Pre-harvest retting of flax: effects of water stress on uptake and efficacy of glyphosate

The effects of water stress on the uptake, translocation and efficacy of glyphosate in flax were investigated in relation to pre-harvest retting. Glyphosate (applied at a rate equivalent to 1.44 kg a.e. ha^-1 at 0, 10, 20 or 30 days after the start of flowering) caused little desiccation of flax grown in pots under restricted watering. Glyphosate application to well-watered plants caused the moisture content to decline from an initial value of 70 – 80% to approximately 40% at 3 wk after spraying. Glyphosate was applied 2 wk after the mid-point of flowering to flax grown in soil with moisture contents of 35, 31, 26, 22, 16 or 12%. Soil moisture levels (16% and 12%) which restricted evapotranspiration also reduced the efficacy of glyphosate but did not affect uptake of ¹⁴C-glyphosate. Translocation of ¹⁴C-glyphosate out of treated leaves was reduced only in the most severely stressed plants (12% soil moisture). Experiments with young plants (4 wk old) confirmed that water stress slightly reduced downward translocation of glyphosate. When the herbicide was applied to young plants under conditions which minimised differences in translocation, 10.8 μg glyphosate was sufficient to desiccate unstressed plants but 108 μg had little effect on stressed plants. This indicates that, in addition to any reduction in translocation which occurs during drought, water stress may reduce the susceptibility of flax to glyphosate. Thus only relief of plant water stress by irrigation is likely to improve response of the flax crop to glyphosate.     

Investigating the mechanisms of glyphosate resistance in <Emphasis Type="Italic">Lolium multiflorum</Emphasis>

Evolved resistance to the herbicide glyphosate has been reported in eleven weed species, including Lolium multiflorum. Two glyphosate-resistant L. multiflorum populations were collected, one from Chile (SF) and one from Oregon, USA (OR), and the mechanisms conferring glyphosate resistance were studied. Based on a Petri dish dose–response bioassay, the OR and the SF populations were two and fivefold more resistant to glyphosate when compared to the susceptible (S) population, respectively; however, based on a whole-plant dose–response bioassay, both OR and SF populations were fivefold more resistant to glyphosate than the S population, implying that different resistance mechanisms might be involved. The S population accumulated two and three times more shikimic acid in leaf tissue 96 h after glyphosate application than the resistant OR and SF populations, respectively. There were no differences between the S and the glyphosate-resistant OR and SF populations in ¹⁴C-glyphosate leaf uptake; however, the patterns of ¹⁴C-glyphosate translocation were significantly different. In the OR population, a greater percentage of ¹⁴C-glyphosate absorbed by the plant moved distal to the treated section and accumulated in the tip of the treated leaf. In contrast, in the S and in the SF populations, a greater percentage of ¹⁴C-glyphosate moved to non-treated leaves and the stem. cDNA sequence analysis of the EPSP synthase gene indicated that the glyphosate-resistant SF population has a proline 106 to serine amino acid substitution. Here, we report that glyphosate resistance in L. multiflorum is conferred by two different mechanisms, limited translocation (nontarget site-based) and mutation of the EPSP synthase gene (target site-based).     

Causes of uneven desiccation of flax by glyphosate: poor penetration of the canopy and variable spray deposition

Flax (Linum usitatissimum) cv. Hera was grown at densities of c. 2000, 1500 and 1000 plants m^-2sprayed with glyphosate (1·44 kg a.e. ha^-1) and red dye (1·5%). Dye deposition was measured and the mean total was 402 , 503 and 602 μg per plant or 691, 761 and 761 μg g^-1DW for high, intermediate and low densities respectively. Variation between plants was large and significant differences were found only in deposition on the lower stem, this being about two-fold higher for plants grown at 1000 m^-2than 2000 m^-2. However spray penetration through the crop canopy was poor and only c. 4% of the total deposit was intercepted by the lower stem. There was no detectable dye deposition on the lower stem of some plants in stands of all densities. The minimum deposits of glyphosate required for desiccation were assessed by applying precise doses, using a microsyringe, to plants grown under controlled environmental conditions. A total dose of 40 μg applied to the capsules, the upper stem plus leaves and the lower stem in the approximate ratio found for dye deposition on field grown plants, was required for successful desiccation. The minimum amount of glyphosate deposited in the field experiment, calculated assuming a linear relationship between dye and glyphosate deposition, was only 5 μg per plant. Position of application was also important. Application of 6 μg glyphosate to the lower stem caused desiccation of the whole plant whereas in applications to the upper stem and leaves 64 μg was required to have a similar effect. These experiments indicate that uneven desiccation of flax crops can be accounted for by both lack of uniformity of spray deposition and poor penetration of spray through the canopy to the lower stem, where glyphosate would be most active.     

