Sedimentary processes in the inner New York Bight: Evidence from excess210Pb and239,240Pu

Particle-reactive radionuclides were determined in sediments from the inner New York Bight to trace transport and storage of fine-grained sediments and associated reactive materials. Seven sediment ? cores 20–50 cm in length were analyzed for water content, loss on ignition (LOI) and excess²¹⁰Pb; three of these were also analyzed for^239,240Pu. Excepting some depth horizons in a core from a dredge-spoil dumpsite, every sample analyzed contained excess²¹⁰Pb. Variations in the concentration of excess²¹⁰Pb with depth in the sediment at all stations correlated strongly with LOI, which apparently traces that fraction of the sediment which is active in removing reactive elements from the water column. In the cores analyzed for^239,240Pu, every sample contained finite Pu, and Pu concentrations correlated strongly with excess²¹⁰Pb.The radionuclide distributions may be simply viewed as products of steady-state sediment accumulation or of mixing. Geochemically reasonable accumulation rates are very high (0.5–2.6 g/cm² y) and could probably only be sustained by offshore transport of dumped materials. At the other extreme the relationships between excess²¹⁰Pb and LOI are compatible with rapid mixing of a²¹⁰Pb carrier phase (traced by LOI) into the pre-existing substrate with little or no actual accumulation. Other non-steady-state processes, such as sediment gravity flow, could also explain the observed distributions.Measured sediment inventories (dpm/cm²) of excess²¹⁰Pb and Pu at these stations are greatly in excess of those supportable by direct atmospheric deposition: lateral supply is required. Incorporation of sedimentary fines into the sand substrate could make the inner New York Bight an important repository of reactive materials.     

Fine scale distributions of porosity and particulate excess210Pb,organic carbon and CaCO3 in surface sediments of the deep equatorial Pacific

Sediment samples were recovered from the central equatorial Pacific Ocean, sectioned at 1-mm intervals, and analyzed for porosity, organic carbon, excess²¹⁰Pb and CaCO₃. Steep porosity gradients were measured in the upper 1 cm of the sediment column with extremely high values observed near the sediment surface. Similarly, particulate organic carbon contents are highest at the sediment surface, decrease sharply in the upper 1 cm, and are relatively constant between 1 and 5 cm. CaCO₃ values, on the other hand, are lowest at the sediment surface and increase to a constant value below 5–10 mm depth. At the carbonate ooze sites, excess²¹⁰Pb is present throughout the upper 5 cm of the sediments suggesting relatively rapid particle mixing rates. However, extremely high excess²¹⁰Pb activities (> 100 dpm/g) are observed at the sediment surface with sharp gradients present in the upper 1 cm which would suggest slow rates of mixing. This apparent contradiction along with the major features of the CaCO₃ and particulate organic carbon profiles can be explained by a particle-selective feeding mechanism in which organic carbon, excess²¹⁰Pb-enriched particles are preferentially maintained at the sediment surface via ingestion and defecation by benthic organisms.     

Pu in coastal marine environments

Analysis of water samples from the New York Bight area and Narragansett Bay reveals that a small fraction of the total Pu (probably Pu (III + IV) species) is continuously removed to the sediments at a rate similar to that of the particle-reactive isotope²²⁸Th. A more “soluble” Pu species appears to be released at times from the sediments to the water column in these nearshore regions. Sediments in shallow areas of the New York Bight south of Rhode Island and Narragansett Bay have high Pu inventories and relatively deep penetration of this element, although the net sediment accumulation rate is generally low (<0.03 g/cm² yr). The high Pu inventories can be explained if both sediment resuspension and sediment mixing are assumed to be the major controlling factors for the effective transfer of Pu from the water column to the sediments. By simultaneous modelling of the depth distribution of three tracers which operate on vastly different time scales:²³⁴Th (half-life 24 days),²¹⁰Pb (half-life 22 years) and^239,240Pu (introduced into the environment during the past 30 years), bioturbation rates ranging from 4 to 32 cm²/yr in the surface mixed layer (5–10 cm thick) and from 0.3 to 2.5 cm²/yr in the layer below (up to 40 cm thick) and net sediment accumulation rates of approximately zero to 0.14 g/cm² yr were calculated for these areas.     

