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Petroleum potential of Baikal deposits 总被引：1，自引：0，他引：1
A.E. Kontorovich V.A. Kashirtsev V.I. Moskvin L.M. Burshtein T.I. Zemskaya E.A. Kostyreva G.V. Kalmychkov O.M. Khlystov 《Russian Geology and Geophysics》2007,48(12):1046-1053
We analyzed oils, gases, and bitumens of bottom sediments from natural shows on the southeastern shore of Lake Baikal, in the mouth of the Stvolovaya River near Capes Tolstyi and Gorevoi Utes. Based on a set of geological data, we have established that: (1) the lake oils underwent biodegradation to a variable degree: “Fresh” nondegraded paraffin oil floats up near Cape Gorevoi Utes; in the mouth of the Stvolovaya River and near Cape Tolstyi, aromatic-naphthene oil lacks n-alkanes, monomethyl alkanes, and acyclic isoprenoids; (2) Cenozoic oil originated from the organic matter of fresh-water basins with significant amounts of higher land plant remains, including angiosperm plants (oleanane), which suggests the lake or delta genesis of oil source formations of Cretaceous and younger ages. Judging from the carbon isotope composition (average δ13C = −43.84‰), methane from the bottom sediments near Cape Gorevoi Utes is catagenetic. The initial in-place resources in the Baikal sedimentary basins are estimated by the volumetric-statistical method at 500 mln tons of equivalent hydrocarbons. 相似文献
3.
I. A. Nemirovskaya 《Geochemistry International》2007,45(7):638-651
The abundances and compositions of aliphatic hydrocarbons (AHC) and polyaromatic hydrocarbons (PAH) were investigated in the water and bottom sediments of the southwestern Amur Bay in the Sea of Japan. The water contained from 0 to 129 μg/1AHC (averaging 42.2 μg/l) and from 5 to 85 ng/l PAH (averaging 18 ng/l). The bottom sediments contained 168–2098 μg/g AHC and 7.2–1100 ng/g dry mass PAH. It was shown that the input of anthropogenic HC is better recorded by molecular markers than the distribution of AHC and PAH concentrations. The discovery of elevated HC concentrations in the bottom water layer suggests that the bottom sediments induced secondary contamination of the water body. 相似文献
4.
Fredrick G. Prahl Joseph T Bennett Roy Carpenter 《Geochimica et cosmochimica acta》1980,44(12):1967-1976
Aliphatic hydrocarbon compositions were quantitatively characterized in plankton, sediment trap-collected particulate materials and sediments from Dabob Bay using high resolution glass capillary gas chromatography. The average net accumulation of individual hydrocarbons measured in a 1-yr series of sediment traps was compared with the net accumulation of corresponding compounds measured in three depth intervals of 210Pb-dated bottom sediments. Systematic and rapid decreases in the net accumulation of individual hydrocarbons were observed from the sediment traps to the sediments. Most pronounced decreases were measured for planktonically derived hydrocarbon constituents (e.g. pristane and two unsaturated compounds) which are rapidly remineralized at or near the sediment-water interface. Consequently, the amount of each compound measured in deposited sediments is not necessarily a quantitative indication of its initial flux to the sediments. The n-alkanes (C25,27,29,31). characteristic of terrestrial plant waxes, are the predominant hydrocarbons measured by 4–6 cm depth in these sediments and show reasonably constant net accumulation below this interval.Significant diagenetic alteration of the bulk organic matter contained in the average sediment trap particulate material is also noted through comparison with bottom sediments on the basis of organic C/N and δ13C measurements. Organic matter elementally similar to marine plankton is preferentially remineralized upon deposition of the sedimentary particulates. The residual organic matter remaining and buried in the bottom sediments closely resembles terrestrial organic matter. 相似文献
5.
