Impacts of grazing intensity on denitrification and N<Subscript>2</Subscript>O production in a semi-arid grassland ecosystem

N₂O production from denitrification in soils contributes to the enhanced greenhouse effect and the destruction of the stratospheric ozone. Ungulate grazing affects denitrification and the production of N₂O. The short-term effect of grazing on denitrification and N₂O production has been examined in several grassland ecosystems. However, the effects of long-term grazing have rarely been studied. We measured denitrification and N₂O production during the 2005 and 2006 growing seasons in a long-term (17 years) experiment that had five grazing intensities (GI; 0.00, 1.33, 2.67, 4.00 and 5.33 sheep ha⁻¹). We found that denitrification and N₂O production rates were seasonally variable during the measurement period, with higher values observed in summer and lower values found in spring and autumn. The grazed treatments resulted in decreased denitrification and N₂O production, primarily due to the reduced soil nitrate concentration and organic N content under the long-term grazing. This supported our hypothesis that long-term over-grazing suppresses denitrification and N₂O production. Although significant differences in denitrification and N₂O production were not found between the four GI, there was a general trend that cumulative denitrification and N₂O production decreased as grazing intensity increased, especially in 2006. Lower N losses via denitrification and N₂O production in the grazed plots, to some extent, may contribute to the mitigation of greenhouse gas emission and help to preserve soil N and ameliorate the negative impacts of grazing on plant growth, productivity, and ecological restoration processes in the temperate steppe in northern China.     

Net sediment N2 fluxes in a southern New England estuary: variations in space and time

Over the past three decades, Narragansett Bay has undergone various ecological changes, including significant decreases in water column chlorophyll a concentrations, benthic oxygen uptake, and benthic nutrient regeneration rates. To add to this portrait of change, we measured the net flux of N₂ across the sediment–water interface over an annual cycle using the N₂/Ar technique at seven sites in the bay for comparison with measurements made decades ago. Net denitrification rates ranged from about 10–90 μmol N₂–N m^?2 h^?1 over the year. Denitrification rates were not significantly different among sites and had no clear correlation with temperature. Net nitrogen fixation (?5 to ?650 μmol N₂–N m^?2 h^?1) was measured at three sites and only observed in summer (June–August). Neither denitrification nor nitrogen fixation exhibited a consistent relationship with sediment oxygen demand or with fluxes of nitrite, nitrate, ammonium, total dissolved inorganic nitrogen, or dissolved inorganic phosphate across all stations. In contrast to the mid-bay historical site where denitrification rates have declined, denitrification rates in the Providence River Estuary have not changed significantly over the past 30 years.     

Measurement of denitrification in rivers: an integrated, whole reach approach

Rivers are believed to play an important role in nitrogen removal via denitrification. Unfortunately, there are few data quantifying these processes in situ, primarily due to methodological constraints. We have developed a new approach for estimating denitrification in rivers at the whole reach scale and have applied this approach to three small rivers, the Millstone River in central New Jersey, and the Iroquois River and Sugar Creek in northwest Indiana–northeast Illinois (USA). The approach is based on measuring the change in dissolved N₂ concentration as a parcel of water moves downstream. Two volatile, non-reactive tracers (propane and isobutane) were co-injected, and the rate of change in the ratio of these gases was used to calculate a first-order transfer rate of N₂ (K_N2) to correct for loss of the gas to the atmosphere. Nitrogen removal via denitrification ranged between 0.27 ± 1.21 mmol N m^–2 h^–1 in Sugar Creek during May 2000 and 15.81 ± 2.51 mmol N m^–2 h^–1 in the Millstone River during March 2001. This approach could permit testing of factors that are believed to control denitrification at the reach scale, such as nitrate concentration, discharge, temperature, and water residence time, and could provide a clearer picture of nitrogen transformations in rivers.     

Nitrogen fixation and denitrification in plankton and periphyton of the Kama River Basin watercourses

The results of studies on molecular nitrogen fixation and denitrification by plankton, epiphytone, and epilithone in a number of natural and anthropogenic waterways of the Kama River Basin are presented for summer and autumn periods of 2005. The nitrogen fixation and denitrification was quantified by acetylene gas chromatography. The phototrophic anoxybiotic purple non-sulfurous bacteria, in particular, of Rhodopseudomonas, Rhodobacter and Rhodocyclus genera, play a significant role in active denitrification in the presence of sulfide-free flow water in the Kama River and its inflows in epilithone, algal-bacterial mats, and biological sewage disposal plants in Perm. On the other hand, the heterocyst cyanobacteria of Anabaena and Aphanizomenon genera had a leading position in active N₂ fixation in the plankton and periphyton of the lower river streams.     

