Chemical and isotopic evidence for the nature of the fluid in CH4-containing sediments of the Håkon Mosby Mud Volcano

The pore waters of CH₄-containing sediments of the Håkon Mosby Mud Volcano were rich in NH⁺ ₄, Br^-, and I^-; exhibited a high total alkalinity; but were poor in Cl^-and SO^2- ₄. The geological evidence and our data suggest that organic matter decomposition in preglacial or early interglacial sediments took place during early diagenesis (bacterial processes) and during metamorphism (thermogenic processes under the 3100-m-thick layer of glacial sediments), accompanied by mud volcano fluid generation. It is argued that the CH₄of the mud volcano sediments has a mixed, biogenic and thermogenic, origin.     

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.     

Geoacoustic and physical properties of carbonate sediments of the Lower Florida Keys

 Near-surface sediment geoacoustic and physical properties were measured from a variety of unconsolidated carbonate sediments in the Lower Florida Keys. Surficial values of compressional and shear speed correlate with sediment physical properties and near-surface acoustic reflectivity. Highest speeds (shear 125–150 m s^-1; compressional 1670–1725 m s^-1) are from sandy sediments near Rebecca Shoal and lowest speeds (shear 40–65 m s^-1; compressional 1520–1570 m s^-1) are found in soft, silty sediments which collect in sediment ponds in the Southeast Channel of the Dry Tortugas. High compressional wave attenuation is attributed to scattering of acoustic waves from heterogeneity caused by accumulation of abundant shell material and other impedance discontinuities rather than high intrinsic attenuation. Compared to siliciclastic sediments, carbonate sediment shear wave speed is high for comparable values of sediment physical properties. Sediment fabric, rather than changes due to the effects of biogeochemical processes, is responsible for these differences.     

Bacterial iron oxide reduction in a terrigenous sediment-impacted tropical shallow marine carbonate system, north Jamaica

Discovery Bay, a carbonate-dominated embayment in north Jamaica, has been subject to inputs for 40 years of iron-rich bauxite sediment associated with the local mining and transport of processed bauxite. As such, this site is an ideal natural laboratory to study the records and impacts of iron oxide inputs upon geochemical, diagenetic, and microbial processes in tropical carbonate sediments.Total Fe contents in sites in the bay not receiving bauxite inputs are negligible and porewater Ca²⁺, SO₄²⁻ and Cl⁻ indicate that bacterial sulphate reduction is an important process. In contrast, surface sediments receiving bauxite inputs contain significant total Fe, from 44 μmol/g in shallow (5 m water depth) sites to 110 μmol/g in deeper (20 m water depth) sites. Up-core increases in total Fe record increased temporal inputs into the bay. Within these Fe-rich sediments porewater data shows the presence of Fe^II released by bacterial Fe^III reduction. There is no direct evidence for significant bacterial sulphate reduction in these sediments. Iron oxides within all bauxite-impacted sediments display a high potential reducibility, from 40% to 80% of the total Fe present as dithionite-extractable Fe^III. Experimental analysis of the potential susceptibility to, and rates of, bacterial Fe^III reduction, utilising Discovery Bay sediment and Shewanella putrefaciens CN32 (a known Fe^III-reducer) has confirmed the high bacterial reducibility of iron oxides within the sediment. Up to 75% of initial dithionite-extractable Fe^III in the sediments was reduced over 15 days.The presence of iron oxides within the Discovery Bay shallow marine carbonate systems has markedly altered the chemical diagenetic processes taking place, with a shift from apparent dominance of bacterial sulphate reduction at non-impacted (Fe-poor) sites, to highly significant bacterial Fe^III reduction in Fe-rich bauxite-impacted sediments. Given the perceived global increases in terrigenoclastic sediment inputs into tropical carbonate systems as a result of land-use and climate changes, coupled with the documented role that iron oxide reduction plays in nutrient and contaminant cycling in sediment systems, more research into the perturbation of early diagenesis by iron oxide inputs is required.     

