Effects of the herbicides SC-0224 and glyphosate on the pool levels of free amino acids, soluble protein, and protein synthesis in inflated duckweed were compared. SC-0224 caused larger increases than glyphosate in the pool levels of amino acids; the increases caused by SC-0224 were similar, however, to those caused by trimethylsulfonium iodide (TMS-I). Expressed on a per gram fresh weight basis, none of the treatments changed soluble protein or the incorporation of 14C-leucine into soluble protein. On a per flask basis (allowing for decreased growth in treated flasks), both herbicides and TMS-I decreased soluble protein and 14C-leucine incorporation. Decreases in soluble protein and 14C-leucine incorporation were equal for SC-0224 and TMS-I but larger than for glyphosate. These data indicate that differences in the phytotoxicity of SC-0224 and glyphosate may be due to the action of the trimethylsulfonium portion of the SC-0224 structure.

The effect of ammonium sulfate (AMS) on efficacy and on absorption and translocation of sethoxydim in wild oats and barley was investigated under controlled environmental conditions. Increases in efficacy in the presence of AMS were relatively small. The rate of sethoxydim required to reduce dry weight 50% was reduced from 0.08 kg a.i. ha−1, for both species, to 0.07 and 0.06 kg ha−1 for wild oats and barley, respectively, in the presence of added AMS. In short-term experiments, uptake of 14C from 14C-labeled sethoxydim 0.5 and 1 h after application was increased approximately twofold with the addition of AMS. AMS had little effect on sethoxydim absorption beyond 1 h after application. Translocation at 1 h after application was unaffected by AMS. However, translocation 12 and 24 h after application was increased with AMS. It is postulated that the translocation increase results indirectly from the increase in absorption. The observed increase in absorption with the addition of AMS is evident only when crop oil concentrate (COC) is also present In model systems, the addition of AMS enhanced sorption of sethoxydim into Isolated cuticles but had no effect on movement into excised roots.

Greenhouse and laboratory studies were conducted to determine the basis of differential response of two corn hybrids to the chloroacetanilide herbicide metolachlor. In greenhouse experiments, metolachlor at 6.7 kg ha−1 reduced the height of the susceptible ‘Northrup-King 9283’ corn by 53% relative to untreated controls and caused extensive visible injury 14 d after treatment Under the same conditions, the height of metolachlor-treated ‘Cargill 7567’ corn seedlings was reduced by only 18% without any visible herbicide injury. The 14C-metolachlor was more rapidly absorbed by the emerging shoot of the metolachlor-susceptible hybrid, Northrup-King 9283. Thus, differential metolachlor tolerance may be due in part to processes at the level of herbicide uptake. Metabolism experiments revealed that both hybrids were able to conjugate 14C-metolachlor with glutathione at similar rates. However, glutathione S-transferase activity increased earlier during seedling development and reached higher activities in the metolachlor-tolerant hybrid, Cargill 7567.

The basis for increased phytotoxicity of foliar-applied atrazine at high temperature in common bean and redroot pigweed was investigated. Plants were grown under low (15/10 C), medium (25/20 C), or high (35/30 C) temperature regimes. Atrazine absorption by plants grown under different temperatures increased with increasing temperatures in both species. Greater than 90% of absorbed atrazine remained in treated leaves and translocation was not altered by temperature in both species. Metabolism of atrazine by both hydroxylation and glutathione-conjugation was greater in plants grown at 35/30 than 15/10 C in both species. Foliar-applied atrazine reduced extractable photosystem II (PS II) activity as temperature increased in both species. Studies were also conducted on thylakoid membranes from plants not treated with atrazine. The I50 for atrazine inhibition of PS II decreased and affinity of atrazine binding to thylakoid membranes increased as temperature increased in both species. We concluded that the increased phytotoxicity of atrazine at high temperatures is caused by enhanced foliar absorption and greater affinity of atrazine for the binding site.

