Glasshouse studies were undertaken to determine the effect of imposed moisture stress on the phytotoxicity of haloxyfop; the absorption, translocation, and metabolism of 14C-haloxyfop; and 14C-photoassimilate partitioning in johnsongrass and large crabgrass. Following foliar applications of haloxyfop at 30 and 25 g ai ha–1 to large crabgrass and johnsongrass, respectively, control 15 days after treatment was 92% for nonstressed plants and less than 12% for water-stressed plants. Foliar absorption of 14C-haloxyfop was reduced by moisture stress 1, 3, 5, and 24 h after treatment (HAT) in large crabgrass and 1, 3, 5, 48, and 72 HAT in johnsongrass. Regardless of stress treatment, absorption in both species reached a maximum by 24 HAT. Translocation of the radiolabel from the treated leaf to plant parts above and below the node of the treated leaf was inhibited by moisture stress in large crabgrass and johnsongrass at all harvest intervals beginning 5 and 24 HAT, respectively. Metabolism of 14C-haloxyfop was not altered by moisture stress. Fixation of 14CO2 and subsequent distribution of the 14C-photoassimilates were reduced by moisture stress. Decreases in photoassimilate translocation were similar to reductions in 14C-haloxyfop translocation. Moisture stress reduced the phytotoxicity of haloxyfop in the two grasses, and the reduced activity of haloxyfop appeared to be partially related to changes in herbicide absorption and translocation.

In greenhouse replacement series experiments, ‘Atlantic’ and ‘Russet Burbank’ potatoes and barnyardgrass were more competitive than redroot pigweed as measured by relative competitive ability. In additive design field studies, four redroot pigweed or barnyardgrass per meter of row did not reduce Atlantic tuber yield when planted between the row following hilling (6 to 7 weeks after planting). However, as few as one barnyardgrass or redroot pigweed per meter of row reduced marketable tuber yield 19 to 33% when seeded in the row at the time of potato planting. Redroot pigweed reduced tuber yield more than barnyardgrass did in 1 yr of research. The correlation coefficients were similar for both weed density and weed biomass regressed on tuber yield. Aboveground potato biomass was not consistent in predicting total tuber yield. Furthermore, variability in aboveground potato biomass was not due to increasing weed weight or density. Neither specific gravity nor tuber quality was altered by the presence of any density of either weed species.

Experiments were conducted in the greenhouse and growth chamber to evaluate competitive mechanisms of soybean and common cocklebur during seedling growth. Soybean was approximately 1.5 to 2 times taller and was more competitive aboveground than common cocklebur during the first few weeks of growth. Common cocklebur had an approximate 20 to 50% finer root system and was more competitive belowground than soybean during early growth.

Spurred anoda and velvetleaf were grown for 40 days in controlled-environment chambers in monocultures at densities of 2, 4, 8, and 12 plants per 20-cm-diam pot and in mixed culture with all combinations of 2, 4, 8, and 12 plants of each species per pot. The day/night temperature was 29/23 C, and the photosynthetic photon flux density (PPFD) was 1000 μE m–2 s–1. Shoot dry weights and leaf areas of the two species were similar when they were grown in monoculture. However, in mixed culture spurred anoda exceeded velvetleaf in leaf area/plant and shoot weight/plant in 15 out of 16 treatments. Multiple linear regression equations relating shoot biomass/plant to the density of both species in mixed culture were calculated. Comparison of competition coefficients from these equations indicated that the competitive impact of a single spurred anoda plant was equivalent to the impact of 2.5 velvetleaf plants. In mixed culture, spurred anoda always contributed a greater proportion of the total shoot weight and total leaf area per pot than would be predicted from its proportion of the total plant population. These results indicate spurred anoda is competitively superior to velvetleaf.

Field studies were conducted in 1987 and 1988 to evaluate the control and competitiveness of common lambsquarters in soybeans when present at four densities and when removed at four time intervals. Common lambsquarters were removed by hand or treated with a postemergence herbicide application of bentazon plus acifluorfen. Common lambsquarters could remain 10 weeks following soybean emergence before a 20% soybean yield reduction occurred when weeds were removed by hand. When treatment was attempted with postemergence herbicides, a 20% yield reduction occurred in 1987 if application was not made prior to 5 weeks after emergence. In 1988, all postemergence herbicide applications failed to control lambsquarters due to drought conditions. The postemergence herbicide's degree of control was reflected in the number of remaining lambsquarters plants. Common lambsquarters seed production and germination was not influenced by postemergence herbicide application. There was a strong correlation between dry weight of uncontrolled common lambsquarters plants and seed produced per plant.

