Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Diagenesis at the molecular level

Epimerization (see Section 2.1.3) converts the single, biologically conferred configuration at a stereogenic centre into an equilibrium mixture of the two possible [Pg.175]

It was noted in Section 3.3.1 that phytoplankton and their remains upon death sink only very slowly, allowing ample opportunity for predation by zooplankton [Pg.175]

Isomerization at a stereogenic centre in a biomarker is an example of a reversible reaction in which reactant and product have similar energies. [Pg.176]

Fatty acid distributions can be affected by microbial oxidation in sediments, so care must be exercised when certain components are used as source indicators. For example, (3-hydroxy fatty acids are produced from (3-oxidation of saturated fatty acids. In addition, C0-oxidation of saturated fatty acids to CO-hydroxy acids and of CO-hydroxy acids to a,CO-diacids is performed by yeasts (unicellular fungi, mainly belonging to the as-comycetes) and bacteria. Consequently, while the long-chain ( C22) CO-hydroxy acids are reliable indicators of higher plant sources, the short-chain components [Pg.179]

The main inputs of chlorophyll-derived compounds to sediments under oxidizing conditions are usually pyrophaeophorbides, due to the activity of zooplank- [Pg.180]


See other pages where Diagenesis at the molecular level is mentioned: [Pg.174]   


SEARCH



Diagenesis

Molecular level

© 2024 chempedia.info