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1.
Based on quantitative GC-MS analysis of 40 crude oil samples collected from the south area of western Qaidam Basin,one of the largest saline lacustrine basins in China,the geochemical characteristics of aromatic hydrocarbons in oils were studied systematically in this paper.Among those constitutes,naphthalene(43% 59%),phenanthrene(12% 21%) and taromatic-sterane series(6% 28%) were the main ones of aromatic hydrocarbons.The ratio of aromatic hydrocarbon maturity parameter vs.saturated hydrocarbon maturity parameter C 29 20S/(20S+20R) shows that some aromatic hydrocarbon maturity parameters are not suitable for low-mature oils,including MPI,MNR,DNR,etc.Meanwhile,maturity parameters for dibenzothiophene and taromatic-sterane series are more appropriate for low maturity saline lacustrine crude oils.Based on the ratio of 4,6-DMDBT/1,4-DMDBT,the R c values are within the range of 0.59% 0.72%.However,the abundance of dibenzothiophene(DBT) is low,and the dibenzofuran(DBF) content is even lower,suggesting that the crude oils were formed in a saline lacustrine anaerobic environment.The high abundance of C 26 triaromatic steroid also indicates that the source material is brackish water-saline water with strong reducibility.  相似文献   

2.
Bicyclanes previously reported only in heavily biodegraded Texas Gulf Coast crudes have been found to be ubiquitous in Australian crude oils of non-marine origin from four different basins. The compounds are present in oils, thought to be derived from the same or similar sources, that have undergone varying degrees of biodegradation. They are also found to be present in oils of different geological age. In addition a series of tricyclic diterpenoid hydrocarbons was common to four oils from the Gippsland Basin. Four of these compounds had the molecular formula C20H34 and mass spectral fragmentation patterns suggested they were mono-unsaturated diterpenoids. The presence of unsaturated diterpenoids in crude oils appears to be a unique observation. It is proposed that the diterpenoids may be the source of the bicyclanes also observed in these oils.  相似文献   

3.
The present paper deals with the biomarker characteristics of crude oils and source rocks from different environments(fresh,fresh-brackish and salt waters)of nonmarine depositional basins of different ages in China.Their characters are summarized as follows:1)Souce rocks and crude oils derived from fresh-water lacustrine facies have an odd/even predominance of n-alkanes and high pristine/phytane ratios.Oils from the fresh-water lacustrine facies differ from typical marine oils in the relative contents of total steranes and terpanes,the concentrations of hopanes and organic sul-phur compounds and the values of methylphenanthrene indices and C,H,S stable isotopes.2)The source rocks and crude oils derived from saline lacustrine facies possess an even/odd predominance of n-alkanes and high phytane/pristine ratios.There are also some differences between saline lacustrine oils and freshwater lacustrine oils in the concentrations of steranes,tricyclic terpanes and organic sulphur compounds,as well as in the values of methylphenanthrene indices and C,H,S stable isotopes.3)Oils derived from fresh-brackish water lake facies differ from oils from fresh-water lacustrine or samline lacustrine environments in respect of some biomarkers.According to the various distributions of these biomarkers,a number of geochemical parameters can be applied synthetically to differentiating and identifying the nature of original depositional environments of crude oils and source rocks and that of organisms-primary source materials present in those environments.  相似文献   

4.
High-temperature gas chromatography (HTGC) has enhanced our ability to characterize hydrocarbons extending to C120 in crude oils. As a result, hydrocarbons in waxes (> C20) have been observed to vary significantly between crude oils, even those presumed to originate from the same source. Prior to this development, microcrystalline waxes containing hydrocarbons above C40 were not characterized on a molecular level due to the analytical limitations of conventional gas chromatography. Routine screenings of high pour-point crude oils by high-temperature gas chromatography has revealed that high molecular weight hydrocarbons (> C40) are very common in most oils and may represent 2% of the crude oil. Precise structures, origins, and significance of these high molecular weight compounds remain elusive. As a preliminary step to expand our knowledge of these compounds their general molecular structures and formulas have been investigated in this study. Initial results suggest that the major high molecular weight compounds include a homologous series of n-alkanes, methylbranched alkanes, alkylcyclopentanes, alkylcyclohexanes, alkylbenzenes and alkylcycloalkanes.  相似文献   

