2006
DOI: 10.1016/j.jaap.2005.03.009
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δ13C values of pyrolysis products from cellulose and lignin represent the isotope content of their precursors

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Cited by 44 publications
(37 citation statements)
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“…After coupling pyrolysis to compound-specific isotope ratio mass spectrometry (GC-IRMS), the isotopic content of individual pyrolysis products were measured (Gleixner and Schmidt 1998;Schulten and Gleixner 1999). Most interestingly, the 13 C isotope ratios of the volatile pyrolysis products mirror the isotopic content of their non-volatile precursors (Steinbeiss et al 2006). In consequence, this technique can be used to determine the turnover and recycling of molecular fragments of soil organic matter using isotopic labeling.…”
Section: Origin and Turnover Of Organic Matter Found In Soilmentioning
confidence: 99%
“…After coupling pyrolysis to compound-specific isotope ratio mass spectrometry (GC-IRMS), the isotopic content of individual pyrolysis products were measured (Gleixner and Schmidt 1998;Schulten and Gleixner 1999). Most interestingly, the 13 C isotope ratios of the volatile pyrolysis products mirror the isotopic content of their non-volatile precursors (Steinbeiss et al 2006). In consequence, this technique can be used to determine the turnover and recycling of molecular fragments of soil organic matter using isotopic labeling.…”
Section: Origin and Turnover Of Organic Matter Found In Soilmentioning
confidence: 99%
“…Pyrolysis was carried out under helium for 9.9 s at 500 • C with a Curie point Pyrolyzer 0316 (Thermo Fisher, USA). Volatile pyrolysis products were separated by gas chromatography (HP 5890, Germany) with a BPX5 capillary column (length, 60 m; inner diameter, 0.32 mm; film thickness, 1 µm; SGE, Germany) and analyzed using an ion trap mass spectrometer (Thermo Fisher, GCQ, USA) (Steinbeiss et al, 2006).…”
Section: Analytical Techniquesmentioning
confidence: 99%
“…As the δ 13 C of the respective products following charring of isolated cellulose and lignin (e.g. levoglucosan), is equivalent to that of their precursors (Steinbeiss et al, 2006), the reduction in δ 13 C during production of pine charcoal may result from a greater contribution of isotopically lighter lignin-derived carbon to the developing charcoal structure. The reduction in δ 13 C over 400ºC is unlikely to result from continued -19 -removal of cellulose, as near complete thermal degradation of aliphatic-C has occurred.…”
Section: δ 13 C Variations During Charcoal Formationmentioning
confidence: 99%