Illitic clay is ubiquitous in clastic hydrocarbon reservoirs, and the host for several radiometric isotopes such as the potassium-argon (K-Ar) and rubidium-strontium (Rb-Sr) systems. This study applied the isotope-dilution thermal ionization mass spectrometry technique for small samples (3–4 mg) to conduct illite Rb-Sr isotope dating of five illitic clay samples from the Silurian bituminous sandstone (SBS) intersected by five drillholes in the Tarim Basin, NW China. The 87Rb/86Sr ratio of clays is fractionated mainly by the addition of Rb during the illitization of mixed-layer illite/smectite (I/S), which is the dominant clay species in the Tarim Basin samples. The subsample-scale Rb/Sr isotope values suggest that each subsample may contain I/S particles of slightly variable degrees of illitization. Three of the analyzed samples (H6, KQ1 and TZ67) generated Rb-Sr isochron ages of 141 ± 61 Ma, 332 ± 32 Ma and 235 ± 8 Ma (errors quoted at 2σ), respectively. These results are similar to the corresponding K-Ar ages (125 Ma, 389 Ma and 234 Ma). The isotopic ages are consistent with the timing of hydrocarbon charge which varies in different drillholes as constrained by basin modelling, indicating that a closed-system behavior is attained by the hydrocarbon charge that inhibits the illitization of I/S. The Rb-Sr isotope analyses of the other two samples (YM35-1 and Q1) that did not yield isochron ages suggest the conditions for producing isochrons were not satisfied, which may be caused by disturbance of the isotope system by a post-charge hydrothermal event. The outcomes of this study show the robust potential of Rb-Sr clay subsample geochronology for cross-checking isotopic ages yielded by other systems (e.g. K-Ar system) and constraining the timing of hydrocarbon charge.
In a hydrocarbon system, knowledge of the timing of the hydrocarbon charge is crucial for understanding its evolution. Emplacement of hydrocarbon in a porous reservoir alters its chemical condition and affects mineral diagenesis1,2,3,4,5. Authigenic illitic clay commonly occurs in hydrocarbon reservoirs and its diagenesis is sensitive to fluid flow1,5. Several long-lived radiometric isotope systems, including potassium-argon (K-Ar) and rubidium-strontium (Rb-Sr), are hosted in illitic clay, and these isotope systems can document the timing of clay diagenesis and constrain fluid flow history3,6,7,8,9,10. Closed system behavior of isotope systems in illitic clays is related to its diagenesis6. Illitic clay diagenesis requires appropriate temperature conditions (e.g. >60 °C)8 and the availability of sufficient potassium6. The illitization process may cease if either condition is not satisfied6. The isotopic systems (e.g. Rb-Sr and K-Ar) in illitic clays remain closed if illitization ceases because there is no K/Ar or Rb/Sr exchange between the mineral and external environment6.
Potassium-Ar clay geochronology has been proven a useful tool for investigating fluid flow in depositional basins3,5,10. The K-Ar method is based on the β+ decay of 40K to 40Ar11, and an isotopic age is acquired through separate measurements of K and Ar on two aliquots of a single sample12. The 40Ar-39Ar method is a variant for the K-Ar method, with an additional irradiation pre-treatment of samples, where 39K is transformed into 39Ar by fast neutrons12. Although the 40Ar-39Ar method has recognized practical analytical improvement compared to the K-Ar method, e.g. simultaneous analysis of radioactive and radiogenic atoms on the same aliquot, which prevents uncertainties induced by sample heterogeneity12, the 39Ar recoil associated with the irradiation procedure may result in spurious age data for micrometer-size clay minerals13,14,15.
The Rb-Sr isotope system is another applicable geochronometer for illitic clays. The isochron age is yielded through the regression of Rb-Sr isotope data obtained generally by either bulk analysis or the acid-leaching technique10,16,17,18. The age yielded by bulk analysis represents an average estimate of a suite of cogenetic samples, instead of a single sample, thus may be unfavorable for precious samples (e.g. petroleum drillcore). Rb-Sr analysis of different acid leaching fractions of a sample may yield an isochron age for the single sample because Sr is more leachable than Rb, thus generating Rb/Sr fractionation between leachate and residue10,19,20. However, ions at leachable sites may be susceptible to geo-fluid flows and Sr isotopic heterogeneity may occur between different leaching fractions, resulting in spurious ages7.
