Is it really possible to grow isotropic on-lattice diffusion-limited aggregates?

In a recent paper (Bogoyavlenskiy V A 2002 \JPA \textbf{35} 2533), an algorithm aiming to generate isotropic clusters of the on-lattice diffusion-limited aggregation (DLA) model was proposed. The procedure consists of aggregation probabilities proportional to the squared number of occupied sites ($k^2$). In the present work, we analyzed this algorithm using the noise reduced version of the DLA model and large scale simulations. In the noiseless limit, instead of isotropic patterns, a $45^\circ$ ($30^\circ$) rotation in the anisotropy directions of the clusters grown on square (triangular) lattices was observed. A generalized algorithm, in which the aggregation probability is proportional to $k^\nu$, was proposed. The exponent $\nu$ has a nonuniversal critical value $\nu_c$, for which the patterns generated in the noiseless limit exhibit the original (axial) anisotropy for $\nu<\nu_c$ and the rotated one (diagonal) for $\nu>\nu_c$. The values $\nu_c = 1.395\pm0.005$ and $\nu_c = 0.82\pm 0.01$ were found for square and triangular lattices, respectively. Moreover, large scale simulations show that there are a nontrivial relation between noise reduction and anisotropy direction. The case $\nu=2$ (\bogo's rule) is an example where the patterns exhibit the axial anisotropy for small and the diagonal one for large noise reduction.Comment: 12 pages, 8 figure

Newcastle Disease Virus in Madagascar: Identification of an Original Genotype Possibly Deriving from a Died Out Ancestor of Genotype IV

In Madagascar, Newcastle disease (ND) has become enzootic after the first documented epizootics in 1946, with recurrent annual outbreaks causing mortality up to 40%. Four ND viruses recently isolated in Madagascar were genotypically and pathotypically characterised. By phylogenetic inference based on the F and HN genes, and also full-genome sequence analyses, the NDV Malagasy isolates form a cluster distant enough to constitute a new genotype hereby proposed as genotype XI. This new genotype is presumably deriving from an ancestor close to genotype IV introduced in the island probably more than 50 years ago. Our data show also that all the previously described neutralising epitopes are conserved between Malagasy and vaccine strains. However, the potential implication in vaccination failures of specific amino acid substitutions predominantly found on surface-exposed epitopes of F and HN proteins is discussed