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1.
三塘湖盆地上二叠统芦草沟组烃源岩地球化学特征   总被引：3，自引：0，他引：3  
三塘湖盆地上二叠统芦草沟组分布面积广、厚度大、有机碳含量高,具好的生烃潜力,是盆地内主力烃源岩。烃源岩样品可溶有机质中含有丰富的脂肪酸、脂肪酸酯等含羰基化合物,随着埋深增加,饱和烃和芳烃含量递增,非烃含量和有机碳则呈递减趋势,表明含羰基化合物对源岩生烃有较大的贡献。饱和烃的各项指标显示,烃源岩的沉积环境为咸化湖相还原环境,母质输入以水生生物为主,陆源物质输入较少。诸多证据表明,在沉积初期和成岩早期细菌输入较多,细菌输入有机质构成了原始有机质的一部分,细菌改造原始有机质并产生前述含羰基化合物,在热作用和微生物作用下均可成烃。  相似文献   

2.
Diatomaceous ooze of the shelf off Walvis Bay (S.W. Africa) was analysed for lipid material. The lipids from the sediment consist of a mixture of hydrocarbons, alcohols, ketones, fatty acids, sterols, carotenoid pigments and chlorophylls. The total fatty acid mixture has been analysed by capillary gas chromatography mass spectrometry and shown to consist of straight chain, iso-, anteiso- and isoprenoid acids. The environmental setting of the S.W. African shelf (Walvis Bay) makes it possible to discuss these fatty acids as markers for the fate of organic matter. The acids in the sediment point to a generation during passage of algal lipids through levels of microbial activity either on or slightly above the burial surface.  相似文献   

3.
This paper consists of two interrelated parts. In the first part, the influence of the composition of sediment organic matter on crude oil composition is discussed. The second part deals with the origin of normal paraffins in petroleum.Source beds with abundant terrestrial plant matter generate heavy hydrocarbons rich in five-ring naphthenes. Unless such source beds are exposed to a high temperature for a prolonged time, the oils released are also rich in five-ring naphthenes. Such oils are rare; thus far the only examples found are some Eocene Wilcox oils from the Texas Gulf Coast and some Eocene Green River oils from the Uinta Basin, Utah. Normally, oil source beds are not rich in terrestrial plant matter and the five-ring naphthene content of the source bed hydrocarbons, as well as that of the produced oils, is low.The n-paraffins generated by oil source beds rich in terrestrial plant matter are characterized by abnormally low (C21 + C22)/(C28 + C29) ratios of 0.6–1.2. In oils of dominantly marine origin, this ratio is in the range 1.5–5.0. The ratio of marine to terrestrial organic matter in source beds appears to influence both the naphthene composition and the n-paraffin composition of the generated oils.Evidence is presented that petroleum n-parainns originate from slow thermal cracking of fatty acids contained in fats and waxes. Reaction equations are discussed which explain the major geochemical observations, including the difference in carbon-number distribution of the assumed parental fatty acids and of their descendant n-paraffins. In normal oils, which originate mostly from fat rich marine organic matter, the n-paraffin concentration tapers off above C20. The molecular weight range of the fatty acids of plant waxes is considerably higher than that of fats. If plant waxes contribute strongly to the oil source material, the molecular weight distribution of the petroleum n-paraffins formed is abnormal and high carbon numbers in the C24-C32 range dominate.  相似文献   

4.
Benzene extractable aliphatic hydrocarbons from the New Albany Shale in the Illinois Basin were characterized by gas chromatography and mass spectrometry, and the total organic matter of the shale was characterized by solid state carbon-13 cross polarization magic angle spinning nuclear magnetic resonance. Core samples from a northwest-trending cross-section of the Illinois Basin were studied. Gas chromatography (GC) and gas chromatography-mass spectrometric analysis (GC/MS) data indicate a regional variation of the aliphatic composition of the shale extracts. A positive, linear relationship between the two ratios, pristane/n-C17 and phytane/n-C18, is indicated. The NMR results indicated that organic matter deposited in northwestern Illinois shale is relatively high in aliphatic hydrocarbon content while, in contrast, organic matter found in southeastern Illinois shale is relatively low in aliphatic hydrocarbon content. Our findings suggest that the organic variation of the shale is mainly due to the differences in thermal maturity of the shale organic matter and the use of pristane/n-C17 ratio as a thermal parameter in the study of oil may be extended to the study of the ancient sediments.  相似文献   

