Laboratory and greenhouse studies were conducted to evaluate the effects of chemical treatments applied to Palmer amaranth seeds or gynoecious plants that retain seeds to determine seed germination and quality. Treatments applied to physiologically mature Palmer amaranth seed included acifluorfen, dicamba, ethephon, flumioxazin, fomesafen, halosulfuron, linuron, metribuzin, oryzalin, pendimethalin, pyroxasulfone, S-metolachlor, saflufenacil, trifluralin, and 2,4-D plus crop oil concentrate applied at 1× and 2× the suggested use rates from the manufacturer. Germination was reduced by 20% when 2,4-D was used, 15% when dicamba was used, and 13% when halosulfuron and pyroxasulfone were used. Use of dicamba, ethephon, halosulfuron, oryzalin, trifluralin, and 2,4-D resulted in decreased seedling length by an average of at least 50%. Due to the observed effect of dicamba, ethephon, halosulfuron, oryzalin, trifluralin, and 2,4-D, these treatments were applied to gynoecious Palmer amaranth inflorescence at the 2× registered application rates to evaluate their effects on progeny seed. Dicamba use resulted in a 24% decrease in seed germination, whereas all other treatment results were similar to those of the control. Crush tests showed that seed viability was greater than 95%, thus dicamba did not have a strong effect on seed viability. No treatments applied to Palmer amaranth inflorescence affected average seedling length; therefore, chemical treatments did not affect the quality of seeds that germinated.

Timely results from whole-plant, herbicide-resistant weed screenings are crucial to heighten grower awareness. However, the high degree of physiological dormancy of giant ragweed (Ambrosia trifida L.) seed exacerbates this process. The most effective methods for alleviating dormancy, to date, are either labor-intensive (embryo excision) or require several weeks (soil stratification). This research describes a conditioning process involving clipping and aeration of seed in water that is highly effective at alleviating dormancy and requires less skill and time compared with previous techniques. Ambrosia trifida seeds were collected over 2 yr at two different collection timings (September 25, “early”; October 25, “late”), subjected to various treatments intended to release dormancy, and evaluated for emergence over 18 d in the greenhouse. The use of germination-promoting chemicals (ethephon, gibberellic acid, and thiourea) generally provided no increase in emergence compared with water and occasionally produced seedlings with abnormal growth unsuitable for further experimentation. Conditioning yielded between 30% and 33% emergence for both early and late collections of seeds with no afterripening period compared with 0% emergence for seeds imbibed in water. Following an 8-wk period of dry storage at 4 C, conditioning yielded nearly 80% emergence for both collection timings, while emergence of seeds imbibed in water was 10% and 27% for early and late collections, respectively. Soil stratification in moist soil for 8 wk at 4 C was the second most effective treatment, yielding 46% to 49% emergence across both collections. Parameters of the Weibull function further indicated the conditioning treatment had the fastest rate of emergence and shortest lag phase between planting and first emergence. Methods to germinate A. trifida without an afterripening period have previously been unsuccessful. Therefore, the seed-conditioning method outlined in this work will be useful in expediting the confirmation of herbicide-resistant A. trifida incidences.

Field studies were conducted to determine the influence of herbicides on the development of internal necrosis (IN) in sweetpotato storage roots. In a slip propagation study, herbicide treatments included PRE application (immediately after covering seed roots with soil) of clomazone (0.42, 0.84 kg ai ha-1), flumioxazin (0.11, 0.21 kg ai ha-1), fomesafen (0.28, 0.56 kg ai ha-1), linuron (0.56, 1.12 kg ai ha-1), S-metolachlor (0.8, 1.6 kg ai ha-1), flumioxazin plus S-metolachlor (0.11 + 0.8 or 1.6 kg ha-1), and napropamide (1.12, 2.24 kg ai ha-1), and POST application (2 to 4 wk prior to cutting slips) of ethephon (0.84, 1.26 kg ai ha-1) and paraquat (0.14, 0.28 kg ai ha-1). In a field production study, flumioxazin, fomesafen, linuron, and paraquat were applied PREPLANT (one d prior to sweetpotato transplanting), clomazone, S-metolachlor, and napropamide were applied PRE [4 d after transplanting (DAP)], flumioxazin PREPLANT followed by (fb) S-metolachlor PRE, and ethephon applied POST (2 wk prior to harvest). Herbicide rates were similar to those used in the slip propagation study. Yield of sweetpotato in both studies was not affected by herbicide treatment. In both studies, IN incidence and severity increased with time and was greatest at 60 d after curing. No difference was observed between herbicide treatments for IN incidence and severity in the slip production study which indicates herbicide application at time of slip propagation does not impact the development of IN. In the field production study, the only treatment that increased IN incidence compared to the nontreated was ethephon with 53% and 2.3 incidence and severity, respectively. The presence of IN affected roots in nontreated plots indicates that some other pre- or post-curing factors other than herbicides are responsible for the development of IN. However, the ethephon application prior to sweetpotato root harvest escalates the development of IN.

