Robust pinning of magnetic moments in pyrochlore iridates

Pyrochlore iridates A2Ir2O7 (A = rare earth elements, Y or Bi) hold great promise for realizing novel electronic and magnetic states owing to the interplay of spin-orbit coupling, electron correlation and geometrical frustration. A prominent example is the formation of all-in/all-out (AIAO)antiferromagnetic order in the Ir4+ sublattice that comprises of corner-sharing tetrahedra. Here we report on an unusual magnetic phenomenon, namely a cooling-field induced shift of magnetic hysteresis loop along magnetization axis, and its possible origin in pyrochlore iridates with non-magnetic Ir defects (e.g. Ir3+). In a simple model, we attribute the magnetic hysteresis loop to the formation of ferromagnetic droplets in the AIAO antiferromagnetic background. The weak ferromagnetism originates from canted antiferromagnetic order of the Ir4+ moments surrounding each non-magnetic Ir defect. The shift of hysteresis loop can be understood quantitatively based on an exchange-bias like effect in which the moments at the shell of the FM droplets are pinned by the AIAO AFM background via mainly the Heisenberg (J) and Dzyaloshinsky-Moriya (D) interactions. The magnetic pinning is stable and robust against the sweeping cycle and sweeping field up to 35 T, which is possibly related to the magnetic octupolar nature of the AIAO order.Comment: 16 pages, 4 figure

In vitro assessment of the toxicity of lead (Pb2+) to phycocyanin

© 2017 Elsevier Ltd This work reports the influence of lead (Pb2+) on fluorescence characteristics and protein structure of phycocyanin molecules experimentally in vitro. The fluorescence intensity decreases with the increasing concentration of Pb2+ from 0 to 5 × 10−5 mol L−1, showing the fluorescence quenching of phycocyanin by Pb2+. The quenching process is suggested to be static regarding the calculation results and the experimental results of time-resolved fluorescence decay profiles. The synchronous fluorescence spectra show that the effect of Pb2+ on the Tyr residues of phycocyanin is more significant than the Trp residues. The forming of aggregation by the interaction of Pb2+ with phycocyanin molecules is suggested from the results of resonance light scattering spectra. The UV–Vis spectra of the protein skeleton of phycocyanin have a red-shift of about 10 nm with increasing the Pb2+ concentration from 0 to 5 × 10−5 mol L−1, indicating a change in the protein skeleton and its secondary structure. With the increasing Pb2+ concentration, the two negative peaks (209 nm and 218 nm) on circular dichroism spectra become smaller, showing a decrease of the α-helix structure. These results may give people a deeper understanding of that how the heavy metal (Pb2+) can affect the chemo-physical properties of phycocyanin

Dexmedetomidine Pretreatment Attenuates Kidney Injury and Oxidative Stress during Orthotopic Autologous Liver Transplantation in Rats

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Bias-Dependent Generation and Quenching of Defects in Pentacene

We describe a defect in pentacene single crystals that is created by bias stress and persists at room temperature for an hour in the dark but only seconds with 420nm illumination. The defect gives rise to a hole trap at Ev + 0.38eV and causes metastable transport effects at room temperature. Creation and decay rates of the hole trap have a 0.67eV activation energy with a small (108 s-1) prefactor, suggesting that atomic motion plays a key role in the generation and quenching process.Comment: 10 pages, 3 figure

BL Lacertae are probable sources of the observed ultra-high energy cosmic rays

We calculate angular correlation function between ultra-high energy cosmic rays (UHECR) observed by Yakutsk and AGASA experiments, and most powerful BL Lacertae objects. We find significant correlations which correspond to the probability of statistical fluctuation less than $10^{-4}$, including penatly for selecting the subset of brightest BL Lacs. We conclude that some of BL Lacs are sources of the observed UHECR and present a list of most probable candidates.Comment: Replaced with the version accepted for publication in JETP Let

Aislamiento y análisis de la expresión del gen aciltransferasa glicerol-3-fosfato de cacahuete (Arachis hypogaea L.)

