The critical period for weed control (CPWC) adds value to integrated weed management by identifying the period during which weeds need to be controlled to avoid yield losses exceeding a defined threshold. However, the traditional application of the CPWC does not identify the timing of control needed for weeds that emerge late in the critical period. In this study, CPWC models were developed from field data in high-yielding cotton crops during three summer seasons from 2005 to 2008, using the mimic weed, common sunflower, at densities of two to 20 plants per square meter. Common sunflower plants were introduced at up to 450 growing degree days (GDD) after crop planting and removed at successive 200 GDD intervals after introduction. The CPWC models were described using extended Gompertz and logistic functions that included weed density, time of weed introduction, and time of weed removal (logistic function only) in the relationships. The resulting models defined the CPWC for late-emerging weeds, identifying a period after weed emergence before weed control was required to prevent yield loss exceeding the yield-loss threshold. When weeds emerged in sufficient numbers toward the end of the critical period, the model predicted that crop yield loss resulting from competition by these weeds would not exceed the yield-loss threshold until well after the end of the CPWC. These findings support the traditional practice of ensuring weeds are controlled before crop canopy closure, with later weed control inputs used as required.

Few options are available for controlling bermudagrass invasion of seashore paspalum. Bermudagrass and seashore paspalum tolerance to topramezone, triclopyr, or the combination of these two herbicides were evaluated in both greenhouse and field conditions. Field treatments included two sequential applications of topramezone (15.6 g ai ha−1) alone and five rates of topramezone + triclopyr (15.6 + 43.2, 15.6 + 86.3, 15.6 + 172.6, 15.6 + 345.2, or 15.6 g ai ha−1 + 690.4 g ae ha−1). Secondary greenhouse treatments included a single application of topramezone (20.8 g ha−1) or triclopyr (258.9 g ha−1) alone, or in combination at 20.8 + 258.9 or 20.8 + 517.8 g ha−1, respectively. Greenhouse and field results showed that topramezone applications in combination with triclopyr present opposite responses between bermudagrass and seashore paspalum. Topramezone increased bermudagrass injury and decreased seashore paspalum bleaching injury compared to topramezone alone. In field evaluations, topramezone + triclopyr at 15.6 + 690.4 g ha−1 used in sequential applications resulted in >90% injury to bermudagrass, however, injury decreased over time. Furthermore, sequential applications of topramezone + triclopyr at 15.6 + 690.4 g ha−1 resulted in >50% injury to seashore paspalum. Application programs including topramezone plus triclopyr should increase bermudagrass suppression and reduce seashore paspalum injury compared to topramezone alone. However, additional studies are needed because such practices will likely require manipulation of topramezone rate, application timing, application interval, and number of applications in order to maximize bermudagrass control and minimize seashore paspalum injury.

Ludwigia prostrata is a problematic weed in rice fields in China, where acetolactate synthase (ALS)-inhibiting herbicides (e.g., bensulfuron-methyl) are widely used for the management of broadleaf weeds. Recently, an L. prostrata biotype (JS-R) that failed to be controlled with ALS-inhibiting herbicides was found in Jiangsu Province, China. This study aims to determine the level and molecular mechanism of resistance to bensulfuron-methyl in this JS-R biotype and to evaluate its spectrum of cross-resistance to other ALS-inhibiting herbicides. The dose–response assays indicated that the JS-R L. prostrata biotype had evolved 21.2-fold resistance to bensulfuron-methyl compared with the susceptible biotype (JS-S). ALS gene sequencing revealed that a nucleotide mutation (CCA to TCA) at codon 197, resulting in a Pro-197-Ser mutation, was detected in the resistant plants. Moreover, while the JS-R biotype contained the Pro-197-Ser resistance mutation and showed cross-resistance to pyrazosulfuron-ethyl (12.0-fold), it was sensitive to penoxsulam, bispyribac-sodium, and imazethapyr, which may serve as alternative herbicides to control the resistant L. prostrata biotype. This is the first confirmation of an L. prostrata biotype resistant to bensulfuron-methyl due to a Pro-197-Ser resistance mutation in the ALS gene.

