Geochemical features and origin of natural gas in heavy oil area of the Western Slope,Songliao Basin,China

The Western Slope of the Songliao Basin is rich in heavy oil resources (>70 × 10⁸ bbl), around which there are shallow gas reservoirs (∼1.0 × 10¹² m³). The gas is dominated by methane with a dryness over 0.99, and the non-hydrocarbon component being overwelmingly nitrogen. Carbon isotope composition of methane and its homologs is depleted in ¹³C, with δ¹³C₁ values being in the range of −55‰ to −75‰, δ¹³C₂ being in the range of −40‰ to −53‰ and δ¹³C₃ being in the range of −30‰ to −42‰, respectively. These values differ significantly from those solution gases source in the Daqing oilfield. This study concludes that heavy oils along the Western Slope were derived from mature source rocks in the Qijia-Gulong Depression, that were biodegraded. The low reservoir temperature (30–50 °C) and low salinity of formation water with neutral to alkaline pH (NaHCO₃) appeared ideal for microbial activity and thus biodegradation. Natural gas along the Western Slope appears mainly to have originated from biodegradation and the formation of heavy oil. This origin is suggested by the heavy δ¹³C of CO₂ (−18.78‰ to 0.95‰) which suggests that the methane was produced via fermentation as the terminal decomposition stage of the oil.     

Geochemical characterization of secondary microbial gas occurrence in the Songliao Basin, NE China

A suite of natural gases from the northern Songliao Basin in NE China were characterized for their molecular and carbon isotopic composition. Gases from shallow reservoirs display clear geochemical evidence of alteration by biodegradation, with very high dryness (C₁/C₂₊ > 100), high C₂/C₃ and i-C₄/n-C₄ ratios, high nitrogen content and variable carbon dioxide content. Isotopic values show wide range variations (δ¹³C_CH4 from −79.5‰ to −45.0‰, δ¹³C_C2H6 from −53.7‰ to −32.2‰, δ¹³C_C3H8 from −36.5‰ to −20.1‰, δ¹³C_nC4H10 from −32.7‰ to −24.5‰, and δ¹³C_CO2 from −21.6‰ to +10.5‰). A variety of genetic types can be recognized on the basis of chemical and isotopic composition together with their geological occurrence. Secondary microbial gas generation was masked by primary microbial gas and the mixing of newly generated methane with thermogenic methane already in place in the reservoir can cause very complicated isotopic signatures. System openness also was considered for shallow biodegraded gas accumulations. Gases from the Daqing Anticline are relatively wet with ¹³C enriched methane and ¹³C depleted CO₂, representing typically thermogenic origin. Gases within the Longhupao-Da’an Terrace have variable dryness, ¹³C enriched methane and variable δ¹³C of CO₂, suggesting dominant thermogenic origin and minor secondary microbial methane augment. The Puqian-Ao’nan Uplift contains relatively dry gas with ¹³C depleted methane and ¹³C enriched CO₂, typical for secondary microbial gas with a minor part of thermogenic methane. Gas accumulations in the Western Slope are very dry with low carbon dioxide concentrations. Some gases contain ¹³C depleted methane, ethane and propane, indicating low maturity/primary microbial origin. Recognition of varying genetic gas types in the Songliao Basin helps explain the observed dominance of gas in the shallow reservoir and could serve as an analogue for other similar shallow gas systems.     

Evidence for deep anaerobic biodegradation associated with rapid sedimentation and burial in the Beaufort–Mackenzie basin,Canada

