Experiments conducted for two consecutive years indicated that barnyardgrass, large crabgrass, and giant foxtail interfered with the growth and development of container-grown ‘Gold Drop’ bush cinquefoil. Grass weed densities ranging from one to six weeds per container reduced Gold Drop bush cinquefoil growth. Bush cinquefoil shoot dry weight, averaged over all grass weeds, was decreased as much as 75% after 83 days of interference. The reduction of cinquefoil growth was independent of the number of grass weeds in the container.

Imazethapyr at 0.05 to 0.14 kg ai/ha applied preplant incorporated, preemergence, and postemergence was evaluated alone and with complementary herbicides in the field for weed control in soybean. Imazethapyr controlled 90% or more smooth pigweed regardless of application method or herbicide rate. Imazethapyr at 0.05 kg/ha controlled jimsonweed 30% better postemergence compared to soil applications. Imazethapyr at 0.10 kg/ha controlled 90% or more velvetleaf regardless of application method. The addition of alachlor to soil-applied imazethapyr enhanced giant foxtail, jimsonweed, and velvetleaf control. Adding acifluorfen or bentazon to postemergence imazethapyr antagonized weed control. Adding sethoxydim to postemergence imazethapyr was not beneficial.

Weed control and corn vigor were evaluated to determine the effects of application rate, timing, and other POST herbicides on primisulfuron activity. Corn injury caused by primisulfuron was very low. Weed control varied with species and stage of growth. Primisulfuron showed high activity on emerged johnsongrass, particularly with early postemergence (EP) and mid postemergence (MP) applications. However, these treatments did not provide full season control of this species due to regrowth from rhizomes and continuous germination of new seeds. Primisulfuron controlled giant foxtail with the EP timing (< 5 cm weed height), but not with MP and late postemergence (LP) applications. Common lambsquarters and redroot pigweed control was most effective with EP applications. Primisulfuron in combination with cyanazine, atrazine, cyanazine plus tridiphane, atrazine plus tridiphane, bentazon, 2,4-D, dicamba, or paraquat controlled common lambsquarters and redroot pigweed better than primisulfuron applied alone. Johnsongrass control decreased when primisulfuron was combined with paraquat or 2,4-D and giant foxtail control decreased when primisulfuron was combined with 2,4-D or dicamba.

In greenhouse studies, the butyl ester of fluazifop {(±)-2-[4-[[5-(trifluoromethyl)-2-pyridinyl]oxy]phenoxy]propanoic acid} applied preemergence at 0.035 kg ai/ha gave 91% control of goosegrass (Eleusine indica Gaertn. ♯ ELEIN), 79% control of large crabgrass [Digitaria sanguinalis (L.) Scop. ♯ DIGSA], and 73% control of giant foxtail (Setaria faberi Herrm. ♯ SETFA). In field studies, the butyl ester of fluazifop at 0.56 kg ai/ha applied preemergence gave 79% control of goosegrass, 76% control of large crabgrass, and 53% control of giant foxtail. The butyl ester of fluazifop at 0.07 kg/ha gave 79 to 85% control of each grass at the pretillering stage in field studies. The same rate applied at the early tillering stage gave 84% control of goosegrass but only 53 and 58% control of large crabgrass and giant foxtail, respectively. Relative species response was similar from spray and leaf-spot applications of the herbicide. The butyl ester of fluazifop at 4 μg/plant when spot-applied to leaves of the three grasses at the tillering stage resulted in 65% control of goosegrass but only 20 and 25% control of large crabgrass and giant foxtail, respectively.

