Archive for category: Organics/GM

NEW EU ORGANIC REGULATIONS ATTRACT EXPERT SCRUTINY

The new Organic Regulation – status quo and outlook

 by Karin Heinze

Part of panel discussing pro and contra of the new EU Organic Regulation.

Part of panel discussing pro and contra of the new EU Organic Regulation. From the left side: Toomas Kevvai, Deputy Secretary-General for Food Security and Development of the Rural Ministry of Estonia, Elena Panichi, Deputy Head of the Organic Unit DG AGRI, European Commission and Professor Nic Lampkin, Organic Research Centre, UK.© Karin Heinze

At the IFOAM EU Organic Congress in Tallinn representatives of the EU and of the organic sector discussed pro and contra of the new European Organic Regulation. After a record time of more than three years and 18 trilogues Regulatino probably will be launched in June 2020, although neither the Council and Commission nor the Parliament and the stakeholders of the organic sector are completely satisfied with the compromise.

At the panel discussion moderated by Markus Arbenz Managing Director of IFOAM Organics International, Elena Panichi, Deputy Head of the Organic Unit DG AGRI, European Commission, looked back to the very long negotiations about the proposal of the Commission. She explained that the negotiated compromise that was found under the EU-presidency of Malta in June will be the base of the further working out of the Regulation.

She expects the final meetings of the Commission and the Council for the Regulation in October/ November and after that the vote of the Parliament. Ms. Panichi was confident that the Regulation will be a harmonization of the organic law for all EU members. Toomas Kevvai, Deputy Secretary-General for Food Security and Development of the Rural Ministry of Estonia, which has the EU Presidency till the end of the year, said “certainly it is a compromise but that from the view of the member states it is acceptable.

Markus Arbenz, IFOAM Organics International, moderated the panel.

Markus Arbenz, IFOAM Organics International, moderated the panel. From the left side: Prof. Nic Lampkin, Markus Arbenz, Martin Häusling (MEP), translator, Thomas Fertl (IFOAM EU Board) © Karin Heinze

Martin Häusling, Member of the European Parliament and chief negotiator for the Organic Regulation emphasised: “Nobody is really and completely satisfied with the compromise paper. But after three years of negotiations I can say that we reached a draft that has an added value for the organic sector.” He added: There are 600 pages of the text and you must not only look at some problematic issues, because there is a true potential to make a the Regulation a senseful tool for the sector. As Professor Nic Lampkin from the Organic Research Centre in UK said, organic is much more than commodities free from pesticides. He explained that he can understand the unsecurity about this new regulation but he also reassures that there will be ways to handle the new regulation.

Associations call for further improvements

Thomas Fertl Board Member of IFOAM EU and BioAustria explained that he, IFOAM and other organic associations could not see the added value for the organic sector. He said: “It is no secret that the organic sector was not asking for a new regulation and that associations are sure that the work on the current regulation would have been more fruitful than a new draft.” Among others he quoted the regulations for residues in the draft and the import issues.
Professor Nic Lampkin outlined that there is the need of a regulation, but it should be a baseline and not a prison for organic producers. If rules are too restrictive and block the producers in their activities and innovation the regulation is on a wrong way. „In fact the Regulation should encourage organic farmers“, he said.

The participants from all over Europe listened the interesting discussions.

The participants from all over Europe listened the interesting discussions. © Karin Heinze

Private activities are welcome

Elena Panichi explained that every party in the process has its own role. She reminded the panel and the auditorium also that there are many other tools in the EU and that private activities are very welcome. An example is the European Innovation Partnership that brings new ideas also to the organic sector. Ms. Panichi also mentioned new tool that should strengthen farmers and there private along the food chain were more than welcome. On a global level there is a new initiative called ´plurilateral meets` that is involving the biggest players in the organic sector like the US, Canada, Europe, Switzerland, Chile, Japan and South Korea. In these talks the harmonisation of the international rules is discussed. This should make international trade easier and lower the burden for farmers and traders, Panichi said. Martin Häusling reqired fair rules for international competition.

Source=http://organic-market.info/news-in-brief-and-reports-article/the-new-organic-regulation-status-quo-and-outlook.html

AFRICAN CENTRE REPORTS ON FISP IN MOZAMBIQUE

African Centre for Biodiversity <webmaster@acbio.org.za>

ACBioThe African Centre for Biodiversity
www.acbio.org.za
PO Box 29170, Melville 2109 South Africa
Tel: +27 (0)11 486 1156

Dear Friends and colleagues

The African Centre for Biodiversity (ACB), shares with you the position of civil society organisations on  Farm Input Subsidy Programme in Mozambique.

The CSO statement criticizes the farm input subsidy programme (FISP of the government of Mozambique, which promotes the use of hybrid seed, toxic agrochemicals, ecologically harmful synthetic fertilisers and expensive agricultural implements and machinery.