sn-Glycerol-3-phosphate acyltransferase (GPAT) catalyzes the committed step in the production of glycerolipids. The functions of GPAT genes have been intensively studied in Arabidopsis, but not in peanuts (Arachis hypogaea L.). In this study, six AhGPAT genes were isolated from peanuts. Quantitative real-time RT-PCR analysis indicated that the AhGPAT9 transcript was more abundant in the stems, flowers, and seeds, whereas the transcript abundances of five other genes were higher in the leaves or flowers than in the other tissues examined. During seed development, the transcript levels of AhGPAT9 gradually increased, whereas the transcript levels of the other five genes decreased. In addition, the levels of AhGPAT2 transcript were distinctly enhanced after exposure to all four kinds of stress treatments except for ABA-treated leaves. The transcripts of AhGPAT1, AhGPAT6, AhGPAT8 and AhATS1 increased substantially in roots exposed to salt, drought, and ABA stress. The expressions of AhGPAT6, AhGPAT8, AhGPAT9 and AhATS1 were slightly higher in leaves under certain stress conditions than under normal conditions. The present study provides significant information for modifying oil deposition and improving the abiotic stress resistance of peanuts through molecular breeding.La aciltransferasa sn-glicerol-3-fosfato (ATGP) cataliza el comprometido paso de la producción de glicerolípidos. Las funciones de los genes AhATGP se han estudiado intensivamente en Arabidopsis, pero no en cacahuete (Arachis hypogaea L.). En este estudio, seis genes AhATGP se aislaron a partir de cacahuetes. El análisis a tiempo real RT-PCR cuantitativa indicó que la transcripción AhATGP9 fue más abundante en tallos, flores y semillas, mientras que la abundancia de la transcripción de los otros cinco genes fueron mayores en hojas o flores que en los otros tejidos examinados. Durante el desarrollo de la semilla, los niveles de transcripción de AhATGP9 aumentaron gradualmente, mientras que los niveles de transcripción de otros cinco genes disminuyeron. Además, los niveles de transcripción AhATGP2 mejoraron claramente después de la exposición a los cuatro tipos de tratamientos de estrés excepto para las hojas tratadas con ABA. Las transcripciones de ATGP1, ATGP6, ATGP8 y AhATS1 aumentaron considerablemente en las raíces expuestas a sal, sequía y estrés de ABA. Las expresiones de AhGPAT6, AhGPAT8, AhGPAT9 y AhATS1 fueron ligeramente más altos en las hojas bajo ciertas condiciones de estrés que en condiciones normales. El presente estudio proporciona información importante para utilizar en la modificación de la acumulación de aceite y mejorar la resistencia al estrés abiótico de maní a través de mejoramiento molecular

Search for D to phi l nu and measurement of the branching fraction for D to phi pi

Using a data sample of integrated luminosity of about 33 pb$^{-1}$ collected around 3.773 GeV with the BESII detector at the BEPC collider, the semileptonic decays $D^+ \to \phi e ^+\nu_e$, $D^+ \to \phi \mu^+\nu_\mu$ and the hadronic decay $D^+ \to \phi \pi^+$ are studied. The upper limits of the branching fractions are set to be $BF(D^+ \to \phi e ^+\nu_e) <$ 2.01% and $BF(D^+ \to \phi \mu^+ \nu_\mu) <$ 2.04% at the 90% confidence level. The ratio of the branching fractions for $D^+ \to \phi \pi^+$ relative to $D^+ \to K^-\pi^+\pi^+$ is measured to be $0.057 \pm 0.011 \pm 0.003$. In addition, the branching fraction for $D^+ \to \phi \pi^+$ is obtained to be $(5.2 \pm 1.0 \pm 0.4) \times 10^{-3}$.Comment: 6 pages, 5 figures, to be published in Eur.Phys.J.

Measurements of branching fractions for inclusive K0~/K0 and K*(892)+- decays of neutral and charged D mesons

Using the data sample of about 33 pb-1 collected at and around 3.773 GeV with the BES-II detector at the BEPC collider, we have studied inclusive K0~/K0 and K*(892)+- decays of D0 and D+ mesons. The branching fractions for the inclusive K0~/K0 and K*(892)- decays are measured to be BF(D0 to K0~/K0 X)=(47.6+-4.8+-3.0)%, BF(D+ to K0~/K0 X)=(60.5+-5.5+-3.3)%, BF(D0 to K*- X)=(15.3+- 8.3+- 1.9)% and BF(D+ to K*- X)=(5.7+- 5.2+- 0.7)%. The upper limits of the branching fractions for the inclusive K*(892)+ decays are set to be BF(D0 to K*+ X)<3.6% and BF(D+ to K*+ X) <20.3% at 90% confidence level