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, so forming an extensive surface of medium extending from the bottom of the tube almost to its mouth. This is employed for "streak" or "smear" cultivations (_Strichcultur_). 2. Straight tube (Fig. 119), in which the medium forms a cylindrical mass in the lower portion of the tube and presents an upper surface which is at right angles to the long axis of the tube. This is employed for "stab" or "stick" cultivations (_Stichcultur_), or by inoculating the medium whilst fluid, and allowing to solidify in this position, for "shake" cultivations. _Streak Culture._-- 1. Flame the plugs, sterilise the platinum loop (or spatula). Open the tubes and charge the loop as in previous inoculation. 2. Pass the infected loop to the bottom of the tube to be inoculated and draw it, as lightly as possible, along the centre of the surface of the medium, terminating the "streak" over the thin layer of medium near the mouth of the tube. 3. Replug the tubes, sterilise the platinum loop. 4. Label the newly inoculated tube and incubate. _Smear Culture._--Proceed generally as in streak culture, but rub the infected loop all over the surface of the medium, instead of restricting the inoculation to a narrow line. NOTE.--Gelatine and agar oblique tubes should be freshly "slanted" before use. _Stab Culture._-- 1. Flame the plugs, open the tubes, sterilise the platinum needle and charge it with the inoculum as in the previous cultivations. 2. Pass the platinum needle into the tube to be inoculated until it touches the centre of the surface of the medium. Now thrust it deeply into the substance of the medium, keeping the needle as nearly as possible in the axis of the cylinder of medium. Then withdraw the needle. 3. Replug the tubes. Sterilise the platinum needle. 4. Label the newly planted tube and incubate. NOTE.--When gelatine is stored for some time the upper surface of the cylinder becomes concave owing to evaporation. Tubes showing this appearance should be liquefied and again allowed to set before use for stab culture, otherwise when the needle enters the medium, the surface tension will cause the gelatine cylinder to split. [Illustration: FIG. 118.--Sloped or slanted medium for streak or smear culture.] [Illustration: FIG. 119.--Straight tube.] _Shake Culture._-- 1. Liquefy a tube of nutrient gelatine (or agar, or other similar medium), by heating in a w
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