During the period 2007-2013, the Mozambican government spent a staggering $1.1-billion on synthetic fertiliser programmes, creating enormous profits for fertiliser companies. Despite this expenditure, the agricultural sector is far from securing sufficient nutritious food for 25 million Mozambicans.

For CSOs in Mozambique, the way in which the FISP is structured, it is creating high levels of farmer dependency on expensive agricultural inputs, reducing seed and crop diversity, while threatening to make farmers’ seeds obsolete. The program is also bolstering the monopoly of companies that produce and supply farm inputs and creating enormous ecological problems such as damage to the soils through the use of synthetic fertilisers. FISP is also deepening inequalities between small-scale and commercial farmers. According to the groups, this kind of programme does not build a sustainable agricultural system able to cope with economic pressures and the effects of climate change.

As an alternative to the current FISP, the CSOs are encouraging their government to support an agricultural system that promotes agro-ecological practices for food, feed and fibre production. This includes the promotion and use of indigenous seed and respect for and maintenance of traditional knowledge and cultural traditions and practices.

Kind regards ACB team

22 Oct 2017

Source=www.acbio.org.za

 

AFRICA WARNS !!!—–NO SAFE LIMITS FOR TOXIC PESTICIDES

Recall that Nigeria is still under ban by the EU for unacceptable levels of a pesticide–dichlorvos on her beans

Now, the African Centre for Biodiversity (formerly African Centre for Biosafety) has come out to frown at the continued use of what it called ‘questionable’ data  on pesticides  by African countries.  The South Africa based centre published a report titled  ‘No Safe Limits for Toxic Pesticides in our foods’ in July 2017. The Maximum Residue Limits now seems suspect

No established safe levels
for toxic pesticides
The safe levels for pesticides that are
determined by regulators have been widely
scrutinised for being outdated, inadequate
and heavily influenced by industry, which has
even participated in the regulatory approvals
of glyphosate for the EU, making the integrity
of the entire process questionable. Some
of the concerns surrounding the approval
process and the acceptable daily intake (ADI)
doses include:
1.
Tests rely on industry studies alone,
which remain unpublished and kept as
confidential commercial secrets. This
means that data cannot be independently
scrutinised and comes with clear conflict
of interest.
2.
Only the active ingredient is tested,
despite the fact that certain adjuvants
added to commercial formulations are
toxic and has also been shown to increase
toxicity of the active ingredient itself
(Mesnage et al., 2014).
3.
Most regulatory tests are more than
20 years old for glyphosate, 2,4-D and
glufosinate and therefore have not taken
into account recent independent data
showing toxicity.
4.
No tests are done on low doses that are
below the ADI.
5.
Combinatorial effects of multiple
pesticides are not tested.
6.
The ADI differs in various regions, from the
EU to China, the United States and South
Africa, questioning a scientific consensus on safety
For full report  please visit==https://acbio.org.za/wp-content/uploads/2017/07/No-Safe-Limits-for-Toxic-Pesticides-in-Our-Food.pdf
Sept 2017

 

MOSANTO HAS JOB FOR YOU AT ABUJA

Technology Development Representative-Nigeria
MONSANTO 1,157 reviewsAbuja
Monsanto’s Technology Development and Agronomy Team in sub-Saharan Africa is hiring for a Technology Development Representative to be part of a team that lead the development and testing of agronomic system concepts for our products. This role will gain firsthand knowledge of Monsanto’s products and associated agronomic systems research to provide technical leadership and conduct field research within Nigeria. This includes, understanding local and regional cropping systems and the development of existing and newer pipeline products. Successful candidates must have strong communication and people skills to enable cross-functional interactions with R&D and commercial teams.

Key Responsibilities: Coordinate and execute systems field testing program that supports maize and/or cotton germplasm and trait evaluations across different agroecological zones. Responsible for all aspects of coordination and execution of field trials in alignment with commercial team; trial seed forecasting, location identification, cooperator contracts, trial design, planting, in-season trial maintenance, data recording, harvesting and relinquish data. Active contribution and advancement team’s work, proposals for variety advancements. Maintain country regulatory compliance, ensure trials are conducted within regulatory and stewardship policy and paperwork is accurately completed in a timely manner.

Develop and maintain relationships with Technology Development colleagues to help steward current products and introduce new products. Regularly integrate emerging technology tools to improve work efficiency and execution of assigned responsibilities. Provide technical leadership for local sales organization through agronomic trainings, product and technology scientific knowledge transfer and stewardship initiatives. Technical contribution in demand generating activities like customer visits, demonstration plots, farmer field days and events, marketing tools, etc.

Investigation of product performance inquiries that require specific agronomic and product knowledge. Maintain and build relationship with researchers from academic and research institutions. Ensures equipment is properly maintained, operating and ready for use. Actively participate in the site safety program.

