Abstract
Glyphosate (GLY), the most widely used herbicide active ingredient (AI) in the world, is frequently detected in aquatic environments where it can affect non-target organisms. Globally, more than 2000 commercial GLY-based herbicides (GBHs) are used to control weeds. Non-target organisms are exposed to complex pesticide formulations under real environmental conditions, but the co-formulants contained in GBHs are classified as so-called inert and inactive ingredients in terms of their biological effects. The main objective of this comprehensive review is to compile the results of aquatic ecotoxicological studies on the side-effects of GLY, GBHs, and their formulating agents. Based on the results demonstrated for a variety of plant and animal aquatic organisms, oxidative stress appears to be a major trigger for these adverse effects, affecting the integrity of DNA and other biochemical functions. Furthermore, there is evidence of impairment of various physiological and behavioral functions. Adverse effects of GLY and GBHs have been observed even at very low concentrations. There are also differences in the sensitivity of the aquatic organisms tested, even with similar lifestyles, habitats or identical taxa. The studies typically investigate the short-term effects of a single exposure to GLY/GBH on a single species, whilst in reality multiple applications of GBHs together with other pesticides are common during a cropping cycle. Moreover, the interactions between GLY/GBHs and other aquatic contaminants are rarely studied. Higher toxicity of GBHs compared to GLY alone has often been observed, demonstrating that co-formulants can be highly toxic on their own and markedly increase the toxicity of the GBH formulation. The possible impurities in GBHs, such as heavy metals, can cause additional problems for the environment and food safety. The widespread and massive use of GBHs leads to increased exposure and environmental hazards. In addition, the need for a revision of the risk assessment system is emphasized. According to the results of aquatic ecotoxicological studies, the current use and pollution of the aquatic environment by GLY/GBHs is highly problematic and cannot be considered environmentally sustainable. It is, therefore, necessary to at least tighten the permitted forms of use.
Similar content being viewed by others
Introduction
Over the last decade, an increasing number of scientific studies have investigated the effects of the most widely used herbicide active ingredient (AI) glyphosate (GLY) on non-target organisms [1,2,3]. GLY (N-(phosphonomethyl)-glycine) is a phosphonomethyl derivative of the natural amino acid glycine [4]. Cultivation of GLY-tolerant (GT) genetically modified (GM) crops such as soybeans and maize in North and South America has led to a massive increase in the use of GLY-based herbicides (GBHs) and they have become the most widely used herbicide formulations in the last decade [5,6,7,8], despite their known water-polluting properties and the emergence of GLY-resistant weeds [1]. Based on a European survey, GBH sales were estimated at 44,250 tonnes of AI, while the average GLY use in 2017 was about 0.24 kg AI ha−1 [9]. The global market of GBHs was estimated at 4438.5 million USD in 2020 [10], but it is very difficult to find accurate and up-to-date data on global use and sales of GBHs because detailed sales data are withheld as commercially sensitive information [11].
GLY exerts its herbicidal activity by inhibiting 5-enoylpyruvylshikimate-3-phosphate synthase (EPSPS) of the shikimate metabolic pathway. This leads to a blockage of the biosynthesis of essential aromatic amino acids and consequently to plant death. The shikimate metabolic pathway is present in all plants and thus GLY acts as a non-selective broad-spectrum herbicide. However, the shikimate pathway is also present in most fungi and some bacteria, but it is absent in animals [12]. Therefore, the application of GBHs as non-selective herbicides not only causes the death of plant species, but can also negatively impact fungal and bacterial populations [13, 14]. In GBHs, different salts of GLY such as GLY-isopropylammonium salt (GLY-IPA), GLY-trimethylsulfonium salt or GLY-diammonium salts are used to enhance the solubility of the AI [15, 16]. In addition to GLY salts, various co-formulants are included in commercial GBH formulations. The key property of co-formulants is to act as surfactants enabling effective wetting and penetration of the plant cell wall, thereby permitting the AI to exert its herbicidal action [17]. For example, the use of POEA (a mixture of polyethoxylated tallow amines sold under product names such as MON 0818) in GBHs promotes GLY penetration into the plant cell [18]. Crucially from an environmental impact perspective, in addition to their designed herbicidal activity, GBHs have also been found to exert direct insecticidal effects on numerous non-target arthropod species including lacewings (Chrysoperla carnea) [19], spiders (e.g., Pardosa spp.) [20,21,22], mosquitos (Aedes aegypti larvae) [23], and pollinators such as bees (e.g., Megachile spp. and Apis mellifera) [24,25,26]. Whether these insecticidal effects of GBHs are due to GLY, the co-formulants, or a combination of the two cannot yet be accurately determined because most studies have not conducted a comparison between GLY and GBHs.
Co-formulants in commercial pesticides are considered to be inactive components in terms of the primary biological action of the formulation. As a result, co-formulants are usually listed as “inert” and their identity withheld on the packaging. Therefore, a simpler environmental risk assessment (ERA) has been deemed sufficient for co-formulants compared to AIs for regulatory purposes [27, 28]. Furthermore, regulatory authorities acquire data about co-formulants through individual stand-alone studies rather than considering them within formulations. Consequently, the differential effects of commercial pesticide formulations on ecosystems and humans are typically not due to the inherent attributes of co-formulants as independent components, but to how these co-formulants modify the toxicity of AIs [29]. However, numerous studies spanning many years have demonstrated the high toxicity of co-formulants and also the increased combined toxicity of AIs and co-formulants in various commercial pesticide formulations of all types (herbicides, insecticides, fungicides) compared to the toxicity of individual AIs. This applies to POEA, which is used as a co-formulant in GBHs [30,31,32], as well as its alternatives [33, 34]. Due to incriminating scientific evidence, the use of POEA in GBHs has been banned in the European Union (EU) by Regulation 2016/1313 [35].
Regulation of commercial pesticide formulations in the EU is based on a detailed and harmonized two-tier system [36]. AIs are registered at the EU community and managed by the European Commission, whilst commercial pesticide formulations are approved at the Member State level [37]. Several studies indicate that pesticide authorization needs to be revised [19, 38], including the re-evaluation of current testing systems during the registration process [19]. The approval and ERA for commercial pesticide formulations consider certain hazards but do not act through central regulation and restrictions. Moreover, EU Member States governments or their affiliated governmental organizations are required to take into account the positions of all stakeholders, including industry and also patent holders, during the risk assessment procedure [39].
Originally, non-selective GBHs were used exclusively for pre-emergence weed control. However, with the launch of GLY-tolerant genetically modified (GT GM) crops in 1996 (which are not authorized for cultivation in the EU) and the practice of pre-harvest desiccation in agriculture, the use of post-emergence GBHs has risen exponentially, leading to a vast increase in use over the last 25 years [6, 40, 41]. As a consequence of its escalating and excessive global use, GLY has become a ubiquitous pollutant in aquatic ecosystems [42]. Generally, GLY is directly sprayed onto crop fields not only for weed control but also for no-tillage farming, where a significant proportion is taken up by plants or enters the soil. In soil, GLY may be transported by surface water runoff, adsorbed to soil particles, enter groundwater by infiltration, or enter surface waters. The occurrence and concentration of GLY in the aquatic environment after its application are highly dependent on abiotic (e.g., pH, suspended materials, hydrological conditions), biotic (e.g., microbial composition), and climatic conditions (e.g., rainfall frequency and intensity) [43,44,45], in addition to the timing and frequency of pesticide treatments [44, 46]. In addition, GBH co-formulants such as POEA, similar to GLY, have been found to be widely distributed in the Midwest of the USA (e.g., Iowa, Illinois, Missouri) [47], where agricultural areas are large and the cultivation of genetically modified GT crops is concentrated [48]. Furthermore, POEA has been shown to persist in soil along with GLY and its primary metabolite aminomethylphosphonic acid (AMPA) [47, 49, 50], and can enter natural waterways [49, 51, 52]. Thus, GLY and co-formulants coexist in soil and water courses, although their combined toxic effects on the environment poorly are poorly understood.
Various aquatic organisms are directly or indirectly exposed to the harmful effects of GBH residues. To determine the potentially harmful effects of chemical contaminants on non-target aquatic organisms, a specific group of organisms is usually used in ecotoxicological studies to ensure environmental relevance. Examples of these test organisms include aquatic unicellular plant organisms (e.g., algae), aquatic invertebrates (e.g., water fleas) and vertebrates (e.g., fish). As part of the EU authorization process for pesticide formulation, an AI, safener or synergist shall only be approved, if the results of the risk assessment confirm acceptable or no risks [36]. As part of the tiered risk assessment for pesticides, the ecotoxicological test methods for assessing aquatic ecotoxicity are covered and summarized in the corresponding technical guidance document of the European Food Safety Authority (EFSA) [53]. The authorities of the EU Member States are responsible for ensuring the safety of pesticide formulations on the basis on the requirements of Regulation (EC) 1107/2009 [36].
Currently, the occurrence of GLY in surface waters is a global phenomenon, especially in regions where pre-harvest desiccation practices are widespread and the cultivation of GT GM crops takes place, so that the exclusive use of GBHs is extremely high. As a result, GLY contamination levels in surface water can reach up to 5200 µg l−1 [39, 54, 55]. The increased use GLY through desiccation or post-emergence application to GT GM crops generally increases the release of GLY and its co-formulants into the environment, which in turn leads to increased exposure. Such exposure can occur in any aquatic system, so increased toxicity can be exerted on all aquatic organism concerned, from aquatic microorganisms, algae and plants to aquatic invertebrates and vertebrates. Due to its amphoteric properties, GLY has both acidic and basic properties and is therefore highly soluble in water, although its detection in various environmental samples and matrices is difficult [56, 57]. In the past, GLY was not part of general pesticide monitoring programs, so environmental concentrations of GLY and its metabolites were underestimated. However, with advances in detection methods, GLY has been shown to be a ubiquitous environmental pollutant [58]. The primary metabolite of GLY, AMPA, is more mobile than the parent compound [59] and is also frequently detected in various environmental matrices such as groundwater, surface waters, soil, and air [39, 60,61,62,63]. However, it should be kept in mind that the presence of AMPA in environmental matrices such as groundwater, influents, or sewage sludge is not exclusive due to GLY metabolism, as it can also originate from phosphonate detergents used in various detergents [64].
Surveys of GLY residue levels in various water samples have shown a wide range of variation [39]. According to the U.S. Geological Survey, GLY and/or AMPA were detected in 59% of the 470 surface water sites analyzed, while the occurrence of the measured compounds in groundwater samples was less frequent (8.4% of 820 sample sites). AMPA was generally detected more often than GLY in the samples analyzed [51]. In surface waters collected in the Rio de Janeiro region, the GLY level detected was 2.6–10.1 µg l−1 (in > 40% of the samples analyzed) [65]. In Argentina, the average concentration of GLY and AMPA detected in surface water samples was in the range of 17.5–35.2 µg l−1 and 0.6–2.1 µg l−1, respectively [66]. However, maximum GLY and AMPA concentrations of up to 258 µg l−1 and 5865 µg l−1, respectively, were detected in the groundwater and surface water samples [52].
Based on the European monitoring studies over the past decade, the extent of GLY contamination in surface waters in the EU appears to be lower (typical GLY concentrations detected were between 0.05 and 0.85 μg l−1), although residues are consistently present [39]. In a monitoring study of sub-catchments with different land use (agricultural, urban) in Switzerland, the maximum GLY concentration of 4.15 μg l−1 was detected in the sampled water at peak discharge during storm events throughout the year, so that the seasonal concentration and occurrence of GLY cannot be explained by agricultural use alone [67]. According to a Dutch database with information on 161 sampling points, 90% of the surface water samples analyzed in 2020 contained GLY, while in 2019 only one sample contained GLY above 77 μg l−1 (152 sampling points) [68]. In Hungarian, Swiss, and Italian water samples, the GLY concentrations detected were between 0.035 ng ml−1 and 96 μg l−1 [39, 55, 69, 70]. However, GLY and AMPA concentrations in wastewater after rainfall can reach up to 384.9 μg l−1 and 47 μg l−1 [71]. The observed differences can primarily be explained by different agricultural locations, characteristics of the catchment area and natural precipitation conditions, which lead to different runoff and leaching of AI into surface waters [55]. Furthermore, co-formulants are also found in environmental compartments, although they are generally not monitored [48, 49], which may have adverse effects on non-target organisms [72, 73]. In summary, numerous scientific publications have demonstrated the highly unpredictable risks of GLY to aquatic ecosystems [39, 74, 75].
The objective of this review is to present and summarize pertinent information reported since the EU Commission Directive 2010/77/EU on the ecotoxicological adverse effects of GLY, GBHs, and their formulating agents on various non-target organisms and communities. This study not only presents the aquatic ecotoxicological concerns related to GLY/GBHs, but also summarizes the combined effects of GLY and GBHs with other aquatic pollutants (e.g., other pesticide residues, heavy metals, nano- and plastic particles) or pathogens. Systematic searches were conducted in scientific databases including Science Direct, Scopus, Web of Science, and other relevant databases. In addition, the references cited in the selected studies were also taken into account when necessary. Furthermore, non-public ecotoxicological studies financed and commissioned by the industry, that were not included in the application dossiers for re-approval [76] were excluded from evaluation. In total, an extensive reference database of more than 500 scientific publications dealing with the ecotoxicological aspects of GLY or GBHs was assessed. This review focuses specifically on the articles relating to aquatic ecosystems.
Ecotoxicity to aquatic organisms and ecosystems
Aquatic organisms are highly exposed to pollution as contact with waterborne xenobiotics is unavoidable. The ecotoxicity of GLY and GBHs has been studied in numerous aquatic organisms, including various algae species [77, 78], small planktonic crustacean such as Daphnia magna [79], molluscs [80], fish [81], and amphibians [82] (Fig. 1). Due to the long-lasting toxic effects of GLY, it is classified by the European Chemicals Agency ECHA as toxic to aquatic life (aquatic chronic 2; H411) [83]. However, a number of studies indicate that even at low concentrations GLY exhibits a toxicity to the aquatic environment that would justify a category 1 classification for chronic and even acute aquatic toxicity [81, 84]. In turn, GBHs are very rarely approved for use in the aquatic environment, yet GLY, its metabolite AMPA and co-formulants of GBHs are frequently detected in surface waters worldwide [85]. Moreover, as mentioned above, increased pollution levels by GLY residues due to the increased application of GLY during desiccation or on GT GM crops can affect all aquatic organism in the affected water bodies. This is a clear example of an increased likelihood of an existing hazard occurring due to the increased exposures to the aquatic pollutant.
Main ecotoxicological effects of glyphosate and its commercial formulations. Figure created with BioRender. Upward red arrows: increase; downward arrows: decrease; horizontal bi-directional arrows: alteration
Effects on aquatic microorganisms
Based on the scientific literature, the changes in aquatic microbial communities can be determined using direct (e.g., cell number, density, composition) and indirect (e.g., extracellular secretion, rate of leaf-litter breakdown, respiration) endpoints following GLY exposure [86,87,88,89,90]. As little as 10–100 μg l−1 GLY can cause direct adverse effects on most bacterioplankton taxa [91] and changes in the structure of freshwater microbial communities [87]. However, the effects on aquatic bacterial communities were usually observed at higher concentrations (≥ 2.5 mg l−1), resulting in a loss of biodiversity [88] (Table 1). In addition, a reduced decomposition rate of leaf-litter was observed in natural streams, possibly due to the negative effects of GLY (710 μg l−1) on the microbial community [90]. In artificial microcosms, GLY had no significant impact on the composition of the microbial community in water [92, 93], but community patterns of transcription were significantly altered [92]. The observed effects could be mainly due to the utilization of GLY by microorganisms as a phosphate source [92]. Furthermore, selective growth of different bacterial groups has also been demonstrated [94].
In aquatic environments, biofilms colonizing various artificial and natural substrates are compact communities of photoautotrophic (algae species) and heterotrophic microorganisms (bacteria, fungi, protozoa) embedded in their extracellular polymeric substance (EPS) secretions [89]. This EPS matrix is mainly composed of polysaccharides, proteins, lipids, nucleic acids and lectins, which can serve as sorption sites [95]. Scanning electron microscopy has revealed the intensive EPS production, primarily through secretion by heterotrophic microorganisms in freshwater biofilm communities after exposure to 100 µg l−1 GLY, particularly in the presence of the GBH co-formulant POEA [87]. This indicates a protective mechanism of bacterial and algal species in natural biofilms to remove and reduce the harmful effects of contaminants. Furthermore, GLY can affect the metabolic processes of bacteria and algae in biofilm communities [96]. The effects of GBH even at very low concentrations of 10 µg l−1 on the composition of the microbial community were significantly dependent on temperature. However, the effects of multiple stress factors on the microbial composition in water and sediment were completely opposite [97]. GLY at a high concentration of 2.54 g l−1 caused a significant reduction (− 47%) in the respiration of heterotrophic species in biofilm communities [86]. One type of Roundup GBH reduced the cell density of planktonic Pseudomonas aeruginosa under aerobic conditions, whereas planktonic anaerobic growth was increased in the presence of GLY (from 84.5 mg l−1) [98]. Furthermore, a concentration-dependent low growth of P. aeruginosa biofilms was also observed [98].
Based on a study conducted on the luminescent marine bacteria Vibrio fischeri and other test organisms such as crustaceans and plants, it was found that quaternary ammonium salts (e.g., diisopropylammonium chloroacetate) could be a safer alternative to GLY as they have lower toxicity but show comparable or slightly greater herbicidal activity compared to GLY [99]. However, the potential toxic effects of these quaternary ammonium salts on other non-target organisms remain to be investigated. Compared to Daphnia magna, V. fischeri was found to be nine times more sensitive to the toxic effects of Roundup formulations [100]. Moreover, aquatic test organisms were more sensitive to GBHs than soil microbial strains although a direct correlation between the toxicity of the formulations and the presence of POEA could not be demonstrated [100]. GLY and AMPA showed less negative effects in experiments with Tetrahymena pyriformi compared to V. fischeri, but with GLY displaying higher toxicity than AMPA in all cases [101]. However, no effects of Roundup on the aggregation behavior and cell morphology of Tetrahymena thermophila were observed, proteomic changes were indicated after GBH exposure (77.5–171 mg l−1) [102]. Monitoring of free-living pelagic and benthic biofilm-associated bacterial communities in microcosms revealed a transient increase in total cell number and bacterial diversity of pelagic bacterial communities in the water column due to the presence of GLY, while biofilm communities were less affected [103]. Various co-formulants can also be used as nutrient sources by bacterial communities in freshwater biofilms, especially under nutrient-poor conditions. For example, non-ionic tallow-based alkylbis(2-hydroxyethyl)amines can be utilized as carbon and energy sources by various Pseudomonas species during their growth [104].
Effects on algae species
The identification of potential harmful effects on non-target plant organisms is an essential part of the ecotoxicological evaluation of herbicides. Based on the available ecotoxicological studies, the various adverse effects of GLY have been detected at much lower concentrations (1–100 µg l−1) on phytoplankton communities compared to detectable GLY concentrations in surface waters. In many cases, however, the effects are only seen at much higher test concentrations (Table 2). A 48-h exposure to a Roundup GBH resulted in a significant reduction in growth and an increase in cell size of the unicellular green algae Selenastrum capricornutum with a 96-h EC50 value of 15.60 mg l−1 [78]. The most notable toxic effects were observed on the ultrastructure of exposed cells, including disruption of thylakoids and mitochondria, lipid accumulation, increased size and number of starch granules, and formation of electrodense bodies [78]. Larger cells of Scenedesmus vacuolatus, increased size of vacuoles and changed the stacking pattern of thylakoids after a 96-h exposure to the GBH Glifosato Atanor (containing 48% GLY as isopropylamine salt) at the range of 6–8 mg l−1 with an addition of 2.5% of the surfactant alkyl aryl polyglycol ether [105].
Moreover, altered oxidative stress parameters were also demonstrated. The observed effects can be attributed to an oxidative stress response resulting from the toxic mechanisms of the GBHs studied [105]. Furthermore, exposure to GBH Factor 540R affected the structure and functional properties of the freshwater phytoplankton community collected from agricultural areas in a concentration-dependent manner [106]. As a result, lower diversity (≥ 5 µg l−1) and pigment content (chlorophyll-a (chl-a) and carotenoids, ≥ 1 µg l−1) and altered biochemical and physiological parameters such as lipid peroxidation, antioxidant activity of catalase, superoxide dismutase (SOD), ascorbate peroxidase (≥ 500 µg l−1) [106], in addition to photosynthetic parameters (≥ 10 µg l−1) [107] were observed. It is worth noting that different algal and cyanobacterial species exhibit different sensitivity to GLY, even within the same taxa, resulting in significant differences in reported toxicity levels [108,109,110]. For instance, Pseudokirchneriella subcapitata showed a 72-h EC50 range of 24.7–41 mg l−1 [30, 111], while Desmodesmus subspicatus showed a 72-h EC50 range of 72.9–166 mg l−1 [112,113,114]. Exposure to a GBH (Roundup PowerFlex—4 mg a.e. GLY l−1) reduced algal community diversity by 6%, and the decreasing effect was much more pronounced at the higher test temperature (20 °C vs. 15 °C) [115]. However, the density of algae was not affected by the treatments. In addition, an interaction between herbicide and temperature was observed, indicating a temperature-specific effect of GBH on the diversity of algal community [115]. The growth of Chlorella vulgaris was promoted after individual and combined exposure to GLY and AMPA (≤ 0.5 mg l−1). In contrast, inhibition of algal growth was observed at the higher concentration tested (≥ 5 mg l−1) [116]. However, the inhibitory effect of AMPA was only demonstrated in the presence of GLY [116].
GBHs can act as chemical stressors on phytoplankton community structure and also stimulate the synthesis of cyanotoxins by cyanobacteria. Individual exposure to GBH Faena (1.02–2.70 mg l−1) resulted in reduced growth rates of the microalgae studied (Ankistrodesmus falcatus, C. vulgaris, P. subcapitata, and Scenedesmus incrassatulus), but stimulated the proliferation of the toxigenic cyanobacteria Microcystis aeruginosa [117]. The simultaneous presence of GLY and cyanobacteria increased stress to the microalgae. In addition, impairments in growth rate, macromolecule content, and population dynamics were observed, resulting in increased levels of catalase and glutathione peroxidase due to oxidative stress (≥ 0.74 mg l−1) [117]. Additionally, changes in the external morphology and ultrastructure of microalgae were also demonstrated (e.g., loss of cell wall integrity and typical cell form, differences in starch and polyphosphate granules) [118]. Moreover, the presence of M. aeruginosa increased the damage observed during exposure to GBH [118]. Species-specific and dose-dependent stimulatory effect of GLY were found in several freshwater cyanobacteria species [119]. A strong correlation between reduced phosphonate levels and algal growth was demonstrated. Moreover, the uptake of phosphate was strongly dependent on the GLY concentration [119]. A concentration-dependent decrease in growth and chlorophyll-a content was observed in GLY-exposed M. aeruginosa cells (1–10 mg l−1). Furthermore, increased malondialdehyde levels and antioxidant enzymatic activities (SOD, catalase, peroxidase) were observed (1–2 mg l−1). According to the further results of the study, GLY induced apoptosis in the treated cells and triggered the release of cyanotoxin in M. aeruginosa [120]. After exposure to GLY (6.09 and 0.9 mg l−1), a concentration-dependent growth inhibition was observed in the dinoflagellate Prorocentrum donghaiense. Moreover, P. donghaiense was unable to utilize GLY as a phosphorus source [94]. In an 8-day microcosm study, GLY led to a drastic decrease in the abundance of phycocyanin-rich picocyanobacterial by 85% [121]. Exposure to various GBHs also resulted in reduced abundance of phycocyanin-rich picocyanobacterial [122]. The abundance of phytoplankton was not affected by exposure to GLY-IPA, while increased net total abundance was observed after the exposure to GBHs (Glyphosate II Atanor and Roundup Max) [122].
Under field conditions, a decrease in chl-a was observed in the collected biofilm samples at all GLY concentrations tested (0.25–2.54 g l−1). Furthermore, a dose-dependent decrease in biomass and gross primary production of autotrophs in biofilms was observed [86]. A slight decrease in algal biomass was observed after treatments with both pure GLY (100 μg l−1) and a GBH (Roundup Classic) at the same GLY equivalent concentration in freshwater biofilms grown under natural conditions in Lake Balaton (Hungary) compared to the control [87]. In biofilms grown in the River Danube (Hungary), GLY (100 µg l−1) initially led to a decrease in algal biomass, followed by an increase and a realignment of algal species in the biofilms. GLY-sensitive species were replaced by more tolerant ones (e.g., filamentous green species of algae), leading to a temporary decrease in biomass through various selection processes [87]. Treatment with Roundup Classic (100 µg AI l−1) after 2 weeks also resulted in a decreased algal biomass in biofilms from Lake Balaton and the River Danube, with POEA increasing the toxicity of the GBH [87].
Similar selection processes have been found in natural communities of marine microphytobenthos following treatment with a Roundup GBH [123]. Several studies using standard algal growth inhibition assays [124] and community-level biofilm studies [125, 126] have demonstrated the increased combined toxicity of GLY and the additives in GBHs. At lower concentrations (0.06–29.6 µg l−1), GLY can serve as a source of nutrients and phosphorus for algae species [125, 127]. In addition, GLY can also trigger pathways for protein and metabolite synthesis [108, 128], which can lead to increased biomass growth. The effects of GLY on algal communities in biofilms are highly site-specific and are greatly influenced by the specific environmental characteristics of natural aquatic habitats (e.g., dissolved oxygen content, pH), in addition to various climatic and weather conditions in different years [4, 129]. Most of the effects of GLY (0.4 mg l−1) on freshwater periphyton were reversible after a recovery time of 7 days. In contrast, the higher tested concentration tested (4 mg l−1) caused irreversible changes in the exposed periphyton community based on the applied recovery time of 21 days [130]. Exposure to GLY and GBHs at a much higher concentration (3 mg l−1) increased the proportion of blue-green algae, while the ratio of green algae and diatoms in freshwater periphyton decreased [126]. Furthermore, the periphyton community proved to be much more tolerant to the effects of GLY compared to phytoplankton [131]. The effects of GLY on the composition of benthic diatom communities have also been demonstrated [132]. Furthermore, a higher combined toxicity of GBH formulations (such as Glifosato II Atanor, Roundup Max) was observed compared to the toxicity of technical grade GLY alone [126]. At a lower GLY concentration (10 µg l−1), inhibited growth of the autotrophic community was observed in the exposed natural freshwater biofilm communities. However, no effects on pigment and polysaccharide content or esterase enzyme activity were observed [133]. Additionally, in freshwater biofilms exposed to GLY, even at very low concentration (0.01 mg l−1 GLY-IPA), decreased chlorohyll-a content, photosynthetic efficiency and capacity, and changes in diatom community composition [134]. Although, the toxicity of AMPA and the effects on the activity of antioxidant enzymes were not observed after either GLY or AMPA exposure [134].
