289 research outputs found

    Geological and isotope-geochemical criteria of evident presence of ancient continental crust in Primorye basement

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    The totality of structural-tectonic, lithologic-mineralogical, isotope-geochemical data on the geology of Primorye and adjacent territories of Northeast China and the Amur Region allows us to justify the criterions for the existence of an ancient sialic crust in its foundation. The main of them are the following. 1. Mesozoic terrigenous rocks of the Sikhote-Alin folded formations are characterized by the Proterozoic model age, with more ancient for arkoses - to 2460 Ma (TNdDM2). They are composed mainly of granite-metamorphic mineral association and have zircons reaching the age of up to 2500 Ma. The terrigenous flysch is arkose-dominant. 2. Тhe territory of South-Western Primorye, is covered by Cenozoic basalts with Proterozoic model ages and anomalously low isotope ratios of lead [Pb206/Pb204], analogous to basalts developed on the ancient AR-PR1 lithospheric blocks. 3. Structural deformation tectonic plan reflects presence of a single ancient rigid foundation of the territory with conformly react to a change of the compression-tension regimes in long time cycles. 4. The abundance of potassium- and barium-rich magmatism with geochemical characteristics of kimberlites-lamproites very spread within Primorye and Amur Region. A similar type of magmatism is not typical for areas with juvenile crust and reflects the presence of the mature continental lithosphere. Since the late Proterozoic, the sialic crust of Primorye has been consistently degraded as a result of delamination and basification processes

    Autoresonance in a Dissipative System

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    We study the autoresonant solution of Duffing's equation in the presence of dissipation. This solution is proved to be an attracting set. We evaluate the maximal amplitude of the autoresonant solution and the time of transition from autoresonant growth of the amplitude to the mode of fast oscillations. Analytical results are illustrated by numerical simulations.Comment: 22 pages, 3 figure

    Identification of Nedd4 E3 Ubiquitin Ligase as a Binding Partner and Regulator of MAK-V Protein Kinase

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    MAK-V/Hunk is a scantily characterized AMPK-like protein kinase. Recent findings identified MAK-V as a pro-survival and anti-apoptotic protein and revealed its role in embryonic development as well as in tumorigenesis and metastasis. However molecular mechanisms of MAK-V action and regulation of its activity remain largely unknown. We identified Nedd4 as an interaction partner for MAK-V protein kinase. However, this HECT-type E3 ubiquitin ligase is not involved in the control of MAK-V degradation by the ubiquitin-proteasome system that regulates MAK-V abundance in cells. However, Nedd4 in an ubiquitin ligase-independent manner rescued developmental defects in Xenopus embryos induced by MAK-V overexpression, suggesting physiological relevance of interaction between MAK-V and Nedd4. This identifies Nedd4 as the first known regulator of MAK-V function

    The ALICE experiment at the CERN LHC

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    ALICE (A Large Ion Collider Experiment) is a general-purpose, heavy-ion detector at the CERN LHC which focuses on QCD, the strong-interaction sector of the Standard Model. It is designed to address the physics of strongly interacting matter and the quark-gluon plasma at extreme values of energy density and temperature in nucleus-nucleus collisions. Besides running with Pb ions, the physics programme includes collisions with lighter ions, lower energy running and dedicated proton-nucleus runs. ALICE will also take data with proton beams at the top LHC energy to collect reference data for the heavy-ion programme and to address several QCD topics for which ALICE is complementary to the other LHC detectors. The ALICE detector has been built by a collaboration including currently over 1000 physicists and engineers from 105 Institutes in 30 countries. Its overall dimensions are 161626 m3 with a total weight of approximately 10 000 t. The experiment consists of 18 different detector systems each with its own specific technology choice and design constraints, driven both by the physics requirements and the experimental conditions expected at LHC. The most stringent design constraint is to cope with the extreme particle multiplicity anticipated in central Pb-Pb collisions. The different subsystems were optimized to provide high-momentum resolution as well as excellent Particle Identification (PID) over a broad range in momentum, up to the highest multiplicities predicted for LHC. This will allow for comprehensive studies of hadrons, electrons, muons, and photons produced in the collision of heavy nuclei. Most detector systems are scheduled to be installed and ready for data taking by mid-2008 when the LHC is scheduled to start operation, with the exception of parts of the Photon Spectrometer (PHOS), Transition Radiation Detector (TRD) and Electro Magnetic Calorimeter (EMCal). These detectors will be completed for the high-luminosity ion run expected in 2010. This paper describes in detail the detector components as installed for the first data taking in the summer of 2008

