Relationship between hydrocarbons and bacterial activity in mediterranean sediments: Part 2—hydrocarbon degrading activity of bacteria from sediments

In marine sediments from the Mediterranean coast polluted by oil spills (Etang de Berre) high bacterial activity is responsible for self-purification, samples collected from these areas showing a bacterial density several orders of magnitude higher than samples from non-polluted areas (Isle des Embiez). Between 60 and 80 % of the heterotrophic bacteria in the polluted areas are hydrocarbon-degrading, compared with 0.01 % in the non-polluted area.Several strains of hydrocarbon utilisers were isolated, a mixture of strains from each biotope was taken to represent a ‘biotope population’ and their activity towards different types of hydrocarbons (n-alkanes, iso-alkanes, cycloalkanes, aromatics) was determined.With ammonia as the nitrogen source the ‘biotope population’ from the polluted area degraded hydrocarbons much more readily than the ‘biotope population’ from the non-polluted area. With nitrate as the nitrogen source the degradation was much reduced, and, for some hydrocarbons, ceased in both ‘populations’.Individual hydrocarbons encouraged the growth of individual strains in the ‘biotope population’. In natural mixtures of hydrocarbons all strains grew well and degraded aliphatics. There was a good correlation between the respiratory activity of the ‘biotope population’ and the ability of the ‘population’ to utilise hydrocarbons for growth.     

A comparison of sedimentary aliphatic hydrocarbon distribution between the southern Okinawa Trough and a nearby river with high sediment discharge

Twelve surface sediments from the southern Okinawa Trough (OT) and nine surface sediments from a nearby river, the Lanyang River (LR), with high sediment discharge were analyzed for comparison of their aliphatic hydrocarbon distributions. Performing cluster analysis on all hydrocarbon data of LR and OT sediments showed that the two areas had a similarity level of only 0.15, meaning that they were quite dissimilar. The average ratio of terrigenous to aquatic n-alkanes was 0.99 for LR sediments and 9.64 for OT sediments, indicating that the concentrations of n-alkanes in LR and OT sediments were quite different. Furthermore, the mean pristane/phytane ratios for LR and OT sediments were 1.01 and 2.57, respectively; the difference between them was significant (Student's t test, at the 99% significance level). The carbon preference index (CPI) of C₂₅–C₃₃ n-alkanes averaged 3.26 (range 2.16–4.59) for LR sediments and 2.92 (range 2.35–5.24) for OT sediments; no significant difference was found between the two CPI averages (Student's t test, at the 99% confidence level). However, higher plant n-alkanes generally maximized at C₂₉ for LR sediments, but maximized at C₃₁ for all OT sediments, strongly indicating significant differences in the origins of the hydrocarbons in these two areas. All present results appear to suggest that LR sediments are not a major hydrocarbon source for OT sediments. In addition, there was no positive, linear correlation between diploptene (hop-22(29)-ene) and terrestrial higher plant n-alkanes for LR and OT sediments.     

Higher plant n-alkane average chain length as an indicator of petrogenic hydrocarbon contamination in marine sediments

The n-alkane average chain length (ACL) is the weight-averaged number of carbon atoms of the higher plant C₂₅–C₃₃ n-alkanes. The abundance of individual n-alkanes from higher plant sources generally increases with increasing carbon number in coastal marine sediments around Taiwan, but this trend is reversed for petrogenic hydrocarbons. The ACL would potentially be lowered if petrogenic hydrocarbons were added to sediments containing biogenic hydrocarbons alone. To test this idea, a marine environment off southwestern Taiwan known to contain both biogenic and petrogenic hydrocarbons and two nearby rivers were selected for investigating possible difference in ACL values between their sediments. The average CPI of C₂₅–C₃₃ n-alkanes was 4.08 ± 2.04 (range 1.90–8.96, n = 15) for the river sediments and 1.70 ± 0.16 (range 1.43–1.97, n = 15) for the marine sediments. The ACL of C₂₅–C₃₃ n-alkanes for river sediments ranged from 29.2 to 30.5 (average 29.9 ± 0.4), and for marine sediments from 28.4 to 29.3 (average 28.9 ± 0.3). The ACL difference between marine and river sediments was significant (Student's t test at 99% confidence) although it appeared small. It is suggested that the ACL can be an additional indicator for detection of petrogenic hydrocarbons in coastal marine sediments.     

