It is well known that biodiversity positively affects ecosystem functioning, leading to enhanced ecosystem stability. However, this knowledge is mainly based on analyses using single ecosystem functions, while studies focusing on the stability of ecosystem multifunctionality (EMF) are rare. Taking advantage of a long‐term grassland biodiversity experiment, we studied the effect of plant diversity (1–60 species) on EMF over 5 y...

Soils are important for ecosystem functioning and service provisioning. Soil communities and their functions, in turn, are strongly promoted by plant diversity, and such positive effects strengthen with time. However, plant diversity effects on soil organic matter have mostly been investigated in the topsoil, and there are only very few long‐term studies. Thus, it remains unclear if plant diversity effects strengthen with time...

Aims We investigated the role of plants and their plant-derived carbon in shaping the microbial community that decomposes substrates and traced the return of nutrients from decomposition back to plant shoots in order to understand the importance of plants for ecosystem element cycling. Methods We performed a greenhouse experiment having plant communities with and without arbuscular mycorrhizal fungi (AMF) and ingrowth cores th...

The supply of soil respiration with recent photoassimilates is an important and fast pathway for respiratory loss of carbon (C). To date it is unknown how drought and land‐use change interactively influence the dynamics of recent C in soil‐respired CO 2 . In an in situ common‐garden experiment, we exposed soil‐vegetation monoliths from a managed and a nearby abandoned mountain grassland to an experimental drought. Based on two...

The catastrophic impact and unpredictability of the Indian Ocean Monsoon (IOM) over South Asia are evident from devastating floods, mudslides and droughts in one of the most densely populated regions of the globe. However, our understanding as to how the IOM has varied in the past, as well as its impact on local environments, remains limited. This is particularly the case for Sri Lanka, where erosional landscapes have limited...

Plant species richness ( PSR ) increases nutrient uptake which depletes bioavailable nutrient pools in soil. No such relationship between plant uptake and availability in soil was found for phosphorus (P). We explored PSR effects on P mobilisation [phosphatase activity ( PA )] in soil. PA increased with PSR . The positive PSR effect was not solely due to an increase in C org concentrations because PSR remained significant if r...

Little is known about the role of plant functional diversity for ecosystem‐level carbon (C) fluxes. To fill this knowledge gap, we translocated monoliths hosting communities with four and 16 sown species from a long‐term grassland biodiversity experiment (‘The Jena Experiment’) into a controlled environment facility for ecosystem research (Ecotron). This allowed quantifying the effects of plant diversity on ecosystem C fluxes...

Estimates of carbon leaching losses from different land use systems are few and their contribution to the net ecosystem carbon balance is uncertain. We investigated leaching of dissolved organic carbon (DOC), dissolved inorganic carbon (DIC), and dissolved methane (CH 4 ), at forests, grasslands, and croplands across Europe. Biogenic contributions to DIC were estimated by means of its δ 13 C signature. Leaching of biogenic DIC...

Increasing atmospheric CO 2 concentration and related climate change have stimulated much interest in the potential of soils to sequester carbon. In ‘The Jena Experiment’, a managed grassland experiment on a former agricultural field, we investigated the link between plant diversity and soil carbon storage. The biodiversity gradient ranged from one to 60 species belonging to four functional groups. Stratified soil samples were...

We studied the carbon flow of an allochthonous carbon source (sucrose) in a biofilm food web using stable isotope analysis and lipid biomarkers. Initial biofilms were grown for 2 weeks in a third order stream in Thuringia, Germany, and then incubated in replicate flow channels in climate‐controlled chambers. Either of two sucrose types, differing in their δ 13 C values, was added either immediately (2‐week‐old biofilm) or afte...