An enhanced brain storm sine cosine algorithm for global optimization problems

The conventional sine cosine algorithm (SCA) does not appropriately balance exploration and exploitation, causing premature convergence, especially for complex optimization problems, such as the complex shifted or shifted rotated problems. To address this issue, this paper proposes an enhanced brain storm SCA (EBS-SCA), where an EBS strategy is employed to improve the population diversity, and by combining it with two different update equations, two new individual update strategies [individual update strategies (IUS): IUS-I and IUS-II] are developed to make effective balance between exploration and exploitation during the entire iterative search process. Double sets of benchmark suites involving 46 popular functions and two real-world problems are employed to compare the EBS-SCA with other metaheuristic algorithms. The experimental results validate that the proposed EBS-SCA achieves the overall best performance including the global search ability, convergence speed, and scalability

A Vector Grouping Learning Brain Storm Optimization Algorithm for Global Optimization Problems

The original brain storm optimization (BSO) method does not rationally compromise global exploration and local exploitation capability, which results in the premature convergence when solving complicated optimization problems like the shifted or shifted rotated functions. To address this problem, the paper develops a vector grouping learning BSO (VGLBSO) method. In VGLBSO, the individuals’ creation based on vector grouping learning (IC-VGL) scheme is first developed to improve the population diversity and compromise the global exploration and local exploitation capability. Moreover, a hybrid individuals’ update (H-IU) scheme is established by reasonably combing two different individuals’ update schemes, which further compromises the global exploration and local exploitation capability. Finally, the random grouping (RG) scheme, instead of K-means grouping is allowed to shrink the computational cost and maintain the diversity of the information exchange between different individuals. Twenty-eight popular benchmark functions are used to compare VGLBSO with 12 BSO and nine swarm intelligence methods. Experimental results present that VGLBSO achieves the best overall performance including the global search ability, convergence speed, and scalability amongst all the compared algorithms

Correlation property of length sequences based on global structure of complete genome

This paper considers three kinds of length sequences of the complete genome. Detrended fluctuation analysis, spectral analysis, and the mean distance spanned within time $L$ are used to discuss the correlation property of these sequences. The values of the exponents from these methods of these three kinds of length sequences of bacteria indicate that the long-range correlations exist in most of these sequences. The correlation have a rich variety of behaviours including the presence of anti-correlations. Further more, using the exponent $\gamma$, it is found that these correlations are all linear ($\gamma=1.0\pm 0.03$). It is also found that these sequences exhibit $1/f$ noise in some interval of frequency ($f>1$). The length of this interval of frequency depends on the length of the sequence. The shape of the periodogram in $f>1$ exhibits some periodicity. The period seems to depend on the length and the complexity of the length sequence.Comment: RevTex, 9 pages with 5 figures and 3 tables. Phys. Rev. E Jan. 1,2001 (to appear

A Catalog of Luminous Infrared Galaxies in the IRAS Survey and the Second Data Release of the SDSS

We select the Luminous Infrared Galaxies by cross-correlating the Faint Source Catalogue (FSC) and Point Source Catalogue (PSC) of the IRAS Survey with the Second Data Release of the SDSS for studying their infrared and optical properties. The total number of our sample is 1267 for FSC and 427 for PSC by using 2$\sigma$ significance level cross-section. The "likelihood ratio" method is used to estimate the sample's reliability and for a more reliable subsample (908 for FSC and 356 for PSC) selection. Then a Catalog with both the infrared, optical and radio informations is presented and will be used in further works. Some statistical results show that the Luminous Infrared Galaxies are quite different from the Ultra-Luminous Infrared Galaxies. The AGN fractions of galaxies with different infrared luminosities and the radio to infrared correlations are consist with previous studies.Comment: 15 pages, 11 figures. Accepted by ChJAA. Reference adde

Multiple Nodeless Superconducting Gaps in (Ba0.6K0.4)Fe2As2 Superconductor from Angle-Resolved Photoemission Spectroscopy

High resolution angle-resolved photoemission measurements have been carried out to study the superconducting gap in the (Ba0.6K0.4)Fe2As2 superconductor with Tc=35 K. Two hole-like Fermi surface sheets around the G(0,0) point exhibit different superconducting gaps. The inner Fermi surface sheet shows larger (10-12 meV) and slightly momentum-dependent gap while the outer one has smaller (7-8 meV) and nearly isotropic gap. The lack of gap node in both Fermi surface sheets favours s-wave superconducting gap symmetry. Superconducting gap opening is also observed at the M(pi,pi) point. The two Fermi surface spots near the M point are gapped below Tc but the gap persists above Tc. The rich and detailed superconducting gap information will provide key insights and constraints in understanding pairing mechanism in the iron-based superconductors.Comment: 11 pages, 4 figure

