Dynamical decoherence of the light induced interlayer coupling in YBa2_{2}Cu3_{3}O6+δ_{6+\delta}

Optical excitation of apical oxygen vibrations in YBa$_{2}$Cu$_{3}$O$_{6+\delta}$ has been shown to enhance its c-axis superconducting-phase rigidity, as evidenced by a transient blue shift of the equilibrium inter-bilayer Josephson plasma resonance. Surprisingly, a transient c-axis plasma mode could also be induced above T$_{c}$ by the same apical oxygen excitation, suggesting light activated superfluid tunneling throughout the pseudogap phase of YBa$_{2}$Cu$_{3}$O$_{6+\delta}$. However, despite the similarities between the above T$_{c}$ transient plasma mode and the equilibrium Josephson plasmon, alternative explanations involving high mobility quasiparticle transport should be considered. Here, we report an extensive study of the relaxation of the light-induced plasmon into the equilibrium incoherent phase. These new experiments allow for a critical assessment of the nature of this mode. We determine that the transient plasma relaxes through a collapse of its coherence length rather than its carrier (or superfluid) density. These observations are not easily reconciled with quasiparticle interlayer transport, and rather support transient superfluid tunneling as the origin of the light-induced interlayer coupling in YBa$_{2}$Cu$_{3}$O$_{6+\delta}$.Comment: 27 pages (17 pages main text, 10 pages supplementary), 5 figures (main text

Excitation dependent Fano-like interference effects in plasmonic silver nanorods

Surface plasmon resonances in metal nanoparticles are an emerging technology platform for nano-optics applications from sensing to solar energy conversion. The electromagnetic near field associated with these resonances arises from modes determined by the shape, size, and composition of the metal nanoparticle. When coupled in the near field, multiple resonant modes can interact to give rise to interference effects offering fine control of both the spectral response and spatial distribution of fields near the particle. Here, we present an examination of experimental electron energy loss spectroscopy (EELS) of silver nanorod monomer surface plasmon modes and present an explanation of observed spatial amplitude modulation of the Fabry-Pérot resonance modes of these silver nanorods using electrodynamics simulations. For these simulations, we identify differences in spectral peak symmetry in light scattering and electron spectroscopies (EELS and cathodoluminescence) and analyze the distinct near-field responses of silver nanorods to plane-wave light and electron beam excitation in terms of a coupled oscillator model. Effects of properties of the material and the incident field are evaluated, and the spatially resolved EELS signals are shown to provide a signature for assessing Fano-like interference effects in silver nanorods. These findings outline key considerations and challenges for interpreting electron microscopy data on plasmonic nanoparticles for understanding nanoscale optics and for characterization and design of photonic devices.S.M.C. acknowledges support of a Gates Cambridge Scholarship. D.R. acknowledges support from the Royal Society's Newton International Fellowship scheme. We acknowledge the use of computing facilities provided by CamGrid. Parts of this work were also performed using the Darwin Supercomputer of the University of Cambridge High Performance Computing Service (http://www.hpc.cam.ac.uk/), provided by Dell Inc. using Strategic Research Infrastructure Funding from the Higher Education Funding Council for England and funding from the Science and Technology Facilities Council. We thank F.J. de la Peña for helpful discussions on the use of hyperspy. The research leading to these results has received funding from the European Research Council under the European Union's Seventh Framework Program (Grant No. FP7/2007-2013)/ERC Grant Agreement No. 291522-3DIMAGE. Data on rod “B” were acquired by one of us (D. Rossouw) with support of a NSERC Discovery Grant (G. A. Botton) at the Canadian Centre for Electron Microscopy, a national facility supported by NSERC and McMaster University. We thank G. A. Botton for access to data on rod “B” and for helpful comments on this manuscript. P.A.M. also acknowledges funding from the European Union's Seventh Framework Program under a contract for an Integrated Infrastructure Initiative (Reference No. 312483-ESTEEM2)

Pump frequency resonances for light-induced incipient superconductivity in YBa2_2Cu3_3O6.5_{6.5}