Formation waters of the 14 km thick late Cretaceous–Cenozoic Beaufort–Mackenzie basin were examined as part of a larger project to better understand the petroleum potential of the region, where early exploration defined petroleum reserves of 744 × 10⁹ bbls recoverable crude oil and 11.74 tcf gas. Historical water analyses (2583 samples from 250 wells drilled up to 5 km depth) were compiled and culled to remove incomplete and poor quality samples. The resultant database shows a broad range of salinity and water chemistry that has no systematic relationship with depth. Three main water types are defined, paleo seawater, and freshwaters related to a Miocene age gravity-driven flow system, and low TDS–high alkalinity waters. High alkalinity waters are isolated in overpressured fault blocks that were rapidly buried by post-Miocene Iperk shale deposition. The high alkalinities (up to 9000 mg/L) are interpreted to be related to in situ CO₂ generation through anaerobic methanogenesis in response to freshwater invasion. The dominant control on biogenic gas generation appears to be maximum burial temperature rather than the modern temperature distribution. This is consistent with the paleopasteurization model that suggests once critical burial temperatures are reached, sterilized rocks are inhibited from further biodegradation, even when temperatures subsequently drop back into the habitable zone.     

A geochemical study on mud volcanoes in the Junggar Basin, China

A comprehensive study was performed to characterize, for the first time, the mud, water, and gases released from onshore mud volcanoes located in the southern margin of the Junggar Basin, northwestern China. Chemical compositions of mud, along with the geology of the basin, suggest that a source of the mud is Mesozoic or Cenozoic shale. Oxygen and H isotope compositions of the released water suggest a local meteoric origin. Combined with the positive Eu anomalies of the water, a large ¹⁸O shift of the water suggests extensive interaction with rocks. Gases discharged from the mud volcanoes are predominantly thermogenic hydrocarbons, and the high δ¹³C values (>+20‰ VPDB) for CO₂ gases and dissolved carbonate in muddy water suggest secondary methanogenesis with CO₂ reduction after oil biodegradation.The enrichments of Eu and ¹⁸O in water and the low thermal gradient of the area suggest that the water-rock interactions possibly occur deeper than 3670 ± 200 m. On the other hand, considering the relationship to the petroleum reservoir around the mud volcanoes, the depth of the gases can be derived from about 3600 m, a depth that is greater than that generally estimated for reservoirs whose gas is characterized by ¹³C-enriched CO₂. Oil biodegradation with CO₂ reduction likely occurs at a shallower depth along the seepage system of the mud volcano. The results contribute to the worldwide data set of gas genesis in mud volcanoes. Moreover, they further support the concept that most terrestrial mud volcanoes release thermogenic gas produced in very deep sediments and may be early indicators of oil biodegradation, an important problem in the petroleum industry.     

根据储层沥青和流体包裹体综合判识油气成藏期:以黄骅坳陷北大港古生界潜山为例

渤海湾盆地潜山油气资源较丰富,近期黄骅坳陷古生界潜山油气勘探取得重大进展,但油气藏的形成时期及期次尚不明确.以黄骅坳陷北大港古生界潜山为例,综合利用储层沥青、流体包裹体观察、测温、拉曼光谱及红外光谱分析等地球化学分析手段,结合烃源岩生烃史,对其油气成藏期进行了系统研究.结果表明:研究区古生界发育碳质、胶质-沥青质、油质3种沥青,经历了生物降解和氧化作用等多种次生改造过程,结合研究区的构造演化及生烃史,推测早侏罗世中期之前存在油气充注;古生界潜山发育两期烃类包裹体,第一期包裹体发黄褐色荧光,主要分布于石英颗粒表面及方解石脉内,均一温度峰值区间为75~80℃,第二期包裹体包括黄色、蓝绿色荧光两类,分布在石英颗粒内裂缝、穿石英颗粒裂缝及方解石脉内,均一温度峰值范围分别为85~90℃和95~100℃;综合古生界潜山储层沥青及包裹体特征,结合烃源岩生烃史,确定古生界存在两期油气充注,分别为中三叠世（235~223 Ma）和新近纪-第四纪（22~0 Ma）,且以晚期成藏为主.      

