Abstract
Abstract. The duration of the G1 period in meristematic cells has been measured directly at two different temperatures by using a synchronous cell population ‘labelled’ as binucleate by treatment with caffeine. By studying the uptake of a radioactive DNA‐precursor, it proved possible to determine the duration of the G1 period in relation to the total interphase duration, at two temperatures tested, and to demonstrate that the relationship remained constant.
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