Phases of Augmented Hadronic Light-Front Wave Functions

It is an important question whether the final/initial state gluonic interactions which lead to naive-time-reversal-odd single-spin asymmetries and diffraction at leading twist can be associated in a definite way with the light-front wave function hadronic eigensolutions of QCD. We use light-front time-ordered perturbation theory to obtain augmented light-front wave functions which contain an imaginary phase which depends on the choice of advanced or retarded boundary condition for the gauge potential in light-cone gauge. We apply this formalism to the wave functions of the valence Fock states of nucleons and pions, and show how this illuminates the factorization properties of naive-time-reversal-odd transverse momentum dependent observables which arise from rescattering. In particular, one calculates the identical leading-twist Sivers function from the overlap of augmented light-front wavefunctions that one obtains from explicit calculations of the single-spin asymmetry in semi-inclusive deep inelastic lepton-polarized nucleon scattering where the required phases come from the final-state rescattering of the struck quark with the nucleon spectators.Comment: 10 pages, 1 figur

Performance of Photosensors in the PandaX-I Experiment

We report the long term performance of the photosensors, 143 one-inch R8520-406 and 37 three-inch R11410-MOD photomultipliers from Hamamatsu, in the first phase of the PandaX dual-phase xenon dark matter experiment. This is the first time that a significant number of R11410 photomultiplier tubes were operated in liquid xenon for an extended period, providing important guidance to the future large xenon-based dark matter experiments.Comment: v3 as accepted by JINST with modifications based on reviewers' comment

Interaction of a symmetrical α,α',δ,δ'-Tetramethyl-cucurbit[6]uril with Ln³⁺ : potential applications for isolation of lanthanides

The interaction of a symmetrical α,α′,δ,δ′-tetramethyl-cucurbit[6]uril (TMeQ[6]) with a series of lanthanide cations (Ln³⁺) was investigated in neutral water and in acidic solution. Analysis by single crystal X-ray diffraction revealed that different isomorphous families formed under different synthetic conditions. Such differences in the interaction between TMeQ[6] and Ln³⁺ could potentially be used for isolating heavier Ln³⁺ from their lighter counterparts in neutral solution, and lighter lanthanide cations from their heavier counterparts in acidic solution

Mining Spatial-Temporal Patterns and Structural Sparsity for Human Motion Data Denoising

Motion capture is an important technique with a wide range of applications in areas such as computer vision, computer animation, film production, and medical rehabilitation. Even with the professional motion capture systems, the acquired raw data mostly contain inevitable noises and outliers. To denoise the data, numerous methods have been developed, while this problem still remains a challenge due to the high complexity of human motion and the diversity of real-life situations. In this paper, we propose a data-driven-based robust human motion denoising approach by mining the spatial-temporal patterns and the structural sparsity embedded in motion data. We first replace the regularly used entire pose model with a much fine-grained partlet model as feature representation to exploit the abundant local body part posture and movement similarities. Then, a robust dictionary learning algorithm is proposed to learn multiple compact and representative motion dictionaries from the training data in parallel. Finally, we reformulate the human motion denoising problem as a robust structured sparse coding problem in which both the noise distribution information and the temporal smoothness property of human motion have been jointly taken into account. Compared with several state-of-the-art motion denoising methods on both the synthetic and real noisy motion data, our method consistently yields better performance than its counterparts. The outputs of our approach are much more stable than that of the others. In addition, it is much easier to setup the training dataset of our method than that of the other data-driven-based methods

Mesoporous MgO promoted with NaNO3/NaNO2 for rapid and high-capacity CO2 capture at moderate temperatures

