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1.
Detailed geochemical analyses of the high reduction zone in Lake Suwa sediments suggested that the stenol to stanol conversion rate in this zone is primarily controlled by the proportion of autochthonous contribution to organic matter and the redox potential in these sediments, and that land-derived stenols were kept insensitive to hydrogenation in lacustrine sediments as compared with those derived from plankton. These results indicate that stanols derived directly from organisms on land may contribute significantly to stanols found in lacustrine sediments which contain minor proportions of autochthonous organic materials.In order to express the relative autochthonous vs terrigenous contribution to organic matter in lacustrine sediments, the autochthonous contribution index (ACI) was defined based on the characteristic distribution of sterol in plankton and land plants. It systematically increased from river inlet towards lake center and correlated closely with the δ13C value in same sediments. This strongly indicates that ACI is a useful indicator providing informatiom on autochthonous vs terrigenous contribution to the organic material in lacustrine sediments.  相似文献   

2.
Significant quantities of solvent-inextractable geolipids, obtained by saponification of solvent extracted sediments, were found in various sedimentary samples including soils, river inlet sediment and lake sediments from Lake Suwa.The carbon isotopic composition (δ13C) of extractable and inextractable geolipids from the same sediment sample were similar. Moreover, the carbon number distributions of sterols in the two geolipid fractions from the same sediment were also similar.Whereas the ratios of both lipids and sterols to total organic carbon for the extractable geolipids in the lake sediments decreased with depth, the former ratio for inextractable giolipids tends to increase with depth and the latter remains fairly constant. On the other hand, the stanol to stenol ratio of the extractable fraction increased with depth but that of the inextractable fraction was lower than that of the extractable fraction and was fairly constant irrespective of sediment depth.The transformation of extractable sterols into inextractable ones was not observed during incubation for 1200 days of sterols with Suwa sediments.Thus, the following conclusions were made: (1) the extractable and inextractable geolipids have similar origins, (2) some constituents of the latter may be protected from chemical or microbiological degradation and transformation in the sediments, and (3) the transformation of some constituents of the former into the inextractable ones virtually does not occur after incorporation into Suwa sediments.These results suggest that some constituents of the inextractable geolipid fraction may provide fundamental information on early diagenetic alteration of geolipids in lake sediments and on the relatively recent paleoenvironment.  相似文献   

3.
青海湖沉积物中的甾醇及其演化   总被引：3，自引：0，他引：3  
Ｃ２７，Ｃ２８和Ｃ２９甾醇（△５.２２，△２２，△５和△５.２４（２８）和５α－甾烷醇）在青海湖三孔近代沉积物（ＱＨ，ＱＥ和ＱＯ）中被检出。其中以Ｃ２９甾醇占优势。在ＱＥ和ＱＧ孔沉积物中还检出了低浓度的三个Ｃ３０甾醇（４α，２３，２４－三甲基－５α－胆甾－２２Ｅ－烯醇（甲藻甾醇），４α－甲基－２４－乙基－５α－胆甾－２２Ｅ－烯醇和４α－甲基－２４－乙基－５α－胆甾烷醇］。在ＱＨ和ＱＧ孔上部层段沉积物中，Ｃ２７，Ｃ２９.饱和的和不饱和的甾醇的碳数分布的平行性，甾烷醇/△５－甾醇及△２２－/△５.２２－甾醇的比值随沉积物埋深而增加提供了甾酸氢化作用的间接证据。青海湖沉积物中的甾醇主要来自湖区丰富的高等植物和湖中的藻类等。在ＱＧ孔８０～１００ｃｍ和１２０～１４０ｃｍ层段沉积物中，５ａ－胆甾烷醇浓度迅速增加可能反映特殊的生物（介形类）对该二层段沉积物中高浓度的胆甾烷醇的贡献。  相似文献   