Owing to the development of the low-blank Rb/Sr chemistry procedure and high-sensitivity isotope-dilution thermal ionization mass spectrometry (ID-TIMS)21,22, it becomes achievable to determine the Rb-Sr isotopic composition for illitic clays in small quantities (3–4 mg). Therefore, an isochron may be established for a single clay sample through Rb-Sr analysis of multiple extractions from the same sample (i.e. “subsamples”) without additional experimental leaching steps. The aim of this study is to illustrate the feasibility of this dating method through cross-checking against K-Ar ages for the samples initially reported in ref.13.
Silurian bituminous sandstone (SBS) is a significant hydrocarbon reservoir in the Tarim Basin, northwest (NW) China. In recent years, a series of K-Ar clay geochronology studies of this target have been reported, showing that clay diagenesis in the SBS is related to the hydrocarbon charge5,13,23,24,25,26. In this paper, subsample Rb-Sr data for five SBS clay samples are presented. These samples have been characterized in terms of mineralogy and K-Ar geochronology in ref.13.
The Tarim Basin is a large petroliferous basin in NW China (Fig. 1A), covering an area of ~5.6 × 105 km2 27,28,29,30,31. The basin is divided into eleven units, including six depressions (Manjiaer, Kuqa, Awati, Tangguzibasi, Southwestern and Southeastern) and five uplifts (Tadong, Tabei, Tazhong, Bachu and Tanan) (Fig. 1B)28,32. Multiple Phanerozoic tectonic events, related to global episodes, including Caledonian (Ordovician–Devonian), Hercynian (Carboniferous–Permian), Indosinian (Triassic), Yanshanian (Jurassic–Cretaceous) and Himalayan movements (Paleogene–Quaternary), have affected the basin (Fig. 2)30,31, that is filled with Paleozoic-Cenozoic sediments (Fig. 2)28,30. Cambrian–Ordovician carbonate rocks and Silurian–Devonian clastic rocks were deposited in a marine environment (Fig. 2)27,30,33,34,35. A Carboniferous-Permian transitional basin was formed subsequently, after which continental clastic sediments were deposited during the Mesozoic to Cenozoic (Fig. 2)28,30,35.
Lower Silurian sandstone is a significant hydrocarbon reservoir in the Tarim Basin and accommodates abundant solid bitumen, and thus the reservoir is also named the Silurian bituminous sandstone (SBS)5,36. Hydrocarbons in the SBS have marine molecular and stable isotopic compositions and show genetic affinity to the underlying Cambrian-Ordovician source rocks36. The SBS is mainly distributed in the area surrounding the Manjiaer and Awati depressions36. Illite K-Ar geochronology shows that the timing of hydrocarbon charge in the SBS varies locally, owing to variation in the timing of hydrocarbon generation5,13.
Sample Information and Analytical Method
The samples used in this study were 0.3–0.15 μm fractions of five clay samples utilized in the study of ref.13. The five illitic clay samples were separated from sandstone drillcores YM35-1, H6, KQ1, Q1 and TZ67 (Fig. 1B), using the method described in ref.13. Grain size fractions (<0.15, 0.15–0.3, 0.3–0.5 and 0.5–1.0 μm) were separated in distilled water using a progressive high-speed ultra-centrifuge13. The 0.3–0.15 μm fraction was selected for the Rb-Sr isotopic study based on the following considerations: (1) detrital minerals are generally coarser in size, whereas they may be mixed in the 0.5–0.3 and 1–0.5 μm size fractions5,9; (2) the finest fraction (<0.15 μm) may also contain inherited 87Sr atoms of detrital origin37,38. Thus, the 0.3–0.15 μm size fraction is the most appropriate for this study. Scanning electron microscopic (SEM) and X-ray powder diffraction (XRD) investigations by ref.13 also confirmed the purity and authigenic origin of this size fraction. Ordered mixed layer illite/smectite (I/S) is the dominant species in all these samples with no detrital K-feldspar or illite identified13. Sample information, mineralogical information and K-Ar dating results and are listed in Table 1 and Figs 3 and 4.
