Amaranth Populations Research Articles

Palmer Amaranth in the Pacific Northwest

AbstractPalmer amaranth is one of the most troublesome pigweeds in crop production systems in the United States. It only recently started to appear in the Pacific Northwest (PNW). A coordinated extension and outreach effort among land grant universities (University of Idaho, Oregon State University, and Washington State University), Amalgamated Sugar, other commodity commissions, and industry was launched to track Palmer amaranth in the PNW. In 2023, tissue samples were collected from pigweeds suspected to be Palmer amaranth with tests providing confirmation. Palmer amaranth was detected in several crops as well as right‐of‐way and private property. Most of the Palmer amaranth populations were confirmed to be resistant to glyphosate. Additional surveys and resistance screening efforts are underway to map the distribution of Palmer amaranth and assess the level of herbicide resistance across the region. Earn 0.5 CEUs in Integrated Pest Management by reading this article and taking the quiz at https://web.sciencesocieties.org/Learning‐Center/Courses.

Influence of gender and glyphosate resistance on Palmer amaranth growth and interference with cotton

AbstractManagement of herbicide‐resistant weeds can be improved by understanding the biology of resistant biotypes. While the majority of research has focused on female plants and seed production of Palmer amaranth (Amaranthus palmeri S. Watson) that are resistant to glyphosate, growth of male plants that are resistant to this herbicide has not been studied in detail. Additionally, interference of male versus female Palmer amaranth plants on cotton (Gossypium hirsutum) yield has not been reported. Plant height and biomass of male and female plants from a mixed population of glyphosate‐resistant (GR) and glyphosate‐susceptible (GS) plants was studied in North Carolina when grown season‐long with cotton. Palmer amaranth height was less for GR male plants compared with GS males and both GR and GS females. Biomass of Palmer amaranth female plants was twice that of male plants irrespective of glyphosate resistance. Cotton yield was affected similarly by Palmer amaranth regardless of either gender or glyphosate resistance status. The implications of shorter GR male plants on pollen dispersal and ramifications on management of glyphosate resistance are not known. Results from these trials did not address implications of the height of male plants on fitness of GR resistance. Nonetheless, the finding that GR male plants were shorter in the field than GS male plants warrants a new look at this topic. Similar reductions for cotton yield in presence of both GR and GS biotypes and genders suggest that current yield loss assessments and management decisions do not need to consider these variables in Palmer amaranth populations.

Multiple resistance to EPSPS and ALS inhibitors in Palmer amaranth (Amaranthus palmeri) identified in Turkey

AbstractAmaranthus palmeri was first reported in Turkey in 2016, and an immediate heavy infestation of the weed was found in fruit orchards and summer crops such as maize, cotton, and sunflower. There have been farmers' complaints about the ineffective control of Palmer amaranth through the use of glyphosate and some sulfonylureas herbicides. Hence, this study aimed to determine the possible herbicide resistance evolution in Palmer amaranth against glyphosate and acetolactate synthase (ALS) herbicides. Seeds of 21 Palmer amaranth populations were collected from five provinces of Turkey where control problems with glyphosate and ALS inhibitors were reported in maize fields. Seeds of certain biotypes categorized as resistant or susceptible were grown to obtain the F2 generation. A single‐dose experiment determined the possible resistance to ALS inhibitors and glyphosate among the 21 populations. Of this, 18 populations were included in the subsequent dose–response experiments due to evident survival. Based on ED50 values from the dose–response experiment, SNU‐04 and ADN‐21 biotypes had the highest resistance index for glyphosate which was more than 7. The biotypes ADN‐21, OSM‐15, and DIR‐09 recorded the highest ED50 value with a resistance index of 9.21–10.35 after nicosulfuron application. Whereas, the biotypes SNU‐04, OSM‐15, and ADN‐21 were with the highest ED50 value and resistance index of 6.41–7.44, after the application of foramsulfuron + iodosulfuron methyl‐sodium. The increase in genomic 5‐enolpyruvylshikimate‐3‐phosphate synthase (EPSPS) copy number has been observed in suspected cases that have been accepted as the molecular basis for the development of resistance against glyphosate. The sequence alignment results for the ALS gene contained Ala122Val and Pro197Arg mutations related to target‐site resistance against ALS herbicides.

Metabolism of the 4-Hydroxyphenylpyruvate Dioxygenase Inhibitor, Mesotrione, in Multiple-Herbicide-Resistant Palmer amaranth (Amaranthus palmeri).

