ABSTRACT
In closed-basin lakes, sediment porewater salinity can potentially be used as a conservative tracer to reconstruct past fluctuations in lake level. However, until now, porewater salinity profiles did not allow quantitative estimates of past lake-level changes because, in contrast to the oceans, significant salinity changes (e.g., local concentration minima and maxima) had never been observed in lacustrine sediments. Here we show that the salinity measured in the sediment pore water of Lake Van (Turkey) allows straightforward reconstruction of two major transgressions and a major regression that occurred during the last 250 ka. We observed strong changes in the vertical salinity profiles of the pore water of the uppermost 100 m of the sediments in Lake Van. As the salinity balance of Lake Van is almost at steady-state, these salinity changes indicate major lake-level changes in the past. In line with previous studies on lake terraces and with seismic and sedimentological surveys, we identify two major transgressions of up to +105 m with respect to the current lake level at about 135 ka BP and 248 ka BP starting at the onset of the two previous interglacials (MIS5e and MIS7), and a major regression of about -200 m at about 30 ka BP during the last ice age.
ABSTRACT
During the éLEMO endeavour (a research project in which the Russian MIR submersibles were used for studying Lake Geneva) four sediment cores were retrieved on a transect from the delta of the Rhone River towards the profundal part of the lake. The degradation pathways of organic material (OM) were investigated considering different electron acceptors. Essentially, OM at the delta sites had a higher fraction of terrestrial material than the lake sites indicated by higher C/N ratios, and higher long-chain n-alkane and alcohol concentrations. The concentrations of chlorins were higher at the distant sites indicating more easily degradable OM in the sediments. However, the chlorin index that was used to determine the degradation state of the OM material indicated that pigment derived OM of deltaic sediments was less degraded than that of the profundal sediments. The fluxes of reduced species from the sediments decreased from the delta to the profundal for CH4 (from 2.3 to 0.5 mmol m(-2) d(-1)) and NH4(+) (from 0.31 to 0.13 mmol m(-2) d(-1)). Fluxes of Fe(ii) and Mn(ii), however, increased although they were generally very low (between 9 × 10(-5) and 7.6 × 10(-3) mmol m(-2) d(-1)). Oxygen concentration profiles in the pore waters revealed lower fluxes close to the river inflow with 4.3 and 4.1 mmol m(-2) d(-1) compared to two times higher fluxes at the profundal sites (8.8 and 8.2 mmol m(-2) d(-1)). The rates for totally mineralized OM (Rtotal) at the shallower sites (4.7 mmol C m(-2) d(-1)) were only half of those of the deeper sites (9.7 mmol C m(-2) d(-1)). Accordingly, not only the rates but also the mineralization pathways differed between the shallow and profundal sites. Whereas only 0-6% of the OM was mineralized aerobically at the shallow sites (since almost all O2 was used to oxidize the large flux of CH4 from below) the situation was reversed at the deeper sites and the fraction of aerobically degraded OM was 72-78%. We found a better efficiency in CH4 production per carbon equivalent deposited at the deeper sites as a result of the higher degradability of the mainly autochthonous OM in spite of the lower deposition rate and the higher degradation state of the OM compared to the delta sites.
