内蒙古桌子山煤田火区特征及灭火方法探讨

内蒙古自治区桌子山煤田赋存着较为稀缺的煤种一焦煤,煤田内存在的火区不仪烧掉了宝贵的焦性煤炭资源,给煤矿生产带来严重的事故隐患,对当地生态环境也造成极大的破坏。经查明区内有26处子火区,分布面积约760万m^2,通过煤田地质特征、煤质特征、地表指示特征、同位素氡气的浓度相对分布特征、物性特征分析了区内煤层发火原因,根据桌子山煤田火区特点,建议采用浅剥、深灌与覆盖相结合的灭火方法,并对火区进行动态监测。     

Biomass burning in the tropical savannas of Ivory Coast: An overview of the field experiment Fire of Savannas (FOS/DECAFE 91)

FOS/DECAFE 91 (Fire of Savannas/Dynamique et Chimie Atmosphérique en Forêt Equatoriale) was the first multidisciplinary experiment organized in Africa to determine gas and aerosol emissions by prescribed savanna fires. The humid savanna of Lamto in Ivory Coast was chosen for its ecological characteristics representative of savannas with a high biomass density (900 g m^–2 dry matter). Moreover the vegetation and the climate of Lamto have been studied for more than twenty years. The emission ratios (X/CO₂) of the carbon compounds (CO₂, CO, NMHC, CH₄, PAH, organic acids and aerosols), nitrogen compounds (NO_x, N₂O, NH₃ and soluble aerosols) and sulfur compounds (SO₂, COS and aerosols) were experimentally determined by ground and aircraft measurements. To perform this experiment, 4 small plots (100×100 m) and 2 large areas (10×10 km) were prepared and burnt in January 1991 during the period of maximum occurrence of fires in this type of savanna. The detailed ecological study shows that the carbon content of the vegetation is constant within 1% (42 g C for 100 g of vegetal dry matter), the nitrogen content (0.29 g N for 100 g of dry matter) may vary by 10% and the sulfur content (0.05 g S/100 d.m.) by 20%. These variations of the biomass chemical content do not constitute an important factor in the variation of the gas and particle emission levels. With the emission ratios characteristic of humid savanna and flaming conditions (CO/CO₂ of 6.1% at the ground and 8% for airborne measurements), we propose a set of new emission factors, taking into account the burning efficiency which is about 80%: 74.4% of the carbon content of the savanna biomass is released to the atmosphere in the form of CO₂, 4.6% as CO, 0.2% as CH₄, 0.5% as NMHC and 0.7% as aerosols. 17.2% of the nitrogen content of the biomass is released as NO_x, 3.5% as N₂O, 0.6% as NH₃ and 0.5% as soluble aerosols.     

Particulate content of savanna fire emissions

As part of the FOS-DECAFE experiment at Lamto (Ivory Coast) in January 1991, various aerosol samples were collected at ground level near prescribed fires or under local background conditions, to characterize the emissions of particulate matter from the burning of savanna vegetation. This paper deals with total aerosol (TPM) and carbon measurements. Detailed trace element and polycyclic hydrocarbon data are discussed in other papers presented in this issue.Near the fire plumes, the aerosols from biomass burning are primarily of a carbonaceous nature (C%70% of the aerosol mass) and consist predominantly of submicron particles (more than 90% in mass.) They are characterized by their organic nature (black to total carbon ratio Cb/Ct in the range 3–20%) and their high potassium content (K/Cb0.6). These aerosols undergo aging during their first minutes in the atmosphere causing slight alterations in their size distribution and chemical composition. However, they remain enriched in potassium (K/Cb=0.21) and pyrene, a polycyclic aromatic hydrocarbon, such that both of these species may be used as tracers of savanna burning aerosols. We show that during this period of the year, the background atmosphere experiences severe pollution from both terrigenous sources and regional biomass burning (44% of the aerosol). Daynight variations of the background carbon concentrations suggest that fire ignition and spreading occur primarily during the day. Simultaneous TPM and CO₂ real-time measurements point to a temporal and spatial heterogeneity of the burning so that the ratio of the above background concentrations (TPM/CO₂) varies from 2 to 400 g/kg C. Smoldering processes are intense sources of particles but particulate emissions may also be important during the rapidly spreading heading fires in connection with the generation of heavy brown smoke. We propose emission factor values (EF) for aerosols from the savanna biomass burning aerosols: EF (TPM)=11.4±4.6 and 69±25 g/kg C_{dry plant} and EF(Ct)=7.4±3.4 and 56±16 g C/kg C_{dry plant} for flaming and smoldering processes respectively. In these estimates, the range of uncertainty is mostly due to the intra-fire variability. These values are significantly lower than those reported in the literature for the combustion of other types of vegetation. But due to the large amounts of vegetation biomass being burnt in African savannas, the annual flux of particulate carbon into the atmosphere is estimated to be of the order of 8 Tg C, which rivals particulate carbon emissions from anthropogenic activities in temperate regions.     

