Concentrations Of Glyphosate Research Articles

Isolation and Characterization of Glyphosate Degrading Bacteria from Kubau Local Govt. Area, Kaduna State

Strains of bacteria with the ability of utilizing glyphosate as the sole source of carbon were isolated from soil exposed to glyphosate herbicide by culture enrichment method and identified through partial 16S rRNA gene sequence analysis. Sixteen different microbial strains were isolated from glyphosate-contaminated sites in Kubau local govt. area, Kaduna state. Two of the microbial strains: BBDD3 and BBD4 were found to be the best degraders and were able to withstand up to 16.4 mg/ml of the glyphosate concentration. On the basis of 16s rRNA and biochemical tests, BBDD3 and BBDD4 strains were identified as Escherichia coli and Sporanaerobacter acetigenes respectively. These strains demonstrate laboratory utilizing ability of 92% and 98% for 16.4 mg/ml of the glyphosate formulation, respectively. The best optimum conditions for degradation were observed at pH 6.0 for the strains and at the temperature of 35oC for strain BBDD3 and BBDD4. Based on these results, the two strains displayed their potentials to be used in the bioremediation of glyphosate-contaminated environment.

Isolation and optimization of a glyphosate-degrading Rhodococcus soli G41 for bioremediation.

A widely used herbicide for controlling weeds, glyphosate, is causing environmental pollution. It is necessary to remove it from environment using a cost-effective and eco-friendly method. The aims of this study were to isolate glyphosate-degrading bacteria and to optimize their degradative conditions required for bioremediation. Sixteen bacterial strains were isolated through enrichment and one strain, Rhodococcus soli G41, demonstrated a high removal rate of glyphosate than other strains. Response surface methodology was employed to optimize distinct environmental factors on glyphosate degradation of G41 strain. The optimal conditions for the maximum glyphosate degradation were found to have the NH4Cl concentration of 0.663% and glyphosate concentration of 0.115%, resulting in a maximum degradation of 42.7% after 7days. Bioremediation analysis showed 47.1% and 40% of glyphosate in unsterile soil and sterile soil was removed by G41 strain after 14days, respectively. The presence of soxB gene in G41 strain indicates that the glyphosate is degraded via the eco-friendly sarcosine pathway. The results indicated that G41 strain has the potential to serve as an in-situ candidate for bioremediation of glyphosate polluted environments.

Herbicide residues in Australian grain cropping soils at sowing and their relevance to crop growth

Herbicides are used extensively in Australian grain cropping systems. Despite occasional observations of herbicide-induced phytotoxicity, there is little information on the persistence and carryover of multiple herbicide classes in cropping soils and the risk to subsequent crops. Two soil surveys were conducted, in 2015 (n = 40) and 2016 (n = 42), across different Australian grain cropping fields prior to sowing of winter crops, and soil samples analysed for herbicide residues (16 analytes in 2015 and 22 analytes in 2016). Samples in 2015 were taken at two depths (0–10 cm and 10-30 cm), whilst samples in 2016 were taken in topsoil (0–10 cm) only, but from two discrete locations in each field. Our research in both years found at least one herbicide (or herbicide metabolite) residue at all sites, with a median of 6 analytes detected in 2015 and 7 analytes detected in 2016. The most frequently detected residues were glyphosate and its primary breakdown product aminomethylphosphonic acid (AMPA), in 87 and 100%, respectively, of topsoil (0–10 cm) samples in 2015, and 67 and 93% of samples in 2016. The median concentration of glyphosate in 2015 was 0.12 mg kg−1, while AMPA was 0.41 mg kg−1. In 2016, median concentrations of glyphosate and AMPA were 0.22 mg kg−1 and 0.31 mg kg−1. Residues of 2,4-dichlorophenoxyacetic acid, trifluralin and diflufenican were also detected in >40% of topsoil samples in both seasons, but with median concentrations of <0.05 mg kg−1. A literature review found limited availability of phytotoxicity thresholds for major grain crops exposed to soilborne herbicide residues. A risk assessment using available thresholds suggested that although up to 29% of fields contained trifluralin residues that could constrain cereal crop growth, and 24% of fields contained residues of phenoxy or sulfonylureas that could affect dicotyledonous crops, the majority of these fields when planted with tolerant crops would be unlikely to be affected by herbicide residues. More work is required to ascertain the spatial distribution, bioavailability and phytotoxicity of residues and residue mixtures to enable a more accurate agronomic risk assessment.

