Abstract
Light oil is a high-quality crude oil. The formation and chemical composition of light oil is a matter of great concern to petroleum geologists. Yakela Field and Shunbei Field, which are located in Yakela and Shunbei regions, respectively, are the two main light oil fields in the Tabei uplift of the Tarim Basin. In order to identify the causative mechanism of light oils in these two fields, 17 crude oil samples were selected and analyzed by gas chromatography (GC) for saturated hydrocarbons and gas chromatography–mass spectrometry (GCMS) for saturated and aromatic biomarkers. Then, the compounds were measured via the mass spectrometry detector after GC separation. The molecular geochemical characteristics showed that the light oils in the two fields are sourced from similar marine source rocks deposited under weak oxidative and reductive environments. The maturity of crude oil in the Shunbei Field is higher than that in the Yakela Field. Simulation results of hydrocarbon generation history of source rocks in two fields showed that the formation mechanism of the two light oils is different. The light oil in the Yakela Field is directly generated by the source rock in the late oil-generating window. The crude oil in the Shunbei Field is formed by the deep burial and maturation of the crude oil generated in the early stage of the source rock.
1 Introduction
Light oil refers to crude oil with an API higher than 36° (). Compared to normal crude oil, light oil has a higher economic value (). Therefore, the formation and composition of light oil is a matter of great concern to petroleum geologists. Previous research suggests that light oils have multiple mechanisms of formation. The formation of light oil is mainly related to the type of parent material, the degree of thermal evolution, and the secondary alteration processes within the reservoir. Humic-type organic matter can produce a small amount of light oil (; ; ). Sapropel-type organic matter can generate a certain amount of light oil in the high evolution stage. High-temperature thermal cracking can break the carbon chain of normal oil to form light oil. Gas invasion can separate short-chain hydrocarbons from normal crude oil to form light oil. Light oils formed by different formation mechanisms are often different (). In general, light oils formed by high-temperature thermal cracking of crude oil are often larger than those formed by other mechanisms (). Therefore, the identification of the genetic type of light oil is of great significance for the exploration (; ).
The Tarim Basin is the largest petroleum-bearing basin in China. The Tabei uplift is the most abundant oil and gas zone in the Tarim Basin (; ). There are various types of crude oil in the Tabei uplift, including heavy oil, normal oil, and light oil. Heavy oil accounts for the vast majority of crude oil in the uplift and is thought to be due to biodegradation (; ). Light oil mainly exists in the southern Shunbei region and the northern Yakela region. Although previous studies have been carried out on the origin of light oil in the Tarim Basin, most of them are related to secondary alteration processes, such as gas washing and fractionation (). The genetic mechanism of light oil in the Shunbei and Yakela fields has not been systematically studied. In this study, the geochemical characteristics of light oil in these two fields will be systematically investigated in order to identify its causative mechanism. The study is of great significance for clarifying the genetic mechanism and identifying the source of light oils in the Tarim Basin and the discovery of new large-scale oil and gas fields.
