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1.
《Applied Geochemistry》1997,12(3):229-241
The fluorescence spectra of crude oils, synthesized as hydrocarbon fluid inclusions (hcfi) in NaCI crystals, have been recorded and correlated with crude oil chemical analysis. The crude oils represent a wide range in total hydrocarbons, saturate and aromatic fractions, and resin-asphaltene concentration. The fluorescence properties (Lambda max and Q) of the hydrocarbon fluid inclusions display a systematic red shift to longer wavelengths from 440 nm to 595 nm with increasing aromatic content and increasing concentration of NSO-bearing compounds. A positive correlation also exists between Lmax-Q and the thermal maturity parameters nC17/pristane and nC18/phytane. First order linear regression equations provide a method for constraining the chemical composition of natural hydrocarbon fluid inclusions. Lmax and Q correlate positively with oil density (°API), providing for an indirect method of estimating the API of a natural hydrocarbon fluid inclusion assemblage. Fluorescence spectra of non-biodegraded crude oils from the Upper Devonian Birdbear Formation, Saskatchewan, Canada, have been correlated with regionally widespread hcfi within carbonate carrier beds and reservoir rocks of the same formation. The two most dominant types of hcfi spectra match well with the fluorescence spectra from crude oils within the Birdbear Formation. A third, less common population of very-blue fluorescing hcfi (Lmax=415440 nm, Q ≤ 0.10) also occur within fractures, intercrystalfne cements or in fossil overgrowths. The Lmax-Q-API-chemical correlations establised for the synthetic hcfi suggests that the °API of these inclusions is probably > 45° and the saturate/aromatic ratio ranges from 3.2 to 5.1. Spectra from hcfi within quartz overgrowths and cements, fractures and carbonate cements from sandstone reservoirs in the Jeanne d'Arc Basin offshore Newfoundland, compared with fluorescence spectra of crude oils suggests that some of the reservoirs may have been filled by a relatively low maturity oil and then a higher maturity oil. This is reflected in the intermediate spectra of the crude oils relative to the spectra of two separate hcfi events. Other reservoirs appear to have been charged with a relatively high gravity oil which was later biodegraded. This is marked by a blue region spectra for the hcfi compared with a red-shifted spectra for the crude oil (°API = 19). The API of the original unaltered oil which charged the reservoir is estimated to be between 32 and 38° using the Lmax-Q-API relationship established for the synthetic hcfi.  相似文献   

2.
In this study,12 crude oil samples were collected and analyzed from the Ordovician reservoir in the Halahatang Depression,Tarim Basin,China.Although the density of oil samples varies considerably,based on saturated hydrocarbon gas chromatographic(GC),saturated and aromatic hydrocarbon gas chromatographic-mass spectrometric(GC/MS) and stable carbon isotopic composition analyses,all the samples are interpreted to represent a single oil population with similar characteristics in a source bed or a source kitchen,organic facies and even in oil charge history.The co-existence of a full suite of n-alkanes and acyclic isoprenoids with UCM and 25-norhopanes in the crude oil samples indicates mixing of biodegraded oil with fresher non-biodegraded oil in the Ordovician reservoir.Moreover,according to the conversion diagram of double filling ratios for subsurface mixed crude oils,biodegraded/non-biodegraded oil ratios were determined as in the range from 58/42 to 4/96.Based on oil density and oil mix ratio,the oils can be divided into two groups:Group 1,with specific density>0.88(g/cm3) and oil mix ratio>1,occurring in the north of the Upper Ordovician Lianglitage and Sangtamu Formation pinchout lines,and Group 2,with specific density<0.88(g/cm3) and oil mix ratio<1,occurring in the south of the pinchout lines.Obviously,Group 2 oils with low densities and being dominated by non-biodegraded oils are better than Group 1 oils with respect to quality.It is suggested that more attention should be paid to the area in the south of the Upper Ordovician Lianglitage and Sangtamu Formation pinchout lines for further exploration.  相似文献   