The addition of chlorflurenol (methyl 2-chloro-9-hydroxyfluorene-9-carboxylate) at 0.6 kg ai/ha or mefluidide {N-[2,4-dimethyl-5-[[(trifluoromethyl)sulfonyl]amino]phenyl] acetamide} at 0.3 kg ai/ha to picloram (4-amino-3,5,6-tricloropicolinic acid) at 0.3 kg ae/ha increased leafy spurge (Euphorbia esula L. # EPHES) control compared to picloram alone. Application of 84 kg/ha nitrogen in the fall prior to a spring treatment of 0.3 kg/ha picloram decreased the original stand (75%) compared to no nitrogen (18%). In greenhouse experiments, chlorflurenol and mefluidide increased the amount of 14C-picloram absorbed approximately twofold when applied in combination but not when applied independently. Based on 14C-picloram absorbed, chlorflurenol and mefluidide each increased the amount of 14C translocated to the root system, whether applied independently or in combination with picloram. An increase in root bud numbers was observed following an application of 0.6 kg/ha chlorflurenol or nitrogen.

The effect of various growth regulators on seedling field bindweed (Convolvulus arvensis L. # CONAR) growth and control with herbicides was evaluated. Fourteen growth regulators were applied at 0.38 to 380 g/ha 7 days before herbicide application in greenhouse, growth chamber and field studies. Field bindweed seedlings pretreated with growth regulators were more effectively controlled by herbicides compared to those not pretreated in greenhouse evaluations. Abscisic acid [[R-(Z,E)]-(+)-5-(1-hydroxy-2,6-6-trimethyl-4-oxo-2-cyclohexane-1-yl)-3-methyl-2,4-pentadicenoic acid] (ABA), ancymidol [a-cyclopropyl-a-(p-methoxyphenyl)-5-pyrimidine methanol], cycloheximide {3-[2-(3,5-dimethyl-2-oxocylohexyl)-2-hydroxyethyl]glutarimide}, ethylenediamine tetraacetic acid [N,N′-1,2-ethanediyl-bis-(N-(carboxymethyl) glycine] (EDTA), and 1-naphthaleneacetic acid (NAA) increased field bindweed stem length. Ancymidol and gibberellic acid [ent-3α,10,13-trihydroxy-20-norgibberell-1,16-diene-7,19-dioc acid 19,10-lactone] (GA) increased root weight, and GA increased root length. Cycloheximide, ethephon [(2-chloroethyl)phosphonic acid] and MH (1,2-dihydro-3,6-pyridazinedione) decreased field bindweed root weight. Ancymidol, GA and IAA (indole-3-acetic acid) increased the number of shoots per plant of seedling field bindweed. Dicamba (3,6-dichloro-2-methoxybenzoic acid) efficacy was enhanced following field bindweed preconditioning with ethephon and IAA. Ancymidol and cycloheximide applied as pretreatments increased glyphosate [N-(phosphonomethyl)glycine] activity on seedling field bindweed. Ancymidol and IAA pretreatment improved field bindweed control with triclopyr {[(3,5,6-trichloro-2-pyridinyl)oxy] acetic acid}. Herbicide-growth regulator combination treatments that increased field bindweed control in greenhouse and growth chamber studies did not increase top growth control in the field.

Field studies were conducted at the Main Experiment Station, Fayetteville, AR, in 1994 and 1995 to evaluate the effect of postemergence herbicides applied at late-season timings on sicklepod seed production and viability. AC 263,222, dicamba, glyphosate, glufosinate, and paraquat were applied at five rates (zero; labeled rate; one-half, one-fourth, and one-eighth the labeled rate) to three sicklepod growth stages (bud formation, flowering to 9-cm pods, and 15- to 30-cm pods). The greatest reduction in seed production occurred when herbicides were applied at the flowering to 9-cm pod growth stage. All herbicides applied at one-half the labeled rate to sicklepod at bud formation and at the flowering to 9-cm pod growth stage reduced seed production greater than 80%, except glufosinate. Regardless of herbicide, rate, or application timing, viability of remaining seed was ≥ 90% with all treatments.

