257 research outputs found

    Semileptonic BcB_{c} meson decays to S-wave charmonia and X(3872)X(3872) within the covariant light-front approach

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    In this work, we investigate the semileptonic decays of BcB_{c} meson to ηc(1S,2S,3S)\eta_{c}(1S,2S,3S), ψ(1S,2S,3S)\psi(1S,2S,3S) and X(3872)X(3872) within the framework of covariant light-front quark model (CLFQM). We combine the helicity amplitudes via the corresponding form factors to obtain the branching ratios of the semileptonic decays Bc→ηc(1S,2S,3S)ℓνℓB_{c}\to \eta_{c}(1S, 2S, 3S)\ell\nu_{\ell}, Bc→ψ(1S,2S,3S))ℓνℓB_{c}\to \psi(1S, 2S, 3S))\ell\nu_{\ell} and Bc→X(3872)ℓνℓB_{c}\to X(3872)\ell\nu_{\ell} with ℓ=e,μ,τ\ell=e,\mu,\tau. In view of the RJ/ΨR_{J/\Psi} anomaly released by the LHCb collaboration, it is necessary to calculate the ratios RXR_X with X=ψ(1S,2S,3S),ηc(1S,2S,3S),X(3872)X=\psi(1S,2S,3S),\eta_c(1S,2S,3S),X(3872) systematically, which are helpful to check the lepton flavor universality (LFU). Furthermore, we also take into account another two physical observables, one is the longitudinal polarization fraction fLf_{L} and the other is the forward-backward asymmetry AFBA_{FB}, which can provide new clues to understand the RJ/ΨR_{J /\Psi} anomaly. Such theoretical predictions are necessary and interesting, which can be tested in the future LHCb experiments.Comment: 23 pages, 4 figure

    Quasi-two-body decays Bc→D∗h→DπhB_c\to D^*h\to D\pi h in the perturbative QCD

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    In this work, we investigate the quasi-two-body decays Bc→D∗h→DπhB_c\to D^*h\to D\pi h with h=(K0,π0,η,η′)h = (K^0,\pi^0,\eta,\eta^{\prime}) using the perturbative QCD(PQCD) approach. The description of final state interactions between the DπD\pi pair is achieved through the two-meson distribution amplitudes(DAs), which are normalized to the time-like form factor. The PQCD predictions on the branching ratios of the quasi-two-body decays Bc→D∗h→DπhB_c\to D^*h\to D\pi h show an obvious hierarchy: Br(Bc+→D∗+K0→D0π+K0)=(5.22−0.74+0.86)×10−6,Br(Bc+→D∗+π0→D0π+π0)=(0.93±0.26)×10−7,Br(Bc+→D∗+η→D0π+η)=(2.83−0.52+0.59)×10−8Br(B_{c}^+ \to D^{*+} K^{0}\to D^0\pi^+K^{0})=({5.22}_{-0.74}^{+0.86})\times{10}^{-6}, Br(B_{c}^+ \to D^{*+} \pi^{0}\to D^0\pi^+\pi^{0})=(0.93\pm0.26)\times{10}^{-7}, Br(B_{c}^+ \to D^{*+} \eta\to D^0\pi^+\eta) =({2.83}_{-0.52}^{+0.59})\times{10}^{-8} and Br(Bc+→D∗+η′→D0π+η′)=(1.89−0.36+0.40)×10−8Br(B_{c}^+ \to D^{*+} \eta^\prime\to D^0\pi^+\eta^\prime)=({1.89}_{-0.36}^{+0.40})\times{10}^{-8}. From the invariant mass mDπm_{D\pi}-dependence of the decay spectrum for each channel, one can find that the branching fraction is concentrated in a narrow region around the D∗D^{*} pole mass. So one can obtain the branching ratios for the corresponding two-body decays Bc→D∗+hB_c\to D^{*+}h under the narrow width approximation. We find that the branching ratios of the decays Bc→D∗+hB_c\to D^{*+}h are consistent well with the previous PQCD calculations within errors. These predictions will be tested by the future experiments.Comment: 12 pages, 3 figures, accepted for publication in Chin. Phys.

    Quasi-two-body decays Bc→K∗h→KπhB_c \to K^{*} h \to K \pi h in the perturbative QCD

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    In this work we study the quasi-two-body decays Bc→ K∗h→Kπh(h=D,Ds,K,π,η,η′)B_c \to \ K^{*} h \to K \pi h (h = D, D_s, K, \pi, \eta, \eta') in the perturbative QCD (PQCD) approach. The two-meson distribution amplitudes (DAs) ΦKπP-wave\Phi^{\text{P-wave}}_{K\pi} are introduced to describe the final state interactions of the K \pi pair, which involve the time-like form factors F_{K\pi}(s) parameterized by the relativistic Breit-Wigner function and the Gegenbauer polynomials. We calculate the branching ratios for these quasi-two-body decays, from which one can obtain the branching raios for the corresponding two-body decays under the narrow width approximation relation. We find that Bc+→K∗+D0B^+_c\to K^{*+}D^0 and Bc+→K∗0D+B^+_c\to K^{*0}D^+ have the largest branching ratios, which can reach up to 10−610^{-6}, while the branching ratios for other two-body decays are very small and only about 10−8∼10−710^{-8}\sim10^{-7}. As we expected that the branching ratios of the pure annihilation decays are usually small, while in our considered such type of decays, the channel Bc+→Kˉ∗0K+B_c^+ \to \bar K^{*0}K^{+} has the largest branching ratio, which is near 10−610^{-6}. These results are consistent with the previously PQCD calculations obtained in the two-body framework, which can be tested by the future LHCb experiments. For the decays Bc+→K∗+D0→K0π+D0,Bc+→K∗0D+→K+π−D+B_c^+ \to K^{*+} D^{0}\to K^{0}\pi^+D^{0} , B_c^+ \to K^{*0}D^{+}\to K^{+}\pi^-D^{+} and Bc+→Kˉ∗0Ds+→K−π+Ds+B_c^+ \to \bar K^{*0}D_s^{+}\to K^{-}\pi^+D_s^{+}, we calculate their direct CP violations and find that ACP(Bc+→K∗+D0→K0π+D0)=(−14.6−1.12+9.19)%A_{CP}(B_c^+ \to K^{*+}D^{0}\to K^{0}\pi^+D^{0})=(-14.6_{-1.12}^{+9.19})\% is the largest one, which is possible measured by the present LHCb experiments. For the pure annihilation type decays, there is no CP violations because only the tree operators are involved. Furthermore, we also give the differential distributions of the branching ratios and the direct CP violations for the decays Bc→K∗D(s)→KπD(s)B_c\to K^* D_{(s)}\to K \pi D_{(s)}.Comment: 15 pages, 3 figures, 2 table

