To define the preliminary embryogenesis culture conditions of Moroccan Cork Oak (Quercus suber L.) in secondary propagation systems, secondary embryos formation from primary embryos were analyzed using seven macronutr...To define the preliminary embryogenesis culture conditions of Moroccan Cork Oak (Quercus suber L.) in secondary propagation systems, secondary embryos formation from primary embryos were analyzed using seven macronutrient medias: (Chalupa) (BTM), Murashige and Skoog (MS), Schenk and Hildebrant (SH), Schenk and Hildebrant with half content macronutrients (SH ?), full Gamborg (G), Margara (N30K) and Woody Plant Media(WPM). Mature primary embryos at cotyledonal stage of 8 - 10 mm, were placed in each culture medium, and supplemented with 30 g/l of glucose and 7 g/l of agar without PGR. The experimental design consisted of a Petri dish containing three embryos explants. Each one of the seven treatments was composed of ten Petri dishes. Mean number of secondary somatic embryos, clusters and new embryogenic formation on clusters were recorded after 8 weeks, and evaluated by statistical analysis. There were no significant differences (p ≤ 0.05) in clusters and new embryos on clusters formation among evaluated media;but mean number of secondary embryos was significantly higher in N30K (4.37 ± 0.48) compared with control media (1.37 ± 0.15). The morphology of secondary embryos grown in the N30K medium exclusively showed the presence of three embryogenic stages: early cotyledonal with translucide aspect, white opaque, or green, and mature embryos. These results indicate that the medium do influence the morphogenic characteristics of produced embryos. Our finding revealed that secondary somatic embryos produced in N30K medium presented better morphogenic potential, with different stages of embryogenic formation.展开更多
文摘To define the preliminary embryogenesis culture conditions of Moroccan Cork Oak (Quercus suber L.) in secondary propagation systems, secondary embryos formation from primary embryos were analyzed using seven macronutrient medias: (Chalupa) (BTM), Murashige and Skoog (MS), Schenk and Hildebrant (SH), Schenk and Hildebrant with half content macronutrients (SH ?), full Gamborg (G), Margara (N30K) and Woody Plant Media(WPM). Mature primary embryos at cotyledonal stage of 8 - 10 mm, were placed in each culture medium, and supplemented with 30 g/l of glucose and 7 g/l of agar without PGR. The experimental design consisted of a Petri dish containing three embryos explants. Each one of the seven treatments was composed of ten Petri dishes. Mean number of secondary somatic embryos, clusters and new embryogenic formation on clusters were recorded after 8 weeks, and evaluated by statistical analysis. There were no significant differences (p ≤ 0.05) in clusters and new embryos on clusters formation among evaluated media;but mean number of secondary embryos was significantly higher in N30K (4.37 ± 0.48) compared with control media (1.37 ± 0.15). The morphology of secondary embryos grown in the N30K medium exclusively showed the presence of three embryogenic stages: early cotyledonal with translucide aspect, white opaque, or green, and mature embryos. These results indicate that the medium do influence the morphogenic characteristics of produced embryos. Our finding revealed that secondary somatic embryos produced in N30K medium presented better morphogenic potential, with different stages of embryogenic formation.
