Laboratory studies were conducted to determine the effect of SAN 582 on the absorption, translocation, and metabolism of sethoxydim in johnsongrass and soybean. 14C-sethoxydim absorption in johnsongrass and soybean was enhanced 4 h after application when tank mixed with SAN 582. Absorption in johnsongrass increased from 18% with 14C-sethoxydim applied alone to 65% when applied with SAN 582. Absorption in soybean increased from 30% with 14C-sethoxydim applied alone to 83% when applied with SAN 582. The addition of crop oil concentrate also enhanced foliar absorption of 14C-sethoxydim. Eight hours after application, foliar absorption in johnsongrass increased from 22% with 14C-sethoxydim applied alone to 61% when 14C-sethoxydim was applied with crop oil concentrate. Foliar absorption in soybean increased from 38% with 14C-sethoxydim applied alone to 59% when 14C-sethoxydim was applied with crop oil concentrate. When 14C-sethoxydim was applied in combination with crop oil concentrate and SAN 582, foliar absorption was 84% or more in both johnsongrass and soybean 4 h after application and did not increase over time. Minor differences in translocation were observed, but these differences were not sufficient to account for the increase in foliar activity observed when SAN 582 is tank mixed with sethoxydim. SAN 582 did not affect metabolism of sethoxydim in either species. Based on these data, it appears that SAN 582 increases the efficacy of sethoxydim by enhancing foliar absorption.

In vitro acetolactate synthase (ALS) activity from three commercial imidazolinone-resistant corn hybrids (ICI 8692 IT, Pioneer 3751 IR, and Ciba 4393 IMR) was compared to imidazolinone-sensitive isogenic hybrid controls for sensitivity to 11 herbicides representing four classes of ALS-inhibiting herbicide chemistry. Acetolactate synthase activity from Pioneer IR and Ciba IMR was cross-resistant to all four classes of ALS inhibitors, ranging from 48- to 5,000-fold. The ICI IT hybrid displayed only four- to eightfold resistance to the six imidazolinone herbicides and the pyrimidinylthiobenzoate herbicide, pyrithiobac, but no cross-resistance to the sulfonylurea and triazolopyrimidine sulfonanilide herbicides. The four- to eightfold enzyme resistance to imidazolinone herbicides provides whole-plant resistance; however, the sevenfold enzyme resistance to pyrithiobac was insufficient to afford whole-plant protection to a field application rate of the herbicide. A second imidazolinone-specific resistance allele, XI-12, currently under commercial development, was examined for the level of dominance at the enzyme level. In the heterozygous state, imazethapyr resistance was fivefold, compared to 250-fold in the homozygous condition, indicating XI-12 is a semidominant trait. No cross-resistance to nicosulfuron or primisulfuron was observed in the heterozygous XI-12 hybrid extracts nor to nicosulfuron in the XI-12 homozygote; however, a fivefold resistance to primisulfuron was detected in the XI-12 homozygote.

Three sugarbeet selections differing in cross-resistance to three classes of acetolactate synthase (ALS)-inhibiting herbicides have been developed using somatic cell selection. Sugarbeet selections resistant to imidazolinone herbicides, Sir-13 and 93R30B, do not metabolize [14C]-imazethapyr any faster or differently than sensitive, wild-type sugarbeets or a sulfonylurea-resistant/imidazolinone-sensitive selection, Sur. ALS specific activity from the three herbicide-resistant selections ranged from 73 to 93% of the wild-type enzyme extracts in the absence of herbicide, indicating enzyme overexpression was not a factor in resistance. Acetolactate synthase from Sir-13 plants showed a 40-fold resistance to imazethapyr but no resistance to chlorsulfuron or flumetsulam. Polymerase chain reaction amplification and sequencing of two regions of the ALS gene spanning all known sites for ALS-based herbicide resistance in plants indicated a single nucleotide change in the Sir-13 gene (G337 to A337) resulting in a deduced substitution of threonine for alanine at position 113 in the sugarbeet amino acid sequence. Sur ALS was not significantly resistant to imazethapyr, but was 1,000- and 50-fold resistant to chlorsulfuron and flumetsulam, respectively. Sur gene sequencing indicated a single nucleotide change (C562 to T562) resulting in a serine for proline substitution at position 188 of the ALS primary structure. The 93R30B nucleotide sequence indicated two mutations resulting in two deduced amino acid substitutions: threonine for alanine at position 113 plus serine for proline at position 188. The 93R30B double mutant incorporated the changes observed in each of the single mutants above and correlated with higher resistance levels to imazethapyr (> 1,000-fold), chlorsulfuron (4,300-fold), and flumetsulam (200-fold) at the ALS level than observed in either of the single mutants. 93R30B represents the first double mutant derived by a two-step selection process that incorporates two class-specific ALS-inhibitor resistance mutations to form a single broad cross-resistance trait. The interaction of the two altered amino acids is synergistic with respect to enzyme resistance vs. the resistance afforded by each of the individual mutations.

