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1.
The concentration of solvent-extractable (SE) and bound hydrocarbons, ketones, alcohols, sterols, monocarboxylic acids, hydroxyacids and α,ω-dicarboxylic acids of a surface sample (0–2.5 cm) from a recent carbonate tropical sediment taken at 60ft (18m) depth north-west of the Low Isles, North Queensland, are reported in detail. n-Alkanes are a minor constituent in the SE and bound hydrocarbon fractions with the major component being unresolved complex hydrocarbon material which is not an anthropogenic input. 6,10,14-Trimethylpentadecan-2-one derived from chlorophyll, as well as phytol, were identified as major components of the ketone and alcohol constituents. No chlorophyll pigments or pigmented degradation products were present, implying degradation before incorporation into the sediment. This conclusion is consistent with evidence for higher-plant input in which all sensitive lipids have been degraded before incorporation. SE and bound fractions have been studied in detail and show considerable differences probably arising from the importance of viable biomass in the SE fraction. Inputs to the sediment are determined as higher plants, algae, bacteria, fungi and meiofauna in descending order of importance.  相似文献   

2.
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3.
In order to study the first steps of incorporation of lipids in recent organic-rich sediments into free and bound fractions, we have selected the Santa Barbara Basin, off California. This basin with a maximum of 590 m water depth is characterized by high phytoplankton production in surface waters and a low oxygen content in bottom waters. Sediments show the following features: high sedimentation rate ≈ 4 mm/yr, no bioturbation, and development of a bacterial mat community at the surface with predominance of sulphur-oxidizing bacteria trapping particles, thus preventing re-distribution of sediment, which permit a unique observations of organic sedimentation on a new few years basis.A sediment core has been divided into 2 cm thick slices corresponding to a time resolution of ≈5 years, from 1835 up to 1987. Samples have been analyzed using a multi-parameter approach, such as for plankton species identification, carbon stable isotope ratios and, as reported here, for lipid organic tracers. Organic tracers have been analyzed in the sterol and fatty series for both free and bound compounds by gas chromatography and gas chromatography/mass spectrometry.The incorporation processes of sterols with depth appear different for free and bound compounds. Total free sterol concentrations show high values in surface sediments (≈ 100 μg/g dry sediment), rapidly decrease up to ≈ 10 cm depth and remain at a constant value of 30–40 μg/g. Total bound sterol concentrations show low values in surface sediment (13.6 μg/g), and vary irregularly with depth up to a value of 55 μg/g at 7.3 m, and then remain constant at 25–26 μg/g.Profiles of evolution with depth of free C27, C28 sterols show a regular decrease, whereas C29 sterols show an irregular decrease with anomalies at 7.3 cm (approximately age: 1977–1978) and at 14.1 cm (1962–1964). Profiles of bound compounds are rather different, very regular for C28 sterols, irregular with oscillations for C27 and C29 sterols at 7.3, 12.2 and 18.0 cm (1954–1956), suggesting a different mode of incorporation and probably different inputs for C27, C29 and C28 sterols.The study of the kinetics of degradation of sterols between surface (1987) and 10.5 cm (1968–1972) shows that C27 compounds are degraded at a slight higher rate (0.53 μg/μg of initial C27 concentration/ year) than are C28 and C29 compounds (0.047 μg/μg of initial concentration/year). An intermediate value is found for brassicasterol: 0.049 μg/μg/year.  相似文献   

4.
Esters of phytol or related isoprenoid acids and fatty acid esters of pentacyclic triterpenoid alcohols and sterols have been isolated from lacustrine sediments varying in age from contemporary to c. 50,000 years old. The esters were analysed by C-GC-MS and identified by GC retention data and mass spectral interpretation based on comparison with authentic compounds.In surface sediment of a productive lake, phytyl and steryl esters are biochemical markers of input from algal and Zooplankton sources. Esters of pentacyclic triterpenols detected in an older, peat-derived sediment may reflect constituents of peat-forming plant species. In sediments derived mainly from terrestrial organic matter, steryl esters containing the same acyl group showed a lower stanol/Δ5-stenol ratio than did the corresponding free sterols.  相似文献   