 

 

Source=https://ng.indeed.com/job-description? 24 Sept 2017

ELECTRICITY FROM HUMAN WASTES

Dutch designers use human waste to make electricity

By Bongani Shwen

 

The Compost Kliko Toilet could lead to people getting away from flushing potential down the toilet…

etabolism and cut crop productivity, ultimately putting pressure on arable land…

26 Jun 2017

Dutch designers use human waste to make electricity

For more, visit http://www.bizcommunity.com/196/642.html

New Health Risks of GM Mosquitoes and Salmon ??

Just when genetically modified (GM) mosquitoes got their approval by the Cayman Islands and the government of Canada’s Prince Edward Island is trying to approve GM salmon, new research reveals unexpected and potentially dangerous effects of genetic engineering. Unfortunately, neither the makers of genetically modified organisms (GMOs) nor their regulators conduct the studies that are necessary to protect the public. Being bitten by GM mosquitoes and eating GM salmon remains a serious gamble.

The new discomfiting research published in Nature Methods[1] examined the unintended impacts of gene editing on the DNA of mice. Gene editing is touted by its promoters as the safer, more precise version of genetic engineering. The earlier version that was used to create the GM crops we all know about (soy, corn, etc.) forced genetic material from bacteria or viruses into plant DNA. Gene editing, on the other hand, does not necessarily introduce genes from foreign species. Rather, it cuts the DNA in a predetermined location. The cell’s DNA repair mechanisms are then activated to repair the cut.

Of all the gene editing techniques, the one that is easiest, least expensive, and most popular is called CRISPR-Cas9. Proponents claim it is so safe and predictable, it should not be regulated. They want to put their gene-edited products on the market without informing governments or consumers. And they don’t even want it to be called genetic engineering, since consumers have largely weighed in against GMOs. That is why the recent research is so damning.

Gene Editing Creates Predictable Mutations

The tools used for gene editing are designed to recognize and make changes only on specific DNA sequences. In the Nature Methods research, for example, the engineers designed their tools to fix a defective DNA sequence that could restore sight to blind mice. But the defective DNA sequence that governs sight is also repeated in other places throughout the mouse genome—unrelated to vision. Therefore, the gene editing tools can also make unintended changes in these “off-target” locations.

The unwanted mutations do not come from cutting the DNA. Rather, they occur when the cut ends are rejoined by the cells’ repair mechanisms. It results in either the loss of some DNA base units or the insertion of a few base units at the cut site.

If the mutation occurs in the middle of a known gene (or in a portion of the DNA that controls a gene) it can severely disrupt its function. Gene editors, therefore, rely on computer models of the genome to identify where the similar sequences are that are likely to become mutated and to predict what level of collateral damage that could create. If the risk is considered low enough, they proceed with editing.

Widespread Unpredicted Mutations Discovered

There is a joke that says molecular biologists don’t understand just two things: molecules and biology. Too often, the complex 3-D world doesn’t cooperate with their computer model predictions. This was again confirmed by the work of Stamford’s Dr. Kellie Schaefer, along with her colleagues from Stamford, Columbia, and the University of Iowa.

Instead of letting the computer guess which off-target changes would take place, Schaefer’s team actually sequenced the genome of the two gene-edited mice after they had undergone CRISPR-Cas9. They did find insertions and deletions (indels), which is the type of mutation that the computer predicts. One mouse had 164 indels; the other 128. But of the top 50 sequences that a computer would identify as most likely to be mutated, none were changed at all. Far more importantly, however, the computer model would totally miss their other finding: point mutations throughout the genome. One mouse had 1,736; the other 1,696.

A point mutation is the replacement of a single nucleotide along the DNA. But don’t let its smallness fool you. These so-called single-nucleotide variants (SNV) can have huge consequences. They can lead to many types of changes, including disease.

According to Dr. Michael Antoniou, a London-based molecular geneticist who routinely uses genetic engineering in his research, “Many of the genome editing-induced off-target mutations [both the point mutations and the indels] . . . will no doubt be benign in terms of effects on gene function. However, many will not be benign and their effects can carry through to the final marketed product, whether it be plant or animal.”[2] This could translate into possible toxins, allergens, carcinogens, or other changes that could affect those eating a GMO.

Dr. Michael Hansen, a Senior Scientist at Consumers Union, the policy arm of Consumer Reports, wrote, “While genome editing has been portrayed in the media as an incredibly precise process, where one can go in and literally only intentionally change one or a small number of nucleotide bases, the reality is that there can be large numbers of off-target effects.” He says, “This study raises troubling concerns.”

Another recently published study in Nature Communications used CRISPR/Cas9 to make 17 edits in the mouse genome. They too sequenced the genome and found unexpected insertions and deletions in all 17 places. Whereas deletions of approximately 9 base pairs are predicted, the actual size of the deletions was as high as 600 base pairs. No computer model predicts DNA damage this extensive.

A third study published this year[5] also found deletions of more than 500 base units. The researchers also confirmed that proteins produced by these mutated sections were altered. Such changes could theoretically transform a beneficial protein to a harmful one.

Hansen says the long deletions of DNA material “may not be routinely identified without whole genome sequencing.” But whole genome sequencing is rarely done by gene editors. Instead, they rely on their computers.

