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1.
Gas occurrences consisting of carbon dioxide (CO2), hydrogen sulfide (H2S), and hydrocarbon (HC) gases and oil within the Dodan Field in southeastern Turkey are located in Cretaceous carbonate reservoir rocks in the Garzan and Mardin Formations. The aim of this study was to determine gas composition and to define the origin of gases in Dodan Field. For this purpose, gas samples were analyzed for their molecular and isotopic composition. The isotopic composition of CO2, with values of −1.5‰ and −2.8‰, suggested abiogenic origin from limestone. δ34S values of H2S ranged from +11.9 to +13.4‰. H2S is most likely formed from thermochemical sulfate reduction (TSR) and bacterial sulfate reduction (BSR) within the Bakuk Formation. The Bakuk Formation is composed of a dolomite dominated carbonate succession also containing anhydrite. TSR may occur within an evaporitic environment at temperatures of approximately 120–145 °C. Basin modeling revealed that these temperatures were reached within the Bakuk Formation at 10 Ma. Furthermore, sulfate reducing bacteria were found in oil–water phase samples from Dodan Field. As a result, the H2S in Dodan Field can be considered to have formed by BSR and TSR.As indicated by their isotopic composition, HC gases are of thermogenic origin and were generated within the Upper Permian Kas and Gomaniibrik Formations. As indicated by the heavier isotopic composition of methane and ethane, HC gases were later altered by TSR. Based on our results, the Dodan gas field may have formed as a result of the interaction of the following processes during the last 7–8 Ma: 1) thermogenic gas generation in Permian source rocks, 2) the formation of thrust faults, 3) the lateral-up dip migration of HC-gases due to thrust faults from the Kas Formation into the Bakuk Formation, 4) the formation of H2S and CO2 by TSR within the Bakuk Formation, 5) the vertical migration of gases into reservoirs through the thrust fault, and 6) lateral-up dip migration within reservoir rocks toward the Dodan structure.  相似文献   

2.
Intense thermochemical sulfate reduction (TSR) and up to 18% H2S are found in the Upper Permian Changxing Formation (P3ch) in the northeast (NE) Sichuan Basin, China, despite that rare gypsum or anhydrite was found in this formation. Here, we present new concentration data of carbonate-associated sulfate (CAS) from carbonate host rocks, C, O, and Sr isotope data for TSR-related calcites, and S isotope data for sulfur compounds obtained during this study. These data along with spatial-temporal changes in palaeogeopressure conditions, hydraulic conductivity and the physical capacity indicate that the H2S was generated locally from TSR within the P3ch reservoirs. We propose that the reactive sulfates were derived from CAS released during dolomitization and recrystallization of earlier dolomite within the P3ch Fm. and from the cross-formational migration of evaporative brines from the Lower Triassic Feixianguan Formation (T1f) to P3ch Fm. Our calculation shows that the two sources could provide enough SO42− for the generation of H2S within the P3ch reservoirs. Early downward migration of sulfate-rich evaporative brines from the T1f formation occurred in near-surface and shallow burial diagenetic settings (mainly <1000 m). The evaporative brines seeped into porous grainstones and displaced preexisting seawater, causing pervasive dolomitization within the P3ch Fm. Subsequently, TSR calcites precipitated from the pore water have high Sr concentrations (up to 7767 ppm), close to the T1f TSR calcites, and 87Sr/86Sr ratios mainly from 0.7074 to 0.7078, which are significantly higher than those of Late Permian seawater but within the range of early Triassic seawater.  相似文献   

