Parity-dependent State Engineering and Tomography in the ultrastrong coupling regime

Reaching the strong coupling regime of light-matter interaction has led to an impressive development in fundamental quantum physics and applications to quantum information processing. Latests advances in different quantum technologies, like superconducting circuits or semiconductor quantum wells, show that the ultrastrong coupling regime (USC) can also be achieved, where novel physical phenomena and potential computational benefits have been predicted. Nevertheless, the lack of effective decoupling mechanism in this regime has so far hindered control and measurement processes. Here, we propose a method based on parity symmetry conservation that allows for the generation and reconstruction of arbitrary states in the ultrastrong coupling regime of light-matter interactions. Our protocol requires minimal external resources by making use of the coupling between the USC system and an ancillary two-level quantum system.Comment: Improved version. 9 pages, 5 figure

Magnetic order, spin waves and fluctuations in the triangular antiferromagnet La2Ca2MnO7

We report magnetic susceptibility, specific heat and muon spin relaxation (muSR) experiments on the triangular antiferromagnet La2Ca2MnO7 which develops a genuine two-dimensional, three-sublattice \sqrt{3} \times \sqrt{3} magnetic order below T_N = 2.8 K. From the susceptibility and specific heat data an estimate of the exchange interaction is derived. A value for the spin-wave gap is obtained from the latter data. The analysis of a previously reported inelastic neutron scattering study yields values for the exchange and spin-wave gap compatible with the results obtained from macroscopic measurements. An appreciable entropy is still missing at 10 K that may be ascribed to intense short-range correlations. The critical paramagnetic fluctuations extend far above T_N, and can be partly understood in terms of two-dimensional spin-wave excitations. While no spontaneous muSR field is observed below T_N, persistent spin dynamics is found. Short-range correlations are detected in this temperature range. Their relation to a possible molecular spin substructure and the observed exotic spin fluctuations is discussed.Comment: 9 pages, 6 figure

Forest Resources Digital Information System

Forestry Images, the digitized documented forest health image archive, was developed with the aim to gather, create, maintain, and distribute digital information as tools to enhance and complement information exchange and educational activities. The Forestry Images System exists under the umbrella of Bugwood Network (Bargeron, Douce, & Moorhead, 2000). The increased volume of images and its usage statistics required major changes to enhance the system access, better content management, and security. The enhanced system is standard compliant based on recommendations from the World Wide Web Consortium (W3C) and the U.S. government Section 508

Localization of a 64-kDa phosphoprotein in the lumen between the outer and inner envelopes of pea chloroplasts

The identification and localization of a marker protein for the intermembrane space between the outer and inner chloroplast envelopes is described. This 64-kDa protein is very rapidly labeled by [γ-32P]ATP at very low (30 nM) ATP concentrations and the phosphoryl group exhibits a high turnover rate. It was possible to establish the presence of the 64-kDa protein in this plastid compartment by using different chloroplast envelope separation and isolation techniques. In addition comparison of labeling kinetics by intact and hypotonically lysed pea chloroplasts support the localization of the 64-kDa protein in the intermembrane space. The 64-kDa protein was present and could be labeled in mixed envelope membranes isolated from hypotonically lysed plastids. Mixed envelope membranes incorporated high amounts of 32P from [γ-32P]ATP into the 64-kDa protein, whereas separated outer and inner envelope membranes did not show significant phosphorylation of this protein. Water/Triton X-114 phase partitioning demonstrated that the 64-kDa protein is a hydrophilic polypeptide. These findings suggest that the 64-kDa protein is a soluble protein trapped in the space between the inner and outer envelope membranes. After sonication of mixed envelope membranes, the 64-kDa protein was no longer present in the membrane fraction, but could be found in the supernatant after a 110000 × g centrifugation

From the Bloch sphere to phase space representations with the Gottesman-Kitaev-Preskill encoding