Evolution des hydrocarbures et des populations bactériennes et microphytiques dans les sédiments des marais maritimes de l'ile grande pollués par l'Amoco cadiz: 2—Evolution des peuplements microphytiques

In this work we attempt to estimate the short- and long-term effects of the Amoco Cadiz oil spill on benthic microalgal populations (cyanophytes and diatoms) which, under natural conditions, live on upper layers of ‘schorres’ soils or of ‘slikke’ muds in the Ile Grande salt marsh system (Côtes du Nord, France). These populations were completely destroyed in 1978 in the oil-affected sites. Ubiquitous species settled fairly rapidly on intertidal polluted muds (tidal flat). The chlorophyll a content values reached 100 μg g⁻¹ dry sediment, i.e. 1000 mg m⁻² in 1980. Conversely, the salt marsh soils are still much less densely repopulated 3 years after the Amoco Cadiz grounding—especially when they are infrequently flooded (3 to 40 μg Chl.a g⁻¹, i.e. 40 to 270 mg m⁻²). Some of these soils remain ten times less populated than reference stations.     

Petroleum pollution in surface sediments of Daya Bay,South China,revealed by chemical fingerprinting of aliphatic and alicyclic hydrocarbons

Nine surface sediments collected from Daya Bay have been Soxhlet-extracted with 2:1 (v/v) dichloromethane-methanol. The non-aromatic hydrocarbon (NAH) fraction of solvent extractable organic matter (EOM) and some bulk geochemical parameters have been analyzed to determine petroleum pollution of the bay. The NAH content varies from 32 to 276 μg g⁻¹ (average 104 μg g⁻¹) dry sediment and accounts for 5.8–64.1% (average 41.6%) of the EOM. n-Alkanes with carbon number ranging from 15 to 35 are identified to be derived from both biogenic and petrogenic sources in varying proportions. The contribution of marine authigenic input to the sedimentary n-alkanes is lower than the allochthonous input based on the average n-C₃₁/n-C₁₉ alkane ratio. 25.6–46.5% of the n-alkanes, with a mean of 35.6%, are contributed by vascular plant wax. Results of unresolved complex mixture, isoprenoid hydrocarbons, hopanes and steranes also suggest possible petroleum contamination. There is strong evidence of a common petroleum contamination source in the bay.     

Contrasting chemical and isotopic compositions of organic matter in Changjiang (Yangtze River) estuarine and East China Sea shelf sediments

To examine the source and preservation of organic matter in the shelf sediments of the East China Sea (ECS), we measured bulk C/N and isotopes, organic biomarkers (n-alkanes and fatty acids) and compound-specific (fatty acids) stable carbon isotope ratios in three sediment cores collected from two sites near the Changjiang Estuary and one in the ECS shelf. Contrasting chemical and isotopic compositions of organic matter were observed between the estuarine and shelf sediments. The concentrations of total n-alkanes and fatty acids in the shelf surface sediments (0–2 cm) were 5–10 times higher than those in estuarine surface sediments but they all decreased rapidly to comparable levels below the surface layer. The compositions of n-alkanes in the estuarine sediments were dominated by C₂₆-C₃₃ long-chain n-alkanes with a strong odd-to-even carbon number predominance. In contrast, the composition of n-alkanes in the shelf sediment was dominated by nC₁₅ to nC₂₂ compounds. Long-chain (>C₂₀) fatty acids (terrestrial biomarkers) accounted for a significantly higher fraction in the estuarine sediments compared to that in the shelf sediment, while short-chain (<C₂₀) saturated and unsaturated fatty acids were more abundant in the shelf surface sediments than in the estuarine sediments. Stable carbon isotopic ratios of individual fatty acids showed a general positive shift from estuarine to shelf sediments, consistent with the variations in bulk δ ¹³C_TOCTOC. These contrasts between the estuarine and shelf sediments indicate that terrestrial organic matter was mainly deposited within the Changjiang Estuary and inner shelf of ECS. Post-depositional diagenetic processes in the surface sediments rapidly altered the chemical compositions and control the preservation of organic matter in the region.     

