Bernd Mycke

Molecular fossils from chemical degradation of macromolecular organic matter

Abstract Hydrogenolysis with rhodium-on-charcoal was found to be an effective method for degrading different types of macromolecular material of geological origin. Between 6 and 70% of coals, kerogens and humic substances were transferred into low-molecular-weight soluble materials. The reaction products contained a series of monomeric and dimeric lignin-derived compounds which strongly suggest intact fossil lignin as their source. The substitutional patterns of the released phenols reflect the type and amount of terrestrial organic matter input and diagenetic alterations. In addition to the lignin constituents, a complete suite of hydrocarbons differing from those of the low-molecular-weight fraction was obtained after hydrogenolysis of the sample material. Hydrocarbons released by the hydrogenolytic degradation technique were attached to the polymeric matrix as monoor polyethers. Deuterium was used in the degradation experiment to evaluate the sites of chemical bonds by which 4-methylsteranes and hopanes are attached to the kerogen matrix. These experiments suggested a linkage of the released molecules with ring A and the side-chain, respectively.

Biomarkers in sedimentary sulfides of precambrian age

Abstract Samples of the Mt Isa formation (Australia, c , 1.5 Ga), and the Shungit formation (U.S.S.R., c . 2.3 Ga) were studied by organic geochemical means. All samples were freed of any low-molecular-weight solvent soluble organic material in order to insure the authenticity of the analysed material. The isolation of biochemical compounds entrapped in sulfides was the major goal of this work. Organic compounds that were entrapped during the early stages of sulfide formation may obviously survive extended periods of time and can be released by a mild hydrogenation of the sulfides. Preliminary investigations of the hydrocarbon fraction indicate n-alkanes, monomethylalkanes, cycloalkanes, and an unknown series of branched alkanes as major constituents. Their distribution patterns show great selectivity with respect to structures and chain lengths of individual compounds. Differences between the hydrogenation reaction product and the sample extract may arise from the release of a different kind of lipid material through dissolution of the sulfides.