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Abstract Sedimentary basins containing igneous intrusions within sedimentary reservoir units represent an important risk in petroleum exploration. The Upper Triassic to Lower Jurassic sediments at Wilhelmøya (Svalbard) contains reservoir heterogeneity as a result of sill emplacement and represent a unique case study to better understand the effect of magmatic intrusions on the general burial diagenesis of siliciclastic sediments. Sills develop contact metamorphic aureoles by conduction as presented in many earlier studies. However, there is significant impact of localized hydrothermal circulation systems affecting reservoir sediments at considerable distance from the sill intrusions. Dolerite sill intrusions in the studied area are of limited vertical extent (∼12 m thick), but created localized hydrothermal convection cells affecting sediments at considerable distance (more than five times the thickness of the sill) from the intrusions. We present evidence that the sedimentary sequence can be divided into two units: (1) the bulk poorly lithified sediment with a maximum burial temperature much lower than 60–70 °C, and (2) thinner intervals outside the contact zone that have experienced hydrothermal temperatures (around 140 °C). The main diagenetic alteration associated with normal burial diagenesis is minor mechanical plastic deformation of ductile grains such as mica. Mineral grain contacts show no evidence of pressure dissolution and the vitrinite reflectance suggests a maximum temperature of ∼40 °C. Contrary to this, part of the sediment, preferentially along calcite cemented flow baffles, show evidence of hydrothermal alteration. These hydrothermally altered sediment sections are characterized by recrystallized carbonate cemented intervals. Further, the hydrothermal solutions have resulted in localized sericitization (illitization) of feldspars, albitization of both K-feldspar and plagioclase and the formation of fibrous illite nucleated on kaolinite. These observations suggest hydrothermal alteration at T > 120–140 °C at distances considerably further away than expected from sill heat dissipation by conduction only, which commonly affect sediments about twice the thickness of the sill intrusion. We propose that carbonate-cemented sections acted as flow baffles already during the hydrothermal fluid mobility and controlled the migration pathways of the buoyant hot fluids. Significant hydrothermally induced diagenetic alterations affecting the porosity and hence reservoir quality was not noted in the noncarbonate-cemented reservoir intervals. Graphical abstract Highlights • Diagenesis in the Upper Triassic-Lower Jurassic sediments of Wilhelmøya. • Sill-induced diagenesis observed considerably further away than expected by conduction only. • Hydrothermal alteration observed locally without affecting overall reservoir quality. [ABSTRACT FROM AUTHOR]

Abstract In order to better predict the petrophysical properties of the tight sandstone reservoirs in the Upper Triassic Yanchang Formation, Ordos Basin, China, the nature of the diagenetic system involved was investigated using a suite of petrographic and geochemical techniques including thin section and X-Ray Diffraction analysis, scanning electron microscopy, MAPS mineralogy, Cathodeluminescence, electron probe microanalysis and fluid inclusion analysis on a set of selected tight sandstone samples. The sandstones investigated are texturally mature but compositionally immature with an average framework grain composition of Q 32 F 41 L 27. Authigenic quartz, calcite, and chlorite coatings are the major cements, while feldspars are partially dissolved. Two groups of quartz cement are present in the tight sandstone reservoirs. Smectite to illite conversion provided silica source for the first group of quartz overgrowth (Qo-I), while the silica source for the second quartz overgrowth (Qo-II) was mainly originated from feldspar dissolution. Calcite cements consist of two types, namely Ca-I and Ca-II. The Ca-I calcite cement contains no chlorite coatings and have higher concentrations of Fe2+ and Mg2+, whereas the Ca-II calcite cement developed over the chlorite coatings. Plagioclase dissolution appears to be always accompanied by calcite cementation, while K-feldspar albitization forms euhedral albite locally. The burial diagenesis processes were, in most cases, not episodic but occurred as slow adjustments in response to increased burial depths and temperatures. In all the studied diagenetic minerals, elemental distributions appear to be strictly constrained by the interaction of authigenic minerals involved, indicating that the chemical reactions during the diagenesis comply well with the general principle of mass balance. The diagenesis in the Upper Triassic Yanchang Formation tight sandstones was thus mainly developed in a closed geochemical system, where mineral dissolution and precipitation are approximately balanced, and diagenetic fluids were not affected by external sources significantly. Mechanical compaction has played a more important role in destroying the primary porosities of the Upper Triassic Yanchang Formation than the cementation. Highlights • There are two groups of quartz cement in the tight sandstone reservoirs. • Two types of calcite cement are present in the tight sandstone reservoirs. • Diagenesis of the tight sandstone reservoirs occurred in a closed geochemical system. [ABSTRACT FROM AUTHOR]