Agricultural weeds remain an important production constraint, with labor shortages and a lack of new herbicide options in recent decades making the problem even more acute. Robotic weeding machines are a possible solution to these increasingly intractable weed problems. Franklin Robotics’ Tertill™ is an autonomous weeding robot designed for home gardeners that relies on a minimalistic design to be cost-effective. The objectives of this study were to investigate the ability of the Tertill to control broadleaf and grass weeds, and based on early observations, experiments were conducted with and without its string-trimmer–like weeding implement. Tertill demonstrated high weed-control efficacy, supporting its utility as a tool for home gardeners. Weeds were best controlled by the combined effect of soil disturbance caused by the action of the robot’s wheels and the actuation of the string trimmer. Despite the regrowth potential of an annual grass due to its meristem location, Tertill maintained low densities of millet in an experimental arena. The simple and effective design of the Tertill may offer insights to inform future development of farm-scale weeding robots. Weed density, emergence periodicity, robot working rate, and robotic weeding mechanisms are important design criteria regardless of the technology used for plant detection.

Amid widespread occurrence of herbicide-resistant weeds in the United States, the use of PRE herbicides and cover crops have resurged once again as important strategies for weed management in cropping systems. The objective of this experiment was to evaluate the length of soil residual weed control from PRE soybean herbicides and the detrimental impact of these herbicides on cover crop species using field treated soil in greenhouse bioassays. Greenhouse bioassays were conducted using soil from field experiments conducted in 2018 and 2019 in Arlington and Lancaster, WI. PRE herbicides consisted of imazethapyr, chlorimuron-ethyl, and cloransulam-methyl (acetolactate synthase [ALS] inhibitors); metribuzin (photosystem II [PS II] inhibitor); sulfentrazone, flumioxazin, and saflufenacil (protoporphyrinogen oxidase [PPO] inhibitors); acetochlor, S-metolachlor, dimethenamid-P, and pyroxasulfone (very long-chain fatty acid [VLCFA] inhibitors); and a nontreated control. Greenhouse bioassays were conducted using soil (depth, 0 to 10 cm) sampled at 0, 10, 20, 30, 40, and 50 d after treatment (DAT). Palmer amaranth and giant foxtail (weeds), and radish and cereal rye (cover crops) were used as bioindicators of herbicide levels in the soil. Bioassay results showed extended soil residual control of Palmer amaranth with sulfentrazone and pyroxasulfone; extended residual control of giant foxtail was observed with pyroxasulfone and S-metolachlor. Chlorimuron-ethyl and metribuzin were the most injurious herbicides to radish and cereal rye shortly after application, respectively, but minimal injury was observed from soil samples collected 50 DAT, indicating the use of PRE and fall-seeded cover crops in southern Wisconsin can be compatible. These results can support growers and practitioners with selection of effective PRE herbicides for Palmer amaranth and giant foxtail control and reduced impact on fall-seeded radish and cereal rye cover crops, altogether leading to more effective, diverse, and sustainable weed management programs.

Hair fescue is a common perennial grass that reduces yields in lowbush blueberry fields. This grass is suppressed with nonbearing-year foramsulfuron applications, though suppression may be improved through use of sequential glufosinate and foramsulfuron applications. The objective of this research was to determine the main and interactive effects of fall bearing-year glufosinate applications, spring nonbearing-year glufosinate applications, and spring nonbearing-year foramsulfuron applications on hair fescue. The experiment was a 2 by 2 by 2 factorial arrangement of fall bearing-year glufosinate application (0, 750 g ai ha–1), spring nonbearing-year glufosinate application (0, 750 g ai ha–1), and spring nonbearing-year foramsulfuron application (0, 35 g ai ha–1) arranged in a randomized complete block design at lowbush blueberry fields located in Parrsboro and Portapique, NS, Canada. Fall bearing-year glufosinate applications, spring nonbearing-year glufosinate applications, and spring nonbearing-year foramsulfuron applications alone provided inconsistent hair fescue suppression. Fall bearing-year glufosinate applications followed by spring nonbearing-year foramsulfuron applications, however, reduced nonbearing-year total tuft density, flowering-tuft density, and flowering-tuft inflorescence number at each site and reduced seed production at Portapique. Sequential fall bearing-year and spring nonbearing-year glufosinate applications or sequential spring nonbearing-year glufosinate and foramsulfuron applications reduced flowering-tuft density and flowering-tuft inflorescence number at each site but did not consistently reduce total tuft density. Sequential herbicide treatments reduced bearing-year seedling density and may therefore contribute to hair fescue seed bank management in lowbush blueberry.

