ISIS Report 13/06/12Syngenta Charged for Covering up Livestock Deaths from GM Corn
Corporation faces criminal charges for concealing own study in which cows died after eating its genetically modified corn Dr Eva Sirinathsinghji http://www.i-sis.org.uk/
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Biotech
giant Syngenta has been criminally charged with denying knowledge that
its genetically modified (GM) Bt corn kills livestock during a civil
court case that ended in 2007 [1].
Syngenta’s Bt 176 corn variety expresses an insecticidal Bt toxin (Cry1Ab) derived from the bacterium, Bacillus thuringiensis (Bt)
and a gene conferring resistance to
glufosinate herbicides. EU cultivation of Bt 176 was discontinued in
2007. Similar varieties however, including Bt 11 sweet corn are
currently cultivated for human and animal consumption in the EU.
The
charges follow a long struggle for justice by a German farmer whose
dairy cattle suffered mysterious illnesses and deaths after eating Bt
176. They were grown on his farm as part of authorised field tests
during 1997 to 2002. By 2000, his cows were fed exclusively on Bt 176,
and soon illnesses started to emerge. He was paid 40 000 euros by
Syngenta as partial compensation for 5 dead cows, decreased milk yields,
and vet costs (see [2] Cows ate GM Maize and Died, SiS 21).
During a civil lawsuit brought against the
company by the farmer however, Syngenta refused to admit that its GM
corn was the cause, claiming no knowledge of harm. The case was
dismissed and Gloeckner remained thousands of euros in debt.
Gloeckner
continued to lose cows and many more had to be put down due to serious
illnesses, compelling him to stop using GM feed from 2002. He approached
the Robert Koch Institute and Syngenta to conduct a full investigation.
However, only one cow was ever analysed and the data are still
unavailable to the public. Unsurprisingly, no causal relationship
between the GM feed and deaths was determined; and there is still no
explanation for the deaths.
But
in 2009, the farmer learned of a feeding study allegedly commissioned
by Syngenta in 1996 that
resulted in four cows dying in two days. The trial was abruptly
terminated. Now Gloeckner, along with a German group called Bündnis
Aktion Gen-Klage and another farmer turned activist Urs Hans, have
brought Syngenta to the criminal court to face charges of withholding
knowledge of the US trial, which makes the company liable for the
destruction of the farmer’s 65 cows. Syngenta is also charged with the
deaths of cattle in the US trial and on Gloeckner’s farm, which should
have been registered as “unexpected occurrences”. Most seriously, the
German head of Syngenta Hans-Theo Jahmann, is charged for withholding
knowledge of the US study from the judge and from Gloecker in the
original civil court case.
Gloecker’s cows not alone
This
is by no means the only account of mysterious deaths associated with Bt
GM feed. In India where livestock are left to graze on post-harvest
cotton, thousands of livestock deaths have been recorded in different
villages across central India where Bt cotton is grown (see [3] Mass Deaths of Sheep Grazing on Bt Cotton, SiS 30).
Shepherds’ own observations and post-mortem analysis carried out in the
laboratory revealed abnormal liver, enlarged bile ducts and black
patches in the intestine. The shepherds said that the sheep became
“dull/depressed” after 2-3 days of grazing, started coughing with nasal
discharge and developed red lesions in the mouth, became bloated and
suffered blackish diarrhoea, and sometimes
passed red urine. Death occurred within 5-7 days of grazing. Sheep from
young lambs to adults of 1.5-2 years were affected. One shepherd
reported getting diarrhoea from eating the meat of an affected sheep.
The vets declared that the toxicity could be due to the Bt toxin but
this could not be proven as results were confounded by additional
pesticides used on the fields. The shepherds were however, advised
against letting the sheep graze on any more Bt cotton plants.
Philippine
villagers living around Bt Maize fields have also suffered deaths and
similar illnesses of fever, respiratory, intestinal and skin problem
(see [4] GM ban long overdue, five deaths and dozens ill in the Philippines, SiS 29).
Five mortalities were reported in 2003 and subsequently, 38
individuals had their blood analysed and all were positive for
antibodies specific to Cry1Ab, suggesting an immune reaction to the
toxin. As is often the case, intimidation and denial by government
officials meant that there were no further investigations into the
matter.
Cause of deaths unknown
There
is still no explanation provided by the authorities as to the cause of
death of Gloeckner’s cows. The biotech industry claims that Bt toxins
are quickly digested in the stomach and are only effective in insect
target species. However, a recent study has found the toxin in the blood
of over 80 %
of women and their unborn children tested in Canada [5]. Because
naturally existing Bt toxins from the soil bacterium have been used for a
long time, long-term toxicology and health risk assessments on Bt
proteins in GM crops were not done. However, there are important
differences between the naturally produced toxins that can be washed off
the crops, as opposed to genetically modified toxins that are part and
parcel of the GM crop. Independent studies have shown that basing health
assessments on flawed scientific assumptions is not only arrogant, but
foolish.
Scientific
studies dating from the 1990s have identified Bt toxins as potent
immunogens, with Cry1Ac inducing immune responses in mice similar to the
cholera toxin [6]. Farm workers dealing with Bt cotton have
consistently reported allergic responses requiring hospitalisation in
some cases (see
[7] More Illnesses Linked to Bt Crops, SiS 30).
Binding of Cry1Ac to the intestine of mice has been shown, with
concomitant diarrhoea symptoms [8]. A meta-analysis of 3 month feeding
studies in laboratory animals found that Bt maize led to changes in
blood protein levels indicative of abnormal liver metabolism (see [9] GM Feed Toxic, Meta-Analysis Confirms, SiS 52). A recent study finds Cry1Ab toxic to human kidney cells, causing cell death at low doses (see [10] Bt Toxin Kills Human Kidney
Cells, SiS52).
|
Working to effect policy change for clean, organic food production planet-wide. Linking legislation, education, community and advocacy for Clean Food Earth.
Thursday, June 14, 2012
CRIMINAL CHARGES IN DEATHS LINKED TO Bt CORN COVER-UPS
THE GMO LABELING QUEST IS ON IN CALIFORNIA!
GMO labeling victory! Measure accepted onto California ballot; now the real battle begins.
As
many of you might know, if the ballot measure passes in CA in November we have
a real chance of that moving throughout the country. Everyone would then know
if GMO food was in a product or in the produce or meat departments. We could
have a choice.
by Mike Adams, the Health
Ranger, NaturalNews Editor
(NaturalNews) In this breaking news for the food-conscious community, the California Secretary of State has just announced that the GMO labeling ballot measure has met and exceeded the requirements to be placed on the November ballot. (http://www.sos.ca.gov/admin/ press-releases/2012/db12-068. pdf)
and (http://www.labelgmos.org/we_ made_it_on_the_ballot)
This measure, which has been strongly pushed by the Organic Consumers Association, the Institute for Responsible Technology, and a large number of dedicated volunteers and donors, would require genetically engineered ingredients to be indicated on food labels. This is an honest labeling issue that would allow consumers to make informed decisions about what they choose to purchase and consume.
504,760 signatures were needed to qualify for the November ballot, and the GMO labeling signature effort has greatly exceeded this number. Tremendous thanks are due to all those who fought for this honest labeling initiative. NaturalNews has consistently covered this issue from day one, and has helped drive significant awareness and funds to this GMO labeling effort.