Uranium in coastal sediments of Tokyo Bay and Funka Bay

The sediment cores from Tokyo Bay and Funka Bay were analyzed for U and its isotopic ratio,²³⁴U/²³⁸U, after dissolving them in 0.1 M HCl, and 30% H₂O₂ in 0.05 M HCl. A small fraction of U in the anoxic sediments was dissolved in 0.1M HCl and even the added yield tracer,²³²U, was lost. The isotopic ratio of H₂O₂ soluble U in the sediments was equal to that of seawater, suggesting that the H₂O₂ soluble U in the sediments is authigenic. The 6M HCl solution dissolved part of the lithogenic U besides the authigenic U. The depth profiles of U from the two bays resembled each other. The authigenic U comprised more than half of the total U even at the surface and increased with depth down to 70 cm, showing small maxima at about 20 cm. The concentration of refractory U was nearly constant with depth and similar to that of the pelagic sediments. The highest U concentration, 6 µg g^–1 which was about 5 times that of the pelagic sediments, was observed in the layer between 70 and 160 cm depth in Tokyo Bay. The annual sedimentation rates of U in the Tokyo Bay sediments were 2.6 tons at the surface and 7.0 tons at the 70–160 cm depth. The increase in U with depth should be due to the deposition of interstitial U either diffusing downward from the surface indicating the trapping of seawater U, or otherwise diffusing upward from the deeper layer indicating the internal cycling of U within the sediments.     

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.     

Sources of δ15N variability in sinking particulate nitrogen in the Cariaco Basin,Venezuela

Ten years of monthly observations of the δ¹⁵N of sinking particulate nitrogen (δ¹⁵N–PN (in ‰ versus atmospheric N₂)=[(¹⁵N/¹⁴N)_sample/(¹⁵N/¹⁴N)_standard)−1]1000) in the Cariaco Basin, Venezuela, confirm that the basin's bottom sediments store information about nitrogen dynamics related to seasonal and interannual variability in regional surface ocean processes. During the upwelling period of the southern Caribbean Sea (February–April), the δ¹⁵N–PN is similar to that of the thermocline nitrate (∼3.5‰). This nitrate is imported into the Cariaco Basin with Subtropical Underwater (SUW), which wells up near the coast. Thus, particles generated by phytoplankton photosynthesis during this productive period bear a sub-tropical North Atlantic isotopic imprint of N₂ fixation (low compared to the global average of nitrate δ¹⁵N≈5‰). During the non-upwelling period when surface waters are stratified (September–November), the δ¹⁵N–PN is also 3.5–4.0‰, and reflects a mixture of local N₂ fixation within the mixed layer, inputs of terrigenous organic matter and SUW nitrate consumption by phytoplankton below the mixed layer, which most likely exerts the strongest control on the δ¹⁵N–PN signal during this time. In the transition periods of May–July and December–January, the δ¹⁵N–PN increases to 4.5–6.5‰. This coincides with maxima of continental material fluxes (terrestrial PON δ¹⁵N is >6‰) into the Cariaco Basin. The δ¹⁵N signal in the sediments of the Cariaco Basin thus provides information about the relative strength of the local coastal upwelling, the relative input of continental material via river runoff, and local N₂ fixation. The findings contribute to interpretations of the basin's paleoclimatic nitrogen cycle variations based on observations of the sedimentary δ¹⁵N record at this location.     

Sedimentation and mixing rates of radionuclides in Barents Sea sediments off Novaya Zemlya

Radionuclide measurements have been conducted on sediment cores collected in 1992 in the south-eastern region of the Barents Sea, known as the Pechora Sea. Cesium-137 and ^239,24OPu activities in surface sediments are generally less than 30 Bq/kg, with the highest levels being measured in sediments off the southwestern coastline of the island of Novaya Zemlya. High correlations between both ¹³⁷Cs and ^239,24OPu and the concentration of fine (< 63 μm) particles in surface sediments indicate that much of the variance in radionuclide concentrations throughout the Pechora Sea can be explained by particle size fractionation. However, elevated activities of ¹³⁷Cs (138 Bq/kg), ⁶⁰Co (92 Bq/kg), ²⁴¹Am (433 Bq/kg), and especially ^239,24OPu (8.47 × 103 Bq/kg) were measured in one surface sediment sample from the fjord of Chernaya Bay on the southern coast of Novaya Zemlya. The source of radioactive contamination is two underwater nuclear tests conducted in Chernaya Bay in 1955 and 1957.The ²³⁸Pu/^239,240Vu activity ratio of 0.0245 in Chernaya Bay is equivalent to values measured in global fallout. The ²⁴⁰Pu/²³⁹Pu atom ratio (0.0304), measured by mass spectrometry, is much lower than values (0.18) typical of global fallout, but is consistent with ratios measured for fallout from the early (1951–1955) series of weapons tests at the Nevada Test Site. The timing of the Chernaya Bay source term, estimated from the ²⁴¹Am/²⁴¹Pu ratio, is consistent with the timing of the 1955 and 1957 underwater nuclear tests. Relatively low initial yields of ²⁴¹Pu (²⁴¹Pu/²³⁹Pu atom RATIO = 0.00 123) in these tests have resulted in relatively low ²⁴¹Am/^239,240Pu activity ratios (0.05) in recent sediments in Chernaya Bay.Radionuclide tracer profiles in cores from the Pechora Sea can be simulated using a two-layer biodiffusion model with rapid, near-homogeneous mixing in the surface mixed layer and reduced mixing in the deep layer. Lead-210 profiles are consistent with a wide range of sedimentation and mixing rates in the deep sediment layer. However, the ¹³7Cs and ^239,240Pu results further constrain the model parameters and indicate that the downward transport of radionuclides in the sediments is governed primarily by sediment mixing, with sediment burial playing a secondary role.     

