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1.
Long-chain fatty acids (C10-C32), as well as C14-C21 isoprenoid acids (except for C18), have been identified in anhydrous and hydrous pyrolyses products of Green River kerogen (200–400°C, 2–1000 hr). These kerogen-released fatty acids are characterized by a strong even/odd predominance (CPI: 4.8-10.2) with a maximum at C16 followed by lesser amounts of C18 and C22 acids. This distribution is different from that of unbound and bound geolipids extracted from Green River shale. The unbound fatty acids show a weak even/odd predominance (CPI: 1.64) with a maximum at C14, and bound fatty acids display an even/odd predominance (CPI: 2.8) with maxima at C18 and C30. These results suggest that fatty acids were incorporated into kerogen during sedimentation and early diagenesis and were protected from microbial and chemical changes over geological periods of time. Total quantities of fatty acids produced during heating of the kerogen ranged from 0.71 to 3.2 mg/g kerogen. Highest concentrations were obtained when kerogen was heated with water for 100 hr at 300°C. Generally, their amounts did not decrease under hydrous conditions with increase in temperature or heating time, suggesting that significant decarboxylation did not occur under the pyrolysis conditions used, although hydrocarbons were extensively generated.  相似文献   

2.
The black shale samples collected from two Neogene formations in the Klias Peninsula area, West Sabah, have been assessed and characterized in details by gas chromatography, gas chromatography-mass spectrometry and a variety of organic geochemical parameters. The aims of this study are to describe the characteristics of organic matter of these sediments in terms of source/type of the organic matter, assess its thermal maturity and paleoenvironment of deposition, based primarily on biomarker distributions. The results of both formations do not reveal significant differences within the rock extracts. The gas chromatograms of the saturated hydrocarbon fractions of the Setap Shale and the Belait formations displayed monomodal n-alkane distributions and nearly identical regular sterane compositions with a predominance of C27 regular steranes. These are consistent with open marine depositional environments dominated by marine biological matter. Another related feature of these rock extracts is the presence of a high relative abundance of gammacerane, indicating anoxic marine hypersaline source depositional environment. The relatively high abundance of common land plant-derived biomarkers, such as bicadinanes and oleananes, is a clear indication of a major terrigenous input to the source of the extractable organic matter. The predominance of oleanane biomarkers in both formations is indicative of angiospermis input and Tertiary source rocks. The high C29/C30 hopane ratios, moderate development of C33–C35 hopanes, high abundance of tricyclic terpanes and a slight predominance of C27 regular sterane over C28 and C29 steranes are characteristic features tending to suggest a significant marine influence on these source rocks, thereby suggesting a mixed source input. The 22S/(22S+22R)C32 hopane ratio has reached equilibrium, and this is supported by the high maturity level as indicated by the 22S/22SC31–33 extended hopane ratios and 20S/(20S+20R)C29 regular steranes ratios.  相似文献   

3.
Based on the compositions and distributions of biomarkers in thirty-five representative oil samples, oils from the Tarim Basin of northwestern China are mainly divided into two oil families. One oil family contains relatively low amounts of C15-C20 isoprenoid hydrocarbons and shows pristane predominance with Pr/Ph ratios ranging from 1.50 to 3.00. The GC/MS analytical data of these oils show the occurrence of abundant hopanes, and low concentrations of steranes and tricyclic terpanes with hopanes/steranes ratios from 6.25 to 12.24 and tricyclic terpanes/hopanes ratios from 0.03 to 0.24. These oils contain low drimane relative to homodrimane (C15/C16 < 1.0) and abundant rearranged bicyclanes in bicyclic sesquiterpanes. They are dominated by low carbon number (C19-C21) compounds in the tricyclic terpanes, and are rich in rearranged hopanes, C29Ts and an unknown C30 compound in pentacyclic triterpanes. These geochemical characteristics suggest that the oils were generated mainly from terrigenous organic matter. The other oil family shows remarkably different biomarker compositions and distributions. The oils revealed Pr/Ph ratios of about 1.0, high drimane/homodrimane ratios (>1.0), low hopanes/steranes ratios (0.65–2.50), high tricyclic terpanes/hopanes ratios (0.30–2.00) and a dominant peak at C23 in tricyclic tepanes, suggesting a marine organic origin. Oil-source rock correlation indicates that these two oil families seem to have been derived from Mesozoic Jurassic-Triassic terrestrial source rocks (shales and coal seams) and Lower Paleozoic Ordovician-Cambrian marine source rocks, respectively.  相似文献   