Methane microseepage from different sectors of the Yakela condensed gas field in Tarim Basin,Xinjiang, China

Methane microseepage is the result of natural gas migration from subsurface hydrocarbon accumulations to the Earth’s surface, and it is quite common in commercial petroleum fields. While the role of microseepage as a pathfinder in petroleum exploration has been known for about 80 a, its significance as an atmospheric CH₄ source has only recently been studied, and flux data are currently available only in the USA and Europe. With the aim of increasing the global data-set and better understanding flux magnitudes and variabilities, microseepage is now being extensively studied in China. A static flux chamber method was recently applied to study microseepage emissions into the atmosphere in four different sectors of the Yakela condensed gas field in Tarim Basin, Xinjiang, China, and specifically in: (a) a faulted sector, across the Luntai fault systems; (b) an oil–water interface sector, at the northern margin of the field; (c) an oil–gas interface sector, in the middle of the field; (d) an external area, outside the northern gas field boundaries. The results show that positive CH₄ fluxes are pervasive in all sectors and therefore, only part of the CH₄ migrating from the deep oil–gas reservoirs is consumed in the soil by methanotrophic oxidation. The intensity of gas seepage seems to be controlled by subsurface geologic settings and lateral variabilities of natural gas pressure in the condensed gas field. The highest CH₄ fluxes, up to ∼14 mg m⁻² d⁻¹ (mean of 7.55 mg m⁻² d⁻¹) with higher spatial variability (standard deviation, σ: 2.58 mg m⁻² d⁻¹), occur in the Luntai fault sector. Merhane flux was lower in the oil–water area (mean of 0.53 mg m⁻² d⁻¹) and the external area (mean of 1.55 mg m⁻² d⁻¹), and at the intermediate level in the gas–oil sector (mean of 2.89 mg m⁻² d⁻¹). These values are consistent with microseepage data reported for petroleum basins in the USA and Europe. The build-up of methane concentration in the flux chambers is always coupled with an enrichment of ¹³C, from δ¹³C₁ of −46‰ to −42.5‰ (VPDB), which demonstrates that seeping methane is thermogenic, as that occurring in the deep Yakela reservoir. Daily variations of microseepage are very low, with minima in the afternoon, corresponding to higher soil temperature (and higher methanotrophic consumption), and maxima in the early morning (when soil temperatures are lowest). A preliminary and rough estimate of the total amount of CH₄ exhaled from the Yakela field is in the order of 10² tonnes a⁻¹.     

新疆三塘湖盆地马朗凹陷石炭系原油形成过程及勘探意义

新疆三塘湖盆地马朗凹陷牛圈湖构造带马25井石炭系火山岩储层中发现了原油和固体沥青共存,通过储层多级分离抽提和原油地球化学分析,并对这些原油(或固体沥青)的形成过程与其勘探意义进行了研究,结果表明这些原油和沥青可能主要来自下石炭统烃源岩,具有较低姥植比和伽玛蜡烷含量、高丰度三环萜、高Ts/Tm比值和重族组分碳同位素(δ13C-28.0‰)特征;现今油藏原油富含生物降解标志物(25-降藿烷),同时却无明显其它生物降解特征(正构烷烃、甾藿烷等保存完整),反映多期充注特征,即二叠纪中晚期成藏后遭受生物降解,白垩纪后期又再次充注形成;下石炭系有效烃源岩的存在预示着本区具有深部下石炭统源岩贡献的油气藏勘探前景。     

试论渤海湾盆地油气富集规律与勘探

渤海湾盆地至今已发现油气田226个,探明油气地质储量114.4×108t,油气资源量为285×108t。盆地内的油气富集规律与盆地东界的郯庐深大断裂带紧密相关。靠近郯庐断裂带的东部坳陷区,其探明油气地质储量和油气资源量是远离断裂带的西部坳陷区的3.6倍和3.3倍;根据探明油气地质储量进行划分,东部坳陷区以大油气田为主,而西部坳陷区则以中、小油气田为主;东部坳陷区发现的浅层油气藏、稠油油藏、火成岩油藏及非烃CO2气藏比西部坳陷区多得多,但两者的潜山油气藏的数量和储量却很相近。研究表明,郯庐深大断裂不仅控制了盆地的发育和形成,而且还控制了油气的生成、运移和聚集。渤海湾盆地既是中国大盆地中油气富集程度最高的盆地,也是具有独特油气富集规律的盆地。尽管该盆地油气探明率已达40.1%,但仍有170.7×108t的油气剩余资源量可供再勘探,勘探潜力仍十分巨大。     

