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believe_it
QUOTE
http://fanaticcook.blogspot.com/2009/08/us...ic-biotech.html

Friday, August 21, 2009
USDA Argues For "Organic-Biotech"

Do you think that foods labeled "Organic" should be allowed to be made from genetically engineered ingredients? A report out of the USDA Foreign Agricultural Service is arguing that producers should be allowed to gain organic certification for biotech (genetically engineered) crops:





The Unexplored Potential of Organic-Biotech Production (pdf) broken link
USDA Foreign Agricultural Service, Italy
May 26, 2009

According to the Organic Consumers Association, the report above, "is part of a well-funded campaign coordinated by Monsanto and their governmental, corporate, and non-profit partners to legitimize a dangerous and untested technology."

"Organic-Biotech." If ever there was an oxymoron.

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The photo is from one of Barry Estabrook's (of Gourmet Magazine) columns, "GM Birth Control?" He describes an experiment where mice were fed Monsanto's genetically engineered corn (pictured). The mice "had fewer litters, fewer offspring, and more instances of complete infertility than those receiving a conventional diet."

Posted by Bix at 4:31 PM



QUOTE
http://www.organicconsumers.org/articles/article_18878.cfm

BREAKING NEWS FROM OCA EDITORS:

(August 29, 2009) -- After receiving thousands of letters from organic consumers, the USDA has pulled the following pro-GMO report from their Web site, explaining:

On May 26, 2009, the Foreign Agricultural Service (FAS) posted a Global Agriculture Information Network (GAIN) report titled, “The Unexplored Potential of Organic-Biotech Production.” This report should have been accompanied by a clear statement that the report does not represent the policy of the United States Government, and given this, the report has been removed from the agency’s Web site. It should be noted that USDA’s National Organic Program regulations exclude the use of genetically engineered organisms in organic production. Additionally, FAS has no role in the administration of the National Organic Program.


Full article at OCA link:
http://www.organicconsumers.org/articles/article_18878.cfm

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Google: The Unexplored Potential of Organic-Biotech Production
http://www.google.com/search?q=The+Unexplo...amp;rlz=1I7DMUS
believe_it
QUOTE
http://www.ghanaweb.com/GhanaHomePage/News...l.php?ID=168077

Feature Article of Saturday, 5 September 2009

Obama Pushes GM Foods on Ghana, Africa

Watch live television from Ghana plus the latest Ghanaian movies plus OBE TV.

I am an African born in America, and I am an admirer and follower of Kwame Nkrumah, Marcus Garvey and Malcolm X. Therefore, this article caused me to have much concern about the direction in which Ghana is moving.

President Obama wishes to introduce the Rockefeller and Gates supported Green Revolution to Africa. He appointed Michael R. Taylor, VP for Public Policy at Monsanto from 1998 to 2001, as Senior Advisor to the Commissioner of the FDA. Taylor, with Rockefeller Foundation funding, authored two papers which tied US agricultural aid to Africa to the implementation of biotechnology, including pesticides and GM seeds.

The "Green Revolution" has led to financial ruin, suicide and cancer for many farmers and farm communities in India, Asia and Latin America. Please see http://www.foodfirst.org/en/node/2515

The Green Revolution has brought about many crop failures in Africa. This includes millions of dollars of lost income suffered by South African farmers when 82,000 hectares of genetically-manipulated corn (maize) failed to produce hardly any seeds. Monsanto offered compensation to those farmers who purchased seeds however, no compensation was offered to farmers who were given seeds. Please see http://www.foodfirst.org/en/node/2504

In the 1990s, USAID, together with Monsanto, helped spearhead a 14-year, $6 million project through the Kenya Agricultural Research Institute (KARI) to develop a genetically modified, virus-resistant sweet potato. The project has proven to be a failure. Local varieties outperformed GM varieties in field trials. Researchers in Uganda developed a virus-resistant hybrid through conventional breeding techniques at a tiny fraction of the cost.

KARI continues to collaborate with the Monsanto Corporation and USAID researching biotechnological projects, advocating a model of agricultural development that relies upon a top-down approach and unproven, expensive investments. Please see http://www.foodfirst.org/en/node/2512

Recently the American Academy of Environmental Medicine called for a moratorium on GMO foods stating that they "pose a serious health risk." These risks include "infertility, immune dysregulation, accelerated aging, dysregulation of genes associated with cholesterol synthesis, insulin regulation, cell signalling, and protein formation, and changes in the liver, kidney, spleen and gastrointestinal system." Please see http://www.aaemonline.org/gmopost.html and http://www.aaemonline.org/gmopressrelease.html

In the 1990's scientists from the US FDA (Food and Drug Administration) warned about the health problems associated with GMO foods. However, high-ranking officials in the FDA quashed these reports. According to documents released from a lawsuit, the scientific consensus from the agency was that GM foods were inherently dangerous, and might create hard-to-detect allergies, poisons, gene transfer to gut bacteria, new diseases and nutritional problems. See http://www.biointegrity.org/list.html

Skipping irrelevant speculation...

President Obama insists that GMO food will be beneficial to Africa. However, he and the First Lady have established an organic garden at the White House and, primarily serve organic food to their children. See http://www.nytimes.com/2009/03/11/dining/11lady.html and http://www.nytimes.com/2009/03/20/dining/20garden.html and http://www.nj.com/parenting/carrie_stetler..._house_mic.html.

The sign of a healthy democracy is an informed populace.

Credit: Kwame Piankhi


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Link from http://www.lavidalocavore.org/diary/2426/a...out-us-food-aid
believe_it
By chance, heard end of Hamburg's speech and Q&A on C-Span. No mention of GMO, a lot of discussion about nutrition labeling - sad, very sad.

QUOTE


Includes:
9:30AM - 11:00AM Concurrent Panel: Are National Safety Standards Public Health Protection or Trade Barriers? How to Address Food Safety Needs in a Global Trading System: A global economy relies on a constant exchange of goods between nations. One unintended consequence is a continuing tension between the goals of maximizing “free trade” and the expectations of American consumers that imported food products will meet the same or higher food safety standards as domestically produced products. roflmbo.gif There is a continuing effort to establish international food safety standards which may not require a level of protection that is at least the same as that in the US. Where some see public health protection, others see “non-tariff trade barriers.” Efforts to assure imported foods are safe may result in other nations restricting imports of US produced products. The panel will discuss these ongoing tensions and offer differing views on whether it is appropriate to balance trade and health and safety considerations and how the balance should be defined and achieved.

11:30AM - 12:45PM Facilitated Discussion: Blogs, Twitter, Websites, Facebook: Everyone Has A Voice, Who Gets Heard?: The public is awash in information, data, opinion, and gossip. New technologies provide endless opportunities for almost everyone to get information and to provide their own views in response. Information from journalists, experts, governments, food companies and consumer organizations is mixed with offerings from those who may have opinions but lack data or expertise. roflmbo.gif A panel will discuss how to turn information about nutrition, food safety and public policy into action and explore the implications of these new technologies for policymaking and science.

Opening day panel,
Facilitated Discussion: Status Report: FDA Modernization Legislation: Congress is poised to substantially reform food safety activities at the Food and Drug Administration. The timing of the 2009 Food Policy Conference provides the opportunity for those attending to hear an up-to-the minute report on the status of the debate over modernizing FDA or, if the legislation has passed, a discussion of the prospects for implementing a newly enacted law.
[color="#FF0000"]Michael R. Taylor
Senior Advisor to the Commissioner
For background, see articles by Jeffrey M Smith or below (first result of Google search of the two names)


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QUOTE
http://www.organicconsumers.org/articles/article_17262.cfm

Unwholesome Regulations on Food
By Latha Jishnu
Business Standard, India, March 14 2009

Straight to the Source: http://www.business-standard.com/india/new...onsfood/351734/

Importing the US system of food regulation to India could prove injurious to health.

New Delhi - For several years now, a beef producer in the US has been trying its best to test its cattle for mad cow disease. The brain-wasting disease is rare, but deadly, since it can kill people who eat infected meat. After the first outbreak of mad cow disease in the US, the beef producer, Creekstone Farms Premium Beef, set up a testing laboratory, the first inside an American meatpacking factory, in 2004 to reassure customers, especially those in overseas markets, that its meat was safe. But guess who has been thwarting the company from taking this basic precaution? None other the US government regulator!

In a strange twist of reasoning, the US Department of Agriculture (USDA) contends that Creekstone Farms, by testing of all its cattle, would raise questions about the safety of other meat. It has, therefore, blocked the sale of testing kits to the company by citing an obscure law.

The USDA’s official position is that allowing the meatpacker to test every cow would undermine its position that random testing is adequate to assure safety. However, many believe that it has buckled to pressure from the big boys of the industry, represented by the National Cattlemen’s Beef Association. Why it should not become the rule is something that the USDA has not explained, more so since the testing would add a mere trifle (10 cents per pound of beef) to the cost. Yet, although some countries have banned American beef, the USDA tests less than 1 per cent of the 100,000 cattle slaughtered daily.

This is not the only case where US food regulations have resulted in a welter of court cases or provoked protests from scientists and consumer groups. There have been sharp criticisms of the functioning regulatory agencies, specially of the US Food and Drug Administration (FDA) which plays a larger role in food safety. Censure of the FDA has become widespread in the wake of the current crisis over salmonella poisoning from contaminated peanuts, but while this relates to shoddy inspection procedures and lax systems, the graver charges against the agency concern regulations which are seen as promoting the interests of large corporations against those of small companies and for ignoring consumer concerns, particularly on biotech products.

Many of these regulations were rushed through by the US government in the 1990s in order to help American companies to commercialise biotechnology before the others. Instead of establishing strict, precautionary regulations that would protect public health and safeguard the environment, the government cobbled together a regulatory system that ironically relied on the companies’ reports of risk assessment and safety tests — a process aided by the revolving door between industry and government.

Employees or consultants for powerful biotech companies were routinely given berths in the regulatory agencies and vice-versa. Take just a couple of examples. Former USDA secretary Ann Veneman served as a director with Calgene before she joined the government, first as the secretary of the California Department of Food and Agriculture. Calgene was the company that pioneered the world’s first genetically modified (GM) food, the Flavr Savr tomato. Another one to make the switch was Linda Fisher, who was head of government affairs at Monsanto before she was appointed deputy administrator of the Environmental Protection Agency, a key regulator in approving GM plants.

The most controversial case, however, is that of Michael R Taylor whose career has swung pendulum-like between Monsanto, for whom he worked as a lawyer for seven years, and the regulatory agencies (the FDA and USDA) during Bill Clinton’s presidency. Taylor, it is widely reported, wrote the FDA’s guidelines on recombinant bovine growth hormone, or rBGH, while serving as its deputy commissioner for policy. The rules virtually ban dairies from making any distinction between products derived from rBGH milk and others. rBGH has become a bitterly contested issue in the US — it is banned in most other countries — because of its links to human cancer and serious health problems in cows.

The hazards are infinitely worse in the case of GM foods, warns Jeffery M Smith, executive director of the Institute for Responsible Technology who was in India recently to caution the country against emulating the US example. “Policymakers assume, wrongly, that the FDA has approved (GM crops)on the basis of extensive tests. The truth is that the regulator has depended entirely on the data provided by the developer company,” says Smith. Worse, most of the research is kept secret under the guise of business confidentiality and very little data is open to public scrutiny.

Unfortunately, the Genetic Engineering Approvals Committee (GEAC), the apex regulator for GM foods in India, has chosen to follow the US precept as it prepares to release its first GM food crop, the Bt brinjal. The GM version of the widely-used brinjal is being promoted by Mahyco, the Indian partner of Monsanto, whose data the GEAC had accepted without question. It was only after a Right To Information petition was filed by an environmental group and a challenge by the company was rejected by the courts that Mahyco agreed to make its safety tests public. Serious questions have now been raised on this data by several leading international scientists whose testimonies have been submitted to the Supreme Court.

Experts are, therefore, advising caution on importing US regulations wholesale. American systems warrant a closer look not merely because the FDA is set to open an open office in this country but because an agricultural partnership launched during the Bush regime is seeking to replicate American policies here through different forums. One such is the Indo-US Knowledge Initiative on Agriculture (KIA), which has just completed its first three-year phase. Kavitha Kuruganti, convener of the Coalition for a GM-Free India, finds that the KIA is focused not so much on technology transfer as on changes in India’s regulatory regime.

Based on a study of the minutes of the six KIA board meetings undertaken while she was at the Secunderabad-based Centre for Sustainable Agriculture, Kuruganti says the forum is recommending changes in Indian regulation, including the critical Seeds Bill, to suit US commercial interests in three important areas: GM organisms, contract farming and intellectual property rights. With US multinationals such as Monsanto and Archer Daniels Midland Co on the KIA board, it is only to be expected that the companies will “drive as many changes as possible to suit their business interests”, she claims.

There is a strong body of opinion which says the KIA should be put under parliamentary scrutiny so that a proper assessment can be made of its contribution to Indian agriculture, specially to the small farmer. But this is an issue that could easily turn into an ideological debate and deflect attention from the key concerns on regulation.

One worrying issue is whether revolving doors are opening up here, too. Making a presentation at a recent Delhi briefing of the International Service for the Acquisition of Agri-biotech Applications (ISAAA) along with its founder Clive James, was C D Mayee, one of India’s top agriculture scientists. Mayee is a director of the ISAAA, which describes itself as a not-for-profit organisation that “delivers the benefits of agricultural biotechnology to resource-poor farmers in developing countries.” However, among the 21 donors to ISAAA are a clutch of biotech seed companies which are seeking to expand their markets. These include Monsanto and Indian companies which come to the GEAC for approvals. Mayee is also co-chair of the regulatory body. Not a few believe there is a patent conflict of interest here.


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believe_it
QUOTE
http://www.nytimes.com/2009/09/10/opinion/...p;th&emc=th

September 10, 2009
NYT Op-Ed Contributor

Big Food vs. Big Insurance

By MICHAEL POLLAN
Berkeley, Calif.


To listen to President Obama’s speech on Wednesday night, or to just about anyone else in the health care debate, you would think that the biggest problem with health care in America is the system itself — perverse incentives, inefficiencies, unnecessary tests and procedures, lack of competition, and greed.

No one disputes that the $2.3 trillion we devote to the health care industry is often spent unwisely, but the fact that the United States spends twice as much per person as most European countries on health care can be substantially explained, as a study released last month says, by our being fatter. Even the most efficient health care system that the administration could hope to devise would still confront a rising tide of chronic disease linked to diet.

That’s why our success in bringing health care costs under control ultimately depends on whether Washington can summon the political will to take on and reform a second, even more powerful industry: the food industry.

According to the Centers for Disease Control and Prevention, three-quarters of health care spending now goes to treat “preventable chronic diseases.” Not all of these diseases are linked to diet — there’s smoking, for instance — but many, if not most, of them are.

We’re spending $147 billion to treat obesity, $116 billion to treat diabetes, and hundreds of billions more to treat cardiovascular disease and the many types of cancer that have been linked to the so-called Western diet. One recent study estimated that 30 percent of the increase in health care spending over the past 20 years could be attributed to the soaring rate of obesity, a condition that now accounts for nearly a tenth of all spending on health care.

The American way of eating has become the elephant in the room in the debate over health care. The president has made a few notable allusions to it, and, by planting her vegetable garden on the South Lawn, Michelle Obama has tried to focus our attention on it. Just last month, Mr. Obama talked about putting a farmers’ market in front of the White House, and building new distribution networks to connect local farmers to public schools so that student lunches might offer more fresh produce and fewer Tater Tots. He’s even floated the idea of taxing soda.

But so far, food system reform has not figured in the national conversation about health care reform. And so the government is poised to go on encouraging America’s fast-food diet with its farm policies even as it takes on added responsibilities for covering the medical costs of that diet. To put it more bluntly, the government is putting itself in the uncomfortable position of subsidizing both the costs of treating Type 2 diabetes and the consumption of high-fructose corn syrup.

Why the disconnect? Probably because reforming the food system is politically even more difficult than reforming the health care system. At least in the health care battle, the administration can count some powerful corporate interests on its side — like the large segment of the Fortune 500 that has concluded the current system is unsustainable.

That is hardly the case when it comes to challenging agribusiness. Cheap food is going to be popular as long as the social and environmental costs of that food are charged to the future. There’s lots of money to be made selling fast food and then treating the diseases that fast food causes. One of the leading products of the American food industry has become patients for the American health care industry.

The market for prescription drugs and medical devices to manage Type 2 diabetes, which the Centers for Disease Control estimates will afflict one in three Americans born after 2000, is one of the brighter spots in the American economy. As things stand, the health care industry finds it more profitable to treat chronic diseases than to prevent them. There’s more money in amputating the limbs of diabetics than in counseling them on diet and exercise.

As for the insurers, you would think preventing chronic diseases would be good business, but, at least under the current rules, it’s much better business simply to keep patients at risk for chronic disease out of your pool of customers, whether through lifetime caps on coverage or rules against pre-existing conditions or by figuring out ways to toss patients overboard when they become ill.

But these rules may well be about to change — and, when it comes to reforming the American diet and food system, that step alone could be a game changer. Even under the weaker versions of health care reform now on offer, health insurers would be required to take everyone at the same rates, provide a standard level of coverage and keep people on their rolls regardless of their health. Terms like “pre-existing conditions” and “underwriting” would vanish from the health insurance rulebook — and, when they do, the relationship between the health insurance industry and the food industry will undergo a sea change.

The moment these new rules take effect, health insurance companies will promptly discover they have a powerful interest in reducing rates of obesity and chronic diseases linked to diet. A patient with Type 2 diabetes incurs additional health care costs of more than $6,600 a year; over a lifetime, that can come to more than $400,000. Insurers will quickly figure out that every case of Type 2 diabetes they can prevent adds $400,000 to their bottom line. Suddenly, every can of soda or Happy Meal or chicken nugget on a school lunch menu will look like a threat to future profits.

When health insurers can no longer evade much of the cost of treating the collateral damage of the American diet, the movement to reform the food system — everything from farm policy to food marketing and school lunches — will acquire a powerful and wealthy ally, something it hasn’t really ever had before.

AGRIBUSINESS dominates the agriculture committees of Congress, and has swatted away most efforts at reform. But what happens when the health insurance industry realizes that our system of farm subsidies makes junk food cheap, and fresh produce dear, and thus contributes to obesity and Type 2 diabetes? It will promptly get involved in the fight over the farm bill — which is to say, the industry will begin buying seats on those agriculture committees and demanding that the next bill be written with the interests of the public health more firmly in mind.

In the same way much of the health insurance industry threw its weight behind the campaign against smoking, we can expect it to support, and perhaps even help pay for, public education efforts like New York City’s bold new ad campaign against drinking soda. At the moment, a federal campaign to discourage the consumption of sweetened soft drinks is a political nonstarter, but few things could do more to slow the rise of Type 2 diabetes among adolescents than to reduce their soda consumption, which represents 15 percent of their caloric intake.

That’s why it’s easy to imagine the industry throwing its weight behind a soda tax. School lunch reform would become its cause, too, and in time the industry would come to see that the development of regional food systems, which make fresh produce more available and reduce dependence on heavily processed food from far away, could help prevent chronic disease and reduce their costs.

Recently a team of designers from M.I.T. and Columbia was asked by the foundation of the insurer UnitedHealthcare to develop an innovative systems approach to tackling childhood obesity in America. Their conclusion surprised the designers as much as their sponsor: they determined that promoting the concept of a “foodshed” — a diversified, regional food economy — could be the key to improving the American diet.

All of which suggests that passing a health care reform bill, no matter how ambitious, is only the first step in solving our health care crisis. To keep from bankrupting ourselves, we will then have to get to work on improving our health — which means going to work on the American way of eating.

But even if we get a health care bill that does little more than require insurers to cover everyone on the same basis, it could put us on that course.

For it will force the industry, and the government, to take a good hard look at the elephant in the room and galvanize a movement to slim it down.

Michael Pollan, a contributing writer for The Times Magazine and a professor of journalism at the University of California, Berkeley, is the author of “In Defense of Food: An Eater’s Manifesto.”


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believe_it
QUOTE
OCA Editors' Note: OCA applauds our ally the Center for Food Safety for this watershed moment in their efforts to bring GMOs under the rule of law. The victory breathes new life into our consumer campaigns for marketplace rejection of food brands that have indicated they would use GMO sugar.

TAKE ACTION: Write to American Crystal Sugar President David Berg who believes consumers acceptance of GMO sugar be "a big nonevent." Tell him you're joining the boycott of foods with GMO sugar.


QUOTE
http://www.organicconsumers.org/articles/article_19177.cfm

Court Rejects Genetically Modified Sugar Beets

By Bob Egelko
The San Francisco Chronicle, September 23, 2009
Straight to the Source


SAN FRANCISCO -- The government illegally approved a genetically modified, herbicide-resistant strain of sugar beets without adequately considering the chance they will contaminate other beet crops, a federal judge in San Francisco has ruled.



Sugar beet at harvest time (Flickr photo by grabe)

The ruling by U.S. District Judge Jeffrey White rejected the U.S. Department of Agriculture's decision in 2005 to allow Monsanto Co. to sell the sugar beets, known as "Roundup-Ready" because they are engineered to coexist with Monsanto's Roundup herbicide.
Sugar beets produce 30 percent of the world's sugar and, according to consumer groups, half the granulated sugar in the United States. This year's planting, centered in Oregon's Willamette Valley, is the first to include a full crop of the Monsanto product.

White said the USDA, in concluding that the new crop would have no significant environmental effects, discounted the likelihood that wind-borne pollen would spread to fields where conventional sugar beets, table beets and the beet variety known as Swiss chard are grown.

Planting genetically modified sugar beets has a "significant effect" on the environment, White said in his ruling Monday, because of "the potential elimination of a farmer's choice to grow non-genetically engineered crops, or a consumer's choice to eat non-genetically engineered food."

He said the department must prepare an environmental impact statement, which would include public input.

White did not immediately prohibit distribution of the genetically modified sugar beets, but a lawyer for plaintiffs in the case said they would ask the judge for an injunction against sales until the review was completed.

The ruling "sends a very clear message to the USDA to protect American farmers and consumers and not the interests of Monsanto," said Kevin Golden, a San Francisco attorney for the nonprofit Center for Food Safety, which opposes genetically modified foods and supports organic farming.

Golden said the ruling could also affect herbicide use, because the Environmental Protection Agency has allowed more herbicide spraying in areas where the resistant crops are grown.

Representatives of the Agriculture Department and Monsanto were unavailable for comment. Luther Markwart, spokesman for the 10,000-member American Sugar Beet Growers Association, said the group is "looking forward to aggressively advocating" for farmers who want to use the altered beets.

The ruling followed a similar decision in 2007 by another federal judge in San Francisco, Charles Breyer, to halt the nationwide planting of Monsanto's genetically engineered strain of alfalfa until the USDA conducted an environmental study. A federal appeals court upheld Breyer's decision last year.

The department's 2005 decision on sugar beets acknowledged that pollen from the genetically modified crop could spread to other beet crops. But the USDA said farmers would not be harmed because they would still be able to buy non-genetically modified seeds.

White, however, cited studies that said winds can carry sugar beet pollen at least 2 1/2 miles, much farther than the voluntary buffer zones between beet crops recommended by Oregon agriculture officials.

He said the department had failed to consider the economic effects of its decision and had provided no evidence for its conclusion that non-genetically modified sugar beets would remain available to farmers.


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believe_it
QUOTE
http://www.nytimes.com/2009/09/23/business/23beet.html

Judge Rejects Approval of Biotech Sugar Beets

September 23, 2009
By ANDREW POLLACK


A federal judge has ruled that the government failed to adequately assess the environmental impacts of genetically engineered sugar beets before approving the crop for cultivation in the United States. The decision could lead to a ban on the planting of the beets, which have been widely adopted by farmers.

In a decision issued Monday, Judge Jeffrey S. White of Federal District Court in San Francisco, said that the Agriculture Department should have done an environmental impact statement. He said it should have assessed the consequences from the likely spread of the genetically engineered trait to other sugar beets or to the related crops of Swiss chard and red table beets.

The decision echoes another ruling two years ago by a different judge in the same court involving genetically engineered alfalfa. In that case, the judge later ruled that farmers could no longer plant the genetically modified alfalfa until the Agriculture Department wrote the environmental impact statement. Two years later, there is still no such assessment and the alfalfa, with rare exceptions, is not being grown.

In the new case, Judge White has not yet decided on the remedy. A meeting to begin that phase of the case is scheduled for Oct. 30.

But the plaintiffs in the lawsuit said they would press to ban planting of the biotech beets, arguing that Judge White’s decision effectively revoked their approval and made them illegal to grow outside of field trials.

“We expect the same result here as we got in alfalfa,” said Andrew Kimbrell, executive director of the Center for Food Safety, a Washington advocacy group that was also involved in the alfalfa lawsuit. “It will halt almost any further planting and sale because it’s no longer an approved crop.”

The Center for Food Safety was joined in the suit by the Sierra Club, the Organic Seed Alliance and High Mowing Organic Seeds, a small seed company. The defendant, the Department of Agriculture, said it was reviewing the decision.

Some beet farmers and sugar processors declined to comment Tuesday on the decision, saying they needed more time to analyze it. But they said that the genetically engineered sugar beets had proved immensely popular since first being widely grown in 2008.

