Organic matter in Silurian rocks from the Chernov uplift

This study presents data on the composition of organic matter from the Late Silurian sediments of the Chernov uplift. These sediments are characterized by low C_org contents, which may reach 1–3% in individual layers. A relatively high thermal maturity of organic matter is confirmed by polycyclic biomarker distributions and Rock-Eval pyrolyisis data. Despite its higher thermal maturity level (T _max = 456°C), kerogen in carbonaceous shales from the Padymeityvis River exhibits good preservation of long-chain n-alkyl structures, which are readily identified in the ¹³C NMR spectra and by the molecular analysis of the kerogen pyrolysis products.     

Biomarker geochemistry of marine organic matter in the Hushan and Chaohu areas,Lower Yangtze region

Marine strata are widely exposed in the Hushan and Chaohu areas, Lower Yangtze region. As biomarker geochemistry of the strata has not been well documented, this paper deals with the biomarker composition of representative samples collected from the Silurian, Carboniferous and Triassic systems and their geological implications, thus providing clues to marine organic matter. On the basis of experimental results, it is shown that abundant biomarkers (e.g. n-alkanes, isoprenoids, terpanes and steranes) were detected. As organic matter in the strata is highly to over mature in general based on petrologic microobservation, some biomarkers (mainly n-alkanes) except terpanes and steranes cannot reflect the source, depositional environment and maturity of organic matter. Thus, primarily based on analyses of the terpanes and steranes, it is suggested that organic matter in the Silurian and Carboniferous strata is derived mainly from lower organisms, while higher plants are predominant in the Triassic organic matter. This further indicates that the depositional environment may have transformed from the marine to continental facies in the Late Triassic. These results provide new evidence for the study of regional depositional evolution, and have enriched the study of biological composition of organic matter. In addition, the biomarker geochemistry of organic matter at high to over maturation stage is addressed.     

Organic matter in a low productivity anoxic intraplatform basin in the Triassic Tethys

This paper presents isotopic, bulk geochemical and biomarker data measured on organic matter accumulated in a narrow extensional basin developed at the oceanward margin of the huge Triassic carbonate platform in the Alps–Appenines domain. The integration of isotope signatures, organic petrographical and biomarker evidence together with the composition of kerogen pyrolysates suggests immature organic matter predominantly of algal origin with a minor, but not negligible, higher plant derived and moderate bacterial contribution for the entire sequence. The mineral sources are dominated by platform-derived subtidal Dachstein limestone with a minor palaeosol input and a moderate contribution of autochtonous quartz. Nevertheless, parallel variations observed in the mineral content, as well as in the amount and the quality of the organic matter reflect variations in the palaeoenvironment. The increased humidity, existing in the period of the accumulation of the upper section of the sequence, led to the restriction of dolomitization. A slightly greater higher plant derived contribution, in this section, is evidenced by the composition of bitumen and the results on GC and GC/MS analyses on the non-aromatic hydrocarbon fraction of bitumen. Moreover, the climate-induced weathering enchanced the primary productivity and resulted in a pronounced increase in the TOC content. The average estimated value of the planktonic productivity is about three times higher for the calcite-rich sequence than the dolomite-rich one, being 44.2 and 15.3 tC_org/m²/Ma, respectively. The low to moderate planktonic productivity shows that anoxic conditions, observed for the entire succession, are a consequence of the stagnant water stratification rather than high planktonic productivity. Depth trends in the data measured on kerogens (HI, OI, δ¹³Corg values, composition of pyrolysate) together with the δ¹⁸O excursions and Δδ¹³C values appear to be controlled by sea-level fluctuations. Consistent with the high abundance of alkyltiophenes in kerogen pyrolysates, the high S_org/C ratios (ranging between 0.05 and 0.10) suggest the importance of natural sulfurization in the formation of the sulfur-rich type-II-S kerogen occurring in all of the samples.     