Surface sediments from the Outer Continental Shelf of Alaska were analyzed for hydrocarbons as part of an environmental survey sponsored by NOAA/BLM. Sediments were collected from the proposed oil lease areas of Beaufort Sea, southeastern Bering Sea, Norton Sound, Navarin Basin, Gulf of Alaska, Kodiak Shelf and lower Cook Inlet. Data on normal and branched alkanes and di- and triterpenoids from capillary gas chromatography (GC) and gas chromatography-mass spectrometry (GC/ MS) indicate that the area displays little evidence of petroleum hydrocarbons (i.e., seeps) except at a few isolated stations. Beaufort Sea sediments have the highest hydrocarbon budget, whereas Kodiak Shelf sediments have the lowest. The molecular markers of the hydrocarbons are of a mixed marine autochthonous and terrestrial allochthonous origin. Norton Sound and Cook Inlet sediments contain the highest levels of terrigenous lipids and Kodiak Shelf the lowest. The abundance of alkenes implies that relatively low oxidizing conditions exist in some of the depositional areas studied, suggesting that extraneous petroleum hydrocarbons introduced into these sediments would be expected to have a relatively long residence time. The distribution of polynuclear aromatic hydrocarbons (PAH) is complex and shows a pyrolytic origin. The data on perylene strongly favor the hypothesis that it is “performed” from terrigenous precursors and transported into the marine environment with no apparent in situ generation. Polynuclear aromatic hydrocarbons of diagenetic origin are probably dominant in Gulf of Alaska and Kodiak Shelf sediments.Two stations, north of Kalgin Island, in lower Cook Inlet and one in southeastern Bering Sea show typical weathered petroleum distribution of n-alkanes and triterpenoids. Probable pathways of transport and fate of petroleum hydrocarbons in case of an oil spill are also briefly discussed. 相似文献
6.
The paper reviews data (acquired in 2007–2016) on aliphatic and polycyclic aromatic hydrocarbons in comparison with data on concentrations of lipids, Corg, and chlorophyll a in the water and bottom sediments the river–sea geochemical barrier (for the Northern Dvina, Ob, Yenisei, and Lena rivers). It was established that the concentrations of anthropogenic hydrocarbons decrease and these compounds precipitate like other organic compounds and particulate matter, where riverine and marine waters mix. Relatively pure water flows in the pelagic zones of seas. In spite of low temperatures in the Arctic, anthropogenic hydrocarbons transform so rapidly that natural compounds dominate in the water and bottom sediments: autochthonous in the seawater and allochthonous in the bottom sediments. 相似文献
7.
A. M. Nikonorov A. A. Matveev S. A. Reznikov V. S. Arakelyan N. N. Luk’yanova 《Doklady Earth Sciences》2012,443(1):361-364
New data on the concentration and spatial distribution of the benz(a)pyrene and polycyclic aromatic hydrocarbons in bottom
sediments in the testing area of the Baikal Pulp and Paper Plant (BPPP) waste water discharge in 1981–1988 and 2010 are presented
in this paper. The bottom sediments in this section of the lake are strongly polluted with polycyclic aromatic hydrocarbons. 相似文献
8.
A study of two classes of hydrocarbons (HCs)—aliphatic and polycyclic aromatic—in suspended matter of the surface waters and bottom sediments of the Northern and Middle Caspian Sea (R/V Nikifor Shurekov, October 2015) is described. It has been determined that oil pollution transported by river runoff and fluid streams flowing from sedimentary formations in the northeastern part are the main sources of hydrocarbons in the river–sea boundaries of the Volga, Terek, and Sulak rivers. 相似文献
9.
