Barnyardgrass [Echinochloa crus-galli (L.) P. Beauv.] is increasingly infesting imidazolinone-tolerant (IMI-T) rice fields in China, imazamox resistance of E. crus-galli has become the major concern for weed management in IMI-T rice fields. In this study, the susceptible population JLGY-3 (S) and the suspected resistant population JHXY-2 (R) collected from IMI-T rice fields were used as research subjects. When treated with imazamox, JHXY-2 (R) population showed a high level of herbicide resistance with a resistance index (RI) of 31.2. JHXY-2 (R) was cross-resistant to all five acetolactate synthase (ALS) inhibitors from different chemical families, but sensitive to herbicides inhibiting acetyl-CoA carboxylase (ACCase). In order to understand the reason why JHXY-2 (R) was resistant to imazamox, we performed experiments to characterize potential TSR and NTSR mechanisms. A trp-574-leu amino acid mutation in ALS and low imazamox ALS sensitivity were the main mechanism underlying imazamox resistance in this JHXY-2 (R) population. There was no significant difference in ALS gene expression and ALS protein abundance between R and S populations. High-performance liquid chromatography-tandem mass spectrometry analysis showed enhanced metabolism of imazamox in JHXY-2 (R), which was in contrast to the results of pretreatment with a metabolic enzyme inhibitor. Treatments with the P450/GST inhibitors did not alter the resistance level of JHXY-2 (R) against imazamox. To further clarify the NTSR mechanism of JHXY-2 (R), transcriptome sequencing showed that there was almost no significant difference in the expression of P450 and GST metabolic enzyme genes between R and S populations, and only GST-U1 showed a significant induction in R population. In conclusion, amino acid mutation and higher enzyme activity of ALS are the main causes of imazamox resistance in JHXY-2 (R). However, given the differences in imazamox residues in the leaves of the E. crus-galli, there may still be undetectable NTSR that are causing imazamox resistance in the R population.

The sustainable management of herbicides is critical to modern agriculture and the environment. This article examines the evolution and environmental implications of herbicide use in Saskatchewan, Canada, agriculture. It quantifies changes in herbicide use and their environmental impacts by analyzing farm-level herbicide use data from 1991 to 1994 and from 2016 to 2019 through the environmental impact quotient. Results confirm significant reductions in both environmental and toxicological impacts of herbicides used, underlining the pivotal shift from tillage-based weed control to herbicide-resistant cropping systems. The environmental impact of the top five herbicides (glufosinate, glyphosate, clethodim, imazamox, and 2,4-D) used from 2016 to 2019 is 65% lower than that for those herbicides (MCPA, 2,4-D, bromoxynil, diclofop-methyl, and trifluralin) used from 1991 to 1994, with a 45% reduction in the active ingredient applied per acre. Despite increased herbicide use due to more crop acres being seeded, the findings highlight a marked improvement in the sustainability of herbicide use, affirming the importance of technological advancements in agriculture. This research contributes valuable insights into long-term trends in herbicide use, offering a practical framework for informed decisions aligning with sustainable agricultural practices as well as reduced biodiversity impacts.

Downy brome is a troublesome facultative winter-annual grass weed that invades agricultural and nonagricultural lands in western North America and can cause substantial crop yield losses particularly in no-till winter wheat. Glyphosate-resistant (GR) downy brome was identified in southern Alberta in 2021, representing the first confirmation of a GR grass weed in Canada. This study was designed to evaluate alternative herbicides and herbicide mixtures applied postemergence (POST) for control of GR and glyphosate-susceptible (GS) downy brome populations at the seedling stage under a controlled environment. The GR downy brome did not exhibit cross-resistance to other herbicides applied POST. Quizalofop alone or in combination with imazamox, imazamox + bentazon, or imazamox/imazethapyr, and glufosinate mixed with either clethodim or tiafenacil resulted in ≥80% visible control, plant mortality, and reduction in biomass of both GR and GS downy brome populations 21 d after treatment. Diligent stewardship of these remaining herbicide options is warranted since downy brome populations with resistance to herbicides that inhibit acetyl-CoA carboxylase or acetolactate synthase have been reported in neighboring states.

