Odor Threshold Measurement by Dynamic Olfactometry: Significant Operational Variables

Abstract

Combustion flue gases of three different industrial boilers firing miscellaneous fuels were monitored for a twoweek period. Nitric oxide (NO), sulfur dioxide (SO₂), carbon monoxide (CO), carbon dioxide (CO₂), and total hydrocarbons (CxHy) were continuously measured using single-component gas analyzers in parallel with a lowresolution Fourier Transform Infrared (FTIR) gas analyzer. Hydrogen chloride (HCl) was measured continuously using the FTIR analyzer and semi-continuously using a traditional liquid-absorption technique. Nitrous oxide (N₂O), nitrogen dioxide (NO₂), and water vapor (H₂O) were continuously measured using the FTIR analyzer only. Laboratory tests were conducted prior to the field measurements to assess the detection limits of the different measurement methods for each gas component. No significant differences were found between the results of the low-resolution FTIR analyzer and the single-component analyzers or the liquid absorption method.     

Regional and sectoral assessment of greenhouse gas emissions in India

In this paper the authors have estimated for 1990 and 1995 the inventory of greenhouse gases CO₂, CH₄ and N₂O for India at a national and sub-regional district level. The district level estimates are important for improving the national inventories as well as for developing sound mitigation strategies at manageable smaller scales. Our estimates indicate that the total CO₂, CH₄ and N₂O emissions from India were 592.5, 17, 0.2 and 778, 18, 0.3 Tg in 1990 and 1995, respectively. The compounded annual growth rate (CAGR) of these gases over this period were 6.3, 1.2 and 3.3%, respectively. The districts have been ranked according to their order of emissions and the relatively large emitters are termed as hotspots. A direct correlation between coal consumption and districts with high CO₂ emission was observed. CO₂ emission from the largest 10% emitters increased by 8.1% in 1995 with respect to 1990 and emissions from rest of the districts decreased over the same period, thereby indicating a skewed primary energy consumption pattern for the country. Livestock followed by rice cultivation were the dominant CH₄ emitting sources. The waste sector though a large CH₄ emitter in the developed countries, only contributed about 10% the total CH₄ emission from all sources as most of the waste generated in India is allowed to decompose aerobically. N₂O emissions from the use of nitrogen fertilizer were maximum in both the years (more than 60% of the total N₂O). High emission intensities, in terms of CO₂ equivalent, are in districts of Gangetic plains, delta areas, and the southern part of the country. These overlap with districts with large coal mines, mega power plants, intensive paddy cultivation and high fertilizer use. The study indicates that the 25 highest emitting districts account for more than 37% of all India CO₂ equivalent GHG emissions. Electric power generation has emerged as the dominant source of GHG emissions, followed by emissions from steel and cement plants. It is therefore suggested, to target for GHG mitigation, the 40 largest coal-based thermal plants, five largest steel plants and 15 largest cement plants in India as the first step.     

Continuous Infrared Analysis of N2O in Combustion Products

Nitrous oxide (N₂O) levels in the atmosphere are increasing, potentially contributing to the greenhouse effect and depletion of stratospheric ozone. From a limited data base, combustion sources have been identified as a major anthropogenic source of N₂O. However, the existing data base (obtained by traditional grab sampling techniques followed by gas chromatographic analysis) is in question due to the discovery of a sampling artifact. A continuous on-line N₂O analyzer would enable and facilitate the accurate characterization of combustion sources over a range of operating conditions, and also aid in the development of an appropriate sampling technique. This paper addresses the development of a continuous measurement technique, and the evaluation and initial use of a field prototype continuous N₂O analyzer developed at the UCI Combustion Laboratory in cooperation with a major instrument manufacturer. The analyzer is capable of measuring N₂O levels down to a few ppm. The analyzer has been evaluated and used to study the N₂O emissions from a pulverized coal-fired boiler. The N₂O levels found with the analyzer are substantially lower than levels previously attributed to such sources. Initial N₂O measurements made with the analyzer suggest that N₂O levels are not a substantial fraction of the NO_X levels, as previously suggested.     

