Pyrolysis of Transvaal kerogens. II. An evaluation of vacuum pyrolysis with polyethylene,polystyrene and their mixtures with minerals

A series of experiments have been conducted with polyethylene and polystyrene standards in an attempt to define the advantages and limitations of a vacuum pyrolysis—gas chromatography—mass spectrometry procedure for the characterization of kerogen and other macromolecular substances. Effects of variations in pyrolysis temperatures and times, sample sizes (weights) and thickness were evaluated together with the reproducibility of the nature and abundances of pyrolyzates. The effects of minerals (illite and quartz) admixed in the polymers were also considered with reference to the nature of the breakdown products. Optimal pyrolysis conditions, where primary pyrolyzates were sufficiently abundant and secondary products did not hinder characterization, were attained at 450°C and 60–90 min. The reproducibility of the nature and quantities of pyrolyzates was rather satisfactory at this temperature and pyrolysis time. However, relatively large samples of macromolecular matter, which is considerably volatile at this temperature, led to the synthesis of an abundant yield of secondary products, but sample thickness does not affect the nature of pyrolyzates. Admixed mineral matter affected the nature and relative abundances of the pyrolyzates but did not impede characterization of samples, as primary breakdown products were discernible. Macromolecular substances of limited volatility, heterogeneous chemical composition and containing intractable mineral matter, such as many kerogens, need to be pyrolyzed as relatively large samples. The vacuum procedure used in these studies may be to advantage, as compared with some other methods, to pyrolyze such samples. This method seems to be also suitable for the pyrolysis of volatile macromolecular matter, provided that small samples are employed.     

Modeling of catagenetic transformation of organic matter from a Riphean mudstone in hydrous pyrolysis experiments: Biomarker data

The catagenesis of organic matter (OM) was modeled by the hydrous pyrolysis of a Riphean mudstone. Microscopic observations of the processes operating during kerogen heating to 600°C were conducted in a diamond anvil cell. The results of pyrolysis in an aqueous environment were used to calculate the activation energies of kerogen cracking and derive chemical kinetic models for OM catagenesis. Isothermal experiments were carried out for 3 days at temperatures of 300, 310, …, 360, and 370°C. The maximum bitumen yield was obtained at 330°C followed by thermal cracking at higher temperatures. The aromatic and saturated hydrocarbons from rock bitumen, hydrous pyrolyzates, and kerogen flash pyrolyzates were analyzed by chromatography-mass spectrometry. We also discuss the problem of extrapolation of high-temperature pyrolysis results to geologic observations under the conditions of regional catagenesis.     

Proteins as a possible source material of low molecular weight petroleum hydrocarbons

Low temperature cracking experiments of a representative protein, at temperatures not far above the observed temperature range of 130–160°C of mature California oil source rocks, indicate the formation of all gaseous and of some gasoline range hydrocarbons of petroleum. Based on protein derivatives only it is estimated that a maximum of at least 3–8% by weight of the total organic matter of oil source sediments may be converted into such hydrocarbons. This is in addition to hydrocarbons originating from lipids.     

Methane adsorption in the low–middle-matured Neoproterozoic Xiamaling marine shale in Zhangjiakou,Hebei

