Phytotoxicity of five substituted urea herbicides 3-(3,4-dichlorophenyl)-1,1-dimethylurea (diuron), 3-(p-chlorophenyl)-1,1-dimethylurea (monuron), 3-phenyl-1,1-dimethylurea (fenuron), 3-hexahydro-4,7-methanoindan-5-yl) −1,1-dimethylurea (norea), and 3-(m-trifluoromethylphenyl)-1,1-dimethylurea (fluometuron) at 0, 10, 100, and 1000 ppm were determined in factorial combination at four urea nitrogen levels of 0, 45, 450, and 900 ppm with three Aspergilli: A. niger, A. sydowi, and A. tamarii. Response interactions were apparent, with all three fungi most tolerant for fenuron and least for diuron. Apparent tolerance order of the three intermediates were: A. niger, norea > fluometuron > monuron; A. sydowi, fluometuron > monuron > norea; and A. tamarii, fluometuron > norea > monuron. Oat (Avena sativa L.) bioassay for residual herbicide toxicity indicated significant differences in herbicide degradation rates between these three fungi at 5, 10, and 20 ppm in Eufaula sand. Diuron was more rapidly degraded than monuron at these levels with fluometuron and norea somewhat intermediate. A. niger was most effective in degradation of these herbicides with A. tamarii greater than A. sydowi. High nitrogen levels in soil organic matter amendment generally favored increased rates of urea herbicide degradation.

Citron melon is a monoecious, hairy annual vine commonly found in citrus orchards, and cotton and peanut fields. Information is not available on the effect of various environmental factors on the germination of citron melon. Laboratory and greenhouse experiments were carried out in 2011 and 2012 to determine the effect of light, temperature, salinity, pH, simulated water stress, and depth of sowing on the germination of citron melon. Citron melon germination was affected by various environmental factors. Highest germination was observed at day/night temperatures of 25/20 to 30/25 C regardless of light conditions. At temperatures below 25 C and beyond 35 C, germination declined and was higher under dark condition than light. Germination decreased as osmotic potential became more negative (−0.3 MPa to −1.5 MPa) and salt concentration increased (50 to 350 mM). No germination was observed at > −0.9 MPa and ≥ 300 mM salt concentrations. However, germination was observed over a broad range of pH (3 to 9) and up to 10-cm sowing depths. Seeds sown at the surface did not germinate but maximum germination (88 to 96%) occurred at 2- to 4-cm depth. The results of this study suggest that citron melon can grow in a wide range of climatic conditions and therefore can persist in Florida because of favorable weather and environmental conditions.

Five species of Nymphaeaceae, representing four genera, were collected from various sites in New Jersey and their tissues analyzed for 12 elements. Three species were separated into leaf blades and petioles before the mineral analyses were made. Variations in the concentrations of many elements were noted between these two structures. Except for the petioles of these three species, the N content of the plants appeared to be sufficiently high so that no extra N would be required to prepare composts from them.

Clomazone dissipation in soil was examined in field and laboratory experiments. Field studies suggested a potential for injury to rotational crops such as wheat. Field half-lives were 5 to 29 d (average of 9 field studies was 19 d) for the Etowah clay loam (fine-loamy, siliceous, thermic typic Paleudult) and Lily loam (fine-loamy, siliceous, thermic typic Hapludult) soils. Clomazone had an average half-life of 34 d under lab conditions, indicating slower dissipation in the lab than in the field. Clomazone was moderately adsorbed to soil as indicated by a Kd of about 1, and a Kom of 52 in the two soils.

Fall-planted longspine sandbur began to emerge in April, peaked in late April or May, and continued at low levels through October. During the first year after seeding, 98% of the total seedlings emerged prior to June. Fall-planted puncturevine began to emerge in late April or May and continued through October. Puncturevine emergence was multipeaked and 75% of each season's total emerged prior to mid-July. A similar number of puncturevine seedlings emerged the second and third years after planting as in the first. The emergence pattern for a species was similar each year regardless of how long the seed had lain in the soil. Longspine sandbur required 7 to 13 weeks from emergence to heading and produced approximately 2600, 1300, 180, and 3 spikes per plant when planted in May, June, July, and August, respectively. Puncturevine flowered within 3 to 4 weeks after emergence when temperatures were favorable and produced an average of 5600, 5200, 3600, and 200 burs per plant when planted in May, June, July, and August, respectively.

