1,360 research outputs found
Temperature-dependent properties of the magnetic order in single-crystal BiFeO3
We report neutron diffraction and magnetization studies of the magnetic order
in multiferroic BiFeO3. In ferroelectric monodomain single crystals, there are
three magnetic cycloidal domains with propagation vectors equivalent by
crystallographic symmetry. The cycloid period slowly grows with increasing
temperature. The magnetic domain populations do not change with temperature
except in the close vicinity of the N{\P}eel temperature, at which, in
addition, a small jump in magneti- zation is observed. No evidence for the
spin-reorientation transitions proposed in previous Raman and dielectric
studies is found. The magnetic cycloid is slightly anharmonic for T=5 K. The
an- harmonicity is much smaller than previously reported in NMR studies. At
room temperature, a circular cycloid is observed, within errors. We argue that
the observed anharmonicity provides important clues for understanding
electromagnons in BiFeO3.Comment: In Press at PR
3:1 magnetization plateau and suppression of ferroelectric polarization in an Ising chain multiferroic
Ferroelectric Ising chain magnet CaCoMnO (0.96)
was studied in magnetic fields up to 33 T. Magnetization and neutron scattering
measurements reveal successive metamagnetic transitions from the zero-field
spin configuration to the state with a broad magnetization plateau, and
then to the state. The absence of
hysteresis in these plateaus reveals an intriguing coupling between the
intra-chain state and the three-dimensional geometrically frustrated magnetic
system. Inversion symmetry, broken in the state, is restored in the
state, leading to the complete suppression of the electric polarization driven
by symmetric superexchange.Comment: accepted for publication as a Brief Report in Physical Review
Sparticle masses in deflected mirage mediation
We discuss the sparticle mass patterns that can be realized in deflected
mirage mediation scenario of supersymmetry breaking, in which the moduli,
anomaly, and gauge mediations all contribute to the MSSM soft parameters.
Analytic expression of low energy soft parameters and also the sfermion mass
sum rules are derived, which can be used to interpret the experimentally
measured sparticle masses within the framework of the most general mixed
moduli-gauge-anomaly mediation. Phenomenological aspects of some specific
examples are also discussed.Comment: 43 pages, 17 figures, references adde
Loss of equilibrative nucleoside transporter 1 in mice leads to progressive ectopic mineralization of spinal tissues resembling diffuse idiopathic skeletal hyperostosis in humans
Diffuse idiopathic skeletal hyperostosis (DISH) is a noninflammatory spondyloarthropathy, characterized by ectopic calcification of spinal tissues. Symptoms include spine pain and stiffness, and in severe cases dysphagia and spinal cord compression. The etiology of DISH is unknown and there are no specific treatments. Recent studies have suggested a role for purine metabolism in the regulation of biomineralization. Equilibrative nucleoside transporter 1 (ENT1) transfers hydrophilic nucleosides, such as adenosine, across the plasma membrane. In mice lacking ENT1, we observed the development of calcified lesions resembling DISH. By 12 months of age, ENT1-/- mice exhibited signs of spine stiffness, hind limb dysfunction, and paralysis. Micro-computed tomography (μCT) revealed ectopic mineralization of paraspinal tissues in the cervical-thoracic region at 2 months of age, which extended to the lumbar and caudal regions with advancing age. Energy-dispersive X-ray microanalysis of lesions revealed a high content of calcium and phosphorus with a ratio similar to that of cortical bone. At 12 months of age, histological examination of ENT1-/- mice revealed large, irregular accumulations of eosinophilic material in paraspinal ligaments and entheses, intervertebral discs, and sternocostal articulations. There was no evidence of mineralization in appendicular joints or blood vessels, indicating specificity for the axial skeleton. Plasma adenosine levels were significantly greater in ENT1 -/- mice than in wild-type, consistent with loss of ENT1 - a primary adenosine uptake pathway. There was a significant reduction in the expression of Enpp1, Ank, and Alpl in intervertebral discs from ENT1-/- mice compared to wild-type mice. Elevated plasma levels of inorganic pyrophosphate in ENT1-/- mice indicated generalized disruption of pyrophosphate homeostasis. This is the first report of a role for ENT1 in regulating the calcification of soft tissues. Moreover, ENT1-/- mice may be a useful model for investigating pathogenesis and evaluating therapeutics for the prevention of mineralization in DISH and related disorders. © 2013 American Society for Bone and Mineral Research. Copyright © 2013 American Society for Bone and Mineral Research