4.
本文以油苗抽提物的饱和烃色谱-质谱分析为基础,剖析了羌塘盆地昂达尔错地区油苗的生物标志化合物特征,探讨了其沉积环境和成熟度指示意义。昂达尔错油苗含有丰富的正构烷烃、类异戊二烯烃、萜类化合物和甾类化合物。正构烷烃轻烃组分含量较高,无明显的奇偶优势。Pr/Ph比小于1,显示一定的植烷优势。萜类化合物中五环三萜烷相对含量最高,四环萜烷含量最少,并有一定的伽马蜡烷和升藿烷分布。规则甾烷相对含量为C27C29C28,呈不对称"V"字形分布,异构化成熟度参数值较高,且4-甲基甾烷化合物普遍存在。昂达尔错油苗母源岩沉积于具有较高盐度的还原环境,以藻类、菌类等海相有机质输入为主,油苗有机质处于成熟阶段。  相似文献   

5.
The distribution of methyl-2-methyl-2-(4,8,12-trimethyltridecyl)chromans (M - MTTC) is related to sedimentary environments. 5,7,8 - tri-Me-MTTC, 5,8 -di - Me-MTTC and 7,8 - di - Me - MTTC have been found in coal for the first time, implying that M-MTTC is widely spread in sediments.The distribution of M - MTTC. the presence of C32—C35 benzohopanes, high Pr/Ph ratio, obvious even - odd predominance in C24—C34 alkanes and odd-even predominance in normal alkanes provide strong evidence of a near - shore lacustrine environment.  相似文献   

6.
《Applied Geochemistry》2004,19(1):55-72
Bulk and molecular stable C isotopic compositions and biomarker distributions provide evidence for a diverse community of algal and bacterial organisms in the sedimentary organic matter of a carbonate section throughout the Permian–Triassic (P/Tr) transition at the Idrijca Valley, Western Slovenia. The input of algae and bacteria in all the Upper Permian and Lower Scythian samples is represented by the predominance of C15–C22 n-alkanes, odd C-number alkylcyclohexanes, C27 steranes and substantial contents of C21–C30 acyclic isoprenoids. The occurrence of odd long-chain n-alkanes (C22–C30) and C29 steranes in all the samples indicate a contribution of continental material. The decrease of Corg and Ccarb contents, increase of Rock-Eval oxygen indices, and 13C-enrichment of the kerogen suggest a decrease in anoxia of the uppermost Permian bottom water. The predominance of odd C-number alkylcycloalkanes, C27 steranes, and C17 n-alkanes with δ13C values ∼−30‰, and 13C-enrichment of the kerogens in the lowermost Scythian samples are evidence of greater algal productivity. This increased productivity was probably sustained by a high nutrient availability and changes of dissolved CO2 speciation associated to the earliest Triassic transgression. A decrease of Corg content in the uppermost Scythian samples, associated to a 13C-depletetion in the carbonates (up to 4‰) and individual n-alkanes (up to 3.4‰) compared to the Upper Permian samples, indicate lowering of the primary productivity (algae, cyanobacteria) and/or higher degradation of the organic matter.  相似文献   

7.
This study elucidates the geothermal influence of a salt dome on the diagenesis of organic matter present in sedimentary sequences directly overlying the salt strata. Despite similarities in geological setting, geochemical characteristics in sedimentary column and proximity of location (～3 km), the exploratory wells Adolphus 2-k-41 and D-50 drilled on the crest and flank of a salt dome respectively, show considerable differences in the quantitative and qualitative distribution of hydrocarbons. The well drilled on the crest of the salt dome tested oil of 31°APl gravity. The concentrations of gaseous (C1-C4) and heavy (C15+) hydrocarbons of this well were several times higher than those found in the corresponding sequences of a flank well. The coloration studies of isolated kerogen and gas chromatographic investigations of hydrocarbons suggest that the organic matter present in Adolphus 2-k-41 has undergone a greater degree of thermal alteration than that of D-50. The heat radiating from the salt strata is believed to be responsible for the early diagenesis of the organic matter.  相似文献   

