Comparing nuclear DNA content, pollen viability, pollen production and seed retention of lavender and lavandin

Year 2024, Volume: 37 Issue: 2, 85 - 90, 02.08.2024

Hasan Baydar , Ümmü Tuğlu

https://doi.org/10.29136/mediterranean.1425089

Abstract

Lavender (Lavandula spp.) is one of the most widely grown essential oil crops in the world. This study aimed to determine the nuclear DNA contents using flow cytometry, pollen viability using TTC (2,3,5-Triphenyl Tetrazolium Chloride) and IKI (Iodine Potassium Iodide) tests, pollen production quantities using hemacytometric method, and seed retention rates per spike and flower of lavender (L. angustifolia var. Raya) and lavandin (L. intermedia var. Super) grown under ecological conditions in Isparta province of Turkey. The nuclear DNA contents were 2.11 and 2.54 pg 2C-1, respectively in the lavender and lavandin cultivar. The flowers of the lavender cultivar produced abundant pollen grains (average 5800 pollen per flower and 1450 pollen per anther) with high viability (60.65-65.05%) and seed retention rate per spike (91.57% on average). The lavandin cultivar, which had very low pollen viability (1.08-3.32%) and pollen grains (average of 2350 pollen per flower and 587.5 pollen per anther) gave very low seed retention rates per spike (0.60% on average). While each flower had four ovaries with the potential to produce four nutlets, lavandin flowers produced only trace numbers (0.15% on average) of seeds. As a result, the lavandin cultivar had more nuclear DNA content, longer stem and spike, smaller size but more numerous flowers, less and lighter anthers, lower pollen grains and viability, and vey few inviabile seeds compared to the lavender cultivar. It has been observed by eye that honey bees do not visit lavender and lavandin flowers for collecting pollen, but solely for collecting nectar.

Keywords

Lavender, Lavandin, Flow cytometer, Pollen viability, Seed retention

Ethical Statement

This article does not contain any studies with human participants or animals performed by any of the authors.

Thanks

We would like to thank Prof.Dr. Metin Tuna from Tekirdağ Namık Kemal University for flow cytometry analysis.

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