5.
In order to improve understanding of the stratigraphy of the Lake Turkana Basin, one of the important sites in the evolution of early man, this study evaluates the usefulness of organic biological marker compounds, n-alkanes and fatty acids, for correlation of isolated sedimentary strata.Eighty-five paleosol samples were collected from well-defined sedimentary horizons in two regions (Area 103 and Area 130) of the Koobi Fora area of Lake Turkana. Results indicate that most of the organic matter present was derived from terrestrial plant waxes. In sediments where extensive diagenesis has occurred, microbial input of organic matter may have been substantial. Algae were either not an important source of organic matter, or their marker compounds have been removed or altered by degradative processes.The fate of the original paleosol organic matter has been governed to some extent by weathering processes, especially in Area 130. Weathering decreased the amount of extractable lipids, particularly fatty acids and the low molecular weight alkanes (C17C20); produced or retained relatively large amounts of alkanes greater than C21 within a unimodal distribution; and lowered CPI values. Consequently, stratigraphic correlation by unique alkane and fatty acid distributions has been confined to short distances (many meters).Both n-alkanes and fatty acids have been retained better by association with clay minerals than by sand matrices. The alkane distribution of sandstones differs from that of clay organics in having a narrower carbon chain length distribution and lower CPI values. In Area 103, where weathering was less severe, compositional variations with stratigraphic position indicate that lipid material has been retained within each of the facies examined.  相似文献   

6.
A rank series of lignites and coals of low to moderate maturation levels (vitrinite reflectance (R0): 0.27–0.8%) from the New Zealand Coal Band were investigated using alkaline ester cleavage experiments to reveal compositional changes of ester bound components (fatty acids and alcohols) during increasing maturation. Ester bound alcohols are found to be present in highest amounts in the very immature lignite samples (R0: 0.27–0.29%), but show a rapid decrease during early diagenesis. Ester bound fatty acids also show an initial exponential decrease during diagenesis, but reveal an intermittent increase during early catagenesis before decreasing again during main catagenesis. This intermittent increase was related to the short chain fatty acids. To obtain a maturity related signal and to eliminate facies related scattering in the amounts of fatty acids in the coal samples, the carbon preference index of fatty acids (CPIFA) parameter is introduced here. For the long chain fatty acids (C20–C32) originating from terrigenous plant debris, the CPIFA decreases with increasing maturity, showing a strong maturation related signal. During diagenesis, the same trend can be observed for the short chain fatty acids, but the intermittent increase in the amounts of short chain fatty acids is also accompanied by high CPIFA values. This indicates less altered organic biomass at this advanced maturation level and is in contrast to the mature CPIFA signal of the long chain fatty acids of the same samples. One possible reason for this discrepancy could be extremely different amounts of short and long chain fatty acids in the original source organic matter of these samples. However, another intriguing explanation could be the incorporation of immature bacterial biomass from deep microbial communities containing C16 and C18 fatty acids as main cell membrane components. Deep microbial life might be stimulated at this interval by the increasing release of thermally generated potential substrates from the organic matrix during early catagenesis. In contrast to the fatty acids, the high amounts of alcohols in the immature lignite samples are also visible in the alkene distribution from the open system pyrolysis experiments of the organic matrix before and after saponification.  相似文献   

7.
The lipid components in hydrothermal sulfide deposits from the Rainbow vent field (Mid-Atlantic Ridge at 36°N) were studied by gas chromatography/mass spectrometry. The Rainbow vent field is one of two known active hydrothermal systems related to abyssal circulation, where high-temperature fluids are formed during serpentinization of ultrabasic crustal rocks. The major amount of the extractable organic matter from the sulfides consists of normal and branched alkanes, UCM, PAHs, terpenoids, and fatty acids. The branched alkanes are comprised of unique gem-diethylalkane series, possibly from sulfide oxidizing bacteria, and biphytanes from archaea. The characteristic lipid and biomarker compounds found in the hydrothermal samples support a predominantly biological origin of the bitumens from the thermal transformation of the biomass of microorganisms (bacteria and archea) and minor macrofauna of this vent field. A search for molecular evidence for abiogenic thermocatalytic synthesis of organic compounds was negative. However, methane in the hydrothermal fluids and possibly a minor amount of the alkanes in the sulfides may be of an abiogenic origin in the Rainbow vent field.  相似文献   

