2,556 research outputs found

    Effect of nuclear interactions of neutral kaons on CP asymmetry measurements

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    We examine the effect of the difference in nuclear interactions of K0{K}^0 and Kˉ0\bar{K}^0 mesons on the measurement of CP asymmetry for experiments at e+e−e^+e^- colliders - charm and BB-meson factories. We find that this effect on CP asymmetry can be as large as 0.3%, and therefore sufficiently significant in interpreting measurements of CP asymmetry when neutral kaons are present in the final state.Comment: accepted to PR

    Head Direction Cells and Episodic Spatial Information in Rats without a Hippocampus

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    To successfully navigate through the environment animals rely on information concerning their directional heading and location. Many cells within the postsubiculum and anterior thalamus discharge as a function of the animal’s head direction (HD), while many cells in the hippocampus discharge in relation to the animal’s location. We placed lesions in the hippocampus and recorded from HD cells in the postsubiculum and anterior thalamus. Lesions of the hippocampus did not disrupt the HD cell signal in either brain area, indicating that the HD cell signal must be generated by structures external to the hippocampus. In addition, each cell’s preferred firing direction remained stable across days when the lesioned animal was placed into a novel environment. This stability appeared to weaken after several weeks of nonexposure to the new enclosure for two out of five animals, and subsequently recorded cells from these two animals established a new angular relationship between the familiar and novel environments. Our results suggest that extra-hippocampal structures are capable of creating and maintaining a novel representation of the animal’s environmental context. This representation shares features in common with mnemonic processes involving episodic memory that until now were assumed to require an intact hippocampus

    Analysis of Modified Starch Adsorption Kinetics on Cellulose Fibers via the Modified Langmuir Adsorption Theory

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    The kinetics of starch adsorption on cellulose fibers is one of the most important criteria regarding the efficient application of papermaking additives due to the continuous nature of paper production and the concomitant need to determine optimum residence times. This study presents an analysis of the kinetics of modified starch adsorption onto cellulose fibers via the application of the modified Langmuir adsorption theory (i.e. the collision theory). A model based on this theory was used to describe the kinetics of starch binding, and to obtain the adsorption rate constant under different process conditions, which closely correspond to the conditions commonly encountered in industrial production of paper and board. The model predictions were then correlated with the experimental data. The adsorption of modified starch was found to increase by increasing the fiber consistency, shear forces (via stirring frequency) and the refining degree of fibers. The results also demonstrate that, at least in the studied range of process variables, the modified Langmuir adsorption theory can be applied to describe the adsorption kinetics of modified starch on cellulose fibers

    Light dark forces at flavor factories

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    SuperB experiment could represent an ideal environment to test a new U (1) symmetry related to light dark forces candidates. A promising discovery channel is represented by the resonant production of a boson U, followed by its decay into lepton pairs. Beyond approximations adopted in the literature, an exact tree level calculation of the radiative processes e+e−→γ,U→Ό+ÎŒâˆ’Îł,e+e−γe+ e- \rightarrow \gamma, U \rightarrow \mu^+ \mu^- \gamma, e^+ e^- \gamma and corresponding QED backgrounds is performed, including also the most important higher-order corrections. The calculation is implemented in a release of the generator BabaYaga@NLO useful for data analysis and interpretation. The distinct features of U boson production are shown and the statistical significance is analysed

    A comparative framework: how broadly applicable is a 'rigorous' critical junctures framework?

