2,115 research outputs found

    Wandering globular clusters: the first dwarf galaxies in the universe?

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    In the last decade we witness an advent of new types of dwarf stellar systems in cluding ultra-compact dwarfs, ultra-faint dwarf spheroidals, and exotic globular clusters, breaking the old simple paradigm for dwarf galaxies and globular clusters. These objects become more intriguing, and understanding of these new findings be comes more challenging. Recently we discovered a new type of large scale structure in the Virgo cluster of galaxies: it is composed of globular clusters. Globular clusters in Virgo are found wandering between galaxies (intracluster globular clusters) as well as in galaxies. These intracluster globular clusters fill a significant fraction in the area of the Virgo cluster and they are dominated by blue globular clusters. These intracluster globular clusters may be closely related with the first dwarf galaxies in the universe.Comment: 6 pages, 3 figures, Conference Proceedings: "A Universe of Dwarf Galaxies", 14-18 June 2010, Lyon, Franc

    UBV stellar photometry of bright stars in GC M5. I. UV colour-magnitude and colour-colour diagrams and some peculiarities in the HB stellar distribution

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    We present stellar photometry in the UBV passbands for the globular cluster M5 = NGC5904. The observations, short-exposured photographic plates and CCD frames, were obtained in the RC-focus of the 2m telescope of the Natl. Astron. Obs. 'Rozhen'. All stars in an annulus with radius 1 < r < 5.5 arcmin were measured. We show that the UV CMDs describe different evolutionary stages in a better manner than the 'classical' (V, B-V) diagram. We use HB stars, with known spectroscopic Teff, to check the validity of the colour zero-point. A review of all known UV-bright star candidates in M5 is made and some of their parameters are catalogued. Six new stars of this kind are suspected on the basis of their position on the CMD. New assessment of the cluster reddening and metallicity is done using the (U-B, B-V) diagram. We find [Fe/H]= -1.38, which confirms the Zinn & West (1984) value contrasting with recent spectroscopic estimates. In an effort to clarify the question of the gap in the BHB stellar distribution and to investigate some other peculiarities, we use the relatively long-base colour index U-V. A comparison of the unreddened (V, U-V) distribution of HB stars with a canonical ZAHB model (Dorman et al. 1993) reveals that the hottest stars rise above the model line. We find this similar to the 'u-jump' found in the Stroemgren photometry (Grundahl et al. 1998, 1999). (U-B)o indeces of 18 BHB stars with (B-V)o in [-0.02, 0.18] were used to estimate their ultraviolet deficiency. It is shown that low gravity log g < 2 Kurucz's atmospheric models fit well the observed distribution of these stars along the two-colour diagram.Comment: 9 pages, 7 EPS figures. MNRAS accepte

    Condensation in nongeneric trees

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    We study nongeneric planar trees and prove the existence of a Gibbs measure on infinite trees obtained as a weak limit of the finite volume measures. It is shown that in the infinite volume limit there arises exactly one vertex of infinite degree and the rest of the tree is distributed like a subcritical Galton-Watson tree with mean offspring probability m<1m<1. We calculate the rate of divergence of the degree of the highest order vertex of finite trees in the thermodynamic limit and show it goes like (1m)N(1-m)N where NN is the size of the tree. These trees have infinite spectral dimension with probability one but the spectral dimension calculated from the ensemble average of the generating function for return probabilities is given by 2β22\beta -2 if the weight wnw_n of a vertex of degree nn is asymptotic to nβn^{-\beta}.Comment: 57 pages, 14 figures. Minor change

    Search for Invisible Decays of η\eta and η\eta^\prime in J/ψϕηJ/\psi \to \phi\eta and ϕη\phi \eta^\prime

