Preliminary implementation for the new SPIRAL2 project control system

International audienceThe Spiral2 project consists of a new facility to provide high intensity rare ions beams. It is based on a primary beam driver accelerator (RFQ followed by a superconducting linac) and a rare ion production process delivering the beam either to a low energy experimental area or to the existing Ganil facility. From October this year, one ion source coupled with a first beam line section will be in test; then, the injector (ion and deuteron sources, RFQ) will be tested by the end of 2010 so the whole accelerator should be commissioned by the end of 2011; the first exotic beams being planned one year later. The accelerator control system design results from the collaboration between several institutes and Epics has been chosen as the basic framework. The paper therefore presents the main choices: MVME5500 CPUs, VME I/O boards, VxWorks, Siemens PLCs, Modbus field buses, EDM screens and Java applications, Linux PCs, use of a LabView/Epics gateway... Specific topics are the evaluation of the XAL environment, an Epics design to address the power supplies, an emittance measurement system, the development of a beam profiler interface and the investigation for a triggered acquisition system

First step towards the new SPIRAL2 project control system

International audienceThe Spiral2 project at Ganil aims to produce rare ion beams using a Uranium carbide target fission process. The accelerator consists of a RFQ followed by a superconducting cavity linac and is designed to provide high intensity primary beams (deuterons, protons or heavy ions). The accelerator should be commissioned by the end of 2011; then, the first tests aiming to produce exotic beams are planned one year later. The control system will result of the collaboration between several institutes among which the Saclay Dapnia division yet having a good experience and knowledge with Epics. So and also because of its widely used functionalities, Epics has been chosen as the basic framework for the accelerator control and people from the other laboratories belonging to the collaboration are progressively acquiring a first experience with Epics. The paper first explains the organisation of the collaboration then it describes the basic hardware and software choices for the project. Some preliminary implementations are therefore given. As the project is still in its beginning phase, the paper ends by listing some interrogations not yet solved for the control system definition and opened for discussion

On the perturbative expansion of a quantum field theory around a topological sector

The idea of treating general relativistic theories in a perturbative expansion around a topological theory has been recently put forward in the quantum gravity literature. Here we investigate the viability of this idea, by applying it to conventional Yang--Mills theory on flat spacetime. We find that the expansion around the topological theory coincides with the usual expansion around the abelian theory, though the equivalence is non-trivial. In this context, the technique appears therefore to be viable, but not to bring particularly new insights. Some implications for gravity are discussed.Comment: 7 page

Velocity-space sensitivity of the time-of-flight neutron spectrometer at JET

The velocity-space sensitivities of fast-ion diagnostics are often described by so-called weight functions. Recently, we formulated weight functions showing the velocity-space sensitivity of the often dominant beam-target part of neutron energy spectra. These weight functions for neutron emission spectrometry (NES) are independent of the particular NES diagnostic. Here we apply these NES weight functions to the time-of-flight spectrometer TOFOR at JET. By taking the instrumental response function of TOFOR into account, we calculate time-of-flight NES weight functions that enable us to directly determine the velocity-space sensitivity of a given part of a measured time-of-flight spectrum from TOFOR

Relationship of edge localized mode burst times with divertor flux loop signal phase in JET

A phase relationship is identified between sequential edge localized modes (ELMs) occurrence times in a set of H-mode tokamak plasmas to the voltage measured in full flux azimuthal loops in the divertor region. We focus on plasmas in the Joint European Torus where a steady H-mode is sustained over several seconds, during which ELMs are observed in the Be II emission at the divertor. The ELMs analysed arise from intrinsic ELMing, in that there is no deliberate intent to control the ELMing process by external means. We use ELM timings derived from the Be II signal to perform direct time domain analysis of the full flux loop VLD2 and VLD3 signals, which provide a high cadence global measurement proportional to the voltage induced by changes in poloidal magnetic flux. Specifically, we examine how the time interval between pairs of successive ELMs is linked to the time-evolving phase of the full flux loop signals. Each ELM produces a clear early pulse in the full flux loop signals, whose peak time is used to condition our analysis. The arrival time of the following ELM, relative to this pulse, is found to fall into one of two categories: (i) prompt ELMs, which are directly paced by the initial response seen in the flux loop signals; and (ii) all other ELMs, which occur after the initial response of the full flux loop signals has decayed in amplitude. The times at which ELMs in category (ii) occur, relative to the first ELM of the pair, are clustered at times when the instantaneous phase of the full flux loop signal is close to its value at the time of the first ELM

Pathogenic Germline Variants in 10,389 Adult Cancers

We conducted the largest investigation of predisposition variants in cancer to date, discovering 853 pathogenic or likely pathogenic variants in 8% of 10,389 cases from 33 cancer types. Twenty-one genes showed single or cross-cancer associations, including novel associations of SDHA in melanoma and PALB2 in stomach adenocarcinoma. The 659 predisposition variants and 18 additional large deletions in tumor suppressors, including ATM, BRCA1, and NF1, showed low gene expression and frequent (43%) loss of heterozygosity or biallelic two-hit events. We also discovered 33 such variants in oncogenes, including missenses in MET, RET, and PTPN11 associated with high gene expression. We nominated 47 additional predisposition variants from prioritized VUSs supported by multiple evidences involving case-control frequency, loss of heterozygosity, expression effect, and co-localization with mutations and modified residues. Our integrative approach links rare predisposition variants to functional consequences, informing future guidelines of variant classification and germline genetic testing in cancer. A pan-cancer analysis identifies hundreds of predisposing germline variants

Molecular basis of haemoglobinopathies and G6PD deficiency in the Comorian population

INTRODUCTION: The Comoro archipelago is characterised by a high prevalence of red cell genetic disorders such as G6PD deficiency and haemoglobinopathies, being a region endemic for malaria. Over the last 15 years, the city of Marseilles in France has become the main destination for Comorian immigrants. This Comorian community includes patients with sickle cell disease, sickle cell/beta-thalassaemia trait, thalassaemias and G6PD deficiency. MATERIALS AND METHODS: Allele frequencies for haemoglobin S, beta-thalassaemia and G6PD deficiency were determined from neonatal and prenatal screenings of the Comorian community. Haemoglobin fractions were detected by isoelectrofocalisation, and the quantitation of HbS, HbA, HbA(2) and HbF was performed by cation exchange high performance liquid chromatography. The molecular study involved 31 alleles carrying the betaS mutation (Cd 6 [A-->T]), six beta-thalassaemic alleles and 17 G6PD-deficient alleles, selected from a group of carriers or affected subjects. RESULTS: Allele frequencies were 3% for haemoglobin S, 1% for beta-thalassaemia trait and 9.5% for G6PD deficiency. Molecular analysis had revealed that the African alleles are predominant, being present in almost all the subjects studied. Mediterranean alleles were found for all the beta-thalassaemia mutations and for three G6PD chromosomes out of 17. CONCLUSION: These data are consistent with the mixed Arab and African origin of the population of the Comoro Islands, and are of clinical interest in prenatal and newborn screening plan

Stratégie de miniaturisation d'une antenne fil-plaque monopolaire chargée par des matériaux magnéto-diélectriques

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