The adsorption capacity of high–over-matured shale has been widely investigated, but the adsorption capacity and the main factors influencing low–middle-matured, type II kerogen-containing, and organic-rich marine shale have been rarely explored. This research conducts organic geochemistry, mineralogical composition, adsorption isotherm tests to reveal the adsorption and main influencing factors of the different geochemistry characteristics, mineralogical compositions, temperature and pressure conditions of the low–middle-matured Neoproterozoic Xiamaling marine shale in Zhangjiakou, Hebei. The investigated shale is in a low–middle maturity stage, contains type II kerogen and is rich in organic matter. The results show that the total organic carbon (TOC) content of the Xiamaling shale is positively correlated with the methane adsorption capacity, which is the most important influencing factor on the adsorptive property of shale. The methane adsorption capacity first decreases to the minimum value as the temperature reaches 360°C equivalent Ro (EqRo = 1.0%), then increases and reaches the maximum value at 620°C (EqRo = 3.28%) and finally decreases again as the temperature rises at the last simulation stage. The mineral components exhibit an insignificant influence on the methane absorbability because of organic-matter coatings. The TOC-normalised methane adsorption capacity is positively correlated with the illite–smectite and clay-mineral contents but shows no significant correlation with brittle minerals, such as quartz. Soluble organic matter and kerogen caused the methane dissolution and adsorbtion, respectively. The strong dissolution property of the soluble organic matter is the most important cause of the larger adsorption capacity of the original shale compared with that of the residual samples. Moreover, the methane adsorption capacity of the Xiamaling shale decreases with increasing temperature, and increases with pressure below the critical pressure but decreases exceeding the critical pressure.     

Formation of solid bituminous matter in pegmatites: Constraints from experimentally formed organic matter on microporous silicate minerals

The formation of solid bituminous matter (SBM) on surfaces of microporous silicates was experimentally studied at pressure and temperature conditions typical of late-stage magmatic and hydrothermal processes. Aliquots of microporous silicate minerals (zorite and kuzmenkoite-Mn, Lovozero Alkaline Massif, Kola Peninsula, Russia) were exposed to solid or liquid organic carbon sources (natural brown coal and liquid 1-hexene for synthesis purposes) in a 0.1 M NaCl-solution for 7 days, at constant pressure (50 MPa), and at three individual temperatures (200, 275, and 300 °C). No thermal decomposition of the solid organic sources happened at 200 °C and only a thin film of brown coal derivatives on the silicates’ surfaces and no formation of SBM were observed at 275 °C and 300 °C. But solid bituminous matter on the surfaces of both microporous silicates were detected in experiments with liquid 1-hexene as organic carbon source and at temperatures of 275 °C and 300 °C with a more pronounced formation of SBM at 300 °C compared to 275 °C. The aromatic and aliphatic hydrocarbons, as well as alcoholic compounds of the experimentally produced SBM are similar, if not even partly identical, with natural SBM occurrences of the Khibiny and Lovozero Massifs, Kola Peninsula, Russia, and from the Viitaniemi granitic pegmatite, Finland, as shown by FT-IR and ¹H NMR spectroscopy. This strengthens the hypothesis of formation of natural solid bituminous matter by catalytic reactions between microporous Ti-, Nb- and Zr-silicates and hydrocarbons at postmagmatic hydrothermal conditions.     

沉积盆地热化学硫酸盐还原作用评述

川东天然气藏H2S 气体泄露而导致重大伤亡事故后,热化学硫酸盐还原作用（TSR）成为了国内研究的热点。在油气储层条件下,尽管甲烷是最稳定的烃类,但TSR被诱发后,因为甲烷浓度远高于其它烃类,水溶甲烷能与硫酸根离子反应产生H2S 气体。同时,发现在参与TSR反应的有机质、起始温度、硫同位素分馏效应等方面,实验模拟结果均与地质实例观察结果有较大的差异,可能与TSR反应的催化剂等方面认识不足有关。并认为,TSR成因的H2S或元素硫可以在晚成岩期合并入有机质中,形成新的有机含硫化合物。但在自然界中,这类化合物很少被鉴别出来。     

