A chemical investigation of the transport and fate of petroleum hydrocarbons in littoral and benthic environments: The TSESIS oil spill

The fate of saturated and aromatic hydrocarbons discharged into the coastal Baltic Sea environment from the TSESIS oil spill has been studied in the acute and postacute (one year) phases of the spill. Periodic samples of Mytilus edulis (mussels) from eight littoral zone stations and Macoma balthica from nine soft bottom stations were obtained as well as sediment trap samples and surface sediment samples. Glass capillary gas chromatography and gas chromatographic mass spectrometry were used as the analytical tools to determine saturated and aromatic hydrocarbon composition and concentrations in these samples.Sediment trap samples indicated that sizable quantities of chemically and microbially weathered oil were sedimented, and available for benthic uptake shortly after the spill. After initial uptake of sedimented oil (500 to 1000 μ/g dry weight), Macoma populations appear to have begun slow depuration through the first winter after the spill, but TSESIS oil was again introduced to the benthic stations studied during the following summer. Mytilus populations in the region were severely impacted by the oil. Initial depuration of spilled oil during the first month was rapid and nearly complete at all but the most heavily impacted stations one year after the spill. The post-spill depuration of assimilated hydrocarbons was characterised by a relative retention of alkylated dibenzothiophenes and alkylated phenanthrenes compared to their unsubstituted parent compounds and compared with the entire homologous naphthalene series.These data suggest that petroleum hydrocarbons from the TSESIS spill have become a chronic source of degraded saturated and aromatic hydrocarbons to the soft bottom benthic communities. Petroleum hydrocarbons in the benthic environment from this spill appear to reside in the difficulty sampled and mobile flucculent layer at the sediment/water interface and may affect epifaunal communities for an extended period of time.     

Benzo[b]naphthothiophenes and alkyl dibenzothiophenes: Molecular tracers for oil migration distances

The secondary migration of petroleum is one of the most critical geological processes responsible for the accumulation of hydrocarbons in a sedimentary basin. Pyrrolic nitrogen compounds such as carbazoles and benzocarbazoles are thought to be practical molecular indicators for estimating relative migration distances of oil. In light oils or condensates, however, considerable analytical errors are usually caused by low concentrations of NSO-compounds. Here we show that polycyclic sulfur aromatic hydrocarbons such as dibenzothiophene, C₁∼C₃ alkylated dibenzothiophenes and benzo[b]naphthothiophenes, which are present in relatively higher concentrations than the pyrrolic nitrogen compounds, exhibit changes in both absolute and relative concentrations that correlate with migration distances. The polycyclic sulfur aromatic hydrocarbons related parameters — benzo[b]naphtho[2,1-d]thiophene/{benzo[b]naphtho[2,1-d]thiophene + benzo[b]naphtho[1,2-d]thiophene} (abbreviated as [2,1]BNT/([2,1]BNT+[1,2]BNT) and the concentration of total dibenzothiophenes plus benzo[b]naphthothiophenes — are proposed by this paper to trace the oil migration distances.     

Impact of crude oil on sulphate reduction and methane production in sediments impacted by the Amoco Cadiz oil spill

The activities of methane-producing and sulphate-reducing bacteria in intertidal sediments along the Brittany coast of France were examined in order to determine the effect of the Amoco Cadiz oil spill on sediment microbial processes. Porewater chemistry, methane production, sulphate rate and [2?¹⁴C]-acetate metabolism did not vary significantly between beach, estuary, and marsh sites, oiled or unoiled, after the Amoco Cadiz spill. Oiled sediments contained highly weathered oil of Amoco Cadiz origin, but unoiled comparison sites also contained hydrocarbons from anthropogenic sources. The additions of weathered Amoco Cadiz mousse, fresh and slightly weathered light Arabian crude oil, benzene or toluene to sediments from the oiled and unoiled marsh site did not significantly affect rates of sulphate reduction or methane production. The oxidation of [2?^14C]-acetate to ¹⁴CO₂, however, was significantly decreased when mousse, crude oil, benzene or toluene was added to sediments from the unoiled site. Inhibition seemed to be proportional to the extent of weathering. Sediments recently exposed to Amoco Cadiz crude oil were less affected by a second oiling, suggesting that the indigenous populations may have been replaced by organisms more resistant to oil toxicity. These results suggested that the Amoco Cadiz oil spill did not have major long-term effects on sulphate reduction or methane production.     

