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Poster presentation

The laminated sediment record from Laguna Pallcacocha, Ecuador, is widely used as a sensitive recorder of past variability in the El Nino-Southern Oscillation. However, limited knowledge of local meteorology, hydrogeomorphic processes, and the lateral variability of the lacustrine stratigraphy have resulted in some ambiguity in proxy interpretation. In this study, we report new high-resolution meteorological data, hydrogeomorphic mapping of the catchment and geochemistry of the lake’s sediments. We show that the fine clastic layers are deposited from alluvial activity in the catchment related to intensive rainfall events originating from the Pacific. Frequency analyses of the geochemistry of the sediments indicates that the clastic layers in L. Pallcacocha fall into the characteristic ENSO frequency band and most likely record Eastern Pacific and Coastal Pacific El Nino events. We also illustrate that recent debris flow deposition has resulted in an abrupt avulsion of the main fluvial channels, redirecting sediment input between the lake’s two basins and possibly influencing the lithostratigraphy of the sediment package of L. Pallcacocha.

The trace-metal composition of sediments provides important information on (past) environmental conditions, such as bottom water oxygenation, marine productivity, sediment provenance, and pollution. Whereas major and minor elements are often routinely analyzed using X-Ray Fluorescence (XRF) core scanning, analysis of trace metals with the same method is not yet established as a routine procedure. Here, we used a recently developed state-of-the-art XRF detector with a core scanner (Avaatech) to examine the optimal settings for analyzing a suite of trace metals (V, Cr, Ni, Cu, Zn, Mo, and U). Settings were optimized for fast analyses of sediment cores by extensive testing of primary energy settings, filters, and exposure times on two eastern Mediterranean Sea sapropel layers that archive episodes of past sea-floor anoxia. We reveal the following most advantageous (i.e., optimized for analytical accuracy and time efficiency) settings: (1) V, Cr, Ni at 20 kV with aluminum primary beam filter, (2) Cu, Zn, and U at 30 kV with ‘thick’ (125 μm) palladium primary beam filter, and (3) Mo at 50 kV with copper primary beam filter. For these trace elements, generally, ≥30 s of measurement are required for obtaining reliable data. Synthetic mixtures show that matrix effects, which are inherent to XRF analyses, are of particular importance for V. A correction for these matrix effects on V (e.g., using Compton scattering) may be necessary for samples with a large variability in carbonate content. XRF core-scanning measurements on synthetically, laminated sediments show that trace metals with contrasting atomic weights and related XRF penetration depths (V and Mo) can be determined at sub-mm resolution. We show that intensity results from the new XRF detector can be converted into concentrations using multivariate log-ratio calibration, allowing a fast quantitative prediction of sedimentary trace metal content using XRF core scanning.

Sapropels are organic-rich sediment layers deposited in the eastern Mediterranean Sea during precession minima, resulting from an increase in export productivity and/or preservation. Increased freshwater delivery from the African continent resulted in stratification, causing deepwater anoxia, while nutrient input stimulated productivity, presumably at the deep chlorophyll maximum. Previous studies have suggested that during sapropel deposition, nitrogen fixation was widespread in the highly stratified surface waters, and that cyanobacteria symbiotic with diatoms (diatom-diazotroph associations, DDAs) were responsible. Here we analyzed sapropel S5 sediments for heterocyst glycolipids (HGs) from three locations in the eastern Mediterranean. HG biomarkers can differentiate between those heterocystous cyanobacteria that are free living (found predominately in freshwater or brackish environments) and those that are from DDAs (found in marine settings). In our primary core, from a location which would have been influenced by the Nile River outflow, we detected a HG with a pentose (C5) head group specific for DDAs. However, HGs with a hexose (C6) head group, specific to free-living cyanobacteria, were present in substantially (up to 60×) higher concentration. These data suggest that at our study location, free-living cyanobacteria were the dominant diazotrophs, rather than DDAs. The C6 HGs increased substantially at the onset of sapropel S5 deposition, suggesting that substantial seasonal cyanobacterial blooms were associated with a brackish surface layer flowing from the Nile into the eastern Mediterranean. Two additional S5 sapropels were analyzed, one also from the Nile delta region and one from the region between Libya and southwestern Crete. Overall, comparison of the HG distribution in the three S5 sapropels provides evidence that all three locations were initially influenced by surface salinities that were sufficiently low to support free-living heterocystous cyanobacteria. While free-living heterocystous cyanobacteria continued to outnumber DDAs during sapropel deposition at the two Nile-influenced sites, DDAs, indicators of persistent marine salinities, were the dominant diazotrophs in the upper part of the sapropel at the more westerly site. These results indicate that N2 fixation by free-living cyanobacteria offers an important additional mechanism to stimulate productivity in regions with strong river discharge during sapropel deposition.