Food
First Special Report no. 1
Genetic Engineering in Agriculture: The Myths, Environmental Risks,
and Alternatives
Miguel
A. Altieri
University of California, Berkeley
Food
First/Institute for Food and Development Policy
Oakland, California
Copyright
⌐ 2000 Institute for Food and Development Policy. All rights
reserved. No part of this book may be reproduced or transmitted in
any form or by any means, electronic or mechanical, including photocopying,
recording or by any information storage retrieval system, without
written permission from the publisher, except for brief review.
Text
and cover design by
Food First Books
398 60th
Street
Oakland, California 94618
www.foodfirst.org
Library
of Congress Cataloging-in-Publication Data
Food
First Books are distributed by:
LPC Group
1436 West Randolph Street
Chicago, IL 60607
(800) 243-0138
www.coolbooks.com
Printed
in the United States of America
Background
Until
about four decades ago, crop yields in US agriculture depended on
internal resources, recycling of organic matter, built-in biological
control mechanisms, and rainfall patterns. Agricultural yields were
modest, but stable. Production was safeguarded by growing more than
one crop or variety in space and time in a field as insurance against
pest outbreaks or severe weather. Nitrogen was replaced in the soil
by rotating major field crops with legumes. Rotations suppressed insects,
weeds, and diseases by effectively breaking the life cycles of these
pests. A typical Corn Belt farmer grew corn in rotation with several
crops, including soybeans, and small grain production was intrinsic
to maintain livestock. Most of the labor was done by the family who
owned the farm, with occasional hired help. No specialized equipment
or services were purchased from off-farm sources (Altieri 1995; Audirac
1997).
In
the developing world, small farmers developed even more complex and
biodiverse farming systems, guided by indigenous knowledge that has
stood the test of time (Thrupp 1998). In this type of farming, the
link between agriculture and ecology was quite strong and signs of
environmental degradation were seldom evident.
But
as agricultural modernization progressed, the ecology-farming linkage
was often broken as ecological principles were ignored and/or overridden.
Profit, rather than people╞s needs or environmental concerns,
has shaped agricultural production. Agribusiness interests and prevailing
policies favored large farm size, specialized production, crop monocultures,
and mechanization.
Today
monocultures have increased dramatically worldwide, mainly through
the geographical expansion of land annually devoted to single crops.
Monoculture has implied the simplification of biodiversity, the end
result being an artificial ecosystem requiring constant human intervention
in the form of agrochemical inputs, which, in addition to temporarily
boosting yields, result in a number of undesirable environmental and
social costs. Aware of such impacts, several agricultural scientists
have arrived at a general consensus that modern agriculture confronts
an ecological crisis (Conway and Pretty 1991).
The
yearly loss of yields due to pests in many crops (reaching about 30
percent in most crops), despite the substantial increase in the use
of pesticides (about 500 million kg of active ingredient worldwide)
is a symptom of the environmental crisis affecting agriculture. Cultivated
plants grown in genetically homogenous monocultures do not possess
the necessary ecological defense mechanisms to tolerate the impact
of outbreaking pest populations (Altieri 1994).
When
these agricultural models were exported to Third World countries through
the so-called Green Revolution, environmental and social problems
were exacerbated. Most resource-poor farmers of Latin America, Asia,
and Africa gained very little from the process of development and
technology transfer of the Green Revolution, as proposed technologies
were not scale-neutral. Farmers with the larger and better-endowed
lands gained the most, but farmers with fewer resources and located
in marginal environments often lost, and income disparities were often
accentuated (Conway 1997).
Technological
change has mainly favored the production of export and/or commercial
crops produced primarily in the large farm sector, with a marginal
impact on productivity of crops for food security, which are largely
grown by the peasant sector (Pretty 1995). In areas where conversion
from subsistence to a cash agricultural economy progressively occurred,
a number of ecological and social problems became evident: loss of
food self-sufficiency, genetic erosion, loss of biodiversity and traditional
farming knowledge, and permanence of rural poverty (Conroy et al.
1996).
In
order to sustain such agro-export systems, many developing countries
have become net importers of chemical inputs and agricultural machinery,
increasing government expenditures and exacerbating technological
dependence. For example, between 1980 and 1984, Latin America imported
about US $430 million worth of pesticides and used about 6.5 million
tons of fertilizers (Nicholls and Altieri 1997). Such massive use
of agrochemicals led to a major environmental crisis of yet unmeasured
social and economic proportions.
What
is ironic is the fact that the same economic interests that promoted
the first wave of agrochemically-based agriculture, are now celebrating
and promoting the emergence of biotechnology as the latest ⌠magic
bullet.÷ Biotechnology, they say, will revolutionize agriculture with
products based on nature╞s own methods, making farming more
environmentally friendly and more profitable for farmers and healthy
and nutritious to consumers (Hobbelink 1991).
The
global fight for market share is leading major corporations to massively
deploy genetically engineered plants (transgenic crops) around the
world (more than 40 million hectares in 1999) without proper advance
testing of short or long term impacts on human health and ecosystems.
This expansion has been helped along by marketing and distribution
agreements entered into by corporations and marketers (i.e. Ciba Seeds
with Growmark and Mycogen Plant Sciences with Cargill), and in the
absence of regulations in many developing countries.
In
the US, the policies of the Food and Drug Administration (FDA) and
Environmental Protection Agency (EPA) consider genetically modified
crops to be ⌠substantially equivalent÷ to conventional crops.
These policies have been developed in the context of a regulatory
framework that is inadequate and, in some cases, completely absent.
The
agrochemical corporations who increasingly control the direction and
goals of agricultural innovation claim that genetic engineering will
enhance the sustainability of agriculture by solving the very problems
affecting conventional farming, and will spare the Third World from
low productivity, poverty, and hunger.
By matching
myth with reality, the objective of this book is to challenge the
false promises made by the genetic engineering industry. They have
promised that genetically engineered crops will move agriculture away
from a dependence on chemical inputs, increase productivity, decrease
input costs, and help reduce environmental problems (Office of Technology
Assessment 1992). By challenging the myths of biotechnology, we expose
genetic engineering for what it really is: another technological fix
or ⌠magic bullet÷ aimed at circumventing the environmental problems
of agriculture (which are the outcome of an earlier round of technological
fix) without questioning the flawed assumptions that gave rise to
the problems in the first place (Hindmarsh 1991). Biotechnology promotes
single-gene solutions for problems derived from ecologically unstable
monoculture systems designed on industrial models of efficiency. Such
a unilateral and reductionist approach has already proven ecologically
unsound in the case of pesticides, which also espoused a reductionist
approach, using one chemical√one pest as opposed to the one
gene√one pest approach now promoted by biotechnology (Pimentel
et al. 1992).
Modern
industrial agriculture, today epitomized by biotechnology, is founded
on a philosophical premise that is fundamentally flawed. It is precisely
this premise that needs to be exposed and criticized in order to advance
towards a truly sustainable agriculture. This is particularly relevant
in the case of biotechnology, where the alliance of reductionist science
and multinational monopolistic industry will take agriculture further
down a misguided road. Biotechnology perceives agricultural problems
as genetic deficiencies of organisms and treats nature as a commodity,
while in the process making farmers more dependent on an agribusiness
sector that increasingly concentrates power over the food system.
Biotechnology,
World Hunger, and the Welfare of Farmers
Hungry
people in the midst of plenty
Biotechnology
companies often claim that genetically modified organisms (GMOs)∙specifically
genetically altered seeds∙are essential scientific breakthroughs
needed to feed the world and reduce poverty in developing countries.
Most international organizations charged with policies and research
to enhance food security in the developing world echo this view. This
view rests on two critical assumptions: that hunger is due to a gap
between food production and human population density or growth rate;
and that genetic engineering is the only or best way to increase agricultural
production and so meet future food needs.
A
starting point to clarify these misconceptions is to understand that
there is no relationship between the prevalence of hunger in a given
country and its population. For every densely populated and hungry
nation like Bangladesh or Haiti, there is a sparsely populated and
hungry nation like Brazil and Indonesia. The world today produces
more food per inhabitant than ever before. Enough food is available
to provide 4.3 pounds for every person every day: 2.5 pounds of grain,
beans, and nuts, about a pound of meat, milk, and eggs, and another
of fruits and vegetables (LappΘ et al. 1998).
In
1999 enough grain was produced globally to feed a population of eight
billion people (six billion inhabit the planet in 2000) had it been
evenly distributed or not fed to animals. Seven out of 10 pounds of
grain are fed to animals in the US. Countries such as Brazil, Paraguay,
Thailand, and Indonesia devote thousands of acres of agricultural
land to produce soybeans and manioc for export to feed cattle in Europe.
By channeling one third of the grain produced worldwide to needy people,
hunger would cease instantly (LappΘ et al. 1998).