Organic geochemical evidences of early-diagenetic oxidation of the terrestrial organic matter during the Triassic arid and semi arid climatic conditions

The molecular character of organic matter (OM) present in Triassic clays of the Upper Silesia Basin and NW border of the Holy Cross Mountains was determined using GC–MS analysis. Oxidation processes were the major cause of the main changes of extractable OM molecular composition during sedimentation and early diagenesis of the Triassic clays. They resulted in a very significant decrease in the OM content of the clays and transformation of n-alkanes, triterpanes and steranes. Despite the changes in biomarker composition resulting from the disappearance of unsaturated and ββ hopanes and dominance of αβ and βα hopanes as well as preponderance of αββ over ααα steranes, the aromatic ketones were identified. Such PACs as benzophenone, fluorenone, cyclopenta(def)phenanthrenone, antracenone and benzanthrone were among the compounds identified in the red clays. These commonly originate during oxidation of sedimentary organic matter. Moreover, the aromatic fraction is characterized by the presence of phenyl derivatives (phenylnaphthalenes, terphenyls, phenyldibenzofurans and phenylphenanthrenes) that are also products of the abiotic oxidation of organic matter. Periods of terrestrial sedimentation have been interrupted by long phases of OM weathering and oxidation during arid conditions, and OM might only have survived without significant oxidation changes when the sedimentation was fast and/or long-lasting.     

东海陆架盆地烃源岩及其烃类特点

东海陆架盆地自古新世至渐新世发育了四套含煤烃源岩与海相陆源有机质烃源岩,其有机质类型属腐殖型。在结构镜质体的细胞腔中普遍充填着生源为高等植物针叶林的树脂体,其含量在煤岩中最高可占全岩体积的8%。镜下还见到油珠及与树脂体有产状关系的渗出沥青体。受有机质类型的制约,液态烃中均检测到大量二萜类树脂化合物及倍半萜类化合物。由于这部分源干高等植物的化合物在饱和烃中占有相当比例,加上成烃后的运移效应,使原油具有“六低一高”的特点,即低比重、低含硫、低含蜡、低主峰碳位、低芳烃、低胶质(无沥青质)和高饱和烃,并具低成熟煤成烃特征。     

Lipid analysis of a ground sloth coprolite

Coprolites can provide detailed information about the nutritional habits and digestive processes of the animals that produced them and may also yield information about the palaeoenvironment in which the animal existed. To test the utility of the lipid biomarker approach to coprolite analysis, lipids were extracted from a coprolite of the Pleistocene ground sloth Nothrotheriops shastensis. Gas chromatography/mass spectrometry results revealed a dominant spiroketal sapogenin component identified, using nuclear magnetic resonance spectroscopy, as epismilagenin. The dominance of epismilagenin is probably due to ingestion of Yucca spp. and Agave spp., which is consistent with previous studies on the diet of this species.     

Micro-FTIR spectroscopy of liptinite macerals in coal

Reflectance FTIR microspectroscopy has been used to investigate the chemical structure of the liptinite macerals, alginite, bituminite, sporinite, cutinite and resinite in bituminous coals of Carboniferous to Tertiary age. In comparison with the spectra of vitrinite in the same coals, the micro-FTIR spectra of liptinite macerals are characterized by stronger aliphatic CH_x absorptions at 3000–2800 and 1460–1450 cm⁻¹, less intense aromatic C=C ring stretching vibration and aromatic CH out of plane deformation at 1610–1560 and 900–700 cm⁻¹ respectively and various intense acid C=O group absorptions at 1740–1700 cm⁻¹. The peaks at 1000–900 cm⁻¹ due to aliphatic CH₂ wagging vibrations in olefins and at 730–720 cm⁻¹ due to CH₂ rocking vibration in long chain aliphatic substances ([CH₂]_n, n≥4), are characteristic of liptinite macerals. Collectively the micro-FTIR spectral characteristics indicate that liptinite is composed of greater numbers of long chain aliphatics, fewer aromatics and a broader range of oxygen-containing groups than other macerals. Marked differences exist in micro-FTIR spectra within the liptinite maceral group. Alginite has the strongest aliphatic and least aromatic absorptions followed by bituminite, resinite, cutinite and sporinite. The aliphatic components in alginite are the longest chained and least branched whereas those in sporinite are the shortest chained and most branched. Bituminite, resinite and cutinite are intermediate. Notable differences in micro-FTIR spectra of individual liptinite macerals, such as intensities and peak locations of aromatic C=C in alginite, C=O groups in bituminite and resinite and substituted aromatic CH and C–O–C groups in cutinite and sporinite, also exist, which are attributed to differences in depositional environments or biotaxonomy.     