Deciphering biodegradation effects on light hydrocarbons in crude oils using their stable carbon isotopic composition: A case study from the Gullfaks oil field, offshore Norway

Compound-specific isotope analysis has become an important tool in environmental studies and is an especially powerful way to evaluate biodegradation of hydrocarbons. Here, carbon isotope ratios of light hydrocarbons were used to characterise in-reservoir biodegradation in the Gullfaks oil field, offshore Norway. Increasing biodegradation, as characterised, for example, by increasing concentration ratios of Pr/n-C₁₇ and Ph/n-C₁₈, and decreasing concentrations of individual light hydrocarbons were correlated to ¹³C-enrichment of the light hydrocarbons. The δ¹³C values of C₄ to C₉n-alkanes increase by 7-3‰ within the six oil samples from the Brent Group of the Gullfaks oil field, slight changes (1-3‰) being observed for several branched alkanes and benzene, whereas no change (<1‰) in δ¹³C occurs for cyclohexane, methylcyclohexane, and toluene. Application of the Rayleigh equation demonstrated high to fair correlation of concentration and isotope data of i- and n-pentane, n-hexane, and n-heptane, documenting that biodegradation in reservoirs can be described by the Rayleigh model. Using the appropriate isotope fractionation factor of n-hexane, derived from laboratory experiments, quantification of the loss of this petroleum constituent due to biodegradation is possible. Toluene, which is known to be highly susceptible to biodegradation, is not degraded within the Gullfaks oil field, implying that the local microbial community exhibits rather pronounced substrate specificities. The evaluation of combined molecular and isotopic data expands our understanding of the anaerobic degradation processes within this oil field and provides insight into the degradative capabilities of the microorganisms. Additionally, isotope analysis of unbiodegraded to slightly biodegraded crude oils from several oil fields surrounding Gullfaks illustrates the heterogeneity in isotopic composition of the light hydrocarbons due to source effects. This indicates that both source and also maturity effects have to be well constrained when using compound-specific isotope analysis for the assessment of biodegradation.     

Use of comprehensive two-dimensional gas chromatography/time-of-flight mass spectrometry for the characterization of biodegradation and unresolved complex mixtures in petroleum

A comprehensive two-dimensional gas chromatography/time-of-flight mass spectrometry (GC × GC/TOFMS) method has been developed for separation of a series of petroleum samples using a polar/non-polar column set configuration. Groups of oils were selected to provide samples from the same oil family to assist in comparison of compositional changes during biodegradation. The groups also represented different sources and ages to allow an assessment of the application of GC × GC for the differentiation of oil source, as well as fluid history. The increased resolution and separation afforded by the GC × GC technique provides more complete compositional information on complex biodegraded oil samples than one-dimensional GC, and improves the ability to study biodegradation trends. Among the components identified, it is proposed that alkyl-decahydronaphthalenes constitute a significant contribution to the UCM.     

中国非常规油气勘探与研究新进展

全球油气勘探目标的转移和石油地质学的发展,具有从毫-微米孔喉的圈闭油气,逐渐向纳米孔喉的连续型油气聚集发展的趋势。近十年非常规油气资源在全球能源格局中的地位愈发重要,致密气、煤层气、重油、沥青砂等已成为勘探开发的重点领域,致密油成为亮点领域,页岩气成为热点领域。中国致密气、页岩气、致密油、煤层气等非常规油气资源勘探开发取得重要突破,油页岩、天然气水合物、油砂矿等有重要进展。中国非常规油气研究也取得重大进展,陆相敞流湖盆大型浅水三角洲砂体、湖盆中心砂质碎屑流沉积和湖相碳酸盐岩等,提供了湖盆中心储集体形成和分布的理论依据;创新发展了连续型油气聚集理念,明晰了连续型油气聚集的10个基本地质特征和2项关键标志,为大面积非常规油气规模勘探开发奠定了理论基础;系统表征了致密油气储层的纳米级微观孔喉结构,首次发现了纳米孔喉中油气的赋存,推动了纳米孔喉中油气流动机制和分布规律的研究。随着全球石油工业和纳米等技术的快速发展,提出了"纳米油气"概念,并指出这是未来石油工业的发展方向,需要发展纳米油气透视观测镜、纳米油气驱替剂、纳米油气开采机器人等换代技术,油气智能化时代即将到来。     

