478 research outputs found

    Pseudo-Riemannian manifolds with recurrent spinor fields

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    The existence of a recurrent spinor field on a pseudo-Riemannian spin manifold (M,g)(M,g) is closely related to the existence of a parallel 1-dimensional complex subbundle of the spinor bundle of (M,g)(M,g). We characterize the following simply connected pseudo-Riemannian manifolds admitting such subbundles in terms of their holonomy algebras: Riemannian manifolds; Lorentzian manifolds; pseudo-Riemannian manifolds with irreducible holonomy algebras; pseudo-Riemannian manifolds of neutral signature admitting two complementary parallel isotropic distributions.Comment: 13 pages, the final versio

    How to find the holonomy algebra of a Lorentzian manifold

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    Manifolds with exceptional holonomy play an important role in string theory, supergravity and M-theory. It is explained how one can find the holonomy algebra of an arbitrary Riemannian or Lorentzian manifold. Using the de~Rham and Wu decompositions, this problem is reduced to the case of locally indecomposable manifolds. In the case of locally indecomposable Riemannian manifolds, it is known that the holonomy algebra can be found from the analysis of special geometric structures on the manifold. If the holonomy algebra g⊂so(1,n−1)\mathfrak{g}\subset\mathfrak{so}(1,n-1) of a locally indecomposable Lorentzian manifold (M,g)(M,g) of dimension nn is different from so(1,n−1)\mathfrak{so}(1,n-1), then it is contained in the similitude algebra sim(n−2)\mathfrak{sim}(n-2). There are 4 types of such holonomy algebras. Criterion how to find the type of g\mathfrak{g} are given, and special geometric structures corresponding to each type are described. To each g\mathfrak{g} there is a canonically associated subalgebra h⊂so(n−2)\mathfrak{h}\subset\mathfrak{so}(n-2). An algorithm how to find h\mathfrak{h} is provided.Comment: 15 pages; the final versio

    Visual on-line learning in distributed camera networks

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    Automatic detection of persons is an important application in visual surveillance. In general, state-of-the-art systems have two main disadvantages: First, usually a general detector has to be learned that is applicable to a wide range of scenes. Thus, the training is time-consuming and requires a huge amount of labeled data. Second, the data is usually processed centralized, which leads to a huge network traffic. Thus, the goal of this paper is to overcome these problems, which is realized by a person detection system, that is based on distributed smart cameras (DSCs). Assuming that we have a large number of cameras with partly overlapping views, the main idea is to reduce the model complexity of the detector by training a specific detector for each camera. These detectors are initialized by a pre-trained classifier, that is then adapted for a specific camera by co-training. In particular, for co-training we apply an on-line learning method (i.e., boosting for feature selection), where the information exchange is realized via mapping the overlapping views onto each other by using a homography. Thus, we have a compact scenedependent representation, which allows to train and to evaluate the classifiers on an embedded device. Moreover, since the information transfer is reduced to exchanging positions the required network-traffic is minimal. The power of the approach is demonstrated in various experiments on different publicly available data sets. In fact, we show that on-line learning and applying DSCs can benefit from each other. Index Terms — visual on-line learning, object detection, multi-camera networks 1

    Piezoelectric Silicon Micropump for Drug Delivery Applications

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    Subcutaneous injection is crucial for the treatment of many diseases. Especially for regular or continuous injections, automated dosing is beneficial. However, existing devices are large, uncomfortable, visible under clothing, or interfere with physical activity. Thus, the development of small, energy efficient and reliable patch pumps or implantable systems is necessary and research on microelectromechanical system (MEMS) based drug delivery devices has gained increasing interest. However, the requirements of medical applications are challenging and especially the dosing precision and reliability of MEMS pumps are not yet sufficiently evaluated. To enable further miniaturization, we propose a precise 5 × 5 mm2 silicon micropump. Detailed experimental evaluation of ten pumps proves a backpressure capability with air of 12.5 ± 0.8 kPa, which indicates the ability to transport bubbles. The maximal water flow rate is 74 ± 6 ”L/min and the pumps’ average blocking pressure is 51 kPa. The evaluation of the dosing precision for bolus deliveries with water and insulin shows a high repeatability of dosed package volumes. The pumps show a mean standard deviation of only 0.02 mg for 0.5 mg packages, and therefore, stay below the generally accepted 5% deviation, even for this extremely small amount. The high precision enables the combination with higher concentrated medication and is the foundation for the development of an extremely miniaturized patch pump

    Cross-Correlation of Motor Activity Signals from dc-Magnetoencephalography, Near-Infrared Spectroscopy, and Electromyography