Glyphosate tolerance by Clitoria ternatea and Neonotonia wightii plants involves differential absorption and translocation of the herbicide

Glyphosate tolerance by Clitoria ternatea, Neonotonia wightii and Amaranthus hybridus was studied in whole plants from Mexico. Experiments in a controlled growth chamber showed both legumes to be highly tolerant of glyphosate, with and ED₅₀ values of 600.18 g ae ha^?C1 for C. ternatea and 362.94 g ae ha^?C1 for N. wightii. On the other hand, A. hybridus was highly susceptible to the herbicide (ED₅₀?=?42.22 g ae ha^?C1). Shikimate accumulation peaked 96 h after treatment in the tolerant plants and the susceptible weed under 500 g ae ha^?C1 glyphosate. The shikimic acid content of whole leaves was 4.0 and 5.0 times higher in the susceptible weed than in N. wightii and C. ternatea, respectively. ¹⁴C-glyphosate absorption and translocation tests showed A. hybridus to absorb 30% more herbicide than the legumes 24 h after glyphosate foliar application. ¹⁴C-glyphosate translocation as measured by quantified autoradiography revealed increased translocation of the herbicide to untreated leaves and roots in A. hybridus relative to the two legumes. The cuticular surface of A. hybridus exhibited very low wax coverage relative to the epicuticular surface of N. wightii and, especially, C. ternatea. No significant degradation of glyphosate to aminomethylphosphonic acid and glyoxylate metabolites was detected among the tolerant leguminous plants or the susceptible weed population. These results indicate that the high glyphosate tolerance of Clitoria ternatea and Neonotonia wightii is mainly a result of poor penetration and translocation of the herbicide to apical growing points in their plants.     

Effects of glyphosate on the movement of assimilates of two Lolium perenne L. populations with differential herbicide sensitivity

Glyphosate applications trigger the depletion of aromatic amino acid pools and the decrease of photosynthesis that results in changes in carbon metabolism. The aim of this work was to determine the effect of glyphosate on the export of ¹⁴C from ¹⁴C-glucose to the main sinks, by comparing a glyphosate-resistant Lolium perenne population with a susceptible one. Untreated plants of the two populations grown in hydroponics were labeled with ¹⁴C-glucose applied at the youngest expanded leaf at the tillering stage. Similar ¹⁴C-glucose absorption and ¹⁴C distribution patterns were recorded in both populations. In another experiment, half of the plants of each population were treated with glyphosate, whereas the other half was sprayed with water (controls). Glucose absorption did not vary under glyphosate treatment, regardless of the sensitivity of each population to the herbicide. However, the translocation of ¹⁴C and its distribution patterns were significantly affected by glyphosate within 1 day in the susceptible population. The treated susceptible plants showed 57% higher ¹⁴C retention at the labeled area than their controls. The lower ¹⁴C movement significantly affected the unexpanded leaves and the apical meristem on the labeled tiller. Moreover, the ¹⁴C released from roots was significantly decreased by glyphosate only in the susceptible plants. Glyphosate did not influence leaf absorption, translocation, or release of ¹⁴C-labeled glucose plus radiolabeled metabolites in the resistant population.     

