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The use of mineral diagenetic indices and organic matter maturity is useful for reconstructing the evolution of sedimentary basins and critical assessments for potential source rocks for petroleum exploration. In this study, the relationship of clay mineral diagenesis and organic matter thermal indices (Rock-Eval Tmax) and calculated vitrinite reflectance (%Ro) were used to constrain the maximum burial depths and temperatures of three distinct intervals within the northern Permian Basin, USA. X-ray diffraction of clay fractions (&lt, 2 &micro, m) consists of illite, chlorite, and illite-smectite intermediates. Primary clay mineral diagenetic changes progressively increase in ordering from R0 to R1 I-S between 2359.5 and 2485.9 m and the appearance of chlorite at 2338.7 m. Rock-Eval pyrolysis data show 0 to 14 wt% TOC, HI values of 40 to 520 mgHC/g TOC, and S2 values of 0 to 62 mg HC/g, with primarily type II kerogen with calculated %Ro within the early to peak oil maturation window. Evaluation of the potential for oil generation is relatively good throughout the Tonya 401 and JP Chilton wells. Organic maturation indices (Tmax, %Ro) and peak burial temperatures correlate well with clay mineral diagenesis (R0&ndash, R1 I-S), indicating that maximum burial depths and temperatures were between 2.5 and 4 km and &lt, 100 &deg, C and 140 &deg, C, respectively. Additionally, the use of clay mineral-derived temperatures provides insight into discrepancies between several calculated %Ro equations and thus should be further investigated for use in the Permian Basin. Accordingly, these findings show that clay mineral diagenesis, combined with other paleothermal proxies, can considerably improve the understanding of the complex burial history of the Permian Basin in the context of the evolution of the southern margin of Laurentia.

The verdine facies clay assemblages are regularly encountered in shallow marine sediments of equatorial latitudes where Fe of terrigenous origin is readily available. There, the 7 A Fe-rich green clay (odinite) of syn-sedimentary origin commonly occurs. Previous findings suggested that odinite serves as a precursor of diagenetic chlorite whose importance in porosity conservation has been widely acknowledged. The investigation of Fe-rich clays is, therefore, helpful to constrain the specific conditions and mechanisms, which give rise to chlorite growth, thus illuminating the history of early burial. In this contribution, we studied Cretaceous sediments from the Gabon coast where multiple sedimentary basins came into existence prior, during and after the opening of the South Atlantic. Analyzed core is siliciclastic and petroleum bearing stemming from the fluvio-lacustrine-deltaic environment recovered from depths of ∼1500 m TVD. Electron micro-beam investigation coupled with X-ray diffraction on the clay fraction and spectra fitting revealed odinite, interstratified odinite-chlorite (O-C), and to a lesser extent, illite-chlorite-smectite (I-C-S) and illite-smectite occur as grain coatings and pore-filling phases with a characteristic honeycomb texture. Embryonic chlorite emerges at the contact of odinite and O-C flakes as a particulate authigenic mineralization. Formed from aluminosilicate and Fe-oxyhydroxide debris at sediment-water interface, odinite becomes intrinsically unstable, possibly due to the activity of Fe-reducing bacteria or decaying organic matter creating a prevalently reducing environment that promotes Fe reduction. Such condition facilitated a two-step chlorite growth, which first included a partial chloritization of odinite through the in situ solid-state transformation of 7 A to 14 A layers. Then, with increasing burial, at peak diagenetic conditions (50 °C, ∼1.5 km depth), odinite and O-C both recrystallized to form eogenetic chlorite most likely following the Ostwald ripening mechanism.

Highlights • Coupled geomicrobiology and geomechanics to investigate alterations in shales. • Microbial process can alter the mechanics, mineralogy, and microstructure of shales. • Biogeomechanical alterations reduced permeability by 93% and porosity by 38%. • Microfractures in shales can be sealed during biogeomechanical alterations. • Biogeomechanical alterations can enhance CO2 storage security and caprock integrity. Shales have been a major focus of the energy industry over the past few decades. Recently, there is a paradigm shift in the energy industry to low-carbon solutions, such as carbon capture and storage (CCS), to mitigate global warming caused by carbon footprint. The problem of long-term safe and efficient geological CO2 storage (GCS) and caprock integrity are some of the major challenges impeding large-scale CCS application. Here, we investigated how localized and bulk biogeomechanical alterations could potentially impact caprock integrity and CO2 storage in depleted shale reservoirs. We cultivated the shale core samples (containing both artificial-induced and pre-existing natural fractures) with a cultured microbial solution at specific temperature, time, and growth conditions. Subsequently, we obtain the properties of the fractured shale rock samples impacted by this microbial process. We investigate the impact of the mechanical responses due to the microbial process, on the long-term integrity and storage potentials of CO2 in shale reservoirs. Our results suggest that in Eagle Ford, Marcellus, and Niobrara shale formations, microbially-altered local and bulk mechanical properties can enhance the long-term caprock integrity and CO2 storage security by: (1.) Increasing the localized (+19% unconfined compressive strength, −20% Poisson’s ratio, +35% fracture toughness) and bulk (+50% unconfined compressive strength, −13% Poisson’s ratio) mechanical integrity; (2.) Decreasing permeability (−93%) and porosity (−38%); (3.) Altering the clay mineral content (−56%), calcite content (+21%), and morphology; (4.) Occluding microfractures; and (5.) Mitigating any potential leakage to the atmosphere through the caprock. This study considers the heterogeneity of shales, and provide valuable insights and viable assessment in solving the long-term GCS application in depleted hydrocarbon reservoirs.

