Claim · model-written summary
Lily bulblets cultured at 20 or 25°C for 11 weeks were dormant and needed cold for rapid emergence.
Not reportedMaterialGeneCompoundOrgan / stageInteractorInteractor roleSecond interactorSecond interactor roleTreatmentComparatorSettingDirectionValue
Organisms pictured · Representative pictures of the matched species, not figures from the paper.

Verbatim
e0“Lily plantlets regenerated in vitro on scale explants at 20 or 25°C were harvested after 11 weeks, and the leaves were removed from the bulblets. The bulblets were dormant and required a cold treatment to achieve rapid emergence after planting in soil”
Title
Kwang‐Soo Kim; Evert Davelaar; Geert‐Jan De Klerk Physiologia Plantarum 1994. doi:10.1111/j.1399-3054.1994.tb02192.x
Other claims from this paper (12)
- Intervention effect Fluridone inhibited lily petiole swelling and promoted leaf formation.
- Intervention effect High fluridone concentrations completely blocked lily petiole swelling.
- Intervention effect High fluridone concentrations produced lily plantlets with leaves only.
- Intervention effect ABA addition produced lily plantlets with scales only.
- Intervention effect Simultaneous ABA nullified the fluridone effect on lily plantlet organ formation.
- Intervention effect Fluridone prevented lily bulblet dormancy during in vitro culture.
- Intervention effect Fluridone-treated lily bulblets did not require cold treatment.
- Intervention effect Simultaneous ABA nullified the fluridone effect on lily bulblet dormancy.
- Observation Lily bulblets harvested after six weeks at 20°C had not developed dormancy.
- Observation Lily bulblets regenerated at 15°C were only slightly dormant.
- Intervention effect ABA addition did not affect dormancy of the six-week or 15°C lily bulblets.
- Mechanism Endogenous ABA and an unknown additional factor play major roles in lily dormancy development.