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Elsevier, Palaeogeography, Palaeoclimatology, Palaeoecology, (385), p. 137-151, 2013

DOI: 10.1016/j.palaeo.2012.12.007

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A biomarker study of depositional paleoenvironments and source inputs for the massive formation of Upper Cretaceous lacustrine source rocks in the Songliao Basin, China

Journal article published in 2013 by Zhiguang Song, Yin Qin, Simon C. George ORCID, Li Wang, Jiangtao Guo, Zihui Feng
This paper is available in a repository.
This paper is available in a repository.

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Abstract

The abundance and composition of total organic carbon, aliphatic and aromatic hydrocarbons including biomarkers, and the δ 13 C composition of total organic matter and individual compounds in core samples of the Nenjiang Formation from the SK-1 borehole of the Songliao Basin provide information on the paleoenvironmental conditions of lacustrine sediments formed during the Upper Cretaceous. The distribution of n-alkanes, and their δ 13 C composition, and 4-methylsteranes and dinosteranes in the first member of the Nenjiang Formation (K 2 n 1) indicate that the organic matter largely originated from algal organisms and is dominated by types I and II kerogen. The occurrence of gammacerane, aryl isoprenoids isorenieratane and low pristane/phytane and diasterane/sterane ratios further suggest a salinity stratified water column associated with anoxic bottom waters, as well as possible photic zone oxygen depletion conditions during major source rock deposition of the K 2 n 1. The organic geochemical data also indicate significantly different depositional environments for the second member of the Nenjiang Formation (K 2 n 2) sediments, which are interpreted to have been deposited under a uniform salinity (non-stratified) oxic water column. Consequently, although the organic matter in the K 2 n 2 sediments was largely derived from algal and bacterial sources, the kerogen types are dominantly IIb and III due to the oxidative degradation of organic matter, combined with a gradual increase in land–plant input. Furthermore, the occurrence and shift of two saw-toothed distribution patterns of the δ 13 C composition of C 29 to C 33 n-alkanes, with " W " and " M " patterns being isotopically heavy odd-and even-numbered alkanes, respectively, is suggestive of organic input shift or an unknown mechanism of carbon uptake or isotopic fractionation. In particular, the heavy even carbon numbered high molecular weight n-alkanes is rare and needs further investigation.