Reference sediment core and paleogeography of the underwater Slupsk river foredelta in the Baltic Sea

Core Psd-590 (length 947 cm, water depth 124 m) penetrated the entire sequence of marine (Littorina) mud (730 cm) and stopped in gray lacustrine (Ancylus) clays with hydrotroilitic films. The Littorina mud is gray-colored, microlaminated in the interval of 730 to 700 cm, and dark gray with hydrotoilitic films and obscure microlamination higher in the section. According to the diatom data, typical marine sediments begin at the level of 620 cm, while the lithological-geochemical data indicate this change at the level of 730 cm. This level is marked by a considerable increase in the concentrations of SiO_2amorph, CO₂, C_org, and Mn in the sediments. In the interval of 730 to 620 cm, diatoms are represented by both freshwater and brackish-water species. The Littorina transgression began in the form of individual flows of saline North Sea waters into the Baltic Sea, which is evident from the microlamination and sharp peaks in the concentrations of the chemical elements. The transgression exhibits two weakening and one strengthening (core interval of 380 to 220 cm) stages; the latter was marked by the maximal water salinity. The post-Littorina mud contains molluscan shells and fish bones and is enriched in the fraction of 0.05–0.01 mm. The microlaminated Littorina mud was deposited during periods with stagnant conditions in the bottom water layer, while the homogenous sediments accumulated during periods of its aeration.     

Review of recent advances in the interpretation of eastern Mediterranean sapropel S1 from geochemical evidence

The sediments of the eastern Mediterranean basin contain C_org-enriched layers (sapropels) interbedded with the C_org-poor sediments which form by far the greater part of the record. While it is generally appreciated that different surface ocean productivity and bottom water conditions are necessary for the formation and preservation of these two sediment types, less attention has been paid to diagenetic effects which are an expected consequence of transitions between dramatically different bottom water oxygenation levels. A geochemical interpretation has emerged of post-depositional oxidation of the most recent sapropel (S1), initially based on the relationship of the Mn, Fe, C_org and S concentration/depth profiles observed around S1, and the characteristic shapes of these elemental profiles known from other situations. This indicates that post-depositional oxidation has removed approximately half of the visual evidence of the sapropel (∼6 cm from a total of ∼12 cm in the deep basin). The oxidation interpretation from redox-sensitive element redistribution profiles has subsequently been consolidated with evidence from pore water (O₂, NO⁻₃, Mn²⁺ and Fe²⁺) studies, from characteristic solid phase Ba profiles which yield palaeoproductivity records, and from oxidation-sensitive indicator trace elements (I and Se). So far, these geochemical observations have been concentrated in the deeper central parts of the basin, where sediment accumulation rates are lower than on the basin margins, and radiocarbon dating indicates that S1 formation occurred between 5.3 and 9.0 ky (uncorrected conventional radiocarbon time). It remains to be demonstrated whether or not these times are applicable to the entire E. Mediterranean basin. The implications of these findings to guide sampling in future work on the S1 productivity episode and on older sapropels for palaeoenvironmental investigations are discussed.     

Organic geochemical characterization of Santonian to Early Campanian organic matter-rich marls (Sondage No. 1 cores) as related to OAE3 from the Tarfaya Basin,Morocco

