Studies were conducted in 2019 and 2020 in Lewiston, NC, to determine the crop response of 4-hydroxyphenylpyrivate dioxygenase (HPPD)-resistant cotton to isoxaflutole (IFT) and other cotton herbicides as part of a cotton weed management program that included herbicides applied preemergence, early postemergence (EPOST), and mid-postemergence (MPOST). IFT was applied PRE at 105 g ha−1 alone and in various combinations with acetochlor, diuron, fluometuron, fluridone, fomesafen, pendimethalin, and pyrithiobac. EPOST treatments included IFT at 53 or 105 g ha−1 alone or in combination with glyphosate or glufosinate, or dimethenamid-P + glufosinate. Glyphosate + glufosinate was applied MPOST to all treatments except the nontreated control. Cotton injury from IFT applied PRE was minimal (0% to 3%). Injury following EPOST application of dimethenamid-P + glufosinate ranged from 3% to 5% and 6% to 9% in 2019 and 2020, respectively. In both years, injury from IFT applied PRE followed by IFT applied EPOST never exceeded injury from IFT applied PRE followed by dimethenamid-P + glufosinate. Isoxaflutole applied PRE followed by IFT applied EPOST at 105 g ha−1 resulted in 0% to 2% cotton injury, indicating that IFT can be applied either PRE or EPOST with minimal risk to cotton. Late-season cotton height and cotton lint yield were not affected by any herbicide treatment. The experimental HPPD-resistant cotton cultivar was minimally injured by IFT applied PRE and EPOST, it tolerated standard cotton herbicides, and yield loss was not observed. Given these results, HPPD-resistant cotton and IFT may be integrated into cotton weed management systems with minimal risk for cotton injury and provide an additional effective mechanism of action for managing troublesome weeds in cotton.

A non-GMO trait called Inzen™ was recently commercialized in grain sorghum to combat weedy grasses, allowing the use of nicosulfuron POST in the crop. Inzen™ grain sorghum carries a double mutation in the acetolactate synthase (ALS) gene Val560Ile and Trp574Leu, which potentially results in cross-resistance to a wide assortment of ALS-inhibiting herbicides. To evaluate the scope of cross-resistance to Weed Science Society of America Group 2 herbicides in addition to nicosulfuron, tests were conducted in 2016 and 2017 at the Lon Mann Cotton Research Station near Marianna, AR, the Arkansas Agricultural Research and Extension Center in Fayetteville, AR, and in 2016 at the Pine Tree Research Station near Colt, AR. The tests included ALS-inhibiting herbicides from all five families: sulfonylureas, imidazolinones, pyrimidinylthiobenzoics, triazolinones, and triazolopyrimidines. Treatments were made PRE or POST to grain sorghum at a 1× rate for crops in which each herbicide is labeled. Grain sorghum planted in the PRE trial were Inzen™ and a conventional cultivar. Visible estimates of injury and sorghum heights were recorded at 2 and 4 wk after herbicide application, and yield data were collected at crop maturity. In the PRE trial, no visible injury, sorghum height reduction, or yield loss were observed in plots containing the Inzen™ cultivar. Applications made POST to the Inzen™ grain sorghum caused visible injury, sorghum height reduction, and yield loss of 20%, 13%, and 35%, respectively, only in plots where bispyribac-Na was applied. There was no impact on the crop from other POST-applied ALS-inhibiting herbicides. These results demonstrate that the Inzen™ trait confers cross-resistance to most ALS-inhibiting herbicides and could offer promising new alternatives for weed control and protection from carryover of residual ALS-inhibiting herbicides in grain sorghum.