Abiogenic Origin of Hydrocarbons: An Historical Overview

Abstract. The two theories of abiogenic formation of hydrocarbons, the Russian-Ukrainian theory of deep, abiotic petroleum origins and Thomas Gold's deep gas theory, have been considered in some detail. Whilst the Russian-Ukrainian theory was portrayed as being scientifically rigorous in contrast to the biogenic theory which was thought to be littered with invalid assumptions, this applies only to the formation of the higher hydrocarbons from methane in the upper mantle. In most other aspects, in particular the influence of the oxidation state of the mantle on the abundance of methane, this rigour is lacking especially when judged against modern criteria as opposed to the level of understanding in the 1950s to 1980s when this theory was at its peak. Thomas Gold's theory involves degassing of methane from the mantle and the formation of higher hydrocarbons from methane in the upper layers of the Earth's crust. However, formation of higher hydrocarbons in the upper layers of the Earth's crust occurs only as a result of Fischer-Tropsch-type reactions in the presence of hydrogen gas but is otherwise not possible on thermodynamic grounds. This theory is therefore invalid. Both theories have been overtaken by the increasingly sophisticated understanding of the modes of formation of hydrocarbon deposits in nature.     

Palynomorph stratigraphy,palynofacies and organic geochemistry assessments for hydrocarbon generation of Ratawi Formation,Iraq

Seventy-two core and cutting samples of the Ratawi Formation from selected wells of central and southern Iraq in Mesopotamian Foredeep Basin are analysed for their sedimentary organic matters. Dinoflagellates, spores and pollen are extracted by palynological techniques from these rocks. Accordingly, Hauterivian and late Valanginian ages are suggested for their span of depositional time. These palynomorphs with other organic matter constituents, such as foraminifer’s linings, bacteria and fungi, are used to delineate three palynofacies types that explain organic matter accumulation sites and their ability to generate hydrocarbons. Palaeoenvironments of these sites were mainly suboxic to anoxic with deposition of inshore and neritic marine environments especially for palynofacies type 2. Total organic matters of up to 1.75 total organic carbon (TOC) wt.% and early mature stage of up to 3.7 TAI based on the brown colour of the spore species Cyathidites australis and Gleichenidites senonicus with mottled interconnected amorphous organic matter are used for hydrocarbon generation assessment from this formation. On the other hand, these rock samples are processed with Rock-Eval pyrolysis. Outcomes and data calculations of these analyses are plotted on diagrams of kerogen types and hydrocarbon potential. Theses organic matter have reached the mature stage of up to T _max?=?438 °C, hydrogen index of up to 600 mg hydrocarbons for each gram of TOC wt.% and mainly low TOC (0.50–1.55). Accordingly, this formation could generate fair quantities of hydrocarbons in Baghdad oil field and Basrah oil fields. Organic matters of this formation in the fields of Euphrates subzone extends from Hilla to Nasiriyah cities have not reached mature stage and hence not generated hydrocarbons from the Ratawi Formation. Software 1D PetroMod basin modelling of the Ratawi Formation has confirmed this approach of hydrocarbon generation with 100 % transformations of the intended organic matters to generate hydrocarbons to oil are performed in especially oil fields of East Baghdad, West Qurna and Majnoon while oil fields Ratawi and Subba had performed 80–95 % transformation to oil and hence end oil generation had charged partly the Tertiary traps that formed during the Alpine Orogeny. Oil fields of Nasiriyah and Kifle had performed least transformation ratio of about 10–20 % transformation to oil, and hence, most of the present oil in this field is migrated from eastern side of the Mesopotamian Foredeep Basin that hold higher maturation level.     