Fine scale distributions of porosity and particulate excessPb, organic carbon and CaCO3 in surface sediments of the deep equatorial Pacific

Sediment samples were recovered from the central equatorial Pacific Ocean, sectioned at 1-mm intervals, and analyzed for porosity, organic carbon, excess²¹⁰Pb and CaCO₃. Steep porosity gradients were measured in the upper 1 cm of the sediment column with extremely high values observed near the sediment surface. Similarly, particulate organic carbon contents are highest at the sediment surface, decrease sharply in the upper 1 cm, and are relatively constant between 1 and 5 cm. CaCO₃ values, on the other hand, are lowest at the sediment surface and increase to a constant value below 5–10 mm depth. At the carbonate ooze sites, excess²¹⁰Pb is present throughout the upper 5 cm of the sediments suggesting relatively rapid particle mixing rates. However, extremely high excess²¹⁰Pb activities (> 100 dpm/g) are observed at the sediment surface with sharp gradients present in the upper 1 cm which would suggest slow rates of mixing. This apparent contradiction along with the major features of the CaCO₃ and particulate organic carbon profiles can be explained by a particle-selective feeding mechanism in which organic carbon, excess²¹⁰Pb-enriched particles are preferentially maintained at the sediment surface via ingestion and defecation by benthic organisms.     

Atmospherically-derived radionuclides as tracers of sediment mixing and accumulation in near-shore marine and lake sediments: Evidence from7Be,210Pb,and239,240Pu

Cosmogenic⁷Be(t_1/2 = 53.3days) has been used to estimate particle-mixing rates in the upper layers of lacustrine and near-shore marine sediments. Excess²¹⁰Pb and/or^239,240Pu have provided limits on rates of sediment accumulation in these environments and indices of the efficiency of the sediments as collectors of reactive nuclides over longer time scale.In sediment cores from Long Island Sound (marine) and Lake Whitney (fresh-water)⁷Be was measurable in the top 2–3 cm. Diffusion-analog particle-mixing coefficients calculated from these data are in the range of 10^?7 cm²/s. For Long Island Sound the coefficients are lower by factors of 3–6 than those estimated from the depth distributions of excess²³⁴Th at the same stations [14]. For Lake Whitney the calculated mixing coefficient is an upper limit because of the possibility of a sampling artifact.Measurements of total (wet + dry) atmospheric deposition of⁷Be in New Haven give an average flux of 0.07 dpm/cm² day during March-November, 1977; this is equivalent to a steady-state inventory of 5.4 dpm/cm² in a perfect collector. Sediment cores from Long Island Sound contain about half this⁷Be inventory, consistent with either a mean residence time for⁷Be in the water column of about one half-life or with post-depositional loss of⁷Be from Long Island Sound sediments. The Lake Whitney cores contain about 5 dpm/cm², much nearer the atmospheric delivery. A higher inventory of⁷Be in fresh-water, as compared to marine, sediments could be due either to a shorter mean residence time for⁷Be in fresh water or to lateral transport processes in the lake or its catchment. High inventories of excess²¹⁰Pb and^239,240Pu in Lake Whitney sediments demonstrate the importance of lateral transport on longer time scales at least.     

Dating of sediments from Lake Zurich (Switzerland) with210Pb and137Cs

²¹⁰Pb- and¹³⁷Cs-measurements, and varve counting have been used to date sediment cores from Lake Zurich (Switzerland). Two cores from different water depths were dated with²¹⁰Pb/²¹⁰Po and revealed sediment accumulation rates of (0.055±0.015) g·cm^?2·y^?1 and (0.09±0.03) g·cm^?2·y^?1, respectively. A comparable rate of (0.07±0.01) g·cm^?2·y^?1 has been obtained from¹³⁷Cs measurements. These rates were confirmed by annual layer (varve)-counts which lead to rates of 0.07 g·cm^?2·y^?1. Constant²¹⁰Pb activities were observed in the top 6 cm of the sediment cores. This constancy is generally explained in the literature by mixing processes caused by bioturbation and by distortion during coring operations of the uppermost water-rich fluffy sediments. However the distinct¹³⁷Cs-maxima and the regular and undisturbed varve lamination of the top sediment observed in the cores of Lake Zurich contradict this assumption. In addition, measurements of⁷Be at the water/sediment interaces proved complete sediment core recovery and mechanically undisturbed sediments. Remobilization processes are assumed to cause the observed constant²¹⁰Pb activities. Remobilization may also be the reason for an incomplete²¹⁰Pb inventory in the sediments which contain only about 50% of the fallout from atmosphere. The results of the²¹⁰Pb dating should therefore be considered with some care. If existent, varve counting represents the easiest and most reliable means for dating lake sediments.     