Metabolic resistance to the maize-selective, HPPD-inhibiting herbicide, mesotrione, occurs via Phase I ring hydroxylation in resistant waterhemp and Palmer amaranth; however, mesotrione detoxification pathways post-Phase I are unknown. This research aims to (1) evaluate Palmer amaranth populations for mesotrione resistance via survivorship, foliar injury, and aboveground biomass, (2) determine mesotrione metabolism rates in Palmer amaranth populations during a time course, and (3) identify mesotrione metabolites including and beyond Phase I oxidation. The Palmer amaranth populations, SYNR1 and SYNR2, exhibited higher survival rates (100%), aboveground biomass (c.a. 50%), and lower injury (25-30%) following mesotrione treatment than other populations studied. These two populations also metabolized mesotrione 2-fold faster than sensitive populations, PPI1 and PPI2, and rapidly formed 4-OH-mesotrione. Additionally, SYNR1 and SYNR2 formed 5-OH-mesotrione, which is not produced in high abundance in waterhemp or naturally tolerant maize. Metabolite features derived from 4/5-OH-mesotrione and potential Phase II mesotrione-conjugates were detected and characterized by liquid chromatography-mass spectrometry (LCMS).

Comparison of residual activity of pre‐emergence herbicides for control and seed production of multiple herbicide‐resistant Palmer amaranth in food‐grade white corn

AbstractNebraska is the number‐one producer of food‐grade white corn (Zea mays L.) in the United States. Food‐grade white corn has not been genetically engineered; therefore, non‐selective herbicides such as glyphosate or glufosinate cannot be used. Multiple herbicide‐resistant (MHR) Palmer amaranth (Amaranthus palmeri S. Watson) populations have been reported in multiple counties in Nebraska, and their management is a challenge, particularly for white corn producers. The objectives of this study were to evaluate the residual activity of pre‐emergence (PRE) herbicides for acetolactate synthase inhibitor (halosulfuron‐methyl)/atrazine/glyphosate‐resistant Palmer amaranth control, density, biomass, seed production, and grain yield in food‐grade white corn. Field experiments were conducted during summer 2020 and 2021 in a grower's field infested with MHR Palmer amaranth near Carleton, NE. All the PRE herbicides resulted in similar control (>90%) 30 days after PRE application (DAPRE) apart from atrazine (64%). At 45 DAPRE, acetochlor/mesotrione, atrazine/bicyclopyrone/mesotrione/S‐metolachlor, and acetochlor/clopyralid/mesotrione controlled 90%–95% Palmer amaranth. Acetochlor/clopyralid/mesotrione and atrazine/bicyclopyrone/mesotrione/S‐metolachlor provided 96%–99% MHR Palmer amaranth control and reduced Palmer amaranth density and biomass to 2–4 plants m−2 and 5–12 g m−2 60 DAPRE. The highest corn yields of 12,139 kg ha−1 and 12,093 kg ha−1 in 2020 and 2021, respectively, were obtained with acetochlor/clopyralid/mesotrione. Palmer amaranth seed production was least with acetochlor/clopyralid/mesotrione (32,894 seeds m−2). Tested residual PRE herbicides did not show corn injury and were safe to use in food‐grade white corn. It is concluded that acetochlor/clopyralid/mesotrione and atrazine/bicyclopyone/mesotrione/S‐metolachlor are the best options for early season control of MHR Palmer amaranth in food‐grade white corn.

Metabolic Resistance to Protoporphyrinogen Oxidase-Inhibitor Herbicides in a Palmer amaranth Population from Kansas.

Palmer amaranth has evolved target and nontarget site resistance to protoporphyrinogen oxidase-inhibitor herbicides in the United States. Recently, a population (KCTR) from a long-term conservation tillage study in Kansas was found to be resistant to herbicides from six sites of action, including to PPO-inhibitors, even with this herbicide group being minimally used in this field. This research investigated the level of resistance to postemergence PPO-inhibitors, target- and nontarget-site resistance mechanism(s), and efficacy of pre-emergence chemistries. The greenhouse experiments confirmed 6.1- to 78.9-fold resistance to lactofen in KCTR, with the level of resistance increasing when KCTR was purified for the resistance trait. PPO2 sequences alignment revealed the absence of known mutations conferring resistance to PPO-inhibitors in KCTR Palmer amaranth, and differential expression of the PPO2 gene did not occur. KCTR metabolized fomesafen faster than the susceptible population, indicating that herbicide detoxification is the mechanism conferring resistance in this population. Further, treatment with the cytochrome P450-inhibitor malathion followed by lactofen restored the sensitivity of KCTR to this herbicide. Despite being resistant to POST applied PPO-inhibitors, KCTR Palmer amaranth was completely controlled by the labeled rate of the PRE applied PPO-inhibitors fomesafen, flumioxazin, saflufenacil, sulfentrazone, and oxadiazon. The overall results suggest that P450-mediated metabolism confers resistance to PPO-inhibitors in KCTR, rather than alterations in the PPO2, which were more commonly found in other Palmer amaranth populations. Future work will focus on identifying the fomesafen metabolites and on unravelling the genetic basis of metabolic resistance to PPO-inhibitor herbicides in KCTR Palmer amaranth.

