Biomarker and n-alkane compound specific stable carbon isotope analyses (CSIA) were carried out on 58 crude oil samples from shallow water and deepwater fields of the Niger Delta in order to predict the depositional environment and organic matter characteristics of their potential source rocks. Using a source organofacies prediction approach from oil geochemistry, the presence in the western deepwater oils relatively abundant C27 steranes, C30 24-n-propyl cholestane, low oleanane index, relatively low pr/ph ratios, gammacerane, and positive to nearly flat C12–C30n-alkane compound specific stable carbon isotope profiles, suggests that the source facies that expelled these oils contain significant marine derived organic matter deposited under sub-oxic and stratified water column conditions. This contrasts with the terrigenous organic matter dominated source rocks accepted for shallow water Niger Delta oils. Oils in the shallow water accumulations can be separated into terrigenous and mixed marine-terrigenous families. The terrigenous family indicates expulsion from source rock(s) containing overwhelmingly higher plant source organic matter (average oleanane index = 0.48, high C29 steranes) as well as having negative sloping n-alkane isotope profiles. Oxic source depositional conditions (pr/ph > 2.5) and non-stratified conditions (absence to low gammacerane content) are inferred for the terrigenous family. The mixed marine-terrigenous family has biomarker properties that are a combination of the deepwater and terrigenous shallow water oils. Bitumen extracts of the sub-delta Late Cretaceous Araromi Formation shale in the Dahomey Basin are comparable both molecularly and isotopically to the studied western deepwater oil set, but with an over all poor geochemical correlation. This poor geochemical match between Araromi shale and the western deepwater oils does not downgrade the potential of sub-delta Cretaceous source rock contribution to the regional oil charge in the deepwater Niger Delta. 相似文献
Up until now, it has been assumed that oil in the Palaeozoic reservoirs of the Tazhong Uplift was derived from Upper Ordovician source rocks. Oils recently produced from the Middle and Lower Cambrian in wells ZS1 and ZS5 provide clues concerning the source rocks of the oils in the Tazhong Uplift, Tarim Basin, China. For this study, molecular composition, bulk and individual n-alkane δ13C and individual alkyl-dibenzothiophene δ34S values were determined for the potential source rocks and for oils from Cambrian and Ordovician reservoirs to determine the sources of the oils and to address whether δ13C and δ34S values can be used effectively for oil–source rock correlation purposes. The ZS1 and ZS5 Cambrian oils, and six other oils from Ordovician reservoirs, were not significantly altered by TSR. The ZS1 oils and most of the other oils, have a “V” shape in the distribution of C27–C29 steranes, bulk and individual n-alkane δ13C values predominantly between −31‰ to −35‰ VPDB, and bulk and individual alkyldibenzothiophene δ34S values between 15‰ to 23‰ VCDT. These characteristics are similar to those for some Cambrian source rocks with kerogen δ13C values between −34.1‰ and −35.3‰ and δ34S values between 10.4‰ and 21.6‰. The oil produced from the Lower Ordovician in well YM2 has similar features to the ZS1 Cambrian oils. These new lines of evidence indicate that most of the oils in the Tazhong Uplift, contrary to previous interpretations, were probably derived from the Cambrian source rocks, and not from the Upper Ordovician. Conversely, the δ13C and δ34S values of ZS1C Cambrian oils have been shown to shift to more positive values due to thermochemical sulfate reduction (TSR). Thus, δ13C and δ34S values can be used as effective tools to demonstrate oil–source rock correlation, but only because there has been little or no TSR in this part of the section. 相似文献
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