The Avalon Zone hosts well-preserved examples of high- and low-sulfidation epithermal Au-Ag mineralization and associated phyllosilicate alteration. Using examples from the Hope Brook and Hickey's Pond high-sulfidation systems (HSS) and the Heritage low-sulfidation system (LSS), this study presents new data on the mineralogical and chemical characterization of phyllosilicates associated with epithermal Au-Ag deposits. Electron probe microanalysis and X-ray diffraction studies revealed that the HSS examples contain Fe muscovite ((K0.62–0.79Na0.10–0.37Ca0.00–0.01)Al1.31–1.72(Mg0.01–0.08Fe0.05–0.19)(Al1.00–1.24Si2.76–3.00O10)(OH)2), paragonite ((K0.05–0.30Na0.78–1.02Ca0.00–0.01)Al1.66–1.84(Mg0.00–0.01Fe0.02–0.04)(Al1.01–1.11Si2.89–2.99O10)(OH)2), Al clinochlore ((Mg2.42–2.65Fe1.62–1.78)(Si2.57–2.69Al1.31–1.43O10)(OH)8), pyrophyllite, kaolin minerals, illite-smectite (I-Sme) and chlorite-smectite (C-Sme). Conversely, the LSS examples contain Fe-Mg muscovite ((K0.44–0.76Na0.00–0.02Ca0.00–0.01)Al1.55–1.82(Mg0.17–0.31Fe0.05–0.12)(Al0.55–0.71Si3.29–3.45O10)(OH)2), Al clinochlore ((Mg2.17–2.56Fe1.59–2.01)(Si2.71–2.92Al1.08–1.29O10)(OH)8), and I-Sme and C-Sme intermediates. Chlorite geothermometry indicated that HSS and LSS assemblages crystallized at average temperatures of 261 °C and 145 °C, respectively. Mica and chlorite from HSS and LSS are defined by Tschermak substitution and high-temperature polytypism (2M1 and IIb, respectively). In the HSS examples, one or more pulses of hot, acidic fluid reacted with host rocks generating an envelope of advanced argillic alteration (Fe-Ms, Kln, Pg, Prl) around a vuggy silica core. This is bounded by a zone of argillic alteration (Fe-Ms, Kln), with sericitic/chloritic alterations (Fe-Ms, Al-Clc) developed in distal parts of the systems. In the LSS, near-neutral hydrothermal fluids led to the formation of broad phyllic/chloritic zones (Fe-Mg Ms and Al-Clc). A low temperature overprint with 1M mica, Ib clinochlore ((Mg2.48–2.74Fe1.58–1.73)(Si3.05–3.15Al0.85–0.95O10)(OH)8), kaolinite and Sme-poor I-Sme and C-Sme is attributed to late waning stage hydrothermal activity and/or weathering. A close paragenetic link was established between Fe-Mg muscovite and Ag mineralization at Heritage, as well as between Fe-Mg muscovite and bladed calcite, suggesting boiling as the precipitation mechanism. The present study provides guidance on how phyllosilicate assemblages have the potential to discern HSS versus LSS mineralization during early prospection in terranes with limited exposure, and to contribute to the reconstruction of their hydrothermal record.

Miocene tuffs preserved in argillaceous sediment interbedded with lacustrine successions are commonly encountered throughout the Dinarides Lake System (DLS) in south-eastern Europe. In this contribution the volcanic glass degradation and co-genetic Mn-Fe precipitation were studied in a 14.68 Ma felsic tuff from DLS Livno-Tomislavgrad Basin. Microbial activity has been involved in both reactions thus adding the interest of revealing effects of biotic and abiotic processes taking place during tuff eogenesis. X-ray diffraction and electron microbeam analysis with energy-dispersive X-ray spectroscopy revealed the pitting or granular structures developed at glass rims along with smectite flakes protruding from a degrading glass. Mn-Fe mineralization emerges in the form of Mn-Fe coatings, an initial step to micronodule formation, where traces of biogenetic influence included a high content of phases rich in structural Mn (IV) (i.e., ranci&eacute, ite and jacobsite) and presence of microbial microfossils. Co-genetic ties between glass degradation and Mn-Fe precipitation were established through the report of dioctahedral smectite formed out of altered glass, which then served as nuclei of the ongoing biotic and abiotic Mn-Fe mineralization. These processes manifest on a continuous involvement of microbial life in the course of eogenesis of pyroclastic material in lacustrine environments.

In the southern U.S. states, expansive soils are frequently encountered, presenting an important hazard in geotechnical engineering. This research relies on mineralogical and geochemical clues to explain the swelling behavior of smectite-rich, high-plasticity soils, documented in a series of geomechanical swelling tests that were performed on the soils stabilized with the metakaolin (MKG) and fly ash (FAG) based geopolymers. These geopolymers were mixed with the soil at several concentration levels. The lowest swelling percentage was shown to correspond to the sample stabilized with 12% FAG and was attributed to the neoformation of calcium silicate hydrates that acted as a cementitious material, preventing the soil from expanding by occupying the pore space, thus binding the clay particles together. Conversely, the 12% MKG-stabilized soil exhibited enormous expansion, which was explained by montmorillonite swelling to the point that it gradually began to lose its structural periodicity. The relatively high abundance of the newly formed feldspathoids in MKG-treated samples is believed to have greatly contributed to the overall soil expansion. Finally, the cation exchange capacity tests showed that the percentage of Na+ and Ca2+, as well as the pH value, exercised strong control on the swelling behavior of smectitic soils.