Confirming resistance to PPO-inhibiting herbicides applied preemergence and postemergence in a Georgia Palmer amaranth population

Abstract Herbicides that inhibit protoporphyrinogen oxidase (PPO) are used in more than 40 agronomic and specialty crops across Georgia to manage weeds through residual and postemergence (POST) control. In 2017, a population of Palmer amaranth exhibiting reduced sensitivity to POST applications of PPO-inhibiting herbicides was identified by the University of Georgia. Seed were collected from the site along with a known sensitive population; distance between the samples was 200 m, increasing the likelihood of similar environmental and genetic characteristics. To quantify sensitivity for both preemergence (PRE) and POST uses, 21 greenhouse dose-response assessments were conducted from 2017 to 2022. After conducting initial rate-response studies, 13 doses per herbicide were chosen for the POST experiment; field use rates of fomesafen (420 g ai ha−1), lactofen (219 g ai ha−1), acifluorfen (420 g ai ha−1), and trifludimoxazin (25 g ai ha−1) ranging from 0× to 4× the field use rate for the susceptible population, and 0× to 40× for the suspect population were applied. Herbicide treatments included adjuvants and were applied to plants 8 to 10 cm in height. Relative resistance factors (RRFs) were calculated for control ratings, mortality, and biomass, and ranged from 105 to 318, 36 to 1,477, 215 to 316, and 9 to 49 for fomesafen, lactofen, acifluorfen, and trifludimoxazin, respectively. In the PRE experiment, herbicide applications included five to nine doses of fomesafen (1× = 210 g ai ha−1), flumioxazin (1× = 57 g ai ha−1), oxyfluorfen (1× = 561 g ai ha−1), and trifludimoxazin (1× = 38 g ai ha−1); doses ranged from 0× to 6× for the suspect population and 0× to 2× for the susceptible population. Visual control, mortality, and biomass RRFs ranged from 3 to 5 for fomesafen, 21 to 31 for flumioxazin, 6 to 22 for oxyfluorfen, and 8 to 38 for trifludimoxazin. Results confirm that a Georgia Palmer amaranth population is resistant to PPO-inhibiting herbicides applied both PRE and POST.

Spray interval, application order, and plant height influences control of dicamba-resistant Palmer amaranth

Abstract Palmer amaranth, which is resistant to glyphosate and protoporphyrinogen oxidase inhibitors, remains a threat to cotton and soybean production in Tennessee. This is partly due to the recent evolution of dicamba-resistant Palmer amaranth in western Tennessee, which further complicates weed management. Experiments were conducted in 2021 and 2022 to determine the best timing between sequential applications and the order in which 2,4-D or dicamba should be used with glufosinate to control resistant Palmer amaranth. Palmer amaranth control increased when the interval between postemergence herbicide applications decreased from 21 to 7 d. At the 7-d interval in a dicamba-based system, the order of herbicides did not affect Palmer amaranth control. However, in a 2,4-D-based system, the greatest control was achieved when 2,4-D was applied first, followed by either 2,4-D or glufosinate. While weed height at the time of application had a significant effect on Palmer amaranth control with auxin herbicides, control was still unacceptable in the field at the labeled rates of dicamba or 2,4-D when applied to weeds that were <10 cm tall (48% and 53%, respectively). Neither dicamba nor 2,4-D provided acceptable control of the Palmer amaranth populations evaluated in this study. Sequential applications separated by 7 d provided better weed control than those separated by 21 d. Given that the better 7-d sequential treatments provided less than 90% control and resulted in more than 64,000 surviving Palmer amaranth plants per hectare suggests that relying solely on these herbicides for Palmer amaranth control is not a sustainable weed management strategy.