Even if they did sequence the genome, science doesn’t yet have the capacity to predict what the real-life consequences of all the mutations would be. Therefore, according to Antoniou, “it is also essential to ascertain the effects of these unintended changes on global patterns of gene function.” For this, both Antoniou and Hansen (as well as the National Academy of Sciences[6] and the international standard setting body Codex Alimentarius[7]) agree that the scientists must also analyze the changes in RNA, proteins, and metabolites.

Armed with this data, certain problems would be obvious—an increase of a known allergen or toxin, for example. But even if no red flags are raised at this point, according to Antoniou, “it is still necessary to conduct long-term toxicity studies” using animals. That’s because, once again, science is still not competent to figure out the complex interactions and side effects that can occur.

Antoniou concludes, “In the absence of these analyses, to claim that genome editing is precise and predictable is based on faith rather than science.”

And it is mere faith that supports the claims that GM mosquitoes and salmon are safe. Although they were not produced by the CRISP-Cas9 technique, they are the product of earlier gene-insertion techniques, which are also fraught with unpredictable mutations and altered gene expressions.

Earlier Research Warnings Ignored by GMO Makers

Just because this year’s research on gene editing shows unintended and potentially dangerous side effects does not mean that companies using the technology will change the way they operate. Indeed, back in 1999, a study showed widespread changes in the DNA due to gene insertion; but many GMO companies conveniently ignored the findings and continue to do so.

In that study, scientists studying cystic fibrosis inserted a gene into human cells.[8] Using a microarray, they discovered that the insertion “significantly affect[ed] up to 5% of the total genes in the array.” This means that the presence of a single foreign gene might change the expression of hundreds, possibly thousands of genes. In the case of the human cell being studied, the scientists were at a loss to determine the impact. “In the absence of more biological information,” they wrote, “we cannot discern which directions are better or worse, since any of these may have positive or negative effects.”

Just like the recent gene editing studies, this 1999 discovery contradicted the assumptions of an entire industry, which marched forward on the false assumption that their GMOs were predictable and safe.

The Untested Danger of a GM Mosquito Bite

In January 2014, I testified at the Florida Keys Mosquito Control District, opposing their planned release of GM mosquitoes. Also testifying was Derric Nimmo, a principal scientist at Oxitec, the UK company that produces the mosquitoes.

Oxitec had already conducted limited releases with millions of Aedis Aegypti mosquitoes in the Cayman Islands, Brazil, Panama, and Malaysia. The male insects were engineered to mate with natural females and produce offspring that die before reaching adulthood. Their plan was to reduce the population and thereby reduce the incidence of dengue and other diseases that this type of mosquito carries.

The company had widely publicized that they were only releasing males, which don’t bite. But it turns out that their method of sorting males from females is flawed, and thousands of biting female mosquitoes are released.[9] In addition, their method to create non-viable offspring is also flawed. Between 3%-15% of the offspring survive and prosper.[10] This can easily translate into millions of biting females, born from a genetically engineered family tree.

After the Florida hearing was over, I asked Derric if they ever analyzed the saliva from their GM mosquitoes, since the saliva enters the bloodstream of the people who are bitten. He said that they were just now doing research to see if the protein produced by the inserted gene was found in the saliva.

Realizing that they had already exposed the population of four countries to their mosquito saliva before doing this research, I was unimpressed. Then…

I explained to Derric the findings of the cystic fibrosis study, showing that a single inserted gene can create widespread changes, including new toxins, allergens, or carcinogens. Shouldn’t his company analyze everything in the saliva, I asked? Derric responded, “Good idea.”

ln Derric’s defense, Oxitec is not the only company that is tampering with nature’s gene pool in spite of the fact that it is wholly unprepared and unqualified to do so. Other GMO makers also fail to use the modern molecular profiling techniques that reveal unintended side effects. However, when independent scientists conduct that type of research on GMOs, the results are sobering.

For example, long after Monsanto’s Roundup Ready corn had been consumed by hundreds of millions of people, a team led by Dr. Antoniou[11] found more than 200 significant changes in its proteins and metabolites, compared to non-GMO corn of the same variety. Two of the compounds that increased are aptly named putrescine and cadaverine, because they produce the horrific smell of rotting dead bodies. More worrisome; they are also linked to higher risks of allergies and cancer. Another Monsanto GM corn has a new allergen[12] and their cooked soy has up to seven times the level of a known soy allergen, compared to cooked non-GMO soy.[13]

The Typical Biotech Response: Ignore or Attack

If regulators and medical authorities knew in advance that a proposed GMO contained new or higher levels of dangerous allergens, it is unlikely that the GMO would have been introduced. (I’m being optimistic.) But once a GMO variety is released, grown on millions of acres and eaten by millions of people, somehow the crop enjoys a bizarre immunity. Confronted with hard evidence of allergens, GMO makers and government regulators typically ignore the problem. The offending GMOs are still on the market, and they don’t carry any warnings on the package to protect those who might react.