A passage of this initiative could spell the end of GMOs in America, as food producers already know that if given a choice, 90+ percent of consumers would choose to avoid genetically engineered food. For this reason, food producers would be forced to switch to non-GMO sources for their food ingredients. This, in turn, would see a near collapse of GM seeds being planted in fields across America.
(NaturalNews) In this breaking news for the food-conscious community, the California Secretary of State has just announced that the GMO labeling ballot measure has met and exceeded the requirements to be placed on the November ballot. (http://www.sos.ca.gov/admin/
This measure, which has been strongly pushed by the Organic Consumers Association, the Institute for Responsible Technology, and a large number of dedicated volunteers and donors, would require genetically engineered ingredients to be indicated on food labels. This is an honest labeling issue that would allow consumers to make informed decisions about what they choose to purchase and consume.
504,760 signatures were needed to qualify for the November ballot, and the GMO labeling signature effort has greatly exceeded this number. Tremendous thanks are due to all those who fought for this honest labeling initiative. NaturalNews has consistently covered this issue from day one, and has helped drive significant awareness and funds to this GMO labeling effort.
A passage of this initiative could spell the end of GMOs in America, as food producers already know that if given a choice, 90+ percent of consumers would choose to avoid genetically engineered food. For this reason, food producers would be forced to switch to non-GMO sources for their food ingredients. This, in turn, would see a near collapse of GM seeds being planted in fields across America.
The disinfo war begins
Of course, Monsanto, DuPont, Big
Agriculture and the food industry don't want consumers to know what's in their
food. They profit when consumers are kept in the dark, and they will spend
tens of millions of dollars to spread disinformation about this initiative in
order to influence California voters to vote it
down.
Thus, the next great battle begins: The battle for voting YES on the ballot measure. Expect NaturalNews and all the same allies who advocated the ballot measure to now shift gears and start educating voters to support the ballot measure.
This initiative will be won on the internet. It is the website articles, Facebook posts, tweets and emails that will educate consumers to vote YES on this measure. Please join NaturalNews in this effort to achieve victory in November in California because it has global implications. If we can defeat Monsanto at the ballot in November, we will be one step closer to eliminating dangerous GM crops altogether.
Stay tuned to NaturalNews for more coverage of this crucial issue. We have won a major battle, but an even larger one awaits us in November.
Personally, I don't care who you vote for when it comes to President, as the candidates are virtually identical in their policies. But voting on this GMO ballot measure is the real reason to get out and vote. This is something that was written by the People, advocated by the People, and its passage will help protect the People from greed-driven corporations that sell poison and call it food.
It's time to end GMOs across America. If you're a California voter, vote YES on GMO labeling in November. Spread the word. Stay tuned to NaturalNews for more grassroots activism on this issue.
Victory against GMOs is within reach!
Thus, the next great battle begins: The battle for voting YES on the ballot measure. Expect NaturalNews and all the same allies who advocated the ballot measure to now shift gears and start educating voters to support the ballot measure.
This initiative will be won on the internet. It is the website articles, Facebook posts, tweets and emails that will educate consumers to vote YES on this measure. Please join NaturalNews in this effort to achieve victory in November in California because it has global implications. If we can defeat Monsanto at the ballot in November, we will be one step closer to eliminating dangerous GM crops altogether.
Stay tuned to NaturalNews for more coverage of this crucial issue. We have won a major battle, but an even larger one awaits us in November.
Personally, I don't care who you vote for when it comes to President, as the candidates are virtually identical in their policies. But voting on this GMO ballot measure is the real reason to get out and vote. This is something that was written by the People, advocated by the People, and its passage will help protect the People from greed-driven corporations that sell poison and call it food.
It's time to end GMOs across America. If you're a California voter, vote YES on GMO labeling in November. Spread the word. Stay tuned to NaturalNews for more grassroots activism on this issue.
Victory against GMOs is within reach!
Wednesday, June 13, 2012
FOR FOODIES - AND - ANYONE WHO EATS FOOD
Food and Technology
FRIENDS OF THE EARTH
Our farms and food are one of our most important connections to our environment. Yet as corporate agribusiness expands its control over our agricultural system and increasingly uses toxic chemicals and risky technologies to produce our food, our environment and health are threatened as is our ability to produce food sustainably.
Our farms and food are one of our most important connections to our environment. Yet as corporate agribusiness expands its control over our agricultural system and increasingly uses toxic chemicals and risky technologies to produce our food, our environment and health are threatened as is our ability to produce food sustainably.
Friends of the Earth is leading the charge to ensure our food system
is just and sustainable. The campaigns within our food and technology
project also pressure governments to embrace the safe and precautionary
management of emerging technologies, including nanotechnology and
synthetic biology, which are appearing in more consumer products such as
food, cosmetics and sunscreens each year.
Genetic engineering
We are working to keep genetically engineered "frankenfish" -- which
would be the first genetically engineered animal approved for human
consumption -- off of grocery store shelves.
Read more
Nanotechnology
We advocate for policies to protect the public from the risks posed
by the increasing use of nanomaterials in cosmetics, sunscreens and a
plethora of other consumer products.
Read more
Synthetic biology
We are pushing for proper government oversight of synthetic biology
-- a largely unregulated and rapidly developing biotechnology that
involves engineering new organisms from scratch.
Read more
Gene patents
We
are working to ban the patenting of human genes, which unjustly give
corporations control over research and potentially life-saving tests and
treatments drawn from these fundamental building blocks of life.
Read more
SOURCE: http://www.foe.org/projects/food-and-technology
RACTOPAMINE FED TO 60-80% OF U.S. PIGS. EVER HEARD OF IT?
Dispute Over Drug in Feed Limiting US Meat Exports
Updated on March 23: The FDA on March
14 issued a statement in response to this report, saying it had reviewed
its previously published adverse drug effect numbers on ractopamine.
After excluding reports of ineffectiveness, meat abnormalities and
fertility abnormalities, it said the number of animals with reports of
adverse effects was 160,917. The story reflects this recent analysis by
the FDA.
Updated on Feb. 22: A clarification to
the Jan. 25, 2012, story “Dispute over Drug in Feed, Limiting US
Exports” has been issued, making clear that the adverse drug effects
for ractopamine were reported to the FDA. The story adds that the FDA
says such data do not establish that the drug caused these effects.
A drug used to keep pigs lean and boost their growth is jeopardizing
the nation’s exports of what once was known as “the other white meat.”
Held up at Codex. Read our exclusive coverage here.
The drug, ractopamine hydrochloride, is fed to pigs and other animals
right up until slaughter and minute traces have been found in meat. The
European Union, China, Taiwan and many others have banned its use,
citing concerns about its effect on human health, limiting U.S. meat
exports to key markets.
Although few Americans outside of the livestock industry have ever
heard of ractopamine, the feed additive is controversial. Fed to an
estimated 60 to 80 percent of pigs in the United States, it has resulted
in more reports of sickened or dead pigs than any other livestock drug
on the market, an investigation of Food and Drug Administration records
shows.
