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.

A substantial body of evidence has demonstrated that biodiversity stabilizes ecosystem functioning over time in grassland ecosystems. However, the relative importance of different facets of biodiversity underlying the diversity-stability relationship remains unclear. Here we use data from 39 grassland biodiversity experiments and structural equation modelling to investigate the roles of species richness, phylogenetic diversity and both the diversity and community-weighted mean of functional traits representing the 'fast-slow' leaf economics spectrum in driving the diversity-stability relationship. We found that high species richness and phylogenetic diversity stabilize biomass production via enhanced asynchrony in the performance of co-occurring species. Contrary to expectations, low phylogenetic diversity enhances ecosystem stability directly, albeit weakly. While the diversity of fast-slow functional traits has a weak effect on ecosystem stability, communities dominated by slow species enhance ecosystem stability by increasing mean biomass production relative to the standard deviation of biomass over time. Our in-depth, integrative assessment of factors influencing the diversity-stability relationship demonstrates a more multicausal relationship than has been previously acknowledged.

Lysenko 91,92 | Armin Macanović 93 | Parastoo Mahdavi 94 | Peter Manning 35 | Corrado Marcenò 13 | Vassiliy Martynenko 95 | Maurizio Mencuccini 96 | Vanessa Minden 97 | Jesper Erenskjold Moeslund 54 | Marco Moretti 98 | Jonas V. Müller 99 | Abstract Aims: Vegetation-plot records provide information on the presence and cover or abundance of plants co-occurring in the same community. Vegetation-plot data are spread across research groups, environmental agencies and biodiversity research centers and, thus, are rarely accessible at continental or global scales. Here we present the sPlot database, which collates vegetation plots worldwide to allow for the exploration of global patterns in taxonomic, functional and phylogenetic diversity at the plant community level.Results: sPlot version 2.1 contains records from 1,121,244 vegetation plots, which comprise 23,586,216 records of plant species and their relative cover or abundance in plots collected worldwide between 1885 and 2015. We complemented the information for each plot by retrieving climate and soil conditions and the biogeographic context (e.g., biomes) from external sources, and by calculating community-weighted means and variances of traits using gap-filled data from the global plant trait database TRY. Moreover, we created a phylogenetic tree for 50,167 out of the 54,519 species identified in the plots. We present the first maps of global patterns of community richness and community-weighted means of key traits. Conclusions: The availability of vegetation plot data in sPlot offers new avenues for vegetation analysis at the global scale. K E Y W O R D S biodiversity, community ecology, ecoinformatics, functional diversity, global scale, macroecology, phylogenetic diversity, plot database, sPlot, taxonomic diversity, vascular plant, vegetation relevé 166 |

Our ability to understand and predict the response of ecosystems to a changing environment depends on quantifying vegetation functional diversity. However, representing this diversity at the global scale is challenging. Typically, in Earth system models, characterization of plant diversity has been limited to grouping related species into plant functional types (PFTs), with all trait variation in a PFT collapsed into a single mean value that is applied globally. Using the largest global plant trait database and state of the art Bayesian modeling, we created fine-grained global maps of plant trait distributions that can be applied to Earth system models. Focusing on a set of plant traits closely coupled to photosynthesis and foliar respiration-specific leaf area (SLA) and dry mass-based concentrations of leaf nitrogen (Nm) and phosphorus (Pm), we characterize how traits vary within and among over 50,000 ∼50 × 50-km cells across the entire vegetated land surface. We do this in several ways-without defining the PFT of each grid cell and using 4 or 14 PFTs; each model's predictions are evaluated against out-of-sample data. This endeavor advances prior trait mapping by generating global maps that preserve variability across scales by using modern Bayesian spatial statistical modeling in combination with a database over three times larger than that in previous analyses. Our maps reveal that the most diverse grid cells possess trait variability close to the range of global PFT means.odeling global climate and the carbon cycle with Earth system models (ESMs) requires maps of plant traits that play key roles in leaf-and ecosystem-level metabolic processes (1-4). Multiple traits are critical to both photosynthesis and respiration, foremost leaf nitrogen concentration (Nm ) and specific leaf area (SLA) (5-7). More recently, variation in leaf phosphorus concentration (Pm ) has also been linked to variation in photosynthesis and foliar respiration (7-12). Estimating detailed global geographic patterns of these traits and corresponding trait-environment relationships has been hampered by limited measurements (13), but recent improvements in data coverage (14) allow for greater detail in spatial estimates of these key traits.Previous work has extrapolated trait measurements across continental or larger regions through three methodologies: (i) grouping measurements of individuals into larger categories that share a set of properties [a working definition of plant functional types (PFTs)] (4, 15), (ii) exploiting trait-environment relationships (e.g., leaf Nm and mean annual temperature) (1,(16)(17)(18)(19)(20), or (iii) restricting the analysis to species whose presence has been widely estimated on the ground (21-24). Each of these methods has limitations-for example, trait-environment relationships do not well explain observed trait spatial patterns (1, 25), while species-based approaches limit the scope of extrapolation to only areas with well-measured species abundance. More critically, the first two global methodologies emp...

