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1.
Coal beds of the Upper Cretaceous Fruitland Formation in the San Juan Basin of northwestern New Mexico and southwestern Colorado have significant liquid hydrocarbon generation potential as indicated by typical Rock-Eval Hydrogen Indexes in the range of 200–400 mg hydrocarbon/g organic carbon (type II and III organic matter). Small, non-commercial quantities of oil have been produced from the coal beds at several locations. The oils are characterized by high pristane/phytane (ca 4) and pristane/n-C17 ratios (ca 1.2), abundant C21+ alkanes in the C10+ fraction with a slight predominance of odd carbon-numbered n-alkanes, abundant branched-chain alkanes in the C15+ region, and a predominance of methylcyclohexane in the C4----C10 fraction. The oils are indigenous to the Fruitland Formation coals and probably migrated at thermal maturities corresponding to vitrinite reflectance values in the range 0.7–0.8%. Although the oils found to date are not present in commercial amounts, these findings illustrate the potential of some coals to generate and expel oil under conditions of moderate thermal heating.  相似文献   

2.
A detailed organic geochemical study; utilising petrography, biomarker hydrocarbon analysis and high temperature GC analysis of extractable wax hydrocarbon constituents was performed on four marginally oil window-mature source rocks from the Shahejie Formation (Eocene), Damintun depression in eastern China. The main maceral components in the source rocks were vitrinite, liptinite and exinite, with vitrinite being more abundant (>50 vol.%) in organic-lean samples whose TOC contents were between 1 and 2 wt.%. Large differences in pristane/phytane ratios suggested that the organic-rich samples were deposited in a less oxic depositional environment than that for the organic-lean rocks. The distribution of extractable wax hydrocarbons, determined by high temperature GC, showed a marked difference between these two sample types. The organic-rich samples contained high molecular weight hydrocarbons (HMWHCs) dominated by macrocrystalline n-alkanes (n-C23–n-C37, typically maximising at n-C29), while the organic-lean samples contained lower amounts of extractable wax hydrocarbons but were relatively rich in microcrystalline components (> n-C35). In all source rocks (Es3 and Es4), a noticeable odd-over-even predominance (OEP) of n-alkane chain lengths (up to n-C65) was evident, consistent with a direct biological origin for the long n-alkyl chains. They were most probably formed during diagenesis from decarboxylation of predominantly even-carbon-numbered aliphatic acids originating from higher plant or lacustrine algal sources and/or were directly biosynthesised in hydrocarbon form. At least two other homologous series of branched/cyclic HMWHCs were observed, one of which was confirmed as a series of branched alkanes (probably methyl-branched). The carbon number distribution patterns of HMWHCs may be primarily controlled by thermal maturity and biogenic source input as well as being influenced by diagenetic reactions governed by depositional environmental conditions, as shown previously [Carlson, R.M.K., Teerman, S.C., Moldowan, J.M., Jacobson, S.R., Chan, E.I., Dorrough, K.S., Seetoo, W.C., Mertani, B., 1993. High temperature gas chromatography of high wax oils. In: Indonesian Petroleum Association, 22nd Annual Convention Proceedings. Jakarta, Indonesian, pp. 483–507. Carlson, R.M.K., Jacobsen, S.R., Moldowan, J.M., Chan E.I., 1994. Potential application of high temperature gas chromatography to Middle Eastern petroleum exploration and production. In: Al-Husseini, M.I. (Ed.), Geo'94, Vol 1., Selected Middle East Papers from The Middle East Petroleum Geoscience Conference, 1994; Gulf PetroLink. Manama, Bahrain, pp. 258–267]. Our study indicates for the first time that Es3 source rocks as well as Es4 facies contain HMWHCs. The distributions of extractable wax hydrocarbons suggest that both Es4 and Es3 members may potentially serve as important parent source rocks for generating waxy petroleum in this region.  相似文献   

