Frequency dependence of the photonic noise spectrum in an absorbing or amplifying diffusive medium

A theory is presented for the frequency dependence of the power spectrum of photon current fluctuations originating from a disordered medium. Both the cases of an absorbing medium (“grey body”) and of an amplifying medium (“random laser”) are considered in a waveguide geometry. The semiclassical approach (based on a Boltzmann-Langevin equation) is shown to be in complete agreement with a fully quantum mechanical theory, provided that the effects of wave localization can be neglected. The width of the peak in the power spectrum around zero frequency is much smaller than the inverse coherence time, characteristic for black-body radiation. Simple expressions for the shape of this peak are obtained, in the absorbing case, for waveguide lengths large compared to the absorption length, and, in the amplifying case, close to the laser threshold. Received 8 August 2000     

Localization of polymers in a finite medium with fixed random obstacles

In this paper we investigate the conformation statistics of a Gaussian chain embedded in a medium of finite size, in the presence of quenched random obstacles. The similarities and differences between the case of random obstacles and the case of a Gaussian random potential are elucidated. The connection with the density of states of electrons in a metal with random repulsive impurities of finite range is discussed. We also interpret the results obtained in some previous numerical simulations. Received 14 August 2001     

Selective advantage of topological disorder in biological evolution

We examine a model of biological evolution of Eigen's quasispecies in a so-called holey fitness landscape, where the fitness of a site is either 0 (lethal site) or a uniform positive constant (viable site). The evolution dynamics is therefore determined by the topology of the genome space which is modelled by the random Bethe lattice. We use the effective medium and single-defect approximations to find the criteria under which the localized quasispecies cloud is created. We find that shorter genomes, which are more robust to random mutations than average, represent a selective advantage which we call “topological”. A way of assessing empirically the relative importance of reproductive success and topological advantage is suggested. Received 9 August 2002 / Received in final form 7 November 2002 Published online 14 February 2003 RID="a" ID="a"e-mail: slanina@fzu.cz     

Helix coil mixing in twist-storing polymers

Twist-storing polymers respond with elastic energy penalty to coherent or random twisting along the local chain axis away from its equilibrium, which can be straight (as in “ribbons”) or helical (as in DNA and other biopolymers). Here we study the equilibrium conformation of such polymers, focusing on the thermodynamic balance between twist and writhe, resulting from the competition between the random coil entropy and the potential energy stored in superhelical portions of the polymer chain. Two macroscopic variables characterise such a chain, the end-to-end distance R and the link number Lk, which is a topological invariant of a given polymer with clamped ends. We find that with increasing link number Lk, the chain accommodates its excess twist in growing plectonemes, unless forced out of this state by stretching its end-to-end distance R. We calculate the force-extension relation, which exhibits crossovers between different deformation regimes. Received 16 November 2000 and Received in final form 6 February 2001     

Glassy effects in the swelling/collapse dynamics of homogeneous polymers

We investigate, using numerical simulations and analytical arguments, a simple one-dimensional model for the swelling or the collapse of a closed polymer chain of size N, representing the dynamical evolution of a polymer in a Θ-solvent that is rapidly changed into a good solvent (swelling) or a bad solvent (collapse). In the case of swelling, the density profile for intermediate times is parabolic and expands in space as t ^1/3, as predicted by a Flory-like continuum theory. The dynamics slows down after a time ∝N ² when the chain becomes stretched, and the polymer gets stuck in metastable “zig-zag” configurations, from which it escapes through thermal activation. The size of the polymer in the final stages is found to grow as . In the case of collapse, the chain very quickly (after a time of order unity) breaks up into clusters of monomers (“pearls”). The evolution of the chain then proceeds through a slow growth of the size of these metastable clusters, again evolving as the logarithm of time. We enumerate the total number of metastable states as a function of the extension of the chain, and deduce from this computation that the radius of the chain should decrease as 1/ln(ln t). We compute the total number of metastable states with a given value of the energy, and find that the complexity is non-zero for arbitrary low energies. We also obtain the distribution of cluster sizes, that we compare to simple “cut-in-two” coalescence models. Finally, we determine the aging properties of the dynamical structure. The subaging behaviour that we find is attributed to the tail of the distribution at small cluster sizes, corresponding to anomalously “fast” clusters (as compared to the average). We argue that this mechanism for subaging might hold in other slowly coarsening systems. Received 23 October 2000     