Limitations to measuring riverine denitrification at the whole reach scale: effects of channel geometry,wind velocity,sampling interval,and temperature inputs of N<Subscript>2</Subscript>-enriched groundwater

A model-based approach was recently introduced for measuring riverine denitrification based on measured changes in dissolved N₂ concentration during riverine transport (Laursen & Seitzinger, 2002a). Inputs to the model, including water temperature, channel depth, wind velocity, and time-of-travel between sampling locations, vary greatly among natural systems. Simulations were run by varying the values of these inputs and determining rates of N₂ accumulation in river water and the detection limits for measuring denitrification using this method. Dinitrogen was found to accumulate most rapidly in streams that were shallow, particularly under conditions of low wind velocity. Dissolved N₂ concentrations, modeled in rivers with a diurnal temperature variation of 5 °C and under conditions of no denitrification or 1 mmol N m⁻² h⁻¹, showed that sensitivity of the method can vary as temperatures change. Under low wind conditions and in rivers <1m in depth, this method is capable of detecting denitrification rates as low as 30–100 μmol N m⁻² h⁻¹. This limit of detection should be adequate to measure in situ rates in many North American streams, particularly in agricultural watersheds. In deeper rivers N₂ accumulated more slowly and the method became less sensitive. The results of this study should guide decisions regarding the application of this method based on the specific characteristics of a study reach (channel geometry) and the physical conditions (i.e. wind velocity and water temperature) under which measurements are to be made. The input of N₂-enriched groundwater along a study reach can result in N₂ accumulation that could be misinterpreted as denitrification. Some knowledge of the inputs of groundwater along a reach should also guide decisions regarding the application of this method.     

Mechanism leading to N<Subscript>2</Subscript>O production in wastewater treating biofilm systems

Wastewater treatment plants are known to be important point sources for nitrous oxide (N₂O) in the anthropogenic N cycle. Biofilm based treatment systems have gained increasing popularity in the treatment of wastewater, but the mechanisms and controls of N₂O formation are not fully understood. Here, we review functional groups of microorganism involved in nitrogen (N) transformations during wastewater treatment, with emphasis on potential mechanism of N₂O production in biofilms. Biofilms used in wastewater treatment typically harbour aerobic and anaerobic zones, mediating close interactions between different groups of N transforming organisms. Current models of mass transfer and biomass interactions in biofilms are discussed to illustrate the complex regulation of N₂O production. Ammonia oxidizing bacteria (AOB) are the prime source for N₂O in aerobic zones, while heterotrophic denitrifiers dominate N₂O production in anoxic zones. Nitrosative stress ensuing from accumulation of NO₂ ^? during partial nitrification or denitrification seems to be one of the most critical factors for enhanced N₂O formation. In AOB, N₂O production is coupled to nitrifier denitrification triggered by nitrosative stress, low O₂ tension or low pH. Chemical N₂O production from AOB intermediates (NH₂OH, HNO, NO) released during high NH₃ turnover seems to be limited to surface-near AOB clusters, since diffusive mass transport resistance for O₂ slows down NH₃ oxidation rates in deeper biofilm layers. The proportion of N₂O among gaseous intermediates (NO, N₂O, N₂) in heterotrophic denitrification increases when NO or nitrous acid (HNO₂) accumulates because of increasing NO₂ ^?, or when transient oxygen intrusion impairs complete denitrification. Limited electron donor availability due to mass transport limitation of organic substrates into anoxic biofilm zones is another important factor supporting high N₂O/N₂ ratios in heterotrophic denitrifiers. Biofilms accommodating Anammox bacteria release less N₂O, because Anammox bacteria have no known N₂O producing metabolism and reduce NO₂ ^? to N₂, thereby lowering nitrosative stress to AOB and heterotrophs.     