Hunger
is also compounded by globalization, especially when developing countries
embraces the free trade policies advocated by international lending
agencies (lowering tariffs and allowing goods from industrialized
countries to flow in). The experience of Haiti, one of the world╞s
poorest countries is illuminating. In 1986 Haiti imported just 7,000
tons of rice, with the majority being grown on the island. After opening
its economy to the world, cheaper rice immediately flooded in from
the US, where the rice industry is subsidized. By 1996 Haiti imported
196,000 tons of foreign rice at the cost of US $100 million a year.
Haitian rice production became negligible once the dependence on foreign
rice was complete. The cost of rice rose, leaving large numbers of
poor people at the whim of rising world grain prices. Hunger increased
(Aristide 2000).
The
real causes of hunger are poverty, inequality, and lack of access
to food and land. Too many people are too poor (about two billion
survive on less than one dollar a day) to buy the food that is available
(but often poorly distributed) or lack the land and resources to grow
it themselves (LappΘ et al. 1998). Because the true root cause
of hunger is inequality, any method of boosting food production that
deepens inequality will fail to reduce hunger. Conversely, only technologies
that have positive effects on the distribution of wealth, income,
and assets, that are pro-poor, can truly reduce hunger. Fortunately,
such technologies do exist, and can be loosely grouped together under
the discipline of agroecology, the potential of which has been amply
demonstrated and later in this book analyzed more fully (Altieri et
al. 1998; Uphoff and Altieri 1999).
Attacking
inequality head-on by true land reform holds the promise of productivity
gains far outweighing the potential of agricultural biotechnology.
While industry proponents will often hold out the promise of 15 percent,
20 percent, or even 30 percent yield gains from biotechnology, smaller
farms today produce from 200 to 1,000 percent more per unit area than
larger farms worldwide (Rosset 1999). Land reforms that bring average
land holdings down to their optimum (small) size, from the inefficient,
unproductive overly large units that characterize much of world agriculture
today, could provide the basis for production increases, beside which
the much ballyhooed promise of biotechnology would pale in comparison.
It
is critical to understand that most innovations in agricultural biotechnology
have been profit-driven rather than need-driven. The real thrust of
the genetic engineering industry is not to make agriculture more productive,
but rather to generate profits (Busch et al. 1990). This is illustrated
by reviewing the principle technologies on the market today: (1) herbicide
resistant crops, such as Monsanto╞s ⌠Roundup Ready÷ soybeans,
seeds that are tolerant to Monsanto╞s herbicide Roundup, and
(2) ⌠Bt÷ (Bacillus thuringiensis) crops which are engineered
to produce their own insecticide. In the first instance, the goal
is to win greater herbicide market-share for a proprietary product
and, in the second to boost seed sales at the cost of damaging the
usefulness of a key pest management product (the Bt-based microbial
insecticide) relied upon by many farmers, including most organic farmers,
as a powerful alternative to insecticides.
These
technologies respond to the need of biotechnology companies to intensify
farmers╞ dependence upon seeds protected by so-called ⌠intellectual
property rights÷ which conflict directly with the age-old rights of
farmers to reproduce, share, or store seeds (Fowler and Mooney 1990).
Whenever possible, corporations require farmers to buy a company╞s
brand of inputs and forbid farmers from keeping or selling seed. In
the US farmers adopting transgenic soybeans must sign an agreement
with Monsanto. If they sow transgenic soybeans the next year, the
penalty is about $3,000/acre depending of the acreage. This fine could
cost farmers their farms, their livelihood. By controlling germplasm
from seed to sale, and by forcing farmers to pay inflated prices for
seed-chemical packages, companies are determined to extract the most
profit from their investment (Krimsky and Wrubel 1996).
What
about golden rice?
Scientists
that support biotechnology and disagree with the assertion that most
biotechnology research is profit- rather than need-driven, use the
newly developed but not yet commercialized golden rice to hide behind
a rhetoric of humanitarianism. This experimental rice is rich in beta
carotene, or Vitamin A precursor, which is an important nutrient to
millions of children, especially in Asia, that suffer from Vitamin
A deficiency, which can lead to blindness.
Developers
of the golden rice say that this new crop was developed with public
funds, and that once the rice proves viable in field plantings, it
will be freely distributed to the poor. The suggestion that genetically
altered rice is the proper way to address the condition of two million
children at risk of Vitamin A deficiency-induced blindness reveals
a tremendous naivetΘ about the reality and causes of vitamin
and micro-nutrient malnutrition. If one reflects upon the patterns
of human development and nutrition, one must quickly realize that
Vitamin A deficiency is not best characterized as a problem, but rather
as a symptom, a warning sign. It warns us of broader inadequacies
associated with both poverty, and with agricultural change from diverse
cropping systems toward rice monoculture promoted by the Green Revolution.
People
do not exhibit Vitamin A deficiency because rice contains too little
Vitamin A, or beta carotene, but rather because their diet has been
reduced to rice and almost nothing else, and they suffer from many
other dietary illnesses that cannot be addressed by beta carotene,
but which could be addressed, together with Vitamin A deficiency,
by a more varied diet. Golden rice must be seen as a one-dimensional
attempt to fix a problem created by the Green Revolution: the problem
of diminished crop and dietary diversity.
A
⌠magic bullet÷ solution, which places beta carotene into rice∙with
potential health and ecological hazards∙while leaving poverty,
poor diets, and extensive monoculture intact, is unlikely to make
any durable contribution to well-being. To use the words of Vandana
Shiva, ⌠such an approach reveals blindness to readily available
solutions to Vitamin A deficiency-induced blindness, including many
ubiquitous leafy plants which when introduced (or re-introduced) into
the diet provide both needed beta carotene and other missing vitamins
and micro-nutrients÷. Although wild green vegetables have been regarded
as peripheral to the peasant household, gathering as currently practiced
in many rural farming communities, affords a meaningful addition to
the peasant family nutrition and subsistence. Within and on the periphery
of paddy rice fields, there is an abundance of wild and cultivated
green leafy vegetables rich in vitamins and nutrients, most of which
are eliminated when farmers adopt monocultures and associated herbicides
(Greenland 1997).
Rice
biotechnologists have no understanding of the deeply rooted cultural
traditions that determine food preferences among Asian people, especially
the social and even religious significance of white rice. It is highly
unlikely that the golden rice will replace white rice, which for millennia
has played a variety of nutritional, culinary, and ceremonial roles.
There is no doubt that golden rice will bump into the traditions associated
with white rice, as green or blue French fries would bump into Western
food preferences in the US.
But
even if golden rice made it into the bowls of poor Asians, there is
no guarantee that it would benefit poor people that don╞t eat
fat-rich or oil-rich foods. Beta carotene is fat-soluble and its uptake
by the intestine depends upon fat or oil in the diet. Moreover, people
suffering protein-related malnutrition and lacking dietary fats and
oils cannot store Vitamin A well in the liver, nor transport it to
the different body tissues where the vitamin is needed. Given the
low concentration of beta carotene in the miracle rice, people would
have to eat more than one kilogram of rice per day to obtain a recommended
daily allowance dosage of Vitamin A.
Does
biotechnology increase yields?
A major
argument advanced by biotechnology proponents is that transgenic crops
is that they will significantly boost crop yields. These expectations
have been examined by a US Department of Agriculture (USDA) Economic
Research Service (ERS) report (1999), which analyzed data collected
in 1997 and 1998 for 12 and 18 US region/crop combinations, respectively.
The crops surveyed were Bt corn and cotton, and herbicide tolerant
(HT) corn, cotton, and soybeans, and their non-engineered counterparts.
In
1997, yields were not significantly different in engineered versus
non-engineered crops in seven of 12 crop/region combinations. Four
of 12 regions showed significant increases (13√21 percent) in
yield of engineered versus non-engineered crops (HT soybeans in three
regions and Bt cotton in one region). Herbicide tolerant cotton in
one region showed a significant reduction in yield (12 percent), compared
with its non-engineered counterparts.
In 1998, yields were not significantly different in engineered versus
non-engineered crops in 12 of 18 crop/region combinations. Five crop/region
combinations (Bt corn in two regions, HT corn in one region, Bt cotton
in two regions) showed significant increases in yield (five to 30
percent) of engineered over non-engineered crops, but only under high
pressure from the European corn borer, which is sporadic. Herbicide
tolerant cotton (glyphosate-tolerant) was the only engineered crop
that showed no significant increase in yield in either region where
it was surveyed.
In
1999 researchers at the University of Nebraska╞s Institute of
Agriculture and Natural Resources grew five different Monsanto soybean
varieties, together with their closest conventional relatives, and
the highest-yielding traditional varieties in four locations around
the state using both drylands and irrigated fields. On average, researchers
found the genetically engineered varieties∙though more expensive∙produced
six percent less than their non-genetically engineered near relatives,
and 11 percent less than the highest yielding conventional crops.
Reports from Argentina show the same non-yield enhancing results with
HT soybeans which universally seems to exhibit yield drag.