3.
The upper part of Madbi Formation organic-rich shale is considered an important regional source rock in the Masila Basin, Yemen. Ten cutting samples from this Upper Jurassic organic-rich shale were collected from wells drilled in the Kharir Oilfield, Masila Basin in order to geochemically assess the type of organic matter, thermal maturity and depositional environment conditions. Results reveal that Upper Jurassic organic-rich shale samples contain high organic matter more than 2.0 wt.% TOC and have very good to excellent hydrocarbon potential. Marine algae organic matter is the main source input for the Upper Jurassic shale sequence studied. This has been identified from organic petrographic characteristics and from the n-alkane distributions, which dominated by n-C14-n-C20 alkanes. This is supported by the high value of the biomarker sterane/hopane ratio that approaches unity, as well as the relatively high C27 sterane concentrations. A mainly suboxic depositional environment is inferred from pr/ph ratios (1.75–2.38). This is further supported by relatively high homohopane value, which is dominated by low carbon numbers and decrease towards the C35 homohopane. The concentrations of C35 homohopane are very low. The depositional environment conditions are confirmed by some petrographic characteristics (e.g. palynofacies). Detailed palynofacies analysis of Madbi shales shows that the Madbi shale formation is characterised by a mix of amorphous organic matter, dinoflagellates cysts and phytoclasts, representing a suboxic, open marine setting. The Upper Jurassic marine shale sequence in the Masila Basin is thermally mature for hydrocarbon generation as indicated by biomarker thermal maturity parameters. The 22 S/22 S + 22R C32 homohopane has reached equilibrium, with values range from 0.58 to 0.62 which suggest that the Upper Jurassic shales are thermally mature and that the oil window has been reached. 20 S/(20 S + 20R) and ββ/(ββ + αα) C29 sterane ratios suggest a similar interpretation, as do the moretane/hopane ratio. This is supported by vitrinite reflectance data ranging from 0.74% to 0.90%Ro and thermal alteration of pollen and spore. The thermal alteration index value is around 2.6–3.0, corresponding to a palaeotemperature range of 60–120°C. These are the optimum oil-generating strata. On the basis of this study, the Madbi source rock was deposited under suboxic conditions in an open marine environment and this source rock is still within the oil window maturity range.  相似文献   

4.
Organic geochemical evaluation of thirty-two Aptian to Campanian shale samples from seven wells drilled on the shelf of the Orange Basin (southwestern Atlantic margin) was carried out in order to determine their origin, depositional environment, thermal maturity and hydrocarbon potential. The shale samples, selected to represent highstand, lowstand and transgressive systems tracts, were analysed by Rock–Eval pyrolysis for total organic C characteristics and by gas chromatography (GC) and gas chromatography–mass spectrometry (GC–MS) for n-alkanes, aliphatic isoprenoid hydrocarbons and biomarkers (steranes, hopanes and tricylic terpanes). For most of the shale samples Rock–Eval data, hydrogen (HI) and oxygen index (OI) point to mainly Type III terrigenous organic matter. Only a few samples of Turonian age reveal a higher proportion of marine organic matter being classified as Type II/III or Type II. Biomarker parameters suggest that the samples are deposited under suboxic to oxic environmental conditions. Rock–Eval data and biomarker maturity parameters assign for most of the samples a maturity level at the beginning of the oil window with some more mature samples of Aptian, Albian and Cenomanian age. The hydrocarbon generation potential is low for most of the shelf shales as indicated by the S2/S3 ratio and HI values. Exceptions are some samples of Turonian and Aptian age.  相似文献   

5.
Organic geochemical characterization of cutting samples from the Abu Hammad-1 and Matariya-1 wells elucidates the depositional environment and source rock potential of the Jurassic and Lower Cretaceous successions and the Middle Miocene to Pleistocene section in the southern and eastern Nile Delta Basin. The burial and thermal histories of the Mesozoic and Miocene sections were modeled using 1D basin modeling based on input data from the two wells. This study reveals fair to good gas-prone source rocks within the Upper Jurassic and Lower Cretaceous sections with total organic carbon (TOC) averaging 2.7% and hydrogen index (HI) up to 130 mg HC/g TOC. The pristane/n-C17 versus phytane/n-C18 correlation suggests mixed marine and terrestrial organic matter with predominant marine input. Burial and thermal history modeling reveals low thermal maturity due to low heat flow and thin overburden. These source rocks can generate gas in the western and northern parts of the basin where they are situated at deeper settings. In contrast, the thick Middle Miocene shows fair source rock quality (TOC averaging at 1.4%; HI maximizing at 183 mg HC/g TOC). The quality decreases towards the younger section where terrestrial organic matter is abundant. This section is similar to previously studied intervals in the eastern Nile Delta Basin but differs from equivalents in the central parts where the quality is better. Based on 1D modeling, the thick Middle Miocene source rocks just reached the oil generation stage, but microbial gas, however, is possible.  相似文献   