N<Subscript>2</Subscript>O production by denitrification in an urban river: evidence from isotopes,functional genes,and dissolved organic matter

Rivers are important sources of N₂O emissions into the atmosphere. Nevertheless, N₂O production processes in rivers are not well identified. We measured concentrations and isotopic ratios of N₂O, NH₄ ⁺, NO₂ ^?, and NO₃ ^? in surface water to identify the microbial processes of N₂O production along the Tama River in Japan. We also measured the functional gene abundance of nitrifiers and denitrifiers (amoA-bacteria, nirK, nirS, nosZ clade I, nosZ clade II) together with concentrations of dissolved organic carbon (DOC) and fluorescence intensities of protein and humic components of dissolved organic matter (DOM) to support the elucidation of N₂O production processes. The observed nitrogen (δ¹⁵N) and oxygen (δ¹⁸O) of N₂O were within the expected isotopic range of N₂O produced by nitrate reduction, indicating that N₂O was dominantly produced by denitrification. The positive significant correlation between N₂O_Net concentration and nirK gene abundance implied that nitrifiers and denitrifiers are contributors to N₂O production. Fluorescence intensities of protein and humic components of DOM and concentrations of DOC did not show significant correlations with N₂O concentrations, which suggests that DOC and abundance of DOM components do not control dissolved N₂O. Measurement of isotope ratios of N₂O and its substrates was found to be a useful tool to obtain evidence of denitrification as the main source of N₂O production along the Tama River.     

Nitrate and flooding induce N<Subscript>2</Subscript>O emissions from soybean nodules

Nitrous oxide (N₂O) is one of the three main biogenic greenhouse gases (GHGs) and agriculture represents close to 30 % of the total N₂O net emissions. In agricultural soils, N₂O is emitted by two main microbial processes, nitrification and denitrification, both of which can convert synthetic nitrogen fertilizer into N₂O. Legume-rhizobia symbiosis could be an effective and environmental-friendly alternative to nitrogen fertilization and hence, to mitigate soil N₂O emissions. However, legume crops also contribute to N₂O emissions. A better understanding of the environmental factors involved in the emission of N₂O from nodules would be instrumental for mitigating the release of this GHG gas. In this work, in vivo N₂O emissions from nodulated soybean roots in response to nitrate (0, 1, 2 and 4 mM) and flooding have been measured. To investigate the contribution of rhizobial denitrification in N₂O emission from nodules, plants were inoculated with B. japonicum USDA110 and napA and nosZ denitrification mutants. The results showed that nitrate was essential for N₂O emissions and its concentration enhanced N₂O fluxes showing a statistical linear correlation, being the highest N₂O fluxes obtained with 4 mM nitrate. When inoculated plants grown with 4 mM nitrate were subjected to flooding, a 150- and 830-fold induction of N₂O emission rates from USDA110 and nosZ nodulated roots, respectively, was observed compared to non-flooded plants, especially during long-term flooding. Under these conditions, N₂O emissions from detached nodules produced by the napA mutant were significantly lower (p?<?0.05) than those produced by the wild-type strain (382 versus 1120 nmol N₂O h^?1 g^?1 NFW, respectively). In contrast, nodules from plants inoculated with the nosZ mutant accumulated statistically higher levels of N₂O compared to wild-type nodules (2522 versus nmol 1120 N₂O h^?1 g^?1 NFW, p?<?0.05). These results demonstrate that flooding is an important environmental factor for N₂O emissions from soybean nodules and that B. japonicum denitrification is involved in such emission.     

Whole-system estimation of denitrification in a plains river: a comparison of two methods

Whole-system denitrification in the South Platte River was measured over a 13-month period using an open-channel N₂ method and mass-balance measurements. Concentrations of dissolved N₂ were measured with high precision by membrane-inlet mass spectrometry and estimates of denitrification were based on the mass flux of N₂, after correction for reaeration and groundwater flux. Open-channel estimates of denitrification ranged from 0 to 3.08 g N m^–2 d^–1 and the mean annual rate was 1.62 g N m^–2 d^–1, which corresponds to removal of approximately 34% of the nitrate transported by the river over a distance of 18.5 km. Over the same period of time, estimates of denitrification based on mass-balance measurements ranged from 0.29 to 5.25 g N m^–2 d^–1 and the mean annual rate was 2.11 g N m^–2 d^–1. The two methods revealed similar seasonal patterns of denitrification the highest rates were measured from late April to August and the lowest rates were in winter. Both methods provide whole-system estimates of denitrification in running waters; where reaeration rate coefficients are low and flux of groundwater is well quantified, the open-channel method has fewer sources of uncertainty and is easier to implement.     

