Structural modification of lignin in peat during peat formation at tropical swamp

Peat samples from typical tropical peat swamp around Narathiwat Province, southern Thailand, were collected from various depths of peat profile (from surface to 210 cm depth), of which dates were established using an accelerator mass spectrometry from 0 to 2600 years BP. The samples were analysed to...

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Veröffentlicht in:JARQ. Japan agricultural research quarterly 2009, Vol.43(1), pp.71-79
Hauptverfasser: Jin, Z.(Tokyo Univ. (Japan)), Shao, S, Katsumata, K.S, Ishida, T, Iiyama, K
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Shao, S
Katsumata, K.S
Ishida, T
Iiyama, K
description Peat samples from typical tropical peat swamp around Narathiwat Province, southern Thailand, were collected from various depths of peat profile (from surface to 210 cm depth), of which dates were established using an accelerator mass spectrometry from 0 to 2600 years BP. The samples were analysed to discuss changes in structural characteristics of lignin in peat samples during peat formation. The samples were fractionated based on pH adjustment into dilute alkali soluble (ALsub(sol)) and insoluble (ALsub(insol)) fractions. Only glucosyl and xylosyl residues were detected in ALsub(insol) fraction, but no monosaccharide in ALsub(sol) fraction. Lignin contents of ALsub(insol) fraction of the peat samples ranged from 73.0 to 83.3%. Lignin was significantly modified during peat formation. The progress of condensation reactions, introduction of carboxyl groups and partially loss of methoxyl groups, cleavage of arylglycerol- beta-aryl ether linkage, were confirmed by alkaline nitrobenzene oxidation, functional group analysis and analytical ozonation, respectively, due to the microbial activities. Lignin of the peat samples was isolated by Bjoerkman's procedure to discuss structural feature in detail using spectrometrical procedures as the first trial in the field of geochemistry. The signals around 6.6 and 6.9 ppm in sup(1)H-NMR were considerably weak compare with those of lignin from fresh wood, suggesting high condensation. The most peaks originating from lignin of fresh wood were also detected in the FTIR spectrum. The ionization difference (deltaEsub(i)) spectrum clearly showed the presence of unconjugated and conjugated phenolic hydroxyl groups. Thus, lignin in peat was modified significantly by microbial activities. It is expected that further modified fragments of lignin would be soluble in water and flow-out to ocean through rivers.
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The progress of condensation reactions, introduction of carboxyl groups and partially loss of methoxyl groups, cleavage of arylglycerol- beta-aryl ether linkage, were confirmed by alkaline nitrobenzene oxidation, functional group analysis and analytical ozonation, respectively, due to the microbial activities. Lignin of the peat samples was isolated by Bjoerkman's procedure to discuss structural feature in detail using spectrometrical procedures as the first trial in the field of geochemistry. The signals around 6.6 and 6.9 ppm in sup(1)H-NMR were considerably weak compare with those of lignin from fresh wood, suggesting high condensation. The most peaks originating from lignin of fresh wood were also detected in the FTIR spectrum. The ionization difference (deltaEsub(i)) spectrum clearly showed the presence of unconjugated and conjugated phenolic hydroxyl groups. Thus, lignin in peat was modified significantly by microbial activities. 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Only glucosyl and xylosyl residues were detected in ALsub(insol) fraction, but no monosaccharide in ALsub(sol) fraction. Lignin contents of ALsub(insol) fraction of the peat samples ranged from 73.0 to 83.3%. Lignin was significantly modified during peat formation. The progress of condensation reactions, introduction of carboxyl groups and partially loss of methoxyl groups, cleavage of arylglycerol- beta-aryl ether linkage, were confirmed by alkaline nitrobenzene oxidation, functional group analysis and analytical ozonation, respectively, due to the microbial activities. Lignin of the peat samples was isolated by Bjoerkman's procedure to discuss structural feature in detail using spectrometrical procedures as the first trial in the field of geochemistry. The signals around 6.6 and 6.9 ppm in sup(1)H-NMR were considerably weak compare with those of lignin from fresh wood, suggesting high condensation. The most peaks originating from lignin of fresh wood were also detected in the FTIR spectrum. The ionization difference (deltaEsub(i)) spectrum clearly showed the presence of unconjugated and conjugated phenolic hydroxyl groups. Thus, lignin in peat was modified significantly by microbial activities. 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Japan agricultural research quarterly</jtitle><addtitle>JARQ</addtitle><date>2009-01</date><risdate>2009</risdate><volume>43</volume><issue>1</issue><spage>71</spage><epage>79</epage><pages>71-79</pages><issn>0021-3551</issn><eissn>2185-8896</eissn><abstract>Peat samples from typical tropical peat swamp around Narathiwat Province, southern Thailand, were collected from various depths of peat profile (from surface to 210 cm depth), of which dates were established using an accelerator mass spectrometry from 0 to 2600 years BP. The samples were analysed to discuss changes in structural characteristics of lignin in peat samples during peat formation. The samples were fractionated based on pH adjustment into dilute alkali soluble (ALsub(sol)) and insoluble (ALsub(insol)) fractions. Only glucosyl and xylosyl residues were detected in ALsub(insol) fraction, but no monosaccharide in ALsub(sol) fraction. Lignin contents of ALsub(insol) fraction of the peat samples ranged from 73.0 to 83.3%. Lignin was significantly modified during peat formation. The progress of condensation reactions, introduction of carboxyl groups and partially loss of methoxyl groups, cleavage of arylglycerol- beta-aryl ether linkage, were confirmed by alkaline nitrobenzene oxidation, functional group analysis and analytical ozonation, respectively, due to the microbial activities. Lignin of the peat samples was isolated by Bjoerkman's procedure to discuss structural feature in detail using spectrometrical procedures as the first trial in the field of geochemistry. The signals around 6.6 and 6.9 ppm in sup(1)H-NMR were considerably weak compare with those of lignin from fresh wood, suggesting high condensation. The most peaks originating from lignin of fresh wood were also detected in the FTIR spectrum. The ionization difference (deltaEsub(i)) spectrum clearly showed the presence of unconjugated and conjugated phenolic hydroxyl groups. 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subjects analytical ozonation
arylglycerol-β-aryl ether linkage
ASIA TROPICAL
ASIE TROPICALE
biological modification of lignin
BIOMASA
BIOMASS
BIOMASSE
CARBOHYDRATE CONTENT
CONTENIDO DE CARBOHIDRATOS
LIGNINAS
LIGNINE
LIGNINS
PEAT
TENEUR EN GLUCIDES
TOURBE
TROPICAL ASIA
TURBA
title Structural modification of lignin in peat during peat formation at tropical swamp
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