The combination of technical-grade GLY or Roundup Max GBH and the presence of the invasive mussel Limnoperna fortunei resulted in antagonistic effects on phytoplankton [135]. The higher level of available nutrients provided by GLY was offset by the filtering activity of mussels and dramatic reductions in pico- and phytoplankton due to mussel grazing [135]. In another study, increased phytoplankton abundance was observed especially for Microcystis species (up to 289% and 639%) after exposure to GLY and a GBH Glifosato Atanor (6 mg AI l−1), respectively. In contrast, the growth of Microcystis species was limited after treatment with Roundup Max [136]. The evenness of the phytoplankton community was also decreased in the exposed groups. However, the presence of L. fortunei significantly increased the evenness of the communities exposed to GLY or GBHs [136]. In addition to herbicides that directly inhibit photosynthesis (e.g., atrazine), other pesticide AIs such as GLY can also affect photosynthetic and respiratory processes through their effects on various metabolic pathways [127, 129]. The adverse effects of GLY on photosynthetic processes can be mainly explained by the direct or indirect inhibition of plastoquinone biosynthesis; quinone compounds are found in chloroplasts, which are crucial electron transport molecules in the light reaction of photosynthesis [137, 138]. Moreover, the decreased chlorophyll concentration [139] can directly affect the rate of electron transport in the chloroplast [129]. After GLY exposure, reactive oxygen species (ROS) generated in mitochondria can also impact photosynthesis by inhibition of the respiratory electron transport chain. Free radicals leave mitochondria and enter the chloroplast, where they cause oxidative damage to the photosynthetic apparatus and decrease photosynthesis activity [139]. The phytotoxic effects of GLY on photosynthesis activity in algae have been observed in several species of green algae and diatoms, resulting in damage to the photochemical efficiency of the PS II photochemical system [140]. In studies testing the effects of a Roundup GBH (0.28–6 mg l−1, the phytotoxicity of GLY on cyanobacterial and green algal species (M. aeruginosa, Nitella microcarpa var. wrightii) was enhanced by the presence of POEA [141] although increased cell density, chl-a content, photosynthetic activity was also observed on algae species at lower concentrations [127], indicating a possible hormetic response that has enhanced stress effects on the plant organism [142].
The effects of GBH co-formulants have been investigated in several studies. The 72-h EC50 values for POEA in P. subcapitata ranged from 0.2 to 4.9 mg l−1 [30, 104, 143]. In contrast, the toxicity of alkyl polyglucosides (APGs) (C12–14) was significantly higher (72-h EC50 = 11–46 mg l−1). Significantly higher 72-h EC50 values of 1113–1543 mg l−1 were observed for APGs with shorter carbon chains (C8–10) [144, 145], indicating correlation between alkyl chain length and increased toxicity.
Effects on aquatic plants
The aquatic macrophyte community serves as a microhabitat for planktonic and periphytic communities, as well as a food source for herbivorous organisms [146, 147]. Thus, observations that GLY can exert numerous detrimental effects on the aquatic macrophyte community leading to damage in food chain networks, is a serious aquatic ecotoxicological concern. The main results of ecotoxicological testing on aquatic plants are summarized in Table 3. In algal and duckweed growth inhibition tests, the inhibitory effect of AMPA on D. subspicatus growth was 1.5-times weaker than for a Roundup GBH. The GBH caused 100% growth inhibition (1.15 mg l−1) in the common duckweed (Lemna minor), even at much lower concentrations compared to the ready-to-use concentration (18.38 mg l−1). AMPA proved to be much less toxic [148]. Furthermore, increased ascorbate peroxidase activity and polyamine levels were observed in L. minor tissues after exposure to a GBH (Roundup Ultra 360 SL), although a concentration-dependent reduction was detected in the pigment content and biomass of duckweeds (≥ 360.5 mg l−1 AI) [149]. Additionally, the accumulation of GLY in tissues of L. minor exposed to 0.68 mg l−1 GLY-IPA, resulted in decreased growth, yield and photochemical activity of the PS II photochemical system. Moreover, inhibition of chl-a, -b, and carotenoid synthesis was also detected, while the peroxidase and catalase activities were increased at 1.6–4.56 mg l−1 GLY-IPA [150]. However, the inhibitory effects of a GBH Taifun Forte were found to be temperature-dependent on L. minor [151]. The inhibitory effect of AMPA was also demonstrated on the growth of L. minor exposed to AMPA (≥ 35 μg l−1) [152]. In addition, a reduced chlorophyll content (30–50 μg l−1) and an altered chlorophyll and amino acid metabolism were detected [152].
In Salvinia molesta exposed to GLY and its metabolite (≥ 40 μg l−1 GLY, ≥ 10 μg l−1 AMPA), reduced photosynthetic rates and pigment contents were observed [153]. In contrast, malondialdehyde levels and enzyme activities (catalase, ascorbate-peroxidase) were increased after GLY and AMPA exposure. In combination, the toxic effects of AMPA and GLY were enhanced. Additionally, the high removal efficiency of S. molesta was also demonstrated for GLY and AMPA (up to 74.2% and 71.3%, respectively) [153]. GLY (≥ 0.05 mg l−1) caused growth inhibition in the submerged macrophyte Vallisneria natans, while the growth of Acorus calamus was impaired at the higher GLY concentrations tested (≥ 5 mg l−1) [116]. Exposure to AMPA caused growth inhibition and increased malonaldehyde levels only at the highest concentration tested (≥ 50 mg l−1). Compared to A. calamus, V. natans was more sensitive to AMPA-induced oxidative damage [116]. The combined effects of GLY and AMPA were concentration dependent and species-specific on plant growth and oxidative stress parameters [116]. In the aquatic macrophyte Egeria densa, decreased photosynthetic rates and chl-a content were observed after exposure to a Roundup GBH (0.28–6 mg l−1) and AMPA (0.03 mg l−1), while dark respiration rates increased after exposure [154].
Effects on aquatic invertebrates
The main effects of GLY and GBHs on aquatic invertebrates are presented below according to the classification of animals based on phylogenetic systematics [155]. Thus, we start with hydra, arthropods and rotifers (including zooplankton species, crabs and insects), followed by aquatic snails and mussels belonging to the phylum of mollusks, and finally with the other specialized species such as trematodes and Echinodermata.
Effects on hydra, arthropods and rotifers
Cnidarian species, including Hydra viridissima, are increasingly used as sensitive test organisms in ecotoxicological studies due to their small body size, simple anatomy, and ease of culture maintenance [156,157,158]. Morphological alterations were detected in H. viridissima exposed to GLY and the GBH Roundup Ready at a concentration of 5.2 mg l−1 (AI equivalent) [159]. After exposure, a high recovery capacity was observed in hydras exposed to GLY (95%). In contrast, no recovery of hydras was observed after GBH treatment [159]. Adverse effects on reproduction were indicated also after GBH exposure [159].
Zooplankton in aquatic ecosystems includes planktonic crustaceans and rotifers. This subchapter also examines scientific results for crustaceans and insects whose life cycle can be linked to aquatic environments (Table 4). Planktonic crustaceans, such as species of the genus Daphnia, which belong to the filter-feeding organisms, play a crucial role in aquatic ecosystems and food webs. Furthermore, due to their sensitivity to changes in water quality, daphnids are an excellent indicator species in aquatic ecotoxicology tests [160]. However, significant differences in the sensitivity of different crustaceans are occasionally observed. These differences in sensitivity can be observed in taxonomically related species such as the common water flea (Daphnia pulex and Ceriodaphnia dubia) and the great water flea (D. magna), although they have similar feeding strategies and lifestyles [79, 161]. In ecotoxicology tests of D. magna with GLY, significant differences were found, with acute toxicity (EC50) values ranging from 4.2 to 24 mg l−1 [100, 162,163,164,165] and on occasion reaching as high as 146–930 mg l−1 [111, 166,167,168].
Similarly, reported EC50 values for GBHs exhibit significant variability, ranging from 1.75 to 782 mg l−1 [168,169,170,171]. These observed differences in EC50 values can be explained by variations in AI content, the presence of different co-formulants in GBHs tested, differing sensitivity between D. magna strains and different experimental conditions such as pH, dissolved oxygen content, or temperature. Several studies have demonstrated increased toxicity of GBHs containing POEA as a co-formulant, compared to toxicity observed with GLY alone [100, 172, 173]. However, one study found slightly lower acute toxicity of a GBH compared to GLY-IPA alone [174]. The effects of Roundup on immobility and hydrolytic enzyme activities proved to be temperature-dependent based on acute toxicity testing on D. magna [175]. Exposure of D. magna to GLY resulted in down-regulation of the Cyp4 gene (190 mg l−1), while expression of Cyp314 remained unaffected, suggesting harmful effects on steroid and fatty acid metabolism. Additionally, vitellogenin, which is responsive to the estrogenic effect, was not affected [176]. GLY and GBH formulations caused a decrease in body size and growth of D. magna juveniles even at the lowest tested concentrations of GLY-IPA and a Roundup GBH (0.05 mg AI l−1). Moreover, additional negative impacts were detected on reproduction rates [174]. At higher concentrations (> 20 mg AI l−1), GBHs impaired the survival of D. magna and Cyclops vicinus, with observed morphological alterations in both test organisms [177]. The temperature-dependent toxicity of a Roundup GBH on alkaline phosphatase activity was also demonstrated in D. magna. Based on the observed results, alkaline phosphatase activity whilst playing an important role in digestion, proved to be an appropriate biomarker of damage to D. magna [172, 178]. Multigenerational ecotoxicology tests with a binary mixture of GLY and silver nanoparticles did not clearly demonstrate interactions between these substances [173]. However, the combined chronic multigenerational effects related to reproductive parameters (e.g., delay in the age at first brood) indicated increased toxicity compared to GLY and silver nanoparticles individually [173].
When evaluating the effects of the Sulfosato Touchdown on 30 zooplankton taxa was undertaken, a reduction in species diversity was observed above 2.7 mg l−1 [179]. Altered diversity, including a decrease in the proportion of cladocerans and an increase in rotifers (Bdelloidea), was observed in all GLY treatment groups. Additionally, treatment with this herbicide exhibited a selective impact on zooplankton hatching dynamics, including timing of first hatch and frequency of hatch [179]. Indirect effects of GBH Glifosato Atanor (3.5 mg AI l−1) on zooplankton were shown with the significant increase in the abundance of rotifer species Lecane spp. [180]. The observed effects can be explained by the improved food availability provided by the higher abundance of picocyanobacterial and bacteria after exposure [180]. Multi- and transgenerational effects of GLY have been demonstrated in the estuarine rotifer Proales similis after exposure to GLY even at very low concentration (1 µg l−1) [181]. In another study, sublethal exposure to a Roundup GBH resulted in a dose-dependent disruption of molting and development, as well as carbohydrate and energy metabolism in a saltwater crustacean, Artemia franciscana [182]. A complete inhibition of hatching was observed in GBH-exposed Artemia salina (144–288 μg AI ml−1) [183]. In addition, altered early development and increased catalase activity (≥ 0.72 μg AI ml−1) were also detected. The observed effects can be associated with excessive ROS levels and indicate the possible teratogenicity of the Roundup formulation [183].
Based on the results of ecotoxicological testing of POEA, the average 96-h EC50 value determined for Daphnia species (D. magna and D. pulex) was found to range from 0.1 to 3.8 mg l−1 [111, 184]. When studying the effects of GBHs, POEA was identified as the most toxic component [185]. Adverse effects of non-ionic APGs were demonstrated on D. magna in the concentration range of 2.5–5 mg l−1 [186]. Additionally, increased toxicity was observed with longer alkyl chain lengths of APGs [145].
When determining the acute effects of a Roundup GBH on the shrimp Caridina nilotica and its three life stages (neonates, juveniles, adults), it was found that neonates were more sensitive to the effects of the GBH at a much lower concentration (average 96-h LC50 = 2.5 mg AI l−1). Behavioral abnormalities, such as slow, uncoordinated and erratic movements were also observed at all life stages [187]. Adverse effects of GLY (0.02 and 1 mg l−1) and a GBH (Roundup UltraMax; 0.01 and 0.2 mg AI l−1), were found on body weight gain, reabsorbed vitellogenic oocytes, vitellogenin content in the ovary of an estuarine crab (Neohelice granulata). The inhibition of ovarian protein synthesis was detected after the exposure to the tested GBH (0.2 mg AI l−1), but GSI and HIS index were not affected [188, 189]. Furthermore, the adverse effects of a GBH on immune status, spermatophore morphology, spermatogenesis and spermatozoa quality of the Chinese mitten crab (Eriocheir sinensis) were demonstrated [190, 191].
Low GLY concentrations were found to cause delayed hatching of females and rapid hatching of males in exposed midge larvae (Chironomus xanthus), showing negative effects at environmentally relevant concentrations (0.7 mg l−1) on growth and development [192]. However, the analysis of macroinvertebrates (e.g., Chironomidae) did not show any effects on the diversity and abundance of macroinvertebrates after exposure to the GBH Roundup [193]. The toxicity of a Roundup GBH was higher compared to the effects of the AI on the growth rate, behavior and most physiological endpoints (e.g., escape swimming speed, food intake, fat storage) of the damselfly (Coenagrion pulchellum). However, some negative effects (e.g., changes in survival, muscle mass, sugar and total energy content) were observed only at the higher concentrations tested (2 mg l−1 GLY). These results confirm the negative effects of the POEA co-formulant on mortality and fitness of C. pulchellum by affecting population dynamics and predation. However, based on the results obtained, the toxic effects of the Roundup cannot be completely attributed to the presence of the surfactant [194].
Effects on mussels
Low mortality, and only few toxic effects of Roundup Express GBH and POEA on juvenile oysters (Crassostrea gigas) were observed at subchronic exposure (35 days) at low concentrations (≥ 0.1 µg l−1) based on different parameters (e.g., shell length) [195]. However, GBHs, GLY and AMPA had no effects on embryo-larval development in C. gigas in the concentration range of 0.1–1000 μg l−1 compared to controls. Above this concentration range, a concentration dependence was observed in the severity of the detected abnormalities. Metamorphosis assays showed higher toxicity for GBHs than for GLY and AMPA [196]. After the dietary exposure to a GBH (Scenedesmus vacuolatus green algae exposed to Glifosato Atanor at concentration of 6 mg AI l−1 with the addition of 2.5% alkyl aryl polyglycol ether surfactant, biochemical alterations were detected on Limnoperna fortunei. A significant decrease in the carboxylesterases, while increased activity of GST and alkaline phosphatase were demonstrated. Effects on several enzyme activities (e.g., catalase, AChE, and superoxide dismutase) or oxidative damage to proteins and lipids were not proved [80]. GLY impaired acetylcholinesterase (AChE) activity and hemocyte parameters in the mussel Mytilus galloprovincialis due to damage to important biological processes such as endoplasmic reticulum function, energy metabolism, cell signaling, and Ca2+ homeostasis (≥ 10 µg l−1), although no effects on antioxidant enzyme activity were observed [197, 198]. At very low concentrations (0.1 µg l−1), GLY and AMPA elicited cytoprotective responses in hemocytes from treated M. galloprovincialis [199]. These observations appear to be due to altered efflux activity of multi-xenobiotic resistance (MXR) and altered expression of the Abcb gene encoding an MXR-related ABC transporter P-glycoprotein. Simultaneous exposure to GLY and AMPA induced enhanced responses in addition to the decreased efflux activity with Abcb down-regulation (at 1 µg l−1 GLY/AMPA exposure) [199]. Inhibition of AChE was detected in the mussel Perna perna after GLY exposure (IC50 = 104.8 mg l−1) [200]. The studied mussel appeared to be much more sensitive than zebrafish (Danio rerio) and the onesided livebearer (Jenynsia multidentate) [200]. GLY and AMPA exposures (100 µg l−1) indicate changes in the physiological homeostasis of M. galloprovincialis with the findings suggesting that the tested compounds may damage the animal’s microbiota. AMPA caused only a slight change in the microbial community of the exposed mussels, but substantial modifications were observed after exposure to GLY and the mixture of GLY and AMPA [201]. A study of another POEA surfactant, Genamin T-200, demonstrated high toxicity on C. gigas embryo larval development (EC50 = 262 µg l−1) and metamorphosis (EC50 = 3,027 µg l−1) [202]. The most important results of the aquatic ecotoxicology tests on mussels are summarized in Table 5.
Effects on aquatic snails
The acute toxicity of GLY was demonstrated in the invasive snail Pomacea canaliculate, but only at high concentrations (96-h LC50 = 175 mg l−1) [203]. Long-term exposure at sublethal concentrations (20 and 120 mg l−1) resulted in inhibition of food intake, changes in metabolic profile (e.g., enhanced overall metabolic rate and modified catabolism from protein to carbohydrate/lipid mode), and impaired growth performance. In addition, increased growth was observed at 2 mg l−1. Cellular responses in enzyme activities indicated increased tolerance of exposed snails by their defense system against the harmful effects of oxidative stress induced by GLY [203]. After 21 days of exposure, the effects of GLY (200 µg l−1) on fatty acid composition and glutathione peroxidase activity in freshwater gastropods (Lymnaea sp.), were strongly dependent on temperature (20 °C and 25 °C). In addition, increased glutathione-S-transferase (GST) activity was observed in GLY-exposed snails, indicating the essential role of GST in the detoxification processes [204]. A Roundup GBH caused changes in mortality, reproduction, and development of Lymnaea palustris aquatic snails while acute steroid regulatory protein levels decreased upon treatment with the GBH, as well as after chronic exposure to GLY (3.5 mg l−1) and a GBH (19.5 mg l−1). Furthermore, lower testosterone and higher or equal estradiol levels were observed in snails after GLY exposure of 3.5 mg l−1 compared to untreated controls [205].
The co-formulant POEA in surfactant MON 0818, which is added to many commercial GBH formulations, did not significantly affect the viability of eggs of the snail Planorbella pilsbryi up to 9.9 mg l−1 [206]. However, juveniles (LC50 = 4.0 mg l−1) were more sensitive than adults (LC50 = 4.9–9.1 mg l−1), and egg laying was inhibited by the co-formulant (EC50 = 0.4–2.0 mg l−1). This inhibitory effect was restored in clean water after the 96-h exposure up to 4.9 mg l−1. Additionally, visible damage to tentacles of adult snails was observed at concentrations ≥ 2.7 mg l−1 [206]. Based on the results, environmentally relevant concentrations of GLY and surfactants (e.g., MON 0818) may pose a risk to populations of aquatic snails (Table 6).
Effects on trematodes and Echinodermata
In the natural environment, the GBH Roundup may affect the transmission dynamics and development of trematodes (Echinostoma paraensei) whose life cycle is associated with water courses [207]. In a study of the developmental and metabolic effects of GLY, a GBH (Roundup Power 2.0), and AMPA at environmentally relevant concentrations (1–100 µg l−1) on larval sea urchin (Paracentrotus lividus), the observed effects were highly dependent on the type and the concentration of the tested compounds according to the parameters measured [208]. In general, GLY and AMPA showed similar levels of toxicity to the sea urchin, while the GBH formulation was less toxic than the GLY [208]. The main results of ecotoxicological tests on trematode and Echinodermata species are also listed in Table 6.
Effects on aquatic vertebrates
Similar to the adverse effects observed in aquatic invertebrates, GLY and the various components in GBHs may also negatively impact the health of aquatic vertebrates, such as various reptiles, fish, and amphibian species. The potential routes of exposure to aquatic contaminants may be different for these species. However, the number of ecotoxicological studies examining the effects of GLY and GBHs on reptiles is small. In aquatic turtle species (Trachemys scripta elegans and Mauremys leprosa) GBH Clinic (30 mg AI l−1) significantly increased catalase and superoxide dismutase (SOD) activities of the enzymes, while reduced AChE activity was observed after the 96-h exposure. Effects on lipid peroxidation were not demonstrated [209]. In Pelodiscus sinensis turtles exposed to GLY-isopropylammonium (0.02–20 mg l−1), no effects were observed on growth or functional performance, including food intake and swimming speed, or on liver antioxidant responses (e.g., catalase and SOD enzyme activity) and gut microbial diversity [210].
However, perturbations in hepatic metabolite profiles were detected, mainly affecting amino acid metabolism in exposed animals [210]. Exposure to a Roundup GBH (11 or 21 mg l−1) altered immune parameters and complement system activity, as well as decreased white blood cell numbers and negatively affected growth were indicated in the broad-snouted caiman (Caiman latirostris), while total protein content was increased in the exposed animals [211, 212]. The main results of ecotoxicological studies on reptiles are summarized in Table 7.
Effects on fish species
Various fish species living in different aquatic habitats are highly exposed to chemical contaminants from industry. Contact with xenobiotics (e.g., GLY) in water is unavoidable throughout all stages of development and their life cycle. Moreover, fish species can absorb and concentrate various aquatic pollutants, which can result in food safety risks for human consumers [213]. The effects on fish observed during ecotoxicological tests are summarized in Table 8. A 24-h exposure to a Roundup GBH (10 mg l−1) resulted in decreased SOD and glutathione peroxidase activity, while glutathione levels and the GST activity increased in the liver of the streaked prochilod Prochilodus lineatus, indicating oxidative stress [214]. AChE activity was inhibited in the brain after 96 h and in muscle after 24 h of exposure. Therefore, acute exposure to the Roundup impaired antioxidant defenses, leading to the occurrence of lipid peroxidation [214]. Reduced GST levels were observed in the South American catfish (Rhamdia quelen) exposed to lower Roundup GBH concentrations (≥ 0.45 mg l−1) [215]. During the recovery period, increased GST activity was detected as a possible compensatory response, although catalase and SOD activity decreased, indicating toxicity from the GBH. Oxidative stress was detected during Roundup exposure possibly caused by increased protein carbonyl content and lipid peroxidation (≥ 0.45 mg l−1) [215]. Increased ROS levels and cell death were observed in zebrafish (D. rerio) larvae exposed to Roundup Flex GBH (10 µg AI ml−1) for 4 h 30 min [216]. After 14 days of exposure to GLY and a Roundup GBH at relatively low concentrations (0.01, 0.5, and 10 mg a.e. GLY l−1), upregulation of the antioxidant system was observed in brown trout (Salmo trutta). Additionally, significant changes in the expression of transcripts encoding components of the antioxidant system, a number of stress-response proteins, and pro-apoptotic signaling molecules were observed even at the lowest dose, consistent with a cellular response to oxidative stress as the most significant mechanism of toxicity of both GLY and its Roundup formulation [84]. The effects of GLY (2.5 and 5 mg l−1 for 120 h) on oxidative stress enzyme activity and malondialdehyde concentration as a marker of lipid peroxidation were detected in goldfish (Carassius auratus) [217]. In addition, the effects on various parameters of oxidative stress and lipid peroxidation (e.g., level of thiobarbituric acid, activity of GST and SOD) were age-specific in killifish (Cynopoecilus sp.) exposed to Roundup Original (65–260 µg AI l−1) [218].
A slight decrease in the number of erythrocytes, as well as hemoglobin and hematocrit levels were also observed compared to controls, indicating moderate anemia in the exposed goldfish [217]. In guppy (Poecilia reticulata) gill erythrocyte cells exposed to different concentrations of Roundup Transorb GBH (0.91–3.66 mg l−1) for 24 h, a concentration-dependent increase in the number of damaged cells was observed, indicating mutagenic and genotoxic effects [219]. Genotoxic effects of another GBH (Roundup Full II—2.75 mg l−1) were detected in the blood, liver and gill cells of exposed pacu fish (Piaratus mesopotamicus) [220]. The genotoxic potential of GLY, Roundup, and POEA was detected in blood cells of the exposed European eel (Anguilla anguilla) [221]. Altered hematological and biochemical parameters (e.g., decreased level of alkaline phosphatase, hemoglobin and hematocrit value, increased level of white blood cells) were also observed in Labeo rohita after chronic exposure to GBH Roundup (0.63–2.06 mg l−1) [222].
Lower heart rates were observed in treated D. rerio embryos (100 and 1000 µg l−1 of GLY at 48 h), indicating possible cardiotoxicity [223]. Altered transcriptome profiles (30 differentially expressed genes involved in metabolic processes, oocyte maturation, and nervous system development) were also observed in these embryos at the higher GLY concentration after 96 h [223]. The cardiovascular toxicity of GLY was also demonstrated in D. rerio embryos exposed to 30–120 μg ml−1 GLY up to 72 h after fertilization [224]. Cardiac malformations, including enlarged chambers, rhythm alterations, and thinned ventricular walls, as well as a defective intersegmental vasculature indicative of damaged angiogenesis, were observed in the exposed embryos. The cardiovascular effects of GLY might be related to apoptosis, as apoptosis occurs in the cardiac and vascular regions. Additionally, altered development, hatching abnormalities, mortality, and decreased body length of exposed embryos were also observed [224]. Exposure to GLY and Roundup Original DI (250–1000 µg l−1) caused decreased heart rate and decreased activity of GST and AChE in exposed D. rerio embryos [225]. Effects on behavior and various biochemical parameters (e.g., total antioxidant capacity, lipid peroxidation, ROS level) were not observed. A higher rate of malformations (e.g., pericardial edema, yolk sac edema, and curvature of the spine) was observed in GBH-exposed embryos [225].