《Geochimica et cosmochimica acta》1987,51(6):1457-1466
Aliphatic and aromatic hydrocarbons in sediments of the middle and lower Mississippi Fan and two intraslope basins in the Gulf of Mexico are derived from terrestrial organic matter and thermogenic, mature hydrocarbons. The terrestrial hydrocarbon component consists primarily of terrigenous, plant biowaxes (n-alkanes with 21 to 33 carbons). The occurrence of thermogenic hydrocarbons in immature near-surface sediments, their molecular distributions and concentration variations with depth suggest that the majority of these mature hydrocarbons have migrated from a source much deeper in the sediment column. A portion of the thermogenic hydrocarbons may be derived from recycled material and includes phenanthrene, methyl phenanthrenes, chrysene and benzopyrenes. The migrated, thermogenic hydrocarbons include normal and isoprenoid alkanes with less than 21 carbons, naphthalene, methyl naphthalenes, ethyl naphthalenes and other aromatics of similar volatility (i.e., biphenyl, acenaphthene and fluorene). Triterpane, sterane and aromatized sterane distributions suggest that the thermogenic hydrocarbons at both sites have a common source and are overprinted with immature sediment hydrocarbons. The biomarker distributions and carbon isotopic compositions of the thermogenic hydrocarbons are atypical for petroleum produced in the Gulf of Mexico. Molecular distributions of the hydrocarbons are constant, regardless of the present depth of occurrence, suggesting that they have migrated in a separate phase. The upward migration of hydrocarbons from deeper sources is a wide-spread phenomenon in the Gulf of Mexico with several documented cases of massive seepage (visible oil) as well as the more diffuse permeation of Pleistocene sediments of the Mississippi Fan and two intraslopes reported here. 相似文献
10.
G. M. Friedman P. K. Mukhopadhyay A. Moch M. Ahmed 《International Journal of Coal Geology》2000,43(1-4)
The New York Bight is a sector of the Middle Atlantic continental shelf. The Bight consists of a part of the Atlantic Ocean offshore of the New York and New Jersey metropolitan area. This area includes the most populated coastal setting in North America. The Atlantic shelf and its estuaries are used for waste disposal, dredging, commercial fishing, and recreation; activities that contribute to the contamination of associated bottom sediments. Existing data for toxicants are still inadequate. Improvements in sediment and water quality will require a more detailed knowledge and understanding of sediments and water in the Bight. Eleven coring stations were established in New York Bight. Decreases in pH and Eh both above and below the water/sediment interface are attributed to the activity of anaerobic bacteria. Sulfate reduction is one of the important processes in lowering pH. Low Eh values of up to −443 can be related to sulfate-reducing bacteria. The highest negative Eh generally occurs with the highest organic carbon concentration. Core samples yielded up to 4.00% organic carbon compared to 0.8 to 1.2% in sediments of the natural nearshore environment. Twenty-seven different aliphatic hydrocarbons, fourteen PAHs, five cyclic hydrocarbons, and eight dicarboxylic acids were identified in the Bight pore waters. Sediment located deeper in the Hudson Shelf Valley has a greater abundance of aliphatic hydrocarbons as adsorbed pollution on clay and silt. The presence of dicarboxylic acids leached from plastic came from anthropogenic activities (mostly sewage). PAHs have two sources: coal ash (observed in sediments) and petroleum (part of the sewage, run-offs, and oil spills). The rest of the hydrocarbons have a petroleum or biogenic origin. The high amount of organic carbon may be the result of sewage sludge or originated from natural sources. The main sources of contaminants are dumpsites, emergency releases after heavy rainstorms from sewage-treatment plants, tanker washing, storage transfer spills, run-off, and air-borne pollution. The relatively high accumulation of organic matter causes oxygen depletion, which creates anaerobic conditions. The presence of hydrogen sulfide makes the environment toxic for most of the biota. Detected hydrocarbons, especially PAHs easily enter the food chain and may cause cancer and mutagenic reactions of biota and humans. Organic petrology of six organic-rich sediments from New York Harbor illustrates a diverse population of anthropogenic and natural organic components. Three core samples (V-2, AC-4, and HV-3) contain coarse-textured organic matter. A slim majority of those components are anthropogenic. They are derived mainly from coal combustion by-products. The other two core samples (AC-6 and T-1) contain mainly very fine-grained organic matter. A majority of them are amorphous organic matter (AOM) that is derived from bacterial degradation of modern organic matter. Radionuclide dating (137Cs, K-40, Pb-210) shows post-1950 components for the shallowest intervals in the cores (<30 cm). The post-1950 sediment, distributed in the tops of core, is recycled material from the dumpsites. The underlying sediment has isotopic signatures that suggest dates before active dumping. 相似文献
11.
