Plantlet formation from cultured inflorescences of Dactylis glomerata L.

The objective of this study was to demonstrate plantlet formation from cultured mature inflorescences of field-grown orchardgrass (Dactylis glomerata L.) plants. Whole tillers were collected and maintained in the dark at 4°C for either 19 or 25 days before panicle sections were plated on a Linsmaier and Skoog (LS) or Schenk and Hildebrandt (SH) agar medium containing 2,4-D. Generally, better results for both cell proliferation and plantlet formation were obtained with 1) large explants (many florets) on 9.1 μM 2,4-D compared to small explants (few florets) on 1.0 μM 2,4-D, 2) SH rather than LS medium and 3) when tillers were pretreated at 4°C for 25 days rather than 19 days. Chromosome counts of basal leaf cells in 94 regenerated plants showed that no plants possessed the gametic chromosome number of n=14.