Previous research has shown that glufosinate and nicosulfuron at low rates can cause yield loss to grain sorghum. However, research has not been conducted to pinpoint the growth stage at which these herbicides are most injurious to grain sorghum. Therefore, field tests were conducted in 2016 and 2017 to determine the most sensitive growth stage for grain sorghum exposure to both glufosinate and nicosulfuron. Field test were designed with factor A being the herbicide applied (glufosinate or nicosulfuron). Factor B consisted of timing of herbicide application including V3, V8, flagleaf, heading, and soft dough stages. Factor C was glufosinate or nicosulfuron rate where a proportional rate of 656 g ai ha−1 of glufosinate and 35 g ai ha−1 of nicosulfuron was applied at 1/10×, 1/50×, and 1/250×. Visible injury, crop canopy heights (cm), and yield were reported as a percent of the nontreated. At the V3 growth stage visible injury of 32% from the 1/10× rate of glufosinate and 51% from the 1/10× rate of nicosulfuron was observed. This injury was reduced by 4 wk after application (WAA) and no yield loss occurred. Nicosulfuron was more injurious than glufosinate at a 1/10× and 1/50× rate when applied at the V8 and flagleaf growth stages resulting in death of the shoot, reduced heading, and yield. Yield losses from the 1/10× rate of nicosulfuron were observed from V8 through early heading and ranged from 41% to 96%. Yield losses from the 1/50× rate of nicosulfuron were 14% to 16% at the flagleaf and V8 growth stages respectively. The 1/10× rate of glufosinate caused 36% visible injury 2 WAA when applied at the flagleaf stage, which resulted in a 16% yield reduction. By 4 WAA visible injury from either herbicide at less than the 1/10× rate was not greater than 4%. Results indicate that injury can occur, but yield losses are more probable from low rates of nicosulfuron at V8 and flagleaf growth stages.

Glyphosate and paraquat are effective preplant burndown herbicide options for multicrop vegetable production that uses plastic mulch, but problematic weeds such as wild radish, cutleaf evening primrose, annual morningglory, or horseweed may not be adequately controlled with these herbicides alone. The herbicides 2,4-D and dicamba could help control these troublesome weeds prior to planting if they can be removed from plastic mulch and thus avoid crop damage. Treatments included 2,4-D (1,065 and 2,130 g ae ha−1) and dicamba (560 and 1,120 g ae ha−1) applied broadcast over plastic mulch a day before transplanting. Just before transplanting, treatments received either 0.76 cm of water via overhead irrigation or no irrigation. Plastic mulch samples were collected at application and planting to determine herbicide presence using analytical techniques, and cantaloupe and zucchini squash were subsequently transplanted on the plastic beds. Analytical ultra-high performance liquid chromatography revealed that 88% to 99% of the initial herbicide concentration was present at crop planting when irrigation was not implemented. At most, a 1/50 rate of dicamba and a 1/500 rate of 2,4-D was present at planting when overhead irrigation was applied prior to transplanting. Maximum cantaloupe and squash injury from 2,4-D with irrigation was 10% and did not influence plant growth, biomass, or yield. For dicamba with overhead irrigation, cantaloupe injury was 35%, vine lengths were reduced by 24%, and maturity was delayed, whereas squash injury ranged from 9% to 12%, with no influence on growth or yield. Without irrigation to wash herbicides from the mulch prior to planting, 60% to 100% injury of both crops occurred with both herbicides. Zucchini squash was more tolerant to dicamba than cantaloupe. Results demonstrated that 2,4-D can be adequately removed from the surface of plastic mulch with irrigation, whereas a single irrigation event was not sufficient to remove dicamba.