When tambaqui (Colossoma macropomum) were exposed to Roundup GBH (10 and 15 mg AI l−1), altered biotransformation processes were observed in the gills [226]. In addition, ROS were produced in the liver and increased DNA damage was observed in red blood cells. Furthermore, inhibition of AChE activity was also observed in the exposed fish brain [226]. Concentration-dependent DNA damage and increased levels of ROS and lipid peroxidation were observed in the spotted snakehead (Channa punctatus) exposed to sublethal GLY concentrations (Roundup 3.25–6.51 mg AI l−1). However, the extent of lipid peroxidation and DNA damage was higher in gills than in blood cells [227].
Sex-specific disruption of the hepatic metabolism in zebrafish (D. rerio) was detected after the longer-term exposure (28 days) at a lower GLY concentration (700 µg l−1). In females, decreased uridine 5’-monophosphate content was observed in the pyrimidine metabolic pathway, as well as the reduction of purine intermediates was indicated. In addition, decreased aminoadipic acid in the lysine degradation pathway observed in males [228]. GLY exposure also resulted in increased stress responses in both sexes, namely an increased stress-inflammatory response in females and an impaired oxidative stress response in males [228]. Exposure to GLY (35 mg l−1) caused decreased triiodothyronine (T3)/thyroxine (T4) ratios in exposed D. rerio embryos (120 h post-fertilization) [229]. Moreover, abnormal expression patterns of genes related to the hypothalamic-pituitary-thyroid and growth hormone/insulin-like growth factor axes were observed. As a result, developmental toxicity was demonstrated in these fish (e.g., reduced heartbeats, premature hatching, shortened body, swim bladder deficiency, pericardial and yolk sac edema) (≥ 7 mg l−1). No oxidative stress or significant malformations were detected at the lowest concentration, but hormonal changes were observed. GLY at 7 and 35 mg l−1 caused accumulation of ROS in larvae [229]. In vivo, the estrogenicity of AMPA, GLY and GBHs was demonstated in an estrogen-sensitive, transgenic zebrafish line after 120 h of exposure (0.35–2.8 mg l−1) [230]. The acute toxicity of AMPA was not detected, while the toxicity of GBHs was higher compared to GLY. In addition, sublethal anomalies and malformations were observed in the GBH-exposed embryos [230].
Oxidative DNA damage and production of ROS was observed in juvenile common carp (Cyprinus carpio) (≥ 5 mg l−1). Liver inflammation in vivo, accompanied by oxidative damage and altered physical intestinal barrier, was observed in carp exposed to GLY concentrations (5–15 mg l−1) for 30 days. Moreover, at 15 mg l−1 GLY, inhibition of AChE activity in the brain of the fish was observed, and decreased swimming speed and distance, as well as average acceleration were demonstrated [231]. In addition, also oxidative DNA damage, ROS production, mitochondrial dysfunction, and reduced cell viability were detected on the tested fish cell line (0.65 and 3.35 mg l−1) [231]. In another study, an increased frequency of nuclear morphological abnormalities and micronuclei formation were observed in D. rerio exposed to GLY (1, 65, and 5000 µg l-1 for 72 h) [232].
After the common carp (C. carpio) and zebrafish (D. rerio) were exposed to GLY at various concentrations (0.005–50 mg l−1) at early life stages, a delay in hatching was observed, especially at the highest concentration after 72, 96, and 120 h post fertilization. In contrast, hatching stimulation was observed in D. rerio embryos exposed to GLY (96 h post fertilization). Early life stages of C. carpio were more sensitive, with numerous malformations and delayed development compared to D. rerio. GLY at lower concentrations (0.005 mg l−1) resulted in significant changes in both fish species, including altered mortality and occurrence of malformations, possibly reducing biodiversity [81]. Long-term exposure to low concentrations of GLY (65 μg l−1 for 15 days) showed adverse effects on reproduction in D. rerio, with a significant increase in oocyte diameter associated with the appearance of concentric membranes resembling myelin-like structures in the ultrastructure of ovaries correlating with the outer membranes of mitochondria and with yolk granules [233]. Low concentrations of GLY and AMPA (≥ 10 ng ml−1) caused developmental toxicity in zebrafish embryos (exposure from 2 to 74 h post-fertilization for 72 h), with concentration-dependent heart rate elevation and arrhythmia observed [234]. In exposed embryos, disturbances in heart development were observed, possibly related to altered transcription levels of genes involved in development and apoptosis. Pericardial edema and bone deformities were also observed as a possible consequence of inhibition of Na+/K+-ATPase and Ca2+-ATPase after GLY and AMPA exposure (≥ 1 ng ml−1) [234].
Reproduction of D. rerio was affected by 21-day exposure to GLY and GBH Roundup, while GLY (10 mg l−1) caused decreased egg production in breeding colonies, although fertilization rate was not affected. Moreover, both Roundup and GLY (10 mg l−1) increased mortality and premature hatching of early-stage embryos [235]. In the one-sided livebearer (J. multidentata) concentration-dependent histological changes were observed in the gills and liver after the exposure to Roundup (≥ 0.5 mg l−1). In addition, the number of copulations and mating success decreased in male fish [236]. Adverse effects of GLY (5 and 10 mg l−1) on sperm quality of D. rerio were observed after 24 and 96-h exposure, including damage to sperm membranes and DNA. Moreover, reduced mitochondrial function and sperm motility were detected, suggesting reduced fertility (≥ 5 mg l−1) [237]. In D. rerio embryos exposed to GBH (1–100 mg AI l−1) for 24 to 96 h, a dose-dependent inhibition of carbonic anhydrase activity was observed, which was attributed to the production of ROS, especially in branchial regions, caused by cellular apoptosis [238].
Various types of malformations were also observed in a dose-dependent manner, including pericardial edema, spinal curvature, yolk sac edema, and body malformation (≥ 1 mg AI l−1) [238]. Furthermore, a negative effect of Roundup GBH (78 µg AI l−1) on the concentration of 17β-estradiol and reduced glutathione concentration was observed in the liver of male delta smelts (Hypomesus transpacificus) (700 µg AI l−1) [239]. Decreased body weight, altered morphology (24 h post-fertilization), survival rate, growth, and behavioral parameters were demonstrated in Clarias gariepinus exposed to the GBH Forceup (0–1 mg l−1) at different developmental stages (e.g., gametes, postfryer, juvenile) [240]. Moreover, increased levels of malondialdehyde were detected at the higher GBH concentrations indicating an oxidative stress response after GBH exposure. Decreased levels of reduced glutathione and SOD activity were found in exposed post-fingerlings and juveniles compared to controls. Histological analysis revealed necrosis in the gills, cardiac myocytes, brain, and liver of exposed fish [240].
After daily exposure of the rainbow trout (Oncorhynchus mykiss) to 1 μg l−1 GLY and GBHs (Roundup Innovert and Viaglif Jardin) for 10 months during spawning, no effects on average body weight, relative fecundity, and fertility were observed [241]. However, fish exposed to the GBH Viaglif Jardin two months before spawning showed a 70% decrease in the proportion of macrophages and a 35% decrease in phagocytic activity. One month after spawning, a lower tumor necrosis factor-α level was observed, but the difference was not significant compared to the control [241]. No effects on locomotor activity, somatic indexes, AChE and catalase activity were demonstrated in adult females of the ten spotted live-bearer (Cnesterodon decemmaculatus) exposed to GBH Roundup Max (0.2 and 2 mg l−1) for 6 weeks. However, the activity of GST in liver, reduced aspartate aminotransferase, and alanine aminotransferase were significantly affected in the exposed fish [242]. Additionally, GLY at a concentration of 1 mg l−1 acted as a significant AChE inhibitor in C. decemmaculatus [243].
The inhibitory effect of a Roundup GBH (0.5–10.0 mg l−1 for 96 h) on AChE activity was also detected in the brain and muscle of exposed common carp (C. carpio), although AChE activity increased after the recovery period. Moreover, increased levels of thiobarbituric acid reactive species (TBARS) were measured in the brain, indicating oxidative stress [244]. Increased TBARS levels were also found in the silver catfish (R. quelen) exposed to different GBHs (e.g., Orium, Roundup Original, and Biocarb) at concentrations of 2.5 and 5.0 mg l−1 for 96 h. However, the amount of catalase produced in the liver decreased in all treatments [245]. A sex- and tissue-specific histopathological response was observed in the gills and liver of guppies (P. reticulata) exposed to GLY (35 mg l−1) and AMPA (82 mg l−1) for 96 h [246]. Male fish showed more frequent hepatic inflammatory changes and a higher increase in the area of hepatocyte vacuoles compared to female fish exposed to GLY and its metabolite. Male guppies exhibited higher sensitivity than females, particularly in the presence of AMPA [246]. In the hybrid fish surubim (crossbred between two Neotropical catfish species, pintado, Pseudoplatystoma corruscans × cachara, P. reticulatum), exposure to the GBH Roundup Original (≥ 2.25 mg l−1) for 96 h resulted in reduced plasma glucose levels but increased levels in the liver, while lactate levels increased in both plasma and liver and decreased in muscles [247]. In addition to the concentration-dependent and tissue-specific effects of the GBH, plasma cholesterol concentration decreased at all concentrations tested. Moreover, altered behavioral parameters such as ventilatory frequency and swimming activity were observed at higher concentration (≥ 2.25 mg l−1) [247].
Exposure to GLY and a Roundup GBH (0.01–0.5 mg AI l−1), resulted in altered morphology and behavior of D. rerio even at the lowest concentration tested after a 96-h exposure [248]. Adult fish showed reduced exploratory (≥ 0.065 mg AI l−1) and aggressive behavior (≥ 0.01 mg AI l−1). In the exposed larvae, altered exploratory and aversive behavior were also observed (≥ 0.01 mg AI l−1). Impaired memory was observed in adult fish exposed to Roundup (0.5 mg AI l−1), and exposure to GLY (0.5 mg l−1) resulted in reduced ocular distance in larvae [248]. In C. carpio, significant differences were found in the swimming behavior of fish treated with GLY (50, 100, and 150 mg l−1), along with additional clinical signs such as increased movement of the operculum and darkening of the skin. Hyperplasia, hypertrophy, and hyperemia of the gills were also observed [249].
After a 7-week exposure to a range of GLY concentration (25–150 mg l−1), crossbred red tilapia (Oreochromis niloticus × Oreochromis mossambicus) showed differences in growth pattern, hepato-somatic index, and gonado-somatic index with decreased body weight even at the lowest concentration tested [250]. Time-dependent histopathological effects were observed in the gills of guppies exposed to a GBH (1.82 mg AI l−1), with various epithelial and muscle cell types showing progressive, regressive, and vascular disorders [251]. In C. carpio exposed to GLY (5 and 15 mg l−1) for 60 days, a statistically significant decrease mRNA expression of tight-junction genes and inhibition of AChE activity was observed at the higher concentration [252]. In addition, the combination of GLY (15 mg l−1) and polyethylene microplastics (4.5 mg l−1) led to the inhibition of free-swimming behavior of carp [252]. Exposure of tilapia (O. niloticus) to GLY (2 mg l−1) resulted in dramatic changes in gene expressions, with 94 up-regulated and 131 down-regulated genes [253]. Long-term effects of GLY on 21 proteins related to liver metabolic function were also observed, indicating a redox imbalance and dysregulation of metabolism in exposed fish [253]. In an in vitro 3D hepatocyte-kidney co-culture model, GLY (84.5 mg l−1) affected lipid metabolism in Atlantic salmon (Salmo salar) hepatocytes and kidney cells after a 48-h exposure, leading to an increased cholesterol level and down-regulation of clusterin, which may affect the stability of the kidney cell membrane [254].
Mortality, hatch success, development, and ROS production were not affected by GLY and AMPA (neither individually nor in combination) in exposed D. rerio embryos l-1arvae 7 days after fertilization compared to controls [255]. However, the activity of tested enzymes (e.g., SOD) was altered in a concentration- and a compound-specific manner. Hyperactivity was detected in fish treated with GLY but not AMPA or mixture [255]. Nile tilapia (O. niloticus) exposed to GLY (0.6 mg l−1) for 4 weeks indicated immunosuppression, an oxidative stress response, as well as liver and kidney dysfunction, as indicated by increased levels of glucose, cortisol, and enzyme activities (aspartate aminotransferase and alanine aminotransferase) in gills and other tissue samples [256]. The use of ginger in the feed showed a protective role by enhancing antioxidant and immunological responses in the exposed fish [256]. GLY (1, 5, and 10 mg l−1), affected the energy metabolism and feeding behavior of D. rerio larvae leading to increased mortality [257]. The dynamics between zooplankton and fish larvae were severely affected by GLY, resulting in reduced survival and feeding rates. GLY was also found to bioaccumulate in zooplankton species, with levels up to 6.26% of the total weight of rotifers [257].
In juvenile P. lineatus, exposure to the GBH co-formulant POEA (0.15, 0.75, and 1.5 mg l−1) resulted in increased plasma lactate levels and decreased hepatic catalase activity, red blood cell counts and hemoglobin content [258]. Additional effects included DNA damage, lipid peroxidation and hemolysis but with hematocrit levels not affected [258]. POEA (9.3 and 18.6 µg l−1) was found to induce genotoxic effects in the European eel (A. anguilla) causing higher levels of DNA damage compared to GLY and a Roundup GBH. There was also a synergistic interaction between POEA and GLY in promoting non-specific DNA damage [221]. While no acute toxic effects of GLY and AMPA were observed on D. rerio embryos, significant lethal effects were detected after exposure to the GBH Atanor 48 and POEA. All tested compounds were found to be genotoxic based on Comet assays performed on zebrafish larval cells and rainbow trout gonad-2 (RTG-2) cells. Specifically, POEA induced DNA damage in RTG-2 cells in vivo, implying that it has direct genotoxic properties [259]. The different aquatic ecotoxicological studies demonstrated wide range of the possible side effects of GBHs and their components. The detected effects were indicated even at concentrations lower than environmentally relevant GLY levels (≥ 0.01 mg l−1). However, in several cases the effects are only seen at much higher concentrations. Based on the results, fish proved to be an excellent test organism for many endpoints such as DNA damage, oxidative stress, or the immune response (Table 8).
Effects on amphibians
Several studies have shown that GBHs at concentrations present and measured in the environment have adverse effects on amphibians (Table 9). The direct toxicity of GLY is often associated with higher doses or possibly the presence of GBH co-formulants. Lower concentrations of GLY have effects on tadpole development and behavior. The effects on amphibians are highly depend on the type and composition of GBHs and the sensitivity of different taxa and life stages. However, it is very difficult to determine applicable and valid environmental concentrations of GLY that occur in and affect amphibian habitats. Furthermore, little is known about the environmental concentrations of co-formulants in GBHs [260].
POEA, which has been banned as a co-formulant in GBHs in the EU since 2016 but is still widely used in the USA, is also toxic to the aquatic environment and amphibians due to its ability to disrupt membrane transport and act as a narcotic [261]. The toxic effects of GBHs on amphibians are often much higher than the toxicity of GLY alone. The toxicity of GLY and GBHs to amphibians and reptiles was also considered in EFSA’s official scientific opinion on the risk assessment of commercial pesticide formulations [262]. Amphibians are a very specific group of animals that may be exposed to the effects of GLY and its commercial formulations in both aquatic and terrestrial habitats at different life stages, with amphibian reproduction generally dependent on and associated with water.
Chronic exposure to the GBH VisionMax (0.021–2.9 mg AI l−1) decreased the number of wood frog (Lithobates sylvaticus) tadpoles that reached the metamorphic peak under laboratory conditions [263]. In addition, a concentration-dependent increase in thyroid hormone receptor β was observed in the brain of exposed tadpoles [263]. Not only the GBH Roundup Ultramax (≥ 0.37 mg a.e. GLY l−1), but also GLY (≥ 15 mg l−1) caused liver damage in neotropical frog (Leptodactylus latrans) tadpoles at concentrations frequently found in the environment [82]. Cytotoxic effects of a GBH mixture (Roundup SL and surfactant Cosmoflux 411F) have been demonstrated in various in vitro (at concentrations from 95 µg a.e. GLY ml−1) and in in vivo (at application rates above 5.4 µg a.e. GLY cm−2) tests on Antilles coqui Eleutherodactylus johnstonei erythrocytes with a dose-dependent induction of DNA breaks [264]. Exposure to a sublethal concentration of GLY (1 mg l−1) and GBHs (Roundup Original and Roundup Transorb at 1 mg a.e. GLY l−1) caused skin changes and altered respiratory function in bullfrog (Lithobates catesbeianus) tadpoles [265]. Differences can be observed in the effects of the GBH formulations compared to the effects of GLY alone, and even differences can be observed in the toxicity of the GBHs [265]. In the African clawed frog (Xenopus laevis), severe adverse effects on melanosome aggregation were observed at low concentrations (116.4 mg l−1) of GLY-IPA compared to treatment with a Roundup GBH [266]. The effects of GLY were pH dependent, in contrast to the effects of the formulation. Roundup affected the morphology, cytoskeletal integrity, and intracellular transport of melanosomes in the exposed animals [266]. A study conducted on the common toad (Bufo bufo) exposed to a GBH (Roundup LB Plus at 0.5, 1.0, or 1.5 mg a.e. GLY l−1) at two different temperatures (15 °C or 20 °C) and life stages (eggs or tadpoles) found that eggs were more sensitive compared to tadpoles [267]. More pronounced toxicity of GBH, particularly on egg development, was observed at the lower temperature which may be due to interactive effects of the factors tested. Exposure of eggs to GBH resulted in an average 31% increase in tail, body, and total length compared to controls. Effects on mortality, development, or morphology were not observed in the exposed tadpoles [267]. The effects of the GBH Roundup PowerFlex (1.5–4 mg AI l−1) were studied on the larval development of B. bufo exposed in different life stages (eggs or tadpoles) were studied at two different temperatures (15 °C and 20 °C). Exposure of eggs resulted in significantly increased tail and body length, but only at the lower test temperature [115]. No effects were observed on mortality, body weight, and condition of the exposed tadpoles. Nevertheless, significant interactions between GBH and temperature on tadpole developement, larval tail length, body length and width were observed [115]. Additionally, strong adverse effects of AMPA at early developmental stages (0.4 μg l−1) were detected toads [268]. Moreover, altered hatchling morphology, increased embryonic mortality and longer development duration in Bufo spinosus were observed following exposure to AMPA (0.07–0.39 μg l−1) [269].
Roundup Original MAX (with POEA as a co-formulant) resulted in morphological changes in tadpoles of Northern leopard frog (Lithobates pipiens), wood frog (L. sylvaticus), and American toad (Bufo americanus) [270]. Frog tadpoles exhibited relatively deeper tails, and the presence of predators reduced the mortality observed in the presence of Roundup Original MAX because the herbicide induced antipredator morphology [270].
Exposure to pure GLY (100–0000 µg g−1) caused morphological changes in the liver of the oven frog (Leptodactylus latinasus) [271]. GLY increased the melanin area in liver melanomacrophages, altered the presence of hepatic catabolism pigments into melanomacrophages, and also caused abnormalities of blood erythrocyte nuclei [271]. In addition to lethal effects, shorter body length and lower body weight were observed in tadpoles of native South American frogs (Physalaemus cuvieri and P. gracilis) exposed to the GBH Roundup Original DI (≥ 500 μg a.e. GLY l−1) [272]. Growth and development of L. latrans were affected by GLY (3–300 mg l−1) and its formulation a Roundup GBH (0.0007–9.62 mg a.e. GLY l−1). Oral abnormalities and edema were observed after exposure to both substances, while swimming activity was altered only by Roundup treatment at the earlier developmental stage of tadpoles [273]. At earlier life stages of tadpole development, X. laevis showed higher sensitivity to the toxic effects of GBHs, such as Roundup formulations, with the pre-metamorphic stage being the most sensitive [274]. GLY had no developmental or lethal effects on X. laevis embryos and tadpoles up to 500 mg l−1, whereas the GBH Roundup Star adversely affected embryos and tadpoles even at much lower concentrations (≥ 31 mg AI l−1) [275]. Exposure to sublethal concentrations of the GBH Roundup LB Plus resulted in decreased body length and mobility of X. laevis larvae (≥ 97 mg l−1) [276]. This GBH also impacted heart development, including decreased heart rate and atrium size (≥ 97 mg l−1). Additionally, smaller eyes, cranial cartilages, brains, and shorter cranial nerves were observed after treatment (≥ 121.5 mg l−1) [276]. A significant decrease in body mass of X. laevis metamorphs was observed after exposure to GBHs (Kilo Max and Enviro). Kilo Max (280 mg l−1) altered the sex ratio of exposed frogs (68:32–F:M) compared to controls (50:50). Reproductive malformations, such as translucence, mixed sex, and aplasia, were also observed [277].
Lethal and genotoxic effects of Roundup were observed in the South Asian frog species Euflictis cyanophlyctis, with observed effects increasing in the presence of predation stress [278]. Sublethal and teratogenic effects of the GBH Roundup Power 2.0 were observed in embryos of X. laevis, while a dose-dependent abnormal phenotype, including microphthalmia craniofacial alterations, arrow eyes, and forebrain regionalization defects, was induced after treatment, which can be explained by GLY penetration facilitated by the surfactant co-formulants (1–25 mg a.e. GLY l−1) [279]. Additionally, cardiac malformations were indicated after GLY exposure (≥ 30 mg l−1) [279]. Minor differences in the sensitivity of the tropical frog species studied (Hypsiboas pardalis and Physalaemus cuvieri) were observed in GLY toxicity tests, as indicated by the 96-h LC50 values (106 and 115 mg l−1 for P. cuvieri and H. pardalis, respectively) [280]. A lower concentration of the GBH Roundup Original (≥ 0.28 mg AI l−1) significantly increased DNA damage in D. minutus tadpoles [281]. Exposure to the GBH Glyphogan Classic (2 and 6.5 mg a.e. GLY l−1) caused behavioral changes in tadpoles of the agile frog Rana dalmatina [282]. At higher concentrations, reduced tadpole activity was observed with more tadpoles hiding. At the lower concentration tested, the vertical position of the tadpoles was closer to the water surface than in controls. In addition, some of the observed behavioral changes resembled the movements induced by the presence of predators, such as dragonfly larvae [282]. The effects of various GBHs (including Roundup Ultra-Max, Infosato, Glifoglex, and C-K Yuyos) on enzymatic parameters (such as reduced activity of AChE, carboxylesterase, GST, and butyrylcholinesterase), were demonstrated in tadpoles of Rhinella arenarum [283]. Tadpoles of B. bufo exposed to Glyphogan Classic GBH (4 mg a.e. GLY l−1) throughout larval development showed a higher amount of bufadienolides during metamorphosis compared to the control group [284]. Wood frog (L. sylvaticus) larvae exposed to the GBH Roundup WeatherMax (0.21 and 2.8 mg a.e. GLY l−1) had larger larvae, but no significant effects on larval development were observed [285]. Exposure to a Roundup Ultra-Max GBH (20 mg l−1) did not resulted in increased induction of DNA damage, oxidative stress or neurotoxicity. In addition, enzyme activities (e.g., butyrylcholinesteras, GST, and carboxylesterase activities) were not altered either. However, an increased heterophil l-1ymphocyte (H/L) ratio in peripheral blood was detected indicating immunological depression in R. arenarum [208].
Based on the results within an artificial pond mesocosm, the effects of the GBH GLY-4 Plus on survival, body size, and cellular immune response of spotted salamanders (Ambystoma maculatum) were strongly influenced by the applied UV-B light regimes (moderate or low) [286]. In larval salamanders (Eurycea wilderae) exposed to GBHs such as Roundup, shorter and more frequent movements were observed at higher GLY concentrations, while GLY-induced effects were inconsistently affected by water temperature [287].
Genotoxic, mutagenic, and histopathological hepatic effects of POEA and GLY were observed in lesser treefrog (D. minutus) tadpoles [288]. More genomic damage (174%) was observed in POEA-exposed tadpoles at all concentrations (1.25–10 μg l−1) compared to controls. Additionally, up to a sevenfold increase in micronuclei was recorded on average at 5 μg l−1 POEA. All individuals exposed to 10 μg l−1 POEA died. GLY exposure increased DNA damage by 165% at higher concentrations (260 and 520 μg l−1) and also gave rise to more micronuclei (up to sixfold) at 520 μg l−1 [288]. The mixture of the GBH Roundup Active and the surfactant Cosmo-Flux 411F caused concentration-dependent sublethal effects on the body size of tadpoles (e.g., Rhinella humboldti, Engystomops pustulosus, Hypsiboas crepitans) [289]. However, significant effects on embryonic development were observed only on R. humboldti. It was noted that embryos appeared to be significantly more tolerant compared to tadpoles, which may be explained by the exclusion of the chemical compounds of the embryonic membranes and the absence of surfactant-sensitive organs, such as the gills [289]. Alterations of swimming performance were not observed in the investigated microcosms [289]. Exposure to surfactant MON 0818 (POEA) resulted in 96-h LC50 values ranging from 0.68 to 1.32 mg l−1 in the North American anuran species (e.g., Rana pipiens, Rana clamitans, and Hyla chrysoscelis), indicating differences in the sensitivity of anuran species to this GBH co-formulant [290]. Most of the presented studies highlight that co-formulants are the main cause of high-level toxicity of pesticide formulations to amphibians. Similarly, in acute toxicity testing on R. dalmatina and B. bufo tadpoles, the mortality and body mass were not affected by GLY [283]. However, in the presence of the POEA, higher mortality was observed in both species with high toxicity of POEA alone was also demonstrated [291]. The results of the ecotoxicological studies on amphibians indicated several alterations in the physiological, morphological and metabolic parameters. Several effects were detected even at environmentally relevant GLY concentrations, demonstrating the particular vulnerability of amphibians (Table 9).
