Potential source rocks, organic geochemistry and thermal maturation in the southern depocenter (Kipourio–Grevena) of the Mesohellenic Basin, central Greece

The study area is the southern depocenter (depth > 4200 m) of the Mesohellenic Basin which extends between Kipourio and Grevena, central Greece. The Mesohellenic Basin is a Middle-Tertiary intramontane basin developed within the Hellenide orogen. Previous studies have focused on the depositional environments, configuration and hydrocarbon potential of the basin. In this paper we present additional geochemical and petrographic data from outcrop samples of the basin's southern depocenter, which is considered the most promising area, in terms of hydrocarbon prospectivity. A total number of thirty six samples were analysed: Rock-Eval pyrolysis, maceral analysis, vitrinite reflectance and thermal alteration index, bitumens extraction, liquid chromatography, and GC-MS. The samples were collected from deltaic deposits and submarine fan sediments of Late Eocene to Late Oligocene age. The TOC values of the analysed samples range between rich and very rich and the organic matter consists mainly of type III kerogen and the organic matter consider to be predominately gas prone. The thermal maturity assessed from T_max and vitrinite reflectance shows an immature stage of the organic matter along with the presence of layers having reached the very early mature stage. Vitrinite reflectance measurements and maturity calculations (applying the Lopatin modeling), reveal that the lower part of the depocenter sediments falls within the ‘oil window’. The extractable organic matter (EOM) (mg bitumens/g TOC) indicate the existence of samples (from deltaic deposits) with high ratio of transformation (EOM) (> 100 mg bitumen/g TOC). The GC and GC-MS analyses of the biomarkers indicate mainly the occurrence of terrestrial organic matter reflecting oxidizing conditions and both immature and very early mature stages. The results of the Rock-Eval pyrolysis and the distribution of the isoprenoids support the assumption of the input of an organic matter mixture.     

Organic geochemistry and petrography of Lower Cretaceous Wealden black shales of the Lower Saxony Basin: The transition from lacustrine oil shales to gas shales

Ninety-seven Wealden black shale samples from three wells in the Lower Saxony Basin have been studied by organic geochemical and organic petrographical methods to determine their maturity, organic facies and depositional environment. The maturities of the three wells range from early mature (Ex-A), late to postmature (Ex-C) to overmature (Ex-B) as determined by vitrinite reflectance measurements, diamondoid ratios and other geochemical maturity parameters. Ex-C and Ex-B show distinct petrographic features related to oil generation and migration. In particular, the occurrence of dispersed solid bitumen replacing initial type I kerogen suggests a formerly active petroleum system. Structural and textural differences between early mature alginites and solid bitumen in postmature to overmature samples show an alteration of the pore system with increasing maturity. A freshwater depositional environment is indicated by widespread occurrence of botryococcus algae and other small alginite particles predominating in the immature well. These alginites are absent in the more mature gas shales of wells Ex-C and Ex-B. Geochemical evidence of algae and phytoplankton in general is provided by numerous biomarker parameters, while the occurrence of β-carotane in some samples indicates events of increased salinity, although no hypersaline conditions are inferred due to very low gammacerane indices. Increased amounts of vitrinite and inertinite in samples of Ex-B suggest locally significant terrigenous input of organic matter for some periods during Wealden Shale deposition. High sulfur/organic carbon ratios provide evidence for sulfate rich waters and (partly) anoxic bottom water conditions. While the lower mature lacustrine source rocks generate paraffinic/waxy oils, gas and condensates are produced at post-mature stages. Furthermore, maturity distribution maps from 3D numerical petroleum systems modeling reveal substantial differences in respect to petroleum generation.     

