An effective protocol for in vitro germination and seedling development of lentisk (Pistacia lentiscus L.)

dc.authorid0000-0003-3480-6013en_US
dc.contributor.authorYıldırım, Hakan
dc.contributor.authorÇalar, Nazan
dc.contributor.authorOnay, Ahmet
dc.date.accessioned2021-06-01T08:38:37Z
dc.date.available2021-06-01T08:38:37Z
dc.date.issued2018en_US
dc.departmentMTÖ Üniversitesi, Ziraat Fakültesi, Bahçe Bitkileri Bölümüen_US
dc.description.abstractDifferent nutrient media (MS [Murashige and Skoog 1962]; QL [Quoirin and Lepoivre 1977] and WPM [Lloyd and McCown 1980]); plant growth regulators BA (benzil adenin), GA3 (gibberellic acid), IBA (indole-3-butyric-acid), NAA (naftalen acedic acid); and sucrose concentrations were studied to determine the in vitro culture effects on healthier and faster seedling development from mature lentisk (Pistacia lentiscus L.) seeds. After 28 days of culture, the percentage of germinated seeds was the highest (70%) in the full-strength MS medium. The cytokinin BA was superior to other tested treatments in terms of its ability to promote germination of lentisk seeds. When tested at different concentrations, sucrose gave the best results obtained at concentrations of 1–4%, whereas high concentrations (6 and 8%) mainly decreased germination rate and there was no a regular pattern for elongation of the aerial parts of plants. With this described protocol, on average 76.67% seeds germinated 4 weeks after culture. Developed seedlings were satisfactorily acclimatized in sterilized peat, soil and perlite containing compost, with high percentage survival viability was obtained 9 months after transfer to in vivo conditions (93.33%). The results obtained showed that the enriched full-strength MS medium supplemented with 1 mg L–1 BA and 3% sucrose induced homogeneous and healthy seedling development in a period of 4 to 8 weeks of culture.en_US
dc.identifier.citationYıldırım, H., Çalar, N., Onay, A. (2018). Aneffectiveprotocolforin vitrogermination andseedlingdevelopmentoflentisk (Pistacia lentiscus L.). Acta Sci. Pol. Hortorum Cultus, 17(4), 3–13. DOI: 10.24326/asphc.2018.4.1en_US
dc.identifier.doi10.24326/asphc.2018.4.1
dc.identifier.endpage13en_US
dc.identifier.issn1644-0692en_US
dc.identifier.issn2545-1405en_US
dc.identifier.issue4en_US
dc.identifier.scopus2-s2.0-85053279790en_US
dc.identifier.scopusqualityQ3en_US
dc.identifier.startpage3en_US
dc.identifier.urihttps://doi.org/10.24326/asphc.2018.4.1
dc.identifier.urihttps://hdl.handle.net/20.500.12899/165
dc.identifier.volume17en_US
dc.identifier.wosWOS:000442777800001en_US
dc.identifier.wosqualityQ4en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.institutionauthorYıldırım, Hakan
dc.language.isoenen_US
dc.publisherWydawnictwo Akad Rolniczej W Lublinieen_US
dc.relation.ispartofActa Scientiarum Polonorum, Hortorum Cultusen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectMastic treeen_US
dc.subjectMicropropagationen_US
dc.subjectSeeden_US
dc.titleAn effective protocol for in vitro germination and seedling development of lentisk (Pistacia lentiscus L.)en_US
dc.typeArticleen_US

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