Four field experiments conducted over 3 yr indicated that cultivation alone failed to prevent johnsongrass [Sorghum halepense (L.) Pers.] from reaching densities that severely reduced yields of cotton (Gossypium hirsutum L. ‘Acala SJ-2’). Density of johnsongrass in plots cultivated four times and hoed weekly for 8 weeks after emergence was reduced to 1 shoot/m2 at harvest compared to 74 shoots/m2 for plots that were only cultivated. In addition to a 60% average yield loss of seed cotton, yield losses ranging from 40 to 76%, ginning losses were also greater from cultivated than from hand-weeded plots. Compared to cultivated plots, supplementing cultivation with two postemergence applications of 3.0 kg/ha of DSMA (disodium methanearsonate) increased the average yield of cotton by 20% and reduced perennial johnsongrass densities by 64% at harvest. Although yields were improved by applying DSMA, they averaged 40% less than those of hand-weeded plots. The temporary weed control obtained with DSMA was profitable in terms of the additional lint and seed obtained, but insufficient cotton was produced to pay expenses for producing the crop by any of the methods of weed control. High labor costs for hoeing prevented this treatment from being profitable.

Experiments were conducted to examine the use of spectral reflectance curves for discriminating between plant species across moisture levels. Weed species and soybean were grown at three moisture levels, and spectral reflectance data and leaf water potential were collected every other day after the imposition of moisture stress at 8 wk after planting. Moisture stress did not reduce the ability to discriminate between species. As moisture stress increased, it became easier to distinguish between species, regardless of analysis technique. Signature amplitudes of the top five bands, discrete wavelet transforms, and multiple indices were promising analysis techniques. Discriminant models created from data set of 1 yr and validated on additional data sets provided, on average, approximately 80% accurate classification among weeds and crop. This suggests that these models are relatively robust and could potentially be used across environmental conditions in field scenarios.

In field studies, ‘Regal’ sweet potato greatly reduced yellow nutsedge growth when the two species were grown together using standard cultural practices. At the end of the growing season, yellow nutsedge shoot dry weight per m2 in plots where the two species were planted together was less than 10% of shoot weight in plots where nutsedge was grown alone. Presence of yellow nutsedge did not markedly affect sweet potato growth. When grown together in a greenhouse experiment designed to minimize the competitive effects of sweet potato on yellow nutsedge, yellow nutsedge growth was reduced more than 50% by sweet potato 8 and 12 weeks after planting. The most polar fraction of serially extracted sweet potato periderm tissue was highly inhibitory to yellow nutsedge root growth. These results indicate that sweet potato interference with yellow nutsedge under field conditions is partially due to allelopathy.

Nonradioactive and 14C-labeled arsenical herbicides were applied to foliage of purple nutsedge (Cyperus rotundus L.) and yellow nutsedge (Cyperus esculentus L.) grown under greenhouse and growth chamber conditions. Disodium methanearsonate (DSMA) controlled purple nutsedge better at 20 and 29 C than at 13 C. Monosodium methanearsonate (MSMA) was as effective in controlling this weed at 13 C as at 20 and 29 C. DSMA and MSMA provided 80% or greater control of yellow nutsedge grown at the three temperatures. When plants were treated with 14C-DSMA and 14C-MSMA, greater radioactivity was detected in yellow nutsedge than in purple nutsedge. The apparent differential herbicide penetration of purple and yellow nutsedge leaves is believed to have contributed substantially to the control of nutsedge observed in this study.

Dormancy is a critical factor for the survival and persistence of weedy species. Contemporary approaches can be used to identify genes that regulate dormancy directly or indirectly to elucidate key mechanisms, signals, and pathways. Several domesticated plant species have been used as model systems to mark quantitative trait loci (QTL) that affect dormancy in seeds and vegetative propagules directly. A few weedy species have also been used to mark QTL and to determine dormancy genes using microarray analysis. Given the number of serious weeds worldwide and the role that dormancy plays in their persistence, developing fundamental knowledge on dormancy is an important step toward developing new strategies for weed management. This paper describes current research and outlines some weeds that might be candidates for dormancy investigations using molecular genetic and genomics approaches. An underlying theme in the selection of weeds for dormancy investigations is their relation to crop species and the ability to adapt existing resources to investigate dormancy in weedy plants.