6.
Variations in the carbon isotopic composition (δ13C) of pristane, phytane, n-heptadecane (n-C17), C29 ααα 20R sterane, and aryl isoprenoids provide evidence for a diverse community of algal and bacterial organisms in organic matter of the Upper Ordovician Maquoketa Group of the Illinois Basin. Carbon isotopic compositions of pristane and phytane from the Maquoketa are positively covariant (r = 0.964), suggesting that these compounds were derived from a common source inferred to be primary producers (algae) from the oxygenated photic zone. A variation of 3‰ in δ13C values (−31 to −34‰) for pristane and phytane indicates that primary producers utilized variable sources of inorganic carbon. Average isotopic compositions of n-C17 (−32‰) and C29 ααα 20R sterane (−31‰) are enriched in 13C relative to pristane and phytane (−33‰) suggesting that these compounds were derived from a subordinate group of primary producers, most likely eukaryotic algae. In addition, a substantial enrichment of 13C in aryl isoprenoids (−14 to −18‰) and the identification of tetramethylbenzene in pyrolytic products of Maquoketa kerogen indicate a contribution from photosynthetic green sulfur bacteria to the organic matter. The presence of anaerobic, photosynthetic green sulfur bacteria in organic matter of the Maquoketa indicates that anoxic conditions extended into the photic zone.The δ13C of n-alkanes and the identification of an unusual suite of straight-chain n-alkylarenes in the m/z 133 fragmentograms of Ordovician rocks rich in Gloeocapsomorpha prisca (G. prisca) indicate that G. prisca did not contribute to the organic matter of the Maquoketa Group.  相似文献   

7.
The Namoi Formation in the Werrie Syncline, north and west of Tamworth, is part of the well-preserved Devonian–Carboniferous fore arc in the New England Fold Belt. The formation is between 640–914 m thick and consists of dominant olive-green mudstones with lenses of sandstone and oolitic limestone. To assess shale gas prospectivity, we analysed five outcrop samples from the Namoi Formation in the Keepit area. Well-preserved aliphatic and aromatic hydrocarbon fractions do not show evidence of weathering or biodegradation. n-Alkanes in all samples have a unimodal distribution maximising at C26 to C28. Little odd-to-even n-alkane carbon number predominance and relatively low Pr/n-C17 and Ph/n-C18 ratios are consistent with a high thermal maturity. Based on the distribution of alkylnaphthalenes and alkylphenanthrenes, the Namoi Formation is in the gas window. Calibration of the methylphenanthrene index and ratio with vitrinite reflectance suggests a calculated reflectance around 2.1%, which given a normal geothermal gradient is equivalent to a maximum temperature of 205°C for the deepest burial of the formation. There is a dominance of parent polycyclic aromatic hydrocarbons (PAH) over alkylated PAHs, supporting a high thermal maturity. Some samples contain biomarkers suggestive of a marine depositional environment, including the C30 sterane index and the C31/C30 hopane ratio. The Namoi Formation is a prospective shale-gas source, as it has been buried sufficiently to be well within the gas window. Where it is exposed at the surface gas will have been lost, but elsewhere it will be buried beneath other sediments and may still retain gas. Key exploration uncertainties include information on organic richness, lateral variation in thermal maturity, mineralogy, and porosity–permeability relationships.  相似文献   

