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second temperature for approximately 8 hours per day. The temperature shall be determined at the substratum level and shall be as uniform as possible throughout the germination chamber. (A sharp alternation of temperature, such as obtained by hand transfer, may be beneficial in breaking dormancy.) If tests are not subjected to alternating temperatures over weekends and on holidays, they are to be held at the firstmentioned temperature during this time. In cases where two temperatures are indicated (separated by a semicolon) the first temperature shall be regarded as the regular method and the second as an alternate method.

(9) Paper substrata must be free of chemicals toxic to germinating seed and seedling growth. If root injury occurs from toxicity of a paper substratum or from the use of potassium nitrate, retests shall be made on soil or on a substratum moistened with water.

(b) Special procedures and alternate methods for germination referred to in table 2-(1) Alyce clover (Alysicarpus vaginalis); Swollen seeds. At the conclusion of the 21-day test period carefully pierce the seedcoat with a sharp instrument and continue the test for 5 additional days.

Alternate method: The swollen seeds may be placed at 20° C. for 48 hours and then at 35° C. for 3 additional days.

(2) Bahia grass (Paspalum notatum); removal of glumes—(i) Vars. Common and Argentine. Remove the glumes with the aid of a sharp scalpel. If the seed is fresh or dormant scratch the surface of the caryopsis lightly and use potassium nitrate.

(ii) Var. Pensacola. The glumes shall not be removed for the germination test.

(3) Beet, Swiss chard (Beta); preparation of seed for test. Before placing the seeds on the germination substratum they shall be soaked in water for 2 hours, using at least 250 ml. of water per 100 seeds, then washed in running water and the excess water should be blotted off. The temperature of the soaking and washing water should be no lower than 20° C. Samples producing darkened radicles should be retested in soil or by washing in running water for 3 hours and tested on "Kimpak," keeping the seed covered with slightly moist blotters.

(4) Buffelgrass (Pennisetum ciliare); alternate method for dormant seed. The caryopses shall be removed from the

fascicles and placed on blotters moistened with a 0.2 percent potassium nitrate solution, in Petri dishes. The seeds from a fascicle should be arranged so they will not be confused with seeds from other fascicles during the test. The seeds are then prechilled at 5° C. for 7 days and tested at 30° C. in light for 21 additional days. Firm ungerminated seeds remaining at the conclusion of the test should be scratched lightly and left in test for 7 additional days.

(5) Cotton (Gossypium spp.); dormant samples. Samples of cottonseed which do not respond to the usual method should be placed in a closed container with water and shaken until the lint is thoroughly wet. The excess moisture should then be blotted off.

(6) Endive (Cichorium endivia); dormant samples. Add about 1⁄2 inch of tap water at the beginning of the test and remove excess water after 24 hours.

(7) Lettuce (Lactuca sativa); light exposure. All samples should be given at least 2 hour of light after being placed on the moist substratum. Additional light during the test period is desirable for dormant samples and facilitates seedling interpretation for samples of low vigor.

(8) Rescue grass (Bromus catharticus); dormant samples. Wash for 48 hours in running water, or soak for 48 hours, changing the water and rinsing each morning and night.

(9) Rice (Oryza sativa)—Alternate method: Plant the seeds in moist sand. On the seventh day of the test add water to a depth of one-fourth inch above the sand level and leave for the remainder of the test. Only a final count is made. Dormant seeds: Presoak 24 to 48 hours in 40° C. water. For deeply dormant seeds, presoak 24 hours in 1,000 p.p.m. ethylene chlorohydrin or 5 percent solution of sodium hypochlorite (clorox at bottle strength).

(10) Ryegrass (Lolium); fluorescence test. The germination test for the fluorescence of ryegrass shall be conducted in light (not to exceed 100 foot-candles) with white filter paper as a substratum. The test shall be conducted in a manner that will prevent the contact of roots of different seedlings.

(11) Trifolium, Medicago, Melilotus, and Vicia faba; temperature requirements. A temperature of 18° C. is desirable for Trifolium spp., Medicago spp., Melilotus spp., and Vicia faba.

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(c) Table 2; germination requirements for indicated kinds.

TABLE 2-GERMINATION REQUIREMENTS FOR INDICATED KINDS

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See footnotes at end of table.

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TABLE 2-GERMINATION REQUIREMENTS FOR INDICATED KINDS-Continued

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Photos 2407, 2408, 2524-2527, 19545, 19546.

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Remove shells; photos 19541, 19542.

18 Photos 2503, 2506, 14543-14547.

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28 Light; see par. (b) (8) for alternate Light; KNO3

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14 Photos 19549, 19550; see par. (b) (9) Presoak, see par. (b) (9). for alternate method.

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7 Photos 2403, 2406, 2528-2531.

Prechill at 5° C. for 4 weeks and test for 21 additional days.

Prechill st 5° or 10° C. for 5 days or predry.

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See footnotes at end of table.

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