In addition to previously analyzed sediments of Cenomanian to Santonian age in the Tarfaya Sondage No. 2 well, this study presents the results of a stratigraphically younger interval of Santonian to Early Campanian age in the adjacent well Tarfaya Sondage No. 1. This interval is part of the oceanic anoxic event 3 (OAE3), which occurred mainly in the Atlantic realm. Due to known high quality source rocks related to OAEs (i.e. Cenomanian–Turonian), the investigated sample section was tested for the quality, quantity and kind of organic matter (OM), describing also the depositional environment. The study was carried out by means of (i) elemental analysis (C_org, CaCO₃, TS), (ii) Rock–Eval pyrolysis, (iii) vitrinite reflectance measurements, (iv) gas chromatography-flame ionization detection (GC-FID) and (v) GC-mass spectrometry (GC–MS). Total content of organic carbon (C_org), values for the hydrogen index (HI) (mainly in the range 500–700 mg/g C_org) and S₂ values (10–40 mg/g rock), support the assumption of a high petroleum generation potential in these Upper Cretaceous sediments. TS/C_org ratios as well as pristane/phytane ratios indicate variable oxygen contents during sediment deposition, representing a typical depositional setting for the Late Cretaceous and are in good agreement with previously analyzed data in the Tarfaya Basin. Phyto- and zoo-plankton were identified as marine sourced. All of the investigated Early Campanian and Santonian samples are immature with some tendencies to early maturation. These results are based on vitrinite reflectance (0.3–0.4% VR_r), T_max values (409–425 °C), production indices (PI; S₁/(S₁ + S₂)< 0.1) and n-alkane ratios (i.e. carbon preference index). As the deposition of these sediments is time related to OAE3, the depositional environment was characterized by oxygen-deficiency or even anoxic bottom water conditions. This situation was favored during the Cretaceous greenhouse climate by limited oxygen solubility in the then warmer ocean water. Furthermore, local factors related to nutrient supply and primary bioproductivity led to the exceptionally thick, Upper Cretaceous organic matter-rich sedimentary sequence of the Tarfaya Basin.     

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.     

GEOCHEMISTRY OF Si, Al, Fe AND CaCO3 IN SEDIMENTS FROM THE CENTRAL PACIFIC

In sediments of the Central Pacific, water depth is the controlling factor of the distribution of Si, Al, Fe and CaCO, .In the shallow and subabysmal areas, CaCO3 content is much greater than that in the abysmal areas where Si, Al and Fe contents are much lower than those in shallow and subabysmal areas. The contents of Si, Al, and Fe increase and that of CaCO3 decrease with the variation of grain size of sediments from coarse to fine. The contents of Al, Si, and Fe are positively related to each other and the content of CaCO3 is negatively related to that of the three elements. The evident regularities of the distribution of Si, Al, Fe and CaCO, in the sediments have revealed to a certain extent that they may be used as the environmental indicators in some cases.     

渤海湾表层沉积物元素地球化学分布特征与影响因素

对取自渤海湾的307个表层沉积物进行了元素测试和粒度分析。渤海湾表层沉积物的常微量元素呈现4种组合:富集于粗粒沉积区的SiO_2、Na_2O亲碎屑元素组合;富集于细粒沉积区的以Al_2O_3和重金属元素为代表的亲黏土元素组合;与缺氧环境有关的MnO、V、TOC元素组合和与河流输入有关的陆源CaO、TiO_2元素组合。粒度粗细主导了渤海湾元素含量分布的整体格局;海域河流物源供应不同较大影响了渤海湾南部(富Na_2O、CaO和SiO_2)和北部(富Ba和P_2O_5)在元素含量上的差异;高流速潮流对海底的冲刷再分配导致曹妃甸南侧Sr、Ca元素的条带状富集异常;有机质在细粒沉积区的富集导致缺氧环境的形成和K_2O、Mn、V、自生黄铁矿的海洋自生化学沉积;人类活动导致以Pb为代表的重金属污染在河流入海口、港口及沿岸海域的元素分布异常;曹妃甸沙坝内侧的泻湖(海洋钙质生物沉积)与沙坝外侧水下岸坡(陆源碎屑沉积)的截然不同的物源,导致了独特地貌沉积环境下元素分布的局部差异。     

Geochemical peculiarities of sediments in the northeastern Black Sea

We present the results of chemical determinations of Al, Fe, Mn, Cu, Ni, Co, Cr, Pb, Sb, and As in Black Sea sediments over a profile from the Kerch Strait to the eastern part of a deep depression (2210 m). The lithological and geochemical variations were studied in the horizontal and vertical profiles of sediments up to 3 m thick. The tendencies in the distributions of the studied metals during Pleistocene and Holocene sedimentation were analyzed beginning from Neoeuxinian freshwater deposits via the overlaying Drevnechernomorian beds with elevated contents of sapropel to modern clayey carbonate deposits with coccolithophorids. Statistical factor analysis isolated five factors: two main factors (75% of the total dispersion) and three subordinate factors. The first leading biogenic factor (47% of dispersion) reflects the correlation between С_org, Cu, and Ni; the second terrigenous factor (28% of dispersion) combimes Fe, Al, Cr, and Sb. The chemical composition of the sediments reflects the manifestation of diagenesis of landslide processes and mud volcanism along with sedimentation regularities.     

