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The gyromagnetic factor of the low-lying E=251.96(9) keV isomeric state of the nucleus ^{99}Zr was measured using the time-dependent perturbed angular distribution technique. This level is assigned a spin and parity of J^{π}=7/2^{+}, with a half-life of T_{1/2}=336(5) ns. The isomer was produced and spin aligned via the abrasion-fission of a ^{238}U primary beam at RIKEN RIBF. A magnetic moment |μ|=2.31(14)μ_{N} was deduced showing that this isomer is not single particle in nature. A comparison of the experimental values with interacting boson-fermion model IBFM-1 results shows that this state is strongly mixed with a main νd_{5/2} composition. Furthermore, it was found that monopole single-particle evolution changes significantly with the appearance of collective modes, likely due to type-II shell evolution.

We report on the operation of co-located ${}^{129}$Xe and ${}^{131}$Xe nuclear spin masers with an external feedback scheme, and discuss the use of ${}^{131}$Xe as a comagnetometer in measurements of the ${}^{129}$Xe spin precession frequency. By applying a correction based on the observed change in the ${}^{131}$Xe frequency, the frequency instability due to magnetic field and cell temperature drifts are eliminated by two orders of magnitude. The frequency precision of 6.2 $\mu$Hz is obtained for a 10$^4$ s averaging time, suggesting the possibility of future improvement to $\approx$ 1 nHz by improving the signal-to-noise ratio of the observation., Comment: 8 pages, 5 figures

Exotic nuclei are characterized by a number of neutrons (or protons) in excess relative to stable nuclei. Their shell structure, which represents single-particle motion in a nucleus, may vary due to nuclear force and excess neutrons, in a phenomenon called shell evolution. This effect could be counterbalanced by collective modes causing deformations of the nuclear surface. Here, we study the interplay between shell evolution and shape deformation by focusing on the magnetic moment of an isomeric state of the neutron-rich nucleus 75Cu. We measure the magnetic moment using highly spin-controlled rare-isotope beams and achieving large spin alignment via a two-step reaction scheme that incorporates an angular-momentum-selecting nucleon removal. By combining our experiments with numerical simulations of many-fermion correlations, we find that the low-lying states in 75Cu are, to a large extent, of single-particle nature on top of a correlated 74Ni core. We elucidate the crucial role of shell evolution even in the presence of the collective mode, and within the same framework, we consider whether and how the double magicity of the 78Ni nucleus is restored, which is also of keen interest from the perspective of nucleosynthesis in explosive stellar processes., 10 pages, 4 figures

We demonstrate spin-exchange optical pumping of 129Xe atoms with our newly made laser system. The new laser system was prepared to provide higher laser power required for the stable operation of spin maser oscillations in the 129Xe EDM experiment. We studied the optimum cell temperature and pumping laser power to improve the degree of 129Xe spin polarization. The best performance was achieved at the cell temperature of 100 ◦C with the presently available laser power of 1 W. The results show that a more intense laser is required for further improvement of the spin polarization at higher cell temperatures in our experiment.

We search for 129Xe EDM by using an active nuclear spin maser. In this experiment, the amplitude of the maser oscillation signal is one of the most important parameters that eventually determine the frequency precision. The amplitude is proportional to the ratio of the transverse spin relaxation time T 2 to the effective longitudinal spin relaxation time $T_{1}^{\ast }$ . In particular, for a spin maser of 3He (a co-magnetometer) for which $T_{1}^{\ast }$ typically reaches ∼50 h, a long T 2 is needed. T 2 depends on the homogeneity of the magnetic field which is applied with coils in order to keep the spins under precession. In the present report, we discuss on the design and construction of a new coil which provided a root-mean square (rms) field gradient of less than 5.0 μG/cm. The result of the field measurement has shown that the field gradient in the cell fulfills the target condition $\sqrt {\langle {(\nabla B_{z})^{2}} \rangle }

Co-magnetometry enables the elimination of systematic errors arising from the long-term drift in the magnetic field, and is essential for a precision measurement of spin precession frequency in experiments searching for electric dipole moment (EDM). $^{131}$Xe nuclear spin maser shows great promise as a co-magnetometer in a Xe EDM experiment, because the systematic error originating from the Xe-Rb interaction, which virtually limits the sensitivity in a case of a $^3$He co-magnetometer, will be cancelled out. The performance of a cell which contains both $^{129}$Xe and $^{131}$Xe was investigated. In the best cell among those fabricated this time, the signal-to-noise ratio in a free induction decay experiment turned out to be large enough for the operation as co-existing $^{129}$Xe-$^{131}$Xe masers.