The evolution of herbicide-resistant weeds has resulted in the necessity to integrate nonchemical control methods with chemicals for effective management in crop production systems. In soybean, control of the pigweed species, particularly herbicide-resistant waterhemp and Palmer amaranth, have become predominant concerns. Cereal rye planted as a winter cover crop can effectively suppress early-season weed emergence in soybean, including waterhemp, when planted at a rate of 123 kg ha−1. The objectives of this study were to determine the effects of different cereal rye seeding rates (0, 34, 56, 79, 110, and 123 kg ha−1) on early-season waterhemp suppression and soybean growth and yield. Soybean was planted into fall-seeded cereal rye, which was terminated within 4 d of soybean planting. The experiment was conducted over the 2018, 2019, and 2020 growing seasons in Columbia, Missouri. Effects of cereal rye on early-season waterhemp suppression varied by year and were most consistent at 56 kg ha−1 or higher seeding rates. Linear regression analysis of cereal rye biomass, height, or stand at soybean planting showed inverse relationships with waterhemp emergence. No adverse effects on soybean growth or yield were observed at any of the cereal rye seeding rates relative to plots that lacked cereal rye cover. Result differences among the years suggest that the successfulness of cereal rye on suppression of early-season waterhemp emergence is likely influenced by the amount of waterhemp seed present in the soil seed bank.

Glyphosate is the most widely used herbicide in the United States; however, concern is escalating about increasing residues of glyphosate and its metabolite aminomethylphosphonic acid (AMPA) in soil. There is a lack of scientific literature examining the response of cover crops to soil residues of glyphosate or AMPA. The objectives of this study were to evaluate the impact of glyphosate or AMPA residues in silty clay loam soil on emergence, growth, and biomass of cover crops, including cereal rye, crimson clover, field pea, hairy vetch, and winter wheat, as well as their germination in a 0.07% (0.7 g L–1) solution of AMPA or glyphosate. Greenhouse studies were conducted at the University of Nebraska–Lincoln to determine the dose response of broadleaf and grass cover crops to soil-applied glyphosate or AMPA. The results indicated that soil treated with glyphosate or AMPA up to 105 mg ae kg–1 of soil had no effect on the emergence, growth, above-ground biomass, and root biomass of any of the cover crop species tested. To evaluate the impact of AMPA or glyphosate on the seed germination of cover crop species, seeds were soaked in Petri plates filled with a 0.7 g L–1 solution of AMPA or glyphosate. There was no effect of AMPA on seed germination of any of the cover crop species tested. Seed germination of crimson clover and field pea in a 0.7 g L–1 solution of glyphosate was comparable to the nontreated control; however, the germination of cereal rye, hairy vetch, and winter wheat was reduced by 48%, 75%, and 66%, respectively, compared to the nontreated control. The results suggested that glyphosate or AMPA up to 105 mg ae kg–1 in silt clay loam soil is unlikely to cause any negative effect on the evaluated cover crop species.

Goosegrass control options in bermudagrass are limited. Topramezone is one option that offers excellent control of mature goosegrass, but application to bermudagrass results in unacceptable symptoms of bleaching and necrosis typical of hydroxyphenylpyruvate dioxygenase inhibitors. Previous research has shown that adding chelated iron reduced the phytotoxicity of topramezone without reducing the efficacy of the herbicide, resulting in safening when applied to bermudagrass. Our objective was to examine additional iron sources to determine whether similar safening effects occur with other sources. Field trials were conducted in the summers of 2016 to 2018 (Auburn University). Mixtures of topramezone and methylated seed oil were combined with six different commercial iron sources, including sodium ferric ethylenediamine di-o-hydroxyphenyl-acetate (FeEDDHA), ferrous diethylenetriamine pentaacetic acid (FeDTPA), iron citrate, FeSO4, and a combination of iron oxide/sucrate/sulfate, some of which contained nitrogen. Bermudagrass necrosis and bleaching symptoms were visually rated on a 0% to 100% scale. Reflectance (normalized difference vegetation index) and clipping yield measurements were also collected. Application of FeDTPA and FeSO4 reduced symptoms of bleaching and necrosis when applied with topramezone. Other treatments that contained nitrogen did not reduce injury but did reduce bermudagrass recovery time following the appearance of necrosis. Inclusion of small amounts of nitrogen often negated the safening effects of FeSO4. The iron oxide/sucrate/sulfate product had no effect on bleaching or necrosis. Data suggest that the iron source had a differential effect on bleaching and necrosis reduction when applied in combination with topramezone to bermudagrass. Overall, FeSO4 and FeDTPA safened topramezone the most on bermudagrass.

