Evolution of isolated neutron stars in globular clusters: number of Accretors

With a simple model from the point of view of population synthesis we try to verify an interesting suggestion made by Pfahl & Rappaport (2001) that dim sources in globular clusters (GCs) can be isolated accreting neutron stars (NSs). Simple estimates show, that we can expect about 0.5-1 accreting isolated NS per typical GC with $M=10^5 M_{\odot}$ in correspondence with observations. Properties of old accreting isolated NSs in GCs are briefly discussed. We suggest that accreting NSs in GCs experienced significant magnetic field decay.Comment: 6 pages, no figures. Submitted to Astronomical and Astrophysical Transactions (style included

Prediction of the Supersonic Flow Base Pressure by Axisymmetric ‎Direct Numerical Simulation

Axisymmetric direct numerical simulation (DNS) has been carried out to predict supersonic base flow behavior. Substantially fine grid has been used to perform calculations for the flow with Reynolds number up to 106. Optimal grid resolution was established through test calculations for affordable run time and solution convergence determined by the vorticity value. Numerical scheme provides fourth-order approximation for dissipative, fifth-order for convective and second-order for unsteady terms of conservation equations. Reynolds Averaged Navier-Stokes (RANS) approach has been employed to obtain input flow profiles for DNS calculations. Series of calculations have been carried out for Mach number 1.5 with Reynolds numbers 104, 105, 106 and for Mach number 2.46 with Reynolds number 1.65×106. It has been found that local base pressure coefficient calculated by DNS is a bit overestimated in a zone close to symmetry axis in comparison with experiment while integrated base drag coefficient shows good agreement with experimental data and noticeably better than one obtained by RANS approach

Homopolymer tract length dependent enrichments in functional regions of 27 eukaryotes and their novel dependence on the organism DNA (G+C)% composition

BACKGROUND: DNA homopolymer tracts, poly(dA).poly(dT) and poly(dG).poly(dC), are the simplest of simple sequence repeats. Homopolymer tracts have been systematically examined in the coding, intron and flanking regions of a limited number of eukaryotes. As the number of DNA sequences publicly available increases, the representation (over and under) of homopolymer tracts of different lengths in these regions of different genomes can be compared. RESULTS: We carried out a survey of the extent of homopolymer tract over-representation (enrichment) and over-proportional length distribution (above expected length) primarily in the single gene documents, but including some whole chromosomes of 27 eukaryotics across the (G+C)% composition range from 20 – 60%. A total of 5.2 × 10(7 )bases from 15,560 cleaned (redundancy removed) sequence documents were analyzed. Calculated frequencies of non-overlapping long homopolymer tracts were found over-represented in non-coding sequences of eukaryotes. Long poly(dA).poly(dT) tracts demonstrated an exponential increase with tract length compared to predicted frequencies. A novel negative slope was observed for all eukaryotes between their (G+C)% composition and the threshold length N where poly(dA).poly(dT) tracts exhibited over-representation and a corresponding positive slope was observed for poly(dG).poly(dC) tracts. Tract size thresholds where over-representation of tracts in different eukaryotes began to occur was between 4 – 11 bp depending upon the organism (G+C)% composition. The higher the GC%, the lower the threshold N value was for poly(dA).poly(dT) tracts, meaning that the over-representation happens at relatively lower tract length in more GC-rich surrounding sequence. We also observed a novel relationship between the highest over-representations, as well as lengths of homopolymer tracts in excess of their random occurrence expected maximum lengths. CONCLUSIONS: We discuss how our novel tract over-representation observations can be accounted for by a few models. A likely model for poly(dA).poly(dT) tract over-representation involves the known insertion into genomes of DNA synthesized from retroviral mRNAs containing 3' polyA tails. A proposed model that can account for a number of our observed results, concerns the origin of the isochore nature of eukaryotic genomes via a non-equilibrium GC% dependent mutation rate mechanism. Our data also suggest that tract lengthening via slip strand replication is not governed by a simple thermodynamic loop energy model