322 research outputs found

    Generalized probabilities in statistical theories

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    In this review article we present different formal frameworks for the description of generalized probabilities in statistical theories. We discuss the particular cases of probabilities appearing in classical and quantum mechanics, possible generalizations of the approaches of A. N. Kolmogorov and R. T. Cox to non-commutative models, and the approach to generalized probabilities based on convex sets

    Generalizing entanglement via informational invariance for arbitrary statistical theories

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    Given an arbitrary statistical theory, different from quantum mechanics, how to decide which are the nonclassical correlations? We present a formal framework which allows for a definition of nonclassical correlations in such theories, alternative to the current one. This enables one to formulate extrapolations of some important quantum mechanical features via adequate extensions of reciprocal maps relating states of a system with states of its subsystems. These extended maps permit one to generalize i) separability measures to any arbitrary statistical model as well as ii) previous entanglement criteria. The standard definition of entanglement becomes just a particular case of the ensuing, more general notion.Comment: Improved versio

    Arbuscular mycorrhizal fungi from acidic soils favors production of tomatoes and lycopene concentration

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    This study was supported by FONDECYT 11170641 and MEC80190060 (P. Aguilera), MEC 80180077 (A. Seguel), from Agencia Nacional de Investigación y Desarrollo (ANID, Chile

    On the lattice structure of probability spaces in quantum mechanics

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    Let C be the set of all possible quantum states. We study the convex subsets of C with attention focused on the lattice theoretical structure of these convex subsets and, as a result, find a framework capable of unifying several aspects of quantum mechanics, including entanglement and Jaynes' Max-Ent principle. We also encounter links with entanglement witnesses, which leads to a new separability criteria expressed in lattice language. We also provide an extension of a separability criteria based on convex polytopes to the infinite dimensional case and show that it reveals interesting facets concerning the geometrical structure of the convex subsets. It is seen that the above mentioned framework is also capable of generalization to any statistical theory via the so-called convex operational models' approach. In particular, we show how to extend the geometrical structure underlying entanglement to any statistical model, an extension which may be useful for studying correlations in different generalizations of quantum mechanics.Comment: arXiv admin note: substantial text overlap with arXiv:1008.416

    Prospects for K+π+ννˉK^+ \to \pi^+ \nu \bar{ \nu } at CERN in NA62

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    The NA62 experiment will begin taking data in 2015. Its primary purpose is a 10% measurement of the branching ratio of the ultrarare kaon decay K+π+ννˉK^+ \to \pi^+ \nu \bar{ \nu }, using the decay in flight of kaons in an unseparated beam with momentum 75 GeV/c.The detector and analysis technique are described here.Comment: 8 pages for proceedings of 50 Years of CP

    Cardiac molecular pathways influenced by doxorubicin treatment in mice

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    Doxorubicin (DOX) is a potent chemotherapeutic with distinct cardiotoxic properties. Understanding the underlying cardiotoxic mechanisms on a molecular level would enable the early detection of cardiotoxicity and implementation of prophylactic treatment. Our goal was to map the patterns of different radiopharmaceuticals as surrogate markers of specific metabolic pathways induced by chemotherapy. Therefore, cardiac distribution of Tc-99m-sestamibi, Tc-99m-Annexin V, Tc-99m-glucaric acid and [F-18]FDG and cardiac expression of Bcl-2, caspase-3 and -8, TUNEL, HIF-1 alpha, and p53 were assessed in response to DOX exposure in mice. A total of 80 mice (64 treated, 16 controls) were evaluated. All radiopharmaceuticals showed significantly increased uptake compared to controls, with peak cardiac uptake after one (Tc-99m-Annexin V), two (Tc-99m-sestamibi), three ([F-18]FDG), or four (Tc-99m-glucaric acid) cycles of DOX. Strong correlations (p <0.01) were observed between Tc-99m-Annexin V, caspase 3 and 8, and TUNEL, and between [F-18]FDG and HIF-1 alpha. This suggests that the cardiac DOX response starts with apoptosis at low exposure levels, as indicated by Tc-99m-Annexin V and histological apoptosis markers. Late process membrane disintegration can possibly be detected by Tc-99m-sestamibi and Tc-99m-glucaric acid. [F-18]FDG signifies an early adaptive response to DOX, which can be further exploited clinically in the near future
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