5.
The physical properties and group compositions of crude oils in the western depression of the Liaohe Basin possess such characteristics as to increase gradually in density, viscosity and wax contents, and decrease in saturated hydrocarbon and non-hydrocarbon and bitumen contents from the deep level to the shallow level and from the center of the depression to its boundary. Saturated hydrocarbons have various spectra, such as single peak and double peak patterns, front peak and rear peak patterns, and smooth peak and serated peak patterns, as well as the chromatograms of biodegraded n-alkanes. The ratios of Pr/Ph in crude oils from the southern part of the depression are generally higher than those in the northern part. The distribution of regular steranes C27–C29 is predominantly of the ramp type, and only a few samples have relatively high C28 contents in the southern part of the depression. As viewed from their physical properties and geochemical characteristics, crude oils in the study area can be divided into two types (I and II) based on oil-generating sources and sedimentary environments, and then further divided into three sub-types (Ia, Ib and Ic:IIa, IIb and IIIc, respectively) based on their degrees of maturation and secondary transformation. This will provide the reliable basis for oil-source correlation and petroleum exploration and prediction.  相似文献   

6.
In a previous study, oils in the Potwar Basin (Upper Indus) of Pakistan were correlated based on the dissimilarity of source and depositional environment of organic matter (OM) using biomarkers and bulk stable isotopes. This study is aimed at supporting the classification of Potwar Basin oils into three groups (A, B and C) using the distribution of alkylnaphthalenes, alkylphenanthrenes, alkyldibenzothiophenes, alkyldibenzofurans, alkylfluorenes, alkylbiphenyls, triaromatic steroids, methyl triaromatic steroids, retene, methyl retenes and cadalene. The higher relative abundance of specific methyl isomers of naphthalene and phenanthrene and the presence of diagnostic aromatic biomarkers clearly indicate the terrigenous and oxic depositional environment of OM for group A oil. Group B and C oils are of marine origin and the aforementioned heterocyclic and polycyclic aromatic hydrocarbons (HCs) differentiate them clearly into two different groups. The relative percentages of heterocyclic aromatic HCs reveal that the distribution of these compounds is controlled by the depositional environment of the OM. Sulfur-containing heterocyclic aromatic HCs are higher in crude oils generated from source rocks deposited in suboxic depositional environments, while oxygen-containing heterocyclic aromatic HCs in combination with alkylfluorenes are higher in marine oxic and deltaic oils. Biomarker and aromatic HC parameters do not indicate significant differences in the thermal maturity of Potwar Basin oils. Triaromatic and methyl triaromatic steroids support the division of Potwar Basin oils into the three groups and their relative abundances are related to source OM rather than thermal maturity. Significantly higher amounts of C20 and C21 triaromtic steroids and the presence or absence of long chain triaromatic steroids (C25, C26, C27, and C28) indicates that these compounds are probably formed from different biological precursors in each group. Different isomers of methyl substituted triaromatic steroids are present only for short chain compounds (C20–C22) and the origin of these compounds may be short chain methyl steranes from unknown biological precursors.  相似文献   

7.
塔里木盆地原油噻吩类化合物的组成特征及地球化学意义   总被引：9，自引：1，他引：8  
张敏  张俊 《沉积学报》1999,17(1):120-126
对塔里木盆地典型原油噻吩类化合物含量和组成特征研究,发现不同类型原油苯并萘噻吩和二苯并噻吩系列化合物占芳烃化合物的百分含量相差明显,海相油含量最高,湖相油次之,而煤成油最低。本文提出了４－甲基二苯并噻吩／二苯并噻吩、（２＋３）－甲基二苯并噻吩／二苯并噻吩比值是区分海相油和湖相油新的有机地球化学参数。二苯并噻吩系列化合物最大烷化度表明海相油呈现出高烷化度,而陆相油则表现为低烷化度,即从海相泥灰岩原油、海相碳酸盐岩原油到湖相油和煤成油依次减少。这是因为富硫与贫硫干酪根在生烃过程中的环化作用或支链化作用程度差异所造成的。  相似文献   

