Abstract — Veins recovered from deep sedimentary formations offer insights about mineral precipitates and processes that lead to sealing of underground fractures. These processes are of interest in the context of subsurface negative emissions technologies such as geologic carbon storage, where fractures are potential pathways for unwanted fluid migration. In this study, we characterized minerals and porosity of a syntaxial vein in a shale sample from the Wolfcamp formation in Texas. The original fracture has an aperture of 5 mm and is filled with distinct zones of minerals and vuggy regions. Thin-sections from cuts across the vein were examined at micron scale resolution using scanning electron microscopy, energy dispersive X-ray spectroscopy, QEMSCAN, and polarized light microscopy. Larger-scale analyses were done using synchrotron X-ray fluorescence. Collectively, these methods reveal elongated crystals of dolomite as large as 900 microns, which are overlain with a mixture of smaller crystals including calcite and ferroan dolomite. Precipitation of SiO2 is found to fill some of the void space. Mineral identification was further corroborated using powder x-ray diffraction. Quantitative analysis of a 3D image from X-ray computed tomography indicate that the vein volume contains 62% elongate dolomite crystals, 33% mixed ferroan dolomite and calcite, 1% silica, and 4% vuggy void space. Synchrotron X-ray scattering reveal that the vein mineral precipitates have porosity of ~1% and this is much less than the shale matrix porosity. The findings in this study suggest that as the formation formed and subsided, fracture fluids migrated vertically and experienced pressure changes causing exsolution of CO2. A geochemical model simulation demonstrated how this could have led to carbonate precipitation in the veins. A fundamental understanding of the sequence of vein mineral precipitation and the associated reduction in porosity may inspire strategies designed to induce fracture sealing, thus preserving the integrity of underground CO2 storage. Examples that would cause carbonate supersaturation include increasing the pH, adding divalent cations, relying on vertical migration for solution depressurization, and heating to reduce carbonate solubility.