2005
DOI: 10.1079/ivp2004596
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Cryopreservation of chestnut by vitrification of in vitro-grown shoot tips

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Cited by 30 publications
(26 citation statements)
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“…The cold storage of cultures represents a procedure for medium-term conservation, and Janeiro et al ( 1995 ) reported the possibility of keeping chestnut cultures at 2-4°C for up to 1 year without subculture. In addition, a successful cryopreservation system of chestnut shoot tips has been reported (Vidal et al 2005 ) allowing long-term storage of chestnut genotypes in liquid nitrogen. A detailed protocol for micropropagation of European chestnut, including storage and molecular marker analysis to determine the genetic stability of in vitro regenerated plants, has recently been published ) .…”
Section: Propagationmentioning
confidence: 99%
“…The cold storage of cultures represents a procedure for medium-term conservation, and Janeiro et al ( 1995 ) reported the possibility of keeping chestnut cultures at 2-4°C for up to 1 year without subculture. In addition, a successful cryopreservation system of chestnut shoot tips has been reported (Vidal et al 2005 ) allowing long-term storage of chestnut genotypes in liquid nitrogen. A detailed protocol for micropropagation of European chestnut, including storage and molecular marker analysis to determine the genetic stability of in vitro regenerated plants, has recently been published ) .…”
Section: Propagationmentioning
confidence: 99%
“…The vitrification-based procedure described by Vidal et al (2005) was applied to 46 genotypes (Table 1) of the 130 genotypes established in vitro. The number of shoot apices cryopreserved per genotype varied from 90 to 300, and was related to the proliferation capacity of each genotype.…”
Section: Cryopreservation Of Chestnut Shoot Tipsmentioning
confidence: 99%
“…Finally, the cryopreservation of embryogenic cultures from mature cork oak material was also found to be feasible, with high levels of embryo recovery recorded (88-93%) (Valladares et al 2004). Cryopreservation of chestnut shoot apices from in vitro cultures multiplied through axillary shoots was also reported as an alternative to preservation of zygotic embryo axes and somatic embryos (Vidal et al 2005).…”
Section: Introductionmentioning
confidence: 99%
“…In C. sativa, Vidal et al [115] and Jorquera et al [116] investigated the possibility of cryopreserving shoot tips from material of juvenile and adult origin excised from in vitro cultures using the vitrification process. The shoot recovery percentages varied between 33-54% depending on the genotype, although these differences did not appear to be related to the juvenile or adult status of the material.…”
Section: Long-term Preservation (Cryopreservation)mentioning
confidence: 99%