3.
New sour pools have recently found in the Lower Triassic Feixianguan Fm carbonate reservoirs in the East Sichuan Basin in China with H2S up to 17.4% by volume. A recent blowout from a well drilled into this formation killed hundreds of people as a result of the percentage concentrations of H2S. In order to assess the origin of fatal H2S as well as the cause of petroleum alteration, H2S concentrations and the isotopes, δ34S and δ13C have been collected and measured in gas samples from reservoirs. Anhydrite, pyrite and elemental sulphur δ34S values have been measured for comparison. The high concentrations of H2S gas are found to occur at depths >3000 m (temperature now at 100 °C) in evaporated platform facies oolitic dolomite or limestone that contains anhydrite nodule occurrence within the reservoirs. Where H2S concentrations are greater than 10% its δ34S values lie between +12.0 and +13.2‰ CDT. This is within the range of anhydrite δ34S values found within the Feixianguan Fm (+11.0 to +21.7‰; average 15.5±3.5‰ CDT). Thus H2S must have been generated by thermochemical sulphate reduction (TSR) locally within the reservoirs. Burial history analysis and fluid inclusion data reveal that the temperature at which TSR occurred was greater than about 130–140 °C, suggesting that the present depth-temperature minimum is an artifact of post-TSR uplift. Both methane and ethane were actively involved in TSR since the petroleum became almost totally dry (no alkanes except methane) and methane δ13C values become significantly heavier as TSR proceeded. Methane δ13C difference thus reflects the extent of TSR. While it is tempting to use a present-day depth control (>3000 m) to predict the distribution of H2S in the Feixianguan Fm, this is an invalid approach since TSR occurred when the formation was buried some 1000–2000 m deeper than it is at present. The likelihood of differential uplift across the basin means that it is important to develop a basinal understanding of the thermal history of the Feixianguan Fm so that it is possible to determine which parts of the basin have been hotter than 130–140 °C.  相似文献   

4.
The Qiongdongnan Basin, South China Sea has received huge thickness (>12 km) of Tertiary-Quaternary sediments in the deepwater area to which great attention has been paid due to the recent discoveries of the SS22-1 and the SS17-2 commercial gas fields in the Pliocene-Upper Miocene submarine canyon system with water depth over 1300 m. In this study, the geochemistry, origin and accumulation models of these gases were investigated. The results reveal that the gases are predominated by hydrocarbon gases (98%–99% by volume), with the ratio of C1/C1-5 ranging from 0.92 to 0.94, and they are characterized by relatively heavy δ13C1 (−36.8‰ to −39.4‰) and δDCH4 values (−144‰ to −147‰), similar to the thermogenic gases discovered in the shallow water area of the basin. The C5-7 light hydrocarbons associated with these gases are dominated by isoparaffins (35%–65%), implying an origin from higher plants. For the associated condensates, carbon isotopic compositions and high abundance of oleanane and presence of bicadinanes show close affinity with those from the YC13-1 gas field in the shallow water area. All these geochemical characteristics correlate well with those found in the shales of the Oligocene Yacheng Formation in the Qiongdongnan Basin. The Yacheng Formation in the deepwater area has TOC values in the range of 0.4–21% and contains type IIb–III gas-prone kerogens, indicating an excellent gas source rock. The kinetic modeling results show that the δ13C1 values of the gas generated from the Yacheng source rock since 3 or 4 Ma are well matched with those of the reservoir gases, indicating that the gas pool is young and likely formed after 4 Ma. The geologic and geochemical data show that the mud diapirs and faults provide the main pathways for the upward migration of gases from the deep gas kitchen into the shallow, normally pressured reservoirs, and that the deep overpressure is the key driving force for the vertical and lateral migration of gas. This gas migration pattern implies that the South Low Uplift and the No.2 Fault zone near the deepwater area are also favorable for gas accumulation because they are located in the pathway of gas migration, and therefore more attention should be paid to them in the future.  相似文献   

5.
Natural gas samples from two gas fields located in Eastern Kopeh-Dagh area were analyzed for molecular and stable isotope compositions. The gaseous hydrocarbons in both Lower Cretaceous clastic reservoir and Upper Jurassic carbonate reservoir are coal-type gases mainly derived from type III kerogen, however enriched δD values of methane implies presence of type II kerogen related material in the source rock. In comparison Upper Jurassic carbonate reservoir gases show higher dryness coefficient resulted through TSR, while presence of C1C5 gases in Lower Cretaceous clastic reservoir exhibit no TSR phenomenon. Carbon isotopic values indicate gas to gas cracking and TSR occurrence in the Upper Jurassic carbonate reservoir, as the result of elevated temperature experienced, prior to the following uplifts in last 33–37 million years. The δ13C of carbon dioxide and δ34S of hydrogen sulfide in Upper Jurassic carbonate reservoir do not primarily reflect TSR, as uplift related carbonate rock dissolution by acidic gases and reaction/precipitation of light H2S have changed these values severely. Gaseous hydrocarbons in both reservoirs exhibit enrichment in C2 gas member, with the carbonate reservoir having higher values resulted through mixing with highly-mature-completely-reversed shale gases. It is likely that the uplifts have lifted off the pressure on shale gases, therefore facilitated the migration of the gases into overlying horizons. However it appears that the released gases during the first major uplift (33–37 million years ago) have migrated to both reservoirs, while the second migrated gases have only mixed with Upper Jurassic carbonate reservoir gases. The studied data suggesting that economic accumulations of natural gas/shale gases deeper than Upper Jurassic carbonate reservoir would be unlikely.  相似文献   

