首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到20条相似文献，搜索用时 15 毫秒
1.
Emission rates of biogenic volatile organic compounds emitted by the forests were estimated for five geographical regions as well as for all Switzerland. Monoterpene and isoprene emissions rates were calculated for each main tree species separately using the relevant parameters such as temperature, light intensity and leaf biomass density. Biogenic emissions from the forests were found to be about 23% of the total annual VOC emissions (anthropogenic and biogenic) in Switzerland. The highest emissions are in July and lowest in January. Calculations showed that the coniferous trees are the main sources of the biogenic emissions. The major contribution comes from the Norway spruce (picea abies) forests due to their abundance and high leaf biomass density. Although broad-leaved forests cover 27% of all the forests in Switzerland, their contribution to the biogenic emissions is only 3%. Monoterpenes are the main species emitted, whereas only 3% is released as isoprene. The highest emission rates of biogenic VOC are estimated to be in the region of the Alps which has the largest forest coverage in Switzerland and the major part of these forests consists of Norway spruce. The total annual biogenic VOC emission rate of 87 ktonnes y–1 coming from the forests is significantly higher than those from other studies where calculations were carried out by classifying the forests as deciduous and coniferous. The difference is attributed to the high leaf biomass densities of Norway spruce and fir (abies alba) trees which have a strong effect on the results when speciation of trees is taken into account. Besides the annual rate, emission rates were calculated for a specific period during July 4–6, 1991 when a photochemical smog episode was investigated in the Swiss field experiment POLLUMET. Emission rates estimated for that period agree well with those calculated for July using the average temperatures over the last 10 years.  相似文献   

2.
A set of daily PM10 (n = 281) samples collected from April 2001 to April 2002 at a rural site (Erdemli), located on the coast of the Eastern Mediterranean, were analyzed applying Mass Closure (MC), absolute principal factor analysis (APFA) and Positive Matrix Factorization (PMF) to determine source contributions. The results from the three techniques were compared to identify the similarities and differences in the sources and source contributions. Source apportionment analysis indicated that PM10 were mainly originated from natural sources (sea salt + crustal ≈ 60%) whilst secondary aerosols and residual oil burning accounted for approximately 20% and 10% of the total PM10 mass, respectively. Calculations for sulfate showed that on average 8% and 12% of its total concentration were originated from sea salt and biogenic emissions, respectively. However, the contribution by biogenic emissions may reach up to a maximum of ~ 40% in the summer. Potential Source Contribution Function (PSCF) analysis for identification of source regions showed that the Saharan desert was the main source area for crustal components. For secondary aerosol components the analysis revealed one source region, (i.e. the south-Eastern Black Sea), whereas for residual oil, Western Europe and the western Balkans areas were found to be the main source regions.  相似文献   

3.
Presented is a detailed comparison of CH4 and δ13C–CH4 measurements with simulations of the global transport model TM3. Experimental data were obtained during campaigns along the Trans-Siberian railroad in the framework of the TROICA project. Two summer (1999 and 2001) and one spring (2003) expeditions are evaluated. Model simulations include sensitivity tests to further investigate the isotopic composition of natural gas and emissions from Siberian wetlands. Comparison of the average mixing ratio of methane and its isotopic composition (δ13C) has been performed for different geographic zones, including the European part of Russia, Western Siberia and Central Siberia. Simulations are in reasonable agreement with the measurements for the European part of Russia and confirm a high contribution of natural gas to the observed methane levels. An increase of emission from bogs shifts the simulated methane isotopic composition closer to the observations. The relative importance of the Western Siberia emissions in current inventories is underestimated in comparison with other wetland regions in the former USSR. Simulated average mixing ratios are in a good agreement with the observations in Central Siberia, while 13C(CH4) values tend to be higher than measured in all considered scenarios. These results point to a bias in the modeled source mixture over Russia, which could be repaired by shifting emissions from isotopically heavy methane sources (e.g. coal, oil or biomass burning) to light sources (e.g. wetlands, ruminants, waste treatment). Alternatively, the average isotopic signature of Siberian wetlands may be lighter than expected.  相似文献   

