246 research outputs found

    EGAM Induced by Energetic-electrons and Nonlinear Interactions among EGAM, BAEs and Tearing Modes in a Toroidal Plasma

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    In this letter, it is reported that the first experimental results are associated with the GAM induced by energetic electrons (eEGAM) in HL-2A Ohmic plasma. The energetic-electrons are generated by parallel electric fields during magnetic reconnection associated with tearing mode (TM). The eEGAM localizes in the core plasma, i.e. in the vicinity of q=2 surface, and is very different from one excited by the drift-wave turbulence in the edge plasma. The analysis indicated that the eEGAM is provided with the magnetic components, whose intensities depend on the poloidal angles, and its mode numbers are jm/nj=2/0. Further, there exist intense nonlinear interactions among eEGAM, BAEs and strong tearing modes (TMs). These new findings shed light on the underlying physics mechanism for the excitation of the low frequency (LF) Alfv\'enic and acoustic uctuations.Comment: 5 pages,4 figure

    The open-charm radiative and pionic decays of molecular charmonium Y(4274)

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    In this work, we investigate the decay widths and the line shapes of the open-charm radiative and pionic decays of Y(4274) with the DsDˉs0(2317)D_s\bar{D}_{s0}(2317) molecular charmonium assignment. Our calculation indicates that the decay widths of Y(4274)→Ds+Ds∗−γY(4274)\to D^{+}_{s}D^{*-}_{s}\gamma and Y(4274)→Ds+Ds−π0Y(4274)\to D^+_{s}D^-_{s}\pi^0 can reach up to 0.05 keV and 0.75 keV, respectively. In addition, the result of the line shape of the photon spectrum of Y(4274)→Ds+Ds∗−γY(4274)\to D_s^+ {D}_s^{*-} \gamma shows that there exists a very sharp peak near the large end point of photon energy. The line shape of the pion spectrum of Y(4274)→Ds+Ds∗−π0Y(4274)\to D_s^+ {D}_s^{*-} \pi^0 is similar to that of the pion spectrum of Y(4274)→Ds+Ds∗−γY(4274)\to D_s^+ {D}_s^{*-} \gamma, where we also find a very sharp peak near the large end point of pion energy. According to our calculation, we suggest further experiments to carry out the search for the open-charm radiative and pionic decays of Y(4274).Comment: 7 pages, 6 figures, 1 table. Published versio

    Partial Wave Analysis of J/ψ→γ(K+K−π+π−)J/\psi \to \gamma (K^+K^-\pi^+\pi^-)

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    BES data on J/ψ→γ(K+K−π+π−)J/\psi \to \gamma (K^+K^-\pi^+\pi^-) are presented. The K∗Kˉ∗K^*\bar K^* contribution peaks strongly near threshold. It is fitted with a broad 0−+0^{-+} resonance with mass M=1800±100M = 1800 \pm 100 MeV, width Γ=500±200\Gamma = 500 \pm 200 MeV. A broad 2++2^{++} resonance peaking at 2020 MeV is also required with width ∼500\sim 500 MeV. There is further evidence for a 2−+2^{-+} component peaking at 2.55 GeV. The non-K∗Kˉ∗K^*\bar K^* contribution is close to phase space; it peaks at 2.6 GeV and is very different from K∗K∗ˉK^{*}\bar{K^{*}}.Comment: 15 pages, 6 figures, 1 table, Submitted to PL

    Is X(3872) {\sl Really} a Molecular State?

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    After taking into account both the pion and sigma meson exchange potential, we have performed a dynamical calculation of the D0Dˉ∗0D^0\bar{D}^{\ast0} system. The σ\sigma meson exchange potential is repulsive from heavy quark symmetry and numerically important for a loosely bound system. Our analysis disfavors the interpretation of X(3872) as a loosely bound molecular state if we use the experimental D∗DπD^\ast D\pi coupling constant g=0.59g=0.59 and a reasonable cutoff around 1 GeV, which is the typical hadronic scale. Bound state solutions with negative eigenvalues for the DDˉ∗D\bar{D}^\ast system exist only with either a very large coupling constant (two times of the experimental value) or a large cutoff (Λ∼6\Lambda \sim 6 GeV or β∼6\beta \sim 6 GeV2^2). In contrast, there probably exists a loosely bound S-wave BBˉ∗B\bar{B}^\ast molecular state. Once produced, such a molecular state would be rather stable since its dominant decay mode is the radiative decay through B∗→BγB^\ast\to B \gamma. Experimental search of these states will be very interesting.Comment: 11 pages, 7 figures, 9 tables. The version to appear in EPJ

