An Evaluation of Adaptive Partitioning of Real-Time Workloads on Linux

This paper provides an open implementation and an experimental evaluation of an adaptive partitioning approach for scheduling real-time tasks on symmetric multicore systems. The proposed technique is based on combining partitioned EDF scheduling with an adaptive migration policy that moves tasks across processors only when strictly needed to respect their temporal constraints. The implementation of the technique within the Linux kernel, via modifications to the SCHED_DEADLINE code base, is presented. An extensive experimentation-has been conducted by applying the technique on a real multi-core platform with several randomly generated synthetic task sets. The obtained experimental results highlight that the approach exhibits a promising performance to schedule real-time workloads on a real system, with a greatly reduced number of migrations compared to the original global EDF available in SCHED_DEADLINE

Bifid median nerve: report of two cases

The median nerve divides into its terminal branches at or proximal to the distal edge of the flexor retinaculum. An anatomy of the median nerve within the carpal tunnel is reported in two separate cases. Emphasis has been given to the value of direct vision when incising the flexor retinaculum in order to avoid injure of the median nerve

Performance comparison between signal digitizers and low-cost digital oscilloscopes: spectroscopic, pulse shape discrimination and timing capabilities for nuclear detectors

Signal digitizers revolutionized the approach to the electronics readout of radiation detectors in Nuclear Physics. These highly specialized pieces of equipment are designed to acquire the signals that are characteristic of the detectors in nuclear physics experiments. The functions of the several modules that were once needed for signal acquisition, can now be substituted by a single digitizer. As suggested by the name, with such readout modules, signals are first digitized (i.e. the signal waveform is sampled and converted to a digital representation) and then either stored or analyzed on-the-fly. The performances can be comparable or better than the traditional analog counterparts, in terms of energy, time resolution, and acquisition rate. In this work, we investigate the use of general-purpose digital oscilloscopes as signal digitizers for nuclear detectors. In order to have a proper comparison, we employ a distributed data acquisition system (DAQ), that standardizes the interface between the hardware and the on-line data analysis. The signals, from a set of typical radiation detectors, are digitized and analyzed with the very same algorithms in order to avoid biases due to different software analysis. We compare two traditional signal digitizers (CAEN DT5725 and CAEN DT5751) to two low-cost digital oscilloscopes (Digilent Analog Discovery 2, and Red Pitaya STEMLab 125-14), in terms of their capabilities for spectroscopy (energy resolution), time resolution, pulse shape discrimination, and maximum acquisition rate.Comment: 17 pages, 8 figures, 4 tables, Prepared for submission to JINS

Ultrasound-assisted cold pasteurization in liquid or SC-CO2

Various types of chemical and physical protocols are used, thermal treatment in particular, to increase the quality of bulk food products (for example, dates or some sort of nuts) and extend shelf life, and combinations of methods are frequently used to achieve the best results. However, the use of these processing methods is not always the best option to preserve the initial taste and appearance of food products. For instance, a product may lose its initial natural appearance and acquire different flavors due to chemical transformations that occur at certain temperatures or when the products are treated with chemicals. Non-thermal treatment methods are called “cold” pasteurization. This is a set of advanced techniques that are based on physical and chemical effects that do not result in the structural food-product transformations caused by heating. We have developed and tested a new technique for efficient food-product processing and cold pasteurization in an ultrasonic field under pressure in an atmosphere of supercritical or subcritical carbon dioxide. A laboratory-scale unit that was designed and built for this purpose has experimentally proven the feasibility of this process and demonstrated high efficiency in suppressing pathogenic flora

a distributed data acquisition system for nuclear detectors

Nowadays, many examples of data acquisition (DAQ) software for experimental nuclear physics are monolithic processes that run on a computer attached to the DAQ hardware. In this article we present a distributed DAQ system developed for the C-BORD project. With our system, we propose a novel approach, in which each task related to the different DAQ parts (acquisition, pre-process, analysis, etc.) runs in a separate process. In particular, the system is composed of a set of servers that exchange information through dedicated communication sockets. Therefore, with this architecture, an important advantage is the possibility to run the processes on different computers to distribute the computational load. The initial tests of the system have been giving excellent results, both in terms of performance (i.e., maximum acquisition rates) and stability. The project entitled "Effective container inspection at BORDer control points" (C-BORD) is funded by the European H2020 programme. Its aim is to develop a comprehensive set of technologies for the generalized non-intrusive inspection (NII) of containers and large-volume freight at the European Union border

Special nuclear material detection studies with the SMANDRA mobile system

The detection of special nuclear material has been studied with the SMANDRA mobile inspection system used both as a high sensitivity passive neutron/gamma spectroscopic tool and as an active inspection device using tagged neutrons. The detection of plutonium samples is possible with passive interrogation, the passive detection of uranium being much more difficult because of the low neutron yield and of the easiness of shielding the gamma rays. However, we show that active interrogation with tagged neutrons is able to provide signatures for the discrimination of uranium against other materials

Efficacy and Safety of Human Retinal Progenitor Cells.