Developmental toxicity of glyphosate on embryo-larval zebrafish (Danio rerio)

Glyphosate (GLY) induces developmental toxicity in fish, but research on the toxicity mechanism is limited. In this study, zebrafish embryos were exposed for 120 hpf to 0.7, 7, and 35 mg L-1 GLY. The results show that GLY treatment induced developmental toxicity in the fish, including premature hatching, reduced heartbeats, pericardial and yolk sac oedema, swim bladder deficiency, and shortened body length, which was possibly due to a significantly decreased triiodothyronine (T3)/thyroxine (T4) ratio and the abnormal expression patterns of hypothalamic-pituitary-thyroid (HPT) (crh, tshβ, tr α, tr β, and t tr ) and growth hormone/insulin-like growth factor (GH/IGF) axis-related genes (gh, ghrα, ghrβ, igf1, igf1rα, and igf1rβ) in larvae exposed to GLY. In addition, GLY exposure altered the levels of SOD and CAT, increased ROS, promoted malondialdehyde (MDA) content, and significantly altered the levels of endoplasmic reticulum (ER) stress signalling pathway factors (perk, eif2α, gadd34, atf4, ire1α, xbp1, atf6, hspa5, and chop), suggesting that GLY treatment induced oxidative injury and ER stress in the larvae. Further research showed that treatment with a higher concentration of GLY upregulated the levels of iNOS, IL-1β, and TNF-α while inhibiting the expression of IL-10 and TGF-β, suggesting that GLY causes an inflammatory reaction in the larvae. In addition, we also found that apoptosis was induced in the larvae, which was determined by acridine orange staining and abnormal expression of p53, caspase-3, -8, and -9. Taken together, our results demonstrate that GLY exposure altered the T3/T4 ratio, disturbed the expression patterns of HPT and GH/IGF axis-related genes, and induced oxidative and ER stress, inflammatory reactions, and apoptosis in the zebrafish larvae. This investigation contributes to improved understanding of the developmental toxicity mechanism of GLY in fish.

Association of Glyphosate Exposure with Blood DNA Methylation in a Cross-Sectional Study of Postmenopausal Women.

Background:Glyphosate is the most commonly used herbicide in the world and is purported to have a variety of health effects, including endocrine disruption and an elevated risk of several types of cancer. Blood DNA methylation has been shown to be associated with many other environmental exposures, but to our knowledge, no studies to date have examined the association between blood DNA methylation and glyphosate exposure.Objective:We conducted an epigenome-wide association study to identify DNA methylation loci associated with urinary glyphosate and its metabolite aminomethylphosphonic acid (AMPA) levels. Secondary goals were to determine the association of epigenetic age acceleration with glyphosate and AMPA and develop blood DNA methylation indices to predict urinary glyphosate and AMPA levels.Methods:For 392 postmenopausal women, white blood cell DNA methylation was measured using the Illumina Infinium MethylationEPIC BeadChip array. Glyphosate and AMPA were measured in two urine samples per participant using liquid chromatography–tandem mass spectrometry. Methylation differences at the probe and regional level associated with glyphosate and AMPA levels were assessed using a resampling-based approach. Probes and regions that had an false discovery rate in of 1,000 subsamples of the study population were considered differentially methylated. Differentially methylated sites from the probe-specific analysis were combined into a methylation index. Epigenetic age acceleration from three epigenetic clocks and an epigenetic measure of pace of aging were examined for associations with glyphosate and AMPA.Results:We identified 24 CpG sites whose methylation level was associated with urinary glyphosate concentration and two associated with AMPA. Four regions, within the promoters of the MSH4, KCNA6, ABAT, and NDUFAF2/ERCC8 genes, were associated with glyphosate levels, along with an association between ESR1 promoter hypomethylation and AMPA. The methylation index accurately predicted glyphosate levels in an internal validation cohort. AMPA, but not glyphosate, was associated with greater epigenetic age acceleration.Discussion:Glyphosate and AMPA exposure were associated with DNA methylation differences that could promote the development of cancer and other diseases. Further studies are warranted to replicate our results, determine the functional impact of glyphosate- and AMPA-associated differential DNA methylation, and further explore whether DNA methylation could serve as a biomarker of glyphosate exposure. https://doi.org/10.1289/EHP10174