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    Using a data sample of 58×10658\times 10^6 J/ψJ/\psi decays collected with the BES II detector at the BEPC, searches for invisible decays of η\eta and η\eta^\prime in J/ψJ/\psi to ϕη\phi\eta and ϕη\phi\eta^\prime are performed. The ϕ\phi signals, which are reconstructed in K+KK^+K^- final states, are used to tag the η\eta and η\eta^\prime decays. No signals are found for the invisible decays of either η\eta or η\eta^\prime, and upper limits at the 90% confidence level are determined to be 1.65×1031.65 \times 10^{-3} for the ratio B(ηinvisible)B(ηγγ)\frac{B(\eta\to \text{invisible})}{B(\eta\to\gamma\gamma)} and 6.69×1026.69\times 10^{-2} for B(ηinvisible)B(ηγγ)\frac{B(\eta^\prime\to \text{invisible})}{B(\eta^\prime\to\gamma\gamma)}. These are the first searches for η\eta and η\eta^\prime decays into invisible final states.Comment: 5 pages, 4 figures; Added references, Corrected typo

    Observation of Two New N* Peaks in J/psi -> ppinˉp pi^- \bar n and pˉπ+n\bar p\pi^+n Decays

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    The πN\pi N system in decays of J/ψNˉNπJ/\psi\to\bar NN\pi is limited to be isospin 1/2 by isospin conservation. This provides a big advantage in studying NπNN^*\to \pi N compared with πN\pi N and γN\gamma N experiments which mix isospin 1/2 and 3/2 for the πN\pi N system. Using 58 million J/ψJ/\psi decays collected with the Beijing Electron Positron Collider, more than 100 thousand J/ψpπnˉ+c.c.J/\psi \to p \pi^- \bar n + c.c. events are obtained. Besides two well known NN^* peaks at 1500 MeV and 1670 MeV, there are two new, clear NN^* peaks in the pπp\pi invariant mass spectrum around 1360 MeV and 2030 MeV. They are the first direct observation of the N(1440)N^*(1440) peak and a long-sought "missing" NN^* peak above 2 GeV in the πN\pi N invariant mass spectrum. A simple Breit-Wigner fit gives the mass and width for the N(1440)N^*(1440) peak as 1358±6±161358\pm 6 \pm 16 MeV and 179±26±50179\pm 26\pm 50 MeV, and for the new NN^* peak above 2 GeV as 2068±340+152068\pm 3^{+15}_{-40} MeV and 165±14±40165\pm 14\pm 40 MeV, respectively

    The influence of gene expression time delays on Gierer-Meinhardt pattern formation systems

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    There are numerous examples of morphogen gradients controlling long range signalling in developmental and cellular systems. The prospect of two such interacting morphogens instigating long range self-organisation in biological systems via a Turing bifurcation has been explored, postulated, or implicated in the context of numerous developmental processes. However, modelling investigations of cellular systems typically neglect the influence of gene expression on such dynamics, even though transcription and translation are observed to be important in morphogenetic systems. In particular, the influence of gene expression on a large class of Turing bifurcation models, namely those with pure kinetics such as the Gierer–Meinhardt system, is unexplored. Our investigations demonstrate that the behaviour of the Gierer–Meinhardt model profoundly changes on the inclusion of gene expression dynamics and is sensitive to the sub-cellular details of gene expression. Features such as concentration blow up, morphogen oscillations and radical sensitivities to the duration of gene expression are observed and, at best, severely restrict the possible parameter spaces for feasible biological behaviour. These results also indicate that the behaviour of Turing pattern formation systems on the inclusion of gene expression time delays may provide a means of distinguishing between possible forms of interaction kinetics. Finally, this study also emphasises that sub-cellular and gene expression dynamics should not be simply neglected in models of long range biological pattern formation via morphogens

    Influence of history on saccade countermanding performance in humans and macaque monkeys