Texas panicum was grown in controlled-environment chambers in 16 day/night temperature regimes ranging from 19/11 to 34/26 C. After 33 days, maximum plant height, leaf area, and dry weight occurred at 34/26 C. The greatest number of tillers and leaves occurred at 34/16 C. Partitioning of plant biomass into stems increased with increasing night temperature, while partitioning into leaves tended to decrease. Partitioning of biomass into roots decreased with increasing night temperature at day temperatures of 19 or 24 C but not at 34 C. Plant dry matter production (DMP) was highly correlated with both leaf area duration (LAD) and net assimilation rate (NAR) during the first 2 weeks of growth. During the subsequent 3 weeks, DMP was highly correlated with LAD but not with NAR. The low-temperature threshold for growth of Texas panicum was approximately 11 C. Texas panicum attained 25% of its maximum growth at an average daily temperature of 21 C, 50% at 24 C, and 75% at 26 C. Texas panicum is unlikely to become a highly competitive weed outside the southern and southwestern United States.

The effect of soil matric potential from −0.02 to <–1.5 MPa on Texas panicum growth in drainage lysimeters covered by an automatic rainfall shelter was measured in 1984, 1985, and 1986. Rate of tiller production was faster for plants established in April than June in 1984 and 1985, but not 1986. In 1985 and 1986, dry weight was greater, but total seed production was less for plants established in April than June. Irrigation when the soil matric potential was −0.02, −0.075, or −1.5 MPa did not affect rate of tiller production in 1984. Irrigation when the soil matric potential was −1.5 MPa decreased dry weight of plants but increased seed number per panicle compared to irrigation when the soil matric potential was −0.02 MPa in 1985 and 1986. Plants grown in lysimeters irrigated at soil matric potential <–1.5 MPa in 1985 and 1986 did not wilt at 8:00 a.m.; therefore, they were not watered after establishment. These nonirrigated plants averaged 0.9 and 0.4 kg dry weight and produced 92 200 and 16 100 seeds in 1985 and 1986, respectively.

We examined effects of supplementary nitrogen on young Canada thistle stands in Alberta, Canada. Urea applied at 70 or 100 kg N ha–1 increased shoot population densities, mostly through increased root growth in the top 20 cm of soil rather than through released root bud dormancy. Nitrogen fertilization, therefore, may increase the severity of a Canada thistle infestation. In 1-yr-old stands, the number of emerged and unemerged root buds/m of root was higher near the soil surface in fertilized plots than in unfertilized plots, and no underground shoots were detected at the time of sampling. In 2-yr-old stands, more unemerged root buds/m of root were found at depths below 20 cm in fertilized plots than in unfertilized plots, and twice as many underground shoots/m of root occurred between 20 and 40 cm in fertilized plots as in unfertilized plots. However, no effect of nitrogen on the number of emerged root buds was detected. Nitrogen treatment increased shoot production only for those replanted root fragments from deeper than 60 cm in 1-yr-old stands and deeper than 160 cm in 2-yr-old stands.

In replacement experiments in the greenhouse, plant relative yield (PRY) of both eastern black nightshade and tomato increased as the proportion of nightshade plants increased in the pots, indicating that nightshade is less competitive than tomato. In field studies tomato yield was reduced by two-thirds if three nightshade plants m–1 of row were allowed to grow with tomato more than 6 weeks following tomato establishment The percent marketable fruit decreased linearly from 73% with no nightshade to 49% when nightshade were present for 12 weeks. When nightshade and tomato were transplanted together, tomato yield was 9000 kg ha–1 and 49% of the fruit was marketable, while tomato yields were 30 000 kg ha–1 and 70% of the fruit was marketable when nightshade was established 9 weeks after tomato planting.

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.

