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1.
Sources of sedimentary humic substances: vascular plant debris   总被引：1，自引：0，他引：1  
A modern Washington continental shelf sediment was fractionated densimetrically using either an organic solvent, CBrCl3, or aqueous ZnCl2. The resulting low density materials (<2.06 g/ml) account for only 1% of the sediment mass but contain 25% of the sedimentary organic carbon and 53% of the lignin. The C/N ratios (30–40) and lignin phenol yields (Λ = 8) and compositions indicate that the low density materials are essentially pure vascular plant debris which is slightly enriched in woody (versus nonwoody) tissues compared to the bulk sediment. The low density materials yield approximately one-third of their organic carbon as humic substances and contribute 23% and 14% of the total sedimentary humic and fulvic acids, respectively. Assuming that the lignin remaining in the sedimentary fraction is also contained in plant fragments that yield similar levels of humic substances, then 50% and 30% of the total humic and fulvic acids, respectively, arise directly from plant debris.Base-extraction of fresh and naturally degraded vascular plant materials reveals that significant levels of humic and fulvic acids are obtained using classical extraction techniques. Approximately 1–2% of the carbon from fresh woods and 10–25% from leaves and bark were isolated as humic acids and 2–4 times those levels as fulvic acids. A highly degraded hardwood yielded up to 44% of its carbon as humic and fulvic acids. The humic acids from fresh plants are generally enriched in lignin components relative to carbohydrates and recognizable biochemicals account for up to 50% of the total carbon. Humic and fulvic acids extracted directly from sedimentary plant debris could be responsible for a major fraction of the biochemical component of humic substances.  相似文献   

2.
Individual neutral sugars in sediments, sediment trap materials and major biological sources of a coastal marine environment (Dabob Bay, Washington State) were analyzed by capillary gas chromatography of equilibrated isomeric mixtures. Plankton, bacteria, and vascular plant tissues of different types yielded reproducible and biochemically consistent compositional patterns. These patterns, when expressed in simple parameters, allowed distinctions between marine and terrestrial carbohydrate sources as well as among the major different types of vascular plant tissues. Plankton and bacteria, due to their compositional diversity, were not further distinguishable by carbohydrate compositions alone. Carbohydrate compositions of Dabob Bay sediments and sediment trap materials, interpreted using source-indicator parameters, indicate a predominantly marine origin with increased relative input of terrestrially-derived carbohydrates in winter periods of low phytoplankton productivity. Both plankton and grasses are indicated as major carbohydrate sources during spring. Glucose yield enhancement factors, determined by comparative acid pretreatments, confirm the general predominance of α-cellulose-poor marine polysaccharides and increased levels of α-cellulose-rich vascular plant remains in winter sediment trap samples.  相似文献   

3.
The distribution and source of organic matter in reservoir sediments   总被引：2，自引：0，他引：2  
The bottom sediments of two reservoirs, one with significant river sediment input and one without, were analyzed for organic matter content. Lake Texoma sediments average 1.0% organic carbon, of which 0.26% organic carbon is deposited by the river sediments of the Red and Washita River deltas. In Fort Gibson reservoir, where there is minimal river sediment input, the organic carbon averages 1.2% and is deposited with a strong correlation to water depth (+0.9). There is a significant difference between the C/N ratio of Lake Texoma sediments (11.5) and Fort Gibson sediments (9.6). The higher C/N ratio is suggested to be a result of the larger input of terrestrial plant debris (with a high original C/N ratio) by the rivers draining into Lake Texoma and the relatively high resistance of the lignin material in the plant debris to decomposition in the reservoir sediments.  相似文献   

