RESUMEN
More than a decade has passed since a complete revision was initiated of the radiation doses received by survivors of the Hiroshima and Nagasaki atomic bombings. The new dosimetry system (DS86) was completed in 1986 and adopted shortly thereafter. Overall, DS86 was noted to be a clear improvement over the old dosimetry system. However, based on limited validation measurements, troublesome inconsistencies were suggested for neutrons. Since 1986, a substantial number of additional neutron activation measurements have been made in mineral and metal samples from Hiroshima. Importantly, a large number of measurements have now been made at distances beyond 1 km. Here, inconsistencies between neutron activation measurements and DS86 calculations for Hiroshima are examined using all available measurement data, including new measurements for 36Cl which extend the measurement range to more than 1.7 km from the epicenter, and Monte Carlo modeling calculations for each sample measured. Results show that thermal neutron activation measured beyond approximately 1 km in Hiroshima (at distances most relevant for radiation-risk evaluation) is two to 10, or more, times higher than that calculated based on DS86. Similar trends observed when comparing results by several independent measurement laboratories, using different analytical methods, suggest that the DS86 calculations for low-energy neutrons are in error. Because of the importance of the Hiroshima data in radiation risk evaluation, this large discrepancy is in need of resolution.
Asunto(s)
Neutrones , Japón , Fenómenos Físicos , Física , RadiometríaRESUMEN
Measurements have been made of the ratios of chlorine-36 to chlorine in five halite samples from Searles Lake sediments, previously dated by carbon-14, thorium-230, and magnetostratigraphic techniques. The ages calculated from the chlorine ratios are generally concordant with those from the other methods, implying the constancy of the chlorine input ratio over the last million years.
RESUMEN
The recently developed direct counting technique for radiocarbon atoms has been used to measure the relative numbers of such atoms in various geological samples which had earlier been dated by the beta-ray counting method. Sample weights ranged from 3.5 to 15 milligrams. The dates determined by the two methods are consistent with each other. Further experience with the new method is also reported.
RESUMEN
Mass spectrometric methods have long been suggested as ways of measuring (14)C/(12)C ratios for carbon dating. One problem has been to distinguish between (14)N and (14)C. With negative ions and a tandem electrostatic accelerator, the (14)N background is virtually absent and fewer than three (14)C atoms in 10(16) atoms of (12)C have been easily measured.