Optical excitation in the cuprates has been shown to induce transient superconducting correlations above the thermodynamic transition temperature, $T_C$, as evidenced by the terahertz frequency optical properties in the non-equilibrium state. In YBa$_2$Cu$_3$O$_{6+x}$ this phenomenon has so far been associated with the nonlinear excitation of certain lattice modes and the creation of new crystal structures. In other compounds, like La$_{2-x}$Ba$_x$CuO$_4$, similar effects were reported also for excitation at near infrared frequencies, and were interpreted as a signature of the melting of competing orders. However, to date it has not been possible to systematically tune the pump frequency widely in any one compound, to comprehensively compare the frequency dependent photo-susceptibility for this phenomenon. Here, we make use of a newly developed optical parametric amplifier, which generates widely tunable high intensity femtosecond pulses, to excite YBa$_2$Cu$_3$O$_{6.5}$ throughout the entire optical spectrum (3 - 750 THz). In the far-infrared region (3 - 25 THz), signatures of non-equilibrium superconductivity are induced only for excitation of the 16.4 THz and 19.2 THz vibrational modes that drive $c$-axis apical oxygen atomic positions. For higher driving frequencies (25 - 750 THz), a second resonance is observed around the charge transfer band edge at ~350 THz. These observations highlight the importance of coupling to the electronic structure of the CuO$_2$ planes, either mediated by a phonon or by charge transfer.Comment: 47 pages, 21 figures, 2 table

Age-dependence of sensorimotor and cerebral electroencephalographic asymmetry in rats subjected to unilateral cerebrovascular stroke

Background: The human population mostly affected by stroke is more than 65 years old. This study was designed to meet the recommendation that models of cerebral ischemia in aged animals are more relevant to the clinical setting than young animal models. Until now the majority of the pre-clinical studies examining age effects on stroke outcomes have used rats of old age. Considering the increasing incidence of stroke among younger than old human population, new translational approaches in animal models are needed to match the rejuvenation of stroke. A better knowledge of alterations in stroke outcomes in middle-aged rats has important preventive and management implications providing clues for future investigations on effects of various neuroprotective and neurorestorative drugs against cerebrovascular accidents that may occur before late senescence. Methods: We evaluated the impact of transient focal ischemia, induced by intracerebral unilateral infusion of endothelin-1 (Et-1) near the middle cerebral artery of conscious rats, on volume of brain damage and asymmetry in behavioral and electroencephalographic (EEG) output measures in middle-aged (11-12 month-old) rats. Results: We did not find any age-dependent difference in the volume of ischemic brain damage three days after Et-1 infusion. However, age was an important determinant of neurological and EEG outcomes after stroke. Middle-aged ischemic rats had more impaired somatosensory functions of the contralateral part of the body than young ischemic rats and thus, had greater left-right reflex/sensorimotor asymmetry. Interhemispheric EEG asymmetry was more evident in middle-aged than in young ischemic rats, and this could tentatively explain the behavioral asymmetry.Conclusions: With a multiparametric approach, we have validated the endothelin model of ischemia in middle-aged rats. The results provide clues for future studies on mechanisms underlying plasticity after brain damage and motivate investigations of novel neuroprotective strategies against cerebrovascular accidents that may occur before late senescence. © 2013 Moyanova et al.; licensee BioMed Central Ltd

Comparisons of halogenated ß-nitrostyrenes as antimicrobial agents

The influence of three types of halogen-substituted E-ß-methyl-ß-nitrostyrenes (such as Compounds B, D, H) to overcome bacterial activity that is currently a significant health threat was studied. The evaluations of their bio-potency was measured and related to their structure and activity relationships for the purposes of serving to inhibit and overcoming resistant microorganisms. In particular, fluorine-containing ß-nitrostyrenes were found to be highly active antimicrobial agents. The addition of the ß-bromo group enhanced the antibacterial activity significantly. Our work has illustrated that halogen substituents at both the 4-position in the aromatic ring and also at the ß-position on the alkene side chain of nitropropenyl arenes enhanced the antimicrobial activity of these compounds

Influência da pressão na densidade e no teor de umidade de briquetes de diferentes resíduos de biomassa florestal.

