scholarly journals Natural Nitrogen Isotope Ratios as a Potential Indicator of N2O Production Pathways in a Floodplain Fen

Water ◽  
2020 ◽  
Vol 12 (2) ◽  
pp. 409
Author(s):  
Mohit Masta ◽  
Holar Sepp ◽  
Jaan Pärn ◽  
Kalle Kirsimäe ◽  
Ülo Mander

Nitrous oxide (N2O), a major greenhouse gas and ozone depleter, is emitted from drained organic soils typically developed in floodplains. We investigated the effect of the water table depth and soil oxygen (O2) content on N2O fluxes and their nitrogen isotope composition in a drained floodplain fen in Estonia. Measurements were done at natural water table depth, and we created a temporary anoxic environment by experimental flooding. From the suboxic peat (0.5–6 mg O2/L) N2O emissions peaked at 6 mg O2/L and afterwards decreased with decreasing O2. From the anoxic and oxic peat (0 and >6 mg O2/L, respectively) N2O emissions were low. Under anoxic conditions the δ15N/δ14N ratio of the top 10 cm peat layer was low, gradually decreasing to 30 cm. In the suboxic peat, δ15N/δ14N ratios increased with depth. In samples of peat fluctuating between suboxic and anoxic, the elevated 15N/14N ratios (δ15N = 7–9‰ ambient N2) indicated intensive microbial processing of nitrogen. Low values of site preference (SP; difference between the central and peripheral 15N atoms) and δ18O-N2O in the captured gas samples indicate nitrifier denitrification in the floodplain fen.

2019 ◽  
Author(s):  
Guillaume Humbert ◽  
Mathieu Sébilo ◽  
Justine Fiat ◽  
Longqi Lang ◽  
Ahlem Filali ◽  
...  

Abstract. Nitrous oxide (N2O) emissions by a nitrifying biofilm reactor were investigated with N2O isotopocules. The site preference of N2O (15N-SP) indicated the contribution of producing and consuming pathways in response to changes in oxygenation level (from 0 to 21 % O2 in the gas mix), temperature (from 13.5 to 22.3 °C), and ammonium concentrations (from 6.2 to 62.1 mg N L−1). Nitrite reduction, either nitrifier-denitrification or heterotrophic denitrification, was the main N2O producing pathway under the tested conditions. Nitrite oxidation rates decreased as compared to ammonium oxidation rates at temperatures above 20 °C and sub-optimal oxygen levels, increasing N2O production by the nitrite reduction pathway. Below 20 °C, a difference in temperature sensitivity between hydroxylamine and ammonium oxidation rates is most likely responsible for an increase in the N2O production via the hydroxylamine oxidation pathway (nitrification). A negative correlation between the reaction kinetics and the apparent isotope fractionation was additionally shown from the variations of δ15N and δ18O values of N2O produced from ammonium.


2020 ◽  
Vol 17 (4) ◽  
pp. 979-993
Author(s):  
Guillaume Humbert ◽  
Mathieu Sébilo ◽  
Justine Fiat ◽  
Longqi Lang ◽  
Ahlem Filali ◽  
...  

Abstract. Nitrous oxide (N2O) emissions from a nitrifying biofilm reactor were investigated with N2O isotopocules. The nitrogen isotopomer site preference of N2O (15N-SP) indicated the contribution of producing and consuming pathways in response to changes in oxygenation level (from 0 % to 21 % O2 in the gas mix), temperature (from 13.5 to 22.3 ∘C) and ammonium concentrations (from 6.2 to 62.1 mg N L−1). Nitrite reduction, either nitrifier denitrification or heterotrophic denitrification, was the main N2O-producing pathway under the tested conditions. Difference between oxidative and reductive rates of nitrite consumption was discussed in relation to NO2- concentrations and N2O emissions. Hence, nitrite oxidation rates seem to decrease as compared to ammonium oxidation rates at temperatures above 20 ∘C and under oxygen-depleted atmosphere, increasing N2O production by the nitrite reduction pathway. Below 20 ∘C, a difference in temperature sensitivity between hydroxylamine and ammonium oxidation rates is most likely responsible for an increase in N2O production via the hydroxylamine oxidation pathway (nitrification). A negative correlation between the reaction kinetics and the apparent isotope fractionation was additionally shown from the variations of δ15N and δ18O values of N2O produced from ammonium. The approach and results obtained here, for a nitrifying biofilm reactor under variable environmental conditions, should allow for application and extrapolation of N2O emissions from other systems such as lakes, soils and sediments.


