scholarly journals Biogeochemical controls and isotopic signatures of nitrous oxide production by a marine ammonia-oxidizing bacterium

2010 ◽  
Vol 7 (9) ◽  
pp. 2695-2709 ◽  
Author(s):  
C. H. Frame ◽  
K. L. Casciotti

Abstract. Nitrous oxide (N2O) is a trace gas that contributes to the greenhouse effect and stratospheric ozone depletion. The N2O yield from nitrification (moles N2O-N produced per mole ammonium-N consumed) has been used to estimate marine N2O production rates from measured nitrification rates and global estimates of oceanic export production. However, the N2O yield from nitrification is not constant. Previous culture-based measurements indicate that N2O yield increases as oxygen (O2) concentration decreases and as nitrite (NO2−) concentration increases. Here, we have measured yields of N2O from cultures of the marine β-proteobacterium Nitrosomonas marina C-113a as they grew on low-ammonium (50 μM) media. These yields, which were typically between 4 × 10−4 and 7 × 10−4 for cultures with cell densities between 2 × 102 and 2.1 × 104 cells ml−1, were lower than previous reports for ammonia-oxidizing bacteria. The observed impact of O2 concentration on yield was also smaller than previously reported under all conditions except at high starting cell densities (1.5 × 106 cells ml−1), where 160-fold higher yields were observed at 0.5% O2 (5.1 μM dissolved O2) compared with 20% O2 (203 μM dissolved O2). At lower cell densities (2 × 102 and 2.1 × 104 cells ml−1), cultures grown under 0.5% O2 had yields that were only 1.25- to 1.73-fold higher than cultures grown under 20% O2. Thus, previously reported many-fold increases in N2O yield with dropping O2 could be reproduced only at cell densities that far exceeded those of ammonia oxidizers in the ocean. The presence of excess NO2− (up to 1 mM) in the growth medium also increased N2O yields by an average of 70% to 87% depending on O2 concentration. We made stable isotopic measurements on N2O from these cultures to identify the biochemical mechanisms behind variations in N2O yield. Based on measurements of δ15Nbulk, site preference (SP = δ15Nα−δ15Nβ), and δ18O of N2O (δ18O-N2O), we estimate that nitrifier-denitrification produced between 11% and 26% of N2O from cultures grown under 20% O2 and 43% to 87% under 0.5% O2. We also demonstrate that a positive correlation between SP and δ18O-N2O is expected when nitrifying bacteria produce N2O. A positive relationship between SP and δ18O-N2O has been observed in environmental N2O datasets, but until now, explanations for the observation invoked only denitrification. Such interpretations may overestimate the role of heterotrophic denitrification and underestimate the role of ammonia oxidation in environmental N2O production.

2010 ◽  
Vol 7 (2) ◽  
pp. 3019-3059 ◽  
Author(s):  
C. H. Frame ◽  
K. L. Casciotti

Abstract. Nitrous oxide (N2O) is a trace gas that contributes to greenhouse warming of the atmosphere and stratospheric ozone depletion. The N2O yield from nitrification (moles N2O-N produced/mole ammonium-N consumed) has been used to estimate marine N2O production rates from measured nitrification rates and global estimates of oceanic export production. However, the N2O yield from nitrification is not constant. Previous culture-based measurements indicate that N2O yield increases as oxygen (O2) concentration decreases and as nitrite (NO2−) concentration increases. These results were obtained in substrate-rich conditions and may not reflect N2O production in the ocean. Here, we have measured yields of N2O from cultures of the marine β-proteobacterium Nitrosomonas marina C-113a as they grew on low-ammonium (50 μM) media. These yields were lower than previous reports, between 4×10−4 and 7×10−4 (moles N/mole N). The observed impact of O2 concentration on yield was also smaller than previously reported under all conditions except at high starting cell densities (1.5×10


2014 ◽  
Vol 11 (10) ◽  
pp. 2679-2689 ◽  
Author(s):  
T. Yamazaki ◽  
T. Hozuki ◽  
K. Arai ◽  
S. Toyoda ◽  
K. Koba ◽  
...  

Abstract. Nitrous oxide (N2O) is a potent greenhouse gas and produced in denitrification and nitrification by various microorganisms. Site preference (SP) of 15N in N2O, which is defined as the difference in the natural abundance of isotopomers 14N15NO and 15N14NO relative to 14N14NO, has been reported to be a useful tool to quantitatively distinguish N2O production pathways. To determine representative SP values for each microbial process, we firstly measured SP of N2O produced in the enzyme reaction of hydroxylamine oxidoreductase (HAO) purified from two species of ammonia oxidizing bacteria (AOB), Nitrosomonas europaea and Nitrosococcus oceani, and that of nitric oxide reductase (NOR) from Paracoccus denitrificans. The SP value for NOR reaction (−5.9 ± 2.1‰) showed nearly the same value as that reported for N2O produced by P. denitrificans in pure culture. In contrast, SP value for HAO reaction (36.3 ± 2.3‰) was a little higher than the values reported for N2O produced by AOB in aerobic pure culture. Using the SP values obtained by HAO and NOR reactions, we calculated relative contribution of the nitrite (NO2–) reduction (which is followed by NO reduction) to N2O production by N. oceani incubated under different O2 availability. Our calculations revealed that previous in vivo studies might have underestimated the SP value for the NH2OH oxidation pathway possibly due to a small contribution of NO2– reduction pathway. Further evaluation of isotopomer signatures of N2O using common enzymes of other processes related to N2O would improve the isotopomer analysis of N2O in various environments.


