Distribution and Origin of Hydrocarbons on a Transarctic Transect

The paper summarizes results on the content and composition of aliphatic hydrocarbons (HCs) in suspended particulate matter (SPM) and bottom sediments in the Kara, Laptev, and East Siberian seas obtained in 2015–2018. It was established that the “losses” in HC concentrations in surface waters in the river (Ob, Yenisei, Lena, Khatanga, Indigirka, Kolyma) and seawater mixing zone in some cases exceeded their river removal by 90%. The composition of HCs in surface waters depends on the characteristics of the river catchment area, sampling season. and time of day (high/low tide) and basically coincides with the SPM distribution. In the pelagic zone of the seas, the HC content is close to the background (2–7 μg/L). The influence of anthropogenic input was established only in the Gulf of Ob, where the composition of alkanes is close to oil with a HC content of 86 μg/mg SPM. In bottom sediments, the particle size distribution determines the HCs, and terrigenous n-alkanes play the dominant role in the molecular composition.

     

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.     

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.     

Marine organic geochemistry of the Eastern Mediterranean: 1. Aliphatic and polyaromatic hydrocarbons in Cretan Sea surficial sediments

As part of a lipid biogeochemical study, aliphatic and polyaromatic hydrocarbons were determined in surficial sediments from the Cretan Sea (South Aegean Sea) in the Eastern Mediterranean. Total concentrations of both aliphatic (AHC) and polyaromatic (PAH) hydrocarbons were low (562–5697 and 14.6–158.5 ng/g, respectively) with respect to other coastal sediments worldwide and compare with concentrations found in open sea areas. The composition of AHC was dominated by unresolved complex mixture (UCM) indicating the presence of petroleum-related hydrocarbon inputs as confirmed by the detection of specific α,β-hopanes. PAH consisted mainly of pyrolytic four- to five-ring compounds. UCM and PAH amounts revealed that Cretan Sea receives low supply of anthropogenic material compared to NW Mediterranean. The spatial distributions of AHC and PAH indicated that urban run-off and transport from the continental self are the major input pathway of anthropogenic and biogenic hydrocarbons from terrestrial sources in the near shore area, whereas atmospheric transport might be the significant source of hydrocarbons in the deep area.     

A refinement of the previous hypothesis of turbulent energy spectrum

To refine the previous hypothesis of turbulent energy spectrum (Nan-niti, 1970), further theoretical consideration and a simple experiment using electric fans was carried out. From the hypothesis ofq=δε/δk andεq=const., the following relations are derived for the spectrumF, and the autocorrelation functionR:F(k)∼k _{−(5−2α)/3} andR(t)∼1−(t/τ)_2(1−α)/3, whereq is the local energy supply,ε the energy dissipation rate, andk the wavenumber,t the time,τ the lifetime of the largest eddy. The following further relations are also obtained:ε∼l _−α,v∼l _β,v∼τ _γ andγ=(1−α)/(2+α)=β/(1−β), wherel is the length scale of the phenomenon,v turbulent velocity,α=1/2,β=1/6, andγ=1/5. The experimental results support these relations.     

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.     

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.     

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.     

Stocks and dynamics of dissolved and particulate organic matter in the southern Ross Sea, Antarctica

Dissolved and particulate organic matter was measured during six cruises to the southern Ross Sea. The cruises were conducted during late austral winter to autumn from 1994 to 1997 and included coverage of various stages of the seasonal phytoplankton bloom. The data from the various years are compiled into a representative seasonal cycle in order to assess general patterns of dissolved organic matter (DOM) and particulate organic matter (POM) dynamics in the southern Ross Sea. Dissolved organic carbon (DOC) and particulate organic carbon (POC) were at background concentrations of approximately 42 and 3 μM C, respectively, during the late winter conditions in October. As the spring phytoplankton bloom progressed, organic matter increased, and by January DOC and POC reached as high as 30 and 107 μM C, respectively, in excess of initial wintertime conditions. Stocks and concentrations of DOC and POC returned to near background values by autumn (April). Approximately 90% of the accumulated organic matter was partitioned into POM, with modest net accumulation of DOM stocks despite large net organic matter production and the dominance of Phaeocystis antarctica. Changes in NO₃ concentration from wintertime values were used to calculate the equivalent biological drawdown of dissolved inorganic carbon (DIC_equiv). The fraction of DIC_equiv drawdown resulting in net DOC production was relatively constant (ca. 11%), despite large temporal and spatial variability in DIC_equiv drawdown. The C : N (molar ratio) of the seasonally produced DOM had a geometric mean of 6.2 and was nitrogen-rich compared to background DOM. The DOM stocks that accumulate in excess of deep refractory background stocks are often referred to as “semi-labile” DOM. The “semi-labile” pool in the Ross Sea turns over on timescales of about 6 months. As a result of the modest net DOM production and its lability, the role DOM plays in export to the deep sea is small in this region.     