A New Look at the Scalar Meson f0(500)f_0(500) via D+→π+π−ℓ+νℓD^+\to \pi^+\pi^-\ell^+\nu_\ell Decays

Using $2.93~\mathrm{fb}^{-1}$ of $e^+e^-$ collision data collected with the BESIII detector at the center-of-mass energy of 3.773 GeV, we investigate the semileptonic decays $D^+\to \pi^+\pi^- \ell^+\nu_\ell$ ($\ell=e$ and $\mu$). The $D^+\to f_0(500)\mu^+\nu_\mu$ decay is observed for the first time. By analyzing simultaneously the differential decay rates of $D^+\to f_0(500) \mu^+\nu_\mu$ and $D^+\to f_0(500) e^+\nu_e$ in different $\ell^+\nu_\ell$ four-momentum transfer intervals, the product of the relevant hadronic form factor $f^{f_0}_{+}(0)$ and the magnitude of the $c\to d$ Cabibbo-Kobayashi-Maskawa matrix element $|V_{cd}|$ is determined to be $f_{+}^{f_0} (0)|V_{cd}|=0.0787\pm0.0060_{\rm stat}\pm0.0033_{\rm syst}$ for the first time. With the input of $|V_{cd}|$ from the global fit in the standard model, we determine $f_{+}^{f_0} (0)=0.350\pm0.027_{\rm stat}\pm0.015_{\rm syst}$. The absolute branching fractions of $D^+\to f_0(500)_{(\pi^+\pi^-)}\mu^+\nu_\mu$ and $D^+\to \rho^0_{(\pi^+\pi^-)} \mu^+\nu_\mu$ are determined as $(0.72\pm0.13_{\rm stat}\pm0.10_{\rm syst})\times10^{-3}$ and $(1.64\pm0.13_{\rm stat}\pm0.11_{\rm syst})\times 10^{-3}$. Combining these results with those of previous BESIII measurements on their semielectronic counterparts from the same data sample, we test lepton flavor universality by measuring the branching fraction ratios ${\mathcal B}_{D^+\to \rho^0 \mu^+\nu_\mu}/{\mathcal B}_{D^+\to \rho^0 e^+\nu_e}=0.88\pm0.10$ and ${\mathcal B}_{D^+\to f_0(500) \mu^+\nu_\mu}/{\mathcal B}_{D^+\to f_0(500) e^+\nu_e}=1.14\pm0.28$, which are compatible with the standard model expectation.Comment: Supplemental Materials added in this versio

Tissue microarray analysis reveals a tight correlation between protein expression pattern and progression of esophageal squamous cell carcinoma

BACKGROUND: The development of esophageal squamous cell carcinoma (ESCC) progresses a multistage process, collectively known as precursor lesions, also called dysplasia (DYS) and carcinoma in situ (CIS), subsequent invasive lesions and final metastasis. In this study, we are interested in investigating the expression of a variety of functional classes of proteins in ESCC and its precursor lesions and characterizing the correlation of these proteins with ESCC malignant progression. METHODS: Fas, FADD, caspase 8, CDC25B, fascin, CK14, CK4, annexin I, laminin-5γ2 and SPARC were analyzed using immunohistochemistry on tissue microarray containing 205 ESCC and 173 adjacent precursor lesions as well as corresponding normal mucosa. To confirm the immunohistochemical results, three proteins, fascin, CK14 and laminin-5γ2, which were overexpressed in ESCC on tissue microarray, were detected in 12 ESCC cell lines by Western blot assay. RESULTS: In ESCC and its precursor lesions, FADD, CDC25B, fascin, CK14, laminin-5γ2 and SPARC were overexpressed, while Fas, caspase 8, CK4 and annexin I were underexpressed. The abnormalities of these proteins could be classified into different groups in relation to the stages of ESCC development. They were "early" corresponding to mild and moderate DYS with overexpression of fascin, FADD and CDC25B and underexpression of Fas, caspase 8, CK4 and annexin I, "intermediate" to severe DYS and CIS with overexpression of FADD and CK14, and "late" to invasive lesions (ESCC) and to advanced pTNM stage ESCC lesions with overexpression of CK14, laminin-5γ2 and SPARC. CONCLUSION: Analyzing the protein expression patterns of Fas, FADD, caspase 8, CDC25B, fascin, CK14, CK4, annexin I, laminin-5γ2 and SPARC would be valuable to develop rational strategies for early detection of lesions at risk in advance as well as for prevention and treatment of ESCC