Understanding diagenetic fluid types and their effects on diagenesis is important to identify the main control factors of reservoir characteristics and predict reservoir sweet spots. Reservoir space destruction caused by strong cementation is notable in the Lower Jurassic Ahe Formation sandstones near the deep-rooted fault (Yiqikelike Fault) in the Kuqa depression. Different authigenic minerals and widely varying cementation contents indicate the complexity of diagenetic fluids. Therefore, we investigated strong cementation using petrographic and geochemical methods, including cathodoluminescence, scanning electron microscopy, laser ablation inductively coupled plasma mass spectrometry, and stable isotope analysis. The contents of authigenic quartz and calcite increased as they approached the deep-rooted fault, with maximum concentration of quartz and calcite of up to 8.73% and 8.92%, respectively. Abnormally high homogenization temperatures of the fluid inclusions were observed in the quartz overgrowth, one of which reached 156 °C. In calcite, the rare earth element Eu exhibited abnormal characteristics, and the carbon isotopes ranged from −8.00‰ to −2.00‰. Therefore, it is likely that deep fluids are involved in reservoir diagenesis near a deep-rooted fault. This study provides a good example of diagenetic evolution in deep sandstone reservoirs and the negative effects of the involvement of deep fluids in diagenetic processes. • The deep fluids were involved in cementation of diagenesis in Jurassic Ahe Formation sandstones near the deep-rooted fault. • The deep fluids provided material source for authigenic quartz and calcite. • The deep fluid is one reason for the difference in diagenesis between the areas near and far from the deep-rooted fault. [ABSTRACT FROM AUTHOR]

Evidences of CO 2 induced diagenesis in the Quantou Formation, Southern Songliao Basin, have been investigated using petrographic analyses, X-ray diffraction, stable isotopes, fluid inclusions and kinetic-thermodynamic modeling. The studied sandstones have two distinct zones based on their mineralogy, one “pristine” being composed of quartz, plagioclase, chlorite, calcite and dolomite, and one “altered” mainly consisting of quartz, illite and illite/smectite, ankerite, and dawsonite. The ankerite/dawsonite and secondary clay-bearing zones are related to the major deep rooted faults in this area. The δ 13 C value of carbonate cements in the altered zone (mainly centered on −0.9‰ to −8.0‰) is higher than that in the “pristine” sediments. We therefore proposed that these zones have experienced CO 2 charged hydrothermal (∼120–140 °C) alteration and with a similar precursor mineral assemblage as in the plagioclase/chlorite rich zones. Kinetic modeling furthermore suggests that the observed alteration must have been under high CO 2 partial pressures, with the closest match between simulations and XRD data found at the highest attempted pressure of 100 bar. The modeling furthermore suggests that using kinetic data from the literature together with reactive surface areas normalized to the surface area of the pores provides good estimates for the alteration of tight sandstones such as the Quantou Fm (∼8% porosity). [ABSTRACT FROM AUTHOR]