8.
As geochemical appraisals of mineral regions of commercial prospectivity evolve, the organic matter associated with metal rich ores has attracted greater attention. Petroleum basin and modern seafloor hydrothermal vent studies have suggested that organic matter can have a significant influence on the behaviour of mineralising fluids. There have been many isolated reports of certain organic compositional or morphological (e.g. pyrobitumen) features showing an apparent relationships with hydrothermal fluids or minerals, raising expectations that organic based parameters might be useful to mineral exploration. However, the understanding of organic–inorganic relationships in Earth systems is far from complete. For example, the detailed mechanics of the interaction of organics with hydrothermal fluids over geological time remain largely undefined. Organic geochemistry studies have traditionally involved the measurement and interpretation of the hydrocarbon composition of sedimentary rocks. Here we review the types of aliphatic hydrocarbons, aromatic hydrocarbons and metalloporphyrins often detected from organic geochemical investigations in mineral-rich regions. Such molecular data can be particularly diagnostic of biochemical sources and the palaeo-environments at the time mineral associated organic matter was deposited. Sub-surface trends of hydrocarbon alteration may also reflect major biogeochemical processes such as thermal maturity and biodegradation. Organic geochemistry data can also occasionally provide information about the nature (e.g., origin, composition, temperatures) and migration pathways of hydrothermal fluids and can make a contribution to holistic ore genesis models. The well preserved organic matter associated with the economic “Here's Your Chance” Pb–Zn–Ag Mine (Paleoproterozoic Barney Creek Formation, McArthur Basin, Australia) and the transition metal-rich Early Permian Kupferschiefer Formation (Germany–Poland) have attracted significant attention. A more detailed summary of the organic character of these deposits is provided to highlight the contribution organic geochemistry can make to understanding mineralisation processes. Most organic geochemical studies of highly mineralised regions, however, have not adequately addressed the significance of organic matter to mineralisation. A slightly different analytical focus than traditionally used for exploration appraisal of petroleum hydrocarbons may be required to properly evaluate the significance of organic species to the mobilisation, transport and deposition of ore metals. The characterisation and subsequent thermodynamic modeling of organic substances and complexes within metalliferous hydrothermal systems will contribute to a better understanding of the nature and role of organic–inorganic fluids or other affiliated organics in ore systems.  相似文献   

9.
Particulate matter was collected during September–October, 1977, in particle traps suspended 30–60 m above the floor of San Nicolas, Santa Barbara, Santa Monica and San Pedro Basins, off the coast of southern California. The trap particulates were analyzed for C15–C35 hydrocarbons using gas chromatography (GC) and GC-mass spectrometry. Kerogens and humic acids were characterized by H/C, N/C, δ13C, δ15N and δ34S ratios, and by electron-spin resonance. Hydrocarbons arising from fresh and weathered petroleum, marine autochthonous and terrestrial sources were identified. The rates of petroleum deposition during the collection period followed the order: San Nicolas Basin < Santa Barbara Basin ~ Santa Monica Basin < San Pedro Basin, with the largest amount of weathered petroleum being deposited in San Pedro Basin. The rates of petroleum deposition are correlated more strongly with human activities such as shipping, and the discharge of municipal and industrial wastes, than with natural submarine oil seepage. Analyses of kerogens and humic acids indicate that the majority of the organic matter in the trap particulates is of marine origin. The water column overlying Santa Barbara Basin appears to have the highest marine productivity of the four basins studied.  相似文献   