The fungal protein Nep1, produced by Fusarium oxysporum f. sp. erythroxyli in liquid culture, caused extensive necrosis to Centaurea maculosa when water solutions of Nep1 (5 µg ml−1) and an organosilicone surfactant (1,1,1,3,5,5,5-heptamethyltrisiloxanyl propyl-methoxy-poly[ethylene oxide]) were applied as foliar sprays. Nep1 did not cause necrosis when applied with a nonionic surfactant or organosilicone surfactant plus unrefined corn oil. Plant age, protein concentration, organosilicone surfactant concentration, and the presence of a dew period influenced the amount of necrosis caused by Nep1. The addition of an 18-h dew period after treatment resulted in an increase of 10% or more in foliar necrosis at the 0.313 and 1.25 µg ml−1 (0.40 and 1.62 g ai ha−1) Nep1 concentrations. Increasing the spray volume from 129 ml m−2 (1,291.3 L ha−1) to 516 ml m−2 (5,165.2 L ha−1) more than doubled the amount of foliar necrosis caused by the 0.313 µg ml−1 (0.40 g ai ha−1 vs. 1.62 g ai ha−1) Nep1 concentration. A maximum necrosis rating of 95% was reached by 1.25 µg ml−1 Nep1 applied at 516 ml m−2 (6.46 g ai ha−1) followed by an 18-h dew period. Nep1 (6.46 g ai ha−1) remained active when coapplied to Centaurea maculosa with the herbicides 2,4-D or glyphosate (0.13 to 2.58 kg ai ha−1), causing foliar necrosis prior to the herbicides killing Centaurea maculosa. An increase in the organosilicone surfactant concentration from 1 to 2 ml ai L−1 was required to achieve levels of Nep1-induced necrosis on Centaurea maculosa acclimated to direct sun comparable to levels achieved on greenhouse-grown plants. Repeated application of Nep1 (6.48 g ai ha−1) 3 wk after an initial treatment (6.48 g ai ha−1) prevented the recovery of acclimated Centaurea maculosa. Greater damage was caused to acclimated Centaurea maculosa when Nep1 was applied near the middle of the day (80% necrosis at 10:00 A.M. and 85% necrosis at 2:00 P.M.) compared to early or late in the day (25% necrosis at 6:00 A.M. and 10% necrosis at 6:00 P.M.).

Quinclorac drift has been speculated as the cause of injury to tomato crops throughout northeast Arkansas. In this study, we set out to determine whether tomato plant injury and yield reduction were correlated with simulated quinclorac drift. Experiments were carried out at Fayetteville, AR, in 1999 and 2000. Maximum plant injury (visual ratings) was about 20% when plants were treated with one, two, or three quinclorac applications (weekly intervals beginning at first flower) at 0.42 g ai ha−1 (0.001 times the normal use rate to simulate drift). Maximum plant injury ranged from 48 to 68% with quinclorac simulated drift treatment of 42 g ha−1. Overall, increasing quinclorac rate and number of applications increased tomato injury. In both years, tomato plant fresh-weight accumulation was not influenced by one, two, or three applications of quinclorac at 0.42 g ha−1 compared with the untreated control. In 1999, increasing the rate of quinclorac from 0.42 to 4.2 g ha−1 reduced plant fresh-weight accumulation. In 2000, there was no significant difference in plant fresh weight when plants were treated with quinclorac at 2.1 to 4.2 g ha−1. Evaluation of the herbicide rate effect indicated that quinclorac at 0.42 g ha−1 did not reduce tomato fruit yield (total weight of edible fruit) compared with the untreated control, but yield decreased as rate increased above 0.42 g ha−1. Increasing the number of applications generally decreased tomato yield, and overall as maximum visual plant injury increased, tomato yield reduction ALSo increased linearly. We conclude that quinclorac at simulated drift rates can adversely affect tomato plant growth and yield.

The control of three summer annual grass weeds with herbicides during establishment of forage grasses was studied near Concord and Mead, NE, in 1984, 1985, and 1986. Three cool-season forage grasses, intermediate wheatgrass, tall fescue, and smooth bromegrass, and two warm-season grasses, big bluestem and switchgrass, were included. The control of three major summer annual grasses, green foxtail, barnyardgrass, and large crabgrass, was excellent with fenoxaprop at 0.22 kg ai/ha. Slight to moderate injury to cool-season forage grasses and severe injury to warm-season grasses were evident. Sethoxydim at 0.22 kg ai/ha and haloxyfop at 0.11 kg ai/ha controlled green foxtail and large crabgrass, but not barnyardgrass. Sulfometuron-treated big bluestem and switchgrass plots had the best forage stand frequencies and yields and, at the rate used, sulfometuron satisfactorily controlled green foxtail but only marginally controlled barnyardgrass and large crabgrass.

