Impact of carbon source on nitrous oxide emission from anoxic/oxic biological nitrogen removal process and identification of its emission sources

Wastewater treatment is an important source of nitrous oxide (N₂O), which is a strong greenhouse gas and dominate ozone-depleting substance. The purpose of this study was to evaluate the effect of carbon source on N₂O emission from anoxic/oxic biological nitrogen removal process. The mechanisms of N₂O emission were also studied. Long-term experiments were operated to evaluate the effect of three different carbon sources (i.e., glucose, sodium acetate, and soluble starch) on N₂O emission characteristics. And batch experiments, in the presence or absence of specific inhibitors, were carried out to identify the sources of N₂O emission. The ammonia-oxidizing bacteria (AOB) and denitrifiers community compositions under different circumstances were also analyzed based on which the underlying mechanisms of N₂O emission were elucidated. The conversion ratios of N₂O in reactors with glucose, sodium acetate, and soluble starch were 5.3 %, 8.8 %, and 2.8 %, respectively. The primary process responsible for N₂O emission was nitrifier denitrification by Nitrosomonas-like AOB, while denitrification by heterotrophic denitrifiers acted as the sink. Reactor with sodium acetate showed the highest N₂O emission, together with the highest nitrogen and phosphate removal ratios. Carbon source has a significant impact on N₂O emission quantity and relatively minor effect on its production mechanism.     

Calculation of σz and H for an Observed Vertical Profile of Concentration

ABSTRACT

In the present work, nitrous oxide emissions were estimated [mg/L] by the use of lysimeters under the closed chamber technique for a six month period. The lysimeters were classified by the type of irrigation used: one for drinking water, and the other for treated wastewater. Each lysimeter had two different types of soil (sand and clay), based on the types of soil in Chihuahua City, Mexico. An additional classification based on the depth was done (reticular and vadose zone). Each zone collected gas by the use of a closed chamber technique, allowing the samples to be taken for subsequent quantification and analysis by gas chromatography. A statistical analysis of variance (ANOVA) and principal components analysis (PCA) were conducted to identify the most influential variables or parameters in the formation of nitrous oxide. The variables that were considered for analysis were total Kjeldahl nitrogen (TKN), ammoniacal nitrogen (NH3-N), nitrate nitrogen (NO3-N), and nitrite nitrogen (NO2-N), along with meteorological parameters. In total, 58944 mg/L of N2O were emitted during the measurement period. The results showed that concentration emissions of N2O where the type of soil is sandy were smaller than those of clay soil, while the mean concentration in the vadose zone was higher than those in the reticular zone, regardless the type of soil. The parameters that showed greater influence in the N2O emissions were NO2-N and NO3-N concentrations. Temperature also played an important role in the emissions (the highest emissions were emitted during the cold months). Furthermore, denitrification appeared to be the dominant process in the production of nitrous oxide in soils.

Implications: Nitrous oxide (N₂O) emissions produced in lysimeters with two types of soil (sand and clay) at two different depths (vadose and reticular zones) using treated waste water showed that the higher emissions of N₂O are derived from clay soils in vadose zone; it could be due to the formation of clogging that favors the formation of anoxic conditions for the denitrification process. The parameters that showed more influence in the N₂O emissions were nitrite (NO₂-N) and nitrate (NO₃-N) concentrations along with the temperature.     

Field study of nitrous oxide production with in situ aeration in a closed landfill site

Nitrous oxide (N₂O) has gained considerable attention as a contributor to global warming and depilation of stratospheric ozone layer. Landfill is one of the high emitters of greenhouse gas such as methane and N₂O during the biodegradation of solid waste. Landfill aeration has been attracted increasing attention worldwide for fast, controlled and sustainable conversion of landfills into a biological stabilized condition, however landfill aeration impel N₂O emission with ammonia removal. N₂O originates from the biodegradation, or the combustion of nitrogen-containing solid waste during the microbial process of nitrification and denitrification. During these two processes, formation of N₂O as a by-product from nitrification, or as an intermediate product of denitrification. In this study, air was injected into a closed landfill site and investigated the major N₂O production factors and correlations established between them. The in-situ aeration experiment was carried out by three sets of gas collection pipes along with temperature probes were installed at three different distances of one, two and three meter away from the aeration point; named points A-C, respectively. Each set of pipes consisted of three different pipes at three different depths of 0.0, 0.75 and 1.5 m from the bottom of the cover soil. Landfill gases composition was monitored weekly and gas samples were collected for analysis of nitrous oxide concentrations. It was evaluated that temperatures within the range of 30–40°C with high oxygen content led to higher generation of nitrous oxide with high aeration rate. Lower O₂ content can infuse N₂O production during nitrification and high O₂ inhibit denitrification which would affect N₂O production. The findings provide insights concerning the production potentials of N₂O in an aerated landfill that may help to minimize with appropriate control of the operational parameters and biological reactions of N turnover.