Probability distribution of inherent states in models of granular media and glasses

The present paper develops a Statistical Mechanics approach to the inherent states of glassy systems and granular materials by following the original ideas proposed by Edwards for granular media. We consider three lattice models (a diluted spin glass, a system of hard spheres under gravity and a hard-spheres binary mixture under gravity) introduced to describe glassy and granular systems. They are evolved using a “tap dynamics” analogous to that of experiments on granular media. We show that the asymptotic states reached in such a dynamics are not dependent on the particular sample history and are characterized by a few thermodynamical parameters. We assume that under stationarity these systems are distributed in their inherent states satisfying the principle of maximum entropy. This leads to a generalized Gibbs distribution characterized by new “thermodynamical” parameters, called “configurational temperatures” (related to Edwards compactivity for granular materials). Finally, we show by Monte Carlo calculations that the average of macroscopic quantities over the tap dynamics and over such distribution indeed coincide. In particular, in the diluted spin glass and in the system of hard spheres under gravity, the asymptotic states reached by the system are found to be described by a single “configurational temperature”. Whereas in the hard-spheres binary mixture under gravity the asymptotic states reached by the system are found to be described by two thermodynamic parameters, coinciding with the two configurational temperatures which characterize the distribution among the inherent states when the principle of maximum entropy is satisfied under the constraint that the energies of the two species are independently fixed. Received 19 March 2002 and Received in final form 14 June 2002     

Medium effects in the production and π0γ decay of ω-mesons in pA collisions in the GeV region

The ω resonance production and its π⁰γ decay in pA reactions close to threshold is considered within the Intranuclear Cascade (INC) model. The π⁰γ invariant-mass distribution shows two components which correspond to the ω decay “inside” and “outside” the nucleus, respectively. The “inside” component is distorted by medium effects, which introduce a mass shift as well as collisional broadening for the ω-meson and its decaying pion. The relative contribution of the “inside” component is analyzed in detail for different kinematical conditions and nuclear targets. It is demonstrated that a measurement of the correlation in azimuthal angle between the π⁰ and γ momenta allows to separate events related to the “inside”ω decay from different sources of background when uncorrelated π⁰'s and γ's are produced. Received: 2 April 2001 / Accepted: 5 June 2001     

Dynamical properties of the slithering-snake algorithm: A numerical test of the activated-reptation hypothesis

Correlations in the motion of reptating polymers in a melt are investigated by means of Monte Carlo simulations of the three-dimensional slithering-snake version of the bond-fluctuation model. Surprisingly, the slithering-snake dynamics becomes inconsistent with classical reptation predictions at high chain overlap (created either by chain length N or by the volume fraction φ of occupied lattice sites), where the relaxation times increase much faster than expected. This is due to the anomalous curvilinear diffusion in a finite time window whose upper bound (N) is set by the density of chain ends φ/N. Density fluctuations created by passing chain ends allow a reference polymer to break out of the local cage of immobile obstacles created by neighboring chains. The dynamics of dense solutions of “snakes” at t ≪ is identical to that of a benchmark system where all chains but one are frozen. We demonstrate that the subdiffusive dynamical regime is caused by the slow creeping of a chain out of its correlation hole. Our results are in good qualitative agreement with the activated-reptation scheme proposed recently by Semenov and Rubinstein (Eur. Phys. J. B, 1 (1998) 87). Additionally, we briefly comment on the relevance of local relaxation pathways within a slithering-snake scheme. Our preliminary results suggest that a judicious choice of the ratio of local to slithering-snake moves is crucial to equilibrate a melt of long chains efficiently. Received: 18 December 2002 / Accepted: 3 April 2003 / Published online: 12 May 2003 RID="a" ID="a"e-mail: jwittmer@dpm.univ-lyon1.fr RID="b" ID="b"Current address: University of Illinois at Urbana-Champaign.     