Plots infested with quackgrass (Agropyron repens (L.) Beauv.) were treated with 2-chloro-4-ethylamino-6-isopropyl-s-triazine (atrazine) at several rates at various times and subjected to a number of cultural and cropping treatments. Depletion of carbohydrate reserves in the rhizomes increased with time after treatment. Recovery of the quackgrass occurred after 2 lb/A but usually not after 4 lb/A applications. Applications of nitrogen increased the rate of carbohydrate depletion. Two applications of atrazine at reduced rates were equal or superior to a single heavy rate. Tillage after treatment and crop competition improved the control of quackgrass obtained.

Amine salts of 2,4,5-trichlorophenoxy-propionic acid (silvex) and 2,4,5-trichlorophenoxyacetic acid (2,4,5-T) were applied to tall larkspur, Delphinium barbeyi Huth, at 2, 4, and 8 lb/A on three dates. Leaf and stem samples collected 1, 2, and 3 weeks after treatment yielded significantly higher concentrations of alkaloids than did controls. Leaves and stems from plants treated with silvex contained more alkaloids than did those treated with 2,4,5-T. Alkaloid concentration in the leaves varied directly with the rate of herbicide following the first treatment in mid-July, but this relation was not apparent in samples obtained from the third treatment in August.

Laboratory and field experiments were conducted to determine the effects of temperature, oxygen, and seed burial depth on woolly cupgrass seed dormancy. Woolly cupgrass seeds at physiological maturity are innately dormant. Stratifying these seeds at 5 C for 8 wk increased germination to greater than 90%, regardless of the germination temperature. Alternating the germination temperature hastened germination by 2 wk, while seedcoat removal hastened germination by another 4 wk. Low oxygen concentration was more detrimental to seed germination when seeds were subjected to constant temperatures in comparison to alternating temperatures. Oxygen concentration did not affect seed germination when seeds were placed in an alternating 15/25 C regime. Seed germination was approximately 15% less when seeds were stratified for 2 wk and subjected to oxygen concentrations below the ambient oxygen concentration, whereas this decrease was present only at the 8% oxygen concentration when seeds were stratified 4 wk. In the field, the stratification requirement was satisfied by early December for the study year. Seeds remaining on the soil surface overcame dormancy sooner than seeds buried 2 or 4 cm.

Glyphosate-resistant (GR) Palmer amaranth (Amaranthus palmeri S. Watson) is considered one of the most troublesome weeds in the southern and central United States, but results of previous research to determine the mode of inheritance of this trait have been conflicting and inconclusive. In this study, we examined segregation patterns of EPSPS gene-copy numbers in F1 and F2 generations of A. palmeri and found no evidence of a Mendelian single-gene pattern of inheritance. Transgressive segregation for copy number was exhibited by several F1 and all of the F2 families, most likely the product of EPSPS copy-number variation within each plant. This variation was confirmed by assaying gene-copy number across clonal generations and among individual shoots on the same plant, demonstrating that EPSPS amplification levels vary significantly within a single plant. Increases and decreases in copy number occurred in a controlled, stress-free environment in the absence of glyphosate, indicating that EPSPS gene amplification is a random and variable process within the plant. The ability of A. palmeri to gain or lose EPSPS gene copies is a valuable adaptive trait, allowing this species to respond rapidly to selection pressures and changing environments.

Biannual applications of hexazinone have been applied in many lowbush blueberry fields in Nova Scotia for more than 30 years. Persistent reliance on a single herbicide chemistry may have selected for hexazinone-resistant red sorrel. The recommended rate of hexazinone (1.92 kg ai ha−1) no longer controls red sorrel in many growing regions. Six levels of hexazinone (0, 0.48, 0.96, 1.92, 3.84, and 7.68 kg ai ha−1) were applied to red sorrel plants grown in a greenhouse from seeds collected from three commercial fields and a no blueberry area to determine if they were hexazinone resistant. Red sorrel from two sites where hexazinone had not been applied regularly died at the 0.96 kg ai ha−1 rate of hexazinone whereas red sorrel from two commercial fields survived at 7.68 kg ai ha−1. It is concluded that red sorrel is hexazinone-resistant in some wild blueberry fields. A portion of the psbA gene was sequenced and it was determined that resistant plants had a Phe to Val substitution at position 255 in the D1 protein. This is the first recorded instance of hexazinone resistance in a perennial broadleaf weed in blueberry fields.