Organic geochemistry of the 9.6 km Bertha Rogers No. 1. well,Oklahoma

Organic geochemical analyses of fine-grained rocks from the 9.590 km Bertha Rogers No. 1 well have been carried out: total organic carbon, Soxhlet extraction and silica gel chromatography, C₁₅₊ saturated and aromatic hydrocarbon gas chromatography and mass spectrometry, pyrolysis, kerogen analysis, X-ray diffraction and visual kerogen analysis.Rocks ranged in age from Permian to Ordovician; the well has an estimated bottom hole temperature of 225°C. Some data from this study are inconsistent with conventional theories concerning the generation and thermal destruction of hydrocarbons. For example, appreciable amounts of C₁₅₊ gas-condensate-like hydrocarbons are present in very old rocks currently at temperatures where current theory predicts that only methane and graphite should remain. Also, substantial amounts of pyrolyzable C₁₅₊ hydrocarbons remain on the kerogen in these deeply buried Paleozoic rocks. This suggests, at least in somes cases, that temperatures much higher than those predicted by current theory are required for generation and thermal destruction of hydrocarbons. The data from this well also suggest that original composition of organic matter and environment of deposition may have a much stronger influence on the organic geochemical characteristics of fine-grained sediments than has previously been ascribed to them. The results from this well, from other deep hot wells in which temperatures exceed 200°C, and from laboratory experiments, suggest that some of the basic concepts of the generation and maturation of petroleum hydrocarbons may be in error and perhaps should be reexamined.     

The deep subsurface temperature controlled origin of the gaseous and gasoline-range hydrocarbons of petroleum

In recent surface sediments there is no indication of any of the saturated C₃–C₇ gasolinerange hydrocarbons which are so common in petroleum. Appreciable gasoline-range hydrocarbon generation (85–180°C) of 80 ppm by weight of dry rock, or more, occurs only with increased temperature due to deeper burial, below about 8000 ft in the Los Angeles basin and below 12,500 ft in the Ventura basin. Because of the lower temperature gradient in the Ventura basin, the zone of substantial gasoline generation is considerably deeper there than in the Los Angeles basin. However, the subsurface temperature range over which substantial gasoline generation occurs is practically the same in the two basins. This demonstrates that the subsurface temperature, not depth, is the controlling factor in gasoline generation in source rocks. For appreciable gasoline generation somewhat higher subsurface temperatures are required than for equivalent generation of heavy hydrocarbons boiling above 325°C. Appreciable generation of the C₁–C₄ wet gas components of 75 ppm by weight of dry rock, or more, takes place quite deep also; in the Los Angeles basin it occurs below 10,000 ft.The composition of the gasoline-range hydrocarbons generated changes gradually with increasing depth, temperature and age of the shales. In deep strata the gasolines from shale cannot be distinguished from the gasolines of waxy crude oils in the same basin. The gasoline-range hydrocarbons mature with depth, temperature and age of the sediments, very much like the heavy hydrocarbons investigated earlier.Based on the similarity of analyses of heavy as well as of gasoline-range hydrocarbons from crude oils and from certain deep shales, a secure identification has been made of mature oil source beds in the Los Angeles and San Joaquin Valley oil basins of California. The combined results of these studies provide strong evidence for the origin of petroleum from the organic matter of sediments.     

Pyrite-hydrocarbon Interaction under Hydrothermal Conditions: an Alternative Origin of H2S and Organic Sulfur Compounds in Sedimentary Environments

Sulfate rocks and organic sulfur from sedimentary organic matter are conventionally assumed as the original sulfur sources for hydrogen sulfide(H_2S) in oil and gas reservoirs. However,a few recent experiments preliminarily indicate that the association of pyrite and hydrocarbons may also have implications for H_2S generation,in which water effects and natural controls on the evolution of pyrite sulfur into OSCs and H_2S have not been evaluated. In this study,laboratory experiments were conducted from 200 to 450° C to investigate chemical interactions between pyrite and hydrocarbons under hydrothermal conditions. Based on the experimental results,preliminary mechanism and geochemical implications were tentatively discussed. Results of the experiments showed that decomposition of pyrite produced H_2S and thiophenes at as low as 330°C in the presence of water and n-pentane. High concentrations of H_2S were generated above 450°C under closed pyrolysis conditions no matter whether there is water in the designed experiments. However,much more organic sulfur compounds(OSCs) were formed in the hydrous pyrolysis than in anhydrous pyrolysis. Generally,most of sulfur liberated from pyrite at elevated temperatures was converted to H_2S. Water was beneficial to breakdown of pyrite and to decomposition of alkanes into olefins but not essential to formation of large amounts of H_2S,given the main hydrogen source derived from hydrocarbons. In addition,cracking of pyrite in the presence of 1-octene under hydrous conditions was found to proceed at 200°C,producing thiols and alkyl sulfides. Unsaturated hydrocarbons would be more reactive intermediates involved in the breakdown of pyrite than alkanes. The geochemistry of OSCs is actually controlled by various geochemical factors such as thermal maturity and the carbon chain length of the alkanes. This study indicates that the scale of H_2S gas generated in deep buried carbonate reservoirs via interactions between pyrite and natural gas should be much smaller than that of thermochemical sulfate reduction(TSR) due to the scarcity of pyrite in carbonate reservoirs and the limited amount of long-chained hydrocarbons in natural gas. Nevertheless,in some cases,OSCs and/or low contents of H_2S found in deep buried reservoirs may be associated with the deposited pyrite-bearing rock and organic matters(hydrocarbons),which still needs further investigation.     