Growing concern over sick animals in the nation’s food supply sparked
a California law banning the sale and slaughter of livestock unable to
walk, but that law was struck down by the Supreme Court Monday. Meat
producers had sued to overturn California’s ban, arguing that the state
could not supercede federal rules on meat production. The court agreed.
The FDA, which regulates livestock drugs in the United States, deemed
ractopamine safe 13 years ago and approved it, setting a level of
acceptable residues in meat. Canada and 24 other countries approved the
drug as well.
U.S. trade officials are now pressing more countries to accept meat
from animals raised on ractopamine — a move opposed by China and the EU.
Resolving the impasse is a top agricultural trade priority for the
Obama administration, which is trying to boost exports and help revive
the economy, trade officials say.
U.S. exports of beef and pork are on track to hit $5 billion each for
the first time, the U.S. Meat Export Federation estimates. Pork exports
to China quadrupled from 2005 to 2010 to $463 million but are still
only 2-3 percent of the market.
“China is a potentially huge market for us,” said Dave Warner, spokesman for the National Pork Producers Council.
Part of a class of drugs called beta-agonists, ractopamine mimics
stress hormones, making the heart beat faster and relaxing blood
vessels. Some beta-agonists are used to treat people with asthma or
heart failure, but ractopamine has not been proposed for human use.
In animals, ractopamine revs up production of lean meat, reducing
fat. Pigs fed the drug in the last weeks of their life produce an
average of 10 percent more meat, compared with animals on the same
amount of feed that don’t receive the drug. That raises profits by $2
per head, according to the drug’s manufacturer, Elanco, a division of
Eli Lilly. It sells the drug under the brand name Paylean.
Ractopamine leaves animals’ bodies quickly, with pig studies showing
about 85 percent excreted within a day. But low levels of residues can
still be detected in animals more than a week after they’ve consumed the
drug.
Testing for Drug Residues in Meat is Limited in U.S.
The U.S. Department of Agriculture’s Food Safety and Inspection Service,
responsible for the safety of the meat, poultry, and processed egg supply, runs
a National Residue Program to ensure that widely-used veterinary drugs, like growth-
promoters and antibiotics, do not end up in the nation’s food supply.
Though ractopamine is widely used in pigs and cattle, testing for ractopamine
residues in food animals is limited.
Last year, for example, no tests were conducted on 22 billion pounds of pork
produced in the United States; 712 samples were taken from 26 billion pounds of
beef but the results have not yet been released.
Between 2007 and 2009, the testing program detected ractopamine in a total of 20
pork and 7 beef samples — all below the safe residue limits set by the U.S. Food and
Drug Administration, the agency charged with overseeing veterinary drugs.
Though the drug has been approved for use in turkeys since 2008, to date there has
been no government testing for ractopamine residues.
Some scientists have raised issue with the general lack of research into the impact of
veterinary drugs on human health.
“There’s very little data on the low levels of veterinary drugs people are exposed to,”
said Keeve Nachman, a scientist who directs the Farming for the Future program at
the Johns Hopkins School of Public Health in Baltimore. “We don’t know much about
the toxicological significance of these exposures, and no one is really looking.”
With tightening budgets—and a new focus on additional strains of E. coli as well as
stricter poultry standards—food safety resources at USDA have been shifted away
from testing chemical and drug residues, according to FSIS officials.
“The reality is that resources are scarce,” said one FSIS official. “We are sometimes
asked to reduce the number of samples that we take.”
- Helena Bottemiller
responsible for the safety of the meat, poultry, and processed egg supply, runs
a National Residue Program to ensure that widely-used veterinary drugs, like growth-
promoters and antibiotics, do not end up in the nation’s food supply.
Though ractopamine is widely used in pigs and cattle, testing for ractopamine
residues in food animals is limited.
Last year, for example, no tests were conducted on 22 billion pounds of pork
produced in the United States; 712 samples were taken from 26 billion pounds of
beef but the results have not yet been released.
Between 2007 and 2009, the testing program detected ractopamine in a total of 20
pork and 7 beef samples — all below the safe residue limits set by the U.S. Food and
Drug Administration, the agency charged with overseeing veterinary drugs.
Though the drug has been approved for use in turkeys since 2008, to date there has
been no government testing for ractopamine residues.
Some scientists have raised issue with the general lack of research into the impact of
veterinary drugs on human health.
“There’s very little data on the low levels of veterinary drugs people are exposed to,”
said Keeve Nachman, a scientist who directs the Farming for the Future program at
the Johns Hopkins School of Public Health in Baltimore. “We don’t know much about
the toxicological significance of these exposures, and no one is really looking.”
With tightening budgets—and a new focus on additional strains of E. coli as well as
stricter poultry standards—food safety resources at USDA have been shifted away
from testing chemical and drug residues, according to FSIS officials.
“The reality is that resources are scarce,” said one FSIS official. “We are sometimes
asked to reduce the number of samples that we take.”
- Helena Bottemiller
While the Department of Agriculture has found traces of ractopamine
in American beef and pork, they have not exceeded levels the FDA has
determined are safe.
But because countries like China and Taiwan have no safety threshold,
traces of the drug have led to rejection of some U.S. meat shipments.
The EU requires U.S. exporters to certify their meat is
ractopamine-free, and China requires a similar assurance for pork.
Some U.S. food companies also avoid meat produced with the feed
additive, including Chipotle restaurants, meat producer Niman Ranch and
Whole Foods Markets.
The FDA ruled that ractopamine was safe and approved it for pigs in
1999, for cattle in 2003 and turkeys in 2008. As with many drugs, the
approval process relied on safety studies conducted by the drug-maker —
studies that lie at the heart of the current trade dispute.
Elanco mainly tested animals — mice, rats, monkeys and dogs — to
judge how much ractopamine could be safely consumed. Only one human
study was used in the safety assessment by Elanco, and among the six
healthy young men who participated, one was removed because his heart
began racing and pounding abnormally, according to a detailed evaluation
of the study by European food safety officials.
When Elanco studied the drug in pigs for its effectiveness, it
reported that “no adverse effects were observed for any treatments.” But
within a few years of Paylean’s approval, the company received hundreds
of reports of sickened pigs from farmers and veterinarians, according
to records from the FDA’s Center for Veterinary Medicine.
USDA meat inspectors also reported an increase in the number of
“downer pigs” — lame animals unable to walk — in slaughter plants. As a
result of the high number of adverse reactions, the FDA requested Elanco
add a warning label to the drug, and it did so in 2002.
The company also received a warning letter from the FDA that year for
failing to disclose all data about the safety and effectiveness of the
drug.
Since the drug was introduced, more than 160,000 pigs taking
ractopamine were reported to have suffered adverse effects, as of March
2011, according to a review of FDA records. The drug has triggered more
adverse reports in pigs than any other animal drug on the market. Pigs
suffered from hyperactivity, trembling, broken limbs, inability to walk
and death, according to FDA reports released under a Freedom of
Information Act request. The FDA, however, says such data do
not establish that the drug caused these effects.
“I’ve personally seen people overuse the drug in hogs and cattle,”
said Temple Grandin, a professor at Colorado State University and animal
welfare expert. “I was in a plant once where they used too much
ractopamine and the pigs were so weak they couldn’t walk. They had five
or six people just dedicated to handling the lame pigs.”