The beets contain a bacterial gene licensed by Monsanto that renders them impervious to glyphosate, an herbicide that Monsanto sells as Roundup. That allows the herbicide to kill weeds without harming the crop.

“Growers have embraced this technology,” said Duane Grant, a farmer in Rupert, Idaho, who said industry surveys suggested that 95 percent of the sugar beets planted this year were genetically modified.

Mr. Grant, who is also the chairman of the Snake River Sugar Company, a grower-owned cooperative, said easier weed control allowed farmers to reduce tillage, which in turn saved fuel and fertilizer and reduced erosion.

Mr. Grant, as well as some other growers, sugar processors and seed companies like Monsanto, had sought to intervene in the case. Judge White said that other than filing a friend-of-the-court brief, they could not participate in the phase of the lawsuit examining whether the Agriculture Department fulfilled its obligations under environmental law.

However, those groups are expected be allowed to take part in the next round of the case, involving the remedies. “We’re going to use that opportunity to advocate the need for that technology and vigorously defend our growers’ freedom to plant Roundup Ready sugar beets,” said Luther Markwart, executive vice president for the American Sugarbeet Growers Association.

Beets supply about half the nation’s sugar, with the rest coming from sugar cane. About 10,000 farmers grow about 1.1 million acres of sugar beets, Mr. Markwart said. That makes it a small crop compared to staples like soybeans and corn.

The Agriculture Department did conduct an environmental assessment before approving the genetically engineered beets in 2005 for widespread planting. But the department concluded there would be no significant impact, so a fuller environmental impact statement was not needed.

But Judge White said that the pollen from the genetically engineered crops might spread to non-engineered beets. He said that the “potential elimination of farmer’s choice to grow non-genetically engineered crops, or a consumer’s choice to eat non-genetically engineered food” constituted a significant effect on the environment that necessitated an environmental impact statement.

In March, Judge White had asked the federal government if the Obama administration would take a different stance in the case than the Bush administration had. The new administration said there would be no change.

David Berg, president of American Crystal Sugar Company, the nation’s largest sugar beet processor, said food companies had accepted sugar from the biotech beets. “They’ve been a big nonevent in terms of customer acceptance,” he said.


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rla
Need for reform in the nation's food supply system is a significant part of the need for reform in the Nation's Health Care system. Together, they make explicit the need for a National Program to promote
person-centered Wellness at the community level...All the evidence supports this general conclussion
so why is there so little push for Wellness and so much resistance to it?
believe_it
I read this great blog every day not because I'm a foodie or gardener but because of excellent objective coverage of GMO news.

QUOTE
http://fanaticcook.blogspot.com/2009/10/ge...isms-whats.html

Genetically Modified Organisms: What's The Problem?

Thursday, October 08, 2009

There's a new interview with Jeffrey Smith, author of Seeds of Deception (which questions the safety of genetically engineered foods) on a site called the Azure Standard. Here are excerpts where Smith answers questions often posed about genetic engineering (GE):


QUOTE
http://www.azurestandard.com/blog/?p=72

An Interview with Jeffrey M. Smith
Oct/Nov 2009
by Susan Booth


Susan Booth: What is the difference between genetic modification versus just regular hybridization or selective breeding?

Jeffrey M. Smith: Genetic engineering is not natural. It carries unique risks and is fraught with unpredicted side effects.

In normal hybridization or selective breeding you take plants from the same species or related species and they essentially have sex and their offspring share genes from both parents. With genetic engineering, you take a single gene or combination of genes from other species, and you manipulate the gene in the laboratory. You add, typically, an "on switch" called a Promoter from a virus and other materials and then you force it into the DNA of the plant. Then you clone the cell into a plant…

The process of insertion, whether through "gene gun" technology or bacterial infection, plus cloning, causes massive collateral damage in the DNA. It leads to hundreds or thousands of mutations up and down the DNA, and hundreds or thousands of genes that can change their levels of expression in the natural plant. These changes can lead to unpredicted side effects, such as new or higher levels of toxins, carcinogens, allergens, or anti-nutrients. And this is not theoretical. They have actually found these types of things in the genetically engineered crops already on the market.

Booth: If it’s that dangerous and has that many problems, why do they do it?

Smith: The White House [George H. W. Bush administration] had been convinced that genetically engineered foods would increase U.S. exports and our domination in world food trade. They ordered the FDA and the other regulatory agencies to fast-track GM foods.

Booth: What are some of the bad things that could happen to children who are consuming a lot of genetically modified foods? I know you talk about allergies and the fact that soy allergies skyrocketed in the U.K. when genetically engineered soy was introduced.

Smith: Well, with allergies, I just found out… Emergency room visits due to allergies doubled in the United States in the five years following the introduction of genetically modified foods.

One top biologist in the world recently told me that he sees the increase in so many health problems in the US in the last 10 or 15 years and he believes that the introduction of genetically engineered foods into the American diet is largely responsible for those changes. So, these could be any of the "new" diseases, or the increases in diseases, from autism and allergies to obesity and diabetes, to digestive system cancers to virtually anything.

Children’s digestive systems, their gut bacteria, their whole defense system is not particularly well-developed, and we find in the only human feeding study ever published, that genes can transfer into the DNA of bacteria living inside our intestines. There’s more opportunity for the DNA to transfer into the gut bacteria [in children because their] DNA is broken down at a slower rate or not at all.

Also, the gut bacteria in the infant, I’m told by doctors, is first populated by the bacteria inside the womb of the mother. So if there are already gut bacteria problems and imbalances due to GMOs in the mother, then that’s also a problem.

If the Bt toxin, which is part of genetically modified corn, causes disturbance in the walls of the intestines, as it may in fact be doing, it might cause some kind of leaky gut which could cause toxicity in the blood. And since the blood-brain barrier in children is not well developed, it could also result in toxicity of the brain, which could contribute to a whole host of some of the psychological disorders and learning disabilities.

I’m mentioning just a small list compared to what could be happening due to GMOs. They’ve found, for example, that both soy and corn have higher levels of lignan, which was not supposed to happen. The metabolic pathway that produces lignan also produces Rotenone, a plant pesticide which is linked to Parkinson’s Disease.
----------

A follow-up to these uncertainties is often, "What is recent research showing?" Unfortunately, there is little research being conducted, as this article from the New York Times explains:
Crop Scientists Say Biotechnology Seed Companies Are Thwarting Research, New York Times, Feb 2009
http://www.nytimes.com/2009/02/20/business...=3&emc=eta1
Biotechnology companies are keeping university scientists from fully researching the effectiveness and environmental impact of the industry’s genetically modified crops, according to an unusual complaint issued by a group of those scientists.

The problem, the scientists say, is that farmers and other buyers of genetically engineered seeds have to sign an agreement meant to ensure that growers honor company patent rights and environmental regulations. But the agreements also prohibit growing the crops for research purposes.

Posted by Bix


.

believe_it
QUOTE(rla @ Sep 24 2009, 10:37 AM) *
Need for reform in the nation's food supply system is a significant part of the need for reform in the Nation's Health Care system. Together, they make explicit the need for a National Program to promote person-centered Wellness at the community level... All the evidence supports this general conclusion so why is there so little push for Wellness and so much resistance to it?


I wonder that myself. Could the lack of push be due to the threat of so-called 'strategic lawsuits against public participation (acronym SLAPP)' triggered by existence of various state Food Disparagement Acts? See post #121 above for full details. That's my leading suspicion for why MSM neglects this entire subject although sheer confusion might be responsible, or insecurity about understanding science, or an averson to being mislabeled a Luddite, etc.

Of course, there is no legitimate excuse for our media's failure to inform the American public about the controversy over biotech foods.

QUOTE(believe_it @ Feb 7 2009, 01:52 AM) *
http://www.alternet.org/story/12910?page=entire

Industry Attacks on Dissent: From Rachel Carson to Oprah
By Laura Orlando
Posted on April 19, 2002


In March 1996, the British government announced that 10 people had died after eating beef from cattle sick with "mad cow disease." A month later, talk-show host Oprah Winfrey discussed the topic on national television.

While interviewing guest Howard Lyman of the Humane Society about his belief that American cattle might be at risk for the disease, Winfrey told her audience, "It has just stopped me cold from eating another burger." A group of Texas cattle ranchers sued Winfrey and Lyman for libeling cattle. Four years and over $1 million later, the two were vindicated in court.

Winfrey and Lyman were sued under the Texas False Disparagement of Perishable Food Products Act. Food disparagement laws are a new tool in an old bag of tricks used by corporations to protect their own economic interests at the expense of public discussion. Silencing public debate with frivolous, time-consuming and costly lawsuits has become so commonplace that the technique has its own name: strategic lawsuits against public participation, or SLAPP suits...

.
believe_it
TV BREAK laugh.gif

Fictionalized treatments (easily ridiculed) of important issues score powerfully with me whenever truth can be discerned at their essence.

In case YOU missed the imperfect* but groundbreaking CSI-Miami - 10/19/09 - Bad Seed, here's a review on-the-day-of-airing by a 'patent lawyer.'
(First they ignore you, then they laugh at you, then they fight you and then you win. - Gandhi)

Broad categories of fist-pumping concepts touched upon in 45 dense minutes of dialogue and imagery include gross bacterial contamination of food; GM/biotech food technology; agribusiness models including cost/benefit analyses; failure of government regulatory agencies to address either food safety issue (sanitation and biotech food) adequately:
    • Seeds can be patented?
    • Food disparagement laws? Say whaaat?
    • Indifference to E. Coli contamination isn't negligent homicide?
    • Independent contractors and subcontractors absolve major food factories of responsibility for gross contamination?
    • Genetic drift (contamination of conventional farm by windblown patented GM seed from adjacent factory farm resulting in lawsuit against hapless farmer and loss of farmland could've been inspired by Vanity Fair article posted upthread)?
    • GM foods contain bacterial, viral components?
    • Revolving door between industry and government regulatory bodies?
    • Risk-benefit analysis (by corporate factory farm agribusiness) includes acceptable morbidity/mortality rates?
*(eg. genetically modified corn tastes like chalk and is not found as corn-on-the-cob. GM corn is used as animal feed and in processed foods as additives such as high fructose corn syrup. An acute illness from GM food is rare; chronic illnesses are another story.) See http://www.seedsofdeception.com/Public/Med...ideos/index.cfm

QUOTE
http://ipbiz.blogspot.com/2009/10/csi-miam...d-portrays.html

IPBiz
Intellectual property news affecting business and everyday life


Monday, October 19, 2009

CSI Miami episode "Bad Seed" portrays an evil patentee


The episode of CSI Miami titled "Bad Seed" (Season 8 Episode 5) has a patent holder on a recombinant corn seed who enforces the patent against a neighboring farmer. Said farmer can't afford a lawyer and has to sell some of his land to settle the patent infringement case. The initial contact of the CSI guy with gun-toting farmer illustrates how the farmer feels about this patent infringement.

HOWEVER, it seems that this recombinant corn has some side effects (as to botulism), and the CSI team goes to the farmer to get some evidence, allowing the farmer to get even, at least as to shafting the bio company.

The recombinant plot line is not unrelated to an episode of "Eleventh Hour" broadcast last year. See "Eleventh Hour" depicts evil university/industry cabal in biotech: http://ipbiz.blogspot.com/2008/12/eleventh...picts-evil.html

However, "Bad Seed" includes a case of E. Coli poisoning, and has a bit of a twist in deep-sixing this part of the case because
#1. of laws against disparagement of food
#2. of a flagrant conflict-of-interest, wherein the government official who would investigate is an ex-VP of the guilty food/bio company

One notes that the bio company skates on all criminal charges.

However, the lawyer for the bio company, a Harvard law School graduate, allows the bio CEO to talk directly to Horatio, therein commenting about how 500 people eating has more value than one death. H. dutifully records the conversation, to be used in a later civil suit.

As to portrayals, the patentee comes off as a villainous predator, not unlike depictions in patent reform. The Harvard lawyer comes off as an arrogant fool, allowing his company to be laid low by his own hubris. And John Q. Public is not protected against either E. Coli in salad or against Frankenfood corn.

Well, Halloween and patent reform are coming.

About Me
I'm a patent lawyer located in central New Jersey. I have a J.D. from the University of Chicago and a Ph.D. from Stanford University, where I studied graphite intercalation compounds at the Center for Materials Research. I worked at Exxon Corporate Research in areas ranging from engine deposits through coal and petroleum to fullerenes. An article that I wrote in The Trademark Reporter, 1994, 84, 379-407 on color trademarks was cited by Supreme Court in Qualitex v. Jacobson, 514 US 159 (1995) and the methodology was adopted in the Capri case in N.D. Ill. An article that I wrote on DNA profiling was cited by the Colorado Supreme Court (Shreck case) and a Florida appellate court (Brim case). I was interviewed by NHK-TV about the Jan-Hendrik Schon affair. I am developing ipABC, an entity that combines rigorous IP analytics with study of business models, to optimize utilization of intellectual property. I can be reached at C8AsF5 at yahoo.com.


QUOTE
http://www.bscreview.com/2009/10/csi-miami-bad-seed-review/

After a fight between Horatio and the huge agriculture corporation’s CEO (H lost. Ouch!), it’s back to teamwork, the underlying theme of the show. Over and over again, we see the team working together on one case with no sub-plot. It was a nice change. We also are treated to a mini-treatise on modern agriculture courtesy of Warren and, later, the CEO, played by Stephen Culp. Mr. Culp must get a lot of casting calls to play a-hole hotshots, because he brings his A Game to this episode. The little snide chuckle as he leaves the station the first time is nicely swallowed at the end, when Horatio pulls out the tape recorder, revealing their entire conversation about “acceptable losses of human life” is okay if it feeds hundreds. Culp’s CEO makes the case for modern agriculture: food prices would skyrocket, people would starve, and the most fundamental of all, people don’t care where their food comes from. All valid points, to be sure, but he’s still an arrogant ass about it. Legal scholars out there: is what Horatio did legal? Seems shady, but it still makes you pump your fist in victory.
COMMENTS:
cody says:
October 20, 2009 at 10:35 am
I am big fan of the show but last night episode they totaly bashed on agriculture a subject the writers clearly know nothing about. 98 % of all farms in the US are owned by individuals or family corparations. The use of GM crops in the US is highly regulated and that so called gm corn would have never been approved. All corn is gentically modifed. There is no evidence to support that eating organic products are actually healthier for you. Feedlot operations are regulated by the USDA and EPA and must have approved waste water systems. Cattle are able to digest corn they have a four chambered stomach designed to digest the protien in corn. For more info check out the facts for yourself dont let some TV writer tell you that your food is unsafe when the have probably have never been to a farm or been invovled with production agriculture.

Matt says:
October 20, 2009 at 4:14 pm
As a an active member of the biotech community, i can’t say how angry this episode has made me and so many other fellow coworkers. You’ve lost several viewers. Where were your technical consultants on the plausibility of something like this happening in a mass produced transgenic crop. I would also like to point out that i’m some ‘heartless corporate shill’, but that i in fact work for a regulatory agency.

Zzzzt. says:
October 20, 2009 at 4:20 pm
Wow, cody… talk about propaganda – sounds like you’ve been fed bad infomarion all along. Proof? Define ‘ruminant’ for me…more? If USDA/EPA/FDA regulation equals safety, why do so many die (yes, die) each year from food borne illness (e.coli, etc)…and where did you get your 98% from? Check your facts again and find out how many ‘family corporations’ are subsidaries of majors. Not all corn is GMO, but most is – and that is both scary and sad – nearly everything in the episode was spot on truth…and yes, I do run a farm..
believe_it
QUOTE
http://thinkbeforeyoupink.org/?page_id=2


VIDEO


Eli Lilly is now the sole manufacturer of rBGH — the artificial growth hormone given to dairy cows that increases people's risk of cancer. Eli Lilly also manufactures breast cancer treatment medications and a pill that “reduces the risk” of breast cancer. Eli Lilly is milking cancer. Tell them to stop making rBGH.
.


QUOTE
http://www.organicconsumers.org/articles/article_19530.cfm

ACTON ALERT

Tell the rBGH Profiteers Why You Buy Organic to Avoid Genetically Modified Bovine Growth Hormone

Following up on our successful campaign against Yoplait and Dannon, the Organic Consumers Association is now asking our members to write to ice cream companies that still allow the use of genetically modified bovine growth hormone (Dreyer's, Edy's, Nestle, Haagen-Dazs, Klondike, Good Humor, Breyer's). Your letter will also go to the manufacturer and distributor of rBGH, Elanco and Eli Lilly, which recently purchased the product from Monsanto, and the National Federation of Milk Producers which allows rBGH in its new Dairy FARM (Farmers Assuring Responsible Management) program.


.
believe_it
QUOTE
http://www.huffingtonpost.com/jeffrey-smit...c_b_312754.html

[color="#000000"]Is Eli Lilly Milking Cancer by Promoting and Treating It?

by Jeffrey M Smith
Octobert 07, 2009


Breast Cancer Action and a coalition of consumer and health organizations have launched a campaign called Milking Cancer, where you can demand from Eli Lilly that they withdraw their dangerous bovine growth hormone from the market. For more on bovine growth hormone, see the 18-minute film, Your Milk on Drugs.

Years ago, an owner of a glass company was arrested for throwing bricks through store windows in his town. What a way to increase business! Has Eli Lilly figured out the drug equivalent of breaking, then fixing our windows?

In August 2008, the huge drug company agreed to buy Monsanto's bovine growth hormone (rbST or rbGH), which is injected into cows in the US to increase milk supply. It was an odd choice at the time. A reporter asked Lilly's representative why on earth his veterinary division Elanco just paid $300 million for a drug that other companies wouldn't touch with a ten foot pole. The drug's days were obviously numbered. The former head of the American Medical Association has urged hospitals to stop using dairy products from rbGH-injected cows, the American Nurses Association came out against it, even Wal-Mart has joined the ranks of numerous retailers and dairies loudly proclaiming their cows are rbGH-free. In fact, Monsanto's stock rose by almost 5% when the sale was announced, and Eli Lilly's dropped by nearly 1%.

The main reason for the unpopularity of this hormone, which is banned in most other industrialized countries, is the danger of insulin-like growth factor 1 (IGF-1). Dozens of studies confirm that IGF-1, which accelerates cell division, substantially increases the risk of breast, prostate, colon, lung, and other cancers. Normal milk contains IGF-1, milk drinkers have higher levels of IGF-1, and the milk from cows injected with Eli Lilly's drug has much greater amounts of IGF-1. You can connect the dots.

Would it be too crass to point out the obvious conflict-of-the-public's-interest that Eli Lilly also markets cancer drugs? In fact their drug Evista, which might help reduce the risk of breast cancer, may lower IGF-1 (according to one small study). So on the one hand, Eli Lilly pushes a milk drug that might increase cancer, and on the other, it comes to the rescue with drugs to treat or "prevent" cancer. Call it the perfect cancer profit cycle.

It gets better.

Cows treated with rbGH have much higher incidence of mastitis, a painful infection of the udder. This results in more pus in the milk (yuck). But don't worry. It's Eli Lilly to the rescue again. They are one of the companies happy to sell antibiotics to dairy farmers to treat the infection--which can't help but increase antibiotic resistance in humans (double yuck).

History of Lawsuits and Criminal Charges

But would Eli Lilly consciously risk our health just to increase their profit? What kind of company are they and can we trust them with our food? If recent events are any indication, you better look for rbGH-free labels.

A December 17, 2006 New York Times article revealed that according to hundreds of internal documents and emails,
Eli Lilly has engaged in a decade-long effort to play down the health risks of Zyprexa. ... Lilly executives kept important information from doctors about Zyprexa's links to obesity and its tendency to raise blood sugar -- both known risk factors for diabetes. ... Lilly was concerned that Zyprexa's sales would be hurt if the company was more forthright about the fact that the drug might cause unmanageable weight gain or diabetes.

Their own surveys revealed that 70% of psychiatrists had at least one patient "develop high blood sugar or diabetes while taking Zyprexa." And 30% of patients taking the drug for a year gained at least 22 pounds--some over 100 pounds. But Lilly told their sales team, "Don't introduce the issue!!!"

One doctor even warned: "Unless we come clean on this, it could get much more serious than we might anticipate." It did indeed get serious. They paid out hundreds of millions in settlements to people who claimed they developed diabetes or other disorders.

But Lilly's Zyprexa troubles were not over. In early 2009, they were forced to pay a record-setting $1.42 billion settlement with the Justice Department, and another record-setting state consumer protection claim of $62 million, for illegally marketing the drug to children and the elderly. It emerged in June of this year that Lilly "officials wrote medical journal studies about the antipsychotic Zyprexa and then asked doctors to put their names on the articles, a practice called 'ghostwriting.'"

Eli Lilly was also the maker of the infamous Diethylstilbestrol (DES), a synthetic estrogen. Starting in 1938, it was prescribed to pregnant women to prevent miscarriages and other problems. Although in 1953, research showed that it didn't actually prevent miscarriages, it continued to be used until 1971, when the FDA alerted the public that the daughters exposed to DES in the womb were at risk of a rare vaginal cancer. An estimated 5-10 million pregnant women received DES. The civil courts held Lilly liable because they should have foreseen (based on prior information) that DES might cause cancer and that Lilly should have done the proper testing before marketing it.

Rigging Research

In the late 1980s Eli Lilly was one of four companies (including American Cyanamid, Upjohn, and Monsanto) that tried to get their version of bovine growth hormone approved by the FDA. I sat down with Dr. Richard Burroughs, who was a lead reviewer for the agency on these applications. He didn't have kind words to say about the companies. "They didn't follow good science and they didn't follow regulations for adequate well controlled studies," he said. "They just went out and skewed the data."

He said, for example, that Eli Lilly had mysteriously lost organ samples that may have shown problems in injected cows. And their researchers came up with creative ways to hide reproductive changes in the animals. Specifically, injections appeared to suppress cows' regular menstrual cycle or reduce the visual symptoms. The company was required to report the number of cows "in heat," but was told by the FDA that they could not use bulls to identify them. If bulls were needed, then the label on their drug would have to inform farmers that they would need a bull to help identify which cows were in heat. And most farms didn't have bulls.

According to Burroughs, FDA investigators figured out that Lilly researchers secretly pumped up a heifer--a young female cow--with male hormones, so that the transgendered animal would act like a male and be attracted to the cows in heat. Lilly followed the letter of the law by not using a bull, but well, you can decide if you want to trust these guys.

Eventually, Lilly and two other companies withdrew their products, leaving Monsanto's brand of rbGH as the only one that got approved and marketed. But Lilly worked a deal where they represented Monsanto's drug outside the US. They sell it in 20 countries, including South Africa, Brazil, Colombia, Honduras, Kenya and Mexico. And now, they offer it in the US as well.

Human Reproductive Problems from Drugged Milk

In May 2006, an article in the Journal of Reproductive Medicine concluded that rbGH use, and the subsequent increase in IGF-1 in the US diet, is probably the reason why we have much higher levels of fraternal twins compared to the UK, where rbGH is banned.

Mothers with twin births are more likely to suffer from hypertension, gestational diabetes, hemorrhage, and miscarriage. Twin babies are more likely to be born prematurely and suffer from birth defects, mental retardation, cerebral palsy, vision and hearing disorders, and serious organ problems. How many drugs do you suppose Eli Lilly sells to treat these disorders?

Tell Eli Lilly to take rbGH off the market and out of your milk. To find non-rbGH dairy products, check out the non-GMO shopping section at http://www.responsibletechnology.org/GMFree/Home/index.cfm

.
believe_it
QUOTE
http://www.huffingtonpost.com/jeffrey-smit...c_b_312754.html

Is Eli Lilly Milking Cancer by Promoting and Treating It?

by Jeffrey M Smith
Octobert 07, 2009


Breast Cancer Action and a coalition of consumer and health organizations have launched a campaign called Milking Cancer, where you can demand from Eli Lilly that they withdraw their dangerous bovine growth hormone from the market. For more on bovine growth hormone, see the 18-minute film, Your Milk on Drugs.

Years ago, an owner of a glass company was arrested for throwing bricks through store windows in his town. What a way to increase business! Has Eli Lilly figured out the drug equivalent of breaking, then fixing our windows?

In August 2008, the huge drug company agreed to buy Monsanto's bovine growth hormone (rbST or rbGH), which is injected into cows in the US to increase milk supply. It was an odd choice at the time. A reporter asked Lilly's representative why on earth his veterinary division Elanco just paid $300 million for a drug that other companies wouldn't touch with a ten foot pole. The drug's days were obviously numbered. The former head of the American Medical Association has urged hospitals to stop using dairy products from rbGH-injected cows, the American Nurses Association came out against it, even Wal-Mart has joined the ranks of numerous retailers and dairies loudly proclaiming their cows are rbGH-free. In fact, Monsanto's stock rose by almost 5% when the sale was announced, and Eli Lilly's dropped by nearly 1%.

The main reason for the unpopularity of this hormone, which is banned in most other industrialized countries, is the danger of insulin-like growth factor 1 (IGF-1). Dozens of studies confirm that IGF-1, which accelerates cell division, substantially increases the risk of breast, prostate, colon, lung, and other cancers. Normal milk contains IGF-1, milk drinkers have higher levels of IGF-1, and the milk from cows injected with Eli Lilly's drug has much greater amounts of IGF-1. You can connect the dots.