Implications: Investigation of nitrous oxide production potential during in situ aeration in an old landfill site revealed that increased temperatures and oxygen content inside the landfill site are potential factors for nitrous oxide production. Temperatures within the range of optimum nitrification process (30–40°C) induce nitrous oxide formation with high oxygen concentration as a by-product of nitrogen turnover. Decrease of oxygen content during nitrification leads increase of nitrous oxide production, while temperatures above 40°C with moderate and/or low oxygen content inhibit nitrous oxide generation.     

Indirect nitrous oxide emission from a nitrogen saturated spruce forest and general accuracy of the IPCC methodology

The relevance of indirect N₂O emission is a controversial topic which is subject to much uncertainty. Only a small number of studies measure the indirect N₂O emission at the interface from soil to stream. In addition, the majority of studies undertaken only cover a short-term period (<1 year). Therefore, limited information is available regarding the influence of seasonal or event effects, nor is there much information as to whether indirect N₂O emissions are reflected by N₂O in soil solutions. The present study aimed at clarifying these two questions along with the general relevance of dissolved nitrous oxide. A wetness gradient involving soil solutions of different soil types and surface waters within an N-saturated forest catchment (3.2 ha) was monitored over a period of 1 year. N₂O concentrations in soil solutions (0.09–16.6 μg N l⁻¹) were affected by events such as dry–wet cycles but did not reflect to the actual, indirect N₂O emission at the soil-stream interface. It was assumed that N₂O emission was due to N transformation processes. The N₂O concentration at the spring was three times higher than the N₂O concentrations in the soil solutions. Nevertheless, indirect N₂O emission was still subordinate (<1%) to the direct emission of N₂O. The weekly amount of indirect N₂O emissions depended only on the stream flow rate (62% of the total annual amount). For this reason it was necessary to measure indirect N₂O emission at short intervals and at the interface between soil and stream over a longer time period. Our results and the results of the reviewed studies show that the default IPCC emission factor (EF5-g=1.5%) overestimates the indirect N₂O emission from ecosystems. The emission factor should therefore be lowered to about 0.1–0.3%. In addition, the results indicate that indirect N₂O emission is an insignificant pathway in the N cycle of most ecosystems. However, final judgement will depend on long-term studies.     

Mitigating Global Warming Potentials of Methane and Nitrous Oxide Gases from Rice Paddies under different irrigation regimes

A field experiment was conducted in Bangladesh Agricultural University Farm to investigate the mitigating effects of soil amendments such as calcium carbide, calcium silicate, phosphogypsum, and biochar with urea fertilizer on global warming potentials (GWPs) of methane (CH₄) and nitrous oxide (N₂O) gases during rice cultivation under continuous and intermittent irrigations. Among the amendments phosphogypsum and silicate fertilizer, being potential source of electron acceptors, decreased maximum level of seasonal CH₄ flux by 25–27 % and 32–38 % in continuous and intermittent irrigations, respectively. Biochar and calcium carbide amendments, acting as nitrification inhibitors, decreased N₂O emissions by 36–40 % and 26–30 % under continuous and intermittent irrigations, respectively. The total GWP of CH₄ and N₂O gases were decreased by 7–27 % and 6–34 % with calcium carbide, phosphogypsum, and silicate fertilizer amendments under continuous and intermittent irrigations, respectively. However, biochar amendments increased overall GWP of CH₄ and N₂O gases.     