Plutonium and210Pb distributions in northeast Atlantic sediments: subsurface anomalies caused by non-local mixing

The depth distributions of²¹⁰Pb and^239,240Pu measured in a suite of box cores collected from water depths of 4000–5000 m in the northeast Atlantic Ocean exhibit pronounced subsurface maxima caused by sediment reworking by benthic infauna. Small-scale spatial heterogeneity in bioturbation rates is indicated by large differences in tracer profiles from duplicate cores separated only by a few centimeters.²¹⁰Pb and^239,240Pu activity distributions from each subcore exhibit a high degree of correlation, and most tracer profiles exhibit one or more subsurface maxima.One-dimensional, “biodiffusion” analogue models do not adequately simulate the principal features of this data set. However, an inverse “conveyer belt” mixing model which simulates subsurface egestion (or a functionally equivalent process) of surficial material which is enriched both in organic debris and radioactive tracers can reproduce the subsurface tracer maxima. Single-event and continuous subsurface egestion models have been formulated and solved for different “feeding rates” and background biodiffusive fields. The single-event model provides a better fit to the data and, in particular, ensures the observed, high degree of correlation between the²¹⁰Pb and^239,240Pu activity profiles, regardless of the different tracer input functions. The most likely candidate responsible for subsurface tracer egestion is a large infaunal worm of the phylum Sipunculida which dominates the biomass below a depth of 3 cm.     

Southern California inner basin sediment trap calibration

The deployment of particle interceptor traps (PITs) in the three inner basins of the Southern California Bight (Santa Barbara, Santa Monica, and San Pedro) where preserved, laminated, bottom sediments occur, provides a natural calibration between the parameters determined with the PITs and those derived from the historical sedimentary deposits. The accumulation rates and chemical composition of the PIT materials compare favorably with these recently deposited bottom sediments. The ratio of the measured particle collection rate to the sediment accumulation rate for these three basins averaged0.93±0.20. Radionuclide (²¹⁰Pb,²²⁸Th/²³²Th) and trace element (Fe, Cu, Zn, Cd, Pb) compositions of the PIT materials and surface sediments agree within, generally, 30% in each basin.An application of PITs as a sampling system in an outer basin (San Nicolas) where the sedimentary record has been obscured by bioturbation is also presented to further demonstrate the utility of PITs for spatial and temporal studies of various aspects of particle transport and sediment deposition. Based on the calibration of the PITs in the three inner basins we conclude from the comparison of the radionuclide and trace element compositions between the PIT materials and surface sediments from the San Nicolas Basin that recently deposited sedimentary material has been mixed by bioturbation with older material from the last several hundred years. Excess²¹⁰Pb and the²²⁸Th/²³²Th activity ratio in the PIT material are 6 and 15 times higher than in the surface sediment. Total Pb and1N HNO₃-leachable Pb are 4- and 8-fold higher in the PIT material.     

230Th,226Ra and222Rn in abyssal sediments

A model that predicts the flux of²²²Rn out of deep-sea sediment is presented. The radon is ultimately generated by²³⁰Th which is stripped from the overlying water into the sediment. Data from many authors are compared with the model predictions. It is shown that the continental contribution of ionium is not significant, and that at low sedimentation rates, biological mixing and erosional processes strongly affect the surface concentration of the ionium. Two cores from areas of slow sediment accumulation, one from a manganese nodule region of the central Pacific and one from the Rio Grande Rise in the Atlantic were analyzed at closely spaced intervals for²³⁰Th,²²⁶Ra, and²¹⁰Pb. The Pacific core displayed evidence of biological mixing down to 12 cm and had a sedimentation rate of only 0.04 cm/kyr. The Atlantic core seemed to be mixed to 8 cm and had a sedimentation rate of 0.07 cm/kyr. Both cores had less total excess²³⁰Th than predicted.Radium sediment profiles are generated from the²³⁰Th model. Adsorbed, dissolved, and solid-phase radium is considered. According to the model, diffusional losses of radium are especially important at low sedimentation rates. Any particulate, or excess radium input is ignored in this model. The model fits the two analyzed cores if the fraction of total radium available for adsorption-desorption is about 0.5–0.7, and ifK, the distribution coefficient, is about 1000.Finally, the flux of radon out of the sediments is derived from the model-generated radium profiles. It is shown that the resulting standing crop of²²²Rn in the overlying water may be considered as an added constraint in budgeting²³⁰Th and²²⁶Ra in deep-sea sediments.     