Sixty-five natural gas samples were collected from 19 oil-gasfields in the Qaidam basin, China. The chemical composition and carbon isotope values of the samples were measured, and the geochemical characteristics and origin of the natural gases were studied. The gases can be divided into biogenic gases, sapropelic oil-type gases, mixed type oil-type gases, coal-type gases and mixed gas. The δ13Ci values of the biogenic gases are very small and the C2+ contents of them are very low, ranging from -68.2‰ to -61.8‰ and 0.06% to 0.20% respectively. They have heavy δD and δ13Cco2> showing a CC>2 reduction pathway. They are distributed in the East depression region and derived from the Quaternary source rocks. The sapropelic oil-type gases have small δ13C2 values and high C2+ ranging from -36.6‰ to -28.6‰ and from 33.01% to 47.15% respectively. The mixed type oil-type gases have <5I3C2 values and C2+ contents varying from -28.6‰ to -24.8‰ and from 4.81% to 26.06% respectively. Both sapropelic oil-typ 相似文献
Based on the systematic analyses of light hydrocarbon, saturate, aromatic fractions and C isotopes of over 40 oil samples along with related Tertiary source rocks collected from the western Qaidam basin, the geochemical characteristics of the Tertiary saline lacustrine oils in this region was investigated. The oils are characterized by bimodal n-alkane distributions with odd-to-even (C11–C17) and even-to-odd (C18–C28) predominance, low Pr/Ph (mostly lower than 0.6), high concentration of gammacerane, C35 hopane and methylated MTTCs, reflecting the high salinity and anoxic setting typical of a saline lacustrine depositional environment. Mango’s K1 values in the saline oils are highly variable (0.99–1.63), and could be associated with the facies-dependent parameters such as Pr/Ph and gammacerane indexes. Compared with other Tertiary oils, the studied Tertiary saline oils are marked by enhanced C28 sterane abundance (30% or more of C27–C29 homologues), possibly derived from halophilic algae. It is noted that the geochemical parameters of the oils in various oilfields exhibit regular spatial changes, which are consistent with the depositional phase variations of the source rocks. The oils have uncommon heavy C isotopic ratios (−24‰ to −26‰) and a flat shape of the individual n-alkane isotope profile, and show isotopic characteristics similar to marine organic matter. The appearance of oleanane and high 24/(24 + 27)-norcholestane ratios (0.57–0.87) in the saline oils and source rocks confirm a Tertiary organic source. 相似文献
High maturity oil and gas are usually generated after primary oil expulsion from source rocks, especially from oil prone type I/II kerogen. However, the detailed impacts of oil expulsion, or retention in source rock on further thermal degradation of kerogen at the high maturity stage remain unknown. In the present study, we collected an Ordovician Pingliang shale sample containing type II kerogen. The kerogens, which had previously generated and expelled oil and those which had not, were prepared and pyrolyzed in a closed system, to observe oil expulsion or oil retention effects on later oil and gas generation from kerogen. The results show that oil expulsion and retention strongly impacts on further oil and gas generation in terms of both the amount and composition in the high maturity stage. Gas production will be reduced by 50% when the expulsion coefficient reaches 58%, and gas from oil-expelled kerogen (less oil retained) is much drier than that from fresh kerogen. The oil expulsion also causes n-alkanes and gas compounds to have heavier carbon isotopic compositions at high maturity stages. The enrichment of 13C in n-alkanes and gas hydrocarbons are 1‰ and 4–6‰ respectively, compared to fresh kerogen. Oil expulsion may act as open system opposite to the oil retention that influences the data pattern in crossplots of δ13C2–δ13C3 versus C2/C3, δ13C2–δ13C3 versus δ13C1 and δ13C1–δ13C2 versus ln(C1/C2), which are widely used for identification of gas from kerogen cracking or oil cracking. These results suggest that the reserve estimation and gas/source correlation in deep burial basins should consider the proportion of oil retention to oil expulsion the source rocks have experienced. 相似文献