Geochemical features of re-deposited organic matter occurring in fluvioglacial sediments in the Racibórz region (Poland): A case study

The erosion of rocks rich in organic matter typically leads to the complete mineralization of the organic material. However, in some cases, it is re-deposited to become a part of sediments once more. This process should be considered to be a part of global carbon cycle, possibly much more significant than assumed to-date. The research presented here aims to characterize re-worked organic matter occurring in post-glacial sediments of southern part of Poland, in the Oder river valley (the Racibórz town region, Miocene, Pleistocene and Holocene age). Organic substances extracted from the sediments originated from organic matter that had resided in rocks eroded by glaciers. Sediments were sampled in two boreholes which sediments were correlated. Sediments were extracted and extracts analyzed with gas chromatography-mass spectrometry (GC-MS) to assess distributions of biomarker groups. Organic matter of selected samples was pre-concentrated and analyzed with Py/GC-MS. In the extracts several biomarker parameters of source/environment and thermal maturity were calculated. Organic substances in the investigated sediments come from variable re-deposited organic matter occurring in rocks eroded by glaciers. Three main parent types of re-deposited organic material are identified showing variable geochemical features: 1) organic matter of recent or almost recent age being the source of polar labile compounds; probably formed in situ, 2) re-deposited organic matter of the middle diagenesis showing features similar to lignites (huminite reflectance Rf ~ 0.25–0.35%) deriving from angiosperm remains, mainly monocotyledons and to the lower extend also deciduous trees, 3) re-deposited organic matter at the middle catagenesis (Rf ~ 0.65–0.75%) being the source of most of aromatic hydrocarbons and biomarkers such as steranes, hopanes of the more thermally advanced distribution type. Its geochemical properties and assumed directions of sediment transport indicate bituminous coals of Upper Silesian Coal Basin together with coaly shales as a possible source of this organic matter. Such mixed origin of organic matter caused large discrepancies in values of thermal maturity parameters depending on input from the particular sources and occurrence both geochemical biomarkers and their biochemical precursors in the same samples.     

Application of organic petrology and geochemistry to coal waste studies

Coal wastes produced during mining activities are commonly deposited in nearby dumps. These wastes mostly composed of minerals and variable amounts (usually 20-30%) of organic matter start to weather immediately after deposition. Oxidation of the organic matter can lead to self heating and self combustion as a result of organic and mineral matter transformations. The degree of alteration depends on the properties of the wastes, i.e., the maceral and microlithotype composition of the organic matter and its rank.Alteration of wastes also depends on the heating history, i.e., the rate of heating, final heating temperature, duration of heating, and the degree of air access. Although air is probably necessary to initiate and drive the heating processes, these usually take place under relatively oxygen depleted conditions. With slow heating, color of organic matter particles changes, irregular cracks and oxidation rims develop around edges and cracks, and bitumen is expelled. As a result, massive and detritic isotropic and strongly altered organic matter forms. On the other hand, higher heating rates cause the formation of devolatilization pores, oxidation rims around these pores and along cracks, vitrinite-bands-mantling particles, and bitumen expulsions.Organic compounds generated from the wastes include n-alkanes, iso-alkanes, alkylcyclohexanes, acyclic isoprenoids, mainly pristane, phytane and, in some cases, farnesane, sesquiterpanes, tri- and tetracyclic diterpanes, tri- and pentacyclic triterpanes, and steranes, polycyclic aromatic hydrocarbons (mostly with two- to five rings, rarely six rings), and phenols. The compounds formed change during the heating history. The fact that phenols are found in dumps where heating has not yet been completed, but are absent in those where heating ceased previously suggests the presence of water washing. The organic compounds formed may migrate within the dumps. However, when they migrate out of the dumps, they become a hazard to environment.This paper is a review on transformations of organic matter (both maceral composition and reflectance and chemical composition) in coal wastes deposited in coal waste dumps. Immediately after deposition the wastes are exposed to weathering conditions and sometimes undergo self heating processes.     

Characteristic of homodrimane and maturity of organic matter in the low mature source rocks

Bicyclic sesquiterpenoids are mostly used to illustrate the origins of organic matter and genetic types of crude oil presently.In this paper,the relationship between distributions and compositions of C16 homodrimane in immature to mature source rocks and evolution of organic matter was studied,and the correlation between C16 homodrimane at immature to low mature stages and thermal evolution of organic matter was analyzed.The results show that in terrestrial facies depositional system,the ratio of 8α(H)-homodrimane to 8β(H)-homodrimane has a high sensitivity about the maturity’s minor changes at immature to low mature stages.It is found that when the vitrinite reflectance R0<0.7%,the ratio significantly decreases with increasing burial depth or maturity.This kind of phenomenon reveals that these parameters may be the useful maturity indicators for determining the relative maturation of organic matter at immature to low mature stages,and have certain practical value in biogeochemical and en- vironmental geochemical research on low mature oil and gas.     