Herbicide-resistant Palmer amaranth is a troublesome weed in several agronomic crops and is a relatively new challenge to dry bean production in western Nebraska. Objectives were to evaluate preemergence (PRE) and postemergence (POST) herbicides for control of acetolactate synthase–resistant Palmer amaranth and their effect on Palmer amaranth density and biomass as well as dry bean injury and yield in western Nebraska. Field experiments were conducted in 2017 and 2019 near Scottsbluff, NE. The experiments were arranged as a two-factor strip-plot design. The strip-plot factor consisted of no-PRE or pendimethalin (1,070 g ai ha–1) + dimethenamid-P (790 g ai h–1) applied PRE. The main-plot factor was POST herbicides, which consisted of various mixtures of imazamox, bentazon, or fomesafen applied in a single or sequential application at labeled rates, and reduced rates of imazamox (9 g ai ha–1) + bentazon (314 g ai ha–1) + fomesafen (70 g ai ha–1) applied in single or sequential (two or three) applications. PRE herbicides reduced Palmer amaranth density and biomass during both years and increased dry bean yield in 2017. POST treatments containing fomesafen improved Palmer amaranth control compared with treatments containing imazamox and bentazon only. The sequential-application reduced-rate POST system did not improve Palmer amaranth control compared to one POST application containing fomesafen at a labeled rate in either year. Using pendimethalin + dimethenamid-P PRE followed by POST treatments containing imazamox + bentazon + fomesafen at a labeled rate provided 86% and 99% Palmer amaranth control in 2017 and 2019, respectively.

Rigid ryegrass is a problematic weed species in winter crops and winter fallow; however, recently, this weed species has been observed in summer crops and fallow. These observations warrant the evaluation of different postemergence herbicides for its control. Outdoor pot studies were conducted during the spring and summer of 2021 to 2022 to determine the performance of POST herbicides on two summer-emerging (S3 and S6) and two winter-emerging (W3 and W8) accessions of rigid ryegrass. Across all accessions, butroxydim, clethodim, paraquat, and paraquat + amitrole at the field rate provided complete control of rigid ryegrass. Both summer-emerging accessions were found to be resistant to the field rates of glufosinate (750 g ai ha−1), glyphosate (454 g ae ha−1), haloxyfop (52 g ai ha−1), and pinoxaden (30 g ai ha−1). The S6 accession had the highest dose required for a 50% reduction in biomass for these herbicides (glufosinate 1,120 g ai ha−1, glyphosate 1,210 g ae ha−1, haloxyfop 140 g ai ha−1, and pinoxaden 55 g ai ha−1). This summer-emerging accession (S6) was also resistant to iodosulfuron. All four accessions were found susceptible to imazamox + imazapyr (a commercial mixture) and mesosulfuron. The study provides the first evidence of poor control of summer-emerging accessions of rigid ryegrass with different herbicides. Multiple-herbicide-resistant summer-emerging rigid ryegrass accessions would be a challenge to the production of summer crops (e.g., cotton and sorghum) as well as winter crops that rely on weed-free summer fallows for soil moisture retention; therefore these accessions warrant diversified management strategies.

Biotypes of Palmer amaranth that are resistant to acetolactate synthase (ALS) inhibitor are becoming widespread in western Nebraska. There are limited effective postemergence (POST) herbicides labeled for ALS-inhibitor-resistant Palmer amaranth control in dry edible bean. The objective of this study was to evaluate the efficacy of dimethenamid-P in a sequential preemergence (PRE) fb followed by (fb) POST program at two POST application timings, the first and third trifoliate stages (V1 and V3, respectively), for controlling ALS-inhibitor-resistant Palmer amaranth in dry edible bean. A field study was conducted in 2019, 2020, and 2021 in Scottsbluff, NE. PRE-alone applications of pendimethalin + dimethenamid-P provided inconsistent Palmer amaranth control. Dimethenamid-P applied POST following a PRE application of pendimethalin + dimethenamid-P provided effective (>90%) Palmer amaranth control at 4 wk after V3 only at the V1 application timing in 2019. In 2020 and 2021 dimethenamid-P applied POST at V1 and V3 following a PRE application of pendimethalin + dimethenamid-P provided 99% and 98% Palmer amaranth control at 4 wk after V3, and 98% and 94% Palmer amaranth control at harvest, respectively. Palmer amaranth biomass was reduced by 95% to 99% and by 96% to 98% compared with the -nontreated control when dimethenamid-P was applied POST at V1 and V3, respectively, following a PRE application of pendimethalin + dimethenamid-P in 2020 and 2021. Application of a mixture of dimethenamid-P with imazamox + bentazon POST provided similar results to those of the fomesafen-containing treatments and dimethenamid-P alone POST. Dimethenamid-P applied POST following a PRE application of pendimethalin + dimethenamid-P resulted in similar yield as the fomesafen-containing treatments. If fomesafen is not an option due to the crop rotation interval restriction, using dimethenamid-P in a sequential PRE fb POST program is the only effective alternative to control ALS-inhibitor–resistant Palmer amaranth in Nebraska. The use of dimethenamid-P in a sequential PRE fb POST program, alone or mixed with foliar-active herbicides should be considered by dry edible bean growers who are dealing with ALS-inhibitor-resistant Palmer amaranth.