Fluxes,source and transport of organic matter in the western Sea of Okhotsk: Stable carbon isotopic ratios of n-alkanes and total organic carbon

Settling particles and surface sediments collected from the western region of the Sea of Okhotsk were analyzed for total organic carbon (TOC), long-chain n-alkanes and their stable carbon isotope ratio (δ¹³C) to investigate sources and transport of total and terrestrial organic matter in the western region of the sea. The δ¹³C measurements of TOC in time-series sediment traps indicate lateral transport of resuspended organic matter from the northwestern continental shelf to the area off Sakhalin via the dense shelf water (DSW) flow at intermediate depth. The n-alkanes in the surface sediments showed strong odd carbon number predominance with relatively lighter δ¹³C values (from −33‰ to −30‰). They fall within the typical values of C3-angiosperms, which is the main vegetation in east Russia, including the Amur River basin. On the other hand, the molecular distributions and δ¹³C values of n-alkanes in the settling particles clearly showed two different sources: terrestrial plant and petroleum in the Sea of Okhotsk. We reconstructed seasonal change in the fluxes of terrestrial n-alkanes in settling particles using the mixing model proposed by Lichtfouse and Eglinton [1995. ¹³C and ¹⁴C evidence of a soil by fossil fuel and reconstruction of the composition of the pollutant. Organic Geochemistry 23, 969–973]. Results of the terrestrial n-alkane fluxes indicate that there are two transport pathways of terrestrial plant n-alkanes to sediments off Sakhalin, the Sea of Okhotsk. One is lateral transport of resuspended particles with lithogenic material from the northwestern continental shelf by the DSW flow. Another is the vertical transport of terrestrial plant n-alkanes, which is independent of transport of lithogenic material. The latter may include dry/wet deposition of aerosol particles derived from terrestrial higher plants possibly associated with forest fires in Siberia.     

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.     

Sources and transport of organic carbon to shelf,slope, and basin surface sediments of the Arctic Ocean

Lipids in surface sediment transects across the Arctic Ocean were identified to define the sources of organic carbon and the transport of material in the ocean basin. Sterols representing diatoms (24-methylcholesta-5,24(28)-dien-3β-ol, 24-methylcholesta-5,22-dien-3β-ol) and dinoflagellates (4α,23,24-trimethylcholest-22-en-3β-ol) together with algal polyunsaturated fatty acids (20:5, 22:6) demonstrated the importance of primary production to organic matter inputs on the Chukchi Shelf. The presence of terrestrial biomarkers including long-chain n-alkanes and mono- and dicarboxylic acids in shelf sediments indicated that while the fraction of terrestrial biomarkers was small compared to marine material, the transport of allochthonous material impacts carbon cycling on the shelf. Algal biomarkers were found in all surficial sediments from the central Arctic basins, demonstrating that some fraction of primary production reached bottom sediments despite ice cover and light limitation. Marine markers represented a small fraction of the total lipids in central basin sediments. This implies that the basins are less productive than shallow waters, significant degradation occurs before the organic matter reaches the sediment–water interface, and substantial amounts of vascular plant material are exported to the central Arctic. Circulation and topographical features, such as the Transpolar Drift and the Lomonosov Ridge, appear to have an important influence on the transport and focusing of terrestrial material in the Arctic Ocean basins.     

Composition research of <Emphasis Type="Italic">n</Emphasis>-alkanes in the samples of hydrothermal deposits of the Mid-Atlantic Ridge by means of gas chromatography-mass spectrometry

The optimum conditions were selected for the chromatographic separation of model mixtures of C₁₂–C₄₀ n-alkanes. For one of the samples of hydrothermal deposits, the extraction conditions of the hydrocarbons were studied and a sample preparation procedure was selected. A procedure is proposed to determine the n-alkanes in samples of hydrothermal deposits by means of gas chromatography-mass spectrometry (GC-MS). The detection limit for the n-alkanes amounted to 3 × 10⁻⁹ to 10⁻⁸% depending on the components. On the basis of the procedure proposed, the composition of the n-alkanes was studied in the samples of hydrothermal deposits collected at the Mid-Atlantic Ridge (the Broken Spur, Lost City, and Rainbow fields). The analysis performed showed that the samples treated contained C₁₄-C₃₅ n-alkanes. The concentrations of the n-alkanes considered were rather low and varied from 0.002 to 0.038 μg/g. Hypotheses concerning the genesis of the n-alkanes identified were formed.     

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.     

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.     

Evolution des hydrocarbures dans des sédiments côtiers méditerranéens prélevés à proximité d'un emissaire d'une raffinerie de pétrole

Coastal Mediterranean sediments highly polluted by refinery effluents have been studied for their hydrocarbon content and bacterial activity. The study has taken into account both the distance from the refinery and depth of sampling. Very high hydrocarbon concentrations have been found (1–250 g/kg dry sediment). Micro-organisms in the sediments have a high bacterial activity and a good correlation exists between hydrocarbon concentrations and bacteria able to use these substrates as a carbon and energy source.     

