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Not to be confused with glufosinate.
IUPAC name
Other names
2-[(phosphonomethyl)amino]acetic acid
1071-83-6 YesY
38641-94-0 (isopropylammmonium salt)
70393-85-0 (sesquisodium salt)
81591-81-3 (trimethylsulfonium salt)
ChEBI CHEBI:27744 YesY
ChemSpider 3376 YesY
EC-number 213-997-4
Jmol-3D images Image
KEGG C01705 YesY
PubChem 3496
RTECS number MC1075000
UNII 4632WW1X5A YesY
Molar mass 169.07 g·mol−1
Appearance white crystalline powder
Density 1.704 (20 °C)
Melting point 184.5 °C (364.1 °F; 457.6 K)
Boiling point decomposes at 187 °C (369 °F; 460 K)
1.01 g/100 mL (20 °C)
log P −2.8
Acidity (pKa) <2, 2.6, 5.6, 10.6
GHS pictograms Eye Dam. 1Aquatic Chronic 2
GHS signal word DANGER
H318, H411
P273, P280, P305+351+338, P310, P501
EU Index 607-315-00-8
EU classification Irritant (Xi)
Dangerous for the environment (N)
R-phrases R41, R51/53
S-phrases (S2), S26, S39, S61
Flash point Non-flammable
Except where noted otherwise, data is given for materials in their standard state (at 25 °C (77 °F), 100 kPa)
 YesY verify (what isYesY/N?)
Infobox references

Glyphosate (N-(phosphonomethyl)glycine) is a broad-spectrum systemic herbicide used to kill weeds, especially annual broadleaf weeds and grasses known to compete with commercial crops grown around the globe. It was discovered to be a herbicide by Monsanto chemist John E. Franz in 1970.[3] Monsanto brought it to market in the 1970s under the trade name Roundup and Monsanto's last commercially relevant United States patent expired in 2000.

Glyphosate was quickly adopted by farmers, even more so when Monsanto introduced glyphosate-resistant crops, enabling farmers to kill weeds without killing their crops. In 2007, glyphosate was the most used herbicide in the United States agricultural sector, with 180 to 185 million pounds (82,000 to 84,000 tonnes) applied, and the second-most used in home and garden market where users applied 5 to 8 million pounds (2,300 to 3,600 tonnes); in addition, industry, commerce, and government applied 13 to 15 million pounds (5,900 to 6,800 tonnes).[4] With its heavy use in agriculture, weed resistance to glyphosate is a growing problem. While glyphosate and formulations such as Roundup have been approved by regulatory bodies worldwide and are widely used, concerns about their effects on humans and the environment persist.

Glyphosate's mode of action is to inhibit an enzyme involved in the synthesis of the aromatic amino acids: tyrosine, tryptophan, and phenylalanine. It is absorbed through foliage and translocated to growing points. Because of this mode of action, it is only effective on actively growing plants; it is not effective as a pre-emergence herbicide.

Some crops have been genetically engineered to be resistant to glyphosate (i.e., Roundup Ready, also created by Monsanto Company). Such crops allow farmers to use glyphosate as a postemergence herbicide against both broadleaf and cereal weeds, but the development of similar resistance in some weed species is emerging as a costly problem. Roundup Ready soybean was the first Roundup Ready crop.

Regulatory and scholarly reviews of the toxicity of glyphosate found it to be relatively safe as an herbicide, until a meta-analysis published in 2014 identified an increased risk of non-Hodgkin lymphoma in workers exposed to glyphosate formulations.[5] However, the same data had been analyzed by the German Institute for Risk Assessment in a report also published in 2014, which found that "the available data is contradictory and far from being convincing" with regard to correlations between exposure to glyphosate formulations and risk of various cancers including NHL.[6]:Volume 1, p64-66 In March 2015 the World Health Organization's International Agency for Research on Cancer published a summary of its forthcoming monograph on glyphosate, and classified glyphosate as "probably carcinogenic in humans" (category 2A) based on epidemiological studies, animal studies, and in vitro studies; it noted that there was "limited evidence" of carcinogenicity in humans for non-Hodgkin lymphoma.[7][8][9]