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    The paper tests Hogan and Doyle's (2007, 2008) framework for examining critical junctures. This framework sought to incorporate the concept of ideational change in understanding critical junctures. Until its development, frameworks utilized in identifying critical junctures were subjective, seeking only to identify crisis, and subsequent policy changes, arguing that one invariably led to the other, as both occurred around the same time. Hogan and Doyle (2007, 2008) hypothesized ideational change as an intermediating variable in their framework, determining if, and when, a crisis leads to radical policy change. Here we test this framework on cases similar to, but different from, those employed in developing the exemplar. This will enable us determine whether the framework's relegation of ideational change to a condition of crisis holds, or, if ideational change has more importance than is ascribed to it by this framework. This will also enable us determined if the framework itself is robust, and fit for the purposes it was designed to perform — identifying the nature of policy change

    Study of the Baryon-Antibaryon Low-Mass Enhancements in Charmless Three-body Baryonic B Decays

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    The angular distributions of the baryon-antibaryon low-mass enhancements seen in the charmless three-body baryonic B decays B+ -> p pbar K+, B0 -> p pbar Ks, and B0 -> p Lambdabar pi- are reported. A quark fragmentation interpretation is supported, while the gluonic resonance picture is disfavored. Searches for the Theta+ and Theta++ pentaquarks in the relevant decay modes and possible glueball states G with 2.2 GeV/c2 < M-ppbar < 2.4 GeV/c2 in the ppbar systems give null results. We set upper limits on the products of branching fractions, B(B0 -> Theta+ p)\times B(Theta+ -> p Ks) Theta++ pbar) \times B(Theta++ -> p K+) G K+) \times B(G -> p pbar) < 4.1 \times 10^{-7} at the 90% confidence level. The analysis is based on a 140 fb^{-1} data sample recorded on the Upsilon(4S) resonance with the Belle detector at the KEKB asymmetric-energy e+e- collider.Comment: 14 pages, 13 figure files, update of hep-ex/0409010 for journal submisssio

    Evidence for CP Violation in B0 -> D+D- Decays

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    We report measurements of the branching fraction and CP violation parameters in B0 -> D+D- decays. The results are based on a data sample that contains 535 x 10^6 BBbar pairs collected at the Upsilon(4S) resonance, with the Belle detector at the KEKB asymmetric-energy e+e- collider. We obtain [1.97 +- 0.20 (stat) +- 0.20 (syst)] x 10^(-4) for the branching fraction of B0 -> D+D-. The measured values of the CP violation parameters are: S = -1.13 +- 0.37 +- 0.09, A = 0.91 +- 0.23 +- 0.06, where the first error is statistical and the second is systematic. We find evidence of CP violation in B0 -> D+D- at the 4.1 sigma confidence level. While the value of S is consistent with expectations from other measurements, the value of the parameter A favors large direct CP violation at the 3.2 sigma confidence level, in contradiction to Standard Model expectations.Comment: 12 pages, 3 figures, submitted to PR

    No interactions between heparin and atacicept, an antagonist of B cell survival cytokines.

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    The TNF family ligands, B cell activating factor of the TNF family (BAFF, also known as B lymphocyte stimulator, BLyS) and a proliferation-inducing ligand (APRIL), share the transmembrane activator and calcium-modulator and cyclophilin ligand (CAML)-interactor (TACI) as one of their common receptors. Atacicept, a chimeric recombinant TACI/IgG1-Fc fusion protein, inhibits both ligands. TACI and APRIL also bind to proteoglycans and to heparin that is structurally related to proteoglycans. It is unknown whether the portion of TACI contained in atacicept can bind directly to proteoglycans, or indirectly via APRIL, and whether this could interfere with the anti-coagulant properties of heparin. Binding of atacicept and APRIL to proteoglycan-positive cells was measured by FACS. Activities of heparin and atacicept were measured with activated factor Xa inhibition and cell-based assays. Effects of heparin on circulating atacicept was monitored in mice. Atacicept did not bind to proteoglycan-positive cells, but when complexed to APRIL could do so indirectly via APRIL. Multimers of atacicept obtained after exposure to cysteine or BAFF 60-mer bound directly to proteoglycans. Atacicept alone, or in complex with APRIL, or in a multimeric form did not interfere with heparin activity in vitro. Conversely, heparin did not influence inhibition of BAFF and APRIL by atacicept and did not change circulating levels of atacicept. Lack of detectable interference of APRIL-bound or free atacicept on heparin activity makes it unlikely that atacicept at therapeutic doses will interfere with the function of heparin in vivo
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