Processes affecting long-term changes in <Superscript>137</Superscript>Cs concentration in surface sediments off Fukushima

Temporal changes in cesium-137 (¹³⁷Cs) concentrations in the surface (0–10 cm) layer of seabed sediment were quantified from continuous observation data at 71 stations within a 150-km radius of the Fukushima Daiichi Nuclear Power Plant, and the primary processes affecting temporal changes were identified. From March 2011 to the end of 2015, about 80% of the initially deposited ¹³⁷Cs in the surface sediment in the coastal region (bottom depth ≤100 m) region has dissipated (radioactive decay is not included). Such a remarkable change in the ¹³⁷Cs concentration was not observed in the offshore (>100 m) region. This paper focuses on the following three processes that affected the decrease in the ¹³⁷Cs concentrations, and assesses their relative importance; (1) resuspension and transport of ¹³⁷Cs-bound sediment, (2) desorption of ¹³⁷Cs from the sediment, and (3) dilution of ¹³⁷Cs by vertical mixing of sediment. Consequently, it was estimated that the first two processes together have potentially contributed to reduce the ¹³⁷Cs inventory in the top 10 cm of the coastal region by at most 35%. Furthermore, by applying a pulse input sediment mixing model to the observed vertical distribution of sedimentary ¹³⁷Cs, it was also estimated that more than 43% of the ¹³⁷Cs in the surface sediment was transported to deeper sediment layers by vertical mixing of the sediment. This indicates that the decrease of ¹³⁷Cs concentrations in coastal sediments was mainly affected by mixing of ¹³⁷Cs-bound surface sediment with less contaminated sediment in the deeper layers.     

The transient and steady-state influence of sediment compaction and interstitial water expulsion on the temperature distribution in oceanic sediments

The transient and steady-state solution of the linear heat transfer equation considering the rate of compaction of sediments and the vertical migration of interstitial water are obtained, respectively, for a single layer and a multi-layer model of unconsolidated sediments. At steady state the temperature profile with depth becomes a convex curve rather than a straight line due to the presence of above factors. The time needed to reach the steady state is observed to be directly proportional to the square of the thickness of the layer. The thermal gradient at the surface increases parabolically with the increase in the rate of the above-mentioned factors.The application of the steady-state results to the bore hole in Amchitka Island (Sass and Munroe, 1970) suggests that the observed surface heat flow value differs by 14% from the calculated one. Also the heat flow value at greater depth is calculated to be 2.02 · 10⁶ cal cm ²s¹, which is close to the mean value for Phillippine Trench (Nagasaka et al., 1970).     

Sedimentary nutrient dynamics in a tropical estuarine mangrove ecosystem

Mangrove sediments play a pivotal role in the nutrient biogeochemical processes by behaving as both source and sink for nutrients and other materials. Surface and core sediments were collected from various locations of the Pichavaram mangrove (India) and analyzed for grain size distribution, nutrients and stable N isotope (δ¹⁵N) signatures in order to understand the spatial and vertical distribution of nutrients and biogeochemical processes of the C, N, P and S in this ecosystem. Sand is the dominant fraction followed by silt and clay. Spatial distribution of nutrients is controlled by the external and internal loadings, whereas vertical distribution is largely driven by the in situ microbial activities. Interior mangrove sediments contain higher concentrations of organic carbon (OC) than the estuarine sediments reflecting high rates of organic matter retention. Finer fractions of sediment hold ∼60% OC due to high surface area. At some sampling points, moderately high δ¹⁵N signatures were observed and this may be because of agricultural runoff and aquaculture effluents.     