Glifosatın glukoz-6-fosfat dehidrogenaz enzim aktivitesi üzerindeki etkisinin in vitro koşullarda değerlendirilmesi

Purpose: The aim of this study was to investigate in vitro effect of glyphosate on Glucose 6-phosphate dehydrogenase (G6PD) enzyme activity.&#x0D; Materials and Methods: In terms of G6PD enzyme deficiency, samples taken from healthy and enzyme deficient male individuals were studied. After the hemolysates were prepared from blood sample, G6PD enyzme activities were determined by the modified Beutler method. Then, the effects of different concentrations (5.3x10-3, 5.3x10-4, 5.3x10-5, 5.3x10-6 mmol/mL) of glyphosate on G6PD activity were evaluated in normal and mutant enzymes. In addition, the in vitro effect of the antioxidant N-acetylcysteine (NAC) on the enzyme was investigated in the presence of glyphosate and without glyphosate.&#x0D; Results: While the result of normal erythrocyte G6PD activity was 12U/g for the individual, the result for the individual with enzyme deficiency was 2.5U/g Hb. The glyphosate’s maximum activity loss in the G6PD enzyme was observed in the 60th minute incubation. The highest inhibition was observed at 5.3x10-3 mmol/mL glyphosate. 4.7x10-7 mmol/mL N-Acetylcysteine partially increased the inhibition of glyphosate in the G6PD enzyme in healthy individuals, but had no effect on mutant G6PD.&#x0D; Conclusion: In humans, it is predicted that glyphosate affects G6PD enzyme activity in vitro and is an interference agent in the experimental process. In case of contamination, studies on limits of glyphosate that will not cause harmful effects in humans should be continued.

CONCENTRATIONS OF GLYPHOSATE IN SURFACE WATER, SEDIMENT AND FISH IN OSSIOMO RIVER, NIGERIA

Glyphosate concentrations were determined in water, sediment and fish (Brycinus macrolepidotus) samples from designated areas with intense agricultural activities along Ossiomo River, Nigeria. Three sampling stations were selected to reflect areas of possible sources of pollution. The pesticide analysis was carried out using Gas chromatography (GC) equipped with electron capture detector. Levels of glyphosate in water ranged from 0.004 – 0.006 mg/l, sediment, 0.008 – 0.015 mg/kg and fish, 0.010 – 0.034 mg/kg dw. The pesticide concentrations in fish were significantly (p&lt;0.05) higher than water and sediment.The sediment log BSAFs (0.1– 0.4) were lower than the water log BCFs (0.4–0.8), an indication of the high affinity of glyphosate to sediments and lipid tissues. However, the observed glyphosate concentrations in the matrices were lower than the maximum contaminant level (MCL).Estimated health risk assessment indicated that glyphosate concentrations in the fish (Brycinus macrolepidotus) from Ossiomo River do not pose cancer risk to humans on consumption.

Time to kill the beast – Importance of taxa, concentration and timing during application of glyphosate to knotweeds

AbstractKnotweeds (Fallopia spp., syn. Reynoutria spp.) are among the most invasive plants globally, mainly due to their ability to regenerate from rhizomes and their extremely high biomass production. Spraying with glyphosate is a common control method, yet little is known about its effectiveness on underground rhizomes. In addition, there are concerns about the negative environmental impact of glyphosate. Therefore, it is essential to use appropriate dosages and application times to avoid overuse. Based on a pot trial and field experiments, we assessed the effectiveness of glyphosate concentration, application time, and influence of glyphosate on rhizomes from different soil depths to determine their effect on the aboveground and belowground parts of knotweed plants of different taxa. The study demonstrates that sampling rhizomes is a more consistently accurate indicator of knotweed regeneration rate than sampling shoots. Regeneration of shoots and rhizomes was affected differently by glyphosate spraying depending on the application time. The effect on rhizomes was much greater with early season spraying than late season spraying, which primarily reduced shoot biomass. However, no differences were found between rhizome vitality at different soil depths. F. sachalinensis was sufficiently controlled by early season foliar spray with 5% glyphosate (3.65 kg a.i. ha−1) in contrast to F. japonica and F. ×bohemica. For rapid and targeted control, early season foliar spray with 8% glyphosate (5.85 kg a.i. ha−1) is needed and, in the case of the hybrid, for a minimum of two consecutive seasons.