Laboratory, greenhouse, and field experiments were conducted at the Lacombe Research Station to determine if CCC, ethephon, or CCC/ethephon had direct activity on quackgrass rhizome buds, and to determine if foliar applications of CCC/ethephon could predispose quackgrass to more effective control with sethoxydim. CCC, ethephon, and CCC/ethephon had growth regulating effects on the axillary buds and the apex of detached quackgrass rhizomes. CCC increased rhizome bud sprouting on rhizomes with the apex excised, but not on rhizomes with an intact apex. Ethephon or CCC/ethephon inhibited bud sprouting on rhizomes with an intact or excised apex. CCC/ethephon, but not CCC or ethephon alone, increased rhizome elongation on rhizomes with intact apices. In the greenhouse, pretreatments of CCC/ethephon increased sethoxydim activity on quackgrass rhizome buds and caused lower shoot emergence from one-bud rhizome segments. Results of field experiments were less consistent than those in the greenhouse. However, sometimes CCC or CCC/ethephon pretreatments resulted in increased quackgrass control in the field with sethoxydim.

A red fescue (Festuca rubra L.)- Kentucky bluegrass (Poa pratensis L.) turf was treated annually with amidochlor {N-[(acetylamino)methyl]-2-chloro-N-(2,6-diethylphenyl)acetamide} at 2.2, 2.8, and 3.4 kg ai/ha, mefluidide {N-[2,4-dimethyl-5-[[(trifluoromethyl)sulfonyl] amino] phenyl] acetamide} at 0.4 kg ai/ha, and ethephon [(2-chloroethyl) phosphonic acid] at 5.6 kg ai/ha for three consecutive years. Recuperative potential of treated turfgrass was determined in the field and in a greenhouse study. Amidochlor and mefluidide treatments injured turfgrass (11 to 64%) four weeks after application. However, turfgrass recovered after eight weeks. Amidochlor at 2.8 to 3.4 kg/ha and mefluidide at 0.4 kg/ha suppressed (75 to 100%) seedhead development. Ethephon at 5.6 kg/ha was ineffective. Turfgrass recovered normally each spring after amidochlor treatments, with no delay in spring green-up. Root length, root weight, and root:shoot weight ratio of the plugs from the greenhouse study were unaffected by three consecutive annual applications of amidochlor, mefluidide, and ethephon. One annual spring application of amidochlor, mefluidide, and ethephon for three consecutive years caused no adverse effects that would limit their use on red fescue-Kentucky bluegrass turf.

Dormant weed seeds are difficult to kill and, with the exception of soil sterilization methods, current weed control techniques are not effective against dormant weed seeds. This study was conducted to investigate the effects of temperature, light, soil moisture, burial depth, ethephon, and potassium nitrate (KNO3), and their interactions on the germination of false chamomile seeds under controlled conditions. False chamomile was photoblastic and thermophilic and germinated rapidly within the first 4 days of incubation under all conditions. Regression analysis indicated that ethephon and KNO3 had quadratic effects on false chamomile germination. Ethephon enhanced germination more than KNO3. There was a linear reduction in germination with increased storage time, and it is projected that zero germination should occur after 9 yr of storage at room temperature. Soil moisture had a positive linear effect and a positive interaction with ethephon on false chamomile germination. Very little germination occurred when seeds were buried 5 cm deep even with high soil moisture.

Germination stimulants were tested for effectiveness on velvetleaf seed imbibition and germination and concurrent microbial attack of seed to deplete weed seed in soil. Several chemicals increased in vitro seed germination and decreased the numbers of hard, viable seed. The proportion of nonviable seed, 5% with Fusarium oxysporum (Schlech.), was enhanced to 40% by adding ethephon at 100 μg/ml. Fungal density on seedling roots and imbibed (nonviable seed) was increased by chemical treatment. Seedling emergence was reduced 15% when ethephon or carbofuran was applied to soil with the fungus. Shoot dry weight decreased and root infection increased with all treatments regardless of fungal inoculation. Butylate and carbofuran increased infection of imbibed seed in soil by F. oxysporum while ethephon and AC94377 increased infection by other soil fungi.