Would it be too crass to point out the obvious conflict-of-the-public's-interest that Eli Lilly also markets cancer drugs? In fact their drug Evista, which might help reduce the risk of breast cancer, may lower IGF-1 (according to one small study). So on the one hand, Eli Lilly pushes a milk drug that might increase cancer, and on the other, it comes to the rescue with drugs to treat or "prevent" cancer. Call it the perfect cancer profit cycle.

It gets better.

Cows treated with rbGH have much higher incidence of mastitis, a painful infection of the udder. This results in more pus in the milk (yuck). But don't worry. It's Eli Lilly to the rescue again. They are one of the companies happy to sell antibiotics to dairy farmers to treat the infection--which can't help but increase antibiotic resistance in humans (double yuck).

History of Lawsuits and Criminal Charges

But would Eli Lilly consciously risk our health just to increase their profit? What kind of company are they and can we trust them with our food? If recent events are any indication, you better look for rbGH-free labels.

A December 17, 2006 New York Times article revealed that according to hundreds of internal documents and emails,
Eli Lilly has engaged in a decade-long effort to play down the health risks of Zyprexa. ... Lilly executives kept important information from doctors about Zyprexa's links to obesity and its tendency to raise blood sugar -- both known risk factors for diabetes. ... Lilly was concerned that Zyprexa's sales would be hurt if the company was more forthright about the fact that the drug might cause unmanageable weight gain or diabetes.
Their own surveys revealed that 70% of psychiatrists had at least one patient "develop high blood sugar or diabetes while taking Zyprexa." And 30% of patients taking the drug for a year gained at least 22 pounds--some over 100 pounds. But Lilly told their sales team, "Don't introduce the issue!!!"

One doctor even warned: "Unless we come clean on this, it could get much more serious than we might anticipate." It did indeed get serious. They paid out hundreds of millions in settlements to people who claimed they developed diabetes or other disorders.

But Lilly's Zyprexa troubles were not over. In early 2009, they were forced to pay a record-setting $1.42 billion settlement with the Justice Department, and another record-setting state consumer protection claim of $62 million, for illegally marketing the drug to children and the elderly. It emerged in June of this year that Lilly "officials wrote medical journal studies about the antipsychotic Zyprexa and then asked doctors to put their names on the articles, a practice called 'ghostwriting.'"

Eli Lilly was also the maker of the infamous Diethylstilbestrol (DES), a synthetic estrogen. Starting in 1938, it was prescribed to pregnant women to prevent miscarriages and other problems. Although in 1953, research showed that it didn't actually prevent miscarriages, it continued to be used until 1971, when the FDA alerted the public that the daughters exposed to DES in the womb were at risk of a rare vaginal cancer. An estimated 5-10 million pregnant women received DES. The civil courts held Lilly liable because they should have foreseen (based on prior information) that DES might cause cancer and that Lilly should have done the proper testing before marketing it.

Rigging Research

In the late 1980s Eli Lilly was one of four companies (including American Cyanamid, Upjohn, and Monsanto) that tried to get their version of bovine growth hormone approved by the FDA. I sat down with Dr. Richard Burroughs, who was a lead reviewer for the agency on these applications. He didn't have kind words to say about the companies. "They didn't follow good science and they didn't follow regulations for adequate well controlled studies," he said. "They just went out and skewed the data."

He said, for example, that Eli Lilly had mysteriously lost organ samples that may have shown problems in injected cows. And their researchers came up with creative ways to hide reproductive changes in the animals. Specifically, injections appeared to suppress cows' regular menstrual cycle or reduce the visual symptoms. The company was required to report the number of cows "in heat," but was told by the FDA that they could not use bulls to identify them. If bulls were needed, then the label on their drug would have to inform farmers that they would need a bull to help identify which cows were in heat. And most farms didn't have bulls.

According to Burroughs, FDA investigators figured out that Lilly researchers secretly pumped up a heifer--a young female cow--with male hormones, so that the transgendered animal would act like a male and be attracted to the cows in heat. Lilly followed the letter of the law by not using a bull, but well, you can decide if you want to trust these guys.

Eventually, Lilly and two other companies withdrew their products, leaving Monsanto's brand of rbGH as the only one that got approved and marketed. But Lilly worked a deal where they represented Monsanto's drug outside the US. They sell it in 20 countries, including South Africa, Brazil, Colombia, Honduras, Kenya and Mexico. And now, they offer it in the US as well.

Human Reproductive Problems from Drugged Milk

In May 2006, an article in the Journal of Reproductive Medicine concluded that rbGH use, and the subsequent increase in IGF-1 in the US diet, is probably the reason why we have much higher levels of fraternal twins compared to the UK, where rbGH is banned.

Mothers with twin births are more likely to suffer from hypertension, gestational diabetes, hemorrhage, and miscarriage. Twin babies are more likely to be born prematurely and suffer from birth defects, mental retardation, cerebral palsy, vision and hearing disorders, and serious organ problems. How many drugs do you suppose Eli Lilly sells to treat these disorders?

Tell Eli Lilly to take rbGH off the market and out of your milk. To find non-rbGH dairy products, check out the non-GMO shopping section at
http://www.responsibletechnology.org/GMFree/Home/index.cfm

.

believe_it
QUOTE
http://www.democracynow.org/2009/11/17/oba...executive_to_be

Obama Nominates Pesticide Executive to Be Chief Agricultural Negotiator in the Office of the US Trade Representative

November 17, 2009

VIDEO

President Obama’s nominee for the Chief Agricultural Negotiator in the office of the US Trade Representative, Islam Siddiqui is currently a vice president at CropLife America, a coalition of the major industrial players in the pesticide industry, including Syngenta, Monsanto, and Dow Chemical. He was previously a lobbyist for CropLife and also served in the US Department of Agriculture under President Clinton and the California Department of Food and Agriculture. A coalition of over eighty environmental, family farm and consumer advocacy organizations have sent a letter to the Senate Finance Committee urging them to reject his nomination. [includes rush transcript]

GUEST:
Marcia Ishii-Eiteman, senior scientist at the Pesticide Action Network of North America and one of those leading the charge against Siddiqui’s nomination.

TRANSCRIPT:
AMY GOODMAN: At the end of the broadcast, we’ll look at poverty in the world and the UN food summit, but right now we look at President Obama’s nominee for the Chief Agricultural Negotiator in the office of the US Trade Representative. Islam Siddiqui is currently vice president at CropLife America, a coalition of the major industrial players in the pesticide industry, including Syngenta, Monsanto, Dow Chemical. He was previously a lobbyist for CropLife and also served in the US Department of Agriculture under President Clinton and the California Department of Food and Agriculture.

Over forty-six agribusiness groups signed a letter supporting his nomination, but a coalition of over eighty environmental, family farm and consumer groups sent a letter to the Senate Finance Committee urging them to reject his nomination. The letter says Siddiqui’s record and statements, quote, "show his clear bias in favor of chemical-intensive and unproven biotechnology practices that imperil both our planet and human health while undermining food security and exacerbating climate change,” unquote. Siddiqui defended his record at a Senate committee hearing earlier this month, and a final vote is expected before the World Trade Organization ministerial conference November 30th.

Marcia Ishii-Eiteman is a senior scientist at the Pesticide Action Network of North America and one of those leading the charge against Siddiqui’s nomination, joining us here in San Francisco.

Welcome to Democracy Now! What are your concerns with his nomination?

MARCIA ISHII-EITEMAN: Thank you, Amy. Well, it’s very good to be here.

Our concerns are quite simple. Putting a pesticide pusher in charge of US agriculture, particularly in the Trade office, is bad government. It’s not what Obama promised us during his campaign trail. He did say no lobbyists in the White House. And we know that Islam Siddiqui is a former paid lobbyist for CropLife and is currently and has been for the last many years a senior executive at this association.

AMY GOODMAN: Explain what CropLife is.

MARCIA ISHII-EITEMAN: CropLife is the pesticide industry’s trade association. They’re the major lobbying group. And as you mentioned earlier, their members consist of Monsanto, Dow, DuPont, all the major pesticide and biotech manufacturers. What their agenda is is actually quite straightforward. It’s opening new markets for pesticides and for the genetically engineered seeds that go with them. Their agenda is also to weaken international environmental treaties and any kind of environmental protections or regulations that might somehow get in the way or constrain the production, sale and export of their products.

AMY GOODMAN: Talk about the organizing that’s going on right now and if you see Siddiqui’s nomination as indicative of the whole approach of the Obama administration. I mean, you have Michelle Obama, the main advocate now for organic farming, or at least organic gardening at the White House.

MARCIA ISHII-EITEMAN: Correct, and it’s rather ironic in that this appointment of a CropLife representative, Mr. Siddiqui, he comes from the very same organization that infamously shuddered at Michelle Obama’s planting of this White House organic garden.

AMY GOODMAN: Explain.

MARCIA ISHII-EITEMAN: Well, when she first announced and began developing this organic garden at the White House as a way of highlighting to the public and letting people know that local fresh and organic produce is actually healthier for our bodies and for our children, CropLife’s regional partner in the Midwest sent a letter to Michelle Obama expressing their deep concern that she was setting a bad example for the rest of the country by not using their chemical pesticides. And then they organized a letter writing campaign to urge her to abandon this practice and start using pesticides as soon as possible.

So there’s a great deal of irony here, but the problem is—goes deeper than the irony, and it even goes deeper than this revolving door that we’re seeing. I think what we have with the Obama administration is a very mixed bag of let’s try to do both and everything together, but predominantly, at the basis of the administration’s agriculture policy is a commitment to a fundamentally flawed industrial model of agriculture that is chemically intensive, energy and water intensive, and that is not the solution for the kinds of changes that the planet and US farmers, in particular, are facing in the coming years and decades with climate change, water scarcity and this rapidly diminishing supply of fossil fuels. What we really need to be doing is getting off the pesticide GMO treadmill and moving as quickly as possible on to the right kind of agroecologically based farming that history and science now tells us is really the most robust way forward.

AMY GOODMAN: How do you think his nomination squares with the nomination of Kathleen Merrigan, an advocate of sustainable agriculture, as Deputy Agriculture Secretary?

MARCIA ISHII-EITEMAN: That, there’s a quite a contradiction here. You know, we get, on the one hand, Tom Vilsack as head of USDA, very fine personal qualities, but a very strong commitment, again, to genetically modified organisms and biotech as the latest shiny new technology that we can put on the rest of the world. Then we have Kathleen Merrigan, yes, who is well known for her interest and support of organic farming. So what we have is this very inconsistent policy. But underneath—and perhaps what’s most important is where the key people in the administration and in US agriculture are going. And so, putting Siddiqui in charge of the US Trade Office is very telling.

It’s a bankrupt policy for this country and for the rest of the world. It may seem that, oh, it’s right, what we need is to have agricultural exports increasing and to get our GMOs onto the market, but we’re really behind the times. The rest of the world does not want our GMOs. They have made that clear. Trying to push them forward, in the face of history, in the face of science, is not the best solution. The most comprehensive assessment of agriculture today, the UN-led International Assessment of Agricultural Knowledge, Science and Technology for Development, or the IAASTD report, has said very clearly that business as usual is not an option. We must shift away from these uniform, single, high-tech, and frankly corporate control solutions, like chemical pesticides and biotech, towards agroecological, resilient and regenerative farming systems. But these kinds of changes are really anathema to CropLife and to the kinds of crop protection products that Mr. Siddiqui has been promoting throughout most of his career.

AMY GOODMAN: Well, speaking of the United Nations, we’re going to turn now to the United Nations food summit that’s taking place in Rome. Marcia Ishii-Eiteman, I want to thank you very much for being with us, senior scientist at the Pesticide Action Network. We will link to their letter to the Senate committee on our website at
http://www.democracynow.org/

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QUOTE
http://www.panna.org/files/FINAL-Finance%2...er-Siddiqui.pdf

Re: Nomination of Islam Siddiqui as Chief Agriculture Negotiator for the United States Trade Representative

Dear Chairman Baucus and Ranking Member Grassley:

The following organizations representing environmental, consumer, anti-hunger, family farm, farmworker, fishing groups, sustainable agriculture and other advocacy groups are writing to express our opposition to the nomination of Islam Siddiqui as Chief Agriculture Negotiator at the office of the United States Trade Representative. We urge the Senate Finance Committee to reject Siddiqui’s appointment.

Siddiqui’s record at the U.S. Department of Agriculture and his role as a former registered lobbyist for CropLife America (whose members include Monsanto, Syngenta, DuPont and Dow), reveals him to be consistently in favor of agribusinesses’ interests over the interests of consumers, the environment and public health. His appointment sends an unfortunate signal to the rest of the world that the United States plans to continue down the failed path of industrial
agriculture by promoting toxic pesticides, inappropriate biotechnologies and unfair trade agreements on nations that do not want and can least afford them.
As the global food crisis deepens and negotiators prepare to meet at the upcoming World Trade Organization ministerial on November 30, the United States needs a trade negotiator who understands that current trade agreements work neither for farmers nor the world’s hungry.

Siddiqui’s record and statements in his government positions and at CropLife America show his clear bias in favor of chemical-intensive and unproven biotechnology practices that imperil both our planet and human health while undermining food security and exacerbating climate change. We believe Siddiqui’s nomination has severely weakened the Obama Administration’s credibility in promoting healthier and more sustainable local food systems here at home. Siddiqui’s confirmation would send a message to the world that the United States continues to place the vested interests of our chemical pesticide and biotech industries ahead of concern for public health, the environment, and the well-being of farmworkers and communities around the world.

With farmers here and abroad struggling to respond to water scarcity and increasingly volatile growing conditions, we need a resilient and restorative model of agriculture that adapts to and mitigates these effects of climate change. In the most comprehensive analysis of global agriculture to date, the International Assessment of Agricultural Knowledge, Science and Technology for Development (IAASTD) states unequivocally that “business as usual is not an option.” We need a new, sustainable model of agriculture that regenerates soil health, sequesters carbon, feeds communities, protects farmworkers and puts profits back in the hands of farmers and rural communities. Siddiqui’s clear track record favors none of these solutions.

We call on the Senate Finance Committee to reject Islam Siddiqui’s nomination and reorient trade policy to serve the interests of family farmers, farmworkers, consumers and the planet.

Sincerely,

Alaska Community Action on Toxics
AllergyKids
American Raw Milk Producers Pricing
Association
Beyond Pesticides
Breast Cancer Action
California Food and Justice Coalition
Californians for GE-Free Agriculture
Californians for Pesticide Reform
California Rural Legal Assistance Foundation
Center for Environmental Health (CA)
Center for Food Safety
Center on Race, Poverty & the Environment
Central Florida Jobs with Justice
Columban Center for Advocacy and Outreach
Community Farm Alliance (KY)
Concerned Citizens for Clean Air (OR)
Cornucopia Institute
EarthJustice
Equal Exchange
Family Farm Defenders
Farm and Ranch Freedom Alliance
Farm Worker Pesticide Project (WA)
Farmworker Association of Florida
Farmworker Justice
Farmworker Self-Help (FL)
Food & Water Watch
Food First/Institute for Food and Development Policy
Food for Maine’s Future
Florida Immigrant Coalition
Food Democracy Now!
Florida Organic Growers
Fresno Metro Ministry
Friends of the Earth
Greenpeace US
Grassroots International
Indiana Toxics Action
Innovative Farmers of Ohio
Institute for Agriculture & Trade Policy
Iowa Citizens for Community Improvement
Kids for Saving Earth
Kentucky Environmental Foundation
Land Stewardship Project
Maine Fair Trade Campaign
Maine Organic Farmers and Gardeners Association
Maryland Pesticide Network
Mississippi Association of Cooperatives
Missouri Rural Crisis Center
Mvskoke Food Sovereignty Initiative (OK)
National Family Farm Coalition
National Farm Worker Ministry
National Latino Farmers & Ranchers Trade Association
New York Environmental Law & Justice Project
Northeast Organic Farming Association
Interstate Council (NOFA-IC)
Northern Plains Resource Council (MT)
Northwest Atlantic Marine Alliance
Oakland Institute
Ohio Conference on Fair Trade
Oklahoma Black Historical Research Project
Oregon Fair Trade Campaign
Oregon Toxics Alliance
Organic Consumers Association
Partners for the Land & Agricultural
Needs of Traditional Peoples (WV)
Pesticide Action Network North America
Pesticide Free Zone
Pesticide Watch
Public Citizen
Rural Advancement Foundation International – USA
Rural Advancement Fund
Rural Coalition
Safe Alternatives for our Forest Environment (CA)
Science and Environmental Health Network
Sciencecorps
Search for the Cause (CA)
Sierra Club
Small Holders Alliance of Massachusetts
Washington Fair Trade Coalition
Western Organization of Resource Councils
World Hunger Year

Cc: Members of the Senate Finance Committee


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believe_it
Link from http://www.organicconsumers.org/ as, helpfully, are most links within the article, providing important backstory and context.

ESSENTIAL READING
QUOTE
http://capwiz.com/grassrootsnetroots/issue...lertid=14359511

Take Action: Stop Shah, Another of Obama's Biotech Boosters

Rajiv Shah, currently the USDA Under Secretary for Research, Education and Economics and Chief Scientist, has been nominated by President Obama to lead USAID.

Shah is on the board of directors for the Alliance for a Green Revolution in Africa (AGRA) and was the director of the Gates Foundation's Agriculture Development program. AGRA and the Gates Foundation have been criticized for working closely with Monsanto and its non-profit research arm, the Danforth Center. Links and collaborations include project partnerships, hiring one another's employees and making donations to one another's projects. At the Gates Foundation, Shah supervised Lawrence Kent, who had been the director of international programs at the Danforth Center and Monsanto vice president Robert Horsch, a scientist who led genetic engineering of plants at the seed giant.

In his short tenure at the USDA, he has used connections made at the Gates Foundation, which has distributed $37 million in grants for genetic engineering, to fill the USDA's Research, Education and Economics mission area with biotech scientists and advocates. These include Roger Beachy who directed Monsanto's Danforth Center, Maura O'Neill who ran a public-private venture dedicated to drawing biotech companies to the Seattle area where the Gates Foundation is based, and Rachel Goldfarb, another former Gates employee.

Shah has used his USDA post to champion genetic engineering and other novel technologies. In a report to Congress earlier this year on programs delivered by his mission area, Shah emphasized technology over ecology, saying, "We can build on tremendous recent scientific discoveries - incredible advances in sequencing plant and animal genomes, and the beginnings of being able to understand what those sequences actually mean. We have new and powerful tools in biotechnology and nanotechnology."

He has also directed millions of dollars toward GMO research. Shah has already awarded approximately $64 million in grants to improve crop characteristics through plant breeding, genetics and genomics.

These include $46 million through the Specialty Crop Research Initiative. (This money may not go exclusively to GMO research projects, but "science-based tools," "genetics and genomics," and "innovations and technologies," describe the initiative, while there is no mention of organic practices, conventional breeding or integrated pest management.)

Another $7 million goes to several universities for research to develop stress-resistant crops, a research topic that Monsanto promotes as their raison d'etre, despite the fact that they have never commericialized a single stress-resistant GMO plant, while hundreds of thousands of stress-resistant varieties are utilized by traditional farmers around the world who have saved seed and bred their plants conventionally for centuries.

The GMO research grants also include $11 million in Coordinated Agricultural Project grants to four research universities to study “plant genomics and ways to improve the nutrition and health values of important crops.” Expect more GMO tomatoes, potatoes, barley, soybean, and trees. And be on the lookout for new, GMO legumes embedded with cholesterol and diabetes drugs.

According to a USDA press release on the awards, “Because humans consume more legumes than any other crop, this research has the potential to reduce cholesterol and sugar levels, which in turn can prevent or alleviate certain types of cancer, type 2 diabetes and cardiovascular diseases.”

The irony is that there’s a GMO legume already on the market, soy, that has found its way into just about all processed and fried foods in the form of partially hydrogenated soybean oil (a.k.a. trans fat). Will the result of this research be a new GMO legume that treats diet-related diseases caused by other GMO legumes?

It would certainly be a first for the field of genetic engineering. In fact, any new GMO crop that actually improved the nutrition, health value, or stress-resistance of any crop would be a first. Contrary to popular belief, to date, there is not one consumer benefit associated with any GMO crop. They’re all genetically modified to either withstand or produce pesticides (usually manufactured by the chemical company that genetically engineered the crop).

The frightening thing is that the plan to create a genetically engineered legume that could reduce cholesterol and sugar levels would most likely be a pharma crop, a plant genetically engineered to produce a pharmaceutical. This is one of the most dangerous forms of genetic engineering. When grown outdoors on farmland, where most pharma crop trials have occurred, pharma crops can easily contaminate conventional and organic crops. In one chilling example from 2002, a corn crop engineered by ProdiGene to produce a vaccine for pigs contaminated 500,000 bushels of soybeans that were grown in the Nebraska field the next season. Before this incident, a similar thing had happened in Iowa where the USDA ordered ProdiGene to pay for the burning of 155 acres of conventional corn that may have cross-pollinated with some of the firm's biotech plants.

ProdiGene eventually went out of business, but not before it received a $6 million investment from the Governors Biotechnology Partnership, chaired by Iowa governor, Tom Vilsack, currently Shah's boss at the USDA. Vilsack didn't want any restrictions placed on experimental pharma crops. In reaction to suggestions that pharma crops should be kept away from food crops, Vilsack argued that "we should not overreact and hamstring this industry."

Roger Beachy, currently working under Shah as the USDA National Institute of Food and Agriculture director, joined Vilsack in support of ProdiGene and against regulation of pharma crops when he was still the director of Monsanto's research arm, the Danforth Center. He said in 2004 that scientists must be free to experiment in open fields:

"A ban would significantly halt the technology of producing drugs more cheaply in plants" than through current methods, Beachy said. And if work on biopharming to grow industrial chemicals were halted, "then you have stopped another kind of advance that we're looking for to give an economic advantage to our farmers."


In other news, the USDA announced on November 2, 2009, that an international team of scientists funded with a $10 million USDA grant has completed its first draft of the genome of a domesticated pig.

“Understanding the swine genome will lead to health advancements in the swine population and accelerate the development of vaccinations for pigs,” said Roger Beachy, NIFA director. “This new insight into the genetic makeup of the swine population can help reduce disease and enable medical advancements in both pigs and humans.”

And, it would aid Monsanto in their effort to patent pigs .
believe_it
Again, see post #154:

Do you think other nations will demand scientific proof that GMO containing foods do not harm children before introducing them into the food supply?


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QUOTE
http://www.huffingtonpost.com/andrew-kimbr...m_b_362888.html

New Report: GMOs Causing Massive Pesticide Pollution

Andrew Kimbrel, Executive Director of the Center for Food Safety
Posted: November 21, 2009 05:50 PM


There is one fact about genetically engineered foods that there is no debate about: no one wakes up in the morning eager to buy gene-altered food. There's good reason for this. Genetically modified foods do nothing for the "eating public". They provide no extra nutrition, flavor, safety or any other trait that people actually want. Instead, these food products only offer risks, which include potential toxicity, allergenecity, and lower nutritional value.

This presents a tough problem for the Monsantos of the world, who are pushing these GM foods. How can you sell something to the public that offers no benefits to them? And, because of their lobbying power, the biotech companies have ensured that their products are not labeled. So Monsanto's real request of the public is "be unknowing guinea pigs for foods that make us a lot of money and offer you nothing but risk."

Obviously this message is a PR nightmare, so Monsanto has come up with a spin that is old as public relations itself: "accept and buy our products because they will help the world." More particularly, their ads displayed in mass transit systems around the country and regularly on NPR claim that GM foods "will feed a hungry world" and "reduce the load of pesticides" used in agriculture.

Not surprisingly, both these claims turn out to be self-serving myths. Earlier this year the Union of Concerned Scientists issued a detailed report entitled "Failure to Yield". The report's findings were straightforward and incontrovertible. After 21 years of research, billions of dollars of investments in public and private funds, and more than 13 years of commercialization, GM crops have done nothing to significantly increase yield: so much for the "feeding the world's hungry" spin.

Now, a new report from The Organic Center, "Impacts of Genetically Engineered Crops on Pesticide Use: The First Thirteen Years", exposes the "less pesticide" myth. The report, which was released on Tuesday, was authored by Dr. Charles Benbrook, a leading agricultural scientist. In the spirit of full disclosure, I should also mention that Center for Food Safety helped fund the report.

It turns out that far from reducing pesticides, GM crops are a major reason for the massive expansion of pesticide use in recent years. This should not be a surprise. The majority of GE crops are "Roundup Ready," designed to survive heavy and repeated spraying with Monsanto's Roundup weedkiller. Roundup Ready crops have dramatically increased Roundup use, and spawned a growing epidemic of Roundup-resistant weeds, which now infest millions of acres of American cropland. Killing resistant weeds requires more herbicides. How much more? Dr. Benbrook's study - based on official USDA data - shows that GE crops have increased the overall use of weedkillers in the U.S. by a massive 383 million pounds since 1996.

Sometimes even more chemicals won't do the trick. In the South, cotton farmers are reverting to the pre-industrial practice of "chopping cotton," or manual hoeing, to rid their fields of Roundup-resistant pigweed.