Crude oil has been discovered in the Paleogene and Neogene units of the Weixinan Sag in the Beibu Gulf Basin. To determine the source and accumulation mode of this crude oil, 12 crude oil samples and 27 source rock samples were collected and an extensive organic geochemical analysis was conducted on them. Based on the geological conditions and the analytical results, the types, origins and accumulation patterns of crude oil in the study area were elucidated. Except for a shallowly-buried and biodegraded crude oil deposit in Neogene rocks, the crude oil samples in the study area were normal. All of the crude oils were derived from lacustrine source rocks. According to biomarker compositions, the crude oils could be divided into two families, A and B, distinctions that were reinforced by differences in carbon isotope composition and spatial distribution. Oil-source correlation analysis based on biomarkers revealed that Family A oils were derived from the mature oil shale at the bottom of the second member of the Liushagang Formation, while the Family B oils formed in the mature shale of the Liushagang Formation. The Family A oils, generated by oil shale, mainly migrated laterally along sand bodies and were then redistributed in adjacent reservoirs above and below the oil shale layer, as well as in shallow layers at high structural positions, occupying a wide distribution range. The Family B oils were generated by other shale units before migrating vertically along faults to form reservoirs nearby, resulting in a narrow distribution range. 相似文献
The Upper Triassic Xujiahe Formation in the Sichuan Basin, SW China consists of a series of coal measures. The first, third and fifth members of this formation are dominated by gas prone dark mudstones and coals. The mudstones contain Type II and III kerogens with average organic carbon contents around 1.96%. These source rocks are mature in the central Sichuan and highly mature in the western Sichuan Basin, characterized by gas generation with subordinate amounts of light oil or condensate oils. The source rocks are intercalated with the sandstone dominated second, fourth and sixth members of the Xujiahe Formation, thus leading to three separate self contained petroleum systems in the region. The proven gas reserves in the Xujiahe Formation are only less than that of the Triassic Feixianguan Formation and the Xujiahe Formation has the second largest gas field (Guang’an gas field) in the basin. Gases derived from the Xujiahe Formation coals generally show a normal stable carbon isotopic trend for C1–C4n-alkanes, with the highest δ13C2 values among the nine gas pay zones in the basin (?20.7‰ to ?28.3‰), and δ13C1 values as low as ?43.0‰ in the central Sichuan. Gas accumulations with an oil leg have also been found in the eastern and southern Sichuan where the thickness of the Xujiahe Formation is significantly reduced. Gases in these accumulations tend to show low δ13C2 values (?30.0‰ to ?36.3‰), characteristic of oil prone source rocks. 相似文献
The presence of shale oil in the Cretaceous Hengtongshan Formation in the Tonghua Basin, drilled by the well TD-01, has been discussed in this geological investigation for the first time. To evaluate the high-quality source rocks of Cretaceous continental shale oil, the distribution characteristics and the evolution of the ancient environment, samples of shale were systematically analyzed in terms of sedimentary facies, organic geochemistry, and organic carbon isotopic composition. The results demonstrate that a TOC value of 1.5% represents the lower-limit TOC value of the high-quality source rocks. Source rocks have an aggregate thickness of 211 m and contain abundant organic matter, with TOC values of 2.69% on average and a maximum value over 5.44%. The original hydrocarbon-generative potential value(S_1+S_2) is between 0.18 mg/g and 6.13 mg/g, and the Ro is between 0.97% and 1.40%. The thermal maturation of the source rocks is relatively mature to highly mature. The δ13C value range is between -34.75‰ and -26.53‰. The ratio of saturated hydrocarbons to aromatic hydrocarbons is 1.55 to 5.24, with an average of 2.85, which is greater than 1.6. The organic types are mainly type Ⅱ_1, followed by type Ⅰ. The organic carbon source was C_3 plants and hydrophytes. The paleoclimate of the Hengtongshan Formation can be characterized as hot and dry to humid, and these conditions were conducive to the development of high-quality source rocks. A favorable paleoenvironment and abundant organic carbon sources provide a solid hydrocarbon generation base for the formation and accumulation of oil and gas in the shale of the Tonghua Basin. 相似文献
