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1.
Humans seem to have doubled the global rate of terrestrial nitrogen fixation. Globally 50–70% (85 Tg, 1 Tg=1012 g) of the nitrogen supplied in fertilizer (80 Tg N/a) and leguminous crops (40–80 Tg N/a) are used to feed cattle. The aim of the present study was to derive some estimates of global N2O production from animal manure. As the parameter giving the most stable numerical basis for regional and global extrapolation we adopted the molar emission ratios of N2O to NH3. These ratios were measured in cattle, pig and chicken housings with different manure handling systems, in dung-heaps and in liquid manure storage tanks. Individual molar emission ratios from outside manure piles varied over two orders of magnitude, strongly dependent on the treatment of the manure. A median emission ratio of 1.6×10-2 (n=65) was obtained in cow-sheds with slatted floors and liquid manure stored underneath and a median ratio of 24×10-2 (n=31) was measured in a beef cattle housing with a solid manure handling system.We next extrapolated to global NH3 emissions from those estimated for Europe, using N uptake by the animals as a scaling factor. Multiplication with observed N2O to NH3 ratios next provided some estimates of regional and global N2O emissions. To account for the great variability of the emission ratios of N2O/NH3, we developed upper and lower case emission scenarios, based on lower and upper quartiles of measured emission ratios. The global emission from cattle and swine manure is in the range of 0.2–2.5 Tg N-N2O/a, representing 44+-39% of the annual atmospheric accumulation rate. This N2O emission arises from about 40 Tg N/a of cattle and pig manure stored in or at animal housings. We did not account for N2O emissions from another 50 Tg N/a excreted by grazing cattle, goats and sheep, and application of the manure to agricultural fields. Our study makes it clear that major anthropogenic N2O emissions may well arise from animal manure. The large uncertainty of emission ratios, which we encountered, show that much more intense research efforts are necessary to determine the factors that influence N2O emissions from domestic animal manure both in order to derive a more reliable global estimate of N2O release and to propose alternative waste treatment methods causing smaller N2O releases. In our studies we found large enhancements in N2O releases when straw was added to the manure, which is a rather common practice. In view of the ongoing discussion in Europe to re-install the traditional solid manure system (bed down cattle) for environmental and animal welfare reasons, it is noteworthy that our measurements indicate highest N2O release from this particulary system.In a similar manner, but based on a smaller data set, we also estimated the release of CH4 from cattle and swine manure and from liquid manure only to be about 9 Tg/year in good agreement with the estimate by the Environmental Protection Agency (1994) of 8.6+-2.6 Tg/year. A total annual methane release as high as 34 Tg/a was derived for solid and liquid cattle and pig manure from animals in housings.  相似文献   

2.
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.  相似文献   

3.
CH4和N2O作为主要温室气体,自工业革命以来排放量急剧增加,已经被列入《京都议定书》要求控制它们的排放。本文利用高光谱分辨率的辐射传输模式,计算了CH4、N2O在晴空大气和有云大气条件下的瞬时辐射效率和平流层调整的辐射效率,以及它们的全球增温潜能(GWP)和全球温变潜能(GTP),并根据模式结果拟合了CH4和N2O的辐射强迫的简单计算公式。本文的研究表明:CH4和N2O在有云大气下的平流层调整的辐射效率分别为4.142×10-4 W m-2 ppb-1和3.125×10-3 W m-2 ppb-1 (1ppb=10-9),经大气寿命调整后的辐射效率分别为3.732×10-4 W m-2 ppb-1和2.987×10-3 W m-2 ppb-1,与IPCC(2007)的相应结果高度一致。CH4和N2O 100年的全球增温潜能GWP分别为16和266;100年的脉冲排放的全球温变潜能GTPP分别为0.24和233;持续排放的全球温变潜能GTPS分别为18和268。它们在未来全球变暖和气候变化中,影响仅次于CO2,仍然起着非常关键的作用。  相似文献   

