-Caveat Lector-

United States Senate Testimony before the Committee on Veterans' Affairs
May 6, 1994
Open Air Testing with Simulated Biological and Chemical Warfare Agents

By Leonard A. Cole, Ph.D.
My name is Leonard A. Cole, and I teach science and public policy at
Rutgers University in Newark. My research interests include biological and
chemical warfare policies, and I have written in particular about testing
done in the U.S Army's biological defense program.
I appreciate your invitation, Senator Rockefeller, to testify about
experiments involving simulated biological and chemical warfare agents.
These agents, which the army calls simulants, are intended to mimic more
lethal bacteria and chemicals that might be used in actual warfare.
As described in my book, Clouds of Secrecy, the army began a program in
1949 to assess the nation's vulnerability to attack with biological
weapons. During the next 20 years, the army released simulant agents over
hundreds of populated areas around the country. Targets included portions
of Hawaii and Alaska, San Francisco, St. Louis, Minneapolis, New York City,
Washington, D.C., Key West, and many other cities. The purpose was to see
how the bacteria spread and survived as people went about their normal
activities.
Evidence suggested that the tests may have been causing illness to exposed
citizens. Nevertheless, as army spokesmen subsequently testified, the
health of the millions of people exposed was never monitored because the
army assumed that the bacteria and chemicals were harmless.
Vulnerability testing continues at Dugway Proving Ground, 70 miles from
Salt Lake City. Several smaller communities are closer to the base, and
Dugway itself is home to hundreds of civilians and military personnel and
their families. The stated purpose of the tests is to evaluate biological
detector systems and protective gear.
Since tests involve spraying simulants outdoors, it is important to
understand how much risk they pose to humans who are exposed. Official
statements have not always been dear on this matter. A July 1993 news
release by the Dugway Public Affairs Office indicates that "no specific
safety controls or protection are required for testing with simulants." The
statement implies, erroneously, that the simulants are harmless.
In fact, during 45 years of open air testing, from time to time the army
has stopped using certain simulants for reasons of safety. In each instance
the army belatedly recognized they could be causing disease and death,
although such information had long been available in the medical
literature. This was the case in the 1950s when it ceased using the fungus
Aspergillus fumigatus as a simulant. The fungus had long been known to
cause aspergillosis, a disease that can be fatal. Similarly, in the 1960s
the army stopped using zinc cadmium sulfide, a chemical that had been known
for years to cause cancer.
In the 1970s, the bacterium Serratia marcescens, a source of infections
that can lead to death, was taken out of service as a simulant. And in the
1980s, dimethyl methylphosphonate, a chemical known as DPP, was removed
from use as a simulant because of its carcinogenic and other toxic
potential. I understand that one of today's witnesses, Earl Davenport, was
exposed to DMMP at Dugway in 1984 and may still be suffering health
problems as a result.
Indeed, simulants now used at Dugway continue to pose risks. The chemical
ethylene oxide, which is present in some of the mixtures used in outdoor
spraying, is a known carcinogen. The bacterium Bacillus subtilis, while not
generally seen as dangerous, is cited in medical textbooks as able to cause
serious infections. In truth any microorganism that seems harmless under
some circumstances may cause illness under others.
Exposure to high concentrations of any microorganism can be critically
dangerous to people in weakened conditions. The elderly, the very young,
people with AIDS and others who have weakened immune systems are more
susceptible to life threatening infections. Nevertheless, the army has not
monitored the health of citizens who may have been exposed during its tests
while maintaining that its bacterial agents cause no harm.
In addition to people who are unwittingly exposed to the army's bacteria
and chemicals, human research subjects may not be receiving appropriate
information. A test at Dugway in November 1993, for example, raises
important questions in this regard. The test was intended to assess the
ability of chemical agents to penetrate protective clothing.
Test subjects wore special outer garments and were then sprayed with
chemicals in simulated battle conditions. An army Environmental Assessment
before the test indicated that some of the chemicals could be toxic. Yet
the consent form that the subjects signed in advance of the test said
nothing about any of the chemicals.
Subsequently, two of the test subjects said they were asked to sign another
consent form sometime after the test had been completed. The second form
described the chemicals. But having the subjects sign a consent form after
an experiment, rather than before, makes little ethical sense. The
procedure renders meaningless the notion of informed consent.
Finally, several physicians at the University of Utah Medical School in
Salt Lake City continue to express concern about the tests at Dugway. They
do not feel they have information that would enable them optimally to
handle infections and complications that might be caused by the tests.
Dugway officials have thus far not satisfied their concerns either about
field tests involving simulants or indoor tests with highly pathogenic
agents.
These are a few of the disconcerting issues associated with testing at
Dugway. If such tests must continue, several policy suggestions seem
appropriate:
--Inform people in the area before each test that they may be exposed to
the army's biological and chemical agents.
--For a substantial period after each test, monitor the health of the
exposed population.
--Provide comprehensive information in understandable language to human
subjects before they participate in any test.
--Fully inform the neighboring medical community about the nature of each
test and its possible medical complications.
--Above all, strive for safety, candor, and openness.

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