Field studies were conducted from 2005 to 2009 in Idaho and Oregon to 1) evaluate the competitive effect of volunteer potato on sugar beet yield (volunteer potato competition experiment), and 2) determine the optimum timing of volunteer potato removal from glyphosate-tolerant sugar beet fields using glyphosate (volunteer potato removal timing experiment). The volunteer potato competition experiment consisted of eight potato densities, including the untreated check: 0, 6,741, 10,092, 13,455, 16,818, 20,184, 26,910, and 40,365 tubers ha−1. The volunteer potato removal experiment consisted of 10 removal timings (including the untreated check) ranging from the 10-cm rosette stage to mid-tuber bulking. There was a linear decrease in sugar beet root and sucrose yield as volunteer potato density increased (P < 0.001) such that with every volunteer potato tuber per square meter, sugar beet root yield decreased by 15% and sucrose yield decreased by 14%. At the highest volunteer potato density (40,365 tubers ha−1), sugar beet root yield was 29,600 kg ha−1 (compared to 73,600 kg ha−1 for the untreated), representing a 60% reduction in sugar beet root yield. In the removal timing study, a one-time application of glyphosate at the 10-cm rosette, hooking, and tuber initiation stages provided 74% to 98% reduction in volunteer potato tuber biomass. Delaying volunteer potato removal beyond the tuber initiation stage reduced sugar beet root and sucrose yield (12% to 20%), resulting in an economic loss of $104 to $161 per hectare. The best potato removal timing that optimizes the trade-off between improved control and potential for sugar beet yield reductions is before or at the tuber initiation stage.

Chaff lining and chaff tramlining are harvest weed seed control (HWSC) systems that involve the concentration of chaff material containing weed seed into narrow (20 to 30 cm) rows between or on the harvester wheel tracks during harvest. These lines of chaff are left intact in the fields through subsequent cropping seasons in the assumption that the chaff environment is unfavorable for weed seed survival. The chaff row environment effect on weed seed survival was examined in field studies, and chaff response studies determined the influence of increasing amounts of chaff on weed seedling emergence. The objectives of these studies were to determine the influences of (1) chaff lines on the summer–autumn seed survival of selected weed species and (2) chaff type and amount on rigid ryegrass seedling emergence. There was frequently no difference (P > 0.05) in seed survival of four weed species (rigid ryegrass, wild oat, annual sowthistle, and turnip weed) when seeds were placed beneath or beside chaff lines. In one instance, wild oat seed survival was increased (P < 0.05) when seed were placed beneath compared to beside a chaff line. The pot studies determined that increasing amounts of chaff consistently resulted in decreasing numbers of rigid ryegrass seedlings emerging through chaff material. The suppression of emergence broadly followed a linear relationship in which there was approximately a 2.0% reduction in emergence with every 1,000 kg ha–1 increase in chaff material. This relationship was consistent across wheat, barley, canola, and lupin chaff types, indicating that the physical presence of the chaff was more important than chaff type. These studies suggested that chaff lines may not affect the survival over summer–autumn of the contained weed seeds but that the subsequent emergence of weed seedlings will be restricted by high amounts of chaff (>40,000 kg ha–1).

