塔里木盆地东部地区天然气地球化学特征及成因探讨(之二)

天然气的组分和碳、氢同位素组成特征研究表明塔里木盆地已发现的天然气均为热解气。通过气源对比可知,该盆地东部地区的天然气主要有两种类型 :1)是来自震旦纪到下古生界海相腐泥型母质的油型气,其甲烷、乙烷、丙烷δ13C值,分别为-44.5‰～-33.8‰、- 42‰～-2 8.1‰和-35.4‰～-2 8.4‰,其甲烷的氢同位素组成大于- 2 0 0‰;2 )是产自中生代陆相腐殖型源岩的煤型气,其甲烷、乙烷、丙烷的δ13C值分别为-40.5‰～-33.1‰、- 2 9.7‰～-2 1.3‰和-2 6.3‰～-2 0.3‰,其甲烷的氢同位素组成小于-2 0 0‰。将天然气的地化特征与地质背景相结合判断可知,在塔北隆起地区一些天然气藏是由成熟 (高成熟 )阶段的油型气与过成熟阶段的油型气混合形成,另一些天然气藏是由成熟阶段的油型气和成熟阶段的煤型气混合形成.     

老挝龙湖钾盐矿床沉积碳酸盐碳、氧同位素组成及其对成钾环境的初步指示

碳、氧同位素作为反映古沉积环境、成矿物源和水–岩反应等良好的稳定同位素指标,被广泛应用。通过对老挝龙湖钾盐矿区ZK309、ZK301、ZK311和ZK004四个钻孔农波组盐岩上覆泥岩碳、氧同位素组成的分析,讨论了盐岩上覆泥岩沉积的碳、氧同位素组成变化特征及其指示的沉积环境。经分析,所测碳、氧同位素基本代表了碳酸盐碳、氧同位素组成,初步推测这些碳酸盐均为当地自生,受后期改变很少,δ13C和δ18O平均值分别为-5.1‰和-4.6‰,其中δ13C值略高于一般陆相碳酸盐碳同位素最大值–5.69‰,δ18O值介于–2.71‰~–10.8‰之间,ZK309和ZK301钻孔碳、氧同位素相关系数均小于0.7,初步指示盐岩沉积之后沉积环境为陆相。δ13C值略高于–5.69‰,推测是后期盐岩层被淋滤,泥岩层受淋滤后的残余卤水影响的结果,这也解释了蒸发岩沉积层序异常(钾石盐覆盖于光卤石之上)的沉积特征。因此,在本研究中,大气水在泥岩碳、氧同位素的变化中扮演了重要角色。     

水中氯代烃单体碳同位素分析中预富集方法进展

高精度准确测定氯代烃单体碳同位素对示踪污染物来源,了解污染物的生物降解过程具有重要意义。在环境转化过程中,有机污染物的同位素组成可能是稳定不变的,也有可能发生改变。若污染物的同位素组成在迁移转化过程中不变,根据其同位素组成可以示踪污染物的来源;若同位素组成变化,根据同位素分馏结果,可以评价环境中有机污染物降解发生的可能性和程度。本文综述了固相微萃取、静态顶空进样、吹扫-捕集、多级串联技术等前处理方法与气相色谱-燃烧-同位素比值质谱仪(GC-C-IRMS)联用分析水中氯代烃单体碳同位素的研究进展,比较了分析方法的优缺点。液-液萃取较少用于水中氯代烃的单体同位素分析。静态顶空进样、固相微萃取、吹扫-捕集都是无溶剂富集技术,与GC-C-IRMS联用分析水中氯代烃单体同位素过程中不存在或存在小且恒定的可校正的同位素分馏,分析精度一般优于1‰,没有二次污染,降低了杂质干扰,提高了GC-C-IRMS的分辨率和分析精度,降低了检测限。从静态顶空进样、固相微萃取、吹扫-捕集,到多级串联等技术与GC-C-IRMS联用分析水中氯代烃单体同位素比值,检测限逐渐降低。目前,吹扫-捕集-GC-C-IRMS在分析水中氯代烃中应用最广泛,重现性好、检测限低。针内微萃取、管内微萃取、搅动棒吸附萃取和顶空进样吸附萃取等前处理方法与GC-C-IRMS仪联用具有一定的应用前景。     

柴达木盆地西部地区咸化湖盆天然气地球化学特征及成因类型判识指标——以古近系—新近系为例

根据天然气地球化学基本理论,对柴达木盆地西部（柴西）地区天然气的地球化学特征进行分析。测试和收集该地区18个油气田及含油气构造的83个天然气样品,分析其组分和C同位素数据,结果显示,该区天然气以烃类气体为主,烃类含量介于79.24%~99.81%之间,天然气比重介于0.72~1.36之间,天然气干燥系数（C1/C2+）介于1.04~617.8之间,甲烷C同位素值介于-51.4‰~-24.2‰之间,乙烷C同位素值介于-34.2‰~-17.4‰之间。在此基础上,对该区不同构造带的天然气成因类型进行研究。研究结果表明,柴达木盆地西部地区天然气类型可划分为腐泥型气、腐殖型气、混合气3类,柴西北部天然气主要为腐泥型气和混合气,少量腐殖型气;柴西南部主要为腐泥型气,少量混合气。同时,建立了天然气成因类型的判识指标,对该区的天然气地球化学特征有了较为深入的认识,对今后的天然气勘探具有指导意义。     

Detection of petroleum contamination in river sediments from Quebec City region using GC–IRMS