Field studies were conducted to determine the effect of green foxtail density and location on the yield of potato under dryland conditions. Total and marketable tuber yields were reduced by green foxtail densities of less than 75 plants m-2. Marketable yields were affected more by increasing green foxtail density than were total yields. Increasing weed density reduced both the number and size (tuber weight) of marketable tubers but not the specific gravity or the sucrose content of the tubers at harvest. Green foxtail growing between crop rows was as competitive with potato as plants growing within the row. The effect of weed competition on total and marketable tuber yields was more pronounced in drought years than years with normal precipitation.

Greenhouse experiments were conducted to evaluate effects of sicklepod planting depths and chlorimuron, imazaquin, and metribuzin incorporation depths on sicklepod seedling emergence and growth. There was 35 and 90% sicklepod seedling emergence from 0- and 2-cm planting depths, respectively, in untreated soil 26 days after planting; emergence decreased with each additional increment below 2 cm. Chlorimuron at 63 g ai ha reduced the number of plants present 11 days after planting at 1- and 2-cm planting depths except when unincorporated. However, deeper sicklepod planting required chlorimuron incorporation to at least 6 cm for maximum reduction of plants. Imazaquin at 140 g ai ha was not as effective as chlorimuron, but a reduction in the number of plants was noted at 1- and 2-cm planting depths when imazaquin was incorporated to 4, 6, or 8 cm. Metribuzin at 420 g ai ha consistently reduced the number of plants at all incorporation depths except when unincorporated but had little effect on emergence. Chlorimuron and imazaquin reduced sicklepod dry weight most for all planting depths when incorporated 4 to 10 and 6 to 10 cm, respectively. Metribuzin reduced sicklepod biomass at all incorporation depths.

Velvetleaf was treated at the three and one-half leaf stage with one, three, or nine drops (1 μl each) of glyphosate and an amphoteric surfactant with the concentration of the droplets adjusted so that the total amount of active ingredient applied to each plant was constant. The phytotoxicity of glyphosate to velvetleaf was dependent on both the concentration of glyphosate and surfactant within the droplet A single concentrated droplet of glyphosate and surfactant was more effective in reducing the growth of velvetleaf than were more dilute droplets in greater number but with the same total quantity of herbicide. If the surfactant concentration was increased, the loss in efficacy was negated, provided the glyphosate concentration in the droplet was sufficiently high. Also, loss in efficiency was negated at increased glyphosate concentration and diluted surfactant level per droplet. The phytotoxic response of velvetleaf treated with one or three drops was greater at 45 than 90% relative humidity. This greater response at low relative humidity continued with increased surfactant concentration in each drop. However, the phytotoxic response was greater at 90 than 45% relative humidity when velvetleaf plants were treated with nine drops. When the surfactant concentration in each drop was increased, the plant's response at the two relative humidity levels did not differ.

The dissipation of flurtamone was determined in three Georgia soils in 1987 to 1989. Flurtamone dissipation in soil was initially rapid but gradually slowed throughout the sampling interval. Dissipation was not affected by rate (0.8 or 1.7 kg ai ha-1) or application method (PPI or PRE). Dissipation rates were slightly more rapid in the Greenville and Dothan soils than in the Cecil soil, with calculated initial half-lives for each respective soil being 6 to 7, 8 to 10, and 9 to 23 days. There was no effect of previous flurtamone exposure on the dissipation rate in soil at any location.

A mixed microbial culture able to transform alachlor at a concentration of 50 μg ml-1 was obtained from alachlor-treated soil after an enrichment period of 84 days. The microbial community was composed of seven strains of bacteria. No single isolate was able to utilize alachlor as a sole source of carbon. There was no alachlor left in the enriched culture after a 14-day incubation, but only 12% of the 14C-ring-labeled alachlor was converted to 14CO2 through ring cleavage during 14 days in the basal medium amended with alachlor as a sole carbon source. The presence of sucrose as an alternative carbon source decreased the mineralization potential of the enriched culture, but sucrose increased the mineralizing ability of a three-member mixed culture. Thin-layer chromatographic analysis showed that there were four unidentified metabolites of alachlor produced by the enriched culture. Sucrose decreased the amount of two of the four metabolites. The absence of a noticeable decline in radioactivity beyond the initial 12% suggested that the side chain of alachlor was utilized as carbon source by the enriched culture. Little difference in radioactivity between growth medium and cell-free supernatant of the growth medium suggested that the carbon in the ring was not incorporated into the cells of the degrading microorganisms.