We conducted a survey in the major row-crop production regions of Texas to determine the response of waterhemp to glyphosate (5-enolpyruvylshikimate-3-phosphate synthase [EPSPS] inhibitor), atrazine (photosystem II [PSII] inhibitor), pyrithiobac (acetolactate synthase [ALS] inhibitor), tembotrione (hydroxyphenylpyruvate dioxygenase [HPPD] inhibitor), fomesafen (protoporphyrinogen oxidase [PPO] inhibitor), and dicamba (synthetic auxin). We evaluated 127 accessions for these herbicides. Resistance was confirmed on the basis of plant survival within an accession, and the injury ratings of surviving plants were used to categorize each accession as resistant (<50% injury) or less sensitive (50% to 89% injury). For glyphosate, approximately 27% of all tested accessions were resistant and 20% were less sensitive. The Gulf Coast region had the most glyphosate-resistant accessions (46% of the accessions from this region), followed by the Blacklands region (9%). A dose-response assay of the most resistant waterhemp accession (TX-25) exhibited 17-fold resistance to glyphosate when compared with a susceptible standard. Waterhemp resistance to atrazine also was common in the Gulf Coast region. The accession with the greatest atrazine resistance (TX-31) exhibited 47- and 68-fold resistance to this herbicide when applied POST and PRE, respectively. Widespread resistance to pyrithiobac was observed in waterhemp accessions throughout the Blacklands and Gulf Coast regions. The most resistant accession identified in this study was 61-fold resistant compared with a susceptible standard. No high-level resistance was detected for tembotrione, dicamba, or fomesafen, but high variability in sensitivity to tembotrione and dicamba was observed. One waterhemp accession exhibited reduced sensitivity to fomesafen; the rest were sensitive. Overall, at least two accessions exhibited resistance or reduced sensitivity to herbicides with five different sites of action. The study illustrates the prevalence of multiple herbicide resistance in waterhemp accessions in Texas and emphasizes the need to implement diversified management tactics.

A state-level survey was conducted across major row-crop production regions of Texas to document the level of sensitivity of Palmer amaranth to glyphosate, atrazine, pyrithiobac, tembotrione, fomesafen, and dicamba. Between 137 and 161 Palmer amaranth populations were evaluated for sensitivity to the labelled field rate (1X), and rated as resistant (≤49% injury), less sensitive (50% to 89% injury), or susceptible (90% to 100% injury). For glyphosate, 62%, 19%, 13%, and 13% of the populations from the High Plains, Central Texas, Rio Grande Valley, and Lower Gulf Coast, respectively, were resistant. Resistance to atrazine was more common in Palmer amaranth populations from the High Plains than in other regions, with 16% of the populations resistant and 22% less sensitive. Approximately 90% of the populations from the High Plains that exhibited resistance to atrazine POST also were resistant to atrazine PRE. Of the 160 populations tested for pyrithiobac, approximately 99% were resistant or less sensitive, regardless of the region. No resistance was found to fomesafen, tembotrione, or dicamba. However, 22% of the populations from the High Plains were less sensitive to 1X (93 g ai ha−1) tembotrione, but were killed at 2X, illustrating the background variability in sensitivity to this herbicide. For dicamba, three populations, all from the High Plains, exhibited less sensitivity at the 1X rate (controlled at the 2X rate; 1X = 560 g ae ha−1). One population exhibited multiple resistance to three herbicides with distinct sites of action (SOAs) involving acetolactate synthase, 5-enolpyruvylshikimate-3-phosphate synthase, and photosystem II inhibitors. Palmer amaranth populations exhibited less sensitivity to approximately 15 combinations of herbicides involving up to five SOAs. Dose-response assays conducted on the populations most resistant to glyphosate, pyrithiobac, or atrazine indicated they were 30-, 32-, or 49-fold or more resistant to these herbicides, respectively, compared with a susceptible standard.

Research was conducted to evaluate the sensitivity of cover crops to a low rate of soil-applied herbicides and investigate the likelihood of herbicide carryover to fall-seeded cover crops following an irrigated corn crop. In the sensitivity study, herbicides were applied at a 1/16×rate (to simulate four half-lives) 1 d after cover crop planting, whereas for the carryover study residual herbicides were applied at a 2×rate at the maximum label corn height or growth stage and cover crops sown immediately after corn harvest. In the sensitivity experiment, atrazine, diuron, fluridone, fomesafen, metribuzin, pyrithiobac, and sulfentrazone reduced emergence of the leguminous cover crops Austrian winterpea, crimson clover, and hairy vetch. However, reduced biomass production of leguminous cover crops in the spring was only observed for atrazine, fluridone, and pyrithiobac. For rapeseed, atrazine, flumioxazin, fluridone, pyrithiobac, pyroxasulfone, sulfentrazone, and tembotrione reduced emergence, but biomass production was reduced only by atrazine and fluridone. Conversely, wheat, cereal rye, barley, oats, and triticale were not affected by soil-applied herbicides. Barley was the only cereal cover crop that showed biomass reduction due to the application of flumioxazin, fluridone, mesotrione, S-metalochlor, and sulfentrazone. In the carryover study, with the exception of crimson clover, Austrian winterpea, cereal rye, hairy vetch, rapeseed, and wheat showed no negative affect on biomass production following a 2×rate of postemergence-applied residual herbicide in corn.

