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Seed germination and in vitro propagation of Dianthus fruticosus L.

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dc.contributor.author Papafotiou, M en
dc.contributor.author Stragas, J en
dc.date.accessioned 2014-06-06T06:49:02Z
dc.date.available 2014-06-06T06:49:02Z
dc.date.issued 2009 en
dc.identifier.issn 05677572 en
dc.identifier.uri http://62.217.125.90/xmlui/handle/123456789/4389
dc.relation.uri http://www.scopus.com/inward/record.url?eid=2-s2.0-70350041090&partnerID=40&md5=bba6a99efce353ee60fcc86d37078434 en
dc.subject Acclimatization en
dc.subject Micropropagation en
dc.subject Native plant en
dc.subject Plant growth regulators en
dc.subject Rooting en
dc.subject Seed germination en
dc.subject Shoot multiplication en
dc.subject.other Dianthus en
dc.subject.other Dianthus caryophyllus en
dc.title Seed germination and in vitro propagation of Dianthus fruticosus L. en
heal.type journalArticle en
heal.publicationDate 2009 en
heal.abstract Dianthus fruticosus is an endemic plant of Greece found in rocky places of the Cyclades islands Serifos, Sikinos and Folegandros. It can be used as a bedding plant ideal for rocky gardens and Mediterranean roof gardens. It can also be a groundcover plant for slope stabilization and restoration of downgraded landscapes in the Mediterranean region. In this work seed germination conditions were studied and a micropropagation method was developed. Seeds, surface-sterilized in a 15% commercial bleach water solution for 20 min, were germinated on solid half strength MS medium with 2% sucrose at 15, 20 and 25°C under 16-h photoperiod of 37.5 μmol m-2·s -1 fluorescent light. Germination was 97% at 15°C and was reduced to 47% and 13% at 20 and 25°C, respectively. Nodal explants from the in vitro germinated seedlings were cultured on solid full strength MS medium with 2% sucrose and various plant growth regulators (NAA, IBA, BA, 2iP, TDZ). In a medium containing 0.1 mg/L NAA combined with 0.5 mg/L 2iP or 0.2 mg/L BA all the explants produced shoots. The highest multiplication rate was taken in a medium with 0.1 mg/L NAA combined with 0.5 mg/L 2iP and in a medium with 0.1 mg/L IBA combined with 0.1 or 0.5 mg/L BA. In a medium with 2 mg/L IBA all the explants produced simultaneously shoots and roots. In following subcultures the highest multiplication rate was observed in a medium with 0.1 mg/L NAA combined with 0.5 mg/L 2iP. All shoots produced in various media transplanted on a medium with 2 mg/L IBA rooted very well and plantlets were successfully established ex vitro. en
heal.journalName Acta Horticulturae en
dc.identifier.volume 813 en
dc.identifier.spage 481 en
dc.identifier.epage 484 en


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