The Rb-Sr chemistry and mass spectrometry analyses were completed at the State Key Laboratory of Lithospheric Evolution, Institute of Geology and Geophysics, Chinese Academy of Sciences (IGGCAS), Beijing. Five portions of each sample were randomly picked and each subsample was weighed so that 3–4 mg was obtained using an AG104 Mettler Toledo analytical balance. They were then dissolved with 87Rb-84Sr isotopic tracers in 0.1 mL HF (22N) and 0.03 mL HNO3 (14N) in screw-top PFA Savillex vials. The Rb and Sr fractions were separated and purified via a mini-column containing ~30 μL of Sr Spec resin21. Isotope ratios for Rb and Sr were determined using a multi-collector Triton plus TIMS instrument21,22. 87Sr/86Sr ratios were normalized to 88Sr/86Sr = 8.375209 using the exponential law. Duplicate analyses of Sr standard NBS987 during this study yielded a mean 87Sr/86Sr value of 0.710244 ± 0.000012 (2σ, n = 4) in good agreement with the reported value of 0.710251 ± 0.00001621. Analytical uncertainties for 87Rb/86Sr ratios were less than 1%. The blank during the analytical session was lower than 3 pg for Rb and 6 pg for Sr. The Rb-Sr isochron ages for samples were calculated using the ISOPLOT3.0 software39, applying a decay constant (λ87Rb) of 1.396 × 10-11 yr−1 40. Acids used during the Rb-Sr chemistry were all analytical reagent (AR) grade and were purified utilizing a SavillexTM DST-1000 sub-boiling distillation system. Ultrapure water with resistivity of 18.2 MΩ cm−1 obtained from a Milli-Q Element system was used throughout this work. Errors of 87Rb/86Sr ratios are 1% (2σ).
YM35-1: Subsample A-3 has 87Sr/86Sr higher than the other subsamples (Table 2), and is not included in the calculations. The regression of the remaining four subsamples yields an isochron age of 111 ± 36 Ma (2σ, Fig. 6A). There is no obvious relation between 87Sr/86Sr and 1/Sr (Fig. 7A).
H6: Regression of the isotope data yields an isochron age of 148 ± 68 Ma (2σ, Fig. 6B). One subsample (B-4) slightly deviates from the isochron, and the regression without this point yields an identical age within uncertainty (141 ± 61 Ma, 2σ, Fig. 6B). Initial 87Sr/86Sr (Sri) values of the two regressions also overlap within uncertainty (0.7137 ± 0.0069 and 0.7145 ± 0.0062, respectively, Fig. 6B). There is no relation between 87Sr/86Sr and 1/Sr, indicating that the isochrons are not mixing lines (Fig. 7B).
KQ1: Regression of Rb-Sr data for the five subsamples yields an isochron age of 351 ± 97 Ma and Sri of 0.7116 ± 0.0064 (2σ, Fig. 6C). One point slightly deviates from the main trend (C-5, Fig. 6C), and the regression without this point yields a similar isochron age of 332 ± 32 Ma and Sri of 0.7127 ± 0.0021 (2σ, Fig. 6C). There is no relation between 87Sr/86Sr and 1/Sr, indicating that the isochrons are not mixing lines (Fig. 7C).
Q1: Regression of all Rb-Sr data yields an age of 484 ± 51 Ma and a Sri of 0.6972 ± 0.0082 (2σ, Fig. 6D). A linear trend with a steeper slope is defined by the Rb-Sr isotope data of three subsamples (D-1, D-4 and D-5, Fig. 6D). The linear relation between 1/Sr and 87Sr/86Sr for the three subsamples suggests that this three-point “isochron” is a mixing line (Fig. 7D).
TZ67: Regression of Rb-Sr data yields a precise isochron age of 235 ± 8 Ma (2σ) with the Sri of 0.71011 ± 0.00048 (Fig. 6E). There is no relation between 87Sr/86Sr and 1/Sr, indicating that the isochron is not a mixing line (Fig. 7E).
Rb-Sr systematics of SBS illitic clays
The mixed layer illite/smectite (I/S) is the dominant clay species in all the analyzed samples, totaling more than 50% of the entire clay composition (Table 1). The good negative correlation of 87Rb/86Sr with IR of I/S (Fig. 8A) implies that the 87Rb/86Sr ratio of the samples is controlled by the illitization of I/S. Smectite illitization is a ubiquitous process in the depositional environment41,42. I/S is composed of smectite and illite layers, and the smectite can be transformed to illite with sufficient K supply41,42, as the negative relation between IR values and K contents shows in Fig. 8B. Because Rb has a geochemical behavior similar to K (Fig. 8C), Rb is also introduced to I/S during the illitization process (Fig. 8D). The broad positive correlation between the Sr contents and IR values of I/S indicates that the variation in Sr contents by illitization may be insignificant (Fig. 8E). Therefore, the Rb/Sr fractionation of clay samples is mainly controlled by the addition of Rb during the illitization of I/S. Subsample-scale Rb/Sr fractionation is also observed and the variation in 87Rb/86Sr ratio is generally below 1.5 (Figs 6A–E). Such a small degree of Rb/Sr fractionation may be a response to the microscale chemical variation in the precipitation environment, and each analyzed subsample may contain I/S particles of slightly variable degrees of illitization.
