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a
Fossil dicot leaf
I
Pr1
m/z
130+131
G2
G3
G1
G5
?
P1
I
B3
G4
B2
N
Pr2
Ps2
P2
2
0
B4
Ps1
23
25
28
G5
m/z
154+168+180+182+194+196
S1
S2
Pr1
S3
b
Fossil conifer
B2
Pr1
?
Ps?
Ps2
P1
B4
I
P2
G5
G4
G1
B3
G2
Pr2
G3
Ps1
N
17
23
29
20
33
Retention time
Fig. 4.4
(
a
) Partial py-GC-MS total ion current chromatogram of fossil dicotyledon leaf indicat-
ing the presence of moieties related to benzene derivatives, polysaccharides, phenols, lignin and
protein together with n-alkane/n- alk-1-ene homologues, number indicating the carbon chain
length. m/z 130 + 131 reveals the presence of methyl indole. m/z 154 + 168 + 180 + 182 + 194 + 196
reveals the distribution of syringyl moieties. (
b
) Partial py-GC-MS total ion current chromatogram
of fossil conifer, showing released moieties related to benzene derivatives, polysaccharides, phe-
nols, lignin and protein, together with n-alkane/n-alk-1-ene homologues.
B2
: dimethylbenzene,
B3
: trimethylbenzene,
B4
: tetramethylbenzene,
N
: naphthalene. Guaiacyl related units.
G1
:
2-methoxyphenol,
G2
: 4-methyl-2-methoxyphenol,
G3
: 4-ethyl-2-methoxyphenol,
G4
: 4-ethenyl-
2-methoxyphenol,
G5
: 3-allyl-6-methoxyphenol. Syringyl related units.
S1
: 4-ethyl-2,6-
dimethoxyphenol,
S2
: 2,6-dimethoxy-4-vinylphenol,
S3
: 4-ally-2,6-dimethoxyphenol.
Pr1
:
Prist-1-ene.
P1
: methylphenol,
P2
: dimethylphenol. Polysaccharide pyrolysis products:
Ps1
:
2-methyl-2-cyclopenten-2-one,
Ps2
: 2,3-dimethyl cyclopenten-1-one,
Ps??
: unknown moiety
TMAH assisted pyrolysis was conducted on the fossil conifer to characterise
further the fossil composition and determine the lipid distribution. The thermochemol-
ysis trace (Fig.
4.5
) reveals methylated equivalents of the lignin moieties, aromatics
(see Hatcher and Clifford
1994
; Hatcher et al.
1995
; Clifford et al.
1995
; Almendros
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