3.
Gel permeation chromatography (GPC) using a high performance liquid chromatography (HPLC) system was studied for the separation and enrichment of steroid and hopanoid hydrocarbons from crude oil for stable carbon isotope analysis. A crude oil sample was pretreated using silica gel chromatography and 5A molecular sieve to remove polycyclic aromatic hydrocarbons and n-alkanes. The GPC behavior of both the pretreated saturated hydrocarbon fraction of the oil and standard steroid [5α(H), 14α(H), 17α(H) C27–C29 steranes], hopanoid [17α(H) C27 trisnorhopane, 17α(H), 21β(H) C29–C32 hopanes] and triterpenoid [18α(H)-oleanane, gammacerane] mixtures were examined. The results indicate that 17α(H), 21β(H) hopanes as well as steranes could be enriched efficiently using GPC and that they could be obtained without removing n-alkanes from the oil saturated hydrocarbon fraction. The GPC behavior of steroid and triterpenoid hydrocarbons was controlled by molecular size and shape.  相似文献   

4.
致密油分子尺寸及流动性的研究对致密油藏评价及开发具有重要意义.为明确吉木萨尔凹陷芦草沟组致密油的分子尺寸及其对原油流动的影响,综合核磁共振、红外光谱、元素分析和相对分子质量测定等结果,计算了典型井致密油不同馏分段的分子结构参数,采用Chemoffice软件模拟了相应的分子结构.结果显示致密油组分主要集中在350~500℃馏分段,平均分子中含有多环环烷烃和多环芳烃结构,平均分子尺度为1.232~4.026 nm,表明原油分子在纳米孔喉中占有率较高,影响孔喉流动下限.   相似文献   

5.
Although oil cracking has been documented as one of the important sources of gas in many overmature marine sedimentary basins, the chemical and carbon isotopic signatures of gases of this origin are still open to question. In this study a Cambrian crude oil from the central Tarim basin, along with its main separated fractions (saturates, aromatics and asphaltenes), were pyrolyzed in sealed gold tubes to investigate how generated gases vary in chemical and carbon isotopic composition and how this variation would influence the genetic interpretation of oil cracking gas. The results indicate that the gases from cracking of aromatics and asphaltenes are much drier and more enriched in 13C than the gases from the cracking of saturates and crude oil at the same level of thermal maturity. In the experimental run of 20 °C/h, the dryness index of the gases (defined as the volume percentage of C1 in C1–5) from the cracking of saturates ranges from 26.2–90.6% with the methane carbon isotope change ranging from −54.8‰ to −35.5‰, whereas the dryness index is never lower than 60.6% for the gases from the cracking of aromatics with methane carbon isotope ranging from −39.9‰ to −32.2‰. Correspondingly, experimental data for the four samples plot in different areas in diagrams designed to distinguish oil cracking gas from kerogen cracking gas, such as ln(C2/C3) vs. δ13C2–δ13C3 and δ13C1 vs. δ13C2–δ13C3, indicating compositional variability of crude oil could assert an important influence in these diagrams. Therefore it is prudent to bring other geological constraints into consideration to avoid misinterpretation.The kinetic parameters for the bulk generation of C1–5 gas and the methane carbon isotope fractionation extrapolated to geological conditions of 2 °C/Ma and an initial temperature of 50 °C show that the temperatures of C1–5 gas generation from the aromatics and asphaltenes are lower than those from the saturates and crude oil due to their lower activation energies and frequency factors. Generation of C1–5 gases from the aromatics is modeled to be initiated about 122 °C whereas the initiation temperature for the saturates sample is 176 °C. Below 189 °C (EasyRo = 1.8%), the yields of C1–5 gases follow the order: aromatics > asphaltenes > crude oil > saturates. At similar thermal maturity levels, the methane carbon isotopic compositions are significantly different for the four samples, with an order of 13C enrichment: aromatics > asphaltenes > crude oil > saturates, however the difference in methane carbon isotopes becomes smaller with increasing temperature. This indicates that methane carbon isotopic values can be significantly different for gases cracked from oils that are compositionally diverse, especially in the early stage of methane generation.  相似文献   