But she noted that producers have since scaled back use in response to the rash of illnesses.
“Our company takes adverse event reporting very seriously and is
overly inclusive on the information we submit to ensure we’re meeting
all requirements,” Elanco spokeswoman Colleen Par Dekker said. She said
the label change in 2002 resulted from an ongoing process of evaluating
adverse effects of the drug, adding that an industry trend towards
heavier pigs contributed to rising numbers of lame animals in this
period.
By 2003, with ractopamine rolling out across the livestock industry,
U.S. trade officials began pressing to open world markets for meat
produced with the feed additive. Their effort focused on a relatively
obscure corner of the trade world — the U.N.’s Codex Alimentarius
Commission, which sets global food-safety standards.
Setting a Codex standard for ractopamine would strengthen
Washington’s ability to challenge other countries’ meat import bans at
the World Trade Organization.
The issue has reached the last step in Codex’s approval process, but
since 2008 the commission has been deadlocked over one central question:
What, if any, level of ractopamine is safe in meat?
The EU and China, which together produce and consume about 70 percent
of the world’s pork, have blocked the repeated efforts of U.S. trade
officials to get a residue limit. European scientists sharply questioned
the science backing the drug’s safety, and Chinese officials were
concerned about higher residues in organ meats, which are consumed in
China.
“The main problem for us is that the safety of the product could not
be supported with the data,” said Claudia Roncancio-Peña, a scientist
who led the European food safety panel studying the drug.
U.S. trade officials say China wants to limit competition from U.S.
companies, and the EU does not want to risk a public outcry by importing
meat raised with growth-promoting drugs, which are illegal there.
The issue also has strained the U.S.-Taiwan trade relationship, since
Taiwan -– the sixth-largest market for U.S. beef and pork –- began
testing for ractopamine last year. It found traces in American beef and
pork and pulled meat from store shelves, according to local press
reports.
In the U.S., residue tests for ractopamine are limited. In 2010, for
example, the U.S. did no tests on 22 billion pounds of pork; 712 samples
were taken from 26 billion pounds of beef. Those results have not yet
been released.
This article first appeared on msnbc.com. Interested in syndication? Contact us at info@thefern.org
SOURCE: http://thefern.org/2012/01/dispute-over-drug-in-feed-limiting-u-s-meat-exports/ EVEN TINY TRACES OF CHEMICALS FROM FOOD WRAPPERS HAVING MASSIVE HEALTH IMPACTS
If Food’s in Plastic, What’s in the Food?
In a study published last year in the journal Environmental Health
Perspectives, researchers put five San Francisco families on a three-day
diet of food that hadn’t been in contact with plastic. When they
compared urine samples before and after the diet, the scientists were
stunned to see what a difference a few days could make: The
participants’ levels of bisphenol A (BPA), which is used to harden
polycarbonate plastic, plunged – by two-thirds, on average – while those
of the phthalate DEHP, which imparts flexibility to plastics, dropped
by more than half.
The findings seemed to confirm what many experts suspected: Plastic
food packaging is a major source of these potentially harmful chemicals,
which most Americans harbor in their bodies. Other studies have shown
phthalates (pronounced THAL-ates) passing into food from processing
equipment and food-prep gloves, gaskets and seals on non-plastic
containers, inks used on labels – which can permeate packaging – and
even the plastic film used in agriculture.
The government has long known that tiny amounts of chemicals used to
make plastics can sometimes migrate into food. The Food and Drug
Administration regulates these migrants as “indirect food additives” and
has approved more than 3,000 such chemicals for use in food-contact
applications since 1958. It judges safety based on models that estimate
how much of a given substance might end up on someone’s dinner plate. If
the concentration is low enough (and when these substances occur in
food, it is almost always in trace amounts), further safety testing
isn’t required.
Meanwhile, however, scientists are beginning to piece together data
about the ubiquity of chemicals in the food supply and the cumulative
impact of chemicals at minute doses. What they’re finding has some
health advocates worried.
This is “a huge issue, and no [regulator] is paying attention,” says
Janet Nudelman, program and policy director at the Breast Cancer Fund, a
nonprofit that focuses on the environmental causes of the disease. “It
doesn’t make sense to regulate the safety of food and then put the food
in an unsafe package.”
A complicated issue
How common are these chemicals? Researchers have found traces of
styrene, a likely carcinogen, in instant noodles sold in polystyrene
cups. They’ve detected nonylphenol – an estrogen-mimicking chemical
produced by the breakdown of antioxidants used in plastics – in apple
juice and baby formula. They’ve found traces of other hormone-disrupting
chemicals in various foods: fire retardants in butter, Teflon
components in microwave popcorn, and dibutyltin – a heat stabilizer for
polyvinyl chloride – in beer, margarine, mayonnaise, processed cheese
and wine. They’ve found unidentified estrogenic substances leaching from
plastic water bottles.
Is It Possible to Build a Safer Plastic Package?
A growing number of companies are using “green chemistry” to create
new polymers and additives without known hazards. But Mike Usey, CEO of a
small Texas start-up called Plastipure, says there’s a simpler
solution: Find the existing plastic resins and additives that don’t
interfere with natural hormones. There are plenty out there, he says,
but identifying them is complicated because one type of plastic can be
formulated in many different ways, making some brands or grades safer
than others.
Plastipure was started in 2000 by George Bittner, a University of Texas neurobiologist who developed analytic methods to systematically recognize synthetic chemicals that are not estrogenically active, or “EA-free,” in the company parlance. They don’t, in other words, mimic estrogens naturally produced by the body. “We’ve taken thousands and thousands of tests on materials and chemicals and additives, so we know now what is commercially used that is EA-free and what is not,” says Usey. Their first product, released in 2008, was a water bottle they proclaimed to be entirely EA-free.
In 2011, Plastipure scientists published a study in which they tested some 500 plastic packages and products. Their results showed 92 percent were estrogenically active, even products that claimed to be BPA-free. Although the research was “obviously commercially motivated, I think they raised a very legitimate issue,” says Bill Pease, a toxicologist for GoodGuide, a group that rates the health and environmental safety of consumer products. In 2011, the National Science Foundation awarded Plastipure a $650,000 grant to further develop its EA-free technology.
But Usey says while consumers may like the idea of an EA-free plastic, it’s been a tough sell, even to well-meaning food companies. Despite interest, no one wants to be the first to adopt a new type of package. “Everybody wants … to be second,” he says with a sigh of frustration. “The companies’ first concern is liability – if we put something out that we say is safer, are we admitting what we did before is unsafe?”
Plastipure was started in 2000 by George Bittner, a University of Texas neurobiologist who developed analytic methods to systematically recognize synthetic chemicals that are not estrogenically active, or “EA-free,” in the company parlance. They don’t, in other words, mimic estrogens naturally produced by the body. “We’ve taken thousands and thousands of tests on materials and chemicals and additives, so we know now what is commercially used that is EA-free and what is not,” says Usey. Their first product, released in 2008, was a water bottle they proclaimed to be entirely EA-free.
