Argania spinosa (L.) Skeels is an endangered plant species endemic to Morocco. In recent years, attempts to develop in vitro regeneration systems for this species were made. However, rooting and acclimatization of in vitro plants have been a bottleneck for successful propagation. In the present study, the effects of different concentrations of auxins, putrescine, silver nitrate (AgNO₃) and ammonium nitrate on the in vitro rooting of adventitious shoots of two argan genotypes “Mejji” and “R’zwa”, were evaluated. The highest rooting percentages (86.6% in “Mejji” and 84.4% in “R’zwa”) were observed on Murashige and Skoog (MS) medium modified by reducing the ammonium nitrate concentration and supplemented with 1.5 mg L⁻¹ indole-3-butyric acid (IBA), 0.5 mg L⁻¹ 1-naphthalene acetic acid (NAA), 2 mg L⁻¹ AgNO₃ and 160 mg L⁻¹ putrescine. This medium resulted in the development of a good root system after only 10 days of culture. Plantlet acclimatization was carried out using different substrate mixtures, and high survival rates (100%) were observed when the substrate contained either peat alone or a sand–peat mixture (1:1, w/w). The high percentages of rooting and acclimatization reported in the present study are of high importance for rapid and large-scale propagation of this endangered species.

Morocco is considered one of the main biodiversity hotspots in the Mediterranean region and contains various plant species including wild and domestic Rosa. This genus is the most important among cultivated ornamental plants in the world, with a high economic value in cosmetics, pharmaceutical industries, and floriculture. In the present study, genetic diversity among the collected accessions of wild Rosa species in Morocco was assessed using Inter-Simple Sequence Repeat (ISSR) and Directed Amplification of Minisatellites DNA (DAMD) markers. Results confirmed that both markers used have a good efficiency to assess genetic diversity in wild roses. Ten ISSR and eight DAMD primers amplified 276 and 203 loci, with an average of 27.4 and 25 polymorphic alleles per primer, respectively. The polymorphic information content (PIC) values were 0.34 with ISSR and 0.31 with DAMD. Analysis of molecular variance (AMOVA) showed that genetic variation in wild rose occurs mainly within populations (86%) rather than between populations (14%). The region of Azrou (Middle Atlas of Morocco) is the area that registered the highest genetic diversity in the present study with He = 0.21. The 39 rose accessions were divided into three main groups with among-group similarity of 30%. Principal component analysis and the hierarchical classification were consistent with genetic relationships derived by structure analysis. The findings revealed that the patterns of grouping are weakly correlated with geographical origin. ISSR and DAMD markers showed that the accessions have a good genetic diversity.

Two bulbous plant species, Squilla maura and Oncostema peruviana (Asparagaceae), show particularly interesting ornamental and medicinal characteristics. Micropropagation could be a promising alternative method to accelerate their naturally slow spreading pattern. This study focused on the effects of different growth regulators and culture media on callus induction and shoot regeneration, from which an effective protocol was established. Leaf explants were cultured on Murashige and Skoog (MS), MS/2, or B5 medium, containing one auxin—1-Naphthaleneacetic acid (NAA), 2,4-Dichlorophenoxyacetic acid (2.4-D), or 3-indolebutyric acid (IBA)—combined with the cytokinin 6-Benzylaminopurine (BAP), at various concentrations. All treatments resulted in callogenesis rates between 65–100% for both species. These treatments led to direct bulbil regeneration. Among the treatments, the B5 medium with 1 mgL⁻¹ BAP and 1 mgL⁻¹ 2,4-D gave the highest regeneration rate (89.2%) for O. peruviana, while the ½MS medium with 0.5 mgL⁻¹ BAP and 0.5 mgL⁻¹ NAA showed the highest regeneration rate (85.5%) for S. maura. The highest mean number of bulils per explant was 7.44 for O. peruviana on the MS medium (0.5 mgL⁻¹ BAP and 2 mgL⁻¹ IBA), and 9.5 for S. maura on the MS medium (1 mgL⁻¹ BAP and 0.5 mgL⁻¹ NAA). The regenerated bulbils were transferred for multiplication to the MS medium with a hormone combination (2 mgL⁻¹ BAP and 0.2 mgL⁻¹ NAA) which increased the multiplication rate compared to the callus induction me dium, with a highest recorded multiplication rate of 177 (O. peruviana) and 104.33 (S. maura). The propagation stage achieved the highest number of bulbils/explant after a second subculture for the two species. An efficient micropropagation protocol was established for S. maura, which answers our main objective, and it would contribute to their conservation and sustainable use in ornamental and medicinal applications.