Combined effects between glyphosate and other environmental pollutants
The various chemical compounds (e.g., pesticide AIs, formulation agents, pharmaceutical residues) present in the different environmental matrices in all likelihood will come into contact with each other. GLY and its metabolites (e.g., AMPA) will coexist in the aquatic environments with the other aquatic pollutants. Therefore, identifying and evaluating the potential combined effects of these various pollutants is essential to conducting a comprehensive ERA for commercial pesticide formulations, including GBHs. The presented combined effects between GLY and other environmental pollutants are summarized in Tables 10 and 11.
Combined effects with other AIs, co-formulants, and other aquatic pollutants
The concern about ecotoxicological consequences and thus adverse effects of pesticide residues stem from possible additive or synergistic effects of combinations of various compounds of agricultural (and other) origin. Multi-and transgenerational synergistic effects of GLY and chlorpyrifos were observed in the estuarine rotifer P. similis exposed to the mixture of tested AIs at environmentally relevant concentrations [181]. Reduced growth was observed in generations F0 to F6, but the transgenerational effects were eliminated in F5, indicating a slight recovery and population resilience to pollution [181]. Simultaneous exposure of crayfish (Pontastacus leptodactylus) to the insecticide chlorpyrifos and GLY for 21 days resulted in synergic effects with an increase in glutamic-oxaloacetic-transaminase activity and total antioxidant content, while γ-glutamyltransferase (GGT) activity decreased whilst exposure to GLY alone increased GGT activity in P. leptodactylus [292]. The potential adverse effects of GLY (3.5 mg l−1) and chlorpyrifos (25 µg l−1) were assessed individually and in combination on common carp (C. carpio) over 21 days [293]. In addition to induced accumulation of malondialdehyde in the brain, decreased enzyme activities (e.g., AChE, catalase, GST) were observed after exposure to the test substances individually. In combination, the impact on most parameters measured were enhanced over that observed for the individual compounds suggesting that exposure to the investigated AIs both individually and in combination, may lead to oxidative stress and lipid peroxidation in common carp [293]. In addition, changes in the transcriptome were also detected in fish brains after treatment with GLY and chlorpyrifos in fish brains but again enhanced with the mixture of the two [293]. A synergistic effect of a mixture of the GBH Credit (50.0–100.0 mg l−1) and the dicamba-based commercial herbicide formulation Banvel (96.0–720.0 mg l−1) was demonstrated in the induction of primary DNA breaks in circulating blood cells of late-stage R. arenarum larvae [294]. Exposure to a higher concentration of the combined herbicides caused a significant increase in genetic damage index (GDI) [294]. Similarly, an increased GDI was observed with a combination of the Credit GBH and imazethapyr-based (Pivot) herbicides on R. arenarum tadpoles [295]. After co-exposure to the herbicides, synergistic effects were demonstrated in DNA damage induction based on measurements in blood cells compared to treatment with the single herbicide [295]. GLY and 2,4-D are the most commonly used herbicides worldwide with well over 700,000 and 150,000 tonnes applied per year, respectively [296], and are used singly and in combination for weed control in various crops such as cotton, soybean, and corn [297, 298]. Therefore, these two herbicide AIs are frequently detected in surface waters, especially near agricultural fields [35, 299,300,301,302,303]. The combination of GLY and 2,4-D had no effect on the survival of exposed Boana faber and L. latrans tadpoles although swimming activity and growth were significantly affected [303]. Additionally, various types of damage and abnormalities were observed in the intestine, mouth, and erythrocytes of tadpoles [303].
While the mechanism of how co-formulants enhance the uptake of pesticide AI is well known [17, 304], predicting negative impacts on the non-target organisms is not straightforward. Furthermore, conducting ecotoxicological testing on various co-formulants is difficult, as these components are usually not identified on the labels of commercial pesticide formulations with their exact composition often considered as confidential business information. Many studies have shown that co-formulants of GBH can affect toxicity, including phytotoxicity, cytotoxicity developmental neurotoxicity, genotoxicity, and endocrine-disrupting effects of GLY on various non-target organisms such as fish and amphibians [31, 32, 74, 175, 247, 277, 305, 306].
Other environmental pollutants, such as heavy metals, nanomaterials, and microplastics may be present in aquatic environments, and these chemical compounds may also interact with GLY residues and its metabolites. A concentration-dependent effect of a combination of copper and GLY on the growth and physiological response of Salvinia natans has been reported [307]. Antagonistic effects were observed in plants exposed to low concentrations of copper and GLY, while synergistic effects were observed at higher concentrations. Furthermore, higher levels of hydrogen peroxide malondialdehyde were detected after individual and combined exposure, indicating the occurrence of oxidative stress [307]. After exposure to a GBH (Faena, 1.04–1.57 mg l−1 GLY) and copper (2.45–4.31 µg l−1), a delayed age at first reproduction, an increased number of aborted eggs, reduced fecundity and a lower number of clutches per female were observed in the parental and F1 generations of Daphnia exilis [165]. In addition, reduced carbohydrate and lipid contents were detected in both generations [165]. The observed combined effects of GLY and copper were stronger in the F1 generation [165]. Due to the presence of arsenic in natural phosphate ores, their use in the production of agrochemicals and particularly phosphate fertilizers, may pose an additional risk to the environment and food safety [18, 308]. A worrying finding in this context is the detection of heavy metal (e.g., arsenic, chromium, nickel, lead) impurities and petroleum residues in 11 different GBHs (e.g., Glyphogan, Medallon Premium, Roundup Classic) [18]. The presence of impurities (e.g., heavy metal, residues of polycyclic aromatic hydrocarbons), may originate from the production phase of the commercial formulations and potentially can contribute to the toxicity of GBHs (e.g., possible endocrine disrupting effects, carcinogenicity, neurotoxicity) [18, 309, 310]. Therefore, regulators should require manufacturers to identify and quantify toxic impurities in commercial pesticide formulations.
In chronic tests, toxic multigenerational effects of a mixture of GLY and silver nanoparticles were observed in D. magna [173]. A significant delay in the release of the first offspring and altered reproductive parameters (reduced number of newborns) were also demonstrated in the unexposed and offspring exposed to the individual compounds. Simultaneous exposure to GLY and silver nanoparticles resulted in a higher degree of toxicity compared to that observed with the individual test substances. In acute toxicity testing, antagonistic and additive interactions were observed, possibly due to GLY forming complexes with the nanoparticles [173]. Simultaneous exposure of citrate-functionalized iron oxide nanoparticles and the GBH Roundup Original resulted in clastogenic (DNA damage) and aneugenic (cell nuclear alterations) time-dependent effects in guppies (P. reticulata) [311]. Synergistic effects were observed compared to controls and guppies exposed to nanoparticles alone [311]. In Nile tilapia (O. niloticus) exposed to a Roundup GBH (0.6 mg AI l−1), the toxic effects of GLY, such as induction of oxidative stress and immunosuppression were alleviated in the presence of propolis nanoparticles fed to exposed animals compared to the GLY-alone exposed group. This was evident through reduced gill and liver glutathione concentrations and decreased white and red blood cell counts [312]. Circulatory damages, inflammatory responses, and the activation of the immune system were observed in P. reticulata exposed to the mixture of a GBH (Roundup Original) and iron oxide nanoparticles [313]. Additionally, concentration-dependent ultrastructural alterations were observed [313].
In the environment, plastic waste can undergo degradation processes that lead to the formation of micro- and nano-plastics. These micro- and nano-plastics can directly and indirectly affect aquatic organisms, and can adsorb other chemical compounds, leading to combined contamination. The antagonistic combined toxicity of GLY and polystyrene nanoparticles modified with cationic amino acids, was observed in the inhibition of the growth of blue-green algae (M. aeruginosa) [314]. This was attributed to the high adsorption capacity of nanoparticles for GLY, resulting in a lower inhibitory effect of this herbicide AI. The presence of GLY increased the stability of the dispersion system, allowing for higher adsorption of nanoparticles on the surface of algal cells, which may lead to biomagnification of nanoparticles in food webs [314]. Synergistic effects were demonstrated in D. magna exposed to a combination of GLY and polystyrene nano-plastic [315]. Simultaneous exposure of the tested compounds resulted in increased immobility and production of ROS, while swimming activity decreased. Multigenerational responses were also observed after exposure of the parental (F0) generation of daphnids to the mixture of GLY and nano-plastic, with altered reproductive parameters in the F1 and F2 generations as indicated in recovery tests [315]. The tested GLY forms (GLY acid, GLY-IPA, and GBH Roundup Gran) also increased the mortality of D. magna in the presence of microplastics such as polyethylene microbeads and polyethylene terephthalate/polyamide fibers, while the interaction between the treatment and time was not significant [316]. After 60 days of exposure to a combination of GLY (15 mg l−1) and polyethylene microplastics (4.5 mg l−1), free-swimming behavior of C. carpio was found to be inhibited [252]. Microplastics alone and in combination with GLY disturbed physical and chemical intestinal barriers in exposed fish. Altered abundance and diversity of the gut microbiota and changes in amino acid and lipid metabolism were also observed with simultaneous exposure to the test compounds [252].
Combined effects with pathogens and parasites
Exposure to a low concentration (1 μg l−1) of GLY and GBHs (Roundup Innovert and Viaglif Jardin) had an impact on the susceptibility of rainbow trout O. mykiss fish to viral infection, specifically to hematopoietic necrosis virus [317]. Roundup Innovert significantly reduced cumulative mortality, while exposure to Viaglif Jardin resulted in increased mortality of O. mykiss, whereas pure GLY had little effect on the endpoints studied [317]. Furthermore, exposure to a higher concentration (500 μg l−1) of GLY or its GBH formulations caused significant differences in red and white blood cell counts and altered enzymatic activities in O. mykiss infected with infectious hematopoietic necrosis virus after a 96-h exposure and 96-h post-viral infection [318].
Individual exposure to a GBH (0.36 mg AI l−1) and the trematode parasite Telogaster opisthorchis, did not affect the survival of juvenile roundhead galaxias (Galaxias anomalus) fish [319]. However, simultaneous exposure to GLY and parasitic T. opisthorchis infection significantly decreased fish survival. Juvenile fish exhibited spinal malformations after exposure to the infection alone and in combination with GLY, and synergistic effects were observed between GLY and the presence of parasites. GLY at a moderate concentration (3.6 mg AI l−1) resulted in significantly higher production of T. opisthorchis cercariae in their snail intermediate host, the New Zealand mud snail (Potamopyrgus antipodarum), compared to the control group [319]. In the fish L. rohita, a significantly increased susceptibility to the pathogen Aeromonas hydrophila was observed in the presence of a GBH at sub-lethal concentrations (Roundup, 0.63–13.6 mg AI l−1) [222]. Therefore, reduced survivability and increased susceptibility to the infection was observed in GBH exposed fish [222].
The detected interactions between GLY/GBH and other environmental pollutants are immensely complex effects. The presented combined effects between GLY and pathogens or parasites are summarized in Table 11. The combined toxicity of various chemical compounds is understudied, whilst during the ERA regulatory agencies generally rely on results obtained solely from standard laboratory studies using test organisms exposed to a range of concentrations of single compounds. However, under natural conditions, organisms come into contact with a very wide range of environmental pollutants. From the studies presented here, it appears that numerous aquatic pollutants can alter the effects of GLY and GBHs.
Comparison with the 2023 EFSA conclusion on aquatic toxicity of GLY/GBH
The most recent conclusion on the peer review of the risk assessment of GLY was published by EFSA on 26 July 2023 [320]. The document provides an evaluation of the risk profile of GLY based on undisclosed studies submitted by the manufacturers and the publicly available peer-reviewed scientific literature. According to the conclusions, the overall data provided in the risk assessment of GLY were considered sufficient for the assessment of environmental exposure, but concerns were raised about the potential exposure of groundwater via infiltration or contaminated surface water bodies due to the large proportion of land treated with GLY. This was recognized as a data gap. Furthermore, the surface water monitoring for GLY and AMPA residues carried out by the applicants, showed weaknesses in methodology and the use of minimum quality criteria and was, therefore, considered to have limited suitability for regulatory purposes. These issues are critical as they may impact the ecological health and the safety of water sources. Overall, the EFSA conclusion highlights general data gaps and potential risks and refers to the lack of harmonized methods and sufficient data on the adverse effects on aquatic macrophytes, broader ecological impacts, or the aquatic stage of amphibians. In addition to these uncertainties, the assessment does not conclude on certain areas such as adverse effects on biofilms or changes in microbial communities.
Therefore, our review aquatic ecotoxicology on different groups of aquatic organisms (from microbial communities, cellular and high-ordered macrophytes to aquatic invertebrates and vertebrates) is an essential complement to adequately assess the impact of increased use of GLY/GBHs [320]. Based on EFSAs conclusion and the results of the reported ecotoxicological studies, it is essential to develop state of the art guidelines to adequately address all environmental hazards from the use of GLY/GBHs, including the most sensitive species. According to the EU Pesticide Law (Regulation (EC) 1107/2009), the same level of safety should be ensured for a pesticide product as for the AI. Pesticide exposure under real environmental conditions occurs in the form of commercial pesticide formulations, but is only taken into account in the EU in a second stage at the Member State level. To comply with EU legislation and protect human health and the environment, studies on AIs and formulations should be considered during the risk assessment for the authorization of AIs.
In addition, stricter regulation of co-formulants per se is needed, as a co-formulant can affect the toxicity of the formulation and the fate of the AI in the environment. However, Annex III of Regulation (EC) 1107/2009, which is supposed to contain the list of banned co-formulants in commercial pesticide formulations, still does not contain an entry [36]. This is difficult to understand from a scientific point of view, as there is ample evidence for the acute and chronic toxicity of this class of substances. Moreover, a standardized approach should be developed to assess the combined toxicity of different co-occurring chemical compounds. The ecotoxicological assessment of the individual co-formulants and the combined effects of the components contained in formulated products should be an essential part of a comprehensive ERA for commercial pesticide formulations.
Civil society has criticized the EFSA conclusion referring to the cancerogenic and neurotoxicological potential of GLY [320] and the scientific information and data gaps identified, including the lack of information on the long-term toxicity of one of the representative uses that should have been identified as critical areas of concern by EFSA. However, EFSA’s definition of critical areas of concern is clear: if it is established that no safe use can be ensured, if the risk assessment cannot be finalized, or if the criteria laid down in Article 4 of Regulation (EC) 1107/2009 are not met, the EFSA must establish a critical area of concern for one or several endpoints [36]. The state-of-the-art of independent science proves that the harm caused by GLY and its formulations is unacceptable, which was not made clear in the ECHA and EFSA assessment [321]. EFSAs recent conclusions on GLY recognizes that GLY is toxic to aquatic organisms (category chronic 1—toxic ≤ 0.1 mg l−1, category chronic 2—toxic between 0.1 and 1 mg l−1). In addition, data gaps on aquatic toxicity to aquatic macrophytes and open questions regarding the impact on biodiversity through indirect effects and trophic interactions were identified. These data gaps, the independent studies on the impact of GLY and AMPA on aquatic life, and our findings regarding the current levels of GLY and AMPA contamination of surface waters indicate that the approval criteria are not met.
Despite identified adverse effects of GLY in the scientific literature and the data gaps identified in the EFSA conclusion, the European Commission proposed to re-authorize GLY with certain restrictions. On 28 November 2023, the Commission implementing (EU) Regulation 2023/2660 was published, with allows GLY in the EU for 10 years, with several binding and non-binding restrictions [322]. These include a ban on desiccation with GBH and the requirement to Member States to pay particular attention to the following: (i) uses by non-professional users, (ii) residues that may be present in succeeding crops grown in rotations, (iii) the protection of groundwater in vulnerable areas and of surface waters, (iv) the protection of small herbivorous mammals, (v) the protection of non-target terrestrial and aquatic plants from exposure by spray drift, and (vi) indirect effects on biodiversity via trophic interactions once relevant methods and guidance to identify such effects are agreed at Union level. In addition to this last requirement, the Commission requested that the applicant (companies that applied for the reauthorization of GLY) to submit within three years confirmatory information on the possible indirect effects on biodiversity through trophic interactions. The Commission also proposed maximum application rates, which may only be exceeded if appropriate risk assessments are available. As several national authorities, particularly in smaller Member States, do not have sufficient capacity and resources, it is unlikely that the above listed provisions will be fulfilled. In addition, the status of GLY in the EU, characterized by the recent renewal with additional restrictions, contrasts with the situation in other countries, where there is a complete ban in some countries, cautious use in others, and ongoing legal and public debates that continue to influence policy and perceptions of this widely used herbicide.
Our review is not based on the manufacturers’ studies. Some of the studies presented in our review are not included in the EFSA conclusion [320], which has been subject to criticisms, as they indicate the potential harm that GLY/GBHs can cause to aquatic species and ecosystems. Hence, the present review clearly complements EFSAs conclusion and provides novel views. Furthermore, the EFSA conclusion is not really user-friendly as the references are fragmented and lack a single, complete and clear reference section. In addition, the names of authors and publications are often blacked out and not searchable. This review also contains studies that were not included in the EFSA conclusion because they were not considered compliant with Good Laboratory Practice (GLP).
Conclusions
It is widely assumed, especially within regulatory agency circles, that the effects of GLY and its commercial formulations are specific and affect only the target plant species. However, the extensive evidence presented in this review demonstrates that GLY/GBHs can have multiple effects on non-target organisms in aquatic ecosystems. Due to the physiochemical properties of GLY, it can easily enter the aquatic environment. Similarly, multiple effects of GLY and GBHs on terrestrial ecosystems has also evidently been shown [323]. The risks associated with the ecotoxicity of GLY and associated co-formulants in GBHs most likely arise from the higher residue levels resulting from consistent and frequent large-scale application. In general, commercial pesticide formulations consist of AIs and various co-formulants to enhance effectiveness, which includes improving the bioavailability of AIs. These co-formulants have been considered as inactive components with respect to the intended biological effect of commercial pesticide formulations. However, a large and growing number of scientific studies have unequivocally demonstrated the high toxicity of the co-formulants in their own right [31, 32]. This increased combined toxicity of the components present in commercial pesticide formulations has been demonstrated for POEA and many other co-formulants in GBHs [31, 32]. Consequently, POEA has been banned in GBHs under current EU legislation although POEA replacements (e.g., Dodigen 4022, propoxylated quaternary ammonium surfactant) purported as safe alternatives have also proven to be toxic [33, 324]. Therefore, co-formulants cannot be considered inert or inactive ingredients.
The occurrence of residues of GBHs in surface waters is now a globally observed phenomenon. There is a substantial quantity of scientific data available on the acute toxicity of GLY. However, it is difficult to extrapolate and compare the results because the sensitivity of the test organisms, the test conditions, and the composition of the GBHs vary, even if they have the same trade name. Although GLY may be less acutely toxic compared to other herbicidal AIs, unintended adverse outcomes from GLY exposure have been demonstrated in numerous studies on a wide range of aquatic organisms, including aquatic microorganisms, zooplankton, mollusks, and higher order aquatic plants, fish and amphibians.
One of the fundamental mechanisms underlying these negative effects on the health of various organisms is the induction of oxidative stress, and metabolic and endocrine disruption, which in some cases results in DNA damage [106, 107, 117, 203, 214, 215, 281, 288, 325]. These effects lead to various changes in physiological processes. According to the results of research studies, the tested behavioral endpoints should also be considered during the ERA of pesticides including GBHs. Behavior, as a sublethal endpoint measurement, provides a particularly sensitive and early indication of biotic disruptions and damage compared to severe physiological and mortality-based endpoints [326,327,328,329]. The exceptionally high use of GLY has exceeded 800 thousand tons per year since 2014 [39], with current estimates suggesting that it has now exceeded one megaton per year worldwide. Even at a conservative estimate, this amount of GLY is equivalent to three times the amount of phosphorus fertilizer applied annually, in terms of phosphorus content. If GLY is washed into standing water bodies, it can therefore significantly contribute to eutrophication. Currently GLY is the leading pesticide in the market and its use is projected to increase 4.5-fold between 2022 and 2029. This extremely high rate of usage poses a substantial environmental burden resulting in increased exposure and risks to non-target organisms.
Another important issue to address is the consequences of evaluated levels of AMPA, the primary GLY degradation product, in relation to GLY residues found in various water matrices, including surface and drinking water. However, it should be noted that AMPA can be formed not only by the degradation of GLY, but also by its use as a water softener. In the EU, AMPA is not considered a significant metabolite to be taken into account when evaluating the parametric values for GLY in drinking water (0.1 ng ml−1) established in the European Drinking Water Directive (EU) 2020/2184 for pesticide active substances and their relevant metabolites. Nevertheless, some nations such as Denmark, Hungary and France apply a limit value of 0.1 μg l−1 for AMPA in drinking water as is the case for pesticide AIs. There is currently no environmental quality standard (EQS) for either GLY or AMPA at the EU level. In a recent proposal, the European Commission revised the list of priority substances for surface water and included an extremely high EQS value for GLY, which would allow a higher level of contamination compared to drinking water safety standards. The same proposal included a threshold of 0.5 µg l−1 (AA-EQS—annual average of environmental quality standard) for the combined concentration of pesticide AIs or relevant metabolites, and degradation and reaction products. At the time of writing of this review, the European Commission and EU Member States have not yet determined whether metabolites such as AMPA, which evidently pose a risk to the aquatic environment, will be included in this threshold limit, nor have final EQS values been set by EU policy makers. In 2023, the European Parliament voted on a more ambitious AA-EQS of 0.1 µg l−1 for inland surface waters, which is under discussion in the European Council.
Numerous studies assessed in this review indicated that AMPA can have equal and sometimes even stronger detrimental effects compared to GLY in given life stages of aquatic organisms including microorganisms [101], algae and aquatic plants [148, 154], echinoderms and mollusks [196, 199, 201, 330] and fish [234, 246, 255, 258]. AMPA is more persistent in the environment, and EFSAs conclusion of 2023 state that the toxicological profile of AMPA is similar to the toxicity of GLY [320, 331]. Therefore, both AMPA and GLY concentrations should be considered when setting the limit for drinking water. In this regard, the fact that AMPA as a residue may originate from other industrial uses rather than the metabolism of GLY is ecotoxicologically irrelevant. Both GLY and AMPA pose a risk to the aquatic environment, and GLY is already classified as being toxic to aquatic life with long-lasting effects (Aquatic Chronic 2; H411). However, certain studies [81, 84] would justify a more stringent classification.
The combination of GLY and co-formulants often leads to additive or synergistic effects. Furthermore, GLY, GBHs, and even the co-formulants can induce a wide range of lethal or sublethal ecotoxicological outcomes as demonstrated in numerous non-target aquatic organisms even at very low concentrations of exposure (Fig. 1) [198, 201, 216]. Aquatic organisms are highly exposed to aquatic pollutants, and their direct contact with these xenobiotics in water is unavoidable. Therefore, routine monitoring of their exposure is necessary, and the current aquatic toxicity classification of GLY and GBHs should be re-evaluated. The toxicity of GLY in the aquatic environment varies significantly among different species in all taxa and is influenced by exposure conditions such as timing, duration, and extent [74]. Recently, the toxic effects of GLY on amphibians have gained attention in research, indicating that amphibians are particularly susceptible to the effects of GBHs compared to other vertebrates due to their specific lifestyle, which includes both aquatic and terrestrial environments during different life stages [273].
This review presents the results of scientific research that examines the aquatic ecotoxicity of GLY and its commercial formulations as well as the co-formulants present in GBHs. Our review is not based on studies conducted by the manufacturers. Some of the presented results are not included in the EFSA conclusion published in July 2023 [320]. The observed adverse effects have been demonstrated using a wide variety of endpoints, methods and thresholds to assess the exposure and potential outcomes of the tested substances. It can be concluded that we do not fully know the exact unintended effects of GLY on aquatic non-target organisms and ecosystems even after several decades of GBH use. One of the main problems hindering ecotoxicological assessment is the lack of knowledge of the exact composition of GBHs, which is withheld on the grounds of confidential business information and, therefore, not published. There is still a great need for studies to evaluate the potential toxic effects of co-formulants in GBHs. The current regulation is based on an ERA performed on the AI or commercial pesticide formulations used only once or a few times on a given crop. This is despite the fact that in standard agricultural practice multiple applications of commercial pesticide formulations are conducted during a cultivation cycle. In addition, the effects of commercial pesticide formulations are evaluated on each group of test organisms separately during ERA with interactions between the different trophic levels of the ecosystem not included in the assessment [332, 333]. Furthermore, ERA does not prescribe in-field risks, although biodiversity conservation must be supported to ensure important ecosystem services [333]. The consequences of decades of multiple uses GBHs are not assessed.
In summary, this review has identified important knowledge gaps for a systematic and comprehensive assessment of the aquatic ecotoxicity of GLY and GBH. Therefore, we recommend that the current ERAs be updated to include the following non-exhaustive list of issues:
-
Supplement the predominantly short-term, single-species aquatic toxicity testing of GLY and GBH with a focus on aquatic primary producers, invertebrates, or vertebrate (such as fish and amphibians) with multispecies and trophic interactions and indirect effects on aquatic food webs and surrounding landscape.
-
At a minimum, include amphibians and reptiles in ERA species lists, as they are among the most threatened species on Earth.
-
Investigate the contribution of all ingredients of a GBH, including the various GLY AIs, co-formulants, and other contaminants such as heavy metals [18].
-
Evaluate effects on the composition and function of aquatic microbiota inhibited by GLY-effects on their shikimate metabolic pathway.
-
Conduct systematic long-term monitoring studies on the effects of high and low chronic exposure in aquatic species with different generation times.
-
Evaluate interactions with other contaminants in freshwater and marine ecosystems such as agrochemicals, antibiotics, other chemicals, nutrients, microplastics, light pollution, parasites and climate change factors.
-
Explore the impacts of GLY and GBHs on aquatic biodiversity, the consequences of biofilms on food quality at higher trophic levels, and other indirect bottom-up and top-down effects [333].
