and Holocene N2O Stable Isotope Changes Constrain Terrestrial N Cycling

    NASA Astrophysics Data System (ADS)

    Schmitt, J.; Spahni, R.; Bock, M.; Seth, B.; Stocker, B. D.; Ri, X.; Schilt, A.; Brook, E.; Otto-Bliesner, B. L.; Liu, Z.; Prentice, I. C.; Fischer, H.; Joos, F.

    2015-12-01

    The land biosphere contributes most to the natural source of the long-lived greenhouse gas nitrous oxide (N2O), with N2O emissions being dependent on the turnover rate of both the terrestrial nitrogen (N) and carbon (C) cycle. The C:N stoichiometry of vegetation and soil organic matter links the cycles intimately. Sustained plant productivity increase must be supported by biological N fixation. Intensified N cycling in turn enhances N loss and thereby N2O emissions. The temporal and spatial dynamics of terrestrial N and C cycles and related terrestrial N2O emissions are poorly constrained over the glacial-interglacial transition and the Holocene. Here we reconstruct increased terrestrial N2O emissions since the Last Glacial Maximum based on N2O concentration and isotope measurements on several ice cores and show that this N2O increase can be explained by N cycle modelling - provided N fixation is allowed to respond dynamically to increasing N demand and turnover. The Ice core reconstructions suggest a deglacial increase of 1.1 ± 0.4 Tg N/yr in terrestrial and 0.6 ± 0.4 Tg/yr in oceanic N2O emissions, but relatively constant terrestrial emissions over the Holocene. Transient simulations with a Dynamic Global Vegetation Model are shown to represent the climate and CO2 induced changes in terrestrial N2O emission, and suggest a deglacial increase in biological N fixation by 20%, independently of its absolute magnitude. Deciphering the response of biological N fixation during climatic changes is an important factor for our understanding of plant growth and the land carbon sink, alongside anthropogenic greenhouse gas emissions.

  20. Diode laser-based cavity ring-down instrument for NO3, N2O5, NO, NO2 and O3 from aircraft

    NASA Astrophysics Data System (ADS)

    Wagner, N. L.; Dubé, W. P.; Washenfelder, R. A.; Young, C. J.; Pollack, I. B.; Ryerson, T. B.; Brown, S. S.

    2011-03-01

    This article presents a diode laser based, cavity ring-down spectrometer for simultaneous in situ measurements of four nitrogen oxide species, NO3, N2O5, NO, NO2, as well as O3, designed for deployment on aircraft. The instrument measures NO3 and NO2 by optical extinction at 662 nm and 405 nm, respectively; N2O5 is measured by thermal conversion to NO3, while NO and O3 are measured by chemical conversion to NO2. The instrument has several advantages over previous instruments developed by our group for measurement of NO2, NO3 and N2O5 alone, based on a pulsed Nd:YAG and dye laser. First, the use of continuous wave diode lasers reduces the requirements for power and weight and eliminates hazardous materials. Second, detection of NO2 at 405 nm is more sensitive than our previously reported 532 nm instrument, and does not have a measurable interference from O3. Third, the instrument includes chemical conversion of NO and O3 to NO2 to provide measurements of total NOx (= NO + NO2) and Ox (= NO2 + O3) on two separate channels; mixing ratios of NO and O3 are determined by subtraction of NO2. Finally, all five species are calibrated against a single standard based on 254 nm O3 absorption to provide high accuracy. Disadvantages include an increased sensitivity to water vapor on the 662 nm NO3 and N2O5 channels and a modest reduction in sensitivity for these species compared to the pulsed laser instrument. The measurement precision for both NO3 and N2O5 is below 1 pptv (2σ, 1 s) and for NO, NO2 and O3 is 170, 46, and 56 pptv (2σ, 1 s) respectively. The NO and NO2 measurements are less precise than research-grade chemiluminescence instruments. However, the combination of these five species in a single instrument, calibrated to a single analytical standard, provides a complete and accurate picture of nighttime nitrogen oxide chemistry. The instrument performance is demonstrated using data acquired during a recent field campaign in California.

  1. Measurements of stratospheric NO, NO2, and N2O5 by ISAMS: Preliminary observations and data validation

    NASA Technical Reports Server (NTRS)

    Kerridge, Brian J.; Ballard, J.; Knight, R. J.; Stevens, A. D.; Reburn, J.; Morris, P.; Remedios, John J.; Taylor, Fredric W.

    1994-01-01

    The Improved Stratospheric and Mesospheric Sounder (ISAMS) is a multichannel radiometer and forms part of the science payload of the Upper Atmosphere Research Satellite (UARS). ISAMS measures infrared emissions from the Earth's atmosphere in several wavelength bands. Three such bands include emission from nitric oxide, nitrogen dioxide, and dinitrogen pentoxide. In this paper, we briefly discuss how the ISAMS instrument measures NO, NO2, and N2O5. We also present preliminary data from these channels and describe preliminary validation work.

  2. O2(b1Σg+) Quenching by O2, CO2, H2O, and N2 at Temperatures of 300-800 K.

    PubMed

    Zagidullin, M V; Khvatov, N A; Medvedkov, I A; Tolstov, G I; Mebel, A M; Heaven, M C; Azyazov, V N

    2017-10-05

    Rate constants for the removal of O 2 (b 1 Σ g + ) by collisions with O 2 , N 2 , CO 2 , and H 2 O have been determined over the temperature range from 297 to 800 K. O 2 (b 1 Σ g + ) was excited by pulses from a tunable dye laser, and the deactivation kinetics were followed by observing the temporal behavior of the b 1 Σ g + -X 3 Σ g - fluorescence. The removal rate constants for CO 2 , N 2 , and H 2 O were not strongly dependent on temperature and could be represented by the expressions k CO2 = (1.18 ± 0.05) × 10 -17 × T 1.5 × exp[Formula: see text], k N2 = (8 ± 0.3) × 10 -20 × T 1.5 × exp[Formula: see text], and k H2O = (1.27 ± 0.08) × 10 -16 × T 1.5 × exp[Formula: see text] cm 3 molecule -1 s -1 . Rate constants for O 2 (b 1 Σ g + ) removal by O 2 (X), being orders of magnitude lower, demonstrated a sharp increase with temperature, represented by the fitted expression k O2 = (7.4 ± 0.8) × 10 -17 × T 0.5 × exp[Formula: see text] cm 3 molecule -1 s -1 . All of the rate constants measured at room temperature were found to be in good agreement with previously reported values.

  3. Octa-akis(4-amino-pyridine)-1κN,2κN-aqua-2κO-μ-carbonato-1:2κO,O':O''-dinickel(II) dichloride penta-hydrate.

    PubMed

    Fun, Hoong-Kun; Sinthiya, A; Jebas, Samuel Robinson; Ravindran Durai Nayagam, B; Alfred Cecil Raj, S

    2008-10-18

    In the title compound, [Ni(2)(CO(3))(C(5)H(6)N(2))(8)(H(2)O)]Cl(2)·5H(2)O, one of the the Ni(II) ions is six-coordinated in a distorted octa-hedral geometry, with the equatorial plane defined by four pyridine N atoms from four amino-pyridine ligands, the axial positions being occupied by one water O and a carbonate O atom. The other Ni(II) ion is also six-coordinated, by four other pyridine N atoms from four other amino-pyridine ligands and two carbonate O atoms to complete a distorted octa-hedral geometry. In the crystal structure, mol-ecules are linked into an infinite three-dimensional network by O-H⋯O, N-H⋯Cl, N-H⋯O, O-H⋯N, C-H⋯O, C-H⋯N and C/N-H⋯π inter-actions involving the pyridine rings.

  4. Infrared spectra and tunneling dynamics of the N2-D2O and OC-D2O complexes in the v2 bend region of D2O.

    PubMed

    Zhu, Yu; Zheng, Rui; Li, Song; Yang, Yu; Duan, Chuanxi

    2013-12-07

    The rovibrational spectra of the N2-D2O and OC-D2O complexes in the v2 bend region of D2O have been measured in a supersonic slit jet expansion using a rapid-scan tunable diode laser spectrometer. Both a-type and b-type transitions were observed for these two complexes. All transitions are doubled, due to the heavy water tunneling within the complexes. Assuming the tunneling splittings are the same in K(a) = 0 and K(a) = 1, the band origins, all three rotational and several distortion constants of each tunneling state were determined for N2-D2O in the ground and excited vibrational states, and for OC-D2O in the excited vibrational state, respectively. The averaged band origin of OC-D2O is blueshifted by 2.241 cm(-1) from that of the v2 band of the D2O monomer, compared with 1.247 cm(-1) for N2-D2O. The tunneling splitting of N2-D2O in the ground state is 0.16359(28) cm(-1), which is about five times that of OC-D2O. The tunneling splittings decrease by about 26% for N2-D2O and 23% for OC-D2O, respectively, upon excitation of the D2O bending vibration, indicating an increase of the tunneling barrier in the excited vibrational state. The tunneling splittings are found to have a strong dependence on intramolecular vibrational excitation as well as a weak dependence on quantum number K(a).

  5. Thermo-Physical Properties of B2O3-Containing Mold Flux for High Carbon Steels in Thin Slab Continuous Casters: Structure, Viscosity, Crystallization, and Wettability

    NASA Astrophysics Data System (ADS)

    Park, Jun-Yong; Kim, Gi Hyun; Kim, Jong Bae; Park, Sewoong; Sohn, Il

    2016-08-01

    The effect of B2O3 on the thermo-physical properties of commercial mold fluxes, including the viscosity, crystallization behavior, and wettability, was investigated. Viscosity was measured using the rotating spindle method, and CCT (continuous cooling transformation) diagrams were obtained to investigate the crystallization behavior at various cooling rates using CLSM (confocal laser scanning microscope). The wettability of the fluxes was determined by measuring the contact angles at 1573 K (1300 °C) using the digital images generated by the sessile drop method and were used to calculate the surface tension, interfacial tension, and work of adhesion for Flux A (existing flux) and B (modified flux). These thermo-physical properties were correlated with the structural analysis obtained using FT-IR (Fourier transform-infrared), Raman and MAS-NMR (magic angle spin-nuclear magnetic resonance) spectroscopy. In addition, DTA (differential thermal analysis) was performed on the samples to measure the liquidus temperatures. Higher B2O3 concentrations resulted in lower liquidus temperatures, consequently decreasing the viscosity, the break temperature, and the crystallization temperature. However, B2O3 addition accelerated crystal growth owing to the higher diffusion kinetics of the cations, which also reduced the size of the liquid/solid co-existing region.

  6. Development of a High Precision and Stability Ambient N2O and CO Analyzer

    NASA Astrophysics Data System (ADS)

    Zhou, Jingang; Hoffnagle, John; Tan, Sze; Dong, Feng; Fleck, Derek; Yiu, John; Huang, Kuan; Leggett, Graham; He, Yonggang

    2016-04-01

    With a global warming potential of nearly 300, N2O is a critically important greenhouse gas, contributing about 5 % of the US total GHG emissions. Agriculture soil management practices are the dominant source of anthropogenic N2O emissions, contributing nearly 75 % of US N2O emissions. In urban areas, vehicle tailpipe emissions and waste water treatment plants are significant sources of N2O. We report here a new mid-infrared laser-based cavity ring-down spectrometer (Picarro G5310) that was recently developed to simultaneously measure sub-ppb ambient concentrations of two key greenhouse gas species, N2O and CO, while measuring H2O as well. It combines a quantum cascade laser with a proprietary 3-mirror optical cavity. The ambient N2O and CO measurement precisions are 0.1ppb (10sec), 0.014ppb (600sec), and 0.006ppb (3000sec); and the measurements could even be averaged down over 3 hours, giving measurement precisions of 0.003ppb. The measurable N2O and CO ranges have been tested up to 2.5ppm. With the high precision and unparalleled stability, G5310 is believed a promising tool for long-term monitoring in atmospheric sciences. The new optical analyzer was set up to monitor N2O and CO (G5310), along with CO2 and CH4(G4301), in ambient air obtained from a 10 meter tower in Santa Clara, California. Evidence of contributions from traffic and a nearby sewage treatment facility were expected in the measurement data.

  7. Reviews and syntheses: Soil N2O and NO emissions from land use and land-use change in the tropics and subtropics: a meta-analysis

    NASA Astrophysics Data System (ADS)

    van Lent, J.; Hergoualc'h, K.; Verchot, L. V.

    2015-12-01

    Deforestation and forest degradation in the tropics may substantially alter soil N-oxide emissions. It is particularly relevant to accurately quantify those changes to properly account for them in a REDD+ climate change mitigation scheme that provides financial incentives to reduce the emissions. With this study we provide updated land use (LU)-based emission rates (104 studies, 392 N2O and 111 NO case studies), we determine the trend and magnitude of flux changes with land-use change (LUC) using a meta-analysis approach (44 studies, 135 N2O and 37 NO cases) and evaluate biophysical drivers of N2O and NO emissions and emission changes for the tropics. The average N2O and NO emissions in intact upland tropical forest amounted to 2.0 ± 0.2 (n = 90) and 1.7 ± 0.5 (n = 36) kg N ha-1 yr-1, respectively. In agricultural soils annual N2O emissions were exponentially related to N fertilization rates and average water-filled pore space (WFPS) whereas in non-agricultural sites a Gaussian response to WFPS fit better with the observed NO and N2O emissions. The sum of soil N2O and NO fluxes and the ratio of N2O to NO increased exponentially and significantly with increasing nitrogen availability (expressed as NO3- / [NO3-+NH4+]) and WFPS, respectively; following the conceptual Hole-In-the-Pipe model. Nitrous and nitric oxide fluxes did not increase significantly overall as a result of LUC (Hedges's d of 0.11 ± 0.11 and 0.16 ± 0.19, respectively), however individual LUC trajectories or practices did. Nitrous oxide fluxes increased significantly after intact upland forest conversion to croplands (Hedges's d = 0.78 ± 0.24) and NO increased significantly following the conversion of low forest cover (secondary forest younger than 30 years, woodlands, shrublands) (Hedges's d of 0.44 ± 0.13). Forest conversion to fertilized systems significantly and highly raised both N2O and NO emission rates (Hedges's d of 1.03 ± 0.23 and 0.52 ± 0.09, respectively). Changes in nitrogen

  8. Effects of variation in background mixing ratios of N2, O2, and Ar on the measurement of δ18O-H2O and δ2H-H2O values by cavity ring-down spectroscopy

    NASA Astrophysics Data System (ADS)

    Johnson, Jennifer E.; Rella, Chris W.

    2017-08-01

    Cavity ring-down spectrometers have generally been designed to operate under conditions in which the background gas has a constant composition. However, there are a number of observational and experimental situations of interest in which the background gas has a variable composition. In this study, we examine the effect of background gas composition on a cavity ring-down spectrometer that measures δ18O-H2O and δ2H-H2O values based on the amplitude of water isotopologue absorption features around 7184 cm-1 (L2120-i, Picarro, Inc.). For background mixtures balanced with N2, the apparent δ18O values deviate from true values by -0.50 ± 0.001 ‰ O2 %-1 and -0.57 ± 0.001 ‰ Ar %-1, and apparent δ2H values deviate from true values by 0.26 ± 0.004 ‰ O2 %-1 and 0.42 ± 0.004 ‰ Ar %-1. The artifacts are the result of broadening, narrowing, and shifting of both the target absorption lines and strong neighboring lines. While the background-induced isotopic artifacts can largely be corrected with simple empirical or semi-mechanistic models, neither type of model is capable of completely correcting the isotopic artifacts to within the inherent instrument precision. The development of strategies for dynamically detecting and accommodating background variation in N2, O2, and/or Ar would facilitate the application of cavity ring-down spectrometers to a new class of observations and experiments.

  9. N2O emissions in tropical rainforest and rubber plantation, the indicator from landuse changing in Xishuangbanna, Southwest China

    NASA Astrophysics Data System (ADS)

    Zhou, W. J.; Zhu, J.; Ji, H. L.; Zhang, Y.; Zhang, J.; Zheng, X.