In 2011, Plastipure scientists published a study in which they tested some 500 plastic packages and products. Their results showed 92 percent were estrogenically active, even products that claimed to be BPA-free. Although the research was “obviously commercially motivated, I think they raised a very legitimate issue,” says Bill Pease, a toxicologist for GoodGuide, a group that rates the health and environmental safety of consumer products. In 2011, the National Science Foundation awarded Plastipure a $650,000 grant to further develop its EA-free technology.
But Usey says while consumers may like the idea of an EA-free plastic, it’s been a tough sell, even to well-meaning food companies. Despite interest, no one wants to be the first to adopt a new type of package. “Everybody wants … to be second,” he says with a sigh of frustration. “The companies’ first concern is liability – if we put something out that we say is safer, are we admitting what we did before is unsafe?”
Finding out which chemicals might have seeped into your groceries is
nearly impossible, given the limited information collected and disclosed
by regulators, the scientific challenges of this research and the
secrecy of the food and packaging industries, which view their
components as proprietary information. Although scientists are learning
more about the pathways of these substances – and their potential effect
on health – there is an enormous debate among scientists, policymakers
and industry experts about what levels are safe.
The issue is complicated by questions about cumulative exposure, as
Americans come into contact with multiple chemical-leaching products
every day. Those questions are still unresolved, says Linda Birnbaum,
director of the National Institute of Environmental Health Science, part
of the National Institutes of Health. Still, she said, “we do know that
if chemicals act by the same pathway that they will act in an additive
manner” – meaning that a variety of chemicals ingested separately in
very small doses may act on certain organ systems or tissues as if they
were a single cumulative dose.
The American Chemistry Council says there is no cause for concern.
“All materials intended for contact with food must meet stringent FDA
safety requirements before they are allowed on the market,” says
spokeswoman Kathryn Murray St. John. “Scientific experts review the full
weight of all the evidence when making such safety determinations.”
Hard to measure
When it comes to food packaging and processing, among the most
frequently studied agents are phthalates, a family of chemicals used in
lubricants and solvents and to make polyvinyl chloride pliable. (PVC is
used throughout the food processing and packaging industries for such
things as tubing, conveyor belts, food-prep gloves and packaging.)
Because they are not chemically bonded to the plastic, phthalates can
escape fairly easily. Some appear to do little harm, but animal studies
and human epidemiological studies suggest that one phthalate, called
DEHP, can interfere with testosterone during development. Studies have
associated low-dose exposure to the chemical with male reproductive
disorders, thyroid dysfunction and subtle behavioral changes.
But measuring the amount of phthalates that end up in food is
notoriously difficult. Because these chemicals are ubiquitous, they
contaminate equipment in even purportedly sterile labs.
In the first study of its kind in the United States, Kurunthachalam
Kannan, a chemist at the New York State Department of Health, and Arnold
Schecter, an environmental health specialist at the University of Texas
Health Science Center, have devised a protocol to analyze 72 different
grocery items for phthalates. Schecter won’t reveal the results before
they’re published – later this year, he hopes – except to say he found
DEHP in many of the samples tested.
Perhaps the most controversial chemical in food packaging is BPA,
which is chiefly found in the epoxy lining of food cans and which mimics
natural estrogen in the body. Many researchers have correlated low-dose
exposures to BPA with later problems such as breast cancer, heart
disease and diabetes. But other studies have found no association.
Canada declared BPA toxic in October 2010, but industry and regulators
in the United States and in other countries maintain that health
concerns are overblown.
Last month, the FDA denied a petition to ban the chemical, saying in a
statement that while “some studies have raised questions as to whether
BPA may be associated with a variety of health effects, there remain
serious questions about these studies, particularly as they relate to
humans and the public health impact.”
The fact that a plastic bottle or bag or tub can leach chemicals
doesn’t necessarily make it a hazard to human health. Indeed, to the
FDA, the key issue isn’t whether a chemical can migrate into food, but
how much of that substance consumers might ingest.
If simulations and modeling studies predict that a serving contains
less than 0.5 parts of a suspect chemical per billion – equivalent to
half a grain of salt in an Olympic-size swimming pool – FDA’s guidance
does not call for any further safety testing. On the premise that the
dose makes the poison, the agency has approved a number of potentially
hazardous substances for food-contact uses, including phosphoric acid,
vinyl chloride and formaldehyde.
Emerging science
But critics now question that logic. For one thing, it doesn’t take
into account the emerging science on chemicals that interfere with
natural hormones and might be harmful at much lower doses than has been
thought to cause health problems. Animal studies have found that
exposing fetuses to doses of BPA below the FDA’s safety threshold can
affect breast and prostate cells, brain structure and chemistry, and
even later behavior.
According to Jane Muncke, a Swiss researcher who has reviewed
decades’ worth of literature on chemicals used in packaging, at least 50
compounds with known or suspected endocrine-disrupting activity have
been approved as food-contact materials.
“Some of those chemicals were approved back in the 1960s, and I think
we’ve learned a few things about health since then,” says Thomas
Neltner, director of a Pew Charitable Trusts project that examines how
the FDA regulates food additives. “Unless someone in the FDA goes back
and looks at those decisions in light of the scientific developments in
the past 30 years, it’s pretty hard to say what is and isn’t safe in the
food supply.”
FDA spokesman Doug Karas in an e-mail interview said that before
approving new food-contact materials, the agency investigates the
potential for hormonal disruption “when estimated exposures suggest a
need.” But FDA officials don’t think the data on low-dose exposures
prove a need to revise that 0.5 ppb exposure threshold or reassess
substances that have already been approved.
Another criticism is that the FDA doesn’t consider cumulative dietary
exposure. “The risk assessments have been done only one chemical at a
time, and yet that’s not how we eat,” Schecter notes. (Karas counters
that “there currently are no good methods to assess these types of
effects.”)
“The whole system is stacked in favor of the food and packaging
companies and against the protecting of public health,” Nudelman, of the
Breast Cancer Fund, says. She and others are concerned that the FDA
relies on manufacturers to provide migration data and preliminary safety
information, and that the agency protects its findings as confidential.
So consumers have no way of knowing what chemicals, and in what
amounts, they are putting on the table every day.
It’s not just consumers who lack information. The companies that make
the food in the packages can face the same black box. Brand owners
often do not know the complete chemical contents of their packaging,
which typically comes through a long line of suppliers.
What’s more, they might have trouble getting answers if they ask.
Nancy Hirshberg, vice president of natural resources at Stonyfield Farm,
describes how in 2010, the organic yogurt producer decided to launch a
multipack yogurt for children in a container made of PLA, a corn-based
plastic. Because children are particularly vulnerable to the effects of
hormone disrupters and other chemicals, the company wanted to ensure
that no harmful chemicals would migrate into the food.
Stonyfield was able to figure out all but 3 percent of the
ingredients in the new packaging. But when asked to identify that 3
percent, the plastic supplier balked at revealing what it considered a
trade secret. To break the impasse, Stonyfield hired a consultant who
put together a list of 2,600 chemicals that the dairy didn’t want in its
packaging. The supplier confirmed that none were in the yogurt cups,
and a third party verified the information.
Originally published by the Washington Post
EXTREME PRICE FOR "CHEAP" MEAT
Food has gotten cheaper — but at what cost?
