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1.
Molecular data from a large set of source rock, crude oil and oil-containing reservoir rock samples from the Tarim Basin demonstrate multiple sources for the marine oils in the studied areas of this basin. Based on gammacerane/C31 hopane and C28/(C27 + C28 + C29) sterane ratios, three of the fifteen crude oils from the Tazhong Uplift correlate with Cambrian-Lower Ordovician source rocks, while the other crude oils from the Tazhong Uplift and all 39 crude oils from the Tahe oilfield in the Tabei Uplift correlate with Middle-Upper Ordovician source rocks. These two ratios further demonstrate that most of the free oils and nearly all of the adsorbed and inclusion oils in oil-containing reservoir rocks from the Tazhong Uplift correlate with Cambrian-Lower Ordovician source rocks, while the free and inclusion oils in oil-containing carbonates from the Tahe oilfield correlate mainly with Middle-Upper Ordovician source rocks. This result suggests that crude oils in the Tazhong Uplift are partly derived from the Cambrian-Lower Ordovician source rocks while those in the Ordovician carbonate reservoirs of Tahe oilfield are overwhelmingly derived from the Middle-Upper Ordovician source rocks.The scatter of C23 tricyclic terpane/(C23 tricyclic terpane + C30 17α,21β(H)-hopane) and C21/(C21 + ΣC29) sterane ratios for the free and inclusion oils from oil-containing carbonates in the Tahe oilfield possibly reflects the subtle organofacies variations in the source rocks, implying that the Ordovician reservoirs in this oilfield are near the major source kitchen. In contrast, the close and positive relationship between these two ratios for oil components in the oil-containing reservoir rocks from the Tazhong Uplift implies that they are far from the major source kitchen.  相似文献   

2.
An Early Permian volcanic assemblage is well exposed in the central-western part of the Apuseni Mountains (Romania). The rocks are represented by rhyolites, basalts and subordinate andesites suggesting a bimodal volcanic activity that is intimately associated with a post-orogenic (Variscan) syn-sedimentary intra-basinal continental molasse sequences. The mafic and mafic-intermediate rocks belong to sub-alkaline tholeiitic series were separated in three groups (I–III) showing a high Th and Pb abundances, depletion in Nb, Ta and Sr, and slightly enriched in LREE patterns (LaN/YbN = 1.4–4.4). Isotopically, the rocks of Group I have the initial ratios 87Sr/86Sr(i) = 0.709351–0.707112, 143Nd/144Nd(i) = 0.512490–0.512588 and high positive ?Nd270 values from 3.9 to 5.80; the rocks of Group II present for the initial ratios values 87Sr/86Sr(i) = 0.709434–0.710092, 143Nd/144Nd(i) = 0.512231–0.512210 and for ?Nd270 the negative values from −1.17 to −1.56; the rocks of Group III display for the initial ratios the values 87Sr/86Sr(i) = 0.710751–0.709448, 143Nd/144Nd(i) = 0.512347–0.512411 and for ?Nd270 the positive values from 1.64 to 2.35. The rocks resembling continental tholeiites, suggest a mantle origin and were further affected by fractionation and crustal contamination. In addition, the REE geochemistry (1 > SmN/YbN < 2.5; 0.9 > LaN/SmN < 2.5) suggests that these rocks were generated by high percentage partial melting of a metasomatized mantle in the garnet peridotite facies. The felsic rocks are enriched in Cs, Rb Th and U and depleted in Nb, Ta, Sr, Eu, and Ti. The REE fractionation patterns show a strong negative Eu anomaly (Eu/Eu* = 0.23–0.40). The felsic rocks show the initial ratios the values: 87Sr/86Sr(i) = 0.704096–0.707805, 143Nd/144Nd(i) = 0.512012–0.512021 and for ?Nd270 the negative values from −5.27 to −5.44. They suggest to be generated within the lower crust during the emplacement of mantle-derived magmas that provided necessary heat to crustal partial melting.  相似文献   