Some of these knowledge gaps are similar to those previously noted in our review on terrestrial ecotoxicity of GLY and GBHs [323] and also highlighted in the last EFSA Conclusion [320]. Apparently, government regulatory agencies have neglected the ecologically relevant extent of aquatic ecotoxicity in the ERA of GLY and GBHs for decades. Given the serious non-target effects on aquatic ecosystems already identified, and before these serious knowledge gaps are adequately addressed in the ERAs, the precautionary principle enshrined in EU law would actually recommend that GLY/GBHs be withdrawn from the EU market. The current environmental risk assessments and regulatory measures for GLY/GBHs are clearly inadequate to protect aquatic ecosystems and biodiversity.
GBHs mentioned in this review
Aria; Biocarb; C-K Yuyos; Clinic; Credit; Enviro; Factor 540R; Faena; Forceup; Glifoglex; Glifosato II Atanor; GLY-4 Plus; Glyphogan; Glyphogan Classic; Infosato; Kilo Max; Medallon Premium; Orium; Roundup; Roundup Active; Roundup Allées et Terrasses; Roundup Classic; Roundup Express; Roundup Flex; Roundup Full II; Roundup Gran; Roundup Innovert; Roundup LB Plus; Roundup Max; Roundup Power 2.0; Roundup PowerFlex; Roundup Original; Roundup Original MAX; Roundup Original DI; Roundup SL; Roundup Star; Roundup Transorb; Roundup Ultra 360 SL; Roundup UltraMax; Roundup WeatherMax; Roundup Weed & Grass Killer; Sulfosato Touchdown; Sumin Atut; Taifun Forte; Viaglif Jardin; VisionMax.
Availability of data and materials
All data generated or analyzed during this study are included in this published article.
Abbreviations
- AA-EQS:
-
Annual average of environmental quality standard
- AChE:
-
Acetylcholinesterase
- a.e.:
-
Acid equivalent
- AI:
-
Active ingredient
- AMPA:
-
Aminomethylphosphonic acid
- APG:
-
Alkyl polyglucoside
- chl-a:
-
Chlorophyll-a
- DNA:
-
Deoxyribonucleic acid
- EC50 :
-
50% Effective concentration
- ECHA:
-
European Chemical Agency
- EFSA:
-
European Food Safety Authority
- EPS:
-
Extracellular polymeric substances
- EQS:
-
Environmental quality standard
- ERA:
-
Environmental risk assessment
- EU:
-
European Union
- GBH:
-
Glyphosate-based herbicide
- GDI:
-
Genetic damage index
- GGT:
-
γ-Glutamyltransferase
- GLY:
-
Glyphosate
- GLY-IPA:
-
Glyphosate-isopropylammonium salt
- GST:
-
Glutathione-S-transferase
- GT:
-
Glyphosate-tolerant
- GM:
-
Genetically modified
- IC50 :
-
50% Inhibitory concentration
- LC50 :
-
50% Lethal concentration
- ppm:
-
Parts per million
- MXR:
-
Multixenobiotic resistance
- POEA:
-
A mixture of polyethoxylated tallow amines
- ROS:
-
Reactive oxygen species
- RTG-2:
-
Rainbow trout gonad-2
- SOD:
-
Superoxide dismutase
- TBARS:
-
Thiobarbituric acid reactive species
References
Székács A, Darvas B (2012) Forty years with glyphosate. In: Hasaneen MN (ed) Herbicides—properties, synthesis and control of weeds. InTech, Rijeka, pp 247–284. https://doi.org/10.5772/32491
Casida JE (2017) Organophosphorus xenobiotic toxicology. Annu Rev Pharmacol Toxicol 57:309–327. https://doi.org/10.1146/annurev-pharmtox-010716-104926
Mesnage R, Szekács A, Zaller JG (2021) Herbicides: Brief history, agricultural use, and potential alternatives for weed control. In: Mesnage R, Zaller J (eds) Herbicides: chemistry, efficacy, toxicology, and environmental impacts. Emerging issues in analytical chemistry. Elsevier, Amsterdam, pp 1–20. https://doi.org/10.1016/B978-0-12-823674-1.00002-X
Dill GM, Sammons RD, Feng PCC, Kohn F, Kretzmer K, Mehrsheikh A, Bleeke M, Honegger JL, Farmer D, Wright D, Haupfear EA (2010) Glyphosate: Discovery, development, applications, and properties. In: Nandula VK (ed) Glyphosate resistance in crops and weeds. John Wiley & Sons Inc., Hoboken, pp 1–33. https://doi.org/10.1002/9780470634394.ch1
Swanson N, Leu A, Abrahamson J, Wallet B (2014) Genetically engineered crops, glyphosate and the deterioration of health in the United States of America. J Org Syst 9:6–37
Benbrook CM (2016) Trends in glyphosate herbicide use in the United States and globally. Environ Sci Eur 28:3. https://doi.org/10.1186/s12302-016-0070-0
Martins-Gomes C, Silva TL, Andreani T, Silva AM (2022) Glyphosate vs. glyphosate-based herbicides exposure: a review on their toxicity. J Xenobiot 12:21–40. https://doi.org/10.3390/jox12010003
Benbrook CM, Benbrook R (2021) A minimum data set for tracking changes in pesticide use. In: Mesnage R, Zaller J (eds) Herbicides: chemistry, efficacy, toxicology, and environmental impacts. Emerging issues in analytical chemistry. Elsevier, Amsterdam, pp 21–40
Antier C, Kudsk P, Reboud X, Ulber L, Baret PV, Messéan A (2020) Glyphosate use in the European agricultural sector and a framework for its further monitoring. Sustainability 12:5682. https://doi.org/10.3390/su12145682
ReportLinker (2021) Global glyphosate market to reach $8.9 billion by 2026. GlobeNewswire, Los Angeles, USA. https://www.globenewswire.com/news-release/2021/10/18/2315706/0/en/Global-Glyphosate-Market-to-Reach-8-9-Billion-by-2026.html. Accessed 14 Jan 2024
PAN (2023) Weed management: alternatives to the glyphosate use. Pesticide Action Network Europe, Belgium, https://www.pan-europe.info/resources/reports/2023/03/weed-management-alternatives-use-glyphosate. Accessed 14 Jan 2024
Herrmann KM, Weaver LM (1999) The shikimate pathway. Ann Rev Plant Physiol Plant Mol Biol 50:473–503. https://doi.org/10.1146/annurev.arplant.50.1.473
Boocock MR, Coggins JR (1983) Kinetics of 5-enolpyruvylshikimate-3-phosphate synthase inhibition by glyphosate. FEBS Lett 154:127–133. https://doi.org/10.1016/0014-5793(83)80888-6
Tohge T, Watanabe M, Hoefgen R, Fernie A (2013) Shikimate and phenylalanine biosynthesis in the green lineage. Front Plant Sci. https://doi.org/10.3389/fpls.2013.00062
Defarge N, Takács E, Lozano VL, Mesnage R, Vendômois JS, Seralini GE, Székács A (2016) Co-formulants in glyphosate-based herbicides disrupt aromatase activity in human cells below toxic levels. Int J Environ Res Pub Health 13:264. https://doi.org/10.3390/ijerph13030264
Travlos I, Cheimona N, Bilalis D (2017) Glyphosate efficacy of different salt formulations and adjuvant additives on various weeds. Agronomy 7:60. https://doi.org/10.3390/agronomy7030060
Foy C (1987) Adjuvants: terminology, classification, and mode of action. In: Chow P, Grant C, Hinshalwood A, Simundson E (eds) Adjuvants and agrochemicals. CRC Press, Boca Raton, pp 1–15. https://doi.org/10.1201/9781351069489
Defarge N, Spiroux de Vendômois J, Séralini GE (2018) Toxicity of formulants and heavy metals in glyphosate-based herbicides and other pesticides. Toxicol Rep 5:156–163. https://doi.org/10.1016/j.toxrep.2017.12.025
Defarge N, Otto M, Hilbeck A (2023) A roundup herbicide causes high mortality and impairs development of Chrysoperla carnea (Stephens) (Neuroptera: Chrysopidae). Sci Tot Environ 865:161158. https://doi.org/10.1016/j.scitotenv.2022.161158
Evans SC, Shaw EM, Rypstra AL (2010) Exposure to a glyphosate-based herbicide affects agrobiont predatory arthropod behaviour and long-term survival. Ecotoxicol 19:1249–1257. https://doi.org/10.1007/s10646-010-0509-9
Tahir HM, Basheer T, Ali S, Yaqoob R, Naseem S, Khan SY (2019) Effect of pesticides on biological control potential of Neoscona theisi (Araneae: Araneidae). J Insect Sci 19:17. https://doi.org/10.1093/jisesa/iez024
Niedobova J, Skalsky M, Ouředničkova J, Michalko R, Bartoškova A (2019) Synergistic effects of glyphosate formulation herbicide and tankmixing adjuvants on Pardosa spiders. Env Poll 249:338–344. https://doi.org/10.1016/j.envpol.2019.03.031
Baglan H, Lazzari CR, Guerrieri FJ (2018) Glyphosate impairs learning in Aedes aegypti mosquito larvae at field-realistic doses. J Exp Biol 221:jeb187518. https://doi.org/10.1242/jeb.187518
Graffigna S, Marrero HJ, Torretta JP (2021) Glyphosate commercial formulation negatively affects the reproductive success of solitary wild bees in a Pampean agroecosystem. Apidologie 52:272–281. https://doi.org/10.1007/s13592-020-00816-8
Balbuena MS, Tison L, Hahn M-L, Greggers U, Menzel R, Farina WM (2015) Effects of sublethal doses of glyphosate on honeybee navigation. J Exp Biol 218:2799–2805. https://doi.org/10.1242/jeb.117291
Zgurzynski MI, Lushington GH (2019) Glyphosate impact on Apis mellifera navigation: a combined behavioral and cheminformatics study. Pharmacol Toxicol 7:806–824
Fishel F (2020) What are inert ingredients? Pesticide Information Office, Gainesville, USA, https://edis.ifas.ufl.edu/publication/PI081. Accessed 14 Jan 2024
US EPA (2022) Use of term “Inert” in the label ingredients statement. Pesticide Registration (PR) Notice 97–6. Office of Prevention, Pesticides and Toxic Substances, Office of Pesticide Programs, U.S. Government Printing Office, Washington DC, USA, https://www.epa.gov/pesticide-registration/prn-97-6-use-term-inert-label-ingredients-statement. Accessed 14 Jan 2024
Mesnage R (2021) Coformulants in commercial herbicides. In: Mesnage R, Zaller J (eds) Herbicides: chemistry, efficacy, toxicology, and environmental impacts. Emerging issues in analytical chemistry. Elsevier, Amsterdam, pp 87–112
Tsui MTK, Chu LM (2003) Aquatic toxicity of glyphosate-based formulations: comparison between different organisms and the effects of environmental factors. Chemosphere 52:1189–1197. https://doi.org/10.1016/S0045-6535(03)00306-0
Székács A (2017) Mechanism-related teratogenic, hormone modulant and other toxicological effects of veterinary and agricultural surfactants. Insights Vet Sci 1:24–31. https://doi.org/10.29328/journal.ivs.1001003
Mesnage R, Benbrook C, Antoniou MN (2019) Insight into the confusion over surfactant co-formulants in glyphosate-based herbicides. Food Chem Toxicol 128:137–145. https://doi.org/10.1016/j.fct.2019.03.053
Mesnage R, Mandrioli D, Falcioni L, Belpoggi F, Brandsma I, Bourne B, Savage E, Mein CA, Antoniou MN (2022) Comparative toxicogenomics of glyphosate and Roundup herbicides by mammalian stem cell-based genotoxicity assays and molecular profiling in Sprague-Dawley rats. Toxicol Sci 186:83–101. https://doi.org/10.1093/toxsci/kfab143
Schmidt R, Spangl B, Edith Gruber E, Takács E, Mörtl M, Sz K, Székács A, Zaller JG (2023) Glyphosate effects on earthworms: active ingredients vs. commercial herbicides at different temperature and soil organic matter levels. Agrochem 2:1–16. https://doi.org/10.3390/agrochemicals2010001
European Commission (2016) Commission Implementing Regulation (EU) 2016/1313 of 1 August 2016 amending Implementation Regulation (EU) No 540/2011 as regards the conditions of approval of the active substance glyphosate. OJ EU L208:1–3. https://eur-lex.europa.eu/legal-content/EN/TXT/?uri=uriserv%3AOJ.L_.2016.208.01.0001.01.ENG. Accessed 14 Jan 2024
European Parliament and Council (2009) Regulation (EC) No 1107/2009 of the European Parliament and of the Council of 21 October 2009 concerning the placing of plant protection products on the market and repealing Council Directives 79/117/EEC and 91/414/EEC. OJ EU L309:1–50. https://eur-lex.europa.eu/LexUriServ/LexUriServ.do?uri=OJ:L:2009:309:0001:0050:en:PDF. Accessed 14 Jan 2024
Klátyik Sz, Bohus P, Darvas B, Székács A (2017) Authorization and toxicity of veterinary drugs and plant protection products: residues of the active ingredients in food and feed and toxicity problems related to adjuvants. Front Vet Sci 4:146. https://doi.org/10.3389/fvets.2017.00146
Panizzi S, Suciu NA, Trevisan M (2017) Combined ecotoxicological risk assessment in the frame of European authorization of pesticides. Sci Tot Environ 580:136–146. https://doi.org/10.1016/j.scitotenv.2016.10.154
Székács A, Darvas B (2018) Re-registration challenges of glyphosate in the European Union. Front Environ Sci 6:78. https://doi.org/10.3389/fenvs.2018.00078
Gower SA, Loux MM, Cardina J, Harrison SK (2002) Effect of planting date, residual herbicide, and postemergence application timing on weed control and grain yield in glyphosate-tolerant corn (Zea mays). Weed Technol 16:488–494. https://doi.org/10.1614/0890-037X(2002)016[0488:EOPDRH]2.0.CO;2
Whigham DK, Stoller EW (1979) Soybean desiccation by paraquat, glyphosate, and ametryn to accelerate harvest. Agron J 71:630–633. https://doi.org/10.2134/agronj1979.00021962007100040027x
Székács A, Mörtl M, Darvas B (2015) Monitoring pesticide residues in surface and ground water in Hungary: surveys in 1990–2015. J Chem 2015:717948. https://doi.org/10.1155/2015/717948
Borggaard OK, Gimsing AL (2008) Fate of glyphosate in soil and the possibility of leaching to ground and surface waters: a review. Pest Manag Sci 64:441–456. https://doi.org/10.1002/ps.1512
Hébert M-P, Fugère V, Gonzalez A (2019) The overlooked impact of rising glyphosate use on phosphorus loading in agricultural watersheds. Front Ecol Environ 17:48–56. https://doi.org/10.1002/fee.1985
Zaller JG, Weber M, Maderthaner M, Gruber E, Takács E, Mörtl M, Klátyik Sz, Győri J, Römbke J, Leisch F, Spangl B, Székács A (2021) Effects of glyphosate-based herbicides and their active ingredients on earthworms, water infiltration and glyphosate leaching are influenced by soil properties. Environ Sci Eur 33:51. https://doi.org/10.1186/s12302-021-00492-0
Kjær J, Olsen P, Ullum M, Grant R (2005) Leaching of glyphosate and amino-methylphosphonic acid from Danish agricultural field sites. J Environ Qual 34:608–620. https://doi.org/10.2134/jeq2005.0608
Tush D, Meyer MT (2016) Polyoxyethylene tallow amine, a glyphosate formulation adjuvant: Soil adsorption characteristics, degradation profile, and occurrence on selected soils from agricultural fields in Iowa, Illinois, Indiana, Kansas, Mississippi, and Missouri. Environ Sci Technol 50:5781–5789. https://doi.org/10.1021/acs.est.6b00965
U.S. Department of Agriculture - Economic Research Service (2023) Adoption of genetically engineered crops in the U.S. https://www.ers.usda.gov/data-products/adoption-of-genetically-engineered-crops-in-the-u-s/. Accessed 14 Jan 2024
Tush D, Maksimowicz MM, Meyer MT (2018) Dissipation of polyoxyethylene tallow amine (POEA) and glyphosate in an agricultural field and their co-occurrence on streambed sediments. Sci Total Environ 636:212–219. https://doi.org/10.1016/j.scitotenv.2018.04.246
Morrás H, Behrends Kraemer F, Sainz D, Fernández P, Chagas C (2022) Soil structure and glyphosate fate under no-till management in the Pampa region. II. Glyphosate and AMPA persistence and spatial distribution in the long-term. A conceptual model. Soil Tillage Res 223:105471. https://doi.org/10.1016/j.still.2022.105471
U.S. Geological Survey (2014) Common weed killer is widespread in the environment, U.S. Geological Survey, Reston, USA, https://www.usgs.gov/programs/environmental-health-program/science/common-weed-killer-widespread-environment. Accessed 14 Jan 2024
Caprile AC, Aparicio V, Sasal C, Andriulo E (2017) Variation in glyphosate and AMPA concentrations of surface water and groundwater. Geophys Res Abstr 19, EGU2017-2068. https://meetingorganizer.copernicus.org/EGU2017/EGU2017-2068.pdf. Accessed 14 Jan 2024
EFSA (2013) Guidance on tiered risk assessment for plant protection products for aquatic organisms in edge-of-field surface waters. EFSA J 11:3290. https://doi.org/10.2903/j.efsa.2013.3290
Coupe RH, Kalkhoff SJ, Capel PD, Gregoire C (2012) Fate and transport of glyphosate and aminomethylphosphonic acid in surface waters of agricultural basins. Pest Manag Sci 68:16–30. https://doi.org/10.1002/ps.2212
Mörtl M, Németh G, Juracsek J, Darvas B, Kamp L, Rubio F, Székács A (2013) Determination of glyphosate residues in Hungarian water samples by immunoassay. Microchem J 107:143–151. https://doi.org/10.1016/j.microc.2012.05.021
Botero-Coy AM, Ibánez M, Sancho JV, Hernández F (2013) Direct liquid chromatography–tandem mass spectrometry determination of underivatized glyphosate in rice, maize and soybean. J Chromatogr A 1313:157–165. https://doi.org/10.1016/j.chroma.2013.07.037
Ogunbiyi OD, Akamo DO, Oluwasanmi EE, Adebanjo J, Isafiade BA, Ogunbiyi TJ, Alli YA, Ayodele DT, Oladoye PO (2023) Glyphosate-based herbicide: Impacts, detection, and removal strategies in environmental samples. Groundw Sustain Dev 22:100961. https://doi.org/10.1016/j.gsd.2023.100961
Huhn C (2018) More and enhanced glyphosate analysis is needed. Anal Bioanal Chem 410:3041–3045. https://doi.org/10.1007/s00216-018-1000-3.49
Duke SO, Powles SB (2008) Glyphosate: a once-in-a-century herbicide. Pest Manag Sci 64:319–325. https://doi.org/10.1002/ps.1518
Villeneuve A, Larroudé S, Humbert JF (2011) Herbicide contamination of freshwater ecosystems: impact on microbial communities. In: Stoytcheva M (ed) Pesticides—formulations, effects, fate. InTech, Rijeka, pp 285–312. https://doi.org/10.5772/13515
Chang FC, Simcik MF, Capel PD (2011) Occurrence and fate of the herbicide glyphosate and its degradate aminomethylphosphonic acid in the atmosphere. Environ Toxicol Chem 30:548–555. https://doi.org/10.1002/etc.431
Silva V, Montanarella L, Jones A, Fernández-Ugalde O, Mol HGJ, Ritsema CJ, Geissen V (2018) Distribution of glyphosate and aminomethylphosphonic acid (AMPA) in agricultural topsoils of the European Union. Sci Total Environ 621:1352–1359. https://doi.org/10.1016/j.scitotenv.2017.10.093
Lutri VF, Matteoda E, Blarasin M, Aparicio V, Giacobone D, Maldonado L, Becher Quinodoz F, Cabrera A, Giuliano Albo J (2020) Hydrogeological features affecting spatial distribution of glyphosate and AMPA in groundwater and surface water in an agroecosystem. Córdoba. Argentina. Sci Total Environ 711:134557. https://doi.org/10.1016/j.scitotenv.2019.134557
Grandcoin A, Piel S, Baurès E (2017) AminoMethylPhosphonic acid (AMPA) in natural waters: its sources, behavior and environmental fate. Weed Res 117:187–197. https://doi.org/10.1016/j.watres.2017.03.055
Pinto E, Soares AG, Ferreira IPMLV (2018) Quantitative analysis of glyphosate, glufosinate and AMPA in irrigation water by in situ derivatization—dispersive liquid-liquid microextraction combined with UPLC-MS/MS. Anal Methods 10:554–561. https://doi.org/10.1039/C7AY02722B
Bonansea RI, Filippi I, Wunderlin DA, Marino DJG, Amé MV (2018) The fate of glyphosate and AMPA in a freshwater endorheic basin: an ecotoxicological risk assessment. Toxics 6:3. https://doi.org/10.3390/toxics6010003
Hanke I, Wittmer I, Bischofberger S, Stamm C, Singer H (2010) Relevance of urban glyphosate use for surface water quality. Chemosphere 81:422–429. https://doi.org/10.1016/j.chemosphere.2010.06.067
Centrum voor Milieuwetenschappen Leiden (2021) Atlas bestrijdingsmiddelen in oppervlaktewater, Universiteit Leiden, Leiden, Netherlands, https://www.bestrijdingsmiddelenatlas.nl/atlas/1/1. Accessed 14 Jan 2024
Poiger T, Buerge IJ, Bächli A, Müller MD, Balmer ME (2017) Occurrence of the herbicide glyphosate and its metabolite AMPA in surface waters in Switzerland determined with on-line solid phase extraction LC-MS/MS. Environ Sci Pollut Res 24:1588–1596. https://doi.org/10.1007/s11356-016-7835-2
Di Guardo A, Finizio A (2018) A new methodology to identify surface water bodies at risk by using pesticide monitoring data: the glyphosate case study in Lombardy Region (Italy). Sci Total Environ 610–611:421–429. https://doi.org/10.1016/j.scitotenv.2017.08.049
Lefrancq M, Jadas-Hécart A, La Jeunesse I, Landry D, Payraudeau S (2017) High frequency monitoring of pesticides in runoff water to improve understanding of their transport and environmental impacts. Sci Total Environ 587–588:75–86. https://doi.org/10.1016/j.scitotenv.2017.02.022
Knepper TP, Berna JL (2003) Surfactants: properties, production, and environmental aspects. Compr Anal Chem 40:1–49. https://doi.org/10.1016/S0166-526X(03)40004-4
Bergé A, Wiest L, Baudot R, Giroud B, Vulliet E (2018) Occurrence of multi-class surfactants in urban wastewater: contribution of a healthcare facility to the pollution transported into the sewerage system. Environ Sci Pollut Res 25:9219–9229. https://doi.org/10.1007/s11356-017-0470-8
Annett R, Habibi HR, Hontela A (2014) Impact of glyphosate and glyphosate-based herbicides on the freshwater environment. J Appl Toxicol 34:458–479. https://doi.org/10.1002/jat.2997
Gonçalves BB, Giaquinto PC, dos Santos Silva D, de Melo e Silva Neto C, de Lima AA, Darosci AAB, Portinho JL, Carvalho WF, Rocha TL (2019) Ecotoxicology of glyphosate-based herbicides on aquatic environment. In: Muharrem I, Olcay Kaplan I, Gabrijel O (eds) Biochemical toxicology. IntechOpen, Rijeka, p 24. https://doi.org/10.5772/intechopen.85157
Mie A, Rudén C (2022) What you don’t know can still hurt you - underreporting in EU pesticide regulation. Environ Health 21:79. https://doi.org/10.1186/s12940-022-00891-7
Dabney BL, Patiño R (2018) Low-dose stimulation of growth of the harmful alga, Prymnesium parvum, by glyphosate and glyphosate-based herbicides. Harmful Algae 80:130–139. https://doi.org/10.1016/j.hal.2018.11.004
Fernández C, Asselborn V, Parodi ER (2021) Toxic effects of chlorpyrifos, cypermethrin and glyphosate on the non-target organism Selenastrum capricornutum (Chlorophyta). An Acad Bras Cienc 93:e20200233. https://doi.org/10.1590/0001-3765202120200233
Reno U, Doyle SR, Momo FR, Regaldo L, Gagneten AM (2018) Effects of glyphosate formulations on the population dynamics of two freshwater cladoceran species. Ecotoxicology 27:784–793. https://doi.org/10.1007/s10646-017-1891-3
Iummato MM, Sabatini SE, Cacciatore LC, Cochón AC, Cataldo D, de Molina MDCR, Juárez ÁB (2018) Biochemical responses of the golden mussel Limnoperna fortunei under dietary glyphosate exposure. Ecotox Environ Saf 163:69–75. https://doi.org/10.1016/j.ecoenv.2018.07.046
Fiorino E, Sehonova P, Plhalova L, Blahova J, Svobodova Z, Faggio C (2018) Effects of glyphosate on early life stages: comparison between Cyprinus carpio and Danio rerio. Environ Sci Pollut Res 25:8542–8549. https://doi.org/10.1007/s11356-017-1141-5
Bach NC, Marino DJG, Natale GS, Somoza GM (2018) Effects of glyphosate and its commercial formulation, Roundup® Ultramax, on liver histology of tadpoles of the neotropical frog, Leptodactylus latrans (amphibia: Anura). Chemosphere 202:289–297. https://doi.org/10.1016/j.chemosphere.2018.03.110
ECHA (2022) Glyphosate. European Chemicals Agency, Helsinki, Finland, https://echa.europa.eu/hu/registry-of-clh-intentions-until-outcome/-/dislist/details/0b0236e185e41a77. Accessed 14 Jan 2024
Webster TMU, Santos EM (2015) Global transcriptomic profiling demonstrates induction of oxidative stress and of compensatory cellular stress responses in brown trout exposed to glyphosate and Roundup. BMC Genomics 16:32. https://doi.org/10.1186/s12864-015-1254-5
Carles L, Gardon H, Joseph L, Sanchís J, Farré M, Artigas J (2019) Meta-analysis of glyphosate contamination in surface waters and dissipation by biofilms. Environ Int 124:284–293. https://doi.org/10.1016/j.envint.2018.12.064