    2016-12-01

    To understand the effects of landuse on N2O emissions and local climate change in the tropics, we measured N2O fluxes from a primary tropical rainforest (TRF, with treatments of litter removal and control) and a fertilized rubber plantation (RP, with treatments of fertilization (75 kg N ha-1 yr-1) and unfertilization) at Xishuangbanna, southwest China since 2012. The results have shown: 1) Fertilized RP N2O emission is bimodel, one peak after dry season fertilizer, another after rainy season fertilizer. Otherwise, the unfertilized RP and TRF have the similar seasonal dynamic with one peak in the middle of rainy season. 2) due to the fertilizer influence, the poaitive correlation between soil temperature/soil moisture and N2O was more significantly in unfertilized RP than fertilized RP respectively litter input changed the dominated controller of N2O emission in TRF: litter carbon input and soil DOC content for control treatment and, soil temperature and soil NO3- -N for litter removal treatment. 3) lab incubation indicated denitrification and nitrification as the main source for N2O emission in TRF and RP, respectively. 4) The N2O emissions from the fertilized and unfertilized plots in RP were 4.0 and 2.5 kg N ha-1 yr-1, respectively, from control and litter removal plots in TRF were 0.48 and 0.32 kg N ha-1 yr-1,respectively. 5) 100-year carbon dioxide equivalence of N2O from fertilized RP offsets 5.8% and 31.5% of carbon sink of the rubber plantation and local TRF, respectively. Upscaling it to the whole Xishuangbanna, N2O emissions from fertilized RP offset 17.1% of the tropical rainforest's carbon sink. When tropical rainforests are converted to fertilized rubber plantations, the N2O emission seasonal dynamic and mechanisms changed, the global warming effect is enhanced.

  10. N2O emissions in tropical rainforest and rubber plantation, the indicator from landuse changing in Xishuangbanna, Southwest China

    NASA Astrophysics Data System (ADS)

    Zhou, Wenjun; Zhu, Jing; Ji, Hong-li; Zhang, Yi-Ping; Sha, Li-Qing; Gao, Jin-Bo; Zhang, Jun-Hui; Zheng, Xunhua

    2017-04-01

    To understand the effects of landuse on N2O emissions and local climate change in the tropics, we measured N2O fluxes from a primary tropical rainforest (TRF, with treatments of litter removal and control) and a fertilized rubber plantation (RP, with treatments of fertilization (75 kg N ha-1 yr-1) and unfertilization) at Xishuangbanna, southwest China since 2012. The results have shown: 1) Fertilized RP N2O emission is bimodel, one peak after dry season fertilizer, another after rainy season fertilizer. Otherwise, the unfertilized RP and TRF have the similar seasonal dynamic with one peak in the middle of rainy season. 2) due to the fertilizer influence, the poaitive correlation between soil temperature/soil moisture and N2O was more significantly in unfertilized RP than fertilized RP respectively litter input changed the dominated controller of N2O emission in TRF: litter carbon input and soil DOC content for control treatment and, soil temperature and soil NO3- -N for litter removal treatment. 3) lab incubation indicated denitrification and nitrification as the main source for N2O emission in TRF and RP, respectively. 4) The N2O emissions from the fertilized and unfertilized plots in RP were 4.0 and 2.5 kg N ha-1 yr-1, respectively, from control and litter removal plots in TRF were 0.48 and 0.32 kg N ha-1 yr-1,respectively. 5) 100-year carbon dioxide equivalence of N2O from fertilized RP offsets 5.8% and 31.5% of carbon sink of the rubber plantation and local TRF, respectively. Upscaling it to the whole Xishuangbanna, N2O emissions from fertilized RP offset 17.1% of the tropical rainforest's carbon sink. When tropical rainforests are converted to fertilized rubber plantations, the N2O emission seasonal dynamic and mechanisms changed, the global warming effect is enhanced.

  11. A kinetic study of the reactions FeO+ + O, Fe+.N2 + O, Fe+.O2 + O and FeO+ + CO: implications for sporadic E layers in the upper atmosphere.

    PubMed

    Woodcock, K R S; Vondrak, T; Meech, S R; Plane, J M C

    2006-04-21

    These gas-phase reactions were studied by pulsed laser ablation of an iron target to produce Fe(+) in a fast flow tube, with detection of the ions by quadrupole mass spectrometry. Fe(+).N(2) and Fe(+).O(2) were produced by injecting N(2) and O(2), respectively, into the flow tube. FeO(+) was produced from Fe(+) by addition of N(2)O, or by ligand-switching from Fe(+).N(2) following the addition of atomic O. The following rate coefficients were measured: k(FeO(+) + O --> Fe(+) + O(2), 186-294 K) = (3.2 +/- 1.5) x 10(-11); k(Fe(+).N(2) + O --> FeO(+)+ N(2), 294 K) = (4.6 +/- 2.5) x 10(-10); k(Fe(+).O(2) + O --> FeO(+) + O(2), 294 K) = (6.3 +/- 2.7) x 10(-11); and k(FeO(+) + CO --> Fe(+) + CO(2), 294 K) = (1.59 +/- 0.34) x 10(-10) cm(3) molecule(-1) s(-1), where the quoted uncertainties are a combination of the 1sigma standard errors in the kinetic data and the systematic experimental errors. The surprisingly slow reaction between FeO(+) and O is examined using ab initio quantum calculations of the relevant potential energy surfaces. The importance of this reaction for controlling the lifetime of sporadic E layers is then demonstrated using a model of the upper mesosphere and lower thermosphere.

  12. Nitrous oxide fluxes from forest floor, tree stems and canopies of boreal tree species during spring

    NASA Astrophysics Data System (ADS)

    Haikarainen, Iikka; Halmeenmäki, Elisa; Machacova, Katerina; Pihlatie, Mari

    2017-04-01

    Boreal forests are considered as small sources of atmospheric nitrous oxide (N2O) due to microbial N2O production in the soils. Recent evidence shows that trees may play an important role in N2O exchange of forest ecosystems by offering pathways for soil produced N2O to the atmosphere. To confirm magnitude, variability and the origin of the tree mediated N2O emissions more research is needed, especially in boreal forests which have been in a minority in such investigation. We measured forest floor, tree stem and shoot N2O exchange of three boreal tree species at the beginning of the growing season (13.4.-13.6.2015) at SMEAR II station in Hyytiälä, located in Southern Finland (61˚ 51´N, 24˚ 17´E, 181 a.s.l.). The fluxes were measured in silver birch (Betula pendula), downy birch (B. pubescens) and Norway spruce (Picea abies) on two sites with differing soil type and characteristics (paludified and mineral soil), vegetation cover and forest structure. The aim was to study the vertical profile of N2O fluxes at stem level and to observe temporal changes in N2O fluxes over the beginning of the growing season. The N2O exchange was determined using the static chamber technique and gas chromatographic analyses. Scaffold towers were used for measurements at multiple stem heights and at the canopy level. Overall, the N2O fluxes from the forest floor and trees at both sites were very small and close to the detection limit. The measured trees mainly emitted N2O from their stems and shoots, while the forest floor acted as a sink of N2O at the paludified site and as a small source of N2O at the mineral soil site. Stem emissions from all the trees at both sites were on average below 0.5 μg N2O m-2 of stem area h-1, and the shoot emissions varied between 0.2 and 0.5 ng N2O m-2 g-1 dry biomass. When the N2O fluxes were scaled up to the whole forest ecosystem, based on the tree biomass and stand density, the N2O emissions from birch and spruce trees at the paludified site

  13. Nitrogen and phosphorus addition impact soil N2O emission in a secondary tropical forest of South China

    PubMed Central

    Wang, Faming; Li, Jian; Wang, Xiaoli; Zhang, Wei; Zou, Bi; Neher, Deborah A.; Li, Zhian

    2014-01-01

    Nutrient availability greatly regulates ecosystem processes and functions of tropical forests. However, few studies have explored impacts of N addition (aN), P addition (aP) and N×P interaction on tropical forests N2O fluxes. We established an N and P addition experiment in a tropical forest to test whether: (1) N addition would increase N2O emission and nitrification, and (2) P addition would increase N2O emission and N transformations. Nitrogen and P addition had no effect on N mineralization and nitrification. Soil microbial biomass was increased following P addition in wet seasons. aN increased 39% N2O emission as compared to control (43.3 μgN2O-N m−2h−1). aP did not increase N2O emission. Overall, N2O emission was 60% greater for aNP relative to the control, but significant difference was observed only in wet seasons, when N2O emission was 78% greater for aNP relative to the control. Our results suggested that increasing N deposition will enhance soil N2O emission, and there would be N×P interaction on N2O emission in wet seasons. Given elevated N deposition in future, P addition in this tropical soil will stimulate soil microbial activities in wet seasons, which will further enhance soil N2O emission. PMID:25001013

  14. Raman study of HgBa 2Ca n-1 Cu nO 2 n+2+ δ ( n=1,2,3,4 and 5) superconductors

    NASA Astrophysics Data System (ADS)

    Zhou, Xingjiang; Cardona, M.; Chu, C. W.; Lin, Q. M.; Loureiro, S. M.; Marezio, M.

    1996-02-01

    Polarized micro-Raman scattering measurements have been performed on the five members of the HgBa 2Ca n-1 Cu nO 2 n+2+ δ ( n=1,2,3,4 and 5) high- Tc superconductor family using different laser frequencies. Local laser annealing measurements were carried out to investigate the variation of the Raman spectra with the excess oxygen content, δ. A systematic evolution of the spectra, which display mainly peaks near 590, 570, 540 and 470 cm -1, with increasing number of CuO 2 layers has been observed; its origin has been shown to lie in the variation of the interstitial oxygen content. In addition to confirming that the 590 cm -1 mode represents vibration of apical oxygens in the absence of neighboring excess oxygen, the 570 cm -1 mode, which may be composed of some finer structures, has been assigned to the vibration of the apical oxygen modified by the presence of the neighboring excess oxygens. The 540 and 470 cm -1 modes may represent the direct vibration of excess oxygens. The implication of possible different distribution sites of excess oxygens is discussed. All other observed lower-frequency modes are also assigned.

  15. Modelling (18)O2 and (16)O2 unidirectional fluxes in plants. III: fitting of experimental data by a simple model.

    PubMed

    André, Marcel J

    2013-08-01

    Photosynthetic assimilation of CO2 in plants results in the balance between the photochemical energy developed by light in chloroplasts, and the consumption of that energy by the oxygenation processes, mainly the photorespiration in C3 plants. The analysis of classical biological models shows the difficulties to bring to fore the oxygenation rate due to the photorespiration pathway. As for other parameters, the most important key point is the estimation of the electron transport rate (ETR or J), i.e. the flux of biochemical energy, which is shared between the reductive and oxidative cycles of carbon. The only reliable method to quantify the linear electron flux responsible for the production of reductive energy is to directly measure the O2 evolution by (18)O2 labelling and mass spectrometry. The hypothesis that the respective rates of reductive and oxidative cycles of carbon are only determined by the kinetic parameters of Rubisco, the respective concentrations of CO2 and O2 at the Rubisco site and the available electron transport rate, ultimately leads to propose new expressions of biochemical model equations. The modelling of (18)O2 and (16)O2 unidirectional fluxes in plants shows that a simple model can fit the photosynthetic and photorespiration exchanges for a wide range of environmental conditions. Its originality is to express the carboxylation and the oxygenation as a function of external gas concentrations, by the definition of a plant specificity factor Sp that mimics the internal reactions of Rubisco in plants. The difference between the specificity factors of plant (Sp) and of Rubisco (Sr) is directly related to the conductance values to CO2 transfer between the atmosphere and the Rubisco site. This clearly illustrates that the values and the variation of conductance are much more important, in higher C3 plants, than the small variations of the Rubisco specificity factor. The simple model systematically expresses the reciprocal variations of

  16. Verifying the UK agricultural N2O emission inventory with tall tower measurements

    NASA Astrophysics Data System (ADS)

    Carnell, E. J.; Meneguz, E.; Skiba, U. M.; Misselbrook, T. H.; Cardenas, L. M.; Arnold, T.; Manning, A.; Dragosits, U.

    2016-12-01

    Nitrous oxide (N2O) is a key greenhouse gas (GHG), with a global warming potential 300 times greater than that of CO2. N2O is emitted from a variety of sources, predominantly from agriculture. Annual UK emission estimates are reported, to comply with government commitments under the United Nations Framework Convention on Climate Change (UNFCCC). The UK N2O inventory follows internationally agreed protocols and emission estimates are derived by applying emission factors to estimates of (anthropogenic) emission sources. This approach is useful for comparing anthropogenic emissions from different countries, but does not capture regional differences and inter-annual variability associated with environmental factors (such as climate and soils) and agricultural management. In recent years, the UK inventory approach has been refined to include regional information into its emissions estimates, in an attempt to reduce uncertainty. This study attempts to assess the difference between current published inventory methodology (default IPCC methodology) and an alternative approach, which incorporates the latest thinking, using data from recent work. For 2013, emission estimates made using the alternative approach were 30 % lower than those made using default IPCC methodology, due to the use of lower emission factors suggested by recent projects (Defra projects: AC0116, AC0213 and MinNO). The 2013 emissions estimates were disaggregated on a monthly basis using agricultural management (e.g. sowing dates), climate data and soil properties. The temporally disaggregated emission maps were used as input to the Met Office atmospheric dispersion model NAME, for comparison with measured N2O concentrations, at three observation stations (Tacolneston, E. England; Ridge Hill, W. England; Mace Head, W. Ireland) in the UK DECC network (Deriving Emissions linked to Climate Change). The Mace Head site, situated on the west coast of Ireland, was used to establish baseline concentrations. The

  17. Soil nitrogen oxide fluxes from lowland forests converted to smallholder rubber and oil palm plantations in Sumatra, Indonesia

    NASA Astrophysics Data System (ADS)

    Hassler, Evelyn; Corre, Marife D.; Kurniawan, Syahrul; Veldkamp, Edzo

    2017-06-01

    Oil palm (Elaeis guineensis) and rubber (Hevea brasiliensis) plantations cover large areas of former rainforest in Sumatra, Indonesia, supplying the global demand for these crops. Although forest conversion is known to influence soil nitrous oxide (N2O) and nitric oxide (NO) fluxes, measurements from oil palm and rubber plantations are scarce (for N2O) or nonexistent (for NO). Our study aimed to (1) quantify changes in soil-atmosphere fluxes of N oxides with forest conversion to rubber and oil palm plantations and (2) determine their controlling factors. In Jambi, Sumatra, we selected two landscapes that mainly differed in texture but were both on heavily weathered soils: loam and clay Acrisol soils. Within each landscape, we investigated lowland forests, rubber trees interspersed in secondary forest (termed as jungle rubber), both as reference land uses and smallholder rubber and oil palm plantations as converted land uses. In the loam Acrisol landscape, we conducted a follow-on study in a large-scale oil palm plantation (called PTPN VI) for comparison of soil N2O fluxes with smallholder oil palm plantations. Land-use conversion to smallholder plantations had no effect on soil N-oxide fluxes (P = 0. 58 to 0.76) due to the generally low soil N availability in the reference land uses that further decreased with land-use conversion. Soil N2O fluxes from the large-scale oil palm plantation did not differ with those from smallholder plantations (P = 0. 15). Over 1-year measurements, the temporal patterns of soil N-oxide fluxes were influenced by soil mineral N and water contents. Across landscapes, annual soil N2O emissions were controlled by gross nitrification and sand content, which also suggest the influence of soil N and water availability. Soil N2O fluxes (µg N m-2 h-1) were 7 ± 2 to 14 ± 7 (reference land uses), 6 ± 3 to 9 ± 2 (rubber), 12 ± 3 to 12 ± 6 (smallholder oil palm) and 42 ± 24 (large-scale oil palm). Soil NO fluxes (µg N m-2 h-1) were

  18. The structure, stability, and infrared spectrum of B 2N, B 2N +, B 2N -, BO, B 2O and B 2N 2.

    NASA Astrophysics Data System (ADS)

    Martin, J. M. L.; François, J. P.; Gijbels, R.