Thermal maturity and hydrocarbon potential of the sedimentary succession from the Hecla field in Sverdrup Basin, Arctic Canada

The thermal maturity and source-rock potential of the Upper Palaeozoic and Mesozoic sediments in the Hecla field, Melville Island, Arctic Canada, have been studied using reflected-light microscopy and Rock-Eval pyrolysis. Approximately 250 polished whole-rock samples were examined and their reflectance (% R₀, random) measured. In addition, approximately 100 samples were subjected to Rock-Eval/TOC analyses.Hydrogen-rich organic matter in the Schei Point Group sediments is dominated by alginite (Tasmanales), dinoflagellate cysts with minor amounts of sporinite, cutinite, resinite and liptodetrinite in an amorphous fluorescing matrix. Vitrinite reflectance in Cretaceous sediments ranges from 0.41 to 0.54%; in Jurassic sediments it ranges from 0.43 to 0.64% and in Triassic sediments from 0.50 to 0.65%. The Triassic Schei Point Group calcareous shales and marlstones contain organic matter mainly of marine origin, whereas the predominantly terrestially-derived organic matter present in the Jameson Bay (Lower Jurassic) and in the Upper Jurassic to Lower Cretaceous Deer Bay formations have ower TOC. Only the Ringnes Formation has a TOC content of equivalent to or greater than Schei Point source rocks. Within the Schei Point Group, the Cape Richards and Eden Bay members of the Hoyle Bay Formation are slightly richer in TOC than the Murray Harbour Formation (Cape Caledonia Member). Higher average TOC contents (>3.0%) have been reported in the Cape Richards and Eden Bay members in almost all Hecla drillholes.Variations in the level of thermal maturity of Mesozoic sediments in the Hecla field are a function of burial depth. The stratigraphic succession thickens towards the main Sverdrup Basin depocentre located in a N-NE direction. The pattern of the isoreflectance contours at the top of the Triassic (Barrow Formation) is similar to that of formation boundary lines of the same formations, an indication that present-day maturation levels are largely controlled by basin subsidence.     

A new approach to detecting vegetation and land-use change using high-resolution lipid biomarker records in stalagmites

A hundred-year stalagmite lipid biomarker record from Mechara, southeastern Ethiopia, is presented. The record has been recovered at a 10-yr temporal resolution, marking the first time this has been achieved in stalagmite biomarker work and providing the first opportunity to investigate the relationship between stalagmite lipid records and hydrological transport lags, a vital issue in interpreting palaeoenvironmental signals. Preserved plant-derived n-alkanes and n-alkanols show clear changes in composition over time, relating to known land-use changes in the area, particularly the expansion of agriculture in the early twentieth century. The level of environmental detail provided by this technique, combined with the long-term chronological framework offered by stalagmites, holds significant promise for the investigation of early human environments and their associated climatic and anthropogenic controls.     

Possible algal origin of long chain odd n-alkanes in immature sediments as revealed by distributions and carbon isotope ratios

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.     

Distribution of n-alkanes in lacustrine sediments from subtropical lake in Brazil

The geochemical composition of lake bed sediments of a tropical reservoir in Brazil have been investigated. The C, N, P composition showed almost no variation between the different sampling points. All samples contained inorganic phosphorus (IP) ranging from 52 to 70%. The Redfield ratios show that the lake is without significant anthropogenic inputs. Most of the organic matter is composed by higher plants decomposition revealed in the total organic carbon (TOC):nitrogen (N) ratio ranging from 15.4 to 57.2. Also, TOC:organic phosphorus (OP) ranged from 265.3 to 933.6, suggesting that most of the organic matter has terrestrial origin from wood plants. The ratios suggest that most organic matter is influenced by the terrestrial characteristics of the watershed. Furthermore, the relative abundance of n-alkane homologues in the sediments was investigated. All samples have been analyzed for the n-alkanes C₈ to C₄₀. The sediments were dominated by n-alkanes C₂₅–C₃₈. It is concluded that n-alkane in sediments mainly come from terrestrial plants, however there is a contribution of submerged aquatic plants, especially in those sites in deeper areas of the lake. On the basis of P_aq index the n-alkanes in sediments comes from terrestrial plants, however there is a contribution from emerged/floating plants.The investigated lake seems to be considered as meso to eutrophic. Because of the relatively high primary productivity in the lakes, there is a substantial organic-matter flux to the sediments, which rapidly becomes anoxic. According to the pristine/phytane ratio the sediments represent an anoxic environment with values found between 0.38 and 1.72.     