Seasonal variations of CH(4) and N(2)O emissions in response to water management of paddy fields located in Southeast China

Water management is one of the most important practices that affect methane (CH₄) and nitrous oxide (N₂O) emissions from paddy fields. A field experiment was designed to study the effects of controlled irrigation (CI) on CH₄ and N₂O emissions from paddy fields, with traditional irrigation (TI) as the control. The effects of CI on CH₄ and N₂O emissions from paddy fields were very clear. The peaks of CH₄ emissions from the CI paddies were observed 1-2 d after the water layer disappeared. Afterward, the emissions reduced rapidly and remained low until the soil was re-flooded. A slight increase of CH₄ emission was observed in a short period after re-flooding. N₂O emissions peaks from CI paddies were all observed 8-10 d after the fertilization at the WFPS ranging from 78.1% to 85.3%. Soil drying caused substantial N₂O emissions, whereas no substantial N₂O emissions were observed when the soil was re-wetted after the dry phase. Compared with TI, the cumulative CH₄ emissions from the CI fields were reduced by 81.8% on the average, whereas the cumulative N₂O emissions were increased by 135.4% on the average. The integrative global warming potential of CH₄ and N₂O on a 100-year horizon decreased by 27.3% in the CI paddy fields, whereas no significant difference in the rice yield was observed between the CI and TI fields. These results suggest that CI can effectively mitigate the integrative greenhouse effect caused by CH₄ and N₂O emissions from paddy fields while ensuring the rice yield.     

Impacts of feedlot floor condition,deposition frequency,and inhibitors on N2O and CH4 emissions from feedlot dung and urine patches

Patches of dung and urine are major contributors to the feedlot gas emissions. This study investigated the impacts of dung deposition frequency (partly reflecting animal stocking density of a feedlot), dairy feedlot floor conditions (old floor indicated with the presence of consolidated manure pad [CMP] vs. new floor with the absence of consolidated manure pad [CMPn]), and application of dicyandiamide (DCD) and hydroquinone (HQ) on nitrous oxide (N₂O) and methane (CH₄) emissions from patches in the laboratory, and the integrative impacts were expressed in terms of global warming potential (CO₂-equivalent). Dung deposition frequency, feedlot floor condition, and application of inhibitors showed inverse impacts on N₂O and CH₄ emissions from patches. Greenhouse gas (GHG) emissions from the dung, urine, and dung+urine patches on the CMP feedlot surface were approximately 7.48, 87.35, and 7.10 times those on the CMPn feedlot surface (P < 0.05). Meanwhile, GHG emissions from CMP and CMPn feedlot surfaces under high deposition frequency condition were approximately 10 and 1.7 times those under low-frequency condition. Moreover, application of HQ slightly reduced the GHG emission from urine patches, by 14.9% (P > 0.05), while applying DCD or DCD+HQ significantly reduced the GHG, by 60.3% and 65.0%, respectively (P < 0.05). Overall, it is necessary to include feedlot management such as animal stocking density and feedlot floor condition to the process of determining emission factors for feedlots. In the future, field measurements to quantitatively evaluate the relative contribution of nitrification and denitrification to the N₂O emissions of feedlot surfaces are highly required for effective N₂O control.

Implications: This study shows that feedlot CH₄ and N₂O emissions inversely respond to the dicyandiamide (DCD) application. Applying DCD significantly reduces GHG emissions of feedlot urine patches. Feedlot floor condition and stocking density strongly impact feedlot GHG emissions. Including feedlot floor condition and stocking density in the feedlot EF determining process is necessary.     

Nitric oxide and nitrous oxide emission from Hungarian forest soils; linked with atmospheric N-deposition

Studies of forest nitrogen (N) budgets generally measure inputs from the atmosphere in wet and dry deposition and outputs via hydrologic export. Although denitrification has been shown to be important in many wetland ecosystems, emission of N oxides from forest soils is an important, and often overlooked, component of an ecosystem N budget. During 1 year (2002–03), emissions of nitric oxide (NO) and nitrous oxide (N₂O) were measured from Sessile oak and Norway spruce forest soils in northeast Hungary. Accumulation in small static chambers followed by gas chromatography-mass spectrometry detection was used for the estimation of N₂O emission flux. Because there are rapid chemical reactions of NO and ozone, small dynamic chambers were used for in situ NO flux measurements. Average soil emissions of NO were 1.2 and 2.1 μg N m⁻² h⁻¹, and for N₂O were 15 and 20 μg N m⁻² h⁻¹, for spruce and oak soils, respectively. Due to the relatively high soil water content, and low C/N ratio in soil, denitrification processes dominate, resulting in an order of magnitude greater N₂O emission rate compared to NO. The previously determined N balance between the atmosphere and the forest ecosystem was re-calculated using these soil emission figures. The total (dry+wet) atmospheric N-deposition to the soil was 1.42 and 1.59 g N m⁻² yr⁻¹ for spruce and oak, respectively, while the soil emissions are 0.14 and 0.20 g N m⁻² yr⁻¹. Thus, about 10–13% of N compounds deposited to the soil, mostly as and , were transformed in the soil and emitted back to the atmosphere, mostly as greenhouse gas (N₂O).     