4.
本文利用气体组分及大气气溶胶在线监测系统(MARGA ADI 2080)观测武汉市2018年1月9—26日大气气溶胶中的8种水溶性离子(NH+4、NO-3、SO2-4、Cl-、K+、Ca2+、Na+和Mg2+),结合气象要素数据,使用主成分分析(PCA)、正定矩阵因子分析法(PMF)、HYSPLIT后向轨迹模式、潜在源区贡献(PSCF)和浓度权重轨迹(CWT),对霾污染过程中水溶性离子进行了全面的来源解析,探究了霾不同阶段下来源差异和空间分布特征。结果表明:(1)本次霾污染中的8种水溶性离子和4种污染气体,PCA解析出的源和占比分别为二次源和燃煤源的混合源(41.28%)、工业排放和土壤扬尘混合源(27.73%)和机动车排放源(9.63%),PMF解析出的源和占比分别为燃煤与土壤扬尘混合源(18.57%)、机动车排放源(20.74%)、二次源(18.30%)、光化学污染源(22.24%)和燃煤源(20.15%)。(2)霾在不同阶段下水溶性离子和4种污染气体的来源存在差异,在清洁天和霾消散阶段,光化学的贡献最高,占比分别为31.42%和36.07%;在霾发生阶段燃煤与土壤扬尘源的贡献最高,其贡献为40.94%;在霾发展阶段,最大的控制源为二次源,贡献占比为37.51%。(3)此次武汉市霾污染中PM2.5浓度和NH+4、NO-3和SO2-4的潜在源区为皖豫鄂三省和赣湘鄂三省交界处。霾污染中PM2.5的主要影响范围是武汉市南部和北部省份,NO-3、NH+4和SO2-4的主要影响区域为武汉市东北方向的城市、湖南省和江西省。  相似文献   

5.
The impacts of emissions from industry,power plant,transportation,residential,and biogenic sources on daily maximum surface ozone （O3DM） over the Beijing-Tianjin-Hebei （BTH） region in North China in the summer of 2007 were examined in a modeling study.The modeling system consisted of the Weather Research and Forecasting （WRF） model and the photochemical dispersion model,CAMx.The factor separation technique （FST） was used to quantify the effect of individual emission source types and the synergistic interactions among two or more types.Additionally,the effectiveness of emission reduction scenarios was explored.The industry,power plant,and transportation emission source types were found to be the most important in terms of their individual effects on O3DM.The key contributor to high surface O3 was power plant emissions,with a peak individual effect of 40 ppbv in the southwestern BTH area.The individual effect from the biogenic emission category was quite low.The synergistic effects from the combinations of each pair of anthropogenic emission types suppressed O3 formation,while the synergistic effects for combinations of three were favorable for O3 formation when the industrial and power plant emission source types coexisted.The quadruple synergistic effects were positive only with the combination of power plant,transportation,residential,and biogenic sources,while the quintuple synergistic effect showed only minor impacts on O3DM concentrations.A 30％ reduction in industrial and transportation sources produced the most effective impacts on O3 concentrations,with a maximum decrease of 20 ppbv.These results suggested that the synergistic impacts among emission source types should be considered when formulating emission control strategies for O3 reduction.  相似文献   

6.
Concentrations of thirty-five trace elements in ambient fine particulate matter (PM2.5) were measured from September 2001 to January 2002 in Mira Loma, a semi-urban area in southern California. The most abundant species were found to be sulfur (S; 23% of the total trace element concentration), followed by Si, Fe, Ca, and Al (soil-related elements; 51% of the total). In general, total trace element concentrations were found to be significantly higher for the drier months of September and October, compared to December and January. Factor analysis, enrichment factor (EF) analysis, and ratio analysis (Al/Zn) revealed a significant contribution of soil-related sources to the ambient trace elements for PM2.5 in the study area. Other important contributors to the trace elements in ambient PM2.5 in Mira Loma included motor vehicle-related emissions (brake pads, lubricant oils, gasoline, and diesel combustion), secondary sulfates, sea salts, and biomass burning. The influence of sea salts on the study area was identified using a backward trajectory analysis.  相似文献   

