No abstract

Continues subculturing of in vitro plant subcultures is essential for commercial micropropagation and tissue culture research. In unusual situations, the subcultures can be delayed, and the slow-growth in vitro storage technic could be applied to reduce the loss of plant material. The present study aimed to evaluate the slow-growth in vitro storage of banana plantlets (‘Prata Catarina’; group AAB) under different light spectra. Shoot cultures in MS medium without plant growth regulators were maintained under blue (B), red (R), red plus blue (R2B), and white (CW) light spectra (25 °C ± 2 °C; 50 µmol m −2 s −1 ) for up to 140 days. The plantlets maintained under the R, CW, and R2B spectra suffered severe root damage and browning after 140 days of in vitro slow-growth storage (SGS). All plantlets maintained under the B spectrum survived after 140 days of in vitro SGS and showed little browning.

Maintaining updated in vitro plant subcultures is essential for commercial micropropagation and tissue culture research. In unusual situations, the subcultures can be delay and the slow-growth in vitro storage technic could be applied to reduce the loss of plant material. The present study aimed to evaluate the slow-growth in vitro storage of banana plantlets (‘Prata Catarina’; group AAB) under different light spectra. Shoot cultures in MS medium without plant growth regulators were maintained under blue (B), red (R), red plus blue (R2B), and white (CW) light spectra (25°C ± 2°C; 50 µmol m -2 s -1 ) for up to 140 days. The plantlets maintained under the R, CW, and R2B spectra did not survive after 140 days of in vitro slow-growth storage. The plantlets maintained under the B spectrum survived after 140 days of in vitro slow-growth storage and showed little browning.

Couroupita guianensis Aubl. is an Amazonian forest species with important medicinal and ornamental value. This study evaluated the effect of different culture media and light spectra on the in vitro germination and development of the zygotic embryos of C. guianensis. The culture media, MS and WPM, were evaluated without the addition of plant growth regulators and were associated with four LED light spectra: white (CW), 70% red + 30% blue (R2B), 100% red (R), and 100% blue (B). One hundred percent of the seeds successfully underwent in vitro germination, and the culture media did not interfere with embryo development. In addition to this, the different light spectra induced in vitro morphogenesis and R2B treatment significantly promoted the production of secondary roots. This effect may aid in the rooting and acclimatization of seedlings of this species.

The time spent by urban residents indoors has been increasing annually, thus, prioritizing the enhancement of indoor spaces into green spaces to improve the quality of life. Even with limited environmental conditions indoors, an active living wall and LED light techniques have enabled us to explore indoor green environments. In the present study, the yellow/orange-colored flowers invasive ornamental species,Lantana camara‘splendens’, was cultivated in 4.0 m2 of the active living wall under a non-decorative LED lamp, adjusted to optimize performance in the coverage area. This study evaluated the development of lantana in the active living wall under different light intensities (135 watts and 90 watts) in a room with light restriction. Parameters such as plant height, flowering, SPAD chlorophyll content, and vegetative cover were analyzed. The results indicated that Lantana camara ‘splendens’ is suitable for use in active living walls and blooms at a low light intensity when the light is uniformly applied.