'Genetically Engineered Organisms, Are They  Safe?' Leading experts representing  both sides of the issue shed light on the controversy
 By Léo Azambuja
 The presence of Genetically Engineered  (GE) crops on Molokai has been a controversial topic for some time. Earlier this  year Monsanto, the leading GE company worldwide, expanded its operations on  Molokai to include 1,650 acres, raising concerns amongst those who believe GE  farming might irreversibly affect the environment. But there are also those who  believe GE crops are beneficial and do not pose environmental or health  threats.
 The Molokai Dispatch has engaged leading  scientists and professionals in health and agricultural fields to weigh in on  the GE farming issues which could affect Molokai. To be fair, a set of six  questions was sent to opposite sides of the opinion field. Here, we present the  first two sets of questions, and their respective answers. In the next issue,  the Dispatch will publish the remaining three sets of questions.
 Challenging the benefits of GE crops are:  Bill Freese, a Science Policy Analyst at the Center for Food Service in  Washington D.C.; and Dr. Lorrin Pang, who works for the Hawaii State Department  of Health as a Maui District officer. 
 Representing the defense of GE crops are:  Harold Keyser, PhD, a Maui County Administrator for the College of Tropical  Agriculture & Human Resources at the University of Hawaii; and Sally Irwin,  a PhD in genetics, who is an associate professor at Maui Community  College.
 Please be aware that the professionals  participating in this forum do not, in any way, represent the views of their  respective employers or subordinates.
  
 Is there available scientific  evidence suggesting or proving that GE farming could adversely affect the  surrounding environment? 
 Harold Keyser, Ph.D.:  
 The short answer is clearly no. In fact,  just the opposite has been found. Large scale scientific studies with different  biotech crops have shown that their use can significantly reduce the amount of  pesticide that farmers use compared to non-biotech crops; well documented in the  scientific literature are reports showing 40% reduction over 3 years in the  United Kingdom, reduction of 46 million pounds in the US in a single year, and  80% less pesticide use on rice over a two year period in China.
 Improved soil conservation is another  environmental benefit from the adoption of biotech crops. Grower surveys and  expert polls strongly indicate that the adoption of herbicide-resistant crops  correlated positively with increase in no-till acreage since 1996, the year when  herbicide-resistant crops were first planted on a commercial scale. 
 No-till and minimum tillage practices  enhance soil quality through reduction in loss of soil organic matter, reduced  loss of CO2 (a greenhouse gas), reduced soil erosion, and increased water  infiltration. In 2006, 16 million acres of corn, and 33 million acres of soybean  in the US (representing 20% and 44%, respectively, of the total crop) were  planted by no-till. 
 There is a belief among some opponents of  genetic engineering that the new biotech crops might cross-pollinate with  related (genetically compatible) weeds, possibly resulting in “superweeds” that  become more difficult to control. One concern is that pollen transfer from  glyphosate-resistant crops to related weeds can confer resistance to glyphosate.  While the chance of this happening, though extremely small, is not  inconceivable, there are other classes of herbicides which could be used to  control such a plant. 
 In Hawaii, the main biotech crops are  papaya and corn. Neither has led to development of “superweeds;” indeed, the  nearest relative for corn to successfully transfer pollen to is in Mexico.  
 In assessing the evidence on risks versus  benefits to the environment of GE farming, the benefits are clear and the risks,  so far, remain theoretical.
 Dr. Lorrin  Pang:
 We do know of contamination and recall of  our food supply (for example Starlink corn) with GE products not intended for  human consumption. Last year US commercial rice (long grain) was found to be  contaminated with unapproved experimental GE rice, which was planted under  “restricted” conditions from 1998-2001, resulting in a massive, expensive recall  and ongoing litigation. 
 There are laboratory studies which show  that the GE mutations can be transferred from GE plants to soil microbes. We are  learning that microbes (especially viruses) are especially efficient at  transferring genes (including GE mutations) among the different species of  plants that it infects. 
 Finally, there are reports of “superweeds”  which cannot be killed by use of Roundup and require more potent, toxic  herbicides. In the field of medicine we see that germs become resistant when  antibiotics are overused and abused. The same is true in the field of insects  and insecticides. It surely occurs for plants and herbicides. But the difference  with GE Round-Up Ready plants is that they are given the mutations to resist  Round-Up. Do superweeds make resistance on their own do they simply “steal” the  protective gene from the GE crops?
