A possible chlorophycean affinity of some Neoproterozoic acritarchs

Two taxa of Neoproterozoic acritarchs of unknown affinity, Multifronsphaeridium pelorium and Species A, are analysed by electron microscopic (SEM, TEM) and chemical (micro-FTIR, pyrolysis GC–MS, thermal desorption–MS) methods. Both acritarch species are characterised by multi-branched processes and...

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Veröffentlicht in:Organic geochemistry 1999-01, Vol.30 (10), p.1323-1337
Hauptverfasser: Arouri, Khaled, Greenwood, Paul F, Walter, Malcolm R
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Walter, Malcolm R
description Two taxa of Neoproterozoic acritarchs of unknown affinity, Multifronsphaeridium pelorium and Species A, are analysed by electron microscopic (SEM, TEM) and chemical (micro-FTIR, pyrolysis GC–MS, thermal desorption–MS) methods. Both acritarch species are characterised by multi-branched processes and a remnant trilaminar sheath (TLS) structure. The TLS-bearing wall structures in these acritarchs suggest a possible biological affinity to chlorophyte algaenan. The molecular data obtained from the two acritarchs were generally similar and also consistent with a chlorophycean affinity. A significant aliphatic moiety is evident in these acritarchs as a short-chain series of n-alkene/alkane pyrolysates and prominent aliphatic IR bands. The restricted molecular-weight range (
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Both acritarch species are characterised by multi-branched processes and a remnant trilaminar sheath (TLS) structure. The TLS-bearing wall structures in these acritarchs suggest a possible biological affinity to chlorophyte algaenan. The molecular data obtained from the two acritarchs were generally similar and also consistent with a chlorophycean affinity. A significant aliphatic moiety is evident in these acritarchs as a short-chain series of n-alkene/alkane pyrolysates and prominent aliphatic IR bands. The restricted molecular-weight range (&lt;C 20) of the n-alkene/alkane doublets and the lack of isoprenoid and other branched alkanes in the pyrolysates suggest a low degree of branching in the aliphatic component of these acritarch macromolecules. The significant methyl (CH 3) IR signal was attributed to the terminal groups of short n-alkyl moieties. Alkylbenzenes, alkylphenols and alkylindoles were also significant pyrolysis products, indicating an aromatic component, although the latter two components may be attributed to artificially- and/or diagenetically-formed melanoidin moieties. The macromolecular structure of Multifronsphaeridium sp. and Species A consists of short n-alkylpolymethylenic chains, probably linked via ether/ester bonds, with possibly a small aromatic content. 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Both acritarch species are characterised by multi-branched processes and a remnant trilaminar sheath (TLS) structure. The TLS-bearing wall structures in these acritarchs suggest a possible biological affinity to chlorophyte algaenan. The molecular data obtained from the two acritarchs were generally similar and also consistent with a chlorophycean affinity. A significant aliphatic moiety is evident in these acritarchs as a short-chain series of n-alkene/alkane pyrolysates and prominent aliphatic IR bands. The restricted molecular-weight range (&lt;C 20) of the n-alkene/alkane doublets and the lack of isoprenoid and other branched alkanes in the pyrolysates suggest a low degree of branching in the aliphatic component of these acritarch macromolecules. The significant methyl (CH 3) IR signal was attributed to the terminal groups of short n-alkyl moieties. Alkylbenzenes, alkylphenols and alkylindoles were also significant pyrolysis products, indicating an aromatic component, although the latter two components may be attributed to artificially- and/or diagenetically-formed melanoidin moieties. The macromolecular structure of Multifronsphaeridium sp. and Species A consists of short n-alkylpolymethylenic chains, probably linked via ether/ester bonds, with possibly a small aromatic content. 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Both acritarch species are characterised by multi-branched processes and a remnant trilaminar sheath (TLS) structure. The TLS-bearing wall structures in these acritarchs suggest a possible biological affinity to chlorophyte algaenan. The molecular data obtained from the two acritarchs were generally similar and also consistent with a chlorophycean affinity. A significant aliphatic moiety is evident in these acritarchs as a short-chain series of n-alkene/alkane pyrolysates and prominent aliphatic IR bands. The restricted molecular-weight range (&lt;C 20) of the n-alkene/alkane doublets and the lack of isoprenoid and other branched alkanes in the pyrolysates suggest a low degree of branching in the aliphatic component of these acritarch macromolecules. The significant methyl (CH 3) IR signal was attributed to the terminal groups of short n-alkyl moieties. 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subjects Algae
Algaenan
Aromatic compounds
Chlorophyceae
Earth sciences
Earth, ocean, space
Electron microscopy
Exact sciences and technology
Fourier transform infrared spectroscopy
Laser micropyrolysis GC–MS
Macromolecules
Micro-FTIR
Molecular weight
Neoproterozoic acritarchs
Olefins
Paleobotany
Paleontology
Paraffins
Pyrolysis
Stratigraphy
Thermal desorption–MS
Trilaminar sheath cell walls
title A possible chlorophycean affinity of some Neoproterozoic acritarchs
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