Mild chronic exposure to pesticides alters physiological markers of honey bee health without perturbing the core gut microbiota

Recent studies highlighted that exposure to glyphosate can affect specific members of the core gut microbiota of honey bee workers. However, in this study, bees were exposed to relatively high glyphosate concentrations. Here, we chronically exposed newly emerged honey bees to imidacloprid, glyphosate and difenoconazole, individually and in a ternary mixture, at an environmental concentration of 0.1 µg/L. We studied the effects of these exposures on the establishment of the gut microbiota, the physiological status, the longevity, and food consumption of the host. The core bacterial species were not affected by the exposure to the three pesticides. Negative effects were observed but they were restricted to few transient non-core bacterial species. However, in the absence of the core microbiota, the pesticides induced physiological disruption by directly altering the detoxification system, the antioxidant defenses, and the metabolism of the host. Our study indicates that even mild exposure to pesticides can directly alter the physiological homeostasis of newly emerged honey bees and particularly if the individuals exhibit a dysbiosis (i.e. mostly lack the core microbiota). This highlights the importance of an early establishment of a healthy gut bacterial community to strengthen the natural defenses of the honey bee against xenobiotic stressors.

Derivation of water quality criteria for glyphosate and its formulations to protect aquatic life in China.

Extensive use of the herbicide glyphosate leads to a high detection rate in the environment and potential risks to nontarget aquatic life. China ranks first globally in the production and consumption of glyphosate, but there are no glyphosate water quality criteria (WQCs) for protecting aquatic life. Here, data on the acute and chronic toxicity of glyphosate and glyphosate-based formulations (GBFs) to freshwater aquatic life were collected and screened. Significant differences in species sensitivity distributions (SSDs) and toxicity values for acute or chronic toxicity were found between glyphosate and GBFs. The hazardous concentrations for 5% of species (HC5) of glyphosate or GBFs between native and nonnative species were different, and native species were found to be more sensitive to the toxicity of glyphosate. The acute and chronic WQCs derived with the SSD method for glyphosate based on the toxicity data for native species in China were 3.35 and 0.26mg/L, respectively, and those found for GBFs were 0.21 and 0.005mg/L, respectively. The WQCs in this study were quite different from those estimated using similar statistical extrapolation methods in other countries, which reflects the differences in species sensitivity to glyphosate toxicity in different regions. The hazard quotients (HQs) were calculated based on the WQCs and concentrations of glyphosate in some surface waters in China and indicated that glyphosate exhibits medium or high hazard risk in some samples of Tai Lake, surface water in Guiyang, fishpond water in Chongqing, rural drinking water, and surface water and reservoir water in Henan Province. The WQCs of glyphosate and GBFs have scientific significance for the exposure and pollution control of herbicide formulations and the protection of aquatic life in China.

Assessment of the bioaccessibility of glyphosate in soil using a physiologically based extraction test

The herbicide glyphosate (N-(phosphonomethyl) glycine) is among the most extensively used agrichemicals worldwide. The environmental fate of glyphosate has been well studied, revealing that glyphosate rapidly binds to soil. The objective of this study was to provide an initial assessment of whether this binding also reduces the bioaccessibility of glyphosate under simulated gastrointestinal tract conditions, and therefore might diminish bioavailability and risk from incidental ingestion of glyphosate contaminated soil in humans. Five soil samples were constructed to vary in composition with respect to aluminum, iron, phosphate, clay, and carbon content —factors that have been shown to influence glyphosate soil binding. Bioaccessibility of glyphosate at 4 or 40 mg/kg was evaluated in each soil sample using a Physiologically Based Extraction Test (PBET). Bioaccessibility of glyphosate at 4 mg/kg was significantly decreased by elevated aluminum and iron (p < 0.001) in the stomach phase, but not at the higher concentration or in the intestinal phase. Bioaccessibility of glyphosate was essentially complete in all other soils at both glyphosate concentrations. Although there are acknowledged limitations in the study, the results suggest that the relative oral bioavailability (RBA) of glyphosate from soil may be at or near 100% for human health risk assessment purposes.

Genotoxicity of Glyphosate on Cultured Human Lymphocytes.