The effect of diet manipulation on nitrous oxide and methane emissions from manure application to incubated grassland soils

Changes to agricultural management, particularly of the nitrogen (N) input to farms, have great potential for mitigating emissions of N containing gases, especially the greenhouse gas nitrous oxide (N₂O). Manipulating diets fed to livestock is a potential method for controlling N excretion and emissions of greenhouse gases (GHG's) to the atmosphere. We selected three slurries derived from sheep that had been fed, either ensiled ryegrass (Lolium hybridicum), lucerne (Medicago sativa) or kale (Brassica oleracea) and applied them to a grassland soil from the UK in a laboratory experiment using a special He/O₂ atmosphere incubation facility. The resulting fluxes of N₂O, CH₄ and N₂ were measured, with the largest total N fluxes generated by the ryegrass slurry treatment (14.23 ryegrass, 10.84 lucerne, 13.88 kale and 4.40 kg N ha⁻¹ from the control). Methane was emitted only from the ryegrass slurry treatment. The isotopomer signatures for N₂O in the control and lucerne slurry treatments indicated that denitrification was the main process responsible for N₂O emissions.     

Effect of topography on nitrous oxide emissions from winter wheat fields in Central France

We assessed nitrous oxide (N₂O) emissions at shoulder and foot-slope positions along three sloping sites (1.6–2.1%) to identify the factors controlling the spatial variations in emissions. The three sites received same amounts of total nitrogen (N) input at 170 kg N ha⁻¹. Results showed that landscape positions had a significant, but not consistent effect on N₂O fluxes with larger emission in the foot-slope at only one of the three sites. The effect of soil inorganic N (NH₄⁺ + NO₃⁻) contents on N₂O fluxes (r² = 0.55, p < 0.001) was influenced by water-filled pore space (WFPS). Soil N₂O fluxes were related to inorganic N at WFPS > 60% (r² = 0.81, p < 0.001), and NH₄⁺ contents at WFPS < 60% (r² = 0.40, p < 0.01), respectively. Differences in WFPS between shoulder and foot-slope correlated linearly with differences in N₂O fluxes (r² = 0.45, p < 0.001). We conclude that spatial variations in N₂O emission were regulated by the influence of hydrological processes on soil aeration intensity.     

Impact of biochar application to a Mediterranean wheat crop on soil microbial activity and greenhouse gas fluxes

Biochar has been recently proposed as a management strategy to improve crop productivity and global warming mitigation. However, the effect of such approach on soil greenhouse gas fluxes is highly uncertain and few data from field experiments are available. In a field trial, cultivated with wheat, biochar was added to the soil (3 or 6 kg m⁻²) in two growing seasons (2008/2009 and 2009/2010) so to monitor the effect of treatments on microbial parameters 3 months and 14 months after char addition. N₂O, CH₄ and CO₂ fluxes were measured in the field during the first year after char addition. Biochar incorporation into the soil increased soil pH (from 5.2 to 6.7) and the rates of net N mineralization, soil microbial respiration and denitrification activity in the first 3 months, but after 14 months treated and control plots did not differ significantly. No changes in total microbial biomass and net nitrification rate were observed. In char treated plots, soil N₂O fluxes were from 26% to 79% lower than N₂O fluxes in control plots, excluding four sampling dates after the last fertilization with urea, when N₂O emissions were higher in char treated plots. However, due to the high spatial variability, the observed differences were rarely significant. No significant differences of CH₄ fluxes and field soil respiration were observed among different treatments, with just few exceptions. Overall the char treatments showed a minimal impact on microbial parameters and GHG fluxes over the first 14 months after biochar incorporation.     