8.
Steroids with unconventional side chains have increasingly been applied as diagnostic markers for geological source and age assessments. However, one of the most distinctive characteristics, the abnormal abundance of pregnane and homopregnane in ancient sediments and petroleum, remains unresolved. Higher pregnane and homopregnane, as well as C23–C26 20-n-alkylpregnanes, relative to the regular steranes were observed in samples collected from different petroleum basins in China. These included Precambrian marine carbonate-derived petroleum (NW Sichuan Basin), Lower Paleozoic marine marl derived crude oils (Tarim Basin), and Eocene hypersaline lacustrine carbonate source rocks and associated petroleum (Bohai Bay Basin). However, all of the samples have many common biomarker characteristics, such as pristane/phytane ratios < 1, low amounts of diasteranes and high C29/C30 hopane (∼0.6–1), C35/C34 hopane (mostly ⩾ 1) and dibenzothiophene/phenanthrene (DBT/PHEN, mostly 0.5–1) ratios revealing a contribution from anoxic carbonate/marl source rocks deposited in restricted, clastic-starved settings. We suggest that 5α,l4β,l7β-pregnane and homopregnane, as well as their higher C23–C26 homologues, are geological products derived from steroids bound to the kerogen by a sulfurized side chain. Carbon or carbonate minerals are considered to be natural catalysts for this cracking reaction via preferential cleavage of the bond between C-20 and C-22. Similar distributions occur in the short chain analogues of 4-methylsterane, triaromatic steroid and methyltriaromatic steroid hydrocarbons, providing circumstantial evidence for this proposal. The ratio of pregnane and homopregnane to the total regular steranes and the ratio of C27 diasteranes to cholestanes can be sensitive indicators of sedimentary environments and facies. In general, high diasteranes and low pregnanes (with homologues) indicate an oxic water column or significant input of terrigenous organic matter in clay rich source rocks and some organic lean carbonate rocks. Low diasteranes with high pregnanes implies restricted, sulfur rich conditions, typical of anoxic carbonate source rocks. Furthermore, the two ratios may be useful to assess the variation of mineralogy and openness of source rock depositional settings.  相似文献   

9.
Three sulphur-rich commercial crude oils have been studied, which contain sulphur as high as up to 4–12%. These samples were collected from Tertiary hypersaline lake sediments of the Jianghan Basin, Hubei Province at different depths, but above the oil generation threshold (2200m). FPD-GC and GC-MS data show that aromatic fractions of the crude oils are composed of different homologues of sulphur-containing compounds, including long-chain normal alkyl-thiophenes and-thiolanes, long-chain isoprenoid-thiophenes and -thiolanes, and benzothiophenes. It is worth noting that the distribution patterns of long-chain alkyl-thiophenes and -thiolanes from two shallow-seated crude oils are quite similar to those of normal alkanes showing marked even-odd predominance. It seems that the even-odd predominance of sulphur-containing compounds decreases with increasing burial depth of the crude oils. The major component of aliphatic fraction is phytane, and similarly the major peaks of aromatic fractions also represent C20 isoprenoid thiophenes. Some preliminary conclusions have been drawn from the above discussion: (1) Abundant sulphur-containing compounds may be used as an indicator of low mature or immature crude oils produced from hypersaline lake sediments; (2) Sulphur-containing compounds are considered to be early diagenetic products of reactions between elemental sulphur or sulfides and alkanes or their precursors (phytols, fatty acids, alcohols, etc.), or of bacterial activities, but not direct inputs of organisms.  相似文献   

10.
    
The Jiyang Sag and the Liaohe Basin are the two important areas where immature oil resources are distributed in China. From these two areas immature-low mature to mature oil samples were collected for carbon isotopic analysis. The extracts of source rocks are dominant in the Jiyang Sag while crude oils are dominant in the Liaohe Basin. The maturity index, Ro, for source rocks varies from 0.25% (immature) to 0.65% (mature). Studies have shown that within this range of Ro values the extracts of source rocks and crude oils, as well as their fraction components, have experienced observable carbon isotope fractionation. The carbon isotopic values tend to increase with burial depth, the oils become from immature-low mature to mature, and the rules of evolution of oils show a three-stage evolution pattern, i. e., light→heavy→light→heavy oils. Such variation trend seems to be related to the occurrence of two hydrocarbon-generating processes and the main hydrocarbon-forming materials being correspondingly non-hydrocarbons and possessing MAB characteristics, lower thermodynamic effects and other factors. In the process towards the mature stage, with increasing thermodynamic effects, the thermal degradation of kerogens into oil has become the leading factor, and correspondingly the bond-breaking ratio of12C-13C also increases, making the relatively12C-rich materials at the low mature stage evolve again towards13C enrichment. This research project was granted by both the 960006 Project of China Petroleum and Natural Gas Co. and the National Natural Science Foundation of China (Grant No. 49973010).  相似文献   