Glyphosate-based herbicides are the most used herbicides in the world. Despite being widely used, a dispute exists whether glyphosate-based herbicides have a negative effect on human health, particularly genotoxic effects. Therefore, the aim of this study was to investigate glyphosate genotoxicity on cultured human lymphocytes. Cultured human lymphocytes were treated with different concentrations of glyphosate (20, 40, and 200µmol/L). Four toxicity measures were examined: frequency of chromosomal aberrations (CAs), frequency of sister-chromatid exchange (SCE), production of 8-OHdG, and cell kinetics analysis. The results show that glyphosate induced significant (P < 0.05) increases in the levels of SCE at the highest used concentration (200μmol/L). However, no significant elevation in SCE levels was observed at the lower examined concentrations (20 and 40μmol/L). No significant changes in CA were detected at all examined concentrations (P = 0.86). Also, glyphosate did not induce changes to the normal level of 8-OHdG at all examined concentrations (P = 0.98). Last, no significant changes in either mitotic index or proliferative index were observed at any examined concentrations (P > 0.05). The results collectively indicate a lack of genotoxicity and cytotoxicity of glyphosate in cultured human lymphocytes when dealing with environmentally relevant concentrations (20 and 40μmol/L). However, being exposed to higher concentrations (200μmol/L) led to slightly higher level of SCE. Therefore, we recommend cautionary measures when dealing with glyphosate-based herbicides for individuals, such as farmers, who may be extensively exposed to high concentrations of these herbicides.

Glyphosate and AMPA exposure in relation to markers of biological aging in an adult population-based study.

Glyphosate, a broad-spectrum herbicide, and its main metabolite aminomethylphosphonic acid (AMPA) are persistent in the environment. Studies showed associations between glyphosate or AMPA exposure and several adverse cellular processes, including metabolic alterations and oxidative stress. To determine the association between glyphosate and AMPA exposure and biomarkers of biological aging. We examined glyphosate and AMPA exposure, mtDNA content and leukocyte telomere length in 181 adults, included in the third cycle of the Flemish Environment and Health Study (FLEHSIII). DNA was isolated from leukocytes and the relative mtDNA content and telomere length were determined using qPCR. Urinary glyphosate and AMPA concentrations were measured by Gas Chromatography-Tandem Mass Spectrometry (GC-MS-MS). We used multiple linear regression models to associate mtDNA content and leukocyte telomere length with glyphosate or AMPA exposure while adjusting for confounding variables. A doubling in urinary AMPA concentration was associated with 5.19% (95% CI: 0.49 to 10.11; p=0.03) longer leukocyte telomere length, while no association was observed with urinary glyphosate concentration. No association between mtDNA content and urinary glyphosate nor AMPA levels was observed. This study showed that AMPA exposure may be associated with telomere biology in adults.

High Rates of Biochar Soil Amendment Cause Increased Incidences of Neurotoxic and Oxidative Stress in Eisenia fetida (Oligochaeta) Exposed to Glyphosate

Despite several known beneficial attributes, biochar is suspected to cause harm to soil organisms when present in relatively high quantities in the soil. To determine the potential detrimental effects of biochar, for 96 h, we exposed the earthworm Eisenia fetida to 0, 2, 4 and 8 mg glyphosate (GLY) per kg in non-amended and biochar-amended soil at rates of 5, 10 and 15%. The results indicated that in non-amended soil, survival was significantly decreased in the highest GLY concentration. Although no median lethal concentration (LC50) could be computed due to the lack of sufficient mortality, in the absence of biochar, a lethal concentration 10% (LC10) of 5.540 mg/kg and a lethal concentration 20% (LC20) of 7.067 mg/kg were calculated. In the biochar-amended soil, no mortality occurred in the control and GLY treatments for all three biochar amendment rates. Biomass results showed significant biomass loss in the highest GLY treatment in the absence of biochar, with an effective concentration of 10% (EC10) of 5.23 mg/kg and an effective concentration of 20% (EC20) of 6.848 mg/kg. In the amended soil, overall, slight non-significant increases in biomass were recorded and no effective concentrations could be calculated due to the lack of significant biomass loss. The assessment of neurotoxicity via the activity of acetylcholine esterase (AChE) showed no change in AchE due to GLY in all the non-amended treatments. However, in the biochar-amended treatments, statistically high levels of AchE occurred (p &lt; 0.05) even in the control (in the absence of GLY). The assessment of oxidative stress through catalase (CAT) activity, showed similar results with no significant effects of GLY alone on CAT activity, but rather dramatic increases in activity in the control and GLY treatments in the biochar-amended soil, with one significant increase in the 10% amended in 8 mg GLY/Kg (p &lt; 0.05). Such significant increases in both AChE and CAT were only observed in soil amended with 10 and 15% biochar. Our findings show that although seemingly beneficial for whole body endpoints, biomarker responses indicate that a biochar amendment higher than 5% adds considerable additional stress to earthworms and should be avoided.

