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Seed germination and in vitro propagation of Sideritis athoa

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dc.contributor.author Papafotiou, M en
dc.contributor.author Kalantzis, A 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/123456789/4390
dc.relation.uri http://www.scopus.com/inward/record.url?eid=2-s2.0-70350056565&partnerID=40&md5=f775f715ec636288f66447089e95bb5f en
dc.subject Hyperhydration en
dc.subject Micropropagation en
dc.subject Native plant en
dc.subject Plant growth regulators en
dc.subject Rooting en
dc.subject Shoot multiplication en
dc.subject Vitrification en
dc.subject.other Sideritis en
dc.subject.other Sideritis athoa en
dc.title Seed germination and in vitro propagation of Sideritis athoa en
heal.type journalArticle en
heal.publicationDate 2009 en
heal.abstract Sideritis athoa is an alpine, aromatic perennial herb, and a native plant of Greece that could be introduced as a bedding plant, a plant for rock gardens, roof gardens, restoration of degraded landscapes and to maintain slope stability. S. athoa seeds were collected in August and germinated in November in vitro or on peatperlite (1:1 v/v) or 100% perlite media. Seeds were placed onto a solid half strength MS medium with 20 g/L sucrose and held at 10, 15, 20 or 25°C either under continuous darkness or 16-h photoperiod (37.5 μmol·m-2·sec-1 fluorescent light). Germination at 20°C was high independent of substrate and light. The highest germination (80-88%) was obtained for seeds planted on peat-perlite or 100% perlite at 20°C. On MS medium germination was slightly lower and delayed. Nodal explants from in vitro grown seedlings were cultured on solid MS with 8 g/L agar and 20 g/L sucrose supplemented with various plant growth regulators (BA, 2iP, TDZ, NAA, IBA) in order to induce shoot regeneration. The highest shoot numbers were obtained in media with BA (0.2, 0.5 or 1.0 mg/L) (2.3-2.5 shoots per explant, 0.6 cm long). The addition of NAA to the BA-media reduced the production of shoots and induced callus and shoot malformation. Callus and malformations were observed in TDZ-media, while the 2iP-media gave low shoot production. The medium with 1 mg/L IBA produced fewer but longer shoots compared to BA-media (1.5 shoots per explant, 2 cm long). Nodal explants from in vitro produced shoots were initially successfully subcultured for multiplication on media with 0.2 mg/L BA with or without 0.1 mg/L IBA. However, in subsequent subcultures, many shoots were hyperhydrated. Increased agar (12 or 20 g/L) or sucrose (30 g/L) concentrations eliminated hyperhydration. Microshoots held on IBA (2 mg/L) alone or with NAA (1 mg/L) gave the best rooting in terms of percentage (46% or 53%, respectively) and root quality. en
heal.journalName Acta Horticulturae en
dc.identifier.volume 813 en
dc.identifier.spage 471 en
dc.identifier.epage 476 en


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