Bioturbation depths, rates and processes in Massachusetts Bay sediments inferred from modeling of Pb and Pu profiles

Profiles of ²¹⁰Pb and ^{239 + 240}Pu from sediment cores collected throughout Massachusetts Bay (water depths of 36–192 m) are interpreted with the aid of a numerical sediment-mixing model to infer bioturbation depths, rates and processes. The nuclide data suggest extensive bioturbation to depths of 25–35 cm. Roughly half the cores have ²¹⁰Pb and ^{239 + 240}Pu profiles that decrease monotonically from the surface and are consistent with biodiffusive mixing. Bioturbation rates are reasonably well constrained by these profiles and vary from 0.7 to 40 cm² yr⁻¹. As a result of this extensive reworking, however, sediment ages cannot be accurately determined from these radionuclides and only upper limits on sedimentation rates (of 0.3 cm yr⁻¹) can be inferred. The other half of the radionuclide profiles are characterized by subsurface maxima in each nuclide, which cannot be reproduced by biodiffusive mixing models. A numerical model is used to demonstrate that mixing caused by organisms that feed at the sediment surface and defecate below the surface can cause the subsurface maxima, as suggested by previous work. The deep penetration depths of excess ²¹⁰Pb and ^{239 + 240}Pu suggest either that the organisms release material over a range of >15 cm depth or that biodiffusive mixing mediated by other organisms is occurring at depth. Additional constraints from surficial sediment ²³⁴Th data suggest that in this half of the cores, the vast majority of the present-day flux of recent, nuclide-bearing material to these core sites is transported over a timescale of a month or more to a depth of a few centimeters below the sediment surface. As a consequence of the complex mixing processes, surface sediments include material spanning a range of ages and will not accurately record recent changes in contaminant deposition.     

Manganese fluxes to the oceans

Application of a simple model describing regional variations in the contents of manganese and associated minor metals in deep-sea sediments suggests that solid manganese phases are being removed from the <0.5 μm fraction of seawater at ～1–7 · 10¹²g yr^?1 in excess of the rate of stream-supplied manganese. This flux is consistent with: (1) the relative rates of sediment accumulation in the Atlantic and Pacific Oceans; (2) the contrast between the oceanic residence time of manganese calculated from stream-supply data (14 · 10³ yr) and from the flux of manganese precipitating in marine sediments or as manganese nodules (0.38–2.4 · 10³ yr); (3) the surplus mass of manganese revealed by geochemical balance calculations (22.9 · 10²g). On this basis excess manganese is accumulating in deep-sea sediments at 0.2–2.0 · 10^?6 g cm^?2yr^?1. Manganese supplied to the upper layers of marine sediments by diagenesis has been evaluated with the aid of vertical advection—diffusion—reaction models. The calculated diagenetic flux of manganese at the sediment surface in a near-shore environment is in agreement with the known accretion rate of manganese deposits (1.7 · 10^?2 g cm^?2 10^?3 yr^?1) and the regionally variable flux over the area assessed is consistent with the presence or absence of manganese nodules at or near the water-sediment interface. The diagenetic flux at the surface of deep-sea sediments has been calculated at 0.7 · 10^?4 g cm^?2 10^?3 yr^?1 when the upper, oxic, zone of the sediment is ～20 cm thick. A limiting factor on the in situ production flux of dissolved manganese in deep-sea sediments appears to be the availability of reducing agents for manganese dissolution rather than the rate of downward transport of manganese-rich sediment to a reaction boundary where dissolution takes place. Various estimates of the rate of upward-migrating manganese suggest that manganese precipitates in the oxic zone with a rate constant of ～10^?7 sec^?1 with the result that diagenetic processes cannot supply the flux of excess manganese through more than ～0.25 m of oxic sediment. However, estimates of the flux of manganese to the oceans by submarine volcanic processes (0.79–1.1 · 10¹²g yr^?1) are similar to the surplus mass of manganese detected by geochemical balance calculations (0.7 · 10¹²g yr^?1). If submarine hydrothermal solutions provide only 10% of this excess then their computed discharge rate (39 g cm^?2 yr^?1) and residence time in the upper layer of oceanic crust (130,000 yr) agree well with these parameters for continental thermal springs.     