2 Geological setting
The Tarim Basin, with an area of approximately 5.6×105 km2, is the largest petroliferous basin in China (Figure 1A). It is a typical superimposed basin in western China, consisting of Paleozoic cratons in the lower part and Mesozoic–Cenozoic foreland depressions in the upper part (; ; ). The basin is bounded by the Tianshan Mountains in the north, the Kunlun Mountains in the southwest, and the Altyn Mountains in the southeast. The first-level tectonic units in the basin include the Tabei uplift, Tazhong uplift, Kuqa depression, Northern depression, Southwest depression, and Southeast fault-uplift belt (Figure 1A) (; ). The Tarim Basin has a complex history of tectonic movements, which has experienced three major tectonic events in the late Caledonian, late Hercynian, and Yanshan–Himalayan periods (; ). The sedimentary strata of Tarim Basin include the Sinian–Devonian marine sedimentary strata, the Carboniferous–Permian marine-continental transitional strata, and the Triassic–Quaternary terrestrial sedimentary strata (Figure 2) (; ). Organic-rich shale of the Lower Cambrian Yuertusi Formation (Є1y) was widely developed in the Tabei uplift, which is the main source rock of the uplift (; ). The source rock was mainly composed of two types of organic facies, namely, planktonic algae in undercompensated basin and planktonic algae in evaporative lagoon. The source rock was widely distributed, with high organic matter abundance and maturity. The organic facies of source rocks in Shunbei Field and Yakela Field were mainly planktonic algae in undercompensated basin (; ). The middle Ordovician Yijianfang Formation (O2yj) and the upper Yingshan Formation (O1-2y) are the main reservoirs in Shunbei Field (; ). The Lianglitage (O3l) and Sangtamu (O3s) Formations provide excellent regional cap rocks for the preservation of deep oil and gas accumulations (Figure 2) (). The lower Cretaceous Yageliemu Formation (K1y) is the main reservoir, and the Xiaokuzibai Formation (E2k) provide the cap rocks in Yakela Field (; ).
FIGURE 1
FIGURE 2
After decades of oil and gas exploration and development, several large deep oil and gas fields such as Tahe, Halahatang, and Tazhong oil fields have been discovered in Tabei uplift, Tazhong uplift, and other areas, with total oil and gas reserves of more than 1×1010 tons (7.3×1010 barrels) (
Shunbei Field is located in the south of Tabei uplift and at the center of Tarim Basin. It is located between Awati Depression and Manjiaer Depression and is located in the “saddle” of relatively low structure (
3 Samples and methods
3.1 Sample selection and pretreatment
A total of 17 representative crude oil samples were selected for this study: 6 from Yakela Field and 11 from Shunbei Field in the Tabei area. (Figure 1B and Table 1). Samples of crude oil were sealed and refrigerated in dark brown glass bottles to prevent the loss of light components due to light and temperature increases. Crude oil samples of about 20 mg were dissolved by adding n-hexane, thoroughly shaken, and kept for 12 h. Asphaltene was obtained by filtering using cotton. Saturated hydrocarbon, aromatic hydrocarbon, and polar hydrocarbon fractions were obtained by filtration of alumina and silica gel using n-hexane, dichloromethane/n-hexane (2:1, v/v), and dichloromethane/methanol (93:7, v/v) as solvents, respectively.
TABLE 1
| Well | Depth (m) | Fm | A1 | A2 | A3 | A4 | A5 | A6 | A7 | A8 |
|---|---|---|---|---|---|---|---|---|---|---|
