Interwoven magnetic and flux line structures in single crystal (Tm,Er)Ni2B2C

We review studies of the interactions between magnetic order and the flux line lattice (FLL) in the (RE)Ni2B2Cintermetallic borocarbides for (RE)=Tm and Er using small angle neutron scattering (SANS) and magneto-transport. For (RE)=Tm the magnetic order and the FLL assume a common symmetry, sharing a phase transition at ∼2 kOe, despite an order of magnitude difference in periodicity. For (RE)=Er, the penetration depth λ and the coherence length ξ, both of which are derived from the FLL form factor, are modified near TN=6 K by a theoretically predicted weakly divergent pairbreaking. Finally, below 2.3 K, (RE)=Er shows a coexistence of weak ferromagnetism and superconductivity. This state reveals a highly disordered FLL and a striking increase in the critical current, both arising from the strong ferromagnetic pairbreaking

The puzzle of 90 degree reorientation in the vortex lattice of borocarbide superconductors

We explain 90 degree reorientation in the vortex lattice of borocarbide superconductors on the basis of a phenomenological extension of the nonlocal London model that takes full account of the symmetry of the system. We propose microscopic mechanisms that could generate the correction terms and point out the important role of the superconducting gap anisotropy.Comment: 4 pages, 2 eps figure

Nature of 45 degree vortex lattice reorientation in tetragonal superconductors

The transformation of the vortex lattice in a tetragonal superconductor which consists of its 45 degree reorientation relative to the crystal axes is studied using the nonlocal London model. It is shown that the reorientation occurs as two successive second order (continuous) phase transitions. The transition magnetic fields are calculated for a range of parameters relevant for borocarbide superconductors in which the reorientation has been observed

Temperature Dependence of the Flux Line Lattice Transition into Square Symmetry in Superconducting LuNi2_2B2_2C

We have investigated the temperature dependence of the H || c flux line lattice structural phase transition from square to hexagonal symmetry, in the tetragonal superconductor LuNi_2B_2C (T_c = 16.6 K). At temperatures below 10 K the transition onset field, H_2(T), is only weakly temperature dependent. Above 10 K, H_2(T) rises sharply, bending away from the upper critical field. This contradicts theoretical predictions of H_2(T) merging with the upper critical field, and suggests that just below the H_c2(T)-curve the flux line lattice might be hexagonal.Comment: 4 pages, 3 figure

Tunneling spectroscopy in the magnetic superconductor TmNi2B2C

We present new measurements about the tunneling conductance in the borocarbide superconductor TmNi$_2$B$_2$C. The results show a very good agreement with weak coupling BCS theory, without any lifetime broadening parameter, over the whole sample surface. We detect no particular change of the tunneling spectroscopy below 1.5K, when both the antiferromagnetic (AF) phase and the superconducting order coexist.Comment: Submitted to Phys. Rev. B, Rapid Communication

Theory of superfluidity and drag force in the one-dimensional Bose gas

The one-dimensional Bose gas is an unusual superfluid. In contrast to higher spatial dimensions, the existence of non-classical rotational inertia is not directly linked to the dissipationless motion of infinitesimal impurities. Recently, experimental tests with ultracold atoms have begun and quantitative predictions for the drag force experienced by moving obstacles have become available. This topical review discusses the drag force obtained from linear response theory in relation to Landau's criterion of superfluidity. Based upon improved analytical and numerical understanding of the dynamical structure factor, results for different obstacle potentials are obtained, including single impurities, optical lattices and random potentials generated from speckle patterns. The dynamical breakdown of superfluidity in random potentials is discussed in relation to Anderson localization and the predicted superfluid-insulator transition in these systems.Comment: 17 pages, 12 figures, mini-review prepared for the special issue of Frontiers of Physics "Recent Progresses on Quantum Dynamics of Ultracold Atoms and Future Quantum Technologies", edited by Profs. Lee, Ueda, and Drummon

Selenoprotein gene nomenclature

The human genome contains 25 genes coding for selenocysteine-containing proteins (selenoproteins). These proteins are involved in a variety of functions, most notably redox homeostasis. Selenoprotein enzymes with known functions are designated according to these functions: TXNRD1, TXNRD2, and TXNRD3 (thioredoxin reductases), GPX1, GPX2, GPX3, GPX4 and GPX6 (glutathione peroxidases), DIO1, DIO2, and DIO3 (iodothyronine deiodinases), MSRB1 (methionine-R-sulfoxide reductase 1) and SEPHS2 (selenophosphate synthetase 2). Selenoproteins without known functions have traditionally been denoted by SEL or SEP symbols. However, these symbols are sometimes ambiguous and conflict with the approved nomenclature for several other genes. Therefore, there is a need to implement a rational and coherent nomenclature system for selenoprotein-encoding genes. Our solution is to use the root symbol SELENO followed by a letter. This nomenclature applies to SELENOF (selenoprotein F, the 15 kDa selenoprotein, SEP15), SELENOH (selenoprotein H, SELH, C11orf31), SELENOI (selenoprotein I, SELI, EPT1), SELENOK (selenoprotein K, SELK), SELENOM (selenoprotein M, SELM), SELENON (selenoprotein N, SEPN1, SELN), SELENOO (selenoprotein O, SELO), SELENOP (selenoprotein P, SeP, SEPP1, SELP), SELENOS (selenoprotein S, SELS, SEPS1, VIMP), SELENOT (selenoprotein T, SELT), SELENOV (selenoprotein V, SELV) and SELENOW (selenoprotein W, SELW, SEPW1). This system, approved by the HUGO Gene Nomenclature Committee, also resolves conflicting, missing and ambiguous designations for selenoprotein genes and is applicable to selenoproteins across vertebrates

