Incremental CH4 and N2O mitigation benefits consistent with the US Government's SC-CO2 estimates

Benefit–cost analysis can serve as an informative input into the policy-making process, but only to the degree it characterizes the major impacts of the regulation under consideration. Recently, the US, amongst other nations, has begun to use estimates of the social cost of CO₂ (SC-CO₂) to develop analyses that more fully capture the climate change impacts of GHG abatement. The SC-CO₂ represents the aggregate willingness to pay to avoid the damages associated with an additional tonne of CO₂ emissions. In comparison, the social costs of non-CO₂ GHGs have received little attention from researchers and policy analysts, despite their non-negligible climate impact. This article addresses this issue by developing a set of social cost estimates for two highly prevalent non-CO₂ GHGs, methane and nitrous oxide. By extending existing integrated assessment models, it is possible to develop a set of social cost estimates for these gases that are consistent with the SC-CO₂ estimates currently in use by the US federal government.Policy relevanceWithin the benefit–cost analyses that inform the design of major regulations, all Federal agencies within the US Government (USG) use a set of agreed upon SC-CO₂ estimates to value the impact of CO₂ emissions changes. However, the value of changes in non-CO₂ GHG emissions has not been included in USG policy analysis to date. This article addresses that omission by developing a set of social cost estimates for two highly prevalent non-CO₂ GHGs, methane and nitrous oxide. These new estimates are designed to be compatible with the USG SC-CO₂ estimates currently in use and may therefore be directly applied to value emissions changes for these non-CO₂ gases within the benefit–cost analyses used to evaluate future policies.     

影响农田氧化亚氮排放过程的土壤因素

土壤理化特性是影响农田氧化亚氮(N2O)产生和排放的重要因素.作者主要讨论了土壤微生物、土壤质地、土壤中化学物质、土壤温度和土壤pH值等对农田N2O的影响.继续深入研究这些因素对农田N2O排放的综合影响和机理以及与其排放量之间的数量关系应是未来的研究重点.为准确估计区域乃至全球范围的农田N2O排放总量,对农田N2O排放模型中关键土壤参数的确定尤为重要.     

Stratospheric N2O5, CH4, and N2O profiles from IR solar occultation spectra

Stratospheric volume mixing ratio profiles of N₂O₅, CH₄, and N₂O have been retrieved from a set of 0.052 cm^–1 resolution (FWHM) solar occultation spectra recorded at sunrise during a balloon flight from Aire sur l'Adour, France (44° N latitude) on 12 October 1990. The N₂O₅ results have been derived from measurements of the integrated absorption by the 1246 cm^–1 band. Assuming a total intensity of 4.32×10^–17 cm^–1/molecule cm^–2 independent of temperature, the retrieved N₂O₅ volume mixing ratios in ppbv (parts per billion by volume, 10^–9), interpolated to 2 km height spacings, are 1.64±0.49 at 37.5 km, 1.92±0.56 at 35.5 km, 2.06±0.47 at 33.5 km, 1.95±0.42 at 31.5 km, 1.60±0.33 at 29.5 km, 1.26±0.28 at 27.5 km, and 0.85±0.20 at 25.5 km. Error bars indicate the estimated 1- uncertainty including the error in the total band intensity (±20% has been assumed). The retrieved profiles are compared with previous measurements and photochemical model results.Laboratoire associé aux Universités Pierre et Marie Curie et Paris Sud.     

Corrigendum to: Incremental CH4 and N2O mitigation benefits consistent with the U.S. Government's SC-CO2 estimates

The light bulb ban introduced by the EU is used as an example to illustrate how to assess the climate impact of a policy that overlaps with a cap-and-trade scheme. The European Commission estimates that by 2020 the reduction in GHG emissions induced by banning incandescent light bulbs will reach 15 million tons annually. The number is a conservative estimate for the reduction in emissions from lighting if the total residential stock of incandescent light bulbs in 2008 is replaced by more efficient lighting sources. However, it ignores that use-phase and some non-use-phase emissions are covered by the EU Emission Trading Scheme (EU ETS). This drastically reduces the amount of GHG emissions saved.

