Rapid vegetative growth and adverse application conditions are common factors leading to the failure of postemergence herbicides on Palmer amaranth. A sequential herbicide application, or respray, is often necessary to control weeds that have survived the initial herbicide application to protect crop yield and minimize weed seed production. The optimum timing after the initial application and the most effective herbicide for control of Palmer amaranth has not been characterized. The objectives of these experiments were to determine the optimum herbicide for treating Palmer amaranth regrowth, the optimum timing for each of those herbicides, and how the initial failed herbicide might affect efficacy of a second herbicide application. Bare ground field experiments were performed in 2017 and 2018 in which glufosinate or fomesafen herbicide failure was induced on Palmer amaranth plants that were 30 cm in height. Respray treatments of glufosinate, fomesafen, lactofen, 2,4-D, and dicamba were applied once at timings of 4 to 5 d, 7 d, or 11 d after the initial spray application. Nearly all herbicide treatment and timing combinations increased control by at least 13 percentage points compared to no respray herbicide treatment. Regardless of initial herbicide, glufosinate applied as a respray treatment was the most consistent and efficacious with up to 97% control. The specific herbicide used in the second application impacted final weed control more so than timing of the respray application. For instance, control by glufosinate respray treatments was 10 to 18 percentage points greater than control from lactofen respray treatments, whereas control decreased by 3 percentage points when respray applications of any herbicide were made 11 d after initial application of glufosinate compared to 4 to 5 and 7 d after initial application of glufosinate. In the event of failure to control Palmer amaranth with glufosinate or fomesafen, glufosinate should be applied in order to maximize control.

Conservation tillage adoption continues to be threatened by glyphosate and acetolactate synthase–resistant Palmer amaranth and other troublesome weeds. Field experiments were conducted from autumn 2010 through crop harvest in 2013 at two locations in Alabama to evaluate the effect of integrated management practices on weed control and seed cotton yield in glyphosate-resistant cotton. The effects of a cereal rye cover crop using high- or low-biomass residue, followed by wide or narrow within-row strip tillage and three PRE herbicide regimens were evaluated. The three PRE regimens were (1) pendimethalin at 0.84 kg ae ha−1 plus fomesafen at 0.28 kg ai ha−1 applied broadcast, (2) pendimethalin plus fomesafen applied banded on the row, or (3) no PRE. Each PRE treatment was followed by (fb) glyphosate (1.12 kg ae ha−1) applied POST fb layby applications of diuron (1.12 kg ai ha−1) plus monosodium methanearsonate (2.24 kg ai ha−1). Low-residue plots ranged in biomass from 85 to 464 kg ha−1, and high-biomass residue plots ranged from 3,119 to 6,929 kg ha−1. In most comparisons, surface disturbance width, residue amount, and soil-applied herbicide placement did not influence within-row weed control; however, broadcast PRE resulted in increased carpetweed, large crabgrass, Palmer amaranth, tall morning-glory, and yellow nutsedge weed control in row middles compared with plots receiving banded PRE. In addition, high-residue plots had increased carpetweed, common purslane, large crabgrass, Palmer amaranth, sicklepod, and tall morning-glory weed control between rows. Use of banded PRE herbicides resulted in equivalent yield and revenue in four of six comparisons compared with those with broadcast PRE herbicide application; however, this would likely result in many between-row weed escapes. Thus, conservation tillage cotton would benefit from broadcast soil-applied herbicide applications regardless of residue amount and tillage width when infested with Palmer amaranth and other troublesome weed species.

