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1.
Cosmogenic7Be(t1/2 = 53.3days) has been used to estimate particle-mixing rates in the upper layers of lacustrine and near-shore marine sediments. Excess210Pb and/or239,240Pu 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 and239,240Pu in Lake Whitney sediments demonstrate the importance of lateral transport on longer time scales at least.  相似文献   

2.
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) and239,240Pu (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.  相似文献   

3.
An experiment was designed to assess the relative importance of sediment accumulation and bioturbation in determining the vertical distribution of nuclides in estuarine sediments. A diver-collected core, 120 cm long, was raised from central Long Island Sound and analyzed down its length for:210Pb and226Ra;239, 240Pu; and Mn, Zn, Cu, and Pb. Sampling for chemical analysis was guided by X-radiography of the core. Excess210Pb (relative to226Ra) is roughly homogeneous in the top 2–4 cm of the core, then decreases quasi-exponentially to zero at (or above) 15 cm.239, 240Pu and excess Zn, Cu, and Pb, relative to background values at greater depths in the core, are distributed like excess210Pb in the top 10–15 cm. The absence of Mn enrichment at the top of the core, in contrast to other cores raised from this station, suggests that 1–3 cm of sediment was lost by erosion at the site of this core sometime prior to sampling. Below 15 cm excess210Pb and excess Zn, Cu, and Pb are found only in the bulk sample from 25 to 30 cm and in clearly identifiable burrow fillings dissected from 70 cm and 115 cm depth. Infilling of large burrows, excavated and then abandoned by crustaceans, is therefore a mechanism for transfer of surficial material to depth in these sediments.The bioturbation rate in the top several centimeters at this station has been determined previously using234Th (24-day half-life). The distribution of239, 240Pu can be used to estimate a bioturbation rate for the underlying layer (to ～10 cm depth); this rate is found to be 1–3% of the maximum mixing rate for the top 2–3 cm. Using these two mixing rates in a composite-layer, mixing + sedimentation model, the distribution of excess210Pb in the top 15 cm was used to constrain the sediment accumulation rate, ω. While the apparent rate of sediment accumulation (assuming no mixing below 2–4 cm) is 0.11 cm/yr, the model requires ω < 0.05 cm/yr. Thus in an area of slow sediment accumulation, a low rate of bioturbation below the surficial zone of rapid mixing causes an increase of at least a factor of two in apparent accumulation rate.  相似文献   

4.
Analyses are presented of137Cs,238Pu, and239,240Pu, in relation to depth in sediment, in 21 gravity cores. These cores span the ranges of times 1964–1975, and of water depths 12–2000 m; they come from three distinct sedimentation areas off the northeast coast of the United States. Although the ranges of total sediment inventories of239,240Pu and of137Cs from the various areas hardly overlap, the range of ratios of the inventories of these two nuclides is probably the same in all the areas. In the shallow-water cores the239,240Pu/137Cs ratio regularly diminishes with depth in the core, and a tendency is seen for curves of this function to have similar slopes in each area; ratios of238Pu/239,240Pu show no change with depth in these shallow-water cores. In the deeper-water cores, the239,240Pu/137Cs ratio shows no systematic change with depth, but sometimes the238Pu/239,240Pu ratio shows a minimum at the sediment surface, and is much higher deeper in the cores. We believe that these phenomena can be explained in terms of a complicated bioturbational process moving the nuclides, together, down into the sediments, of chemical resolubilization, at depth, of plutonium only, and of its subsequent upward translocation in the interstitial solution. Some re-immobilization of plutonium near the sediment surface is implied, and a mechanism is suggested for this, based on displacement of plutonium from organic complexes by the increasing concentrations, in upper layers of the sediment, of re-oxidized dissolved iron.  相似文献   

5.
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.  相似文献   

6.
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.  相似文献   

7.
The depth distributions of210Pb and239,240Pu 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 and239,240Pu 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 and239,240Pu 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.  相似文献   

8.
210Pb measurements were carried out on the sediments cores from a small south Belgian pond. In two cores, the210Pb activity decreases exponentially with depth. Under various assumptions described in the article, the corresponding accumulation rates would be of the order of 60–100 mg/cm2 of dried sediment per year.The stable lead content greatly increases from the older to the more recent sediment. This increase is accompanied by a change in isotopic composition: from the bottom to the top of the cores, the lead isotopic composition becomes progressively less radiogenic, reaching at the surface values identical to that for present atmospheric lead.  相似文献   