10.
The first building blocks of life could be produced in ultramafic-hosted hydrothermal systems considering the large amounts of hydrogen and methane generated by serpentinisation and Fischer–Tropsch-Type synthesis, respectively, in those systems. The purpose of this study was to detect and characterise organic molecules in hydrothermal fluids from ultramafic-hosted hydrothermal systems in the Mid-Atlantic Ridge (MAR) region. During the EXOMAR cruise 2005, fluids from the Rainbow (36°14′N) and the Lost City (30°N) hydrothermal fields were collected and treated by Stir Bar Sorptive Extraction (SBSE) and Solid Phase Extraction (SPE). The extracts were analysed by Thermal Desorption–Gas Chromatography–Mass Spectrometry (TD–GC–MS) and GC–MS, respectively. Compared to nearby deep seawater, hydrothermal fluids were clearly enriched in organic compounds, with a more diverse spectrum of molecules. We observed a very similar range of organic compounds in fluids from both sites, with a dominance of aliphatic hydrocarbons (C9–C14), aromatic compounds (C6–C16) and carboxylic acids (C8–C18). The occurrence of these compounds is supported by other field studies on serpentinites and sulfide deposits. Literature on thermodynamic data and experimental work has suggested the possible abiogenic origin of hydrocarbons and organic acids. In addition, it has been shown elsewhere that catalytic reactions producing hydrocarbons likely occur at both Lost City and Rainbow hydrothermal fields as suggested by the evolution of δ13C with increasing C number for methane, ethane, propane and butane. In order to investigate the origin of the organic molecules in the fluids, compound-specific carbon isotope ratio measurements were performed on n-alkanes and carboxylic acids, for which the δ13C values were in the range of ? 46 to ? 20‰ (vs. V-PDB). These preliminary data did not allow conclusive support or rejection of an abiogenic origin of the compounds. Indeed, predicting δ13C signatures in hydrothermal systems is likely to be complicated, due to differences in source δ13C signatures (i.e., of the C building blocks), and a variety of, mostly unknown, fractionation steps which may occur along the synthesis pathways. In addition, even though a fraction of the compounds detected in the fluids is likely abiotically produced, a dominance of biogenic sources and/or processes might hide their characteristic signature.  相似文献   

11.
Sedimentary organic matter in hydrothermal systems can be altered by high temperature fluids to generate petroleum. The saturated and aromatic fractions of these hydrothermal oils are compositionally similar to conventional oil with the exception that they often contain higher concentrations of polycyclic aromatic hydrocarbons (PAH) as well as substantial mixtures of coeluting organic compounds that produce dramatically rising signal on the baseline of gas chromatograms termed unresolved complex mixtures (UCMs). Little is known about the compounds that compose UCMs and why or how they form. This is in part due to an inability to discriminate between in situ and migrated components that characterize the petroleum generated in hydrothermal systems. However, UCMs are also a product of the limitations imbedded in analytical separation techniques. With the advent of comprehensive two-dimensional gas chromatography (GC × GC), a revision of what should constitute molecular complexity needs to be considered. We address these problems by comparing the molecular compositions of the maltene fractions of three previously published hydrothermal petroleum samples using time of flight-mass spectrometry (GC × GC–ToF-MS) and 12 hydrothermal petroleum samples in cores from three locales using comprehensive two-dimensional gas chromatography with flame ionization detection (GC × GC–FID). The sediment cores were collected from Middle Valley, located off the axis of the Juan de Fuca Ridge, and the Escanaba Trough, along the Gorda Ridge, both in the NE Pacific Ocean, as well as from the Guaymas Basin in the Gulf of California. We define a UCM in GC × GC data to be a condition in which ⩾25% of the detected peaks within a chromatographic area coelute in either the first or second dimension. In turn, complex (CM) and simple mixtures (SM) are defined as having 5–24% and <5% coelution, respectively. All CM and UCMs were dominated by an array of configurational isomers, which becomes increasingly aromatic with higher molecular weight. We relate this to a multi-molecular complexity metric (MCM) by quantitatively comparing the difference in total peak variance and peak density for a GC × GC chromatogram. MCM values correlate with biomarker thermal maturity ratios for the Escanaba Trough and Guaymas Basin samples indicating that molecular complexity in these hydrothermal environments is in part a function of burial temperatures. Partial Least Squares (PLS) linear regression was applied to the total number of peak retention times as a proxy for the bulk molecular differences between each hydrothermal oil sample. Differences in the sample regressions correlate with the thermal maturity and the degree of PAH alkylation, indicating that this technique can be used to assess the degree of oxidative weathering due to dehydrogenation and hydrocarbon cracking. Subtracted chromatograms were then used to quantitatively track all of the individual molecular changes within the pyrolytic regime at Escanaba Trough. These subtracted chromatograms indicate that high molecular weight PAHs are highly mobile in hydrothermal fluids and may represent a phase partitioning that is occurring at greater depths. This phase condenses just below the seafloor to form an UCM in the near surface sediments. Saturated hydrocarbon biomarkers, such as hopanes, steranes and biphytanes are less mobile and more prone to being cracked and/or aromatized prior to migration toward the ocean floor. Together these techniques suggest that the molecular complexity of hydrothermal petroleum maximizes during the early stages of thermal maturation. The diversity of compounds forming these UCMs then decreases with increasing dehydrogenation, dealkylation and condensation reactions associated with elevated thermal stress and exposure to oxidants within the hydrothermal fluids.  相似文献   