5.
Recent sediments from an oligotrophic lake (Loch Clair) having uniform organic input for 2000 yr show changes in lipid abundance and composition, with increasing depth, attributed to diagenesis. Stability of free lipids decreases in the order n-alkanes, alkan-2-ones, sterols, n-alkanoic acids, n-alkanols, n-alkenoic acids. Diagenetic loss of shorter-chain homologues is complete within 400 yr. Stabilisation of bound relative to free lipids increases the proportion of the former with sediment age and reduces loss of shorter-chain bound homologues.In an eutrophic lake (Cross Mere), shorter-chain free and bound sedimentary lipids show increased abundance compared with Loch Clair. The relative importance of higher input of shorter-chain lipids derived from aquatic detritus, and slower initial diagenesis due to the anoxic hypolimnion, as causative factors for this difference between lake types cannot yet be assessed.  相似文献   

6.
Fatty acids and isoprenoid alcohols were analyzed in river, estuarine, and coastal sediment cores: (1) to investigate the distribution of these lipids among the unbound phase. those bound or closely associated with humic substances, and those bound or closely associated with the huminkerogen and clay mineral matrix. (2) to investigate the diagenetic changes of these lipids with depth in the sediments. and (3) to obtain information on the use of these compounds as organic tracers in marine sediments.Results confirm earlier observations that fatty acids are rapidly altered in marine sediments Both the total and the individual fatty acids decrease in concentration with depth in the sediments: unsaturated acids decrease faster than saturated acids and unbound acids decrease faster than bound acids Approximately 8–62% of the fatty acids were unbound. 2–22% were associated with humic substances. and 38–86% were associated with the residual organic-mineral matrix. Qualitative differences also exist between the fatty acids associated with the unbound, humic, and residual fractions. The ratio of trans/cis geometric isomers of the fatty acids generally increases downcore. with no rearrangement of the double bond positions within the molecules. Either the cis isomer is being preferentially degraded with depth in the sediments, or there is a low temperature, clay catalyzed conversion of the cis isomers to the trans isomers occurring down the cores.Phytol was the major alcohol present in the sediments and does not appear to be altered as rapidly as the fatty acids. Less than 10% of the total phytol (PHY) plus dihydrophytol (DHP) was present as DHP and no trend could be discerned between PHY and DHP with depth or with unbound, humic, and residual material in the cores. All of the isolated DHP appeared to be present as the RRR stereoisomer. Along with the absence of phytane in the cores, this observation suggests that the reduction of phytol to dihydrophytol is microbially mediated in the upper layer of the sediment.  相似文献   

7.
We analyzed trends in a 23-year period of water quality and biotic data for Chesapeake Bay. Indicators were used to detect trends of improving and worsening environmental health in 15 regions and 70 segments of the bay and to assess the estuarine ecosystem’s responses to reduced nutrient loading from point (i.e., sewage treatment facilities) and non-point (e.g., agricultural and urban land use) sources. Despite extensive restoration efforts, ecological health-related water quality (chlorophyll-a, dissolved oxygen, Secchi depth) and biotic (phytoplankton and benthic indices) metrics evaluated herein have generally shown little improvement (submerged aquatic vegetation was an exception), and water clarity and chlorophyll-a have considerably worsened since 1986. Nutrient and sediment inputs from higher-than-average annual flows after 1992 combined with those from highly developed Coastal Plain areas and compromised ecosystem resiliency are important factors responsible for worsening chlorophyll-a and Secchi depth trends in mesohaline and polyhaline zones from 1986 to 2008.  相似文献   

8.
Organic materials in lacustrine sediments are from multiple terrestrial and aquatic sources. In this study, carbon (δ13C) and hydrogen isotopic compositions (δD) of phytol, various sterols, and major n-fatty acids in sediments at Lake Haruna, Japan, were determined in their solvent-extractable (free) and saponification-released forms (bound). The δ13C-δD distributions of these lipid molecules in sediments are compared with those of terrestrial C3 and C4 plants, aquatic C3 plants, and plankton to evaluate their relative contributions. δ13C-δD of free phytol in sediments is very close to that of phytol in plankton samples, whereas δ13C-δD of bound phytol in sediments is on a mixing line between terrestrial C3 plant and plankton material. Unlike phytol, no significant δ13C-δD difference between free and bound forms was found in sterols and n-fatty acids. δ13C-δD values of algal sterols such as 24-methylcholesta-5,22-dien-3β-ol in sediments are close to those of plankton, whereas δ13C-δD of multiple-source sterols such as 24-ethylcholest-5-en-3β-ol and of major n-fatty acids such as n-hexadecanoic acid in sediments are between those of terrestrial C3 plants and plankton samples. Thus, δ13C-δD distributions clearly indicate the specific source contributions of biomarkers preserved in a lacustrine environment. Free phytol and algal sterols can be attributed to phytoplankton, and bound phytol, multiple source sterols, and major n-fatty acids are contributed by both terrestrial C3 plants and phytoplankton.  相似文献   