Denitrification and N<Subscript>2</Subscript>O emission from forested and cultivated alluvial clay soil

Restored forested wetlands reduce N loads in surface discharge through plant uptake and denitrification. While removal of reactive N reduces impact on receiving waters, it is unclear whether enhanced denitrification also enhances emissions of the greenhouse gas N₂O, thus compromising the water-quality benefits of restoration. This study compares denitrification rates and N₂O:N₂ emission ratios from Sharkey clay soil in a mature bottomland forest to those from an adjacent cultivated site in the Lower Mississippi Alluvial Valley. Potential denitrification of forested soil was 2.4 times of cultivated soil. Using intact soil cores, denitrification rates of forested soil were 5.2, 6.6 and 2.0 times those of cultivated soil at 70, 85 and 100% water-filled pore space (WFPS), respectively. When NO₃ was added, N₂O emissions from forested soil were 2.2 times those of cultivated soil at 70% WFPS. At 85 and 100% WFPS, N₂O emissions were not significantly different despite much greater denitrification rates in the forested soil because N₂O:N₂ emission ratios declined more rapidly in forested soil as WFPS increased. These findings suggest that restoration of forested wetlands to reduce NO₃ in surface discharge will not contribute significantly to the atmospheric burden of N₂O.     

DOC and N<Subscript>2</Subscript>O dynamics in upland and peatland forest soils after clear-cutting and soil preparation

Forest clear-cutting followed by soil preparation means disturbance for soil microorganisms and disruption of N and C cycles. We measured fluxes of N₂O and dissolved organic carbon (DOC) in upland soil (podzol) and adjacent peat within a clear-cut forest catchment. Both soil types behaved in a similar way, showing net uptake of N₂O in the first year after the clear-cutting, and turning to net release in the second. The N₂O flux dynamics were similar to those of N content in logging residues, as reported from a nearby site. As organic matter is used in the food web of the decomposers, we attempted to explain the dynamics of N₂O uptake and release by measuring the concurrent dynamics of the low molecular weight (LMW) fraction and the aromaticity of DOC in a soil solution. The labile and most readily available LMW fractions of DOC were nearly absent in the year following the clear-cutting, but rose after two years. The more refractory high molecular weight (HMW) fraction of DOC decreased two years after the clear-cutting. The first year’s net uptake of N₂O could be accounted for by the growth of decomposer biomass in the logging residues and detritus from the degenerating ground vegetation, resulting in immobilization of nitrogen. Simultaneously, the labile, LMW fraction of DOC became almost completely exhausted. The low availability of the LMW fraction could retard the growth and cause the accumulated decomposer biomass to collapse. During the following winter and summer the fraction of LMW clearly increased, followed by increased N₂O emissions. The presence of LMW DOC fractions, not the concentration of DOC, seems to be an important controller for N₂O liberation after a major disturbance such as clear-cutting and site preparation. The complex connection between DOC characteristics, nitrification or denitrification merits further studies.     

Co-occurrence of in-stream nitrogen fixation and denitrification across a nitrogen gradient in a western U.S. watershed

It is frequently assumed that nitrogen (N₂) fixation and denitrification do not co-occur in streams because each process should be favored under different concentrations of dissolved inorganic nitrogen (DIN), and therefore these processes are rarely quantified together. We asked if these processes could co-exist by conducting a spatial survey of N₂ fixation using acetylene reduction and denitrification using acetylene block [with and without amendments of carbon (C) as glucose and nitrogen (N) as nitrate]. Rates were measured on rocks and sediment in 8 southeastern Idaho streams encompassing a DIN gradient of 26–615 µg L^?1. Sampling at each site was repeated in summer 2015 and 2016. We found that both denitrification and N₂ fixation occurred across the gradient of DIN concentrations, with N₂ fixation occurring primarily on rocks and denitrification occurring in sediment. N₂ fixation rates on rocks significantly decreased 100× across the DIN gradient in 1 year of the study, and amended (with N and C) denitrification rates increased 10× across the DIN gradient in both years. Multiple linear regression and partial least squares models with environmental characteristics measured at the scale of entire stream reaches showed that C and phosphorus were positive predictors of amended and unamended denitrification rates, but no significant model could explain N₂ fixation rates across all streams and years. This, coupled with the observation that detectable rates of N₂ fixation occurred primarily on rocks and denitrification occurred primarily on sediment, suggests that microhabitat scale factors may better predict the co-occurrence of these processes within stream reaches. Overlooking the potential co-occurrence of N₂ fixation and denitrification in stream ecosystems will impede understanding by oversimplifying the contribution of each process to the N cycle.     