Methiozolin is a new herbicide with an unknown mechanism of action (MOA) for control of annual bluegrass (Poa annua L.) in several warm- and cool-season turfgrasses. In the literature, methiozolin was proposed to be a pigment inhibitor via inhibition of tyrosine aminotransferases (TATs) or a cellulose biosynthesis inhibitor (CBI). Here, exploratory research was conducted to characterize the herbicide symptomology and MOA of methiozolin. Arabidopsis (Arabidopsis thaliana L.) and P. annua exhibited a similar level of susceptibility to methiozolin, and arrest of meristematic growth was the most characteristic symptomology. For example, methiozolin inhibited A. thaliana root growth (GR50 8 nM) and shoot emergence (GR80 ˜50 nM), and apical meristem growth was completely arrested at rates greater than 500 nM. We concluded that methiozolin was neither a TAT nor a CBI inhibitor. Methiozolin had a minor effect on chlorophyll and alpha-tocopherol content in treated seedlings (<500 nM), and supplements in the proposed TAT pathway could not lessen phytotoxicity. Examination of microscopic images of roots revealed that methiozolin-treated (100 nM) and untreated seedlings had similar root cell lengths. Thus, methiozolin inhibits cell proliferation and not elongation from meristematic tissue. Subsequently, we suspected methiozolin was an inhibitor of the mevalonic acid (MVA) pathway, because its herbicidal symptomologies were nearly indistinguishable from those caused by lovastatin. However, methiozolin did not inhibit phytosterol production, and MVA pathway metabolites did not rescue treated seedlings. Further experiments showed that methiozolin produced a physiological profile very similar to cinmethylin across a number of assays, a known inhibitor of fatty-acid synthesis through inhibition of thioesterases (FATs). Experiments with lesser duckweed (Lemna aequinoctialis Welw.; syn. Lemna paucicostata Hegelm.) showed that methiozolin also reduced fatty-acid content in Lemna with a profile similar, but not identical, to cinmethylin. However, there was no difference in fatty-acid content between treated (1 µM) and untreated A. thaliana seedlings. Methiozolin also bound to both A, thaliana and L. aequinoctialis FATs in vitro. Modeling suggested that methiozolin and cinmethylin have comparable and overlapping FAT binding sites. While there was a discrepancy in the effect of methiozolin on fatty-acid content between L. aequinoctialis and A. thaliana, the overall evidence indicates that methiozolin is a FAT inhibitor and acts in a similar manner as cinmethylin.

Herbicide resistance within key driver weeds, such as common waterhemp [Amaranthus tuberculatus (Moq.) Sauer var. rudis (Sauer) Costea and Tardif ], constrains available management options for crop production. Routine surveillance for herbicide resistance provides a mechanism to monitor the development and spread of resistant populations over time. Furthermore, the identification and quantification of resistance mechanisms at the population level can provide information that helps growers develop effective management plans. Populations of Amaranthus spp., including A. tuberculatus, redroot pigweed (Amaranthus retroflexus L.), and Palmer amaranth (Amaranthus palmeri S. Watson), were collected from 51 fields in Ohio during the 2016 growing season. Twenty-four A. tuberculatus populations were screened for resistance to the herbicides lactofen, atrazine, and glyphosate. Phenotypically resistant plants were further investigated to determine the frequency of known resistance mechanisms. Resistance to lactofen was infrequently observed throughout the populations, with 8 of 22 populations exhibiting resistant plants. Within those eight resistant populations, the ΔG210 resistance mechanism was observed in 17 of 30 phenotypically resistant plants, and the remainder lacked all known resistance mechanisms. Resistance to atrazine was observed in 12 of 15 populations; however, a target-site resistance mechanism was not observed in these populations. Resistance to glyphosate was observed in all populations. Gene amplification was the predominant glyphosate-resistance mechanism (147 of 322 plants) in the evaluated populations. The Pro-106-Ser mutation was identified in 24 plants, half of which also possessed gene amplification. In this study, molecular screening generally underestimated the phenotypically observed resistance. Continued mechanism discovery and marker development is required for improved detection of herbicide resistance through molecular assays.