4.
The application of molecular approaches to palaeovegetation reconstruction in peat is still relatively rare, with molecular level studies of carbohydrate organic geochemistry being generally uncommon. In this report, neutral monosaccharides derived via acid hydrolysis were investigated in modern bog-forming plants in order to assess their potential application as biomarkers in peat palaeovegetation reconstruction. The concentrations of major neutral monosaccharides, i.e. glucose (Glu), xylose (Xyl), arabinose (Ara), galactose (Gal), mannose (Man), rhamnose (Rha) and fucose (Fuc), were determined using gas chromatography (GC) for 7 lichens, 10 Sphagnum species and 7 vascular plants collected from three ombrotrophic mires across northern Europe. Based on factor analysis of the modern plant monosaccharide compositions, two carbohydrate proxies: [(Man + Gal):(Ara + Xyl)] and % contributions of Rha and Fuc in total Glu-free monosaccharides [%(Rha + Fuc)], were selected as biomarkers for bog-forming plants. The three plant groups could be separated by [(Man + Gal):(Ara + Xyl)], which showed decreasing values following the order: lichens > Sphagna > vascular plants. The high [%(Rha + Fuc)] in Sphagna allowed their separation from lichens and vascular plants. These two factors were applied as plant group-specific indices to investigate vegetation change in a peat core from Kontolanrahka Bog, Finland. Our findings show strong correspondence with fossil plant abundances from the same core, thereby confirming the potential of carbohydrate compositional parameters as proxies for palaeovegetation reconstruction in peat bogs.  相似文献   

5.
A field study was conducted to clarify the effect of rhizosphere processes on the accumulation and partitioning of heavy metals (Pb, Zn, Cu, Cr, Cd and Ni) in mangrove sediments. Metals were fractionated by a sequential extraction procedure into three chemically distinct fractions: water soluble, exchangeable and carbonate bound (B1), Fe–Mn oxide bound (B2), and organic and sulfide bound (B3). Results indicate that rhizosphere processes tend to increase the metal concentrations in the rhizosphere sediments. However, plant uptake may result in the decrease of the metal concentrations in the rhizosphere sediments when the metal concentrations are relatively low in the bulk sediments. Compared with the bulk sediments, the rhizosphere sediments have low concentrations of heavy metals in the B1 and B2 fractions and high concentrations in the B3 fraction. Either an increase or decrease in the residual fraction of heavy metals in the rhizosphere sediments may appear, depending on whether the formation of the refractory metal-organic compounds or the activation of the residual fractions dominates. Results also indicate that mangrove plants absorb and store non-essential metals in the perennial tissues, thus reducing the export of non-essential metals via leaf litter transport. Mangrove plants are excellent candidates for phytostabilization of heavy metals in intertidal substrates.  相似文献   

6.
Vanillyl, syringyl and cinnamyl phenols occur as CuO oxidation products of humic, fulvic and base-insoluble residual fractions from soils, peat and nearshore marine sediments. However, none of these lignin-derived phenols were released by CuO oxidation of deepsea sediment or its base-extractable organic fractions. Lignin analysis indicated that peat and coastal marine sediments contained significantly higher levels of recognizable vascular plant carbon (20–50%) than soils and offshore marine sediments (0–10%).Although accounting for less than 20% of the total sedimentary (bulk) lignin, lignin components of humic acid fractions compositionally and quantitatively resembled the corresponding bulk samples and baseinsoluble residues. Recognizable lignin, presumably present as intact phenylpropanoid units, accounted for up to 5% of the carbon in peat and coastal humic acids but less than 1% in soil humic acids. Fulvic acid fractions uniformly yielded less lignin-derived phenols in mixtures that were depleted in syringyl and cinnamyl phenols relative to the corresponding humic acid fractions.Within the vanillyl and syringyl families the relative distribution of acidic and aldehydic phenols is a sensitive measure of the degree of oxidative alteration of the lignin component The high acid/aldehyde ratios and the low phenol yields of soils and their humic fractions compared to peat and coastal sediments indicate extensive degradation of the lignin source material. Likewise, the progressively higher acid/aldehyde ratios and lower phenol yields along the sequence: plant tissues (plant debris)-humic acids-fulvic acids suggest that this pattern represents the diagenetic sequence for the aerobic degradation of lignin biopolymers.  相似文献   

