Sterols of a contemporary lacustrine sediment

C₂₆, C₂₇, C₂₈ and C₂₉ sterols, including Δ⁵-, Δ²²- and Δ^5,22-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.     

Sterols in interstitial waters of marine sediments

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.     

Sterol Distribution in Sediments from Chaiwobu Lake and Caohai Basin and Its Geochemical Significance

In order to understand the distribution characteristics of biomarkers in source rocks,which may be related to organic input,Quaternary sediments from the Caohai Basin and the Chaiwobu Lake were analyzed for sterols,As a result,various sterols,have been found in the sediments.The composition of sterols in the sediments revealed that cholesterols and cholestadienols are more abundant than their C29 counterparts in the Chaiwobu Lake sediments and that C29 sterols are more abundant in the peats from the Caohai Basin,It is also found that stanol/sterol ratios in clays are higher than in peats.Studies show that organic input to the Chaiwobu Lake is mainly plankton and zooplankton and to the Caohai Basin is mainly terrestrial high plant.The authors have proposed that the relative abundance of C27 or C29 sterane in source rocks may reflect input characteristics to some extent and the stanol/sterol ratios may reflect the redox conditions of the depositional environments.     

Esters of acyclic and polycyclic isoprenoid alcohols: Biochemical markers in lacustrine sediments

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.     

5α(H)-cholestan-3α-ol in sediments: Characterization and geochemical significance

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.     

Fecal Sterols in Estuarine Sediments as Markers of Sewage Contamination in the Cubat?o Area, S?o Paulo, Brazil

Sterol biomarkers serve as an alternative method for detecting sewage pollution. Sterols were extracted from samples of surface sediment collected in Cubat?o (the Vila dos Pescadores and Vila Esperan?a communities) and quantified using GC–MS after Soxhlet extraction, cleanup, and derivatization. Fecal contamination was evaluated based on the concentration of coprostanol and the ratio of the selected sterols. The most abundant sterol was cholestanol, followed by coprostanol. The concentrations of coprostanol in surface sediments ranged from a minimum of 4.21?μg?g^?1 dry sediment (Vila dos Pescadores station) to a maximum of 8.32?μg?g^?1 dry sediment (Vila Esperan?a station). A coprostanol concentration of about 10?μg?g^?1 was found, indicating areas of high sewage contamination. Coprostanol levels at sewage stations were higher than in other Brazilian coastal areas, which may be attributed to the fraction of the population without sanitation services.     

Sources of neutral lipids in a temperate intertidal sediment

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.     

The geochemical significance in early sedimentation of geolipids obtained by saponification of lacustrine sediments

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 ($\text{δ}{}^{13}\text{C}$) 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.     

青海湖沉积物中的甾醇及其演化

Ｃ_２７，Ｃ_２８和Ｃ_２９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Ｃ_２９甾醇占优势。在ＱＥ和ＱＧ孔沉积物中还检出了低浓度的三个Ｃ_３０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，Ｃ_２７，Ｃ_２９.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。     

Vertical transport of steroid alcohols and ketones measured in a sediment trap experiment in the equatorial Atlantic Ocean

The vertical flux and free steroid alcohol (sterol) and ketone composition of particulate material was determined using sediment traps deployed at 389, 988, 3755 and 5068 m at a station in the equatorial North Atlantic, PARFLUX E. Cholest-5-en-3β-ol (cholesterol) was found to be the dominant sterol in all the traps. This compound had a maximum flux at 988 m, accounting for more than 90% of the sterols at this depth. Inputs from mesopelagic Zooplankton populations living in or migrating to depths between the 389 and 988 m traps appear to be responsible for this distribution. The deeper two traps exhibited an increased flux of phytosterols relative to cholesterol, probably due to (a) the incorporation of labile phytoplankton remains in fecal pellets and rapid transport into the deep sea and (b) differential dissolution of heterogeneous large particles. A maximum of 5–22% of the sterols produced in the euphotic zone were present in the 389 m trap. This value drops to less than 1% for the 5068 m trap, 200 m above the sediment surface.In general steroid ketone fluxes gradually decreased with depth. Δ4-Stenones were found in greater abundance than their saturated counterparts. Cholest-4-en-3-one was the major steroid ketone detected in all the traps. A five-fold increase with depth in the cholest-4-en-3-one to cholesterol ratio is most likely due to microbial oxidation of sterols to steroid ketones, or higher Δ4-stenone inputs relative to sterols from organisms.     

Free and bound lipids in recent (1835–1987) sediments from Santa Barbara Basin

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.     

