Vol. 15â1961 - NorthEastern Weed Science Society
Vol. 15â1961 - NorthEastern Weed Science Society Vol. 15â1961 - NorthEastern Weed Science Society
346 • .Absornt:j.Qn Qn Exchange Resins I To determine if e. charge exists on the inhibitor ~oleoule, water extraot was leached through coltmms of both amberlite cation exch~nge resin (m-120) and amberlite anion exchange resin fmA-4QO). The ... filtrate ,;as testEd fo.r retention Qf inhibitory activity with the results given in Table 11. . Table 11. Gemination and Root Gro"lth Following Passage of Extractions through Exchange Resins Treatment tlGermUlition Radiole length (mm) Anion Exchange Resin Filtrate Cation Bxchange Resin Filtrate Both Resins 10 5 Water Extract Control (\'-Jater) 90 o o o There 'WaS no loss of inhibitory activity after leaching through the resin. Absorpt:j.on Qf Activ:ated CharCOal' A test using 25 m1. of wat.er extract and 2 gra."llS of activated charcoal (Norit A, netural, deco10rbing charcoal) was shaken together for 20'minutes on a wrist action mechanical shaker, and filtered on a Buckner funnel. A test of the activity of the filtrate gave the res~ts in Tab1e'12 • . Table 12. The Effect of Activated Carbon on the !nhibitor Trea;t.men1( %Germination RAdicle l;enrlh (mm) Norit - A Water Extract o - Control (Water) 100 2S o , . The assa;y indicated that no absorption of the. inhibitor by the activated carbor. • .occurred. Chromatogranhy: Paper 98rtiti6n chrcmabography techniques were used to further characterize the inhibitor (s}, ~1ethanol extractions of the foxtail were . concentrated byheatdng and then deco1orizing. The solvent was prepared from n-butyl alcohol, acetic acid, and "later, 4-1-5 ratio,by volume. Thismixture was separated in a senaratory funnel and 'only the organic layer used as the solvent. The descending method of ohromatography \'65 employed. A pencil line was drawn across a strip of \fhatman! s filter ryaper, three inches from .the end. The paper was 20 x 7 inches. The concentrated methanol
extraction was applied along the pencil line "lith a pipette drawn to a fine point. Five applications were made tvith a period of drying between each. The end of the paper nearest the pencil line was then inserted in a trough of the solvent. The i'llhole was then suspended in a glass chamber. A petri dish of the solvent was placed in the bottom of the chamber to maintain a saturated atmosphere.' When the solvent front had advanced a suitable distance along the paper strip, the paper was removed and, dried in a hood. The chromatograms .were cut in'1.5 inch strips at right angles to the movement of the solvents. For assay, sections from each strip along with 10 alfalfa seeds and 1 ml., of "rater were placed in crucible lids and covered with watch glasses. The diameter of the crucible lid was 1.25 inches. Twocontrols were run "lith each assay, a Water control and one from the chromatogram that only the solvent had covered. 'Table l3'indicates the data from the assays. The solvent'front had moved 15.5 inches. Tne numbers each represent consecutive strips of 1. 5 inches from the starting spot. .. 347. Table 13. Bioassay of Chromatogramed Extract Chromatogram Section %Germina:tion Radicle lengjih from) Check - water 90 17 Check - solvent 95 10 1 90 7 2 0 0 3' 90 6 4 100 6 5 70 11 6 100 10 7 60 3 B 90 9 9 100 14 10 60 s Areas'2 and 7 reryresent regions of strong inhibition tvith Rf values of 0;13 and 0;75. Areas 5 and 10 exhibited slight inhibition ,'lith Rf' values of 0.40 and 0.90. A section of the chromatogram was develoned for a general sugar test. The test consisted of: a. Silver nitrate saturated water 0.1 vol., . Acetone . 20 vol. b. Sodium hyrlroxide, 0.5% in ethanol
- Page 295 and 296: • •• ., .. • •• ',' •
- Page 297 and 298: 297. compatible with grub-proofing
- Page 299 and 300: 299, Diphenatrile Results During th
- Page 301 and 302: 301. tentative generic name triflur
- Page 303 and 304: - 1 PRE-ENERGENCE CRABGRASS CONTROL
- Page 305 and 306: Discussion 30; • a) Pre-emergence
- Page 307 and 308: 307. TABLEI -- Comparison of Produc
- Page 309 and 310: -' Table II (can't) 309. Stand of S
- Page 312 and 313: 312. THEEFFECTIVENESSOF COMBINATION
- Page 314 and 315: 314. Table 2. Stand Counts and Sile
