Lepton Colliders at the Energy and Luminosity Frontiers: Linear Colliders and SuperB Factories

After a brief review of the performance of the various Lepton Colliders presently in operation at the energy and luminosity frontiers, the article describes their possible evolution and the envisaged new projects to improve their performances. Beauty Factories have the potential to extend the present luminosity frontier of Lepton Colliders by two orders of magnitude into the 1036 cm-2 sec-1 range. Linear Colliders have the potential to extend the present energy frontier of Lepton Colliders by one order of magnitude into the Multi-TeV energy range. The ideas and challenges to boost these frontiers in the next future are described as well as the R&D plans to demonstrate their feasibility and/or to prepare projects proposals through engineering design optimisation and industrialisation. Technically driven schedule for their possible fabrication and installation are presented

The future prospects of muon colliders and neutrino factories

The potential of muon beams for high energy physics applications is described along with the challenges of producing high quality muon beams. Two proposed approaches for delivering high intensity muon beams, a proton driver source and a positron driver source, are described and compared. The proton driver concepts are based on the studies from the Muon Accelerator Program (MAP). The MAP effort focused on a path to deliver muon-based facilities, ranging from neutrino factories to muon colliders, that could span research needs at both the intensity and energy frontiers. The Low EMittance Muon Accelerator (LEMMA) concept, which uses a positron-driven source, provides an attractive path to very high energy lepton colliders with improved particle backgrounds. The recent study of a 14 TeV muon collider in the LHC tunnel, which could leverage the existing CERN injectors and infrastructure and provide physics reach comparable to the 100 TeV FCC-hh, at lower cost and with cleaner physics conditions, is also discussed. The present status of the design and R&D efforts towards each of these sources is described. A summary of important R&D required to establish a facility path for each concept is also presented.Comment: 29 pages, 17 figure

Managing Dynamic Partial Reconfiguration on Actual Heterogeneous Platform

This paper deals with partial reconfiguration issues on heterogeneous prototyping platforms (DSP/ FPGA). An analysis of multi-standard physical layer applications in terms of reconfiguration needs permits to extract several use cases of reconfiguration in a multi-standard handset: standard switching, mode switching, bug fixing, etc. The main difference between these schemes of reconfiguration is the level of granularity of the reconfiguration. We argue that a configuration manager needs to handle this multi-granularity of reconfiguration to optimize the change of context (either reconfigurable hardware or programmable software processing components) in terms of size of code, time to reconfigure, etc. The analysis also helps to determine the accurate level of flexibility needed through the reconfigurable architecture at different scales. Within this framework partial reconfiguration is an essential feature for optimizing the reconfiguration inside FPGA. We aim indeed at providing reconfiguration adequacy between re-configurability capabilities of hardware resources and reconfiguration needs of Software Defined Radio applications. Architectural solutions are proposed to implement partial reconfiguration on existing hardware combining DSP and FPGA

Un modèle hiérarchique pour les architectures reconfigurables en radio logicielle

Cet article présente un modèle hiérarchique de la gestion de configuration d'architecture reconfigurable dédié aux systèmes multi-standards. A partir d'une étude au niveau algorithmique nous proposons de décrire un modèle fonctionnel de gestion de configuration tenant compte des besoins applicatifs. L'analyse algorithmique porte sur une chaîne d'émission multi-standards UMTS/FDD Uplink, GSM Uplink et 802.11g mode OFDM. Le but du modèle présenté est de minimiser les ressources matérielles à reconfigurer à chaque nouveau changement de contexte applicatif. Par le contrôle de la reconfiguration partielle et dynamique de la chaîne, ce modèle hiérarchique est bien adapté à la gestion des ressources hétérogènes d'un système en correspondance avec les besoins d'adaptabilité de l'application multi-standards

Staphylococcus aureus Bloodstream Infection and Endocarditis―A Prospective Cohort Study

