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Vol. 16—1962 - NorthEastern Weed Science Society

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non-polar solvents. Table 5 shows that an inhibition extracted with chloro#o~<br />

can be separated from the chloroform by shaking with water in a separatory 'funnel.<br />

Similar results were obtained with benzene.<br />

Table S. Removal of activity from chloroform with<br />

water in a separatory funnel •<br />

._-._._---_..-.-..... _.-..---------------_.-.-.--<br />

Percent<br />

geradnation<br />

Percent<br />

inhibition<br />

---_._.-._-_---.' -.- - _-----_.<br />

Extracted<br />

Chloroform<br />

Water Extract<br />

80<br />

30<br />

24<br />

70'<br />

235<br />

Whenone g. dry meal was asbed at 625OC. for 4 hours and 20 ml. water<br />

added to the ash to makeup a test solution, alfalfa seedlings grew as well: as<br />

,controls (Table 6). The ash solution was basic (pH 12.2). HN03was added"to<br />

bring the solution to pH 7. However, seedlings grew well in both solutio~s.<br />

Growth in the basic solution is explained by spcretion of organic acids from<br />

the alfalfa s4edlings as the pH in the basic test bad come down to near pH 7<br />

at the end of 4 days seedling growth.<br />

Table 6<br />

The effect of ash on inhibltion of'<br />

alfalfa seedlings.<br />

Dialysis<br />

-----------------~_!~~~~~--_:~~~~~~~~~-----<br />

Control 37 00<br />

Ash (No neutral~aatten<br />

treatment)' 42 -13<br />

Ash (Neutralized<br />

with HN0 3) 39 - 5<br />

.-.~--~._-.--.---...._._..----_..-_.<br />

__.._---<br />

Autoclaved extract was placed in cellophane dtalycer tubing and the tubing<br />

inserted in a cylinder. Water in the cylinder was changed about 10 times during<br />

three days treatment. All material outside the cylinder and the heavy concentrate<br />

which did not pass through the casing were concentrated and diluted for<br />

asaay. Table 7 shows most of the activity passed through the cellophane tubing.

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