The volatilization, photolysis, microbial degradation, and field persistence of imazethapyr were studied using formulated and 14C-labeled imazethapyr. Volatilization losses from soil were less than 2%. Photodecomposition losses of up to 8% occurred from soil and up to 52% from a glass slide with no soil. Significantly greater photodecomposition occurred with chain-labeled than ring-labeled 14C-imazethapyr. The amount of 14CO2 evolution from soil treated with either ring- or chain-labeled 14C-imazethapyr was not significantly different. The total 14CO2 evolved from the soils ranged from 2.4 to 3.6% of the total 14C-imazethapyr applied to the soil. However, degradation of imazethapyr from the same soils, as determined by high-pressure liquid chromatography, indicated that 62 to 82% of the applied 14C-imazethapyr had been degraded. The degradation rate increased as soil moisture was increased from −100 to −33 kPa. Imazethapyr was more persistent in soil with the higher clay and organic matter content.

Seeds of eight weed species were heated for up to 7 days at 40, 50, 60, and 70 C in dry (2% moisture) and moist (19% moisture) Bosket very fine sandy loam to determine temperature-time treatments lethal to weed seeds. Seeds in dry soil were very tolerant to 60 C or less for up to 7 days but most seeds were killed at 70 C after 7 days. In moist soil, a few (1 to 12%) seeds of common purslane, redroot pigweed, johnsongrass, and spurred anoda survived for up to 3 days at 70 C. Some (4 to 30%) seeds of velvetleaf, pitted morningglory, and the above species survived up to 7 days at 60 C. No seeds of prickly sida and common cocklebur survived more than one-half day at 60 C. Three days at 50 C were lethal to all cocklebur seeds. Many of the sublethal treatments promoted germination of prickly sida, velvetleaf, spurred anoda, and pitted morningglory, presumably because high temperature broke dormancy of some hard seeds. The enhanced effect of heat treatments upon seeds in moist soil compared to seeds in dry soil was due to the higher moisture content of seeds, or in fruit tissues of dispersal units in moist soil. Because some seeds survived several days in moist soil at 60 and 70 C, it is unlikely that soil solarization or other natural methods of raising soil temperature will eliminate weed seeds from the field. However, high soil temperatures may reduce weed seed populations by killing heat-susceptible seeds and by breaking dormancy of hard seeds followed by thermal kill of seedlings.

Bioeconomic sugarbeet weed management models for preplant, postemergence, and layby herbicides, and late-season handweeding decisions are presented. The personal computer/spreadsheet models are based on number of weed seed in soil, field survey of weed populations, growth stages of weeds and sugarbeets, expected yield loss from weeds, herbicide weed control, weed control cost, and sugarbeet price. The models incorporate two producer risk levels. Several weed scenarios were used to verify the models for reasonable recommendations.

The performance of four sequential weed management models that assumed either low or high risk was compared to the performance of two sugarbeet consultants, one who assumed low risk and the other high risk. Weed management recommendations were performed over one growing season at two locations, each with several levels of weed populations. Recommendations for preplant, postemergence, and layby herbicide treatments or late-season handweeding differed among the four weed management levels. The high-risk management level was labor intensive and the low-risk management level was herbicide intensive. Weed populations at harvest, recoverable sucrose, and net return above weed control costs were not different among the four weed management levels. Weeds can be controlled in sugarbeets by employing weed management practices based on bioeconomic modeling.

The arcsine and square root transformations were tested on 82 weed control data sets and 62 winter wheat winter survival data sets to determine effects on normality of the error terms, homogeneity of variance, and additivity of the model. Transformations appeared to correct deficiencies in these three parameters in the majority of data sets, but had adverse effects in certain other data sets. Performing the recommended transformation in conjunction with omitting treatments having identical replicate observations provided a high percentage of correction of non-normality, heterogeneity of variance, and nonadditivity. The arcsine transformation, not generally recommended for data sets having values from 0 to 20% or 80 to 100%, was as effective in correcting non-normality, heterogeneity of variance, and nonadditivity in these data sets as was the recommended square root transformation. A majority of data sets showed differences between transformed and nontransformed data in mean separations determined using LSD (0.05), although most of these differences were minor and had little effect on interpretation of results.