Seasonal dynamics of elemental sulfur in two coastal sediments

A spectrophotometric method for elemental sulfur (S⁰) analysis without interference from other reduced sulfur compounds was adapted for the use in reducing sediments. The S⁰ distribution in two coastal sediments was studied regularly from summer to winter and compared to factors regulating the S⁰ accumulation, such as redox potentials, the rate of bacterial sulfide production and the general sulfur chemistry. Dense coatings of sulfur bacteria developed on the sediment surface of a sulfuretum which had an S⁰ concentration of up to 41 μmol S cm^?3. The 2·5-mm thick bacterial coating contained 40% of all S⁰ in the sediment. A more typical marine sediment with a few cm thick oxidized surface layer had an S⁰ maximum of 1–3 μmol S cm^?3 at 2–4 cm depth. The S⁰ maximum in both sediments increased from summer to winter as the sediments gradually became more oxidized. The deeper layers maintained a low S⁰ concentration. Most of the S⁰ in the upper few mm of a laboratory sulfuretum was present inside sulfur bacteria and actively migrated up and down with the bacteria depending upon the changing light and oxygen conditions.     

南海近海海水中放射性总α、总β的研究

本文对南海近海海水中的放射性总α、总β的含量和分布进行了研究。结果表明:南海近海海水中的总α、总β含量,略高于东海,稍低于渤海。南海近海海域的主要放射性物质是铀、钍天然放射系和~(40)K。     

Sulfur and iron speciation in surface sediments along the northwestern margin of the Black Sea

The speciation of sedimentary sulfur (pyrite, acid volatile sulfides (AVS), S⁰, H₂S, and sulfate) was analyzed in surface sediments recovered at different water depths from the northwestern margin of the Black Sea. Additionally, dissolved and dithionite-extractable iron were quantified, and the sulfur isotope ratios in pyrite were measured. Sulfur and iron cycling in surface sediments of the northwestern part of the Black Sea is largely influenced by (1) organic matter supply to the sediment, (2) availability of reactive iron compounds and (3) oxygen concentrations in the bottom waters. Biologically active, accumulating sediments just in front of the river deltas were characterized by high AVS contents and a fast depletion of sulfate concentration with depth, most likely due to high sulfate reduction rates (SRR). The δ³⁴S values of pyrite in these sediments were relatively heavy (−8‰ to −21‰ vs. V-CDT). On the central shelf, where benthic mineralization rates are lower, re-oxidation processes may become more important and result in pyrite extremely depleted in δ³⁴S (−39‰ to −46‰ vs. V-CDT). A high variability in δ³⁴S values of pyrite in sediments from the shelf-edge (−6‰ to −46‰ vs. V-CDT) reflects characteristic fluctuations in the oxygen concentrations of bottom waters or varying sediment accumulation rates. During periods of oxic conditions or low sediment accumulation rates, re-oxidation processes became important resulting in low AVS concentrations and light δ³⁴S values. Anoxic conditions in the bottom waters overlying shelf-edge sediments or periods of high accumulation rates are reflected in enhanced AVS contents and heavier sulfur isotope values. The sulfur and iron contents and the light and uniform pyrite isotopic composition (−37‰ to −39‰ vs. V-CDT) of sediments in the permanently anoxic deep sea (1494 m water depth) reflect the formation of pyrite in the upper part of the sulfidic water column and the anoxic surface sediment. The present study demonstrates that pyrite, which is extremely depleted in ³⁴S, can be found in the Black Sea surface sediments that are positioned both above and below the chemocline, despite differences in biogeochemical and microbial controlling factors.     

Seasonal and decadal shifts in particulate organic matter processing and sedimentation in the Bering Strait Shelf region

We present data on the quality and quantity of particulate organic material deposited to the benthos in the Chukchi Sea. This analysis is undertaken by using ⁷Be, a short-lived radiotracer, which is associated with particle deposition, the stable carbon isotopic composition of organic material and its C/N ratio in the water column and within the sediments, and the inventories of chlorophyll a present in surface sediments. Using previously published data, we show that sedimentation processes in the regional Bering Strait ecosystem may have shifted in the past decade. Surface sediments collected in 2004 adjacent to the Russian coastline in the Chukchi Sea are less refractory in terms of carbon isotope ratios and C/N ratios than was observed for surface sediments at similar locations in 1995 and 1988. Based upon sediment ⁷Be and chlorophyll a inventories, short-term sedimentation on the shelf occurs immediately north of Bering Strait, and within and downstream of Barrow and Herald Canyons. Seasonal differences (i.e., ice-covered versus open-water conditions) in the quality of particulate organic carbon reaching the benthos appear to be small in the most productive waters, such as Barrow Canyon. However, in less productive waters, C/N ratios and δ¹³C values show seasonal variations. Once on the bottom, δ¹³C values in the organic fractions of the sediments are less negative than observed in settling material in the water column, which is commonly thought to result from biological processing within the sediments.     

