Vol. 15—1961 - NorthEastern Weed Science Society

Vol. 15—1961 - NorthEastern Weed Science Society Vol. 15—1961 - NorthEastern Weed Science Society

08.06.2015 Views

.32. for plant height, weight, and rhizome weights. Six replicates were used ­ for each tr eatm ent, Test solutions were prepared by dispersing the wetting agent in water, and diluting to the required concentration" then adding unlabelled sodium dalapon to a concentration equivalent to 10 pounds to 60 gallons. A sample of 2_C 14 labelled sodium salt of dalapon having a specific activity of O.98 millicuries per millimole was used for the test. The oolution employed contained 1.35 mtcrocurtes per milliliter. An area 5 mm, by 50 rnrn, on the upper surface of the third leaf of each test plant was walled with lanolin. This area was then supported in a horizontal position, and flooded with one-half millilU'er of the proper dalapon-wetting agent solution. A two hundred lambda aliquot of the 2-C 14 labelled sodium dalapon solution was added to the wetting agent solution on leach leaf, after which the leaves were allowed to dry. It was thought that perhaps the herbicide might be retained by the lanolin ring" or that the wetting agents might affect such a retention. This was checked in the following manner. Lanolin rings were formed on thin glass cover slips, and the rings were then filled withdalapon-2-C 14 solutions in water and with various wetting agents. After standing for one hour, the cover slips were washed under running water for ,30 seconds. The cover slips were then broken with tweezers and dropped into vials of scin­ ­ tillation solvent. After shaking to dissolve the lanolin, the vials were counted and background counts were ~btained..Jt..w.as considered that the lanolin ring per se had no interaction with either the herbicide or the wetting agents used. After five days, the plants were dissected and the individual leaves, stem, rhizomes, and roots were cut with shears into one-half inch s egrn entc, The various parts, 'except 'for the treated leaves, ,,;iere ground in a glass homogeniz er-, The pieces of treated leaf (with the lanolin wall) were placed into vials containing 5ml~ ,of water'containing sodium carbonate slightly in excess of saturation. The VialS wer-e 'heated to a ppro xlm at ely 99°C. , placed in a freezer at 18°C. for 24 hours, and then crushed with a stirring rod. After grinding or crushing#. each sample was centrifuged and the supernatant liquid removed: for analysis. Counting was done in a Packard tri-carb automattc scintillation counter using a solvent system consisting of 70% redistilled toluene and 30% absolute ethanol, and which contained 4.0 grams of 2..5-diphenyloxazole and O. 1 gram of 1, 4-bis-2-(5-phen,yloxazolyt)-benzene per liter. One-half ml, of supernatant liquid from a sample preparat~ was added to 191/2 nil. ---

33. 33. of scintillation solution, dispersed by shaking, and counted at 5°C. for 30 minutes (or to a count of 100,000 if this was reached first). C 14 standard solutions and scintillation blanks were used, and the counting efficiency (which was determined for each counting run) varied from 54% to 57%. . . Although other workers have reported that dalapon is easily leached from plant tissue, the sample preparation procedure was checked to determine whether or not a disproportionate amount of dalapon-2-€14 remained in the solid portion. Samples were ground, dispersed in 10 mI, of water and centrifuged. An 8 ml, aliquot was removed, 8 ml, of water were then added, and the solids redistributed by shaking. This was centrifuged and another 8 rot aliquot removed. This was done a total of four times. The va rtous aliquots were examined by liquid scintillation counting. By successive extractions, it was determined that the dalapon-2-C 14 vias readily equilibrated in the system. RES ULTS AND DISCUSSION Results obtained using different dalapon-2-C 14 and wetting agent combinations in the leaf immersion uptake test are shown in Table 1. Table 1. The Uptake of Dalapon-W ettfng Agent Solutions By the Third Leaf of Five-Leaf Quackgrass Plants Through Leaf Immersion - - - - - - - - - -%-V"ettlng Agent - uptake In - -UPtaiein - E"vi"pO"ratlOn Formulation in Solution 24 hrs. 48 hrs. in 72 hrs , ------------------------------------ Dalapon alone 0.0 O. 11 ml, 0.23 ml. 0.11 ml, Dalapon plus P-26-2 0.05 0.31 0.67 0.12 0.1 0.58 >2.0 0.09 0.2 0.98 >2.0 0.10 Dalapon plus Tergitol 0.05 0.44 0.71 0.11 TMN 0.1 0.49 >2.0 0.13 0.2 0.83 >2.0 0.11 - - - - - - - - - - - - --- - - - - - - - - ......- - - - ---- -.. "- -" .......­

.32.<br />

for plant height, weight, and rhizome weights. Six replicates were used<br />

­<br />

for each tr eatm ent,<br />

Test solutions were prepared by dispersing the wetting agent in<br />

water, and diluting to the required concentration" then adding unlabelled<br />

sodium dalapon to a concentration equivalent to 10 pounds to 60 gallons.<br />

A sample of 2_C 14 labelled sodium salt of dalapon having a specific<br />

activity of O.98 millicuries per millimole was used for the test. The<br />

oolution employed contained 1.35 mtcrocurtes per milliliter.<br />

An area 5 mm, by 50 rnrn, on the upper surface of the third leaf of<br />

each test plant was walled with lanolin. This area was then supported in a<br />

horizontal position, and flooded with one-half millilU'er of the proper<br />

dalapon-wetting agent solution. A two hundred lambda aliquot of the 2-C 14<br />

labelled sodium dalapon solution was added to the wetting agent solution on<br />

leach leaf, after which the leaves were allowed to dry.<br />

It was thought that perhaps the herbicide might be retained by the<br />

lanolin ring" or that the wetting agents might affect such a retention. This<br />

was checked in the following manner. Lanolin rings were formed on thin<br />

glass cover slips, and the rings were then filled withdalapon-2-C 14 solutions<br />

in water and with various wetting agents. After standing for one hour,<br />

the cover slips were washed under running water for ,30 seconds. The<br />

cover slips were then broken with tweezers and dropped into vials of scin­ ­<br />

tillation solvent. After shaking to dissolve the lanolin, the vials were<br />

counted and background counts were ~btained..Jt..w.as considered that the<br />

lanolin ring per se had no interaction with either the herbicide or the wetting<br />

agents used.<br />

After five days, the plants were dissected and the individual leaves,<br />

stem, rhizomes, and roots were cut with shears into one-half inch s egrn entc,<br />

The various parts, 'except 'for the treated leaves, ,,;iere ground in a glass<br />

homogeniz er-, The pieces of treated leaf (with the lanolin wall) were placed<br />

into vials containing 5ml~ ,of water'containing sodium carbonate slightly in<br />

excess of saturation. The VialS wer-e 'heated to a ppro xlm at ely 99°C. ,<br />

placed in a freezer at 18°C. for 24 hours, and then crushed with a stirring<br />

rod. After grinding or crushing#. each sample was centrifuged and the<br />

supernatant liquid removed: for analysis.<br />

Counting was done in a Packard tri-carb automattc scintillation<br />

counter using a solvent system consisting of 70% redistilled toluene and 30%<br />

absolute ethanol, and which contained 4.0 grams of 2..5-diphenyloxazole<br />

and O. 1 gram of 1, 4-bis-2-(5-phen,yloxazolyt)-benzene per liter. One-half<br />

ml, of supernatant liquid from a sample preparat~ was added to 191/2 nil.<br />

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