8.
The distributions of lipids in surface and subsurface sediments from the northern South China Sea were determined. The n-alkanes were in bimodal distribution that is characterized by a centre at n-C16 –n-C20 with maximum at C18(or C19) and n-C27 –n-C31 as well as at C29(or C31). The short-chain alkanes suffered from significant losses due to their slow deposition in the water column, and their presence with a slight even carbon predominance in shallow seafloor sediments was ascribed mainly to the direct input from the benthos. The long-chain alkanes with odd predominance indicate transportion of terrigenous organic matter. Immature hopanoid biomarkers reflect the intense microbial activity for bacteria–derived organic matter and the gradual increase of maturity with burial depth. Abundant n-fatty acid methyl esters(n-FAMEs) that are in distributions coincident with fatty acids were detected in all samples. We proposed that the observed FAMEs originated from the methyl esterification of fatty acids; methanol production by methanotrophs and methanogenic archaea related to the anaerobic oxidation of methane, and sulfate reduction provided an O–methyl donor for methylation of fatty acids. The CH4 released from hydrate dissociation at oxygen isotope stage II of Cores ZD3 and ZS5, which had been confirmed by the occurrence of negative δ13C excursion and spherical pyrite aggregates, could have accelerated the above process and thus maximized the relative content of FAMEs at ZD3-2(400–420 cm depth) and ZS5-2(241–291 cm depth).  相似文献   

9.
In order to improve understanding of the stratigraphy of the Lake Turkana Basin, one of the important sites in the evolution of early man, this study evaluates the usefulness of organic biological marker compounds, n-alkanes and fatty acids, for correlation of isolated sedimentary strata.Eighty-five paleosol samples were collected from well-defined sedimentary horizons in two regions (Area 103 and Area 130) of the Koobi Fora area of Lake Turkana. Results indicate that most of the organic matter present was derived from terrestrial plant waxes. In sediments where extensive diagenesis has occurred, microbial input of organic matter may have been substantial. Algae were either not an important source of organic matter, or their marker compounds have been removed or altered by degradative processes.The fate of the original paleosol organic matter has been governed to some extent by weathering processes, especially in Area 130. Weathering decreased the amount of extractable lipids, particularly fatty acids and the low molecular weight alkanes (C17C20); produced or retained relatively large amounts of alkanes greater than C21 within a unimodal distribution; and lowered CPI values. Consequently, stratigraphic correlation by unique alkane and fatty acid distributions has been confined to short distances (many meters).Both n-alkanes and fatty acids have been retained better by association with clay minerals than by sand matrices. The alkane distribution of sandstones differs from that of clay organics in having a narrower carbon chain length distribution and lower CPI values. In Area 103, where weathering was less severe, compositional variations with stratigraphic position indicate that lipid material has been retained within each of the facies examined.  相似文献   

10.
n-Alkanes in the soluble organic matter extracted from a series of vitrinite and sporinite concentrates have been analysed by gas chromatography. The macerals were isolated from coals ranging in rank from 77.1% to 86.6% carbon (vitrinite: dry, ash-free), and yields of n-alkanes ranged from 10 to 580 ppm for vitrinites and from 20 to 970 ppm for sporinites. The maximum yields were found at a rank of 85.4% C from vitrinites and 86.6% C from sporinites.Distribution maxima of the n-alkanes, as shown by gas chromatography, range from C27 and C29 at lower ranks to as low as C16 at higher ranks. The distributions also show a progressive decrease in the preference of odd-carbon-number homologues with increasing rank. Virtually smooth distributions were attained in high-volatile bituminous A coals. Quantitative data show that the loss of the odd-carbon-number preference occurred, for the most part, while individual long-chain homologues increased in concentration.There is a progressive increase in the amounts of shorter-chain n-alkanes with increasing rank. It is suggested that sequential processes may have occurred whereby the rate of formation of long-chain n-alkanes in high-volatile bituminous A rank macerals becomes slower than their rate of subsequent fragmentation to shorter chain lengths. Consequently, assuming derivation from the insoluble maceral matrices, the chain-length distributions of parent n-alkyl structures within the insoluble material may retain characteristics pertaining more to the nature of the source organic matter at the time of deposition than do the extractable n-alkane patterns, especially at higher ranks.  相似文献   

