Search for the decay B s 0 → η ′ K S 0
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We present a search for the decay X(3872) → π + π - π 0 in the (772 ±11) ×10 6 Y(4S)→B$\overline{B}$ data sample collected at the Belle detector, where the X(3872) is produced in B ± → K ± X(3872) and B 0 →K$^{0}_{S}$X(3872) decays. We do not observe a signal, and set 90% credible upper limits for two different models of the decay processes: if the decay products are distributed uniformly in phase space, $\mathscr{B}$(X(3872) → π + π - π 0 )<1.3%, and if M(π + π - ) is concentrated near the mass of the D 0 $\overline{D}$ 0 pair in the process X(3872) → D 0 $\overline{D}$ *0 + c.c. → D 0 $\overline{D}$ 0 π 0 → π + π - π 0 , $\mathscr{B}$(X(3872) → π + π - π 0 )<1.2×10 -3 .
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The upper bounds from the ATLAS and CMS experiments on the decay rate of the Higgs boson to two muons provide the strongest constraint on an imaginary part of the muon Yukawa coupling. This bound is more than an order of magnitude stronger than bounds from $\mathcal{CP}$-violating observables, specifically the electric dipole moment of the electron. It excludes a scenario $-$ which had been viable prior to these measurements $-$ that a complex muon Yukawa coupling is the dominant source of the baryon asymmetry. Even with this bound, the muon source can still contribute ${\cal O}(16\%)$ of the asymmetry.
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A microfluidic chip device for the purification of radiochemical compounds includes a chip having an injection channel and intersecting branch channels with a plurality of valves are located along the injection channel and branch channels and configured to retain a plug of solution containing the radiochemical compound. The chip further includes a serpentine channel segment (for separation) coupled to the output of the injection channel. A high voltage power source advances the plug of solution through the purification region and into the downstream fraction collection channel. The chip includes a downstream fraction collection channel coupled to the serpentine channel segment and having an optical and radiation detection regions. One or more branch fraction channels intersect with the fraction collection channel and include valves located therein so that the radiochemical compound that is detected using a radiation detector is directed into the desired branch fraction channel for subsequent use.
This paper reports the carbon isotopic fractionations associated with the biosynthesis of biomarker lipids in a number of cyanobacteria obtained from culture collections and isolated from the coniform mats of Yellowstone National Park. Additional information is contained in the original extended abstract.
For many fission products, the γ rays emitted following decay provide an easily-detectable signature that can be used to identify their quantities and distributions in a sample. As a result, γ-ray spectroscopy is often exploited to study fission-product yields (FPYs), provided sufficiently accurate information on the γ-ray branching ratio is available. However, in many cases, the uncertainties in the existing nuclear data are large enough that they compromise the precision achievable for modern experiments and applications. To address this need, we have developed a new experimental method that is well suited to precisely measure the γ-ray branching ratios in the decay of long-lived fission products. The approach involves the production of a radiopure sample by implantation of a mass-separated ion beam from the CAlifornium Rare Isotope Breeder Upgrade (CARIBU) facility on a thin carbon foil. The emitted β -decay radiation is detected with a 4π gas proportional counter and a meticulously efficiency-calibrated high-purity germanium (HPGe) detector. As a first measurement to demonstrate the approach, we studied the γ-ray branching ratios of the strongest transitions following the decay of ⁹⁵Zr and decay-daughter ⁹⁵Nb and determined these branching ratios to fractional precisions of 1%. We then applied this approach to determine the γ-ray branching ratios for the β decay of ¹⁴⁷Nd. The results for the γ-ray branching ratios are presented here and compared to previous results and evaluations.