7.
以武汉市为研究区域,基于实地调查获得典型行业污染源活动水平,以大气污染物排放清单编制技术指南为参考,利用排放因子法建立2014年武汉市大气污染源排放清单,并结合经纬度、人口密度分布、土地利用类型、道路长度等数据将排放清单进行了3 km×3 km网格化处理.结果表明,2014年武汉市SO2、NOx、PM10、PM2.5、CO、BC、OC、VOCs和NH3排放量分别为10.3、17.0、16.3、7.1、63.1、0.6、0.4、19.8和1.6万t.固定燃烧源为SO2排放的主要来源,其贡献率约64%;移动源为NOx的主要来源,其贡献率约51%;颗粒物排放主要来源于扬尘源和工艺过程源;CO和VOCs主要来源于工艺过程源,BC和OC排放均以移动源和生物质燃烧源为主,NH3排放主要来自农业源.污染物排放主要集中在青山区至新洲区一带.  相似文献   

8.
中国大陆黑碳气溶胶排放清单   总被引：1，自引：0，他引：1  
The detailed high-resolution emission inventory of black carbon (BC) from China in the year 2000 was calculated. The latest fuel consumption data including fossil and biomass fuels, and socio-economic statistics used were obtained from government agencies, mostly at the county level, and some new emission factors (Efs) from local measurements were also used. National and regional summaries of emissions were presented at 0.2°×0.2°resolution. Total BC emission was 1499.4 Gg in 2000, mainly due to the burning of coal and biomass. The BC emission estimated here is higher than those in previous studies, mainly because the emissions from coal burning by rural industries and residences were previously underestimated. More BC aerosols were emitted from eastern China than western China. A strong seasonal dependence was observed for BC emissions, with peaks in January and December and low emissions in July and August; and this seasonality is mainly due to patterns in residential heating and the open burning of crop residues.  相似文献   

9.
Ammonia emissions from stored farm manures form a small but significant proportion (∼10%) of the total emitted annually from UK sources. These emissions are regulated by factors including: the surface area of the store; the storage method; the physical form of the stored manure and the source of manure. A method was developed to estimate in situ emissions from a range of store types (weeping wall and earth-banked lagoon) that are currently under-represented in UK emissions estimates. Passive diffusion samplers (Willems Badges) were used to determine vertical concentration profiles to a height of 4.5 m at a number of locations around each slurry store. An atmospheric dispersion model was applied to estimate the contribution from emissions from other on-farm ammonia sources to the measured data and also to determine the emission rates from the stored manure. A procedure was applied whereby the emission rates from each source were allowed to vary and a numerical equation solver was applied to backfit the modelled data set to the field measurements. Measurements were collected at four farms on a monthly basis throughout the year, with each dataset being collected over 24 h. The uncertainties in the estimates of emissions from the slurry stores during individual measurement periods typically ranged between 20–40% though higher uncertainties occurred when emission fluxes from the stores were below 0.25 g NH3–N m−2 day−1 and were entrained in the wakes, and mixed with the emissions, of adjacent buildings. The average emission from the farms was 0.6 g NH3–N m−2 day−1 which agrees with other recent data on ammonia emissions from crusted slurry stores and, though it is within the range of data considered in the UK emissions inventory, suggests that emissions from weeping wall stores and earth-banked lagoons may be currently overestimated in national predictions.  相似文献   