6.
Biodegradation, one of the most important weathering processes, alters the composition of spilled oil, making it difficult to identify the source of the release and to monitor its fate in the environment. A laboratory experiment was conducted to simulate oil spill weathering process of microbial degradation to investigate compositional changes in a range of source- and weathering-dependent molecular parameters in oil residues, and the conventional diagnostic ratios for oil spill identification were also evaluated. The conventional diagnostic ratios of n-alkane displayed obvious changes after biodegradation, especially for Pr/n-C17 and Ph/n-C18 with relative standard deviation more than 118.84 %, which suggests they are invalid for oil source identification of the middle-serious spill. Many polycyclic aromatic hydrocarbons (PAHs) are more resistant to biodegradation process than their saturated hydrocarbon counterparts, thus making PAHs to be one of the most valuable fingerprinting classes of hydrocarbons for oil identification. Biomarker ratios of hopanes and steranes were also useful for source identification even after moderate biodegradation, and the diagnostic ratios from them could be used in tracking origin and sources of hydrocarbon pollution. Finally, the carbon isotopic type curve may provide another diagnostic means for correlation and differentiation of spilled oils, and be particularly valuable for lighter refined products or severely biodegraded oils, the source of which may be difficult to identify by routine biomarker techniques.  相似文献   

7.
准噶尔盆地YJ油田是一个埋藏很深,成藏机理复杂的岩性、地层圈闭油气藏。通过侏罗系西山窑组和三工河组原油、油砂抽提物地球化学特征分析后认为,西山窑组原油具有两期成藏混合的特征,三工河组成熟轻质原油、油砂抽提物又表现出煤系烃源岩的特征。这表明,YJ油田具有多源多期充注成藏的特点。对地表土壤中甲烷碳同位素、烃类比值、三维荧光图谱的分析后认为,甲烷同位素、甲烃同位素、烃类比值与凝析油伴生气、石油伴生气的经验值相符;三维荧光既有凝析油-轻油又有轻油-重油的图谱特征。这与原油和油砂抽提物的研究结果相近,也表明该油田具有多种油源。因而认为,在未知地区对土壤油气地球化学特征进行研究,对于初步判断油气来源同样具有良好的效果。  相似文献   

8.
生物降解作用对烷基萘异构体分布的影响及其控制因素   总被引：1，自引：0，他引：1  
在受到溢油污染的海滩上采集不同时间序列的石油样品,对芳烃组分烷基萘中的三甲基萘和四甲基萘各异构体的生物降解过程响应进行了详细分析。研究揭示,三甲基萘比四甲基萘更易被生物降解,其中1,2,7-三甲基萘、2,3,6-三甲基萘、2,3,6,7-四甲基萘、1,2,3,7-四甲基萘和1,3,5,7-四甲基萘等异构体具有相对较高的生物降解效率,与最近 Ostojié等利用理论模型计算所给出的降解序列十分一致,进一步证实了烷基萘在表生环境中的降解主要受控于异构体萘环上取代基的数量和位置。研究结果对于表生环境中萘系物类多环芳烃污染的生物修复评价具有重要指导意义。  相似文献   

9.
The biodegradability of polycyclic aromatic hydrocarbons such as naphthalene, fluorene, anthracene and phenanthrene by a halotolerant bacterial consortium isolated from marine environment was investigated. The polycyclic aromatic hydrocarbons degrading bacterial consortium was enriched from mixture saline water samples collected from Chennai (Port of Chennai, salt pan), India. The consortium potently degraded polycyclic aromatic hydrocarbons (> 95%) at 30g/L of sodium chloride concentration in 4 days. The consortium was able to degrade 39 to 45% of different polycyclic hydrocarbons at 60 g/L NaCl concentration. Due to increase in salinity, the percent degradation decreased. To enhance polycyclic aromatic hydrocarbons degradation, yeast extract was added as an additional substrate at 60g/L NaCl concentration. After the addition of yeast extract, the consortium degraded > 74 % of polycyclic aromatic hydrocarbons at 60 g/L NaCl concentration in 4 days. The consortium was also able to degrade PAHs at different concentrations (5, 10, 20, 50 and 100 ppm) with 30 g/L of NaCl concentration. The polycyclic aromatic hydrocarbons degrading halotolerant bacterial consortium consists of three bacterial strains, namely Ochrobactrum sp., Enterobacter cloacae and Stenotrophomonas maltophilia.  相似文献   