Shaw LE, Mibbayad A (2016) 2,4-D and glyphosate affect aquatic biofilm accrual, gross primary production, and community respiration. AIMS Environ Sci 3:663–672. https://doi.org/10.3934/environsci.2016.4.663
Klátyik Sz, Takács E, Mörtl M, Földi A, Trábert Zs, Ács É, Darvas B, Székács A (2017) Dissipation of the herbicide active ingredient glyphosate in natural water samples in the presence of biofilms. Int J Environ Anal Chem 97:901–921. https://doi.org/10.1080/03067319.2017.1373770
da Costa NB, Fugère V, Hébert M-P, Xu CCY, Barrett RDH, Beisner BE, Bell G, Yargeau V, Fussmann GF, Gonzalez A, Shapiro BJ (2021) Resistance, resilience, and functional redundancy of freshwater bacterioplankton communities facing a gradient of agricultural stressors in a mesocosm experiment. Mol Ecol 30:4771–4788. https://doi.org/10.1111/mec.16100
Characklis WG, Marshall KC (1990) Physiological ecology in biofilm systems. In: Characklis WG, Marshall KC (eds) Biofilms. John Wiley & Sons, New York, pp 341–394
Xiang H, Zhang Y, Atkinson D, Sekar R (2022) Anthropogenic carrion subsidy and herbicide glyphosate depressed leaf-litter breakdown: Effects on environmental health in streams. Front Environ Sci 10:2022. https://doi.org/10.3389/fenvs.2022.806340
Piccini C, Fazi S, Pérez G, Batani G, Martínez de la Escalera G, Sotelo-Silveira JR (2020) Resistance to degradation and effect of the herbicide glyphosate on the bacterioplankton community of a large river system dominated by agricultural activities. Mar Freshw Res 71:1026–1032. https://doi.org/10.1071/MF19079
Lu T, Xu N, Zhang Q, Zhang Z, Debognies A, Zhou Z, Sun L, Qian H (2020) Understanding the influence of glyphosate on the structure and function of freshwater microbial community in a microcosm. Environ Pollut 260:114012. https://doi.org/10.1016/j.envpol.2020.114012
Cornish CM, Bergholz P, Schmidt K, Sweetman J (2023) How benthic sediment microbial communities respond to glyphosate and its metabolite: a microcosm experiment. Microb Ecol 86:2949–2958. https://doi.org/10.1007/s00248-023-02296-6
Wang C, Lin X, Li L, Lin L, Lin S (2017) Glyphosate shapes a dinoflagellate-associated bacterial community while supporting algal growth as sole phosphorus source. Front Microbiol 8:2530. https://doi.org/10.3389/fmicb.2017.02530
Sutherland IW (2001) Biofilm exopolysaccharides: a strong and sticky framework. Microbiology 147:3–9. https://doi.org/10.1099/00221287-147-1-3
Flemming H-C, Wingender J (2010) The biofilm matrix. Nat Rev Microbiol 8:623. https://doi.org/10.1038/nrmicro2415
Niu X, Wang H, Wang T, Zhang P, Zhang H, Wang H, Kong X, Xie S, Xu J (2024) The combination of multiple environmental stressors strongly alters microbial community assembly in aquatic ecosystems. J Environ Manage 350:119594. https://doi.org/10.1016/j.jenvman.2023.119594
Lima IS, Baumeier NC, Rosa RT, Campelo PM, Rosa EA (2014) Influence of glyphosate in planktonic and biofilm growth of Pseudomonas aeruginosa. Braz J Microbiol 45:971–975. https://doi.org/10.1590/s1517-83822014000300029
Turek M, Biczak R, Pawłowska B, Różycka-Sokołowska E, Marciniak B, Deska M, Skalik J, Bałczewski P (2018) Ammonium haloacetates—an alternative to glyphosate? Chemosphere 194:650–656. https://doi.org/10.1016/j.chemosphere.2017.12.055
Sihtmäe M, Blinova I, Künnis-Beres K, Kanarbik L, Heinlaan M, Kahru A (2013) Ecotoxicological effects of different glyphosate formulations. Appl Soil Ecol 72:215–224. https://doi.org/10.1016/j.apsoil.2013.07.005
Bonnet J-L, Bonnemoy F, Dusser M, Bohatier J (2007) Assessment of the potential toxicity of herbicides and their degradation products to nontarget cells using two microorganisms, the bacteria Vibrio fischeri and the ciliate Tetrahymena pyriformis. Environ Toxicol 22:78–91. https://doi.org/10.1002/tox.20237
Manan A, Roytrakul S, Charoenlappanit S, Poolpak T, Ounjai P, Kruatrachue M, Yang KM, Pokethitiyook P (2023) Glyphosate metabolism in Tetrahymena thermophila: a shotgun proteomic analysis approach. Environ Toxicol 38:867–882. https://doi.org/10.1002/tox.23735
Janßen R, Skeff W, Werner J, Wirth MA, Kreikemeyer B, Schulz-Bull D, Labrenz M (2019) A glyphosate pulse to brackish long-term microcosms has a greater impact on the microbial diversity and abundance of planktonic than of biofilm assemblages. Front Mar Sci 6:758. https://doi.org/10.3389/fmars.2019.00758
van Ginkel CG, Stroo CA, Kroon AGM (1993) Biodegradability of ethoxylated fatty amines and amides and the non-toxicity of their biodegradation products. Tenside Surfactants Deterg 30:213–216. https://doi.org/10.1515/tsd-1993-300320
Iummato MM, Fassiano A, Graziano M, Dos Santos AM, Ríos de Molina MDC, Juárez ÁB (2019) Effect of glyphosate on the growth, morphology, ultrastructure and metabolism of Scenedesmus vacuolatus. Ecotoxicol Environ Saf 15:471–479. https://doi.org/10.1016/j.ecoenv.2019.01.083
Smedbol É, Gomes MP, Paquet S, Labrecque M, Lepage L, Lucotte M, Juneau P (2018) Effects of low concentrations of glyphosate-based herbicide factor 540® on an agricultural stream freshwater phytoplankton community. Chemosphere 192:133–141. https://doi.org/10.1016/j.chemosphere.2017.10.128
Smedbol É, Lucotte M, Labrecque M, Lepage L, Juneau P (2017) Phytoplankton growth and PSII efficiency sensitivity to a glyphosate-based herbicide (Factor 540®). Aquat Toxicol 192:265–273. https://doi.org/10.1016/j.aquatox.2017.09.021
Wang C, Lin X, Li L, Lin S (2016) Differential growth responses of marine phytoplankton to herbicide glyphosate. PLoS ONE 11:e0151633. https://doi.org/10.1371/journal.pone.0151633
Ma J, Qin W, Lu N, Wang P, Huang C, Xu R (2005) Differential sensitivity of three cyanobacteria (Anabaena flos-aquae, Microcystis flos-aquae and Mirocystis aeruginosa to 10 pesticide adjuvants. Bull Environ Contam Toxicol 75:873–881. https://doi.org/10.1007/s00128-005-0831-8
Arunakumara K, Walpola B, Yoon M (2013) Metabolism and degradation of glyphosate in aquatic cyanobacteria: a review. Afr J Microbiol Res 7:4084–4090. https://doi.org/10.5897/AJMR12.2302
EGEIS (2020) Aquatic ecotoxicity of glyphosate and formulated products containing glyphosate. European Glyphosate Environmental Information Sources, http://www.egeis.org/cd-info/Aquatic-ecotoxicity-of-glyphosate-and-formulated-products-containing-glyphosate.pdf. Accessed 14 Jan 2024
Giesy JP, Dobson S, Solomon KR (2000) Ecotoxicological risk assessment for Roundup herbicide. Rev Environ Contam Toxicol 167:35–120. https://doi.org/10.1007/978-1-4612-1156-3_2
Lewis KA, Tzilivakis J, Warner DJ, Green A (2016) An international database for pesticide risk assessments and management. Hum Ecol Risk Assess 22:1050–1064. https://doi.org/10.1080/10807039.2015.1133242
MacBean C (2012) The pesticide manual, 16th edn. The British Crop Protection Council, Brighton
Baier F, Gruber E, Hein T, Bondar-Kunze E, Ivanković M, Mentler A, Brühl CA, Spangl B, Zaller JG (2016) Non-target effects of a glyphosate-based herbicide on common toad larvae (Bufo bufo, Amphibia) and associated algae are altered by temperature. PeerJ 4:e2641. https://doi.org/10.7717/peerj.2641
Qu M, Wang L, Xu Q, An J, Mei Y, Liu G (2022) Influence of glyphosate and its metabolite aminomethylphosphonic acid on aquatic plants in different ecological niches. Ecotoxicol Environ Saf 246:114155. https://doi.org/10.1016/j.ecoenv.2022.114155
Hernández-García CI, Martínez-Jerónimo F (2020) Multistressor negative effects on an experimental phytoplankton community. The case of glyphosate and one toxigenic cyanobacterium on Chlorophycean microalgae. Sci Total Environ 717:137186. https://doi.org/10.1016/j.scitotenv.2020.137186
Hernández-García CI, Martínez-Jerónimo F (2023) Changes in the morphology and cell ultrastructure of a microalgal community exposed to a commercial glyphosate formulation and a toxigenic cyanobacterium. Front Microbiol 14:1195776. https://doi.org/10.3389/fmicb.2023.1195776
Drzyzga D, Lipok J (2018) Glyphosate dose modulates the uptake of inorganic phosphate by freshwater cyanobacteria. J Appl Phycol 30:299–309. https://doi.org/10.1007/s10811-017-1231-2
Wu L, Qiu Z, Zhou Y, Du Y, Liu C, Ye J, Hu X (2016) Physiological effects of the herbicide glyphosate on the cyanobacterium Microcystis aeruginosa. Aquat Toxicol 178:72–79. https://doi.org/10.1016/j.aquatox.2016.07.010
Sabio García CA, Schiaffino MR, Lozano VL, Vera MS, Ferraro M, Izaguirre I, Pizarro H (2020) New findings on the effect of glyphosate on autotrophic and heterotrophic picoplankton structure: a microcosm approach. Aquat Toxicol 222:105463. https://doi.org/10.1016/j.aquatox.2020.105463
Sabio García CA, Vera MS, Vinocur A, Graziano M, Miranda C, Pizarro HN (2022) Rethinking the term “glyphosate effect” through the evaluation of different glyphosate-based herbicide effects over aquatic microbial communities. Environ Pollut 292:118382. https://doi.org/10.1016/j.envpol.2021.118382
Sylwestrzak Z, Zgrundo A, Pniewski F (2021) Ecotoxicological studies on the effect of Roundup® (glyphosate formulation) on marine benthic microalgae. Int J Environ Res Public Health 18:884. https://doi.org/10.3390/ijerph18030884
Lipok J, Studnik H, Gruyaert S (2010) The toxicity of Roundup® 360 SL formulation and its main constituents: Glyphosate and isopropylamine towards non-target water photoautotrophs. Ecotoxicol Environ Saf 73:1681–1688. https://doi.org/10.1016/j.ecoenv.2010.08.017
Vera MS, Lagomarsino L, Sylvester M, Pérez GL, Rodriguez P, Mugni H, Sinistro R, Ferraro M, Bonetto C, Zagares H, Pizarro H (2010) New evidences of Roundup® (glyphosate formulation) impact on the periphyton community and the water quality of freshwater ecosystems. Ecotoxicology 19:710–721. https://doi.org/10.1007/s10646-009-0446-7
Gonzalez D, Juárez A, Krug C, Santos M, Vera S (2019) Freshwater periphyton response to technical-grade and two commercial formulations of glyphosate. Ecologia Austral 29:020–027. https://doi.org/10.25260/EA.19.29.1.0.816
Qiu H, Geng J, Ren H, Xia X, Wang X, Yu Y (2013) Physiological and biochemical responses of Microcystis aeruginosa to glyphosate and its Roundup® formulation. J Hazard Mater 248–249:172–176. https://doi.org/10.1016/j.jhazmat.2012.12.033
Saxton MA, Morrow EA, Bourbonniere RA, Wilhelm SW (2011) Glyphosate influence on phytoplankton community structure in Lake Erie. J Great Lakes Res 37:683–690. https://doi.org/10.1016/j.jglr.2011.07.004
Gomes MP, Juneau P (2017) Temperature and light modulation of herbicide toxicity on algal and cyanobacterial physiology. Front Environ Sci 5:50. https://doi.org/10.3389/fenvs.2017.00050
Vera MS, Trinelli MA (2021) First evaluation of the periphyton recovery after glyphosate exposure. Environ Pollut 290:117998. https://doi.org/10.1016/j.envpol.2021.117998
Lozano VL, Vinocur A, y García CAS, Allende L, Cristos DS, Rojas D, Wolansky M, Pizarro H (2018) Effects of glyphosate and 2,4-D mixture on freshwater phytoplankton and periphyton communities: a microcosms approach. Ecotoxicol Environ Saf 148:1010–1019. https://doi.org/10.1016/j.ecoenv.2017.12.006
Wood RJ, Mitrovic SM, Lim RP, Kefford BJ (2016) The influence of reduced light intensity on the response of benthic diatoms to herbicide exposure. Environ Toxicol Chem 35:2252–2260. https://doi.org/10.1002/etc.3379
Bricheux G, Le Moal G, Hennequin C, Coffe G, Donnadieu F, Portelli C, Bohatier J, Forestier C (2013) Characterization and evolution of natural aquatic biofilm communities exposed in vitro to herbicides. Ecotoxicol Environ Saf 88:126–134. https://doi.org/10.1016/j.ecoenv.2012.11.003
Bonnineau C, Sague IG, Urrea G, Guasch H (2012) Light history modulates antioxidant and photosynthetic responses of biofilms to both natural (light) and chemical (herbicides) stressors. Ecotoxicology 21:1208–1224. https://doi.org/10.1007/s10646-012-0876-5
Gattás F, Vinocur A, Graziano M, dos Santos AM, Pizarro H, Cataldo D (2016) Differential impact of Limnoperna fortunei-herbicide interaction between Roundup Max® and glyphosate on freshwater microscopic communities. Environ Sci Pollut Res Int 23:18869–18882. https://doi.org/10.1007/s11356-016-7005-6
De Stefano LG, Gattás F, Vinocur A, Cristos D, Rojas D, Cataldo D, Pizarro H (2018) Comparative impact of two glyphosate-based formulations in interaction with Limnoperna fortunei on freshwater phytoplankton. Ecol Indic 85:575–584. https://doi.org/10.1016/j.ecolind.2017.11.021
Cobb AH, Reade JP (2010) The inhibition of amino acid biosynthesis. In: Cobb A, Reade J (eds) Herbicides and plant physiology. Wiley-Blackwell, Oxford, pp 176–197. https://doi.org/10.1002/9781444327793.ch9
Gomes MP, Le Manac’h SG, Hénault-Ethier L, Labrecque M, Lucotte M, Juneau P (2017) Glyphosate-dependent inhibition of photosynthesis in willow. Front Plant Sci 8:207. https://doi.org/10.3389/fpls.2017.00207
Gomes MP, Le Manac’h SG, Maccario S, Labrecque M, Lucotte M, Juneau P (2016) Differential effects of glyphosate and aminomethylphosphonic acid (AMPA) on photosynthesis and chlorophyll metabolism in willow plants. Pestic Biochem Physiol 130:65–70. https://doi.org/10.1016/j.pestbp.2015.11.010
Choi CJ, Berges JA, Young EB (2012) Rapid effects of diverse toxic water pollutants on chlorophyll a fluorescence: variable responses among freshwater microalgae. Weed Res 46:2615–2626. https://doi.org/10.1016/j.watres.2012.02.027
de Campos OR, Boas LKV, Branco CCZ (2016) Assessment of the potential toxicity of glyphosate-based herbicides on the photosynthesis of Nitella microcarpa var. wrightii (Charophyceae). Phycologia 55:577–584. https://doi.org/10.2216/16-12.1
Jalal A, Oliveira Junior JCd, Ribeiro JS, Fernandes GC, Mariano GG, Trindade VDR, Reis ARd (2021) Hormesis in plants: physiological and biochemical responses. Ecotoxicol Environ Saf 207:111225. https://doi.org/10.1016/j.ecoenv.2020.111225
Rodriguez-Gil JL, Prosser R, Poirier D, Lissemore L, Thompson D, Hanson M, Solomon KR (2017) Aquatic hazard assessment of MON 0818, a commercial mixture of alkylamine ethoxylates commonly used in glyphosate-containing herbicide formulations. Part 1: species sensitivity distribution from laboratory acute exposures. Environ Toxicol Chem 36:512–521. https://doi.org/10.1002/etc.3559
Madsen T, Petersen G, Seierø C, Tørsløv J (1996) Biodegradability and aquatic toxicity of glycoside surfactants and a nonionic alcohol ethoxylate. J Am Oil Chem Soc 73:929–933. https://doi.org/10.1007/BF02517997
Jurado E, Fernández-Serrano M, Núñez Olea J, Lechuga M, Jiménez JL, Ríos F (2012) Acute toxicity of alkylpolyglucosides to Vibrio fischeri, Daphnia magna and microalgae: a comparative study. Bull Environ Contam Toxicol 88:290–295. https://doi.org/10.1007/s00128-011-0479-5
Jeppesen E, Jensen JP, Søndergaard M, Lauridsen T, Pedersen LJ, Jensen L (1997) Top-down control in freshwater lakes: the role of nutrient state, submerged macrophytes and water depth. Hydrobiologia 342:151–164. https://doi.org/10.1023/A:1017046130329
Sobrero C, Martin M, Ronco A (2007) Fitotoxicidad del herbicida Roundup® Max sobre la especie no blanco Lemna gibba en estudios de campo y laboratorio. Hidrobiológica 17:31–39 (ISSN 0188-8897)
Tajnaiová L, Vurm R, Kholomyeva M, Kobera M, Kočí V (2020) Determination of the ecotoxicity of herbicides Roundup® Classic Pro and Garlon New in aquatic and terrestrial environments. Plants (Basel) 9:1203. https://doi.org/10.3390/plants9091203
Kielak E, Sempruch C, Mioduszewska H, Klocek J, Leszczyński B (2011) Phytotoxicity of Roundup Ultra 360 SL in aquatic ecosystems: Biochemical evaluation with duckweed (Lemna minor L.) as a model plant. Pestic Biochem Phys 99:237–243. https://doi.org/10.1016/j.pestbp.2011.01.002
Sikorski Ł, Baciak M, Bęś A, Adomas B (2019) The effects of glyphosate-based herbicide formulations on Lemna minor, a non-target species. Aquat Toxicol 209:70–80. https://doi.org/10.1016/j.aquatox.2019.01.021
Eck-Varanka B, Kováts N, Hubai K, Sainnokhoi T-A (2023) Assessing the effect of glyphosate toxicity on Lemna minor in different temperature regimes. Pollutants 3:451–460. https://doi.org/10.3390/pollutants3040031
Gomes MP, Freitas PL, Kitamura RSA, Pereira EG, Juneau P (2022) How aminomethylphosphonic acid (AMPA), the main glyphosate metabolite, interferes with chlorophyll biosynthesis? Environ Exp Bot 203:105039. https://doi.org/10.1016/j.envexpbot.2022.105039
Mendes EJ, Malage L, Rocha DC, Kitamura RSA, Gomes SMA, Navarro-Silva MA, Gomes MP (2021) Isolated and combined effects of glyphosate and its by-product aminomethylphosphonic acid on the physiology and water remediation capacity of Salvinia molesta. J Hazard Mater 417:125694. https://doi.org/10.1016/j.jhazmat.2021.125694
Diagonel G, Carriel O, de Campos OR, Boas K, Branco C (2022) Effect of glyphosate-based herbicides on the photosynthetic responses of the macrophyte Egeria densa Planch. from topical lotic ecosystems. Limnetica 41:73–84. https://doi.org/10.23818/limn.23841.23806
Hyman LH (1940) The invertebrates. IV. Echinodermata. McGraw-Hill, New York, pp 22–43
Nanieva AV, Pelishenko AV, Kovalenko VF, Goncharuk VV (2019) Hydra attenuata, a model system for determining the acute lethal and chronic toxicity of drinking and natural waters and aqueous solutions of chemicals. J Water Chem Technol 41:329–333. https://doi.org/10.3103/S1063455X19050102
Gabriel A, Venâncio C, Sousa JP, Leston S, Ramos F, Soares AM, Lopes I (2023) Ecotoxicity of eluates obtained from Basamid® contaminated soils is pH dependent: a study with Hydra viridissima, Xenopus laevis and Danio rerio. Sci Total Environ 868:161640. https://doi.org/10.1016/j.scitotenv.2023.161640
Pollino CA, Holdway DA (1999) Potential of two hydra species as standard toxicity test animals. Ecotoxicol Environ Saf 43:309–316. https://doi.org/10.1006/eesa.1999.1796
Venâncio C, Barbosa C, Lopes I (2023) Glyphosate and Roundup® ready effects in Hydra viridissima: new data in an old issue. Sustainability 15:12428. https://doi.org/10.3390/su151612428
Reilly K, Ellis LA, Davoudi HH, Supian S, Maia MT, Silva GH, Guo Z, Martinez DST, Lynch I (2023) Daphnia as a model organism to probe biological responses to nanomaterials-from individual to population effects via adverse outcome pathways. Front Toxicol 5:1178482. https://doi.org/10.3389/ftox.2023.1178482
Toumi H, Boumaiza M, Millet M, Radetski CM, Camara BI, Felten V, Ferard J-F (2015) Investigation of differences in sensitivity between 3 strains of Daphnia magna (crustacean Cladocera) exposed to malathion (organophosphorous pesticide). J Environ Sci Health B 50:34–44. https://doi.org/10.1080/03601234.2015.965617
FAO (2001) Glyphosate N-(phosphonomethyl)glycine. Food and Agriculture Organization Specifications and evaluations for plant protection products. Food and Agriculture Organization of the United Nations, Québec, Canada, http://www.fao.org/fileadmin/templates/agphome/documents/Pests_Pesticides/Specs/glypho01.pdf. Accessed 14 Jan 2024
Islam SS, Midya S (2023) Growth regulatory pattern of zooplankton in herbicide and antibiotic contaminated aquatic ecosystem: an overview. WEE 5:153–160. https://doi.org/10.1016/j.wsee.2023.06.001
Lares BA, Vignatti AM, Echaniz SA, Gutiérrez MF (2022) Effects of glyphosate on cladocera: a synthetic review. Aquat Toxicol 249:106232. https://doi.org/10.1016/j.aquatox.2022.106232
Hernández-Zamora M, Rodríguez-Miguel A, Martínez-Jerónimo L, Martínez-Jerónimo F (2023) Combined toxicity of glyphosate (Faena®) and copper to the american cladoceran Daphnia exilis - a two-generation analysis. Water 15:2018. https://doi.org/10.3390/w15112018
McAllister W, Forbis A (1978) Acute toxicity of technical glyphosate (AB-78–201) to Daphnia magna. United States Environmental Protection Agency, Washington, USA, https://archive.epa.gov/pesticides/chemicalsearch/chemical/foia/web/pdf/103601/103601-1985-08-30b.pdf. Accessed 14 Jan 2024
Forbis A, Boudreau P (1981) Acute toxicity of MON0139 (Lot LURT 12011) (AB-81-074) to Daphnia magna: Static acute bioassay report no. 27203. United States Environmental Protection Agency, Washington, USA, https://www3.epa.gov/pesticides/chem_search/cleared_reviews/csr_PC-103601_30-Aug-85_d.pdf. Accessed 14 Jan 2024
Domínguez-Cortinas G, Saavedra JM, Santos-Medrano GE, Rico-Martínez R (2008) Analysis of the toxicity of glyphosate and Faena® using the freshwater invertebrates Daphnia magna and Lecane quadridentata. Toxicol Environ Chem 90:377–384. https://doi.org/10.1080/02772240701529038
Alberdi JL, Sáenz ME, Di Marzio WD, Tortorelli MC (1996) Comparative acute toxicity of two herbicides, paraquat and glyphosate, to Daphnia magna and D. spinulata. Bull Environ Contam Toxicol 57:229–235. https://doi.org/10.1007/s001289900180
Mel’nichuk SD, Lokhanskaya VI (2007) Estimation of toxicity of glyphosate-based herbicides by biotesting method using cladocera. Hydrobiol J 43:80–91. https://doi.org/10.1615/HydrobJ.v43.i3.60
Pereira JL, Antunes SC, Castro BB, Marques CR, Gonçalves AMM, Gonçalves F, Pereira R (2009) Toxicity evaluation of three pesticides on non-target aquatic and soil organisms: commercial formulation versus active ingredient. Ecotoxicology 18:455–463. https://doi.org/10.1007/s10646-009-0300-y
Ørsted M, Roslev P (2015) A fluorescence-based hydrolytic enzyme activity assay for quantifying toxic effects of Roundup® to Daphnia magna. Environ Toxicol Chem 34:1841–1850. https://doi.org/10.1002/etc.2997
da Silva MLN, Nogueira DJ, Köerich JS, Vaz VP, Justino NM, Schmidt JRA, Vicentini DS, Matias MS, de Jr Castilhos AB, Jr Fuzinatto CF, Matias WG (2021) Multigenerational toxic effects on Daphnia magna induced by silver nanoparticles and glyphosate mixture. Environ Toxicol 40:1123–1131. https://doi.org/10.1002/etc.4952
Cuhra M, Traavik T, Bøhn T (2013) Clone- and age-dependent toxicity of a glyphosate commercial formulation and its active ingredient in Daphnia magna. Ecotoxicology 22:251–262. https://doi.org/10.1007/s10646-012-1021-1
Demetrio PM, Bonetto C, Ronco AE (2014) The effect of cypermethrin, chlorpyrifos, and glyphosate active ingredients and formulations on Daphnia magna (Straus). Bull Environ Contam Toxicol 93:268–273. https://doi.org/10.1007/s00128-014-1336-0
Le T-H, Lim E-S, Lee SK, Choi Y-W, Kim Y-H, Min J (2010) Effects of glyphosate and methidathion on the expression of the Dhb, Vtg, Arnt, CYP4 and CYP314 in Daphnia magna. Chemosphere 79:67–71. https://doi.org/10.1016/j.chemosphere.2009.12.067
Gustinasari K, Sługocki Ł, Czerniawski R, Pandebesie ES, Hermana J (2021) Acute toxicity and morphology alterations of glyphosate-based herbicides to Daphnia magna and Cyclops vicinus. Toxicol Res 37:197–207. https://doi.org/10.1007/s43188-020-00054-1