10.
The purpose of this paper is to describe global urban greenhouse gas emissions by region and sector, examine the distribution of emissions through the urban-to-rural gradient, and identify covariates of emission levels for our baseline year, 2000. We use multiple existing spatial databases to identify urban extent, greenhouse gas emissions (CO2, N2O, CH4 and SF6) and covariates of emissions in a “top-down” analysis. The results indicate that urban activities are significant sources of total greenhouse gas emissions (36.8 and 48.6 % of total). The urban energy sector accounts for between 41.5 and 66.3 % of total energy emissions. Significant differences exist in the urban share of greenhouse gas emissions between developed and developing countries as well as among source sectors for geographic regions. The 50 largest urban emitting areas account for 38.8 % of all urban greenhouse gas emissions. We find that greenhouse gas emissions are significantly associated with population size, density, growth rates, and per capita income. Finally, comparison of our results to “bottom-up” estimates suggest that this research’s data and techniques are best used at the regional and global scales.  相似文献   

11.
We traced the adjoint sensitivity of a severe pollution event in December 2016 in Beijing using the adjoint model of the GRAPES–CUACE (Global/Regional Assimilation and Prediction System coupled with the China Meteorological Administration Unified Atmospheric Chemistry Environmental Forecasting System). The key emission sources and periods affecting this severe pollution event are analyzed. For comaprison, we define 2000 Beijing Time 3 December 2016 as the objective time when PM2.5 reached the maximum concentration in Beijing. It is found that the local hourly sensitivity coefficient amounts to a peak of 9.31 μg m–3 just 1 h before the objective time, suggesting that PM2.5 concentration responds rapidly to local emissions. The accumulated sensitivity coefficient in Beijing is large during the 20-h period prior to the objective time, showing that local emissions are the most important in this period. The accumulated contribution rates of emissions from Beijing, Tianjin, Hebei, and Shanxi are 34.2%, 3.0%, 49.4%, and 13.4%, respectively, in the 72-h period before the objective time. The evolution of hourly sensitivity coefficient shows that the main contribution from the Tianjin source occurs 1–26 h before the objective time and its peak hourly contribution is 0.59 μg m–3 at 4 h before the objective time. The main contributions of the Hebei and Shanxi emission sources occur 1–54 and 14–53 h, respectively, before the objective time and their hourly sensitivity coefficients both show periodic fluctuations. The Hebei source shows three sensitivity coefficient peaks of 3.45, 4.27, and 0.71 μg m–3 at 4, 16, and 38 h before the objective time, respectively. The sensitivity coefficient of the Shanxi source peaks twice, with values of 1.41 and 0.64 μg m–3 at 24 and 45 h before the objective time, respectively. Overall, the adjoint model is effective in tracking the crucial sources and key periods of emissions for the severe pollution event.  相似文献   

12.
We measured the emissions of volatile aliphatic amines and ammonia produced by the manure of beef cattle, dairy cows, swine, laying hens and horses in livestock buildings. The amine emissions consisted almost exclusively of the three methylamines and correlated with those of ammonia. The molar emission ratios of the methylamines to ammonia, and data on NH3 emissions from animal husbandry in Europe, together with global statistics on domestic animals, were used to estimate the global emissions of amines. Annual global methylamine-N input to the atmosphere from animal husbandry in 1988 was 0.15±0.06 TgN (Tg=1012 g). Almost 3/4 of these emissions consisted of trimethylamine-N. This represents about half of all methylamine emissions to the atmosphere. Other sources are marine coastal waters and biomass burning.Possible reaction pathways for atmospheric methylamines are shown. Among various speculative but possible products N2O and HCN are of interest because the emission of methylamines could contribute to the global budgets of these compounds. Maximum atmospheric N2O production from methylamines are below 0.4 Tg N/year, which is less than 10% of the annual N2O growth rate. Although we do not expect the methylamine emissions to contribute in a major way to the atmospheric N2O budget, more studies are needed to establish this conclusion beyond doubt. Similar conclusions hold for HCN.  相似文献   