Yield
losses are amplified in crops, such as Bt corn, where it is mandatory
for farmers to leave 20 percent of their land as refuges made up of
non-transgenic corn. It is expected that patchworks of transgenic
and non-transgenic crops can delay the evolution of pest resistance
by providing susceptible insects harbored in the refuges for mating
with resistant insects. The crops in the refuge are likely to sustain
heavy damage and, thus, farmers will incur yield losses. A refuge
kept completely free of pesticides must be 20 to 30 percent the size
of the engineered plot, but the refuge should be about 40 percent
the size of the biotechnology plot if pesticides are to be used, since
insecticide spraying can increase the odds of Bt resistance developing
(Mellon and Rissler 1999).
If,
instead, 30 percent of arable land was devoted to growing soybeans
in a strip cropping design (as many alternative farmers do in the
Midwest), yields of up to 10 percent over comparable monocultures
of corn and soybeans would be achieved, as well as introducing potentials
for internal rotation in the field and contour arrangements of strips
to minimize erosion on hillsides (Ghaffarzadeh et al. 1999). Moreover,
European corn borer would be minimized, as pest populations tend to
be lower in mixed and rotational cropping systems (Andow 1991).
In
the case of cotton, there is no demonstrated need to introduce Bt
toxin in the crop at all, as most Lepidopteran (butterfly and moth)
pests of this crop are pesticide-induced secondary pests. The best
way to deal with them is not to spray insecticides, but instead use
biological control or cultural techniques, such as rotation or strip-cropping
with alfalfa. In the Southwest, the key pest is the boll weevil, a
beetle immune to the Bt toxin.
What
are the costs to US farmers?
To assess
farm economics and the impact of transgenic crops on United States
farms, it is useful to examine the realities faced by Iowa farmers
who live in the heartland of transgenic corn and soy. While weeds
are an annoyance, the real problem they face is falling farm prices,
driven down by long term overproduction. From 1990 to 1998, the average
price of a metric ton of soybeans decreased 62 percent, and returns
over non-land costs declined from $530 to $182 per hectare, a 66 percent
drop. Faced with falling returns per hectare, farmers have no choice
but to ⌠get big or get out.÷ Only by increasing acreage to compensate
for falling per acre profits can farmers stay in business. Any technology
that facilitates ⌠getting big÷ will be seized upon, even if
short term gains are wiped out by prices that continue to fall as
the industrial agricultural model expands.
For
these Iowa farmers, reductions in return per unit of cropland have
reinforced the importance of herbicides within the production process,
as they reduce time devoted to mechanical cultivation and allow a
given farmer to farm more acres. A survey of Iowa farmers conducted
in 1998 indicated that the use of glyphosate with glyphosate resistant
soybean varieties reduced weed control costs by nearly 30 percent
compared with conventional weed management for non-transgenic varieties.
However, yields for the glyphosate resistant soybeans were about four
percent lower, and net returns per unit land area from glyphosate
resistant and conventional soybeans were nearly identical (Duffy 1999).
From
the standpoint of convenience and cost reduction, the use of broad-spectrum
herbicides in combination with herbicide resistant varieties appeals
to farmers. Such systems fit well with large scale operations, no-tillage
production, and sub-contracted chemical applications. However, from
the standpoint of price, any penalty for transgenic varieties in the
marketplace will make the impact of existing low prices even worse.
Taking into account that American exports of soybeans to the European
Union plummeted from 11 million tons to six million in 1999 due to
rejection of GMOs (genetically modified organisms) by European consumers,
it is easy to predict disaster for farmers dependent on transgenic
crops. Durable solutions to the dilemmas facing Iowa farmers will
not come from herbicide-tolerant crops, but from a fundamental restructuring
of Midwest agriculture (Brummer 1998).
The
integration of the seed and chemical industries appears to accelerate
increases in per acre expenditures for seeds plus chemicals delivering
significantly lower returns to growers. Companies developing herbicide
tolerant crops are trying to shift as much per acre cost as possible
from the herbicide onto the seed by seed costs and technology charges.
Increasingly, price reductions for herbicides will be limited to growers
purchasing technology packages. In Illinois, the adoption of herbicide
resistant crops makes for the most expensive soybean seed-plus-weed
management system in modern history∙between $40 and $60 per
acre depending on fee rates, weed pressure, and so on. Three years
ago, the average seed-plus-weed control costs on Illinois farms was
$26 per acre, and represented 23 percent of variable costs. Today,
they represent 35 to 40 percent (Carpenter and Gianessi 1999). Many
farmers are willing to pay for the simplicity and robustness of the
new weed management system, but such advantages may be short lived
as ecological problems arise.
But
as emphasized before, the ultimate cost that farmers pay is their
increased dependence on the biotechnological inputs protected by a
ruthless system of intellectual property rights that legally inhibits
the right of farmers to reproduce, share, and store seed (Busch et
al. 1990). Farmers who exert this right by breaking the signed contract
with a corporation stand to lose their farms.
Will
biotechnology benefit poor farmers?
Most
biotechnological innovations available today bypass poor farmers,
as these farmers are not able to afford the seeds, which are protected
by patents owned by biotech corporations. Extending modern technology
to resource-poor farmers has been historically constrained by considerable
environmental obstacles. An estimated 850 million people live on land
threatened by desertification. Another 500 million reside on terrain
that is too steep to cultivate. Because of those and other limitations,
about two million people have been untouched by modern agricultural
science. Most of the rural poor live in the latitudinal band between
the Tropic of Cancer and the Tropic of Capricorn, a region that is
the most vulnerable to the effects of global warming. In such environments,
a plethora of cheap and locally accessible technologies must be available
to enhance rather than limit farmers options, a trend that corporate
controlled biotechnology inhibits.
Biotech
researchers pledge to counter problems associated with food production
in such marginal areas by developing GM crops with traits considered
desirable by small farmers, such as enhanced competitiveness against
weeds and drought tolerance. However, these new attributes would not
necessarily be a panacea. Traits such as drought tolerance are polygenic∙determined
by the interaction of multiple genes. Consequently, the development
of crops with such traits is a complex process that could take at
least 10 years.
Under
these circumstances, genetic engineering does not give you something
for nothing. When you tinker with multiple genes to create a desired
trait, you inevitable end up with sacrificing other traits, such as
productivity. As a result, use of a drought-tolerant plant would boost
crop yields by only 30 to 40 percent. Any additional yield increases
would have to come from improved environmental practices (such as
water harvesting or enhancing soil organic matter for improved moisture
retention) rather than from the genetic manipulation of specific characteristics
(Persley and Lantin 2000).
Even
if biotechnology could contribute to increased crop harvests, poverty
will not necessarily decline. Many poor farmers in developing countries
do not have access to cash, credit, technical assistance, or markets.
The so-called Green Revolution of the 1950s and 1960s bypassed such
farmers because planting the new high yield crops and maintaining
them through the use of pesticides and fertilizers was too costly
for impoverished landowners. Data shows that, in both Asia and Latin
America, wealthy farmers with larger and better-endowed lands gained
the most from the Green Revolution, where farmers with fewer resources
often gained little (LappΘ et al. 1998). The ⌠Gene Revolution÷
might only end up repeating the mistakes of its predecessor. Genetically
modified seeds are under corporate control and patent protection,
consequently making them very expensive. Since many developing countries
still lack the institutional infrastructure and low interest credit
necessary to deliver these new seeds to poor farmers, biotechnology
will only exacerbate marginalization.
Poor
farmers do not fit into the marketing niche of private corporations,
which focus on biotechnological innovations for the commercial-agricultural
sectors of industrial and developing nations, where these corporations
can expect a huge return on their research investment. The private
sector often ignores important crops such as cassava, which is a staple
for 500 million people worldwide. The few impoverished landowners
who will have access to biotechnology will become dangerously dependent
on the annual purchase of genetically modified seeds. These farmers
will have to abide by onerous intellectual property agreements not
to plant seeds yielded from a harvest of bioengineered plants. Such
stipulations are an affront to traditional farmers, who for centuries
have saved and shared seeds as part of their cultural legacy (Kloppenburg
1998).
Some
scientists and policy makers suggest that large investments through
public-private partnerships can help developing countries acquire
the indigenous scientific and institutional capacity to shape biotechnology
to suit the needs and circumstances of small farmers. But once again,
corporate intellectual property rights to genes and gene-cloning technology
might play spoiler. For instance, Brazil╞s national research
institute (EMBRAPA) must negotiate license agreements with nine different
companies before a virus-resistant papaya developed with researchers
at Cornell University can be released to poor farmers (Persley and
Lantin 2000).
Genetically
Modified Crops and Human Health
Are
transgenic crops similar to conventionally-bred crops?
Government
regulatory agencies consider that crops bred through biotechnology
or conventional plant breeding are ⌠substantially equivalent.÷
This presumption is profoundly flawed and scientifically unsupported.
Most evidence shows that gene transfer using rDNA techniques is substantially
different from the processes that govern gene transfer in traditional
breeding. In such endeavor, plant breeders develop new varieties through
the process of selection and seek to achieve expression of genetic
material which is already present within a species. Conventional crossing
involves the movement of clusters of functionally linked genes, primarily
between similar chromosomes, and including the relevant promoters,
regulatory sequences, and associated genes involved in coordinated
expression of the character of interest in the plant.
