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Evolution of the macromolecular structure of sporopollenin during thermal degradation

Reconstructing the original biogeochemistry of organic microfossils requires quantifying the extent of the chemical transformations they experienced during burial and maturation processes. In the present study, fossilization experiments have been performed using modern sporopollenin chosen as an ana...

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Autores principales: Bernard, S., Benzerara, K., Beyssac, O., Balan, E., Brown Jr., G.E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4832518/
https://www.ncbi.nlm.nih.gov/pubmed/27123494
http://dx.doi.org/10.1016/j.heliyon.2015.e00034
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author Bernard, S.
Benzerara, K.
Beyssac, O.
Balan, E.
Brown Jr., G.E.
author_facet Bernard, S.
Benzerara, K.
Beyssac, O.
Balan, E.
Brown Jr., G.E.
author_sort Bernard, S.
collection PubMed
description Reconstructing the original biogeochemistry of organic microfossils requires quantifying the extent of the chemical transformations they experienced during burial and maturation processes. In the present study, fossilization experiments have been performed using modern sporopollenin chosen as an analogue for the resistant biocompounds possibly constituting the wall of many organic microfossils. Sporopollenin powder has been processed thermally under argon atmosphere at different temperatures (up to 1000 °C) for varying durations (up to 900 min). Solid residues of each experiment have been characterized using infrared, Raman and synchrotron-based XANES spectroscopies. Results indicate that significant defunctionalisation and aromatization affect the molecular structure of sporopollenin with increasing temperature. Two distinct stages of evolution with temperature are observed: in a first stage, sporopollenin experiences dehydrogenation and deoxygenation simultaneously (below 500 °C); in a second stage (above 500 °C) an increasing concentration in aromatic groups and a lateral growth of aromatic layers are observed. With increasing heating duration (up to 900 min) at a constant temperature (360 °C), oxygen is progressively lost and conjugated carbon–carbon chains or domains grow progressively, following a log-linear kinetic behavior. Based on the comparison with natural spores fossilized within metasediments which experienced intense metamorphism, we show that the present experimental simulations may not perfectly mimic natural diagenesis and metamorphism. Yet, performing such laboratory experiments provides key insights on the processes transforming biogenic molecules into molecular fossils.
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spelling pubmed-48325182016-04-25 Evolution of the macromolecular structure of sporopollenin during thermal degradation Bernard, S. Benzerara, K. Beyssac, O. Balan, E. Brown Jr., G.E. Heliyon Article Reconstructing the original biogeochemistry of organic microfossils requires quantifying the extent of the chemical transformations they experienced during burial and maturation processes. In the present study, fossilization experiments have been performed using modern sporopollenin chosen as an analogue for the resistant biocompounds possibly constituting the wall of many organic microfossils. Sporopollenin powder has been processed thermally under argon atmosphere at different temperatures (up to 1000 °C) for varying durations (up to 900 min). Solid residues of each experiment have been characterized using infrared, Raman and synchrotron-based XANES spectroscopies. Results indicate that significant defunctionalisation and aromatization affect the molecular structure of sporopollenin with increasing temperature. Two distinct stages of evolution with temperature are observed: in a first stage, sporopollenin experiences dehydrogenation and deoxygenation simultaneously (below 500 °C); in a second stage (above 500 °C) an increasing concentration in aromatic groups and a lateral growth of aromatic layers are observed. With increasing heating duration (up to 900 min) at a constant temperature (360 °C), oxygen is progressively lost and conjugated carbon–carbon chains or domains grow progressively, following a log-linear kinetic behavior. Based on the comparison with natural spores fossilized within metasediments which experienced intense metamorphism, we show that the present experimental simulations may not perfectly mimic natural diagenesis and metamorphism. Yet, performing such laboratory experiments provides key insights on the processes transforming biogenic molecules into molecular fossils. Elsevier 2015-10-26 /pmc/articles/PMC4832518/ /pubmed/27123494 http://dx.doi.org/10.1016/j.heliyon.2015.e00034 Text en © 2015 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Bernard, S.
Benzerara, K.
Beyssac, O.
Balan, E.
Brown Jr., G.E.
Evolution of the macromolecular structure of sporopollenin during thermal degradation
title Evolution of the macromolecular structure of sporopollenin during thermal degradation
title_full Evolution of the macromolecular structure of sporopollenin during thermal degradation
title_fullStr Evolution of the macromolecular structure of sporopollenin during thermal degradation
title_full_unstemmed Evolution of the macromolecular structure of sporopollenin during thermal degradation
title_short Evolution of the macromolecular structure of sporopollenin during thermal degradation
title_sort evolution of the macromolecular structure of sporopollenin during thermal degradation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4832518/
https://www.ncbi.nlm.nih.gov/pubmed/27123494
http://dx.doi.org/10.1016/j.heliyon.2015.e00034
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