The half life of32Si determined from a varved Gulf of California sediment core

Excess²¹⁰Pb measurements and varve chronology were used to establish a sediment accumulation rate of 0.19 cm/yr in a 95-cm-long box core raised from the Gulf of California. Varve thickness is unchanged over the entire length of the core, indicating a constant rate of sediment accumulation. The³²Si specific activity of biogenic silica shows an exponential decrease with depth in this core. The half life of³²Si, calculated from these data and the 0.19-cm/yr sediment accumulation rate, is276 ± 32 years. As most of the silica and³²Si supplied to the Gulf of California is a result of upwelling of deep ocean water, this half life determination should be relatively insensitive to secular variations in the atmospheric supply of³²Si.     

Radioactivity in sediments of the Great Lakes: Post-depositional redistribution by deposit-feeding organisms

At two locations in southern Lake Huron (U.S.A.), twelve 35.5-cm diameter cores of fine-grained sediments were taken for comparison of the vertical distributions of²¹⁰Pb and falllout¹³⁷Cs with the distributions of benthic macroinvertebrates, mainly oligochaete worms (Tubificidae) and the amphipod,Pontoporeia affinis. Locations were selected on the basis of²¹⁰Pb distributions measured a year earlier which indicated contrasting depths of mixing of surface sediments. At one location the activity of²¹⁰Pb is uniform down to about 6 cm and 95% of total invertebrates occur within this zone; at the other location the zone of constant activity is only 3 cm deep but 90% of the invertebrates occur within it. Comparison of published tubificid defecation rates with sediment accumulation rates based on²¹⁰Pb shows that oligochaetes alone can account for mixing in one case while the effects of amphipods may be required in the case of shallower mixing. If mixing is represented as a diffusional process, eddy diffusion coefficients are at least 5.8 and 3.3 cm² yr^?1 at respective locations. In comparison with bioturbation, molecular diffusion is of minor importance in the post-depositional mobility of¹³⁷Cs. The necessity for introducing a diffusion coefficient varying continuously with depth is indicated by characteristics of the distribution of¹³⁷Cs. Biological reworking of near-surface sediments is an important process affecting radioactivity and chemical profiles in profundal deposits of this and probably other Great Lakes.     