McCarthy SD, Rafferty SP, Frost PC (2010) Responses of alkaline phosphatase activity to phosphorus stress in Daphnia magna. J Exp Biol 213:256–261. https://doi.org/10.1242/jeb.037788
Gutierrez MF, Battauz Y, Caisso B (2017) Disruption of the hatching dynamics of zooplankton egg banks due to glyphosate application. Chemosphere 171:644–653. https://doi.org/10.1016/j.chemosphere.2016.12.110
Vera MS, Di Fiori E, Lagomarsino L, Sinistro R, Escaray R, Iummato MM, Juárez A, de Molina R, Mdel C, Tell G, Pizarro H (2012) Direct and indirect effects of the glyphosate formulation Glifosato Atanor® on freshwater microbial communities. Ecotoxicology 21:1805–1816. https://doi.org/10.1007/s10646-012-0915-2
Arreguin-Rebolledo U, Páez-Osuna F, Betancourt-Lozano M, Rico-Martínez R (2023) Multi-and transgenerational synergistic effects of glyphosate and chlorpyrifos at environmentally relevant concentrations in the estuarine rotifer Proales similis. Environ Pollut 318:120708. https://doi.org/10.1016/j.envpol.2022.120708
Morgan MA, Griffith CM, Dinges MM, Lyon YA, Julian RR, Larive CK (2019) Evaluating sub-lethal stress from Roundup® exposure in Artemia franciscana using 1H NMR and GC–MS. Aquat Toxicol 212:77–87. https://doi.org/10.1016/j.aquatox.2019.04.023
Darmani H, Al-Saleh DRH (2023) Lower concentrations of the glyphosate-based herbicide Roundup® cause developmental defects in Artemia salina. Environ Toxicol Chem 42:1586–1594. https://doi.org/10.1002/etc.5639
Brausch JM, Beall B, Smith PN (2007) Acute and sub-lethal toxicity of three POEA surfactant formulations to Daphnia magna. Bull Environ Contam Toxicol 78:510–514. https://doi.org/10.1007/s00128-007-9091-0
Rico-Martínez R, Arias-Almeida J, Pérez-Legaspi I, Alvarado-Flores J, Retes-Pruneda J (2012) Adverse effects of herbicides on freshwater zooplankton. In: Hasaneen M (ed) Herbicides—properties, synthesis and control of weeds. IntechOpen, London, pp 405–434. https://doi.org/10.5772/33558
Riera SF, Cohen RA (2016) Alkyl polyglucoside compound influences freshwater plankton community structure in floating field mesocosms. Ecotoxicology 25:1458–1467. https://doi.org/10.1007/s10646-016-1697-8
Mensah PK, Muller WJ, Palmer CG (2011) Acute toxicity of Roundup® herbicide to three life stages of the freshwater shrimp Caridina nilotica (Decapoda: Atyidae). Phys Chem Earth 36:905–909. https://doi.org/10.1016/j.pce.2011.07.071
Avigliano L, Canosa IS, Medesani DA, Rodríguez EM (2018) Effects of glyphosate on somatic and ovarian growth in the estuarine crab Neohelice granulata, during the pre-reproductive period. Water Air Soil Pollut 229:44. https://doi.org/10.1007/s11270-018-3698-0
Canosa IS, Silveyra GR, Avigliano L, Medesani DA, Rodríguez EM (2018) Ovarian growth impairment after chronic exposure to Roundup Ultramax® in the estuarine crab Neohelice granulata. Environ Sci Pollut Res Int 25:1568–1575. https://doi.org/10.1007/s11356-017-0581-2
Hong Y, Yang X, Yan G, Huang Y, Zuo F, Shen Y, Ding Y, Cheng Y (2017) Effects of glyphosate on immune responses and haemocyte DNA damage of Chinese mitten crab, Eriocheir sinensis. Fish Shellfish Immunol 71:19–27. https://doi.org/10.1016/j.fsi.2017.09.062
Yang X, Yu X, Sun N, Shi X, Niu C, Shi A, Cheng Y (2022) Glyphosate-based herbicide causes spermatogenesis disorder and spermatozoa damage of the Chinese mitten crab (Eriocheir sinensis) by affecting testes characteristic enzymes, antioxidant capacities and inducing apoptosis. Toxicol Appl Pharmacol 447:116086. https://doi.org/10.1016/j.taap.2022.116086
Ferreira-Junior DF, Sarmento RA, Saraiva AdS, Pereira RR, Picanço MC, Pestana JLT, Soares AMVM (2017) Low concentrations of glyphosate-based herbicide affects the development of Chironomus xanthus. Water Air Soil Pollut 228:390. https://doi.org/10.1007/s11270-017-3536-9
Xiang H, Zhang Y, Atkinson D, Sekar R (2020) Effects of anthropogenic subsidy and glyphosate on macroinvertebrates in streams. Environ Sci Pollut Res Int 27:21939–21952. https://doi.org/10.1007/s11356-020-08505-w
Janssens L, Stoks R (2017) Stronger effects of Roundup than its active ingredient glyphosate in damselfly larvae. Aquat Toxicol 193:210–216. https://doi.org/10.1016/j.aquatox.2017.10.028
Séguin A, Mottier A, Perron C, Lebel JM, Serpentini A, Costil K (2017) Sub-lethal effects of a glyphosate-based commercial formulation and adjuvants on juvenile oysters (Crassostrea gigas) exposed for 35days. Mar Pollut Bull 117:348–358. https://doi.org/10.1016/j.marpolbul.2017.02.028
Mottier A, Kientz-Bouchart V, Serpentini A, Lebel JM, Jha AN, Costil K (2013) Effects of glyphosate-based herbicides on embryo-larval development and metamorphosis in the Pacific oyster, Crassostrea gigas. Aquat Toxicol 128–129:67–78. https://doi.org/10.1016/j.aquatox.2012.12.002
Milan M, Rovere GD, Smits M, Ferraresso S, Pastore P, Marin MG, Bogialli S, Patarnello T, Bargelloni L, Matozzo V (2018) Ecotoxicological effects of the herbicide glyphosate in non-target aquatic species: transcriptional responses in the mussel Mytilus galloprovincialis. Environ Pollut 237:442–451. https://doi.org/10.1016/j.envpol.2018.02.049
Matozzo V, Fabrello J, Masiero L, Ferraccio F, Finosc L, Pastore P, Di Gangi IM, Bogialli S (2018) Ecotoxicological risk assessment for the herbicide glyphosate to non-target aquatic species: a case study with the mussel Mytilus galloprovincialis. Environ Pollut 233:623–632. https://doi.org/10.1016/j.envpol.2017.10.100
Wathsala RHGR, Folgueras EC, Iuffrida L, Candela M, Gotti R, Fiori J, Franzellitti S (2022) Glyphosate and its breakdown product AMPA elicit cytoprotective responses in haemocytes of the Mediterranean mussel (Mytilus galloprovincialis). Environ Toxicol Pharmacol 96:103997. https://doi.org/10.1016/j.etap.2022.103997
Sandrini JZ, Rola RC, Lopes FM, Buffon HF, Freitas MM, Martins CdMG, da Rosa CE (2013) Effects of glyphosate on cholinesterase activity of the mussel Perna perna and the fish Danio rerio and Jenynsia multidentata: in vitro studies. Aquat Toxicol 130–131:171–173. https://doi.org/10.1016/j.aquatox.2013.01.006
Iori S, Rovere GD, Ezzat L, Smits M, Ferraresso SS, Babbucci M, Marin MG, Masiero L, Fabrello J, Garro E, Carraro L, Cardazzo B, Patarnello T, Matozzo V, Bargelloni L, Milan M (2020) The effects of glyphosate and AMPA on the mediterranean mussel Mytilus galloprovincialis and its microbiota. Environ Res 182:108984. https://doi.org/10.1016/j.envres.2019.108984
Mottier A, Pini JM, Costil K (2014) Effects of a POEA surfactant system (Genamin T-200(®)) on two life stages of the Pacific oyster, Crassostrea gigas. J Toxicol Sci 39:211–215. https://doi.org/10.2131/jts.39.211
Xu Y, Li AJ, Li K, Qin J, Li H (2017) Effects of glyphosate-based herbicides on survival, development and growth of invasive snail (Pomacea canaliculata). Aquat Toxicol 193:136–143. https://doi.org/10.1016/j.aquatox.2017.10.011
Fadhlaoui M, Lavoie I (2021) Effects of temperature and glyphosate on fatty acid composition, antioxidant capacity, and lipid peroxidation in the gastropod Lymneae sp. Water 13:1039. https://doi.org/10.3390/w13081039
Reddy SB, Nolan CJ, Plautz CZ (2018) Disturbances in reproduction and expression of steroidogenic enzymes in aquatic invertebrates exposed to components of the herbicide Roundup. Toxicol Res Appl 2018:2. https://doi.org/10.1177/2397847318805276
Prosser RS, Rodriguez-Gil JL, Solomon KR, Sibley PK, Poirier DG (2017) Effects of the herbicide surfactant MON 0818 on oviposition and viability of eggs of the ramshorn snail (Planorbella pilsbryi). Environ Toxicol Chem 36:522–531. https://doi.org/10.1002/etc.3571
Monte TCdC, Garcia J, Gentile R, de Vasconcellos MC, Souza J, Braga BV, Maldonado A (2016) In vivo and in vitro effects of the herbicide Roundup® on developmental stages of the trematode Echinostoma paraensei. Exp Parasitol 169:43–50. https://doi.org/10.1016/j.exppara.2016.06.012
Lajmanovich RC, Attademo AM, Simoniello MF, Poletta GL, Junges CM, Peltzer PM, Grenón P, Cabagna-Zenklusen MC (2015) Harmful effects of the dermal intake of commercial formulations containing chlorpyrifos, 2,4-D, and glyphosate on the common toad Rhinella arenarum (Anura: Bufonidae). Water Air Soil Pollut 226:427. https://doi.org/10.1007/s11270-015-2695-9
Héritier L, Duval D, Galinier R, Meistertzheim A-L, Verneau O (2017) Oxidative stress induced by glyphosate-based herbicide on freshwater turtles. Environ Toxicol Chem 36:3343–3350. https://doi.org/10.1002/etc.3916
Meng Q-Y, Kang C-Q, Dang W, Melvin SD, Lu H-L (2023) Minor metabolomic disturbances induced by glyphosate-isopropylammonium exposure at environmentally relevant concentrations in an aquatic turtle, Pelodiscus sinensis. Aquat Toxicol 256:106415. https://doi.org/10.1016/j.aquatox.2023.106415
Latorre MA, López González EC, Larriera A, Poletta GL, Siroski PA (2013) Effects of in vivo exposure to Roundup® on immune system of Caiman latirostris. J Immunotoxicol 10:349–354. https://doi.org/10.3109/1547691X.2012.747233
Siroski PA, Poletta GL, Latorre MA, Merchant ME, Ortega HH, Mudry MD (2016) Immunotoxicity of commercial-mixed glyphosate in broad snouted caiman (Caiman latirostris). Chem Biol Interact 244:64–70. https://doi.org/10.1016/j.cbi.2015.11.031
Lanzarin GAB, Félix LM, Fontaínhas-Fernandes A, Monteiro SM, Venâncio C (2023) Effects of glyphosate or glyphosate-based herbicide during the zebrafish life cycle: a review addressing the mechanisms of toxicity. Water 15:2276. https://doi.org/10.3390/w15122276
Modesto KA, Martinez CBR (2010) Roundup® causes oxidative stress in liver and inhibits acetylcholinesterase in muscle and brain of the fish Prochilodus lineatus. Chemosphere 78:294–299. https://doi.org/10.1016/j.chemosphere.2009.10.047
de Menezes CC, da Fonseca MB, Loro VL, Santi A, Cattaneo R, Clasen B, Pretto A, Morsch VM (2011) Roundup effects on oxidative stress parameters and recovery pattern of Rhamdia quelen. Arch Environ Contam Toxicol 60:665–671. https://doi.org/10.1007/s00244-010-9574-6
Lanzarin G, Venâncio C, Félix LM, Monteiro S (2021) Inflammatory, oxidative stress, and apoptosis effects in zebrafish larvae after rapid exposure to a commercial glyphosate formulation. Biomedicines 9:1784. https://doi.org/10.3390/biomedicines9121784
Dumitru G, Ciornea E, Sandu I (2019) Effect of glyphosate herbicide on some hematological and biochemical parameters in Carassius auratus L. Rev Chim 70:518–521. https://doi.org/10.37358/RC.19.2.6947
De Castro BD, Lanés LEK, Godoy RS, Maltchik L, Oliveira GT (2022) Development stage-dependent oxidative stress responses to the exposure to roundup original© in a neotropical annual killifish. Environ Toxicol Pharmacol 95:103976. https://doi.org/10.1016/j.etap.2022.103976
De Souza FJ, Sousa CCN, Da Silva CC, De Sabóia-Morais SMT, Grisolia CK (2013) Mutagenicity and genotoxicity in gill erythrocyte cells of Poecilia reticulata exposed to a glyphosate formulation. Bull Environ Contam Toxicol 91:583–587. https://doi.org/10.1007/s00128-013-1103-7
Leveroni FA, Caffetti JD, Pastori MC (2017) Genotoxic response of blood, gill and liver cells of Piaractus mesopotamicus after an acute exposure to a glyphosate-based herbicide. Caryologia 70:21–28. https://doi.org/10.1080/00087114.2016.1254454
Guilherme S, Santos MA, Barroso C, Gaivão I, Pacheco M (2012) Differential genotoxicity of Roundup® formulation and its constituents in blood cells of fish (Anguilla anguilla): considerations on chemical interactions and DNA damaging mechanisms. Ecotoxicology 21:1381–1390. https://doi.org/10.1007/s10646-012-0892-5
Chanu KR, Mangang YA, Debbarma S, Pandey PK (2023) Effect of glyphosate-based herbicide roundup on hemato-biochemistry of Labeo rohita (Hamilton, 1822) and susceptibility to Aeromonas hydrophila infection. Environ Sci Pollut Res Int 30:110298–110311. https://doi.org/10.1007/s11356-023-29967-8
Terrazas-Salgado L, Yáñez-Rivera B, Llera-Herrera R, García-Gasca A, Alvarado-Cruz I, Betancourt-Lozano M (2022) Transcriptomic signaling in zebrafish (Danio rerio) embryos exposed to environmental concentrations of glyphosate. J Environ Sci Health B 57:775–785. https://doi.org/10.1080/03601234.2022.2115780
Lu J, Wang W, Zhang C, Xu W, Chen W, Tao L, Li Z, Cheng J, Zhang Y (2022) Characterization of glyphosate-induced cardiovascular toxicity and apoptosis in zebrafish. Sci Total Environ 851:158308. https://doi.org/10.1016/j.scitotenv.2022.158308
Ames J, Severo ES, da Costa-Silva DG, Storck TR, do Amaral AMB, Miragem AA, Rosemberg DB, Loro VL (2023) Glyphosate-based herbicide (GBH) causes damage in embryo-larval stages of zebrafish (Danio rerio). Neurotoxicol Teratol 95:107147. https://doi.org/10.1016/j.ntt.2022.107147
Braz-Mota S, Sadauskas-Henrique H, Duarte RM, Val AL, Almeida-Val VMF (2015) Roundup® exposure promotes gills and liver impairments, DNA damage and inhibition of brain cholinergic activity in the Amazon teleost fish Colossoma macropomum. Chemosphere 135:53–60. https://doi.org/10.1016/j.chemosphere.2015.03.042
Nwani CD, Nagpure NS, Kumar R, Kushwaha B, Lakra WS (2013) DNA damage and oxidative stress modulatory effects of glyphosate-based herbicide in freshwater fish, Channa punctatus. Environ Toxicol Pharmacol 36:539–547. https://doi.org/10.1016/j.etap.2013.06.001
Giommi C, Ladisa C, Carnevali O, Maradonna F, Habibi HR (2022) Metabolomic and transcript analysis revealed a sex-specific effect of glyphosate in zebrafish liver. Int J Mol Sci 23:2724. https://doi.org/10.3390/ijms23052724
Liu Z, Shangguan Y, Zhu P, Sultan Y, Feng Y, Li X, Ma J (2022) Developmental toxicity of glyphosate on embryo-larval zebrafish (Danio rerio). Ecotoxicol Environ Saf 236:113493. https://doi.org/10.1016/j.ecoenv.2022.113493
Tóth G, Háhn J, Gy S, Bakos K, Volner C, Liang X, Göbölös B, Bock I, Szoboszlay S, Urbányi B, Kriszt B, Kaszab E, Szabó I, Zs C (2024) In vivo estrogenicity of glyphosate, its formulations, and AMPA on transgenic zebrafish (Danio rerio) embryos. Environ Pollut 342:123113. https://doi.org/10.1016/j.envpol.2023.123113
Cao X, Rao C, Cui H, Sun D, Li L, Guo S, Zhou J, Yuan R, Yang S, Chen J (2022) Toxic effects of glyphosate on the intestine, liver, brain of carp and on epithelioma papulosum cyprinid cells: Evidence from in vivo and in vitro research. Chemosphere 302:134691. https://doi.org/10.1016/j.chemosphere.2022.134691
Lechinovski L, Bados M, Rosa J, Moda DB, Bueno Krawczyk ACD (2022) Ecotoxicological effects of conventional herbicides and a natural herbicide on freshwater fish (Danio rerio). J Environ Sci Health B 57:812–820. https://doi.org/10.1080/03601234.2022.2122664
Armiliato N, Ammar D, Nezzi L, Straliotto M, Muller YM, Nazari EM (2014) Changes in ultrastructure and expression of steroidogenic factor-1 in ovaries of zebrafish Danio rerio exposed to glyphosate. J Toxicol Environ Health A 77:405–414. https://doi.org/10.1080/15287394.2014.880393
Zhang W, Wang J, Song J, Feng Y, Zhang S, Wang N, Liu S, Song Z, Lian K, Kang W (2021) Effects of low-concentration glyphosate and aminomethyl phosphonic acid on zebrafish embryo development. Ecotoxicol Environ Saf 226:112854. https://doi.org/10.1016/j.ecoenv.2021.112854
Webster TMU, Laing LV, Florance H, Santos EM (2014) Effects of glyphosate and its formulation, roundup, on reproduction in zebrafish (Danio rerio). Environ Sci Technol 48:1271–1279. https://doi.org/10.1021/es404258h
Hued AC, Oberhofer S, de los Ángeles Bistoni M, (2012) Exposure to a commercial glyphosate formulation (Roundup®) alters normal gill and liver histology and affects male sexual activity of Jenynsia multidentata (Anablepidae, Cyprinodontiformes). Arch Environ Contam Toxicol 62:107–117. https://doi.org/10.1007/s00244-011-9686-7
Lopes FM, Varela Junior AS, Corcini CD, da Silva AC, Guazzelli VG, Tavares G, da Rosa CE (2014) Effect of glyphosate on the sperm quality of zebrafish Danio rerio. Aquat Toxicol 155:322–326. https://doi.org/10.1016/j.aquatox.2014.07.006
Sulukan E, Köktürk M, Ceylan H, Beydemir Ş, Işik M, Atamanalp M, Ceyhun SB (2017) An approach to clarify the effect mechanism of glyphosate on body malformations during embryonic development of zebrafish (Danio rerio). Chemosphere 180:77–85. https://doi.org/10.1016/j.chemosphere.2017.04.018
Jin J, Kurobe T, Ramírez-Duarte WF, Bolotaolo MB, Lam CH, Pandey PK, Hung T-C, Stillway ME, Zweig L, Caudill J, Lin L, Teh SJ (2018) Sub-lethal effects of herbicides penoxsulam, imazamox, fluridone and glyphosate on Delta Smelt (Hypomesus transpacificus). Aquat Toxicol 197:79–88. https://doi.org/10.1016/j.aquatox.2018.01.019
Kale OE, Adebesin AN, Kale TF, Oladoja F, Osonuga IO, Soyinka OO, Uwaezuoke D, Olajide O, Akinloye V, Adedugbe O, Odibosa F, Akindele F, Oladele B, Wahab M, Ebele CC (2023) Effects of glyphosate-based herbicide on gametes fertilization and four developmental stages in Clarias gariepinus. Heliyon 9:e15048. https://doi.org/10.1016/j.heliyon.2023.e15048
Du-Carrée JL, Morin T, Danion M (2021) Impact of chronic exposure of rainbow trout, Oncorhynchus mykiss, to low doses of glyphosate or glyphosate-based herbicides. Aquat Toxicol 230:105687. https://doi.org/10.1016/j.aquatox.2020.105687
Bonifacio AF, Cazenave J, Bacchetta C, Ballesteros ML, de los Ángeles Bistoni M, Amé MV, Bertrand L, Hued AC, (2016) Alterations in the general condition, biochemical parameters and locomotor activity in Cnesterodon decemmaculatus exposed to commercial formulations of chlorpyrifos, glyphosate and their mixtures. Ecol Indic 67:88–97. https://doi.org/10.1016/j.ecolind.2016.02.011
Menéndez-Helman RJ, Ferreyroa GV, dos Santos AM, Salibián A (2012) Glyphosate as an acetylcholinesterase inhibitor in Cnesterodon decemmaculatus. Bull Environ Contam Toxicol 88:6–9. https://doi.org/10.1007/s00128-011-0423-8
Cattaneo R, Clasen B, Loro VL, de Menezes CC, Pretto A, Baldisserotto B, Santi A, de Avila LA (2011) Toxicological responses of Cyprinus carpio exposed to a commercial formulation containing glyphosate. Bull Environ Contam Toxicol 87:597–602. https://doi.org/10.1007/s00128-011-0396-7
Murussi CR, Costa MD, Leitemperger JW, Guerra L, Rodrigues CCR, Menezes CC, Severo ES, Flores-Lopes F, Salbego J, Loro VL (2016) Exposure to different glyphosate formulations on the oxidative and histological status of Rhamdia quelen. Fish Physiol Biochem 42:445–455. https://doi.org/10.1007/s10695-015-0150-x
Antunes AM, Rocha TL, Pires FS, de Freitas MA, Leite VRMC, Arana S, Moreira PC, Sabóia-Morais SMT (2017) Gender-specific histopathological response in guppies Poecilia reticulata exposed to glyphosate or its metabolite aminomethylphosphonic acid. J Appl Toxicol 37:1098–1107. https://doi.org/10.1002/jat.3461
Sinhorin VDG, Sinhorin AP, Teixeira JMS, Miléski KML, Hansen PC, Moeller PR, Moreira PSA, Baviera AM, Loro VL (2014) Metabolic and behavior changes in surubim acutely exposed to a glyphosate-based herbicide. Arch Environ Contam Toxicol 67:659–667. https://doi.org/10.1007/s00244-014-0073-z
Bridi D, Altenhofen S, Gonzalez JB, Reolon GK, Bonan CD (2017) Glyphosate and Roundup® alter morphology and behavior in zebrafish. Toxicology 392:32–39. https://doi.org/10.1016/j.tox.2017.10.007
Yalsuyi AM, Vajargah MF, Hajimoradloo A, Galangash MM, Prokić MD, Faggio C (2021) Evaluation of behavioral changes and tissue damages in common carp (Cyprinus carpio) after exposure to the herbicide glyphosate. Vet Sci 8:218. https://doi.org/10.3390/vetsci8100218
Muhammad UA, Yasid NA, Daud HM, Shukor MY (2021) Glyphosate herbicide induces changes in the growth pattern and somatic indices of crossbred red tilapia (O. niloticus × O. mossambicus). Animals 11:1209. https://doi.org/10.3390/ani11051209
Rocha TL, Santos APRd, Yamada ÁT, Soares CMdA, Borges CL, Bailão AM, Sabóia-Morais SMT (2015) Proteomic and histopathological response in the gills of Poecilia reticulata exposed to glyphosate-based herbicide. Environ Toxicol Pharmacol 40:175–186. https://doi.org/10.1016/j.etap.2015.04.016
Chen J, Rao C, Yuan R, Sun D, Guo S, Li L, Yang S, Qian D, Lu R, Cao X (2022) Long-term exposure to polyethylene microplastics and glyphosate interferes with the behavior, intestinal microbial homeostasis, and metabolites of the common carp (Cyprinus carpio L.). Sci Total Environ 814:152681. https://doi.org/10.1016/j.scitotenv.2021.152681
Jia R, Hou Y, Feng W, Li B, Zhu J (2022) Alterations at biochemical, proteomic and transcriptomic levels in liver of tilapia (Oreochromis niloticus) under chronic exposure to environmentally relevant level of glyphosate. Chemosphere 294:133818. https://doi.org/10.1016/j.chemosphere.2022.133818
Søfteland L, Olsvik PA (2022) In vitro toxicity of glyphosate in Atlantic salmon evaluated with a 3D hepatocyte-kidney co-culture model. Food Chem Toxicol 164:113012. https://doi.org/10.1016/j.fct.2022.113012
Ivantsova E, Wengrovitz AS, Souders CL, Martyniuk CJ (2022) Developmental and behavioral toxicity assessment of glyphosate and its main metabolite aminomethylphosphonic acid (AMPA) in zebrafish embryos/larvae. Environ Toxicol Pharmacol 93:103873. https://doi.org/10.1016/j.etap.2022.103873
Abdelmagid AD, Said AM, Abd El-Gawad EA, Shalaby SA, Dawood MAO (2022) Glyphosate-induced liver and kidney dysfunction, oxidative stress, immunosuppression in Nile tilapia, but ginger showed a protection role. Vet Res Commun. https://doi.org/10.1007/s11259-022-09961-0
Alvarado-Suárez GB, Silva-Briano M, Arzate-Cárdenas MA, Carbajal-Hernández AL, Yáñez-Rivera B, Rico-Martínez R (2022) Feeding behavior of early life stages of the zebrafish Danio rerio is altered by exposure to glyphosate. Environ Sci Pollut Res Int 29:85172–85184. https://doi.org/10.1007/s11356-022-21790-x
Navarro CDC, Martinez CBR (2014) Effects of the surfactant polyoxyethylene amine (POEA) on genotoxic, biochemical and physiological parameters of the freshwater teleost Prochilodus lineatus. Comp Biochem Physiol C 165:83–90. https://doi.org/10.1016/j.cbpc.2014.06.003
de Brito RL, Costa GG, Thá EL, da Silva LR, de Oliveira R, Leme DM, Cestari MM, Grisolia CK, Valadares MC, de Oliveira GAR (2019) Impact of the glyphosate-based commercial herbicide, its components and its metabolite AMPA on non-target aquatic organisms. Mutat Res Genet Toxicol Environ Mutagen 842:94–101. https://doi.org/10.1016/j.mrgentox.2019.05.002
Wagner N, Reichenbecher W, Teichmann H, Tappeser B, Lötters S (2013) Questions concerning the potential impact of glyphosate-based herbicides on amphibians. Environ Toxicol Chem 32:1688–1700. https://doi.org/10.1002/etc.2268
European Commission (2021) Commission Regulation (EU) 2021/383 of 3 March 2021 amending Annex III to Regulation (EC) No 1107/2009 of the European Parliament and of the Council listing co-formulants which are not accepted for inclusion in plant protection products. OJ EU L74:7-26. https://eur-lex.europa.eu/legal-content/EN/TXT/?uri=CELEX:32021R0383. Accessed 14 Jan 2024.