6.
The processes involved in the interaction between organic fluids and carbonates, and the resulting effect on reservoir quality during the evolution and maturation of organic matter remain unclear despite the fact that these processes influence the carbon and oxygen isotopic compositions of carbonates. Here, we provide new insights into these processes using data obtained from a detailed analysis of a mixed dolomitic–clastic and organic-rich sedimentary sequence within the middle Permian Lucaogou Formation in the Junggar Basin of NW China. The techniques used during this study include drillcore observations, thin section petrography, scanning electron microscopy (SEM) and electron probe microanalysis, and carbon and oxygen isotope analyses. Oil grades and total organic carbon (TOC) contents represent the amount of oil charging and the abundance of organic fluids within a reservoir, respectively, and both negatively correlate with the whole-rock δ13C and δ18O of the carbonates in the study area, indicating that organic fluids have affected the reservoir rocks. Secondary carbonates, including sparry calcite and dolomite overgrowths and cements, are common within the Lucaogou Formation. Well-developed sparry calcite is present within dark mudstone whereas the other two forms of secondary carbonates are present within the dolomite-rich reservoir rocks in this formation. Comparing thin section petrology with δ13C compositions suggests that the carbon isotopic composition of matrix carbonates varies little over small distances within a given horizon but varies significantly with stratigraphic height as a result of the development of secondary carbonates. The net change in whole-rock δ13C as a result of these secondary carbonates ranges from 1.8‰ to 4.6‰, with the secondary carbonates having calculated δ13C compositions from −18.6‰ to −8.5‰ that are indicative of an organic origin. The positive correlation between the concentration of Fe within matrix and secondary carbonates within one of the samples suggests that the diagenetic system within the Lucaogou Formation was relatively closed. The correlation between δ13C and δ18O in carbonates is commonly thought to be strengthened by the influence of meteoric water as well as organic fluids. However, good initial correlation between δ13C and δ18O of whole rock carbonates within the Lucaogou Formation (resulted from the evaporitic sedimentary environment) was reduced by organic fluids to some extent. Consequently, the δ13C–δ18O covariations within these sediments are not always reliable indicators of diagenetic alteration by organic fluids or meteoric water.The characteristics and δ13C compositions of the sparry calcite within the formation is indicative of a genetic relationship with organic acids as a result of the addition of organic CO2 to the reservoir. Further analysis suggests that both carbonate and feldspar were dissolved by interaction with organic CO2. However, dissolved carbonate reprecipitated as secondary carbonates, meaning that the interaction between organic fluids and dolomites did not directly improve reservoir quality, although this process did enhance the dissolution of feldspar and increase porosity. This indicates that the δ13C and δ18O of secondary carbonates and their influence on whole-rock carbonate isotopic values can be used to geochemically identify the effect of organic fluids on closed carbonate-rich reservoir systems.  相似文献   