Occurrence of Different Forms and Implications of Compound Specific Sterols in Continental Sediments of the Northeast South China Sea

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.     

Diatoms as a source for 4-desmethyl-23,24-dimethyl steroids in sediments and petroleum

Analysis of the sterol composition of more than 100 diatom cultures, representing all major marine diatom orders, indicates that this group of algae may be an important source for 4-desmethyl-23,24-dimethyl steroids in sediments and petroleum, as their precursors, i.e. 4-desmethyl-23,24-dimethyl sterols, were present in 22 of the cultures. The phylogenetic positions of diatom species that produce 4-desmethyl-23,24-dimethyl sterols show that, within the centric diatoms, only a specific group of diatoms is able to produce these sterols, while within the pennate diatoms, a phylogenetic relationship between 4-desmethyl-23,24-dimethyl sterol-producing diatoms is less apparent. Based on the phylogenetic relationship, it is suggested that diatoms inherited the ability of producing these sterols from a single common ancestor, which originated between 150 and 100 Ma ago. Co-injection of an authentic 23R,24R-dimethyl-5α-cholestane standard with extracts confirmed its presence in sediments. We also tentatively identified three other 4-desmethyl-23,24-dimethyl sterane isomers having different side-chain stereo-configurations and observed that some of the isomers co-elute with other steranes including 24-ethyl-5α-cholestane.     

Combined organic and inorganic geochemical reconstruction of paleodepositional conditions of a Pliocene sapropel from the eastern Mediterranean Sea

Layers of organic-carbon-rich sapropels in the sediment record of the Mediterranean Sea give evidence of repetitive changes in regional Plio-Pleistocene climate. Results from biomarker molecule and major and trace element analyses of closely spaced samples are used to reconstruct the conditions leading to deposition of a Pliocene sapropel at Ocean Drilling Program (ODP) Site 969 on the Mediterranean Ridge. Organic carbon concentrations increase from 0.2% outside the sapropel and peak to more than 30% within it. Major and trace elemental composition and biomarker-derived parameters indicate elevated productivity, depletion of water-column dissolved-oxygen content, and changes in sediment provenance in response to climatic changes. Budgets of rhenium, thallium, and other trace metals indicate that deep-water exchange between the Mediterranean subbasins and the Atlantic Ocean was not completely interrupted during sapropel formation. Enrichment factors of redox-sensitive and sulfide-forming trace metals as well as the presence of isorenieratene derivatives and high stanol/sterol ratios point to an extended zone of anoxic water masses. Depth profiles of biomarker compositions (sterols, long-chain alkenones, alkandiols and -ketols, fatty acids) indicate great floral diversity during deposition of a single sapropel and highlight the sensitive response of the marine community to variable environmental conditions. Changes in water mass circulation and eolian transport can be reconstructed by use of both lithogenic elements and average chain lengths of n-alkanes (ACL index).     

Anomalies in steroid and hopanoid maturity indices

The purpose of this letter is to put forward new interpretations of published data relating to ancient hypersaline environments.Recent hypersaline environments are often characterized by high amounts of relatively uncommon sterols, such as Δ⁷ sterols. The diagenetic pathway of such sterols, tentatively proposed here, might “rapidly” lead to formation of 20R- and 20S-5α(H),14β(H),17β(H)-steranes, providing such immature samples with a “mature appearance.” Extended 17α(H),21β(H)-hopanes and extended hop-17(21)-enes, present in ancient hypersaline environments, occur fully isomerized at C-22 and a diagenetic pathway explaining this phenomenon is proposed. The use of these specific stereoisomers as maturity parameters in the reconstruction of the thermal and burial history of sediments, could therefore lead to erroneous conclusions.     

Molecular evidence for recent land use change from a swampy environment to a pond (Lorraine,France)

Evidence of a changing environment in the catchment area of a small pond (Lansquenet, Lorraine, France) during the last millennium was provided by coupling palynology data and organic ratios [terrestrial to aquatic ratio: TAR_(HC); the C₂₉ vs. C₂₇ sterols, C₂₉/C_27(ST); average chain length, ACL and aquatic/macrophytes ratio, P_aq]. The depositional and alteration conditions of organic matter (OM) were provided by the 5α(H)-stanols/Δ⁵-sterols ratio. This study shows that quite simple organic ratios clearly allow identification of the different evolution steps of a watershed, from a swamp to the progressive settlement of a pond. During the swampy period, the C/N_(at) (ca. 11.1), TAR_(HC) (ca. 36.8)_, C₂₉/C_27(ST) (ca. 8.7) and P_aq (<0.3) show a high contribution of allochthonous OM associated with the presence of particular aquatic and mesohygrophilous species. A woody level dated to the XIIIth century reflects the period of the settlement of the pond in a more oxic environment [5α(H)-stanol/Δ⁵sterol ratio <0.2]. Then, the progressive increase in aquatic input and the development of submerged and floating macrophytes are evidenced by low C/N_(at) (<7.6), TAR_(HC) (ca. 2.7), C₂₉/C_27(ST) (ca. 2) and high P_aq (ca. 0.5), suggesting an increase in the water level and eutrophication of the pond. A second oxic event [5α(H)-stanols/Δ⁵sterols ratio averaging 0.16], associated with extensive OM degradation, corresponds to the most recent dredging in 2002 and reflects an important disturbance of sediments due to pond management.     