    Study of J/Psi decays into eta Kstar Kstar-bar

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    We report the first observation of \mPJpsi \to \mPeta\mPKst\mAPKst decay in a \mPJpsi sample of 58 million events collected with the BESII detector. The branching fraction is determined to be (1.15±0.13±0.22)×10−3(1.15 \pm 0.13 \pm 0.22)\times 10^{-3}. The selected signal event sample is further used to search for the \mPY resonance through \mPJpsi \to \mPeta \mPY, \mPY\to\mPKst\mAPKst. No evidence of a signal is seen. An upper limit of \mathrm{Br}(\mPJpsi \to \mPeta \mPY)\cdot\mathrm{Br}(\mPY\to\mPKst\mAPKst) < 2.52\times 10^{-4} is set at the 90% confidence level.Comment: 11 pages, 4 figure

    Study of J\psi decaying into \omega p \bar p

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    The decay J/ψ→ωppˉJ/\psi \to \omega p \bar p is studied using a 5.8×1075.8 \times 10^7 J/ψJ/\psi event sample accumulated with the BES II detector at the Beijing electron-positron collider. The decay branching fraction is measured to be B(J/ψ→ωppˉ)=(9.8±0.3±1.4)×10−4B(J/\psi \to \omega p \bar p)=(9.8\pm 0.3\pm 1.4)\times 10^{-4}. No significant enhancement near the ppˉp\bar p mass threshold is observed, and an upper limit of B(J/ψ→ωX(1860))B(X(1860)→ppˉ)B(J/\psi \to \omega X(1860))B(X(1860)\to p\bar p) <1.5×10−5< 1.5 \times 10^{-5} is determined at the 95% confidence level, where X(1860) designates the near-threshold enhancement seen in the ppˉp\bar p mass spectrum in J/ψ→γppˉJ/\psi \to \gamma p \bar p decays.Comment: 5 pages, 4 figure

    Effects of phytosterol supplementation on growth performance, serum lipid, proinflammatory cytokines, intestinal morphology, and meat quality of white feather broilers

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    ABSTRACT: The aim of this study was to evaluate the effects of dietary phytosterol (PS) addition at different levels on growth performance, serum lipid, proinflammatory cytokines, intestinal morphology, and meat quality in broilers. A total of 600, 1-day-old male broilers were allocated into five groups with six replicates and were fed a basal diet supplemented with 0 (control group), 10, 20, 40, or 80 mg/kg PS for 42 days. Compared with the control group, the administration of PS at doses of 40 and 80 mg/kg significantly increased the average daily feed intake and average daily gain of broilers during the experimental period. Similarly, PS at a dosage of 20 and 40 mg/kg increased the concentrations of interleukin-1β, interferon-γ, interleukin-2, and interleukin-6 but decreased triglyceride, total cholesterol, and low-density lipoprotein cholesterol content of serum (P < 0.05). Dietary PS at less than or equal to 40 mg/kg level increased (P < 0.05) villus height, and villus height to crypt depth ratio in the duodenum and ileum. Supplementing PS increased the pH value at 45 min post-mortem and decreased drip loss and shear force of breast muscle (P < 0.05). Dietary PS administration at 20 and 40 mg/kg decreased malondialdehyde accumulation but increased total antioxidant capacity and superoxide dismutase activity of breast muscle compared with the control group (P < 0.05). PS increased the concentrations of total amino acids and flavor amino acids as well as eicosapentaenoic acid, docosahexaenoic acid, and total polyunsaturated fatty acids but decreased saturated fatty acids in breast muscle (P < 0.05). It was concluded that dietary PS supplementation, especially at 40 mg/kg, could improve growth performance, serum lipid, proinflammatory cytokines, intestinal morphology, and meat quality in broilers, providing insights into its application as a potential feed additive in broiler production

    Itaconic acid and dimethyl itaconate exert antibacterial activity in carbon-enriched environments through the TCA cycle

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    Itaconic acid (IA), a metabolite generated by the tricarboxylic acid (TCA) cycle in eukaryotic immune cells, and its derivative dimethyl itaconate (DI) exert antibacterial functions in intracellular environments. Previous studies suggested that IA and DI only inhibit bacterial growth in carbon-limited environments; however, whether IA and DI maintain antibacterial activity in carbon-enriched environments remains unknown. Here, IA and DI inhibited the bacteria with minimum inhibitory concentrations of 24.02 mM and 39.52 mM, respectively, in a carbon-enriched environment. The reduced bacterial pathogenicity was reflected in cell membrane integrity, motility, biofilm formation, AI-2/luxS, and virulence. Mechanistically, succinate dehydrogenase (SDH) activity and fumaric acid levels decreased in the IA and DI treatments, while isocitrate lyase (ICL) activity was upregulated. Inhibited TCA circulation was also observed through untargeted metabolomics. In addition, energy-related aspartate metabolism and lysine degradation were suppressed. In summary, these results indicated that IA and DI reduced bacterial pathogenicity while exerting antibacterial functions by inhibiting TCA circulation. This study enriches knowledge on the inhibition of bacteria by IA and DI in a carbon-mixed environment, suggesting an alternative method for treating bacterial infections by immune metabolites
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