Baseline survey reveals glyphosate and dicamba resistance in broadleaf weeds before sugar beet trait introduction

Abstract A prelaunch survey of broadleaf weeds was conducted to predict the weed management efficacy of a novel genetically engineered sugar beet with resistance traits for glyphosate, dicamba, and glufosinate. We targeted problematic broadleaf weed species prevalent in sugar beet fields, including kochia, common lambsquarters, Palmer amaranth, and redroot pigweed in Colorado, Nebraska, and Wyoming. The results revealed that a significant percentage of kochia populations in Colorado, Nebraska, and Wyoming exhibited resistance to glyphosate (94%, 98%, and 75%, respectively) and dicamba (30%, 42%, and 17%, respectively). Palmer amaranth populations had resistance frequencies for glyphosate and dicamba of 80% and 20% in Colorado and 20% and 3% in Nebraska, respectively. No resistance to the tested herbicides was identified in common lambsquarters or redroot pigweed. Glufosinate resistance was not identified for any species. Kochia and Palmer amaranth populations from Colorado and Nebraska exhibited glyphosate resistance primarily through 5-enolpyruvylshikimate-3-phosphate synthase (EPSPS) gene amplification. However, one glyphosate-resistant kochia population from Wyoming lacked EPSPS gene amplification, indicating the presence of an alternative resistance mechanism. We identified the previously characterized IAA16 G73N substitution in a dicamba-resistant kochia population from Nebraska. However, dicamba-resistant kochia populations from Colorado did not possess this substitution, suggesting an alternative, yet-to-be-determined resistance mechanism. The widespread prevalence of glyphosate and dicamba resistance, coupled with the emergence of novel resistance mechanisms, poses a significant challenge to the long-term efficacy of this novel genetically engineered sugar beet technology. These findings underscore the urgent need for integrated weed management strategies that diversify effective herbicide sites-of-action and incorporate alternative weed management practices within cropping systems.

Non–target site mechanisms of cross-resistance evolution to florpyrauxifen-benzyl in 2,4-D–resistant Palmer amaranth (Amaranthus palmeri)

AbstractThe evolution of herbicide resistance in weeds can reduce the herbicide’s efficacy, depleting crop yield and quality. Our group previously confirmed 2,4-D resistance in three Palmer amaranth (Amaranthus palmeri S. Watson) populations (R1 to R3). In the current study, the first filial (F1) seeds of 2,4-D–resistant populations were subjected to screening tests for resistance to other auxin-mimicking herbicides, florpyrauxifen-benzyl (FPB; 30 g ai ha−1) and dicamba (560 g ae ha−1). Dicamba killed all resistant populations. FPB provided 100% control of only the R3 population. Sensitivities to FPB were reduced by 2 and 35 percentage points in R1 and R2 populations, respectively. Pretreatment with malathion increased FPB sensitivity by 15 percentage points in the R2 population. FPB resistance characterization and mechanism were evaluated using a purified line of the R2 population (F2). The FPB sensitivity was 29-fold lower in the F2 line than in the susceptible (S) standard. Absorption, translocation, and total metabolism of FPB were similar for S and R2 populations. However, less florpyrauxifen-acid (FPA) was detected in the R2 population (17.0% to 25.4%) than in the S population (22.8% to 33.2%), due to its rapid metabolism and/or reduced production with resistance evolution. Because the results of the non–target site resistance mechanism evaluation observed in this study were insufficient to account for the 29-fold reduced sensitivity of the R2 population to FPB, further genetic studies are needed to investigate the presence of target-site resistance in that population.

Response of dicamba-resistant Palmer amaranth and cotton to malathion applied in conjunction with dicamba