13.
The allocation of CO2 emissions to specific sources is a major policy issue for international aviation, especially for determining allocations for emissions trading schemes. This paper addresses the problem by recommending a possible methodology to allocate emissions to specific sources using detailed air traffic data. The basis for the calculations is an air traffic sample for one full-day of traffic from the UK. In order to analyse aircraft fuel burn use and hence CO2 emissions, the Reorganized Air Traffic Control Mathematical Simulator (RAMS Plus) and the Advanced Emission Model (AEM III) are used. The results from these detailed simulations are compared with two of the most widely-used aviation CO2 emission estimates to have been made for the UK: the SERAS study and NETCEN estimate. Their estimates for the year 2000 are 26.1 and 31.4 Mt, respectively. In addition, the most recent NETCEN estimate for the year 2003 is 34.1 Mt of CO2. Our estimate of total aviation CO2 emissions, using detailed simulations and real air traffic data, is 34.7 Mt for the year 2004. In addition, emission estimates are compared with two global aviation emission inventories: AERO2K and SAGE. Contributions of the highest-emitting flights and aircraft types are identified. International departures dominate; 6% of flights account for 50% of total emissions. The largest aircraft emit the most per flight-km, although not per passenger-km. Different methodologies and their implications are also discussed.  相似文献   

14.
于2016年7月-2017年6月在武汉市典型居民区对大气中101种挥发性有机物（VOCs）进行了监测,以便研究武汉市典型居民区周边VOCs的组成特征和变化规律,并探讨了其主要来源.结果表明,武汉市空气中VOCs的体积分数为（46.24±24.57）×10-9,表现为烷烃>含氧有机物>烯烃>卤代烃>芳香烃.受交通排放影响烷烃的比例上午高于下午,1月机动车尾气为武汉市主要的VOCs排放源,夏季含氧类化合物浓度高于冬季,可能更多地受本地喷涂等溶剂使用行业和光化学反应生成的影响,5-9月表现出明显的生物源排放特征.利用正交矩阵因子分析（PMF）得到武汉市居民区大气VOCs主要有6个来源,分别为燃烧源、机动车尾气、工业排放、溶剂使用、汽油挥发和植物排放.其中,燃烧源、机动车尾气贡献比例最高,是该区域VOCs控制的重要排放源.  相似文献   

15.
大气污染物排放清单是空气质量模拟和空气污染治理的重要依据.本研究比较分析了两套覆盖江苏省的2017年大气污染物排放清单，即分别由上海市环境科学研究院、江苏省环境科学研究院编制的"长三角清单"和"江苏省清单"，并结合区域空气质量模型CMAQ评估不同清单对长三角地区2017年1、4、7、10月的空气质量模拟的影响.清单比较结果表明，除二氧化硫（SO2）以外，江苏省清单估算的各污染物排放量较长三角清单低.通过与观测数据比较，发现两套清单对SO2、氮氧化物（NOx）、臭氧（O3）和细颗粒物（PM2.5）的模型模拟性能均较好.江苏省清单与长三角清单两者的模拟结果空间分布接近，其中江苏省清单模拟的PM2.5和O3在长三角多数地区略低于长三角清单的模拟结果（1月O3除外）.江苏省清单与长三角清单均能够用于空气质量模式模拟，可为江苏地区的细颗粒物和光化学烟雾污染的控制策略制定提供参考.  相似文献   

16.
An improvement of methods for the inventory of greenhouse gas (GHG) emissions is necessary to ensure effective control of commitments to emission reduction. The national inventory reports play an important role, but do not reflect specifics of regional processes of GHG emission and absorption for large-area countries. In this article, a GIS approach for the spatial inventory of GHG emissions in the energy sector, based on IPCC guidelines, official statistics on fuel consumption, and digital maps of the region under investigation, is presented. We include mathematical background for the spatial emission inventory of point, line and area sources, caused by fossil-fuel use for power and heat production, the residential sector, industrial and agricultural sectors, and transport. Methods for the spatial estimation of emissions from stationary and mobile sources, taking into account the specifics of fuel used and technological processes, are described. Using the developed GIS technology, the territorial distribution of GHG emissions, at the level of elementary grid cells 2 km?×?2 km for the territory of Western Ukraine, is obtained. Results of the spatial analysis are presented in the form of a geo-referenced database of emissions, and visualized as layers of digital maps. Uncertainty of inventory results is calculated using the Monte Carlo approach, and the sensitivity analysis results are described. The results achieved demonstrated that the relative uncertainties of emission estimates, for CO2 and for total emissions (in CO2 equivalent), depend largely on uncertainty in the statistical data and on uncertainty in fuels’ calorific values. The uncertainty of total emissions stays almost constant with the change of uncertainty of N2O emission coefficients, and correlates strongly with an improvement in knowledge about CH4 emission processes. The presented approach provides an opportunity to create a spatial cadastre of emissions, and to use this additional knowledge for the analysis and reduction of uncertainty. It enables us to identify territories with the highest emissions, and estimate an influence of uncertainty of the large emission sources on the uncertainty of total emissions. Ascribing emissions to the places where they actually occur helps to improve the inventory process and to reduce the overall uncertainty.  相似文献   

