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The maturation and phase change processes in woody species have not been completely clarified, specially the role of growth regulators during the maturation phase. Understanding their role better will allow to comprehend the physiological aspects of the species, which would allow to chose the optimal management conditions in forestry programs and make them more useful. In the present study, the endogenous content of abscisic acid (ABA) and 3-indolacetic acid (IAA) were quantified by high performance liquid chromatography, in the reinvigoration process of elite Pinus radiata material, during the development of homomicrografts (P. radiata/P. radiata) and heteromicrografts (P. radiata/Pinus caribaea), developed under in vitro conditions. The results showed an increase in the endogenous content of ABA through time and a decrease in the content of IAA. Significant differences were found in the endogenous content of ABA, where the maximum values were detected at 120 days of micrograft culture, being similar to the values obtained in juvenile buds. As well, significant differences were also detected in the endogenous content of IAA in the micrografted buds during all the development phases, compared with adult buds. However, no significant differences were detected in the endogenous content of ABA and IAA, regarding the type of rootstock employed. Considering the endogenous content of ABA and IAA, the micrografted plant material would be equal to the juvenile buds, since statistically they were equal to these buds, considering that the values obtained in this case are independent from the type of rootstock used.

Rhodophiala C. Presl (Amaryllidaceae) is a genus of attractive flowering geophytes native to South America. They have ornamental value, but most species are not well-known and have conservation problems. The objective of this study was to optimize a micropropagation process to support the use and preservation of three Chilean native species, R. montana (Phil.) Traub, R. splendens (Rengifo) Traub., and R. ananuca (Phil.) Traub. The research evaluated the feasibility of implementing liquid medium culture and assessed the influence of different tissue culture systems on the shoot production and biomass increment of small bulbs. Three experiments were carried out. The first one determined the influences of flask size and volume of media; the second compared liquid and solid media, and in the third experiment, a temporary immersion system (TIS), and conventional culture in static liquid, shaken liquid and gelled Murashige and Skoog (MS) media were compared. By using larger (350 mL) flasks with higher (50 mL) media volume, 100% more fresh weight of microbulb was obtained that treatment with smaller flasks (45 mL) and media volume (10 mL). In gelled medium, hyperhydricity affected only 5% of explants, while in liquid medium was 16-40%. Survival to acclimatization reached 87-94% for plants from gelled medium; from liquid medium only 38-69%. TIS yielded higher propagation rate (1.9 shoots in 30 d) compared with shaken liquid medium (1.0) (P < 0.05) in R. ananuca only. Current procedures are appropriate for the support of ex situ conservation and germplasm bank establishment.

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