ALBERT

Description: This data collection contains species-specific aboveground plant biomass that was collected from the Trait Based Experiment in 2012. (Sown plant species, Weed plant biomass, the biomass of dead plant material, and the biomass of unidentified plant material) per plots collected in 2012 from a grassland trait diversity experiment (the Jena Trait Based Experiment). The data collection also contains the traits of the species measured in their monoculture. The experiment consists of 20 plant species that were assigned to one of three species pools: 1. Species that vary along a gradient of spatial leaf and root trait similarity, 2. Species that vary along a gradient of phenological trait similarity and 3. Species that vary along a gradient of both spatial and phenological similarity (see Ebeling et al. 2014). The experiment consists of 138 grassland plots 3 x 3 m in size that was established within the Jena Experiment, Germany, in 2011. Plots vary in plant species richness (1, 2, 4, or 8 species) and functional diversity (1, 2, 3, 4 functional diversity levels, where 1 indicates species are most similar and 4 being most dissimilar in functional traits). Plots were maintained by manual weeding in March, July and September. Biomass was harvested twice in 2012 (during peak standing biomass in late May and in late August) on all experimental plots. Plots were mown to the same height directly following biomass harvest. Plant biomass was harvested by clipping the vegetation at 3 cm above ground in two 0.2 x 0.5 m quadrats per plot. The harvested biomass was sorted into categories: individual species of the sown plant species, 'Weed' plant species (species not sown in a plot), detached 'Dead' plant material, and remaining plant material that could not be assigned to any category ('Rest'). All biomass was dried to constant weight (70°C, 〉= 48 h) and weighed. The data from individual quadrats were averaged. The traits measured are: Flowering initiation, Flowering cessation, specific leaf area (SLA), leaf dry matter content (LDMC), leaf area, maximum canopy height, specific root length (SRL), mean rooting depth (MRD), root mass density (RMD) and root length density (RLD). Flowering initiation and cessation were measured respectively as the week in which flowering was first observed and flowering senesce had completed throughout the plot. Leaf area, leaf fresh mass were measured on approximately five fully expanded leaves from different individuals. These leaves were dried at 65°C for over 48 hours and massed to calculate the specific leaf area (SLA, area per dry mass), and the leaf dry matter content (LDMC, dry mass per fresh mass). Maximum canopy height was measured during peak biomass in May by taking the average of five measurements along a transect. Root traits were measured by taking soil cores, 4 cm in diameter and 40 cm deep and sectioned by depth: 0-5, 5-10, 10-20, 20-30 and 30-40 cm. Roots were washed and roots 〈 2 mm in diameter were stored in 70 % ethanol. Root length was determined by scanning stained roots with neutral red and scanning roots using WinRhizo software. Root traits were only measured in species pool 1 and 2. Roots were then dried at 65°C for over 48 hours and massed to determine the specific root length (SRL, root length per mass), mean rooting depth (MRD, the average depth weighed by root mass per depth), root mass density (RMD, the average root mass per cubic cm volume) and root length density (RLD, root mass per root length).

Description: This data set contains plant species traits: Flowering initiation, Flowering cessation, specific leaf area (SLA), leaf dry matter content (LDMC), leaf area, maximum canopy height, specific root length (SRL), mean rooting depth (MRD), root mass density (RMD) and root length density (RLD). The traits were measured during the summer of 2012 on the plants grown in monoculture within a grassland trait diversity experiment (the Jena Trait Based Experiment). The experiment consists of 20 plant species that were assigned to one of three species pools: 1. Species that vary along a gradient of spatial leaf and root trait similarity, 2. Species that vary along a gradient of phenological trait similarity and 3. Species that vary along a gradient of both spatial and phenological similarity (see Ebeling et al. 2014). The plots were 3 x 3 m in size and established within the Jena Experiment, Germany, in 2011. Plots were maintained by manual weeding in March, July and September. Traits were measured during the summer of 2012. Flowering initiation and cessation were measured respectively as the week in which flowering was first observed and flowering senesce had completed throughout the plot. Leaf area, leaf fresh mass were measured on approximately five fully expanded leaves from different individuals. These leaves were dried at 65 C for over 48 hours and massed to calculate the specific leaf area (SLA, area per dry mass), and the leaf dry matter content (LDMC, dry mass per fresh mass). Maximum canopy height was measured during peak biomass in May by taking the average of five measurements along a transect. Root traits were measured by taking soil cores, 4 cm in diameter and 40 cm deep and sectioned by depth: 0-5, 5-10, 10-20, 20-30 and 30-40 cm. Roots were washed and roots 〈 2 mm in diameter were stored in 70 % ethanol. Root length was determined by scanning stained roots with neutral red and scanning roots using WinRhizo software. Root traits were only measured in species pool 1 and 2. Roots were then dried at 65 C for over 48 hours and massed to determine the specific root length (SRL, root length per mass), mean rooting depth (MRD, the average depth weighed by root mass per depth), root mass density (RMD, the average root mass per cubic cm volume) and root length density (RLD, root mass per root length).