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    Neuronal and vascular responses due to finger movements were synchronously measured using dc-magnetoencephalography (dcMEG) and time-resolved near-infrared spectroscopy (trNIRS). The finger movements were monitored with electromyography (EMG). Cortical responses related to the finger movement sequence were extracted by independent component analysis from both the dcMEG and the trNIRS data. The temporal relations between EMG rate, dcMEG, and trNIRS responses were assessed pairwise using the cross-correlation function (CCF), which does not require epoch averaging. A positive lag on a scale of seconds was found for the maximum of the CCF between dcMEG and trNIRS. A zero lag is observed for the CCF between dcMEG and EMG. Additionally this CCF exhibits oscillations at the frequency of individual finger movements. These findings show that the dcMEG with a bandwidth up to 8 Hz records both slow and faster neuronal responses, whereas the vascular response is confirmed to change on a scale of seconds

    Red Blood Cell Contamination of the Final Cell Product Impairs the Efficacy of Autologous Bone Marrow Mononuclear Cell Therapy

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    ObjectivesThe aim of this study was to identify an association between the quality and functional activity of bone marrow-derived progenitor cells (BMCs) used for cardiovascular regenerative therapies and contractile recovery in patients with acute myocardial infarction included in the placebo-controlled REPAIR-AMI (Reinfusion of Enriched Progenitor cells And Infarct Remodeling in Acute Myocardial Infarction) trial.BackgroundIsolation procedures of autologous BMCs might affect cell functionality and therapeutic efficacy.MethodsQuality of cell isolation was assessed by measuring the total number of isolated BMCs, CD34+ and CD133+ cells, their colony-forming unit (CFU) and invasion capacity, cell viability, and contamination of the final BMC preparation with thrombocytes and red blood cells (RBCs).ResultsThe number of RBCs contaminating the final cell product significantly correlated with reduced recovery of left ventricular ejection fraction 4 months after BMC therapy (p = 0.007). Higher numbers of RBCs in the BMC preparation were associated with reduced BMC viability (r = −0.23, p = 0.001), CFU capacity (r = −0.16, p = 0.03), and invasion capacity (r = −0.27, p < 0.001). To assess a causal role for RBC contamination, we coincubated isolated BMCs with RBCs for 24 h in vitro. The addition of RBCs dose-dependently abrogated migratory capacity (p = 0.003) and reduced CFU capacity (p < 0.05) of isolated BMCs. Neovascularization capacity was significantly impaired after infusion of BMCs contaminated with RBCs, compared with BMCs alone (p < 0.05). Mechanistically, the addition of RBCs was associated with a profound reduction in mitochondrial membrane potential of BMCs.ConclusionsContaminating RBCs affects the functionality of isolated BMCs and determines the extent of left ventricular ejection fraction recovery after intracoronary BMC infusion in patients with acute myocardial infarction. These results suggest a bioactivity response relationship very much like a dose–response relationship in drug trials. (Reinfusion of Enriched Progenitor cells and Infarct Remodeling in Acute Myocardial Infarction [REPAIR-AMI]; NCT00279175

    Holonomy of Einstein Lorentzian manifolds

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    The classification of all possible holonomy algebras of Einstein and vacuum Einstein Lorentzian manifolds is obtained. It is shown that each such algebra appears as the holonomy algebra of an Einstein (resp., vacuum Einstein) Lorentzian manifold, the direct constructions are given. Also the holonomy algebras of totally Ricci-isotropic Lorentzian manifolds are classified. The classification of the holonomy algebras of Lorentzian manifolds is reviewed and a complete description of the spaces of curvature tensors for these holonomies is given.Comment: Dedicated to to Mark Volfovich Losik on his 75th birthday. This version is an extended part of the previous version; another part of the previous version is extended and submitted as arXiv:1001.444

    Parallelisable Heterotic Backgrounds

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    We classify the simply-connected supersymmetric parallelisable backgrounds of heterotic supergravity. They are all given by parallelised Lie groups admitting a bi-invariant lorentzian metric. We find examples preserving 4, 8, 10, 12, 14 and 16 of the 16 supersymmetries.Comment: 17 pages, AMSLaTe

    Patenting and licensing of university research: promoting innovation or undermining academic values?

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    Since the 1980s in the US and the 1990s in Europe, patenting and licensing activities by universities have massively increased. This is strongly encouraged by governments throughout the Western world. Many regard academic patenting as essential to achieve 'knowledge transfer' from academia to industry. This trend has far-reaching consequences for access to the fruits of academic research and so the question arises whether the current policies are indeed promoting innovation or whether they are instead a symptom of a pro-intellectual property (IP) culture which is blind to adverse effects. Addressing this question requires both empirical analysis (how real is the link between academic patenting and licensing and 'development' of academic research by industry?) and normative assessment (which justifications are given for the current policies and to what extent do they threaten important academic values?). After illustrating the major rise of academic patenting and licensing in the US and Europe and commenting on the increasing trend of 'upstream' patenting and the focus on exclusive as opposed to non-exclusive licences, this paper will discuss five negative effects of these trends. Subsequently, the question as to why policymakers seem to ignore these adverse effects will be addressed. Finally, a number of proposals for improving university policies will be made
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