瓦里关大气降水的化学特征

利用2007—2009年瓦里关本底台降水化学观测资料,分析了瓦里关降水的pH值、电导率及Cl-、NO-3、SO2-4、NH+4、K+、Na+、Ca2+、Mg2+等离子成分的分布特征。结果表明,瓦里关pH值和电导率的年平均值分别为6.60和21.26μs/cm,2007—2009年呈逐年升高趋势。根据pH值,瓦里关降水以中性降水为主,占总降水的65.13%,其次为碱性降水,酸雨最少。离子浓度大小排序依次为Ca2+SO2-4Na+NH+4Cl-Mg2+NO-3K+,且存在明显的季节变化特征,K+、Na+、Ca2+、Mg2+有相似的来源。瓦里关降水中SO2-4/NO3-的范围为0.35~16.48,平均值为3.07;2007—2009年SO2-4/NO-3值呈逐年下降趋势;SO2-4/NO-3全年存在两个峰值,分别在4月和9—10月。     

苏南三市秋冬季PM2.5中水溶性离子和元素特征及源解析

2010年11月16日至12月17日在南京、常州、苏州三城市设置采样点,24 h采集大气PM_2.5样品,并测定其水溶性无机离子和元素的浓度,在此基础上讨论PM_2.5及无机组分的时空分布特征。结果表明,采样期间,PM_2.5污染较严重,且苏州最重,常州次之,南京最轻,南京、苏州、常州日均浓度分别是国家二级标准(75 μg/m³)的1.44、2.32、1.53倍;三市PM_2.5离子组分中,阴离子均以SO₄^2-和NO₃^-为主,阳离子以Ca²⁺和Mg²⁺为主;苏州Na⁺和Cl^-之间的相关性较高,其受到海盐输送影响较大;三城市PM_2.5中Ca是最主要元素,Al次之。运用主成分法分析南京、常州和苏州PM_2.5的来源可知,三城市PM_2.5受多个污染源影响,包括生物质燃烧、地表扬尘、五金工业及汽车尾气排放等。     

Determination of dissolved organic matter in streamwater using visible spectrophotometry: A comment

A discussion querying the need (Grieve, 1985) for further studies on the use of the technique, which is already well established. The use of chemical oxygen demand is also questioned.     

塔里木盆地满加尔坳陷的演化过程及石油地质特征

以盆地演化为背景，将满加尔坳陷的盖层演化过程划分为三大构造旋回、五个演化阶段：１．震旦－泥盆纪克拉通盆地旋回，２．石炭－二叠纪类前陆盆地旋回，３．中新生代前陆盆地和再生前陆盆地旋回；①震旦纪－早奥陶世克拉通裂解伸展阶段，②中奥陶世－泥盆纪挤压挠曲盆地阶段，③石炭－二叠纪克拉通内坳陷盆地阶段；④三叠－侏罗纪前陆盆地阶段，⑤白垩纪－新生代再生前陆盆地阶段．通过对“三套两类”生油岩（寒武－奥陶系、石炭系、三叠－侏罗系）及局部构造特征的研究，认为满加尔坳陷是烃类的生成供给区，而不是烃类聚集成藏的有利地区。油气勘探的重点是南、北及西侧斜坡地带的地层圈闭。     

Influence of high-fluorine environmental background on crops and human health in hot spring-type fluorosis-diseased areas