3.
Geochemical characterisation of 18 crude oils from the Potwar Basin (Upper Indus), Pakistan is carried out in this study. Their relative thermal maturities, environment of deposition, source of organic matter (OM) and the extent of biodegradation based on the hydrocarbon (HC) distributions are investigated. A detailed oil-oil correlation of the area is established. Gas chromatography-mass spectrometry (GC-MS) analyses and bulk stable carbon and hydrogen isotopic compositions of saturated and aromatic HC fractions reveals three compositional groups of oils. Most of the oils from the basin are typically generated from shallow marine source rocks. However, group A contains terrigenous OM deposited under highly oxic/fluvio-deltaic conditions reflected by high pristane/phytane (Pr/Ph), C30 diahopane/C29Ts, diahopane/hopane and diasterane/sterane ratios and low dibenzothiophene (DBT)/phenanthrene (P) ratios. The abundance of C19-tricyclic and C24-tetracyclic terpanes are consistent with a predominant terrigenous OM source for group A. Saturated HC biomarker parameters from the rest of the oils show a predominant marine origin, however groups B and C are clearly separated by bulk δ13C and δD and the distributions of the saturated HC fractions supporting variations in source and environment of deposition of their respective source rocks. Moreover, various saturated HC biomarker ratios such as steranes/hopanes, diasteranes/steranes, C23-tricyclic/C30 hopane, C28-tricyclic/C30 hopane, total tricyclic terpanes/hopanes and C31(R + S)/C30 hopane show that two different groups are present. These biomarker ratios show that group B oils are generated from clastic-rich source rocks deposited under more suboxic depositional environments compared to group C oils. Group C oils show a relatively higher input of algal mixed with terrigenous OM, supported by the abundance of extended tricyclic terpanes (up to C41+) and steranes.Biomarker thermal maturity parameters mostly reached to their equilibrium values indicating that the source rocks for Potwar Basin oils must have reached the early to peak oil generation window, while aromatic HC parameters suggest up to late oil window thermal maturity. The extent of biodegradation of the Potwar Basin oils is determined using various saturated HC parameters and variations in bulk properties such as API gravity. Groups A and C oils are not biodegraded and show mature HC profiles, while some of the oils from group B show minor levels of biodegradation consistent with high Pr/n-C17, Ph/n-C18 and low API gravities.  相似文献   

4.
Hydrous pyrolysis (HP) experiments were used to investigate the petroleum composition and quality of petroleum generated from a Brazilian lacustrine source rock containing Type I kerogen with increasing thermal maturity. The tested sample was of Aptian age from the Araripe Basin (NE-Brazil). The temperatures (280–360 °C) and times (12–132 h) employed in the experiments simulated petroleum generation and expulsion (i.e., oil window) prior to secondary gas generation from the cracking of oil. Results show that similar to other oil prone source rocks, kerogen initially decomposes in part to a polar rich bitumen, which decomposes in part to hydrocarbon rich oil. These two overall reactions overlap with one another and have been recognized in oil shale retorting and natural petroleum generation. During bitumen decomposition to oil, some of the bitumen is converted to pyrobitumen, which results in an increase in the apparent kerogen (i.e., insoluble carbon) content with increasing maturation.The petroleum composition and its quality (i.e., API gravity, gas/oil ratio, C15+ fractions, alkane distribution, and sulfur content) are affected by thermal maturation within the oil window. API gravity, C15+ fractions and gas/oil ratios generated by HP are similar to those of natural petroleum considered to be sourced from similar Brazilian lacustrine source rocks with Type I kerogen of Lower Cretaceous age. API gravity of the HP expelled oils shows a complex relationship with increasing thermal maturation that is most influenced by the expulsion of asphaltenes. C15+ fractions (i.e., saturates, aromatics, resins and asphaltenes) show that expelled oils and bitumen are compositionally separate organic phases with no overlap in composition. Gas/oil ratios (GOR) initially decrease from 508–131 m3/m3 during bitumen generation and remain essentially constant (81–84 m3/m3) to the end of oil generation. This constancy in GOR is different from the continuous increase through the oil window observed in anhydrous pyrolysis experiments. Alkane distributions of the HP expelled oils are similar to those of natural crude oils considered to be sourced from similar Brazilian lacustrine source rocks with Type I kerogen of Lower Cretaceous age. Isoprenoid and n-alkane ratios (i.e., pristane/n-C17 and phytane/n-C18) decrease with increasing thermal maturity as observed in natural crude oils. Pristane/phytane ratios remain constant with increasing thermal maturity through the oil window, with ratios being slightly higher in the expelled oils relative to those in the bitumen. Generated hydrocarbon gases are similar to natural gases associated with crude oils considered to be sourced from similar Brazilian lacustrine source rocks with Type I kerogen of Lower Cretaceous, with the exception of elevated ethane contents. The general overall agreement in composition of natural and hydrous pyrolysis petroleum of lacustrine source rocks observed in this study supports the utility of HP to better characterize petroleum systems and the effects of maturation and expulsion on petroleum composition and quality.  相似文献   