7.
Ancient hydrocarbon seepage occurred in the Hrabůvka quarry at the boundary between the basement of the Bohemian Massif (represented by folded Lower Carboniferous siliciclastics of the Culm facies) and Tertiary sedimentary cover of the Carpathian Foredeep (formed by Lower Badenian siliciclastics and calcareous clays). The unconsolidated Lower Badenian sediments contain lithified domains composed of limestone and breccias with limestone cement, whereas the basement rocks are cut by subvertical neptunic dykes filled up by limestone and calcite-marcasite-pyrite veinlets representing sealed fluid conduits. The deeply negative δ13C values of both vein calcite and limestone (down to −38.1‰ V-PDB) indicate that oxidation of hydrocarbons was the major source of carbon for authigenic mineralization. A fluid inclusion study suggests low fluid temperatures (<50 °C) and low and variable salinities of aqueous fluids associated with hydrocarbons (0.7–6.7 wt. % NaCl eq.). The variability of δ18O values of authigenic carbonates (−1.7 to −8.2‰ V-PDB) could reflect either slight changes in temperature of escaping fluids (mostly within 15 °C), and/or some mixing with meteoric waters. The low δ34S values of vein marcasite (∼–20‰ V-CDT) are consistent with bacterial reduction of sulfate in the hydrothermal system. Low C1/(C2+C3) ratios in hydrocarbon gas extracted from authigenic carbonates (9.9 and 5.8) as well as the high δ13C values of methane (−31.8 and −32.4‰ V-PDB) are compatible with a thermogenic source of hydrocarbons. REE data indicate sequestration of REE from finely dispersed detrital material in the apical part of the hydrothermal system. The available data are compatible with two possible scenarios of fluid origin. The hydrocarbons could have been leached from underlying Paleozoic sedimentary sequence by aqueous fluids that infiltrated into the basement after Tertiary tectonic reactivation. Alternatively, an external source of hydrocarbon-bearing fluids can be found in the adjacent Outer Western Carpathians flysch nappes containing petroleum-producing lithologies. Nevertheless, a regional flow of hydrocarbon-bearing fluids is evidenced by the occurrence of very similar hydrocarbon-bearing vein mineralizations in a wider area.  相似文献   

8.
Poor biostratigraphic control for some Triassic-Jurassic successions in the North Sea Basin and sub-basins necessitates the use of alternative correlation methods. This study examines the use of diagenetic signatures to distinguish continenetal from marine sandstone successions (Triassic-Jurassic) in the UK Central Graben. The key diagenetic alterations encountered in these successions include kaolinitization of the framework grains and the development of sphaerosiderite and pyrite. The δ 13CV-PDB values of siderite (−8.1 to −8.5‰) and of ankerite (−10.8 to −9.2‰), indicate a strong contribution of dissolved carbon from the decay of plant material in soil. However, marine water likely influenced diagenesis during periods of relative sea level rise by providing the dissolved sulfate (SO42−) required for the precipitation of pyrite. The presence of diagenetic alterations such as kaolinitization of framework grains and cementation by sphaerosiderite could indicate that the sediments were deposited in an overall continental setting. However, the occurrence of pyrite and scattered grains of deep-green colored glauconite suggests occasional marine influence. Such information on the changes of the diagenetic realm provides important clues for establishing a framework for stratigraphic correlations. Caution should be exercised when interpreting petrographic data as subsequent episodes of telodiagenesis can complicate petrographic interpretations.  相似文献   

9.
Deeply buried (4500–7000 m) Ordovician carbonate reservoirs in the Tazhong area, Tarim Basin, NW China show obvious heterogeneity with porosity from null in limestones and sweet dolostones to 27.8% in sour dolostones, from which economically important oils, sour gas and condensates are currently being produced. Petrographic features, C, O, Sr isotopes were determined, and fluid inclusions were analyzed on diagenetic calcite, dolomite and barite from Ordovician reservoirs to understand controls on the porosity distribution. Ordovician carbonate reservoirs in the Tazhong area are controlled mainly by initial sedimentary environments and eo-genetic and near-surface diagenetic processes. However, vugs and pores generated from eogenetic and telogenetic meteoric dissolution were observed to have partially been destroyed due to subsequent compaction, filling and cementation. In some locations or wells (especially ZG5-ZG7 Oilfield nearby ZG5 Fault), burial diagenesis (e.g. thermochemical sulfate reduction, TSR) probably played an important role in quality improvement towards high-quality reservoirs. C2 calcite and dolomite cements and barite have fluid inclusions homogenization temperatures (Ths) from 86 to 113 °C, from 96 to 128 °C and from 128 to 151 °C, respectively. We observed petrographically corroded edges of these high-temperature minerals with oil inclusions, indicating the dissolution must have occurred under deep-burial conditions. The occurrence of TSR within Ordovician carbonate reservoirs is supported by C3 calcite replacement of barite, and the association of sulfur species including pyrite, anhydrite or barite and elemental sulfur with hydrocarbon and 12C-rich (as low as −7.2‰ V-PDB) C3 calcite with elevated Ths (135–153 °C). The TSR may have induced burial dissolution of dolomite and thus probably improved porosity of the sour dolostones reservoirs at least in some locations. In contrast, no significant burial dissolution occurred in limestone reservoirs and non-TSR dolostone reservoirs. The deeply buried sour dolostone reservoirs may therefore be potential exploration targets in Tarim Basin or elsewhere in the world.  相似文献   