Modification of root bud growth in Canada thistle with selected plant growth regulators: effects on translocation of glyphosate

Root applications of 0.1 M 6-benzyladenine (BA) and 10.0 M indole-3-butyric acid (IBA) enhanced or inhibited, respectively, root bud growth in hydroponically grown Canada thistle [Cirsium arvense (L.) Scop.]. Translocation of¹⁴C-glyphosate [N-(phosphonomethyl)glycine] into roots was positively correlated with this growth. Foliar applications of ethephon or chlorfluorenol also enhanced root bud growth, but glyphosate translocation was only weakly correlated with such growth in soil-grown Canada thistle. At glyphosate rates above 0.56 kg/ha, root bud growth was not stimulated by plant growth regulators (PGRs) and basipetal translocation was not enhanced. Paradoxically, ethephon and chlorflurenol restrained root bud growth in the field since thistle control steadily improved during the 3 years following treatment.     

Pre-harvest retting of flax: a light microscope study of the effects of glyphosate treatment on the maturation of stem tissues

A range of glyphosate treatments was applied to flax at three stages of flowering. Spraying at a rate equivalent to 1.4 kg a. e./ha at the start of flowering gave satisfactorily uniform premature desiccation and was selected for investigation of the effects of the herbicide on stem tissues, using light microscopy. During normal maturation, increase in fibre cell wall thickness, lignification of the fibres and differentiation of the secondary xylem continued for 3–5 wk after the beginning of flowering. This differentiation was halted by the application of glyphosate. Three wk after treatment various types of tissue damage were observed. In some sections epidermal and cortical cells showed the most damage, this being consistent with herbicide uptake at the stem surface. In other sections phloem and associated parenchyma cells showed the most damage. Disintegration of phloem and cortical cells occurred in some treated stem segments and caused separation of the fibre bundles from their surrounding tissues. This resembled the release of fibre bundles which results from conventional post-harvest retting. The potential of glyphosate application to flax as a pre-harvest retting technique is discussed.     

LEAF DEVELOPMENT,PHOTOSYNTHESIS, AND C14 DISTRIBUTION IN POPULUS DELTOIDES SEEDLINGS

Rates of net photosynthesis and dark respiration and distribution of C¹⁴ from selected leaves were determined for young cottonwood (Populus deltoides) trees at different stages of development. Four series of five trees—one series for each of four treated leaf positions—were included in the study. Maximum C¹⁴ export occurred when a leaf had just attained maximum size. Lower stem leaves reached maturity quickly and began exporting photosynthate when demands of the young seedling were high. Leaves at higher stem positions matured more slowly, but senescence was also delayed so their effective export life was prolonged. Translocation from a newly exporting leaf was primarily upward to developing leaves and the apex. As a leaf at any one position aged, the translocation pattern gradually shifted from upward to bi-directional and finally to a predominantly downward direction. Photosynthate translocated downward was incorporated into stem wood and roots. Maximum photosynthetic efficiency coincided with the downward shift of C¹⁴ export. Thereafter, net photosynthesis began to decline, at first slowly and then more rapidly. The patterns of photosynthesis, respiration, and C¹⁴ export associated with leaf age all varied according to leaf position on the stem.     

The absorption, translocation and distribution of the herbicide glyphosate in maize expressing the CP-4 transgene

