scholarly journals The Paleoclimate Significance of the δ13C Composition of Individual Hydrocarbon Compounds in the Maoming Oil Shales, China

2021 ◽  
Vol 9 ◽  
Author(s):  
Xinxing Cao ◽  
Zhiguang Song ◽  
Sibo Wang ◽  
Puliang Lyu

Maoming oil shales are typical low-altitude lacustrine sediments that were deposited during the late Paleogene. The hydrocarbon composition and compound-specific stable carbon isotopic composition (δ13C) of organic matter in the profile samples of the oil shales have been analyzed. The results show that algae and aquatic plants are major parent sources of the organic matter in the oil shales associated with a small portion of terrestrial higher plant input. The δ13C composition of the bulk organic matter and the n-alkanes varies greatly on the profile from −26.9 to −15.8‰ and −31.7 to −16.2‰, respectively. While a good positive correlation among the δ13C composition of individual n-alkanes implies that these n-alkanes were originated from the similar source input. The δ13C composition of n-alkanes on the profile displays a positive excursion trend from the bottom to the top, and this excursion was likely related to the general decreasing trend of the partial pressure of atmospheric CO2 (pCO2) during the late Paleogene. The δ13C composition of the C30-4-methyl steranes ranges from −11.9 to −6.3‰, which is suggestive of Dinoflagellates-related source input. Coincidently, the high abundance C33-botryococcanes were detected in the samples on the top section of the profile and display an extremely positive carbon isotopic composition of −4.5 to −8.4‰, suggesting that the lower partial pressure of atmospheric CO2 had triggered a bicarbonate consumption mechanism for Botryococcus braunii B. Therefore, the δ13C composition of n-alkanes and C33-botryococcanes and their profile variation suggest that a general declining process associated with fluctuation in the partial pressure of atmospheric CO2 is likely the major reason for the rapid climatic changes toward the end of the late Paleogene.

1992 ◽  
Vol 6 ◽  
pp. 163-163
Author(s):  
Fabien Kenig ◽  
Brian Popp ◽  
Roger Summons

To understand the processes controlling production, accumulation, and preservation of organic matter in the Lower Oxford Clay (LOC), we determined the hydrogen index (HI), the oxygen index (OI), the Tmax (from Rock-Eval), the content of total organic carbon (TOC), total carbon and total sulfur, and the carbon isotopic composition of bulk organic matter from 160 samples collected from 6 different quarries and one continuous core. With concentrations of TOC varying between 0.5% and 16.6%, the LOC is an organic-rich shale. For samples dominated by organic matter of phytoplanktonic origin, the hydrogen and oxygen indices and the Tmax (~418°) indicate low levels of maturity, and, thus, the shallow burial of the LOC through geologic time.Two main sources of organic matter can be distinguished: a major phytoplanktonic source with high HI and low OI and a minor terrestrial source with low HI and high OI. A third group, represented by samples with low HI and low OI, consists mainly of altered materials from the Middle Oxford Clay and the LOC. Selection of samples for chemical analysis was based on the macrofaunal assemblages defined by Duff (1975). These various biofacies are characterized by specific organic geochemical features indicating the relationship between conditions affecting faunal assemblages and those controlling accumulation and preservation of organic matter. For example, Duff's ‘deposit feeder shales', which are dominated by epifaunal bivalves and are depleted in infaunal organisms, exhibit the highest concentration and best preservation of marine organic matter, with an average TOC of 6.8% for 56 samples analyzed. The preservation of such organic matter requires a dysaerobic water column and a high sedimentation rate.Carbon isotopic compositions within the ‘deposit feeder shale’ biofacies (−27.6 to −23.2±) appear to have been controlled by the intensity of primary productivity. The highest-TOC, marine-dominated, 13C-rich samples reflect photosynthetic drawdown of dissolved-CO2 level, and, thus, originated in highly productive environments. On the other hand, variations in the carbon isotopic composition of organic matter in shell beds (−27.5 to −26±) probably reflect heterotrophic reworking of the organic matter, winnowing of the sediments, and mixing with a source of organic matter enriched in 13C, such as wood (δ13C from −25 to −23±). Such mixing phenomena may also explain the high variability of the carbon isotopic compositions of TOC-depleted and altered samples from the Middle and Upper Oxford Clay.The environment of deposition of the LOC would be characterized by the alternation of two major conditions: 1) periods of high productivity, dysoxic water column and high sedimentation rate leading to the development of organic-rich shales dominated by phytoplanktonic organic matter, and 2) periods of low productivity, oxic water column and high current activity implying winnowing and alteration of organic matter, and leading to the formation of shell beds where marine and terrestrial organic matter are mixed.