Transformation of suspended particulate matter into sediment in the Kara Sea in September of 2011

The biogeochemical processes participating in the transformation of the particulate matter into sediment along the Yenisei River-St. Anna Trough (Kara Sea) meridional profile were studied using hydrochemical, geochemical, microbiological, radioisotope, and isotope methods. The water-sediment contact zone consists of three subzones: the suprabottom water, the fluffy layer, and the surface sediment. The total number, biomass, and integral activity of the microorganisms (dark ¹⁴CO₂ assimilation) in the fluffy layer are usually higher than in the suprabottom water and sediment. The fluffy layer shows a decrease in the oxygen content and the growth of the dissolved biogenic elements. It was provided by the particulate organic matter supporting the vital activity of the heterotrophs from the overlying water column and by the flux of reduced compounds (NH₄, H₂S, CH₄, Fe²⁺, Mn²⁺, and others) from the underlying sediments. The C_org isotopic composition of the fluffy layer and the sediments is 2–4 ‰ heavier than that of the particulate matter and sediment due to the presence of the isotopically heavy biomass of microorganisms. A change in the isotopic composition of the C_org in the fluffy layer and surface sediment as compared to the C_org of the particulate matter is a widespread phenomenon in the Arctic shelf seas and proves the leading role of microorganisms in the transformation of the particulate matter into sediment.     

Nitrogen and carbon isotopic composition of marine and terrestrial organic matter in Arctic Ocean sediments:: implications for nutrient utilization and organic matter composition

Relationships between organic carbon, total nitrogen and organic nitrogen concentrations and variations in δ¹³C_org and δ¹⁵N_org are examined in surface sediments from the eastern central Arctic Ocean and the Yermak Plateau. Removing the organic matter from samples with KOBr/KOH and determining residual as well as total N shows that there is a significant amount of bound inorganic N in the samples, which causes TOC/N_total ratios to be low (4–10 depending on the organic content). TOC/N_org ratios are significantly higher (8–16). This correction of organic TOC/N ratios for the presence of soil-derived bound ammonium is especially important in samples with high illite concentrations, the clay mineral mainly responsible for ammonium adsorption. The isotopic composition of the organic N fraction was estimated by determining the isotopic composition of the total and inorganic nitrogen fractions and assuming mass-balance. A strong correlation between δ¹⁵N_org values of the sediments and the nitrate concentration of surface waters indicates different relative nitrate utilization rates of the phytoplankton in various regions of the Arctic Ocean. On the Yermak Plateau, low δ¹⁵N_org values correspond to high nitrate concentrations, whereas in the central Arctic Ocean high δ¹⁵N_org values are found beneath low nitrate waters. Sediment δ¹³C_org values are close to −23.0‰ in the Yermak Plateau region and approximately −21.4‰ in the central Arctic Ocean. Particulate organic matter collected from meltwater ponds and ice-cores are relatively enriched in ¹³C (δ¹³C_org=−15.3 to −20.6‰) most likely due to low CO₂(aq) concentrations in these environments. A maximum terrestrial contribution of 30% of the organic matter to sediments in the central Arctic Ocean is derived, based on the carbon isotope data and various assumptions about the isotopic composition of the potential endmembers.     

