Cutting samples (n = 93) from the Sirte, Tagrifet, Rakb, Rachmat, Bahi Formations of Upper Cretaceous and Nubian Formation (Lower Cretaceous) derived from eleven wells (6C1-59, 6J1-59, 6R1-59, KK1-65, OO2-65, M1-51, KK1-65, B-96, B-95, B-99, E1-NC-59) locate in the Amal, Gialo, Nafoora, and Sarir Fields present in East Sirte Basin were analysed in the aim of their organic geochemical evaluation. A bulk geochemical parameters and evaluation of specific biomarkers by chromatography-mass spectrometry (GC-MS) implemented to find out a diversity of interbedded non-marine lithofacies including sandstones, siltstones, shales and conglomerates. Such rocks are good source and contain fair to good contented of organic matter passing in the course of very good, in which the excellent source rocks have organic carbon richness (TOC) reached to 5.16 wt%. The studied samples are ranged from gas to oil-prone organic matter (OM) of hydrogen index (HI) ranged between 115 - 702 mg HC/g TOC, related with gas prone (OM) of (HI) <150 and most beds contain oil-prone organic matter of (HI) > 300, associated with oxygen index (OI): 3 - 309 mg CO2/g TOC indicate that organic matter is dominated by Type II/III kerogen. The maturity of these source rocks is variations ranges from mature to post-mature-oil window in the Sirte and Rachmat Formations, as inferred from the production index (PI: 0.07 - 1.55) and Tmax and Ro% data (Tmax: 425 - 440/Ro%: 0.46 - 1.38) and early to mid-stage maturities for the other formations. Low PI in some samples seems to imply that the most of the hydrocarbons have expelled and migrated from the rocks. Biomarker ratios of individual hydrocarbons in rock extracts (n = 21), were also used in order to investigate the samples’ thermal maturity and palaeo depositional conditions. Pristine/Phytane ratios of 0.65 - 1.25 and dibenzothiophene to phenanthrene (DBT/P) ratios of 0.04 - 0.47 indicated Anoxic and suboxic conditions of depositional source rock. The origin of OM of the studied samples attributed to a marine algal source as indicated from the dominated by the C27 and co-dominant C28 homologues sterane in molecular composition distributions. The marine shale and carbonate lithofacies of rock samples were also indicated by high C19TT/C23TT ratio and low relative abundance of C24TeT/C23TT, consistent with their interpreted marine affinity. An organic geochemical evaluation pointed out that the Sirte Shale formation (Campanian/Turonian) is the main source rock in this petroleum area. 

Tricyclic terpanes to hopanes Ratios calculated from individual biomarkers to delineate their distribution, identifications, mixing ratios and biological precursor in a suite of crude oils (n = 24) from the East Sirt Basin. Geochemical application of Tricyclic terpane and Hopane biomarkers is divided studied oils into five groups (I, II, III, IV and V) based on the different ratios between Tricyclic terpanes to hopanes. Percentages of C23 Tricyclic terpanes/17α (H), 21β(H)-hopanes (C30αβ) and C28 Tricyclic terpane/17α (H), 21β (H)-30 hopanes (C31) have divided crude oils into 2 main individual groups in addition to 3 mixed groups. Group I, characterized by the dominance and extension of the tricycle terpane series (≈ C45 Tricyclic terpane). Group V, distinguished with the dominance of 17α (H), 21β (H) hopanes series. Groups II, contained a domination Tricyclic terpanes and hopanes, considered as a mixed group. The group III demonstrated equivalent ratios of Tricyclic terpanes to hopanes. The Group IV revealed a reduced amount of Tricyclic terpanes with enrich of hopanes. Tricyclic terpanes derived from tricyclohexaprenol precursors and attributed to a marine depositional environment and algal matter. Hopanes in obtained from bacteriohopane polyols and aminopolyols and distinguished to a depositional bacterial environment.

The present paper involves a detailed evaluation of specific steroid biomarkers by gas chromatography– mass spectrometry (GC–MS) and GC-metastable reaction monitoring (MRM) analyses of several crude oils and source rocks from the East Sirte Basin. 24-Norcholestanes, dinosteranes, 4a-methyl-24-ethylcholestanes and triaromatic steroids have been identified in both source-rocks and crude oils of the East Sirte Basin. Diatoms, dinoflagellates (including those potentially associated with corals) and/or their direct ancestors are amongst the proposed sources of these biomarkers. These biomarker parameters have been used to establish a Mesozoic oil–source correlation of the East Sirte Basin. Hydropyrolysis of an extant coral extract revealed a similar distribution (although immature) of dinosteranes and 4a-methyl-24-ethylcholestanes also observed in the Sirte oils and source-rocks. This is consistent with the presence of dinoflagellates present during the deposition of the Mesozoic aged East Sirte Basin Formations. A good data correlation for the rock extracts revealed a similar distribution of 3,24-dimethyl triaromatic steroids, 3-methyl-24-ethylcholestanes, 4-methyl-24-ethylcholestanes and 2-methyl-24-ethylcholestanes observed in one of the oil families and associated source-rocks for the East Sirte Basin.

Biomarker ratios, together with stable carbon (d13C) and hydrogen (dD) isotopic compositions of individual hydrocarbons have been determined in a suite of crude oils (n = 24) from the East Sirte Basin to delineate their sources and respective thermal maturity. The crude oil samples are divided into two main families (A and B) based on differences in source inputs and thermal maturity. Using source specific parameters including pristane/phytane (Pr/Ph), hopane/sterane, dibenzothiophene/ phenanthrene (DBT/P), Pr/n-C17 and Ph/n-Cl8 ratios and the distributions of tricyclic and tetracyclic terpanes, family B oils are ascribed a marine source rock deposited under sub-oxic conditions, while family A oils have a more terrigenous source affinity. This genetic classification is supported by the stable carbon isotopic compositions (d13C) of the n-alkanes. Using biomarker maturity parameters such as the abundance of Pr and Ph relative to n-alkanes and the distribution of sterane and hopane isomers, family A oils are shown to be more thermally mature than family B oils. The contrasting maturity of the two families is supported by differences between the stable hydrogen isotopic compositions (dD) of Pr and Ph and the n-alkanes, as well as the d13C values of n-alkanes in their respective oils.