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We extend the parton‐hadron‐string dynamics (PHSD) transport approach in the partonic sector by explicitly calculating the total and differential partonic scattering cross sections as a function of temperature T and baryon chemical potential μB on the basis of the effective propagators and couplings from the dynamical quasiparticle model (DQPM) that is matched to reproduce the equation of state of the partonic system above the deconfinement temperature Tc from lattice quantum chromodynamics (QCD). We calculate the collisional widths for the partonic degrees of freedom at finite T and μB in the time‐like sector and conclude that the quasiparticle limit holds sufficiently well. Furthermore, the ratio of shear viscosity η over entropy density s, that is, η/s, is evaluated using the collisional widths and compared to lattice QCD(lQCD) calculations for μB = 0 as well. We find that the ratio η/s does not differ very much from that calculated within the original DQPM on the basis of the Kubo formalism. Furthermore, there is only a very modest change of η/s with the baryon chemical μB as a function of the scaled temperature T/Tc(μB). This also holds for a variety of hadronic observables from central A + A collisions in the energy range 5 GeV urn:x-wiley:00046337:media:asna201913708:asna201913708-math-0001 200 GeV when implementing the differential cross sections into the PHSD approach. Accordingly, it will be difficult to extract finite μB signals from the partonic dynamics based on “bulk” observables.
The biological effects of energetic heavy ions are attracting increasing interest for their applications in cancer therapy and protection against space radiation. The cascade of events leading to cell death or late effects starts from stochastic energy deposition on the nanometer scale and the corresponding lesions in biological molecules, primarily DNA. We have developed experimental techniques to visualize DNA nanolesions induced by heavy ions. Nanolesions appear in cells as “streaks” which can be visualized by using different DNA repair markers. We have studied the kinetics of repair of these “streaks” also with respect to the chromatin conformation. Initial steps in the modeling of the energy deposition patterns at the micrometer and nanometer scale were made with MCHIT and TRAX models, respectively.