Temporal variability of Pb fluxes and bioturbation in shelf sediments beneath the high primary production area off Concepción, central-southern Chile (36°S)

We estimated monthly fluxes of ²¹⁰Pb in shelf sediments beneath a high productivity area off central-southern Chile (36°S) during 1 year (September 2002-August 2003). Sediment cores were obtained using a multiple corer and were analyzed mainly for ²¹⁰Pb, total pigments, and macrofauna abundance. The ²¹⁰Pb inventories and fluxes were estimated for surface sediments (0-5 cm) and bioturbation coefficients were inferred using chlorophyll-a (reactive) profiles. In general, ²¹⁰Pb content was inversely correlated with phytodetritus fluxes. High photosynthetic pigment contents in surface sediments were consistently associated with lower ²¹⁰Pb contents. Macrofaunal activity responded to oxygen and organic matter supplies at the sediment surface, generally concentrated in the first centimeters, but particularly so during months of high organic matter fluxes and deficient bottom water oxygen conditions. At this study site, several processes involved in the ²¹⁰Pb surface distribution make it difficult to accurately estimate ages at the surface. We postulate that the organic fluxes promote changes in the faunal activity, which, in combination with sediment resuspension and water circulation over the shelf, produce seasonal variations in the ²¹⁰Pb inventories.     

Variability of organic δC and C/N in the Mersey Estuary, U.K. and its implications for sea-level reconstruction studies

Microfossil analysis (e.g. diatoms, foraminifera and pollen) represents the cornerstone of Holocene relative sea-level (RSL) reconstruction because their distribution in the contemporary inter-tidal zone is principally controlled by ground elevation within the tidal frame. A combination of poor microfossil preservation and a limited range in the sediment record may severely restrict the accuracy of resulting RSL reconstructions. Organic δ¹³C and C/N analysis of inter-tidal sediments have shown some potential as coastal palaeoenvironmental proxies. Here we assess their viability for reconstructing RSL change by examining patterns of organic δ¹³C and C/N values in a modern estuarine environment. δ¹³C and C/N analysis of bulk organic inter-tidal sediments and vegetation, as well as suspended and bedload organic sediments of the Mersey Estuary, U.K., demonstrate that the two main sources of organic carbon to surface saltmarsh sediments (terrestrial vegetation and tidal-derived particulate organic matter) have distinctive δ¹³C and C/N signatures. The resulting relationship between ground elevation within the tidal frame and surface sediment δ¹³C and C/N is unaffected by decompositional changes. The potential of this technique for RSL reconstruction is demonstrated by the analysis of part of an early Holocene sediment core from the Mersey Estuary. Organic δ¹³C and C/N analysis is less time consuming than microfossil analysis and is likely to provide continuous records of RSL change.     

Faunal characteristics and sediment accumulation processes in the James River estuary,Virginia

This study was designed to relate fauna characteristics and sediment accumulation processes in the James River, VA and was conducted during June 1981. Physical sedimentary and benthic biological parameters, as well as sediment structure and radionuclide profiles, were evaluated for 11 stations. Faunal distribution patterns reflected species' response to salinity changes along the estuarine gradient, but not to differences in sediment accumulation rates. Levels of bioturbation could not be predicted easily on the basis of faunal characteristics alone. Results suggest that the physical processes of erosion and deposition strongly influence the ability of macrobenthos to bioturbate sediments in this estuary. Areas of rapid deposition (>3 cm y⁻¹) exhibit little evidence of bioturbation, as do areas where erosion, or relatively constant physical reworking of sediments, dominate. Areas with low sediment accumulation rates (0·5-3 cm y⁻¹) exhibit the highest levels of mixing as evidenced in X-radiographs. Estuarine organisms inhabiting soft bottoms are typically ‘opportunistic’, shallow-living and short-lived species, and the composition of their communities is not strongly influenced by rates of deposition. Physical reworking of sediments is most likely to occur near to the sediment-water interface where reworking by shallow-living organisms is most intense. Sediment-mixing processes should be characterized using a range of approaches. The phasing of interactions among erosion, physical transport, deposition and biological mixing must be resolved on the appropriate time scales if the mechanics of processes governing the formation of the sedimentary record are to be elucidated.