Decadal record of sediment export to the deep sea via Eel Canyon

An active upper-canyon system, Eel Canyon, was studied to determine its role as a conduit and/or sink for terrigenous material over decadal timescales and to assess the sedimentary record preserved by transport processes. These data are used to (1) link seasonal fluctuations in sediment transport and deposition to preserved stratigraphic signatures, and (2) assess sediment storage and removal in the upper Eel Canyon (100–850 m water depth) over decadal timescales. Previous research has shown that upper thalwegs commonly experience gravity-driven flows during winter (November–March), due to increased sediment supply from Eel River flooding and intense storms that produce energetic wave/current conditions. Thick winter deposits composed of recently discharged fluvial sediment are formed in upper thalwegs, with distinct short- and long-lived radioisotopic and textural signatures (detectable ⁷Be and ²³⁴Th_xs, lowered ²¹⁰Pb activity, elevated clay content, and physical structures). Box and kasten cores were collected in the upper canyon (thalwegs and walls) to measure these signatures in recent and preserved winter deposits, and to calculate 100-yr accumulation rates. Non-bioturbated deposits (that have signatures indicative of rapid accretion by gravity-driven flows during the winter) are common in the upper canyon thalwegs. Short-lived radioisotopes (⁷Be and ²³⁴Th) show that sediment delivery to the upper thalweg varies temporally, sometimes beginning at the onset of river flooding, and at other times beginning during fall/early winter dry-storm events. In contrast, bioturbated deposits (which do not have signatures indicative of rapid deposition) are found on canyon walls.Non-bioturbated winter deposits are easily identified in the decadal record of thalwegs by decreases in ²¹⁰Pb activity and increases in clay content. Stacking of multiple years of winter deposits (∼10 cm preserved per winter) results in non-steady-state ²¹⁰Pb profiles and high decadal accumulation rates. However, down-core changes in ²¹⁰Pb profiles show that slope failures are actively redistributing these winter deposits. Partial or total removal of multiple winter deposits appears to happen periodically (every ∼13 yr), which will inhibit preservation of the longer decadal record. 100-yr accumulation rates were calculated in the thalwegs from the resulting ²¹⁰Pb profiles (i.e., the result of winter accretion and decadal removal by failures). Accumulation rates are much higher in thalwegs (1–6 cm/yr) than walls (0.1–0.8 cm/yr), which is likely the result of differing sediment delivery processes (via gravity-driven flows and nepheloid layers, respectively). At least 2.6±1.4% of the Eel River sediment budget is accumulating in the upper canyon over 100-yr timescales. However, this value greatly underestimates the total amount entering the canyon system because minimum accumulation rates were used in many areas (due to limited core length) and slope failures are moving sediment out of the budget area.     

Chemical composition of short sediment cores from Thermaikos Gulf (Eastern Mediterranean): Sediment accumulation rates, trawling and winnowing effects

Four cores recovered within the framework of the INTERPOL Project have been analysed for their grain size and geochemistry; sediment accumulation rates (SARs) were also determined from ²¹⁰Pb and ¹³⁷Cs profiles. Two cores are representative of the Axios and Aliakmon Rivers depositional environment, whilst the third core represents the Pinios River province; the fourth core represents an environment of outer shelf relict sands. Apparent SARs ranged between 0.667 g cm⁻² yr⁻¹ (Axios and Aliakmon Rivers) and 0.414 g cm⁻² yr⁻¹ (Pinios River). Trawling activities and biomixing are critical processes that may be responsible for the mixing of the surface sediments, as observed from the excess ²¹⁰Pb profiles. The thickness of the surface mixed layer was 4.5 cm in the vicinity of Axios and Aliakmon Rivers and in the area of Pinios River, 3.75 cm on the outer shelf and 1 cm in the area where no trawling was observed. Sediment accumulation appeared to be regulated by variations in the riverine discharge, shelf transport pathways and winnowing processes. Major element variations, such as Si, Al, Ti, V and Ni, were dominated by terrigenous supply as aluminosilicate minerals and quartz, whereas most Ca and Sr were biogenic. Si/Al and Ca/Al ratios have been used to express changes in sediment accumulation and winnowing. Redox processes were depicted by Mn, which showed an increase in the depth of its redoxcline, from 1 cm in inshore stations to 2 cm on the outer shelf. Si/Al ratios follow the Ca/Al ratios and can be used to assess percentage winnowing in the sediment. Increases in these ratios indicate a decrease in sediment input rates and are seen in the upper parts of most of the cores. Anthropogenic or ‘excess’ metal contents have been calculated from Zn/V and Pb/V ratios. Their distributions in the cores showed that by far the highest contamination is associated with the Axios River output, whilst sediments influenced by the Pinios River were relatively uncontaminated.     

226Ra chronology of a coastal marine sediment

Unsupported²²⁶Ra (t₁₂ = 1620years) in marine sediments can provide a basis for measuring rates of accumulation of the order of centimeters per thousand years. The excess radium apparently enters the sediments incorporated in phytoplankton. The sensitivity of the method depends upon the initial value of the unsupported²²⁶Ra and of the value of²³⁰Th, a parent of²²⁶Ra, in the sedimentary components.²²⁶Ra dating was applied to a sediment taken from the slope of the San Clemente Basin in the Southern California coastal region. Rates of sedimentation over two half-lives of the nuclide were found to be either 5.2 or 5.3 cm/1000 years depending upon which of two models for the geochronology is used. One model assumes that the²³⁰Th brings to the deposit an amount of²²⁶Ra in equilibrium with it. The other is based upon the growth of the²²⁶Ra from the²³⁰Th in the sedimentary components.^238+239Pu and²¹⁰Pb levels in the upper strata indicated sedimentation rates of the order of 100–500 cm/1000 years, i.e. much faster accumulations. We suggest these derived rates are spurious and reflect bioturbative activities of surface-living organisms.     