Acetolactate synthase (ALS)-inhibiting herbicide carryover in soil can severely affect sugarbeets grown in the year(s) following application. Two newly developed imidazolinone-resistant (IMI-R) sugarbeet somatic cell selections (Sir-13 and 93R30B) were examined for magnitude of resistance and extent of cross-resistance to other classes of ALS inhibitors and compared to a previously developed sulfonylurea-resistant (SU-R) selection, Sur. In vitro shoot culture tests indicated Sir-13 resistance was specific to imidazolinone (IMI) herbicides at approximately a 100-fold resistance compared to the sensitive control sugarbeet. Sur was 10,000-fold resistant to the sulfonylurea (SU) herbicide, chlorsulfuron, and 40-fold resistant to the triazolopyrimidine sulfonanilide (TP) herbicide, flumetsulam, but not cross-resistant to the IMI herbicides. 93R30B was selected for IMI-R from a plant homozygous for the SU-R allele, Sur, and displayed similar in vitro SU-R and TP-R as Sur, but also displayed a very high resistance to various IMI herbicides (400- to 3,600-fold). Compared to the sensitive control, Sir-13 was 300- and > 250-fold more resistant to imazethapyr and imazamox residues in soil, respectively. Response by whole plants to postemergence herbicide applications was similar to that observed in shoot cultures. Sir-13 exhibited > 100-fold resistance to imazethapyr as well as imazamox, and 93R30B showed > 250-fold resistance to both herbicides. 93R30B showed great enough resistance to imazamox to merit consideration of imazamox for use as a herbicide in these sugarbeets. Sir-13 showed a two- to threefold higher level of resistance in the homozygous vs. heterozygous state, indicating that like most ALS-inhibitor resistance traits, it was semidominantly inherited.

Weed species composition and density were recorded in three identical field experiments established 26 to 30 yr ago in southern Sweden. Each experiment compared three 6-yr crop rotations and four rates of nitrogen application. The rotations differed by having (1) a 2-yr rotational grassland, (2) a 2-yr mixed rotational grassland (legume/grass), or (3) spring wheat followed by fallow. Other crops in the rotations were winter turnip rape, winter wheat, spring oats, and spring barley. Using multivariate analyses, the relative importance of site, crop, crop rotation, and nitrogen application rate on the weed flora was determined. The greatest difference was found between sites, and the second most important factor was crop species. Nitrogen application rate weakly influenced the weed flora, while differences between crop rotations were hardly detectable.

For wild oats, persistence characters such as seed production and seed dormancy may be affected by genetic variation and several environmental factors during the development of the parental plant. However, the effect of varying photoperiods on such characters is unclear. Previous studies have concentrated on natural populations and have not studied the genetic variability within the population. Consequently, a study was conducted to examine how photoperiod (10, 12, 14, 16, and 18 h at 20 C) influenced the persistence of different members of a synthetic population of wild oats. This synthetic population consisted of several isogenic lines with differing degrees of seed dormancy that originated from one region in North America. All lines were photoperiod sensitive, quantitative long day plants, with an increase in time to maturity for all lines (about 78 to 213 d) when photoperiod was reduced from 18 to 10 h. The lines within this synthetic population (with the exception of one, M73) showed a similar degree of photoperiod sensitivity. This may be expected, as the lines are from one region with the same photoperiod environment. It could be concluded that such a photoperiod sensitivity is a beneficial character that has allowed persistence of these lines in this region. When photoperiod was reduced from 18 to 10 h, plants produced fewer seeds (about 141 to 61 primary seeds per plant) with a higher degree of seed dormancy (about 88 to 54% germination in 10−4 M gibberellic acid; GA3). The reduced seed production under the shortest photoperiod (10 h) was due to poor panicle exsertion, which resulted in poor development of basal florets. There was no consistent relationship between photoperiod and other plant characters such as tiller production, caryopsis weight, and water content. However, significant relationships were found between seed dormancy characters and other plant characters such as maturity time, caryopsis weight, and water content under certain photoperiod treatments.