| Y1 | 5,278 | K1y | 0.39 | 0.68 | 1.01 | 0.33 | 0.29 | 0.28 | 0.24 | 0.48 |
| Y2 | 5,202 | K1y | 0.41 | 0.70 | 1.16 | 0.38 | 0.35 | 0.33 | 0.29 | 0.38 |
| Y3 | 5,275 | K1y | 0.35 | 0.64 | 1.24 | 0.30 | 0.28 | 0.33 | 0.22 | 0.45 |
| Y4 | 5,240 | K1y | 0.39 | 0.71 | 1.02 | 0.54 | 0.47 | 0.35 | 0.20 | 0.45 |
| Y5 | 5,228 | K1y | 0.40 | 0.70 | 1.06 | 0.49 | 0.45 | 0.36 | 0.18 | 0.46 |
| Y6 | 5,267 | K1y | 0.39 | 0.68 | 1.00 | 0.52 | 0.44 | 0.34 | 0.23 | 0.42 |
| S1 | 7,458 | O1-2y | 0.65 | 0.50 | 0.98 | 0.52 | 0.46 | 0.32 | 0.24 | 0.44 |
| S2 | 7,469 | O1-2y | 0.52 | 0.53 | 0.97 | 0.52 | 0.47 | 0.41 | 0.20 | 0.39 |
| S3 | 7,455 | O1-2y | 0.58 | 0.51 | 0.96 | 0.52 | 0.46 | 0.37 | 0.23 | 0.40 |
| S4 | 7,459 | O1-2y | 0.62 | 0.53 | 0.94 | 0.53 | 0.46 | 0.38 | 0.20 | 0.42 |
| S5 | 7,474 | O1-2y | 0.46 | 0.52 | 0.97 | 0.52 | 0.46 | 0.38 | 0.20 | 0.42 |
| S6 | 7,488 | O1-2y | 0.50 | 0.53 | 0.96 | 0.53 | 0.46 | 0.34 | 0.22 | 0.44 |
| S7 | 7,399 | O1-2y | 0.44 | 0.52 | 0.94 | 0.54 | 0.47 | 0.37 | 0.18 | 0.45 |
| S8 | 7,448 | O1-2y | 0.46 | 0.57 | 0.97 | 0.49 | 0.45 | 0.38 | 0.23 | 0.39 |
| S9 | 7,415 | O1-2y | 0.72 | 0.51 | 0.96 | 0.52 | 0.46 | 0.34 | 0.24 | 0.42 |
| S10 | 7,460 | O1-2y | 0.41 | 0.67 | 0.95 | 0.54 | 0.47 | 0.38 | 0.21 | 0.42 |
| S11 | 7,465 | O1-2y | 0.41 | 0.65 | 0.96 | 0.55 | 0.49 | 0.34 | 0.25 | 0.41 |
Organic molecular parameters of oil samples from Yakela Field and Shunbei Field.
Y: Yakela; S: Shunbei; Fm.: formation; K1y: Yageliemu Formation; O1-2y: Yingshan Formation; A1=C22TT/C21TT; A2= C24TT/C23TT; A3=Pr/Ph; A4= Ph/nC18; A5= Pr/nC17; A6= C27/(C27+C28+C29)ααα20R sterane; A7= C28/(C27+C28+C29)ααα20R sterane; A8= C29/(C27+C28+C29)ααα20R sterane.
3.2 Gas chromatography and gas chromatography–mass spectrometry analysis
Saturated hydrocarbons from the reservoir oils and reservoir extracts were firstly analyzed via gas chromatography (GC) using an Agilent 7890 A gas chromatograph fitted with a 25 m × 0.20 mm i. d. DB-5 column with a film thickness of 0.33 μm and using helium as carrier gas at a constant flow mode. The GC oven temperature was initially set to 60°C for 1 min, ramped from 60 to 310°C at 7°C/min, and then held at 310°C for 20 min. Separated n-alkane and isoprenoid compounds were then analyzed using the Agilent 5977B MSD mass spectrometry detector. Gas chromatography–mass spectrometry analysis of saturated and aromatic hydrocarbon biomarkers was performed on an Agilent gas chromatography–mass spectrometry 8,860 GC-5977B MSD gas chromatography mass spectrometer. The chromatographic column model was HP-5 quartz elastic capillary (60 m×0.32 mm×0.25 μm). Samples were injected in a pulsed splitless mode, the temperature of the injector was 300°C, the carrier gas was helium, the flow rate was 1 ml/min, the ionization energy was 70 eV, and the detection method was full scan (SCAN)/selected ion monitoring (SIM). The saturated hydrocarbon heating program condition was as follows: initial temperature of 50°C, maintained for 1 min, increased to 120°C at 20°C/min, increased to 310°C at 3°C/min, and maintained for 25 min. The heating program of aromatic hydrocarbon was as follows: the initial temperature was 80°C, increased to 310°C at 3°C/min, and held for 25 min. The separation of crude oil components, gas chromatography, and gas chromatography–mass spectrometry experiments were performed in the experimental research center of Wuxi research institute of petroleum geology of SINOPEC.
