A set of oxidized and unoxidized sediment intervals from the f-turbidite identified in two piston cores from the Madeira Abyssal Plain (MAP) was analyzed for calcium carbonate, total organic carbon (TOC), total nitrogen (TN), stable carbon composition of TOC (δ 1 3 C T O C ), total hydrolyzable amino acids (THAA), total neutral sugars (TSUG), lignin phenols (LIG), two different lipid biomarkers of marine phytoplankton origin and vascular plantwax n-alkanes and n-acids. Comparison shows changes for all properties depicting the effect of post-depositional, aerobic oxidation. The oxidation process re-mineralized approximately 80% of the TOC and approximately 60% of the TN in the original deposit and left the residual organic matter depleted in 1 3 C by 1.7-2.9‰. THAA and TSUG account for 10% or less of the TOC in all samples leaving approximately 90% of the TOC chemically unidentified. THAA, TSUG, LIG, marine phytoplankton biomarkers and plantwax n-acids were lost from the oxidized deposit to an extent as great as that for TOC. Two non-protein amino acids (β-alanine and γ-aminobutyric acid) and plant wax n-alkanes displayed much less degradation (9-37%) and concentrated 3.3-4.8 times relative to TOC by the oxidation process. These observations show that both marine and terrestrial components contribute to the re-mineralized TOC fraction. A binary mixing approach was used to model quantitatively the change in δ 1 3 C T O C and plantwax n-alkane concentration. Results suggest that terrestrial organic carbon contributes approximately 15% to the TOC content of the original turbidite, its abundance increases approximately 2-4 times as a consequence of the oxidation process and approximately 40 and 90% of the terrestrial and marine component of TOC in the original turbidite, respectively, was destroyed by the oxidation process. Although selective preservation of terrestrial relative to marine organic carbon is a well-documented phenomenon in sedimentary processes, this study represents the first attempt to assess the sensitivity of terrestrial organic matter to oxidative degradation in a sedimentary environment.