7.
The percentage composition and total amounts of fatty acids from plankton, live and dead plants (waterweeds and higher plants) and a forest soil, considered as possible origins of autochthonous and allochthonous organic materials in lacustrine sediments, have been determined by gas-liquid chromatography. Statistical analyses were carried out by computing distance index of the fatty acid composition between these source materials and the uppermost sediment from Lake Suwa, and the composition diversity index (CDI) of fatty acids in the recent sediments from Lake Suwa.The distance index indicated that the fatty acid composition in the uppermost sediment is similar to those in diatoms, Zooplankton and forest soil, and the values for dead leaves were smaller than for live ones. It suggests that the autolysis and/or decomposition processes prior to deposition onto the top sediment makes the fatty acid composition of organic debris similar to the uppermost sediment. The CPI in recent sediments varied irregularly, whereas the CDI increased during early diagenesis to yield a value comparable to ancient sediments.  相似文献   

8.
Aliphatic hydrocarbons, cupric oxide oxidation products of lignin and polycyclic aromatic hydrocarbons (PAH) were analyzed by capillary gas chromatography in sediments from the southern Washington continental shelf and slope. The concentration of diploptene relative to plantwax n-alkanes increased systematically in surface sediments with distance offshore along east-west transects of the study area and remained constant in surface sediments along the midshelf silt deposit. Analogous trends were also observed for the concentration of cinnamyl phenols relative to vanillyl phenols and total methylphenanthrenes relative to phenanthrene. These changes in sedimentary composition are evidence that diploptene from some terrestrial source, lignin characteristic of non-woody vascular plant tissue and a fossil organic material contained within weathered rock debris disperse across the Washington continental shelf and slope in geographic patterns distinct from that for other river-derived, chemically related materials. The compositional variations are explained by the particulate associations of the land-derived chemicals and differential hydraulic dispersion of their respective carrier particles after discharge at the mouth of the Columbia River.  相似文献   

9.
Cupric oxide oxidation has been employed to characterize the lignin geochemistry of Narragansett Bay sediments. Lignin concentrations throughout the estuary are low when expressed on a carbon-normalized basis, but can be characterized as enriched when expressed on a mass-normalized basis. This implies substantial dilution of the sedimentary lignin by inputs of lignin-poor carbon. Lignin concentrations do not correlate with the 13C isotopic composition of the sedimentary organic matter. These results are consistent with a sediment lignin component consisting of varying amounts of vascular plant debris and lignin-depleted organic matter, the latter originating from both marine (planktonic) and terrestrial (uncharacterized) sources. Compositional plots of lignin-derived phenols show that sediments in the upper estuary are influenced to a greater extent by gymnosperm lignin sources than those in the mid-and lower estuary. Given the extent to which the upper estuary is affected by pollution sources, inputs from anthropogenic discharges are the most likely cause of these compositional differences. However, an evaluation of processed paper products as an “anthropogenic” lignin source indicates that the lignin content of these materials is insufficient to account for the levels found in the sediments. Subsurface lignin compositions at an upper estuary site reveal that lignin originating from the inferred anthropogenic sources disappears at a depth shallower than that which would be expected based on the distribution of other trace organic pollutants (hydrocarbons and several synthetic organic compounds). We speculate that differences in either the depositional history or the degree of preservation of these two compound classes are responsible for the observed trends.  相似文献   