Photoacoustic spectroscopy was used to study effects of atrazine and diuron on excised leaves of triazine-susceptible (S) and -resistant (R) biotypes of black nightshade. Changes of oxygen and photothermal components were compared to photochemical fluorescence quenching obtained by fluorimetry. After 1 h incubation in an aqueous solution of atrazine (0 to 200 μM), oxygen component of the photoacoustic signal was strongly decreased in the S biotype while the R biotype was not affected. Also, reoxidation of the primary quinone acceptor (QA−) of photosystem (PS) II of the S biotype was lower than that of the R biotype. With diuron treatments, changes in the characteristics of these biophysical signals were the same in both R and S biotypes. Both oxygen component and photochemical fluorescence quenching were decreased in treated leaves of the R and S biotypes. By using modulated oxygen and heat emissions, and the ratio of the initial inflection point (I) to the fluorescence maximum (P) as herbicide bioassay indicators, we showed that the photoacoustic spectroscopy was also a reliable technique for whole plant studies. Inhibition of photosynthesis was maximal 2 d after onset of treatment with atrazine (200 μM). Inhibitors of PSII did not induce a significant increase of heat emission in leaves which otherwise showed phytotoxic symptoms after treatment By using the photoacoustic technique, it was possible to obtain useful information on photosynthetic activity under herbicide stress, suggesting that pulsed oxygen emitted by leaves could be used to quantify susceptibility or to detect resistance to many types of photosynthetic inhibitors in weeds and crop plants.

Greenhouse and laboratory studies were conducted to determine the extent of cross-resistance of chlorsulfuron-resistant sugarbeet (CR1-B) to other herbicides that inhibit acetolactate synthase (ALS) and to determine the physiological basis of resistance. Cross-resistance to metsulfuron, imazaquin, and imazethapyr was not evident, while only marginal cross-resistance was observed to triasulfuron, DPX-L5300, and nicosulfuron. CR1-B was moderately resistant to chlorsulfuron and chlorimuron and was highly cross-resistant to thifensulfuron and primisulfuron. Further greenhouse studies demonstrated that CR1-B was not significantly injured by thifensulfuron and primisulfuron applied at or exceeding the field use rate. Studies with 14C-primisulfuron showed that differential absorption or metabolism of primisulfuron could not account for the observed resistance. ALS enzyme assays showed that the CR1-B ALS enzyme activity was 66, 26, and 13 times less sensitive to chlorsulfuron, thifensulfuron, and primisulfuron inhibition, respectively, compared to ALS enzyme extracted from sensitive sugarbeets. An altered ALS enzyme, which is less sensitive to sulfonylurea herbicide inhibition, appears to be the physiological basis of resistance.

Sethoxydim reacts spontaneously with water resulting in immediate structural changes. Simulation of field conditions of light, moisture, oxygen, pH, and soil and evaporation on siliceous surfaces duplicated this lability. Sethoxydim degradation was enhanced by alkaline conditions, ultraviolet and incandescent light, and adsorption on solid surfaces. No sethoxydim was detected immediately after application to moist soil. Less than 2% extractable sethoxydim was present in dry soil after 24 h.

Foliar absorption of picloram by broom snakeweed, a rangeland shrub, was investigated. Picloram uptake into leaf, axillary bud, and stem tissues was similar. In addition, picloram uptake by leaf tissue from greenhouse- and field-grown broom snakeweed did not differ. Picloram accumulated rapidly and absorption saturated between 15 min and 1 h of application; no further absorption occurred through 72 h with maximum uptake ca. 15% of applied picloram. Picloram content increased linearly with increasing external picloram concentration, implying that movement of the herbicide across the cuticle is via diffusion. Absorption was dependent on relative humidity and temperature with the greatest uptake at 94% relative humidity and 35 C, respectively. Absorption was pH dependent; picloram absorption was greatest at pH 4 and least at pH 8. In addition, picloram absorption was less at pH 3 compared to pH 4. These results provide evidence that picloram is absorbed across the cuticle via simple diffusion and absorption is dependent on environmental conditions and solution pH at and following application.