Nitrous Oxide Emissions from Drained,Cultivated Organic Soils of South Florida

Due to the intense microbial oxidation of organic soils in the Florida Everglades, approximately 1400 kg N/ha are mineralized annually. Most of this nitrogen is lost to the atmosphere through denitrification in the soil. Nitrous oxide is one of the gaseous products of denitrification, therefore the objectives of this study were to determine the quantities of N₂O emitted from these soils and to measure the effect of this N₂O on ambient mixing ratios in the Everglades. Nitrous oxide fluxes from these soils ranged from 4 g N/ha/day, during dry periods, to 4500 g N/ha/day following rainfall events. Nitrous oxide emissions increased with increasing soil moisture. From April through the end of December 1979, a total of 165, 97, and 48 kg N₂O-N/ha were emitted from fallow, St. Augustine grass, and sugarcane fields, respectively. There was a diurnal variation in the N2O mixing ratios of air 8 m above the soil in the Everglades. This diurnal fluctuation was affected by wind speed. There was a significant linear correlation between the average daily mixing ratio and the flux of N₂O from the soil.     

Assessing the uncertainty associated with national greenhouse gas emission inventories:: a case study for Austria

The uncertainty associated with the Austrian Greenhouse Gas emission inventory has been determined for the gases CO₂, CH₄ and N₂O and for the overall greenhouse potential. Expert interviews were conducted to obtain uncertainties in inventory input data. Based on these interviews, error distributions were developed and combined using Monte-Carlo analysis. Results for all sources and gases combined indicate an overall uncertainty between 10.5% and 12% depending on the base year considered. Excluding emissions and the uncertainty associated with forest sinks and natural sources, overall uncertainty decreased by 2% points. The mere ‘random error’, which is considered the level of uncertainty to be achieved with the current methodology (excluding all systematic errors) is 5% points lower. Detailed evaluation shows that much of the overall uncertainty derives from a lack of understanding the processes associated with N₂O emissions from soils. Other important contributors to GHG emission uncertainties are CH₄ from landfills and forests as CO₂ sinks. The uncertainty of the trend has been determined at near 5% points, with solid waste production (landfills) having the strongest contribution. Theoretical considerations do not permit a decrease of the trend uncertainty—even when forest sinks are not considered—below 3% points.     

城市污水污泥处置方式的温室气体排放比较分析

针对我国现在主流的城市污水污泥处置方法:填埋,焚烧,堆肥。用IPCC中推荐的方法和缺省值,对处置过程中产生的温室气体的直接排放、间接排放和替代排放做了计算和分析。填埋过程计算排放的温室气体有CH4,焚烧过程计算排放的有温室气体CO2和N2O,堆肥过程计算的排放的有温室气体CO2和N2O,最终比较的结果都折算成CO2的排放。结果表明,污泥填埋、焚烧、堆肥所产生的CO2的净排放量分别为695.847 kg CO2/t、443.643 kg CO2/t、511.817 kgCO2/t。由于考虑了堆肥以后的有机肥利用,从减排以及污泥资源化的角度分析,得出堆肥是相对好的污泥处置方式。     

Estimating and comparing greenhouse gas emissions with their uncertainties using different methods: A case study for an energy supply utility

Energy supply utilities release significant amounts of greenhouse gases (GHGs) into the atmosphere. It is essential to accurately estimate GHG emissions with their uncertainties, for reducing GHG emissions and mitigating climate change. GHG emissions can be calculated by an activity-based method (i.e., fuel consumption) and continuous emission measurement (CEM). In this study, GHG emissions such as CO₂, CH₄, and N₂O are estimated for a heat generation utility, which uses bituminous coal as fuel, by applying both the activity-based method and CEM. CO₂ emissions by the activity-based method are 12–19% less than that by the CEM, while N₂O and CH₄ emissions by the activity-based method are two orders of magnitude and 60% less than those by the CEM, respectively. Comparing GHG emissions (as CO₂ equivalent) from both methods, total GHG emissions by the activity-based methods are 12–27% lower than that by the CEM, as CO₂ and N₂O emissions are lower than those by the CEM. Results from uncertainty estimation show that uncertainties in the GHG emissions by the activity-based methods range from 3.4% to about 20%, from 67% to 900%, and from about 70% to about 200% for CO₂, N₂O, and CH₄, respectively, while uncertainties in the GHG emissions by the CEM range from 4% to 4.5%. For the activity-based methods, an uncertainty in the Intergovernmental Panel on Climate Change (IPCC) default net calorific value (NCV) is the major uncertainty contributor to CO₂ emissions, while an uncertainty in the IPCC default emission factor is the major uncertainty contributor to CH₄ and N₂O emissions. For the CEM, an uncertainty in volumetric flow measurement, especially for the distribution of the volumetric flow rate in a stack, is the major uncertainty contributor to all GHG emissions, while uncertainties in concentration measurements contribute a little to uncertainties in the GHG emissions.