10.
This study investigates the source rock characteristics of Permian shales from the Jharia sub-basin of Damodar Valley in Eastern India. Borehole shales from the Raniganj, Barren Measure and Barakar Formations were subjected to bulk and quantitative pyrolysis, carbon isotope measurements, mineral identification and organic petrography. The results obtained were used to predict the abundance, source and maturity of kerogen, along with kinetic parameters for its thermal breakdown into simpler hydrocarbons.The shales are characterized by a high TOC (>3.4%), mature to post-mature, heterogeneous Type II–III kerogen. Raniganj and Barren Measure shales are in mature, late oil generation stage (Rr%Raniganj = 0.99–1.22; Rr%Barren Measure = 1.1–1.41). Vitrinite is the dominant maceral in these shales. Barakar shows a post-mature kerogen in gas generation stage (Rr%Barakar = 1.11–2.0) and consist mainly of inertinite and vitrinite. The δ13Corg value of kerogen concentrate from Barren Measure shale indicates a lacustrine/marine origin (−24.6–−30.84‰ vs. VPDB) and that of Raniganj and Barakar (−22.72–−25.03‰ vs. VPDB) show the organic provenance to be continental. The δ13C ratio of thermo-labile hydrocarbons (C1–C3) in Barren Measure suggests a thermogenic source.Discrete bulk kinetic parameters indicate that Raniganj has lower activation energies (ΔE = 42–62 kcal/mol) compared to Barren Measure and Barakar (ΔE = 44–68 kcal/mol). Temperature for onset (10%), middle (50%) and end (90%) of kerogen transformation is least for Raniganj, followed by Barren Measure and Barakar. Mineral content is dominated by quartz (42–63%), siderite (9–15%) and clay (14–29%). Permian shales, in particular the Barren Measure, as inferred from the results of our study, demonstrate excellent properties of a potential shale gas system.  相似文献   

11.
Methane is a useful tracer for studying hydrothermal discharge, especially where the source fluids are of low temperature and lack metal precipitates. However, the dual origins of deep-sea methane, both chemical and biological, complicate the interpretation of methane observations. Here, we use both the concentration and stable carbon isotopic composition (δ13C) of dissolved methane to trace hydrothermal plumes and identify the source and behavior of methane at two sites of newly discovered hydrothermal activity on the Central Indian Ridge (11–13°S). At both sites, methane and optical anomalies between 2500 and 3500 m at all stations indicate active hydrothermal discharge. We compared methane concentrations and δ13C at three stations, two (CTIR110136 and CTIR110208) with the most prominent anomalies at each site, and a third (CTIR110140) with near-background methane values. At stations CTIR110136 and CTIR110208, the concentration and δ13C of methane in distinct plumes ranged from 3.3 to 42.3 nmol kg−1 and −30.0 to −15.4‰, respectively, compared to deep-water values of 0.5 to 1.2 nmol kg−1 and −35.1 to −28.9‰ at the station with a near-background distal plume (CTIR110140). δ13C was highest in the center of the plumes at CTIR110136 (−15.4‰) and CTIR110208 (−17.8‰). From the plume values we estimate that the δ13C of methane in the hydrothermal fluids at these stations was approximately −19‰ and thus the methane was most likely derived from magmatic outgassing or the chemical synthesis of inorganic matter. We used the relationship between δ13C and methane concentration to examine the behavior of methane at the plume stations. In the CTIR110208 plume, simple physical mixing was likely the major process controlling the methane profile. In the CTIR110136 plume we interpret a more complicated relationship as resulting from microbial oxidation as well as physical mixing. We argue that this difference in methane behavior between the two areas stems from a distinct bathymetric dissimilarity between the two stations. The location of CTIR110208 on the open slope of a ridge allowed rapid plume dispersion and physical mixing, whereas the location of CTIR110136 in a small basin surrounded by wall structures inhibited physical mixing and enhanced microbial oxidation.  相似文献   