三塘湖盆地中生界烃源岩有机质成熟度的确定

运用镜质组反射率、袍子体荧光参数、生物标志物参数详细研究了三塘湖盆地中生界烃源岩的有机质热演化特征及演化阶段。研究表明镜质组反射率是该区有机质热汪化最可靠听成熟度参数，孢子体荧光参数是重要的热演化指标，生物标志物参数是有效的热演化指标。三塘湖盆地有机质总体热演化水平较低，且在横向和纵向上存在明显的差异。该区的有机质热演化具有明显的阶段性，运用成熟度参数将其划分为未成熟和成熟两个阶段。     

Biomarker transformations as constraints for the depositional environment and for maximum temperatures during burial of Opalinus Clay and Posidonia Shale in northern Switzerland

Samples from two argillaceous formations (Opalinus Clay and Posidonia Shale) of near-identical maturity from northern Switzerland were subjected to a geochemical characterisation of organic matter and to confined-system pyrolysis experiments. Throughout the study area, the characteristics of organic matter are similar, indicating a spatially homogeneous sedimentary facies. Posidonia Shale contains marine organic matter deposited in a reducing environment, while a predominantly terrigenous source and a more oxidising environment of deposition was identified for Opalinus Clay. In the western and central parts of the study area, organic maturity is close to the onset of oil generation. In the easternmost part, a higher maturity has been reached due to a deeper burial below thick Tertiary Molasse deposits.Isothermal pyrolysis experiments were conducted at temperatures between 250 and 390 °C over 24 h. Bitumen yields increase along similar pathways for both Opalinus Clay and Posidonia Shale, but the maximum values are displaced by 10–20 °C. Data pertaining to maturity were determined from GC–MS analyses of saturated hydrocarbons, and specific attention was given to C₂₉-sterane and C₃₂-hopane isomerisation ratios. The evolution of these parameters with rising temperature is slightly different in the two formations, which is attributed to the contrasting organic facies. The pyrolysis data, together with literature data from natural basins, were used to calculate kinetic parameters for C₂₉-sterane and C₃₂-hopane, assuming a single-step isomerisation scheme according to the Arrhenius law. The resulting values based on pyrolysis data alone are very similar to those based on the combination of pyrolysis and natural data. Activation energies are similar in both formations, while the frequency factors are up to one order of magnitude higher for Posidonia Shale when compared to Opalinus Clay. For the Benken site, maximum temperature during Cretaceous burial was calculated on the basis of the kinetic data, using the TTI approach. The resulting temperatures of 75–80 °C are 5–10 °C below those derived in the literature from apatite fission-track analysis, vitrinite reflectance and basin modelling.     

The analysis of oil trapped during secondary migration

During secondary migration, there is an opportunity for oil to be trapped as fluid inclusions (FIs) within framework grains such as quartz and within diagenetic cements that have a crystalline structure. Oil saturation on migration pathways remains relatively low, so typically fewer oil inclusions get trapped compared with samples from an oil column. Geochemical analysis of the much smaller amounts of inclusion oil present in samples from interpreted oil migration pathways has been attempted for two samples from the Champagny-1 and Delamere-1 wells in the Vulcan Sub-Basin, northern offshore Australia. A combination of petrographic analysis, bulk geochemical inclusion analysis and log evaluation confirmed that both samples were from oil migration pathways. Despite the small number of oil inclusions, reliable geochemical data were acquired from both samples that were significantly above the levels detected for the system and outside-rinse blanks. The FI oil trapped on the interpreted oil migration pathway in Champagny-1 was generated from clay-rich marine source rock with little terrigenous organic matter input. It was generated at peak oil window maturity and correlates best with oils derived from the Late Jurassic Lower Vulcan Formation. In contrast, the Delamere-1 FI oil contains evidence of greater input of terrigenous organic matter and was generated at early oil window maturity. This FI oil also contains a signature of a biodegraded component, which could have been generated either from the Middle Jurassic Plover Formation, or from an older source rock. These data indicate that it is feasible to geochemically map migration pathways across prospects or basins, and to analyse palaeo-oil compositions in oil zones where the few inclusions get trapped. This also suggests that the few oil inclusions that sometimes occur in Proterozoic or Archaean rocks may be analysable in the future, which would provide relatively pristine and robust data on the composition and diversity of Earth’s early biosphere.     