Implications:Energy supply utilities contribute a significant portion of the global greenhouse gas (GHG) emissions. It is important to accurately estimate GHG emissions with their uncertainties for reducing GHG emissions and mitigating climate change. GHG emissions can be estimated by an activity-based method and by continuous emission measurement (CEM), yet little study has been done to calculate GHG emissions with uncertainty analysis. This study estimates GHG emissions and their uncertainties, and also identifies major uncertainty contributors for each method.     

Influence of operating conditions on nitrous oxide formation during nitritation and nitrification

Nitrous oxide (N₂O), a strong greenhouse gas, can be produced by ammonium-oxidizing bacteria (AOB) as a by-product of ammonium oxidation and can potentially be formed in all types of nitrification processes. However, partial nitritation has been reported to cause significantly higher N₂O emissions than complete nitrification. In the study presented here, the mechanisms and factors that drive N₂O formation by AOB were investigated with respect to different operational strategies to achieve nitrite accumulation base on combined evaluation of oxygen uptake rate (OUR) and N₂O formation rate. On the one hand, N₂O formation during partial nitritation and nitrification in a continuously stirred tank reactor (CSTR) with continuous aerobic conditions was observed. On the other hand, the effect of intermittent aeration on N₂O formation during nitrification was investigated. The presence of nitrite, the extend of sludge-specific ammonium loading, low oxygen concentration, and transition from aerobic to anoxic conditions significantly increased N₂O formation in this reactor independently from each other, indicating that different formation pathways, supposedly via nitrite or hydroxylamine, were active.     

Short-term effect of increasing nitrogen deposition on CO2, CH4 and N2O fluxes in an alpine meadow on the Qinghai-Tibetan Plateau,China

An increasing nitrogen deposition experiment (2 g N m^?2 year^?1) was initiated in an alpine meadow on the Qinghai-Tibetan Plateau in May 2007. The greenhouse gases (GHGs), including CO₂, CH₄ and N₂O, was observed in the growing season (from May to September) of 2008 using static chamber and gas chromatography techniques. The CO₂ emission and CH₄ uptake rate showed a seasonal fluctuation, reaching the maximum in the middle of July. We found soil temperature and water-filled pore space (WFPS) were the dominant factors that controlled seasonal variation of CO₂ and CH₄ respectively and lacks of correlation between N₂O fluxes and environmental variables. The temperature sensitivity (Q₁₀) of CO₂ emission and CH₄ uptake were relatively higher (3.79 for CO₂, 3.29 for CH₄) than that of warmer region ecosystems, indicating the increase of temperature in the future will exert great impacts on CO₂ emission and CH₄ uptake in the alpine meadow. In the entire growing season, nitrogen deposition tended to increase N₂O emission, to reduce CH₄ uptake and to decrease CO₂ emission, and the differences caused by nitrogen deposition were all not significant (p < 0.05). However, we still found significant difference (p < 0.05) between the control and nitrogen deposition treatment at some observation dates for CH₄ rather than for CO₂ and N₂O, implying CH₄ is most susceptible in response to increased nitrogen availability among the three greenhouse gases. In addition, we found short-term nitrogen deposition treatment had very limited impacts on net global warming potential (GWP) of the three GHGs together in term of CO₂-equivalents. Overall, the research suggests that longer study periods are needed to verify the cumulative effects of increasing nitrogen deposition on GHG fluxes in the alpine meadow.     

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.     

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.     

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.     

Nitrous oxide emissions from an intensively managed greenhouse vegetable cropping system in Northern China

Nitrous oxide (N₂O) emissions from a typical greenhouse vegetable system in Northern China were measured from February 2004 to January 2006 using a close chamber method. Four nitrogen management levels (NN, MN, CN, and SN) were used. N₂O emissions occurred intermittently in the growing season, strongly correlating with N fertilization and irrigation. No peak emissions were observed after fertilization in the late Autumn season due to low soil temperature. 57-94% of the seasonal N₂O emissions came from the initial growth stage, corresponding to the rewetting process in the soil. The annual N₂O emissions ranged from 2.6 to 8.8 kg N ha⁻¹ yr⁻¹, accounting for 0.27-0.30% of the annual nitrogen input. Compared with conventional N management, site-specific N management reduced N fertilization rate by 69% in 2004 and by 76% in 2005, and consequently reduced N₂O emissions by 51% in 2004 and 27% in 2005, respectively.     

