全球增暖的另一可能原因初探   总被引：14，自引：1，他引：14       下载免费PDF全文

李崇银  翁衡毅  高晓清  钟敏 《大气科学》2003,27(5):789-797

太阳是地球流体(大气和海洋等)运动的最终能量源,地球环境,尤其是气候的变化不能不与太阳活动有关.目前,普遍将全球增暖归结为温室气体含量增加所导致的温室效应的加剧,这无疑是有一定依据和有道理的.但从科学上来讲,人类活动所引起温室气体增加的影响,并非是唯一原因.基于已有的一些研究结果,从太阳活动的观点所进行的初步分析表明,太阳活动也可能是引起近世纪全球增暖的另一个重要原因.太阳活动的影响主要包括太阳辐射的直接影响和引发地磁场变化的间接影响两个方面,地球磁场的变化将可通过动力过程和热力过程而影响大气环流和气候的变化.  相似文献   

Resources of the ionized atmosphere as an aerosol source     

V.V. Smirnov  A.V. Savchenko 《Atmospheric Research》2006,82(3-4):554

The potential resources on the ion-stimulated syntheses effects of aerosol particles of lower troposphere in test sites in the arctic, mountain, arid and forest areas as the function of irradiation time and gas-precursor concentration were experimentally and theoretically evaluated. The dust-free outdoor air was irradiated with an ionization current of 10^− 6 A by α-rays from isotope ²³⁹Pu. The total output of radiolytic aerosols (RA) with a diameter of 3–1000 nm was found to be 0.05–0.1 molecules per 1 eV of absorbed radiation, while the physical upper limit is 0.25–0.4 molecules/eV. In an interval of exposition time from 6 to 800 s (adsorbed energy is 3 · 10¹²–10¹⁴ eV/cm³) the RA mass concentration at different sites was increased from 1–10 to 50–500 μg/m³. According to the liquid chromatography data the major RA material is the H₂O/HNO₃ solution with acid concentration  25%. The used physical model presents new aerosols as a product from small and intermediate ion association through formation of neutral clusters and describes adequately some of the peculiarities in field experiment data. Introducing SO₂, NH₃, and also hydrochloric, nitric and sulphuric acid vapours with concentration 0.1–1 mg/m³ in the irradiated air stimulated an increase of mass aerosol concentration by a factor of 8–30. The mean size also decreased by a factor of 3–5. These facts allowed us to expect that the chemical composition of radiolytic aerosols generated in outdoor air would noticeably differ after addition of the gas-precursors.  相似文献   

温室效应对青藏高原及青藏铁路沿线气候影响的数值模拟   总被引：25，自引：12，他引：13  

高学杰  李栋梁  赵宗慈  Filippo Giorgi 《高原气象》2003,22(5):458-463

在一个全球模式中嵌套了RegCM2区域气候模式,进行了CO2加倍对中国区域气候影响的数值试验,对青藏高原及青藏铁路沿线地区进行了重点分析。结果表明,在CO2加倍的情况下,这里的气温将明显升高,升高值一般在2．6～2．8℃以上,高于全国平均值。同时降水在青藏高原大部分地区也将明显增加;其中青藏铁路沿线的增加率一般在25％以上,远高于全国平均值水平。温室效应同时会使得青藏铁路沿线的日平均最高气温升高。  相似文献   

Sorption of carbon dioxide–methane mixtures     

Grayna Ceglarska-Stefa&#x;ska  Katarzyna Zar&#x;bska 《International Journal of Coal Geology》2005,62(4):211-222

