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Re: EPA, risk and dose
Eric,
Your explanation below makes sense, because that amounts to choosing a
different set of units to express the limits, but that does not jive with
the
EPA written guidance, which states, e.g., "No simple and direct conversion
between radiation dose and radiogenic cancer risk is available...a given
dose
from one radionuclide via a given exposure pathway may present a much
greater cancer risk than the same dose from another radionuclide and/or
exposure pathway...Therefore, any conversion between dose and risk must be
performed on a radionuclide-and pathway-specific basis."
It seems to me, they are saying that the energy imparted to a given organ by
one radionuclide being inhaled will not have the same effect as the same
total energy imparted to the same organ by a different radionuclide that is
ingested. And, that's where they lose me. The different effects of
high-LET
vs. low-LET radiation are built in via the quality factors to dose
calculations, so that does not help the EPA's argument any.
If, instead, they are meaning to say that a different pathway and/or
different
radionuclide will impact different organs, that doesn't help their argument
either, because that information also goes into the dose calculations.
Finally, they may be saying, without ever saying it, that the NRC's use of
the
CEDE does not adequately characterize the overall cancer risk, because the
ICRP's normalization of the doses and effects is inadequate, but their own
guidance contradicts that
possibility.
The only thing they can possibly be saying is that 100 rem to the thyroid
from
the inhalation of I-131 will not create the same risk of cancer as 100 rem
to
the thyroid from the ingestion of I-125, and that means they have some
other
idea about just what is causing the damage and/or risk.
Barbara L. Hamrick
BLHamrick@aol.com
In a message dated Thu, 29 Mar 2001 12:54:44 PM Eastern Standard Time,
"Frohmberg, Eric"
<Eric.Frohmberg@STATE.ME.US> writes:
<< As I understand it, EPA's cancer slope factor has all the dosimetry
assumptions built into it. There are some differences in the dosimetry
(which version of ICRP is used, etc.), but instead of taking an intake
(pCi/lifetime) and calculating a dose, they are simply calculating risk.
And, of course, the risk estimates would change over time just as the dose
estimates would.>>
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