Transformation of the pore space during the simulation of the generation of hydrocarbon fluids in the Domanik horizon of the South-Tatar crest as an example

The main purpose of this paper is to study the factors that control changes in rock structure during catagenetic transformation of organic matter. Hydrocarbon generation and primary migration can be controlled by numerous parameters; the most important are temperature, pressure, hydrocarbon composition, and organic matter type and content. The influences of most of these parameters have been studied and experimentally demonstrated. However, there are a few works that are dedicated to the investigation of the texture features of rocks, as well as the quantitative content of the organic matter on the pore space transformation of rocks. Therefore, these parameters are the most important when studying the primary migration processes. It was found experimentally that the rock pore space after each stage of heating is transformed, forming new pore spaces and channels that connect the primary pores. A sample with a relatively low content of organic matter has been found to undergo fewer changes in pore-space morphology in comparison to rock that is saturated in organic content. It has been found that that the change of pore-space morphology depends on the original structure of the rocks. Most of the structural changes were observed during rock heating within 260–430°C; the most intense formation of hydrocarbons was revealed within this interval.     

Evidence for bacterial degradation of hydrocarbons in uranium deposits

The biodegradation of free hydrocarbons migrated in reservoir faaes has often been observed in petroleum exploration. This bacterial alteration is characterized by the progressive removal of different classes of hydrocarbons. One of the most important consequences of biodegradation is the reduction of sulphate, as noted in several Pb-Zn deposits. Biodegradation of oils spatially associated with uranium deposits has also been observed in Lodeve (France), Grand Canyon (Arizona, USA), Temple Mountain (Utah, USA) and leads to the transformation of fluid oils into solid bitumens. Within this study emphasis has been laid on the relationships between the effects of biodegradation on organic matter (oxidation or aromatization) and the nature of aqueous solutions analysed in fluid inclusions trapped in authigenic minerals. Different mechanisms are proposed to explain the transformations of organic matter during biodegradation and their possible links with ore-forming processes.     

有机质演化与沉积矿床成因(Ⅱ)--煤成烃类与层控矿床

成煤物质被埋藏以后,在其煤化作用过程中可生成大量气体烃(即煤成气)与少量液体烃(即煤成油)。按照B. JI.科兹洛夫计算值一吨煤产生的甲烷量，褐煤阶段为68M3，到焦煤达270M3，到无烟煤可超过400M3     