Abstract Cotton and soybean growers were offered new technologies in 2016, expanding in-crop herbicide options to include dicamba or 2,4-D. Within 3 yr of commercialization, dicamba use in these crops increased 10-fold, and growers began to report Palmer amaranth escapes in dicamba-tolerant production systems in western Tennessee. In 2020, Palmer amaranth seed was collected from eight Tennessee locations where growers witnessed poor control following dicamba. Greenhouse experiments were conducted to evaluate the response of these Palmer amaranth populations to dicamba. In 2021, field experiments were conducted on two tentative dicamba-susceptible populations in Georgia, on three confirmed dicamba-resistant populations in Tennessee, and on a tentative dicamba-susceptible population in Texas to evaluate cotton response following dicamba and to examine if malathion insecticide (a cytochrome P450 inhibitor) would improve weed control and not reduce cotton yield when applied in conjunction with dicamba. Palmer amaranth populations collected in 2020 survived dicamba in the greenhouse at 1, 2, and 4 times the labeled rate. Five Palmer amaranth populations exhibited 15% to 26% survival to the labeled dicamba rate (560 g ha−1) in the greenhouse. These findings were reinforced in the field when research on three of those populations in 2021 showed 55% control with the labeled dicamba rate and 69% control with 2 times the labeled rate. This demonstrates that the dicamba resistance allele or alleles were passed between generations. This result was not consistent in the Macon County, GA, or Worth County, GA, locations, where malathion improved dicamba control of 15- to 38-cm-tall Palmer amaranth. Cotton injury was observed when malathion was applied in combination with dicamba. These results further document the evolution of dicamba-resistant Palmer amaranth in Tennessee. Moreover, the nonreversal of resistance phenotype by malathion may suggest that the resistance mechanism is something other than metabolism.

Global Metabolome of Palmer Amaranth (Amaranthus palmeri) Populations Highlights the Specificity and Inducibility of Phytochemical Responses to Abiotic Stress.

Commonalities in adaptive responses to abiotic stressors could contribute to the development of cross-resistance in weeds. The degree to which herbicide-induced changes in weeds parallel those induced by other abiotic stress remains unknown. We investigated the specificity of metabolic perturbations induced by glyphosate and drought across three glyphosate-resistant (GR) and two glyphosate-susceptible (GS) biotypes of Palmer amaranth (Amaranthus palmeri) using global metabolomics approaches. Compared to GS-biotypes, in the absence of stress, the GR-biotypes had a higher abundance of primary metabolites, including sugars, nonaromatic amino acids, and organic acids. However, despite having a higher 5-enolpyruvylshikimate-3-phosphate synthase (EPSPS) gene copy number that could upregulate the phenylpropanoid metabolism, the nonstressed GR-biotypes were less abundant in specialized (secondary) metabolites. Under glyphosate stress, 80% of metabolites, including shikimate, that accumulated in GS-biotypes also increased in the GR-biotypes. However, glyphosate triggered the preferential accumulation of glycosides of dihydroxylated and methoxylated flavanols with higher antioxidant potential, and ferulic acid derivatives, specifically in GR-biotypes. The disruption of the shikimate pathway and the accumulation of phenylpropanoids upon glyphosate exposure suggest that the stress response of GR-biotypes could be partly induced. This differential response was less evident in other phytochemical classes and under drought, highlighting that the phytochemical responses are stress-specific rather than biotype-specific.

Effects of elevated CO2 on the response of glyphosate resistant and susceptible Palmer amaranth (Amaranthus palmeri S. Wats.) to varying rates of glyphosate

ABSTRACT Repeated application of herbicides has led to herbicide-resistant weed populations. Elevated CO2 often increases weed growth, exacerbating problems including impacts on crop yield and weed control. How rising CO2 affects herbicide-resistant weeds remains largely unknown. Palmer amaranth (Amaranthus palmeri) populations resistant to or susceptible to glyphosate were exposed to ambient or elevated (ambient +200 μmol mol−1) concentrations of CO2 in open-top chambers. Two weeks after CO2 exposure, each population was sprayed with glyphosate at 0, 0.5×, 1.0×, or 1.5× the label rate. Afterwards, CO2 exposure continued for an additional two weeks when visual herbicide injury and leaf gas exchange were assessed. Plants were harvested for determination of treatment effects on growth. Elevated CO2 had little effect on most variables except for decreasing stomatal conductance (~25.5%) and increasing water use efficiency (~49.2%). Glyphosate resistant plants showed decreased height (9.8%) and damage (~56.4%) and increased root dry weight (12.1%), photosynthesis (~41.2%), stomatal conductance (~63.3%), and water use efficiency (~32.0%). In general, increasing rates of glyphosate decreased growth and gas exchange variables, which was frequently only seen in the susceptible ecotype. Data suggest that rising atmospheric CO2 is unlikely to affect Palmer amaranth, including control of glyphosate-resistant populations.