Effect of biochar on nitrous oxide emission and its potential mechanisms

Extensive use of biochar to mitigate nitrous oxide (N₂O) emission is limited by the lack of understanding on the exact mechanisms altering N₂O emission from biochar-amended soil. Biochars produced from rice straw and dairy manure at 350 and 500 °C by oxygen-limited pyrolysis were used to investigate their influence on N₂O emission. A quadratic effect of biochar levels was observed on the N₂O emissions. The potential mechanisms were explored by terminal restriction fragment length polymorphism (T-RFLP) and real-time polymerase chain reaction (qPCR). A lower relative abundance of bacteria, which included ammonia-oxidizing bacteria (AOB) and nitrite-oxidizing bacteria (NOB), was observed at 4% biochar application rate. Reduced copy numbers of the ammonia monooxygenase gene amoA and the nitrite reductase gene nirS coincided with decreased N₂O emissions. Therefore, biochar may potentially alter N₂O emission by affecting ammonia-oxidizing and denitrification bacteria, which is determined by the application rate of biochar in soil.

Implications:Biochar research has received increased interest in recent years because of the potential beneficial effects of biochar on soil properties. Recent research shows that biochar can alter the rates of nitrogen cycling in soil systems by influencing nitrification and denitrification, which are key sources of the greenhouse gas nitrous oxide (N₂O). However, there are still some controversial data. The purpose of this research was to (1) examine how applications of different dose of biochar to soil affect emission of N₂O and (2) improve the understanding of the underlying mechanisms.     

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.     

A2O工艺中N2O的产生与逸散特征简

目前污水处理过程中产生温室气体的问题已经引起普遍关注。本文通过实验室小试,研究了不同污水水质条件下A²O工艺中N₂O的产生特征,以及氧化亚氮还原酶编码基因nosZ含量对N₂O产生量的影响。结果表明,在A²O工艺中的各单元均有N₂O产生,其中厌氧池产生量最大,约占总产生量的32%~85%;A²O工艺产生的N₂O主要通过逸散进入大气,少量随二沉池出水进入到环境中。N₂O的产生量与污泥中nosZ的含量成负相关,而碳源和DO对含有nosZ基因的反硝化细菌有明显的影响,低DO环境和充足的碳源能够极大的促进其含量的提高,从而显著减少N₂O的产生量。     

Toward better understanding and feasibility of controlling greenhouse gas emissions from treatment of industrial wastewater with activated sludge

Wastewater treatment plants (WWTPs) have been recognized as important sources for anthropogenic greenhouse gas (GHG) emission. The objective of the study was to thoroughly investigate a typical industrial WWTP in southern Taiwan in winter and summer which possesses the emission factors close to those reported values, with the analyses of emission factors, mass fluxes, fugacity, lab-scale in situ experiments, and impact assessment. The activated sludge was the important source in winter and summer, and nitrous oxide (N₂O) was the main contributor (e.g., 57 to 91 % of total GHG emission in a unit of kg carbon dioxide-equivalent/kg chemical oxygen demand). Albeit important for the GHGs in the atmosphere, the fractional contribution of the GHG emission to the carbon or nitrogen removal in wastewater treatment was negligible (e.g., less than 1.5 %). In comparison with the sludge concentration or retention time, adjusting the aeration rate was more effective to diminish the GHG emission in the activated sludge without significantly affecting the treated water quality. When the aeration rate in the activated sludge simulation was reduced by 75 %, the mass flux of N₂O could be diminished by up to 53 % (from 9.6 to 4.5 mg/m²-day). The total emission in the WWTP (including carbon dioxide, methane, and N₂O) would decrease by 46 % (from 0.67 to 0.36 kg CO₂-equiv/kg COD). However, the more important benefit of changing the aeration rate was lowering the energy consumption in operation of the WWTP, as the fractional contribution of pumping to the total emission from the WWTP ranged from 46 to 93 % within the range of the aeration rate tested. Under the circumstance in which reducing the burden of climate change is a global campaign, the findings provide insight regarding the GHG emission from treatment of industrial wastewater and the associated impact on the treatment performance and possible mitigation strategies by operational modifications.