近海油气藏渗漏烃的检测方法综述 总被引：7，自引：0，他引：7
主要总结了海域油气藏渗漏烃的航空遥感和地球化学检测方法.遥感测量可以从宏观上圈定海面油膜的分布范围,是海上油气藏勘探前期常用的廉价方法;海底沉积物取芯测量和海水嗅探器现场分析是海域油气藏渗漏烃地球化学检测的主要手段,海水样品的脱气处理是海水介质中渗漏烃地球化学检测的关键环节;海水和海底沉积物取样设备与脱气技术的不断完善,为海域油气藏渗漏烃的检测提供了基本保障;目前,底层水采样分析与海底沉积物取芯分析已成为一种有效且相对经济的海域油气藏渗漏烃检测技术组合,与一些地球物理方法结合应用,可有效地圈定海底下方渗漏源的位置. 相似文献
12.
无机生油假说认为,原油和天然气和近地表的生物物质没有根本联系,它们是生成于地幔内的非生物来源的碳氢化合物。因而油气不是一个不可再生资源,而是一个可再生资源。无机生油假说得到地质学、物理学和化学等三个基本学科的支持。在地质观察上,发现全球许多大油田的油气储藏与原始生物物质之间数量上有巨大落差,难于解释它们是由生物生成的。此外,有许多地区在结晶基底或变质基底内,或直接位于其上的沉积岩中发现石油。从生物生油假说来说,也是无法理解的。在化学上,早在二战期间,德国已由人工合成石油(费托合成),并生产了占德国战争中用油的9%的石油。无可争辩地说明,无机可以生成石油。根据化学(物理学)热力学理论分析确认,甲烷是唯一一种在标准温压条件(温度为298.15 K;压力为101325 Pa)下稳定的碳氢化合物,从甲烷形成正常烷属烃只有在压力>3×106kPa、温度>700°C时(相当于地下深度约100 km)才有可能。在地壳内的温压条件下由生物变质形成石油的假说,与化学热力学的基本原则相抵触。从氧化的有机分子,如碳水化合物(C6H12O6)形成较高的碳氢化合物在任何条件下都是不可能的。根据我国长期对深部构造的研究,笔者认为在中国东部及西太平洋蘑菇云岩石圈地幔发育的地区是寻找巨型无机油气田的有利地区,建议在发育蘑菇云岩石圈地幔地区开展无机油气田的勘探,并在无机油气田远景地区布置超深参数钻,以评价含油气远景。另外建议加强物探工作,尤其是研究地震勘探处理基底内三维含油气构造的技术。 相似文献
13.
Sources of fluids and gases expelled at cold seeps offshore Georgia, eastern Black Sea 总被引：1，自引：0，他引：1
Anja Reitz Thomas Pape Mark Schmidt Florian Scholz Giovanni Aloisi Stephan M. Weise 《Geochimica et cosmochimica acta》2011,75(11):3250-46
Four seep sites located within an ∼20 km2 area offshore Georgia (Batumi seep area, Pechori Mound, Iberia Mound, and Colkheti Seep) show characteristic differences with respect to element concentrations, and oxygen, hydrogen, strontium, and chlorine isotope signatures in pore waters, as well as impregnation of sediments with petroleum and hydrocarbon potential. All seep sites have active gas seepage, near surface authigenic carbonates and gas hydrates. Cokheti Seep, Iberia Mound, and Pechori Mound are characterized by oil-stained sediments and gas seepage decoupled from deep fluid advection and bottom water intrusion induced by gas bubble release. Pechori Mound is further characterized by deep fluid advection of lower salinity pore fluids. The Pechori Mound pore fluids are altered by mineral/water reactions at elevated temperatures (between 60 and 110 °C) indicated by heavier oxygen and lighter chlorine isotope values, distinct Li and B enrichment, and K depletion. Strontium isotope ratios indicate that fluids originate from late Oligocene strata. This finding is supported by the occurrence of hydrocarbon impregnations within the sediments. Furthermore, light hydrocarbons and high molecular weight impregnates indicate a predominant thermogenic origin for the gas and oil at Pechori Mound, Iberia Mound, and Colkheti Seep. C15+ hydrocarbons at the oil seeps are allochtonous, whereas those at the Batumi seep area are autochthonous. The presence of oleanane, an angiosperm biomarker, suggests that the hydrocarbon source rocks belong to the Maikopian Formation. In summary, all investigated seep sites show a high hydrocarbon potential and hydrocarbons of Iberia Mound, Colkheti Seep, and Pechori Mound are predominantly of thermogenic origin. However, only at the latter seep site advection of deep pore fluids is indicated. 相似文献
14.