The role of N<Subscript>2</Subscript> fixation in alleviating N limitation in wetland metaphyton: enzymatic,isotopic, and elemental evidence

The role of nitrogen (N₂) fixation in balancing N supply to wetland metaphyton was assessed by comparing primary production with enzymatic, isotopic, and elemental correlates. Primary production, N₂ fixation (acetylene reduction, AR), phosphatase activity, C:N:P ratio, and N isotopic composition of metaphyton were measured along a nutrient gradient in a freshwater marsh during May through September 2004. N₂ fixation and phosphatase activity in metaphyton were negatively correlated with inorganic N and P concentrations, respectively. Although metaphyton N₂ fixation demonstrated a clear spatial pattern along the nutrient gradient, N₂ fixation rates varied monthly and decreased sharply in September. However, the percent contribution of N₂ fixation to N uptake by metaphyton consistently decreased throughout the summer. Furthermore, the decreased contribution of N₂ fixation to N uptake corresponded with an increase in metaphyton N content during the growing season. Nitrogen isotopic data suggested the sustained importance of an atmospheric N₂ source through September at the most downstream (nutrient poor) site even though the percent contribution of N₂ fixition to N uptake was lowest in that month. This suggests that metaphyton were efficiently accumulating and recycling fixed N₂ in support of primary production. Over the course of the summer, metaphyton primary production showed a weak inverse correlation with metaphyton phosphatase activity (r ² = 0.58). The largest residuals in this regression corresponded to the largest vartiation in metaphyton N content. When metaphyton primary production was normalized to metaphyton N content, production rates for the entire growing season were more strongly inversely correlated with metaphyton phosphatase activity (r ² = 0.78). Results of the study suggest that N₂ fixation in N poor areas may adequately supplement community N requirements in metaphyton, thereby causing limitation by other elemental resources such as P.     

Seasonal variation in soil CO<Subscript>2</Subscript> efflux in evergreen coniferous and broad-leaved deciduous forests in a cool-temperate forest,central Korea

We measured the soil surface CO₂ efflux (R _S) from January 2005 to December 2006 in two neighboring stands in Gwangneung Forest, central Korea: evergreen coniferous forest (Abies holophylla, stand A) and broad-leaved deciduous forest (Quercus-dominated, stand Q). Regarding seasonal variation, R _S rate was low during the winter and early spring months in each stand and peaked in late July [1170 (stand A) and 1130 (stand Q) in 2005, and 1000 (stand A) and 740 (stand Q) mg CO₂ m⁻² h⁻¹ in 2006]. R _S rate was higher in stand A than in stand Q during most of the growing season. The pattern of summer rainfall differed between 2005 and 2006. R _S rate for both stands was suppressed significantly by the droughts in June 2005 and September 2006. After the heavy rainfall of July 2006, R _S rate was lower than in July 2005 in both stands, but this decrement was much greater in stand Q than in stand A. In midsummer (August) 2006, under higher soil temperature (ST) and lower soil water content (SWC) conditions than in August 2005, R _S rate of stand A was lower than that in August 2005, whereas stand Q showed no marked change. The exponential relationship between ST and R _S accounted for approximately 91–97% of the R _S variability in each stand and in each year. In stand A, the application of a second-order polynomial function indicated a significant correlation between SWC and R _S when the soil was warm (ST > 15°C). Our results suggest that the seasonality of R _S is strongly affected by the pattern of summer rainfall even in an Asia monsoon climate regime. In addition, the vegetation type (i.e., evergreen coniferous forest vs. broad-leaved deciduous forest) plays a significant role in response of R _S to various environmental fluctuations such as drought, heavy rainfall, and hot-dry condition.     

