Velvetleaf, eastern black nightshade, wild mustard, common cocklebur, green foxtail, and yellow foxtail, grown for 4 weeks in nonaerated nutrient solution, developed satisfactorily compared to plants grown in soil. For experiments involving certain weed species grown in nutrient solution, aeration may be unnecessary.

High herbicide costs and uncertainty about annual weed control at planting have limited adoption of no-till spring wheat production systems in the northern Great Plains. Chlorsulfuron, metsulfuron, and CGA-131036 at 10 to 20 g ai ha–1 plus nonionic surfactant generally controlled both emerged kochia and wild mustard equally well (>80%) whether or not combined with glyphosate at 250 g ha–1 plus nonionic surfactant. In two of three trials persistent phytotoxic residues of these sulfonylurea herbicides in soil controlled both weeds better in midseason and early summer 1 yr after treatment than did glyphosate, which has only foliar activity. While the absolute net returns of different treatments varied among herbicides, relative net returns were insensitive to changes in either herbicide or wheat price. Herbicide use tended to boost net returns for no-till spring wheat in years with good weather but depressed net returns in a drought year. Chlorsulfuron at 10 and 20 g ha–1 increased net returns in all three trials. Metsulfuron and combinations of either metsulfuron or chlorsulfuron with glyphosate had variable effects on net returns.

Field experiments were established to determine the dose and timing of DPX-A7881 applied postemergence for control of weeds in winter rapeseed. Wild mustard and shepherdspurse were effectively controlled by DPX-A7881. Control of these weeds by DPX-A7881 was dependent upon growth stage. The later the growth stage at time of herbicide application the poorer the control. Fall applications of DPX-A7881 provided greater control of wild mustard and shepherdspurse seedlings compared to spring applications. The 0.010 kg ai ha-1 dose was as effective in controlling susceptible weed species as 0.030 kg ai ha-1. Control of common lambsquarters and redroot pigweed by DPX-A7881 was poor. Regardless of timing or amount of herbicide applied, DPX-A7881 did not significantly reduce dry weights of either barnyardgrass or green foxtail. Doses of DPX-A7881 ranging from 0.010 to 0.030 kg ai ha-1 did not injure or adversely affect winter survival of rapeseed seedlings. Rapeseed yield and seed quality were not affected by DPX-A7881 applied postemergence.

A technique based on the relationship between leaf area index (LAI) and the transmittance of direct sunlight was developed for the in situ study of competition for light between plant species. Field studies were conducted in 1984 and 1985 using monocultures and mixtures of rapeseed (Brassica napus L.), wild mustard (Sinapis arvensis L. # SINAR), and common lambsquarters (Chenopodium album L. # CHEAL). LAI estimated nondestructively by this method agreed closely with LAI determined by conventional destructive techniques. Light measurements at several heights in the canopy were used to determine the vertical distribution of canopy leaf area. Combining this information with species heights allowed the separation of the canopy LAI into individual species LAI, from which light competition could be estimated by calculating the sunlit LAI of each species. The technique permits many detailed measurements in the same canopy throughout the growing season. The light sensor required is not costly and is simple to operate and to maintain.

2,4-D diethanolamine control of kochia was influenced by the source of water used as the spray carrier. Sodium bicarbonate in one water source related to the reduced kochia control. Sodium bicarbonate in a water spray carrier antagonized 2,4-D control of all plant species evaluated. Antagonism increased with the tolerance of a species to 2,4-D, concentration of sodium bicarbonate, and spray volume. Sodium bicarbonate antagonism of 2,4-D phytotoxicity was greatest with low temperature and relative humidity.

The inheritance of resistance to dicamba in wild mustard was determined by making reciprocal crosses between a resistant (R) population derived from a field treated repeatedly with auxin-type herbicides, and a known susceptible (S) population. The resulting F1 hybrids were selfed to produce F2 populations and backcrossed to the S parent. At the three- to four-leaf stage, parental, F1, F2, and backcross populations were screened for resistance to dicamba at three dosages (50, 200, and 400 g ai ha−1). F1 progeny survived all dosages and exhibited levels of injury similar to the R parental population. F2 populations segregated in a 3:1 ratio of R to S phenotypes. Progeny of backcrosses segregated in a 1:1 (R:S) ratio. Responses of the F1, F2, and backcross populations to treatment with dicamba indicate that resistance is determined by a single, completely dominant nuclear allele.

Variation in dormancy level was tested in seeds of four species, each collected from three populations in 1994 and 1995 (experiment 1). Germination was tested in light and darkness on recently-harvested seeds and on those after-ripened in dry storage for one year. In addition, seeds from each of eight individual plants within each of eight populations were tested for germination when recently harvested and after warm stratification or cold stratification followed by a drying period (experiment 2). Seeds from the two years differed in dormancy level in Silene noctiflora, Sinapis arvensis and Spergula arvensis. Germination percentage differed significantly among populations in Sinapis arvensis and Spergula arvensis in both experiments and in Thlaspi arvense in experiment 2. Furthermore, dormancy level in seeds from different mother plants also varied in the three species tested in experiment 2. Variations at the three levels tested (year, population and mother plant) indicate that these species have a random pattern of variation in dormancy level. It is concluded that variation in seed dormancy among mother plants, populations and years must be taken into account when testing the germination characteristics of a species and also when attempting to model weed seed bank dynamics.