Policy relevance

Several policies such as the EU-wide ban on incandescent light bulbs, energy efficiency mandates and support mechanisms for renewable energy overlap with the EU ETS. While there are typically several justifications for these policies, a chief reason is the reduction of GHG emissions. However, given that the aggregate emissions of the industries covered are fixed by the EU ETS, the climate change mitigation aspect of these policies is not obvious. Using the light bulb ban as an example, this article illustrates how a focus on non-EU ETS emissions changes the assessment of an intervention in terms of GHG reductions.     

The heterogeneous formation of N2O in air containing NO2, O3 and NH3

In a nighttime system and under relatively dry conditions (about 15 ppm H₂O), the reaction mixture of NO₂, O₃, and NH₃ in purified air turns out to result in the formation of nitrous oxide (N₂O). The experiments were performed in a continuous stirred flow reactor, in the concentration region of 0.02–2 ppm.N₂O is thought to arise through the heterogeneous reaction of gaseous N₂O₅ and absorbed NH₃ at the wall of the reaction vessel % MathType!MTEF!2!1!+-% feaafeart1ev1aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn% hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr% 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqaqpepeea0xe9qqVa0l% b9peea0lb9sq-JfrVkFHe9peea0dXdarVe0Fb9pgea0xa9pue9Fve9% Ffc8meGabaqaciGacaGaaeqabaWaaeaaeaaakeaatCvAUfKttLeary% qr1ngBPrgaiuaacqWFOaakcqWFobGtcqWFibasdaWgaaWcbaGae83m% amdabeaakiab-LcaPmaaBaaaleaacqWFHbqyaeqaaOGaey4kaSIaai% ikaiab-5eaonaaBaaaleaacqWFYaGmaeqaaOGae83ta80aaSbaaSqa% aiab-vda1aqabaGccaGGPaWaaSbaaSqaaiaadEgaaeqaaOGaeyOKH4% Qae8Nta40aaSbaaSqaaiab-jdaYaqabaGccqWFpbWtcqGHRaWkcqWF% ibascqWFobGtcqWFpbWtdaWgaaWcbaGae83mamdabeaakiabgUcaRi% ab-HeainaaBaaaleaacqWFYaGmaeqaaOGae83ta8eaaa!59AC!\[(NH_3 )_a + (N_2 O_5 )_g \to N_2 O + HNO_3 + H_2 O\]In principle, there is competition between this reaction and that of adsorbed H₂O with N₂O₅, resulting in the formation of HNO₃. At high water concentrations (RH>75%), no formation of N₂O was found. Although the rate constant of adsorbed NH₃ with gaseous N₂O₅ is much larger than that of the reaction of adsorbed H₂O with gaseous N₂O₅, the significance of the observed N₂O formation for the outside atmosphere is thought to be dependent on the adsorption properties of H₂O and NH₃ on a surface. A number of NH₃ and H₂O adsorption measurements on several materials are discussed.     

Influence of the surface microlayer on the flux of nonconservative trace gases (CO,H2, CH4, N2O) across the ocean-atmosphere interface

Gas exchange experiments were conducted in the tropical Atlantic Ocean during a ship expedition with FS Meteor using a small rubber raft. The temporal change of the mixing ratios of CO, H₂, CH₄ and N₂O in the headspace of a floating glass box and the concentrations of these gases in the water phase were measured to determine their transfer velocities across the ocean-atmosphere interface. The ocean acted as a sink for these gases when the water was undersaturated with respect to the mixing ratio in the headspace. The transfer velocities were different for the individual gases and showed still large differences even when normalized for diffusivity. Applying the laminar film model, film thicknesses of 20 to 70 m were calculated for the observed flux rates of the different gas species. When the water was supersaturated with respect to atmospheric CO, H₂, CH₄ and N₂O, the transfer velocities of the emission process were smaller than those determined for the deposition process. In case of H₂ and CH₄, emission was even not calculable although, based on the observed gradient, the laminar film model predicted significant fluxes at the air-sea interface. The results are interpreted by destruction processes active within the surface microlayer.     

A Note on an improved expression for the atmospheric CO2, N2O,CH4 and O2 integral transmission function: Research note

Abstract

A new analytical expression for the integral transmission function corresponding to the uniformly mixed atmospheric gases (CO₂, N₂O, CH4 and O₂) is proposed for solar radiation models. The expression is based on the latest known spectral absorption data of the gases as well as on the Ñeckel and Labs (1981) extraterrestrial solar spectrum, which is the best currently available. The proposed formula is compared with the known expressions for the integral transmission function of the uniformly mixed gases and the results of this comparison are discussed.     