If independent scientists discover an adverse finding that might threaten their bottom line, companies like Monsanto enlist a veritable army of supporters to drum up opposition—often using unscientific excuses that are repeated so often that they appear to be facts.

Two gene-editing companies whose stocks plummeted after the Nature Methods article came out quickly mounted their attack. But according to GMWatch.org, “the findings reported in the article, along with other recent research papers that also report unintended effects of CRISPR gene editing, show that the companies are arguing on the wrong side of the science.”[14]

The main argument used by the company Intellia was that the mutations were not from the gene editing at all. They claim that “the more plausible conclusion is that the genetic differences reflect a normal level of variation between individuals in a colony.”[15] But the scientific literature does not support this conclusion, given that:

1. Most of the mutations (117 indels and 1397 SNVS) were exactly the same in the two mice. According to GMWatch.org, “This indicates a targeted and non-random process.” If it were “a normal level of variation,” as Intellia insists, there would be much greater difference between the mice.

2. Another study looked at the genomes of 36 different strains of mice. None of the point mutations that were found in the gene-edited mice were in any of these strains. Thus, they don’t appear to be naturally occurring at all.

3. In fact, the sheer number of mutations in the edited mice was higher than scientists find among natural strains.

Perhaps the most strained logic used by Intellia to attack the research was that “there is no known mechanistic basis for Cas9 to induce SNVs.” In other words, the journal should not have published research showing unpredicted changes in the DNA simply because no one yet has figured out why those changes take place.

But if these widespread mutations exist in Crispr-Cas9 edited organisms, according to Antoniou they are likely happening with all the new gene editing techniques, which haven’t yet been studied in such detail.

Real Dangers and Perceived Dangers are Both Dangerous

If we apply these lessons to GM mosquitoes, there are serious consequences. If the saliva contains a new toxin or allergen, it might elicit mild or even deadly reactions. Since there are no human clinical trials and no public health surveillance related to the mosquito, the cause of any associated health problems could go unnoticed. It would require a large-scale outbreak of a serious reaction for health authorities to even mount an investigation, let alone consider the mosquito as a potential source.

Whether or not the GM mosquito causes harm, there is another problem that the Cayman authorities have surely overlooked. Suppose a girl who is vacationing on the island has a sudden onset of a serious health issue without an apparent cause. And suppose that her parents notice that she has also been bitten by mosquitoes. Now suppose that they draw the conclusion, correctly or incorrectly, that her condition is caused by the bite of a GM mosquito and that story is picked up by the media.

It doesn’t have to be a prominent media source for it to inspire some supermarket tabloid to dream up alarming headlines about the serious threat to American tourists by deadly engineered mosquitoes. The results could be disastrous for Cayman tourism.

The Cayman government is not only gambling that GM mosquitoes are safe (which cannot be guaranteed at this point), but also that no one draws the conclusion that they got harmed from being bitten by one. Who would want to vacation on an island where a mosquito bite could lead to who knows what?

It’s the who-knows-what that is the main point here. No one knows. But now that we understand that the generic genetic engineering process that created the mosquito also creates unpredictable and potentially dangerous changes, who in their right mind would release them? Oxitec would, obviously. And they still haven’t published any research on the composition of their GM mosquito saliva.

Oxitec is also planning to release genetically engineered moths in upstate New York. The male moths, like the mosquitoes, mate with natural females and produce larvae that don’t make it to maturity. But that larvae will inevitably be deposited into cabbage, cauliflower, and broccoli. What if the genetic engineering process alters the larvae and creates a toxin or allergen? Eating that vegetable might trigger a reaction. And just like the mosquito bite, it would be hard to trace, and the perception of harm (real or unreal) could damage produce sales from regions near the moths’ release.

Oxitec is owned by Intrexon, which also owns AquaBounty—the maker of GM salmon. The research on the salmon did show indications of off-target effects, with higher amounts of a cancer promoting hormone (IGF-1) and larger allergenic potential. But the number of fish used in the study was so small that the changes were not statistically significant. On behalf of Consumers Union, Hansen wrote to the FDA, “Because FDA’s assessment is inadequate, we are particularly concerned that this salmon may pose an increased risk of severe, even life-threatening allergic reactions to sensitive individuals. Instead of approving this product, FDA should be requiring studies with data from many more engineered fish, not the tiny sample of six fish on which it currently bases its conclusions. Unfortunately, even the data from those six fish raises concerns.” The FDA did not heed Hansen’s warning and instead approved the salmon for consumption.

At this point, there are no comprehensive analyses or feeding studies on any of these Intrexon GMOs. Their release might not only affect human health, they can permanently alter the gene pool. If the salmon escape confinement into the ocean, if the surviving GM mosquitoes or moths persist, there is no technology on earth to recall them. Any side effect can be with us for generations.