The coagulation of dissolved239, 240Pu in estuaries as determined from a mixing experiment

A mixing experiment, using large volumes (100 l) of filtered (< 1 μm) freshwater and seawater end-members, was performed to simulate and investigate the chemical reactivity of^{239, 240}Pu during estuarine mixing. An organic-rich freshwater with a relatively high concentration (0.8 dpm/100 l) of dissolved^{239, 240}Pu was used as one end-member; Buzzards Bay seawater (dissolved^{239, 240}Pu= 0.04dpm/100l) was the other. The results demonstrate that dissolved^{239, 240}Pu in the freshwater undergoes extensive and rapid coagulation under simulated estuarine conditions. There is a strong correlation between the amount of coagulation of dissolved^{239, 240}Pu, humic acids (HA), and Fe. The extent of coagulation of all three constituents increases with increasing salinity and the net extent of their removal is 53%, 57%, and 100% for Pu, HA, and Fe respectively. As has been documented for Fe in freshwater, dissolved^{239, 240}Pu appears to be stabilized by naturally occurring humic substances to form negatively charged colloids which are then coagulated by seawater cations. The extrapolation of these experimental results to real estuaries will require additional research.     

Recent aquatic ecosystem response to environmental events revealed from Pb sediment profiles

The ²¹⁰Pb dating method was first introduced by Goldberg (1963), and since then has been applied to study sediment from lakes, estuaries and coastal marine environments. Hundreds of studies around the world have used ²¹⁰Pb as a geochronological tool in aquatic ecosystems. However little attention has been paid to the potential of this naturally occurring isotope as an environmental tracer of ecological events. Here we report three instances in which ²¹⁰Pb profiles measured on undisturbed sediment cores from lakes, rivers and fjords show us the potential of ²¹⁰Pb profile as a tracer of natural and anthropogenic processes. The methodology used here is a suite of techniques combining biogeochemistry (micro-electrodes), paleomagnetism (susceptibility), sediment characteristics (LOI) and visualization (SPI and X-ray) applied to the interpretation of ²¹⁰Pb profiles. We measured ²¹⁰Pb profiles on sediments from a river, Cruces River (Chile), which recorded a clear shift in the water chemistry caused by a pulp mill effluent to the river. Here metal mobilization and remobilization of the tracer may be the cause of the observed profile. We also measured ²¹⁰Pb profiles in sediment from two fjords of Southern Chile (Pillan and Reñihue), the sudden deposition change of fresh ²¹⁰Pb with depth observed could very well be the result of bioturbation but it occurred in a seafloor area deprived of bioturbators. In this case, ²¹⁰Pb recorded the onset of aquaculture activities (fish farming) that took place two decades ago. Finally, ²¹⁰Pb profiles measured in two lakes in the “pampa Argentina”: Epecuen and Venado showed a particular shape with depth. These profiles apparently registered a sudden depositional event with recent ²¹⁰Pb material, probably related to strong shifts in precipitation and drought cycles in that part of the world. These three examples show that ²¹⁰Pb profiles provide valuable information not only on geochronology, but also related to natural and anthropogenic short term processes, as shown here, but these are not always reported and well understood.     

A quantitative examination of modern sedimentary lithofacies formation on the glacially influenced Gulf of Alaska continental shelf