5.
The Masila Basin is an important hydrocarbon province in Yemen, but the origin of hydrocarbons and their generation history are not fully understood. In this regard, 10 crude oils from different petroleum reservoir sections in the Masila Basin were characterized by a variety of biomarker and non-biomarker parameters using GC, GC-MS and stable carbon isotope techniques. Oils from the Masila Basin display pristane/phytane (Pr/Ph) ratios ranging from 1.7 to 2.0, low sulfur content, high C35 homohopane index, relatively high C27 sterane concentrations and relatively high tricyclic terpanes suggesting a marine clay source rock that was deposited in mildly anoxic to suboxic conditions with dominantly algal organic matter. C29 20S/(20S + 20R) steranes and ββ/(ββ + αα) sterane ratios indicate that the Masila oils have reached peak oil window maturity. Another related feature of these oils is the absence of 18α (H)-oleanane, which suggests a source age older than Cretaceous. The carbon isotope compositions are similar to those of the potential source rocks, which range from −25.4‰ to −28.3‰, indicating a marine environment. The new data presented in this paper suggest that the Masila oils constitute one oil family and that the oil originated from the Upper Jurassic Madbi source rock in the basin.  相似文献   

6.
On the basis of the results of hydropyrolysis simulations for about 90 different types of immature to mature source rocks selected from about 5 000 marine source rocks in China, along with the natural thermal evolution profiles, the following conclusions were obtained. (1) Total organic carbon (TOC) content of excellent marine source rocks does not change obviously when Ro < 0.8% or Ro > 1.3%, and the residual TOC content is decreasing gradually with the maturity increase at 0.8% < Ro < 1.3%. (2) At the high-post mature stage (Ro > 1.3%), the decreased maximums of residual TOC content for the kerogen of sapropel (I), II1, and II are usually 40%, 32% and 24%, respectively, and their TOC restitution coefficient is, respectively, 1.68, 1.48 and 1.32. (3) Both the TOC decreasing amplitude and the restitution coefficient decrease gradually with the decrease of TOC content for the source rocks with low organic matter abundance (usually 0.3% < TOC < 1.0%). The TOC restitution coefficients are, respectively, 1.20 and 1.0, when 0.3% < TOC < 0.5% and TOC < 0.3%. (4) TOCres of solid bitumen and shale with high organic matter abundance (TOC > 30%) also require no restitution at the high mature stage. Such kind of TOC restitution is further supported by the coincidence of the decrease of residual TOC with the decreasing of S1 + S2 and the increasing of hydrocarbon quantity during the experimental simulation of hydrocarbon generation and expulsion for marine source rocks (0.3% < TOC < 30%) in natural thermal evolution profiles. __________ Translated from Earth Science—Journal of China University of Geosciences, 2007, 32(6): 853–860 [译自: 地球科学—中国地质大学学报]  相似文献   

7.
1-Alkyl-2,3,6-trimethylbenzenes and a high relative amount of 1,2,3,4-tetramethylbenzene (TTMB) have been previously detected in the marine oils and asphaltenes in the oils from the Tarim Basin. In the present study, the stable carbon isotopic compositions of TTMB and n-alkanes in the pyrolysates of asphaltenes in the marine oils from the northern Tarim Basin and Silurian tar sands from the Tarim Basin were determined. TTMB has stable carbon isotopic compositions in the range from −23‰ to −24‰ and are about 12‰ more enriched in 13C than concomitant n-alkanes (−35‰ to −37‰) in the pyrolysates. The results indicate a contribution from green sulfur bacteria (Chlorobiaceae) to TTMB. Thus, the depositional environments of the source rocks for the marine oils and the bitumen in tar sands from the Tarim Basin are characterized by periods of euxinic conditions within the photic zone.  相似文献   