In 1985, when weed densities were low (169 plants/m2 in untreated control), imazaquin applied at 0.07 kg ai/ha early preplant controlled over 90% of all weeds before no-till planting of soybeans. In 1986 and 1987 when weed densities were higher (589 plants/m2 in untreated control), addition of 1.1 kg ai/ha or more of metolachlor to imazaquin (0.07 kg/ha) before soybean planting controlled 95% or more of the grass weeds and 83% or more of the broadleaf weeds. Imazaquin plus metolachlor applied less than 1 day after soybean planting controlled less than 70% of the emerged weeds in 1986 and 1987; common lambsquarters was most tolerant. Early preplant treatments controlled more weeds throughout the growing season than treatments applied after planting. Splitting herbicide treatments among application times generally did not increase weed control compared to single applications. Early preplant applications resulted in higher soybean densities and taller soybeans 30 days after planting in 1986 and 1987 than treatments applied after planting. Soybean yields increased as weed control increased. Weed control and soybean yields were greater with early preplant treatments than paraquat plus alachlor plus metribuzin applied preemergence in 1986 and 1987. No carryover of imazaquin residue was detected through corn bioassay in the field.

Giant foxtail (Setaria faberi Herrm. # SETFA) seed germination was about 55% in water but increased to >90% after pretreatment in polyethyleneglycol 8000 (PEG) at water potentials of −0.3 MPa or less. Pretreatment at 20 C required about 24 h exposure to PEG for maximum effect, but at 35 C shorter times (4 to 8 h) gave a partial effect. Treatment with PEG can begin at the time of seed wetting or after the seeds have imbibed water for 24 h. Continuous exposure to a water potential of −0.5 MPa PEG (or less) imhibited germination. Other methods of applying temporary water stress to the seeds, such as slow hydration in a humid atmosphere, or drying after partial hydration, increased germination in a manner similar to PEG treatment. The relatively slow response kinetics with PEG suggest that increased germination was caused by physiological adaptation to water stress, possibly by observed adjustments in seed water potential. It is suggested the water stress mechanism could operate under field conditions where wetting-drying cycles are common.

Season-long interference of shattercane, giant foxtail, common cocklebur, and common lambsquarters in corn was evaluated in the field at weed densities from 0.4 to 13.1 plants or clumps/m of corn row during 1985, 1986, and 1987. Corn seed yields decreased linearly with increases in the density of clumps of 2 to 3 shattercane plants and 5 to 8 giant foxtail plants, reaching 22% yield loss at 6.6 shattercane clumps/m of row and 18% yield loss at 13.1 giant foxtail clumps/m of row. Increases in common cocklebur density caused corn yields to decrease curvilinearly in 1985 with a maximum predicted yield loss of 27% occurring at a density of 4.7 common cocklebur plants/m of row. In 1986 and 1987, yields decreased linearly as common cocklebur density increased to 6.6 plants/m of row, where a 10% yield loss was observed. Common lambsquarters reduced corn yields only in 1985. In this year, yields decreased curvilinearly with increasing weed density, resulting in a maximum yield loss of 12% at 4.9 common lambsquarters plants/m of row. Corn yields averaged 11600 kg/ha when grown without weed interference in these experiments.

A reduced-till (RT) experiment determined the effect of rye seeding density and method of kill on rye biomass persistence, weed suppression, and tomato yield. ‘Wheeler’ rye was seeded at 56, 110, and 170 kg ha−1 in the fall of 1988 and 1989 in Champaign, IL; Lexington, KY; and Lafayette, IN. One wk before transplanting tomatoes, rye was desiccated either by applying glyphosate at 1.1 kg ha−1 and mowing (RT-glyphosate) or by mowing alone (RT-mowed). Both methods left rye residues on the soil surface as a mulch. Seeding density did not affect rye biomass, weed control, or tomato yield. Rye biomass differed depending on location and year, ranging from 320 to 1150 gm−2. Rye was completely killed by glyphosate, but regrew following mowing. RT-glyphosate suppressed weeds for 4 to 8 wk, which was similar to the suppression from conventional tillage (fall plowing with spring disking and harrowing) with trifluralin and metribuzin (CT-herbicide). Weed communities varied, but redroot pigweed and giant foxtail were present at all three locations. All treatments required supplemental weed management for commercially acceptable control. Except for IL in 1990, processing tomato yields (kg ha−1) in RT-glyphosate with hand-weeding were equal or better than yields in the CT treatments.