11.
通过色谱-质谱分析,对海拉尔盆地贝尔凹陷35个原油样品进行聚类分析,将之分成4类.Ⅰ类原油是贝尔凹陷原油主体,占分析样品的77%,特点足菲系列含量高,平均值为64.7%,三芳甾类化合物和三芴类化合物含量次之,分别为11.42%和11.81%.Ⅱ类原油为高三芳甾类原油,三芳甾类化合物占芳烃化合物的53.9%,是该类原油的主要成份,非系列化合物含量较低,为32.5%,萘系列含量和三芴化合物含量最低,分别为0.6%和3.54%.Ⅲ类原油为高菲系列和高萤蒽含量原油,菲系列为64%,萤蒽含量高达11%,是其它原油的16倍以上.Ⅳ类原油具有高萘、高三芴化合物和低菲系列化合物的特点,分别占原油芳烃馏分的30%、32%和26%,三芳甾类化合物含量低,占3.6%.这充分说明海拉尔箍地烃源岩沉积期间有不同的沉积环境,原油有不同的牛烃母质.Ⅱ类原油以藻类为主要生烃母质,Ⅲ类原油以高等植物为主,Ⅰ类原油介于Ⅱ类和Ⅲ类原油之间,为混合型生烃母质.Ⅳ原油沉积环境和前三类原油明显不同,为咸水强还原湖相沉积环境.  相似文献   

12.
Paraffinic crude oils are designated ‘primary’ because their composition is very close or identical to that of the hydrocarbons extracted from the corresponding oil source rocks. Heavy and medium-gravity naphthenic crude oils, on the other hand, typically are quite different compositionally from hydrocarbon mixtures in either mature or immature shales.The normal paraffin carbon number odd/even ratio 2C29/(C28 + C30) of all the heavy to medium-gravity crude oils which could be analysed are in exactly the same range as is observed for the primary paraffinic crude oils, namely 0.95–1.42. The naphthene indices of the medium to heavy gravity naphthenic crude oils and of the primary paraffinic crude oils from the same area are identical or close. These facts are significant because both the n-paraffin carbon number odd/even ratio and the naphthene index of shale hydrocarbons are strongly depth and subsurface temperature dependent. The facts observed demonstrate beyond question that, in the same area, the paraffinic precursors of the heavy to medium-gravity naphthenic crude oils are generated and expelled in the identical depth range, and from the same mature relatively deep oil source beds as the primary paraffinic crude oils. Later, during and/or after a generally upward migration into oil reservoirs, the primary crude may be transformed compositionally into a naphthenic crude oil.In none of the five widely scattered oil basins studied are medium to heavy naphthenic crude oils found at temperatures greater than a limiting subsurface temperature. The abruptness of the temperature cutoff of the change in oil compositions in all five oil basins, as well as the average value of the cutoff temperature of 66°C (150°F), leaves no doubt that the mechanism of this crude oil transformation process is microbial.Optical activity, which was observed in narrow saturate hydrocarbon fractions of the 80–325°C range of all microbially transformed crude oils, but not in the primary untransformed oils, is strong additional evidence for the microbial nature of the crude oil transformation process. The observed optical activity is explained by the microbial digestion at different rates of optical antipodes present in the primary paraffinic crude oils.To gain perspective the vast scale of the microbial oil transformation process in nature is pointed out. Billions of tons of heavy to medium-gravity naphthenic crude oils, originating from the microbial transformation of primary paraffinic oils, are present in oil fields and tar sands all over the world.  相似文献   

13.
Azanaphthalene derivatives were identified in 9 petroleum samples. In all investigated crude oils; the number of alkyl substituents was found to extend up to C9 with a maximum most often for C6; unsubstituted parent compounds are absent. Two distinct types of azanaphthalenes occur: solely methylated derivatives which are abundant in most crude oils of Cretaceous or Miocene ages, and compounds bearing alkyl chains of up to 4 carbon atoms, with a majority of 8-isopropyl quinoline derivatives, which dominate in a California crude oil of Pliocene age.  相似文献   