Description: This data set contains environmental variables (imposed cumulative precipitation, measurements of radiation, air relative humidity and air temperature), measurements of soil water content, root water uptake estimated from soil moisture contents and community evapotranspiration derived from root water uptake as well as from weight changes, plant trait data (specific leaf area, leaf dry matter content, leaf water potential measured at predawn and midday, stomatal conductance, leaf greenness, height of species, aboveground biomass, species abundances, community leaf area index, vegetation and soil surface cover) and root trait data (biomass, length, diameter, surface area, tips, forks and crossings) from the 12 macrocosms used in the Jena-Ecotron Experiment in 2012. This experiment was conducted in the Montpellier European Ecotron (CNRS, France), an advanced controlled environment facility for ecosystem research, and aimed at understanding the impact of plant species richness (4 vs. 16 species) for ecosystem carbon and water fluxes. The soil monoliths used in this experiment contained plant communities originating from the long- term Jena Experiment (50°57.1' N, 11°37.5' E, 130 m above sea level; mean annual temperature 9.3°C, mean annual precipitation 587 mm) established in May 2002. Twelve plots were selected for the Jena-Ecotron study according to the following criteria: (1) the four functional groups grasses, legumes, small and tall herbs were present, (2) realized species numbers were close to sown species richness, and (3) plots were equally distributed across the experimental field site to account for different soil textures. Large monoliths (2 m² surface area, diameter of 1.6 m, 2 m depth with a weight of 7 to 8 tons) including intact soil and vegetation were excavated in December 2011 and placed in lysimeters. In March 2012, before the start of the vegetation growth, the lysimeters were transported and installed in the Macrocosms platform of the Montpellier European Ecotron. These data were used to investigate the characteristics of root water uptake profiles in grassland plant communities with different species richness (4-species and 16-species mixtures) and productivity to gain a deeper understanding of how plant species richness affects efficient use of available soil water.

Description: This data set contains aboveground plant biomass (Sown plant species, Weed plant biomass, the biomass of dead plant material, and the biomass of unidentified plant material) per plots collected in 2012 from a grassland trait diversity experiment (the Jena Trait Based Experiment). The experiment consists of 20 plant species that were assigned to one of three species pools: 1. Species that vary along a gradient of spatial leaf and root trait similarity, 2. Species that vary along a gradient of phenological trait similarity and 3. Species that vary along a gradient of both spatial and phenological similarity (see Ebeling et al. 2014). The experiment consists of 138 grassland plots 3 x 3 m in size that was established within the Jena Experiment, Germany, in 2011. Plots vary in plant species richness (1, 2, 4, or 8 species) and functional diversity (1, 2, 3, 4 functional diversity levels, where 1 indicates species are most similar and 4 being most dissimilar in functional traits). Plots were maintained by manual weeding in March, July and September. Biomass was harvested twice in 2012 (during peak standing biomass in late May and in late August) on all experimental plots. Plots were mown to the same height directly following biomass harvest. Plant biomass was harvested by clipping the vegetation at 3 cm above ground in two 0.2 x 0.5 m quadrats per plot. The location of these rectangles was assigned prior to each harvest by random selection of coordinates within the core area of the plots (i.e. the central 10 x 15 m). The positions of the rectangles within plots were identical for all plots. The harvested biomass was sorted into categories: individual species of the sown plant species, 'Weed' plant species (species not sown in a plot), detached 'Dead' plant material, and remaining plant material that could not be assigned to any category ('Rest'). All biomass was dried to constant weight (70°C, 〉= 48 h) and weighed. The data from individual quadrats were averaged.