N2O measurements of air extracted from antarctic ice cores: Implication on atmospheric N2O back to the last glacial-interglacial transition

A method has been developed for determining the N₂O concentrations of air bubbles trapped in ice cores. The air is removed by cutting ice samples of about 45 cm³ with a rotating knife, under pure nitrogen. About 2 cm³ of the gas extracted from the ice is analyzed. The N₂O concentrations are measured by gas chromatography, using electron capture detection with a detection limit of approximately 1 ppbv. The accuracy of the analysis is lower than 6%.This method has been used to analyze 34 Antarctic ice samples. Twelve air samples are from the D57 core and date approximately from AD 1600 and 1900. Data indicate a concentration of about 270 ppbv approximately 400 years ago, and of about 293 ppbv for the beginning of the 20th Century. The other samples have been taken from the Dome C core and date back to the time period extending from the Holocene to the Last Glacial Maximum. The results obtained for the Holocene period are in very good agreement with the concentrations measured for the pre-industrial time from the D57 core and indicate that, during the Holocene period, atmospheric N₂O mixing ratios may have remained fairly constant. The value observed during the last climatic transition suggest a slight increase in the N₂O concentrations when the climate was warming up. The results obtained on samples formed during the Last Glacial Maximum show high scattering which is best explained by the bad quality of this part of the core.     

N2O emissions of India: an assessment of temporal, regional and sector trends

This paper estimates the national level trend of India’s N₂O emissions from 1985–2005 and detailed sub-regional (594 districts) level and sector emissions for the year 2005. N₂O emissions are estimated using the latest methodologies (IPCC 2006), disaggregated activity data and indigenized emission factors. The estimates show that India’s N₂O emissions have grown from 144?Gg in 1985 to 267?Gg in 2005 exhibiting a compounded annual growth rate of 3.1%, which has been gradually declining from 4.7% over 1985–1990 to 2.4% over 2000–2005. N-fertilizer application contributed most to N₂O emissions, a 49% share in 2005 compared to 40% in 1985. Sub-regional (district-level) distribution of N₂O emissions showed rising mean and spread over the years, with average emissions per districts increasing from 305?ton N₂O per year in 1990 to 450?tons in 2005. The main reason being increased use of N-fertilizer. However crop selection plays an important role in N₂O emissions and there are crops providing high economic returns but low N-fertilizer requirements. Agriculture sector could contribute considerably to GDP even with very low N₂O emissions. Indian agriculture practices vary widely in input applications and crop yields across states. The gradual transition from traditional to modern agriculture over past two decades has enhanced the intensity of inputs like N-fertilizer. A simple correlation based on 1985–2005 trends shows that, ceteris paribus, a 10% increase in total crop production is accompanied with a 12.4% increase in N-fertilizer application and a 9.7% increase in total N₂O emissions from India.     

Photochemistry of N2O4 Adsorbed on Ice Surfaces at 193 nm

A multi-layer deposited ice film was prepared through water vapor deposition on a Ni plate in a vacuum chamber at 90 K, and was used as it was or after annealing at 140 K. NO₂ was adsorbed as N₂O₄ approximately 90 K on the ice film prepared as above, and irradiated by 193 nm excimer laser light. The time-of-flight (TOF) spectra of the desorbed species, i.e., NO₂, NO, O₂ and O, were measured by a quadrupole mass spectrometer. The photochemical process obeyed an one-photon process. The relative yields of the products and their TOF spectra were dependent on the preparation condition of the ice film and also varied with the continuation of the laser irradiation. From the ice film annealed at 140 K, NO₂, NO and O₂ were desorbed with an approximate ratio of 1:1:0.01. From the non-annealed film, the relative yield of NO₂ was much smaller than that of NO. The TOF spectrum of NO from the non-annealed ice film consisted of distinctly different two components corresponding to the 1700 and 100 K translational temperature, respectively. The fast component was lost when additional ice was deposited on the adsorbed N₂O₄. NO was supposed to be a predissociation product from the electronically excited NO₂ prepared through the photodissociation of N₂O₄.     