4.
Water samples collected from a slope station and two deep stations in the western basin of the Black Sea were analyzed for stenols and stanols by glass capillary gas chromatography. These results were used in conjuction with hydrographic, particulate organic carbon, and chlorophyll a data to better understand sterol sources and their transport and transformation mechanisms in anoxic basins.The total free sterol concentrations found in the surface waters were 450–500 ng/l dropping rapidly to values well below 100 ng/l at depths below the O2H2S interface. In the upper 200 m of the water column a strong association of sterols with particulate matter is suggested. Structural elucidation by a gas chromatograph-mass spectrometer-computer system revealed the presence of at least sixteen different stenols and stanols in the surface waters of the Black Sea. Cholesterol, 24-methylenecholesterol and 24-methylcholesta-5,22-dien-3β-ol were the major sterols in the surface waters. Cholesterol and 24-ethylcholesterol both exhibited a subsurface maximum at the O2H2S interface. In the anoxic deep waters (200–2000 m) only cholesterol and 24-ethylcholesterol were found. Two stenols were found that have not been reported in seawater: a C26 stenol with a saturated C7H15 side chain (presumably 24-norcholesterol) and 24-ketocholesterol. At least six 5α-stanols could be identified in the surface samples, each of them comprising about 10–20% of the concentration of the corresponding Δ5-stenol. From these comparatively high surface values the stanol concentrations drop rapidly to values near zero at the O2H2S interface. Except for very low concentrations of 5α-cholestanol (< 4ng/l) no other stanols could be detected in the anoxic zone.From this data it appears that no detectable stenol → stanol conversion is occurring at the O2H2S interface or in the deep anoxic waters of the Black Sea.  相似文献   

5.
A 3-m sediment core taken from Lake Suigetsu, in which a shift from fresh to brackish water occurred about three hundred years ago, has been examined for variation with depth of organic carbon and fatty acids. From the difference in total amounts of sulphur between sediments under fresh and brackish water environments, the surface sediments above approximately 35 cm depth were deduced to be accumulated under a brackish water environment. The total contents of organic carbon and fatty acids, and percentage composition of fatty acids gave discontinuous profiles above and below the 35–40 cm sediment layer. At a depth of 12.5 cm, the distribution in chain length of the fatty acids changed from a unimodal (the predominance of C12-C18 over C20-C34) to a bimodal pattern, which was mirrored by the composition diversity index (CDI).Although the fatty acids in the surface sediments (0–40 cm) from Lake Suigetsu seemed to suffer milder degradation through microbial activity than those in a core (0–150 cm) from Lake Suwa, a freshwater eutrophic lake, both lacustrine sediments showed similar trends in the alteration of fatty acid composition with depth.  相似文献   

6.
Organic molecules originating only from the in situ diagenesis of biogenic molecules are ideal geochemical fossils which may provide information essential for the characterization and reconstruction of depositional environments and subsequent chemical reactions during diagenesis. It is proposed herein that this is the case for the 5β-isomers of stanols and stanones produced during stenol hydrogenation in young aquatic sediments, if shown to be essentially free of any major anthropogenic pollution (particularly, sewage). In order to clarify the environmental factors controlling the production of the 5β-steroidal isomers from stenols in recent aquatic sediments, attempts were made to relate the occurrence of 5β-stanols to various environmental parameters. Positive correlations between elevated concentrations of 5β-stanols and the degree of autochthonous contribution to sedimentary organic matter were consistently found in various surface aquatic sediments from a wide variety of depositional environments and also in older sediments extending even to the late Pleistocene. According to this finding, it was concluded that the primary factor controlling the conversion of stenols to 5β-stanols through 5β-stanones in anaerobic aquatic sediments is probably the relative contribution of autochthonous organic matter suitable for microbial metabolism (i.e. metabolizable organic matter) to the sediments. Consequently, it is proposed that the 5β-isomers of stanols and stanones, at least in immature aquatic (marine and non-marine) sediments, can serve as primary markers for defining the quality of sedimentary organic matter (viz. the relative contribution of metabolizable organic materials to sedimentary organic matter) and as indicators for the types and rates of microbiological activities responsible for early diagenesis of organic matter in anaerobic sediments. It is also suggested that the combination of the 5β-steroidal isomers with organic source parameters will allow these compounds to assist in indicating oxic or anoxic depositional environments.  相似文献   

7.
The distributions of free 4-desmethyl sterols in sediments from the Peru coastal zone at 15°S have been determined. Major free sterols in the surface sediments include cholesterol, which is mainly derived from zooplankton, and two C28 sterols: 24-methylcholesta-5,24(28)-dien-3β-ol and 24-methylcholesta-5,22E-dien-3β-ol both of which are derived fro diatoms. Their concentrations decrease by almost an order of magnitude in the top 20 cm of sediment depth, indicating that free sterols are rapidly degraded in this sedimentary environment. Lipids from higher plants were also detected: long chain fatty acids and alcohols and various triterpenoid alcohols, including taraxerol, lupeol and α- and β-amyrin. The concentrations of most terrigenous lipids varied by less than a factor of 3 over the same depth, and these changes were not correlated with changes in the concentrations of total organic carbon. Below 3 cm, lipids from higher plants predominated in the extractable lipid distributions due to the more rapid degradation of marine lipids. We postulate that there are significant marine sources of the higher plant sterols 24-ethylcholesterol, 24-ethylcholesta-5,22E-dien-3β-ol and 24-methylcholesterol in these sediments. A high proportion of many of the terrigenous lipids in these sediments are probably transported into the coastal zone by rivers, rather than from the atmosphere, and then redistributed by bottom currents.  相似文献   