3.3 Basin numerical simulation
In this study, the numerical simulation of geological history and hydrocarbon generation history was mainly carried out using Petromod software. Prior to the simulation, parameters such as depth, lithology, deposition and denudation age, denudation thickness, sedimentary palaeowater depth, geochemical indexes of source rocks, and hydrocarbon-generation dynamics model were input. The TⅡ kerogen kinetic model by
4 Results and discussion
4.1 Geochemical characteristics of light oils
4.1.1 Sedimentary environment and source of parent material for crude oil
As for isoprenoids, the pristane/phytane (Pr/Ph) ratios of crude oils in Yakela Field range from 1.00 to 1.24, with an average of 1.08. The Ph/nC18 ratio ranges from 0.30 to 0.54, with an average value of 0.43. The Pr/nC17 ratio ranges from 0.28 to 0.47, with an average value of 0.38. However, the Pr/Ph value of crude oils in Shunbei Field is 0.94–0.98, with an average of 0.96. The Ph/nC18 ratio was 0.49–0.55, with an average value of 0.53. The ratio of Pr/nC17 was 0.45–0.49, with an average of 0.46 (Table 1). The Pr/Ph of crude oils in Shunbei Field is lower than those in Yakela Field, but the Ph/nC18 and Pr/nC17 ratios are higher on the whole.
The most abundant sources of Pr and Ph are chlorophyll A in photosynthetic organisms and the phytological side chains of bacterial chlorophyll A and B in purple sulfur bacteria (
FIGURE 3

Cross plots of biomarker ratios: (A) Pr/nC17 vs. Ph/nC18; (B) C24TT/C23TT vs. C22TT/C21TT; (C) Triangular plot of the normalized relative abundances of C27–C29 ααα 20R steranes (modified from Connan and Cassau, 1980;
Representative m/z191 chromatograms of the saturated fraction are shown in Figure 4. Terpanes such as tricyclic terpanes (TT), pentacyclic terpanes, and C24 tetracyclic terpanes can be detected in crude oil samples from both regions. The C22TT/C21TT ratios of crude oils in Yakela Field range from 0.35 to 0.41, with an average of 0.39. The C24TT/C23TT ratio range from 0.64 to 0.71, with an average value of 0.68. However, the C22TT/C21TT value of crude oils in Shunbei Field is 0.41–0.72, with an average of 0.52. The C24TT/C23TT ratio is 0.50–0.67, with an average value of 0.55 (Table 1).
FIGURE 4

Representative gas chromatography (GC) and m/z191 and m/z217 mass chromatograms of the saturated hydrocarbon fraction for oils samples. (A)Y1, K1b; (B) S1, O1-2y.
The ratios of C22TT/C21TT and C24TT/C23TT can be used to identify the type of source rock for crude oils (
Representative m/z217 chromatograms of the saturated fraction are shown in Figure 4. Steranes, such as regular steranes, can be detected in crude oil samples from both regions. The relative abundance of C27, C28, and C2C9 regular steranes is often used to trace source rocks (
4.1.2 Maturity of crude oil in Shunbei and Yakela fields
The ratio of 17α(H)-22,29,30 trisnorhopane (Tm) and 18α(H)-22,29,30 trisnorhopane (Ts) is a commonly used biomarker parameter to reflect the maturity of crude oil (
TABLE 2
| Well | Depth (m) | Fm | B1 | B2 | B3 | B4 | B5 | B6 | B7 | B8 |
|---|---|---|---|---|---|---|---|---|---|---|
