2019
DOI: 10.1007/s11627-019-10031-5
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In vitro culture and micropropagation of the Baetic-Moroccan endemic plant Lapiedra martinezii Lag. (Amaryllidaceae)

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Cited by 12 publications
(19 citation statements)
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“…Callus induction was satisfactory using several plant growth regulators. However, none of the callus produced was able to be regenerated into new plants [63].…”
Section: Horticultural Traitsmentioning
confidence: 99%
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“…Callus induction was satisfactory using several plant growth regulators. However, none of the callus produced was able to be regenerated into new plants [63].…”
Section: Horticultural Traitsmentioning
confidence: 99%
“…As a result of the quick seedling establishment, bulbils rapidly appear from young plantlets thus constituting a suitable material for in vitro initiation, swelling and ex vitro acclimatization [84]. In vitro propagation from adult bulbs was also achieved and a yield of approximately 6 bulbils per explant were obtained using solid cultures supplemented with plant growth regulators after 8 weeks of cultivation [63]. In addition, increasing the sucrose concentration up to 90 g/L in the culture medium almost doubled the biomass of bulbils produced in vitro [63].…”
Section: Horticultural Traitsmentioning
confidence: 99%
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“…Una alternativa es la micropropagación, técnica que ha sido probada exitosamente en la propagación masiva de varias especies vegetales que presentan limitaciones importantes (Anis & Ahmad, 2016;Cardoso, Sheng Gerald, & Teixeira da Silva, 2018). En especies de la familia Amaryllidaceae, el uso de esta estrategia se encuentra ampliamente documentado (El Tahchy et al, 2011;Juan-Vicedo, Pavlov, Ríos, & Casas, 2019;Rahimi Khonakdari, Rezadoost, Heydari, & Mirjalili, 2020;Zayed, El-Shamy, Berkov, Bastida, & Codina, 2011), aunque en lirio amazónico los reportes son escasos y se han centrado en el estudio de algunos factores que intervienen durante la regeneración de brotes adventicios, como el tamaño y la orientación de los explantes (escamas dobles y pedicelos), la concentración de las sales inorgánicas del medio de cultivo, la temperatura y el fotoperiodo (Hasegawa, Takigawa, & Tokuzumi, 1995;Pierik, Sprenkels, & van Bragt, 1983), así como también aquellos que participan durante la embriogénesis somática (Mujib, Banerjee, & Ghosh, 2005;Mujib, Banerjee, Maqsood, & Ghosth, 2013). El objetivo de esta investigación fue elaborar una metodología que permita la micropropagación de esta especie mediante organogénesis directa con el fin de incrementar las tasas de propagación y obtener material homogéneo.…”
Section: Introductionunclassified