Effects of Rainfall on Foliar Herbicides Applied to Seedling Johnsongrass (Sorghum halepense)

1988 ◽  
Vol 2 (2) ◽  
pp. 153-158 ◽  
Author(s):  
Charles T. Bryson
Keyword(s):  
Propionic Acid ◽  
Phosphonic Acid ◽  
Sorghum Halepense ◽  
Propanoic Acid ◽  
Herbicide Application ◽  
Time Intervals ◽  
Greenhouse Experiments ◽  
Acid Herbicides

The effects of rainfall on the efficacy of 11 foliar-applied herbicides were evaluated for their control of seedling johnsongrass [Sorghum halepense (L.) Pers. # SORHA] in greenhouse experiments during 1984 and 1985 at Stoneville, MS. Time intervals between herbicide application and rainfall (at 1.27 cm in 10 ± 0.5 min) ranged from 5 to 60 and 30 to 240 min depending on herbicide classification. In general, the phosphonic acid herbicides glyphosate [N-(phosphonomethyl)glycine] and SC-0224 (trimethylsulfonium carboxymethylaminomethylphosphonate) at 0.99 kg ai/ha required rain-free periods ≥240 min to control seedling johnsongrass effectively. The selective postemergence grass herbicides generally required ≥60 min to control seedling johnsongrass effectively when control without rainfall was ≥85%. Among the selective herbicides tested, haloxyfop {2-[4-[[3-chloro-5-(trifluoromethyl)-2-pyridinyl]oxy] phenoxy] propanoic acid} and DPX-Y6202 {ethyl[2-[4-(6-chloro-2-quinoxalinyl)oxy] phenoxy] propionic acid} at 0.06 kg ae/ha required the shortest time between herbicide application and rainfall to be effective. As herbicide rates were reduced, the effects of rainfall increased.

Effects of Rainfall on Foliar Herbicides Applied to Rhizome Johnsongrass

Weed Science ◽  
1987 ◽  
Vol 35 (1) ◽  
pp. 115-119 ◽  
Author(s):  
Charles T. Bryson
Keyword(s):  
Sorghum Halepense ◽  
Propanoic Acid ◽  
Herbicide Application ◽  
Time Intervals ◽  
Rainfall Simulator ◽  
Greenhouse Experiments ◽  
Time Periods ◽  
Control Equivalent

A rainfall simulator was used to evaluate the effects of washoff on 10 foliar-applied herbicides on johnsongrass [Sorghum halepense(L.) Pers. # SORHA] in greenhouse experiments during 1983 and 1984 at Stoneville, MS. Time intervals between herbicide application and rainfall ranged from 20 to 240 min. Johnsongrass topgrowth control was equivalent to rain-free treatments using DPX-Y6202 {ethyl [2-[4-(6-chloro-2-quinozalinyl)oxy] phenoxy] propionate} at 0.03 and 0.06 kg/ha at time periods of 90 and 40 min between herbicide application and rainfall, respectively, at 28 days after treatment (DAT). A period of 120 min was required for johnsongrass control equivalent to rain-free treatments using sethoxydim {2-[1-(ethoxyimino)butyl]-5-[2-(ethylthio)propyl]-3-hydroxy-2-cyclohexen-1-one} at 0.06 kg/ha, haloxyfop {2-[4-[[3-chloro-5-(trifluoromethyl)-2-pyridinyl]oxy] phenoxy] propanoic acid} at 0.03 and 0.06 kg/ha, and cloproxydim {(E,E-2-[1-[[(3-chloro-2-propenyl)oxy] imino] butyl]-5-[2-ethylthio)propyl]-3-hydroxy-2-cyclohexen-1-one} at 28 DAT. Neither glyphosate [N-(phosphonomethyl)glycine] and SC-0224 (trimethylsulfoniumcarboxy methylaminomethylphosphonate) at 0.45 and 0.99 kg/ha nor other selective herbicides at 0.03 and 0.06 kg/ha gave equivalent johnsongrass topgrowth control to rain-free treatments when rainfall occurred within 240 and 120 min, respectively.

scholarly journals Sulfentrazone efficiency on Ipomoea hederifolia and Ipomoea quamoclit as influenced by rain and sugarcane straw

2013 ◽  
Vol 31 (1) ◽  
pp. 165-174 ◽  
Author(s):  
N.M Correia ◽  
E.H Camilo ◽  
E.A Santos
Keyword(s):  
Field Experiment ◽  
Biological Effects ◽  
Soil Surface ◽  
Time Interval ◽  
Herbicide Application ◽  
Time Intervals ◽  
Greenhouse Experiments ◽  
Sugarcane Straw ◽  
Simulated Rain ◽  
Rain Simulation