2019 ◽  
Vol 16 (23) ◽  
pp. 4555-4575 ◽  
Author(s):  
Arezoo Taghizadeh-Toosi ◽  
Lars Elsgaard ◽  
Tim J. Clough ◽  
Rodrigo Labouriau ◽  
Vibeke Ernstsen ◽  
...  

Abstract. Organic soils drained for crop production or grazing land are agroecosystems with potentially high but variable emissions of nitrous oxide (N2O). The present study investigated the regulation of N2O emissions in a raised bog area drained for agriculture, which is classified as potentially acid sulfate soil. We hypothesised that pyrite (FeS2) oxidation was a potential driver of N2O emissions through microbially mediated reduction of nitrate (NO3-). Two sites with rotational grass, and two sites with a potato crop, were equipped for monitoring of N2O emissions and soil N2O concentrations at the 5, 10, 20, 50 and 100 cm depth during weekly field campaigns in spring and autumn 2015. Further data acquisition included temperature, precipitation, soil moisture, water table (WT) depth, and soil NO3- and ammonium (NH4+) concentrations. At all sites, the soil was acidic, with pH ranging from 4.7 to 5.4. Spring and autumn monitoring periods together represented between 152 and 174 d, with cumulative emissions of 4–5 kg N2O-N ha−1 at sites with rotational grass and 20–50 kg N2O-N ha−1 at sites with a potato crop. Equivalent soil gas-phase concentrations of N2O at grassland sites varied between 0 and 25 µL L−1 except for a sampling after slurry application at one of the sites in spring, with a maximum of 560 µL L−1 at the 1 m depth. At the two potato sites the levels of below-ground N2O concentrations ranged from 0.4 to 2270 µL L−1 and from 0.1 to 470 µL L−1, in accordance with the higher soil mineral N availability at arable sites. Statistical analyses using graphical models showed that soil N2O concentration in the capillary fringe (i.e. the soil volume above the water table influenced by tension saturation) was the strongest predictor of N2O emissions in spring and, for grassland sites, also in the autumn. For potato sites in autumn, there was evidence that NO3- availability in the topsoil and temperature were the main controls on N2O emissions. Chemical analyses of intact soil cores from the 0 to 1 m depth, collected at adjacent grassland and potato sites, showed that the total reduction capacity of the peat soil (assessed by cerium(IV) reduction) was much higher than that represented by FeS2, and the concentrations of total reactive iron (TRFe) were higher than those of FeS2. Based on the statistical graphical models and the tentative estimates of reduction capacities, FeS2 oxidation was unlikely to be important for N2O emissions. Instead, archaeal ammonia oxidation and either chemodenitrification or nitrifier denitrification were considered to be plausible pathways of N2O production in spring, whereas in the autumn heterotrophic denitrification may have been more important at arable sites.


SOIL ◽  
2019 ◽  
Vol 5 (2) ◽  
pp. 265-274 ◽  
Author(s):  
Katelyn A. Congreves ◽  
Trang Phan ◽  
Richard E. Farrell

