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Unique distribution pattern and δ13C signature of des-A-triterpenoids from Lake Wuliangsu: Source and paleoenvironmental implications.
- Source :
-
Organic Geochemistry . Dec2022, Vol. 174, pN.PAG-N.PAG. 1p. - Publication Year :
- 2022
-
Abstract
- • des- A-triterpenoids from Lake Wuliangsu show a unique distribution pattern and source. • des- A-triterpenoids can track submerged macrophytes in Lake Wuliangsu. • des- A-triterpenoids are impacted by aerobic bacteria activities and photodegradation. des- A-triterpenoids have been widely recognized as indicators of terrestrial vascular angiosperms and microbial activities. However, recent studies also suggested complex sources for des- A-triterpenoids in lakes and peatlands, thus complicating their applications in paleoenvironmental reconstructions. Here we present the occurrences of aliphatic and aromatic des- A-triterpenoids from a ∼160-year sedimentary core in Lake Wuliangsu in the upper reaches of the Yellow River, China. In these sediments, des-A-triterpane was not detected, whereas di-unsaturated des -A-triterpenes are more abundant than mono-unsaturated des -A-triterpenes. The δ13C values of di-unsaturated des -A-triterpenes range from –23.0‰ to –17.6‰, with an average value of –21.0‰. Accordingly, aliphatic des- A-triterpenoids from Lake Wuliangsu show a unique distribution pattern and more positive δ13C signatures compared with those sourced from terrestrial vascular angiosperms. By comparing the concentrations and δ13C values of des- A-triterpenoids with n -alkanes and triterpenoids, we suggest that des- A-triterpenoids from Lake Wuliangsu sediments might be degraded from oleanenone, which was produced by submerged macrophytes. In this sense, aliphatic des -A-triterpenes in Lake Wuliangsu could represent a novel proxy for submerged macrophytes, which would be more precise than those of mid-chain n -alkanes, considering that mid-chain n -alkanes are usually from multiple sources. Our results also demonstrate the importance of strong aerobic bacteria activities and photodegradation for the formation of di-unsaturated des -A-triterpenes. The aromatization process of aliphatic des -A-triterpenes show contrasting variation characteristic with the formation of aliphatic des -A-triterpenes over the past ∼160 years, probably due to different rates (production vs consumption of di-unsaturated des -A-triterpenes) and prerequisites (aerobic vs anaerobic conditions) for these two synthesis pathways. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 01466380
- Volume :
- 174
- Database :
- Academic Search Index
- Journal :
- Organic Geochemistry
- Publication Type :
- Academic Journal
- Accession number :
- 160368227
- Full Text :
- https://doi.org/10.1016/j.orggeochem.2022.104509