Geochemical and textural properties of carbonate and terrigenous sediments along the Jordanian coast of the Gulf of Aqaba

The physicochemical properties of 21 marine sediment samples were investigated, collected from five different localities along the Jordanian coast of the Gulf of Aqaba. According to the chemical parameters, sediments were categorized into three groups: carbonate (80% CaCO₃), composed mainly of materials of calcareous skeletal structures; terrigenous (<10% CaCO₃) depositional areas for land-derived materials from surrounding rocks and alluviums; and a admixture of the first two (19–37% CaCO₃). High significant linear correlations were found between organic carbon (OC) and total nitrogen (TN), indicating the occurrence of these components in a common phase (organic matter). Despite the co-occurrence of TP in organic matter, these two elements were negatively correlated, indicating anthropogenic sources of pollution such as phosphate exportation (hotel areas and clinker port sites) and industrial activities (industrial complex site). The study found that variations in texture properties and mud contents were due to differences in sediment sources, topography and their response during currents and waves. The finer, well-sorted sediments contain lower elemental concentrations of OC, calcium carbonate and TN (excluding TP) than coarser, poorly-sorted sediments.     

The key features of the bottom sediment composition in the anoxic Lake Mogil’noe

In the summer 2006, integrated geological, geochemical, hydrological, and hydrochemical studies were performed on the relict anoxic Lake Mogil’noe (down to 16 m depths) located on Kil’din Island in the Barents Sea. The chemical and grain-size composition of the bottom sediments were compared for the lake (a permanently anoxic basin) and the Baltic Sea Deeps (periodically anoxic basins). The vertical location of the hydrogen sulfide layer boundary in the lake (9–11 m depths) was practically the same from 1974 up to now. The concentrations of suspended particulate matter in the lake in June and July 2006 appeared to be close to its summer concentrations in the seawaters of the open part of the Baltic Sea. The mud from Lake Mogil’noe compared to those of the Baltic Sea Deeps are characterized by fluid and flake consistency and by pronounced admixtures of sandy and silty fractions probably of eolic origin. The lacustrine mud contain much plant remains; iron sulfides and vivanite were also found in ooze. The concentrations of 22 elements determined in the lacustrine bottom sediments were of the same levels as those found here 33 years ago. The concentrations also appeared to be close to those in the corresponding grain-size types of the bottom sediments in the Baltic Sea. The low C_org/N value (5% on average) in the mud of Mogil’noe Lake compared to the values for the mud of the Baltic Sea Deeps (10% on average) points to the considerable planktogenic component in the organic matter composition of the lacustrine mud. No indications were reveled for anthropogenic contaminations of the lacustrine bottom sediments with toxic metals.     

Phosphorus regeneration and burial in near-shore marine sediments (the Gulf of Trieste, northern Adriatic Sea)

According to bioassay studies and high dissolved nutrient N/P ratios in the seawater column, phosphorus (P) is thought to control marine productivity in the northern Adriatic Sea. P in near-shore marine sediments of the Gulf of Trieste, the northernmost part of the Adriatic Sea, was investigated using pore water P distributions, and benthic P flux studies under oxic and anoxic conditions. The data show that P regeneration is up to three-fold more extensive in sediments overlain by oxygen-depleted waters and proceeds in parallel with Fe and Mn enhanced benthic fluxes. It appears from the incubation experiments that degradation of sedimentary organic matter is the main contribution to the flux of P at the sediment–water interface, while the release of phosphate adsorbed on the iron oxide surface is of minor importance.It appears that about 50% of P in the Gulf of Trieste is retained within in the sediments, probably bonded to clay minerals and carbonate grains or precipitated as fluoroapatite. In these sediments total P (P_tot) is preserved preferentially over organic C (C_org). P regenerated from surficial sediments contributes about 1/3 of the P that is assimilated by benthic microalgae. The phytoplankton P requirement should be entirely supplied from fresh-water sources. These results suggest that oxygen depletion in coastal areas caused by eutrophication enhances P regeneration from sediments, providing the additional P necessary for increased biological productivity. The development of anoxic bottom waters in coastal areas enhances the recycling of P, exacerbating the nutrient requirement in the area. A geochemical record of P burial in a longer sedimentary sequence revealed an increasing trend of P_tot and organic P (P_org) contents occurring approximately 50 years BP (after 1950), probably due to increasing use of inorganic fertilizers and detergents in the area.     

