Effects of Uniaxial Stress on Antiferromagnetic Moment in the Heavy Electron Compound URu_2Si_2

We have performed the elastic neutron scattering experiments under uniaxial stress \sigma along the tetragonal [100], [110] and [001] directions for URu2Si2. For \sigma // [100] and [110], the antiferromagnetic moment \mu_o is strongly enhanced from 0.02 \mu_B (\sigma=0) to 0.22 \mu_B (\sigma=2.5 kbar) at 1.5 K. The rate of increase d\mu_o/d\sigma is roughly estimated to be ~ 0.1 \mu_B/kbar, which is much larger than that for the hydrostatic pressure (~ 0.025 \mu_B/kbar). Above 2.5 kbar, \mu_o shows a tendency to saturate similar to the behavior in the hydrostatic pressure. For \sigma // [001], on the other hand, \mu_o shows only a slight increase to 0.028 \mu_B (\sigma = 4.6 kbar) with a rate of ~ 0.002 \mu_B/kbar. The observed anisotropy suggests that the competition between the hidden order and the antiferromagnetic state in URu2Si2 is strongly coupled with the tetragonal four-fold symmetry and the c/a ratio, or both.Comment: 3 pages, 3 eps figures, Proceedings of Int. Conf. on Strongly Correlated Electrons with Orbital Degrees of Freedom (Sendai, Japan, September 11-14, 2001

Specific Heat of URu2_{2}Si2_{2} in Fields to 42 T: Clues to the 'Hidden Order'

The large $\Delta$C observed at 17.5 K in URu$_{2}$Si$_{2}$ is inconsistent with the small, 0.04 $\mu_{B}$ moment measured for the antiferromagnetism observed starting (perhaps coincidentally) at the same temperature. We report measurements of this specific heat transition, thought to be due to some 'hidden order', in magnetic fields between 24 and 42 T, i. e. through the field region where three metamagnetic transtions are known to occur at 35.8, 37.3, and 39.4 T. The response of $\Delta$C in single crystal URu$_{2}$Si$_{2}$ to magnetic field, which includes a change to $\Delta$C being possibly associated with a first order phase transition for high fields, is analyzed to shed further light on the possible explanations of this unknown ordering process. At fields above 35 T, a new high field phase comes into being; the connection between this high field phase revealed by the specific heat and earlier magnetization data is discussed

Hidden Orbital Order in URu2Si2URu_{2}Si_{2}

When matter is cooled from high temperatures, collective instabilities develop amongst its constituent particles that lead to new kinds of order. An anomaly in the specific heat is a classic signature of this phenomenon. Usually the associated order is easily identified, but sometimes its nature remains elusive. The heavy fermion metal $URu_2Si_2$ is one such example, where the order responsible for the sharp specific heat anomaly at $T_0=17 K$ has remained unidentified despite more than seventeen years of effort. In $URu_{2}Si_{2}$, the coexistence of large electron-electron repulsion and antiferromagnetic fluctuations in $URu_2Si_2$ leads to an almost incompressible heavy electron fluid, where anisotropically paired quasiparticle states are energetically favored. In this paper we use these insights to develop a detailed proposal for the hidden order in $URu_2Si_2$. We show that incommensurate orbital antiferromagnetism, associated with circulating currents between the uranium ions, can account for the local fields and entropy loss observed at the $17 K$ transition; furthermore we make detailed predictions for neutron scattering measurements

Neutron Scattering Study on Competition between Hidden Order and Antiferromagnetism in U(Ru_{1-x}Rh_x)_2Si_2 (x <= 0.05)