Although GMO companies like to argue that GMOs with built-in sterility will not persist in the environment. Given the fact that a percentage can survive, however, their argument is deceptive. In addition, studies confirm that after several generations, genetically engineered traits in insects can fail. A recent study, for example, showed that newly introduced traits in engineered mosquitoes failed in just 25 generations.

Intrexon can’t pretend it doesn’t know about the dangers and problems with genetic engineering technology, both real and perceived. Robert Shapiro has been on their board since 2011. He was the CEO of Monsanto who arranged to fast track the release of GMOs into the food supply. Monsanto inserted the company’s attorney into the FDA, where he pioneered the policy that allows GMOs onto the market without a single adequate safety study. Since then, numerous studies have pointed to serious health impacts, all of which are ignored or attacked.

Many of us who study the research on GMOs are convinced that they contribute to rising disease rates in the US. But even if we’re wrong, no one can pretend that the GMOs have been safe for the economy. All over the world and especially in the US, consumer rejection of GMOs has exacted a heavy economic toll on food companies and agribusiness.

But even if the regulators in the Cayman Islands and Prince Edward Island are ignoring the trends, others are wising up. According to Friends of the Earth, “more than 79 grocery retailers with more than 11,000 stores have now made commitments to not sell the GMO salmon,”[18] if it gets introduced into the market. Major brands are already racing to eliminate derivatives of GM crops, even advertising on TV that their products are non-GMO. And many countries and regions that had considered Oxitec’s GM mosquitoes have said no and are opting for safer alternatives.[19] And as long new studies continue to demonstrate serious unpredicted side-effects from genetic engineering, more consumers will take the necessary precautions.

Source=http://www.huffingtonpost.com/entry/research-exposes-new-health-risks-of-genetically-modified_us_597a3cb4e4b06b305561cef3

Note=To safe space, some references are left out

Aug 6 2017

Is this TRUE …..GLYPHOSATE has effect on AUTISM ???

MIT Researcher: Glyphosate Herbicide will Cause Half of All Children to Have Autism by 2025

 Half of All Children Will Be Autistic by 2025, Warns Senior Research Scientist at MIT

By Alliance For Natural Health
anh-usa.org

Why? Evidence points to glyphosate toxicity from the overuse of Monsanto’s Roundup herbicide on our food.

For over three decades, Stephanie Seneff, PhD, has researched biology and technology, over the years publishing over 170 scholarly peer-reviewed articles. In recent years she has concentrated on the relationship between nutrition and health, tackling such topics as Alzheimer’s, autism, and cardiovascular diseases, as well as the impact of nutritional deficiencies and environmental toxins on human health.

At a [recent] conference, in a special panel discussion about GMOs, she took the audience by surprise when she declared, “At today’s rate, by 2025, one in two children will be autistic.” She noted that the side effects of autism closely mimic those of glyphosate toxicity, and presented data showing a remarkably consistent correlation between the use of Roundup on crops (and the creation of Roundup-ready GMO crop seeds) with rising rates of autism. Children with autism have biomarkers indicative of excessive glyphosate, including zinc and iron deficiency, low serum sulfate, seizures, and mitochondrial disorder.

A fellow panelist reported that after Dr. Seneff’s presentation, “All of the 70 or so people in attendance were squirming, likely because they now had serious misgivings about serving their kids, or themselves, anything with corn or soy, which are nearly all genetically modified and thus tainted with Roundup and its glyphosate.”

Dr. Seneff noted the ubiquity of glyphosate’s use. Because it is used on corn and soy, all soft drinks and candies sweetened with corn syrup and all chips and cereals that contain soy fillers have small amounts of glyphosate in them, as do our beef and poultry since cattle and chicken are fed GMO corn or soy. Wheat is often sprayed with Roundup just prior to being harvested, which means that all non-organic bread and wheat products would also be sources of glyphosate toxicity. The amount of glyphosate in each product may not be large, but the cumulative effect (especially with as much processed food as Americans eat) could be devastating. A recent study shows that pregnant women living near farms where pesticides are applied have a 60% increased risk of children having an autism spectrum disorder.

Other toxic substances may also be autism-inducing. You may recall our story on the CDC whistleblower who revealed the government’s deliberate concealment of the link between the MMR vaccine (for measles, mumps, and rubella) and a sharply increased risk of autism, particularly in African American boys. Other studies now show a link between children’s exposure to pesticides and autism. Children who live in homes with vinyl floors, which can emit phthalate chemicals, are more likely to have autism. Children whose mothers smoked were also twice as likely to have autism. Research now acknowledges that environmental contaminants such as PCBs, PBDEs, and mercury can alter brain neuron functioning even before a child is born.