Late-emerging summer annual weeds are difficult to control in dry bean production fields. Dry bean is a poor competitor with weeds, due to its slow rate of growth and delayed canopy formation. Palmer amaranth is particularly difficult to control due to season-long emergence and resistance to acetolactate synthase (ALS)-inhibiting herbicides. Dry bean growers rely on PPI and preemergence residual herbicides for the foundation of their weed control programs; however, postemergence herbicides are often needed for season-long weed control. The objective of this experiment was to evaluate effect of planting date and herbicide program on late-season weed control in dry bean in western Nebraska. Field experiments were conducted in 2017 and 2018 near Scottsbluff, NE. The experiment was arranged in a split-plot design, with planting date and herbicide program as main-plot and subplot factors, respectively. Delayed planting was represented by a delay of 15 d after standard planting time. The treatments EPTC + ethalfluralin, EPTC + ethalfluralin followed by (fb) imazamox + bentazon, and pendimethalin + dimethenamid-P fb imazamox + bentazon, resulted in the lowest Palmer amaranth density at 3 wk after treatment and the highest dry bean yield. The imazamox + bentazon treatment provided poor Palmer amaranth control and did not consistently result in Palmer amaranth density and biomass reduction compared with the nontreated control. In 2018, the delayed planting treatment had reduced Palmer amaranth biomass with the pendimethalin + dimethenamid-P treatment, as compared with standard planting. Delaying planting did not reduce dry bean yield and had limited benefit in improving weed control in dry bean.

Field experiments were conducted in 2016 and 2017 to evaluate the effects of seeding rate and herbicide programs on weed control and pinto bean yield under irrigation. The experiments comprised a 5 × 5 factorial randomized complete block design with five replications. The weed control treatments comprised a nontreated control, hand-weeded control, EPTC + ethalfluralin PRE, EPTC + ethalfluralin PRE followed by (fb) dimethenamid-P POST at V1, and EPTC + ethalfluralin PRE fb bentazon/imazamox POST. There were five seeding rates ranging from 247,000 to 494,000 seeds ha–1 planted in 19-cm rows. Weed biomass was reduced by 6 kg ha–1 with every additional 1,000 seeds ha–1. EPTC plus ethalfluralin fb either dimethenamid-P or bentazon plus imazamox reduced weed biomass by at least 29% compared to the nontreated control. There was a significant effect of weed control treatment on pinto bean yield (P = 0.0004). However, there was no significant seeding rate (P = 0.42) or seeding rate–by–weed control interaction effect on pinto bean yield (P = 0.38). Pinto bean yield ranged from 3,080 kg ha–1 in the nontreated control to 4,740 kg ha–1 hand-weeded treatment. Increased seeding rate in narrow rows is a cultural practice that can improve weed control in pinto bean but may not necessarily increase yield.