4.
Field measurements of N2O emission rates were carried out from August until October 1982 in a subtropical region in Europe, i.e. in Andalusia, Spain. The measurements were performed by using an automatic sampling and analysis technique allowing the semi-continuous determination of N2O emission rates. The N2O emission rates were positively correlated to the soil surface temperature and exhibited a diurnal rhythm with maximum rates in the afternoon and minimum rates in the early morning with average values of 1 g N2O–N/m2/h for the grass lawn and 15 g N2O–N/m2/h for cultivated land. Application of urea and ammonium nitrate resulted in elevated N2O emission rates when compared to the unfertilized control. The loss of fertilizer-nitrogen as N2O was 0.18% for urea and 0.04% for NH4NO3 which compares very well with data obtained in a temperate climate (Germany). The total source strength of fertilizer-derived N2O is estimated to be 0.01–2.2 Tg N2O–N per year. The N2O flux from unfertilized natural soils may be as high as 4.5 Tg N2O–N, indicating that the N2O emission from soils contributes significantly to the global N2O budget.  相似文献   

5.
During 18–23 July 1990, 31 smoke samples were collected from an aircraft flying at low altitudes through the plumes of tropical savanna fires in the Northern Territory, Australia. The excess (above background) mixing ratios of 17 different trace gases including CO2, CO, CH4, several non-methane hydrocarbons (NMHC), CH3CHO, NO x (– NO + NO2), NH3, N2O, HCN and total unspeciated NMHC and sulphur were measured. Emissionratios relative to excess CO2 and CO, and emissionfactors relative to the fuel carbon, nitrogen or sulphur content are determined for each measured species. The emission ratios and factors determined here for carbon-based gases, NO x , and N2O are in good agreement with those reported from other biomass burning studies. The ammonia data represent the first such measurements from savanna fires, and indicate that NH3 emissions are more than half the strength of NO x emissions. The emissions of NO x , NH3, N2O and HCN together represent only 27% of the volatilised fuel N, and are primarily NO x (16%) and NH3 (9%). Similarly, only 56% of the volatilised fuel S is accounted for by our measurements of total unspeciated sulphur.  相似文献   

6.
A three-dimensional model of the global ammonia cycle   总被引：16，自引：0，他引：16  
Using a three-dimensional (3-D) transport model of the troposphere, we calculated the global distributions of ammonia (NH3) and ammonium (NH 4 + ), taking into account removal of NH3 on acidic aerosols, in liquid water clouds and by reaction with OH. Our estimated global 10°×10° NH3 emission inventory of 45 Tg N-NH3 yr– provides a reasonable agreement between calculated wet NH 4 + deposition and measurements and of measured and modeled NH 4 + in aerosols, although in Africa and Asia especially discrepancies exist.NH3 emissions from natural continental ecosystems were calculated applying a canopy compensation point and oceanic NH3 emissions were related to those of DMS (dimethylsulfide). In many regions of the earth, the pH found in rain and cloud water can be attributed to acidity derived from NO, SO2 and DMS emissions and alkalinity from NH3. In the remote lower troposphere, sulfate aerosols are calculated to be almost neutralized to ammonium sulfate (NH4)2SO4, whereas in the middle and upper troposphere, according to our calculations, the aerosol should be more acidic, as a result of the oxidation of DMS and SO2 throughout the troposphere and removal of NH3 on acidic aerosols at lower heights. Although the removal of NH3 by reaction with the OH radical is relatively slow, the intermediate NH2 radical can provide a substantial annual N2O source of 0.9 –0.4 +0.9 Tg, thus contributing byca. 5% to estimated global N2O production. The oxidation by OH of NH3 from anthropogenic sources accounts for 10% of the estimated total anthropogenic sources of N2O. This source was not accounted for in previous studies, and is mainly located in the tropics, which have high NH3 and OH concentrations. Biomass burning plumes, containing high NO x and NH3 concentrations provide favourable conditions for gas phase N2O production. This source is probably underestimated in this model study, due to the coarse resolution of the 3-D model, and the rather low biomass burning NH3 and NO x emissions adopted. The estimate depends heavily on poorly known concentrations of NH3 (and NO x ) in the tropics, and uncertainties in the rate constants of the reactions NH2 + NO2 N2O + H2O (R4), and NH2 + O3 NH2O + O2 (R7).  相似文献   