Continental-shelf lithofacies are described from a series of cores collected in the northern Gulf of Alaska, a high-energy paraglacial shelf experiencing rapid rates of sediment accumulation. Short-lived tracers (²³⁴Th and chlorophyll-a) indicate that during the annual peak in fluvial sediment input (summer), biologic sediment mixing coefficients in the surficial seabed are generally lower than other coastal environments (<20 cm² yr⁻¹) and mixing extends downward <10 cm.²¹⁰Pb geochronology indicates that sediment accumulation rates (time scales of 10–100 yr) are 0.1–3 cm yr⁻¹. The measured bioturbation and accumulation rates lead to predictions of moderate to bioturbated lithofacies, as observed. Primary depositional fabric is preferentially preserved where sediment accumulation rates >2 cm yr⁻¹ and non-steady sediment deposition occurs. Depositional fabric is also observed in strata at 50–100 m water depths and is similar in appearance to beds that may form through deposition of wave-induced fluid-mud flows, which have been observed forming on other shelves with moderate to high wave energy. Five general lithofacies can be identified for the study area: inner-shelf sand facies, interbedded sandy mud facies, moderate-to-well-bioturbated mud facies, gravelly mud facies, and Tertiary bedrock facies. The moderate-to-well-bioturbated mud facies is areally dominant, representing over 50% of the shelf area, although roughly equal volumes (∼0.4 km³) of strata with some preservation of primary fabric are annually accumulating. Lithofacies on this paraglacial shelf generally resemble mid- and low-latitude allochthonous shelf strata to a much greater degree than Holocene glacimarine strata formed on shelves dominated by icebergs and floating ice shelves. Paraglacial strata may be differentiated from non-glacial shelf strata by lower organic carbon concentrations, a relatively lower degree of bioturbation, and increased preservation of primary depositional fabric.     

Sorption of radioactive contaminants by sediment from the Kara Sea

The purpose of this study is to quantify some of the parameters needed to perform near-field modelling of sites in the Kara Sea that were impacted by the disposal of radioactive waste. The parameters of interest are: the distribution coefficients (Kd) for several important radionuclides, the mineralogy of the sediment, and the relationship of Kd to liquid-to-solid ratio. Sediment from the Kara Sea (location: 73 degrees 00'N, 58 degrees 00'E) was sampled from a depth of 287 m on August 23/24, 1992. Analysis of the material included mineralogy, grain size and total organic carbon (TOC). Uptake kinetics were determined for 85Sr, 137Cs, 241Am, 99Tc, 1251, 232U and 210Pb and distribution coefficients (Kd) were determined for these radionuclides using batch type experiments. Sorption isotherms, developed for 137Cs, 85Sr and 99Tc, were linear in each case. Increasing the liquid-to-solid ratio strongly increased uptake of 137Cs and moderately increased uptake of 99Tc. Analysis for anthropogenic radionuclides indicated the presence only of 239/240Pu in the sediment with the highest activity (at the top section of the core) being 0.420 Bq kg(-1). Other anthropogenic radionuclides were below detection limits.     

Estimates of particle flux and reworking at the deep-sea floor using234Th/238U disequilibrium

Because of high specific activities of excess²³⁴Th (t_1/2 = 24.1 days) on suspended particles in the deep sea, this nuclide is potentially an extremely sensitive indicator of particle inputs and dynamics at the seafloor. Measurements were made at two deep-sea sites in order to examine this potential. Inventories of excess²³⁴Th at a low-current hemipelagic mud site (3990 m) in the Panama Basin were～ 1.5 (September, ′81) and～ 2.5 (June, ′82) dpm/cm². The steady state fluxes to the seafloor calculated from these inventories are in rough agreement with radionuclide fluxes measured in sediment traps. Small-scale (～ 100m) spatial variability in inventories implies biologically significant heterogeneity in particle inputs. Sediment from the continental rise site in the northwest Atlantic (2800 m), a site with higher current velocities than the Panama Basin, had an inventory of～ 1.9dpm/cm². This inventory is also in rough agreement with predictions made on the basis of nearby sediment trap data. Particle mixing coefficients of～ 30cm²/yr calculated at the Pacific and Atlantic sites are similar to those in shallow water deposits but could reflect disturbance during handling. Based on²¹⁰Pb data from the Panama Basin, sediment from below～ 6cm is mixed at a rate～ 10 × slower than the near-surface sediment to a depth of at least 20 cm. Agreement between²³⁴Th predicted mixing rates at the Panama Basin site with²¹⁰Pb profiles and in-situ experiments with glass bead tracers implies that these rates are real. Although the diffusion of dissolved²³⁴Th into deep-sea sediments complicates interpretations,²³⁴Th_xs distributions in bottom sediments offer a useful adjunct to sediment traps for investigation of particle dynamics near the deep-sea floor.