Evaluating transition-metal catalysis in gas generation from the Permian Kupferschiefer by hydrous pyrolysis

Transition metals in source rocks have been advocated as catalysts in determining extent, composition, and timing of natural gas generation (Mango, F. D. (1996) Transition metal catalysis in the generation of natural gas. Org. Geochem.24, 977-984). This controversial hypothesis may have important implications concerning gas generation in unconventional shale-gas accumulations. Although experiments have been conducted to test the metal-catalysis hypothesis, their approach and results remain equivocal in evaluating natural assemblages of transition metals and organic matter in shale. The Permian Kupferschiefer of Poland offers an excellent opportunity to test the hypothesis with immature to marginally mature shale rich in both transition metals and organic matter. Twelve subsurface samples containing similar Type-II kerogen with different amounts and types of transition metals were subjected to hydrous pyrolysis at 330° and 355 °C for 72 h. The gases generated in these experiments were quantitatively collected and analyzed for molecular composition and stable isotopes. Expelled immiscible oils, reacted waters, and spent rock were also quantitatively collected. The results show that transition metals have no effect on methane yields or enrichment. δ¹³C values of generated methane, ethane, propane and butanes show no systematic changes with increasing transition metals. The potential for transition metals to enhance gas generation and oil cracking was examined by looking at the ratio of the generated hydrocarbon gases to generated expelled immiscible oil (i.e., GOR), which showed no systematic change with increasing transition metals. Assuming maximum yields at 355 °C for 72 h and first-order reaction rates, pseudo-rate constants for methane generation at 330 °C were calculated. These rate constants showed no increase with increasing transition metals. The lack of a significant catalytic effect of transition metals on the extent, composition, and timing of natural gas generation in these experiments is attributed to the metals not occurring in the proper form or the poisoning of potential catalytic microcosms by polar-rich bitumen, which impregnates the rock matrix during the early stages of petroleum formation.     

Origin of the Neogene shallow gas accumulations in the Jiyang Superdepression, Bohai Bay Basin

Natural gas resources occur extensively along the east coast of China, with a number of large and medium-sized gas fields being discovered in recent years. Gas reservoirs include Neogene, Paleogene and the underlying Mesozoic and Paleozoic basement. Of the total proven natural gas reserves in the Jiyang Superdepression, Bohai Bay Basin, almost 89.7% is present in the shallow Neogene gas pools, in traps formed on top of the paleotopographic highs and along the margin of the secondary depressions. These gases are closely associated with heavy oils, occurring as gas caps or associated gases within the heavy oil pools, or in separate gas pools above, or updip from, the heavy oil pools. The gases contain over 95% methane and small quantities of alkanes, nitrogen and carbon dioxide. The stable carbon isotopes of methane in these gases are up to 10‰ more positive than those of the thermogenic gases in the deep Paleogene reservoirs, with propane more enriched in ¹³C than butane. This study demonstrated that the majority of the petroleum source rocks in the Jiyang Superdepression tend to be oil-prone, and are currently within or shallower than the conventional oil window (0.45–1.0% Ro). The chemical and carbon isotopic compositions of the gases, together with the moderate to severe biodegradation of the associated heavy oils in the shallow Neogene strata, clearly suggest that the formation of the shallow natural gases in the Jiyang Superdepression result from the anaerobic degradation of accumulated oils in reservoir.     