Glyphosate-resistant (GR) Palmer amaranth is a troublesome weed that can emerge throughout the soybean growing season in Nebraska and several other regions of the United States. Late-emerging Palmer amaranth plants can produce seeds, thus replenishing the soil seedbank. The objectives of this study were to evaluate single or sequential applications of labeled POST herbicides such as acifluorfen, dicamba, a fomesafen and fluthiacet-methyl premix, glyphosate, and lactofen on GR Palmer amaranth control, density, biomass, seed production, and seed viability, as well as grain yield of dicamba- and glyphosate-resistant (DGR) soybean. Field experiments were conducted in a grower’s field infested with GR Palmer amaranth near Carleton, NE, in 2018 and 2019, with no PRE herbicide applied. Acifluorfen, dicamba, a premix of fomesafen and fluthiacet-methyl, glyphosate, or lactofen were applied POST in single or sequential applications between the V4 and R6 soybean growth stages, with timings based on product labels. Dicamba applied at V4 or in sequential applications at V4 followed by R1 or R3 controlled GR Palmer amaranth 91% to 100% at soybean harvest, reduced Palmer amaranth density to as low as 2 or fewer plants m−2, reduced seed production to 557 to 2,911 seeds per female plant, and resulted in the highest soybean yield during both years of the study. Sequential applications of acifluorfen, fomesafen and fluthiacet premix, or lactofen were not as effective as dicamba for GR Palmer amaranth control; however, they reduced seed production similar to dicamba. On the basis of the results of this study, we conclude that dicamba was effective for controlling GR Palmer amaranth and reduced density, biomass, and seed production without DGR soybean injury. Herbicides evaluated in this study had no effect on Palmer amaranth seed viability.

Palmer amaranth is the latest pigweed species documented in Connecticut; it was identified there in 2019. In a single-dose experiment, the Connecticut Palmer amaranth biotype survived the field-use rates of glyphosate (840 g ae ha−1) and imazaquin (137 g ai ha−1) herbicides applied separately. Additional experiments were conducted to (1) determine the level of resistance to glyphosate and acetolactate synthase (ALS) inhibitors in the Connecticut-resistant (CT-Res) biotype using whole-plant dose-response bioassays, and (2) evaluate the response of the CT-Res biotype to POST herbicides commonly used in Connecticut cropping systems. Based on the effective dose required for 90% control (ED90), the CT-Res biotype was 10-fold resistant to glyphosate when compared with the Kansas-susceptible (KS-Sus) biotype. Furthermore, the CT-Res biotype was highly resistant to ALS-inhibitor herbicides; only 18% control was achieved with 2,196 g ai ha−1 imazaquin. The CT-Res biotype was also cross-resistant to other ALS-inhibitor herbicides, including chlorimuron-ethyl (13.1 g ai ha−1), halosulfuron-methyl (70 g ai ha−1), and sulfometuron-methyl (392 g ai ha−1). The CT-Res Palmer amaranth was controlled 75% to 100% at 21 d after treatment (DAT) with POST applications of 2,4-D (386 g ae ha−1), carfentrazone-ethyl (34 g ai ha−1), clopyralid (280 g ae ha−1), dicamba (280 g ae ha−1), glufosinate (595 g ai ha−1), lactofen (220 g ai ha−1), oxyfluorfen (1,121g ai ha−1), and mesotrione (105 g ai ha−1) herbicides. Atrazine (2,240 g ai ha−1) controlled the CT-Res biotype only 52%, suggesting the biotype is resistant to this herbicide as well. Here we report the first case of Palmer amaranth from Connecticut with multiple resistance to glyphosate and ALS inhibitors. Growers should proactively use all available weed control tactics, including the use of effective PRE and alternative POST herbicides (tested in this study), for effective control of the CT-Res biotype.

A prepackaged mixture of desmedipham + phenmedipham was previously labeled for control of Amaranthus spp. in sugarbeet. Currently, there are no effective POST herbicide options to control glyphosate-resistant Palmer amaranth in sugarbeet. Sugarbeet growers are interested in using desmedipham + phenmedipham to control escaped Palmer amaranth. In 2019, a greenhouse experiment was initiated near Scottsbluff, NE, to determine the selectivity of desmedipham and phenmedipham between Palmer amaranth and sugarbeet. Three populations of Palmer amaranth and four sugarbeet hybrids were evaluated. Herbicide treatments consisted of desmedipham and phenmedipham applied singly or as mixtures at an equivalent rate. Herbicides were applied when Palmer amaranth and sugarbeet were at the cotyledon stage, or two true-leaf sugarbeet stage and when Palmer amaranth was 7 cm tall. The selectivity indices for desmedipham, phenmedipham, and desmedipham + phenmedipham were 1.61, 2.47, and 3.05, respectively, at the cotyledon stage. At the two true-leaf application stage, the highest rates of desmedipham and phenmedipham were associated with low mortality rates in sugarbeet, resulting in a failed response of death. The highest rates of desmedipham + phenmedipham caused a death response of sugarbeet; the selectivity index was 2.15. Desmedipham treatments resulted in lower LD50 estimates for Palmer amaranth compared to phenmedipham, indicating that desmedipham can provide greater levels of control for Palmer amaranth. However, desmedipham also caused greater injury in sugarbeet, producing lower LD50 estimates compared to phenmedipham. Desmedipham + phenmedipham provided 90% or greater control of cotyledon-size Palmer amaranth at a labeled rate but also caused high levels of sugarbeet injury. Neither desmedipham, phenmedipham, nor desmedipham + phenmedipham was able to control 7-cm tall Palmer amaranth at previously labeled rates. Results indicate that desmedipham + phenmedipham can only control Palmer amaranth if applied at the cotyledon stage and a high level of sugarbeet injury is acceptable.