Hydrothermal bitumen generated from sedimentary organic matter of rift lakes – Lake Chapala, Citala Rift, western Mexico

Lake Chapala is in the Citala Rift of western Mexico, which in association with the Tepic-Zacoalco and Colima Rifts, form the well-known neotectonic Jalisco continental triple junction. The rifts are characterized by evidence for both paleo- and active hydrothermal activity. At the south shore of the lake, near the Los Gorgos sublacustrine hydrothermal field, there are two tar emanations that appear as small islands composed of solid, viscous and black bitumen. Aliquots of tar were analyzed by GC-MS and the mixtures are comprised of geologically mature biomarkers and an UCM. PAH and n-alkanes are not detectable. The biomarkers consist mainly of hopanes, gammacerane, tricyclic terpanes, carotane and its cracking products, steranes, and drimanes. The biomarker composition and bulk C isotope composition (δ¹³C = −21.4%) indicate an organic matter source from bacteria and algae, typical of lacustrine ecosystems. The overall composition of these tars indicates that they are hydrothermal petroleum formed from lacustrine organic matter in the deeper sediments of Lake Chapala exceeding 40 ka (¹⁴C) in age and then forced to the lakebed by tectonic activity. The absence of alkanes and the presence of an UCM with mature biomarkers are consistent with rapid hydrothermal oil generation and expulsion at temperatures of 200–250 °C. The occurrence of hydrothermal petroleum in continental rift systems is now well known and should be considered in future energy resource exploration in such regions.     

Composition of organic matter in subducted and unsubducted sediments off the Nicoya peninsula, Costa Rica (ODP Leg 170, Sites 1039 and 1040)

Investigation of sediment samples from Sites 1039 and 1040 (ODP Leg 170) drilled off the Nicoya peninsula (Costa Rica) by organic geochemical and organic petrological methods has revealed that subduction has only little influence on the composition of the sedimentary organic matter. Organic carbon contents reached 1.5% in the Pleistocene samples but Miocene and Pliocene sediments had an average organic carbon content of less than 0.5%. Organic carbon/sulfur ratios are generally below 2.8, reflecting an intense sulfate reduction in the uppermost sediments which was enhanced by sulfate supply both from sea water and deeper strata. Microscopical examinations indicate that the organic matter is mainly derived from marine sources. A small amount of terrigenous organic matter is, however, present as well according to n-alkane and fatty acid distributions. The alkenone unsaturation index U₃₇^k′ shows only a slight decrease during the Miocene and Pliocene, and stronger variations in the Pleistocene, probably indicating more stable sea surface temperatures during the Miocene and Pliocene. Variations in the Pleistocene can possibly be related to glacial/interglacial changes.     

New aromatic biomarkers and possible maturity indicators found in New Albany Shale extracts

Aromatic hydrocarbons from benzene extracts of New Albany Shale were characterized. A biomarker that has a molecular weight of 546 and a structural configuration consistent with that of an alkyl-aromatic hydrocarbon (C₄₀H₆₆) was tentatively identified. It was found that the relative concentrations of the biomarker are indicative of differing levels of thermal maturity of the shale organic matter. A 40-carbon bicyclic carotenoid (C₄₀H₄₈) is proposed as the geochemical precursor of this biomarker. Thermal maturity of the shale organic matter can also be differentiated by observing differences in “fingerprints” as obtained by field-ionization mass spectrometry on the aromatic hydrocarbon fraction. Using this technique, we found that the more mature shale samples from southeastern Illinois contain more low molecular weight extractable aromatic hydrocarbons and the less mature shale samples from northwestern Illinois contain more high molecular weight extractable aromatic hydrocarbons. It was demonstrated that field-ionization and tandem mass spectrometric techniques through fingerprint and individual compound identification, are useful for shale aromatic hydrocarbon fraction characterization and for thermal maturation interpretation.     

