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Nitrogen (N) and phosphorus (P) limitation constrains the magnitude of terrestrial carbon uptake in response to elevated carbon dioxide and climate change. However, global maps of nutrient limitation are still lacking. Here we examined global N and P limitation using the ratio of site-averaged leaf N and P resorption efficiencies of the dominant species across 171 sites. We evaluated our predictions using a global database of N- and P-limitation experiments based on nutrient additions at 106 and 53 sites, respectively. Globally, we found a shift from relative P to N limitation for both higher latitudes and precipitation seasonality and lower mean annual temperature, temperature seasonality, mean annual precipitation and soil clay fraction. Excluding cropland, urban and glacial areas, we estimate that 18% of the natural terrestrial land area is significantly limited by N, whereas 43% is relatively P limited. The remaining 39% of the natural terrestrial land area could be co-limited by N and P or weakly limited by either nutrient alone. This work provides both a new framework for testing nutrient limitation and a benchmark of N and P limitation for models to constrain predictions of the terrestrial carbon sink.Spatial patterns in the phosphorus and nitrogen limitation in natural terrestrial ecosystems are reported from analysis of a global database of the resorption efficiency of nutrients by leaves.

Grazing has been associated with contrasting effects on soil carbon stocks at local scales, but accurate global assessments of its net impact are lacking. Here we conducted a meta-analysis of 1,473 soil carbon observations from grazing studies to quantify global changes in soil carbon stocks due to grazing practices. Our analysis shows that grazing has reduced soil carbon stocks at 1-m depth by 46 ± 13 PgC over the past 60 years. The interplay between grazing intensity and environmental factors explains global variations in soil carbon changes. Maps of optimal grazing intensity indicate that implementing grazing management on 21 million km 2 of grazing lands, mainly through decreasing grazing intensity on 75% of lands and increasing it on the rest could result in a potential uptake of 63 ± 18 PgC in vegetation and soils. These results highlight the potential of employing grazing as a climate mitigation strategy. Grazing has been shown to have diverse effects on soil carbon, with local variation. This study assesses carbon changes related to grazing globally and finds that, although grazing has reduced soil carbon stocks, managing intensity could increase carbon uptake in both soils and vegetation.

Urban greenspaces continue to grow with global urbanization. The global distribution and stock of soil organic carbon (SOC) in urban greenspaces remain largely undescribed and missing in global carbon (C) budgets. Here, we synthesize data of 420 observations from 257 cities in 52 countries to evaluate the global pattern of surface SOC density (0–20 cm depth) in urban greenspaces. Surface SOC density in urban greenspaces increases significantly at higher latitudes and decreases significantly with higher mean annual temperature, stronger temperature and precipitation seasonality, as well as lower urban greenness index. By mapping surface SOC density using a random forest model, we estimate an average SOC density of 55.2 (51.9–58.6) Mg C ha −1 and a SOC stock of 1.46 (1.37–1.54) Pg C in global urban greenspaces. Our findings present a comprehensive assessment of SOC in global urban greenspaces and provide a baseline for future urban soil C assessment under continuing urbanization. Using observed data, Guo et al. present a comprehensive assessment of soil organic carbon density and stock in global urban greenspaces. This study elucidates the global distribution of soil organic carbon in urban greenspaces and provides a baseline for future projection.

A poor understanding of the fraction of global plant biomass occurring belowground as roots limits our understanding of present and future ecosystem function and carbon pools. Here we create a database of root-mass fractions (RMFs), an index of plant below- versus aboveground biomass distributions, and generate quantitative, spatially explicit global maps of RMFs in trees, shrubs and grasses. Our analyses reveal large gradients in RMFs both across and within vegetation types that can be attributed to resource availability. High RMFs occur in cold and dry ecosystems, while low RMFs dominate in warm and wet regions. Across all vegetation types, the directional effect of temperature on RMFs depends on water availability, suggesting feedbacks between heat, water and nutrient supply. By integrating our RMF maps with existing aboveground plant biomass information, we estimate that in forests, shrublands and grasslands, respectively, 22%, 47% and 67% of plant biomass exists belowground, with a total global belowground fraction of 24% (20–28%), that is, 113 (90–135) Gt carbon. By documenting the environmental correlates of root biomass allocation, our results can inform model projections of global vegetation dynamics under current and future climate scenarios. The fraction of plant biomass in aboveground versus root tissues has implications for carbon storage and dynamics. Here the authors collate a dataset on root-mass fractions and use these data to explore large scale patterns of belowground plant biomass.