Ockleford C, Adriaanse P, Berny P, Brock T, Duquesne S, Grilli S, Hernandez-Jerez AF, Bennekou SH, Klein M, Laskowski TKR, Machera K, Pelkonen O, Pieper S, Stemmer M, Sundh I, Teodorovic I, Tiktak A, Topping CJ, Wolterink G, Aldrich A, Berg C, Ortiz-Santaliestra M, Weir S, Streissl F, Smith RH (2018) Scientific opinion on the state of the science on pesticide risk assessment for amphibians and reptiles. EFSA J 16:5125. https://doi.org/10.2903/j.efsa.2018.5125
Navarro-Martín L, Lanctôt C, Jackman P, Park BJ, Doe K, Pauli BD, Trudeau VL (2014) Effects of glyphosate-based herbicides on survival, development, growth and sex ratios of wood frogs (Lithobates sylvaticus) tadpoles. I: chronic laboratory exposures to VisionMax®. Aquat Toxicol 154:278–290. https://doi.org/10.1016/j.aquatox.2014.05.017
Meza-Joya FL, Ramírez-Pinilla MP, Fuentes-Lorenzo JL (2013) Toxic, cytotoxic, and genotoxic effects of a glyphosate formulation (Roundup®SL—Cosmoflux®411F) in the direct-developing frog Eleutherodactylus johnstonei. Environ Mol Mutagen 54:362–373. https://doi.org/10.1002/em.21775
Rissoli RZ, Abdalla FC, Costa MJ, Rantin FT, McKenzie DJ, Kalinin AL (2016) Effects of glyphosate and the glyphosate based herbicides Roundup Original® and Roundup Transorb® on respiratory morphophysiology of bullfrog tadpoles. Chemosphere 156:37–44. https://doi.org/10.1016/j.chemosphere.2016.04.083
Hedberg D, Wallin M (2010) Effects of Roundup and glyphosate formulations on intracellular transport, microtubules and actin filaments in Xenopus laevis melanophores. Toxicol In Vitro 24:795–802. https://doi.org/10.1016/j.tiv.2009.12.020
Baier F, Jedinger M, Gruber E, Zaller JG (2016) Temperature-dependence of glyphosate-based herbicide’s effects on egg and tadpole growth of common toads. Front Environ Sci 4:51. https://doi.org/10.3389/fenvs.2016.00051
Tartu S, Renoirt M, Cheron M, Gisselmann L-L, Catoire S, Brischoux F (2022) Did decades of glyphosate use have selected for resistant amphibians in agricultural habitats? Environ Pollut 310:119823. https://doi.org/10.1016/j.envpol.2022.119823
Cheron M, Brischoux F (2020) Aminomethylphosphonic acid alters amphibian embryonic development at environmental concentrations. Environ Res 190:109944. https://doi.org/10.1016/j.envres.2020.109944
Relyea RA (2012) New effects of Roundup on amphibians: Predators reduce herbicide mortality; herbicides induce antipredator morphology. Ecol Appl 22:634–647. https://doi.org/10.1890/11-0189.1
Pérez-Iglesias JM, Franco-Belussi L, Moreno L, Tripole S, de Oliveira C, Natale GS (2016) Effects of glyphosate on hepatic tissue evaluating melanomacrophages and erythrocytes responses in neotropical anuran Leptodactylus latinasus. Environ Sci Pollut Res 23:9852–9861. https://doi.org/10.1007/s11356-016-6153-z
Herek JS, Vargas L, Trindade SAR, Rutkoski CF, Macagnan N, Hartmann PA, Hartmann MT (2020) Can environmental concentrations of glyphosate affect survival and cause malformation in amphibians? Effects from a glyphosate-based herbicide on Physalaemus cuvieri and P. gracilis (Anura: Leptodactylidae). Environ Sci Pollut Res Int 27:22619–22630. https://doi.org/10.1007/s11356-020-08869-z
Bach NC, Natale GS, Somoza GM, Ronco AE (2016) Effect on the growth and development and induction of abnormalities by a glyphosate commercial formulation and its active ingredient during two developmental stages of the South-American Creole frog, Leptodactylus latrans. Environ Sci Pollut Res 23:23959–23971. https://doi.org/10.1007/s11356-016-7631-z
Babalola OO, Van Wyk JH (2018) Comparative early life stage toxicity of the African clawed frog, Xenopus laevis following exposure to selected herbicide formulations applied to eradicate alien plants in South Africa. Arch Environ Contam Toxicol 75:8–16. https://doi.org/10.1007/s00244-017-0463-0
Turhan DÖ, Güngördü A, Ozmen M (2020) Developmental and lethal effects of glyphosate and a glyphosate-based product on Xenopus laevis embryos and tadpoles. Bull Environ Contam Toxicol 104:173–179. https://doi.org/10.1007/s00128-019-02774-z
Flach H, Lenz A, Pfeffer S, Kühl M, Kühl SJ (2022) Impact of glyphosate-based herbicide on early embryonic development of the amphibian Xenopus laevis. Aquat Toxicol 244:106081. https://doi.org/10.1016/j.aquatox.2022.106081
Babalola OO, Truter JC, van Wyk JH (2021) Impacts of three glyphosate formulations on gonadal development of Xenopus laevis. Toxic Res Appl 2021:5. https://doi.org/10.1177/23978473211031467
Yadav SS, Giri S, Singha U, Boro F, Giri A (2013) Toxic and genotoxic effects of Roundup on tadpoles of the Indian skittering frog (Euflictis cyanophlyctis) in the presence and absence of predator stress. Aquat Toxicol 132–133:1–8. https://doi.org/10.1016/j.aquatox.2013.01.016
Bonfanti P, Saibene M, Bacchetta R, Mantecca P, Colombo A (2018) A glyphosate micro-emulsion formulation displays teratogenicity in Xenopus laevis. Aquat Toxicol 195:103–113. https://doi.org/10.1016/j.aquatox.2017.12.007
Daam MA, Moutinho MF, Espíndola ELG, Schiesari L (2019) Lethal toxicity of the herbicides acetochlor, ametryn, glyphosate and metribuzin to tropical frog larvae. Ecotoxicology 28:707–715. https://doi.org/10.1007/s10646-019-02067-5
Carvalho WF, Franco FC, Godoy FR, Folador D, Avelar JB, Nomura F, da Cruz AD, de Sabóia-Morais SMT, Bastos RP, de Melo e Silva D (2018) Evaluation of genotoxic and mutagenic effects of glyphosate Roundup Original® in Dendropsophus minutus Peters, 1872 tadpoles. S Am J Herpetol 13:220–229. https://doi.org/10.2994/SAJH-D-17-00016.1
Mikó Z, Ujszegi J, Gál Z, Hettyey A (2017) Effects of a glyphosate-based herbicide and predation threat on the behaviour of agile frog tadpoles. Ecotoxicol Environ Saf 140:96–102. https://doi.org/10.1016/j.ecoenv.2017.02.032
Lajmanovich RC, Attademo AM, Peltzer PM, Junges CM, Cabagna MC (2011) Toxicity of four herbicide formulations with glyphosate on Rhinella arenarum (Anura: Bufonidae) tadpoles: B-esterases and glutathione S-transferase inhibitors. Arch Environ Contam Toxicol 60:681–689. https://doi.org/10.1007/s00244-010-9578-2
Bókony V, Mikó Z, Móricz ÁM, Krüzselyi D, Hettyey A (2017) Chronic exposure to a glyphosate-based herbicide makes toad larvae more toxic. Proc Royal Soc B 284:20170493. https://doi.org/10.1098/rspb.2017.0493
Edge C, Thompson D, Hao C, Houlahan J (2014) The response of amphibian larvae to exposure to a glyphosate-based herbicide (Roundup WeatherMax) and nutrient enrichment in an ecosystem experiment. Ecotoxicol Environ Saf 109:124–132. https://doi.org/10.1016/j.ecoenv.2014.07.040
Levis NA, Johnson JR (2015) Level of UV-B radiation influences the effects of glyphosate-based herbicide on the spotted salamander. Ecotoxicology 24:1073–1086. https://doi.org/10.1007/s10646-015-1448-2
Gandhi JS, Cecala KK (2016) Interactive effects of temperature and glyphosate on the behavior of blue ridge two-lined salamanders (Eurycea wilderae). Environ Toxicol Chem 35:2297–2303. https://doi.org/10.1002/etc.3398
Lopes A, Benvindo-Souza M, Carvalho WF, Nunes HF, de Lima PN, Costa MS, Benetti EJ, Guerra V, Saboia-Morais SMT, Santos CE, Simões K, Bastos RP, de Melo E, Silva D (2021) Evaluation of the genotoxic, mutagenic, and histopathological hepatic effects of polyoxyethylene amine (POEA) and glyphosate on Dendropsophus minutus tadpoles. Environ Pollut 289:117911. https://doi.org/10.1016/j.envpol.2021.117911
Henao Muñoz LM, Montes Rojas CM, Bernal Bautista MH (2015) Acute toxicity and sublethal effects of the mixture glyphosate (Roundup Active) and Cosmo-Flux 411F to anuran embryos and tadpoles of four Colombian species. Rev Biol Trop 63:223–233. https://doi.org/10.15517/rbt.v63i1.12893
Moore LJ, Fuentes L, Rodgers JH, Bowerman WW, Yarrow GK, Chao WY, Bridges WC (2012) Relative toxicity of the components of the original formulation of Roundup® to five North American anurans. Ecotoxicol Environ Saf 78:128–133. https://doi.org/10.1016/j.ecoenv.2011.11.025
Mikó Z, Hettyey A (2023) Toxicity of POEA-containing glyphosate-based herbicides to amphibians is mainly due to the surfactant, not to the active ingredient. Ecotoxicology 32:150–159. https://doi.org/10.1007/s10646-023-02626-x
Banaee M, Akhlaghi M, Soltanian S, Sureda A, Gholamhosseini A, Rakhshaninejad M (2020) Combined effects of exposure to sub-lethal concentration of the insecticide chlorpyrifos and the herbicide glyphosate on the biochemical changes in the freshwater crayfish Pontastacus leptodactylus. Ecotoxicology 29:1500–1515. https://doi.org/10.1007/s10646-020-02233-0
Zhang D, Ding W, Liu W, Li L, Zhu G, Ma J (2023) Single and combined effects of chlorpyrifos and glyphosate on the brain of common carp: based on biochemical and molecular perspective. Int J Mol Sci 24:12934. https://doi.org/10.3390/ijms241612934
Soloneski S, Ruiz de Arcaute C, Larramendy ML (2016) Genotoxic effect of a binary mixture of dicamba- and glyphosate-based commercial herbicide formulations on Rhinella arenarum (Hensel, 1867) (Anura, Bufonidae) late-stage larvae. Environ Sci Pollut Res Int 23:17811–17821. https://doi.org/10.1007/s11356-016-6992-7
Carvalho WF, Ruiz de Arcaute C, Pérez-Iglesias JM, Laborde MRR, Soloneski S, Larramendy ML (2019) DNA damage exerted by mixtures of commercial formulations of glyphosate and imazethapyr herbicides in Rhinella arenarum (Anura, Bufonidae) tadpoles. Ecotoxicology 28:367–377. https://doi.org/10.1007/s10646-019-02029-x
Maggi F, Tang FHM, la Cecilia D, McBratney A (2019) PEST-CHEMGRIDS, global gridded maps of the top 20 crop-specific pesticide application rates from 2015 to 2025. Sci Data 6:170. https://doi.org/10.1038/s41597-019-0169-4
Chahal GS, Johnson WG (2012) Influence of glyphosate or glufosinate combinations with growth regulator herbicides and other agrochemicals in controlling glyphosate-resistant weeds. Weed Technol 26:638–643. https://doi.org/10.1614/WT-D-12-00058.1
Takano HK, Oliveira Junior RS, Constatin J, Biffe DF, Franchini LHM, Braz GBP, Rios FA, Gheno EA, Gemelli A (2013) Effect of 2.4-D addition to glyphosate for difficult control weeds species. Weed Control J 12:1–13. https://doi.org/10.7824/rbh.v12i1.207
Loos R, Locoro G, Contini S (2010) Occurrence of polar organic contaminants in the dissolved water phase of the Danube River and its major tributaries using SPE-LC-MS2 analysis. Water Res 44:2325–2335. https://doi.org/10.1016/j.watres.2009.12.035
Mahler BJ, van Metre PC, Burley TE, Loftin KA, Meyer MT, Nowell LH (2017) Similarities and differences in occurrence and temporal fluctuations in glyphosate and atrazine in small Midwestern streams (USA) during the 2013 growing season. Sci Total Environ 579:149–158. https://doi.org/10.1016/j.scitotenv.2016.10.236
Aparicio VC, de Gerónimo E, Marino D, Primost J, Carriquiriborde P, Costa JL (2013) Environmental fate of glyphosate and aminomethylphosphonic acid in surface waters and soil of agricultural basins. Chemosphere 93:1866–1873. https://doi.org/10.1016/j.chemosphere.2013.06.041
Islam F, Wang J, Farooq MA, Khan MSS, Xu L, Zhu J, Zhao M, Munos S, Li QX, Zhou W (2018) Potential impact of the herbicide 2,4-dichlorophenoxyacetic acid on human and ecosystems. Environ Int 111:332–351. https://doi.org/10.1016/j.envint.2017.10.020
Pavan FA, Samojeden CG, Rutkoski CF, Folador A, Da Fré SP, Müller C, Hartmann PA, Hartmann MT (2021) Morphological, behavioral and genotoxic effects of glyphosate and 2,4-D mixture in tadpoles of two native species of South American amphibians. Environ Toxicol Pharmacol 85:103637. https://doi.org/10.1016/j.etap.2021.103637
Castro MJL, Ojeda C, Cirelli AF (2014) Advances in surfactants for agrochemicals. Environ Chem Lett 12:85–89. https://doi.org/10.1007/s10311-013-0432-4
Song HY, Kim YH, Seok SJ, Gil HW, Hong SY (2012) In vitro cytotoxic effect of glyphosate mixture containing surfactants. J Korean Med Sci 27:711–715. https://doi.org/10.3346/jkms.2012.27.7.711
Peillex C, Pelletier M (2020) The impact and toxicity of glyphosate and glyphosate-based herbicides on health and immunity. J Immunotoxicol 17:163–174. https://doi.org/10.1080/1547691X.2020.1804492
Liu N, Zhong G, Zhou J, Liu Y, Pang Y, Cai H, Wu Z (2019) Separate and combined effects of glyphosate and copper on growth and antioxidative enzymes in Salvinia natans (L.). Sci Total Environ 655:1448–1456. https://doi.org/10.1016/j.scitotenv.2018.11.213
Tremearne T, Jacob K (1941) Arsenic in natural phosphates and phosphate fertilizer. United States Department of Agriculture, Washington. Tech Bull 781.
Jungers G, Portet-Koltalo F, Cosme J, Seralini G-E (2022) Petroleum in pesticides: a Need to change regulatory toxicology. Toxics 10:670. https://doi.org/10.3390/toxics10110670
Collom C, Pradhan SH, Liu JY, Liu J, Sharma V, Sayes CM (2023) Toxicity of binary mixtures of copper, lead, and glyphosate on neuronal cells. J Hazard Mater Adv 11:100355. https://doi.org/10.1016/j.hazadv.2023.100355
Trigueiro NSdS, Gonçalves BB, Dias FC, de Oliveira Lima EC, Rocha TL, Sabóia-Morais SMT (2021) Co-exposure of iron oxide nanoparticles and glyphosate-based herbicide induces DNA damage and mutagenic effects in the guppy (Poecilia reticulata). Environ Toxicol Pharmacol 81:103521. https://doi.org/10.1016/j.etap.2020.103521
Abdelmagid AD, Said AM, Gawad EAA, Shalaby SA, Dawood MAO (2022) Propolis nanoparticles relieved the impacts of glyphosate-induced oxidative stress and immunosuppression in Nile tilapia. Environ Sci Pollut Res Int 29:19778–19789. https://doi.org/10.1007/s11356-021-17201-2
Martins LKL, Lima-Faria JM, Guimarães LN, Silva VCD, Moreira PC, Sabóia-Morais SMT (2022) Co-exposure of iron oxide nanoparticles and glyphosate-based herbicide promote liver toxicity in guppy (Poecilia reticulata): a histochemical and ultrastructural approach. Environ Toxicol 37:2244–2258. https://doi.org/10.1002/tox.23591
Zhang Q, Qu Q, Lu T, Ke M, Zhu Y, Zhang M, Zhang Z, Du B, Pan X, Sun L, Qian H (2018) The combined toxicity effect of nanoplastics and glyphosate on Microcystis aeruginosa growth. Environ Pollut 243:1106–1112. https://doi.org/10.1016/j.envpol.2018.09.073
Nogueira DJ, Silva ACdOd, da Silva MLN, Vicentini DS, Matias WG (2022) Individual and combined multigenerational effects induced by polystyrene nanoplastic and glyphosate in Daphnia magna (Strauss, 1820). Sci Total Environ 811:151360. https://doi.org/10.1016/j.scitotenv.2021.151360
Zocchi M, Sommaruga R (2019) Microplastics modify the toxicity of glyphosate on Daphnia magna. Sci Total Environ 697:134194. https://doi.org/10.1016/j.scitotenv.2019.134194
Le Du-Carrée J, Cabon J, Louboutin L, Morin T, Danion M (2022) Changes in defense capacity to infectious hematopoietic necrosis virus (IHNv) in rainbow trout intergenerationally exposed to glyphosate. Fish Shellfish Immunol 122:67–70. https://doi.org/10.1016/j.fsi.2021.12.021
Le Du-Carrée J, Cabon J, Morin T, Danion M (2021) Immunological and metabolic effects of acute sublethal exposure to glyphosate or glyphosate-based herbicides on juvenile rainbow trout, Oncorhynchus mykiss. Sci Total Environ 784:147162. https://doi.org/10.1016/j.scitotenv.2021.147162
Kelly DW, Poulin R, Tompkins DM, Townsend CR (2010) Synergistic effects of glyphosate formulation and parasite infection on fish malformations and survival. J Appl Ecol 47:498–504. https://doi.org/10.1111/j.1365-2664.2010.01791.x
EFSA, Alvarez F, Arena M, Auteri D, Binaglia M, Castoldi AF, Chiusolo A, Crivellente F, Egsmose M, Fait G, Ferilli F, Gouliarmou V, Nogareda LH, Ippolito A, Istace F, Jarrah S, Kardassi D, Kienzler A, Lanzoni A, Lava R, Linguadoca A, Lythgo C, Mangas I, Padovani L, Panzarea M, Parra Morte JM, Rizzuto S, Romac A, Rortais A, Serafimova R, Sharp R, Cs S, Terron A, Theobald A, Tiramani M, Vianello G, Villamar-Bouza L (2023) Peer review of the pesticide risk assessment of the active substance glyphosate. EFSA J 21:1–52. https://doi.org/10.2903/j.efsa.2023.8164
PAN Europe (2023) Glyphosate in the EU up to 2034? Danger to health and environment and violation of citizens will. https://www.pan-europe.info/press-releases/2023/09/glyphosate-eu-2034-danger-health-and-environment-and-violation-citizens-will. Accessed 14 Jan 2024
European Commission (2023) Commission Implementing Regulation (EU) 2023/2660 of 28 November 2023 renewing the approval of the active substance glyphosate in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council and amending Commission Implementing Regulation (EU) No 540/2011. OJ EU L:2023:2660. http://data.europa.eu/eli/reg_impl/2023/2660/oj. Accessed 14 Jan 2024
Klátyik Sz, Simon G, Oláh M, Mesnage R, Antoniou MN, Zaller JG, Székács A (2023) Terrestrial ecotoxicity of glyphosate, its formulations, and co-formulants: evidence from 2010–2023. Environ Sci Eur 35:51. https://doi.org/10.1186/s12302-023-00758-9
Mesnage R, Teixeira M, Mandrioli D, Falcioni L, Ducarmon QR, Zwittink RD, Mazzacuva F, Caldwell A, Halket J, Amiel C, Panoff JM, Belpoggi F, Antoniou MN (2021) Use of shotgun metagenomics and metabolomics to evaluate the impact of glyphosate or Roundup MON 52276 on the gut microbiota and serum metabolome of Sprague-Dawley rats. Environ Health Perspect 129:17005. https://doi.org/10.1289/ehp6990
Rainio MJ, Margus A, Tikka S, Helander M, Lindström L (2023) The effects of short-term glyphosate-based herbicide exposure on insect gene expression profiles. J Insect Physiol 146:104503. https://doi.org/10.1016/j.jinsphys.2023.104503
Bertram MG, Martin JM, McCallum ES, Alton LA, Brand JA, Brooks BW, Cerveny D, Fick J, Ford AT, Hellström G, Michelangeli M, Nakagawa S, Polverino G, Saaristo M, Sih A, Tan H, Tyler CR, Wong BBM, Brodin T (2022) Frontiers in quantifying wildlife behavioural responses to chemical pollution. Biol Rev Camb Philos Soc 97:1346–1364. https://doi.org/10.1111/brv.12844
Thoré ES, Philippe C, Brendonck L, Pinceel T (2021) Towards improved fish tests in ecotoxicology-efficient chronic and multigenerational testing with the killifish Nothobranchius furzeri. Chemosphere 273:129697. https://doi.org/10.1016/j.chemosphere.2021.129697
Talyn B, Muller K, Mercado C, Gonzalez B, Bartels K (2023) The herbicide glyphosate and its formulations impact animal behavior across taxa. Agrochemicals 2:367–408. https://doi.org/10.3390/agrochemicals2030022
Lopes AR, Moraes JS, Martins CMG (2022) Effects of the herbicide glyphosate on fish from embryos to adults: a review addressing behavior patterns and mechanisms behind them. Aquat Toxicol 251:106281. https://doi.org/10.1016/j.aquatox.2022
Asnicar D, Cappelli C, Sallehuddin AS, Maznan NA, Marin MG (2020) Effects of glyphosate-based and derived products on sea urchin larval development. J Mar Sci Eng 8:661. https://doi.org/10.3390/jmse8090661
European Food Safety Authority (2015) Conclusion on the peer review of the pesticide risk assessment of the active substance glyphosate. EFSA J 13:4302, 107. https://doi.org/10.2903/j.efsa.2015.4302
Brühl CA, Zaller JG (2021) Indirect herbicide effects on biodiversity, ecosystem functions, and interactions with global changes. In: Mesnage R, Zaller JG (eds) Herbicides: Chemistry, efficacy, toxicology, and environmental impacts. Emerging issues in analytical chemistry. Elsevier, Amsterdam, pp 231–272
Brühl CA, Zaller JG (2019) Biodiversity decline as a consequence of an inappropriate environmental risk assessment of pesticides. Front Environ Sci 7:177. https://doi.org/10.3389/fenvs.2019.00177
Acknowledgements
We are grateful for the comments of four anonymous reviewers who helped to improve the manuscript. Our thanks also go to Angeliki Lysimachou for discussions on EU pesticide legislation. SzK and ASz are fellows of the Research Excellence Program, Hungarian University of Agriculture and Life Sciences.
Funding
Open access funding provided by University of Natural Resources and Life Sciences Vienna (BOKU). This work was supported by Erasmus + project Hort4EUGreen (2020-1-RO01-KA203-080398).
Author information
Authors and Affiliations
Contributions
SzK: conceptualization; writing—original draft; review and editing. GS: conceptualization; writing—original draft. MO: writing—original draft. ET: writing—original draft. RM: supervision; writing—review and editing. MNA: supervision; writing—review and editing. JGZ: supervision; writing—review and editing. ASz: supervision; writing—review and editing. All authors read and approved the final manuscript.
Corresponding authors
Ethics declarations
Ethics approval and consent to participate
Not applicable.
Consent for publication
Not applicable.
Competing interests
R.M. has served as a consultant on glyphosate risk assessment issues as part of litigation in the United States over glyphosate health effects. The other authors declare that they have no competing interests.
Additional information
Publisher's Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
About this article
Cite this article
Klátyik, S., Simon, G., Oláh, M. et al. Aquatic ecotoxicity of glyphosate, its formulations, and co-formulants: evidence from 2010 to 2023. Environ Sci Eur 36, 22 (2024). https://doi.org/10.1186/s12302-024-00849-1
Received:
Accepted:
Published:
DOI: https://doi.org/10.1186/s12302-024-00849-1