14.
Geochemical characterisation of 18 crude oils from the Potwar Basin (Upper Indus), Pakistan is carried out in this study. Their relative thermal maturities, environment of deposition, source of organic matter (OM) and the extent of biodegradation based on the hydrocarbon (HC) distributions are investigated. A detailed oil-oil correlation of the area is established. Gas chromatography-mass spectrometry (GC-MS) analyses and bulk stable carbon and hydrogen isotopic compositions of saturated and aromatic HC fractions reveals three compositional groups of oils. Most of the oils from the basin are typically generated from shallow marine source rocks. However, group A contains terrigenous OM deposited under highly oxic/fluvio-deltaic conditions reflected by high pristane/phytane (Pr/Ph), C30 diahopane/C29Ts, diahopane/hopane and diasterane/sterane ratios and low dibenzothiophene (DBT)/phenanthrene (P) ratios. The abundance of C19-tricyclic and C24-tetracyclic terpanes are consistent with a predominant terrigenous OM source for group A. Saturated HC biomarker parameters from the rest of the oils show a predominant marine origin, however groups B and C are clearly separated by bulk δ13C and δD and the distributions of the saturated HC fractions supporting variations in source and environment of deposition of their respective source rocks. Moreover, various saturated HC biomarker ratios such as steranes/hopanes, diasteranes/steranes, C23-tricyclic/C30 hopane, C28-tricyclic/C30 hopane, total tricyclic terpanes/hopanes and C31(R + S)/C30 hopane show that two different groups are present. These biomarker ratios show that group B oils are generated from clastic-rich source rocks deposited under more suboxic depositional environments compared to group C oils. Group C oils show a relatively higher input of algal mixed with terrigenous OM, supported by the abundance of extended tricyclic terpanes (up to C41+) and steranes.Biomarker thermal maturity parameters mostly reached to their equilibrium values indicating that the source rocks for Potwar Basin oils must have reached the early to peak oil generation window, while aromatic HC parameters suggest up to late oil window thermal maturity. The extent of biodegradation of the Potwar Basin oils is determined using various saturated HC parameters and variations in bulk properties such as API gravity. Groups A and C oils are not biodegraded and show mature HC profiles, while some of the oils from group B show minor levels of biodegradation consistent with high Pr/n-C17, Ph/n-C18 and low API gravities.  相似文献   

15.
This study deals with a detailed geochemical characterization of three crude oils from the Upper Indus Basin, Punjab, Pakistan. The samples were obtained from three productive oil fields of the Datta Formation (Jurassic), Lochhart (Palaeocene) and the Dhak Pass zone (Palaeocene). The GC parameters for and the bulk properties of Datta Formation oils are essentially coincident with those of the oils from the Dhak Pass Formation in the Upper Indus Basin, Pakistan and the oils likely originate from a marine source rock. In contrast, the Lockhart Formation oils show different behaviors and seem to be originated from dirty carbonate rocks although all three crude oils are mature, being of non-biodegraded and somewhat mixed organic matter origin. Low Pr/Ph values and high C35 homohopane index for the Lockhart Formation oils suggest a source of anoxic environment with low Eh while oils from the Datta Formation and Dhak Pass Formation showed different trends, i.e., lower values of C35 homohopane index indicating different depositional environment than oil from the Lockhart Formation. All three crude oils from the Upper Indus Basin are mature for the hopane ratios, i.e., Ts/Ts+Tm, C3222S/(S+R) and C30 αβ/(αβ+βα) and sterane ratios, i.e., C2922S/(S+R) and C29ββ/(ββ+αα) but oils from the Lockhart Formation seem to be less mature than those from the Palaeocene and Datta Formation according to plots like API° vs. homohopane Index, Pr/Ph vs. sterane. The relative composition of 5α(H), 14β(H), 17β(H)-24-ethylecholestanes and the C2920S/20S+20R index, indicate that all three crude oils are equally mature, which makes it unlikely with respect to the above said plots. This difference is may be due to the migratory chromatography which alters the concentrations of sterane and hoapnes and hence gives different results. These oils do not exhibit UCM and have complete n-alkane profiles indicating non-biodegradation.  相似文献   