11.
Peats in a sediment core from Ruoergai bog, which has a cold and moist plateau climate with major source input from herbaceous plants, have been studied by GC–MS in order to understand the composition and diagenetic processes of lipids in this depositional environment. Long chain components (C21–C35) predominate in the n-alkanes, n-alk-1-enes, n-fatty acids, n-alkan-2-ones and n-alkanols with a maximum of C31, C27, C22 or C24, C23 or C25 and C22, respectively. A herbaceous origin for these long chain compounds is suggested, and this is supported by their stable carbon isotopic compositions. Diterpenoid hydrocarbons with abietane, pimarane and kaurane skeletons, some of which have not been reported often in modern sediments, are prominent and are derived from higher plants. Several triterpenoid ketones and alcohols with oleanane or lupane skeletons, and a series of des-A-triterpenoid hydrocarbons which have not been reported often in modern sediments are also present, and are assigned to a higher plant source. Hopanoids, including their alkanes, alkenes, ketones, alcohols and esters, are abundant and of bacterial origin. Steroid ketones and alkanols are dominated by C29 homologues. C28 and C29 steroids are derived mainly from higher plants, whereas the C27 component is assigned to a microbial source. The presence of short-chain n-alkanes with no odd-even carbon predominance, bacterially derived fatty acids (C14, C15, iso- and unsaturated acids), n-alkan-2-ones, des-A-triterpenoid hydrocarbons, hopanoids and some steroid ketones indicate that intense microbial reworking of the organic matter has taken place in this depositional environment. The chemical and biochemical conversions of some cyclic alkenes to alkanes, such as tricyclic diterpenoids, tetracyclic terpenoids and steroid ketones, are also evident with depth. The dominance of C20 components in the diterpenoid hydrocarbons may reflect an oxidizing or reducing depositional condition.  相似文献   

12.
This paper is the continuation of the paper published in 1985, with the emphasis on the irregular components of natural gases from the Sichuan Basin—the isotopic compositions of C,H and S, the n-and iso-alkane predominance (C6-C13) of methane homologues, the compositional characteristics of benzene and methylbenzene, and the distribution and geochemical characteristics of organic sulfur-bearing compounds including thiophen, thio-alcohol, etc. It is considered that natural gases from the Sichuan Basin have different distributional characteristics in different layers and locations, suggesting that they are controlled by a combination of factors such as kerogen type, maturity of organic matter and wall-rock assemblage.
  1. The type of source material (or precursor) is a main factor affecting the geochemical characteristics of natural gases. T3x-h and P2l produce coal-series gases with type-III source material dominant. The C and H isotopic compositions of natural gases are heavier, the contents of C6H6 and C7H8 are high, C7H8/C6H6 < 1. the content of C4H4S is low, and the predominance in isoalkane (C6C13) is obvious. J1t. P1y. Z2b. etc. produce oil-series gases with type-I and -II kerogens dominant, indicating that the geochemical characteristics of natural gases are different from those described above.
  2. The maturity of organic matter is an important factor affecting the composition of natural gases.With increasing maturity of organic matter, the C and H isotopic compositions tend to become light. C1 and C2 isotopic values are nearly equal or even inverse, and C4H4S decreases in content.
  3. Wall-rock assemblage has apparent influence on the S isotopic composition. The Middle-Lower Triassic series belongs to sulfate-carbonate formations enriched in gypsum. Therefore, the (δ34S values of natural gases are relatively high (< 20 %.) against the lower values for other layers due to the absence of gypsum layers.
  相似文献   

13.
The concentrations of polar organic compounds including n-alkanoic acids, n-alkanols, steroids and triterpenoids were determined in extracts of shallow sediments from the Mesopotamian marshlands of Iraq. The sediments were collected by a stainless steel sediment corer, extracted with a dichloromethane and methanol mixture (3:1 v:v) by ultrasonic agitation and then analyzed by gas chromatography–mass spectrometric (GC–MS). The analysis results showed that the n-alkanoic acids ranged from C8 to C20 with concentrations of 7.8 ± 1.2 μg/g sample, whereas the concentrations of n-alkanols, which ranged from C12 to C39 were from 28.6 ± 4.3 to 121.7 ± 18.3 μg/g sample. The steroids and triterpenoids included stenols, stanols, stenones, stanones, tetrahymanol, tetrahymanone and extended ββ-hopanes. The total concentrations of steroids and triterpenoids ranged from 26.8 ± 4.1 to 174.6 ± 26.2 μg/g and from 0.74 ± 0.11 to 11.2 ± 1.7 μg/g sample, respectively. The major sources of these lipids were from natural vegetation, microbial (plankton) residues and bacteria in the sediments, with some contribution from anthropogenic sources (livestock, sewage and petroleum). Further studies of these wetlands are needed to characterize the input rate, transformation and diagenesis of the organic matter and to assess its various sources.  相似文献   