Hen’s eyes (Ardisia crenata Sims) is a shade-tolerant invasive shrub displacing native understory in forests of the Coastal Plain of the southeastern United States. Few studies have explored herbicide effectiveness on A. crenata, with foliar applications of triclopyr amine or triclopyr ester typically referenced as the standard treatments. This study evaluated efficacy of eight foliar herbicide treatments and a nontreated check at three locations at 12 mo after the first treatment (12MAT1) and 12 mo after the second treatment (12MAT2) on established (greater than 8-cm high) and seedling (less than 8-cm high) A. crenata. Treatments were four triclopyr formulations: amine, ester, choline, and acid (all at 4.04 kg ae ha−1); imazamox (1.12 and 2.24 kg ae ha−1); flumioxazin (0.43 kg ai ha−1); and triclopyr amine plus flumioxazin (4.04 + 0.43 kg ae ha−1). At 12MAT1, triclopyr ester, the high rate of imazamox, and triclopyr acid resulted in greater control of established A. crenata than any other herbicide (68%, 66%, and 64%, respectively). At 12MAT2, all herbicides except flumioxazin resulted in some control of A. crenata. Triclopyr ester, triclopyr acid, and the high rate of imazamox provided 95%, 93%, and 92% control, respectively. Triclopyr choline did not perform as well as the acid or ester formulations, and the tank mix of flumioxazin and triclopyr amine did not improve control over triclopyr amine alone. This study identified triclopyr acid and imazamox (2.24 kg ae ha−1) as new options for A. crenata control and indicated variation in the performance among the four triclopyr formulations.

Field studies were conducted from 2009 through 2011 at the Sustainable Agriculture Research and Extension Center near Lingle, Wyoming, to evaluate great northern bean response to PRE flumioxazin mixed with either trifluralin, pendimethalin, or ethalfluralin. Seven treatments were arranged in a randomized complete block with three or four replicates y−1. The soil texture of the study site was loam in 2009 and 2011, and sandy loam in 2010. Soil organic matter ranged from 1.4% to 1.8%. Treatments included flumioxazin plus trifluralin, flumioxazin plus pendimethalin, flumioxazin plus ethalfluralin, ethalfluralin plus EPTC, imazamox plus bentazon (POST), hand-weeded control, and nontreated control. Dry bean density 4 wk after planting differed among herbicide treatments (P < 0.001). Treatments that included flumioxazin reduced dry bean density 54% compared with treatments without flumioxazin. Dry bean yield was influenced by dry bean density; on average, yield in flumioxazin-containing herbicide treatments was 30% less than treatments not containing flumioxazin, even though weed control was generally greater in flumioxazin treatments.

Multiple resistance to glyphosate, sethoxydim, and paraquat was previously confirmed in two Italian ryegrass [Lolium perenne L. ssp. multiflorum (Lam.) Husnot] populations, MR1 and MR2, in northern California. Preliminary greenhouse studies revealed that both populations were also resistant to imazamox and mesosulfuron, both of which are acetolactate synthase (ALS)-inhibiting herbicides. In this study, three subpopulations, MR1-A (from seed of MR1 plants that survived a 16X rate of sethoxydim), MR1-P (from seed of MR1 plants that survived a 2X rate of paraquat), and MR2 (from seed of MR2 plants that survived a 16X rate of sethoxydim), were investigated to determine the resistance level to imazamox and mesosulfuron, evaluate other herbicide options for the control of these multiple resistant L. perenne ssp. multiflorum, and characterize the underlying ALS-inhibitor resistance mechanism(s). Based on LD50 values, the MR1-A, MR1-P, and MR2 subpopulations were 38-, 29-, 8-fold and 36-, 64-, and 3-fold less sensitive to imazamox and mesosulfuron, respectively, relative to the susceptible (Sus) population. Only MR1-P and MR2 plants were cross-resistant to rimsulfuron, whereas both MR1 subpopulations were cross-resistant to imazethapyr. Pinoxaden (ACCase inhibitor [phenylpyrazoline 'DEN']) only controlled MR2 and Sus plants at the labeled field rate. However, all plants were effectively controlled (>99%) with the labeled field rate of glufosinate. Based on I50 values, MR1-A, MR-P, and MR2 plants were 712-, 1,104-, and 3-fold and 10-, 18-, and 5-fold less responsive to mesosulfuron and imazamox, respectively, than the Sus plants. Sequence alignment of the ALS gene of resistant plants revealed a missense single-nucleotide polymorphism resulting in a Trp-574-Leu substitution in MR1-A and MR1-P plants, heterozygous in both, but not in the MR2 plants. An additional homozygous substitution, Asp-376-Glu, was identified in the MR1-A plants. Addition of malathion or piperonyl butoxide did not alter the efficacy of mesosulfuron on MR2 plants. In addition, the presence of 2,4-D had no effect on the response of mesosulfuron on the MR2 and Sus. These results suggest an altered target site is the mechanism of resistance to ALS inhibitors in MR1-A and MR1-P plants, whereas a non–target site based resistance apparatus is present in the MR2 plants.