This month, the USDA released a study finding that although there were detectable levels of pesticide residue in more than half of food tested by the agency, 99% of samples taken were found to be within levels the government deems safe, and 40% were found to have no detectable trace of pesticides at all. The USDA added, however, that due to “cost concerns,” it did not test for residues of glyphosate.Let’s repeat that:they never tested for the active ingredient in the most widely used herbicide in the world. “Cost concerns”? How absurd—unless they mean it will cost them too much in terms of the special relationship between the USDA and Monsanto. You may recall the revolving door between Monsanto and the federal government, with agency officials becoming high-paying executives—and vice versa! Money, power, prestige: it’s all there. Monsanto and the USDA love to scratch each others’ backs. Clearly this omission was purposeful.

In addition, as we have previously reported, the number of adverse reactions from vaccines can be correlated as well with autism, though Seneff says it doesn’t correlate quite as closely as with Roundup. The same correlations between applications of glyphosate and autism show up in deaths from senility.

Of course, autism is a complex problem with many potential causes. Dr. Seneff’s data, however, is particularly important considering how close the correlation is—and because it is coming from a scientist with impeccable credentials. Earlier this year, she spoke at the Autism One conference and presented many of the same facts; that presentation is available on YouTube.

Monsanto claims that Roundup is harmless to humans. Bacteria, fungi, algae, parasites, and plants use a seven-step metabolic route known as the shikimate pathway for the biosynthesis of aromatic amino acids; glyphosate inhibits this pathway, causing the plant to die, which is why it’s so effective as an herbicide. Monsanto says humans don’t have this shikimate pathway, so it’s perfectly safe.

Dr. Seneff points out, however, that our gut bacteria do have this pathway, and that’s crucial because these bacteria supply our body with crucial amino acids. Roundup thus kills beneficial gut bacteria, allowing pathogens to grow; interferes with the synthesis of amino acids including methionine, which leads to shortages in critical neurotransmitters and folate; chelates (removes) important minerals like iron, cobalt and manganese; and much more.

Even worse, she notes, additional chemicals in Roundup are untested because they’re classified as“inert,” yet according to a 2014 study in BioMed Research International, these chemicals are capable of amplifying the toxic effects of Roundup hundreds of times over.

Glyphosate is present in unusually high quantities in the breast milk of American mothers, at anywhere from 760 to 1,600 times the allowable limits in European drinking water. Urine testing shows Americans have ten times the glyphosate accumulation as Europeans.

“In my view, the situation is almost beyond repair,” Dr. Seneff said after her presentation. “We need to do something drastic.”

 

Source=http://healthimpactnews.com/2014/mit-researcher-glyphosate-herbicide-will-cause-half-of-all-children-to-have-autism-by-2025/Source

 

Aug 6, 2017

 

SFFF Comments=We welcome your comments on this report  urgently

Roundup Must Carry Cancer Warning Label, Judge Decrees

In March 2015, the International Agency for Research on Cancer (IARC), a research arm of the World Health Organization (WHO), reclassified glyphosate as a “probable carcinogen” (Class 2A).1,2

The decision was based on “limited evidence” showing the weed killer can cause non-Hodgkin’s lymphoma and lung cancer in humans, along with “convincing evidence” linking it to cancer in animals.

The IARC is considered the global gold standard for carcinogenicity studies, so its determination was of considerable importance. It’s also one of the five research agencies from which the Office of Environmental Health Hazard Assessment (OEHHA) — the California agency of environmental hazards — gets its reports to declare carcinogens under Prop 65.

Monsanto has vigorously pursued a retraction of the IARC’s damning report,3 to prevent California from pursuing a cancer warning on Roundup and other, newer weed killers in the pipeline, designed for use on the company’s latest genetically engineered (GE) crops.

Monsanto Forced to Put Cancer Warning on Roundup

Their efforts have so far failed, and Fresno County Superior Court Judge Kristi Kapetan recently struck another nail in the company’s coffin, striking down Monsanto’s attempt to overturn California’s 2015 ruling to require Prop 65 warnings on glyphosate.4,5,6

While Kapetan has yet to issue a formal decision on the matter, Monsanto says it will challenge the ruling, if upheld. As reported by LA Progressive:7

“California would be the first state to order this level of labeling if this decision by the California Carcinogen Identification Committee is sustained by further court action.

Monsanto previously sued the nation’s foremost agricultural producing state by filing court motions to the effect that California’s carcinogen committee … had illegally based their decision for mandatorily requiring the warnings on ‘erroneous’ findings by an international health organization …

Trenton Norris, Monsanto’s lawyer, argued in court Friday that the labels would result in irreparable and immediate negative fiscal effect for Monsanto, because millions of consumers [would] stop buying Roundup because of the labels.”

Roundup isn’t the only weed killer that would have to bear the Prop 65 warning label. Glyphosate is also found in Ortho Groundclear, KleenUp, Aquamaster, Sharpshooter, StartUp,Touchdown, Total Traxion, Vector and Vantage Plus Max II and others.

In March 2015, the International Agency for Research on Cancer (IARC), a research arm of the World Health Organization (WHO), reclassified glyphosate as a “probable carcinogen” (Class 2A).1,2

The decision was based on “limited evidence” showing the weed killer can cause non-Hodgkin’s lymphoma and lung cancer in humans, along with “convincing evidence” linking it to cancer in animals.