10.
非常规油气藏的形成及其分布特征*   总被引：1，自引：0，他引：1       下载免费PDF全文
宋岩  姜林  马行陟 《古地理学报》2013,15(5):605-614
非常规油气领域是目前油气勘探和开发的热点领域, 也是石油工业的发展趋向, 非常规油气的成藏研究对非常规油气勘探具有重要指导意义。非常规油气与常规油气成藏的最本质区别在于非常规油气是非浮力驱动聚集, 这主要是由于致密储集层中微纳米级孔隙发育导致毛细管阻力较大, 同时缺乏提供强大浮力的有利条件。根据烃源岩演化与非常规油气成藏的关系, 将非常规油气资源分为油页岩、页岩油、致密油、页岩气、致密气和煤层气6种类型。油页岩、页岩油、煤层气和页岩气的源储组合特征都是“源储一体”, 而致密油气源储组合有2种类型：一种是源储叠置的临源型致密油气, 另一种是与常规油气藏类似的源储不相临、但距离不远的近源型致密油气。成藏动力学上的差异使非常规油气藏在地质上表现为大面积分布、局部富集、油气赋存具有明显的“滞留”或短距运移特征、没有明显的圈闭边界和无统一的油水界面等特点。  相似文献   

11.
max vs the present depth of the Kupferschiefer, soluble organic matter (SOM) yields, and relative proportions of saturated and aromatic hydrocarbons of the SOM provide evidence for an oxidative alteration of organic matter in highly mineralized Kupferschiefer samples near the Rote F?ule zones. This is confirmed by differences in the composition of the saturated and aromatic hydrocarbon fractions of the soluble organic matter: Saturated hydrocarbons from Rote F?ule samples are dominated by short-chain n-alkanes and higher abundances of pristane and phytane relative to heptadecane (n-C17) and octadecane (n-C18), respectively, compared with samples more distant to the Rote F?ule zone. Compositional changes of the aromatic hydrocarbon fractions with decreasing distance to that zone are characterized by the occurrence of polycyclic aromatic hydrocarbons and elevated ratios of phenanthrene to methylphenanthrenes that are attributed to demethylation reactions and resulted in a decrease of the methylphenanthrene index (MPI 1). Kupferschiefer samples from the barren zone of the Polish Basin do not show these alteration patterns. The observed variations in organic matter composition with burial depth are consistent with changes due to increasing thermal maturation. Maturity assessment is achieved from MPI 1 and the methyldibenzothiophene ratio (MDR). From the relationship between the maturity of organic matter in terms of vitrinite reflectance values and depth of the Kupferschiefer strata, a continuous increase in reflectance of vitrinite is obtained within the Polish Basin. The alteration pattern of organic matter related to base metal mineralization of the Kupferschiefer corresponds to changes in the isotopic composition of organic carbon and calcite. Kerogen within, or close to, Rote F?ule zone is enriched in 13C caused by the preferential release of isotopically light organic compounds through progressive degradation of organic matter. The opposite tendency towards lower δ 13C and δ 18O values of calcite provides evidence for isotopic exchange between carbonate and the oxidizing, ore-bearing solutions and for organic matter remineralization. In contrast, organic matter and calcite from the Kupferschiefer do not show regular trends in δ 13C with increasing thermal maturation. Received: 25 June 1999 / Accepted: 1 December 1999  相似文献   

12.
A series of eight Tertiary coal and carbonaceous shale samples with vitrinite reflectance values between 0.50 and 0.58% were extracted, fractionated and the saturated and aromatic hydrocarbons analysed for characteristic components by GC and GC-MS. Additionally, a microscopical study was undertaken in order to obtain a more precise picture of the samples under investigation.The saturated hydrocarbon fractions displayed the typical n-alkane distribution for coals of this rank, with CPI values between 2.0 and 3.1. Among the branched/cyclic compounds, pristane and α, β-homohopane were recognised as relevant components pointing to an oxic depositional environment. Detection of benzohopanes (C32–C35) in the aromatic hydrocarbon fractions suggests that bacteriohopanetetrol was a significant constituent of the coal biomass. Taking into consideration the Pr/Ph ratios, ash contents and microscopical characteristics of the samples, aspects of the possible degradation of hopanetetrol to homohopane are discussed. Resin-derived diterpenoids with the phyllocladane and kaurane skeleton were tentatively identified and, although minor compounds, they are interpreted to be a sign of the contribution of Podocarpaceae and Araucareaceae to the coal swamp.Aromatic compounds were dominated by alkylnaphthalene derivatives, presumably formed by C-ring cleavage and aromatisation of higher plant-derived pentacyclic triterpenois, which were main components in the high-boiling range of the fractions investigated. Angiosperms (especially Fagaceae) are postulated as source for these polycyclic compounds and, hence, for some of the polyalkylated aromatic bicyclics detected.  相似文献   