Rohinton A. Noble Robert Alexander Robert Ian Kagi John Knox 《Geochimica et cosmochimica acta》1985,49(10):2141-2147
Tetracyclic diterpenoid hydrocarbons (diterpanes) based on the ent-beyerane, phyllocladane and ent-kaurane skeletons have been identified in the hydrocarbon extracts of some Australian coals, sediments and crude oils. Structures were assigned to the geological diterpanes by comparison with synthetically prepared reference compounds. Studies of a sample suite consisting of low-rank coals and sediments indicate that the ratios of C-16 epimers of phyllocladane and ent-kaurane are maturity dependent, and that the relative proportion of the thermodynamically preferred 16β (H)-compounds increases with increasing thermal maturity. Thermodynamic equilibrium for the interconversion reactions is attained in sediments before the onset of crude oil generation.The most likely natural product precursors for the tetracyclic diterpanes are considered to be the tetracyclic diterpene hydrocarbons which occur widely in the leaf resins of conifers. Tetracyclic diterpanes have been identified in sediments and coals of Permian age or younger, suggesting that these compounds are markers for both modern and extinct families of conifers. In particular, phyllocladane is proposed as a marker for the Podocarpaceae family of conifers. 相似文献
15.
The majority of the world's oil and gas deposits have been discovered by drilling in the vicinity of natural petroleum seeps, and to date the most successful geochemical prospecting methods still rely upon the surface detection of hydrocarbons. Gas chromatographic techniques are now commonly used in the analysis of hydrocarbon gases for prospecting both onshore (analysis of soils and rocks) and offshore (analysis of near-bottom waters and sediments). Detection of helium fluxes has been partially successful as a geochemical prospecting technique. Many indirect techniques such as the determination of isotope and metal-leaching anomalies in surface rocks and the measurement of radon fluxes have not been widely used.Onshore geochemical prospecting appears to have more problems associated with it than offshore prospecting due to the more complex migration mechanism of near-surface waters containing dissolved gases. No onshore prospecting studies have been published which thoroughly consider this factor and the success of onshore prospecting remains equivocal. In offshore prospecting “sniffers” have been used to detect hydrocarbon anomalies in near-bottom waters, and coring equipment has been used for the detection of hydrocarbons in near-surface sediments. Success is claimed using these techniques.Geochemical prospecting methods are complementary to the widely used geophysical methods. Geochemical methods can provide direct evidence for the presence of petroleum accumulations and are relatively cheap and rapid. Failures in prospecting to date are attributable to the simplistic manner in which data have been interpreted; insufficient attention has been paid to the hydrological and geological factors which modify the upward migration of indicator species to the surface. As oil and gas deposits become more difficult to locate, greater attention should be paid to geochemical prospecting techniques, especially as a regional exploration tool. 相似文献
16.
T.G. Powell 《Journal of Geochemical Exploration》1975,4(4):441-466
An organic geochemical study has been made of sediments from five petroleum exploration wells and liquid hydrocarbons from seven oil and gas condensate discoveries in the offshore Dampier Sub-basin. Hydrocarbon generation has occurred between 3000 and 4250 m and the probable source rocks have been identified. Oils and condensates in the basin are of two types; a paraffinic-naphthenic type derived from Jurassic source beds and a naphthenic type coming from Cretaceous source sediments. Mixing of the two oil types appears to have occurred in the Egret reservoir. 相似文献
17.