Illitzation has the potential to homogenize the initial Sr isotopic composition of clays and the 87Rb/86Sr and 87Sr/86Sr values for subsamples generally define a linear relation (Figs 6A–E). Regressions of the data of three samples, H6 (Fig. 6B), KQ1 (Fig. 6C) and TZ67 (Fig. 6E), yield isochron ages similar to the corresponding K-Ar ages and reflect the timing of illitization (Table 1). The consistency between Rb-Sr and K-Ar ages suggest that Sr isotopic homogeneity was attained during the illitization. Furthermore, the Rb-Sr age for TZ67 (235 ± 8 Ma, Fig. 6E), which contains 100% I/S (Table 1), has a better precision than H6 (141 ± 61 Ma, Fig. 6B) and KQ1 (332 ± 32 Ma, Fig. 6C), and this suggests that Sr isotopic homogenization may be easier attained within I/S particles than among different Sr-bearing phases (Table 1).
Closed-system behavior is another critical issue for Rb-Sr geochronology6. The isotope chronometer documents the time elapsed since the latest closure of the 87Rb-87Sr isotope system6. The acceptable Rb-Sr ages yielded by samples H6, KQ1 and TZ67 suggest that the Rb-Sr system in these samples did not undergo later disturbance. The Rb-Sr isotope system can show an open-system behavior during the illitization42, since it depends on the temperature and availability of reactants41. Thus, processes that change one of the conditions may terminate illitization and hence maintain a closed-system.
Geological significance of the Rb-Sr isochron ages
Burial-induced temperature increments may increase the degree of illitization of clays, as temperatures increase with depth, facilitating illitization of I/S2,43,44. Burial history analyses show that the maximum temperatures for the Silurian strata in H6, KQ1 and TZ67 were ~138 °C, ~180 °C and ~150 °C, respectively (Figs 9A–C)5,24, and not relevant to the respective IR of I/S (Table 1). Therefore, illitization of I/S in these samples may be more dependent on the availability of reactants.
Potassium, the dominant interlayer cation in illite, is a significant reactant for illitization and is more depleted in hydrocarbons compared to formation water in the reservoir. The hydrocarbon charge may, therefore, inhibit the illitization process and reset the Rb-Sr isotope chronometer3,5. The Rb-Sr ages for H6, KQ1 and TZ67 are consistent with their K-Ar ages and the timing of hydrocarbon charge is constrained by basin modelling (Figs 9A–C. ref.13). Therefore, the Rb-Sr ages likely represent the timing of hydrocarbon charge in respective regions.
The new Rb-Sr age data therefore support the hypothesis of ref.13 that the timing of hydrocarbon charge in the Silurian reservoir varies locally. The hydrocarbon charge occurred earlier in the east of the Manjiaer depression (late Caledonian-Hercynian) compared to the southwest (Indosinian) and northwest of the depression (Yanshanian) (Fig. 9D). The Manjiaer depression is a major tectonic unit accommodating mature source rocks in the Tarim Basin and hydrocarbons discovered in the SBS around the depression have been demonstrated to be generated by source rocks within the depression45. Modelling implies that source rocks in the east side of the Majiaer Depression reached the maturity window earlier than in the west side of the depression45, resulting in the earlier timing of hydrocarbon accumulation in KQ1 than H6 and TZ67 (Fig. 9D). The earlier timing of hydrocarbon charge in TZ67 than in H6 may be due to the shorter distance between drillhole TZ67 and the source kitchen, which was located near the Tazhong uplift during the late Hercynian5.
Implications for Rb-Sr clay hydrocarbon charge geochronology
This study presents new Rb-Sr isotope data for five SBS illitic clay samples from the Tarim Basin and shows that a sufficient spread in 87Rb/86Sr occurs at the subsample scale to allow construction of an isochron. Regressions of Rb-Sr data for samples H6, KQ1, and TZ67 yield three ages: 141 ± 61 Ma (2σ, Fig. 6B), 332 ± 32 Ma (2σ, Fig. 6C) and 235 ± 8 Ma (2σ, Fig. 6E), respectively. These Rb-Sr isochron ages are consistent with the timing of hydrocarbon charge as determined by K-Ar geochronology (125 Ma, 389 Ma and 234 Ma, respectively, Table 1) and basin modelling results13. Therefore, the dating method used in this study has the potential to broadly constrain the timing of hydrocarbon charge.