12.
Authigenic carbonates are frequently associated with methane cold-seep systems, which extensively occur in various geologic settings worldwide. Of interest is the relation between the fluids involved in their formation and the isotopic signals recorded in the carbonate cements. Along the Northern Apennines foothills (Italy), hydrocarbons and connate waters still seeping nowadays are believed to be the primary sources for the formation of fossil authigenic carbonate found in Plio-Pleistocene marine sediments. Four selected outcrops of dolomitic authigenic carbonates were analysed to compare signature of seeping fluids with fractionation of stable carbon and oxygen isotopes recorded in the carbonate.Along the foothills, deep methane-rich fluids spontaneously rise to the surface through mud volcanoes or are exploited in wells drilled nearby to the fossil Plio-Pleistocene authigenic carbonates. The plumbing system providing fluids to present-day cold seeps was structurally achieved in Late Miocene and Plio-Pleistocene. δ13C values of methane, which vary from −51.9 to −43.0‰ VPDB, indicate that gas composition from the deep hydrocarbon reservoirs is relatively uniform along the foothills. On the contrary, δ13C in fossil authigenic carbonates strongly varies among different areas and also within the same outcrop.The different carbon sources that fed the investigated carbonates were identified and include: thermogenic methane from the deep Miocene reservoirs, 13C-enriched CO2 derived from secondary methanogenesis and microbial methane from Pliocene successions buried in the Po Plain. The δ13C variability documented among samples from a single outcrop testifies that the authigenic carbonates might represent a record of varying biogeochemical processes in the hydrocarbon reservoirs. The sources of stable oxygen isotopes in authigenic carbonates are often ascribed to marine water. Oxygen isotopic fractionation in the dolomite cements indicates that marine pore water couldn't be the sole source of oxygen. δ18O values provide a preliminary evidence that connate waters had a role in the carbonates precipitation. The concomitant occurrence of active cold seepages and fossil record of former plumbing systems suggests that generation and migration of hydrocarbons are long-lasting and very effective processes along the Northern Apennines foothills.  相似文献   

13.
A very high-resolution carbon and oxygen stable isotope analysis (bulk-carbonate) of a biostratigraphically well-constrained Callovian–Oxfordian series is provided here for the first time. The homogeneity of the clayey series and the weak diagenetic alteration allow the isotopic signal variations to be considered as primary in origin. A prominent and brief negative excursion in the δ13C curve (−2‰), occurring at the start of the Middle Callovian (Jason Zone – Obductum Subzone) and correlated regionally, suggests a possible methane release. The increasing δ13C values thereafter up to the Early Oxfordian, concomitant with a warming episode, highlight the burial of carbon in organic-rich layers which, in return, may have triggered a decrease in atmospheric pCO2. At higher frequencies, observed fluctuations of the δ13C and δ18O values are orbitally driven (405-kyr and 100-kyr eccentricity cycles) and may correspond to the salinity and temperature variability recorded in sea water. The δ18O isotopic measurements from well-preserved diagenetically screened belemnites and bivalves along the series, compared to available data from Tethyan domains, agree with the scenario of a global cooling at the Middle-Late Jurassic transition. The well-dated δ18O isotopic curve suggests that the onset of this cooling event occurred at the end of the Coronatum Zone (Middle Callovian).  相似文献   

14.
The stable carbon isotopic ratios (δ13C) of methane (CH4) and carbon dioxide (CO2) of gas-rich fluid inclusions hosted in fracture-fill mineralization from the southern part of the Lower Saxony Basin, Germany have been measured online using a crushing device interfaced to an isotopic ratio mass spectrometer (IRMS). The data reveal that CH4 trapped in inclusions seems to be derived from different source rocks with different organic matter types. The δ13C values of CH4 in inclusions in quartz hosted by Carboniferous rocks range between −25 and −19‰, suggesting high-maturity coals as the source of methane. Methane in fluid inclusions in minerals hosted by Mesozoic strata has more negative carbon isotope ratios (−45 to −31‰) and appears to represent primary cracking products from type II kerogens, i.e., marine shales. There is a positive correlation between increasing homogenization temperatures of aqueous fluid inclusions and less negative δ13C(CH4) values of in co-genetic gas inclusions probably indicating different mtaturity of the potential source rocks at the time the fluids were released. The CO2 isotopic composition of CH4-CO2-bearing inclusions shows slight negative or even positive δ13C values indicating an inorganic source (e.g., water-rock interaction and dissolution of detrital, marine calcite) for CO2 in inclusions. We conclude that the δ13C isotopic ratios of CH4-CO2-bearing fluid inclusions can be used to trace migration pathways, sources of gases, and alteration processes. Furthermore, the δ13C values of methane can be used to estimate the maturity of the rocks from which it was sourced. Results presented here are further supported by organic geochemical analysis of surface bitumens which coexist with the gas inclusion-rich fracture-fill mineralization and confirm the isotopic interpretations with respect to fluid source, type and maturity.  相似文献   