Impact of integrated weed management practices on cotton economics and Palmer amaranth (Amaranthus palmeri) populations

AbstractThe threat of herbicide-resistant weed species, such as Palmer amaranth, has driven the development of robust weed management programs that rely on more than chemicals for weed control. Previous research has shown that zero-tolerance weed thresholds, cover crops, deep tillage, and diverse herbicide programs are effective strategies for controlling Palmer amaranth. Unfortunately, research investigating the integration of all four of these weed management strategies in a system is lacking. To better leverage these integrated weed management strategies in cotton production systems, a long-term study was initiated in fall 2018 near Marianna, AR, with zero tolerance, deep tillage, a cereal rye cover crop, and either a dicamba or non-dicamba in-crop herbicide program as factors. Results found that total Palmer amaranth emergence was reduced 76% as the result of deep tillage in 2019 and, in the absence of a zero-tolerance strategy, 73% in 2020. In the absence of a zero-tolerance strategy, the combination of a non–cover crop strategy and dicamba herbicide program decreased total Palmer amaranth emergence by 73%, while the combination of a cover crop strategy and dicamba herbicide program decreased total Palmer amaranth emergence by 78% compared to the combination of a cover crop and non-dicamba herbicide program. Under a zero-tolerance strategy in 2019, tillage reduced cotton yield by 12% and partial returns by US$370 ha−1. In 2020, tillage reduced cotton yield by 14% and partial returns of US$371 ha−1 under a non-zero-tolerance strategy, while a 12% yield reduction and a US$260 ha−1 decrease in partial returns were observed under a zero-tolerance strategy. In 2019, the non-dicamba program resulted in greater partial returns than the dicamba in-crop program because of greater yield and lower program costs. However, in 2020, partial returns were greater for the dicamba in-crop herbicide program owing to greater yields achieved by this program.

Rapid metabolism and increased expression of CYP81E8 gene confer high level of resistance to tembotrione in a multiple-resistant Palmer amaranth (Amaranthus palmeri S. Watson)

Herbicides, such as tembotrione, that inhibit 4-hydroxyphenylpyruvate dioxygenase (HPPD) enzyme are used to control broad spectrum of weeds, primarily in corn, as this crop can metabolize these herbicides via cytochrome P450 activity. In 2018, a Palmer amaranth (Amaranthus palmeri) population, KCTR was found to be resistant to multiple herbicides including, tembotrione in Kansas (KS), USA. However, the mechanism of tembotrione resistance in KCTR is not known. The objective of this study was to characterize the level of tembotrione resistance and investigate the mechanism of resistance to this herbicide in KCTR using a known susceptible Palmer amaranth population (KSS). Tembotrione dose response experiments revealed that KCTR Palmer amaranth is 23 times more resistant to this herbicide, than KSS. No difference in absorption or translocation of [14C] tembotrione between KSS and KCTR was found. However, the time required to metabolize 50% of tembotrione was shorter in KCTR than in KSS. More than 95% of tembotrione was metabolized at 6 hours after treatment (HAT) in the KCTR, compared to only 50% in KSS plants. Application of cytochrome P450-inhibitors (e.g., malathion or piperonyl butoxide), along with tembotrione reversed the resistance in KCTR. Furthermore, the KCTR plants showed 35-fold increase in constitutive expression of CYP81E8 gene compared to KSS. Nonetheless, the HPPD gene expression was not altered in KCTR Palmer amaranth. Our results suggest that enhanced metabolism of tembotrione possibly due to increased expression of CYP81E8 gene contribute to tembotrione resistance in KCTR. Metabolic resistance to herbicides is a challenge for weed management as such resistance predisposes weeds to evolve resistance to unknown herbicides even without selection.

Resistance to 2,4-D in Palmer amaranth (Amaranthus palmeri) from Kansas is mediated by enhanced metabolism