Through natural gas exploration in the Changling Fault Depression,abundant natural gas flows were obtained and high-quality source rocks were also reveiled.Based on bulk analyses,organic matter abundance,organic matter type and thermal maturity of the source rocks were studied systematically.At the same time,gas gener-ating intensity and gas generating quantity were quantitatively analyzed by using basin modeling technologies.The results indicated that gas source rocks of the Shahezi Formation are characterized by abundant organic matter and dark mudstone distributions and high-over thermal maturity.They possess high gas generating intensity with the biggest value surpassing 500×108 m3/km2,and large gas generating quantity,accounting from 74.40% of the total amount.The Yingcheng Formation has good gas-source rocks with moderate dark mudstone and relatively high organic matter.It has type-Ⅲ organic matter and low-over thermal maturity.The gas generating intensity is moderate,between 20×108 and 60×108 m3/km2.The gas generating quantity is 13.63% of the total amount.The Huoshiling Formation has relatively good source rocks with limited dark mudstone and low organic matter.It has type-Ⅲ kerogen and over-thermal maturity.The gas generating quantity is 7.10% of the total amount.The Denglouku Formation has poor-gas source rocks,and is characterized by undeveloped dark mudstone and low organic matter abundance.It has type-Ⅲ organic matter and low-high thermal maturity.Hydrocarbon gases in the Changling Fault Depression mainly originated from the Shahezi Formation,and secondarily from the Yingcheng Formation.The contribution of the Huoshiling Formation gas source rocks is relatively small. 相似文献
Carbon isotopic compositions were determined by GC–IRMS for individual n-alkanes in crude oils and the free, adsorbed and inclusion oils recovered by sequential extraction from reservoir rocks in the Tazhong Uplift and Tahe oilfield in the Tabei Uplift of Tarim Basin as well as extracts of the Cambrian–Ordovician source rocks in the basin. The variations of the δ13C values of individual n-alkanes among the 15 oils from the Tazhong Uplift and among the 15 oils from the Triassic and Carboniferous sandstone reservoirs and the 21 oils from the Ordovician carbonate reservoirs in the Tahe oilfield demonstrate that these marine oils are derived from two end member source rocks. The major proportion of these marine oils is derived from the type A source rocks with low δ13C values while a minor proportion is derived from the type B source rocks with high δ13C values. Type A source rocks are within either the Cambrian–Lower Ordovician or the Middle–Upper Ordovician strata (not drilled so far) while type B source rocks are within the Cambrian–Lower Ordovician strata, as found in boreholes TD2 and Fang 1. In addition, the three oils from the Cretaceous sandstone reservoirs in the Tahe oilfield with exceptionally high Pr/Ph ratio and δ13C values of individual n-alkanes are derived, or mainly derived, from the Triassic–Jurassic terrigenous source rocks located in Quka Depression.The difference of the δ13C values of individual n-alkanes among the free, adsorbed and inclusion oils in the reservoir rocks and corresponding crude oils reflects source variation during the reservoir filling process. In general, the initial oil charge is derived from the type B source rocks with high δ13C values while the later oil charge is derived from the type A source rocks with low δ13C values.The δ13C values of individual n-alkanes do not simply correlate with the biomarker parameters for the marine oils in the Tazhong Uplift and Tahe oilfield, suggesting that molecular parameters alone are not adequate for reliable oil-source correlation for high maturity oils with complex mixing. 相似文献
The South Oman Salt Basin (SOSB) is host to the world’s oldest known commercial deposits. Most of the South Oman oils have been proven to be associated with the source rocks of the Neoproterozoic to Cambrian Huqf Supergroup, but the assignment of oils to specific Huqf intervals or facies has been hampered by the geochemical similarity of the organic matter across the entire Huqf sequence, possibly as a consequence of limited change in the local palaeoenvironment and biota over the time of its deposition. This study was conducted to establish improved correlations between organic-rich rock units and reservoir fluids in the SOSB through detailed molecular and isotopic analysis of the Huqf Supergroup, with special emphasis directed towards understanding the Ara carbonate stringer play.Unusual biomarkers, tentatively identified as A-norsteranes, show distinctive patterns among carbonate stringer oils and rocks different from those observed in Nafun sediments and Ara rocks from