9.
The vertical distributions of210Pb and226Ra in the Santa Barbara Basin have been measured. The210Pb/226Ra activity ratio is close to unity in surface water, but ranges from 0.2 to 0.6 in deep water with a mean value of 0.3 (d > 250m), suggesting rapid removal of210Pb from the water column. The210Pb concentrations in the particulate phase at different water depths indicate that the removal of210Pb is due to adsorption on settling particles.It is estimated that the particulate210Pb contributes about 50–70% of the total210Pb measured on unfiltered water samples of the Santa Barbara Basin. The fate of210Pb (and Pb) in the water column is thus strongly controlled by the settling particles, which have a mean residence time of one year or less in the basin. Material balance calculation for210Pb in the basin suggests that there is an external source supplying about 70–80% of the210Pb observed in particulate material or sediments. This excess210Pb is most likely provided by particles entering the basin loaded already with210Pb.  相似文献   

10.
The distribution of210Po and210Po in dissolved (<0.4 μm) and particulate (>0.4 μm) phases has been measured at ten stations in the tropical and eastern North Atlantic and at two stations in the Pacific. Both radionuclides occur principally in the dissolved phase. Unsupported210Pb activities, maintained by flux from the atmosphere, are present in the surface mixed layer and penetrate into the thermocline to depths of about 500 m. Dissolved210Po is ordinarily present in the mixed layer at less than equilibrium concentrations, suggesting rapid biological removal of this nuclide. Particulate matter is enriched in210Po, with210Po/210Pb activity ratios greater than 1.0, similar to those reported for phytoplankton. Box-model calculations yield a 2.5-year residence time for210Pb and a 0.6-year residence time for210Po in the mixed layer. These residence times are considerably longer than the time calculated for turnover of particles in the mixed layer (about 0.1 year). At depths of 100–300 m,210Po maxima occur and unsupported210Po is frequently present. Calculations indicate that at least 50% of the210Po removed from the mixed layer is recycled within the thermocline. Similar calculations for210Pb suggest much lower recycling efficiencies.Comparison of the210Pb distribution with the reported distribution of226Ra at nearby GEOSECS stations has confirmed the widespread existence of a210Pb/226Ra disequilibrium in the deep sea. Vertical profiles of particulate210Pb were used to test the hypothesis that210Pb is removed from deep water by in-situ scavenging. With the exception of one profile taken near the Mid-Atlantic Ridge, significant vertical gradients in particulate210Pb concentration were not observed, and it is necessary to invoke exceptionally high particle sinking velocities to account for the inferred210Pb flux. It is proposed instead that an additional sink for210Pb in the deep sea must be sought. Estimates of the dissolved210Pb/226Ra activity ratio at depths greater than 1000 m range from 0.2 to 0.8 and reveal a systematic increase, in both vertical and horizontal directions, with increasing distance from the sea floor. This observation implies rapid scavenging of210Pb at the sediment-water interface and is consistent with a horizontal eddy diffusivity of 3?6 × 107 cm2/sec. The more reactive element Po, on the other hand, shows evidence of rapid in-situ scavenging. In filtered seawater,210Po is deficient, on the average, by ca. 10% relative to210Pb; a corresponding enrichment is found in the particulate phase. Total inventories of210Pb and210Po over the entire water column, however, show no significant departure from secular equilibrium.  相似文献   

11.
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.  相似文献   

12.
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.  相似文献   

13.
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.  相似文献   

14.
Because of high specific activities of excess234Th (t1/2 = 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,234Thxs distributions in bottom sediments offer a useful adjunct to sediment traps for investigation of particle dynamics near the deep-sea floor.  相似文献   

15.
Two ocean profiles from the Peru Basin from regions with different surface productivities were analyzed for total210Pb and201Po to evaluate the influence of particulates in the water column on their distribution. Comparison with a published226Ra profile for the region was made. The profile closest to the coast, where upwelling and productivity are high, shows depletion of210Pb relative to226Ra at all depths, with particularly marked excursions from radioactive equilibrium at the surface and in the bottom water.210Po appears to be deficient relative to210Pb at depth as well. Mean residence times in the deep water, relative to particulate removal from the water column to the sediments, of about 100 years for210Pb and about two years for210Po are indicated. The profile northwest of the upwelling region shows the226Ra210Pb210Po system close to equilibrium at all depths to 1500 m (except for the effect of atmospheric210Pb input seen at the surface.  相似文献   

