Chemical stratigraphy of recent sediments from a depth gradient in a meromictic lake, Nordbytjernet, SE Norway, in relation to variable external loading and sedimentary fluxes

Abstract

Cores of recent sediments were sampled along a depth gradient in a 23 m deep kettle lake with stagnant deep waters containing exceptionally high concentrations of dissolved iron and manganese. Sediment cores were taken on two occasions, in 1978 and 1997, before and after an incidence of full circulation. The aims of this study are to see how oxic and anoxic conditions in the water column influence stratigraphy and sediment focusing and, to compare cores from 1979 and 1998 to see how measured element fluxes and external events are reflected in the chemical stratigraphy. Element analyses show characteristic stratigraphic patterns that depend on the ability to undergo redox transformations, sorptive properties and chemical equilibria in the anoxic deep waters and porewaters. In sediments from the oxic part of the lake Al, Cr, Co, Ni, Zn Cu, Cd, and Pb were well correlated. Positive correlations are seen between elements associated with primary production and sulphur. In the anoxic part of the lake most metals were positively correlated with carbonate. Phosphorus correlated positively with iron in sediments from oxic waters and negatively with manganese and iron deep-water sediments. Porewater analyses indicate that recycling from the deep-water sediments was negligible. The stratigraphy of lead agrees with the historic variation in atmospheric input and is used as a chronological marker. Assessed deposition rates agree with measurements in sediment traps. Most elements more than double their rates of deposition towards the deepest point of the lake, while sulphur, manganese and carbonate had maxima around the depth of the redoxcline in the water. Variations in the external loading and variable redox conditions in the deep waters explain variations in the chemical composition of recent sediments.