Genetic
engineering works primarily through insertion of genetic material
usually from unprecedented sources, that is genetic material from
species, families, and even kingdoms which could not previously be
sources of genetic material for a particular species. The process
involves a ⌠gene gun,÷ a ⌠promoter÷ gene from a virus,
and a marker as a part of the package or construct inserted into the
host plant cell. Current rDNA technologies involve the random insertion
of genes in the absence of normal promoter sequences and associated
regulatory genes. As there are very few examples of plant traits in
which we have identified the associated regulatory genes, the introduction
of a fully µfunctional╞ gene using rDNA techniques is currently
not possible. The rDNA techniques also involve the simultaneous insertion
of viral promoters and selectable markers, and facilitates the introduction
of genes from incompatible species. These genetic transformations
cannot occur using traditional approaches∙which further illustrates
the profound manner in which these two processes differ (Hansen 1999).
In
summary, genetic engineering clearly differs from conventional breeding
as this method relies primarily on selection, using natural process
of sexual and/or asexual reproduction between a species or within
closely related genera. Genetic engineering utilizes a process of
insertion of genetic material, via a gene gun or a special bacterial
truck which does not occur in nature. Biotechnologists can insert
genetic material from any life form into any other, thus creating
novel organisms with which there is no evolutionary experience.
Are
transgenic crop safe to eat?
The premature
commercial release of transgenic crops due to commercial pressures,
and lax FDA and EPA policies which consider genetically modified crops
to be ⌠substantially equivalent÷ to conventional crops, has
occurred in the context of a regulatory framework that seems inadequate,
non-transparent, and, in some cases, completely absent. In fact, approval
for commercial release of transgenic crops is based on scientific
information provided voluntarily by companies producing biotech crops.
It
is estimated that about 50 percent of the corn and soybean based food
in the US comes from genetically modified corn and soybeans. Most
consumers are not aware of this and have no possibility of discerning
transgenic food not labeled as such. Given the fact that no scientist
can ascertain that such foods are completely risk-free, it could be
considered that the majority of the population in the US is being
subjected to a large scale feeding experiment. Consumers in the European
Union (EU) have rejected such GMO foods (LappΘ and Bailey 1998).
Because
of the unusual methods used to breed GM crops, some fear that the
genetic variants produced could introduce foreign substances into
the food supply with unanticipated negative effects on human health.
A major concern is that a protein encoded by an introduced gene may
be allergenic and cause allergic reactions in exposed populations
(Burks and Fuchs 1995).
Biotechnology
is used to introduce genes into various plants that are sources of
food and food components. Introduced traits include insect and virus
resistance, herbicide tolerance, and changes in composition or nutritional
content. Given such diversity of traits, at issue here is the allergenic
potential for proteins introduced into foods from sources with no
history of having allergens or that have amino acid sequence similarities
to known food allergens.
There
is a small but real chance that genetic engineering may transfer new
and unidentified proteins into food, triggering allergic reactions
in millions of consumers who are sensitive to allergens, but have
no way of identifying or protecting themselves from offending foods.
Another
concern is associated with the fact that antibiotic resistance genes
are incorporated into nearly every genetically modified crop plant
as markers to indicate that a plant has been successfully engineered.
It is expected that these genes and their enzyme products, which cause
antibiotics to be deactivated, to be present in engineered foods,
raising important questions about the implications toward human health,
particularly if it compromises human immunity (Ticciati and Ticciati
1998).
Genetic
engineering may remove or deactivate valuable nutritional substance
in food. Recent research shows that GE herbicide resistant soybean
have lower levels (12√14 percent) of isoflavones, key naturally
occurring phytoestrogens (mostly genistin) in soybean, that may protect
women from severe forms of cancer (LappΘ et al. 1998).
There
is no scientist that can negate the possibility that changing the
fundamental genetic make-up of a food could cause new diseases or
health problems. There are no long term studies to prove the safety
of genetically modified crops. These products are not being thoroughly
tested before they arrive on the grocery shelves. Rather, they are
being tested on consumers.
Biotechnology,
Agriculture, and the Environment
Biotechnology
is being pursued to repair the problems (e.g. pesticide resistance,
pollution, soil degradation, etc.) caused by previous agrochemical
technologies promoted by the same companies now leading the bio-revolution.
Transgenic crops developed for pest control closely follow the paradigm
of using a single control mechanism (a pesticide) that has proven
to fail repeatedly with insects, pathogens, and weeds (National Research
Council 1996). The touted ⌠one gene√one pest÷ approach
can be easily overcome by pests that are continuously adapting to
new situations and evolving detoxification mechanisms (Robinson 1996).
Agricultural
systems developed with transgenic crops favor monocultures characterized
by dangerously high levels of genetic homogeneity, leading to higher
vulnerability of agricultural systems to biotic and abiotic stresses
(Robinson 1996). By promoting monocultures it also undermines ecological
methods of farming, such as rotation and multicropping, exacerbating
the problems of conventional agriculture (Altieri 2000).
As
new GE seeds replace the old traditional varieties and their wild
relatives, genetic erosion will accelerate in the Third World (Fowler
and Mooney 1990). The push for uniformity will not only destroy the
diversity of genetic resources, but also disrupt the biological complexity
that underlies the sustainability of indigenous farming systems (Altieri
1996).
There
are many unanswered ecological questions regarding the impact of the
release of transgenic plants and microorganisms into the environment,
and the available evidence supports the proposition that the impact
can be substantial. Among the major environmental risks associated
with genetically engineered plants are the unintended transfer to
plant relatives of ⌠transgenes÷ and the unpredictable ecological
effects (Rissler and Mellon 1996).
Herbicide
resistance
By creating
crops resistant to its herbicides, a biotech company can expand markets
for its patented chemicals. (In 1997, 50,000 farmers grew 3.6 million
hectares of herbicide resistant soybeans, equivalent to 13 percent
of the 71 million national soybean acreage in the US.) Observers gave
a value of $75 million for herbicide resistant crops in 1995, the
first year they were marketed, indicating that by the year 2000 the
market will be approximately 805 million dollars, representing a 61
percent growth (Carpenter and Gianessi 1999).
The
continuous use of herbicides such as bromoxynil and glyphosate (also
known as Roundup by Monsanto), which herbicide resistant crops tolerate,
can lead to problems (Goldberg 1992). It is well documented that when
a single herbicide is used repeatedly on a crop, the chances of herbicide
resistance developing in weed populations greatly increases (Holt
et al. 1993). About 216 cases of pesticide resistance have been reported
in one or more herbicide chemical families (Holt and Le Baron 1990).
Triazine herbicides have the most resistant weed species (about 60).
Given
industry pressures to increase herbicide sales, acreage treated with
broad spectrum herbicides will expand, exacerbating the resistance
problem. For example, it has been projected that the acreage treated
with glyphosate will increase to nearly 150 million acres. Although
glyphosate is considered less prone to weed resistance, the increased
use of the herbicide will result in weed resistance, even if more
slowly. This has already been documented with Australian populations
of annual ryegrass, quackgrass, birdsfoot trefoil, Cirsium arvense
and Eleusine indica (Altieri 2000).
Herbicides
kill more than weeds
Biotech
companies claim that when properly applied, bromoxynil and glyphosate
degrade rapidly in the soil, do not accumulate in ground water, have
no effects on non-target organisms, and leave no residue in foods.
However, there is evidence that bromoxynil causes birth defects in
laboratory animals, is toxic to fish, and may cause cancer in humans
(Goldberg 1992). Because bromoxynil is absorbed through the skin,
and because it causes birth defects in rodents, it is likely to pose
hazards to farmers and farm workers. Similarly, glyphosate has been
reported to be toxic to some non-target species in the soil∙both
to beneficial predators such as spiders, mites, and carabid and coccinellid
beetles, and to detritivores such as earthworms, as well as to aquatic
organisms, including fish (Paoletti and Pimentel 1996). As this herbicide
is known to accumulate in fruits and tubers because it suffers little
metabolic degradation in plants, questions about food safety also
arise, especially now that more than 37 million pounds of this herbicide
are used annually in the US alone. Moreover, research has shown that
glyphosate seems to act in a similar fashion to antibiotics by altering
in a yet unknown way soil biology and causing effects such as:
- Reducing
the ability of soybeans and clover to fix nitrogen
- Rendering
bean plants more vulnerable to disease.
- Reducing
growth of beneficial soil-dwelling mycorrhizal fungi, which are
key for helping plants extract phosphorous from the soil.
Creation
of "superweeds"
Although
there is some concern that transgenic crops themselves might become
weeds, the major ecological risk is that large scale releases of transgenic
crops may promote transfer of transgenes from crops to other plants,
which then could become weeds (Darmency 1994). Transgenes that confer
significant biological advantage may transform wild/weedy plants into
new or worse weeds (Rissler and Mellon 1996). The biological process
of concern here is introgression∙hybridization among distinct
plant species. Evidence indicates that such genetic exchanges among
wild, weed, and crop plants already occur. The incidence of shattercane
(Sorghum bicolor), a weedy relative of sorghum and the gene
flows between maize and teosinte demonstrate the potential for crop
relatives to become serious weeds. This is worrisome given that a
number of US crops are grown in close proximity to sexually compatible
wild relatives (Lutman 1999). Extreme care should be taken in plant
systems exhibiting easy cross pollination, such as oats, barley, sunflowers,
and wild relatives and between rapeseed and related crucifers (Snow
and Moran 1997).
