411 research outputs found

    Shock Breakout in 3-Dimensional Red Supergiant Envelopes

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    Using Athena++, we perform 3D Radiation-Hydrodynamic calculations of the radiative breakout of the shock wave in the outer envelope of a red supergiant (RSG) which has suffered core collapse and will become a Type IIP supernova. The intrinsically 3D structure of the fully convective RSG envelope yields key differences in the brightness and duration of the shock breakout (SBO) from that predicted in a 1D stellar model. First, the lower-density `halo' of material outside of the traditional photosphere in 3D models leads to a shock breakout at lower densities than 1D models. This would prolong the duration of the shock breakout flash at any given location on the surface to \approx1-2 hours. However, we find that the even larger impact is the intrinsically 3D effect associated with large-scale fluctuations in density that cause the shock to break out at different radii at different times. This substantially prolongs the SBO duration to \approx3-6 hours and implies a diversity of radiative temperatures, as different patches across the stellar surface are at different stages of their radiative breakout and cooling at any given time. These predicted durations are in better agreement with existing observations of SBO. The longer durations lower the predicted luminosities by a factor of 3-10 (Lbol1044erg s1L_\mathrm{bol}\sim10^{44}\mathrm{erg\ s^{-1}}), and we derive the new scalings of brightness and duration with explosion energies and stellar properties. These intrinsically 3D properties eliminate the possibility of using observed rise times to measure the stellar radius via light-travel time effects.Comment: 12 pages, 13 figures, Accepted by Ap

    Safely Learning Visuo-Tactile Feedback Policies in Real For Industrial Insertion

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    Industrial insertion tasks are often performed repetitively with parts that are subject to tight tolerances and prone to breakage. In this paper, we present a safe method to learn a visuo-tactile insertion policy that is robust against grasp pose variations while minimizing human inputs and collision between the robot and the environment. We achieve this by dividing the insertion task into two phases. In the first align phase, we learn a tactile-based grasp pose estimation model to align the insertion part with the receptacle. In the second insert phase, we learn a vision-based policy to guide the part into the receptacle. Using force-torque sensing, we also develop a safe self-supervised data collection pipeline that limits collision between the part and the surrounding environment. Physical experiments on the USB insertion task from the NIST Assembly Taskboard suggest that our approach can achieve 45/45 insertion successes on 45 different initial grasp poses, improving on two baselines: (1) a behavior cloning agent trained on 50 human insertion demonstrations (1/45) and (2) an online RL policy (TD3) trained in real (0/45)

    Modules for Experiments in Stellar Astrophysics (MESA): Convective Boundaries, Element Diffusion, and Massive Star Explosions

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    We update the capabilities of the software instrument Modules for Experiments in Stellar Astrophysics (MESA) and enhance its ease of use and availability. Our new approach to locating convective boundaries is consistent with the physics of convection, and yields reliable values of the convective core mass during both hydrogen and helium burning phases. Stars with M<8MM<8\,{\rm M_\odot} become white dwarfs and cool to the point where the electrons are degenerate and the ions are strongly coupled, a realm now available to study with MESA due to improved treatments of element diffusion, latent heat release, and blending of equations of state. Studies of the final fates of massive stars are extended in MESA by our addition of an approximate Riemann solver that captures shocks and conserves energy to high accuracy during dynamic epochs. We also introduce a 1D capability for modeling the effects of Rayleigh-Taylor instabilities that, in combination with the coupling to a public version of the STELLA radiation transfer instrument, creates new avenues for exploring Type II supernovae properties. These capabilities are exhibited with exploratory models of pair-instability supernova, pulsational pair-instability supernova, and the formation of stellar mass black holes. The applicability of MESA is now widened by the capability of importing multi-dimensional hydrodynamic models into MESA. We close by introducing software modules for handling floating point exceptions and stellar model optimization, and four new software tools -- MESAWeb, MESA-Docker, pyMESA, and mesastar.org -- to enhance MESA's education and research impact.Comment: 64 pages, 61 figures; Accepted to AAS Journal

    Reconstruction of the metabolic network of Pseudomonas aeruginosa to interrogate virulence factor synthesis

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    Virulence-linked pathways in opportunistic pathogens are putative therapeutic targets that may be associated with less potential for resistance than targets in growth-essential pathways. However, efficacy of virulence-linked targets may be affected by the contribution of virulence-related genes to metabolism. We evaluate the complex interrelationships between growth and virulence-linked pathways using a genome-scale metabolic network reconstruction of Pseudomonas aeruginosa strain PA14 and an updated, expanded reconstruction of P. aeruginosa strain PAO1. The PA14 reconstruction accounts for the activity of 112 virulence-linked genes and virulence factor synthesis pathways that produce 17 unique compounds. We integrate eight published genome-scale mutant screens to validate gene essentiality predictions in rich media, contextualize intra-screen discrepancies and evaluate virulence-linked gene distribution across essentiality datasets. Computational screening further elucidates interconnectivity between inhibition of virulence factor synthesis and growth. Successful validation of selected gene perturbations using PA14 transposon mutants demonstrates the utility of model-driven screening of therapeutic targets
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