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

Variability in weed control following pyrithiobac applications has been observed under field conditions. The influence of temperature on this variability was investigated. Results from field studies performed over two growing seasons identified plant and air temperatures at the time of herbicide treatment that correlated with whole-plant efficacy differences. Based on the field data, weed control with pyrithiobac was acceptable at application temperatures of 20 to 34 C. To investigate a potential source of thermal limitations on pyrithiobac efficacy, the thermal dependence of in vitro inhibition of acetolactate synthase (ALS), the site of action for pyrithiobac, was examined. A crude leaf extract of ALS was obtained from Amaranthus palmeri. Relative inhibitor potency (I50) values were obtained at saturating substrate conditions for temperatures from 10 to 50 C. Regression analysis of field activity against I50 values showed the two data sets to be highly correlated (R 2 = 0.88). The thermal dependence of enzyme/herbicide interactions may provide another means of understanding environmental factors limiting herbicidal efficacy and predicting herbicide inhibition at the whole-plant level.

Experiments were conducted in 1993 and 1994 to determine persistence of pyrithiobac as determined by bioavailability following different application times in a silty clay. Pyrithiobac was applied at PPI, PRE, pinhead square (PHS), and first bloom (FB) application timings. Greenhouse studies were also conducted in 1993 and 1994 to determine pyrithiobac persistence under controlled conditions on a sandy loam soil. Slope comparison indicated no difference in degradation patterns in the field for any application timing of pyrithiobac within years; thus, application timings were combined for 1993 and 1994. Slope comparison also indicated no difference in slope between 1993 and 1994; thus, years were combined to determine pyrithiobac persistence. The initial concentration was 30 ηg g−1. The half-life of pyrithiobac was 62 d in the field. Analysis of covariance indicated no difference in slope for the 1993 and 1994 greenhouse studies, and years were combined to determine the half-life. The initial concentration was 43 η g−1. The half-life was 43 d in the greenhouse study.

In vitro acetolactate synthase (ALS) activity from three commercial imidazolinone-resistant corn hybrids (ICI 8692 IT, Pioneer 3751 IR, and Ciba 4393 IMR) was compared to imidazolinone-sensitive isogenic hybrid controls for sensitivity to 11 herbicides representing four classes of ALS-inhibiting herbicide chemistry. Acetolactate synthase activity from Pioneer IR and Ciba IMR was cross-resistant to all four classes of ALS inhibitors, ranging from 48- to 5,000-fold. The ICI IT hybrid displayed only four- to eightfold resistance to the six imidazolinone herbicides and the pyrimidinylthiobenzoate herbicide, pyrithiobac, but no cross-resistance to the sulfonylurea and triazolopyrimidine sulfonanilide herbicides. The four- to eightfold enzyme resistance to imidazolinone herbicides provides whole-plant resistance; however, the sevenfold enzyme resistance to pyrithiobac was insufficient to afford whole-plant protection to a field application rate of the herbicide. A second imidazolinone-specific resistance allele, XI-12, currently under commercial development, was examined for the level of dominance at the enzyme level. In the heterozygous state, imazethapyr resistance was fivefold, compared to 250-fold in the homozygous condition, indicating XI-12 is a semidominant trait. No cross-resistance to nicosulfuron or primisulfuron was observed in the heterozygous XI-12 hybrid extracts nor to nicosulfuron in the XI-12 homozygote; however, a fivefold resistance to primisulfuron was detected in the XI-12 homozygote.

Following six consecutive annual applications of imazaquin in combination with trifluralin or pendimethalin to several soybean fields on the Delmarva Peninsula, unacceptable smooth pigweed control was observed. Field and greenhouse studies were conducted to determine if this population of smooth pigweed was resistant to imazaquin and other herbicides. In field research, imazaquin and imazethapyr gave complete control of the susceptible (S) population while providing no control of the resistant (R) population; pyrithiobac controlled 99 and 90% of the R and S populations, respectively. Pendimethalin, metribuzin, MON-12000, and flumiclorac gave less than 75% control of both S and R populations. Chlorimuron, primisulfuron, CGA-152005, and lactofen gave above 75% control, and thifensulfuron and nicosulfuron gave above 90% control of both S and R populations. Seeds were collected from the R and S smooth pigweed populations for research in the greenhouse. Greenhouse studies confirmed high levels of resistance to imazaquin and imazethapyr and low levels of cross-resistance to rimsulfuron and chlorimuron in the R population. Susceptibility of the R population to nicosulfuron, thifensulfuron, pyrithiobac, and pendimethalin was comparable to that of the S population.