17.
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   

18.
Soil dust aerosol is the largest contributor to aerosol mass concentrations in the troposphere and has considerable effects on air quality and climate. Arid and semi-arid areas of East Asia are one of the important dust source regions thus it is crucial to understand dust mobilization and accurately estimate dust emissions in East Asia. However, present dust models still contain large uncertainties with dust emissions that remain a significant contributor to the overall uncertainties in the model. In this study, we attempt to reduce these uncertainties by using an inverse modeling technique and obtain optimized dust emissions. We use Moderate Resolution Imaging Spectrometer (MODIS) aerosol optical depths (AODs) and groundbased mass concentrations of particles less than 10 μm in aerodynamic diameter (PM10) observations over East Asia in May 2007. The MODIS AODs are validated with AErosol RObotic NETwork (AERONET) AODs. The inversion uses the maximum a posteriori method and the GEOS-Chem chemical transport model (CTM) as a forward model. The model error is large over dust source regions including the Gobi Desert and Mongolia. We find that inverse modeling analyses from the MODIS and PM10 observations consistently result in decrease of dust emissions over Mongolia and the Gobi Desert. Whereas over the Taklamakan Desert and Manchuria, the inverse modeling analyses from both observations yield contrast results such as increase of dust sources using MODIS AODs, while decrease of those using PM10 observations. We discuss some limitations of both observations to obtain the optimized dust emissions and suggest several strategies for the improvement of dust emission estimates in the model.  相似文献   

19.
基于排放因子法建立了2006-2017年安徽省人为源氨排放清单,估算人为源氨的排放水平、变化趋势及其分布特征。结果表明,安徽省2017年人为源氨排放量较高的两个地区是阜阳市和六安市,而氨排放总量最小的是马鞍山,占全省氨排放总量的1.83%。安徽省氨平均排放强度为5.34 t·km-2,其中阜阳市、淮南市及蚌埠市的排放强度均超过7 t·km-2。2006-2017年畜禽养殖源产生的氨排放量处于增加状态,尤其是肉猪、肉鸡和肉鸭的贡献分别占到畜禽源氨排放总量的34.49%~38.39%、20.31%~32.8%和10.40%~16.42%。而氮肥施用导致的氨排放量表现出先增加后下降的趋势,2017年产生的氨排放量比2013年下降了28.71 kt。生物质燃烧、人体排放和氮肥生产是非农业源氨排放的主要来源,但由机动车产生的氨的贡献呈明显增长趋势,如从2006年的1.86%增长到2017年的7.47%,这与近年来安徽省汽车保有量不断增加有关。  相似文献   

20.
Results of research and practical experience confirm that stabilization of GHG concentrations will require a tremendous effort. One of the sectors identified as a significant source of methane (CH4) emissions are solid waste disposal sites (SWDS). Landfills are the key source of CH4 emissions in the emissions inventory of Slovakia, and the actual emission factors are estimated with a high uncertainty level. The calculation of emission uncertainty of the landfills using the more sophisticated Tier 2 Monte Carlo method is evaluated in this article. The software package that works with the probabilistic distributions and their combination was developed with this purpose in mind. The results, sensitivity analysis, and computational methodology of the CH4 emissions from SWDS are presented in this paper.  相似文献   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号