Production of N2O,CH4, and CO2 from soils in the tropical savanna during the dry season

Emissions of N₂O, CH₄, and CO₂ from soils at two sites in the tropical savanna of central Venezuela were determined during the dry season in February 1987. Measured arithmetic mean fluxes of N₂O, CH₄, and CO₂ from undisturbed soil plots to the atmosphere were 2.5×10⁹, 4.3×10¹⁰, and 3.0×10¹³ molecules cm^-2 s^-1, respectively. These fluxes were not significantly affected by burning the grass layer. Emissions of N₂O increased fourfold after simulated rainfall, suggesting that production of N₂O in savanna soils during the rainy season may be an important source for atmospheric N₂O. The CH₄ flux measurements indicate that these savanna soils were not a sink, but a small source, for atmospheric methane. Fluxes of CO₂ from savanna soils increased ninefold two hours after simulated rainfall, and remained three times higher than normal after 16 hours. More research is needed to clarify the significance of savannas in the global cycles of N₂O, CH₄, CO₂, and other trace gases, especially during the rainy season.     

我国瓦里关山、兴隆温室气体CO2、CH4和N2O的背景浓度

为了研究中国大陆温室性气体CO₂、CH₄和N₂O大气浓度的区域分布和变化特征以及与人类活动的关系,从1995~2000年,先后在青海瓦里关山全球大气基准站（36°18′N,100°54′E,3810 m）及河北中国科学院兴隆天文台（40°24′N,117°30′E, 940 m）,利用不锈钢瓶取样和气相色谱法分析,观测了两地大气中温室气体CO₂、CH₄和N₂O的浓度及其变化情况。结果表明:兴隆和瓦里关山站CO₂、CH₄和N₂O的同期年平均浓度分别为376.7×10-6和373.5×10-6,1886×10-9和1831×10-9,316.7×10-9和314.9×10-9。从1995~2000年,兴隆站CO₂、CH₄和N₂O的年增长率分别为1.95×10-6,9.02×10-9和0.75×10-9。而瓦里关山站从1997~2000年,CO₂、CH₄和N₂O的年增长率分别为1.41×10-6,9.95×10-9和0.82×10-9。两地大气中三种气体的浓度与年增长率与全球同类台站的观测结果接近。同时也在一定程度上反映了各自不同的环境背景特征。     

Measurements of N2O photolysis coefficients in the stratosphere: Comparison with model calculations

A balloon-borne continuous actinometer has been developed which measures stratospheric N₂O photolysis coefficients, % MathType!MTEF!2!1!+-% feaafiart1ev1aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn% hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr% 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq-Jc9% vqaqpepm0xbba9pwe9Q8fs0-yqaqpepae9pg0FirpepeKkFr0xfr-x% fr-xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGcbaGaamOAamaaBa% aaleaacaGGobWaaSbaaWqaaiaaikdaaeqaaSGaci4taiabg2da9iab% gkHiTiGacsgaciGGSbGaaiOBaiaacIcaciGGobWaaSbaaWqaaiaaik% daaeqaaSGaci4taiGacMcacaGGVaGaciizaiaadshaaeqaaaaa!44F2!\[j_{N_2 \operatorname{O} = - \operatorname{d} \ln (\operatorname{N} _2 \operatorname{O} )/\operatorname{d} t} \], with a time resolution of approximately 100 s, and a lower detection limit approaching 10^-10 s^-1. The instrument performed successfully, or was at least partially successful, on five stratospheric balloon flights between October 1982 and September 1986. The experimental profiles are compared with model calculations of % MathType!MTEF!2!1!+-% feaafiart1ev1aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn% hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr% 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq-Jc9% vqaqpepm0xbba9pwe9Q8fs0-yqaqpepae9pg0FirpepeKkFr0xfr-x% fr-xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGcbaGaamOAamaaBa% aaleaacaGGobWaaSbaaWqaaiaaikdaaeqaaSGaci4taaqabaaaaa!39A3!\[j_{N_2 \operatorname{O} } \]. The model takes full account of the sphericity of the atmosphere and of the specific flight conditions, but neglects scattering, which should have a negligible effect on % MathType!MTEF!2!1!+-% feaafiart1ev1aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn% hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr% 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq-Jc9% vqaqpepm0xbba9pwe9Q8fs0-yqaqpepae9pg0FirpepeKkFr0xfr-x% fr-xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGcbaGaamOAamaaBa% aaleaacaGGobWaaSbaaWqaaiaaikdaaeqaaSGaci4taaqabaaaaa!39A3!\[j_{N_2 \operatorname{O} } \]. The quantitative results, particularly the altitude and solar zenith angle dependences under extreme conditions, support the low absorption cross-sections of oxygen in the Herzberg continuum as recommended by WMO in 1986 and are inconsistent with Ackerman's tabulations of 1971. It is shown that the altitude dependence of Brewer and Wilson's historical irradiance measurements in the stratospheric window region is well reproduced by our model, but should be multiplied by a factor of 1.75.     