Glyphosate was first synthesized in 1950 by Swiss chemist Henry Martin, who worked for the Swiss company Cilag. The work was never published.[10]:1 In a case of parallel invention, glyphosate was independently discovered at Monsanto in 1970. Monsanto chemists had synthesized about 100 analogs of aminomethylphosphonic acid as potential water-softening agents. Two were found to have weak herbicidal activity, and John E. Franz, a chemist at Monsanto, was asked to try to make analogs with stronger herbicidal activity. Glyphosate was the third analog he made.[10]:1–2[11]

Glyphosate has been called by experts in herbicides "virtually ideal" due to its broad spectrum and low toxicity to animal life compared with other herbicides.[12][13][14][15] Franz received the National Medal of Technology in 1987[16] and the Perkin Medal for Applied Chemistry[17] in 1990 for his discoveries. Franz was inducted into the National Inventor's Hall of Fame in 2007.[18]


Glyphosate synthesis from chloroacetic acid

Glyphosate is an aminophosphonic analogue of the natural amino acid glycine, and the name is a contraction of gly(cine) phos(phon)ate. The molecule has several dissociable hydrogens, especially the first hydrogen of the phosphate group. The molecule tends to exist as a zwitterion where a phosphonic hydrogen dissociates and joins the amine group. Glyphosate is soluble in water to 12 g/l at room temperature.

Glyphosate synthesis from dimethyl phosphite

The main deactivation path is hydrolysis to aminomethylphosphonic acid (AMPA).[19]


Glyphosate kills plants by interfering with the synthesis of the aromatic amino acids phenylalanine, tyrosine, and tryptophan. It does this by inhibiting the enzyme 5-enolpyruvylshikimate-3-phosphate synthase (EPSPS), which catalyzes the reaction of shikimate-3-phosphate (S3P) and phosphoenolpyruvate to form 5-enolpyruvyl-shikimate-3-phosphate (ESP).[20]


ESP is subsequently dephosphorylated to chorismate, an essential precursor for the amino acids mentioned above.[21] These amino acids are used in protein synthesis and to produce secondary metabolites such as folates, ubiquinones, and naphthoquinone.

X-ray crystallographic studies of glyphosate and EPSPS show that glyphosate functions by occupying the binding site of the phosphoenolpyruvate, mimicking an intermediate state of the ternary enzyme substrates complex.[22][23]

The commercially important enzyme that glyphosate inhibits, EPSPS, is found only in plants and micro-organisms. EPSPS is not present in animals, which instead obtain aromatic amino acids from their diets.[24]

Glyphosate is absorbed through foliage. Because of this mode of action, it is only effective on actively growing plants; it is not effective in preventing seeds from germinating.

Environmental fate[edit]

Glyphosate adsorbs strongly to soil and is not expected to move vertically below the six-inch soil layer; residues are expected to be immobile in soil. Glyphosate is readily degraded by soil microbes to aminomethylphosphonic acid (AMPA) and carbon dioxide. Glyphosate and AMPA are not likely to move to ground water due to their strong adsorptive characteristics. However, glyphosate does have the potential to contaminate surface waters due to its aquatic use patterns and through erosion, as it adsorbs to soil particles suspended in runoff. If glyphosate reaches surface water, it would not be broken down readily by water or sunlight.[25]

The half-life of glyphosate in soil ranges between 2 and 197 days; a typical field half-life of 47 days has been suggested. Soil and climate conditions affect glyphosate's persistence in soil. The median half-life of glyphosate in water varies from a few to 91 days.[26]

According to the National Pesticide Information Center fact sheet, glyphosate is not included in compounds tested for by the Food and Drug Administration's Pesticide Residue Monitoring Program, nor in the United States Department of Agriculture's Pesticide Data Program. However, a field test showed that lettuce, carrots, and barley contained glyphosate residues up to one year after the soil was treated with 3.71 lb of glyphosate per acre (4.15 kg per hectare).[26]


