Parisa Jonoubi, Ahmad Majd, Aref Marouf, Shahla Amini,
Volume 2, Issue 3 (12-2015)
Abstract
Pimpinella anisum L. belongs to Apiaceae family. The samples of vegetative and reproductive organs at different stages of development were gathered and investigated by cell-histology methods. The investigation of the anatomical structure of vegetative organs showed that the secretory ducts are arranged between the parenchymal tissues of the leaf. Section of flower buds revealed that anthers had 4 pollen sacs, the division of pollen mother cell was of the simultaneous type, microspore tetrads were of tetragonal type and the tapetum layer was secretory. The study of the ultrastructure of pollen grains with SEM showed that they had 3 pores. The ovary was found to be two-chambered and two-carpeled the ovule to be anatropous and to have one membrane. In embryogenic investigation it was found that the embryos were globular, cotyledonary and torpedo-shaped and the transition between globular embryos to cordate embryos was found. The vegetative organs were observed to have the general structure of dicotyledons. The development patterns of ovule and embryo sac follow the Polygonum type. Tetrahedral microspore tetrads were observed. The ultrastructure of pollens was found to be similar to those of Smyrnium, a genus of Apiaceae family. All stages of embryogenesis were covered in this study.
Parissa Jonoubi, Majid Ghorbani Nohooji, Halimeh Hassanpour, Atefeh Ashourisheikhi,
Volume 12, Issue 2 (9-2025)
Abstract
Ferula gummosa Boiss. as a valuable pharmaceutical and industrial plant grows in Iran. In order to minimize seed dormancy period and micropropagation, callus induction and embryogenesis were evaluated. The plantlets of the seeds were separated and cultured in the 1/2 MS medium. After 14 days, root, hypocotyl, cotyledon and leaf explants were separated. Then they were transferred to the basal MS medium containing different concentrations of growth regulators. Different developmental stages of somatic embryos were evaluated. Seedlings 2-3 days after locating in 1/2 MS medium germinated and whole plantlets were obtained after 12 days. In the callus induction phase growth regulator composition 1.5 mgl-1 of NAA and 0.5 mgl-1 of BA with root explants had proper results. In the somatic embryogenesis phase MS medium containing 0.5 mgl-1 of 2,4-D accompanied by 1 mgl-1 of BA lead to desirable results. Via taken sections from the embryos, different developmental stages of somatic embryos including pre-embryo, globular, heart shaped, torpedo and cotyledonary embryo were observed. In vitro culture of embryo to accelerate germination and elimination of long dormancy period and using this optimized method are strongly suggested for micropropagation of this plant so this valuable endemic plant may survive from extinction, too.
