Thermalization of magnons in yttrium-iron garnet: nonequilibrium functional renormalization group approach

Using a nonequilibrium functional renormalization group (FRG) approach we calculate the time evolution of the momentum distribution of a magnon gas in contact with a thermal phonon bath. As a cutoff for the FRG procedure we use a hybridization parameter {\Lambda} giving rise to an artificial damping of the phonons. Within our truncation of the FRG flow equations the time evolution of the magnon distribution is obtained from a rate equation involving cutoff-dependent nonequilibrium self-energies, which in turn satisfy FRG flow equations depending on cutoff-dependent transition rates. Our approach goes beyond the Born collision approximation and takes the feedback of the magnons on the phonons into account. We use our method to calculate the thermalization of a quasi two-dimensional magnon gas in the magnetic insulator yttrium-iron garnet after a highly excited initial state has been generated by an external microwave field. We obtain good agreement with recent experiments.Comment: 16 pages, 6 figures, final versio

Phonon-induced disorder in dynamics of optically pumped metals from non-linear electron-phonon coupling

The non-equilibrium dynamics of matter excited by light may produce electronic phases that do not exist in equilibrium, such as laser-induced high-$T_c$ superconductivity. Here we simulate the dynamics of a metal driven at $t=0$ by a pump that excites dipole-active vibrational modes that couple quadratically to electrons, and study the evolution of its electronic and vibrational observables. We provide evidence for enhancement of local electronic correlations, including double occupancy, accompanied by rapid loss of long-range spatial phase coherence. Concurrently, the onsite vibrational reduced density matrix evolves from its initial coherent state to one with a predominantly diagonal structure whose distribution qualitatively resembles the coherent state Poisson character. This rapid loss of coherence controls the electronic dynamics as the system evolves towards a correlated electron-phonon long-time state. We show that a simple model based on an effective disorder potential generated by the oscillator dephasing dynamics for the electrons provides an explanation for the flattening in momentum of electronic correlations. Our results provide a basis within which to understand correlation dynamics of vibrationally coupled electrons in pump-probe experiments.Comment: 7 pages main text + 3 pages appendices, 5 figures main text + 2 figures appendice

Mediat. Inflamm.

There is increasing evidence that proteasomes have a biological role in the extracellular alveolar space, but inflammation could change their composition. We tested whether immunoproteasome protein-containing subpopulations are present in the alveolar space of patients with lung inflammation evoking the acute respiratory distress syndrome (ARDS). Bronchoalveolar lavage (BAL) supernatants and cell pellet lysate from ARDS patients (n = 28) and healthy subjects (n = 10) were analyzed for the presence of immunoproteasome proteins (LMP2 and LMP7) and proteasome subtypes by western blot, chromatographic purification, and 2D-dimensional gelelectrophoresis. In all ARDS patients but not in healthy subjects LMP7 and LMP2 were observed in BAL supernatants. Proteasomes purified from pooled ARDS BAL supernatant showed an altered enzyme activity ratio. Chromatography revealed a distinct pattern with 7 proteasome subtype peaks in BAL supernatant of ARDS patients that differed from healthy subjects. Total proteasome concentration in BAL supernatant was increased in ARDS (971 ng/mL perpendicular to 1116 versus 59 perpendicular to 25; P < 0.001), and all fluorogenic substrates were hydrolyzed, albeit to a lesser extent, with inhibition by epoxomicin (P = 0.0001). Thus, we identified for the first time immunoproteasome proteins and a distinct proteasomal subtype pattern in the alveolar space of ARDS patients, presumably in response to inflammation

Constraining the Hadronic Contributions to the Muon Anomalous Magnetic Moment

The mini-proceedings of the Workshop on "Constraining the hadronic contributions to the muon anomalous magnetic moment" which included the "13th meeting of the Radio MonteCarLow WG" and the "Satellite meeting R-Measurements at BES-III" held in Trento from April 10th to 12th, 2013, are presented. This collaboration meeting aims to bring together the experimental e+e- collider communities from BaBar, Belle, BESIII, CMD2, KLOE, and SND, with theorists working in the fields of meson transitions form factors, hadronic contributions to (g-2)_\mu and effective fine structure constant, and development of Monte Carlo generator and Radiative Corrections for precision e+e- and tau physics.Comment: 45 pages, 17 contributions. Editors: P. Masjuan and G. Venanzon

The nature of iron-oxygen vacancy defect centers in PbTiO3

The iron(III) center in ferroelectric PbTiO3 together with an oxygen vacancy forms a charged defect associate, oriented along the crystallographic c-axis. Its microscopic structure has been analyzed in detail comparing results from a semi-empirical Newman superposition model analysis based on finestructure data and from calculations using density functional theory. Both methods give evidence for a substitution of Fe3+ for Ti4+ as an acceptor center. The position of the iron ion in the ferroelectric phase is found to be similar to the B-site in the paraelectric phase. Partial charge compensation is locally provided by a directly coordinated oxygen vacancy. Using high-resolution synchrotron powder diffraction, it was verified that lead titanate remains tetragonal down to 12 K, exhibiting a c/a-ratio of 1.0721.Comment: 11 pages, 5 figures, accepted in Phys. Rev.

Exome Sequence Analysis of 14 Families With High Myopia

PURPOSE: To identify causal gene mutations in 14 families with autosomal dominant (AD) high myopia using exome sequencing. METHODS: Select individuals from 14 large Caucasian families with high myopia were exome sequenced. Gene variants were filtered to identify potential pathogenic changes. Sanger sequencing was used to confirm variants in original DNA, and to test for disease cosegregation in additional family members. Candidate genes and chromosomal loci previously associated with myopic refractive error and its endophenotypes were comprehensively screened. RESULTS: In 14 high myopia families, we identified 73 rare and 31 novel gene variants as candidates for pathogenicity. In seven of these families, two of the novel and eight of the rare variants were within known myopia loci. A total of 104 heterozygous nonsynonymous rare variants in 104 genes were identified in 10 out of 14 probands. Each variant cosegregated with affection status. No rare variants were identified in genes known to cause myopia or in genes closest to published genome-wide association study association signals for refractive error or its endophenotypes. CONCLUSIONS: Whole exome sequencing was performed to determine gene variants implicated in the pathogenesis of AD high myopia. This study provides new genes for consideration in the pathogenesis of high myopia, and may aid in the development of genetic profiling of those at greatest risk for attendant ocular morbidities of this disorder