Description: This dataset contains leaf water potential measured at predawn and midday of species in the Jena-Ecotron Experiment in 2012. This experiment was conducted in the Montpellier European Ecotron (CNRS, France), an advanced controlled environment facility for ecosystem research, and aimed at understanding the impact of plant species richness (4 vs. 16 species) for ecosystem carbon and water fluxes. The soil monoliths used in this experiment contained plant communities originating from the long- term Jena Experiment (50°57.1' N, 11°37.5' E, 130 m above sea level; mean annual temperature 9.3°C, mean annual precipitation 587 mm) established in May 2002. Twelve plots were selected for the Jena-Ecotron study according to the following criteria: (1) the four functional groups grasses, legumes, small and tall herbs were present, (2) realized species numbers were close to sown species richness, and (3) plots were equally distributed across the experimental field site to account for different soil textures. Large monoliths (2 m² surface area, diameter of 1.6 m, 2 m depth with a weight of 7 to 8 tons) including intact soil and vegetation were excavated in December 2011 and placed in lysimeters. In March 2012, before the start of the vegetation growth, the lysimeters were transported and installed in the Macrocosms platform of the Montpellier European Ecotron. Leaf water potential was measured with a pressure chamber (Pressure Chamber Instruments Model 600, PMS Instrument Company, Albany, Oregon, USA) at predawn (04:00 am - 06:00 am) and midday (01:30 pm - 04:00 pm) for the most abundant species on each plot from 17-19 July 2012. Two to three species were chosen in the 4-species mixtures, and five to eight species in the 16-species mixtures. Measurements were carried out on young, but fully expanded leaves from four individuals per species per plot. Stomatal conductance and leaf greenness were measured on three leaves from different individuals of all available species in each experimental unit. Values of leaf water potential of the individual measurements were averaged per species per plot.

Description: This dataset contains specific leaf area and leaf dry matter content in the Jena-Ecotron Experiment in 2012. This experiment was conducted in the Montpellier European Ecotron (CNRS, France), an advanced controlled environment facility for ecosystem research, and aimed at understanding the impact of plant species richness (4 vs. 16 species) for ecosystem carbon and water fluxes. The soil monoliths used in this experiment contained plant communities originating from the long- term Jena Experiment (50°57.1' N, 11°37.5' E, 130 m above sea level; mean annual temperature 9.3°C, mean annual precipitation 587 mm) established in May 2002. Twelve plots were selected for the Jena-Ecotron study according to the following criteria: (1) the four functional groups grasses, legumes, small and tall herbs were present, (2) realized species numbers were close to sown species richness, and (3) plots were equally distributed across the experimental field site to account for different soil textures. Large monoliths (2 m² surface area, diameter of 1.6 m, 2 m depth with a weight of 7 to 8 tons) including intact soil and vegetation were excavated in December 2011 and placed in lysimeters. In March 2012, before the start of the vegetation growth, the lysimeters were transported and installed in the Macrocosms platform of the Montpellier European Ecotron. To assess specific leaf area and leaf dry matter content, bulk samples of fully expanded leaves (1 to 7 leaves per plot and species) of the upper shoot part of all available plant species were collected during three days of the Ecotron campaign 2012 (combined with the measurements of stomatal conductance and leaf greenness). Bulk samples were put into moist paper in sealed plastic bags and stored in a cool box (refrigerator respectively) until sample processing in the laboratory. In the laboratory leaves were dried with tissue paper to remove any surface water and weighed immediately to determine their water-saturated fresh weight. The number of leaves per bulk sample was counted and leaf area was determined with a leaf area meter (LI-3000A, Licor, USA). Samples were overn-dried (70°C, 48h) and there dry mass was measured. Leaves of forb species were measured including petioles and rachis; in Galium mollugo a complete whirl was considered as a leaf. Leaf blades were measured as "leaves" in grass species., Instruments: LI-3000A, Licor, USA. Leaf dry matter content (= dry mass per unit fresh mass, LDMC; mg g-1) and specific leaf area (= leaf area per unit dry mass, SLA; mm2 mg-1) were calculated from these samples. Leaf samples were milled to a fine powder and analysed with an elemental analyzer (Flash EA 1112, Thermo Italy, Rhodano, Italy) to obtain leaf nitrogen (Nleaf; %) and carbon (Cleaf; %) concentrations.