The origin and biogeochemistry of organic matter in surface sediments of Lake Shihwa and Lake Hwaong

To understand the origin and biogeochemistry of the organic matter in surface sediments of Lake Shihwa and Lake Hwaong, organic nitrogen, inorganic nitrogen, labile organic carbon, and residual organic carbon contents as well as stable isotope ratios for carbon and nitrogen were determined by KOBr-KOH treatment. Ratios of organic carbon to organic nitrogen (C_org/N_org) (mean = 24) were much higher than ratios of organic carbon to total nitrogen (C_org/N_tot) (mean=12), indicating the presence of significant amounts of inorganic nitrogen in the surface sediments of both lakes. Stable isotope ratios for organic nitrogen were, on average, 5.2‰ heavier than ratios of inorganic nitrogen in Lake Shihwa, but those same ratios were comparable in Lake Hwaong. This might be due to differences in the origin or the degree of degradation of sedimentary organic matter between the two lakes. In addition, stable isotope ratios for labile organic carbon were, on average, 1.4‰ heavier than those for residual organic carbon, reflecting the preferential oxidation of¹³C-enriched organic matter. The present study demonstrates that KOBr-KOH treatment of sedimentary organic matter can provide valuable information for understanding the origin and degradation state of organic matter in marine and brackish sediments. This also suggests that the ratio of C_org/N_org and stable isotope ratios for organic nitrogen can be used as indexes of the degree of degradation of organic matter.     

Benthic remineralization and burial of biogenic SiO2, CaCO3, organic carbon, and detrital material in the Southern Ocean along a transect at 170° West

We investigated the composition, recycling, and mass accumulation rates of sediments along a transect in the Southern Ocean located from 66°S to 57°S at 170°W. This transect also corresponds to the location of a sediment trap mooring line. The sediments at the seven sites studied range from largely terrigenous material to nearly pure (>90%) biogenic silica. CaCO₃ is a minor but persistent component at most sites. Mass accumulation rates have been determined on the basis of excess ²³⁰Th in the sediments, i.e., ²³⁰Th-normalized accumulation rates. The influence of redistribution of sediments on the sea floor has been estimated from ¹⁴C analyses. The recycling of material delivered to the sediments has been characterized on the basis of pore water studies that make extensive use of both in situ sampling and shipboard extractions. The influence of the highly variable rates of input of particulate matter that characterize much of the Southern Ocean upon pore water gradients and fluxes across the sediment water interface has been considered.We find only poor correspondence between BSiO₂ burial fraction (=burial/particulate flux), a quantifiable measure of preservation efficiency, and BSiO₂ particulate rain along the transect. However, preservation does appear to be closely linked to a combination of sedimentation rate and particulate rain.The burial fraction of BSiO₂ is small relative to benthic rain (5–19%). Despite the small fraction buried, burial flux normalized to (sedimentation rate)^1/2 appears to provide a very consistent means of predicting benthic particulate rain over a large range of rain rates, including data from a number of different studies and environments. At sites with BSiO₂ rain 250 mmol m⁻² yr⁻¹ the average difference between predicted and observed rain is 25–30%. Such rain rates occur in many marine areas, particularly the Southern Ocean, with the result that this relationship potentially provides a means of estimating BSiO₂ benthic rain over prolonged periods in the past on the basis of readily measured sediment parameters.At the southern-most deep ocean station, the particulate flux was characterized by an extremely high C_org/CaCO₃ ratio (>10), but this high ratio does not appear to have a substantial influence on CaCO₃ burial. CaCO₃ is preserved in the sediments at this site despite a particulate flux with a 10-fold excess of C_org above that required for complete dissolution in the sediments. The unexpectedly high preservation of CaCO₃ is due largely to the very steep C_org oxidation rate profile at this site. As a result, a large fraction of the organic matter oxidized in the sediments does so in close proximity to the sediment–water interface where most of the metabolic CO₂ is neutralized by CO₃²⁻ from the overlying water, rather than by the dissolution of sedimentary CaCO₃.Diagenetic modeling indicates that at several of the stations, the remineralization fluxes of carbonate species across the sediment–water interface may not have been at steady state as a result of the highly pulsed nature of particulate rain in this environment. We estimate that at the time of our sampling it is possible that near-interface fluxes could have been a factor of 1.6–2 times the annual average.At every site on the transect, the burial fluxes of detrital material are substantially greater than the detrital particulate rain measured in the sediment traps, by as much as a factor of 40. Detrital burial is bimodal, being greatest at the southern and northern extremes of the transect. We postulate that the excess of burial over particulate rain in the south reflects the contribution of ice rafted debris at these high latitudes. Increases in the supply at the northern stations must have a different source. We believe that the excess at these stations is material eroded from the sea floor to the west, possibly on the Campbell Plateau, and advected by currents to the northern portion of the transect at depths below the shallow traps.     