16.
Analyses of some Australian crude oils show that many contain varying concentrations of A/ B-ring demethylated hopanes. These range from C26 to C34 and have been identified from their retention times and mass spectral data as 17α(H)-25-norhopanes. Comparison of hopane and demethylated hopane concentrations and distributions in source-related, biodegraded oils suggests that demethylated hopanes are biotransformation products of the hopanes. Further, it appears that the process occurs at a late stage of biodegradation, after partial degradation of steranes has occurred. Demethylated hopanes are proposed as biomarkers for this stage of severe biodegradation. The presence of these compounds in apparently undegraded crude oils is thought to be due to the presence of biodegraded crude oil residues which have been dissolved by the undegraded crude oil during accumulation in the reservoir sands. The timing of hopane demethylation, relative to the degradation of other compounds, has been assessed and the progressive changes in crude oil composition with increasing extent of biodegradation have been identified. The use of demethylated hopanes as maturity parameters for severely biodegraded crude oils, and the applicability of established biomarker maturity parameters to such oils, are also discussed.  相似文献   

17.
Research on the molecular fossil characteristics of heavy oil from Well Tadong-2 is of great importance to constrain the source of marine crude oils in the Tarim Basin, Xinjiang, China. The authors synthetically applied the isotope mass spectrograph, chromatography and chromatography-mass spectrography to the studies of molecular fossil characteristics of heavy oil from Well Tadong-2 in the Tarim Basin, and the results obtained revealed that heavy oil from Well Tadong-2 is characterized by high gammacerane, high C28 sterane, low rearranged sterane and high C27-triaromatic steroid, these characteristics are similar to those of Cambrian-Lower Ordovician source rocks, demonstrating that Cambrian crude oils came from Cambrian-Lower Ordovician source rocks; condensed compounds (fluoranthene, pyrene, benzo[a]anthracene, bow, benzo fluoranthene, benzopyrene) of high abundance were detected in heavy oil from Well Tadong-2, and the carbon isotopic values of whole oil are evidently heavy, all the above characteristics revealed that hydrocarbons in the crude oils became densified in response to thermal alteration.  相似文献   

18.
Fractionated carbazoles have been detected for the first time in crude oils from the Tazhong area of the Tarim Basin, and these nitrogen compounds were successfully utilized in the study of petroleum migration. Alkylcarbazoles are quite abundant in all the samples analyzed; small amounts of benzocarbazoles were detected only in some of the sample, and dibenzocarbazoles were not found in the oils. Based on the distributions of G1, G2 and G3 types of C2-alkylcarbazoles, the ratio of C3-/C2-carbazoles and the relative concentrations of alkylcarbazole and alkylbenzocarbazole, oils in the Carboniferous CIII reservoir in the Tazhong uplift are thought to have laterally migrated to the high level of Tazhong structure No. 4 from both northwest and southeast. The study here also shows that oils in the area may have undergone long-distance migration. This project is financially supported by the China National Petroleum Corporation and the State Educational Commission.  相似文献   

19.
Organic matter from the Lower Paleozoic strata on the northern margin of the Tarim Basin of China contains abundant alkylcyclohexanes.The n-alkylcyclohexanes show the even(C16-C20) and odd (C17-C21) carbon number predominance and smooth distribution,and the methyl-n-alkylcycolhexanes the odd carbon number predominance(C17-C21) and smooth distribution,which may be related to their depositional environments and organic precursors.There are some differences in carbon number distribution between the two series of monocyclic alkanes and the n-alkanes marked by smooth distribution.The genetic relationship between the three series of compounds needs to be further studied.  相似文献   

20.
A suite of 27 oils from the Qinjiatun–Qikeshu oilfields in the Lishu Fault Depression of the Songliao Basin was analyzed using whole oil gas chromatography. In combination with the relative distribution of C27, C28, and C29 regular steranes, detailed geochemical analyses of light hydrocarbons in oil samples revealed crude oils characterized by the dual input of lower aquatic organisms and higher terrestrial plants. Several light hydrocarbon indicators suggest that the liquid hydrocarbons have maturities equivalent to vitrinite reflectances of around 0.78%–0.93%. This is consistent with the maturity determination of steranes C29 20S/(20S + 20R) and C29 ααβ/(ααα + αββ). Crude oils derived from the two distinct oilfields likely both have source rocks deposited in a lacustrine environment based on light hydrocarbon parameters and on higher molecular weight hydrocarbon parameters. The results show that light hydrocarbon data in crude oils can provide important information for understanding the geochemical characteristics of the Qinjiatun–Qikeshu oils during geologic evolution.  相似文献   

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