The evolution of multiple herbicide-resistant weeds, including Palmer amaranth, has necessitated the implementation of an integrated weed management (IWM) program. Understanding weed emergence patterns is critical for developing effective IWM strategies. The objective of this study was to evaluate the effect of tillage timings and residual herbicides on cumulative emergence and emergence pattern of Palmer amaranth. Field experiments were conducted in 2015 and 2016 in a field naturally infested with photosystem (PS) II and 4-hydroxyphenylpyruvate dioxygenase (HPPD) inhibitor-resistant Palmer amaranth near Shickley, Nebraska, in a bare ground study, with no crop planted in the plots, although residues from the preceding corn crop were present on the soil surface. Treatments consisted of shallow tillage timings (early, mid, and late), three premix corn or soybean residual herbicides, and a nontreated control. The Weibull function was fitted to cumulative Palmer amaranth emergence with day of year (DOY) and thermal time (TT) as independent variables. Year by treatment interaction was significant for time to 10%, 25%, 50%, 75%, and 90% Palmer amaranth emergence and cumulative emergence. The majority of Palmer amaranth seedlings emerged early, following early tillage with 90% cumulative emergence occurring on DOY 172 compared with DOY 210 to 212 for mid- and late-tillage, and DOY 194 for the nontreated control in 2015. In 2016, 90% of cumulative emergence following early-, mid-, and late-tillage (DOYs 201 to 211) were similar, and that of the nontreated control (DOY 188) was similar to that of early tillage. Nontreated control and PRE herbicide treatments had similar DOY values for 90% emergence in both years. The number of emerged Palmer amaranth seedlings over the season was higher with shallow tillage than no tillage or with the use of PRE herbicides.

Palmer amaranth is an extremely troublesome weed for soybean growers because of its aggressive growth, adaptability, prolific seed production, and widespread resistance to many herbicides. Studies were initiated to determine the effects of herbicide application at first female inflorescence on Palmer amaranth control, biomass, seed production, cumulative germination, and seed viability. Enlist (2,4-D–resistant) soybean and Xtend (dicamba-resistant) soybean were planted and various combinations of either 2,4-D or dicamba with and without glufosinate and/or glyphosate were applied at first visible female Palmer amaranth inflorescence. Mixtures of 2,4-D + glufosinate and 2,4-D + glufosinate + glyphosate provided the greatest control at 4 wk after treatment in Enlist soybean. Similarly, in Xtend soybean, combinations of dicamba + glufosinate and dicamba + glufosinate + glyphosate provided the greatest control. The greatest reductions in biomass were from combinations of auxin herbicides (2,4-D or dicamba) plus glufosinate with and without glyphosate. Seed production was reduced most by treatments containing at least one effective site of action: an auxin herbicide (2,4-D or dicamba) or glufosinate. In contrast to previous research, cumulative germination and seed viability were not affected by herbicide treatments. This research indicates the efficacy of auxin herbicides or glufosinate alone and in combination to reduce the seed production of Palmer amaranth when applied at first female inflorescence. More research is needed to evaluate the full potential for applications of these herbicides at flower initiation to mitigate the evolution of herbicide resistance.