the Athel basin. These putative A-norsteranes form the basis for new oil-source correlations in the SOSB and provide for the first time geochemical evidence of a self-charging mechanism for the carbonate stringer play. The paucity of markers specific to the Nafun Group (Shuram, Buah and Masirah Bay formations) confounds attempts to quantify their respective contributions to Huqf oil accumulations. Nafun inputs can only be determined on the basis of subtle differences between Nafun and Ara biomarker ratios. The most useful geochemical characteristics delineating Nafun Group organic matter from Ara Group intra-salt source rocks included: low relative abundance of mid-chain monomethyl alkanes (X-compounds); low relative abundance of gammacerane, 28,30-dinorhopane, 25,28,30-trinorhopane and 2-methylhopanes; low C22T/C21T and high C23T/C24T cheilanthanes ratio values. Based on these parameters, molecular evidence for major contributions of liquid hydrocarbons from Nafun Group sediments (Shuram, Buah and Masirah Bay formations) is lacking. Our results suggest that the majority of SOSB hydrocarbon accumulations originate from within the Ara group, either from the carbonate stringers or from the package of sediments that comprises the Thuleilat, Athel Silicilyte and U shale formations. Subtle aspects of the composition of some carbonate stringer and post-salt Huqf oils could suggest some degree of sourcing from the Nafun rocks but stronger evidence is needed to confirm this. 相似文献
Stable carbon isotopic composition of organic matter (δ13Corg) and compound-specific δ13C values of biomarkers from 15 lacustrine source rocks were analyzed to identify the original paleoenvironment and source organisms. The δ13C values of hopanes (δ13Chop) ranged from −68.7‰ to −32‰ and exhibit strongly 13C-depleted values in the lower part of Member 1 of the Nenjiang Formation (K2n1, up to −68.7‰), suggesting an origin from predominantly methanotrophic bacteria. 13C-enriched δ13CGa values and significantly 13C-depleted δ13Chop in K2n1, which coincide with water stratification and an intermittent anoxic photic zone, represents a shallow chemocline. The presence of an intermittent anoxic photic zone, which means that the anoxia expanded into the euphotic zone, is beneficial for OM preservation and results in high values of TOC and HI in this section. However, the absence of gammacerane and 13C-enrichment of δ13Chop in Member 2 of Nenjiang Formation (K2n2) reflect a deeper chemocline, corresponding to relatively oxidizing conditions and low values of TOC and HI. Moreover, the negative correlation of TOC vs δ13Corg and HI vs δ13Corg reflects the control of OM formation by sedimentary environments rather than productivity in the water column. Thus, the depth of the chemocline not only controls the abundance of OM but also affects the development of the microbial community, such as chemoautotrophic bacteria in the deep chemocline and chemoautotrophic and methanotrophic bacteria in the shallow chemocline. Moreover, δ13CGa and δ13C values for 4-methyl steranes are related to water salinity, with a higher salinity accompanied by 13C-enrichment in gammacerane and 4-methyl steranes. 相似文献
The free, adsorbed and inclusion oils were recovered by sequential extraction from eleven oil and tar containing reservoir rocks in the Tazhong Uplift of Tarim Basin. The results of gas chromatography (GC) and GC–mass spectrometry analyses of these oil components and seven crude oils collected from this region reveal multiple oil charges derived from different source rocks for these oil reservoirs. The initially charged oils show strong predominance of even over odd n-alkanes in the range n-C12 to n-C20 and have ordinary maturities, while the later charged oils do not exhibit any predominance of n-alkanes and have high maturities. The adsorbed and inclusion oils of the reservoir rocks generally have high relative concentrations of gammacerane and C28 steranes, similar to the Cambrian-Lower Ordovician source rocks. In contrast, the free oils of these reservoir rocks generally have low relative concentrations of gammacerane and C28 steranes, similar to the Middle-Upper Ordovician source rocks. There are two interpretations of this result: (1) the initially charged oils are derived from the Cambrian-Lower Ordovician source rocks while the later charged oils are derived from the Middle-Upper Ordovician source rocks; and (2) both the initially and later charged oils are mainly derived from the Cambrian-Lower Ordovician source rocks but the later charged oils are contaminated by the oil components from the Silurian tar sandstones and the Middle-Upper Ordovician source rocks. 相似文献