Abstract. Understanding the production pathways of potent greenhouse gases, such as nitrous oxide (N2O), is essential for accurate flux prediction and for developing effective adaptation and mitigation strategies in response to climate change. Yet there remain surprising gaps in our understanding and precise quantification of the underlying production pathways – such as the relationship between soil moisture and N2O production pathways. A powerful, but arguably underutilized, approach for quantifying the relative contribution of nitrification and denitrification to N2O production involves determining 15N2O isotopomers and 15N site preference (SP) via spectroscopic techniques. Using one such technique, we conducted a short-term incubation where N2O production and 15N2O isotopomers were measured 24 h after soil moisture treatments of 40 % to 105 % water-filled pore space (WFPS) were established for each of three soils that differed in nutrient levels, organic matter, and texture. Relatively low N2O fluxes and high SP values indicted nitrification during dry soil conditions, whereas at higher soil moisture, peak N2O emissions coincided with a sharp decline in SP, indicating denitrification. This pattern supports the classic N2O production curves from nitrification and denitrification as inferred by earlier research; however, our isotopomer data enabled the quantification of source partitioning for either pathway. At soil moisture levels < 53 % WFPS, the fraction of N2O attributed to nitrification (FN) predominated but thereafter decreased rapidly with increasing soil moisture (x), according to FN=3.19-0.041x, until a WFPS of 78 % was reached. Simultaneously, from WFPS of 53 % to 78 %, the fraction of N2O that was attributed to denitrification (FD) was modelled as FD=-2.19+0.041x; at moisture levels of > 78 %, denitrification completely dominated. Clearly, the soil moisture level during transition is a key regulator of N2O production pathways. The presented equations may be helpful for other researchers in estimating N2O source partitioning when soil moisture falls within the transition from nitrification to denitrification.


2019 ◽  
Author(s):  
Kate A. Congreves ◽  
Trang Phan ◽  
Richard E. Farrell

Abstract. Understanding the production pathways of potent greenhouse gases, such as nitrous oxide (N2O), is essential for accurate flux prediction and for developing effective adaptation and mitigation strategies in response to climate change. Yet, there remain surprising gaps in our understanding and precise quantification of the underlying production pathways – such as the relationship between soil moisture and N2O production pathways. A powerful, but arguably underutilized, approach for quantifying the relative contribution of nitrification and denitrification to N2O production involves determining 15N2O isotopomers and 15N site preference (SP) via spectroscopic techniques. Using one such technique we conducted a short-term incubation to precisely quantify the relationship between soil moisture and N2O production pathways. For each of three soils, microcosms were arranged in a complete random design with four replicates; each microcosm consisted of air-dried soil packed into plastic petri dishes wherein moisture treatments were established for water contents equivalent to 45 to 105 % water-filled pore space (WFPS). The microcosms were placed in 1-L jars and sealed; headspace samples were collected after 24-h and analyzed for total N2O concentrations using gas chromatography, and for 15N2O isotopomers using cavity ring-down spectroscopy. Relatively low N2O fluxes and high SP values indicted nitrification during dry soil conditions, whereas at higher soil moisture, peak N2O emissions coincided with a sharp decline in SP indicating denitrification. This pattern supports the classic N2O production curves from nitrification and denitrification as inferred by earlier research; however, our isotopomer data enabled the quantification of source partitioning for either pathway thereby providing clarity on N2O sources during the transition from nitrification to denitrification. At soil moisture levels  78 %, denitrification completely dominated. Clearly, the soil moisture levels during transition is a key regulation of N2O production pathways.


10.29007/w6rq ◽  
2018 ◽  
Author(s):  
Theoni Massara ◽  
Borja Solis Duran ◽  
Albert Guisasola ◽  
Evina Katsou ◽  
Juan Antonio Baeza

Nitrous oxide (N2O), a greenhouse gas with a significant global warming potential, can be produced during the biological nutrient removal in wastewater treatment plants (WWTPs). N2O modelling under dynamic conditions is of vital importance for its mitigation. Following the activated sludge models (ASM) layout, an ASM-type model was developed considering three biological N2O production pathways for a municipal anaerobic/anoxic/aerobic (A2/O) WWTP performing chemical oxygen demand, nitrogen and phosphorus removal. Precisely, the N2O production pathways included were: nitrifier denitrification, hydroxylamine oxidation, and heterotrophic denitrification, with the first two linked to the ammonia oxidizing bacteria (AOB) activity. A stripping effectivity (SE) factor was used to mark the non-ideality of the stripping modelling. With the dissolved oxygen (DO) in the aerobic compartment ranging from 1.8 to 2.5 mg L-1, partial nitrification and high N2O production via nitrifier denitrification occurred. Therefore, low aeration strategies can effectively lead to a low overall carbon footprint only if complete nitrification is guaranteed. After suddenly increasing the influent ammonium load, the AOB had a greater growth compared to the NOB. N2O hotspot was again nitrifier denitrification. Especially under concurring partial nitrification and high stripping (i.e. combination of low DO and high SEs), the highest N2O emission factors were noted.