Hydrocarbons in the Surface Layer of Bottom Sediments in the Northwestern Caspian Sea

The paper presents research results on the concentrations and compositions of aliphatic and polycyclic aromatic hydrocarbons in the surface layer of bottom sediments in the Northwestern Caspian Sea (2014) and compares them to data for sediments of the Middle and Southern Caspian (2012–2013). The seepage of hydrocarbons out of the sediment mass, resulting in abnormally high concentrations of aliphatic hydrocarbons per dry weight (up to 468 μg/g), as well as within the C_org composition (up to 35.2%), is considered the main source of hydrocarbons in sediments in the surveyed area of the Northern Caspian. This is also confirmed by the absence of any correlation between the hydrocarbon and C_org distributions, as well as by the transformed oil composition of high-molecular alkanes. The distribution of markers within polycyclic aromatic hydrocarbons points to a mixed genesis—petrogenic and pyrogenic—with prevalence of the latter. Unlike the shallow-water northern part of the Caspian Sea, the content and composition of hydrocarbons in deep-seated sediments are affected by facial conditions of sedimentation and by matter exchange at the water–bottom interface. Therefore, despite high C_org concentrations (up to 9.9%), sediments in deep-water depressions are characterized by a quite low concentration of aliphatic hydrocarbons (52 μg/g on average; 0.2% of C_org) with prevailing natural allochthonous alkanes.     

The widespread occurrence of highly branched acyclic C20, C25 and C30 hydrocarbons in recent sediments and biota—A review

The occurrence of widely distributed acyclic isoprenoid hydrocarbons (C_2O, C₂₅ and C₃₀) with highly branched structures, in sediments and biota is reviewed. The compounds occur as alkanes and alkenes with from one to at least four double bonds in young aquatic (both marine and lacustrine) sediments from many parts of the globe (e.g. Peru, Antarctica, Gulf of Suez, North Sea, Atlantic) sometimes in high concentrations (e.g. 40 μg g⁻¹ sediment) relative to other hydrocarbons. However, the compounds rapidly disappear in older sediments, possibly due to biodegradation and reaction with sedimentary sulphur. These and other factors are discussed.The sources of this fascinating group of hydrocarbons remain largely unknown, though evidence points to algae (possibly diatoms) as one possibility. The recent identification of related sulphur-containing compounds in a crude oil promises to extend the number of reports of these compounds still further, and to increase their importance as environmental biological markers.     

Organic geochemistry of sediments from chemosynthetic communities,Gulf of Mexico slope

We used a research submersible to obtain 33 sediment samples from chemosynthetic communities at 541–650 m water depths in the Green Canyon (GC) area of the Gulf of Mexico slope. Sediment samples from beneath an isolated mat of H₂S-oxidizing bacteria at GC 234 contain oil (mean = 5650 ppm) and C₁–C₅ hydrocarbons (mean = 12,979 ppm) that are altered by bacterial oxidation. Control cores away from the mat contain lower concentrations of oil (mean = 2966 ppm) and C₁–C₅ hydrocarbons (mean = 83.6 ppm). Bacterial oxidation of hydrocarbons depletes O₂ in sediments and triggers bacterial sulfate reduction to produce the H₂S required by the mats. Sediment samples from GC 185 (Bush Hill) contain high concentrations of oil (mean = 24,775 ppm) and C₁–C₅ hydrocarbons (mean = 11,037 ppm) that are altered by bacterial oxidation. Tube worm communities requiring H₂S occur at GC 185 where the sea floor has been greatly modified since the Pleistocene by accumulation of oil, thermogenic gas hydrates, and authigenic carbonate rock. Venting to the water column is suppressed by this sea-floor modification, enhancing bacterial activity in sediments. Sediments from an area with vesicomyid clams (GC 272) contain lower concentrations of oil altered by bacterial oxidation (mean = 1716 ppm) but C₁–C₅ concentrations are high (mean = 28,766 ppm). In contrast to other sampling areas, a sediment associated with the methanotrophic Seep Mytilid I (GC 233) is characterized by low concentration of oil (82 ppm) but biogenic methane (C₁) is present (8829 ppm).     

