Summary1. When range shifts or invasions of plant species are studied, it is important to know whether large-scale spatial variation in a species' demography can be ignored or approximated by variation observed over smaller spatial scales. 2. Here, we studied the population dynamics of three similar (as shown by elasticity analysis) shortlived perennial plant species in multiple sites in different European countries over 2 years. We constructed a total of 40 transition matrices and analysed the spatio-temporal variation in the projected population growth rate (k) with spatially nested life table response experiments (LTRE). 3. All species (Carlina vulgaris, Tragopogon pratensis and Hypochaeris radicata) showed considerable life-history variation among regions on top of variation among sites within regions. 4. Net variance contributions (NVC), a novel LTRE statistic, revealed that in each species, variation in one group of vital rates contributed most to variation in k among regions as well as among sites. However, that most important type of vital rates differed between species: plant growth in C. vulgaris, flower head production in T. pratensis and establishment probability of seedlings in H. radicata. The rankings of the NVCs of other vital rates varied between site and region effects, suggesting that buffering through negative vital rate correlations varies over different spatial scales, while the identity of the main contributor to k variation is more constant. 5. Temporal effects were smaller than spatial effects, but the LTREs showed strong interactions between time and space (region or site), suggesting that the effect of, e.g. climate fluctuations are not synchronized throughout the distribution of a species. 6. Synthesis. This study shows that the life histories of plant species are distinguishable even when mean elasticity values show only small differences, and that life histories vary over the distribution range of a species. Demographic differences over large spatial scales can therefore only be partly substituted by small scale spatial variation in modelling studies on the population dynamics of a species across its entire distribution.

Many studies have focused on the ecology of seed dimorphism, the production of two seed types by a single plant. Morphology and seed size are usually correlated, but how morphology affects germination percentage and seedling growth is poorly understood. Here we explicitly separate these effects for nine populations of the dimorphic species Tragopogon pratensis subsp. pratensis. Larger seeds yielded higher germination percentages, yet seed morphology had no additional direct effect on germination. Neither seed size nor seed morphology affected seedling growth. Neither germination nor seedling growth varied among populations, but seed head varied significantly. Results show that germination is mainly controlled by seed size rather than by seed morphology. This study is one of the few to distinguish explicitly between seed size and seed morphology effects on ecological characteristics and suggests that seed dimorphism may exert its ecological effects predominantly through its correlated size.

Adaptation to the specific conditions at different sites may contribute strongly to the wide distribution of a plant species. However, little is known about the scale at which such adaptation occurs in common species. We studied population differentiation, plasticity and local adaptation of the short-lived perennial Hypochoeris radicata, a widespread and common plant whose seeds are well-dispersed. We reciprocally transplanted seedlings among several populations of different size within and among three European regions (in the northwest Czech Republic, central Germany and the central Netherlands) and studied several fitness-related traits over two growing seasons. The region in which the reciprocal transplant experiment was carried out had no influence on the performance of seedlings, indicating that there were no differences in overall habitat quality. In contrast, the site within region, and the plot within site strongly influenced mean plant performance. Plants from different populations of origin differed in their performance, indicating genetic variation among populations, but performance strongly depended on the specific combination of population of origin and transplant site. Plants that grew at their home site produced on average almost twice the number of seeds per transplant (a multiplicative fitness measure) than foreign plants originating from other sites. Survival, rosette size and multiplicative fitness all decreased with increasing distance from the home site to the transplant site. The size of the population of origin did not influence overall plant performance or the strength of local adaptation. In conclusion, our results indicate that the common and widespread H. radicata consists of locally adapted genotypes within its European range at a relatively small scale. Thus a large potential for gene flow by seeds and a high density of populations do not appear to be sufficient to prevent population differentiation by selection.

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, three from roadside verges and three from hayfields. Germination percentages and germination speed were higher for seeds from roadside verges than for seeds from hayfields, but were little affected by treatment. In contrast, seedling growth was much lower in the tall grass vegetation, than in the short grass and especially the bare soil treatment. Seedling sizes were generally similar for different populations and habitat types. Our results thus show that the two early steps in the establishment phase of plants may respond very differently to the micro-environment, and may have a different selection history. Insight into the ecology and evolution of life histories may require that germination and establishment are considered separately.

No abstract