- Page 316 and 317: 316. planted control before these h
- Page 318 and 319: Table II. The control of quackgrass
- Page 320 and 321: 320. growing season in the 1957-59
- Page 322 and 323: 322. Table I Main Effects of Cultur
- Page 324 and 325: 324. Atrazine by September 10 when
- Page 326 and 327: 326. Another effect of Atrazine tha
- Page 328 and 329: 32S. Amitrol-T was intermediate in
- Page 330 and 331: Qolumn Separation: Cellulose. A 24
- Page 332 and 333: 332, Figure -I. Chromatogram of qua
- Page 334 and 335: 334. PRELIMINARYRESULTSONTHE USE OF
- Page 336 and 337: 336. DATEOF BERRYHARVESTAS IT AFFEC
- Page 338 and 339: within three inches of the soIl sur
- Page 340 and 341: 340 .. The growth ra.te of Horse ne
- Page 342 and 343: 342. dish containing ten seeds bet\
- Page 344 and 345: 344. is not a factor in in It is
- Page 348 and 349: 348. The' chrona tog ram."WaS first
- Page 350 and 351: 350. PROGRESSREPORTON A STUDYOF THE
- Page 352 and 353: 352. 7. Fluctuating warm and cold w
- Page 354 and 355: 354. A clos.e correlation was found
- Page 356 and 357: 356. 1 THE ANATOMICAL NATUREO:BTHE
- Page 358 and 359: 358. The 2,4,5-TP was most effectiv
- Page 360 and 361: Table I. Effect. of Pre-emergence T
- Page 362 and 363: INTRODUCIIOB: THEEFFECTOF WEEDCOMPE
- Page 364 and 365: 1";. 1958 JFab1e I (cont ' d) Treat
- Page 366 and 367: 366. fiE USE OF FENACFOR QUACKGRASS
- Page 368 and 369: 36$. SUMMARY: Based on a I).umber o
- Page 370 and 371: - Table 1. Chemicals and Rates Used
- Page 372 and 373: 372. On spring plowed plots I where
- Page 374 and 375: Table 1. Treat.ments Used and Stand
- Page 376 and 377: 37t. PRELIMINARYRESULTSONTHE CONTRO
- Page 378 and 379: 378. CHEMICAL TREATMENTS FORTHECONT
- Page 380 and 381: Table ;. Visual RatiDgs and Stand C
- Page 382 and 383: ANN11AL WEEDCONTROL IN SILAGECORN1
- Page 384 and 385: TABLEI. field Corn tiead Control an
- Page 386 and 387: Sunderiand,' Mass..Experiment: In t
- Page 388 and 389: ) ) BBLB I. QuackgT88S Control in F
- Page 390 and 391: TABLEIII. Quackgr888 Control in Fie
- Page 392 and 393: 392. herbicides. In senerel."we.had
- Page 394 and 395: 394. RESULTS§e PISCUSSION In Augus
346 •<br />
.Absornt:j.Qn Qn Exchange Resins I To determine if e. charge exists on the inhibitor<br />
~oleoule, water extraot was leached through coltmms of both amberlite cation<br />
exch~nge resin (m-120) and amberlite anion exchange resin fmA-4QO). The ...<br />
filtrate ,;as testEd fo.r retention Qf inhibitory activity with the results<br />
given in Table 11. .<br />
Table 11. Gemination and Root Gro"lth Following Passage of<br />
Extractions through Exchange Resins<br />
Treatment tlGermUlition Radiole length (mm)<br />
Anion Exchange Resin Filtrate<br />
Cation Bxchange Resin Filtrate<br />
Both Resins 10 5<br />
Water Extract<br />
Control (\'-Jater) 90<br />
o<br />
o<br />
o<br />
There 'WaS no loss of inhibitory activity after leaching through the resin.<br />
Absorpt:j.on Qf Activ:ated CharCOal' A test using 25 m1. of wat.er extract and 2 gra."llS<br />
of activated charcoal (Norit A, netural, deco10rbing charcoal) was shaken together<br />
for 20'minutes on a wrist action mechanical shaker, and filtered on a Buckner<br />
funnel. A test of the activity of the filtrate gave the res~ts in Tab1e'12 •<br />
. Table 12. The Effect of Activated Carbon on the !nhibitor<br />
Trea;t.men1( %Germination RAdicle l;enrlh (mm)<br />
Norit - A<br />
Water Extract o<br />
-<br />
Control (Water) 100 2S<br />
o<br />
, .<br />
The assa;y indicated that no absorption of the. inhibitor by the activated carbor. •<br />
.occurred.<br />
Chromatogranhy: Paper 98rtiti6n chrcmabography techniques were used to further<br />
characterize the inhibitor (s}, ~1ethanol extractions of the foxtail were .<br />
concentrated byheatdng and then deco1orizing. The solvent was prepared from<br />
n-butyl alcohol, acetic acid, and "later, 4-1-5 ratio,by volume. Thismixture<br />
was separated in a senaratory funnel and 'only the organic layer used as the<br />
solvent. The descending method of ohromatography \'65 employed.<br />
A pencil line was drawn across a strip of \fhatman! s filter ryaper, three<br />
inches from .the end. The paper was 20 x 7 inches. The concentrated methanol