 In medicine we have seen how easy it is to  spread and share genes. As we observe the occurrence of “theoretically  impossible events”, we should be humbled by how little we know or can predict  with our current level of genomic knowledge in a single organism, let alone in  ecology. 
 Bill Freese:  
 Four of every 5 acres of GE crops  worldwide are herbicide-tolerant, which allows farmers to indiscriminately spray  a chemical weedkiller “over-the-top” of the crop to kill nearby weeds. The vast  majority are Monsanto’s Roundup Ready varieties, resistant to Monsanto’s Roundup  herbicide (aka glyphosate).
 Herbicide-tolerant crops encourage  large-scale, chemical-intensive farming. Glyphosate use has climbed ten-fold  since the first Roundup Ready crop was introduced in 1995. USDA data show  increased use of other nasty weedkillers, too, like atrazine and 2,4-D (a  component of the infamous Agent Orange). 
 Increased chemical use has fostered an  epidemic of herbicide-resistant weeds, just as overuse of antibiotics spawns  resistant bacteria. Resistant horseweed infests over 1.5 million acres in  Tennessee, and resistant pigweed in Georgia survives 12 times the normal dose of  glyphosate. Many farmers now plow to remove resistant weeds, increasing soil  erosion.
 GE crops also reduce biodiversity. A 2003  study by the British government found lower populations of bees and butterflies  in test plots of GE beets and canola. Commercial-scale plantings would threaten  the survival of birds by reducing the weed seeds they feed on. Roundup is toxic  to some amphibians, and may be implicated in declining frog populations. Recent  research shows that the toxin produced in GE corn may harm aquatic food webs.  
  
 Is GE produce required to  carry identifying labels? Is there any scientific evidence suggesting or proving  that GE produce could adversely affect humans? What is your stance on the  current level of government regulation of the GE  industry?
 Dr. Lorrin  Pang:
 The FDA once ruled that no studies are  needed because the GE foods are “equivalent” to non-GE foods. This is an opinion  and not data based. 
 The FDA opinion goes against that of the  National Academy of Science (NAS) which provides a graph showing that GE foods  have a higher risk of unintended health effects. There is a caveat by the NAS  that unintended health effects are not necessarily “bad” – but if I was in the  best of health I would not want to risk new unintended effects 
 Sometimes the FDA gives a “grandfather  clause” that GE foods have been used for decades and so they probably are safe.  Long term exposures to new products require long term studies for chronic  toxicities – to include cancer. Think of the decades it took us to figure out  smoking caused cancers.
 Finally, like products which MIGHT have  long term, cumulative, irreversible health effects (say cancer) we especially  need to follow the precautionary principle. This principle requires that  commercial products have their risks studied prior to marketing. Risks do not  have to be zero but must be known and the public informed as part of labeling.  If the risks are truly zero (as verified under large, long term, post marketing  studies) I would like to see the data and then MIGHT consider removing labeling  and warnings.
 Sally V. Irwin  Ph.D.:
 The U.S. Food and Drug Administration (FDA) has a labeling  policy that requires biotech foods to be labeled if the product is significantly  changed nutritionally or uses material from a potential allergen. In other  words, if a biotech product is nutritionally the same as a non-biotech product,  there is no requirement for labels. The American Medical Association Council on  Scientific Affairs supported this policy. 
 However, if a biotech food product introduces a protein  from a source that commonly poses an allergy risk, then it must be labeled under  the current FDA labeling policy. Today, the majority of biotech products in the  marketplace are not labeled as such since they are nutritionally equivalent and  are not derived from known allergens.
 What many people don’t understand is that all the food we  eat are constantly changing genetically, sometimes intentionally by breeding and  selection techniques, chemical or irradiation treatments to cause mutagenesis,  spontaneously through mutation or insertion of genes from other organisms (i.e.  viruses), or through bioengineering techniques. The only food that is being  tested and regulated for ill effects due to genetic changes is the bioengineered  food. 
 To date there has not been one documented case where a  bioengineered food has caused a health problem in humans. 
