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Factors affecting the induction and release of secondary dormancy in Kalanchoë seeds
Author(s) -
RETHY R.,
DEDONDER A.,
FREDERICQ H.,
GREEF J.
Publication year - 1983
Publication title -
plant, cell and environment
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.646
H-Index - 200
eISSN - 1365-3040
pISSN - 0140-7791
DOI - 10.1111/1365-3040.ep11589352
Subject(s) - dormancy , germination , incubation , biology , seed dormancy , horticulture , botany , gibberellin , biochemistry
Abstract. Several short daily R irradiations are required from the first day of incubation on water to induce germination of Kalanchoë seeds. When the same light treatment is given after a prolonged dark incubation period at 20°C, secondary dormancy prevents germination. Factors controlling the induction and breaking of secondary dormancy have been investigated. The induction of secondary dormancy is very temperature dependent. Locally puncturing the seed coat strongly delays it. Secondary dormancy is not induced in the presence of GA 3 during the first 10 d of dark incubation, although this growth substance cannot induce dark germination. Prolonged or cyclic daily R irradiations can relieve secondary dormancy of seeds kept on water, even after a dark period of 20 d. A 24 h treatment at 4°C restores responsiveness to short R exposures of slightly secondarily dormant seeds. The synergism between GA 3 and Pfr in non‐dormant Kalanchoë seeds, leading to high effectiveness of even one short FR irradiation, still occurs in seeds made secondarily dormant before transfer to GA 3 , but more R or FR irradiations, in combination with GA 3 , are required for the release of secondary dormancy. A combination of red light and 6‐benzyl‐aminopurine is ineffective in removing dormancy.