Nitrification and denitrification in a midwestern stream containing high nitrate: in situ assessment using tracers in dome-shaped incubation chambers

The extent to which in-stream processes alter or remove nutrient loads in agriculturally impacted streams is critically important to watershed function and the delivery of those loads to coastal waters. In this study, patch-scale rates of in-stream benthic processes were determined using large volume, open-bottom benthic incubation chambers in a nitrate-rich, first to third order stream draining an area dominated by tile-drained row-crop fields. The chambers were fitted with sampling/mixing ports, a volume compensation bladder, and porewater samplers. Incubations were conducted with added tracers (NaBr and either ¹⁵N[NO₃ ^?], ¹⁵N[NO₂ ^?], or ¹⁵N[NH₄ ⁺]) for 24–44 h intervals and reaction rates were determined from changes in concentrations and isotopic compositions of nitrate, nitrite, ammonium and nitrogen gas. Overall, nitrate loss rates (220–3,560 μmol N m^?2 h^?1) greatly exceeded corresponding denitrification rates (34–212 μmol N m^?2 h^?1) and both of these rates were correlated with nitrate concentrations (90–1,330 μM), which could be readily manipulated with addition experiments. Chamber estimates closely matched whole-stream rates of denitrification and nitrate loss using ¹⁵N. Chamber incubations with acetylene indicated that coupled nitrification/denitrification was not a major source of N₂ production at ambient nitrate concentrations (175 μM), but acetylene was not effective for assessing denitrification at higher nitrate concentrations (1,330 μM). Ammonium uptake rates greatly exceeded nitrification rates, which were relatively low even with added ammonium (3.5 μmol N m^?2 h^?1), though incubations with nitrite demonstrated that oxidation to nitrate exceeded reduction to nitrogen gas in the surface sediments by fivefold to tenfold. The chamber results confirmed earlier studies that denitrification was a substantial nitrate sink in this stream, but they also indicated that dissolved inorganic nitrogen (DIN) turnover rates greatly exceeded the rates of permanent nitrogen removal via denitrification.     

Direct flux and 15N tracer methods for measuring denitrification in forest soils

Estimates of denitrification are one of the key uncertainties in the terrestrial nitrogen (N) cycle, primarily because reliable measurements of this highly variable process—especially the production of its terminal product (N₂)—are difficult to obtain. We evaluated the ability of gas-flow soil core and ¹⁵N tracer methods to provide reliable estimates of denitrification in forest soils. Our objectives were to: (1) describe and present typical results from new gas-flow soil core and in situ ¹⁵N tracer methods for measuring denitrification, (2) discuss factors that affect the relevance of these methods to actual in situ denitrification, and (3) compare denitrification estimates produced by the two methods for a series of sites in a northern hardwood forest ecosystem. Both methods were able to measure accumulations of N₂ over relatively short (2–5 h) incubations of either unamended or tracer-amended intact soils. Denitrification rates measured by the direct flux soil core method were very sensitive to incubation oxygen (O₂) concentration and decreased with increased O₂ levels. Denitrification rates measured by the in situ ¹⁵N tracer method were very sensitive to the ¹⁵N content of the nitrate (NO₃ ^?) pool undergoing denitrification, which limits the applicability of this method for quantifying denitrification in N-poor ecosystems. While its ability to provide accurate estimates of denitrification was limited, the ¹⁵N tracer method provided estimates of the short-term abiotic and biotic transformations of atmospheric N deposition to gas. Furthermore, results suggest that denitrification is higher and that N₂O:N₂ ratios are lower (<0.02) than previously thought in the northern hardwood forest and that short-term abiotic and biotic transformations of atmospheric N deposition to gas are significant in this ecosystem.     

Enhanced biological nitrogen removal and N<Subscript>2</Subscript>O emission characteristics of the intermittent aeration activated sludge process

Enhanced biological nitrogen removal processes are necessarily required to cope with more stringent wastewater discharging regulations, especially for wastewater with low level of organic carbon to nitrogen ratios. The intermittent aeration activated sludge process has been received comprehensive attention over the past decades, due to its excellent performance in nitrogen removal and remarkable reduction of energy consumption. Recent advances for this technology was reviewed from aspects of characteristics of system, factors affecting nitrogen removal, nitrous oxide (N₂O) emission and its control, and application of the technology and its operation control. Finally, future development was proposed. In the intermittent aeration activated sludge process, aeration duration should be controlled for adequate nitrification and non-aeration duration should be adequate for complete denitrification, and these would benefit both nitrogen removal and N₂O mitigation. The step feed strategy could be applied to enhance the better utilization of influent organic carbon for nitrogen removal. Dissolved oxygen (DO) and aerobic duration both affected nitrogen removal in particular that via nitrite in the intermittent aeration process. Nitrite should be removed efficiently to avoid a high N₂O emission under both anoxic and aerobic conditions. Intermittent aeration activated sludge process has been applied in the treatment of various wastewaters, such as municipal wastewater, swine wastewater, anaerobic effluents and landfill leachate. For practical application, DO, pH and oxidation–reduction potential could be used as indices for controlling nitrogen removal and N₂O mitigation. Microbial ecology in the intermittent aeration activated sludge process should be specifically focused in future studies.     