Research was conducted in soybean and common cocklebur to determine if the synergistic interactions of clomazone plus metribuzin and clomazone plus linuron were due to the effect of one herbicide on root uptake, partitioning, or metabolism of the other. Treatments consisted of 14C-clomazone alone and combined with metribuzin or linuron, 14C-metribuzin alone and combined with clomazone, and 14C-linuron alone and combined with clomazone. Root uptake and partitioning of clomazone applied alone in soybean differed compared to clomazone plus metribuzin. Root uptake and partitioning of metribuzin or linuron did not differ when applied alone or combined with clomazone. Binding of clomazone or its metabolites in an unextractable form may be a method of deactivating clomazone by soybean, but not by common cocklebur. Levels of parent clomazone were higher in common cocklebur roots when clomazone was combined with metribuzin and linuron compared to clomazone done. Levels of parent metribuzin were higher in soybean roots, and in common cocklebur roots and shoots when clomazone was combined with metribuzin compared to metribuzin alone. Levels of parent linuron were greater in soybean shoots when linuron was applied with clomazone compared to linuron alone. These results indicate that the metabolism of metribuzin and linuron is altered in both species when clomazone is applied, leading to increased phytotoxicity.

Fourteen tomato genotypes, eastern black nightshade, and 35 Lycopersicon accessions were screened for tolerance to acifluorfen. Tolerant and susceptible genotypes occurred in most species. Fifteen genotypes were chosen for further study depending on their fresh weight after acifluorfen treatment Over all 15 genotypes, there was no correlation between trichome density and acifluorfen tolerance; however, in L. esculentum, cultivars with the most trichomes were the most tolerant There was an inverse relationship between stomata density and tolerance. Amount and composition of epicuticular wax and cuticle thickness did not correlate to acifluorfen tolerance.

Acifluorfen tolerance in eastern black nightshade somaclones was characterized in two experiments. One experiment determined the involvement of absorption, translocation, and metabolism in acifluorfen tolerance. Less than 6% of the applied 14C-acifluorfen was absorbed. There were no differences in acifluorfen absorption between susceptible and tolerant somaclones. More 14C-acifluorfen was translocated in the susceptible than the tolerant somaclones. The susceptible somaclone did not metabolize acifluorfen while some somaclones (i.e., EBN-3A) metabolized 14C-acifluorfen. A second experiment determined the tolerance of the somaclones to oxyfluorfen, diquat, and paraquat Most acifluorfen-tolerant somaclones were tolerant to oxyfluorfen but were susceptible to diquat and paraquat One somaclone, EBN-3A, was extremely tolerant to acifluorfen, paraquat, and diquat.

Studies were conducted to determine the mechanism of acifluorfen tolerance within the Lycopersicon genus. Absorption of 14C-acifluorfen was not correlated with tolerance. There was a negative correlation (r = −0.57) between absorption 24 h after treatment and wax density. No other surface characteristic correlated with absorption. Less than 3% of absorbed 14C was translocated and there was no metabolism of acifluorfen. All genotypes were susceptible to paraquat, and acifluorfen-tolerant genotypes had lower levels of ascorbate than susceptible genotypes, implying that free radical protectant systems were not involved in tolerance. Genotypes varied in amounts of chlorophyll a, chlorophyll b, and total chlorophyll but the differences did not correlate to acifluorfen tolerance.