Carbon and hydrogen isotope fractionation associated with the aerobic microbial oxidation of methane, ethane, propane and butane

Carbon isotope fractionation factors associated with the aerobic consumption of methane (C1), ethane (C2), propane (C3), and n-butane (C4) were determined from incubations of marine sediment collected from the Coal Oil Point hydrocarbon seep field, located offshore Santa Barbara, CA. Hydrogen isotope fractionation factors for C1, C2 and C3 were determined concurrently. Fresh sediment samples from two seep areas were each slurried with sea water and treated with C1, C2, C3 or C4, or with mixtures of all four gases. Triplicate samples were incubated aerobically at 15 °C, and the stable isotope composition and headspace levels of C1-C4 were monitored over the course of the experiment. Oxidation was observed for all C1-C4 gases, with an apparent preference for C3 and C4 over C1 and C2 in the mixed-gas treatments. Fractionation factors were calculated using a Rayleigh model by comparing the δ¹³C and δD of the residual C1-C4 gases to their headspace levels. Carbon isotope fractionation factors (reported in ε or (α-1) × 1000 notation) were consistent between seep areas and were −26.5‰ ± 3.9 for C1, −8.0‰ ± 1.7 for C2, −4.8‰ ± 0.9 for C3 and −2.9‰ ± 0.9 for C4. Fractionation factors determined from mixed gas incubations were similar to those determined from individual gas incubations, though greater variability was observed during C1 consumption. In the case of C1 and C3 consumption, carbon isotope fractionation appears to decrease as substrate becomes limiting. Hydrogen isotope fractionation factors determined from the two seep areas differed for C1 oxidation but were similar for C2 and C3. Hydrogen isotope fractionation factors ranged from −319.9‰ to −156.4‰ for C1 incubations, and averaged −61.9‰ ± 8.3 for C2 incubations and −15.1‰ ± 1.9 for C3 incubations. The fractionation factors presented here may be applied to estimate the extent of C1-C4 oxidation in natural gas samples, and should prove useful in further studying the microbial oxidation of these compounds in the natural environment.     

Water drives the deuterium content of the methane emitted from plants

The spatial distribution of the deuterium content of precipitation has a well-established latitudinal variation that is reflected in organic molecules in plants growing at different locations. Some laboratory and field studies have already shown that the deuterium content of methane emitted from methanogens can be partially related to δD variations of the water in the surrounding environment. Here we present a similar relation for the methane emitted from plant biomass under UV radiation. To show this relation, we determined the hydrogen isotopic composition of methane released from leaves of a range of plants grown with water of different deuterium content (δD = −130‰ to +115‰). The plant leaves were irradiated with UV light and the CH₄ isotopic composition was measured by continuous flow isotope ratio mass spectrometry (CF-IRMS). Furthermore, the deuterium content of bulk biomass and of the methoxyl (OCH₃) groups of the biomass was measured. The D/H ratio successively decreases from bulk biomass (δD = −106‰ to −50‰) via methoxyl groups (δD = −310‰ to −115‰) to the CH₄ emitted (δD = −581‰ to −196‰). The range of isotope ratios in bulk biomass and OCH₃ groups is smaller than in the water used to grow the plants. Methoxyl groups, which contain only non-exchangeable hydrogen, can be used to assess the fraction of external water that was incorporated before OCH₃ groups were formed. Surprisingly, the CH₄ formed under UV irradiation has a wider isotopic range than the OCH₃ groups. Although the precise production pathway cannot be fully determined, the presented experiments indicate that methoxyl groups are not the only source substrate for CH₄, but that other sources, including very depleted ones, must contribute. The main limitation to the interpretation of the data is the possible influence of exchangeable water, which could not be quantified. Future studies should include measurements of leaf water and avoid interaction between different plants via the gas phase. Despite these deficiencies, the results suggest that the deuterium content of the methane generated from plants under UV irradiation is closely linked to δD in precipitation. This dependency, which should also exist for other biogenic methane sources could be evaluated with global isotope models.     