2013 ◽  
Vol 10 (10) ◽  
pp. 16615-16643 ◽  
Author(s):  
T. Yamazaki ◽  
T. Hozuki ◽  
K. Arai ◽  
S. Toyoda ◽  
K. Koba ◽  
...  

Abstract. Nitrous oxide (N2O) is a potent greenhouse gas and produced in denitrification and nitrification in environmental nitrogen cycle by various microorganism. Site preference (SP) of 15N in N2O, which is defined as the difference in the natural abundance of isotopomers 14N15NO and 15N14NO relative to 14N14NO, has been reported to be a useful tool to quantitatively distinguish N2O production pathway. To determine representative SP value for each microbial process, we firstly measured SP of N2O produced in the enzyme reaction of hydroxylamine oxidoreductase (HAO) purified from two species of ammonia oxidizing bacteria (AOB), Nitrosomonas europaea and Nitrosococcus oceani, and that of nitric oxide reductase (NOR) from Paracoccus denitrificans, respectively. The SP value for NOR reaction (−5.9 ± 2.1‰) showed nearly the same value as that reported for N2O produced by P. denitrificans in pure culture. In contrast, SP value for HAO reaction (36.3 ± 2.3‰) was a little higher than the values reported for N2O produced by AOB in aerobic pure culture. Using the SP values obtained by HAO and NOR reactions, we calculated relative contribution of the nitrite (NO2–) reduction (which is followed by NO reduction) to N2O production by N. oceani incubated under different O2 availability. Our calculations revealed that previous in vivo studies might have underestimated the SP value for NH2OH oxidation pathway possibly due to a small contribution of NO2– reduction pathway. Further evaluation of isotopomer signatures of N2O using common enzymes of other processes related to N2O would improve the isotopomer analysis of N2O in various environments.


2017 ◽  
Vol 17 (43) ◽  
pp. 23-27
Author(s):  
Tumendelger A ◽  
Byambadorj T ◽  
C Bors ◽  
A Lorke

Nitrous oxide (N2O) is an increasing greenhouse gas in the troposphere and a potential destroyer of stratospheric ozone layer. Wastewater treatment plant (WWTP) is one of the anthropogenic N2O sources because inorganic and organic nitrogen compounds are converted to nitrate (NO3-, in the case of standard system) or N2 (in the case of advanced system) by bacterial nitrification and denitrifcation processes in WWTP. These major processes can be distinguished by isotopocule analysis. In order to reveal production mechanisms of N2O in a standard wastewater treatment, we made water sampling at the central WWTP in Ulaanbaatar. The water samples collected from seven stations including biological reaction tanks were measured for concentration and isotopocule ratios of dissolved N2O and other inorganic nitrogen. Dissolved N2O concentration was extremely higher than that expected under atmospheric equilibrium (about 9 nmol/l) at all stations, indicating that this system is a potential source of N2O. It showed a gradual increase with the progress of biological reaction and the highest concentration (335.7 nmol/l) was observed at station N5-4 of the aeration tank when the DO was 5.7 mg/l. Nitrification by nitrifying bacteria could actively occur by the concentration of NH4+ decreased whereas NO2- and NO3- showed a temporal and monotonic increase, respectively, under high DO concentration. Although the reported values of site preference (SP) of N2O, the difference in 15N/14N ratio between central (α) and terminal (β) nitrogen, produced via NO2- reduction (SP(ND)), including both nitrifier and denitrifier denitrification, and NH2OH oxidation (SP(HO)) ranged from -10.7‰ to 0‰ and 31.4‰ to 36.3‰, respectively, the observed SP at aeration tank was close to SP(ND) rather than SP(HO). It was ranged from 0.4‰ to 13.3‰ when N2O concentration was high, implying that the NO2- reduction made a greater contribution to N2O production. Slightly elevated SP (13.3‰) only at station N5-1 was derived from the mixing of N2O produced via NH2OH oxidation and the maximal contribution of this pathway was estimated to be about 40%. In other words, the contribution of NO2- reduction was more than 60%.


