Spin glasses on Bethe Lattices for large coordination number

We study spin glasses on random lattices with finite connectivity. In the infinite connectivity limit they reduce to the Sherrington Kirkpatrick model. In this paper we investigate the expansion around the high connectivity limit. Within the replica symmetry breaking scheme at two steps, we compute the free energy at the first order in the expansion in inverse powers of the average connectivity (z), both for the fixed connectivity and for the fluctuating connectivity random lattices. It is well known that the coefficient of the 1/z correction for the free energy is divergent at low temperatures if computed in the one step approximation. We find that this annoying divergence becomes much smaller if computed in the framework of the more accurate two steps breaking. Comparing the temperature dependance of the coefficients of this divergence in the replica symmetric, one step and two steps replica symmetry breaking, we conclude that this divergence is an artefact due to the use of a finite number of steps of replica symmetry breaking. The 1/z expansion is well defined also in the zero temperature limit.Comment: 17 pages and 6 figure

Jamming in frictionless packings of spheres: determination of the critical volume fraction

The jamming transition in granular packings is characterized by a sudden change in the coordination number. In this work we investigate the evolution of coordination number as function of volume fraction for frictionless packings of spheres undergoing isotropic deformation. Using the results obtained from Discrete Element Method simulations, we confirm that the coordination number depends on volume fraction by a power law with exponent α≈0.5 above the critical volume fraction and up to rather high densities. We find that the system size and loading rate do not have an important effect on the evolution of the coordination number. Polydispersity of the packing seems to cause a shift in the critical volume fraction, i.e., more heterogeneous packings jam at higher volume fractions. Finally, we propose and evaluate alternative methods to determine the critical volume fraction based on the number of rattlers, the pressure and the ratio of kinetic and potential energies. The results are all consistent with the critical volume fractions obtained from the fits of the power law to the simulation data

Isostaticity in two dimensional pile of rigid disks

We study the static structure of piles made of polydisperse disks in the rigid limit with and without friction using molecular dynamic simulations for various elasticities of the disks and pile preparation procedures. The coordination numbers are calculated to examine the isostaticity of the pile structure. For the frictionless pile, it is demonstrated that the coordination number converges to 4 in the rigid limit, which implies that the structure of rigid disk pile is isostatic. On the other hand, for the frictional case with the infinite friction constant, the coordination number depends on the preparation procedure of the pile, but we find that the structure becomes very close to isostatic with the coordination number close to 3 in the rigid limit when the pile is formed through the process that tends to make a pile of random configuration.Comment: 3 pages, 3 figures, Submitted to J. Phys. Soc. Jp

Connected Coordination: Network Structure and Group Coordination

Networks can affect a group’s ability to solve a coordination problem. We utilize laboratory experiments to study the conditions under which groups of subjects can solve coordination games. We investigate a variety of different network structures, and we also investigate coordination games with symmetric and asymmetric payoffs. Our results show that network connections facilitate coordination in both symmetric and asymmetric games. Most significantly, we find that increases in the number of network connections encourage coordination even when payoffs are highly asymmetric. These results shed light on the conditions that may facilitate coordination in real-world networks

X-ray absorption study of Ti-bearing silicate glasses

Ti K-edge XANES spectra have been collected on a series of Ti-bearing silicate glasses with metasilicate and tetrasilicate compositions. The intensity of the preedge feature in these spectra has been found to change with glass composition and varies from 29 to 58% (normalized intensity) suggesting a variation in structural environent around the absorbing atom. The pre-edge peak intensity increases for the alkali titanium tetrasilicate glasses from 35% to 58% in the order Li < Na < K < Rb, Cs whereas for the metasilicate compositions there is a maximum for the K-bearing glass. The pre-edge peak intensity remains constant for the alkaline earth titanium metasilicate glasses, Ca and Sr (34%) but increases slightly for Ba (41%). As the intensity of this feature is inversely correlated with coordination number, a comparison of the pre-edge intensity data for the investigated glasses with those of materials of known coordination number leads us to establish a regression equation and to infer that the average coordination number of Ti in these glasses ranges from 4.8 to 5.8. Large alkali cations appear to stabilize a relatively low average coordination number for Ti in silicate melts. The Ti structural environment results appear also to vary as a function of SiO2 content within the K2O-TiO2-SiO2 system. A number of physical properties of the melts from which these glasses were quenched and of other Ti-bearing silicate melts, have been determined in recent years. Clear evidence of a variable coordination number of Ti, consistent with the interpretation of the present XANES data is available from density measurements. These and other property determinations are compared with the present spectroscopic observations in an attempt to relate structure and properties in these melts which contain a major component with variable coordination number

Constitutive relations for the isotropic deformation of frictionless packings of polydisperse spheres

The isotropic compression of polydisperse packings of frictionless spheres is modeled with the Discrete Element Method (DEM). The evolution of coordination number, fraction of rattlers, isotropic fabric, and pressure (isotropic stress) is reported as function of volume fraction for different system parameters. The power law relationship, with power ≈1/2, between coordination number and volume fraction is confirmed in the jammed state for a broad range of volume fractions and for different (moderate) polydispersities. The polydispersity in the packing causes a shift of the critical volume fraction, i.e., more heterogeneous packings jam at higher volume fractions. Close to jamming, the coordination number and the jamming volume fraction itself depend on both history and rate. At larger densities, neither the deformation history nor the loading rate have a significant effect on the evolution of the coordination number.\ud \ud Concerning the fabric tensor, comparing our DEM results to theoretical predictions, good agreement for different polydispersities is observed. An analytical expression for the pressure as function of isotropic (volumetric) strain is proposed for polydisperse packings, based on the assumption of uniform deformation. We note that, besides the implicit proportionality to contact number density (or fabric), no single power-law is evidenced in the relation between pressure and isotropic strain. However, starting from zero pressure at the jamming point, a linear term with a quadratic correction describes the stress evolution rather well for a broad range of densities and for various polydispersities. Finally, an incremental evolution equation is proposed for both fabric and stress, as function of isotropic strain, and involving the coordination number and the fraction of rattlers, as starting point for further studies involving anisotropic deformations