Hydrocarbon traces in the Tertiary basalts of the Faeroe Islands

Hydrocarbons in the form of gases, oils and waxes have been observed in the basalts of the Faeroe Islands in the North Atlantic. Gases and traces of oil were observed in the outflowing water of the deep Lopra-1 well drilled in 1981. The hydrocarbon gas was fairly dry, with stable isotopic ratios of δ¹³C₁₋₃=−41.4; −32.4; −26.5% respectively, typical of a thermogenic gas. High temperature gas chromatography of the oil showed that it consisted mostly of C₁₃₋₆₀ n-alkanes. Biomarker distribution observed by GC-MS indicates that the oil was derived from a mature source rock deposited in an anoxic environment; this suggests that the source rock must lie beneath the known basalts.Waxes exhibiting bright yellow fluorescence under UV light were observed as coatings on zeolite minerals widely distributed on the Faeroe Islands. The waxes consist predominantly of higher n-alkanes shown by HTGC. The fluorescence indicates the presence of aromatic compounds. Biomarker distribution indicated that the waxes were derived at least in part from a source rock containing some terrestrial organic matter astestified by the low amounts of oleanane present. The waxes were probably deposited from traces of oil present in deeply circulating waters in fractures within the basalts.Coals which had been suspected to generate some of the hydrocarbons observed in the Faeroese basalts were also examined. Vitrinite values of R_o=0.5% as well as GC-MS analyses of the Suduroy coal extracts showed that these coals are immature and have not generated significant hydrocarbons.     

Origin of crude oils from oilfields in the Zagros Fold Belt,southern Iraq: Relation to organic matter input and paleoenvironmental conditions

Crude oil samples from Cretaceous and Tertiary reservoir sections in the Zagros Fold Belt oil fields, southern Iraq were investigated using non-biomarker and biomarker parameters. The results of this study have been used to assess source of organic matter, and the genetic link between oils and their potential source rocks in the basin. The oils are characterized by high sulphur and trace metal (Ni, V) contents and relatively low API gravity values (17.4–22.7° API). This indicates that these oils are heavy and generated from a marine source rock containing Type II-S kerogen. This is supported by their biomarker distributions of normal alkanes, regular isoprenoids, terpanes and steranes and the bulk carbon isotope compositions of their saturated and aromatic hydrocarbons. The oils are characterized by low Pr/Ph ratios (<1), high values of the C₃₅ homohopane index and C₃₁-22R/C₃₀ hopane ratios, relatively high C₂₇ sterane concentrations, and the predominance of C₂₉-norhopane. These biomarkers suggest that the oils were generated predominantly from a marine carbonate source rock, deposited under reducing conditions and containing plankton/algal and microorganisms source input. The presence of gammacerane also suggests water column stratification during source rock deposition.The biomarker characteristics of the oils are consistent with those of the Middle Jurassic Sargelu carbonate as the effective source rock in the basin. Biomarker maturity data indicate that the oils were generated from early maturity source rocks.     

