SPECIAL ISSUES: BIOTECH
April 16, 2001
European Reaction Requires New Ways of Evaluating Risks and
Benefits of GMOs
By Carl Nelson, associate professor of production economics in the
Department of Agricultural and Consumer Economics at the University
of Illinois.
Genetic alteration of plants and animals is seen by many as an
interference with nature that has unknown and potentially disastrous
interactions with human genetics and natural ecosystems. Many consumers
are extremely wary of health threats caused by unknown risks in
food supply. Environmentalists have raised several questions about
the environmental risks of genetically altered crops and animals.
Environmental risks include the evolution of genetically modified
organisms (GMOs) into "super weeds," cross-pollination
introducing herbicide resistance into existing weeds or introducing
undesirable genetic traits into neighboring crops, and harm to non-target
populations caused by toxins introduced to create insect resistance.
In the United States, genetically altered corn and soybeans entered
the feed and food system without public concern. The transgenic
crops entered standard grain supply channels and substituted for
traditional crops in the production of a wide variety of food products
and animal feeds. To date, public concern about GMOs appears to
be limited to a small number of interest groups in the United States.
In contrast, Europe has imposed strong, restrictive regulations
on all transgenic crops in any portion of the food supply system.
This complex set of legislation and regulation is a response to
consumer demand for protection from the perceived harms that could
be caused by GMOs. England has seen multiple incidents of protestors
damaging GMO test fields. And French consumers have expressed extreme
mistrust of "contaminants" in the food supply. The result
is that European regulation of GMOs aims at reducing or eliminating
risks in the food supply, even if there is not strong scientific
evidence of such risks.
European regulation of GMOs has adopted the precautionary principle,
which directs that actions should be taken to prevent potential
harms even if there is a lack of scientific certainty about the
harm. The European Commission used this principle to freeze approval
of genetically altered maize that was related to the variety reported
to harm Monarch butterflies. When consumers perceive future dangers
that are highly uncertain, they are likely to prefer that regulatory
policies follow the precautionary principle. To overcome this caution
significant present benefits need to be visible.
The lessons of the European reaction to GMOs warn that these new
food products will be evaluated differently than traditional food
products. The uncertainties of the scientific manipulation of genetic
material are unfamiliar to the public. Under those circumstances,
extreme consumer reaction could be triggered at any time by a significant
public event.
Such a reaction could color the public evaluation of all GMOs,
as is apparently happening in Europe. To give each new product a
fair public evaluation, there needs to be a review process that
accounts for public perceptions and values, taking seriously the
obstacles for consumers to properly evaluate the costs and benefits
of new GMO products.
Public evaluation of GMOs that considers costs and benefits, while
giving strong preference to the protection of public health, is
needed to create a process to build trust. This process must acknowledge
the public perception on the part of some that GMOs are different
than conventional food products.
A number of consumers, especially in Europe, have already divided
food choices into non-GMO, and GMO. They will not be receptive to
arguments that GMOs are just modified forms of non-GMO food. They
will view GMOs as distinct products that require distinct review
and evaluation.
A review process with a strong commitment to the protection of
public health should include evaluation of the threats to public
health that would result from the failure to approve a GMO. Such
indirect effects that do not receive sensational press coverage
are the sorts of effects that need to be brought to public attention
through a credible public cost-benefit evaluation. What will build
trust is not so much explicit trust building, but changes in the
process that make the costs of single-minded better safe than
sorry' responses more visible.
The recommendations for credible public evaluation of GMOs aimed
at overcoming the obstacles to evaluation of costs and benefits
will require significant reallocation or new allocation of research
and regulatory expenditures. Failure to invest in the capacity to
conduct and communicate evaluations aimed at overcoming these obstacles
is likely to retard or halt the spread of social gains that researchers
expect to generate from GMOs.
The human tendency to see unknown, unfamiliar risks in an "all-or-nothing"
framework that places all emphasis on potential danger is strong
and pervasive. Unfounded assurances of safety, however, will not
help to move public opinion from "better safe, than sorry"
to an acceptable risk based on costs and benefits.
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