    Centrality evolution of the charged-particle pseudorapidity density over a broad pseudorapidity range in Pb-Pb collisions at root s(NN)=2.76TeV

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    Novel noncoding antisense RNA transcribed from human anti-NOS2A locus is differentially regulated during neuronal differentiation of embryonic stem cells

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    Here, we report on the discovery of a locus in the human genome, which evolved by gene duplication followed by an internal DNA inversion. This locus exhibits high sequence similarity to the gene for the inducible isoform of NOS protein (NOS2A) and is transcribed into a noncoding RNA containing a region of significant antisense homology with the NOS2A mRNA. We show that this antisense transcript (anti-NOS2A RNA) is expressed in different types of brain tumors, including meningiomas and glioblastomas. More importantly, we demonstrate that the expression profiles of the anti-NOS2A RNA and the NOS2A mRNA exhibit concurrent reciprocal changes in undifferentiated human embryonic stem cells (hESCs) and in hESCs induced to differentiate into neurogenic precursors such as neurospheres. As NOS2A has a role in neurogenesis, our results suggest that the anti-NOS2A RNA is involved in the regulation of neuronal differentiation of hESCs through the modulation of NOS2A gene expression

    Unraveling the Mechanism of Platelet Aggregation Suppression by Monoterpenoids

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    Platelet aggregation causes various diseases and therefore challenges the development of novel antiaggregatory drugs. In this study, we report the possible mechanism of platelet aggregation suppression by newly synthesized myrtenol-derived monoterpenoids carrying different heteroatoms (sulphur, oxygen, or nitrogen). Despite all tested compounds suppressed the platelet aggregation in vitro, the most significant effect was observed for the S-containing compounds. The molecular docking confirmed the putative interaction of all tested compounds with the platelet’s P2Y12 receptor suggesting that the anti-aggregation properties of monoterpenoids are implemented by blocking the P2Y12 function. The calculated binding force depended on heteroatom in monoterpenoids and significantly decreased with the exchanging of the sulphur atom with oxygen or nitrogen. On the other hand, in NMR studies on dodecyl phosphocholine (DPC) as a membrane model, only S-containing compound was found to be bound with DPC micelles surface. Meanwhile, no stable complexes between DPC micelles with either O- or N-containing compounds were observed. The binding of S-containing compound with cellular membrane reinforces the mechanical properties of the latter, thereby preventing its destabilization and subsequent clot formation on the phospholipid surface. Taken together, our data demonstrate that S-containing myrtenol-derived monoterpenoid suppresses the platelet aggregation in vitro via both membrane stabilization and blocking the P2Y12 receptor and, thus, appears as a promising agent for hemostasis control

    Scientific program of DERICA — prospective accelerator and storage ring facility for radioactive ion beam research

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    Studies of radioactive ions (RIs) are the most thriving field of low-energy nuclear physics. In this paper, the concept and the scientific agenda of the prospective accelerator and storage ring facility for RI beam (RIB) research are proposed for a large-scale international project based at the Flerov Laboratory of Nuclear Reactions of the Joint Institute for Nuclear Research. The motivation for the new facility is discussed and its characteristics are briefly presented and shown to be comparable to those of advanced world centers, the so-called "RIB factories". In the project, the emphasis is made on studies with short-lived RIBs in storage rings. Aunique feature of the project is the possibility of studying electron-RI interactions in a collider experiment to determine the fundamental properties of nuclear matter, in particular, electromagnetic form factors of exotic nuclei
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