Description of manganese deposits collected by R/V Nothwind during the 1963 expedition in the Laptev sea

The 400-km-wide, low gradient Laptev Sea continental shelf consists of flat terrace-like features at regular depth intervals from 10 to 40 m below present sea level. The five large submarine valleys traversing the shelf do not continuously grade seaward, but contain elongated, closed basins. These terraces and closed basins plus deltaic sediments associated with the submarine valleys quite possibly mark sea level Stillstands, and enable reconstruction of the paleogeography of the Laptev Sea shore line at five periods during post-Wisconsin (Holocene) time. Radiocarbon dates on the silty-clay to clayey-silt sediments from cores of the northeastern Laptev Sea indicate average sedimentation intensity of 2 to 15 mg/cm2/yr. The presence of manganese nodules and crusts in surface samples from less than 55 m depths and a general decrease in total foraminiferal abundances with depth in the cores suggest that the present deposition rate is less than when sea level was lower. The main components of the shelf deposits are near- shore sediments which were spread over the shelf as Holocene sea level fluctuated and marine currents distributed modern fine sediment. Rare silty-sand layers and the coarser nuclei of the manganese crusts and nodules indicate ice rafting. However, this mechanism is probably only locally important as a significant transporting agent.

(Table 1) Occurrence of selected planktonic foraminifers, other microfossils, and lithologic components at DSDP Hole 96-619

Site 619, located in the Pigmy Basin off the coast of Louisiana, penetrated the late Quaternary Ericson Zones X, Y, and Z. The penetrated section can be divided into four intervals. The lower interval (below 157 m sub-bottom) comprises 51 m of displaced sediments which probably originated from the Louisiana continental shelf. The upper three intervals (above 157 m) are dominated by pelagic/hemipelagic sedimentation associated with a closed basin. These are divided on the basis of planktonic foraminifers into Zones X, Y, and Z. These warm-cool water intervals are identified mainly by using the Globorotalia menardii complex (warm) and G. inflata (cool). The intervals correlate with published curves taken from piston core samples in the western Gulf of Mexico.

Grain size distribution and sea level changes in Gåsfjärden fjord

We analysed long-term variations in grain-size distribution in sediments from Gåsfjärden, a fjord-like inlet on the south-west Baltic Sea, and explored potential drivers of the recorded changes in sediment grain-size data. Over the last 5.4 thousand years (ka), the relative sea level decreased 17 m in the study region, caused by isostatic land uplift. As a consequence, Gåsfjärden has been transformed from an open coastal setting into a semi-closed inlet surrounded on the east by numerous small islands. To quantitatively estimate the morphological changes in Gåsfjärden over the last 5.4 ka and to further link the changes to our grain-size data, a digital elevation model (DEM)-based openness index was calculated. In the period between 5.4 and 4.4 ka BP, the inlet was characterised by the largest openness index. During this interval, the highest sand contents (~0.4 %) and silt/clay ratios (~0. 3) in the sediment sequence were recorded, indicating relatively high bottom water energy. After 4.4 ka BP, the average sand content was halved to ~0.2 % and the silt/clay ratios showed a significant decreasing trend over the last 4 ka. These changes are found to be associated with the gradual embayment of Gåsfjärden as represented in the openness index. The silt/clay ratios exhibited a delayed and slower change compared with the sand contents, which further suggest that finer particles are less sensitive to changes in hydrodynamic energy. Our DEM-based coastal openness index has proved to be a useful tool for interpreting the sedimentary grain-size record.

Collection of aboveground community and species-specific plant biomass from the Jena Experiment (time series since 2002).

This data set comprises time series of aboveground community plant biomass (Sown plant community, Weed plant community, Dead plant material, and Unidentified plant material; all measured in biomass as dry weight) and species-specific biomass from the sown species of several experiments at the field site of a large grassland biodiversity experiment (the Jena Experiment; see further details below). Aboveground community biomass was normally harvested twice a year just prior to mowing (during peak standing biomass twice a year, generally in May and August; in 2002 only once in September) on all experimental plots in the Jena Experiment. This was done by clipping the vegetation at 3 cm above ground in up to four rectangles of 0.2 x 0.5 m per large plot. The location of these rectangles was assigned by random selection of new coordinates every year within the core area of the plots. The positions of the rectangles within plots were identical for all plots. The harvested biomass was sorted into categories: individual species for the sown plant species, weed plant species (species not sown at the particular plot), detached dead plant material (i.e., dead plant material in the data file), and remaining plant material that could not be assigned to any category (i.e., unidentified plant material in the data file). All biomass was dried to constant weight (70°C, >= 48 h) and weighed. Sown plant community biomass was calculated as the sum of the biomass of the individual sown species. The data for individual samples and the mean over samples for the biomass measures on the community level are given. Overall, analyses of the community biomass data have identified species richness as well as functional group composition as important drivers of a positive biodiversity-productivity relationship. The following series of datasets are contained in this collection: 1. Plant biomass form the Main Experiment: In the Main Experiment, 82 grassland plots of 20 x 20 m were established from a pool of 60 species belonging to four functional groups (grasses, legumes, tall and small herbs). In May 2002, varying numbers of plant species from this species pool were sown into the plots to create a gradient of plant species richness (1, 2, 4, 8, 16 and 60 species) and functional richness (1, 2, 3, 4 functional groups). 2. Plant biomass from the Dominance Experiment: In the Dominance Experiment, 206 grassland plots of 3.5 x 3.5 m were established from a pool of 9 species that can be dominant in semi-natural grassland communities of the study region. In May 2002, varying numbers of plant species from this species pool were sown into the plots to create a gradient of plant species richness (1, 2, 3, 4, 6, and 9 species). 3. Plant biomass from the monoculture plots: In the monoculture plots the sown plant community contains only a single species per plot and this species is a different one for each plot. Which species has been sown in which plot is stated in the plot information table for monocultures (see further details below). The monoculture plots of 3.5 x 3.5 m were established for all of the 60 plant species of the Jena Experiment species pool with two replicates per species like the other experiments in May 2002. All plots were maintained by bi-annual weeding and mowing.