Sources and preservation of organic matter in Plum Island salt marsh sediments (MA, USA): long-chain n-alkanes and stable carbon isotope compositions

Elemental (TOC, TN, C/N) and stable carbon isotopic (δ¹³C) compositions and n-alkane (nC_16–38) concentrations were measured for Spartina alterniflora, a C₄ marsh grass, Typha latifolia, a C₃ marsh grass, and three sediment cores collected from middle and upper estuarine sites from the Plum Island salt marshes. Our results indicated that the organic matter preserved in the sediments was highly affected by the marsh plants that dominated the sampling sites. δ¹³C values of organic matter preserved in the upper fresh water site sediment were more negative (−23.0±0.3‰) as affected by the C₃ plants than the values of organic matter preserved in the sediments of middle (−18.9±0.8‰) and mud flat sites (−19.4±0.1‰) as influenced mainly by the C₄ marsh plants. The distribution of n-alkanes measured in all sediments showed similar patterns as those determined in the marsh grasses S. alterniflora and T. latifolia, and nC₂₁ to nC₃₃ long-chain n-alkanes were the major compounds determined in all sediment samples. The strong odd-to-even carbon numbered n-alkane predominance was found in all three sediments and nC₂₉ was the most abundant homologue in all samples measured. Both δ¹³C compositions of organic matter and n-alkane distributions in these sediments indicate that the marsh plants could contribute significant amount of organic matter preserved in Plum Island salt marsh sediments. This suggests that salt marshes play an important role in the cycling of nutrients and organic carbon in the estuary and adjacent coastal waters.     

Incorporation,distribution and fate of saturated petroleum hydrocarbons in sediments from a controlled marine ecosystem

A simulation of a chronic input of petroleum into an estuarine environment was investigated using the facilities at the Marine Ecosystems Research Laboratory at the University of Rhode Island. An oil-water dispersion of No. 2 fuel oil was added to the system (twice weekly for 24 weeks) and the saturated hydrocarbons from this oil were measured in suspended material and sediments. After the initial chronic oil addition, trace amounts of hydrocarbons were detected in the sediments within two weeks, but substantial accumulation was not detected for approximately 135 days. The oil appeared to enter the sediment via the suspended material, with most of the saturated hydrocarbons associated with smaller size sediment particles (< 45 μm to > 0·3 μm). With time, the fuel oil saturated hydrocarbons in the sediments were mixed to a depth of 3 to 4 cm. Although only 12% of the total saturated hydrocarbons added to the system were found in the sediments, these hydrocarbons appear to be relatively stable and were still detectable in these sediments for at least six months after the last oil addition.     

Comparison of bulk and compound-specific δC analyses and determination of carbon sources to salt marsh sediments using n-alkane distributions (Maine,USA)

Sources of sedimentary organic matter to a Morse River, Maine (USA) salt marsh over the last 3390 ± 60 RCYBP (Radiocarbon Years Before Present) are determined using distribution patterns of n-alkanes, bulk carbon isotopic analysis, and compound-specific carbon isotopic analysis. Marsh foraminiferal counts suggest a ubiquitous presence of high marsh and higher-high marsh deposits (dominated by Trochammina macrescens forma macrescens, Trochammina comprimata, and Trochammina inflata), implying deposition from ∼0.2 m to 0.5 m above mean high water. Distributions of n-alkanes show a primary contribution from higher plants, confirmed by an average chain length value of 27.5 for the core sediments, and carbon preference index values all >3. Many sample depths are dominated by the C₂₅ alkane. Salicornia depressa and Ruppia maritima have similar n-alkane distributions to many of the salt marsh sediments, and we suggest that one or both of these plants is either an important source to the biomass of the marsh through time, or that another unidentified higher plant source is contributing heavily to the sediment pool. Bacterial degradation or algal inputs to the marsh sediments appear to be minor. Compound-specific carbon isotopic analyses of the C₂₇ alkane are on average 7.2‰ depleted relative to bulk values, but the two records are strongly correlated (R² = 0.89), suggesting that marsh plants dominate the bulk carbon isotopic signal. Our study underscores the importance of using caution when applying mixing models of plant species to salt marsh sediments, especially when relatively few plants are included in the model.     