8.
The extractable organic matter of sediment samples from six sampling sites in Lake Perdana, Kuala Lumpur, was analyzed to characterize the source inputs. The analysis of aliphatic homologous series indicated that terrestrial higher plant waxes can be assigned as the major sources of the identified aliphatic components in the lake sediments. The presence of an unresolved complex mixture of branched and cyclic compounds and a series of hopanes ranging from C27 to C35 reflected the contamination by petroleum residues from urban vehicular emissions brought in by runoff and fallout. The steroids present included stenols and stanols and showed an input of organic matter from higher plants. The detected pentacyclic triterpenoids comprised oleanane, ursane, lupane and friedelane skeletons including unsaturated oxygenated, mono-, di- and triaromatic counterparts. They are recognized as biomarkers for angiosperms. The presence of des-A-triterpenoids and their aromatized derivatives as the major diagenetic products of triterpenoids reflected the degradation of natural organic matter in the sediments occurring under mainly anoxic conditions. In addition, the presence of tetrahymanol and ββ-bishomohopan-32-ol indicated a minor algal/plankton and bacterial input to the sediments.  相似文献   

9.
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   

10.
In order to attempt to elucidate the nature of biogeochemical processes occurring at the water-sediment interface, sterols have been analysed in near bottom sea and interstitial waters collected in the eastern and western intertropical Atlantic ocean. Free and esterified sterol concentrations range from 0.2 to 82 μg l?1 and are much higher than those found in overlying sea water, which range from 0.2 to 1.7 μg l?1 for the dissolved fraction and from 0.01 to 0.07 μg l?1 for the particulate fraction. Cholest-5-en-3β-ol and 24-ethylcholest-5-en-3β-ol are the dominant sterols in sea and interstitial waters. The variability encountered for the relative importance of minor sterols such as 24-methylcholesta-5,24(28)-dien-3β-ol and stanols, 5α-cholest-22(E)-en-3β-ol, 5α-cholestan-3β-ol and 24-ethyl-5α-cholestan-3β-ol in interstitial water and their variation with depth is discussed in terms of diversity of inputs and bacterial activity. For sediments cored off the Mauritanian coast, a productive area characterized by an intense upwelling, the chemical signatures observed in interstitial water through stanol/stenol ratios occur at levels of very high heterotrophic aerobic bacterial biomass estimations. The study of the sterol composition of interstitial water could constitute a valuable tool in appreciating the intensity of chemical and biological processes occurring in the first few metres of recent marine sediments.  相似文献   

11.
Detailed compositional data for the sterols isolated from a surface, Unit I, sediment from the Black Sea are reported. A procedure based on digitonin precipitation has been used to separate the more abundant free sterols from those occurring in esterified forms. Saponification of the solvent extracted sediment residue liberated only a small quantity of residual bound sterols in contrast to studies of other sediments. 4-Methylsterols are much more abundant than 4-desmethylsterols in both the free and esterified sterol fractions which we attribute to a major dinoflagellate input, as in deeper Unit II sediment. The desmethylsterol fraction appears to derive from a variety of sources including dinoflagellates, coccolithophores, diatoms, terrigenous detritus and perhaps invertebrates. 5α(H)-Stanols are particularly abundant in the free sterol fraction. An analysis of the stanol/stenol ratios suggests that the 4-desmethyl-5α(H)-stanols are the result of specific microbial reductions of Δ5-sterols and/or the reflection of a contribution of stanol containing source organisms.  相似文献   