15.
To study the sedimentary environment of the Lower Cambrian organic-rich shales and isotopic geochemical characteristics of the residual shale gas, 20 black shale samples from the Niutitang Formation were collected from the Youyang section, located in southeastern Chongqing, China. A combination of geochemical, mineralogical, and trace element studies has been performed on the shale samples from the Lower Cambrian Niutitang Formation, and the results were used to determine the paleoceanic sedimentary environment of this organic-rich shale. The relationships between total organic carbon (TOC) and total sulfur (TS) content, carbon isotope value (δ13Corg), trace element enrichment, and mineral composition suggest that the high-TOC Niutitang shale was deposited in an anoxic environment and that the organic matter was well preserved after burial. Stable carbon isotopes and biomarkers both indicate that the organic matter in the Niutitang black shales was mainly derived from both lower aquatic organisms and algaes and belong to type I kerogen. The oil-prone Niutitang black shales have limited residual hydrocarbons, with low values of S2, IH, and bitumen A. The carbon isotopic distribution of the residual gas indicate that the shale gas stored in the Niutitang black shale was mostly generated from the cracking of residual bitumen and wet gas during a stage of significantly high maturity. One of the more significant observations in this work involves the carbon isotope compositions of the residual gas (C1, C2, and C3) released by rock crushing. A conventional δ13C1–δ13C2 trend was observed, and most δ13C2 values of the residual gases are heavier than those of the organic matter (OM) in the corresponding samples, indicating the splitting of ethane bonds and the release of smaller molecules, leading to 13C enrichment in the residual ethane.  相似文献   

16.
《Marine Geology》2001,172(3-4):197-204
The original stable isotopic composition of low-Mg calcitic planktic foraminifer tests is preserved in Pleistocene shallow-marine carbonates (in the Ryukyu Group; Okinawa, Japan) that have been altered by meteoric diagenesis. Whole-rock analyses indicate depleted isotopic values for both δ13C (−1.9 to −5.4‰) and δ18O (−2.9 to −5.2‰), as well as carbonate mineralogy exclusively composed of low-Mg calcite. However, analysis of carefully-extracted planktic foraminifer tests (Globigerinoides sacculifer) that were separated from these whole-rock samples yield heavier δ13C values (−0.4 to 1.9‰) and δ18O values (−3.2 to −1.0‰). The foraminiferal values themselves and comparison of values of various components suggest that the low-Mg calcite tests preserve the original stable isotopic values. Subsequently, the downcore δ18O change of planktic foraminifers recorded in the Ryukyu Group results from middle Pleistocene glacial–interglacial change. By comparison, isotopic measurements based on whole-rock samples can be obtained diagenetic environmental signals, but misleading with regard to paleoclimatic inferences.  相似文献   

17.
This paper presents an integrated assessment of total organic carbon, Rock-Eval pyrolysis, carbonate δ13C and δ18O, and total organic carbon δ13C record of Upper Sinemurian–Aalenian age from the Slyne Basin (well 18/25-1), offshore Ireland. Total organic carbon (up to 5.2 wt%) and Rock-Eval pyrolysis data highlights the Portree Shale Formation Equivalent (Lower–?Middle Toarcian) as a mature (Tmax ∼440 °C) source rock dominated by type II kerogens. This interval is more than 90 m thick.In a previously unexplored paleogeographical domain regarding stable carbon isotopes, the δ13C record shows positive values during the Upper Sinemurian, a negative trend followed by a minor positive trend during the uppermost Sinemurian–Lower Pliensbachian, a negative trend during the lowermost Lower Toarcian, and then the return to more positive δ13C values. Despite the biostratigraphic uncertainty, the coarse resolution of the dataset, and the complex assessment of diagenetic effects, we suggest that the δ13C record of the studied well records the Raricostatum Zone positive CIE, the Sinemurian-Pliensbachian Boundary Event, and the negative CIE associated with the T-OAE. The T-OAE positive CIE is not clearly defined in the obtained dataset. The slight post T-OAE negative CIE recovery to more positive values and the continuation of a relatively high organic content is coeval with a regional organic matter preservation interval observed in several Northern-European locations.These new datasets and their interpretation add to the understanding of the paleoenvironmental dynamics during the Early–?Middle Jurassic in the Northern European domain and opens new possibilities for hydrocarbon exploration in Ireland's offshore.  相似文献   

