Land-use change (LUC) is a major driving factor for the balance of soil organic carbon (SOC) stocks and the global carbon cycle. The temporal dynamic of SOC after LUC is especially important in temperate systems with a long reaction time. On the basis of 95 compiled studies covering 322 sites in the temperate zone, carbon response functions (CRFs) were derived to model the temporal dynamic of SOC after five different LUC types (mean soil depth of 30 AE 6 cm). Grassland establishment caused a long lasting carbon sink with a relative stock change of 128 AE 23% and afforestation on former cropland a sink of 116 AE 54%, 100 years after LUC (mean AE 95% confidence interval). No new equilibrium was reached within 120 years. In contrast, there was no SOC sink following afforestation of grasslands and 75% of all observations showed SOC losses, even after 100 years. Only in the forest floor, there was carbon accumulation of 0.38 AE 0.04 Mg ha À1 yr À1 in afforestations adding up to 38 AE 4 Mg ha À1 labile carbon after 100 years. Carbon loss after deforestation (À32 AE 20%) and grassland conversion to cropland (À36 AE 5%), was rapid with a new SOC equilibrium being reached after 23 and 17 years, respectively. The change rate of SOC increased with temperature and precipitation but decreased with soil depth and clay content. Subsoil SOC changes followed the trend of the topsoil SOC changes but were smaller (25 AE 5% of the total SOC changes) and with a high uncertainty due to a limited number of datasets. As a simple and robust model approach, the developed CRFs provide an easily applicable tool to estimate SOC stock changes after LUC to improve greenhouse gas reporting in the framework of UNFCCC.
The importance of biodiversity in supporting ecosystem functioning is generally well accepted. However, most evidence comes from small-scale studies, and scaling-up patterns of biodiversity-ecosystem functioning (B-EF) remains challenging, in part because the importance of environmental factors in shaping B-EF relations is poorly understood. Using a forest research platform in which 26 ecosystem functions were measured along gradients of tree species richness in six regions across Europe, we investigated the extent and the potential drivers of context dependency of B-EF relations. Despite considerable variation in species richness effects across the continent, we found a tendency for stronger B-EF relations in drier climates as well as in areas with longer growing seasons and more functionally diverse tree species. The importance of water availability in driving context dependency suggests that as water limitation increases under climate change, biodiversity may become even more important to support high levels of functioning in European forests.
Explaining the large-scale diversity of soil organisms that drive biogeochemical processes-and their responses to environmental change-is critical. However, identifying consistent drivers of belowground diversity and abundance for some soil organisms at large spatial scales remains problematic. Here we investigate a major guild, the ectomycorrhizal fungi, across European forests at a spatial scale and resolution that is-to our knowledge-unprecedented, to explore key biotic and abiotic predictors of ectomycorrhizal diversity and to identify dominant responses and thresholds for change across complex environmental gradients. We show the effect of 38 host, environment, climate and geographical variables on ectomycorrhizal diversity, and define thresholds of community change for key variables. We quantify host specificity and reveal plasticity in functional traits involved in soil foraging across gradients. We conclude that environmental and host factors explain most of the variation in ectomycorrhizal diversity, that the environmental thresholds used as major ecosystem assessment tools need adjustment and that the importance of belowground specificity and plasticity has previously been underappreciated.
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