The Rb-Sr isotope data of samples YM35-1 and Q1 did not yield acceptable isochron ages (Fig. 6A,D). For the mixed-layer illite/smectite, the K and Ar atoms reside in the interlayer space6. The closure of the K-Ar isotope system is mainly influenced by heat-induced Ar-exchange46 and the closure temperature is estimated to be 260 ± 30 °C47. The burial history of the studied area shows that the maximum temperature of Silurian strata was 100–180 °C, which is below this temperature48. Therefore, the K-Ar isotope system is unlikely to be disturbed by later events. For the Rb-Sr isotope system, besides being hosted in the interlayer sites, a portion of the Rb-Sr atoms are absorbed by the external surface of I/S particles49,50. The Rb-Sr atoms hosted by the interlayer sites should be inert to external influence, whereas those absorbed by the external surface are readily removed by hydrothermal fluids46. Therefore, the Rb-Sr isotope system in I/S is more sensitive to hydrothermal fluids46. There was widespread hydrothermal flow in the Tarim Basin during the early Permian, associated with the 300−275 Ma Tarim Large Igneous Province (LIP)51,52. The hydrothermal events extensively influenced the western and Central Tarim Basin (Fig. 1B)53,54,55. Sample KQ1 was collected from the eastern Tarim Basin, where the influence of the Tarim LIP is insignificant (Fig. 1B), whereas samples YM35-1, H6, Q1 and TZ67 were collected from the area affected by the Tarim LIP (Fig. 1B). The hydrocarbon charge in samples H6 and TZ67 occurred subsequent to the Tarim LIP (Fig. 10)13, thus, the Rb-Sr isotope system in these samples can record the timing of hydrocarbon charge, which is the latest event in the region. In contrast, the timing of hydrocarbon charge in samples YM35-1 and Q1 is older than the Tarim LIP (Fig. 10). Therefore, the Rb-Sr isotope chronometer that originally recorded the timing of hydrocarbon charge was most likely disturbed by hydrothermal activity (e.g. hydrothermal leaching of Rb/Sr atoms at easily-exchangeable sites of clays) associated with the LIP. Hydrothermal alteration may result in extensive subsample-scale redistribution of Rb-Sr atoms (e.g. sample YM35-1), or Sr isotopic heterogeneity, which further results in an apparent age for Q1 (484 Ma, an early Ordovician age) that is older than the formation age of the host (early Silurian).
This study involved subsample scale (3–4 mg) Rb-Sr isotopic analysis of illtic clays utilizing samples from the Silurian bituminous sandstone (SBS) in the Tarim Basin, NW China. The results show that the Rb-Sr dating method has potential for dating hydrocarbon systems.
(1) The Rb-Sr analyses for samples H6, KQ1 and TZ67 yield isochron ages of 141 ± 61 Ma, 332 ± 32 Ma and 235 ± 8 Ma (errors quoted at 2σ), respectively. These ages are similar to the corresponding K-Ar ages (125 Ma, 389 Ma and 234 Ma, respectively), previously determined on the same samples in ref.13.
(2) Mixed-layer illite/smectite (I/S) is the dominant clay species (>50%) in all the samples. The illitization of smectite layers in I/S introduces Rb to clays, thus fractionating the 87Rb/86Sr ratios. Minor Rb/Sr fractionation is observed at the subsample scale and suggests that each subsample may contain I/S particles of slightly variable degree of illitization. Smectite illitization also has the potential to homogenize the initial Sr isotopic composition of clays as evidenced by the Rb-Sr isochrons yielded in this study. Hydrocarbon charge may cease the illitization process and result in closed-system behavior of the Rb-Sr isotope system in clays. Therefore, the Rb-Sr isochron ages for samples H6, KQ1 and TZ67 are interpreted as recording the timing of hydrocarbon charge: they are consistent with basin modelling results.
(3) Rb-Sr isotope analysis for samples YM35-1 and Q1 did not yield acceptable isochrons for constraining the timing of hydrocarbon charge. This may be caused by post-charge hydrothermal activity associated with the early Permian Tarim LIP. Hydrothermal alteration may result in extensive subsample-scale redistribution of Rb-Sr atoms (e.g. sample YM35-1), or generate Sr isotopic heterogeneity, which results in an apparent age that is older than the formation age of the host (e.g. Q1).