Total denitrification and the ratio between N2O and N2 during the growth of spring barley

Summary Total denitrification (N₂O+N₂) and nitrous oxide emission were measured on intact soil cores using the acetylene inhibition technique.Total denitrification from the depth 0–8 cm during the growth period from April to August was 7 kg N/ha from plots supplied with 30 kg N/ha and 19 kg N/ha from plots supplied with 120 kg N/ha. The amounts of precipitation, plant growth, and N application were found to affect the denitrification rate. These factors also affected the ratio (N₂O+N₂)/N₂O, which varied from 1.0 to 7.2. Plant growth and precipitation increased the proportion of N₂ produced, whereas a high nitrate content increased the proportion of N₂O.     

Influence of hydrological connectivity of riverine wetlands on nitrogen removal via denitrification

Wetland ecosystems in agricultural areas often become progressively more isolated from main water bodies. Stagnation favors the accumulation of organic matter as the supply of electron acceptors with water renewal is limited. In this context it is expected that nitrogen recycling prevails over nitrogen dissipation. To test this hypothesis, denitrification rates, fluxes of dissolved oxygen (SOD), inorganic carbon (DIC) and nitrogen and sediment features were measured in winter and summer 2007 on 22 shallow riverine wetlands in the Po River Plain (Northern Italy). Fluxes were determined from incubations of intact cores by measurement of concentration changes or isotope pairing in the case of denitrification. Sampled sites were eutrophic to hypertrophic; 10 were connected and 12 were isolated from the adjacent rivers, resulting in large differences in nitrate concentrations in the water column (from <5 to 1,133 μM). Benthic metabolism and denitrification rates were investigated by two overarching factors: season and hydrological connectivity. SOD and DIC fluxes resulted in respiratory quotients greater than one at most sampling sites. Sediment respiration was coupled to both ammonium efflux, which increased from winter to summer, and nitrate consumption, with higher rates in river-connected wetlands. Denitrification rates measured in river-connected wetlands (35–1,888 μmol N m^?2 h^?1) were up to two orders of magnitude higher than rates measured in isolated wetlands (2–231 μmol N m^?2 h^?1), suggesting a strong regulation of the process by nitrate availability. These rates were also significantly higher in summer (9–1,888 μmol N m^?2 h^?1) than in winter (2–365 μmol N m^?2 h^?1). Denitrification supported by water column nitrate (D_W) accounted for 60–100% of total denitrification (Dtot); denitrification coupled to nitrification (D_N) was probably controlled by limited oxygen availability within sediments. Denitrification efficiency, calculated as the ratio between N removal via denitrification and N regeneration, and the relative role of denitrification for organic matter oxidation, were high in connected wetlands but not in isolated sites. This study confirms the importance of restoring hydraulic connectivity of riverine wetlands for the maintenance of important biogeochemical functions such as nitrogen removal via denitrification.     

Nitrogen removal in a wastewater treatment plant through biofilters: nitrous oxide emissions during nitrification and denitrification

In order to estimate N₂O emissions from immersed biofilters during nitrogen removal in tertiary treatments at urban wastewater treatment plants (WWTPs), a fixed culture from the WWTP of “Seine Centre” (Paris conurbation) was subjected to lab-scale batch experiments under various conditions of oxygenation and a gradient of methanol addition. The results show that during nitrification, N₂O emissions are positively related to oxygenation (R ² = 0.99). However, compared to the rates of ammonium oxidation, the percentage of emitted N₂O is greater when oxygenation is low (0.5–1 mgO₂ L⁻¹), representing up to 1% of the oxidized ammonium (0.4% on average). During denitrification, the N₂O emission reaches a significant peak when the quantity of methanol allows denitrification of between 66% and 88%. When methanol concentrations lead to a denitrification of close to 100%, the flows of N₂O are much lower and represent on average 0.2% of the reduced nitrate. By considering these results, we can estimate, the emissions of N₂O during nitrogen removal, at the “Seine Centre” WWTP, to approximately 38 kgN-N₂O day⁻¹.