Glyphosate used as an alternative to mowing in an apple orchard in Ciardes, Italy

Glyphosate is effective in killing a wide variety of plants, including grasses and broadleaf and woody plants. It has a relatively small effect on some clover species.[27] By volume, it is one of the most widely used herbicides.[26] It is commonly used for agriculture, horticulture, viticulture, and silviculture purposes, as well as garden maintenance (including home use).[26][28]

In many cities, glyphosate is sprayed along the sidewalks and streets, as well as crevices in between pavement where weeds often grow. However, up to 24% of glyphosate applied to hard surfaces can be run off by water.[29] Glyphosate contamination of surface water is attributed to urban and agricultural use.[30] Glyphosate is used to clear railroad tracks and get rid of unwanted aquatic vegetation.[31]

In addition to its use as an herbicide, glyphosate is also used for crop desiccation (siccation) to increase harvest yield[31] and, as a result of desiccation, to increase sucrose concentration in sugarcane before harvest.[32]

Formulations and tradenames[edit]

Glyphosate is marketed in the United States and worldwide by many agrochemical companies, in different solution strengths and with various adjuvants, under dozens of tradenames.[33][34][35][36] As of 2013, it was the world's largest-selling herbicide, and Chinese manufacturers collectively are the world's largest producers of glyphosate and its precursors.[37]

Manufacturers include Bayer, Dow AgroSciences, Du Pont, Cenex/Land O’Lakes, Helena, Monsanto, Platte, Riverside/Terra, and Zeneca.[36]

Glyphosate is an acid molecule, so it is formulated as a salt for packaging and handling. Various salt formulations include isopropylamine, diammonium, monoammonium, or potassium as the counterion. Some brands include more than one salt. Some companies report their product as acid equivalent (ae) of glyphosate acid, or some report it as active ingredient (ai) of glyphosate plus the salt, and others report both. To compare performance of different formulations, knowledge of how the products were formulated is needed. Since the salt does not contribute to weed control and different salts have different weights, the acid equivalent is a more accurate method of expressing and comparing concentrations.[38] Adjuvant loading refers to the amount of adjuvant[39][40] already added to the glyphosate product. Fully loaded products contain all the necessary adjuvants, including surfactant; some contain no adjuvant system, while other products contain only a limited amount of adjuvant (minimal or partial loading) and additional surfactants must be added to the spray tank before application.[38] As of 2000 (just before Monsanto's patent on glyphosate expired), over 400 commercial adjuvants from over 34 different companies were available for use in commercial agriculture.[41][42]

Products are supplied most commonly in formulations of 120, 240, 360, 480, and 680 g/l of active ingredient. The most common formulation in agriculture is 360 g/l, either alone or with added cationic surfactants.

For 360 g/l formulations, European regulations allow applications of up to 12 l/ha for control of perennial weeds such as couch grass. More commonly, rates of 3 l/ha are practiced for control of annual weeds between crops.[43]


Monsanto's Roundup is the earliest formulation of glyphosate.

Monsanto developed and patented the use of glyphosate to kill weeds in the 1970s, and has marketed it as Roundup since 1973. It retained exclusive rights in the United States until its patent expired in September, 2000.

As of 2009, sales of these herbicide products represented about 10% of Monsanto's revenue due to competition from other producers of other glyphosate-based herbicides;[44] their Roundup products (which include GM seeds) represented about half of Monsanto's gross margin.[45]

The active ingredient of the Monsanto herbicides is the isopropylamine salt of glyphosate. Another important ingredient in some formulations is the surfactant polyethoxylated tallow amine.

Monsanto also produces seeds which grow into plants genetically engineered to be tolerant to glyphosate. The genes contained in these seeds are patented. Such crops allow farmers to use glyphosate as a postemergence herbicide against most broadleaf and cereal weeds. Soy was the first glyphosate-resistant crop.