Diffusion, localization and dispersion relations on “small-world” lattices

The spectral properties of the Laplacian operator on “small-world” lattices, that is mixtures of unidimensional chains and random graphs structures are investigated numerically and analytically. A transfer matrix formalism including a self-consistent potential à la Edwards is introduced. In the extended region of the spectrum, an effective medium calculation provides the density of states and pseudo relations of dispersion for the eigenmodes in close agreement with the simulations. Localization effects, which are due to connectivity fluctuations of the sites are shown to be quantitatively described by the single defect approximation recently introduced for random graphs. Received 23 March 1999     

The role of pinning and instability in a class of non-equilibrium growth models

We study the dynamics of a growing crystalline facet where the growth mechanism is controlled by the geometry of the local curvature. A continuum model, in (2+1) dimensions, is developed in analogy with the Kardar-Parisi-Zhang (KPZ) model is considered for the purpose. Following standard coarse graining procedures, it is shown that in the large time, long distance limit, the continuum model predicts a curvature independent KPZ phase, thereby suppressing all explicit effects of curvature and local pinning in the system, in the “perturbative” limit. A direct numerical integration of this growth equation, in 1+1 dimensions, supports this observation below a critical parametric range, above which generic instabilities, in the form of isolated pillared structures lead to deviations from standard scaling behaviour. Possibilities of controlling this instability by introducing statistically “irrelevant" (in the sense of renormalisation groups) higher ordered nonlinearities have also been discussed. Received 23 April 2002 / Received in final form 24 July 2002 Published online 31 October 2002 RID="a" ID="a"e-mail: akc@mpipks-dresden.mpg.de     

Energy landscapes, lowest gaps, and susceptibility of elastic manifolds at zero temperature

We study the effect of an external field on (1 + 1) and (2 + 1) dimensional elastic manifolds, at zero temperature and with random bond disorder. Due to the glassy energy landscape the configuration of a manifold changes often in abrupt, “first order”-type of large jumps when the field is applied. First the scaling behavior of the energy gap between the global energy minimum and the next lowest minimum of the manifold is considered, by employing exact ground state calculations and an extreme statistics argument. The scaling has a logarithmic prefactor originating from the number of the minima in the landscape, and reads ΔE ₁∼L ^θ[ln(L _z L ^{- ζ})]^-1/2, where ζ is the roughness exponent and θ is the energy fluctuation exponent of the manifold, L is the linear size of the manifold, and L_z is the system height. The gap scaling is extended to the case of a finite external field and yields for the susceptibility of the manifolds ∼L ^{2D + 1 - θ}[(1 - ζ)ln(L)]^1/2. We also present a mean field argument for the finite size scaling of the first jump field, h ₁∼L ^{d - θ}. The implications to wetting in random systems, to finite-temperature behavior and the relation to Kardar-Parisi-Zhang non-equilibrium surface growth are discussed. Received December 2000 and Received in final form April 2001     

Melting and unzipping of DNA

Existing experimental studies of the thermal denaturation of DNA yield sharp steps in the melting curve suggesting that the melting transition is first order. This transition has been theoretically studied since the early sixties, mostly within an approach in which the microscopic configurations of a DNA molecule consist of an alternating sequence of non-interacting bound segments and denaturated loops. Studies of these models neglect the repulsive, self-avoiding, interaction between different loops and segments and have invariably yielded continuous denaturation transitions. In the present study we take into account in an approximate way the excluded-volume interaction between denaturated loops and the rest of the chain. This is done by exploiting recent results on scaling properties of polymer networks of arbitrary topology. We also ignore the heterogeneity of the polymer. We obtain a first-order melting transition in d = 2 dimensions and above, consistent with the experimental results. We also consider within our approach the unzipping transition, which takes place when the two DNA strands are pulled apart by an external force acting on one end. We find that the under equilibrium condition the unzipping transition is also first order. Although the denaturation and unzipping transitions are thermodynamically first order, they do exhibit critical fluctuations in some of their properties. For instance, the loop size distribution decays algebraically at the transition and the length of the denaturated end segment diverges as the transition is approached. We evaluate these critical properties within our approach. Received 21 August 2001 and Received in final form 26 January 2002     

Genetic Algorithms as a tool in the study of aperiodic order,with application to the case of X-Ray diffraction spectra of GaAs-AlAs multilayer heterostructures