    1992-05-01

    The structure, infrared spectrum, and heat of formation of B 2N, B 2N -, BO, and B 2O have been studied ab initio. B 2N is very stable; B 2O even more so. B 2N, B 2N -, B 2O, and probably B 2N + have symmetric linear ground-state structures; for B 2O, an asymmetric linear structure lies about 12 kcal/mol above the ground state. B 2N +, B 2N - and B 2O have intense asymmetric stretching frequencies, predicted near 870, 1590 and 1400 cm -1, respectively. Our predicted harmonic frequencies and isotopic shifts for B 2O confirm the recent experimental identification by Andrews and Burkholder. Absorptions at 1889.5 and 1998.5 cm -1 in noble-gas trapped boron nitride vapor belong the BNB and BNBN ( 3Π), respectively; a tentative assignment of 882.5 cm -1 to BNB + is proposed. Total atomization energies Σ De (Σ D0) are computed (accuracy ±2 kcal/mol) as: BO 193.1 (190.4), B 2O 292.5 (288.7), B 2N 225.0 (250.3) kcal/mol. The ionization potential and electron affinity of B 2N are predicted to be 8.62±0.1 and 3.34±0.1 eV. The MP4-level additivity approximations involved in G1 theory results in errors on the order of 1 kcal/mol in the Σ De values.

  19. Pinning in the flux-line-cutting regime of Bi 2Sr 2Ca 1Cu 2O 8 single crystals at high field

    NASA Astrophysics Data System (ADS)

    D'Anna, G.; André, M.-O.; Indenbom, M. V.; Benoit, W.

    1994-09-01

    Using a low-frequency torsion pendulum we show that in a Bi 2Sr 2Ca 1Cu 2O 8 single crystal the irreversibility line Birr( T) is frequency dependent down to 10 -5 Hz in the high-field regime. The activation energy has a logarithmic field dependence, U0( B)= U∗ 1n( B∗/ B). A microscopic model for flux-line-cutting and pancake collision yields quantitative expressions for U0 and for Birr( T)= B∗ exp(- T/T∗), which reproduce the experimental data very well.

  20. In situ measurement of solution concentrations and fluxes of sulfonamides and trimethoprim antibiotics in soils using o-DGT.

    PubMed

    Chen, Chang-Er; Chen, Wei; Ying, Guang-Guo; Jones, Kevin C; Zhang, Hao

    2015-01-01

    Techniques, such as Diffusive Gradients in Thin-films (DGT), which either minimally disturb the soil or perturb it in a controlled way are most likely to provide information relevant to toxicity. Herein, we report the first use of DGT for organics (o-DGT) in soil systems to gain insight into the mobility and lability of four antibiotics-sulfamethoxazole (SMX), sulfamethazine (SMZ), and sulfadimethoxine (SDM), trimethoprim (TMP) in soil. In experiments where the same known amount of antibiotics were spiked into the soil, which was then further modified with NaOH, NaCl or dissolved organic matter, directly measured soil solution concentrations (Csoln) of these antibiotics were in the order: SMX>SMZ≈SDM>TMP. The R values (ratio of concentrations measured by o-DGT and directly in solution) were 0.56, 0.41, 0.40 and 0.28, respectively, indicating that the removal of these antibiotics from the solution can be to some extent resupplied by release from the solid phase. The nonlinearity of the relationship between o-DGT fluxes and the reciprocal of diffusive layer thickness (Δg) also suggested that soil solution concentrations were only partially sustained by the solid phase. The potential fluxes of these antibiotics in this soil were 5.4, 3.6, 2.4, and 1.2 pg/cm(2)/s for SMX, SMZ, SDM, and TMP, respectively. o-DGT is a promising tool for understanding the fate and behaviour of polar organic chemicals in soil, and it potentially provides an in situ approach for assessing their bioavailability. Copyright © 2014 Elsevier B.V. All rights reserved.

  1. N2O production by nitrifier denitrification in the Benguela Upwelling System

    NASA Astrophysics Data System (ADS)

    Frame, C. H.; Hou, L.; Lehmann, M. F.

    2014-12-01

    The Benguela upwelling system off the coast of southwestern Africa is an important zone of marine N2O production whose upwelling rates vary seasonally. Here we present N2O stable isotopic and isotopomeric data collected during a period of high upwelling (September 2013) and low upwelling (January 2014). During both periods, 15N-nitrite and 15N-ammonium tracer inucbation experiments were used to investigate N2O production by ammonia oxidizing microorganisms in the top 150m of the water column. N2O production from 15N-ammonium was not measurable during these incubations. However, we detected N2O production from 15N-nitrite, suggesting that nitrifier denitrification is a source of shallow N2O in this region. Furthermore, decreasing the pH of the incubation water enhanced the amount of N2O produced, suggesting that upwelling of CO2-rich/low-pH deep water may enhance N2O production in this region. Finally, we present our incubation data in the larger context of the N2O and nitrite isotopic and concentration profiles, with an eye toward comparing incubation-based N2O production rates with profile-based estimates.

  2. Inverse modelling estimates of N2O surface emissions and stratospheric losses using a global dataset

    NASA Astrophysics Data System (ADS)

    Thompson, R. L.; Bousquet, P.; Chevallier, F.; Dlugokencky, E. J.; Vermeulen, A. T.; Aalto, T.; Haszpra, L.; Meinhardt, F.; O'Doherty, S.; Moncrieff, J. B.; Popa, M.; Steinbacher, M.; Jordan, A.; Schuck, T. J.; Brenninkmeijer, C. A.; Wofsy, S. C.; Kort, E. A.

    2010-12-01

    Nitrous oxide (N2O) levels have been steadily increasing in the atmosphere over the past few decades at a rate of approximately 0.3% per year. This trend is of major concern as N2O is both a long-lived Greenhouse Gas (GHG) and an Ozone Depleting Substance (ODS), as it is a precursor of NO and NO2, which catalytically destroy ozone in the stratosphere. Recently, N2O emissions have been recognised as the most important ODS emissions and are now of greater importance than emissions of CFC's. The growth in atmospheric N2O is predominantly due to the enhancement of surface emissions by human activities. Most notably, the intensification and proliferation of agriculture since the mid-19th century, which has been accompanied by the increased input of reactive nitrogen to soils and has resulted in significant perturbations to the natural N-cycle and emissions of N2O. There exist two approaches for estimating N2O emissions, the so-called 'bottom-up' and 'top-down' approaches. Top-down approaches, based on the inversion of atmospheric measurements, require an estimate of the loss of N2O via photolysis and oxidation in the stratosphere. Uncertainties in the loss magnitude contribute uncertainties of 15 to 20% to the global annual surface emissions, complicating direct comparisons between bottom-up and top-down estimates. In this study, we present a novel inversion framework for the simultaneous optimization of N2O surface emissions and the magnitude of the loss, which avoids errors in the emissions due to incorrect assumptions about the lifetime of N2O. We use a Bayesian inversion with a variational formulation (based on 4D-Var) in order to handle very large datasets. N2O fluxes are retrieved at 4-weekly resolution over a global domain with a spatial resolution of 3.75° x 2.5° longitude by latitude. The efficacy of the simultaneous optimization of emissions and losses is tested using a global synthetic dataset, which mimics the available atmospheric data. Lastly, using real

  3. Imposing strong constraints on tropical terrestrial CO2 fluxes using passenger aircraft based measurements

    NASA Astrophysics Data System (ADS)

    Niwa, Y.; Machida, T.; Sawa, Y.; Matsueda, H.; Schuck, T. J.; Brenninkmeijer, C. A.; Imasu, R.; Satoh, M.

    2011-12-01

    Better understanding of the global and regional carbon budget is needed to perform a reliable prediction of future climate with an earth system model. However, the reliability of CO2 source/sink estimation by inverse modeling, which is one of the promising methods to estimate regional carbon budget, is limited because of sparse observational data coverage. Very few observational data are available in tropics. Therefore, especially the reconstruction of tropical terrestrial fluxes has considerable uncertainties. In this study, regional CO2 fluxes for 2006-2008 are estimated by inverse modeling using the Comprehensive Observation Network for Trace gases by Airliner (CONTRAIL) in addition to the surface measurement dataset of GLOBALVIEW-CO2. CONTRAIL is a recently established CO2 measurement network using in-situ measurement instruments on board commercial aircraft. Five CONTRAIL aircraft travel back and forth between Japan and many areas: Europe, North America, Southeast Asia, South Asia, and Australia. The Bayesian synthesis approach is used to estimate monthly fluxes for 42 regions using NICAM-TM simulations with existing CO2 flux datasets and monthly mean observational data. It is demonstrated that the aircraft data have great impact on estimated tropical terrestrial fluxes. By adding the aircraft data to the surface data, the analyzed uncertainty of tropical fluxes has been reduced by 15 % and more than 30 % uncertainty reduction rate is found in Southeast and South Asia. Specifically, for annual net CO2 fluxes, nearly neutral fluxes of Indonesia, which is estimated using the surface dataset alone, turn to positive fluxes, i.e. carbon sources. In Indonesia, a remarkable carbon release during the severe drought period of October-December in 2006 is estimated, which suggests that biosphere respiration or biomass burning was larger than the prior fluxes. Comparison of the optimized atmospheric CO2 with independent aircraft measurements of CARIBIC tends to validate

  4. Linking water and carbon fluxes in a Mediterranean oak woodland using a combined flux and ?18O partitioning approach

    NASA Astrophysics Data System (ADS)

    Dubbert, M.; Piayda, A.; Costa e Silva, F.; Correia, A.; Pereira, J. S.; Cuntz, M.; Werner, C.

    2013-12-01

    Water is one of the key factors driving ecosystem productivity, especially in water-limited ecosystems, where global climate change is expected to intensify drought and alter precipitation patterns. One such ecosystem is the ';Montado', where two vegetation layers respond differently to drought: oak trees avoid drought due to their access to deeper soil layers and ground water while herbaceous plants, surviving the summer in the form of seeds. We aimed at 1) quantifying the impact of the understory herbaceous vegetation on ecosystem carbon and water fluxes throughout the year, 2) determining the driving environmental factors for evapotranspiration (ET) and net ecosystem exchange (NEE) and 3) disentangling how ET components of the ecosystem relate to carbon dioxide exchange. We present one year data set comparing modeled and measured stable oxygen isotope signatures (δ18O) of soil evaporation, confirming that the Craig and Gordon equation leads to good agreement with measured δ18O of evaporation (Dubbert et al. 2013). Partitioning ecosystem ET and NEE into its three sources revealed a strong contribution of soil evaporation (E) and herbaceous transpiration (T) to ecosystem ET during spring and fall. In contrast, soil respiration (R) and herbaceous net carbon gain contributed to a lesser amount to ecosystem NEE during spring and fall, leading to consistently smaller water use efficiencies (WUE) of the herbaceous understory compared to the cork-oaks. Here, we demonstrate that the ability to assess ET, NEE and WUE independent of soil evaporation dynamics enables the understanding of the mechanisms of the coupling between water and carbon fluxes and their responses to drought. Dubbert, M., Cuntz, M., Piayda, A., Maguas, C., Werner, C., 2013: Partitioning evapotranspiration - Testing the Craig and Gordon model with field measurements of oxygen isotope ratios of evaporative fluxes. J Hydrol. a) Oxygen isotope signatures of soil evaporation on bare soil plots calculated

  5. Photolysis of H2O-H2O2 Mixtures: The Destruction of H2O2

    NASA Technical Reports Server (NTRS)

    Loeffler, M. J.; Fama, M.; Baragiola, R. A.; Carlson, R. W.

    2013-01-01

    We present laboratory results on the loss of H2O2 in solid H2O + H2O2 mixtures at temperatures between 21 and 145 K initiated by UV photolysis (193 nm). Using infrared spectroscopy and microbalance gravimetry, we measured the decrease of the 3.5 micrometer infrared absorption band during UV irradiation and obtained a photodestruction cross section that varies with temperature, being lowest at 70 K. We use our results, along with our previously measured H2O2 production rates via ionizing radiation and ion energy fluxes from the spacecraft to compare H2O2 creation and destruction at icy satellites by ions from their planetary magnetosphere and from solar UV photons. We conclude that, in many cases, H2O2 is not observed on icy satellite surfaces because the H2O2 photodestruction rate is much higher than the production rate via energetic particles, effectively keeping the H2O2 infrared signature at or below the noise level.

  6. A True Eddy Accumulation - Eddy Covariance hybrid for measurements of turbulent trace gas fluxes

    NASA Astrophysics Data System (ADS)

    Siebicke, Lukas

    2016-04-01

    Eddy covariance (EC) is state-of-the-art in directly and continuously measuring turbulent fluxes of carbon dioxide and water vapor. However, low signal-to-noise ratios, high flow rates and missing or complex gas analyzers limit it's application to few scalars. True eddy accumulation, based on conditional sampling ideas by Desjardins in 1972, requires no fast response analyzers and is therefore potentially applicable to a wider range of scalars. Recently we showed possibly the first successful implementation of True Eddy Accumulation (TEA) measuring net ecosystem exchange of carbon dioxide of a grassland. However, most accumulation systems share the complexity of having to store discrete air samples in physical containers representing entire flux averaging intervals. The current study investigates merging principles of eddy accumulation and eddy covariance, which we here refer to as "true eddy accumulation in transient mode" (TEA-TM). This direct flux method TEA-TM combines true eddy accumulation with continuous sampling. The TEA-TM setup is simpler than discrete accumulation methods while avoiding the need for fast response gas analyzers and high flow rates required for EC. We implemented the proposed TEA-TM method and measured fluxes of carbon dioxide (CO2), methane (CH4) and water vapor (H2O) above a mixed beech forest at the Hainich Fluxnet and ICOS site, Germany, using a G2301 laser spectrometer (Picarro Inc., USA). We further simulated a TEA-TM sampling system using measured high frequency CO2 time series from an open-path gas analyzer. We operated TEA-TM side-by-side with open-, enclosed- and closed-path EC flux systems for CO2, H2O and CH4 (LI-7500, LI-7200, LI-6262, LI-7700, Licor, USA, and FGGA LGR, USA). First results show that TEA-TM CO2 fluxes were similar to EC fluxes. Remaining differences were similar to those between the three eddy covariance setups (open-, enclosed- and closed-path gas analyzers). Measured TEA-TM CO2 fluxes from our physical

  7. Mitigation potential of soil carbon management overestimated by neglecting N2O emissions

    NASA Astrophysics Data System (ADS)

    Lugato, Emanuele; Leip, Adrian; Jones, Arwyn

    2018-03-01

    International initiatives such as the `4 per 1000' are promoting enhanced carbon (C) sequestration in agricultural soils as a way to mitigate greenhouse gas emissions1. However, changes in soil organic C turnover feed back into the nitrogen (N) cycle2, meaning that variation in soil nitrous oxide (N2O) emissions may offset or enhance C sequestration actions3. Here we use a biogeochemistry model on approximately 8,000 soil sampling locations in the European Union4 to quantify the net CO2 equivalent (CO2e) fluxes associated with representative C-mitigating agricultural practices. Practices based on integrated crop residue retention and lower soil disturbance are found to not increase N2O emissions as long as C accumulation continues (until around 2040), thereafter leading to a moderate C sequestration offset mostly below 47% by 2100. The introduction of N-fixing cover crops allowed higher C accumulation over the initial 20 years, but this gain was progressively offset by higher N2O emissions over time. By 2060, around half of the sites became a net source of greenhouse gases. We conclude that significant CO2 mitigation can be achieved in the initial 20-30 years of any C management scheme, but after that N inputs should be controlled through appropriate management.

  8. Diode laser-based cavity ring-down instrument for NO3, N2O5, NO, NO2 and O3 from aircraft

    NASA Astrophysics Data System (ADS)

    Wagner, N. L.; Dubé, W. P.; Washenfelder, R. A.; Young, C. J.; Pollack, I. B.; Ryerson, T. B.; Brown, S. S.

