dc.creatorD'Angelo, José A.
dc.creatorWerner-Zwanziger, U.
dc.creatorHelleur, R.
dc.creatorZodrow, E. L.
dc.date2010
dc.date2010
dc.date2011-04-08T03:00:00Z
dc.identifierhttp://sedici.unlp.edu.ar/handle/10915/16853
dc.identifierisbn:978-987-95849-7-2
dc.descriptionDespite the abundance of detached seed-fern ovules (Euramerican and Cathaysian floral provinces, Pennsylvanian - Permian) as compression / impression, their palaeobiochemistry remains unknown. The Late Pennsylvanian strata of the Sydney Coalfield, Canada, have yielded numerous ovulate trigonocarpalean compressions, 6-8cm long, with preserved cuticles assigned to Trigonocarpus grandis (Lesquereux) Cleal et Zodrow. The macerated cuticles are analyzed by Fourier Transform Infrared spectroscopy (FTIR), Carbon-13 Nuclear Magnetic Resonance (<sup>13</sup>C NMR), and Pyrolysis Gas Chromatography-mass spectrometry (Py-GC-MS). FTIR and <sup>13</sup>C NMR data reveal a predominantly aliphatic structure including C-H groups (with or without hetero-substitution such as in alkyl and aryl alcohols, ethers, esters, and ketones). Larger CH<sub>2</sub>/CH<sub>3</sub> ratios (above 20) suggest the presence of long and straight aliphatic side chains linked to the main macromolecular structure. Other groups present include C-O (in phenols and phenoxy structures, and aryl and alkyl ethers and alcohols), C=O carbonyl groups (in carboxylic acids and conjugated and highly conjugated structures such as ketones), C=C (in aromatic carbon structures with and without bridging to other carbon groups), and O-H (in aliphatic or aromatic alcohols). In addition, <sup>13</sup>C NMR shows, compared to other cuticles in related seed ferns, a high amount of acetal groups as they occur in di- and polysaccharides. In agreement with FTIR and NMR results, Py-GC-MS data show the presence of highly aliphatic molecules (alkanes/alkenes) with carbons between C<sub>4</sub> and C<sub>8</sub> (including a complex mixture of mono and di unsaturated hydrocarbon isomers up to C<sub>8</sub>). Other compounds detected include benzene and toluene. However, the most striking chemical feature of the pyrolysates markers is the presence of 5 isomers of C<sub>5</sub>H<sub>8</sub> including isoprene (0.5 - 1.0 % abundance). The latter could be derived from some tocopherol precursor (vitamin E-like compound). If confirmed, this is the earliest chemical evidence for the presence of isoprenoids in vascular plants.
dc.descriptionSesiones libres
dc.descriptionFacultad de Ciencias Naturales y Museo
dc.formatapplication/pdf
dc.languageen
dc.rightshttp://creativecommons.org/licenses/by-nc-sa/4.0/
dc.rightsCreative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)
dc.subjectCiencias Naturales
dc.subjectPaleontología
dc.subjectMolecular characterization
dc.subjectSeed-fern ovule
dc.titleMolecular characterization of a seed-fern ovule (Pennsylvanian, Sydney Coalfield, Canada) by FTIR, <sup>13</sup>C NMR, and Py-GC-MS
dc.typeObjeto de conferencia
dc.typeResumen


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