AbstractA Palmer amaranth (Amaranthus palmeri S. Watson) population (KCTR: KS Conservation Tillage Resistant) collected from a conservation tillage field was confirmed with resistance to herbicides targeting at least six sites of action, including 2,4-D. The objectives of this research were using KCTR A. palmeri to investigate (1) the level of 2,4-D resistance, (2) 2,4-D absorption and translocation profiles, (3) the rate of 2,4-D metabolism compared with 2,4-D–tolerant wheat (Triticum aestivum L.), and (4) the possible role of cytochrome P450s (P450s) in mediating resistance. Dose–response experiments were conducted to assess the level of 2,4-D resistance in KCTR compared with susceptible plants, KSS (KS 2,4-D susceptible) and MSS (MS 2,4-D susceptible). KSS, MSS, and KCTR plants were treated with [14C]2,4-D to determine absorption, translocation, and metabolic patterns. Additionally, whole-plant dose–response assays were conducted by treating KCTR and KSS plants with P450 inhibitors (malathion, piperonyl butoxide [PBO]) before 2,4-D application. Dose–response experiments indicated a 6- to 11-fold 2,4-D resistance in KCTR compared with susceptible plants. No difference was found in percent [14C]2,4-D absorption among the populations. However, 10% less and 3 times slower translocation of [14C]2,4-D was found in KCTR compared with susceptible plants. Importantly, [14C]2,4-D was metabolized faster in KCTR than susceptible plants. At 24, 48, and 72 h after treatment (HAT), KCTR metabolized ∼20% to 30% more [14C]2,4-D than susceptible plants. KCTR plants and wheat generated metabolites with similar polarity. Nonetheless, at 24 HAT, ∼70% of [14C]2,4-D was metabolized in wheat, compared with only 30% in KCTR A. palmeri. Application of malathion before 2,4-D increased the sensitivity to 2,4-D in KCTR, suggesting involvement of P450s in mediating 2,4-D metabolism. However, no such impact of PBO was documented. Overall, this study confirms that enhanced metabolism is the primary mechanism of 2,4-D resistance in KCTR.

Transpiration Responses of Herbicide-Resistant and -Susceptible Palmer Amaranth (Amaranthus palmeri (S.) Wats.) to Progressively Drying Soil

Drought events are predicted to increase in the future. Evaluating the response of herbicide-resistant and -susceptible weed ecotypes to progressive drought can provide insights into whether resistance traits affect the fitness of resistant weed populations. Two experiments were conducted in the greenhouse between January and May 2021 to evaluate drought tolerance differences between Palmer amaranth accessions resistant to S-metolachlor or glyphosate and their susceptible counterparts. The accessions used were S-metolachlor-resistant (17TUN-A), a susceptible standard (09CRW-A), and glyphosate-resistant (22–165 EPSPS copies) and glyphosate-susceptible (3–10 EPSPS copies) plants from accession 16CRW-D. Daily transpiration of each plant was measured. The daily transpiration rate was converted to normalized transpiration ratio (NTR) using a double-normalization procedure. The daily soil water content was expressed as a fraction of transpirable soil water (FTSW). The threshold FTSW (FTSWcr), after which NTR decreases linearly, was estimated using a two-segment linear regression analysis. The data showed differences between S-metolachlor-resistant and -susceptible accessions (p ≤ 0.05). The FTSW remaining in the soil at the breakpoint for the S-metolachlor-susceptible accession (09CRW-A) was 0.17 ± 0.007. The FTSW remaining in the soil at the breakpoint for the S-metolachlor-resistant accession (17TUN-A) was 0.23 ± 0.004. The FTSW remaining in the soil at the breakpoint for the glyphosate-resistant and glyphosate-susceptible plants (16CRW-D) was 0.25 ± 0.007 and 0.25 ± 0.008, respectively. Although the mechanism endowing resistance to S-metolachlor might have contributed to increased drought tolerance, follow-up experiments are needed in order to verify this finding. Increased EPSPS copy numbers did not improve the drought tolerance of Palmer amaranth. As droughts are predicted to increase in frequency and severity, these results suggest that S-metolachlor-resistant and glyphosate-resistant Palmer amaranth populations will not be at a competitive disadvantage compared to susceptible genotypes. Alternative and diverse management strategies will be required for effective Palmer amaranth control, regardless of herbicide resistance status.

A nonnative Palmer amaranth (Amaranthus palmeri) population in the Republic of South Africa is resistant to herbicides with different sites of action

