Citronella mucronata (C. mucronata), a tree species endemic to Chile, has become threatened in its natural habitat and is currently listed as vulnerable. Tree population parameters have deteriorated due to indiscriminate logging and other anthropogenic activities, warranting research on mass propagation as a means of recovery. This study, unprecedented for this native species, has developed a successful method for its micropropagation. The objective was to establish a protocol for in vitro propagation of C. mucronata to produce large quantities of high-quality seedlings in an accelerated plant acquisition process. The best results were achieved by growing explants on Murashige and Skoog (MS) basal culture medium supplemented with 4.44 μM 6-benzylaminopurine (BAP) and 14.76 μM indole-3-butyric acid (IBA). Explant survival rate was 78 %, the average shoot length reached 3.2 cm, the number of lateral shoots was 3.9, and rooting rate was 60%. Furthermore, stimulation with red and blue light in a 1:2 ratio, supplemented with 14.76 μM IBA, improved the rooting rate to 93%. The survival rate of rooted explants reached 100% in the acclimatization stage when using peat and perlite substrate (1:1 v/v).
Alstroemeria pelegrina (A. pelegrina), a Chilean endemic, is considered vulnerable as its natural habitat is currently threatened. The decline in the reproductive capacity of the species due to anthropogenic impacts and climate change has made it imperative to address the problem by developing large-scale propagation methods. The objective of this study was to establish protocols for breaking the dormancy and in vitro germination of A. pelegrina seeds to speed up the germination and seedling production processes. The research began with morphological observations of the reproductive process, followed by in vitro sowing. The results showed that the seeds reached full maturity in 51 days, and physiological maturity in 41 days, at which point the seeds could be harvested for in vitro germination. The mechanical scarification pretreatment improves the in vitro germination rate to 96% and the germination time to 7 days, showing that the species is characterized by physical seed dormancy. On the other hand, if the seed coat incisions are deeper than 0.5 mm, 30% of the potential plants are lost due to embryo damage. The study provides scientific evidence for the feasibility of large-scale in vitro propagation of the species and establishes an efficient method of seedling production.
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