Carbonate removal by acidification causes loss of nitrogenous compounds in continental margin sediments

This study reports on measurements of organic carbon (C_org) and total nitrogen (N_tot) in surface sediments originating from 6 transects along the northwest European continental margin. After elimination of carbonates by an acidification technique using sulphurous acid, both elements were analysed in the same sediment sample using an elemental analyser. C_org and N_tot in the sample were comparatively low, ranging between 1 and 10 mg C and 0.2 to 1 mg N g⁻¹ dry sediment. In a second analysis, the samples were analysed without acid addition, resulting in N_tot concentrations of 0–50% higher compared to their acidified counterparts. As a consequence, molar C/N ratios derived from the analysis of C_org and N_tot in the acidified sample ranged between 6 to 11, while the N_tot separate analysis reduced C/N ratios to 6 to 8. It is suggested that the addition of sulphurous acid to eliminate inorganic carbon volatilises nitrogenous organic matter.     

Spatial distribution of microelements in the seston of the White Sea

With a view to a more complete understanding of the role of phyto-and zooplankton in biogeochemical cycles, the spatial distributions of Fe, Mn, Co, Ni, Cr, Cu, Cd, Pb, Zn, As, Hg, and C_org in the White Sea seston (21 samples) collected in August 2004 during cruise 64 or R/V Professor Shtokman were studied. It was shown that the elements studied are accumulated in plankton with enrichment coefficients from 10² for Hg to 10⁵ for Fe, as compared to seawater. The spatial distribution of microelements is determined by the sources of their supply and correlates with the distribution of the primary production and biomass of zooplankton. The increased values of microelement contents (excluding As) are characteristic of Dvina Bay, whereas the highest As concentrations were found in Kandalaksha Bay.     

Palynology and geochemistry of channel-margin sediments across the tidal–fluvial transition,lower Fraser River,Canada: Implications for the rock record

In the tidally influenced Fraser River, Canada, palynological and carbon isotope (δ¹³C_org) signatures of channel-margin sediments are compared to environmental parameters (e.g., grain size, water salinity) to establish how the signatures vary across the tidal–fluvial transition. Palynological assemblages in the Fraser River are dominated by tree pollen, which constitutes between 85% and 95% of all assemblages. Dinocyst abundances do not exceed 2% of the total palynological assemblage, and the number and diversity of dinocysts gradually decreases landward. The calculated landward limit for dinocysts is at approximately 83 river km, which is relatively close to the upstream limit of the tidal backwater (at ∼100 km). δ¹³C_org values show minimal variability across the tidal–fluvial transition, and the average value is approximately −26‰. The δ¹³C_org signature of river sediments indicates a dominance of terrestrially sourced organic matter regardless of brackish-water and tidal influence on sediment deposition.Six palynological and geochemical trends are identified as relevant to the rock record. 1) In deltaic environments, palynological and geochemical characteristics are less useful than sedimentological and ichnological characteristics for establishing depositional conditions. 2) In marginal-marine settings, low abundances and low species diversities of dinocysts, coupled with a “terrestrial” geochemical signature (δ¹³C_org < −25‰) do not necessarily indicate deposition in a terrestrial environment. 3) Dinocyst abundances above 1% of the total palynomorph population can indicate a significant marine influence on sediment deposition. 4) Mud beds, preferably bioturbated, should be preferentially sampled in order to maximize palynomorph recovery. 5) Marine palynomorphs can occur, albeit in very low concentrations, to the landward limit of the tidal–backwater zone. 6) Palynological and geochemical data should be compared across the paleo-depositional environment in order to establish general trends and remove local variations caused by biases such as grain size.     