The paper reports the results of experiments concerning the sorption/desorption processes, observed under laboratory conditions, in two types of coal extracted from operational coal-mines in Poland, using CH₄ and CO₂ to observe their relative inter-reaction with the coal samples when introduced in varying proportions and conditions. Numerous studies concerning the sorption/desorption phenomena have described the operational mechanisms and the relationship of mine gases to the organically-created coal-body in mines. The differences in the behaviour of certain gases is twofold: firstly the essentially different characteristics of CO₂ and CH₄, and secondly the structure of the coal-bed itself: its degree of metamorphism and content of macerals. From the results yielded, it was observed that the divergence of the isotherms of sorption of CH₄ and other gases in comparison with the isotherms of sorption of CO₂ and a CO₂/CH₄ mixture differed and that the curve on the sorption isotherm was more clearly distinct after the introduction of CO₂ molecules to the system: coal with a higher degree of metamorphism—CH₄, which is closely related to the rigidity of the structure according to the level of metamorphism. Since coals with higher carbon content exhibit lower molecular bonding than low-carbonised coals, the characteristic feature of the bonds in the first case is their mobility. Knowledge of the physical and chemical properties of hard coals, as well as their interaction with mining gases, is of great use in solving problems concerned with the extraction of methane from mines or its storage in goafs.  相似文献   

川西坳陷南段天然气来源与碳同位素地球化学研究   总被引：6，自引：0，他引：6       下载免费PDF全文

樊然学  周洪忠  蔡开平 《地球学报》2005,26(2):157-162

川西坳陷南段是四川盆地主要的天然气产区之一。前人对该区天然气的来源有多种见解。为了更清楚地认识此地区天然气的来源与运移，本文分析了平落坝、大兴西和白马庙气田16件天然气样品的C1-C4烃及CO2组份的碳同位素组成。所获得的同位素数据结合化学成份和地质资料表明，3个气田的烃类完全是热解成因的，都来源于气田下面的上三叠统烃源岩。这些气田的甲、乙烷碳同位素组成随深度呈不同规律的变化，这些变化归因于烃源岩生烃的热解过程和烃类运移的动力学过程。平落坝气田中侏罗统气藏的烃类大部份形成于烃源岩低成熟和成熟的早期阶段并受到晚期成熟气体的不断补给。平落坝和大兴西气田多数气藏的烃类被认为是从源区垂直向上运移通过上伏地层而进入气藏的，白马庙气田的烃类被认为是沿断裂通道向上侏罗统气藏聚集的。平落坝和大兴西气田的δ^13Cco2值有很宽的分布范围(-10.7‰～-0.7‰)，这表明气田的CO2由来自基底的海洋碳酸盐岩无机碳成份和沉积地层的有机碳成份混合而成。这些气田的[He／CH4]-[N2／CH4]值之间和δ^13Cco2-δ^13Cc1值之间的相关性表明，非烃气体在进入气藏前已同烃类很好地混合，并被CH4为主流相的气流携带着向气藏运移。  相似文献   

Measurements of Trace Gases in the Inflow of South China Sea Background Air and Outflow of Regional Pollution at Tai O, Southern China     

T. Wang  H. Guo  D. R. Blake  Y. H. Kwok  I. J. Simpson  Y. S. Li 《Journal of Atmospheric Chemistry》2005,52(3):295-317

We present a 16-month record of ozone (O₃), carbon monoxide (CO), total reactive nitrogen (NO_y), sulphur dioxide (SO₂), methane (CH₄), C₂ – C₈ non-methane hydrocarbons (NMHCs), C₁ – C₂ halocarbons, and dimethyl sulfide (DMS) measured at a southern China coastal site. The study aimed to establish/update seasonal profiles of chemically active trace gases and pollution tracers in subtropical Asia and to characterize the composition of the `background' atmosphere over the South China Sea (SCS) and of pollution outflow from the industrialized Pearl River Delta (PRD) region and southern China. Most of the measured trace gases of anthropogenic origin exhibited a winter maximum and a summer minimum, while O₃ showed a maximum in autumn which is in contrast to the seasonal behavior of O₃ in rural eastern China and in many mid-latitude remote locations in the western Pacific. The data were segregated into two groups representing the SCS background air and the outflow of regional continental pollution (PRD plus southern China), based on CO mixing ratios and meteorological conditions. NMHCs and halocarbon data were further analyzed to examine the relationships between their variability and atmospheric lifetime and to elucidate the extent of atmospheric processing in the sampled air parcels. The trace gas variability (S) versus lifetime (τ) relationship, defined by the power law, S_lnx = Aτ^{− b}, (where X is the trace gas mixing ratio) gives a fit parameter A of 1.39 and exponent b of 0.42 for SCS air, and A of 2.86 and b of 0.31 for the regional continental air masses. An examination of ln[n-butane]/ln[ethane] versus ln[propane]/ln[ethane] indicates that their relative abundance was dominated by mixing as opposed to photochemistry in both SCS and regional outflow air masses. The very low ratios of ethyne/CO, propane/ethane and toluene/benzene suggest that the SCS air mass has undergone intense atmospheric processing since these gases were released into the atmosphere. Compared to the results from other polluted rural sites and from urban areas, the large values of these species in the outflow of PRD/southern China suggest source(s) emitting higher levels of ethyne, benzene, and toluene, relative to light alkanes. These chemical characteristics could be unique indicators of anthropogenic emissions from southern China.  相似文献   