| Y1 | 5,278 | K1y | 1.16 | 0.97 | 0.55 | 0.56 | 10.72 | 0.47 | 0.28 | 0.95 |
| Y2 | 5,202 | K1y | 1.14 | 0.98 | 0.55 | 0.63 | 14.00 | 0.50 | 0.33 | 1.06 |
| Y3 | 5,275 | K1y | 1.15 | 0.99 | 0.56 | 0.62 | 12.45 | 0.52 | 0.33 | 1.01 |
| Y4 | 5,240 | K1y | 1.3 | 0.98 | 0.57 | 0.61 | 8.64 | 0.66 | 0.31 | 0.87 |
| Y5 | 5,228 | K1y | 1.15 | 0.99 | 0.58 | 0.58 | 14.00 | 0.63 | 0.36 | 1.06 |
| Y6 | 5,267 | K1y | 1.19 | 0.99 | 0.56 | 0.59 | 9.07 | 0.37 | 0.25 | 0.89 |
| S1 | 7,458 | O1-2y | 1.22 | 0.98 | 0.58 | 0.60 | 25.98 | 0.74 | 0.51 | 1.50 |
| S2 | 7,469 | O1-2y | 1.19 | 1.00 | 0.56 | 0.57 | 19.57 | 0.57 | 0.31 | 1.26 |
| S3 | 7,455 | O1-2y | 1.23 | 0.99 | 0.60 | 0.57 | 26.43 | 0.72 | 0.68 | 1.51 |
| S4 | 7,459 | O1-2y | 1.18 | 1.01 | 0.60 | 0.58 | 26.62 | 0.56 | 0.40 | 1.52 |
| S5 | 7,474 | O1-2y | 1.29 | 0.98 | 0.52 | 0.54 | 26.94 | 0.51 | 0.35 | 1.53 |
| S6 | 7,488 | O1-2y | 1.11 | 0.98 | 0.55 | 0.56 | 25.74 | 0.57 | 0.38 | 1.49 |
| S7 | 7,399 | O1-2y | 1.16 | 0.97 | 0.60 | 0.60 | 26.90 | 0.62 | 0.35 | 1.53 |
| S8 | 7,448 | O1-2y | 1.20 | 0.97 | 0.57 | 0.58 | 21.28 | 0.71 | 0.55 | 1.33 |
| S9 | 7,415 | O1-2y | 1.18 | 0.98 | 0.57 | 0.57 | 21.72 | 0.71 | 0.49 | 1.34 |
| S10 | 7,460 | O1-2y | 1.19 | 0.98 | 0.59 | 0.60 | 18.96 | 0.88 | 0.88 | 1.24 |
| S11 | 7,465 | O1-2y | 1.22 | 0.97 | 0.56 | 0.60 | 26.51 | 0.77 | 0.43 | 1.51 |
Maturity parameters of oil samples from Yakela Field and Shunbei Field.
Y: Yakela; S: Shunbei; Fm.: formation; K1y: Yageliemu Formation; O1-2y: Yijianfang Formation; B1=CPI: 2(C23+C25+C27+C29)/(C22+2(C24+C26+C28) +C30); B2= OEP (C21+6C23+C25)/(4C22+4C24); B3= C29ααα 20S/(20S+20R) sterane; B4= C29αββ/(ααα+αββ) sterane; B5= MDR (4-/1-MDBT); B6= Ts/(Ts+Tm); B7= C29Ts/(C29Ts+C29H); B8=Rc(0.036×(4-/1-MDBT)+0.56).
FIGURE 5

Cross plot showing the maturity of the oils in Yakela Field and Shunbei Field, Tarim Basin. (A) Cross plot of C29Ts/(C29Ts+C29H) and Ts/(Ts+Tm); (B) Cross plot of C29ααα 20S/(20S+20R) sterane and C29αββ/(ααα+αββ) sterane.
N-alkanes in all crude oil samples in the study area are completely distributed, without obvious unresolved complex mixture (UCM) hump. Low carbon number n-alkanes (C6-C12) were not eliminated (Figure 4). At the same time, no 25-norhopane could be identified in all crude oil samples; it indicated that the crude oils from Shunbei Field and Yakela Field have not been subjected to biodegradation (
The isomerization of C295α,14α,17α(H)-steranes on C-20 increases the 20S/(20S+20R) ratio from 0 to an equilibrium value of about 0.5 (0.52–0.55, 0.9%Ro) with increasing maturity (
Alkylated dibenzothiophenes (DBTs), as heterocyclic compounds, are generally assigned to aromatic sulfur compounds. It mainly contains DBT and its C1-∼ C3-substituted alkyl derivatives, which usually exist in the aromatic fractions of crude oil or sediment (Hughes, 1984;
In this study, the values of 4-/1-MDBT of crude oil samples from the Shunbei Field are greater than those from the Yakela Field (Table 2). The equivalent vitrinite reflectance Rc (Rc=0.036×(4-/1-MDBT)+0.56) (
FIGURE 6

Comparison of Rc for the oils in the Yakela Field and Shunbei Field.