9.
Muddy carbonate deposits near the Dry Tortugas, Florida, are characterized by high organic carbon remineralization rates. However, approximately half of the total sedimentary organic matter potentially supporting remineralization is occluded in CaCO3 minerals (intracrystalline). While a portion of nonintracrystalline organic matter appears to cycle rapidly, intracrystalline organic matter has an approximately constant concentration with depth, suggesting that as long as its protective mineral matrix is intact, it is not readily remineralized. Organic matter in excess of intracrystalline organic matter that is preserved may have a variety of mineral associations (e.g., intercrystalline, adsorbed or detrital). In surface sediment, aspartic acid contributed ∼22 mole % and ∼50 mole % to nonintracrystalline and intracrystalline pools, respectively. In deeper sediment (1.6-1.7m), the composition of hydrolyzable amino acids in both pools was similar (aspartic acid ∼40 mole %). Like amino acids, intracrystalline and nonintracrystalline fatty acids have different compositions in surface sediments, but are indistinguishable at depth. These data suggest that preserved organic matter in the nonintracrystalline pool is stabilized by its interactions with CaCO3. Neutral lipids are present in very low abundances in the intracrystalline pool and are extensively degraded in both the intracrystalline and nonintracrystalline pools, suggesting that mineral interactions do not protect these compounds from degradation. The presence of chlorophyll-a, but absence of phytol, in the intracrystalline lipid pool demonstrates that chloropigments are present only in the nonintracrystalline pool. Sedimentary chloropigments decrease with depth at similar rates in Dry Tortugas sediments as found in alumino-silicate sediments from the Long Island Sound, suggesting that chloropigment degradation is largely unaffected by mineral interactions. Overall, however, inclusion and protection of organic matter by biominerals is a major pathway for organic matter preservation in this low-organic carbon, biomineral-rich regime.  相似文献   

10.
若尔盖高原全新世气候序列的类脂分子化石记录*   总被引：3，自引：0，他引：3  
基于可靠的年代标尺,结合青藏高原泥炭沉积剖面的有机碳、孢粉等相关资料,首次在该区利用类脂分子化石指标建立了全新世以来的气候与环境演化序列。结果表明,正构烷烃、脂肪酸和脂肪醇等类脂分子化石指标存有意义的规律性变化。其中,反映低等菌藻生物和高等植物相对变化的轻组分与重组分之比L/H以及平均碳链长度ACL具有很好的古气候意义,即L/H高,ACL低,指示气候偏暖湿;L/H低,ACL高,指示气候偏干冷。各个类脂分子化石指标记录的气候信息在细节上具有一定的差异,可能是不同类脂物分子的地球化学行为和生物组成结构的不同以及对气候因素温湿组合变化响应各异的体现。同时,也较好地揭示了类脂分子化石具有自己的敏感性,在细节上较传统的有机碳指标在记录气候信息上更为敏感。该研究进一步突出了这些泥炭类脂分子化石在第四纪研究中的重要地位和应用潜力。  相似文献   

11.
The relationship between the lipid composition of organisms in the water column of an eutrophic lake and the lipid composition of underlying sediments, previously examined for n-alkanols and steroids, is now reported for hydrocarbons, ketones and carboxylic acids.The n-C7 alkane and alkenoic acids from two primary sources are rapidly metabolized in the water column and surficial sediment. Bacterial biomarkers, including hopenes and fatty acids, were detected in the photosynthetic bacterial layer occurring just above the sediment-water interface.Within the sediment the apparent conversion of free n-alkanes, alkan-2-ones and ω-hydroxy acids to the corresponding bound form is noted; microbiological oxidation of n-alkanes to alkan-2-ones is supported by the detection of the intermediate alkan-2-ols with a distribution similar to that of the ketones. The geochemistry of sediment deposited c. 1900, prior to biological study of the site, was interpreted from stable biomarkers and the diagenetic changes recognised in the study of contemporary deposition. A qualitative difference in algal input to the older sediment is inferred from the low Δ7-sterol content and presence of 2,6,10-trimethyl-7-(3-methylbutyl)-dodecane. However, there was still significant dinoflagellate input, as indicated by the presence of 4α-methylsterols. A difference in higher-plant input to the older sediment, indicated from the n-alkane, alkene and triterpenoid ketone distributions, is consistent with the recent development of tree cover.  相似文献   