A Review of Research on Human Activity Induced Climate ChangeⅠ. Greenhouse Gases and Aerosols     

王明星  刘强  杨昕 《大气科学进展》2004,(3)

Extensive research on the sources and sinks of greenhouse gases, carbon cycle modeling, and the characterization of atmospheric aerosols has been carried out in China during the last 10 years or so. This paper presents the major achievements in the fields of emissions of greenhouse gases from agricultural lands, carbon cycle modeling, the characterization of Asian mineral dust, source identification of the precursors of the tropospheric ozone, and observations of the concentrations of atmospheric organic compounds. Special, more detailed Information on the emissions of methane from rice fields and the physical and chemical characteristics of mineral aerosols are presented.  相似文献   

Natural gas generation model and its response in accumulated fluids in the Yinggehai basin   总被引：2，自引：0，他引：2  

郝芳  邹华耀  黄保家 《中国科学D辑(英文版)》2003,46(11):1103-1112

The generation of natural gases is much more complicated in comparison with liquid petro-leum in that natural gases could be generated from both humic and sapropelic organic matter at different stages and that natural gases could be organic and inorganic …  相似文献   

塔里木盆地中高氮天然气的成因及其与天然气聚集的关系   总被引：2，自引：0，他引：2  

《沉积学报》2000,18(4)

塔里木盆地塔北和塔中地区的海相腐泥型天然气,N2含量较高,尤其是湿气,N2含量分布在10.1％～36.2％,而干气的N2含量则低于10％,即湿气的N2含量高于干气的N2含量。同是下古生界寒武－奥陶系来源的海相腐泥型天然气,为什么湿气和干气的氮气含量相差如此之大?根据与氮气相伴生的烃类气体、非烃气体及稀有气体的组份及同位素特征,认为塔里木盆地的中高氮天然气属于有机成因,来源于下古生界海相烃源岩。文章还提出塔北和塔中地区湿气和干气N2含量差异与源岩的演化程度和圈闭的捕获条件有关。  相似文献   

Sources and sinks of atmospheric methane   总被引：7，自引：0，他引：7  

D. H. Ehhalt  U. Schmidt 《Pure and Applied Geophysics》1978,116(2-3):452-464

In 1972 average mixing ratio of methane in the troposphere was 1.41 ppm and 1.3 ppmv for the northern and southern hemisphere, respectively, which corresponds to a total amount of 4×10¹⁵ g of CH₄ present in the atmosphere. Most is of recent biologic origin.¹⁴C analyses show that no more than 20 percent is released by fossil sources. The various ecosystems producing CH₄ are discussed and the total annual production is estimated to lie between 5.5×10¹⁴ g/yr and 11×10¹⁴ g/yr. The corresponding turnover times for atmospheric CH₄ range from 4 to 7 yrs. The destruction of CH₄ takes place mainly in the troposphere, most probably through the reaction of CH₄ + OH CH₃ + H₂O. About 10 percent of the CH₄ is destroyed in the stratosphere. The CH₄ cycle contributes on the order of 1 percent to the atmospheric carbon cycle.  相似文献