320 research outputs found

    Localizable Entanglement

    Get PDF
    We consider systems of interacting spins and study the entanglement that can be localized, on average, between two separated spins by performing local measurements on the remaining spins. This concept of Localizable Entanglement (LE) leads naturally to notions like entanglement length and entanglement fluctuations. For both spin-1/2 and spin-1 systems we prove that the LE of a pure quantum state can be lower bounded by connected correlation functions. We further propose a scheme, based on matrix-product states and the Monte Carlo method, to efficiently calculate the LE for quantum states of a large number of spins. The virtues of LE are illustrated for various spin models. In particular, characteristic features of a quantum phase transition such as a diverging entanglement length can be observed. We also give examples for pure quantum states exhibiting a diverging entanglement length but finite correlation length. We have numerical evidence that the ground state of the antiferromagnetic spin-1 Heisenberg chain can serve as a perfect quantum channel. Furthermore, we apply the numerical method to mixed states and study the entanglement as a function of temperature.Comment: 19 pages, modified definition of connected string order parameter, updated reference

    Tripartite to Bipartite Entanglement Transformations and Polynomial Identity Testing

    Full text link
    We consider the problem of deciding if a given three-party entangled pure state can be converted, with a non-zero success probability, into a given two-party pure state through local quantum operations and classical communication. We show that this question is equivalent to the well-known computational problem of deciding if a multivariate polynomial is identically zero. Efficient randomized algorithms developed to study the latter can thus be applied to the question of tripartite to bipartite entanglement transformations

    Imaging Neurodegenerative Metabolism in Amyotrophic Lateral Sclerosis with Hyperpolarized [1-13C]pyruvate MRI

    Get PDF
    The cause of amyotrophic lateral sclerosis (ALS) is still unknown, and consequently, early diagnosis of the disease can be difficult and effective treatment is lacking. The pathology of ALS seems to involve specific disturbances in carbohydrate metabolism, which may be diagnostic and therapeutic targets. Magnetic resonance imaging (MRI) with hyperpolarized [1-(13)C]pyruvate is emerging as a technology for the evaluation of pathway-specific changes in the brain’s metabolism. By imaging pyruvate and the lactate and bicarbonate it is metabolized into, the technology is sensitive to the metabolic changes of inflammation and mitochondrial dysfunction. In this study, we performed hyperpolarized MRI of a patient with newly diagnosed ALS. We found a lateralized difference in [1-(13)C]pyruvate-to-[1-(13)C]lactate exchange with no changes in exchange from [1-(13)C]pyruvate to (13)C-bicarbonate. The 40% increase in [1-(13)C]pyruvate-to-[1-(13)C]lactate exchange corresponded with the patient’s symptoms and presentation with upper-motor neuron affection and cortical hyperexcitability. The data presented here demonstrate the feasibility of performing hyperpolarized MRI in ALS. They indicate potential in pathway-specific imaging of dysfunctional carbohydrate metabolism in ALS, an enigmatic neurodegenerative disease

    On Random Unitary Channels

    Full text link
    In this article we provide necessary and sufficient conditions for a completely positive trace-preserving (CPT) map to be decomposable into a convex combination of unitary maps. Additionally, we set out to define a proper distance measure between a given CPT map and the set of random unitary maps, and methods for calculating it. In this way one could determine whether non-classical error mechanisms such as spontaneous decay or photon loss dominate over classical uncertainties, for example in a phase parameter. The present paper is a step towards achieving this goal.Comment: 11 pages, typeset using RevTeX

    SBF Distances to Dwarf Elliptical Galaxies in the Sculptor Group

    Get PDF
    As part of an ongoing search for dwarf elliptical galaxies (dE) in the vicinity of the Local Group, we acquired deep B and R-band images for five dE candidates identified in the Sculptor (Scl) group region. We carried out a surface brightness fluctuation (SBF) analysis on the R-band images to measure the apparent fluctuation magnitude \bar{m}_R for each dE. Using predictions from stellar population synthesis models the galaxy distances were determined. All of these dE candidates turned out to be satellites of Scl group major members. A redshift measurement of the dE candidate ESO294-010 yielded an independent confirmation of its group membership: the [OIII] and Hα_\alpha emission lines from a small HII region gave a heliocentric velocity of 117(\pm 5) km s-1, in close agreement with the velocity of its parent galaxy NGC 55 (v_\odot=125 km s-1). The precision of the SBF distances (5 to 10%) contributes to delineating the cigar-like distribution of the Scl group members, which extend over distances from 1.7 to 4.4 Mpc and are concentrated in three, possibly four subclumps. The Hubble diagram for nine Scl galaxies, including two of our dEs, exhibits a tight linear velocity--distance relation with a steep slope of 119 km s-1 Mpc-1. The results indicate that gravitational interaction among the Scl group members plays only a minor role in the dynamics of the group. However, the Hubble flow of the entire system appears strongly disturbed by the large masses of our Galaxy and M31 leading to the observed shearing motion. From the distances and velocities of 49 galaxies located in the Local Group and towards the Scl group, we illustrate the continuity of the galaxy distribution which strongly supports the view that the two groups form a single supergalactic structure.Comment: To appear in The Astronomical Journal, December 1998; 28 pages with 22 figure

    Biosynthetic Oligoclonal Antivenom (BOA) for Snakebite and Next-Generation Treatments for Snakebite Victims

    Get PDF
    Snakebite envenoming is a neglected tropical disease that each year claims the lives of 80,000⁻140,000 victims worldwide. The only effective treatment against envenoming involves intravenous administration of antivenoms that comprise antibodies that have been isolated from the plasma of immunized animals, typically horses. The drawbacks of such conventional horse-derived antivenoms include their propensity for causing allergenic adverse reactions due to their heterologous and foreign nature, an inability to effectively neutralize toxins in distal tissue, a low content of toxin-neutralizing antibodies, and a complex manufacturing process that is dependent on husbandry and procurement of snake venoms. In recent years, an opportunity to develop a fundamentally novel type of antivenom has presented itself. By using modern antibody discovery strategies, such as phage display selection, and repurposing small molecule enzyme inhibitors, next-generation antivenoms that obviate the drawbacks of existing plasma-derived antivenoms could be developed. This article describes the conceptualization of a novel therapeutic development strategy for biosynthetic oligoclonal antivenom (BOA) for snakebites based on recombinantly expressed oligoclonal mixtures of human monoclonal antibodies, possibly combined with repurposed small molecule enzyme inhibitors
    corecore