We have performed elastic and inelastic neutron scattering experiments on the solid solutions U(Ru_{1-x}Rh_x)_2Si_2 for the Ru rich concentrations: x=0, 0.01, 0.02, 0.025, 0.03, 0.04 and 0.05. Hidden order is suppressed with increasing x, and correspondingly the onset temperature T_m (~ 17.5 K at x=0) of weak antiferromagnetic (AF) Bragg reflection decreases. For x=0.04 and 0.05, no magnetic order is detected in the investigated temperature range down to 1.4 K. In the middle range, 0.02 <= x <= 0.03, we found that the AF Bragg reflection is strongly enhanced. At x=0.02, this takes place at ~ 7.7 K (=T_M), which is significantly lower than T_m (~ 13.7 K). T_M increases with increasing x, and seems to merge with T_m at x=0.03. If the AF state is assumed to be homogeneous, the staggered moment \mu_o estimated at 1.4 K increases from 0.02(2) \mu_B/U (x=0) to 0.24(1) \mu_B/U (x=0.02). The behavior is similar to that observed under hydrostatic pressure (\mu_o increases to ~ 0.25 \mu_B/U at 1.0 GPa), suggesting that the AF evolution induced by Rh doping is due to an increase in the AF volume fraction. We also found that the magnetic excitation observed at Q=(1,0,0) below T_m disappears as T is lowered below T_M.Comment: 4 pages, 4 figures, submitted to J. Phys. Soc. Jp

Evolution of Heterogeneous Antiferromagnetic State in URu2Si2: Study of Hydrostatic-Pressure, Uniaxial-Stress and Rh-Dope Effects

We have investigated the nature of the competition between hidden order and antiferromagnetic (AF) order in URu_2Si_2 by performing the neutron scattering experiments under hydrostatic-pressure P, uniaxial-stress sigma, and Rh-substitution conditions. Hidden order observed at ambient pressure in pure URu_2Si_2 is found to be replaced by the AF order by applying P, sigma along the tetragonal basal plane, and by doping Rh. We discuss these experimental results on the basis of the crystalline strain calculations, and suggest that this phase transition is generated by the 0.1% increase of the tetragonal c/a ratio. We have also found that the magnetic excitation observed in the hidden order phase vanishes in the AF phase. We show that this variation can be qualitatively explained by assuming the hidden order parameter to be quadrupole.Comment: 4 pages, 4 figures, proceedings of workshop on Novel Pressure-Induced Phenomena In Condensed Matter Systems, 2006 Fukuok

Effect of Pressure on Tiny Antiferromagnetic Moment in the Heavy-Electron Compound URu_2Si_2

We have performed elastic neutron-scattering experiments on the heavy-electron compound URu_2Si_2 for pressure P up to 2.8 GPa. We have found that the antiferrmagnetic (100) Bragg reflection below T_m ~ 17.5 K is strongly enhanced by applying pressure. For P < 1.1 GPa, the staggered moment mu_o at 1.4 K increases linearly from ~ 0.017(3) mu_B to ~ 0.25(2) mu_B, while T_m increases slightly at a rate ~ 1 K/GPa, roughly following the transition temperature T_o determined from macroscopic anomalies. We have also observed a sharp phase transition at P_c ~ 1.5 GPa, above which a 3D-Ising type of antiferromagnetic phase (mu_o ~ 0.4 mu_B) appears with a slightly reduced lattice constant.Comment: RevTeX, 4 pages, 4 eps figures, accepted for publication in Phys. Rev. Let

Resonant X-Ray Scattering from URu_{2}Si_{2}

Based on a localized crystal electric field model for the U^{4+} in the (5f)^2-configuration, we analyze the resonant x-ray scattering spectra around U M_{IV} and M_{V} edges in URu_{2}Si_{2}, taking full Coulomb and spin-orbit interactions into account. We consider two level schemes, a singlet model of Santini and Amoretti and a doublet model of Ohkawa and Shimizu, and assume the antiferroquadrupolar order and the antiferromagnetic order as candidates for the ambient pressure phase and the high pressure phase. It is found that the spectral shapes as a function of photon energy are independent of the assumed level scheme, but are quite different between the antiferroquadrupole and antiferromagnetic phases, This may be useful to determine the character of the ordered phase.Comment: 8 pages, 5 figures, submitted to JPS