12.
Two wells, Balazuc (BA1) and Morte-Mérie (MM1), located in a confined area (1200 m apart) and separated by the Uzer fault (a Liassic structure with a dip fault of 1300 m) were analysed using conventional methodologies and techniques (PRV, TAI, XRD, STEM) in order to compare the diagenetic evolution of clays and organic matter. The thermal convective process allows the circulation of hot fluids and the oxidation of organic matter. The conductive process allows the maturation of the organic matter, the expulsion of hydrocarbons and the deposit of pyrobitumes in the migration channels. To cite this article: L. Martinez et al., C. R. Geoscience 334 (2002) 1021–1028.  相似文献   

13.
Fifteen sediment samples were studied from five drill sites recovered by the ‘Glomar Challenger’ on Legs I and IV in the Gulf of Mexico and western Atlantic. This study concentrated on compounds derived from biogenic precursors, namely: (1) hydrocarbons, (2) fatty acids, (3) pigments and (4) amino acids.Carbon isotope (δC13) data (values < ? 26%, relative to PDB), long-chain n-alkyl hydrocarbons ( ?C277) with odd carbon numbered molecules dominating even carbon numbered species, and presence of perylene proved useful as possible indicators for terrigenous contributions to the organic matter in some samples. Apparently land-derived organic matter can be transported for distances over 1000 km into the ocean and their source still recognized.The study was primarily designed to investigate: (i) the sources of the organic matter present in the sediment, (ii) their stability with time of accumulation and (iii) the conditions necessary for in situ formation of new compounds.  相似文献   

14.
Minerals might act as important sorbents of sedimentary organic matter and reduce biodegradation, which favors the formation of hydrocarbon source rocks in the earth's history. Since most organic matter is degraded during the sinking process, at ambient temperature, it is important to investigate the adsorption capacity of different minerals during this process, to assess the organic loss from primary productivity to sedimentary organic matter. In this study, montmorillonite and calcite have been selected to study the impact of different minerals on the release, adsorption, and deposition of cyanobacterial (Synechococcus elonpata) fatty acids (FAs) at ambient temperature. Gas chromatography (GC), gas chromatography-mass spectrometry (GC-MS) have been utilized to detect the variation in fatty acids. Primary results suggest that minerals have a different impact on dissolved organic matter. Montmorillonite can specifically enhance the release of fatty acids from cyanobacterial cells by lowering the pH values of the solution. The adsorption of the dissolved organic matter by montmorillonite will also be enhanced under a lower pH value. Conjunction of fatty acids with montmorillonite to form a complex will favor the sinking and preservation of these organics. Selective adsorption is observed among fatty acids with different carbon numbers. In contrast, calcite does not show any impact on the release and adsorption of organic matter even though it is reportedly capable of acting as a catalyst during the transformation of organic matter at high temperature. The primary data bridge a link between primary productivity and sedimentary organic matter, suggesting the relative importance of claystones in the formation of hydrocarbon source rocks in the earth's history.  相似文献   

15.
Soluble organic matter had been separated from several palygorskite and bentonite samples in the Ji-angsu-Anhui border area(across Jiangsu Province and Anhui Province) and Linze County in Gansu Province of China and was analyzed with the techniques and methods of organic geochemistry.The composition and distribution of hydrocarbons were analyzed by gas chromatography(GC).Organic stable carbon isotopic ratios(δ13C) in typical samples were determined.The abundance of soluble organic matter in all clay samples analyzed was low.In Ji-angsu-Anhui samples,the preservation states of organic matter are different;hydrocarbons in organic matter have some features of aquatic plankton but are short of the input of terrigenous higher plants;organic δ13C in a palygor-skite of Yongxiaoshan in Xuyi County,Jiangsu Province,is-6.72‰.These features may be typical of a sedimentary environment of closed or semi-closed and relatively isolated different waters near coast or seashore.On the contrary,in samples from Gansu,the preservation states of organic matter are good;the GC graphs of hydrocarbons show that the precursors of the organic matter are from a mixed source of aquatic organisms and land-sourced higher plants;organic δ13C of a palygorskite from Yangtai of Gansu is-15.62‰.It indicated that the sedimentary environment may be an inland salty lake.Preliminary results suggest that palygorskite minerals in the Jiangsu-Anhui area may be evolved from rapidly accumulated fine material or volcanic ash,but clays in Gansu Province may be transformed from terrigenous inorganic clastic components carried to the lake through river and then deposited.The generation process of the samples studied in the paper seems to be related to salty water.  相似文献   