Subaerial exposure and oxidation of organic carbon (Corg)-rich rocks is believed to be a key mechanism for the recycling of buried C and S back to Earth's surface. Importantly, processes coupled to microbial Corg oxidation are expected to shift new biomass δ13Corg composition towards more negative values relative to source. However, there is scarcity of information directly relating rock chemistry to oxidative weathering and shifting δ13Corg at the rock-atmosphere interface. This is particularly pertinent to the sulfidic, Corg-rich alum shale units of the Baltoscandian Basin believed to constitute a strong source of metal contaminants to the natural environment, following subaerial exposure and weathering. Consistent with independent support, we show that atmospheric oxidation of the sulfidic, Corg-rich alum shale sequence of the Cambrian-Devonian Baltoscandian Basin induces intense acid rock drainage at the expense of progressive oxidation of Fe sulfides. Sulfide oxidation takes priority over microbial organic matter decomposition, enabling quantitative massive erosion of Corg without producing a δ13C shift between acid rock drainage precipitates and shale. Moreover, 13C enrichment in inorganic carbon of precipitates does not support microbial Corg oxidation as the predominant mechanism of rock weathering upon exposure. Instead, a Δ34S = δ34Sshale − δ34Sprecipitates ≈ 0, accompanied by elevated S levels and the ubiquitous deposition of acid rock drainage sulfate minerals in deposited efflorescent precipitates relative to shales, provide strong evidence for quantitative mass oxidation of shale sulfide minerals as the source of acidity for chemical weathering. Slight δ15N depletion in the new surface precipitates relative to shale, coincides with dramatic loss of N from shales. Collectively, the results point to pyrite oxidation as a major driver of alum black shale weathering at the rock-atmosphere interface, indicating that quantitative mass release of Corg, N, S, and key metals to the environment is a response to intense sulfide oxidation. Consequently, large-scale acidic weathering of the sulfide-rich alum shale units is suggested to influence the fate and redistribution of the isotopes of C, N, and S from shale to the immediate environment. 相似文献
A large amount of deep oil has been discovered in the Tazhong Uplift, Tarim Basin whereas the oil source is still controversial. An integrated geochemical approach was utilized to unravel the characteristics, origin and alteration of the deep oils. This study showed that the Lower Cambrian oil from well ZS1C (1x) was featured by small or trace amounts of biomarkers, unusually high concentration of dibenzothiophenes (DBTs), high δ34S of DBTs and high δ13C value of n-alkanes. These suggest a close genetic relationship with the Cambrian source rocks and TSR alteration. On the contrary, the Middle Cambrian oils from well ZS1 (2a) were characterized by low δ13C of n-alkanes and relatively high δ34S of individual sulfur compounds and a general “V” shape of steranes, indicating a good genetic affinity with the Middle–Upper Ordovician source rocks. The middle Cambrian salt rock separating the oils was suggested to be one of the factors responsible for the differentiation. It was suggested that most of the deep oils in the Tazhong Uplift were mixed source based on biomarkers and carbon isotope, which contain TSR altered oil in varied degree. The percentage of the oils contributed by the Cambrian–Lower Ordovician was in the range of 19–100% (average 57%) controlled by several geological and geochemical events. Significant variations in the δ34S values for individual compounds in the oils were observed suggesting a combination of different extent of TSR and thermal maturation alterations. The unusually high DBTs concentrations in the Tazhong-4 oilfield suggested as a result of mixing with the ZS1C oil (1x) and Lower Ordovician oils based on δ34S values of DBT. This study will enhance our understanding of both deep and shallow oil sources in the Tazhong Uplift and clarify the formation mechanisms of the unusually high DBTs oils in the region. 相似文献