By Tom Laskawy
How appropriate then that NPR’s Planet Money, as part of its Graphing America series, should look at how America’s food spending has changed over the last 30 years. The headline figure — the one Secretary of Agriculture Tom Vilsack (Former Monsanto Man -Clean Food Earth Woman) is proudest of — is that we spend just under 9 percent of our income on food, about 30 percent less than we did in 1982.
Despite the drop, our shopping baskets have stayed more or less the same — with one notable exception. Processed foods now take the lion’s share of our collective food spending — their share has doubled in the last 30 years. On a percentage basis, we’re spending about the same as we did back then on fruits and vegetables, dairy, bread, and even beverages. Spending on meat, however, has dropped by a third — some of that savings goes to other kinds of spending, of course, since overall food spending is down, but clearly some of the money formerly spent on meat has shifted to processed snacks, treats, and packaged foods.
In fact, while fruit and vegetable prices overall have increased faster than inflation (though Planet Money points out that certain items like apples, lettuce, and even tomatoes have defied that trend, at great cost to farm laborers) — it’s those meat prices that demonstrate the most shocking price drop.
Thank you, Smithfield, Tyson, and Cargill! Many will argue that this is a very positive development. Meat used to be a luxury good and is now readily available to many more people at more income levels. The problem, of course, is that the drop in retail price also represents a massive cost shift. As the meat industry consolidated, industrialized, and specialized, labor costs dropped — but rural unemployment soared.
Meanwhile, the environmental costs of livestock farming, which were manageable when fewer animals in smaller farms were distributed over larger areas, were shifted, too. And in ways that are both difficult to ignore and to address — we’ve polluted rivers with runoff from pork, dairy, and chicken operations, and created massive dead zones in bays and gulfs around the country.
There’s a human cost, too. Workers in the giant slaughterhouses that now dominate the meat industry labor in some of the worst workplace conditions in the country and are prone to illness and injury. Workers in the facilities where the animals are raised have also been pushed to the limit — mistreatment of animals appears to be all too common. Oh, and let’s not forget the human cost to consumers, as the tragedy that results from antibiotic-resistant infections and mass distribution of meat contaminated with deadly pathogens represents far more than unwelcome statistics.
And then there are the animals themselves. Animal welfare went out the window with industrialization; when animals are seen as widgets in a factory, they get treated as such. From the way the animals are bred — such as chickens with oversized breasts that are unable to walk — to the need to pump them full of antibiotics simply so they can survive the disease-ridden, stressful facilities in which they live, most farm animals’ lives are nasty, brutish, and short. (The philosophers among you might note the irony that these animals exist in the Hobbesian “state of nature” while at the same time in a completely artificial environment.)
I’d also feel better about this reduction in food spending if it didn’t coincide with the shift toward processed food and the onset of the obesity epidemic. We’re spending less for food, but we’re also clearly eating far worse. Researchers estimate that obesity now adds thousands of dollars to all Americans’ insurance premiums whether they’re obese or not. Kinda ruins the benefit of cheap food, doesn’t it? And as The New York Times reports, it’s an epidemic that hits low-income communities hardest and remains especially difficult to address.
And then there’s the fact that despite low prices, there are still so many damn hungry people in this country. Almost 50 million Americans are considered “food insecure” by the USDA, and food stamp use is higher than ever. In fact, the relentless focus on lowering food spending obscures the much larger problem — that middle class wages have stagnated over the same period. At the same time, health-care spending has increased radically — although that comes mostly in the form of companies paying more for workers’ insurance premiums rather than giving them raises.
So the next time you hear a government official or a corporate executive touting the benefits of an industrialized food system that allows Americans to spend less than ever on food, just remember: You get what you pay for.
Tom Laskawy is a founder and executive director of the Food & Environment Reporting Network and a contributing writer at Grist covering food and agricultural policy. His writing has also appeared in The American Prospect, Slate, The New York Times, and The New Republic. Follow him on Twitter.
SOURCE: http://grist.org/food/food-has-gotten-cheaper-but-at-what-cost/
NEVER BEEN TESTED - WANNA EAT IT OR- LABEL IT?
How California's GM Food Referendum May Change What America Eats
The vast majority of Americans want genetically modified food labelled. If California passes November's ballot, they could get it
Published on Wednesday, June 13, 2012 by The Guardian/UK
Last month, nearly 1 million signatures were delivered to county registrars throughout California calling for a referendum on the labeling of genetically engineered foods. If the measure, "The Right to Know Genetically Engineered Food Act",
which will be on the ballot in November, passes, California will become
the first state in the nation to require that GM foods be labeled as
such on the package.
This is not the first time that the issue has come up
in California. Several labeling laws have been drafted there, but none
has made it out of legislative committee. Lawmakers in states like
Vermont and Connecticut have also proposed labeling legislation, which
has gone nowhere in the face of stiff industry opposition. And the US
Congress has likewise seen sporadic, unsuccessful attempts to mandate GM
food labeling since 1999.
What makes the referendum in California different is that, for the
first time, voters and not politicians will be the ones to decide. And
this has the food industry worried. Understandably so, since only one in
four Americans is convinced that GMOs are "basically safe", according to a survey conducted by the Mellman Group, and a big majority wants food containing GMOs to be labeled.
This is one of the few issues in America today that enjoys broad
bipartisan support: 89% of Republicans and 90% of Democrats want
genetically altered foods to be labeled, as they already are in 40
nations in Europe, in Brazil, and even in China. In 2007, then candidate
Obama latched onto this popular issue saying that he would push for
labeling – a promise the president has yet to keep.
In Europe, only 5% of food sold contains GMOs, a figure that continues to shrink.
In the US, by contrast, an estimated 70% of the products on supermarket
shelves include at least traces of genetically engineered crops –
mostly, corn and soy byproducts and canola oil, which are ingredients in
many of America's processed foods.
Given their unpopularity with consumers, labeling "Frankenfoods"
would undoubtedly hurt sales, possibly even forcing supermarkets to take
them off their shelves. In one survey, just over half of those polled said they would not buy food that they knew to be genetically modified.
In Europe, only 5% of food sold contains GMOs, a figure that continues to shrink.
In the US, by contrast, an estimated 70% of the products on supermarket
shelves include at least traces of genetically engineered crops –
mostly, corn and soy byproducts and canola oil, which are ingredients in
many of America's processed foods.
This makes the financial stakes for November's referendum vote huge.
California is not just America's leading agricultural state, but the
most populous state in the nation. If companies are made to change their
labels in California, they may well do so all over the country, rather
than maintain a costly two-tier packaging and distribution system.
Several hurdles will have to be overcome, however, before this
happens. The ballot initiative will face fierce opposition from the food
and biotech industries, which are expected to spend an estimated $60-100m on an advertising blitz
to convince Californians that labeling is unnecessary, will hurt
farmers, increase their food prices, and even contribute to world
hunger.
One lobbyist the corporations have hired to make this case is Tom Hiltachk, the head of the Coalition Against the Costly Food Labeling Proposition (CACFLP),
whose members include the Grocery Manufacturers Association (GMA),
Monsanto, BASF, Bayer, Dow and Syngenta, as well as several big food
processors and supermarket chains. Hiltachk is no stranger to the
shadowy world of industry front groups, according to Alexis Baden-Mayer,
political director of the Organic Consumers Association. The food activist reported on Alternet that:
"With a little help from his friends at Philip Morris and RJ Reynolds, he helped organize the Californians for Smokers' Rights group to fight anti-smoking initiatives in the 1980s and 1990s."