Maize (Zea mays L. var. Bonnie) transformed with a gene encoding a 5-enolpyruvylshikimate 3-phosphate synthase with altered sensitivity showed over 100-fold greater resistance to the herbicide glyphosate (N-[phosphonomethyl]glycine) in comparison with its non-transformed progenitor (parental control) at the third-leaf stage. Studies with [¹⁴C]-glyphosate at a dosage lethal to the parental control, but sublethal to the transgenic, revealed that a maximum of 45-65% of the applied dose was absorbed, with greater absorption occurring in transgenic plants. Translocation of glyphosate was closely related to its absorption (r value 0.956) with approximately 15% more of the applied dose being mobilized in transgenic plants than the parental controls. Analysis of electronic autoradiograms along the treated leaf lamina found discrete internal regions of glyphosate accumulation closely associated with the site of application. These regions contained lower amounts of glyphosate present in the treated leaf lamina was almost completely translocated in transgenic plants, while in the parental controls more remained and the leaf became necrotic. In both types of maize there was a small accumulation of herbicide in the tip region of the leaf which was not mobilized. Younger shoot tissues and roots were major sinks for translocated glyphosate accumulating approximately 25-40% of the applied dose depending upon treatment. In the parental control, equal amounts of glyphosate were found distributed between young shoot tissues and roots; while in transgenic plants, the young shoot tissue accumulated around three times more glyphosate than the roots. In both plant types, glyphosate was localized in the meristems and young, actively growing leaves. Specific glyphosate activity (the amount of glyphosate per unit dry weight of tissue) in the major sinks of the transgenic declined towards the end of the treatment period but remained relatively constant in the parental control. In conclusion, enhancing glyphosate resistance by genetic transformation influenced the absorption, translocation and distribution of this herbicide in whole plants.Keywords: Zea mays, glyphosate (N-[phosphonomethyl]-glycine), transgenic, absorption, translocation, source-sink.      

Distinct non-target site mechanisms endow resistance to glyphosate,ACCase and ALS-inhibiting herbicides in multiple herbicide-resistant <Emphasis Type="Italic">Lolium rigidum</Emphasis>

This study investigates mechanisms of multiple resistance to glyphosate, acetyl-coenzyme A carboxylase (ACCase) and acetolactate synthase (ALS)-inhibiting herbicides in two Lolium rigidum populations from Australia. When treated with glyphosate, susceptible (S) plants accumulated 4- to 6-fold more shikimic acid than resistant (R) plants. The resistant plants did not have the known glyphosate resistance endowing mutation of 5-enolpyruvylshikimate-3 phosphate synthase (EPSPS) at Pro-106, nor was there over-expression of EPSPS in either of the R populations. However, [¹⁴C]-glyphosate translocation experiments showed that the R plants in both populations have altered glyphosate translocation patterns compared to the S plants. The R plants showed much less glyphosate translocation to untreated young leaves, but more to the treated leaf tip, than did the S plants. Sequencing of the carboxyl transferase domain of the plastidic ACCase gene revealed no resistance endowing amino acid substitutions in the two R populations, and the ALS in vitro inhibition assay demonstrated herbicide-sensitive ALS in the ALS R population (WALR70). By using the cytochrome P450 inhibitor malathion and amitrole with ALS and ACCase herbicides, respectively, we showed that malathion reverses chlorsulfuron resistance and amitrole reverses diclofop resistance in the R population examined. Therefore, we conclude that multiple glyphosate, ACCase and ALS herbicide resistance in the two R populations is due to the presence of distinct non-target site based resistance mechanisms for each herbicide. Glyphosate resistance is due to reduced rates of glyphosate translocation, and resistance to ACCase and ALS herbicides is likely due to enhanced herbicide metabolism involving different cytochrome P450 enzymes.     

Apoplastic and symplastic pathways of atrazine and glyphosate transport in shoots of seedling sunflower

[¹⁴C]Atrazine (2-chloro-4-[ethylamino]-6-[isopropylamino]-s-triazine) and [¹⁴C]glyphosate (N-[phosphonomethyl]glycine) were xylem fed to sunflower shoots at 100 micromolar for 1 hour in the light, then placed in the dark at 100% relative humidity for 1, 4, 7, or 10 hours. The distribution of atrazine and glyphosate between shoot parts, in the leaves, and between the aoplast and symplast of the leaf was determined. The apoplastic concentrations and distribution patterns of atrazine and glyphosate in the leaves were evaluated using a pressure dehydration technique, our results were compared to the previously reported distribution patterns of the naturally occurring apoplastic leaf solutes, and the apoplastic dye PTS (trisodium 3-hydroxy-5,8,10-pyrenetrisulfonate). The pattern of atrazine and glyphosate distribution in the shoot, and between the leaf apoplast and symplast, was found to reflect the potential of these herbicides to enter the shoot symplast. The results of this study are discussed with respect to current theories of xenobiotic transport in plants, and have been found to be consistent with the intermediate permeability hypothesis for xenobiotic transport.     