多环芳烃油指纹应用于船舶溢油鉴别研究

溢油种类主要包括船舶燃料油和原油,二者性质的差异决定了鉴别方法也相应不同,寻求适合于船舶溢油的鉴别方法具有重要意义。在使用柱色谱层析方法对样品进行分离前处理的基础上,以气相色谱/质谱方法(GC-MS)为主要分析手段,对溢油样品和可疑船舶溢油源样品的多环芳烃油指纹特征进行对比,并在多环芳烃油指纹参数的基础上进一步进行多环芳烃内组成三角图分布特征与聚类分析研究,成功为珠江口水域某船舶溢油事故追踪到肇事溢油源。结果表明:取自丁船的油样和现场溢油样芳烃油指纹特征最为相近,是此次溢油事故的溢油源。受风化作用后的船舶燃料油中饱和烃类化合物数量稀少,且含量极低,不适合用于溢油鉴别,而多环芳烃类化合物较饱和烃类化合物而言具有含量高、种类丰富的特点,是该类溢油鉴别的主要油指纹依据。使用油指纹参数进行可疑溢油源识别时,充分考虑油品中有机分子所受风化影响程度的不同是风化条件下溢油鉴定的关键。因此,多环芳烃油指纹可以有效应用于船舶燃料油溢油的鉴别。     

In situ sampling reveals rapid uptake and depuration of polycyclic aromatic hydrocarbons by surf clams (Paphies subtriangulata) affected by the Rena oil spill

ABSTRACT

To investigate the uptake and depuration of polycyclic aromatic hydrocarbons associated with the Rena oil spill we sampled the surf clam Paphies subtriangulata at two open coast locations (6?km apart) just prior to oil coming ashore (7 October 2011), then at 1–3 week intervals for the next 4 months. Total polycyclic aromatic hydrocarbons (tPAH) increased at both sites from 1 to 96–124?µg?kg^?1 (wet weight) by 18 October before declining to low levels (<4?µg?kg^?1) by February 2012. Ongoing sampling throughout 2012–2014 included three additional sites to the north east (up to 30?km away) and a site 5?km to the south east revealing tPAH levels generally <10?µg?kg^?1 except in October 2013 where levels ranged between 39–45?µg?kg^?1 at all sites. A comparison of PAH component profiles with oil-contaminated beach sediment indicated that the high levels observed in surf clams between October–December 2011 were clearly associated with the Rena spill. However, the October 2013 peak had a PAH profile inconsistent with weathered Rena oil, suggesting an alternative source of contamination. Our results highlight the potential for P. subtriangulata as a PAH monitoring tool but recognise more study is needed to better quantify baseline levels and uptake and depuration dynamics.     

In situ microbial degradation of Prudhoe Bay crude oil in Beaufort Sea sediments

This study examined the fate of Prudhoe Bay crude oil in nearshore sediments of the Beaufort Sea, in situ, with emphasis on the rôle of microorganisms in the weathering process. The results indicate that oil is degraded in Arctic sediments very slowly; only after 1 year's exposure was biodegradation evident. Several factors probably contributed to the slow rate of microbial weathering, including: limited populations of hydrocarbon utilising microorganisms; localised high oil concentrations; low temperatures; limiting nutrient concentrations (unfavourable C:N and C:P ratios); low oxygen tensions and limited circulation of interstitial waters in fine-grained sediments. Abiotic weathering of the oil was also slow, with limited loss of low molecular weight aliphatic and aromatic hydrocarbons during 2 years' exposure. Significant features of the overall weathering process were: lack of initial loss of low molecular weight compounds; aliphatic compounds were not preferentially degraded over aromatic compounds and C₁₇, and lower molecular weight normal alkanes were preferentially degraded over higher molecular weight alkanes. The results of this study indicate that hydrocarbons will persist relatively unaltered for several years if Beaufort Sea sediments are contaminated with petroleum.     