Glyphosate is the active ingredient in herbicide formulations containing it. However, in addition to glyphosate salts, commercial formulations of glyphosate contain additives such as surfactants which vary in nature and concentration. Laboratory toxicology studies have suggested that other ingredients in combination with glyphosate may have greater toxicity than glyphosate alone.[46] Toxicologists have studied glyphosate alone, additives alone, and formulations.

Glyphosate toxicity[edit]


Human acute toxicity is dose-related. Acute fatal toxicity has been reported in deliberate overdose.[46][47] Early epidemiological studies have not found associations between long-term low-level exposure to glyphosate and any disease.[48][49][50] Neither glyphosate nor typical glyphosphate-based formulations (GBFs) pose a genotoxicity risk in humans under normal conditions of human or environmental exposures.[51]

The EPA, which last reviewed glyphosate in 1993, considers glyphosate to be noncarcinogenic and relatively low in dermal and oral acute toxicity.[25] The EPA considered a "worst case" dietary risk model of an individual eating a lifetime of food derived entirely from glyphosate-sprayed fields with residues at their maximum levels. This model indicated that no adverse health effects would be expected under such conditions.[25] As of March 2015, the EPA was in the midst of reviewing glyphosate's toxicity.[7]

The European Commission's review of the data conducted in 2002 concluded equivocal evidence existed of a relationship between glyphosate exposure during pregnancy and cardiovascular malformations; however, a review published in 2013 found the evidence "fails to support a potential risk for increased cardiovascular defects as a result of glyphosate exposure during pregnancy."[52]

A 2013 systematic review by the German Institute for Risk Assessment (BfR), conducted as part of the EFSA's review process, examined epidemiological studies, animal studies, and in vitro studies that it found valid, and found that "no classification and labelling for carcinogenicity is warranted" and recommended a carcinogen classification of 1A or 1B.[6]:Volume 1, p139, see also 34-37 It was provided to the EFSA in January 2014 and published by the EFSA in December 2014[6][53]

In March 2015, the International Agency for Research on Cancer published a summary of their forthcoming monograph on glyphosate, and classified glyphosate as "probably carcinogenic in humans" (category 2A) based on epidemiological studies, animal studies, and in vitro studies; it noted that there was "limited evidence" of carcinogenicity in humans for non-Hodgkin lymphoma.[7][9][8] The German Institute for Risk Assessment responded that the work group reviewed only a selection of what they had reviewed earlier, and argued that other studies among which the well-cited cohort study Agricultural Health Study do not support the classification.[54]

Fish and amphibians[edit]

Glyphosate is generally less persistent in water than in soil, with 12- to 60-day persistence observed in Canadian pond water, yet because glyphosate binds to soil, persistence of over a year has been observed in the sediments of ponds in Michigan and Oregon.[25] In streams, maximum glyphosate concentrations were measured immediately after treatment and dissipated rapidly.[25] According to research done in the late 1980s and early 1990 (Ecotoxicological Risk Assessment for Roundup Herbicide), glyphosate in ecological exposures studied is "practically nontoxic to slightly toxic" for amphibians and fish.[55]

In a 2013 review, mixed results were observed in nonmammalian systems. Glyphosate and GBFs tend to elicit DNA damage effects at high or toxic dose levels, but the data suggest this is due to cytotoxicity rather than genotoxicity. GBF activity is perhaps associated with the associated surfactants.[51]

Soil, microorganisms and worms[edit]

Degradation pathway of glyphosate in the ground[55]

When glyphosate comes into contact with the soil, it can be rapidly bound to soil particles and be inactivated.[25][56] Unbound glyphosate can be degraded by bacteria.[57] Glyphosate and its degradation product, AMPA, residues are considered to be much more toxicologically and environmentally benign than most of the herbicides replaced by glyphosate.[58]

In soils, half-lives vary from as little as three days at a site in Texas to 141 days at a site in Iowa.[56] In addition, the glyphosate metabolite AMPA has been found in Swedish forest soils up to two years after a glyphosate application. In this case, the persistence of AMPA was attributed to the soil being frozen for most of the year.[59] Glyphosate adsorption to soil, and later release from soil, varies depending on the kind of soil.[60][61] A 2009 study using a RoundUp formulation concluded absorption into plants delays subsequent soil degradation and can increase glyphosate persistence in soil from two to six times.[62]