Electron spin resonance of stabilized free radicals in sedimentary organic matter

Electron spin resonance (ESR) is evaluated as a method to study the thermal degradation of sedimentary organic matter which consists mainly of kerogen. Whole rock and separated kerogen samples were pyrolysed stepwise (ambient to 700°C at 50°C increments), extracted and analysed for elemental composition and ESR spectra at each step. Whole rock samples give rise to complex spectra which include those of paramagnetic metals and are therefore unsuitable in most cases for this purpose.The ESR parameters g value, ΔH and N_g differ for different types of immature organic matter. An increase in N_g,shift of g value to 2.0026–2.0028 and reduction in h are the main trends during pyrolysis and in natural heating of sedimentary organic matter.The peak generations of liquid and gaseous hydrocarbons coincide with maxima of free radical density. ESR spectroscopy in combination with complementary geochemical characterization of the sedimentary organic matter can serve to indicate maturity with respect to peak oil-gas generation.     

CRUSTAL GRANITOIDS

Eocene organic-rich sediments are widespread in the Amasya region of north-central Turkey and have been studied in outcrop. Detailed data from thick Eocene sediments (Derealan Formation) made it possible to construct an organic-facies framework using different zonations.

Organic matter is composed predominantly of autochthonous algal and amorphous material, with a minor contribution of allochthonous terrestrial material. Kerogen in the deposits is primarily Type I, as indicated by organic petrographic observations and Rock-Eval data. Total organic-carbon content (TOC) of this deposit decreases from over 54% in limestone and shale to less than 2% in the other deposits of the Derealan Formation. Tmax values vary between 441 ° and 456° C, confirming the increase in maturation trends indicated by vitrinite reflectance data.

Both organic petrographic and geochemical maturation parameters place the Eocene sediments of the Northern Gumushacikoy (Amasya) region within the B organic facies. According to the organic-carbon/sedimentation-rate relationship, the preservation of matter took place under anoxic conditions.     

Petroleum source rocks of the Tarfaya Basin and adjacent areas, Morocco

This work characterizes the source rock potential of the Tarfaya Basin and enabled us to reconstruct its geochemical history. Outcrop samples covering different stratigraphic intervals, plus the northwestern part of the Zag/Tindouf Basin (Bas Draa area), were analyzed for total organic carbon (C_org) and total inorganic carbon contents and total sulfur content. Rock-Eval analysis and vitrinite reflectance measurements were performed on 56 samples chosen on the basis C_org content. A set of 45 samples were extracted and non-aromatic hydrocarbons were analyzed by way of gas chromatography-flame ionization detection (GC-FID) and GC-mass spectrometry (GC-MS). Non-isothermal open system pyrolysis at different heating rates was applied to obtain kinetic parameters for modelling petroleum generation from four different source rocks.High quality petroleum source rocks with high C_org content and hydrogen index (HI) values were found for samples of Eocene, Coniacian, Turonian and Cenomanian age. Most samples were carbonate rich and organic/sulfur values were high to moderate. Various maturity parameters indicated immature or possibly early mature organic matter. Based on organic geochemical and petrological data, the organic matter is of marine/aquatic origin (Cenomanian) or a mixture of aquatic and terrigenous material (Eocene). The Early Cretaceous interval did not contain high quality source rocks, but indications of petroleum impregnation were found.     