In
Europe, there is a major concern about the possibility of pollen transfer
of herbicide tolerant genes from Brassica oilseeds to Brassica
nigra and Sinapis arvensis (Casper and Landsmann 1992).
There are also crops that are grown near wild weedy plants that are
not close relatives but may have some degree of cross compatibility
such as the crosses of Raphanus raphanistrum X R. Sativus
(radish) and Johnson grass X Sorghum corn (Radosevich, et al.
1996). Cascading repercussions of these transfers may ultimately mean
changes in the make-up of plant communities. Gene exchanges pose major
threats to centers of diversity, where in biodiverse farming systems
the probability for transgenic crops of finding sexually compatible
wild relatives is very high.
Transfer
of genes from transgenic crops to organically grown crops poses a
specific problem to organic farmers; organic certification depends
on the growers being able to guarantee that their crops have no inserted
genes. Crops able to outbreed, such as maize or oilseed rape, will
be affected to the greatest extent, but all organic farmers are at
risk of genetic contamination. There are no regulations that enforce
minimum isolating distances between transgenic and organic fields
(Royal Society 1998).
In
conclusion, the fact that interspecific hybridization and introgression
are common to species such as sunflower, maize, sorghum, oilseed rape,
rice, wheat, and potatoes provides a basis to expect gene flow between
transgenic crops and wild relatives to create new herbicide resistant
weeds (Lutman 1999). There is consensus among scientists that transgenic
crops will eventually allow transgenes to escape into free living
populations of wild relatives. The disagreements lay in how serious
the impact will be from such transfers (Snow and Moran 1997).
Environmental
Risks of Insect Resistant Crops (Bt Crops)
Resistance
According
to the biotech industry, the promise of transgenic crops inserted
with Bt genes is the replacement of synthetic insecticides now used
to control insect pests. But this is not so clear because most crops
have a diversity of insect pests and insecticides will still have
to be applied to control non-Lepidoptera pests, which are not susceptible
to the Bt toxin expressed by the crop (Gould 1994). In fact, in a
recent report (USDA 1999) an analysis of pesticide use in the 1997
US growing season in 12 region/crop combinations showed that in seven
sites there was no statistically significant difference in pesticide
use on Bt crops versus non-Bt crops. In the Mississippi Delta, significantly
more pesticides were used on Bt versus non-Bt cotton.
On
the other hand, several Lepidoptera species have been reported to
develop resistance to Bt toxin in both field and laboratory tests,
suggesting that major resistance problems are likely to develop in
Bt crops, which through the continuous expression of the toxin create
a strong selection pressure (Tabashnik 1994). No serious entomologist
questions whether resistance will develop or not. The question is
how fast? Scientists have already detected development of ⌠behavioral
resistance÷ by some insects that take advantage of the uneven expression
of toxin potency within crop foliage, thus attacking tissue patches
with low toxin concentrations. Moreover, as genetically inserted toxins
often decrease in leaf and stem litter as crops reach maturation,
the low dose can only kill or debilitate completely susceptible larvae
(homozygotes); consequently, adaptation to the Bt toxin can occur
much faster if the concentration always remained high. Observation
of transgenic corn plants in late October indicated that most European
corn borers that survived had entered dormancy in preparation for
emergence in the following spring as adults (Onstad and Gould 1998).
In
order to delay the inevitable development of resistance by insects
to Bt crops, bioengineers are preparing resistance management plans,
which consist of patchworks of transgenic and non-transgenic (called
refuges) to delay the evolution of resistance by providing susceptible
insects for mating with resistant insects. Although refuges should
be in size at least 30 percent of the crop area, according to members
of the Campaign for Food Safety, Monsanto╞s new plan calls for
only 20 percent refuges even when insecticides are to be used. Moreover,
the plan offers no details whether the refuges must be planted alongside
the transgenic crops, or at some distance away, where studies suggest
they would be less effective (Mallet and Porter 1992). In addition
to refuges requiring the difficult goal of regional coordination between
farmers, it is unrealistic to expect most small and medium sized farmers
to devote up to 30√40 percent of their crop area to refuges,
especially if crops in these areas are to sustain heavy pest damage.
The
farmers that face the greatest risk from the development of insect
resistance to Bt are neighboring organic farmers who grow corn and
soybeans without agrochemicals. Once resistance appears in insect
populations, organic farmers will not be able to use Bacillus thuringiensis
in its microbial insecticide form to control the Lepidoptera pests
that move in from adjacent neighboring transgenic fields. In addition,
genetic pollution of organic crops resulting from gene flow (pollen)
from transgenic crops can jeopardize the certification of organic
crops and organic farmers may lose premium markets. Who will compensate
the farmers for such losses?
We
know from the history of agriculture that plant diseases, insect pests,
and weeds become more severe with the development of monocultures,
and that intensively managed and genetically manipulated crops soon
lose genetic diversity (Altieri 1994; Robinson 1996). Given these
facts, there is no reason to believe that resistance to transgenic
crops will not evolve among insects, weeds, and pathogens as has happened
with pesticides. No matter what resistance management strategies will
be used, pests will adapt and overcome the agronomic constraints (Green
1990). Studies of pesticide resistance demonstrate that unintended
selection can result in pest problems that are greater than those
that existed before deployment of new insecticides. Diseases and pests
have always been amplified by changes toward genetically homogenous
agriculture, precisely the type of farming that biotechnology promotes
(Robinson 1996).
Effects
on non-target species
By keeping
pest populations at extremely low levels, Bt crops could potentially
starve natural enemies, as predators and parasitic wasps that feed
on pests need a small amount of prey to survive in the agroecosystem.
Among the natural enemies that live exclusively on insects which the
transgenic crops are designed to kill (Lepidoptera), egg and larval
parasitoids would be most affected because they are totally dependant
on live hosts for development and survival, where some predators could
theoretically thrive on dead or dying prey (Schuler et al. 1999).
Natural
enemies could also be affected directly through inter-trophic level
effects of the toxin. The potential of Bt toxins moving through insect
food chains poses serious implications for natural biocontrol in agricultural
fields. Recent evidence shows that the Bt toxin can affect beneficial
insect predators that feed on insect pests present on Bt crops (Hilbeck
1998). Studies in Switzerland show that mean total mortality of predaceous
lacewing larvae (Chrysopidae) raised on Bt fed prey was 62
percent compared to 37 percent when raised on Bt-free prey. These
Bt prey fed Chrysopidae also exhibited prolonged development time
throughout their immature life stage (Hilbeck 1998).
These
findings are of concern to small farmers who rely on the rich complex
of predators and parasites associated with their mixed cropping systems
for insect pest control (Altieri 1994). Inter-trophic level effects
of the Bt toxin raise serious concerns about the potential of the
disruption of natural pest control. Polyphagous predators that move
within and between mixed crops cultivars will encounter Bt-containing
non-target prey throughout the crop season (Hilbeck 1999). Disrupted
biocontrol mechanisms may result in increased crop losses due to pests
or to increased use of pesticide by farmers, with consequent health
and environmental hazards.
It
is also now known that windblown pollen from Bt crops found on natural
vegetation surrounding transgenic fields can kill non-target insects.
A Cornell University study (Losey et al. 1999) showed that corn pollen
containing Bt toxin can drift several meters downwind and deposit
itself on milkweed foliage with potentially damaging effects on monarch
butterfly populations. These findings open a whole new dimension on
the unexpected impacts of transgenic crops on non-target organisms
which play key and many times unknown roles in the ecosystem.
But
the environmental effects are not limited to crops and insects. Bt
toxins can be incorporated into the soil though leaf materials, when
farmers plow under transgenic crop residues after harvest. Toxins
may persist for two to three months, resisting degradation by binding
to clay and humic acid soil particles while maintaining toxin activity
(Palm et al. 1996). Such active Bt toxins that end up and accumulate
in the soil and water from transgenic leaf litter may have negative
impacts on soil and aquatic invertebrates and nutrient cycling processes
(Donnegan and Seidler 1999).
The
fact that Bt retains its insecticidal properties and is protected
against microbial degradation by being bound to soil particles, persisting
in various soils for at least 234 days, is of serious concern for
poor farmers who cannot purchase expensive chemical fertilizers. These
farmers instead rely on local residues, organic matter, and soil microorganisms
for soil fertility (key invertebrate, fungal, or bacterial species),
which can be negatively affected by the soil-bound toxin (Saxena et
al. 1999).