Electric-field controlled spin reversal in a quantum dot with ferromagnetic contacts
Manipulation of the spin-states of a quantum dot by purely electrical means
is a highly desirable property of fundamental importance for the development of
spintronic devices such as spin-filters, spin-transistors and single-spin
memory as well as for solid-state qubits. An electrically gated quantum dot in
the Coulomb blockade regime can be tuned to hold a single unpaired spin-1/2,
which is routinely spin-polarized by an applied magnetic field. Using
ferromagnetic electrodes, however, the properties of the quantum dot become
directly spin-dependent and it has been demonstrated that the ferromagnetic
electrodes induce a local exchange-field which polarizes the localized spin in
the absence of any external fields. Here we report on the experimental
realization of this tunneling-induced spin-splitting in a carbon nanotube
quantum dot coupled to ferromagnetic nickel-electrodes. We study the
intermediate coupling regime in which single-electron states remain well
defined, but with sufficiently good tunnel-contacts to give rise to a sizable
exchange-field. Since charge transport in this regime is dominated by the
Kondo-effect, we can utilize this sharp many-body resonance to read off the
local spin-polarization from the measured bias-spectroscopy. We show that the
exchange-field can be compensated by an external magnetic field, thus restoring
a zero-bias Kondo-resonance, and we demonstrate that the exchange-field itself,
and hence the local spin-polarization, can be tuned and reversed merely by
tuning the gate-voltage. This demonstrates a very direct electrical control
over the spin-state of a quantum dot which, in contrast to an applied magnetic
field, allows for rapid spin-reversal with a very localized addressing.Comment: 19 pages, 11 figure
Axion-mediated dark matter and Higgs diphoton signal
We consider axion-mediated dark matter models motivated by Fermi gamma ray
line at 130 GeV, where anomaly interactions of an axion-like scalar mediate a
singlet Dirac fermion dark matter (DM) to electroweak gauge bosons. In these
models, extra vector-like leptons generate anomaly interactions for the axion
and can also couple to the SM Higgs boson to modify the Higgs-to-diphoton rate.
We can distinguish models by the branching fraction of the DM annihilation into
a photon pair, favoring the model with a triplet fermion. From the condition
that the lighter charged extra lepton must be heavier than dark matter for no
tree-level DM annihilations, we also show that the ratio of Higgs-to-diphoton
rate to the SM value is constrained by vacuum stability to 1.4(1.5) for the
cutoff scale of 10(1) TeV.Comment: 29 pages, 6 figures, references adde
Direct Evidence for Dominant Bond-directional Interactions in a Honeycomb Lattice Iridate Na2IrO3
Heisenberg interactions are ubiquitous in magnetic materials and have been
prevailing in modeling and designing quantum magnets. Bond-directional
interactions offer a novel alternative to Heisenberg exchange and provide the
building blocks of the Kitaev model, which has a quantum spin liquid (QSL) as
its exact ground state. Honeycomb iridates, A2IrO3 (A=Na,Li), offer potential
realizations of the Kitaev model, and their reported magnetic behaviors may be
interpreted within the Kitaev framework. However, the extent of their relevance
to the Kitaev model remains unclear, as evidence for bond-directional
interactions remains indirect or conjectural. Here, we present direct evidence
for dominant bond-directional interactions in antiferromagnetic Na2IrO3 and
show that they lead to strong magnetic frustration. Diffuse magnetic x-ray
scattering reveals broken spin-rotational symmetry even above Neel temperature,
with the three spin components exhibiting nano-scale correlations along
distinct crystallographic directions. This spin-space and real-space
entanglement directly manifests the bond-directional interactions, provides the
missing link to Kitaev physics in honeycomb iridates, and establishes a new
design strategy toward frustrated magnetism.Comment: Nature Physics, accepted (2015
Wnt5a induces ROR1 to complex with HS1 to enhance migration of chronic lymphocytic leukemia cells.
