In order to analyze the extent to which allelopathic action of Cistus ladanifer may influence the successional progression towards Mediterranean sub-climacic shrublands and the geographical distribution of other species, the inhibitory effect of Cistus ladanifer extracts on the germination of 20 Mediterranean species was analyzed. Five of the species tested were characteristic of maquis sub-climacic shrublands: Arbutus unedo, Adenocarpus argyrophyllus, Phillyrea angustifolia, Phillyrea latifolia, and Rhamnus alaternus. Tests were also carried out on 6 Cistaceae species in order to evaluate the auto-toxicity rate of allelopathic extracts: Halimium umbellatum subsp. viscosum, Halimium ocymoides, Cistus ladanifer, Cistus salvifolius, Cistus monspeliensis, and Cistus populifolius. Nine herbaceous species sharing the natural habitat with C. ladanifer were also examined. Results confirmed a clear inhibitory and delaying effect of aqueous C. ladanifer-leaf extracts on the germination of P. angustifolia, P. latifolia, R. alaternus, H. ocymoides, C. populifolius, Erysimum lagascae, Brassica barrelieri, Silene tridentata, and Moricandia moricandioides. Assays with soil collected below the canopy of the C. ladanifer community showed more pronounced inhibitory effect on sub-climacic shrub species than the aqueous extracts. In contrast, the opposite pattern was detected when analyzing the allelopathic effect of natural soil on Cistaceae and herbaceous species. Allelopathic compounds produced by C. ladanifer showed little auto-toxicity. The inhibitory effect of phytotoxic compounds accumulated in the jaral soil upon germination of A. unedo, B. barrelieri, and M. moricandioides was eliminated by heating soil at 150°C for 10 min. Phenolic compounds (i.e. ferulic, p-hydroxybenzoic, vanillic, p-coumaric, and caffeic acids) and terpenes (i.e.a and b-pinene) with allelopathic documented effect were detected in the aqueous extracts and soil samples used in the analyses. We suggest that the allelopathic effect of C. ladanifer may influence the composition and structure of Mediterranean communities where the species is present, since it hinders the establishment of some sub-climacic species and may reduce the area occupied by numerous herbaceous species.

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Seeds of Aconitum napellus subsp. castellanum were physiologically dormant at maturity in early autumn, with underdeveloped embryos. Thus they have morphophysiological dormancy (MPD). Embryos in fresh seeds were on average 1.01 mm long, and they had to grow to 3.60 mm before radicle emergence. Cold stratification at 5°C for 5 months with light enhanced the mean embryo length to 2.73 mm (SE = 0.13) and seed germination to 20%. However, with higher temperatures (15/4, 20/7, 25/10, 28/14 and 32/18°C) embryo growth was small, with no seeds germinating. Optimal germination was achieved after 4 months of cold stratification at 5°C followed by incubation at 20/7°C for 1 month with light, when germination ranged between 70 and 79%, depending on seed age, locality and year of collection. Cold stratification could be substituted by the application of GA3 solution, since mean embryo length in seeds incubated at 25/10°C for 1 month with light was 3.52 mm and the germination was 80%. Since cold stratification was the only requirement for the loss of MPD, the longest embryo growth occurred during this treatment, and GA3 promoted MPD loss, we concluded that A. napellus seeds have intermediate complex MPD. Germination was higher in 4-month stored than in freshly matured seeds. A pronounced variability in germinative patterns at inter-annual and inter-population level was recorded.

The main goal of the study was to assess germination requirements in a threatened daffodil to elaborate a detailed protocol for plant production from seeds, a key tool for conservation. Experiments were carried out both in the laboratory and outdoor conditions. In Pseudonarcissi section, endemic Iberian species of Narcissus studied heretofore have different levels of morphophysiological dormancy (MPD). Embryo length, radicle emergence, and shoot emergence were analyzed to determine the level of MPD. Both interpopulational variability and seed storage duration were also studied. Mean embryo length in fresh seeds was 1.32 mm and the embryo had to grow until it reached at least 2.00 mm to germinate. Embryo growth occurs during warm stratification, after which the radicle emerges when temperatures go down. Seed dormancy was broken in the laboratory at 28/14°C in darkness followed by 15/4°C, but the germination percentage varies depending on the population. In outdoor conditions, seed dispersal occurs in June, the embryo grows during the summer and then the radicle emerges in autumn. The radicle system continues to grow during the winter months, but the shoot does not emerge until the beginning of the spring because it is physiologically dormant and requires a cold period to break dormancy. Early cold temperatures interrupt embryo growth and induce dormancy in seeds with an advanced embryo development. Seeds of N. eugeniae have deep simple epicotyl MPD. In addition, we found that embryo growth and germination were improved by seed storage duration.