Weed control of paraquat can be erratic and may be attributable to differing species sensitivity and/or environmental factors for which minor guidance is available on commercial labels. Therefore, the objectives of this research were to quantify selectivity of paraquat across select weed species and the influence of environmental factors. Experiments were performed under controlled conditions in the greenhouse and growth chamber. Compared with purple deadnettle (dose necessary to reduce shoot biomass by 50% = 39 g ai ha−1), waterhemp, Palmer amaranth, giant ragweed, and horseweed were 4.9, 3.3, 1.9, and 1.3 times more sensitive to paraquat, respectively. The injury progression rate over 3 d after treatment (DAT) was a more accurate predictor of final efficacy at 14 DAT than the lag phase until symptoms first appeared. For example, at the 17.5 g ha−1 dose, the injury rate of waterhemp and Palmer amaranth was, on average, 3.6 times greater than that of horseweed and purple deadnettle. The influence of various environmental factors on paraquat efficacy was weed specific. Applications made at sunrise improved control of purple deadnettle over applications at solar noon or sunset. Lower light intensities (200 or 600 μmol m−2 s−1) surrounding the time of application improved control of waterhemp and horseweed more than 1,000 μmol m−2 s−1. Day/night temperatures of 27/16 C improved horseweed and purple deadnettle control compared with day/night temperatures of 18/13 C. Though control was positively associated with injury rates in the application time of day and temperature experiments, a negative relationship was observed for waterhemp in the light-intensity experiment. Thus, although there are conditions that enhance paraquat efficacy, the specific target species must also be considered. These results advocate paraquat dose recommendations, currently based on weed height, be expanded to address sensitivity differences among weeds. Moreover, these findings contrast with paraquat labels stating temperatures of 13 C or lower do not reduce paraquat efficacy.

Residual herbicides applied PRE provide early season weed control, potentially avoid the need for multiple POST herbicides, and can provide additional control of herbicide-resistant weeds. Thus, field studies were conducted in 2017 and 2018 at Concord, NE, to evaluate the influence of PRE herbicides on critical time for postemergence weed removal (CTWR) in corn. The studies were arranged in a split-plot design that consisted of three herbicide regimes as main plot treatments and seven weed removal timings as subplot treatments in four replications. The herbicide regimes included no PRE herbicide, atrazine, and a premix of saflufenacil/dimethenamid-P mixed with pyroxasulfone. The weed removal timings were at V3, V6, V9, V12, and V15 corn growth stages and then plots were kept weed-free until harvest. A weed-free and nontreated control were included for comparison. The relationship between corn growth or yield, and weed removal timings in growing degree days (GDD) was described by a four-parameter log-logistic model. This model was used to estimate the critical time for weed removal based on 5% crop yield loss threshold. A delay in weed removal until the V2 to V3 corn growth stage (91 to 126 GDD) reduced corn biomass by 5% without PRE herbicide application. The CTWR started at V3 without PRE herbicide in both years. Atrazine delayed the CTWR up to V5 in both years, whereas saflufenacil/dimethenamid-P plus pyroxasulfone further delayed the CTWR up to the V10 and V8 corn growth stages in 2017 and 2018, respectively. Herbicide applied PRE particularly with multiple sites of action can delay the CTWR in corn up to a maximum growth stage of V10, and delay or reduce the need for POST weed management.

Pollen-mediated gene flow (PMGF) refers to the transfer of genetic information (alleles) from one plant to another compatible plant. With the evolution of herbicide-resistant (HR) weeds, PMGF plays an important role in the transfer of resistance alleles from HR to susceptible weeds; however, little attention is given to this topic. The objective of this work was to review reproductive biology, PMGF studies, and interspecific hybridization, as well as potential for herbicide resistance alleles to transfer in the economically important broadleaf weeds including common lambsquarters, giant ragweed, horseweed, kochia, Palmer amaranth, and waterhemp. The PMGF studies involving these species reveal that transfer of herbicide resistance alleles routinely occurs under field conditions and is influenced by several factors, such as reproductive biology, environment, and production practices. Interspecific hybridization studies within Amaranthus and Ambrosia spp. show that herbicide resistance allele transfer is possible between species of the same genus but at relatively low levels. The widespread occurrence of HR weed populations and high genetic diversity is at least partly due to PMGF, particularly in dioecious species such as Palmer amaranth and waterhemp compared with monoecious species such as common lambsquarters and horseweed. Prolific pollen production in giant ragweed contributes to PMGF. Kochia, a wind-pollinated species can efficiently disseminate herbicide resistance alleles via both PMGF and tumbleweed seed dispersal, resulting in widespread occurrence of multiple HR kochia populations. The findings from this review verify that intra- and interspecific gene flow can occur and, even at a low rate, could contribute to the rapid spread of herbicide resistance alleles. More research is needed to determine the role of PMGF in transferring multiple herbicide resistance alleles at the landscape level.

