5,621 research outputs found

    Imperfect Imitation Can Enhance Cooperation

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    The promotion of cooperation on spatial lattices is an important issue in evolutionary game theory. This effect clearly depends on the update rule: it diminishes with stochastic imitative rules whereas it increases with unconditional imitation. To study the transition between both regimes, we propose a new evolutionary rule, which stochastically combines unconditional imitation with another imitative rule. We find that, surprinsingly, in many social dilemmas this rule yields higher cooperative levels than any of the two original ones. This nontrivial effect occurs because the basic rules induce a separation of timescales in the microscopic processes at cluster interfaces. The result is robust in the space of 2x2 symmetric games, on regular lattices and on scale-free networks.Comment: 4 pages, 4 figure

    Human behavior in Prisoner's Dilemma experiments suppresses network reciprocity

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    During the last few years, much research has been devoted to strategic interactions on complex networks. In this context, the Prisoner's Dilemma has become a paradigmatic model, and it has been established that imitative evolutionary dynamics lead to very different outcomes depending on the details of the network. We here report that when one takes into account the real behavior of people observed in the experiments, both at the mean-field level and on utterly different networks the observed level of cooperation is the same. We thus show that when human subjects interact in an heterogeneous mix including cooperators, defectors and moody conditional cooperators, the structure of the population does not promote or inhibit cooperation with respect to a well mixed population.Comment: 5 Pages including 4 figures. Submitted for publicatio

    Las formaciones cuaternarias del delta del Llobregat

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    IGR J19294+1816: a new Be-X ray binary revealed through infrared spectroscopy

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    The aim of this work is to characterize the counterpart to the INTEGRAL High Mass X-ray Binary candidate IGR J19294+1816 so as to establish its true nature. We obtained H band spectra of the selected counterpart acquired with the NICS instrument mounted on the Telescopio Nazionale Galileo (TNG) 3.5-m telescope which represents the first infrared spectrum ever taken of this source. We complement the spectral analysis with infrared photometry from UKIDSS, 2MASS, WISE and NEOWISE databases. We classify the mass donor as a Be star. Subsequently, we compute its distance by properly taking into account the contamination produced by the circumstellar envelope. The findings indicate that IGR J19294+1816 is a transient source with a B1Ve donor at a distance of d=11±1d = 11 \pm 1 kpc, and luminosities of the order of 10363710^{36-37} erg s1^{-1}, displaying the typical behaviour of a Be X-ray binary.Comment: 8 pages, 6 figures, accepted to be published in MNRA

    Electron scattering in isotonic chains as a probe of the proton shell structure of unstable nuclei

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    Electron scattering on unstable nuclei is planned in future facilities of the GSI and RIKEN upgrades. Motivated by this fact, we study theoretical predictions for elastic electron scattering in the N=82, N=50, and N=14 isotonic chains from very proton-deficient to very proton-rich isotones. We compute the scattering observables by performing Dirac partial-wave calculations. The charge density of the nucleus is obtained with a covariant nuclear mean-field model that accounts for the low-energy electromagnetic structure of the nucleon. For the discussion of the dependence of scattering observables at low-momentum transfer on the gross properties of the charge density, we fit Helm model distributions to the self-consistent mean-field densities. We find that the changes shown by the electric charge form factor along each isotonic chain are strongly correlated with the underlying proton shell structure of the isotones. We conclude that elastic electron scattering experiments in isotones can provide valuable information about the filling order and occupation of the single-particle levels of protons.Comment: 13 pages; 19 figure

    Recoverin Regulates Light-dependent Phosphodiesterase Activity in Retinal Rods

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    The Ca2+-binding protein recoverin may regulate visual transduction in retinal rods and cones, but its functional role and mechanism of action remain controversial. We compared the photoresponses of rods from control mice and from mice in which the recoverin gene was knocked out. Our analysis indicates that Ca2+-recoverin prolongs the dark-adapted flash response and increases the rod's sensitivity to dim steady light. Knockout rods had faster Ca2+ dynamics, indicating that recoverin is a significant Ca2+ buffer in the outer segment, but incorporation of exogenous buffer did not restore wild-type behavior. We infer that Ca2+-recoverin potentiates light-triggered phosphodiesterase activity, probably by effectively prolonging the catalytic activity of photoexcited rhodopsin

    Study of the neutron skin thickness of 208{}^{208}Pb in mean field models

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    We study whether the neutron skin thickness Δrnp\Delta r_{np} of 208{}^{208}Pb originates from the bulk or from the surface of the neutron and proton density distributions in mean field models. We find that the size of the bulk contribution to Δrnp\Delta r_{np} of 208{}^{208}Pb strongly depends on the slope of the nuclear symmetry energy, while the surface contribution does not. We note that most mean field models predict a neutron density for 208{}^{208}Pb between the halo and skin type limits. We investigate the dependence of parity- violating electron scattering at the kinematics of the PREX experiment on the shape of the nucleon densities predicted by the mean field models for 208{}^{208}Pb. We find an approximate formula for the parity-violating asymmetry in terms of the central radius and the surface diffuseness of the nucleon densities of 208{}^{208}Pb in these models.Comment: 5 pages, 2 figures, proceedings MBC 2011 - Many body correlations from dilute to dense nuclear systems - IHP PARI
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