The influence of nitrogen form on bentazon uptake and toxicity to soybean cell cultures and medium pH was examined. Soybean cell growth was completely inhibited at 40 μM bentazon when cells were cultured in a Murashige and Skoog medium containing 20 mM ammonium and 38 mM nitrate. However, bentazon, up to 100 μM, did not affect the growth of cells cultured in B5 medium (Gamborg B5 medium containing 2 mM ammonium and 25 mM nitrate). Twenty-minute 14C-bentazon uptake experiments on 48- and 96-h-old cells demonstrated that 14C uptake was nitrogen-type dependent, with cells cultured in AMM medium (B5 medium containing 38 mM nitrate and 12 mM ammonium) accumulating 5 to 10 times more 14C than those in B5 or NIT media (B5 containing 50 mM nitrate). Differential bentazon uptake between ammonium and nitrate-containing media appears to be attributable to the effect of nitrogen form on pH. From an initial pH of 5.5, the pH of AMM medium decreased to 4 by 48 h. The pH of NIT or B5 medium increased to approximately 7 from 5.5. Changes in pH are likely attributable to cellular maintenance of ionic balance; NH4+ and NO3− uptake results in H+ and OH- efflux, respectively. Methylamine at 12 mM did not result in a decrease in medium pH. Bentazon, a weak acid (pKa 3.3), would be expected to penetrate the plasma-membrane faster in the molecular form at low pH. Support for a nitrogen pH theory is provided by the finding that 14C-bentazon uptake was similar for ammonium and nitrate-containing media when media were buffered.

Laboratory studies were conducted to determine the effect of various factors on germination of dogfennel and yankeeweed. Dogfennel seed were found to be strongly photoblastic with no germination in the dark. Yankeeweed seed were moderately photoblastic, with 12% germination occurring in the absence of light Germination for both species increased in response to red light (650 nm), indicating phytochrome regulation. At the soil surface, dogfennel and yankeeweed emergence was 40 and 48%, respectively, but declined rapidly with increasing soil depths where dogfennel germination was lower than that of yankeeweed. Yankeeweed germination was 60 to 75% from 10 to 30 C while dogfennel germination was 45 to 70% between 15 to 30 C. Both species germinated over a broad range of pH (6 to 10) with the highest germination occurring at pH 8. Yankeeweed and dogfennel were moderately tolerant to water stress, but yankeeweed tolerated higher water stress than dogfennel. Both species germinated over a wide range of conditions, possibly enhancing adaptation to many diverse environments.

The effect of different levels of tillage and weed management on population, distribution, and germination of weed seed was evaluated in three tillage systems at Arlington and Hancock, WI, in 1989 and 1990. Over 60% of all weed seed in the top 19 cm of soil were found in the top 1 cm in no-tillage at both sites. As depth increased, concentration of weed seed declined logarithmically in no-tillage. In chisel plowing, over 30% of seed were in the top 1 cm and seed concentration decreased linearly with depth. Moldboard plowing had uniform distribution of weed seed in the top 19 cm of soil. Preemergence metolachlor plus atrazine decreased weed seed population by 50% compared with no treatment over all tillage systems. One year of the herbicide treatment plus handweeding to assure weed-free conditions did not reduce seed numbers in chisel plowing or moldboard plowing compared to herbicide alone. Seed numbers with no-tillage and weed-free conditions decreased by 40% relative to herbicide alone. Common lambsquarters germination was 40% greater in moldboard plowing and chisel plowing compared with no-tillage. Germination was highest in seed taken from 9 to 19 cm deep in moldboard plowing and from 0 to 9 cm deep in chisel plowing.

Shattercane seed survival during soil burial was highly dependent on attached glumes. Shattercane seed tightly enclosed by glumes averaged 5 and 53% germination after 4 mo of winter burial in 1988 and 1989, respectively. Shattercane caryopses (seed without glumes) survival averaged 0.5 and 17% compared to 17 and 41% when treated with seed fungicides in 1988 and 1989, respectively. Shattercane caryopses tannin and lignin contents were higher than for cultivated sorghum caryopses. Glume tannin was four times higher and glume lignin was five times higher than in the caryopsis. Shattercane seed survival was positively correlated with glume tightness, caryopsis lignin, and glume tannin. Tannin and lignin appear to function as barriers to microbial invasion resulting in higher shattercane seed resistance to overwinter demise. Attempts to isolate fungal inhibitors from shattercane seed were unsuccessful.

