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NARROW
GeoRef Subject
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all geography including DSDP/ODP Sites and Legs
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Africa
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minerals
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wollastonite group
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framework silicates
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datolite group
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sorosilicates
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ring silicates
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sheet silicates
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sulfates
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realgar (2)
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Primary terms
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absolute age (3)
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Africa
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Madagascar (2)
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Sound speed and refractive index of amorphous CaSiO 3 upon pressure cycling to 40 GPa
Investigation of Physicochemical Changes of Soft Clay around Deep Geopolymer Columns
Ermakovite (NH 4 )(As 2 O 3 ) 2 Br, a new exhalative arsenite bromide mineral from the Fan-Yagnob coal deposit, Tajikistan
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Effect of magnesium on monohydrocalcite formation and unit-cell parameters
Probing the Structure of Melts, Glasses, and Amorphous Materials
Experimental evidence supports early silica cementation of the Ediacara Biota
Biologically mediated silicification of marine cyanobacteria and implications for the Proterozoic fossil record
An evolutionary system of mineralogy. Part I: Stellar mineralogy (>13 to 4.6 Ga)
ABSTRACT Scanning electron microscopy (SEM) has revolutionized our understanding of shale petroleum systems through microstructural characterization of dispersed organic matter (OM). However, as a result of the low atomic weight of carbon, all OM appears black in SEM (BSE [backscattered electron] image) regardless of differences in thermal maturity or OM type (kerogen types or solid bitumen). Traditional petrographic identification of OM uses optical microscopy, where reflectance (%R o ), form, relief, and fluorescence can be used to discern OM types and thermal maturation stage. Unfortunately, most SEM studies of shale OM do not employ correlative optical techniques, leading to misidentifications or to the conclusion that all OM (i.e., kerogen and solid bitumen) is the same. To improve the accuracy of SEM identifications of dispersed OM in shale, correlative light and electron microscopy (CLEM) was used during this study to create optical and SEM images of OM in the same fields of view (500× magnification) under white light, blue light, secondary electron (SE), and BSE conditions. Samples ( n = 8) of varying thermal maturities and typical of the North American shale petroleum systems were used, including the Green River Mahogany Zone, Bakken Formation, Ohio Shale, Eagle Ford Formation, Barnett Formation, Haynesville Formation, and Woodford Shale. The CLEM image sets demonstrate the importance of correlative microscopy by showing how easily OM can be misidentified when viewed by SEM alone. Without CLEM techniques, petrographic data from SEM such as observations of organic nanoporosity may be misinterpreted, resulting in false or ambiguous results and impairing an improved understanding of organic diagenesis and catagenesis.
ABSTRACT Organic matter (OM) in petroleum source rocks is a mixture of organic macerals that follow their own specific evolutionary pathways during thermal maturation. Understanding the transformation of each maceral into oil and gas with increasing thermal maturity is critical for both source rock evaluation and unconventional shale oil/gas reservoir characterization. In this study, organic petrology was used to document the reflectance, abundance, color, and fluorescence properties of primary organic macerals and solid bitumen (SB) in 14 Upper Devonian New Albany Shale samples (kerogen type II sequence) from early mature (vitrinite reflectance [VR o ] of 0.55%) to post-mature (VR o 1.42%). Micro-Fourier transform infrared (micro-FTIR) spectroscopy analyses were conducted on these samples to derive information on the evolution of the chemical structure of organic macerals and SB with increasing thermal maturity. Primary OM (amorphous organic matter, alginite, vitrinite, and inertinite) and secondary organic matter (SB) were identified in early mature samples. Amorphous organic matter (AOM) was the dominant organic component in early mature samples and was observed up to the maturity equivalent to VR o 0.79% but could not be identified at VR o 0.80%. An organic network composed of AOM and SB was observed from VR o 0.55 to 0.79%, which, together with the decrease in AOM content being accompanied by an increase in SB content, suggests that with the onset of petroleum generation, SB gradually replaced the original AOM. Alginite, represented by Tasmanites cysts, started to transform to pre-oil bitumen at a maturity corresponding to VR o 0.80%. It shows weak orange-yellow fluorescence at this maturity, a change from strong greenish-yellow fluorescence in early mature samples. Alginite could not be identified at VR o 0.89%, and generated bitumen remained in place or migrated over short distances. Petrographic observations and micro-FTIR study of alginite indicate that substantial hydrocarbon generation from alginite does not start until alginite is completely transformed to pre-oil bitumen. In contrast to AOM and alginite, vitrinite and inertinite derived from terrestrial woody materials occur as dispersed particles and do not change significantly during thermal maturation. A linear relationship between vitrinite and SB reflectance exists for the studied samples. The reflectance of vitrinite is higher than that of SB until VR o 0.99%, and at higher maturities, SB reflectance exceeds vitrinite reflectance. The inclusion of pre-oil SB converted from alginite in reflectance measurements could result in a lower average SB reflectance and, therefore, caution should be applied when using SB reflectance as an indicator of thermal maturity.