8.
Aromatic hydrocarbons from benzene extracts of New Albany Shale were characterized. A biomarker that has a molecular weight of 546 and a structural configuration consistent with that of an alkyl-aromatic hydrocarbon (C40H66) was tentatively identified. It was found that the relative concentrations of the biomarker are indicative of differing levels of thermal maturity of the shale organic matter. A 40-carbon bicyclic carotenoid (C40H48) is proposed as the geochemical precursor of this biomarker. Thermal maturity of the shale organic matter can also be differentiated by observing differences in “fingerprints” as obtained by field-ionization mass spectrometry on the aromatic hydrocarbon fraction. Using this technique, we found that the more mature shale samples from southeastern Illinois contain more low molecular weight extractable aromatic hydrocarbons and the less mature shale samples from northwestern Illinois contain more high molecular weight extractable aromatic hydrocarbons. It was demonstrated that field-ionization and tandem mass spectrometric techniques through fingerprint and individual compound identification, are useful for shale aromatic hydrocarbon fraction characterization and for thermal maturation interpretation.  相似文献   

9.
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   

10.
The molecular organic compounds have been identified by gas chromatography (GC) and GC-mass spectrometry (GC-MS) from Mesoproterozoic rocks in the Xuanlong depression in North China. The main saturated compounds are n-alkanes, monomethylalkanes, n-alkylcyclohexanes, acyclic isoprenoids, and hopanes. The dominant lower-molecular-weight n-alkanes are indicative of the main contribution of microorganisms, in particular, the chemosynthetic bacteria. The presence of abundant monomethylalkanes (mid- and end-branched) and the long chained (>C20) acyclic isoprenoids indicates the existence of abundant bacteria and/or archaea in ancient oceans. The low abundance of pristane and phytane is suggestive of the relatively low abundance of photosynthetic autotrophs in comparison with chemosynthetic bacteria in the Mesoproterozoic oceans in North China. The sedimentary environmental condition is suboxic/anoxic, as indicated by the low value of the Pr/Ph ratio as well as the presence of abundant sulfur-bearing organic compounds, consistent with the other geochemical data in North China and elsewhere in the world. Both the composition of the primary producers and the sedimentary environmental conditions are favorable for the formation of hydrocarbon source rocks.  相似文献   

11.
The aliphatic fraction of the bitumens from 3 bands of the Puertollano oil shale field have been studied by gas chromatography and gas chromatography/mass spectrometry. Previous work published over the last years reached different conclusions about the origin of the organic matter in the Puertollano oil shales. A reappraisal of some of the biomarkers was then needed for a better understanding of the aliphatic hydrocarbons assemblage. The identified compounds, mainly n-alkanes in the medium to high boiling point region, acyclic isoprenoids and hopane-related compounds point towards a predominant algal/bacterial input. No unequivocally higher plant derived biomarkers have been detected in significant amounts, suggesting that the bulk of the organic matter derive from authocthonous organisms living in the basin. The biomarker maturity ratios indicate that the 3 Puertollano oil shales have similar maturities and are close to the onset of oil generation, assessing a slightly higher maturity than that determined by petrographic techniques.  相似文献   

12.
前寒武纪占了地球地质历史的八分之七,其地层中有机质的研究,是一个十分重要的领域。它主要包括两个方面的意义:一方面在于追踪地球早期历史的生物演化,企图为了解地球上生命起源和早期生命的特点提供信息;另外在于对前寒武纪、特别是晚前寒武纪地层中石油的兴趣。六十年代,G. Eglinton和M. Calvin提出了“化学化石”的概念。“化学化石”也叫做分子化石或“地球化学化石”。  相似文献   