We present the first application of Genetic Algorithms to the analysis of data from an aperiodically ordered system, high resolution X-Ray diffraction spectra from multilayer heterostructures arranged according to a deterministic or random scheme. This method paves the way to the solution of the “inverse problem”, that is the retrieval of the generating disorder from the investigation of the spectra of an unknown sample having non crystallographic, non quasi-crystallographic order. Received 18 March 2002 / Received in final form 3 July 2002 Published online 31 October 2002 RID="a" ID="a"e-mail: Evelyne.Lutton@inria.fr RID="b" ID="b"CNRS UMR 8502     

The escape transition of a polymer: A unique case of non-equivalence between statistical ensembles

A flexible polymer chain under good solvent conditions, end-grafted on a flat repulsive substrate surface and compressed by a piston of circular cross-section with radius L may undergo the so-called “escape transition” when the height of the piston D above the substrate and the chain length N are in a suitable range. In this transition, the chain conformation changes from a quasi-two-dimensional self-avoiding walk of “blobs” of diameter D to an inhomogeneous “flower” state, consisting of a “stem” (stretched string of blobs extending from the grafting site to the piston border) and a “crown” outside of the confining piston. The theory of this transition is developed using a Landau free-energy approach, based on a suitably defined (global) order parameter and taking also effects due to the finite chain length N into account. The parameters of the theory are determined in terms of known properties of limiting cases (unconfined mushroom, chain confined between infinite parallel walls). Due to the non-existence of a local order parameter density, the transition has very unconventional properties (negative compressibility in equilibrium, non-equivalence between statistical ensembles in the thermodynamic limit, etc.). The reasons for this very unusual behavior are discussed in detail. Using Molecular Dynamics (MD) simulation for a simple bead-spring model, with N in the range 50 N 300 , a comprehensive study of both static and dynamic properties of the polymer chain was performed. Even though for the considered rather short chains the escape transition is still strongly rounded, the order parameter distribution does reveal the emerging transition clearly. Time autocorrelation functions of the order parameter and first passage times and their distribution indicate clearly the strong slowing down associated with the chain escape. The theory developed here is in good agreement with all these simulation results.     

Aging and non-linear glassy dynamics in a mean field model

The mean field approach of glassy dynamics successfully describes systems which are out-of-equilibrium in their low temperature phase. In some cases an aging behaviour is found, with no stationary regime ever reached. In the presence of dissipative forces however, the dynamics is indeed stationary, but still out-of-equilibrium, as inferred by a significant violation of the fluctuation dissipation theorem. The mean field dynamics of a particle in a random but short-range correlated environment, offers the opportunity of observing both the aging and driven stationary regimes. Using a geometrical approach previously introduced by the author, we study here the relation between these two situations, in the pure relaxational limit, i.e. the zero temperature case. In the stationary regime, the velocity (v)-force (F) characteristics is a power law v∼F ⁴, while the characteristic times scale like powers of v, in agreement with an early proposal by Horner. The cross-over between the aging, linear-response regime and the non-linear stationary regime is smooth, and we propose a parametrization of the correlation functions valid in both cases, by means of an “effective time”. We conclude that aging and non-linear response are dual manifestations of a single out-of-equilibrium state, which might be a generic situation. Received 7 May 2000 and Received in final form 22 August 2000     

Switching of banana liquid crystal mesophases under field

Taking advantage of the great number of bent-core or “banana" compounds synthesized and studied in the laboratory, we describe their behaviour under the application of an external electric field. If the field were a static one, we would work within the frame of an equilibrium phase diagram in a (field E, temperature T) space where some phases would be simple dielectrics and others ferroelectric ones with a macroscopic polarization, either spontaneous or induced by the field. In this paper, we deal with the basic responses of “banana” liquid crystals under the application of a low frequency (1 to 100 Hz) AC field. Firstly square-wave voltages allow us to locate the phase boundary between dielectric (at lower field) and ferroelectric phases (higher field) at a given temperature and field threshold. Then we apply slowly varying AC voltages with shapes like triangle or “triple-plateau” to check out the stability of the induced ferroelectric phase versus field removal. Three behaviours are encountered, the unstable one (short lifetime of the high-field ferroelectric phase) where the macroscopic polarization is destroyed and then rebuilt in the opposite direction during each half period and usually called “antiferroelectric”; the stable one (long lifetime) with a polarization that rotates at constant modulus which is labeled as “ferroelectric” and a new one where the macroscopic polarization is proportional to the applied fied, we named this behaviour as “superparaelectric”. Let us stress that these observations apply to the ferroelectric phases of the (E, T) phase diagram not to the zero field (0,T) phases observed in the usual phase characterization experiments except for an eventual spontaneous ferroelectric phase. Received 18 April 2002 and Received in final form 17 January 2003 Published online: 16 April 2003 RID="a" ID="a"e-mail: marcerou@crpp.u-bordeaux.fr RID="b" ID="b"URL: http://www.crpp-bordeaux.cnrs.fr     

