Characteristics and control of dicamba‐resistant common lambsquarters (Chenopodium album)

The expansion of atrazine‐resistant Chenopodium album (common lambsquarters) since the 1980s has forced New Zealand's maize‐growers to use an additional postemergence herbicide application. The frequent use of dicamba for this has selected for a common lambsquarters population with reduced sensitivity to dicamba. Initial greenhouse experiments with seeds that had been collected from the plants that survived field applications of dicamba showed that these plants could tolerate ≤1.2 kg ha^?1, fourfold the recommended rate. These dicamba‐resistant plants were morphologically distinct from the susceptible population. The leaves of the resistant plants were less dentate and a lighter shade of green. The resistant plants were shorter, had a lower biomass and growth rate and flowered ≤19 days earlier than the susceptible plants. When grown together in various density ratios, the average biomass of both the susceptible and the resistant plants increased as the number of susceptible plants decreased in the mixture. The field experiments demonstrated that the resistant population tolerated dicamba at ≤2.4 kg ha^?1, eightfold the recommended rate. Postemergence applications of bromoxynil, pyridate, nicosulfuron and mesotrione effectively controlled both populations. Nicosulfuron and mesotrione provided long‐term residual control, with nicosulfuron being more effective on the grass weeds. High rates of dicamba damaged the maize plants, resulting in an increased weed cover and reduced grain yield. The number of viable common lambsquarters seeds in the soil seed bank at the end of the growing season declined in the treatments in which common lambsquarters was controlled effectively.     

Seed germination and viability of herbicide resistant and susceptible Chenopodium album populations after ensiling,digestion by cattle and manure storage

Chenopodium album became a problem weed in sugar beet production, due to resistance to metamitron, a key herbicide in this crop. Dispersal of the seeds from resistant biotypes may occur due to spread by wind, animals, agricultural machinery or manure. This study examined the effect of ensiling, digestion by cattle and storage in slurry and farmyard manure on the germination and viability of the seeds of one susceptible and three resistant C. album populations. After 4 weeks in a maize silo, seed viability of C. album populations was reduced drastically to 0–5%. Incubation for 24 h in the rumen followed by a post‐ruminal digestion in vitro of intact seeds only resulted in a small reduction in viability in one C. album population. Storage in a slurry cellar for 16 weeks reduced the viability of intact seeds of the C. album populations to 25–60%. Only 0–1% of the seeds remained viable after storage in a farmyard manure heap for 4 weeks. An accelerated ageing experiment showed seed persistence to be population specific and less related to seed weight. Keeping a fresh maize silo closed for at least 4 weeks and heaping farmyard manure are excellent preventive measures to limit the spread of resistant C. album seeds between fields.     

A new molecular method for the rapid detection of a metamitron‐resistant target site in Chenopodium album

BACKGROUND: Resistance to photosystem II inhibitors—triazines (atrazine) and triazinones (metamitron, metribuzin)—in Chenopodium album L. is caused by the serine 264 to glycine mutation in the D1 protein. This mutation has been detected in C. album collections from Belgium with unsatisfactory metamitron efficacy in the field and was confirmed in greenhouse resistance bioassays. Incomplete herbicide efficacy in practice can also be caused by reduced uptake due to environmental conditions. Hence, for reliable differentiation and resistance identification, a rapid method for mutation detection in the target gene psbA is required. RESULTS: Dose–response curves obtained in herbicide greenhouse assays with metamitron‐resistant and ‐susceptible reference biotypes showed that a dose of 2 L ha^?1 metamitron was suitable for discrimination. A psbA PCR‐RFLP was developed, based on the presence of a FspBI restriction enzyme recognition site, covering D1 codon 264 in susceptible genotypes. A paper‐based DNA extraction allowed direct processing of leaf samples already in the field. In order to detect the mutation even in mixed seed samples, a nested PCR‐RFLP was also developed. CONCLUSION: The method allows exhaustive surveys screening C. album leaf or seed samples for the occurrence of the D1 Ser264Gly mutation to confirm or disprove metamitron resistance in the case of unsatisfactory control. Copyright © 2010 Society of Chemical Industry     

Absorption,translocation and metabolism of aminocyclopyrachlor in young plants of Ipomoea purpurea and Ipomoea triloba