Applications of microscopy to coke making

A Canadian perspective of the petrographic, thermal rheological and grade of metallurgical coals required to make coke with high strength and strength after reaction (CSR) properties is presented. The development of automated microscopic techniques to obtain reproducible and reliable petrographic data to predict coke quality is discussed. The amount of “altered vitrinite” in the microscopic coke textures has been used as a reference to quantifiy in situ coal oxidation. Relationships between coke microscopy, coal petrography and thermal rheological data show that FSI can be used to estimate the amount of oxidized vitrinite plus petrographic inert contents of coal. Plastic temperature ranges determined from microscopic examination of the coal/coke transformations for Appalachian and Canadian coals show that standard thermal rheological tests underestimate the plastic range for high inertinite coals.     

An organic geochemical investigation on organic rich sediments from two Neogene formations in the Klias Peninsula area,West Sabah,Malaysia

Twenty organic rich outcrop samples from the Belait and Setap Shale formations in the Klias Peninsula area, West Sabah, were analysed by means of organic petrology and geochemical techniques. The aims of this study are to assess the type of organic matter, thermal maturity and established source rock characterization based primarily on Rock-Eval pyrolysis data. The shales of the Setap Shale Formation have TOC values varying from 0.6 wt%–1.54 wt% with a mean hydrogen index (HI) of 60.1 mg/g, whereas the shal...     

Evolution of polycyclic alkanes in the Espirito Santo Basin

The distributions of polycyclic alkanes were monitored in a Neocomian sequence (well 1-ESS-34) from the Espirito Santo Basin, southeast Brazil. The profiles included, apart from regular hopanes, significant concentrations of 18α(H), 28,30-bisnorhopane and subordinate amounts of gammacerane. Sterane concentrations, normally with hopane/sterane <5, were compatible with other geochemical data indicating a predominantly planktonic/microbial source of the deposited organic matter. Sample maturities ranged from very immature to the onset of oil generation, allowing biomarker distributions to be followed along a broad maturation range. The ability of certain molecular ratios (e.g. C₂₇ 17α(H)/17β(H)hopanes) to reflect a maturity sequence with depth in the closely-spaced strata of the immature upper levels (Jiquiá Stage) showed the value of molecular techniques over classical geochemical methods (e.g. vitrinite reflectance) for the study of immature sequences. The presence in the oils of southern Espirito Santo of 28,30-bisnorhopane, gammacerane and methyl steranes in similar concentrations as in extracts of the deepest levels of the 1-ESS-34 well qualify the Jiquia Stage as the probable source rock of oils accumulated in the basin.     

武钢使用配煤组成与胶质层粘结系数关系

近几年来,随着钢铁业的发展,工业用煤需求量愈来愈大,但煤质波动较大,致使炼焦质量在同一配比条件之下的配煤也产生不同程度的差异,使焦炭质量明显下降,其Ｍ４０为７６％～７８％,Ｍ１０为８－４％～９－０％。而焦炭的热稳定性,则是导致高炉高产顺行的主要因素之一。目前,武钢高炉碱负荷大约为７～８ｋｇｔ铁,如此高的碱负荷条件下焦炭在高炉中的热稳定性势必受其干扰。十多年来,我们在试验室及跟踪生产研究表明,焦炭在无碱或低碱（＜２ｋｇｔ铁）害的高炉中,焦炭热强度有明显差异。武钢目前生产所用焦炭,在无碱害、１１…     

The Soil Geochemical Atlas of Portugal: Overview and applications

The continental area of Portugal is now entirely covered by a soil geochemical survey (1 site/135 km²), taking as the sampling media topsoils (upper mineral horizons, A) and organic horizons (humus, O). Standard methods for sampling, sample preparation and analysis were used in order to achieve high quality and consistent data. Each sample was analyzed for 32 chemical elements, pH, electrical conductivity and organic matter content.The main purpose of the survey was to obtain baseline levels for various chemical elements. The compilation of all data (nearly 45,000 individual data) in an organised way, led to the production of the first Soil Geochemical Atlas of Portugal. In this Atlas it is possible to find for each chemical element a set of information statistics (basic statistical parameters, boxplots, cumulative frequency curves, etc.), maps of spatial distribution, among other information of geochemical and environmental interest. This paper gives an overview of the Soil Atlas and examples of application. The data were used to calculate reference values for 9 elements of environmental importance and to obtain empirical formulae allowing the estimation of elements in the coarse fraction of soils (< 2.00 mm) from known concentration in a finer fraction (< 0.18 mm).     