Vegetation impacts on ecosystem functioning are mediated by mycorrhizas, plant–fungal associations formed by most plant species. Ecosystems dominated by distinct mycorrhizal types differ strongly in their biogeochemistry. Quantitative analyses of mycorrhizal impacts on ecosystem functioning are hindered by the scarcity of information on mycorrhizal distributions. Here we present global, high-resolution maps of vegetation biomass distribution by dominant mycorrhizal associations. Arbuscular, ectomycorrhizal, and ericoid mycorrhizal vegetation store, respectively, 241 ± 15, 100 ± 17, and 7 ± 1.8 GT carbon in aboveground biomass, whereas non-mycorrhizal vegetation stores 29 ± 5.5 GT carbon. Soil carbon stocks in both topsoil and subsoil are positively related to the community-level biomass fraction of ectomycorrhizal plants, though the strength of this relationship varies across biomes. We show that human-induced transformations of Earth’s ecosystems have reduced ectomycorrhizal vegetation, with potential ramifications to terrestrial carbon stocks. Our work provides a benchmark for spatially explicit and globally quantitative assessments of mycorrhizal impacts on ecosystem functioning and biogeochemical cycling. Mycorrhizas—mutualistic relationships formed between fungi and most plant species—are functionally linked to soil carbon stocks. Here the authors map the global distribution of mycorrhizal plants and quantify links between mycorrhizal vegetation patterns and terrestrial carbon stocks.

Land ecosystems sequester on average about a quarter of anthropogenic CO2 emissions. It has been proposed that nitrogen (N) availability will exert an increasingly limiting effect on plants’ ability to store additional carbon (C) under rising CO2, but these mechanisms are not well understood. Here, we review findings from elevated CO2 experiments using a plant economics framework, highlighting how ecosystem responses to elevated CO2 may depend on the costs and benefits of plant interactions with mycorrhizal fungi and symbiotic N-fixing microbes. We found that N-acquisition efficiency is positively correlated with leaf-level photosynthetic capacity and plant growth, and negatively with soil C storage. Plants that associate with ectomycorrhizal fungi and N-fixers may acquire N at a lower cost than plants associated with arbuscular mycorrhizal fungi. However, the additional growth in ectomycorrhizal plants is partly offset by decreases in soil C pools via priming. Collectively, our results indicate that predictive models aimed at quantifying C cycle feedbacks to global change may be improved by treating N as a resource that can be acquired by plants in exchange for energy, with different costs depending on plant interactions with microbial symbionts.

Background and aims Through agriculture and industry, humans are increasing the deposition and availability of nitrogen (N) in ecosystems worldwide. Carbon (C) isotope tracers provide useful insights into soil C dynamics, as they allow to study soil C pools of different ages. We evaluated to what extent N enrichment affects soil C dynamics in experiments that applied C isotope tracers. Methods Using meta-analysis, we synthesized data from 35 published papers. We made a distinction between “new C” and “old C” stocks, i.e., soil C derived from plant C input since the start of the isotopic enrichment, or unlabeled, pre-existing soil C. Results Averaged across studies, N addition increased new soil C stocks (+30.3%), total soil C stocks (+6.1%) and soil C input proxies (+30.7%). Although N addition had no overall, average, effect on old soil C stocks and old soil C respiration, old soil C stocks increased with the amount of N added and respiration of old soil C declined. Nitrogen-induced effects on new soil C and soil C input both decreased with the amount of extraneous N added in control treatments. Conclusion Although our findings require additional confirmation from long-term field experiments, our analysis provides isotopic evidence that N addition stimulates soil C storage both by increasing soil C input and (at high N rates) by decreasing decomposition of old soil C. Furthermore, we demonstrate that the widely reported saturating response of plant growth to N enrichment also applies to new soil C storage.

Reforestation is a prominent climate change mitigation strategy, but available global maps of reforestation potential are widely criticized and highly variable, which limits their ability to provide robust estimates of both the locations and total area of opportunity. Here we develop global maps that address common critiques, build on a review of 89 reforestation maps created at multiple scales, and present eight reforestation scenarios with varying objectives, including providing ecosystem services, minimizing social conflicts, and delivering government policies. Across scenarios, we find up to 195 Mha (million hectares) are available (2225 TgCO 2 e (teragrams of carbon dioxide equivalent) per year total net mitigation potential), which is 71–92% smaller than previous estimates because of conservative modeling choices, incorporation of safeguards, and use of recent, high-resolution datasets. This area drops as low as 6 Mha (53 TgCO 2 e per year total net mitigation potential) if only statutorily protected areas are targeted. Few locations simultaneously achieve multiple objectives, suggesting that a mix of lands and restoration motivations will be needed to capitalize on the many potential benefits of reforestation. Reforestation is a key climate change mitigation strategy, but global maps of its potential are widely criticized. This study shows that addressing those critiques substantially refines estimates of the places with reforestation potential.

Despite worldwide prevalence, post-agricultural landscapes remain one of the least constrained human-induced land carbon sinks. To appraise their role in rebuilding the planet’s natural carbon stocks through ecosystem restoration, we need to better understand their spatial and temporal legacies.

Terrestrial ecosystems are subjected to multiple global changes simultaneously. Yet, how an increasing number of global changes impact the resistance of ecosystems to global change remains virtually unknown. Here we present a global synthesis including 14,000 observations from seven ecosystem services (functions and biodiversity), as well as data from a 15-year field experiment. We found that the resistance of multiple ecosystem services to global change declines with an increasing number of global change factors, particularly after long-term exposure to these factors. Biodiversity had a higher resistance to multiple global changes compared with ecosystem functions. Our work suggests that we need to consider the combined effects of multiple global changes on the magnitude and resistance of ecosystem services worldwide, as ecosystem responses will be enhanced by the number of environmental stressors and time of exposure.