Structures and energetics of carbon bridged C 60 clusters

The structures and energetics of carbon bridged C₆₀ clusters (C ₆₀ ) _n C_m have been studied by simulated annealing technique within the tight-binding molecular-dynamics. The “sp² addition” ball-and-chain dimers exhibit odd-even alternations over the number of chain atoms, with the dimers containing even chain atoms more stable against dissociation than their immediate neighbors containing odd chain atoms. In addition to the usual “sp² addition” dimers, a pentagon-linked C₁₂₁ isomer and a hexagon-linked C₁₂₂ isomer are also found to be stable. Based on our tight-binding calculations, trimers and larger clusters can be simply regarded as being made up of independent or weakly interacting dimers, if the C-C₆₀ joints on a single cage are not too close to each other. Large C₆₀ clusters connected by chains each containing only one or two carbon atoms have similar stability to that of constituent dimers, indicating the possibility to form stable C₆₀-carbon polymers. Received 17 January 2001 and Received in final form 26 February 2001     

Mixing and sorting of bidisperse two-dimensional bubbles

We have examined a number of candidates for the minimum-surface-energy arrangement of two-dimensional clusters composed of N bubbles of area 1 and N bubbles of area λ ( λ≤1). These include hexagonal bubbles sorted into two monodisperse honeycomb tilings, and various mixed periodic tilings with at most four bubbles per unit cell. We identify, as a function of λ, the minimal configuration for N → ∞. For finite N, the energy of the external (i.e., cluster-gas) boundary and that of the interface between honeycombs in “phase-separated” clusters have to be taken into account. We estimate these contributions and find the lowest total energy configuration for each pair (N,λ). As λ is varied, this alternates between a circular cluster of one of the mixed tilings, and “partial wetting” of the monodisperse honeycomb of bubble area 1 by the monodisperse honeycomb of bubble area λ. Received 1 August 2002 RID="a" ID="a"e-mail: paulo@ist.utl.pt     

On the quest of production of superheavy nuclei in reactions of 48Ca with the heaviest cctinide targets

The sequence of radioactive decays of an unknown isotope produced in a rare fusion reaction to known lighter isotopes is used to identify mass and atomic number of the mother isotope, which has been separated before from the bulk of other reaction products by an in-flight recoil separator. By this technique the elements 107 to 112 were produced by single atom decay-chain analysis. Such a correlation technique reaches its limit by the occurrence of accidental sequences and it collapses beyond a maximum possible correlation time, at which a true event cannot be distinguished anymore from a random event. ⁴⁸Ca-induced fusion reactions with actinides are discussed. In 1983 at GSI, Darmstadt and LBL, Berkeley, ⁴⁸Ca/²⁴⁸Cm-experiments (II) were performed, which are compared to recent ⁴⁸Ca-experiments at FLNR-Dubna (I) irradiating ²⁴⁴Pu, ²⁴²Pu, and ²³⁸U. In these experiments production of isotopes of superheavy elements 112 and 114 is claimed. Our analysis of accidental sequences in ⁴⁸Ca-induced reactions is presented, which is at variance with the published analysis from FLNR-Dubna. We find that the maximum correlation time using continuous beams at today existing separation systems is not in the one-hour regime, but in the few-minute regime. The five spontaneous fission events observed in the FLNR experiments are preceded by signals in the (1–16)-minute range. These times are shown to be longer than the maximum possible correlation times. The preceding signals are decoupled from the spontaneous fission signal and carry no information on the spontaneous fission events observed. Moreover, random probabilities of 0.2 to 0.6 for the signals preceding the fission events indicate that the correlations are of random origin. The evidence to have discovered element 114 in the reported experiments is classified “very weak”. Received: 13 October 1999