大气CO2浓度升高和秸秆还田对稻麦轮作农田N2O排放的影响

随着大气CO2浓度的逐渐升高,CO2的施肥效应很可能对陆地生态系统的N2O地气交换过程产生一定的影响。在江苏北部的中国稻麦轮作FACE (Free-Air Carbon Dioxide Enrichment) 实验平台上,采用静态箱暗箱-色谱法,研究了一个稻麦轮作周期（2005年6月中旬至2006年6月中旬）3种小麦秸秆还田水平处理(全还田、半还田和不还田)和CO2浓度升高200 μmol·mol-1对稻麦轮作农田N2O排放的影响。结果表明,就当地传统农田管理方式下的砂性土壤稻麦轮作农田N2O排放而言,所采用的观测方法未能检测到显著的秸秆还田效应和大气CO2浓度升高效应。     

Stubble height effects on seasonal microclimate,water balance,and plant development of no-till winter wheat

To investigate some of the effects of standing stubble on microclimate and on the energy and water balance in relation to plant development, winter wheat (Triticum aestivum L.) was seeded directly into spring wheat stubble of three heights: 0 (bare), 15–19, and 30–35 cm. The soil near Sidney, Montana was Williams loam (fine-loamy mixed, frigid family of Typic Argiborolls) a bench mark soil for dryland cropping in the northern Great Plains of the U.S.A. Total wind passage at 9 cm above ground level was 1.5 and 5 times greater over bare as compared with that over short and tall stubble, respectively. Snow accumulation after a late winter storm was 2 and 4 times greater on short and tall stubble treatments, respectively, than on the bare plots. The first overwinter soil recharge was 3 cm more on both stubble treatments, a difference that persisted throughout the growing season. The second overwinter recharge was ca. 1.5 and 4 cm more on short and tall treatments, respectively. Midday net radiation was as much as 15% higher over the bare treatment in the fall and varied from 5 to 11% lower over the bare treatment in the spring, as compared with that over stubble. Stubble albedo was as much as 1.5 times greater than bare albedo in the fall; differences in the spring were small. On heating days, maximum soil surface temperatures were as much as 10°C higher on bare as compared with stubble treatments and soil heat flow as much as 30% greater on bare as compared with stubble treatments; on freezing days, heat flow differences were small.     

The effect of ozone photochemistry on atmospheric and surface temperature changes due to increased CO2, N2O,CH4 and volcanic aerosols in the atmosphere

Abstract

A coupled 1‐D radiative‐convective and photochemical diffusion model is used to study the influence of ozone photochemistry on changes in the vertical temperature structure and surface climate resulting from the doubling of atmospheric CO₂, N₂O, CH₄ and increased stratospheric aerosols owing to the El Chichón volcanic eruption. It is found when CO₂ alone is doubled, that the total ozone column increases by nearly 6% and the resulting increase in the solar heating contributes a smaller temperature decrease in the stratosphere (up to 4 K near the stratopause level). When the concentration of CO₂, N₂O and CH₄ are simultaneously doubled, the total ozone column amount increases by only 2.5% resulting in a reduced temperature recovery in the stratosphere. Additional results concerning the effect of the interaction of ozone photochemistry with the stratospheric aerosol cloud produced by the El Chichón eruption show that it leads to a reduction in stratospheric ozone, which in turn has the effect of increasing the cooling at the surface and above the cloud centre while causing a slight warming below in the lower stratosphere.     