13.
The existence of polycyclic aromatic hydrocarbons in the various environments has aroused great environmental concerns due to their potential hazards to human health. The presence of polycyclic aromatic hydrocarbons in aquifer is particularly sensitive where groundwater is used as a source of potable water. Anaerobic biodegradation of polycyclic aromatic hydrocarbons is an attractive option for remediation of contaminated aquifer sediment. Bacterial and archaeal community structures of phenanthrene-degrading aquifer sediment under methanogenic condition were investigated using clone library analysis in combination with microcosm study. The bacterial members were all affiliated with ??-Proteobacteria. Phylum Euryarchaeota was the predominant archaeal group, represented by genera Methanosarcina, Methanobacterium and Thermogymnomonas. Both bacteria (genera Citrobacter and Pseudomonas) and archaea (genus Methanosarcina) might have links to phenanthrene degradation process. This work might provide some new insights into developing strategies for the isolation of the putative polycyclic aromatic hydrocarbons degraders under methanogenic condition and bioremediating polycyclic aromatic hydrocarbons in leachate-contaminated aquifer sediment.  相似文献   

14.
This paper deals with natural temperature records in the heavy (asphaltenes) and the light fractions (C7—light hydrocarbons) of petroleum. Two sets of marine oils formed from different source rocks and petroleum systems were studied using asphaltene kinetics and light hydrocarbon analysis. Both fractions have been reported to contain information about the temperature the respective oils have been exposed to in the subsurface. These indicated temperatures generally correspond to the conditions in the source rock when expulsion occurred. Bulk kinetic analysis of reservoir oil asphaltenes as well as light hydrocarbon (LH) analysis (of dimethylpentanes) were used here in order to evaluate the expulsion temperatures. Surprisingly, when considering information coming from both fractions, an inverse trend between LHs expulsion temperatures (Ctemp) and asphaltenes (Tasph.) can be observed—high Tasph (asphaltene temperatures) occur with low LH Ctemp (light hydrocarbon expulsion temperatures) and low Tasph can be observed when Ctemp is high. These differences are of fundamental importance for the use of such geochemical data in calibrating numerical basin models. The reason for this inverse behaviour is possibly due to the different expulsion behaviour of light hydrocarbons and the heavy fraction of oils, especially when the source rocks contain only moderate amounts of organic matter. In addition it has to be considered that the temperature predictions obtained using asphaltene kinetic analysis are related to the onset temperature of petroleum expulsion, while light hydrocarbons provide, at best, average expulsion temperatures.  相似文献   

15.
中国西北地区面积260×104 km2,已发现100多个油气田,油气资源十分丰富.在几十年的研究和勘探基础上,归纳总结了西北地区压性叠加盆地成油特征:多旋回演化、构造变形七大特性、多时代烃源岩、多套储盖组合、四期成藏、独特油气藏特征和油气分布规律等.   相似文献   

16.
《Chemical Geology》1992,94(4):321-329
Light hydrocarbon and isotope compositions of methane were analyzed in well steam samples from the Matsukawa vapour-dominated type geothermal system. Alkanes (C1-C4) and alkene (C2) were detected in all samples. Light hydrocarbon contents of CO2-type steam are slightly higher than those of CO2-H2S-type steam. The isotope composition of methane and the relationship between methane/ethane ratio and δ13C-value of methane suggest that these light hydrocarbon gases are mixtures of thermogenic and abiogenic components. The abiogenic hydrocarbon may be attributed to magmatic hydrocarbon gases equilibrated with carbon dioxide at fo2 defined by the fayalite-magnetite-quartz buffer (FMQ).  相似文献   

17.
The ecological catastrophe produced by the Prestige oil spill (November 2002) caused severe damage in both North Spanish and French coastal communities. Wild mussel populations of Mytilus galloprovincialis in a zone with marginal introgression of Mytilus edulis were affected at all levels, from high DNA damage to increased polycyclic aromatic hydrocarbon content in tissues. In this article, we describe cytological and population genetic changes of wild mussel populations from the northwestern Iberian coast following the catastrophe. The micronucleus test was employed as an indicator of cytological damage, and the Barcoding mitochondrial cytochrome oxidase I (COI) and the nuclear Glu-5′ genes were analyzed for determining the species and assessing population genetic diversity. Immediate increase of micronuclei counts after the oil spill was found, with a further decrease in consecutive months although the counts did not recover pre-Prestige levels. Reduced variation at mitochondrial sequences in the most exposed areas and reduction of M. edulis traces in the regional genetic pool also suggest long-term impact that may result in evolutionary changes. These results highlight the need of adopting more strict measures in order to prevent this type of accidents and avoid long-term effects on wild populations.  相似文献   

