9 research outputs found

    Regional Heat Flow Analysis Reveals Frictionally Weak Dead Sea Fault

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    Abstract The strength of faults was vigorously debated for years, but lately a growing number of studies suggest that faults are weaker than originally suggested. Nonetheless, only a handful of natural faults have been studied in detail, and only one, the San Andreas, is a strike‐slip fault. Here, we reanalyze 268 surface heat flow measurements taken in the proximity of the southern Dead Sea Transform fault to evaluate its friction. To account for large terrain relief, and the presence of salt diapirs, we apply 3‐D terrain and salt diapir corrections. Based on these corrected heat flow values we estimate that the long‐term frictional resistance of the Dead Sea fault is 0.28 ± 0.17. This low value is similar to friction estimates from the San Andreas fault and several subduction zones

    Megathrust locking encoded in subduction landscapes

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    International audienceLocked areas of subduction megathrusts are increasingly found to coincide with landscape features sculpted over hundreds of thousand years, yet the mechanisms that underlie such correlations remain elusive. We show that interseismic locking gradients induce increments of irreversible strain across the overriding plate manifested predominantly as distributed seismicity. Summing these increments over hundreds of earthquake cycles produces a spatially variable field of uplift representing the unbalance of co-, post-, and interseismic strain. This long-term uplift explains first-order geomorphological features of subduction zones such as the position of the continental erosive shelf break, the distribution of marine terraces and peninsulas, and the profile of forearc rivers. Inelastic yielding of the forearc thus encodes short-term locking patterns in subduction landscapes, hinting that megathrust locking is stable over multiple earthquake cycles and highlighting the role geomorphology can play in constraining Earth’s greatest source of seismic hazard

    Anti-Cancer Effects of Cyclic Peptide ALOS4 in a Human Melanoma Mouse Model

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    We examined the effects of ALOS4, a cyclic peptide discovered previously by phage library selection against integrin αvÎČ3, on a human melanoma (A375) xenograft model to determine its abilities as a potential anti-cancer agent. We found that ALOS4 promoted healthy weight gain in A375-engrafted nude mice and reduced melanoma tumor mass and volume. Despite these positive changes, examination of the tumor tissue did not indicate any significant effects on proliferation, mitotic index, tissue vascularization, or reduction of αSMA or Ki-67 tumor markers. Modulation in overall expression of critical downstream αvÎČ3 integrin factors, such as FAK and Src, as well as reductions in gene expression of c-Fos and c-Jun transcription factors, indirectly confirmed our suspicions that ALOS4 is likely acting through an integrin-mediated pathway. Further, we found no overt formulation issues with ALOS4 regarding interaction with standard inert laboratory materials (polypropylene, borosilicate glass) or with pH and temperature stability under prolonged storage. Collectively, ALOS4 appears to be safe, chemically stable, and produces anti-cancer effects in a human xenograft model of melanoma. We believe these results suggest a role for ALOS4 in an integrin-mediated pathway in exerting its anti-cancer effects possibly through immune response modulation
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