To sum up, the crude oils from both Yakela Field and Shunbei Field were in the mature stage, but the parameters reflected the difference in maturity between them to varying degrees. The maturity of crude oils in Yakela Field is in the peak stage of hydrocarbon generation (About 0.9%Ro-1.0%Ro), while that in Shunbei Field has passed the peak stage of hydrocarbon generation (About 1.0%Ro-1.3%Ro, may be up to 1.53%Ro). The maturity of crude oils in Shunbei Field was higher than that in Yakela Field.
4.2 Formation mechanism of light oils
In this study, an approximately NE-SW profile was selected, passing Y1, A1, T1, and S1 Wells from north to south, covering Yakela Field and Shunbei Field (Figure 1). The actual downhole data show that the Lower Cambrian source rocks in Shunbei Field have a high degree of thermal evolution with %Ro over 2.5 at present (Figure 7). However, the thermal evolution degree of the source rocks near Yakela Field in the northern part of the profile is relatively low, with %Ro about 1.50–1.70 (Figure 7).
FIGURE 7

The tectonic profile of the study area contains the current thermal evolution of the source rocks of the Lower Cambrian Yuertusi Formation.
The hydrocarbon generation history of Lower Cambrian Yuertusi Formation source rocks widely distributed in the study area was simulated. The thermal evolution history of source rocks and the simulation results of hydrocarbon generation amount are shown in Figure 8. The hydrocarbon generation history results show that the source rocks in Shunbei Field reached the hydrocarbon generation threshold as early as before the late Caledonian (About 0.5%Ro) and reached the peak of hydrocarbon generation at the late Caledonian (About 1.0%Ro). The source rocks were in the main stage of oil generation from the late Caledonian to the early Hercynian, and from the late Hercynian to the Himalayan period were in the high maturity and over-maturity stage (Figure 8A). The simulation results of hydrocarbon generation amount of source rocks showed that the source rocks mainly generated hydrocarbon from before the late Caledonian to the early Hercynian (About 2.5 Mtons), and the amount of hydrocarbon generated from the late Hercynian to the present is small (About 0.3 Mtons) (Figure 8C). The source rocks near Yakela Field reached the threshold of hydrocarbon generation from late Caledonian to the early Hercynian (About 0.5%Ro) and reached the peak of hydrocarbon generation at the Himalayan period (About 1.0%Ro) (Figure 8B). The simulation results of hydrocarbon generation amount of source rocks showed that the source rocks mainly generated hydrocarbon at the late Hercynian (About 1.0 Mtons) and from the Himalayan period to the present (About 2.5 Mtons). (Figure 8D). These results indicated that the main hydrocarbon generation period of the source rocks in Shunbei Field is different from that of Yakela Field. The former mainly generated hydrocarbons from late Caledonian to early Hercynian, while the latter mainly generated hydrocarbons from the late Hercynian and Himalayan period to the present.
FIGURE 8

Thermal evolution history of source rocks and the amount of hydrocarbon generation in each period. (A) the history of source rocks in Shunbei Field; (B) the history of source rocks in Yakela Field; (C) the amount of hydrocarbon generation in Shunbei Field; (D) the amount of hydrocarbon generation in Yakela Field.
