2007
DOI: 10.1071/bt06065
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The contribution of in vitro technology and cryogenic storage to conservation of indigenous plants

Abstract: In vitro culture has enabled a variety of recalcitrant and threatened plant taxa to be micropropagated in the absence of viable conventional propagation methods. Cryogenic storage research has provided alternative protocols for efficient long-term germplasm storage for many plant species. Recent advances in tissue-culture methods such as somatic embryogenesis have enabled the production of >20 000 somatic embryos of a recalcitrant native Australian rush in a few months, far higher than other in vitro method… Show more

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Cited by 50 publications
(41 citation statements)
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“…× E. rudis Endl. [162], 0.25, 2.5, or 5 µM IBA with 0.25 or 0.5 µM NAA for E. impensa [70], and 2.5 µM IBA with 2.5 µM NAA for E. sideroxylon [85]. NAA has been used alone to induce roots at 10.8 µM for C. citriodora [69], 2.7 µM for E. grandis and E. grandis × E. urophylla [124], 1.1 or 2.7 µM for E. pellita [100], and 12.5 µM for E. urophylla × E. grandis [163].…”
Section: Adventitious Root Formationmentioning
confidence: 99%
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“…× E. rudis Endl. [162], 0.25, 2.5, or 5 µM IBA with 0.25 or 0.5 µM NAA for E. impensa [70], and 2.5 µM IBA with 2.5 µM NAA for E. sideroxylon [85]. NAA has been used alone to induce roots at 10.8 µM for C. citriodora [69], 2.7 µM for E. grandis and E. grandis × E. urophylla [124], 1.1 or 2.7 µM for E. pellita [100], and 12.5 µM for E. urophylla × E. grandis [163].…”
Section: Adventitious Root Formationmentioning
confidence: 99%
“…However, adventitious rooting on eucalypt shoots is usually induced with an auxin rooting hormone, typically IBA at a concentration between 0.49 and 49 µM (Table A1). IBA has also been used in combination with NAA to induce adventitious eucalypt roots, including 5 µM IBA with 0.5 or 1.0 µM NAA for E. dolorosa Brooker & Hopper [162], 0.25 µM IBA with 0.25 µM NAA, or 0.5 µM IBA with 0.5 µM NAA, for E. drummondii Benth. × E. rudis Endl.…”
Section: Adventitious Root Formationmentioning
confidence: 99%
“…However, several in vitro and tissue culture techniques have been known for its conservation properties by maintaining the genetic homogeneity of the regenerated plantlets from the stored germplasms (Engelmann 2012) as these techniques confirmed the mid-term storage of plant materials ensuring higher germination rates (Bunn et al 2007). But on the other side for long-term storage of plant germplasms, cryopreservation is the lone technique.…”
Section: Forest Seeds: Concernsmentioning
confidence: 99%
“…Tissue culture techniques are of great interest for collecting, multiplication and storage of plant germplasm and are very useful for conserving plant biodiversity, including (a) genetic resources of recalcitrant seed and vegetatively propagated species; (b) rare and endangered plant species; and (c) biotechnology products, such as elite genotypes and genetically engineered material [6,31,32]. Tissue culture systems allow propagating plant material with high multiplication rates in an aseptic environment.…”
Section: In Vitro Technologies For Propagation and Exchange Of Plant mentioning
confidence: 99%
“…There are several examples to illustrate the application of cryopreservation techniques above described to preserve rare and endangered species for various higher plants [32], including orchids [118], bryophytes and ferns [119].…”
Section: Long-term Conservation Through Cryopreservationmentioning
confidence: 99%