Kochia growing on an industrial site where chlorsulfuron was applied repeatedly over several seasons was confirmed to be resistant to chlorsulfuron and several other acetolactate synthase (ALS) -inhibiting herbicides. In growth room experiments, resistant (R) plants were 2 to >180 times more resistant to five sulfonylurea herbicides and one imidazolinone herbicide (imazethapyr) than susceptible (S) plants, as measured by the ratio of dosages required to inhibit shoot dry matter accumulation by 50% (GR50 R/S). Similarly, in vitro assays of ALS activity indicated that from 3 to 30 times more herbicide was required to inhibit the enzyme from R plants than from S plants. Results of ALS enzyme assays indicated that R kochia was approximately equally resistant to metsulfuron, triasulfuron, and thifensulfuron, and 2.5 times more resistant to tribenuron than thifensulfuron. However, the response of R kochia growing in a spring wheat crop in the field was not consistent with results of the ALS enzyme assays. In field experiments, thifensulfuron at 32 g ai ha−1 had little effect on R kochia. In contrast, metsulfuron, triasulfuron, and tribenuron at 8 g ha−1 did not reduce R kochia seedling densities, but caused severe stunting such that 2 mo after treatment the shoot biomass of plants in untreated plots was four times greater than in sprayed plots. Herbicides with alternative modes of action including fluroxypyr, bromoxynil/MCPA ester, dichlorprop/2,4-D ester, and 2,4-D ester provided good control of R kochia in the field. Quinclorac did not reduce kochia densities, but surviving plants were stunted. To delay or avoid development of ALS inhibitor-resistant kochia populations, these alternative herbicides applied alone or in tank mixtures could be incorporated into a herbicide rotation.

Field studies were conducted from 1986 through 1989 to determine the feasibility of using clomazone in a winter wheat-corn-fallow rotation. Clomazone at 1.1 kg ai/ha did not control emerged downy brome in autumn nor did it control redroot pigweed and tumble pigweed that emerged after a spring application of paraquat at 0.6 kg ai/ha. However, clomazone plus atrazine at 0.6 plus 2.2 kg ai/ha provided weed control in winter wheat stubble from October to corn harvest 12 mo later. Corn yields from this treatment were equal to or greater than the conventional practice of applying atrazine plus glyphosate at 2.2 plus 0.4 kg ae/ha in the fall followed by a spring application of metolachlor plus dicamba at 2.8 ai plus 0.3 kg ae/ha. When kochia densities were high, clomazone plus atrazine controlled triazine-resistant kochia better than metolachlor plus dicamba. Atrazine at 2.2 kg/ha applied in autumn followed by clomazone at 0.8 kg/ha in April generally caused more corn injury than when the same rate of clomazone was applied in autumn with the atrazine. The percent of bleached corn plants varied with planter, year, time of application, and rate of clomazone applied. The optimum time to apply clomazone at 0.6 kg/ha was in autumn with atrazine. This treatment caused some corn bleaching but produced the highest corn yield over 3 yr. In a dry autumn and spring, less clomazone injury occurred with a planter equipped with row cleaners than those without. The injury pattern associated with planters was inconsistent when precipitation was average and no injury occurred in a wet autumn and spring.

Field experiments were conducted to determine the effect of CGA184927 rate, weed growth stage, and tank mixes with various broadleaf herbicides on the control of green foxtail and wild oat in spring wheat. CGA 184927 controlled green foxtail and wild oat equally well when applied at the 2- to 3- or 4- to 5-leaf stages. Green foxtail and wild oat were controlled at similar rates of CGA 184927 but the application rate giving > 90% control ranged from 22 to 90 g/ha over locations and years, indicating that CGA 184927 efficacy is sensitive to environmental conditions. CGA 184927 in tank mixtures was compatible with bromoxynil, clopyralid, and 2,4-D ester. However, tank mixing with metsulfuron or dicamba reduced activity on green foxtail and wild oat. Broadleaf herbicide activity on kochia and redroot pigweed was not reduced when such herbicides were tank-mixed with CGA 184927. Spring wheat tolerated 120 g/ha of CGA 184927. CGA 184927 provides growers with another herbicide option to control green foxtail and wild oat in wheat.

