Total organic carbon, delta13C, biomarker, diatom distributions in sediment core JM11-FI-19PC

In the light of rapidly diminishing sea ice cover in the Arctic during the present atmospheric warming, it is imperative to study the distribution of sea ice in the past in relation to rapid climate change. Here we focus on glacial millennial scale climatic events (Dansgaard/Oeschger events) using the new sea ice proxy IP25 in combination with phytoplankton proxy data and quantification of diatom species in a record from the SE Norwegian Sea. We demonstrate that expansion and retreat of sea ice varied consistently in pace with the rapid climate changes 90 ka to present, and with this present the first IP25 sea ice proxy record resolving the D/O cyclicity going back in time into Marine Isotope Stage 5a. Sea ice retreated abruptly at the start of warm interstadials, but spread rapidly during the cooling phase of the interstadials and became near-perennial and perennial during cold stadials and Heinrich events, respectively. Low salinity surface water and the sea ice edge spread to the Greenland-Scotland Ridge, and during the largest Heinrich events, probably far into the Atlantic Ocean.

Mineral nitrogen from KCl extractions of soil from the Jena Experiment (Main Experiment up to 30cm depth, year 2003)

As an estimate of plant-available N, this data set contains measurements of inorganic nitrogen (NO3-N and NH4-N, the sum of which is termed mineral N or Nmin) determined by extraction with 1 M KCl solution of soil samples from the main experiment plots of a large grassland biodiversity experiment (the Jena Experiment; see further details below). 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). Plots were maintained by bi-annual weeding and mowing. Soil sampling and analysis: Five soil cores (diameter 0.01 m) were taken at a depth of 0 to 0.15 m and 0.15 to 0.3 m of the mineral soil from each of the experimental plots in March, June, and October 2003. Samples of the soil cores per plot were pooled during each sampling campaign. NO3-N and NH4-N concentrations were determined by extraction of soil samples with 1 M KCl solution and were measured in the soil extract with a Continuous Flow Analyzer (CFA, Skalar, Breda, Netherlands).