    2011-06-01

    This article presents a diode laser-based, cavity ring-down spectrometer for simultaneous in situ measurements of four nitrogen oxide species, NO3, N2O5, NO, NO2, as well as O3, designed for deployment on aircraft. The instrument measures NO3 and NO2 by optical extinction at 662 nm and 405 nm, respectively; N2O5 is measured by thermal conversion to NO3, while NO and O3 are measured by chemical conversion to NO2. The instrument has several advantages over previous instruments developed by our group for measurement of NO2, NO3 and N2O5 alone, based on a pulsed Nd:YAG and dye laser. First, the use of continuous wave diode lasers reduces the requirements for power and weight and eliminates hazardous materials. Second, detection of NO2 at 405 nm is more sensitive than our previously reported 532 nm instrument, and does not have a measurable interference from O3. Third, the instrument includes chemical conversion of NO and O3 to NO2 to provide measurements of total NOx (= NO + NO2) and Ox (= NO2 + O3) on two separate channels; mixing ratios of NO and O3 are determined by subtraction of NO2. Finally, all five species are calibrated against a single standard based on 254 nm O3 absorption to provide high accuracy. Disadvantages include an increased sensitivity to water vapor on the 662 nm NO3 and N2O5 channels and a modest reduction in sensitivity for these species compared to the pulsed laser instrument. The in-flight detection limit for both NO3 and N2O5 is 3 pptv (2 σ, 1 s) and for NO, NO2 and O3 is 140, 90, and 120 pptv (2 σ, 1 s) respectively. Demonstrated performance of the instrument in a laboratory/ground based environment is better by approximately a factor of 2-3. The NO and NO2 measurements are less precise than research-grade chemiluminescence instruments. However, the combination of these five species in a single instrument, calibrated to a single analytical standard, provides a complete and accurate picture of nighttime nitrogen oxide chemistry. The

  9. Imposing strong constraints on tropical terrestrial CO2 fluxes using passenger aircraft based measurements

    NASA Astrophysics Data System (ADS)

    Niwa, Yosuke; Machida, Toshinobu; Sawa, Yousuke; Matsueda, Hidekazu; Schuck, Tanja J.; Brenninkmeijer, Carl A. M.; Imasu, Ryoichi; Satoh, Masaki

    2012-06-01

    Because very few measurements of atmospheric carbon dioxide (CO2) are available in the tropics, estimates of surface CO2 fluxes in tropical regions are beset with considerable uncertainties. To improve estimates of tropical terrestrial fluxes, atmospheric CO2 inversion was performed using passenger aircraft based measurements of the Comprehensive Observation Network for Trace gases by Airliner (CONTRAIL) project in addition to the surface measurement data set of GLOBALVIEW-CO2. Regional monthly fluxes at the earth's surface were estimated using the Bayesian synthesis approach focusing on the period 2006-2008 using the Nonhydrostatic Icosahedral Atmospheric Model-based Transport Model (NICAM-TM). By adding the aircraft to the surface data, the posterior flux errors were greatly reduced; specifically, error reductions of up to 64% were found for tropical Asia regions. This strong impact is closely related to efficient vertical transport in the tropics. The optimized surface fluxes using the CONTRAIL data were evaluated by comparing the simulated atmospheric CO2 distributions with independent aircraft measurements of the Civil Aircraft for the Regular Investigation of the atmosphere Based on an Instrument Container (CARIBIC) project. The inversion with the CONTRAIL data yields the global carbon sequestration rates of 2.22 ± 0.28 Pg C yr-1 for the terrestrial biosphere and 2.24 ± 0.27 Pg C yr-1 for the oceans (the both are adjusted by riverine input of CO2). For the first time the CONTRAIL CO2 measurements were used in an inversion system to identify the areas of greatest impact in terms of reducing flux uncertainties.

  10. Measurement of 235U(n,n'γ) and 235U(n,2nγ) reaction cross sections

    NASA Astrophysics Data System (ADS)

    Kerveno, M.; Thiry, J. C.; Bacquias, A.; Borcea, C.; Dessagne, P.; Drohé, J. C.; Goriely, S.; Hilaire, S.; Jericha, E.; Karam, H.; Negret, A.; Pavlik, A.; Plompen, A. J. M.; Romain, P.; Rouki, C.; Rudolf, G.; Stanoiu, M.

    2013-02-01

    The design of generation IV nuclear reactors and the studies of new fuel cycles require knowledge of the cross sections of various nuclear reactions. Our research is focused on (n,xnγ) reactions occurring in these new reactors. The aim is to measure unknown cross sections and to reduce the uncertainty on present data for reactions and isotopes of interest for transmutation or advanced reactors. The present work studies the 235U(n,n'γ) and 235U(n,2nγ) reactions in the fast neutron energy domain (up to 20 MeV). The experiments were performed with the Geel electron linear accelerator GELINA, which delivers a pulsed white neutron beam. The time characteristics enable measuring neutron energies with the time-of-flight (TOF) technique. The neutron induced reactions [in this case inelastic scattering and (n,2n) reactions] are identified by on-line prompt γ spectroscopy with an experimental setup including four high-purity germanium (HPGe) detectors. A fission ionization chamber is used to monitor the incident neutron flux. The experimental setup and analysis methods are presented and the model calculations performed with the TALYS-1.2 code are discussed.

  11. Detection of interstellar N2O: A new molecule containing an N-O bond

    NASA Technical Reports Server (NTRS)

    Ziurys, L. M.; Apponi, A. J.; Hollis, J. M.; Snyder, L. E.

    1994-01-01

    A new interstellar molecule, N2O, known as nitrous oxide or 'laughing gas,' has been detected using the NRAO 12 m telescope. The J = 3 - 2, 4 - 3, 5 - 4, and 6 - 5 rotational transitions of this species at 75, 100, 125, and 150 GHz, respectively, were observed toward Sgr B2(M). The column density derived for N2O in this source is N(sub tot) approx. 10(exp 15)/sq. cm, which corresponds to a fractional abundance of approx. 10(exp -9), relative to H2. This value implies abundance ratios of N2O/NO approx. 0.1 and N2O/HNO approx. 3 in the Galactic center. Such ratios are in excellent agreement with predictions of ion-molecule models of interstellar chemistry using early-time calculations and primarily neutral-neutral reactions. N2O is the third interstellar molecule detected thus far containing an N-O bond. Such bonds cannot be so rare as previously thought.

  12. Effect of Compositional Variation in TiO2-Based Flux-Cored Arc Welding Fluxes on the Thermo-physical Properties and Mechanical Behavior of a Weld Zone

    NASA Astrophysics Data System (ADS)

    Kim, J. B.; Lee, T. H.; Sohn, I.

    2018-04-01

    The effect of compositional variation in TiO2-based flux-cored arc welding fluxes on viscosity, wettability, and electronegativity was studied. The thermo-physical properties of the retrieved fluxes and their relationship with the mechanical properties of the weld zone, including tensile strength and micro-Vickers hardness, after welding were identified. Microstructural observation under similar welding conditions revealed significant grain coarsening at a corrected optical basicity (Λcorr) of 0.62, resulting in reduced strength and hardness due to greater heat transfer. Welding fluxes containing TiO2-based simple structural units should result in greater heat transfer due to the deficiency in complex [AlO4]5-- and [SiO4]4--based structural units, as identified through spectroscopic analyses using fourier transform infrared spectroscopy, Raman spectroscopy, and X-ray photoelectron spectroscopy. The electronegativity of the retrieved fluxes was also evaluated since higher electronegativity results in greater absorption of electrons in the arc, resulting in arc condensation towards the center direction. Consequently, deeper penetration could be obtained, where the highest electronegativity was identified to be approximately 0.62 of the corrected optical basicity. Thus, both the thermal conductivity and electronegativity of the welding fluxes were identified to determine the heat transfer phenomenon during flux-cored arc welding.

  13. Effect of Compositional Variation in TiO2-Based Flux-Cored Arc Welding Fluxes on the Thermo-physical Properties and Mechanical Behavior of a Weld Zone

    NASA Astrophysics Data System (ADS)

    Kim, J. B.; Lee, T. H.; Sohn, I.

    2018-07-01

    The effect of compositional variation in TiO2-based flux-cored arc welding fluxes on viscosity, wettability, and electronegativity was studied. The thermo-physical properties of the retrieved fluxes and their relationship with the mechanical properties of the weld zone, including tensile strength and micro-Vickers hardness, after welding were identified. Microstructural observation under similar welding conditions revealed significant grain coarsening at a corrected optical basicity (Λcorr) of 0.62, resulting in reduced strength and hardness due to greater heat transfer. Welding fluxes containing TiO2-based simple structural units should result in greater heat transfer due to the deficiency in complex [AlO4]5-- and [SiO4]4--based structural units, as identified through spectroscopic analyses using fourier transform infrared spectroscopy, Raman spectroscopy, and X-ray photoelectron spectroscopy. The electronegativity of the retrieved fluxes was also evaluated since higher electronegativity results in greater absorption of electrons in the arc, resulting in arc condensation towards the center direction. Consequently, deeper penetration could be obtained, where the highest electronegativity was identified to be approximately 0.62 of the corrected optical basicity. Thus, both the thermal conductivity and electronegativity of the welding fluxes were identified to determine the heat transfer phenomenon during flux-cored arc welding.

  14. A comparative study of three-terminal Hanle signals in CoFe/SiO{sub 2}/n{sup +}-Si and Cu/SiO{sub 2}/n{sup +}-Si tunnel junctions

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    Lee, Jeong-Hyeon; Cho, B. K., E-mail: chobk@gist.ac.kr; Grünberg Center for Magnetic Nanomaterials, Gwangju Institute of Science and Technology

    We performed three-terminal (3T) Hanle measurement for two types of sample series, CoFe/SiO{sub 2}/n{sup +}-Si and Cu/SiO{sub 2}/n{sup +}-Si, with various tunnel resistances. Clear Hanle signal and anomalous scaling between spin resistance-area product and tunnel resistance-area product were observed in CoFe/SiO{sub 2}/n{sup +}-Si devices. In order to explore the origin of the Hanle signal and the impurity-assisted tunneling effect on the Hanle signal in our devices, Hanle measurement in Cu/SiO{sub 2}/n{sup +}-Si devices was performed as well. However, no detectable Hanle signal was observed in Cu/SiO{sub 2}/n{sup +}-Si, even though a lot of samples with various tunnel resistances were studiedmore » in wide temperature and bias voltage ranges. Through a comparative study, it is found that the impurity-assisted tunneling magnetoresistance mechanism would not play a dominant role in the 3T Hanle signal in CoFe/SiO{sub 2}/n{sup +}-Si tunnel junctions, where the SiO{sub 2} was formed by plasma oxidation to minimize impurities.« less

  15. Constraining N2O emissions since 1940 by firn air isotope measurements in both hemispheres

    NASA Astrophysics Data System (ADS)

    Prokopiou, Markella; Martinerie, Patricia; Sapart, Celia; Witrant, Emmanuel; Monteil, Guillaume; Ishijima, Kentaro; Kaiser, Jan; Levin, Ingeborg; Sowers, Todd; Blunier, Thomas; Etheridge, David; Dlugokencky, Ed; van de Wal, Roderik; Röckmann, Thomas

    2017-04-01

    N2O is currently the 3rd most important anthropogenic greenhouse gas in terms of radiative forcing and its atmospheric mole fraction is rising steadily. To quantify the growth rate and its causes, we performed a multi-site reconstruction of the atmospheric N2O mole fraction and isotopic composition using firn air data collected from Greenland and Antarctica in combination with a firn diffusion and densification model. The multi-site reconstruction showed that while the global mean N2O mole fraction increased from (290±1) nmol mol-1 in 1940 to (322±1) nmol mol-1 in 2008 the isotopic δ values of atmospheric N2O decreased by (- 2.2±0.2) ‰ for δ15Nav, (- 1.0±0.3) ‰ for δ18O, (- 1.3±0.6) ‰ for δ15Nα, and (- 2.8±0.6) ‰ for δ15Nβover the same period. The detailed temporal evolution of the mole fraction and isotopic composition derived from the firn air model was then used in a two-box atmospheric model (comprising a stratospheric and a tropospheric box) to infer changes in the isotopic source signature over time. The precise value of the source strength depends on the choice of the N2O lifetime, which we choose to be 123 a. Adopting this lifetime results in total average source isotopic signatures of (- 7.6±0.8) ‰ (vs. Air-N2) for δ15Nav, (32.2±0.2) ‰ (vs. VSMOW) for δ18O, (- 3.0±1.9) ‰ (vs. Air-N2) for δ15Nα, and (- 11.7±2.3) ‰ (vs. Air-N2) for δ15Nβ over the investigated period. δ15Navand δ15Nβ show some temporal variability while the other source isotopic signatures remain unchanged. The 15N site-preference (= δ15Nα - δ15Nβ) can be used to reveal further information on the source emission origins. Based on the changes in the isotopes we conclude that the main contribution to N2O changes in the atmosphere since 1940 is from soils, with agricultural soils being the principal anthropogenic component, which is in line with previous studies.

  16. Human Effects and Soil Surface CO2 fluxes in Tropical Urban Green Areas, Singapore

    NASA Astrophysics Data System (ADS)

    Ng, Bernard; Gandois, Laure; Kai, Fuu Ming; Chua, Amy; Cobb, Alex; Harvey, Charles; Hutyra, Lucy

    2013-04-01

    Urban green spaces are appreciated for their amenity value, with increasing interest in the ecosystem services they could provide (e.g. climate amelioration and increasingly as possible sites for carbon sequestration). In Singapore, turfgrass occupies approximately 20% of the total land area and is readily found on both planned and residual spaces. This project aims at understanding carbon fluxes in tropical urban green areas, including controls of soil environmental factors and the effect of urban management techniques. Given the large pool of potentially labile carbon, management regimes are recognised to have an influence on soil environmental factors (temperature and moisture), this would affect soil respiration and feedbacks to the greenhouse effect. A modified closed dynamic chamber method was employed to measure total soil respiration fluxes. In addition to soil respiration rates, environmental factors such as soil moisture and temperature, and ambient air temperature were monitored for the site in an attempt to evaluate their control on the observed fluxes. Measurements of soil-atmosphere CO2 exchanges are reported for four experimental plots within the Singtel-Kranji Radio Transmission Station (103o43'49E, 1o25'53N), an area dominated by Axonopus compressus. Different treatments such as the removal of turf, and application of clippings were effected as a means to determine the fluxes from the various components (respiration of soil and turf, and decomposition of clippings), and to explore the effects of human intervention on observed effluxes. The soil surface CO2 fluxes observed during the daylight hours ranges from 2.835 + 0.772 umol m-2 s-1 for the bare plot as compared to 6.654 + 1.134 umol m-2 s-1 for the turfed plot; this could be attributed to both autotrophic and heterotrophic respiration. Strong controls of both soil temperature and soil moisture are observed on measured soil fluxes. On the base soils, fluxes were positively correlated to soil

  17. Continuous-flux MOVPE growth of position-controlled N-face GaN nanorods and embedded InGaN quantum wells

    NASA Astrophysics Data System (ADS)

    Bergbauer, W.; Strassburg, M.; Kölper, Ch; Linder, N.; Roder, C.; Lähnemann, J.; Trampert, A.; Fündling, S.; Li, S. F.; Wehmann, H.-H.; Waag, A.

    2010-07-01

    We demonstrate the fabrication of N-face GaN nanorods by metal organic vapour phase epitaxy (MOVPE), using continuous-flux conditions. This is in contrast to other approaches reported so far, which have been based on growth modes far off the conventional growth regimes. For position control of nanorods an SiO2 masking layer with a dense hole pattern on a c-plane sapphire substrate was used. Nanorods with InGaN/GaN heterostructures have been grown catalyst-free. High growth rates up to 25 µm h - 1 were observed and a well-adjusted carrier gas mixture between hydrogen and nitrogen enabled homogeneous nanorod diameters down to 220 nm with aspect ratios of approximately 8:1. The structural quality and defect progression within nanorods were determined by transmission electron microscopy (TEM). Different emission energies for InGaN quantum wells (QWs) could be assigned to different side facets by room temperature cathodoluminescence (CL) measurements.