Effects of land use conversion and fertilization on CH<Subscript>4</Subscript> and N<Subscript>2</Subscript>O fluxes from typical hilly red soil

Land use conversion and fertilization have been widely reported to be important managements affecting the exchanges of greenhouse gases between soil and atmosphere. For comprehensive assessment of methane (CH₄) and nitrous oxide (N₂O) fluxes from hilly red soil induced by land use conversion and fertilization, a 14-month continuous field measurement was conducted on the newly converted citrus orchard plots with fertilization (OF) and without fertilization (ONF) and the conventional paddy plots with fertilization (PF) and without fertilization (PNF). Our results showed that land use conversion from paddy to orchard reduced the CH₄ fluxes at the expense of increasing the N₂O fluxes. Furthermore, fertilization significantly decreased the CH₄ fluxes from paddy soils in the second stage after conversion, but it failed to affect the CH₄ fluxes from orchard soils, whereas fertilizer applied to orchard and paddy increased soil N₂O emissions by 68 and 113.9 %, respectively. Thus, cumulative CH₄ emissions from the OF were 100 % lower, and N₂O emissions were 421 % higher than those from the PF. Although cumulative N₂O emissions were stimulated in the newly converted orchard, the strong reduction of CH₄ led to lower global warming potentials (GWPs) as compared to the paddy. Besides, fertilization in orchard increased GWPs but decreased GWPs of paddy soils. In addition, measurement of soil moisture, temperature, dissolved carbon contents (DOCs), and ammonia (NH₄ ⁺-N) and nitrate (NO₃ ^?-N) contents indicated a significant variation in soil properties and contributed to variations in soil CH₄ and N₂O fluxes. Results of this study suggest that land use conversion from paddy to orchard would benefit for reconciling greenhouse gas mitigation and citrus orchard cultivation would be a better agricultural system in the hilly red soils in terms of greenhouse gas emission. Moreover, selected fertilizer rate applied to paddy would lead to lower GWPs of CH₄ and N₂O. Nevertheless, more field measurements from newly converted orchard are highly needed to gain an insight into national and global accounting of CH₄ and N₂O emissions.     

A study on the evaluations of emission factors and uncertainty ranges for methane and nitrous oxide from combined-cycle power plant in Korea

In this research, in order to develop technology/country-specific emission factors of methane (CH₄) and nitrous oxide (N₂O), a total of 585 samples from eight gas-fired turbine combined cycle (GTCC) power plants were measured and analyzed. The research found that the emission factor for CH₄ stood at “0.82 kg/TJ”, which was an 18 % lower than the emission factor for liquefied natural gas (LNG) GTCC “1 kg/TJ” presented by Intergovernmental Panel on Climate Change (IPCC). The result was 8 % up when compared with the emission factor of Japan which stands at “0.75 kg/TJ”. The emission factor for N₂O was “0.65 kg/TJ”, which is significantly lower than “3 kg/TJ” of the emission factor for LNG GTCC presented by IPCC, but over six times higher than the default N₂O emission factor of LNG. The evaluation of uncertainty was conducted based on the estimated non-CO₂ emission factors, and the ranges of uncertainty for CH₄ and N₂O were between ?12.96 and +13.89 %, and ?11.43 and +12.86 %, respectively, which is significantly lower than uncertainties presented by IPCC. These differences proved that non-CO₂ emissions can change depending on combustion technologies; therefore, it is vital to establish country/technology-specific emission factors.     

Processes and factors controlling N₂O production in an intensively managed low carbon calcareous soil under sub-humid monsoon conditions

An automated system for continuous measurement of N₂O fluxes on an hourly basis was employed to study N₂O emissions in an intensively managed low carbon calcareous soil under sub-humid temperate monsoon conditions. N₂O emissions occurred mainly within two weeks of application of NH₄⁺-based fertilizer and total N₂O emissions in wheat (average 0.35 or 0.21 kg N ha⁻¹ season⁻¹) and maize (average 1.47 or 0.49 kg N ha⁻¹ season⁻¹) under conventional and optimum N fertilization (300 and 50-122 kg N ha⁻¹, respectively) were lower than previously reported from low frequency measurements. Results from closed static chamber showed that N₂O was produced mainly from nitrification of NH₄⁺-based fertilizer, with little denitrification occurring due to limited readily oxidizable carbon and low soil moisture despite consistently high soil nitrate-N concentrations. Significant reductions in N₂O emissions can be achieved by optimizing fertilizer N rates, using nitrification inhibitors, or changing from NH₄⁺- to NO₃^ˉ-based fertilizers.     