Busch, B., Hilgers, C., Lander, R. H., Bonnell, L. M. & Adelmann, D. Reservoir quality and burial model evaluation by kinetic quartz and illite cementation modeling: Case study of Rotliegendes, north Germany. AAPG Bulletin 102, 293–307 (2018).
Ehrenberg, S. & Nadeau, P. Formation of diagenetic illite in sandstones of the Garn Formation, Haltenbanken area, Mid-Norwegian continental shelf. Clay Minerals 24, 233–253 (1989).
Hamilton, P., Kelley, S. & Fallick, A. E. K-Ar dating of illite in hydrocarbon reservoirs. Clay Minerals 24, 215–231 (1989).
Pollastro, R. M. Considerations and applications of the illite/smectite geothermometer in hydrocarbon-bearing rocks of Miocene to Mississippian age. Clays and Clay minerals 41, 119–119 (1993).
Zhang, Y., Zwingmann, H., Liu, K., Todd, A. & Luo, X. Hydrocarbon charge history of the Silurian bituminous sandstone reservoirs in the Tazhong uplift, Tarim Basin, China. AAPG bulletin 95, 395–412 (2011).
Clauer, N., Williams, L. B. & Fallick, A. E. Genesis of nanometric illite crystals elucidated by light-element (hydrogen, lithium, boron and oxygen) isotope tracing, and K–Ar and Rb–Sr dating. Chemical Geology 383, 26–50 (2014).
Gorokhov, I., Siedlecka, A., Roberts, D., Melnikov, N. & Turchenko, T. Rb–Sr dating of diagenetic illite in Neoproterozoic shales, Varanger Peninsula, northern Norway. Geological Magazine 138, 541–562 (2001).
Morton, J. P. Rb-Sr dating of diagenesis and source age of clays in Upper Devonian black shales of Texas. Geological Society of America Bulletin 96, 1043–1049 (1985).
Uysal, I. T., Golding, S. D. & Thiede, D. S. K–Ar and Rb–Sr dating of authigenic illite–smectite in Late Permian coal measures, Queensland, Australia: implication for thermal history. Chemical Geology 171, 195–211 (2001).
Zwingmann, H., Clauer, N. & Gaupp, R. Structure-related geochemical (REE) and isotopic (K-Ar, Rb-Sr, δ18O) characteristics of clay minerals from Rotliegend sandstone reservoirs (Permian, northern Germany). Geochimica et Cosmochimica Acta 63, 2805–2823 (1999).
Wasserburg, G., Hayden, R. & Jensen, K. J. A40-K40 dating of igneous rocks and sediments. Geochimica et Cosmochimica Acta 10, 153–165 (1956).
Clauer, N. The K-Ar and 40Ar/39Ar methods revisited for dating fine-grained K-bearing clay minerals. Chemical Geology 354, 163–185 (2013).
Zhang, Y., Liu, K. & Luo, X. Evaluation of 40Ar/39Ar Geochronology of Authigenic Illites in Determining Hydrocarbon Charge Timing: A Case Study from the Silurian Bituminous Sandstone Reservoirs, Tarim Basin, China. Acta Geologica Sinica (English Edition) 90, 684–703 (2016).
Clauer, N., Jourdan, F. & Zwingmann, H. Dating petroleum emplacement by illite 40Ar/39Ar laser stepwise heating: Discussion. AAPG Bulletin 95, 2107–2111 (2011).
Yun, J.-B., Shi, H.-S., Zhu, J.-Z., Zhao, L.-H. & Qiu, H.-N. Dating petroleum emplacement by illite 40Ar/39Ar laser stepwise heating. AAPG bulletin 94, 759–771 (2010).
Middleton, A. W., Uysal, I. T., Bryan, S. E., Hall, C. M. & Golding, S. D. Integrating 40Ar–39Ar, 87Rb–87Sr and 147Sm–143Nd geochronology of authigenic illite to evaluate tectonic reactivation in an intraplate setting, central Australia. Geochimica et Cosmochimica Acta 134, 155–174 (2014).
Bofinger, V., Compston, W. & Vernon, M. The application of acid leaching to the Rb-Sr dating of a Middle Ordovician shale. Geochimica et Cosmochimica Acta 32, 823–833 (1968).