Members of the Convolvulaceae family are known to be sensitive to aminocyclopyrachlor, although little is known about the absorption, translocation and metabolism of the herbicide in these species of weed. The aim of this study was to evaluate the absorption, translocation and metabolism of ¹⁴C‐aminocyclopyrachlor in young plants of Ipomoea purpurea and Ipomoea triloba. Assessments were performed at 3, 6, 12, 24, 48 and 72 h after treatment (HAT) for the study of absorption and translocation. Metabolism was assessed at three time points (3, 24 and 72 HAT). In terms of absorption, was observed a difference between species at the 3 and 48 HAT time points, where I. purpurea had a higher absorption of ¹⁴C‐aminocyclopyrachlor. No differences were observed between species at any other time points. Of the total absorbed herbicide, 90.9% for I. purpurea and 91.8% for I. triloba were detected on the treated leaf. I. purpurea presented higher translocation to the leaf above the treated leaf, while I. triloba showed higher translocation to the lower leaves and roots. No increase in absorption of ¹⁴C‐aminocyclopyrachlor was observed above 24 HAT for I. purpurea and above 6 HAT for I. triloba, and translocation was low (<1%) for both species in all plant parts. This suggests that post‐emergence application of aminocyclopyrachlor cannot be effective for the control of I. purpurea and I. triloba and alternative approaches are required. Nevertheless, no ¹⁴C‐aminocyclopyrachlor metabolites were observed in the studied plants, which indicated sensitivity in I. purpurea and I. triloba to the herbicide.     

Fate of the herbicides glyphosate, glufosinate-ammonium, phenmedipham, ethofumesate and metamitron in two Finnish arable soils

The fate of five herbicides (glyphosate, glufosinate-ammonium, phenmedipham, ethofumesate and metamitron) was studied in two Finnish sugar beet fields for 26 months. Soil types were sandy loam and clay. Two different herbicide-tolerant sugar beet cultivars and three different herbicide application schedules were used. Meteorological data were collected throughout the study and soil properties were thoroughly analysed. An extensive data set of herbicide residue concentrations in soil was collected. Five different soil depths were sampled. The study was carried out using common Finnish agricultural practices and represents typical sugar beet cultivation conditions in Finland. The overall observed order of persistence was ethofumesate > glyphosate > phenmedipham > metamitron > glufosinate-ammonium. Only ethofumesate and glyphosate persisted until the subsequent spring. Seasonal variation in herbicide dissipation was very high and dissipation ceased almost completely during winter. During the 2 year experiment no indication of potential groundwater pollution risk was obtained, but herbicides may cause surface water pollution.     

Morphophysiological traits and atrazine sensitivity in Chenopodium album L

BACKGROUND: A Chenopodium album L. biotype surviving in atrazine-treated Serbian corn fields (VC) was compared against atrazine-susceptible (S) and atrazine-resistant (R) standards.RESULTS: Atrazine (2 kg ha(-1)) killed S and VC shoot biomass 15 days after treatment (DAT), but R was only suppressed by 42% and survived 8 kg ha(-1). Atrazine at 2 kg ha(-1) only inhibited VC height by 60% as against 100 and 0% for S and R respectively. Chlorophyll fluorescence (Fv/Fm) and transpiration were insensitive to atrazine in R, but were inhibited by 90 and 100% in S and by 50 and 60% in VC respectively. Decline of Fv/Fm after 2 kg ha(-1) atrazine was stabilized at 3 DAT for the VC biotype.CONCLUSION: A toxicity mitigation mechanism could have facilitated VC survival in an atrazine-treated field. Further knowledge on this mechanism is needed to establish if surviving VC plants are indicators of atrazine resistance evolution in these Serbian corn fields. Variables related to foliar function provided better detection of weed mechanisms to survive herbicide action than the usual shoot biomass measurements.     

Absorption, translocation and metabolism of pyridate in a tolerant crop (Zea mays) and two susceptible weeds (Polygonum lapathifolium L. and Chenopodium album L.)

Absorption, translocation and metabolism of ¹⁴C-pyridate were compared in tolerant maize. moderately susceptible Polygonum lapathifolium and susceptible Chenopodium album. Foliar absorption was limited in all species, but comparatively higher penetration levels were observed in younger leaves of dicotyledonous species. The absorbed radioactivity was not very mobile and translocation appeared mainly sym-plastic. Herbicide selectivity could not be explained on the basis of absorption and transport. Chenopodium and P. lapathifolium degraded pyridate and formed unstable water-soluble conjugates that easily released a phytotoxic metabolite. By contrast, more stable unidentified water-soluble metabolites were found in maize. That metabolic difference could explain the selectivity of pyridate.     