Greenhouse gas emissions from penguin guanos and ornithogenic soils in coastal Antarctica: Effects of freezing–thawing cycles

In coastal Antarctica, freezing and thawing influence many physical, chemical and biological processes for ice-free tundra ecosystems, including the production of greenhouse gases (GHGs). In this study, penguin guanos and ornithogenic soil cores were collected from four penguin colonies and one seal colony in coastal Antarctica, and experimentally subjected to three freezing–thawing cycles (FTCs) under ambient air and under N₂. We investigated the effects of FTCs on the emissions of three GHGs including nitrous oxide (N₂O), carbon dioxide (CO₂) and methane (CH₄). The GHG emission rates were extremely low in frozen penguin guanos or ornithogenic soils. However, there was a fast increase in the emission rates of three GHGs following thawing. During FTCs, cumulative N₂O emissions from ornithogenic soils were greatly higher than those from penguin guanos under ambient air or under N₂. The highest N₂O cumulative emission of 138.24 μg N₂O–N kg^?1 was observed from seal colony soils. Cumulative CO₂ and CH₄ emissions from penguin guanos were one to three orders of magnitude higher than those from ornithogenic soils. The highest cumulative CO₂ (433.0 mgCO₂–C kg^?1) and CH₄ (2.9 mgCH₄–C kg^?1) emissions occurred in emperor penguin guanos. Penguin guano was a stronger emitter for CH₄ and CO₂ while ornithogenic soil was a stronger emitter for N₂O during FTCs. CO₂ and CH₄ fluxes had a correlation with total organic carbon (TOC) and soil/guano moisture (M_c) in penguin guanos and ornithogenic soils. The specific CO₂–C production rate (CO₂–C/TOC) indicated that the bioavailability of TOC was markedly larger in penguin guanos than in ornithogenic soils during FTCs. This study showed that FTC-released organic C and N from sea animal excreta may play a significant role in FTC-related GHG emissions, which may account for a large proportion of annual fluxes from tundra ecosystems in coastal Antarctica.     

Spatiotemporal variations of nitrous oxide (N2O) emissions from two reservoirs in SW China

Greenhouse gas emissions from hydroelectric dams have recently given rise to controversies about whether hydropower still provides clean energy. China has a large number of dams used for energy supply and irrigation, but few studies have been carried out on aquatic nitrous oxide (N₂O) variation and its emissions in Chinese river-reservoir systems. In this study, N₂O spatiotemporal variations were investigated monthly in two reservoirs along the Wujiang River, Southwest China, and the emission fluxes of N₂O were estimated. N₂O production in the reservoirs tended to be dominated by nitrification, according to the correlation between N₂O and other parameters. N₂O saturation in the surface water of the Wujiangdu reservoir ranged from 214% to 662%, with an average fluctuation of 388%, while in the Hongjiadu reservoir, it ranged from 201% to 484%, with an average fluctuation of 312%. The dissolved N₂O in both reservoirs was over-saturated with respect to atmospheric equilibrium levels, suggesting that the reservoirs were net sources of N₂O emissions to the atmosphere. The averaged N₂O emission flux in the Wujiangdu reservoir was 0.64 μmol m^?2 h^?1, while it was 0.45 μmol m^?2 h^?1 in the Hongjiadu reservoir, indicating that these two reservoirs had moderate N₂O emission fluxes as compared to other lakes in the world. Downstream water of the dams had quite high levels of N₂O saturation, and the estimated annual N₂O emissions from hydropower generation were 3.60 × 10⁵ and 2.15 × 10⁵ mol N₂O for the Wujiangdu and the Hongjiadu reservoir, respectively. These fluxes were similar to the total N₂O emissions from the reservoir surfaces, suggesting that water released from reservoirs would be another important way for N₂O to diffuse into the atmosphere. It can be concluded that dam construction significantly changes the water environment, especially in terms of nutrient status and physicochemical conditions, which have obvious influences on the N₂O spatiotemporal variations and emissions.     