8.
The Xiong’er Group is an important geologic unit in the southern margin of the North China Craton. It is dominated by the volcanic rocks, dated at 1763 ± 15 Ma, that have SiO2 contents ranging from 52.10 wt% to 73.51 wt%. These volcanic rocks are sub-alkaline and can be classified into three subgroups: basaltic andesites, andesites and rhyolites. They unexceptionally show enrichment of light rare earth elements (LREE) and share similar trace element patterns. Depletions in Nb, Ta, Sr, P and Ti relative to the adjacent elements are evident for all the samples. The volcanic rocks are evolved with low MgO contents (0.29–5.88 wt%) and accordingly low Mg# values of 11–53. The Nd isotopes are enriched and show a weak variation with ?Nd(t) = −7.12 to −9.63. Zircon Hf isotopes are also enriched with ?Hf(t) = −12.02 ± 0.45. The volcanic rocks of the Xiong’er Group are interpreted to represent fractional crystallization of a common mantle source. The volcanic rocks might have been generated by high-degree partial melting of a lithospheric mantle that was originally modified by the oceanic subduction in the Late Archean. This brings a correlation with the subduction-modified lithospheric mantle in an extensional setting during breakup of the Columbia supercontinent in the late Paleoproterozoic, rather than in an arc setting. The elevated SiO2 contents and evolved radiogenic isotope features indicate the possible incorporation into their source of lower crustal materials that have similar Nd isotopic characteristics to the subcontinental lithospheric mantle. The existence of extensive Xiong’er volcanic rocks (60,000 km2) indicates an early large-scale subduction-related metasomatism in the area and probably suggest a flat subduction model for the plate-margin magmatism in the Late Archean.  相似文献   

9.
《Applied Geochemistry》2005,20(10):1875-1889
Based on the systematic analyses of light hydrocarbon, saturate, aromatic fractions and C isotopes of over 40 oil samples along with related Tertiary source rocks collected from the western Qaidam basin, the geochemical characteristics of the Tertiary saline lacustrine oils in this region was investigated. The oils are characterized by bimodal n-alkane distributions with odd-to-even (C11–C17) and even-to-odd (C18–C28) predominance, low Pr/Ph (mostly lower than 0.6), high concentration of gammacerane, C35 hopane and methylated MTTCs, reflecting the high salinity and anoxic setting typical of a saline lacustrine depositional environment. Mango’s K1 values in the saline oils are highly variable (0.99–1.63), and could be associated with the facies-dependent parameters such as Pr/Ph and gammacerane indexes. Compared with other Tertiary oils, the studied Tertiary saline oils are marked by enhanced C28 sterane abundance (30% or more of C27–C29 homologues), possibly derived from halophilic algae. It is noted that the geochemical parameters of the oils in various oilfields exhibit regular spatial changes, which are consistent with the depositional phase variations of the source rocks. The oils have uncommon heavy C isotopic ratios (−24‰ to −26‰) and a flat shape of the individual n-alkane isotope profile, and show isotopic characteristics similar to marine organic matter. The appearance of oleanane and high 24/(24 + 27)-norcholestane ratios (0.57–0.87) in the saline oils and source rocks confirm a Tertiary organic source.  相似文献   