In situ tensile fracture toughness of surficial cohesive marine sediments

This study reports the first in situ measurements of tensile fracture toughness, K _IC, of soft, surficial, cohesive marine sediments. A newly developed probe continuously measures the stress required to cause tensile failure in sediments to depths of up to 1 m. Probe measurements are in agreement with standard laboratory methods of K _IC measurements in both potter’s clay and natural sediments. The data comprise in situ depth profiles from three field sites in Nova Scotia, Canada. Measured K _IC at two muddy sites (median grain size of 23–50 μm) range from near zero at the sediment surface to >1,800 Pa m^1/2 at 0.2 m depth. These profiles also appear to identify the bioturbated/mixed depth. K _IC for a sandy site (>90% sand) is an order of magnitude lower than for the muddy sediments, and reflects the lack of cohesion/adhesion. A comparison of K _IC, median grain size, and porosity in muddy sediments indicates that consolidation increases fracture strength, whereas inclusion of sand causes weakening; thus, sand-bearing layers can be easily identified in K _IC profiles. K _IC and vane-measured shear strength correlate strongly, which suggests that the vane measurements should perhaps be interpreted as shear fracture toughness, rather than shear strength. Comparison of in situ probe-measured values with K _IC of soils and gelatin shows that sediments have a K _IC range intermediate between denser compacted soils and softer, elastic gelatin.     

Mineral-forming and diagenetic processes related to Tertiary hydrocarbon seepage at the Bohemian Massif/Outer Western Carpathians interface: Evidence from the Hrabůvka quarry,Moravia, Czech Republic

Ancient hydrocarbon seepage occurred in the Hrabůvka quarry at the boundary between the basement of the Bohemian Massif (represented by folded Lower Carboniferous siliciclastics of the Culm facies) and Tertiary sedimentary cover of the Carpathian Foredeep (formed by Lower Badenian siliciclastics and calcareous clays). The unconsolidated Lower Badenian sediments contain lithified domains composed of limestone and breccias with limestone cement, whereas the basement rocks are cut by subvertical neptunic dykes filled up by limestone and calcite-marcasite-pyrite veinlets representing sealed fluid conduits. The deeply negative δ¹³C values of both vein calcite and limestone (down to −38.1‰ V-PDB) indicate that oxidation of hydrocarbons was the major source of carbon for authigenic mineralization. A fluid inclusion study suggests low fluid temperatures (<50 °C) and low and variable salinities of aqueous fluids associated with hydrocarbons (0.7–6.7 wt. % NaCl eq.). The variability of δ¹⁸O values of authigenic carbonates (−1.7 to −8.2‰ V-PDB) could reflect either slight changes in temperature of escaping fluids (mostly within 15 °C), and/or some mixing with meteoric waters. The low δ³⁴S values of vein marcasite (∼–20‰ V-CDT) are consistent with bacterial reduction of sulfate in the hydrothermal system. Low C₁/(C₂+C₃) ratios in hydrocarbon gas extracted from authigenic carbonates (9.9 and 5.8) as well as the high δ¹³C values of methane (−31.8 and −32.4‰ V-PDB) are compatible with a thermogenic source of hydrocarbons. REE data indicate sequestration of REE from finely dispersed detrital material in the apical part of the hydrothermal system. The available data are compatible with two possible scenarios of fluid origin. The hydrocarbons could have been leached from underlying Paleozoic sedimentary sequence by aqueous fluids that infiltrated into the basement after Tertiary tectonic reactivation. Alternatively, an external source of hydrocarbon-bearing fluids can be found in the adjacent Outer Western Carpathians flysch nappes containing petroleum-producing lithologies. Nevertheless, a regional flow of hydrocarbon-bearing fluids is evidenced by the occurrence of very similar hydrocarbon-bearing vein mineralizations in a wider area.     