2007 ◽  
Vol 4 (5) ◽  
pp. 729-741 ◽  
Author(s):  
J. Charpentier ◽  
L. Farias ◽  
N. Yoshida ◽  
N. Boontanon ◽  
P. Raimbault

Abstract. The mechanisms of microbial nitrous oxide (N2O) production in the ocean have been the subject of many discussions in recent years. New isotopomeric tools can further refine our knowledge of N2O sources in natural environments. This study compares hydrographic, N2O concentration, and N2O isotopic and isotopomeric data from three stations along a coast-perpendicular transect in the South Pacific Ocean, extending from the center (Sts. GYR and EGY) of the subtropical oligotrophic gyre (~26° S; 114° W) to the upwelling zone (St. UPX) off the central Chilean coast (~34° S). Although AOU/N2O and NO3− trends support the idea that most of the N2O (mainly from intermediate water (200–600 m)) comes from nitrification, N2O isotopomeric composition (intramolecular distribution of 15N isotopes) expressed as SP (site preference of 15N) shows low values (10 to 12\\permil) that could be attributed to the production through of microbial nitrifier denitrification (reduction of nitrite to N2O mediated by ammonium oxidizers). The coincidence of this SP signal with high – stability layer, where sinking organic particles can accumulate, suggests that N2O could be produced by nitrifier denitrification inside particles. It is postulated that deceleration of particles in the pycnocline can modify the advection - diffusion balance inside particles, allowing the accumulation of nitrite and O2 depletion suitable for nitrifier denitrication. As lateral advection seems to be relatively insignificant in the gyre, in situ nitrifier denitrification could account for 40–50% of the N2O produced in this layer. In contrast, coastal upwelling system is characterized by O2 deficient condition and some N deficit in a eutrophic system. Here, N2O accumulates up to 480% saturation, and isotopic and isotopomer signals show highly complex N2O production processes, which presumably reflect both the effect of nitrification and denitrification at low O2 levels on N2O production, but net N2O consumption by denitrification was not observed.


2017 ◽  
Author(s):  
Joshua A. Haslun ◽  
Nathaniel E. Ostrom ◽  
Eric L. Hegg ◽  
Peggy H. Ostrom

Abstract. Soil microbial processes, stimulated by agricultural fertilization, account for 90 % of anthropogenic nitrous oxide (N2O), the leading source of ozone depletion and a potent greenhouse gas. Efforts to reduce N2O flux commonly focus on reducing fertilization rates. Management of microbial processes responsible for N2O production may also be used to reduce N2O emissions, but this requires knowledge of the prevailing process. To this end, stable isotopes of N2O have been applied to differentiate N2O produced by nitrification and denitrification. To better understand the factors contributing to isotopic variation during denitrification, we characterized the δ15N, δ18O and site preference (SP; the intramolecular distribution of 15N in N2O) of N2O produced during NO3− reduction by Pseudomonas chlororaphis subsp. aureofaciens and P. c. subsp. chlororaphis. In addition to species, treatments included electron donor (citrate and succinate) and electron donor concentration (0.01 mM, 0.1 mM, 1 mM, and 10 mM) as factors. In contrast to the expectation of a Rayleigh model, all treatments exhibited curvilinear behaviour between δ15N or δ18O and [−flnf/(1−f)]. The curvilinear behaviour indicates that the fractionation factor changed over the course of the reaction, something that is not unexpected for a multi-step process such as denitrification. Using the derivative of the equation, we estimated that the net isotope effects (η) vary by as much as 100 ‰ over the course of a single reaction, placing challenges for using δ15N and δ18O as apportionment tools. In contrast, SP for denitrification was not affected by the extent of the reaction, the electron donor source, or concentration, although the mean SP of N2O produced by each species differed. Therefore, SP remains a robust indicator of the origin of N2O. To improve apportionment estimates with SP, future studies could evaluate other factors that contribute to the variation in SP.


