Proto-clusters in the Lambda CDM Universe

We compare the highly clustered populations of very high redshift galaxies with proto-clusters identified numerically in a standard $\Lambda$CDM universe ($\Omega_0=0.3, \lambda_0=0.7$) simulation. We evolve 256^3 dark matter particles in a comoving box of side 150h^{-1}Mpc. By the present day there are 63 cluster sized objects of mass in excess of 10^{14}h^{-1}Mo in this box. We trace these clusters back to higher redshift finding that their progenitors at z=4--5 are extended regions of typically 20--40 Mpc (comoving) in size, with dark halos of mass in excess of 10^{12}h^{-1}Mo and are overdense by typically 1.3--13 times the cosmological mean density. Comparison with the observation of Lyman alpha emitting (LAEs) galaxies at z=4.86 and at z=4.1 indicates that the observed excess clustering is consistent with that expected for a proto-cluster region if LAEs typically correspond to massive dark halos of more than 10^{12}h^{-1}Mo. We give a brief discussion on the relation between high redshift concentration of massive dark halos and present day rich clusters of galaxies.Comment: 4 pages, 5 figures, Accepted for publication in ApJ Letter

Perfect State Transfer in Laplacian Quantum Walk

For a graph $G$ and a related symmetric matrix $M$, the continuous-time quantum walk on $G$ relative to $M$ is defined as the unitary matrix $U(t) = \exp(-itM)$, where $t$ varies over the reals. Perfect state transfer occurs between vertices $u$ and $v$ at time $\tau$ if the $(u,v)$-entry of $U(\tau)$ has unit magnitude. This paper studies quantum walks relative to graph Laplacians. Some main observations include the following closure properties for perfect state transfer: (1) If a $n$-vertex graph has perfect state transfer at time $\tau$ relative to the Laplacian, then so does its complement if $n\tau$ is an integer multiple of $2\pi$. As a corollary, the double cone over any $m$-vertex graph has perfect state transfer relative to the Laplacian if and only if $m \equiv 2 \pmod{4}$. This was previously known for a double cone over a clique (S. Bose, A. Casaccino, S. Mancini, S. Severini, Int. J. Quant. Inf., 7:11, 2009). (2) If a graph $G$ has perfect state transfer at time $\tau$ relative to the normalized Laplacian, then so does the weak product $G \times H$ if for any normalized Laplacian eigenvalues $\lambda$ of $G$ and $\mu$ of $H$, we have $\mu(\lambda-1)\tau$ is an integer multiple of $2\pi$. As a corollary, a weak product of $P_{3}$ with an even clique or an odd cube has perfect state transfer relative to the normalized Laplacian. It was known earlier that a weak product of a circulant with odd integer eigenvalues and an even cube or a Cartesian power of $P_{3}$ has perfect state transfer relative to the adjacency matrix. As for negative results, no path with four vertices or more has antipodal perfect state transfer relative to the normalized Laplacian. This almost matches the state of affairs under the adjacency matrix (C. Godsil, Discrete Math., 312:1, 2011).Comment: 26 pages, 5 figures, 1 tabl

Effect of Multi- Steel Bolt Anchorages on Composite Beams

Using fiber-reinforced polymer (FRP) to retrofit or strengthen the concrete structures is an attractive option in construction areas nowadays. However, premature debonding failures limit the efficacy of fiber utilization. It is presently accepted that anchorage system is an attractive option to solve this problem. Much efforts has been made through experimental testing and numerical modeling to investigate the anchorage systems, meanwhile various systems were created and developed. However, researches on the mechanism of the anchorage systems are still too rare to build a countable and union design guideline with respect to different premature debonding failure modes. The present paper focused on two commonly documented anchorage methods: steel bolt anchorage and CFRP end wrapping anchorage and conducted a specially design experiment to further analyze the mechanism of effect of both systems on premature debonding failures (concrete cover separation and IC debonding). Results show that CFRP wrapping and Steel bolts can both effectively stop or suppress the propagation of IC debonding. And the ultimate load is effected by the finally failure mode, which could be changed with different height of steel bolt

GLIDA: GPCR—ligand database for chemical genomics drug discovery—database and tools update

G-protein coupled receptors (GPCRs) represent one of the most important families of drug targets in pharmaceutical development. GLIDA is a public GPCR-related Chemical Genomics database that is primarily focused on the integration of information between GPCRs and their ligands. It provides interaction data between GPCRs and their ligands, along with chemical information on the ligands, as well as biological information regarding GPCRs. These data are connected with each other in a relational database, allowing users in the field of Chemical Genomics research to easily retrieve such information from either biological or chemical starting points. GLIDA includes a variety of similarity search functions for the GPCRs and for their ligands. Thus, GLIDA can provide correlation maps linking the searched homologous GPCRs (or ligands) with their ligands (or GPCRs). By analyzing the correlation patterns between GPCRs and ligands, we can gain more detailed knowledge about their conserved molecular recognition patterns and improve drug design efforts by focusing on inferred candidates for GPCR-specific drugs. This article provides a summary of the GLIDA database and user facilities, and describes recent improvements to database design, data contents, ligand classification programs, similarity search options and graphical interfaces. GLIDA is publicly available at http://pharminfo.pharm.kyoto-u.ac.jp/services/glida/. We hope that it will prove very useful for Chemical Genomics research and GPCR-related drug discovery

BoostingTree: parallel selection of weak learners in boosting, with application to ranking

Boosting algorithms have been found successful in many areas of machine learning and, in particular, in ranking. For typical classes of weak learners used in boosting (such as decision stumps or trees), a large feature space can slow down the training, while a long sequence of weak hypotheses combined by boosting can result in a computationally expensive model. In this paper we propose a strategy that builds several sequences of weak hypotheses in parallel, and extends the ones that are likely to yield a good model. The weak hypothesis sequences are arranged in a boosting tree, and new weak hypotheses are added to promising nodes (both leaves and inner nodes) of the tree using some randomized method. Theoretical results show that the proposed algorithm asymptotically achieves the performance of the base boosting algorithm applied. Experiments are provided in ranking web documents and move ordering in chess, and the results indicate that the new strategy yields better performance when the length of the sequence is limited, and converges to similar performance as the original boosting algorithms otherwise. © 2013 The Author(s)

Constitutional Flavonoids Derived from Epimedium Dose-Dependently Reduce Incidence of Steroid-Associated Osteonecrosis Not via Direct Action by Themselves on Potential Cellular Targets

Intravascular-thrombosis and extravascular-lipid-deposit are the two key pathogenic events considered to interrupt intraosseous blood supply during development of steroid-associated osteonecrosis (ON). However, there are no clinically employed agents capable of simultaneously targeting these two key pathogenic events. The present experimental study demonstrated that constitutional flavonoid glycosides derived from herb Epimedium (EF, composed of seven flavonoid compounds with common stem nuclear) exerted dose-dependent effect on inhibition of both thrombosis and lipid-deposition and accordingly reducing incidence of steroid-associated ON in rabbits, which was not via direct action by themselves rather by their common metabolite on potential cellular targets involved in the two pathogenic pathways. The underlying mechanism could be explained by counteracting endothelium injury and excessive adipogenesis. These findings encourage designing clinical trials to investigate potential of EF in prevention of steroid-associated ON