Helium and oxygen isotope analyses of hydrothermal fluids from the East Pacific Rise between 17°S and 19°S

 Hydrothermal vent fields south of the Garret Fracture zone were sampled for the isotope composition of helium and oxygen ([¹⁸O]H₂O/[¹⁶OH₂O). The helium isotopes end-member (³He / ⁴He=8.3×R _a and [⁴He]≈1.2–2.4×10^-5 cm³ STP g^-1) is quite similar to other known hydrothermal sites pointing to the homogeneous helium composition of the upper mantle. The δ¹⁸O end-member value (δ¹⁸O≈0.5–0.6‰) confirms previous suggestions from other sites and from isotope modeling, that hydrothermal fluids are slightly enriched in ¹⁸O relative to the ocean as a result of water–rock interactions at high temperature. Received: 11 December 1995/Revision received: 20 December 1996     

Photochemical production of ammonium and transformation of dissolved organic matter in the Baltic Sea

The release of ammonium from the photochemical degradation of dissolved organic matter (DOM) has been proposed by earlier studies as a potentially important remineralisation pathway for refractory organic nitrogen. In this study the photochemical production of ammonium from Baltic Sea DOM was assessed in the laboratory. Filtered samples from the Bothnian Bay, the Gulf of Finland and the Arkona Sea were exposed to UVA light at environmentally relevant levels, and the developments in ammonium concentrations, light absorption, fluorescence and molecular size distribution were followed. The exposures resulted in a decrease in DOM absorption and loss of the larger sized fraction of DOM. Analysis of the fluorescence properties of DOM using parallel factor analysis (PARAFAC) identified 6 independent components. Five components decreased in intensity as a result of the UVA exposures. One component was produced as a result of the exposures and represents labile photoproducts derived from terrestrial DOM. The characteristics of DOM in samples from the Bothnian Bay and Gulf of Finland were similar and dominated by terrestrially derived material. The DOM from the Arkona Sea was more autochthonous in character. Photoammonification differed depending on the composition of DOM. Calculated photoammonification rates in surface waters varied between 121 and 382 μmol NH₄⁺ L^− 1 d^− 1. Estimated areal daily production rates ranged between 37 and 237 μmol NH₄⁺ m^− 2 d^− 1, which are comparable to atmospheric deposition rates and suggest that photochemical remineralisation of organic nitrogen may be a significant source of bioavailable nitrogen to surface waters during summer months with high irradiance and low inorganic nitrogen concentrations.     

Rare earth elements in bottom sediments of major rivers around the Yellow Sea: implications for sediment provenance

Rare earth elements (REEs) of 91 fine-grained bottom sediment samples from five major rivers in Korea (the Han, Keum, and Yeongsan) and China (the Changjiang and Huanghe) were studied to investigate their potential as source indicator for Yellow Sea shelf sediments, this being the first synthetic report on REE trends for bottom sediments of these rivers. The results show distinct differences in REE contents and their upper continental crust (UCC)-normalized patterns: compared to heavy rare earth elements (HREEs), light rare earth elements (LREEs) are highly enriched in Korean river sediments, in contrast to Chinese river sediments that have a characteristic positive Eu anomaly. This phenomenon is observed also in primary source rocks within the river catchments. This suggests that source rock composition is the primary control on the REE signatures of these river sediments, due largely to variations in the levels of chlorite and monazite, which are more abundant in Korean bottom river sediments. Systematic variations in ΣLREE/ΣHREE ratios, and in (La/Yb)–(Gd/Yb)_UCC but also (La/Lu)–(La/Y)_UCC and (La/Y)–(Gd/Lu)_UCC relations have the greatest discriminatory power. These findings are consistent with, but considerably expand on the limited datasets available to date for suspended sediments. Evidently, the REE fingerprints of these river sediments can serve as a useful diagnostic tool for tracing the provenance of sediments in the Yellow Sea, and for reconstructing their dispersal patterns and the circulation system of the modern shelf, as well as the paleoenvironmental record of this and adjoining marginal seas.     