Characterization of hydrocarbons in a subsurface oil-rich layer in the Sargasso Sea

The hydrocarbon composition of seawater samples collected within a subsurface oil-rich layer in the southwest North Atlantic Ocean (Sargasso Sea) during February–March, 1978, has been examined in detail. Chromatograms generated through gas chromatographs/mass spectrometry (GC/MS) analyses of saturated and aromatic hydrocarbons are characterized by a narrow unresolved envelope (UCM or unresolved complex mixture) containing isoprenoids as major resolved peaks, suggesting a petroleum source which has undergone moderate biodegradative weathering. Distributions of terpanes, steranes and polycyclic aromatic hydrocarbons corroborate the inferred fossil origin. Stable carbon isotopic compositions (δ¹³C) suggest that the source of these hydrocarbons is enriched in ¹³C in comparison with most petroleums. The results support the previous suggestions (Harvey et al., 1979) that this layer is part of a massive submarine oil seep originating somewhere on the Venezuelan shelf, although its origin cannot be attributed to seepage of a specific oil formation.     

Normal paraffin profiles of pelagic tar samples from the marmap survey

Pelagic tar samples from twenty stations on cruises of the research vessels ALBATROSS IV (72-6) and DELAWARE II (72-19) were analyzed by gas chromatography to obtain semi-quantitative profiles of normal paraffins in the range from C₁₀ to C₃₅ and a qualitative indication of the relative amount of other compounds having a volatility in that same range. These samples are essentially all weathered residues of waxy paraffinic crude oils, and are similar (with respect to the parameters measured) to numerous samples collected in the Sargasso Sea near Bermuda.     

Peculiarities in the distribution of hydrocarbons in the southeastern part of the Baltic Sea

Data on the contents and compositions of the hydrocarbons (HCs)—aliphatic (AHCs) and polycyclic aromatic (PAHs)—are provided in comparison with the contents of the total organic carbon (C_org), the lipids in the particulates, and the C_org in bottom sediments. Particular attention has been paid to the distribution of the HCs in the water area of the Kravtsov oil field. It has been established that the concentrations of AHCs in the water are governed by the content of particulates, and the elevated AHC concentrations are confined to the coastal areas. In the water area of platform D-6, the sandy bottom sediments were notable for the great variability of the HC concentrations, both laterally and from year to year. In the summer of 2010, the content of AHCs averaged 40 μg/g (19% in the C_org), and that of PAHs, 23 ng/g. Natural seepage from the sediment mass is considered to be a source of HCs along with oil contamination.     

综合风化条件下渤海原油中PAHs 变化特征研究

以渤海某原油作为研究对象进行50 d综合模拟风化实验,探讨了原油中五类PAHs组分的分布情况及其风化规律.结果表明:经过50 d风化,原油中PAHs的分布发生了较大的改变:萘系列化合物损失最为严重,相对浓度的损失达到56.78%;菲系列所占的比例有所提高,二苯并噻吩、屈、芴系列则保持相对稳定,其分布特征变化规律为进一步筛选溢油来源鉴别新诊断比值参数提供了一定的导向性;经风化检验,现有常用6种PAHs诊断比值在风化50 d后稳定性良好,可用于风化溢油的鉴别.     

Hydrocarbons in the Bay of Bengal and Central Indian Basin bottom sediments: indicators of geochemical processes in the lithosphere