Tridiphane [2-(3,5-dichlorophenyl)-2-(2,2,2-trichloroethyl)oxirane] is a potent synergist of atrazine for postemergence control of weeds such as giant foxtail (Setaria faberi Herrm. ♯ SETFA) and large crabgrass [Digitaria sanguinalis (L.) Scop. ♯ DIGSA]. We determined whether: a) tridiphane could syngergize the activity of other herbicides known to be detoxified via enzymatic conjugation to glutathione, and b) differential toxicities of the synergized herbicides could provide control of proso millet (Panicum miliaceum L. ♯ PANMI) in corn (Zea mays L. “PAG SXIII”). Four herbicides were used in this study: EPTC (S-ethyl dipropylthiocarbamate), atrazine [2-chloro-4-(ethylamino)-6-(isopropylamino)-s-triazine], CDAA (N-N-diallyl-2-chloroacetamide), and alachlor [2-chloro-2’,6’-diethyl-N-(methoxymethyl) acetanilide]. Herbicides and herbicide-synergist combinations were applied postemergence. In corn, tridiphane synergized the activity of EPTC at 2 and 4 kg ai/ha, causing 22 to 25% growth reduction. Atrazine was ineffective and CDAA only slightly effective in combination with tridiphane in causing growth reduction. However, alachlor was markedly synergized by tridiphane at both 2 and 4 kg ai/ha, resulting in 36 to 54% growth reduction compared with plants treated with herbicides alone. Proso millet followed a similar trend to corn: EPTC and alachlor were effectively synergized by tridiphane, while atrazine and CDAA were ineffective. Importantly, however, the rates of herbicide used for proso millet control were much lower than those used for corn. Our data suggest that tridiphane used in combination with EPTC or alachlor could provide improved control of proso millet in corn.

Efficacy of primisulfuron and reduced rates of nicosulfuron on woolly cupgrass, wild-proso millet, and giant foxtail in field corn was evaluated in 1994 and 1995. Nicosulfuron was applied at 18, 27, and 36 g ai/ha alone and with 20 g ai/ha primisulfuron. Woolly cupgrass control from nicosulfuron at 18 and 27 g/ha was less than control from 36 g/ha (79% and 84% vs. 90%, respectively). Woolly cupgrass control was 5% greater when primisulfuron was combined with nicosulfuron at 27 and 36 g/ha than when nicosulfuron was applied alone. Corn grain yields were similar among all nicosulfuron plus primisulfuron treatments applied to control woolly cupgrass in 1994. In 1995, corn grain yield was increased 900 kg/ha when primisulfuron was combined with nicosulfuron at 18 g/ha compared to nicosulfuron applied at the same rate alone. Wild-proso millet control 3 WAT with nicosulfuron at 18 g/ha was less than control with nicosulfuron at 36 g/ha. Wild-proso millet control 8 WAT with nicosulfuron alone was greater than when nicosulfuron at any rate was applied with primisulfuron. No differences in corn grain yields were observed across nicosulfuron rates or combinations with primisulfuron to control wild-proso millet either year. Giant foxtail control and corn grain yield were not affected by nicosulfuron rate or combined applications of nicosulfuron and primisulfuron either year.