10.
Although recent research has indicated that bacteria may contribute an important fraction of biochemical residues in terrestrial and marine environments, it is difficult for geochemists to identify contributions from these ubiquitous and biochemically diverse organisms. Previous studies have suggested uronic acids and O-methyl sugars may be useful indicators of microbial abundance and activity, but have been limited primarily to analyses of a small number of isolated samples. We report here comparative distributions of O-methyl sugars, uronic acids, and aldoses in sediment trap material and sediments from Dabob Bay, WA and nearby Saanich Inlet, BC, where temporal and spatial trends may be used together with well-established patterns in other biochemicals to identify bacterial contributions against the background of other carbohydrate sources.O-methyl sugars and uronic acids were important contributors to the overall flux and burial of polysaccharide material in Dabob Bay and Saanich Inlet, composing ≤12 wt% of the total carbohydrate yields from sediment trap and sediment samples. O-methyl sugars accounted for an average of 5% of the carbohydrate yields from sediment trap materials and sediments, but were found rarely and only in low abundance in vascular plant tissues, phytoplankton, and kelp. In contrast, uronic acids were abundant products of sediment trap material and sediments, as well as vascular plant tissues, where in some cases they predominated among all carbohydrates. Uronic acid abundance in sediment trap material averaged 3% and ranged to >6% of total carbohydrate yields.The persistence of total minor sugar yields in water column collections from Dabob Bay throughout the seasonal cycle indicated they had a primary source that was not directly related to plankton bloom cycles nor pulsed inputs of vascular plant remains. Subsurface maxima in total minor sugar yields (and several individual components) within sediment cores from both sites indicate in situ sedimentary sources. Taken together, the observed environmental distributions strongly suggest that the minor sugar abundances in Dabob Bay and Saanich Inlet were controlled by in situ microbial production.  相似文献   

11.
Although rates and mechanisms of early diagenesis have been well studied, the effects of microbial metabolism on the molecular composition of the sedimentary organic matter (SOM) over long periods of time need more investigation. In this study, we characterize the early diagenesis of marine SOM from organic rich sediments of the Ocean Drilling Program site 1082 located off Namibia, in the vicinity of the Benguela coastal upwelling system. We used both Fourier transform infrared spectroscopy (FTIR) and nuclear magnetic resonance spectroscopy (13C NMR) to assess the quantitative partitioning of the organic carbon into major compound classes (aliphatic, aromatic, ester, carboxylic, amide and carbons from carbohydrates). Then, we calculate the SOM composition in the main biomolecules (proteins, carbohydrates, lipids and lignin) on the basis of previous 13C NMR based estimates of the molecular composition of the organic mixtures. Results show that the SOM is still labile at 7 m below the seafloor (mbsf) and composed of about 25% proteins and 15% carbohydrates. With increasing depth, the protein content exponentially decreases to 13% at 367 mbsf, whereas the carbohydrate content decreases linearly to 11%. The lignin and lipid content consistently represent around 10% and 40% of the SOM, respectively, and show an increase with depth, due mostly to selective enrichment as the more labile components are lost by degradation. Thus, these components of the SOM are considered refractory at the depth scale considered. The calculated remineralization rates are extremely slow ranging from 5.6 mol C m−3 ky−1 at the top of the core to 0.2 mol C m−3 ky−1 according to the organic carbon flux to the seafloor. Knowing the labile carbon losses, we propose a method to calculate the initial TOC before the diagenesis took place.  相似文献   