Therefore, the maturity of crude oils in Yakela Field is consistent with the degree of the thermal evolution of source rocks since the Himalayan period (Figures 8B and 5). However, the maturity of crude oils in Shunbei Field is higher than the degree of the thermal evolution of local source rocks during the peak of hydrocarbon generation (Figures 8A and 5). It indicates that the high-maturity crude oils in the two areas have different genetic models.
The genetic model of light oils in Shunbei Field is mainly through early oil generation, early charging, and then deep burial in the reservoir, with subsequent maturation cracking. The maturity of crude oils in the present reservoir (About 1.0%Ro-1.3%Ro, may be up to 1.53%Ro) is higher than the thermal evolution of source rocks in the main hydrocarbon generation stage (About 0.8%Ro-1.0%Ro). When the source rock evolved to the maturity corresponding to the present crude oils, it was already in the mature and high mature stage, and the amount of hydrocarbon generation was very small (About 0.3 Mtons). Therefore, the existing high-maturity crude oils cannot be directly generated by source rocks and should be the result of deep burial and maturation in the reservoirs.
The genetic model of light oils in the Yakela Field is mainly formed by the direct charging of late source rocks into reservoirs. The simulation results of hydrocarbon generation history show that the source rocks are in the window of hydrocarbon generation, and the amount of hydrocarbon generation has been high (About 2.5 Mtons) since the Himalayan period. The maturity of crude oils in the present reservoirs (About 0.9%Ro-1.0%Ro) is also consistent with the thermal evolution stage of source rocks in the main hydrocarbon generation stage. It also indicates that hydrocarbons generated from source rocks in this field were directly charged into the reservoirs during hydrocarbon generation and maintained the thermal evolution characteristics of the source rocks without the interference of subsequent geologic alteration processes such as deep burial and maturation such as the secondary thermal cracking.
5 Conclusion
1) The molecular geochemical characteristics show that the light oils in the two areas are sourced from similar marine source rocks deposited under the weak oxidative and reductive environment. The maturities of crude oils in Yakela Field and Shunbei Field were in the mature stage, but the parameters reflected the difference in maturity between them to varying degrees. On the whole, the maturity of crude oil in Shunbei Field was higher than that in Yakela Field.
2) The formation mechanism of the two light oils is different. The light oil in Yakela Field was directly generated by the source rock in the oil-generating window. The crude oil in Shunbei Field was formed by the deep burial and maturation of the crude oil generated in the early stage of the source rock. This study is of great significance for further clarifying the genesis mechanism of light oil and gas in the deep Tarim Basin, guiding further deep oil and gas exploration and discovering new large-scale condensate and natural gas fields.
Statements
Data availability statement
The original contributions presented in the study are included in the article/Supplementary Material; further inquiries can be directed to the corresponding author.
Author contributions
All authors listed have made a substantial, direct, and intellectual contribution to the work and approved it for publication.
Funding
This study was funded by the Strategic Priority Research Program of the Chinese Academy of Sciences (Grant No. XDA14010305) and the National Natural Science Foundation of China (Grants Nos. 41821002 and 41872159).
Conflict of interest
YW was employed by Northwest Oil Company, SINOPEC.
The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Publisher’s note
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Summary
Keywords
light oil, genesis, Shunbei, Yakela, maturation
Citation
Wang Y, Zhang S, Xie H, Wang Q and Tian J (2023) Characteristics and genesis of light oil in Tabei Area, Tarim Basin, Northwestern China. Front. Earth Sci. 10:922311. doi: 10.3389/feart.2022.922311
Received
17 April 2022
Accepted
01 August 2022
Published
11 January 2023
Volume
10 - 2022
Edited by
Tao Wen, Syracuse University, United States
Reviewed by
Palma Botterell, United States Geological Survey (USGS), United States
Yan Li, Jinan University, China
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© 2023 Wang, Zhang, Xie, Wang and Tian.
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*Correspondence: Jinqiang Tian, tianjq@upc.edu.cn
This article was submitted to Geochemistry, a section of the journal Frontiers in Earth Science
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