Differential sensitivity of Atriplex patula and Chenopodium album to sugar beet herbicides: a possible cause for the upsurge of A. patula in sugar beet fields

In the last decade, the prevalence of Atriplex patula as a weed in the Belgian sugar beet area has increased. Possible reasons for its expansion in sugar beet fields, besides a poor implementation of the low‐dose phenmedipham/activator/soil‐acting herbicide (FAR) system, might be low sensitivity or evolved resistance to one or more herbicides used in sugar beet. Dose – response pot bioassays were conducted in the glasshouse to evaluate the effectiveness of five foliar‐applied sugar beet herbicides (metamitron, phenmedipham, desmedipham, ethofumesate and triallate) and three pre‐plant‐incorporated herbicides (metamitron, lenacil, dimethenamid‐P) for controlling five Belgian A. patula populations. Local metamitron‐susceptible and metamitron‐resistant populations of Chenopodium album were used as reference populations. Effective dosages and resistance indices were calculated. DNA sequence analysis of the photosystem II psbA gene was performed on putative resistant A. patula populations. Overall, A. patula exhibited large intraspecific variation in herbicide sensitivity. In general, A. patula populations were less susceptible to phenmedipham, desmedipham, ethofumesate and triallate relative to C. album populations. Two A. patula populations bear the leucine‐218 to valine mutation on the chloroplast psbA gene conferring low level to high level cross‐resistance to the photosystem II inhibitors phenmedipham, desmedipham, metamitron and lenacil. In order to avoid insufficient A. patula control and further spread, seedlings should preferentially be treated with FAR mixtures containing higher‐than‐standard doses of metamitron and phenmedipham/desmedipham and no later than the cotyledon stage.     

psbA mutation (Asn266 to Thr) in Senecio vulgaris L. confers resistance to several PS II-inhibiting herbicides

DNA sequence analysis of the psbA gene encoding the D1 protein of photosystem II (PS II), the target site of PS II-inhibiting herbicides, identified a point mutation (Asn266 to Thr) in a bromoxynil-resistant Senecio vulgaris L. population collected from peppermint fields in Oregon. Although this mutation has been previously reported in Synechocystis, this is the first report of this particular point mutation in a higher plant exhibiting resistance to PS II-inhibiting herbicides. The resistant population displayed high-level resistance to bromoxynil and terbacil (R/S ratio 10.1 and 9.3, respectively) and low-level resistance to metribuzin and hexazinone (R/S ratio 4.2 and 2.6, respectively) when compared with the susceptible population. However, the population was not resistant to the triazine herbicides atrazine and simazine or to the urea herbicide diuron. A chlorophyll fluorescence assay confirmed the resistance levels and patterns of cross-resistance of the whole-plant studies. The resistant S. vulgaris plants produced fewer seeds. Differences in cross-resistance patterns to PS II-inhibiting herbicides and the difference in fitness cost could be exploited in a weed management program.     

Absorption, translocation, and metabolism of propoxycarbazone-sodium in ALS-inhibitor resistant Bromus tectorum biotypes

Experiments were conducted to investigate the absorption, translocation, and metabolism of propoxycarbazone-sodium in acetolactate synthase-inhibitor resistant (AR and MR) and susceptible (AS and MS) Bromus tectorum biotypes. Absorption and translocation of ^l4C-propoxycarbazone-sodium were similar in all biotypes. One major and three minor metabolites were identified using reverse-phase high performance liquid chromatography. In all biotypes, 80% of the propoxycarbazone-sodium was metabolized by 72 h after treatment (HAT). However, propoxycarbazone-sodium was metabolized more rapidly in the MR biotype than in the other biotypes. The half-life of propoxycarbazone-sodium in the MR biotype was 8.9 h, which was 30, 36, and 40% shorter than in the AS, AR, and MS biotypes, respectively. When ¹⁴C-propoxycarbazone-sodium was applied with 1-aminobenzotriazole, a known cytochrome P450 inhibitor, metabolism decreased 20% 12 HAT in the MR biotype. These results indicate that resistance of the MR biotype to propoxycarbazone-sodium is due to a relatively rapid rate of propoxycarbazone-sodium metabolism compared to other B. tectorum biotypes and that cytochrome P450s may be involved in the metabolism. The fact that these populations evolved so quickly and with different resistance mechanisms is a concern as more ALS inhibitors are introduced into the production systems.     