The Lower Cretaceous Quantou Formation in the southern Songliao Basin is the typical tight oil sandstone in China. For effective exploration, appraisal and production from such a tight oil sandstone, the diagenesis and reservoir quality must be thoroughly studied first. The tight oil sandstone has been examined by a variety of methods, including core and thin section observation, XRD, SEM, CL, fluorescence, electron probing analysis, fluid inclusion and isotope testing and quantitative determination of reservoir properties. The sandstones are mostly lithic arkoses and feldspathic litharenites with fine to medium grain size and moderate to good sorting. The sandstones are dominated by feldspar, quartz, and volcanic rock fragments showing various stages of disintegration. The reservoir properties are quite poor, with low porosity (average 8.54%) and permeability (average 0.493 mD), small pore-throat radius (average 0.206 μm) and high displacement pressure (mostly higher than 1 MPa). The tight sandstone reservoirs have undergone significant diagenetic alterations such as compaction, feldspar dissolution, quartz cementation, carbonate cementation (mainly ferrocalcite and ankerite) and clay mineral alteration. As to the onset time, the oil emplacement was prior to the carbonate cementation but posterior to the quartz cementation and feldspar dissolution. The smectite to illite reaction and pressure solution at stylolites provide a most important silica sources for quartz cementation. Carbonate cements increase towards interbedded mudstones. Mechanical compaction has played a more important role than cementation in destroying the reservoir quality of the K 1 q 4 sandstone reservoirs. Mixed-layer illite/smectite and illite reduced the porosity and permeability significantly, while chlorite preserved the porosity and permeability since it tends to be oil wet so that later carbonate cementation can be inhibited to some extent. It is likely that the oil emplacement occurred later than the tight rock formation (with the porosity close to 10%). However, thicker sandstone bodies (more than 2 m) constitute potential hydrocarbon reservoirs. [ABSTRACT FROM AUTHOR]

Lamina, a common lithologic unit in shale, is the smallest unit for organic–inorganic fluid–rock interactions. The effects of lamina-scale diagenetic processes are superimposed to exert on lithofacies-scale diagenetic sequences, which further impose on the entire diagenetic system of a shale reservoir. Organic acids from kerogen maturation are indispensable components in diagenetic reaction. However, previous studies mainly focused on low molecular weight (LMW) water soluble acids, few studies have paid attention to the role of high molecular weight (HMW) carboxylic acids dissolved in fluid–rock reactions. Herein, by taking the shale of the seventh member of the Upper Triassic Yanchang Formation in the Ordos Basin, China, as a case study, we investigate the mutual impacts between mineral alteration and HMW organic acid degradation. The characterization is carried out at two scales: lamina-scale (organic-rich clay-rich lamina and organic-lean silty lamina) and lithofacies-scale (shale and sandstone). Integrated analytical techniques (microdrill technique, thin section observation, X-ray diffraction, advanced mineral identification and characterization system, Rock-Eval pyrolysis, Fourier transform ion cyclotron resonance mass spectrometry) are performed. Results show that, in reservoirs of both silty lamina and sandstone, consumption of LMW aqueous acids through mineral transformation reactions promotes the forward evolution of HMW carboxylic acids in the bitumen phase toward decarboxylation or dehydration. During diagenesis, short chain fatty acids (SCFAs) are more easily broken down into small acids and, thus, more susceptible to be consumed. The lamina-scale reservoirs (silty lamina) have the privilege to receive abundant aqueous organic acids to maintain the micro-geochemical environment and progressively boost organic–inorganic fluid–rock interactions. The resultant dissolution pores not only accumulate plenty of bitumen but also an appreciable amount of bitumen dissolved acids. Because of the strong storage capacity of silty lamina within lithofacies-scale source rock (shale), fluids are less readily to expel out to lithofacies-scale reservoir (sandstone). As a result, the sandstone may not receive enough fluids from shale to maintain a consistent diagenetic environment, resulting in the observed discontinuous diagenesis of quartz precipitation transition to quartz dissolution. [ABSTRACT FROM AUTHOR]