This research was conducted to evaluate the light requirement for redroot and smooth pigweed germination in soil, and how this requirement is affected by germination temperature and seasonal periodicity in seed dormancy. Seed enclosed in nylon mesh bags was buried in the field in December 1993 and 1994 and was recovered throughout the spring and summer of the following year, respectively. Germination was highest with red light or at 30 C. The requirement for red light was more pronounced at 20 vs. 30 C. The saturating fluence of red light was as low as 3 μmol m−2 in buried seed and 1,000 μmol m−2 in unburied control seed, depending on germination temperature. The effect of light and germination temperature pigweed germination also changed throughout the growing season. Our results indicate that light may be a requirement for germination in only the most dormant weed seed in the soil seedbank.

This research was conducted to determine the environmental conditions necessary for development and expression of very low fluence (VLFR) germination sensitivity, and to determine the roles of type I phytochrome, gibberellic acid (GA) biosynthesis, and nitrate in this process. Redroot pigweed seed was subjected to pregermination incubation regimes of 5, 12, and 23 C for up to 21 d in a −1.2 MPa polyethylene glycol solution in the dark. Development of VLFR sensitivity was most pronounced at 23 C, and induction of germination by the lowest fluence tested (3 μmol m–2) was greater at a germination temperature of 30 than 20 C. In dormant smooth pigweed seed, development of VLFR sensitivity occurred only when seed was subjected to a prechilling treatment to overcome primary dormancy. The instability of the fluence response of seed subjected to pregermination conditions favorable for development of VLFR was consistent with type I phytochrome accumulation and degradation after photoconversion. In redroot pigweed seed, inhibition of GA biosynthesis during pregermination incubation resulted in the partial attenuation of VLFR sensitivity. The addition of 75 ppm nitrate to pregermination and germination media enhanced VLFR sensitivity. Our results suggest that development of VLFR sensitivity is due to cooperative action between type I phytochrome and phytochrome-independent GA biosynthesis. In the soil seedbank, this sensitivity may be augmented in elevated soil nitrate environments.

The effect of reduced water availability on glyphosate efficacy and adventitious shoot growth in male and female clones of Canada thistle was studied. Water availability was regulated with polyethylene glycol (PEG) in hydroponically grown plants or by withholding water from soil-grown plants. In hydroponic media, there was 50% more adventitious shoot growth from male plants than from female plants. Both PEG and foliarly applied glyphosate reduced the number of adventitious shoots, regardless of gender. In soil, the same number of adventitious shoots formed on untreated male and female plants. However, when glyphosate was applied to plants growing under dry conditions, there was 75% more adventitious shoot growth from males than females. Distribution of glyphosate was similar in male and female plants. Approximately 23% of applied 14C-glyphosate was transported throughout Canada thistle plants within 10 d of treatment regardless of gender or moisture condition. Gender differences in capacity for vegetative reproduction may alter the sex ratio of Canada thistle populations in the field following glyphosate application.

Peak germination and emergence of common lambsquarters usually occur in early to mid-spring, but both processes can occur during summer and fall. Seeds produced by different common lambsquarters cohorts (seedlings that emerge at nearly the same time) may vary in dormancy status, response to environmental conditions, and response to management factors. Therefore, experiments were conducted to determine the influence of different cohorts on common lambsquarters demography. Field experiments determined plant density, biomass, and seed production of different common lambsquarters cohorts within a crop-free community of annual weed species that included redroot pigweed, giant foxtail, and velvetleaf. Common lambsquarters plant density and aboveground biomass were greater for a mid-May cohort than for early June, late June, mid-July, or early August cohorts, but seed production of the mid-May and early June cohorts did not differ (about 192,000 seeds m−2) and was greater than that of other cohorts (111,500 seeds m−2 or less). In the laboratory, percent germination prior to stratification (exposure of seeds to low temperatures) was less for seeds harvested from early May and late May cohorts (≥ 9%) than those of mid-June or early July cohorts (≤ 75%). After stratification in the field, percent emergence (seedlings per number of planted seeds) and mean emergence time were similar among early May, late May, mid-June, and early July cohort seed sources, and were not influenced by shallow burial in soil. These results suggest that recruitment from seeds produced by different common lambsquarters cohorts is similar, but proportional to the number of seeds produced by each cohort.