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    AbstractThe stop-signal or countermanding task probes the ability to control action by requiring subjects to withhold a planned movement in response to an infrequent stop signal which they do with variable success depending on the delay of the stop signal. We investigated whether performance of humans and macaque monkeys in a saccade countermanding task was influenced by stimulus and performance history. In spite of idiosyncrasies across subjects several trends were evident in both humans and monkeys. Response time decreased after successive trials with no stop signal. Response time increased after successive trials with a stop signal. However, post-error slowing was not observed. Increased response time was observed mainly or only after cancelled (signal inhibit) trials and not after noncancelled (signal respond) trials. These global trends were based on rapid adjustments of response time in response to momentary fluctuations in the fraction of stop signal trials. The effects of trial sequence on the probability of responding were weaker and more idiosyncratic across subjects when stop signal fraction was fixed. However, both response time and probability of responding were influenced strongly by variations in the fraction of stop signal trials. These results indicate that the race model of countermanding performance requires extension to account for these sequential dependencies and provide a basis for physiological studies of executive control of countermanding saccade performance

    Novel universality class of absorbing transitions with continuously varying critical exponents

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    The well-established universality classes of absorbing critical phenomena are directed percolation (DP) and directed Ising (DI) classes. Recently, the pair contact process with diffusion (PCPD) has been investigated extensively and claimed to exhibit a new type of critical phenomena distinct from both DP and DI classes. Noticing that the PCPD possesses a long-term memory effect, we introduce a generalized version of the PCPD (GPCPD) with a parameter controlling the memory effect. The GPCPD connects the DP fixed point to the PCPD point continuously. Monte Carlo simulations show that the GPCPD displays novel type critical phenomena which are characterized by continuously varying critical exponents. The same critical behaviors are also observed in models where two species of particles are coupled cyclically. We suggest that the long-term memory may serve as a marginal perturbation to the ordinary DP fixed point.Comment: 13 pages + 10 figures (Full paper version

    Systematics of pion emission in heavy ion collisions in the 1A GeV regime

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    Using the large acceptance apparatus FOPI, we study pion emission in the reactions (energies in GeV/nucleon are given in parentheses): 40Ca+40Ca (0.4, 0.6, 0.8, 1.0, 1.5, 1.93), 96Ru+96Ru (0.4, 1.0, 1.5), 96Zr+96Zr (0.4, 1.0, 1.5), 197Au+197Au (0.4, 0.6, 0.8, 1.0, 1.2, 1.5). The observables include longitudinal and transverse rapidity distributions and stopping, polar anisotropies, pion multiplicities, transverse momentum spectra, ratios for positively and negatively charged pions of average transverse momenta and of yields, directed flow, elliptic flow. The data are compared to earlier data where possible and to transport model simulations.Comment: 56 pages,42 figures; to be published in Nuclear Physics

    Partial wave analysis of J/\psi \to \gamma \phi \phi

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    Using 5.8×107J/ψ5.8 \times 10^7 J/\psi events collected in the BESII detector, the radiative decay J/ψγϕϕγK+KKS0KL0J/\psi \to \gamma \phi \phi \to \gamma K^+ K^- K^0_S K^0_L is studied. The ϕϕ\phi\phi invariant mass distribution exhibits a near-threshold enhancement that peaks around 2.24 GeV/c2c^{2}. A partial wave analysis shows that the structure is dominated by a 0+0^{-+} state (η(2225)\eta(2225)) with a mass of 2.240.02+0.030.02+0.032.24^{+0.03}_{-0.02}{}^{+0.03}_{-0.02} GeV/c2c^{2} and a width of 0.19±0.030.04+0.060.19 \pm 0.03^{+0.06}_{-0.04} GeV/c2c^{2}. The product branching fraction is: Br(J/ψγη(2225))Br(η(2225)ϕϕ)=(4.4±0.4±0.8)×104Br(J/\psi \to \gamma \eta(2225))\cdot Br(\eta(2225)\to \phi\phi) = (4.4 \pm 0.4 \pm 0.8)\times 10^{-4}.Comment: 11 pages, 4 figures. corrected proof for journa
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