Spatial variations in phosphorus (P) fractionation, sediment geochemistry, and sorptive properties for P are assessed to test the hypothesis that these sediment properties vary within the lake and are governed by different land uses in the watershed. The dynamic equilibrium between P in sediment and water is investigated using sorption-desorption isotherms. Sediments in the littoral zone were rich in iron (Fe), aluminium (Al), and clay material in comparison to sediments from the lake proper and thus had better abilities to sorb and retain P. In the limnetic zone, there was an increasing abundance of primary minerals, and the fraction of apatite-P was high, while the level of total P was low. The amount of labile adsorbed P (LAP) in the littoral sediments varied because of contrasting land use in the sub-catchments draining into different parts of the lake. Sediments in areas where forest streams enter the lake contained significantly more LAP than sediments in areas impacted by agricultural influenced streams. Internal P loading from sediments predominantly originating from forest streams is mainly governed by sediment resuspension. The dominant P pool in sediments near the inlets of agriculturally influenced streams was non-apatite inorganic P, of which the Fe-bound is a potentially important source of P under anoxic conditions.
Deterioration of oxygen conditions in water below the halocline has been observed in the Baltic Sea. Deoxygenation is linked to the reduced frequency and volume of inflows of highly saline surface water from the North Sea (major Baltic inflows-MBIs) in the second half of the twentieth century and the increased organic matter respiration due to eutrophication. In the present study, the impact of worsening oxygen conditions on pyrite content in the Gdańsk Deep (max. depth of 118 m, southern Baltic Sea) sediments was determined. Geochemical parameters (acid volatile sulfides, pyrite sulfur, reactive iron, organic carbon, sedimentation rate and sediment age) were analyzed in relation to the variation in bottom water oxygen concentration and the occurrence of MBI. The obtained results demonstrate that pyrite content in the study area decreased after 1960. The declining pyrite content coincided with the deterioration of oxygen conditions (concentration \ 2 ml l-1) in bottom water. In the same period, reactive iron concentration decreased and organic carbon increased in sediment. In the period 1616-1960, average pyrite accumulation rate was 322 lmol m-2 day-1. In the subsequent years, its average accumulation rate decreased to 210 lmol m-2 day-1. Fluctuations of oxygenation of bottom water in the study area were manifested by highly variable degree of pyritization (36 ± 11%) and particulate organic carbon to pyrite sulfur ratio (2.8-37).
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