13.
A geochemical study has been made of fine clay minerals and organic matter in subsurface shale samples from the Canadian Northwest Territories. The mixed layer clays comprise smectite-vermiculite-illite but are transformed during thermal diagenesis to a pseudo-quaternary system (smectitevermiculite-illite-chlorite) by incorporation of amorphous inorganic material. The first clay dehydration occurs prior to hydrocarbon generation and is accompanied by adsorption of K+ and substitution of Al3+ for Si4+ in the clay lattice. Vermiculite is an intermediary in the transformation of smectite to illite and in the presence of Ca2+ ions delays the second dehydration step to the zone where cracking of liquid hydrocarbons to gas occurs.Hydrocarbon generation commences at a vitrinite reflectance level of ? 0.5% R0 maximum in both amorphous and woody-herbaceous organic matter but does not reach a significant level in the latter case until reflectance levels of 0.7% R0 maximum. The pristane to phytane ratio and proportion of n-alkanes and acyclic isoprenoids increase during hydrocarbon generation from woody-herbaceous organic matter. Anomalous hydrocarbon yields from certain samples are attributed to high concentrations of plant resins. Destructions of liquid hydrocarbons by cracking commences at a reflectance level of 1.0% R0 maximum and is essentially complete by a reflectance level of 1.4% R0 maximum. The proportion of n-alkanes in the saturates decreases during cracking of the liquid hydrocarbons.  相似文献   

14.
A study of the influences of the basin brines on hydrocarbon generation of the Kupferschiefer in southwestern Poland has been carried out.The samples from the Konrad and Polkowics mines were analyzed by orgainc geochemical,microscopic and FTIR methods.The results indicate that organic matter of Kupferschiefer tends to decrease with the ascending,oxidizing brines,In the Konrad profile,the Kupferschiefer was strongly oxidized.The extract yields were depleted up to 50mg Ext/g Corg.Gas chromatography(GC) and gas chromatography-mass spctrometry(GC/MS) data indicate that the depletion occureed predominantly in saturated hydrocarbon compounds.The identified n-alkanes in smpale KD1 were depleted at least to 5000μg/g Corg.The aromatic compounds show a fidderent trend of variation.The concentrations of phenanthrene alkylphenanthrenes(Ph-PAH) and naphthalene alkylnaphthalenes(Na-PAH) show a decrease,whereas sulfur polyaromatic hydrocarbons(S-PAH)and oxygen polyaromatic hydrocarbons(O-PAH) show an incrase under the influences of oxidizing brines,In the Polkowice profile,organic matter under the influences of oxidizing fluids shows a simlar trend of varation as in the Konrad mine.Analyses of polar compounds shed light on the oxidation processes at the molecule level.The dominant products of oxidation are aliphatic acid.alcohol and ester.FTIR results indicate that the oxidation of organic matter led to a decrease in aliphatic CH3 and an increase in C-O,C=O bands.  相似文献   

15.
在四川盆地东部古生界地层发现大量天然气资源,鲜有原油发现。重庆天府磨心坡煤矿下二叠统茅口组石灰岩上部地层裂隙发现沿层间裂隙随水渗出的黄绿色液态轻质油苗。研究表明:油苗碳数分布较窄,为C4~C26,具有明显的姥鲛烷优势,Pr/Ph值为1.64,δ13C值为-26.2‰;油苗所反映的成熟度较高,折算Ro约为1.6%,一维盆地模拟验证二叠系的热演化程度可达与之相当的热演化程度。综合研究认为油苗与二叠系煤系地层关系密切。油苗的发现表明,在四川盆地古生界整体高过成熟的大背景下,某些成熟度相对较低,保存条件适宜的区域仍有发现一些中小型油藏的可能,这对四川乃至南方古生界油气勘探具有一定的启示意义。  相似文献   

