Photonic Crystal Vertical Cavity Lasers

Photonic crystal confinement in vertical cavity surface-emitting lasers (VCSELs) is a robust and reliable technology for achieving operation in the fundamental lateral mode and is potentially applicable to a variety of materials systems and operating wavelengths. We demonstrate photonic crystal VCSELs operating in a single transverse mode with over 30 dB side mode suppression and over 1 mW of output power. These lasers have been subjected to a post-process technique to introduce the etched holes making up the photonic crystals that surround a centralized defect in which lasing occurs. We also show that coupling between adjacent defects in a photonic lattice is possible, further increasing the power available in the devices

Identification of a novel retroviral gene unique to human immunodeficiency virus type 2 and simian immunodeficiency virus SIVMAC

Human and simian immunodeficiency-associated retroviruses are extraordinarily complex, containing at least five genes, tat, art, sor, R, and 3' orf, in addition to the structural genes gag, pol, and env. Recently, nucleotide sequence analysis of human immunodeficiency virus type 2 (HIV-2) and simian immunodeficiency virus SIVMAC revealed the existence of still another open reading frame, termed X, which is highly conserved between these two viruses but absent from HIV-1. In this report, we demonstrate for the first time that the X open reading frame represents a functional retroviral gene in both HIV-2 and SIVMAC and that it encodes a virion-associated protein of 14 and 12 kilodaltons, respectively. We also describe the production of recombinant TrpE/X fusion proteins in Escherichia coli and show that sera from some HIV-2-infected individuals specifically recognize these proteins

Quantum statistical metastability for a finite spin

We study quantum-classical escape-rate transitions for uniaxial and biaxial models with finite spins S=10 (such as Mn_12Ac and Fe_8) and S=100 by a direct numerical approach. At second-order transitions the level making a dominant contribution into thermally assisted tunneling changes gradually with temperature whereas at first-order transitions a group of levels is skipped. For finite spins, the quasiclassical boundaries between first- and second-order transitions are shifted, favoring a second-order transition: For Fe_8 in zero field the transition should be first order according to a theory with S \to \infty, but we show that there are no skipped levels at the transition. Applying a field along the hard axis in Fe_8 makes transition the strongest first order. For the same model with S=100 we confirmed the existence of a region where a second-order transition is followed by a first-order transition [X. Martines Hidalgo and E. M. Chudnovsky, J. Phys.: Condensed Matter (in press)].Comment: 7 Phys. Rev. pages, 10 figures, submitted to PR

Phenotypic and functional characteristics of highly differentiated CD57 +NKG2C + NK cells in HIV-1- infected individuals

Natural killer (NK) cells are important anti-viral effector cells. The function and phenotype of the NK cells that constitute an individual’s NK cell repertoire can be influenced by ongoing and/or previous viral infections. Indeed, infection with human cytomegalovirus (HCMV) drives the expansion of a highly differentiated NK cell population characterized by expression of CD57 and the activating NKG2C receptor. This NK cell population has also been noted to occur in HIV-1-infected individuals. We evaluated the NK cells of HIV-1-infected and –uninfected individuals to determine the relative frequency of highly differentiated CD57 +NKG2C + NK cells and characterize these cells for their receptor expression and responsiveness to diverse stimuli. Highly differentiated CD57 +NKG2C + NK cells occurred at higher frequencies in HCMV-infected donors relative to HCMV-uninfected donors and were dramatically expanded in HIV-1/HCMV co-infected donors. The expanded CD57 +NKG2C + NK cell population in HIV-1-infected donors remained stable following antiretroviral therapy. CD57 +NKG2C + NK cells derived from HIV-1-infected individuals were robustly activated by antibody-dependent stimuli that contained anti-HIV-1 antibodies or therapeutic anti-CD20 antibody, and these NK cells mediated cytolysis through NKG2C. Lastly, CD57 +NKG2C + NK cells from HIV-1-infected donors were characterized by reduced expression of the inhibitory NKG2A receptor. The abundance of highly functional CD57 +NKG2C + NK cells in HIV-1-infected individuals raises the possibility that these NK cells could play a role in HIV-1 pathogenesis or serve as effector cells for therapeutic/cure strategies

QMCPACK: Advances in the development, efficiency, and application of auxiliary field and real-space variational and diffusion Quantum Monte Carlo

We review recent advances in the capabilities of the open source ab initio Quantum Monte Carlo (QMC) package QMCPACK and the workflow tool Nexus used for greater efficiency and reproducibility. The auxiliary field QMC (AFQMC) implementation has been greatly expanded to include k-point symmetries, tensor-hypercontraction, and accelerated graphical processing unit (GPU) support. These scaling and memory reductions greatly increase the number of orbitals that can practically be included in AFQMC calculations, increasing accuracy. Advances in real space methods include techniques for accurate computation of band gaps and for systematically improving the nodal surface of ground state wavefunctions. Results of these calculations can be used to validate application of more approximate electronic structure methods including GW and density functional based techniques. To provide an improved foundation for these calculations we utilize a new set of correlation-consistent effective core potentials (pseudopotentials) that are more accurate than previous sets; these can also be applied in quantum-chemical and other many-body applications, not only QMC. These advances increase the efficiency, accuracy, and range of properties that can be studied in both molecules and materials with QMC and QMCPACK

LOTIS, Super-LOTIS, SDSS and Tautenburg Observations of GRB 010921

We present multi-instrument optical observations of the High Energy Transient Explorer (HETE-2)/Interplanetary Network (IPN) error box of GRB 010921. This event was the first gamma ray burst (GRB) localized by HETE-2 which has resulted in the detection of an optical afterglow. In this paper we report the earliest known observations of the GRB010921 field, taken with the 0.11-m Livermore Optical Transient Imaging System (LOTIS) telescope, and the earliest known detection of the GRB010921 optical afterglow, using the 0.5-m Sloan Digital Sky Survey Photometric Telescope (SDSS PT). Observations with the LOTIS telescope began during a routine sky patrol 52 minutes after the burst. Observations were made with the SDSS PT, the 0.6-m Super-LOTIS telescope, and the 1.34-m Tautenburg Schmidt telescope at 21.3, 21.8, and 37.5 hours after the GRB, respectively. In addition, the host galaxy was observed with the USNOFS 1.0-m telescope 56 days after the burst. We find that at later times (t > 1 day after the burst), the optical afterglow exhibited a power-law decline with a slope of $\alpha = 1.75 \pm 0.28$. However, our earliest observations show that this power-law decline can not have extended to early times (t < 0.035 day).Comment: AASTeX v5.x LaTeX 2e, 6 pages with 2 postscript figures, will be submitted to ApJ Letter

The magnitude and timing of recalled immunity after breakthrough infection is shaped by SARS-CoV-2 variants

Vaccination against SARS-CoV-2 protects from infection and improves clinical outcomes in breakthrough infections, likely reflecting residual vaccine-elicited immunity and recall of immunological memory. Here, we define the early kinetics of spike-specific humoral and cellular immunity after vaccination of seropositive individuals and after Delta or Omicron breakthrough infection in vaccinated individuals. Early longitudinal sampling revealed the timing and magnitude of recall, with the phenotypic activation of B cells preceding an increase in neutralizing antibody titers. While vaccination of seropositive individuals resulted in robust recall of humoral and T cell immunity, recall of vaccine-elicited responses was delayed and variable in magnitude during breakthrough infections and depended on the infecting variant of concern. While the delayed kinetics of immune recall provides a potential mechanism for the lack of early control of viral replication, the recall of antibodies coincided with viral clearance and likely underpins the protective effects of vaccination against severe COVID-19