Trifludimoxazin, a new protoporphyrinogen oxidase–inhibiting herbicide, is being evaluated for possible use as a soil-residual active herbicide treatment in cotton for control of small-seeded annual broadleaf weeds. Laboratory and greenhouse studies were conducted to compare vertical mobility and cotton tolerance of trifludimoxazin to flumioxazin and saflufenacil, which are two currently registered protoporphyrinogen oxidase–inhibiting herbicides for use in cotton, in three West Texas soils. Vertical soil mobility of trifludimoxazin was similar to flumioxazin in Acuff loam and Olton loam soils, but was more mobile than flumioxazin in the Amarillo loamy sand soil. The depth of trifludimoxazin movement after a 2.5-cm irrigation event ranged from 2.5 to 5.0 cm in all soils, which would not allow for crop selectivity based on herbicide placement, because ideal cotton seeding depth is from 0.6 to 2.54 cm deep. Greenhouse studies indicated that PRE treatments were more injurious than the 14 d preplant treatment when summarized across soils for the three herbicides (43% and 14% injury, respectively). No differences in visual cotton response or dry weight was observed after trifludimoxazin preplant as compared with the nontreated control within each of the three West Texas soils and was similar to the flumioxazin preplant across soils. On the basis of these results, a use pattern for trifludimoxazin in cotton may be established with the use of a more than 14-d preplant restriction before cotton planting.

Field experiments were conducted in 2018 and 2019 at Kansas State University Ashland Bottoms (KSU-AB) research farm near Manhattan, KS, and Kansas State University Agricultural Research Center (KSU-ARC) near Hays, KS, to determine the effectiveness of various PRE-applied herbicide premixes and tank mixtures alone or followed by (fb) an early POST (EPOST) treatment of glyphosate + dicamba for controlling glyphosate-resistant (GR) Palmer amaranth in glyphosate/dicamba-resistant (GDR) soybean. In experiment 1, PRE-applied sulfentrazone + S-metolachlor, saflufenacil + imazethapyr + pyroxasulfone, chlorimuron + flumioxazin + pyroxasulfone, and metribuzin + flumioxazin + imazethapyr provided 85% to 94% end-of-season control of GR Palmer amaranth across both sites. In comparison, Palmer amaranth control ranged from 63% to 87% at final evaluation with PRE-applied pyroxasulfone + sulfentrazone, pyroxasulfone + sulfentrazone plus metribuzin, pyroxasulfone + sulfentrazone plus carfentrazone + sulfentrazone, and sulfentrazone + metribuzin at the KSU-ARC site in experiment 2. All PRE fb EPOST (i.e., two-pass) programs provided near-complete (98% to 100%) control of GR Palmer amaranth at both sites. PRE-alone programs reduced Palmer amaranth shoot biomass by 35% to 76% in experiment 1 at both sites, whereas all two-pass programs prevented Palmer amaranth biomass production. No differences in soybean yields were observed among tested programs in experiment 1 at KSU-ARC site; however, PRE-alone sulfentrazone + S-metolachlor, saflufenacil + imazethapyr + pyroxasulfone, and chlorimuron + flumioxazin + pyroxasulfone had lower grain yield (average, 4,342 kg ha−1) compared with the top yielding (4,832 kg ha−1) treatment at the KSU-AB site. PRE-applied sulfentrazone + metribuzin had a lower soybean yield (1,776 kg ha−1) compared with all other programs in experiment 2 at the KSU-ARC site. These results suggest growers should proactively adopt effective PRE-applied premixes fb EPOST programs evaluated in this study to reduce selection pressure from multiple POST dicamba applications for GR Palmer amaranth control in GDR soybean.