The geochemistry of deepwater particulate matter over the hydrothermal field at 9°d50′ N (the East Pacific Rise)

The results of geochemical studies of particulate matter in the water mass over the hydrothermal field at 9°50′ N on the East Pacific Rise are presented. The particulate matter was tested in background waters, in the buoyant plume, and in the near-bottom waters. The contents of Si, Al, P, C_org, Fe, Mn, Cu, Zn, Ni, Co, As, Cr, Cd, Pb, Ag, and Hg were determined. No definite correlations were found between the ele-ments in the background waters. Many of the chemical elements correlated with Fe and associated with its oxyhydroxides in the buoyant plume. In the near-bottom waters, microelements are associated with Fe, Zn, and Cu (probably, to their sulfides formed under fluid mixing with seawater). The matter precipitated in a sed-imentation trap was similar to the near-bottom particulate matter in the elemental composition.     

用细化的铁形态分析及量化的铁氧化物活性表征海洋沉积物中铁的成岩作用：以胶州湾为例

以富营养化的胶州湾一个柱状沉积物为例,用细化的铁形态分析及量化的铁氧化物还原活性相结合的方法研究了沉积物中铁的成岩作用过程。结果表明,这两种方法相结合的结果能更详细示踪铁的转化并能从多视角提供铁成岩作用的细微差别。这一方法有望应用于其它研究中更好地揭示复杂的铁和硫的生物地球化学循环。铁微生物还原在上部沉积物铁的还原中起重要作用,但12 cm深度以下铁被硫化物的化学还原为主要过程。最具生物活性的无定形铁氧化物是铁微生物还原的主要参与者,然后依次为弱晶态铁氧化物和磁铁矿,晶态铁氧化物几乎不参与铁的成岩循环。沉积物上部铁微生物还原的重要作用主要是活性铁含量高而活性有机质含量低共同作用的结果,且后者也是沉积物中硫酸盐还原速率以及硫化物积累的最终制约因素。对比研究表明,通过还原性溶解动力学方法表征的微生物可还原的铁氧化物主要由无定形和弱晶态铁氧化物组成,其总体活性常数相当于老化的水铁矿,且随深度增加而减低。     

Late Cretaceous (Late Turonian,Coniacian and Santonian) petroleum source rocks as part of an OAE,Tarfaya Basin,Morocco

Late Turonian, Coniacian and Santonian source rock samples from a recently drilled well (Tafaya Sondage No. 2; 2010) in the Tarfaya Basin were analyzed for quantity, quality, maturity and depositional environment of the organic matter (OM). To our knowledge such a thick sequence of organic matter-rich Turonian to Santonian source rocks was investigated in that great detail for the first time. Organic geochemical and organic petrological investigations were carried out on a large sample set from the 200 m thick sequence. In total 195 core samples were analyzed for total organic carbon (C_org), total inorganic carbon contents and total sulfur (TS) contents. Rock-Eval pyrolysis and vitrinite reflectance measurements were performed on 28 samples chosen on the basis of their C_org content. Non-aromatic hydrocarbons were analyzed on selected samples by way of gas chromatography–flame ionization detection (GC–FID) and GC–mass spectrometry (GC–MS). The organic matter-rich carbonates revealed a high source rock potential, representing type I kerogen and a good preservation of the organic matter, which is mainly of marine (phytoplankton) origin. HI values are high (400–900 mg/g C_org) and in a similar range as those described for more recent upwelling sediments along the continental slope of North Africa. TS/C_org ratios as well as pristane over phytane ratios indicate variable oxygen content during sediment deposition. All samples are clearly immature with respect to petroleum generation which is supported by maturity parameters such as vitrinite reflectance (0.3–0.4%), T_max values (401–423 °C), production indices (S₁/(S₁ + S₂) > 0.1) as well as maturity parameters based on ratios of specific steranes and hopanes.