Morton, J. P. Rb-Sr evidence for punctuated illite/smectite diagenesis in the Oligocene Frio Formation, Texas Gulf Coast. Geological Society of America Bulletin 96, 114–122 (1985).
Mutlu, H. et al. Rb–Sr systematics of fault gouges from the North Anatolian Fault Zone (Turkey). Journal of Structural Geology 32, 216–221 (2010).
Clauer, N., Chaudhuri, S., Kralik, M. & Bonnot-Courtois, C. Effects of experimental leaching on Rb|Sr and K| Ar isotopic systems and REE contents of diagenetic illite. Chemical Geology 103, 1–16 (1993).
Li, C.-F. et al. A rapid single column separation scheme for high-precision Sr–Nd–Pb isotopic analysis in geological samples using thermal ionization mass spectrometry. Analytical. Methods 7, 4793–4802 (2015).
Li, C.-F., Guo, J.-H., Chu, Z.-Y., Feng, L.-J. & Wang, X.-C. Direct High-Precision Measurements of the 87Sr/86Sr Isotope Ratio in Natural Water without Chemical Separation Using Thermal Ionization Mass Spectrometry Equipped with 1012 Ω Resistors. Analytical chemistry 87, 7426–7432 (2015).
Zhu, G. et al. Alteration and multi-stage accumulation of oil and gas in the Ordovician of the Tabei Uplift, Tarim Basin, NW China: Implications for genetic origin of the diverse hydrocarbons. Marine and Petroleum Geology 46, 234–250 (2013).
Zhu, G. et al. The occurrence of ultra-deep heavy oils in the Tabei Uplift of the Tarim Basin, NW China. Organic Geochemistry 52, 88–102 (2012).
Zhu, G. et al. A well-preserved 250 million-year-old oil accumulation in the Tarim Basin, western China: Implications for hydrocarbon exploration in old and deep basins. Marine and Petroleum Geology 43, 478–488 (2013).
Zhu, G. et al. Accumulation and reformation of Silurian reservoir in the northern Tarim Basin. Acta geologica sinica (English edition) 86, 209–225 (2012).
Hanson, A., Zhang, S., Moldowan, J., Liang, D. & Zhang, B. Molecular organic geochemistry of the Tarim Basin, northwest China. AAPG bulletin 84, 1109–1128 (2000).
Hu, S., Wilkes, H., Horsfield, B., Chen, H. & Li, S. On the origin, mixing and alteration of crude oils in the Tarim Basin. Organic Geochemistry 97, 17–34 (2016).
Huang, H., Zhang, S. & Su, J. Palaeozoic oil–source correlation in the Tarim Basin, NW China: A review. Organic Geochemistry 94, 32–46 (2016).
Jia, C. & Wei, G. Structural characteristics and petroliferous features of Tarim Basin. Chinese Science Bulletin 47, 1–11 (2002).
Kang, Y. & Kang, Z. Tectonic evolution and oil and gas of Tarim Basin. Journal of Southeast Asian Earth Sciences 13, 317–325 (1996).
Li, S. et al. Origin and quantitative source assessment of deep oils in the Tazhong Uplift, Tarim Basin. Organic Geochemistry 78, 1–22 (2015).
Luo, X., Zhao, Z. & Meng, Y. Application of an odd/even predominance of n-alkanes in oil–source rock correlation: taking the lower Paleozoic strata of the Tarim Basin as an example. Toxicological & Environmental Chemistry 97, 409–416 (2015).
Xiao, Z. et al. Source, oil charging history and filling pathways of the Ordovician carbonate reservoir in the Halahatang Oilfield, Tarim Basin, NW China. Marine and Petroleum Geology 73, 59–71 (2016).
Guo, X. et al. Hydrocarbon accumulation processes in the Dabei tight-gas reservoirs, Kuqa Subbasin, Tarim Basin, northwest China. AAPG Bulletin 100, 1501–1521 (2016).
Tian, H. et al. Formation and evolution of Silurian paleo-oil pools in the Tarim Basin, NW China. Organic Geochemistry 39, 1281–1293 (2008).
Clauer, N., Giblin, P. & Lucas, J. Sr and Ar isotope studies of detrital smectites from the Atlantic Ocean (DSDP, Legs 43, 48 and 50). Chemical geology 46, 141–151 (1984).
Clauer, N., Środoń, J., Francu, J. & Šucha, V. K-Ar dating of illite fundamental particles separated from illite-smectite. Clay Minerals 32, 181–196 (1997).