Laboratory studies published in 1991 and 1992 indicated GBFs could harm beneficial insects[63] and earthworms.[64] However, the reported effect of glyphosate on earthworms has been criticized.[55] The results conflict with results from field studies where no effects were noted for the number of nematodes, mites, or springtails after treatment with Roundup at 2 kg/ha of active ingredient.[65]

Glyphosate can harm the bacterial ecology of soil and cause micronutrient deficiencies in plants.[66] Other studies found that while "recommended dosages of glyphosate did not affect growth rates", much higher dosages reduced respiration in nitrogen-fixing bacteria.[67][68] A 2012 study on the effect of Roundup (glyphosate with adjuvants) on three microorganisms used in dairy products found, while the formulation had "a microbicide effect at lower concentrations than those recommended in agriculture", glyphosate alone "at these levels has no significant effect".[69]

Additive toxicity[edit]

Glyphosate formulations may contain a number of adjuvants, the identity of which is considered a trade secret and not disclosed by government regulators. In the United States, the Federal Insecticide, Fungicide, and Rodenticide Act requires that all pesticides (including herbicides) be evaluated by the EPA prior to sale, including product’s chemistry, environmental fate, residue chemistry, dietary and nondietary hazards to humans, and hazards to domestic animals and nontarget organisms[70] These evaluations are performed for each active ingredient, each inert ingredient, and for the final product formulation. Additional evaluations are performed by the FDA to set permitted residue levels in food for pesticide products used on food crops.[71]


Surfactants lower the surface tension (or interfacial tension) between two liquids or between a liquid and a solid. They may act as detergents, wetting agents, emulsifiers, foaming agents, and dispersants. As agricultural spray adjuvants, they may be included in a formulation sold to the consumer (in can), or may be bought separately and mixed on site (tank mix).

Polyethoxylated tallow amine (POEA) is part of the original Roundup formulation. Registration data in New Zealand showed Roundup contained 18% POEA. POEA is a surfactant that enhances the activity of herbicides such as glyphosate. The role of a surfactant in a herbicide product is to improve wetting of the surface of plants for maximum coverage and aid penetration through the plant surface. A review of the literature provided to the EPA in 1997 found POEA to be more toxic to fish than glyphosate.[72]

Spreader 90 is a surfactant used in tank mixes.[76] Spreader 90 contains 1,2 propanediol (also known as propylene glycol), propane 1,2,3 triol (also known as glycerol), alcohol ethoxylate, and dimethylpolysiloxane.[77][78] Of these ingredients, alcohol ethoxylates are among the widely used detergents in consumer products; commercial preparations are often mixes of homologs. Due to known toxicities to aquatic species, the Canadian recommended Federal Water Quality Guideline values are 70 µg/l.[79]

Formulation toxicity[edit]


A 2000 review concluded that "under present and expected conditions of new use, there is no potential for Roundup herbicide to pose a health risk to humans".[80] A 2002 review by the European Union reached the same conclusion.[81]

Data from the California Environmental Protection Agency's Pesticide Illness Surveillance Program, which also tracks other agricultural chemicals, show glyphosate-related incidents are some of the most common.[82][83] However, incident counts alone do not take into account the number of people exposed and the severity of symptoms associated with each incident.[83] For example, if hospitalization were used as a measure of the severity of incidents, then glyphosate would be considered relatively safe; over a 13-year period in California, none of the 515 reported hospitalizations was attributed to glyphosate.[83]

Dermal exposure to ready-to-use glyphosate formulations can cause irritation, and photocontact dermatitis has been occasionally reported. These effects are probably due to the preservative benzisothiazolin-3-one. Severe skin burns are very rare.[46] Inhalation is a minor route of exposure, but spray mist may cause oral or nasal discomfort, an unpleasant taste in the mouth, or tingling and irritation in the throat. Eye exposure may lead to mild conjunctivitis. Superficial corneal injury is possible if irrigation is delayed or inadequate.[46]

