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We theoretically investigate the single and double ionization of the He atom by antiproton impact for projectile energies ranging from $3$~keV up to $1000$~keV. We obtain accurate total cross sections by directly solving the fully correlated two-electron time-dependent Schr\"odinger equation and by performing classical trajectory Monte-Carlo calculations. The obtained quantum-mechanical results are in excellent agreement with the available experimental data. Along with the total cross sections, we also present the first fully \textit{ab initio} doubly differential data for single ionization at 10 and 100~keV impact energies. In these differential cross sections we identify the binary-encounter peak along with the anticusp minimum. Furthermore, we also point out the importance of the post-collisional electron-projectile interaction at low antiproton energies which significantly suppresses electron emission in the forward direction.

The n−3 fatty acids are not produced by mammals, although they are essential for hormone synthesis and maintenance of cell membrane structure and integrity. They have recently been shown to inhibit inflammatory reactions and also emerged as potential treatment options for inflammatory diseases, such as rheumatoid arthritis, asthma and inflammatory bowel diseases. Dendritic cells (DC) play a central role in the regulation of both innate and adaptive immunity and upon inflammatory signals they produce various soluble factors among them cytokines and chemokines that act as inflammatory or regulatory mediators. In this study we monitored the effects of α-linoleic acid, eicosapentaenoic acid and docosahexaenoic acid solubilized in a dimethyl sulfoxide (DMSO)/ethanol 1:1 mixture or as complexed by randomly methylated α-cyclodextrin (RAMEA) on the inflammatory response of human monocyte-derived dendritic cells (moDC). The use of RAMEA for enhancing aqueous solubility of n−3 fatty acids has the unambiguous advantage over applying RAMEB (the β-cyclodextrin analog), since there is no interaction with cell membrane cholesterol. In vitro differentiated moDC were left untreated or were stimulated by bacterial lipopolysaccharide and polyinosinic:polycytidylic acid, mimicking bacterial and viral infections, respectively. The response of unstimulated and activated moDC to n−3 fatty acid treatment was tested by measuring the cell surface expression of CD1a used as a phenotypic and CD83 as an activation marker of inflammatory moDC differentiation and activation by using flow cytometry. Monocyte-derived DC activation was also monitored by the secretion level of the pro- and anti-inflammatory cytokines IL-1β, TNF-α, IL-6, IL-10 and IL-12, respectively. We found that RAMEA-complexed n−3 fatty acids reduced the expression of CD1a protein in both LPS and Poly(I:C) stimulated moDC significantly, but most efficiently by eicosapentaenic acid, while no significant change in the expression of CD83 protein was observed. The production of IL-6 by LPS-activated moDC was also reduced significantly when eicosapentaenic acid was added as a RAMEA complex as compared to its DMSO-solubilized form or to the other two n−3 fatty acids either complexed or not. Based on these results n−3 fatty acids solubilized by RAMEA provide with a new tool for optimizing the anti-inflammatory effects of n−3 fatty acids exerted on human moDC and mediated through the GP120 receptor without interfering with the cell membrane structure.

We formulate a generic concept model for the deformation of a locally disordered, macroscopically homogeneous material which undergoes irreversible strain softening during plastic deformation. We investigate the influence of the degree of microstructural heterogeneity and disorder on the concomitant strain localization process (formation of a macroscopic shear band). It is shown that increased microstructural heterogeneity delays strain localization and leads to an increase of the plastic regime in the macroscopic stress-strain curves. The evolving strain localization patterns are characterized and compared to models of shear band formation published in the literature. 9 pages, 9 figures

Biodiversity has always been predominantly microbial and the scarcity of fossils from bacteria, archaea and microbial eukaryotes has prevented a comprehensive dating of the tree of life. Here we show that patterns of lateral gene transfer deduced from the analysis of modern genomes encode a novel and abundant source of information about the temporal coexistence of lineages throughout the history of life. We use new phylogenetic methods to reconstruct the history of thousands of gene families and demonstrate that dates implied by gene transfers are consistent with estimates from relaxed molecular clocks in Bacteria, Archaea and Eukaryotes. An inspection of discrepancies between transfers and clocks and a comparison with mammal fossils show that gene transfer in microbes is potentially as informative for dating the tree of life as the geological record in macroorganisms.

For geometric Lorenz attractors (including the classical Lorenz attractor) we obtain a greatly simplified proof of the central limit theorem which applies also to the more general class of codimension two singular hyperbolic attractors. We also obtain the functional central limit theorem and moment estimates, as well as iterated versions of these results. A consequence is deterministic homogenisation (convergence to a stochastic differential equation) for fast-slow dynamical systems whenever the fast dynamics is singularly hyperbolic of codimension two. Comment: Minor corrections. Published online in J. Stat. Phys

Excited states in the $T_z=-1$ nucleus $^{70}$Kr have been populated using inelastic scattering of a radioactive $^{70}$Kr beam as well as one- and two-neutron removal reactions from $^{71,72}$Kr at intermediate beam energies. The level scheme of $^{70}$Kr was constructed from the observed $\gamma$-ray transitions and coincidences. Tentative spin and parity assignments were made based on comparison with the mirror nucleus $^{70}$Se. A second $2^+$ state and a candidate for the corresponding $4^+_2$ state suggest shape coexistence in $^{70}$Kr. Comment: accepted Phys. Lett. B

The recent discovery of gravitational waves has opened new horizons for physics. Current and upcoming missions, such as LIGO, VIRGO, KAGRA, and LISA, promise to shed light on black holes of every size from stellar mass (SBH) sizes up to supermassive black holes which reside in galactic nuclei. The intermediate mass black hole (IMBH) family has not been detected beyond any reasonable doubt neither directly nor indirectly. Recent analyses suggest observational evidence for the presence of IMBHs in the centers of two Galactic globular clusters. In this paper, we investigate the possibility that globular clusters were born with a central IMBH, which undergo repeated merger events with SBHs in the cluster core. By means of a semi-analytical method, we follow the evolution of the primordial cluster population in the galactic potential and the Gravitational Wave (GW) mergers of the binary IMBH-SBH systems. Our models predict ≈1000 IMBHs within 1 kpc from the Galactic Center. Our results show that the IMBH-SBH merger rate density changes from \(\mathcal{R} \approx 1000\,\mathrm{Gpc}^{-3}\mathrm{yr}^{-1}\) beyond \(z\approx 2\) to \(\mathcal{R} \approx 1-10\,\mathrm{Gpc}^{-3}\mathrm{yr}^{-1}\) at \(z\approx 0\). The rates at low redshifts may be significantly higher if young massive star clusters host IMBHs. The merger rates are dominated by IMBHs with masses between \(10^3-10^4\,\mathrm{M}_{\odot}\). Currently there are no LIGO/VIRGO upper limits for GW sources in this mass range, but our results show that at design sensitivity these instruments may detect these IMBH-SBH mergers in the coming years. LISA and the Einstein Telescope will be best suited to detect these GW events. The inspirals of IMBH-SBH systems may also generate an unresolved GW background.