11,999 research outputs found

    Empirical assessment of cosmic ray propagation in magnetized molecular cloud complexes

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    Molecular clouds are complex magnetized structures, with variations over a broad range of length scales. Ionization in dense, shielded clumps and cores of molecular clouds is thought to be caused by charged cosmic rays (CRs). These CRs can also contribute to heating the gas deep within molecular clouds, and their effect can be substantial in environments where CRs are abundant. CRs propagate predominantly by diffusion in media with disordered magnetic fields. The complex magnetic structures in molecular clouds therefore determine the propagation and spatial distribution of CRs within them, and hence regulate their local ionization and heating patterns. Optical and near-infrared (NIR) polarization of starlight through molecular clouds is often used to trace magnetic fields. The coefficients of CR diffusion in magnetized molecular cloud complexes can be inferred from the observed fluctuations in these optical/NIR starlight polarisations. Here, we present calculations of the expected CR heating patterns in the star-forming filaments of IC 5146, determined from optical/NIR observations. Our calculations show that local conditions give rise to substantial variation in CR propagation. This affects the local CR heating power. Such effects are expected to be severe in star-forming galaxies rich in CRs. The molecular clouds in these galaxies could evolve differently to those in galaxies where CRs are less abundant

    A Renormalizable Supersymmetric SU(5) Model

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    In the Supersymmetric SU(5) Model of Unification with the Missing Partner Mechanism, we present a renormalizable model using the Georgi-Jarlsog mechanism to describe the fermion masses and mixing. At the meantime the proton decay rates are also suppressed to satisfy the experimental data

    Strained graphene structures: from valleytronics to pressure sensing

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    Due to its strong bonds graphene can stretch up to 25% of its original size without breaking. Furthermore, mechanical deformations lead to the generation of pseudo-magnetic fields (PMF) that can exceed 300 T. The generated PMF has opposite direction for electrons originating from different valleys. We show that valley-polarized currents can be generated by local straining of multi-terminal graphene devices. The pseudo-magnetic field created by a Gaussian-like deformation allows electrons from only one valley to transmit and a current of electrons from a single valley is generated at the opposite side of the locally strained region. Furthermore, applying a pressure difference between the two sides of a graphene membrane causes it to bend/bulge resulting in a resistance change. We find that the resistance changes linearly with pressure for bubbles of small radius while the response becomes non-linear for bubbles that stretch almost to the edges of the sample. This is explained as due to the strong interference of propagating electronic modes inside the bubble. Our calculations show that high gauge factors can be obtained in this way which makes graphene a good candidate for pressure sensing.Comment: to appear in proceedings of the NATO Advanced Research Worksho

    Systemic delivery of microRNA-101 potently inhibits hepatocellular carcinoma in vivo by repressing multiple targets

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    Targeted therapy based on adjustment of microRNA (miRNA)s activity takes great promise due to the ability of these small RNAs to modulate cellular behavior. However, the efficacy of miR-101 replacement therapy to hepatocellular carcinoma (HCC) remains unclear. In the current study, we first observed that plasma levels of miR-101 were significantly lower in distant metastatic HCC patients than in HCCs without distant metastasis, and down-regulation of plasma miR-101 predicted a worse disease-free survival (DFS, P<0.05). In an animal model of HCC, we demonstrated that systemic delivery of lentivirus-mediated miR-101 abrogated HCC growth in the liver, intrahepatic metastasis and distant metastasis to the lung and to the mediastinum, resulting in a dramatic suppression of HCC development and metastasis in mice without toxicity and extending life expectancy. Furthermore, enforced overexpression of miR-101 in HCC cells not only decreased EZH2, COX2 and STMN1, but also directly down-regulated a novel target ROCK2, inhibited Rho/Rac GTPase activation, and blocked HCC cells epithelial-mesenchymal transition (EMT) and angiogenesis, inducing a strong abrogation of HCC tumorigenesis and aggressiveness both in vitro and in vivo. These results provide proof-of-concept support for systemic delivery of lentivirus-mediated miR-101 as a powerful anti-HCC therapeutic modality by repressing multiple molecular targets. © 2015 Zheng et al.published_or_final_versio
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