卫星遥感在秸秆焚烧监测中的应用

通过对MODIS光谱特征的分析，提出了一种综合运用3S技术进行秸秆焚烧动态监测的资料处理流程和量化判识指标。通过在关中地区2004年麦秸秆焚烧监测中的应用，效果良好，为政府部门迅速、准确地了解全省秸秆焚烧情况，提高预警能力和监督检查的效率提供了科学依据。     

Satellite-measured atmospheric aerosol content in Korea: anthropogenic signals from decadal records

Spatiotemporal characteristics and anthropogenic signals of aerosol optical thickness (AOT) distributions over Korea are investigated in this study using AOT time-series data from the Moderate Resolution Imaging Spectroradiometer (MODIS). AOT observations, a quantitative measure of the atmospheric quality, had significant geographical variations during the study period (2000–2010). Comparing metro cities or counties with similar populations, western regions showed higher AOT values than eastern regions. Particular matter with a diameter < 10 µm (PM₁₀), including aeolian dust or yellow dust, is the primary component of atmospheric aerosols, and their transport into the region has shown a strong seasonal pattern with its peak from March to April and lows from July to September. These seasonal dust patterns, however, did not correspond well to temporal AOT records, which typically reached the maximum level in June nationwide. Rather, widespread regional fire events and humidity showed significant correlations with AOT time-series. This correlation rapidly increased as the range of fire occurrence was extended to the west as far as 115°E. The relative humidity also had a significant correlation with AOT during the month of June. In addition to urban emission of anthropogenic aerosols, regional biomass burning and secondary growth of hygroscopic aerosols are considered important contributors to the degradation of the atmospheric environment during the non-Asian Dust season over the Korean Peninsula.     

2015年11月沈阳地区一次PM2.5重污染过程综合分析

利用多源观测资料综合分析了2015年11月沈阳地区一次PM2.5 重污染天气的气象条件、垂直风场演变、大气边界层特征以及污染物的来源。结果表明:本次重污染过程中,沈阳市区PM2.5浓度长达81h超过250μg · m^-3 ,其中峰值浓度达到1287μg · m^-3 ,重污染期间PM2.5 /PM10 的比例最高为90%。受地面倒槽和黄淮气旋影响,近地面层持续存在的逆温层、高相对湿度和弱偏北风为颗粒物吸湿增长和长时间聚集提供有利的天气条件。风廓线雷达风场资料显示在重污染期间,近地面层存在弱风速区、凌乱风场和弱下沉气流。利用风廓线雷达资料计算了边界层通风量(Ventilation Index,VI)和局地环流指数(Recirculation,R),边界层通风量VI和PM2.5 存在明显的负相关,非污染日VI是重污染日的2倍,局地环流指数R在重污染天气前大于0.9,而在污染期间部分空间R小于0.8。通过后向轨迹模式和火点监测资料分析发现,沈阳上空300m高度气团来自于生物质燃烧区域,而且沈阳地区NO2和CO浓度的变化与PM2.5一致,说明本次重污染过程也可能和生物质燃烧有关。     