Diversities in biomarker compositions of Carboniferous–Permian humic coals in the Ordos Basin,China

The molecular composition of Carboniferous–Permian coals in the maturity range from 0.66 to 1.63% vitrinite reflectance has been analysed using organic geochemistry to investigate the factors influencing the biomarker compositions of humic coals. The Carboniferous–Permian coal has a variable organofacies and is mainly humic-prone. There is a significant difference in the distribution of saturated and aromatic hydrocarbons in these coals, which can be divided into three types. The Group A coals have biomarker compositions typical of humic coal, characterised by high Pr/Ph ratios, a lower abundance of tricyclic terpanes with a decreasing distribution from C₁₉ tricyclic terpane to C₂₄ tricyclic terpane and a high number of terrigenous-related biomarkers, such as C₂₄ tetracyclic terpane and C₂₉ steranes. The biomarker composition of Group B coals, which were deposited in a suboxic environment, have a higher abundance of rearranged hopanes than observed in Group A coals. In contrast, in Group C coals, the Pr/Ph ratio is less than 1.0, and the sterane and terpane distributions are very different from those in groups A and B. Group C coals generally have abnormally abundant tricyclic terpanes with a normal distribution maximising at the C₂₃ peak; C₂₇ steranes predominates in the m/z 217 mass fragmentograms. The relationships between biomarker compositions, thermal maturity, Pr/Ph ratios and depositional environments, indicate that the biomarker compositions of Carboniferous–Permian coals in Ordos Basin are mainly related to their depositional environment. This leads to the conclusion that the biomarker compositions of groups A and B coals collected from Shanxi and Taiyuan formations in the northern Ordos Basin are mainly related to their marine–terrigenous transitional environment, whereas the biomarker compositions for the Group C coals from Carboniferous strata and Shanxi Formation in the eastern Ordos Basin are associated with marine incursions.     

<Emphasis Type="Italic">P</Emphasis>–<Emphasis Type="Italic">T</Emphasis> and fluid evolution of barren and lithium pegmatites from Vlastějovice,Bohemian Massif,Czech Republic

Fluid inclusions, mineral thermometry and stable isotope data from two types of mineralogically and texturally contrasting pegmatites, barren ones and lithium ones, from the Moldanubian Zone of the Bohemian Massif were studied in order to constrain P–T conditions of their emplacement, subsolidus hydrothermal evolution and to estimate composition of the early exsolved fluid and that of the parental melt. Despite the fact that the lithium pegmatites are abundant throughout the crystalline units of the Bohemian Massif, data similar to this paper have not been published yet. The studied pegmatites are hosted by iron-rich calcic skarn bodies. This specific setting allowed scavenging of calcium, fluorine and some other elements from the host rocks into the pegmatitic melts and post-magmatic fluids. Such contamination process was important namely in the case of barren pegmatites, as can be deduced from the variation in anorthite contents in plagioclase and from the presence of fluorite, hornblende (with F content) or garnet in the contact zones of pegmatite dykes. Fluid inclusions were studied mostly in quartz, but also in fluorite, titanite and apatite. Early aqueous–carbonic and late aqueous fluids were identified in both pegmatite types. The P–T conditions of crystallization as well as the detailed composition of exsolved magmatic fluid, however, particularly differ. The magmatic fluids associated with barren pegmatites correspond to H₂O–CO₂ low salinity fluids, composition of which evolved from 20 to 23 to <5 mol% CO₂, and from 2 to 4–6 mol% NaCl eq. Sudden decrease in the CO₂ content of the post-magmatic fluids (<5 mol% CO₂) seems to coincide with the enrichment of the fluid in calcium (from the contamination process) and resulted in precipitation of calcites (frequently found as trapped solid phases in fluid inclusions). The fluids associated with lithium pegmatites are more complex (H₂O–CO₂/N₂–H₃BO₃–NaCl). The CO₂ content of early exsolved fluid is 26–20 mol% CO₂ and remains the same in the next fluid generation. The main difference between the magmatic and the first post-magmatic fluids is the presence of 7–9 wt% of H₃BO₃ (identified as daughter mineral sassolite) in the former. The second post-magmatic fluids are again CO₂-poor (∼4 mol%) and more saline (∼4 mol% NaCl eq.). The composition of exsolved fluid was further used to constrain volatile composition and content of the parental melts. Finally, P–T conditions of pegmatite crystallization are constrained: 600–640°C and 420–580 MPa for the barren pegmatites and 500–570°C and 310–430 MPa for the lithium pegmatite. While the emplacement of the former occurred in thermal equilibrium with the Moldanubian host rock environment, the emplacement of the later suggests substantial thermal disequilibrium.     