2010 ◽  
Vol 7 (9) ◽  
pp. 2959-2973 ◽  
Author(s):  
J. W. H. Weijers ◽  
G. L. B. Wiesenberg ◽  
R. Bol ◽  
E. C. Hopmans ◽  
R. D. Pancost

Abstract. Branched Glycerol Dialkyl Glycerol Tetraethers (GDGTs) are membrane spanning lipids synthesised by as yet unknown bacteria that thrive in soils and peat. In order to obtain more information on their ecological niche, the stable carbon isotopic composition of branched GDGT-derived alkanes, obtained upon ether bond cleavage, has been determined in a peat and various soils, i.e. forest, grassland and cropland, covered by various vegetation types, i.e., C3- vs. C4-plant type. These δ13C values are compared with those of bulk organic matter and higher plant derived n-alkanes from the same soils. With average δ13C values of −28‰, branched GDGTs in C3 soils are only slightly depleted (ca. 1‰) relative to bulk organic carbon and on average 8.5‰ enriched relative to plant wax-derived long-chain n-alkanes ( nC29–nC33). In an Australian soil dominantly covered with C4 type vegetation, the branched GDGTs have a δ13C value of −18‰, clearly higher than observed in soils with C3 type vegetation. As with C3 vegetated soils, branched GDGT δ13C values are slightly depleted (1‰) relative to bulk organic carbon and enriched (ca. 5‰) relative to n-alkanes in this soil. The δ13C values of branched GDGT lipids being similar to bulk organic carbon and their co-variation with those of bulk organic carbon and plant waxes, suggest a heterotrophic life style and assimilation of relatively heavy and likely labile substrates for the as yet unknown soil bacteria that synthesise the branched GDGT lipids. However, a chemoautotrophic lifestyle, i.e. consuming respired CO2, could not be fully excluded based on these data alone. Based on a natural labelling experiment of a C3/C4 crop change introduced on one of the soils 23 years before sampling and based on a free-air CO2 enrichment experiment with labelled CO2 on another soil, a turnover time of ca. 18 years has been estimated for branched GDGTs in these arable soils.


2010 ◽  
Vol 7 (3) ◽  
pp. 3691-3734 ◽  
Author(s):  
J. W. H. Weijers ◽  
G. L. B. Wiesenberg ◽  
R. Bol ◽  
E. C. Hopmans ◽  
R. D. Pancost

Abstract. Branched Glycerol Dialkyl Glycerol Tetraethers (GDGTs) are membrane spanning lipids synthesised by as yet unknown bacteria that thrive in soils and peat. In order to obtain more information on their ecological niche, the stable carbon isotopic composition of branched GDGT-derived alkanes, obtained upon ether bond cleavage, has been determined in various soils, i.e. peat, forest, grassland and cropland, covered by various vegetation types, i.e., C3- vs. C4-plant type. These δ13C values are compared with those of bulk organic matter and higher plant derived n-alkanes from the same soils. With average δ13C values of −28‰, branched GDGTs in C3 soils are only slightly depleted (ca. 1‰) relative to bulk organic carbon and on average 8.5‰ enriched relative to plant wax-derived long-chain n-alkanes (nC29–nC33). In an Australian soil covered with C4 type vegetation, the branched GDGTs have a δ13C value of −18‰, clearly higher than observed in soils with C3 type vegetation. As with C3 vegetated soils, branched GDGT δ13C values are slightly depleted (1‰) relative to bulk organic carbon and enriched (ca. 5‰) relative to n-alkanes in this soil. The δ13C values of branched GDGT lipids being similar to bulk organic carbon and their co-variation with those of bulk organic carbon and plant waxes, suggest a heterotrophic life style and assimilation of relatively heavy and likely labile substrates for the as yet unknown soil bacteria that synthesise the branched GDGT lipids. However, a chemoautotrophic lifestyle, i.e. consuming respired CO2, could not be fully excluded based on these data alone. Based on a natural labelling experiment of a C3/C4 crop change introduced on one of the soils 23 years before sampling and based on a free air CO2 enrichment experiment with labelled CO2 on another soil, a turnover time of ca. 17 years has been estimated for branched GDGTs in these arable soils.


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