Biomarkers in turbidites at ODP Sites 157-951 and 157-952


Autoria(s): Hoefs, Marcel JL; Rijpstra, W Irene C; Sinninghe Damsté, Jaap S
Cobertura

MEDIAN LATITUDE: 31.354755 * MEDIAN LONGITUDE: -24.673636 * SOUTH-BOUND LATITUDE: 30.790800 * WEST-BOUND LONGITUDE: -24.870600 * NORTH-BOUND LATITUDE: 32.031500 * EAST-BOUND LONGITUDE: -24.509500 * DATE/TIME START: 1994-08-13T11:40:00 * DATE/TIME END: 1994-08-20T11:00:00

Data(s)

15/12/2002

Resumo

Free and ester-bound lipid biomarkers were analysed in oxidised and unoxidised parts of four distinct turbidites from the Madeira Abyssal Plain (MAP), which contained 1 to 2% organic carbon homogeneously distributed throughout the turbidites at the time they were deposited. These turbidites are well suited to study the effects of oxic degradation on lipid biomarkers without the complicating influence of varying organic matter sources, sedimentation rates, or bioturbation. One sample from the oxidised turbidite was compared with two samples from the unoxidised part of each turbidite. Postdepositional oxic degradation decreased concentrations of biomarkers by several orders of magnitude. The ester-bound lipids were degraded to a far lesser extent than their free counterparts were. The extent of degradation of different compounds differed substantially. Within a specific class of biomarkers, degradation also took place to a different extent, altering their distributions. This study shows that oxic degradation of the organic matter may have a profound effect on the biomarker fingerprint and may result in a severe bias in, for example, the interpretation of organic matter sources and the estimation of the palaeoproductivity of specific groups of phytoplankton.

Formato

application/zip, 11 datasets

Identificador

https://doi.pangaea.de/10.1594/PANGAEA.708704

doi:10.1594/PANGAEA.708704

Idioma(s)

en

Publicador

PANGAEA

Direitos

CC-BY: Creative Commons Attribution 3.0 Unported

Access constraints: unrestricted

Fonte

Supplement to: Hoefs, Marcel JL; Rijpstra, W Irene C; Sinninghe Damsté, Jaap S (2002): The influence of oxic degradation on the sedimentary biomarker record I: Evidence from Madeira abyssal plain turbidites. Geochimica et Cosmochimica Acta, 66(15), 2719-2735, doi:10.1016/S0016-7037(02)00864-5

Palavras-Chave #157-951B; 157-952; 157-952A; Age model; Alkenone, C37:2; Alkenone, C37:3; Alkenone, C38:3; C16 n-A.ol/sed; C18 n-A.ol/sed; C20 n-A.ol/sed; C22 n-A.ol/sed; C24 n-A.ol/sed; C26 n-A.ol/sed; C28 n-A.ol/sed; C30 n-A.ol/sed; C37:2; C37:3; C38:3; Canarias Sea; Carb; Carbon, organic, total; Carbonates; Chromatographic; Comment; COMPCORE; Composite Core; Depth; Depth, bottom/max; DEPTH, sediment/rock; Depth, top/min; Depth bot; Depth top; DRILL; Drilling/drill rig; for c37:2 alkenone (ii); for c37:3 alkenone (i); for c38:2 alkenone (iii); for n-alkanol c16; for n-alkanol c20; for n-alkanol c22; for n-alkanol c24; for n-alkanol c26; for n-alkanol c28; for n-alkanol c30; for n-alkanol cl8; for n-fatty acid c14; for n-fatty acid c15; for n-fatty acid c16; for n-fatty acid c17; for n-fatty acid c18; for n-fatty acid c20; for n-fatty acid c22; for n-fatty acid c24; for n-fatty acid c26; for n-fatty acid c28; for n-fatty acid c30; Joides Resolution; Label; Leg157; Lipid extraction (Wolff et al., 1995); n-Alkanol C16 per unit sediment mass; n-Alkanol C18 per unit sediment mass; n-Alkanol C20 per unit sediment mass; n-Alkanol C22 per unit sediment mass; n-Alkanol C24 per unit sediment mass; n-Alkanol C26 per unit sediment mass; n-Alkanol C28 per unit sediment mass; n-Alkanol C30 per unit sediment mass; n-C14 FA; n-C15 FA; n-C16 FA; n-C17 FA; n-C18 FA; n-C20 FA; n-C22 FA; n-C24 FA; n-C26 FA; n-C28 FA; n-C30 FA; n-fatty acid C14; n-fatty acid C15; n-fatty acid C16; n-fatty acid C17; n-fatty acid C18; n-fatty acid C20; n-fatty acid C22; n-fatty acid C24; n-fatty acid C26; n-fatty acid C28; n-fatty acid C30; North Atlantic Ocean; Ocean Drilling Program; ODP; ODP sample designation; of 17b,21b(h)-bishomohopan-32-ol(XIX), %; of 17b,21b(h)-bishomohopanoic acid (XVIII), %; of 17b,21b(h)-homohopan-31-ol (XVII), %; of 23,24-dimethyl-5a-cholest-22-en-3b3-ol, %; of 23,24-dimethyl-5a-cholestanol, %; of 24-ethyl-5a-cholest-22-en-3b-ol, %; of 24-ethyl-5 a-cholestanol, %; of 24-ethyl-cholest-5-en-3b-ol (XII), %; of 24-methyl-5a-cholest-22-en-3b-ol (XIII), %; of 24-methyl-5a-cholestanol (IX), %; of 24-methyl-cholest-5,22-dien-3b-ol (XIV), %; of 24-methyl-cholest-5-en-3b-ol, %; of 4,23,24-trimethyl-5a-cholest-22-en-3b-ol (XII), %; of 4,23,24-trimethyl-5a-cholestan-3b-ol (XI), %; of 4,24-dimethyl-5a-cholest-22-en-3b-ol, %; of 4-methyl-24-ethyl-5a-cholestan-3b-ol (X), %; of 5a-cholest-22-en-3/3-ol, %; of 5a-cholest-5-en-3b-ol, %; of 5a-cholesta-5,22-dien-3b-ol, %; of 5a-cholestanol, %; of bound lipids, for dry wieght; of diols and keto-ols, %; of dotriacontane-1,15-diol (VI), %; of free lipids, for dry wieght; of hentriacontane, %; of heptacosane, %; of hexahydrofarnesylaceton, %; of iso-loliolide, %; of loliolide (XX), %; of n-alkanes, %; of nonacosane, %; of octacosane-1,15-diol (IV), %; of phytol, %; of steroids, %; of taraxer-14-en-3b-ol (XV), %; of tetrahymanol (XVI), %; of triacontan-15-one-1-ol (VII), %; of triacontane-l,15-diol (V), %; of tricyclic biphytane diol (VIII), %; of trisnorhopan-21-one, %; of triterpenoids, %; of tritriacontane, %; Pf; Preserv; Preservation; Preservation factor; redox state; Samp com; Sample code/label; Sample comment; TOC; Yield
Tipo

Dataset