    A HRNet-based Rehabilitation Monitoring System

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    The rehabilitation treatment helps to heal minor sports and occupational injuries. In a traditional rehabilitation process, a therapist will assign certain actions to a patient to perform in between hospital visits, and it will rely on the patient to remember actions correctly and the schedule to perform them. Unfortunately, many patients forget to perform actions or fail to recall actions in detail. As a consequence, the rehabilitation treatment is hampered or, in the worst case, the patient may suffer from additional injury caused by performing incorrect actions. To resolve these issues, we propose a HRNet-based rehabilitation monitoring system, which can remind a patient when to perform the actions and display the actions for the patient to follow via the patient's smartphone. In addition, it helps the therapist to monitor the progress of the rehabilitation for the patient. Our system consists of an iOS app and several components at the server side. The app is in charge of displaying and collecting action videos. The server computes the similarity score between the therapist's actions and the patient's in the videos to keep track of the number of repetitions of each action. Theses stats will be shown to both of the patient and therapist. The extensive experiments show that the F1-Score of the similarity calculation is as high as 0.9 and the soft accuracy of the number of repetitions is higher than 90%

    Raw Garlic Consumption and Risk of Liver Cancer: A Population-Based Case-Control Study in Eastern China.

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    Although the major risk factors for liver cancer have been established, preventive factors for liver cancer have not been fully explored. We evaluated the association between raw garlic consumption and liver cancer in a large population-based case-control study in Eastern China. The study was conducted in Jiangsu, China, from 2003 to 2010. A total of 2011 incident liver cancer cases and 7933 randomly selected population-controls were interviewed. Epidemiological data including raw garlic intake and other exposures were collected, and serum markers of hepatitis B virus (HBV) and hepatitis C virus (HCV) infection were assayed. Overall, eating raw garlic twice or more per week was inversely associated with liver cancer, with an adjusted odds ratio (aOR) of 0.77 (95% confidence interval (CI): 0.62-0.96) compared to those ingesting no raw garlic or less than twice per week. In stratified analyses, high intake of raw garlic was inversely associated with liver cancer among Hepatitis B surface antigen (HBsAg) negative individuals, frequent alcohol drinkers, those having history of eating mold-contaminated food or drinking raw water, and those without family history of liver cancer. Marginal interactions on an additive scale were observed between low raw garlic intake and HBsAg positivity (attributable proportion due to interaction (AP) = 0.31, 95% CI: -0.01-0.62) and heavy alcohol drinking (AP = 0.28, 95% CI: 0.00-0.57). Raw garlic consumption is inversely associated with liver cancer. Such an association shed some light on the potential etiologic role of garlic intake on liver cancer, which in turn might provide a possible dietary intervention to reduce liver cancer in Chinese population

    Validation of reference genes for gene expression studies in post-harvest leaves of tea plant (Camellia sinensis)

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    Tea is one of three major non-alcoholic beverages that are popular all around the world. The economic value of tea product largely depends on the post-harvest physiology of tea leaves. The utilization of quantitative reverse transcription polymerase chain reaction is a widely accepted and precise approach to determine the target gene expression of tea plants, and the reliability of results hinges on the selection of suitable reference genes. A few reliable reference genes have been documented using various treatments and different tissues of tea plants, but none has been done on post-harvest leaves during the tea manufacturing process. The present study selected and analyzed 15 candidate reference genes: Cs18SrRNA, CsGADPH, CsACT, CsEF-1α, CsUbi, CsTUA, Cs26SrRNA, CsRuBP, CsCYP, CselF-4α, CsMON1, CsPCS1, CsSAND, CsPPA2, CsTBP. This study made an assessment on the expression stability under two kinds of post-harvest treatment, turn over and withering, using three algorithms—GeNorm, Normfinder, and Bestkeeper. The results indicated that the three commonly used reference genes, CsTUA, Cs18SrRNA, CsRuBP, together with Cs26SrRNA, were the most unstable genes in both the turn over and withering treatments. CsACT, CsEF-1α, CsPPA2, and CsTBP were the top four reference genes in the turn over treatment, while CsTBP, CsPCS1, CsPPA2, CselF-4α, and CsACT were the five best reference genes in the withering group. The expression level of lipoxygenase genes, which were involved in a number of diverse aspects of plant physiology, including wounding, was evaluated to validate the findings. To conclude, we found a basis for the selection of reference genes for accurate transcription normalization in post-harvest leaves of tea plants
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