北黄海泥质区多环芳烃与黑碳的沉积记录

在北黄海中部泥质区采集柱状沉积物样品,对多环芳烃(PAHs)和黑碳(BC)的含量和来源进行研究。结果表明:(1)PAHs的含量变化范围为207~611ng/g;BC的含量变化范围为0.560~1.32mg/g;(2)对比低分子量(LMW)和高分子量(HMW)PAHs含量的历史变化趋势,发现1980s之前的PAHs主要来自于生物质的低温燃烧,之后主要来自于化石燃料的高温热解;(3)1920s之前,PAHs与BC含量基本保持稳定且处于较低值。1920s-1980s,PAHs含量受工业化和煤炭发展的影响较大,开始出现增长趋势。1980-1990s,由于能源消耗量的大幅度增加,导致PAHs和BC的含量迅速升高并达到最大值(1996年)。1990s初期-2000s初期,由于清洁能源的使用等原因,PAHs与BC含量都开始下降。(4)对PAHs和BC含量进行Spearman相关性分析,得出在1920年之前和1920-1980年之间,BC和PAHs含量无显著性相关(r=-0.25,P0.05,n=34;r=0.06,P0.06,n=11);而1980年之后,BC和PAHs含量呈显著性相关(r=0.90,P=0.04,n=5)。     

Hydrocarbons in Washington coastal sediments

The sources and distributions of polycyclic aromatic hydrocarbons (PAH) and aliphatic hydrocarbons are characterized in seventeen sediments from a highly river-influenced sedimentary environment off the southwestern coast of Washington. The major hydrocarbons are land-derived, introduced as preformed compounds and display long-term stability in sediment cores. A series of PAH of anthropogenic origin and two naturally derived compounds, retene and perylene, dominate the PAH composition in these sediments. Plantwax n-alkanes are the major aliphatic hydrocarbon constituents. Aliphatic hydrocarbons of marine origin, pristane and a series of four acyclic, multibranched C₂₅ polyolefins, are also observed in many sediments. The concentrations of these marine-derived hydrocarbons decrease to negligible levels rapidly with sediment depth from the sea-sediment interface, suggesting degradation.In general, the major land-derived hydrocarbons are concentrated in the midshelf silt deposit which extends northwestward along the continental shelf from the Columbia River mouth. A quantitatively more minor, natural series of phenanthrene homologs, also of terrestrial origin, is preferentially advected further offshore and deposited in continental slope sediments. These distributions are consistent with recognized particle associations for these compounds and sediment dispersal processes in this coastal environment. Sediment core records suggest the present pattern of dispersal has persisted for at least the past century and possibly since the Late Pleistocene.     

The occurrence of hydrocarbons and histopathological abnormalities in oysters for seven years following the wreck of the Amoco Cadiz in Brittany (France)

A study of the main oyster areas polluted by the Amoco Cadiz oil spill (Abers, Baie de Morlaix) was carried out between 1978 and 1985 by chemical analyses (mainly aromatic hydrocarbon determinations) and histopathological observations of lesions in the digestive tracts and gonads of oysters. The hydrocarbon content in oyster tissues was monitored and analyzed by UV spectrofluorimetry, and gas and liquid chromatographic techniques.Seven years after the Amoco Cadiz wreck, the oysters sampled in the AberBenoit and in the Baie de Morlaix (Carantec) are still polluted with residual aromatic hydrocarbons, corresponding, respectively, to about five and two times the values from an unpolluted site (Baie de Saint-Brieuc). Since petroleum residues are buried in anaerobic sediments, especially in the Abers areas, they are expected to persist and accordingly may still contaminate oysters for several more years.Depuration kinetics of contaminated flat and Pacific oysters from the heavily polluted zones (Abers, Carantec) were studied and compared with that of healthy oysters transplanted in the same areas. The decontamination rates of oysters after transfer to a clean environment were heavily dependent on the duration of oil exposure.Necrosis and inflammation were the most significant and noticeable changes occurring during the first months after the pollution. Atrophy of the gonadal cells was detected in the oysters from the Abers only during the first six months of the study. No neoplastic and parasitic diseases have been related to this oil spill.     

Composition of the organic matter of the water,suspended matter,and bottom sediments in Nha Trang Bay in Vietnam in the South China Sea

Research has been conducted in Nha Trang Bay (Southern Vietnam, the South China Sea) at the section from the estuary of the Cai River to the marine part of the bay, as well as in the area of coral reefs. The objects of the studies are the river and sea waters, the suspended matter, and the bottom sediments. Data on the dissolved organic carbon and the total nitrogen in the water are obtained. The organic carbon content is estimated in the suspended matter; the organic carbon and the molecular and group composition of the n-alkanes are determined in the bottom sediments. The molecular and group composition of the n-alkanes in the bottom sediments of the landfill have made it possible to identify three types of organic matter (OM): marine, mixed, and of mainly terrigenous origin. All the types of OM are closely related to the specificity of the sedimentation and the hydrodynamics of the waters in this water area.