Overreliance on herbicides for weed control has led to the evolution of herbicide-resistant Palmer amaranth populations. Farm managers should consider the long-term consequences of their short-term management decisions, especially when considering the soil weed seedbank. The objectives of this research were to (1) determine how soybean population and POST herbicide application timing affects in-season Palmer amaranth control and soybean yield, and (2) how those variables influence Palmer amaranth densities and cotton yields the following season. Soybeans were planted (19-cm row spacing) at a low-, medium-, and high-density population (268,000, 546,000, and 778,000 plants ha–1, respectively). Fomesafen and clethodim (280 and 210 g ai ha–1, respectively) were applied at the VE, V1, or V2 to V3 soybean growth stage. Nontreated plots were also included to assess the effect of soybean population alone. The following season, cotton was planted into these plots so as to understand the effects of soybean planting population on Palmer amaranth densities in the subsequent crop. When an herbicide application occurred at the V1 or V2 to V3 soybean stage, weed control in the high-density soybean population increased 17% to 23% compared to the low-density population. Economic return was not influenced by soybean population and was increased 72% to 94% with herbicide application compared to no treatment. In the subsequent cotton crop, Palmer amaranth densities were 24% to 39% lower 3 wk after planting when following soybean sprayed with herbicides compared to soybean without herbicides. Additionally, Palmer amaranth densities in cotton were 19% lower when soybean was treated at the VE stage compared to later stages. Thus, increasing soybean population can improve Palmer amaranth control without adversely affecting economic returns and can reduce future weed densities. Reducing the weed seedbank and selection pressure from herbicides are critical in mitigating resistance evolution.

Glyphosate-resistant (GR) Palmer amaranth is a problematic, annual broadleaf weed in soybean production fields in Nebraska and many other states in the United States. Soybean resistant to 2,4-D, glyphosate, and glufosinate (Enlist E3TM) has been developed and was first grown commercially in 2019. The objectives of this research were to evaluate the effect of herbicide programs applied PRE, PRE followed by (fb) late-POST (LPOST), and early-POST (EPOST) fb LPOST on GR Palmer amaranth control, density, and biomass reduction, soybean injury, and yield. Field experiments were conducted near Carleton, NE, in 2018, and 2019 in a grower’s field infested with GR Palmer amaranth in 2,4-D–, glyphosate-, and glufosinate-resistant soybean. Sulfentrazone + cloransulam-methyl, imazethapyr + saflufenacil + pyroxasulfone, and chlorimuron ethyl + flumioxazin + metribuzin applied PRE provided 84% to 97% control of GR Palmer amaranth compared with the nontreated control 14 d after PRE. Averaged across herbicide programs, PRE fb 2,4-D and/or glufosinate, and sequential application of 2,4-D or glufosinate applied EPOST fb LPOST resulted in 92% and 88% control of GR Palmer amaranth, respectively, compared with 62% control with PRE-only programs 14 d after LPOST. Reductions in Palmer amaranth biomass followed the same trend; however, Palmer amaranth density was reduced 98% in EPOST fb LPOST programs compared with 91% reduction in PRE fb LPOST and 76% reduction in PRE-only programs. PRE fb LPOST and EPOST fb LPOST programs resulted in an average soybean yield of 4,478 and 4,706 kg ha−1, respectively, compared with 3,043 kg ha−1 in PRE-only programs. Herbicide programs evaluated in this study resulted in no soybean injury. The results of this research illustrate that herbicide programs are available for the management of GR Palmer amaranth in 2,4-D–, glyphosate-, and glufosinate-resistant soybean.

During the 2017 to 2019 growing seasons, samples of waterhemp and Palmer amaranth that had reportedly survived field-rate applications of protoporphyrinogen oxidase (PPO)–inhibiting herbicides were collected from the American Midwest and tested for target-site mutations known at the time to confer resistance. Target-site resistance was identified in nearly all (135 of 145) tested common waterhemp populations but in only 8 of 13 Palmer amaranth populations. Follow-up research on one population of Palmer amaranth (W-8), which tested negative for all such mutations, confirmed it was resistant to lactofen, with a magnitude of resistance comparable to that conferred by the ΔG210 PPO2 mutation. Gene sequences from both isoforms of PPO (PPO1 and PPO2) were compared between W-8 and known PPO inhibitor–sensitive sequence. A glycine-to-alanine substitution at the 399th amino acid position (G399A) of PPO2, recently identified to reduce target-site herbicide sensitivity, was observed in a subset of resistant W-8 plants. Because no missense mutation completely delimited resistant and sensitive sequences, we initially suspected the presence of a secondary, non-target-site resistance mechanism in this population. To isolate G399A, a segregating F2 population was produced and screened with a delimiting rate of lactofen. χ2 goodness-of-fit analysis of dead/alive ratings indicated single-locus inheritance of resistance in the F2 population, and molecular markers for the W-8 parental PPO2 coding region co-segregated tightly, but not perfectly, with resistance. More research is needed to fully characterize Palmer amaranth PPO inhibitor–resistance mechanisms, which appear to be more diverse than those found in common waterhemp.

