In observing the growth phases of a plant’s many structures, a paraphrasing of J.L. Harper (7), and later Sussman and Douthit (13), comes to mind: “Some structures are born dormant, some achieve dormancy, and some have dormancy thrust upon them”. Indeed, the dormancy phenomena can be associated with essentially all meristematic regions of the plant. Accordingly, a wealth of terminology has arisen to describe various plant dormancy phenomena. While recently discussing seasonal growth processes, our use and misuse of current and historic dormancy terms led us to conclude that a simplified, descriptive dormancy terminology would be of benefit to the plant science community. Our purpose here is to review briefly the terminology now in use, critically examine dormancy phenomena and reduce terminology to a minimal number of descriptive terms, and consequently to stimulate discussion of this terminology scheme by our peers.
Experiments were designed to alter the carbohydrate status of olive (Olea europaea L.) leaves during the presumed flower induction period. Bearing and nonbearing ‘Oblonga’ olive trees were exposed to either 850 μmol s-1n-2 PAR for 14 hr daily in a 1000 ppm CO2-enriched atmosphere, 150 μmol s-1m-2 PAR for 14 hr daily in 340 ppm CO2, or maintained in a lathhouse at ambient winter conditions of about 350 μmol s-1m-2 PAR and daily temperature fluctuations from 5° to 20°C. The trees exposed to 850 μmol s-1m-2 had 3 to 5 times the starch concentrations of either the 150 μmol s-1m-2 PAR or lathhouse treatments. There were few and inconsistent differences in sucrose, fructose or mannitol concentrations between treatments. The high levels of starch in the 850 μmol s-1m-2 PAR treatment had no effect on the flowering pattern of bearing or nonbearing trees. Gross levels of carbohydrates do not appear to limit flower induction of olive.
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