The HMGB1-RAGE axis mediates traumatic brain injury-induced pulmonary dysfunction in lung transplantation

Traumatic brain injury (TBI) results in systemic inflammatory responses that affect the lung. This is especially critical in the setting of lung transplantation, where more than half of donor allografts are obtained postmortem from individuals with TBI. The mechanism by which TBI causes pulmonary dysfunction remains unclear but may involve the interaction of high-mobility group box-1 (HMGB1) protein with the receptor for advanced glycation end products (RAGE). To investigate the role of HMGB1 and RAGE in TBI-induced lung dysfunction, RAGE-sufficient (wild-type) or RAGE-deficient (RAGE(-/-)) C57BL/6 mice were subjected to TBI through controlled cortical impact and studied for cardiopulmonary injury. Compared to control animals, TBI induced systemic hypoxia, acute lung injury, pulmonary neutrophilia, and decreased compliance (a measure of the lungs' ability to expand), all of which were attenuated in RAGE(-/-) mice. Neutralizing systemic HMGB1 induced by TBI reversed hypoxia and improved lung compliance. Compared to wild-type donors, lungs from RAGE(-/-) TBI donors did not develop acute lung injury after transplantation. In a study of clinical transplantation, elevated systemic HMGB1 in donors correlated with impaired systemic oxygenation of the donor lung before transplantation and predicted impaired oxygenation after transplantation. These data suggest that the HMGB1-RAGE axis plays a role in the mechanism by which TBI induces lung dysfunction and that targeting this pathway before transplant may improve recipient outcomes after lung transplantation

Energy scan of the e+e−→hb(nP)π+π−e^+e^- \to h_b(nP)\pi^+\pi^- (n=1,2)(n=1,2) cross sections and evidence for Υ(11020)\Upsilon(11020) decays into charged bottomonium-like states

Using data collected with the Belle detector at the KEKB asymmetric-energy $e^+e^-$ collider, we measure the energy dependence of the $e^+e^- \to h_b(nP)\pi^+\pi^-$ $(n=1,2)$ cross sections from thresholds up to $11.02\,$GeV. We find clear $\Upsilon(10860)$ and $\Upsilon(11020)$ peaks with little or no continuum contribution. We study the resonant substructure of the $\Upsilon(11020) \to h_b(nP)\pi^+\pi^-$ transitions and find evidence that they proceed entirely via the intermediate isovector states $Z_b(10610)$ and $Z_b(10650)$. The relative fraction of these states is loosely constrained by the current data: the hypothesis that only $Z_b(10610)$ is produced is excluded at the level of 3.3 standard deviations, while the hypothesis that only $Z_b(10650)$ is produced is not excluded at a significant level.Comment: 8 pages, 4 figures, submitted to Physical Review Letter

Search for Λc+→ϕpπ0\Lambda_c^+\to\phi p \pi^0 and branching fraction measurement of Λc+→K−π+pπ0\Lambda_c^+\to K^-\pi^+ p \pi^0

We have searched for the Cabibbo-suppressed decay $\Lambda_c^+\to\phi p\pi^0$ in $e^+e^-$ collisions using a data sample corresponding to an integrated luminosity of 915 $\rm fb^{-1}$. The data were collected by the Belle experiment at the KEKB $e^+e^-$ asymmetric-energy collider running at or near the $\Upsilon(4S)$ and $\Upsilon(5S)$ resonances. No significant signal is observed, and we set an upper limit on the branching fraction of $\mathcal{B}(\Lambda_c^+\to \phi p\pi^0) <15.3\times10^{-5}$ at 90% confidence level. The contribution for nonresonant $\Lambda_c^+\to K^+K^- p\pi^0$ decays is found to be consistent with zero and the corresponding upper limit on its branching fraction is set to be $\mathcal{B}(\Lambda_c^+\to K^+K^-p\pi^0)_{\rm NR} <6.3\times10^{-5}$ at 90% confidence level. We also measure the branching fraction for the Cabibbo-favored decay $\Lambda_c^+\to K^-\pi^+p\pi^0$; the result is $\mathcal{B}(\Lambda_c^+\to K^-\pi^+p\pi^0)= (4.42\pm0.05\, (\rm stat.) \pm 0.12\, (\rm syst.) \pm 0.16\, (\mathcal{B}_{\rm Norm}))\%$, which is the most precise measurement to date. Finally, we have searched for an intermediate hidden-strangeness pentaquark decay $P^+_s\to\phi p$. We see no evidence for this intermediate decay and set an upper limit on the product branching fraction of ${\cal B}(\Lambda_c^+\to P^+_s \pi^0)\times {\cal B}(P^+_s\to\phi p) <8.3\times 10^{-5}$ at 90% confidence level.Comment: 8 pages, 5 figures, 1 table, minor text change in version