16.
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   

17.
认识沉积环境有机碳留存状况是阐述油气形成过程中有机碳早期成岩的关键内容。以南海珠江口盆地及其邻近海域为背景,通过研究表层沉积物中脂类化合物的形态组成,认识脂类有机碳的来源和留存状态,阐述特征脂类分子的早期成岩特征。结果表明,研究区域表层沉积物有机碳含量为0.22%～0.66%,有机碳稳定同位素分布在-20.88‰～-22.93‰之间,表现为显著的海源特征。沉积物中共检测出21种脂肪酸、6种脂肪醇、8种甾醇和植醇;总脂肪酸、脂肪醇、甾醇和植醇含量分别为12.57～40.27μg/g、5.35～8.98μg/g、0.15～3.75μg/g和0.01～3.99μg/g干重,总体表现为靠近珠江口和台湾海峡略高。脂类化合物的存在形态以游离态(FR)和碱性水解态(BH)为主,酸性水解态(AH)贡献较低;其中植醇和甾醇呈现显著的BH优势,植醇中未检出AH组分的贡献。脂类化合物主要来自于海洋现场生产,海洋微藻和细菌的相对贡献率分别为21.18%～33.78%和11.02%～15.64%,陆源高等植物贡献低于5%。来源于硫酸盐还原菌的支链脂肪酸在靠近珠江口海域高达1.79～2.62μg/g,占总脂肪酸的5.14%～6.50%,并与硫酸盐还原过程相关的古菌分布相一致。  相似文献   

18.
Changes in organic materials preserved within sediments of Saginaw Bay deposited over the past two centuries record corresponding periods in the environmental history of this part of Lake Huron and its watershed. Sediments deposited since 1940 show an increasingly greater input of aquatic organic matter in response to accelerating cultural eutrophication of Saginaw Bay. Concentrations of fatty acids, sterols, fatty alcohols, and aliphatic hydrocarbons are higher in these modern sediments than in deeper ones. Molecular distributions of these geolipids reflect less aquatic material deeper in the sediments. Prior to 1875, sediment organic matter appears to be diluted by mineral matter from enhanced erosion caused by clearing of the watershed for farming and settlement. During this period there is better preservation of carbonate minerals due to quicker burial. Since 1875, petroleum components comprise over 90% of the total aliphatic hydrocarbon content of these sediments, reflecting the advent and continued existence of chronic, low-level petroleum contamination of this part of the Great Lakes.  相似文献   

19.
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   

20.
Representative samples of crude oils from Cusiana, Cupiagua, Apiay, Castilla and Chichimene fields in the Eastern Llanos Basin of Colombia were analyzed to determine its compound-specific stable carbon isotope composition (CSIA) using gas chromatography–isotopic ratio–mass spectrometry (GC–IRMS). GC–IRMS analyses of n-alkanes allowed differentiating between Cretaceous and Cretaceous/Tertiary oil samples. Cretaceous sourced samples have δ13C-enriched values than Cretaceous/Tertiary sourced samples; the heavier isotope composition of these samples is due to their major terrigenous organic matter input. Their isotope distribution patterns suggest significant algal and/or bacterial contribution (marine origin). The analysis of the n-alkane fractions by GC–IRMS confirms that the organic matter has marine origin in those samples from Cusiana, Cupiagua and Apiay while Castilla and Chichimene have marine origin with terrestrial inputs. The results were confirmed by gas chromatography/FID and gas chromatography/mass spectrometry (GC/MS). Basic geochemical composition show that samples from Cupiagua/Cusiana fields and Apiay/Castilla/Chichimene fields in the Llanos basin, Colombia present different characteristics reflecting a specific for each depositional environment.  相似文献   

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