Never fear, the biotech industry has "killer" solutions to the Roundup-resistant weed epidemic - you guessed it, new crops resistant to different and multiple herbicides. Dr. Benbrook describes these "next-generation" GE crops, which are the true pesticide-promoting future of agricultural biotechnology.

For instance, Dow Agrosciences will soon bring us GE corn, resistant to 2,4-D, one of the weedkillers in Agent Orange - the dioxin-laced defoliant used during the Vietnam War. 2,4-D-resistant corn will undoubtedly increase use of this dangerous weedkiller, which has been banned in Sweden, Norway and Denmark due to its links to cancer and reproductive disorders. Monsanto, DuPont, Bayer and Syngenta all have their own new "herbicide-tolerant" crops in the works, some resistant to two and even three herbicides each. The inevitable result will be continuing increases in the use of toxic chemicals to kill "next-generation" weeds resistant to multiple weedkillers.

In the face of all this, many farmers are becoming disillusioned with GE crops. In many states, demand for conventional seed, especially soybeans, is outstripping supply. Among the reasons given by farmers for this historic switch are dramatic price hikes for biotech seeds, increased pesticide costs due to resistant weeds, premiums for non-GM supplies, and importantly, the ability to save and replant conventional seeds, which is illegal with Monsanto's patented GE seeds.

Thanks then to the Union of Concerned Scientists and the Organic Center for debunking the myths about GM crops and foods. In terms of timing, the two reports released this year couldn't have come at a more crucial moment. Through careful scientific analysis they expose the false advertising that biotechnology companies are using in print and on our public radio airways.

We should all know what Monsanto and other companies are selling, and its not a solution to world hunger or a cleanser for the environment. What they are really selling is what they make best: chemicals. The biotech giants - Monsanto, DuPont, Syngenta, Bayer and Dow - are, without exception, major pesticide manufacturers. They have each bought up sizeable chunks of the world's seed supply, and are using biotechnology to make those seeds sell their pesticides for them.

It may be good for their bottom line, but its bad for us, the safety of our food, and the health of our environment.

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QUOTE
http://www.seedsofdeception.com/utility/sh.../?objectID=4091

Press Notice
9 November 2009


MONSANTO PULLS GM CORN AMID SERIOUS FOOD SAFETY CONCERNS

Applicant's dossiers contained wide-ranging fraudulent research

For the first time, a GM multinational has pulled two GM corn varieties from the regulatory and assessment process at the eleventh hour (1), after planning for a future income of several billion dollars per year from global sales (2). Monsanto has abandoned its ambitious plans for a so-called "second generation GM crop" rather than accede to a request from European regulators for additional research and safety data (3).

Under conditions of great secrecy, Monsanto has informed EFSA that it no longer wishes to pursue its application for approval of GM maize LY038 and the stacked variety LY038 x MON810. Both of these varieties were designed to accelerate the growth rate of animals. Two letters were sent to EFSA from the Monsanto subsidiary company Renessen at the end of April this year confirming the withdrawal of its applications originally submitted in 2005 and 2006. The letters cite "decreased commercial value worldwide" and state that the high-lysene varieties "will no longer be a part of the Renessen business strategy in the near future." (4) There has been no announcement of these decisions on the Monsanto web site, and there are no mentions on EFSA or European Commission web sites either. In other words, there is a conspiracy of silence involving both the applicants and the regulators.

The two letters sent to EFSA in April requested the return of all dossier material (varietal characterization, experimental protocols, and test results) which was submitted with the applications for cultivation, animal feed and human food (4). EFSA acceded to this request, making it impossible for any future independent researchers to analyse the Monsanto / Renessen data. That in itself is profoundly disturbing.

Scientists who have followed these two applications are quite convinced that the "decisions to withdraw" have nothing to do with commercial considerations and everything to do with food safety. In other words, the varieties are too dangerous to be allowed onto the open market -- although they would certainly have been approved by EFSA and most other European regulatory authorities had it not been for the diligence of independent scientists in New Zealand who subjected the application dossiers to very close scrutiny (5). In the absence of such scrutiny in the United States, the varieties were approved in 2005 for cultivation, animal feed and human food use on the other side of the Atlantic (6). Consents for food and feed use were also given in Japan, Canada, the Philippines, and South Korea. In 2007 Food Standards Australia and New Zealand (FSANZ) approved LY038 for food and feed use in spite of strenuous objections from the Green Party and scientists at Canterbury University's Centre for Integrated Research in Biosafety (INBI) who warned that the new corn was not safe for humans when cooked (7). They also expressed concerns about unpredictable health effects, increased levels of toxins in high-lysene corn, and possible allergies and links to cancer.

It does not appear that the varieties have been grown or "commercialized" anywhere in the world (8), although test plantings probably occurred in the United States.

"Blatant scientific fraud by the applicants"

While INBI's detailed and devastating analysis of the applicant's supporting dossiers was dismissed out of hand by FSANZ, EFSA was forced to take it seriously because of concerns from a large number of European countries including Finland and Malta. The scientific bases of those concerns were highlighted by Jeffrey Smith in his book "Genetic Roulette" and by Prof Jack Heinemann in his book "Hope not Hype" (9). The Monsanto dossiers included rigged research and false assumptions in the reported experiments; a failure to offer any test results based on cooked or processed corn; a failure to test the whole GM plant in feeding trials; confusing and contradictory characterizations of the GM varieties and proteins; a fraudulent mixing of GM strains during trials; a pooling of crop data so as to mask undesirable effects in experiments; feeding trials too short to reveal true physiological changes in animal tissues; and the choice of an irrelevant, unrelated corn variety as the control group for comparison with the GM lines, with the clear intention of hiding potentially serious differences in composition or side effects on animals(10). The Codex guidelines for the testing of GM crops were thus comprehensively broken by Monsanto's subsidiary Renessen, and were not enforced by the regulators in the USA, Canada, Australia and New Zealand (11). All in all, this amounted to blatant scientific fraud by the applicants, and a cynical failure to enforce the rules, and to protect the public, by the regulators.

During the assessments of these two varieties in Europe, many countries used the INBI peer review of the applicant's dossiers to underpin their concerns, and these widely-expressed concerns forced EFSA to ask the applicants for additional studies and for a clarification of their experimental data (12). EFSA also asked -- for the first time -- for adherence to the Codex rules relating to GM and comparator studies. In the knowledge that their dossiers were now being subjected to an unprecedented level of scrutiny, Monsanto / Renessen simply decided that they would not cooperate in this process for fear of what might emerge. So they wrote to EFSA in April (4) to indicate that they were abandoning all plans for the cultivation and commercialization of the two GM crops.

"EFSA has been unfit for purpose"

Commenting for GM-Free Cymru, Dr Brian John said: "This is the first time, to our knowledge, that EFSA has sought to enforce the Codex rules relating to the use of isolines in the testing of GM crops, and the first time that it has expressed profound dissatisfaction about the content of an applicant's dossiers. It is also the first time that a GM multinational has withdrawn a GM product (or two products) at the eleventh hour. It was insane in the first place to seek to pass GM maize crops containing Bt toxins and "growth enhancers" straight into the human food chain (13). In addition, EFSA and the other regulators have been quite irresponsible in the past in assuming that "stacked" events, hybridized from two GM lines, are harmless if the applicant says so, and if the separate lines have been independently approved. That is simply bad science, since it fails to address the likelihood of synergistic effects and even accumulating toxins in the food chain (14).

"Nonetheless, we applaud the fact that EFSA has asked Monsanto some hard questions in this case, having in the past demonstrated, over and again, that its GMO Panel is simply unfit for purpose (15). This represents progress.

"We are quite convinced that Monsanto has been fully aware, from the beginning, that line LY038 and line LY038 x MON810 are both dangerous; and yet they persisted with their applications until the extent of their scientific fraud was exposed to the public. We should not be surprised by this. The corporation pushes dangerous products onto the food market all the time, and does whatever is necessary to hoodwink the regulators into the belief that all is well (16). We are convinced that Mansanto has other in-house studies which show that these varieties are unstable, unpredictable and harmful to health. Will we ever get to see these studies? No way!"

NOTES

(1) Based on information released under the Freedom of Information legislation. GM Free Cymru holds a folder containing all the key documents referred to in this Press Notice. GM crops have been "pulled" or withdrawn before -- for example the maize called Chardon LL -- but this is the first time this has happened specifically because of a request for new safety data from the regulators.

(2) http://www.stuff.co.nz/national/3020246/Eu...t-GE-corn-in-NZ
This article highlights the key role played, over several years, by Prof Jack Heinemann and his team at Canterbury University's Centre for Integrated Research in Biosafety (INBI) in revealing the shortcomings of the Monsanto applications.

(3) http://www.gmo-compass.org/eng/gmo/db/86.docu.html
"Second generation" GM crops, including those with supposedly enhanced nutritional value, are likely to be non-uniform and unstable because they have complex introduced traits. If two or more GM lines are hybridized to introduce "stacked" GM traits, the potential dangers become even greater because of synergistic effects. In spite of this, regulators simply assume them to be safe if the parental lines themselves have been approved for cultivation or food or feed use.
See: The Problem with Nutritionally Enhanced Plants, by David R. Schubert. Journal of Medicinal Food. December 2008, 11(4): 601-605.
http://www.liebertonline.com/doi/abs/10.1089/jmf.2008.0094
http://www.gmfreecymru.org/pivotal_papers/problem.htm
http://www.bioscienceresource.org/docs/BSR-2-BGERvol23.pdf
Transformation-induced Mutations in Transgenic Plants: Analysis and Biosafety Implications, by Allison K Wlson, Jonathan R Latham and Ricarda A Steinbrecher. Bioscience Resource Project.
The work of these independent scientists on so-called "genome scrambling" reveals how the genetic engineering of crops not only lacks precision but causes large scale genetic rearrangements of host DNA at transgene insertion sites, as well as large numbers of mutations scattered throughout the genome of each new transgenic plant. The significance of all this genetic damage is that the food safety of edible crops relies crucially on genetic stability.
http://www.i-sis.org.uk/GE-maize.php

(4) These letters are available as PDFs on request.
Brussels, 30 April 2009, from Renessen Europe SPRL
Re: Application for authorisation of genetically modified LY038 maize submitted IIIlder
Regulation (EC) No 1829/2003 - Withdrawal of Application EFSA-GMO-NL-2006-31
Brussels, 30 April 2009, from Renessen Europe SPRL
Re: Application for authorisation of genetically modified LY038 x MON810 maize submitted IIIlder
Regulation (EC) No 1829/2003 - Withdrawal of Application EFSA-GMO-NL-2006-32

(5) Submissions to FSANZ from INBI relating to the dossier for LY038:
Cretenet, M., Goven, J., Heinemann, J.A., Moore, B. and Rodriguez-Beltran, C.
2006. Submission on the DAR for Application A549 Food Derived from High-Lysine
Corm LY038: to permit the use in food of high-lysine corn. http://www.inbi.canterbury.ac.nz

(6) Lucas,D. Petition for determination of nonregulated status for lysine maize LY038 -- USDA/APHIS 2004 http://www.aphis.usda.gov/brs/aphisdocs/04_22901p.pdf
Agbios database for LY038 and LY038 + MON810. Site currently designated as high risk.
http://www.biosafety-info.net/bioart.php?bid=358
High lysine corn (LY038) deregulated in the US, but safety still in doubt
Why Not Transgenic High Lysine Maize by Professor Joe Cummins, ISIS Report 23/11/05
http://www.i-sis.org.uk/highlysinemaize.php

(7) http://www.greens.org.nz/press-releases/nz...pproval-ge-food

(8) http://www.biotradestatus.com/default.cfm

(9) Jeffrey Smith: "Genetic Roulette", pp 102-105 and Part 3, p 194
http://www.seedsofdeception.com/utility/sh...e/?objectID=892
Jack Heinemann: "Hope not Hype", see Chapter 4
https://sites.google.com/site/therightbiotechnology/

(10) Submission on APPLICATION A549 FOOD DERIVED FROM HIGH LYSINE CORN LY038: to permit the use in food of high lysine corn ----- Submitted to Food Standards Australia/New Zealand (FSANZ)
by New Zealand Institute of Gene Ecology
January 22, 2005

(11) Joint FAO/WHO Food Standards Programme. Codex Alimentarius Commission. Procedural Manual. 12th ed.
Rome: Food and Agriculture Organization of the United Nations : World Health Organization, 2001. Available
online http://www.fao.org/DOCREP/005/Y2200E/y2200e00.htm. Access date 31 May 2006.

(12) Letter from EFSA to Monsanto / Renessen -- Ref: Ref. PB/AC/ mt (2009) 3826240 and the Member States' comments submitted during the three-month consultation period on this application.

(13) http://www.biosafety-info.net/bioart.php?bid=358

(14) SMARTSTAX APPROVAL IGNORED RISKS
http://www.gmwatch.org/index.php?option=co...l-ignored-risks
http://www.organicconsumers.org/articles/article_18717.cfm
http://www.foeeurope.org/GMOs/Seeds.htm
Austrian Federal Department for Health: "A stacked organism has to be regarded as a new event, even if no new modifications have been introduced. The gene?cassette combination is new and only minor conclusions could be drawn from the assessment of the parental lines, since unexpected effects (e.g. synergistic effects of the newly introduced proteins) cannot automatically be excluded. Furthermore, it should not be neglected that two of the parental lines, GM maize MON89034 and GM maize MON88017, have not yet gained authorisation within the European Union."
http://www.gmwatch.org/latest-listing/1-ne...tstax-in-europe

(15) http://www.gmfreecymru.org/open_letters/Op...er10Dec2007.htm
OPEN LETTER, "EFSA is not fit for purpose "
From GM-Free Cymru to Catherine Geslain-Laneelle Executive Director, EFSA Parma Italy, 10th December 2007

(16) http://www.gmfreecymru.org/pivotal_papers/quotes.html
More evidence of Scientific Malpractice in GM assessment process
Under wraps
NATURE BIOTECHNOLOGY, VOLUME 27, NUMBER 10, October 2009 http://www.emilywaltz.com/Biotech_crop_res...ns_Oct_2009.pdf
The Genetic Engineering of Food and the Failure of Science – Part 2: Academic Capitalism and the Loss of Scientific Integrity
by Don Lotter Int. Jrnl. of Soc. of Agr. & Food, Vol. 16, No. 1, pp. 50–68
http://www.gmfreecymru.org/pivotal_papers/...capitalism.html
Exposed: Monsanto's fraudulent safety tests for GM Soy
http://www.gmfreecymru.org/pivotal_papers/exposed.htm
Abuse of the Scientific Method Seen in Monsanto Aspartame Research
http://www.holisticmed.com/aspartame/abuse/
Criminal Investigation of Monsanto Corporation - Cover-up of Dioxin Contamination in Products - Falsification of Dioxin Health Studies.
http://www.purefood.org/dioxcov.html


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QUOTE
http://www.gmfreecymru.org/pivotal_papers/quotes.html

Scientists speak out against GM science fraud

(Note from GM Free Cymru -- most of these quotes are quite old. But nothing has changed. If anything, the situation has got worse during the last decade, as we show consistently on this site.)

Commercial influence on science http://www.bangmfood.org/quotes/24-quotes/...ence-on-science

"When we spliced the profit gene into academic culture, we created a new organism - the recombinant university. We reprogrammed the incentives that guide science. The rule in academe used to be 'publish or perish'. Now bioscientists have an alternative - 'patent and profit'." Tom Abate, "Scientists' 'publish or perish' credo now 'patent and profit'", San Francisco Chronicle, 13 August 2001

"The universities are cheering us on, telling us to get closer to industry, encouraging us to consult with big business. The bottom line is to improve the corporate bottom line. It’s the way we move up, get strokes.... We can’t help but be influenced from time to time by our desire to see certain results happen in the lab. All of these companies have a piece of me. I'm getting checks waved at me from Monsanto and American Cyanamid and Dow, and it's hard to balance the public interest with the private interest. It’s a very difficult juggling act, and sometimes I don’t know how to juggle it at all." John Benedict, Texas A&M University entomologist, quoted in Susan Benson, Mark Arax and Rachel Burstein, “A Growing Concern”, Mother Jones, January/February 1997

"There is a great deal of potential research investment in the UK that could come from food technology industries, and any concerns about the safety of these foods could jeopardise this huge investment. So I can understand why scientists would be very anxious about jeopardising that investment." Dr Richard Horton, editor of the Lancet, Channel 4 News, 15 October 1999

"These competing interests are very important. It has quite a profound influence on the conclusions and we deceive ourselves if we think science is wholly impartial." Dr Richard Smith, editor of the British Medical Journal, quoted in Liz Lightfoot, “Scientists ‘asked to fix results for backer’”, Daily Telegraph, 14 February 2000

"All policymakers must be vigilant to the possibility of research data being manipulated by corporate bodies and of scientific colleagues being seduced by the material charms of industry. Trust is no defence against an aggressively deceptive corporate sector." Editorial, The Lancet, quoted in Sarah Boseley, “$2m plot to discredit smoking study exposed”, The Guardian, April 7 2000

"A survey measuring attitudes toward biotechnology among Cornell University agricultural and nutrition-science faculty and extension staff (who advise farmers) found that nearly half have reservations about the health, safety, and environmental impacts of genetically engineered food crops and doubt they are the answer to global hunger. Though their numbers were fewer, the biotech promoters said they felt very comfortable publicly voicing their views, while the concerned majority did not express that sentiment." Karen Charman, “Spinning Science into Gold”, Sierra Magazine, July/ August 2000

"Public health professionals need to be aware that the 'sound science' movement is not an indigenous effort from within the profession to improve the quality of scientific discourse, but reflects sophisticated public relations campaigns controlled by industry executives and lawyers whose aim is to manipulate the standards of scientific proof to serve the corporate interests of their clients." Dr Stanton Glantz and Dr Elisa Ong, “Constructing ‘Sound Science’ and ‘Good Epidemiology’: Tobacco, Lawyers, and Public Relations Firms”, American Journal of Public Health, November 2001, Vol. 91, No. 11, pp. 1749-1757

"One in three scientists working for Government quangos or newly privatised laboratories says he has been asked to adjust his conclusions to suit his sponsor…. [Charles Harvey, spokesman, The Institute of Professionals, Managers and Specialists, said,] ‘The piper is calling the tune and it raises worrying issues. We have seen the BSE crisis, food scares and the GMO debacle and the public is losing confidence in Government as an independent, fair-minded arbiter.’” Liz Lightfoot, “Scientists ‘asked to fix results for backer’”, Daily Telegraph, 14 February 2000

"This is confirmation of all our worst fears that the Government’s GM policy is being driven by bad or fraudulent science. They are reliant on the industry that wants to sell these seeds to monitor the trials. This is insane, and criminally irresponsible. If data from one company has been falsified how do we know others have not been up to the same." Alan Simpson, UK Member of Parliament, quoted in Antony Barnett, “Revealed: GM firm faked test figures: Poor crop results were replaced by a forgery, Ministry’s internal paper shows”, The Observer, April 16 2000

"History has shown that meaningful assessment of cost as well as benefit issues is unlikely when technology assessment is provided by proponents who have a clear vested interest in the adoption of the technology." Dr E. Ann Clark, associate professor, department of plant agriculture, University of Guelph, Canada, “Genetic Engineering in Field Crops: Ethics and Academia”, paper presented to the Annual Meeting of the Saskatchewan Institute of Agrologists, April 1999

"There is too much hype. Every gene that is discovered will lead to a cure for cancer." Dr Maxine Singer, the National Academy of Sciences, quoted in "Big Science: Bloated, Whiny and Self-Important", Scientific American, September 2001

"I think there is a very real problem from the point of view of university research in the way that private companies have entered the university, both with direct companies in the universities and with contracts to university researchers. So that in fact the whole climate of what might be open and independent scientific research has disappeared, the old idea that universities were a place of independence has gone. Instead of which one’s got secrecy, one’s got patents, one’s got contracts and one’s got shareholders." Prof Steven Rose, professor and chairman of the department of biology, Open University, quoted in “Science Fact or Fraud?”, BBC World Service, 15 September 2000

"The independent scientist who conducts research for the public good 'barely exists any more,' according to one leading expert on technology and public policy. 'They get up and talk as if they are neutral. But they almost always have some share in the company or some self-interested gain for their work,' said Philip Bereano, a professor from the University of Washington in Seattle." Les Perreaux and Sandra Rubin, "Courts last defence against scientific 'elite': professor", National Post, 14 August 2001

"For any scientist who wants a good job and a nice home with mortgage payments, he's not going to choose the Union of Concerned Scientists." Dr Hugh Gusterson, MIT, quoted in Kristina Canizares, "Science Good, Nature Bad: The Biotech Dogma", AlterNet, June 26 2001

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http://lifehealthchoices.com/index.php



FYI dual purpose post (links below from same homepage as GMO food photo above): laugh.gif I really don't want to start another thread.
NJ Suspends Vax Mandate 11/24/09
New Jersey today suspended enforcement of its first-in-the-nation mandate that preschoolers receive seasonal flu vaccine in order to attend licensed preschool and childcare...

AMA: Yes To Vax Choice 11/23/09
The AMA House of Delegates rejected a proposal to mandate vaccinations for health care professionals...
believe_it
QUOTE
http://www.organicconsumers.org/articles/article_19789.cfm

(A lot of busted links on this story, always interesting to chase down)
http://74.125.93.132/search?q=cache:DCgsBK...=clnk&gl=us

Austrian scientist confirms GMO maize unsafe
// added December 06, 2009 // 29 comments //

http://hejdagmo.files.wordpress.com/2009/1...trian-study.pdf

NOTE: Many thanks to Akiko Frid for making available these comments on the safety of Monsanto's GMO-maize by the Austrian scientist Dr Alberta Velimirov.

EXTRACT: "But whatever statistical analyses might or might not be used, the data are always the same and open for everybody to see. This study gives the first indication that the stacked event MON810xNK603 led to a reduced reproductive performance as compared to the non-GM line. This result should not be dismissed as 'bad science' but discussed on a scientific level and taken up as incentive to continue investigations in this direction with other GM crops." - Dr Alberta Velimirov

BACKGROUND: In November 2008 the Austrian Ministry of Health publicly released the results of a study it had commissioned to investigate long term reproductive effects in mice following dietary exposure to a genetically modified (GM) stacked maize NK603xMON810.

STUDY SUMMARY OF FINDNGS: Mice fed GM insecticide-producing maize over four generations showed a buildup of abnormal structural changes in various organs (liver, spleen, pancreas), major changes in the pattern of gene function in the gut, reflecting disturbances in the chemistry of this organ system (e.g. in cholesterol production, protein production and breakdown), and, most significantly, reduced fertility.

REF: Biological effects of transgenic maize NK603xMON810 fed in long term reproduction studies in mice. Velimirov A et al. Bundesministerium für Gesundheit, Familie und Jugend Report, Forschungsberichte der Sektion IV Band 3/2008, Austria, 2008. http://bmgfj.cms.apa.at/cms/site/attachments/3/2/9/ CH0810/CMS1226492832306/forschungsbericht_3-2008_letztfassung.pdf

Subsequently two hostile criticisms of the study by ‘regulators’ - EFSA GMO Panel and FSANZ - have been published. Here we present criticisms from each and then Dr. Velimirov's response...

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http://www.gmwatch.org/latest-listing/1-ne...rt-peace-prize-

Pusztai to receive Stuttgart Peace Prize

Friday, 11 December 2009 10:52

We've just heard that Dr Arpad Pusztai and Dr Susan Bardocz will be presented with this year's Stuttgart Peace Prize. The award is for their tireless advocacy for independent risk research. Both have made an essential contribution to a broader understanding of the dangers of genetic manipulation. The award also honours their courage and scientific integrity as well as their undaunted insistence on the public's right to know.

The award will take place on 18 December with a Film and Book launch at 4 pm and a Peace Gala at 7:30 pm, at the Theaterhaus Stuttgart.

More details (in German) here:
http://www.gentechnikfreies-europa.eu/

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Below is a profile of Dr Pusztai and how he changed the GM debate (from above link).

QUOTE
http://www.spinprofiles.org/index.php/Arpad_Pusztai

Arpad Pusztai

The history of events and the quotes below are adapted from Andy Rowell's book, Don't Worry, It's Safe to Eat, Earthscan, 2003, ISBN 1853839329.

On 10 August 1998 the GM debate changed forever with the broadcast of a programme on British TV about GM food safety featuring a brief but revealing interview with Dr Arpad Pusztai about his research into GM food safety. Dr Pusztai told of his findings on the ill effects of GM potatoes on laboratory rats. He was subsequently gagged and suspended by his institute, the Rowett Research Institute in Scotland, his research team was disbanded, and his research data was confiscated. He was subjected to a campaign of vilification and misrepresentation by several pro-GM scientific bodies and pro-GM lobbyists, in an attempt to discredit him and his research.

The story began three years earlier. That's when the UK government's Scottish Office commissioned a three-year multi-centre research programme into the safety of GM food under the coordination of Dr Arpad Pusztai. At that time there was not a single publication in a peer-reviewed journal on the safety of GM food.

Dr Pusztai, a Fellow of the Royal Society of Edinburgh, was an eminent scientist. He was the world's leading expert on the plant proteins known as lectins. He had published three books and over 270 scientific studies.