Field experiments were established to evaluate coffee senna control in cotton with registered PRE, early POST-directed (EPD), and late POST-directed (LPD) herbicides and with pyrithiobac applied PRE and early POST. Fluometuron and norflurazon applied PRE controlled coffee senna 87 and 65%, respectively, 6 wk after planting (WAP). Methazole applied EPD controlled coffee senna 96% 2 wk after application, whereas fluometuron and MSMA applied EPD controlled 70 and 16%, respectively. LPD applications of cyanazine, diuron, and prometryn averaged only 45% control 8 WAP. MSMA applied LPD controlled coffee senna only 12%. Fluometuron and norflurazon applied PRE followed by methazole applied EPD and cyanazine applied LPD controlled coffee senna 98 and 99% 6 WAP, respectively. PRE, early POST, and PRE followed by early POST applications of pyrithiobac controlled coffee senna 88, 89, and 95% 6 WAP, respectively. Seed cotton yields were similar to weed-free cotton with all treatments except MSMA applied EPD and the LPD treatments, all of which provided unacceptable (12 to 49%) control 8 WAP.

Experiments were conducted to evaluate PRE and POST cotton herbicides for control of MSMA-resistant (R) and -susceptible (S) common cocklebur biotypes, and to determine potential cross-resistance of the R biotype to other arsenical and membrane disruptor herbicides. Cyanazine and clomazone applied PRE were the most effective herbicides for control of R populations. Lactofen or cyanazine in combination with MSMA controlled R and S biotypes better than fluometuron or pyrithiobac combined with MSMA. MSMA-resistant common cocklebur was not cross-resistant to other arsenical herbicides. Significant differences in cellular electrolyte leakage and chlorophyll content of the treated leaf between biotypes were not evident for paraquat, acifluorfen, and MSMA.

Seeds were collected from an imidazolinone-resistant (R) population of smooth pigweed near Marion, MD, and from an imidazolinone-susceptible (S) population near Painter, VA, and grown in the greenhouse. Acetolactate synthase (ALS) enzyme was extracted from both biotypes and assayed in the presence of CGA 152005, chlorimuron, halosulfuron, imazaquin, imazethapyr, nicosulfuron, primisulfuron, pyrithiobac, rimsulfuron, and thifensulfuron to determine if an altered ALS was the mechanism of resistance in the R biotype and to determine if this biotype was cross-resistant to other ALS inhibitor herbicides. The inhibitor concentration required to cause a 50% reduction in ALS activity (I50) was calculated for each herbicide. ALS from the R biotype was approximately 71-, 109,000-, and 9-fold more resistant to imazaquin, imazethapyr, and rimsulfuron, respectively, than that from the S biotype. ALS from the R biotype was approximately threefold more sensitive to pyrithiobac and thifensulfuron than that from the S biotype. R ALS was also slightly more tolerant to CGA 152005 and nicosulfuron and slightly more sensitive to primisulfuron and chlorimuron. ALS from both biotypes generally responded similarly to halosulfuron. Resistance in the R biotype was due to an altered form of ALS that is insensitive to the imidazolinone herbicides and rimsulfuron.

Efficacy of several acetolactate synthase (ALS)-inhibiting herbicides was evaluated for yellow nutsedge control over a 3-yr period on a State sandy loam and in the greenhouse. Herbicides were applied POST to yellow nutsedge at actual or anticipated commercial rates. Yellow nutsedge control was above 77% from MON 12000 and chlorimuron. Control ranged from 41 to 89% from primisulfuron, pyrithiobac, and rimsulfuron. Control from nicosulfuron and imazethapyr was 58% or less while thifensulfuron and CGA-152005 had almost no activity on yellow nutsedge. In greenhouse studies, MON 12000 controlled yellow nutsedge better than did chlorimuron, and imazethapyr gave better control than in the field.