Variations in methane and nitrous oxide mixing ratios at the southern boundary of a Canadian boreal forest

Diurnal and seasonal variations in methane (CH₄) and nitrous oxide (N₂O) mixing ratios were measured above a boreal aspen stand at the southern boundary of the Canadian boreal forest, about 5 km north of agricultural land. The research was conducted between 16 April and 16 September 1994, in the Prince Albert National Park, Saskatchewan, to better understand patterns of CH₄ and N₂O cycling in boreal ecosystems. The research also presents a method for detecting the long-range transport of trace gases using a micrometeorological, laser-based gas monitoring system. Both CH₄ and N₂O featured diurnal cycles consistent with a pattern of net emission for each trace gas. The CH₄ mixing ratio displayed a seasonal variation that was strongly related to soil temperature, with measured values roughly 30 ppb higher in the late summer than in spring. During the latter half of the experiment, the CH₄ mixing ratios varied with wind direction and suggested areas of higher emission to the northeast and east of the measurement tower. The N₂O fluxes also showed favoured directions, although in this case the highest mixing ratios were measured during the springtime in air masses originating south and southwest of the tower. The high springtime values coincided with spring thaw emissions of N₂O from agricultural fields to the south, and the results suggest that the trace gas analysis system detected the long-range transport of N₂O from the agricultural land. Ammonia and ammonium likewise may be transported to the southern boreal forest from agricultural land, and a future investigation at this site could seek to determine the effect of their long-range transport on the southern boreal forest.     

Effect of influent C/N ratio on N2O emissions from anaerobic/anoxic/oxic biological nitrogen removal processes

The problem of producing strong greenhouse gas of nitrous oxide (N₂O) from biological nitrogen removal (BNR) process in wastewater treatment plants (WWTP) has elicited great concern from various sectors. In this study, three laboratory-scale wastewater treatment systems, with influent C/N ratios of 3.4, 5.4, and 7.5, were set up to study the effect of influent C/N ratio on N₂O generation in anaerobic/anoxic/oxic (A²O) process. Results showed, with the increased influent C/N ratio, N₂O generation from both nitrification and denitrification process was decreased, and the N₂O-N conversion ratio of the process was obviously reduced from 2.23 to 0.05%. Nitrification rate in oxic section was reduced, while denitrification rate in anaerobic and anoxic section was elevated and the removal efficiency of COD, NH₄ ⁺-N, TN, and TP was enhanced in different extent. As the C/N ratio increased from 3.4 to 7.5, activities of three key denitrifying enzymes of nitrate reductase, nitrite reductase, and nitrous oxide reductase were increased. Moreover, microorganism analysis indicated that the relative abundance of ammonium-oxidizing bacteria (AOB) and nitrite-oxidizing bacteria (NOB) were positively correlated with N₂O generation, which was reduced from (8.42 ± 3.65) to (3.61 ± 1.66)% and (10.38 ± 4.12) to (4.67 ± 1.62)%, respectively. NosZ gene copy numbers of the A²O system were increased from (1.19 ± 0.49) × 10⁷ to (2.84 ± 0.54) × 10⁸ copies/g MLSS with the influent C/N ratio elevated from 3.4 to 7.5. Hence, appropriate influent C/N condition of A²O process could optimize the microbial community structure that simultaneously improve treatment efficiency and decrease the N₂O generation.

     

Do lagoons near concentrated animal feeding operations promote nitrous oxide supersaturation?

Animal wastewater lagoons nearby concentrated animal feeding operations (CAFOs) represent the latest tendency in global animal farming, severely impacting the magnitude of greenhouse gas emissions, including nitrous oxide (N₂O). We hypothesized that lagoon wastewater could be supersaturated with N₂O as part of incomplete microbial nitrification/denitrification processes, thereby regulating the N₂O partitioning in the gaseous phase. The objectives of this study were: (i) to investigate the magnitude of dissolved N₂O concentrations in the lagoon; and (ii) to determine the extent to which supersaturation of N₂O occurs in wastewater lagoons. Dissolved N₂O concentrations in the wastewater samples were high, ranging from 0.4 to 40.5 μg N₂O mL⁻¹. Calculated dissolved N₂O concentrations from the experimentally measured partition coefficients were much greater than those typically expected in aquatic systems (<∼0.6 μg N₂O mL⁻¹). Knowledge of the factors controlling the magnitude of N₂O supersaturation could potentially bridge mass balance differences between in situ measurements and global N₂O models.