2011 ◽  
Vol 39 (6) ◽  
pp. 1832-1837 ◽  
Author(s):  
Kartik Chandran ◽  
Lisa Y. Stein ◽  
Martin G. Klotz ◽  
Mark C.M. van Loosdrecht

Chemolithoautotrophic AOB (ammonia-oxidizing bacteria) form a crucial component in microbial nitrogen cycling in both natural and engineered systems. Under specific conditions, including transitions from anoxic to oxic conditions and/or excessive ammonia loading, and the presence of high nitrite (NO2−) concentrations, these bacteria are also documented to produce nitric oxide (NO) and nitrous oxide (N2O) gases. Essentially, ammonia oxidation in the presence of non-limiting substrate concentrations (ammonia and O2) is associated with N2O production. An exceptional scenario that leads to such conditions is the periodical switch between anoxic and oxic conditions, which is rather common in engineered nitrogen-removal systems. In particular, the recovery from, rather than imposition of, anoxic conditions has been demonstrated to result in N2O production. However, applied engineering perspectives, so far, have largely ignored the contribution of nitrification to N2O emissions in greenhouse gas inventories from wastewater-treatment plants. Recent field-scale measurements have revealed that nitrification-related N2O emissions are generally far higher than emissions assigned to heterotrophic denitrification. In the present paper, the metabolic pathways, which could potentially contribute to NO and N2O production by AOB have been conceptually reconstructed under conditions especially relevant to engineered nitrogen-removal systems. Taken together, the reconstructed pathways, field- and laboratory-scale results suggest that engineering designs that achieve low effluent aqueous nitrogen concentrations also minimize gaseous nitrogen emissions.


2016 ◽  
Vol 75 (3) ◽  
pp. 491-500 ◽  
Author(s):  
Longqi Lang ◽  
Mathieu Pocquet ◽  
Bing-Jie Ni ◽  
Zhiguo Yuan ◽  
Mathieu Spérandio

The aim of this work is to compare the capability of two recently proposed two-pathway models for predicting nitrous oxide (N2O) production by ammonia-oxidizing bacteria (AOB) for varying ranges of dissolved oxygen (DO) and nitrite. The first model includes the electron carriers whereas the second model is based on direct coupling of electron donors and acceptors. Simulations are confronted to extensive sets of experiments (43 batches) from different studies with three different microbial systems. Despite their different mathematical structures, both models could well and similarly describe the combined effect of DO and nitrite on N2O production rate and emission factor. The model-predicted contributions for nitrifier denitrification pathway and hydroxylamine pathway also matched well with the available isotopic measurements. Based on sensitivity analysis, calibration procedures are described and discussed for facilitating the future use of those models.


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.


2020 ◽  
Vol 20 (11) ◽  
pp. 6495-6519 ◽  
Author(s):  
Longfei Yu ◽  
Eliza Harris ◽  
Stephan Henne ◽  
Sarah Eggleston ◽  
Martin Steinbacher ◽  
...  

Abstract. Atmospheric nitrous oxide (N2O) levels have been continuously growing since preindustrial times. Mitigation requires information about sources and sinks on the regional and global scales. Isotopic composition of N2O in the atmosphere could contribute valuable constraints. However, isotopic records of N2O in the unpolluted atmosphere remain too scarce for large-scale N2O models. Here, we report the results of discrete air samples collected weekly to biweekly over a 5-year period at the high-altitude research station Jungfraujoch, located in central Switzerland. High-precision N2O isotopic measurements were made using a recently developed preconcentration and laser spectroscopy technique. The measurements of discrete samples were accompanied by in situ continuous measurements of N2O mixing ratios. Our results indicate a pronounced seasonal pattern with minimum N2O mixing ratios in late summer, associated with a maximum in δ15Nbulk and a minimum in intramolecular 15N site preference (δ15NSP). This pattern is most likely due to stratosphere–troposphere exchange (STE), which delivers N2O-depleted but 15N-enriched air from the stratosphere into the troposphere. Variability in δ15NSP induced by changes in STE may be masked by biogeochemical N2O production processes in late summer, which are possibly dominated by a low-δ15NSP pathway of N2O production (denitrification), providing an explanation for the observed seasonality of δ15NSP. Footprint analyses and atmospheric transport simulations of N2O for Jungfraujoch suggest that regional emissions from the planetary boundary layer contribute to seasonal variations of atmospheric N2O isotopic composition at Jungfraujoch, albeit more clearly for δ15NSP and δ18O than for δ15Nbulk. With the time series of 5 years, we obtained a significant interannual trend for δ15Nbulk after deseasonalization (-0.052±0.012 ‰ a−1), indicating that the atmospheric N2O increase is due to isotopically depleted N2O sources. We estimated the average isotopic signature of anthropogenic N2O sources with a two-box model to be -8.6±0.6 ‰ for δ15Nbulk, 34.8±3 ‰ for δ18O and 10.7±4 ‰ for δ15NSP. Our study demonstrates that seasonal variation of N2O isotopic composition in the background atmosphere is important when determining interannual trends. More frequent, high-precision and interlaboratory-compatible measurements of atmospheric N2O isotopocules, especially for δ15NSP, are needed to better constrain anthropogenic N2O sources and thus the contribution of biogeochemical processes to N2O growth on the global scale.


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.


Geobiology ◽  
2011 ◽  
Vol 9 (6) ◽  
pp. 471-480 ◽  
Author(s):  
B. P. HEDLUND ◽  
A. I. MCDONALD ◽  
J. LAM ◽  
J. A. DODSWORTH ◽  
J. R. BROWN ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document