  18. Continuous-flux MOVPE growth of position-controlled N-face GaN nanorods and embedded InGaN quantum wells.

    PubMed

    Bergbauer, W; Strassburg, M; Kölper, Ch; Linder, N; Roder, C; Lähnemann, J; Trampert, A; Fündling, S; Li, S F; Wehmann, H-H; Waag, A

    2010-07-30

    We demonstrate the fabrication of N-face GaN nanorods by metal organic vapour phase epitaxy (MOVPE), using continuous-flux conditions. This is in contrast to other approaches reported so far, which have been based on growth modes far off the conventional growth regimes. For position control of nanorods an SiO(2) masking layer with a dense hole pattern on a c-plane sapphire substrate was used. Nanorods with InGaN/GaN heterostructures have been grown catalyst-free. High growth rates up to 25 microm h(-1) were observed and a well-adjusted carrier gas mixture between hydrogen and nitrogen enabled homogeneous nanorod diameters down to 220 nm with aspect ratios of approximately 8:1. The structural quality and defect progression within nanorods were determined by transmission electron microscopy (TEM). Different emission energies for InGaN quantum wells (QWs) could be assigned to different side facets by room temperature cathodoluminescence (CL) measurements.

  19. Airborne boundary layer flux measurements of trace species over Canadian boreal forest and northern wetland regions

    NASA Technical Reports Server (NTRS)

    Ritter, John A.; Barrick, John D. W.; Watson, Catherine E.; Sachse, Glen W.; Gregory, Gerald L.; Anderson, Bruce E.; Woerner, Mary A.; Collins, James E., Jr.

    1994-01-01

    Airborne heat, moisture, O3, CO, and CH4 flux measurements were obtained over the Hudson Bay lowlands (HBL) and northern boreal forest regions of Canada during July - August 1990. The airborne flux measurements were an integral part of the NASA/Arctic Boundary Layer Expedition (ABLE) 3B field experiment executed in collaboration with the Canadian Northern Wetlands Study (NOWES). Airborne CH4 flux measurements were taken over a large portion of the HBL. The surface level flux of CH4 was obtained from downward extrapolations of multiple-level CH4 flux measurements. Methane source strengths ranged from -1 to 31 mg m(exp -2)/d, with the higher values occurring in relatively small, isolated areas. Similar measurements of the CH4 source strength in the boreal forest region of Schefferville, Quebec, ranged from 6 to 27 mg m(exp -2)/d and exhibited a diurnal dependence. The CH4 source strengths found during the ABLE 3B expedition were much lower than the seasonally averaged source strength of 51 mg m(exp -2)/d found for the Yukon-Kuskokwim delta region of Alaska during the previous ABLE 3A study. Large positive CO fluxes (0.31 to 0.53 parts per billion by volume (ppbv) m/s) were observed over the inland, forested regions of the HBL study area, although the mechanism for the generation of these fluxes was not identified. Repetitive measurements along the same ground track at various times of day near the Schefferville site also suggested a diurnal dependence for CO emissions. Measurements of surface resistance to the uptake of O3 (1.91 to 0.80 s/cm) for the HBL areas investigated were comparable to those observed near the Schefferville site (3.40 to 1.10 s/cm). Surface resistance values for the ABLE 3B study area were somewhat less than those observed over the Yukon-Kuskokwim delta during the previous ABLE 3A study. The budgets for heat, moisture, O3, CO, and CH4 were evaluated. The residuals from these budget studies indicated, for the cases selected, a moderate net

  20. Effect of granulated wood ash fertilization on N2O emissions in boreal peat forests

    NASA Astrophysics Data System (ADS)

    Liimatainen, Maarit; Martikainen, Pertti J.; Hytönen, Jyrki; Maljanen, Marja

    2016-04-01

    Peatlands cover one third of the land surface area in Finland and over half of that are drained for forestry. Natural peatlands are either small sources of nitrous oxide (N2O) or they can also act as a sinks of N2O. When peatlands are drained, oxygen concentration in the peat increases, organic matter decomposition accelerates and N2O emissions may increase significantly, especially in nutrient rich peat soils. Hence drainage and land-use changes can have a big impact on N2O fluxes in peatlands. The annual consumption of wood chips is to be increased to 13.5 M m3 from the present 8.7 M m3 in Finland. This will also increase the amount of wood ash in the power plants. Wood ash contains considerable amounts of mineral nutrients but lacks nitrogen. Therefore, it has been used as a fertilizer in nitrogen rich peatland forests lacking other nutrients. Recycling of ash would also return the nutrients lost during biomass harvesting back to the forests. We studied the effects of granulated wood ash as a fertilizer in peat soils drained for forestry. Ash is nowadays granulated mainly to facilitate its handling and spreading. Granulation also stabilizes the ash decreasing the solubility of most of the nutrients and minimizing harmful effects of ash spread over the vegetation. Granulated wood ash increases soil pH less than loose ash. Drainage of peatland forests increases microbial activity in the soil which is furthermore intensified with the addition of ash promoting organic matter decomposition and possibly affecting N2O emissions. We studied the effect of granulated wood ash on N2O fluxes in three different peat forests in Finland in both field and laboratory experiments. In the field, N2O emissions were not affected by granulated wood ash fertilization but the soil respiration rate increased. However, in the laboratory studies we observed a clear decrease in N2O production due to wood ash addition, although changes in pH values were only minor. We studied what could

  1. The kinetic friction of ZnO nanowires on amorphous SiO2 and SiN substrates

    NASA Astrophysics Data System (ADS)

    Roy, Aditi; Xie, Hongtao; Wang, Shiliang; Huang, Han

    2016-12-01

    ZnO nanowires were bent on amorphous SiO2 and SiN substrates in an ambient atmosphere using optical nanomanipulation. The kinetic friction between the nanowires and substrate was determined from the bent shape of the nanowires. The kinetic friction force per unit area, i.e. frictional shear stress, for the ZnO/SiO2 and ZnO/SiN nanowire/substrate systems being measured were 1.05 ± 0.28 and 2.08 ± 0.33 MPa, respectively. The surface roughness and the Hamaker constant of SiO2 and SiN substrates had significant effect on the frictional stresses.

  2. Initial assessment of multi-scale measures of C02 and H20 flux in the Siberian taiga

    Treesearch

    D.Y. Hollinger; F.M. Kelliher; E.-D. Schulze; N.N. Vygodskaya; A. Varlagin; I. Milukova; J.N. Byers; A. Sogachov; J.E. Hunt; T.M. McSeveny; K.I. Kobak; G. Bauer; A. Arneth

    1995-01-01

    We measured CO2 and H2O fluxes between undisturbed Larix gmelinii forest and the atmosphere at a remote Eastern Siberian site in July 1993. Scaled-up leaf-level porometer measurements agreed with those derived from the eddy correlation technique for the canopy fluxes of CO2 and H...

  3. Reactions of CH3SH and CH3SSCH3 with gas-phase hydrated radical anions (H2O)n(•-), CO2(•-)(H2O)n, and O2(•-)(H2O)n.

    PubMed

    Höckendorf, Robert F; Hao, Qiang; Sun, Zheng; Fox-Beyer, Brigitte S; Cao, Yali; Balaj, O Petru; Bondybey, Vladimir E; Siu, Chi-Kit; Beyer, Martin K

    2012-04-19

    The chemistry of (H(2)O)(n)(•-), CO(2)(•-)(H(2)O)(n), and O(2)(•-)(H(2)O)(n) with small sulfur-containing molecules was studied in the gas phase by Fourier transform ion cyclotron resonance mass spectrometry. With hydrated electrons and hydrated carbon dioxide radical anions, two reactions with relevance for biological radiation damage were observed, cleavage of the disulfide bond of CH(3)SSCH(3) and activation of the thiol group of CH(3)SH. No reactions were observed with CH(3)SCH(3). The hydrated superoxide radical anion, usually viewed as major source of oxidative stress, did not react with any of the compounds. Nanocalorimetry and quantum chemical calculations give a consistent picture of the reaction mechanism. The results indicate that the conversion of e(-) and CO(2)(•-) to O(2)(•-) deactivates highly reactive species and may actually reduce oxidative stress. For reactions of (H(2)O)(n)(•-) with CH(3)SH as well as CO(2)(•-)(H(2)O)(n) with CH(3)SSCH(3), the reaction products in the gas phase are different from those reported in the literature from pulse radiolysis studies. This observation is rationalized with the reduced cage effect in reactions of gas-phase clusters. © 2012 American Chemical Society

  4. The Nitrous Oxide (N2O) Budget: Constraints from Atmospheric Observations and Models

    NASA Astrophysics Data System (ADS)

    Tian, H.; Thompson, R.; Canadell, J.; Winiwarter, W.; Tian, H.; Thompson, R.; Prather, M. J.

    2017-12-01

    The increasing global abundance of N2O poses a threat to human health and society over this coming century through both climate change and ozone depletion. In the sense of greenhouse gases, N2O ranks third behind CO2 and CH4. In the sense of ozone depletion, N2O stands alone. In order to identify the cause of these increases and hopefully reverse them, we need to have a thorough understanding of the sources and sinks (a.k.a. the budget) of N2O and how they can be altered. A bottom-up approach to the budget evaluates individual biogeochemical sources of N2O from the land and ocean; whereas, a top-down approach uses atmospheric observations of the variability, combined with modeling of the atmospheric chemistry and transport, to infer the magnitude of sources and sinks throughout the Earth system. This paper reviews top-down approaches using atmospheric data; a similar top-down approach can be taken with oceanic measurements of N2O, but is not covered here. Stratospheric chemistry is the predominant loss of N2O, and here we review how a merging of new measurements with stratospheric chemistry models is able to provide a constrained budget for the global N2O sink. N2O surface sources are transported and mixed throughout the atmosphere, providing positive anomalies in the N2O abundance (mole fraction of N2O with respect to dry air); while N2O-depleted air from the stratosphere provides negative anomalies. With accurate atmospheric transport models, including for stratosphere-troposphere exchange, the observed tropospheric variability in N2O is effectively a fingerprint of the location and magnitude of sources. This inverse modeling of sources is part of the top-down constraints and is reviewed here.

  5. Long-term nitrous oxide fluxes in annual and perennial agricultural and unmanaged ecosystems in the upper Midwest USA.

    PubMed

    Gelfand, Ilya; Shcherbak, Iurii; Millar, Neville; Kravchenko, Alexandra N; Robertson, G Philip

    2016-11-01

    Differences in soil nitrous oxide (N 2 O) fluxes among ecosystems are often difficult to evaluate and predict due to high spatial and temporal variabilities and few direct experimental comparisons. For 20 years, we measured N 2 O fluxes in 11 ecosystems in southwest Michigan USA: four annual grain crops (corn-soybean-wheat rotations) managed with conventional, no-till, reduced input, or biologically based/organic inputs; three perennial crops (alfalfa, poplar, and conifers); and four unmanaged ecosystems of different successional age including mature forest. Average N 2 O emissions were higher from annual grain and N-fixing cropping systems than from nonleguminous perennial cropping systems and were low across unmanaged ecosystems. Among annual cropping systems full-rotation fluxes were indistinguishable from one another but rotation phase mattered. For example, those systems with cover crops and reduced fertilizer N emitted more N 2 O during the corn and soybean phases, but during the wheat phase fluxes were ~40% lower. Likewise, no-till did not differ from conventional tillage over the entire rotation but reduced emissions ~20% in the wheat phase and increased emissions 30-80% in the corn and soybean phases. Greenhouse gas intensity for the annual crops (flux per unit yield) was lowest for soybeans produced under conventional management, while for the 11 other crop × management combinations intensities were similar to one another. Among the fertilized systems, emissions ranged from 0.30 to 1.33 kg N 2 O-N ha -1  yr -1 and were best predicted by IPCC Tier 1 and ΔEF emission factor approaches. Annual cumulative fluxes from perennial systems were best explained by soil NO3- pools (r 2  = 0.72) but not so for annual crops, where management differences overrode simple correlations. Daily soil N 2 O emissions were poorly predicted by any measured variables. Overall, long-term measurements reveal lower fluxes in nonlegume perennial vegetation and, for

  6. Site-specific 15N isotopic signatures of abiotically produced N2O

    NASA Astrophysics Data System (ADS)

    Heil, Jannis; Wolf, Benjamin; Brüggemann, Nicolas; Emmenegger, Lukas; Tuzson, Béla; Vereecken, Harry; Mohn, Joachim

    2014-08-01

    Efficient nitrous oxide (N2O) mitigation strategies require the identification of the main source and sink processes and their contribution to total soil N2O production. Several abiotic reactions of nitrification intermediates leading to N2O production are known, but their contribution to total N2O production in soils is uncertain. As the site preference (SP) of 15N in N2O is a promising tool to give more insight into N2O production processes, we investigated the SP of N2O produced by different abiotic reactions in a laboratory study. All reactions involved the nitrification intermediate hydroxylamine (NH2OH) in combination with nitrite (NO2-), Fe3+, Fe2+ and Cu2+, reactants commonly or potentially found in soils, at different concentrations and pH values. N2O production and its four main isotopic species (14N14N16O, 15N14N16O, 14N15N16O, and 14N14N18O) were quantified simultaneously and online at high temporal resolution using quantum cascade laser absorption spectroscopy. Thereby, our study presents the first continuous analysis of δ18O in N2O. The experiments revealed the possibility of purely abiotic reactions over a wide range of acidity (pH 3-8) by different mechanisms. All studied abiotic pathways produced N2O with a characteristic SP in the range of 34-35‰, unaffected by process conditions and remaining constant over the course of the experiments. These findings reflect the benefit of continuous N2O isotopic analysis by laser spectroscopy, contribute new information to the challenging source partitioning of N2O emissions from soils, and emphasize the potentially significant role of coupled biotic-abiotic reactions in soils.

  7. Detection of stratospheric N2O5 by infrared remote sounding

    NASA Technical Reports Server (NTRS)

    Toon, G. C.; Farmer, C. B.; Norton, R. H.

    1986-01-01

    Measurements of N2O5 absorption (1230 and 1260 per cm) in infrared spectra were carried out using the Atmospheric Trace Molecule Spectroscopy (ATMOS) instruments on board Spacelab 3. The detection of stratospheric N2O5, a temporary reservoir species whose photolysis products catalyze ozone destruction, was confirmed. Preliminary analysis of spectra recorded at sunrise on 1 May 1985 indicates a peak volume mixing ratio of 1.6 x 10 the -9th at 35 km an altitude of 35 km, or a broad concentration peak pf 4 x 10 to the 8th molecules per cu cm between 21 and 35 km. Absorption was not detected in spectra measured at sunset due to the depletion of N2O5 by photolysis during the day. The volume mixing ratio profile of N2O5 between 0 and 75 km altitude is reproduced in graphic form.

