scholarly journals Optimized lepton universality tests in $$B\rightarrow V \ell {\bar{\nu }}$$ decays

2020 ◽  
Vol 80 (11) ◽  
Author(s):  
Gino Isidori ◽  
Olcyr Sumensari

AbstractWe propose improved lepton flavor universality (LFU) ratios in semileptonic $$P\rightarrow V \ell {\bar{\nu }}$$ P → V ℓ ν ¯ decays, when comparing $$\mu $$ μ and $$\tau $$ τ modes, that minimize the theoretical form-factor uncertainties. These optimized ratios are obtained with simple cuts or reweighting of the dilepton mass distributions, which imply a minimum loss of signal on the rare tauonic modes while maximizing the cancellation of theoretical uncertainties among the two modes. We illustrate the usefulness of these observables in $$B_c\rightarrow J/\psi $$ B c → J / ψ , $$B_c\rightarrow \psi (2S)$$ B c → ψ ( 2 S ) , $$B\rightarrow D^*$$ B → D ∗ and $$B_s\rightarrow D_s^*$$ B s → D s ∗ transitions, showing that in all cases we can reach $${\mathcal {O}}(1\%)$$ O ( 1 % ) uncertainties on the SM predictions of the improved LFU ratios employing conservative form-factor uncertainties.

2006 ◽  
Vol 21 (27) ◽  
pp. 5652-5659 ◽  
Author(s):  
ANTONIO PICH

Precise measurements of the τ lepton properties provide stringent tests of the Standard Model structure and accurate determinations of its parameters. We overview the present status of a few selected topics: lepton universality, QCD tests and the determination of αs, msand |Vus| from hadronic τ decays, and lepton flavor violation phenomena.


2018 ◽  
Vol 166 ◽  
pp. 00010
Author(s):  
Giancarlo D’Ambrosio

I review kaon decays. I introduce the flavor problem and possible solutions. Very rare kaon decays like [see formula in PDF] are very important to this purpose: we study also [see formula in PDF] where chiral dynamics is important to disentangle short distance effects. We have also studied lepton flavor (universality) violation in rare kaon decays and the Bardeen Buras Gerard approach to describe the [see formula in PDF] form factor.


2021 ◽  
Vol 103 (9) ◽  
Author(s):  
Stefan Groote ◽  
Mikhail A. Ivanov ◽  
Jürgen G. Körner ◽  
Valery E. Lyubovitskij ◽  
Pietro Santorelli ◽  
...  

Author(s):  
T. Geipel ◽  
W. Mader ◽  
P. Pirouz

Temperature affects both elastic and inelastic scattering of electrons in a crystal. The Debye-Waller factor, B, describes the influence of temperature on the elastic scattering of electrons, whereas the imaginary part of the (complex) atomic form factor, fc = fr + ifi, describes the influence of temperature on the inelastic scattering of electrons (i.e. absorption). In HRTEM simulations, two possible ways to include absorption are: (i) an approximate method in which absorption is described by a phenomenological constant, μ, i.e. fi; - μfr, with the real part of the atomic form factor, fr, obtained from Hartree-Fock calculations, (ii) a more accurate method in which the absorptive components, fi of the atomic form factor are explicitly calculated. In this contribution, the inclusion of both the Debye-Waller factor and absorption on HRTEM images of a (Oll)-oriented GaAs crystal are presented (using the EMS software.Fig. 1 shows the the amplitudes and phases of the dominant 111 beams as a function of the specimen thickness, t, for the cases when μ = 0 (i.e. no absorption, solid line) and μ = 0.1 (with absorption, dashed line).


2020 ◽  
Author(s):  
Nikolas Hundt

Abstract Single-molecule imaging has mostly been restricted to the use of fluorescence labelling as a contrast mechanism due to its superior ability to visualise molecules of interest on top of an overwhelming background of other molecules. Recently, interferometric scattering (iSCAT) microscopy has demonstrated the detection and imaging of single biomolecules based on light scattering without the need for fluorescent labels. Significant improvements in measurement sensitivity combined with a dependence of scattering signal on object size have led to the development of mass photometry, a technique that measures the mass of individual molecules and thereby determines mass distributions of biomolecule samples in solution. The experimental simplicity of mass photometry makes it a powerful tool to analyse biomolecular equilibria quantitatively with low sample consumption within minutes. When used for label-free imaging of reconstituted or cellular systems, the strict size-dependence of the iSCAT signal enables quantitative measurements of processes at size scales reaching from single-molecule observations during complex assembly up to mesoscopic dynamics of cellular components and extracellular protrusions. In this review, I would like to introduce the principles of this emerging imaging technology and discuss examples that show how mass-sensitive iSCAT can be used as a strong complement to other routine techniques in biochemistry.


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