14.
The current geochemical study of n-alkanes, steranes, and triterpanes in bitumen from the Late Maastrichtian–Paleocene El Haria organic-rich facies in West of Gafsa, southern Tunisia, was performed in order to characterize with accuracy their geochemical pattern. The type of organic matter as deduced from n-alkanes, steranes, and triterpanes distributions is type II/III mixed oil/gas prone organic matter. Isoprenoids and biomarkers maturity parameters (i.e., T s/T m, 22S/(22S?+?22R) of the C31 αβ-hopanes ratios, 20S/(20R?+?20S) and ββ/(ββ?+?αα) of C29 steranes), revel that the organic-rich facies were deposited during enhanced anoxic conditions in southern Tunisa. The organic matter is placed prior to the peak stage of the conventional oil window (end of diagenesis–beginning of catagenesis). All these result are suggested by total organic carbon analysis, bitumen extraction and liquid chromatography data. Thus, the n-alkanes, triterpane, and steranes study remains valuable and practical for geochemical characterization of sedimentary organic matter.  相似文献   

15.
A Pliocene oil shale (Pula, Hungary), a C3 plant Triticum aestivum and a C4 plant Zea mays were compared using isotopic composition of bulk organic matter, along with distributions and individual carbon isotope ratios of n-alkanes from organic extracts. The microalga Botryococcus braunii (A race) was thus shown to be the main source of the predominant 27, 29 and 31 n-alkanes of Pula sediment Therefore, the dominance of odd carbon-numbered n-alkanes in the range C25–35 in extracts from immature sediments shall not be systematically assigned to higher plant contribution but algal input is also possible. In fact, the long chain n-alkanes with an odd predominance previously observed in extracts of various immature sediments are likely to be derived at least partially, from algae.  相似文献   

16.
This new study was carried out in order to accurately characterize the geochemical pattern of Ousselat organic-rich facies from the Ypresian basin in central-northern Tunisia. It has been found that the organic matter is located towards the end of diagenesis/beginning of catagenesis. This assumption is supported by the relative low T max values (429–439°C) and by steranes maturity parameters such as C29 αα 20S/(20S + 20R), and C29 ββ/(ββ + αα). High HI values and the abundance of saturates (1–83%) compared to aromatics (2–27%) are unequivocal evidence of type-II organic matter as indicated by a high abundance of cholestane and the predominance of short-chain n-alkanes centred at n-C18 and at n-C20. Total organic carbon (TOC) content and petroleum potential values suggest that the Ypresian period corresponds to an anoxic event which led to the accumulation and preservation of large quantities of organic matter with high primary production. Due to their geochemical characteristics, the Lower Eocene facies represent a new potential source rocks in central-northern Tunisia.  相似文献   

17.
Modern sediments of Mono Lake show marked variation in lipid composition with depositional environment. Constituents derived from the drainage basin, characterized by high molecular weight alkane hydrocarbons (C25–C31), and the steroids β-sitosterol and brassicasterol, predominate in near-shore environments. In the deepest part of the lake, sediments exhibit a combination of externally-derived constituents, and lipids derived from the lake biota; the latter characterized by low molecular-weight alkanes and alkenes (C15–C17), phytane, and the steroids ergost-7-en-3β-ol and 24-ethylcholest-7-en-3-β-ol. Steranes, 4-methylsteranes, and the C18 and C19 isoprenoids appear to be forming in the intensely reducing bottom sediments at the present time.The compositions of samples from the Pleistocene succession of Mono Basin suggest that sample-to-sample variation within the same stratum is negligible so long as unweathered samples from the same depositional environment are compared. Sediments having equivalent lithologies may or may not have similar compositions, but sediments having similar fossil contents do show similar lipid compositions. Subaerial weathering of sediments causes a marked decrease in the amount of extractable organic material, as well as distinct changes in its hydrocarbon composition. Specifically, weathered sediments exhibit a decrease in relative content of low molecular weight hydrocarbons and a relative increase in nC22.Organic composition of sediments from the Pleistocene stratigraphie column cannot be correlated with depth of burial. Compositional changes with stratigraphie position are probably related to paleo-ecological factors such as population or productivity rather than depth of burial. Lithology and organic composition provide mutually-corroborating evidence regarding glacial advances in the adjacent Sierra Nevada Mountains. During glaciations, the lake sediments are rich in sandstones, and the organic composition shows a predominance of externally-derived debris, with no evidence for contributions from the lake biota.  相似文献   

