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.

Phosphorus (P) limitation of aboveground plant production is usually assumed to occur in tropical regions but rarely elsewhere. Here we report that such P limitation is more widespread and much stronger than previously estimated. In our global meta-analysis, almost half (46.2%) of 652 P-addition field experiments reveal a significant P limitation on aboveground plant production. Globally, P additions increase aboveground plant production by 34.9% in natural terrestrial ecosystems, which is 7.0–15.9% higher than previously suggested. In croplands, by contrast, P additions increase aboveground plant production by only 13.9%, probably because of historical fertilizations. The magnitude of P limitation also differs among climate zones and regions, and is driven by climate, ecosystem properties, and fertilization regimes. In addition to confirming that P limitation is widespread in tropical regions, our study demonstrates that P limitation often occurs in other regions. This suggests that previous studies have underestimated the importance of altered P supply on aboveground plant production in natural terrestrial ecosystems.

Climate is predicted to change over the 21st century. However, little is known about how climate change can affect soil phosphorus (P) cycle and availability in global terrestrial ecosystems, where P is a key limiting nutrient. With a global database of Hedley P fractions and key‐associated physiochemical properties of 760 (seminatural) natural soils compiled from 96 published studies, this study evaluated how climate pattern affected soil P cycle and availability in global terrestrial ecosystems. Overall, soil available P, indexed by Hedley labile inorganic P fraction, significantly decreased with increasing mean annual temperature (MAT) and precipitation (MAP). Hypothesis‐oriented path model analysis suggests that MAT negatively affected soil available P mainly by decreasing soil organic P and primary mineral P and increasing soil sand content. MAP negatively affected soil available P both directly and indirectly through decreasing soil primary mineral P; however, these negative effects were offset by the positive effects of MAP on soil organic P and fine soil particles, resulting in a relatively minor total MAP effect on soil available P. As aridity degree was mainly determined by MAP, aridity also had a relatively minor total effect on soil available P. These global patterns generally hold true irrespective of soil depth (≤10 cm or >10 cm) or site aridity index (≤1.0 or >1.0), and were also true for the low‐sand (≤50%) soils. In contrast, available P of the high‐sand (>50%) soils was positively affected by MAT and aridity and negatively affected by MAP. Our results suggest that temperature and precipitation have contrasting effects on soil P availability and can interact with soil particle size to control soil P availability.

Significance: Elevated atmospheric N deposition threatens ecosystem health through eutrophication in terrestrial ecosystems, but little is known about consequences of N deposition in N-rich tropical ecosystems. We added several levels of N to an N-rich tropical forest and monitored plant growth dynamics, forest nutrient status, plant water use, and water losses from the ecosystem for a decade. We found that plants can acclimate and maintain nutrient balance by altering hydrological cycling. These results demonstrate that while elevated N deposition to already N-rich tropical forests may have minor effects on forest growth, it can exert a detectable influence on hydrological dynamics. Reduced runoff may threaten water supply in rapidly developing tropical regions.

The dynamics of phosphorus (P) in the environment is important for regulating nutrient cycles in natural and managed ecosystems and an integral part in assessing biological resilience against environmental change. Organic P (P_o) compounds play key roles in biological and ecosystems function in the terrestrial environment being critical to cell function, growth and reproduction.

Soil represents the largest phosphorus (P) stock in terrestrial ecosystems. Determining the amount of soil P is a critical first step in identifying sites where ecosystem functioning is potentially limited by soil P availability. However, global patterns and predictors of soil total P concentration remain poorly understood. To address this knowledge gap, we constructed a database of total P concentration of 5275 globally distributed (semi-)natural soils from 761 published studies. We quantified the relative importance of 13 soil-forming variables in predicting soil total P concentration and then made further predictions at the global scale using a random forest approach. Soil total P concentration varied significantly among parent material types, soil orders, biomes, and continents and ranged widely from 1.4 to 9630.0 (median 430.0 and mean 570.0) mg kg⁻¹ across the globe. About two-thirds (65 %) of the global variation was accounted for by the 13 variables that we selected, among which soil organic carbon concentration, parent material, mean annual temperature, and soil sand content were the most important ones. While predicted soil total P concentrations increased significantly with latitude, they varied largely among regions with similar latitudes due to regional differences in parent material, topography, and/or climate conditions. Soil P stocks (excluding Antarctica) were estimated to be 26.8 ± 3.1 (mean ± standard deviation) Pg and 62.2 ± 8.9 Pg (1 Pg = 1 × 10¹⁵ g) in the topsoil (0–30 cm) and subsoil (30–100 cm), respectively. Our global map of soil total P concentration as well as the underlying drivers of soil total P concentration can be used to constraint Earth system models that represent the P cycle and to inform quantification of global soil P availability. Raw datasets and global maps generated in this study are available at https://doi.org/10.6084/m9.figshare.14583375 (He et al., 2021).