Experiments were conducted to examine morphological variation among hemp dogbane populations. Rootstocks collected from 16 sites throughout Michigan and Illinois were used to establish nurseries in East Lansing, MI, and Champaign, IL. Growth, stem characteristics, and leaf characteristics were measured for each ecotype at both nurseries. Differences among ecotypes were observed for all measurements except emergence date and growing degree days to emergence. The number of shoots per plot produced by the ecotypes ranged from 5 to 54 and shoot height ranged from 69 to 126 cm. Ecotypes spread laterally at different rates, with the most aggressive covering 19 times more ground area than the least aggressive. Total shoot dry weight accumulation varied greatly among ecotypes. Some ecotypes could be identified from others by their unique leaf shape. Shoot number, shoot height, and ground area covered were greater for plants grown in Michigan than in Illinois. Differences in growth and morphological characteristics among ecotypes were not correlated with the geographical region where they were collected. Differences in measurements between the two nurseries illustrate the role of environment and genetics in the growth and morphology of this plant species.

Understanding patterns of weed seedling emergence within a growing season and over years is important to develop models to predict optimum timing of weed management practices. A study was conducted in a field with no previous velvetleaf infestations to describe emergence patterns following seed burial at three depths in two tillage systems. Freshly harvested velvetleaf seeds were planted 0, 2, and 6 cm deep in moldboard plowed (MP) and no-tillage (NT) corn stubble in October 1990. Velvetleaf seedling emergence was monitored over the following 4 yr in continuous corn. Emergence was higher in NT than in MP plots throughout 4 yr of observation. The first growing season following seeding, emerged seedlings represented 9.3 to 15.8% of the seeds sown in NT, compared with 0.1 to 0.8% of seeds sown in MP. After four growing seasons, emerged seedlings were 12.5 to 25% of seeds sown in NT but only 6 to 7.4 % of seeds sown in MP. Emergence was consistently higher from the 0-cm depth than from the 6-cm depth in NT, but seeding depth did not influence emergence in MP due to mixing of the soil during tillage. Velvetleaf emergence was related to growing degree days (base 7.5 C), with greater consistency in NT than in MP. Averaged over years and planting depths, 50% velvetleaf emergence occurred within 8 and 13 d of the predicted date in NT and MP systems, respectively.

A screening method was used to characterize seed thermal responses of prostrate knotweed and common purslane, two important weeds invading wheat in the humid Pampa. Through this method, it was possible to detect thermal conditions that induce or break dormancy in both species. In addition, we were able to quantify changes in dormancy level in seed populations as a function of time of burial after dispersal, through changes in width of the thermal range within which germination can occur. Plotting the overlap of this thermal range and observed soil temperature throughout the year allowed the prediction of the seedling emergence period. This prediction was in agreement with observed seedling emergence in the field for both species, during 2 consecutive yr. From the analysis carried out under laboratory conditions, it was also possible to estimate required thermal time for germination of the nondormant fraction of the population and the base temperature above which thermal time is accumulated. The results obtained from this study are the basis for the formulation of seed germination models that predict not only the occurrence of seedling emergence in the field, but also the dynamics of germination within those periods.

Field studies were conducted in Colorado and New Mexico to examine growth and development of spurred anoda accessions from Colorado, Mississippi, New Mexico, and North Carolina. Accessions were grown in a common garden in both locations. Leaf and stem weight ratios, leaf area ratio, and leaf area per plant were determined. North Carolina and Mississippi accessions were similar in morphology and appearance. Leaf shape, degree of pubescence, and coloration were different in the Colorado and New Mexico accessions. At both sites, the Colorado accession was taller and the canopy wider than other accessions. In Colorado in 1993, North Carolina and New Mexico accessions had the highest total weight followed by Colorado, then Mississippi. In 1994, final total weights of North Carolina, Mississippi, and New Mexico accessions were similar and greater than the Colorado accession. All accessions had similar final total weights in New Mexico in 1993. In 1994, Mississippi, North Carolina, and New Mexico accessions had similar total weights. The Colorado accession flowered earlier than other accessions. Seeds from Mississippi and North Carolina accessions grown in Colorado were heavier than the New Mexico or Colorado accession. This research demonstrates why making inferences of weed biology for variable species that occur over diverse geographic and climatic conditions is difficult and why regionally specific data are needed for variable species.

Field studies were conducted to determine the effect of common cocklebur interference in early-maturing (maturity group IV) soybean planted in April, May, and July. Common cocklebur density and length of interference did not affect soybean height, canopy width, or node number at any planting date. Removal of common cocklebur 4 weeks after emergence (WAE) prevented reduction of soybean leaf area, stem dry weight, dry leaf weight, dry pod weight, and seed yield. Aboveground biomass for common cocklebur emerging in July was less than biomass of April or May plantings. Common cocklebur planted into soybean 2, 4, or 8 wk after soybean emergence did not reduce soybean yield. Under parameters of this study, planting date was not a significant factor in yield reduction. Interference from one common cocklebur plant per 1.8, 0.9, and 0.3 m of soybean row for 8 wk reduced yields 7, 14, and 30%, and full-season interference reduced yields 16, 33, and 65%, respectively. The Arkansas Weed Management Computer program closely predicted actual yield loss for early-maturing soybean.