Field studies were conducted in 2018 and 2019 in Arkansas, Indiana, Illinois, Missouri, and Tennessee to determine if cover-crop residue interfered with herbicides that provide residual control of Palmer amaranth and waterhemp in no-till soybean. The experiments were established in the fall with planting of cover crops (cereal rye + hairy vetch). Herbicide treatments consisted of a nontreated or no residual, acetochlor, dimethenamid-P, flumioxazin, pyroxasulfone + flumioxazin, pendimethalin, metribuzin, pyroxasulfone, and S-metolachlor. Palmer amaranth took 18 d and waterhemp took 24 d in the cover crop–alone (nontreated) treatment to reach a height of 10 cm. Compared with this treatment, all herbicides except metribuzin increased the number of days until 10-cm Palmer amaranth was present. Flumioxazin applied alone or in a mixture with pyroxasulfone were the best at delaying Palmer amaranth growing to a height of 10 cm (35 d and 33 d, respectively). The herbicides that resulted in the lowest Palmer amaranth density (1.5 to 4 times less) integrated with a cover crop were pyroxasulfone + flumioxazin, flumioxazin, pyroxasulfone, and acetochlor. Those four herbicide treatments also delayed Palmer amaranth emergence for the longest period (27 to 34 d). Waterhemp density was 7 to 14 times less with acetochlor than all the other herbicides present. Yield differences were observed for locations with waterhemp. This research supports previous research indicating that utilizing soil-residual herbicides along with cover crops improves control of Palmer amaranth and/or waterhemp.

Since the release of dicamba-tolerant cotton in 2016, preplant and POST applications of dicamba to control glyphosate-resistant Palmer amaranth have increased. With the increase in area treated with dicamba, the risk of off-target movement to nontarget crops has increased. A field study was conducted at the Texas Tech University New Deal Research Farm equipped with subsurface drip irrigation in 2017 and 2018 to evaluate non-dicamba tolerant cotton response to dicamba when applied at four crop growth stages [first square (FS) + 2 wk, first bloom (FB), FB + 2 wk, and FB + 5 wk]. Dicamba at 0.56 (1×), 0.056 (1/10×), 0.0112 (1/50×), 0.0056 (1/100×), and 0.00112 (1/500×) kg ae ha−1 was applied to ‘FM 1830GLT’ cotton. When applications were made at FS + 2 wk, a shift in boll nodal position was apparent following dicamba at the 1/50× rate in 2017 and at 1/10× in 2018 compared to the nontreated control (NTC). A shift in boll distribution from the 1/50× rate of dicamba was apparent at FB in 2017, but not in 2018. Dicamba applied at the 1× rate at FB + 2 wk resulted in reduced boll numbers. No change in boll number or boll position was apparent following any dicamba rate when applied at FB + 5 wk in both years. Dicamba applied at 1/500×, 1/100×, and 1/50× rates at all timings did not affect yield relative to the NTC. When dicamba was applied at the 1/10× rate, the greatest yield loss was observed at FS + 2 wk followed by FB and FB + 2 wk. Micronaire increased following dicamba applied at 1/10× at FS + 2 wk, FB, and FB + 2 wk in 2017. In 2018, micronaire decreased following dicamba applied at 1/10× at FB + 5 wk.