The aim of this study was to assess the capacity of sulfentrazone applied in pre-emergence in controlling Ipomoea hederifolia and Ipomoea quamoclit as a function of the time interval between herbicide application and the occurrence of rain, and the presence of sugarcane straw on the soil surface. Two greenhouse experiments and one field experiment were conducted. For the greenhouse experiments, the study included three doses of sulfentrazone applied by spraying 0, 0.6, and 0.9 kg ha-1, two amounts of straw on the soil (0 and 10 t ha-1), and five time intervals between the application of herbicide and rain simulation (0, 20, 40, 60, and 90 days). In the field experiment, five herbicide treatments (sulfentrazone at 0.6 and 0.9 kg ha-1, sulfentrazone + hexazinone at 0.6 + 0.25 kg ha-1, amicarbazone at 1.4 kg ha-1, and imazapic at 0.147 kg ha-1) and two controls with no herbicide were studied. Management conditions with or without sugarcane straw on the soil were also assessed. From the greenhouse experiments, sulfentrazone application at 0.6 kg ha-1 was found to provide for the efficient control of I. hederifolia and I. quamoclit in a dry environment, with up to 90 days between herbicide application and rain simulation. After herbicide application, 20 mm of simulated rain was enough to leach sulfentrazone from the straw to the soil, as the biological effects observed in I. hederifolia and I. quamoclit remained unaffected. Under field conditions, either with or without sugarcane straw left on the soil, sulfentrazone alone (0.6 or 0.9 kg ha-1) or sulfentrazone combined with hexazinone (0.6 + 0.25 kg ha-1) was effective in the control of I. hederifolia and I. quamoclit, exhibiting similar or better control than amicarbazone (1.4 kg ha-1) and imazapic (0.147 kg ha-1).

The Effect of Surfactant and Environment on the Toxicity of Metriflufen to Soybeans (Glycine max) and Johnsongrass (Sorghum halepense)

Weed Science ◽  
1979 ◽  
Vol 27 (6) ◽  
pp. 675-679 ◽  
Author(s):  
C. G. McWhorter
Keyword(s):  
Glycine Max ◽  
Methyl Ester ◽  
Relative Humidity ◽  
Air Temperature ◽  
Sorghum Halepense ◽  
Growth Chamber ◽  
Propanoic Acid ◽  
Herbicide Treatment ◽  
Over The Top

Metriflufen {2-[4-(4-trifluoromethylphenoxy)phenoxy] propanoic acid} was applied as the methyl ester at 0.28 and 0.56 kg/ha over-the-top to johnsongrass [Sorghum halepense(L.) Pers.] growing from rhizomes and to soybeans [Glycine max(L.) Merr. ‘Lee 68′]. After herbicide treatment, plants were grown in the growth chamber for 14 days at 16, 24, or 32 C with relative humidity (RH) at 40 or 100% at each air temperature. Johnsongrass was not controlled at 16 C regardless of metriflufen rate, RH, or the addition of nonoxynol [α-(p-nonylphenyl)-ω-hydroxypoly (oxyethylene)] (with 9.5 moles of polyoxyethylene) surfactant at 0.25 (g/100 ml) to spray solutions. Johnsongrass control at 24 C varied from 5 to 98%, with significantly better control at 100% than at 40% RH. The presence of surfactant increased johnsongrass control at 24 C and 40% RH but not at 24 C and 100% RH. Johnsongrass control at 32 C varied from 48 to 98%, and it was not increased by the presence of the surfactant, regardless of metriflufen rate or RH level. At 16 C metriflufen was more injurious to soybeans than to johnsongrass, but at 24 and 32 C johnsongrass control was significantly greater than soybean injury. The presence of surfactant in spray solutions generally did not increase soybean injury, regardless of temperature or RH level. These results suggest that metriflufen is most selective in controlling johnsongrass in soybeans at 24 C, especially under high RH.

