Cryopreservation of invitro-propagated protocorms of Caladenia for terrestrial orchid conservation in Western Australia
dc.contributor.author | Watanawikkit, P. | |
dc.contributor.author | Tantiwiwat, S. | |
dc.contributor.author | Bunn, E. | |
dc.contributor.author | Dixon, Kingsley | |
dc.contributor.author | Chayanarit, K. | |
dc.date.accessioned | 2017-01-30T12:35:50Z | |
dc.date.available | 2017-01-30T12:35:50Z | |
dc.date.created | 2015-10-29T04:09:40Z | |
dc.date.issued | 2012 | |
dc.identifier.citation | Watanawikkit, P. and Tantiwiwat, S. and Bunn, E. and Dixon, K. and Chayanarit, K. 2012. Cryopreservation of invitro-propagated protocorms of Caladenia for terrestrial orchid conservation in Western Australia. Botanical Journal of the Linnean Society. 170 (2): pp. 277-282. | |
dc.identifier.uri | http://hdl.handle.net/20.500.11937/23167 | |
dc.identifier.doi | 10.1111/j.1095-8339.2012.01284.x | |
dc.description.abstract |
Cryopreservation is an important tool for the exsitu preservation of endangered plants. In this article, we describe the development of a cryopreservation protocol for orchid protocorms using the terrestrial Australian species Caladenia latifolia. Protocorms of C. latifolia generated asymbiotically each month on Murashige and Skoog (MS) medium containing 10µM N6-benzyladenine (BAP) provided explant sources for cryopreservation. Three size classes of protocorms were used as source explant material [small (S, =1mm); medium (M, >1<4mm); large (L, =4mm)] in combination with five desiccation treatments, i.e. 0, 0.4, 0.6, 0.8 and 1.0M glycerol. After 2days on desiccation medium, protocorms were treated with two cryoprotectant solutions (PVS2 and PVS4 at 0°C for 15, 20, 25 and 30min) before immersion in liquid nitrogen for 1day. Protocorms were then removed from liquid nitrogen storage, warmed rapidly (in a 40°C waterbath) and placed on three recovery media: half-strength MS with 0.5µM BAP, 0.5µM 6-furfurylaminopurine (kinetin) or 0.5µM 1-phenyl-3-(1,2,3-thiadiazol-5-yl)-urea (TDZ). Protocorms on recovery media were incubated at 25°C under dark conditions and potential protocorm survival was observed at 60 and 90days using a fluorescein diacetate (FDA) test for protocorm viability. Protocorm survival was correlated significantly with explant size. Large cryopreserved protocorms had the highest potential survival rate (>90%) relative to small (<10%) and medium (70-80%) protocorms. Different desiccation media treatments did not affect significantly the survival percentage (74-92%). Similarly, changing the cryoprotectant solution and time of incubation at 0°C did not affect significantly potential protocorm survival (76-96%). Potential protocorm survival on various recovery media was not significantly different among treatments (88-100% survival). The study indicates that the cryopreservation of terrestrial orchid protocorms is technically feasible and provides a new and potentially highly beneficial tool in terrestrial orchid conservation where seed may be limited (because of species rarity), or as a means of storing and later utilizing the large surpluses of protocorms generated in propagation programmes. | |
dc.title | Cryopreservation of invitro-propagated protocorms of Caladenia for terrestrial orchid conservation in Western Australia | |
dc.type | Journal Article | |
dcterms.source.volume | 170 | |
dcterms.source.number | 2 | |
dcterms.source.startPage | 277 | |
dcterms.source.endPage | 282 | |
dcterms.source.issn | 0024-4074 | |
dcterms.source.title | Botanical Journal of the Linnean Society | |
curtin.department | Department of Environment and Agriculture | |
curtin.accessStatus | Open access via publisher |
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