Resumo

The ATLAS discovery potential for MSSM neutral Higgs bosons decaying to a mu+mu- pair in the mass range up to 130 GeV

Results are presented on the discovery potential for MSSM neutral Higgs bosons in the Mh-{max}scenario. The region of large tan beta, between 15 and 50, and mass between ~ 95 and 130 GeV is considered in the framework of the ATLAS experiment at the Large Hadron Collider (LHC), for a centre-of-mass energy = 14 TeV. This parameter region is not fully covered by the present data either from LEP or from Tevatron. The h/A bosons, supposed to be very close in mass in that region, are studied in the channel h/A -> mu+mu- accompanied by two b-jets. The study includes a method to control the most copious background, Zo -> mu+mu- accompanied by two b-jets. A possible contribution of the H boson to the signal is also considered

Downregulation of Mcl-1 has anti-inflammatory pro-resolution effects and enhances bacterial clearance from the lung

Phagocytes not only coordinate acute inflammation and host defense at mucosal sites, but also contribute to tissue damage. Respiratory infection causes a globally significant disease burden and frequently progresses to acute respiratory distress syndrome, a devastating inflammatory condition characterized by neutrophil recruitment and accumulation of protein-rich edema fluid causing impaired lung function. We hypothesized that targeting the intracellular protein myeloid cell leukemia 1 (Mcl-1) by a cyclin-dependent kinase inhibitor (AT7519) or a flavone (wogonin) would accelerate neutrophil apoptosis and resolution of established inflammation, but without detriment to bacterial clearance. Mcl-1 loss induced human neutrophil apoptosis, but did not induce macrophage apoptosis nor impair phagocytosis of apoptotic neutrophils. Neutrophil-dominant inflammation was modelled in mice by either endotoxin or bacteria (Escherichia coli). Downregulating inflammatory cell Mcl-1 had anti-inflammatory, pro-resolution effects, shortening the resolution interval (R(i)) from 19 to 7 h and improved organ dysfunction with enhanced alveolar–capillary barrier integrity. Conversely, attenuating drug-induced Mcl-1 downregulation inhibited neutrophil apoptosis and delayed resolution of endotoxin-mediated lung inflammation. Importantly, manipulating lung inflammatory cell Mcl-1 also accelerated resolution of bacterial infection (R(i); 50 to 16 h) concurrent with enhanced bacterial clearance. Therefore, manipulating inflammatory cell Mcl-1 accelerates inflammation resolution without detriment to host defense against bacteria, and represents a target for treating infection-associated inflammation

Cell cycle progression or translation control is not essential for vesicular stomatitis virus oncolysis of hepatocellular carcinoma.

The intrinsic oncolytic specificity of vesicular stomatitis virus (VSV) is currently being exploited to develop alternative therapeutic strategies for hepatocellular carcinoma (HCC). Identifying key regulators in diverse transduction pathways that define VSV oncolysis in cancer cells represents a fundamental prerequisite to engineering more effective oncolytic viral vectors and adjusting combination therapies. After having identified defects in the signalling cascade of type I interferon induction, responsible for attenuated antiviral responses in human HCC cell lines, we have now investigated the role of cell proliferation and translation initiation. Cell cycle progression and translation initiation factors eIF4E and eIF2Bepsilon have been recently identified as key regulators of VSV permissiveness in T-lymphocytes and immortalized mouse embryonic fibroblasts, respectively. Here, we show that in HCC, decrease of cell proliferation by cell cycle inhibitors or siRNA-mediated reduction of G(1) cyclin-dependent kinase activities (CDK4) or cyclin D1 protein expression, do not significantly alter viral growth. Additionally, we demonstrate that translation initiation factors eIF4E and eIF2Bepsilon are negligible in sustaining VSV replication in HCC. Taken together, these results indicate that cellular proliferation and the initiation phase of cellular protein synthesis are not essential for successful VSV oncolysis of HCC. Moreover, our observations indicate the importance of cell-type specificity for VSV oncolysis, an important aspect to be considered in virotherapy applications in the future