  8. Constraining N2O emissions since 1940 using firn air isotope measurements in both hemispheres

    NASA Astrophysics Data System (ADS)

    Prokopiou, Markella; Martinerie, Patricia; Sapart, Célia J.; Witrant, Emmanuel; Monteil, Guillaume; Ishijima, Kentaro; Bernard, Sophie; Kaiser, Jan; Levin, Ingeborg; Blunier, Thomas; Etheridge, David; Dlugokencky, Ed; van de Wal, Roderik S. W.; Röckmann, Thomas

    2017-04-01

    N2O is currently the third most important anthropogenic greenhouse gas in terms of radiative forcing and its atmospheric mole fraction is rising steadily. To quantify the growth rate and its causes over the past decades, we performed a multi-site reconstruction of the atmospheric N2O mole fraction and isotopic composition using new and previously published firn air data collected from Greenland and Antarctica in combination with a firn diffusion and densification model. The multi-site reconstruction showed that while the global mean N2O mole fraction increased from (290 ± 1) nmol mol-1 in 1940 to (322 ± 1) nmol mol-1 in 2008, the isotopic composition of atmospheric N2O decreased by (-2.2 ± 0.2) ‰ for δ15Nav, (-1.0 ± 0.3) ‰ for δ18O, (-1.3 ± 0.6) ‰ for δ15Nα, and (-2.8 ± 0.6) ‰ for δ15Nβ over the same period. The detailed temporal evolution of the mole fraction and isotopic composition derived from the firn air model was then used in a two-box atmospheric model (comprising a stratospheric box and a tropospheric box) to infer changes in the isotopic source signature over time. The precise value of the source strength depends on the choice of the N2O lifetime, which we choose to fix at 123 years. The average isotopic composition over the investigated period is δ15Nav = (-7.6 ± 0.8) ‰ (vs. air-N2), δ18O = (32.2 ± 0.2) ‰ (vs. Vienna Standard Mean Ocean Water - VSMOW) for δ18O, δ15Nα = (-3.0 ± 1.9) ‰ and δ15Nβ = (-11.7 ± 2.3) ‰. δ15Nav, and δ15Nβ show some temporal variability, while for the other signatures the error bars of the reconstruction are too large to retrieve reliable temporal changes. Possible processes that may explain trends in 15N are discussed. The 15N site preference ( = δ15Nα - δ15Nβ) provides evidence of a shift in emissions from denitrification to nitrification, although the uncertainty envelopes are large.

  9. Detection of interstellar N2O: A new molecule containing an N-O bond

    NASA Astrophysics Data System (ADS)

    Ziurys, L. M.; Apponi, A. J.; Hollis, J. M.; Snyder, L. E.

    1994-12-01

    A new interstellar molecule, N2O, known as nitrous oxide or 'laughing gas,' has been detected using the NRAO 12 m telescope. The J = 3 - 2, 4 - 3, 5 - 4, and 6 - 5 rotational transitions of this species at 75, 100, 125, and 150 GHz, respectively, were observed toward Sgr B2(M). The column density derived for N2O in this source is Ntot approx. 1015/sq. cm, which corresponds to a fractional abundance of approx. 10-9, relative to H2. This value implies abundance ratios of N2O/NO approx. 0.1 and N2O/HNO approx. 3 in the Galactic center. Such ratios are in excellent agreement with predictions of ion-molecule models of interstellar chemistry using early-time calculations and primarily neutral-neutral reactions. N2O is the third interstellar molecule detected thus far containing an N-O bond. Such bonds cannot be so rare as previously thought.

  10. Investigation of Defect Distributions in SiO2/AlGaN/GaN High-Electron-Mobility Transistors by Using Capacitance-Voltage Measurement with Resonant Optical Excitation

    NASA Astrophysics Data System (ADS)

    Kim, Tae-Soo; Lim, Seung-Young; Park, Yong-Keun; Jung, Gunwoo; Song, Jung-Hoon; Cha, Ho-Young; Han, Sang-Woo

    2018-06-01

    We investigated the distributions and the energy levels of defects in SiO2/AlGaN/GaN highelectron-mobility transistors (HEMTs) by using frequency-dependent ( F- D) capacitance-voltage ( C- V) measurements with resonant optical excitation. A Schottky barrier (SB) and a metal-oxidesemiconductor (MOS) HEMT were prepared to compare the effects of defects in their respective layers. We also investigated the effects of those layers on the threshold voltage ( V th ). A drastic voltage shift in the C- V curve at higher frequencies was caused by the large number of defect levels in the SiO2/GaN interface. A significant shift in V th with additional light illumination was observed due to a charging of the defect states in the SiO2/GaN interface. The voltage shifts were attributed to the detrapping of defect states at the SiO2/GaN interface.

  11. Crystal structure of aqua-1κO-{μ-2-[(2-hydroxy­ethyl)methylamino]ethanolato-2:1κ4 O 1,N,O 2:O 1}[μ-2,2′-(methylimino)diethanolato-1:2κ4 O,N,O′:O]dithiocyanato-1κN,2κN-chromium(III)copper(II)

    PubMed Central

    Rusanova, Julia A.; Semenaka, Valentina V.; Dyakonenko, Viktoriya V.; Shishkin, Oleg V.

    2015-01-01

    The title compound, [CrCu(C5H11NO2)(C5H12NO2)(NCS)2(H2O)] or [Cr(μ-mdea)Cu(μ-Hmdea)(NCS)2H2O], (where mdeaH2 is N-methylethanolamine, C5H13NO2) is formed as a neutral heterometal CuII/CrIII complex. The mol­ecular structure of the complex is based on a binuclear {CuCr(μ-O)2} core. The coordination environment of each metal atom involves the N,O,O atoms of the tridentate ligand, one bridging O atom of the ligand and the N atom of the thio­cyanato ligands. The CuII ion adopts a distorted square-pyramidal coordination while the CrIII ion has a distorted octa­hedral coordination geometry completed by the aqua ligand. In the crystal, the binuclear complexes are linked via two pairs of O—H⋯O hydrogen bonds to form inversion dimers, which are arranged in columns parallel to the a axis. In the μ-mdea ligand two –CH2 groups and the methyl group were refined as disordered over two sets of sites with equal occupancies. The structure was refined as a two-component twin with a twin scale factor of 0.242 (1). PMID:26396853

  12. Characterization of Water Coordination to Ferrous Nitrosyl Complexes with fac-N2O, cis-N2O2, and N2O3 Donor Ligands.

    PubMed

    McCracken, John; Cappillino, Patrick J; McNally, Joshua S; Krzyaniak, Matthew D; Howart, Michael; Tarves, Paul C; Caradonna, John P

    2015-07-06

    Electron paramagnetic resonance (EPR) experiments were done on a series of S = (3)/2 ferrous nitrosyl model complexes prepared with chelating ligands that mimic the 2-His-1-carboxylate facial triad iron binding motif of the mononuclear nonheme iron oxidases. These complexes formed a comparative family, {FeNO}(7)(N2Ox)(H2O)3-x with x = 1-3, where the labile coordination sites for the binding of NO and solvent water were fac for x = 1 and cis for x = 2. The continuous-wave EPR spectra of these three complexes were typical of high-spin S = (3)/2 transition-metal ions with resonances near g = 4 and 2. Orientation-selective hyperfine sublevel correlation (HYSCORE) spectra revealed cross peaks arising from the protons of coordinated water in a clean spectral window from g = 3.0 to 2.3. These cross peaks were absent for the {FeNO}(7)(N2O3) complex. HYSCORE spectra were analyzed using a straightforward model for defining the spin Hamiltonian parameters of bound water and showed that, for the {FeNO}(7)(N2O2)(H2O) complex, a single water conformer with an isotropic hyperfine coupling, Aiso = 0.0 ± 0.3 MHz, and a dipolar coupling of T = 4.8 ± 0.2 MHz could account for the data. For the {FeNO}(7)(N2O)(H2O)2 complex, the HYSCORE cross peaks assigned to coordinated water showed more frequency dispersion and were analyzed with discrete orientations and hyperfine couplings for the two water molecules that accounted for the observed orientation-selective contour shapes. The use of three-pulse electron spin echo envelope modulation (ESEEM) data to quantify the number of water ligands coordinated to the {FeNO}(7) centers was explored. For this aspect of the study, HYSCORE spectra were important for defining a spectral window where empirical integration of ESEEM spectra would be the most accurate.

  13. Nightside electron flux measurements at Mars by the Phobos-2 HARP instrument

    NASA Technical Reports Server (NTRS)

    Shutte, N.; Gringauz, K.; Kiraly, P.; Kotova, G.; Nagy, A. F.; Rosenbauer, H.; Szego, K.; Verigin, M.

    1995-01-01

    All the available nightside electron data obtained during circular orbits at Mars from the Phobos-2 Hyperbolic Retarded Potential Analyzer (HARP) instrument have been examined in detail and are summarized in this paper. An electron flux component with energies exceeding that of the unperturbed solar wind was observed inside the magnetosheath, indicating the presence of acceleration mechanism(s). The character of the electron fluxes measured in the magnetotail cannot be classified in any simple manner, however, there is a correlation between the electron fluxes measured well inside this region and the unperturbed solar wind ram pressure.

  14. Temperature of nitrogen ice on Pluto and its implications for flux measurements.

    PubMed

    Tryka, K A; Brown, R H; Cruikshank, D P; Owen, T C; Geballe, T R; DeBergh, C

    1994-01-01

    Previous work by K.A. Tryka et al. (Science 261, 751-754, 1993) has shown that the profile of the 2.148-micrometers band of solid nitrogen can be used as a "thermometer" and determined the temperature of nitrogen ice on Triton to be 38(+2)-1 K. Here we reevaluate that data and refine the temperature value to 38 +/- 1 K. Applying the same technique to Pluto we determine that the temperature of the N2 ice on that body is 40 +/- 2 K. Using this result we have created a nonisothermal flux model of the Pluto-Charon system. The model treats Pluto as a body with symmetric N2 polar caps and an equatorial region devoid of N2. Comparison with the infrared and millimeter flux measurements shows that the published fluxes are consistent with models incorporating extensive N2 polar caps (down to +/- 15 degrees or +/- 20 degrees latitude) and an equatorial region with a bolometric albedo < or = 0.2.

  15. Temperature of nitrogen ice on Pluto and its implications for flux measurements

    NASA Technical Reports Server (NTRS)

    Tryka, Kimberly A.; Brown, Robert H.; Chruikshank, Dale P.; Owen, Tobias C.; Geballe, Thomas R.; Debergh, Catherine

    1994-01-01

    Previous work by K. A. Tryka et al. (1993) has shown that the profile of the 2.148-micron band of solid nitrogen can be used as a 'thermometer' and determined the tempertature of nitrogen ice on Triton to be 38(sup +2)(sub -1) K. Here we reevalute that data and refine the temperature value to 38 +/- 1 K. Applying the same technique to Pluto we determine that the temperature of the N2 ice on that body is 40 +/- 2 K. Using this result we have created a nonisothermal flux model of the Pluto-Charon system. The model treats Pluto as a body with symmetric N2 polar caps and an equatorial region devoid of N2. Comparison with the infrared and millimeter flux measurements shows that the published fluxes are consistent with models incorporating extensive N2 polar caps (down to +/- 15 deg ot +/- 20 deg latitude) and an equatorial region with a bolometric albedo less than or equal to 0.2.

  16. Development of atmospheric N2O isotopomers model based on a chemistry-coupled atmospheric general circulation model

    NASA Astrophysics Data System (ADS)

    Ishijima, K.; Toyoda, S.; Sudo, K.; Yoshikawa, C.; Nanbu, S.; Aoki, S.; Nakazawa, T.; Yoshida, N.

    2009-12-01

    It is well known that isotopic information is useful to qualitatively understand cycles and constrain sources of some atmospheric species, but so far there has been no study to model N2O isotopomers throughout the atmosphere from the troposphere to the stratosphere, including realistic surface N2O isotopomers emissions. We have started to develop a model to simulate spatiotemporal variations of the atmospheric N2O isotopomers in both the troposphere and the stratosphere, based on a chemistry-coupled atmospheric general circulation model, in order to obtain more accurate quantitative understanding of the global N2O cycle. For surface emissions of the isotopomers, combination of EDGAR-based anthropogenic and soil fluxes and monthly varying GEIA oceanic fluxes are factored, using isotopic values of global total sources estimated from firn-air analyses based long-term trend of the atmospheric N2O isotopomers. Isotopic fractionations in chemical reactions are considered for photolysis and photo-oxidation of N2O in the stratosphere. The isotopic fractionation coefficients have been employed from studies based on laboratory experiments, but we also will test the coefficients determined by theoretical calculations. In terms of the global N2O isotopomer budgets, precise quantification of the sources is quite challenging, because even the spatiotemporal variabilities of N2O sources have never been adequately estimated. Therefore, we have firstly started validation of simulated isotopomer results in the stratosphere, by using the isotopomer profiles obtained by balloon observations. N2O concentration profiles are mostly well reproduced, partly because of realistic reproduction of dynamical processes by nudging with reanalysis meteorological data. However, the concentration in the polar vortex tends to be overestimated, probably due to relatively coarse wave-length resolution in photolysis calculation. Such model features also appear in the isotopomers results, which are

  17. Diffusivity in surficial sediments and benthic mats determined by use of a combined N 2O-O 2 microsensor

    NASA Astrophysics Data System (ADS)

    Glud, Ronnie Nøhr; Jensen, Kim; Revsbech, Niels Peter

    1995-01-01

    Diffusional characteristics of two biologically active surface sediments were determined by use of a combined N 2O-O 2 microsensor. By analyzing changes in the N2O-gradients in these sediments, it was possible to determine the product ( φDs) for this species with submillimetre depth resolution, where φ is the porosity and Ds the substrate diffusion coefficient. The ( φDs)-value for O 2 could be calculated then from ( φDs)-value for N 2O, because the diffusivity of the two molecules were modified in the same way within the sediment. Both sediments exhibited fine-scale horizontal and vertical variability in diffusion characteristics, and this must be accounted for when analyzing microprofile data. The average ( φDs)-value for N 2O at 20°C for an estuarine surface sediment was 0.93 × 10 -5 cm2 s -1 (at 0-4 mm depth), while the value for the upper 2 mm of a stream sediment covered by a microbial mat was 1.42 × 10 -5 cm 2 s -1. Biological inactivation and oxidation by exposure to an O 2 atmosphere had no effect on the measured ( φDs) for the estuarine sediment; however, the value for the sediment covered by a microbial mat, with dense populations of meiofauna, decreased by 20%. The method presented is ideal for measurements of diffusivity at a high spatial resolution in surficial sediments and densely packed microbial communities.

  18. Standardized Automated CO2/H2O Flux Systems for Individual Research Groups and Flux Networks

    NASA Astrophysics Data System (ADS)

    Burba, George; Begashaw, Israel; Fratini, Gerardo; Griessbaum, Frank; Kathilankal, James; Xu, Liukang; Franz, Daniela; Joseph, Everette; Larmanou, Eric; Miller, Scott; Papale, Dario; Sabbatini, Simone; Sachs, Torsten; Sakai, Ricardo; McDermitt, Dayle

    2017-04-01

    models, and the improvements focused on increased stability in the presence of contamination, refining temperature control and compensation, and providing more accurate fast gas concentration measurements. In terms of the flux calculations, improvements focused on automating the on-site flux calculations using EddyPro® software run by a weatherized fully digital microcomputer, SmartFlux2. In terms of site management and data sharing, the development focused on web-based software, FluxSuite, which allows real-time station monitoring and data access by multiple users. The presentation will describe details for the key developments and will include results from field tests of the RS gas analyzer models in comparison with older models and control reference instruments.