AbstractPalmer amaranth (Amaranthus palmeriS. Watson) is not native to Africa. Based on the presence and persistence ofA. palmeripopulations, its invasive status in southern Africa is classified as “naturalized.” Globally,A. palmeriis one of the most troublesome weed species in several crops, including soybean [Glycine max(L.) Merr.], maize (Zea maysL.), and cotton (Gossypium hirsutumL.). Certain populations ofA. palmeriin various countries were reported to be resistant to herbicides with different sites of action (SOAs). Two biotypes ofA. palmeriin the United States reportedly each have resistance to herbicides representing five different SOAs, and between them a total of eight different SOAs are involved. Resistance mechanisms in these biotypes involve target-site and/or non–target site resistance. Here we characterize a specificA. palmeripopulation that was found in the Douglas district in South Africa and showed resistance to various herbicide SOAs. Initially, thisA. palmeripopulation was discovered in a glyphosate-tolerant cotton field, where it survived glyphosate treatment. Subsequently, greenhouse experiments were conducted to characterize thisA. palmeripopulation for potential resistance to herbicides of additional SOAs, and molecular analyses were conducted to reveal the mechanisms of herbicide resistance. Results indicated resistance to chlorimuron-ethyl and glyphosate in this population, while <90% control (decreased sensitivity) was observed at the label rate for mesotrione, atrazine, saflufenacil, andS-metolachlor. However, glufosinate, tembotrione, acifluorfen, dicamba, 2,4-D, metribuzin, acetochlor, isoxaflutole, diflufenican, and pyroxasulfone were effective at controlling this population. This profiling of herbicide sensitivity has allowed development of programs to control and potentially minimize the spread of this weed. In addition, molecular analysis ofEPSPSrevealed the role of higher copy number as a mechanism for glyphosate resistance in this population and a Ser-653-Asn target-site mutation likely conferring resistance to the acetolactate synthase–inhibitor chlorimuron-ethyl. No known target-site mutations were identified for the protoporphyrinogen oxidase–inhibitor group.

Assessing the Weed-Suppressing Potential of Cotton Chromosome Substitution Lines Using the Stair-Step Assay.

Palmer amaranth is a problematic common weed species, especially in cotton. With the wide use of chemical herbicide and herbicide-tolerant transgenic cotton lines, Palmer amaranth populations have developed tolerance to commonly used herbicides. It is imperative to develop alternative weed control methods to slow the evolution of herbicide-resistant weed populations and provide new strategies for weed management. Eleven chromosome substitution (CS) cotton lines (CS-B26Lo, CS-T17, CS-B16-15, CS-B17-11, CS-B12, CS-T05sh, CS-T26Lo, CS-T11sh, CS-M11sh, CS-B22sh, and CS-B22Lo) were screened for weed-suppressing abilities in this study. The cotton lines were tested using the established stair-step assay. Height (cm) and chlorophyll concentration (cci) were measured for each plant in the system. The most significant variation in Palmer amaranth height reduction among the CS lines was observed 21 days after establishment. CS-B22sh (76.82%) and CS-T26Lo (68.32%) were most effective in reducing Palmer amaranth height. The cluster analysis revealed that CS-B22sh, and CS-T26Lo were clustered in one group, suggesting similar genetic potential with reference to Palmer amaranth growth and development. CS-B22sh showed novel genetic potential to control the growth and development of Palmer amaranth, a problematic weed in cotton fields. Future experimentation should implement more parameters and chemical testing to explore allelopathic interactions among CS lines and Palmer amaranth.

Emergence pattern and periodicity of Palmer amaranth (Amaranthus palmeri) populations from southcentral Great Plains

AbstractEvolution of multiple herbicide–resistant Palmer amaranth warrants the development of integrated strategies for its control in the southcentral Great Plains (SGP). To develop effective control strategies, a better understanding of the emergence biology of Palmer amaranth populations from the SGP region is needed. A common garden study was conducted in a no-till (NT) fallow field at the Kansas State University Agricultural Research Center near Hays, KS, during the 2018 and 2019 growing seasons, to determine the emergence pattern and periodicity of Palmer amaranth populations collected from the SGP region. Nine Palmer amaranth populations collected from five states were included: Colorado (CO1, CO2), Oklahoma (OK), Kansas (KS1, KS2), Texas (TX), and Nebraska (NE1, NE2, NE3). During the 2018 growing season, the CO1 and KS1 populations displayed more rapid emergence rates, with greater parameter b values (−5.4, and −5.3, respectively), whereas the TX and NE3 populations had the highest emergence rates (b = −12.2) in the 2019 growing season. The cumulative growing degree days (cGDD) required to achieve 10%, 50%, and 90% cumulative emergence ranged from 125 to 144, 190 to 254, and 285 to 445 in 2018; and 54 to 74, 88 to 160, and 105 to 420 in the 2019 growing season across all tested populations, respectively. The OK population exhibited the longest emergence duration (301 and 359 cGDD) in both growing seasons. All tested Palmer amaranth populations had a peak emergence period between May 11 and June 8 in 2018, and April 30 and June 1 in the 2019 growing season. Altogether, these results indicate the existence of differential emergence pattern and peak emergence periods of geographically distant Palmer amaranth populations from the SGP region. This information will help in developing prediction models for decision-making tools to manage Palmer amaranth in the region.