Traditional “magic numbers” were once regarded as immutable throughout the nuclear chart. However, unexpected changes were found for unstable nuclei around N = 20. With both proton and neutron numbers around the magic number of 20, the neutron-rich 39Cl isotope provides a good test case for the study of the quantum-state evolution across the major shell. In the present work, the negative parity states in 39Cl are investigated through the β decay spectroscopy of 39S. Newly observed γ transitions together with a new state are assigned into the level scheme of 39Cl. The spin parity of 5/2− for the lowest negative parity state in 39Cl is reconfirmed using the combined γ transition information. These systematic observations of the negative parity states in 39Cl allow a comprehensive comparison with the theoretical descriptions. The lowest 5/2− state in 39Cl remains exotic in terms of comparisons with existing theoretical calculations and with the neighboring isotopes having similar single-particle configurations. Further experimental and theoretical investigations are suggested.

The hybrid created from the crossbreeding of European and African bees, known as the Africanised bee, has provided numerous advantages for current beekeeping. However, this new species exhibits undesirable behaviours, such as colony defence instinct and a propensity to attack en masse, which can result in serious accidents. To date, there is no effective treatment for cases of Africanised bee envenomation. One promising technique for developing an efficient antivenom is the use of phage display technology, which enables the production of human antibodies, thus avoiding the complications of serum therapy, such as anaphylaxis and serum sickness. The aim of this study was to produce human monoclonal single-chain Fv (scFv) antibody fragments capable of inhibiting the toxic effects of Africanised bee venom. We conducted four rounds of selection of antibodies against the venom and three rounds of selection of antibodies against purified melittin. Three clones were selected and tested by enzyme-linked immunosorbent assay to verify their specificity for melittin and phospholipase A2. Two clones (C5 and C12) were specific for melittin, and one (A7) was specific for phospholipase A2. In a kinetic haemolytic assay, these clones were evaluated individually and in pairs. The A7-C12 combination had the best synergistic effect and was chosen to be used in the assays of myotoxicity inhibition and lethality. The A7-C12 combination inhibited the in vivo myotoxic effect of the venom and increased the survival of treated animals.

We report an infant with intermittent urinary excretion of D-2-hydroxyglutaric (D-2-OHG) acid who died at the age of 10 months from cardiogenic shock due to cardiomyopathy. High urinary concentrations of D-2-OHG and succinic acid, as well as increased levels of lactic acid were detected on three different occasions, whereas a normal urinary profile of organic acids was found on one occasion. The clinical findings of our patient consisted of generalized hypotonia, irritability, developmental delay, generalized tonic seizures, lethargy, cardiomyopathy, and respiratory distress. Cerebral MRI revealed bilateral lesions in the substantia nigra, the periaqueductal area, the medial part of the thalamus, the hypothalamus, the caudate nucleus, putamen and globus pallidus. This pattern is suggestive of a mitochondriopathy. However, respiratory chain enzyme activities were normal in fibroblasts. Exogenous supplementation of D-2-OHG acid strongly inhibited cytochrome-c oxidase activity in fibroblasts from the patient and from normal controls in vitro. The results suggest that our patient has an unusual form of D-2-hydroxyglutaric aciduria (D-2-OHGA), different from the patients published so far, and that the increase of lactic acid and some citric acid cycle intermediates encountered in some patients with D-2-OHGA may be due to a functional defect of the respiratory chain caused by D-2-OHG acid.

A personal series (in 94% of the cases) of 102 children who underwent 170 procedures (1.66 procedures/patient) for hydrocephalus has been followed for 5 1/2 years (Jan-83 to June-88). Most of the children were under two years of age (80%) and in these cases brain sonography was the examination of choice for both diagnosis and follow-up (307 examinations, 4.4 per patient). Only occasionally was computed tomography necessary for better study in these cases. Our results suggest that there was no significant difference between our cases and those published in the literature concerning the number or procedures/patient (1.66)., infection rate (5.2%), mortality rate (6.8%) and intellectual performance. We recommend the use of brain sonography both in diagnosis and follow-up studies for hydrocephalic children since this examination is innocuous, inexpensive and easy to perform by neurosurgeons. Also it provides a good interaction between the examiner, the child and the parents, which is of utmost importance for the comprehension of the disease by the parents and early diagnosis of complications by the neurosurgeon.