12.
C26, C27, C28 and C29 sterols, including Δ5-, Δ22- and Δ5,22-sterols and both 5α- and 5β-stanols, have been identified in the contemporary lacustrine sediment of Rostherne mere (Cheshire, England). Amounts of total sterols decrease from ca. 400 ppm extracted sediment dry weight for the 0–7 cm sediment section to ca. 40 ppm for the corresponding 18–30 cm section. 5α-stanols are of far greater abundance than the 5α-stanol isomers. The carbon number distributions of unsaturated and saturated sterols and the increase in stanol: Δ5-sterol ratio with sediment depth provide indirect evidence for the operation of a sterol hydrogenation process. C29 sterols preponderate at lower sediment depths, suggesting a predominantly higher plant input, whereas C27 sterols are more abundant in the surface sediment.  相似文献   

13.
Laminated sediments in Baffin Bay, Texas, consist of alternate layers of blue-green algal remains and terrigenous muds. These sediments resemble stromatolites and contain stenols and stannols. The relatively rare C-27, C-28 and C-29 Δ22-5α-stenols and the commonly found Δ5 and Δ5.22 sterols and stannols are present in the Baffin Bay sediments.  相似文献   

14.
Recent sediments from Tanner Basin (off southern California) and Bandaras Bay (in Gulf of California) have been analyzed for normal, isoprenoid and steroidal alcohols using chromatographic (column, GLC, TLC), and spectroscopic (u.v., i.r., MS) methods, prior to and after heat-treatment (from 65 to 150°C). Normal saturated alcohols (C14-C24) and monounsaturated alcohols (C22-C24) were identified, as well as the isoprenoid alcohols, phytol and dihydrophytol.Two series of sterols (Δ5 and Δ7) were found in Tanner Basin, and Δ5-sterols and triterpenes, in Bandaras Bay sediment. Sterols from both sediments contained the corresponding stanols.  相似文献   

15.
Fatty acids have been isolated and quantitatively determined from a 1.5 m sediment core of Lake Suwa, a eutrophic lake in the central districts of Japan.The fatty acids identified by combined gas chromatography-mass spectrometry were straight-chain saturated (C12 to C34), monounsaturated with even carbon number (C16 to C24) and branched-chain (iso, anteiso, 10-methyloctadecanoic) acids. The concentrations of the higher molecular weight (? C20) saturated fatty acids remained nearly constant throughout the core, suggesting a high degree of preservation of those acids, whereas the monounsaturated and the lower molecular weight saturated fatty acids indicated a great decrease in concentration with depth to an approximately 20cm level. It is suggested that the microbial activity in sediments causes a significant reconstruction of the fatty acid distribution during early diagenesis.  相似文献   

16.
The South China Sea(SCS) is one of the most productive and accumulative marginal shelves of organic carbon in the world. To expound the transformation and preservation of organic carbon in the Northeast SCS, where abundant oil and gas resources have been reported, compound specific sterols in free(FR), base hydrolytic(BH), and acid hydrolytic(AH) forms were analyzed in surface and columnar sediments in May, 2016. The results showed that the total contents of sterols detected ranged from 0.15 to 3.74 ppm dry weight in the surface sediments, and gradually decreased from 3.41 to0.17 ppm dry weight from surface to deep sediments, in which cholesterol(27~(△5)) was the most abundant component. Sterols mainly existed in the BH form(54.51%-74.20%), followed by the FR form(25.50%-45.49%) and then the AH form(0-3.77%) in turn, in the surface sediments. BH and FR sterols accounted for 0-49.08% and 50.92%-100% in the columnar sediments, while AH sterols were undetectable. The contents of specific sterols indicated that, the primary source of marine organic carbon was about 5 times as much as that from terrestrial input. More and more FR sterols transformed into BH sterols with increasing sedimentary depth, and BH sterols absolutely dominated in sediment depths under 25 cm. The forms of Sterols C27 were maintained at a relative consistence state, but Sterols C28 to C30 degraded gradually during the sedimentation process. It was suggested that the stability of sterols, based on the chemical structures, might be the primary factor controlling their degradation and preservation in deeper sediments. These results would help to understand the organic carbon(OC) transformation in a hydrate formation area in a marginal sea.  相似文献   

