Numerical analysis of deuterium migration behaviors in tungsten damaged by fast neutron by means of gas absorption method
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Successful carbon capture and storage (CCS) requires secure CO 2 confinement within a geologic reservoir. If associated with a depleted hydrocarbon reservoir, the sealing capability can be determined by examination of the shallow subsurface for hydrocarbon leaks. Numerous seismic signatures have been reported to be hydrocarbon indicators. The interpretation can be advanced by using seismic diffractions, which could indicate subtle hydrocarbon accumulations not detectable by conventional techniques. In this work, we investigate the potential of seismic diffractions for use in shallow gas detection. We extract diffractions from the ultra-high-resolution 3D P-Cable seismic dataset acquired along the Gulf of Mexico inner continental shelf. Interpretation of this dataset revealed numerous seismic signatures associated with hydrocarbon accumulations (e.g., a prominent gas chimney). We analyze scattering features of the detected hydrocarbon accumulations and confirm the correlation between confidently interpreted gas accumulations and seismic diffractions. Based on that, we suggest using diffractions for confining system integrity assessment. As a result, diffraction analysis allows operating with subtle seismic signals that facilitates exploration of reliable CO 2 storage sites.
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Purpose: To characterize the recruitment of bone marrow (BM)-derived hematopoietic stem and progenitor cells (HSPCs) within tumor microenvironment after radiation therapy (RT) in a murine, heterotopic tumor model. Methods and Materials: Lewis lung carcinoma tumors were established in C57BL/6 mice and irradiated with 30 Gy given as 2 fractions over 2 days. Tumors were imaged with positron emission tomography/computed tomography (PET/CT) and measured daily with digital calipers. The HSPC and myelomonocytic cell content was assessed via immunofluorescent staining and flow cytometry. Functionality of tumor-associated HSPCs was verified in vitro using colony-forming cell assays and in vivo by rescuing lethally irradiated C57BL/6 recipients. Results: Irradiation significantly reduced tumor volumes and tumor regrowth rates compared with nonirradiated controls. The number of CD133{sup +} HSPCs present in irradiated tumors was higher than in nonirradiated tumors during all stages of regrowth. CD11b{sup +} counts were similar. PET/CT imaging and growth rate analysis based on standardized uptake value indicated that HSPC recruitment directly correlated to the extent of regrowth and intratumor cell activity after irradiation. The BM-derived tumor-associated HSPCs successfully formed hematopoietic colonies and engrafted irradiated mice. Finally, targeted treatment with a small animal radiation research platform demonstrated localized HSPC recruitment to defined tumor subsites exposed to radiation. Conclusions: Hypofractionated irradiation resulted in a pronounced and targeted recruitment of BM-derived HSPCs, possibly as a mechanism to promote tumor regrowth. These data indicate for the first time that radiation therapy regulates HSPC content within regrowing tumors.