16.
A large number of sediment cores collected during 2005-2010 from the Taiwan Strait were analyzed for radionuclides (210Pb, 137Cs and 7Be) to elucidate sedimentation dynamics in this all-important gateway linking two largest marginal seas in the western Pacific (namely, the South China Sea and the East China Sea). Apparent sediment accumulation rates derived from 210Pb and 137Cs profiles vary from <0.1 to >2 cm/yr, averaging ∼0.4 cm/yr and showing a spatial pattern closely related to hydrodynamics and sediment source-to-sink pathways. Spatial-temporal variation of 7Be activity in surface sediments off Taiwan’s west coast indicates episodic deposition of flood layers and their mobility from river estuaries toward the north. In conjunction with particle size distribution in surface sediments and the structure of sediment strata revealed by sub-bottom echo images; the radionuclide data can be used to outline three different sediment source-to-sink dispersal systems. Based on sediment loads of surrounding rivers and the distribution of sediment accumulation rates, lateral transport is required to account for the budget and size distribution of sediments in the strait.  相似文献   

17.
Anthropogenic radionuclides have reached the Hudson estuary as global fallout from nuclear weapons testing and through local releases from commercial nuclear reactors. Significant activities of238Pu and239,240Pu (fallout-derived),134Cs and60Co (reactor-released), and137Cs (derived from both sources), have accumulated in the sediments throughout the estuary, with the primary zone of accumulation near the downstream end of the system in New York harbor. The estuary appears to have trapped nearly all of the239,240Pu delivered as fallout, and consequently, ocean dumping of dredged harbor sediment is currently the primary means for the net transport of these nuclides to coastal waters. In contrast, only 10–30% of the137Cs,134Cs and60Co delivered to the estuary have been retained on the fine particles which accumulate at a rapid rate in the harbor.The primary factors which have governed the distribution of anthropogenic radionuclides in Hudson sediments are: (1) spread of fine particles labeled with both fallout and reactor nuclides throughout the axis of the estuary, (2) differences in timing of the peak fallout years (1962–1964) and years of maximum reactor releases (1971–1972), (3) large variations in sediment accumulation rates, ranging from a few millimeters per year or less to many tens of centimeters per year, (4) appreciable desorption of137Cs and134Cs from particles at higher salinities, and (5) possible enhanced desorption of60Co at higher salinities (relative to134Cs and137Cs) which may be associated with the release of reduced manganese from the harbor sediments.  相似文献   

18.
Particulate and soluble,210Pb activities have been measured by filtration of large-volume water samples at two stations in the South Atlantic. Particulate phase210Pb (caught by a 0.4-μm filter) varies from 0.3% of total210Pb in equatorial surface water to 15% in the bottom water. The “absolute activity” of210Pb per unit mass of particulate matter is about 107 times the activity of soluble210Pb per unit mass of water, but because the mass ratio of particulate matter to water is about 10?8, the particulate phase carries only about 10% of the total activity. In Antarctic surface water the particulate phase carries 40% of the total210Pb activity; the absolute activity of this material is about the same as in other water masses and the higher fraction is due to the much larger concentration of suspended matter in surface water in this region.In the equatorial Atlantic the particulate phase210Pb activity increases with depth, by a factor of 40 from surface to bottom, and by a factor of 4 from the Antarctic Intermediate Water core to the Antarctic Bottom Water. This increase with depth is predicted by our previously proposed particulate scavenging model which indicated a scavenging residence time of 50 years for210Pb in the deep sea. A scavenging experiment showed that red clay sediment removes all the210Pb from seawater in less than a week. The Antarctic particulate profile shows little or no evidence of scavenging in this region, which may be due to the siliceous nature of the particulate phase in circumpolar waters. Our previous observation that the210Pb/226Ra activity ratio is of the order of 0.5 in the deep water is further confirmed by the two South Atlantic profiles analyzed in the present work.  相似文献   

19.
210Pb is widely used for dating recent sediments in the aquatic environment; however, our experiences working in shallow coastal environments in the Pacific coast of Mexico have demonstrated that the potential of 210Pb for reliable historical reconstructions might be limited by the low 210Pb atmospheric fallout, sediment mixing, abundance of coarse sediments and the lack of 137Cs signal for 210Pb corroboration. This work discusses the difficulties in obtaining adequate sedimentary records for geochronological reconstruction in such active and complex settings, including examples of 210Pb geochronologies based on sediment profiles collected in two contrasting areas coastal areas (mudflats associated to coastal lagoons of Sinaloa State and the continental shelf of the Gulf of Tehuantepec), in which geochemical data was used to support the temporal frame established and the changes in sediment supply recorded in the sediment cores which were related to the development of land-based activities during the last century.  相似文献   

20.
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.  相似文献   

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