Deglaciation chronology,sea-level changes and environmental changes from Holocene lake sediments of Germania Havn Sø, Sabine Ø, northeast Greenland

Germania Havn Sø is located at the outermost coast of northeastern Greenland. According to radiocarbon dating, the lake basin was deglaciated in the early Holocene, around 11,000 cal yr BP. At that time the lake was a marine bay, but the lake was isolated soon after deglaciation at ~ 10,600 cal yr BP. The marine fauna was species-poor, indicating harsh conditions with a high sedimentation rate and lowered salinity due to glacial meltwater supply. The pioneer vegetation around the lake was dominated by mosses and herbs. Deposition of relatively coarse sediments during the early Holocene indicates erosion of the newly deglaciated terrain. Remains of the first woody plant (Salix herbacea) appear at 7600 cal yr BP and remains of other woody plants (Salix arctica, Dryas octopetala, Cassiope tetragona and Empetrum nigrum) appear around one millennium later. Declining concentrations of D. octopetala and the caddis fly Apatania zonella in the late Holocene probably imply falling summer temperatures. Only moderate changes in the granulometric and geochemical record during the Holocene indicate relatively stable environmental settings in the lake, which can probably be explained by its location at the outer coast and the buffering effect of the neighboring ocean.     

Surface Charge Concentrations on Silica in Different 1.0 M Metal-Chloride Background Electrolytes and Implications for Dissolution Rates

The empirical rate laws formulated to describe the dissolution rates of oxide minerals include the surface charge concentration that results from the protonation and deprotonation of surface functional groups. Previous experiments on quartz and silica have shown that dissolution rates vary as a function of different background electrolyte solutions, however, such experiments are often conducted at elevated temperatures where it is difficult to estimate surface charge along with the dissolution rates. In the present study we measuresurface charge concentrations for silica in different electrolyte solutions at 298 K in order to quantify the extent to which the different counterions could affect the dissolution rates through their influence on the surface charge concentrations. The experimental solutions in the electrolyte series: LiCl, NaCl, KCl, RbCl, CaCl₂, SrCl₂ and BaCl₂ were prepared to maintain a constant metal concentration of 1.0 M. For the alkali-metal chlorides, the surface charge concentrations correlate with the size of the hydrated alkali metal, consistent with the idea that these counterions affect charge via outer-sphere coordination that shield proton surface complexes from one another. The reactivity trend for alkaline-earth cations is less clear, but the data demonstrate distinct differences in the acid-base propertiesof the silica surface in these different electrolytes. We then discuss how these trends are manifested in the rate equations used to interpret dissolution experiments.