10.
Chemical (meta)sedimentary rocks in the amphibolite facies ≥3700 Ma Isua supracrustal belt (W. Greenland) are mostly strongly deformed, so there is only a small chance of the survival of features such as stromatolites or microfossils that would be direct proof of a ≥3700 Ma biosphere. Therefore the search for evidence of ≥3700 Ma life in Isua rocks has focused on chemical signatures, particularly C-isotopes. The new approach presented here is based on whole rock chemistry rather than isotopic signatures. Isua chemical sedimentary rocks have Ca–Mg–Fe bulk compositions that coincide with ferroan dolomite – siderite/Fe-oxide mixtures. Most have low Al2O3, TiO2 contents (<0.5 and <0.05 wt% respectively) showing minimal contamination from terriginous materials. Identical seawater-like REE + Y shale-normalised trace element signatures with La, Ce, Eu and Y positive anomalies are found in magnetite-rich banded iron formation (BIF – such as the geochemical standard IF-G), dolomite-rich rocks and quartz–carbonate–calc-silicate rocks. Additionally from a rare, small area of low deformation in Isua, there are ∼3700 Ma pillow lava interstices consisting of quartz + tremolite + calcite derived from pre-metamorphic dolomite + silica. Thus the dolomite in the chemical sediments and the pillow interstice was part of the pre-metamorphic assemblage, and was deposited from seawater and/or low-temperature groundwater (as shown by the REE + Y chemistry). Therefore, at least some Isua carbonate rocks are sedimentary or diagenetic in origin rather than being formed by metasomatism at 600–500 °C as proposed by Rose et al. (1996. American Journal of Science 296, 1004–1044).  相似文献   

11.
对北黄海盆地LV井中、上侏罗统烃源岩及上侏罗统原油（油砂抽提物）进行常规有机地球化学分析和碳同位素测试,分析研究烃源岩和原油的地球化学特征并探讨原油的来源问题。测试结果显示,侏罗系烃源岩达成熟-高熟阶段,有机质类型以Ⅲ型为主。中侏罗统烃源岩有机碳含量较高,但生烃潜能、氯仿沥青“A”及总烃含量低值,属于差的烃源岩。干酪根碳同位素总体偏重（-24.4‰～-23.5‰）,与原油碳同位素特征（-29‰左右）差异显著,排除与原油的母岩关系。上侏罗统烃源岩有机碳含量较中侏罗统低,但生烃潜能、氯仿沥青“A”及总烃含量高值。上侏罗统烃源岩抽提氯仿沥青“A”碳同位素（-26‰～-21.5‰）特征、单体烃碳同位素分布模式及甾萜烷生物标志物特征都与原油相似,综合分析认为原油应该来源于上侏罗统中干酪根类型较好、母质为混源的成熟烃源岩。  相似文献   

12.
Four crude oil samples from the Sergipe–Alagoas Basin, northeastern Brazil, were analyzed using full scan gas chromatography–quadrupole mass spectrometry (GC–qMS) for biomarkers, in order to correlate them using aromatic carotenoids thereby enhancing knowledge about the depositional environment of their source rocks. The geochemical parameters derived from saturated fractions of the oils show evidence of little or no biodegradation and similar thermal maturation (Ts/(Ts + Tm) for terpanes, C29 αββ/(αββ + ααα), C27, and C29 20S/(20S + 20R) for steranes). Low pristane/phytane ratios and the abundance of gammacerane and β-carotane are indicative of an anoxic and saline depositional environment for the source rocks. Moreover, we identified a large range of diagenetic and catagenetic products of the aromatic carotenoid isorenieratene, including C40, C33, and C32 diaryl isoprenoids and aryl isoprenoid derivatives with short side chains and/or additional rings. These results indicate anoxia in the photic zone during the deposition of the source rocks.  相似文献   