12.
Suspended sediments (SS) from the Atchafalaya River (AR) and the Mississippi River and surficial sediment samples from seven shallow cross-shelf transects west of the AR in the northern Gulf of Mexico were examined using elemental (%OC, C/N), isotopic (δ13C, Δ14C), and terrigenous biomarker analyses. The organic matter (OM) delivered by the AR is isotopically enriched (∼−24.5‰) and relatively degraded, suggesting that soil-derived OM with a C4 signature is the predominant OM source for these SS. The shelf sediments display OC values that generally decrease seaward within each transect and westward, parallel to the coastline. A strong terrigenous C/N (29) signal is observed in sediments deposited close to the mouth of the river, but values along the remainder of the shelf fall within a narrow range (8-13), with no apparent offshore trends. Depleted stable carbon isotope (δ13C) values typical of C3 plant debris (−27‰) are found near the river mouth and become more enriched (−22 to −21‰) offshore. The spatial distribution of lignin in shelf sediments mirrors that of OC, with high lignin yields found inshore relative to that found offshore (water depth > 10 m).The isotopic and biomarker data indicate that at least two types of terrigenous OM are deposited within the study area. Relatively undegraded, C3 plant debris is deposited close to the mouth of the AR, whereas more degraded, isotopically enriched, soil-derived OM appears to be deposited along the remainder of the shelf. An important input from marine carbon is found at the stations offshore from the 10-m isobath. Quantification of the terrigenous component of sedimentary OM is complicated by the heterogeneous composition of the terrigenous end-member. A three-end-member mixing model is therefore required to more accurately evaluate the sources of OM deposited in the study area. The results of the mixing calculation indicate that terrigenous OM (soil-derived OM and vascular plant debris) accounts for ∼79% of the OM deposited as inshore sediments and 66% of OM deposited as offshore sediments. Importantly, the abundance of terrigenous OM is 40% higher in inshore sediments and nearly 85% higher in offshore sediments than indicated by a two-end-member mixing model. Such a result highlights the need to reevaluate the inputs and cycling of soil-derived OM in the coastal ocean.  相似文献   

13.
Partitioning of carbon isotopes between main polymers of biomass of higher plants was investigated by the example of the structural polymers of wheat plant: lignin, hemicellulose, and cellulose representing the ligno-carbohydrate complex, starch and proteins representing storage compounds, and the lipid fraction. Biopolymers account from 80% (grasses) to 95% (trees) of the biomass of higher plants and are of geochemical interest as biological precursors for the terrigenous organic matter (OM) of sediments and sedimentary rocks. The biomass of algae is also dominated (∼80%) by polymers: proteins, carbohydrates, and lipids. The isotopic heterogeneity of the organs and parts of plants is controlled by carbon isotope composition (from −33.3 to −25.9‰) in biopolymers and their distribution: among various parts of plants. The carbohydrates: starch and hemicellulose are isotopically heaviest (−25.9 and −26.2‰), proteins are slightly poorer in 13C (up to −27.3‰), and lipids (−33.3‰) and lignin (−32.6‰) are isotopically light components of the biomass. The regularity of carbon isotopes partitioning among the large complexes of the biomass of higher plants is reflected in the existence of a common linear trend of δ13C values of biopolymers versus the ranges of thermodynamic β-factor values calculated by the method of isotopic bond numbers for the whole set of monomers in the composition of each polymer studied. The carbohydrates of grain and straw (starch, xylan, and cellulose) form a common C6–C5 pool of the isotopically heaviest polymers of the higher plant biomass (wheat). No significant isotopic effects were observed at the transformation between C6–C5 monomers and their transport between plant organs during grain ripening.  相似文献   

14.
New insights into the origin of perylene in geological samples   总被引：1，自引：0，他引：1  
The origin of the polycyclic aromatic hydrocarbon (PAH) perylene in sediments and petroleum has been a matter of continued debate. Reported to occur in Phanerozoic organic matter (OM), fossil crinoids and tropical termite mounds, its mechanism of formation remains unclear. While a combustion source can be excluded, structural similarities to perylene quinone-like components present in e.g. fungi, plants, crinoids and insects, potentially suggest a product-precursor relationship. Here, we report perylene concentrations, 13C/12C, and D/H ratios from a Holocene sediment profile from the Qingpu trench, Yangtze Delta region, China. Perylene concentrations differ from those of pyrogenic PAHs, and rise to prominence in a stratigraphic interval that was dominated by woody vegetation as determined by palynology including fungal spores. In this zone, perylene concentrations exhibit an inverse relationship to the lignin marker guaiacol, D/H ratios between −284‰ and −317‰, similar to the methoxy groups in lignin, as well as co-variation with spores from wood-degrading fungi. 13C/12C of perylene differs from that of land plant wax alkanes and falls in the fractionation range expected for saprophytic fungi that utilise lignin, which is isotopically lighter than cellulose and whole wood. During progressive lignin degradation, the relative carbon isotopic ratio of the perylene decreases. We therefore hypothesise a relationship of perylene to the activity of wood-degrading fungi. To support our hypothesis, we analysed a wide range of Phanerozoic sediments and oils, and found perylene to generally be present in subordinate amounts before the evolutionary rise of vascular plants, and to be generally absent from marine-sourced oils, few exceptions being attributed perhaps to a contribution of marine and/or terrestrial-derived fungi, anoxia (especially under marine conditions) and/or contamination of core material by fungi. A series of low-molecular-weight aromatic quinones bearing the perylene-backbone were detected in Devonian and Cretaceous sediments, potentially representing precursor components to perylene.  相似文献   