Stable isotopic evidence in support of active microbial methane cycling in low-temperature diffuse flow vents at 9°50′N East Pacific Rise

A unique dataset from paired low- and high-temperature vents at 9°50′N East Pacific Rise provides insight into the microbiological activity in low-temperature diffuse fluids. The stable carbon isotopic composition of CH₄ and CO₂ in 9°50′N hydrothermal fluids indicates microbial methane production, perhaps coupled with microbial methane consumption. Diffuse fluids are depleted in ¹³C by ∼10‰ in values of δ¹³C of CH₄, and by ∼0.55‰ in values of δ¹³C of CO₂, relative to the values of the high-temperature source fluid (δ¹³C of CH₄ =−20.1 ± 1.2‰, δ¹³C of CO₂ =−4.08 ± 0.15‰). Mixing of seawater or thermogenic sources cannot account for the depletions in ¹³C of both CH₄ and CO₂ at diffuse vents relative to adjacent high-temperature vents. The substrate utilization and ¹³C fractionation associated with the microbiological processes of methanogenesis and methane oxidation can explain observed steady-state CH₄ and CO₂ concentrations and carbon isotopic compositions. A mass-isotope numerical box model of these paired vent systems is consistent with the hypothesis that microbial methane cycling is active at diffuse vents at 9°50′N. The detectable ¹³C modification of fluid geochemistry by microbial metabolisms may provide a useful tool for detecting active methanogenesis.     

Role of water in hydrocarbon generation from Type-I kerogen in Mahogany oil shale of the Green River Formation

Hydrous and anhydrous closed-system pyrolysis experiments were conducted on a sample of Mahogany oil shale (Eocene Green River Formation) containing Type-I kerogen to determine whether the role of water had the same effect on petroleum generation as reported for Type-II kerogen in the Woodford Shale. The experiments were conducted at 330 and 350 °C for 72 h to determine the effects of water during kerogen decomposition to polar-rich bitumen and subsequent bitumen decomposition to hydrocarbon-rich oil. The results showed that the role of water was more significant in bitumen decomposition to oil at 350 °C than in kerogen decomposition to bitumen at 330 °C. At 350 °C, the hydrous experiment generated 29% more total hydrocarbon product and 33% more C₁₅₊ hydrocarbons than the anhydrous experiment. This is attributed to water dissolved in the bitumen serving as a source of hydrogen to enhance thermal cracking and facilitate the expulsion of immiscible oil. In the absence of water, cross linking is enhanced in the confines of the rock, resulting in formation of pyrobitumen and molecular hydrogen. These differences are also reflected in the color and texture of the recovered rock. Despite confining liquid-water pressure being 7-9 times greater in the hydrous experiments than the confining vapor pressure in the anhydrous experiments, recovered rock from the former had a lighter color and expansion fractures parallel to the bedding fabric of the rock. The absence of these open tensile fractures in the recovered rock from the anhydrous experiments indicates that water promotes net-volume increase reactions like thermal cracking over net-volume decrease reactions like cross linking, which results in pyrobitumen. The results indicate the role of water in hydrocarbon and petroleum formation from Type-I kerogen is significant, as reported for Type-II kerogen.     

柴东石炭系天然沥青特征及形成的主控因素

前人在柴达木盆地东部石炭系地层中发现了大量的天然沥青出露,并证实柴达木盆地石炭系烃源岩有过生烃过程。因此,深入开展该地区天然沥青特征和形成模式分析,对该地区下一步的油气勘探有着重要的指导意义。文中采用物理和地球化学实验的方法,研究了石炭系天然沥青物理特征和地球化学特征;分析了石炭系天然沥青物理特征和地球化学特征,并总结出石炭系沥青遭受了轻微的生物降解和氧化作用的蚀变特性;通过对沥青形成的地质背景及构造活动的分析和研究,探究了德令哈坳陷沥青的形成模式,发现该区石炭系、侏罗系广泛分布的烃源岩是沥青形成的物质基础;局部的优质储层,为有利的油气储集空间;不整合面和断裂体系非常发育,不仅对该区油气的运移起着控制作用,也是油气藏破坏而暴露地表形成沥青的重要因素;这三个主控因素对该区天然沥青的形成起着决定性的作用     