Determination of Glyphosate and AMPA in Blood Can Predict the Severity of Acute Glyphosate Herbicide Poisoning.

To evaluate a potential association between blood and urine concentration of glyphosate and its metabolite, aminomethylphosphonic acid (AMPA), with severity of acute glyphosate (herbicide) poisoning. In our retrospective study of acute glyphosate poisoning, we examined records from the French National Database of Poisonings, dated between January 1, 2004, and December 31, 2016. We compared the severity of poisoning among case individuals using the Fisher exact test and Wilcoxon test. Also, we calculated ROC curves to determine the cutoff for blood and urine concentration. A total of 17 plasma glyphosate, 11 urine glyphosate, 13 plasma AMPA, and 10 urine AMPA specimens were included in our study, with collection dates ranging from January 1, 2004, through December 31, 2016. The optimal cutoff we discovered for blood concentration of AMPA was 0.88 mg/L; for glyphosate, it was 600 mg/L. The cutoff plasma concentration of AMPA has never been described in the literature, to our knowledge.

Development of an LC-MS/MS Method for Non-Invasive Biomonitoring of Neonicotinoid and Systemic Herbicide Pesticide Residues in Bat Hair.

With over a quarter of the world’s bats species facing extinction, there is a need for ecotoxicological studies to assess if acute and sublethal exposure to newer pesticides such as neonicotinoids and carbonates contribute to population declines. Pesticide exposure studies in bats have been limited to terminal sampling methods, therefore we developed a non-invasive liquid chromatography-tandem mass spectrometry (LC-MS/MS) method utilizing hair trimmings. The hair of big brown bats (Eptesicus fuscus) was collected and pooled by county to assess the best extraction solvent and solid-phase-extraction (SPE) clean-up cartridges. Using the best performing extraction solvent, methanol, and the best performing SPE cartridge, Chromabond HR-X, we developed an optimized multiple reaction monitoring (MRM) LC-MS/MS method for simultaneous determination of 3 neonicotinoids, clothianidin, imidacloprid, and thiamethoxam; 1 carbonate, carbaryl; and 4 systemic herbicides, 2,4-D, atrazine, dicamba, and glyphosate. The optimized protocol yielded the detection of 3–8 of the compounds in the county-level bat hair pools. 2,4-D, glyphosate, and imidacloprid were found in all samples with two of the county-level hair samples having glyphosate concentrations of over 3500 pg/mg of hair. This approach has great potential to facilitate non-terminal ecotoxicological studies assessing the effects of subacute (chronic) pesticide exposure in threatened and endangered bat species and other species experiencing population declines.

Determination of glyphosate exposure in the Iberian hare: A potential focal species associated to agrosystems

Glyphosate is the most used herbicide worldwide. It is a small and highly polar pesticide whose physicochemical properties makes its analytical determination difficult. Here, a procedure based on liquid chromatography-high resolution tandem mass spectrometry (LC-HRMS/MS) was developed for glyphosate determination in samples of gastric content from wildlife. Iberian hare (Lepus granatensis), a herbivorous mammal species, strongly associated to agrosystems was selected as model species. The procedure involves direct analysis of sample without derivatization or instead of neither further cleaning steps. The procedure was validated by inter-day accuracy and precision studies with gastric content of hare spiked with glyphosate at ecologically relevant concentrations for the species (0.1–6 μg/g), and with 1 μg/g of isotopically labelled internal standard (glyphosate-2-13C,15N). Finally, glyphosate residues in hunted animals from pesticide-treated and pesticide-free areas (n = 75 and 28, respectively), as well as from hares found dead in the field (n = 11) were analysed. The linearity of both standards in extraction solutions and procedural calibration curves with spiked samples was similar, both with determination coefficients (r2) higher than 0.99. Satisfactory recoveries in spiked samples were achieved within the range of 95% to 118% (CV ≤ 20%). The limit of detection of glyphosate in hare gastric content was 0.03 μg/g. Prevalence of glyphosate in hunted animals from pesticide-treated areas ranged between 9 and 22%, increasing to 45% in animals found dead. The glyphosate concentrations detected in the gastric content of hares ranged from 0.11 to 16 μg/g. No residues were detected in animals from pesticide-free areas. In practice, the developed methodology may be particularly useful in the context of research and other work on the exposure in wildlife of one of the most used pesticides nowadays.