A
precautionary tale
The ecological
effects of genetically engineered crops are not limited to pest resistance
and creation of new weeds or virus strains. As argued herein, transgenic
crops can produce environmental toxins that move through the food
chain and also may end up in the soil and water affecting invertebrates
and probably ecological processes such as nutrient cycling. Moreover,
the large scale landscape homogenization with transgenic crops will
exacerbate the ecological vulnerability already associated with monoculture
agriculture (Altieri 2000). Unquestioned expansion of this technology
into developing countries is not desirable. There is strength in the
agricultural diversity of many of these countries, and it should not
be inhibited or reduced by extensive monoculture, especially when
consequences of doing so results in serious social and environmental
problems (Thrupp 1998).
Despite
these concerns, transgenic crops have been rushed into international
markets and massively deployed in the agricultural landscapes of the
US, Canada, Argentina, China, and other countries. It is unfortunate
that only now, after four years of massive commercial use of transgenic
crops, former US Secretary of Agriculture, Dan Glickman, has called
for studies to assess the long term ecological and health effects
of these crops. This comes a bit late, given that the ecological release
of genes is non-retrievable and their effects irreversible.
The
rapid release of transgenic crops and the ensuing financial disarray
(share prices for biotechnology companies are sinking toward all-time
lows) is disturbingly reminiscent of the earlier uncritical bandwagons
for nuclear energy and chlorinated pesticides like DDT. A combination
of public opposition and financial liability eventually forced retrenchment
of these earlier technologies, after their effects on the environment
and human health proved to be far more complex, diffuse, and lingering
than the promises that accompanied their rapid commercialization.
In
the context of negotiations within the Convention on Biological Diversity
(CBD) last year, 130 countries have shown wisdom in adopting the ⌠precautionary
principle÷ by signing a global treaty that governs the trade of genetically
modified organisms (GMOs). The precautionary principle holds that
when a new technology may cause suspected harm, scientific uncertainty
as to the scope and severity of the harm should not prevent precautionary
action. Instead of requiring critics to prove that the technology
poses potential damages, the producers of the technology shoulder
the burden of presenting evidence that the technology is safe. There
is a clear need for independent testing and monitoring to make sure
that self-generated data presented to government regulatory agencies
is not biased or twisted to accommodate industry interests. Moreover,
a worldwide moratorium should be enforced on GMOs until the questions
raised both by credible scientists who are seriously investigating
the ecological and health impacts of transgenic crops, and by the
public at large, can be cleared up by independent bodies of scientists.
Many
environmental and consumer groups advocating for a more sustainable
agriculture demand continued support for ecologically based agricultural
research∙all the biological problems that biotechnology aims
at can be solved using agrochemical approaches. The problem is that
research at public institutions increasing reflects the interests
of private funding groups at the expense of public good research such
as biological control, organic production systems, and general agroecological
techniques (Busch 1990). Civil society must request for more research
on alternatives to biotechnology by universities and other public
organizations. There is also an urgent need to challenge the patent
system and intellectual property rights intrinsic to the World Trade
Organization (WTO), which not only provide multinational corporations
with the right to seize and patent genetic resources, but that also
accentuate the rate at which market forces already encourage monoculture
cropping with genetically uniform transgenic varieties.
More
Sustainable Alternatives to Biotechnology Do Exist
What
is agroecology?
Proponents
of the second Green Revolution argue that developing countries should
opt for an agro-industrial model that relies on standardized technologies
and ever-increasing fertilizer and pesticide use to provide additional
food supplies for growing populations and economies. In contrast,
a growing number of farmers, NGOs, and sustainable agriculture advocates
propose that instead of this capital and input intensive approach,
developing countries should favor an agroecological model, which emphasizes
biodiversity, recycling of nutrients, synergy among crops, animal,
soils, and other biological components, as well as regeneration and
conservation of resources (Altieri 1996).
A
sustainable agricultural development strategy that is environmentally
enhancing must be based on agroecological principles and on a more
participatory approach for technology development and dissemination.
Agroecology is the science that provides ecological principles for
the design and management of sustainable and resource-conserving agricultural
systems∙offering several advantages for the development of farmer-friendly
technologies. Agroecology relies on indigenous farming knowledge and
selected low input modern technologies to diversify production. The
approach incorporates biological principles and local resources into
the management of farming systems, providing an environmentally sound
and affordable way for small farmers to intensify production in marginal
areas (Altieri et al. 1998).
It
is estimated that approximately 1.9 to 2.2 billion people remain directly
or indirectly untouched by modern agricultural technology. In Latin
America, the rural population is projected to remain stable at 125
million until the year 2000, but over 61 percent of this population
is poor and expected to increase. The projections for Africa are even
more dramatic. The majority of the rural poor (about 370 million of
the poorest) live in areas that are resource-poor, highly heterogeneous,
and risk prone. Their agricultural systems are small scale, complex,
and diverse. The worst poverty is often located in arid or semi-arid
zones, and in mountains and hillsides that are ecologically vulnerable.
Such farms and their complex farming systems pose tough challenges
to researchers.
To
be of benefit to the rural poor, agricultural research and development
should operate on the basis of a ⌠bottom-up÷ approach, using
and building on the resources already available∙local people,
their knowledge, and their indigenous natural resources. It must also
seriously take into consideration, through participatory approaches,
the needs, aspirations, and circumstances of small farmers. This mean
that from the standpoint of poor farmers, innovations must:
- Save
inputs and reduce costs.
- Reduce
risk.
- Expand
toward marginal-fragile lands.
- Be
congruent with peasant farming systems.
- Improve
nutrition, health, and environment.
It
is precisely because of the above requirements that agroecology offers
several advantages over Green Revolution and biotech approaches. Agroecological
technologies are:
- Based
on indigenous knowledge and rationale.
- Economically
viable, accessible, and based on local resources.
- Environmentally
sound, socially and culturally sensitive.
- Risk
averse, adapted to farmer circumstances.
- Enhancing
of total farm productivity and stability.
Thousand
of examples exist of rural producers, in partnerships with NGOs and
other organizations, promoting resource-conserving yet highly productive
farming systems, while meeting the above criteria. Increases in production
of 50 to 100 percent are fairly common with most alternative production
methods. In some of these systems, yields for crops that the poor
rely on most∙rice, beans, maize, cassava, potatoes, barley∙have
been increased by several-fold, relying on labor and local know-how
more than on expensive purchased inputs, and capitalizing on processes
of intensification and synergy. More important than just yields, it
is possible to raise total production significantly through diversification
of farming systems, using available resources as much as possible
(Uphoff and Altieri 1999).
There
are many examples of the application of agroecology throughout the
developing world. It is estimated that about 1.45 million poor rural
households covering about 3.25 million hectares have adopted resource
conserving technologies. Some examples include (Pretty 1995):
- Brazil:
200,000 farmers using green manures/cover crops doubled maize
and wheat yields.
- Guatemala-Honduras:
45,0000 farmers using the legume Mucuna as a cover for soil conservation
systems tripled maize yields in hillsides.
- Mexico:
100,000 small organic coffee producers increased production by
half.
- Southeast
Asia: 100,000 small rice farmers involved in IPM farmers schools
substantially increased yields while eliminating pesticides.
- Kenya:
200,000 farmers using legume-based agroforestry and organic inputs
doubled maize yields.
Some
success stories from Latin America:
Stabilizing
the Hillsides of Central America: Perhaps the major agricultural challenge
in Latin America has been to design cropping systems for hillside
areas that are productive and reduce erosion. World Neighbors took
on this challenge in Honduras in the mid-1980s. The program introduced
soil conservation practices such as drainage and contour ditches,
grass barriers, and rock walls, and organic fertilization methods,
such as the use of chicken manure and intercropping with legumes.
Grain yields tripled, and in some cases quadrupled, from 400 kilograms
per hectare to 1200√1600 kilograms. The yield increase has ensured
that the 1200 families participating in the program have ample grain
supplies.
Several
NGOs in Central America have promoted the use of legumes as green
manure, an inexpensive source of organic fertilizer. Farmers in northern
Honduras are using velvet beans with excellent results. Corn yields
are more than double the national average, erosion and weeds are under
control, and land preparation costs are lower. Taking advantage of
well-established farmer-to-farmer networks in Nicaragua, more than
1000 peasants recovered degraded land in the San Juan watershed in
just one year after using this simple technology. These farmers have
decreased use of chemical fertilizers from 1900 to 400 kilograms per
hectare, while increasing yields from 700 to 2000 kilograms per hectare.
Their production costs are about 22 percent lower than those for farmers
using chemical fertilizers and monocultures.
Moreover.
hillside farmers adapting these soil conservation systems suffered
significantly lower damage (mud slides and soil loss) than monoculture
farms during hurricane Mitch in 1998.
Recreating
Incan Agriculture: In 1984, several NGOs and state agencies assisted
local farmers in Puno-Peru to reconstruct ancient systems (waru-warus)
consisting of raised fields surrounded by ditches filled with water.
