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Notes: Abstract Photoproton spectra have been obtained from gaseous18O,20Ne,22Ne,36Ar,40Ar,84Kr, Kr and Xe and from foils of23Na and K irradiated with bremsstrahlung from 24 to 32.5 MeV endpoint energy. The charged particles have been detected at 90° to theγ-beam by a Cs I(Tl)-spectrometer with pulse shape discrimination. Yields and lower limits for the integrated cross sections are given. For argon and the heavier nuclei, the results are compared with statistical-model calculations.

Notes: Abstract K-, L- andM-x ray production cross sections for the molecular excitation regime in heavy ion-atom collisions (Z 1+Z 2≧100) are reported for the projectile velocity range 1.3–3.7 a.u. Outer-shell vacancy configurations of the collision partners having experienced inner shell vacancy creating collisions are deduced from the x-ray spectra. The influence of outer shell vacancy occupation on fluorescence yields is discussed and vacancy production cross sections are derived from x-ray production cross sections.

Notes: Abstract The energy spectrum of photoprotons from4He was investigated with 28 and 32,5 MeV bremsstrahlung using a CsI(Tl)-spectrometer and a Si-counter. The (γp)-cross section was derived for excitation energies from 23 to 32 MeV.

Notes: Abstract The velocity of the quasimolecular x-ray emitter is found via Doppler shift measurements. It is in agreement with the center of mass velocity. Applying Doppler shift corrections the intrinsic anisotropy of the quasi-molecularM radiation is determined as a function of x-ray energy for 6 to 45 MeV I bombardment on thin Au targets. Position and amplitude of the maximum anisotropy in the x-ray spectrum depend on impact energy.

Notes: Summary X- and gamma-irradiation of human erythrocyte membranes (250–1000 Gy) was found to decrease the ratio of weakly to strongly immobilized signal height of membrane-bound maleimide spin label (Mal-6). Subsequent incubation of spin-labeled membranes at ambient temperature (21 °C) induced a progressive increase in this ratio, faster for membranes irradiated with low doses which was hampered by protease inhibitors. These results demonstrate that ionizing radiation stimulates proteolysis of erythrocyte membrane proteins by membrane-associated proteases.

Notes: Summary Swift heavy ions when penetrating through matter strip off those electrons having a smaller orbital velocity than the ion velocity. The remaining electrons screen the nuclear charge yielding an effective charge. The effective charge of the ions interacts predominately with the target electrons causing excitation and ionizations of the target atoms. Using the Bethe Bloch formula for the energy loss combined with the Barkas formula for effective charge, the energy loss values as well as unrestricted and restricted linear transfer can be calculated within a few percent of accurancy. From the primary energy loss only a small fraction of 10% or less is transformed into excitation. The major part of the energy loss is used for the ionization of the target atoms and the emission of the corresponding electrons with a high kinetic energy. These electrons form the track around the trajectory of the primary ion in which two thirds of the primary energy is deposited by collisions of primary, secondary and later generations of electrons with the target molecules. In the electron diffusion process the energy is transported from the center of the track into the halo. The radial dose decreases with the square of the radial distance from the center. The diameter of the track is determined by the maximum range of the emitted electrons, i.e. by the maximum energy electrons. All ions having the same velocity i.e. the same specific energy produce electrons of the same energy and therefore tracks of the same diameters independent of the effective charge. But the dose inside the track increases with the square of the effective charge. Track structure models using this continuous dose distributions produce a better agreement with the experiment than models based on microdosimetry. The critical volume as used in microdosimetry is too large compared to the size of the DNA as critical structure inside the biological objects. Track structure models yield better results because the gross-structure of the track i.e. its lateral extension and the thin down toward the end of the track is included in these calculations. In a recent refinement the repair capacity of the cell has been included in a track structure model by using the complete shouldered x-ray survival curve as a template for the local damage produced by the particle tracks. This improved model yields presently the best agreement with the experiment.

Notes: Abstract An experimental setup using static-field gel electrophoresis (SFGE) was developed to determine radiation-induced DNA double-strand breaks (DSBs) in CHO-K1 cells after exposure to X-rays or heavy charged particles. The fraction of DNA eluted into the gel matrix depends on the quantity of DSBs introduced. In agreement with a recent report, SFGE and pulsed-field electrophoresis were found to be equally sensitive in DSB detection. With radiolabeled DNA from cell cultures, the absolute amount of DNA migrating out of agarose plugs into the gel was quantified by determining the radioactivity in the gel lane. Alternatively, relative measurements of the amount of DNA released into the gel were achieved with a standardized protocol for both SFGE and a subsequent densitometric scanning of photographic negatives from gels stained with ethidium bromide. After calibration with the radioactive method, the fractions of DNA retained could be calculated directly from the data obtained with the densitometric assay to set up classical dose-effect curves. This procedure was validated for its application with heavy ions using an 500 MeV/u lead beam.

Notes: Abstract Human erythrocytes were irradiated with heavy ions of energies between 4 and 18 MeV/u having linear energy transfer (LET) values between 92 and 14000 keV/µm. Hemolysis has been studied as a macroscopic parameter for membrane damage and changes of the fluidity as a more microscopic parameter. The membrane fluidity changed in a characteristic dose-dependent manner as detected by electron spin resonance employing 12-doxylstearic acid methyl ester spin label (SL 12). Lysis cross sections and RBE values were determined from dose effect curves. The results demonstrate a high hemolytic efficiency of heavy ions compared to X rays. With increasing LET values the measured relative biological efficiency (RBE) values increase continuously. In the complete LET range the cross sections formed one common curve as function of LET and no saturation effects are observed. This is in direct contrast to other biological endpoints such as cell inactivation or DNA damage.

Notes: Abstract A Monte Carlo model is presented to study details of the energy deposition inside tracks of heavy charged particles in water vapor. The input data for most of the calculations based on the binary encounter approximation are double-differential cross sections for electron emission after heavy-ion impact. The paths of the liberated electrons are simulated, taking into account elastic scattering, ionization, and excitation. Each basic interaction of an electron or heavy ion is treated individually. Radial dose distributions and specific energy deposition are calculated for projectiles from protons to uranium in the energy range from one to several hundred megaelectron volts per unified atomic mass unit. Good agreement with measurements in tissue-equivalent gas and propane is obtained for light and medium-heavy projectiles, whereas for heavy projectiles such as uranium, deviations around a factor of 2–3 are observed.