Abstract

Abstract Rumohra adiantiformis, also known as “leatherleaf fern”, is an ornamental species that, because of its long display life, is widely used in floral arrangements. In this study, a new protocol for in vitro regeneration of the leatherleaf fern was established. For spore germination, two culture media (MS and Knop) were assessed with presence or absence of 1g L−1 activated charcoal (AC) under different light and dark conditions. Frond, frond microcuttings, and prothallus explants were evaluated on Knop regeneration medium supplemented with 1g L−1 AC, 0.5% agar, pH 5.0 in combination with 2,4 dichlorophenoxyacetic acid (2,4-D: 0.0, 0.1, 0.5 and 1.0 mg L−1) and 6-benzylamino purine (BA: 0.0, 0.1, 0.5 and 1.0 mg L−1). For rooting, four levels of α-naphthaleneacetic acid (NAA: 0.0, 0.01, 0.1 and 0.2 mg L−1) were tested. After 18 days of culture, spore germination rate was 100% on Knop medium with AC and 8 h light/16 h dark. After 120 days of culture, sporophytes 1.7 ± 0.4 cm in length developed on Knop m...

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