Greenhouse and field experiments were conducted to investigate degradation rates and efficacy of EPTC (S-ethyl dipropyl carbamothioate), butylate [S-ethyl bis(2-methylpropyl)carbamothioate], vernolate (S-propyl dipropylcarbamothioate), and cycloate (S-ethyl cyclohexylethylcarbamothioate) in soils with and without prior history of thiocarbamate use. Herbicide persistence was measured by an oat (Avena sativa L.) bioassay, and giant foxtail (Setaria faberi Herrm. # SETFA) control was visually estimated in field studies. Both greenhouse and field studies indicated that enhanced thiocarbamate degradation occurred when the same herbicide (EPTC, butylate, or vernolate) was applied over successive years. Addition of dietholate (O,O-diethyl O-phenyl phosphorothioate) or fonofos (O-ethyl-S-phenylethylphosphonodithioate) increased thiocarbamate persistence and giant foxtail control in soils with prior thiocarbamate exposure. Use of dietholate or fonofos two or three consecutive years with EPTC or butylate again resulted in enhanced degradation. EPTC persistence and giant foxtail control were not affected by prior treatments or tank mixes with carbofuran (2,3-dihydro-2,2-dimethyl-7-benzofuranyl methylcarbamate). Rotation away from successive applications of the same thiocarbamate herbicide (EPTC, butylate, or vernolate) improved herbicide efficacy.

Clomazone at 0.7 kg ai/ha or more, applied early preplant, completely controlled weeds before planting of no-till soybeans. Under low weed density (57 plants/m2 in untreated control) in 1985, grass weed control was nearly complete and not affected by clomazone application time. Late-season broadleaf weed control was less with preemergence application of clomazone at 1.1 or 1.4 kg/ha than with an early preplant or early preplant-preemergence split application of the same clomazone rate. Addition of metribuzin at 0.2 kg ai/ha overcame this control deficiency. Under greater weed densities (330 plants/m2 in untreated control) during 1986 and 1987, early preplant-preemergence split applications gave the greatest control of both grass and broadleaf weeds throughout the growing season. Preemergence application of clomazone failed to completely control common lambsquarters emerged at the time of application. Early preplant applications failed to maintain redroot pigweed control throughout the season. Differences in soybean yield were attributed to differences in weed control. No significant carryover of clomazone residue was detected through greenhouse or field bioassays.

Field experiments were conducted from 1979 to 1989 to determine the influence of conventional, reduced, and no-tillage systems and different herbicide combinations on weed species and population, weed control, and soybean injury, population, and yield. In no-till (NT) non-treated plots, there was an abrupt shift from horseweed as the dominant early spring emerging weed to gray goldenrod in 1985. Following its initial observation, gray goldenrod became the dominant species within 2 yr, with giant foxtail as the only other species observed in these plots. Giant foxtail was the dominant weed species from 1980 to 1989 in conventional till (CT) and reduced-till (RT) plots. There also was a shift in the frequency of occurrence and in density of several broadleaf weed species during the 11-yr study. Most herbicides provided excellent control of all weeds in all tillage systems, especially those that included POST herbicides. There was little difference between glyphosate and paraquat in controlling weeds present at the time of planting in NT. PRE herbicides caused 2 to 9% soybean injury with slightly greater injury occurring in CT and RT than in NT. The POST broadleaf herbicides did not significantly increase soybean injury. There were no differences in soybean population or yield among the herbicide treatments regardless of tillage. There also was no difference in soybean population or yield in NT compared with CT when averaged over all herbicide treatments.

Field studies were conducted in 1996 and 1997 at Belleville and Pawnee, IL, to evaluate single and sequential applications of glufosinate on tolerance of glufosinate-resistant corn and annual weed control. Glufosinate caused 0 to 13% corn injury 7 days after treatment (DAT) and 0 to 6% corn injury 28 DAT. Injury was characterized as stunting with glufosinate. Glufosinate at 400 to 1,200 g ai/ha did not reduce final corn height or grain yield. At Pawnee in both years and at Belleville in 1996, a single application of glufosinate at 400 g/ha controlled giant foxtail, velvetleaf, ivyleaf morningglory, and common lambsquarters 85 to 100%. At Belleville in 1997, sequential applications of glufosinate provided greater weed control (87 to 100%) than a single application (0 to 63%) because of weed emergence after application. Weed control with a single application of glufosinate or with nicosulfuron plus bromoxynil was similar at both locations. Height and grain yield of glufosinate-resistant corn were not different from that of glufosinate-susceptible corn (isoline of glufosinate-resistant corn).