Observations on Indian Permian Gondwana Coals Under Fluorescence Microscopy: An Overview

Macerals like sporinite, cutinite, suberinite and resinite of the liptinite group have been insufficiently recorded in Indian Permian Gondwana coals, until the fluorescence microscopy came into existence. With the introduction of this technique, macerals like bituminite, fluorinite and exsudatinite were convincingly recognized and alginite and liptodetrinite, normally mistaken for mineral matter under normal reflected light in routine coal petrographic analysis, were identified with certainty. Thus, fluorescence microscopy has added certain new macerals to the tally of the liptinite group and has increased their overall proportion in Indian Gondwana coals.In addition to the liptinite group, collodetrinite (=desmocollinite) and a certain fraction of collotelinite (=telocollinite) macerals of the vitrinite group were found to be fluorescing with dull reddish-brown to dark brown colours. Certain semifusinite and inertodetrinite macerals of inertinite group were also found to fluoresce with almost identical intensity and colour as that of the associated perhydrous (fluorescing) vitrinite. Contributions of degraded resinite, algal matter and bitumen in the formation of perhydrous vitrinite have been established. The fluorescence behaviour of inertinite appears to be related with its genesis from partial oxidation of resin/bitumen-impregnated cell walls.     

Tmax of asphaltenes: a parameter for oil maturity assessment

A new maturity parameter determined on both oil and bitumen samples, the asphaltene T_max, is proposed and discussed. This parameter could be very useful to address the maturity of the source rock. The asphaltene T_max is measured by programmed Rock-Eval pyrolysis, using a modified temperature program. Some phases of the experimental procedure, such as the asphaltene preparation and the Rock-Eval measurement substratum choice, are crucial in order to achieve reliable data. Laboratory simulations were carried out in order to assess the possible effects of both primary and secondary migration on asphaltene T_maxin the expelled oil: the original value of the asphaltene T_max in the bitumen is not substantially modified and it is very close to that measured on kerogen. Examples of the determination of asphaltene T_max on many samples, collected from different areas and with different organic matter composition, are given. Results show that T_max values from oil asphaltenes are reasonable indicators of source rock maturity.     

Genesis of Oils in Eastern Kamchatka: Evidence from Hydrocarbon Biomarkers

Gas chromatography and gas chromatography–mass spectrometry data on oils from wells and seeps in the Eastern Kamchatka Basin indicate that, according to their composition and the distributions of biomarker molecules, these oils can be classified into three groups, which differ in the composition of the parent organic matter, litho–facies sedimentation conditions, and catagenetic transformations. Oils from the wells were determined to be produced by organic matter of the sapropel type of marine facies in the main oil window (MC₂). Condensate from the natural seep was generated at higher catagenesis grades (MC_2–3) by organic matter of the sapropel–humus type of littoral facies. Uzon oil shows are demonstrated to be formed in a continental environment by organic matter of the humus–sapropel type and were not genetically related to oil from the Paleogene–Neogene source rocks of the Bogachevka Formation.     

Biogeochemistry of high salinity microbial mats – Part 1: Lipid composition of microbial mats across intertidal flats of Abu Dhabi, United Arab Emirates

As a contribution to a project on the role of aerobic heterotrophic bacteria in the organic matter turnover within cyanobacterial mats, we investigated selected lipid classes of five morphologically different microbial mats from the intertidal area of Abu Dhabi, United Arab Emirates. The mats thrive under extreme environmental conditions as they are exposed to salinity up to 200 and shadowless sunshine for nearly 12 h per day. The total extractable organic matter is characterised by heavy δ¹³C values of −17‰ to −10‰, suggesting CO₂ limitation. The lipids reflect the biomass of the principal mat-building phototrophic and heterotrophic microorganisms. Moderate amounts of hydrocarbons, mainly cyanobacterial n-heptadecane, short chain monomethyl alkanes and diploptene were detected in all the mats. The ubiquitous n-hexadecanoic acid is dominant amongst the free and ester-bound phospholipid fatty acids (PLFAs), whereas the overall acid composition varies due to differences in the extreme environmental conditions. Additionally, the top layers of two of the five mats were analysed separately to compare their lipid compositions with those of the whole mats. As would be expected, the concentrations of cyanobacterial biomarkers exceed those found in the total mats. Noteworthy is the presence of n-heneicosadiene as predominant hydrocarbon in the top layer of the so called gelatinous mat, which thrives under the locally most extreme conditions. As the n-alkadiene was present to a much lesser extent in the intact mat, it may provide a new biomarker for a so far unknown important aerobic organism.