In 2005, the existence of glyphosate-resistance in Palmer amaranth was confirmed at a single 250 ha field site in Macon County, Georgia. Currently, all cotton producing counties in Georgia are infested, to some degree, with glyphosate-resistant Palmer amaranth. In 2010 and 2011, surveys were administered to Georgia growers and extension agents to determine how the development of glyphosate-resistance has affected weed management in cotton. According to respondents, the numbers of cotton acres that were treated with paraquat, glufosinate and residual herbicides effective against Palmer amaranth more than doubled between 2000 to 2005 and 2006 to 2010. Glyphosate use declined between 2000 to 2005 and 2006 to 2010 although, on average, the active ingredient was still applied to a majority of cotton acres. Although grower herbicide input costs have more than doubled following the evolution and spread of glyphosate resistance, chemically-based control of Palmer amaranth is still not adequate. As a consequence, Georgia cotton growers hand weeded 52% of the crop at an average cost of $57 per hand-weeded ha; this represents a cost increase of at least 475% as compared to the years prior to resistance. In addition to increased herbicide use and hand weeding, growers in Georgia are also using mechanical, in-crop cultivation (44% of acres), tillage for the incorporation of preplant herbicides (20% of the acres), and post-harvest deep-turning (19% of the acres every three years) for weed control. Current weed management systems are more diverse, complex and expensive than those employed only a decade ago, but are effective at controlling glyphosate-resistant Palmer amaranth in glyphosate-resistant cotton. The success of these programs may be related to producers improved knowledge about herbicide resistance, and the biological attributes that make Palmer amaranth so challenging, as well as their ability to implement their management programs in a timely manner.

Soybean is a major crop cultivated in Brazil, and acetolactate synthase (ALS)-inhibiting herbicides are widely used to control weeds in this crop. The continuous use of these ALS-inhibiting herbicides has led to the evolution of herbicide-resistant weeds worldwide. Greater beggarticks is a polyploid species and one of the most troublesome weeds in soybean production since the discovery of ALS-resistant biotypes in 1996. To confirm and characterize the resistance of greater beggarticks to ALS inhibitors, whole-plant bioassays and enzyme experiments were conducted. To investigate the molecular basis of resistance in greater beggarticks the ALS gene was sequenced and compared between susceptible and resistant biotypes. Our results confirmed that greater beggarticks is resistant to ALS inhibitors and also indicated it possesses at least three isoforms of the ALS gene. Analysis of the nucleotide and deduced amino acid sequences among the isoforms and between the biotypes indicated that a single point mutation, G–T, in one ALS isoform from the resistant biotype resulted in an amino acid substitution, Trp574Leu. Two additional substitutions were observed, Phe116Leu and Phe149Ser, in a second isoform of the resistant biotype, which were not yet reported in any other herbicide-resistant ALS gene; thus, their role in conferring herbicide resistance is not yet ascertained. This is the first report of ALS mutations in an important, herbicide-resistant weed species from Brazil.

Cotton growers rely heavily upon glufosinate and various residual herbicides applied preplant, PRE, and POST to control Palmer amaranth resistant to glyphosate and acetolactate synthase-inhibiting herbicides. Recently deregulated in the United States, cotton resistant to dicamba, glufosinate, and glyphosate (B2XF cotton) offers a new platform for controlling herbicide-resistant Palmer amaranth. A field experiment was conducted in North Carolina and Georgia to determine B2XF cotton tolerance to dicamba, glufosinate, and glyphosate and to compare Palmer amaranth control by dicamba to a currently used, nondicamba program in both glufosinate- and glyphosate-based systems. Treatments consisted of glyphosate or glufosinate applied early POST (EPOST) and mid-POST (MPOST) in a factorial arrangement of treatments with seven dicamba options (no dicamba, PRE, EPOST, MPOST, PRE followed by [fb] EPOST, PRE fb MPOST, and EPOST fb MPOST) and a nondicamba standard. The nondicamba standard consisted of fomesafen PRE, pyrithiobac EPOST, and acetochlor MPOST. Dicamba caused no injury when applied PRE and only minor, transient injury when applied POST. At time of EPOST application, Palmer amaranth control by dicamba or fomesafen applied PRE, in combination with acetochlor, was similar and 13 to 17% greater than acetochlor alone. Dicamba was generally more effective on Palmer amaranth applied POST rather than PRE, and two applications were usually more effective than one. In glyphosate-based systems, greater Palmer amaranth control and cotton yield were obtained with dicamba applied EPOST, MPOST, or EPOST fb MPOST compared with the standard herbicides in North Carolina. In contrast, dicamba was no more effective than the standard herbicides in the glufosinate-based systems. In Georgia, dicamba was as effective as the standard herbicides in a glyphosate-based system only when dicamba was applied EPOST fb MPOST. In glufosinate-based systems in Georgia, dicamba was as effective as standard herbicides only when dicamba was applied twice.