 Scientists around the world have reached a  remarkable degree of agreement that biotech-derived foods are safe to eat. In  fact, some international food safety organizations have concluded that because  of the strict regulatory oversight of biotech foods, they are probably even  safer than conventional plants and foods
 Bill  Freese:
 The health risks of genetic engineering  arise from the new compound(s) intentionally introduced into the crop, and the  unpredictable effects of genetic engineering itself.
 GE corn with “built-in” insecticides was  grown on 45 million acres this year in the U.S., and poses the risk of food  allergies.
 One such GE corn variety approved only for  animal feed use massively contaminated the food supply in 2000, resulting in  recall of over 300 food products and hundreds of reported allergic reactions,  some of them life-threatening.
 A British study found that the  herbicide-resistance gene in GE soybeans transferred to gut bacteria in people  who ate GE soy products, showing that the same could happen with antibiotic  resistance genes.
 The GE Flavr-Savr tomato caused gastric  lesions in rats – findings that were dismissed, but never adequately explained,  by the FDA. Hungarian scientist Arpad Pusztai found hyperplastic intestinal cell  growth in rats fed GE potatoes. A short 90-day feeding study with a Monsanto GE  corn variety found signs of liver and kidney damage.
 U.S. government “regulation” of  genetically engineered (GE) crops and foods is largely a sham exercise to  reassure the American public rather than ensure that GE crops are safe for human  health and the environment. 
 Experimental GE crops grown in field  trials have contaminated the commercial food supply numerous times under the  U.S. Dept. of Agriculture’s watch. Evidence that insecticide-producing corn may  cause food allergies, liver or kidney damage has been ignored by the  Environmental Protection Agency, while the Food and Drug Administration lets  biotech companies determine whether their GE crops are safe.
 Biotechnology companies – particularly  Monsanto – “wrote the book” on the rules that govern them during the first Bush  Administration. 
 FDA scientists opposed this policy of  “self-policing,” and instead recommended mandatory toxicology studies, tests for  genotoxic effects, and even “limited studies in humans” for new GE crops. They  emphasized that genetic engineering could cause hazardous unintended effects not  found with traditional breeding. These scientific concerns were overruled by  administrative superiors at the FDA and White House, resulting in today’s  “voluntary consultation process,” which rests on the fiction that GE crops are  “substantially equivalent” to traditionally-bred crops.
 Under voluntary consultation, biotech  companies, not FDA, are responsible for the safety of GE crops. Companies decide  which tests to perform, how to conduct them, which data to share or not share  with FDA, and even whether to consult with FDA at all.
 Independent experts, including the  National Academy of Sciences, have repeatedly criticized government regulation  and biotech company health and safety testing as grossly inadequate. 
 Harold Keyser,  Ph.D.:
 The U.S. government has a coordinated,  risk-based system to ensure new biotechnology products are safe for the  environment and human and animal health. 
 Established in 1986, the Coordinated  Framework for Regulation of Biotechnology describes the federal system for  evaluating products developed using modern biotechnology. The Coordinated  Framework is based upon health and safety laws developed to address specific  products and is carried out by the USDA, EPA and FDA prior to commercial release  for genetically modified (GM) crops. These pre-market tests have consistently  found that the new proteins in GM crops show no similarity to known toxins or  allergens; they are present in very low levels; they are easily and rapidly  digested by humans and animals; and they have shown no harmful effects to  animals when fed at very high levels. As a result, the food and feed products  from GM crops have a perfect safety record with not one verified incident of  harm after growing and consuming them on a large scale for over a decade.  
 In 2004, the National Academy of Sciences’  comprehensive report on this issue stated the following: “To date, no adverse  health effects attributed to genetic engineering have been documented in the  human population.” Similar conclusions have been reached by the American Medical  Association, World Health Organization, and the American Dietetic  Association.
 The USDA is responsible for ensuring  compliance with regulations of biotech crops. Depending on the type of crop  being tested, a site may be inspected by USDA up to seven times to ensure that  the requirements are carefully followed. In Hawaii during 2004, they conducted  79 inspections of permitted field tests and 148 inspections of field tests  approved through the notification process. 
 Detractors who say this industry is not  sufficiently regulated have not done their homework.
 9 Nov 2007
 http://www.themolokaidispatch.com/node/1289