Investigations into the Growth Suppressing Effect of Nicosulfuron-Treated Johnsongrass (Sorghum halepense) on Corn (Zea mays)

Weed Science ◽  
1996 ◽  
Vol 44 (3) ◽  
pp. 640-644 ◽  
Author(s):  
Nagabhushana G. Gubbiga ◽  
A. Douglas Worsham ◽  
Frederick T. Corbin
Keyword(s):  
Soil Surface ◽  
Root Systems ◽  
Application Rate ◽  
Growth And Yield ◽  
Sorghum Halepense ◽  
Growth Reduction ◽  
Herbicide Application ◽  
Stunted Growth ◽  
Rooting Medium ◽  
Excellent Control

Greenhouse and growth chamber experiments were conducted to determine the reasons for stunted growth and yield suppression of corn noticed sometimes in nicosulfuron-treated corn fields infested with heavy population of johnsongrass. Results indicated that in the absence of johnsongrass, nicosulfuron applied broadcast POST at 35 g ai ha−1had no effect on corn. However, growth reduction of corn occurred when nicosulfuron-treated johnsongrass and corn were allowed to share the same rooting medium with their root systems intermingled. The reduction in growth was even greater when corn foliage or the soil surface were also treated with johnsongrass. The extent of growth reduction of corn growing with nicosulfuron-killed johnsongrass depended on weed density and herbicide application rate. Greater growth reductions occurred at four johnsongrass plants per pot compared to two and at a higher application rate of 100 μg nicosulfuron per plant. In general, johnsongrass killed by nicosulfuron appeared to be more phytotoxic to corn than plants killed by paraquat. Nicosulfuron provided excellent control of johnsongrass and improved corn growth by two to three times that of not controlling johnsongrass, but it could not elevate corn growth to the level obtained when johnsongrass was controlled by paraquat or in the absence of interference from johnsongrass.

Effects of Herbicide Application Timing on Johnsongrass (Sorghum halepense) and Pitted Morningglory (Ipomoea lacunosa) Control

1990 ◽  
Vol 4 (4) ◽  
pp. 900-903 ◽  
Author(s):  
David R. Shaw ◽  
Sunil Ratnayake ◽  
Clyde A. Smith
Keyword(s):  
Growth Stage ◽  
Field Experiments ◽  
Sorghum Halepense ◽  
Herbicide Application ◽  
Ipomoea Lacunosa ◽  
Application Timing ◽  
Final Treatment ◽  
Pitted Morningglory

Field experiments were conducted to evaluate the influence of application timing of imazethapyr and fluazifop-P on rhizome johnsongrass and pitted morningglory control in soybean. Herbicides were applied at three timings keyed to johnsongrass heights of 15, 30, and 60 cm and 3-, 6-, and 9-leaf pitted morningglory. Evaluations 6 wk after the final treatment indicated imazethapyr controlled both species best when applied at the 15-cm johnsongrass growth stage. Increasing imazethapyr rate did not increase control of pitted morningglory, but did increase johnsongrass control at the 15-cm application timing. However, at the 30-cm johnsongrass application timing, increasing the rate from 0.07 to 0.10 kg ha-1improved control of both species. Johnsongrass control with imazethapyr was no more than 64% when applications were delayed to 30-cm or larger johnsongrass. Fluazifop-P controlled johnsongrass well at all timings.

scholarly journals Purification and Characterization of Two Enantioselective α-Ketoglutarate-Dependent Dioxygenases, RdpA and SdpA, from Sphingomonas herbicidovorans MH

2006 ◽  
Vol 72 (7) ◽  
pp. 4853-4861 ◽  
Author(s):  
Tina A. Müller ◽  
Thomas Fleischmann ◽  
Jan Roelof van der Meer ◽  
Hans-Peter E. Kohler
Keyword(s):  
Amino Acids ◽  
Divalent Cations ◽  
Propanoic Acid ◽  
Dichlorophenoxyacetic Acid ◽  
Purification And Characterization ◽  
Subgroup Ii ◽  
2,4 Dichlorophenoxyacetic Acid ◽  
Acid Herbicides ◽  
Growth Experiments