Spray retention, foliar uptake and translocation of glufosinate and glyphosate in Ambrosia artemisiifolia

Ambrosia artemisiifolia plants exhibit stomata on both leaf surfaces and three types of trichomes: (i) small (<50 μm) spherical or ovoid, (ii) medium‐sized (50–100 μm) and (iii) long (100–200 μm) and sharp. Only the long and sharp trichomes were stained with AgNO₃, indicating the presence of hydrophilic domains. Epicuticular waxes appeared amorphous, consistent with high levels of spray retention. Glufosinate was readily taken up by A. artemisiifolia leaves, with maximum uptake of >80% of the applied label, and half maximum uptake being reached within 6 h. The foliar uptake of glyphosate was nearly complete and half of it was attained after 3 h. Glufosinate and glyphosate were ambimobile and their translocation out of the treated leaves amounted to 13–16% and 11–15% of the absorbed radioactive label respectively. Glufosinate was mainly directed to the apical developing tissues, with less amounts reaching the tissues below the treated leaves. Glyphosate was directed towards the sink tissues (apical developing tissues and roots). The sensitivity of A. artemisiifolia to glufosinate and glyphosate can be explained by high spray retention, rapid and important foliar uptake, and appreciable migration out of the parts of the plant hit by the spray.     

Absorption,translocation and metabolism of the herbicide naproanilide in tobacco

Naproanilide [2-(2-naphthyloxy)propionanilide] has a high activity against dicotyledonous weeds in rice fields, but is very safe to rice. This study was designed to clarify the absorption and translocation of radiolabelled naproanilide in tobacco plants and the metabolism in tobacco callus. The results indicated that naproanilide is translocated easily to the upper part of tobacco plants. Distribution of radioactivity in tobacco plants at the 7th day was shown to be 0.88, 0.24 and 0.03%, and at the 14th day 1.71, 1.86 and 2.32% of the total activities of [¹⁴C]naproanilide in root, stem and leaf, respectively. When compared to earlier results obtained with rice, the translocation rate in tobacco is much higher and might therefore contribute a possible mechanism of herbicidal selectivity. Metabolites including NOP [2-(2-naphthyloxy)propionic acid], NOPM [methyl 2-(2-naphthyloxy)propionate], 2-naphthol, 2,3-naphthalenediol, 2,6-naphthalenediol, 2,7-naphthalenediol and 2-hydroxy-1,4-naphthoquinone were identified in tobacco callus by co-chromatography.     

Absorption,translocation, and metabolism of ethalfluralin and trifluralin in Solanum spp

Seedlings of Solanum scabrum Mill. and Solanum ptycanthum Dun. were treated with [¹⁴C]ethalfluralin (N-ethyl-α,α,α-trifluoro-N-(methylallyl)-2,6-dinitro-p-toluidine) and [¹⁴C]trifluralin (α,α,α-trifluoro-2,6-dinitro-N,N-dipropyl-p-toluidine) supplied in nutrient solution to determine the basis for differences in response by these two species to these two herbicides. Plants of S. scabrum absorbed more [¹⁴C]ethalfluralin and [¹⁴C]trifluralin than plants of S. ptycanthum. During the first 24 h, S. scabrum seedlings, but not S. ptycanthum seedlings absorbed more [¹⁴C]ethalfluralin than did plants treated with [¹⁴C]trifluralin. More [¹⁴C]ethalfluralin than [¹⁴C]trifluralin was found in the shoots of plants of both species. Seventy-two hours after treatment with [¹⁴C]herbicides, the conversion to water-soluble metabolites was greater for [¹⁴C]ethalfluralin than for [¹⁴C]trifluralin. In the shoots of plants from both species an average of nearly 55% of the ¹⁴C recovered was found in the water-soluble fraction following [¹⁴C]ethalfluralin treatment whereas an average of only 40% was found in the water-soluble fraction following [¹⁴C]trifluralin treatment.     

Reduced translocation is involved in resistance to glyphosate and paraquat in Conyza bonariensis and Conyza canadensis from California

Resistance to glyphosate and paraquat has evolved in some populations of Conyza spp. from California, USA. This study evaluated whether herbicide absorption and translocation were involved in the mechanism of resistance to both herbicides. Three lines of each species were used: glyphosate‐paraquat‐susceptible (GPS), glyphosate‐resistant (GR) and glyphosate‐paraquat‐resistant (GPR). Radiolabelled herbicide was applied to a fully expanded leaf, and absorption and movement out of the treated leaf were monitored for up to 24 h for paraquat and 72 h for glyphosate. Plants treated with paraquat were incubated in darkness for the first 16 h and then subjected to light conditions. More glyphosate was absorbed in C. bonariensis (52.9–58.3%) compared with C. canadensis (28.5–37.6%), but no differences in absorption were observed among lines within a species. However, in both species, the GR and GPR lines translocated less glyphosate out of the treated leaf when compared with their respective GPS lines. Paraquat absorption was similar among lines and across species (71.3–77.6%). Only a fraction of paraquat was translocated in the GPR lines (3% or less) when compared with their respective GPS or GR lines (20% or more) in both species. Taken together, these results indicate that reduced translocation is involved in the mechanism of resistance to glyphosate and paraquat in C. bonariensis and C. canadensis.