A field experiment was conducted over 2 yr to study efficacy of bromoxynil mixtures with pyrithiobac or MSMA applied postemergence (POST) with and without fluometuron or fluometuron plus pendimethalin preemergence (PRE) for control of broadleaf weeds in ultra narrow row bromoxynil-resistant cotton in the Mississippi Delta. Bromoxynil applied POST (single or sequential) provided variable control of common purslane (<9%), sicklepod (<35%), Palmer amaranth (<46%), prickly sida (>75%), hyssop spurge (>79%), hemp sesbania (>96%), and pitted morningglory (100%) at 4 wk after early POST (WAT). Broadleaf weed control increased when PRE herbicides were followed by bromoxynil or bromoxynil plus pyrithiobac or MSMA POST. Weed control generally decreased at harvest compared to 4 WAT, and the decrease was greater in bromoxynil POST-only programs compared to bromoxynil POST following PRE programs. Seed cotton yield with bromoxynil POST-only programs was lower (400 to 2,810 kg/ha) compared to bromoxynil POST programs following PRE herbicides (2,150 to 3,720 kg/ha). Early-season weed interference and variable control of weeds in bromoxynil POST-only programs resulted in greater cotton stand reduction and lower open bolls per plant compared to bromoxynil POST programs following PRE herbicides.

Greenhouse and field research evaluated yellow nutsedge growth, vegetative control, and tuber production after application of glyphosate, various acetolactase synthase (ALS)–inhibiting herbicides, and tank mixtures thereof. Yellow nutsedge was controlled by the herbicides halosulfuron at 35 g ai/ha, chlorimuron at 12 g ai/ha, and imazethapyr–imazapyr at 62 g ai/ha (> 70% control); imazethapyr at 70 g ai/ha, glyphosate at 840 g ae/ha, cloransulam at 17.5 g ai/ha, and rimsulfuron at 17.5 g ai/ha (40 to 70% control); and imazamox at 45 g ai/ha (< 40% control). Compared with the untreated control, tuber fresh weight in the field was reduced 45 to 91%, and tuber density was reduced 33 to 90% by all herbicide treatments 42 wk after treatment (WAT) except imazamox and rimsulfuron. Tuber sprouting was reduced to 19% in plots treated with halosulfuron and pyrithiobac compared with untreated yellow nutsedge 42 WAT. Chlorimuron and imazethapyr–imazapyr controlled yellow nutsedge at least 90%, prevented panicle formation, and reduced tuber density and fresh weight by 90% or more 14 WAT in the greenhouse. The addition of glyphosate to cloransulam or imazethapyr increased yellow nutsedge control and reduced tuber density and fresh weight when compared with either ALS-inhibiting herbicide or glyphosate applied alone. Tuber density data indicated that there were 8 tubers for every gram of tubers harvested. Yellow nutsedge height was 15 to 20 cm 4 to 5 wk after tillage, using growth analysis data. Long-term yellow nutsedge management may be aided with treatments that reduce tuber production.

Field studies were conducted in 2000 and 2001 at Rohwer, AR. Trifloxysulfuron (5.3 and 8 g ai/ha) and pyrithiobac (70 g ai/ha) were applied preemergence (PRE) and postemergence (POST) broadcast at the two- to three-leaf (EP) and three- to four-leaf (MP) cotton growth stages. Both materials were also applied POST in combination with glyphosate at 560 g ae/ha or bromoxynil at 560 g ai/ha at both growth stages. Trifloxysulfuron applied EP or MP at 8 g/ha provided greater control of sicklepod and pitted morningglory 28 d after application (DAA) than trifloxysulfuron at 5.3 g/ha or pyrithiobac at 70 g/ha; however, control of prickly sida was greater with pyrithiobac than with trifloxysulfuron at either rate. Glyphosate alone controlled sicklepod, prickly sida, and pitted morningglory greater than 80%. The addition of trifloxysulfuron at 8 g/ha and pyrithiobac at 70 g/ ha increased control of all species over glyphosate alone 28 DAA. Bromoxynil at 560 g/ha controlled pitted morningglory and hemp sesbania at all application timings; however, sicklepod and Palmer amaranth control was less than 50% with bromoxynil applied alone. When bromoxynil was applied in combination with trifloxysulfuron at either rate, control of sicklepod and Palmer amaranth increased to 80% or greater at all application timings. Trifloxysulfuron has the potential to complement both the glyphosate-resistant and bromoxynil-resistant weed control programs by providing control of less susceptible weeds and by providing residual control to both programs.