7.
An emission pathway for stabilization at 6?Wm?2 radiative forcing   总被引：1，自引：0，他引：1  
Representative Concentration Pathway 6.0 (RCP6) is a pathway that describes trends in long-term, global emissions of greenhouse gases (GHGs), short-lived species, and land-use/land-cover change leading to a stabilisation of radiative forcing at 6.0 Watts per square meter (Wm?2) in the year 2100 without exceeding that value in prior years. Simulated with the Asia-Pacific Integrated Model (AIM), GHG emissions of RCP6 peak around 2060 and then decline through the rest of the century. The energy intensity improvement rates changes from 0.9% per year to 1.5% per year around 2060. Emissions are assumed to be reduced cost-effectively in any period through a global market for emissions permits. The exchange of CO2 between the atmosphere and terrestrial ecosystem through photosynthesis and respiration are estimated with the ecosystem model. The regional emissions, except CO2 and N2O, are downscaled to facilitate transfer to climate models.  相似文献   

8.
The MAGICC (Model for the Assessment of Greenhouse gas Induced Climate Change) model simulation has been carried out for the 2000–2100 period to investigate the impacts of future Indian greenhouse gas emission scenarios on the atmospheric concentrations of carbon dioxide, methane and nitrous oxide besides other parameters like radiative forcing and temperature. For this purpose, the default global GHG (Greenhouse Gases) inventory was modified by incorporation of Indian GHG emission inventories which have been developed using three different approaches namely (a) Business-As-Usual (BAU) approach, (b) Best Case Scenario (BCS) approach and (c) Economy approach (involving the country’s GDP). The model outputs obtained using these modified GHG inventories are compared with various default model scenarios such as A1B, A2, B1, B2 scenarios of AIM (Asia-Pacific Integrated Model) and P50 scenario (median of 35 scenarios given in MAGICC). The differences in the range of output values for the default case scenarios (i.e., using the GHG inventories built into the model) vis-à-vis modified approach which incorporated India-specific emission inventories for AIM and P50 are quite appreciable for most of the modeled parameters. A reduction of 7% and 9% in global carbon dioxide (CO2) emissions has been observed respectively for the years 2050 and 2100. Global methane (CH4) and global nitrous oxide (N2O) emissions indicate a reduction of 13% and 15% respectively for 2100. Correspondingly, global concentrations of CO2, CH4 and N2O are estimated to reduce by about 4%, 4% and 1% respectively. Radiative forcing of CO2, CH4 and N2O indicate reductions of 6%, 14% and 4% respectively for the year 2100. Global annual mean temperature change (incorporating aerosol effects) gets reduced by 4% in 2100. Global annual mean temperature change reduces by 5% in 2100 when aerosol effects have been excluded. In addition to the above, the Indian contributions in global CO2, CH4 and N2O emissions have also been assessed by India Excluded (IE) scenario. Indian contribution in global CO2 emissions was observed in the range of 10%–26%, 6%–36% and 10%–38% respectively for BCS, Economy and BAU approaches, for the years 2020, 2050 and 2100 for P50, A1B-AIM, A2-AIM, B1-AIM & B2-AIM scenarios. CH4 and N2O emissions indicate about 4%–10% and 2%–3% contributions respectively in the global CH4 and N2O emissions for the years 2020, 2050 and 2100. These Indian GHG emissions have significant influence on global GHG concentrations and consequently on climate parameters like RF and ∆T. The study reflects not only the importance of Indian emissions in the global context but also underlines the need of incorporation of country specific GHG emissions in modeling to reduce uncertainties in simulation of climate change parameters.  相似文献   

9.
Biomass burning has important impacts on atmospheric chemistry and climate. Fires in tropical forests and savannas release large quantities of trace gases and particulate matter. Combustion of biofuels for cooking and heating constitutes a less spectacular but similarly widespread biomass burning activity. To provide the groundwork for a quantification of this source, we determined in rural Zimbabwe the emissions of CO2, CO, and NO from more than 100 domestic fires fueled by wood, agricultural residues, and dung. The results indicate that, compared to open savanna fires, emissions from domestic fires are shifted towards products of incomplete combustion. A tentative global analysis shows that the source strength of domestic biomass burning is on the order of 1500 Tg CO2–C yr–1, 140 Tg CO–C yr–1, and 2.5 Tg NO–N yr–1. This represents contributions of about 7 to 20% to the global budget of these gases.  相似文献   

