Abstract:The establishment phase is an important bottleneck in the life cycle of plants. It consists of two steps that are rarely separated, i.e., the germination of seeds and the establishment of seedlings. Here we report the results of two experiments in which we independently investigated germination and seedling establishment in the greenhouse, under different grass vegetation treatments representing different regeneration niches. Seeds of Tragopogon pratensis from six populations and two habitat types were studied… Show more
“…In Clarkia species, germination ability did not exhibit local adaptation, but postgermination survival did, although it is not clear the extent to which variation in germination phenology contributed to those differences in survival (Geber & Eckhart 2005). In Tragopogon pratensis, seeds from roadside populations germinated faster and to higher percentages when grown in roadside locations than did those from nonroadside populations ( Jorritsma-Wienk et al 2007). Bromus tectorum showed local adaptation in germination, operating through seedling survival, in low-elevation sites but not high-elevation sites (Leger et al 2009), andSzarek et al (1998) reported local adaptation in germination in Encelia farinose.…”
Section: Evidence Of Local Adaptation In Germinationmentioning
confidence: 95%
“…In Centaurea, burnt soil inhibited germination, even though the nutrient release from burning increased seedling growth; however, seedlings also grew better in shade, which would be eliminated by fire (Riba et al 2002). In other examples, germination showed some evidence of adaptation in terms of germination percentages, but seedling performance did not ( Jorritsma-Wienk et al 2007). In some cases, seeds tended to germinate in environments that were actually less favorable for seedling survival.…”
Section: The Integrated Organism: Associations Between Germination Anmentioning
Germination behavior is one of the earliest phenotypes expressed by plants. This fact has several consequences for the evolution of postgermination traits, ecological niches, and geographic ranges. By determining the conditions that plants experience after they germinate, germination influences phenotypic expression of postgermination traits, natural selection on them, and their genetic basis. The breadth of germination niches may influence the ecological breadth and geographic ranges of species. Because germination is expressed early, it is frequently subjected to natural selection before other traits are expressed. We review evidence for natural selection on and adaptation of germination and discuss how the breadth of the germination niche is associated with the ecological niche and range of plant species. We review evidence for the coevolution of germination and postgermination traits and compare germination to postgermination niches. Finally, we discuss how germination responses to altered environments can influence species distribution and the evolution of postgermination traits after environmental change.
“…In Clarkia species, germination ability did not exhibit local adaptation, but postgermination survival did, although it is not clear the extent to which variation in germination phenology contributed to those differences in survival (Geber & Eckhart 2005). In Tragopogon pratensis, seeds from roadside populations germinated faster and to higher percentages when grown in roadside locations than did those from nonroadside populations ( Jorritsma-Wienk et al 2007). Bromus tectorum showed local adaptation in germination, operating through seedling survival, in low-elevation sites but not high-elevation sites (Leger et al 2009), andSzarek et al (1998) reported local adaptation in germination in Encelia farinose.…”
Section: Evidence Of Local Adaptation In Germinationmentioning
confidence: 95%
“…In Centaurea, burnt soil inhibited germination, even though the nutrient release from burning increased seedling growth; however, seedlings also grew better in shade, which would be eliminated by fire (Riba et al 2002). In other examples, germination showed some evidence of adaptation in terms of germination percentages, but seedling performance did not ( Jorritsma-Wienk et al 2007). In some cases, seeds tended to germinate in environments that were actually less favorable for seedling survival.…”
Section: The Integrated Organism: Associations Between Germination Anmentioning
Germination behavior is one of the earliest phenotypes expressed by plants. This fact has several consequences for the evolution of postgermination traits, ecological niches, and geographic ranges. By determining the conditions that plants experience after they germinate, germination influences phenotypic expression of postgermination traits, natural selection on them, and their genetic basis. The breadth of germination niches may influence the ecological breadth and geographic ranges of species. Because germination is expressed early, it is frequently subjected to natural selection before other traits are expressed. We review evidence for natural selection on and adaptation of germination and discuss how the breadth of the germination niche is associated with the ecological niche and range of plant species. We review evidence for the coevolution of germination and postgermination traits and compare germination to postgermination niches. Finally, we discuss how germination responses to altered environments can influence species distribution and the evolution of postgermination traits after environmental change.