He and his team fought off competition from 28 other research organisations from across Europe to be awarded the GBP1.6 million contract by the Scottish Office. The project methodology was also reviewed and passed by the Biotechnology and Biological Sciences Research Council (BBSRC) - the UK government's main funding body for the biological sciences.

The research involved feeding GM potatoes to rats and monitoring physiological changes. By late 1997 preliminary results from the rat-feeding experiments were showing totally unexpected and worrying changes in the size and weight of the rat's body organs. Liver and heart sizes were getting smaller, and so was the brain. There were also indications that the rats' immune systems were weakening.

Dr Pusztai was interviewed for a programme about GM food being made by Granada TV's World in Action. The filming took place in late June 1998 with the agreement of the director of the Rowett Institute, Professor Philip James, and in the presence of the Rowett Institute's press officer. The World in Action interview was broadcast on the evening of Monday 10 August 1998.

Later that evening Professor James congratulated Dr Pusztai on his TV appearance, commenting on "how well Arpad had handled the questions". The next day a further press release from the Rowett noted that 'a range of carefully controlled studies underlie the basis of Dr Pusztai's concerns'. However, reportedly following two calls to the Rowett from the Prime Minister's Office, the Government, the Royal Society and the Rowett launched a vitriolic campaign to sack, silence and ridicule Dr Pusztai.

He was accused of unprofessional conduct because his work had not been peer-reviewed. However, his research subsequently passed peer-review after being reviewed by a larger than usual panel of scientists and was published (see below). Many people also take the view that in circumstances where research is giving rise to serious concerns that may need to be addressed sooner rather than later, it is acceptable for scientists to act as whistle blowers and draw attention to the problems their research is uncovering even prior to peer-reviewed publication.

The Government criticised the methodology of Pusztai's research despite the fact that this had been approved in advance by its own Biotechnology and Biological Sciences Research Council. Neither the Government nor any other official body has ever repeated or refined Dr Pusztai's experiments to test the validity of his results.

The Royal Society and its leading Fellows were key players in the attacks on Dr Pusztai from the time he went public with doubts about the safety of GM foods. In February 1999, for instance, nineteen Fellows of the Royal Society condemned Pusztai, in all but name, in a letter published in the national press. Among the signatories was Peter Lachmann, who played a key role in the attacks on Pusztai.

Three months later in May 1999 the Royal Society published a partial 'peer review' of Pusztai's then unpublished research. This review was based not on a properly prepared paper, like that Pusztai and his collaborator Ewen submitted to The Lancet for peer-review, but on a far-from-complete internal report intended for use by Pusztai's research team at the Rowett Institute.

Richard Horton, editor of The Lancet, described the Royal Society review as 'a gesture of breathtaking impertinence to the Rowett Institute scientists who should be judged only on the full and final publication of their work.'

The Royal Society's review was organised by members of a working group appointed by the Society in coordination with the Society's officers. The Royal Society claimed that anyone who had already commented on the Pusztai affair had been excluded from this decision making process in order to avoid bias. However, William Hill, Patrick Bateson, Brian Heap and Eric Ash, who were all involved, were all among the co-signatories of the letter condemning Pusztai that had been published in The Daily Telegraph back in February.

In addition, four key people involved, including the Chair of the working group, Noreen Murray, as well as Brian Heap, Rebecca Bowden and Sir Aaron Klug, were all part of the earlier working group that had issued the Royal Society's 1998 report supporting GM foods.

There were other issues of bias. For instance, William Hill, the chair of the Pusztai working group, was also the deputy chair of the Roslin Institute, famous for genetically modifying animals and for cloning Dolly the sheep. Roslin in turn had links to Geron Biomed for whom Lachmann consulted. Similarly, Noreen Murray was the wife of the co-founder of Europe's first biotechnology company, Biogen.

Undaunted by the Royal Society's attack on their unpublished work, Pusztai and his co-researcher, Prof Stanley Ewen, submitted their final paper on their experiments to The Lancet. It was sent to six reviewers, double the normal number, and a clear majority were in favour of its publication.

However, prior to publication the Lancet's editor Richard Horton received a phone call from Peter Lachmann, the former Vice-President of the Royal Society. According to Horton, Lachmann called him "immoral" for publishing something he knew to be 'untrue'. Towards the end of the conversation Horton says Lachmann also told him that if he published Pusztai's paper, this would "have implications for his personal position" as editor.

The Guardian broke the news of Horton being threatened in November 1999 in a front-page story. It quoted Horton saying that the Royal Society had acted like a Star Chamber over the Pusztai affair: "The Royal Society has absolutely no remit to conduct that sort of inquiry." Lachmann denied threatening Horton although he admitted making the phone call in order to discuss the pending publication.

The Guardian also talked of a GM 'rebuttal unit' operating from within the Royal Society. According to the journalist Andy Rowell, who helped research The Guardian article, Rebecca Bowden, who had coordinated the Pusztai peer-review and who had worked for the Government's Biotechnology Unit before joining The Royal Society in 1998, admitted to the paper, 'We have an organization that filters the news out there. It's really an information exchange to keep an eye on what's happening and to know what the government is having problems about … its just so that I know who to put up.'

The attacks on The Lancet editor and his decision to publish Pusztai's paper continued. Sir Aaron Klug, vigorously opposed the publication of Pusztai's research, saying it was fatally flawed in design because the protein content of the diets which control groups of rats were fed on was not the same as that of the other diets. Pusztai commented: 'In fact, the paper clearly states that ALL diets had the same protein content and were iso-energetic. I cannot assume that Sir Aaron is not sufficiently intelligent to read a simple statement as that, so the only conclusion I can come to is that he deliberately briefed the reporters with something that was untrue.'

Richard Horton remained unbowed. 'Stanley Ewen and Arpad Pusztai's research letter,' he wrote, 'was published on grounds of scientific merit, as well as public interest'. What Sir Aaron Klug from the Royal Society cannot 'defend is the reckless decision of the Royal Society to abandon the principles of due process in passing judgement on their work. To review and then publish criticism of these researchers' findings without publishing either their original data or their response was, at best, unfair and ill-judged'.

The attacks continue unabated. Peter Lachmann's successor as Biological Secretary of the Royal Society, Patrick Bateson, told readers of the British Association's journal Science and Public Affairs that The Lancet had only published Pusztai's research 'in the face of objections by its statistically-competent referees' (June 2002, Mavericks are not always right). Bateson, presumably deliberately, inverts the fact that Pusztai's Lancet paper successfully came through a peer review process that was far more stringent than that applying to most published papers.

In an article in The Independent, giving the Royal Society's views on why the public no longer trusts experts like themselves - 'Scientists blame media and fraud for fall in public trust' - Pusztai's work is categorised as 'fraud'. Pusztai's peer reviewers, we are told in the article, 'refused it for publication, citing numerous flaws in its methods - notably that the rats in the experiment had not been fed GM potatoes, but normal ones spiked with a toxin that GM potatoes might have made.' Almost every word of this is straight fabrication. There was no fraud. Rats were fed GM potatoes. The publication of Pusztai's Lancet paper was supported by a clear majority of its peer reviewers, etc. etc. It is particularly ironic that such a travesty should have been published in an article reporting the Royal Society's concerns about the reporting of science in the media.

In February 2002 a new Royal Society report on GM crops was published as an update to the Society's September 1998 report on GM. The expert group which produced it was much more broadly based than in '98 and the report took a noticeably more cautious line. 'British Scientists Turn on GM Foods', ran The Guardian's headline on a report which included an admission 'that GM technology could lead to... unpredicted harmful changes in the nutritional status of foods'.

The expert group was chaired by Jim Smith, who had sat on the Society's Pusztai working group, and tucked away inside the report was a paragraph on Pusztai. Once again, it was designed to mislead.

The first part of the paragraph read: 'In June 1999, the Royal Society published a report, review of data on possible toxicity of GM potatoes, in response to claims made by Dr Pusztai (Ewen and Pusztai, 1999). The report found that Dr Pusztai had produced no convincing evidence of adverse effects from GM potatoes on the growth of rats or their immune function.’

The Royal Society report references the phrase 'claims made by Dr Pusztai' - claims it said it had reviewed - to the article published by Pusztai and Ewen in The Lancet in 1999. In fact, however, the Royal Society’s partial review of Pusztai's research was published months before The Lancet article appeared. The Royal Society thus conceals the fact that it had only ever reviewed part of Pusztai's data, condemning him ahead of publication of his actual paper.

The 2002 report continued: 'It concluded that the only way to clarify Dr Pusztai's claims would be to refine his experimental design and carry out further studies to test clearly defined hypotheses focused on the specific effects reported by him. Such studies, on the results of feeding GM sweet peppers and GM tomatoes to rats, and GM soya to mice and rats, have now been completed and no adverse effects have been found (Gasson and Burke, 2001).'

But the Gasson and Burke paper, to which these further feeding studies are referenced by the Society, was not a piece of primary research but an 'opinion' piece written by two pro-GM scientists, Mike Gasson and Derek Burke. Worse, one of t he two further studies mentioned had not even been published, except by way of summary, ie it had never been fully peer-reviewed. In other words, the Royal Society uses an unpublished and un-peer-reviewed study to attack Pusztai, two years after it had condemned him for speaking to the media without first publishing peer-reviewed work.

In response to criticism, the Royal Society admitted that the work in question remained unpublished but said this was not a problem because, 'it had been discussed at international scientific conferences'. By this definition, however, Pusztai's research would have been equally validated before the Society ever launched its partial review as it had been presented at an international conference prior to the Society's review. Curiously, the Royal Society has also described the opinion piece by Gasson and Burke as 'primary research,' even though it is a literature review involving no lab work.

Andy Rowell, author of a book that deals extensively with the Royal Society's role in the Pusztai affair, writes, 'the fundamental flaw in the scientific establishment's response is not that they try and damn Pusztai with unpublished data, nor is it that they have overlooked published studies [supporting Pusztai's concerns], but that in 1999, everyone agreed that more work was needed. Three years later, that work remains to be undertaken... [A] scientific body, like The Royal Society, that allocates millions in research funds every year, could have funded a repeat of Pusztai's experiments.'

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Dr Pusztai on the 10th anniversary of GM safety scandal

The following is an email - of 10 August 2008 from Dr Pusztai to Claire Robinson and Jonathan Matthews of GMWatch , in which Dr Pusztai comments on the 10th anniversary of the television interview.

Dear Claire and Jonathan,

I thought that I should write to you on the 10th anniversary of my 150 seconds of TV "fame" and tell you what I think now. It is very appropriate to write to you because you have provided the most comprehensive service to inform people about the shenanigans of the GM biotechnology industry and its advocates.

On this anniversary I have to admit that, unfortunately, not much has changed since 1998. In one of the few sentences I said in my broadcast ten years ago, I asked for a credible GM testing protocol to be established that would be acceptable to the majority of scientists and to people in general. 10 years on we still haven't got one. Instead, in Europe we have an unelected EFSA GMO Panel with no clear responsibility to European consumers, which invariably underwrites the safety of whatever product the GM biotech industry is pushing onto us.

All of us asked for independent, transparent and inclusive research into the safety of GM plants, and particularly those used in foods. There is not much sign of this either. There are still "many opinions but very few data"; less than three dozen peer-reviewed scientific papers have been published describing the results of work relating to GM safety that could actually be regarded as being of an academic standard; and the majority of even these is from industry-supported labs. Instead we have the likes of Tony Trewavas and others writing unsupported claims for the safety of GM food and defaming people like Rachel Carson who can no longer defend herself; not that she needs to be defended from such nonentities.

In normal times one would not pay much attention to such people desperately trying to be seen as the advocates of true science, but these are not normal times. The mostly engineered (GM engineered) food crisis gives the GM biotech industry and its warriors an opportunity to come to the fore with claims that GM is the only way to save a hungry world; a claim not much supported by responsible bodies, such as the IAASTD. The advocates of GM also now think that they have found a chink in the armory of people's resolve that they can exploit by telling us that we would not be able to feed our animals without GM feedstuffs. In this way, they hope to bring in GM by the backdoor. Please remember that whatever our animals eat, we shall also get back indirectly. Rather ominously, there has been no work whatever to show the safety of the meat of GM-fed animals.

We must not underestimate the financial and political clout of the GM biotechnology industry. Most of our politicians are committed to the successful introduction of GM foods. We must therefore use all means at our disposal to show people the shallowness of these claims by the industry and the lack of credible science behind them, and then trust to people's good sense, just as in 1998, to see through the falseness of the claims for the safety of untested GM foods.

Let's hope that on the 20th anniversary I shall not have to write another warning letter about the dangers of untested GM foods!

Best wishes to all
Arpad Pusztai

--

Biography

Dr Pusztai has a PhD from the University of London in biochemistry and physiology, and is former senior scientist at the Rowett Research Institute, Aberdeen, Scotland. Dr Pusztai was dismissed from the Rowett Research Institute after he went public with his research on GM potatoes in 1998. The research was finally published in The Lancet in 1999.

In 2005, Dr Pusztai was honoured with a whistleblower award from the Federation of German Scientists. Since his research was made public he has given close to 200 lectures across the world.

Resources

Interview with Dr Arpad Pusztai about his experimental findings on GM potatoes and the subsequent political fallout.

Arpad Pusztai and the Risks of Genetic Engineering, interview with Arpad Pusztai by Ken Roseboro, The Organic and Non-GMO Report, June 2009
http://www.organicconsumers.org/articles/article_18101.cfm

Notes

1. Andy Rowell, Don't Worry: Its Safe To Eat, Earthscan, 2003, ISBN 1853839329. See also: http://www.lobbywatch.org/profile1.asp?PrId=113


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QUOTE
http://www.gmwatch.org/latest-listing/1-ne...os-found-unsafe

Three Major GMOs Approved for Food and Feed Found Unsafe
(Int J Biol Sci 2009; 5(7), 706-726)
CRIIGEN press release, 11 December 2009


NOTE: The new paper is available here:
http://www.biolsci.org/v05p0706.htm
A Comparison of the Effects of Three GM Corn Varieties on Mammalian Health
Joël Spiroux de Vendômois1, François Roullier1, Dominique Cellier1,2, Gilles-Eric Séralini1,3 ✉
1. CRIIGEN, 40 rue Monceau, 75008 Paris, France
2. University of Rouen LITIS EA 4108, 76821 Mont-Saint-Aignan, France
3. University of Caen, Institute of Biology, Risk Pole CNRS, EA 2608, 14032 Caen, France


How to cite this article:
de Vendômois JS, Roullier F, Cellier D, Séralini GE. A Comparison of the Effects of Three GM Corn Varieties on Mammalian Health. Int J Biol Sci 2009; 5:706-726. Available from http://www.biolsci.org/v05p0706.htm

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QUOTE
http://www.ageofautism.com/2009/12/jb-hand...-gene.html#more

...quote from Dr. Francis Collins, current Director of the entire National Institutes of Health:

“Genes alone do not tell the whole story. Recent increases in chronic diseases like diabetes, childhood asthma, obesity or autism cannot be due to major shifts in the human gene pool as those changes take much more time to occur. They must be due to changes in the environment, including diet* and physical activity, which may produce disease in genetically predisposed persons."


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*hopefully, that benign sounding term includes BIOTECH FOOD, otherwise known as GMO, so-called 'food disparagement' laws notwithstanding.
believe_it
QUOTE
http://fanaticcook.blogspot.com/2009/10/ir...o-ban-gmos.html

Wednesday, October 14, 2009

Ireland To Ban GMOs

How about that, Ireland just went GM free. (The map to the right will have to be updated.) Here's a press release from GMFreeIreland.org (pdf):
Ireland Adopts Gm-Free Zone Policy
"The Irish Government will ban the cultivation of all GM crops and introduce a voluntary GM-free label for food – including meat, poultry, eggs, fish, crustaceans, and dairy produce made without the use of GM animal feed."
It looks like the Irish government is doing this not for reasons of science or ethics, although those are promotable effects, but for money.

With an increasing demand for non-GMO foods, and a decreasing world supply owing to agriculture dominance by US, Brazilian, and Argentine GMOs, Ireland sees this as an opportunity to fill a niche.

As an island, they're in a unique position to resist contamination from GM fields. Their livestock are already raised primarily on grass instead of GM feed. And they were having a tough time competing with the big producers anyway:

"The WTO’s economic globalisation agenda has forced most Irish farmers to enter an unwinnable race to the bottom for low quality GM-fed meat and dairy produce, in competition with countries like the USA, Argentina and Brazil which can easily out-compete us with their highly subsidised GM crop monocultures, cheap fossil fuel, extensive use of toxic agrochemicals that are not up to EU standards, and underpaid migrant farm labour."

Interesting how another country views us, at least our agriculture.

Going GM-free isn't the only agricultural change they're making. Others include:1
  • Stepping up supports for the Organic Farming Scheme for conversion to organic production.
  • Ensuring that new public procurement guidelines for food include criteria based on giving greater weight to sustainable local produce, seasonal menus and organic production.
  • Promoting and supporting a network of farmers' markets at Local Authority level to encourage more direct selling from producers to consumers.
Those are country-wide changes - a move that would lessen the kind of discrimination you see here in the US against those who do not have access to premium organic foods. Good for them.

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1 Proposed Renewed Programme for Government (pdf), 10th October 2009 (broken link)

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QUOTE
http://e360.yale.edu/content/print.msp?id=2228

Report

Behind Mass Die-Offs, Pesticides Lurk as Culprit

In the past dozen years, three new diseases have decimated populations of amphibians, honeybees, and — most recently — bats. Increasingly, scientists suspect that low-level exposure to pesticides could be contributing to this rash of epidemics.

by Sonia Shah
POSTED ON 07 Jan 2010 IN


Ever since Olga Owen Huckins shared the spectacle of a yard full of dead, DDT-poisoned birds with her friend Rachel Carson in 1958, scientists have been tracking the dramatic toll on wildlife of a planet awash in pesticides. Today, drips and puffs of pesticides surround us everywhere, contaminating 90 percent of the nation’s major rivers and streams, more than 80 percent of sampled fish, and one-third of the nation’s aquifers. According to the U.S. Fish and Wildlife Service, fish and birds that unsuspectingly expose themselves to this chemical soup die by the millions every year.

But as regulators grapple with the lethal dangers of pesticides, scientists are discovering that even seemingly benign, low-level exposures to pesticides can affect wild creatures in subtle, unexpected ways — and could even be contributing to a rash of new epidemics pushing species to the brink of extinction.

In the past dozen years, no fewer than three never-before-seen diseases have decimated populations of amphibians, bees, and — most recently — bats. A growing body of evidence indicates that pesticide exposure may be playing an important role in the decline of the first two species, and scientists are investigating whether such exposures may be involved in the deaths of more than 1 million bats in the northeastern United States over the past several years.

For decades, toxicologists have accrued a range of evidence showing that low-level pesticide exposure impairs immune function in wildlife, and have correlated this immune damage to outbreaks of disease. Consumption of pesticide-contaminated herring has been found to impair the immune function of captive seals, for example, and may have contributed to an outbreak of distemper that killed over 18,000 harbor seals along the northern European coast in 1988. Exposure to PCBs has been correlated with higher levels of roundworm infection in Arctic seagulls. The popular herbicide atrazine has been shown to make tadpoles more susceptible to parasitic worms.

The recent spate of widespread die-offs began in amphibians. Scientists discovered the culprit — an aquatic fungus called Batrachochytrium dendrobatidis, of a class of fungi called “chytrids” — in 1998. Its devastation, says amphibian expert Kevin Zippel, is “unlike anything we’ve seen since the extinction of the dinosaurs.” Over 1,800 species of amphibians currently face extinction.

It may be, as many experts believe, that the chytrid fungus is a novel pathogen, decimating species that have no armor against it, much as Europe’s smallpox and measles decimated Native Americans in the sixteenth and seventeenth centuries. But “there is a really good plausible story of chemicals affecting the immune system and making animals more susceptible,” as well, says San Francisco State University conservation biologist Carlos Davidson.

In California, for example, insecticides coated on the crops of the San Joaquin Valley are known to waft upwind to the Sierra Nevada mountains where they settle in the air, snow, and surface waters, and inside the tissues of amphibians. And when Davidson compared historical reports of pesticide use, habitat loss, wind patterns, and amphibian population counts in California for the years 1971 to 1991, he found a strong correlation between upwind pesticide use — in particular cholinesterase-inhibiting chemicals such as the insecticide carbaryl — and declining amphibian populations.

Experimental evidence bolsters Davidson’s findings. In lab experiments, exposure to carbaryl dramatically reduced yellow-legged frogs’ production of fungus-fighting compounds called antimicrobial peptides, which may be crucial to amphibians’ ability to fend off chytrid fungus. Further testing has shown that amphibian species that produce the most effective mixes of antimicrobial peptides resist experimental chytrid infection, and tend to be those that survive most successfully in the wild.

Six years after scientists discovered the fungal assault on amphibians, a mysterious plague began decimating honeybees. Foraging honeybees first started vanishing from their hives, abandoning their broods and queens to certain death by starvation, in 2004. Alarmed beekeepers dubbed the devastating malady “colony collapse disorder.” Between 2006 and 2009, colony collapse disorder and other ills destroyed 35 percent of the U.S. honeybee population.

Some experts believe colony collapse disorder is the result of a “perfect storm” of honeybee-debilitating factors: poor nutrition, immune dysfunction from decades of industrial beekeeping practices, and the opportunism of multiple pathogens, acting in malevolent concert. But many beekeepers believe that a new class of chemicals based on nicotine, called neonicotinoids, may be to blame.

Neonicotinoids came into wide use in the early 2000s. Unlike older pesticides that evaporate or disperse shortly after application, neonicotinoids are systemic poisons. Applied to the soil or doused on seeds, neonicotinoid insecticides incorporate themselves into the plant’s tissues, turning the plant itself into a tiny poison factory emitting toxin from its roots, leaves, stems, pollen, and nectar.

In Germany, France, Italy, and Slovenia, beekeepers’ concerns about neonicotinoids’ effect on bee colonies have resulted in a series of bans on the chemicals. In the United States, regulators have approved their use, despite the fact that the Environmental Protection Agency’s standard method of protecting bees from insecticides — by requiring farmers to refrain from applying them during blooming times when bees are most exposed — does little to protect bees from systemic pesticides.

“The companies believe this stuff is safe,” says U.S. Department of Agriculture (USDA) entomologist Jeff Pettis. “It is used at lower levels, and is a boon for farmers,” since neonicotinoids don’t require repeated application, nor wide broadcasting into the environment, he explains. Plus, years of research have shown that only very low levels of the chemicals are exuded from the pollen and nectar of treated plants.

But University of Padua entomologist Vincenzo Girolami believes he may have discovered an unexpected mechanism by which neonicotinoids — despite their novel mode of application — do in fact kill bees. In the spring, ’neonicotinoid-coated seeds are planted using seeding machines, which kick up clouds of insecticide into the air. “The cloud is 20 meters wide, sometimes 50 meters, and the machines go up and down and up and down,” he says. “Bees that cross the fields, making a trip every ten minutes, have a high probability of encountering this cloud. If they make a trip every five minutes, it is certain that they will encounter this cloud.”

And the result could be immediately devastating. In as-yet-unpublished research, Girolami has found concentrations of insecticide in clouds above seeding machines 1,000 times the dose lethal to bees. In the spring, when the seed machines are working, says Girolami, “I think that 90 percent or more of deaths of bees is due to direct pesticide poisoning.”

Girolami has also found lethal levels of neonicotinoids in other, unexpected — and usually untested — places, such as the drops of liquid that treated crops secrete along their leaf margins, which bees and other insects drink. (The scientific community has yet to weigh in on Girolami’s new, still-to-be-published research, but Pettis, who has heard of the work, calls it “a good and plausible explanation.”)

Two years after the honeybees started disappearing, so, too, did bats. The corpses of hibernating bats were first found blanketing caves in the northeastern United States in 2006. The disease that killed them, caused by a cold-loving fungus called Geomyces destructans — and dubbed White-nose Syndrome for the tell-tale white fuzz it leaves on bats’ ears and noses — has since destroyed at least one million bats. University of Florida wildlife ecologist John Hayes calls it “the most precipitous wildlife decline in the past century in North America.”

Like the mysterious Batrachochytrium dendrobatidis fungus infesting amphibians, Geomyces could be a novel pathogen, newly preying upon defenseless bat species. But scientists have also started to investigate whether pesticide exposure might be playing a role.

Bats are especially vulnerable to chemical pollution. They’re small — the little brown bat weighs just 8 grams — and can live for up to three decades. “That’s lots of time to accumulate pesticides and contaminants,” points out Boston University bat researcher and Ph.D. candidate Marianne Moore, who is studying whether environmental contaminants suppress bats’ immune function. “We know they are exposed to and accumulate organochlorines, mercury, arsenic, lead, dioxins,” she says, “but we don’t understand the effects.”

Which, in the end, is the central dilemma facing pesticide-reliant societies. Proving, with statistical certainty, that low-level pesticide exposure makes living things more vulnerable to disease is notoriously difficult. There are too many different pesticides, lurking in too many complex, poorly understood habitats to build definitively damning indictments. The evidence is subtle, suggestive. But with the rapid decimation of amphibians, bees, and bats, it is accumulating, fast.