Stenols and stanols in the oxic and anoxic waters of the Black Sea

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 $\text{O}{}_2\text{H}{}_2\text{S}$ 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 $\text{O}{}_2\text{H}{}_2\text{S}$ 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 $\text{O}{}_2\text{H}{}_2\text{S}$ 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 $\text{O}{}_2\text{H}{}_2\text{S}$ interface or in the deep anoxic waters of the Black Sea.     

Spectroscopic and Chromatographic studies of organic carbon in Recent marine sediments from the Peruvian Upwelling Zone

Early diagenesis of organic matter in sediments from two sites in the Peruvian Upwelling Zone (12°05′S, 77°39′W; 15°17′S, 75°24′W) has been studied by observing changes in the total organic carbon and lipid and humin fractions with depth. Transformations of the total carbon and humin fraction have been characterized by conventional and time-dependent solid state NMR techniques, while lipid diagenesis was monitored by measuring the concentration of sterols in the same sedimentary horizons. Both the quantity of total sterols and the relative abundances of individual sterols vary with sampling location, suggesting a difference in the input of biomass to the sediments at the two sites. Total sterol concentrations decrease with depth at both sites, but the loss of sterols occurs much more slowly at the more anoxic northern site, where sedimentation rates and organic carbon contents are approximately twice those at the southern site. ¹³C-NMR spectra of the total organic carbon and the humin fraction suggest that humin-like compounds are an original component of the sedimentary biomass, and dipolar-dephased spectra of the humin residue indicate that diagenetic alterations of the humin fraction are occurring even in these very young sediments. Conventional and time-dependent spectroscopic data support the hypothesis that humin formation results from selective preservation of microbially-resistant biopolymers which are an original component of the sedimentary biomass combined with loss of certain labile compounds.     

Several unexpected marine sterols in a freshwater sediment

Some unexpected stanols, 22,23-methylene-23,24-dimethyl-5α(H)-cholestan-3β-ol (gorgostanol and the related stenol), 24,26-dimethyl-5α(H)-cholestan-3β-ol (aplystanol) and most probably 24-isopropyl-5α(H)-cholest-22-en-3β-ol, have been found in the sediment of a eutrophic pond. These compounds possess side chains which have until now been considered to belong exclusively to sterols of marine origin. The presence of these stanols in a freshwater sediment suggests that considering their side chain structures as specific marine input markers can lead to erroneous conclusions. The vertical distribution of these compounds along a 6 m core shows that they arise from organisms which still exist except for aplystanol which was found only in the sections below 5 m.     

The occurrence of stanols in various living organisms and the behavior of sterols in contemporary sediments

Unsaturated sterols (stenols) and saturated sterols (stanols) in phytoplankton and Zooplankton from Lake Suwa and from higher plants around the lake were analyzed by combined GLC and MS. In all the organisms investigated, 5α-cholestanol, 24-methylcholestan-3β-ol and 24-ethyl-5α-cholestanol were found, although in low concentrations, together with large quantities of stenols. This strongly suggests the contribution of stanols from living organisms to recent sediments.Findings from incubation experiments of cholesterol and 5α-cholestanol in the surface sediment from Lake Suwa extending through 450 days suggest the following: (1) stanols are slowly degraded and tend to survive unaltered in sediments in comparison with stenols, (2) in a relatively oxidative depositional environment such as Lake Suwa, the greater part of the stanols in the surface sediment originates from living organisms, (3) the reduction zone in which the degradation of sterols is suppressed and the rapid hydrogenation of stenols takes place may be in the microbiologically active sediment from 1 cm to about 10 cm in Lake Suwa, and (4) the increase in the ratio of stanols to stenols with depth below the zone may be caused by the simultaneous progress of preferential degradation and slow hydrogenation of stenols during long-term preservation in sediments.