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Tropical forests store large amounts of biomass despite they generally grow in nutrient-poor soils, suggesting that the role of soil characteristics in the structure and dynamics of tropical forests is complex. We used data for >34 000 trees from several permanent plots in French Guiana to investigate if soil characteristics could predict the structure (tree diameter, density and aboveground biomass), and dynamics (growth, mortality, aboveground wood productivity) of nutrient-poor tropical forests. Most variables did not covary with site-level changes in soil nutrient content, indicating that nutrient-cycling mechanisms other than the direct absorption from soil (e.g. the nutrient uptake from litter, the resorption, or the storage of nutrients in the biomass), may strongly control forest structure and dynamics. Ecosystem-level adaptations to low soil nutrient availability and long-term low levels of disturbance may help to account for the lower productivity and higher accumulation of biomass in nutrient-poor forests compared to nutrient-richer forests.

International audience; Frequency and intensity of heat waves and drought events are expected to increase in Europe due to climate change. European beech (Fagus sylvatica L.) is one of the most important native tree species in Europe. Beech populations originating throughout its native range were selected for common-garden experiments with the aim to determine whether there are functional variations in drought stress responses among different populations. One-year old seedlings from four to seven beech populations were grown and drought treated in a greenhouse, replicating the experiment at two contrasting sites, in Italy (Mediterranean mountains) and Germany (Central Europe). Experimental findings indicated that: (1) drought (water stress) mainly affected gas exchange describing a critical threshold of drought response between 30 and 26% SWA for photosynthetic rate and C-i/C-a, respectively; (2) the C-i to C-a ratio increased substantially with severe water stress suggesting a stable instantaneous water use efficiency and an efficient regulation capacity of water balance achieved by a tight stomatal control; (3) there was a different response to water stress among the considered beech populations, differently combining traits, although there was not a well-defined variability in drought tolerance. A combined analysis of functional and structural traits for detecting stress signals in beech seedlings is suggested to assess plant performance under limiting moisture conditions and, consequently, to estimate evolutionary potential of beech under a changing environmental scenario.

We studied the growth and photosynthetic capacity of Berberis darwinii shrub growing under different light conditions in their native area of Argentina to test if plant physiology differs from invaded area (using studies carried out in New Zealand). In its native range B. darwinii grows under different light conditions by adjusting shoot and leaf morphology and physiology. Plants of B. darwinii growing under the same light environments show similar physiology in native and invasive ranges. Therefore, intra-specific variations of the functional traits in native area do not condition successful invasiveness., Invasive species' success may depend on ecophysiological attributes present in their native area or those derived from changes that took place in the invaded environment. We studied the growth and photosynthetic capacity of Berberis darwinii shrubs growing under different light conditions (gap, forest edge and below the canopy) in their native area of Patagonia, Argentina. Leaf photosynthesis results determined in the native area were discussed in relation to information provided by studies carried out under the same light conditions in an invaded area in New Zealand. Shoot elongation, leaf production, stem and leaf biomass per shoot, and specific leaf area (SLA, cm2 g−1) were determined in five adult plants, randomly selected in each of the three light conditions at two forest sites. Net photosynthesis as a function of PPFD (photosynthetic photon flux density), stomatal conductance (gs), maximum light-saturated photosynthesis rate (Pmax), Pmass (on mass bases) and water-use efficiency (WUEi) were determined in plants of one site. We predicted that functional traits would differ between populations of native and invasive ranges. In their native area, plants growing under the canopy produced the longest shoots and had the lowest values for shoot emergence and foliar biomass per shoot, while their SLA was higher than gap and forest edge plants. Leaf number and stem biomass per shoot were independent of light differences. Leaves of gap plants showed higher Pmax, Pmass and gs but lower WUEi than plants growing at the forest edge. In its native range B. darwinii grows under different light conditions by adjusting shoot and leaf morphology and physiology. Plants of B. darwinii growing under the same light conditions show similar physiology in native and invasive ranges. This means that for B. darwinii, intra-specific variation of the functional traits studied here does not condition successful spread in new areas.

One challenge of evolutionary ecology is to predict the rate and mechanisms of population adaptation to environmental variations. The variations in most life-history traits are shaped both by individual genotypic and environmental variation. Forest trees exhibit high levels of genetic diversity, large population sizes, and gene flow, and they also show a high level of plasticity for life-history traits. We developed a new Physio-Demo-Genetics model (denoted PDG) coupling (1) a physiological module simulating individual tree responses to the environment; (2) a demographic module simulating tree survival, reproduction and pollen and seed dispersal; and (3) a quantitative genetics module controlling the heritability of key life history traits. We used this model to investigate the plastic and genetic components of the variations of the timing of budburst along an elevational gradient of Fagus sylvatica (the European beech). We used a repeated five years climatic sequence to show that five generations of natural selection were sufficient to develop non-monotonic genetic differentiation in the timing of budburst along the local climatic gradient but also that plastic variation among different elevations and years was higher than genetic variation. PDG complements theoretical models and provides testable predictions to understand the adaptive potential of tree populations