Equipe CHU UB (EA) Pôle MERS CT3 Hors Enjeu The VIRSTA Study Group : Clinical centres: Besançon: Catherine Chirouze, Elodie Curlier, Cécile Descottes-Genon, Bruno Hoen, Isabelle Patry, Lucie Vettoretti. Dijon: Pascal Chavanet, Jean-Christophe Eicher, Sandrine Gohier-Treuvelot, Marie-Christine Greusard, Catherine Neuwirth, André Péchinot, Lionel Piroth. Lyon: Marie Célard, Catherine Cornu, François Delahaye, Malika Hadid, Pascale Rausch. Montpellier: Audrey Coma, Florence Galtier, Philippe Géraud, Hélène Jean-Pierre, Vincent Le Moing, Catherine Sportouch, Jacques Reynes. Nancy: Nejla Aissa, Thanh Doco- Lecompte, François Goehringer, Nathalie Keil, Lorraine Letranchant, Hepher Malela, Thierry May, Christine Selton-Suty. Nîmes: Nathalie Bedos, Jean-Philippe Lavigne, Catherine Lechiche, Albert Sotto. Paris: Xavier Duval, Emila Ilic Habensus, Bernard Iung, Catherine Leport, Pascale Longuet, Raymond Ruimy. Rennes: Eric Bellissant, Pierre-Yves Donnio, Fabienne Le Gac, Christian Michelet, Matthieu Revest, Pierre Tattevin, Elise Thebault. Coordination and statistical analyses: François Alla, Pierre Braquet, Marie-Line Erpelding, Laetitia Minary, Sarah Tubiana. Centre National de Référence des staphylocoques: Michèle Bès, Jérôme Etienne, Anne Tristan, François Vandenesch. Sponsor CHU de Montpellier: Sandrine Barbas, Christine Delonca, Virginie Sussmuth, Anne Verchère. Alain Makinson reviewed the manuscript for English correctness.International audienceOBJECTIVES: To update the epidemiology of S. aureus bloodstream infection (SAB) in a high-income country and its link with infective endocarditis (IE).METHODS: All consecutive adult patients with incident SAB (n = 2008) were prospectively enrolled between 2009 and 2011 in 8 university hospitals in France. RESULTS: SAB was nosocomial in 54%, non-nosocomial healthcare related in 18% and community-acquired in 26%. Methicillin resistance was present in 19% of isolates. SAB Incidence of nosocomial SAB was 0.159/1000 patients-days of hospitalization (95% confidence interval [CI] 0.111-0.219). A deep focus of infection was detected in 37%, the two most frequent were IE (11%) and pneumonia (8%). The higher rates of IE were observed in injecting drug users (IE: 38%) and patients with prosthetic (IE: 33%) or native valve disease (IE: 20%) but 40% of IE occurred in patients without heart disease nor injecting drug use. IE was more frequent in case of community-acquired (IE: 21%, adjusted odds-ratio (aOR) = 2.9, CI = 2.0-4.3) or non-nosocomial healthcare-related SAB (IE: 12%, aOR = 2.3, CI = 1.4-3.5). S. aureus meningitis (IE: 59%), persistent bacteremia at 48 hours (IE: 25%) and C-reactive protein > 190 mg/L (IE: 15%) were also independently associated with IE. Criteria for severe sepsis or septic shock were met in 30% of SAB without IE (overall in hospital mortality rate 24%) and in 51% of IE (overall in hospital mortality rate 35%).CONCLUSION: SAB is still a severe disease, mostly related to healthcare in a high-income country. IE is the most frequent complication and occurs frequently in patients without known predisposing condition

Complex nature of apparently balanced chromosomal rearrangements in patients with autism spectrum disorder

Background: Apparently balanced chromosomal rearrangements can be associated with an abnormal phenotype, including intellectual disability and autism spectrum disorder (ASD). Genome-wide microarrays reveal cryptic genomic imbalances, related or not to the breakpoints, in 25% to 50% of patients with an abnormal phenotype carrying a microscopically balanced chromosomal rearrangement. Here we performed microarray analysis of 18 patients with ASD carrying balanced chromosomal abnormalities to identify submicroscopic imbalances implicated in abnormal neurodevelopment. Methods: Eighteen patients with ASD carrying apparently balanced chromosomal abnormalities were screened using single nucleotide polymorphism (SNP) arrays. Nine rearrangements were de novo, seven inherited, and two of unknown inheritance. Genomic imbalances were confirmed by fluorescence in situ hybridization and quantitative PCR. Results: We detected clinically significant de novo copy number variants in four patients (22%), including three with de novo rearrangements and one with an inherited abnormality. The sizes ranged from 3.3 to 4.9 Mb; three were related to the breakpoint regions and one occurred elsewhere. We report a patient with a duplication of the Wolf-Hirschhorn syndrome critical region, contributing to the delineation of this rare genomic disorder. The patient has a chromosome 4p inverted duplication deletion, with a 0.5 Mb deletion of terminal 4p and a 4.2 Mb duplication of 4p16.2p16.3. The other cases included an apparently balanced de novo translocation t(5;18)(q12;p11.2) with a 4.2 Mb deletion at the 18p breakpoint, a subject with de novo pericentric inversion inv(11)(p14q23.2) in whom the array revealed a de novo 4.9 Mb deletion in 7q21.3q22.1, and a patient with a maternal inv(2)(q14.2q37.3) with a de novo 3.3 Mb terminal 2q deletion and a 4.2 Mb duplication at the proximal breakpoint. In addition, we identified a rare de novo deletion of unknown significance on a chromosome unrelated to the initial rearrangement, disrupting a single gene, RFX3. Conclusions: These findings underscore the utility of SNP arrays for investigating apparently balanced chromosomal abnormalities in subjects with ASD or related neurodevelopmental disorders in both clinical and research settings

The Case for a Muon Collider Higgs Factory

We propose the construction of a compact Muon Collider Higgs Factory. Such a machine can produce up to \sim 14,000 at 8\times 10^{31} cm^-2 sec^-1 clean Higgs events per year, enabling the most precise possible measurement of the mass, width and Higgs-Yukawa coupling constants.Comment: Supporting letter for the document: "Muon Collider Higgs Factory for Smowmass 2013", A White Paper submitted to the 2013 U.S. Community Summer Study of the Division of Particles and Fields of the American Physical Society, Y. Alexahin, et. al, FERMILAB-CONF-13-245-T (July, 2013

French Roadmap for complex Systems 2008-2009

This second issue of the French Complex Systems Roadmap is the outcome of the Entretiens de Cargese 2008, an interdisciplinary brainstorming session organized over one week in 2008, jointly by RNSC, ISC-PIF and IXXI. It capitalizes on the first roadmap and gathers contributions of more than 70 scientists from major French institutions. The aim of this roadmap is to foster the coordination of the complex systems community on focused topics and questions, as well as to present contributions and challenges in the complex systems sciences and complexity science to the public, political and industrial spheres