Helicity conservation and factorization-suppressed charmless B decays

Toward the goal of extracting the weak angle alpha, the decay B^0/B^0-bar to a_0^{+/-}pi^{-/+} was recently measured. The decay B^0 to a_0^+pi^- is not only forbidden in the factorization limit of the tree interaction, but also strongly suppressed for the penguin interaction if short-distance QCD dominates. This makes extraction of alpha very difficult from a^{+/-}\pi^{-/+}. We examine the simlar factorization-suppressed decays, in particular, B^0\to b_1^+pi^-. The prospect of obtaining alpha is even less promising with b_1^{+/-}pi^{-/+}. To probe how well the short-distance dominance works, we emphasize importance of testing helicity conservation in the charmless B decays with spins.Comment: The version to appear in Phys. Rev. D after minor alteration

Low-Mass Baryon-Antibaryon Enhancements in B Decays

The nature of low-mass baryon-antibaryon enhancements seen in B decays is explored. Three possibilities include (i) states near threshold as found in a model by Nambu and Jona-Lasinio, (ii) isoscalar states with $J^{PC} = 0^{\pm +}$ coupled to a pair of gluons, and (iii) low-mass enhancements favored by the fragmentation process. Ways of distinguishing these mechanisms using angular distributions and flavor symmetry are proposed.Comment: 8 pages, LaTeX, no figures, to be submitted to Phys. Rev. D. One reference adde

PO-0698: Clinical outcomes of 4D CBCT-guided stereotactic body radiotherapy for inoperable hepatocellular carcinomas

Poster: Clinical track: Gastrointestinal tumours (upper and lower GI)published_or_final_version3rd ESTRO Forum, Barcelona, Spain, 24-28 April 2015. In Radiotherapy & Oncology, 2015, v. 115, p. S342-S34

B→η(η′)K(π)B \to \eta(\eta') K(\pi) in the Standard Model with Flavor Symmetry

The observed branching ratios for $B\to K \eta'$ decays are much larger than factorization predictions in the Standard Model (SM). Many proposals have been made to reconcile the data and theoretical predictions. In this paper we study these decays within the SM using flavor U(3) symmetry. If small annihilation amplitudes are neglected, one needs 11 hadronic parameters to describe $B\to PP$ decays where $P$ can be one of the $\pi$, $K$, $\eta$ and $\eta'$ nonet mesons. We find that existing data are consistent with SM with flavor U(3) symmetry. We also predict several measurable branching ratios and CP asymmetries for $B \to K (\pi) \eta(\eta')$, $\eta(\eta')\eta(\eta')$ decays. Near future experiments can provide important tests for the Standard Model with flavor U(3) symmetry.Comment: 13 pages, 4 table

Charmless B→PPB \to PP decays using flavor SU(3) symmetry

The decays of $B$ mesons to a pair of charmless pseudoscalar ($P$) mesons are analyzed within a framework of flavor SU(3). Symmetry breaking is taken into account in tree ($T$) amplitudes through ratios of decay constants; exact SU(3) is assumed elsewhere. Acceptable fits to $B \to \pi \pi$ and $B \to K \pi$ branching ratios and CP asymmetries are obtained with tree, color-suppressed ($C$), penguin ($P$), and electroweak penguin ($P_{EW}$) amplitudes. Crucial additional terms for describing processes involving $\eta$ and $\eta'$ include a large flavor-singlet penguin amplitude ($S$) as proposed earlier and a penguin amplitude $P_{tu}$ associated with intermediate $t$ and $u$ quarks. For the $B^+ \to \pi^+ \eta'$ mode a term $S_{tu}$ associated with intermediate $t$ and $u$ quarks also may be needed. Values of the weak phase $\gamma$ are obtained consistent with an earlier analysis of $B \to VP$ decays, where $V$ denotes a vector meson, and with other analyses of CKM parameters.Comment: 26 pages, 1 figure. To be submitted to Phys. Rev. D. Reference update

