Abstract
Blackberry micropropagation (Rubus spp.) and effects of substrates in plants acclimatization. The objective of the present study was to achieve the improved techniques in in vitro propagation and to determine a better substrate for the blackberry. The first experiment consisted of nodal segments of plants with ±2 cm of length obtained from in vitro culture cv. Ebano, excised and inoculated in MS culture medium, supplemented with five activated charcoal concentrations and five BAP concentrations. Both experiments were entirely performed in a design randomized complete block, using in vitro 3 explants by repetition and 4 replications for treatment and in greenhouse, a factorial 4x4. The pH of the culture medium was adjusted to 5.8 before the addition of 6 g L -1 of agar and the sterilization to 121oC and 1 atm for 20 minutes. After 70 days, several parameters in the explants were evaluated. A greater number of leaves and roots were obtained with 0.5 mg L -1 of BAP. The number of roots and their length were larger in the presence of 3 g L -1 of activated charcoal. A larger weight of the fresh matter was obtained in the absence of activated charcoal. The second experiment consisted of plants cv. Cherokee maintained in in vitro conditions and transplanted to plastic trays, containing the substrates and kept in greenhouse. Four types of substrates were tested. After 100 days of acclimatization, the leaf number, root length and aerial part, cool and dry root weight and cool and dry aerial part weight had been evaluated. It was concluded that the acclimatization can be successfully performed using Plantmax followed by the Plantmax + vermiculita + rind rice carbonized mixture. There was a 92% rate of the plants' survival in all substrates.
Highlights
Os maiores produtores de amora-preta na América do Sul são a Argentina e o Chile (Jennings e McNicol, 1991)
Atualmente, além da propagação tradicional, a micropropagação da amoreira-preta é considerada uma outra alternativa viável, com o intuito de se obter plantas livres de vírus, geneticamente uniformes e em curto espaço de tempo (Antunes, 1999)
‘Cherokee’ mantidas em condições in vitro, em tubos de ensaio, contendo meio de cultura MS acrescido de 1,0 mg L-1 de BAP e mantidas em sala de crescimento com 27±1oC, irradiância de 35 μ mol m–2.s–1 e fotoperíodo de 16 horas diárias durante 60 dias
Summary
O experimento foi instalado e conduzido na Universidade Federal de Lavras, Departamento de Agricultura, Lavras, Estado de Minas Gerais, no Laboratório de Cultura de Tecidos Vegetais e em casade-vegetação com aproximadamente 90% de umidade do ar, temperatura controlada e nebulização intermitente. Os explantes foram inoculados em tubo de ensaio contendo 15 mL de meio constituído dos sais minerais do meio MS (Murashige e Skoog, 1962), combinados com 5 concentrações de BAP (0; 0,5; 1,0; 2,0 e 4,0 mg L-1) e 5 de carvão ativado (0; 1,0; 2,0; 3,0 e 4,0 g L-1). Posteriormente foram transferidos para sala de crescimento a 27±1oC, irradiância de 35 μ mol m–2 s–1 e fotoperíodo de 16 horas, permanecendo nessas condições por 70 dias. ‘Cherokee’ mantidas em condições in vitro, em tubos de ensaio, contendo meio de cultura MS acrescido de 1,0 mg L-1 de BAP e mantidas em sala de crescimento com 27±1oC, irradiância de 35 μ mol m–2.s–1 e fotoperíodo de 16 horas diárias durante 60 dias. Após 100 dias de aclimatização, foram avaliados os parâmetros número de folhas, comprimento das raízes e da parte aérea, peso fresco e seco das raízes e peso fresco e seco da parte aérea
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