These fields produced bumper crops despite killing frosts common at
altitudes of 4000 meters. The combination of raised beds and canals
moderates soil temperature, thereby extending the growing season and
leading to higher productivity on the waru-warus than on chemically
fertilized normal pampa soils. In the district of Huatta, the waru-warus
have produced annual potato yields of eight to 14 metric tons per
hectare, contrasting favorable with the average regional potato yields
of one to four metric tons per hectare.
Various
NGOs and governmental agencies in the Colca Valley of southern Peru
have sponsored terrace reconstruction by offering peasants low interest
loans or seeds and other inputs to restore abandoned terraces. First
year yields of potatoes, maize, and barley showed a 43 to 65 percent
increase compared to yields from sloping fields. A native legume was
used as a rotational or associated crop on the terraces to fix nitrogen,
minimizing fertilizer needs and increasing production. Studies in
Bolivia, where native legumes have been used as rotational crops,
show that though yields are greater in chemically fertilized and mechanically
operated potato fields, energy costs are higher and net economic benefits
lower than with the agroecological system.
Integrated
Farms: A number of NGOs have promoted diversified farms in which each
component of the farming system biologically reinforces the other
components∙wastes from one component, for instance, become inputs
to another. Since 1980, the NGO CET has helped peasants in south-central
Chile reach year-round food self-sufficiency while rebuilding the
productive capacity of the land. Small model farm systems, consisting
of polycultures and rotating sequences of forage and food crops, forest
and fruit trees, and animals, have been set up. Components are chosen
according to their nutritional contributions to subsequent rotations,
their adaptability to local agro-climatic conditions, local peasant
consumption patterns, and market opportunities.
Soil
fertility of these farms has improved and no serious pest or disease
problems have appeared. Fruit trees and forage crops achieve higher
than average yields, and milk and egg production far exceeds that
of conventional high input farms. A nutritional analysis of the system
shows that for a typical family, it produces 250 percent surplus of
protein, 80 and 550 percent surpluses of Vitamin A and C, respectively,
and 330 percent surplus of calcium. If all of the farm output were
sold at wholesale prices, the family could generate a monthly net
income one and a half times greater than the monthly legal minimum
wage in Chile, while dedicating only a few hours per week to the farm.
The time freed up is used by farmers for other on and off farm income-generating
activities.
Recently,
a Cuban NGO helped establish a number of integrated farming systems
in cooperatives in the province of Havana. Several polycultures, such
as cassava√beans√maize, cassava√tomato√maize,
and sweet potato√maize were tested in the cooperatives. The
productivity of these polycultures was 1.45 to 2.82 times greater
than the productivity of the monocultures. The use of green manure
ensured a production of squash equivalent to that obtainable by applying
175 kilograms of urea per hectare. In addition, such legumes improved
the physical and chemical characteristics of the soil and effectively
broke the cycle of insect pest infestations.
The
examples summarized above (see also Altieri 2000) are a small sample
of the thousands of successful experiences of sustainable agriculture
implemented at the local level. Data show that over time agroecological
systems exhibit more stable levels of total production per unit area
than high input systems; produce economically favorable rates of return;
provide a return to labor and other inputs sufficient for a livelihood
acceptable to small farmers and their families; and ensure soil protection
and conservation and enhance agro-biodiversity. More importantly,
these experiences, which emphasize farmer-to-farmer research and grassroots
extension approaches, represent countless demonstrations of talent,
creativity, and scientific capability in rural communities. They point
to the fact that human resource development is the cornerstone of
any strategy aimed at increasing options for rural people and especially
resource-poor farmers.
Organic
farming
Agroecological
approaches can also benefit medium to large farmers involved in commercial
agriculture both in the developing world, as well as the US and Europe
(Lampkin 1990). Much of the area under organic farming is based on
agroecology and it is widespread throughout the world, reaching about
seven million hectares of which half are in Europe and about 1.1 million
in the United States. In Germany alone there are about eight thousand
organic farms occupying about two percent of the total arable land.
In Italy, organic farms number around 18,000 and in Austria about
20,000 organic farms account for 10 percent of total agricultural
output.
In
1980 the US Department of Agriculture (USDA) estimated that there
were at least eleven thousand organic farms in the United States and
at least 24 thousand farms that use some organic techniques. In California,
organic foods are one of the fastest growing segments of the agricultural
economy, with retail sales growing at 20 to 25 percent per year. Cuba
is the only country undergoing a massive conversion to organic farming,
promoted by the drop of fertilizer, pesticides, and petroleum imports
after the collapse of trade relations with the Soviet bloc in 1990.
By promoting agroecological techniques massively in both urban and
rural areas, productivity levels in the island have recovered.
Research
has shown that organic farms can be as productive as conventional
ones, but without using agrochemicals, consuming less energy, and
saving soil and water. In fact, there is a strong body of evidence
that organic methods can produce enough food for all∙and do
it from one generation to the next without depleting natural resources
or harming the environment. In 1989 the National Research Council
wrote up case studies of eight organic farms that ranged from a 400
acres grain/livestock farm in Ohio to 1400 acres of grapes in California
and Arizona. The organic farms╞ average yields were generally
equal to or better than the average yields of the conventional high
intensity farms surrounding them∙once again, they could be sustained
year after year without costly synthetic inputs (NRC 1984).
Recent
studies include long term studies such as the one conducted at the
Farming Systems Trial at the Rodale Institute, a nonprofit research
facility near Kutztown, Pennsylvania. Three kinds of experimental
plots have been tested side by side for nearly two decades. One is
a standard high intensity rotation of corn and soybeans in which commercial
fertilizers and pesticides have been used. Another is an organic system
in which a rotation of grass/legume forage has been added and fed
to cows, whose manure has been returned to the land. The third is
an organic rotation in which soil fertility has been maintained solely
with legume cover crops that have been plowed under. All three kinds
of plots have been equally profitable in market terms. Corn yields
have differed by less than one percent. The rotation with manure has
far surpassed the other two in building soil organic matter and nitrogen,
and it has leached fewer nutrients into ground water. During the record
drought of 1999, the chemically dependent plots yielded just 16 bushels
of soybeans per acre; the legume-fed organic fields delivered 30 bushels
per acre, and the manure-fed organic fields delivered 24 bushels per
acre.
In
what must be the longest-running organic trial in the world∙150
years∙England╞s Rothamsted Experimental Station (also
known as the Institute of Arable Crops Research) reports that its
organic manured plots have delivered wheat yields of 1.58 tons per
acre, compared to synthetically fertilized plots that have yielded
1.55 tons per acre. That may not seem like much but the manured plots
contain six times the organic matter found in the chemically treated
plots.
The
evidence shows that in many ways, organic farming conserves natural
resources and protects the environment more than conventional farming.
Research also shows that soil erosion rates are lower in organic farms,
and that levels of biodiversity are higher in organic farming systems
than in conventional ones. The rationale of both systems are significantly
different: organic systems are based on the assumption that at any
given time, some of the acreage is planted with legume green manure
or fodder crop that will go to feed cows, whose manure will be returned
to the soil. The chemical farms are based on a profoundly different
assumption: that their survival depends on a fertilizer factory somewhere
that is consuming vast amounts of fossil fuels and emitting greenhouse
gases.
What
is needed?
There
is no question that small farmers located in marginal environments
in the developing world can produce much of their needed food. The
evidence is conclusive: new approaches and technologies spearheaded
by farmers, local governments, and NGOs around the world are already
making a sufficient contribution to food security at the household,
national, and regional levels. A variety of agroecological and participatory
approaches in many countries show very positive outcomes even under
adverse conditions. Potentials include: raising cereal yields from
50 to 200 percent, increasing stability of production through diversification
and soil/water management, improving diets and income with appropriate
support and spread of these approaches, and contributing to national
food security and to exports (Uphoff and Altieri 1999).
Whether
the potential and spread of these thousands of local agroecological
innovations is realized depends on investments, policies, and attitude
changes on the part of researchers and policy makers. Major changes
must be made in policies, institutions, and research and development
to make sure that agroecological alternatives are adopted, made equitably
and broadly accessible, and multiplied so that their full benefit
for sustainable food security can be realized. Existing subsidies
and policy incentives for conventional chemical approaches must be
dismantled. Corporate control over the food system must also be challenged.
Governments and international public organizations must encourage
and support effective partnerships between NGOs, local universities,
and farmer organizations in order to assist and empower poor farmers
to achieve food security, income generation, and natural resource
conservation.
Equitable
market opportunities must also be developed, emphasizing fair trade
and other mechanisms that link farmers and consumers more directly.
The ultimate challenge is to increase investment and research in agroecology
and scale up projects that have already proven successful to thousands
of other farmers. This will generate a meaningful impact on the income,
food security, and environmental well being of the world╞s population,
especially of the millions of poor farmers yet untouched by modern
agricultural technology.
Glossary
A
Adaptation:
the process by which an organism undergoes modification so that its
functions are more suited to its environment and its changes.
Adaptive
mutation or directed mutation: the phenomenon whereby bacteria and
yeast cells in stationary (non-growing) phase have some way of producing
(or selectively retaining) only the most appropriate mutations that
enable them to make use of new substrates for growth.