The effect of tillage systems on depth of emergence and densities of giant and green foxtail under different environmental and cropping conditions were evaluated from 1985 to 1987 at Arlington, Hancock, and Janesville, WI. Mean emergence depths in no-till were the shallowest, followed by chisel plow and conventional tillage at each location. At least 40% of the giant and green foxtail plants emerged from the upper 1 cm of soil in no-till compared to about 25% in chisel plow and less than 15% in conventional tillage. As many as 25% of the plants emerged from greater than 4 cm in conventional tillage compared to about 10% in chisel plow and less than 5% in no-till. Seedlings emerged from greater depths in a loamy sand than in a silt loam soil regardless of tillage system. At Arlington, green foxtail was the dominant species in conventional tillage, while giant foxtail dominated in chisel plow and no-till. Foxtail densities were greater in chisel plow and no-till than in conventional tillage at all three locations.

Application time did not greatly influence control of velvetleaf (Abutilon theophrasti Medik. # ABUTH) or common lambsquarters (Chenopodium album L. # CHEAL) in no-till corn (Zea mays L. ‘Pioneer 3747’) with fluorochloridone {3-chloro-4-(chloromethyl)-1-[3-(trifluoromethyl) phenyl]-2-pyrrolidinone}. Giant foxtail (Setaria faberi Herrm. # SETFA) control was reduced as much as 25% by 90 days after planting when fluorochloridone was applied early preplant rather than preemergence. Fluorochloridone at 0.8 kg/ha applied preplant or preemergence gave 83% or greater control of common lambsquarters and giant foxtail for the entire growing season. However, velvetleaf control with the same treatments was 61% or less. Fluorochloridone caused minimal corn injury. Greenhouse bioassay indicated that fluorochloridone may carry over and injure soybean [Glycine max (L.) Merr.] the year after application. Imbibition of fluorochloridone by seed of corn and giant foxtail did not reduce germination at concentrations up to 10-3 M. Giant foxtail seedling fresh weight was reduced 80% following imbibition of 10-5 M fluorochloridone. Corn seedling fresh weight was not reduced by imbibition of up to 10-4 M fluorochloridone.

Greenhouse and laboratory studies were conducted to determine the effect of 22 postemergence corn broadleaf herbicide combinations on the efficacy of sethoxydim applied to giant foxtail, large crabgrass, and shattercane. Eighteen combinations caused a reduction in sethoxydim efficacy on at least one grass species. Dicamba, atrazine plus dicamba, atrazine plus bentazon, bromoxynil, primisulfuron, CGA-152005 plus primisulfuron, MON 12000, and flumetsulam plus clopyralid plus 2,4-D (NAF-73) were evaluated further on the efficacy and foliar absorption of sethoxydim applied to giant foxtail, large crabgrass, and shattercane. In timing studies, applying all herbicide combinations at 7 or 3 d before sethoxydim application eliminated significant antagonistic interactions. However, applying NAF-73, primisulfuron, or CGA-152005 plus primisulfuron 1 d prior resulted in a reduction in sethoxydim efficacy on at least one grass species. Dicamba, atrazine plus dicamba, and atrazine plus bentazon decreased 14C-sethoxydim absorption 9 to 63% across grass species. Replacing crop oil concentrate (COC) with DASH increased sethoxydim absorption when applied with these herbicides but not to the full extent of sethoxydim applied alone with DASH. Sethoxydim efficacy was retained or improved with DASH when applied with dicamba, atrazine plus dicamba, atrazine plus bentazon, or bromoxynil. When primisulfuron, CGA-152005 plus primisulfuron, MON 12000, or NAF-73 was applied with 14C-sethoxydim no effect on sethoxydim absorption was observed. DASH was less effective than COC at restoring sethoxydim efficacy when applied with these herbicides.

