Plant traits-the morphological, anatomical, physiological, biochemical and phenological characteristics of plants-determine how plants respond to environmental factors, affect other trophic levels, and influence ecosystem properties and their benefits and detriments to people. Plant trait data thus represent the basis for a vast area of research spanning from evolutionary biology, community and functional ecology, to biodiversity conservation, ecosystem and landscape management, restoration, biogeography and earth system modelling. Since its foundation in 2007, the TRY database of plant traits has grown continuously. It now provides unprecedented data coverage under an open access data policy and is the main plant trait database used by the research community worldwide. Increasingly, the TRY database also supports new frontiers of trait-based plant research, including the identification of data gaps and the subsequent mobilization or measurement of new data. To support this development, in this article we evaluate the extent of the trait data compiled in TRY and analyse emerging patterns of data coverage and representativeness. Best species coverage is achieved for categorical traits-almost complete coverage for 'plant growth form'. However, most traits relevant for ecology and vegetation modelling are characterized by continuous intraspecific variation and trait-environmental relationships. These traits have to be measured on individual plants in their respective environment. Despite unprecedented data coverage, we observe a humbling lack of completeness and representativeness of these continuous traits in many aspects.We, therefore, conclude that reducing data gaps and biases in the TRY database remains a key challenge and requires a coordinated approach to data mobilization and trait measurements. This can only be achieved in collaboration with other initiatives. Geosphere-Biosphere Program (IGBP) and DIVERSITAS, the TRY database (TRY-not an acronym, rather a statement of sentiment; https ://www.try-db.org; Kattge et al., 2011) was proposed with the explicit assignment to improve the availability and accessibility of plant trait data for ecology and earth system sciences. The Max Planck Institute for Biogeochemistry (MPI-BGC) offered to host the database and the different groups joined forces for this community-driven program. Two factors were key to the success of TRY: the support and trust of leaders in the field of functional plant ecology submitting large databases and the long-term funding by the Max Planck Society, the MPI-BGC and the German Centre for Integrative Biodiversity Research (iDiv) Halle-Jena-Leipzig, which has enabled the continuous development of the TRY database.

Seed dispersal by frugivores plays a key role in structuring and maintaining tree diversity in forests. However, little is known about how the spatial legacy of seed dispersal and early recruitment shapes spatial patterns and the spatial interaction network of plant species in mature forest communities. We analysed two fully mapped mixed Pine–Oak forest communities using spatial point pattern analysis to determine (a) the detailed structure of the intraspecific spatial patterns of saplings and adults, (b) the intra‐ and interspecific spatial interaction of saplings, adults and saplings relative to adults, (c) the spatial patterns of species richness at the community level and (d) whether seed dispersal mechanisms affect the plant–plant interaction networks and the ratio of adult to sapling neighbourhood densities used as surrogate for spatial self‐thinning. The intraspecific spatial patterns of saplings and adults showed in general complex nested cluster structures that were similar for sapling and adult stages, despite substantial self‐thinning in some dry‐fruited species. The spatial network of saplings was characterized by positive spatial interactions. Adults of several tree species facilitated saplings in their proximity; however, adults of dry‐fruited species, but not those of fleshy‐fruited ones, lost almost all positive interactions that occurred at the sapling stage. Besides, interaction strength between adults was positive and often significantly stronger if both species were fleshy‐fruited. At the community level, the forests were structured into multispecies clumps across all life stages. Synthesis. Our analyses highlight the importance of the spatial legacy of seed dispersal and early recruitment in the assembly of plant communities. Particularly, animal seed dispersal can lead to multispecies clusters and positive spatial associations across life stages in Mediterranean forests, with surprisingly little signatures of negative interactions. Our analysis suggests that changes of the spatial structure across plant life stages are driven by seed dispersal mechanisms and subsequent spatial self‐thinning, generating a spatial footprint at the sapling stage that conditions the long‐term interactions between adult plants. Combining spatial point pattern analysis with network analysis and species traits is a promising way to disentangle the processes underlying observed patterns of local diversity.

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Questions: The assembly of plant communities depends strongly on mechanisms that determine the recruitment of different plant species. Studying recruitment using a trait-based approach may help in the search for general or dominant mechanisms involved in this process. Here, we try to disentangle what traits of saplings and established (canopy) plants can be considered as functional for recruitment, and whether the complementarity of these functional traits may be a driver of the plant community assembly. Location: Regional. Two pine-oak forest communities in Sierra Sur de Jaén and one in Sierra de Segura, southeast of the Iberian peninsula. Methods: In each forest community, we established three 50 m × 50 m plots, where we identified the saplings of each species recruiting under the canopy of each species or in open interspaces. The study focuses on 37 woody species. Measures of 18 traits were conducted for 30 saplings and 10 adults of each species. Results: Seed mass and the ratio height:basal diameter of saplings were positively associated with species abundance in the sapling bank under vegetation, while abundance in the sapling bank in open interspaces was only related to the type of mycorrhizal association. On the other hand, some traits of adult plants (leaf mass per unit area [LMA], seed dispersal mechanism, leaf habit and branch density) favour the recruitment of other species in their close proximity. However, we found only circumstantial evidence of canopy/recruit trait complementarity affecting recruitment. Conclusions: Our results suggest that the assembly of canopy-recruit interactions is primarily driven by the filtering effect of canopy species on recruitment, through traits that affect both seed arrival and soil properties. Species abundance in the sapling bank was related to resource acquisition traits. We did not find any clear evidence supporting that trait complementarity is involved in the interaction between canopy and recruit species.

The analysis of the spatial phylogenetic and phenotypic structure of plant communities can provide insight into the underlying processes and interactions governing their assembly, and how these may change during plant ontogeny. We used point pattern analysis to find out if saplings and adult plants are surrounded by phylogenetically and phenotypically more similar or more dissimilar neighbours than expected by chance, and whether these associations change from the sapling to the adult stage. To this end, we combined information on the phylogenetic structure and eight phenotypic traits of 15 woody plant species in two Mediterranean mixed forests of southeastern Spain. At the community level, we found that the sapling bank at both sites did not show phylogenetic or phenotypic spatial patterns, but adults showed phylogenetic clustering (i.e. heterospecific neighbours were more similar than expected). At the species level, we found frequently repulsive patterns in the sapling bank of less abundant species (i.e. heterospecific sapling or adult neighbours were more dissimilar than expected) in both, phylogenetic and phenotypic analyses. For the adult stage, we found phylogenetic attraction (i.e. more similar neighbours) in just one species and phenotypic clustering in four species. The processes driving the assembly of the communities of saplings and adults leave detectable signals in the spatial phylogenetic and phenotypic structure of our two forest communities. Our findings reinforce the existence of ontogenetic shifts in the mechanisms involved in plant community assembly. Facilitation between phylogenetically distant and phenotypically divergent species favours the recruitment of less abundant species. However, processes acting later in the ontogeny ameliorate the competition between close relatives and determine the spatial structure of adult plants. Nevertheless, the role of phenotype in shaping the interactions between adult plants was context‐ and trait‐dependent. The use of spatial point pattern analysis allowed a nuanced interpretation of the phylogenetic and phenotypic structures of plant communities.