In this work, we study the Wigner phase-space representation of qubit states encoded in continuous variables (CV) by using the Gottesman-Kitaev-Preskill (GKP) mapping. We explore a possible connection between resources for universal quantum computation in discrete-variable (DV) systems, i.e. non-stabilizer states, and negativity of the Wigner function in CV architectures, which is a necessary requirement for quantum advantage. In particular, we show that the lowest Wigner logarithmic negativity of qubit states encoded in CV with the GKP mapping corresponds to encoded stabilizer states, while the maximum negativity is associated with the most non-stabilizer states, H-type and T-type quantum states.Comment: (v1) Accepted for publication in the Springer's "Mathematics for Industry" series. (v2) Typo in the abstract fixed; URL of the conference where the paper has been presented added: International Symposium on Mathematics, Quantum Theory, and Cryptography (MQC), held in September 2019 in Fukuoka, Japan (https://www.mqc2019.org/mqc2019/program

Continuous-variable sampling from photon-added or photon-subtracted squeezed states

We introduce a new family of quantum circuits in Continuous Variables and we show that, relying on the widely accepted conjecture that the polynomial hierarchy of complexity classes does not collapse, their output probability distribution cannot be efficiently simulated by a classical computer. These circuits are composed of input photon-subtracted (or photon-added) squeezed states, passive linear optics evolution, and eight-port homodyne detection. We address the proof of hardness for the exact probability distribution of these quantum circuits by exploiting mappings onto different architectures of sub-universal quantum computers. We obtain both a worst-case and an average-case hardness result. Hardness of Boson Sampling with eight-port homodyne detection is obtained as the zero squeezing limit of our model. We conclude with a discussion on the relevance and interest of the present model in connection to experimental applications and classical simulations.Comment: 11 pages, 6 figure

Cloning and sequence analysis of cDNAs encoding the cytosolic precursors of subunits GapA and GapB of chloroplast glyceraldehyde-3-phosphate dehydrogenase from pea and spinach

Chloroplast glyceraldehyde-3-phosphate dehydrogenase (GAPDH) is composed of two different subunits, GapA and GapB. cDNA clones containing the entire coding sequences of the cytosolic precursors for GapA from pea and for GapB from pea and spinach have been identified, sequenced and the derived amino acid sequences have been compared to the corresponding sequences from tobacco, maize and mustard. These comparisons show that GapB differs from GapA in about 20% of its amino acid residues and by the presence of a flexible and negatively charged C-terminal extension, possibly responsible for the observed association of the enzyme with chloroplast envelopes in vitro. This C-terminal extension (29 or 30 residues) may be susceptible to proteolytic cleavage thereby leading to a conversion of chloroplast GAPDH isoenzyme I into isoenzyme II. Evolutionary rate comparisons at the amino acid sequence level show that chloroplast GapA and GapB evolve roughly two-fold slower than their cytosolic counterpart GapC. GapA and GapB transit peptides evolve about 10 times faster than the corresponding mature subunits. They are relatively long (68 and 83 residues for pea GapA and spinach GapB respectively) and share a similar amino acid framework with other chloroplast transit peptides

Seronegative patients vaccinated with cytomegalovirus gB-MF59 vaccine have evidence of neutralising antibody responses against gB early post-transplantation

Background Human cytomegalovirus (HCMV) causes a ubiquitous infection which can pose a significant threat for immunocompromised individuals, such as those undergoing solid organ transplant (SOT). Arguably, the most successful vaccine studied to date is the recombinant glycoprotein-B (gB) with MF59 adjuvant which, in 3 Phase II trials, demonstrated 43–50% efficacy in preventing HCMV acquisition in seronegative healthy women or adolescents and reduction in virological parameters after SOT. However, the mechanism of vaccine protection in seronegative recipients remains undefined. Methods We evaluated samples from the cohort of seronegative SOT patients enroled in the Phase II glycoprotein-B/MF59 vaccine trial who received organs from seropositive donors. Samples after SOT (0–90 days) were tested by real-time quantitative PCR for HCMV DNA. Anti-gB antibody levels were measured by ELISA. Neutralization was measured as a decrease in infectivity for fibroblast cell cultures revealed by expression of immediate-early antigens. Findings Serological analyses revealed a more rapid increase in the humoral response against gB post transplant in vaccine recipients than in those randomised to receive placebo. Importantly, a number of patient sera displayed HCMV neutralising responses – neutralisation which was abrogated by pre-absorbing the sera with recombinant gB. Interpretation We hypothesise that the vaccine primed the immune system of seronegative recipients which, when further challenged with virus at time of transplant, allowed the host to mount rapid immunological humoral responses even under conditions of T cell immune suppression during transplantation