Also working to defeat the labeling initiative, according to Baden-Mayer, is the California Citizens Against Lawsuit Abuse (CALA),
which likewise receives big bucks from the tobacco industry and
assorted other corporations. The consumer watchdog group Public Citizen
says that CALA aims "to incite public scorn for the civil justice
system, juries and judges, and to pave the way for enactment of laws
immunizing corporations from liability for actions that harm consumers."
Whether lobbying groups like these will be able to convince famously
independent Californians to reject the labeling initiative in November
remains to be seen. But even if the referendum passes, the food industry
can be expected to challenge in court the state's right to mandate its
own labeling requirements – a function usually reserved for the Food and
Drug Administration (FDA), at the federal level.
The FDA's position on GMOs is that they are safe and essentially
equivalent nutritionally to conventionally grown food varieties. But
critics counter that the FDA has no way of knowing if this is true,
since crucial testing of GM foods has never been required by the agency,
and indeed, has not yet been conducted. Writes Dr Suzanne Wuerthele, a toxicologist with the US Environmental Protection Agency (EPA):
"We are confronted with the most powerful technology the world has ever known, and it is being rapidly deployed with almost no thought whatsoever to its consequences."
The concern is that genetic modification alters the proteins in foods
in ways that researchers do not yet fully understand. Substances that
have never existed before in nature are entering our food supply
untested. While researchers have not yet found a "smoking gun", which
would prove that GM foods as a class are dangerous, there are troubling
signs that they may be a factor in the recent epidemic of food
allergies. Soon after GM soy was introduced to the UK, for example, soy allergies escalated by 50%.
Rosa Rashall, a nutritionist in Garberville, California, who took
part in the petition campaign to get the labeling initiative on the
ballot, told the Redwood Times:
"We are all worried for a variety of reasons, from health effects to skyrocketing food sensitivities that have started to come about in the last 20 years. There has been an incredible 400% increase in food sensitivities that coincides pretty well with the unlabeled introduction of GMO food into the marketplace."
Critics also argue that agriculture's increasing dependence on GMOs
has coincided with a steep rise in toxic agrochemical use over the last
decade. A variety of GM corn sold by Monsanto was developed specifically
to withstand punishing doses of the company's bestselling herbicide,
Roundup.
Food scientists remain divided on the larger food safety
issue. Some say that there is no cause for alarm, while others cite the
allergy problem and also animal studies, like one published by the International Journal of Biological Sciences,
which showed high levels of kidney and liver failures (the two organs
of detoxification) in rats that were fed Monsanto GM corn. Monsanto's
biotech corn is designed to produce a pesticide in its cellular structure
that wards off insect pests. Nobody knows what effect this toxin will
have on the people who eat the flesh of livestock that are fed it.
The bottom line is that we can't be sure what the physiological
effects of consuming GM foods are until rigorous human trials are
conducted – which is not likely to happen anytime soon.
Californians aren't waiting until all of the scientific results are
in. And what they decide at the polling station in November may change
what the rest of us eat.
© 2012 Guardian News and Media Limited
Richard Schiffman is the author of two books and a former
journalist whose work has appeared in, amongst other outlets, the New
York Times and on a variety of National Public Radio shows including
Morning Edition and All Things Considered.
Source: http://www.commondreams.org/view/2012/06/13-9Tuesday, June 12, 2012
SAY NO TO 2,4-D AGENT ORANGE!!
Tell EPA: No on 2,4-D
In a recent action alert, we asked you to urge USDA NOT to approve Dow’s new, genetically engineered corn resistant to 2,4-D, part of the infamous Agent Orange used in Vietnam. Together, we sent USDA over 350,000 comments!
Today, we’re asking you to send the same message to the EPA.
While USDA directly controls the fate of the entire 2,4-D-resistant crop system, in this instance--in part because of the awareness you have already helped raise--EPA has decided to also play a role in determining whether and how 2,4-D can be sprayed on these new crops. EPA is currently considering Dow’s requests to permit use of 2,4-D on both GE corn and soybeans resistant to this herbicide.
EPA approval of 2,4-D use on Dow’s new GE crops would drive a massive increase in use of this toxic herbicide. This is bad for farmer and consumer health, the environment, and U.S. agriculture as whole.
In a recent action alert, we asked you to urge USDA NOT to approve Dow’s new, genetically engineered corn resistant to 2,4-D, part of the infamous Agent Orange used in Vietnam. Together, we sent USDA over 350,000 comments!
Today, we’re asking you to send the same message to the EPA.
While USDA directly controls the fate of the entire 2,4-D-resistant crop system, in this instance--in part because of the awareness you have already helped raise--EPA has decided to also play a role in determining whether and how 2,4-D can be sprayed on these new crops. EPA is currently considering Dow’s requests to permit use of 2,4-D on both GE corn and soybeans resistant to this herbicide.
EPA approval of 2,4-D use on Dow’s new GE crops would drive a massive increase in use of this toxic herbicide. This is bad for farmer and consumer health, the environment, and U.S. agriculture as whole.
Sunday, June 10, 2012
WHAT THE FRACK? BEANS, BEANS, THE PROFITABLE FRUIT...
Halliburton gets tripped up by Indian bean farmers*
By Philip Bump
Economics
101: supply and demand. The more supply in the market, the price of a
product drops. The more demand, prices rise. Demand leads to sales,
which reduces supply and forces prices higher and higher until either 1)
supply runs out or 2) prices drop demand.
This isn’t a theoretical or arcane concept. Here’s how that process played out just this week.
Last month, Reuters told the story of an unexpected economic windfall for farmers in India’s northern deserts. The seeds from guar beans,
which look like bean/pea hybrids and for which the region is the
primary source, can be processed to create a powdery gum. This gum is
used in a variety of products: ice cream, sauces — and the liquid
employed in hydraulic fracturing. Guar gum is an emulsifier, a
thickener. In the fracking process, it’s generally combined with
kerosene to create the fluid forced deep into shale deposits. (This video shows how the compound is made.)
As hydraulic fracturing has exploded (figuratively!) (so far!) in
America, so has demand for guar beans. Between 2011 and 2012, prices for
the beans shot up tenfold, prompting Indian authorities to investigate how the market was operating. The farmers had fewer concerns:
“Guar has changed my life,” said Shivlal, a guar farmer who made 300,000 rupees ($5,400) — five times more than his average seasonal income — from selling the beans he planted on five acres (two hectares) of sandy soil in Rajasthan state.
“Now, I have a concrete house and a color TV. Next season I will even try to grow guar on the roof.”
Demand and prices spiked. Until the market reached the point at which the demand cracks.
Earlier this week, Halliburton announced lower-than-expected profits for the second quarter of the year due to a shortage of Indian guar beans.
The giant oilfields services company attributed the bigger decline in its profit margins to a shortage of guar beans in India. … Halliburton has said the guar system can now account for as much as 30 percent of the overall fracking price.