13.
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.  相似文献   

14.
Here we present the first set of metal-silicate partitioning data for Cs, which we use to examine whether the primitive mantle depletion of Cs can be attributed to core segregation. Our experiments independently varied pressure from 5 to 15 GPa, temperature from 1900 to 2400 °C, metallic sulfur content from pure Fe to pure FeS, silicate melt polymerization, expressed as a ratio of non-bridging oxygens to tetrahedrally coordinated cations (nbo/t) from 1.26 to 3.1, and fO2 from two to four log units below the iron-wüstite buffer. The most important controls on the partitioning behavior of alkalis were the metallic sulfur content, expressed as XS, and the nbo/t of the silicate liquid. Normalization of XS to 0.5 yielded the following expressions for D-values as a function of nbo/t: log DNa = −2.0 + 0.44 × (nbo/t), log DK = −2.4 + 0.67 × ( nbo/t), and log DCs = −3.2 + 1.17 × (nbo/t). Normalization of nbo/t to 2.7 resulted in the following equations for D-values as a function of S content: log DNa = −4.1 + 6.4 × XS, log DK = −7.7 + 13.9 × XS, and log DCs = −12.1 + 23.3 × XS.There appears to be a negative pressure effect up to 15 GPa, but it should be noted that this trend was not present before normalization, and is based on only two measurements. There is a positive trend in cesium’s metal-silicate partition coefficient with increasing temperature. DCs exhibits the largest change and increased by a factor of three over 500 °C. The effect of oxygen fugacity has not been precisely determined but in general, lowering fO2 by two log units resulted in a rise in all D-values of approximately an order of magnitude. In general, the sensitivity of partition coefficients to changing parameters increased with atomic number.The highest D-value for Cs observed in this study is 0.345, which was obtained at nbo/t of 2.7 and a metal phase of pure FeS. This metallic composition has far more S than has been suggested for any credible core-forming metal. We therefore conclude that the depletion of Cs in Earth’s mantle is either caused by radically different behavior of Cs at pressures higher than 15 GPa or is not related to core formation. Even so, we have shown that a planet with a sufficient S inventory may incorporate significant amounts of alkali elements into its core.  相似文献   

15.
Reports of the high ion content of steam and low-density supercritical fluids date back to the work of Carlon [Carlon H. R. (1980) Ion content of air humidified by boiling water.J. Appl.Phys.51, 171-173], who invoked ion and neutral-water clustering as mechanism to explain why ions partition into the low-density aqueous phase. Mass spectrometric, vibrational spectroscopic measurements and quantum chemical calculations have refined this concept by proposing strongly bound ion-solvent aggregates and water clusters such as Eigen- and Zundel-type proton clusters H3O+·(H2O)m and the more weakly bound water oligomers (H2O)m. The extent to which these clusters affect fluid chemistry is determined by their abundance, however, little is known regarding the stability of such moieties in natural low-density high-temperature fluids. Here we report results from quantum chemical calculations using chemical-accuracy multi-level G3 (Curtiss-Pople) and CBS-Q theory (Peterson) to address this question. In particular, we have investigated the cluster structures and clustering equilibria for the ions and H3S+·(H2O)m(H2S)n, where m ? 6 and n ? 4, at 300-1000 K and 1 bar as well as under vapor-liquid equilibrium conditions between 300 and 646 K. We find that incremental hydration enthalpies and entropies derived from van’t Hoff analyses for the attachment of H2O and H2S onto H3O+, and H3S+ are in excellent agreement with experimental values and that the addition of water to all three ions is energetically more favorable than solvation by H2S. As clusters grow in size, the energetic trends of cluster hydration begin to reflect those for bulk H2O liquids, i.e. calculated hydration enthalpies and entropies approach values characteristic of the condensation of bulk water (ΔHo = −44.0 kJ mol−1, ΔSo = −118.8 J K mol−1). Water and hydrogen sulfide cluster calculations at higher temperatures indicate that a significant fraction of H3O+, and H3S+ ions exists as solvated moieties.  相似文献   

16.
The geochemistry of Quaternary volcanic rocks from Datong provides important constraints on the petrogenesis of continental alkali and tholeiitic basalts and lithospheric evolution in the western North China Craton. Alkali basalts in north Datong have trace element compositions similar to oceanic island basalts (OIB). They show nearly homogenous isotopic compositions (?Nd = 5.4-6.8 and 87Sr / 86Sr = 0.7035-0.7037) that resemble the nearby Hannuoba Miocene basalts, indicating that the two lava suites share a similar asthenospheric source. However, Datong basalts have conspicuously lower Al2O3 and CaO, higher SiO2 and HREE contents and Na / Ti ratios, compared to Hannuoba lavas at comparable MgO. This compositional difference is attributable to the combined effect of source difference and temporal decrease in melting depth. The latter reflects Cenozoic lithospheric thinning of the western North China Craton.Tholeiitic basalts in southeast Datong have incompatible element ratios that differ from OIB; they have lower ?Nd (1.3-3.7) and higher 87Sr / 86Sr (0.7039-0.7046) compared to alkali basalts. These moderately evolved rocks (MgO < 7%) display unusually high Cr concentrations (> 200 ppm), a nearly flat LREE pattern and a fractionated HREE with the “kink” occurring at Gd. A shallow melting depth (< 60 km), suggested by their Q-normative composition, is in conflict with the residual garnet in the source (> 75 km) as required by REE modeling. This paradox, which is reminiscent of that for Hawaiian tholeiites, can be reconciled if garnet lherzolite melts react with refractory peridotites during which orthopyroxene is dissolved and olivine precipitates. The diagnostic consequence of this melt-rock reaction includes increases in SiO2 and Cr, decreases in Al2O3 and CaO, and formation of “kinked” REE patterns. Involvement of lithospheric mantle in the genesis of Datong tholeiites may be related to the Cenozoic lithospheric thinning/erosion in the western North China Craton. The spatial distribution of Datong alkali and tholeiitic basalts may be related to enhanced extension along the lithospheric boundary between the Western Block of the North China Craton and the Trans-North China Orogen.  相似文献   