2014 ◽  
Vol 18 (9) ◽  
pp. 3319-3339 ◽  
Author(s):  
M. Bechtold ◽  
B. Tiemeyer ◽  
A. Laggner ◽  
T. Leppelt ◽  
E. Frahm ◽  
...  

Abstract. Fluxes of the three main greenhouse gases (GHG) CO2, CH4 and N2O from peat and other soils with high organic carbon contents are strongly controlled by water table depth. Information about the spatial distribution of water level is thus a crucial input parameter when upscaling GHG emissions to large scales. Here, we investigate the potential of statistical modeling for the regionalization of water levels in organic soils when data covers only a small fraction of the peatlands of the final map. Our study area is Germany. Phreatic water level data from 53 peatlands in Germany were compiled in a new data set comprising 1094 dip wells and 7155 years of data. For each dip well, numerous possible predictor variables were determined using nationally available data sources, which included information about land cover, ditch network, protected areas, topography, peatland characteristics and climatic boundary conditions. We applied boosted regression trees to identify dependencies between predictor variables and dip-well-specific long-term annual mean water level (WL) as well as a transformed form (WLt). The latter was obtained by assuming a hypothetical GHG transfer function and is linearly related to GHG emissions. Our results demonstrate that model calibration on WLt is superior. It increases the explained variance of the water level in the sensitive range for GHG emissions and avoids model bias in subsequent GHG upscaling. The final model explained 45% of WLt variance and was built on nine predictor variables that are based on information about land cover, peatland characteristics, drainage network, topography and climatic boundary conditions. Their individual effects on WLt and the observed parameter interactions provide insight into natural and anthropogenic boundary conditions that control water levels in organic soils. Our study also demonstrates that a large fraction of the observed WLt variance cannot be explained by nationally available predictor variables and that predictors with stronger WLt indication, relying, for example, on detailed water management maps and remote sensing products, are needed to substantially improve model predictive performance.


2018 ◽  
Vol 15 (12) ◽  
pp. 3873-3882 ◽  
Author(s):  
Joshua A. Haslun ◽  
Nathaniel E. Ostrom ◽  
Eric L. Hegg ◽  
Peggy H. Ostrom

Abstract. Soil microbial processes, stimulated by agricultural fertilization, account for 90 % of anthropogenic nitrous oxide (N2O), the leading source of ozone depletion and a potent greenhouse gas. Efforts to reduce N2O flux commonly focus on reducing fertilization rates. Management of microbial processes responsible for N2O production may also be used to reduce N2O emissions, but this requires knowledge of the prevailing process. To this end, stable isotopes of N2O have been applied to differentiate N2O produced by nitrification and denitrification. To better understand the factors contributing to isotopic variation during denitrification, we characterized the δ15N, δ18O and site preference (SP; the intramolecular distribution of 15N in N2O) of N2O produced during NO3- reduction by Pseudomonas chlororaphis subsp. aureofaciens and P. c. subsp. chlororaphis. The terminal product of denitrification for these two species is N2O because they lack the gene nitrous oxide reductase, which is responsible for the reduction of N2O to N2. In addition to species, treatments included electron donor (citrate and succinate) and electron donor concentration (0.01, 0.1, 1 and 10 mM) as factors. In contrast to the expectation of a Rayleigh model, all treatments exhibited curvilinear behaviour between δ15N or δ18O and the extent of the reaction. The curvilinear behaviour indicates that the fractionation factor changed over the course of the reaction, something that is not unexpected for a multi-step process such as denitrification. Using the derivative of the equation, we estimated that the net isotope effects (η) vary by as much as 100 ‰ over the course of a single reaction, presenting challenges for using δ15N and δ18O as apportionment tools. In contrast, SP for denitrification was not affected by the extent of the reaction, the electron donor source or concentration, although the mean SP of N2O produced by each species differed. Therefore, SP remains a robust indicator of the origin of N2O. To improve apportionment estimates with SP, future studies could evaluate other factors that contribute to the variation in SP.


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