The IARC is considered the global gold standard for carcinogenicity studies, so its determination was of considerable importance. It’s also one of the five research agencies from which the Office of Environmental Health Hazard Assessment (OEHHA) — the California agency of environmental hazards — gets its reports to declare carcinogens under Prop 65.

Monsanto has vigorously pursued a retraction of the IARC’s damning report,3 to prevent California from pursuing a cancer warning on Roundup and other, newer weed killers in the pipeline, designed for use on the company’s latest genetically engineered (GE) crops.

Source Dr Mercola

For more on this please visit.http://articles.mercola.com/sites/articles/archive/2017/02/14/monsantos-roundup-cancer-warning-label.aspx?utm_source

Feb 14, 2017

SA to import GM maize for first time from US

SOUTH AFRICA – The government has approved imports of genetically modified maize from the US for the first time as the country seeks to bring in the grain after its worst drought since records began 104 years ago.

The country will allow the import of both white and yellow GM maize from the US, said Dirk Kok, a spokesperson for the secretariat of the Pretoria-based South African Cereals and Oilseeds and Trade Association, in an interview on Monday.

“The door is open to imports from the US” said Kok, whose organisation represents grain and oil seed traders. Local “prices will come down”.

South Africa has become a net importer of maize for the first time since 2008 after the drought slashed this year’s harvest by about a quarter to 7.97 million tonnes, the smallest crop since 2006.

That’s pushed up prices on Johannesburg’s South African Futures Exchange with white maize, used in South Africa to make the country’s staple food of maize meal, surging 80% since the end of 2014 to R3 855 a metric tonnes.

Yellow maize, used for animal feed, has jumped 45% in the same period to R3 147 a ton.

The decision “is critical,” Wandile Sihlobo, the head of economic and agribusiness intelligence at the Agricultural Business Chamber, said by phone from Pretoria.

“We are going to see a more strong correlation between the yellow maize price and the US price. The reaction of the South African farmers is going to be interesting.”

By the end of April South Africa may import 300 000 tonnes of GM white maize from the US and 500 000 tonnes of yellow maize, he said.

South Africa imported 555 241 tonnes of white maize between May 1 and November 25, or 65% of the imports forecast for the season ending April 30, according to the Agricultural Business Chamber. Almost all of that came from Mexico.

“This will allow US corn, both white and yellow, to ship into South Africa fairly easily,” Cary Sifferath, senior director of Washington-based US Grains Council, said by phone.

“In the short term, as they wait for harvest in late April to May, there could be some need for some additional white corn imports.” – Bloomberg

Decmber 6, 2016; http://www.fin24.com/Companies/Agribusiness/sa-to-import-gm-maize-for-first-time-from-us-20161206

EU PROLONGS GLYPHOSATE LICENCE BY 18 MONTHS

A new study has found that low-dose and long-term exposure to the  weed killer Roundup causes liver disease in female rats.

However, the company,Monsanto has reacted, saying that the study used “flawed data” from 2012.

The Roundup herbicide contains controversial ingredient glyphosate, which is now one of the world’s most popular weed killers. The use of glyphosate has triggered strong reactions in the EU amid fears the product is carcinogenic.

In late June, the European Commission decided to extend the authorisation licence for glyphosate by 18 months, until the European Chemicals Agency (ECHA) gives an opinion on the substance. The ECHA’s opinion is expected in June or September this year.

Commission prolongs glyphosate licence by 18 months

The European Commission has decided to extend the licence for glyphosate by 18 months, after member states failed to achieve a qualified majority in favour or against the executive’s proposal.

EurActiv.com

 

Liver disease

A new study published this week (9 January) in Scientific Reports found that low levels of exposure to the weed killer Roundup over an extended period causes liver disease in rats.

The study focused on Roundup and not glyphosate alone and stated that it was not possible “to attribute the toxicity of the whole agricultural herbicide formulation to a given component”.

“Future studies involving the administration of glyphosate alone would shed light on this issue,” the study concluded.

Female rats were administered with an extremely low dose of Roundup weed killer over a two-year period and found to suffer from non-alcoholic fatty liver disease (NAFLD). The dose selected was below what people are commonly exposed to in the everyday environment and 75,000 times below what is permitted by EU regulators.

For a two-year period, female rats were administered a dose of Roundup, approximately 75,000 times below what is permitted by EU regulators for human exposure, and were found to suffer from non-alcoholic fatty liver disease.

Researchers pointed out that it was the first time that a causative link between consumption of Roundup at a “real world” environmental dose and a serious disease condition was identified.

Dr. Michael Antoniou, an author of the study, stressed that the findings were “worrying” and called EU policy-makers to reconsider the safety evaluation of glyphosate-based herbicides.

According to Antoniou, fatty liver disease occurs in at least one in five of the general population, and in the vast majority of people with type 2 diabetes.

source=euractiv.com

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