Free-carrier screening of polarization fields in wurtzite GaN/InGaN laser structures

The free-carrier screening of macroscopic polarization fields in wurtzite GaN/InGaN quantum wells lasers is investigated via a self-consistent tight-binding approach. We show that the high carrier concentrations found experimentally in nitride laser structures effectively screen the built-in spontaneous and piezoelectric polarization fields, thus inducing a ``field-free'' band profile. Our results explain some heretofore puzzling experimental data on nitride lasers, such as the unusually high lasing excitation thresholds and emission blue-shifts for increasing excitation levels.Comment: RevTeX 4 pages, 4 figure

A 22 Degree Tidal Tail for Palomar 5

Using Data Release 4 of the Sloan Digital Sky Survey, we have applied an optimal contrast, matched filter technique to trace the trailing tidal tail of the globular cluster Palomar 5 to a distance of 18.5 degrees from the center of the cluster. This more than doubles the total known length of the tail to some 22 degrees on the sky. Based on a simple model of the Galaxy, we find that the stream's orientation on the sky is consistent at the 1.7 sigma level with existing proper motion measurements. We find that a spherical Galactic halo is adequate to model the stream over its currently known length, and we are able to place new constraints on the current space motion of the cluster.Comment: 10 pages, 3 figures, accepted for publication in ApJ Letter

Chiral perturbation theory for partially quenched twisted mass lattice QCD

Partially quenched Quantum Chromodynamics with Wilson fermions on a lattice is considered in the framework of chiral perturbation theory. Two degenerate quark flavours are associated with a chirally twisted mass term. The pion masses and decay constants are calculated in next-to-leading order including terms linear in the lattice spacing $a$.Comment: 7 pages, LaTeX2e, final published versio

On the X-ray variability of magnetar 1RXS J170849.0-400910

We present a long-term X-ray flux and spectral analysis for 1RXS J170849.0-400910 using Swift/XRT spanning over 8 years from 2005-2013. We also analyze two observations from Chandra and XMM in the period from 2003-2004. In this 10-yr period, 1RXS J170849.0-400910 displayed several rotational glitches. Previous studies have claimed variations in the X-ray emission associated with some of the glitches. From our analysis we find no evidence for significant X-ray flux variations and evidence for only low-level spectral variations. We also present an updated timing solution for 1RXS J170849.0-400910, from RXTE and Swift observations, which includes a previously unreported glitch at MJD 56019. We discuss the frequency and implications of radiatively quiet glitches in magnetars.Comment: 9 pages, 2 figures, accepted for publication in Ap

Mutations of the ret protooncogene in German multiple endocrine neoplasia families: Relation between genotype and phenotype.

It has been suggested that not only the position but also the nature of the mutations of the ret protooncogene strongly correlate with the clinical manifestation of the multiple endocrine neoplasm type 2 (MEN 2) syndrome. In particular, individuals with a Cys634-Arg substitution should have a greater risk of developing parathyroid disease. We, therefore, analyzed 94 unrelated families from Germany with inherited medullary thyroid carcinoma (MTC) for mutation of the ret protooncogene. In all but 1 of 59 families with MEN 2A, germline mutations in the extracellular domain of the ret protein were found. Some 81% of the MEN 2A mutations affected codon 634. Phenotype-genotype correlations suggested that the prevalence of pheochromocytoma and hyperparathyroidism is significantly higher in families with codon 634 mutations, but there was no correlation with the nature of the mutation. In all but 1 of 27 familial MTC (FMTC) families, mutations were detected in 1 of 4 cysteines in the extracellular domain of the ret protooncogene. Half of the FMTC mutations affected codon 634. Mutations outside of codon 634 occurred more often in FMTC families than in MEN 2A families. In all but 1 of 8 MEN 2B patients, de novo mutations in codon 918 were found. These data confirm the preferential localization of MEN 2-associated mutations and the correlation between disease phenotype and the position of the ret mutation, but there was no correlation between the occurrence of hyperparathyroidism or pheochromocytoma and the nature of the mutation