Chloris spp. are warm-season grasses that outcompete crops for scarce resources throughout Australia. In Queensland, mild winters and increased adoption of conservation tillage practices have led to an increase of this warm-season grass family in winter crops. The objective of this study is to understand whether droplet size (nozzle type) effects herbicide efficacy of summer perennial grasses, as previous research found no effect of droplet size (nozzle type) on herbicide efficacy of winter annual grasses. A study to compare droplet-size (nozzle type) effects on control of windmillgrass and its domesticated relative, rhodesgrass, was conducted at the University of Queensland in Gatton, QLD, Australia. Results showed little difference in dry weight reductions for windmillgrass or rhodesgrass across droplet size (nozzle type). Paraquat applications with the TTI nozzle resulted in significantly lower dry weight reductions compared with other droplet-size sprays (nozzle types) for rhodesgrass. Glyphosate, imazamox plus imazapyr, and clodinafop resulted in commercially acceptable control for both species, regardless of the droplet size (nozzle type) selected, indicating droplet size (nozzle type) has relatively little impact on the efficacy of these herbicides. Proper nozzle selection can result in control of Chloris spp., a hard to control weed species, while reducing the occurrence of spray drift to nearby sensitive areas.

Herbicide resistance, and in particular multiple-herbicide resistance, poses an ever-increasing threat to food security. A biotype of junglerice [Echinochloa colona (L.) Link] with resistance to four herbicides, imazamox, fenoxaprop-P-ethyl, quinclorac, and propanil, each representing a different mechanism of action, was identified in Sunflower County, MS. Dose responses were performed on the resistant biotype and a biotype sensitive to all four herbicides to determine the level of resistance. Application of a cytochrome P450 inhibitor, malathion, with the herbicides imazamox and quinclorac resulted in increased susceptibility in the resistant biotype. Differential gene expression analysis of resistant and sensitive plants revealed that 170 transcripts were upregulated in resistant plants relative to sensitive plants and 160 transcripts were upregulated in sensitive plants. In addition, 507 transcripts were only expressed in resistant plants and 562 only in sensitive plants. A subset of these transcripts were investigated further using quantitative PCR (qPCR) to compare gene expression in resistant plants with expression in additional sensitive biotypes. The qPCR analysis identified two transcripts, a kinase and a glutathione S-transferase that were significantly upregulated in resistant plants compared with the sensitive plants. A third transcript, encoding an F-box protein, was downregulated in the resistant plants relative to the sensitive plants. As no cytochrome P450s were differentially expressed between the resistant and sensitive plants, a single-nucleotide polymorphism analysis was performed, revealing several nonsynonymous point mutations of interest. These candidate genes will require further study to elucidate the resistance mechanisms present in the resistant biotype.

Imazapyr and imazamox are frequently applied postemergence to control grass and broadleaf weeds in imidazolinone-resistant sunflower in Argentina. Herbicide carryover to rotational crops represents a disadvantage of these herbicides, particularly in regions with low rainfall during the months prior to rotational crop sowing. Between 2009 and 2012, field and greenhouse studies were conducted on four important sunflower-cropped areas of Argentina. The objective was to quantify the effects of imazapyr alone and imazamox plus imazapyr applied in sunflower crops on the subsequent establishment, growth, and yield of barley, oat, and wheat. In all field experiments, imazapyr alone and imazamox plus imazapyr were applied at recommended rates (80 gha–1 and 66 plus 30 gha–1, respectively), and also, in some experiments, at double the recommended rates. Soil bioassays were also conducted in the greenhouse to study the effect of these herbicides on barley, oat, and wheat seedlings. The mixture of imazamox plus imazapyr was safer for rotational crops than imazapyr applied alone, because of the reduced rate of imazapyr in the mixture treatments. Barley was more sensitive to imidazolinones, particularly imazapyr, than the other winter cereals. Imazapyr at double rate (160 gha–1) reduced barley yield by 45% when seeds were sown 165 d after herbicide application and with 240 mm rainfall after herbicide application.