ABSTRACT α-Ketoglutarate-dependent (R)-dichlorprop dioxygenase (RdpA) and α-ketoglutarate-dependent (S)-dichlorprop dioxygenase (SdpA), which are involved in the degradation of phenoxyalkanoic acid herbicides in Sphingomonas herbicidovorans MH, were expressed and purified as His6-tagged fusion proteins from Escherichia coli BL21(DE3)(pLysS). RdpA and SdpA belong to subgroup II of the α-ketoglutarate-dependent dioxygenases and share the specific motif HXDX24TX131HX10R. Amino acids His-111, Asp-113, and His-270 and amino acids His-102, Asp-104, and His 257 comprise the 2-His-1-carboxylate facial triads and were predicted to be involved in iron binding in RdpA and SdpA, respectively. RdpA exclusively transformed the (R) enantiomers of mecoprop [2-(4-chloro-2-methylphenoxy)propanoic acid] and dichlorprop [2-(2,4-dichlorophenoxy)propanoic acid], whereas SdpA was specific for the (S) enantiomers. The apparent Km values were 99 μM for (R)-mecoprop, 164 μM for (R)-dichlorprop, and 3 μM for α-ketoglutarate for RdpA and 132 μM for (S)-mecoprop, 495 μM for (S)-dichlorprop, and 20 μM for α-ketoglutarate for SdpA. Both enzymes had high apparent Km values for oxygen; these values were 159 μM for SdpA and >230 μM for RdpA, whose activity was linearly dependent on oxygen at the concentration range measured. Both enzymes had narrow cosubstrate specificity; only 2-oxoadipate was able to replace α-ketoglutarate, and the rates were substantially diminished. Ferrous iron was necessary for activity of the enzymes, and other divalent cations could not replace it. Although the results of growth experiments suggest that strain MH harbors a specific 2,4-dichlorophenoxyacetic acid-converting enzyme, tfdA-, tfdAα-, or cadAB-like genes were not discovered in a screening analysis in which heterologous hybridization and PCR were used.

scholarly journals Crystal Packing and Supramolecular Motifs in Four Phenoxyalkanoic Acid Herbicides—Low-Temperature Redeterminations

2011 ◽  
Vol 2011 ◽  
pp. 1-5 ◽  
Author(s):  
Lesław Sieroń ◽  
Joanna Kobyłecka ◽  
Anna Turek
Keyword(s):  
Low Temperature ◽  
Propionic Acid ◽  
Crystal Packing ◽  
Dichlorophenoxyacetic Acid ◽  
X Ray ◽  
Π Interactions ◽  
X Ray Crystallography ◽  
Supramolecular Motifs ◽  
2,4 Dichlorophenoxyacetic Acid ◽  
Acid Herbicides

A low-temperature redetermination by X-ray crystallography of four phenoxyalkanoic acid herbicides, 4-chloro-2-methylphenoxyacetic acid (MCPA), rac-2-(4-chloro-2-methylphenoxy)propionic acid (MCPP), 2,4-dichlorophenoxyacetic acid (2,4-D), and 2,4-dichlorophenoxybutyric acid (2,4-DB), allowed the supramolecular structures of these compounds to be precisely described in terms of C⋯O/C–H⋯π interactions. The geometric parameters of the redetermined structures agree with those previously reported, but with improved precision.

scholarly journals Fenoxaprop Activity Influenced by Auxin-like Herbicide Application Timing

HortScience ◽  
1994 ◽  
Vol 29 (12) ◽  
pp. 1518-1519 ◽  
Author(s):  
P.H. Dernoeden ◽  
M.A. Fidanza
Keyword(s):  
Acetic Acid ◽  
Ethyl Ester ◽  
No Reduction ◽  
Propanoic Acid ◽  
Annual Grass ◽  
Herbicide Application ◽  
Application Timing ◽  
Before And After ◽  
Dichlorophenoxy Acetic Acid ◽  
Methoxybenzoic Acid

Fenoxaprop is used on turfgrasses to control smooth crabgrass [Digitaria ischaemum (Schreb. ex Sweib.) Schreb. ex Muhl.] and other annual grass weeds. Our objective was to determine if a broadleaf weed herbicide (BWH = 2,4-D + mecoprop + dicamba) would affect fenoxaprop activity. The BWH was applied several days or weeks before and after fenoxaprop was applied. Smooth crabgrass control by fenoxaprop was reduced significantly when the BWH was applied ≤14 days before fenoxaprop was applied. Extremely poor crabgrass control occurred when fenoxaprop was tank-mixed with the BWH. There was no reduction in crabgrass control when the BWH was applied 21 days before or ≥3 days after fenoxaprop. Chemical names used: ethyl ester of (±)-2-[4-[(6-chloro-2-benzoxazolyl)oxy]phenoxy]propanoic acid (fenoxaprop); 2,4-dichlorophenoxy acetic acid (2,4-D); (+)-2-(4-chloro-2-methylphenoxy)propanoic acid (mecoprop); 3,6-dichloro-2-methoxybenzoic acid (dicamba).