Characterization and source apportionment of polycyclic aromatic hydrocarbons (PAHs) in sediments in the Yellow River Estuary, China 总被引：3，自引：0，他引：3
Ning-jing Hu Peng Huang Ji-hua Liu De-yi Ma Xue-fa Shi Jian Mao Ying Liu 《Environmental Earth Sciences》2014,71(2):873-883
Concentrations and sources of polycyclic aromatic hydrocarbons (PAHs) were investigated in surface sediments of the Yellow River Estuary (YRE). The isobath-parallel tidal and residual currents play important roles in the variation of PAH distribution, such that the contamination level of PAHs in fine-grained sediments is significantly higher than in the relatively coarse grain size sediments. Both diagnostic ratios and principal component analysis (PCA) with multivariate linear regression (MLR) were used to apportion sources of PAHs. The results revealed that pyrogenic sources are important sources of PAHs. Further analysis indicated that the contributions of coal combustion, traffic-related pollution and mixed sources (spills of oil products and vegetation combustion) were 35, 29 and 36 %, respectively, using PCA/MLR. Pyrogenic sources (coal combustion and traffic-related pollution) contribute 64 % of anthropogenic PAHs in sediments, which indicates that energy consumption could be a predominant factor in PAH pollution of YRE. Acenaphthylene and acenaphthene are the two main species of PAHs with more ecotoxicological concern in YRE. 相似文献
18.
氨基酸、脂肪酸对过渡带气、低熟原油形成的意义 总被引：21，自引：4，他引：21
对草海盆地泥炭、柴窝堡盆地第四系沉积物以及辽河东部凹陷、胜利东营凹陷、苏北金湖凹陷等第三系烃源岩中氨基酸、脂肪酸进行定性、定量分析，并开展热模拟实验。研究表明氨基酸主要赋存于沥青中，分解后可以生成烃类气体和Ｎ２气，对过渡带气的形成可作出贡献。烃源岩干酪根和沥青中的脂肪酸含量不少，沥青中脂肪酸以一元酸为主，具偶碳优势，干酪根中脂肪酸以二元酸为主，不具偶碳优势。沥青和干酪根中脂肪酸脱羧基后产生烷烃，对过渡带气和低熟油都可作出贡献，沥青中脂肪酸是生成低熟油中具奇碳优势正烷烃的主要物源。 相似文献
19.
对松花江底积物中16种多环芳烃类化合物(PAHs)进行调查结果显示,松花江底积物中属于美国EPA优先控制的16种PAHs全被检出。16种PAHs总含量范围226.86～10079.68 ng.g-1,平均含量为2230.04 ng.g-1。其中,4环和5～6环PAHs的相对丰度为61.6%,2～3环PAHs的相对丰度为38.4%,研究表明松花江底积物中PAHs主要来源于生物化石燃料燃烧,仅支流嫩江齐齐哈尔下游段、干流肇源县西段主要体现为石油类输入。就松花江PAHs生态风险而言:在第二松花江吉林市上游、吉林市下游段,PAHs遍及低环、中环、高环都超过了生态效应警戒值低值(ERL);嫩江支流泰来东南段PAHs组分萘(Nap)、苊(Ace)、芴(Fl),松花江干流巴彦段二苯并[a,h]蒽(DBA)也超过了生态效应警戒值低值(ERL)。这说明这些超ERL值的河段底积物中PAHs对裸露生物体的毒副作用风险率大于10%,具有一定的潜在生态风险。 相似文献
20.
Yan Li Yun-Xin Fang Qian-Zhi Zhou Xiang-Po Xu Jin-Zhong Liu Guo-Yi Zhou Jiang-Hai Wang 《地学前缘(英文版)》2021,12(6):394-403
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. 相似文献