1997
DOI: 10.1201/9781420049275.ch4
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In Vitro Conservation of Plant Genetic Resources

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Cited by 62 publications
(55 citation statements)
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“…& Alina Trejgell trejgell@umk.pl material for a few months to several years (depending on the species) under tissue culture conditions, requiring only infrequent subculturing (Rao 2004). Slow growth of in vitro cultures can be achieved by reducing the osmotic potential of the storage medium, lowering incubation temperature or altering medium composition and photon flux density (Withers and Engelmann 1997). The most important factor in the slow growth culture is temperature reduction, often with a simultaneous decrease in light intensity or even culture in the dark, which limits shoot growth from callus induction and proliferation of the base of the shoots.…”
Section: Introductionmentioning
confidence: 99%
“…& Alina Trejgell trejgell@umk.pl material for a few months to several years (depending on the species) under tissue culture conditions, requiring only infrequent subculturing (Rao 2004). Slow growth of in vitro cultures can be achieved by reducing the osmotic potential of the storage medium, lowering incubation temperature or altering medium composition and photon flux density (Withers and Engelmann 1997). The most important factor in the slow growth culture is temperature reduction, often with a simultaneous decrease in light intensity or even culture in the dark, which limits shoot growth from callus induction and proliferation of the base of the shoots.…”
Section: Introductionmentioning
confidence: 99%
“…Temperatures of 0-5ºC are used with cold tolerant species, but, temperatures of 15º-20ºC are recommended for tropical species. Growth can also be limited by modifying the culture medium, mainly by sugar reducing and changes concentration mineral elements and by covering explants with a layer of liquid medium or mineral oil for reduction of oxygen level in cultures (Withers and Engelmann 1997). According to Withers and Engelmann (1997) successful regeneration and propagation of stable seedlings from in-vitro cultures are pre-requisites for any in-vitro conservation and techniques for clonal multiplication are well established for a number of species and slow growth procedures have been developed for a wide range of species; however, they are routinely used only for a few species including banana, potato, sweet potato, cassava, yam, Allium spp and temperate tree species for conservation.…”
Section: Conservation Biotechnology By Bk Joshimentioning
confidence: 99%
“…Since, last 40 years, CIP has been contributed to developing tissue culture techniques for conserving potato germplasm (Withers et al, 1997).It is the most prominent and efficient way for distributing clonal materials. It ensures the availability of planting material any time and made possible the eradication of virus through meristem culture.…”
Section: Introductionmentioning
confidence: 99%