17.
The compositions of sterol, alcohol and ketone fractions from an oxic intertidal surface sediment from Corner Inlet. Victoria, Australia, have been examined by capillary gas chromatographymass spectrometry and related to the lipids of diatoms cultured from the sediment and to lipids of the sea-grass Zostera muelleri. Of the more than thirty sterols in the sediment most appear to derive from diatoms, including the major sterol 24-methylcholesta-5.22E-dien-3β-ol. Small amounts of 24-ethylcholesterol probably derive from Zostera, with a minor diatom contribution. 5α-stanols, both fully saturated and with a side-chain double bond, represented ca. 14% of the total sterols: a significant proportion of these are probably derived from marine invertebrates. These organisms also contribute C26 sterols. most of the cholesterol and possibly small amounts of Δ-sterols. The data suggest that in situ biohydrogenation of stenols was not a major process in sterol transformation in the surface oxic sediment. Alcohols ranged from C12 to C30 and showed an unusual abundance of unsaturated components with Δ9-16:1 being the major constituent. The long-chain alcohols probably originate largely from Zostera but the shorter-chain. C12-C20. alcohols are at least partly derived from wax esters of unknown origin. Diatoms do not contribute significant amounts of alcohols. Ketones were not major constituents of the sediment and consisted mainly of 6.10.14-trimethylpentadecan-2-one and a series of n-alkan-2-ones ranging from C16 to C33. The latter showed a similar distribution to that of the n-alkanes but the correspondence was not sufficient to substantiate a product-precursor relationship. Very long-chain C3- C39 unsaturated methyl and ethyl ketones, which may originate from the marine unicellular alga Emiliania huxleyi. were present in low concentration.  相似文献   

18.
In freshwater settings, dinosterol (4α,23,24-trimethyl-5α-cholest-22E-en-3β-ol) is produced primarily by dinoflagellates, which encompass various species including autotrophs, mixotrophs and heterotrophs. Due to its source specificity and occurrence in lake and marine sediments, its presence and hydrogen isotopic composition (δD) should be valuable proxies for paleohydrological reconstruction. However, because the purity required for hydrogen isotope measurements is difficult to achieve using standard wet chemical purification methods, their potential as a paleohydrological proxy is rarely exploited. In this study, we tested δD values of dinosterol in both particulate organic matter (POM) and sediments of stratified tropical freshwater lakes (from Cameroon) as a paleohydrological proxy, the lakes being characterized by variable degrees of eutrophication. In POM and sediment samples, the δD values of dinosterol correlated with lake water δD values, confirming a first order influence of source water δD values. However, we observed that sedimentary dinosterol was D enriched from ca. 19 to 54‰ compared with POM dinosterol. The enrichment correlated with lake water column conditions, mainly the redox potential at the oxic–anoxic interface (Eh OAI). The observations suggest that paleohydrologic reconstruction from δD values of dinosterol in the sediments of stratified tropical lakes ought to be sensitive to the depositional environment, in addition to lake water δD values, with more positive dinosterol δD values potentially reflecting increasing lake eutrophication. Furthermore, in lake sediments, the concentration of partially reduced vs. non-reduced C34 botryococcenes, stanols vs. stenols, and bacterial (diploptene, diplopterol and ββ-bishomohopanol) vs. planktonic/terrestrial lipids (cholesterol, campesterol and dinosterol) correlated with Eh OAI. We suggest using such molecular proxies for lake redox conditions in combination with dinosterol δD values to evaluate the effect of lake trophic status on sedimentary dinosterol δD values, as a basis for accurately reconstructing tropical lake water δD values.  相似文献   

19.
The abundance of sterols in sediment depth profiles is determined by variations in input source abundances and diagenesis. Deconvolution of these variables would permit accurate estimation of degradation rates and initial input source contributions of sterols to the sediments. In this study we have demonstrated the application of a simple mathematical approach to the estimation of the relative stabilities of a range of sterols in a microbially-poor temperate intertidal sediment. The results indicate that st-5-enols and possibly 4-methyl sterols are less stable than other sterols in this environment. Since dehydration reactions of sterols would be favoured by both a 4-methyl substituent and a C5,6 double bond, whilst other processes would not be as selective, it seems probable that this abiological process predominates in the Corner Inlet sediments.  相似文献   

20.
The top five centimeters of sediment collected at the deepest point of Lake Léman (Switzerland), 309 meters below water level, contain concentrations of 5α(H)-cholestan-3α-ol (epicholestanol) up to 10% of the total sterol content. Isobutane chemical ionization mass spectrometry and coinjection with an authentic standard on a SP-1000 glass capillary column were used in order to successfully characterize this epimer of cholestanol.The distribution of this stanol throughout the sediment core studied suggests in situ bacterial production. The change in concentration of epicholestanol with depth is different from those found for other C27 stanols, such as cholestanol or coprostanol. It is probably the result of a change in the bacterial fauna in the most recently deposited sediment, related to the increasing eutrophication of the lake rather than the consequence of its lower stability due to the axial conformation of the OH substituent.  相似文献   

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