Mass spectrometric study of the release of volatile fission products from irradiated LWR fuel

The objective of these studies is to experimentally determine the chemical form and the rate of release of volatile fission product species from defected irradiated LWR reactor fuel pins. After release from the defected fuel pin the gaseous species immediately enters the ionizer of a quadrupole mass spectrometer thus ensuring that their chemical form is not likely to be changed prior to identification and measurement. These studies differ from prior studies in that: (1) the chemical form of the volatile fission products will be determined; and (2) the detection and measurement method does not depend on the radioactivity of the fission product element. Information on the chemical form of the released fission product species will enable a more accurate description of their transport and reaction in the primary system. These studies are also expected to yield information on the reaction of fission products after release from the fuel oxide with the zircaloy cladding. The results of these studies are expected to increase the understanding of the first step in the release of fission products by irradiated fuel and therefore help in the accurate prediction of source terms

Improved limits on nuebar emission from mu+ decay

We investigated mu+ decays at rest produced at the ISIS beam stop target. Lepton flavor (LF) conservation has been tested by searching for \nueb via the detection reaction p(\nueb,e+)n. No \nueb signal from LF violating mu+ decays was identified. We extract upper limits of the branching ratio for the LF violating decay mu+ -> e+ \nueb \nu compared to the Standard Model (SM) mu+ -> e+ nue numub decay: BR < 0.9(1.7)x10^{-3} (90%CL) depending on the spectral distribution of \nueb characterized by the Michel parameter rho=0.75 (0.0). These results improve earlier limits by one order of magnitude and restrict extensions of the SM in which \nueb emission from mu+ decay is allowed with considerable strength. The decay \mupdeb as source for the \nueb signal observed in the LSND experiment can be excluded.Comment: 10 pages, including 1 figure, 1 tabl

Forward Beam Monitor for the KATRIN experiment

The KArlsruhe TRItium Neutrino (KATRIN) experiment aims to measure the neutrino mass with a sensitivity of 0.2 eV (90 % CL). This will be achieved by a precision measurement of the endpoint region of the β-electron spectrum of tritium decay. The β-electrons are produced in the Windowless Gaseous Tritium Source (WGTS) and guided magnetically through the beamline. In order to accurately extract the neutrino mass the source activity is required to be stable and known to a high precision. The WGTS therefore undergoes constant extensive monitoring from several measurement systems. The Forward Beam Monitor (FBM) is one such monitoring system. The FBM system comprises a complex mechanical setup capable of inserting a detector board into the KATRIN beamline with a positioning precision of better than 0.3 mm. The electron flux density at that position is on the order of 10$^6$ s$^{-1}$ mm$^{-2}$. The detector board contains two silicon detector chips of p-i-n diode type which can measure the β-electron flux from the source with a precision of 0.1 % within 60 s with an energy resolution of FWHM = 2 keV. The unique challenge in developing the FBM arises from its designated operating environment inside the Cryogenic Pumping Section which is a potentially tritium contaminated ultra-high vacuum chamber at cryogenic temperatures in the presence of a 1 T strong magnetic field. Each of these parameters do strongly limit the choice of possible materials which e.g. caused difficulties in detector noise reduction, heat dissipation and lubrication. In order to completely remove the FBM from the beam tube a 2 m long traveling distance into the beamline is needed demanding a robust as well as highly precise moving mechanism

Statistical Analysis of Different Muon-antineutrino->Electron-antineutrino Searches

A combined statistical analysis of the experimental results of the LSND and KARMEN \numubnueb oscillation search is presented. LSND has evidence for neutrino oscillations that is not confirmed by the KARMEN experiment. This joint analysis is based on the final likelihood results for both data sets. A frequentist approach is applied to deduce confidence regions. At a combined confidence level of 36%, there is no area of oscillation parameters compatible with both experiments. For the complementary confidence of 1-0.36=64%, there are two well defined regions of oscillation parameters (sin^2(2th),Dm^2) compatible with both experiments.Comment: 25 pages, including 10 figures, submitted to Phys. Rev.

The KATRIN Pre-Spectrometer at reduced Filter Energy

The KArlsruhe TRItium Neutrino experiment, KATRIN, will determine the mass of the electron neutrino with a sensitivity of 0.2 eV (90% C.L.) via a measurement of the beta-spectrum of gaseous tritium near its endpoint of E_0 =18.57 keV. An ultra-low background of about b = 10 mHz is among the requirements to reach this sensitivity. In the KATRIN main beam-line two spectrometers of MAC-E filter type are used in a tandem configuration. This setup, however, produces a Penning trap which could lead to increased background. We have performed test measurements showing that the filter energy of the pre-spectrometer can be reduced by several keV in order to diminish this trap. These measurements were analyzed with the help of a complex computer simulation, modeling multiple electron reflections both from the detector and the photoelectric electron source used in our test setup.Comment: 22 pages, 12 figure

H2.0-like Homeobox Regulates Early Hematopoiesis and Promotes Acute Myeloid Leukemia

SummaryHomeobox domain-containing transcription factors are important regulators of hematopoiesis. Here, we report that increased levels of nonclustered H2.0-like homeobox (HLX) lead to loss of functional hematopoietic stem cells and formation of aberrant progenitors with unlimited serial clonogenicity and blocked differentiation. Inhibition of HLX reduces proliferation and clonogenicity of leukemia cells, overcomes the differentiation block, and leads to prolonged survival. HLX regulates a transcriptional program, including PAK1 and BTG1, that controls cellular differentiation and proliferation. HLX is overexpressed in 87% of patients with acute myeloid leukemia (AML) and independently correlates with inferior overall survival (n = 601, p = 2.3 × 10−6). Our study identifies HLX as a key regulator in immature hematopoietic and leukemia cells and as a prognostic marker and therapeutic target in AML