17.
The major, trace and rare earth element (REE) contents of metapelite (MPL), metapsammite (MPS) and metamarl (MM) samples from the Cambro-Ordovician Seydi?ehir Formation were analyzed to investigate their provenance and tectonic setting. The MPS, MPL, and MM samples have variable SiO2 concentrations, with average values of 72.36, 55.54, and 20.95 wt%, moderate SiO2/Al2O3 ratios (means of 6.88, 3.23, and 3.80), moderate to high Fe2O3 + MgO contents (means of 5.14, 9.55, 3.56 wt%), and high K2O/Na2O ratios (means of 3.26, 3.64, 2.90), respectively. On average, the chemical index of alteration (CIA) values of the MPS and the MPL are 65.87 and 71.96, respectively, while the chemical index of weathering (CIW) values are 74.54 and 85.09, respectively. These data record an intermediate to high degree of alteration (weathering) of plagioclase to illite/kaolinite in the samples’ provenance. The chondrite-normalized REE patterns of all the sample groups are similar and are characterized by subparallel light rare earth elements (LREE)-enriched, relatively flat heavy rare earth elements (HREE) patterns with pronounced Eu anomalies (mean of 0.69) and moderate fractionation [average (La/Yb)N = 8.7]. Plots of sediments in ternary diagrams of La, Th, Sc and elemental ratios (La/Sc, Th/Sc, Cr/Th, Eu/Eu*, La/Lu, Co/Th, La/Sc and Sc/Th), which are critical for determining provenance, and REE patterns indicate that the metaclastic units of the Seydi?ehir Formation were derived dominantly from felsic to intermediate magmatic rocks and not from a mafic source. The La–Sc–Th and Th–Sc–Zr/10 ternary diagrams of the Seydi?ehir Formation are typical of continental island arc/active continental margin tectonic settings. The geologic location and geochemistry of the Seydi?ehir Formation suggest that it was deposited in an Andean-type retroarc foreland basin during the Late Cambrian–Early Ordovician period. The Neoproterozoic intermediate to felsic magmatic rocks and metaclastic sediments with felsic origins of the Sand?kl?–Afyon Basement Complex (SBC) and their equivalent units, which are thought to be overlain by the younger units in the study area, may be the dominant source rocks for the Seydi?ehir Formation.  相似文献   

18.
Organic geochemical characterization of cutting samples from the Abu Hammad-1 and Matariya-1 wells elucidates the depositional environment and source rock potential of the Jurassic and Lower Cretaceous successions and the Middle Miocene to Pleistocene section in the southern and eastern Nile Delta Basin. The burial and thermal histories of the Mesozoic and Miocene sections were modeled using 1D basin modeling based on input data from the two wells. This study reveals fair to good gas-prone source rocks within the Upper Jurassic and Lower Cretaceous sections with total organic carbon (TOC) averaging 2.7% and hydrogen index (HI) up to 130 mg HC/g TOC. The pristane/n-C17 versus phytane/n-C18 correlation suggests mixed marine and terrestrial organic matter with predominant marine input. Burial and thermal history modeling reveals low thermal maturity due to low heat flow and thin overburden. These source rocks can generate gas in the western and northern parts of the basin where they are situated at deeper settings. In contrast, the thick Middle Miocene shows fair source rock quality (TOC averaging at 1.4%; HI maximizing at 183 mg HC/g TOC). The quality decreases towards the younger section where terrestrial organic matter is abundant. This section is similar to previously studied intervals in the eastern Nile Delta Basin but differs from equivalents in the central parts where the quality is better. Based on 1D modeling, the thick Middle Miocene source rocks just reached the oil generation stage, but microbial gas, however, is possible.  相似文献   