Observation of the decay hc→3(π+π−)π0h_{c}\to3(\pi^{+}\pi^{-})\pi^{0}

Based on $(2712.4\pm14.1)\times10^{6}$ $\psi(3686)$ events collected with the BESIII detector, we study the decays $h_{c}\to3(\pi^{+}\pi^{-})\pi^{0}$, $h_{c}\to2(\pi^{+}\pi^{-})\omega$, $h_{c}\to2(\pi^{+}\pi^{-})\pi^{0}\eta$, $h_{c}\to2(\pi^{+}\pi^{-})\eta$, and $h_{c}\to p\bar{p}$ via $\psi(3686)\to\pi^{0}h_{c}$. The decay channel $h_{c}\to3(\pi^{+}\pi^{-})\pi^{0}$ is observed for the first time, and its branching fraction is determined to be $\left( {9.28\pm 1.14 \pm 0.77} \right) \times {10^{ - 3}}$, where the first uncertainty is statistical and the second is systematic. In addition, first evidence is found for the modes $h_{c} \to 2(\pi^{+}\pi^{-})\pi^{0}\eta$ and $h_{c}\to2(\pi^{+}\pi^{-})\omega$ with significances of 4.8$\sigma$ and 4.7$\sigma$, and their branching fractions are determined to be $(7.55\pm1.51\pm0.77)\times10^{-3}$ and $\left( {4.00 \pm 0.86 \pm 0.35}\right) \times {10^{ - 3}}$, respectively. No significant signals of $h_c\to 2(\pi^+\pi^-)\eta$ and $h_{c}\to p\bar{p}$ are observed, and the upper limits of the branching fractions of these decays are determined to be $<6.19\times10^{-4}$ and $<4.40\times10^{-5}$ at the 90% confidence level, respectively.Comment: 11 pages, 3 figure

Composition, Diversity, and Origin of the Bacterial Community in Grass Carp Intestine

Gut microbiota has become an integral component of the host, and received increasing attention. However, for many domestic animals, information on the microbiota is insufficient and more effort should be exerted to manage the gastrointestinal bacterial community. Understanding the factors that influence the composition of microbial community in the host alimentary canal is essential to manage or improve the microbial community composition. In the present study, 16S rRNA gene sequence-based comparisons of the bacterial communities in the grass carp (Ctenopharyngodon idellus) intestinal contents and fish culture-associated environments are performed. The results show that the fish intestinal microbiota harbors many cellulose-decomposing bacteria, including sequences related to Anoxybacillus, Leuconostoc, Clostridium, Actinomyces, and Citrobacter. The most abundant bacterial operational taxonomic units (OTUs) in the grass carp intestinal content are those related to feed digestion. In addition, the potential pathogens and probiotics are important members of the intestinal microbiota. Further analyses show that grass carp intestine holds a core microbiota composed of Proteobacteria, Firmicutes, and Actinobacteria. The comparison analyses reveal that the bacterial community in the intestinal contents is most similar to those from the culture water and sediment. However, feed also plays significant influence on the composition of gut microbiota

First Measurement of the Decay Asymmetry in the pure W-boson-exchange Decay Λc+→Ξ0K+\Lambda_{c}^{+}\to\Xi^{0}K^{+}

Based on $4.4~\text{fb}^{-1}$ of $e^{+}e^{-}$ annihilation data collected at the center-of-mass energies between $4.60$ and $4.70~\text{GeV}$ with the BESIII detector at the BEPCII collider, the pure \textit{W}-boson-exchange decay $\Lambda_{c}^{+}\to\Xi^{0}K^{+}$ is studied with a full angular analysis. The corresponding decay asymmetry is measured for the first time to be $\alpha_{\Xi^{0}K^{+}}=0.01\pm0.16({\rm stat.})\pm0.03({\rm syst.})$. This result reflects the non-interference effect between the $S$- and $P$-wave amplitudes. The phase shift between $S$- and $P$-wave amplitudes has two solutions, which are $\delta_{p}-\delta_{s}=-1.55\pm0.25({\rm stat.})\pm0.05({\rm syst.})~\text{rad}$ or $1.59\pm0.25({\rm stat.})\pm0.05({\rm syst.})~\text{rad}$