POSTED ON 07 Jan 2010 IN
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believe_it
SICKENING (INTENTIONAL PUN)
QUOTE
http://www.lavidalocavore.org/diary/3059/g...dation-monsanto

Gates Foundation = Monsanto
by: Jill Richardson
Sat Jan 09, 2010 at 18:27:40 PM PST

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QUOTE
http://www.monsanto.com/monsanto_today/201...of_the_year.asp

Forbes Magazine Names Monsanto Company of the Year

January 4, 2010



On December 31, 2009, Forbes Magazine named Monsanto its Company of the Year for 2009. The magazine praised Monsanto's economic success and innovative new products.

Robert Langreth and Matthew Herper refered to the company as an economic winner in the Forbes article, "The Planet Versus Monsanto."

"It has created many billions of dollars of value for the world with seeds genetically engineered to ward off insects or make a crop immune to herbicides: Witness the vast numbers of farmers who prefer its seeds to competing products, and the resulting $44 billion market value of the company."

The Company of the Year recognition is a tribute to the company's valued employees and dedicated customers. Monsanto's success would not be possible without the hard-working farmers that continue to choose Monsanto's products over its competitors. "Farmers vote one spring at a time. You get invited back if you do a good job," said Hugh Grant, Monsanto’s president, chairman and CEO, in the Forbes article.

Read the full article: Forbes Magazine - The Planet versus Monsanto.

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Links from
http://www.democraticunderground.com/discu...ess=389x7435009
http://demopedia.democraticunderground.com...ess=389x7433744
believe_it
Link from http://viacampesina.org/main_en/

QUOTE


Under the spotlight

Welcome to the new international version of combat-monsanto.org. Now it’s easy for you to view our articles in English, Spanish and French. Our work is going global and citizens of the world can now see the true face of Monsanto.

Within these pages you will find alternative information about Monsanto and the firm’s products: GMO and Roundup, and also bovine growth hormone and Agent Orange.

In the “Protest” section you will find reports from many concerned NGOs and details of their activities. “A world of protest” keeps you informed on protests against Monsanto worldwide.

Finally “The Monsanto System” reveals the firm’s shady methods, describing how it infiltrates public bodies and how it puts scientists under pressure. It also provides a guide to decoding and understanding Monsanto’s propaganda aimed at the public...


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believe_it
QUOTE(believe_it @ Jan 10 2010, 07:04 PM) *
QUOTE
http://www.lavidalocavore.org/diary/3059/g...dation-monsanto

Gates Foundation = Monsanto
by: Jill Richardson
Sat Jan 09, 2010 at 18:27:40 PM PST

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Exploring the post above, I googled a name described as 'the boss' (Gates Foundation, President, Global Development Program) and found this impressive resume,
QUOTE
http://www.gatesfoundation.org/leadership/...ws-burwell.aspx

...Before joining the foundation, Burwell served in the Clinton administration as deputy director of the Office of Management and Budget, assistant to the president, deputy chief of staff to the president, and chief of staff to former Treasury Secretary Robert E. Rubin. Prior to her work in federal government, Burwell worked for McKinsey & Company, a management consulting firm, where she focused on consulting for financial institutions.

Burwell is a graduate of Harvard University and is a Rhodes scholar. She serves on the board of directors for MetLife Inc. and the Council on Foreign Relations and is a member of the board of the Alliance for a Green Revolution in Africa. Burwell is also a member of the Aspen Strategy Group, the Trilateral Commission and the Nike Foundation Advisory Group. She hails from Hinton, West Va.

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Do any of these individuals consume GMO foods themselves? And why is Gates associated with a surreal so-called Seed Vault as documented upthread (which, as described, was discovered accidentally while searching online for black lentils)?
believe_it
QUOTE
http://fanaticcook.blogspot.com/2010/01/ap...nst-use-of.html

Tuesday, January 12, 2010

APHA Issues Statement Against Use Of Hormones In Beef And Dairy Cattle

The American Public Health Association (APHA) came out against the use of exogenous hormones in general, and against one type of GMO in particular, in a recent statement:

Policy Statement: Opposition to the Use of Hormone Growth Promoters in Beef and Dairy Cattle Production, APHA, November 2009

Excerpts:
"There is clear evidence that hormones originating outside the body can interfere with our own hormone function."

"Many hormone-related chronic diseases are common or on the rise, including breast and prostate cancer, thyroid disease, obesity and diabetes, endometriosis, uterine fibroids, and infertility."

"Biological plausibility and scientific findings now suggest that exogenous hormones such as those used in our food system may be one such contributor to these negative trends."

"It is widely acknowledged that the use of these hormone growth promoters results in residues in meat."
In a 2007 study, for example, sperm concentration of male offspring was found to be inversely related to their mothers’ self-reported beef consumption while pregnant, with possible links hypothesized to the 6 steroid hormones routinely used in US beef production.1

It isn't just meat and dairy that may be problematic:
"Residues of these hormone growth promoters also persist for weeks to months in manure and feedlot runoff, raising concerns about the added exogenous hormone load to the environment."
The section on GMOs used in dairy cows (rbGH: recombinant bovine growth hormone) is particularly damning:
"Although some studies (including several funded by Monsanto) have failed to demonstrate that rbGH harms dairy cows, virtually all independent analyses of the data reached a different conclusion."
Canada, the European Union, Australia, New Zealand, and Japan have prohibited its use. Not the US:
"In 2007, nearly 43% of large herds were treated with rbGH."

Hormone Growth Promoters Just One of Many Environmental Endocrine Disruptors

The APHA Statement referenced and echoed the Endocrine Society's Statement from last summer (that I blogged about here):
"In its first scientific statement issued in June 2009, the Endocrine Society ... determined that 'Results from animal models, human clinical observations, and epidemiological studies converge to implicate EDCs [endocrine disrupting chemicals] as a significant concern to public health. ... Scientific knowledge about [EDCs’] effects on humans . . . appears sufficient to justify societal approaches to limiting population exposures.' "

Endocrine disruptors include hormones (GMO or conventional) fed to livestock as well as chemicals in plastics, pesticides, fuels, and cosmetics. EDs bioaccumulate in the food chain - they accrue in the fattier tissues of fish and other livestock. (In the future, a certification process may test animal products for ED concentrations.)

All of us have more of these chemicals in our bodies than did people just 50 years ago. Which leads me to the genetic issue...
believe_it
Aside: Post #203 emoticons not deliberate and were not present when initially posted.

Just found this heated thread at DU on Haiti relief which totally misses the points made by experts at OCA (below).
QUOTE
http://www.democraticunderground.com//disc...ess=389x7481389
This will be a big problem - the guy in overall charge of US Haiti relief has ONE WEEK of experience
Sat Jan-16-10 02:04 PM


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QUOTE(believe_it @ Nov 18 2009, 09:07 PM) *
Link from http://www.organicconsumers.org/ as, helpfully, are most links within the article, providing important backstory and context.
ESSENTIAL READING
QUOTE
http://capwiz.com/grassrootsnetroots/issue...lertid=14359511

Take Action: Stop Shah, Another of Obama's Biotech Boosters

Rajiv Shah, currently the USDA Under Secretary for Research, Education and Economics and Chief Scientist, has been nominated by President Obama to lead USAID.

Shah is on the board of directors for the Alliance for a Green Revolution in Africa (AGRA) and was the director of the Gates Foundation's Agriculture Development program. AGRA and the Gates Foundation have been criticized for working closely with Monsanto and its non-profit research arm, the Danforth Center. Links and collaborations include project partnerships, hiring one another's employees and making donations to one another's projects. At the Gates Foundation, Shah supervised Lawrence Kent, who had been the director of international programs at the Danforth Center and Monsanto vice president Robert Horsch, a scientist who led genetic engineering of plants at the seed giant.

In his short tenure at the USDA, he has used connections made at the Gates Foundation, which has distributed $37 million in grants for genetic engineering, to fill the USDA's Research, Education and Economics mission area with biotech scientists and advocates. These include Roger Beachy who directed Monsanto's Danforth Center, Maura O'Neill who ran a public-private venture dedicated to drawing biotech companies to the Seattle area where the Gates Foundation is based, and Rachel Goldfarb, another former Gates employee.

Shah has used his USDA post to champion genetic engineering and other novel technologies. In a report to Congress earlier this year on programs delivered by his mission area, Shah emphasized technology over ecology, saying, "We can build on tremendous recent scientific discoveries - incredible advances in sequencing plant and animal genomes, and the beginnings of being able to understand what those sequences actually mean. We have new and powerful tools in biotechnology and nanotechnology."

He has also directed millions of dollars toward GMO research. Shah has already awarded approximately $64 million in grants to improve crop characteristics through plant breeding, genetics and genomics.

These include $46 million through the Specialty Crop Research Initiative. (This money may not go exclusively to GMO research projects, but "science-based tools," "genetics and genomics," and "innovations and technologies," describe the initiative, while there is no mention of organic practices, conventional breeding or integrated pest management.)

Another $7 million goes to several universities for research to develop stress-resistant crops, a research topic that Monsanto promotes as their raison d'etre, despite the fact that they have never commericialized a single stress-resistant GMO plant, while hundreds of thousands of stress-resistant varieties are utilized by traditional farmers around the world who have saved seed and bred their plants conventionally for centuries.

The GMO research grants also include $11 million in Coordinated Agricultural Project grants to four research universities to study “plant genomics and ways to improve the nutrition and health values of important crops.” Expect more GMO tomatoes, potatoes, barley, soybean, and trees. And be on the lookout for new, GMO legumes embedded with cholesterol and diabetes drugs.

According to a USDA press release on the awards, “Because humans consume more legumes than any other crop, this research has the potential to reduce cholesterol and sugar levels, which in turn can prevent or alleviate certain types of cancer, type 2 diabetes and cardiovascular diseases.”

The irony is that there’s a GMO legume already on the market, soy, that has found its way into just about all processed and fried foods in the form of partially hydrogenated soybean oil (a.k.a. trans fat). Will the result of this research be a new GMO legume that treats diet-related diseases caused by other GMO legumes?

It would certainly be a first for the field of genetic engineering. In fact, any new GMO crop that actually improved the nutrition, health value, or stress-resistance of any crop would be a first. Contrary to popular belief, to date, there is not one consumer benefit associated with any GMO crop. They’re all genetically modified to either withstand or produce pesticides (usually manufactured by the chemical company that genetically engineered the crop).

The frightening thing is that the plan to create a genetically engineered legume that could reduce cholesterol and sugar levels would most likely be a pharma crop, a plant genetically engineered to produce a pharmaceutical. This is one of the most dangerous forms of genetic engineering. When grown outdoors on farmland, where most pharma crop trials have occurred, pharma crops can easily contaminate conventional and organic crops. In one chilling example from 2002, a corn crop engineered by ProdiGene to produce a vaccine for pigs contaminated 500,000 bushels of soybeans that were grown in the Nebraska field the next season. Before this incident, a similar thing had happened in Iowa where the USDA ordered ProdiGene to pay for the burning of 155 acres of conventional corn that may have cross-pollinated with some of the firm's biotech plants.

ProdiGene eventually went out of business, but not before it received a $6 million investment from the Governors Biotechnology Partnership, chaired by Iowa governor, Tom Vilsack, currently Shah's boss at the USDA. Vilsack didn't want any restrictions placed on experimental pharma crops. In reaction to suggestions that pharma crops should be kept away from food crops, Vilsack argued that "we should not overreact and hamstring this industry."

Roger Beachy, currently working under Shah as the USDA National Institute of Food and Agriculture director, joined Vilsack in support of ProdiGene and against regulation of pharma crops when he was still the director of Monsanto's research arm, the Danforth Center. He said in 2004 that scientists must be free to experiment in open fields:

"A ban would significantly halt the technology of producing drugs more cheaply in plants" than through current methods, Beachy said. And if work on biopharming to grow industrial chemicals were halted, "then you have stopped another kind of advance that we're looking for to give an economic advantage to our farmers."


In other news, the USDA announced on November 2, 2009, that an international team of scientists funded with a $10 million USDA grant has completed its first draft of the genome of a domesticated pig.

“Understanding the swine genome will lead to health advancements in the swine population and accelerate the development of vaccinations for pigs,” said Roger Beachy, NIFA director. “This new insight into the genetic makeup of the swine population can help reduce disease and enable medical advancements in both pigs and humans.”

And, it would aid Monsanto in their effort to patent pigs .

cutecat
Guest lineups for the today’s TV news shows:

ABC’s “This Week,” 9:30 a.m. — Guests: former President Bill Clinton; former President George W. Bush; Lt. Gen. Ken Keen, deputy commander of the U.S. Southern Command; Rajiv Shah, administrator of the U.S. Agency for International Development.

CBS’ “Face the Nation,” 11:30 a.m. — Guests: Clinton, Bush, Keen, Shah.

NBC’s “Meet the Press,” 9 a.m. — Guests: Clinton, Bush, Keen, Shah.

CNN’s “State of the Union,” 8 a.m. — Guests: Clinton; Bush; Keen; Shah; House Delegate Eleanor Holmes Norton, District of Columbia Democrat.

“Fox News Sunday,” 9 a.m. — Guests: Clinton; Bush; Keen; Shah; Sen. Mitch McConnell, Kentucky Republican.
believe_it
QUOTE
http://www.organicconsumers.org/articles/article_20042.cfm

An FDA Ban on Genetically-Engineered Milk is Twenty Years Overdue

Cancer Prevention Coalition, Jan 15, 2010

Straight to the Source: http://www.world-wire.com/news/1001150001.html

In May 2007, Samuel S. Epstein, MD, Chairman of the Cancer Prevention Coalition, and four other leading national experts on genetically-engineered, recombinant bovine growth hormone (rBGH) milk filed a Petition to the Food and Drug Administration (FDA), "Petition Seeking the Withdrawal of the New Animal Drug Application Approval for Posilac®-Recombinant Bovine Growth Hormone (rBGH)."

In the absence of any response, on January 12, 2010, Dr. Epstein resubmitted this Petition to Michael Taylor, Deputy Commissioner of the Food and Drug Administration.

As detailed in this Petition, Posilac® poses major public health hazards. Dr. Epstein requested his review and support of an early ban of Posilac®.

This Petitio requests the Secretary of Health and Human Services, and the Commissioner of Food and Drugs to suspend the approval of rBGH, a genetically engineered bovine growth hormone, and require milk and other dairy products produced with its use to be labeled with a warning such as, "Produced with the use of rBGH, and contains elevated levels of insulin-like growth factor, IGF-1, which poses major risks of breast, prostate, and colon cancers."

STATEMENT OF GROUNDS
  1. THE VETERINARY TOXICITY OF rBGH
    Evidence of these toxic effects was first detailed in confidential Monsanto reports, based on records of secret nationwide rBGH veterinary trials, submitted to the FDA prior to October 1989 when they were leaked to one of the petitioners, Dr. Epstein. He then made these reports available to Congressman John Conyers, Chairman of the House Committee on Government Operations. On May 8, 1990, Congressman Conyers issued the following statement, "I find it reprehensible that Monsanto and the FDA have chosen to suppress and manipulate animal health test data." Details of these toxic effects were subsequently admitted by Monsanto, and by the FDA, and were disclosed on the drug's veterinary label (Posilac®) in November, 1993. These toxic effects include injection site lesions, a wide range of other toxic effects, and an increased incidence of mastitis requiring the use and antibiotics, with resulting contamination of milk.

  2. ABNORMALITIES IN rBGH MILK
    A January 1994 Monsanto Executive Summary on rBGH, claimed that "natural milk is indistinguishable" from rBGH milk, and that "there is no legal basis requiring its labeling." However, there are a wide range of well-documented abnormalities in rBGH milk. These include: reduction in short-chain fatty acid and increase in long-chain fatty acid levels; increase in levels of a thyroid hormone enzyme; contamination with unapproved drugs for treating mastitis; and frequency of pus cells due to mastitis.

  3. INCREASED LEVELS OF INSULIN-LIKE GROWTH FACTOR 1 (IGF-1) IN rBGH MILK
    A wide range of publications have documented excess levels of IGF-1 in rBGH milk, with increases ranging from four- to 20-fold. Based on six unpublished industry studies, FDA admitted that IGF-1 levels in rBGH milk were consistently and statistically increased, and that these were further increased by pasteurization. These increases were also admitted by the pharmaceutical company Eli Lilly, in application for marketing authorization in the European Community. It should also be noted that pasteurization of milk increases IGF-1 levels.

  4. IGF-1 IS READILY ABSORBED FROM THE INTESTINE INTO THE BLOOD
    IGF-1 is a small protein component known as a peptide. As such it is readily absorbed into the blood. It survives digestion, and has marked growth promoting effects following short-term feeding tests in rats.

  5. INCREASED IGF-1 LEVELS IN MILK INCREASE RISKS OF BREAST, COLON AND PROSTATE CANCERS
    Increased levels of IGF-1 have been shown to increase risks of breast cancer in 19 scientific publications, risks of colon cancer in 10 publications, and prostate cancer in 7 publications.

  6. INCREASED IGF-1 LEVELS INHIBIT "APOPTOSIS"
    Of critical importance is the fact that increased IGF-1 levels block natural defense mechanisms, known as apoptosis, against early submicroscopic cancers.

  7. rBGH INCREASES TWINNING RATES
    An increased rate of twinning in cows injected with rBGH was admitted by Monsanto on its November 1993 Posilac® label, and the incidence of fraternal twins. Monsanto also admitted that it increases "and complications such as premature delivery, congenital defects and pregnancy-induced hypertension."

  8. THE INTERNATIONAL BAN ON THE USE AND IMPORTS OF U.S. rBGH DAIRY PRODUCTS
    Based on well-documented veterinary and public health concerns, in June 30, 1999, the United Nations Food Safety Agency, representing 101 nations worldwide, ruled unanimously not to endorse or set a safety standard for rBGH milk. Effectively, this has resulted in an international ban on U.S. milk, approximately 20% of which is rBGH.

  9. FDA POLICY ON LABELING rBGH MILK
    The FDA continues to mislead dairy producers and consumers with regard to its requirement for labeling of rBGH milk, with its deliberately false claim that "No significant difference has been shown between milk derived from rBST-treated and non-rBST treated cows." "In fact," warns Dr. Epstein, "rBGH milk continues to pose major cancer and other risks to the entire U.S. population."
The 2007 Petition has been endorsed by four other leading experts on genetically-engineered, recombinant bovine growth hormone (rBGH) milk. We look forward to a response.

Samuel S. Epstein, M.D.
Professor emeritus Environmental and Occupational Health
University of Illinois School of Public Health
Chairman, Cancer Prevention Coalition
Chicago, IL

Email: epstein@uic.edu
Web: http://www.preventcancer.com

Ronnie Cummins
National Director
Organic Consumers Association
Finland, MN

Email: ronnie@organicconsumers.org
Web: http://www.organicconsumers.org

John Kinsman
President
Family Farm Defenders
Madison, WI

Email: jepeck@students.wisc.edu
Web: http://www.www.familyfarmdefenders.org

Arpad Pusztai, PhD, FRSE
Consultant Biologist
Scotland

Email: a.pusztai@freenet.co.uk

Jeffrey Smith
Executive Director
Institute for Responsible Technology
Fairfield, IA

Email: jeffrey@seedsofdeception.com
Web: http://www.seedsofdeception.com

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believe_it
FROM SUPERMARKET NEWS
QUOTE
http://supermarketnews.com/viewpoints/stak...1207/index.html

Stakeholders in GMO Debate Prepare to Clash Again

Stakeholders in GMO Debate Prepare to Clash Again

Dec 7, 2009 12:00 PM, By ROBERT VOSBURGH

In the food industry, there are always culprits. They usually have long tenures, and can even define the decade in which they were topical. In the '80s, it was fat; in the '90s, it was carbs. So far, as we near the end of the first decade of a new century, it would seem to be a toss-up between sodium and added sugar. We still have a year left to determine which one claims the title.

There are other issues that grab consumer interest but, for whatever reason, never seem to break through the public consciousness and out into the open. This has been the case with genetically modified foods.

Government statistics from 2007 show that the vast majority of the country's commodity ingredients come from GMO crops: 91% of soy, 87% of cotton and 73% of corn. It's estimated that GMOs are now present in more than 80% of packaged food products found in U.S. or Canadian supermarkets.

The coming year promises to bring about a greater, more pervasive awareness of those numbers as opponents of GMOs bring a unified campaign — complete with a non-GMO standard — to the public.

The Non-GMO Project has launched the country's first consensus-based guidelines, which include third-party certification and a uniform seal for approved products. Tests must indicate that the ingredient is below 0.9% GMO — compatible with laws in the European Union. The organization also requires documented traceability and segregation to ensure the tested ingredients are what go into the final product.

Concurrent with this, a new non-GMO website was launched by the Institute for Responsible Technology that provides consumers with a directory of non-GMO brands. The site was developed “for the 53% of Americans who say they would avoid GMOs if labeled.”

The website and the label have the potential to spark a new round of concern among shoppers who are today much more attuned to the ways their food is produced. The growth of the organic (which bans GMO ingredients), local and green product categories reflects a generation of consumers who could be less tolerant of genetic modification.

Yet, this whole issue might still go away (again), if the concept of GMOs is changed. A study written up in a recent New York Times blog noted that when apples from the Midwest, modified to resist apple scab disease, were presented to local consumers labeled “Reduced Environmental Impact,” they scored much higher on the preference scale. The test subjects liked that the apples required fewer pesticides and fungicides, and were locally grown.

The study raises an interesting question: Is genetic modification a problem of science, or of marketing? Ultimately, that's the question to answer: Not whether GMO foods are bad, in and of themselves; rather, does the technology allow us to reduce or eliminate older, more obvious evils?

Respond to SN's Viewpoints online atsupermarketnews.com

QUOTE
http://www.huffingtonpost.com/jeffrey-smit...e_b_416861.html

'Supermarket News' Forecasts Non-GMO Uprising

by Jeffrey M Smith
Posted: January 8, 2010 05:26 PM


For a couple of years, the Institute for Responsible Technology has predicted that the US would soon experience a tipping point of consumer rejection against genetically modified foods; a change we're all helping to bring about. Now a December article in Supermarket News supports both our prediction and the role the Institute is playing.

"The coming year promises to bring about a greater, more pervasive awarenes" of the genetically modified organisms (GMOs) in our food supply, wrote Group Editor Robert Vosburgh, in a trade publication that conventional food executives and retailers use as a primary source of news and trends in the industry. Vosburgh describes how previous food "culprits" like fat and carbs "can even define the decade in which they were topical," and suggests that GMOs may finally burst through into the public awareness and join their ranks.

Vosburgh credits two recent launches with "the potential to spark a new round of concern among shoppers who are today much more attuned to the ways their food is produced." One is our Institute's new non-GMO website, which, he says, "provides consumers with a directory of non-GMO brands . . . developed ‘for the 53% of Americans who say they would avoid GMOs if labeled.'"

The other launch is the Non-GMO Project, offering "the country's first consensus-based guidelines, which include third-party certification and a uniform seal for approved products. . . . The organization also requires documented traceability and segregation to ensure the tested ingredients are what go into the final product."

He alerts supermarket executives that, "the growth of the organic (which bans GMO ingredients), local and green product categories reflects a generation of consumers who could be less tolerant of genetic modification."

Please allow me to sit back with an I-told-you-so grin of satisfaction. Two years ago, I wrote a newsletter article describing three components that would move the market on GMOs:

1. The Non-GMO Project's new "widely accepted definition for non-GMO" would spark a GMO cleanout, starting with the brands in the natural food industry.
Our Institute endorses the Non-GMO Project and encourages food companies to enroll their products with this excellent nonprofit organization. Their official seal was introduced in October 2009 and has quickly become the national standard for meaningful non-GMO claims.

2. "Providing clear Non-GMO product choices" with our Non-GMO Shopping Guide would make it easier for consumers to select "non-GMO products by brand and category."
The same Guide is available as a website, a spread in magazines, a pocket guide, a two-sided download, and coming soon, a mobile phone application.

3. "Educating Health-Conscious Shoppers" about the health effects of GMOs is the key means by which GMOs will become a marketing liability—the next culprit.
Past culprits drove the market because of consumer beliefs that were unhealthy. In the same way, evidence demonstrating the health dangers of GMOs is already igniting an anti-GMO fever. In 2009, for example, the prestigious American Academy of Environmental Medicine urged doctors to prescribe non-GMO diets for all patients, based on evidence that GMOs fed to lab animals triggered diseases and disorders.

GMO Rejection Will Be Widespread

The prognosis in Supermarket News overlooks critical differences between GMOs and the other culprits. Fats, carbs, salt, and sugar each offer unmistakable consumer appeal. As a result, food companies offer options with them, without them, and at low levels.

Genetically modified (GM) foods, however, don't offer a single consumer benefit. The five major GMOs—soy, corn, cottonseed, canola, and sugar beets—are gene-spliced to either tolerate poisonous herbicides, or produce poisonous insecticides. Consumers never clamor for them.

Also unlike the other culprits, companies can usually eliminate GMOs without even changing recipes. Purchasers can simply instruct suppliers to provide the non-GMO soy and corn derivatives, the non-GMO sugar, etc., as Trader Joe's and Whole Foods have already done for their home brands.

Therefore, when major food companies notice even tiny losses in market share, their GMO cleanout will be widespread. Kraft Foods and others will recognize that the same consumer trend that forced them to remove all GM ingredients in Europe and Japan has reared its head in the States.

