Landslides and tsunamis predicted by incompressible smoothed particle hydrodynamics (SPH) with application to the 1958 Lituya Bay event and idealized experiment.

Tsunamis caused by landslides may result in significant destruction of the surroundings with both societal and industrial impact. The 1958 Lituya Bay landslide and tsunami is a recent and well-documented terrestrial landslide generating a tsunami with a run-up of 524 m. Although recent computational techniques have shown good performance in the estimation of the run-up height, they fail to capture all the physical processes, in particular, the landslide-entry profile and interaction with the water. Smoothed particle hydrodynamics (SPH) is a versatile numerical technique for describing free-surface and multi-phase flows, particularly those that exhibit highly nonlinear deformation in landslide-generated tsunamis. In the current work, the novel multi-phase incompressible SPH method with shifting is applied to the Lituya Bay tsunami and landslide and is the first methodology able to reproduce realistically both the run-up and landslide-entry as documented in a benchmark experiment. The method is the first paper to develop a realistic implementation of the physics that in addition to the non-Newtonian rheology of the landslide includes turbulence in the water phase and soil saturation. Sensitivity to the experimental initial conditions is also considered. This work demonstrates the ability of the proposed method in modelling challenging environmental multi-phase, non-Newtonian and turbulent flows.

Smoothed particle hydrodynamics method applied to pulsatile flow inside a rigid two-dimensional model of left heart cavity.

This paper aims to extend the application of smoothed particle hydrodynamics (SPH), a meshfree particle method, to simulate flow inside a model of the heart's left ventricle (LV). This work is considered the first attempt to simulate flow inside a heart cavity using a meshfree particle method. Simulating this kind of flow, characterized by high pulsatility and moderate Reynolds number using SPH is challenging. As a consequence, validation of the computational code using benchmark cases is required prior to simulating the flow inside a model of the LV. In this work, this is accomplished by simulating an unsteady oscillating flow (pressure amplitude: A = 2500 N ∕ m(3) and Womersley number: W(o) = 16) and the steady lid-driven cavity flow (Re = 3200, 5000). The results are compared against analytical solutions and reference data to assess convergence. Then, both benchmark cases are combined and a pulsatile jet in a cavity is simulated and the results are compared with the finite volume method. Here, an approach to deal with inflow and outflow boundary conditions is introduced. Finally, pulsatile inlet flow in a rigid model of the LV is simulated. The results demonstrate the ability of SPH to model complex cardiovascular flows and to track the history of fluid properties. Some interesting features of SPH are also demonstrated in this study, including the relation between particle resolution and sound speed to control compressibility effects and also order of convergence in SPH simulations, which is consistently demonstrated to be between first-order and second-order at the moderate Reynolds numbers investigated.

Inhibition of topoisomerase I function by coralyne and 5,6-dihydrocoralyne.

The antitumor agent coralyne and a number of structural analogues were found to be inhibitors of DNA topoisomerase I and were characterized biochemically. Several of these analogues stabilized the covalent binary complex formed between calf thymus topoisomerase I and pSP64 plasmid DNA; coralyne and 5,6-dihydrocoralyne had the greatest potency as inhibitors in this assay. In common with camptothecin, the effects of coralyne and 5,6-dihydrocoralyne were reversed in the presence of increasing salt concentration or temperature, consistent with the interpretation that both functioned mechanistically in a fashion analogous to camptothecin. The sequence specificity of DNA cleavage by coralyne and 5,6-dihydrocoralyne was also studied in comparison with camptothecin using a 471-bp DNA duplex as a substrate for topoisomerase I. Seven sites of cleavage were apparent, four of which were shared in common by coralyne, 5,6-dihydrocoralyne and camptothecin. Coralyne and 5,6-dihydrocoralyne produced cleavage at one sequence, 5'-TCTC decreases GTAA=3', that was not apparent in the presence of camptothecin; correspondingly, two cleavage bands appeared only when camptothecin was present. Coralyne and 5,6-dihydrocoralyne also inhibited topoisomerase I-mediated relaxation of supercoiled plasmid DNA. Coralyne was the most potent inhibitor of DNA relaxation; the effects of camptothecin and 5,6-dihydrocoralyne were roughly equal. At high concentrations, coralyne completely suppressed the formation of the topoisomerase I-DNA covalent binary complex.