  19. Potentials and challenges associated with automated closed dynamic chamber measurements of soil CO2 fluxes

    NASA Astrophysics Data System (ADS)

    Görres, Carolyn-Monika; Kammann, Claudia; Ceulemans, Reinhart

    2015-04-01

    Soil respiration fluxes are influenced by natural factors such as climate and soil type, but also by anthropogenic activities in managed ecosystems. As a result, soil CO2 fluxes show a large intra- and interannual as well as intra- and intersite variability. Most of the available soil CO2 flux data giving insights into this variability have been measured with manually closed static chambers, but technological advances in the past 15 years have also led to an increased use of automated closed chamber systems. The great advantage of automated chambers in comparison to manually operated chambers is the higher temporal resolution of the flux data. This is especially important if we want to better understand the effects of short-term events, e.g. fertilization or heavy rainfall, on soil CO2 flux variability. However, the chamber method is an invasive measurement method which can potentially alter soil CO2 fluxes and lead to biased measurement results. In the peer-reviewed literature, many papers compare the field performance and results of different closed static chamber designs, or compare manual chambers with automated chamber systems, to identify potential biases in CO2 flux measurements, and thus help to reduce uncertainties in the flux data. However, inter-comparisons of different automated closed dynamic chamber systems are still lacking. Here we are going to present a field comparison of the most-cited automated chamber system, the LI-8100A Automated Soil Flux System, with the also commercially available Greenhouse Gas Monitoring System AGPS. Both measurement systems were installed side by side at a recently harvested poplar bioenergy plantation (POPFULL, http://uahost.uantwerpen.be/popfull/) from April 2014 until August 2014. The plantation provided optimal comparison conditions with a bare field situation after the harvest and a regrowing canopy resulting in a broad variety of microclimates. Furthermore, the plantation was planted in a double-row system with

  20. Gas entrapment and microbial N2O reduction reduce N2O emissions from a biochar-amended sandy clay loam soil

    PubMed Central

    Harter, Johannes; Guzman-Bustamante, Ivan; Kuehfuss, Stefanie; Ruser, Reiner; Well, Reinhard; Spott, Oliver; Kappler, Andreas; Behrens, Sebastian

    2016-01-01

    Nitrous oxide (N2O) is a potent greenhouse gas that is produced during microbial nitrogen transformation processes such as nitrification and denitrification. Soils represent the largest sources of N2O emissions with nitrogen fertilizer application being the main driver of rising atmospheric N2O concentrations. Soil biochar amendment has been proposed as a promising tool to mitigate N2O emissions from soils. However, the underlying processes that cause N2O emission suppression in biochar-amended soils are still poorly understood. We set up microcosm experiments with fertilized, wet soil in which we used 15N tracing techniques and quantitative polymerase chain reaction (qPCR) to investigate the impact of biochar on mineral and gaseous nitrogen dynamics and denitrification-specific functional marker gene abundance and expression. In accordance with previous studies our results showed that biochar addition can lead to a significant decrease in N2O emissions. Furthermore, we determined significantly higher quantities of soil-entrapped N2O and N2 in biochar microcosms and a biochar-induced increase in typical and atypical nosZ transcript copy numbers. Our findings suggest that biochar-induced N2O emission mitigation is based on the entrapment of N2O in water-saturated pores of the soil matrix and concurrent stimulation of microbial N2O reduction resulting in an overall decrease of the N2O/(N2O + N2) ratio. PMID:28008997

  1. Bis(2,2'-bipyridyl-κN,N')(carbonato-κO,O')cobalt(III) bromide trihydrate.

    PubMed

    Ma, Peng-Tao; Wang, Yu-Xia; Zhang, Guo-Qian; Li, Ming-Xue

    2007-12-06

    The title complex, [Co(CO(3))(C(10)H(8)N(2))(2)]Br·3H(2)O, is isostructural with the chloride analogue. The six-coordinated octahedral [Co(2,2'-bipy)(2)CO(3)](+) cation (2,2'-bipy is 2,2'-bipyrid-yl), bromide ion and water mol-ecules are linked together via O-H⋯Br and O-H⋯O hydrogen bonds, generating a one-dimensional chain.

  2. In Situ Measurements of N2O and CH4 During SOLVE on the ER-2 Using a New Tunable Diode Laser Instrument

    NASA Technical Reports Server (NTRS)

    Jost, Hansjurg

    2002-01-01

    This report is the final report for Cooperative Agreement NCC2-1105: 'In Situ Measurements of N2O and CH4 during SOLVE on the ER-2 using a new tunable diode laser instrument.' The tasks outlined in the proposal are listed below with a brief comment. The publications and the conference presentations are listed. Finally the important publications are attached. The Cooperative Agreement made possible a research effort to produce high precision and high accuracy in situ measurements of methane and nitrous oxide on the ER-2 during the SOLVE field campaign and to analyze these measurements. These measurements of CH4 and N2O were of utmost importance to studies of the ozone losses in the Arctic winter and spring. The concentrations measured over a large spatial and temporal range allowed the separation of the dynamical and chemical ozone loss. The most important results of the SOLVE program were contained in two scientific papers. This Cooperative Agreement allowed the participation of the Argus instrument in the program and the analysis of the data.

  3. Net ecosystem exchange of CO2 and H2O fluxes from irrigated grain sorghum and maize in the Texas High Plains.

    PubMed

    Wagle, Pradeep; Gowda, Prasanna H; Moorhead, Jerry E; Marek, Gary W; Brauer, David K

    2018-05-08

    Net ecosystem exchange (NEE) of carbon dioxide (CO 2 ) and water vapor (H 2 O) fluxes from irrigated grain sorghum (Sorghum bicolor L. Moench) and maize (Zea mays L.) fields in the Texas High Plains were quantified using the eddy covariance (EC) technique during 2014-2016 growing seasons and examined in terms of relevant controlling climatic variables. Eddy covariance measured evapotranspiration (ET EC ) was also compared against lysimeter measured ET (ET Lys ). Daily peak (7-day averages) NEE reached approximately -12 g C m -2 for sorghum and -14.78 g C m -2 for maize. Daily peak (7-day averages) ET EC reached approximately 6.5 mm for sorghum and 7.3 mm for maize. Higher leaf area index (5.7 vs 4-4.5 m 2  m -2 ) and grain yield (14 vs 8-9 t ha -1 ) of maize compared to sorghum caused larger magnitudes of NEE and ET EC in maize. Comparisons of ET EC and ET Lys showed a strong agreement (R 2  = 0.93-0.96), while the EC system underestimated ET by 15-24% as compared to lysimeter without any corrections or energy balance adjustments. Both NEE and ET EC were not inhibited by climatic variables during peak photosynthetic period even though diurnal peak values (~2-weeks average) of photosynthetic photon flux density (PPFD), air temperature (T a ), and vapor pressure deficit (VPD) had reached over 2000 μmol m -2  s -1 , 30 °C, and 2.5 kPa, respectively, indicating well adaptation of both C 4 crops in the Texas High Plains under irrigation. However, more sensitivity of NEE and H 2 O fluxes beyond threshold T a and VPD for maize than for sorghum indicated higher adaptability of sorghum for the region. These findings provide baseline information on CO 2 fluxes and ET for a minimally studied grain sorghum and offer a robust geographic comparison for maize outside the United States Corn Belt. However, longer-term measurements are required for assessing carbon and water dynamics of these globally important agro-ecosystems. Copyright

  4. Measurements of N2O and SF6 mole fraction between 1977 and 1998 in archived air samples from Cape Meares, Oregon

    NASA Astrophysics Data System (ADS)

    Rolfe, T.; Rice, A. L.; Radda, J.

    2015-12-01

    The quantification of greenhouse gas concentrations in the atmosphere is important for monitoring imbalances in their global budgets between sources and sinks and their changes in time. Nitrous oxide (N2O) is a strong radiative trace gas with a GWP of ~300 times CO2 over a 100 year period and an atmospheric lifetime of ~100 years. The preindustrial revolution background concentration of N2O was ~270 ppb. Today, the concentration is ~330 ppb. Sulfur hexafluoride (SF6) is another potent greenhouse gas with a long lifetime (800 to 3200 years) and very large GWP (~23000 times CO2 over a 100 year period). Its current atmospheric concentration is low (~8 ppt today). Direct measurements of N2O and SF6 in air prior to the mid-1990s are few. Over 200 archived atmospheric gas samples collected at Cape Meares, Oregon between 1977 and 1998 were analyzed for their N2O and SF6 concentrations using an Agilent (model 6890 N) gas chromatograph fitted with an electron capture detector using a two column "heart-cut" technique. Precision of measurement of N2O and SF6 is calculated at 0.13% (1σ) and 1.35% (1σ) respectively. N2O concentrations in the late 1970s and early 1980s average around 303 ppb, rising to 309 ppb in the early 1990s. Between 1980 and 1990, the increase in N2O concentrations is found to be ~0.5 ppb/yr. SF6 concentrations during the late 1970s and early 1980s average around 0.9 ppt and rise slowly, reaching 1.6 ppt in the 1990s. We find that the increase in SF6 between 1980 and 1990 to be ~0.07 ppt/yr. We also discuss sample integrity in storage and observed temporal trends of N2O and SF6.

  5. Field Measurements of Respiratory Del13CO2 and Photodegradation

    NASA Astrophysics Data System (ADS)

    van Asperen, H.; Sabbatini, S.; Nicolini, G.; Warneke, T.; Papale, D.; Notholt, J.

    2014-12-01

    Carbon decomposition dynamics have been studied in a variety of ecosystems and its variation can mostly be explained in terms of environmental variables (e.g. temperature and precipitation). However, carbon dynamics in arid, water limited regions have shown to be very different and are still largely unknown. Several studies have indicated the importance of photodegradation, the direct breakdown of organic matter by sunlight, in these arid regions. A FTIR (Fourier Transform Infrared Spectrometer) was set up to continuously measure concentrations of CO2, CH4, N2O, CO as well as del13C in CO2. The FTIR was connected to 2 different flux measurement systems: a Flux Gradient system and 2 flux chambers, providing a continuous data set of gas concentrations and biosphere-atmosphere gas fluxes at different heights and scales. Field measurements showed photodegradation induced carbon fluxes. Also, respiratory del13CO2 was determined by use of Keeling plots, and was determined to vary between -25‰ and -21‰. A clear diurnal pattern in respiratory del13CO2 was found, suggesting either different (dominant) respiratory processes between day and night or the effect of diffusive fractionation.

  6. Measurement of a surface heat flux and temperature

    NASA Astrophysics Data System (ADS)

    Davis, R. M.; Antoine, G. J.; Diller, T. E.; Wicks, A. L.

    1994-04-01

    The Heat Flux Microsensor is a new sensor which was recently patented by Virginia Tech and is just starting to be marketed by Vatell Corp. The sensor is made using the thin-film microfabrication techniques directly on the material that is to be measured. It consists of several thin-film layers forming a differential thermopile across a thermal resistance layer. The measured heat flux q is proportional to the temperature difference across the resistance layer q= k(sub g)/delta(sub g) x (t(sub 1) - T(sub 2)), where k(sub g) is the thermal conductivity and delta (sub g) is the thickness of the thermal resistance layer. Because the gages are sputter coated directly onto the surface, their total thickness is less than 2 micrometers, which is two orders of magnitude thinner than previous gages. The resulting temperature difference across the thermal resistance layer (delta is less than 1 micrometer) is very small even at high heat fluxes. To generate a measurable signal many thermocouple pairs are put in series to form a differential thermopile. The combination of series thermocouple junctions and thin-film design creates a gage with very attractive characteristics. It is not only physically non-intrusive to the flow, but also causes minimal disruption of the surface temperature. Because it is so thin, the response time is less than 20 microsec. Consequently, the frequency response is flat from 0 to over 50 kHz. Moreover, the signal of the Heat Flux Microsensor is directly proportional to the heat flux. Therefore, it can easily be used in both steady and transient flows, and it measures both the steady and unsteady components of the surface heat flux. A version of the Heat Flux Microsensor has been developed to meet the harsh demands of combustion environments. These gages use platinum and platinum-10 percent rhodium as the thermoelectric materials. The thermal resistance layer is silicon monoxide and a protective coating of Al2O3 is deposited on top of the sensor. The

  7. Measurement of a surface heat flux and temperature

    NASA Technical Reports Server (NTRS)

    Davis, R. M.; Antoine, G. J.; Diller, T. E.; Wicks, A. L.

    1994-01-01

    The Heat Flux Microsensor is a new sensor which was recently patented by Virginia Tech and is just starting to be marketed by Vatell Corp. The sensor is made using the thin-film microfabrication techniques directly on the material that is to be measured. It consists of several thin-film layers forming a differential thermopile across a thermal resistance layer. The measured heat flux q is proportional to the temperature difference across the resistance layer q= k(sub g)/delta(sub g) x (t(sub 1) - T(sub 2)), where k(sub g) is the thermal conductivity and delta (sub g) is the thickness of the thermal resistance layer. Because the gages are sputter coated directly onto the surface, their total thickness is less than 2 micrometers, which is two orders of magnitude thinner than previous gages. The resulting temperature difference across the thermal resistance layer (delta is less than 1 micrometer) is very small even at high heat fluxes. To generate a measurable signal many thermocouple pairs are put in series to form a differential thermopile. The combination of series thermocouple junctions and thin-film design creates a gage with very attractive characteristics. It is not only physically non-intrusive to the flow, but also causes minimal disruption of the surface temperature. Because it is so thin, the response time is less than 20 microsec. Consequently, the frequency response is flat from 0 to over 50 kHz. Moreover, the signal of the Heat Flux Microsensor is directly proportional to the heat flux. Therefore, it can easily be used in both steady and transient flows, and it measures both the steady and unsteady components of the surface heat flux. A version of the Heat Flux Microsensor has been developed to meet the harsh demands of combustion environments. These gages use platinum and platinum-10 percent rhodium as the thermoelectric materials. The thermal resistance layer is silicon monoxide and a protective coating of Al2O3 is deposited on top of the sensor. The

  8. Chambers versus Relaxed Eddy Accumulation: an intercomparison study of two methods for short-term measurements of biogenic CO2 fluxes

    NASA Astrophysics Data System (ADS)

    Jasek, Alina; Zimnoch, Miroslaw; Gorczyca, Zbigniew; Chmura, Lukasz; Necki, Jaroslaw

    2014-05-01

    slight increase towards the city centre. Good agreement between the two measurement methods was obtained, with night-time flux ranging from around 10 to 80 mmol/m2h and day-time net flux reaching -88 mmol/m2h at peak PAR intensity. Positive correlation between the net CO2 flux and intensity of PAR was also observed. Acknowledgements: The study was supported by the Ministry of Science and Higher Education (817.N-COST/2010/0) and the statutory funds of the AGH University of Science and Technology (11.11.220.01).

  9. Growth and properties of transparent conducting CuAlO2 single crystals by a flux self-removal method

    NASA Astrophysics Data System (ADS)

    Yoon, J. S.; Nam, Y. S.; Baek, K. S.; Park, C. W.; Ju, H. L.; Chang, S. K.

    2013-03-01

    We investigated the growth and properties of CuAlO2 single crystals grown by a flux self-removal method. In this method, the flux crept up the wall of an alumina crucible completely during the slow cooling process, leaving flux-free CuAlO2 crystals on the bottom of the crucible. The resulting CuAlO2 crystals had typical dimensions of 0.5-5 mm in the ab-plane and 10-300 μm along the c-axis. The crystals had a hexagonal structure with a=b=2.857(1) Å and c=16.939(2) Å. Their resistivity was anisotropic with a c-axis resistivity (ρc) about ˜17 times higher than the ab-plane resistivity (ρab). However, both ρab and ρc showed thermally activated behavior with the same activation energy of ˜0.6 eV. The CuAlO2 crystals had direct and indirect bandgaps of 3.40 eV and 2.22 eV, respectively.

  10. Spin dynamics and magnetoelectric coupling mechanism of C o4N b2O9

    NASA Astrophysics Data System (ADS)

    Deng, Guochu; Cao, Yiming; Ren, Wei; Cao, Shixun; Studer, Andrew J.; Gauthier, Nicolas; Kenzelmann, Michel; Davidson, Gene; Rule, Kirrily C.; Gardner, Jason S.; Imperia, Paolo; Ulrich, Clemens; McIntyre, Garry J.

    2018-02-01

    Neutron powder diffraction experiments reveal that C o4N b2O9 forms a noncollinear in-plane magnetic structure with C o2 + moments lying in the a b plane. The spin-wave excitations of this magnet were measured by using inelastic neutron scattering and soundly simulated by a dynamic model involving nearest- and next-nearest-neighbor exchange interactions, in-plane anisotropy, and the Dzyaloshinskii-Moriya interaction. The in-plane magnetic structure of C o4N b2O9 is attributed to the large in-plane anisotropy, while the noncollinearity of the spin configuration is attributed to the Dzyaloshinskii-Moriya interaction. The high magnetoelectric coupling effect of C o4N b2O9 in fields can be explained by its special in-plane magnetic structure.