“They’ve been passing along the cost incrementally, but because there’s been such a burst in pricing, it’s been hard to keep up with,” said Grant Fox, an analyst at Sterne, Agee & Leach.
It’s not clear what happens next. The Indian farmers — and the
company Vikas WSP, which has been passing out free guar seeds in an
effort to increase supply more rapidly — clearly hope to maintain the
bean’s popularity and price. Halliburton, meanwhile, is marketing CleanStim,
a non-guar-based fracking fluid “made with ingredients sourced from the
food industry.” (Please read the footnote provided: “Even though all
the ingredients are acquired from food suppliers, the CleanStim fluid
system should not be considered edible.” Good tip, guys!)
In the world’s most advanced economy, one in which transactions hinge
on microsecond gaps between online systems, a massive, multi-billion
dollar company still gets tripped up on how fast farmers in India can
grow beans.
Economic fundamentals at work.
* Alternate title — Guar: What is it good for?
SOURCE: http://grist.org/news/halliburton-gets-tripped-up-by-indian-bean-farmers/
ANOTHER MONSANTO FANSTASY ON DROUGHT RESISTANCE?
Monsanto’s Genetically-Modified “DroughtGard” Corn Barely a Drop in the Bucket
Report Finds Limited Prospects for Genetically Engineered Crops to Combat Drought and Conserve Water
Report by Union of Concerned Scientists
Published on Sunday, June 10, 2012 by Common Dreams
Published on Sunday, June 10, 2012 by Common Dreams
Monsanto’s new drought tolerant corn, DroughtGard, reduces crop
losses only modestly during moderate droughts, and will not reduce the
crop’s water requirements, according to a report released today by the
Union of Concerned Scientists (UCS). The report found that traditional
breeding and improved farming practices have done more to increase
drought tolerance, and that further improvements in genetic engineering
are unlikely to solve the drought problem in coming years.
“Farmers are always looking to reduce losses from drought, but the biotechnology industry has made little real-world progress on this problem,” said Doug Gurian-Sherman, a senior scientist with UCS’s Food & Environment Program and author of the report. “Despite many years of research and millions of dollars in development costs, DroughtGard doesn’t outperform the non-engineered alternatives.”
Agriculture accounts for about 70 percent of all water extracted from rivers and wells, making drought a serious and costly problem for farmers. An extreme drought is still plaguing Texas, triggering a record $5.2 billion in agricultural losses in 2011 alone. Monsanto’s new corn is not likely to provide any practical help under such conditions, even by the company’s guarded claims.
The report, High and Dry: Why Genetic Engineering is Not Solving Agriculture’s Drought Problem in a Thirsty World, found that during limited testing, DroughtGard—the only crop engineered for drought tolerance approved for commercial use—reduced crop losses by about 6 percent. By comparison, breeding and improved farming practices have increased drought tolerance by roughly 1 percent per year over the past several decades.
In terms of crop yields, DroughtGard will increase overall corn production by about 1 percent because it is likely to be of practical value on only about 15 percent of U.S. corn acreage. Breeding and improved farming practices increase corn production by about 1.5 to 2 percent annually.
“If we were to conduct an apples-to-apples comparison today, we’d find that breeding and improved farming practices have increased drought tolerance in corn about two to three times faster than DroughtGard,” said Gurian-Sherman. “Classical and newer forms of breeding are also far cheaper.”
DroughtGard is further handicapped by the fact that it will work well only under moderate drought conditions, and climate scientists predict that drought frequency and severity likely will increase in some regions as climate change worsens, Gurian-Sherman said. The fact that drought is not predicable also makes it difficult for farmers to decide whether it is worthwhile to buy DroughtGard seed prior to the growing season.
Finally, Monsanto’s advertising campaigns touted its intention to develop seeds that yield “more crop per drop,” but there is no evidence that DroughtGard will help the crops or farmers use water more efficiently. And the biotech industry’s pipeline for other water-efficient crops is virtually dry.
Congress and the U.S. Department of Agriculture can help farmers address droughts by substantially increasing support for public crop-breeding programs in the Farm Bill, Gurian-Sherman said. The Farm Bill also should fund research and offer incentives for farmers to adopt practices that improve drought tolerance such, as organic farming and similar methods that improve the soil’s ability to retain moisture.
“The fact that DroughtGard may provide modest drought tolerance is a small step forward for the industry, but it’s being outpaced by other methods,” said Gurian-Sherman. “More Farm Bill investments in public-sector classical breeding and water-saving farming practices would be more cost-effective for taxpayers and farmers, and as the scientific track record to date shows, will help farmers far more than genetic engineering.”
“Farmers are always looking to reduce losses from drought, but the biotechnology industry has made little real-world progress on this problem,” said Doug Gurian-Sherman, a senior scientist with UCS’s Food & Environment Program and author of the report. “Despite many years of research and millions of dollars in development costs, DroughtGard doesn’t outperform the non-engineered alternatives.”
Agriculture accounts for about 70 percent of all water extracted from rivers and wells, making drought a serious and costly problem for farmers. An extreme drought is still plaguing Texas, triggering a record $5.2 billion in agricultural losses in 2011 alone. Monsanto’s new corn is not likely to provide any practical help under such conditions, even by the company’s guarded claims.
The report, High and Dry: Why Genetic Engineering is Not Solving Agriculture’s Drought Problem in a Thirsty World, found that during limited testing, DroughtGard—the only crop engineered for drought tolerance approved for commercial use—reduced crop losses by about 6 percent. By comparison, breeding and improved farming practices have increased drought tolerance by roughly 1 percent per year over the past several decades.
In terms of crop yields, DroughtGard will increase overall corn production by about 1 percent because it is likely to be of practical value on only about 15 percent of U.S. corn acreage. Breeding and improved farming practices increase corn production by about 1.5 to 2 percent annually.
“If we were to conduct an apples-to-apples comparison today, we’d find that breeding and improved farming practices have increased drought tolerance in corn about two to three times faster than DroughtGard,” said Gurian-Sherman. “Classical and newer forms of breeding are also far cheaper.”
DroughtGard is further handicapped by the fact that it will work well only under moderate drought conditions, and climate scientists predict that drought frequency and severity likely will increase in some regions as climate change worsens, Gurian-Sherman said. The fact that drought is not predicable also makes it difficult for farmers to decide whether it is worthwhile to buy DroughtGard seed prior to the growing season.
Finally, Monsanto’s advertising campaigns touted its intention to develop seeds that yield “more crop per drop,” but there is no evidence that DroughtGard will help the crops or farmers use water more efficiently. And the biotech industry’s pipeline for other water-efficient crops is virtually dry.
Congress and the U.S. Department of Agriculture can help farmers address droughts by substantially increasing support for public crop-breeding programs in the Farm Bill, Gurian-Sherman said. The Farm Bill also should fund research and offer incentives for farmers to adopt practices that improve drought tolerance such, as organic farming and similar methods that improve the soil’s ability to retain moisture.
“The fact that DroughtGard may provide modest drought tolerance is a small step forward for the industry, but it’s being outpaced by other methods,” said Gurian-Sherman. “More Farm Bill investments in public-sector classical breeding and water-saving farming practices would be more cost-effective for taxpayers and farmers, and as the scientific track record to date shows, will help farmers far more than genetic engineering.”
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