The Effect of Co-Exposure to Glyphosate, Cadmium, and Arsenic on Chronic Kidney Disease

The usage of glyphosate is increasing worldwide. Glyphosate and its major metabolite, aminomethylphosphonic acid (AMPA), are of potential toxicological concern in unknown chronic kidney disease (CKDu). As with Cd and other elements, glyphosate exposure has been reported as risk factor for CKDu in farmers. This study aimed to evaluate the influence of co-exposure to glyphosate and metals or metalloids in chronic kidney disease (CKD). In this study, the urine samples from 55 patients with CKD and 100 participants without CKD were analyzed for glyphosate, arsenic (As), cadmium (Cd), and lead (Pb) concentrations, and estimated glomerular filtration rate (eGFR). Negative associations between glyphosate, AMPA, As, and Cd concentrations in the urine and eGFR were found for study subjects (p < 0.05). With regard to the effect of co-exposure, the odds ratios (OR) for subjects with an eGFR of < 60 mL/min/1.73 m2 was significant because of the high Cd concentration (> 1 μg/g creatinine; OR = 7.57, 95% CI = 1.91–29.95). With regard to the effect of co-exposure, the OR for subjects with an of eGFR < 45 mL/min/1.73 m2 was significant at high glyphosate concentration (> 1 μg/g creatinine; OR = 1.57, 95% CI = 1.13–2.16) and As concentration (> 1 μg/g creatinine; OR = 1.01, 95% CI = 1.00–1.02). These results showed that glyphosate, AMPA, As, and Cd have an effect on CKD; notably, Cd, As, and glyphosate exposure can be important risk factors after stage 3a of CKD, and that there was a co-exposure effect of As and glyphosate in CKD after stage 3b. The potential health impacts of glyphosate should be considered, especial for patients with CKD and eGFR below 45 mL/min/1.73 m2.

Mathematical Modelling of Glyphosate Molecularly Imprinted Polymer-Based Microsensor with Multiple Phenomena.

The massive and careless use of glyphosate (GLY) in agricultural production raises many questions regarding environmental pollution and health risks, it is then important to develop simple methods to detect it. Electrochemical impedance spectroscopy (EIS) is an effective analytical tool for characterizing properties at the electrode/electrolyte interface. It is useful as an analytical procedure, but it can also help in the interpretation of the involved fundamental electrochemical and electronic processes. In this study, the impedance data obtained experimentally for a microsensor based on molecularly imprinted chitosan graft on 4-aminophenylacetic acid for the detection of glyphosate was analyzed using an exact mathematical model based on physical theories. The procedure for modeling experimental responses is well explained. The analysis of the observed impedance response leads to estimations of the microscopic parameters linked to the faradic and capacitive current. The interaction of glyphosate molecules with the imprinted sites of the CS-MIPs film is observed in the high frequency range. The relative variation of the charge transfer resistance is proportional to the log of the concentration of glyphosate. The capacitance decreases as the concentration of glyphosate increases, which is explained by the discharging of the charged imprinted sites when the glyphosate molecule interacts with the imprinted sites through electrostatic interactions. The phenomenon of adsorption of the ions in the CMA film is observed in the low frequency range, this phenomenon being balanced by the electrostatic interaction of glyphosate with the imprinted sites in the CS-MIPs film.

Effect of a glyphosate formulation on freshwater plankton: A community combined metric approach

Aim: The aim of this study was to experimentally assess the effects of glyphosate formulation on plankton composition by using different community parameters through a mesocosm experiment. Methodology: A 600 l mesocosm experiment was performed for 7 days, including a control (without glyphosate) and two concentrations of glyphosate. Results: Glyphosate caused a significant decrease in cladoceran density and a significant increase in rotifer, Chlorophyceae, and Euglenophyceae densities. In addition, zooplankton size diversity as well as microalgal evenness diminished. Interpretation: The decrease in cladoceran density may have benefited rotifers since they are less competitive for food resources. Moreover, the decrease in cladoceran foraging pressure over Chlorophyceae and Euglenophyceae may have benefited them. The different tolerances and competitiveness within the plankton components make the structure of this community a good indicator of environmental disturbance.