Isotopic analysis by compound specific gas chromatography–isotope ratio mass spectrometry (GC–IRMS) is used to detect and characterize petroleum pollution in surficial sediments along the St Lawrence River, near Quebec City. Unusually mature n-alkane distributions have been found in some recent intertidal sediments in the region. GC–IRMS results suggest that the n-alkanes are not derived from indigenous organic sources because they carry δ¹³C values between −30.0 and −27.0‰, as well as very small isotopic differences between odd and even numbered n-alkanes, which are both typically associated with petroleum products. Comparison of these sediments with bunker fuel, an oil used in the shipping industry, has shown a close isotopic correlation in some sites, which is further supported by biomarkers. Overall, the contamination has been dispersed along the river but is generally localized around the industrial region where hydrocarbon transfer from shore storage to ships takes place. This study illustrates how GC–IRMS can be used effectively in the detection and characterization of petroleum pollutants in sediments.     

塔里木盆地克拉通区天然气碳同位素与成熟度关系探讨

气藏中天然气碳同位素的轻重不仅反映了母质继续效应和成熟效应,同时也取决于累积、散失、混合效应。塔里木盆地３个古隆起（中、 塔北和巴楚）区的天然气均主要来自寒武系一下奥陶统烃财。塔中地区保存条件好,天然气聚集时期长,为连续聚气区,其累积效应强,碳同位素普遍偏轻;塔北和 扎塔格地区保存状况相对较差,天然气聚集期短,累积效应弱,碳同位素值重了区。塔中北皮一些奥陶第 藏由于有中上奥陶统生成的低熟气－生物气     

A numerical study of tropospheric ozone in the springtime in East Asia

The Models-3 Community Multi-scale Air Quality modeling system (CMAQ)coupled with the Regional Atmospheric Modeling System (RAMS)is applied to East Asia to study the transport and photochemical transformation of tropospheric ozone in March 1998．The calculated mixing ratios of ozone and carbon monoxide are compared with ground 1evel observations at three remote sites in Japan and it is found that the model reproduces the observed features very well．Examination of several high episodes of ozone and carbon monoxide indicates that these elevated levels are found in association with continental outflow,demonstrating the critical role of the rapid transport of carbon monoxide and other ozone precursors from the continental boundary layer．In comparison with available ozonesonde data,it is found that the model-calculated ozone concentrations are generally in good agreement with the measurements,and the stratospheric contribution to surface ozone mixing ratios is quite limited．     

Climatology of Ozone, PAN, CO, and NMHC in the Free Troposphere Over the Southern North Atlantic

Free tropospheric measurements of ozone, peroxyacetylnitrate andprecursors (CO, NMHC) that were made within the framework of the EUROTRACsub-project TOR (Tropospheric Ozone Research) between 1990 and 1995 at theGAW station Izana, Tenerife (28°18N, 16°30W) arediscussed. The average annual cycles reveal the importance of transport fromnorthern mid-latitudes and the role of photo-chemistry. According toair-mass trajectories, which were supplied to us from AEROCE(Atmosphere/Ocean Chemistry Experiment), transport from northernmid-latitudes is associated with high precursor concentrations in winter,whereas ozone concentrations in winter are not much influenced by transportpatterns, suggesting a rather uniform distribution over the northern part ofthe Northern Hemisphere around mean value of 43 ± 5 ppb. In summer,high ozone concentrations of up to 90 ppb are often encountered duringtransport from north, while the levels of precursors are much lower than inwinter, because of photochemical destruction. Trajectories from southerlylatitudes and the Sahara usually have the lowest ozone concentrationsassociated with them.     

Changes in Water Use Efficiency Caused by Climate Change,CO2 Fertilization,and Land Use Changes on the Tibetan Plateau

Terrestrial ecosystem water use efficiency(WUE) is an important indicator for coupling plant photosynthesis and transpiration, and is also a key factor linking the carbon and water cycles between the land and atmosphere. However,under the combination of climate change and human intervention, the change in WUE is still unclear, especially on the Tibetan Plateau(TP). Therefore, satellite remote sensing data and process-based terrestrial biosphere models(TBMs) are used in this study to investigate ...     

太湖入湖河口和开敞区CDOM吸收和三维荧光特征

应用吸收和三维荧光光谱对2007年夏季太湖入湖河口和大太湖开敞区有色可溶性有机物(CDOM)浓度及来源进行研究.结果表明,河口区和开敞区CDOM吸收系数a(355)存在显著空间差异,河口区明显大于开敞(ANOVA,P<0.001),a(355)最大值出现在大浦河口和竺山湾漕桥河几附近,最小值出现在东太湖和胥口湾.a(355)与溶解性有机碳、化学耗氧量浓度存在显著正相关.所有样品一般都含有4个明显的荧光峰,包括1个可见光区的类腐殖质荧光C峰,1个紫外光区的类腐殖酸荧光A峰,2个类蛋白荧光B峰和D峰.河口区外源输入的类腐殖质荧光非常强,最著大于开敞区(ANOVA,P<0.05).而河口区和开敞区类蛋白荧光没有显著性差异,反映开敞区除外源河流输入外,内源生物降解等对类蛋白荧光贡献增加.在河口区B、C峰的比值r(B/C)/b于1,均值为0.62±0.14、在开敞区r(B/C)除12#是0.92,其他值均大于1,均值为1.12±0.13,初步判断r(B/C)可以作为区分CDOM来源的重要参数.CDOM吸收a(355)与类腐殖质荧光C峰、A峰均存在极显著的正相关,而与类蛋白荧光相关性则明显下降,与D峰存在显著正相关,与B峰没有显著相关.