  11. Expansion of antimonato polyoxovanadates with transition metal complexes: (Co(N3C5H15)2)2[{Co(N3C5H15)2}V15Sb6O42(H2O)]·5H2O and (Ni(N3C5H15)2)2[{Ni(N3C5H15)2}V15Sb6O42(H2O)]·8H2O.

    PubMed

    Antonova, Elena; Näther, Christian; Kögerler, Paul; Bensch, Wolfgang

    2012-02-20

    Two new polyoxovanadates (Co(N(3)C(5)H(15))(2))(2)[{Co(N(3)C(5)H(15))(2)}V(15)Sb(6)O(42)(H(2)O)]·5H(2)O (1) and (Ni(N(3)C(5)H(15))(2))(2)[{Ni(N(3)C(5)H(15))(2)}V(15)Sb(6)O(42)(H(2)O)]·8H(2)O (2) (N(3)C(5)H(15) = N-(2-aminoethyl)-1,3-propanediamine) were synthesized under solvothermal conditions and structurally characterized. In both structures the [V(15)Sb(6)O(42)(H(2)O)](6-) shell displays the main structural motif, which is strongly related to the {V(18)O(42)} archetype cluster. Both compounds crystallize in the triclinic space group P1 with a = 14.3438(4), b = 16.6471(6), c = 18.9186(6) Å, α = 87.291(3)°, β = 83.340(3)°, γ = 78.890(3)°, and V = 4401.4(2) Å(3) (1) and a = 14.5697(13), b = 15.8523(16), c = 20.2411(18) Å, α = 86.702(11)°, β = 84.957(11)°, γ = 76.941(11)°, and V = 4533.0(7) Å(3) (2). In the structure of 1 the [V(15)Sb(6)O(42)(H(2)O)](6-) cluster anion is bound to a [Co(N(3)C(5)H(15))(2)](2+) complex via a terminal oxygen atom. In the Co(2+)-centered complex, one of the amine ligands coordinates in tridentate mode and the second one in bidentate mode to form a strongly distorted CoN(5)O octahedron. Similarly, in compound 2 an analogous NiN(5)O complex is joined to the [V(15)Sb(6)O(42)(H(2)O)](6-) anion via the same attachment mode. A remarkable difference between the two compounds is the orientation of the noncoordinated propylamine group leading to intermolecular Sb···O contacts in 1 and to Sb···N interactions in 2. In the solid-state lattices of 1 and 2, two additional [M(N(3)C(5)H(15))(2)](2+) complexes act as countercations and are located between the [{M(N(3)C(5)H(15))(2)}V(15)Sb(6)O(42)(H(2)O)](4-) anions. Between the anions and cations strong N-H···O hydrogen bonds are observed. In both compounds the clusters are stacked along the b axis in an ABAB fashion with cations and water molecules occupying the space between the clusters. Magnetic characterization demonstrates that the Ni(2+) and Co(2+) cations do not

  12. A new frontier in CO2 flux measurements using a highly portable DIAL laser system

    PubMed Central

    Queiβer, Manuel; Granieri, Domenico; Burton, Mike

    2016-01-01

    Volcanic CO2 emissions play a key role in the geological carbon cycle, and monitoring of volcanic CO2 fluxes helps to forecast eruptions. The quantification of CO2 fluxes is challenging due to rapid dilution of magmatic CO2 in CO2-rich ambient air and the diffuse nature of many emissions, leading to large uncertainties in the global magmatic CO2 flux inventory. Here, we report measurements using a new DIAL laser remote sensing system for volcanic CO2 (CO2DIAL). Two sites in the volcanic zone of Campi Flegrei (Italy) were scanned, yielding CO2 path-amount profiles used to compute fluxes. Our results reveal a relatively high CO2 flux from Campi Flegrei, consistent with an increasing trend. Unlike previous methods, the CO2DIAL is able to measure integrated CO2 path-amounts at distances up to 2000 m using virtually any solid surface as a reflector, whilst also being highly portable. This opens a new frontier in quantification of geological and anthropogenic CO2 fluxes. PMID:27652775

  13. Impact of the heatwave in 2003 on the summer CH4 and N2O budget of a spruce forest ecosystem: A four-year comparison

    NASA Astrophysics Data System (ADS)

    Lamers, M.; Fiedler, S.; Jungkunst, H. F.; Stahr, K.; Streck, T.

    2009-04-01

    Both CH4 and N2O reduction and oxidation are highly sensitive to variation in soil moisture. Significant changes of net CH4 and total N2O fluxes from soils can therefore be expected to accompany redistribution for precipitation in the course of climate change where more extreme events are predicted for the future. The extreme summer drought in 2003 offered the unique opportunity to study the impact of such events on the emission of greenhouse gases, such as methane or nitrous oxide, under field conditions. The main objective of the present study was to evaluate the impact of the summer drought in 2003 on the net methane and nitrous oxide budget of a spruce forest ecosystem (South-West Germany) with large variation in soil drainage. During the summers of 2000-2004 we measured net CH4 and N2O fluxes (bi)-weekly using the closed-chamber technique for six different soil types ranging from well-aerated Cambisols to poorly drained Gleysols and a wet Histosol. With regard to CH4 the extreme summer draught (1) did not elevate net CH4-sink function of soils, but (2) highly reduced net CH4-source strength and (3) reversed the net CH4 source of the investigated catchment into a sink. In all four summers investigated, net ecosystem exchange of CH4 was found only in the hydromorphic soils but not in the dominant well-aerated soils. This highlighted the key role of hydromorphic soils for the investigated pedodiverse system. With regard to N2O the summer draught in 2003 significantly reduced N2O emissions at least for the Humic Gleysol and the Sapric Histosol and hence markedly reduced the net N2O source strength of the investigated ecosystem.

  14. Multi-spectra Cosmic Ray Flux Measurement

    NASA Astrophysics Data System (ADS)

    He, Xiaochun; Dayananda, Mathes

    2010-02-01

    The Earth's upper atmosphere is constantly bombarded by rain of charged particles known as primary cosmic rays. These primary cosmic rays will collide with the atmospheric molecules and create extensive secondary particles which shower downward to the surface of the Earth. In recent years, a few studies have been done regarding to the applications of the cosmic ray measurements and the correlations between the Earth's climate conditions and the cosmic ray fluxes [1,2,3]. Most of the particles, which reach to the surface of the Earth, are muons together with a small percentage of electrons, gammas, neutrons, etc. At Georgia State University, multiple cosmic ray particle detectors have been constructed to measure the fluxes and energy distributions of the secondary cosmic ray particles. In this presentation, we will briefly describe these prototype detectors and show the preliminary test results. Reference: [1] K.Borozdin, G.Hogan, C.Morris, W.Priedhorsky, A.Saunders, L.Shultz, M.Teasdale, Nature, Vol.422, 277 (2003). [2] L.V. Egorova, V. Ya Vovk, O.A. Troshichev, Journal of Atmospheric and Terrestrial Physics 62, 955-966 (2000). [3] Henrik Svensmark, Phy. Rev. Lett. 81, 5027 (1998). )

  15. Statistical modeling of the reactions Fe(+) + N2O → FeO(+) + N2 and FeO(+) + CO → Fe(+) + CO2.

    PubMed

    Ushakov, Vladimir G; Troe, Jürgen; Johnson, Ryan S; Guo, Hua; Ard, Shaun G; Melko, Joshua J; Shuman, Nicholas S; Viggiano, Albert A

    2015-08-14

    The rates of the reactions Fe(+) + N2O → FeO(+) + N2 and FeO(+) + CO → Fe(+) + CO2 are modeled by statistical rate theory accounting for energy- and angular momentum-specific rate constants for formation of the primary and secondary cationic adducts and their backward and forward reactions. The reactions are both suggested to proceed on sextet and quartet potential energy surfaces with efficient, but probably not complete, equilibration by spin-inversion of the populations of the sextet and quartet adducts. The influence of spin-inversion on the overall reaction rate is investigated. The differences of the two reaction rates mostly are due to different numbers of entrance states (atom + linear rotor or linear rotor + linear rotor, respectively). The reaction Fe(+) + N2O was studied either with (6)Fe(+) or with (4)Fe(+) reactants. Differences in the rate constants of (6)Fe(+) and (4)Fe(+) reacting with N2O are attributed to different contributions from electronically excited potential energy surfaces, such as they originate from the open-electronic shell reactants.

  16. Theoretical characterization of stable eta1-N2O-, eta2-N2O-, eta1-N2-, and eta2-N2-bound species: intermediates in the addition reactions of nitrogen hydrides with the pentacyanonitrosylferrate(II) ion.

    PubMed

    Olabe, José A; Estiú, Guillermina L

    2003-08-11

    The addition of nitrogen hydrides (hydrazine, hydroxylamine, ammonia, azide) to the pentacyanonitrosylferrate(II) ion has been analyzed by means of density functional calculations, focusing on the identification of stable intermediates along the reaction paths. Initial reversible adduct formation and further decomposition lead to the eta(1)- and eta(2)-linkage isomers of N(2)O and N(2), depending on the nucleophile. The intermediates (adducts and gas-releasing precursors) have been characterized at the B3LYP/6-31G level of theory through the calculation of their structural and spectroscopic properties, modeling the solvent by means of a continuous approach. The eta(2)-N(2)O isomer is formed at an initial stage of adduct decompositions with the hydrazine and azide adducts. Further conversion to the eta(1)-N(2)O isomer is followed by Fe-N(2)O dissociation. Only the eta(1)-N(2)O isomer is predicted for the reaction with hydroxylamine, revealing a kinetically controlled N(2)O formation. eta(1)-N(2) and eta(2)-N(2) isomers are also predicted as stable species.

  17. Reduction and prediction of N2O emission from an Anoxic/Oxic wastewater treatment plant upon DO control and model simulation.

    PubMed

    Sun, Shichang; Bao, Zhiyuan; Li, Ruoyu; Sun, Dezhi; Geng, Haihong; Huang, Xiaofei; Lin, Junhao; Zhang, Peixin; Ma, Rui; Fang, Lin; Zhang, Xianghua; Zhao, Xuxin

    2017-11-01

    In order to make a better understanding of the characteristics of N 2 O emission in A/O wastewater treatment plant, full-scale and pilot-scale experiments were carried out and a back propagation artificial neural network model based on the experimental data was constructed to make a precise prediction of N 2 O emission. Results showed that, N 2 O flux from different units followed a descending order: aerated grit tank>oxic zone≫anoxic zone>final clarifier>primary clarifier, but 99.4% of the total emission of N 2 O (1.60% of N-load) was monitored from the oxic zone due to its big surface area. A proper DO control could reduce N 2 O emission down to 0.21% of N-load in A/O process, and a two-hidden-layers back propagation model with an optimized structure of 4:3:9:1 could achieve a good simulation of N 2 O emission, which provided a new method for the prediction of N 2 O emission during wastewater treatment. Copyright © 2017. Published by Elsevier Ltd.

  18. OH-LIF measurement of H2/O2/N2 flames in a micro flow reactor with a controlled temperature profile

    NASA Astrophysics Data System (ADS)

    Shimizu, T.; Nakamura, H.; Tezuka, T.; Hasegawa, S.; Maruta, K.

    2014-11-01

    This paper presents combustion and ignition characteristic of H2/O2/N2 flames in a micro flow reactor with a controlled temperature profile. OH-LIF measurement was conducted to capture flame images. Flame responses were investigated for variable inlet flow velocity, U, and equivalence ratio, phi. Three kinds of flame responses were experimentally observed for the inlet flow velocities: stable flat flames (normal flames) in the high inlet flow velocity regime; unstable flames called Flames with Repetitive Extinction and Ignition (FREI) in the intermediate flow velocity regime; and stable weak flames in the low flow velocity regime, at phi = 0.6, 1.0 and 1.2. On the other hand, weak flame was not observed at phi = 3.0 by OH-LIF measurement. Computational OH mole fractions showed lower level at the rich conditions than those at stoichiometric and lean conditions. To examine this response of OH signal to equivalence ratio, rate of production analysis was conducted and four kinds of major contributed reaction for OH production: R3(O + H2 <=> H + OH); R38(H + O2 <=> O + OH); R46(H + HO2 <=> 2OH); and R86(2OH <=> O + H2O), were found. Three reactions among them, R3, R38 and R46, did not showed significant difference in rate of OH production for different equivalence ratios. On the other hand, rate of OH production from R86 at phi = 3.0 was extremely lower than those at phi = 0.6 and 1.0. Therefore, R86 was considered to be a key reaction for the reduction of the OH production at phi = 3.0.

  19. Arbuscular mycorrhizal fungi reduce nitrous oxide emissions from N2 O hotspots.

    PubMed

    Storer, Kate; Coggan, Aisha; Ineson, Phil; Hodge, Angela

    2017-12-05

    Nitrous oxide (N 2 O) is a potent, globally important, greenhouse gas, predominantly released from agricultural soils during nitrogen (N) cycling. Arbuscular mycorrhizal fungi (AMF) form a mutualistic symbiosis with two-thirds of land plants, providing phosphorus and/or N in exchange for carbon. As AMF acquire N, it was hypothesized that AMF hyphae may reduce N 2 O production. AMF hyphae were either allowed (AMF) or prevented (nonAMF) access to a compartment containing an organic matter and soil patch in two independent microcosm experiments. Compartment and patch N 2 O production was measured both before and after addition of ammonium and nitrate. In both experiments, N 2 O production decreased when AMF hyphae were present before inorganic N addition. In the presence of AMF hyphae, N 2 O production remained low following ammonium application, but increased in the nonAMF controls. By contrast, negligible N 2 O was produced following nitrate application to either AMF treatment. Thus, the main N 2 O source in this system appeared to be via nitrification, and the production of N 2 O was reduced in the presence of AMF hyphae. It is hypothesized that AMF hyphae may be outcompeting slow-growing nitrifiers for ammonium. This has significant global implications for our understanding of soil N cycling pathways and N 2 O production. © 2017 The Authors. New Phytologist © 2017 New Phytologist Trust.

  20. Airborne Flux Measurements of Volatile Organic Compounds and NOx over a European megacity

    NASA Astrophysics Data System (ADS)

    Shaw, Marvin; Lee, James; Davison, Brian; Misztal, Pawel; Karl, Thomas; Hewitt, Nick; Lewis, Alistair

    2014-05-01

    Ground level ozone (O3) and nitrogen dioxide (NO2) are priority pollutants whose concentrations are closely regulated by European Union Air Quality Directive 2008/50/EC. O3 is a secondary pollutant, produced from a complex chemical interplay between oxides of nitrogen (NOx = NO + NO2) and volatile organic compounds (VOCs). Whilst the basic atmospheric chemistry leading to O3 formation is generally well understood, there are substantial uncertainties associated with the magnitude of emissions of both VOCs and NOx. At present our knowledge of O3 precursor emissions in the UK is primarily derived from National Atmospheric Emission inventories (NAEI) that provide spatially disaggregated estimates at 1x1km resolution, and these are not routinely tested at city or regional scales. Uncertainties in emissions propagate through into uncertainties in predictions of air quality in the future, and hence the likely effectiveness of control policies on both background and peak O3 and NO2 concentrations in the UK. The Ozone Precursor Fluxes in the Urban Environment (OPFUE) project aims to quantify emission rates for NOx and selected VOCs in and around the megacity of London using airborne eddy covariance (AEC). The mathematical foundation for AEC has been extensively reviewed and AEC measurements of ozone, dimethyl sulphide, CO2 and VOCs have been previously reported. During the summer of 2013, approximately 30 hours of airborne flux measurements of toluene, benzene, NO and NO2 were obtained from the NERC Airborne Research and Survey Facility's (ARSF) Dornier-228 aircraft. Over SE England, flights involved repeated south west to north east transects of ~50 km each over Greater London and it's surrounding suburbs and rural areas, flying at the aircraft's minimum operating flight altitude and airspeed (~300m, 80m/s). Mixing ratios of benzene and toluene were acquired at 2Hz using a proton transfer reaction mass spectrometer (PTR-MS) and compared to twice hourly whole air canister