淮河流域秸秆焚烧关键期主要大气污染物浓度时空分布特征

基于2015年6月淮河流域卫星遥感监测火点信息、环境空气质量监测数据和常规气象观测资料,利用ANUSPLIN和ArcGISKriging方法对气象要素和主要大气污染物浓度空间栅格化,分析了秸秆焚烧关键期内AQI和主要污染物浓度的时空变化特征及其与气温、相对湿度、风速等气象要素的相关关系。结果表明:秸秆焚烧关键期内,淮河流域城市AQI、PM10与PM2.5浓度均明显升高,且与卫星监测火点具有一定时空响应关系。在时间变化上,AQI、PM10与PM2.5浓度6月上中旬呈波动上升,6月下旬趋于回落;在空间分布方面,AQI、PM10与PM2.5浓度三者分布形态相似,总体上呈现"南低北高、两高一低"分布特征;期间AQI、PM10与PM2.5浓度与气温呈显著正相关,与相对湿度呈显著负相关,与风速的相关性不显著。     

京津冀周边秸秆燃烧对PM2.5无机组分影响

华北平原是我国主要农作物产区,田间秸秆焚烧现象普遍存在,选取秋收季节（2014年10月）分析了秸秆燃烧的排放特征,利用区域化学传输模型WRF-Chem模拟研究了燃烧排放对气态前体物及其氧化产物的影响,以及最终导致的PM_2.5中硫酸盐、硝酸盐和铵盐的变化。研究表明:2014年秋收季节,河南和山东等省份的秸秆燃烧排放会在东南风的输送作用下影响京津冀地区;秸秆燃烧排放大量挥发性有机物（VOCs）,导致火点源及周边地区大气中主要氧化剂浓度上升,提升了区域大气氧化能力;当携带大量VOCs的秸秆燃烧烟羽与以化石燃料排放为主的城市气团相混合时,大气氧化性增强会加速城市地区人为源排放的NO_x和SO₂等气态前体物的氧化过程,提高硫酸盐和硝酸盐的形成速率、促进二次无机气溶胶的生成。     

Re‐establishment of soil water repellency after destruction by intense burning in a Mediterranean heathland (SW Spain)

Soil water repellency has been conventionally considered as a fire‐induced effect, but an increasing number of studies have suggested that natural background repellency occurs in many soil types, and many of them have suggested that water repellency can be re‐established over time after being destroyed. An experimental fire was conducted to study changes of the soil surface during the first 18 months following intense burning. The main objectives of this paper are as follows: (1) to investigate in situ water repellency changes at three soil depths (0, 2 and 4 cm) immediately after burning; (2) to evaluate the medium‐term evolution of water repellency under field conditions; and (3) to outline the main hydrological consequences of these changes. Also, different water repellency tests (water drop penetration time, ethanol percentage test (EPT) and contact angle (CA) between water drops and the soil surface) were carried out for comparison purposes. Field experiments showed that soil water repellency was partly destroyed after intense burning. Changes were relatively strong at the soil surface, but diminished progressively with depth. Levels of water repellency were practically re‐established 18 months after burning. This suggests that water repellency in the studied area is not necessarily a consequence of fire, but can instead be a natural attribute. Finally, although limited in time, destruction of soil water repellency has important consequences for runoff flow generation and soil loss rates, and, indirectly, for water quality. Copyright © 2009 John Wiley & Sons, Ltd.     

Isoprene emissions from vegetation and hydrocarbon emissions from bushfires in tropical Australia

Information from a variety of sources, including an airborne field expedition in November 1985, is used to produce estimates of the annual emissions of some hydrocarbons from bushfires, and isoprene from trees, in tropical Australia. For the continent north of 23° S the annual bushfires (biomass burning) input was estimated, in units of Tg carbon, to be 2 TgC (uncertainty range 0.8–5 TgC), emitted predominantly during the May to October dryseason. Isoprene emissions during this period were estimated also to be 2 TgC (uncertainty range 0.5–8 TgC), but were estimated to be an order of magnitude higher during the November to April wet season, at a level of 23 TgC (uncertainty range 6–100 TgC).The large annual emission of isoprene over the tropical part of the Australian continent yields ppbv levels of isoprene measured at the surface in summertime. Isoprene reactivity with hydroxyl radical is such that at these concentrations isoprene must be a dominant factor in controlling the concentration of OH radical in the convective boundary layer. Simple arguments based on the convective velocity scale suggest that the shape of the isoprene vertical profile in November 1985 would be consistent with available data on the OH-isoprene reaction rate if OH concentration in the boundary layer averaged about 2.5×10⁶ cm^-3 over the middle part of the day.Temporarily at the International Meteorological Institute, Stockholm University, S-106 91, Stockholm, Sweden.