Isotopic analysis (δ13C and δ2H) of lignin methoxy groups in forest soils to identify and quantify lignin sources

• Verfasst von: Cox, Terry [VerfasserIn]
• Verfasst von: Wieland, Anna [VerfasserIn]
• Verfasst von: Greule, Markus [VerfasserIn]
• Verfasst von: Keppler, Frank [VerfasserIn]
• Verfasst von: Einbock, Annika [VerfasserIn]
• Verfasst von: Alewell, Christine [VerfasserIn]
• Titel: Isotopic analysis (δ13C and δ2H) of lignin methoxy groups in forest soils to identify and quantify lignin sources
• Verf.angabe: Terry Cox, Anna Wieland, Markus Greule, Frank Keppler, Annika Einbock, Christine Alewell
• E-Jahr: 2024
• Jahr: 1 November 2024
• Umfang: 10 S.
• Illustrationen: Illustrationen
• Fussnoten: Im Titel sind die Zahlen 13 und 2 hochgestellt ; Online verfügbar: 24. Juli 2024, Artikelversion: 29. Juli 2024 ; Gesehen am 27.03.2025
• Titel Quelle: Enthalten in: The science of the total environment
• Ort Quelle: Amsterdam [u.a.] : Elsevier Science, 1972
• Jahr Quelle: 2024
• Band/Heft Quelle: 949(2024) vom: Nov., Artikel-ID 175025, Seite 1-10
• ISSN Quelle: 1879-1026
• DOI: doi:10.1016/j.scitotenv.2024.175025
• Datenträger: Online-Ressource
• Sprache: eng
• Sach-SW: Carbon soil dynamics
• Sach-SW: MixSIAR
• Sach-SW: Serine
• Sach-SW: Source apportionment
• Sach-SW: Stable isotopes
• K10plus-PPN: 1920708936

Abstract

The relative apportion of above and below ground carbon sources is known to be an important factor in soil organic matter formation. Although lignin is the most abundant aromatic plant material in the terrestrial biosphere, our understanding of lignin source contributions to soil organic matter (SOM) is limited due to the complex molecular structure and analysis of lignin. In this study, we novelly apply the dual isotopic analysis (δ13C and δ2H values) of lignin methoxy groups (LMeO) with the Bayesian mixing model, MixSIAR, to apportion lignin sources in two contrasting soil types, a podzol and a stagnosol. Results of the isotopic analysis of LMeO demonstrate the ability of δ2H LMeO values to discriminate between above and below ground lignin sources, while δ13C LMeO values discriminated between photosynthesising and non-photosynthesising tissues. In the stagnosol subsurface horizons, a decreasing proportion of the leaf litter lignin was observed with increasing organic matter degradation, cumulating in the Ah horizon being dominated by lignin from roots. The podzol sites indicated a similar reduction in leaf litter lignin with an increase in organic matter degradation and depth. However, the Ah horizon was shown to accumulate lignin from the above ground woody material. Furthermore, given the significant abundance of LMeO groups in the terrestrial biosphere and the extremely depleted δ13C LMeO values in leaf litter, we employed a mass balance approach to determine the extent in which the 13C bulk enrichment generally associated with isotopic fractionation during organic matter decomposition can be attributed to the shift in lignin sources. Analysis reveals that 14 % and 11 % of bulk 13C enrichment can be attributed to the transition in LMeO sources from leaf litter to roots in the stagnosol and podzol, respectively. Thus, models relying on 13C enrichment with depth as an indicator of carbon turnover may be partially overestimating rates.