Morphological responses of different eucalypt clones submitted to glyphosate drift

This work aimed to evaluate the effects of simulated glyphosate drift on leaf growth and micromorphology of Eucalyptus spp. clones, using subdoses. A factorial scheme consisting of three clones, Eucalyptus urophylla, E. grandis and the hybrid E. urophylla × E. grandis (E. urograndis) and five sub-rates (0; 43.2; 86.4; 172.8 and 345.6 g e.a. ha⁻¹ of glyphosate) were used in a randomized block design, with four repetitions. The herbicide was applied on the plants so as not to reach the superior third, 23 days after seedling planting. At 7 and 15 days after application (DAA), the leaves collected from the first basal branch of the plants were processed according to the conventional methodology used for micromorphological studies. The effects of glyphosate drift were proportional to the rates tested, with E. urophylla being more tolerant to the herbicide than E. grandis and E. urograndis. Glyphosate symptoms were the same for the different clones tested, being characterized by wilting, chlorosis and leaf curling, and, at higher rates, by necrosis, foliar senescence and death of the eucalypt plants. Plants submitted to 172.8 and 345.6 g ha⁻¹ of glyphosate had severe injuries in the aerial part, affecting their development, resulting in reduced height, stem diameter and dry mass at 50 DAA. The micromorphological damages occurred prior to the appearance of visible symptoms, with erosion of the epicuticular waxes and fungal hypha infestation in plants exposed to glyphosate drift being observed in the three clones. No marked difference in leaf micromorphology was observed that could explain the differential tolerance among the three clones studied. The results show that further studies on wax and cuticle constitution of Eucalyptus spp. are needed for the elucidation of the mechanisms of differential tolerance of eucalypt species and clones to glyphosate.     

Translocation of Shoot-Applied Indolylacetic Acid into the Roots of Populus tremula

Application of 10 to 100 μg indol-3-ylacetic acid to the leaves of rooted cuttings of aspen caused inhibition of root growth after three hours. Root growth recovered within 24 hours after IAA treatment. Swelling of the root tips occurred during the period of inhibition. The roots responded in the same way if IAA was applied in solution to the cut stem surface above the mature leaves. IAA-1-¹⁴C applied through a cut stem surface or to mature leaves was translocated downwards in the plants and labelled IAA could be isolated from the roots 3 to 24 hours after application. The ethanol-soluble activity decreased rapidly indicating a rapid metabolism or binding of IAA. IAA-1-¹⁴C applied to growing leaves was not translocated. From the rapid response of root growth it was concluded that IAA was translocated into the roots at a rate of about 7 cm per hour. This rate of translocation indicates that the sieve tubes are involved in the translocation. Implications of the results for the translocation of endogenous auxin into the roots are discussed.     

Translocation of sitosterol and related compounds in Pelargonium hortorum and helianthus annuus

The translocation of several plant sterols and a triterpene was studied in geranium and sunflower plants. Upward translocation of sitosterol-[¹⁴C] and β-amyrin-[¹⁴C] was shown within 48 hr to the upper parts of a geranium plant sectioned previously above the roots. Downward translocation of sitosterol-[¹⁴C] from the leaf of application was evident in intact plants after 48 hr. In addition to free sitosterol-[¹⁴C] considerable amounts of sitosteryl-[¹⁴C] glycoside and traces of sitosteryl-[^14C] ester were found in most parts examined. Very slow downward translocation of cholesterol-[¹⁴C] but not of desmosterol-[¹⁴C], sitosteryl-[¹⁴C] palmitate or β-amyrin-[¹⁴C] was shown in geranium. In sunflower no downward translocation of cholesterol-[³H], sitosteryl-[³H] acetate or palmitate could be detected. In geranium, sitosteryl-[¹⁴C] glycoside translocated downward from the leaf of application to all other plant parts, except other leaves, and was found in these parts after 10 days as the unchanged glycoside, free sterol and steryl ester. The effect of drying the plant parts on the recovery of radioactive steroidal material is discussed. Traces of a water soluble, dialyzable form of sterol-[¹⁴C] were also detected in dried geranium roots after treatment with strong acid or alkali.     