The Cost of Using Global Warming Potentials: Analysing the Trade off Between CO2, CH4 and N2O

The metric governing the trade-off between different greenhouse gases in the Kyoto Protocol, the Global Warming Potentials (GWPs), has received ample critique from both scientific and economic points of view. Here we use an integrated climate-economic optimization model to estimate the cost-effective trade-off between CO₂, CH₄ and N₂O when meeting a temperature stabilization target. We then estimate the increased cost from using GWPs when meeting the same temperature target. Although the efficient valuation of the gases differs significantly from their respective GWPs, the potential economic benefit of valuing them in a more correct way amounts to 3.8 percent of the overall costs of meeting the temperature stabilization target in the base case. In absolute value, this corresponds to an additional net present value cost of US$₂₀₀₀100 billion. To corroborate our findings we perform a Monte Carlo-analysis where several key parameters are randomly varied simultaneously. The result from this exercise shows that our main result is robust to a wide range of changes in the key parameter values, giving a median economic loss from using GWPs of 4.2 percent.     

The Potential Influence of ClO·O2 on Stratospheric Ozone Depletion Chemistry

The inability to explain the observedoxygen suppression of chlorine photosensitized ozoneloss remains a gap in our understanding of thephotochemistry responsible for depletion of thestratospheric ozone layer. It has been suggested thatthe presence of a weakly bound ClO·O₂complexcould explain this effect. The existence of thiscomplex would alter the chlorine budget of thestratosphere, perhaps reducing the chlorine availablefor catalytic ozone destruction. On the other hand,the chemistry of ClO·O₂ provides two newpathwaysfor ClO dimer formation, which could increase the rateof catalytic ozone loss. In this paper, we constrainthe kinetic rate system of ClO·O₂ tomatch themeasured Cl_y budget. It is shown thatClO·O₂cannot be both fairly stable and rapidly form the ClOdimer, or the resulting partitioning of chlorinebecomes incompatible with observations of both ClO andtotal available chlorine. These constraints allow thateither: (1) the ClO·O₂ is fairly stable,but doesnot significantly enhance ClO dimer formation andtherefore has a negligible effect on ozone loss rates,or (2) the ClO·O₂ complex is only veryweaklystable, but does rapidly form the ClO dimer, andtherefore can influence stratospheric ozone depletion.Even at the ClO·O₂ mixing ratios allowedunderthe assumption of weak stability, 0.1 to 0.2 ppbv,significant ozone loss rate enhancements werecalculated. Of course, the chlorine budget constraintalso allows for a thirdpossibility; that ClO·O₂ is neither verystablenor forms Cl₂O₂ very rapidly. Measuredlimits on the reaction rates for ClO·O₂to form the ClO dimer would greatly aid the resolution of thisissue. Since the uncertainties aboutClO·O₂chemistry are so large, a potential role forClO·O₂ in stratospheric ozone loss cannotbe ruled out at this time.     

华东稻麦轮作农田CH4、N2O和NO排放特征

利用同步自动观测系统对华东稻麦轮作农田的CH4、N2O和NO排放进行了长期连续观测,分析了这3种气体排放的季节特征及决定因素,结果表明,华东稻麦轮作农田的CH4、N2O和NO排放具有完全不同的季节变化形式。CH4的排放发生在水稻生长期,其他阶段排放不明显,土壤水分状况是决定整个轮作周期内CH4排放变化的主要因素。N2O排放具有"冬季无,水田少,旱地多"的季节变化特点,尤其以旱地阶段的排放为主,土壤水分状况和温度共同决定着N2O排放的季节变化形式。NO排放具有"冬季无,水田很少,春季旱地多于秋季旱地"的季节分布特点,轮作周期内97.3%±0.6%的NO排放都发生在除冬季以外的旱地阶段,NO排放的季节变化形式由土壤水分状况和温度共同决定。大多数情况下稻田CH4和N2O排放呈互为消长的关系,但在烤田期间,二者却有时甚至同时出现高排放。在N2O日平均排放通量小于5 mg.m-2.h-1时,稻麦轮作农田的N2O和NO排放呈明显的互为消长关系,但大于5 mg.m-2.h-1时,N2O排放很强,同时NO排放也很强。