Consumer Opinion Already Poised Against Biotech Food

We're already seeing the momentum build against genetically engineered bovine growth hormone. Wal-Mart, Starbucks, Dannon, Yoplait, and most dairies have shunned the controversial drug that is now synonymous with "increased cancer risk" in the minds of many consumers. (The recent condemnation of the hormone by the American Public Health Association will help nail its coffin shut.)

In the case of GMOs, the proportion of US consumers needed to avoid brands that contain GM soy and corn, etc. is quite small—probably only 5%. That means that the purchasing power (and trend setting ability) of 15 million people or 5.6 million households can turn GMOs into a marketing liability. But when you look at the numbers, no matter how you slice it, they add up to a coming non-GMO tidal wave.

About 28 million health-conscious Americans regularly buy organic. About 87 million are strongly opposed to GM foods and believe they are unsafe. And 159 million say they would avoid GMOs if labeled. While most people do not conscientiously avoid brands with GM ingredients, its usually because they don't know how. That's where our Non-GMO Shopping Guide comes in—disseminated far and wide in 2010.

Vosburgh says that in the food industry, culprits "can even define the decade in which they were topical. In the '80s, it was fat; in the '90s, it was carbs." We won't need a full decade to send GMOs packing. Although I can't forecast the exact timing, I'll wager one prediction. By this time next year, Monsanto—the largest GMO producer—is not going to be happy.

International bestselling author and filmmaker Jeffrey M. Smith is the executive director of the Institute for Responsible Technology and the leading spokesperson on the health dangers of GMOs. His first book, Seeds of Deception, is the world's bestselling and #1 rated book on the subject. His second, Genetic Roulette, documents 65 health risks of the GM foods Americans eat everyday.


Follow Jeffrey Smith on Twitter: http://twitter.com/JeffreyMSmith
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As described earlier on this thread, I discovered the extraordinary autism blog, http://adventuresinautism.blogspot.com/ ,via a Yahoo search on genetically modified food which popped up a link to one of these outstanding posts - (search results link from Ginger Taylor's blog does not transfer; enter 'GMO' into site's excellent search engine)

after I discovered the issue of GMO from the censored online documentary (now widely available), THE WORLD ACCORDING TO MONSANTO, from a link probably at DU. Then one day my mouse inadvertently opened a link from Ginger Taylor's website to the 2008 awards at http://ageofautism.com . To say I've been shocked by all this is understatement.

Here's a crossover post which could be added legitimately to either the autism or GMO thread. This crisis belongs to all of us, by the way. Ignoring it won't work.

QUOTE
http://www.ageofautism.com/2010/01/autism-...ption.html#more

January 25, 2010

Autism Father to Chicago Tribune: "Cancel My Subscription."

By Sym and Wade Rankin

My wife and I subscribed to the Chicago Tribune soon after moving into the area a little over three years ago. Recent articles led us to the conclusion that their editorial bias hindered, rather than aided a productive debate on the most important issue in our household: our response to the growing autism epidemic. We therefore took that most American of steps; we cancelled our subscription and made sure the paper knew why we did so. Here's the letter:
Mr. Tony Hunter
President, Publisher
Chicago Tribune Company
435 North Michigan Avenue
Chicago, IL 60611

Dear Mr. Hunter:

A few days ago, we called the circulation department to cancel our subscription to The Chicago Tribune. We thought it appropriate to write and explain why we thought this necessary. Put briefly, the Tribune’s continuing written assault on the autism community and those who serve us has caused us to lose the high degree of respect we once held for your newspaper.

Specifically, articles written (or co-written) by Trine Tsouderos have, in our opinion, strayed from the principles of balance, fairness, and the truth.

By way of background explanation, our family is one of the hundreds of thousands in this country who have felt the impact of the autism epidemic.

We are part of a growing number of people who have chosen not to meekly embrace our son’s disability, but rather to seek biological explanations for the clinical manifestations that led to the diagnosis and to utilize the best medical treatments to treat the underlying physical conditions. We are not alone on this journey, and like most of the parents who embark on this course, we are well-educated. Both of us have professional backgrounds (including a background in mainstream medicine).

Each case of autistic spectrum disorder is unique from a standpoint of both cause and treatment. We have utilized some so-called “alternative” therapies together with more traditional treatments. The continued improvement of our son’s clinical manifestations has been nothing short of remarkable. Our story is not unique; there are many of us who have seen first-hand the success that can result from treating underlying physical conditions instead of just the symptoms by which autism traditionally has been defined.

Many in our community have attempted to speak to Ms. Tsouderos about the healing we have seen in our children, but she has shown little interest in exploring our perspectives. Instead, she chooses to rely on the same talking points we have so often heard from groups and individuals with vested interests, while ignoring scientific studies providing a basis for the treatments.. On those occasions when she does quote someone – whether a parent, a practitioner or a scientist – that quote is invariably taken out of context and is either inaccurate or incomplete. For example, an article this past November, mined several quotes from Dr. Martha Herbert, a distinguished neurologist at Harvard. This was Dr. Herbert’s response to the Tribune, which your paper chose to ignore:

"I did a rather long interview with the Tribune to explain my thoughts on chelation and additional approaches to solving the health issues connected to autism. The only consequence of my interview is that you use a solitary quote to make me sound contentious and defensive. Is there a reason you chose not to use something I said that would actually illuminate the discussion surrounding chelation and other medical treatments for medical compromises that may exist in these children?"
To be sure, this is a complex and often controversial subject. The Tribune’s editorial stance on autism treatments, however, seems inconsistent with other positions it has taken. Recently, your paper printed an exposé on overuse of drugs at nursing homes, a worthwhile subject. Why is the only focus of your autism coverage upon so-called “alternative” treatments? Why is no attention paid to the frighteningly large number of physicians who want to treat autistic children under the age of five with dangerous stimulants and psychiatric pharmaceuticals? And why does the Tribune not show outrage at the fact that the American Academy of Pediatrics endorses that off-label usage of pharmaceuticals in their published treatment recommendations for autism?

The Tribune has run recent articles on rising numbers of allergies (including one noting the difficulties the Army is having in filling its ranks due to high incidences of allergies and asthma). Is your paper at all interested in exploring the interrelationship in the alarming rise of various auto-immune disorders: childhood cancer, asthma, allergies, ADHD and autism spectrum disorders (although not unanimous, more and more scientists are acknowledging that disorders in the immune system can cause clinical manifestations of autism)?

Our kids are the canaries in the coal mine. Something is going wrong with an entire generation, and it is rooted in environmental causes: adulteration of our food supply, chemical pollution, contamination of our water, overuse of antibiotics, and quite possibly a public vaccination schedule gone haywire.

It’s not just scientific research that’s needed to put these puzzle pieces together; we also need the illumination of the questions in order to solving the questions a public priority. The role of the press is to present the issues in such a manner as to fairly raise the questions. In that, the Tribune has fallen well short of its duty.

The articles by Ms. Tsouderos were given front-page treatment, including the latest, which came at a time when every other organ of the press was focused squarely on the recent tragedy in Haiti. The lack of proportionality in that is summed up in one question. Why did the Tribune not show equal alarm with a major front-page article last month, when the Centers for Disease Control announced new autism statistics? According to the CDC, autism spectrum disorders effect one-in-110 children (one-in–every-seventy boys), which is a dramatic increase from the one-in 150 the CDC announced just two years ago.

This country is facing a public-health crisis of catastrophic proportions, in which too many families are having to make difficult decisions. Instead of amplifying the seriousness of the situation, the Tribune has chosen to blindly criticize some of the scientists and clinicians who are searching for the answers.

We have no doubt that the loss of our subscription will have little economic impact on your company. Further, the publication of the articles in question will have little adverse impact on the Tribune’s reputation – at least not immediately. What the Tribune has lost, however, is far more precious. It has lost the integrity upon which the paper’s reputation was built through generations.

Yours truly,

Sym and Wade Rankin

cc: Samuel Zell
Chairman, Tribune Company
Wade Rankin and his wife, Sym, are the proud parents of a 10-year-old son, who is well on the way to recovery. His on-again/off-again blog is called Injecting Sense.

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On today's OCA homepage,

QUOTE
http://www.organicconsumers.org/articles/article_18377.cfm

Monsanto & Dole Team Up to Force-Feed Consumers Genetically Engineered Fruits & Veggies
Dole, Monsanto enter into innovation agreement

By Eric Schroeder
Food Business News, June 23, 2009


MONTEREY, CALIF. - Dole Fresh Vegetables, Inc. and Monsanto Co. have entered into an agreement to develop new products that will "enhance consumer vegetable choices," according to the companies. The five-year agreement will focus on broccoli, cauliflower, lettuce and spinach. Any new products developed through the agreement will be commercialized by Dole in North America.

Plant breeding techniques will be used to improve the nutrition, flavor, color, texture, taste and aroma of the vegetables. Monsanto's role in the collaboration will be to improve the development of new and beneficial vegetable characteristics. Their efforts will be guided by Dole's knowledge of consumer needs and marketing.

"Dole prides itself on innovation and bringing consumers high quality, nutritious and great-tasting products," said Roger Billingsley, senior vice-president of research and development for Dole Fresh Vegetables. "We are looking forward to collaborating closely with Monsanto to do just that."


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Link today about '05 Monsanto article (oddly) with 65 OUTRAGED comments from: http://www.democraticunderground.com/discu...ess=389x7621991

QUOTE
http://www.seedalliance.org/Seed_News/SeminisMonsanto/

Monsanto Purchases World’s Largest Vegetable Seed Company

“Monsanto Company to Acquire Seminis, Inc., a Leading Vegetable and Fruit Seed Company
Acquisition Expected to Add Near-term Income Growth and Diversity to Monsanto's Seed Portfolio

ST. LOUIS (Jan. 24, 2005)
Monsanto Company (NYSE: MON) announced today that it signed a definitive agreement to acquire Seminis, Inc., for $1.4 billion in cash and assumed debt…

The news of Monsanto’s agreement to purchase Seminis has received little attention from the media other than the financial pages and a few seed industry and anti-globalization web sites. But then again, why should it? How many consumers – of food or seed – have even heard of Seminis? And yet, as Seminis spinmeister Gary Koppenjan said, “If you've had a salad, you've had a Seminis product."

It is estimated that Seminis controls 40 percent of the U.S. vegetable seed market and 20 percent of the world market—supplying the genetics for 55 percent of the lettuce on U.S. supermarket shelves, 75 percent of the tomatoes, and 85 percent of the peppers, with strong holdings in beans, cucumbers, squash, melons, broccoli, cabbage, spinach and peas. The company’s biggest revenue source comes from tomato and peppers seeds, followed by cucumbers and beans...

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QUOTE
http://www.huffingtonpost.com/jeffrey-smit...g_b_436384.html

Rude Awakening

by Jeffrey Smith
Posted: January 25, 2010 11:36 PM

A wise customer wanted to find out if the corn nuts she was eating were from genetically modified (GM) corn. She emailed the company and got a shocking reply. It began:
"Thank you for your contact. We are not aware of any GMO free corn in the U.S. We feel it is a ridiculous concern based on very poor science."
The email, reproduced at the blog of Kelly the Kitchen Kop , even recommended:
". . . if these concerns are truly important to you, you may be better served at a health food store.
We appreciate your patronage.
The Customer Support Team,
American Importing Co., Inc."
Talk about being opinionated and misinformed.

There's overwhelming evidence showing that genetically modified organisms (GMOs) are unsafe. And there are plenty of sources for non-GMO corn.

See (available only on cache view):
http://74.125.95.132/search?q=cache:fqsMc0...=clnk&gl=us



Did this email get you angry? Are you thinking about flooding the company's email with hostile missives? I had another idea.

I phoned the company owner.

I figured that although the email's author was clearly misled, I also knew all about Monsanto and the other devious corporations that dis-informed him—and how they skillfully depict GMO critics as ridiculous and unscientific.

When I got President Andy on the phone and asked if his products were genetically modified (GM), it didn't take me long to realize that he was almost certainly the author of his company's tactless email. He launched into a diatribe blasting GMOs as the most misconceived issue in the entire food industry.

As I took notes documenting his string of incorrect statements, (no, there is no GMO wheat yet, same with apples; no there was not a massive death of monarch butterflies in Europe), he heard my keyboard tapping and stopped momentarily to ask who I was. I told him that I was a leading spokesperson on the dangers of GMOs, that I wrote the world's bestselling book on the subject , and that I was doing a blog based on an email response sent by his customer service.

That didn't slow him down in the least. Andy continued his rant, which literally went on for 12 minutes. I was impressed.

When he finally ran out of steam, I decided to begin my response by agreeing with him—that we certainly do need to apply real science on this issue. Then I told him the truth.

I told Andy of concerns by FDA scientists that GMOs might create serious, hard-to-detect health hazards, and how Monsanto's man placed at the top of the agency ignored and covered-up the warnings. As a result, the FDA lets GMOs onto the market without any required safety tests.

I told Andy that I worked with more than 30 scientists to document 65 health risks of GMOs for my book Genetic Roulette , which cites peer-reviewed science, industry research, and medical investigations, among its 1100+ endnotes.

I told Andy about the American Academy of Environmental Medicine's condemnation of GMOs, and their prescription of non-GMO diets for all patients. And how this renowned physician's organization linked GMOs to infertility, immune system dysfunction, gastrointestinal problems, organ damage, and disruption of insulin and cholesterol regulation.

And I told Andy how the same corporations that fed him the lie that GMOs are safe, fired and gagged scientists who discovered that they're not.

Now Andy was impressed.

And he realized he had been duped—that the information given to him and others in the food industry had been "filtered" by those earning profits from GMOs. He said that the science that I presented was not getting to the executives in the food industry, to people like him who want to give customers healthy food.

Andy was again on a roll, but with a different agenda. He now urged me to get in front of the decision makers in the food industry, and he even offered to help make it happen.

I told Andy that I was impressed by his passion, which he had unleashed on me like a fire hose at the beginning of the call. And I knew that once armed with the real evidence against GMOs, he could use that same passion and make a big difference.

Andy committed to order and read Genetic Roulette: The Documented Health Risks of Genetically Engineered Foods. And while waiting for it to arrive, he and his colleagues will review my keynote speech online, Everything You HAVE TO KNOW About Dangerous Genetically Modified Foods .

Before we hung up, Andy thanked me over and over for not being reactive to his initial onslaught, and for staying with him and leading him through the science.

I now have a new friend. And I am reminded again about the importance of educating leaders in the food industry as part of our campaign to rid the food supply of GMOs.

If you know a food company executive, please take the time to send him or her a link to the online video presentation, to the article showing that doctors now prescribe non-GMO diets, and to a summary of the GMO health risks. It's time well spent.

And if they run a very large food company, please introduce me. I'm on a roll.

Safe eating.


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QUOTE
http://www.huffingtonpost.com/jeffrey-smit...e_b_319998.html

Vilsack Mistakenly Pitched "GMOs-Feed-The-World" to an Audience of Experts - Oops

by Jeffrey Smith
Posted: October 13, 2009 11:22 PM


Agriculture Secretary Tom Vilsack was getting lots of appreciative applause and head nods from the packed hall at the Community Food Security Coalition conference today, held in Des Moines, Iowa. He described the USDA's plans to improve school nutrition, support local food systems, and work with the Justice Department to review the impact of corporate agribusiness on small farmers. But then, with time for only one more question, I was handed the microphone.
"Mr. Secretary, may I ask a tough question on GMOs?"
He said yes.
"The American Academy of Environmental Medicine this year said that genetically modified foods, according to animal studies, are causally linked to accelerated aging, dysfunctional immune regulation, organ damage, gastrointestinal distress, and immune system damage. A study came out by the Union of Concerned Scientists confirming what we all know, that genetically modified crops, on average, reduce yield. A USDA report from 2006 showed that farmers don't actually increase income from GMOs, but many actually lose income. And for the last several years, the United States has been forced to spend $3-$5 billion per year to prop up the prices of the GM crops no one wants.

"When you were appointed Secretary of Agriculture, many of our mutual friends--I live in Iowa and was proud to have you as our governor--assured me that you have an open mind and are very reasonable and forward thinking. And so I was very excited that you had taken this position as Secretary of Agriculture. And I'm wondering, have you ever heard this information? Where do you get your information about GMOs? And are you willing to take a delegation in D.C. to give you this hard evidence about how GMOs have actually failed us, that they've been put onto the market long before the science is ready, and it's time to put it back into the laboratory until they've done their homework."

The room erupted into the loudest applause of the morning.

Secretary Vilsack knew at once what kind of crowd he was dealing with. Or so I thought.

He said he was willing to visit with folks, to read studies, to learn as much as he possibly can. He pointed out that there are lots of studies, not necessarily consistent, even conflicting. He said he was in the process of working on a set of regulations and had brought proponents and opponents together to search for common ground. And he was looking to create a regulatory system with sufficient assurances and protections.

At this point in his answer, Secretary Vilsack, who has a history of favoring GMOs--and even appears to be more pro-GMO than his Bush administration predecessors--was trying to sound even handed. Then he made a tragic mistake.

After a slight pause, he added in a warm tone, "I will tell you that the world is very concerned about the ever-increasing population of the globe and the capacity to be able to feed all of those people."

Moans, groans, hisses, even boos. Not rowdy, mind you. But clearly agitated.

You see, the people in the room were among the top experts at actually feeding the world. They included numerous PhDs who had spent their careers looking deeply into the issue. Among those present were several of the authors of the authoritative IAASTD report . The International Assessment of Agricultural Knowledge, Science and Technology for Development, is the most comprehensive evaluation of world agriculture ever. It was a three-year collaborative effort with 900 participants and 110 countries, and was co-sponsored by all the majors, e.g. the World Bank, FAO, UNESCO, WHO. The behemoth effort evaluated the last 50 years of agriculture, and prescribed the methods that were now needed to meet the development and sustainability goals of reducing hunger and poverty, improving nutrition, health and rural livelihoods, and facilitating social and environmental sustainability.

And GMOs was not one of those needed methods! It was clear to the experts that the current generation of GMOs did not live up to the hype continuously broadcast by biotech companies and their promotional East Coast wing--the federal government.

In fact, the night before Vilsack addressed the conference, the same audience heard a keynote by Hans Herren, the co-chairman of the IAASTD report, during which he reiterated that biotechnology was not up to the task. And this morning, Hans Herren was in the room when Vilsack tried to play the feed-the-world card. Bad move.

Vilsack responded to the crowd's rejection by saying, "And well you all can disagree with this, but I am just telling you this. As I travel the world, I am just telling you what people are telling me. They are very concerned about this."

Thus, he distanced himself from the contentious, and fallacious, argument. He was just reporting what others had told him.

And that may in fact be his problem with understanding the serious health and environmental dangers of GMOs in general, if he is simply, as he says, repeating what others--Monsanto, Syngenta, DuPont--have told him over and over again.

It's true that I have mutual friends of Tom Vilsack who like and respect him and believe him to be reasonable and thoughtful. I have seen this myself, but not on the GMO issue.

Perhaps the reaction of the experts this morning will help to jar him out of his GMOs-feed-the-world mindset. Unfortunately, he is now deeply immersed in the second of this week's food conferences here in Des Moines, the World Food Prize. It features the major GMO promoters from around the world, including Bill Gates (who gives tens of millions to GMO development in Africa), and top executives of DuPont and Syngenta. Expect to hear constant chatter about how GMOs are the solution to world hunger which, unfortunately, may undue any of the restructuring that this morning's run-in with reality may have awakened.

In the meantime, if there are Q & A sessions at meetings where Secretary Vilsack is speaking or attending, I'll do my best to get to a mic.


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MUST READ
QUOTE
http://www.seedsofdeception.com/utility/sh.../?objectID=1479

EXCERPT Spilling the Beans, October 2007

The FDA’s “non-regulation” of GM foods

Genetically modified crops are the result of a technology developed in the 1970s that allow genes from one species to be forced into the DNA of unrelated species. The inserted genes produce proteins that confer traits in the new plant, such as herbicide tolerance or pesticide production. The process of creating the GM crop can produce all sorts of side effects, and the plants contain proteins that have never before been in the food supply. In the US, new types of food substances are normally classified as food additives, which must undergo extensive testing, including long-term animal feeding studies.[4] If approved, the label of food products containing the additive must list it as an ingredient.

There is an exception, however, for substances that are deemed “generally recognized as safe” (GRAS). GRAS status allows a product to be commercialized without any additional testing. According to US law, to be considered GRAS the substance must be the subject of a substantial amount of peer-reviewed published studies (or equivalent) and there must be overwhelming consensus among the scientific community that the product is safe. GM foods had neither. Nonetheless, in a precedent-setting move that some experts contend was illegal, in 1992 the FDA declared that GM crops are GRAS as long as their producers say they are. Thus, the FDA does not require any safety evaluations or labels whatsoever. A company can even introduce a GM food to the market without telling the agency.

Such a lenient approach to GM crops was largely the result of Monsanto’s legendary influence over the US government. According to the New York Times, “What Monsanto wished for from Washington, Monsanto and, by extension, the biotechnology industry got. . . . When the company abruptly decided that it needed to throw off the regulations and speed its foods to market, the White House quickly ushered through an unusually generous policy of self-policing.” According to Dr. Henry Miller, who had a leading role in biotechnology issues at the FDA from 1979 to 1994, “In this area, the U.S. government agencies have done exactly what big agribusiness has asked them to do and told them to do.”

Following Monsanto’s lead, in 1992 the Council on Competitiveness chaired by Vice President Dan Quayle identified GM crops as an industry that could increase US exports. On May 26, Quayle announced “reforms” to “speed up and simplify the process of bringing” GM products to market without “being hampered by unnecessary regulation.”[5] Three days later, the FDA policy on non-regulation was unveiled.

The person who oversaw its development was the FDA’s Deputy Commissioner for Policy, Michael Taylor, whose position had been created especially for him in 1991. Prior to that, Taylor was an outside attorney for both Monsanto and the Food Biotechnology Council. After working at the FDA, he became Monsanto’s vice president.

Covering up health dangers

The policy he oversaw needed to create the impression that unintended effects from GM crops were not an issue. Otherwise their GRAS status would be undermined. But internal memos made public from a lawsuit showed that the overwhelming consensus among the agency scientists was that GM crops can have unpredictable, hard-to-detect side effects. Various departments and experts spelled these out in detail, listing allergies, toxins, nutritional effects, and new diseases as potential problems. They had urged superiors to require long-term safety studies.[6] In spite of the warnings, according to public interest attorney Steven Druker who studied the FDA’s internal files, “References to the unintended negative effects of bioengineering were progressively deleted from drafts of the policy statement (over the protests of agency scientists).”[7]

FDA microbiologist Louis Pribyl wrote about the policy, “What has happened to the scientific elements of this document? Without a sound scientific base to rest on, this becomes a broad, general, ‘What do I have to do to avoid trouble’-type document. . . . It will look like and probably be just a political document. . . . It reads very pro-industry, especially in the area of unintended effects.”[8]

The FDA scientists’ concerns were not only ignored, their very existence was denied. Consider the private memo summarizing opinions at the FDA, which stated, “The processes of genetic engineering and traditional breeding are different and according to the technical experts in the agency, they lead to different risks.”[9] Contrast that with the official policy statement: “The agency is not aware of any information showing that foods derived by these new methods differ from other foods in any meaningful or uniform way.”[10] On the basis of this manufactured and false notion of no meaningful differences, the FDA does not require GM food safety testing.

To further justify their lack of oversight, they claimed that GM crops were “substantially equivalent” to their natural counterparts. But this concept does not hold up to scrutiny. The Royal Society of Canada described substantial equivalence as “scientifically unjustifiable and inconsistent with precautionary regulation of the technology.” In sharp contrast to the FDA’s position, the Royal Society of Canada said that “the default prediction” for GM crops would include “a range of collateral changes in expression of other genes, changes in the pattern of proteins produced and/or changes in metabolic activities.”[11]

Fake safety assessments

Biotech companies do participate in a voluntary consultation process with the FDA, but it is derided by critics as a meaningless exercise. Companies can submit whatever information they choose, and the FDA does not conduct or commission any studies of their own. Former EPA scientist Doug Gurian-Sherman, who analyzed FDA review records obtained through the Freedom of Information Act, states flatly, “It is clear that FDA’s current voluntary notification process (even if made mandatory) is not up to the task of ensuring the safety of future GE [genetically engineered] crops.” He says, “The FDA consultation process does not allow the agency to require submission of data, misses obvious errors in company-submitted data summaries, provides insufficient testing guidance, and does not require sufficiently detailed data to enable the FDA to assure that GE crops are safe to eat.”[12] Similarly, a Friends of the Earth review of company and FDA documents concluded:

“If industry chooses to submit faulty, unpublishable studies, it does so without consequence. If it should respond to an agency request with deficient data, it does so without reprimand or follow-up. . . . If a company finds it disadvantageous to characterize its product, then its properties remain uncertain or unknown. If a corporation chooses to ignore scientifically sound testing standards . . . then faulty tests are conducted instead, and the results are considered legitimate. In the area of genetically engineered food regulation, the ‘competent’ agencies rarely if ever (know how to) conduct independent research to verify or supplement industry findings.”[13]

At the end of the consultation, the FDA doesn’t actually approve the crops. Rather, they issue a letter including a statement such as the following:
“Based on the safety and nutritional assessment you have conducted, it is our understanding that Monsanto has concluded that corn products derived from this new variety are not materially different in composition, safety, and other relevant parameters from corn currently on the market, and that the genetically modified corn does not raise issues that would require premarket review or approval by FDA. . . . As you are aware, it is Monsanto’s responsibility to ensure that foods marketed by the firm are safe, wholesome and in compliance with all applicable legal and regulatory requirements.”[14]
The National Academy of Sciences and even the pro-GM Royal Society of London[15] describe the US system as inadequate and flawed. The editor of the prestigious journal Lancet said, “It is astounding that the US Food and Drug Administration has not changed their stance on genetically modified food adopted in 1992. . . . The policy is that genetically modified crops will receive the same consideration for potential health risks as any other new crop plant. This stance is taken despite good reasons to believe that specific risks may exist. . . . Governments should never have allowed these products into the food chain without insisting on rigorous testing for effects on health.”[16]

Promoting and regulating don’t mix

The FDA and other regulatory agencies are officially charged with both regulating biotech products and promoting them—a clear conflict. Suzanne Wuerthele, a US EPA toxicologist, says, “This technology is being promoted, in the face of concerns by respectable scientists and in the face of data to the contrary, by the very agencies which are supposed to be protecting human health and the environment. The bottom line in my view is that 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.”

