2013
DOI: 10.1590/s1984-70332013000400002
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Cytological characterization of Jatropha curcas callus in different periods of cultivation

Abstract: -The aimed was characterization and determining the time for

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Cited by 4 publications
(5 citation statements)
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“…In the present study, starch grains could be observed until the 28 th day of culture, after which cell masses lose their embryogenic characteristics ( Figure 4F and H). Embryogenic structures do not continue their development during the stationary phase because cells go into decline and lose their intracellular organization due to the process of senescence (Santos et al, 2013). Therefore, transfer to a new culture medium can maintain the continuity of development, resulting in a greater proliferation of cells with embryogenic potential.…”
Section: Discussionmentioning
confidence: 99%
“…In the present study, starch grains could be observed until the 28 th day of culture, after which cell masses lose their embryogenic characteristics ( Figure 4F and H). Embryogenic structures do not continue their development during the stationary phase because cells go into decline and lose their intracellular organization due to the process of senescence (Santos et al, 2013). Therefore, transfer to a new culture medium can maintain the continuity of development, resulting in a greater proliferation of cells with embryogenic potential.…”
Section: Discussionmentioning
confidence: 99%
“…In the linear phase, few cells were capable of multiplication, and the observed decrease in the mitotic index is indicative that the cells are prepared for cell differentiation (Santos et al 2013). However, in this period, cell growth and development are more evident (Landa et al 2000), because the cells grow in volume (Feitosa et al 2013).…”
Section: Discussionmentioning
confidence: 99%
“…These pigments may be related to senescence of callus, due to stress caused by the possible shortage of nutrients, water and/or growth regulators, resulting in an increase of free radicals, toxic to the plant (Valle 2003). The low cell viability and mitotic index are because cells are not able to divide, become senescent and die (Santos et al 2013).…”
Section: Discussionmentioning
confidence: 99%
“…Calos advindos de um dos cotilédones, cultivados em meio MS, suplementado com 0,5 mg L -1 de 2,4-D + 2,0 mg L -1 de picloram + 0,5 mg L -1 de cinetina + 2,0 mg L -1 de BAP, foram repicados duas vezes, em intervalos de 30 dias. Após a segunda repicagem, foi estabelecida a curva de crescimento dos calos por meio da determinação da massa fresca a partir do dia da inoculação (tempo 0), em intervalos de sete dias, durante 112 dias (Santos et al, 2013).…”
Section: Metodologiaunclassified