Coal weathering and the geochemical carbon cycle

The weathering rate of sedimentary organic matter in the continental surficial environment is poorly constrained despite its importance to the geochemical carbon cycle. During this weathering, complete oxidation to carbon dioxide is normally assumed, but there is little proof that this actually occurs. Knowledge of the rate and mechanisms of sedimentary organic matter weathering is important because it is one of the major controls on atmospheric oxygen level through geologic time.We have determined the aqueous oxidation rates of pyrite-free bituminous coal at 24° and 50°C by using a dual-cell flow-through method. Coal was used as an example of sedimentary organic matter because of the difficulty in obtaining pyrite-free kerogen for laboratory study. The aqueous oxidation rate obtained in the present study for air-saturated water (270 μM O₂) was found to be on the order of 2 × 10⁻¹² mol O₂/m²/s at 25°C, which is fast compared to other geologic processes such as tectonic uplift and exposure through erosion. The reaction order with respect to oxygen level is 0.5 on a several thousand hour time scale for both 24° and 50°C experiments. Activation energies, determined under 24° and 50°C conditions, were ≈40 kJ/mol O₂ indicating that the oxidation reaction is surface reaction controlled.The oxygen consumption rate obtained in this study is two to three orders of magnitude smaller than that for pyrite oxidation in water, but still rapid on a geologic time scale. Aqueous coal oxidation results in the formation of dissolved CO₂, dissolved organic carbon (DOC), and solid oxidation products, which are all quantitatively significant reaction products.     

Chromatographic study of formation conditions of rhombododecahedral diamond crystals

The results of chromatographic study of the formation of rhombododecahedral diamonds synthesized in the Fe-Ni-(Ti)-C system at 5.5–6.0 GPa and 1350–1450°C are presented, including crystals with rounded surfaces of the rhombododecahedron with parallel striation, which are morphological analogues of natural diamonds abundant at various kimberlite, lamproite, and placer deposits. Chromatography was performed at 150°C with mechanical breakup of diamonds. The stable release of methane when diamonds of habit {110} are crushed is established. It is concluded that the appearance of the habit rhombododecahedron may be related not only to the effect of temperature and pressure on crystal growth but also to reductive conditions of crystallization. At the same time, the appearance of significant amounts of hydrocarbons in the system probably results in stopping of the growth of faces {110} and {100} and, instead, formation of specific surfaces that are composed of microscopic accessories faced by planes {111}.     

Kerogen of Toarcian shales of the Paris Basin. A study of its maturation by flash pyrolysis techniques

A set of 14 samples—both extracted and unextracted from the Toarcian of the Paris Basin have been investigated using Curie-point pyrolysis-mass spectrometry and Curie-point pyrolysis gas chromatography mass spectrometry. The relative amount of n-alkenes and n-alkanes in the pyrolyzates increases with increasing maximum burial depth of the samples. Comparison of the pyrolysis data of extracted and unextracted samples shows that generation of hydrocarbons from the kerogen starts at a maximum burial depth of ~ 1000m. The increase of pristane and phytane in the extracts of the deeper samples is correlated with the gradual decrease of the characteristic pyrolysis product prist-1-ene. Three samples yield pyrolyzates with high relative amounts of aromatic compounds. This phenomenon probably reflects a different type of contributing organic matter and/or a different environment of sedimentation.     

Variscan and post-Variscan lead–zinc mineralization, Rhenish Massif, Germany: evidence for sulfide precipitation via thermochemical sulfate reduction