Effects of ethylene and KNO3 on the germination of dormant common lambsquarters (Chenopodium album L. # CHEAL) seed were studied under controlled environmental conditions. Ethylene, applied in the gaseous form or as an aqueous solution of ethephon (2-chloroethylphosphonic acid), was able to overcome the dormancy of over 70% of the seed. The optimum concentrations of ethylene and ethephon were 10 μL·L-1 and 100 mg·L-1, respectively. The dormancy-breaking action of ethylene was dependent on the availability of nitrate. Hence, seed containing a high level of endogenous nitrate responded readily to ethylene, whereas nitrate-deficient seed required a combined application of ethylene and nitrate. Stimulation of seed germination by ethylene was observed in soil at all depths studied (up to 15 cm). The sensitivity of seed to ethylene increased upon imbibition to reach a peak on the third day, followed by a steady decline. Consequently, the greatest promotion of germination occurred when ethylene was administered during the first 3 to 4 days of imbibition. The loss of seed sensitivity was neither preempted nor overcome by an exogenous supply of KNO3, and may imply that the seed had passed into secondary dormancy. The present findings could form the basis for the use of ethylene to accomplish commercially significant promotion of germination in the field and thus improve the efficiency of the control of common lambsquarters.

In velvetleaf (Abutilon theophrasti Medic. ♯3 ABUTH), accelerated leaf abscission was a conspicuous response following foliar chlorsulfuron {2-chloro-N-[[(4-methoxy-6-methyl-1,3,5-triazin-2-yl)amino] carbonyl] benzenesulfonamide} treatment at 35 g ai/ha. Leaf abscission of treated plants was decreased by AVG [L-2-amino-4-(2-aminoethoxy)-trans-3-butenoic acid], an inhibitor of endogenous ethylene production. Chlorsulfuron stimulated ethylene production in the abscission zone and leaves of treated plants and also increased cellulase activity in the abscission zone. Accelerated leaf abscission of velvetleaf following chlorsulfuron application appears to result from chlorsulfuron-induced increases in endogenous ethylene production and cellulase activity.

Effects of ethylene, gibberellins, kinetin, nitrate, light, and temperature, each alone or combined with other factors, were studied on the germination of dormant seed of field pennycress (Thlaspi arvense L. # THLAR). Treated seed were incubated at a range of constant temperatures, at temperatures alternating daily between 12 and 22 C (12 h each), or at 12 C followed by transfer to 22 C. No germination ocurrred in water under any conditions. When applied in the dark KNO3 had no effect on germination under any of the temperature regimes. A combination of KNO3, light, and a shift in temperature from 12 to 22 C induced 100% germination. Four days of incubation at 12 C induced maximal seed sensitivity towards KNO3 + light, and the sensitivity remained unchanged if the incubation at 12 C was extended to 15 days. Upon transfer to 22 C, the effect of low-temperature incubation was lost within 3 days. Of the two seed lots studied, one had a relatively lower chilling requirement, but both had similar requirements for light and KNO3. Gibberellic acids4+7 (GA4+7) induced 100% germination in the dark or light at all temperature regimes. Gibberellic acid3 (GA3) was promotive under isothermal conditions, but its effectiveness was enhanced by a shift in temperature from 12 to 22 C. Kinetin or ethephon, each applied alone, had little effect on germination. Ethephon and GA3 together induced 100% germination.

Curly dock (Rumex crispus L.) seeds failed to germinate in the dark, but germinated readily in light at 15, 20, and 25C. A secondary dormancy was induced in these seeds by 6 days of dark or light incubation at 30C (thermodormancy), by 6 days of dark incubation at 15C, or by a prolonged soaking in −15.7 bar polyethylene glycol-6000 (PEG) solution at 15C in light. The secondary dormancy induced at 15C was partially removed by 2-chloroethylphosphonic acid (ethephon) in presence of light; however, when the dormancy was induced at 30C, an addition of gibberellin A4+7 (GA4+7) to ethephon was necessary for effective removal of the dormancy. The ability of growth regulators to remove the secondary dormancy induced by prolonged dark incubation at 15C decreased progressively in light as the duration of dark incubation increased. The water-potential studies indicate that the thermodormancy can be attributed, at least in part, to the inability of the embryonic cells to lower their water potential to a level sufficient to cause radicle protrusion.

Maximum germination of flodman thistle [Cirsium flodmanii (Rydb.) Arthur ♯3 CIRFL] occurred at alternating temperatures of 10 to 20 and 20 to 30 C. Seeds germinated (20%) in 1.7 M NaCl. Light was important in seed germination; however, its absence could be overcome by adding 8.6 × 10-5 M GA3 (gibberellic acid) to the germination medium. The greatest seedling emergence occurred when seeds were planted on the soil surface and was lower when seeds were buried at any depth in the soil. Osmotic potentials at −0.5 MPa and greater reduced germination, but 3% of the seeds germinated at −1.3 MPa. Flodman thistle seedlings tolerated average plant water potentials of −0.9 and −1.1 MPa, but they died when the water potential was decreased to −1.5 MPa. Flodman thistle seedlings 43 days old and with four true leaves resprouted after topgrowth removal. Regrowth was evident on 75% of the clipped plants 13 days after initial topgrowth removal. Flodman thistle rosettes spread more rapidly and rosette survival was enhanced more in a weed-free nursery than in a weedy pasture.