ROR1 (receptor tyrosine kinase-like orphan receptor 1) is a conserved, oncoembryonic surface antigen expressed in chronic lymphocytic leukemia (CLL). We found that ROR1 associates with hematopoietic-lineage-cell-specific protein 1 (HS1) in freshly isolated CLL cells or in CLL cells cultured with exogenous Wnt5a. Wnt5a also induced HS1 tyrosine phosphorylation, recruitment of ARHGEF1, activation of RhoA and enhanced chemokine-directed migration; such effects could be inhibited by cirmtuzumab, a humanized anti-ROR1 mAb. We generated truncated forms of ROR1 and found its extracellular cysteine-rich domain or kringle domain was necessary for Wnt5a-induced HS1 phosphorylation. Moreover, the cytoplamic, and more specifically the proline-rich domain (PRD), of ROR1 was required for it to associate with HS1 and allow for F-actin polymerization in response to Wnt5a. Accordingly, we introduced single amino acid substitutions of proline (P) to alanine (A) in the ROR1 PRD at positions 784, 808, 826, 841 or 850 in potential SH3-binding motifs. In contrast to wild-type ROR1, or other ROR1P→︀A mutants, ROR1P(841)A had impaired capacity to recruit HS1 and ARHGEF1 to ROR1 in response to Wnt5a. Moreover, Wnt5a could not induce cells expressing ROR1P(841)A to phosphorylate HS1 or activate ARHGEF1, and was unable to enhance CLL-cell motility. Collectively, these studies indicate HS1 plays an important role in ROR1-dependent Wnt5a-enhanced chemokine-directed leukemia-cell migration
A boron-coated CCD camera for direct detection of Ultracold Neutrons (UCN)
A new boron-coated CCD camera is described for direct detection of ultracold
neutrons (UCN) through the capture reactions B
(n,0)Li (6%) and B(n,1)Li (94%).
The experiments, which extend earlier works using a boron-coated ZnS:Ag
scintillator, are based on direct detections of the neutron-capture byproducts
in silicon. The high position resolution, energy resolution and particle ID
performance of a scientific CCD allows for observation and identification of
all the byproducts , Li and (electron recoils). A
signal-to-noise improvement on the order of 10 over the indirect method has
been achieved. Sub-pixel position resolution of a few microns is demonstrated.
The technology can also be used to build UCN detectors with an area on the
order of 1 m. The combination of micrometer scale spatial resolution, few
electrons ionization thresholds and large area paves the way to new research
avenues including quantum physics of UCN and high-resolution neutron imaging
and spectroscopy.Comment: 10 pages, 8 figure
High resolution chromosome 3p, 8p, 9q and 22q allelotyping analysis in the pathogenesis of gallbladder carcinoma
Our recent genome-wide allelotyping analysis of gallbladder carcinoma identified 3p, 8p, 9q and 22q as chromosomal regions with frequent loss of heterozygosity. The present study was undertaken to more precisely identify the presence and location of regions of frequent allele loss involving those chromosomes in gallbladder carcinoma. Microdissected tissue from 24 gallbladder carcinoma were analysed for PCR-based loss of heterozygosity using 81 microsatellite markers spanning chromosome 3p (n=26), 8p (n=14), 9q (n=29) and 22q (n=12) regions. We also studied the role of those allele losses in gallbladder carcinoma pathogenesis by examining 45 microdissected normal and dysplastic gallbladder epithelia accompanying gallbladder carcinoma, using 17 microsatellite markers. Overall frequencies of loss of heterozygosity at 3p (100%), 8p (100%), 9q (88%), and 22q (92%) sites were very high in gallbladder carcinoma, and we identified 13 distinct regions undergoing frequent loss of heterozygosity in tumours. Allele losses were frequently detected in normal and dysplastic gallbladder epithelia. There was a progressive increase of the overall loss of heterozygosity frequency with increasing severity of histopathological changes. Allele losses were not random and followed a sequence. This study refines several distinct chromosome 3p, 8p, 9q and 22q regions undergoing frequent allele loss in gallbladder carcinoma that will aid in the positional identification of tumour suppressor genes involved in gallbladder carcinoma pathogenesis
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