Entanglement criterion via general symmetric informationally complete measurements

We study the quantum separability problem by using general symmetric informationally complete measurements and present a separability criterion for arbitrary dimensional bipartite systems. We show by detailed examples that our criterion is more powerful than the existing ones in entanglement detection.Comment: 8 pages, 5 figure

Detecting EPR steering via two classes of local measurements

We study the Einstein-Podolsky-Rosen (EPR) steering and present steerability criteria for arbitrary qubit-qudit (qudit-qubit) systems based on mutually unbiased measurements (MUMs) and general symmetric informationally complete measurements (general SIC-POVMs). Avoiding the usual complicated steering inequalities, these criteria can be more operational than some existing criteria and implemented experimentally. Detailed examples are given to illustrate the efficiency of the criteria in both computation and experimental implementation.Comment: 8 pages, 1 figur

Discriminating bipartite mixed states by local operations

Unambiguous state discrimination of two mixed bipartite states via local operations and classical communications (LOCC) is studied and compared with the result of a scheme realized via global measurement. We show that the success probability of a global scheme for mixed-state discrimination can be achieved perfectly by the local scheme. In addition, we simulate this discrimination via a pair of pure entangled bipartite states. This simulation is perfect for local rather than global schemes due to the existence of entanglement and global coherence in the pure states. We also prove that LOCC protocol and the sequential state discrimination (SSD) can be interpreted in a unified view. We then hybridize the LOCC protocol with three protocols (SSD, reproducing and broadcasting) relying on classical communications. Such hybridizations extend the gaps between the optimal success probability of global and local schemes, which can be eliminated only for the SSD rather than the other two protocols

Hydrothermal synthesis and crystal structure of Na2In2[PO3(OH)]4·H2O with a new structure type

A sodium indium hydrogen phosphate hydrate, Na2In2[PO3 (OH)](4).H2O, was synthesized under mild hydrothermal conditions, and the crystal structure was characterized by the single-crystal X-ray diffraction method. The structure is of a new type with the following data: Mr = 794.775, triclinic, aP62, P-1 (No. 2), a = 9.3013(1) Angstrom, b = 9.4976(1) Angstrom, c = 9.2685(7) Angstrom, alpha = 98.710(4)degrees, beta = 98.953(4)degrees gamma = 60.228(6)degrees V = 699.42(5) Angstrom (3), Z = 2, D-x = 3.217 g cm(-3), lambda = 0.71073 Angstrom, mu = 39.1 cm(-1), F(000) = 644, T = 293 K, R = 0.0551, wR = 0.1528 for 245 variables and 4559 contributing unique reflections. The structure is characterized by corner-sharing InO6 and PO4H polyhedra forming a three-dimensional network with infinite channels along the [100] direction, where sodium cations and water molecules reside through hydrogen bonds. The topological construction of the title structure can be considered closely related to an augmented corundum network and the augmentation of the 4, 6 net has largely increased the porosity of the compound. The thermal stability investigation shows that the compound loses its water molecules around 365 degreesC and is nonzeolitic in character. (C) 2001 Academic Press

XPD codon 312 and 751 polymorphisms, and AFB1 exposure, and hepatocellular carcinoma risk

<p>Abstract</p> <p>Background</p> <p>Genetic polymorphisms in DNA repair genes may influence individual variation in DNA repair capacity, which may be associated with risk of hepatocellular carcinoma (HCC) related to the exposure of aflatoxin B1 (AFB1). In this study, we have focused on the polymorphisms of xeroderma pigmentosum complementation group D (XPD) codon 312 and 751 (namely Asp312Asn and Lys751Gln), involved in nucleotide excision repair.</p> <p>Methods</p> <p>We conducted a case-control study including 618 HCC cases and 712 controls to evaluate the associations between these two polymorphisms and HCC risk for Guangxi population by means of TaqMan-PCR and PCR-RFLP analysis.</p> <p>Results</p> <p>We found that individuals featuring the XPD genotypes with codon 751 Gln alleles (namely XPD-LG or XPD-GG) were related to an elevated risk of HCC compared to those with the homozygote of XPD codon 751 Lys alleles [namely XPD-LL, adjusted odds ratios (ORs) were 1.75 and 2.47; 95% confidence interval (CIs) were 1.30-2.37 and 1.62-3.76, respectively]. A gender-specific role was evident that showed an higher risk for women (adjusted OR was 8.58 for XPD-GG) than for men (adjusted OR = 2.90 for XPD-GG). Interestingly, the interactive effects of this polymorphism and AFB1-exposure information showed the codon 751 Gln alleles increase the risk of HCC for individuals facing longer exposure years (<it>P</it>_interaction= 0.011, OR = 0.85). For example, long-exposure-years (> 48 years) individuals who carried XDP-GG had an adjusted OR of 470.25, whereas long-exposure-years people with XDP-LL were at lower risk (adjusted OR = 149.12). However, we did not find that XPD codon 312 polymorphism was significantly associated with HCC risk.</p> <p>Conclusion</p> <p>These findings suggest that XPD Lys751Gln polymorphism is an important modulator of AFB1 related-HCC development in Guangxi population.</p

Methodology and applications of city level CO2 emission accounts in China

China is the world's largest energy consumer and CO2 emitter. Cities contribute 85% of the total CO2 emissions in China and thus are considered as the key areas for implementing policies designed for climate change adaption and CO2 emission mitigation. However, the emission inventory construction of Chinese cities has not been well researched, mainly owing to the lack of systematic statistics and poor data quality. Focusing on this research gap, we developed a set of methods for constructing CO2 emissions inventories for Chinese cities based on energy balance table. The newly constructed emission inventory is compiled in terms of the definition provided by the IPCC territorial emission accounting approach and covers 47 socioeconomic sectors, 17 fossil fuels and 9 primary industry products, which is corresponding with the national and provincial inventory. In the study, we applied the methods to compile CO2 emissions inventories for 24 common Chinese cities and examined uncertainties of the inventories. Understanding the emissions sources in Chinese cities is the basis for many climate policy and goal research in the future

DPHL: A DIA Pan-human Protein Mass Spectrometry Library for Robust Biomarker Discovery

To address the increasing need for detecting and validating protein biomarkers in clinical specimens, mass spectrometry (MS)-based targeted proteomic techniques, including the selected reaction monitoring (SRM), parallel reaction monitoring (PRM), and massively parallel data-independent acquisition (DIA), have been developed. For optimal performance, they require the fragment ion spectra of targeted peptides as prior knowledge. In this report, we describe a MS pipeline and spectral resource to support targeted proteomics studies for human tissue samples. To build the spectral resource, we integrated common open-source MS computational tools to assemble a freely accessible computational workflow based on Docker. We then applied the workflow to generate DPHL, a comprehensive DIA pan-human library, from 1096 data-dependent acquisition (DDA) MS raw files for 16 types of cancer samples. This extensive spectral resource was then applied to a proteomic study of 17 prostate cancer (PCa) patients. Thereafter, PRM validation was applied to a larger study of 57 PCa patients and the differential expression of three proteins in prostate tumor was validated. As a second application, the DPHL spectral resource was applied to a study consisting of plasma samples from 19 diffuse large B cell lymphoma (DLBCL) patients and 18 healthy control subjects. Differentially expressed proteins between DLBCL patients and healthy control subjects were detected by DIA-MS and confirmed by PRM. These data demonstrate that the DPHL supports DIA and PRM MS pipelines for robust protein biomarker discovery. DPHL is freely accessible at https://www.iprox.org/page/project.html?id=IPX0001400000

Improved Measurement of Electron Antineutrino Disappearance at Daya Bay

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