18.
Residual fuel oil spilled into the sea from the Eshkol power station on 8 February, 1998 contaminated about 9 km of the foreshore north of the Ashdod harbour. A study of the aliphatic, polycyclic alkane and polyaromatic hydrocarbon (PAH) composition of the spilled oil shows rapid weathering in the early stages followed by gradual slowdown after about three months. Weathering of isoprenoids and PAH compounds and variation in Pr/Ph ratio appear to occur almost contemporaneously with that of n-alkanes, at a relatively moderate level of degradation, when much of the >C20 n-alkane envelope is still well preserved. Depletion of various compounds in accordance with molecular size rather than molecular structure appears to imply that physical weathering processes, i.e. evaporation and perhaps flushing due to wave energy, might have played an important role in the degradation of the spilled residual fuel oil in this study case.  相似文献   

19.
Basalts interbedded with oil source rocks are discovered frequently in rift basins of eastern China, where CO2 is found in reservoirs around or within basalts, for example in the Binnan reservoir of the Dongying Depression. In the reservoirs, CO2 with heavy carbon isotopic composition (δ13C>-10‰ PDB) is in most cases accounts for 40% of the total gas reserve, and is believed to have resulted from degassing of basaltic magma from the mantle. In their investigations of the Binnan reservoir, the authors suggested that the CO2 would result from interactions between the source rocks and basalts. As the source rocks around basalts are rich in carbonate minerals, volcanic minerals, transition metals and organic matter, during their burial history some of the transition metals were catalyzed on the thermal degradation of organic matter into hydrocarbons and on the decomposition of carbonate minerals into CO2, which was reproduced in thermal simulations of the source rocks with the transition metals (Ni and Co). This kind of CO2 accounts for 55%-85% of the total gas reserve generated in the process of thermal simulation, and its δ13C values range from -11‰- -7.2‰ PDB, which are very similar to those of CO2 found in the Binnan reservoir. The co-generation of CO2 and hydrocarbon gases makes it possible their accumulation together in one trap. In other words, if the CO2 resulted directly from degassing of basaltic magma or was derived from the mantle, it could not be accumulated with hydrocarbon gases because it came into the basin much earlier than hydrocarbon generation and much earlier than trap formation. Therefore, the source rocks around basalts generated hydrocarbons and CO2 simultaneously through catalysis of Co and Ni transition metals, which is useful for the explanation of co-accumulation of hydrocarbon gases and CO2 in rift basins in eastern China.  相似文献   

20.
Stepwise extraction and molecular analysis of non-recoverable oil from intact reservoir core plugs is used to provide constraints on the accumulation history of petroleum in the Permo-Carboniferous Unayzah reservoirs at the Ghazal Field, Saudi Arabia. When integrated with existing tools such as oil geochemistry, gas geochemistry, stable carbon isotopes, fluid inclusions and thermal modeling, the sequential extraction approach helped decode a previously unrecognized component of the hydrocarbon accumulation history. In particular, it indicates that the region received early petroleum charges that were less mature than currently produced light oil and gas condensates, possibly from the prolific Early Silurian Qusaiba shale source rock and other sources. This has significant implications for prospecting for additional oil, particularly in the north/northwest of the Ghazal region where paleo-oil accumulations may have been displaced or spilled. The lower portion of the Unayzah reservoir (Unayzah-C) remained water-wet during early filling of the upper reservoir unit (Unayzah-A) and appears to have been filled only by a late oil charge. Anomalous molecular and carbon isotopic behavior of residual oil extracts from the uppermost segment of the Unayzah reservoir, where the free oil (first of the sequential extracts) is less mature (0.95% Rc) and isotopically lighter (δ13C?31.15‰) than the adsorbed oil (last sequential extract, 1.05% Rc; δ13C?29.65‰), suggests a late oil contribution or bitumen contamination from the overlying Khuff Formation.  相似文献   

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