“…The major reason of this variation during autumn and winter appeared to be seedlings mortality caused by both abiotic and biotic stresses such as cold temperatures, soil drought and intraspecific competition (Harper and McNaughton, 1962;Jorritsma-Wienk et al, 2007;White and Harper, 1970). Anyway, two years after sowing, only C.…”
The use of native species in landscape design is a choice related to environmental sustainability and it contributes to the aesthetic appeal of urban and marginal areas. However, to date, the lack of knowledge of the ecological characteristics and agronomic practices of these species, represents a limit for their use. This study aims to obtain information about germination ecology, morphological traits and ornamental value of 7 selected perennial native taxa, with potential use in meadows seed mixtures for the Mediterranean environment. Seed germination for each taxon was assessed under different conditions (temperature, photoperiod and pre-treatment) in a controlled environment, while data on plant performances was collected from field plots. In general, the dormant seeds showed a positive response to pre-treatment with gibberellic acid (GA 3 ) and chilling within a period of about six months from the time of seed collection. The dependence of germination on light and temperature was observed in most of the tested taxa.Differences in plant height and flowering dynamics gave practical directions in terms of combining seeds of different species to create and maintain a wildflower meadow in lowmaintenance areas. Crepis bursifolia L. and Hypochaeris radicata L. were the only two species which showed good persistence during the two-year field study and met the aesthetic requirements of low-input Mediterranean landscaping. Our study by adding original findings to the limited knowledge available on wildflower sowing in the Mediterranean environment,contributes to the development of sustainable strategies in the greening projects designed for those peculiar climatic conditions.
“…In this respect, Jorritsma-Wienk et al (2006) andJongejans et al (2006) argue that the establishment phase represents the most important bottleneck in the life cycle of the plant species, which is divided into two parts: seed germination and plant survival. After successful establishment, positive (facilitation) and negative (competition) interaction play an important role in driving the overall plant species' assemblage (Callaway 2007).…”
Over the last 20 years, the species assemblage of the species-rich dry grassland communities of central Germany has changed due to the ongoing abandonment of traditional land-use practices. In our study we wanted to investigate the germination biology and the plant-plant interaction of the low-growing and declining forb Alyssum montanum and the increasingly dominant grass Festuca rupicola. To investigate the germination behaviour we simulated cold (8/4°C), warm (20/10°C) and hot (32/20°C) conditions under a light-dark regime (12/12 hours) as well as in constant darkness. Germination of both species was similar with almost all non-dormant seeds germinating under intermediate temperature conditions (20/10°C). Whereas F. rupicola (F) germinated equally well under light changing conditions and constant darkness, the germination of A. montanum (A) was clearly reduced in darkness, which implies a strong competitive advantage of F. rupicola in dense vegetation cover. However, A. montanum germinated early under all temperatures regimes and better under 20/10°C as well as with light changing conditions. The interactions between the two species were tested in a pod-experiment with a replacement design, within which the composition of individuals was changed in the following way: 4A/1F, 3A/2F, 2A/3F, 1A/4F (eight replications per each). To evaluate any influence of intraspecific competition we created monocultures in an additive design (1A, 2A, 3A, 4A, 5A, 1F, 5F; eight replications per each). Despite that A. montanum developed faster and flowered after only four months in the replacement design experiment, the herb responded negatively to the presence of F. rupicola in several parameters (number of flowers, number of fruits and biomass per individual). The calculation of the Relative Neighbour Effect (RNE) indicated facilitation for F. rupicola and competition on A. montanum, which increased with increasing number of individuals of the other species. Our data suggest that A. montanum seedling recruitment, growth and fitness are negatively affected by increasing vegetation density of the expanding grass species F. rupicola.
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