10.
Using a global carbon cycle model (GLOCO) that considers seven terrestrial biomes, surface and deep ocean layers based on the HILDA model and a single mixed atmosphere, we analyzed the response of atmospheric CO2 concentration and oceanic DIC and DOC depth profiles to additions of carbon to the atmosphere and ocean. The rate of transport of carbon to the deepest oceanic layers is rather insensitive to the atmosphereic-ocean surface gas exchange coefficient over a wide range, hence discrepancies between researchers on the precise global average value of this coefficient do not significantly affect predictions of atmospheric response to anthropogenic inputs. Upwelling velocity, on the other hand, amplifies oceanic response by increasing primary production in the upper ocean layers, resulting in a larger flux into DOC and sediments and increased carbon storage; experiments to reduce the uncertainty in this parameter would be valuable.The location of the carbon addition, whether it is released in the atmosphere or in the middle of the oceanic thermocline, has a significant impact on the maximum atmospheric CO2 concentration (pCO2) subsequently reached, suggesting that oceanic burial of a significant fraction of carbon emissions (e.g. via clathrate hydrides) may be an important management option for limiting pCO2 buildup. Our analysis indicates that the effectiveness of ocean burial decreases asymptotically below about 1000 m depth. With a constant emissions scenario (at 1990 levels), pCO2 at year 2100 is reduced from 501 ppmv considering all emissions go to the atmosphere, to 422 ppmv with ocean burial at a depth of 1000 m of 50% of the fossil fuel emissions. An alternative scenario looks at stabilizing pCO2 at 450 ppmv; with no ocean burial of fossil fuel emissions, the rate of emissions has to be cut drastically after the year 2010, whereas oceanic burial of 2 GtC/yr allows for a smoother transition to alternative energy sources.  相似文献   

11.
Agricultural soils are a major source of atmospheric nitrous oxide (N2O), a potent greenhouse gas (GHG). Because N2O emissions strongly depend on soil type, climate, and crop management, their inventory requires the combination of biophysical and economic modeling, to simulate farmers’ behavior. Here, we coupled a biophysical soil-crop model, CERES-EGC, with an economic farm type supply model, AROPAj, at the regional scale in northern France. Response curves of N2O emissions to fertilizer nitrogen (Nf) inputs were generated with CERES-EGC, and linearized to obtain emission factors. The latter ranged from 0.001 to 0.0225 kg N2O-N kg???1 Nf, depending on soil and crop type, compared to the fixed 0.0125 value of the IPCC guidelines. The modeled emission factors were fed into the economic model AROPAj which relates farm-level GHG emissions to production factors. This resulted in a N2O efflux 20% lower than with the default IPCC method. The costs of abating GHG emissions from agriculture were calculated using a first-best tax on GHG emissions, and a second-best tax on their presumed factors (livestock size and fertilizer inputs). The first-best taxation was relatively efficient, achieving an 8% reduction with a tax of 11 €/ t-CO2-equivalent, compared to 68 €/t-CO2 eq for the same target with the second-best scheme.  相似文献   

12.
Strategies for mitigating the increasing concentration of carbon dioxide (CO2) in the atmosphere include sequestering carbon (C) in soils and vegetation of terrestrial ecosystems. Carbon and nitrogen (N) move through terrestrial ecosystems in coupled biogeochemical cycles, and increasing C stocks in soils and vegetation will have an impact on the N cycle. We conducted simulations with a biogeochemical model to evaluate the impact of different cropland management strategies on the coupled cycles of C and N, with special emphasis on C-sequestration and emission of the greenhouse gases methane (CH4) and nitrous oxide (N2O). Reduced tillage, enhanced crop residue incorporation, and farmyard manure application each increased soil C-sequestration, increased N2O emissions, and had little effect on CH4 uptake. Over 20 years, increases in N2O emissions, which were converted into CO2-equivalent emissions with 100-year global warming potential multipliers, offset 75–310% of the carbon sequestered, depending on the scenario. Quantification of these types of biogeochemical interactions must be incorporated into assessment frameworks and trading mechanisms to accurately evaluate the value of agricultural systems in strategies for climate protection.  相似文献   