Bisecting GlcNAc Is a General Suppressor of Terminal Modification of N-glycan

Glycoproteins are decorated with complex glycans for protein functions. However, regulation mechanisms of complex glycan biosynthesis are largely unclear. Here we found that bisecting GlcNAc, a branching sugar residue in N-glycan, suppresses the biosynthesis of various types of terminal epitopes in N-glycans, including fucose, sialic acid and human natural killer-1. Expression of these epitopes in N-glycan was elevated in mice lacking the biosynthetic enzyme of bisecting GlcNAc, GnT-III, and was conversely suppressed by GnT-III overexpression in cells. Many glycosyltransferases for N-glycan terminals were revealed to prefer a nonbisected N-glycan as a substrate to its bisected counterpart, whereas no up-regulation of their mRNAs was found. This indicates that the elevated expression of the terminal N-glycan epitopes in GnT-III-deficient mice is attributed to the substrate specificity of the biosynthetic enzymes. Molecular dynamics simulations further confirmed that nonbisected glycans were preferentially accepted by those glycosyltransferases. These findings unveil a new regulation mechanism of protein N-glycosylation.This work was supported by Grant-in-Aid for Scientific Research (C) to Y.K. [17K07356], Leading Initiative for Excellent Young Researchers (LEADER) project to Y.K. from the Japan Society for the Promotion of Science (JSPS), by Takeda Science Foundation, and by Mochida Memorial Foundation for Medical and Pharmaceutical Research

Fermi-liquid instabilities at magnetic quantum phase transitions

This review discusses instabilities of the Fermi-liquid state of conduction electrons in metals with particular emphasis on magnetic quantum critical points. Both the existing theoretical concepts and experimental data on selected materials are presented; with the aim of assessing the validity of presently available theory. After briefly recalling the fundamentals of Fermi-liquid theory, the local Fermi-liquid state in quantum impurity models and their lattice versions is described. Next, the scaling concepts applicable to quantum phase transitions are presented. The Hertz-Millis-Moriya theory of quantum phase transitions is described in detail. The breakdown of the latter is analyzed in several examples. In the final part experimental data on heavy-fermion materials and transition-metal alloys are reviewed and confronted with existing theory.Comment: 62 pages, 29 figs, review article for Rev. Mod. Phys; (v2) discussion extended, refs added; (v3) shortened; final version as publishe

Consolidating metabolite identifiers to enable contextual and multi-platform metabolomics data analysis

<p>Abstract</p> <p>Background</p> <p>Analysis of data from high-throughput experiments depends on the availability of well-structured data that describe the assayed biomolecules. Procedures for obtaining and organizing such meta-data on genes, transcripts and proteins have been streamlined in many data analysis packages, but are still lacking for metabolites. Chemical identifiers are notoriously incoherent, encompassing a wide range of different referencing schemes with varying scope and coverage. Online chemical databases use multiple types of identifiers in parallel but lack a common primary key for reliable database consolidation. Connecting identifiers of analytes found in experimental data with the identifiers of their parent metabolites in public databases can therefore be very laborious.</p> <p>Results</p> <p>Here we present a strategy and a software tool for integrating metabolite identifiers from local reference libraries and public databases that do not depend on a single common primary identifier. The program constructs groups of interconnected identifiers of analytes and metabolites to obtain a local metabolite-centric SQLite database. The created database can be used to map in-house identifiers and synonyms to external resources such as the KEGG database. New identifiers can be imported and directly integrated with existing data. Queries can be performed in a flexible way, both from the command line and from the statistical programming environment R, to obtain data set tailored identifier mappings.</p> <p>Conclusions</p> <p>Efficient cross-referencing of metabolite identifiers is a key technology for metabolomics data analysis. We provide a practical and flexible solution to this task and an open-source program, the metabolite masking tool (MetMask), available at <url>http://metmask.sourceforge.net</url>, that implements our ideas.</p