16.
A petrological, organic geochemical and geochemical study was performed on coal samples from the Soko Mine, Soko Banja basin, Serbia. Ten coal and two carbonaceous clay samples were collected from fresh, working faces in the underground brown coal mine from different parts of the main coal seam. The Lower Miocene, low-rank coal of the Soko Mine is a typical humic coal with huminite concentrations of up to 76.2 vol.%, liptinite less than 14 vol.% and inertinite less than 11 vol.%. Ulminite is the most abundant maceral with variable amounts of densinite and clay minerals. Sporinite and resinite are the most common macerals of the liptinite group. Inertodetrinite is the most abundant maceral of the inertinite group. The mineral-bituminous groundmass identified in some coal samples, and carbonaceous marly clay, indicate sub-aquatic origin and strong bacterial decomposition. The mean random huminite reflectance (ulminite B) for the main coal seam is 0.40 ± 0.05% Rr, which is typical for an immature to early mature stage of organic matter.The extract yields from the coal of the Soko Banja basin ranges from 9413 to 14,096 ppm, in which alkanes constituted 1.0–20.1%, aromatics 1.3–14.7%, asphaltenes 28.1–76.2% and resins 20.2–43.5%. The saturated hydrocarbon fractions included n-C15 to n-C32, with an odd carbon number that predominate in almost all the samples. The contents of n-C27 and n-C29 alkanes are extremely high in some samples, as a contribution of epicuticular waxes from higher plants. Acyclic isoprenoid hydrocarbons are minor constituents in the aliphatic fraction, and the pristane/phytane (Pr/Ph) ratio varies between 0.56 and 3.13, which implies anaerobic to oxic conditions during sedimentation. The most abundant diterpanes were abietane, dehydroabietane and 16α(H)-phyllocladane. In samples from the upper part of the coal seam, diterpanes are the dominant constituents of the alkane fraction. Polycyclic alkanes of the triterpane type are important constituents of alkane fractions. The occurrence of ββ- and αβ-type hopanes from C27 to C31, but without C28, is typical for the Soko Banja coals.The major and trace elements in the coal were analysed using X-ray fluorescence (XRF), and inductively coupled plasma-mass spectrometry (ICP-MS). In comparison with world lignites, using the geometric mean value, the coal from the Soko Banja Basin has a high content of strontium (306.953 mg/kg). Higher values than the world lignites were obtained for Mo (3.614 mg/kg), Ni (8.119 mg/kg), Se (0.884 mg/kg), U (2.642 mg/kg) and W (0.148 mg/kg). Correlation analysis shows inorganic affinity for almost all the major and trace elements, except for S, which has an organic affinity.  相似文献   

17.
The stable hydrogen isotopic compositions (δD) of selected aliphatic hydrocarbons (n-alkanes and isoprenoids) in eight crude oils of similar source and thermal maturity from the Upper Indus Basin (Pakistan) were measured. The oils are derived from a source rock deposited in a shallow marine environment. The low level of biodegradation under natural reservoir conditions was established on the basis of biomarker and aromatic hydrocarbon distributions. A plot of pristane/n-C17 alkane (Pr/n-C17) and/or phytane/n-C18 alkane (Ph/n-C18) ratios against American Petroleum Institute (API) gravity shows an inverse correlation. High Pr/n-C17 and Ph/n-C18 values and low API gravity values in some of the oils are consistent with relatively low levels of biodegradation. For the same oils, δD values for the n-alkanes relative to the isoprenoids are enriched in deuterium (D). The data are consistent with the removal of D-depleted low molecular weight (LMW) n-alkanes (C14–C22) from the oils. The δD values of isoprenoids do not change with progressive biodegradation and are similar for all the samples. The average D enrichment for n-alkanes with respect to the isoprenoids is found to be as much as 35‰ for the most biodegraded sample. For example, the moderately biodegraded oils show an unresolved complex mixture (UCM), loss of LMW n-alkanes (<C15) and moderate changes in the alkyl naphthalene distributions. The relative susceptibility of alkyl naphthalenes at low levels of biodegradation is discussed. The alkyl naphthalene biodegradation ratios were determined to assess the effect of biodegradation. The dimethyl, trimethyl and tetramethyl naphthalene biodegradation ratios show significant differences with increasing extent of biodegradation.  相似文献   