Description: This dataset contains stomatal conductance, leaf greenness, and height of species in the Jena-Ecotron Experiment in 2012. This experiment was conducted in the Montpellier European Ecotron (CNRS, France), an advanced controlled environment facility for ecosystem research, and aimed at understanding the impact of plant species richness (4 vs. 16 species) for ecosystem carbon and water fluxes. The soil monoliths used in this experiment contained plant communities originating from the long- term Jena Experiment (50°57.1' N, 11°37.5' E, 130 m above sea level; mean annual temperature 9.3°C, mean annual precipitation 587 mm) established in May 2002. Twelve plots were selected for the Jena-Ecotron study according to the following criteria: (1) the four functional groups grasses, legumes, small and tall herbs were present, (2) realized species numbers were close to sown species richness, and (3) plots were equally distributed across the experimental field site to account for different soil textures. Large monoliths (2 m² surface area, diameter of 1.6 m, 2 m depth with a weight of 7 to 8 tons) including intact soil and vegetation were excavated in December 2011 and placed in lysimeters. In March 2012, before the start of the vegetation growth, the lysimeters were transported and installed in the Macrocosms platform of the Montpellier European Ecotron. Stomatal conductance (gs, mmol/m²/s) was measured with a portable leaf porometer (SC-1 Leaf porometer, Decagon Devices, Pullman, USA). Measurements were done in the auto mode using the first 30 s of stomatal conductance data to predict the final stomatal conductance under true steady state conditions. Leaf greenness (SPAD; unitless), an estimate of chlorophyll concentrations, was obtained by measuring the absorption of two different wavelength (650 nm and 940 nm) with a portable chlorophyll meter (SPAD-502; Konica-Minolta, Osaka, Japan). The growth height of three shoots (Ind h; cm) per species and unit was measured with a ruler. Values of stomatal conductance, leaf greenness and growth height of the individual measurements were averaged per species per plot.

Description: This dataset contains root traits (biomass, length, diameter, surface area, tips, forks and crossings) in the Jena-Ecotron Experiment in 2012. This experiment was conducted in the Montpellier European Ecotron (CNRS, France), an advanced controlled environment facility for ecosystem research, and aimed at understanding the impact of plant species richness (4 vs. 16 species) for ecosystem carbon and water fluxes. The soil monoliths used in this experiment contained plant communities originating from the long- term Jena Experiment (50°57.1' N, 11°37.5' E, 130 m above sea level; mean annual temperature 9.3°C, mean annual precipitation 587 mm) established in May 2002. Twelve plots were selected for the Jena-Ecotron study according to the following criteria: (1) the four functional groups grasses, legumes, small and tall herbs were present, (2) realized species numbers were close to sown species richness, and (3) plots were equally distributed across the experimental field site to account for different soil textures. Large monoliths (2 m² surface area, diameter of 1.6 m, 2 m depth with a weight of 7 to 8 tons) including intact soil and vegetation were excavated in December 2011 and placed in lysimeters. In March 2012, before the start of the vegetation growth, the lysimeters were transported and installed in the Macrocosms platform of the Montpellier European Ecotron. Three soil cores (diameter 3.5 cm) were sampled to 60 cm depth in each plot. Each core was divided into six layers (0-5, 5-10, 10-20, 20-30, 30-40 and 40-60 cm). The respective layers were pooled per plot, and washed with tap water over a sieve (mesh size 200 µm) to separate roots from soil. Cleaned roots were weighed and a subsample of the fresh roots (approx. 2 g) was stored in 70 % ethanol before it was dyed (with neutral red solution) and scanned (Scanner Optical STD4800 Regent Instruments Inc. with top light unit and an image resolution of 600 dpi). Root length density and root surface area were estimated with WinRhizo (Reg 2009c, Regents Instruments Inc.). The smooth off area of WinRhizo was set to 0.0001 and the length-width ratio to 3.0. Belowground biomass was estimated as described above but the samples were then dried at 65°C for three days.