     

Assessment of nitrogen losses through nitrous oxide from abattoir wastewater-irrigated soils

The land disposal of waste and wastewater is a major source of N₂O emission. This is due to the presence of high concentrations of nitrogen (N) and carbon in the waste. Abattoir wastewater contains 186 mg/L of N and 30.4 mg/L of P. The equivalent of 3 kg of abattoir wastewater-irrigated soil was sieved and taken in a 4-L plastic container. Abattoir wastewater was used for irrigating the plants at the rates of 50 and 100 % field capacity (FC). Four crop species were used with no crop serving as a control. Nitrous oxide emission was monitored using a closed chamber technique. The chamber was placed inside the plastic container, and N₂O emission was measured for 7 days after the planting. A syringe and pre-evacuated vial were used for collecting the gas samples; a fresh and clean syringe was used each time to avoid cross-contamination. The collected gas samples were injected into a gas chromatography device immediately after each sampling to analyse the concentration of N₂O from different treatments. The overall N₂O emission was compared for all the crops under two different abattoir wastewater treatment rates (50 and 100 % FC). Under 100 % FC (wastewater irrigation), among the four species grown in the abattoir wastewater-irrigated soil, Medicago sativa (23 mg/pot), Sinapis alba (21 mg/pot), Zea mays (20 mg/pot) and Helianthus annuus (20 mg/pot) showed higher N₂O emission compared to the 50 % treatments—M. sativa (17 mg/pot), S. alba (17 mg/pot), Z. mays (18 mg/pot) and H. annuus (18 mg/pot). Similarly, pots with plants have shown 15 % less emission than the pots without plants. Similar trends of N₂O emission flux were observed between the irrigation period (4-week period) for 50 % FC and 100 % FC. Under the 100 % FC loading rate treatments, the highest N₂O emission was in the following order: week 1 > week 4 > week 3 > week 2. On the other hand, under the 50 % FC loading rate treatments, the highest N₂O emission was recorded in the first few weeks and in the following order: week 1 > week 2 > week 3 > week > 4. Since N₂O is a greenhouse gas with high global warming potential, its emission from wastewater irrigation is likely to impact global climate change. Therefore, it is important to examine the effects of abattoir wastewater irrigation on soil for N₂O emission potential.

     

Differentiation of nitrous oxide emission factors for agricultural soils

Nitrous oxide (N₂O) direct soil emissions from agriculture are often estimated using the default IPCC emission factor (EF) of 1%. However, a large variation in EFs exists due to differences in environment, crops and management. We developed an approach to determine N₂O EFs that depend on N-input sources and environmental factors. The starting point of the method was a monitoring study in which an EF of 1% was found. The conditions of this experiment were set as the reference from which the effects of 16 sources of N input, three soil types, two land-use types and annual precipitation on the N₂O EF were estimated. The derived EF inference scheme performed on average better than the default IPCC EF. The use of differentiated EFs, including different regional conditions, allows accounting for the effects of more mitigation measures and offers European countries a possibility to use a Tier 2 approach.     

Nitrous oxide emissions from light duty vehicles

Nitrous oxide (N₂O) emissions measurements were made on light duty gasoline and light duty diesel vehicles during chassis dynamometer testing conducted at the Environment Canada and California Air Resources Board vehicle emissions laboratories between 2001 and 2007. Per phase and composite FTP emission rates were measured. A subset of vehicles was also tested using other driving cycles to characterize emissions as a function of different driving conditions. Vehicles were both new (<6500 km) and in-use (6500–160,000 km) and were tested on low sulfur gasoline (<30 ppm) or low sulfur diesel (<300 ppm). Measurements from selected published studies were combined with these new measurements to give a test fleet of 467 vehicles meeting both US EPA and California criteria pollutant emissions standards between Tier 0 and Tier 2 Bin 3 or SULEV. Aggregate distance-based and fuel-based emission factors for N₂O are reported for each emission standard and for each of the different test cycles. Results show that the distinction between light duty automobile and light duty truck is not significant for any of the emission standards represented by the test fleet and the distinction between new and aged catalyst is significant for vehicles meeting all emission standards but Tier 2. This is likely due to the relatively low mileage accumulated by the Tier 2 vehicles in this study as compared to the durability requirement of the standard. The FTP composite N₂O emission factors for gasoline vehicles meeting emission standards more stringent than Tier 1 are substantially lower than those currently used by both Canada and the US for the 2005 inventories. N₂O emission factors from test cycles other than the FTP illustrate the variability of emission factors as a function of driving conditions. N₂O emission factors are shown to strongly correlate with NMHC/NMOG emission standards and less strongly with NO_X and CO emission standards. A review of several published reports on the effect of gasoline sulfur content on N₂O emissions suggests that additional research is needed to adequately quantify the increase in N₂O emissions as a function of fuel sulfur.