Glyphosate resistance in a Chilean Lolium multiflorum

Lolium multiflorum (Italian ryegrass) has recently demonstrated itself to be poorly controlled with glyphosate in cereal crops of South Chile. The concentration of glyphosate necessary to reduce shoot length by 50% (ED50) in seedlings, after eight days of root contact was 7.3-fold in the resistant Vil-1 than in the susceptible (S) biotype. The obtained spray retention values were higher on S than the resistant (Vil-1) biotype. Contact angles measured on the adaxial surface of S and Vil-1 were similar. However, on the abaxial surface contact angles were of 63 degrees on Vil-1 as compared to 42 degrees on S. A greater glyphosate uptake was observed through the abaxial surface of S. Regarding translocation, glyphosate accumulated mainly in the tip of the treated leaf of Vil-1, 24 h after treatment. It was afterwards also well distributed to the rest of the leaves and roots, as in the susceptible biotype. Nevertheless, 14C-glyphosate remained higher in the foliar apex of Vil-1. Hence, resistance to glyphosate by the Vil-1 Lolium multflorum biotype seems to involve a lower uptake through the abaxial leaf surface and a different migration pattern.     

14C Translocation pathways in honeylocust and green ash: Woody plants with complex leaf forms

Long-distance transport in plants requires precise knowledge of vascular pathways, and these pathways differ among species. This study examines the ¹⁴C translocation pathways in honeylocust (Gleditsia triacanthos L.) and green ash (Fraxinus pennsylvanica Marsh.), species with compound leaves, and compares them with those of cottonwood (Populus deltoides Bartr. ex Marsh.), a species with simple leaves. The stem vasculature of honeylocust conforms to a 2/5 helical phyllotaxy and that of green ash to a decussate phyllotaxy. The plastochron is relatively long in both species – 2.5+ days in honeylocust and 4.5+ days in green ash. Consequently, the transition from upward to downward translocation from mature source leaves is abrupt and occurs close to the apex. Export of ¹⁴C from localized treatment positions within a leaf was found to vary both quantitatively and spatially. To determine export patterns, ¹⁴CO₂ was administered to either individual leaflets of once-pinnate or pinnae of bipinnate leaves of honeylocust, and to either individual veins of simple or leaflets of compound leaves of green ash. Transections of either the petiole or rachis base were then examined for ¹⁴C by micro-autoradiography. In all cases, as treatment positions advanced acropetally in the leaves, the bundles translocating ¹⁴C were situated more dorsally in the basal petiole and rachis vasculatures. ¹⁴C was confined to the right side of the vasculature when structures on the right side of a leaf were treated. Compound leaves of both species mature acropetally. Thus, mature basal pinnae of honeylocust and basal leaflets of green ash translocate acropetally to younger leaf parts that are still rapidly expanding. All translocation pathways, both in the stem and leaf, conformed with vascular organization previously determined by anatomical analyses.     

14CO2 Assimilation and 14C-photosynthate Translocation in Different Leaves of Sunflower

Chlorophyll and nitrogen contents were highest in leaves of middle position, similarly as photosynthetic efficiency represented by ¹⁴C fixation (maxima in leaf 5 from the top). All the leaves lost ¹⁴C after 2 weeks of ¹⁴CO₂ exposure. However, the reduction in radioactivity was less in young upper leaves than in the mature lower leaves. Leaves exported ¹⁴C-photosynthates to stem both above and below the exposed leaf. Very little radioactivity was recovered from the seeds of plants in which only first or second leaves were exposed to ¹⁴CO₂ implying thereby that the carbon contribution of first two leaves to seed filling was negligible. The contribution of leaves to seed filling increased with the leaf position up to the sixth leaf from the top and after the seventh leaf their contribution to seed filling declined gradually.     