Biodegradation preference for isomers of alkylated naphthalenes and benzothiophenes in marine sediment contaminated with crude oil

Contamination of coastal marine sediments with polycyclic aromatic hydrocarbons is pervasive, with major sources including anthropogenic activity and natural seepage. Biodegradation serves as a major hydrocarbon sink with evaporation and dissolution responsible for the removal of low boiling range compounds and photo-oxidation acting on many multi-substituted aromatic compounds. In this work, first-order rate constants for aerobic biodegradation were quantified for naphthalene (N), benzothiophene (BT) and their alkylated congeners (1-4 carbon substituents (C1-C4)) in laboratory experiments with oil laden marine sediments from a natural seep. Rate constants were used as proxies for microbial preference, which follows the order: naphthalene > C1N > C2N > C1BT > C2BT > benzothiophene > C3BT > C3N > C4BT > C4N, with some overlap. The application of comprehensive two dimensional gas chromatography further enabled separation and quantification of multiple structural isomers for C2N-C4N and C2BT-C4BT, with 7-12 isomers resolved for each C2N-C4N and 4-7 isomers resolved for each C2BT-C4BT. A strong isomeric biodegradation preference was noted within each of these compound classes, with rate constants varying as much as a factor of 2 for structural isomers of the same compound class. Each isomer was consumed to a low, but non-zero concentration, suggesting that their residual load in sediment may be proportional to the number of structural isomers originally present, in addition to the pattern and the number of alkyl substitutions. The simultaneous first-order biodegradation rates observed for 52 aromatic hydrocarbons resolved in this study, along with reference compounds such as n-alkanes, lends support to the concept of broad scale metabolic specificity during aerobic biodegradation of petroleum.     

Geochemical insights into contribution of petroleum hydrocarbons to the formation of hydrates in the Taixinan Basin,the South China Sea

Methane hydrate in the South China Sea(SCS)has extensively been considered to be biogenic on the basis of itsδ13C and δD values.Although previous efforts have greatly been made,the contribution of thermogenic oil/gas has still been underestimated.In this study,biomarkers and porewater geochemical parameters in hydrate-free and hydrate-bearing sediments in the Taixinan Basin,the SCS have been measured for evaluating the contribu-tion of petroleum hydrocarbons to the formation of hydrate deposits via a comparative study of their source inputs of organic matters,environmental conditions,and microbial activities.The results reveal the occurrence of C14-C16 branched saturated fatty acids(bSFAs)with relatively high concentrations from sulfate-reducing bacteria(SRBs)in hydrate-bearing sediments in comparison with hydrate-free sediments,which is in accord with the positive δ13C values of dissolved inorganic carbon(DIC),increasing methane concentrations,decreasing alka-linity,and concentration fluctuation of ions(Cl-,Br,SO2-,Ca2+,and Mg2+).These data indicate the relatively active microbial activities in hydrate-bearing sediments and coincident variations of environmental conditions.Carbon isotope compositions of bSFAs(-34.0％o to-21.2％o),n-alkanes(-34.5％o to-29.3％o),and methane(-70.7％o to-69.9％o)jointly demonstrate that SRBs might thrive on a different type of organic carbon rather than methane.Combining with numerous gas/oil reservoirs and hydrocarbon migration channels in the SCS,the occurrence of unresolved complex mixtures(UCMs),odd-even predominance(OEP)values(about 1.0),and biomarker patterns suggest that petroleum hydrocarbons from deep oil/gas reservoirs are the most probable carbon source.Our new results provide significant evidence that the deep oil/gas reservoirs may make a contribution to the formation of methane hydrate deposits in the SCS.