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Abstract This study describes data-denial experiments conducted to examine the impact of assimilating subsets of data from the Targeted Observation by Radars and Unoccupied Aerial Systems of Supercells (TORUS) project on storm-scale ensemble forecasts of two supercells on 8 June 2019. Assimilated data from TORUS include mobile mesonet, unoccupied aerial system (UAS), and radiosonde observations. The TORUS data are divided into three spatial subsets to evaluate the importance of observing different parts of the atmosphere on forecasts of this case: the surface (SFC) subset consisting of just the near-surface mobile mesonet observations, the PBL subset consisting of UAS observations and radiosonde profiles below 762 m, and the FREE subset consisting of radiosonde profiles above 762 m. Data-denial experiments are then conducted by comparing analyses and free forecasts generated using a cycled EnKF data assimilation system assimilating conventional observations, radar observations, and all of the TORUS observations at once with experiments where one of the three subsets is removed in turn as well as a control experiment assimilating only conventional and radar observations. Our results show that assimilating all of the TORUS observations at once in the ALL experiment improves the storm-scale ensemble forecasts much more often than it degrades them and that no one subset of the TORUS data was consistently most important for improving the analyses or forecasts. 

Abstract Very different processes characterize the decoupling of neutrinos to form the cosmic neutrino background (CνB) and the much later decoupling of photons from thermal equilibrium to form the cosmic microwave background (CMB). The CνB emerges from the fuzzy, energy-dependent neutrinosphere and encodes the physics operating in the early universe in the temperature rangeT∼ 10 MeV toT∼ 10 keV. This is the epoch where beyond Standard Model (BSM) physics, especially in the neutrino sector, may be influential in setting the light element abundances, the necessarily distorted fossil neutrino energy spectra, and other light particle energy density contributions. Here we use techniques honed in extensive CMB studies to analyze the CνB as calculated in detailed neutrino energy transport and nuclear reaction simulations of the protracted weak decoupling and primordial nucleosynthesis epochs. Our moment method, relative entropy, and differential visibility approach can leverage future high precision CMB and light element primordial abundance measurements to provide new insights into the CνB and any BSM physics it encodes. We demonstrate that the evolution of the energy spectrum of the CνB throughout the weak decoupling epoch is accurately captured in the Standard Model by only three parameters per species, a non-trivial conclusion given the deviation from thermal equilibrium and the impact of the decrease of electron-positron pairs. Furthermore, we can interpret each of the three parameters as physical characteristics of a non-equilibrium system. Though the treatment presented here makes some simplifying assumptions including ignoring neutrino flavor oscillations, the success of our compact description within the Standard Model motivates its use also in BSM scenarios. We further demonstrate how observations of primordial light element abundances can be used to place constraints on the CνB energy spectrum, deriving response functions that can be applied for general deviations from a thermal spectrum. Combined with the description of those deviations that we develop here, our methods provide a convenient and powerful framework to constrain the impact of BSM physics on the CνB. 

Abstract—Accurately capturing dynamic scenes with wideranging motion and light intensity is crucial for many vision applications. However, acquiring high-speed high dynamic range (HDR) video is challenging because the camera’s frame rate restricts its dynamic range. Existing methods sacrifice speed to acquire multi-exposure frames. Yet, misaligned motion in these frames can still pose complications for HDR fusion algorithms, resulting in artifacts. Instead of frame-based exposures, we sample the videos using individual pixels at varying exposures and phase offsets. Implemented on a monochrome pixel-wise programmable image sensor, our sampling pattern captures fast motion at a high dynamic range. We then transform pixel-wise outputs into an HDR video using end-to-end learned weights from deep neural networks, achieving high spatiotemporal resolution with minimized motion blurring. We demonstrate aliasing-free HDR video acquisition at 1000 FPS, resolving fast motion under low-light conditions and against bright backgrounds — both challenging conditions for conventional cameras. By combining the versatility of pixel-wise sampling patterns with the strength of deep neural networks at decoding complex scenes, our method greatly enhances the vision system’s adaptability and performance in dynamic conditions. Index Terms—High-dynamic-range video, high-speed imaging, CMOS image sensors, programmable sensors, deep learning, convolutional neural networks. 

Abstract Cancer immunotherapy with autologous chimeric antigen receptor (CAR) T cells faces challenges in manufacturing and patient selection that could be avoided by using ‘off-the-shelf’ products, such as allogeneic CAR natural killer T (^AlloCAR-NKT) cells. Previously, we reported a system for differentiating human hematopoietic stem and progenitor cells into^AlloCAR-NKT cells, but the use of three-dimensional culture and xenogeneic feeders precluded its clinical application. Here we describe a clinically guided method to differentiate and expand IL-15-enhanced^AlloCAR-NKT cells with high yield and purity. We generated^AlloCAR-NKT cells targeting seven cancers and, in a multiple myeloma model, demonstrated their antitumor efficacy, expansion and persistence. The cells also selectively depleted immunosuppressive cells in the tumor microenviroment and antagonized tumor immune evasion via triple targeting of CAR, TCR and NK receptors. They exhibited a stable hypoimmunogenic phenotype associated with epigenetic and signaling regulation and did not induce detectable graft versus host disease or cytokine release syndrome. These properties of^AlloCAR-NKT cells support their potential for clinical translation.