一种获取包裹体内压的新方法——二氧化碳拉曼光谱法

对CO2的拉曼光谱特征做了介绍，特别指出了CO2费米共振峰随温度和压力的变化特点。利用CO2费米共振峰与密度的关系，结合状态方程对山东昌乐一临朐地区的火山岩包裹体进行了研究，获得了该地区火山岩包裹体的现实内压。结果表明，该地区包裹体的现实内压主要集中在5．75—18．29MPa。简单恢复了包裹体的形成深度，经与前人研究成果对比，显示该方法具有一定的可靠性。这种方法可以作为获取合CO2包裹体内压的一种新方法。     

温室气体源汇及其对气候影响的研究现状

温室气体对全球气候变化将产生深远的影响。本文拟从温室气体源汇研究以及温室气体对气候环境的影响等方面论述温室气体研究进展。尽管目前国内外对主要的温室气体源与汇研究报道很多,但不同的研究结果不尽一致,有些研究间甚至出现相反的结论。温室气体增加对气候的影响及其检测,主要是利用不同复杂程度的数值模式进行研究。     

Diffuse Emission of CO2 from Showa-Shinzan, Hokkaido, Japan: A Sign of Volcanic Dome Degassing

Two soil CO₂ efflux surveys were carried out in September 1999 and June 2002 to study the spatial distribution of diffuse CO₂ degassing and estimate the total CO₂ output from Showa-Shinzan volcanic dome, Japan. Seventy-six and 81 measurements of CO₂ efflux were performed in 1999 and 2002, respectively, covering most of Showa-Shinzan volcano. Soil CO₂ efflux data showed a wide range of values up to 552 g m^-2 d^-1. Carbon isotope signatures of the soil CO₂ ranged from -0.9‰ to -30.9‰, suggesting a mixing between different carbon reservoirs. Most of the study area showed CO₂ efflux background values during the 1999 and 2002 surveys (B = 8.2 and 4.4 g m^-2 d^-1, respectively). The spatial distribution of CO₂ efflux anomalies for both surveys showed a good correlation with the soil temperature, indicating a similar origin for the extensive soil degassing generated by condensation processes and fluids discharged by the fumarolic system of Showa-Shinzan. The total diffuse CO₂ output of Showa-Shinzan was estimated to be about 14.0–15.6 t d^-1 of CO₂ for an area of 0.53 km².     

爆裂法作为快速测定流体包裹体中二氧化碳（和其它气体）含量的手段及其在勘探中的使用：以中国山东和河北省金矿为例

The acoustic decrepitation method heats a small monomineralic sample and counts pressure impulses as the inclusions burst when they develop high internal pressures.For aqueous fluids,the decrepitation temperature is correlated with the homogenisation temperature,but gas rich fluids give a distinct and characteristic low temperature decrepitation peak which can be used to recognize gas rich fluid inclusions.This information is useful in exploration for Au deposits,which are frequently associated with CO_2 rich and sometimes CH_4 rich fluids. This distinctive decrepitation occurs because the CO_2 rich inclusion fluids expand according to the gas law and develop internal pressures high enough to burst the host mineral grain at temperatures well below their homogenisation temperatures.In contrast,aqueous fluids condense to a liquid and vapour phase during post-entrapment cooling.Upon subsequent heating their internal pressures do not increase significantly until after homogenisation to a single phase occurs and hence they do not decrepitate"prematurely"as gas rich inclusions do. This behaviour is usually regarded as an annoyance in conventional microthermometric homogenisation studies,but can readily be used as an exploration aid to find mineralisation deposited from such gas rich fluids.Decrepitation results on samples from Cowra Ck, NSW,Australia,which have also been microthermometrically measured for CO_2 content,show that amounts of less than 5 mole % CO_2 are easily distinguished by decrepitation and amounts as low as 1 mole % CO_2 may be determinable. Examples of the use of acoustic decrepitation in the study of 6 gold mines in the Shandong and Hebei provinces of China are discussed.     