Summary1. Biotic resistance, the ability of species in a community to limit invasion, is central to our understanding of how communities at risk of invasion assemble after disturbances, but it has yet to translate into guiding principles for the restoration of invasion-resistant plant communities. We combined experimental, functional, and modelling approaches to investigate processes of community assembly contributing to biotic resistance to an introduced lineage of Phragmites australis, a model invasive species in North America. We hypothesized that (i) functional group identity would be a good predictor of biotic resistance to P. australis, while species identity effect would be redundant within functional group (ii) mixtures of species would be more invasion resistant than monocultures. 2. We classified 36 resident wetland plants into four functional groups based on eight functional traits. We conducted two competition experiments based on the additive competition design with P. australis and monocultures or mixtures of wetland plants. As an indicator of biotic resistance, we calculated a relative competition index (RCI avg ) based on the average performance of P. australis in competition treatment compared with control. To explain diversity effect further, we partitioned it into selection effect and complementarity effect and tested several diversity-interaction models. 3. In monoculture treatments, RCI avg of wetland plants was significantly different among functional groups, but not within each functional group. We found the highest RCI avg for fast-growing annuals, suggesting priority effect. 4. RCI avg of wetland plants was significantly greater in mixture than in monoculture mainly due to complementarity-diversity effect among functional groups. In diversity-interaction models, species interaction patterns in mixtures were described best by interactions between functional groups when fitted to RCI avg or biomass, implying niche partitioning. 5. Synthesis. Functional group identity and diversity of resident plant communities are good indicators of biotic resistance to invasion by introduced Phragmites australis, suggesting niche preemption (priority effect) and niche partitioning (diversity effect) as underlying mechanisms. Guiding principles to understand and/or manage biological invasion could emerge from advances in community theory and the use of a functional framework. Targeting widely distributed invasive plants in different contexts and scaling up to field situations will facilitate generalization.

Plant functional traits can predict community assembly and ecosystem functioning and are thus widely used in global models of vegetation dynamics and land–climate feedbacks. Still, we lack a global understanding of how land and climate affect plant traits. A previous global analysis of six traits observed two main axes of variation: (1) size variation at the organ and plant level and (2) leaf economics balancing leaf persistence against plant growth potential. The orthogonality of these two axes suggests they are differently influenced by environmental drivers. We find that these axes persist in a global dataset of 17 traits across more than 20,000 species. We find a dominant joint effect of climate and soil on trait variation. Additional independent climate effects are also observed across most traits, whereas independent soil effects are almost exclusively observed for economics traits. Variation in size traits correlates well with a latitudinal gradient related to water or energy limitation. In contrast, variation in economics traits is better explained by interactions of climate with soil fertility. These findings have the potential to improve our understanding of biodiversity patterns and our predictions of climate change impacts on biogeochemical cycles.

This paper introduces a modular processing chain to derive global highresolution maps of leaf traits. In particular, we present global maps at 500 m resolution of specific leaf area, leaf dry matter content, leaf nitrogen and

Ecological theory is built on trade-offs where trait differences among species evolved as adaptations to different environments. Trade-offs are often assumed to be bidirectional, where opposite ends of a gradient in trait values confer advantages in different environments. However, unidirectional benefits could be widespread if extreme trait values confer advantages at one end of an environmental gradient, whereas a wide range of trait values are equally beneficial at the