Analysis of secondary electron emission spectra of equal-LET protons and alpha particles for purposes of radiation quality and spaceflight hazard assessment.

Amongst the great variety of heavy particles present in the galactic and solar cosmic ray spectra, hydrogen and helium nuclei are significantly more abundant than all other heavier ions and, as such, represent a major radiation hazard to humans in space. Experimental data have suggested that differences in relative biological effectiveness (RBE) exist between the two species at the same value of linear energy transfer (LET). This has consequences for heavily ionising radiation protection procedures, which currently still assume a simple dependence of radiation quality on LET. By analysing the secondary electron (delta-ray) emission spectra of protons and alpha particles, in terms of the spatial characteristics of energy deposition in cellular targets and the likelihood of complex lesion formation, a numerical quantity representing biological effectiveness is generated. When expressed relative to a reference radiation, this quantity is found to differ for protons and a particles of the same LET, demonstrating not only the ion-specific nature of RBE but also the inadequacy of specifying radiation quality as a function of LET only. Such a method for numerically assessing radiation quality may have implications for procedures for heavy ion protection in space at low doses and for understanding the initial mechanisms of radiation action.

An assessment of galactic cosmic radiation quality considering heavy ion track structures within the cellular environment.

Beyond the magnetic influence of the Earth, the flux of galactic cosmic radiation (GCR) represents a radiological concern for long-term manned space missions. Current concepts of radiation quality and equivalent dose are inadequate for accurately specifying the relative biological "efficiency" of low doses of such heavily ionising radiations, based as they are on the single parameter of Linear Energy Transfer (LET). Such methods take no account of the mechanisms, nor of the highly inhomogeneous spatial structure, of energy deposition in radiation tracks. DNA damage in the cell nucleus, which ultimately leads to the death or transformation of the cell, is usually initiated by electrons liberated from surrounding molecules by the incident projectile ion. The characteristics of these emitted "delta-rays", dependent primarily upon the charge and velocity of the ion, are considered in relation to an idealised representation of the cellular environment. Theoretically calculated delta-ray energy spectra are multiplied by a series of weighting algorithms designed to represent the potential for DNA insult in this environment, both in terms of the quantity and quality of damage. By evaluating the resulting curves, and taking into account the energy spectra of heavy ions in space, a relative measure of the biological relevance of the most abundant GCR species is obtained, behind several shielding configurations. It is hoped that this method of assessing the radiation quality of galactic cosmic rays will be of value when considering the safety of long-term manned space missions.

Fluxes of galactic iron nuclei and associated HZE secondaries, and resulting radiation doses, in the brain of an astronaut.

Although galactic iron nuclei constitute only a small percentage of the total flux of radiation in space, they are extremely significant from a biological standpoint, and represent a concern for long-term manned space missions of the future. Dosages resulting from iron nuclei, and the high-charge secondary nuclei subsequently produced in nuclear fragmentation reactions, have been calculated at the centre of a simple model of the human brain, shielded by various thicknesses of aluminium. Three mission scenarios are considered representing different geomagnetic shielding conditions at solar minimum. Without artificial shielding absorbed dose rates outside the magnetosphere, in polar orbit and in the proposed Space Station orbit, are approximately 0.3, 0.1 and 0.03 cGy/year respectively, corresponding to dose equivalent rates of 8.0, 2.5 and 0.8 cSv/year, and decreasing by roughly a factor of two behind 10 g/cm2 of aluminium. In line with new approaches to risk estimation based on particle fluence and track structure, calculations of the number of cell nuclei likely to be struck by these HZE particles are also presented. Behind 10 g/cm2 of aluminium, 3.4%, 1.3% and 0.5% of cell nuclei at the centre of the brain will be traversed at least once by such a particle within three years, for the three mission scenarios respectively.