Tilt corrections over complex terrain and their implication for CO<Subscript>2</Subscript> transport

Observational data from sonic anemometers are commonly rotated from sonic to streamline coordinates, a procedure that is called tilt correction. Tilt corrections are often used to post-process air velocity data collected from sonic anemometers to allow objective interpretation of air flow data relative to the Earth. Since streamline coordinates depend on dynamical characteristics of the flow, the tilt correction depends not only on temporal and spatial variations of the flow, but also on local circulations. We found that ensemble- averaged slope flows are approximately parallel to the terrain slope close to the ground within the canopy layer, but not above, due to the influence of the diurnal variation of local vertical circulations. As a result, the diurnal variation of the observed vertical velocity in streamline coordinates at 21.5 m above the ground over 11-m tall forest canopies can be opposite to that calculated from the continuity equation. To estimate CO₂ transport over sloping terrain, a workable reference coordinate system is needed such that multiple sonic anemometers have a common reference relative to the Earth. Streamline coordinate systems can be the choice of the common reference coordinate system only if flow, at least ensemble-averaged flow, is parallel to terrain slopes. The choice of the reference coordinate system and its implication in investigation of CO₂ transport are discussed. The National Center for Atmospheric Research is sponsored by the National Science Foundation.     

The Atmospheric Oxidation of the HS Radical: Reaction with NO2

The atmospheric reaction between HS and NO₂ was theoretically investigated at 298 K and 1 atm of pressure. Our results show that the first reaction step will lead to the formation of HSNO₂ or HSONO, spontaneously and exothermically. HSONO easily decomposes into HSO + NO. On the other hand, HSNO₂ can hardly dissociate in the reactants, and its isomerization to other adducts is much hindered. Production of HNO + SO and SNO + OH was found to be unfavorable. Thus, the main products would be HSO + NO and HSNO₂, and new investigations focusing on the atmospheric fate of HSNO₂ are suggested. A general discussion of the fate of HS under atmospheric conditions is presented. Recent investigations indicate that NO₂, O₂ and N₂O should be the most important oxidants of HS, while the O₃ influence will not be significant.     

岩溶发育对温室气体CO2的调节能力研究

温室效应是当今世界上许多国家及其政府关注的重要问题之一。从地质角度研究全球最大碳库－－碳酸盐岩在其岩溶发育过程中对温室气体ＣＯ２的调节能力,从而为更全面,定量地考察温室气体ＣＯ２循环提供新思路及依据。     

Measurements of Reaction Coefficients of NO2 and HONO on Aerosol Particles

The reaction coefficients of nitrogen dioxide and nitrous acid with monodisperse sodium chloride and ammonium sulphate aerosols have been measured in a flow reactor at atmospheric pressure. These experiments were performed at relative humidities above and below the deliquescence points of both aerosols (r.h. 50 and 85%) at 279 K. The results for NO₂ afford a reaction coefficient in the range (2.8–10) × 10^-4 and for HONO, (2.8–4.6) × 10^-3. For both species, there appears to be an enhancement of the reaction coefficient on sodium chloride aerosol at 50% r.h. The results are compared with reaction coefficients determined by other experimental methods. A good agreement is found for both gases between this method and the coated denuder method previously developed in our research laboratories (Msibi et al., 1993) and with the majority of other published data for NO₂. In the case of HONO, our estimate of reaction coefficient is smaller than, or at the lower limits of the ranges reported by other published studies.     

The ocean as source or sink of reactive trace-gases

Summary After a brief review on recent experimental work on the uptake resp release of SO₂ and NH₃ by the ocean, new results on the distribution of these reactive trace-gases in the marine atmosphere are presented. In the case of SO₂ there is no doubt that the ocean acts as a sink. In the case of NH₃ new observations and calculations show that under certain conditions the ocean may be a NH₃ source.     

碳纳米管和纳米二氧化钛复合光催化剂处理海洋柴油污染的研究

利用溶胶凝胶法自制了碳纳米管和纳米二氧化钛的复合光催化剂,采用投射电子显微镜和X光衍射仪对粉体的粒径、物象、形貌和热稳定性等进行表征。通过研究光照条件、催化剂的投加量、油的初始浓度、催化剂制备的煅烧条件等因素,考察了自制碳纳米管和纳米二氧化钛的复合催化剂对降解模拟海洋柴油污染的海水去除率的影响。研究发现,在可见光照条件下,400℃煅烧2 h的复合催化剂,投加量为0.4 g/L、柴油的初始浓度为0.6 g/L、反应的光照时间为4 h时效果最好,去除率可达到67.65%。