Absorption and efflux of glyphosate by cell suspensions

The absorption and efflux of [¹⁴C]-glyphosate (N-[phosphonomethyl]glycine) was studied in maize (Zea mays L. cv. Aussie) and soybean (Glycine max L. Merr. cv. Maple Arrow) cell suspensions. Glyphosate absorption was complex: at low external herbicide concentrations (3-250 M) there was evidence for a single active uptake system with an apparent Km of 31 M and Vmax of 11 nmol g^-1 fr. wt. 2 h^-1. The system was inhibited by carbonylcyanide m-chlorophenyl hydrazone (CCCP), orthovanadate, diethylstilbestrol (DES), phosphate, and phosphonoformic acid (PFA) suggesting the glyphosate carrier to be a phosphate transporter energized by the plant plasmalemma ATPase. At higher external glyphosate concentrations the operation of this carrier was masked as passive diffusion became the dominant absorption mechanism. Any non-specific binding of glyphosate to the cell surface during absorption was low (0.02-0.02 nmol g^-1 fr. wt). Efflux kinetics of [¹⁴C]-glyphosate suggests the herbicide to be located in the cells in three kinetically distinct compartments: after 24 h uptake of radiolabelled herbicide, 71% of absorbed glyphosate was found in the slow compartment (t1/2 162 h), 19% in the medium (t1/2 185 min) and 10% in the fast (t1/2 27 min). The implications of these results in relation to the delivery of glyphosate to its subcellular target site and subsequent phytotoxicity are discussed.Keywords: Zea mays, Glycine max, glyphosate (N-[phosphonomethyl]glycine), absorption, compartmentation.      

Release of lateral buds from apical dominance by glyphosate in soybean and pea seedlings

Application of a sublethal dose of glyphosate (N-[phosphonomethyl]glycine) to the seedlings of soybean (Glycine max L. Merr. cv. Evans) and pea (Pisum sativum L. cv. Alaska) promoted growth of the cotyledonary and other lateral buds. The pattern of the glyphosate-induced lateral bud growth was different from that induced by decapitation. Under the experimental condition, glyphosate did not kill the apical buds. Feeding stem sections of the seedlings with radiolabeled indole-3-acetic acid ([2¹⁴C]IAA) and subsequent analysis of free [2-¹⁴C]IAA and metabolite fractions revealed that the glyphosate-treated plants had higher rates of IAA metabolism than the control plants. The treated pea plants metabolized 75% of [2-¹⁴C]IAA taken up in the 4-h incubation period compared to 46.5% for the control, an increase of 61%. The increase was small but consistent in soybean seedlings. As a result, the glyphosate-treated plants had less free IAA and ethylene than the control plants. The increase of IAA metabolism induced by glyphosate is likely to change the auxin-cytokinin balance and contribute to the release of lateral buds from apical dominance in these plants.     

Release of lateral buds from apical dominance by glyphosate in soybean and pea seedlings

Application of a sublethal dose of glyphosate (N-[phosphonomethyl]glycine) to the seedlings of soybean (Glycine max L. Merr. cv. Evans) and pea (Pisum sativum L. cv. Alaska) promoted growth of the cotyledonary and other lateral buds. The pattern of the glyphosate-induced lateral bud growth was different from that induced by decapitation. Under the experimental condition, glyphosate did not kill the apical buds. Feeding stem sections of the seedlings with radiolabeled indole-3-acetic acid ([2¹⁴C]IAA) and subsequent analysis of free [2-¹⁴C]IAA and metabolite fractions revealed that the glyphosate-treated plants had higher rates of IAA metabolism than the control plants. The treated pea plants metabolized 75% of [2-¹⁴C]IAA taken up in the 4-h incubation period compared to 46.5% for the control, an increase of 61%. The increase was small but consistent in soybean seedlings. As a result, the glyphosate-treated plants had less free IAA and ethylene than the control plants. The increase of IAA metabolism induced by glyphosate is likely to change the auxin-cytokinin balance and contribute to the release of lateral buds from apical dominance in these plants.