A false cleavers population that survived treatment with triasulfuron/bromoxynil in 1996 was identified in central Alberta, Canada, in a field that had been treated with acetolactate synthase (ALS) inhibitors in 3 of the previous 6 yr. In greenhouse studies, this biotype was highly resistant to the ALS inhibitors triasulfuron, thifensulfuron/tribenuron, and sulfometuron and moderately resistant to imazethapyr; GR50, values were > 16, > 5, > 1.0, and 9.9, respectively. In addition, cross-resistance was identified to the auxin-type herbicide quinclorac (GR50 value > 6.7) but not to fluroxypyr (GR50 value 1) or MCPA/mecoprop/dicamba. Quinclorac had not been used previously in this field. Analysis of ALS extracted from the resistant biotype and a susceptible biotype from a nearby location indicated that resistance to ALS inhibitors was due to an altered target site with reduced sensitivity to a broad range of ALS inhibitors. The ALS I50 values for triasulfuron, metsulfuron, chlorsulfuron, thifensulfuron, and imazethapyr were 36, 34, 92, 96, and 14 times higher, respectively, for the resistant compared to the susceptible biotype. The mechanism of resistance to quinclorac is unknown. This is the first report of high-level herbicide resistance in this weed species.

Greenhouse studies were conducted to evaluate potential interactions among glyphosate mixtures with five acetolactate synthase (ALS)-inhibiting herbicides (chlorimuron, imazamox, imazaquin, MON 12,000, or pyrithiobac) for the control of purple nutsedge and sicklepod at two growth stages. Herbicides were tested alone at 0.5X and 1X rates (1X being suggested use rate for these herbicides) and in combination with glyphosate at 560 (0.5X) and 1,120 (1X) g ai/ha on 3-wk-old plants and at 1,120 g/ha on 6-wk-old plants. Glyphosate alone at 1,120 g/ha gave complete control of purple nutsedge and at least 78% control of sicklepod regardless of growth stage. In 3-wk-old purple nutsedge plants, three of the 20 herbicide combinations were antagonistic and 17 combinations were additive, whereas all five combinations were additive in 6-wk-old plants. In sicklepod, eight combinations were antagonistic and 12 combinations were additive in 3-wk-old plants, and all five combinations were antagonistic in 6-wk-old plants. In 3-wk-old plants, the glyphosate (0.5X) plus imazaquin (0.5X) combination resulted in highest antagonism in purple nutsedge control (79%), and the combination of glyphosate (0.5X) plus imazamox (0.5X) resulted in highest antagonism in sicklepod control (54%). These results indicate that mixing chlorimuron, imazamox, imazaquin, MON 12,000, or pyrithiobac with glyphosate does not increase glyphosate efficacy on purple nutsedge or sicklepod.

Field and greenhouse studies were conducted in 1995 and 1996 in Kansas to determine the efficacy of 21 herbicide treatments for control of tumble pigweed, Palmer amaranth, redroot pigweed, and two biotypes of common waterhemp in soybean. In field studies, nine of eleven preemergence treatments controlled all four species 90% or more. However, pendimethalin and trifluralin controlled Palmer amaranth, redroot pigweed, and tumble pigweed less than the other preplant incorporated and preemergence treatments. With the exception of flumiclorac and NAF-75, postemergence treatments controlled 75 to 90% of all four species. A biotype of common waterhemp collected in Iowa was not controlled by acetolactate synthase-inhibiting herbicides. Greenhouse results were similar to field experiments. Results suggest at least 90% control of these Amaranthus species is possible with proper herbicide selection.