Agbiotech:
short for agricultural biotechnology; the organized application of
genetic manipulations to plants.
Agrobacterium
tumefaciens: a bacterium which causes crown gall disease in a range
of dicotyledonous plants, especially coastal member of the genus Pinus.
The bacterium can enter dead or broken plant cells in a living organism
and transfer a tumor-inducing portion of DNA in the form of a plasmid.
The plasmid then integrates into the plant╞s own genetic material,
constituting a natural form of genetic engineering. Strains of A.
tumefaciens can be artificially engineered to introduce selected foreign
genes of choice into plant cells. By growing the infected cells in
tissue culture, whole plants can be regenerated in which every cell
carries the foreign gene.
Allele:
from ⌠allelomorph÷ meaning one of a series of possible, alternative
forms of a given gene that differ in DNA sequence but produce a similar
product, for instance a blood group or plant protein.
Allergen:
a substance that causes the body to react hypersensitively to it.
Amino
acid: an organic acid carrying an amino acid group (-NH2). There are
twenty different amino acids, which are joined together in a defined
order to make up linear molecules of proteins, each of which contains
hundreds of amino acids.
Antibiotic:
substance which acts to destroy or inhibit the growth of a microbe
(e.g., bacteria or fungi)
Antibody:
common name for an immunoglobulin protein molecule which reacts with
a specific antigen.
Antigen:
a foreign substance capable of eliciting an immunological response
in a vertebrate animal usually of a humoral variety and including
production of an antibody specific to the antigen╞s structural
makeup.
Artificial
selection: the choosing by humans of a genotype that then contributes
to the genetic types that make up the succeeding generations for a
given organism or plant.
B
Bacillus:
a genus of rod-shaped bacteria. Bacillus thuringiensis is a spore
forming soil bacillus that grows in the soils of many regions and
is the source of the toxoid used in genetic engineering (see Bt toxoid).
Bacterium:
a single celled, microscopic organism in the Prokaryote kingdom.
Baculovirus:
a virus that normally infects insects.
Bioengineering:
the construction of a genetically controlled plant or animal by transferring
genes from an otherwise genetically incompatible organism to create
a novel function or product.
Biological
species: groups of individuals which freely share a common set of
genes and are reproductively isolated from each other so that interbreeding
usually cannot occur.
Biotechnology:
the combination of biochemistry, genetics, microbiology, and engineering
to develop products and organisms of commercial value.
Bottleneck
effect: a fluctuation in gene frequencies brought about by the abrupt
contraction of a large population into a smaller one which then expands
again with an altered gene pool.
Brassica:
a genus of plants that includes broccoli and cabbage.
Breeding:
the controlled propagation of plants or animals.
Bromoxynil:
a bromine-containing herbicide produced by Rh≈ne-Poulenc Company
under the name Buctril½.
Bt toxoid:
the crystalline proteins derived from some strains of Bacillus thuringiensis
that is activated to become poisonous in the alkaline environment
of an insect larvae╞s intestinal tract.
C
Carcinogen:
an agent, usually a chemical, that causes cancer.
Cell:
the smallest unit of all living things, capable of self-replication.
Chromosome:
a threadlike structure made up of DNA strands and proteins (histones
and non-histones) that carries genetic information in a linear sequence.
Clone:
an identical copy of an individual or gene, or the totality of all
the identical copies made from an individual or a gene. In genetics,
the clone is identical in genetic make-up to the original.
Crop
lineage: the descendants of a single progenitor of a given food crop.
Crossbreeding:
see outbreeding.
Crossing:
the act of fertilizing one plant with the pollen of the other. Such
cross-pollination can be accomplished, for example, by humans, insects,
or the wind, and can be intentional or not. When crossed by humans,
however, some measure of intention is often assumed.
Cultivar:
a variety of plant produced through selective breeding by humans and
maintained by cultivation.
D
Darwinian
evolution: the preferential reproduction of genetically varied organisms
with specific adaptations that permit their differential survival.
Deoxyribonucleic
acid (see DNA): the molecular basis for heredity.
Diploid:
having a double genetic complement; the genetic material contributed
from two haploid gametes.
DNA:
the genetic material of cells comprised of based, arrayed in an ascending/
descending double helix.
DNA sequence:
the linear array of bases (ATCG), which spells out the genetic code.
Dominant:
form of expression in a gene, in which the phenotype of the dominant
form is expressed over the recessive form.
Dominant
allele: an allele that is expressed when only one copy is present
in an individual, that is, in heterozygous condition.
Dominant
gene: a gene whose products are expressed when only one form of the
gene is present as a single allele (See recessive gene).
E
Ecosystem:
the composite of all the organisms of a given place interacting with
the environment.
Epigenetic:
developmental; any process not involving change in DNA base sequence
in the genome.
Epistasis:
interaction between genes.
Essential
amino acid: one of eight amino acids not synthesized in the human
body, including phelylalanine; methionine; lysine; tryptophan; valine;
leucine; isoleucine and threonine.
Estrogenic:
having the properties of an estrogen, e.g., in stimulating cell growth
or proliferation in specific sexual target tissues.
Eukaryotes:
the superkingdom made up of organisms whose cells contain a true membrane-lined
nucleus.
F
Flavonoids:
molecules found in some plants that may have unpredicted biological
properties, often antioxidant or hormonal in nature.
Flavone:
aromatic molecule (i.e., contains a benzene ring as a core molecule)
significant in the communication of legume plant to Rhizobium and
Bradyrhizobium.
G
Gene:
the unit of heredity consisting of a sequence of DNA bases with ⌠start÷
and ⌠stop÷ information along with the base sequences for a specified
protein.
Gene
amplification: the process whereby genes or sequences of DNA in the
genome are greatly increased in number of copies.
Gene
bank: for plants, normally a temperature and humidity controlled facility
used to store seed (or other reproductive materials) for future use
in research and breeding programs. Also called seed banks.
Gene
cloning: the technique of making many copies of a gene, isolating
the gene, and identifying it.
Gene
expression: in molecular genetics, this usually means the eventual
appearance of the polypeptide encoded by the gene.
Gene
silencing: the process (or processes) whereby certain genes in the
genome are prevented from being expressed by chemical modifications
and other means.
Gene
splicing: the creation of genetic combinations by intentionally interspersing
a novel gene sequence into an existing genome, usually in bacteria.
Genetic
code: the code establishing the correspondence between the sequence
of bases in nucleic acids (DNA and the complementary RNA) and the
sequence of amino acids and proteins.
Genetic
diversity: in a group such as a population or species, the possession
of a variety of genetic traits and alleles that frequently result
in differing expression in different individuals.
Genetic
engineering: those experimental or industrial technologies used to
alter the genome of a living cell so that it can produce more or different
molecules than it is already programmed to make; also, the manipulation
of genes to bypass normal or asexual reproduction.
Genetic
fingerprinting: a method probably initially developed by Alec Jeffreys
which enables genetic relationships between close relative to be established
using DNA technologies.
Genetic
information: the data contained in a sequence of bases in a molecule
of DNA.
Genetic
marker: any segment of DNA that can be identified, or whose chromosomal
location is known, so that it can be used as a reference point to
map or locate other genes; any gene that has an identifiable phenotype
that can be used to track the presence or absence of other genes on
the same piece of DNA transferred into a cell.
Genetic
resources: the term is essentially synonymous with germplasm as used
in this book, except that it carries with it a stronger implication
that the material has or is seen as having economic or utilitarian
value.
Genome:
all of the genes carried by a given organism.
Germplasm:
the material in the germ cells that supposedly accounts for the unchanging
hereditary influence that is passed on to subsequent generations.
Glyphosate:
the active ingredient in the herbicide Round-UpTM.
GMO:
abbreviation for Genetically Modified Organism; a plant or animal
containing permanently altered genetic material.
H
Haploid:
containing only half the normal complement of chromosomes; the genetic
complement of the gametes.
Herbicide:
a pesticide that usually affects only plants; a chemical with killing
or growth inhibiting effects on plants.
Heterozygote:
an individual who has two different alleles of a gene.
Heterozygous:
a condition in which two different alleles of the gene are present
in an individual.
Homogeneity:
having the same form or content.
Homologous:
similar; derived from a common ancestor.
Homozygosity:
having the same allele on both parental chromosomal strands; the state
of being homozygous.
Homozygote:
an individual who has two identical alleles of the gene.
Horizontal
gene transfer: the transfer of genes from one individual to another,
of the same or different species, usually by means other than cross-breeding.
Hybrid:
an organism derived from two distinct, and usually homozygous, parental
lines.
I
Inbred
line: a line produced by inbreeding. In plant breeding a nearly homozygous
line usually originating by continued self-fertilization, accompanied
by selection. See also pure line.
Inbreeding:
the mating of individuals more closely related that individuals mating
at random.
Introgression:
the introduction of genes from one member of the species into another
where the donor is often geographically or morphologically distant
from the recipient. See introgressive hybridization.
Introgressive
hybridization: the incorporation of genes of one species into the
gene pool of another usually resulting in a population of individuals
which continue