Effect of Geological Heterogeneities on Reservoir Storage Capacity and migration of CO 2 Plume in a Deep Saline Fractured Carbonate Aquifer

In a reservoir characterization study of the Hontomín deep saline aquifer, the impact of geological heterogeneities on reservoir storage capacity and the migration of the CO2 plume is explored. This work presents, for the first time, very long-term (up to 200 years) simulations of CO2 injection into the naturally fractured Sopeña Formation, of the lower Jurassic age, at Hontomín. CO2 injection was simulated as a dual permeability case with Eclipse compositional software. The matrix permeability of the carbonate reservoir is quite low (0.5 mD) and thus fluid flow through the fractures dominates. The reservoir is dissected by eight normal faults which limited its southeast extension and divided it into several segments. The effect of geological heterogeneities was tested through scenario-based modeling and variation of parameters characterizing heterogeneity within realistic limits based on other similar formations. This modeling approach worked well in Hontomín where the database is completely scarce. The plume migration, the reservoir storage capacity, and pressure, were each influenced in diverse ways by incorporating particular types of heterogeneities. The effect of matrix heterogeneities on reservoir storage capacity was substantial (by factors up to ~2.8×), compared to the plume migration. As the reservoir matrix permeability heterogeneity increased, the reservoir storage capacity markedly decreased, whilst an increase in porosity heterogeneity significantly increased it. The vertical gas migration in the homogeneous base case was relatively larger compared to the heterogeneous cases, and gas accumulated underneath the caprock via hydrodynamic trapping. It was also observed that, in heterogeneous cases, gas saturation in rock layers from top to bottom was relatively high compared to the base case, for which most of the gas was stored in the topmost layer. In contrast, the impact on storage capacity and plume movement of matrix vertical to horizontal permeability ratio in the fractured carbonate reservoir was small. The impact of the transmissibility of faults on reservoir pressure was only observed when the CO2 plume reached their vicinity

Aberrant Mitochondrial Homeostasis in the Skeletal Muscle of Sedentary Older Adults

The role of mitochondrial dysfunction and oxidative stress has been extensively characterized in the aetiology of sarcopenia (aging-associated loss of muscle mass) and muscle wasting as a result of muscle disuse. What remains less clear is whether the decline in skeletal muscle mitochondrial oxidative capacity is purely a function of the aging process or if the sedentary lifestyle of older adult subjects has confounded previous reports. The objective of the present study was to investigate if a recreationally active lifestyle in older adults can conserve skeletal muscle strength and functionality, chronic systemic inflammation, mitochondrial biogenesis and oxidative capacity, and cellular antioxidant capacity. To that end, muscle biopsies were taken from the vastus lateralis of young and age-matched recreationally active older and sedentary older men and women (N = 10/group; ♀  =  ♂). We show that a physically active lifestyle is associated with the partial compensatory preservation of mitochondrial biogenesis, and cellular oxidative and antioxidant capacity in skeletal muscle of older adults. Conversely a sedentary lifestyle, associated with osteoarthritis-mediated physical inactivity, is associated with reduced mitochondrial function, dysregulation of cellular redox status and chronic systemic inflammation that renders the skeletal muscle intracellular environment prone to reactive oxygen species-mediated toxicity. We propose that an active lifestyle is an important determinant of quality of life and molecular progression of aging in skeletal muscle of the elderly, and is a viable therapy for attenuating and/or reversing skeletal muscle strength declines and mitochondrial abnormalities associated with aging