Deliberate ingestion of Roundup in quantities ranging from 85 to 200 ml (of 41% solution) has resulted in death within hours of ingestion, although it has also been ingested in quantities as large as 500 ml with only mild or moderate symptoms.[84] A reasonable correlation is seen between the amount of Roundup ingested and the likelihood of serious systemic sequelae or death. Ingestion of more than 85 ml of the concentrated formulation is likely to cause significant toxicity in adults. Corrosive effects – mouth, throat and epigastric pain and dysphagia – are common. Renal and hepatic impairment are also frequent, and usually reflect reduced organ perfusion. Respiratory distress, impaired consciousness, pulmonary edema, infiltration on chest X-ray, shock, arrhythmias, renal failure requiring haemodialysis, metabolic acidosis, and hyperkalaemia may occur in severe cases. Bradycardia and ventricular arrhythmias often present prior to death.

A 2012 meta-analysis of all epidemiological studies of exposure to glyphosate formulations found no correlation with any kind of cancer.[85] The 2013 systematic review by the German Institute for Risk Assessment of epidemiological studies of workers who use pesticides, exposed to glyphosate formulations found no significant risk, stating that "the available data is contradictory and far from being convincing".[6]:Volume 1, p64-66 However, a 2014 meta-analysis of the same studies found a correlation between occupational exposure to glyphosate formulations and increased risk of B cell lymphoma, the most common kind of non-Hodgkin lymphoma (NHL). Workers exposed to glyphosate were about twice as likely to get B cell lymphoma.[5] Overall, around 2% of adults (including workers) are diagnosed with NHL at some point during their lifetime.[86]

Endocrine disruption[edit]

In a study of rats and mice fed diets of containing 0%, 0.3125%, 0.625%, 1.25%, 2.5%, or 5.0% glyphosate for 13 weeks, endocrine effects were observed only in rats and only at the two highest doses. Male rats at the highest dose exhibited reductions in sperm concentrations that remained within the strain's normal range. Female rats in the highest dose group experienced a slight increase in the length of the estrous cycle.[26]

Administering Roundup Transorb orally to prepubescent rats once a day for 30 days reduced testosterone production and affected testicle morphology, but did not affect levels of estradiol and corticosterone.[87]

In 2007, the EPA selected glyphosate for further screening through its Endocrine Disruptor Screening Program. Selection for this program is based on a compound's prevalence of use and does not imply particular suspicion of endocrine activity.[88]

Genetic damage[edit]

Several studies have not found mutagenic effects,[89] so glyphosate has not been listed in the U.S. EPA/IARC databases.[90] Various other studies suggest glyphosate may be mutagenic.[90]

Other animals[edit]

A review of the ecotoxicological data on Roundup shows at least 58 studies of the effects of Roundup itself on a range of organisms exist.[55] This review concluded, "for terrestrial uses of Roundup minimal acute and chronic risk was predicted for potentially exposed non-target organisms".

In reproductive toxicity studies performed in rats and rabbits, no adverse maternal or offspring effects were seen at doses below 175–293 mg/kg of body weight per day.[26]

The EPA,[25] the EC Health and Consumer Protection Directorate, and the UN World Health Organization have all concluded pure glyphosate is not carcinogenic. Opponents of glyphosate claim Roundup has been found to cause genetic damage, citing Peluso et al.[91] The authors concluded the damage was "not related to the active ingredient, but to another component of the herbicide mixture".