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.     

冲绳海槽中段沉积物物源识别及其热液活动指示

冲绳海槽中段热液活动区表层沉积物的主、微量和稀土元素分析结果表明:区内沉积物主要由陆源物质与热液源物质组分组成,Hg、Au、Sb、Cu、Pb、Zn、Ba、As、Fe和Co等微量元素富集;沉积物的化学风化程度中等,A-CN-K图解表明其暂未受到钾交代影响,且其母岩成分接近花岗闪长岩;北美页岩标准化稀土配分模式曲线整体较为平坦,轻重稀土分馏较弱,部分样品具有与热液流体类似的明显正铕异常.受热液活动影响,部分沉积物中的Fe、Cu、As、Pb和Zn显著富集,结合样品所处站位,整体显示含金属沉积物-过渡沉积物-正常沉积物的空间分配模式.结合(La/Sm)N、(La/Yb)N比值指示区内沉积物的陆源物质主要来自于黄河与台湾岛河流.     

Characteristics of manganese micronodules as indicators of sedimentation conditions in pelagic sediments

Pelagic sediments from three cores in the northern tropical Pacific zone (the northeast basin) have been analyzed for particle size and composition, as well as for number, mass and the distribution of protosyngenetic authigenic manganese micronodules (MN) in them. The sequences are represented by Quaternary carbonate-free clayey–radiolarian, radiolarian–clayey oozes, miopelagic clays, sometimes enriched in radiolarians, pre-Pleistocene miopelagic and eupelagic clays, zeolite–clayey sediments, and zeolitites. Based on factual data (volume of wet sediment, weight of dry sediment and micronodules, their number and proportions of four fractions, the contribution of MN in sediment, and others), the values of different parameters were calculated. The obtained parameters are statistically similar, which allowed us to reveal background and anomalous horizons of sediments and to assume their sedimentation conditions. Similar values of Р_MN/N_MN, Р_fr > 0.05 mm, Р_MN/Р_sed and the mass of micronodules suggest that precisely these parameters reflect the main variations in conditions of pelagic sedimentation.     

Temporal variability in the composition and abundance of terrestrially-derived dissolved organic matter in the lower Mississippi and Pearl Rivers

Here we report on temporal changes in the concentration and composition of lignin phenols in high molecular weight (< 0.2 μm, > 1 kDa) dissolved organic matter (HMW DOM) collected from the lower Mississippi and Pearl Rivers (MR and PR) (USA). Monthly water samples were collected at a station in the lower reach in each river from August 2001 to August 2003. Significantly higher concentrations of lignin and Λ₈ values (mg lignin phenols in 100 mg organic carbon) in the Pearl River than in the Mississippi River, reflected sporadic inputs of terrestrial DOM during rainstorm events from wetlands and forest soils. Larger seasonal variations in lignin concentration and composition in the Pearl River, compared to the Mississippi River, were attributed to shifts in organic matter sources from topsoil inputs during rainstorm events to groundwater inputs and in situ production during base flow in this small river. Conversely, lower Λ₈ and vanillic acid to vanillin ratios [(Ad/Al)v] in the HMW DOM of the lower Mississippi River may be a result of a lower export rate of lignin from agricultural soils due to lower carbon storage in the expansive agricultural systems of the Mississippi River watershed, as well as dilution of phytoplankton DOM inputs. Large seasonal changes in lignin concentration and Λ₈ (linked at times with river discharge), and minimal variability in the composition of lignin phenols, likely represented an integrated signal of soil-derived vascular inputs from the upstream drainage basin. If we are to better understand the controls of organic matter delivery to the coastal zone from both small and large rivers, sampling strategies need to be adjusted to account for the different scales of hydrologic response time and in situ processing associated with different residence times.     

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.     

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).