15.
The high molecular weight fraction of dissolved organic matter in a suite of lakes, rivers, seawater, and marine sediment interstitial water samples was collected by ultrafiltration and characterized by molecular level and spectroscopic techniques. Proton nuclear magnetic resonance spectra of all samples show a high degree of similarity, with major contributions from carbohydrates, bound acetate, and lipids. Molecular level analyses of neutral sugars show seven monosaccharides, rhamnose, fucose, arabinose, xylose, mannose, glucose, and galactose, to be abundant, and to occur in comparable relative amounts in each sample. Previous studies have emphasized the distinctive composition of dissolved humic substances in fresh and marine waters, and have attributed these differences to sources and transformations of organic matter unique to each environment. In contrast we find a large fraction of freshwater high molecular weight dissolved organic matter (HMWDOM; > 1kD) to be indistinguishable from marine HMWDOM in bulk and molecular-level chemical properties. Aquatic HMWDOM is similar in chemical composition to biologically derived acylated heteropolysaccharides isolated from marine algal cultures, suggesting a biological source for some fraction of persistent HMWDOM. High molecular weight DOC contributes 51 ± 26% of the total DOC, and monosaccharides 18 ± 8% of the total HMWDOC in our freshwater samples. These contributions are on average higher and more variable, but not significantly different than for surface seawater (30% and 16% respectively). Biogeochemical processes that produce, accumulate, and recycle DOM may therefore share important similarities and be broadly comparable across a range of environmental settings.  相似文献   

16.
Microbial contributions to the detritus of two vascular plant tissues, smooth cordgrass (Spartina alterniflora) and black mangrove leaves (Avicennia germinans), were estimated over a 4-year decomposition period under subaqueous marine conditions. During this period, 93-97% of the initial plant tissues was decomposed. Bulk elemental and isotopic compositions of the detritus were measured along with hydrolyzable amino sugars (AS) and amino acids (AA), including the bacterial biomarkers muramic acid and the d-enantiomers of AA. A major enrichment in N relative to C occurred during decomposition. Net increases of AS, AA, and bacterial biomarkers in decaying detritus were observed. Three independent approaches indicated that on average 60-75% of the N and 20-40% of the C in highly decomposed detritus were not from the original plant tissues but were mostly from heterotrophic bacteria. During decomposition hydrolyzable AS + AA yields (∼54% of total N) were strongly correlated with total N in both types of detritus. The uncharacterized N appeared to have the same origin and dynamics as AA, suggesting the contribution of other bacterial biomolecules not measured here. There was little indication of humification or abiotic processes. Instead, N-immobilization appeared primarily bacterially mediated. Although varying dynamics were observed among individual molecules, bacterial detritus exhibited an average reactivity similar to plant detritus. Only a minor fraction of the bacterial detritus escaped rapid biodegradation and the relationship between bacterial activity and N-immobilization is consistent with an enzymatically mediated preservation mechanism. Bacteria and their remains are ubiquitous in all ecosystems and thus could comprise a major fraction of the preserved and uncharacterized organic matter in the environment.  相似文献   