Drinking water-type fluorosis is the most harmful endemic disease in China with the largest number of sufferers. Although the implementation of the policy to alter water sources to lower fluoride level has effectively controlled the spread of this kind of endemic disease, its prevalence could not thoroughly be stopped because the high-fluoride environmental background in these endemically diseased areas could still do harm to human health through food chain. Therefore, it is necessary to conduct a more deep-going study on the drinking water-type fluorosis. To investigate the effect of high fluorine environmental background on crops and human health in the hot spring-type fluorosis-diseased areas, local water, paddy soil, rice, whole vegetables and soils around their roots were sampled for analysis. The results were compared with those of the control groups in fluorosis-free areas which are similar to the fluorosis-diseased areas both in natural background and in social background. It is indicated that rice and vegetables can accumulate water-soluble fluorine either in soils or in irrigating water, and different crops have different abilities of fixing fluorine. The contents of fluorine in different parts of vegetables in the fluorosis-diseased and fluorosis-free areas were statistically categorized. The results showed that the fluorine contents of roots, tubers, leaves and flowers of vegetables in the fluorosis-diseased areas are 3.56, 1.17, 3.07 and 3.23 mg/kg, respectively. However, comparisons showed that in the fluorosis-free areas, the fluorine contents are 2.17, 0.70, 1.91 and 2.52 mg/kg, respectively. Moreover, different parts of a crop also show significantly different fluorine fixation abilities. It is demonstrated that the fluorine contents of the strongly metabolic parts are relatively high. For example, the fluofine contents of roots, leaves and flowers of vegetables are much higher than those of stems. The fluorine fixation ability of seeds is very weak. In order to reduce the risk of human body＇s     

陕西渭河盆地氦气资源赋存状态及其意义

氦气资源是一种稀有紧缺性战略资源。渭河盆地具有良好的氦气资源显示,前人认为区内氦气及伴生气资源为水溶气。通过已有石油井、地热井录井、样品测试、动态监测等资料分析,认为渭河盆地不仅存在水溶气资源,也存在游离态氦及伴生气资源,即具有富氦天然气层（藏）,这一认识对进一步的氦气资源评价与开发利用具有重要意义。     

陆相湖盆沉积有机质富集机理研究进展

有机质富集机理的研究对于寻找优质烃源岩、评价盆地的含油气远景具有重要的意义,尤其在日益受到人们重视的页岩气、致密气、油页岩等非常规资源的勘探开发影响下,其研究就显得愈来愈重要和紧迫。而有机质富集机理总体研究程度并不高,对于陆相湖盆有机质的研究相对更为薄弱。以陆相湖盆为研究对象,开展大量国内外关于有机质富集机理的调研,从有机质的生产、有机质分解与保存、有机质的稀释作用三个方面系统总结了陆相湖盆有机质富集的控制因素,并对湖泊与海洋有机质形成的差异性进行了对比分析。研究表明,湖盆有机质的生产受地区光照率、营养盐供给、湖盆地貌、气候环境、湖泊水介质条件、藻类季节性勃发、自养型细菌等的影响;有机质分解与保存受水体分层、细菌生物、无机矿物、水介质条件、黏土矿物、沉积速率等的影响;有机质的稀释作用受沉积速率的影响,并最终得出湖盆中有机质的含量实际上是“有机质生产-有机质分解-有机质稀释”三者相互作用的结果。提出今后值得进一步关注和亟待深入研究的两个方向:自养型细菌在何种环境条件下可以创造高有机质生产力以及不同的水介质条件对有机质分解与保存的影响。     

Mercury,Trace Elements and Organic Constituents in Atmospheric Fine Particulate Matter,Shenandoah National Park,Virginia, USA: A Combined Approach to Sampling and Analysis