A study on the bulk distributions and molecular structures of n-alkanes and polycyclic aromatic hydrocarbons (PAH) in organic matter of the sediments from the Bay of Bengal and the Eastern and Central Indian Basins was undertaken. The former two regions represent areas characterised by “normal” sedimentation while the third one mainly represents a region of “active tectonism”. Content of the hydrocarbons in the sediments of “normal” sedimentation ranges between 4.6 and 10.5 μg/g and aromatic hydrocarbons ranges between 0 and 0.38 μg/g. n-Alkanes in the sediments of the northern deep part of the Bay of Bengal consist mostly of long-chain structures (total C₂₅–C₃₃ up to 70%) with a high carbon preference index (CPI=3.01–3.43), indicating a large contribution of organic matter from terrigenous sources. The sediments from the Eastern Indian Basin have n-alkane distributions in which the long-chain components did not exceed 52.5% and the CPI was 1.7–1.90, indicating that the hydrocarbons are mostly derived from marine sources. Sharp increases of hydrocarbons are found in the vicinity of the tectonically active region of the Central Indian Basin, particularly in the sediments collected from the fracture zone. The total concentration of hydrocarbons increase to 170 μg/g and the aromatic hydrocarbons fraction to 156.3 μg/g. The proportion of short-chain n-alkanes increases up to 70%, CPI decreases to 0.76–1.12, and high concentrations of n-C₁₆ (16–40%) occur, all of which are absent in the other samples. The molecular content of PAH includes the unsubstituted individual structures: biphenyl, fluorene, pyrene, perylene, benzo(ghi)perylene, and the groups of homologues of naphthalene, benzofluorene, phenanthrene and chrysene. The association of the PAH and composition of paraffin hydrocarbons in the surficial sediments of deformation zone indicate that these are the resultant products of hydrothermal processes. It is, therefore, suggested that the association and composition of the hydrocarbons in sediments can be utilised as a paleoceanographic parameter to decipher the history of tectonism of an area.     

Triterpenoids as molecular indicators of paleoseepage in recent sediments of the Southern California bight

Petroleum-derived hydrocarbons have been identified in sediments by analysis of the n-alkanes, aromatic hydrocarbons and branched and cyclic components (humps). The detection of low levels of petroleum input to sediments can be ambiguous due to the presence of syngenetic biolipids. Triterpenoids, especially the (17αH, 21βH)-hopanes, have been proposed as sensitive molecular markers of petroleum pollution.Recent sediments from the Southern California Bight to subbottom depths of about 30 cm (pre-anthropogenic) contain lipids of syngenetic origin with major humps of branched and cyclic material and triterpenoids consisting mainly of the (17αH, 21βH)-hopanes ranging from C₂₇ to C₃₅. Extended hopanes (> C₃₁) are found as 1:1 mixtures of the 22R and 22S diastereomers. The 17α(H),18α(H), 21β(H)-28,30-bisnorhopane is the dominant triterpane for most of these sediments and appears to be a potential molecular marker characteristic of the Southern California petroleums. Extended tricyclic diterpanes ranging from C₁₉ to C₂₇ are also present and their structures make them further possible indicators of petroleum. Southern California Bight sediments therefore appear to contain petroleum products from both seepage and anthropogenic activity.Recent sediments from other areas (e.g. Guaymas Basin, Gulf of California; Cook Inlet, Alaska; Eastern Bering Sea; Walvis Bay, Southwest Africa; and Mangrove Lake, Bermuda) contain predominantly (17βH, 21βH)-hopanes and hopenes, indicating recent synthesis and no petroleum pollution.     

The petroleum geochemistry of the Termit Basin,Eastern Niger

Sixty crude oils from the Termit Basin (Eastern Niger) were analysed using biomarker distributions and bulk stable carbon isotopic compositions. Comprehensive oil-to-oil correlation indicates that there are two distinct families in the Termit Basin. The majority of the oils are geochemically similar and characterized by low Pr/Ph (pristane to phytane ratios) and high gammacerane/C₃₀ hopane ratios, small amounts of C₂₄ tetracyclic terpanes but abundant C₂₃ tricyclic terpane, and lower δ¹³C values for saturated and aromatic hydrocarbon fractions. All of these geochemical characteristics indicate possible marine sources with saline and reducing depositional environments. In contrast, oils from well DD-1 have different geochemical features. They are characterized by relatively higher Pr/Ph and lower gammacerane/C₃₀ hopane ratios, higher amounts of C₂₄ tetracyclic terpane but a low content of C₂₃ tricyclic terpane, and relatively higher δ¹³C values for saturated and aromatic hydrocarbon fractions. These geochemical signatures indicate possible lacustrine sources deposited under freshwater, suboxic-oxic conditions. This oil family also has a unique biomarker signature in that there are large amounts of C₃₀ 4α-methylsteranes indicating a freshwater lacustrine depositional environment.The maturity of the Termit oils is assessed using a number of maturity indicators based on biomarkers, alkyl naphthalenes, alkyl phenanthrenes and alkyl dibenzothiophenes. All parameters indicate that all of the oils are generated by source rocks within the main phase of the oil generation stage with equivalent vitrinite reflectance of 0.58%–0.87%.     