A 2003 study of various formulations of glyphosate found, "[the] risk assessments based on estimated and measured concentrations of glyphosate that would result from its use for the control of undesirable plants in wetlands and over-water situations showed that the risk to aquatic organisms is negligible or small at application rates less than 4 kg/ha and only slightly greater at application rates of 8 kg/ha.".[92] A 2013 meta-analysis also reviewed the available data related to potential impacts of glyphosate-based herbicides on amphibians. According to the authors, the use of glyphosate-based pesticides cannot be considered the major cause of amphibian decline, the bulk of which occurred prior to the widespread use of glyphosate or in pristine tropical areas with minimal glyphosate exposure. The authors recommended further study of species- and development-stage chronic toxicity, of environmental glyphosate levels, and ongoing analysis of data relevant to determining what if any role glyphosate might be playing in worldwide amphibian decline, and suggest including amphibians in standardized test batteries.[93]

Glyphosate formulations are much more toxic for amphibians and fish than glyphosate alone.[72] Glyphosate formulations may contain a number of so-called ‘inert’ ingredients or adjuvants, most of which are not publicly known as in many countries the law does not require that they be revealed.[94]

A study published in 2010 proposed commercial glyphosate can cause neural defects and craniofacial malformations in African clawed frogs (Xenopus laevis). The experiments used frog embryos that were incubated with 1:5000 dilutions of a commercial glyphosate solution. The frog embryos suffered diminution of body size, alterations of brain morphology, reduction of the eyes, alterations of the branchial arches and otic placodes, alterations of the neural plate, and other abnormalities of the nervous system. The authors suggested glyphosate itself was responsible for the observed results because injection of pure glyphosate produced similar results in a chicken model.[95]

Monsanto and other companies produce glyphosate products with alternative surfactants specifically formulated for aquatic use, for example the Monsanto products "Biactive" and "AquaMaster".[96][97] In 2001, the Monsanto product Vision® was studied in a forest wetlands site in Canada. Substantial mortality occurred only at concentrations exceeding the expected environmental concentrations as calculated by Canadian regulatory authorities. While it was found that site factors such as pH and suspended sediments substantially affected the toxicity in the amphibian larvae tested, overall, "results suggest that the silvicultural use of Vision herbicide in accordance with the product label and standard Canadian environmental regulations should have negligible adverse effects on sensitive larval life stages of native amphibians."[98]

Effect on plant health[edit]

A correlation was found between an increase in the infection rate of wheat by Fusarium head blight and the application of glyphosate, but "because of the nature of this study, we could not determine if the association between previous GF (glyphosate formulation) use and FHB development was a cause-effect relationship".[99] Other studies have found causal relationships between glyphosate and decreased disease resistance.[100]

Weed resistance[edit]

Resistance evolves after a weed population has been subjected to intense selection pressure in the form of repeated use of a single herbicide.[101][102] Weeds resistant to the herbicide have been called 'superweeds'.[103] The first documented cases of weed resistance to glyphosate were found in Australia in 1996, involving rigid ryegrass (Lolium rigidum) near Orange, New South Wales.[104][105] In 2006, farmers associations were reporting 103 biotypes of weeds within 63 weed species with herbicide resistance.[106] In 2009, Canada identified its first resistant weed, giant ragweed, and at that time 15 weed species had been confirmed as resistant to glyphosate.[101][107] As of 2010, in the United States 7 to 10 million acres (28,000 to 40,000 km2) of soil were afflicted by superweeds, or about 5% of the 170 million acres planted with corn, soybeans, and cotton, the crops most affected, in 22 states.[108] In 2012, Charles Benbrook reported that the Weed Science Society of America listed 22 super weeds in the U.S., with over 5.7 million has (14 million ac) infested by GR weeds and that Dow AgroSciences had carried out a survey and reported a figure of around 40 million ha (100 million ac).[109] As of 2014, the International Survey of Herbicide Resistant Weeds database listed 211 weeds that were resistant to glyphosate.[110]

In response to resistant weeds, farmers are hand-weeding, using tractors to turn over soil between crops, and using other herbicides in addition to glyphosate.

