Fig. 3: Reconstructed total ion chromatogram of the pyrogram (pyrolysis profile) (610 °C for 10 s) of sample DL5838, after thermal desorption (310 °C for 10 s). | Nature Communications

Fig. 3: Reconstructed total ion chromatogram of the pyrogram (pyrolysis profile) (610 °C for 10 s) of sample DL5838, after thermal desorption (310 °C for 10 s).

From: Human consumption of seaweed and freshwater aquatic plants in ancient Europe

Fig. 3

Key: Peak identities (x indicates carbon chain length): filled squares, Cx indicates alkenes; filled circles, Cx indicates alkanes; open diamonds, Cx:y indicates acyclic nitriles; blue filled hexagons indicates alkyl pyridines; green filled pentagons indicates alkyl pyrroles (with alkyl chain length above, Cx); filled hexagons with filled circles attached indicates alkyl phenols; open pentagons with numerals inside indicates carbohydrate pyrolysis markers, 1 is 2-methylfuran, 2 is 2-methyl-2-cyclopenten−1-one and 3 is 2,3-dimethyl-2-cyclopentene−1-one. Also shown are the structures of twelve aromatic compounds identified: pyridine, pyrrole, toluene, styrene, benzonitrile, phenol, indene, benzyl nitrile, benzenepropanenitrile, indole, 3-methylindole (skatole) and 3-ethylindole. CO2 indicates carbon dioxide. Inset displays a reconstructed total ion chromatogram of the thermal desorption profile (310 °C for 10 s) of this sample. Peak identities: BPN indicates a benzenepropanenitrile derivative; open diamond, Cx:y indicates an acyclic nitrile. Also shown are four aromatic compounds: pyridine, pyrrole, benezenepropanenitrile and indole. CO2 indicates carbon dioxide.

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