Field studies were conducted in southern Ontario to determine the critical period of weed control in grain corn and the influence of weed interference on corn leaf area. The Gompertz and logistic equations were fitted to data representing increasing durations of weed control and weed interference, respectively. The beginning of the critical period varied from the 3- to 14-leaf stages of corn development However, the end of the critical period was less variable and ended on average at the 14-leaf stage. Weed interference reduced corn leaf area by reducing the expanded leaf area of each individual leaf and accelerating senescence of lower leaves. In addition, weed interference up to the 14-leaf stage of corn development impeded leaf expansion and emergence in 1989.

Round-leaved mallow interference in spring wheat and flax was investigated under field conditions in southern Manitoba. Additionally, the growth of mallow alone and in a wheat crop was compared. In six of seven trials, wheat yield losses due to mallow interference were not significant. In a seventh trial, where mallow densities of up to 237 plants m−2 were recorded, wheat yields were reduced up to 15%. In contrast, significant flax yield losses occurred in each of three trials where maximum mallow densities ranged from 21 to 52 plants m−2. From the regression equations it was calculated that 20 mallow plants m−2 caused flax yield losses of 33, 9, and 10% in 1987, 1988, and 1989, respectively. Periodic sampling of mallow plants growing alone and in wheat, and regression analysis of these data using a logistic function as a biological model of plant growth indicated that mallow growth was severely suppressed by wheat By the eighth week after emergence, the lamina area and shoot dry matter of mallow plants growing in wheat was less than 3% of plants growing alone. Similarly, in wheat, mallow produced less than 1% of the seed produced by plants growing alone. This extreme suppression of mallow growth corresponded with an 80 to 90% decrease in photosynthetically active radiation penetrating the wheat canopy for approximately six continuous weeks, beginning 4 wk after crop emergence.

Field experiments were established in 1989 and 1990 at the Southern Piedmont Conservation Research Center near Watkinsville, GA, to determine effects of coastal bermudagrass density on cotton in a conservation tillage system. Cotton height, canopy width, leaf area indices, and seed cotton yields were determined at coastal bermudagrass densities of 0 to 3600 kg ha−1 as achieved by herbicide inputs. Soil water measurements were recorded in cotton plots with a range of coastal bermudagrass densities using time domain reflectometry. Cotton growth and yields were reduced by coastal bermudagrass competition both years of the study. At the highest coastal bermudagrass density of 3600 kg ha−1, cotton height was reduced compared to cotton alone as early as 5 wk after planting. Seed cotton yields were reduced 25% at the highest coastal bermudagrass densities both years of the study. At the 15-cm soil depth, coastal bermudagrass significantly reduced soil water in cotton. Soil water in cotton at 30, 45, and 60 cm was not affected by coastal bermudagrass.

The relationships between the actual amount of spring-applied trifluralin detected in soil at seeding, initial injury to flax, and crop growth and yield were investigated in southern Manitoba over three growing seasons. As the amount of trifluralin in the soil increased, flax density and dry matter production decreased, such that at a soil concentration equivalent to 1 kg ai ha−1 trifluralin, the two were reduced by 40 and 49%, respectively. Recovery from early-season injury was characterized by enhanced crop growth rates (CGRs) and net assimilation rates (NARs) of surviving plants during the remainder of the growing season. Maximum recovery occurred in plots where trifluralin levels in the soil were between 0.8 and 1 kg ha−1 at seeding. During the interval between stem elongation and bud initiation, CGRs and NARs of flax in the trifluralin-treated plots exceeded those of flax in the untreated plots by up to 1.5 and 1.2 times, respectively. Additionally, the number of branches per plant increased linearly as trifluralin amounts in the soil increased. Flax seed yield was decreased by trifluralin as described by the equation: flax seed (% of untreated control) = 104.9 - 13.3[trifluralin detected (kg ha−1) at seeding]. Based on this equation, trifluralin levels in the soil of up to 0.7 kg ai ha−1 caused less than a 5% reduction in flax yield under weed-free conditions.