Final-State Phases in B→Dπ,D∗πB \to D \pi, D^* \pi, and DρD \rho Decays

The final-state phases in $\bar{B} \to D \pi, D^* \pi$, and $D \rho$ decays appear to follow a pattern similar to those in $D \to \bar{K} \pi$, $\bar{K}^* \pi$, and $\bar{K} \rho$ decays. Each set of processes is characterized by three charge states but only two independent amplitudes, so the amplitudes form triangles in the complex plane. For the first two sets the triangles appear to have non-zero area, while for the $D \rho$ or $\bar{K} \rho$ decays the areas of the triangles are consistent with zero. Following an earlier discussion of this behavior for $D$ decays, a similar analysis is performed for B decays, and the relative phases and magnitudes of contributing amplitudes are determined. The significance of recent results on \ob \to D^{(*)0} \bar{K}^{(*)0} is noted. Open theoretical and experimental questions are indicated.Comment: 16 pages, LaTeX, 3 figures, to be submitted to Phys. Rev. D. References added; comments on new experimental results and analysi

Final-State Phases in Doubly-Cabibbo-Suppressed Charmed Meson Nonleptonic Decays

Cabibbo-favored nonleptonic charmed particle decays exhibit large final-state phase differences in $\bar K \pi$ and $\bar K^* \pi$ but not $\bar K \rho$ channels. It is of interest to know the corresponding pattern of final-state phases in doubly-Cabibbo-suppressed decays, governed by the $c \to d u \bar s$ subprocess. An experimental program is outlined for determining such phases via measurements of rates for $D \to K^* \pi$ and $K (\rho, \omega,\phi)$ channels, and determination of interference between bands in Dalitz plots. Such a program is feasible at planned high-intensity sources of charmed particles.Comment: 12 pages, LaTeX, 2 figures, to be submitted to Phys. Rev. D. Revised versio

Drosophila PQBP1 Regulates Learning Acquisition at Projection Neurons in Aversive Olfactory Conditioning

Polyglutamine tract-binding protein-1 (PQBP1) is involved in the transcription-splicing coupling, and its mutations cause a group of human mental retardation syndromes. We generated a fly model in which the Drosophila homolog of PQBP1 (dPQBP1) is repressed by insertion of piggyBac. In classical odor conditioning, learning acquisition was significantly impaired in homozygous piggyBac-inserted flies, whereas the following memory retention was completely normal. Mushroom bodies (MBs) and antennal lobes were morphologically normal in dPQBP1-mutant flies. Projection neurons (PNs) were not reduced in number and their fiber connections were not changed, whereas gene expressions including NMDA receptor subunit 1 (NR1) were decreased in PNs. Targeted double-stranded RNA-mediated silencing of dPQBP1 in PNs, but not in MBs, similarly disrupted learning acquisition. NR1 overexpression in PNs rescued the learning disturbance of dPQBP1 mutants. HDAC (histone deacetylase) inhibitors, SAHA (suberoylanilide hydroxamic acid) and PBA (phenylbutyrate), that upregulated NR1 partially rescued the learning disturbance. Collectively, these findings identify dPQBP1 as a novel gene regulating learning acquisition at PNs

Modelling of photonic wire Bragg Gratings

Some important properties of photonic wire Bragg grating structures have been investigate. The design, obtained as a generalisation of the full-width gap grating, has been modelled using 3D finite-difference time-domain simulations. Different types of stop-band have been observed. The impact of the grating geometry on the lowest order (longest wavelength) stop-band has been investigated - and has identified deeply indented configurations where reduction of the stop-bandwidth and of the reflectivity occurred. Our computational results have been substantially validated by an experimental demonstration of the fundamental stop-band of photonic wire Bragg gratings fabricated on silicon-on-insulator material. The accuracy of two distinct 2D computational models based on the effective index method has also been studied - because of their inherently much greater rapidity and consequent utility for approximate initial designs. A 2D plan-view model has been found to reproduce a large part of the essential features of the spectral response of full 3D models