The influence of secondary soil disturbance on the emergence pattern and seed bank depletion of an annual weed community in a long-term, no-tillage corn cropping system was determined in 1992 and 1993. As a component of this research, the seed bank was characterized prior to implementation of soil disturbance treatments. The seed bank was initially composed of common lambsquarters, redroot pigweed, and giant foxtail, with approximately 55, 36, and 8% of the total viable seeds, respectively. The remaining 1% was comprised of five other species in 1992 and eight in 1993. The spatial distribution of viable seeds of each species, except common lambsquarters and redroot pigweed, was described by a negative binomial distribution. Three dispersion indices indicated that seeds of individual and total weed species were aggregated and that the level of aggregation of viable seeds of a species was associated with seed density; at lower seed densities, the level of aggregation was greater. Soil disturbance increased common lambsquarters emergence 6-fold in 1992 relative to nondisturbed soil, but did not influence emergence in 1993. Rainfall was about 50% less in 1993. In contrast, soil disturbance increased giant foxtail and redroot pigweed emergence approximately 6- and 3-fold in 1992 and 1993, respectively. Seedling emergence associated with soil disturbance, relative to nondisturbed soil, increased seed bank depletion of common lambsquarters 16-fold in 1992, and giant foxtail and redroot pigweed and average of 6- and 3-fold in 1992 and 1993, respectively. These results indicated that soil disturbance increased seedling emergence and seed bank depletion of the predominant species in the weed community of a long-term, no-tillage system, but that this response was dependent on rainfall for common lambsquarters.

Greenhouse and laboratory studies were conducted to determine the effects of tank-mixing the sodium salt of dicamba (Na-dicamba) with imazethapyr on the efficacy and foliar absorption of imazethapyr, applied with non-ionic surfactant (NIS) or methylated seed oil (MSO), by shattercane, giant foxtail, and large crabgrass. The effects of various salt formulations of dicamba and the addition of ammonium sulfate on efficacy, 14C-absorption and on foliar spray retention by the same species were also evaluated. Na-dicamba antagonized imazethapyr efficacy by reducing 14C-absorption. Using MSO instead of NIS prevented antagonism when Na-dicamba was applied at 70 and 140 g/ha and reduced the severity of the antagonism at greater application rates by greatly increasing 14C-absorption compared to NIS. Reductions in 14C-absorption and spray retention were due to the salt formulations of dicamba rather than the parent acid. The addition of ammonium sulfate prevented dicamba antagonism of imazethapyr toxicity to grassy weeds by maintaining 14C foliar absorption and spray retention at normal levels.

The recent introduction of glufosinate-resistant and glyphosate-resistant crops provides growers with new options for weed management. Information is needed to compare the effectiveness of glufosinate and glyphosate on annual weeds. Greenhouse trials were conducted to determine the response of barnyardgrass (Echinochloa crus-galli), common lambsquarters (Chenopodium album), common ragweed (Ambrosia artemisiifolia), fall panicum (Panicum dichotomiflorum), giant foxtail (Setaria faberi), large crabgrass (Digitaria sanguinalis), and velvetleaf (Abutilon theophrasti) to glufosinate and glyphosate. The response of velvetleaf and common lambsquarters was investigated at multiple stages of growth. Glufosinate and glyphosate were applied to each weed species at logarithmically incremented rates. The glufosinate and glyphosate rates that provided a 50% reduction in aboveground weed biomass, commonly referred to as GR50 values, were compared using nonlinear regression techniques. Barnyardgrass, common ragweed, fall panicum, giant foxtail, and large crabgrass responded similarly to glufosinate and glyphosate. Common lambsquarters 4 to 8 cm in height was more sensitive to glufosinate than glyphosate. In contrast, 15- to 20-cm tall-velvetleaf was more sensitive to glyphosate than glufosinate.