Supernova Observation Via Neutrino-Nucleus Elastic Scattering in the CLEAN Detector

Development of large mass detectors for low-energy neutrinos and dark matter may allow supernova detection via neutrino-nucleus elastic scattering. An elastic-scattering detector could observe a few, or more, events per ton for a galactic supernova at 10 kpc ($3.1 \times 10^{20}$ m). This large yield, a factor of at least 20 greater than that for existing light-water detectors, arises because of the very large coherent cross section and the sensitivity to all flavors of neutrinos and antineutrinos. An elastic scattering detector can provide important information on the flux and spectrum of $\nu_\mu$ and $\nu_\tau$ from supernovae. We consider many detectors and a range of target materials from $^4$He to $^{208}$Pb. Monte Carlo simulations of low-energy backgrounds are presented for the liquid-neon-based Cryogenic Low Energy Astrophysics with Noble gases (CLEAN) detector. The simulated background is much smaller than the expected signal from a galactic supernova.Comment: 10 pages, 5 figures, submitted to Phys. Rev.

Robust estimation of bacterial cell count from optical density

Optical density (OD) is widely used to estimate the density of cells in liquid culture, but cannot be compared between instruments without a standardized calibration protocol and is challenging to relate to actual cell count. We address this with an interlaboratory study comparing three simple, low-cost, and highly accessible OD calibration protocols across 244 laboratories, applied to eight strains of constitutive GFP-expressing E. coli. Based on our results, we recommend calibrating OD to estimated cell count using serial dilution of silica microspheres, which produces highly precise calibration (95.5% of residuals <1.2-fold), is easily assessed for quality control, also assesses instrument effective linear range, and can be combined with fluorescence calibration to obtain units of Molecules of Equivalent Fluorescein (MEFL) per cell, allowing direct comparison and data fusion with flow cytometry measurements: in our study, fluorescence per cell measurements showed only a 1.07-fold mean difference between plate reader and flow cytometry data