18.
Oil shales were deposited in the Songliao Basin (NE China) during the Upper Cretaceous period, representing excellent hydrocarbon source rocks. High organic matter (OM) contents, a predominance of type-I kerogen, and a low maturity of OM in the oil shales are indicated by bulk geochemical parameters and biomarker data. A major contribution of aquatic organisms and minor inputs from terrigenous land plants to OM input are indicated by n-alkane distribution patterns, composition of steroids, and organic macerals. Strongly reducing bottom water conditions during the deposition of the oil shale sequences are indicated by low pristane/phytane ratios, high C14-aryl-isoprenoid contents, homohopane distribution patterns, and high V/Ni ratios. Enhanced salinity stratification with mesosaline and alkaline bottom waters during deposition of the oil shales are indicated by high gammacerane index values, low MTTC ratios, high β-carotene contents, low TOC/S ratios, and high Sr/Ba ratios. The stratified water column with anoxic conditions in the bottom water enhanced preservation of OM. Moderate input of detrital minerals during the deposition of the oil shale sequences is reflected by titanium concentrations. In this study, environmental conditions in the paleo-lake leading to OM accumulation in the sediments are related to sequence stratigraphy governed by climate and tectonics. The first Member of the Qingshankou Formation (K2qn1) in the Songliao Basin, containing the oil shale sequence, encompasses a third-order sequence that can be divided into three system tracts (transgressive system tract—TST, highstand system tract—HST, and regressive system tract—RST). Enrichment of OM changed from low values during TST-I to high-moderate values during TST-II/III and HST-I/II. Low OM enrichment occurs during RST-I and RST-II. Therefore, the highest enrichment of OM in the sediments is related to stages of mid-late TST and early HST.  相似文献   

19.
A consequence of the biodegradation of petroleum is that lower molecular weight compounds are removed preferentially to higher molecular weight (HMW) compounds greater than triacontane (n-C30). The extent to which the latter compounds are biodegraded has rarely been studied. Reasons for this include the technical difficulties associated with carrying out biodegradability tests with solid, water-insoluble substances and the limits of the analytical techniques, such as gas chromatography (GC).A quantitative high temperature GC (HTGC) method was developed to monitor the biodegradation of the aliphatic fraction of a waxy Indonesian oil by Pseudomonas fluorescens. Recoveries of over 90% were obtained for n-alkanes up to hexacontane (C60) using liquid-liquid continuous extraction. After only 14 days, 80% of the aliphatic hydrocarbons had been degraded. At the end of the 136-day study, 14% of the original fraction remained. This comprised mainly C40+ compounds. No decrease in the concentrations of compounds above C45 was observed. However, the use of a rapid screening biodegradation method provided tentative proof that Pseudomonas fluorescens was capable of utilising n-alkanes up to C60 once the bacteria had acclimated to HMW alkanes.  相似文献   

20.
Currently, the presence of free n-alkanes and isoprenoid alkanes in carbonaceous meteorites is usually explained either by microbial contamination during the period between the meteorite fall and collection or by contamination from the environment of analytical laboratories and museums. The goal of this research was to repeat analysis of hydrocarbon components in meteorites and to investigate possible meteorite contamination routes discussed in the literature. Experimental analysis of free organic constituents in five carbonaceous meteorites by infrared spectroscopy (IR) and gas chromatographic (GC) methods confirmed the presence of extractable aliphatic components, n-alkanes in the C15H32-C27H56 range and isoprenoid alkanes (phytane, pristane, and norpristane), in some of these meteorites. The contents of these compounds vary depending on the source. Insoluble organic components of two meteorites (meteorite kerogens) were isolated, and their composition was analyzed by IR and cracking/GC methods. Comparison with the data on several terrestrial contamination sources proposed in the literature shows that the presence of free saturated hydrocarbons in meteorites and the composition of the meteorite kerogen could not be explained either by microbial contamination or by contamination from the laboratory environment. The types of the hydrocarbons in meteorites resemble those typical of ancient terrestrial deposits of organic-rich sediments, except for the absence of lighter hydrocarbons, which apparently slowly evaporated in space, and multi-ring naphthenic compounds of the biologic origin, steranes, terpanes, etc. The prevailing current explanation for the presence of free linear saturated hydrocarbons in carbonaceous meteorites, apart from contamination, is the abiotic route from hydrogen and carbon monoxide. However, the data on the structure of meteorite kerogens require a search for different routes that initially produce complex polymeric structures containing n-alkyl and isoprenoid chains which are attached, via polar links (esters, salts, etc.), to a cross-linked polymer matrix. Later, the polymer slowly decomposes with the liberation of free aliphatic hydrocarbons.  相似文献   

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