Failure to control Palmer amaranth with glyphosate and protoporphyrinogen IX oxidase (PPO)-inhibitor herbicides was reported across southwestern Nebraska in 2017. The objectives of this study were to 1) confirm and 2) validate glyphosate and PPO-inhibitor (fomesafen and lactofen) resistance in 51 Palmer amaranth accessions from southwestern Nebraska using genotypic and whole-plant phenotypic assay correlations and cluster analysis, and 3) determine which agronomic practices might be influencing glyphosate resistance in Palmer amaranth accessions in that location. Based on genotypic assay, 88% of 51 accessions contained at least one individual with amplification (>2 copies) of the 5-enolypyruvyl-shikimate-3-phosphate synthase (EPSPS) gene, which confers glyphosate resistance; and/or a mutation in the PPX2 gene, either ΔG210 or R128G, which endows PPO-inhibitor resistance in Palmer amaranth. Cluster analysis and high correlation (0.83) between genotypic and phenotypic assays demonstrated that EPSPS gene amplification is the main glyphosate resistance mechanism in Palmer amaranth accessions from southwestern Nebraska. In contrast, there was poor association between genotypic and phenotypic responses for PPO-inhibitor resistance, which was attributed to segregation for PPO-inhibitor resistance within these accessions and/or the methodology that was adopted herein. Genotypic assays can expedite the process of confirming known glyphosate and PPO-inhibitor resistance mechanisms in Palmer amaranth from southwestern Nebraska and other locations. Phenotypic assays are also a robust method for confirming glyphosate resistance but not necessarily PPO-inhibitor resistance in Palmer amaranth. Moreover, random forest analysis of glyphosate resistance in Palmer amaranth indicated that EPSPS gene amplification, county, and current and previous crops are the main factors influencing glyphosate resistance within that geographic area. Most glyphosate-susceptible Palmer amaranth accessions were found in a few counties in areas with high crop diversity. Results presented here confirm the spread of glyphosate resistance and PPO-inhibitor resistance in Palmer amaranth accessions from southwestern Nebraska and demonstrate that less diverse cropping systems are an important driver of herbicide resistance evolution in Palmer amaranth.

The evolution of resistance to multiple herbicides in Palmer amaranth is a major challenge for its management. In this study, a Palmer amaranth population from Hutchinson, Kansas (HMR), was characterized for resistance to inhibitors of photosystem II (PSII) (e.g., atrazine), acetolactate synthase (ALS) (e.g., chlorsulfuron), and EPSP synthase (EPSPS) (e.g., glyphosate), and this resistance was investigated. About 100 HMR plants were treated with field-recommended doses (1×) of atrazine, chlorsulfuron, and glyphosate, separately along with Hutchinson multiple-herbicide (atrazine, chlorsulfuron, and glyphosate)–susceptible (HMS) Palmer amaranth as control. The mechanism of resistance to these herbicides was investigated by sequencing or amplifying the psbA, ALS, and EPSPS genes, the molecular targets of atrazine, chlorsulfuron, and glyphosate, respectively. Fifty-two percent of plants survived a 1× (2,240 g ai ha−1) atrazine application with no known psbA gene mutation, indicating the predominance of a non–target site resistance mechanism to this herbicide. Forty-two percent of plants survived a 1× (18 g ai ha−1) dose of chlorsulfuron with proline197serine, proline197threonine, proline197alanine, and proline197asparagine, or tryptophan574leucine mutations in the ALS gene. About 40% of the plants survived a 1× (840 g ae ha−1) dose of glyphosate with no known mutations in the EPSPS gene. Quantitative PCR results revealed increased EPSPS copy number (50 to 140) as the mechanism of glyphosate resistance in the survivors. The most important finding of this study was the evolution of resistance to at least two sites of action (SOAs) (~50% of plants) and to all three herbicides due to target site as well as non–target site mechanisms. The high incidence of individual plants with resistance to multiple SOAs poses a challenge for effective management of this weed.

Field studies were conducted to determine sweetpotato tolerance to and weed control from management systems that included linuron. Treatments included flumioxazin preplant (107 g ai ha−1) followed by (fb) S-metolachlor (800 g ai ha−1), oryzalin (840 g ai ha−1), or linuron (280, 420, 560, 700, and 840 g ai ha−1) alone or mixed with S-metolachlor or oryzalin applied 7 d after transplanting. Weeds did not emerge before the treatment applications. Two of the four field studies were maintained weed-free throughout the season to evaluate sweetpotato tolerance without weed interference. The herbicide program with the greatest sweetpotato yield was flumioxazin fb S-metolachlor. Mixing linuron with S-metolachlor did not improve Palmer amaranth management and decreased marketable yield by up to 28% compared with flumioxazin fb S-metolachlor. Thus, linuron should not be applied POST in sweetpotato if Palmer amaranth has not emerged at the time of application.