18.
Coal beds of the Upper Cretaceous Fruitland Formation in the San Juan Basin of northwestern New Mexico and southwestern Colorado have significant liquid hydrocarbon generation potential as indicated by typical Rock-Eval Hydrogen Indexes in the range of 200–400 mg hydrocarbon/g organic carbon (type II and III organic matter). Small, non-commercial quantities of oil have been produced from the coal beds at several locations. The oils are characterized by high pristane/phytane (ca 4) and pristane/n-C17 ratios (ca 1.2), abundant C21+ alkanes in the C10+ fraction with a slight predominance of odd carbon-numbered n-alkanes, abundant branched-chain alkanes in the C15+ region, and a predominance of methylcyclohexane in the C4----C10 fraction. The oils are indigenous to the Fruitland Formation coals and probably migrated at thermal maturities corresponding to vitrinite reflectance values in the range 0.7–0.8%. Although the oils found to date are not present in commercial amounts, these findings illustrate the potential of some coals to generate and expel oil under conditions of moderate thermal heating.  相似文献   

19.
Stepwise pyrolysis-gas chromatography is used to examine and characterize the carbonaceous matter in sedimentary rocks. Low-temperature steps remove material normally volatile or extracted by benzene-methanol. Successively-higher temperature steps degrade the insoluble carbonaceous matter (kerogen) into smaller molecular pieces. The sequential pyrolysis steps have the advantage of breaking the kerogen at several temperatures which may be related to bond type or strength. The pyrolysis product chromatograms from each step can be compared. The molecular sizes (chain length) of kerogens fragments can be determined. The results presented here show the molecules in the range C11 to C23 because: (1) they can be compared to normal petroleum source rock extractables; and (2) these large molecules give a feeling for the molecular construction of the kerogen.Green River and Antrim shales show low-temperature material which is indigenous and not modified compared to the pyrolyzed kerogen fragments in the range C11C23. Kupferletten shows low-temperature material of a narrow molecular weight range of C15C19 which is probably derived from the kerogen. Monterey shale low-temperature material appears to be unrelated to the kerogen as represented by its pyrolysis products. The Pierre shale kerogen shows molecules over the range C11C23. Kerogen from the Romney shale has no molecules large than C8 in its pyrolysis products and no petroleum potential due to thermal and tectonic diagenesis.  相似文献   

20.
Agricultural soils are regarded as one potential sink for atmospheric CO2 via photosynthetic fixation in plant biomass and subsequent transformation into soil organic matter upon soil diagenesis. The difference in C-isotope signatures of C3- vs. C4-plants allows for a natural isotopic labelling of soil organic matter after changes from C3- to C4-cropping. In this study, we demonstrate that isotopic shifts are paralleled by molecular signatures of C3- vs. C4-crop alkyl lipids. Turnover times vary significantly, based on cropping techniques. For grain-maize cropped soils at steady state average turnover times of 40 years for bulk SOC, 35 years for n-alkanes and 21 years for n-carboxylic acids were determined. Turnover times for silage-maize cropped soil at steady state were on average 250 years for bulk SOC, 60 years for n-alkanes and 49 years for n-carboxylic acids. Turnover times reported here for silage-maize cropped soils may be taken as maximum values only, because they derive from a single trial, which was affected by addition of anthropogenic refractory carbon. Discrimination of input from various plant parts (roots, stems and leaves) based on bulk C-isotopes is not feasible but can easily be achieved using compositions of carboxylic acids, especially the ratio of n-C24 vs. n-C22+26 and their respective C-isotope values. This enables delineation of the influence of different cropping techniques, e.g., silage- or grain-maize, on carbon storage in soils. Admixture of external sources of organic matter to the soil organic carbon pool of an urban site in Halle, Germany was identified based on alkyl lipid distributions. Nearby lignite mining was identified as a source for non-crop-derived alkyl lipids, primarily based on the elevated n-C26-carboxylic acid content and heavier carbon isotopic signatures.  相似文献   

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