19.
Geochemical variations in stream sediments (n = 54) from the Mahaweli River of Sri Lanka have been evaluated from the viewpoints of lithological control, sorting, heavy mineral concentration, influence of climatic zonation (wet, intermediate, and dry zones), weathering, and downstream transport. Compositions of soils (n = 22) and basement rocks (n = 38) of the catchment and those of <180 μm and 180–2000 μm fractions of the stream sediments were also examined. The sediments, fractions, soils and basement rocks were analyzed by X-ray fluorescence to determine their As, Pb, Zn, Cu, Ni, Cr, V, Sr, Y, Nb, Zr, Th, Sc, Fe2O3, TiO2, MnO, CaO, P2O5 and total sulfur contents. Abundances of high field strength and ferromagnesian elements in the sediments indicate concentration of durable heavy minerals including zircon, tourmaline, rutile, monazite, garnet, pyriboles, and titanite, especially in <180 μm fractions. The sediments show strong correlation between Ti and Fe, further suggesting presence of heavy mineral phases containing both elements, such as ilmenite and magnetite. The basement rocks range from mafic through to felsic compositions, as do the soils. The river sediments lack ultrabasic components, and overall have intermediate to felsic compositions. Elemental spikes in the confluences of tributary rivers and high values in the <180 μm fractions indicate sporadic inputs of mafic detritus and/or heavy minerals to the main channel. Al2O3/(K2O + Na2O) and K2O/Na2O ratios of the sediments and LOI values of the soils correlate well with the climatic zones, suggesting intense weathering in the wet zone, lesser weathering in the intermediate zone, and least weathering in the dry zone. Low Sr and CaO contents and Cr/V ratios in stream sediments in the wet zone also suggest climatic influence. Fe-normalized enrichment factors (EFs) for As, Pb, Zn, Cu, Ni and Cr in stream sediments in the main channel are nearly all <1.5, indicating there is no significant environmental contamination. The chemistry of the sediments, rocks and the soils in the Mahaweli River are thus mainly controlled by source lithotype, weathering, sorting, and heavy mineral accumulation.  相似文献   

20.
The evolution of fluorescence has been measured for “live” oils generated from 14 oil-prone kerogens or coals from varying depositional environments during closed system pyrolysis in a diamond anvil cell at three heating rates (3, 8, and 25 °C/min), and temperatures up to 600 °C. The measured fluorescence intensities of the samples, employing using violet excitation at 405 nm, increases significantly during maturation intervals within the oil window, while the fluorescence spectra of oils generated from all studied kerogens exhibit progressive blue-shift of peak wavelengths (λmax) and red/green quotients (I650/I500) upon increasing maturity. The observed trend is consistent with a maturity dependence of the spectral shift, which is widely recognized in natural hydrocarbon inclusions and crude oils using ultraviolet (UV) excitation (365 nm). The data presented herein suggest that the λmax of spectra for inclusion oils shift in similar direction despite differences in composition or source kerogen. This implies that the reverse or anomalous trends reported for inclusion oils in nature may be attributed to other processes, which significantly alters the fluorescence properties of oils subsequent to their generation. Oils with the similar color (λmax or I650/I500) can be derived from diverse kerogens with maturities that vary by ±0.3% Ro, suggesting that the fluorescent colors of crude and inclusion oils are both maturity- and source-dependent, and therefore cannot be used as universal maturity indicators. In addition, the blue-shifts observed for cumulative oils generated from all kerogens approaches similar minima λmax values around the green-yellow wavelength (564 nm) and at I650/I500 values around 0.6, at maturities close to the middle or late stage of oil generation. This suggests that most late-stage cumulative oils will exhibit similar colors. Oils generated during late-stage maturity intervals, however, can exhibit colors with shorter wavelengths.  相似文献   

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