18.
Extensive, large-scale pervasive cementation in the form of cement bodies within fluvial strata has rarely been documented although fluvial strata commonly act as important hydrocarbon reservoirs, as well as groundwater aquifers. Here, we present outcrop, petrographic and geochemical data for pervasive ferroan dolomite cement bodies up to 250 m in size from Upper Cretaceous Desert Member and Castlegate Sandstone fluvial strata exposed in the Book Cliffs in Utah. These cement bodies are present with coastal plain fluvial strata within both the Desert and Castlegate lowstand sandstones and are most abundant in the thin, distal fluvial strata. Cement bodies are almost entirely absent in updip, thicker, fluvial strata. Petrographic observations suggest a predominantly early diagenetic timing to the mildly ferroan dolomite, with a component of later burial origin. δ13C values for the cement (+4.8 to −5.7‰ V-PDB) suggest a marine-derived source for the earliest phase with a burial organic matter source for later cement. δ18O data (−6.3 to −11.8‰ V-PDB) suggest precipitation from freshwater dominated fluids. It is proposed here that dolomite was derived from leaching of detrital dolomite under lowstand coals and cementation took place in coastal aquifers experiencing mixed meteoric-marine fluids as a result of base-level fluctuations. This data presented here shows that large cement bodies can be an important component within fluvial sandstones with a potentially significant impact upon both reservoir quality and fluid flow within reservoirs, especially at the marine-non-marine interface.  相似文献   

19.
《Marine Geology》1999,153(1-4):199-219
Pyrite formation within and directly below sapropels in the eastern Mediterranean was governed by the relative rates of sulphide production and Fe liberation and supply to the organic-rich layers. At times of relatively high SO2−4 reduction, sulphide could diffuse downward from the sapropel and formed pyrite in underlying sediments. The sources of Fe for pyrite formation comprised detrital Fe and diagenetically liberated Fe(II) from sapropel-underlying sediments. In organic-rich sapropels, input of Fe from the water column via Fe sulphide formation in the water may have been important as well. Rapid pyrite formation at high saturation levels resulted in the formation of framboidal pyrite within the sapropels, whereas below the sapropels slow euhedral pyrite formation at low saturation levels occurred. δ34S values of pyrite are −33‰ to −50‰. Below the sapropels δ34S is lower than within the sapropels, as a result of increased sulphide re-oxidation at times of relatively high sulphide production and concentration when sulphide could escape from the sediment. The percentage of initially formed sulphide that was re-oxidized was estimated from organic carbon fluxes and burial efficiencies in the sediment. It ranges from 34% to 80%, varying significantly between sapropels. Increased palaeoproductivity as well as enhanced preservation contributed to magnified accumulation of organic matter in sapropels.  相似文献   

20.
We report on the isotopic composition of dissolved inorganic carbon (DIC) in pore-water samples recovered by gravity coring from near-bottom sediments at gas hydrate-bearing mud volcanoes/gas flares (Malenky, Peschanka, Peschanka 2, Goloustnoe, and Irkutsk) in the Southern Basin of Lake Baikal. The δ13C values of DIC become heavier with increasing subbottom depth, and vary between ?9.5 and +21.4‰ PDB. Enrichment of DIC in 13C indicates active methane generation in anaerobic environments near the lake bottom. These data confirm our previous assumption that crystallization of carbonates (siderites) in subsurface sediments is a result of methane generation. Types of methanogenesis (microbial methyl-type fermentation versus CO2-reduction) were revealed by determining the offset of δ13C between dissolved CH4 and CO2, and also by using δ13C and δD values of dissolved methane present in the pore waters. Results show that both mechanisms are most likely responsible for methane generation at the investigated locations.  相似文献   

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