A series of mesoporous MgO samples with different morphologies were synthesized through a simple hydrothermal treatment and NaNO3/NaNO2 were used as promoters to enhance CO2 capture capacity at an intermediate temperature range (200–400 °C). The effects of hydrothermal solution pH and content of promoters were examined to determine the optimal synthesis conditions. The influence of operational temperatures, CO2 partial pressure, and performance over repeated cycles was investigated and the reaction mechanism was discussed. The mesoporous MgO promoted by NaNO3/NaNO2 exhibited a CO2 capture capacity as high as 19.8 mmol g−1 at 350 °C in the presence of 0.85 bar of CO2 within only 50 min. A “three-stage” reaction process was proposed based on a detailed sorption kinetics study, namely Stage I: initiating interactions between CO2 and exposed MgO; Stage II: generation and accumulation of Mg2+ and CO32−; and Stage III: fast carbonation. Gradual deterioration of sorbents was found over the first 5 cycles followed by stable regenerability in the 5−15th cycles. A kinetic study of the 15th cycle suggests that the deactivation of sorbents inhibited the accumulation of Mg2+ and CO32− in Stage II and suppressed the carbonation in Stage III. A range of characterizations were undertaken revealing the morphology and structure of both fresh and regenerated sorbents. The results confirmed that, other than the sintering effect due to phase transition, the transformation of MgO skeleton is also an important contributor to the gradual deactivation of the sorbents over the first 5 cycles. More severe sintering effect under harsh decarbonation conditions suppressed the stability of the sorbents over cycles

Tim-3 Negatively Regulates IL-12 Expression by Monocytes in HCV Infection

T cell immunoglobulin and mucin domain-containing protein 3 (Tim-3) is a newly identified negative immunomodulator that is up-regulated on dysfunctional T cells during viral infections. The expression and function of Tim-3 on human innate immune responses during HCV infection, however, remains poorly characterized. In this study, we report that Tim-3 is constitutively expressed on human resting CD14+ monocyte/macrophages (M/MØ) and functions as a cap to block IL-12, a key pro-inflammatory cytokine linking innate and adaptive immune responses. Tim-3 expression is significantly reduced and IL-12 expression increased upon stimulation with Toll-like receptor 4 (TLR4) ligand - lipopolysaccharide (LPS) and TLR7/8 ligand - R848. Notably, Tim-3 is over-expressed on un-stimulated as well as TLR-stimulated M/MØ, which is inversely associated with the diminished IL-12 expression in chronically HCV-infected individuals when compared to healthy subjects. Up-regulation of Tim-3 and inhibition of IL-12 are also observed in M/MØ incubated with HCV-expressing hepatocytes, as well as in primary M/MØ or monocytic THP-1 cells incubated with HCV core protein, an effect that mimics the function of complement C1q and is reversible by blocking the HCV core/gC1qR interaction. Importantly, blockade of Tim-3 signaling significantly rescues HCV-mediated inhibition of IL-12, which is primarily expressed by Tim-3 negative M/MØ. Tim-3 blockade reduces HCV core-mediated expression of the negative immunoregulators PD-1 and SOCS-1 and increases STAT-1 phosphorylation. Conversely, blocking PD-1 or silencing SOCS-1 gene expression also decreases Tim-3 expression and enhances IL-12 secretion and STAT-1 phosphorylation. These findings suggest that Tim-3 plays a crucial role in negative regulation of innate immune responses, through crosstalk with PD-1 and SOCS-1 and limiting STAT-1 phosphorylation, and may be a novel target for immunotherapy to HCV infection

TiSGeD: a database for tissue-specific genes

Summary: The tissue-specific genes are a group of genes whose function and expression are preferred in one or several tissues/cell types. Identification of these genes helps better understanding of tissue–gene relationship, etiology and discovery of novel tissue-specific drug targets. In this study, a statistical method is introduced to detect tissue-specific genes from more than 123 125 gene expression profiles over 107 human tissues, 67 mouse tissues and 30 rat tissues. As a result, a novel subject-specialized repository, namely the tissue-specific genes database (TiSGeD), is developed to represent the analyzed results. Auxiliary information of tissue-specific genes was also collected from biomedical literatures

New Spinor Field Realizations of the Non-Critical W3W_{3} String

We investigate the new spinor field realizations of the $W_{3}$ algebra, making use of the fact that the $W_{3}$ algebra can be linearized by the addition of a spin-1 current. We then use these new realizations to build the nilpotent Becchi-Rouet-Stora--Tyutin (BRST) charges of the spinor non-critical $W_{3}$ string.Comment: 8 pages, no figures, revtex4 style, accepted by Chin. Phys. Let