Molecular and isotopic compositions of bitumens in Silurian tar sands from the Tarim Basin,NW China: Characterizing biodegradation and hydrocarbon charging in an old composite basin

Biodegradation and oil mixing in Silurian sandstone reservoirs of the Tarim Basin, one of the largest composite basins in China, were investigated by analyzing the molecular characteristics and stable carbon isotopic signatures of low-molecular-weight (LMW) saturated hydrocarbons and high-molecular-weight (HMW) asphaltenes. Detection of 25-norhopanes and 17-nortricyclic terpanes in most Silurian tar sands from the Tabei Uplift in the Tarim Basin suggests a much greater degree of biodegradation here than in the Tazhong Uplift. This explains the relatively more abundant tricyclic terpanes, gammacerane, pregnane and diasteranes in tar sands from the Tabei Uplift than in those from the Tazhong Uplift. Hence, care must be taken when assigning oil source correlations using biomarkers in tar sands because of the biodegradation and mixing of oils derived from multiple sources in such an old composite basin. Asphaltenes in the tar sands seem to be part of the oil charge before biodegradation, depending on the relative anti-biodegradation characteristics of asphaltenes, the similarity in carbon isotopic signatures for asphaltenes and their pyrolysates, and the consistent product distribution for flash pyrolysis and for regular steranes in asphaltene pyrolysates, regardless of whether the tar sands were charged with fresh oil. According to the relative distributions of regular steranes and the relatively abundant 1,2,3,4-tetramethylbenzene significantly enriched in ¹³C, the oil sources for asphaltenes in the tar sands might be related to lower Paleozoic marine source rocks formed in euxinic conditions. Nevertheless, the relatively low abundance of gammacerane and C₂₈ regular steranes observed in asphaltene pyrolysates and residual hydrocarbons, within limited samples investigated in this work, made a direct correlation of oils originally charged into Silurian tar sands with those Cambrian source rocks, reported so far, seem not to be possible. Comparison of carbon isotopic signatures of n-alkanes in asphaltene pyrolysates with those of LMW saturated hydrocarbons is helpful in determining if the abundant n-alkanes in tar sands are derived from fresh oil charges after biodegradation. The limited carbon isotopic data for n-alkanes in LMW saturated hydrocarbons from the tar sands can be used to classify oils charged after biodegradation in the composite basin into four distinct groups.     

Evolution des hydrocarbures,des peuplements bacteriens et microphytiques dans les sediments des marais maritimes de l'iie grande pollues par l'amoco cadiz: 1, evolution des hydrocarbures et des bacteries

The evolution of hydrocarbons in sediments was studied from 1978 to 1980 at eight stations in the Ile Grande marshes (Brittany) polluted by the Amoco Cadiz oil spill. Generally, in 1980 (except for one heavily polluted site) the amounts of hydrocarbons were found to be far less important than in 1978 and sometimes biogenic hydrocarbons were found. In the superficial layer of the sediments biodegradation processes were generally important with the preferential degradation of n-alkanes. On the other hand, aromatic hydrocarbons seem not to have been altered after three years. Degradation of percolated hydrocarbons proceeds more slowly than in the surface layer. The number of degrading bacteria decreases when n-alkanes disappear.