Compliance with U.S. air quality regulatory standards for atmospheric fine particulate matter (PM_2.5) is based on meeting average 24 hour (35 μ m^?3) and yearly (15 μg m^?3) mass‐per‐unit‐volume limits, regardless of PM_2.5 composition. Whereas this presents a workable regulatory framework, information on particle composition is needed to assess the fate and transport of PM_2.5 and determine potential environmental/human health impacts. To address these important non‐regulatory issues an integrated approach is generally used that includes (1) field sampling of atmospheric particulate matter on filter media, using a size‐limiting cyclone, or with no particle‐size limitation; and (2) chemical extraction of exposed filters and analysis of separate particulate‐bound fractions for total mercury, trace elements and organic constituents, utilising different USGS laboratories optimised for quantitative analysis of these substances. This combination of sampling and analysis allowed for a more detailed interpretation of PM_2.5 sources and potential effects, compared to measurements of PM_2.5 abundance alone. Results obtained using this combined approach are presented for a 2006 air sampling campaign in Shenandoah National Park (Virginia, USA) to assess sources of atmospheric contaminants and their potential impact on air quality in the Park. PM_2.5 was collected at two sampling sites (Big Meadows and Pinnacles) separated by 13.6 km. At both sites, element concentrations in PM₂₅ were low, consistent with remote or rural locations. However, element/Zr crustal abundance enrichment factors greater than 10, indicating anthropogenic input, were found for Hg, Se, S, Sb, Cd, Pb, Mo, Zn and Cu, listed in decreasing order of enrichment. Principal component analysis showed that four element associations accounted for 84% of the PM_2.5 trace element variation; these associations are interpreted to represent: (1) crustal sources (Al, REE); (2) coal combustion (Se, Sb), (3) metal production and/or mobile sources (Mo, Cd, Pb, Cu, Zn) and (4) a transient marine source (Sr, Mg). Concentrations of Hg in PM_2.5 at background levels in the single pg m^?3 were shown by collection and analysis of PM_2.5 on filters and by an automated speciation analyser set up at the Big Meadows air quality site. The speciation unit revealed periodic elevation of reactive gaseous mercury (RGM) that co‐occurred with peaks in SO₂, indicating an anthropogenic source. GC/MS total ion current chromatograms for the two sites were quite similar indicating that organic signatures were regional in extent and/or that the same compounds were present locally at each site. Calculated carbon preference index values for n‐alkanes indicated that plant waxes rather than anthropogenic sources, were the dominant alkane source. Polycyclic aromatic hydrocarbons (PAHs) were detected, with a predominance of non‐alkylated, and higher molecular weight PAHs in this fraction, suggestive of a combustion source (fossil fuel or forest fires).     

固市凹陷非常规水溶甲烷气成因及来源

针对渭河盆地固市凹陷水溶甲烷气的成因类型进行分析研究。对地层水溶甲烷气碳同位素δ13C₁及重烃的含量研究发现,不同层位的水溶甲烷气成因类型不同。新近系张家坡组水溶甲烷气主要为有机成因的生物气,来源于本层含碳质较高的灰黑色泥灰岩生物分解,为自生自储式;下部蓝田—灞河组水溶甲烷气以未成熟的煤型热解气（煤型腐殖型）为主,来源于下部地层。对CO₂碳同位素的分布范围和含量进行分析得出,δ13C_CO2 < -10‰,为典型的壳源型有机成因,证明蓝田—灞河组水溶甲烷气和CO₂来源于下部地层的混合型气,结合乙烷碳同位素分析,得出下部地层可能存在有机成因的煤型热解气层系。      

On-line measurement of water-soluble ions in ambient particles

Combining the system of rapid collection of ambient particles and ion chromatography, the system of rapid collection of fine particles and ion chromatography (RCFP-IC) was established to automatically analyze on-line the concentrations of water-soluble ions in ambient particles. Here, the general scheme of RCFP-IC is described and its basic performance is tested. The detection limit of RCFP-IC for SO2? 4 , NO?3 , NO?2 , Cl? and F? is below 0.3 μg m?3. The collection efficiency of RCFP-IC increases rapidly with increasing sized particles. For particles larger than 300 nm, the collection efficiency approaches 100%. The precision of RCFP-IC is more than 90% over 28 repetitions. The response of RCFP-IC is very sensitive and no obvious cross-pollution is found during measurement. A comparison of RCFP-IC with an integrated filter measurement indicates that the measurement of RCFP-IC is comparable in both laboratory experiments and field observations. The results of the field experiment prove that RCFP-IC is an effective on-line monitoring system and is helpful in source apportionment and pollution episode monitoring.