Full article with footnotes at link:
http://www.seedsofdeception.com/utility/sh.../?objectID=1479
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http://www.democracynow.org/2010/2/10/headlines#7

February 10, 2010
India Blocks Sale of Monsanto GM Crop


India has put a halt to plans to allow genetically modified eggplant from the agri-giant Monsanto to be sold on the Indian market. On Tuesday, the Indian government reversed a decision to allow Monsanto to sell its eggplant crop, known as Bt Brinjal. It would have been India’s first genetically modified food crop
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Snuffysmith
India Defies Monsanto, Says No to GMO Crops

Posted: 10 Feb 2010 08:43 PM PST

We’ve followed the story of the slow but increasing and badly needed pushback against Monsanto’s predatory business practices, which force farmers to buy Monsanto seed annually, rather than re-use it. Worse, Monsanto seed has been genetically engineered so as to require the use of Monsanto herbicides and fertilizers.

And with (until recently) the seeds patent protected, farmers could be sued for having Monsanto genes in their crops. And with Monsanto having established a near monopoly in seeds, it has set prices so as to extract a higher percent of agricultural revenues than it could otherwise command. Needless to say, what is good for Monsanto is not at all good for farmers, as these excerpts from a Daily Kos post illustrates:

I am a small farmer, and I am deeply concerned about the broad power Monsanto and other seed companies wield. Their patents on life, unfair business practices, and aggressive genetic engineering of seed for commercial farming are making farmers dependent on their very expensive seed and killing the millennia-old practice of saving seed.

Since I was a child, the cotton business has been radically changed by developments like Round-Up Ready cotton. Farmers are forced by market pressures to adopt new practices, like using Monsanto seed, that are locking them into annual tithes to a monopolistic seed company. Monsanto, in particular, has forced hundreds of small seed companies out of the business with litigation and threats of litigation, and it’s no accident. Farmers are afraid to collect seeds at all, for fear that Monsanto will accuse them of patent infringement….

In visiting my husband’s family in Bangladesh, my brother-in-law complained about the lack of rice varieties available for consumption. In the past, hundreds of tasty varieties were available. Now only a very few with much less taste are on the market. These varieties, grown in the very unhealthy chemically dependent and unsustainable manner espoused by Monsanto to encourage the use of their many pesticides and herbicides, depletes the land and contaminate the waterways. Fish populations, on which the Bangladeshi population depends heavily for protein, are disappearing. Only the farm-raised varieties are in vast supply, those also being of less nutritional value and raised in polluted waters.

Monsanto’s hold on the seed market is especially problematic in that they also manufacture the chemicals with which the seeds are grown. This is forcing many farmers to use GMO seeds and unsustainable methods whether they want to or not. Neighboring farms (specifically, organic or those choosing to use non-GMO seeds) are having their seeds contaminated by the GMO varieties. Native varieties and hybrids, grown for 10,000 years and adapted to optimize local growing conditions, are bought up by Monsanto and removed from the market, denying options to farmers and consumers. Those not bought up are in danger of contamination by Terminator genes, which would lead to their extinction. The same way we protect animal species from extinction, we should protect plant species, especially the tens of thousands of food varieties, from companies like Monsanto that are consciously eliminating them. Would we allow genocide to occur in any other circumstance?

GMO crops have not been tested properly for safety. In India, farmers allowed their cattle to graze on GMO cotton plant stubble as they had grazed their cattle for millennia; all those cattle died within a few days. Many GMO varieties are neither better yielding nor requiring less fertilizer or water. They are designed to increase the use of Monsanto chemicals. These varieties are more expensive to grow, and the farmers are not allowed to save seed for the next year or the seeds have “Terminator” or “Traitor” genes to make new seeds sterile, causing them added expense. Monsanto’s methods are depleting the soil in areas already stressed.

I hope you will rein in these companies and start to restore a sense of fair play to agribusiness. Family farmers have enough to deal with without big chemical and seed companies holding them hostage.

The US courts have begun to whittle away at some of Monsanto’s efforts to monopolize seed production:

The Public Patent Foundation (PUBPAT) announced today that the United States Patent and Trademark Office has rejected four key Monsanto patents related to genetically modified crops that PUBPAT challenged last year because the agricultural giant is using them to harass, intimidate, sue – and in some cases literally bankrupt – American farmers. In its Office Actions rejecting each of the patents, the USPTO held that evidence submitted by PUBPAT, in addition to other prior art located by the Patent Office’s Examiners, showed that Monsanto was not entitled to any of the patents.
Monsanto has filed dozens of patent infringement lawsuits asserting the four challenged patents against American farmers, many of whom are unable to hire adequate representation to defend themselves in court. The crime these farmers are accused of is nothing more than saving seed from one year’s crop to replant the following year, something farmers have done since the beginning of time.

One study of the matter found that, “Monsanto has used heavy-handed investigations and ruthless prosecutions that have fundamentally changed the way many American farmers farm. The result has been nothing less than an assault on the foundations of farming practices and traditions that have endured for centuries in this country and millennia around the world, including one of the oldest, the right to save and replant crop seed.”

Raw Story describes the latest anti-Monsanto salvo, this by India :

India refused to grant permission Wednesday for the commercial cultivation of its first genetically modified (GM) food crop, citing problems of public trust and “inadequate” science.

Environment Minister Jairam Ramesh said he was imposing a moratorium on the introduction of an aubergine modified with a gene toxic to pests that regularly devastate crops across India.

“It is my duty to adopt a cautious, precautionary, principle-based approach and impose a moratorium on the release,” until scientific tests can guarantee the safety of the product, said Ramesh…

“I cannot go against science but in this case science is inadequate,” he added. “I have to be sensitive to public concerns.”

Indian regulators had approved the new aubergine back in October and its introduction would have made it the first GM foodstuff to be grown in India.

But the decision roused huge opposition and a broad spectrum of voices, including farmers, environmentalists and politicians of all stripes had urged the government to prevent its cultivation…

Ramesh said there was “no overriding food security argument” for the introduction of GM aubergines.

He said he had considered the views of different interest groups in making his decision but denied he had been pressured by members of his cabinet or by companies producing genetically modified crops.

“My conscience is clear. This is my decision and my decision alone,” he said.

India is one of the largest aubergine producers globally.

Reader John D, who pointed us to the piece, adds:

They are fighting Monsanto trying to patent the genes from their indigenous plants.

The history of GMO crops in India is like elsewhere. The first few years are great then they need more herbicide and more fertilizer to get yields and that drives the farmer into bankruptcy. India has had a rash of farmer suicides due to crop failures. They didn’t have this with indigenous seeds. The costs were much less and they could muddle through.

The concerns about safety are also legitimate. As Scientific American pointed out:

Unfortunately, it is impossible to verify that genetically modified crops perform as advertised. That is because agritech companies have given themselves veto power over the work of independent researchers.

…Under the threat of litigation, scientists cannot test a seed to explore the different conditions under which it thrives or fails. They cannot compare seeds from one company against those from another company. And perhaps most important, they cannot examine whether the genetically modified crops lead to unintended environmental side effects.

Research on genetically modified seeds is still published, of course. But only studies that the seed companies have approved ever see the light of a peer-reviewed journal. In a number of cases, experiments that had the implicit go-ahead from the seed company were later blocked from publication because the results were not flattering. “It is important to understand that it is not always simply a matter of blanket denial of all research requests, which is bad enough,” wrote Elson J. Shields, an entomologist at Cornell University, in a letter to an official at the Environmental Protection Agency (the body tasked with regulating the environmental consequences of genetically modified crops), “but selective denials and permissions based on industry perceptions of how ‘friendly’ or ‘hostile’ a particular scientist may be toward [seed-enhancement] technology.”

Some research recently raised questions on the adequacy of Monsanto’s research on the health of GMOs (a mere 90 days) and some small scale animals studies have found consumption of Monsanto GM products are associated with organ damage. One reader noted:

I am fairly well-qualified to comment on this, as both a PhD in genetics who has made hundreds of transgenic plant lines (albeit in Arabidopsis) and a former Nature editor.

I don’t doubt for a second that Monsanto has failed to adequately investigate the potential negative effects of BT toxin (MON 810 and MON 863) and bar (NK 603) overexpression and possible toxicity. This is even more warranted by the fact that these genes are being regulated by a strong viral promoter (CaMV35S) that is producing levels of these proteins that far exceed what would normally occur in a plant–even though these gene products don’t normally in plants. (Both genes are bacterial in origin.)

That’s a long winded way of saying concerns about Monsanto, from both a health and economic perspective, are far from alarmist.


http://www.nakedcapitalism.com/2010/02/ind...d+capitalism%29
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http://www.organicconsumers.org/articles/article_20196.cfm

Brazilian Farmers Declare War on Monsanto

GM Watch, Feb 9, 2010
Straight to the Source: http://www.gmwatch.org/

ABSTRACT: When it arrives at the warehouses the grain is tested and identified as GMO or non-GMO. The problem occurs when, in many cases, conventional oleaginous seeds are contaminated and the growers end up having to pay royalties [to Monsanto] without having acquired any GMO seeds in the first place.

Marcondes Maciel and Tania Rauber
Diario de Cuiaba [Brazil], 29 January 2010

http://www.diariodecuiaba.com.br

In Cuiaba, Aprosoja is preparing a court action against Monsanto, and in Sinop, steps are being taken to follow suit

[English translation courtesy Cert ID Brazil and GM-free Ireland]

Growers in [the Brazilian State of] Mato Grosso have declared war against Monsanto, the multinational corporate owner of the GMO soya technology known as RR (Roundup Ready). After exhausting all attempts to engage the company in dialogue, the growers are now considering legal action. In Cuiaba, Aprosoja (the Association of Soya and Corn Producers Association of the State of Mato Grosso) is preparing a lawsuit. In Sinop (500km North of Cuiaba) the growers are looking to sue the company as well.

Aprosoya wants to determine if the [patent] royalty fee paid by the soya growers is actualy due. "We want to know what sort of patent is generating this type of fee, because depending on the type, the company does not have the right to charge us anything at all. We also need to know the patent's validity period," explains the President of Aprosoja, Mr. Glauber Silveira.

In Mato Grosso, growers increased the cultivated area of GMOs from 2.6 million hectares (2008/09 crop) to approximately 3 million hectares in this year's crop. The expansion of the area will increase Monsanto's profit from R$39 million (*15.2m) to R$45 million (*15.6m), an increase of 15.38%. According to calculations made by the producers, the fee Monanto charged for the use of its patent amounts to R$15.00 (*5.85) per hectare.

Aprosoja intends to issue a notification demanding that Monsanto provide proper justification regarding the royalty fees. "We have been informed that Monsanto is inducing the seed producers of Mato Grosso to provide only GMO seeds", denounces Mr. Silveira. In Mato Grosso the GMO plantation now occupies half of the entire cultivated area of soya, comprising about 6 million hectares.

SINOP - Following several meetings without any positive results, the Sinop Rural Union is also planning to sue Monsanto. Approximately 50% of the crop fields in the Northern Region of Mato Grosso are currently cultivated with GMO varieties. These differ from the conventional because of their resistance to herbicides containing glyphosate, used in desiccation before and after planting to eliminate all kinds of weeds.

This kind of resistance enables the growers to apply the herbicide on the soya only, thus reducing their production costs and the number of herbicide applications. But the sectors' questions concern the royalty fees imposed by Monsanto for their use of the seed.

The president of the Union, Mr. Antônio Galvan, explained that two collections are made: The first one being when the seed is bought (by bank order). "In January they charged R$0.45 per kilo of seed, which is equivalent to 30% of the price of each sack.

The main questioning lies on the second collection which is made when the product is leaving the fields. When it arrives at the warehouses the grain is tested and identified as GMO or non-GMO. The problem occurs when, in many cases, conventional oleaginous seeds are contaminated and the growers end up having to pay royalties without having acquired any GMO seeds in the first place.

This contamination occurs in the fields by means of pollination or at the time of planting, as well as at the time of stocking the harvest. "Cross pollination may take place if there's a field of GMO soya next to a Non-GMO one at flowering time. Contamination can also take place if the machines are not well cleaned at harvest time, and some GMO beans remain. In this way, they will be considered GMO when they are tested".

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Anti-GMO petition discussion here (134 comments including one organic farmer and two recalcitrant skeptics):
http://www.democraticunderground.com/discu...7699580#7716256
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http://www.huffingtonpost.com/jeffrey-smit...e_b_473088.html

PLU Codes Do NOT Indicate Genetically Modified Produce

By Jeffrey Smith
Posted: February 23, 2010 11:02 AM


Let's put a rumor to rest. No, the 5-digit PLU codes on produce do NOT tell you what is genetically modified or natural. This urban legend has circulated long enough, even on the best of websites. It's time to take it down.

The 4-digit PLU codes on the sometimes-pain-in-the-neck labels glued to apples, for example, tell the checkout lady which is a small Fuji (4129) and which is a Honeycrisp (3283). She'll know what to charge you and the inventory elves will know what's what. If there's a 5-digit code starting with 9, then it's organic.

These numbers, organized by the Produce Marketing Association, have nothing to do with you. According to Kathy Means, Association Vice President of Public Relations and Government Affairs, this is an optional convention for retailers and their supplier and is NOT designed as a communication tool for customers. If you want to know which items are organic, look for the word Organic; and stop squinting at tiny codes.

GMO codes are hypothetical

Those that run PLU-universe figured that someday some retailer might want to distinguish between a GMO and a non-GMO for price or inventory purposes. So they created a convention of 5 digits starting with an 8, just in case it catches on. But it hasn't. No one uses that number 8 as far as we can tell. And why would they? Most Americans say they would avoid GMOs if they were labeled.

Some seed companies don't even want gardeners to know which seed is genetically modified. One company that sells zucchini seeds outfitted with virus genes announced that they would refuse to sell seed packets in Vermont, since the state legislature requires GM seeds to be labeled.

Shopping Guide helps you avoid GMOs

Where does that leave you—if you happen to be one of those finicky eaters who value your immune and reproductive systems, and don't want your kids to end up with the organ damage common among GMO-fed lab animals?

Fortunately, we've got you covered. Go to http://www.nongmoshoppingguide.com/SG/Home/index.cfm and peruse the long lists of non-GMO and GMO brands by category. Download a two-page version, order or download the pocket guide http://www.nongmoshoppingguide.com/documentFiles/144.pdf , or even equip your iPhone with the new app "ShopNoGMO".

Although a list of non-GMO brands won't help you figure out if your produce is genetically modified, the great news is that there are only 4 GMO veggies or fruits at this point: papaya, but only from Hawaii and no where else; some zucchini and yellow squash, and some corn on the cob. For these, unless it says organic or boasts a non-GMO sign in the store, eating them is a gamble. It could be GMO.

If you're not sure if GMOs are bad for you, we've got you covered there too. Visit http://www.responsibletechnology.org/GMFree/Home/index.cfm and read, listen, or watch, and find out why more and more doctors and medical organizations are prescribing non-GMO diets to all patients.


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http://indiatoday.intoday.in/site/Story/85...html?complete=1



Anti-GM activists denied visa

New Delhi February 24, 2010

The new proposal to jail anyone questioning the safety of genetically modified (GM) crops has yet to become a law. But the government appears to have already started muzzling anti-GM voices, environmental activists have alleged.

A regional government official and a professor of genetics from Italy - both important members of the GM-free movement - have been allegedly denied visa by the Indian government.

The two were supposed to speak at an international conference on "genetically modified organism-free movement" organised by the Research Foundation for Science, Technology and Ecology in Delhi on Tuesday.

Maria Grazia Mammucini is the director of the regional government of Tuscany's agency for agriculture, while Marcello Buiatti is a professor of genetics at the University of Florence and a member of the European Network of Independent Scientists.

They have played a key role in getting regions in Europe declared GM-free and were supposed to share their experience at the meeting.

The agriculture agency of the Region of Tuscany headed by Mammucini was listed as one of the co-hosts of the event. Tuscany is one of the 49 regions in Europe that have officially declared themselves GM-free. In India, 13 states have so far said no to Bt brinjal and only Kerala has declared itself
GM-free.

Vandana Shiva, who heads the organisation hosting the meeting, alleged: "The visa has been denied at the behest of the agriculture ministry which is headed by pro-GM politician Sharad Pawar. Both Mammucini and Buiatti have valid papers, including an invitation from us. There was no reason they should have been denied entry into India." "When I contacted the Indian embassy, the official there told me that he needed permission from the agriculture ministry for issuing the visas," Shiva added.

"This arbitrary action has denied the Indian public a chance to hear Prof. Buiatti who has shown how genetic engineering is unreliable and risky."Shiva criticised Pawar for his alleged move to get the recent moratorium on Bt brinjal lifted.

"It seems the PM (Manmohan Singh) has said (environment minister) Jairam Ramesh can't have the last word on Bt brinjal. The fact is that the people have had the last word on this subject and politicians can't be allowed to undo that,"she said.

Shiva said the proposal to set up the Biotechnology Regulatory Authority of India was aimed at deregulating the biotech industry and not at safeguarding biosafety. The existing biosafety framework, she said, was good enough. It only needed transparent implementation.

Benedikt Haerlin, a former member of the European parliament, said that while cultivation of GM crops was legal in many regions of Europe, it was the public pressure that was keeping the regions free of GM foods.

Debi Barker of the Center for Food Safety in Washington said it was a myth that GM crops in the US had brought down pesticide use or increased yields.


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From a blog at a website for employees at Stanford, as far as I can tell, an overview article.

QUOTE
http://stanford.wellsphere.com/organic-foo...-m-smith/766671



Doctors Warn: Avoid Genetically Modified Food
By Jeffrey M. Smith
Posted Aug 10 2009 4:33pm


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QUOTE
http://www.lavidalocavore.org/diary/3357/e...r-monsanto-case

Ex Monsanto Lawyer Clarence Thomas to Hear Major Monsanto Case

by: dsnodgrass (promoted by Jill Richardson)
Tue Mar 09, 2010 at 09:19:13 AM PST


In Monsanto v. Geertson Seed Farms, No. 09-475, the U.S. Supreme Court will hear arguments in a case which could have an enormous effect on the future of the American food industry. This is Monsanto's third appeal of the case, and if they win a favorable ruling from the high court, a deregulated Monsanto may find itself in position to corner the markets of numerous U.S. crops, and to litigate conventional farmers into oblivion.

Here's where it gets a bit dicier. Two Supreme Court justices have what appear to be direct conflicts of interest.

Stephen Breyer

Charles Breyer, the judge who ruled in the original decision of 2007 which is being appealed, is Stephen Breyer's brother, who apparently views this as a conflict of interest and has recused himself.

Clarence Thomas

From the years 1976 - 1979, Thomas worked as an attorney for Monsanto. Thomas apparently does not see this as a conflict of interest and has not recused himself.

Fox, meet henhouse.




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believe_it
QUOTE
http://www.lavidalocavore.org/diary/3357/e...r-monsanto-case

Ex Monsanto Lawyer Clarence Thomas to Hear Major Monsanto Case

by: dsnodgrass (promoted by Jill Richardson)
Tue Mar 09, 2010 at 09:19:13 AM PST


In Monsanto v. Geertson Seed Farms, No. 09-475, the U.S. Supreme Court will hear arguments in a case which could have an enormous effect on the future of the American food industry. This is Monsanto's third appeal of the case, and if they win a favorable ruling from the high court, a deregulated Monsanto may find itself in position to corner the markets of numerous U.S. crops, and to litigate conventional farmers into oblivion.

Here's where it gets a bit dicier. Two Supreme Court justices have what appear to be direct conflicts of interest.

Stephen Breyer

Charles Breyer, the judge who ruled in the original decision of 2007 which is being appealed, is Stephen Breyer's brother, who apparently views this as a conflict of interest and has recused himself.

Clarence Thomas

From the years 1976 - 1979, Thomas worked as an attorney for Monsanto. Thomas apparently does not see this as a conflict of interest and has not recused himself.

Fox, meet henhouse.




The lawsuit was filed by plantiffs which include the Center for Food Safety, the National Family Farm Coalition, Sierra Club, Dakota Resources Council and other farm, environmental and consumer groups and individual farmers. The original decision ( http://ohioaglaw.wordpress.com/2010/01/20/...-supreme-court/ ):
The federal district court in California issued its opinion on the deregulation of “Roundup Ready” alfalfa pursuant to the Plant Protection Act on February 13, 2007. Upon receiving Monsanto’s petition for deregulation of the alfalfa seed, APHIS conducted an Environmental Assessment and received over 500 comments in opposition to the deregulation. The opposition’s primary concern was the potential of contamination. APHIS, however, made a Finding of No Significant Impact (FONSI) and approved the deregulation petition, thereby allowing the seed to be sold without USDA oversight. Geertson Seed Farms, joined by a number of growers and associations, filed claims under the National Environmental Policy Act (NEPA) as well as the Endangered Species Act and Plant Protection Act. In regards to NEPA, they argued that the agency should have prepared an EIS for the deregulation.

Addressing only the NEPA claims, the court agreed that APHIS should have conducted an EIS because of the significant environmental impact posed by deregulation of the alfalfa seed. A realistic potential for contamination existed, said the court, but the agency had not fully inquired into the extent of this potential. The court also determined that APHIS did not adequately examine the potential effects of Roundup Ready alfalfa on organic farming and the development of glyphosate-resistant weeds and that there were “substantial questions” raised by the deregulation petition that the agency should have addressed in an EIS. Concluding that the question of whether the introduction of the genetically engineered alfalfa and its potential to affect non-genetic alfalfa posed a significant environmental impact necessitated further study, the court found that APHIS’s decision was “arbitrary and capricious” and ordered the agency to prepare an EIS. The court later enjoined the planting of Roundup Ready alfalfa from March 30, 2007, until completion of the EIS and reconsideration of the deregulation petition, except for those farmers who had already purchased the seed. In May of 2007, the court enjoined any future planting of the alfalfa. An order by the court in June, 2007 required disclosure of all Roundup Ready planting sites.
Monsanto filed appeals in 2008 and 2009. In both instances, they were unsuccessful in having the original decision reversed, so they appealed to the Supreme Court, who agreed to hear the case.
Alfalfa is the fourth most widely grown crop in the United States, behind corn, soybeans, and wheat.

South Dakota alfalfa farmer Pat Trask, one of the plaintiffs, said Monsanto's biotech alfalfa would ruin his conventional alfalfa seed business because it was certain his 9,000 acres would be contaminated by the biotech genes.

Alfalfa is very easily cross-pollinated by bees and by wind. The plant is also perennial, meaning GMO plants could live on for years.

"The way this spreads so far and wide, it will eliminate the conventional alfalfa industry," said Trask. "Monsanto will own the entire alfalfa industry."

Monsanto has a policy of filing lawsuits or taking other legal actions against farmers who harvest crops that show the presence of the company's patented gene technology. It has sued farmers even when they have tried to keep their own fields free from contamination by biotech plants on neighbouring farms.
The case has implications beyond alfalfa crops. About eight hundred reviewed genetically engineered food applications were submitted to the USDA, yet no environmental impact statements were prepared. Even as this diary is being written, a federal judge in San Francisco is reviewing a similar case involving genetically modified sugar beets. The decision is expected this week and could halt planting and use of the gm sugar beets, which account for half of America's sugar supply.

Back to the Supreme Court case, oral argument is slated to begin on April 27, 2010. With Breyer recused and Thomas opting not to recuse, the bench appears to be heavily tilted to Monsanto.

Once more with feeling. Fox, meet henhouse.



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http://www.abanet.org/publiced/preview/bri...010.shtml#09475

Tuesday, April 27, 2010
Monsanto Co., v. Geertson Seed Farms, Docket No. 09-475

ABA posting of Merit and Amicus Briefs


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QUOTE
http://www.supremecourtus.gov/oral_argumen...alApril2010.pdf

UNITED STATES
09-475
Tuesday, April 27 (3) MONSANTO CO. V. GEERTSON SEED FARMS
Court convenes at 10 a.m.


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http://origin.www.supremecourtus.gov/docket/09-475.htm

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