No Arabic abstract
CREME96 and GEANT4 are two well known particle transport codes through matter in space science. We present a comparison between the proton fluxes outgoing from an aluminium target, obtained by using both tools. The primary proton flux is obtained by CREME96 only, covering an energy range from MeV to hundreds GeV with the same result in both cases. We studied different thickness targets and two different GEANT4 physics lists in order to show how the spectra of the outgoing proton fluxes are modified. Our findings show consistent agreement of simulation data by each tool, with regards both GEANT4 physics lists and every thickness target analysed.
A R&D project, named Nano5, has been recently launched to study an architectural design in view of addressing new experimental issues related to particle transport in high energy physics and other related physics disciplines with Geant4. In this frame, the first step has involved the redesign of the photon interaction models currently available in Geant4; this task has motivated a thorough investigation of the physics and computational features of these models, whose first results are presented here.
We present a precise measurement of downward-going albedo proton fluxes for kinetic energy above $sim$ 70 MeV performed by the PAMELA experiment at an altitude between 350 and 610 km. On the basis of a trajectory tracing simulation, the analyzed protons were classified into quasi-trapped, concentrating in the magnetic equatorial region, and un-trapped spreading over all latitudes, including both short-lived (precipitating) and long-lived (pseudo-trapped) components. In addition, features of the penumbra region around the geomagnetic cutoff were investigated in detail. PAMELA results significantly improve the characterization of the high energy albedo proton populations at low Earth orbits.
The Geant4-DNA project proposes to develop an open-source simulation software based and fully included in the general-purpose Geant4 Monte Carlo simulation toolkit. The main objective of this software is to simulate biological damages induced by ionising radiation at the cellular and sub-cellular scale. This project was originally initiated by the European Space Agency for the prediction of deleterious effects of radiation that may affect astronauts during future long duration space exploration missions. In this paper, the Geant4-DNA collaboration presents an overview of the whole ongoing project, including its most recent developments already available in the last Geant4 public release (9.3 BETA), as well as an illustration example simulating the direct irradiation of a chromatin fibre. Expected extensions involving several research domains, such as particle physics, chemistry and cellular and molecular biology, within a fully interdiciplinary activity of the Geant4 collaboration are also discussed.
As simulation system, the variety of physics processes implemented is one of the most important functionalities. In that sense, Geant4 is one of the most powerful simulation toolkits. Its flexibility and expansibility brought by object-oriented approach make it possible for us to easily assimilate external simulation packages into the Geant4 system as modules of physics processes. We developed an interface for using EGS4, which is another of the most well-known simulation package for electromagnetic physics, in Geant4. By means of this interface, EGS4 users can share Geant4 powerful resources, such as geometry, tracking, etc. It is also important that it can provide a common environment for comparison tests between EGS4 and Geant4. In this paper, we describe our design and implementation of the interface.
The Geant4 reference paper published in Nuclear Instruments and Methods A in 2003 has become the most cited publication in the whole Nuclear Science and Technology category of Thomson-Reuters Journal Citation Reports. It is currently the second most cited article among the publications authored by two major research institutes, CERN and INFN. An overview of Geant4 presence (and absence) in scholarly literature is presented; the patterns of Geant4 citations are quantitatively examined and discussed.