The role of ethylene in kochia injury following the application of dicamba and other auxinic herbicides is not known. Experiments were conducted to evaluate kochia response to ethylene generated within plant tissue and to quantify ethylene emission from kochia following dicamba application to determine if ethylene production could be used to differentiate between dicamba-susceptible (S) and dicamba-resistant (R) kochia accessions. Dicamba at 0.28 kg ha−1 and fluroxypyr at 0.28 kg ha−1 caused severe stem and petiole twisting within 6 h of application, with S kochia exhibiting a greater level of epinasty than R kochia and fluroxypyr causing more epinasty than dicamba. Fluroxypyr provided similar control of S and R kochia, but dicamba provided less control of R kochia than S kochia. Ethylene evolution in S kochia from ethephon at 1.1 kg ha−1 and dicamba at 0.28 kg ha−1 was similar, approximately 70 ng (g fresh weight)−1 h−1. Elevated ethylene concentration from as much as 2 kg ha−1 ethephon did not produce epinastic symptoms or other plant response in S or R kochia. Ethylene evolution following dicamba application increased with time up to 48 h after application and with increasing dicamba rate up to 0.56 kg ha−1, which were the end points of the research. Ethylene evolution from the S accession was 2.5 times that of the R accession averaged across dicamba rates and harvest times. The greatest difference in ethylene evolution between S and R accessions occurred 24 h after treatment at 0.14 kg ha−1 dicamba, with S kochia producing ethylene at 470%, compared with R kochia.

Chemical ripening of sugarcane is an important component to profitable sugar production in the United States as well as other sugarcane industries throughout the world. Harvesting of sugarcane often begins before the sugarcane reaches the desirable maturity level. This is especially true in the Louisiana sugarcane industry where the window for harvesting is limited because of the risk of freezing temperatures encountered in a temperate climate. Research on the application of chemicals, mostly of herbicide origin, to enhance sucrose accumulation (ripening) or limit flowering to conserve stored sucrose has been conducted for more than 60 yr. The only sugarcane ripener currently registered for use in the United States is glyphosate applied before harvest. The herbicide fluazifop is used as the primary ripener of sugarcane in South Africa. The herbicides glyphosate, fluazifop, and sulfometuron-methyl and the growth regulators ethephon and trinexapac-ethyl are registered for use in Brazil. There is a continuing need to evaluate sugarcane ripeners to increase the utility of currently registered ripeners and to find additional ripeners for use by sugarcane industries. The need for alternatives to glyphosate is especially critical before a glyphosate-tolerant sugarcane can be utilized to improve control of problematic weeds.

Introduction. Prunus amygdalus and P. webbii can be used as rootstocks for almond cultivars due to their adaptability to severe environmental conditions. However, the time required for seedlings to reach a suitable size for transplanting may take 1 to 3 years. Our study tested the effects of foliar application of growth regulators on the vegetative growth and carbohydrate accumulation in shoots and roots of these species. Materials and methods. Six-week-old seedlings were treated with gibberellic acid (GA3) (100 mg·L–1) alone or with GA3 followed by ethephon [(100 and 200) mg·L–1], or chlormequat chloride (CCC) [(500 and 1000) mg·L–1], or paclobutrazol (PBZ) [(500 and 1000) mg·L–1]. Results and discussion. Most levels of plant growth regulators significantly enhanced seedling growth. However, GA3 alone was most effective on stem height, leaf area, and shoot fresh and dry weights of both almond species. The thickest stems of P. amygdalus and P. webbii were obtained from the application of 100 mg GA3·L–1 followed by application of (1000 and 500) mg PBZ·L–1, respectively. In both species, PBZ significantly increased leaf chlorophyll content compared with the controls as well as with the other treatments. Application of GA3 alone on P. webbii and of GA3 followed by 100 mg ethephon·L–1 on P. amygdalus showed the highest root number, and root fresh and dry weights. High levels of soluble sugars and starch in the shoots and roots of both species were observed when GA3 application was followed by PBZ. Conclusion. These results demonstrated that application of plant growth regulators to the seedlings might be a useful way of enhancing growth of P. amygdalus and P. webbii and reducing the time and cost of seedling production.