701 research outputs found

    Fish play Minority Game as humans do

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    Previous computer simulations of the Minority Game (MG) have shown that the average agent number in the winning group (i.e., the minority group) had a maximal value such that the global gain was also maximal when an optimal amount of information was available to all agents . This property was further examined and its connection to financial markets has also been discussed . Here we report the results of an unprecedented real MG played by university staff members who clicked one of two identical buttons (A and B) on a computer screen while clocking in or out of work. We recorded the number of people who clicked button A for 1288 games, beginning on April 21, 2008 and ending on October 31, 2010, and calculated the variance among the people who clicked A as a function of time. We find that variance per person decreases to a minimum and rises to a value close to 1/4 which is the expected value when agents click buttons randomly. Our results are consistent with previous simulation results for the theoretical MG and suggest that our agents had employed more information for their strategies as their experience playing the game grew. We also carried out another experiment in which we forced 101 fish to enter one of the two symmetric chambers (A and B). We repeated the fish experiment 500 times and found that the variance of the number of fish that entered chamber A also decreased to a minimum and then increased to a saturated value, suggesting that fish have memory and can employ more strategies when facing the same situation again and again

    Linking emergent phenomena and broken symmetries through one-dimensional objects and their dot/cross products

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    The symmetry of the whole experimental setups, including specific sample environments and measurables, can be compared with that of specimens for observable physical phenomena. We, first, focus on one-dimensional (1D) experimental setups, independent from any spatial rotation around one direction, and show that eight kinds of 1D objects (four; vectorlike, the other four; director-like), defined in terms of symmetry, and their dot and cross products are an effective way for the symmetry consideration. The dot products form a Z2xZ2xZ2 group with Abelian additive operation, and the cross products form a Z2xZ2 group with Abelian additive operation or Q8, a non-abelian group of order eight, depending on their signs. Those 1D objects are associated with characteristic physical phenomena. When a 3D specimen has Symmetry Operational Similarity (SOS) with (identical or lower, but not higher, symmetries than) an 1D object with a particular phenomenon, the 3D specimen can exhibit the phenomenon. This SOS approach can be a transformative and unconventional avenue for symmetry-guided materials designs and discoveries.Comment: 12 pages, 6 figure

    Higher-order QCD corrections to Ξ₯\Upsilon decay into double charmonia

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    In this work, we study the exclusive decay of Ξ₯\Upsilon into J/ψJ/\psi in association with Ξ·c\eta_c (Ο‡c0,1,2\chi_{c0,1,2}). The decay widths for different helicity configurations are evaluated up to QCD next-to-leading order within the nonrelativistic QCD framework. We find that the QCD corrections notably mitigate the renormalization scale dependence of the decay widths for all the processes. The branching fraction of Ξ₯β†’J/ψ+Ο‡c1\Upsilon\rightarrow J/\psi+\chi_{c1} is obtained as 3.73βˆ’2.06βˆ’1.19+5.10+0.10Γ—10βˆ’63.73^{+5.10+0.10}_{-2.06-1.19}\times 10^{-6}, which agrees well with the Belle measurement, i.e., Br(Ξ₯β†’J/ψ+Ο‡c1)=(3.90Β±1.21Β±0.23)Γ—10βˆ’6{\rm Br}(\Upsilon\rightarrow J/\psi+\chi_{c1})=(3.90\pm1.21\pm0.23)\times10^{-6}. For the other processes, our results of the branching fractions are compatible with the upper limits given by the Belle experiments, except for Ξ₯(2S)β†’J/ψ+Ο‡c1\Upsilon(2S)\to J/\psi +\chi_{c1}, where some tension exists between theory and experiment. Having the polarized decay widths, we study the J/ψJ/\psi polarization, which turn out to be independent of any nonperturbative parameters. Further, according to our calculation, it is promising to measure all the processes at Super B factory thanks to the high luminosity.Comment: 13 pages, 2 figures, 3 tables, to match the version accepted for publication in PR

    Haplotype Distribution and Evolutionary Pattern of miR-17 and miR-124 Families Based on Population Analysis

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    Background: MicroRNAs (miRNAs) are small, endogenously expressed non-coding RNAs that regulate mRNAs posttranscriptionally. Previous studies have explored miRNA evolutionary trend, but evolutionary history and pattern in the miRNA world are still not fully clear. In the paper, we intended to analyze miRNA haplotype distribution and evolutionary network by analyzing miRNA sequences of miR-17 and miR-124 families across animal species as special populations. Principal Findings: 31 haplotypes were detected in miR-17 family while only 9 haplotypes were defined in miR-124 family. The complex miR-17 family was mainly distributed in vertebrates, but miR-124 was shared by more animal species from Caenorhabditis to Homo and had a wide distribution spectrum. Some haplotypes of the two miRNA families appeared discontinuous distributions across animals. Compared with a simple phylogenetic network in miR-124 family, miR-17 family indicated a complex network with some median vectors that might be lost ancestral or potential miRNA haplotypes. By analyzing different miRNAs across 12 animal species, we found these small RNAs showed different haplotype diversities, haplotype distributions and phylogenetic networks. Conclusions: Different miRNAs had quite different haplotype distributions and evolutionary patterns. Discontinuous distributions of miRNAs and median vectors in phylogenetic networks implied more members in the miRNA world. miRN
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