The Eocene sandstones in the northern Dongying Sag, Bohai Bay Basin, China, are reservoirs for large accumulations of hydrocarbons. The sandstones are mainly lithic arkoses and feldspathic litharenites, texturally and compositionally immature. These sandstones have a wide range of porosity (0.4–37%) and permeability (0.004–6969 mD) and show an overall decrease in reservoir quality from 1500 m to 5000 m below sea level. The reduction in reservoir quality is a product of several digenetic processes; these include compaction, precipitation of dolomite and calcite in eodiagenetic stage; compaction, feldspar dissolution, precipitation of quartz cements and clays (kaolin and illite) and precipitation of ferrocalcite and ankerite in mesodiagenetic stage. Mineral distribution pattern and isotopic composition suggest carbonate cements in sandstones originate from sources outside the sandstones. Carbonate cementation, together with compaction reduced the sandstones’ porosity and permeability significantly. In a sandstone bed, marginal sandstones with distance to sandstone/mudstone interface less than one meter always have lower porosity than central sandstones. As burial depth exceeds 4000 m, marginal sandstones have very low porosities (<5%), indicating that thin sandstone beds (<2 m) were totally destroyed by cementation and compaction, and only thick sandstone beds (>2 m) can be potential effective reservoirs. Feldspar dissolution and precipitation of clays and quartz cements have little impact on absolute porosity. Mineral distribution pattern and quantitative data show that leached feldspars are the internal source of authigenic quartz and clays in sandstones, and the volume difference between feldspar secondary porosity and related authigenic cements is generally less than 0.25%. However, although there is little or no net import of matter to the sandstones, the pore architecture changes dramatically. Primary macropores are lost as clays and quartz precipitate while the proportion of microporosity increases, occurring mainly between clay crystals. The overall result is that permeability is significantly degraded. [ABSTRACT FROM AUTHOR]

Carbonates are suggested to dissolve rapidly than feldspars by laboratory experiments. Petrography texture of selective dissolution of feldspars in the presence of carbonates, however, is widespread in buried sandstones and even shales, inspiring a revisit to the chemistry of burial secondary pores. Feldspar dissolution, precipitation of secondary minerals (quartz, clays), and carbonate cementation are common chemical reactions in the Eocene sandstones in the northern Dongying Sag. Petrography evidence demonstrates the selective dissolution of feldspars in the presence of carbonate minerals (both detrital and authigenic minerals) in these buried sandstones. The equilibrium constant of calcite leaching reactions is much smaller than that of K-feldspar leaching reactions. Numerical simulations of chemical reactions in K-feldspar-calcite–CO 2 –H 2 O systems utilizing the Geochemist's Workbench 9.0 (GWB) indicate that only a small amount of calcite was dissolved at the onset of simulation processes, while much K-feldspar was dissolved with precipitation of quartz, clays and some calcite for extended periods of time. Precipitation of secondary calcite could also promote feldspar dissolution. Simulation of reactions in a simplified sandstone system with constraints of present-day pore water and partical pressure of carbon dioxide (pCO 2 ) in the northern Dongying Sag indicates that the pore waters are close to equilibrium with calcite. Petrography evidence and modeling results share consistence in confirming that only feldspar could be dissolved extensively, with precipitation of quartz, clays and some carbonate minerals. The organic CO 2 -leaching theory (Schmidt and McDonald, 1979) regarding the dissolution of mainly carbonates and, to a lesser degree, feldspars to form secondary pores has been questioned due to supposed extensive internal consumption of organic CO 2 in source rocks by carbonate minerals. The CO 2 in sandstones and shales and the isotopic composition of CO 2 and carbonate cements in sandstones, however, suggest migration of organic CO 2 from mudstones (even with large amounts of carbonate) to sandstones. Calculations in this study indicate that, with suppression of carbonate dissolution in sedimentary rocks, many secondary pores can be generated in sandstones through selective dissolution of feldspar by organic CO 2 from thermal evolution of organic matter. Selective dissolution of feldspars, rather than carbonates, in sedimentary rocks is then likely a general mechanism to decipher the chemistry of secondary porosity. Other secondary porosity generation mechanisms were also reevaluated with numerical simulations. Results demonstrate that reverse weathering reactions of silicates may take place with increasing of temperatures, but cannot provide enough H + to dissolve carbonates at elevated temperatures. Additionally, cooling of hot fluids can dissolve only insignificant amounts of carbonate unless significant amounts of water are provided. [ABSTRACT FROM AUTHOR]