17.
Lignin oxidation products and 13C/12C ratios were compared as indicators of land-derived organic matter in surface sediments from the western Gulf of Mexico. Whole sediments were reacted with cupric oxide to yield phenolic oxidation products that indicated the types and relative amounts of the lignins that were present.Measurements of lignin concentration and carbon isotope abundances both indicated a sharp offshore decrease of land-derived organic matter in most areas of the western Gulf. This decrease results primarily from mixing of terrestrial and marine organic matter. The terrestrially derived material in these sediments has a lignin content similar to that of grasses and tree leaves. Flowering plants contribute most of the sedimented lignin compounds. These lignins apparently occur in the form of well-mixed plant fragments that are transported to sea by rivers and deposited primarily on the inner continental shelf.  相似文献   

18.
Isotopic and elemental analysis, Fourier transform infrared spectroscopy (FTIR), principal components analysis (PCA) and two dimensional (2D) correlation analysis, where core depth was used as perturbation, were used to study the diagenesis of organic matter (OM) in Lake Superior sediments. Changes in OM composition were examined at five lake stations over a depth range of 0–10 cm. PCA results show that depth-related changes among sites are similar, leading to an increased contribution from inorganic (and possibly refractory aromatic organic) components at each site, and a loss of contribution from other organic components. Synchronous spectra reveal that aliphatic esters and carbohydrates are degraded significantly with increasing depth, leading to an increased contribution from clay/biogenic silica/inactive carbohydrates. Asynchronous spectra show that, in general, carboxyl groups, including aliphatic ester and amide in protein, are degraded first, followed by a group of carbohydrates and then aromatic compounds and/or the SiO framework in clay and biogenic silica. Site dependent compositional variation occurs and appears to be influenced by topography and geology, e.g. the delivery of a larger load of terrestrial inorganic silicate minerals to certain sites and re-suspension/re-deposition, leading to less intensive down core variation at mid-lake central and eastern basin sites. The study demonstrates the usefulness of FTIR coupled with PCA and 2D correlation approaches for exploring structural changes in sedimentary material during diagenesis.  相似文献   

19.
This paper describes simulation experiments in which glucose and cellulose were reacted with polysulphide and hydrogen sulphide at ambient temperatures in an aqueous environment. Organic sulphur containing compounds were formed that yield several thiophenes upon pyrolysis/evaporation. The experiments show that interaction of carbohydrates with hydrogen sulphide or polysulphides is a possible way for carbohydrates to react in very recent sediments. From the results of this study it can be concluded that carbohydrate carbon can be preserved in sediments in a form that is resistant to microbial attack and that will have a greater potential for survival during diagenesis than the carbohydrate precursor.  相似文献   

20.
Vegetative remains of three coalified Lower Devonian vascular plants (Zosterophyllum, Psilophyton, Renalia) were analyzed using flash pyrolysis-gas chromatography-mass spectrometry. The distributions of pyrolysis products are compared with those from younger vascular plant fossil xylem (Cordaixylon, Callixylon) and cuticle (Pachypteris). The likelihood of the chemical preservation of characteristic higher plant macromolecules (e.g., lignin and cutan) in the Lower Devonian plant fossils is considered in light of this comparison and associated thermal maturity assessments. Reflectance values from vitrinite-like macerals, which may not be vitrinite sensu stricto in the Lower Devonian host rocks for the fossils selected for this study, are shown to provide a reasonable assessment of the thermal maturity of these early vascular plant fossils. Although lignin altered through burial maturation is the most likely source of the prominent alkylphenols and aromatic hydrocarbons in the Lower Devonian tracheophyte flash pyrolysates, a contribution from thermally modified tannins cannot be ruled out. Comparison of the highly aliphatic pyrolysates from the Zosterophyllum and Psilophyton axes with that of a thermally mature fossil gymnosperm leaf revealed that cutan was an important component in the Devonian plant remains. This is the earliest chemical evidence for the presence of cutan in vascular plants.  相似文献   

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