Soybean (Glycine max) Competition Helps Herbicides Control Johnsongrass (Sorghum halepense)

1988 ◽  
Vol 2 (1) ◽  
pp. 46-48 ◽  
Author(s):  
Leo E. Bendixen
Keyword(s):  
Glycine Max ◽  
Sorghum Halepense ◽  
Propanoic Acid ◽  
Pentanoic Acid ◽  
Postemergence Herbicides

Six postemergence herbicides were applied two consecutive years in single and split applications to compare johnsongrass [Sorghum halepense(L.) Pers. # SORHA] control in soybeans [Glycine max(L.) Merr.] planted in 25- and 76-cm inter-row spacings. Significantly less johnsongrass existed at harvest in the 25-cm spacings than in the 76-cm spacings with split applications of fenoxaprop {(±)-2-[4-[(6-chloro-2-benzoxazolyl)oxy] phenoxy] propanoic acid} at 100 g ae/ha, fluazifop {(±)-2-[4-[[5-(trifluoromethyl)-2-pyridinyl] oxy] phenoxy] propanoic acid} at 100 g ae/ha, sethoxydim {2-[1-(ethoxyimino)butyl]-5-[2-(ethylthio)propyl]-3-hydroxy-2-cyclohexen-1-one} at 200 g ai/ha, and SC-1084 {3-hydroxy-4-[4-[[5-(trifluoromethyl)-2-pyridinyl] oxy] phenoxy] pentanoic acid} at 250 g ae/ha. Quizalofop {(±)-2-[4-[(6-chloro-2-quinoxalinyl)oxy] phenoxy] propanoic acid} at 70 g ae/ha and haloxyfop {2-[4-[[3-chloro-5-(trifluoromethyl)-2-pyridinyl] oxy] phenoxy] propanoic acid} at 100 g ae/ha controlled johnsongrass so well that differences between the two row spacings were not significant.

Fatty-acid biosynthesis and acetyl-coa carboxylase as a target of diclofop, fenoxaprop and other aryloxy-phenoxy-propionic acid herbicides

1988 ◽  
Vol 43 (1-2) ◽  
pp. 47-54 ◽  
Author(s):  
Klaus Kobek ◽  
Manfred Focke ◽  
K. Lichtenthaler Botanisches
Keyword(s):  
Fatty Acid ◽  
Propionic Acid ◽  
Fatty Acid Biosynthesis ◽  
De Novo ◽  
Free Acid ◽  
Acetate Incorporation ◽  
Acetyl Coa Carboxylase ◽  
Acid Biosynthesis ◽  
Acetyl Coa ◽  
Acid Herbicides

The effect of the herbicides and aryloxy-phenoxy-propionic acid derivatives diclofop, fenoxaprop, fluazifop and haloxyfop and their ethyl, methyl or butyl esters on the de novo fatty-acid biosynthesis of isolated chloroplasts was investigated with intact chloroplasts isolated from sensitive grasses (Poaceae) and tolerant dicotyledonous plants (Pisum, Spinacia). The 4 herbicides (free-acid form) block the de novo fatty-acid biosynthesis ([2-14C]acetate incorporation into the total fatty-acid fraction) of the sensitive Avena chloroplasts in a dose-dependent manner. The I50- values (a 50% inhibition of the [14C]acetate incorporation) lie in the range of 10-7 to 2 x 10-6 ᴍ. The ethyl or methyl esters (diclofop, fenoxaprop, haloxyfop) and butyl ester (fluazifop) do not affect the de novo fatty-acid biosynthesis of isolated chloroplasts or only at a very high concentration of ca. 10-4 ᴍ. In contrast, the de novo fatty-acid biosynthesis of the tolerant dicotyledonous species (pea, spinach) is not affected by the 4 aryloxy-phenoxy-propionic acid herbicides. In an enzyme preparation isolated from chloroplasts of the herbicide-sensitive barley plants the de novo fatty-acid biosynthesis from [14C]acetate and [14C]acetyl-CoA is blocked by all 4 herbicides (free acids), whereas that of [14C]malonate and [14C]malonyl-CoA is not affected. This strongly suggests that the target of all 4 herbicides (free-acid form) is the acetyl-CoA carboxylase within the chloroplasts. The applied ester derivatives, in turn, which are ineffective in the isolated chloroplast test system, have equally little or no effect on the activity of the acetyl-CoA carboxylase. It is assumed that the acetyl-CoA carboxylase of the tolerant dicot plants investigated is modified in such a way that the 4 herbicides cannot bind to and affect the target

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