Dormant and nondormant kochia [Kochia scoparia (L.) Schrad. ♯3 KCHSC] seed populations were buried at six soil depths in Colorado. Portions of both populations remained viable for 36 months. Persistence increased with burial depth in both populations. Seed loss from the initially dormant population was limited to germination in situ, but seed loss from the initially nondormant population included significant viability loss at burial depths of 10 cm or less. Persistence of both populations was regulated by dormancy retention. Shallow tillage practices are predicted to decrease seed persistence in soil and increase successful seedling emergence. Deep tillage practices are predicted to reduce seedling emergence but increase soil seed populations.

Greenhouse-grown kochia [Kochia scoparia (L.) Schrad. # KCHSC] seedlings from populations having either a 13-yr triazine history or no triazine history were sprayed postemergence with 0, 2, or 20 kg/ha atrazine [6-chloro-N-ethyl-N′-[1-methylethyl)-1,3,5-triazine-2,4-diamine]. Fresh weight was reduced 20% in triazine history kochia treated with 20 kg/ha atrazine. Seedlings with no triazine history were killed by 2 kg/ha atrazine. Biotypes resistant to atrazine were also resistant to five other triazine herbicides. Biotypes susceptible to atrazine were susceptible to the other triazines. Atrazine-resistant biotypes were more susceptible to 2,4-D [(2,4-dichlorophenoxy)acetic acid] than atrazine-susceptible biotypes, but atrazine history had no effect on response to diuron [N′-(3,4-dichlorophenyl)-N,N-dimethylurea].

Herbicidal control of triazine-resistant (TR) kochia was evaluated in no-till grain sorghum. Herbicides were applied early preplant (EPP) or POST. In EPP experiments, herbicides plus nonionic surfactant at 0.25% v/v were applied 7, 2, or 0 wk before planting (WBP). Fluorochloridone at 0.8 kg ai/ha applied 7 or 2 WBP, pyridate at 1.0 kg ai/ha applied 2 WBP, and paraquat at 0.4 kg ai/ha applied 0 WBP controlled 94 to 99% of TR kochia; a prepackaged mixture of glyphosate plus 2,4-D at 0.3 plus 0.6 kg ae/ha and paraquat at 0.4 kg/ha applied 7 or 2 WBP controlled 71 to 82% of TR kochia; and 2,4-D ester at 0.6 kg ae/ha applied 2 WBP controlled 75% of TR kochia. Linuron at 0.8 kg ai/ha and atrazine at 2.2 kg ai/ha were ineffective. In the POST herbicide experiments, where paraquat plus metolachlor at 0.6 plus 1.7 kg ai/ha were applied 17 d before planting, various combinations and rates of bentazon plus atrazine, bromoxynil, and dicamba with adjuvants provided good control of TR kochia that was less than 8 cm tall.

Fresnel lenses are used to concentrate solar radiation to a line or point. A linear Fresnel lens (0.91 by 1.52 m, 0.74-m focal length, 0.01- by 1.52-m line focus) was investigated as a method for weed control. Field experiments were conducted to assess the effect of Fresnel lens concentrated solar radiation at various exposure times, stages of plant growth, and soil surface moisture conditions. On a dry soil surface exposure times of 1 to 10 s at 290 C resulted in control of redroot pigweed from 100% for a 1-s exposure at the cotyledon stage to 89% for a 10-s exposure at the 10-leaf stage. Redroot pigweed and kochia control was similar at exposures of 3 to 10 s, but less for kochia at 1 and 2 s. Green foxtail control was less than that of kochia and redroot pigweed. Control was reduced on a moist compared to a dry soil surface. Concentrated solar radiation holds the greatest potential for control of small dicot weeds on a dry soil surface.