In situ and laboratory investigation of the alteration of Boom Clay (Oligocene) at the air–geological barrier interface within the Mol underground facility (Belgium): Consequences on kerogen and bitumen compositions

The Boom Clay formation (Oligocene) is studied as a reference host rock for methodological studies on deep geological disposal of radioactive waste. During excavation of galleries within the Clay formation (HADES underground research facility, Mol, Belgium), the physico-chemical conditions are significantly modified as an air–clay interface is created. In order to study the long-term impact of the air–clay contact on the organic matter contained in the Boom Clay, two types of samples were studied: (1) a reference series of clay samples having been in contact with the atmosphere of the HADES gallery for increasing times up to several years and (2) unaltered clay samples submitted to artificial oxidation in a ventilated oven at 80 °C. The evolution of geochemical data of the two series was compared using Rock-Eval pyrolysis, GC–MS and size exclusion chromatography. The organic matter of the unaltered clays sampled in the HADES galleries is dominated by type III kerogen (terrestrial) with some contribution of type II (marine) and is thermally immature. The evolution of geochemical parameters during air alteration for the two series are very similar. They show progressive oxidation of kerogen accompanied by the release of bitumen enriched in low molecular weight constituents. Molecular analysis evidences the presence of a complex mixture of aliphatic and aromatic O-bearing compounds, inherited from the degradation of kerogen as well as from the clay catalyzed oxidation of the bitumen. These results show that (1) air oxidation is a major process in the in situ alteration of the organic matter of Boom Clay within the HADES galleries, (2) laboratory oxidation experiments at 80 °C yield similar results as in situ air alteration of Boom Clay and (3) artificial air oxidation may be used to assess the long term exposure of the organic matter to air.     

Organic geochemical characteristics and depositional environments of the Jurassic coals in the eastern Taurus of Southern Turkey

In this study, organic matter content, type and maturity as well as some petrographic and physical characteristics of the Jurassic coals exposed in the eastern Taurus were investigated and their depositional environments were interpreted.The total organic carbon (TOC) contents of coals in the Feke–Akkaya, Kozan–Gedikli and Kozan–Kizilinc areas are 24.54, 66.78 and 49.15%, respectively. The Feke–Akkaya and Kozan–Kizilinc coals have low Hydrogen Index (HI) values while the Kozan–Gedikli coals show moderate HI values. All coal samples display very low Oxygen Index (OI) values. The Kozan–Gedikli coals contain Type II organic matter (OM), the Feke–Akkaya coals contain a mixture of type II and type III OM; and the Kozan–Kizilinc coals are composed of Type III OM. Sterane distribution was calculated as C₂₇ > C₂₉ > C₂₈ from the m/z 217 mass chromatogram for all coal samples.T_max values for the Feke–Akkaya, Kozan–Gedikli and Kozan–Kizilinc coals are 439, 412 and 427 °C. Vitrinite reflectance values (%R_o) for the Feke–Akkaya and Kozan–Kizilinc coal samples were measured as 0.65 and 0.51 and these values reveal that the Feke–Akkaya and Kozan–Kizilinc coals are at subbituminous A or high volatile C bituminous coal stage. On the basis of biomarker maturity parameters, these coals have a low maturity.The pristane/phytane (Pr/Ph) ratios for the Feke–Akkaya, Kozan–Gedikli and Kozan–Kizilinc coals are 1.53, 1.13 and 1.25, respectively. In addition, all coals show a homohopane distribution which is dominated by low carbon numbers, and C₃₅ homohopane index is very low for all coal samples. All these features may indicate that these coals were deposited in a suboxic environment.The high sterane/hopane ratios with high concentrations of steranes, low Pr/Ph ratios and C₂₅/C₂₆ tricyclic ratios > 1 may indicate that these coals formed in a swamp environment were temporarily influenced by marine conditions.     