13.
Effects of tropical deforestation on global and regional atmospheric chemistry   总被引：10，自引：0，他引：10  
A major portion of tropospheric photochemistry occurs in the tropics. Deforestation, colonization, and development of tropical rain forest areas could provoke significant changes in emissions of radiatively and photochemically active trace gases. A brief review of studies on trace-gas emissions in pristine and disturbed tropical habitats is followed by an effort to model regional tropospheric chemistry under undisturbed and polluted conditions. Model results suggest that changing emissions could stimulate photochemistry leading to enhanced ozone production and greater mineral acidity in rainfall in colonized agricultural regions. Model results agree with measurements made during the NASA ABLE missions. Under agricultural/pastoral development scenarios, tropical rain forest regions could export greater levels of N2O, CH4, CO, and photochemical precursors of NO y and O3 to the global atmosphere with implications for climatic warming.  相似文献   

14.
Previous research has demonstrated that soil carbon sequestration through adoption of conservation tillage can be economically profitable depending on the value of a carbon offset in a greenhouse gas (GHG) emissions market. However adoption of conservation tillage also influences two other potentially important factors, changes in soil N2O emissions and CO2 emissions attributed to changes in fuel use. In this article we evaluate the supply of GHG offsets associated with conservation tillage adoption for corn-soy-hay and wheat-pasture systems of the central United States, taking into account not only the amount of carbon sequestration but also the changes in soil N2O emission and CO2 emissions from fuel use in tillage operations. The changes in N2O emissions are derived from a meta-analysis of published studies, and changes in fuel use are based on USDA data. These are used to estimate changes in global warming potential (GWP) associated with adoption of no-till practices, and the changes in GWP are then used in an economic analysis of the potential supply of GHG offsets from the region. Simulation results demonstrate that taking N2O emissions into account could result in substantial underestimation of the potential for GHG mitigation in the central U.S. wheat pasture systems, and large over-estimation in the corn-soy-hay systems. Fuel use also has quantitatively important effects, although generally smaller than N2O. These findings suggest that it is important to incorporate these two effects in estimates of GHG offset potential from agricultural lands, as well as in the design of GHG offset contracts for more complete accounting of the effect that no-till adoption will have on greenhouse gas emissions.  相似文献   

15.
Emission of nitrous oxide from temperate forest soils into the atmosphere   总被引：5，自引：0，他引：5  
N2O emission rates were measured during a 13-month period from July 1981 till August 1982 with a frequency of once every two weeks at six different forest sites in the vicinity of Mainz, Germany. The sites were selected on the basis of soil types typical for many of the Central European forest ecosystems. The individual N2O emission rates showed a high degree of temporal and spatial variabilities which, however, were not significantly correlated to variabilities in soil moisture content or soil temperatures. However, the N2O emission rates followed a general seasonal trend with relatively high values during spring and fall. These maxima coincided with relatively high soil moisture contents, but may also have been influenced by the leaf fall in autumn. In addition, there was a brief episode of relatively high N2O emission rates immediately after thawing of the winter snow. The individual N2O emission rates measured during the whole season ranged between 1 and 92 g N2O-N m–2 h–1. The average values were in the range of 3–11 g N2O-N m–2 h–1 and those with a 50% probability were in the range of 2–8 g N2O-N m–2 h–1. The total source strength of temperate forest soils for atmospheric N2O may be in the range of 0.7–1.5 Tg N yr–1.  相似文献   

16.
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.  相似文献   

17.
This paper provides estimates of emissions of two important but often not well-characterized greenhouse gas (GHG) emissions related to transportation energy use: methane (CH4) and nitrous oxide (N2O). The paper focuses on emissions of CH4 and N2O from motor vehicles because unlike emissions of CO2, which are relatively easy to estimate, emissions of CH4 and N2O are a function of many complex aspects of combustion dynamics and of the type of emission control systems used. They therefore cannot be derived easily and instead must be determined through the use of published emission factors for each combination of fuel, end-use technology, combustion conditions, and emission control system. Furthermore, emissions of CH4 and N2O may be particularly important with regard to the relative CO2-equivalent GHG emissions of the use of alternative transportation fuels, in comparison with the use of conventional fuels. By analyzing a database of emission estimates, we develop emission factors for N2O and CH4 from conventional vehicles, in order to supplement recent EPA and IPCC estimates, and we estimate relative emissions of N2O and CH4 from different alternative fuel passenger cars, light-duty trucks, and heavy-duty vehicles.  相似文献   