Field experiments were conducted for 3 yr to determine the effect of various biological and physical factors on the operation of the weed-sensing Detectspray system. Plant detection is achieved by sensors measuring differential reflectance of red and near-infrared wavelengths of light from green plants, crop residues, and soil. Weed detection was greatly reduced 70 to 80 min after sunrise and before sunset when operated at lat 50°N because of reduced solar irradiance. Tall, dense-standing crop stubble limited detection of small weeds at the soil surface. Weed detection varied with plant species. Canola with three to four leaves consistently was detected, but wheat or green foxtail usually required five to six leaves to be detected. Small weeds were detected if present at densities greater than 70 plants m−2. Growers and commercial applicators need to be aware of the limitations of the Detectspray system to use it effectively to control weeds with concurrent reductions in herbicide use.

Two field experiments were conducted between 1990 and 1992 under sprinkler irrigation at the Research and Extension Center, Torrington, WY to determine the influence of mixed densities and durations of kochia and green foxtail interference in sugarbeet. Sugarbeet root yield and top weight generally decreased as densities of green foxtail and kochia increased whether alone or in combination. Reductions in sugarbeet root yield and above ground biomass from mixed densities of kochia and green foxtail were additive at the low and intermediate density but less than additive at the high density of either species. Sugarbeet root yield decreased as the duration of interference after sugarbeet emergence from a mixed density of kochia and green foxtail increased. Since sugarbeet plants were irrigated to avoid water stress and adequate nutrients were applied, it appears that kochia and green foxtail interfered with sugarbeet primarily for light, based on light and height measurements. Season-long as well as duration of interference did not show any significant effect on sucrose content. Based on regression analysis the lowest densities of kochia and green foxtail required to reduce root yield were approximately 0.3 and 0.06 plants/m of row, respectively. The minimum duration of time that 0.5 kochia and 3.0 green foxtail plants/m of row can interfere with sugarbeets before root yield is economically reduced was approximately 3.5 wk after sugarbeet emergence.

Emergence of sugarbeets (Beta vulgaris L. ‘MonoHy D2’) from soil was reduced by germinating kochia [Kochia scoparia (L.) Schrad. ♯ KCHSC] seed at densities greater than 1 seed/cm2 when the fungus Rhizopus sp. was present. Water-soluble exudates from germinated kochia seed did not influence Rhizopus growth in vitro or sugarbeet germination. Cell-free culture extracts of Rhizopus reduced sugarbeet germination and radicle elongation. There appeared to be an interaction between kochia and Rhizopus, but the responsible compounds were not identified.

Studies were conducted to determine the usefulness of HOE-39866 (HOE-00661) in chemical fallow systems on the Canadian prairies. HOE-39866 at 0.5 to 1.0 kg ai/ha controlled Russian thistle, kochia, green foxtail, wild oats, and wheat comparable to paraquat, glyphosate, and glyphosate plus the isopropylamine salt of 2,4-D. However, control of barley with HOE-39866 was unacceptable. HOE-39866 was compatible in tank mixtures with ammonium sulfate, paraquat, chlorsulfuron, and metsulfuron. Ammonium sulfate improved weed control when HOE-39866 was applied at 0.25 kg/ha but not at 0.75 kg/ha. Adding paraquat at 0.07 to 0.21 kg ai/ha to HOE-39866 improved control of grass species over HOE-39866 alone. Adding chlorsulfuron and metsulfuron to HOE-39866 provided greater initial control of certain species as well as residual control of many weeds. HOE-39866 alone or in conjunction with other herbicides is an alternative to the herbicides used in chemical fallow systems.

The methyl ester of thiameturon {3-[[[[(4-methoxy-6-methyl-1,3,5-triazin-2-yl)amino] carbonyl] amino] sulfonyl]-2-thiophencarboxylic acid} toxicity to kochia [Kochia scoparia (L.) Schrad. # KCHSC] increased with surfactant concentration in the spray to 0.25% (v/v). High soil nitrogen fertility (165 ppm) enhanced kochia susceptibility to thiameturon compared to low nitrogen fertility (65 ppm). Nitrogen plus surfactant in the spray only partially overcame the effect of low soil nitrogen but did enhance thiameturon toxicity to kochia at all fertilities. Petroleum oil plus surfactant enhanced thiameturon so that kochia fresh weight reduction was similar regardless of soil fertility. Thiameturon toxicity to kochia generally increased with an increase in temperature regardless of relative humidity (RH) or adjuvants. An RH of 90 to 95% enhanced thiameturon toxicity to kochia regardless of temperature or adjuvants, except for petroleum oil plus surfactant with the low (10:8 C day:night) temperature regime. A simulated rain of 2 mm within 24 h after treatment reduced thiameturon toxicity to kochia. Drought stress (≤25% of field capacity) after thiameturon application reduced toxicity regardless of spray additives. The results of the various experiments indicated that thiameturon phytotoxicity would be greatest to kochia growing with high temperature and high RH, adequate soil moisture and nitrogen fertility, and when applied with petroleum oil plus surfactant.