Organic matter maturation under the influence of a deep intrusive heat source: A natural experiment for quantitation of hydrocarbon generation and expulsion from a petroleum source rock (Toarcian shale, northern Germany)

Four shallow boreholes were drilled in the Hils syncline, northern Germany, in order to determine quantitatively the amount of hydrocarbons generated and expelled during maturation of a typical kerogen-type-II-bearing source rock. The holes penetrated the carbonceous Lias shales (Posidonia shale, Lower Toarcian) and part of the adjacent Dogger α and Lias δ mudstones. The maturity of the organic matter in the cores recovered ranges from immature (0.48% R̄₀) to overmature 1.45% R̄₀) due to location of the Hils syncline in the vicinity of the Vlotho Massif, which is deep-seated intrusive body. Facies variations of the Lias within the short geographical distances in the study area are negligible.Organic matter mass balance calculations were based on detailed organic geochemical analyses of residual material in the Lias shales (kerogen, bitumen etc.) and on the evidence of a uniform initial composition of these sediments in the study area. Dead carbon determinations supported this latter criterion but were not used as a parameter in the calculations.About 50% of the initial kerogen was transformed into oil, gas and inorganic compounds during the vitrinite reflectance increase from 0.48 to 0.88% R̄_o and only marginally more during the maturity increase from 0.88 to 1.45% R̄_o. Only a small portion of the generated material remained in the source rock even at a relatively early stage of generation (0.68% R̄_o). Expulsion efficiency of oil plus gas reached a value of 86% at the end of the main generation stage (0.88% R̄_o).     

Molecular composition and organic petrographic characterization of Madbi source rocks from the Kharir Oilfield of the Masila Basin (Yemen): palaeoenvironmental and maturity interpretation

The upper part of Madbi Formation organic-rich shale is considered an important regional source rock in the Masila Basin, Yemen. Ten cutting samples from this Upper Jurassic organic-rich shale were collected from wells drilled in the Kharir Oilfield, Masila Basin in order to geochemically assess the type of organic matter, thermal maturity and depositional environment conditions. Results reveal that Upper Jurassic organic-rich shale samples contain high organic matter more than 2.0 wt.% TOC and have very good to excellent hydrocarbon potential. Marine algae organic matter is the main source input for the Upper Jurassic shale sequence studied. This has been identified from organic petrographic characteristics and from the n-alkane distributions, which dominated by n-C₁₄-n-C₂₀ alkanes. This is supported by the high value of the biomarker sterane/hopane ratio that approaches unity, as well as the relatively high C₂₇ sterane concentrations. A mainly suboxic depositional environment is inferred from pr/ph ratios (1.75–2.38). This is further supported by relatively high homohopane value, which is dominated by low carbon numbers and decrease towards the C₃₅ homohopane. The concentrations of C₃₅ homohopane are very low. The depositional environment conditions are confirmed by some petrographic characteristics (e.g. palynofacies). Detailed palynofacies analysis of Madbi shales shows that the Madbi shale formation is characterised by a mix of amorphous organic matter, dinoflagellates cysts and phytoclasts, representing a suboxic, open marine setting. The Upper Jurassic marine shale sequence in the Masila Basin is thermally mature for hydrocarbon generation as indicated by biomarker thermal maturity parameters. The 22 S/22 S + 22R C₃₂ homohopane has reached equilibrium, with values range from 0.58 to 0.62 which suggest that the Upper Jurassic shales are thermally mature and that the oil window has been reached. 20 S/(20 S + 20R) and ββ/(ββ + αα) C₂₉ sterane ratios suggest a similar interpretation, as do the moretane/hopane ratio. This is supported by vitrinite reflectance data ranging from 0.74% to 0.90%Ro and thermal alteration of pollen and spore. The thermal alteration index value is around 2.6–3.0, corresponding to a palaeotemperature range of 60–120°C. These are the optimum oil-generating strata. On the basis of this study, the Madbi source rock was deposited under suboxic conditions in an open marine environment and this source rock is still within the oil window maturity range.