Palmer amaranth[edit]

Amaranthus palmeri

In 2004, a glyphosate-resistant variation of Amaranthus palmeri, commonly known as Palmer amaranth, was found in Georgia and confirmed by a 2005 study.[111] In 2005, resistance was also found in North Carolina.[112] Widespread use of Roundup Ready crops led to an unprecedented selection pressure, and glyphosate resistance followed.[112] The weed variation is now widespread in the southeastern United States.[113] Cases have also been reported in Texas[113] and Virginia.[114]


Conyza bonariensis (also known as hairy fleabane and buva) and Conyza canadensis (known as horseweed or marestail), are other weed species that had lately developed glyphosate resistance.[115][116][117] A 2008 study on the current situation of glyphosate resistance in South America concluded "resistance evolution followed intense glyphosate use" and the use of glyphosate-resistant soybean crops is a factor encouraging increases in glyphosate use.[118]


Ryegrass Lolium perenne

Glyphosate-resistant ryegrass (Lolium) has occurred in most of the Australian agricultural areas and other areas of the world. All cases of evolution of resistance to glyphosate in Australia were characterized by intensive use of the herbicide while no other effective weed control practices were used. Studies indicate the resistant ryegrass does not compete well against nonresistant plants and their numbers decrease when not grown under conditions of glyphosate application.[119]

Johnson grass[edit]

Glyphosate-resistant Johnson grass (Sorghum halepense) is found in glyphosate-resistant soybean cultivation in northern Argentina.[120]

Legal cases[edit]

Advertising controversy[edit]

The New York Times reported that in 1996, "Dennis C. Vacco, the Attorney General of New York, ordered the company to pull ads that said Roundup was "safer than table salt" and "practically nontoxic" to mammals, birds and fish. The company withdrew the spots, but also said that the phrase in question was permissible under E.P.A. guidelines."[121]

Scientific fraud[edit]

On two occasions, the United States EPA has caught scientists deliberately falsifying test results at research laboratories hired by Monsanto to study glyphosate.[122] The first incident involved Industrial Biotest Laboratories (IBT). The United States Justice Department closed the laboratory in 1978, and its leadership was found guilty in 1983 of charges of falsifying statements, falsifying scientific data submitted to the government, and mail fraud.[123] In 1991, Don Craven, the owner of Craven Laboratories and three employees were indicted on 20 felony counts. Craven, along with fourteen employees were found guilty of similar crimes.[124]

Monsanto has stated the Craven Labs investigation was started by the EPA after a pesticide industry task force discovered irregularities, that the studies have been repeated, and that Roundup's EPA certification does not now use any studies from Craven Labs or IBT.[122]

Trade dumping allegations[edit]

United States companies have cited trade issues with glyphosate being dumped into the western world market areas by Chinese companies and a formal dispute was filed in 2010.[125][126]

Genetically modified crops[edit]

Some micro-organisms have a version of 5-enolpyruvoyl-shikimate-3-phosphate synthetase (EPSPS) resistant to glyphosate inhibition. A version of the enzyme that both was resistant to glyphosate and that was still efficient enough to drive adequate plant growth was identified by Monsanto scientists after much trial and error in an Agrobacterium strain called CP4, which was found surviving in a waste-fed column at a glyphosate production facility.[127][128][129]:56 This CP4 EPSPS gene was cloned and transfected into soybeans. In 1996, genetically modified soybeans were made commercially available.[130] Current glyphosate-resistant crops include soy, maize (corn), canola, alfalfa, and cotton, with wheat still under development.

Genetically modified crops have become the norm in the United States. For example, in 2010, 70% of all the corn, 78% of cotton, and 93% of all soybeans planted were herbicide-resistant.[131]

See also[edit]

External links[edit]


  1. ^ a b Glyphosate, Environmental Health Criteria monograph No. 159, Geneva: World Health Organization, 1994, ISBN 92-4-157159-4 
  2. ^ Index no. 607-315-00-8 of Annex VI, Part 3, to Regulation (EC) No 1272/2008 of the European Parliament and of the Council of 16 December 2008 on classification, labelling and packaging of substances and mixtures, amending and repealing Directives 67/548/EEC and 1999/45/EC, and amending Regulation (EC) No 1907/2006. OJEU L353, 31.12.2008, pp 1–1355 at pp 570, 1100..
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