Imidazolinone-resistant and -tolerant corn hybrids give growers a new weed control option. Field experiments were conducted in 1993 and 1994 to evaluate imazethapyr for controlling weeds in no-till corn planted into winter wheat stubble in a winter wheat–ecofallow corn rotation. Imidazolinone-tolerant (IT) and imidazolinone-resistant (IR) corn were protected genetically from injury by imazethapyr that was applied preplant, preemergence, or postemergence to ‘Pioneer Brand 3417,’ ‘Pioneer Brand 3417 IR,’ ‘ICI Seeds 8532,’ and ‘ICI Seeds 8532 IT’ hybrids. No difference in corn injury occurred between IR and IT corn. Imazethapyr applied to resistant or tolerant corn hybrids could be used to control weeds in ecofallow corn. Imazethapyr at 35 or 70 g ai/ha controlled triazine-resistant kochia better than the standard herbicide treatment of metolachlor plus cyanazine.

Scanning electron micrographs of spray droplet residual on wheat, sunflower, and kochia indicated that salts and various adjuvants applied with glyphosate affected deposit crystal content, thickness, and contact with the leaf surface. Spray deposits of glyphosate applied with diammonium sulfate contained distinct crystals, which related to enhanced toxicity of glyphosate applied alone, or to overcoming antagonism of glyphosate toxicity by calcium chloride, when applied to wheat. In general, glyphosate applied with antagonistic calcium chloride salt formed spray deposits that were amorphous, thick, and without crystals. Glyphosate sprayed with nonantagonistic diammonium sulfate and ammonium chloride salts had deposits with crystals and an evenly spread residue beneath the crystals. The various micrographs indicate that the antagonism of glyphosate phytotoxicity by salts may be in part from physical entrapment of glyphosate in the spray deposit. Glyphosate spray droplet residue contact with wheat, sunflower, and kochia surfaces related to observed differences in glyphosate toxicity to these species.

Kansas and North Dakota kochia populations identified as chlorsulfuron resistant (R) contained 20 and 30% susceptible (S) plants, respectively. Biotypes that were chlorsulfuron R or S were selected from each field R or S collection and selfed through three generations in the greenhouse. Chlorsulfuron at 7.6 and 17.8 g ai/ha suppressed shoot biomass of the Kansas and North Dakota R biotypes by 50%, respectively, which was a 30- and 105-fold greater dose than that required to reduce the respective S biotypes growth 50%. The R and S kochia biotypes are diploid with 2N = 18 chromosomes. Chlorsulfuron resistance is inherited in kochia as a dominant trait controlled by a single nuclear gene. Thus, the resistance trait can be spread by seed and pollen.

Field experiments were conducted over 3 yr at two locations in northwest Kansas to evaluate the efficacy and crop tolerance of EXP 31130A alone and with other herbicides in corn. EXP 31130A alone and in combination with acetochlor, atrazine, or metolachlor controlled kochia and redroot pigweed 93% or greater regardless of location, year, or tillage system. Green foxtail control in 1997 and 1998 was > 90% with EXP 31130A in combination with chloroacetamide herbicides but varied among experiments with EXP 31130A alone. Control of puncturevine with EXP 31130A alone or in tank mixtures was 75% or greater at five of six sites. EXP 31130A alone and in combinations caused minor, early-season, corn leaf bleaching and/or stunting under conventional tillage. However, no injury was detected in no-till systems. In 1996, no-till corn receiving EXP 31130A treatments yielded similarly or up to 29% more than hand-weeded corn. Yields did not differ among treated, untreated, and hand-weeded corn in 1996 under conventional tillage, where weed interference was not as intense as under no-till conditions. Conventional-tillage corn receiving EXP 31130A alone or in tank mixtures in 1997 yielded similarly to hand-weeded corn. Averaged over experiments, corn yield in 1998 increased by 10 to 18% with applications of EXP 31130A alone or in combinations compared to untreated corn.