12.
Several isoprenoid compounds were isolated from a heat-treated marine sediment in the southern California continental shelf (from Tanner Basin) which were not present in the original sediment. Among the compounds identified were: phytol, dihydrophytol, C18-isoprenoid ketone, phytanic and pristanic acids, C19- and C20-monoolefins, and the alkanes 2,6,10-trimethylpentadecane, pristane and phytane. The significance and possible routes leading to these compounds is discussed.  相似文献   

13.
We compared the degradation behaviour of amino sugars (ASs) and amino acids (AAs) during sedimentation in two lakes. Concentrations of individual ASs and AAs were measured in plankton, sediment trap and sediment samples from Lake Zug (LZ; eutrophic, stratified, permanently anoxic below 170 m) and Lake Brienz (LB; oligotrophic, oxic throughout the water column). In the plankton samples AAs comprised 37–50% of the organic carbon (Corg) and 41–65% of the N. With increasing water depth the fraction of Corg and N as AAs almost halved in both lakes. At the sediment surface the contribution of AAs to the Corg pool was slightly greater, but in the sediments the proportion further decreased downwards to values of 1% of the Corg pool in LB and 8% in LZ, and 3% and 17% of the N pool, respectively. ASs contributed to a smaller extent to the planktonic organic matter (OM). Within the water column, the contribution decreased in both lakes. In contrast, in the sediments the contribution of ASs to the Corg and N pools increased slightly with depth, indicating AS accumulation. We applied degradation indices based on ASs, AAs and chlorins, which all revealed transformation with OM sedimentation. However, some indices were more sensitive to early degradation (e.g. reactivity index) and others to an intermediate level of degradation (e.g. chlorin index and non-protein AAs). Despite the different trophic status and redox conditions, the general pattern of degradation was similar in both lakes, but was more pronounced in the sediments of the eutrophic LZ.  相似文献   

14.
The endorheic Lake Van in eastern Anatolia (Turkey) is the world’s largest soda lake and it is an important site in paleoclimate studies to understand past continental conditions in western Asia. In order to gain further insights into the biomarker signatures in Lake Van’s sediments we have analyzed particulate material in sediment traps deployed between August 2006 and July 2007. The biomarkers used were long chain alkenones (LCAs C37-C39, haptophyte lipids), isoprenoid glycerol dialkyl glycerol tetraethers (GDGTs, Archaea membrane lipids) and pigments (chlorins and fucoxanthin). The biomarker fluxes indicate a strong seasonality in export primary productivity and the phytoplankton community structure. The highest total mass and organic carbon fluxes were found in summer, coupled to strong stratification while the lowest mass fluxes occurred in winter at the time of water column mixing. With increasing temperatures in early spring, phytoplankton export productivity grew, coupled with an increase of total mass flux and organic carbon, which might be associated to enhanced nutrient input from snowmelt runoff. The percentage of C37:4 shows some correspondence with observed seasonal changes in Lake Van’s stratification structure. We also evaluated the potential applicability of molecular temperature proxies derived from Archaea and haptophyte lipids. The use of the TEX86 proxy was precluded by low GDGT abundances. Estimated LCA temperatures were consistent with temperatures in the photic zone but no seasonality changes were observed despite the wide annual temperature range measured at Lake Van.  相似文献   