With the increasing focus on herbicide-resistant weeds and the lack of introduction of new modes of action, many producers have turned to planting annual cover crops as a method for reducing weed populations. Recent studies have suggested that perennial cover crops such as white clover could be used as living mulch. However, white clover is slow to establish and is susceptible to competition from winter weeds. Therefore, the objective of this study was to determine clover tolerance and weed control in established stands of white clover to several herbicides. Studies were conducted in the fall and winter of 2018 to 2019, and 2019 to 2020, at the J. Phil Campbell Research and Education Center in Watkinsville, GA, and the Southeast Georgia Research and Education Center in Midville, GA. POST applications of imazethapyr, bentazon, or flumetsulam at low and high rates, or in combination with 2,4-D and 2,4-DB, were applied when clover reached the 2- to 3-trifoliate stage. Six weeks after the initial POST application, a sequential application of bentazon and flumetsulam individually, and combinations of 2,4-D, 2,4-DB, and flumetsulam, were applied over designated plots. Clover biomass was similar across all treatments except where it was reduced by sequential applications of 2,4-D + 2,4-DB + flumetsulam in the 2019 to 2020 season, indicating that most treatments were safe for use on establishing living mulch clover. A single application of flumetsulam at the low rate or a single application of 2,4-D + 2,4-DB provided the greatest control of all weed species while minimizing clover injury compared with the nontreated check. These herbicide options allow for control of problematic winter weeds during clover establishment, thereby maximizing clover biomass and limiting canopy gaps that would allow summer weed emergence.

Rush skeletonweed is an invasive weed in winter wheat (WW)/summer fallow (SF) rotations in the low to intermediate rainfall areas of the inland Pacific Northwest. Standard weed control practices are not effective, resulting in additional SF tillage or herbicide applications. The objective of this field research was to identify herbicide treatments that control rush skeletonweed during the SF phase of the WW/SF rotation. Trials were conducted near LaCrosse, WA, in 2017–2019 and 2018–2020, and near Hay, WA, in 2018–2020. The LaCrosse 2017–2019 trial was in tilled SF; the other two trials were in no-till SF. Fall postharvest applications in October included clopyralid, clopyralid plus 2,4-D, clopyralid plus 2,4-D plus chlorsulfuron plus metsulfuron, aminopyralid, picloram, and glyphosate plus 2,4-D. Spring treatments of clopyralid, aminopyralid, and glyphosate were applied to rush skeletonweed rosettes. Summer treatments of 2,4-D were applied when rush skeletonweed initiated bolting. Plant density was monitored through the SF phase in all plots. Picloram provided complete control of rush skeletonweed through June at all three locations. Fall-applied clopyralid, clopyralid plus 2,4-D, and clopyralid followed by 2,4-D in summer reduced rush skeletonweed through June at the two LaCrosse sites but were ineffective at Hay. In August, just prior to WW seeding, the greatest reductions in rush skeletonweed density were achieved with picloram and fall-applied clopyralid at the two LaCrosse sites. No treatments provided effective control into August at Hay. Wheat yield in the next crop compared to the nontreated control was reduced only at one LaCrosse site by a spring-applied aminopyralid treatment, otherwise no other reductions were found. Long-term control of rush skeletonweed in WW/SF may be achieved by a combination of fall application of picloram, after wheat harvest, followed by an effective burn-down treatment in August prior to WW seeding.

Living mulches are cover crops grown simultaneously with and in close proximity to cash crops. Advantages of living mulches over dead cover crops may include increased weed suppression, reduced erosion and leaching, better soil health, and greater resource-use efficiency. Advantages of living mulches over synthetic mulches may include enhanced agroecosystem biodiversity and suitability for a wider range of cropping systems. A major disadvantage of this practice is the potential for competition between living mulches and cash crops. The intensity and outcome of mulch-crop competition depend on agroecosystem management as well as climate and other factors. In this review, we consider the management of living mulches for weed control in field and vegetable cropping systems of temperate environments. More than 50 yr of research have demonstrated that mechanical or chemical suppression of a living mulch can limit mulch-crop competition without killing the mulch and thereby losing its benefits. Such tactics can also contribute to weed suppression. Mechanical and chemical regulation should be combined with cultural practices that give the main crop a competitive advantage over the living mulch, which, in turn, outcompetes the weeds. Promising approaches include crop and mulch cultivar selection; changes to planting time, density, and planting pattern; and changes to fertilization or irrigation regimes. A systems approach to living mulch management, including an increased emphasis on the interactions between management methods, may increase the benefits and lower the risks associated with this practice.