Calcium chloride in the spray carrier antagonized the toxicity of diethanolamine 2,4-D and sodium 2,4-D, dimethylamine MCPA, sodium bentazon, dimethylamine dicamba and sodium dicamba, sodium acifluorfen, imazamethabenz, ammonium imazethapyr, and isopropylamine glyphosate to kochia in greenhouse experiments. Diammonium sulfate overcame calcium chloride antagonism of the above herbicides, except for glyphosate and imazethapyr. Diammonium sulfate or ammonium nitrate adjuvants overcame calcium chloride and sodium bicarbonate antagonism of dicamba toxicity to kochia and enhanced toxicity of sodium dicamba to nearly equal that of dimethylamine dicamba.

Field observations indicate that sulfonylurea-resistant kochia may germinate at lower soil temperatures and/or germinate more rapidly than susceptible kochia in the absence of herbicide. To investigate this possibility, seeds from three resistant and two susceptible kochia accessions were germinated at temperatures ranging from 4.6 to 13.2 C on thermal gradient plates. At 4.6 and 13.2 C, germination rates of all resistant accessions were higher than susceptible accessions, while germination rates of one resistant accession were higher than susceptible accessions at 7.2 and 10.5 C. Percent germination of all resistant accessions was significantly higher than susceptible accessions after 48 h at 4.6 C. At higher temperatures, percent germination of some resistant accessions was higher after 12 or 24 h, but germination of all accessions was similar at later times. HPLC analysis revealed that seeds from resistant accessions contained about 2-fold higher free levels of branched chain amino acids than seeds from susceptible accessions. The results indicate that mutations conferring resistance to sulfonylurea herbicides in these kochia accessions may concomitantly reduce or abolish acetolactate synthase sensitivity to normal feedback inhibition patterns, resulting in elevated levels of branched chain amino acids available for cell division and growth during early germination.

Field experiments were conducted in 1983 and 1984 at two locations to determine the influence of various densities and durations of kochia interference in sunflower. Sunflower achene yield and dry weight were reduced by all densities of kochia, averaged over locations and years. Season-long competition by kochia densities of 0.3, 1, 3, and 6 plants/m of row decreased sunflower achene yield 7, 10, 20, and 27%, respectively. Sunflower achene yield and sunflower dry weight decreased as weeks of kochia competition increased. Only 2 weeks of kochia competition after sunflower emergence decreased sunflower achene yield 6%. Sunflower achene yield loss increased as the duration of kochia competition increased. Sunflower 200 achene weight, oil content, and plant height were not influenced by various densities or durations of kochia competition.

Field studies were conducted to determine the influence of annual herbicide treatments plus cultivation on weed populations and corn yields in ridge-till corn during a 3-yr period at Mitchell, NE, and a 7-yr period at North Platte, NE. When the experiment was initiated at North Platte, no weeds were present before corn planting. It took 4 yr before triazine-resistant kochia became a problem before corn planting in plots treated with atrazine, but these were controlled by other operations prior to corn harvest. In the cultivated check, green foxtail densities before harvest increased from 0 in 1985 to 32 plants 100 m−2 in 1991. Annual applications of dicamba plus 2,4-D 10 d early preplant followed by cultivation controlled triazine-resistant kochia and velvetleaf, but common lambsquarters, nightshade species, and green foxtail increased. Volunteer corn was controlled with cultivation. After 3 yr at Mitchell, the annual weed population increased 10-fold in the cultivated check. Thus, corn yields were reduced 64% with two cultivations compared with an annual early preplant application of dicamba plus 2,4-D followed by alachlor plus cyanazine PRE and two cultivations. With two cultivations under low annual weed populations at North Platte, grain yield from the cultivated check treatment was not different from annual treatments of herbicides after 7 yr. Metolachlor plus atrazine occasionally caused a reduction in corn grain yields.