Ludwig, K. User’s manual for Isoplot 3.00: a geochronological toolkit for Microsoft Excel. Barkeley Geochronology Center. Special publication 4, 1–71 (2003).
Rotenberg, E., Davis, D. W., Amelin, Y., Ghosh, S. & Bergquist, B. A. Determination of the decay-constant of 87Rb by laboratory accumulation of 87Sr. Geochimica et Cosmochimica Acta 85, 41–57 (2012).
Bethke, C. M., Vergo, N. & Altaner, S. P. Pathways of smectite illitization. Clays and Clay Minerals. 34, 125–135 (1986).
Altaner, S. P. & Ylagan, R. F. Comparison of structural models of mixed-layer illite/smectite and reaction mechanisms of smectite illitization. Clays and Clay Minerals 45, 517–533 (1997).
Franks, S. G. & Zwingmann, H. Origin and timing of late diagenetic illite in the Permian–Carboniferous Unayzah sandstone reservoirs of Saudi Arabia. AAPG Bulletin 94, 1133–1159 (2010).
Środo, J., Clauer, N., Huff, W., Dudek, T. & Bana, M. K-Ar dating of the Lower Palaeozoic K-bentonites from the Baltic Basin and the Baltic Shield: implications for the role of temperature and time in the illitization of smectite. Clay Minerals 44, 361–387 (2009).
Zhao, M.-J. et al. Lower palaeozoic source rocks in Manjiaer sag, Tarim Basin. Petroleum Exploration and Development 35, 417–423 (2008).
Kralik, M. Interpretation of K–Ar and Rb–Sr data from fine fractions of weakly metamorphosed shales and carbonate rocks at the base of the northern calcareous Alps (Salzburg, Austria). Tschermaks Mineralogische und Petrographische Mitteilungen 32, 49–67 (1983).
Evans, J. Dating the transition of smectite to illite in Palaeozoic mudrocks using the Rb–Sr whole-rock technique. Journal of the Geological Society 153, 101–108 (1996).
Youyu, Z., Keyu, L. & Xiuquan, L. Geochronology of Authigenic Illite: Principles, Methods and Applications. Science Press. Beijing. 184, 313 (2016).
Chaudhuri, S. & Brookins, D. G. The Rb-Sr systematics in acid-leached clay minerals. Chemical Geology 24, 231–242 (1979).
Gorokhov, I. et al. Rb-Sr systematics of Vendian-Cambrian claystones from the east European Platform: implications for a multi-stage illite evolution. Chemical Geology 112, 71–89 (1994).
Xu, Y.-G., Wei, X., Luo, Z.-Y., Liu, H.-Q. & Cao, J. The Early Permian Tarim Large Igneous Province: main characteristics and a plume incubation model. Lithos 204, 20–35 (2014).
Zhou, M.-F. et al. OIB-like, heterogeneous mantle sources of Permian basaltic magmatism in the western Tarim Basin, NW China: implications for a possible Permian large igneous province. Lithos 113, 583–594 (2009).
Cai, C., Li, K., Li, H. & Zhang, B. Evidence for cross formational hot brine flow from integrated 87Sr/86Sr, REE and fluid inclusions of the Ordovician veins in Central Tarim, China. Applied Geochemistry 23, 2226–2235 (2008).
Li, K. et al. Origin of palaeo‐waters in the Ordovician carbonates in Tahe oilfield, Tarim Basin: constraints from fluid inclusions and Sr, C and O isotopes. Geofluids 11, 71–86 (2011).
Jin, Z., Zhu, D., Zhang, X., Hu, W. & Song, Y. Hydrothermally fluoritized Ordovician carbonates as reservoir rocks in the Tazhong area, central Tarim Basin, NW China. Journal of Petroleum Geology 29, 27–40 (2006).
This work was supported by the Science Foundation of Chang’an University (grant number 310827163412), and Strategic Priority Research Program of the Chinese Academy of Sciences (Grant No. XDA14010401). We would like to express special thanks to editor Dan Zhu for handling the manuscript and two anonymous reviewers for their constructive comments.
The authors declare no competing interests.
Publisher’s note: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
About this article
Cite this article
Li, S., Wang, X., Li, C. et al. Direct Rubidium-Strontium Dating of Hydrocarbon Charge Using Small Authigenic Illitic Clay Aliquots from the Silurian Bituminous Sandstone in the Tarim Basin, NW China. Sci Rep 9, 12565 (2019) doi:10.1038/s41598-019-48988-3