PURPOSE: We assessed the long-term efficacy and safety of human retinal progenitor cells (hRPC) using established rodent models. METHODS: Efficacy of hRPC was tested initially in Royal College of Surgeons (RCS) dystrophic rats immunosuppressed with cyclosporine/dexamethasone. Due to adverse effects of dexamethasone, this drug was omitted from a subsequent dose-ranging study, where different hRPC doses were tested for their ability to preserve visual function (measured by optokinetic head tracking) and retinal structure in RCS rats at 3 to 6 months after grafting. Safety of hRPC was assessed by subretinal transplantation into wild type (WT) rats and NIH-III nude mice, with analysis at 3 to 6 and 9 months after grafting, respectively. RESULTS: The optimal dose of hRPC for preserving visual function/retinal structure in dystrophic rats was 50,000 to 100,000 cells. Human retinal progenitor cells integrated/survived in dystrophic and WT rat retina up to 6 months after grafting and expressed nestin, vimentin, GFAP, and βIII tubulin. Vision and retinal structure remained normal in WT rats injected with hRPC and there was no evidence of tumors. A comparison between dexamethasone-treated and untreated dystrophic rats at 3 months after grafting revealed an unexpected reduction in the baseline visual acuity of dexamethasone-treated animals. CONCLUSIONS: Human retinal progenitor cells appear safe and efficacious in the preclinical models used here. TRANSLATIONAL RELEVANCE: Human retinal progenitor cells could be deployed during early stages of retinal degeneration or in regions of intact retina, without adverse effects on visual function. The ability of dexamethasone to reduce baseline visual acuity in RCS dystrophic rats has important implications for the interpretation of preclinical and clinical cell transplant studies

The Effect of Hypothermic and Cryogenic Preservation on Engineered Neural Tissue

This study explored different approaches to preserve Engineered Neural Tissue (EngNT), a stabilised cellular collagen hydrogel containing columns of aligned Schwann cells for nervous system repair. The ability to preserve EngNT without disrupting cellular and extracellular components and structures is important for clinical translation and commercialisation. Stabilised cellular gels and EngNT constructs were preserved under various conditions and cell survival assessed using live/dead microscopy and metabolic assay. Optimal survival was recorded in hypothermic (4ºC) conditions for 2-3 days using Hibernate®-A media, and, for longer term cryogenic storage (liquid nitrogen), using a mixture of 60% Dulbecco's Modified Eagle's Medium media (DMEM), 30% foetal calf serum (FCS) and 10% dimethyl sulfoxide (DMSO). Functionality and structure of preserved EngNT was assessed in co-culture with dorsal root ganglion (DRG) neurons, which indicated that alignment of Schwann cells and the ability of EngNT to support and guide neuronal regeneration were not disrupted. The identification of conditions that preserve EngNT will inform development of storage and transport methodologies to support clinical and commercial translation of this technology and other therapies based on cellular hydrogels

Registration of FC1740 and FC1741 multigerm, rhizomania-resistant sugar beet germplasm with resistance to multiple diseases

FC1740 (Reg No. GP-293, PI 681717) and FC1741 (Reg No. GP-294, PI 681718) sugar beet germplasm (Beta vulgaris L.) were developed by the USDA-ARS at Fort Collins, CO, Salinas, CA, and Kimberly, ID, in cooperation with the Beet Sugar Development Foundation, Denver, CO. These germplasm are diploid, multigerm sugar beet populations in normal cytoplasm, segregating for self-sterility (Sf:SsSs), genetic male sterility (A:aa), and hypocotyl color (R:rr). FC1740 and FC1741 have excellent resistance to rhizomania (Beet necrotic yellow vein virus). FC1740 was selected as homozygous resistant to markers linked to both Rz1 and Rz2 genes for rhizomania resistance. FC1741 was selected as homozygous to the marker linked to the Rz2 gene for resistance. Both germplasm also have resistance to beet curly top (Beet curly top virus) and Fusarium yellows (Fusarium oxysporum Schlechtend.:Fr. f. sp. betae (D. Stewart) W. C. Snyder & H. N. Hans. and other Fusarium spp.), as well as moderate resistance to Aphanomyces root rot (Aphanomyces cochlioides Drechs.). Neither line exhibited resistance to Cercospora leaf spot (Cercospora beticola Sacc.), Rhizoctonia crown and root rot (Rhizoctonia solani Kuhn.) or sugar beet root aphid (Pemphigus spp.). These germplasm provide sources from which to select disease-resistant, multigerm pollinator parents with either or both of the Rz1 and Rz2 sources of rhizomania resistance. Because they are from the same population, they also are useful as controls of known genetic background in comparing entries screened for rhizomania resistance conditioned by Rz1 or Rz2