Field studies were conducted at three locations in 1993 and 1994 to evaluate weed control and crop response to metolachlor plus combinations of 0.5 × and 1 × label rates of imazaquin applied preplant and imazethapyr applied early postemergence or postemergence in no-till narrow-row soybean production. Giant foxtail, common ragweed, common cocklebur, and large crabgrass population reductions were greater with sequential preplant metolachlor plus imazaquin followed by early postemergence or postemergence imazethapyr than with preplant metolachlor plus imazaquin or early postemergence/postemergence imazethapyr alone. Ivyleaf morningglory was not effectively controlled by any herbicide program. Pennsylvania smartweed populations were reduced with all herbicide treatments. Soybean yields with treatments utilizing 0.5 × rates were usually equal to 1 × rates if imazethapyr was applied early postemergence or postemergence. Net income with reduced herbicide rates was equal to full-label rates and provided no greater risk to net income.

Greenhouse studies were conducted to determine purple and yellow nutsedge response to selective placement of a 5-cm layer of pyrithiobac sodium-treated soil above, below, or above and below nutsedge tubers. Pyrithiobac sodium at 36 or 72 g ae ha−1 applied postemergence as foliar, soil, or foliar and soil treatments also was evaluated. Pyrithiobac sodium applied above, below, or above and below nutsedge tubers reduced yellow and purple nutsedge shoot number, shoot regrowth, and root-tuber dry weight at least 90%. Foliar-only treatment of pyrithiobac sodium was less effective at reducing emerged purple and yellow nutsedge numbers than application to soil only or to foliage and soil. Best reduction in yellow and purple nutsedge growth with pyrithiobac sodium was obtained with soil-incorporated treatments.

Herbicides have been used to control tall larkspur to prevent cattle deaths. There is some evidence that tall larkspur may become more toxic and more palatable during the desiccation process following herbicide treatment. A series of studies were conducted to measure toxic alkaloid concentration in tall larkspur following treatment with metsulfuron, picloram, and glyphosate. Herbicides were applied to larkspur plants grown in a greenhouse (1990), to field plots infested with larkspur (1993), and to individual larkspur plants in the field (1995). Leaves were harvested up to 14 or 28 d following treatment, and toxic alkaloids were measured. Metsulfuron increased toxic alkaloid concentration in the 1990 greenhouse study and in 1993 field plot studies, and increased both concentration and absolute amount of toxic alkaloids in 1995 individual plant treatments. Alkaloids in plants treated with picloram either remained unchanged or declined slightly in all three studies and were similar to control plants. In the 1995 study, glyphosate caused the relative concentration of alkaloids to increase as the plants desiccated, but the absolute amount of alkaloids was similar to control plants. Picloram and glyphosate did not reduce alkaloid concentration; thus, the risk of poisoning remains until plants desiccate. Metsulfuron increased alkaloid concentration, thus increasing the risk of poisoning. Cattle should not be allowed to graze sprayed areas until larkspur desiccates and withers.

Field studies were conducted from 1993 through 1995 to determine potential reductions in herbicide use and associated cost savings by utilizing a weed-sensing sprayer, named Detectspray, to control weeds throughout the fallow season and to control perennial weeds after crop harvest. The Detectspray system gave comparable weed control to conventional broadcast spraying on 80% of the application dates and reduced glyphosate/dicamba use over the fallow season by 19 to 60%. This reduced herbicide use resulted in cost savings of $6 to $32 ha−1. A fallow treatment that combined two herbicide applications with the Detectsprayer plus one to two wide-blade tillage operations was less costly than conventional tillage at two of 11 sites and at all sites retained more surface crop residues to reduce the risk of erosion. Postharvest glyphosate use on quackgrass with the Detectsprayer was reduced 50 to 78% compared to broadcast applications and resulted in cost savings of $16 to $25 ha−1. Clopyralid use on Canada thistle with the Detectsprayer was reduced 71 to 80%, with cost savings of $44 to $50 ha−1. The Detectspray system is a useful tool to effectively manage weeds in conservation fallow and reduced tillage cropping systems.