15.
Hopanoids bound into the insoluble organic matter (kerogen) of Recent sediments from a freshwater lake (Priest Pot) and an anoxic sulphidic fjord (Framvaren) were released by hydropyrolysis and examined by gas chromatography-mass spectrometry. Bound hopanoids are present in high concentration (190-1400 μg/g TOC) and represent 22 to 86% of the total analysable hopanoids (i.e., bound and solvent-soluble), this proportion increasing with depth in Framvaren Fjord. The hopanes generated by hydropyrolysis contain higher amounts of the C35, C32, and C30 homologues, reflecting the carbon number distribution of the bound hopanoids and indicating that both biohopanoids (C30 and C35) and their diagenetic products (dominated by C32) are incorporated into the kerogen on a timescale of only 0 to 350 years. Sequential (multiple temperature) hydropyrolysis experiments gave an indication of the relative strengths of bonds being cleaved in association with hopane generation: The hopanoids of a sediment from Priest Pot are almost entirely bound by strong covalent bonds, interpreted to be mainly ether linkages, whilst a Framvaren sediment contains hopanoids that are bound by a mixture of weak di-/polysulphide linkages and stronger ether bonds. Labelling with deuterium indicated that the strong covalent linkages dominate, even for the Framvaren sediment.  相似文献   

16.
Homologous series of 2- and 3-hydroxy fatty acids occur in both the free and the bound lipid fractions of an oligotrophic lacustrine sediment (Loch Clair, N.W. Scotland). The stereochemistry of each constituent was assigned by gas chromatographic separation of diastereoisomeric O-2(S)-phenylpropionyl methyl ester derivatives. Free and bound 2-hydroxyacids above C20 showed the R configuration characteristic of by-products formed during fatty acid metabolism by α-oxidation. In the C14–C18 region, bound 2- and 3-hydroxyacids show the R configuration more dominantly than the corresponding free lipids. These bound 2(R)- and 3(R)-hydroxyacids are attributed to microbial cell wall lipids.  相似文献   

17.
用GC-MS对湖北清江岩溶地区和尚洞洞顶植物叶片与该洞上覆土壤层中的类脂物进行了分析和对比。在植物叶片中检测出了一系列直链烷烃、脂肪酸、以及丙三醇、植醇和甾醇等类脂物,其中直链烷烃的碳数分布范围大体在C21～C36之间,以C29或C31为主峰且具有奇偶优势;脂肪酸的分布主要集中在中、短链脂肪酸内（C数<23）,以C16为主峰呈单峰型分布且具有偶奇优势;醇的分布很不规则,仅检测出丙三醇,植醇和三种甾醇,没有检测到脂肪酮类化合物。与之相比,洞顶上覆土壤层中检测出更加丰富的类脂物。类脂物具有如下特征:正构烷烃以C31为主峰,还存在低碳数正构烷烃和异构烷烃,如2-甲基、3-甲基、4-甲基、5-甲基、6-甲基、7-甲基、8-甲基等一系列的单甲基支链烷烃,这些支链烷烃显示了微生物的贡献;脂肪酸分布也以低碳数的C16为主峰,且低碳数脂肪酸的含量较植物叶片中明显的增加,同时一些异构和反异构脂肪酸（C14∶0,C15∶0和C17∶0）以及一些单不饱和脂肪酸（C16∶1,C17∶1,C18∶1和C20∶1）也被检测到,也表明土壤中的脂肪酸不仅存在高等植物的贡献,还存在微生物的来源;没有植醇,但出现姥鲛烷和植烷并检测到了一系列脂肪醇化合物,碳数分布在C21～C36之间;检测到一系列的酮,具有奇偶优势,碳数分布范围在C23～C30和C33。高等植物叶片和土壤的差异反映了微生物对高等植物类脂物输入到土壤过程的重要贡献。本研究工作不仅提供了该岩溶地区植物叶片的类脂物信息,还为研究土壤有机质的来源和植物叶片中类脂物在地质过程中的转变提供信息,更为研究岩溶地区滴水和石笋中类脂物的来源提供一定的参考。  相似文献   

18.
Sediment and heavy metal accumulation in the Cauvery basin   总被引：2，自引：0，他引：2  
Eleven cores were collected from the Cauvery basin. Radiometric dates were used to determine modern sediment accumulation rates. Sediment accumulation rates ranged from 0.4 to 4 mm yr–. Heavy metal concentration decreases with the increase of depth. The heavy metal concentrations at certain depths are attributed to the irregular input of metals and their remobilization. Heavy metal accumulations have been computed using sediment accumulation rates, and accumulation rates show an additional anthropogenic input of metals and sediments in the recent past. Factor analysis and correlation analysis show the diverse source and accumulation mechanism influencing the metal distribution in the basin.  相似文献   

19.
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   

20.
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   

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