18.
In recent studies, proxy XCH4 retrievals from the Japanese Greenhouse gases Observing SATellite (GOSAT) have been used to constrain top-down estimation of CH4 emissions. Still, the resulting interannual variations often show significant discrepancies over some of the most important CH4 source regions, such as China and Tropical South America, by causes yet to be determined. This study compares monthly CH4 flux estimates from two parallel assimilations of GOSAT XCH4 retrievals from 2010 to 2019 based on the same Ensemble Kalman Filter (EnKF) framework but with the global chemistry transport model (GEOS-Chem v12.5) being run at two different spatial resolutions of 4° × 5° (R4, lon × lat) and 2° × 2.5° (R2, lon × lat) to investigate the effects of resolution-related model errors on the derived long-term global and regional CH4 emission trends. We found that the mean annual global methane emission for the 2010s is 573.04 Tg yr –1 for the inversion using the R4 model, which becomes about 4.4 Tg yr –1 less (568.63 Tg yr –1) when a finer R2 model is used, though both are well within the ensemble range of the 22 top-down results (2008–17) included in the current Global Carbon Project (from 550 Tg yr –1 to 594 Tg yr –1). Compared to the R2 model, the inversion based on the R4 tends to overestimate tropical emissions (by 13.3 Tg yr –1), which is accompanied by a general underestimation (by 8.9 Tg yr –1) in the extratropics. Such a dipole reflects differences in tropical–mid-latitude air exchange in relation to the model’s convective and advective schemes at different resolutions. The two inversions show a rather consistent long-term CH4 emission trend at the global scale and over most of the continents, suggesting that the observed rapid increase in atmospheric methane can largely be attributed to the emission growth from North Africa (1.79 Tg yr –2 for R4 and 1.29 Tg yr –2 for R2) and South America Temperate (1.08 Tg yr –2 for R4 and 1.21 Tg yr –2 for R2) during the first half of the 2010s, and from Eurasia Boreal (1.46 Tg yr –2 for R4 and 1.63 Tg yr –2 for R2) and Tropical South America (1.72 Tg yr–2 for R4 and 1.43 Tg yr –2 for R2) over 2015–19. In the meantime, emissions in Europe have shown a consistent decrease over the past decade. However, the growth rates by the two parallel inversions show significant discrepancies over Eurasia Temperate, South America Temperate, and South Africa, which are also the places where recent GOSAT inversions usually disagree with one other.  相似文献   

19.
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.  相似文献   

20.
Extensive ambient concentration and flux measurements have been performed in the heavily polluted region of Cubatão/Brazil. Substantial contribution of anthropogenic sources to the local reduced sulfur burden has been observed. As a result of this atmospheric sulfur burden average gas exchange between vegetated soils and the atmosphere shows net deposition. Based mainly on own field measurements a local budget for H2S, COS, and CS2 has been made up in order to calculate anthropogenic emissions. All major sources and sinks in the chosen atmospheric reservoir (24×20×1 km) have been taken into account. Due to the small reservoir size fluxes across its boundaries are dominant sources and sinks. The differences between outflux and influx therefore account for the unknown anthropogenic emissions which have been determined to be 80±10 (H2S), 66±15 (COS), and 29±6 Mmol year-1 (CS2). Other sources and sinks like natural emissions, chemical conversion, and dry deposition turned out to be of minor importance on a local scale. In fact, inside the investigated reservoir natural emissions were below 0.5% of anthropogenic emissions. Anthropogenic emissions of H2S, COS, and CS2 quantified in this work have been compared with global emission estimates for these compounds made by other authors. We conclude that global anthropogenic emissions of reduced sulfur compounds especially of COS and CS2 are currently under-estimated.  相似文献   

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