A mechanical decrepitation device coupled with a gas chromatograph has been used to characterize the molecular composition of gaseous and liquid hydrocarbons contained in minerals. Application of this technique allows the identification of low-molecular-weight n-alkanes and some aromatic hydrocarbons in sulfides and gangue minerals from epigenetic Variscan and post-Variscan lead–zinc deposits in the Rhenish Massif, Germany. Based on the analysis of 200 samples, Variscan and post-Variscan mineralization can be distinguished by the composition of associated hydrocarbons. Variscan sulfides and gangue minerals contain high abundancies of methane. In contrast, n-alkanes in the C₂–C₉ range and aromatic hydrocarbons (benzene, toluene) are dominant in post-Variscan mineralization. The absence of high-molecular-weight hydrocarbons in ore minerals suggests highly mature gas associated with hydrothermal activity, during which hydrothermal fluids caused an increase in thermal maturation of organic matter and the generation of low-molecular-weight hydrocarbons in the adjacent organic-rich rocks. The hydrocarbon compositions contained in fluid inclusions of Variscan and post-Variscan minerals are probably governed by the maturation level of the potential source rocks. In Variscan time tectonic brines (T > 175 °C) generated predominantly methane, whereas basement brines (T < 175 °C) expelled higher-molecular-weight hydrocarbons (wet gases, condensates, aromatic hydrocarbons) from adjacent rocks during the Mesozoic event. The specific role of hydrocarbons in sulfide precipitation via thermochemical sulfate reduction is indicated by geochemical characteristics of organic matter associated with the Plombières Pb–Zn deposit, in eastern Belgium. Intense alteration phenomena were observed in near-ore kerogens, compared with unaltered kerogens far from the ore body, as well as by a very high maturity (5.40% R_o), a systematic depletion in ¹²C towards the vein-type mineralization, high atomic S/C ratios (0.49), and by low atomic H/C ratios (0.29). The data suggest that hydrothermal solutions caused a drastic increase in the thermal maturation of organic matter within the adjacent wall rock. Increased thermal maturation resulted in increased δ¹³C-values of organic carbon due to the preferential release of ¹²C. The change in the organic matter to a H-depleted and S-enriched bulk composition in association with sulfide ores strongly suggests that thermochemical sulfate reduction was responsible for organic degradation. Thus, thermochemical sulfate reduction probably triggered base metal sulfide precipitation in Variscan and post-Variscan ore deposits of the Rhenish Massif. Finally, based on data from this study and previous investigations, new genetic models are presented for both Variscan and post-Variscan mineralization in the Rhenish Massif. Received: 15 September 1999 / Accepted: 2 December 1999     

A Study on Organic Inclusions in Clastic Reservoir Rocks and Their Application to the Assessment of Oil and Gas Accumulations

Terrigenous clastic reservoir rocks are widespread in China,and nearly all the industrial oil and gas accumulations in eastern China occur in the clastic rocks.The study shows that organic inclusions are mostly distributed in the secondary fissures and pores which were ormed in the process of oil-rock interaction,rather than in the cements or secondary enlargements. The organic inclusions are dominantly organic gas-rich or are composed of pure hydrocarbons.Homogenization temperatures range mainly from 120℃ to 130℃，which shows a relatively high maturity of organic matter.Vertical and horizontal temperature changes provide the grounds for the investigation of basin evolution and thermal fluid-kinetics-model.Fluorescence spectral characteristics o the organic inclusions indicate that oils and gases in the area studied probably have experienced two-stage or two-time migration.Micro-fluorescence rescearch is one of the effective approaches to oil/source correlation and oil migration-stage determination.The abundance and occurrence of organic inclusions is one of the indicators of oil and gas abundance and accumulation in rock layers.With the help of other informatio,organic inclusions can provide the basis for the prospective assessment of oil and gas in clastic reservoir rocks.     

High H2S contents and other effects of thermochemical sulfate reduction in deeply buried carbonate reservoirs: a review

The accumulation of high H₂S concentrations in oil and gas fields is usually associated with deeply buried high-temperature carbonate reservoirs and is attributed to the abiological oxidation of hydrocarbons by sulfate – thermochemical sulfate reduction (TSR). This review aims at providing an overview of the literature and assessing existing uncertainties in the current understanding of TSR processes and their geological significance. Reaction pathways, various reaction products, the autocatalytic nature of TSR, and reaction kinetics are discussed. Furthermore, various criteria for recognizing TSR effects, such as petrographic/diagenetic alterations and stable isotope geochemistry of the inorganic as well as the organic reactants, are summarized and evaluated. There is overwhelming geological evidence of TSR taking place at a minimum temperature of 110–140?°C, but the temperature discrepancy between experimental data and nature still exists. However, the exact nature and mechanisms of catalysts which influence TSR are not known. Local H₂S variations may reflect steady-state conditions dominated by H₂S buildups and flux out of the system. The latter is controlled by lithological and geological factors.