Acetolactate synthase (ALS)-inhibiting herbicide carryover in soil can severely affect sugarbeets grown in the year(s) following application. Two newly developed imidazolinone-resistant (IMI-R) sugarbeet somatic cell selections (Sir-13 and 93R30B) were examined for magnitude of resistance and extent of cross-resistance to other classes of ALS inhibitors and compared to a previously developed sulfonylurea-resistant (SU-R) selection, Sur. In vitro shoot culture tests indicated Sir-13 resistance was specific to imidazolinone (IMI) herbicides at approximately a 100-fold resistance compared to the sensitive control sugarbeet. Sur was 10,000-fold resistant to the sulfonylurea (SU) herbicide, chlorsulfuron, and 40-fold resistant to the triazolopyrimidine sulfonanilide (TP) herbicide, flumetsulam, but not cross-resistant to the IMI herbicides. 93R30B was selected for IMI-R from a plant homozygous for the SU-R allele, Sur, and displayed similar in vitro SU-R and TP-R as Sur, but also displayed a very high resistance to various IMI herbicides (400- to 3,600-fold). Compared to the sensitive control, Sir-13 was 300- and > 250-fold more resistant to imazethapyr and imazamox residues in soil, respectively. Response by whole plants to postemergence herbicide applications was similar to that observed in shoot cultures. Sir-13 exhibited > 100-fold resistance to imazethapyr as well as imazamox, and 93R30B showed > 250-fold resistance to both herbicides. 93R30B showed great enough resistance to imazamox to merit consideration of imazamox for use as a herbicide in these sugarbeets. Sir-13 showed a two- to threefold higher level of resistance in the homozygous vs. heterozygous state, indicating that like most ALS-inhibitor resistance traits, it was semidominantly inherited.

Parasitic witchweeds inflict most of their damage while still underground and attached to crop roots. Most selective translocated herbicides are detoxified by crops such as corn and thus cannot reach the attached parasites. Corn with target site resistance to acetolactate synthase (ALS)-inhibiting herbicides was tested to ascertain whether these herbicides could control witchweeds, assuming that witchweeds do not obtain amino acids from the crop. Postemergence directed sprays of 27 g ae ha−1 imazapyr 54 d after planting (DAP) delayed Striga asiatica emergence on corn in South Carolina from 3 wk (control) to 7 wk and to 11 wk when mixed with 45 g ae ha−1 AC 263 222. Treatments with up to 71 g ae ha−1 imazamox, and up to 71 g ae ha−1 AC 263 222 only delayed Striga emergence by 1 wk, and 71 g ae ha−1 imazethapyr was ineffective. ALS-inhibiting herbicides were far more effective when applied in 1-ml drenches above the seed at planting. Chlorsulfuron (10 g ai ha−1) and sulfometuron (50 g ai ha−1) were somewhat phytotoxic to Pioneer 3245IR. Rimsulfuron (30 g ai ha−1), metsulfuron (10 g ai ha−1), halosulfuron (120 g ai ha−1), and imazethapyr (140 g ae ha−1) were marginally active in Kenya, with some mature Striga hermonthica seed-bearing capsules appearing at harvest (12 wk). Imazapyr at 15 g ae ha−1 gave 70 to 95% suppression of capsule formation, whereas no capsules appeared at 30 g ae ha−1. The use of imazapyr in Kenya increased the harvest index by 17% when corn plants in Striga-infested soils were kept insect and disease free by using insecticides and fungicides. Thus, complete control can be achieved at affordable cost by farmers in subsistence conditions.

A plant response study was conducted in the greenhouse to evaluate interactions between imazamox and acifluorfen, fomesafen, or lactofen. Antagonistic interactions between imazamox and acifluorfen or fomesafen affected control of I. hederacea and A. theophrasti 21 d after treatment. Combinations of imazamox plus lactofen also antagonized control of I. hederacea. I. hederacea absorbed less 14C-imazamox when applied with nonlabeled acifluorfen, but absorption by A. theophrasti was not affected by the combination. Addition of nonlabeled lactofen did not affect absorption of imazamox in A. theophrasti or I. hederacea. Addition of acifluorfen or lactofen reduced translocation of 14C-imazamox to foliage above and below the treated leaf and the root in both A. theophrasti and I. hederacea. Antagonism of A. theophrasti control was due to reduced translocation of imazamox. Antagonism of I. hederacea control was due to reduced translocation of imazamox when applied with lactofen or reduced absorption and translocation when applied with acifluorfen.